SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1050827 | snp | C/G | 0 | 0 | missense, intron-variant, upstream-variant-2KB | G6PD, IKBKG | GRCh38.p7 | X:154546123 | CCTGAGCCGGACCCA[C/G]GTGTGCGGGATCCTG | 8517 |
rs2472393 | snp | C/T | 0.484855 | 0.0856918 | intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154543081 | GGCGTGGAAGAAGCC[C/T]GGGAGCCGGAGCTGT | 8517 |
rs2472394 | snp | A/C | 0.264457 | 0.249582 | intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154543136 | CCTCCCATCTCCCCC[A/C]CAGCAGGAAGAGGAA | 8517 |
rs2515903 | snp | G/T | 0 | 0 | upstream-variant-2KB, intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154548417 | GCCCACTATGGTCTG[G/T]TCTCCCCACCACTGC | 8517 |
rs2515910 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154543369 | CCCAGGGTCCTTAGG[C/T]TTTTCCAAGCTGATT | 8517 |
rs3021072 | snp | G/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154547145 | AGTAGGGGCGGGGCC[G/T]GGCCGGCGATGGGGA | 8517 |
rs3021073 | snp | G/T | | | upstream-variant-2KB, intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154547134 | GGCCGGGCCGGCGAT[G/T]GGGATGCGGGAGCAC | 8517 |
rs3021074 | snp | G/T | 0 | 0 | upstream-variant-2KB, intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154547128 | GCCGGCGATGGGGAT[G/T]CGGGAGCACTACGCG | 8517 |
rs4898387 | snp | A/G | | | | | GRCh38.p7 | X:154568154 | AACAGCAAGTCTGAC[A/G]GCAAGCAAAAAGTGA | 8517 |
rs5945207 | snp | G/T | | | | | GRCh38.p7 | X:154567887 | AGTACGGCATTCCAG[G/T]GTTTTCCTTTTCGGC | 8517 |
rs5986992 | snp | A/C | 0.0199298 | 0.0978146 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | G6PD, IKBKG | GRCh38.p7 | X:154547892 | CTGGCCAAGGCGGGC[A/C]GATTCAGGACCCAGG | 8517 |
rs5986993 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | IKBKG | GRCh38.p7 | X:154553152 | GGGACTCAGGCCTAA[A/G]TGTCCACCCCATCGT | 8517 |
rs6643680 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | IKBKG | GRCh38.p7 | X:154553661 | gagaattctcttgta[C/T]gttgtagggtgtgga | 8517 |
rs7064060 | snp | C/T | 0.0168099 | 0.0901243 | intron-variant, upstream-variant-2KB | G6PD, IKBKG | GRCh38.p7 | X:154545783 | gaggttgcagtgagc[C/T]aagatggcgccactg | 8517 |
rs7066099 | snp | C/G | 0.0168099 | 0.0901243 | upstream-variant-2KB, intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154549568 | tacaggtgtgaacca[C/G]catgcctggccACCA | 8517 |
rs11544439 | snp | A/G | | | intron-variant, missense | G6PD, IKBKG | GRCh38.p7 | X:154542396 | CCATCAGGTGGGGAA[A/G]GATGCTGTTCCAGGC | 8517 |
rs11797720 | snp | C/T | 0 | 0 | intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154545224 | AGTGCAGAATGGCGG[C/T]TCTACAAGCTGGACA | 8517 |
rs12837628 | snp | C/G | | | upstream-variant-2KB, intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154549350 | gatcttggctcaccg[C/G]aacctccatctccca | 8517 |
rs12847690 | snp | A/G | | | upstream-variant-2KB, intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154547205 | TCGCGCGCTCGCGGA[A/G]GGCTCCACTTCCGCC | 8517 |
rs12850218 | snp | A/T | | | upstream-variant-2KB, intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154547204 | CTCGCGCGCTCGCGG[A/T]GGGCTCCACTTCCGC | 8517 |
rs12861291 | snp | C/G | 0 | 0 | intron-variant | IKBKG | GRCh38.p7 | X:154550639 | gggcaggagtagcca[C/G]caagatagggaggaa | 8517 |
rs34585701 | in-del | -/C | | | intron-variant | IKBKG | GRCh38.p7 | X:154549740 | CAGCTTATCTTCCCC[-/C]TCAGCCCTAAGTGGC | 8517 |
rs34859682 | in-del | -/A | | | intron-variant, upstream-variant-2KB | G6PD, IKBKG | GRCh38.p7 | X:154540656 | AAAAAAAAAAAAAAA[-/A]CACATGCTCTTCGAA | 8517 |
rs35948381 | in-del | -/T | | | intron-variant, upstream-variant-2KB | G6PD, IKBKG | GRCh38.p7 | X:154540899 | GTGCCAGGACTACAG[-/T]CGACACGGACCTCTC | 8517 |
rs55905799 | in-del | -/T | | | intron-variant | IKBKG | GRCh38.p7 | X:154551129 | TTTTTTTTTTTTTTT[-/T]AGTAGAGGCAGGGTT | 8517 |
rs56191948 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | G6PD, IKBKG | GRCh38.p7 | X:154547875 | TCCGCGCTTCTGGAG[C/T]ACTGGCCAAGGCGGG | 8517 |
rs56262786 | snp | C/G | 0.0348667 | 0.127349 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | G6PD, IKBKG | GRCh38.p7 | X:154547940 | TGGACTGTTTCTACT[C/G]CTCCCTCCTCCTCCA | 8517 |
rs57174646 | snp | A/C | 0.00291275 | 0.0380511 | synonymous-codon | IKBKG | GRCh38.p7 | X:154552009 | CCCTGTTGGATGAAT[A/C]GGCACCTCTGGAAGA | 8517 |
rs60589782 | snp | C/T | 0.0425 | 0.139441 | upstream-variant-2KB, intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154549184 | GATGGGGTTTCATCA[C/T]GTTGGCCAGGATGGT | 8517 |
rs60738129 | snp | G/T | 0.0650211 | 0.168175 | intron-variant | G6PD | GRCh38.p7 | X:154539884 | CCTGCCACCACGCCC[G/T]GCTAATTTTTGTATT | 8517 |
rs61120457 | snp | A/T | | | intron-variant | IKBKG | GRCh38.p7 | X:154550277 | GTGTGTGTGTGTGTG[A/T]GAGAGAGAGAGAGAG | 8517 |
rs61309512 | snp | A/G | 0.0379276 | 0.132383 | intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154544533 | CTCCTGACCTCAGGC[A/G]ATCCACCTGCCTCGG | 8517 |
rs73573488 | snp | A/G | 0.181482 | 0.240427 | intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154542910 | TAGCACATAGGTCCC[A/G]TGAGGAGGGCAGGGA | 8517 |
rs73641103 | snp | A/G | 0.0068637 | 0.0581785 | intron-variant, upstream-variant-2KB | G6PD, IKBKG | GRCh38.p7 | X:154541674 | TCTCATCTTCCCCAC[A/G]CCCTCCTCTTTCCTG | 8517 |
rs73641104 | snp | G/T | 0.0379276 | 0.132383 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | G6PD, IKBKG | GRCh38.p7 | X:154547962 | CCTCCTCCACTGCGG[G/T]GTCTGACCCTACTCC | 8517 |
rs73641105 | snp | C/T | 0.0389457 | 0.134 | intron-variant | IKBKG | GRCh38.p7 | X:154551724 | CTCCACAAACAGTCT[C/T]GTCCCGACTCTCCCA | 8517 |
rs75328199 | snp | A/G | | | upstream-variant-2KB, intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154549564 | GGATTACAGGTGTGA[A/G]CCACCATGCCTGGCC | 8517 |
rs76866072 | snp | G/T | 0 | 0 | intron-variant | IKBKG | GRCh38.p7 | X:154555597 | TTTTTTTCTTTTTTT[G/T]GAGACAGAGTTTTGC | 8517 |
rs77108259 | snp | A/G | 0.5 | 0 | intron-variant | IKBKG | GRCh38.p7 | X:154551318 | AAGCACACACCCTCA[A/G]AGGCTCTAAGAGGGC | 8517 |
rs111267224 | snp | C/T | 0.0525796 | 0.153379 | upstream-variant-2KB, intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154548132 | CGTTTTGCAAGACAA[C/T]ATCTGCCTATCGTCA | 8517 |
rs111314857 | snp | G/T | | | | | GRCh38.p7 | X:154568636 | TTTCCTTACATGTTA[G/T]TACCTTTCCTAAATG | 8517 |
rs111583550 | snp | C/G | | | intron-variant | IKBKG | GRCh38.p7 | X:154555668 | CACTGCAACCTCCAC[C/G]TCCCAGGTTCAAGTG | 8517 |
rs111615979 | snp | C/T | 0.0555816 | 0.157167 | intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154542980 | TCAATGAACGGAGAA[C/T]GGGCTGCTTTCCTGG | 8517 |
rs111827785 | snp | C/T | 0.238698 | 0.249744 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154547570 | CGGCTTCCCGAGTTC[C/T]CGGGGGCGGGGCTTG | 8517 |
rs111835688 | snp | A/G | | | upstream-variant-2KB, intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154549140 | GTTGTGCACCACCAC[A/G]CCCAGCTAATTTTTG | 8517 |
rs111886710 | snp | C/T | | | intron-variant | IKBKG | GRCh38.p7 | X:154552949 | CTCCCTGCCACTGCT[C/T]TGCATTGCCCTGGGT | 8517 |
rs111972091 | snp | C/T | | | upstream-variant-2KB, intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154549139 | AGTTGTGCACCACCA[C/T]GCCCAGCTAATTTTT | 8517 |
rs112022908 | snp | C/T | 0.0353775 | 0.128208 | intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154543105 | GAGCTGTTCCAGGTG[C/T]TGCCTGAGCACGCCA | 8517 |
rs112883659 | snp | A/G | | | | | GRCh38.p7 | X:154565620 | AGGCAGGTGGATCAC[A/G]TGAGGTCAGGAGTTC | 8517 |
rs112921384 | snp | G/T | | | intron-variant, upstream-variant-2KB | G6PD, IKBKG | GRCh38.p7 | X:154545874 | CTTGCAAGTGCATAT[G/T]CACACCAGGTAGAGC | 8517 |
rs112939849 | snp | C/G | | | | | GRCh38.p7 | X:154567117 | TTCTTTCTTTTCTTT[C/G]TCCCTCTCTCTCTCC | 8517 |
rs112987151 | snp | A/T | | | intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154544567 | CCCAAAGTGCTGGGA[A/T]TACAGGCGTGAGCCA | 8517 |
rs113161481 | snp | G/T | | | intron-variant | IKBKG | GRCh38.p7 | X:154555761 | ATTTTTGTATTTTTA[G/T]TAGAGACGGGGTTTC | 8517 |
rs113233572 | snp | C/T | | | intron-variant | IKBKG | GRCh38.p7 | X:154561351 | CGTTTTCCTATGTTG[C/T]CCGGGCTGGTCTTGA | 8517 |
rs113293478 | snp | A/G | | | downstream-variant-500B | IKBKG | GRCh38.p7 | X:154565358 | TATAGTTGTGTATAT[A/G]TATGTGTGTGTGTGT | 8517 |
rs113492957 | snp | C/T | 0.054582 | 0.155922 | intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154544847 | GACAAAGTGTGACAG[C/T]GCGTTGTTCTATGTG | 8517 |
rs113568108 | snp | A/G | | | intron-variant, upstream-variant-2KB | G6PD, IKBKG | GRCh38.p7 | X:154545601 | GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC | 8517 |
rs113796767 | snp | G/T | 0.00738971 | 0.0603345 | upstream-variant-2KB, intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154548155 | TATCGTCATACTGTT[G/T]CTGTGATCTGAGAAT | 8517 |
rs113807442 | snp | A/G | 0.00791544 | 0.0624105 | intron-variant | IKBKG | GRCh38.p7 | X:154551170 | AGCCAGGCTGGTCTC[A/G]ATCTCCTGACCTCAT | 8517 |
rs113881586 | snp | C/G | | | intron-variant | G6PD | GRCh38.p7 | X:154540043 | TATATTTCAATAAAA[C/G]ATGGTAAAAACTAAT | 8517 |
rs113953174 | snp | A/G | | | intron-variant | IKBKG | GRCh38.p7 | X:154554569 | TTTGAGACCAGCTTG[A/G]CCAACATGGTGAAAC | 8517 |
rs137852338 | in-del | -/ATC | | | cds-indel, intron-variant, upstream-variant-2KB | G6PD, IKBKG | GRCh38.p7 | X:154546051 | GATACACACATATTC[-/ATC]ATCATGGGTGCATCG | 8517 |
rs137852340 | snp | A/G | 0.000274295 | 0.0117078 | G6PD, IKBKG | X | allele_origin=G(germline)/A(germline) | X:154546061 | ATCAGTCGGATACAC[A/G]CATATTCATCATCAT | 8517 |
rs137853321 | snp | A/G | | | stop-lost | IKBKG | GRCh38.p7 | X:154564460 | TGGAGTGCATTGAGT[A/G]GGGCCGGCCAGTGCA | 8517 |
rs137853322 | snp | A/G | 0.00191938 | 0.0309194 | IKBKG | X | allele_origin=G(germline)/A(germline) | X:154564420 | TATCAGGCCCCTGAT[A/G]TGGACACCCTGCAGA | 8517 |
rs137853323 | snp | C/T | | | stop-gained | IKBKG | GRCh38.p7 | X:154552186 | GAGAATCAAGAGCTC[C/T]GAGGTGAGGAAAGAG | 8517 |
rs137853324 | snp | G/T | | | stop-gained | IKBKG | GRCh38.p7 | X:154564372 | AGGAGCCCCCCCGAG[G/T]AGCCACCTGACTTCT | 8517 |
rs137853325 | snp | C/T | | | missense | IKBKG | GRCh38.p7 | X:154564450 | ATACATGTCATGGAG[C/T]GCATTGAGTAGGGCC | 8517 |
rs137853326 | snp | A/G/T | | | missense | IKBKG | GRCh38.p7 | X:154564451 | TACATGTCATGGAGT[A/G/T]CATTGAGTAGGGCCG | 8517 |
rs137853327 | snp | A/T | | | missense | IKBKG | GRCh38.p7 | X:154564418 | AGTATCAGGCCCCTG[A/T]TATGGACACCCTGCA | 8517 |
rs137853328 | snp | G/T | | | missense | IKBKG | GRCh38.p7 | X:154558590 | CCTTGCTCGGGGAGC[G/T]GCAGGAGAGCCAGAG | 8517 |
rs137853329 | snp | C/T | | | stop-gained | IKBKG | GRCh38.p7 | X:154564408 | CCCAAGTGCCAGTAT[C/T]AGGCCCCTGATATGG | 8517 |
rs137853330 | snp | C/G | | | missense, intron-variant | IKBKG | GRCh38.p7 | X:154562904 | AGCTGAAGGAGGAGG[C/G]CGAGCAGCACAAGAT | 8517 |
rs137853331 | snp | A/C | | | missense | IKBKG | GRCh38.p7 | X:154563590 | CGGACTTCCAGGCTG[A/C]GAGGCAGGCCCGGGA | 8517 |
rs137853332 | snp | A/G | | | missense | IKBKG | GRCh38.p7 | X:154563602 | CTGAGAGGCAGGCCC[A/G]GGAGAAGCTGGCCGA | 8517 |
rs140446617 | snp | C/T | 0.0485612 | 0.148062 | intron-variant | IKBKG | GRCh38.p7 | X:154553216 | CCTGAGCTGGCAGCT[C/T]CAATTGGCTCTCCGT | 8517 |
rs142579132 | snp | A/G | 0.0194105 | 0.0965841 | intron-variant | IKBKG | GRCh38.p7 | X:154551208 | CCGCCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC | 8517 |
rs143277699 | snp | A/G | 0.054582 | 0.155922 | upstream-variant-2KB, intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154549317 | CACTCTGTCGCCCAG[A/G]ATGGAGTGCAGTGGC | 8517 |
rs143379366 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | IKBKG | GRCh38.p7 | X:154552342 | GATTAGCGGGGAGGA[A/T]GTTTAGCATGCTCTC | 8517 |
rs143636168 | snp | C/G | 0.0550819 | 0.156547 | intron-variant | IKBKG | GRCh38.p7 | X:154555465 | TAATCCCAGCACTTT[C/G]GGAGGCCGAGGTGGG | 8517 |
rs143999678 | snp | A/G | 0.000188985 | 0.00971888 | missense | IKBKG | GRCh38.p7 | X:154552141 | CCTTCAGAACAGGGC[A/G]CTCCTGAGACCCTCC | 8517 |
rs144228258 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154543529 | AGTCATAAGCTATCA[C/T]TGTGGCCTGGGTTGC | 8517 |
rs144918804 | snp | C/T | 0.0287145 | 0.11633 | intron-variant, upstream-variant-2KB | G6PD, IKBKG | GRCh38.p7 | X:154545801 | GATGGCGCCACTGCA[C/T]CCCATCCTGGGCGAC | 8517 |
rs145036913 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154545311 | AAGAGACAGTGTTCA[A/G]AGAAAAGCTAAGTGT | 8517 |
rs145722968 | snp | C/T | 0.0105399 | 0.0718252 | intron-variant | IKBKG | GRCh38.p7 | X:154554389 | ACCTGATGGATACAC[C/T]GAAAACTGCTGAATT | 8517 |
rs146051477 | snp | A/G | 0.00844089 | 0.0644143 | intron-variant | G6PD | GRCh38.p7 | X:154539216 | ACCTGCACACGAATG[A/G]TCACAGCAGCCTTGG | 8517 |
rs146713404 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | IKBKG | GRCh38.p7 | X:154553163 | CTAAGTGTCCACCCC[A/G]TCGTGGAGGACAACA | 8517 |
rs148118581 | snp | C/T | 0.0485612 | 0.148062 | intron-variant | IKBKG | GRCh38.p7 | X:154555724 | AGCTGGGATTACAGG[C/T]GTGTGCCACCACACC | 8517 |
rs148695964 | snp | A/G | 0.00237672 | 0.0343906 | IKBKG | X | allele_origin=G(germline)/A(germline) | X:154552171 | CAGCGCTGCCTGGAG[A/G]AGAATCAAGAGCTCC | 8517 |
rs148924418 | snp | A/G | 0.0550819 | 0.156547 | intron-variant | IKBKG | GRCh38.p7 | X:154554508 | TCATGCCTGTAATCC[A/G]AGCACTTTGGGAGGC | 8517 |
rs149511938 | snp | C/T | 0.00047235 | 0.0153607 | synonymous-codon | IKBKG | GRCh38.p7 | X:154552140 | GCCTTCAGAACAGGG[C/T]GCTCCTGAGACCCTC | 8517 |
rs149618083 | snp | C/T | 0.00370173 | 0.0428621 | upstream-variant-2KB, intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154548594 | TGAGAGATGGAGTCT[C/T]GCTCTGTCGCCCAGG | 8517 |
rs149902811 | snp | A/C | 0.0328205 | 0.123827 | intron-variant | G6PD, IKBKG | GRCh38.p7 | X:154544945 | TAGAGCTCCTGCTCA[A/C]GGTTACAAGGTAAGT | 8517 |
rs150358028 | snp | A/G | 0.22669 | 0.248911 | intron-variant | IKBKG | GRCh38.p7 | X:154553820 | GTATTGGGATCTTCA[A/G]AGCACTGGTGCACAG | 8517 |
rs179363865 | snp | C/G | | | missense | IKBKG | GRCh38.p7 | X:154563613 | GCCCGGGAGAAGCTG[C/G]CCGAGAAGAAGGAGC | 8517 |
rs179363866 | snp | C/G | | | missense | IKBKG | GRCh38.p7 | X:154558649 | CAGGCTCTGGAGGGT[C/G]GGTGAGTCGGGGGAG | 8517 |
rs179363867 | snp | A/G | | | missense | IKBKG | GRCh38.p7 | X:154563577 | GATATCTACAAGGCG[A/G]ACTTCCAGGCTGAGA | 8517 |
rs179363868 | snp | C/G | | | missense, intron-variant | IKBKG | GRCh38.p7 | X:154560412 | CCCGTGCCAGGGCCC[C/G]GGCGGCCAGCGAGCA | 8517 |
rs179363869 | snp | C/T | | | missense | IKBKG | GRCh38.p7 | X:154561696 | TCCTCAGGAGGAAGC[C/T]GGCCCAGTTGCAGGT | 8517 |
rs179363895 | snp | C/T | | | missense | IKBKG | GRCh38.p7 | X:154556344 | AAGGAGCAGGCTCTG[C/T]GGGAGGTGGAGCACC | 8517 |