SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs721896 | snp | A/T | 0.0391387 | 0.134304 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923166 | gacaaggtctagctg[A/T]gttgcccaggctgga | 388795 |
rs871103 | snp | C/T | 0.282632 | 0.247861 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893470 | GCTGCCCCCCATCGC[C/T]TCTCCCTCTGTGCTG | 388795 |
rs871104 | snp | C/T | 0.265727 | 0.249505 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893721 | CATCCAGGACAGCCC[C/T]TGCCCACCCAAAGGC | 388795 |
rs967475 | snp | G/T | 0.233235 | 0.249437 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943363 | CATATGCAAGTCATA[G/T]GCAAGTCATATGTAG | 388795 |
rs1000618 | snp | C/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902930 | TGACCCCCGGCGTCT[C/G]CCCGACTGTCCCCTC | 388795 |
rs1116583 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951145 | gcattttggcagttt[C/T]ttaaaaagttaaatg | 388795 |
rs1181342 | snp | G/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921295 | ACTCCTGGGCTGAAG[G/T]GACCCTCCCACCTCA | 388795 |
rs1181343 | snp | A/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921329 | TTGTGAGTAGCTGGG[A/G]CTATAGGCATGCTCC | 388795 |
rs1181344 | snp | A/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921342 | GGGCTATAGGCATGC[A/T]CCATTATGCCCAGCT | 388795 |
rs1467795 | snp | A/G | 0.491263 | 0.0655142 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902818 | GTGAGGCTGGCTGCA[A/G]GGAAGCCAGACCCTC | 388795 |
rs1858621 | snp | A/G | 0.489492 | 0.0717183 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954718 | TTTTCTCTATTTCTA[A/G]TTAGCCAAGAGAGTT | 388795 |
rs1891776 | snp | A/G | 0.490231 | 0.0692021 | | | GRCh38.p7 | 20:32956284 | gaaagaaataataat[A/G]acaatgtcttatagg | 388795 |
rs1891777 | snp | A/T | 0.489837 | 0.0705577 | | | GRCh38.p7 | 20:32956089 | AAAACAACAATTTTT[A/T]AAATATTTGATTAAT | 388795 |
rs1891868 | snp | C/T | 0.369142 | 0.219784 | | | GRCh38.p7 | 20:32951302 | CCATCAATAGTTGAG[C/T]TGATAAACTATGGTT | 388795 |
rs1936201 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958326 | CAAGGGTCAGCTAGC[A/T]GCCCCTATCCTCAGC | 388795 |
rs1936202 | snp | A/T | 0.332106 | 0.236133 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957099 | atcaaatggacattc[A/T]aaaactaaaaaaata | 388795 |
rs1936307 | snp | G/T | 0.3742 | 0.216966 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941722 | AGTTGGGGAAATTGC[G/T]TAGTGACTACTGGGT | 388795 |
rs1936308 | snp | C/T | 0.36955 | 0.219562 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949931 | cttgaacctgggagg[C/T]ggaggctgcagtgag | 388795 |
rs1936309 | snp | C/G | 0.494143 | 0.0537956 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919956 | GCTGCTTTTCCCAGG[C/G]CAGTGTACCTACTGC | 388795 |
rs2000291 | snp | A/G | 0.381503 | 0.21262 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871729 | TGCGGGCTCCATACC[A/G]TGTCTTAGGCACCCC | 388795 |
rs2001639 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892959 | gattctcctgcctca[A/G]cctcctgagtagctg | 388795 |
rs2002257 | snp | C/T | 0.499891 | 0.00738737 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892982 | AGTAGCTGGGATTAC[C/T]GGTGCCCGCCACCAC | 388795 |
rs2014837 | snp | C/T | 0.403158 | 0.197592 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873276 | GAGCCCCCTGAACTC[C/T]GAGGATGTTGGCCAG | 388795 |
rs2017440 | snp | A/G | 0.039522 | 0.134904 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923314 | tattttagtagagac[A/G]gggtttcaccgtgtt | 388795 |
rs2019219 | snp | C/T | 0.469445 | 0.119766 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891277 | ACCAGAATTCAATAT[C/T]TTTTTTTCAACCAAA | 388795 |
rs2019230 | snp | A/G | 0.46865 | 0.121211 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891217 | GAGGCTGAGGCAGGA[A/G]AATCTCTTGAACCCG | 388795 |
rs2051119 | snp | A/G | 0.369754 | 0.219451 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956125 | CTCTGCTCTTTAAAT[A/G]GTATCTTTTGTATTA | 388795 |
rs2184150 | snp | A/C | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902649 | TCTGCATGCAGTGCA[A/C]TGTACAGGCCGGCAG | 388795 |
rs2377733 | snp | C/T | 0.444626 | 0.15691 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893132 | aggtgtgagccaccg[C/T]gcccagccCACACAA | 388795 |
rs2377734 | snp | C/T | 0.471846 | 0.115258 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893155 | CCACACAACCTCTTC[C/T]GTCTCCATCTTTCTG | 388795 |
rs2377735 | snp | C/T | 0.234109 | 0.249494 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934965 | caagggttttctttt[C/T]tctgcctcctcacca | 388795 |
rs4243972 | snp | C/T | 0.488905 | 0.0736498 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869487 | gtgatccgcctgcct[C/T]agcctcccaaagtgc | 388795 |
rs4264628 | snp | A/C | 0.021333 | 0.101051 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869424 | tatttttagtagaga[A/C]ggggtttctccatgt | 388795 |
rs4287835 | snp | C/T | 0.409382 | 0.192607 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869531 | gtgagctgctgtgcc[C/T]ggccaggtgttgcaa | 388795 |
rs4327299 | snp | A/G/T | 0.0185938 | 0.0946107 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872965 | AGTGTGATGGTGGGC[A/G/T]CCTGTAATCCCAGCT | 388795 |
rs4911269 | snp | A/T | 0.489608 | 0.0713316 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880186 | CAGGCCACGGGGAAG[A/T]CAAAGAGCTGGAAGG | 388795 |
rs4911270 | snp | A/G | 0.093777 | 0.195178 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881685 | gtgcctatctggatc[A/G]ttggtagcaaagcta | 388795 |
rs4911271 | snp | A/G | 0.499732 | 0.0115784 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885374 | GTTTATGGCGTGCGC[A/G]TGTGCGTGCGTGTGC | 388795 |
rs4911272 | snp | G/T | 0.498547 | 0.0269177 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885376 | TTATGGCGTGCGCAT[G/T]TGCGTGCGTGTGCGT | 388795 |
rs4911273 | snp | A/G | 0.375399 | 0.216275 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890647 | GAATTAGTACATGAA[A/G]TGACAGCTGGTGATG | 388795 |
rs5841120 | in-del | -/T | 0.389903 | 0.207189 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921201 | CTCTCCTTTTTTTTT[-/T]CTTGAGACAGGGTCT | 388795 |
rs6057660 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865580 | aggcaggaggatcac[C/T]tgaggtcaggagttc | 388795 |
rs6057661 | snp | C/T | 0.39214 | 0.205661 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870081 | CCTATTTACCTGCCC[C/T]GTGAATTTCTTTTGA | 388795 |
rs6057662 | snp | C/T | 0.388964 | 0.20782 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870159 | CAGTTTACGAACGAG[C/T]AAAGTGAGACCTAGG | 388795 |
rs6057663 | snp | G/T | 0.402982 | 0.197728 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875265 | TGTGAGGACAGAAGC[G/T]TCCGGAATTGGCCTA | 388795 |
rs6057664 | snp | A/C | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875414 | GGAGCCATCTCCCTT[A/C]TGTGCCCCCTGCAGT | 388795 |
rs6057665 | snp | A/G | 0.402982 | 0.197728 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875654 | GGATTGCAGGTACCC[A/G]CCACTGTGCCCAGCC | 388795 |
rs6057666 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877532 | TTCTCTTAATGTTCT[A/G]TAATAAACATTTCCT | 388795 |
rs6057667 | snp | A/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903382 | GCTTATGTCCCTTGC[A/G]GGACTCGCCATGATT | 388795 |
rs6057668 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904118 | tcctgcctcactttc[C/T]taagtagctgggact | 388795 |
rs6057669 | snp | A/G | 0.491157 | 0.065903 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904567 | gcctgccaaagtgct[A/G]ggattgcaggtgtga | 388795 |
rs6057670 | snp | C/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914191 | CCACAGGAGCCACAC[C/T]TAGAGTGGTCAAGGA | 388795 |
rs6057671 | snp | A/C | 0.49423 | 0.0534032 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914751 | atccactcacctcct[A/C]ccaggtccctccctc | 388795 |
rs6057673 | snp | A/G | 0.332106 | 0.236133 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932914 | CTAGTTCGTTTTAGT[A/G]TGAAGAGAATGTCAT | 388795 |
rs6057674 | snp | C/T | 0.488302 | 0.0755777 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933379 | TAGACATTTCTGAGG[C/T]ACAGTGTGCTGTTTT | 388795 |
rs6057675 | snp | A/G | 0.177182 | 0.23916 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935116 | gttggccatttgaat[A/G]tcttcttttgagaaa | 388795 |
rs6057676 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937229 | aggtgatccgactgc[C/T]tcggcctcccaaagt | 388795 |
rs6057677 | snp | A/C | 0.490231 | 0.0692021 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947459 | tctggtaacaaaaca[A/C]atctcactaatctca | 388795 |
rs6058912 | snp | C/T | 0 | 0 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859968 | ggtctcttgagtcac[C/T]tttcatctctaacag | 388795 |
rs6058913 | snp | C/T | 0 | 0 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860045 | cgcggtgactcacgc[C/T]tgtaatcccagcact | 388795 |
rs6058914 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861371 | tcggctcaccgcaac[C/T]tccgcctcctggatt | 388795 |
rs6058915 | snp | A/G | 0.453331 | 0.145452 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861384 | ACCTCCGCCTCCTGG[A/G]TTCAAGCAGTTCTCC | 388795 |
rs6058916 | snp | C/G | 0.45235 | 0.146814 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862858 | GGTCTCATTTGAACT[C/G]TTGACCTCAGGCAAT | 388795 |
rs6058917 | snp | A/T | 0.457388 | 0.139608 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863216 | GGATTGGTGCTCCAA[A/T]GACCCTAACAAAACG | 388795 |
rs6058919 | snp | A/G/T | 0.00716625 | 0.0594738 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866256 | TAGTTGGGGCTAAGT[A/G/T]GGGGAGAGTGAGCAA | 388795 |
rs6058920 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868015 | ctaattaaaattttt[C/T]ttttttttttagaaa | 388795 |
rs6058921 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870289 | GGACTCCATTGGTAC[C/T]GACCTTGGCCATCGT | 388795 |
rs6058922 | snp | G/T | 0.402465 | 0.201994 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870967 | aggttcaagtgattc[G/T]cctgtctcagcctcc | 388795 |
rs6058923 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875754 | cctcaagtgatccac[C/T]tgcctcagcctccca | 388795 |
rs6058924 | snp | A/G | 0.398534 | 0.201091 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876661 | GAATCCTATGGGGTA[A/G]GTGCTATTACTTACC | 388795 |
rs6058925 | snp | A/G | 0.398534 | 0.201091 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877568 | ACAATGAGGCCAACT[A/G]AAAGAAAAAGAATAA | 388795 |
rs6058926 | snp | C/T | 0.398534 | 0.201091 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877644 | CCCAGTGGTCCTTGT[C/T]TACAACCCCGTTTCT | 388795 |
rs6058927 | snp | A/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880882 | GGGCTGTGGGAGTTA[A/G]GAACTGTGGGCAAAA | 388795 |
rs6058930 | snp | A/G | 0.392696 | 0.205275 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881771 | gagttccaaactcgc[A/G]agccatttttaccat | 388795 |
rs6058931 | snp | C/T | 0.40263 | 0.198 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883206 | tgatatcacccaaga[C/T]atctgggtatttcag | 388795 |
rs6058932 | snp | A/G | 0.499946 | 0.00519141 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883251 | ttatatccttcagtc[A/G]taggggtagcttcag | 388795 |
rs6058934 | snp | C/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884601 | GTGGCTTGGGTTATC[C/T]TTAAGCCCAGGGTCA | 388795 |
rs6058935 | snp | A/C | 0.498632 | 0.0261223 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886641 | GTGGCTTCCATAGCC[A/C]TCCACCTTACCTTTC | 388795 |
rs6058936 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889085 | aggggttttaaagaa[A/G]gtgttctttaagccc | 388795 |
rs6058937 | snp | A/G | 0.499295 | 0.0187567 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889591 | GCTCGAATGAATACA[A/G]TGATGTTGAACAGAC | 388795 |
rs6058939 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890167 | GCCTTCAGAGGTCTG[A/G]GCCCTGCCGCCTCCA | 388795 |
rs6058940 | snp | A/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891344 | TTTGTTGGCTCATCA[A/G]GTGTctgggattaca | 388795 |
rs6058941 | snp | A/G | 0.497416 | 0.0358495 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891762 | CAGATGCGGGAGACA[A/G]CATGACGGTGAGGCT | 388795 |
rs6058942 | snp | A/G | 0.497416 | 0.0358495 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891922 | CAGTCTCAAACTCCT[A/G]GGCTCAAGCAGTCCT | 388795 |
rs6058943 | snp | C/T | 0.499793 | 0.0101816 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894295 | GGCCCCTGGCAGGCT[C/T]GTTGGGGCAGCGTCC | 388795 |
rs6058944 | snp | C/T | 0.487809 | 0.0771174 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894619 | GGACTTGGGAGGAGA[C/T]GGACAGACCCAGGTA | 388795 |
rs6058945 | snp | A/G | 0.490175 | 0.0693959 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895608 | gcagagtcttgctct[A/G]ttgcccaggctggag | 388795 |
rs6058946 | snp | G/T | 0.39527 | 0.203462 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895900 | aactcctggcctcaa[G/T]tgaccttcccacctg | 388795 |
rs6058947 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897557 | aggtgatcctcccac[C/T]tcaggcccccgagta | 388795 |
rs6058948 | snp | A/G | 0.498693 | 0.0255257 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898400 | CCGTGATCTCTGGGC[A/G]CCTCCAGTCCCAGCA | 388795 |
rs6058949 | snp | C/T | 0.413416 | 0.189196 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898753 | TAGTTTTTCCAGCAT[C/T]GCCAGCAGCAGCACG | 388795 |
rs6058950 | snp | C/G | 0.490673 | 0.0676508 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901908 | GGCCAGGATGGTCTT[C/G]ATCTCTTGACCTCAT | 388795 |
rs6058952 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910365 | GAGGCCCAGGCAGCA[A/G]GCAGCACCTTGGTCC | 388795 |
rs6058953 | snp | A/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910421 | GGCAGCTGGGCATGA[A/G]GAGTTGCTTCTGAGG | 388795 |
rs6058954 | snp | A/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914115 | GTCCTTTGAAATCTA[A/G]GTGGTGGAGGCAGCC | 388795 |
rs6058955 | snp | C/G | 0.491157 | 0.065903 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914553 | aattgactcacagtt[C/G]tgcatggctaggagg | 388795 |
rs6058956 | snp | A/T | 0.498503 | 0.0273153 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915076 | ctaattaaaaaaaaa[A/T]tttttttatagagat | 388795 |
rs6058959 | snp | C/T | 0.424348 | 0.179172 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925779 | TAGCTTGCCATGGCT[C/T]CTTCTGAAGGGACCC | 388795 |
rs6058960 | snp | A/G | 9.09711e-05 | 0.00674368 | missense | EFCAB8 | GRCh38.p7 | 20:32930476 | GACGGCTACATCTAC[A/G]CCTGGTCCCTCCATG | 388795 |
rs6058961 | snp | A/G | 0.342518 | 0.232251 | missense | EFCAB8 | GRCh38.p7 | 20:32930492 | CCTGGTCCCTCCATG[A/G]GAATGGAGGCCTGCT | 388795 |
rs6058962 | snp | C/T | 0.487809 | 0.0771174 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933057 | GGGATGGTGATAGTA[C/T]ATTATATATGCATTC | 388795 |
rs6058964 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937211 | tctcgaactccagac[C/T]tcaggtgatccgact | 388795 |
rs6058965 | snp | C/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938305 | tagaaatagaaactc[C/T]ttcaacctgataaaa | 388795 |
rs6058966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938312 | agaaactccttcaac[C/T]tgataaaagccattt | 388795 |
rs6058968 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940243 | gtaaatcaatggaat[A/G]gaatttagagttaaa | 388795 |
rs6058969 | snp | C/T | 0.249603 | 0.25 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942028 | AAGGCCTTTAATGTA[C/T]ACTACAAAATTGCAC | 388795 |
rs6058970 | snp | A/G | 0.235564 | 0.249583 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946844 | gatctgtttgtctct[A/G]tagttttgccttttc | 388795 |
rs6058971 | snp | C/T | 0.369142 | 0.219784 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953027 | aactttctgtttcta[C/T]gaatttaactacttt | 388795 |
rs6058972 | snp | C/T | 0.488666 | 0.0744214 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955358 | CAGCATGGGCAACAA[C/T]GTGAGACCCTGTCTC | 388795 |
rs6058973 | snp | A/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959533 | CCAGATCGGGTGTCA[A/G]GTCTGCATGGTGGAG | 388795 |
rs6087426 | snp | C/T | 0 | 0 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859743 | catgcccttttaccc[C/T]taaatacttttcagt | 388795 |
rs6087427 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872337 | CACAGAGAACAATGC[C/T]TGGCATGAAGTGCCA | 388795 |
rs6087428 | snp | A/C/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886900 | AGTTCCACTCAAGAG[A/C/T]TATGTGATCTTGGGT | 388795 |
rs6087429 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889998 | agagagagactcagt[C/T]ttaaaaaaaaaaaaa | 388795 |
rs6087430 | snp | A/C | 0.491783 | 0.0635686 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898034 | TGTGGTTCAAGTTGC[A/C]GTGAAATGCACATTC | 388795 |
rs6087431 | snp | C/T | 0.4941 | 0.0539917 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900517 | AGGCACGTGCCCCCG[C/T]GCTCAGCTAATTTTT | 388795 |
rs6087432 | snp | A/G | 0.117537 | 0.212022 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950918 | gaacttaaagtggca[A/G]tgtttgtccgagatg | 388795 |
rs6088027 | snp | G/T | 0 | 0 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860732 | TTTTCTGCATCTTGG[G/T]ttttttatttattta | 388795 |
rs6088028 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862354 | gctggtctcaaactc[A/C]tggatgcaagcgatc | 388795 |
rs6088029 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887475 | cagctacttgggagg[A/C]tgaggcacgagaatc | 388795 |
rs6088031 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890591 | atggatGATGAATGA[A/G]GCCTCTGACTGAGCA | 388795 |
rs6088032 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890666 | CAGCTGGTGATGTGA[A/G]GCTGAATGGGAGGAG | 388795 |
rs6088033 | snp | C/T | 0.498813 | 0.0243321 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898245 | CCCCATCCTCTAACT[C/T]ACAAGATTTCAAATG | 388795 |
rs6088034 | snp | A/G | 0.499839 | 0.00898417 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909094 | AGAGATGCGGGGGCC[A/G]CTCGTGCTTGAGCTC | 388795 |
rs6088035 | snp | C/T | 0.199564 | 0.24486 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909125 | CACCAAGGCCTCCCA[C/T]GCTCCGTGGGCTGGG | 388795 |
rs6088037 | snp | C/T | 0.389715 | 0.207315 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915637 | caatgcaagcttttt[C/T]tagcatggaccatcc | 388795 |
rs6088038 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915676 | cctattacctacttt[C/T]tttttttttttttaa | 388795 |
rs6088039 | snp | A/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915736 | gagtgcagtggtgca[A/G]tcttggctcactgca | 388795 |
rs6088040 | snp | A/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922241 | agtttttagctttta[A/G]gagcagcactgcatt | 388795 |
rs6088041 | snp | C/T | 0.039522 | 0.134904 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926907 | tcttaatccagtcta[C/T]cattgttggacattt | 388795 |
rs6088042 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929472 | cttccctcccctccc[C/T]tcccctcccctccgc | 388795 |
rs6088044 | snp | A/T | 0.48995 | 0.0701706 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947764 | aaaaaagttcaaatc[A/T]ccagcctcaacttcc | 388795 |
rs6088045 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949954 | gcagtgagccaagat[C/T]gcaccactgcactgc | 388795 |
rs6088046 | snp | A/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952335 | ttttgcctaacccaa[A/G]gtcacaaatgtttcc | 388795 |
rs6088047 | snp | G/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954660 | TTGGCTTTTAATTTA[G/T]CTCTATGATCCATCT | 388795 |
rs6088048 | snp | C/T | 0 | 0 | downstream-variant-500B | EFCAB8 | GRCh38.p7 | 20:32962301 | CATATCACCTGCAGC[C/T]TGAAGGGAGCTGGGG | 388795 |
rs6119295 | snp | C/T | 0 | 0 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860716 | ATCATAGTGTGCACC[C/T]TTTTCTGCATCTTGG | 388795 |
rs6119296 | snp | C/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861036 | gccactgtgcctggc[C/T]TGCATCGTGCTTTTC | 388795 |
rs6119297 | snp | A/G | 0.067446 | 0.170804 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871226 | ATGCAGTGGCAGCCT[A/G]TTGTCCACACTGTTC | 388795 |
rs6119298 | snp | C/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877211 | TTTAtttctttcttt[C/T]ttttttttttttttt | 388795 |
rs6119299 | snp | C/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880963 | AGAGAACACAGCTCC[C/T]TTATAGCAAAAGAAT | 388795 |
rs6119300 | snp | C/G | 0.465789 | 0.126365 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885677 | GGTGCACACATGGGT[C/G]ATTGGAGAGCCTCTG | 388795 |
rs6119301 | snp | C/G | 0.45843 | 0.138046 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886773 | GCTCTCTGGGAAGGC[C/G]CAGCAGGCCTGGATT | 388795 |
rs6119302 | snp | A/C | 0.4983 | 0.0291038 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910354 | AGGAAGGGACGGAGG[A/C]CCAGGCAGCAGGCAG | 388795 |
rs6119303 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910826 | cactgcagtctctgc[C/T]ttccgggttcaagcg | 388795 |
rs6119304 | snp | A/C | 0.34989 | 0.229177 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914526 | tggataatttatgac[A/C]aaaaagggtttaatt | 388795 |
rs6119305 | snp | C/T | 0.16911 | 0.236552 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921267 | GGTGTGATCACAGCT[C/T]ATTACAGCCTCAACT | 388795 |
rs6119306 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924136 | acagctcattgtagc[C/T]tccacttcccaggct | 388795 |
rs6119307 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924168 | aagcgattctcccac[C/T]tcagccttctgagta | 388795 |
rs6119308 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924261 | tagagatggagtctc[C/T]ttatgttgcccaggc | 388795 |
rs6119309 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933761 | aggcgggcagatcac[C/T]tgaggtcaggagttc | 388795 |
rs6119310 | snp | A/G | 0.24932 | 0.249999 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951138 | TTGGAAAGCATTTTG[A/G]CAGTTTCTTAAAAAG | 388795 |
rs6119311 | snp | C/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960036 | CCCCCAACTCGCAGC[C/T]TTCATTCTTGGGCGT | 388795 |
rs6120002 | snp | A/G | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860625 | gattctcgtgcctca[A/G]tctcccgagtagctg | 388795 |
rs6120003 | snp | C/T | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860989 | aagcgatcttcccac[C/T]ttggcctcaagtgtt | 388795 |
rs6120004 | snp | C/T | | | utr-variant-5-prime | EFCAB8 | GRCh38.p7 | 20:32860995 | tcttcccaccttggc[C/T]tcaagtgttggcatt | 388795 |
rs6120005 | snp | A/G | 0.336017 | 0.234736 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861043 | TGCCTGGCCTGCATC[A/G]TGCTTTTCTTATTAG | 388795 |
rs6120007 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874015 | aacctccgcctctca[A/G]gctcaagcaatcctc | 388795 |
rs6120008 | snp | A/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874198 | agtactgggattata[A/G]gtgtgaacACTTGCT | 388795 |
rs6120009 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875373 | GGGCTGGAGGAGGCA[A/G]CCTCCTAAGGGCCCC | 388795 |
rs6120010 | snp | C/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877000 | aaacaaaaaaCttac[C/T]tccatttgacagatt | 388795 |
rs6120012 | snp | C/G | 0.327914 | 0.237549 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884058 | TCTATTTCTTTGGGC[C/G]ATTTAGATCTCAAGG | 388795 |
rs6120013 | snp | A/C | 0.499218 | 0.0197529 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885852 | CTGGATGTCCATTCC[A/C]TGTGGGTGTCTCACA | 388795 |
rs6120015 | snp | C/T | 0.498346 | 0.0287064 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888858 | TAATAGCAGCTGCAG[C/T]GTCCCCTTTGAGTAG | 388795 |
rs6120016 | snp | A/G | 0.266 | 0.249487 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894213 | GCCCCATGCAGGGCC[A/G]CCAACCCCCTCTTCC | 388795 |
rs6120017 | snp | A/G | 0.392511 | 0.205404 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894489 | TGGTCTTTGAGCCAC[A/G]TGGTGAATGGGATAT | 388795 |
rs6120019 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895148 | CATGTTTGTCCCTGA[C/T]GGTGCTGGCTCTACT | 388795 |
rs6120020 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896303 | CCGCTCAGCTCACCA[A/G]GACACAGTGAGGTGC | 388795 |
rs6120021 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896659 | TGGTCTCTGGAAACA[A/G]GTTGCGGCAGCTGTT | 388795 |
rs6120022 | snp | A/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896940 | ttaccatggccgtca[A/G]gacgtgaggtgatct | 388795 |
rs6120024 | snp | C/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897412 | CGCACTCAGGGCGGT[C/T]TGGGTGATCCAACAG | 388795 |
rs6120025 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897543 | gacctcccgggctta[A/G]gtgatcctcccacct | 388795 |
rs6120026 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897561 | gatcctcccacctca[A/G]gcccccgagtagctg | 388795 |
rs6120027 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897759 | TTGGTTTTCCCTCCA[A/G]GTCTCACTCAGTGTC | 388795 |
rs6120028 | snp | A/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898970 | tgaagggttgcatga[A/G]gGAATCCTCTGTGGT | 388795 |
rs6120029 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899228 | gtctctactaaaaat[A/C]caataataataataa | 388795 |
rs6120030 | snp | C/T | 0.332106 | 0.236133 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900590 | TTTGTTTTTTTGTGA[C/T]GGAGTCTCACTGTGT | 388795 |
rs6120031 | snp | C/G | 0.387642 | 0.208697 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900848 | ACTGGGATTACAGGC[C/G]TGAGCCACCATGCCC | 388795 |
rs6120032 | snp | A/G | 0.490618 | 0.0678448 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904713 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTCCAGG | 388795 |
rs6120033 | snp | A/G | 0.458701 | 0.137636 | missense | EFCAB8 | GRCh38.p7 | 20:32906576 | GGTTGTCAGTGCTGC[A/G]TTTAAGGAAAGGGAT | 388795 |
rs6120034 | snp | A/C | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909577 | GAAAGGGACCTTGGA[A/C]TTGGAATTTGGGGTT | 388795 |
rs6120035 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910852 | aagcgattctcctgc[C/T]tcagcctcccgagta | 388795 |
rs6120036 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910969 | tctcaaacttctgac[C/T]tcaagtgatccaccc | 388795 |
rs6120037 | snp | C/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911037 | gccactgtgcccagc[C/T]TTACCTGCTACTCTT | 388795 |
rs6120038 | snp | A/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919473 | GGAAATGGGTGCATA[A/G]GTATATTTGCCCCTC | 388795 |
rs6120039 | snp | G/T | 0.48 | 0.0979796 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921393 | TGTGTGTGTGTGTGT[G/T]TTTGTAGAGATGGGG | 388795 |
rs6120040 | snp | G/T | 0.496483 | 0.0417852 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921431 | ATGCTGCCCATGCTG[G/T]TCTCGAACTCCTGGG | 388795 |
rs6120041 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927489 | agctgggattaaagg[C/T]gcccgccaccatgcc | 388795 |
rs6120042 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929716 | GTAAAGTTCTGAGCA[A/G]GAGTGAGGAAGCTTC | 388795 |
rs6120043 | snp | A/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929870 | CCCACATGGGCCACA[A/G]GTGTGACATGTAAGG | 388795 |
rs6120044 | snp | A/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929884 | AGGTGTGACATGTAA[A/G]GGAAAAGTGAGCAGA | 388795 |
rs6120045 | snp | G/T | 0.258565 | 0.249853 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930951 | CATGAGGCAGGGGTG[G/T]GCTGTCCTTGAGCCG | 388795 |
rs6120048 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935192 | TTTCTTTCTTTCttt[C/T]ttttttttttttttt | 388795 |
rs6120050 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937190 | tctccatgttggtca[A/G]gctggtctcgaactc | 388795 |
rs6120051 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937215 | gaactccagacctca[A/G]gtgatccgactgcct | 388795 |
rs6120052 | snp | A/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947918 | taaaaaaaaaaaaaa[A/G]gaaaaaagaaactag | 388795 |
rs6120053 | snp | C/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947919 | tctagtttctttttt[C/T]ttttttttttttttt | 388795 |
rs6120054 | snp | C/T | 0.332106 | 0.236133 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948437 | ctacagaaactcttc[C/T]agaaagttgaaaagg | 388795 |
rs6141352 | snp | C/T | 0.0148967 | 0.0850086 | missense | EFCAB8 | GRCh38.p7 | 20:32867688 | GGTCCCAGCTGTTTA[C/T]TGAGATACACCTGGC | 388795 |
rs6141353 | snp | G/T | 0.488118 | 0.0761554 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883507 | ttcatatagcttgaa[G/T]ggcgatttacatacc | 388795 |
rs6141354 | snp | C/T | 0.496746 | 0.040204 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884626 | GGGTCAGACCAGGCC[C/T]ACCGGATTTGGAAAG | 388795 |
rs6141355 | snp | C/G | 0.498589 | 0.02652 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886860 | TCATGCAGATGGAGA[C/G]ACCTCAAGTTTGAGG | 388795 |
rs6141832 | snp | A/G | 0.186421 | 0.24178 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860842 | CTTCTGGATGCAGGT[A/G]ATCCTCCCATCTCAC | 388795 |
rs6141833 | snp | A/T | 0.433818 | 0.169443 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863544 | CTTCTGCAGGACAAC[A/T]CCTCTCTATCAGGGG | 388795 |
rs6141834 | snp | A/C | 0.434109 | 0.169127 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863545 | TTCTGCAGGACAACT[A/C]CTCTCTATCAGGGGA | 388795 |
rs6141835 | snp | C/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876335 | GTGGTGCCCACCAAC[C/T]TCCCATTTGGCTTGG | 388795 |
rs6141836 | snp | A/G | 0.410061 | 0.192043 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878126 | CAAAAATTAGCTGGG[A/G]ATTGTGGCATGCATT | 388795 |
rs6141837 | snp | A/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879474 | cctctacccatctga[A/G]gttcattggcaggga | 388795 |
rs6141838 | snp | A/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881840 | gccagatgggatgaa[A/G]gcgcaatccaccccc | 388795 |
rs6141839 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881860 | aatccacccccatca[A/G]gcccttagggaattc | 388795 |
rs6141840 | snp | A/G | 0.398174 | 0.201356 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882607 | gtcactgcaacctcc[A/G]cttcctgggttcaag | 388795 |
rs6141841 | snp | C/T | 0.238749 | 0.249747 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883751 | GCTGGAGTGCAGTGG[C/T]GCAATCTTGGCTCAG | 388795 |
rs6141842 | snp | A/G | 0.498369 | 0.0285077 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886964 | TCTCTGAATAGTGCA[A/G]GGGTTGGGAGTTACC | 388795 |
rs6141843 | snp | A/G | 0.498611 | 0.0263212 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887065 | ATTGTCTTCACCGCC[A/G]GAACCACCTGGGGAG | 388795 |
rs6141844 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888238 | ccagctaattttttc[C/T]tttttgagatggagt | 388795 |
rs6141845 | snp | A/G | 0.499999 | 0.000798721 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889752 | CACTCCTGTAATACC[A/G]GCACTTCAGGAGGCC | 388795 |
rs6141846 | snp | C/T | 0.26271 | 0.249677 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895106 | AGCATTTGTGACCGC[C/T]TCCTTAAACTGCTCT | 388795 |
rs6141847 | snp | C/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905936 | ttggggtagcatgtc[C/T]taaaccccaTAACCC | 388795 |
rs6141849 | snp | C/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914112 | CCTGTCCTTTGAAAT[C/T]TAGGTGGTGGAGGCA | 388795 |
rs6141850 | snp | A/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914121 | TGAAATCTAGGTGGT[A/G]GAGGCAGCCATGTCC | 388795 |
rs6141851 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933948 | cgccactgcacttca[G/T]cctgggcaacaaagt | 388795 |
rs6141852 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937972 | gttctctatgaggcc[A/G]gtattaccttgatac | 388795 |
rs6141853 | snp | A/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950408 | aagagacttcactgt[A/G]agaattaaagaggaa | 388795 |
rs6141854 | snp | G/T | 0.0139853 | 0.0824443 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952397 | tcactcttacttttt[G/T]gtctataatcatttt | 388795 |
rs6141855 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958186 | TTCACATGTGGGGCA[A/G]GATGCTTTAGGCCTG | 388795 |
rs6141856 | snp | A/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958196 | GGGCAGGATGCTTTA[A/G]GCCTGAGCTCCGAGT | 388795 |
rs6579042 | snp | A/G | 0.392696 | 0.205275 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881069 | tatgaatgtctccca[A/G]gctgaggccattcag | 388795 |
rs6579050 | snp | A/G | 0.369754 | 0.219451 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952715 | ttttatcagtgtatc[A/G]cttgcccgttcattt | 388795 |
rs7262808 | snp | A/G | 0.120674 | 0.21395 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959312 | agtaaggaaggcttc[A/G]taggagaggtgattt | 388795 |
rs7263330 | snp | A/G | 0.119978 | 0.213528 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946895 | catacacatgtagct[A/G]agtgaaagtctaact | 388795 |
rs7266442 | snp | C/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885965 | CAGTGAATGGCATTG[C/T]CATCCCCAAGACTCC | 388795 |
rs7271178 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946766 | tagacattaccccaa[A/C]aagtgacctcatgtc | 388795 |
rs7271442 | snp | A/G | 0.375 | 0.216506 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947175 | gaaactttatgaaaa[A/G]tgaccaaactgtttt | 388795 |
rs7275157 | snp | C/T | 0.120326 | 0.21374 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944847 | aatataggtttcttt[C/T]cctttttaagatttg | 388795 |
rs7362756 | snp | C/G | 0.308661 | 0.24302 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904636 | ttttaaggcggtggc[C/G]gggtgggggtactga | 388795 |
rs7508877 | snp | C/T | 0.393434 | 0.20476 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939126 | ttctctctttctttc[C/T]ctttctttctttctt | 388795 |
rs7508972 | snp | C/G | 0 | 0 | missense | EFCAB8 | GRCh38.p7 | 20:32959797 | CAGCGGGATCTGGCT[C/G]AGGCCCTGATATACC | 388795 |
rs8115664 | snp | A/G | 0.488606 | 0.0746142 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949721 | aattcaaaatgggcc[A/G]tgcatgatggttcac | 388795 |
rs8119075 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878389 | caaacagagaAAGAG[C/T]AGGTCTGTTGCTTGG | 388795 |
rs8119838 | snp | A/G | 0.0741063 | 0.177655 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861319 | ttgagacggagttgc[A/G]ttcttgttgcccagg | 388795 |
rs8121390 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874379 | aggctcacgccacta[C/T]acctggctaatttaa | 388795 |
rs8123073 | snp | A/G | 0.0674403 | 0.170816 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859052 | TCCAAAAGATTGGAT[A/G]CCTCTGCTGAAGACC | 388795 |
rs8183625 | snp | C/T | 0.309648 | 0.24278 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896174 | GTTTAGATTGCAGCA[C/T]CTAGGAAGCGTGAGG | 388795 |
rs8184019 | snp | C/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861751 | agaTCGCCATGAACC[C/T]ttttttaattaaaat | 388795 |
rs8184203 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880388 | attctcccgcctcag[C/G]gtcccaagtagctgg | 388795 |
rs9967910 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883407 | gggctatccagtgga[C/G]aatttgtccctgcca | 388795 |
rs9967934 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883516 | cttgaatggcgattt[A/G]catacctctgtttta | 388795 |
rs10211797 | snp | A/G | 0.0759472 | 0.179459 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886378 | ACTGTGTACTTGGTC[A/G]CCAGGGCCGTCCAGA | 388795 |
rs10693739 | in-del | -/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897456 | TTTTTTTTTTTTTTT[-/T]GGTTGAGTCAGGGCC | 388795 |
rs10706429 | in-del | -/C | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955015 | CTGGACATCTATCCT[-/C]CCCATGAGTAGAGTG | 388795 |
rs11167181 | in-del | -/C | 0.460365 | 0.13508 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865320 | TGTGTATGGGAGACA[-/C]ACGTGAGTAAGCACC | 388795 |
rs11167182 | snp | A/G | 0.381891 | 0.212379 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867964 | GTCTCAGCCCCCAGA[A/G]TAGCTGGGACTACAT | 388795 |
rs11167183 | snp | C/G | 0.383053 | 0.211653 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876295 | CTACTGAGTGTGCAG[C/G]GGTGACCCCACCTGC | 388795 |
rs11167184 | in-del | -/ACCTCCATG | 0.499663 | 0.0129749 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890494 | CTCCTCCAGACTGGA[-/ACCTCCATG]AAGGTCAGGGACTGC | 388795 |
rs11167185 | snp | A/G | 0.301681 | 0.2446 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894328 | TGCTGGCAGAGCAGG[A/G]ACAGATCCTGTCCTG | 388795 |
rs11167186 | snp | A/T | 0.302435 | 0.244439 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896611 | TGCAAAAAGTGGATT[A/T]ACTCCCTGGGTTCAG | 388795 |
rs11167187 | snp | C/T | 0.127599 | 0.217986 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934771 | TGCTCCCATGTAAGA[C/T]GTGCCTTTGCTCCTC | 388795 |
rs11167188 | snp | A/G | 0.370162 | 0.219229 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960724 | CCTGTGGTCCCCTTA[A/G]GAATAAATGAGATAA | 388795 |
rs11167189 | snp | A/G | 0.387642 | 0.208697 | utr-variant-3-prime | EFCAB8 | GRCh38.p7 | 20:32961618 | GTTCTGAGGTGCTCC[A/G]CTGTCTTCTCTAGTC | 388795 |
rs11167190 | snp | G/T | 0.46855 | 0.121392 | utr-variant-3-prime | EFCAB8 | GRCh38.p7 | 20:32961778 | ATCTTGTCTTCTCTC[G/T]GGCCCCGCACAGAGC | 388795 |
rs11353110 | in-del | -/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895314 | TTTTTTTTTTTTTTT[-/T]ACATTTTGAGACAAG | 388795 |
rs11469615 | in-del | -/TT | 0.378174 | 0.214642 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861920 | TTAACAGAAATGAAC[-/TT]AACATTTTACATACA | 388795 |
rs11472143 | in-del | -/TT | 0.492775 | 0.059668 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921700 | TTTTAGCCTTGTACT[-/TT]TTTTTTTTTTTGACT | 388795 |
rs11473489 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888081 | TTTCTTTTTTTTTTT[-/T]GAGACTGGGTCTTGC | 388795 |
rs11474795 | in-del | -/CCTCCATGA | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890495 | TCCTCCAGACTGGAA[-/CCTCCATGA]GGTCAGGGACTGCAT | 388795 |
rs11478583 | in-del | -/T | 0.494568 | 0.0518327 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863012 | ACTTTTTGCTGCCAA[-/T]TTTTTTTTTTTTCCT | 388795 |
rs11483441 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921848 | TTGTTACCTTATTCT[-/T]TTTTTTTTTTTTTTT | 388795 |
rs11483446 | in-del | -/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929511 | TTTTTTTTTTTTTTT[-/T]CTTTAAATAGAGATA | 388795 |
rs11483513 | in-del | -/A | 0.494774 | 0.0508504 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932376 | TCTCAAAAAAAAAAA[-/A]TTATTCAGTACTACA | 388795 |
rs11483888 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917006 | CAATGTCCCCCCCCC[-/C]TTTAAACCTTAATCC | 388795 |
rs11696131 | snp | C/T | 0.295599 | 0.245806 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899735 | ACGCACCACCATGCT[C/T]GGCTAATTTTGTATT | 388795 |
rs11696188 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921416 | AGATGGGGTCTCACT[A/G]TGCTGCCCATGCTGG | 388795 |
rs11696588 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935922 | atattttctgtcact[C/T]tgtgggttatctctt | 388795 |
rs11696923 | snp | A/G | 0.0984431 | 0.198823 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919087 | ACAGTTCTATTTTGC[A/G]GGGAGTAGGGAGAAA | 388795 |
rs11696936 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933611 | accaataacttccca[A/T]tctctctcccttatt | 388795 |
rs11697030 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926874 | catagtattccatgg[G/T]gtatatgtgccacat | 388795 |
rs11697050 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926949 | aagtctttgctattg[G/T]gaataatgccgcaat | 388795 |
rs11697249 | snp | A/G | 0.030665 | 0.119967 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898052 | GAAATGCACATTCTC[A/G]TGCCCTCCGCGCTTC | 388795 |
rs11697394 | snp | A/G | 0.398534 | 0.201091 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872270 | TGGGCAAGCAACCAC[A/G]CCTCTCTGTGCCACA | 388795 |
rs11697410 | snp | A/T | 0.0387552 | 0.1337 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923029 | tctctacaaaaaatt[A/T]aaaaaattagccagg | 388795 |
rs11697690 | snp | C/T | 0.424503 | 0.179021 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890175 | AGGTCTGAGCCCTGC[C/T]GCCTCCAGTAGTCTC | 388795 |
rs11697892 | snp | A/G | 0.310632 | 0.242536 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872781 | CCTGGGCAACAGAGC[A/G]AGACTCCATCTCAAA | 388795 |
rs11697940 | snp | G/T | 0.317692 | 0.240661 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886196 | TCTGTCAAATGGGGC[G/T]AGTTACAGTGCTTCT | 388795 |
rs11697967 | snp | A/C | 0.387832 | 0.208572 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923896 | TGAATACCCTTGTAC[A/C]TAAATTTTGGATCTC | 388795 |
rs11697992 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895485 | acgccaccaccactt[C/G]tggctaattttttat | 388795 |
rs11698654 | snp | A/G | 0.108048 | 0.20579 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861491 | ATGGGATTTCTCCAT[A/G]CTGGCCAGGCTGGTC | 388795 |
rs11698786 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922310 | GTATATTGAGAGGAC[A/G]GATTCTTGGAAACAG | 388795 |
rs11698849 | snp | C/T | 0.108402 | 0.206034 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861702 | CCAGGAGTGCAAAAC[C/T]AGCCTGGGCAACATT | 388795 |
rs11699245 | snp | A/C | 0.0240643 | 0.107019 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919091 | TTCTATTTTGCGGGG[A/C]GTAGGGAGAAAGAGC | 388795 |
rs11699338 | snp | C/T | 0.499961 | 0.0043928 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922444 | TCGCTACATGCCAGC[C/T]GCTGGGGAAGGAGCA | 388795 |
rs11699811 | snp | C/T | 0.121717 | 0.214577 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956530 | atatctttattttgc[C/T]gtaaaatttaagact | 388795 |
rs11699965 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893767 | CTGGGCATGGCCTGG[C/T]TGGCATGGGTGAGTG | 388795 |
rs11700000 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931972 | AAATGATTGTTTTTG[C/T]TGGGGGAGTGGAGAG | 388795 |
rs11700082 | snp | A/G | 0.398894 | 0.200825 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872438 | TGGGGCAACAGGCTC[A/G]TGCCTGCCATCCCAG | 388795 |
rs11700194 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895847 | aagtgctgggattac[A/C]ggcgtgagccaccgt | 388795 |
rs11904943 | snp | C/T | 0.0759472 | 0.179459 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915307 | cttcaatatgttaca[C/T]agaaatttgctcagt | 388795 |
rs11906931 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926960 | attgtgaataatgcc[A/G]caataaacatacgtg | 388795 |
rs11908197 | snp | A/T | 0.0744748 | 0.178019 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944471 | ctctgtctaaaaaaa[A/T]aataataataaaaat | 388795 |
rs12329625 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901958 | cccaaagtgctggga[C/T]tacaggcgtgagcca | 388795 |
rs12480123 | snp | C/T | 0.487368 | 0.0784625 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879569 | TGACACGGGAGCCTC[C/T]GTAGGAAATGAAGCC | 388795 |
rs12480689 | snp | C/G | 0.309894 | 0.242719 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903495 | CGTGTCTGTGCCCCT[C/G]GTAATCCTGGCAGGA | 388795 |
rs12624525 | snp | C/T | 0.232359 | 0.249377 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890658 | TGAAATGACAGCTGG[C/T]GATGTGAGGCTGAAT | 388795 |
rs12624751 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954051 | cctcaggtgatacac[A/C]tgcctcagcctccca | 388795 |
rs12624878 | snp | C/G | 0.0792508 | 0.182605 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902328 | CTGTGTTGTGGGATG[C/G]AGGGACTGGAGATGT | 388795 |
rs12625029 | snp | G/T | 0.0425829 | 0.139564 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907904 | TGTGGCAACTATGTT[G/T]GTAGCCACTACCGGA | 388795 |
rs12625153 | snp | C/T | 0.398534 | 0.201091 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872912 | gcctggccaacatgg[C/T]gaaaccctgtctcta | 388795 |
rs13036333 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891325 | CTGGTCTGCTGGGCC[C/T]GTGTTTGTTGGCTCA | 388795 |
rs13037174 | snp | C/T | 0.403158 | 0.197592 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878541 | tttgagacggagtct[C/T]gctctgtcgcccagg | 388795 |
rs13037187 | snp | C/T | 0.403158 | 0.197592 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878558 | ctctgtcgcccaggt[C/T]ggactgcggactgca | 388795 |
rs13037496 | snp | C/T | 0.446149 | 0.155002 | missense | EFCAB8 | GRCh38.p7 | 20:32878728 | GTGGATTACATGATG[C/T]GTGAGTTCCAGGGAA | 388795 |
rs13037762 | snp | A/G | 0.403158 | 0.197592 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878581 | GGACTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC | 388795 |
rs13037781 | snp | C/T | 0.47879 | 0.100772 | missense | EFCAB8 | GRCh38.p7 | 20:32917486 | CCTCTAGGAGCCCCT[C/T]GCCCTTGCAGCCCAA | 388795 |
rs13037833 | snp | C/T | 0.398714 | 0.200958 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871756 | CCCCAACTGTCACTG[C/T]GTGCCTTGGAGGGAA | 388795 |
rs13038017 | snp | C/T | 0.402806 | 0.197864 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879745 | GTGTCCCTGTGTCTT[C/T]GGGCACCCCTCACAT | 388795 |
rs13038409 | snp | G/T | 0.497829 | 0.0328757 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889724 | TAGCCTCTCCTGGCC[G/T]GGTGTGGTGGCTCAC | 388795 |
rs13038551 | snp | A/G | 0.498034 | 0.0312882 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889794 | ATCACCTGAGGTCAG[A/G]AGTTCAAGACCAGCC | 388795 |
rs13038628 | snp | C/T | 0.021333 | 0.101051 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880720 | aacagatgtgtaggg[C/T]gaggtatggggagag | 388795 |
rs13038717 | snp | A/G | 0.355954 | 0.226437 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882678 | ggtggccgccaccac[A/G]cctggccgatttttt | 388795 |
rs13038811 | snp | A/G | 0.377187 | 0.215229 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905614 | aaaatacaaaaatta[A/G]ccaggcgtggtggtg | 388795 |
rs13038881 | snp | C/T | 0.402806 | 0.197864 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880307 | AGAGTCTCACTCAGT[C/T]GCCCAGGTTGGAGTG | 388795 |
rs13039274 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888316 | ctgcagcctctgcct[C/G]ccgggttcaggtgat | 388795 |
rs13039718 | snp | C/T | 0.497359 | 0.0362457 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882596 | catcatctcaggtca[C/T]tgcaacctccacttc | 388795 |
rs13040407 | snp | A/C | 0.192715 | 0.243348 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946328 | ttcccaatctgcttc[A/C]ctgagccaggaggag | 388795 |
rs13040524 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928247 | gattttttatttttt[A/T]ttttttgagacagag | 388795 |
rs13041458 | snp | G/T | 0.403205 | 0.198165 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879570 | GACACGGGAGCCTCT[G/T]TAGGAAATGAAGCCC | 388795 |
rs13041716 | snp | C/G | 0.490287 | 0.0690083 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930746 | TGTGAAACAATGCAG[C/G]GAGGAGTCCTCTCCT | 388795 |
rs13042128 | snp | A/G | 0.00934559 | 0.067716 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887169 | TTCCCTATCCCTTCT[A/G]ATTATCCATCTAGAG | 388795 |
rs13042514 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878232 | gatcacaccattgca[C/G]tccagcctgggtgac | 388795 |
rs13042651 | snp | C/T | 0.402454 | 0.198136 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879617 | CTGAGGGTTTTCATG[C/T]TAGGTTCAATGGAGG | 388795 |
rs13043121 | snp | A/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946790 | tcatgtctcctcata[A/G]taaactctatttcct | 388795 |
rs13043425 | snp | C/T | 0.239942 | 0.249798 | missense | EFCAB8 | GRCh38.p7 | 20:32917383 | AGCATGGCCAAGTAC[C/T]GGAACCAGTTCCTTG | 388795 |
rs13043436 | snp | A/G | 0.310878 | 0.242475 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871317 | TTTCCTGTGTAGCCC[A/G]GGGTGGAGTGCAGTG | 388795 |
rs13043706 | snp | A/C | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940097 | TTGCTTTTtggagat[A/C]caagggatatagata | 388795 |
rs13044434 | snp | C/T | 0.021333 | 0.101051 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889727 | CCTCTCCTggccggg[C/T]gtggtggctcactcc | 388795 |
rs13044679 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891169 | ggctggagtgcagtg[A/G]cacaatctcggctca | 388795 |
rs13045180 | snp | C/T | 0.227074 | 0.248947 | stop-gained | EFCAB8 | GRCh38.p7 | 20:32943738 | TATGTGGACAACTTC[C/T]AGCTGGTTATCAGCG | 388795 |
rs13045548 | snp | C/T | 0.278133 | 0.248412 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928940 | ctgcatcaattaaga[C/T]gatcgtgtgggtttt | 388795 |
rs13339906 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946852 | tgtctctatagtttt[A/G]ccttttccagattat | 388795 |
rs13339907 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947041 | attcaccaattatag[A/G]acatttgagtcattg | 388795 |
rs13339911 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955291 | atgcctgtaatcaca[A/G]cactttgacagacca | 388795 |
rs13339913 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955412 | gggcatggaagtgtg[C/T]acctgtagtcccagt | 388795 |
rs17123726 | snp | A/G | 0.0345262 | 0.126772 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859562 | CTCCTGGTGAAAGAC[A/G]TTTATCTTACAAAAT | 388795 |
rs17123730 | snp | C/G | 0.029116 | 0.117091 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863437 | CTACCACATGGCCTC[C/G]TAAGATTCTTCTACT | 388795 |
rs17123731 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865119 | TGCCTTGCTGCCCAC[A/G]TGTATGGACAGACAA | 388795 |
rs17123741 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871915 | CAGGAGGTTTTGAAA[A/G]CACACAAAGGCAGTT | 388795 |
rs17123797 | snp | G/T | 0.0479149 | 0.147179 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885750 | TTCATGGTCTAAGCA[G/T]CCTGGACTTGCAGTC | 388795 |
rs17123810 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886524 | AGTTGCATCAGGGCT[C/T]ATCCTTTGGGGAAGA | 388795 |
rs17123850 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902124 | TTCTCTAAGTACCTC[A/G]GAGTATCTTCTTACA | 388795 |
rs17123854 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906202 | ATGCCTGTCCCAGTA[C/T]AGTTGATGTGAAAAT | 388795 |
rs17123864 | snp | C/T | 0.182296 | 0.240658 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917206 | TATCCTCCTCTGAGT[C/T]GGCTCCCAGAATCCT | 388795 |
rs17370071 | snp | C/T | 0.387453 | 0.208822 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865150 | GCACACTTACTATGC[C/T]TTGAGGGGCAGATAT | 388795 |
rs17370942 | snp | C/T | 0.296619 | 0.245615 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908171 | AAGTGCTTGGACGGA[C/T]GATGTGCCCTGGCCT | 388795 |
rs17371144 | snp | G/T | 0.15698 | 0.23205 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920346 | TGCCCGGAAGGCATC[G/T]TGGAGAGGATGGAGA | 388795 |
rs28450024 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901929 | TTGACCTCATGATTC[A/G]CCCGCCTCGGCCTCC | 388795 |
rs28450271 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882205 | ACTCCGTCTCAAAAA[A/G]AAAAAAAAAAACAGC | 388795 |
rs28464223 | snp | A/G | 0.255224 | 0.249945 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913479 | TGAATTTTGGGAGCA[A/G]AATTCAGTCTATGGC | 388795 |
rs28885496 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949995 | ACAGAGCAAGACTCT[A/G]TCTCAAAAACAAACA | 388795 |
rs34005846 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894723 | ATGGCCCTACTTCCC[-/C]TGATAGCTTTGGTAT | 388795 |
rs34034569 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863479 | TGTGATCCCCTTTAG[-/G]AAGCCTCTGGCATTA | 388795 |
rs34038793 | multinucleotide-polymorphism | CT/TG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879569 | TGACACGGGAGCCTC[CT/TG]TAGGAAATGAAGCCC | 388795 |
rs34039814 | snp | C/T | 0.021333 | 0.101051 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870710 | TCTTGCTATGTTGCC[C/T]AGGCTAGTCTCAAAC | 388795 |
rs34084944 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881740 | CCATTCTCATTCATA[A/G]AGAATAGGGTTACAC | 388795 |
rs34111982 | snp | A/G | 0.301932 | 0.244547 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891203 | CAACCTCTGCCTCCC[A/G]GGTTCAAGAGATTTT | 388795 |
rs34185318 | in-del | -/T/TT | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910759 | TTTTTTTTTTTTTTT[-/T/TT]TGCCAGGGTCTCGCT | 388795 |
rs34199943 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879129 | CCCAGTATACAGCAT[-/T]GCTTCACCTGCTTCC | 388795 |
rs34232014 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888895 | ACACACCCATAGAAA[C/T]GTCTTGGAAACAGAT | 388795 |
rs34282547 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907683 | ATTTTCCCAGAAGCC[-/C]TGGGAGCTGGGATCA | 388795 |
rs34301359 | in-del | -/C | | | utr-variant-3-prime | EFCAB8 | GRCh38.p7 | 20:32961795 | GCCCCGCACAGAGCC[-/C]TGGGGCAGAAAATAA | 388795 |
rs34308609 | in-del | -/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895335 | TTTTTTTTTTTTTTT[-/T]ACATTTTGAGACAAG | 388795 |
rs34371315 | in-del | -/C/CAAA/CAAT/CGAA | 0.434253 | 0.168969 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950012 | TCAAAAACAAACAAA[-/C/CAAA/CAAT/CGAA]ACAACAAAACAACAA | 388795 |
rs34379554 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914901 | TTCCATTTTTTTTTT[-/T]CTTTAAGACATGGGA | 388795 |
rs34385534 | in-del | -/C | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934287 | GACAGGATTTTTTTT[-/C]CTCTTTTAAGGCTGA | 388795 |
rs34398836 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871491 | GCTATGCTGTATTCC[-/C]TTGCTTTTTTAAAAA | 388795 |
rs34402429 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901848 | CGCGCCATCATGCCC[-/C]GGCTAATATTTGCAT | 388795 |
rs34406038 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951085 | GAGCTGAAACTCTCC[-/C]TGCACGGCTAATGGG | 388795 |
rs34439877 | in-del | -/AAT | 0.357816 | 0.225556 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899230 | AATAATAATAATAAT[-/AAT]TAGCCGGGCGTGGTG | 388795 |
rs34467684 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907672 | TCCTGTCTGGAATTT[-/T]CCCAGAAGCCCTGGG | 388795 |
rs34524376 | snp | A/G | 0.031825 | 0.122064 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891640 | AACAGTGTGATCCCC[A/G]GCCTTTGTGGCCCCA | 388795 |
rs34560157 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914916 | TTTTTTTTTTCTTTA[A/G]GACATGGGATCTCAC | 388795 |
rs34569597 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861579 | CAGATGTGAGCCACC[A/G]CGCCTAGCCGTTGAA | 388795 |
rs34585231 | in-del | -/G | | | frameshift-variant | EFCAB8 | GRCh38.p7 | 20:32961215 | TCCTGACCAGCAGGG[-/G]CCCAGACCAGCAAGA | 388795 |
rs34622972 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896304 | GCTCAGCTCACCAGG[-/C]ACACAGTGAGGTGCC | 388795 |
rs34645161 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914036 | CCTGTGGCACTTCCC[-/C]TGCATGAGCCCCCTG | 388795 |
rs34659645 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947462 | GTAACAAAACAAATC[-/C]TCACTAATCTCAAAA | 388795 |
rs34691205 | snp | C/T | 0.211516 | 0.24702 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928298 | TGGAGTACAATGGCA[C/T]GATCTCGGCTCACTG | 388795 |
rs34703125 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894091 | TACGGCTCAGGGCCG[C/T]CTAGGGAACTCATCT | 388795 |
rs34708348 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888193 | TCAGCCTCCCAAGTA[-/A]GCTGGGACTACAGGC | 388795 |
rs34729584 | in-del | -/C | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860631 | GTGCCTCAGTCTCCC[-/C]GAGTAGCTGGGATTA | 388795 |
rs34729861 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907036 | CTTCTGTTCCTCAGG[-/G]AAACACACTGGCCAG | 388795 |
rs34790004 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900077 | CCAGGAGAGTCTTTT[-/T]GGGGGAACAGCAGGA | 388795 |
rs34804298 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906224 | GTGAAAATCAAATTT[-/T]GCCCTTGGAATGAGG | 388795 |
rs34805035 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861726 | CAACATTGCAAGACC[C/G]CATCTCAAAAGATCG | 388795 |
rs34806638 | snp | C/T | 0.499477 | 0.0161657 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889949 | GAGGTTGCAGTAAGC[C/T]GAGATCGCGCCATTG | 388795 |
rs34866340 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923278 | TTGCCTGAGCTCAGG[-/G]AGTTCGAAACCAGCC | 388795 |
rs34867308 | snp | C/T | 0.180383 | 0.240111 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936192 | CGTGTGCCACCATGC[C/T]TAGCTAATTTTTGTA | 388795 |
rs34915357 | in-del | -/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915689 | TTTTTTTTTTTTTTT[-/T]AAGACAGAGTCTTGT | 388795 |
rs34962667 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862517 | ATCTCCTTCCCTTAG[-/G]CTGTCCTCTCTCCTT | 388795 |
rs34996370 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945147 | GCTCTAGAATTTCTG[G/T]TATTTTTATTATTAT | 388795 |
rs35059142 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950039 | ACAACAACAACAACA[-/A]AAATGGAACATAGAA | 388795 |
rs35076019 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865625 | AACATGGTGAAACCC[-/C]TGTCTCTACTAAAAA | 388795 |
rs35090283 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861128 | TTGGGTGACGTCCTA[A/G]GTGCAGATGCACTGA | 388795 |
rs35092353 | in-del | -/C | 0.021333 | 0.101051 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878408 | CTGTTGCTTGGCCAC[-/C]TGCCCTGGCCAGTAC | 388795 |
rs35100463 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904495 | TACAGATGGGATCTT[-/T]GCTGTGTTGCCCAGG | 388795 |
rs35124409 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870681 | TTTTTAAAAACTTTT[-/T]GGTAGAGATGGGGTC | 388795 |
rs35160768 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942692 | CCCATTGTGATATTT[-/C]TCCTTTGCCTGTTTA | 388795 |
rs35201561 | snp | C/G | 0.21695 | 0.247806 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928514 | TGCTGGGATTACAGG[C/G]ATGAGCCACCGCACC | 388795 |
rs35208902 | snp | C/T | 0.359152 | 0.224913 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926098 | CAGTCCTGCTGAAGT[C/T]CTGGGCGCTCATTCA | 388795 |
rs35227113 | in-del | -/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880279 | CTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCAC | 388795 |
rs35271121 | snp | C/T | 0.382666 | 0.211895 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880005 | TGGGCCTGGGCTGCC[C/T]GGGTCACTGGATCCC | 388795 |
rs35298078 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913016 | ATCTGCTCATCCATC[A/C]ATTTATTCATTATTC | 388795 |
rs35301817 | in-del | -/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895589 | CTTTTTTTTTTTTTT[-/T]AAGGCAGAGTCTTGC | 388795 |
rs35356622 | snp | A/G | 0.305186 | 0.243833 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928404 | CCACACCTGGCTAAT[A/G]TTTGTATTTTTTAGT | 388795 |
rs35358527 | snp | C/T | 0.332337 | 0.236052 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954054 | CAGGTGATACACCTG[C/T]CTCAGCCTCCCAAAG | 388795 |
rs35366149 | in-del | -/A | 0.261907 | 0.249716 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928246 | GATTTTTTATTTTTT[-/A]TTTTTTTGAGACAGA | 388795 |
rs35385905 | in-del | -/G | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859425 | AGGAATGGTACTTGT[-/G]CTTGGCCTCTCCCCT | 388795 |
rs35416693 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909602 | GGGGTTCTAGGAACA[-/C]TAGGGTTTGGAAGGC | 388795 |
rs35429537 | in-del | -/TA | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880908 | AAAACATATATATAT[-/TA]ATAAAACACCACAGG | 388795 |
rs35458916 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941471 | AAGTGGAAACAACCC[-/C]AAATGTCAACTTCCA | 388795 |
rs35459528 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943043 | TTTATTAATCTTGTT[-/C]TTATTTAAAAATGGT | 388795 |
rs35462744 | in-del | -/A | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865811 | AAAAAAAAAAAAAAA[-/A]TTTGCTGCCTAGAAA | 388795 |
rs35490306 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960710 | GAGCTCCCTCCTCCC[-/C]TGTGGTCCCCTTAAG | 388795 |
rs35499815 | snp | C/G | 0.392696 | 0.205275 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939242 | TTTCCCTCCCTCCCT[C/G]CCTTCCTTCCTTCCA | 388795 |
rs35511798 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946763 | CATAGACATTACCCC[-/C]AAAAAGTGACCTCAT | 388795 |
rs35519090 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881864 | CACCCCCATCAGGCC[-/C]TTAGGGAATTCTGAC | 388795 |
rs35529202 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920825 | CCCTCTGGATTGGGG[-/G]TAACAGTGTCCCCTC | 388795 |
rs35534837 | in-del | -/TT | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870872 | TTCTTTTTTTTTTTT[-/TT]CCTGAAATGGAGTCT | 388795 |
rs35546420 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956879 | TCTCTCCTCTCATTG[G/T]GGGGGTACTAACTAT | 388795 |
rs35572889 | snp | G/T | 0.129664 | 0.219133 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931673 | TGAGGCAGGAGAATC[G/T]CTTGAACCTAGAAGG | 388795 |
rs35614431 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953921 | TTCAAGCGATCCTCC[-/C]TGCCTCAGCCTCCCG | 388795 |
rs35668122 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947715 | ACAGTAGTAACGGGG[-/G]AAATTTGTAGCACTA | 388795 |
rs35670293 | in-del | -/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878528 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCGC | 388795 |
rs35672324 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932046 | CTCTGCTTCATTAAC[-/C]GGGCCTGATCATGCA | 388795 |
rs35684392 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886882 | GTTTGAGGCGGGGCC[-/C]TGAGTTCCACTCAAG | 388795 |
rs35722979 | snp | C/T | 0.391954 | 0.205789 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939518 | TCAAACTCCTGACTT[C/T]GTGGTCCGCCTGCCT | 388795 |
rs35725555 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890202 | CTCCACCTGTCCCCT[-/C]CCCTGTGGTGCTGAG | 388795 |
rs35737599 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876520 | GAATATACAGCTTTT[-/T]AAGCATACAGAAAAG | 388795 |
rs35759361 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911424 | GGCTGGAGACCACCC[-/C]TTGGGAGTGGAGGCC | 388795 |
rs35765948 | snp | C/T | 0.021333 | 0.101051 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871234 | GCAGCCTATTGTCCA[C/T]ACTGTTCTATTCTTT | 388795 |
rs35777748 | snp | C/T | 0.194278 | 0.243711 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911013 | AAAGTTTTAGGATTA[C/T]AGGCGTGAGCCACTG | 388795 |
rs35786578 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894386 | TGCCTCATTGGCCTC[A/G]GGTGCCTGCCCTGCC | 388795 |
rs35804348 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917053 | GTGTCTGACTGGGGG[-/G]TGTATTACACATTGA | 388795 |
rs35810642 | in-del | -/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904624 | TTTTTTTTTTTTTTT[-/T]AAGGCGGTGGCGGGG | 388795 |
rs35810671 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871320 | CCTGTGTAGCCCAGG[-/G]TGGAGTGCAGTGGTG | 388795 |
rs35814833 | in-del | -/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891842 | TTTTTTTTTTTTTTT[-/T]AATTGAGACAGGGTC | 388795 |
rs35881463 | in-del | -/C | 0.499663 | 0.0129749 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885139 | CTCTGCTCACCCTCT[-/C]CTGGGCAGTTTTTCC | 388795 |
rs35903617 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897620 | TTTTAATTCTTTTTT[-/T]GAGACGGGGCCTCAC | 388795 |
rs35904347 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948027 | TAAAAAATAATAAGG[-/G]AAAATCAATGAACCC | 388795 |
rs35919572 | snp | C/T | 0.148996 | 0.228688 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894078 | GATCCCCAGAGGATA[C/T]GGCTCAGGGCCGCCT | 388795 |
rs35940814 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904624 | TTTTTTTTTTTTTTT[-/T]AAGGCGGTGGCGGGG | 388795 |
rs35944660 | snp | A/G | 0.177503 | 0.239258 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929594 | TGATTCACCCGCCTC[A/G]GCCTCCCAAAGTGCT | 388795 |
rs35981850 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898745 | TGGGGTTTAGTTTTT[-/T]CCAGCATTGCCAGCA | 388795 |
rs35995511 | snp | A/C | 0.395818 | 0.203069 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873810 | GAGCGAGACTCTGTC[A/C]AAAAAAAAAAAAAAT | 388795 |
rs36000901 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891842 | GTTTTTTTTTTTTTT[-/T]AATTGAGACAGGGTC | 388795 |
rs36022156 | snp | C/T | 0.039522 | 0.134904 | missense | EFCAB8 | GRCh38.p7 | 20:32961317 | ATACCACGGACAGCA[C/T]GCCTGCGGCCGCCTC | 388795 |
rs36036005 | snp | A/G | 0.0217752 | 0.102046 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874398 | TGGCTAATTTAAAAA[A/G]TTTTTTTTGTAGATT | 388795 |
rs36116924 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941316 | TGGAAAACAGTCTGG[-/G]CAGTTCCTCAAAAAT | 388795 |
rs41373347 | snp | C/G | 0.167158 | 0.235875 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923974 | TGAAACATAATGCAA[C/G]ATAGCAAAAGCTTTC | 388795 |
rs41492345 | snp | A/G | 0.165853 | 0.235413 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924479 | GAATGTATGTGAAAA[A/G]AATGTTTAATACATC | 388795 |
rs55681501 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867275 | ATATAGTTACTGAAC[C/T]GAGGTCCCTTATAAA | 388795 |
rs55836743 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952400 | CTCTTACTTTTTGGT[C/T]TATAATCATTTTGAG | 388795 |
rs55884127 | snp | A/G | 0.021333 | 0.101051 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872495 | AAGACAGACAGACAA[A/G]AGTGAAAGCGAGCTG | 388795 |
rs55888348 | snp | A/C | 0.434253 | 0.168969 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950020 | CAAACAAAACAACAA[A/C]ACAACAACAACAACA | 388795 |
rs55901614 | snp | A/C | 0.081446 | 0.184634 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926489 | TTTTCCTCTCAGCAC[A/C]TAATAATCTATCCAC | 388795 |
rs55952845 | snp | C/T | 0.46875 | 0.121031 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895575 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTA | 388795 |
rs56009141 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937168 | TATTTTTAGTAGAGA[C/T]AGGGTTTCTCCATGT | 388795 |
rs56031406 | snp | A/G | | | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32885613 | GCAGTTCTGGTCTGA[A/G]TCCTTCTCGCTGATG | 388795 |
rs56136077 | in-del | -/TTTCTTTCTTTC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939192 | TTCTTTCTTTCTTTC[-/TTTCTTTCTTTC]CTCTCTCTCTCTCTC | 388795 |
rs56154324 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959003 | CTGGCTACTTGGTCC[C/T]CCCCCTGCAGGTTCA | 388795 |
rs56175651 | snp | A/C | 0.434253 | 0.168969 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950014 | CAAAAACAAACAAAA[A/C]AACAAAACAACAACA | 388795 |
rs56222573 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945551 | GAGCATTTTTATTAC[A/G]GTTACTTAGAATTCT | 388795 |
rs56228321 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950008 | CTGTCTCAAAAACAA[A/C]CAAAACAACAAAACA | 388795 |
rs56260622 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921832 | TTTGTTACCTTATTC[C/T]TTTTTTTTTTTTTTT | 388795 |
rs56350771 | snp | A/C | 0.384976 | 0.210431 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950022 | AACAAAACAACAAAA[A/C]AACAACAACAACAAC | 388795 |
rs56865385 | snp | C/T | 0.39214 | 0.205661 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939484 | GAGACGGGGTTTCAC[C/T]GTATTGGTCACGCTG | 388795 |
rs56900670 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937633 | ATTTTTCTTTTTTTT[-/T]GTTGAGACAGAGTCT | 388795 |
rs56942213 | in-del | -/ATGCCCCTCTAGCTGTGAACCTGTGATGCTAACA | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913680 | TTCATTCTGAAGCAA[lengthTooLong]CGTTATGTACTTCCA | 388795 |
rs56972265 | in-del | -/TTTC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939200 | TTCTTTCTTTCTTTC[-/TTTC]CTCTCTCTCTCTCTC | 388795 |
rs57088373 | snp | C/T | 0.109108 | 0.206518 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928935 | GTTTTCTGCATCAAT[C/T]AAGATGATCGTGTGG | 388795 |
rs57106662 | snp | C/G | 0.26271 | 0.249677 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907109 | AAAGGCCTAGCAGGA[C/G]GGGCCCCGGGTGGGA | 388795 |
rs57383700 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896941 | TACCATGGCCGTCAG[A/G]ACGTGAGGTGATCTG | 388795 |
rs57469624 | in-del | -/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921392 | TGTGTGTGTGTGTGT[-/G]TTTTGTAGAGATGGG | 388795 |
rs57508978 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873654 | GATCACTTGAGGTCA[A/G]GAGTTTGAGAGCAGC | 388795 |
rs57551001 | in-del | -/AA | 0.0524604 | 0.153226 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944991 | TCTCATAAATCCCTT[-/AA]GTTTTCTTTACTCTT | 388795 |
rs57620114 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875520 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTTTTCT | 388795 |
rs57768611 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868025 | TTTTCTTTTTTTTTT[-/T]AGAAACAAGGGCTTG | 388795 |
rs58048875 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951024 | AGAAGAGAAATACTA[A/T]TTAAAACCGCTGTAA | 388795 |
rs58199286 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926686 | CCACAACAGTCCCCA[A/G]AGTGTGATGTTCCCC | 388795 |
rs58219086 | in-del | -/GT/TGTGTGTT/TGTGTT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921391 | GTGTGTGTGTGTGTG[-/GT/TGTGTGTT/TGTGTT]TTTTTGTAGAGATGG | 388795 |
rs58246133 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945835 | TACGCATGTAAATTC[A/G/T]CAATTACAGGAATCT | 388795 |
rs58410872 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934013 | AAAGCAAATCAAAAA[C/T]TTTTTTTTTTTTTTT | 388795 |
rs58684353 | snp | G/T | 0.0618563 | 0.164627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896765 | GTCCTGGCCGACACC[G/T]CCTCGCTCCTGGATG | 388795 |
rs59048766 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873668 | AGGAGTTTGAGAGCA[G/T]CCTGGCCAACATGAT | 388795 |
rs59079576 | in-del | -/A | 0.0107246 | 0.0724382 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951548 | TGGTTGTTTGAGGAT[-/A]GGGGGCTGATGAGGG | 388795 |
rs59381928 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950927 | GTGGCAGTGTTTGTC[C/T]GAGATGACGGTGCTC | 388795 |
rs59547049 | snp | C/G | 0.119978 | 0.213528 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937152 | TACCTGGCTAATTTT[C/G]TATTTTTAGTAGAGA | 388795 |
rs59567336 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892847 | TTTTTTTTTTTTTTT[-/T]CTTTTTTTTATGACT | 388795 |
rs59621948 | snp | A/G | 0.479095 | 0.100076 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912449 | AAAAAAAAAAAAGAA[A/G]AAGAAGAAAGAAAGT | 388795 |
rs59681625 | snp | A/G | 0.0205393 | 0.0992361 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32960092 | GGGAGCGGCGTATAA[A/G]CCCAAGGAACGCTTG | 388795 |
rs59817437 | in-del | -/GA | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948569 | AGAAAGAAAGAAAGA[-/GA]AAGAAAGAAAGAAAA | 388795 |
rs60039933 | snp | A/G | 0.109108 | 0.206518 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929019 | TCATCCTTGCATTCC[A/G]GGAATAAAAGTCACT | 388795 |
rs60272352 | snp | A/G | 0.0707826 | 0.174302 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940751 | CAAATTAAGATACGG[A/G]TAAAGGATCTAAATA | 388795 |
rs60305881 | in-del | -/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912446 | AAAAAAAAAAAAAAA[-/G]AAGAAGAAGAAAGAA | 388795 |
rs60358380 | in-del | -/AAAAAAAAAAAAA/AAAAAAAAAAAAAA | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905773 | CAAAAAAAAAAAAAA[-/AAAAAAAAAAAAA/AAAAAAAAAAAAAA]GGACATTCCTTTCCC | 388795 |
rs60484555 | in-del | -/TT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873645 | GAGAGGGCGGATCAC[-/TT]GAGGTCAGGAGTTTG | 388795 |
rs60562366 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900716 | GGACTACAGGTGTGC[A/G]CCACCATGCCCGGTT | 388795 |
rs60705670 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945664 | TTTTTTTTGTGTGCC[G/T]TATAACTTTATATTG | 388795 |
rs60863075 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877137 | AACTGCCGTCTCATA[A/G]CTCTCCTCAGCATAG | 388795 |
rs61235703 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956957 | CTTTTTTTTTTTTTT[-/T]CATTTTTTTTCAATC | 388795 |
rs62207460 | snp | G/T | 0.0956147 | 0.196779 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904318 | CTTTTTGTTTTTTTC[G/T]TGGACAGGTTCTTGC | 388795 |
rs62207462 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908864 | CAGGAGAGACCCTGT[A/G]GGAAACTGAGTCACA | 388795 |
rs62207463 | snp | A/G | 0.202343 | 0.245416 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909562 | CAGAAGTTATAAGGT[A/G]AAAGGGACCTTGGAC | 388795 |
rs62207464 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910149 | CTCCATCCGTTAGCC[A/G]TGGGATCGCCTAACT | 388795 |
rs62207465 | snp | A/C/G | 0.00874735 | 0.0655527 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917226 | CCCAGAATCCTCAAG[A/C/G]CTCCAGTGCTTCCCC | 388795 |
rs62207466 | snp | A/C | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920325 | GCCCGGCCTGATTCT[A/C]CCCAGTGCCCGGAAG | 388795 |
rs62207481 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939497 | ACTGTATTGGTCACG[C/T]TGGTCTCAAACTCCT | 388795 |
rs62207482 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953942 | CAGCCTCCCGAGTAG[C/T]TGGGCTTACAGGCCC | 388795 |
rs62207483 | snp | C/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953959 | GGGCTTACAGGCCCA[C/T]CACACCTCTCTAATT | 388795 |
rs62208880 | snp | C/T | 0.403334 | 0.197456 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875478 | AAGACTGCCTTGAAC[C/T]GAGCACACCTGGTAA | 388795 |
rs62208881 | snp | C/G | 0.0759472 | 0.179459 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876702 | CCGGGCACAGTGGCT[C/G]ATGCCTGTAATCCTA | 388795 |
rs62208882 | snp | A/G | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878172 | TCAGGAGGCTGAGGT[A/G]GGAGGATCACTTGAG | 388795 |
rs62208903 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891842 | GTTTTTTTTTTTTTT[A/T]AATTGAGACAGGGTC | 388795 |
rs62208904 | snp | C/G | 0.0298358 | 0.118439 | missense | EFCAB8 | GRCh38.p7 | 20:32892246 | ACCACAAATGTGTCC[C/G]GGCCTTCACCTTTGT | 388795 |
rs62208905 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893032 | TTTTAGTAGAGATGA[A/G]GTTTCACCACGTTGG | 388795 |
rs62208906 | snp | C/T | 0.289701 | 0.246828 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893130 | ACAGGTGTGAGCCAC[C/T]GCGCCCAGCCCACAC | 388795 |
rs62208907 | snp | A/G | 0.146314 | 0.227484 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897348 | AAAATAGTACCCTGC[A/G]CTTGGTGGGCTCCCA | 388795 |
rs62208908 | snp | G/T | 0.39709 | 0.20215 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897473 | GTTGAGTCAGGGCCT[G/T]ACTCTGCTGCCCTGG | 388795 |
rs62208909 | snp | C/T | 0.26326 | 0.249648 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900991 | ACAGGCATGAGCCAC[C/T]GCGCCCGGCCGTCCA | 388795 |
rs66499347 | snp | C/T | 0.308166 | 0.243139 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860890 | ACTACAGGGGAGTGT[C/T]ACCATACCCAGATAA | 388795 |
rs66909366 | snp | C/G | 0.314787 | 0.241459 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907796 | ATGCCTCCAAGAAGT[C/G]AGGGTCTTGGAGGGA | 388795 |
rs67018325 | in-del | -/T | 0.375 | 0.216506 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900363 | TCCAGTGCCTTTTTT[-/T]GTTTTGTTTTGTTTT | 388795 |
rs67198073 | in-del | -/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891834 | GTTGGAAGGAGTCAG[-/T]TTTTTTTTTTTTTTA | 388795 |
rs67434119 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912449 | AAAAAAAAAAAAGAA[-/G]AAGAAGAAAGAAAGT | 388795 |
rs67457409 | snp | A/G | 0.00993419 | 0.0697739 | missense | EFCAB8 | GRCh38.p7 | 20:32908386 | TTCTTCGAGAAGGAC[A/G]ATACCCTCATCTGCA | 388795 |
rs67619707 | snp | A/G | 0.249603 | 0.25 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941841 | GAGCACTTTAAATTG[A/G]TAAATTTTTATGTGA | 388795 |
rs67685654 | snp | A/G | 0.486398 | 0.0813386 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912446 | AAAAAAAAAAAAAAA[A/G]AAGAAGAAGAAAGAA | 388795 |
rs67842457 | snp | C/T | 0.146985 | 0.227789 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877914 | CTTAGCGCCTCAGGA[C/T]GGCGAGGGAGACGCT | 388795 |
rs68041883 | in-del | -/T | 0.319376 | 0.240181 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956957 | TCTTTTTTTTTTTTT[-/T]CATTTTTTTTCAATC | 388795 |
rs71190881 | in-del | -/AAAA | 0 | 0 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860521 | GTAAGACTCCATCTC[-/AAAA]AAAAAAAAAAAAAAA | 388795 |
rs71190882 | in-del | -/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874183 | CTATAATCCCAGTAC[-/T]TTTGGGAGGCTGAGG | 388795 |
rs71190883 | in-del | -/AAAAAAAAAAAAAAAAAAAA/AAAAAAAAAAAAAAAAAAAAA | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875503 | AGAAAACTTTGTTTC[lengthTooLong]AAAAAAAAAAAAAAA | 388795 |
rs71190885 | in-del | -/A | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934028 | AGACCTCATCTCTAC[-/A]AAAAAAAAAAAAAAA | 388795 |
rs71333800 | in-del | CTAAAGA/TTAAAG | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914911 | GTGAGATCCCATGTC[CTAAAGA/TTAAAG]AAAAAAAAAATGGAA | 388795 |
rs71337926 | snp | C/T | 0.402806 | 0.197864 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875590 | GCTCACTGCAACCTC[C/T]GCCTCCTGAGTTCAA | 388795 |
rs71337927 | snp | C/T | 0.193653 | 0.243567 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940049 | TTCCTTCCTTCCTTC[C/T]TTCCTTCCTTCCTTC | 388795 |
rs71348793 | snp | A/G | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865732 | TGAACCCAGGAGGCA[A/G]AGGTTGCAGTGAGCT | 388795 |
rs71348795 | snp | A/G | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931684 | AATCTCTTGAACCTA[A/G]AAGGCAGAGGTTGTA | 388795 |
rs71348797 | snp | G/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950819 | CAAGCTGTCCTATTG[G/T]ATTTTACTGTCTGCT | 388795 |
rs71858676 | in-del | -/TG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921362 | TATGCCCAGCTATTT[-/TG]TGTGTGTGTGTGTGT | 388795 |
rs72023434 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910760 | TTTTTTTTTTTTTTT[-/T]GCCAGGGTCTCGCTC | 388795 |
rs73114148 | snp | C/G | 0.0146672 | 0.084371 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859891 | AAATAACAGCCCTTG[C/G]AGCATTTTTGTTTTT | 388795 |
rs73114154 | snp | C/T | 0.293551 | 0.246177 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861580 | AGATGTGAGCCACCG[C/T]GCCTAGCCGTTGAAA | 388795 |
rs73114175 | snp | A/G | 0.021333 | 0.101051 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872496 | AGACAGACAGACAAG[A/G]GTGAAAGCGAGCTGG | 388795 |
rs73114189 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880878 | TCTGGGGCTGTGGGA[G/T]TTAGGAACTGTGGGC | 388795 |
rs73114195 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883495 | TAGCATGTCCAGTTC[A/G]TATAGCTTGAATGGC | 388795 |
rs73116348 | snp | C/T | 0.0599151 | 0.162381 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917548 | CCACCCTTCTCTCAG[C/T]TGTGAACCAGAATCC | 388795 |
rs73116352 | snp | A/C | 0.15698 | 0.23205 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921009 | ACACCCCTCACTGTG[A/C]TACTGACTCCCCGTC | 388795 |
rs73116377 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948065 | GGTTCTTTGAAAAGA[C/T]AGTTAAATCGATAAA | 388795 |
rs73116378 | snp | G/T | 0.0399052 | 0.1355 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948315 | TATCCTTATATCAAA[G/T]AAATTAAATTTGTAG | 388795 |
rs73116392 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957757 | GATTCTCATTCAGCC[C/T]GTGTGTAGACTCAGG | 388795 |
rs73249221 | snp | C/T | 0.030665 | 0.119967 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903353 | CCTTCTGTTGTCCTC[C/T]GTCAAAGCCATGTGC | 388795 |
rs73249223 | snp | C/T | 0.030665 | 0.119967 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905137 | CTGGATCGCTGCTTA[C/T]TGAGCTTCCTGCCAC | 388795 |
rs73249230 | snp | A/G | 0.108755 | 0.206276 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923772 | CATGACGGTGTTTAC[A/G]GAGCCATGGCATTCC | 388795 |
rs73249233 | snp | C/G | 0.1652 | 0.235179 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924457 | ATTTATTTAATACAT[C/G]TGAAAAGAATGTATG | 388795 |
rs73249236 | snp | A/G | 0.165853 | 0.235413 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924632 | GGTCTATTTGTTTTC[A/G]AAGTTCAAGTTCTTT | 388795 |
rs73249246 | snp | C/T | 0.109108 | 0.206518 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930008 | TTCACTATAGATATA[C/T]ATGAAGGGGAATGAG | 388795 |
rs73249247 | snp | C/T | 0.108755 | 0.206276 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932481 | TAAAAAGGCTTACAG[C/T]GAAGAGTCTAAGTCC | 388795 |
rs73249255 | snp | A/G | 0.109814 | 0.206997 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934547 | CCCATACTATTTCTC[A/G]TAGTGGTTGATATGG | 388795 |
rs73249264 | snp | C/T | 0.120326 | 0.21374 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944250 | TGTCCCCTTTTCCTC[C/T]TGTGCTGTCTTCCTA | 388795 |
rs73262372 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859836 | TTAATATGCTATCTA[A/G]TAATATAGAGTCCAT | 388795 |
rs73262379 | snp | A/G | 0.030278 | 0.119257 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861897 | CCAATATGCACATGC[A/G]TATATTCTTAACAGA | 388795 |
rs73262381 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861933 | ACTTAACATTTTACA[G/T]ACACTTTAGTTTTTT | 388795 |
rs73262394 | snp | G/T | 0.0592355 | 0.161582 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875446 | GACCAGCTGAGGACC[G/T]TAGGGGAGGCAGCAC | 388795 |
rs73615615 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869061 | CCACTTCCAAGCTCA[C/T]TCAGGTTGTTGGCAG | 388795 |
rs73615616 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874613 | GTGGTGCAATCTCGG[C/T]TCACTGCAACCTCTG | 388795 |
rs73615617 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882296 | CAGCCCTCCAAACAG[A/G]ATATCGTCCATTCAC | 388795 |
rs73615618 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900776 | GGTTTCACCATGTTG[G/T]CCAGGATGGTCTCGA | 388795 |
rs73615619 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945594 | TAATATACCTCAATT[C/T]CTTTAGCGGCAGTTT | 388795 |
rs73615620 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952869 | TAACCATTTTTAAGT[C/T]TACAGTTCAGTAGTG | 388795 |
rs73904057 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865220 | GTCATCTGAAAGTTA[C/T]GGAAGAGCTCCTTGG | 388795 |
rs73904058 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866648 | GGCAGGTGAGCTCAT[C/G]TGACCGAGATGGGAC | 388795 |
rs73904065 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887684 | TCTTCCCCAGGACAC[A/G]GCAGCTCATTTCTGC | 388795 |
rs73904066 | snp | G/T | 0.159292 | 0.232964 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890880 | TAGGTGTGTGAAGCT[G/T]CTGGCATAGTGCCTG | 388795 |
rs73904069 | snp | C/T | 0.0246229 | 0.10819 | missense | EFCAB8 | GRCh38.p7 | 20:32893271 | GGGCTGTTCAACCCC[C/T]GTATCCTCCCCAGGG | 388795 |
rs73904070 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896380 | CAAGCCAACTCAAGA[C/T]GTCTTCTGAGGCTTT | 388795 |
rs73904071 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897308 | AACGGCAGCGGCTTC[A/G]TGCTCTCGGTTGTCT | 388795 |
rs73904072 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898206 | TCTCTCCTCGTGGGA[A/G]ATGATTAGTATGGGC | 388795 |
rs73904074 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898802 | CTTTTATCTCCCAAT[C/T]TATATGCAAAACTCA | 388795 |
rs73904075 | snp | C/G | 0.0425829 | 0.139564 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901182 | GGAGCTGTTTGCTGA[C/G]GCTATCTGTCTGCAT | 388795 |
rs73904078 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910071 | CTTGATGGTGGTGCT[A/G]GGGCAGCGGGATAGA | 388795 |
rs73904083 | snp | C/G | 0.0283406 | 0.115616 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929857 | TCCCACTGTGGCCCC[C/G]ACATGGGCCACAGGT | 388795 |
rs73904084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930706 | CCTTGCCTAGTTCCT[A/G]CTCTGTCTGGGTACT | 388795 |
rs73904086 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942893 | TCATGTTTTCTGTTA[C/G]CACTCTTACTATATA | 388795 |
rs73904087 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943479 | GACCTATGTAAGGTC[A/G]CAAGCAAGTTCATGT | 388795 |
rs73904088 | snp | C/T | 0.029116 | 0.117091 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960216 | GGGGCCAGGGGATCC[C/T]ATGTCCACCAGCAGC | 388795 |
rs73904089 | snp | A/G | 0.0178098 | 0.0926698 | downstream-variant-500B | EFCAB8 | GRCh38.p7 | 20:32962009 | TGAGGACCGGCAGCC[A/G]TCTGGTGAGGGTCAT | 388795 |
rs73904090 | snp | A/G | 0.0115144 | 0.0749975 | downstream-variant-500B | EFCAB8 | GRCh38.p7 | 20:32962053 | CTGCCCCTGCTGTCT[A/G]TCAGTCTTCCCTCAT | 388795 |
rs74174545 | multinucleotide-polymorphism | CT/TC | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872495 | CCAGCTCGCTTTCAC[CT/TC]TTGTCTGTCTGTCTT | 388795 |
rs74339605 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905911 | GTCTCAAATGCCAAG[A/G]TGCCATATTTTGGGG | 388795 |
rs74342009 | snp | A/G | 0.0707826 | 0.174302 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885207 | CCTCTGTCCCATCAC[A/G]TCGCGAGGAGGCTGG | 388795 |
rs74463131 | snp | A/C | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882217 | AAAGAAAAAAAAAAA[A/C]AGCATGCAAATGCAA | 388795 |
rs74493370 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896886 | CAGTTGAGTCACCCC[A/G]GTAGCTTCTCATCAC | 388795 |
rs74546108 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885182 | TTTGCGAACAACCTC[C/T]GTTCTGTCTCCTCTG | 388795 |
rs74590750 | snp | A/C/G | 0.00755907 | 0.0610114 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863567 | ATCAGGGGAAGAAAG[A/C/G]CTCAAGTGCAAGCTT | 388795 |
rs74687305 | snp | A/C | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865795 | GTGAGACTCTGTCTC[A/C]AAAAAAAAAAAAAAA | 388795 |
rs74802861 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959482 | GGCAGGGGGCAGACA[C/T]GTTTAAATAGTCCAC | 388795 |
rs74849424 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929379 | AGCAGGTTGAACAAC[A/T]AATTTCGGATTTCTA | 388795 |
rs74862783 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866303 | TTGGCTTTTTGAACT[A/G]AAGTGTTTTCAACTT | 388795 |
rs74879023 | snp | A/C/G | 0.00557542 | 0.0525036 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868359 | TGAGCCACTGTGCCC[A/C/G]ACCCTGATCAGCATC | 388795 |
rs74895145 | snp | A/C | 0.0509478 | 0.151255 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883200 | TTTCTCTGATATCAC[A/C]CAAGACATCTGGGTA | 388795 |
rs74953036 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877114 | GGTGCCTTGAGAGTC[C/T]CTGCGTTAACTGCCG | 388795 |
rs74967441 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957330 | AATTAAAAAAAAAAA[A/C]CCCAAAACTTTTCTG | 388795 |
rs75006708 | snp | C/T | 0.0151459 | 0.0856945 | missense | EFCAB8 | GRCh38.p7 | 20:32961241 | CAAGACCAGCACATC[C/T]GCCTGGTGGCCCACC | 388795 |
rs75108384 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949641 | GTGCAAAGGCAATTC[A/G]GTGGAGAAAAGACAG | 388795 |
rs75110305 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907148 | AGGGTGGCCATGGAC[C/T]TCTGAGCATGTCCCC | 388795 |
rs75202799 | snp | G/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866940 | CGTTTCTTTTTTTTT[G/T]GAAGTCTTGCTCTGT | 388795 |
rs75263960 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919056 | GCCCCAGGACTAGCC[C/T]TTCCAAGAATGGCTG | 388795 |
rs75332537 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940128 | GTAAGAAAAAAATCT[C/T]GAGAAAGAACAGAGT | 388795 |
rs75408249 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955014 | CCTGGACATCTATCC[C/T]CCCCATGAGTAGAGT | 388795 |
rs75463208 | snp | G/T | 0.0225045 | 0.103662 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859085 | TGCCTGACCTCCAAG[G/T]CTGGAGAGCAGCTCT | 388795 |
rs75491169 | snp | G/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936744 | TGAAATCAGGGACTG[G/T]GATGTCTTTAGCTTT | 388795 |
rs75694022 | snp | C/T | 0.00676609 | 0.0577691 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860718 | CATAGTGTGCACCCT[C/T]TTCTGCATCTTGGTT | 388795 |
rs75713500 | snp | C/T | 0.00636936 | 0.0560724 | downstream-variant-500B | EFCAB8 | GRCh38.p7 | 20:32961985 | CTTGGTTCAGCCTCA[C/T]GGCAAGAGTGAGGAC | 388795 |
rs75724411 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912004 | CTAGCAGTGGGATCA[A/G]TTAATTCACAGCCAC | 388795 |
rs75795113 | snp | C/T | 0.00676609 | 0.0577691 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859774 | GTACATTTCCTGAAA[C/T]AAGGACATTCTCATA | 388795 |
rs75854523 | snp | G/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897456 | TTTTTTTTTTTTTTT[G/T]GGTTGAGTCAGGGCC | 388795 |
rs75947542 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948017 | AAACAGGGAAGTAAA[A/C]AATAATAAGGAAAAT | 388795 |
rs76059532 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944521 | TATTACAGTATTACA[A/G]CATTCTGTATTTTTC | 388795 |
rs76063829 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956097 | AATATTTAAAAAATT[A/G]TTGTTTTATGTCCTC | 388795 |
rs76081170 | snp | A/C | 0.0275645 | 0.114116 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889035 | CACGGCTCACTGCGG[A/C]AAGACTTTGATAGAA | 388795 |
rs76107714 | snp | G/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883709 | TTCTTTTTTTTTTTG[G/T]AGACGGAGTCTCACT | 388795 |
rs76120117 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893845 | CACCTCCCATAATCC[A/G]CCCCTACTGTCAGGA | 388795 |
rs76287246 | snp | G/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866941 | GTTTCTTTTTTTTTT[G/T]AAGTCTTGCTCTGTT | 388795 |
rs76404073 | snp | A/G | 0.0561177 | 0.157828 | missense | EFCAB8 | GRCh38.p7 | 20:32961238 | CAGCAAGACCAGCAC[A/G]TCCGCCTGGTGGCCC | 388795 |
rs76428896 | snp | C/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870875 | TTTTTTTTTTTTTTC[C/T]TGAAATGGAGTCTCA | 388795 |
rs76507784 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946308 | AGCTGGAAGCTGGTG[A/G]TTCCTTCCCAATCTG | 388795 |
rs76538728 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881769 | ACGAGTTCCAAACTC[A/G]CGAGCCATTTTTACC | 388795 |
rs76558616 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876688 | TACCTCTATTTCGGC[C/T]GGGCACAGTGGCTCA | 388795 |
rs76559742 | snp | G/T | 0.0655868 | 0.168795 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929143 | TCTCTGTAGTCTTTT[G/T]TTTTTTCTTATAATG | 388795 |
rs76561249 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955727 | GTTCCACGTCCTGAG[C/T]GAGGGTATAGGTGGC | 388795 |
rs76585286 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913573 | CAATAGCCCAAAAGT[C/G]TTAACTTGTTCCAGT | 388795 |
rs76656637 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937267 | TTAGAAGCATGAGCC[A/C]CTGCCCACTGCACCT | 388795 |
rs76669312 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880534 | CCTTGGCCTCCCAAA[A/C]TGCTAGGATTATAGG | 388795 |
rs76701260 | snp | C/T | 0.031825 | 0.122064 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889022 | GCAGTGGTGTGTTCA[C/T]GGCTCACTGCGGCAA | 388795 |
rs76707071 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944518 | CACTATTACAGTATT[A/G]CAGCATTCTGTATTT | 388795 |
rs76716198 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952606 | ATTTTGTTGTTTTTA[A/G]GAAATTTGGTTGCTT | 388795 |
rs76736644 | snp | C/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949946 | CGGAGGCTGCAGTGA[C/G]CCAAGATCGCACCAC | 388795 |
rs76814865 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955673 | TGAGAAGGGGGCTGG[A/G]AGCCTTCCCCACCTC | 388795 |
rs76814988 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896283 | TTTCCTGGGGTGGGG[A/G]CACTCCGCTCAGCTC | 388795 |
rs76855067 | snp | A/C | 0.0681886 | 0.171594 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897344 | GCCTAAAATAGTACC[A/C]TGCGCTTGGTGGGCT | 388795 |
rs76872984 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892073 | GGTTTACTCTGTGAA[C/T]AGCTGTCTGTGGTTG | 388795 |
rs76944458 | snp | C/T | 0.109108 | 0.206518 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930035 | TGAGTTCCTTCCCCA[C/T]ATCACTTTGGGTTGA | 388795 |
rs76961155 | snp | A/G | 0.0456336 | 0.143994 | utr-variant-3-prime | EFCAB8 | GRCh38.p7 | 20:32961827 | TGTTCTCAGCTGTGG[A/G]CATCCACAGGTGATG | 388795 |
rs76963583 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881864 | CACCCCCATCAGGCC[C/T]TTAGGGAATTCTGAC | 388795 |
rs77179483 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948808 | TTGACAAAATTCAAC[A/G]TCCATTTCTGATAAA | 388795 |
rs77217585 | snp | C/G/T | 0.0279526 | 0.114869 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864942 | AGGTCTCAACCACAG[C/G/T]CCTGCAGGGTAGGGA | 388795 |
rs77282238 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948016 | GAAACAGGGAAGTAA[A/C]AAATAATAAGGAAAA | 388795 |
rs77299349 | snp | G/T | 0.0663309 | 0.169604 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930154 | GTGTCAGGCACCATT[G/T]TGGTTACTAAGGACA | 388795 |
rs77322737 | snp | A/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870376 | TCCAAACGGTTCAAA[A/T]TCCAAAAGGTACTTT | 388795 |
rs77376603 | snp | A/G | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862328 | AGATGTGGGGTCTCA[A/G]TGTTGCCCAGGCTGG | 388795 |
rs77409830 | snp | G/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862148 | TCTTTTTTTTTTTTT[G/T]GAGACAGGGTCTCAC | 388795 |
rs77414778 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907157 | ATGGACCTCTGAGCA[C/T]GTCCCCAGAGCTGGG | 388795 |
rs77421550 | snp | G/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883707 | ATTTCTTTTTTTTTT[G/T]GGAGACGGAGTCTCA | 388795 |
rs77467549 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912572 | AGCTATCCTCTCTGT[A/G]AAATGGACATGGATG | 388795 |
rs77524358 | snp | C/T | 0.00782141 | 0.0620446 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32896486 | TCCTTGCAGAAACTC[C/T]TAAATGAGAAGTCTG | 388795 |
rs77576885 | snp | C/G | 0.0345262 | 0.126772 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955846 | TTTGTTAAAAACGAC[C/G]CTTTCAGCCCATCTC | 388795 |
rs77680856 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958778 | AGCTGAAAGGTTGAG[C/T]AGTGAAAGGGGAAAA | 388795 |
rs77683107 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862651 | TATTTTTTTGGGACA[G/T]AGTCTTGCTCTTGTT | 388795 |
rs77720743 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890220 | CTGTGGTGCTGAGGC[C/T]ACTGTGGTCTCCTCT | 388795 |
rs77734517 | snp | C/G | 0.0402882 | 0.136092 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949705 | ACCACATACAAAAAG[C/G]AATTCAAAATGGGCC | 388795 |
rs77772074 | snp | A/T | 0.0295035 | 0.117819 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938433 | CCACCCCAATTTAAC[A/T]TTTTATTGGGAGGTC | 388795 |
rs77935188 | snp | A/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941821 | AATACTAAAAACCAT[A/T]GAATGAGCACTTTAA | 388795 |
rs78150898 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929983 | ATGATTGGCTGGAAA[A/G]TATGGATATTTCACT | 388795 |
rs78156973 | snp | C/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870873 | TCTTTTTTTTTTTTT[C/T]CCTGAAATGGAGTCT | 388795 |
rs78178170 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914591 | AGGAAACTTACAATC[A/C]TAGTTAAAGGTGAAG | 388795 |
rs78206940 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917900 | ACAGTCTCCAAATTC[C/G]CATATCTCAGCAGAT | 388795 |
rs78207337 | snp | A/G | 0.109108 | 0.206518 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930747 | GTGAAACAATGCAGC[A/G]AGGAGTCCTCTCCTG | 388795 |
rs78351341 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909754 | TTGGAAGTTTTTCCC[A/G]GCAGCCCATCACTGT | 388795 |
rs78461167 | snp | C/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940003 | CCTGCCTGCCTGCCT[C/G]CCTCCCTCCCTCCCT | 388795 |
rs78476151 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954478 | CTCTCTTCTATTCCA[C/T]TGGTTTATATGTCTG | 388795 |
rs78476944 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922486 | ATATCAAGCCCCTGA[C/T]CTCTGGAGCTGTCAT | 388795 |
rs78526194 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881881 | TAGGGAATTCTGACA[A/G]CGTTTTAAAACATGG | 388795 |
rs78585980 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872240 | TGGTGCTACCACTTA[C/T]CAGCTGTGTGACCTT | 388795 |
rs78719806 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862139 | TATTTCTTTTCTTTT[C/T]TTTTTTTTTGAGACA | 388795 |
rs78727522 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903605 | TTCCAGAACATTTTT[C/T]GGCAGCACATATACG | 388795 |
rs78742898 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957494 | AGGAGGACTCAGTTT[G/T]CCTCTGTGTTCAGTT | 388795 |
rs78755076 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918049 | CTCAGCTTTTTATCT[A/G]TTTTATGCTTTGGAG | 388795 |
rs78806222 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906354 | TGGGCTGCTGCTTTG[C/T]CTGTGGTGCTGAGCC | 388795 |
rs78880467 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944972 | TATTGTCCATTTGAC[A/G]ATGTCTCATAAATCC | 388795 |
rs78951406 | snp | G/T | 0.0637235 | 0.166737 | missense | EFCAB8 | GRCh38.p7 | 20:32909876 | TCAAAGCAAGGAAGA[G/T]GACCACTCATTGCTC | 388795 |
rs79004359 | snp | C/G | 0.000369038 | 0.0135788 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32918445 | GTGGACATACAAGAC[C/G]TCCAGGAAGCTCTCC | 388795 |
rs79029642 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897770 | TCCAGGTCTCACTCA[A/G]TGTCTTGGATTCGGT | 388795 |
rs79039358 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898035 | GTGGTTCAAGTTGCC[A/G]TGAAATGCACATTCT | 388795 |
rs79191182 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910226 | ACTGGGCCTTCTTGA[G/T]GTGGAGTATGAGACA | 388795 |
rs79255477 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859796 | ATTCTCATAACCACA[A/G]TACAGTTATCAAAAG | 388795 |
rs79351272 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950339 | TCAACAAGGAAACAA[A/G]TAATACAATAAAAAC | 388795 |
rs79396789 | snp | C/T | 0.021333 | 0.101051 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902828 | CTTCCTTGCAGCCAG[C/T]CTCACCTGAGTTCTC | 388795 |
rs79512448 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948015 | TGAAACAGGGAAGTA[A/C]AAAATAATAAGGAAA | 388795 |
rs79543061 | snp | A/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944473 | CTGTCTAAAAAAAAA[A/T]TAATAATAAAAATAA | 388795 |
rs79567865 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953613 | ATGTGCTTGTTGGCC[A/G]TTGTATATCATCTTT | 388795 |
rs79647810 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917942 | GGGACCTTAGGGGCC[A/G]CCTCATCCAGGGGTT | 388795 |
rs79683504 | snp | C/G | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886508 | CTGCAGAGTGATTCA[C/G]AGTTGCATCAGGGCT | 388795 |
rs79776594 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960743 | TAAATGAGATAACAC[C/T]GAAGGCCATGCCCCT | 388795 |
rs79888315 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946836 | CAGCCATTGATCTGT[C/T]TGTCTCTATAGTTTT | 388795 |
rs79968751 | snp | A/C | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882216 | AAAAGAAAAAAAAAA[A/C]CAGCATGCAAATGCA | 388795 |
rs79973939 | snp | C/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875591 | CTCACTGCAACCTCT[C/G]CCTCCTGAGTTCAAG | 388795 |
rs80003548 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861102 | GGAAGTCAGATTCAT[C/T]CTTCTGATGTTTGGG | 388795 |
rs80028098 | snp | G/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863995 | GTATTTTTTTTTTTT[G/T]AGACAGAGTCTCGCT | 388795 |
rs80057366 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952659 | GAAATTCTTTGTGTC[C/T]TGGATATGAGACCTT | 388795 |
rs80167635 | snp | A/T | 0.120674 | 0.21395 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936020 | TTTGCTTTTATTTAT[A/T]TTTATTTTTATTTTT | 388795 |
rs80219971 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948019 | ACAGGGAAGTAAAAA[A/G]TAATAAGGAAAATCA | 388795 |
rs80275195 | snp | G/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934028 | CTTTTTTTTTTTTTT[G/T]GTAGAGATGAGGTCT | 388795 |
rs80346332 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942894 | CATGTTTTCTGTTAC[C/T]ACTCTTACTATATAC | 388795 |
rs111239307 | snp | A/G | 0.0752113 | 0.178743 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862732 | TCCCAGGTTCAAGCA[A/G]TCCTCCTGCCTCAGC | 388795 |
rs111260829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862879 | CTCAGGCAATCCTTC[C/T]GCCTTGGCCTCCCAA | 388795 |
rs111265446 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875736 | CTGGTCTTGAACTCC[G/T]GACCTCAAGTGATCC | 388795 |
rs111334263 | snp | A/G | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932906 | TGTTATGGCTAGTTC[A/G]TTTTAGTATGAAGAG | 388795 |
rs111337378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924302 | CTTCTGGGCTCAAGC[A/G]ATCCTCCTGCCTTGG | 388795 |
rs111341382 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887180 | TTCTGATTATCCATC[G/T]AGAGGAATTGGTTTA | 388795 |
rs111345045 | snp | A/G | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869348 | TCAAGCGATTCTCCT[A/G]TCTCAGCCTCCCAAG | 388795 |
rs111348902 | in-del | -/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929139 | TATTTCTCTGTAGTC[-/T]TTTTTTTTTTCTTAT | 388795 |
rs111353081 | snp | C/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904284 | AGGCGTGAGCCACTG[C/T]GTCTGGCCTGAATAG | 388795 |
rs111366042 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892710 | CTGGTCTCCTGGGCC[C/T]GTGTTTGTTGGCTCC | 388795 |
rs111374733 | snp | C/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886862 | ATGCAGATGGAGACA[C/T]CTCAAGTTTGAGGCG | 388795 |
rs111377889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923849 | TAGCTATCTGCTGCC[A/G]CTGGGTTTTGCCTCT | 388795 |
rs111431717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925605 | TGATCCTCCTGCCTC[A/G]GCCTCCCAAAGTGTT | 388795 |
rs111610316 | snp | A/G | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877915 | TTAGCGCCTCAGGAC[A/G]GCGAGGGAGACGCTG | 388795 |
rs111641731 | snp | A/G | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901021 | AGTGCCTTTTTAACC[A/G]AACAGTGCACTGTGT | 388795 |
rs111654224 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910205 | AGCGCCTTGGGTCAG[C/T]TCTGGACTGGGCCTT | 388795 |
rs111662738 | snp | C/T | 0.031825 | 0.122064 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926666 | CCCTCCCCCCTCCCC[C/T]GACCCCACAACAGTC | 388795 |
rs111666616 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925886 | TTCAGTCCAGCAGCT[C/G]TTTCCAAAATGAGCA | 388795 |
rs111692588 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870343 | TGAATAGGTAATATA[C/T]CCACACAGTTCAATA | 388795 |
rs111757916 | snp | A/C | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950021 | AAACAAAACAACAAA[A/C]CAACAACAACAACAA | 388795 |
rs111775359 | snp | C/T | 0.183886 | 0.241099 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924129 | CACAATCACAGCTCA[C/T]TGTAGCCTCCACTTC | 388795 |
rs111874691 | in-del | -/A/AT/TA | 0.414097 | 0.250321 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926520 | TCATTCTTTTTTTTT[-/A/AT/TA]TTATTATACTTTAAG | 388795 |
rs111901164 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899417 | CTCAAAAAAAAAAAA[A/G]AAAAGAAAAACCAAT | 388795 |
rs111918410 | snp | A/G | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32958421 | CTGGTCAAATCACAG[A/G]AACGTTTGGCCTGAG | 388795 |
rs111933921 | snp | C/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950094 | ACTTCCAGAAGAAAT[C/T]GTAGGAGAAAACCTT | 388795 |
rs111962057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862379 | GCGATCCTCCCGCCT[C/T]GGCCTATTTTTTATT | 388795 |
rs111964129 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890970 | GAGAAAGTGGTCAGC[C/T]GTCAGCAAGGGCTAG | 388795 |
rs111981494 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877318 | GGTTCAAGTGATTCT[C/T]CTGCCTCAGCCTCCC | 388795 |
rs111996159 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894859 | ATGATTAAACCACAG[C/T]GCATCATAAAGCTGA | 388795 |
rs112004699 | in-del | -/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949203 | GAAATTGAAGTAAAA[-/G]ATACATTTACGAAAA | 388795 |
rs112011712 | snp | C/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872626 | TGGTGAAACCCTGTC[C/T]CTACTAAAAATACAA | 388795 |
rs112014354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945666 | TTTTTTGTGTGCCTT[A/G]TAACTTTATATTGGG | 388795 |
rs112046846 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919708 | TTCACCATGTTGGCC[A/G]GGCTGGTCTCAGACT | 388795 |
rs112065916 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914670 | AAACTGCCACTTTTA[A/C]ATCATCAGGTCTTGT | 388795 |
rs112138965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924571 | GTGAAGTGACTTGCC[C/T]AAGATTCTTATGGCC | 388795 |
rs112219262 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878098 | TGGCGAAACCCCATC[G/T]CTACAAAAAATACAA | 388795 |
rs112220231 | snp | C/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945903 | TCTCTCTGGTGTCTA[C/T]TTGCAGTACTGCAAG | 388795 |
rs112227952 | in-del | -/A | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894949 | CCCTCCCTGGGACTT[-/A]ACTTTGCAAGCTTCC | 388795 |
rs112231130 | snp | C/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932317 | GGGAGGTGGAGGTTG[C/T]AGTGAGCCTAGATTG | 388795 |
rs112240916 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884659 | CCCTGGAGGAGGGGT[C/T]ACAGTGCCTAGGTTC | 388795 |
rs112256176 | snp | A/G | 0.108755 | 0.206276 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933849 | CAGGCATGGTGATGC[A/G]TGCCTGTAATCCCAG | 388795 |
rs112264542 | in-del | -/A | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924228 | TGTGCCTGGCTCATT[-/A]AAAAAAATATATATT | 388795 |
rs112322903 | snp | G/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921132 | CCCTGAGAGCTGGGT[G/T]TTGCAGTGTTGGGAG | 388795 |
rs112332971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949145 | GATACAAGATCAATA[C/T]AAAAAATCAATTGTA | 388795 |
rs112334386 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909221 | TTTCTTGAGAAGGTA[C/G]TGGGTTCCTTTATCT | 388795 |
rs112335853 | snp | C/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900652 | GCTCACTGCAACCTC[C/T]GCCTCTCGGGTTCAA | 388795 |
rs112389446 | in-del | -/T | 0.30468 | 0.268226 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914900 | TAAGTTCTGCTTCCA[-/T]ATTTTTTTTTTCTTT | 388795 |
rs112399440 | snp | A/G | 0.00795532 | 0.062565 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860479 | TCATTTTGTTCCATC[A/G]CTGATGGTGGTAACT | 388795 |
rs112414936 | in-del | -/G | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877568 | ACAATGAGGCCAACT[-/G]AAAGAAAAAGAATAA | 388795 |
rs112479589 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879194 | CATCATAGGGGCACA[C/G]GTGGCACAGGTGGCC | 388795 |
rs112486247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925966 | TGGTTACCTGTCCCT[C/T]GCAGCCACACGGCTC | 388795 |
rs112549717 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932473 | AGGTAACGTAAAAAG[G/T]CTTACAGCGAAGAGT | 388795 |
rs112564207 | snp | A/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876502 | CTAAACGTTCGACAA[A/T]GGGAATATACAGCTT | 388795 |
rs112564585 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931484 | GTATTCGTGGCCAGT[C/T]GTGGTGGCCCACGCC | 388795 |
rs112564966 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945779 | TGGCTAAAGATTCTG[A/G]GTGCCTCCCCAATCT | 388795 |
rs112572809 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938526 | ATCTGCAGATGACAT[A/G]ATCTTATATCTAGAA | 388795 |
rs112577262 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923198 | CTTAAACAAACAAAC[A/C]AACCTGGCCCAGTGC | 388795 |
rs112581078 | snp | C/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912355 | CTGAGGCAGGACAAG[C/T]CGGGAGGTGGAGGCT | 388795 |
rs112668904 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897522 | ATCATGGCTCACTGC[A/G]GCCTTGACCTCCCGG | 388795 |
rs112731107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943574 | CTGCAGTCCTGGGTG[C/T]CTTCTAATTAGCCTG | 388795 |
rs112769170 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864336 | CACCTGTAGTCCCAG[C/G]ACTTTGTGAGGTGAA | 388795 |
rs112798506 | snp | C/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926599 | TGTGCCATGCTGGTG[C/T]GCTGCACCCACTAAC | 388795 |
rs112808309 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870230 | GGGTGGTGGTCTTCA[A/G]TGTCATTGTTTGCAG | 388795 |
rs112814652 | snp | C/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937478 | AACTACTAAAGCTGA[C/T]TTAATAAGAAATAGA | 388795 |
rs112816499 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868953 | TCATGCCACTTTACT[C/T]CAGCCTAGACCACAG | 388795 |
rs112821986 | snp | C/G | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925814 | GGAGGCCATTAACCC[C/G]CTGTGGTTGAGATAC | 388795 |
rs112834402 | snp | C/T | 0.0064249 | 0.0563131 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889446 | TCTGCTCTCAGCCAC[C/T]GGGAGCCATGCATTT | 388795 |
rs112834669 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891584 | AGCTGTCATCTGCTC[A/G]GAGGTACTCAGACAA | 388795 |
rs112851390 | snp | A/G | 0.0755793 | 0.179102 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865719 | CACGAGAATCACTTG[A/G]ACCCAGGAGGCAGAG | 388795 |
rs112853872 | in-del | -/T/TT | 0.498459 | 0.0277128 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934013 | AAGCAAATCAAAAAC[-/T/TT]TTTTTTTTTTTTTTT | 388795 |
rs112912697 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883899 | TTTCACCACGTTGGC[C/T]GGGCTGGTCTTGAAC | 388795 |
rs112967541 | snp | C/T | 0.130008 | 0.219321 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941169 | AGGCAGGAGAATCGC[C/T]TGAACCTGGGAGGCG | 388795 |
rs113027592 | snp | A/G | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907958 | GCAAGGGAGGGCCTG[A/G]GGCCAGCATGTGCTG | 388795 |
rs113033385 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910654 | TCAGTACCTTAAAAA[A/G]GTTTGTTTAAAATTT | 388795 |
rs113036635 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921790 | TGGATATACTTTCAT[G/T]AGAGGGATTTAGATT | 388795 |
rs113037350 | in-del | -/TGTT | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944267 | TGCTGTCTTCCTATG[-/TGTT]TGTTTGTTTGTTTGT | 388795 |
rs113114574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957808 | GCAGCTCCCACTCCC[A/G]GCTCTTCTTGGAAAG | 388795 |
rs113128522 | snp | G/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942556 | AATATATTAAAAGAT[G/T]AACTGATTGTCTATC | 388795 |
rs113131912 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950053 | AAAAATGGAACATAG[A/C]ACTAAAGGCAAAAGT | 388795 |
rs113138806 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912386 | GCAGTGAGCCGAGAT[C/T]CCGCCATCGCACTCC | 388795 |
rs113151698 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879670 | GATAGGACAGAGGGG[C/T]GATGAGCCAAGCGTA | 388795 |
rs113177878 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897811 | CGACAGATGCTTGGT[C/G]ACAGTGTGTGTAAAA | 388795 |
rs113180434 | in-del | -/TG/TGTGTGTG | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921361 | TATGCCCAGCTATTT[-/TG/TGTGTGTG]TGTGTGTGTGTGTGT | 388795 |
rs113257709 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862230 | CAACCTCCTGGGCTC[A/G]AGTAATTCTCCCACC | 388795 |
rs113259902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929621 | TGCTAGGATTACAGG[C/T]ATGAGCCACCATGAG | 388795 |
rs113305339 | snp | A/G | 0.295599 | 0.245806 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900660 | CAACCTCCGCCTCTC[A/G]GGTTCAAGCAGTTCC | 388795 |
rs113341957 | snp | C/G | 0.00177305 | 0.0297217 | missense | EFCAB8 | GRCh38.p7 | 20:32912837 | TGTTCTATGTGACAG[C/G]ATGGAGTAAGAGAAT | 388795 |
rs113345963 | snp | A/C | 0.0962929 | 0.197165 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877199 | TTCTTGTTTTTATTT[A/C]TTTCTTTCTTTTTTT | 388795 |
rs113346630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931981 | TTTTTGTTGGGGGAG[C/T]GGAGAGGCTGGAAGG | 388795 |
rs113349207 | snp | A/G | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945902 | CTCTCTCTGGTGTCT[A/G]TTTGCAGTACTGCAA | 388795 |
rs113378120 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952689 | TTAACAGGTATCCAC[A/C]TTGTGAGTACTTTTA | 388795 |
rs113412931 | snp | C/T | 0.110519 | 0.207473 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927591 | CTCAGGTGATCCACC[C/T]GCCTTGGCTTCCCAA | 388795 |
rs113425978 | snp | A/T | 0.0197687 | 0.0974348 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860469 | GTGATGGATGTCATT[A/T]TGTTCCATCGCTGAT | 388795 |
rs113448860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938474 | GAAAATGAAATAAAA[A/G]GTATCTATATTGGGG | 388795 |
rs113452924 | snp | C/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949927 | ATCGCTTGAACCTGG[C/G]AGGCGGAGGCTGCAG | 388795 |
rs113453076 | snp | A/C | 0.00642392 | 0.0563089 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878846 | TGGTGGGTGGGGTGA[A/C]TGGACAAGTGCTGGT | 388795 |
rs113529742 | snp | A/T | 0.0655868 | 0.168795 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952449 | TGAAATATGAGACAA[A/T]ATTTAAATTTTGCAT | 388795 |
rs113530961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943203 | GGCCCCATCACTTTC[C/T]AGCTATGTGGGCTTA | 388795 |
rs113532975 | snp | C/T | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944276 | TCCTATGTGTTTGTT[C/T]GTTTGTTTTAGTGAC | 388795 |
rs113566175 | snp | A/G | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935570 | GGAGTGCAATGGCGC[A/G]ATTGCAGCTCACCAC | 388795 |
rs113568081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865322 | TGTATGGGAGACACA[C/T]GTGAGTAAGCACCGA | 388795 |
rs113609938 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872515 | AAAGCGAGCTGGGCA[C/T]GGTGGCTCATGCCTG | 388795 |
rs113619711 | snp | A/G | 0.0741063 | 0.177655 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888051 | ATGGCTATCCTCTCT[A/G]CATATCCCCCTTTTC | 388795 |
rs113650019 | snp | A/G | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929287 | CTTAAATGTTTGGTA[A/G]AATTCACTGGTGAAG | 388795 |
rs113652177 | snp | C/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878569 | AGGTCGGACTGCGGA[C/T]TGCAGTGGCGCAATC | 388795 |
rs113676086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955775 | TAAAGGTCCTGCCTC[A/G]CATGTGCAAATGCTG | 388795 |
rs113741459 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874656 | AAGTGATTCTTGTGC[C/G]TCAGCCTCCCAAGTA | 388795 |
rs113752307 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941989 | TCCCAAGGAAAGAGT[A/T]TGTAAAAGAACATAA | 388795 |
rs113758406 | snp | A/G | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960988 | CCGCAGGCCACGGTG[A/G]TTAGTGGTAGCCACA | 388795 |
rs113759400 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903712 | TTTAGAGGAATCCTT[C/G]TGTCTCTGGACAGAT | 388795 |
rs113763775 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892358 | CCTCCTGCAGCAGCC[A/G]CATCACTGACTAGGG | 388795 |
rs113840053 | snp | A/G | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945930 | CAAGTTCTCTAGAGC[A/G]GCTACAAGCTTCCCC | 388795 |
rs113891250 | in-del | -/AA | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899420 | AAAAAAAAAAAAAAA[-/AA]GAAAAACCAATTAAT | 388795 |
rs113894602 | snp | C/T | 0.0733688 | 0.176922 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908528 | CTGGGACTGCTGAAG[C/T]GGCTAGACTCTGTGG | 388795 |
rs113952755 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940748 | AACCAAATTAAGATA[C/T]GGGTAAAGGATCTAA | 388795 |
rs113956360 | snp | A/G | 0 | 0 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860587 | TCTTAGTTCACTGCA[A/G]CCTCCACCTCCTGGG | 388795 |
rs113957003 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872398 | CCTCAGGGGACCAAT[A/G]TTTGTTGAAGCCAGG | 388795 |
rs113957875 | snp | A/G | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928531 | TGAGCCACCGCACCC[A/G]GCCAATGCGACTGAT | 388795 |
rs114057854 | snp | C/G | 0.0741063 | 0.177655 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908257 | TGCTCAGCGTCTTGC[C/G]TTTTTCCCATCCCCC | 388795 |
rs114124961 | snp | A/G | 0.0027196 | 0.0367751 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918623 | CACTCTCTAGCCGCC[A/G]GCGTTCACACACCGT | 388795 |
rs114125197 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877741 | TGGAGTCTGGAGTTG[C/T]GCCAGTGGCCCTGGT | 388795 |
rs114176944 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912000 | ATTTCTAGCAGTGGG[A/G]TCAGTTAATTCACAG | 388795 |
rs114242254 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919125 | AGGAGTTACTGTTTC[C/T]CTACTTGCAGGGGAT | 388795 |
rs114287156 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867821 | TACCTGGGGTGTGTG[A/G]AGGGTTCAGACATAA | 388795 |
rs114299583 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889569 | AGGCAGGGGGTGGTC[A/G]GTGAATGCTCGAATG | 388795 |
rs114778998 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918883 | AAAATTGGATGTTAG[A/G]TCCTGGGCTGCATTC | 388795 |
rs114813053 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914336 | GCTGGTGATGGGAGG[A/G]ACAGTCCTGATGATC | 388795 |
rs114827239 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898154 | GGCTCCCTGTGGATA[A/G]CTAGATTGTGGCCTG | 388795 |
rs114827421 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881126 | CAGGTTCCAAAAGCC[A/G]GAGTTGGCTTGGCAA | 388795 |
rs114834509 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915965 | GCATGAGCCACCCTG[C/T]CCAGCTGCTGTTACC | 388795 |
rs114836038 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951576 | GGGTTGGAAGGGTGG[A/G]AGCTCAAAGAAGCAG | 388795 |
rs114899916 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950664 | TGCAGGCAAATCCCC[C/T]GGGTTGCTTTTAGCT | 388795 |
rs114908276 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910214 | GGTCAGCTCTGGACT[C/G]GGCCTTCTTGATGTG | 388795 |
rs114916017 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891650 | TCCCCGGCCTTTGTG[A/G]CCCCAGCCCAGTCCA | 388795 |
rs114964645 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899022 | ATTGGTTCTTTGCAG[A/G]TGGTTCCAATCTGTT | 388795 |
rs114994575 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871747 | TCTTAGGCACCCCAA[C/T]TGTCACTGCGTGCCT | 388795 |
rs114995005 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946397 | CAGTGCAGCTGGTTT[C/T]TTGTTTTTTGTTTTT | 388795 |
rs115006345 | snp | C/T | 0.00184621 | 0.0303265 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911739 | AATTACAGCCAGGGA[C/T]GGCCTCTTGGGAAGC | 388795 |
rs115029632 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939588 | TCGCCTGGCGGGCTG[A/G]CTTTCTTTTCTTCCT | 388795 |
rs115034703 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910792 | GTCGCCCAGGCTGGA[A/G]TGCAATGGGACCTTG | 388795 |
rs115075421 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907350 | CAATGCATGGCAGCC[A/G]TTCCCCTGCGCTGCC | 388795 |
rs115108318 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918309 | CTGGGGCAGTCCTGA[A/G]TTTACCTCTACGACA | 388795 |
rs115118845 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930787 | GCCCAGTGACAGGAG[C/T]GGGTCTTGGTTCAAA | 388795 |
rs115154122 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905802 | CCCTAGGTATAGGTA[C/T]AGAGTGGGCACCTAT | 388795 |
rs115226398 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942630 | AATTTTATTTATGAT[C/G]ACTTAAAAATTACAA | 388795 |
rs115270238 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865308 | GATGGGTTGGACTGT[A/G]TATGGGAGACACACG | 388795 |
rs115278853 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907119 | CAGGAGGGGCCCCGG[A/G]TGGGAGGAAGGTGAG | 388795 |
rs115293998 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955497 | GTGAGTTAAGACTGC[A/G]CTGCTGTACTCCAGC | 388795 |
rs115322040 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878995 | TTAGGACTAAGGTAC[A/G]TGATTTGTCCCCATT | 388795 |
rs115361607 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880413 | AGCTGGGATTACGAA[C/T]GCCTGCCACCATGCC | 388795 |
rs115408339 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862973 | CATTTTGTTCAGACT[C/G]TCTGGCCAGGTATTC | 388795 |
rs115490400 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952217 | ATGCAGTAATCTGTG[A/G]TTGAGCCACTGCACT | 388795 |
rs115503987 | snp | C/T | 0.0209421 | 0.100162 | downstream-variant-500B | EFCAB8 | GRCh38.p7 | 20:32962239 | CTGGGCCATCAGCCC[C/T]CTTGGCAGCTGGAGA | 388795 |
rs115571893 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938511 | AAGTTAACTATCTCT[A/G]TCTGCAGATGACATA | 388795 |
rs115616802 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915559 | ATATTGAGGCTTTCT[C/T]TGCATCTGTCCTCTT | 388795 |
rs115622979 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947085 | ATTATGAATGAAGCC[A/G]CTTTAAACATTGTTT | 388795 |
rs115695065 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911769 | CAAAGCACAGCTCCT[A/T]TGACCCTGGGATGCA | 388795 |
rs115733121 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957287 | ATTGGTTATATTGGC[C/T]TTTTCACATGTCATA | 388795 |
rs115733646 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915999 | TTCTAAAGCCACTTC[C/T]CACATTTTTAGGTAT | 388795 |
rs115735517 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911393 | TTCTCAGTGGATGGA[G/T]GGGAGGGGCCAAGGC | 388795 |
rs115848167 | snp | A/G | 0.00661689 | 0.0571372 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32961141 | TTCCCTGCAGATCTC[A/G]CCTCAGGTCTACCAA | 388795 |
rs115908161 | snp | A/G | 0.00329675 | 0.0404661 | missense | EFCAB8 | GRCh38.p7 | 20:32867732 | ATGTTTGAGGAGGAC[A/G]TCAACTCGACTGGAG | 388795 |
rs115952536 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936625 | CAATTGACTATTAGT[A/G]CATGGGTTTATTTCT | 388795 |
rs116023449 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904941 | CAGAATGGAGTTTTG[A/T]AGAGTGTAGTAGAAG | 388795 |
rs116030813 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911020 | TAGGATTACAGGCGT[A/G]AGCCACTGTGCCCAG | 388795 |
rs116043038 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925190 | GATCCAGGCCCAGCT[C/G]TGTCCCTGACAGTCT | 388795 |
rs116131708 | snp | A/G | 0.02016 | 0.0983543 | missense | EFCAB8 | GRCh38.p7 | 20:32911501 | AGTGGCTGCCTGCGC[A/G]GCACAGTGAGTGTGT | 388795 |
rs116186291 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952900 | TTAAGTATATTCACA[C/T]TGTTGTGCCATAGAT | 388795 |
rs116226034 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920392 | AGTCAGGGCTGCGGT[A/G]TCTGGGGAGAGCTCC | 388795 |
rs116244843 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936723 | TATTAGCTTTATAAT[A/G]TATTTTGAAATCAGG | 388795 |
rs116277162 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909012 | TAAGGGGGCCCACAA[G/T]AAGGTGGAGGCTTGG | 388795 |
rs116277805 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902766 | CCCCAACCTCTGCCT[C/T]TGGAGTCAGCCTCAG | 388795 |
rs116317089 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886348 | TAGTAAGTGAGAAGA[C/T]GCTCAGGAGAACCCA | 388795 |
rs116368963 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870405 | TTTTTCATGATACTT[G/T]TTTGATATACAGAGA | 388795 |
rs116372875 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911164 | TTCTTATTTTTTTGA[C/T]GGGGTGGTCATGATT | 388795 |
rs116428468 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867947 | GCTCAAGCGATCCTC[C/T]TGTCTCAGCCCCCAG | 388795 |
rs116428875 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901521 | ATCAGGGGGTCACCT[C/T]ACCAGGGCCAGGAGG | 388795 |
rs116444857 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912918 | CTGCGTGTTCTCTCT[C/T]CAGATGGGTTCCTCC | 388795 |
rs116473995 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887880 | TGCAGAACAAATTAT[C/T]GGTTAGTAAGCCAAT | 388795 |
rs116533793 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919341 | GGCAGTCTAGACCTA[A/G]ATCCAACATGGTCTG | 388795 |
rs116568949 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890037 | CTCTCCTGCATGCCG[C/T]GCTTCCCTGATGCCC | 388795 |
rs116590774 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953501 | CTTGTTATTTTGTTT[C/T]TGTTTTTTTTGTTTG | 388795 |
rs116697586 | snp | A/G | 0.00533624 | 0.0513775 | missense | EFCAB8 | GRCh38.p7 | 20:32918434 | GAGCGGGAGAAGTGG[A/G]CATACAAGACCTCCA | 388795 |
rs116698038 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889696 | GTCCAGGCCCCCTTC[A/G]CTGTCACTTAAATAG | 388795 |
rs116735380 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950989 | GAAGCATGGAAAACA[A/G]TGCGCAATATTTATT | 388795 |
rs116751509 | snp | C/T | 0.0146672 | 0.084371 | missense | EFCAB8 | GRCh38.p7 | 20:32961466 | GCCCATTCCACCCCC[C/T]CGGTCCCATCCCCGG | 388795 |
rs116753585 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914601 | CAATCATAGTTAAAG[A/G]TGAAGGGGAAGCAAG | 388795 |
rs116765471 | snp | C/T | 0.483923 | 0.0882034 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892848 | TTTTTTTTTTTTTTT[C/T]TTTTTTTTATGACTC | 388795 |
rs116771121 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876261 | CCAGGGACAAGTGTC[A/G]TTGGCCCCTGTGTGA | 388795 |
rs116914782 | snp | C/G | 0.0165278 | 0.0893908 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867202 | TGGGATTATGGGCAT[C/G]AGCCACCATGCCCAG | 388795 |
rs116926098 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929768 | ATTTGCTCTACCACC[C/T]TCACTATGCTCTCAG | 388795 |
rs116944486 | snp | A/G | 0.00511554 | 0.050315 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32920209 | ATCCAGTGCCTCGGT[A/G]GAGAAGGTTGGCCGT | 388795 |
rs116976597 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883252 | TATATCCTTCAGTCG[C/T]AGGGGTAGCTTCAGT | 388795 |
rs117060085 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866244 | ACATTTGCTCTTTAG[A/T]TGGGGCTAAGTGGGG | 388795 |
rs117131321 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863379 | GGTATATGCAGTGGA[A/C]ATGAGGAGCCCTCAT | 388795 |
rs117150601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872041 | CCTTGGCTGTAACTC[C/T]AGATAAACAAGATGG | 388795 |
rs117211746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926045 | ACCGGATGCTGGCTA[C/T]GCAGTTGACCCTGTG | 388795 |
rs117268152 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897137 | TACCTGTATTCCCCC[C/T]ATCTACTTCCTGTGG | 388795 |
rs117394865 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943094 | TTCAGTAGTTTTATT[C/T]TCTCAGTGTAATGTG | 388795 |
rs117487769 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897814 | CAGATGCTTGGTGAC[A/G]GTGTGTGTAAAACCC | 388795 |
rs117534457 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885400 | TGTGCGTGACGCTCC[A/G]CCGGCTTTTGTCCCT | 388795 |
rs117554005 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909719 | TGCGTGTGGTCAGGA[C/T]GTCTTGATGTCGTGA | 388795 |
rs117680826 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897529 | CTCACTGCAGCCTTG[A/G]CCTCCCGGGCTTAGG | 388795 |
rs117688888 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909246 | TTATCTCCTTGCTGA[A/G]TGCCAGACAGGTGGT | 388795 |
rs117708335 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900555 | TATTTTTCATTTTTT[A/C]ATTTTTATTATTTTT | 388795 |
rs117765537 | snp | A/G | 0.0474399 | 0.146524 | missense | EFCAB8 | GRCh38.p7 | 20:32930423 | TGCAGACCAGGCCTC[A/G]CCTGCCGCACACGGC | 388795 |
rs117810035 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951313 | TGAGTTGATAAACTA[C/T]GGTTTATGGAATATC | 388795 |
rs117904105 | snp | C/T | 0.126219 | 0.217206 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871097 | ACCTCAGGTGATCCA[C/T]CTGTCTCGCCTCCCA | 388795 |
rs117909903 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890035 | GCCTCTCCTGCATGC[C/T]GCGCTTCCCTGATGC | 388795 |
rs117924512 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919566 | CAGTGGCGTGGTCTT[C/T]GCTCAGTGCAACCTC | 388795 |
rs117962900 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923952 | TAGGATTAGAAACAT[A/C]CTCCTGGAAAGCTTT | 388795 |
rs118071781 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865827 | TTTGCTGCCTAGAAA[A/G]ATGACTGGTGCCAGT | 388795 |
rs118072173 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953118 | TAGCATAATGCCCTC[A/C/G]ATATTTATTAATATT | 388795 |
rs118131001 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921222 | TTTTCTTGAGACAGG[A/G]TCTCACTGTCACCCA | 388795 |
rs137860663 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921882 | GTCACCCAGGCTGGC[A/G]TGCAGTGTTGCGATA | 388795 |
rs137894756 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919979 | CCTACTGCGGGGGCT[C/T]GGGAGTGCCGCTCTT | 388795 |
rs137974026 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958906 | AGGTCCCTGGCAGAG[A/G]AGTGCTCAGGCCCAG | 388795 |
rs137982231 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891275 | ATTTTGGTTGAAAAA[A/G]AAATATTGAATTCTG | 388795 |
rs138001170 | snp | A/G | 0.000822223 | 0.0202592 | missense | EFCAB8 | GRCh38.p7 | 20:32931202 | ATCAAGGATTACTGC[A/G]CATTGATTGATAAAC | 388795 |
rs138051232 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915765 | CAGCCTCCGCGTCCC[A/G]GGTTCAAGTGATTCT | 388795 |
rs138066480 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944320 | AAATACAAAAATTAG[A/C]CAGGCATGGTGGTGC | 388795 |
rs138080423 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880355 | CTCACTGCAACCTCC[A/G]CCCCCCGGGTTCAAG | 388795 |
rs138083858 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955209 | AGAGACAAGAACACA[A/G]GTGAAAAACAGAATG | 388795 |
rs138089607 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865394 | CCTGGAACATGGTGC[A/G]TGCTTGAAACTAGAA | 388795 |
rs138116494 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932056 | ATTAACGGGCCTGAT[C/G]ATGCAGTTGTATTCA | 388795 |
rs138123952 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888155 | TGCAGCCTCAACCTC[C/T]TGGGGTCAAGGGATC | 388795 |
rs138125491 | snp | A/G | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860527 | TTTTTTTTTTTTTGA[A/G]ATGGAGTCTTACTCT | 388795 |
rs138158930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943627 | TTTCTCCTGTACTGT[C/T]CCCTATAGGTTGTGG | 388795 |
rs138170887 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880154 | GTGGGTCTGTCCTAA[A/G]AGGACCAGACCCAGA | 388795 |
rs138175631 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905016 | GCACAGAGCATCTGC[A/G]GTTCTTAGGCCTGTG | 388795 |
rs138245179 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902411 | TGTTCCCTTCCTTCA[G/T]CCTGGGTGACAGAGC | 388795 |
rs138254021 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901931 | GACCTCATGATTCGC[C/G]CGCCTCGGCCTCCCA | 388795 |
rs138390793 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915569 | TTTCTCTGCATCTGT[C/T]CTCTTTTCTTTCTAG | 388795 |
rs138432736 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956154 | TATTCTTTTAGTGAT[C/T]ACCTTAGAGATTATA | 388795 |
rs138441764 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876139 | GATGGGAGGCCATCA[C/T]GATGTGGGAAAGCCT | 388795 |
rs138444512 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922393 | CAAAGCTTGATCTTT[C/T]GGGCTAGTGACCTAG | 388795 |
rs138449076 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863112 | GTCTGCCCCCTGTGC[A/G]TGTCTTGGGCTTAAC | 388795 |
rs138476599 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873477 | ATAGACCCAGCCAGC[A/C]CGTGGAGAATTTTCT | 388795 |
rs138503800 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958678 | GGAGGACCCTCAGAA[G/T]GCCAGAGGCTTGAGG | 388795 |
rs138510789 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891179 | CAGTGGCACAATCTC[A/G]GCTCACTGCAACCTC | 388795 |
rs138542119 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888219 | CAGGCATGCACCACC[A/G]TGTCCAGCTAATTTT | 388795 |
rs138605780 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884636 | AGGCCTACCGGATTT[A/G]GAAAGGGCCCTGGAG | 388795 |
rs138637860 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919687 | TATTTTTATTGGAGA[C/T]GGGGTTTCACCATGT | 388795 |
rs138642675 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890692 | GGAGAGAGAGTGGCT[-/G]GTTCTGGAACAAGCA | 388795 |
rs138647269 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894306 | GGCTTGTTGGGGCAG[C/T]GTCCCCTGCTGGCAG | 388795 |
rs138685509 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876571 | ATTGATGTAGCAAAG[A/G]TGACAATGATAACTA | 388795 |
rs138686049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865669 | CCAGGCGTGGTGACT[C/T]ATGCCTGTAGTCCCA | 388795 |
rs138713323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862423 | CCTAGTATCACATGC[A/G]TTAAAACCACTTTCC | 388795 |
rs138719958 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898221 | GATGATTAGTATGGG[C/T]CTGACCTTCCCCATC | 388795 |
rs138735745 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910529 | CTGGACAGGTGCGCC[A/G]CATCGGCTGCAGAGG | 388795 |
rs138747168 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943585 | GGTGCCTTCTAATTA[A/G]CCTGTGTAGTGGTCT | 388795 |
rs138761608 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859941 | AGAATCGTGCATTGC[C/G]TTTAGTTGTTGGGTC | 388795 |
rs138787582 | snp | A/G | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32911525 | AGTGTGTGGGAGGTC[A/G]TGACGGGCAGGAAGA | 388795 |
rs138825272 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936278 | ACCTCAGGCAATCCG[A/C]CTGACTCAGCCTCCC | 388795 |
rs138868032 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934961 | TGTACAAGGGTTTTC[C/T]TTTTTCTGCCTCCTC | 388795 |
rs138981996 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904642 | GGCGGTGGCGGGGTG[A/G]GGGTACTGAGTCTTT | 388795 |
rs139015815 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901966 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCTCCT | 388795 |
rs139017457 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873462 | CAGACAGATCCCCTT[A/G]TAGACCCAGCCAGCA | 388795 |
rs139047561 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913969 | TGGGCAGCCCTACAC[C/T]TACAGATTTGGGGAG | 388795 |
rs139048506 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884974 | CTGCCCCCGGAGCTG[C/T]TGGCTGTAGGTTTGG | 388795 |
rs139048796 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944971 | ATATTGTCCATTTGA[C/T]GATGTCTCATAAATC | 388795 |
rs139058863 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860883 | AGCTGGGACTACAGG[A/G]GAGTGTCACCATACC | 388795 |
rs139114548 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881862 | TCCACCCCCATCAGG[C/T]CCTTAGGGAATTCTG | 388795 |
rs139120506 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902751 | GGCCTGGCATTGGCA[C/T]CCCAACCTCTGCCTC | 388795 |
rs139138838 | in-del | -/AAG | 0.00478085 | 0.0486577 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917740 | TAAGGTCACACAGCC[-/AAG]AAGGAGTAGACCCAA | 388795 |
rs139142781 | snp | C/T | | | missense | EFCAB8 | GRCh38.p7 | 20:32918387 | TGAACAACTGCCTGG[C/T]TGAGAGCCACAGGCC | 388795 |
rs139145935 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884368 | TGGCCTGTCCTTAGG[G/T]CTGTCTTCCCTTTTC | 388795 |
rs139247116 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913314 | GTCTTCTTACTGTAA[A/C]CTTACATGGTGGAAG | 388795 |
rs139254776 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868614 | TGCACGTTTATCACC[C/T]CACAGTTCTGGTGGG | 388795 |
rs139362635 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951210 | ATGAAAGCATATGCC[C/T]GGGTAAAGACTACAT | 388795 |
rs139371323 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886387 | TTGGTCGCCAGGGCC[A/G]TCCAGAATCCTCCAG | 388795 |
rs139405013 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895861 | CAGGCGTGAGCCACC[A/G]TGCCTGGCCCAGGCT | 388795 |
rs139470584 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870487 | ATTACTGTTTTCTGT[C/T]TCCTGTGATCTTTAT | 388795 |
rs139528448 | in-del | -/AAGAAAAAGAGTT | 0.245346 | 0.249957 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931762 | GACTTCGTTTCAAAA[-/AAGAAAAAGAGTT]AGTATTCGTAATAAT | 388795 |
rs139546264 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867912 | GTGGTGTGATCACCA[C/T]GGCAGCCTCAACCTC | 388795 |
rs139546356 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936664 | TATCTTGTTACATTA[A/G]TCGATGTGTCTATTT | 388795 |
rs139546714 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874597 | CTCAGGCTGGAGTGC[A/G]GTGGTGCAATCTCGG | 388795 |
rs139612590 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900415 | CACCAGGCTGGAGTG[C/G]AGTGGCGCAATCTCG | 388795 |
rs139671156 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899622 | TCTTGTTGCCCAGGC[C/T]GGAGTGTAATGGTGC | 388795 |
rs139679724 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940505 | ATAAATGGAAAATAC[A/T]TGTGACCTTAGACAG | 388795 |
rs139693801 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877635 | AGGGCTTTACCCAGT[A/G]GTCCTTGTTTACAAC | 388795 |
rs139756965 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960307 | GATTCTGGGCCATGG[A/G]CAGGTCTGGGATGAG | 388795 |
rs139762068 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875028 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGTGCC | 388795 |
rs139861538 | snp | A/G | 0.01365 | 0.081478 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32885622 | GTCTGAGTCCTTCTC[A/G]CTGATGAGCTCCTTT | 388795 |
rs139892725 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916302 | TTGCTCTATTGCCTA[A/G]GCTGGAGTGCAGTGG | 388795 |
rs139895502 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897302 | CTCCTCAACGGCAGC[A/G]GCTTCGTGCTCTCGG | 388795 |
rs139897962 | snp | C/G | 0.00541355 | 0.0517443 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32917346 | CTACCACTGGCAGAC[C/G]TACCACACGGAGGAC | 388795 |
rs139899532 | in-del | -/TAT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924509 | CTGAAAAGAATGTAC[-/TAT]TATTATTATTCCCAT | 388795 |