SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs232056 | snp | C/T | 0.334871 | 0.235153 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27475248 | AAGCCCAAGCCCTAT[C/T]CTCAGAGACTCCAGT | 2975 |
rs232057 | snp | C/T | 0.228842 | 0.249103 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27476873 | TTTCTCACTGAAATA[C/T]AGAGCTAAAATCAAA | 2975 |
rs232058 | snp | A/G | 0.229136 | 0.249128 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27477551 | ctcaggtgatccgcc[A/G]gcagcgccctcccaa | 2975 |
rs232059 | snp | A/G | 0.126909 | 0.217598 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27480668 | TAAGATTTAAAAATT[A/G]TACAGGGTTCTGTGC | 2975 |
rs232060 | snp | C/T | 0.241914 | 0.249869 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27480709 | GATTCTTCTTCCAAA[C/T]GCCGAGTGGTTACAG | 2975 |
rs232061 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27483180 | AATGATGCCCATGTT[A/C]AGAACCTTCAGAGAG | 2975 |
rs232062 | snp | C/T | 0.192374 | 0.243268 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27483354 | GGCTTCTCTGAACTT[C/T]CGTCCTTCATAGGTA | 2975 |
rs232063 | snp | A/C | 0.25634 | 0.24992 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27483972 | TCCAAAAAAAGGATA[A/C]CACCACCTACTTCTC | 2975 |
rs232064 | snp | A/T | 0.240478 | 0.249819 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27487412 | GACACTGGTCTCCTT[A/T]CCACTCCCTCTGCTA | 2975 |
rs232065 | snp | A/C | 0.243347 | 0.249911 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27488040 | TGGCAGATGAGAGAG[A/C]CTCGAATATCCCGTA | 2975 |
rs232066 | snp | A/G | 0.33303 | 0.235809 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27488712 | AGTAACAAATGCACC[A/G]AGGTCTCTTAGGAAG | 2975 |
rs232067 | snp | C/T | 0.264874 | 0.263799 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27489868 | GCTCCCCGGCCACTG[C/T]GGGGGTCTGAGATTG | 2975 |
rs232068 | snp | G/T | 0.245061 | 0.249951 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27491100 | CGTATTTTAGAACAG[G/T]GTGTTTCATAGAATC | 2975 |
rs232069 | snp | A/G | 0.330016 | 0.236849 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27494184 | agacgggcggatcac[A/G]aggtcagaagattga | 2975 |
rs232070 | snp | C/T | 0.32955 | 0.237006 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27494236 | aaaaccccgtctcta[C/T]taaaaatataaaaaa | 2975 |
rs232071 | snp | A/G | 0.262937 | 0.249665 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27495504 | GGAACTAAAGCAAGA[A/G]AGGGAGAGGGCGGTG | 2975 |
rs232072 | snp | C/T | 0.135324 | 0.223778 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27501439 | CCTCACGGTACCCAA[C/T]AGAAACAAGGAAGGA | 2975 |
rs232073 | snp | A/G | 0.243919 | 0.249926 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27502538 | TCCATAGCCCTTCTG[A/G]AGCAACCATCTTCCA | 2975 |
rs232074 | snp | C/T | 0.331642 | 0.236293 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27504031 | GGGCAGAAAGTCTTT[C/T]GTTCACCTTCGTGCT | 2975 |
rs232075 | snp | C/T | 0.261056 | 0.249755 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27504430 | CAGGCCTTTTCTATT[C/T]ATTGGATGCCACAAC | 2975 |
rs232076 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27507248 | CTATTTCCTTATTGG[C/G]TTTCTTCTGTTTCTC | 2975 |
rs232077 | snp | C/G | 0.261608 | 0.24973 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27507574 | GCCATGAGGATTTGT[C/G]GACTGGGCATCAGTG | 2975 |
rs232078 | snp | C/T | 0.128288 | 0.218372 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27510094 | tctctactaaagaaa[C/T]agaaaattagtccgg | 2975 |
rs232079 | snp | A/G | 0.261884 | 0.249717 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27511987 | GAAATATCACAGCAC[A/G]TGTCAGCAGAGACAG | 2975 |
rs232080 | snp | A/C | 0.406641 | 0.194842 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27516491 | GGGCATAGCTGATTT[A/C]TCTGCTGTGAATCCC | 2975 |
rs232081 | snp | A/T | 0.230603 | 0.249246 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27517859 | TGGTCATGTGATCTA[A/T]CCGATGCCTTCCACA | 2975 |
rs232082 | snp | C/T | 0.242775 | 0.249896 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27520782 | tggagaacagaggtg[C/T]gatctcagctcactg | 2975 |
rs232083 | snp | A/G | 0.261608 | 0.24973 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27522647 | gtggaggagtcagtc[A/G]ggattctcacacgga | 2975 |
rs232084 | snp | A/G | 0.230017 | 0.2492 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27523633 | GCTCAGCATCTGCTT[A/G]GCACCTACTCTGTTC | 2975 |
rs232085 | snp | A/G | 0.291235 | 0.246576 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27525261 | ACACCTCTCAGTTCC[A/G]TGAGCCTTTTTTCTT | 2975 |
rs232086 | snp | A/T | 0.44858 | 0.151875 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27525875 | GCTTGGTTTTCTATG[A/T]GCATGTCACTAACTC | 2975 |
rs232087 | snp | A/G | 0.227959 | 0.249026 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27528200 | gaattgcttgaaccc[A/G]aaaggcagaggttgt | 2975 |
rs232088 | snp | A/G | 0.228842 | 0.249103 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27528230 | tagtgagcagagatc[A/G]caccactgcactatg | 2975 |
rs963664 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27547851 | ACTGGTCTTGAACTC[C/T]TGACCTCAAGTTATC | 2975 |
rs963665 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27547858 | TTGAACTCCTGACCT[C/T]AAGTTATCCGCCCAC | 2975 |
rs1134711 | snp | C/T | 0.228253 | 0.249052 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27539133 | AAATATACACAGAGC[C/T]CCTATTATCACCCAA | 2975 |
rs1609758 | snp | A/G | 0.249603 | 0.25 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27543635 | caaggcaggaggatc[A/G]cttgaggctgggagt | 2975 |
rs1609759 | snp | A/G | 0.332337 | 0.236052 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27543505 | tacttgggagactgc[A/G]atggggggattgctt | 2975 |
rs2228248 | snp | A/G | 0.213275 | 0.247288 | missense | GTF3C1 | GRCh38.p7 | 16:27461451 | CCCTCCAGCCTGGAC[A/G]AGAGCCCCATGGCTT | 2975 |
rs2228249 | snp | A/T | 0.0012231 | 0.0246993 | missense, upstream-variant-2KB | GTF3C1, KIAA0556 | GRCh38.p7 | 16:27549716 | CACCCGGGCATCAGC[A/T]TCTATGAGGAGCCTC | 2975 |
rs2229355 | snp | A/G/T | 0.00326023 | 0.0402451 | missense | GTF3C1 | GRCh38.p7 | 16:27469309 | TGCACCCCTGTGCCC[A/G/T]CCCGGCTCAGGCCCG | 2975 |
rs2238523 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27530795 | TTCATCGTGGGGGCC[C/T]GCAGTGAGCAAGCAG | 2975 |
rs2283559 | snp | C/T | 0.0995161 | 0.199636 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27496241 | ACCATGCTTCCTATA[C/T]AGCCTGTAGAACTGT | 2975 |
rs2382868 | snp | C/T | 0.0209421 | 0.100162 | intron-variant, upstream-variant-2KB | GTF3C1, KIAA0556 | GRCh38.p7 | 16:27548579 | cTGTCTTGGACATTA[C/T]TACCTCTTGGAACCT | 2975 |
rs3760092 | snp | C/T | 0.00716266 | 0.059414 | upstream-variant-2KB, intron-variant | GTF3C1, KIAA0556 | GRCh38.p7 | 16:27550762 | TTAACACCTCTGAGC[C/T]TCAGTTTCATCATCT | 2975 |
rs3785355 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27497183 | ATTTCTAAACTTGTG[C/G]TGAACAAGGCAGGTG | 2975 |
rs3842364 | in-del | -/C | 0.408871 | 0.193029 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27491735 | TAGGAGGAGAGTGGC[-/C]GTCCACTGGTGACAG | 2975 |
rs4787962 | snp | C/T | 0.173965 | 0.238157 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27477417 | GATCAAGCGATTCTC[C/T]TGCCTCAGCCTCCCC | 2975 |
rs4787963 | snp | A/C | 0.270892 | 0.249126 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27483556 | TCACATCTCCATGAT[A/C]TAAGGAGAGCCTGAC | 2975 |
rs4787964 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27527958 | cagcctgggcaacag[A/G]gaaagaccctgtctc | 2975 |
rs4787965 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27540016 | ACCAATTCTGTTCAC[C/T]GGGAGCCAACATCCA | 2975 |
rs4787966 | snp | A/G | 0.241914 | 0.249869 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27547051 | ccagcccaaccctcc[A/G]ttcttaaatgatcct | 2975 |
rs4787967 | snp | C/G | 0.332337 | 0.236052 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27547238 | tacactctctcttag[C/G]gctgatcttagccag | 2975 |
rs4787968 | snp | C/T | 0.127254 | 0.217792 | intron-variant, upstream-variant-2KB | GTF3C1, KIAA0556 | GRCh38.p7 | 16:27548494 | cgggtcttgaactgc[C/T]gaccttgtgacccat | 2975 |
rs4787969 | snp | A/G | 0.238171 | 0.24972 | upstream-variant-2KB, intron-variant | GTF3C1, KIAA0556 | GRCh38.p7 | 16:27550263 | AGAATCCTAGGCCAT[A/G]AACCCCTGGACCACC | 2975 |
rs5816438 | in-del | -/T | 0.313326 | 0.241847 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27544975 | GAATTTCTTTTTTCC[-/T]TTTTTTTTTTTTTTG | 2975 |
rs7185518 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27538998 | cacacacacacacac[A/T]ctcatcttttttttt | 2975 |
rs7188070 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27525125 | aactgcactccagcc[G/T]gggcaatagagagaa | 2975 |
rs7188677 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27499473 | GTCTCTGCTGAGGCC[A/G]GGGACAGCAAGGTCA | 2975 |
rs7189110 | snp | C/T | 0.0168128 | 0.0901316 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27493931 | atagtttcaattcag[C/T]ttttttttttaaagg | 2975 |
rs7190780 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27494070 | acagttatgggtaat[C/T]tctattttatctttc | 2975 |
rs7198199 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27513145 | gattatctgggtggg[C/G]tcaatgtagtatcac | 2975 |
rs7198785 | snp | C/T | 0.332337 | 0.236052 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27546428 | AACACCATGGAGACA[C/T]TTTTCATTTGTGCTT | 2975 |
rs7199317 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27461949 | GAGGAGCTGGAGGCC[C/T]CAGGCACACATGGGA | 2975 |
rs7200706 | snp | A/T | 0.2462 | 0.249971 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27541414 | GTCAGGGGTTACAAC[A/T]TCAAACATGTATTTC | 2975 |
rs7201382 | snp | C/T | 0.143284 | 0.226079 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27529214 | TTTGGGAGGCCGAGG[C/T]GGGCAGGTCACTTAA | 2975 |
rs7204957 | snp | G/T | 0 | 0 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27541753 | AGGCTGAAGTGCAGT[G/T]CAGAGTGAAGAAACT | 2975 |
rs7359485 | snp | C/T | 0 | 0 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27492843 | CACTGGAGGACCAGC[C/T]TCAAGCCCACACTGC | 2975 |
rs8053192 | snp | A/G | 0.333261 | 0.235728 | intron-variant, upstream-variant-2KB | GTF3C1, KIAA0556 | GRCh38.p7 | 16:27549565 | AATCAACAGGCCTCC[A/G]GTACTTGCACAGCCC | 2975 |
rs8056549 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27467304 | aaatctattctgcct[C/G]tgctctataaacaga | 2975 |
rs8061750 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27505443 | ttctaacctctccct[A/G]ttggatgccagtagc | 2975 |
rs8061947 | snp | C/T | 0.229136 | 0.249128 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27546852 | gctcactgcaacctc[C/T]accttctgggttcaa | 2975 |
rs9788850 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27475047 | GGCATTCAAGCCCAG[C/T]GTGGCATTTTCCTGA | 2975 |
rs9888849 | snp | C/T | 0.264084 | 0.249603 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27464978 | GGCAGGCCTGGCTCC[C/T]AGCCCCGGGGCTGCC | 2975 |
rs9924603 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27513639 | TCTTCTAAAGCCTCC[A/G]GAAGGAACACTGCCC | 2975 |
rs9926802 | snp | A/G | 0.00478139 | 0.0486604 | upstream-variant-2KB | GTF3C1, KIAA0556 | GRCh38.p7 | 16:27549941 | CAACGCACCGCCAAG[A/G]GCCTTGGTCCATCGC | 2975 |
rs9928940 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27468457 | tctctacaaaaaatt[A/T]aaaaattagctggct | 2975 |
rs9932408 | snp | A/G | 0 | 0 | upstream-variant-2KB, intron-variant | GTF3C1, KIAA0556 | GRCh38.p7 | 16:27551731 | ctctactaaaactta[A/G]ccggacgtggtgaca | 2975 |
rs9933281 | snp | A/G | 0.228547 | 0.249078 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27539795 | TGGGTTAGTTATCTC[A/G]GGAGTGGGACGTCCT | 2975 |
rs9938472 | snp | A/G | 0 | 0 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27466508 | gctccctattcctga[A/G]acacaacaatattga | 2975 |
rs10658820 | in-del | -/TT | 0.0221141 | 0.102801 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27525951 | AGTATCCTATGTTTG[-/TT]TTTCTTATGAGTTTT | 2975 |
rs10852319 | snp | C/T | 0.332337 | 0.236052 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27536785 | TTCCTCAGCTAAGGG[C/T]TGCTCTTCCCAGGCC | 2975 |
rs11406778 | in-del | -/A | 0.372391 | 0.217992 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27546486 | GTTTTTTTTTTTTTG[-/A]AAAAAAAAAAAAAAT | 2975 |
rs11452553 | in-del | -/A | 0.409721 | 0.192325 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27498796 | AAGACTTGGCTCCAC[-/A]AGTCGATTCCTAGTG | 2975 |
rs11551766 | snp | A/G | | | synonymous-codon | GTF3C1 | GRCh38.p7 | 16:27469460 | CCGGAGCATGGAGGT[A/G]AAACCTGCGCAAGCC | 2975 |
rs11639882 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27512881 | acagcttgtaagtgA[C/T]GGGAAAAATGACTCA | 2975 |
rs11642654 | snp | A/C | 0.00392926 | 0.0441496 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27514540 | CCATGCCATTCCCCC[A/C]TAGACTGTCCTCTAG | 2975 |
rs11642951 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27536289 | tagtagttaagtttt[G/T]ggggagtcaaaagtt | 2975 |
rs11644385 | snp | C/T | 0 | 0 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27546395 | TCTTACTACCGCTTT[C/T]TTCCATGTGCCTCTT | 2975 |
rs11644860 | snp | C/G | 0 | 0 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27496800 | CTGTGAGAGGAGGTA[C/G]GCACAGCAAGAGGGT | 2975 |
rs11648096 | snp | A/G | 0.0825414 | 0.185628 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27493565 | TAAACCTTTCCCGGG[A/G]GCAACATAAGAATAT | 2975 |
rs11860944 | snp | A/G | 0 | 0 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27474228 | GAGGGAGGCTACGCA[A/G]GCCGGTGGTCTTTCT | 2975 |
rs11861368 | snp | C/T | 0.0102561 | 0.0708723 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27510947 | CTTCTTCTCAGTGCT[C/T]TCTATGCACCAGGCC | 2975 |
rs11864254 | snp | A/G | | | intron-variant | GTF3C1 | GRCh38.p7 | 16:27510145 | aatcccagcacttta[A/G]gaggccgaggcaggt | 2975 |
rs12445469 | snp | A/C | | | intron-variant | GTF3C1 | GRCh38.p7 | 16:27477971 | ggccaggagttccag[A/C]ccagcctggccaaca | 2975 |
rs12445494 | snp | C/T | 0.224412 | 0.248687 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27477987 | ccagcctggccaaca[C/T]ggcaaaaccccgtct | 2975 |
rs12445873 | snp | A/G | 0.243633 | 0.249919 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27462893 | CAGAGTTCCAGGCAC[A/G]CTTTCCTCGAAACAG | 2975 |
rs12448389 | snp | C/T | 0.444444 | 0.157135 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27546891 | cctgcctcagcctcc[C/T]tagtagctgggatca | 2975 |
rs12919017 | snp | A/G | 0.213408 | 0.247308 | missense | GTF3C1 | GRCh38.p7 | 16:27463589 | CCGAAACTCTCTGTG[A/G]ACCCTGAGGGAAGAG | 2975 |
rs12919042 | snp | C/T | 0.232067 | 0.249356 | intron-variant | GTF3C1 | GRCh38.p7 | 16:27468807 | AAAATAGTGTCAAAA[C/T]TGGAAGTAAAGGAGG | 2975 |