SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs139915548 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956960 | TTTTTTTTTTTTTCA[-/T]TTTTTTTCAATCTCT | 388795 |
rs139986616 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867150 | GTCTCAAACTCCTGA[C/T]CTCAAATGATCCGCC | 388795 |
rs140068866 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932588 | TACTTATGCAAACAC[A/G]ATGTGTAAAGTTATT | 388795 |
rs140072319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870921 | TAGAGTGCAGTGGTG[C/T]GATCTCGGCTCACTG | 388795 |
rs140102524 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929650 | AGATTTTTGATAATC[G/T]AGATTTTTGTTGTTG | 388795 |
rs140110099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923206 | AACAAACAAACCTGG[C/T]CCAGTGCGATGGCTC | 388795 |
rs140112056 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863454 | AAGATTCTTCTACTT[A/C]TGTAGAAAGTGTGAT | 388795 |
rs140174849 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920483 | GTTTAACTGGACTTA[C/T]AGTTCCATATGGCTG | 388795 |
rs140236853 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938707 | AAATACTTAGGAATA[A/C]ATTTGGAAAAGTAGT | 388795 |
rs140242291 | snp | C/T | 0.00182786 | 0.0301759 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32959874 | AGATAAGGAGGCAGA[C/T]ACTTGGGCCAAGCTG | 388795 |
rs140301277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954258 | GGAGTTTTTACAGTT[C/T]TGGGTATTATCTTTA | 388795 |
rs140345370 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924923 | GCAGGGTCCCTTCTC[G/T]CTGGGGCACTTGTGG | 388795 |
rs140349148 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864822 | TAAGTTAAACATGCC[G/T]TTGTCTTTGAAGAGC | 388795 |
rs140379475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921749 | GCTATGTCCTGCCAT[A/G]TGCTTTTTTCTGTAA | 388795 |
rs140386041 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897563 | TCCTCCCACCTCAGG[C/T]CCCCGAGTAGCTGGG | 388795 |
rs140419631 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933750 | TTGGGAGGCCGAGGC[G/T]GGCAGATCACCTGAG | 388795 |
rs140451264 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915278 | TATAAGTTGTCAGGA[A/G]AAACCAGGAACTCCT | 388795 |
rs140508966 | in-del | -/TGTGTGTG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921362 | TATGCCCAGCTATTT[-/TGTGTGTG]TGTGTGTGTGTGTGT | 388795 |
rs140527644 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907575 | TAGGGGACAGGTTAC[A/G]TTTTCTGGAACTCTG | 388795 |
rs140592303 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903279 | GGGCTGACTCCTTCT[C/T]ACCCTTCAGGTCTCC | 388795 |
rs140593993 | in-del | -/TT | 0.405255 | 0.195948 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870860 | TTCTACTTCTTCTTC[-/TT]TTTTTTTTTTTTCCT | 388795 |
rs140594090 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944761 | TGGATGAGAGTTTTT[A/G]TTCTTTTTATAATGT | 388795 |
rs140605575 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864641 | CCGAGCCCCCTGATG[C/T]ACGGTCTGTACGTGG | 388795 |
rs140700864 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947052 | ATAGGACATTTGAGT[A/C]ATTGTCAGTTTTGGA | 388795 |
rs140803055 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904019 | GAATGGATTTTTTGG[G/T]TTTTTTTTTTCTGAG | 388795 |
rs140830251 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919236 | CAGTGAGATTGTTCT[C/T]GTAGTCAAAATCTGA | 388795 |
rs140872070 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930143 | TCATGTATTATGTGT[C/T]AGGCACCATTGTGGT | 388795 |
rs140873282 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868856 | TGGGCGTGGTGGCAC[A/G]GGCCTCTAATTCCAG | 388795 |
rs140941150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891312 | TGATGGGCTGGACCT[A/G]GTCTGCTGGGCCCGT | 388795 |
rs140949689 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861971 | AACCTCTTAATTGCC[C/T]TTTTCAGTGGCTGTT | 388795 |
rs140961679 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862245 | AAGTAATTCTCCCAC[C/T]TCAGCCTCCTGAGTA | 388795 |
rs141025647 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894059 | TGTTCTGCCCAGGTC[A/G]CTAGATCCCCAGAGG | 388795 |
rs141066403 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923340 | AAATACAAAAAATTA[C/G]CCAGGGGTGGCAGCA | 388795 |
rs141076174 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872320 | AGTCAGGGTGCATAA[C/G]GCACAGAGAACAATG | 388795 |
rs141118337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910259 | GTGCTAGTTGTGGGG[C/T]GCTTTCCTAGGTTCC | 388795 |
rs141143922 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903492 | CCTCGTGTCTGTGCC[C/G]CTGGTAATCCTGGCA | 388795 |
rs141189570 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926294 | GGAATGTGCTTATGA[C/T]AAAATTTAAAGCACA | 388795 |
rs141205806 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901174 | GTTTGCTTGGAGCTG[A/T]TTGCTGAGGCTATCT | 388795 |
rs141262397 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888118 | ACCCAGGCTGGAGTG[C/G]AGTGGTGCAATCACG | 388795 |
rs141356296 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942877 | ACTACTGTTTATTGA[A/G]TCATGTTTTCTGTTA | 388795 |
rs141379609 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881446 | AAGTGATCCATCCAC[G/T]TCGGCCTCCCAAAGT | 388795 |
rs141402337 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876315 | ACCCCACCTGCCACG[C/T]GGCTGTGGTGCCCAC | 388795 |
rs141451830 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874174 | CTTCTGCCCACCTCA[C/G]CCTCCCAAAGTACTG | 388795 |
rs141486408 | snp | C/T | 0.00212992 | 0.0325642 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32906868 | CTACGATGCCTTCAT[C/T]CGCCTGTGGAACCCC | 388795 |
rs141525614 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958896 | GCATGGCCAGAGGTC[C/T]CTGGCAGAGGAGTGC | 388795 |
rs141525623 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916490 | TCTTGAACTCCTGGC[C/T]TCAAACGATTTTCCT | 388795 |
rs141555632 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957734 | TTCTCTCTCTCTAAG[A/C]CAAGTCTGATTCTCA | 388795 |
rs141564710 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869893 | CTAAGCTATTCCTCT[A/G]TTTTCAGACGTTTAG | 388795 |
rs141621048 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953728 | TATGGATATTAACCT[C/T]TTATCAGGGATATGA | 388795 |
rs141625542 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887806 | CTGAGCTCCTACTGA[C/G]TGCTGGGCACCACCC | 388795 |
rs141628839 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950768 | TGAGGGTGAAGTTTA[A/G]CAGTTACCCAAGAGA | 388795 |
rs141633214 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863101 | TGGCTCAGTTGGTCT[G/T]CCCCCTGTGCGTGTC | 388795 |
rs141681949 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949174 | TATTTCTATATACTA[G/T]CAATGAACAGCCAGA | 388795 |
rs141744917 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859591 | ATATTTAGTTTTGAA[A/G]TAATTAAAAATATAT | 388795 |
rs141786896 | in-del | -/AAAC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950001 | AAGACTCTGTCTCAA[-/AAAC]AAACAAACAAAACAA | 388795 |
rs141807349 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912301 | AAAAAATTAGCCAGG[C/T]GTGGTGGTGGCTGCC | 388795 |
rs141873378 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902458 | AAAAAACAAAAGACT[A/C]CATTCAGGTCAGACA | 388795 |
rs141884943 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919745 | CTGAAATTATCTGCC[C/T]GCCTCAGCCTCCCAA | 388795 |
rs141904608 | snp | A/T | 0.00279496 | 0.0372783 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860735 | TCTGCATCTTGGTTT[A/T]TTTATTTATTTATTT | 388795 |
rs141905370 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940396 | ATTAGAAGAATGAAG[G/T]TAGACTCCTACCTCA | 388795 |
rs141962343 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940027 | CCTCCCTCCCTCCCT[C/T]CCTTCCTTCCTTCCT | 388795 |
rs141962611 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899667 | ACAACCTCTGCCTCC[C/T]GGGTTCAAGTGATTC | 388795 |
rs141965882 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897966 | TCCAGGTCACAGAGT[A/T]GGCGCCGGAGAATTC | 388795 |
rs141967893 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937793 | CTGGCTAATTTTTGT[A/G]TTTTTAGTAGAGACA | 388795 |
rs141988738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898792 | ACAGCAGCCTCTTTT[A/G]TCTCCCAATCTATAT | 388795 |
rs142006757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936380 | GTCATAGCTAAATAA[C/T]CATTGCTCAGATCAA | 388795 |
rs142024439 | in-del | -/AATGCCCCTCTAGCTGTGAACCTGTGATGCTAAC | 0.189576 | 0.242588 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913679 | ATTCATTCTGAAGCA[lengthTooLong]ACGTTATGTACTTCC | 388795 |
rs142032175 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934617 | GCTCTCATAATCCCC[A/G]GCTGTCGTGGGAGGG | 388795 |
rs142097092 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875350 | AGGGGCTGGATTTGA[C/G]GTTTGAGGGGCTGGA | 388795 |
rs142129677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909437 | AAGTGCTATGTGTTA[C/T]GGTAGAGTTGTGCTT | 388795 |
rs142132914 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886006 | GTCAGCCACTCCCAC[A/G]CTGTCCCCACGTCCT | 388795 |
rs142198932 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933453 | ATATCTACCACCTCA[C/G]TTACAATTTTTATGG | 388795 |
rs142200076 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872116 | TTCCTTGATCCAGCA[A/G]CAAATATAATAATAA | 388795 |
rs142266811 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923391 | GTCGGGAGGCAGAGG[C/G]AGGAGAATTGATTGA | 388795 |
rs142275978 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864586 | ACCCTGTCTCTAAAA[A/C]AACAAAACAAAAAAG | 388795 |
rs142291552 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902101 | TAGTAGCTAGTCCAC[A/G]TTAATATTTCTCTAA | 388795 |
rs142318116 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887197 | GAGGAATTGGTTTAC[A/G]CTCCTCCCTGCTCCT | 388795 |
rs142351416 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920720 | ATTCTGGGAGATACC[A/G]TTCAAGTTGAGATTT | 388795 |
rs142353806 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885083 | AGCACTAGAGCAGTT[A/G]CTAGAAAGTGCTGTT | 388795 |
rs142356080 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921916 | GCTCACTGCACCTCT[A/G]CGTCCTGAGTTCAAG | 388795 |
rs142403377 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920390 | GGAGTCAGGGCTGCG[G/T]TGTCTGGGGAGAGCT | 388795 |
rs142411460 | snp | A/G | 0.00158767 | 0.0281303 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32918502 | TACCAACCTGAGGCG[A/G]AGCCTGGTGTCGGCT | 388795 |
rs142419472 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920025 | GGTCTCTGGTCCCCT[A/G]TGGGGAAGGGAAACA | 388795 |
rs142542454 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903551 | TCAATACGTGAAATC[A/G]GCCTGAAATAATTTC | 388795 |
rs142575550 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942490 | CTAACAGTTCGAGAC[C/T]AGCCTGGGCAACATA | 388795 |
rs142615410 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868691 | ACAAGGCTGCAATCA[A/C/G]GTTGTTGGCTGGGAC | 388795 |
rs142705586 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888173 | GGGTCAAGGGATCTT[C/T]CCACCTCAGCCTCCC | 388795 |
rs142721201 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861189 | CTTTTGGTTTTTGCT[C/G]CTATGAATGATGCTG | 388795 |
rs142772292 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863271 | CTTGCTGACCCAATA[A/G]AAACGTTCTCTTTAT | 388795 |
rs142772772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898428 | GCACCTGGTCATGTT[C/T]TGGGGGCTGGGCCTA | 388795 |
rs142803859 | in-del | -/AAAC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950002 | AGACTCTGTCTCAAA[-/AAAC]AACAAACAAAACAAC | 388795 |
rs142806963 | snp | C/T | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32911529 | TGTGGGAGGTCGTGA[C/T]GGGCAGGAAGACGAT | 388795 |
rs142917658 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956276 | TATGTCTTCCTATAA[G/T]ACATTGTCATTATTA | 388795 |
rs142925643 | snp | A/C | 0.0391387 | 0.134304 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889535 | AGGATAGCCAGGTGG[A/C]GAGGCCTTAGTGCCA | 388795 |
rs143021059 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865524 | GCCTAGAAGCCAGGC[A/G]CAGTGGCCCATATCT | 388795 |
rs143097119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935868 | TGAGTTTCTTATTTA[C/T]TGTGGATGTTACTCC | 388795 |
rs143102315 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873478 | TAGACCCAGCCAGCA[A/C]GTGGAGAATTTTCTA | 388795 |
rs143151947 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884376 | CCTTAGGGCTGTCTT[C/T]CCTTTTCCTAGCTGT | 388795 |
rs143223531 | in-del | -/TGCTGTGGCC | 0.0569829 | 0.158885 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890242 | GTCTCCTCTGGTAGG[-/TGCTGTGGCC]TGGGTCTCTGTGCTC | 388795 |
rs143225006 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912601 | TGCCTACCCTATCTC[A/G]CTCCCCTAAGTCCAT | 388795 |
rs143275613 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959084 | TAATTCTGGTTCATT[C/G]AAGAAAATGTGTATT | 388795 |
rs143293637 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944235 | ATCCCAACACTTTTT[C/T]GTCCCCTTTTCCTCC | 388795 |
rs143337882 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869570 | AACAAATCATGTAAT[C/T]ATGTGCACATAGTCC | 388795 |
rs143369873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901961 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCG | 388795 |
rs143375389 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897346 | CTAAAATAGTACCCT[C/G]CGCTTGGTGGGCTCC | 388795 |
rs143404186 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914255 | GATGGTAGAGTGCTG[C/T]GGTCCCATGGGCACT | 388795 |
rs143441798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894498 | AGCCACATGGTGAAT[A/G]GGATATTGAGAGAGG | 388795 |
rs143490983 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894703 | AGTTCCCTTATTCAA[A/G]TAGGGATGGCCCTAC | 388795 |
rs143544209 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957829 | TCTTGGAAAGACTTG[C/T]CCCTTTCTGTCATCT | 388795 |
rs143557902 | snp | C/T | 9.49352e-05 | 0.00688902 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32931249 | TGGGGCCAAGGTTGT[C/T]TCTGAAGCACACAAC | 388795 |
rs143566425 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916552 | GCATGAGCCACCATG[A/C]CTAGCCTAGGACCTC | 388795 |
rs143618489 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862805 | GCTAATTTTTTATAT[A/T]TTTAGTAGAGACAGG | 388795 |
rs143640532 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880371 | CCCCCCGGGTTCAAG[C/T]GATTCTCCCGCCTCA | 388795 |
rs143660912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897275 | ATGCTGTCACCTTCA[C/T]GAGATCGACAGCTCC | 388795 |
rs143688150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940828 | ATGATGGTGAACATC[A/G]TTAGCTATCAGGGAA | 388795 |
rs143721444 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887854 | ATTATTCCATTCATT[A/C/T]CTCGCAACTTTGCAG | 388795 |
rs143727998 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932665 | TTCTTGCTGTATGAT[A/G]TATCTTGGAGACCTT | 388795 |
rs143754678 | snp | A/G | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32898568 | TCCTGTTCAGCCATC[A/G]AGAAGTCCTCTCTGG | 388795 |
rs143789503 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935478 | GTGCTGGGATTACAG[A/G]CATGAGCCACTGCAC | 388795 |
rs143790920 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946048 | TTGGATATGTATGCT[C/T]CAAATCTGCCTCCTC | 388795 |
rs143825737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947901 | CAAGACCCCATCTCA[A/G]TTAAAAAAAAAAAAA | 388795 |
rs143903842 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880188 | GGCCACGGGGAAGTC[A/C]AAGAGCTGGAAGGCA | 388795 |
rs143908936 | in-del | -/TAGT | 0.0134861 | 0.0810011 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867263 | AGATTTGAAATGATA[-/TAGT]TACTGAACTGAGGTC | 388795 |
rs143935165 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915759 | TCACTGCAGCCTCCG[C/T]GTCCCGGGTTCAAGT | 388795 |
rs143956878 | snp | C/G | 0.000276383 | 0.0117522 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920049 | GGAAACACCCTCATG[C/G]TGACTTGGGTGCCCA | 388795 |
rs143998353 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927405 | GCTGGAGTGCAGTGA[C/T]GTGATCTTGGTTCAC | 388795 |
rs144004511 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866357 | TCAGTGAGCAGGACT[A/G]CCTGCCTGCCACTCA | 388795 |
rs144022542 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882340 | ACCCAGCATTTCCTC[A/G/T]TTGGTCACTTGATAG | 388795 |
rs144059142 | snp | A/G | 0.000182149 | 0.00954157 | missense | EFCAB8 | GRCh38.p7 | 20:32878727 | TGTGGATTACATGAT[A/G]CGTGAGTTCCAGGGA | 388795 |
rs144059860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923248 | CCTAGCACTTTGGGA[A/G]GCTGAGGTGGGCAGA | 388795 |
rs144079386 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903114 | TATGGAGCCTTCAAC[A/G]GCTCCTGGCCAGGGC | 388795 |
rs144085454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881292 | ACCTCTGCCTCCCGG[A/G]TTCAAGTGATTCTTC | 388795 |
rs144092733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929657 | TGATAATCGAGATTT[C/T]TGTTGTTGGTGACAT | 388795 |
rs144162232 | snp | C/T | 0.039522 | 0.134904 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915917 | GCCTCAAGTGATCCA[C/T]CTGTCTCAGTTCCCA | 388795 |
rs144222478 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896152 | CTCCCTAATGAAGAA[C/T]TAGCTTGTTTAGATT | 388795 |
rs144256734 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938093 | ATTGAAACCAACAAC[A/T]TATGAAAATGATTAT | 388795 |
rs144264221 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867921 | TCACCACGGCAGCCT[C/T]AACCTCCCATGCTCA | 388795 |
rs144333107 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864756 | ATCAATTGTCTGTTA[C/T]GTGCTTGGGGCTGGG | 388795 |
rs144333157 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900615 | CTGTGTTGCCAAGCT[A/G]GAGTGCAGTGGCACA | 388795 |
rs144388952 | snp | C/G/T | 0.00478244 | 0.0486902 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913499 | CAGTCTATGGCATTC[C/G/T]GTCCCTGACTTCCCA | 388795 |
rs144400554 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863570 | AGGGGAAGAAAGGCT[C/G]AAGTGCAAGCTTGGC | 388795 |
rs144417191 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874691 | GGATTACAGGCACAC[A/G]CCACCAAACATGGCT | 388795 |
rs144481915 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907695 | GCCCTGGGAGCTGGG[A/T]TCATCGCCTCTGATG | 388795 |
rs144544148 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903323 | CTCCTCAGAGAGGCC[A/G]GCAGAAGTGAGCCTC | 388795 |
rs144662166 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928396 | GCATGCCACCACACC[C/T]GGCTAATATTTGTAT | 388795 |
rs144670167 | snp | C/T | 0.000920641 | 0.0214353 | missense | EFCAB8 | GRCh38.p7 | 20:32867658 | CCCTTAGCCAGGTGC[C/T]TGACCTCCAGCCTGG | 388795 |
rs144708348 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877079 | TCATCAGCACTGGAG[C/T]CAGTATTCAAACCAG | 388795 |
rs144773845 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862365 | ACTCCTGGATGCAAG[C/T]GATCCTCCCGCCTCG | 388795 |
rs144825650 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861366 | CAATCTCGGCTCACC[A/G]CAACCTCCGCCTCCT | 388795 |
rs144826531 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32961047 | GGGAAGACCTCAGGG[C/T]GCCTCCTTCCTGTGA | 388795 |
rs144843134 | snp | A/G | 0.0248432 | 0.108648 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859763 | TACTTTTCAGTGTAC[A/G]TTTCCTGAAACAAGG | 388795 |
rs144874051 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897591 | GGGAATACAAGCACC[A/C]CACCCAGCTAATTTT | 388795 |
rs144888271 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891333 | CTGGGCCCGTGTTTG[C/T]TGGCTCATCAGGTGT | 388795 |
rs144889337 | snp | C/G | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32958490 | GTGAAAACAGAGCAA[C/G]CTTAGAGGAAGATGG | 388795 |
rs144909370 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891178 | GCAGTGGCACAATCT[C/T]GGCTCACTGCAACCT | 388795 |
rs144915387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908595 | AAATCCTGTTTCTAG[A/G]CCCCCAGCCTGTCAC | 388795 |
rs144946987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957171 | ATTTTCCTTAATTTT[A/G]TTTAACATTATTTGT | 388795 |
rs144977934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960891 | GCAGTCTGCTCGCCA[A/G]CTCACAGAGTTGCCA | 388795 |
rs144988001 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871105 | TGATCCACCTGTCTC[A/G]CCTCCCAAAGTTCTG | 388795 |
rs145171298 | snp | C/T | 0.039522 | 0.134904 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939804 | GATTCAAGCGATTCT[C/T]CTGCCTCAGCCTCCC | 388795 |
rs145173065 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876542 | ACAGAAAAGTACCAA[A/G]GATAGTCTGACAAAT | 388795 |
rs145247957 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889986 | AGCATGGGCGACAGA[A/G]AGAGACTCAGTCTTA | 388795 |
rs145282025 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877888 | AGTTGTGGGGGTGAT[C/G]TGAGGATGCACTTAG | 388795 |
rs145286611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958898 | ATGGCCAGAGGTCCC[C/T]GGCAGAGGAGTGCTC | 388795 |
rs145307302 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937640 | TTTTTTTTTGTTGAG[A/G]CAGAGTCTCACTCTA | 388795 |
rs145316370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875140 | TCTTTTTTAGTGCCT[C/T]CCCTCCCCACACTGC | 388795 |
rs145345123 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917969 | GGTTTTCCAAATGTA[C/G]TGGAGAGAGATGCTT | 388795 |
rs145401939 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957781 | ACTCAGGAGTGCCCC[C/T]GAGACAAGAAAGCAG | 388795 |
rs145404919 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951739 | AATTTGCATTCCTCT[A/T]GTGACTAATGATGTT | 388795 |
rs145441030 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890926 | TTAATCAACACTGAC[A/G]TCATTATGAGGCTAA | 388795 |
rs145443519 | snp | A/G | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32930606 | CGGGGGATTGTAAAG[A/G]ATACATCAAGGTGAG | 388795 |
rs145478289 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942157 | GGTCTATCAGAGTGT[A/C]TTTCTTATAGAAGGC | 388795 |
rs145509161 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925333 | CAAGTGATTCTCGTG[C/T]CTCAACCTCCTGAGT | 388795 |
rs145550080 | snp | C/T | 0.040671 | 0.13668 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900654 | TCACTGCAACCTCCG[C/T]CTCTCGGGTTCAAGC | 388795 |
rs145629173 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863509 | AAGTCAGGAGTAAAG[A/G]AACTTGTGAAACCCC | 388795 |
rs145694096 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920605 | TGATAAACCCATCAG[A/G]TCTCGCTGAGACTTG | 388795 |
rs145758773 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920928 | AAGGGTGTTTTATAC[C/T]GAACACGAGTTGGGT | 388795 |
rs145785114 | snp | C/G | 0.00953873 | 0.0683987 | | | GRCh38.p7 | 20:32875660 | CAGGTACCCACCACT[C/G]TGCCCAGCCAATTTA | 388795 |
rs145823473 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898009 | GCCCCTTCGACTGCG[C/T]GTCATCTTTTGTGGT | 388795 |
rs145836123 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882944 | TCATGATCTGCCCGC[A/C]TCGGCCTCCCAAAGT | 388795 |
rs145848845 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910141 | GCTCAGAGCTCCATC[C/T]GTTAGCCATGGGATC | 388795 |
rs145868532 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917718 | CACGGAGATGAAGCA[C/T]CTTGCCTAAGGTCAC | 388795 |
rs145879623 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875072 | CTTTTCTTTGGAGAG[-/T]TTTTCTTTGTCTCAA | 388795 |
rs145886440 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934642 | GGAGGGACCTGGTGG[A/G]AGGTAATTGAATCGT | 388795 |
rs145902954 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904869 | TGACCTCAGGTGATC[C/T]GGCCGCCTTGGTCTC | 388795 |
rs145933808 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955610 | GTATTCGAGAGTCCT[A/G]TTTGGATTAGTAAAT | 388795 |
rs145935812 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888189 | CCACCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 388795 |
rs145952258 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950863 | TGTAGTTAGAAGAGA[C/T]GTGATTTCCTTGAAA | 388795 |
rs145953307 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885296 | AGCTTCTACGTGGGG[C/G]CCTTTTTCTTTTGGC | 388795 |
rs145991510 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933034 | TATTTACTGCTTGCA[A/G]TGTTCCAGGGATGGT | 388795 |
rs146055258 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873708 | TCTCTACTAAAAATA[C/G]AAAAATTAGCAGGAA | 388795 |
rs146074132 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932543 | CTGAAGTAACCACGT[A/G]TGTTGATTTTTGGTT | 388795 |
rs146075606 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870886 | TTTCCTGAAATGGAG[G/T]CTCACTCTGTCACCC | 388795 |
rs146176232 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919824 | TTTTTAACCAGGATG[G/T]TCTCTTCCAGGACAA | 388795 |
rs146180277 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860759 | TTTATTTTTTTGAGA[C/T]AAGGTCTCATTCTCT | 388795 |
rs146193708 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916661 | TACTCTCACATTGAG[A/G]ATTAGGTTTTAACAT | 388795 |
rs146213316 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956114 | TGTTTTATGTCCTCT[A/G]CTCTTTAAATGGTAT | 388795 |
rs146247714 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943822 | ATGGGTCCTGCTGAA[A/G]CTCAGCCATGCCCAT | 388795 |
rs146297676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902386 | TTACACACACAAACA[C/T]AGAGACACATGTTCC | 388795 |
rs146336087 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936550 | CCAATTTTCCTAGTA[C/T]AGTTTATTGAAAAGA | 388795 |
rs146351609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951091 | GAAACTCTCCTGCAC[A/G]GCTAATGGGAATATA | 388795 |
rs146356976 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887262 | TTTCTTCAGTTCAGA[A/G]CCTGTGGTGTCATTC | 388795 |
rs146398235 | in-del | -/C | 0.122064 | 0.214785 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957331 | ATTAAAAAAAAAAAA[-/C]CCAAAACTTTTCTGG | 388795 |
rs146471590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884072 | CCATTTAGATCTCAA[A/G]GGTGTTTAAAGGTCC | 388795 |
rs146478562 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893548 | AGGCTGTGCGGGTGC[A/G]GTCTGGGGGTGCAGG | 388795 |
rs146497319 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930115 | AAGCCTTCATTTGAT[A/G]AACATTTATTGATCA | 388795 |
rs146516311 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925572 | TGTCCAGGCTTGTCT[C/T]GAACTCCTGGCCTCA | 388795 |
rs146578028 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929470 | CCCTTCCCTCCCCTC[C/T]CCTCCCCTCCCCTCC | 388795 |
rs146579970 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868299 | ACTCCTGGGCTCAAG[C/T]AGCGCCTTCTGCCTT | 388795 |
rs146600854 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918626 | TCTCTAGCCGCCGGC[A/G]TTCACACACCGTCTG | 388795 |
rs146617002 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913663 | TGAGTCTCAAGCTAC[A/G]ATTCATTCTGAAGCA | 388795 |
rs146655712 | in-del | -/TTACA | 0.0123036 | 0.0774623 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876423 | GCCAGCCTGTGGCTG[-/TTACA]TCTAAAAGTGTCAGG | 388795 |
rs146695734 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913243 | GGGAAGTTCCAGACA[A/G]GGTGCCAGCAGATTT | 388795 |
rs146714108 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931496 | AGTCGTGGTGGCCCA[C/T]GCCTGTAATCCCAGC | 388795 |
rs146719774 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864781 | GCTGGGGAGTATAGA[A/G]ATAATTAATACAAAT | 388795 |
rs146753359 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | EFCAB8 | GRCh38.p7 | 20:32961882 | CCCTTAGGTCCTTCC[G/T]TTTCTGAGACCAGTC | 388795 |
rs146773130 | in-del | -/TG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924820 | TGTGGCTGGCAGGGC[-/TG]TGTGTGTGTGTGTGT | 388795 |
rs146781336 | in-del | -/AGG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884795 | TTGGGCAGATCAAGT[-/AGG]AGAGTGTGTGCCATG | 388795 |
rs146819549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897298 | ACAGCTCCTCAACGG[C/T]AGCGGCTTCGTGCTC | 388795 |
rs146839281 | snp | C/T | 0.00597247 | 0.0543191 | missense | EFCAB8 | GRCh38.p7 | 20:32909923 | CTCTACAGCAAGATC[C/T]TTAAGCAGGTGAGTG | 388795 |
rs146858841 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946327 | CTTCCCAATCTGCTT[C/T]ACTGAGCCAGGAGGA | 388795 |
rs146945636 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930989 | CCTTCCTGCCTGCTA[A/T]TCCAGGAGTATGGCC | 388795 |
rs146947174 | snp | C/G/T | 0.0341408 | 0.126114 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869461 | GGCTGGTCTCGAGCT[C/G/T]CCGACCTCAGGTGAT | 388795 |
rs147050457 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915288 | CAGGAGAAACCAGGA[A/C]CTCCTTCAATATGTT | 388795 |
rs147066536 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953861 | TGTTACCCAGGCTGG[A/G]GTGCAATGGTGCCAT | 388795 |
rs147066638 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910780 | GGGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 388795 |
rs147186752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907077 | TGACCTCCCTGCCCA[C/T]GGCCCCACATCTGGC | 388795 |
rs147203216 | snp | A/G/T | 0.00398755 | 0.0445055 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944501 | TAAAGTGACTTATGT[A/G/T]CCACTATTACAGTAT | 388795 |
rs147219554 | snp | C/T | 0.0711525 | 0.174681 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941144 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 388795 |
rs147276343 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910727 | TGGTCTGAAACCACC[-/C]TCACTTGCTACTTTT | 388795 |
rs147278342 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880202 | CAAAGAGCTGGAAGG[C/T]AGCCCCGGTCCTCAG | 388795 |
rs147292754 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891300 | ATTCTGGTTCGATGA[G/T]GGGCTGGACCTGGTC | 388795 |
rs147311977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889548 | GGAGAGGCCTTAGTG[C/T]CAAGTAGGCAGGGGG | 388795 |
rs147383745 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865929 | AGACTACAGTTTGGG[A/G]CGAGCAGGGGTGTGG | 388795 |
rs147412372 | in-del | -/CAAA | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950009 | GTCTCAAAAACAAAC[-/CAAA]AAAACAACAAAACAA | 388795 |
rs147417435 | snp | C/G | 0.00349456 | 0.0416542 | missense | EFCAB8 | GRCh38.p7 | 20:32911696 | ACCTTTCCCAGTCCG[C/G]AACAGCTGGAGGTCA | 388795 |
rs147417718 | snp | G/T | 0.0448719 | 0.142907 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874976 | CTGGTCTCGAACTCC[G/T]AGCCTCAGGTGATCT | 388795 |
rs147428866 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910892 | CAGGCATGCACCACC[-/C]ACCCCCAGCTAATTT | 388795 |
rs147433971 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908202 | TGTTCGCCGGAGGCA[C/T]CCCCGAGGCTTCAGG | 388795 |
rs147496701 | in-del | -/CTTC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866725 | ATTCCCTGGGGTTTT[-/CTTC]CTTCCTTCCTTCCTT | 388795 |
rs147503191 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950650 | CATCTTTCTGCAGCT[A/G]CAGGCAAATCCCCCG | 388795 |
rs147505474 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863275 | CTGACCCAATAGAAA[C/T]GTTCTCTTTATATTC | 388795 |
rs147537337 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959566 | GACAGAGTGGTGGGA[A/G]AGTGGCAGGACTGCT | 388795 |
rs147538702 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891547 | AGAGATAATTATGTC[A/G]TCACTGCTGTCCTGA | 388795 |
rs147552740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937670 | ATTGCCCAGGCTGGA[A/G]TACAATGGTGTGATC | 388795 |
rs147556833 | snp | A/C/G/T | 0.0174242 | 0.0917521 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875207 | TCAGCCAGGACTTGT[A/C/G/T]GGGTGGTTGAATGTT | 388795 |
rs147559483 | snp | A/C | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860313 | TCTCAAAAATAAAAG[A/C]AAAAAAAAACCCAGT | 388795 |
rs147568971 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933971 | AACAAAGTGAGACTC[C/T]GTCTCAAAAAATCAA | 388795 |
rs147573776 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872440 | GGGCAACAGGCTCAT[A/G]CCTGCCATCCCAGAG | 388795 |
rs147660958 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920648 | AGAATGGCATGGGAA[A/G]GACCAGCCCCCATGA | 388795 |
rs147666599 | in-del | -/TCCC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939015 | CCCTCCTTCCCTCCT[-/TCCC]TCCCTCCCTCCCTCC | 388795 |
rs147677028 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918065 | TTTTATGCTTTGGAG[C/T]TTCCATTGAGATTAA | 388795 |
rs147763627 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869092 | AATTCAGTTCCTTGC[C/T]CCTGTGTGACTGAGG | 388795 |
rs147764395 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903368 | CGTCAAAGCCATGTG[C/G]TTATGTCCCTTGCAG | 388795 |
rs147780338 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901130 | TTCAGTCTTGGGTTC[A/G]GTGCTTTGAATGGGG | 388795 |
rs147853349 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872253 | TACCAGCTGTGTGAC[A/C]TTGGGCAAGCAACCA | 388795 |
rs147867669 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957542 | TGTGTCTGTTTCAGG[C/T]TCCTCCTTCAGTGGG | 388795 |
rs147869083 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889915 | GCTGAGGCAGGAGAA[C/T]CGCTTGAACCTGGAG | 388795 |
rs147884253 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952982 | ACTCCTCCATTTCCC[A/G]TTACCTCCAGCCCCT | 388795 |
rs147885657 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887449 | GGCGTAGTGGCGCAC[A/C]CCTGTAATCCCAGCT | 388795 |
rs147971723 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862919 | ATTACAGGTATGAGC[C/T]ACTGCACCTGGCCAC | 388795 |
rs147988325 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894583 | AGGGACAAACATGAC[A/G]ATGAGGTGGGCCCAG | 388795 |
rs148025581 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918916 | AGTCCTCAAGGGCAA[G/T]TCACCTGACCTTGGC | 388795 |
rs148027426 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859543 | ACATACATAGAACCA[C/T]TTTCTCCTGGTGAAA | 388795 |
rs148113309 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877203 | TGTTTTTATTTATTT[A/C]TTTCTTTTTTTTTTT | 388795 |
rs148148065 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898768 | TGCCAGCAGCAGCAC[A/G]GTGAGAACACAGCAG | 388795 |
rs148164305 | snp | A/G | 0.16028 | 0.233346 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935742 | AACTCCTGACCTCAG[A/G]TGATCTGCCCACCTT | 388795 |
rs148201416 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926073 | GTGCTCTCAGCAGGC[C/T]GCCCCTCTCCAGTCC | 388795 |
rs148236706 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887894 | TCGGTTAGTAAGCCA[A/C]TTTGACCAGGTGACA | 388795 |
rs148253453 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921591 | AATAAAAAAGGAAGT[A/G]TATGTAAATGAAAAA | 388795 |
rs148322444 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905874 | GGAAGGCAAGCGTGG[C/T]CCTCCTGCTGCTTCT | 388795 |
rs148356022 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931614 | ATACAAAAATTAGCC[A/G]AGTGTGGTGGTGCAC | 388795 |
rs148359942 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869582 | AATCATGTGCACATA[G/T]TCCTGCACACCCTGT | 388795 |
rs148377080 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879633 | TAGGTTCAATGGAGG[A/G]TGGAAAGCTGTGGAA | 388795 |
rs148423648 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942273 | GCCTTTGTTTATTAG[C/T]GATGTTGACATATTT | 388795 |
rs148441030 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956223 | TTACATCCCTCCCAT[A/G]TTTATGTTATTATTA | 388795 |
rs148478000 | in-del | -/AAC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950020 | AAACAACAAAACAAC[-/AAC]AACAACAACAAAAAT | 388795 |
rs148480053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912069 | TATTATAGGGCCAGT[C/T]CATGGGAGTGGCATA | 388795 |
rs148591893 | in-del | -/TTGGAA | 0.0463947 | 0.145069 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909577 | AAAGGGACCTTGGAC[-/TTGGAA]TTGGAATTTGGGGTT | 388795 |
rs148598850 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916032 | GTTACAATAACACCC[C/T]ACTCCTGGTACCAGT | 388795 |
rs148669052 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933236 | GTTCCTGACCATCTG[C/T]TCTTAGTTTTATAAT | 388795 |
rs148669699 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871705 | TCTTTTAAGGAGGTG[C/G]ATTATGAGTGCGGGC | 388795 |
rs148687980 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881369 | GCCTAGCTAATTTCT[A/G]TGTTTTTAGTAGAGA | 388795 |
rs148706968 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864530 | GAGGCTACAGTCAGC[C/T]ATGATCTCGCCATTG | 388795 |
rs148723271 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896901 | GGTAGCTTCTCATCA[C/T]ATTTGGAACAAAATC | 388795 |
rs148724026 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873982 | CTGGAGTGCAGTGGT[G/T]AAATCTCTGCTCACT | 388795 |
rs148758185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920273 | TGGGCGGTCAGGATT[A/G]GGTGGTCAGGATGGG | 388795 |
rs148774664 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959061 | TTTATTCCTGACCAA[A/G]TCTCCAGTAATTCTG | 388795 |
rs148811292 | in-del | -/AT/TA | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880899 | ACATATATATATATA[-/AT/TA]AAACACCACAGGCCC | 388795 |
rs148890603 | in-del | -/AGTCATATGCA | 0.0402882 | 0.136092 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943345 | CTTGGTAAACAATGT[-/AGTCATATGCA]AGTCATATGCAAGTC | 388795 |
rs148915773 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894413 | TGCCCTGAGCTGCCC[A/C]CTTAGCTGCTTGAGC | 388795 |
rs148981485 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935098 | ATTTTTTTTCTTGAA[C/T]CTGTTGGCCATTTGA | 388795 |
rs149003729 | snp | C/G/T | 0.0268735 | 0.11332 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882974 | TGCTGGGATTACAAG[C/G/T]GTAAGCCACCGCGCC | 388795 |
rs149038988 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875208 | CAGCCAGGACTTGTG[C/G]GGTGGTTGAATGTTG | 388795 |
rs149089992 | in-del | -/G | 0.0966517 | 0.197444 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895673 | GCCTTTCGGGTTCAA[-/G]TGATTCTCCCGCCTC | 388795 |
rs149122734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925858 | TGGGCTGAGTGAGAC[C/T]GAAATGCTCACCTTC | 388795 |
rs149124245 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865454 | TTGAATGCTACACTC[C/T]GGAGTTGGGGTGAAG | 388795 |
rs149159979 | snp | C/T | 0.000121131 | 0.00778145 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859038 | GGTGAAAGTTGCTCT[C/T]CAAAAGATTGGATAC | 388795 |
rs149176291 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957824 | GCTCTTCTTGGAAAG[A/T]CTTGTCCCTTTCTGT | 388795 |
rs149176865 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890488 | ATGTCTCCTCCTCCA[C/G]ACTGGAAGGTCAGGG | 388795 |
rs149212468 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913905 | CCTGCTGGGGTGGCA[A/G]TTCTGCCCCTGCAGC | 388795 |
rs149239191 | in-del | -/T | 0.0197687 | 0.0974348 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862488 | TTTCTGTTAGCTTGC[-/T]TCTTGGCTTCCAAAT | 388795 |
rs149264704 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888414 | TATTTTTAGTACAGA[C/T]GGGGTTTCAACATTG | 388795 |
rs149280550 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922561 | GGGCATGTCACAGAG[G/T]GAGTGAGGACAATGG | 388795 |
rs149315082 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950116 | GAAAACCTTTGTGAC[C/T]TTGGTTTAGGCAAAG | 388795 |
rs149316544 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884657 | GGCCCTGGAGGAGGG[A/G]TCACAGTGCCTAGGT | 388795 |
rs149352571 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876642 | TTTTACTTAAACCTC[A/G]TAGGAATCCTATGGG | 388795 |
rs149408469 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872949 | ATACAAAAATTAGCC[A/G]AGTGTGATGGTGGGC | 388795 |
rs149476405 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861105 | AGTCAGATTCATCCT[A/T]CTGATGTTTGGGTGA | 388795 |
rs149491080 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958987 | AGGGAGGAGCAGGCT[G/T]CTGGCTACTTGGTCC | 388795 |
rs149495008 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891278 | TTGGTTGAAAAAAAA[A/G]TATTGAATTCTGGTT | 388795 |
rs149497070 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869538 | GCTGTGCCTGGCCAG[G/T]TGTTGCAATCTTATA | 388795 |
rs149529555 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915879 | GGTTTCATCATGTTG[A/G]CCAGGCTGGTCTTGA | 388795 |
rs149546149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955371 | AATGTGAGACCCTGT[C/T]TCTACAAAAAATTAA | 388795 |
rs149579127 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32943791 | GGCTTGGAAACTCTC[C/T]GGTGATGCCATTGGT | 388795 |
rs149649054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895928 | CTGAGCCTCCTAAAG[C/T]GCTGGGATTACAGGT | 388795 |
rs149788251 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920747 | ATTTGAGTGGGGACA[C/G]AGCCAAACCATATCA | 388795 |
rs149789806 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862082 | CTAAATGTAGCCACT[C/T]CTCAAGTTTCAGTCC | 388795 |
rs149805049 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960700 | GAATATTGTGGGAGC[G/T]CCCTCCTCCCTGTGG | 388795 |
rs149824735 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882669 | GGGATTACAGGTGGC[C/T]GCCACCACGCCTGGC | 388795 |
rs149841158 | snp | A/G | 8.86486e-05 | 0.00665706 | missense | EFCAB8 | GRCh38.p7 | 20:32917440 | CTCTTCTGGAACACC[A/G]GCACACTCAAGCCCA | 388795 |
rs149862819 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867172 | TGATCCGCCCTCCTC[A/G]GCCTCCCGAAGTGCT | 388795 |
rs149998245 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889955 | GCAGTAAGCTGAGAT[C/T]GCGCCATTGCACTCC | 388795 |
rs150015245 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923936 | TCCAGATATAAAACT[C/G/T]TAGGATTAGAAACAT | 388795 |
rs150049167 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951429 | GACGAAAACCTGTAC[A/T]TATTGTATGATTCTA | 388795 |
rs150052865 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886581 | TGGGGTCCCATGGCT[C/G]TCCTTGGTGCACCAA | 388795 |
rs150121624 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872857 | AGCATTTTGGGAGGC[C/T]GAGGTGGGCGGATCG | 388795 |
rs150136204 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884630 | CAGACCAGGCCTACC[A/G]GATTTGGAAAGGGCC | 388795 |
rs150137986 | in-del | -/CCTT | 0.122411 | 0.214991 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938984 | TCTTTCTTTTCCTTC[-/CCTT]CCTTCCTTCCTTCCC | 388795 |
rs150152457 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919640 | TAGCTGGGATTACAG[A/G]TGTGCACAACTATGC | 388795 |
rs150173350 | snp | A/G | 0.00104284 | 0.0228108 | missense | EFCAB8 | GRCh38.p7 | 20:32930534 | CTGTGGACCTAGACA[A/G]TGGGGATGTTGTCGT | 388795 |
rs150173636 | snp | A/G | 0.029116 | 0.117091 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868921 | ATCTGGGAAGCAGAG[A/G]TTGCAGTGAGCCAAG | 388795 |
rs150189067 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910427 | TGGGCATGAGGAGTT[A/G/T]CTTCTGAGGTGTGAG | 388795 |
rs150204931 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948973 | ATTCAAAATTATACT[A/G]GAAGAGTAGAGGGCA | 388795 |
rs150243433 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904056 | TGTCGTTCTGTTGCC[C/T]AGGCTGGAGCTCACT | 388795 |
rs150322386 | in-del | -/TC | 0.244205 | 0.249933 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922813 | TCGAGAATGAGTACT[-/TC]TTCTCTCTCTCTCTC | 388795 |
rs150362702 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955035 | TGAGTAGAGTGGCCA[A/G]TGGGAATTCAAAATA | 388795 |
rs150363337 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888148 | GGCTCACTGCAGCCT[C/T]AACCTCCTGGGGTCA | 388795 |
rs150365248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865254 | AGGTTCCATTTGAGC[A/G]AGAGTCTGAAGAGTG | 388795 |
rs150381653 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897568 | CCACCTCAGGCCCCC[A/G]AGTAGCTGGGAATAC | 388795 |
rs150400786 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879955 | TCCCCCTGGACTCCC[C/T]AAGCATGAGGAGCAT | 388795 |
rs150450736 | in-del | -/TG | 0.0452528 | 0.143452 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959230 | GGCTGCAATTTTATG[-/TG]ATAAGTAATGAGAGT | 388795 |
rs150504280 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912398 | GATCCCGCCATCGCA[C/T]TCCAGCCTGGGCAGC | 388795 |
rs150522480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921918 | TCACTGCACCTCTGC[A/G]TCCTGAGTTCAAGTG | 388795 |
rs150523745 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863111 | GGTCTGCCCCCTGTG[C/G]GTGTCTTGGGCTTAA | 388795 |
rs150593336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877918 | GCGCCTCAGGACGGC[A/G]AGGGAGACGCTGCTG | 388795 |
rs150642913 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902729 | AGGGCATATCCTCTG[C/T]GGGTGGGGCCTGGCA | 388795 |
rs150659516 | snp | A/G | 0.00549267 | 0.0521169 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32917319 | CCACAAGACCAAGCC[A/G]GTGCTCTTGTGCTAC | 388795 |
rs150666666 | in-del | -/C | 0.0399052 | 0.1355 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955984 | ATCAACAATTATGTA[-/C]GTTGGGTTGAAGTCA | 388795 |
rs150675702 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956464 | AGATTAATAATTTTC[A/T]GATCAAATTTTCTGA | 388795 |
rs150681576 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866934 | TTCTTTCGTTTCTTT[G/T]TTTTTTGAAGTCTTG | 388795 |
rs150697115 | snp | C/G/T | 0.0111351 | 0.0739376 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899107 | AAACTAGTTAGTCAC[C/G/T]GGGCGCGGTGGCTCA | 388795 |
rs150713149 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881595 | CCCTCAGCTAGTATT[A/C]CTCCTTTTCTCCATT | 388795 |
rs150743879 | in-del | -/A | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860314 | AAAAGCAAAAAAAAA[-/A]CCCAGTTATTTTGTA | 388795 |
rs150763516 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940444 | AACTCCAAATGGATC[A/G]TAGACCTAAATGTAA | 388795 |
rs150854962 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874186 | TCAGCCTCCCAAAGT[A/T]CTGGGATTATAGGTG | 388795 |
rs150888980 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920403 | CGGTGTCTGGGGAGA[G/T]CTCCTGTATTAATTC | 388795 |
rs150906963 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931858 | CAAATAAATTACAGT[A/G]TAATATCTGGCACCA | 388795 |
rs150958328 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903933 | GGAGTGGTGGAGGAG[C/T]CGGGTCAGGGGTGAC | 388795 |
rs150991989 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958404 | TTGTGGTTCTGAGCA[A/G]TCTGGTCAAATCACA | 388795 |
rs150994399 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868707 | GTTGTTGGCTGGGAC[C/T]GGTGTGGTGGCTCAC | 388795 |
rs151010210 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900725 | GTGTGCGCCACCATG[A/C]CCGGTTAATTTTTTT | 388795 |
rs151029160 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883752 | CTGGAGTGCAGTGGC[A/G]CAATCTTGGCTCAGT | 388795 |
rs151030153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861821 | TCCATAATCTCACCT[A/G]CCAGAGATGACTGCT | 388795 |
rs151046269 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960275 | GAGGGTGGACAGGAG[C/T]CTTTGTCCTTTAACA | 388795 |
rs151052613 | in-del | -/AT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880898 | AACTGTGGGCAAAAC[-/AT]ATATATATATATAAA | 388795 |
rs151080904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942760 | TTTTGTAGGTGTTTT[A/G]TGATTTCATTGAAAA | 388795 |
rs151169872 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875585 | TCTCAGCTCACTGCA[A/G]CCTCTGCCTCCTGAG | 388795 |
rs151206915 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897363 | GCTTGGTGGGCTCCC[A/T]ATACATTTGCTGCAC | 388795 |
rs151223622 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933645 | CACCCCACCCTCTAA[A/G]CCTCTGGTAACCATC | 388795 |
rs151238819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914463 | TTGGCTATGTCTTTA[A/G]TGATTGTATTAGTTT | 388795 |
rs151256301 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923589 | CTCCAGAGGTAATTA[C/T]GTTAAGACATGTGTT | 388795 |
rs151261025 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864627 | CAAATGCAACACACC[C/T]GAGCCCCCTGATGTA | 388795 |
rs151283464 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871495 | ATGCTGTATTCCTTG[-/C]TTTTTTAAAAAATTA | 388795 |
rs151295353 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886061 | CCAGGCAGGAAATCA[C/T]AGTGGTTATGAGCAT | 388795 |
rs180773255 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943016 | TACTTGAATATGGTC[A/G]AATAAGTCCTCCTTT | 388795 |
rs180776769 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887768 | TCTGTGCACATGCTA[C/T]ACGAGTGCAGGATGC | 388795 |
rs180787035 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915077 | TAATTAAAAAAAAAA[A/T]TTTTTTATAGAGATG | 388795 |
rs180791700 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895828 | TGCCCGTCTCGCCCT[C/T]CCAAAGTGCTGGGAT | 388795 |
rs180792469 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935243 | TTTGCTCTTGTTGCC[C/T]GGGCTGGAGTGCATT | 388795 |
rs180806618 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953488 | AACCTTGCCAGCACT[C/T]GTTATTTTGTTTTTG | 388795 |
rs180808053 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927179 | AAATTTCAAAACTTA[C/T]AAATCTGACAATTAC | 388795 |
rs180810932 | snp | A/G | 0.000191902 | 0.00979357 | missense | EFCAB8 | GRCh38.p7 | 20:32867741 | GAGGACATCAACTCG[A/G]CTGGAGGTAAGGCCG | 388795 |
rs180844405 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907412 | TAGTGACCCCTCCTC[A/G]GCTGCCTGGCCATGA | 388795 |
rs180845360 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859099 | GGCTGGAGAGCAGCT[C/T]TTATCTGTGTCCTGG | 388795 |
rs180861182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876412 | CTCAGGAATAGGCCA[A/G]CCTGTGGCTGTTACA | 388795 |
rs180898922 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862592 | GCATTCTTGGGTACC[A/G]TTCAGTCTTCTCCCT | 388795 |
rs180905180 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919845 | TCCAGGACAAAGGAA[A/G]CATCTTCCCCAGAGG | 388795 |
rs180907314 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872964 | GAGTGTGATGGTGGG[C/T]GCCTGTAATCCCAGC | 388795 |
rs180911793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899948 | GGTATGTTCTCTCGC[A/G]GAGTCTTCCTGCTGG | 388795 |
rs180954262 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882121 | GAGAATTGCTTGAAC[C/G]CAGGAGGCAGAGGTT | 388795 |
rs181034600 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932755 | AGTGAATAGTGAATG[A/T]TATTTCACATATGTG | 388795 |
rs181048524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960758 | CGAAGGCCATGCCCC[C/T]GCAGGGCCCCCCTGT | 388795 |
rs181050419 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893109 | GCCTCCCAGAGTGCT[A/G]GTCTTACAGGTGTGA | 388795 |
rs181050551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938865 | AATTGATTTAATGCA[A/G]TTTATATCAAAATCC | 388795 |
rs181058253 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912483 | CTTAGCCAAGATGCC[A/G]GGGGTTGAGTACTGC | 388795 |
rs181086163 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948704 | TTTACCCCAGATATA[C/T]AAGGTTGGTTTAATA | 388795 |
rs181086916 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866102 | GTGCTCCTCTGTTGG[G/T]CTCCGTGGAGGCAGG | 388795 |
rs181096086 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935592 | GCTCACCACAACCTC[C/T]GCCTCCCAGGTTCAA | 388795 |
rs181098701 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954649 | AACTAGAGATTTTGG[C/T]TTTTAATTTAGCTCT | 388795 |
rs181138515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877260 | GTCGCCCAGGCTGGA[A/G]TGCAATGGCACGATC | 388795 |
rs181147288 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904870 | GACCTCAGGTGATCC[A/G]GCCGCCTTGGTCTCC | 388795 |
rs181153240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886531 | TCAGGGCTCATCCTT[C/T]GGGGAAGAAGAGGCC | 388795 |
rs181167701 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896289 | GGGGTGGGGGCACTC[C/T]GCTCAGCTCACCAGG | 388795 |
rs181181188 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859942 | GAATCGTGCATTGCC[C/T]TTAGTTGTTGGGTCT | 388795 |
rs181181941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941455 | CATTATTTATAATAC[A/G]AAAGTGGAAACAACC | 388795 |
rs181183525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924808 | GATTTGAGGCACTGT[A/G]GCTGGCAGGGCTGTG | 388795 |
rs181464431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930199 | AAAGACGCAAAATCC[C/T]TGCCCTCTAGTAGTT | 388795 |
rs181471649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910384 | GCACCTTGGTCCTGC[A/G]TGGAGTCTCTGGGTT | 388795 |
rs181545096 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890801 | ACCTCCCAGTGCCTC[A/G]CTTTACCCAGAGGTA | 388795 |
rs181550292 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871554 | ACTGAATGTATCTTG[C/T]AGATATTTTCATATC | 388795 |
rs181557531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867168 | CAAATGATCCGCCCT[C/T]CTCGGCCTCCCGAAG | 388795 |
rs181569267 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906108 | ACCACACGTAGCCAG[A/G]GTGGGGCACCCGGGA | 388795 |
rs181574449 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887440 | AATTAGCCAGGCGTA[A/G]TGGCGCACCCCTGTA | 388795 |
rs181627285 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920563 | CAGCAGCAAGAGAAA[A/G]TGAGAAGCAGCAAAA | 388795 |
rs181654924 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882467 | GTATCTCTTGCTTGC[A/G]TTCCCCAGGTAGCAA | 388795 |
rs181666852 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942533 | CTCTAAAAAAAAAAA[A/C]CAATAAAAATATATT | 388795 |
rs181667994 | snp | A/C | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32961464 | CAGCCCATTCCACCC[A/C]CTCGGTCCCATCCCC | 388795 |
rs181678537 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926032 | TCTCACTGTGAGCAC[C/T]GGATGCTGGCTACGC | 388795 |
rs181727360 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939747 | GTACCCAGGCTGGAG[C/T]GCAGTGGCGCCACCT | 388795 |
rs181737816 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901148 | GCTTTGAATGGGGCC[A/G]TGTGGCAGAAGTTTG | 388795 |
rs181775938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939418 | CTCCCAAGTAGCTGG[A/G]ACTACAGGCATGTGC | 388795 |
rs181785663 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947599 | CACATTTCTAAATAA[A/C]CCATGGGCCAAAAAA | 388795 |
rs181818885 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862913 | GCTGGGATTACAGGT[A/G]TGAGCCACTGCACCT | 388795 |
rs181931079 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875410 | GGCTGGAGCCATCTC[C/G]CTTCTGTGCCCCCTG | 388795 |
rs181967330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872357 | ATGAAGTGCCATCAC[C/T]GGCACATCTCAGTGC | 388795 |
rs181994580 | snp | C/T | 0.00438332 | 0.0466095 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32911584 | GCACGTGGAGATGAC[C/T]GCCATGGCCCTGGAT | 388795 |
rs182145142 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897526 | TGGCTCACTGCAGCC[G/T]TGACCTCCCGGGCTT | 388795 |
rs182152298 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879583 | CTGTAGGAAATGAAG[C/T]CCCTAAGAAACAGAT | 388795 |
rs182205972 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | EFCAB8 | GRCh38.p7 | 20:32961719 | TGTGGCTCTTCCCCC[A/G]GCCACCCCACTGGGC | 388795 |
rs182242626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892544 | GACAGCCACCAAATC[C/T]CAGCAGAGGCTTGTC | 388795 |
rs182272253 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931420 | ACTAACTCATACCCA[A/G]GAGAAATACACTTAC | 388795 |
rs182344440 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913473 | AATATATGAATTTTG[A/G]GAGCAAAATTCAGTC | 388795 |
rs182353220 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940031 | CCTCCCTCCCTTCCT[C/T]CCTTCCTTCCTTCCT | 388795 |
rs182354578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922524 | GGGGCAAGATAGACA[A/G]TTAACCAGCAAATAA | 388795 |
rs182389419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958245 | CTGGCTCATCCACAC[A/G]TTTGTTGAGTACTCA | 388795 |
rs182390664 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937257 | AGTGCTGGTATTAGA[A/C]GCATGAGCCACTGCC | 388795 |
rs182394794 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917178 | GCTTCAGCCCAGCTC[C/T]GACACCTGAGAGTAT | 388795 |
rs182563025 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888331 | CCCGGGTTCAGGTGA[A/T]TCTTCTGCCTCAGCC | 388795 |
rs182569953 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869046 | TGACTGGGGAAGAAC[A/C]CACTTCCAAGCTCAC | 388795 |
rs182684957 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933934 | GTGAGCCGAGGTTGC[A/G]CCACTGCACTTCAGC | 388795 |
rs182730868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949540 | CAGTGTGGTAATGGC[A/G]TAGAGACAGACAGAC | 388795 |
rs182753731 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863747 | CGTGGTCCTTACAAC[G/T]ACTGGAGTTAAGTTG | 388795 |
rs182769173 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902493 | GGCTCACTTCTGTAA[C/T]CCTAGCACTTAGGGA | 388795 |
rs182777825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943493 | CGCAAGCAAGTTCAT[A/G]TGGAATGCATCTAGA | 388795 |
rs182783981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879822 | ACATACTGCTTCTCA[A/G]ATTCCTTTAGTTTAA | 388795 |
rs182791769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907765 | GCTGAGGTCCCCAGT[C/T]GGCCATGGGCAGAGG | 388795 |
rs182957893 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865088 | CTGGGGCTCTGCAGC[C/T]GTGTGCTTCCCCTCA | 388795 |
rs182958716 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951112 | TGGGAATATAAAATG[C/G]TTCAACCACTTTGGA | 388795 |
rs182972278 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933254 | TTAGTTTTATAATGA[G/T]ATATTTTAAACAATT | 388795 |
rs182975320 | snp | A/G | 0.000990857 | 0.0222362 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912783 | GTTCTGTTTTCTTTC[A/G]TCTTCAACAGATTAG | 388795 |
rs182986277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893730 | TGGGCAGGGGCTGTC[C/T]TGGATGTGGGCTCTG | 388795 |
rs183009562 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884785 | GGCTCAAAGATTGGG[C/G]AGATCAAGTAGGAGA | 388795 |
rs183053927 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898824 | CAAAACTCAGCATAG[A/C]AGCCAGCACAGAGTG | 388795 |
rs183062600 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923608 | AAGACATGTGTTGTA[C/G]CCTTCTAGAATTTTT | 388795 |
rs183074040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927492 | TGGGATTAAAGGTGC[C/G]CGCCACCATGCCCAG | 388795 |
rs183084373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921671 | TCAACAGCAGCATTC[A/G]CTGCTAACAGGTTGG | 388795 |
rs183099016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861192 | TTGGTTTTTGCTCCT[A/G]TGAATGATGCTGCAG | 388795 |
rs183105545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863534 | AACCCCATGGCTTCT[A/G]CAGGACAACTCCTCT | 388795 |
rs183136869 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901860 | GCCCGGCTAATATTT[C/G]CATTTTTAGTAGAGA | 388795 |
rs183143184 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945300 | AGCTGGGACTACAGG[G/T]GCATGCCATCATGCC | 388795 |
rs183143804 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883714 | TTTTTTTTTGGAGAC[A/G]GAGTCTCACTCTGTC | 388795 |
rs183171243 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869643 | AAGTCACAGGTCCCA[A/C]CACACTCCAGGGGAG | 388795 |
rs183187908 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928245 | CTGATTTTTTATTTT[A/T]TTTTTTTTGAGACAG | 388795 |
rs183198862 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908750 | TTCCTTGTCTCAGTC[A/G]TGAGCCTCATAACTC | 388795 |
rs183319013 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940045 | TTCCTTCCTTCCTTC[C/T]TTCCTTCCTTCCTTC | 388795 |
rs183337034 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936986 | CTTAAACAATGTTTT[A/T]GTTTCCAGTGTACAG | 388795 |
rs183339249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903208 | GTGCCCACCACACCG[A/G]CCTTGCATAGGCTGC | 388795 |
rs183340379 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916523 | CTTGGCCCCTCAAAG[G/T]GCTGGGATTATAGGC | 388795 |
rs183356538 | snp | C/G | 0.000191663 | 0.00978747 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885684 | ACATGGGTGATTGGA[C/G]AGCCTCTGCCTTAGC | 388795 |
rs183453146 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860339 | CCAGTTATTTTGTAG[A/C]ATATCCTGTAATGTG | 388795 |
rs183600204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896885 | ACAGTTGAGTCACCC[C/T]GGTAGCTTCTCATCA | 388795 |
rs183639279 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936324 | CACGTGTGAGCCACC[A/G]CGCCTGGCCTATTTT | 388795 |
rs183642111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913247 | AGTTCCAGACAAGGT[A/G]CCAGCAGATTTGGTG | 388795 |
rs183660018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873882 | CTATTTGTTGCCATT[A/G]TATACTTTTGTTCTG | 388795 |
rs183678762 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950474 | TTTATTTTAAATAAA[C/T]CTGAGAGGGGCGGCT | 388795 |
rs183790425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895165 | GTGCTGGCTCTACTC[A/G]TCTGTGTCAGACTGG | 388795 |
rs183797742 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875064 | TGGTTCTCCTTTTCT[C/T]TGGAGAGTTTTCTTT | 388795 |
rs183816583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915924 | GTGATCCACCTGTCT[C/T]AGTTCCCAAAGTGCT | 388795 |
rs183821878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909707 | TGGAATCAGGCCTGC[A/G]TGTGGTCAGGACGTC | 388795 |
rs183829086 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878242 | TTGCACTCCAGCCTG[A/G]GTGACAGAGCAAGGC | 388795 |
rs183832575 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890503 | GACTGGAAGGTCAGG[G/T]ACTGCATCTGTTCTG | 388795 |
rs183839899 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955716 | ATATATCTTCTGTTC[C/T]ACGTCCTGAGCGAGG | 388795 |
rs183842321 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871339 | AGTGCAGTGGTGTGA[A/T]GATAGTTCACTGAAG | 388795 |
rs183868487 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894075 | CTAGATCCCCAGAGG[A/T]TACGGCTCAGGGCCG | 388795 |
rs183904356 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933671 | CCATCATTCTCCTTT[C/T]TACTTCTTTTTAAAA | 388795 |
rs183920995 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940974 | AATGTAGAAAGCTGG[C/T]CAGGTACGGTGGCTC | 388795 |
rs183946398 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957629 | CCTCCCTGGTGCTCG[C/G]CAAATGTCCTAACAA | 388795 |
rs184035694 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895579 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTAAGGC | 388795 |
rs184061652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951882 | TGCTTTATTCTGGAT[A/G]CAAGTTCTTGATCAG | 388795 |
rs184063691 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934212 | TGCAGTATTTTTCTT[C/T]CATGACTGGCTTATT | 388795 |
rs184070291 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886607 | ACCAAGGGGGAGTCA[C/T]GATCACCATCCTGAG | 388795 |
rs184079603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914045 | ACTTCCCTGCATGAG[C/T]CCCCTGGCCCTGTGG | 388795 |
rs184152098 | snp | A/G | 9.04773e-05 | 0.00672536 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32961249 | GCACATCCGCCTGGT[A/G]GCCCACCATGTCCAG | 388795 |
rs184175865 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939115 | CCTTCCTTTCTTTCT[C/T]TCTTTCTTTCTCTTT | 388795 |
rs184394114 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870927 | GCAGTGGTGCGATCT[C/T]GGCTCACTGCAACCT | 388795 |
rs184432139 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890971 | AGAAAGTGGTCAGCC[A/G]TCAGCAAGGGCTAGA | 388795 |
rs184447059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946955 | TCTTTGTTGTTGAAC[A/G]TATCAGTAGTTTGTT | 388795 |
rs184461999 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904354 | CCCCCAGGCTGGAGT[A/G]CAGTGGCATGATCAC | 388795 |
rs184462647 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930221 | CTAGTAGTTCATAGT[C/T]GAGTATGACGTTCCT | 388795 |
rs184465471 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910526 | GCTCTGGACAGGTGC[A/G]CCGCATCGGCTGCAG | 388795 |
rs184523555 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866026 | AGGAAGAAGAGGGAA[G/T]AGCTGAAGGCGGTGC | 388795 |
rs184582583 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924485 | ATGTGAAAAGAATGT[C/T]TAATACATCTGAAAA | 388795 |
rs184600553 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886386 | CTTGGTCGCCAGGGC[C/G/T]GTCCAGAATCCTCCA | 388795 |
rs184689341 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861578 | ACAGATGTGAGCCAC[C/T]GCGCCTAGCCGTTGA | 388795 |
rs184705411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945830 | AGACTTACGCATGTA[A/G]ATTCGCAATTACAGG | 388795 |
rs184752737 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923889 | ATTGCAATGAATACC[A/C]TTGTACATAAATTTT | 388795 |
rs184754848 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903813 | GGGCTAGCAGTGGCC[A/G]TGGGAGTGGAGGGAA | 388795 |
rs184760636 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865520 | TGCTGCCTAGAAGCC[A/G]GGCGCAGTGGCCCAT | 388795 |
rs184764013 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885941 | TTTCCTTCTCTTGCG[C/T]CCCCATCTCAGTGAA | 388795 |
rs184793149 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925170 | AGGAAGGAGTCCAGG[A/G/T]TGCAGATCCAGGCCC | 388795 |
rs184857092 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929593 | GTGATTCACCCGCCT[C/T]GGCCTCCCAAAGTGC | 388795 |
rs184888081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940566 | TACAAAAGAAAAAAA[C/T]AGATAAATTGGACTT | 388795 |
rs184902637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941731 | AATTGCGTAGTGACT[A/G]CTGGGTAAAGAGTTT | 388795 |
rs184933627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938626 | AAAACCAATATATTT[A/G]TATACACTAGCAATA | 388795 |
rs184935812 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960567 | CCAGGCCCATAGTAA[A/G]AGACAGGGTAAACGG | 388795 |
rs184946810 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875263 | CATGTGAGGACAGAA[A/G]CGTCCGGAATTGGCC | 388795 |
rs184963659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905272 | AAGGCAGATGAACAA[A/G]AGAAAAGCATGCACA | 388795 |
rs184999885 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919558 | CTAGAGTGCAGTGGC[A/G]TGGTCTTCGCTCAGT | 388795 |
rs185002950 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899162 | AAGCCGAGGTGGGTG[A/G]ATCATGAGGTCAGGA | 388795 |
rs185188816 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953913 | CCTCCTGGGTTCAAG[C/T]GATCCTCCTGCCTCA | 388795 |
rs185269369 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937979 | ATGAGGCCAGTATTA[C/T]CTTGATACCAAAACC | 388795 |
rs185285508 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871940 | GCAGTTTGACTCCCA[A/G]CTCTGTCTGGAAGGA | 388795 |
rs185292508 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899100 | TTTTGAAAAACTAGT[C/T]AGTCACCGGGCGCGG | 388795 |
rs185398602 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875760 | GTGATCCACCTGCCT[A/C]AGCCTCCCAAAGTGC | 388795 |
rs185401683 | snp | A/G | 0.00100979 | 0.0224472 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918577 | TGTGCCCCAGCAGGT[A/G]GGAGCGAGAGCCCAA | 388795 |
rs185416260 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876662 | AATCCTATGGGGTAG[G/T]TGCTATTACTTACCT | 388795 |
rs185428238 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959399 | TGACTCCTATGCTTC[C/T]ATCAAGGCATACATC | 388795 |
rs185439582 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935446 | CTCAAGTGATCTGCC[C/T]GCCTTGGCCTCCCAA | 388795 |
rs185443612 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915083 | AAAAAAAAATTTTTT[A/T]ATAGAGATGGGGTCT | 388795 |
rs185447925 | snp | C/T | 0.00795532 | 0.062565 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859130 | CTGGCTTTCAATGCA[C/T]GTATCCTTAAGTCAT | 388795 |
rs185458184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896097 | CAGAACAAAAAGAGC[C/T]TAGAGTCTCAATTCC | 388795 |
rs185467914 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880435 | CACCATGCCTGACTA[A/T]TTTTTTTGTATTTTT | 388795 |
rs185518344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914722 | AGAACAGCATGAGGG[A/G]AACTGCCCCCATGAT | 388795 |
rs185523752 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866811 | CCTCCCTCCCTCCCT[C/T]TCTTCCTTCCTTCCT | 388795 |
rs185548172 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952722 | AGTGTATCACTTGCC[C/T]GTTCATTTTCCTGAT | 388795 |
rs185620593 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889556 | CTTAGTGCCAAGTAG[G/T]CAGGGGGTGGTCGGT | 388795 |
rs185649045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934740 | AGGGCAGTTCCCCTG[C/T]TCATGCTCTCTTGCC | 388795 |
rs185649494 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928741 | GCAGAACTTCCAGTA[C/T]TCTGTTGAATAAAAG | 388795 |
rs185659401 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895805 | TGAACTCCTGACCCC[A/G]GGTCATCTGCCCGTC | 388795 |
rs185662066 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873424 | AAAAAAAAAGTTGTA[A/G]ACAGGGGTTATTGAC | 388795 |
rs185681258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932865 | TTCTTGCAGTCTTAT[A/G]TGCCTTTTGAATCTC | 388795 |
rs185695352 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912550 | CCAGGTCACTTGCCC[A/G]TTTCCCAGCTATCCT | 388795 |
rs185701141 | snp | C/T | 0.00383568 | 0.0436248 | missense | EFCAB8 | GRCh38.p7 | 20:32893184 | TGCAGGTCTGACTAT[C/T]ACAGAGGTGTGTTCT | 388795 |
rs185711528 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915845 | CCTGGCTAATTTTTT[A/G]TATTTTTAGTAGAGA | 388795 |
rs185744238 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909174 | TGTGTGTCATCCTTA[C/T]GCACTTGGCTGGCCC | 388795 |
rs185745789 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955156 | AGGCCCCTCCCTCCC[C/G]CTAAAGCCAAACCCA | 388795 |
rs185747485 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935643 | TCCCAAGTAGGTGGG[A/G]TTACAGGCATGCGCC | 388795 |
rs185778612 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945557 | TTTTATTACGGTTAC[C/T]TAGAATTCTTTGTCA | 388795 |
rs185806106 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943348 | GGTAAACAATGTAGT[C/G]ATATGCAAGTCATAT | 388795 |
rs185825194 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907441 | GAGGGCTGGGCTTGG[A/C]CTTTCCCACATGCCA | 388795 |
rs185942395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927340 | TTGTTTATTTATTTA[C/T]TTATTTAATTTAAAA | 388795 |
rs185992189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933277 | AAACAATTGGGATTA[C/T]ATTGTATGTAACTGG | 388795 |
rs186004098 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882686 | CCACCACGCCTGGCC[A/G]ATTTTTTGTTGTTGT | 388795 |
rs186011913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863299 | TATATTCCCAGAGCA[A/G]AGCTCTGTTCTGTCT | 388795 |
rs186213516 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888318 | GCAGCCTCTGCCTCC[C/G]GGGTTCAGGTGATTC | 388795 |
rs186217037 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887484 | GGGAGGCTGAGGCAC[A/G]AGAATCACTGGAACC | 388795 |
rs186238773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867219 | GCCACCATGCCCAGC[C/T]CCCTGGGGTTCTGAA | 388795 |
rs186242734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942717 | TGTTTATCACTTTCT[C/T]AGAGAAAAGATAAAT | 388795 |
rs186252726 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860403 | CATGTATTTTTTTGG[C/T]AATAATACTACTGAA | 388795 |
rs186268705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884254 | TTACTGAGCCTGGGC[C/T]GGGTGCACCAAATGC | 388795 |
rs186275349 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949062 | ATTTGTAGTTGACTA[A/C]TTGTCTATGTAGAAA | 388795 |
rs186284168 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863682 | CCACCCTCTCCCTTG[A/G]CCTTGACTTCTTTTC | 388795 |
rs186290909 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940007 | CCTGCCTGCCTGCCT[C/G]CCTCCCTCCCTCCCT | 388795 |
rs186307520 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920072 | GGTGCCCATCTTTCT[G/T]TCCAGAAACCTTCCA | 388795 |
rs186308670 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921951 | TCTCCTGCCTCAGCC[A/T]CCAGAGTAGCTGGGA | 388795 |
rs186321403 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862723 | ACCTCTGCCTCCCAG[C/G]TTCAAGCAATCCTCC | 388795 |
rs186323280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882154 | AGTGAGCCGAGATTG[C/T]GCCATTGCTGTCCAG | 388795 |
rs186361042 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896736 | CCTCTCACTACCGCC[A/G]TTGCTAAGCCCTGGT | 388795 |
rs186408541 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860033 | ATTTTGGCCAGGCGC[A/G]GTGACTCACGCCTGT | 388795 |
rs186498151 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900790 | GTCCAGGATGGTCTC[A/G]ATCTCCCAACCTTGT | 388795 |
rs186523866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898112 | GAGGGTGGCAGTGGG[C/T]TGGGAGCACAGCCCA | 388795 |
rs186544715 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879614 | AACCTGAGGGTTTTC[A/G]TGCTAGGTTCAATGG | 388795 |
rs186554270 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860484 | TTGTTCCATCGCTGA[C/T]GGTGGTAACTTTTTT | 388795 |
rs186560438 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957735 | TCTCTCTCTCTAAGC[C/G]AAGTCTGATTCTCAT | 388795 |
rs186565746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937009 | GTGTACAGATCTTTT[A/G]ACTTCTTGGTTAAAT | 388795 |
rs186570042 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916534 | AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACCA | 388795 |
rs186579088 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877398 | ATTTTTAGTAGAAAC[A/G]GGGTTTCACCATGTT | 388795 |
rs186828263 | snp | A/G | 0.00119737 | 0.0244387 | missense | EFCAB8 | GRCh38.p7 | 20:32961580 | ACCTTCATGTCCTCT[A/G]TGAAGGGGAGCTCCC | 388795 |
rs186842351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921045 | AATACAAATCATAGT[C/T]GAGTTAGGGTGTGGC | 388795 |
rs186909876 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901348 | AATCACAAAAAAGTC[G/T]CATAATGTTATAAGA | 388795 |
rs186922172 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895364 | AGGTCATACTCTGTT[A/G]CCCAGGCTGGAGTGT | 388795 |
rs186928740 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875120 | TGTATGGAAATGGGA[A/G]TTGGTCTTTTTTAGT | 388795 |
rs186929605 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933853 | CATGGTGATGCGTGC[C/T]TGTAATCCCAGCTAC | 388795 |
rs186948493 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951245 | AAATGTTCACAGCAG[C/T]ATTTTTTTGTGACAG | 388795 |
rs186954219 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933990 | TCAAAAAATCAATCA[A/G]TCAAATCAAAGCAAA | 388795 |
rs186958347 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913855 | CCTTAAATCTCAAAG[A/G]TAATCCTCTTTGGCT | 388795 |
rs187098213 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955719 | TATCTTCTGTTCCAC[G/T]TCCTGAGCGAGGGTA | 388795 |
rs187165701 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916294 | ACAGGATCTTGCTCT[A/G]TTGCCTAGGCTGGAG | 388795 |
rs187176613 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878556 | CGCTCTGTCGCCCAG[A/G]TCGGACTGCGGACTG | 388795 |
rs187182871 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869323 | GCTCACTGCAACCTC[C/T]GCCTCTGGTTCAAGC | 388795 |
rs187188040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931888 | AGAAGTGAATTTACT[C/T]ACTACAAAATGGAGA | 388795 |
rs187188534 | snp | C/T | 0.000798403 | 0.0199641 | missense | EFCAB8 | GRCh38.p7 | 20:32958474 | GCCTGTGATGGTCCT[C/T]GTGAAAACAGAGCAA | 388795 |
rs187202777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927868 | ACATAAAATTTACCA[C/T]TGAAACCATTTTTAA | 388795 |
rs187209522 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908172 | AGTGCTTGGACGGAC[A/G]ATGTGCCCTGGCCTT | 388795 |
rs187222022 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888836 | GGTGGCTTCTGGCCT[G/T]TTGCTCTAATAGCAG | 388795 |
rs187281237 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936364 | TACCTGTGCTTTTGG[A/G]GTCATAGCTAAATAA | 388795 |
rs187375223 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896943 | CCATGGCCGTCAGGA[C/T]GTGAGGTGATCTGGC | 388795 |
rs187389870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948145 | ATATCAGGAATGAGT[A/G]AGATGACATCATTTC | 388795 |
rs187394360 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885860 | CCATTCCCTGTGGGT[A/G]TCTCACAGGCCCCTC | 388795 |
rs187409690 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912253 | ACCAGCCTGGCTAAT[A/G]TGGTGAAACTCCCGT | 388795 |
rs187421841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865336 | ACGTGAGTAAGCACC[A/G]AATGCTTGCTGGGCT | 388795 |
rs187423725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903354 | CTTCTGTTGTCCTCC[A/G]TCAAAGCCATGTGCT | 388795 |
rs187445389 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945586 | CAAATAATTAATATA[C/T]CTCAATTTCTTTAGC | 388795 |
rs187502158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909436 | AAAGTGCTATGTGTT[A/G]TGGTAGAGTTGTGCT | 388795 |
rs187517464 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870928 | CAGTGGTGCGATCTC[A/G]GCTCACTGCAACCTC | 388795 |
rs187563558 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872403 | GGGGACCAATGTTTG[A/T]TGAAGCCAGGACCCA | 388795 |
rs187694695 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929067 | CCTTTTAATATGCTA[C/G]TGAATGCAGTTTGCT | 388795 |
rs187760246 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889580 | GGTCGGTGAATGCTC[A/G]AATGAATACAGTGAT | 388795 |
rs187801881 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928274 | AGAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTA | 388795 |
rs187815487 | snp | A/G | 0.000668162 | 0.0182657 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889265 | CTGGCCTGAGTATGC[A/G]TCCCAGCCCATCTCC | 388795 |
rs187833890 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945474 | GTTTGGTTCTTTTCT[A/G]TATTTTCTGTGTCTT | 388795 |
rs187899408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922680 | TTCACAGAGGAGGTG[A/G]CATCTGCATAGAGCC | 388795 |
rs187962878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885493 | TCTTCTCTCTTTCAT[C/T]GCCTCCCACAGGAAC | 388795 |
rs187987175 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861478 | ATTTTTAGTGGAGAT[C/G]GGATTTCTCCATGCT | 388795 |
rs188008045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898841 | GCCAGCACAGAGTGA[C/T]TGGCAGTCAGTGAAA | 388795 |
rs188043683 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923946 | AAACTCTAGGATTAG[A/C]AACATACTCCTGGAA | 388795 |
rs188054780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904173 | AATTTTTAATTTTTT[C/T]GTACAGATGGGATCT | 388795 |
rs188087202 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940682 | TATCTGATAAGGGAC[C/T]AGTATCCAGAATATA | 388795 |
rs188099444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919669 | GCCTGGCTAAATTTT[C/T]TGTATTTTTATTGGA | 388795 |
rs188107489 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899297 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 388795 |
rs188113066 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882041 | TGTCTCTACTAAAAA[C/T]ACAAAAATTAGCTGG | 388795 |
rs188135470 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960624 | GAGCAGGGGATGTTC[A/G]AAAGAGCAGATTTGA | 388795 |
rs188135554 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938753 | TGAAAATTGCATAAC[A/G]TTATGGGAAGAGATG | 388795 |
rs188138483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937401 | TGTTGGACATTAATG[C/T]GGTTTCTAACTTTTC | 388795 |
rs188157306 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862587 | TTAGAGCATTCTTGG[A/G]TACCGTTCAGTCTTC | 388795 |
rs188165788 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940035 | CCTCCCTTCCTTCCT[C/T]CCTTCCTTCCTTCCT | 388795 |
rs188188219 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902692 | ACCACTTGCTGGTCT[C/G]CCGTTTTGGCGATGC | 388795 |
rs188223010 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864302 | TAAAGGGCTGCCTGA[G/T]ACTGGGTATGGTGGC | 388795 |
rs188257746 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940270 | TAAAAAATAAATTCT[C/T]ACATTATGATCAATT | 388795 |
rs188296906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880087 | GGAGCTGGGTCCTGA[A/G]ATACAAGGTGTGGCA | 388795 |
rs188339536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935491 | AGGCATGAGCCACTG[C/T]ACCTGGCCACTTTGC | 388795 |
rs188341380 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915141 | CTCTTGGTTTCAAGC[A/C]ATCCTCCTGTCTTGG | 388795 |
rs188351684 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896119 | CTCAATTCCTTCTCC[A/G]CTCCAGCAAAGATGG | 388795 |
rs188380877 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954517 | CCTGTACCACACTGT[C/T]TTGATTCCTGTAGCT | 388795 |
rs188428763 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917208 | TCCTCCTCTGAGTCG[C/G]CTCCCAGAATCCTCA | 388795 |
rs188435098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944171 | ACCCATATAGCCACC[A/G]TTCATGTCAAGAAAT | 388795 |
rs188437954 | snp | A/C | 0.00240027 | 0.0345597 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32960140 | GTCCACCAGGGTGCC[A/C]TATGGCTGGATGAAG | 388795 |
rs188502175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873651 | GCGGATCACTTGAGG[C/T]CAGGAGTTTGAGAGC | 388795 |
rs188527946 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893840 | TGCATCACCTCCCAT[A/T]ATCCGCCCCTACTGT | 388795 |
rs188544850 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923628 | CTAGAATTTTTTTGT[A/G]CATATACAAGTACAT | 388795 |
rs188604695 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876736 | CTTTGGGAGGCCAAG[C/G]GGGGTGGATCGCTTG | 388795 |
rs188694292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910100 | GACACAGAAAGCAGC[C/T]CTACAGATGGGCTGG | 388795 |
rs188704413 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890536 | CAACTCAGTGTCTCA[G/T]TGCCTGGTACCTTCT | 388795 |
rs188713406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871466 | TTTATTTTCTGTAGA[A/G]ATGGTGTCTTGCTAT | 388795 |
rs188728572 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946695 | TTTAAAAGTATATAG[G/T]TCTGTGAGGTTTCAT | 388795 |
rs188732845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930190 | GTGAACAAAAAAGAC[A/G]CAAAATCCCTGCCCT | 388795 |
rs188746641 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952019 | AATACCAGCACTTTG[G/T]GGGGCCAAAGTGGGT | 388795 |
rs188746925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905721 | GCCAAGATCGCACCA[C/T]TGCACTCCAGCCTGG | 388795 |
rs188750763 | snp | A/G/T | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934656 | GGAGGTAATTGAATC[A/G/T]TGGGGGTGGGTTTTT | 388795 |
rs188755558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887110 | CCTCTGTGCTCTTGG[C/T]GCTCTCTGAGTTCTG | 388795 |
rs188771713 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867017 | CCACCTCCTGGGTTC[A/G]AGTGATTCTCCTGCC | 388795 |
rs188790701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925329 | GGTTCAAGTGATTCT[C/T]GTGCCTCAACCTCCT | 388795 |
rs188815052 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894746 | TTTGGTATAAGAAAC[G/T]TGGAACGTTAGGCAC | 388795 |
rs188949130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933703 | CCTCTTTTTGGCCGG[A/G]CTCAGTGGCTCAAGC | 388795 |
rs188988577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947303 | CTCTCAATTTATAAA[A/G]CAACTATACAGAAAA | 388795 |
rs189002436 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930759 | AGCGAGGAGTCCTCT[C/G]CTGCTCTGCTAAGCC | 388795 |
rs189035261 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869817 | ATATCCTAAGGAATT[C/T]TCCATATTGCTACAT | 388795 |
rs189080581 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913365 | GCCTCCTTTATAAGG[G/T]CACTAATCCCATTCA | 388795 |
rs189102158 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874111 | TTTTCTGTGAAGATG[C/T]GGTTTCACCATGTTG | 388795 |
rs189141160 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948584 | AAAGAAAGAAAGAAA[A/G]GAAAGGAAAAGAAAG | 388795 |
rs189214346 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950752 | ACTGGAGCCCATTGT[A/T]TGAGGGTGAAGTTTA | 388795 |
rs189241921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924741 | TATCATGAATCTTGA[C/T]TGAATTTTTGGCCAC | 388795 |
rs189295914 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932116 | GGGCACGGTGGCTCA[A/T]GCCTGTAATCCCAGC | 388795 |
rs189372555 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880454 | TTTTGTATTTTTAAT[A/G]GAGATGGGGTTTCAC | 388795 |
rs189404330 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862040 | ATTCTCCTAGCTGTC[C/T]TGTGTGTTTCTCCCT | 388795 |
rs189410720 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899112 | AGTTAGTCACCGGGC[A/G]CGGTGGCTCACGCCA | 388795 |
rs189514531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886471 | ACAGCCCCCAGATGA[A/G]GGGCTTTCTGAGCCT | 388795 |
rs189521809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941423 | CATAAAATCTTGTAC[A/G]TGAATGTTTATAGTA | 388795 |
rs189546818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902293 | GTTGAGGCTGCATAG[A/G]ATGGTGGCCTGGAGC | 388795 |
rs189617319 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875800 | AAGCATGAGCCACCG[C/T]GCCTGGCCGTAGATG | 388795 |
rs189625599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886155 | TGGACAAGGTACTAT[A/G]TACTCCCTGTGCCTC | 388795 |
rs189676799 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940023 | CCTCCCTCCCTCCCT[C/T]CCTTCCTTCCTTCCT | 388795 |
rs189680502 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921954 | CCTGCCTCAGCCTCC[A/T]GAGTAGCTGGGACCA | 388795 |
rs189705742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939321 | AGAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG | 388795 |
rs189777565 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904712 | GCTCACTGCAACCTC[C/T]ACCTCCCAGGTCCAG | 388795 |
rs189778703 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900859 | AGGCGTGAGCCACCA[A/T]GCCCGGCTTAATTTT | 388795 |
rs189789090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862803 | CGGCTAATTTTTTAT[A/G]TTTTTAGTAGAGACA | 388795 |
rs189795672 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866027 | GGAAGAAGAGGGAAG[A/T]GCTGAAGGCGGTGCT | 388795 |
rs189814543 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914095 | TGGCTCTGCTGGGAG[A/T]CCCTGTCCTTTGAAA | 388795 |
rs189823101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942091 | AGCCTGTTTTTTTTA[C/T]CTTTGACAACCTAAA | 388795 |
rs189875714 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875374 | GGCTGGAGGAGGCAG[A/C]CTCCTAAGGGCCCCG | 388795 |
rs189947728 | snp | C/T | 0.000798403 | 0.0199641 | missense | EFCAB8 | GRCh38.p7 | 20:32961308 | CTGTGCTGGATACCA[C/T]GGACAGCACGCCTGC | 388795 |
rs190022806 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920335 | ATTCTCCCCAGTGCC[C/T]GGAAGGCATCTTGGA | 388795 |
rs190037507 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882214 | CAAAAAGAAAAAAAA[A/C]AACAGCATGCAAATG | 388795 |
rs190119245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895654 | TTGGCTCACTGCCAC[C/T]TCTGCCTTTCGGGTT | 388795 |
rs190161958 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859175 | TCGTACAAACCACTC[A/G]TTCCCCTCTCATCCC | 388795 |
rs190306860 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911228 | GATTATTTTCTTTGG[C/G]TAGATCCTGATAAGT | 388795 |
rs190314132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891339 | CCGTGTTTGTTGGCT[C/T]ATCAGGTGTCTGGGA | 388795 |
rs190320518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919290 | TTGAGTGAGAAACAC[C/T]ACCGTCCCCAAACAC | 388795 |
rs190346431 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933177 | CAGTAGCAACCAGTG[C/T]AGACCTGAGACTAAA | 388795 |
rs190352794 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912613 | CTCACTCCCCTAAGT[C/G]CATCAAATGAGGGAA | 388795 |
rs190362973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893421 | TCTCTGGGAAGGCGT[C/T]TGCTTCCAAGCGCAG | 388795 |
rs190394030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949319 | AATGGGTAGAAGACT[C/T]TCTGATTAAGAATAA | 388795 |
rs190404797 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865766 | ATCGCACCACGCTCC[A/G]GCTGGGTGACAGAGT | 388795 |
rs190423940 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873434 | TTGTAGACAGGGGTT[A/G]TTGACCCATTTGCAG | 388795 |
rs190471563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869626 | TTCTGTTGGTTAGAA[A/G]CAAGTCACAGGTCCC | 388795 |
rs190551194 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901540 | AGGGCCAGGAGGGCC[A/T]CTGTGGGCCGGGCCT | 388795 |
rs190562005 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882718 | GTTGTTGTTTTGAGA[C/G]AGAGCCTTGCTCGGT | 388795 |
rs190562027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934873 | TAAATTACCCAGTCT[C/T]GGATATGTCTTTATT | 388795 |
rs190563190 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938067 | TACAAAAATCTTCAA[A/C]ATACTAGCAAATTGA | 388795 |
rs190574661 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863505 | CATTAAGTCAGGAGT[A/G]AAGAAACTTGTGAAA | 388795 |
rs190575829 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871972 | GCCGCAGGGCTCATG[G/T]CCTGCCCCCTGGCAT | 388795 |
rs190585711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895818 | CCAGGTCATCTGCCC[A/G]TCTCGCCCTCCCAAA | 388795 |
rs190587557 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928006 | CCTCTCCCTCCAAAC[C/G]CTGGAAACCCCCATT | 388795 |
rs190591592 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955455 | TGAGGCAGGAGGATC[A/G]CTAGAGCCCAGGTGT | 388795 |
rs190592794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921106 | CAGGACTTGAGAACA[A/G]GAGGGCAGTGCCCTG | 388795 |
rs190594199 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872559 | TTGGGATCCCAGCGA[G/T]CTGAGGTGGGTGGAT | 388795 |
rs190600728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908656 | TGTCCCCACTCAGGC[A/G]TCCTCAGCCTCTCCC | 388795 |
rs190608920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888975 | TGGGGGGCGGGGGGC[A/G]GACAGGGTCTCACTC | 388795 |
rs190619677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884261 | GCCTGGGCCGGGTGC[A/G]CCAAATGCAGCCTCT | 388795 |
rs190623520 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912302 | AAAAATTAGCCAGGC[A/G]TGGTGGTGGCTGCCT | 388795 |
rs190633988 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944222 | GCTCACTACTGTAAT[A/C]CCAACACTTTTTTGT | 388795 |
rs190654062 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950399 | CCAAATTTGAAGAGA[A/C]TTCACTGTAAGAATT | 388795 |
rs190751334 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953061 | TACTCACCTAAGTAG[A/G]ATAATACAATAGTCA | 388795 |
rs190827972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914945 | ACTCTGTCACCCAGG[C/T]TGGACTGTAGTCATG | 388795 |
rs190832529 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888330 | TCCCGGGTTCAGGTG[A/G]TTCTTCTGCCTCAGC | 388795 |
rs190838633 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892867 | TTTTTATGACTCAGA[A/G]TCTCACTCTGTGTCC | 388795 |
rs190842619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863745 | CACGTGGTCCTTACA[A/G]CGACTGGAGTTAAGT | 388795 |
rs190860679 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927356 | TTATTTAATTTAAAA[G/T]TTTTTTGAGACAGAG | 388795 |
rs190995032 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897434 | ATCCAACAGGCCTGC[A/G]CTGACTTTTTTTTTT | 388795 |
rs190999486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942951 | TCTGAGCTTTCTATT[A/G]TCTTCCATTGCTTTG | 388795 |
rs191003972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878587 | CAGTGGCGCAATCTC[A/G]GCTCACTGCAAGCTC | 388795 |
rs191009804 | snp | C/T | 0.00142089 | 0.0266162 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32906872 | GATGCCTTCATCCGC[C/T]TGTGGAACCCCTTTG | 388795 |
rs191059139 | snp | C/T | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860439 | GTGCCCTGCATGTAT[C/T]GGATCAGGAGGTGTG | 388795 |
rs191091035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868920 | AATCTGGGAAGCAGA[A/G]GTTGCAGTGAGCCAA | 388795 |
rs191107653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943461 | GGGCCAGAGAAGTGC[C/T]GGGACCTATGTAAGG | 388795 |
rs191126333 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907745 | ATGGGGACAGGGACA[G/T]TCTCGCTGAGGTCCC | 388795 |
rs191241492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895003 | GTGACTTTGCAGCAG[C/T]ACAATGTTTGGCATG | 388795 |
rs191251694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874625 | CGGTTCACTGCAACC[C/T]CTGCCTCCTGGGTTC | 388795 |
rs191287750 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937223 | GACCTCAGGTGATCC[G/T]ACTGCCTCGGCCTCC | 388795 |
rs191289928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957885 | TACTGCTTTCCAGTG[A/G]TTTTTTTTTTTCTTA | 388795 |
rs191301797 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870933 | GTGCGATCTCGGCTC[A/C]CTGCAACCTCTGCCT | 388795 |
rs191301919 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917150 | GCTTAGTAAATGAGG[G/T]CAATGGGACATGGCT | 388795 |
rs191311559 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940039 | CCTTCCTTCCTTCCT[C/T]CCTTCCTTCCTTCCT | 388795 |
rs191359975 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898263 | AAGATTTCAAATGAA[A/G]GTAGGCTTGTGTGCT | 388795 |
rs191366291 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879774 | ATGAGTCTTATGACC[A/G]GCTTCAGGGGAAGGT | 388795 |
rs191407504 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924021 | ATTGAGCTCTCAATA[A/T]CTGCCAGACAATGAA | 388795 |
rs191407805 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915911 | CTCCTGGCCTCAAGT[A/G]ATCCACCTGTCTCAG | 388795 |
rs191427906 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878132 | TTAGCTGGGAATTGT[A/G]GCATGCATTTGTGGT | 388795 |
rs191528567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951424 | AGCCAGACGAAAACC[C/T]GTACATATTGTATGA | 388795 |
rs191545143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934133 | ACAGGTGTGAGCCAC[C/T]GTGCCCAGCCCTTTC | 388795 |
rs191546989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913990 | ATTTGGGGAGCCTTG[C/T]CCCCATGGTGGCTCT | 388795 |
rs191564620 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923590 | TCCAGAGGTAATTAC[A/G]TTAAGACATGTGTTG | 388795 |
rs191598381 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933649 | CCACCCTCTAAGCCT[C/T]TGGTAACCATCATTC | 388795 |
rs191670747 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896850 | TCCATTCAGGGCCAG[A/T]GGAATGATGAGTTAG | 388795 |
rs191674847 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | EFCAB8 | GRCh38.p7 | 20:32961613 | GTCAGGTTCTGAGGT[C/G]CTCCGCTGTCTTCTC | 388795 |
rs191675262 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860075 | TTTGGGAAGCCAAGG[C/T]GGGCGGAAAGCACTT | 388795 |
rs191682968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894037 | AGCAGGAGGAAGTCA[C/T]TGGAGCTGTTCTGCC | 388795 |
rs191811719 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936114 | CTCAGCTCACTGCAA[C/T]CTCTGCCTCCCAGGT | 388795 |
rs191828724 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875138 | GGTCTTTTTTAGTGC[C/T]TCCCCTCCCCACACT | 388795 |
rs191971832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939526 | CTGACTTTGTGGTCC[A/G]CCTGCCTTGGCCTCT | 388795 |
rs191998754 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946817 | TCCTTCTCCTAACCC[C/T]TGGCAGCCATTGATC | 388795 |
rs192073992 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936796 | TTTGGCTAGCCAGGG[A/T]CTTTTATGATTGCAT | 388795 |
rs192094455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867372 | GTAAAAAGGGAACAA[C/T]GGTTCCCTCTCCAAA | 388795 |
rs192166002 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923762 | GGCATCTCTTCATGA[C/T]GGTGTTTACGGAGCC | 388795 |
rs192171863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903672 | AATATGTGTACTGCC[A/G]TCTGTTCTCTTTGAA | 388795 |
rs192200815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940560 | ACAAGCTACAAAAGA[A/G]AAAAACAGATAAATT | 388795 |
rs192224146 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865431 | GTCAGAGCTGGTTAG[C/G]AAGTACTTTGAATGC | 388795 |
rs192235955 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885896 | CATTAGCCCAAACAG[G/T]TGTCCCTTTAGCTGT | 388795 |
rs192273885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913453 | CGCCTTAGGGATTAC[A/G]TTTCAATATATGAAT | 388795 |
rs192299896 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950769 | GAGGGTGAAGTTTAG[C/G]AGTTACCCAAGAGAC | 388795 |
rs192315225 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886255 | CATAATACATGTGTA[C/G]TGCTTGGGGCAGGGC | 388795 |
rs192334596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889957 | AGTAAGCTGAGATCG[C/T]GCCATTGCACTCCAG | 388795 |
rs192372183 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929083 | TGAATGCAGTTTGCT[A/G]ATTTTTTTGATAATT | 388795 |
rs192375209 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861101 | TGGAAGTCAGATTCA[G/T]CCTTCTGATGTTTGG | 388795 |
rs192401966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919293 | AGTGAGAAACACCAC[C/T]GTCCCCAAACACACA | 388795 |
rs192408292 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945550 | TGAGCATTTTTATTA[C/G]GGTTACTTAGAATTC | 388795 |
rs192412810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899157 | TTGGGAAGCCGAGGT[A/G]GGTGGATCATGAGGT | 388795 |
rs192428217 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956477 | TCAGATCAAATTTTC[A/T]GATCAAATTTTCAGA | 388795 |
rs192452650 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916301 | CTTGCTCTATTGCCT[A/C]GGCTGGAGTGCAGTG | 388795 |
rs192492931 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887716 | GACCTGGCTCTGCTC[A/G]TGGCTTTCCCTGCCT | 388795 |
rs192606075 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862240 | GGCTCAAGTAATTCT[C/G]CCACCTCAGCCTCCT | 388795 |
rs192615979 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880471 | AGATGGGGTTTCACT[C/G]TGTTGGCTGGGCTGT | 388795 |
rs192617514 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928524 | ACAGGCATGAGCCAC[C/T]GCACCCAGCCAATGC | 388795 |
rs192707195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904181 | ATTTTTTTGTACAGA[C/T]GGGATCTTGCTGTGT | 388795 |
rs192708183 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933771 | ATCACCTGAGGTCAG[G/T]AGTTCAAGACCAGCC | 388795 |
rs192712517 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865909 | ATTGTACTTGTCCCA[C/G]CAAAAGACTACAGTT | 388795 |
rs192715881 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909496 | GCCTGGGGCAAGGGG[C/G]AGGCAGGGAGGGCTT | 388795 |
rs192725084 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945625 | CTGGAGATTTATTTT[C/G/T]TTCCTTTGGGCCATG | 388795 |
rs192772773 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864893 | TTGTGTAATTACAGT[G/T]TACTGGGGCTTCACA | 388795 |
rs192776822 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902896 | TGTGGTAGCAGGAGC[C/T]GGTGCTGAGTGTGTG | 388795 |
rs192862211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959078 | CTCCAGTAATTCTGG[C/T]TCATTCAAGAAAATG | 388795 |
rs192881851 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880178 | ACCCAGACCAGGCCA[C/T]GGGGAAGTCAAAGAG | 388795 |
rs192899655 | snp | A/C | 0.000442223 | 0.0148632 | missense | EFCAB8 | GRCh38.p7 | 20:32917483 | ATGCCTCTAGGAGCC[A/C]CTCGCCCTTGCAGCC | 388795 |
rs192904428 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895709 | CCTGAGTAGCTGTGA[C/T]TACAGGCACACACCA | 388795 |
rs192920701 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934678 | TGGGTTTTTCCCACC[A/T]TTCTAATGATAGTGA | 388795 |
rs192965228 | snp | C/T | 0.000460681 | 0.01517 | missense | EFCAB8 | GRCh38.p7 | 20:32885548 | GTGTTTTTAATCCAC[C/T]GGTTCAAGAAGATCG | 388795 |
rs193028697 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938204 | TAACTGAATAAAAAA[A/C]AAAAGCCATATGATT | 388795 |
rs193125293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870532 | GGGACAGGGTCTCGC[C/T]TGGTTGCCCAGGCTG | 388795 |
rs193135114 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908996 | CTGTGGAGGATGGGG[G/T]TAAGGGGGCCCACAA | 388795 |
rs193142548 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861531 | TGACATCAGGTGATC[C/T]GTCTGCCTCGGCCTC | 388795 |
rs193153944 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899078 | TAGAGTGAAGTTTTT[C/T]CTTTTCTTTTGAAAA | 388795 |
rs193162563 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952269 | GACCCTGTCTCAAAA[A/G]AAGAAAAAAAAAATC | 388795 |
rs193228612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960445 | GGACTCCTGTCTATA[A/G]CCTCCAAGCATTTCC | 388795 |
rs193288762 | snp | C/T | 0.00394476 | 0.0442359 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889436 | GCTTCCCAGCTCTGC[C/T]CTCAGCCACTGGGAG | 388795 |
rs199550861 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921197 | TTCTGATTATTTCTC[-/T]CTCCTTTTTTTTTCT | 388795 |
rs199580596 | in-del | -/C | 0.0174175 | 0.0916809 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933072 | TATTATATATGCATT[-/C]ATTAATCTCCATAAT | 388795 |
rs199582968 | in-del | -/GAAAGAAA | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948583 | AAAGAAAGAAAGAAA[-/GAAAGAAA]AGAAAGGAAAAGAAA | 388795 |
rs199586896 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926660 | TGCTATCCCTCCCCC[C/G]TCCCCCGACCCCACA | 388795 |
rs199666553 | in-del | -/AG | 0.0566069 | 0.158427 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948570 | GAAAGAAAGAAAGAA[-/AG]AGAAAGAAAGAAAAG | 388795 |
rs199670004 | in-del | -/T | 0.00636936 | 0.0560724 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859473 | CTTTTGGGTGGTCTC[-/T]GTTGGCAGCAACCAG | 388795 |
rs199678162 | in-del | -/A | 0.0209421 | 0.100162 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901329 | GCTGATGAGCTAAAT[-/A]AAAAATCACAAAAAA | 388795 |
rs199694852 | in-del | -/TCTC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921193 | CAGGTTCTGATTATT[-/TCTC]TCTCCTTTTTTTTTC | 388795 |
rs199710083 | snp | C/T | 0.0029955 | 0.0385847 | stop-gained | EFCAB8 | GRCh38.p7 | 20:32889397 | GTTGCGTCTACCAGG[C/T]AAAAGATAGGTGAGT | 388795 |
rs199875711 | in-del | -/T/TTTTTTTTC/TTTTTTTTT | 0.31645 | 0.266817 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934279 | TCCCAAATGACAGGA[-/T/TTTTTTTTC/TTTTTTTTT]TTTTTTTTCTCTTTT | 388795 |
rs199877116 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862840 | CAATATGTTGGCCAG[A/G]CTGGTCTCATTTGAA | 388795 |
rs199908444 | in-del | -/A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912445 | AAAAAAAAAAAAAAA[-/A/G]GAAGAAGAAGAAAGA | 388795 |
rs199923515 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865320 | TGTGTATGGGAGACA[A/C]ACGTGAGTAAGCACC | 388795 |
rs199937241 | snp | A/C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956960 | TTTTTTTTTTTTTCA[A/C/T]TTTTTTTCAATCTCT | 388795 |
rs199971386 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904471 | CCCAGCTAATTTTTG[-/T]TTTTTTTTGTACAGA | 388795 |
rs200141261 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958804 | GAAAATACAAAAACC[C/G]AAGTGCTTGGATGGG | 388795 |
rs200154212 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952097 | GACTCTTGTTTCTAC[-/A]AAAAAAAAATATTAA | 388795 |
rs200191926 | snp | C/T | 9.42374e-05 | 0.00686366 | missense | EFCAB8 | GRCh38.p7 | 20:32918513 | GGCGGAGCCTGGTGT[C/T]GGCTCCCCCAGTGAT | 388795 |
rs200238691 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934287 | TGACAGGATTTTTTT[C/T]CTCTTTTAAGGCTGA | 388795 |
rs200259131 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873809 | AGAGCGAGACTCTGT[-/C]CAAAAAAAAAAAAAA | 388795 |
rs200356823 | in-del | -/T | 0.14665 | 0.227637 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928894 | GTCCTTCTATTCCTA[-/T]TTTTTTTTTTTAATT | 388795 |
rs200363561 | in-del | -/AG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916043 | CCCCACTCCTGGTAC[-/AG]CAGTTTCTGTCTTTG | 388795 |
rs200405358 | in-del | -/TC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939124 | CTTTCTCTCTTTCTT[-/TC]TCTTTCTTTCTTTCT | 388795 |
rs200436868 | in-del | -/TC | 0.0174175 | 0.0916809 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895574 | TTTTCTTTCTTTCTT[-/TC]TTTTTTTTTTTTTTA | 388795 |
rs200454658 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946882 | TCATAAATGGAAACA[C/T]ACACATGTAGCTGAG | 388795 |
rs200506925 | snp | A/G | 0.00228383 | 0.033715 | missense | EFCAB8 | GRCh38.p7 | 20:32889362 | ACATGGTATGTCTGC[A/G]CAATATGAACCTCGT | 388795 |
rs200525100 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879567 | ATGACACGGGAGCCT[-/C]CTGTAGGAAATGAAG | 388795 |
rs200578991 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928254 | TATTTTTTTTTTTTT[G/T]AGACAGAGTCTTGCT | 388795 |
rs200611291 | in-del | -/CTGT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955922 | CTTATTTTTTTCATC[-/CTGT]CTGACAATCTTTACC | 388795 |
rs200733983 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956958 | CTTTTTTTTTTTTTT[C/T]ATTTTTTTTCAATCT | 388795 |
rs200785437 | in-del | -/AC | 0.02016 | 0.0983543 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859798 | TCTCATAACCACAAT[-/AC]AGTTATCAAAAGCAG | 388795 |
rs200797051 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950010 | GTCTCAAAAACAAAC[-/A]AAACAACAAAACAAC | 388795 |
rs200972138 | in-del | -/A | 0.0279526 | 0.114869 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947669 | TGAAAATGAAAATGT[-/A]ACATTTCAAAATTTA | 388795 |
rs201012349 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867180 | CCTCCTCGGCCTCCC[A/G]AAGTGCTGGGATTAT | 388795 |
rs201075962 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914901 | TAAGTTCTGCTTCCA[-/T]TTTTTTTTTCTTTAA | 388795 |
rs201116502 | in-del | -/AG/AGAAAG | 0.0103295 | 0.0711199 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948566 | GAAAGAAAGAAAGAA[-/AG/AGAAAG]AGAAAGAAAGAAAGA | 388795 |
rs201118528 | snp | C/G | 0.000829455 | 0.020348 | missense | EFCAB8 | GRCh38.p7 | 20:32918410 | CACAGGCCCAGCAGA[C/G]CCTATGTGGAGCGGG | 388795 |
rs201168382 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929502 | CTTCTCTTCCCTTCT[-/G]TTTTTTTTTTTTTTT | 388795 |
rs201220673 | in-del | -/AA | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863543 | CTTCTGCAGGACAAC[-/AA]TCCTCTCTATCAGGG | 388795 |
rs201268457 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877210 | TTTATTTCTTTCTTT[-/C]TTTTTTTTTTTTTTT | 388795 |
rs201446192 | snp | A/G | 0.000638773 | 0.01786 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32889387 | CCTCGTTGCAGTTGC[A/G]TCTACCAGGCAAAAG | 388795 |
rs201454947 | in-del | -/AC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957330 | AATTAAAAAAAAAAA[-/AC]CCAAAACTTTTCTGG | 388795 |
rs201484631 | in-del | -/T | 0.00483381 | 0.0489238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874398 | GGCTAATTTAAAAAA[-/T]TTTTTTTTGTAGATT | 388795 |
rs201493711 | in-del | -/AAAGAAAG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948525 | TAAGAAGAAAGTGAA[-/AAAGAAAG]AAAGAAAGAAAGAAA | 388795 |
rs201513355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925013 | CTGATCTCAGCCTTT[C/T]CTTAGTGGAAGAGAG | 388795 |
rs201664463 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868015 | TAATTAAAATTTTTC[-/T]TTTTTTTTTTAGAAA | 388795 |
rs201861522 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955013 | TCCTGGACATCTATC[-/C]TCCCCATGAGTAGAG | 388795 |
rs201868299 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920884 | GGGGCATCTCCAGAC[C/T]CTAGTTAGAATGCCC | 388795 |
rs201922375 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956959 | TTTTTTTTTTTTTTC[A/C]TTTTTTTTCAATCTC | 388795 |
rs201978158 | in-del | -/CTTGGG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906038 | CAGGGCAGTTCTATT[-/CTTGGG]CATTGTATGAGATGT | 388795 |
rs202039338 | in-del | -/AA | 0.0726307 | 0.176182 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869735 | ACTGCAGATGACTGT[-/AA]GTATGTTTTCATATG | 388795 |
rs202106087 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935225 | TTTTTTTTGAGATGG[A/C]GTTTTGCTCTTGTTG | 388795 |
rs202111336 | in-del | -/T/TT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895571 | TTTTTTCTTTCTTTC[-/T/TT]TTTCTTTTTTTTTTT | 388795 |
rs202139363 | in-del | -/G | 0.0726307 | 0.176182 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869734 | CTACTGCAGATGACT[-/G]TGTATGTTTTCATAT | 388795 |
rs202169173 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934029 | TTTTTTTTTTTTTTT[G/T]TAGAGATGAGGTCTA | 388795 |
rs202207831 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958144 | GAGGATCATTCAGTC[A/C]CTGCCATAGTACTCT | 388795 |
rs202208142 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885140 | TCTGCTCACCCTCTC[C/T]TGGGCAGTTTTTCCT | 388795 |
rs207477533 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945675 | TGCCTTATAACTTTA[A/T]ATTGGGATCCATGCA | 388795 |
rs367659365 | snp | A/G | 0.000437904 | 0.0147905 | missense | EFCAB8 | GRCh38.p7 | 20:32889394 | GCAGTTGCGTCTACC[A/G]GGCAAAAGATAGGTG | 388795 |
rs367685749 | snp | A/G | 0.00011753 | 0.00766492 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930377 | CAGCCCTGCTGAGCC[A/G]GGCCCTCCTCTCTTC | 388795 |
rs367688013 | snp | C/T | 0.000437904 | 0.0147905 | utr-variant-3-prime | EFCAB8 | GRCh38.p7 | 20:32961660 | CAACCAGGCCCATGG[C/T]GGTCCTGCATGTTCT | 388795 |
rs367706156 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957616 | CCTACAACCCCAGCC[C/T]CCCTGGTGCTCGGCA | 388795 |
rs367785755 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929732 | GAGTGAGGAAGCTTC[C/T]AATTTCCCCCTTCTG | 388795 |
rs367795252 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888866 | GCTGCAGTGTCCCCT[C/T]TGAGTAGGTGCAAAC | 388795 |
rs367797748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865015 | GGAAGTGATGTGATA[C/T]GCCTAAGTTAAAATA | 388795 |
rs367800767 | snp | A/T | 0.00192899 | 0.0309964 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32898549 | CCAGATGAATGTGGT[A/T]GTCTCCTGTTCAGCC | 388795 |
rs367805831 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954322 | ATGGCATAAAATAAC[A/T]GTCCAGTTTTACTCT | 388795 |
rs367810591 | snp | A/C | 9.47463e-05 | 0.00688216 | missense | EFCAB8 | GRCh38.p7 | 20:32960111 | AAGGAACGCTTGCAG[A/C]ATACCAGGTTCCTGT | 388795 |
rs367841070 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874077 | AGGCATGTGCCACCA[C/T]GCCTGGCTAATTTTT | 388795 |
rs367857496 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889177 | ACTAGACTTAGTGGT[A/G]GTGCTAGGCTCCATG | 388795 |
rs367858707 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881048 | TTCATCCCATCCATC[A/G/T]TAGTATATGAATGTC | 388795 |
rs367891283 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917100 | TTTATGTAAAGCCCC[C/T]ACAACAGGGCCTTTG | 388795 |
rs367893602 | snp | C/T | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32961479 | CCTCGGTCCCATCCC[C/T]GGTGTCCAAGTCCAC | 388795 |
rs367935823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892983 | GTAGCTGGGATTACT[A/G]GTGCCCGCCACCACG | 388795 |
rs367945984 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901549 | AGGGCCTCTGTGGGC[C/T]GGGCCTGCTGCCTTC | 388795 |
rs367959987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870741 | TCCTGGCTTCAAGCA[A/G]TCCTTCTGCCTCTGC | 388795 |
rs368072032 | in-del | -/AAT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899229 | CTCTACTAAAAATAC[-/AAT]AATAATAATAATAAT | 388795 |
rs368098613 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929203 | GCTGGCCTCATAGAA[C/T]GAGTTAGGAAGTGTT | 388795 |
rs368132965 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893417 | GGAGTCTCTGGGAAG[A/G]CGTCTGCTTCCAAGC | 388795 |
rs368146512 | in-del | -/CTTTC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895571 | CTTTTTTCTTTCTTT[-/CTTTC]TTTTTTTTTTTTTTA | 388795 |
rs368308316 | snp | A/C/T | 0.000360767 | 0.0134267 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912906 | AGGTTCCAGTAGCTG[A/C/T]GTGTTCTCTCTCCAG | 388795 |
rs368326053 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911442 | GGGAGTGGAGGCCCC[A/G]GCCTCTCCAGCAGCC | 388795 |
rs368402091 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886645 | CTTCCATAGCCATCC[A/G]CCTTACCTTTCTGTG | 388795 |
rs368404552 | in-del | -/TAGT | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886196 | TCTGTCAAATGGGGC[-/TAGT]TACAGTGCTTCTTTA | 388795 |
rs368430062 | snp | A/G | 0.00449142 | 0.0471756 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898653 | TCTCCTGGCTAAGGC[A/G]GTGGGGCTGGAAGGG | 388795 |
rs368442281 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913203 | ATAAACAACATAAAT[G/T]TATTTATCAGAGTTC | 388795 |
rs368454048 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930231 | ATAGTCGAGTATGAC[A/G]TTCCTTGTCACCAGC | 388795 |
rs368469619 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901688 | TTATTGATTGACTGA[C/T]TGATTGATTGATTGA | 388795 |
rs368511692 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926743 | TCAATTCCCACCTAT[A/G]AGTGAGAATATGCGG | 388795 |
rs368529658 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947919 | AAAAAAAAAAAAAAA[-/G]AAAAAAGAAACTAGA | 388795 |
rs368538403 | snp | C/T | 8.93296e-05 | 0.00668258 | missense | EFCAB8 | GRCh38.p7 | 20:32896499 | TCTTAAATGAGAAGT[C/T]TGCTTTGCATAGAAG | 388795 |
rs368542932 | snp | A/G | 0.00173904 | 0.0294363 | missense | EFCAB8 | GRCh38.p7 | 20:32959920 | ATGTCCCCGTGGGCC[A/G]GAGAGCGCCCCCTGG | 388795 |
rs368555385 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935327 | CGCCTCAGCCTCCTG[A/T]GTAGCTGTGATTACA | 388795 |
rs368558017 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896851 | CCATTCAGGGCCAGA[A/G]GAATGATGAGTTAGA | 388795 |
rs368562159 | snp | A/G | 0.000183234 | 0.00956993 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32889354 | GGTCATTGACATGGT[A/G]TGTCTGCACAATATG | 388795 |
rs368574521 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862204 | GGTATGATCTCAGCT[C/T]TCTGCAGCCTCAACC | 388795 |
rs368633916 | snp | C/G | 0.00128842 | 0.0253486 | missense | EFCAB8 | GRCh38.p7 | 20:32920085 | CTTTCCAGAAACCTT[C/G]CAGTGCTTCTGGCAC | 388795 |
rs368636804 | in-del | -/AATA | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859746 | GCCCTTTTACCCCTA[-/AATA]CTTTTCAGTGTACAT | 388795 |
rs368695192 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915570 | TTCTCTGCATCTGTC[A/C]TCTTTTCTTTCTAGG | 388795 |
rs368726721 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917706 | AAAATGGAGGCACAC[A/G]GAGATGAAGCACCTT | 388795 |
rs368801244 | snp | A/G | 0.000875616 | 0.0209055 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943848 | CCCATGGCCCTTCTT[A/G]TCTCTGTCCCTGTCT | 388795 |
rs368849174 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877967 | TGCGAGTAGGCCCTT[C/G]CCATACTCAGGATTC | 388795 |
rs368854813 | snp | A/G | 9.70356e-05 | 0.00696479 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863874 | AATAAAGGGTGGGGC[A/G]TTCCAGAGTCACCCA | 388795 |
rs368889672 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919977 | TACCTACTGCGGGGG[C/T]TTGGGAGTGCCGCTC | 388795 |
rs368895344 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923035 | AAAAAATTAAAAAAA[-/A]TTAGCCAGGTTTGAT | 388795 |
rs368902836 | snp | C/T | 0.000369276 | 0.0135831 | missense | EFCAB8 | GRCh38.p7 | 20:32867709 | TACACCTGGCCAAGA[C/T]AGAGAAAATGTTTGA | 388795 |
rs368906881 | in-del | -/T | 0.38821 | 0.208322 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891828 | GTTGGAAGGAGTCAG[-/T]TTTTTTTTTTTTTTA | 388795 |
rs368916672 | in-del | -/GTTT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944284 | TTTGTTTGTTTGTTT[-/GTTT]TAGTGACCTGTCTCT | 388795 |
rs368943512 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942980 | TGTTTAAAATTTAAA[A/G]TTTATTATTCTGACT | 388795 |
rs368971174 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894646 | GGTATGTACCCCAGC[C/T]CTGTGTGACCTGGAG | 388795 |
rs368982936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861357 | GCAATGGCACAATCT[C/T]GGCTCACCGCAACCT | 388795 |
rs369016469 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875483 | TGCCTTGAACTGAGC[A/G]CACCTGGTAAACATG | 388795 |
rs369045475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891371 | TACAGGTGCGCGCTA[C/T]CACACCCAGCAAATT | 388795 |
rs369057961 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884521 | GATAGGAGAGAGGAG[A/G]ACCGTGTCCAGACAC | 388795 |
rs369072708 | snp | A/G | 0.000875616 | 0.0209055 | missense | EFCAB8 | GRCh38.p7 | 20:32961431 | TCTCCTTCTTGCTGC[A/G]GCCCCAGTCAGCCTC | 388795 |
rs369094669 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939387 | TCCCAGGTTCAAACG[A/G]TTTTCCTGCCTCAGC | 388795 |
rs369120371 | snp | A/T | 0.0030613 | 0.0390036 | missense | EFCAB8 | GRCh38.p7 | 20:32906942 | CCTCAGTGACGCACA[A/T]CCTTGTGGATAGCAG | 388795 |
rs369133956 | in-del | -/A/AA | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873809 | GAGCGAGACTCTGTC[-/A/AA]CAAAAAAAAAAAAAA | 388795 |
rs369164357 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931947 | TCAGACCCAGAAGAA[C/T]ATATATTAGAAATGA | 388795 |
rs369174343 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951572 | ATGAGGGTTGGAAGG[A/G]TGGGAGCTCAAAGAA | 388795 |
rs369239297 | snp | A/G | 0.000437904 | 0.0147905 | missense | EFCAB8 | GRCh38.p7 | 20:32917374 | GACATCCTGAGCATG[A/G]CCAAGTACCGGAACC | 388795 |
rs369266123 | snp | G/T | 9.25712e-05 | 0.00680272 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892176 | GACCTCCCAGGCATG[G/T]CTGTGGGCTCTATGT | 388795 |
rs369276263 | snp | A/G | 0.000437904 | 0.0147905 | missense | EFCAB8 | GRCh38.p7 | 20:32930521 | CTGGGGAAGTTCCCT[A/G]TGGACCTAGACAATG | 388795 |
rs369325297 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888788 | GTCTGGGTGGTGTCC[A/G]TGGTGTGGGTTGATA | 388795 |
rs369336389 | snp | G/T | 0.00175047 | 0.0295325 | missense | EFCAB8 | GRCh38.p7 | 20:32911565 | TTGCTGTGTCTGGGG[G/T]CCAGCACGTGGAGAT | 388795 |
rs369342169 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889831 | ACATGGTGAAACCCC[A/G]CCTCTACTAAAAATA | 388795 |
rs369394983 | in-del | -/TTCT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939066 | TCTTTCTTTCTTTCT[-/TTCT]CTCTCCCCAACTTCT | 388795 |
rs369443493 | snp | A/G | 0.000354453 | 0.0133079 | missense | EFCAB8 | GRCh38.p7 | 20:32875985 | AGCAGTGTGTCGGAC[A/G]AGATGCTAAAGGAGC | 388795 |
rs369559496 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946511 | CTCCATAGGGAGAAG[A/G]AAGTTCTGGATCTTC | 388795 |
rs369578508 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899122 | CGGGCGCGGTGGCTC[A/G]CGCCAGTAATCCCAG | 388795 |
rs369666933 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949955 | CAGTGAGCCAAGATC[G/T]CACCACTGCACTGCA | 388795 |
rs369683615 | in-del | -/GATGGCAGGAGGATATCAGGGGGTCACCTCACCAGGGCCAGGAGGGCCTCTGTGGGCCGGGCCTGCTGCCT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901492 | GTTTTATTGAGTCCT[lengthTooLong]TCCTGACCTCATTGC | 388795 |
rs369684827 | snp | A/G | 0.000437904 | 0.0147905 | missense | EFCAB8 | GRCh38.p7 | 20:32892272 | TTTGTTGATCTGGAC[A/G]GCTGTGCTCTGGTCA | 388795 |
rs369693770 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924925 | AGGGTCCCTTCTCTC[C/T]GGGGCACTTGTGGGC | 388795 |
rs369740305 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877207 | TTTATTTATTTCTTT[C/T]TTTTTTTTTTTTTTT | 388795 |
rs369750491 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908691 | GGAGCCACCCTGAAC[A/G]TCAGGCTTGTTAGGA | 388795 |
rs369755895 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946112 | CTCATTCCACAGAGC[A/G]GCAGGAGGGACTCTG | 388795 |
rs369876818 | snp | C/G | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32943737 | GTATGTGGACAACTT[C/G]CAGCTGGTTATCAGC | 388795 |
rs369915968 | snp | C/T | 0.00597247 | 0.0543191 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860153 | TTTCTACTAAAAATA[C/T]GAAAGTTAGCTGGGC | 388795 |
rs369917049 | snp | A/G | 0.000507382 | 0.0159196 | missense | EFCAB8 | GRCh38.p7 | 20:32906857 | GTGACTGGTGGCTAC[A/G]ATGCCTTCATCCGCC | 388795 |
rs369921062 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921831 | TTTTGTTACCTTATT[C/T]TTTTTTTTTTTTTTT | 388795 |
rs369944682 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902219 | GCTTATATGTTGCAG[A/G]TGGAGTGTCCATGGG | 388795 |
rs369947351 | snp | A/G | 9.23063e-05 | 0.00679298 | splice-acceptor-variant | EFCAB8 | GRCh38.p7 | 20:32918360 | CTTTCTTCTTGGTAC[A/G]GGTGCAAGATGTGAA | 388795 |
rs369986842 | in-del | -/TTTTCTTTCTTTTC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929419 | GGATAATTGAGATTT[-/TTTTCTTTCTTTTC]TTTTCTTTCTTTTCT | 388795 |
rs370020426 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935655 | GGGATTACAGGCATG[C/T]GCCACCACGCCCAAC | 388795 |
rs370025993 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950487 | AACCTGAGAGGGGCG[G/T]CTGGCTGAGTTAGGT | 388795 |
rs370130900 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928278 | TCTTGCTCTGTCGCC[C/T]AGGCTGGAGTACAAT | 388795 |
rs370131515 | in-del | -/CT/TC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922814 | TCTCTCTCTCTCTCT[-/CT/TC]GTATCTCTCTCTGAT | 388795 |
rs370143601 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896184 | CAGCACCTAGGAAGC[A/G]TGAGGTGCCCTGAAA | 388795 |
rs370178736 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861686 | GGAGGATCACCTGAG[A/C]CCAGGAGTGCAAAAC | 388795 |
rs370184509 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960983 | TGGGCCCGCAGGCCA[C/T]GGTGGTTAGTGGTAG | 388795 |
rs370194344 | snp | A/G | 0.00095229 | 0.0218 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960050 | CCTTCATTCTTGGGC[A/G]TGGCTCCTGCAGGTG | 388795 |
rs370300511 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884259 | GAGCCTGGGCCGGGT[A/G]CACCAAATGCAGCCT | 388795 |
rs370315093 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905099 | CTCTGAGCCTCACCC[A/G]GCCCTAATGAGCCTC | 388795 |
rs370321314 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925567 | CATGTTGTCCAGGCT[C/T]GTCTCGAACTCCTGG | 388795 |
rs370329065 | snp | C/T | 0.000437904 | 0.0147905 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32908283 | CCCCCAGAATATTCG[C/T]GTGTGGGACATGCTG | 388795 |
rs370371285 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935304 | CTCCCGGGTTCAAGC[A/G]ATTCTCCCGCCTCAG | 388795 |
rs370382704 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910883 | GCTGGGACTACAGGC[A/C]TGCACCACCACCCCC | 388795 |
rs370399392 | snp | A/G | 0.000999357 | 0.0223311 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32959832 | GCGAGAGCAGGCGGC[A/G]CTGATGGCTCTCCTG | 388795 |
rs370447821 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947053 | TAGGACATTTGAGTC[A/G]TTGTCAGTTTTGGAT | 388795 |
rs370450264 | in-del | -/AAAG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948525 | TAAGAAGAAAGTGAA[-/AAAG]AAAGAAAGAAAGAAA | 388795 |
rs370502473 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941697 | GTGGTTTCCTGAGGC[C/T]GGGGGAGGGAGTTGG | 388795 |
rs370521640 | in-del | -/ACAAAA | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872809 | AAAACAAAAACAAAA[-/ACAAAA]GGCCGGGTGCAGTGG | 388795 |
rs370573985 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895981 | GACATGCTTATTTTA[C/T]GATGCATGCCTGGAA | 388795 |
rs370619833 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954086 | GCTGGGATCTTAGAT[G/T]TGAGCCACCACACCC | 388795 |
rs370640614 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914881 | TATGGATAGGATGAA[C/T]CTTTTAAGTTCTGCT | 388795 |
rs370648654 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932813 | GAAGTGGGATTGCTA[A/G]GTAAAAGGGTTACAT | 388795 |
rs370655009 | snp | A/G | 9.579e-05 | 0.00691996 | missense | EFCAB8 | GRCh38.p7 | 20:32918531 | CTCCCCCAGTGATGC[A/G]GTGCCCGAGAGACAA | 388795 |
rs370662541 | snp | A/G | 0.000437904 | 0.0147905 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32961480 | CTCGGTCCCATCCCC[A/G]GTGTCCAAGTCCACC | 388795 |
rs370679729 | in-del | -/CAA | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950037 | CAACAACAACAACAA[-/CAA]AAATGGAACATAGAA | 388795 |
rs370686940 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888081 | CTTTCTTTTTTTTTT[-/T]GAGACTGGGTCTTGC | 388795 |
rs370750590 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862437 | CATTAAAACCACTTT[-/C]CCTCTTTGCTCCTTT | 388795 |
rs370753215 | snp | A/G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863403 | CCCTCATTTTTCTAA[A/G/T]CTGTTTATTGTACTT | 388795 |
rs370764882 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893341 | GAGGCCTGGGCATGG[C/T]CTAGATGTGGGTGCT | 388795 |
rs370770406 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910714 | TCAGTAGGGAGGGTT[A/G]GTCTGAAACCACCTC | 388795 |
rs370777605 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929303 | AATTCACTGGTGAAG[A/C]CATCAAGCTTTGGGC | 388795 |
rs370787612 | snp | A/G | 9.69321e-05 | 0.00696108 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867545 | GGCTCAGGAAATTGA[A/G]ACGCTCAGTCCCTGG | 388795 |
rs370788167 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906203 | TGCCTGTCCCAGTAC[A/G]GTTGATGTGAAAATC | 388795 |
rs370808435 | snp | A/G | 0.000182732 | 0.00955681 | missense | EFCAB8 | GRCh38.p7 | 20:32893272 | GGCTGTTCAACCCCC[A/G]TATCCTCCCCAGGGC | 388795 |
rs370838570 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955496 | AGTGAGTTAAGACTG[C/T]GCTGCTGTACTCCAG | 388795 |
rs370858830 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915463 | TTTCTCATTTCTTCA[A/C/T]CAGAGACTTCACCAG | 388795 |
rs370895375 | snp | C/T | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859740 | CATCATGCCCTTTTA[C/T]CCCTAAATACTTTTC | 388795 |
rs370907602 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958965 | TTGTGTTATTTCCCT[G/T]ATTTGCAGGGAGGAG | 388795 |
rs370918928 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884949 | AGGGCGGCCTCCTGC[A/G]AGGCCAGGCCTGCCC | 388795 |
rs370955049 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909175 | GTGTGTCATCCTTAC[A/G]CACTTGGCTGGCCCT | 388795 |
rs370968452 | in-del | -/TT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895314 | TTATTTTATTTAAGA[-/TT]TTTTTTTTTTTTTTT | 388795 |
rs371023833 | in-del | -/TTG | 0.00517822 | 0.0506191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926413 | GAACGTTTGAAACTA[-/TTG]TTTATTTAGCTGTTT | 388795 |
rs371052107 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957297 | TTGGCCTTTTCACAT[A/G]TCATATATACAAAAT | 388795 |
rs371107846 | snp | A/C | 0.00119737 | 0.0244387 | missense | EFCAB8 | GRCh38.p7 | 20:32911592 | AGATGACCGCCATGG[A/C]CCTGGATGAGTCAGA | 388795 |
rs371211466 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908240 | TACATCCCCGAGACC[C/T]ATGCTCAGCGTCTTG | 388795 |
rs371235668 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900168 | AGAGGGCCATTTAGA[C/T]CCATGTCTGTCCCTT | 388795 |
rs371262047 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873029 | ACCCAGGATGCGGAG[A/G]TTGCAGTGAGCCGAG | 388795 |
rs371300323 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945241 | TCAGCTCACTGAAGC[C/T]TTGACCTCCCAGCCT | 388795 |
rs371307201 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894232 | ACCCCCTCTTCCAGC[A/C]AGAGTTACTAAGCAG | 388795 |
rs371324438 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867547 | CTCAGGAAATTGAAA[C/T]GCTCAGTCCCTGGTT | 388795 |
rs371330684 | in-del | -/G | 0.00993419 | 0.0697739 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887500 | GAATCACTGGAACCC[-/G]GGAGGCAGAGGTTCC | 388795 |
rs371333423 | snp | A/G | 0.000437904 | 0.0147905 | missense | EFCAB8 | GRCh38.p7 | 20:32959891 | CTTGGGCCAAGCTGC[A/G]GAAGATGGCCCTGAT | 388795 |
rs371419521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888632 | AAGTGCTGAGATTAC[A/G]GGCGTGAGCCACTGT | 388795 |
rs371469092 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886592 | GGCTCTCCTTGGTGC[A/C]CCAAGGGGGAGTCAC | 388795 |
rs371521530 | snp | A/G | 0.000896459 | 0.0211524 | missense | EFCAB8 | GRCh38.p7 | 20:32896520 | TGCATAGAAGCTACC[A/G]GCTGAAGGTGAGTTT | 388795 |
rs371550925 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875173 | TGGGACCAACACAGT[G/T]CTCCCATATGGCGGG | 388795 |
rs371652732 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871495 | ATGCTGTATTCCTTG[A/C]TTTTTTAAAAAATTA | 388795 |
rs371746879 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919256 | TCAAAATCTGATTTC[A/C]ATTCCTGGGAGCTGA | 388795 |
rs371768620 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943974 | ATCCATTCAGCAAAC[A/G]GTCCATCCATTCACC | 388795 |
rs371803318 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908194 | CCTGGCCTTGTTCGC[C/T]GGAGGCACCCCCGAG | 388795 |
rs371815032 | in-del | -/TAA | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869733 | CTACTGCAGATGACT[-/TAA]GTGTATGTTTTCATA | 388795 |
rs371819020 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860708 | AAATTGGCATCATAG[C/T]GTGCACCCTTTTCTG | 388795 |
rs371834145 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907004 | GACAAGGTCCGCCCC[A/G]ACGGTCCGCCTGACT | 388795 |
rs371854292 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878565 | GCCCAGGTCGGACTG[C/T]GGACTGCAGTGGCGC | 388795 |
rs371881608 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948610 | GAAAGCAAACTATCA[A/G]TTAATATCCCTCATA | 388795 |
rs371885172 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923650 | CAAGTACATACATGT[A/G]TGAATGTATATATAT | 388795 |
rs371895986 | snp | C/G | 9.22382e-05 | 0.00679048 | missense | EFCAB8 | GRCh38.p7 | 20:32892217 | CTTTCCCCCAGATTT[C/G]TTTGATATTAGTGAC | 388795 |
rs371942367 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939014 | TCCCTCCTTCCCTCC[C/T]TCCCTCCCTCCCTCC | 388795 |
rs371942920 | snp | A/G | 0.000180213 | 0.00949072 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912907 | GGTTCCAGTAGCTGC[A/G]TGTTCTCTCTCCAGA | 388795 |
rs371955159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863175 | TGCCCTCTGGACTCT[C/T]GCCTGGTGGGACTTG | 388795 |
rs371985489 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954355 | TGCATGTGGCAATTC[A/G]GTTTTCCCAAAACCA | 388795 |
rs371990953 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862658 | TTGGGACAGAGTCTT[A/G]CTCTTGTTGCCCAGG | 388795 |
rs372015818 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895301 | AGACAGGCTTGTTTT[A/T]TTTTATTTAAGATTT | 388795 |
rs372019409 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889186 | AGTGGTAGTGCTAGG[C/T]TCCATGCCAGGTCTG | 388795 |
rs372026942 | snp | A/G | 0.000184179 | 0.00959456 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32906571 | TTGTAGGTTGTCAGT[A/G]CTGCGTTTAAGGAAA | 388795 |
rs372027781 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912741 | GACATTTAGGGCCCA[C/G]AGCCATTTTCTCTGA | 388795 |
rs372028720 | snp | A/G | 0.00511646 | 0.0503195 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32898597 | GGTGCTGACAATATT[A/G]CCAGCCAAAGCCTCT | 388795 |
rs372037700 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930667 | TGCCAGCTAAGTGTT[C/T]GGCCATCTCTTTGCT | 388795 |
rs372068414 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891147 | GACAGTCTCACTCTG[-/T]CACCCAGGCTGGAGT | 388795 |
rs372096820 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898785 | TGAGAACACAGCAGC[-/C]TCTTTTATCTCCCAA | 388795 |
rs372153975 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917238 | AAGGCTCCAGTGCTT[C/T]CCCAATGGATGGAGC | 388795 |
rs372169789 | snp | A/G | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32911499 | TGAGTGGCTGCCTGC[A/G]CGGCACAGTGAGTGT | 388795 |
rs372198138 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907252 | CTCAGTCCTCAGTCT[C/T]CCTATCCATAGAATG | 388795 |
rs372201814 | snp | C/T | 0.109108 | 0.206518 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926756 | ATGAGTGAGAATATG[C/T]GGTGTTTGGTTTTTT | 388795 |
rs372214136 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892133 | GAGATTCCTTGGGAT[A/G]GCAATGAGGCTGCTC | 388795 |
rs372230429 | snp | A/C | 9.20768e-05 | 0.00678454 | missense | EFCAB8 | GRCh38.p7 | 20:32920130 | GCAAGATCCACAGCA[A/C]ACAGTCCATTTACAA | 388795 |
rs372246126 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929518 | TTTTTTTTTTTTTTT[C/T]TTTAAATAGAGATAG | 388795 |
rs372251417 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902448 | TGTCTTCAAAAAAAA[-/A]CAAAAGACTCCATTC | 388795 |
rs372277609 | snp | C/G | 9.61955e-05 | 0.00693459 | missense | EFCAB8 | GRCh38.p7 | 20:32918535 | CCCAGTGATGCGGTG[C/G]CCGAGAGACAAGGAG | 388795 |
rs372280286 | snp | A/C | 0.000437904 | 0.0147905 | missense | EFCAB8 | GRCh38.p7 | 20:32930604 | CACGGGGGATTGTAA[A/C]GGATACATCAAGGTG | 388795 |
rs372307921 | in-del | -/GGTGTTTT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920923 | CTGGAAGGGTGTTTT[-/GGTGTTTT]ATACCGAACACGAGT | 388795 |
rs372375448 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885423 | TTGTCCCTCCTCCTC[A/G]GTGGCTCTCTGTTCT | 388795 |
rs372382285 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867944 | CATGCTCAAGCGATC[C/T]TCCTGTCTCAGCCCC | 388795 |
rs372385790 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913319 | CTTACTGTAAACTTA[C/T]ATGGTGGAAGGGTTA | 388795 |
rs372386951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884525 | GGAGAGAGGAGAACC[A/G]TGTCCAGACACGTTT | 388795 |
rs372429065 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912639 | GGGAATAGGATGTGA[C/G]AACATGATGACAAAT | 388795 |
rs372430645 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935191 | CTTTCTTTCTTTCTT[C/T]CTTTTTTTTTTTTTT | 388795 |
rs372444226 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881899 | TTTTAAAACATGGTG[A/G]CTGTTTCTTGCTTAG | 388795 |
rs372464707 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863994 | TGTATTTTTTTTTTT[-/T]GAGACAGAGTCTCGC | 388795 |
rs372471270 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895857 | ATTACAGGCGTGAGC[C/T]ACCGTGCCTGGCCCA | 388795 |
rs372490413 | in-del | -/TG | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943229 | GCTTAGGCTAGTTAT[-/TG]AACATGTCTGACTCT | 388795 |
rs372541676 | snp | A/G | 0.000179324 | 0.0094673 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878854 | GGGGTGACTGGACAA[A/G]TGCTGGTGCCAGCCT | 388795 |
rs372610658 | snp | A/G | 0.000437904 | 0.0147905 | missense | EFCAB8 | GRCh38.p7 | 20:32911502 | GTGGCTGCCTGCGCG[A/G]CACAGTGAGTGTGTG | 388795 |
rs372841373 | snp | A/G | 0.000437904 | 0.0147905 | missense | EFCAB8 | GRCh38.p7 | 20:32961460 | TCCACAGCCCATTCC[A/G]CCCCCTCGGTCCCAT | 388795 |
rs372872169 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893921 | AGGTCACCTGTACAC[A/G/T]CCCCTGCCTGGTGAG | 388795 |
rs372892250 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938209 | GAATAAAAAACAAAA[A/G]CCATATGATTATGCC | 388795 |
rs372927011 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871320 | CCTGTGTAGCCCAGG[A/G]TGGAGTGCAGTGGTG | 388795 |
rs372955771 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914176 | ATGCTGTACCATGGT[C/T]CACAGGAGCCACACC | 388795 |
rs372965478 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950639 | CTGTTCCCATACATC[C/T]TTCTGCAGCTGCAGG | 388795 |
rs372994015 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908831 | GGAAACAGGGGCCAC[A/G]TCCGAGCAGCATCTC | 388795 |
rs373060713 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940749 | ACCAAATTAAGATAC[A/G]GGTAAAGGATCTAAA | 388795 |
rs373168939 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892598 | GACATCACAGTCTAT[A/T]GCGAGGGGTGACTTA | 388795 |
rs373317696 | snp | A/C | 0.0021876 | 0.0330002 | missense | EFCAB8 | GRCh38.p7 | 20:32906991 | CAGTGTCTCCAAGGA[A/C]AAGGTCCGCCCCGAC | 388795 |
rs373327126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876670 | GGGGTAGGTGCTATT[A/G]CTTACCTCTATTTCG | 388795 |
rs373402155 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933615 | ATAACTTCCCATTCT[C/G]TCTCCCTTATTCCCC | 388795 |
rs373402663 | snp | A/G | 0.000204436 | 0.0101082 | missense | EFCAB8 | GRCh38.p7 | 20:32959927 | CGTGGGCCGGAGAGC[A/G]CCCCCTGGAAGACAT | 388795 |
rs373411849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919825 | TTTTAACCAGGATGG[C/T]CTCTTCCAGGACAAA | 388795 |
rs373412972 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887059 | TGGTCCATTGTCTTC[A/C]CCGCCAGAACCACCT | 388795 |
rs373425642 | snp | C/T | 0.000992415 | 0.0222536 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32959833 | CGAGAGCAGGCGGCG[C/T]TGATGGCTCTCCTGC | 388795 |
rs373463144 | snp | A/G | 0.000303475 | 0.0123144 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867769 | CCGCTCTGTAGGCTC[A/G]GTTTTTGTGTGAGTT | 388795 |
rs373501957 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887982 | TTCCTTCCCTGAGTT[C/T]CTACTTCCTCTCCCT | 388795 |
rs373535629 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32961318 | TACCACGGACAGCAC[A/G]CCTGCGGCCGCCTCC | 388795 |
rs373552282 | in-del | -/AA | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948561 | AAGAAAGAAAGAAAG[-/AA]AGAAAGAAAGAAAGA | 388795 |
rs373586132 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887636 | CTCATCTCTGGTTCC[A/T]CTCCAACTCTAAGCC | 388795 |
rs373617755 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869264 | TTTTTTGAGACGGAG[C/T]TTCACTCTTGTTGCC | 388795 |
rs373640511 | snp | C/G | 0.000437904 | 0.0147905 | missense | EFCAB8 | GRCh38.p7 | 20:32875997 | GACGAGATGCTAAAG[C/G]AGCTGTTTTTGAAGG | 388795 |
rs373658242 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946113 | TCATTCCACAGAGCG[C/G]CAGGAGGGACTCTGA | 388795 |
rs373695571 | snp | C/T | 0.000798403 | 0.0199641 | missense | EFCAB8 | GRCh38.p7 | 20:32961541 | GTCTCCTCCTTCGAG[C/T]GGCCCCCAAGGCCTC | 388795 |
rs373754312 | snp | A/G | 0.00155046 | 0.0277997 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912755 | AGAGCCATTTTCTCT[A/G]ATAAGTTTTCTAGTT | 388795 |
rs373800243 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935908 | TGTATGATTTACATA[-/T]ATTTTCTGTCACTCT | 388795 |
rs373887473 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946719 | GTTTCATGAATGCAT[A/G]CAATTGTGTAATTGG | 388795 |
rs373893714 | snp | A/G | 9.22552e-05 | 0.0067911 | missense | EFCAB8 | GRCh38.p7 | 20:32918438 | GGGAGAAGTGGACAT[A/G]CAAGACCTCCAGGAA | 388795 |
rs373905843 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899183 | GAGGTCAGGAGATCG[A/C]GACCATCCTGGCTAA | 388795 |
rs373928266 | in-del | -/AGAAAAAGAGTTA | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931763 | ACTTCGTTTCAAAAA[-/AGAAAAAGAGTTA]GTATTCGTAATAATG | 388795 |
rs373987449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892936 | GCCTCCACCTGCCGG[A/G]TTCAAGTGATTCTCC | 388795 |
rs373987935 | snp | A/G | 0.00175447 | 0.0295661 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32885598 | CAAAGACGGGATCCT[A/G]CAGTTCTGGTCTGAG | 388795 |
rs373994818 | in-del | -/TCTT | 0.165139 | 0.235157 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939052 | CTTCCTTCGTTTCTC[-/TCTT]TCTTTCTTTCTCTCT | 388795 |
rs374008340 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866516 | ATGAGGCCTGGAGGG[G/T]TGGGGAAGGCTTCTG | 388795 |
rs374011117 | snp | A/C/G | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860183 | CATGGTGGCGTGCAC[A/C/G]TATAATCCCAGCTAC | 388795 |
rs374029949 | snp | C/G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925054 | GCTGGGGTAAGGACA[C/G/T]CAGACAGGGAGTGGG | 388795 |
rs374033189 | snp | G/T | 0.000437904 | 0.0147905 | missense | EFCAB8 | GRCh38.p7 | 20:32918400 | GGCTGAGAGCCACAG[G/T]CCCAGCAGACCCTAT | 388795 |
rs374054340 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948693 | ATCACATAGGGTTTA[C/T]CCCAGATATACAAGG | 388795 |
rs374084116 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912879 | TGTGAGTAGAAAGCA[C/T]GTATGGTGAGTAGGT | 388795 |
rs374087473 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894820 | TCCCTCACAGCCTAG[C/T]AGGAGAGACAGGCAG | 388795 |
rs374090284 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910255 | CAGAGTGCTAGTTGT[A/G]GGGCGCTTTCCTAGG | 388795 |
rs374092621 | snp | A/G | 0.000823158 | 0.0202707 | missense | EFCAB8 | GRCh38.p7 | 20:32893274 | CTGTTCAACCCCCGT[A/G]TCCTCCCCAGGGCCT | 388795 |
rs374098246 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863061 | CCTCCCCTCTGCCTC[C/T]AGGACCCTTCAGATC | 388795 |
rs374101436 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860631 | CGTGCCTCAGTCTCC[C/T]GAGTAGCTGGGATTA | 388795 |
rs374142164 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953987 | ATTTTTGTATTTTTA[A/G]TAGAGACAGAGTTTC | 388795 |
rs374169216 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881843 | AGATGGGATGAAGGC[A/G]CAATCCACCCCCATC | 388795 |
rs374173714 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943480 | ACCTATGTAAGGTCG[C/T]AAGCAAGTTCATGTG | 388795 |
rs374190799 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906341 | TTGGGGCCAGGACTG[A/G]GCTGCTGCTTTGCCT | 388795 |
rs374203583 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907011 | TCCGCCCCGACGGTC[C/T]GCCTGACTCCTTCTG | 388795 |
rs374205136 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873040 | GGAGGTTGCAGTGAG[C/G]CGAGATCGTGCCATT | 388795 |
rs374369433 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880635 | AAATATGAATGATAA[A/G]AGATTTCATAACTGT | 388795 |
rs374379192 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928719 | CTTTTTTTGCCTAAT[C/T]CCTCTGGCAGAACTT | 388795 |
rs374403132 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929589 | TCAAGTGATTCACCC[A/G]CCTCGGCCTCCCAAA | 388795 |
rs374412560 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942243 | CAAATGGTTTCTTTT[G/T]ATTTTAATTAAGATG | 388795 |
rs374428388 | snp | G/T | 0.000276944 | 0.0117642 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32911617 | GTCAGAGCGGTGCCT[G/T]CTCACAGGTTTGCGG | 388795 |
rs374444517 | snp | C/T | 0.000102401 | 0.00715473 | missense | EFCAB8 | GRCh38.p7 | 20:32959914 | GCCCTGATGTCCCCG[C/T]GGGCCGGAGAGCGCC | 388795 |
rs374491692 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916896 | TGCAATCTGAAGCGT[A/G]AGAAGGAAGGGTCTC | 388795 |
rs374503285 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954975 | TATGGCCAGGAACCA[C/T]TGAGTGCCCAAAACC | 388795 |
rs374509351 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922841 | TCTGTATCTCTCTCT[C/G]ATACTTTCTTCCTCT | 388795 |
rs374519881 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885112 | TTTCTCAGTTTTCAG[C/G]CTCAGGCTCCACTCT | 388795 |
rs374580855 | snp | C/G/T | 0.000437904 | 0.0147905 | missense, synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32908376 | CAGTGCCTACTTCTT[C/G/T]GAGAAGGACAATACC | 388795 |
rs374611635 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877195 | AATTTTCTTGTTTTT[A/G]TTTATTTCTTTCTTT | 388795 |
rs374653923 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906490 | AGCTCCTCCCACCCC[A/G]GGCTCAGTCTCAGAC | 388795 |
rs374677422 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935314 | CAAGCAATTCTCCCG[A/C]CTCAGCCTCCTGAGT | 388795 |
rs374694452 | snp | C/T | 0.000437904 | 0.0147905 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32961327 | CAGCACGCCTGCGGC[C/T]GCCTCCTCCCCATCT | 388795 |
rs374695806 | snp | C/T | 0.00318978 | 0.0398085 | downstream-variant-500B | EFCAB8 | GRCh38.p7 | 20:32962168 | CTGCCGCTGTCAGGC[C/T]ATGGAGTCCCATGTG | 388795 |
rs374702817 | snp | A/C | | | utr-variant-3-prime | EFCAB8 | GRCh38.p7 | 20:32961725 | TCTTCCCCCGGCCAC[A/C]CCACTGGGCCTCTCT | 388795 |
rs374705413 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905359 | CCTGTGTAGTTTCAT[A/G]TGAAGTTTGATGAAG | 388795 |
rs374736025 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954112 | CACCCAGCATGATTA[C/T]GTTTTTTGATACACA | 388795 |
rs374743434 | snp | C/T | 9.12784e-05 | 0.00675506 | missense | EFCAB8 | GRCh38.p7 | 20:32889386 | ACCTCGTTGCAGTTG[C/T]GTCTACCAGGCAAAA | 388795 |
rs374749769 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907007 | AAGGTCCGCCCCGAC[A/G]GTCCGCCTGACTCCT | 388795 |
rs374784246 | in-del | -/A | 0.00557542 | 0.0525036 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947689 | TTCAAAATTTATGAG[-/A]TGCCACAAAAAACAG | 388795 |
rs374794931 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949892 | GCAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAC | 388795 |
rs374832200 | in-del | -/CTT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895575 | TTTCTTTCTTTCTTT[-/CTT]TTTTTTTTTTTTAAG | 388795 |
rs374838246 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927435 | CTGCAACCTCCGCCT[C/T]CCAAGTACCAGCAAT | 388795 |
rs374882608 | snp | A/C/T | 0.00110319 | 0.0234616 | stop-gained, synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32917349 | CCACTGGCAGACCTA[A/C/T]CACACGGAGGACATC | 388795 |
rs374900576 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909006 | TGGGGGTAAGGGGGC[C/T]CACAAGAAGGTGGAG | 388795 |
rs374908309 | snp | C/T | 9.01917e-05 | 0.00671474 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896546 | AGTTTTTTCTTTCCT[C/T]GGCCTGTTACAATGG | 388795 |
rs374937793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919300 | AACACCACCGTCCCC[A/G]AACACACAATAATTG | 388795 |
rs374970064 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924218 | GTGTGTGCTACTGTG[C/G]CTGGCTCATTAAAAA | 388795 |
rs374971340 | in-del | -/CTGTGGCCTG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890244 | CTCCTCTGGTAGGTG[-/CTGTGGCCTG]GGTCTCTGTGCTCTG | 388795 |
rs374976960 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946554 | CTTGCTGATGTCACC[C/T]ATTTTTTTGTATCTT | 388795 |
rs374980379 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913568 | CATCCCAATAGCCCA[A/C]AAGTCTTAACTTGTT | 388795 |
rs374990809 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886278 | GGCAGGGCAGGGCAC[A/G]CAGCAAGTCCCTGCT | 388795 |
rs374997486 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897029 | CTGCAGAGACGCAGG[C/T]TCCTCTGCTGTTCCC | 388795 |
rs375038815 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936277 | GACCTCAGGCAATCC[A/G]CCTGACTCAGCCTCC | 388795 |
rs375060607 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897408 | ATGACGCACTCAGGG[C/T]GGTCTGGGTGATCCA | 388795 |
rs375077665 | snp | A/G | 0.030665 | 0.119967 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879308 | AGAGTGGCTGGCCCC[A/G]GGAGTAGGTCCCTCT | 388795 |
rs375170282 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928004 | CCCCTCTCCCTCCAA[A/C]CCCTGGAAACCCCCA | 388795 |
rs375200348 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930978 | GCCGGTCACACCCTT[C/T]CTGCCTGCTAATCCA | 388795 |
rs375203905 | snp | A/C | 0.000437904 | 0.0147905 | missense | EFCAB8 | GRCh38.p7 | 20:32909903 | GCTCACCCCTGTGTG[A/C]TGTCCTCTACAGCAA | 388795 |
rs375213060 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875888 | GGGCCGAGGGACTTG[C/T]GAGGAAGGGGATGAT | 388795 |
rs375234149 | snp | A/C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889974 | CCATTGCACTCCAGC[A/C/T]TGGGCGACAGAGAGA | 388795 |
rs375241739 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873903 | TTTTGTTCTGCTGCT[G/T]CTTTTCTTCGTTTTT | 388795 |
rs375242985 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897626 | TTCTTTTTTTGAGAC[G/T]GGGCCTCACTATGTT | 388795 |
rs375245135 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917014 | CACAATGTCCCCCCC[C/G]CTTTAAACCTTAATC | 388795 |
rs375247530 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896034 | CTTTCTGGACAAGGG[G/T]TGCATGTAGTTTGAG | 388795 |
rs375312053 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954178 | TTGCCTGTTTTTTTA[A/G]TGTCATATCCAAGAA | 388795 |
rs375317176 | in-del | -/CACA | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889148 | GCTAGGGAGTTTATC[-/CACA]CAAGGCCCCTATCAC | 388795 |
rs375376102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876177 | GATTCTGGCCCCAGT[C/T]GGGGGACTTGCCTGG | 388795 |
rs375394565 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867918 | TGATCACCACGGCAG[C/G]CTCAACCTCCCATGC | 388795 |
rs375401148 | snp | A/G | 0.000367411 | 0.0135488 | splice-donor-variant | EFCAB8 | GRCh38.p7 | 20:32898624 | CTCTAAGAAACCCAG[A/G]TAAGAAGTGCTTCTC | 388795 |
rs375414815 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875365 | GGTTTGAGGGGCTGG[A/T]GGAGGCAGCCTCCTA | 388795 |
rs375438878 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908249 | GAGACCCATGCTCAG[C/T]GTCTTGCCTTTTTCC | 388795 |
rs375466839 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941029 | GAGGCTGAGGTGGGC[A/G]GATTATGAGGTCAGG | 388795 |
rs375473577 | snp | A/G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912073 | ATAGGGCCAGTCCAT[A/G/T]GGAGTGGCATAGGGC | 388795 |
rs375571922 | snp | A/C | 0.00676609 | 0.0577691 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32911500 | GAGTGGCTGCCTGCG[A/C]GGCACAGTGAGTGTG | 388795 |
rs375622527 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942484 | TTGAGCCTAACAGTT[C/T]GAGACCAGCCTGGGC | 388795 |
rs375661487 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939063 | TCTCTCTTTCTTTCT[C/T]TCTCTCTCCCCAACT | 388795 |
rs375735897 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924366 | ACCATGCCCAGCTAC[A/C]TGTGTTGTTTTTATT | 388795 |
rs375769937 | snp | C/T | 0.000437904 | 0.0147905 | stop-gained | EFCAB8 | GRCh38.p7 | 20:32961289 | GTGCCCAGCAGGGAG[C/T]AGGCTGTGCTGGATA | 388795 |
rs375773810 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931613 | AATACAAAAATTAGC[C/T]GAGTGTGGTGGTGCA | 388795 |
rs375801554 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889508 | TGTGAACATGGATCA[A/G]AGCCCCCTGGGAGGA | 388795 |
rs375839342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935801 | TGAGTGCACCTGGCC[C/T]ACTTTGCTCATTTTC | 388795 |
rs375865552 | snp | A/G | 0.00237473 | 0.0343762 | missense | EFCAB8 | GRCh38.p7 | 20:32959816 | CCCTGATATACCAGC[A/G]GCGAGAGCAGGCGGC | 388795 |
rs375900216 | snp | C/T | 0.000437904 | 0.0147905 | missense | EFCAB8 | GRCh38.p7 | 20:32867669 | GTGCCTGACCTCCAG[C/T]CTGGGTCCCAGCTGT | 388795 |
rs375904277 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883250 | TTTATATCCTTCAGT[C/T]GTAGGGGTAGCTTCA | 388795 |
rs375913537 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891281 | GTTGAAAAAAAAATA[C/T]TGAATTCTGGTTCGA | 388795 |
rs375941211 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952282 | AAAAAGAAAAAAAAA[-/A]TCAGAAGTTTTAAAT | 388795 |
rs375965804 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32961088 | GATCCTGGGTGTCCC[C/T]GGCTCCAACTGGTGC | 388795 |
rs376069973 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956531 | TATCTTTATTTTGCC[A/G]TAAAATTTAAGACTA | 388795 |
rs376108743 | snp | A/G | 0.000184468 | 0.00960208 | missense | EFCAB8 | GRCh38.p7 | 20:32918423 | GACCCTATGTGGAGC[A/G]GGAGAAGTGGACATA | 388795 |
rs376112082 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955419 | GAAGTGTGCACCTGT[A/G]GTCCCAGTGACTCAG | 388795 |
rs376123617 | in-del | -/TCTTT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929436 | TTCTTTCTTTTCTTT[-/TCTTT]CTTTTCTTTTTTCTC | 388795 |
rs376146514 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876512 | GACAATGGGAATATA[A/C]AGCTTTTTAAGCATA | 388795 |
rs376244796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908250 | AGACCCATGCTCAGC[A/G]TCTTGCCTTTTTCCC | 388795 |
rs376246033 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955835 | TTTCTCTATTTTTTG[A/T]TAAAAACGACCCTTT | 388795 |
rs376296572 | snp | C/T | 0.000437904 | 0.0147905 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32961159 | TCAGGTCTACCAAAG[C/T]CTGCACTTCAGTGAT | 388795 |
rs376299412 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932491 | TACAGCGAAGAGTCT[A/G]AGTCCCATTCCTGTT | 388795 |
rs376383714 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872951 | ACAAAAATTAGCCGA[A/G]TGTGATGGTGGGCGC | 388795 |
rs376404590 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905956 | CCCCATAACCCCCAT[G/T]GTTTGCAACCTGTGT | 388795 |
rs376461199 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899314 | GGAGGCTGAGGCAGG[A/G]GAATGGTGTGAACCC | 388795 |
rs376530669 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906999 | CCAAGGACAAGGTCC[A/G]CCCCGACGGTCCGCC | 388795 |
rs376549919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888152 | CACTGCAGCCTCAAC[C/T]TCCTGGGGTCAAGGG | 388795 |
rs376588862 | snp | C/G | | | missense | EFCAB8 | GRCh38.p7 | 20:32889313 | CAGCTTAACCAGACC[C/G]AGCAGCTCTACAACC | 388795 |
rs376600030 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923224 | AGTGCGATGGCTCAC[A/G]CCTGTAATCCTAGCA | 388795 |
rs376611065 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895306 | GGCTTGTTTTATTTT[A/T]TTTAAGATTTTTTTT | 388795 |
rs376698704 | snp | A/G | | | downstream-variant-500B | EFCAB8 | GRCh38.p7 | 20:32962204 | CCCCTCTGGCCCAGA[A/G]GCACCTTTCCAGACC | 388795 |
rs376721254 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913138 | TTCAGTGGGGGAATG[A/T]CTTAGTCCATTCGGG | 388795 |
rs376734583 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871496 | TGCTGTATTCCTTGC[A/T]TTTTTAAAAAATTAA | 388795 |
rs376802724 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885425 | GTCCCTCCTCCTCGG[C/T]GGCTCTCTGTTCTGC | 388795 |
rs376808324 | snp | C/T | | | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32917394 | GTACCGGAACCAGTT[C/T]CTTGGGACCTCCTCC | 388795 |
rs376826799 | snp | A/G | | | splice-acceptor-variant | EFCAB8 | GRCh38.p7 | 20:32909819 | CCTTTCCTCACCTAC[A/G]GATCGGGATCCTAAA | 388795 |
rs376844311 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876737 | TTTGGGAGGCCAAGG[G/T]GGGTGGATCGCTTGA | 388795 |
rs376863681 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882216 | AAAAGAAAAAAAAAA[-/A]CAGCATGCAAATGCA | 388795 |
rs376892913 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878697 | CTTGTGCTTTCTTTC[A/G]AGGCAGCAAAAGTAT | 388795 |
rs376906044 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894833 | AGTAGGAGAGACAGG[C/G]AGGTAAACTGATGAT | 388795 |
rs376929580 | snp | G/T | 0.000882301 | 0.020985 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32878796 | CTACCTTCCCATGAC[G/T]GTCGTCCCCCTGTAA | 388795 |
rs376935070 | snp | C/T | 0.000197103 | 0.00992534 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867755 | GACTGGAGGTAAGGC[C/T]GCTCTGTAGGCTCGG | 388795 |
rs376940341 | snp | C/G | 0.000266205 | 0.0115339 | missense | EFCAB8 | GRCh38.p7 | 20:32917436 | CATCCTCTTCTGGAA[C/G]ACCGGCACACTCAAG | 388795 |
rs376960901 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921984 | ATAAGCATGTGCCAC[A/C]ATGCCCAGCTGCTTT | 388795 |
rs376973003 | in-del | -/TTTA | 0.00239664 | 0.0345337 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860736 | CTGCATCTTGGTTTT[-/TTTA]TTTATTTATTTTTTT | 388795 |
rs376981794 | in-del | -/GGAATT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909585 | CTTGGACTTGGAATT[-/GGAATT]TGGGGTTCTAGGAAC | 388795 |
rs377158656 | snp | A/G | | | missense | EFCAB8 | GRCh38.p7 | 20:32912845 | GTGACAGGATGGAGT[A/G]AGAGAATCACTCATT | 388795 |
rs377234035 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947903 | GACCCCATCTCAATT[-/A]AAAAAAAAAAAAAAA | 388795 |
rs377265709 | in-del | -/TTCT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939063 | TCTCTCTTTCTTTCT[-/TTCT]CTCTCCCCAACTTCT | 388795 |
rs377328304 | snp | A/G | 8.93136e-05 | 0.00668198 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32896482 | AGTTTCCTTGCAGAA[A/G]CTCTTAAATGAGAAG | 388795 |
rs377380166 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889979 | GCACTCCAGCATGGG[C/T]GACAGAGAGAGACTC | 388795 |
rs377381960 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869104 | TGCCCCTGTGTGACT[G/T]AGGGCTTCTGTTTCT | 388795 |
rs377400142 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892746 | TGTCTGGGCAAGGCC[A/G]GAAAGTGTTGTTGGA | 388795 |
rs377413793 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933700 | AAACCTCTTTTTGGC[C/T]GGGCTCAGTGGCTCA | 388795 |
rs377476336 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915000 | GCTCCTAGGCTCAAG[A/T]GATCCTCCCACCCCA | 388795 |
rs377504280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900335 | GGAGTTTTATCTTGG[A/G]CCTCATTATATGTCC | 388795 |
rs377509267 | snp | A/G | 0.000437904 | 0.0147905 | missense | EFCAB8 | GRCh38.p7 | 20:32943792 | GCTTGGAAACTCTCC[A/G]GTGATGCCATTGGTA | 388795 |
rs377517590 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947183 | ATGAAAAATGACCAA[A/T]CTGTTTTGCATTTCT | 388795 |
rs377522738 | in-del | -/T | 0.388775 | 0.207946 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880272 | TCACCCAAGGGTAAC[-/T]TTTTTTTTTTTTTTG | 388795 |
rs377559619 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941259 | CTCCAAACTCTGTTT[A/G]AAAAAAAAAAAAGAA | 388795 |
rs377578398 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861134 | GACGTCCTAGGTGCA[A/G]ATGCACTGATTTGTT | 388795 |
rs377608982 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866191 | GTCAATGTGTGTAGA[C/T]GCTGGGCTAATGAAT | 388795 |
rs377629841 | snp | A/G | 0.000437904 | 0.0147905 | missense | EFCAB8 | GRCh38.p7 | 20:32911585 | CACGTGGAGATGACC[A/G]CCATGGCCCTGGATG | 388795 |
rs377675716 | in-del | -/CAC | 0.00993419 | 0.0697739 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887814 | CTACTGAGTGCTGGG[-/CAC]CACCCTCAATGCTTC | 388795 |
rs377698672 | snp | A/G | 0.0021876 | 0.0330002 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908234 | GCCGGCTACATCCCC[A/G]AGACCCATGCTCAGC | 388795 |
rs377700688 | snp | C/T | 0.000437904 | 0.0147905 | missense | EFCAB8 | GRCh38.p7 | 20:32961572 | TGAAGGCCACCTTCA[C/T]GTCCTCTGTGAAGGG | 388795 |
rs386393644 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888077 | TTTCTTTCTTTTTTT[-/T]TTTTGAGACTGGGTC | 388795 |
rs386813741 | multinucleotide-polymorphism | AA/TC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863544 | CTTCTGCAGGACAAC[AA/TC]CTCTCTATCAGGGGA | 388795 |
rs386813742 | in-del | GT/TAA | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869734 | CTACTGCAGATGACT[GT/TAA]GTATGTTTTCATATG | 388795 |
rs386813744 | multinucleotide-polymorphism | ACA/GCG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881769 | ACGAGTTCCAAACTC[ACA/GCG]AGCCATTTTTACCAT | 388795 |
rs386813745 | multinucleotide-polymorphism | ATG/GTT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885374 | GTTTATGGCGTGCGC[ATG/GTT]TGCGTGCGTGTGCGT | 388795 |
rs386813746 | in-del | CT/TCTCC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921197 | TTCTGATTATTTCTC[CT/TCTCC]TTTTTTTTTCTTGAG | 388795 |
rs386813747 | multinucleotide-polymorphism | AC/GT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921591 | AATAAAAAAGGAAGT[AC/GT]ATGTAAATGAAAAAA | 388795 |
rs386813748 | multinucleotide-polymorphism | CG/GA | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930746 | TGTGAAACAATGCAG[CG/GA]AGGAGTCCTCTCCTG | 388795 |
rs386813749 | in-del | AC/CAA | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950013 | TCAAAAACAAACAAA[AC/CAA]AACAAAACAACAACA | 388795 |
rs386813750 | multinucleotide-polymorphism | AAC/CAA | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950020 | CAAACAAAACAACAA[AAC/CAA]AACAACAACAACAAC | 388795 |
rs397687029 | in-del | -/C | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885140 | TCTGCTCACCCTCTC[-/C]TGGGCAGTTTTTCCT | 388795 |
rs397701420 | in-del | -/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955018 | GGCCACTCTACTCAT[-/G]GGGAGGATAGATGTC | 388795 |
rs397714594 | in-del | -/TT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921712 | TACTTTTTTTTTTTT[-/TT]GACTAGTAATATAAA | 388795 |
rs397743681 | in-del | -/AAT | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899254 | AATAATAATAATAAT[-/AAT]TAGCCGGGCGTGGTG | 388795 |
rs397807396 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921210 | CTCTCCTTTTTTTTT[-/T]CTTGAGACAGGGTCT | 388795 |
rs397864642 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929517 | TTTTTTTTTTTTTTT[-/T]CTTTAAATAGAGATA | 388795 |
rs397864811 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880286 | CTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCAC | 388795 |
rs397865341 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873824 | CAAAAAAAAAAAAAA[-/A]TGCAGTTCACCTCTC | 388795 |
rs397865480 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890019 | AAAAAAAAAAAAAAA[-/A]GCCTCTCCTGCATGC | 388795 |
rs397865894 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878409 | CTGTTGCTTGGCCAC[-/C]TGCCCTGGCCAGTAC | 388795 |
rs398035580 | in-del | -/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932387 | TGTAGTACTGAATAA[-/T]TTTTTTTTTTTGAGA | 388795 |
rs398040727 | in-del | -/C | 0.5 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934288 | ACAGGATTTTTTTTC[-/C]TCTTTTAAGGCTGAA | 388795 |
rs527246901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884966 | GGCCAGGCCTGCCCC[C/T]GGAGCTGTTGGCTGT | 388795 |
rs527251180 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873058 | AGATCGTGCCATTGC[A/T]CTCCAGCCTGGGCAA | 388795 |
rs527264803 | snp | C/G | | | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32918520 | CCTGGTGTCGGCTCC[C/G]CCAGTGATGCGGTGC | 388795 |
rs527286014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890213 | CCCCTCCCTGTGGTG[C/T]TGAGGCCACTGTGGT | 388795 |
rs527295694 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893846 | ACCTCCCATAATCCG[C/T]CCCTACTGTCAGGAG | 388795 |
rs527309205 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895068 | CTCCATCCCTGGGAG[A/G]GAACCTGAGCCTAGA | 388795 |
rs527333038 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927791 | TTGCCCTTTGTCTTT[G/T]GTTCAGGGATTCCTG | 388795 |
rs527363269 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878884 | TGCAGTGAGCCCCTC[C/G]CTCAATCCGTGACCT | 388795 |
rs527378715 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871958 | CTGTCTGGAAGGAGG[A/C]CGCAGGGCTCATGGC | 388795 |
rs527420385 | in-del | -/CAAAAA | 0.0452528 | 0.143452 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872792 | AGCGAGACTCCATCT[-/CAAAAA]CAAAAACAAAAACAA | 388795 |
rs527461854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901217 | GGTGGTATCACTTAG[C/T]GTATATTGGGGTGTC | 388795 |
rs527477694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895362 | CAAGGTCATACTCTG[C/T]TGCCCAGGCTGGAGT | 388795 |
rs527650428 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877605 | ATTTAACCCCCTCGC[A/C]TTCCTAGCATTCTCA | 388795 |
rs527677078 | snp | A/G | 0.000553812 | 0.0166313 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906666 | CAGAAGCTGCTGGGG[A/G]GAGGGCTGCTGGGGA | 388795 |
rs527719746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912685 | CTGTAGGTGATTTTC[A/G]TCATCCAGAGATTTG | 388795 |
rs527720976 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920048 | GGGAAACACCCTCAT[A/C/G]GTGACTTGGGTGCCC | 388795 |
rs527722575 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871307 | GAGATAGGGTTTTCC[C/T]GTGTAGCCCAGGGTG | 388795 |
rs527738968 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907135 | TGGGAGGAAGGTGAG[G/T]GTGGCCATGGACCTC | 388795 |
rs527778245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950047 | AACAACAAAAATGGA[A/G]CATAGAACTAAAGGC | 388795 |
rs527781473 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864287 | ACCTAAGTGTACTTT[C/T]AAAGGGCTGCCTGAG | 388795 |
rs527794368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871027 | CTGGCTAATTTTGGT[A/G]TTTTCAGTAGAGACA | 388795 |
rs527847513 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882760 | GAGTGCAGTGGTGCA[A/G]TCTCGGCTCACTGCA | 388795 |
rs527852320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889148 | GGCTAGGGAGTTTAT[C/T]CAAGGCCCCTATCAC | 388795 |
rs527882227 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904293 | CCACTGTGTCTGGCC[-/T]GAATAGAGTCTTTTT | 388795 |
rs527884206 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941120 | AGCAGGGCATGATGG[C/T]GGGTGCCTGTAATCC | 388795 |
rs527946960 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939495 | TCACTGTATTGGTCA[C/T]GCTGGTCTCAAACTC | 388795 |
rs528064894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909087 | CCAGAAAAGAGATGC[A/G]GGGGCCGCTCGTGCT | 388795 |
rs528071112 | in-del | -/AATTTTCAGATCA | 0.00676609 | 0.0577691 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956457 | AATTCTCAGATTAAT[-/AATTTTCAGATCA]AATTTTCTGATCAAA | 388795 |
rs528072424 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899266 | AATAATTAGCCGGGC[A/G]TGGTGGTAAGCACCT | 388795 |
rs528082655 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936666 | TCTTGTTACATTAGT[C/T]GATGTGTCTATTTTT | 388795 |
rs528107822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905243 | AAGGTTTATGGCTGA[A/G]ACCCTGATAACAAAA | 388795 |
rs528112437 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862880 | TCAGGCAATCCTTCC[A/G]CCTTGGCCTCCCAAA | 388795 |
rs528161366 | snp | C/T | | | missense | EFCAB8 | GRCh38.p7 | 20:32961356 | CTTCCTTGTTATCTG[C/T]CACTGCCTCAGCCTC | 388795 |
rs528172465 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933054 | CCAGGGATGGTGATA[C/G]TATATTATATATGCA | 388795 |
rs528239699 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | EFCAB8 | GRCh38.p7 | 20:32961815 | GCAGAAAATAAATGT[C/T]CTCAGCTGTGGGCAT | 388795 |
rs528284623 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911447 | TGGAGGCCCCGGCCT[C/T]TCCAGCAGCCCCCAG | 388795 |
rs528301386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918003 | AGCTACTGCAGGGGG[A/G]CTCTGGTAGGTGGGG | 388795 |
rs528310665 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888947 | TATTCAAGAGTTTGG[C/T]TGGTTTTTTTTGTGG | 388795 |
rs528345107 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913226 | CAGAGTTCTGGAGAT[A/G]GGGGAAGTTCCAGAC | 388795 |
rs528359003 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956054 | GGTTTCTTTTTTCTT[C/T]CTTTTCTTATTTCTT | 388795 |
rs528369307 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862359 | TCTCAAACTCCTGGA[C/T]GCAAGCGATCCTCCC | 388795 |
rs528376086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946853 | GTCTCTATAGTTTTG[C/T]CTTTTCCAGATTATC | 388795 |
rs528395834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955411 | TGGGCATGGAAGTGT[A/G]CACCTGTAGTCCCAG | 388795 |
rs528451884 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960623 | GGAGCAGGGGATGTT[C/T]GAAAGAGCAGATTTG | 388795 |
rs528462676 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887311 | CCAGGCGCGGAGGCT[C/T]ACGCCTGTAATCCCA | 388795 |
rs528481842 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892997 | TGGTGCCCGCCACCA[C/T]GCTTGGCTAATTTTT | 388795 |
rs528528355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924069 | GTTATTTTTTGTTTT[C/T]TGAGACAGAATCTCA | 388795 |
rs528597919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923633 | ATTTTTTTGTGCATA[C/T]ACAAGTACATACATG | 388795 |
rs528638535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903944 | GGAGCCGGGTCAGGG[A/G]TGACTTCAGTGGAGG | 388795 |
rs528639521 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945213 | ACCCAGGGTTGAGTG[C/G]AGTGGCACGAATTCA | 388795 |
rs528730836 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860966 | GCTGGTCTCAAATTC[C/G]TGGGCTCAAGCGATC | 388795 |
rs528735966 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938227 | ATATGATTATGCCAA[G/T]AGATGCAAAAAGAGC | 388795 |
rs528752871 | in-del | -/T | 0.0240643 | 0.107019 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928600 | TCATTTGTTAGCCCC[-/T]TTTTTTTTGGTGTGG | 388795 |
rs528824254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892709 | CCTGGTCTCCTGGGC[C/T]CGTGTTTGTTGGCTC | 388795 |
rs528827168 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898038 | GTTCAAGTTGCCGTG[A/T]AATGCACATTCTCAT | 388795 |
rs528844852 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860672 | CCATTGTGCCCAGGC[C/T]ATTTTTTCATTCTTT | 388795 |
rs528901320 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941054 | GTCAGGAGTTTGAGA[A/C]CAGCCTGGCCAGCAT | 388795 |
rs528916709 | snp | G/T | | | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32911542 | GACGGGCAGGAAGAC[G/T]ATGGAGTTTGCTGTG | 388795 |
rs528920787 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899991 | CCTGCAGTTTTCCTC[C/T]GGCCCCTAGTCTTTA | 388795 |
rs528920864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894307 | GCTTGTTGGGGCAGC[A/G]TCCCCTGCTGGCAGA | 388795 |
rs528938518 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940524 | GACCTTAGACAGTGT[A/G]TCTTAGATATGACAC | 388795 |
rs528950065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925867 | TGAGACTGAAATGCT[C/T]ACCTTCAGTCCAGCA | 388795 |
rs529027446 | snp | A/G | 0.000277072 | 0.0117669 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32889318 | TAACCAGACCCAGCA[A/G]CTCTACAACCAGCCG | 388795 |
rs529043373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895155 | GTCCCTGACGGTGCT[A/G]GCTCTACTCGTCTGT | 388795 |
rs529073344 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905439 | AACTGTTTGTCCAGA[C/T]CCCCCTCTGTGTCCC | 388795 |
rs529134003 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948919 | AATGGTGAAAGGCTG[A/C]GTACTTTCCCCTGAC | 388795 |
rs529144029 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906328 | GTGGGCTGTTGGTTT[A/G]GGGCCAGGACTGGGC | 388795 |
rs529208079 | snp | A/T | 0.0279526 | 0.114869 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957319 | ATACAAAATAAAATT[A/T]AAAAAAAAAAACCCA | 388795 |
rs529275448 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881887 | ATTCTGACAACGTTT[G/T]AAAACATGGTGACTG | 388795 |
rs529293159 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924137 | CAGCTCATTGTAGCC[A/T]CCACTTCCCAGGCTC | 388795 |
rs529306251 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885427 | CCCTCCTCCTCGGTG[A/G]CTCTCTGTTCTGCCG | 388795 |
rs529353441 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918095 | AAGGTAGCCTCAAAA[A/C]TATTTGGAAACCACT | 388795 |
rs529387146 | snp | A/T | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32876024 | AAGGTGGACTCGGAC[A/T]GTGAAGGCTTTGTCA | 388795 |
rs529424287 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | EFCAB8 | GRCh38.p7 | 20:32961868 | GTGTGTTCCTTGCCC[C/T]CTTAGGTCCTTCCTT | 388795 |
rs529429314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898734 | GTGTATGGACTCTGG[A/G]GTTTAGTTTTTCCAG | 388795 |
rs529435512 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884367 | ATGGCCTGTCCTTAG[A/G]GCTGTCTTCCCTTTT | 388795 |
rs529463246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946792 | ATGTCTCCTCATAGT[A/G]AACTCTATTTCCTTC | 388795 |
rs529470677 | snp | A/G | | | utr-variant-3-prime | EFCAB8 | GRCh38.p7 | 20:32961658 | GGCAACCAGGCCCAT[A/G]GCGGTCCTGCATGTT | 388795 |
rs529541359 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907234 | TCCTTCCCTTTTCTG[A/C]GCCTCAGTCCTCAGT | 388795 |
rs529604269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893570 | GGGTGCAGGACACTT[C/T]TCACCCCAGCATGAT | 388795 |
rs529611235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874677 | CTCCCAAGTAGCTGG[A/G]ATTACAGGCACACGC | 388795 |
rs529637315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887351 | GAGGCTGAGGCAGGC[A/G]GATCACTTGAGGTCA | 388795 |
rs529664893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941187 | AACCTGGGAGGCGGA[A/G]GTTGCAGTGAGCAGA | 388795 |
rs529672533 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953771 | TTCTCCCATTCTGTA[G/T]GCTTCGTTTTCATTG | 388795 |
rs529703522 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869987 | CTTGATTTTTCCCCC[-/T]GAGATAATACTCCTG | 388795 |
rs529758994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867938 | ACCTCCCATGCTCAA[A/G]CGATCCTCCTGTCTC | 388795 |
rs529794062 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879736 | TTCTTGTCCGTGTCC[C/G]TGTGTCTTTGGGCAC | 388795 |
rs529800518 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861032 | ATGAGCCACTGTGCC[A/T]GGCCTGCATCGTGCT | 388795 |
rs529843296 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954481 | TCTTCTATTCCATTG[G/T]TTTATATGTCTGTTT | 388795 |
rs529858873 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902297 | AGGCTGCATAGGATG[G/T]TGGCCTGGAGCTGGG | 388795 |
rs529858902 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931505 | GGCCCACGCCTGTAA[C/T]CCCAGCACTTTGGGA | 388795 |
rs529907746 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886206 | GGGGCTAGTTACAGT[G/T]CTTCTTTACAGTCCT | 388795 |
rs529992899 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921836 | TTACCTTATTCTTTT[C/T]TTTTTTTTTTTTGAG | 388795 |
rs530025084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923160 | CTGCACTCCAGCCTG[A/G]GCAACACAGCTAGAC | 388795 |
rs530060546 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944338 | GGCATGGTGGTGCAT[A/G]CCTGTAATCCCAGCT | 388795 |
rs530068738 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860272 | GAGATTGAGCCACTG[C/T]ATTCCAGCCTGTGAC | 388795 |
rs530101436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897249 | TTGTGTGGTCCGACC[A/G]TTGATTCCTCATGCT | 388795 |
rs530110286 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926508 | TAATCTATCCACTTC[A/G]TTCTTTTTTTTTTTA | 388795 |
rs530122823 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923835 | GCACAGAGTCTGTAT[A/G]GCTATCTGCTGCCGC | 388795 |
rs530198760 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959501 | TAAATAGTCCACAAG[G/T]GGAGGTCCAGATAAA | 388795 |
rs530257549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891467 | AGGTGATCCACCTGC[C/T]TCAGCCTCCCACAGT | 388795 |
rs530282863 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928812 | GGAAAAGCTTTCAGT[A/C]TTTTACTATTGAGTG | 388795 |
rs530321090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943837 | GCTCAGCCATGCCCA[C/T]GGCCCTTCTTGTCTC | 388795 |
rs530360710 | in-del | -/C | 0.0146672 | 0.084371 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903892 | TTGTCCAGGTTGATG[-/C]CCAGGCACCTGGCTT | 388795 |
rs530374655 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902003 | GTTTTTTAAATTAAT[G/T]AATTTTAAATTAATA | 388795 |
rs530389592 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868785 | AGGTCAGGAGTTCAA[A/G]AGCAGCCTGGCCAAC | 388795 |
rs530438187 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931647 | CTTGTAATCCCAGCT[A/G]CTCAGGAGGCTGAGG | 388795 |
rs530450158 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899429 | AAAAAAAAGAAAAAC[C/T]AATTAATCACACAAG | 388795 |
rs530488970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861599 | TAGCCGTTGAAACAC[A/G]TGTTAAAGATTGCCA | 388795 |
rs530519994 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960819 | GATTGCTCCAAGGAG[C/T]TCTTTGCACCTGGGC | 388795 |
rs530535661 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911386 | GTCTGTTTTCTCAGT[G/T]GATGGAGGGGAGGGG | 388795 |
rs530593497 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880971 | CAGCTCCCTTATAGC[A/T]AAAGAATACACAACT | 388795 |
rs530615145 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947379 | ACTTAATTAACATTT[A/C]TAGATCATTCATAAA | 388795 |
rs530629638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887266 | TTCAGTTCAGAGCCT[A/G]TGGTGTCATTCAAAG | 388795 |
rs530638177 | in-del | -/GT | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892711 | TGGTCTCCTGGGCCC[-/GT]GTTTGTTGGCTCCTC | 388795 |
rs530644740 | in-del | -/TG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918640 | CGTTCACACACCGTC[-/TG]TGTGTGTGTTTTCTT | 388795 |
rs530647735 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923612 | CATGTGTTGTAGCCT[C/T]CTAGAATTTTTTTGT | 388795 |
rs530690521 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868050 | GGCTTGCTATTAGGT[C/T]GGTGCAAAAGTAATT | 388795 |
rs530715863 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917228 | CAGAATCCTCAAGGC[G/T]CCAGTGCTTCCCCAA | 388795 |
rs530859295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937639 | CTTTTTTTTTGTTGA[A/G]ACAGAGTCTCACTCT | 388795 |
rs530870454 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934298 | TTTTTCTCTTTTAAG[C/G]CTGAATAGTATTCCA | 388795 |
rs530880001 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901199 | CTATCTGTCTGCATT[A/G]GTGGTGGTATCACTT | 388795 |
rs530915435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892480 | TCTCTCTCAGGGTCA[C/T]CTCTCATGGTCACTC | 388795 |
rs530921134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938120 | TTATACACCATGACC[A/G]AGTAAGATTTATCCC | 388795 |
rs530942706 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926735 | CTCATTGTTCAATTC[C/T]CACCTATGAGTGAGA | 388795 |
rs530944119 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899793 | TGGTCAGGCTGGTCT[C/T]GAACTCCTGATCTCA | 388795 |
rs530951943 | in-del | -/TCCC | 0.121501 | 0.214448 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939019 | CCTTCCCTCCTTCCC[-/TCCC]TCCCTCCCTCCTTCC | 388795 |
rs530974059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960765 | CATGCCCCTGCAGGG[C/T]CCCCCTGTCTCGGGC | 388795 |
rs531043743 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930309 | GGAAACTGGGGGACC[A/C]GGTGGGTGTGGTGAC | 388795 |
rs531092416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945059 | TATCTTCAAGTCTGC[C/T]GATTTTTCCTTCTGC | 388795 |
rs531199388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922201 | TGAAGCTGGTCCTCT[A/G]TGAATAGGTCTGTGG | 388795 |
rs531236278 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860325 | AAGCAAAAAAAAACC[A/C]AGTTATTTTGTAGAA | 388795 |
rs531238703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929414 | AATAAGGATAATTGA[A/G]ATTTTTTTCTTTCTT | 388795 |
rs531259809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915713 | GTCTTGTTTTATGGC[C/T]CAGGCTGGAGTGCAG | 388795 |
rs531389864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890330 | TTTGGCTCTCATCTC[A/G]GAAGTTACTTCCTCC | 388795 |
rs531403696 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950535 | ACAGACTAAGAGTTT[A/T]TAAGGATTCAGGGTG | 388795 |
rs531427230 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886194 | CATCTGTCAAATGGG[A/G]CTAGTTACAGTGCTT | 388795 |
rs531430201 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901938 | TGATTCGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 388795 |
rs531459840 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864322 | GGTATGGTGGCTCAC[A/G]CCTGTAGTCCCAGCA | 388795 |
rs531512062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928003 | TCCCCTCTCCCTCCA[A/G]ACCCTGGAAACCCCC | 388795 |
rs531543564 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947819 | TGGTGCGGTGGCTCA[C/T]GCCTTTGGGAGGCAG | 388795 |
rs531580945 | snp | A/C | 0.000399281 | 0.0141238 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32943653 | TGTGGCTGGCCATAC[A/C]ATTTCCCTGGTTCCC | 388795 |
rs531642488 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907180 | GAGCTGGGTTCCCAG[A/G]TAGCCCAGCCTGGCT | 388795 |
rs531727135 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941507 | ATAAAGTGTGGTATG[G/T]TGATACAATGGAATG | 388795 |
rs531727254 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907839 | CCTCTAGGGAAAGTT[A/C]CTCCACCTGGGAGGA | 388795 |
rs531745126 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895428 | CTCTTGGGCTCAAGT[C/G]ATCCTCCCACCTTAG | 388795 |
rs531792004 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901492 | GTTTTATTGAGTCCT[G/T]ATGGCAGGAGGATAT | 388795 |
rs531821413 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883488 | TCCCATGTAGCATGT[C/T]CAGTTCATATAGCTT | 388795 |
rs531839907 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864847 | AAGAGCTCACTATGA[C/G]ACAAGGAGTAATAAC | 388795 |
rs531861962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950928 | TGGCAGTGTTTGTCC[A/G]AGATGACGGTGCTCC | 388795 |
rs531864349 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871108 | TCCACCTGTCTCGCC[G/T]CCCAAAGTTCTGGGA | 388795 |
rs531907286 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958324 | GGGCTGAGGATAGGG[G/T]CTGCTAGCTGACCCT | 388795 |
rs531922385 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877716 | GTTTTCCAGCAGCTG[C/G]GCAGTGGAATGGAGT | 388795 |
rs531941604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889608 | GATGTTGAACAGACC[C/T]AAATTTACAAGCCAG | 388795 |
rs531945259 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943949 | AAATAATATTACAGT[C/T]TGTCCAATTATCCAT | 388795 |
rs531971162 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909465 | CTTTTTGGAGCACAG[A/T]GGAATCCTTAGCCTC | 388795 |
rs531992018 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899794 | GGTCAGGCTGGTCTC[A/G]AACTCCTGATCTCAG | 388795 |
rs531999876 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916381 | TCCTGCCTCAGCCTC[A/C]TGAATAGCTAGGACT | 388795 |
rs532030436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909964 | CGCCTCTGAGGCTGG[C/T]GGGAACACCAGGTGA | 388795 |
rs532036427 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923059 | GTTTGATAGTGTGCA[C/T]GGTGCACCCAGCTCC | 388795 |
rs532104809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873001 | GGAGGCCGAGGCAGG[A/G]AGAATTGCTTGAACC | 388795 |
rs532140099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891366 | GGGATTACAGGTGCG[C/T]GCTACCACACCCAGC | 388795 |
rs532160951 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915760 | CACTGCAGCCTCCGC[A/G]TCCCGGGTTCAAGTG | 388795 |
rs532166924 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890832 | AAATGGGGCCTATGA[C/T]ACATGACTCCAGGGT | 388795 |
rs532176620 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953411 | CCTCCATACTGTTTT[-/C]CATAGCACATGTACC | 388795 |
rs532176913 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891039 | ACATCTGTTTCCTGG[C/G]GACCCAGTGCTGTCC | 388795 |
rs532239109 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950781 | TAGCAGTTACCCAAG[A/T]GACCTCCCCCTCCCT | 388795 |
rs532256653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866460 | CACATTATGCTAAGT[A/G]TCTGTATCAGTCTCA | 388795 |
rs532299766 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952181 | GAGGCAGGAGGATTG[C/T]TTGAGCCCGGGAGGT | 388795 |
rs532333518 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954324 | GGCATAAAATAACAG[C/T]CCAGTTTTACTCTTT | 388795 |
rs532385483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928626 | TGTGGGAGCTTTAGC[A/G]TTTTCTACATATAAG | 388795 |
rs532393414 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958105 | CCATTGCCATTTTAC[A/C]CACAAGCTACCTGAA | 388795 |
rs532398270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922309 | AGTATATTGAGAGGA[C/T]GGATTCTTGGAAACA | 388795 |
rs532405963 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919208 | ATAATCTCTTGTATG[G/T]GGCAGGAGGAACCAG | 388795 |
rs532407090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865433 | CAGAGCTGGTTAGGA[A/G]GTACTTTGAATGCTA | 388795 |
rs532489506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951784 | CACTTATTAGTTATC[C/T]ATATATCTTCTTTGA | 388795 |
rs532527683 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921778 | AAGTCTATAGCATGG[A/G]TATACTTTCATGAGA | 388795 |
rs532529585 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875789 | GCTGGAATTACAAGC[A/G]TGAGCCACCGCGCCT | 388795 |
rs532658045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959430 | TTGACAGTACAGTGG[A/G]GGGACATCAAACAAG | 388795 |
rs532664506 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864997 | AGGAAACCTGTGGCT[C/T]AGGGAAGTGATGTGA | 388795 |
rs532678069 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896664 | TCTGGAAACAGGTTG[C/T]GGCAGCTGTTGGATC | 388795 |
rs532713434 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878300 | CGGGTGTGGTGGCTC[A/T]TGGTTATAATCCCAG | 388795 |
rs532719924 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923687 | AGATATTTTTCACTG[A/G]ATAATATCATATTGC | 388795 |
rs532741425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914425 | TGGGTTGGCTGATCC[A/G]TACTAATCTCATCAA | 388795 |
rs532768732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920609 | AAACCCATCAGATCT[C/T]GCTGAGACTTGTTCA | 388795 |
rs532804832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907916 | GTTGGTAGCCACTAC[C/T]GGACTGTGTCCCAGG | 388795 |
rs532840002 | in-del | -/TCTT | 0.0182633 | 0.0937982 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939055 | CTTCGTTTCTCTCTT[-/TCTT]TCTTTCTTTCTCTCT | 388795 |
rs532854150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920223 | TGGAGAAGGTTGGCC[A/G]TGATCAGCCAGGGAG | 388795 |
rs532872013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877800 | TTTGAGCATGGGCAT[C/T]TCACATCCTTACAGG | 388795 |
rs532875134 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935054 | ATTGTGGTTTAATTT[G/T]TTTTTCCTAATGATT | 388795 |
rs532904604 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911031 | GCGTGAGCCACTGTG[C/T]CCAGCCTTACCTGCT | 388795 |
rs532941417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907110 | AAGGCCTAGCAGGAG[A/G]GGCCCCGGGTGGGAG | 388795 |
rs532942261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895234 | AATGGTTTCAGCAGC[C/T]GGGAGATGCTAAGCC | 388795 |
rs532958792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900136 | GGGTGAGGCCAGGGT[A/G]GGGTTGGGGCAGAAA | 388795 |
rs532979344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906505 | AGGCTCAGTCTCAGA[C/T]GCTCTCTTGGGGCCA | 388795 |
rs533009792 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927493 | GGGATTAAAGGTGCC[C/T]GCCACCATGCCCAGC | 388795 |
rs533044952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942100 | TTTTTATCTTTGACA[A/G]CCTAAAGAATTTATT | 388795 |
rs533048235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884932 | GCCTGTATGAATGCT[C/T]AAGGGCGGCCTCCTG | 388795 |
rs533086234 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914645 | GGTGGCAGGAGAGAG[A/T]GTGCAAGGGAAACTG | 388795 |
rs533147953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912248 | TCGAGACCAGCCTGG[C/T]TAATATGGTGAAACT | 388795 |
rs533184157 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918858 | AAAGAGAACACAACC[C/G]TGAAAACCTAAAATT | 388795 |
rs533229131 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864941 | TAGGTCTCAACCACA[G/T]CCCTGCAGGGTAGGG | 388795 |
rs533263855 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957417 | TGCTCTTTCCTCTGT[A/G]TAGGGCTGAGCATCT | 388795 |
rs533268616 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864125 | AGGATTACAGGCATG[G/T]GCCACCATGCCCAGC | 388795 |
rs533290838 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888350 | TCTGCCTCAGCCTCC[C/T]GAGTAGCTGGAATTA | 388795 |
rs533303551 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894780 | GTAAGTGCACAGTGA[A/C]TATGCTATGACTTCT | 388795 |
rs533314560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888121 | CAGGCTGGAGTGGAG[C/T]GGTGCAATCACGGCT | 388795 |
rs533351222 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893719 | CTGCCTTTGGGTGGG[C/G]AGGGGCTGTCCTGGA | 388795 |
rs533362040 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937232 | TGATCCGACTGCCTC[A/G]GCCTCCCAAAGTGCT | 388795 |
rs533471703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888393 | ACCACGCCCAGCTAA[C/T]TTTTGTATTTTTAGT | 388795 |
rs533509694 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870910 | GTCACCCAGGCTAGA[A/G]TGCAGTGGTGCGATC | 388795 |
rs533638109 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950515 | GGTTAGAGCCACACT[C/T]TCTTACAGACTAAGA | 388795 |
rs533767053 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888950 | TCAAGAGTTTGGTTG[G/T]TTTTTTTTGTGGGGG | 388795 |
rs533788280 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877275 | GTGCAATGGCACGAT[A/C]TTGGCTCTTTGCAAC | 388795 |
rs533841643 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907476 | TCCCACTTGGGACCC[A/G]CCACTGTGCTCCTCT | 388795 |
rs533856751 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926097 | CCAGTCCTGCTGAAG[G/T]CCTGGGCGCTCATTC | 388795 |
rs533864313 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864514 | TTGAGCCTGGGATGT[C/G/T]GAGGCTACAGTCAGC | 388795 |
rs533894890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913707 | CTGTGAACCTGTGAT[A/G]CTAACACGTTATGTA | 388795 |
rs533914139 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937625 | ATTTAAAGATTTTTC[-/T]TTTTTTTTGTTGAGA | 388795 |
rs533914195 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909695 | CTGGAGTCTTGCTGG[A/C]ATCAGGCCTGCGTGT | 388795 |
rs533927864 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899569 | AAGCCACCACTTCTG[G/T]TTTTTTTTCTTTTTT | 388795 |
rs533929761 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871281 | ATTTTTATTCTTTTA[A/C]ATTTCTTTTAGAGAT | 388795 |
rs533983731 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942116 | CCTAAAGAATTTATT[A/C]GTGGTATTCATCTGA | 388795 |
rs533993497 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894434 | CTGCTTGAGCCTAGT[A/C]ACTCTGCGCCACCGT | 388795 |
rs534012789 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894900 | TGCCTGTGCACAACC[A/T]GCCCCACTCTGGCAG | 388795 |
rs534021277 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933353 | TGTTTCAAATAGATA[A/C]ATCATAATTGTAGAC | 388795 |
rs534049179 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940057 | TTCCTTCCTTCCTTC[C/G]TTCCTTCCTTCCTTC | 388795 |
rs534064124 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927796 | CTTTGTCTTTGGTTC[A/G]GGGATTCCTGTTTTT | 388795 |
rs534079908 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866917 | CTCTTTCTTTCTTTC[A/G]TTTCTTTCGTTTCTT | 388795 |
rs534196762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904965 | GTAGAAGGAGCTGGC[A/G]GGGCAGGATGTTGTG | 388795 |
rs534226920 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868823 | AACCCCGTCTCTACT[A/G]AAAATACAAAAATTA | 388795 |
rs534269637 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869195 | CTGTTTGCAAGGCTC[A/T]AGCCAACAACAGGGA | 388795 |
rs534295216 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953642 | TTGGAGAAATAAATA[A/T]CTATTCAAGTCTTTT | 388795 |
rs534301365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887550 | ACTGTGCTCTAGCCT[A/G]GGCGACAGAGCGAGA | 388795 |
rs534319035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949505 | TTTCAAGACTTATTG[C/T]GAAGCCATGGTAATC | 388795 |
rs534368453 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | EFCAB8 | GRCh38.p7 | 20:32962158 | CCTCCTGGCTCTGCC[A/G]CTGTCAGGCTATGGA | 388795 |
rs534386658 | in-del | -/AAT | 0.1679 | 0.236135 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899232 | TACTAAAAATACAAT[-/AAT]AATAATAATAATAAT | 388795 |
rs534411664 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889923 | AGGAGAATCGCTTGA[A/G]CCTGGAGGTGGAGGT | 388795 |
rs534478370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954668 | TAATTTAGCTCTATG[A/G]TCCATCTTCAATTAA | 388795 |
rs534510525 | snp | C/T | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32961334 | CCTGCGGCCGCCTCC[C/T]CCCCATCTTCCTTGT | 388795 |
rs534513568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953936 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGCTTAC | 388795 |
rs534529750 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862498 | CTTGCTTCTTGGCTT[C/G]CAAATCTCCTTCCCT | 388795 |
rs534554101 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876199 | CTTGCCTGGTGGAGA[A/C]GTCCCTCCTAAGACC | 388795 |
rs534557652 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909144 | CCGTGGGCTGGGCCA[A/C]CCTGGTCGGTGACAT | 388795 |
rs534572629 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898223 | TGATTAGTATGGGCC[C/T]GACCTTCCCCATCCT | 388795 |
rs534590703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893744 | CCTGGATGTGGGCTC[C/T]GTGGAGCCTGGGCAT | 388795 |
rs534603790 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938620 | ATATACAAAACCAAT[A/T]TATTTATATACACTA | 388795 |
rs534615250 | in-del | -/CTTC | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939598 | GGCTGGCTTTCTTTT[-/CTTC]CTTCCTTCCCTCCTT | 388795 |
rs534616171 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905949 | TCCTAAACCCCATAA[A/C]CCCCATTGTTTGCAA | 388795 |
rs534723049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932242 | ATCAGCTGGGTGTGG[C/T]GGTGCACGCCTGTAA | 388795 |
rs534729294 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923852 | CTATCTGCTGCCGCT[G/T]GGTTTTGCCTCTATA | 388795 |
rs534788317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868182 | TCCTGCCTTGGCCCC[C/T]GGAGTAGCTGAAACT | 388795 |
rs534812170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897877 | GAAATATTTGATGAG[C/T]CAATCTCTCCAACCC | 388795 |
rs534819423 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917005 | CTGTAAGGCCACAAT[G/T]TCCCCCCCCCTTTAA | 388795 |
rs534828926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32961070 | TCCTGTGAGTCTACT[C/T]TTGATCCTGGGTGTC | 388795 |
rs534842253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936791 | ATTGTTTTGGCTAGC[C/T]AGGGTCTTTTATGAT | 388795 |
rs534849935 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910771 | TTTTTGCCAGGGTCT[C/T]GCTCTGTCGCCCAGG | 388795 |
rs534886714 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891715 | GGTGGCCGGCCACGT[A/C]GAGAGGCAGAGGAGG | 388795 |
rs535000547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929787 | CTATGCTCTCAGCCT[C/T]CTGCTGGGTGCCAGG | 388795 |
rs535021018 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886828 | GGAGTAGGCCTCCCA[G/T]GACCACACACCCACT | 388795 |
rs535037792 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879855 | GACTCAGTATGCTGC[A/G]GTGCCCTATTTGGGG | 388795 |
rs535064562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916053 | TGGTACCAGTTTCTG[C/T]CTTTGTTCACTCAGG | 388795 |
rs535091356 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882343 | CAGCATTTCCTCGTT[C/G]GTCACTTGATAGCTG | 388795 |
rs535093205 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910211 | TTGGGTCAGCTCTGG[A/T]CTGGGCCTTCTTGAT | 388795 |
rs535121685 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861407 | AGTTCTCCTGCCTCA[A/G]CCTCCTGAGTAGCTG | 388795 |
rs535146096 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936437 | TCTTCTAGTTGTTTT[A/G]CAGTCTCAGATCTTA | 388795 |
rs535155314 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878603 | GCTCACTGCAAGCTC[C/T]GCTTCCCGGGTTCAC | 388795 |
rs535229955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946954 | ATCTTTGTTGTTGAA[C/T]GTATCAGTAGTTTGT | 388795 |
rs535290588 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951828 | AGATCTTTTGCCATT[-/A]AAAAAAAACTGTGTT | 388795 |
rs535312745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922581 | GAGGACAATGGAGGA[C/T]AAGAAAGCCGGGAAG | 388795 |
rs535369513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932361 | CAGCCTGGGCGACAG[C/T]GTGTGACTCTGTCTC | 388795 |
rs535415155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888686 | AATGGAAGCATATTA[C/T]AATGTTGCTTTTTAC | 388795 |
rs535426624 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866078 | TGGGTGTGTAGTGAG[A/T]GCCTTCACGTGCTCC | 388795 |
rs535455043 | snp | C/G | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32961463 | ACAGCCCATTCCACC[C/G]CCTCGGTCCCATCCC | 388795 |
rs535478392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933162 | GACTCGTCTAAGCTC[C/T]AGTAGCAACCAGTGT | 388795 |
rs535485265 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924535 | TTCCCATTTTATGGC[C/T]GAAGAAACAGGCCCA | 388795 |
rs535548556 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904375 | GCATGATCACAGCTC[A/G]CTGCAGCCTCAACCT | 388795 |
rs535554257 | in-del | -/T | 0.194278 | 0.243711 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928240 | GCAACTGATTTTTTA[-/T]TTTTTTTTTTTTTGA | 388795 |
rs535584213 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882901 | GGGGTTTCACCATGT[C/T]AGCCAGGATAGTCTC | 388795 |
rs535585810 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954772 | GAATTCTGTCAAACG[C/G]TTTTTCTGCTTCTAC | 388795 |
rs535586685 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910830 | GCAGTCTCTGCCTTC[C/T]GGGTTCAAGCGATTC | 388795 |
rs535637937 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873244 | GACAGACCCTAGGAA[-/G]GGCTTCCCTATGGAA | 388795 |
rs535642074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893432 | GCGTCTGCTTCCAAG[C/T]GCAGGGTGCATGCCG | 388795 |
rs535643742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898941 | AAGGGTGTGAAAGCA[C/T]GTACCTCACTTCCTG | 388795 |
rs535673500 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904862 | GAACTCCTGACCTCA[G/T]GTGATCCGGCCGCCT | 388795 |
rs535682471 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898373 | TGATCACTAGGAGAA[A/G]GGCATTAGACTCCGT | 388795 |
rs535694343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892782 | CCTTGCTTCCAAGGA[A/G]GAGGGAAGCTGTTGG | 388795 |
rs535729631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923710 | CATATTGCATGTATT[A/G]TTCCGGGACTTGCTG | 388795 |
rs535729992 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917016 | CAATGTCCCCCCCCC[C/T]TTAAACCTTAATCCT | 388795 |
rs535837028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898199 | CATCCTTTCTCTCCT[C/T]GTGGGAGATGATTAG | 388795 |
rs535839298 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927431 | TTCACTGCAACCTCC[A/G]CCTCCCAAGTACCAG | 388795 |
rs535853428 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925263 | CTCACTCTGTTGTCC[A/T]GGCTGGAGTGCAGTG | 388795 |
rs535854469 | snp | A/C | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32961156 | GCCTCAGGTCTACCA[A/C]AGCCTGCACTTCAGT | 388795 |
rs535867139 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874272 | CCATCACCTAGGCTA[C/T]AGTACAGTGGCAAGA | 388795 |
rs535880993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902922 | GTGTGGACTGACCCC[C/T]GGCGTCTCCCCGACT | 388795 |
rs535915137 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942987 | AATTTAAAGTTTATT[A/T]TTCTGACTTTCCATA | 388795 |
rs535938324 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948506 | AAATCTGACAAAGAC[A/G]TTATAAGAAGAAAGT | 388795 |
rs535948098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937751 | AGCCTCCCGAGTAGC[C/T]GGGATTACAGGCATG | 388795 |
rs535985863 | snp | A/T | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859719 | AAACCATTTGAGAAT[A/T]ACAGACATCATGCCC | 388795 |
rs536068633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886394 | CCAGGGCCGTCCAGA[A/G]TCCTCCAGCAGACGA | 388795 |
rs536116289 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958208 | TTAGGCCTGAGCTCC[G/T]AGTGTGTCCTAGGGC | 388795 |
rs536126891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909525 | TTCCCGGAGGGAACA[C/T]CTGATTGAGGCTTCA | 388795 |
rs536135112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866645 | TGGGGCAGGTGAGCT[C/T]ATCTGACCGAGATGG | 388795 |
rs536183778 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897436 | CCAACAGGCCTGCAC[G/T]GACTTTTTTTTTTTT | 388795 |
rs536213520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944573 | AAGCTTTGTATTTTC[A/G]TATGCTTTCATGTTC | 388795 |
rs536229040 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885355 | TTGGAAGAGCCAGCT[A/C]TGGGTTTATGGCGTG | 388795 |
rs536269741 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957503 | CAGTTTGCCTCTGTG[C/T]TCAGTTGTCTCAAGG | 388795 |
rs536376995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878685 | TACCCTGCCTCCCTT[A/G]TGCTTTCTTTCGAGG | 388795 |
rs536402692 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872738 | GGTGGAGGTTGTAGT[A/G]AGCCAAGATCATGCC | 388795 |
rs536402784 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880726 | TGTGTAGGGCGAGGT[A/C]TGGGGAGAGGGATGC | 388795 |
rs536420966 | snp | C/T | 0.000477593 | 0.0154457 | stop-gained | EFCAB8 | GRCh38.p7 | 20:32959818 | CTGATATACCAGCGG[C/T]GAGAGCAGGCGGCGC | 388795 |
rs536452196 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959052 | CACTGCATCTTTATT[C/G]CTGACCAAGTCTCCA | 388795 |
rs536463563 | snp | A/G/T | 9.95173e-05 | 0.00705328 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867756 | ACTGGAGGTAAGGCC[A/G/T]CTCTGTAGGCTCGGT | 388795 |
rs536483106 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908167 | TTAGAAGTGCTTGGA[C/T]GGACGATGTGCCCTG | 388795 |
rs536530818 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860062 | GTAATCCCAGCACTT[C/T]GGGAAGCCAAGGCGG | 388795 |
rs536552701 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861205 | CTATGAATGATGCTG[C/T]AGCAATCACTCTTCA | 388795 |
rs536554980 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908970 | AGATTGGGACAAGCA[C/T]GAGGGGCTTCCTGTG | 388795 |
rs536562972 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894585 | GGACAAACATGACGA[C/T]GAGGTGGGCCCAGTG | 388795 |
rs536583676 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952223 | TAATCTGTGATTGAG[C/G]CACTGCACTACAGCC | 388795 |
rs536590183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866025 | TAGGAAGAAGAGGGA[A/G]GAGCTGAAGGCGGTG | 388795 |
rs536605883 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928237 | AAATGCAACTGATTT[A/T]TTATTTTTTTTTTTT | 388795 |
rs536667568 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872330 | CATAAGGCACAGAGA[A/G]CAATGCCTGGCATGA | 388795 |
rs536679382 | in-del | -/TCTC | 0.00398564 | 0.0444627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939261 | TCCTTCCTTCCATAT[-/TCTC]TCTCTCTCTCTCCTT | 388795 |
rs536711290 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928118 | TCACTTAGCATAATG[C/T]CCTCTTTGATTAATT | 388795 |
rs536734265 | snp | C/T | 0.00109606 | 0.0233844 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931362 | TACTGGAGAGTTGCT[C/T]AGGAAAGTGCCTTTG | 388795 |
rs536783447 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894252 | TTACTAAGCAGGACA[C/T]TCCAGGGGTTCCCAG | 388795 |
rs536801234 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874022 | GCCTCTCAGGCTCAA[C/G]CAATCCTCCCAGCTC | 388795 |
rs536816271 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32961012 | AGCCACAGTCCTCTG[A/G]ACACACGCCTTCTTG | 388795 |
rs536828000 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937816 | TAGAGACAGGGTTTC[A/T]CCACATTGGCTAGGC | 388795 |
rs536833740 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901573 | TGCCTTCCTGACCTC[A/G]TTGCCTCCACCTGCC | 388795 |
rs536862461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873320 | TCTTGACCTCGTGAT[C/T]CACCTGCCTCGGCCT | 388795 |
rs536896607 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904801 | CTGGCTAATTTTTGT[A/G]TTTTTAGTAGAGGCG | 388795 |
rs536906402 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930172 | GTTACTAAGGACAAA[A/G]TAGTGAACAAAAAAG | 388795 |
rs537007335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946263 | GTCTGCATGTTGGAT[A/G]TACATCTCAGTCTTT | 388795 |
rs537049730 | in-del | -/ACACAGAG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902383 | TATTTACACACACAA[-/ACACAGAG]ACACATGTTCCCTTC | 388795 |
rs537061851 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929638 | TGAGCCACCATGAGA[-/T]TTTTGATAATCGAGA | 388795 |
rs537125868 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923410 | AGAATTGATTGAACC[C/T]GGGAGGCGGAGGTTG | 388795 |
rs537196616 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872795 | CGAGACTCCATCTCA[A/T]AAACAAAAACAAAAG | 388795 |
rs537208666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943985 | AAACGGTCCATCCAT[C/T]CACCCATCCACCCAA | 388795 |
rs537211185 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859931 | GATTCAATTCAGAAT[C/T]GTGCATTGCCTTTAG | 388795 |
rs537222473 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953055 | TTTAGTTACTCACCT[A/C]AGTAGAATAATACAA | 388795 |
rs537239145 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903031 | CCTCTTAGCAGCCTC[A/G]CCGTGTCCCCTCAGG | 388795 |
rs537262429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902164 | ACTAGATATAAGCAC[A/G]GTTCTGGGATGGTTT | 388795 |
rs537272774 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916599 | ATTCCATTTATGAGG[G/T]TTTTGCCCTTCTGTC | 388795 |
rs537303491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897364 | CTTGGTGGGCTCCCA[A/G]TACATTTGCTGCACA | 388795 |
rs537370536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936104 | GTGGTGCAATCTCAG[C/T]TCACTGCAACCTCTG | 388795 |
rs537379169 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944684 | TCTTGTTTTTATTTA[A/T]CTGGGAAAATTTTTA | 388795 |
rs537453091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958641 | GCCTCTACCTGGGTT[A/G]GGTAGAGCTAGGCAT | 388795 |
rs537457163 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878578 | TGCGGACTGCAGTGG[C/T]GCAATCTCGGCTCAC | 388795 |
rs537495409 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917929 | ATCAAAGCAGGAAGG[A/G]ACCTTAGGGGCCGCC | 388795 |
rs537543737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915439 | TTTCCTCTAGTTTCC[A/G]ATAACATGTTTCTCA | 388795 |
rs537617042 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890687 | ATGGGAGGAGAGAGA[A/G]TGGCTGTTCTGGAAC | 388795 |
rs537618830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896758 | AGCCCTGGTCCTGGC[C/T]GACACCGCCTCGCTC | 388795 |
rs537669213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883792 | GTCTCCCGGGTTCAA[A/G]CGATTCTCCTGCCTC | 388795 |
rs537833807 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942979 | TTGTTTAAAATTTAA[A/T]GTTTATTATTCTGAC | 388795 |
rs537846617 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895023 | TGTTTGGCATGAGCC[A/G]CCAGATCCATCCTTG | 388795 |
rs537858813 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912957 | CTTTCCTGGTGGTTG[A/G]AACACCATGCAGGAA | 388795 |
rs537883287 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900515 | ACAGGCACGTGCCCC[C/T]GTGCTCAGCTAATTT | 388795 |
rs537898849 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901857 | CATGCCCGGCTAATA[C/T]TTGCATTTTTAGTAG | 388795 |
rs537901371 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907040 | TGTTCCTCAGGGAAA[C/T]ACACTGGCCAGAGAA | 388795 |
rs537914375 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889496 | TGGCTGAGCAACTGT[C/G]AACATGGATCAGAGC | 388795 |
rs537921680 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859368 | TTCTAAATATCAACC[C/G]AGTTTTACATCTCAG | 388795 |
rs537930818 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926218 | GAACTTTGTGGTGCA[G/T]CACTTTGGTGAATCC | 388795 |
rs537982941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865221 | TCATCTGAAAGTTAT[A/G]GAAGAGCTCCTTGGG | 388795 |
rs538002526 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869657 | ACCACACTCCAGGGG[A/T]GGGGATCGAAGGAGG | 388795 |
rs538028570 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896385 | CAACTCAAGACGTCT[C/T]CTGAGGCTTTGCTTG | 388795 |
rs538030115 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957125 | TTGATTCTTTTCTAT[A/T]GATTGCAATTCTTTT | 388795 |
rs538031624 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884608 | GGGTTATCCTTAAGC[C/T]CAGGGTCAGACCAGG | 388795 |
rs538046789 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905907 | TGTTGTCTCAAATGC[C/G]AAGATGCCATATTTT | 388795 |
rs538069112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889880 | GGTGGCACACGCCTG[C/T]AATCCCAGCTACTCA | 388795 |
rs538085177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912388 | AGTGAGCCGAGATCC[C/T]GCCATCGCACTCCAG | 388795 |
rs538085561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927086 | GGAGCCTAAAACTTT[C/T]GCAAGAAAAATGCAC | 388795 |
rs538168292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877945 | GCTGTGCTCTTTCAG[C/T]GAATGCTGCGAGTAG | 388795 |
rs538187481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870683 | TTTAAAAACTTTTTG[A/G]TAGAGATGGGGTCTT | 388795 |
rs538194993 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863231 | AGACCCTAACAAAAC[A/G/T]CTGTCATCCATCTCA | 388795 |
rs538201324 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941497 | TTCCAAATGGATAAA[A/G]TGTGGTATGGTGATA | 388795 |
rs538238700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902240 | TGTCCATGGGCAGGG[A/G]TGGTGGTGAACACAC | 388795 |
rs538257333 | in-del | -/A | 0.25214 | 0.249991 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899404 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 388795 |
rs538275465 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908840 | GGCCACGTCCGAGCA[G/T]CATCTCTGCAGGAGA | 388795 |
rs538309287 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937882 | ATGGCCTCCCAAAGT[G/T]CTGGGATTACAGGCG | 388795 |
rs538337001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936190 | GGCGTGTGCCACCAT[A/G]CCTAGCTAATTTTTG | 388795 |
rs538343532 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944507 | GACTTATGTGCCACT[A/G]TTACAGTATTACAGC | 388795 |
rs538461705 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923292 | GGAGTTCGAAACCAG[A/C]CTGGGCAACACGGTG | 388795 |
rs538502506 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906749 | TGGCTTCCTCTCCTG[A/C]TGCTCTTGTCCCCAC | 388795 |
rs538510819 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863643 | ATCCACTGCTCGCTG[C/G]GAGTGTCCATGGGCA | 388795 |
rs538521823 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915194 | GGCATGTACCACTGC[G/T]CCTGGATTCTGCTTC | 388795 |
rs538533331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949587 | ACAGAAAGTCCAGAG[A/G]TATATCCATACATAT | 388795 |
rs538542347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872570 | GCGAGCTGAGGTGGG[C/T]GGATCAAGAGGTCAA | 388795 |
rs538575396 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948482 | AACTCATGAGGCAAC[A/T]TGGTACCAAAATCTG | 388795 |
rs538592257 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952128 | AAATTAGCCAGTTGT[G/T]GTGGTGCATGTCTAT | 388795 |
rs538603166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879160 | TGTGCTAGTTGGTGC[A/G]GAGTGGGTCTGGCAG | 388795 |
rs538606881 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923060 | TTTGATAGTGTGCAC[A/G]GTGCACCCAGCTCCT | 388795 |
rs538607252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943137 | ATTGCTCACCCTATT[C/T]ATCTCCCAATACCCA | 388795 |
rs538644842 | snp | A/G | 0.000798403 | 0.0199641 | missense | EFCAB8 | GRCh38.p7 | 20:32959800 | CGGGATCTGGCTGAG[A/G]CCCTGATATACCAGC | 388795 |
rs538658713 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919014 | ACACAGACAAACCAC[C/T]TTCCTCCTCCTCTGA | 388795 |
rs538736065 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860405 | TGTATTTTTTTGGCA[A/G]TAATACTACTGAAGC | 388795 |
rs538753029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944085 | ATAAACTTAATTGTT[A/G]CATTGTATATAAAGA | 388795 |
rs538780631 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927276 | CTTCATGAACTTCAC[C/G]AGTAAATCTGCCACT | 388795 |
rs538789225 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890516 | GGGACTGCATCTGTT[C/G]TGCTCAACTCAGTGT | 388795 |
rs538819930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949720 | CAATTCAAAATGGGC[C/T]ATGCATGATGGTTCA | 388795 |
rs538822405 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863711 | TCCACCTTTCTGTGA[A/C]CTGGCTAAGTCAGCC | 388795 |
rs538822552 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871147 | GTGAGCCACCGTGCC[C/T]GGCCCTCTCTACTTC | 388795 |
rs538824823 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900262 | CTCCTCATTTTACAG[A/T]TGGGAAACCCGAAGC | 388795 |
rs538849154 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900554 | TTATTTTTCATTTTT[A/T]AATTTTTATTATTTT | 388795 |
rs538858480 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960849 | CCTCACCCAGGGTCC[A/T]GCTCGAGGCCTCATT | 388795 |
rs538917517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865323 | GTATGGGAGACACAC[A/G]TGAGTAAGCACCGAA | 388795 |
rs538956423 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864452 | TTAGGCATGGTGGCA[C/T]ATGCCTGTGGTCCCC | 388795 |
rs538969183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872167 | TGGGTGTTGTATAAG[A/G]AGAATAGAATGGGGT | 388795 |
rs538978270 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959232 | CTGCAATTTTATGTG[A/T]TAAGTAATGAGAGTA | 388795 |
rs538981008 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871819 | TGTAAGTTCCCTTTT[C/G]CTAGCTTCAGTCCAG | 388795 |
rs539022847 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876377 | TGGTACCACGACCAT[C/T]TCATGACCCTTCACT | 388795 |
rs539087359 | snp | A/C | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860902 | TGTCACCATACCCAG[A/C]TAATTTTTTGTATGT | 388795 |
rs539087539 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915831 | TGTGTGCCACCACAC[C/T]TGGCTAATTTTTTGT | 388795 |
rs539223581 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907380 | CCCTGCCCTCGATCT[A/G]CACCTCTCAGTTGCT | 388795 |
rs539259330 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933744 | AGTACTTTGGGAGGC[C/T]GAGGCGGGCAGATCA | 388795 |
rs539263012 | snp | C/T | 0.000203066 | 0.0100743 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32906856 | AGTGACTGGTGGCTA[C/T]GATGCCTTCATCCGC | 388795 |
rs539274814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900954 | TGATCCGCCCACCTC[A/G]GCCTCCCAAAGTGCT | 388795 |
rs539321665 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937459 | AAAACCTCAGAAAGA[C/T]ACAAACTACTAAAGC | 388795 |
rs539328510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925280 | GCTGGAGTGCAGTGG[C/T]GTGATCTCAGCTCAC | 388795 |
rs539333539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933795 | ACCAGCCTGGCCCAC[A/G]TGGTGAAACCTTGTC | 388795 |
rs539372709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933243 | ACCATCTGCTCTTAG[C/T]TTTATAATGATATAT | 388795 |
rs539375338 | snp | C/T | 0.000798403 | 0.0199641 | missense | EFCAB8 | GRCh38.p7 | 20:32961323 | CGGACAGCACGCCTG[C/T]GGCCGCCTCCTCCCC | 388795 |
rs539417026 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955600 | TGCCCTCTCAGTATT[C/T]GAGAGTCCTGTTTGG | 388795 |
rs539425804 | in-del | -/CTGT | | | downstream-variant-500B | EFCAB8 | GRCh38.p7 | 20:32962047 | TGTCTTCTGCCCCTG[-/CTGT]CTGTCAGTCTTCCCT | 388795 |
rs539437862 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904873 | CTCAGGTGATCCGGC[C/T]GCCTTGGTCTCCCAA | 388795 |
rs539463322 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866390 | TCATCTAATTATCCA[A/C]GTTAGAGTCTTTTAG | 388795 |
rs539485306 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959144 | TAGGTTCTAGAAATA[A/C]AAGACATCCAGACAC | 388795 |
rs539504920 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899000 | TATGTGTTCAGTAAC[A/T]GGCAGCATTGGTTCT | 388795 |
rs539520325 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919790 | AGGTGTGAACCACCA[C/T]GACCGACCTTTATCC | 388795 |
rs539584671 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874233 | CCTTTATTTTATTTA[-/T]TTTTTTAGAGACAAG | 388795 |
rs539632049 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912153 | TCAGAAAGTGTACTT[A/G]GCTGGCCAGGCAGTG | 388795 |
rs539632943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899466 | TTAAATGCATTGTCC[A/G]TGTAAAAAATGAAAA | 388795 |
rs539635167 | in-del | -/GA | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922779 | CAAGGGCCCACATGG[-/GA]GAGAGCTGGCATGGA | 388795 |
rs539661884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893859 | CGCCCCTACTGTCAG[A/G]AGGGAGGAGCCGCTG | 388795 |
rs539684559 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923763 | GCATCTCTTCATGAC[A/G]GTGTTTACGGAGCCA | 388795 |
rs539707792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911060 | CTACTCTTGCATTAT[A/G]ACAATGGTCATGGTG | 388795 |
rs539709771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918234 | GATGCCTTTAAGGGG[A/G]CTAGGTTTCTGGGAA | 388795 |
rs539746872 | snp | C/T | 0.000620705 | 0.0176059 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32917439 | CCTCTTCTGGAACAC[C/T]GGCACACTCAAGCCC | 388795 |
rs539794124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875143 | TTTTTAGTGCCTCCC[C/T]TCCCCACACTGCTGT | 388795 |
rs539812860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948765 | TAAAGTGAAAAACTA[C/T]GTGATTATCTTGATA | 388795 |
rs539816418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869158 | CCTACAGTTCCTGGC[C/T]ACGCAGGATTCACCA | 388795 |
rs539846696 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919102 | GGGGAGTAGGGAGAA[A/G]GAGCAGGAGGAGTTA | 388795 |
rs539850077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957260 | TTCTAATGCCTATTT[C/T]TTCTCTTGATTATTG | 388795 |
rs539878099 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905637 | TGGTGGTGTGTACCT[C/G]TAATCCCAGCTACTC | 388795 |
rs539915396 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951090 | TGAAACTCTCCTGCA[C/T]GGCTAATGGGAATAT | 388795 |
rs539917700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863125 | GCGTGTCTTGGGCTT[A/G]ACTATTTCTTGGCTG | 388795 |
rs539950978 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862567 | GTTGCCAAGACACTG[C/G]TAGATTAGAGCATTC | 388795 |
rs539972117 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949898 | CCAGCTACTCGGGAG[C/G]CTGAGGCACAAGAAT | 388795 |
rs539996800 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925350 | TCAACCTCCTGAGTA[A/G]CTGGGATTACAGGTG | 388795 |
rs540025562 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909517 | GGGAGGGCTTCCCGG[A/G]GGGAACACCTGATTG | 388795 |
rs540046412 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892743 | AGGTGTCTGGGCAAG[A/G]CCGGAAAGTGTTGTT | 388795 |
rs540088587 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935302 | GCCTCCCGGGTTCAA[A/G]CAATTCTCCCGCCTC | 388795 |
rs540124005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868403 | TCTCCTGTAAAACTT[C/T]CAAGCATTATGTAGG | 388795 |
rs540185796 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869425 | ATTTTTAGTAGAGAC[A/G]GGGTTTCTCCATGTT | 388795 |
rs540217836 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939030 | TCCCTCCCTCCCTCC[C/T]TCCTTCCTTCCTTCG | 388795 |
rs540238934 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907512 | TGTAGGCTCAGGATA[C/T]TGCCCCGTCTGCTGG | 388795 |
rs540273566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939116 | CTTCCTTTCTTTCTC[C/T]CTTTCTTTCTCTTTC | 388795 |
rs540276662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936674 | CATTAGTCGATGTGT[C/T]TATTTTTATGCCAGC | 388795 |
rs540300015 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933705 | TCTTTTTGGCCGGGC[C/T]CAGTGGCTCAAGCCT | 388795 |
rs540300776 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893542 | GATGGGAGGCTGTGC[A/G]GGTGCGGTCTGGGGG | 388795 |
rs540317979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941834 | ATTGAATGAGCACTT[C/T]AAATTGGTAAATTTT | 388795 |
rs540324743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924695 | TTGGGCTTTTTACGT[A/G]GCCTGGTGATCTGTG | 388795 |
rs540342118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899946 | TAGGTATGTTCTCTC[A/G]CGGAGTCTTCCTGCT | 388795 |
rs540357932 | snp | A/G | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932637 | TTCACTTATACTGGT[A/G]CTCATCTTGCTTTTC | 388795 |
rs540411887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882984 | ACAAGCGTAAGCCAC[C/T]GCGCCTGGCCTAGTT | 388795 |
rs540413980 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869196 | TGTTTGCAAGGCTCA[A/G]GCCAACAACAGGGAG | 388795 |
rs540420817 | snp | A/T | 0.000180424 | 0.00949629 | missense | EFCAB8 | GRCh38.p7 | 20:32875955 | GCCTTCATCAAGGCC[A/T]TGAAGAAGGTTCTGA | 388795 |
rs540469020 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903953 | TCAGGGGTGACTTCA[G/T]TGGAGGGCATACTGT | 388795 |
rs540528978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881842 | CAGATGGGATGAAGG[C/T]GCAATCCACCCCCAT | 388795 |
rs540538070 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904472 | CCCAGCTAATTTTTG[A/T]TTTTTTTGTACAGAT | 388795 |
rs540539526 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887042 | GGGGCTTAGGAGGGT[A/T]CTGGTCCATTGTCTT | 388795 |
rs540564158 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876458 | CTTTTACAGCATCAT[A/C]ATAATAATGCTTTCA | 388795 |
rs540590216 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939849 | ACAGGTGCCCGCCAC[C/T]ATGCCTGGCTAATTT | 388795 |
rs540612369 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946725 | TGAATGCATACAATT[A/G]TGTAATTGGTATCAC | 388795 |
rs540625589 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947059 | ATTTGAGTCATTGTC[A/C]GTTTTGGATGATTAT | 388795 |
rs540641982 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910632 | TCTCTCACTGCCTCA[A/G]GGCTCTTCAGTACCT | 388795 |
rs540704559 | in-del | -/TCAGCC | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902771 | CCTCTGCCTCTGGAG[-/TCAGCC]TCAGCCTCAGCCTCC | 388795 |
rs540778203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868578 | GTGTGATAATACCAC[A/G]GTCTTAGTGGCTTAA | 388795 |
rs540799118 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874612 | AGTGGTGCAATCTCG[A/G]TTCACTGCAACCTCT | 388795 |
rs540809511 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931478 | GAATTAGTATTCGTG[A/G]CCAGTCGTGGTGGCC | 388795 |
rs540810949 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939755 | GCTGGAGTGCAGTGG[C/T]GCCACCTCGGTTCAC | 388795 |
rs540844899 | snp | A/G | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32961542 | TCTCCTCCTTCGAGC[A/G]GCCCCCAAGGCCTCT | 388795 |
rs540871061 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877508 | GCCATTGCACTTGGC[A/G]GTTTTTATTTCTCTT | 388795 |
rs540874563 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944854 | GTTTCTTTTCCTTTT[G/T]AAGATTTGAAACATT | 388795 |
rs540901345 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897401 | TGAATGAATGACGCA[C/G]TCAGGGCGGTCTGGG | 388795 |
rs540938645 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867843 | CAGACATAATAAGCA[-/T]TTTTTTTTTGTTTTT | 388795 |
rs540986161 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923441 | CAGTGAGCTGAGATC[A/G]TGCCACTGCACTCCA | 388795 |
rs541085226 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872881 | CGGATCGCCTGTGGT[C/T]AGGAGTTCGAGACCA | 388795 |
rs541090603 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879678 | AGAGGGGCGATGAGC[A/C]AAGCGTAATACATGG | 388795 |
rs541108309 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860709 | AATTGGCATCATAGT[A/G]TGCACCCTTTTCTGC | 388795 |
rs541153892 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945193 | AGACAGGGTCTTGCT[A/C]TGCCACCCAGGGTTG | 388795 |
rs541171216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953201 | GTATATATATGCCAC[A/G]TTTTCTTTATCCATT | 388795 |
rs541173357 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860177 | GCTGGGCATGGTGGC[A/G]TGCACCTATAATCCC | 388795 |
rs541187794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929124 | AGTGTTCATAAGGGA[C/T]ATTTCTCTGTAGTCT | 388795 |
rs541314434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923095 | AGGCTGAGTTGGGAG[A/G]ATCACTTGAGTCTGG | 388795 |
rs541367020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930189 | AGTGAACAAAAAAGA[C/T]GCAAAATCCCTGCCC | 388795 |
rs541393174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879560 | AGTTTTACATGACAC[A/G]GGAGCCTCTGTAGGA | 388795 |
rs541394955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952623 | AAATTTGGTTGCTTG[C/T]CTTTGTATTCTTGAT | 388795 |
rs541481861 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947114 | TTTCATTTCTGTTGG[A/G]TAAGTATTTAGAAGC | 388795 |
rs541508145 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903172 | CATGTCCTCTCATGC[C/T]CTCTCCTCCTGGCCC | 388795 |
rs541555654 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944329 | AATTAGCCAGGCATG[G/T]TGGTGCATGCCTGTA | 388795 |
rs541566729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911352 | AAAGTGGCTTATGCT[A/G]TAGCAGGGGGCCCTG | 388795 |
rs541607359 | snp | C/T | 8.82184e-05 | 0.00664089 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32878799 | CCTTCCCATGACGGT[C/T]GTCCCCCTGTAAGGA | 388795 |
rs541607858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955320 | CAAGGTGGGAGGATT[A/G]CTTGAACCCAGGAGT | 388795 |
rs541662952 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885442 | GCTCTCTGTTCTGCC[A/G]CAGGTGCCCCCTCCC | 388795 |
rs541683406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880831 | AAGCTTCATGACATC[A/G]GCATTCCTGCCCCTA | 388795 |
rs541781241 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956566 | ACTGGGTATAGAATT[A/C]TCAGCTGGCAGTTTC | 388795 |
rs541828634 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898905 | TTTCTCCTCTGTGAC[C/T]CTCAGTTCCCTCATC | 388795 |
rs541832853 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953412 | CTCCATACTGTTTTC[C/G]ATAGCACATGTACCA | 388795 |
rs541878683 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865253 | GAGGTTCCATTTGAG[C/T]GAGAGTCTGAAGAGT | 388795 |
rs541887087 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917843 | CCATTGCTACTACAC[A/G]TTACCACTGTGGGCT | 388795 |
rs541891791 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901279 | AGAAGAAGAATTGTC[C/T]TGAGTCACACATAAA | 388795 |
rs541895233 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925041 | AGGCTTGGGTGGGCT[-/G]GGGGTAAGGACACCA | 388795 |
rs541935345 | snp | A/G | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860303 | AGAGTGAGACTCTCA[A/G]AAATAAAAGCAAAAA | 388795 |
rs541952972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938083 | ATACTAGCAAATTGA[A/G]ACCAACAACATATGA | 388795 |
rs541953093 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945635 | ATTTTGTTCCTTTGG[G/T]CCATGCTTTCCTATT | 388795 |
rs541953578 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | EFCAB8 | GRCh38.p7 | 20:32962178 | CAGGCTATGGAGTCC[C/T]ATGTGTCCTTCCCCT | 388795 |
rs542059152 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879920 | TGTGCCAGGGGTTGA[C/T]CTGCCTCGCTGTGTG | 388795 |
rs542061702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922705 | AGAGCCTGAAGGAAG[C/T]GAGGAAACATGGCCT | 388795 |
rs542113719 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893802 | CAGCTGAGTCTGGAG[C/T]ACCCCTTGCTGAGCG | 388795 |
rs542124027 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917215 | CTGAGTCGGCTCCCA[G/T]AATCCTCAAGGCTCC | 388795 |
rs542124601 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909783 | GTGAGCAGAGCCCTT[C/G]TGACAGACAAGCTCT | 388795 |
rs542127749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931530 | TTGGGAGGCTGAGGC[A/G]GGTGGATCACGAGGT | 388795 |
rs542163928 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916284 | TTTTTAAGAGACAGG[A/T]TCTTGCTCTATTGCC | 388795 |
rs542171303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928519 | GGATTACAGGCATGA[A/G]CCACCGCACCCAGCC | 388795 |
rs542202747 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960754 | ACACCGAAGGCCATG[C/T]CCCTGCAGGGCCCCC | 388795 |
rs542216715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936264 | GTGTTGAACTCTTGA[C/T]CTCAGGCAATCCGCC | 388795 |
rs542219790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896890 | TGAGTCACCCCGGTA[A/G]CTTCTCATCACATTT | 388795 |
rs542249706 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953312 | TCTATCTCTTTGAGA[C/T]CCTGCTTTCAATTCT | 388795 |
rs542261157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892372 | CGCATCACTGACTAG[A/G]GTTGGGGCCCCCAGA | 388795 |
rs542272539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903246 | GGCTGAAGCCTCACC[C/T]CTCCCCTGGGCTCCC | 388795 |
rs542281298 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895072 | ATCCCTGGGAGGGAA[C/G]CTGAGCCTAGACTGC | 388795 |
rs542287258 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923303 | CCAGCCTGGGCAACA[C/T]GGTGAAACCCCGTCT | 388795 |
rs542291138 | in-del | -/C | 0.039522 | 0.134904 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926655 | CCCAATGCTATCCCT[-/C]CCCCCTCCCCCGACC | 388795 |
rs542295663 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921983 | CATAAGCATGTGCCA[A/C]CATGCCCAGCTGCTT | 388795 |
rs542315570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897973 | CACAGAGTTGGCGCC[A/G]GAGAATTCAGAGCCC | 388795 |
rs542318578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903764 | GGAGATGAAGGAACT[A/G]GCTGGGAGGCTGATA | 388795 |
rs542319014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886014 | CTCCCACGCTGTCCC[C/T]ACGTCCTACCGATTC | 388795 |
rs542332191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929321 | TCAAGCTTTGGGCAC[A/G]AGGGACTTCTGGTTT | 388795 |
rs542345105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937280 | CCACTGCCCACTGCA[C/T]CTAGCTGAAAACCAC | 388795 |
rs542392082 | snp | C/T | 0.000102328 | 0.00715217 | missense | EFCAB8 | GRCh38.p7 | 20:32959926 | CCGTGGGCCGGAGAG[C/T]GCCCCCTGGAAGACA | 388795 |
rs542413271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865346 | GCACCGAATGCTTGC[C/T]GGGCTTGGGGATGGT | 388795 |
rs542432127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879928 | GGGTTGATCTGCCTC[A/G]CTGTGTGTTCCTCCC | 388795 |
rs542461222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901335 | TGAGCTAAATAAAAA[C/T]CACAAAAAAGTCTCA | 388795 |
rs542485863 | snp | C/G | 0.000274738 | 0.0117172 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896411 | GCTTGCCAAGCGAAG[C/G]GGGAAAGCTGCTGAT | 388795 |
rs542503012 | snp | C/G | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32908339 | GTGGGAAGTTTTTTG[C/G]TCTGGGAAACTGCCC | 388795 |
rs542644346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890932 | AACACTGACATCATT[A/G]TGAGGCTAAATTGTG | 388795 |
rs542738719 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914763 | CCTACCAGGTCCCTC[C/G]CTCAACATATGGGGA | 388795 |
rs542797183 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920979 | CCTACTGTACCTTCC[C/T]CTTTCTGACCCTGGA | 388795 |
rs542872628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884016 | GCTGGGATTACAGGC[A/G]TGAGCCACTCTGCCC | 388795 |
rs542903679 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935638 | CAGCCTCCCAAGTAG[G/T]TGGGATTACAGGCAT | 388795 |
rs542981952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934950 | CCCTCCAACATTGTA[C/T]AAGGGTTTTCTTTTT | 388795 |
rs542990013 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911371 | CAGGGGGCCCTGAAC[A/G]TCTGTTTTCTCAGTG | 388795 |
rs543000811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920419 | CTCCTGTATTAATTC[A/G]TTTTCATGCAGCTGA | 388795 |
rs543165822 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922983 | GAGCCCAGGAGTTCT[A/C]GACCAGCTTGGGCAA | 388795 |
rs543181076 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863937 | TTTCTGCATCGGGGA[-/G]GGGGTTGCATACTCA | 388795 |
rs543182777 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884536 | AACCGTGTCCAGACA[A/C]GTTTCCCTTGCTCTT | 388795 |
rs543187912 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958858 | GATTTGCTAGAGCTG[C/G]CTTCCCTGCAGAGAT | 388795 |
rs543188294 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879982 | GCATTGCAGGGGCTC[C/T]GACCTGCTGGGCCTG | 388795 |
rs543189104 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946336 | CTGCTTCACTGAGCC[A/G]GGAGGAGGGATTACA | 388795 |
rs543191304 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898689 | GGTGGTGAGTGGACC[A/G]TGGGGGCTGACAGTG | 388795 |
rs543205831 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897095 | GGCATGTGCTGCGCC[C/T]TCAGGCCGCGGGGCT | 388795 |
rs543242009 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895134 | TCTGACGGAGGACCC[A/C]TGTTTGTCCCTGACG | 388795 |
rs543242706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896597 | CCACTCAAAATAAAT[A/G]CAAAAAGTGGATTTA | 388795 |
rs543357409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922270 | TTGAACATTCTTGCA[C/T]GTACATTTCTGGGCA | 388795 |
rs543420847 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886066 | CAGGAAATCATAGTG[C/G]TTATGAGCATGGGCT | 388795 |
rs543556984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865412 | CTTGAAACTAGAAAG[A/G]TAGGTCAGAGCTGGT | 388795 |
rs543595745 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897162 | CTGTGGTCCCAAGCA[G/T]CCCTCCTAGGACAAC | 388795 |
rs543636736 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870446 | CTCCCCCACCACCCA[A/T]GTGCCCAGGTATGTC | 388795 |
rs543643517 | snp | C/T | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32943673 | CCCTGGTTCCCCCCA[C/T]GCTCCTGATGACCTG | 388795 |
rs543661327 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944579 | TGTATTTTCATATGC[G/T]TTCATGTTCCTGCCT | 388795 |
rs543694129 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923533 | AAATGAAACTTTATA[C/T]GAGTGTATAAAGTAA | 388795 |
rs543701312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929467 | TCTCCCTTCCCTCCC[C/T]TCCCCTCCCCTCCCC | 388795 |
rs543765011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936311 | AGTGCTGGGATTACA[C/T]GTGTGAGCCACCGCG | 388795 |
rs543777689 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950551 | TAAGGATTCAGGGTG[A/G]GAGAATTTATCAGAG | 388795 |
rs543778613 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878304 | TGTGGTGGCTCATGG[G/T]TATAATCCCAGCACT | 388795 |
rs543800065 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885389 | ATGTGCGTGCGTGTG[C/T]GTGACGCTCCGCCGG | 388795 |
rs543851489 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917090 | GTAAGATTAGTTTAT[A/G]TAAAGCCCCTACAAC | 388795 |
rs543866835 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901944 | GCCCGCCTCGGCCTC[C/G]CAAAGTGCTGGGATT | 388795 |
rs543877894 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881707 | GCAAAGCTACTGTAG[C/T]GAGTGCCTCCCCTCA | 388795 |
rs543885201 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859629 | TGTAAGACTACTACA[A/G]AGAACTTCCCTTTGT | 388795 |
rs543920635 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940656 | CTGAAAGAAAATACT[A/T]GCAAATCATATATCT | 388795 |
rs543940048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942762 | TTGTAGGTGTTTTAT[A/G]ATTTCATTGAAAATA | 388795 |
rs543971582 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925719 | AAGGACCAGATGGCA[C/T]GCAGTAGAAAATTGC | 388795 |
rs543973602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884893 | TTGGGTGCAGGGAAG[C/T]AACCCACAGAGGGGA | 388795 |
rs544013142 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934454 | ATTGATATGACATAT[C/T]GATCTCTTTTGGATA | 388795 |
rs544033332 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948987 | TAGAAGAGTAGAGGG[A/C]AATTACAGAAGGAAA | 388795 |
rs544046236 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890046 | ATGCCGCGCTTCCCT[C/G]ATGCCCCCAAAGGCA | 388795 |
rs544054938 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957332 | TTAAAAAAAAAAAAC[A/C]CAAAACTTTTCTGGG | 388795 |
rs544130727 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878159 | TGGTCCCAGCTACTC[A/C]GGAGGCTGAGGTGGG | 388795 |
rs544203023 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887561 | GCCTGGGCGACAGAG[C/T]GAGACTCCGTCTCAA | 388795 |
rs544209763 | snp | A/G | 0.000292697 | 0.0120939 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863879 | AGGGTGGGGCATTCC[A/G]GAGTCACCCAAAACC | 388795 |
rs544216297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895161 | GACGGTGCTGGCTCT[A/G]CTCGTCTGTGTCAGA | 388795 |
rs544231856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924776 | TTGCATGCAAAAGAT[C/T]GAATGTCTATTGGTG | 388795 |
rs544264452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934156 | GCCCTTTCTACTTCT[A/G]TGAGTTTGACTTTTT | 388795 |
rs544272921 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910003 | AGAACCAGACCTCCC[A/T]GTGTGCCTGGGTCTG | 388795 |
rs544276081 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895755 | TTTTGTATTTTTGTA[A/T]AGACAGGGTTTCACT | 388795 |
rs544276385 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889630 | ACAAGCCAGAGGCCA[A/T]ACTGGTCCATCTCTG | 388795 |
rs544276860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919484 | CATAGGTATATTTGC[C/T]CCTCTATCCTTATTT | 388795 |
rs544293586 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888386 | GAGCACCACCACGCC[C/T]AGCTAACTTTTGTAT | 388795 |
rs544334237 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873612 | TCACACCTGTAATCC[C/T]AGCACTTTGGGAGGC | 388795 |
rs544408432 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877390 | ATTTTTGTATTTTTA[G/T]TAGAAACGGGGTTTC | 388795 |
rs544408675 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958210 | AGGCCTGAGCTCCGA[A/G]TGTGTCCTAGGGCTT | 388795 |
rs544420941 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870949 | CTGCAACCTCTGCCT[C/G]CCAGGTTCAAGTGAT | 388795 |
rs544477108 | in-del | -/TT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939157 | TCTTTCTTTCTTTCT[-/TT]CTTTCTTTCTTTCTT | 388795 |
rs544554473 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933472 | CAATTTTTATGGTGA[A/G]ACATTTAAAATTTAC | 388795 |
rs544570590 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888968 | TTTTTTGTGGGGGGC[A/G]GGGGGCGGACAGGGT | 388795 |
rs544576267 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932846 | ATTTGCAATTTTGAT[A/T]GCCTTCTTGCAGTCT | 388795 |
rs544606740 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868251 | AATAATTGTAGAGAC[A/G]AGGTCTTGCTATGTT | 388795 |
rs544657552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943318 | TCAAATGGAATAATG[C/T]GTACAGAGGCACTTG | 388795 |
rs544667587 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911275 | CAGGTCTTCACCAAA[C/T]GTTCCAGTGCGTTCC | 388795 |
rs544674352 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896321 | CACAGTGAGGTGCCA[A/G]TGAGGGTTTGGGTGG | 388795 |
rs544684395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951414 | TAGTGAGAGAAGCCA[A/G]ACGAAAACCTGTACA | 388795 |
rs544707725 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925526 | GCCTAGCTAATTTTG[A/G]GTTTTTAGTGGAGAC | 388795 |
rs544713126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901903 | ATGTTGGCCAGGATG[A/G]TCTTCATCTCTTGAC | 388795 |
rs544719541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920362 | TGGAGAGGATGGAGA[C/T]GCTCAGGATACTGGA | 388795 |
rs544722813 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940981 | AAAGCTGGCCAGGTA[C/T]GGTGGCTCAGGCCTG | 388795 |
rs544729962 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883188 | CCCATTAGAGCATTT[A/C]TCTGATATCACCCAA | 388795 |
rs544794037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947212 | CTACCTTTGTGTCTT[C/T]ATCAACATTTGGTGT | 388795 |
rs544819479 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905066 | CTTCCTGGAACTCCT[C/G]TCTGGGCCTCTCCAG | 388795 |
rs544830005 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946809 | ACTCTATTTCCTTCT[C/G]CTAACCCCTGGCAGC | 388795 |
rs544895808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878028 | CTCACACCTTTAATC[C/T]TAGAACTTTGGCAGA | 388795 |
rs544955893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939928 | TCGAACTCCTGACCT[C/T]AGGTGATCCACTCGC | 388795 |
rs544981946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883903 | ACCACGTTGGCCGGG[C/T]TGGTCTTGAACTCCT | 388795 |
rs544990517 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859506 | CTTTTTTTCCCATTT[A/G]GCGTTTTACCTCTGT | 388795 |
rs544993563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942830 | ATAAAAGATAACAAC[A/G]TAGGTTTCTCTTATA | 388795 |
rs545079699 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890809 | GTGCCTCGCTTTACC[C/G]AGAGGTAAAATGGGG | 388795 |
rs545087600 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914120 | TTGAAATCTAGGTGG[C/T]GGAGGCAGCCATGTC | 388795 |
rs545181579 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864188 | TACCATGTTGGCCAG[G/T]CTGGTCTCAAACTCC | 388795 |
rs545232691 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875086 | GTTTTCTTTGTCTCA[A/G]TCCTTCCTCTTTGTT | 388795 |
rs545252757 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889023 | CAGTGGTGTGTTCAC[A/G]GCTCACTGCGGCAAG | 388795 |
rs545296095 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872867 | GAGGCCGAGGTGGGC[A/G]GATCGCCTGTGGTCA | 388795 |
rs545331761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895089 | TGAGCCTAGACTGCC[C/T]CAGCATTTGTGACCG | 388795 |
rs545346844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926306 | TGACAAAATTTAAAG[C/G]ACATCCTTTAAAATG | 388795 |
rs545375461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925686 | AAGCACTTGCCCCTG[A/G]CCATCTCCCCAGTAG | 388795 |
rs545407772 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | EFCAB8 | GRCh38.p7 | 20:32962248 | CAGCCCTCTTGGCAG[C/T]TGGAGATCCCATTCT | 388795 |
rs545457598 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955894 | GCCTCTTTTAAACAA[A/T]GTATAATTGAGTCTT | 388795 |
rs545509602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919997 | GAGTGCCGCTCTTTT[A/G]TCATCTTCCTCTGGT | 388795 |
rs545517887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877560 | CCTTTAGAACAATGA[A/G]GCCAACTGAAAGAAA | 388795 |
rs545541618 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869902 | TCCTCTGTTTTCAGA[C/T]GTTTAGGTTTTATTG | 388795 |
rs545583114 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940824 | TTAAATGATGGTGAA[C/G]ATCATTAGCTATCAG | 388795 |
rs545585303 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948542 | AGAAAGAAAGAAAGA[A/G]AGAAAGAAAGAAAGA | 388795 |
rs545612055 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899855 | CTGGGATTGCAGGCA[C/T]GAGCCACCGCGCCTG | 388795 |
rs545618741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947440 | TTAATTAAACCGACC[A/G]TATTCTGGTAACAAA | 388795 |
rs545640096 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935447 | TCAAGTGATCTGCCC[A/G]CCTTGGCCTCCCAAA | 388795 |
rs545643723 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | EFCAB8 | GRCh38.p7 | 20:32961758 | GGAAGTTCACCTGTC[C/T]CCTAATCTTGTCTTC | 388795 |
rs545742486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933630 | CTCTCCCTTATTCCC[C/T]ACCCCACCCTCTAAG | 388795 |
rs545744245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941695 | TAGTGGTTTCCTGAG[A/G]CTGGGGGAGGGAGTT | 388795 |
rs545804384 | snp | A/T | 0.000282712 | 0.011886 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875885 | GATGGGCCGAGGGAC[A/T]TGTGAGGAAGGGGAT | 388795 |
rs545805642 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870300 | GTACTGACCTTGGCC[A/G]TCGTTTTTATTGTGT | 388795 |
rs545862501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911783 | TTTGACCCTGGGATG[C/T]ACTATTTTTTGTACC | 388795 |
rs545878225 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945807 | TCTTTTTTGTGGATA[A/C]TTTCACCAGACTTAC | 388795 |
rs545879000 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905992 | TGGGGAAGCTCCTTG[A/C]CTTTTCCTTTTGGTG | 388795 |
rs545890419 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906100 | GCATGGGGACCACAC[A/G]TAGCCAGGGTGGGGC | 388795 |
rs545917570 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905138 | TGGATCGCTGCTTAC[A/T]GAGCTTCCTGCCACC | 388795 |
rs545922501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957189 | TAACATTATTTGTAA[C/T]AGTTATTTAAAGTTT | 388795 |
rs545975512 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930327 | TGGGTGTGGTGACTT[A/G]CTGAGGTCCCTCAGC | 388795 |
rs545999476 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888223 | CATGCACCACCGTGT[A/C]CAGCTAATTTTTTCT | 388795 |
rs546025061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917134 | AAAGCATGTAGTAAG[C/T]GCTTAGTAAATGAGG | 388795 |
rs546060560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938720 | TAAATTTGGAAAAGT[A/G]GTGCAAAACTTGATT | 388795 |
rs546074479 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936219 | TGTATTTTTTGGTAG[A/T]GACAGGATTTCACCA | 388795 |
rs546103870 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924594 | TTATGGCCAGAAAAT[A/G]GCAGAGCCAGGGCCT | 388795 |
rs546118667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882401 | AGAACCCAGCAGCAC[C/T]TCACACAGTTCCGGA | 388795 |
rs546143210 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946435 | TTGTTTGTTTGTTTT[A/T]TCATTCATCTGGGAT | 388795 |
rs546155465 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903935 | AGTGGTGGAGGAGCC[A/G]GGTCAGGGGTGACTT | 388795 |
rs546166856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861409 | TTCTCCTGCCTCAGC[C/T]TCCTGAGTAGCTGGG | 388795 |
rs546191964 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875051 | ACCGTGCCTGGCCTG[G/T]TTCTCCTTTTCTTTG | 388795 |
rs546204522 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904455 | GCAGGTGCACCATCA[C/T]GCCCAGCTAATTTTT | 388795 |
rs546213034 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892989 | GGGATTACTGGTGCC[C/T]GCCACCACGCTTGGC | 388795 |
rs546274120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887294 | AAGAGTAAAATACAG[C/T]GCCAGGCGCGGAGGC | 388795 |
rs546276109 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893508 | CACGAGGGCTGGGGA[G/T]AGGGGTGGCCTCTCT | 388795 |
rs546305743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930965 | GTGCTGTCCTTGAGC[C/T]GGTCACACCCTTCCT | 388795 |
rs546338581 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874392 | TACACCTGGCTAATT[A/T]AAAAAATTTTTTTTG | 388795 |
rs546354974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953573 | CAGTTCTCTAATGAT[C/T]CATGAGGTTGGCAAT | 388795 |
rs546359563 | in-del | -/CTTTTTT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935192 | TTTCTTTCTTTCTTT[-/CTTTTTT]TTTTTTTTTTTTTTT | 388795 |
rs546379701 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880510 | TTGGGGCCTCAAGTA[A/C]TCCGCTCACCTTGGC | 388795 |
rs546380741 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867022 | TCCTGGGTTCGAGTG[A/C]TTCTCCTGCCTCAGC | 388795 |
rs546395834 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960770 | CCCTGCAGGGCCCCC[C/G/T]TGTCTCGGGCTGGGG | 388795 |
rs546399124 | snp | A/G | 0.000798403 | 0.0199641 | missense | EFCAB8 | GRCh38.p7 | 20:32961209 | CTGACTTCCTGACCA[A/G]CAGGGGCCCAGACCA | 388795 |
rs546419365 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861537 | CAGGTGATCCGTCTG[C/T]CTCGGCCTCCCAAAG | 388795 |
rs546429623 | snp | C/T | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860478 | GTCATTTTGTTCCAT[C/T]GCTGATGGTGGTAAC | 388795 |
rs546483094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868250 | TAATAATTGTAGAGA[C/T]GAGGTCTTGCTATGT | 388795 |
rs546524555 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860886 | TGGGACTACAGGGGA[G/T]TGTCACCATACCCAG | 388795 |
rs546544718 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889175 | TCACTAGACTTAGTG[A/G]TAGTGCTAGGCTCCA | 388795 |
rs546545552 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923634 | TTTTTTTGTGCATAT[A/G]CAAGTACATACATGT | 388795 |
rs546547086 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940175 | CCCAAGTTCAAAACT[A/G]AATATGAAGTTAAGT | 388795 |
rs546570463 | snp | A/G | 0.000100296 | 0.00708081 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867765 | AAGGCCGCTCTGTAG[A/G]CTCGGTTTTTGTGTG | 388795 |
rs546645867 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32961349 | TCCCCATCTTCCTTG[C/T]TATCTGTCACTGCCT | 388795 |
rs546649376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888645 | ACAGGCGTGAGCCAC[C/T]GTGCCCTTTTCTTTT | 388795 |
rs546681766 | in-del | -/TTGTTG | 0.00478085 | 0.0486577 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882692 | CGCCTGGCCGATTTT[-/TTGTTG]TTGTTGTTGTTGTTT | 388795 |
rs546709769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924956 | ACAGTGAAGCATTTT[A/G]GGGTGGTGCCCTGGA | 388795 |
rs546721253 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924106 | TTGTCCAGGCTGGAG[C/T]GCAGTGGCACAATCA | 388795 |
rs546743308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875109 | TCTTTGTTAATTGTA[C/T]GGAAATGGGAGTTGG | 388795 |
rs546847252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937655 | ACAGAGTCTCACTCT[A/G]TTGCCCAGGCTGGAG | 388795 |
rs546887799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945245 | CTCACTGAAGCCTTG[A/G]CCTCCCAGCCTCAAG | 388795 |
rs546921274 | snp | C/T | 0.000273311 | 0.0116868 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32930475 | GGACGGCTACATCTA[C/T]GCCTGGTCCCTCCAT | 388795 |
rs546926760 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897601 | GCACCACACCCAGCT[A/T]ATTTTTTAATTCTTT | 388795 |
rs546937973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904762 | CTCCTGAGTAGCTGG[A/G]ATTACAGGCACATAC | 388795 |
rs546947726 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909493 | CTCGCCTGGGGCAAG[G/T]GGGAGGCAGGGAGGG | 388795 |
rs547014122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881188 | CTAAGAGACAATGTC[A/G]TCTCTCTTTTCTTTT | 388795 |
rs547039709 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880705 | CAAAGGATACAGATG[A/C]ACAGATGTGTAGGGC | 388795 |
rs547052811 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887313 | AGGCGCGGAGGCTCA[C/T]GCCTGTAATCCCAGC | 388795 |
rs547071859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866535 | GGAAGGCTTCTGGGG[A/G]GATTTGGGAAGGATG | 388795 |
rs547081985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873010 | GGCAGGGAGAATTGC[C/T]TGAACCCAGGATGCG | 388795 |
rs547108490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909985 | CACCAGGTGACACGG[A/G]GCAGAACCAGACCTC | 388795 |
rs547114170 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902878 | CAAATCTGACGGAGC[A/G]GGTGTGGTAGCAGGA | 388795 |
rs547142002 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945875 | TTTTTTTCAGGAGTC[A/C]ATTATCTCTTGCTCT | 388795 |
rs547224527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885713 | GCACCCCCATGGTGA[A/G]GGTGACCTGGAGCCA | 388795 |
rs547232451 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860977 | ATTCCTGGGCTCAAG[C/T]GATCTTCCCACCTTG | 388795 |
rs547247206 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927108 | AAAATGCACAAAATT[A/G]TAAAAAATTAGGTAC | 388795 |
rs547255562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879682 | GGGCGATGAGCCAAG[C/T]GTAATACATGGCGGA | 388795 |
rs547310504 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950864 | GTAGTTAGAAGAGAC[A/G]TGATTTCCTTGAAAT | 388795 |
rs547316892 | in-del | -/TTTTG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900359 | ATGTCCAGTGCCTTT[-/TTTTG]TTTTGTTTTGTTTTG | 388795 |
rs547328973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916471 | GCTCTGTTGCCCAAG[C/T]TGGTCTTGAACTCCT | 388795 |
rs547340861 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895952 | TACAGGTGTGAGCCA[C/T]TGCGCCTGGCCCAGA | 388795 |
rs547347611 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920476 | AAAAGAGGTTTAACT[A/G]GACTTATAGTTCCAT | 388795 |
rs547398503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952964 | TTTATAGTCATTGAA[C/T]ATACTCCTCCATTTC | 388795 |
rs547402426 | snp | G/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960850 | CTCACCCAGGGTCCA[G/T]CTCGAGGCCTCATTC | 388795 |
rs547407751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865503 | AAGTCATTGATCAGA[C/T]TTGCTGCCTAGAAGC | 388795 |
rs547490637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951816 | GCAATGCCTGTTCAG[A/G]TCTTTTGCCATTAAA | 388795 |
rs547544774 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891136 | TATTTTTTTGAGACA[C/G]TCTCACTCTGTCACC | 388795 |
rs547569507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959002 | GCTGGCTACTTGGTC[C/T]TCCCCCTGCAGGTTC | 388795 |
rs547580847 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954630 | TCTTAGATTTCCCTC[C/T]AGAAACTAGAGATTT | 388795 |
rs547582870 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896672 | CAGGTTGCGGCAGCT[C/G]TTGGATCCCGTCAGC | 388795 |
rs547621116 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928714 | TATTTCTTTTTTTGC[C/G]TAATCCCTCTGGCAG | 388795 |
rs547633418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914442 | ACTAATCTCATCAAA[C/T]AGTGCTTGGCTATGT | 388795 |
rs547638951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959464 | AAGGCAGGGTTTCCC[C/T]GGGGCAGGGGGCAGA | 388795 |
rs547651670 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873820 | CTGTCCAAAAAAAAA[A/T]AAAATGCAGTTCACC | 388795 |
rs547713716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865004 | CTGTGGCTCAGGGAA[A/G]TGATGTGATATGCCT | 388795 |
rs547777234 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943138 | TTGCTCACCCTATTC[A/C]TCTCCCAATACCCAG | 388795 |
rs547856182 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921937 | TGAGTTCAAGTGATT[C/T]TCCTGCCTCAGCCTC | 388795 |
rs547920661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903510 | GGTAATCCTGGCAGG[A/G]GTAGGAGCCAGGAAA | 388795 |
rs547964773 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951168 | GTTAAATGTGCCCCT[A/G]TGATATGAATCAGCT | 388795 |
rs547966508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907574 | TTAGGGGACAGGTTA[C/T]GTTTTCTGGAACTCT | 388795 |
rs548030326 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904728 | ACCTCCCAGGTCCAG[A/G]TGATTCTCCTGCGTC | 388795 |
rs548044020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873940 | TTTATTTATTTATTG[A/G]GACAGGGTCTTACTC | 388795 |
rs548097013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908600 | CTGTTTCTAGGCCCC[C/T]AGCCTGTCACCCTCT | 388795 |
rs548115204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951042 | AAAACCGCTGTAAGA[C/T]ACCATTTATCTTATT | 388795 |
rs548129228 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907925 | CACTACCGGACTGTG[G/T]CCCAGGCTGGAGTGG | 388795 |
rs548145370 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960915 | GTTGCCACAAGCGCC[A/G]TAACTGGGTGGAGAG | 388795 |
rs548190291 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944452 | CCTGGGCAACAGAGT[A/G]AGACTCTGTCTAAAA | 388795 |
rs548192983 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954498 | TTATATGTCTGTTTT[A/T]ATGCCTGTACCACAC | 388795 |
rs548193229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945353 | GTAGAGACAGAGTTT[C/T]ACCATGTTGCCCAGG | 388795 |
rs548194615 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867575 | GTTCTTGTTATATTC[G/T]TTCCAGCTGTCCATC | 388795 |
rs548195938 | snp | A/C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954187 | TTTTTAGTGTCATAT[A/C/T]CAAGAAATAATGGCC | 388795 |
rs548210511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910592 | ATTCTGGGCTTCTCT[C/T]CCATCCTGGCTCCTG | 388795 |
rs548230107 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953781 | CTGTAGGCTTCGTTT[A/T]CATTGGGTTGATTGT | 388795 |
rs548260699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936581 | CTGTCTTTTCCCCAT[C/T]ATGTATTAGTAACAC | 388795 |
rs548264558 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876182 | TGGCCCCAGTCGGGG[G/T]ACTTGCCTGGTGGAG | 388795 |
rs548343024 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886227 | TTACAGTCCTTTTGG[A/G]AACACATGATGACAT | 388795 |
rs548361473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951953 | TGTGTTTACATTCTC[C/T]TCATAGTGCATTTTG | 388795 |
rs548377737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886629 | CATCCTGAGGCTGTG[A/G]CTTCCATAGCCATCC | 388795 |
rs548399521 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889511 | GAACATGGATCAGAG[C/T]CCCCTGGGAGGATAG | 388795 |
rs548429101 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929628 | ATTACAGGTATGAGC[C/T]ACCATGAGATTTTTG | 388795 |
rs548487819 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865659 | AAAAAATTAGCCAGG[C/G]GTGGTGACTCATGCC | 388795 |
rs548518034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943887 | GCTGGTATGAACTTT[A/G]TACTCTGTGGGGAGG | 388795 |
rs548519950 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952693 | CAGGTATCCACATTG[C/T]GAGTACTTTTATCAG | 388795 |
rs548521089 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959517 | GGAGGTCCAGATAAA[C/G]CCAGATCGGGTGTCA | 388795 |
rs548523682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920828 | TCTGGATTGGGGGTA[A/G]CAGTGTCCCCTCTGG | 388795 |
rs548541794 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908646 | CTGTCTGCACTGTCC[C/T]CACTCAGGCGTCCTC | 388795 |
rs548578335 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860277 | TGAGCCACTGCATTC[C/T]AGCCTGTGACAGAGT | 388795 |
rs548579031 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899651 | GCGATCTCGGCTCGC[C/T]ACAACCTCTGCCTCC | 388795 |
rs548627044 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859887 | CACCAAATAACAGCC[C/G]TTGCAGCATTTTTGT | 388795 |
rs548640426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897637 | AGACGGGGCCTCACT[A/G]TGTTGCCCAGGCTGG | 388795 |
rs548685539 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921573 | GTAATAATACTAGTT[G/T]ATAATAAAAAAGGAA | 388795 |
rs548688078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947712 | AAAAACAGTAGTAAC[A/G]GGGAAATTTGTAGCA | 388795 |
rs548725023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922442 | ATTCGCTACATGCCA[A/G]CCGCTGGGGAAGGAG | 388795 |
rs548857673 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927805 | TGGTTCAGGGATTCC[G/T]GTTTTTTCTTTTTTT | 388795 |
rs548895011 | snp | C/G | 0.0399052 | 0.1355 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926915 | CAGTCTATCATTGTT[C/G]GACATTTGGGTTGGT | 388795 |
rs548967360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873237 | CCTCCTTAGACAGAC[C/T]CTAGGAAGGCTTCCC | 388795 |
rs549007479 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906667 | AGAAGCTGCTGGGGG[G/T]AGGGCTGCTGGGGAT | 388795 |
rs549041582 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935161 | CTTTCTCCATTTTCT[C/G]TTCTCTTCTCTTTTC | 388795 |
rs549062318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871960 | GTCTGGAAGGAGGCC[A/G]CAGGGCTCATGGCCT | 388795 |
rs549062517 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878891 | AGCCCCTCCCTCAAT[C/G]CGTGACCTTGCTGGT | 388795 |
rs549142670 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876245 | CCTGGCAGCTCATTC[C/T]CCAGGGACAAGTGTC | 388795 |
rs549144318 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893522 | AGAGGGGTGGCCTCT[C/G]TGAGGATGGGAGGCT | 388795 |
rs549163169 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883352 | TTGCCGGGAGGCGCT[C/T]ACAGGCTTTTGTCGT | 388795 |
rs549172062 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942318 | CTTTGTATAACTTTA[G/T]GAATTGTCTCTTCAT | 388795 |
rs549201766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882883 | TGCATTTTTAGTAGA[A/G]ACGGGGTTTCACCAT | 388795 |
rs549226419 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914931 | AGACATGGGATCTCA[C/T]TCTGTCACCCAGGCT | 388795 |
rs549236863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864290 | TAAGTGTACTTTTAA[A/G]GGGCTGCCTGAGACT | 388795 |
rs549267514 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919012 | AGACACAGACAAACC[A/T]CTTTCCTCCTCCTCT | 388795 |
rs549273006 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884488 | TTCATCACAATCTAC[C/G]CAGAGCCATGGGCTG | 388795 |
rs549326534 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915158 | TCCTCCTGTCTTGGC[C/T]TCCCAAAGTACTGGG | 388795 |
rs549360460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870524 | TTTTTTTAGGGACAG[A/G]GTCTCGCTTGGTTGC | 388795 |
rs549385839 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958297 | GGGCACTCAACATTT[G/T]AGTGAGTGTGGGGGC | 388795 |
rs549422690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957564 | TTCAGTGGGACTCTG[C/T]CTCCCAATGATCTCA | 388795 |
rs549479364 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915752 | TCTTGGCTCACTGCA[G/T]CCTCCGCGTCCCGGG | 388795 |
rs549520504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879018 | TCCCCATTTTATAGA[C/T]GAGGCCACTGAGGTC | 388795 |
rs549556901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891005 | ATCTATCTGTGACCC[A/G]CCTGGGCTTTCCACT | 388795 |
rs549593131 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891367 | GGATTACAGGTGCGC[A/G]CTACCACACCCAGCA | 388795 |
rs549593932 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950572 | TTTATCAGAGGCTTG[A/G]ACTGCTTCTGTGTCT | 388795 |
rs549630457 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941721 | GAGTTGGGGAAATTG[C/T]GTAGTGACTACTGGG | 388795 |
rs549656881 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947838 | TTTGGGAGGCAGGTG[A/G]GAGGATCATTTGAAC | 388795 |
rs549667188 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922356 | CCATCTCTTTAAATC[G/T]GTGAAGTCAAGGTAG | 388795 |
rs549706697 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866330 | ACTTCCCAAGGCCCA[A/G]AGCAATGTGTCTCAG | 388795 |
rs549738300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959645 | GTGATGGACTCTGGG[A/G]AGTCTGGCCTGAGGG | 388795 |
rs549739772 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924305 | CTGGGCTCAAGCGAT[C/T]CTCCTGCCTTGGCCT | 388795 |
rs549762600 | snp | A/G | 9.33315e-05 | 0.00683059 | missense | EFCAB8 | GRCh38.p7 | 20:32885638 | CTGATGAGCTCCTTT[A/G]GGGTGAGTGGGGCCC | 388795 |
rs549803646 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952034 | GGGGGCCAAAGTGGG[G/T]GGATTGCTTGAGCTC | 388795 |
rs549805481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921593 | TAAAAAAGGAAGTGT[A/G]TGTAAATGAAAAAAT | 388795 |
rs549844120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928572 | TGACTTTGTATCCTG[C/T]CATTTTGCTGAATTC | 388795 |
rs549845208 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877699 | CTTTGGGCCTTGGCC[-/A]TGTTTTCCAGCAGCT | 388795 |
rs549866244 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895627 | CCCAGGCTGGAGTGC[A/C]ATGGTGCGATCTTGG | 388795 |
rs549884921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950986 | ATAGAAGCATGGAAA[A/G]CAATGCGCAATATTT | 388795 |
rs549937189 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872968 | GTGATGGTGGGCGCC[A/T]GTAATCCCAGCTACT | 388795 |
rs549938899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885157 | GGGCAGTTTTTCCTA[C/T]GATAGAAGCTTTGCG | 388795 |
rs549946243 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907884 | TCTGGGGACAGGCAG[A/G]CCACTGTGGCAACTA | 388795 |
rs549960310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870702 | AGATGGGGTCTTGCT[A/G]TGTTGCCCAGGCTAG | 388795 |
rs549972441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877100 | TTCAAACCAGGGAGG[A/G]TGCCTTGAGAGTCCC | 388795 |
rs550002098 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935269 | GCATTGATCCAATCT[G/T]GGCTCACTGCAACCC | 388795 |
rs550010501 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895458 | GCCTCCCAAGTAGCT[A/G]GGACCACAGGCACGC | 388795 |
rs550011818 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901493 | TTTTATTGAGTCCTG[A/C]TGGCAGGAGGATATC | 388795 |
rs550021202 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878579 | GCGGACTGCAGTGGC[A/G]CAATCTCGGCTCACT | 388795 |
rs550086748 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920948 | ACGAGTTGGGTATGG[A/G]TTCATCTTTGTTCTT | 388795 |
rs550096471 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871126 | CAAAGTTCTGGGATT[A/T]CAGGTGTGAGCCACC | 388795 |
rs550122387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884103 | TGAAACAGAATGTCA[A/G]GAGGCTTGTTCCTAT | 388795 |
rs550162252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950150 | GTTTGCATGCAACAC[C/T]GATAGAGCATGATTC | 388795 |
rs550165539 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875283 | CGGAATTGGCCTAGC[C/T]TGGGGTGGCTGGGGT | 388795 |
rs550190867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900863 | GTGAGCCACCATGCC[C/T]GGCTTAATTTTTGTA | 388795 |
rs550222740 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918645 | ACACACCGTCTGTGT[A/G]TGTGTTTTCTTATTG | 388795 |
rs550334776 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888779 | GTTCTTAATGTCTGG[C/G]TGGTGTCCATGGTGT | 388795 |
rs550337812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947914 | CAATTAAAAAAAAAA[A/G]AAAAGAAAAAAGAAA | 388795 |
rs550348488 | snp | A/G | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32920165 | GATGAAACGAGAAAA[A/G]GAGAATGGCAGAAGA | 388795 |
rs550350296 | snp | C/T | 0.000445494 | 0.0149181 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32912811 | TAGTGGGATTATCCA[C/T]ATGAACAAAGTGTTC | 388795 |
rs550389525 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900273 | ACAGATGGGAAACCC[A/G]AAGCTTAGGGAGGGG | 388795 |
rs550426953 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907266 | TCCCTATCCATAGAA[C/T]GGGCTGTTGAGTGGT | 388795 |
rs550514108 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918109 | AATATTTGGAAACCA[C/G]TGTCCATTTTACAGA | 388795 |
rs550537997 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866159 | CACAGTGCTGTATCC[A/G]CAGTGCCTAGCACTC | 388795 |
rs550540130 | snp | C/T | 0.000552384 | 0.0166098 | missense | EFCAB8 | GRCh38.p7 | 20:32889332 | AGCTCTACAACCAGC[C/T]GATGTGGGTCATTGA | 388795 |
rs550582598 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890897 | TGGCATAGTGCCTGG[A/C]ACATAGTGGGCAGTT | 388795 |
rs550621839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894715 | CAAATAGGGATGGCC[C/T]TACTTCCCTGATAGC | 388795 |
rs550675576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918686 | TTTCCAAAGTGCCTT[C/T]AGGTCCCTCAACTCA | 388795 |
rs550683441 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919706 | GTTTCACCATGTTGG[C/G]CAGGCTGGTCTCAGA | 388795 |
rs550749299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893615 | CCTGGGGAAGTCCTT[C/T]ATCCACTCTGATCCT | 388795 |
rs550750564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955464 | AGGATCGCTAGAGCC[C/T]AGGTGTTTGAGGTTG | 388795 |
rs550818983 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869512 | AAGTGCTGGGATTAC[A/C]GGCGTGAGCTGCTGT | 388795 |
rs550869196 | snp | A/C | 0.000208095 | 0.0101982 | missense | EFCAB8 | GRCh38.p7 | 20:32931299 | CTCAGCAACTTGGGA[A/C]CAACTTCCCACACTA | 388795 |
rs550885436 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887402 | CCACCATGGTGAAAC[C/T]CCGTCTCTACTGAAA | 388795 |
rs550888238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923715 | TGCATGTATTATTCC[A/G]GGACTTGCTGTTTTT | 388795 |
rs550890272 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923748 | CTTGACTCCTCACGG[A/G]CATCTCTTCATGACG | 388795 |
rs550900753 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899423 | AAAAAAAAAAAAAAG[A/G]AAAACCAATTAATCA | 388795 |
rs550906066 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938466 | TTAGGCAAGAAAATG[A/T]AATAAAAAGTATCTA | 388795 |
rs550933040 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926757 | TGAGTGAGAATATGC[A/G]GTGTTTGGTTTTTTG | 388795 |
rs550965995 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934566 | TGGTTGATATGGTTT[G/T]GTTGTGTCCCCACAC | 388795 |
rs550966805 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881945 | AGGCATGGTGGCTCA[A/C]ACCTGTAATCCCAGC | 388795 |
rs551030089 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912147 | ACCAACTCAGAAAGT[A/G]TACTTAGCTGGCCAG | 388795 |
rs551036395 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951599 | AGAAGCAGGAAGAAA[-/C]TTTTGCAGGTGATGG | 388795 |
rs551131711 | snp | A/G | 0.000443086 | 0.0148777 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876070 | TGCCCCTGCTTCCTC[A/G]GGTGCTGGAGGGAGG | 388795 |
rs551131960 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869083 | TGTTGGCAGAATTCA[C/G]TTCCTTGCCCCTGTG | 388795 |
rs551171092 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946407 | GTTTTTTGTTTTTTG[-/T]TTTTTTTGGTTTTTG | 388795 |
rs551182060 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935157 | GATGCTTTCTCCATT[G/T]TCTCTTCTCTTCTCT | 388795 |
rs551206845 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888077 | TTTTCTTTCTTTTTT[G/T]TTTTGAGACTGGGTC | 388795 |
rs551243757 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | EFCAB8 | GRCh38.p7 | 20:32961661 | AACCAGGCCCATGGC[A/G]GTCCTGCATGTTCTC | 388795 |
rs551292785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932005 | TGGAAGGAATCATGA[A/G]GGGGACTTCTGGAGA | 388795 |
rs551305495 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933804 | GCCCACATGGTGAAA[A/C]CTTGTCCCTACTAAA | 388795 |
rs551357726 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895264 | CCCATGAGGGCTGCA[C/G]CTGGCTTGCCTGAAT | 388795 |
rs551377750 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864367 | GGCAGGAGGATCGCT[A/G]AGCCCAGGAGTTTGA | 388795 |
rs551394589 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900728 | TGCGCCACCATGCCC[A/G]GTTAATTTTTTTTCA | 388795 |
rs551423829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877852 | AGGGGAGAGTGAATA[A/G]AGAGCTCCCAGGGTG | 388795 |
rs551428845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883682 | AATAAGGTCAAGCCT[C/T]CACTGGTCTATTTCT | 388795 |
rs551445755 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919574 | TGGTCTTCGCTCAGT[G/T]CAACCTCTGTCTCCT | 388795 |
rs551448487 | snp | A/G | 0.000460681 | 0.01517 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906558 | CACTCCTTTGATATT[A/G]TAGGTTGTCAGTGCT | 388795 |
rs551450307 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913585 | AGTCTTAACTTGTTC[C/G]AGTATCAACTTTAAT | 388795 |
rs551453025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884938 | ATGAATGCTCAAGGG[C/T]GGCCTCCTGCGAGGC | 388795 |
rs551484012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912651 | TGAGAACATGATGAC[A/G]AATACATGGTGGTAT | 388795 |
rs551484029 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905647 | TACCTGTAATCCCAG[A/C]TACTCTGGAGGCTGA | 388795 |
rs551488907 | snp | C/T | 0.000102664 | 0.0071639 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920258 | ATATGAGCTGGGGAG[C/T]GGGCGGTCAGGATTG | 388795 |
rs551534172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941183 | CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 388795 |
rs551550662 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888061 | TCTCTACATATCCCC[C/T]TTTTCTTTCTTTTTT | 388795 |
rs551565335 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899515 | AGTCCTGAGGGGCCC[C/G]CTCCTTATTCAATCG | 388795 |
rs551570066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949213 | TAAAAGATACATTTA[C/T]GAAAACATAAAACAT | 388795 |
rs551588819 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939300 | TTTTGTTTTTTGTTT[C/T]TTGACAGAGTCTTGC | 388795 |
rs551590947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888133 | GAGTGGTGCAATCAC[A/G]GCTCACTGCAGCCTC | 388795 |
rs551596532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900158 | GGGCAGAAACAGAGG[A/G]CCATTTAGACCCATG | 388795 |
rs551598574 | in-del | -/T | 0.346147 | 0.230772 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888070 | TCCCCCTTTTCTTTC[-/T]TTTTTTTTTTTGAGA | 388795 |
rs551615178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870367 | TTCAATATATCCAAA[C/T]GGTTCAAAATCCAAA | 388795 |
rs551654124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924321 | CTCCTGCCTTGGCCT[C/T]CCAAAGTGCTGGGAT | 388795 |
rs551672968 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889433 | GGGGCTTCCCAGCTC[G/T]GCTCTCAGCCACTGG | 388795 |
rs551774287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861613 | CATGTTAAAGATTGC[C/T]ATGAGCCTGGTGTGG | 388795 |
rs551853361 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957492 | TTAGGAGGACTCAGT[G/T]TGCCTCTGTGTTCAG | 388795 |
rs551935057 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953413 | TCCATACTGTTTTCC[A/G]TAGCACATGTACCAT | 388795 |
rs551949598 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867322 | AGTAAGGTAGGACTT[C/G]GCTGTATCCTCCCTG | 388795 |
rs551970364 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932927 | GTATGAAGAGAATGT[C/T]ATTATATTAAAATGT | 388795 |
rs551979284 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929802 | CCTGCTGGGTGCCAG[A/G]CAAGAAACTTTCTTC | 388795 |
rs551980128 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32961046 | TGGGAAGACCTCAGG[A/G]CGCCTCCTTCCTGTG | 388795 |
rs551981623 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912175 | CAGGCAGTGGCTCAC[A/G]CCTGTAATCTCAGCA | 388795 |
rs552007185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932101 | ATTCAGTGGTGGGCC[A/G]GGCACGGTGGCTCAT | 388795 |
rs552049064 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918869 | AACCCTGAAAACCTA[A/C]AATTGGATGTTAGAT | 388795 |
rs552086466 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924821 | GTGGCTGGCAGGGCT[A/G]TGTGTGTGTGTGTGT | 388795 |
rs552087777 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868088 | TGCTATTAAAAGTAA[A/T]GGCAGAAATCACAAT | 388795 |
rs552093560 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874045 | CCCAGCTCAACCTCC[A/C]CAGTAGTTGGGACTA | 388795 |
rs552142407 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908610 | GCCCCCAGCCTGTCA[A/C]CCTCTCTGCAGCTGC | 388795 |
rs552168407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955374 | GTGAGACCCTGTCTC[C/T]ACAAAAAATTAAAAA | 388795 |
rs552173316 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904190 | TACAGATGGGATCTT[C/G]CTGTGTTGCCCAGGC | 388795 |
rs552180514 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932254 | TGGCGGTGCACGCCT[G/T]TAATCCCAGCTACTT | 388795 |
rs552204004 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934328 | ATTATGTATATACAC[A/C]ACATTTGCATTATCC | 388795 |
rs552253169 | snp | C/T | 0.000359518 | 0.0134026 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930376 | ACAGCCCTGCTGAGC[C/T]GGGCCCTCCTCTCTT | 388795 |
rs552258169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898781 | ACGGTGAGAACACAG[C/T]AGCCTCTTTTATCTC | 388795 |
rs552343779 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939382 | CCGCCTCCCAGGTTC[A/C]AACGATTTTCCTGCC | 388795 |
rs552344545 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874980 | TCTCGAACTCCTAGC[C/T]TCAGGTGATCTTCCC | 388795 |
rs552362496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910157 | GTTAGCCATGGGATC[A/G]CCTAACTCCTCTGAG | 388795 |
rs552362567 | snp | A/T | 0.000110102 | 0.00741881 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917286 | CAGCCCTCCTGCCTC[A/T]GGCCATATGCACAGG | 388795 |
rs552489319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945068 | GTCTGCTGATTTTTC[C/T]TTCTGCTTGATCAAG | 388795 |
rs552509124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952834 | TTGTGGTAAAATATA[C/T]AGCATAAAACTTACC | 388795 |
rs552522644 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910675 | TTTAAAATTTAAAAA[A/C]ATTATCAACTTTTCT | 388795 |
rs552537087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902785 | AGTCAGCCTCAGCCT[C/T]CAAGGCAGTGTGGGC | 388795 |
rs552545081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929692 | TGGGGACACATAAGC[C/T]ATTACACTGTAAAGT | 388795 |
rs552589394 | snp | G/T | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860279 | AGCCACTGCATTCCA[G/T]CCTGTGACAGAGTGA | 388795 |
rs552600320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900079 | AGGAGAGTCTTTTTG[A/G]GGGAACAGCAGGAGA | 388795 |
rs552624478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882302 | TCCAAACAGAATATC[A/G]TCCATTCACTTTGAA | 388795 |
rs552640095 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923626 | TTCTAGAATTTTTTT[G/T]TGCATATACAAGTAC | 388795 |
rs552663104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881654 | TCCTTTGCAAGGGAC[A/G]TCGGGTTCAGCCACT | 388795 |
rs552757296 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859936 | AATTCAGAATCGTGC[A/G]TTGCCTTTAGTTGTT | 388795 |
rs552773158 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880761 | GCTTCAGGAACCTCC[A/G]TGTGTTCAGCCATAG | 388795 |
rs552774866 | in-del | -/TCT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921197 | TTCTGATTATTTCTC[-/TCT]CCTTTTTTTTTCTTG | 388795 |
rs552878314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938045 | CAAATATTTTTATGA[A/G]TATAGATACAAAAAT | 388795 |
rs552943411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32961096 | GTGTCCCCGGCTCCA[A/G]CTGGTGCCCCATTCC | 388795 |
rs552947623 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953271 | CTGTTGTGAATTGTG[C/T]TTCTGTGAACATGGG | 388795 |
rs552975125 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932307 | ACTTGAACCCGGGAG[G/T]TGGAGGTTGCAGTGA | 388795 |
rs552981678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887570 | ACAGAGCGAGACTCC[A/G]TCTCAATAAAAAGAG | 388795 |
rs552982172 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960736 | TTAAGAATAAATGAG[A/T]TAACACCGAAGGCCA | 388795 |
rs553024524 | snp | C/T | 0.0001844 | 0.00960031 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32918415 | GCCCAGCAGACCCTA[C/T]GTGGAGCGGGAGAAG | 388795 |
rs553046048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909749 | ATTTATTGGAAGTTT[C/T]TCCCGGCAGCCCATC | 388795 |
rs553064712 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906068 | AGATGTCCAGATGAT[A/G]CAGGAGACAGCACCC | 388795 |
rs553068330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866926 | TCTTTCGTTTCTTTC[A/G]TTTCTTTTTTTTTTG | 388795 |
rs553126420 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903312 | TGCCCTGGACCCTCC[C/T]CAGAGAGGCCGGCAG | 388795 |
rs553165981 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955870 | CCATCTCTGTTCTTA[C/T]ATTTGTGTGCCTCTT | 388795 |
rs553218586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893399 | ACTCCCTGCCTCTGC[C/T]CTGGAGTCTCTGGGA | 388795 |
rs553244714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897908 | GCCTTTTCCATTCTC[A/G]TCACAGAGAGGAAAA | 388795 |
rs553245694 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923304 | CAGCCTGGGCAACAC[A/G]GTGAAACCCCGTCTC | 388795 |
rs553282449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922671 | AGGGAGGGCTTCACA[A/G]AGGAGGTGGCATCTG | 388795 |
rs553288067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917008 | TAAGGCCACAATGTC[C/T]CCCCCCCTTTAAACC | 388795 |
rs553313069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902260 | GGTGAACACACCAGT[A/G]AGGAGGCCATTGCAA | 388795 |
rs553383883 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916107 | GTAGGTGGCTTATAA[C/T]AACAGAAAATTATTT | 388795 |
rs553390035 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954892 | AGTAAACCCCACTTA[A/G]TCAAGATGTATTATT | 388795 |
rs553394756 | snp | A/G | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32867708 | ATACACCTGGCCAAG[A/G]TAGAGAAAATGTTTG | 388795 |
rs553444392 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880380 | TTCAAGCGATTCTCC[C/T]GCCTCAGCGTCCCAA | 388795 |
rs553448423 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946312 | GGAAGCTGGTGGTTC[C/T]TTCCCAATCTGCTTC | 388795 |
rs553471955 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944120 | CATACAAACCAGAAG[G/T]GTTCAGCTTGGTGAA | 388795 |
rs553578428 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891732 | AGAGGCAGAGGAGGG[C/T]GAGAGGCTGCCGTTC | 388795 |
rs553637798 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930064 | GAGTTACAGGTTGTG[-/A]AAATCTTGTCTGAGC | 388795 |
rs553652052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886005 | GGTCAGCCACTCCCA[C/T]GCTGTCCCCACGTCC | 388795 |
rs553654346 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879886 | GTAGCATCTCTCAGA[A/C]CCCTCAACCTCTTCT | 388795 |
rs553664860 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872169 | GGTGTTGTATAAGGA[G/T]AATAGAATGGGGTTA | 388795 |
rs553688563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896332 | GCCAGTGAGGGTTTG[A/G]GTGGAAAAGCCTTTT | 388795 |
rs553724343 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878619 | GCTTCCCGGGTTCAC[A/G]CCATTCTCCTGCCGA | 388795 |
rs553790175 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870414 | ATACTTTTTTGATAT[A/G]CAGAGAAAATGTTTT | 388795 |
rs553795268 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860031 | TTATTTTGGCCAGGC[A/G]CGGTGACTCACGCCT | 388795 |
rs553797609 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896766 | TCCTGGCCGACACCG[C/T]CTCGCTCCTGGATGG | 388795 |
rs553809259 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859509 | TTTTTCCCATTTGGC[A/G]TTTTACCTCTGTTCA | 388795 |
rs553903205 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910831 | CAGTCTCTGCCTTCC[A/G]GGTTCAAGCGATTCT | 388795 |
rs553937125 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864487 | CTCCAGAGGCTGAGG[G/T]GGGGGGATTGCTTGA | 388795 |
rs553971697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871467 | TTATTTTCTGTAGAG[A/G]TGGTGTCTTGCTATG | 388795 |
rs553975426 | in-del | -/AAAAC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876973 | CCATGTCTCAGGAAA[-/AAAAC]AAAACAAAACAAAAC | 388795 |
rs553990568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951416 | GTGAGAGAAGCCAGA[C/T]GAAAACCTGTACATA | 388795 |
rs554000737 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872660 | TTAGCTGGGCATGGT[C/G]GTGGGTGCCTGTAGT | 388795 |
rs554003596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959244 | GTGATAAGTAATGAG[A/G]GTATTAGGAACAGGG | 388795 |
rs554039528 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866946 | TTTTTTTTTTGAAGT[C/G]TTGCTCTGTTGCCCA | 388795 |
rs554070545 | snp | C/T | 0.000164731 | 0.00907405 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32959803 | GATCTGGCTGAGGCC[C/T]TGATATACCAGCGGC | 388795 |
rs554125277 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928049 | TTTATGATTTTGACT[A/G]TTCTACCTCATGCAA | 388795 |
rs554156750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895665 | CCACCTCTGCCTTTC[A/G]GGTTCAAGTGATTCT | 388795 |
rs554186225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897356 | ACCCTGCGCTTGGTG[A/G]GCTCCCAATACATTT | 388795 |
rs554190811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878063 | TTGAGCCCAGGAGTT[C/T]GAGACCAGCCTGGGC | 388795 |
rs554191893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900971 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCATGAG | 388795 |
rs554208421 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892804 | AGCTGTTGGGGGGCC[A/G]GGGAGGGAGTGGAGG | 388795 |
rs554215633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934945 | ACATTCCCTCCAACA[C/T]TGTACAAGGGTTTTC | 388795 |
rs554251842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890532 | TGCTCAACTCAGTGT[C/T]TCAGTGCCTGGTACC | 388795 |
rs554334683 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886430 | GCACTGCTCTCCAGG[C/G]CTCTACAGAAAGGTT | 388795 |
rs554350759 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928203 | TTTCCTTTTCAGATT[A/G]TTCAACGTTAGTGTA | 388795 |
rs554405060 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879256 | GCAACAGGAAGGGAA[C/G/T]TGCTCCTCAAGCCCC | 388795 |
rs554472763 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895104 | CCAGCATTTGTGACC[A/G]CCTCCTTAAACTGCT | 388795 |
rs554521448 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863551 | AGGACAACTCCTCTC[C/T]ATCAGGGGAAGAAAG | 388795 |
rs554529430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878696 | CCTTGTGCTTTCTTT[C/T]GAGGCAGCAAAAGTA | 388795 |
rs554550740 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934040 | TTTTGTAGAGATGAG[G/T]TCTATGTTGCCCAGG | 388795 |
rs554731922 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859275 | GCCCTGCCCCTCTTC[C/T]GTCAGCTCCGGACAG | 388795 |
rs554830311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902926 | GGACTGACCCCCGGC[A/G]TCTCCCCGACTGTCC | 388795 |
rs554883348 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861264 | AAATTACTACCCACC[A/G]TCCTACCCACTCCAC | 388795 |
rs554937696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885816 | AGCCACACATTTCCC[C/T]TCTGCTAAGCAGGAT | 388795 |
rs554940318 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958632 | TCCTGGGAAGCCTCT[A/G]CCTGGGTTGGGTAGA | 388795 |
rs554965502 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921230 | AGACAGGGTCTCACT[A/G]TCACCCAGGCTAGAG | 388795 |
rs554972612 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957811 | GCTCCCACTCCCAGC[A/T]CTTCTTGGAAAGACT | 388795 |
rs554986845 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874362 | CGACCAGCTGGGACT[A/G]CAGGCTCACGCCACT | 388795 |
rs555005298 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950516 | GTTAGAGCCACACTC[A/T]CTTACAGACTAAGAG | 388795 |
rs555018324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913714 | CCTGTGATGCTAACA[C/T]GTTATGTACTTCCAA | 388795 |
rs555050892 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896089 | TTACTTTTCAGAACA[A/G]AAAGAGCCTAGAGTC | 388795 |
rs555072930 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914768 | CAGGTCCCTCCCTCA[A/T]CATATGGGGATTACA | 388795 |
rs555089349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915320 | CATAGAAATTTGCTC[A/G]GTCAAATATCCAATT | 388795 |
rs555131922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934954 | CCAACATTGTACAAG[A/G]GTTTTCTTTTTTCTG | 388795 |
rs555145202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925367 | TGGGATTACAGGTGT[A/G]TGCCACCACACCTGG | 388795 |
rs555147324 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873213 | GGAACTGGGCAATGG[C/T]GGGGGTGGCCTCCTT | 388795 |
rs555161669 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905035 | CTTAGGCCTGTGAGG[G/T]CTGCAGGGCCCTGGC | 388795 |
rs555234947 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920314 | CTGGGCTCGGGGCCC[A/G]GCCTGATTCTCCCCA | 388795 |
rs555240852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895732 | ACACACCACCATGCC[C/T]GGCTAATTTTTGTAT | 388795 |
rs555268114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919925 | TTAAAGTGGAGGTTT[C/T]CGGGATCCACTGAGC | 388795 |
rs555274102 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877034 | AAACTGAGGCATGGG[A/G]AAGTTAGGAGTTTGC | 388795 |
rs555282569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933925 | GAGGTTGCAGTGAGC[C/T]GAGGTTGCGCCACTG | 388795 |
rs555293676 | snp | A/G | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32906960 | TTGTGGATAGCAGGA[A/G]CAACAGCATCCTCAT | 388795 |
rs555298720 | snp | A/G | 9.22807e-05 | 0.00679204 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889456 | GCCACTGGGAGCCAT[A/G]CATTTGTGCCTGGGA | 388795 |
rs555340378 | snp | A/T | 0.00205934 | 0.0320224 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863758 | CAACGACTGGAGTTA[A/T]GTTGACTATGATTCC | 388795 |
rs555374258 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940084 | CTTCCTTCCTTCCTT[C/G]CTTTTTGGAGATACA | 388795 |
rs555477875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900993 | AGGCATGAGCCACCG[C/T]GCCCGGCCGTCCAGT | 388795 |
rs555478352 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863219 | TTGGTGCTCCAAAGA[A/C]CCTAACAAAACGCTG | 388795 |
rs555543769 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894920 | CACTCTGGCAGTCTT[C/G]GGCAACTTTCCACCC | 388795 |
rs555552102 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869344 | TGGTTCAAGCGATTC[C/T]CCTGTCTCAGCCTCC | 388795 |
rs555624130 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942664 | ATTTTTTGGTGTTCA[A/T]GTCAGTTTTTGTCCC | 388795 |
rs555624218 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913018 | CTGCTCATCCATCCA[C/T]TTATTCATTATTCAT | 388795 |
rs555626537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883031 | AGACGGGATTTCACC[A/G]TATTGGCCAGGCTGA | 388795 |
rs555629430 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941439 | TGAATGTTTATAGTA[A/G]CATTATTTATAATAC | 388795 |
rs555663931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912520 | TCCTATCACTCAGTA[A/G]TGACTTGACCTTAGC | 388795 |
rs555675632 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877276 | TGCAATGGCACGATC[G/T]TGGCTCTTTGCAACC | 388795 |
rs555716692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940677 | TCATATATCTGATAA[A/G]GGACTAGTATCCAGA | 388795 |
rs555794121 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888958 | TTGGTTGGTTTTTTT[G/T]GTGGGGGGCGGGGGG | 388795 |
rs555820047 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918165 | AGCAGTGTCCTGCCT[C/G]TGGGTACTCAGGGCA | 388795 |
rs555833620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894436 | GCTTGAGCCTAGTCA[C/T]TCTGCGCCACCGTGG | 388795 |
rs555884863 | snp | C/T | 9.22297e-05 | 0.00679016 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32911638 | AGGTTTGCGGGATGG[C/T]ACAATGAAGATGTGG | 388795 |
rs555916758 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959102 | GAAAATGTGTATTGA[A/G]ATCCTACTGACTGCC | 388795 |
rs555960388 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | EFCAB8 | GRCh38.p7 | 20:32962167 | TCTGCCGCTGTCAGG[C/T]TATGGAGTCCCATGT | 388795 |
rs556017246 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859386 | TTTTACATCTCAGCC[C/T]TCCCTTCCTTCCCTT | 388795 |
rs556036579 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914644 | TGGTGGCAGGAGAGA[A/G]AGTGCAAGGGAAACT | 388795 |
rs556057375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956886 | TCTCATTGTGGGGGT[A/G]CTAACTATATGTATA | 388795 |
rs556067970 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877951 | CTCTTTCAGTGAATG[C/G]TGCGAGTAGGCCCTT | 388795 |
rs556083287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901147 | TGCTTTGAATGGGGC[C/T]GTGTGGCAGAAGTTT | 388795 |
rs556096547 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927204 | AATTACAAAAGTCAC[C/G]AGAACTTACCAGTTC | 388795 |
rs556115209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884621 | GCCCAGGGTCAGACC[A/G]GGCCTACCGGATTTG | 388795 |
rs556141292 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910443 | CTTCTGAGGTGTGAG[A/G]ATAGGAGGGGCTGCT | 388795 |
rs556153418 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929814 | CAGGCAAGAAACTTT[C/G]TTCTCATGCTTGCCA | 388795 |
rs556172924 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890154 | TGTGGTCTGTGAGGC[C/G]TTCAGAGGTCTGAGC | 388795 |
rs556180877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895024 | GTTTGGCATGAGCCG[C/T]CAGATCCATCCTTGC | 388795 |
rs556204448 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864625 | GTCAAATGCAACACA[C/G]CCGAGCCCCCTGATG | 388795 |
rs556204508 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872054 | TCCAGATAAACAAGA[C/T]GGGTCCCTCTTTTAG | 388795 |
rs556244334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889531 | TGGGAGGATAGCCAG[A/G]TGGAGAGGCCTTAGT | 388795 |
rs556308844 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902872 | CAGGAGCAAATCTGA[C/T]GGAGCGGGTGTGGTA | 388795 |
rs556374493 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913069 | CCTTTTGCTAGGTGC[C/G]TGGGATGGGTATAAA | 388795 |
rs556415048 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922906 | AAAAAAATTCAGGCC[A/G]AGAGCAGTGGCTCAC | 388795 |
rs556426618 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945791 | CTGGGTGCCTCCCCA[A/G]TCTTTTTTGTGGATA | 388795 |
rs556460445 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868479 | AAAATACCCCTAGTC[C/T]AAATACCCACATGTA | 388795 |
rs556460806 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891586 | CTGTCATCTGCTCGG[A/T]GGTACTCAGACAAGG | 388795 |
rs556467035 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871359 | GTTCACTGAAGCCTC[A/G]ACCTCCTGGGCTCAA | 388795 |
rs556467958 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957727 | TGCTGGTTTCTCTCT[C/T]TCTAAGCCAAGTCTG | 388795 |
rs556498892 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933953 | CTGCACTTCAGCCTG[G/T]GCAACAAAGTGAGAC | 388795 |
rs556588938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883835 | AGCTGGGACTACAGG[C/T]GTGTGCTACCACACC | 388795 |
rs556594465 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906757 | TCTCCTGCTGCTCTT[A/G]TCCCCACTTCTGGGC | 388795 |
rs556610432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869324 | CTCACTGCAACCTCC[A/G]CCTCTGGTTCAAGCG | 388795 |
rs556611865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941596 | GAAAATACTGTGCTA[A/G]GTGAAAGAAGCCAAC | 388795 |
rs556621565 | in-del | -/GGAAACCCCT | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920581 | AGAAGCAGCAAAAGC[-/GGAAACCCCT]GATAAACCCATCAGA | 388795 |
rs556666240 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926236 | CTTTGGTGAATCCTG[G/T]GCAGTTATGAGGAAC | 388795 |
rs556673770 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882905 | TTTCACCATGTTAGC[C/T]AGGATAGTCTCAATC | 388795 |
rs556711674 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863233 | ACCCTAACAAAACGC[G/T]GTCATCCATCTCATA | 388795 |
rs556712998 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939525 | CCTGACTTTGTGGTC[C/T]GCCTGCCTTGGCCTC | 388795 |
rs556756246 | in-del | -/CAGGGTTTCAATATGTTGGC | 0.00557542 | 0.0525036 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862817 | TATTTTTAGTAGAGA[-/CAGGGTTTCAATATGTTGGC]CAGGCTGGTCTCATT | 388795 |
rs556781913 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | EFCAB8 | GRCh38.p7 | 20:32962203 | TCCCCTCTGGCCCAG[A/G]GGCACCTTTCCAGAC | 388795 |
rs556787769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948490 | AGGCAACTTGGTACC[A/G]AAATCTGACAAAGAC | 388795 |
rs556871159 | snp | C/T | 0.000805802 | 0.0200562 | missense | EFCAB8 | GRCh38.p7 | 20:32959840 | AGGCGGCGCTGATGG[C/T]TCTCCTGCATGGGAA | 388795 |
rs556908262 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931910 | AAATGGAGAACTCTT[C/T]AAACAATTTAGGCAA | 388795 |
rs556928031 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924551 | GAAGAAACAGGCCCA[A/T]TGAGGTGAAGTGACT | 388795 |
rs556946287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882356 | TTGGTCACTTGATAG[C/T]TGTTCACGGCACACT | 388795 |
rs556986637 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946408 | GTTTTTTGTTTTTTG[G/T]TTTTTTGGTTTTTGT | 388795 |
rs557025470 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903785 | GAGGCTGATACGGCA[A/C]AGTCAGGGGCCTGGG | 388795 |
rs557054078 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886714 | GCTTGTGGCTGCTAC[A/G]TGGTCACCAAAGCAC | 388795 |
rs557086808 | snp | C/T | 8.79624e-05 | 0.00663125 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32961186 | TGATCTGATGCCGAC[C/T]CAGCAGCCTGACTTC | 388795 |
rs557091438 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912389 | GTGAGCCGAGATCCC[A/G]CCATCGCACTCCAGC | 388795 |
rs557095318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923378 | GTAGTCCCAGCTAGT[C/T]GGGAGGCAGAGGCAG | 388795 |
rs557098103 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861017 | GTTGGCATTACAGGT[A/G]TGAGCCACTGTGCCT | 388795 |
rs557102295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954113 | ACCCAGCATGATTAC[A/G]TTTTTTGATACACAG | 388795 |
rs557144392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922722 | AGGAAACATGGCCTG[C/T]AGTTATTTGGAAGGA | 388795 |
rs557219977 | snp | A/G | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32917435 | ACATCCTCTTCTGGA[A/G]CACCGGCACACTCAA | 388795 |
rs557236548 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898949 | GAAAGCACGTACCTC[A/C]CTTCCTGAAGGGTTG | 388795 |
rs557258545 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917032 | TTAAACCTTAATCCT[G/T]ACCTAGGTGTCTGAC | 388795 |
rs557260496 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932411 | TACTACACTTATATA[C/T]GATTTTCTATGTGTA | 388795 |
rs557286940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955191 | TTATCCTAGCTGGCC[A/G]TTAGAGACAAGAACA | 388795 |
rs557312763 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954908 | TCAAGATGTATTATT[A/C]TTTTAATATATTGTT | 388795 |
rs557326074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957221 | AATCTGCTAACTCCA[A/G]TGTGAATCTTCTGGA | 388795 |
rs557339857 | snp | G/T | 8.79624e-05 | 0.00663125 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32961162 | GGTCTACCAAAGCCT[G/T]CACTTCAGTGATCTG | 388795 |
rs557360303 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910306 | CTTGGGCATCTCTTT[G/T]CAGGGAAGCCATAAC | 388795 |
rs557389964 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868362 | GCCACTGTGCCCAAC[C/G]CTGATCAGCATCTTT | 388795 |
rs557437749 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919798 | ACCACCACGACCGAC[A/C]TTTATCCTCATTTTT | 388795 |
rs557442295 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904399 | TCAACCTCCTGGGTT[C/G]TAGCAATCCTCCCAC | 388795 |
rs557447881 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877247 | GGAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG | 388795 |
rs557466505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861837 | CCAGAGATGACTGCT[A/G]TTAATTTTGGAGTAT | 388795 |
rs557537543 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870781 | TGTTGGGATTACAAG[C/T]GTTAGCCACTGCACC | 388795 |
rs557543167 | snp | A/G | 0.000399281 | 0.0141238 | stop-gained | EFCAB8 | GRCh38.p7 | 20:32930580 | TGATAAAAATGACTG[A/G]ATCCTCATCACGGGG | 388795 |
rs557558342 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887035 | GGAGAGAGGGGCTTA[C/G]GAGGGTTCTGGTCCA | 388795 |
rs557660887 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874335 | TCAAGCCATCCTCCC[A/T]CCTCAGTCTCTCGAC | 388795 |
rs557664630 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889910 | AGGAGGCTGAGGCAG[G/T]AGAATCGCTTGAACC | 388795 |
rs557677354 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903543 | TTTGTTGATCAATAC[A/G]TGAAATCGGCCTGAA | 388795 |
rs557687744 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904906 | TGCTGGGATTACAGG[C/T]GTGAGCTACTGTGCC | 388795 |
rs557726791 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874770 | TCCTTTCTTTCTGAC[A/G]GAGTCTGGCTCTGTT | 388795 |
rs557737428 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876619 | TGTGCTAAGCTCTCT[A/G]TGTATTATTTTACTT | 388795 |
rs557741660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919237 | AGTGAGATTGTTCTC[A/G]TAGTCAAAATCTGAT | 388795 |
rs557839258 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907503 | CTCTGCAGCTGTAGG[C/T]TCAGGATACTGCCCC | 388795 |
rs557887448 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946505 | CAGTGTCTCCATAGG[A/G]AGAAGGAAGTTCTGG | 388795 |
rs557920505 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906005 | TGACTTTTCCTTTTG[G/T]TGTCTCTATCCCTAG | 388795 |
rs558023798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904456 | CAGGTGCACCATCAC[A/G]CCCAGCTAATTTTTG | 388795 |
rs558029462 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888272 | GCTCTGTCACCCGGG[C/G]TGGAGTGCAGTGGTG | 388795 |
rs558050279 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935420 | GGTCAGGCTGGTCCC[A/G]AACTCCTGACCTCAA | 388795 |
rs558062604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911097 | TGTTTCATTGAGTGG[C/T]ATGGCTGTCCTTATT | 388795 |
rs558077504 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917142 | TAGTAAGCGCTTAGT[A/T]AATGAGGTCAATGGG | 388795 |
rs558080226 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938873 | TAATGCAATTTATAT[A/C]AAAATCCCAGCTGCT | 388795 |
rs558092528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888877 | CCCTTTGAGTAGGTG[C/T]AAACACACCCATAGA | 388795 |
rs558092765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882414 | ACCTCACACAGTTCC[A/G]GAATCAGTCCTGGGG | 388795 |
rs558124536 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909541 | CTGATTGAGGCTTCA[A/G]CTTCTCAGAAGTTAT | 388795 |
rs558126559 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955110 | ATTTTTCTGGTAAGT[A/G]GAGATAGAGCTGTAT | 388795 |
rs558188583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869160 | TACAGTTCCTGGCCA[C/T]GCAGGATTCACCAAC | 388795 |
rs558199443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887458 | GCGCACCCCTGTAAT[C/T]CCAGCTACTTGGGAG | 388795 |
rs558214775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893870 | TCAGGAGGGAGGAGC[C/T]GCTGCTGCAGCCCAT | 388795 |
rs558238141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887069 | TCTTCACCGCCAGAA[C/T]CACCTGGGGAGCCCG | 388795 |
rs558312700 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875146 | TTAGTGCCTCCCCTC[C/T]CCACACTGCTGTGGG | 388795 |
rs558338661 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866848 | CTTCCTTCCTTCCTT[C/T]CTTTCTCTCTCTCTT | 388795 |
rs558339161 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880566 | GTGAGCCACTGTACC[C/T]GGCAATAACTTAAAA | 388795 |
rs558354718 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864326 | TGGTGGCTCACACCT[-/G]TAGTCCCAGCACTTT | 388795 |
rs558362490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881447 | AGTGATCCATCCACT[C/T]CGGCCTCCCAAAGTG | 388795 |
rs558363894 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863388 | AGTGGAAATGAGGAG[C/G]CCTCATTTTTCTAAT | 388795 |
rs558380585 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32961534 | GCACATTGTCTCCTC[C/T]TTCGAGCGGCCCCCA | 388795 |
rs558414068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892097 | GTGGTTGCCATGGGG[A/G]AAAAAGGGCTGAAGG | 388795 |
rs558414919 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923423 | CCCGGGAGGCGGAGG[A/T]TGCAGTGAGCTGAGA | 388795 |
rs558424376 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903074 | ACCCACGGCCATCAA[C/T]AAATCTGATCCAGCC | 388795 |
rs558444980 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907411 | CTAGTGACCCCTCCT[C/T]GGCTGCCTGGCCATG | 388795 |
rs558446038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881428 | TCTCGAACTCCTGAC[C/T]TCAAGTGATCCATCC | 388795 |
rs558456538 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861104 | AAGTCAGATTCATCC[A/T]TCTGATGTTTGGGTG | 388795 |
rs558457538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868434 | TATTGCAAGCATATT[A/G]GAGGCTATTTGGGAT | 388795 |
rs558467494 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860706 | AAAAATTGGCATCAT[A/T]GTGTGCACCCTTTTC | 388795 |
rs558566119 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930744 | TTTGTGAAACAATGC[A/T]GCGAGGAGTCCTCTC | 388795 |
rs558591886 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960668 | GATCCCAGCCTCCCC[C/G]TCCTTGTCTGCCAGG | 388795 |
rs558597078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897370 | GGGCTCCCAATACAT[C/T]TGCTGCACAAATGAA | 388795 |
rs558597861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866128 | GCAGGGACCCTCACT[A/G]TGTTCACGGTGTATC | 388795 |
rs558603823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937917 | CCACCACACCTGGCT[A/G]AAGAATTAATGTCAA | 388795 |
rs558705381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936182 | GGATTATAGGCGTGT[A/G]CCACCATGCCTAGCT | 388795 |
rs558725309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879493 | CATTGGCAGGGACCT[C/T]TCTAAGCGAAGACAG | 388795 |
rs558726586 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931393 | AGCCCCACAAATGAG[C/G]TAGGACCATAAACTA | 388795 |
rs558742189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935567 | ACTGGAGTGCAATGG[C/T]GCAATTGCAGCTCAC | 388795 |
rs558743995 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944031 | TATATTTTTGCAAAT[C/G]ATATATCTGATAAAG | 388795 |
rs558750203 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863961 | ATACTCAGATATTTA[C/T]TGGGCAGGTAACTTA | 388795 |
rs558797842 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897834 | GTGTAAAACCCAGCT[C/G]AGGGTCTTGCATGTA | 388795 |
rs558846600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937163 | TTTTGTATTTTTAGT[A/G]GAGACAGGGTTTCTC | 388795 |
rs558873112 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895528 | TTTTTGTAGAGATGG[A/G]TTCTCACTGTGTTGT | 388795 |
rs558892640 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879802 | GGTCAGACAGTCCTT[A/C]CTGAACATACTGCTT | 388795 |
rs558913991 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869239 | AGATGGGTGTTGCAA[-/T]TTTTTTTTTTTTTTT | 388795 |
rs558948700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880774 | CCGTGTGTTCAGCCA[C/T]AGGGAAGCTCTCAGA | 388795 |
rs558980656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873399 | GCACTTTTTAAAGAT[C/T]GTGATTATTAAAAAA | 388795 |
rs559011707 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32959844 | GGCGCTGATGGCTCT[C/T]CTGCATGGGAAGGCA | 388795 |
rs559012243 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903979 | ACTGTGTCAGGGGGT[C/T]GGGTGCCCTACTACA | 388795 |
rs559050734 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910021 | GTGCCTGGGTCTGTA[G/T]TCAGCTCCCATGGCA | 388795 |
rs559089420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916482 | CAAGCTGGTCTTGAA[C/T]TCCTGGCCTCAAACG | 388795 |
rs559093377 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909706 | CTGGAATCAGGCCTG[A/C]GTGTGGTCAGGACGT | 388795 |
rs559116017 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874702 | ACACGCCACCAAACA[C/T]GGCTAATTTTTGTTT | 388795 |
rs559133599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873827 | AAAAAAAAAAAAATG[C/T]AGTTCACCTCTCCTT | 388795 |
rs559160750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886204 | ATGGGGCTAGTTACA[A/G]TGCTTCTTTACAGTC | 388795 |
rs559162170 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951509 | AGGAAATGCAAACAA[A/G]TGTGTAGTGTGACAG | 388795 |
rs559175666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911206 | AGTAATGTCTTTTCC[A/G]TATAGGGATTATTTT | 388795 |
rs559188129 | snp | C/G | | | utr-variant-3-prime | EFCAB8 | GRCh38.p7 | 20:32961677 | GTCCTGCATGTTCTC[C/G]GCTTATTCCCTACCA | 388795 |
rs559198090 | snp | A/C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879714 | ATAGCAAGGACGTTA[A/C/G]TTCAGATTCTTGTCC | 388795 |
rs559209346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885394 | CGTGCGTGTGCGTGA[C/T]GCTCCGCCGGCTTTT | 388795 |
rs559239444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890796 | GCTTTACCTCCCAGT[A/G]CCTCGCTTTACCCAG | 388795 |
rs559266345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917207 | ATCCTCCTCTGAGTC[A/G]GCTCCCAGAATCCTC | 388795 |
rs559288455 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949008 | AGAAGGAAAAAAAAA[-/G]GGCATTCAGATTGGA | 388795 |
rs559299538 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860185 | TGGTGGCGTGCACCT[A/C]TAATCCCAGCTACTG | 388795 |
rs559349215 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887127 | CTCTCTGAGTTCTGA[G/T]GGAACAGGCTCCTCT | 388795 |
rs559393266 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923537 | GAAACTTTATACGAG[A/T]GTATAAAGTAAAAGA | 388795 |
rs559402066 | snp | A/G | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32961301 | GAGCAGGCTGTGCTG[A/G]ATACCACGGACAGCA | 388795 |
rs559432083 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960857 | AGGGTCCAGCTCGAG[A/G]CCTCATTCTCAGAAG | 388795 |
rs559484763 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944334 | GCCAGGCATGGTGGT[A/G]CATGCCTGTAATCCC | 388795 |
rs559536926 | snp | A/G | 9.35848e-05 | 0.00683986 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892324 | CTGGGTGTTCCTCAC[A/G]TGAACCAGGAGGCCC | 388795 |
rs559550532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936441 | CTAGTTGTTTTACAG[C/T]CTCAGATCTTATATT | 388795 |
rs559571403 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891390 | ACCCAGCAAATTTTT[A/G]TATTTTTAGTAGAGA | 388795 |
rs559588097 | snp | A/G | 0.00010548 | 0.00726145 | stop-gained | EFCAB8 | GRCh38.p7 | 20:32959880 | GGAGGCAGACACTTG[A/G]GCCAAGCTGCAGAAG | 388795 |
rs559589963 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951826 | TTCAGATCTTTTGCC[A/G]TTAAAAAAAACTGTG | 388795 |
rs559605721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897169 | CCCAAGCAGCCCTCC[C/T]AGGACAACCCTGTGC | 388795 |
rs559658119 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915075 | GCTAATTAAAAAAAA[A/T]ATTTTTTTATAGAGA | 388795 |
rs559697297 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927610 | TTGGCTTCCCAAAAT[G/T]CTGGGATTAGAGGCG | 388795 |
rs559701856 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935615 | AGGTTCAAGCAATTC[A/T]CCTGCCTCAGCCTCC | 388795 |
rs559723198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923150 | GATTGTGCCACTGCA[C/T]TCCAGCCTGGGCAAC | 388795 |
rs559723749 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901024 | GCCTTTTTAACCAAA[C/G]AGTGCACTGTGTACA | 388795 |
rs559736430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902660 | TGCAATGTACAGGCC[A/G]GCAGGTGGCACAATT | 388795 |
rs559738208 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866255 | TTAGTTGGGGCTAAG[A/T]GGGGGAGAGTGAGCA | 388795 |
rs559760982 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944905 | ATAAGCTTTTTGTCC[C/G]TTTCTCTCTCTCTGT | 388795 |
rs559825108 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943342 | GCACTTGGTAAACAA[C/T]GTAGTCATATGCAAG | 388795 |
rs559855844 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928456 | TGACCAGGCTGGTCT[C/T]GAACTCTTGACCTCA | 388795 |
rs559867813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900734 | ACCATGCCCGGTTAA[C/T]TTTTTTTCATATTTT | 388795 |
rs559869796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907750 | GACAGGGACAGTCTC[A/G]CTGAGGTCCCCAGTC | 388795 |
rs559901423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903189 | TCTCCTCCTGGCCCA[C/T]CTGGTGCCCACCACA | 388795 |
rs559931723 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890176 | GGTCTGAGCCCTGCC[A/G]CCTCCAGTAGTCTCC | 388795 |
rs560025384 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915582 | GTCCTCTTTTCTTTC[G/T]AGGCCCTCACTGGAA | 388795 |
rs560031843 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901209 | GCATTGGTGGTGGTA[A/T]CACTTAGTGTATATT | 388795 |
rs560076498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901993 | TCCTGGCCTTGTTTT[C/T]TAAATTAATTAATTT | 388795 |
rs560080628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909130 | AGGCCTCCCACGCTC[C/T]GTGGGCTGGGCCACC | 388795 |
rs560088305 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950823 | CTGTCCTATTGTATT[C/T]TACTGTCTGCTCTTT | 388795 |
rs560119918 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908602 | GTTTCTAGGCCCCCA[G/T]CCTGTCACCCTCTCT | 388795 |
rs560153572 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865286 | GTAGGGGTTCACCTC[C/T]AGGGGAGATGGGTTG | 388795 |
rs560162251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883925 | TGAACTCCTGACCTC[A/G]AGTGGTCTGCCCGCC | 388795 |
rs560205173 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907121 | GGAGGGGCCCCGGGT[A/G]GGAGGAAGGTGAGGG | 388795 |
rs560251744 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878476 | GGGAGAGATGGGGTG[C/G]TGAGGGGGACCCTGG | 388795 |
rs560274672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888567 | CCCTATGTTGCCCAG[A/G]CTGGTCTCGAACTCC | 388795 |
rs560276343 | snp | C/T | 0.000376152 | 0.0137089 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885482 | TTTGCTTGGGCTCTT[C/T]TCTCTTTCATCGCCT | 388795 |
rs560292114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942203 | GTCCTAAGTGAGCAA[A/G]ACATTTTTGGTTGAT | 388795 |
rs560337846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870998 | CGAGTAGCTGGGACT[A/G]CAGGCACGCACCACT | 388795 |
rs560366023 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864671 | GACTCCACTTCTCTA[C/G]TTAATTTTGTCCAGC | 388795 |
rs560411437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913343 | AGGGTTAAGAAATCT[C/T]TCTGGGGCCTCCTTT | 388795 |
rs560412119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895266 | CATGAGGGCTGCACC[C/T]GGCTTGCCTGAATTC | 388795 |
rs560425571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958829 | GATGGGGCCCTGTCC[C/T]CCAGCCAGGCCCAGA | 388795 |
rs560427222 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864254 | TGCTGGGACTACAGG[A/C]GTGAGCCACCACACC | 388795 |
rs560491594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926344 | ATGACTACTGTGAAA[A/G]TTGTGTGCACGTTAA | 388795 |
rs560507457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912684 | CCTGTAGGTGATTTT[C/T]GTCATCCAGAGATTT | 388795 |
rs560533464 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921574 | TAATAATACTAGTTT[A/G]TAATAAAAAAGGAAG | 388795 |
rs560541981 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940827 | AATGATGGTGAACAT[C/G]ATTAGCTATCAGGGA | 388795 |
rs560542486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919575 | GGTCTTCGCTCAGTG[C/T]AACCTCTGTCTCCTG | 388795 |
rs560646921 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897080 | CCGCCTCTGTGCCTC[A/G]GCATGTGCTGCGCCT | 388795 |
rs560652402 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933633 | TCCCTTATTCCCCAC[A/C]CCACCCTCTAAGCCT | 388795 |
rs560702106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895863 | GGCGTGAGCCACCGT[A/G]CCTGGCCCAGGCTGG | 388795 |
rs560703964 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901933 | CCTCATGATTCGCCC[G/T]CCTCGGCCTCCCAAA | 388795 |
rs560757638 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920945 | AACACGAGTTGGGTA[A/T]GGGTTCATCTTTGTT | 388795 |
rs560763719 | snp | A/G | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32885585 | TCCTGACTGTCACCA[A/G]AGACGGGATCCTGCA | 388795 |
rs560808671 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925708 | CCCCAGTAGGGAAGG[A/G]CCAGATGGCACGCAG | 388795 |
rs560819679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873272 | GAAGGAGCCCCCTGA[A/G]CTCTGAGGATGTTGG | 388795 |
rs560855086 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882970 | AAAGTGCTGGGATTA[C/T]AAGCGTAAGCCACCG | 388795 |
rs560893876 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941036 | AGGTGGGCGGATTAT[G/T]AGGTCAGGAGTTTGA | 388795 |
rs560953237 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936276 | TGACCTCAGGCAATC[C/T]GCCTGACTCAGCCTC | 388795 |
rs560973643 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875416 | AGCCATCTCCCTTCT[C/G]TGCCCCCTGCAGTGG | 388795 |
rs560985565 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878966 | CTCATTTCAACCTCA[C/T]AGCCCTGTAAGTGTT | 388795 |
rs561043104 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886028 | CCACGTCCTACCGAT[G/T]CAGGCCTTTTGCCTA | 388795 |
rs561091550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914241 | TGAAGTTAAGCGATG[A/G]TGGTAGAGTGCTGTG | 388795 |
rs561092573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951561 | ATAGGGGGCTGATGA[A/G]GGTTGGAAGGGTGGG | 388795 |
rs561135692 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859579 | TTATCTTACAAAATA[C/T]TTAGTTTTGAAATAA | 388795 |
rs561148205 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865390 | TGTGCCTGGAACATG[C/G]TGCATGCTTGAAACT | 388795 |
rs561268870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920444 | AGCTGATAAAGGCAT[A/G]TCCGAGACTGAGAAG | 388795 |
rs561337496 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949922 | CAAGAATCGCTTGAA[A/C]CTGGGAGGCGGAGGC | 388795 |
rs561397801 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959322 | GCTTCGTAGGAGAGG[A/T]GATTTTGGAGTTGGG | 388795 |
rs561424262 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32908361 | AAACTGCCCCATCAC[C/T]AGTGCCTACTTCTTC | 388795 |
rs561443096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926490 | TTTCCTCTCAGCACA[C/T]AATAATCTATCCACT | 388795 |
rs561546352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918625 | CTCTCTAGCCGCCGG[C/T]GTTCACACACCGTCT | 388795 |
rs561592958 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884686 | GTTCTAGTTCCAGCC[C/G]TGCTAGTAAATAGGA | 388795 |
rs561605868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927406 | CTGGAGTGCAGTGAC[A/G]TGATCTTGGTTCACT | 388795 |
rs561632291 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911268 | GAGTTAACAGGTCTT[A/C]ACCAAACGTTCCAGT | 388795 |
rs561712359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941008 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCTGAGG | 388795 |
rs561744033 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936885 | TGCATTGAATCTGTA[A/G]ATTGCTTTGGGTAGT | 388795 |
rs561770832 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869280 | TTCACTCTTGTTGCC[C/T]AGGCTGGAGTGCAAT | 388795 |
rs561784535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894662 | CTGTGTGACCTGGAG[C/T]CAGTTGCTTAACCTT | 388795 |
rs561801900 | snp | C/G | 0.000837716 | 0.0204489 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889296 | TCTGCTCTTCCTCTG[C/G]CCAGCTTAACCAGAC | 388795 |
rs561823843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906324 | GCCTGTGGGCTGTTG[A/G]TTTGGGGCCAGGACT | 388795 |
rs561846102 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907732 | CTGAGTCTGGGGCAT[A/G]GGGACAGGGACAGTC | 388795 |
rs561884766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912022 | AATTCACAGCCACCC[A/G]TGGTCACCCCTATTT | 388795 |
rs561885327 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924698 | GGCTTTTTACGTGGC[C/T]TGGTGATCTGTGTGT | 388795 |
rs561897481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898062 | TTCTCATGCCCTCCG[C/T]GCTTCCTTGAGCACT | 388795 |
rs561900393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892918 | CCATCTTAGCTCACT[A/G]CAGCCTCCACCTGCC | 388795 |
rs561901853 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904473 | CCAGCTAATTTTTGT[G/T]TTTTTTGTACAGATG | 388795 |
rs561964145 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914347 | AGGGACAGTCCTGAT[-/G]GATCTCTGAGTTGCC | 388795 |
rs561964989 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939850 | CAGGTGCCCGCCACC[A/G]TGCCTGGCTAATTTT | 388795 |
rs561977018 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893961 | AGATCTGAAGTCCGG[A/C]TGCCTGCCCTGGAGT | 388795 |
rs561979907 | in-del | -/AG | 0.00358779 | 0.0422022 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863555 | CAACTCCTCTCTATC[-/AG]GGGAAGAAAGGCTCA | 388795 |
rs561988744 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905382 | TGATGAAGAATGGAC[A/G]GTCATGCAGGACGAC | 388795 |
rs562057337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898657 | CTGGCTAAGGCGGTG[A/G]GGCTGGAAGGGAGGG | 388795 |
rs562135140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942807 | TCTAGTATTCATTTG[A/G]GTGTAAGATAAAAGA | 388795 |
rs562137063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934501 | ATTGCTAGATCATAT[A/G]GTAGTTCTAATTTTA | 388795 |
rs562142638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938394 | CCTGTAAAATCAGAA[A/G]TAAAACAAGAATGGT | 388795 |
rs562153520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887953 | TATGGAGGGGCAGAC[A/G]GGGGAAGTCAGTCTT | 388795 |
rs562179815 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945929 | GCAAGTTCTCTAGAG[C/T]GGCTACAAGCTTCCC | 388795 |
rs562183577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868581 | TGATAATACCACAGT[C/T]TTAGTGGCTTAAACC | 388795 |
rs562198929 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935021 | ACATCTAATCTAACA[G/T]ATGTAAGATGATATC | 388795 |
rs562211012 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882694 | CCTGGCCGATTTTTT[G/T]TTGTTGTTGTTGTTG | 388795 |
rs562238789 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903449 | TCCTGTTGTTTCCCT[C/G]TAGAAGGAAAACCCC | 388795 |
rs562242992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862056 | TGTGTGTTTCTCCCT[C/T]TTTCTGTCCTCTAAA | 388795 |
rs562436931 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914620 | AGGGGAAGCAAGGCA[C/T]ATCTTACATGGTGGC | 388795 |
rs562450932 | in-del | -/CC/CT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939203 | TTCTTTCTTTCTTTC[-/CC/CT]CTCTCTCTCTCTCTC | 388795 |
rs562472731 | snp | A/T | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859232 | GAATTCTCACCCCTG[A/T]TCTGGATGGTACTCT | 388795 |
rs562526348 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918709 | TCAACTCACTTGTTT[G/T]GAGCATTGTGGGCCT | 388795 |
rs562552569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890093 | GCCCTCTGCAGAAAG[C/T]CTTCACCCTACCCCA | 388795 |
rs562561788 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926691 | ACAGTCCCCAGAGTG[C/T]GATGTTCCCCTTCCT | 388795 |
rs562576660 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864555 | CCATTGCACTTATCC[G/T]GGGCAACAGAGCGAG | 388795 |
rs562586646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884151 | TTCAACCTACAAACC[C/T]GGAGAGCATTTCCAA | 388795 |
rs562592221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889685 | TGCCACTCCTAGTCC[A/G]GGCCCCCTTCACTGT | 388795 |
rs562593849 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895764 | TTTGTAAAGACAGGG[A/T]TTCACTATGCTGGCC | 388795 |
rs562656809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863528 | TTGTGAAACCCCATG[A/G]CTTCTGCAGGACAAC | 388795 |
rs562677890 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906362 | TGCTTTGCCTGTGGT[G/T]CTGAGCCCTGACTTG | 388795 |
rs562702687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893662 | GCTAACTAACTTCCT[C/T]GGATGGTGGCGAGGA | 388795 |
rs562704133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872771 | CACACTCCAGCCTGG[A/G]CAACAGAGCGAGACT | 388795 |
rs562718171 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870302 | ACTGACCTTGGCCAT[A/C]GTTTTTATTGTGTTT | 388795 |
rs562743042 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864015 | AGAGTCTCGCTCTGT[A/C]GCCCAGGCTGGAGTG | 388795 |
rs562743413 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957392 | TTGATATTATTTCCC[A/C]CAGAGCATTTGCTCT | 388795 |
rs562755638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933556 | GCAGAAGATCTCAAA[A/G]CTTTTTCCTCCTGTC | 388795 |
rs562815489 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891012 | TGTGACCCGCCTGGG[C/T]TTTCCACTGCAACAT | 388795 |
rs562825048 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888387 | AGCACCACCACGCCC[A/G]GCTAACTTTTGTATT | 388795 |
rs562832312 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900108 | GATTTAAGGCCTGTA[C/T]TGGGGAGAGACTGGG | 388795 |
rs562899302 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899114 | TTAGTCACCGGGCGC[C/G]GTGGCTCACGCCAGT | 388795 |
rs562922328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924781 | TGCAAAAGATTGAAT[A/G]TCTATTGGTGAGATT | 388795 |
rs562944838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882679 | GTGGCCGCCACCACG[C/T]CTGGCCGATTTTTTG | 388795 |
rs562990635 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875266 | GTGAGGACAGAAGCG[G/T]CCGGAATTGGCCTAG | 388795 |
rs562993249 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862020 | AGGTCACTTTGTAGC[A/G]TCCCATTCTCCTAGC | 388795 |
rs563003639 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910023 | GCCTGGGTCTGTAGT[C/T]AGCTCCCATGGCACA | 388795 |
rs563027004 | snp | A/T | | | missense | EFCAB8 | GRCh38.p7 | 20:32911603 | ATGGCCCTGGATGAG[A/T]CAGAGCGGTGCCTGC | 388795 |
rs563027465 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867160 | CCTGACCTCAAATGA[C/T]CCGCCCTCCTCGGCC | 388795 |
rs563039388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898760 | TCCAGCATTGCCAGC[A/G]GCAGCACGGTGAGAA | 388795 |
rs563104847 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939288 | TCTCCTTTTTTTTTT[A/T]GTTTTTTGTTTTTTG | 388795 |
rs563107081 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885057 | CGGTTCTGTTCCCCC[C/G]TCTACCCCAGAGCAC | 388795 |
rs563200468 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874969 | GGTCAGGCTGGTCTC[A/G]AACTCCTAGCCTCAG | 388795 |
rs563205796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955817 | AAGGGAGGGAAAAAG[C/T]TGTTTCTCTATTTTT | 388795 |
rs563234857 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905107 | CTCACCCGGCCCTAA[A/T]GAGCCTCTCCTCTCC | 388795 |
rs563247011 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911385 | CGTCTGTTTTCTCAG[G/T]GGATGGAGGGGAGGG | 388795 |
rs563262037 | in-del | -/A | 0.284995 | 0.247539 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860313 | CTCAAAAATAAAAGC[-/A]AAAAAAAAACCCAGT | 388795 |
rs563264906 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946266 | TGCATGTTGGATGTA[C/T]ATCTCAGTCTTTCCC | 388795 |
rs563368714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944979 | CATTTGACGATGTCT[C/T]ATAAATCCCTTAAGT | 388795 |
rs563403533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881755 | GAGAATAGGGTTACA[C/T]GAGTTCCAAACTCGC | 388795 |
rs563458774 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923599 | AATTACGTTAAGACA[G/T]GTGTTGTAGCCTTCT | 388795 |
rs563501428 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928736 | CTCTGGCAGAACTTC[C/T]AGTACTCTGTTGAAT | 388795 |
rs563512482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930858 | CATCACTGTCTTCTC[C/T]AACTCCCTCATCCCG | 388795 |
rs563513033 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916288 | TAAGAGACAGGATCT[A/T]GCTCTATTGCCTAGG | 388795 |
rs563584662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930230 | CATAGTCGAGTATGA[C/T]GTTCCTTGTCACCAG | 388795 |
rs563612777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886639 | CTGTGGCTTCCATAG[C/T]CATCCACCTTACCTT | 388795 |
rs563643007 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931961 | ACATATATTAGAAAT[A/G]ATTGTTTTTGTTGGG | 388795 |
rs563712850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866271 | GGGGGAGAGTGAGCA[A/G]TTTAATCCCTTGTCT | 388795 |
rs563767844 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32960083 | CAAAGTCTTGGGAGC[A/G]GCGTATAAGCCCAAG | 388795 |
rs563771006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955994 | TATGTAGTTGGGTTG[A/G]AGTCAATCATCTTGC | 388795 |
rs563776689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862300 | CACACCTGGCTAATT[C/T]TGGATTTTTTGTAGA | 388795 |
rs563789127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898001 | CCCAGCCAGCCCCTT[C/T]GACTGCGCGTCATCT | 388795 |
rs563789547 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892390 | TGGGGCCCCCAGAAA[C/G]CCTCCTTGGAAAGAT | 388795 |
rs563798460 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860322 | TAAAAGCAAAAAAAA[A/C]CCCAGTTATTTTGTA | 388795 |
rs563846859 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950373 | AGAAAGAGGTTTGAA[G/T]AGACACTTCACCAAA | 388795 |
rs563906944 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881819 | TTTATTTTTAACCCC[C/T]ATTTTGCCAGATGGG | 388795 |
rs563966827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869349 | CAAGCGATTCTCCTG[C/T]CTCAGCCTCCCAAGT | 388795 |
rs563981552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867016 | TCCACCTCCTGGGTT[C/T]GAGTGATTCTCCTGC | 388795 |
rs563982771 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948585 | AAGAAAGAAAGAAAA[A/G]AAAGGAAAAGAAAGC | 388795 |
rs564024080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899911 | GGCTTCTACTGTGCC[A/G]TTTACTGTGGATAAA | 388795 |
rs564036669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909803 | AGACAAGCTCTCTGC[C/T]CCTTTCCTCACCTAC | 388795 |
rs564041875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905195 | ATCCTGACCCCTGTG[C/T]GGGAGGAGTAATATT | 388795 |
rs564078773 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911897 | CAGGTAACAGTGCCT[A/G]GACTAATGGGTTTCC | 388795 |
rs564122892 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938946 | CTTCCTTCCCTCCCT[C/G]CCTTCCTTCCTTCCT | 388795 |
rs564134763 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865894 | GTCTTAGTGGTGGTC[A/T]TTGTACTTGTCCCAG | 388795 |
rs564157945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938213 | AAAAAACAAAAGCCA[C/T]ATGATTATGCCAATA | 388795 |
rs564166379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940111 | TACAAGGGATATAGA[C/T]AGTAAGAAAAAAATC | 388795 |
rs564179694 | snp | C/G | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32875928 | TCTCTCTTTGAAGCC[C/G]TGGGCATGGACGCCT | 388795 |
rs564199672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955404 | ACTTAGCTGGGCATG[A/G]AAGTGTGCACCTGTA | 388795 |
rs564221000 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910857 | ATTCTCCTGCCTCAG[C/G]CTCCCGAGTAGCTGG | 388795 |
rs564240737 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899205 | CCTGGCTAACATGGC[A/G]AAACCCCGTCTCTAC | 388795 |
rs564269501 | snp | C/G | 0.000385468 | 0.0138775 | missense | EFCAB8 | GRCh38.p7 | 20:32918537 | CAGTGATGCGGTGCC[C/G]GAGAGACAAGGAGCC | 388795 |
rs564273464 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917999 | TGGAAGCTACTGCAG[C/G]GGGGCTCTGGTAGGT | 388795 |
rs564285036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931736 | GCATTCCAGCCTGGG[C/T]GACAGAGCAAGACTT | 388795 |
rs564311933 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923977 | AGCTTTTGCTATCTT[G/T]CATTATGTTTCAGTG | 388795 |
rs564340466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913726 | ACACGTTATGTACTT[C/T]CAAAATAGAATGGTG | 388795 |
rs564348543 | snp | G/T | 0.000798403 | 0.0199641 | splice-donor-variant | EFCAB8 | GRCh38.p7 | 20:32909932 | AAGATCTTTAAGCAG[G/T]TGAGTGGCCCAGGGC | 388795 |
rs564357331 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904045 | CTGAGGCAGGGTGTC[A/G]TTCTGTTGCCCAGGC | 388795 |
rs564401594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911404 | TGGAGGGGAGGGGCC[A/G]AGGCAGGCTGGAGAC | 388795 |
rs564420597 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875403 | CGTCTTTGGCTGGAG[C/G]CATCTCCCTTCTGTG | 388795 |
rs564436508 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892990 | GGATTACTGGTGCCC[A/G]CCACCACGCTTGGCT | 388795 |
rs564447447 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893509 | ACGAGGGCTGGGGAG[A/T]GGGGTGGCCTCTCTG | 388795 |
rs564519371 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945152 | AGAATTTCTGTTATT[A/G/T]TTATTATTATTATTA | 388795 |
rs564522185 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877712 | CCATGTTTTCCAGCA[A/G]CTGGGCAGTGGAATG | 388795 |
rs564556907 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953580 | CTAATGATTCATGAG[C/G]TTGGCAATCATCTTT | 388795 |
rs564583511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886479 | CAGATGAAGGGCTTT[C/T]TGAGCCTGTGTAACT | 388795 |
rs564592846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887304 | TACAGCGCCAGGCGC[A/G]GAGGCTCACGCCTGT | 388795 |
rs564593602 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877602 | GCAATTTAACCCCCT[C/T]GCATTCCTAGCATTC | 388795 |
rs564596960 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901627 | GCTCAGGCGTGCTCC[C/T]GCGCCAGGGCCTTTG | 388795 |
rs564613359 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928944 | ATCAATTAAGATGAT[C/T]GTGTGGGTTTTTTTC | 388795 |
rs564682598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916364 | CTGGGCTCAAGTGAT[C/T]CTCCTGCCTCAGCCT | 388795 |
rs564698429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954305 | TGAGTTCATTTTTGT[A/G]TATGGCATAAAATAA | 388795 |
rs564698910 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891009 | ATCTGTGACCCGCCT[A/G]GGCTTTCCACTGCAA | 388795 |
rs564707268 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953344 | TTGGATAAATACCCA[C/G]TAGTGGGATTGCTGG | 388795 |
rs564713588 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867106 | TGTATTTTTAGTAGA[C/T]GTGGGTTTCTACCAT | 388795 |
rs564736307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861434 | GCTGGGATTACAGGC[A/G]TCCACCACCACACCC | 388795 |
rs564747984 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922300 | ACTAGTGTGAGTATA[G/T]TGAGAGGACGGATTC | 388795 |
rs564820912 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950624 | GGGAGAGTTGTGTGT[C/T]TGTTCCCATACATCT | 388795 |
rs564821233 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886097 | CTGGAGCCCAAATCC[A/C]AGGGTCAGAGTCCTA | 388795 |
rs564846023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872981 | CCTGTAATCCCAGCT[A/G]CTTGGGAGGCCGAGG | 388795 |
rs564855973 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891365 | TGGGATTACAGGTGC[A/G]CGCTACCACACCCAG | 388795 |
rs564948124 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960807 | TGGTGTGAGATGGAT[G/T]GCTCCAAGGAGCTCT | 388795 |
rs564990351 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915068 | ATGCCTTGCTAATTA[A/C]AAAAAAAATTTTTTT | 388795 |
rs565016441 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928173 | ACACTATTGTCAATG[A/G]AATTATTTTTGTAAT | 388795 |
rs565048469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897107 | GCCTTCAGGCCGCGG[A/G]GCTCTCCCCTAAGGT | 388795 |
rs565095493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935779 | CAAAGTGCTGGGATT[A/G]CAAGAGTGAGTGCAC | 388795 |
rs565097926 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860167 | ACGAAAGTTAGCTGG[A/G]CATGGTGGCGTGCAC | 388795 |
rs565105742 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944319 | AAAATACAAAAATTA[A/G]CCAGGCATGGTGGTG | 388795 |
rs565168976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959409 | GCTTCCATCAAGGCA[C/T]ACATCTTGACAGTAC | 388795 |
rs565200625 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859649 | CTTCCCTTTGTCCAG[A/T]TAGACTAATTGTGAA | 388795 |
rs565248359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908562 | GGCCTGTGAGGGGCC[A/G]TGTCTTGGGATTTCC | 388795 |
rs565336550 | snp | C/T | 0.00119737 | 0.0244387 | missense | EFCAB8 | GRCh38.p7 | 20:32943675 | CTGGTTCCCCCCACG[C/T]TCCTGATGACCTGGA | 388795 |
rs565384023 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884903 | GGAAGCAACCCACAG[A/T]GGGGAGCATCAAAGC | 388795 |
rs565456766 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878231 | TGATCACACCATTGC[A/C]CTCCAGCCTGGGTGA | 388795 |
rs565469307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897347 | TAAAATAGTACCCTG[C/T]GCTTGGTGGGCTCCC | 388795 |
rs565502122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902209 | GTGTGGTCTGGCTTA[C/T]ATGTTGCAGGTGGAG | 388795 |
rs565504836 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897281 | TCACCTTCACGAGAT[C/T]GACAGCTCCTCAACG | 388795 |
rs565507708 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937701 | TTGACTCACTGCAAC[C/T]TCTGCCTCCGGGGTT | 388795 |
rs565528884 | snp | A/G | 0.000267869 | 0.0115699 | missense | EFCAB8 | GRCh38.p7 | 20:32878740 | ATGCGTGAGTTCCAG[A/G]GAAAAGAGGACATGC | 388795 |
rs565544896 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958977 | CCTGATTTGCAGGGA[A/G]GAGCAGGCTGCTGGC | 388795 |
rs565574213 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879236 | GAATAGGAGTTTCCT[C/G]CCAGGCAACAGGAAG | 388795 |
rs565584800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946961 | TTGTTGAACGTATCA[A/G]TAGTTTGTTCTTTTT | 388795 |
rs565601464 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936850 | TCTATAAGAAATGAC[A/C]TTGGAATTTTGATAG | 388795 |
rs565602603 | in-del | -/AG | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948579 | GAAAGAAAGAAAGAA[-/AG]AAAAGAAAGGAAAAG | 388795 |
rs565614892 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929211 | CATAGAATGAGTTAG[G/T]AAGTGTTATCTCCTC | 388795 |
rs565622225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914360 | GATGATCTCTGAGTT[A/G]CCTTCAGGGTCATTC | 388795 |
rs565629458 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891738 | AGAGGAGGGCGAGAG[G/T]CTGCCGTTCAGATGC | 388795 |
rs565661455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879730 | TTCAGATTCTTGTCC[A/G]TGTCCCTGTGTCTTT | 388795 |
rs565676682 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927348 | TTATTTATTTATTTA[A/T]TTTAAAATTTTTTTG | 388795 |
rs565684165 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938688 | ACTTATAATCGCATC[-/A]AAAAAATACTTAGGA | 388795 |
rs565684996 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948505 | AAAATCTGACAAAGA[C/T]GTTATAAGAAGAAAG | 388795 |
rs565716018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866603 | GGGTCTGTATGAGCA[C/T]TGGTGTGTTGGCAGG | 388795 |
rs565718470 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952971 | TCATTGAACATACTC[C/T]TCCATTTCCCGTTAC | 388795 |
rs565733986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945292 | TCCTGAGTAGCTGGG[A/G]CTACAGGTGCATGCC | 388795 |
rs565745806 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903706 | TTGATTTTTAGAGGA[A/G]TCCTTGTGTCTCTGG | 388795 |
rs565752646 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime | EFCAB8 | GRCh38.p7 | 20:32860998 | TCCCACCTTGGCCTC[A/C]AGTGTTGGCATTACA | 388795 |
rs565775624 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953503 | TGTTATTTTGTTTTT[G/T]TTTTTTTTGTTTGAA | 388795 |
rs565813313 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885738 | GAGCCAGGCAGATTC[A/T]TGGTCTAAGCAGCCT | 388795 |
rs565840852 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937200 | GGTCAGGCTGGTCTC[A/G]AACTCCAGACCTCAG | 388795 |
rs565853013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885338 | ATCCAGTAGAAACCC[A/G]CTTGGAAGAGCCAGC | 388795 |
rs565858168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872671 | TGGTGGTGGGTGCCT[A/G]TAGTTCCAGCTACTT | 388795 |
rs565874329 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908959 | GAGGACAGGAAAGAT[A/T]GGGACAAGCACGAGG | 388795 |
rs565895956 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921759 | GCCATATGCTTTTTT[C/G]TGTAAGTCTATAGCA | 388795 |
rs565977013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935388 | TATTTTCAGTAGAGA[C/T]GAGGTGTCACCTTGT | 388795 |
rs565979650 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959031 | TCATCTCCTACCCAC[G/T]CCATCCACTGCATCT | 388795 |
rs565981524 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864488 | TCCAGAGGCTGAGGT[A/G]GGGGGATTGCTTGAG | 388795 |
rs566015233 | snp | A/G/T | 0.00239393 | 0.0345281 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896713 | GACCACATCTCTGTG[A/G/T]CCATGCCCCTCTCAC | 388795 |
rs566064172 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935883 | TTGTGGATGTTACTC[C/T]CTTATCAGATGTATG | 388795 |
rs566067081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928218 | GTTCAACGTTAGTGT[A/G]TAGAAATGCAACTGA | 388795 |
rs566130182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928916 | TTTTTAATTTTGTCA[A/G]ATCGTTTTCTGCATC | 388795 |
rs566146879 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926779 | GGTTTTTTGTTCTTG[A/C]GATAGTTTACTGAGA | 388795 |
rs566154650 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922178 | TAACTTGGATGCATC[A/G]GGAACTGTGAAGCTG | 388795 |
rs566230387 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879435 | CTGAACCCTTGCTTT[G/T]CAGGGGAGGAAAACT | 388795 |
rs566231327 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875862 | ACACTTGAGAACTCC[A/G]TGGCAGTGATGGGCC | 388795 |
rs566244412 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900972 | CTCCCAAAGTGCTGG[G/T]ATTACAGGCATGAGC | 388795 |
rs566244439 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897400 | ATGAATGAATGACGC[A/C]CTCAGGGCGGTCTGG | 388795 |
rs566246013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908046 | CTGGGGGCAGGCTGG[A/G]GGTGGAGCTGTGCCC | 388795 |
rs566320942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920263 | AGCTGGGGAGTGGGC[A/G]GTCAGGATTGGGTGG | 388795 |
rs566327609 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933848 | CCAGGCATGGTGATG[C/T]GTGCCTGTAATCCCA | 388795 |
rs566401499 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901567 | GCCTGCTGCCTTCCT[A/G]ACCTCATTGCCTCCA | 388795 |
rs566497398 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905705 | GTGGAGGTTGCAGTG[A/C]GCCAAGATCGCACCA | 388795 |
rs566572880 | in-del | -/TC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866852 | CTTCCTTCCTTTCTT[-/TC]TCTCTCTCTTTCTTT | 388795 |
rs566750324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883686 | AGGTCAAGCCTTCAC[C/T]GGTCTATTTCTTTTT | 388795 |
rs566866666 | snp | A/C/T | 0.000185327 | 0.00962473 | synonymous-codon, missense | EFCAB8 | GRCh38.p7 | 20:32911609 | CTGGATGAGTCAGAG[A/C/T]GGTGCCTGCTCACAG | 388795 |
rs566871637 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937465 | TCAGAAAGACACAAA[C/T]TACTAAAGCTGACTT | 388795 |
rs566919626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956376 | GAGTTCTAGGATTCT[A/G]TCTGCAGTTGTTTTC | 388795 |
rs566930444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924890 | GTACTGTCTCCCACC[C/T]GCACCACTCCTTGAG | 388795 |
rs566944723 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894418 | TGAGCTGCCCACTTA[A/G]CTGCTTGAGCCTAGT | 388795 |
rs566965352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948220 | AACTTTATACAATAA[A/G]TTTGGCAACTTATAT | 388795 |
rs566981223 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899530 | CCTCCTTATTCAATC[A/G]CCATTCCCTGACCCA | 388795 |
rs566987025 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863197 | TGGGACTTGCTGACG[A/C]GGTGGATTGGTGCTC | 388795 |
rs567001745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951156 | GTTTCTTAAAAAGTT[A/G]AATGTGCCCCTATGA | 388795 |
rs567033852 | snp | C/T | 0.00578245 | 0.0534583 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918320 | CTGAATTTACCTCTA[C/T]GACATTGCAGTGCCT | 388795 |
rs567039455 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912221 | GCAGGGGGATCACCT[C/G]AGGCCAGGAGTTCGA | 388795 |
rs567041504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876194 | GGGGACTTGCCTGGT[C/G]GAGACGTCCCTCCTA | 388795 |
rs567143373 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869184 | CACCAACAGAGCTGT[C/T]TGCAAGGCTCAAGCC | 388795 |
rs567153908 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875640 | CTCCCAAGTAGCTGG[G/T]ATTGCAGGTACCCAC | 388795 |
rs567169827 | in-del | -/AT | 0.00318978 | 0.0398085 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859692 | TTTGTGTTATTATAC[-/AT]GTTACTTGTTAAACC | 388795 |
rs567183498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920324 | GGCCCGGCCTGATTC[C/T]CCCCAGTGCCCGGAA | 388795 |
rs567193903 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | EFCAB8 | GRCh38.p7 | 20:32962157 | CCCTCCTGGCTCTGC[C/T]GCTGTCAGGCTATGG | 388795 |
rs567291854 | in-del | -/T | 0.00103749 | 0.0227523 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889278 | GCGTCCCAGCCCATC[-/T]CCTCTGCTCTTCCTC | 388795 |
rs567293781 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900497 | TCCCTAGTAGCTGGG[A/C]CTACAGGCACGTGCC | 388795 |
rs567304791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889840 | AACCCCGCCTCTACT[A/G]AAAATACAAAAGTTA | 388795 |
rs567310946 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867237 | CTGGGGTTCTGAATT[A/C]TGACCACTGAAGATT | 388795 |
rs567334302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959531 | AGCCAGATCGGGTGT[C/T]AGGTCTGCATGGTGG | 388795 |
rs567362831 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871440 | TACCACATCCAGCTA[A/G]TTTTTTCATTTTTAT | 388795 |
rs567418163 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946668 | TATAATTTACATCCA[A/G]TAAAAGCACCTTTTA | 388795 |
rs567433064 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894948 | CCCTCCCTGGGACTT[-/A]ACTTTGCAAGCTTCC | 388795 |
rs567444424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935204 | TTTCTTTTTTTTTTT[C/T]TTTTTTTTTTTTTGA | 388795 |
rs567449563 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900851 | GGGATTACAGGCGTG[A/T]GCCACCATGCCCGGC | 388795 |
rs567491520 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893683 | GTGGCGAGGAGGCAT[A/G]TGCTCTCCTTGGCTC | 388795 |
rs567517689 | snp | A/C | | | missense | EFCAB8 | GRCh38.p7 | 20:32960091 | TGGGAGCGGCGTATA[A/C]GCCCAAGGAACGCTT | 388795 |
rs567561398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877943 | CTGCTGTGCTCTTTC[A/G]GTGAATGCTGCGAGT | 388795 |
rs567562084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906729 | CACAGCATCTGGCCT[C/T]TGTCTGGCTTCCTCT | 388795 |
rs567568104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937647 | TTGTTGAGACAGAGT[C/T]TCACTCTATTGCCCA | 388795 |
rs567569270 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890250 | TGGTAGGTGCTGTGG[A/C]CTGGGTCTCTGTGCT | 388795 |
rs567573337 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897244 | CAGCTTTGTGTGGTC[C/T]GACCATTGATTCCTC | 388795 |
rs567598215 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863639 | GCTCATCCACTGCTC[A/G]CTGGGAGTGTCCATG | 388795 |
rs567610764 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955711 | CAAGCATATATCTTC[G/T]GTTCCACGTCCTGAG | 388795 |
rs567641051 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876890 | GGAGGATTGTTTGAG[A/C]CCAGGAGGTTGAGGC | 388795 |
rs567690151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958303 | TCAACATTTGAGTGA[A/G]TGTGGGGGCTGAGGA | 388795 |
rs567706136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949575 | CAATGGAATGGCACA[A/G]AAAGTCCAGAGATAT | 388795 |
rs567727881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942357 | CCTACTTTTCTATTG[C/T]GGTAACTATCTTTTA | 388795 |
rs567762976 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950103 | AGAAATCGTAGGAGA[A/T]AACCTTTGTGACCTT | 388795 |
rs567795019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882889 | TTTAGTAGAGACGGG[A/G]TTTCACCATGTTAGC | 388795 |
rs567827010 | in-del | -/TTTATT | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936015 | CTATTTTTGCTTTTA[-/TTTATT]TTTATTTTTATTTTT | 388795 |
rs567832434 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912387 | CAGTGAGCCGAGATC[C/T]CGCCATCGCACTCCA | 388795 |
rs567845040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957579 | TCTCCCAATGATCTC[A/G]TTCGGCTTTTCTATA | 388795 |
rs567845755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919680 | TTTTTTGTATTTTTA[C/T]TGGAGACGGGGTTTC | 388795 |
rs567951641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933075 | TATATATGCATTCAT[C/T]AATCTCCATAATGAC | 388795 |
rs567952028 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946362 | TTACAAGTGAGCACT[A/G]TGAATTTTCCTACTG | 388795 |
rs567952171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955438 | CCAGTGACTCAGGAG[A/G]CTGAGGCAGGAGGAT | 388795 |
rs568005370 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888162 | TCAACCTCCTGGGGT[A/C]AAGGGATCTTTCCAC | 388795 |
rs568015222 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946928 | CACTTAGCATAATCA[A/T]TTTGAGATTCATCTT | 388795 |
rs568074195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932337 | AGCCTAGATTGCTCC[A/G]TTGCCCTCCAGCCTG | 388795 |
rs568079206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888682 | CGATAATGGAAGCAT[A/G]TTATAATGTTGCTTT | 388795 |
rs568123719 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924958 | AGTGAAGCATTTTAG[C/G]GTGGTGCCCTGGAGA | 388795 |
rs568126862 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923689 | ATATTTTTCACTGGA[A/T]AATATCATATTGCAT | 388795 |
rs568139405 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909097 | GATGCGGGGGCCGCT[C/T]GTGCTTGAGCTCCAC | 388795 |
rs568149954 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862375 | GCAAGCGATCCTCCC[A/G]CCTCGGCCTATTTTT | 388795 |
rs568172395 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900286 | CCGAAGCTTAGGGAG[A/G]GGAAGTGACTGTCTT | 388795 |
rs568191096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954770 | TTGAATTCTGTCAAA[C/T]GCTTTTTCTGCTTCT | 388795 |
rs568202589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906099 | TGCATGGGGACCACA[C/T]GTAGCCAGGGTGGGG | 388795 |
rs568226668 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904800 | CCTGGCTAATTTTTG[A/T]ATTTTTAGTAGAGGC | 388795 |
rs568263800 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904335 | GGACAGGTTCTTGCT[C/G]TGTCCCCCAGGCTGG | 388795 |
rs568275178 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863195 | GGTGGGACTTGCTGA[C/T]GAGGTGGATTGGTGC | 388795 |
rs568295078 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861741 | CCATCTCAAAAGATC[A/G]CCATGAACCCTTTTT | 388795 |
rs568335165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893814 | GAGCACCCCTTGCTG[A/G]GCGCTTTGCATGCAT | 388795 |
rs568355875 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899338 | TGAACCCAGGAGGTG[A/G]AGCTTGCAGTGAGCC | 388795 |
rs568377107 | snp | A/G | 0.000114045 | 0.00755045 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32931204 | CAAGGATTACTGCGC[A/G]TTGATTGATAAACAG | 388795 |
rs568418980 | snp | C/T | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32917372 | AGGACATCCTGAGCA[C/T]GGCCAAGTACCGGAA | 388795 |
rs568439179 | in-del | -/TAT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944160 | GTAAATACATACCCA[-/TAT]TATAGCCACCGTTCA | 388795 |
rs568442849 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | EFCAB8 | GRCh38.p7 | 20:32961860 | GTTGGGCTGTGTGTT[C/G]CTTGCCCCCTTAGGT | 388795 |
rs568459373 | in-del | -/T | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859584 | TTACAAAATATTTAG[-/T]TTTGAAATAATTAAA | 388795 |
rs568479221 | snp | G/T | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860763 | TTTTTTTGAGACAAG[G/T]TCTCATTCTCTCACC | 388795 |
rs568507396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881263 | ATGCAGTGGTGCGGT[C/T]TTAGCTCACTGCAAC | 388795 |
rs568527305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875418 | CCATCTCCCTTCTGT[A/G]CCCCCTGCAGTGGAC | 388795 |
rs568559824 | snp | C/T | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32961365 | TATCTGTCACTGCCT[C/T]AGCCTCCAGGCTGCT | 388795 |
rs568578707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958082 | GATGGGTGTCTGACC[A/G]TTTTATGCCATTGCC | 388795 |
rs568590411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875112 | TTGTTAATTGTATGG[A/G]AATGGGAGTTGGTCT | 388795 |
rs568594934 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892777 | ACTGCCCTTGCTTCC[A/C]AGGAGGAGGGAAGCT | 388795 |
rs568637602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887338 | CCCAGCACTTTGGGA[A/G]GCTGAGGCAGGCGGA | 388795 |
rs568674290 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893043 | ATGAGGTTTCACCAC[A/G]TTGGCCAGGCTGGTC | 388795 |
rs568706623 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940414 | GACTCCTACCTCATA[A/T]CACATACAAAAATTA | 388795 |
rs568745437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947916 | ATTAAAAAAAAAAAA[A/G]AAGAAAAAAGAAACT | 388795 |
rs568752483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886921 | GATCTTGGGTGCAGG[C/T]CACTGAAACTCCCTA | 388795 |
rs568780113 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941145 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 388795 |
rs568795381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882917 | AGCCAGGATAGTCTC[A/G]ATCTCCTGACCTCAT | 388795 |
rs568829627 | snp | C/T | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32889355 | GTCATTGACATGGTA[C/T]GTCTGCACAATATGA | 388795 |
rs568866969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925250 | TTTGAGATGGAGTCT[C/T]ACTCTGTTGTCCAGG | 388795 |
rs568932800 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918172 | TCCTGCCTGTGGGTA[C/T]TCAGGGCATTGCAGC | 388795 |
rs568953936 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861873 | TCCAGGCTCTTTTTT[A/C]TGCATGTGCCAATAT | 388795 |
rs568964536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905621 | AAAAATTAGCCAGGC[A/G]TGGTGGTGTGTACCT | 388795 |
rs569045932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898984 | AGGGAATCCTCTGTG[A/G]TATGTGTTCAGTAAC | 388795 |
rs569053831 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912174 | CCAGGCAGTGGCTCA[C/T]GCCTGTAATCTCAGC | 388795 |
rs569074335 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954734 | TTAGCCAAGAGAGTT[-/A]AAAAAAATCATAAAT | 388795 |
rs569090772 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933197 | CTGAGACTAAACCTA[A/G]GTCTGTCTGACTCCA | 388795 |
rs569119741 | in-del | -/GG | 0.00438332 | 0.0466095 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907469 | CCAGGGCTCCCACTT[-/GG]GACCCGCCACTGTGC | 388795 |
rs569168541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894745 | CTTTGGTATAAGAAA[C/T]GTGGAACGTTAGGCA | 388795 |
rs569211070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894372 | GCTGGCACCCTGCTT[A/G]CCTCATTGGCCTCGG | 388795 |
rs569256133 | snp | C/T | | | utr-variant-3-prime | EFCAB8 | GRCh38.p7 | 20:32961767 | CCTGTCTCCTAATCT[C/T]GTCTTCTCTCTGGCC | 388795 |
rs569259170 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861023 | ATTACAGGTATGAGC[C/T]ACTGTGCCTGGCCTG | 388795 |
rs569288074 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862565 | CTGTTGCCAAGACAC[G/T]GCTAGATTAGAGCAT | 388795 |
rs569304819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875578 | GGTGCGATCTCAGCT[C/T]ACTGCAACCTCTGCC | 388795 |
rs569329374 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869516 | GCTGGGATTACAGGC[A/G]TGAGCTGCTGTGCCT | 388795 |
rs569339125 | in-del | -/TG | 0.00318978 | 0.0398085 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859519 | TTGGCGTTTTACCTC[-/TG]TTCATGAACATACAT | 388795 |
rs569407894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924285 | CCCAGGCTAGTCTTG[A/G]CCTTCTGGGCTCAAG | 388795 |
rs569431742 | snp | C/G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935234 | AGATGGCGTTTTGCT[C/G/T]TTGTTGCCCGGGCTG | 388795 |
rs569431944 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882005 | CTGAGGTCAGGAGTC[C/G]TGGCCAACATGGTGA | 388795 |
rs569444513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892844 | CTCTTTTTTTTTTTT[C/T]TTTCTTTTTTTTATG | 388795 |
rs569465298 | snp | A/G | 0.000110945 | 0.00744715 | missense | EFCAB8 | GRCh38.p7 | 20:32931311 | GGACCAACTTCCCAC[A/G]CTACATTCCCTTGGA | 388795 |
rs569470887 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922785 | GCCCACATGGGAGAG[C/G]TGGCATGGAATGTTC | 388795 |
rs569523885 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904178 | TTAATTTTTTTGTAC[A/T]GATGGGATCTTGCTG | 388795 |
rs569533917 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861581 | GATGTGAGCCACCGC[A/G]CCTAGCCGTTGAAAC | 388795 |
rs569545224 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873315 | CCATCTCTTGACCTC[G/T]TGATCCACCTGCCTC | 388795 |
rs569561397 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904587 | TGCAGGTGTGAGCCA[C/T]CACACCTGAATGGAG | 388795 |
rs569573612 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867265 | ATTTGAAATGATATA[C/G]TTACTGAACTGAGGT | 388795 |
rs569593059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954509 | TTTTTATGCCTGTAC[C/T]ACACTGTCTTGATTC | 388795 |
rs569631560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866746 | TCCTTCCTTCCTTCC[C/T]TCCCTCCCTCCCCCT | 388795 |
rs569634028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954354 | TTGCATGTGGCAATT[C/T]GGTTTTCCCAAAACC | 388795 |
rs569634950 | in-del | -/CCTT | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938947 | TTCCTTCCCTCCCTC[-/CCTT]CCTTCCTTCCTTTCT | 388795 |
rs569645392 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903550 | ATCAATACGTGAAAT[C/T]GGCCTGAAATAATTT | 388795 |
rs569658664 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902356 | TGTATTTTTGGGGTA[A/G]GGTAGAGAATATATT | 388795 |
rs569714378 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927957 | TCATCTTGTTAAATT[A/G]AAACTATACCCATTA | 388795 |
rs569733686 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909606 | TTCTAGGAACACTAG[G/T]GTTTGGAAGGCTCAG | 388795 |
rs569770244 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946126 | CGGCAGGAGGGACTC[A/T]GATAGTGTGTGCTAG | 388795 |
rs569772179 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937859 | CCCAACCTCGTGATC[C/T]GCCCACCATGGCCTC | 388795 |
rs569797294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960594 | ACGGAGTGGCTCTCC[A/G]TCAGGGACAGAAAGG | 388795 |
rs569911172 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953841 | TTGAAATGGAGGTTT[C/G/T]CTCTTGTTACCCAGG | 388795 |
rs569948402 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960974 | GTGGATGCATGGGCC[C/T]GCAGGCCACGGTGGT | 388795 |
rs569958645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951998 | GGCATGGTGGCTCAC[A/G]CCTGTAATACCAGCA | 388795 |
rs569982632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944465 | GTGAGACTCTGTCTA[A/G]AAAAAAAATAATAAT | 388795 |
rs569984081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928945 | TCAATTAAGATGATC[A/G]TGTGGGTTTTTTTCT | 388795 |
rs570018258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943971 | ATTATCCATTCAGCA[A/G]ACGGTCCATCCATTC | 388795 |
rs570128796 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879752 | TGTGTCTTTGGGCAC[C/T]CCTCACATGAGTCTT | 388795 |
rs570147256 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897766 | TCCCTCCAGGTCTCA[C/T]TCAGTGTCTTGGATT | 388795 |
rs570153161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886252 | TGACATAATACATGT[A/G]TAGTGCTTGGGGCAG | 388795 |
rs570199882 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859361 | TCTCCAATTCTAAAT[A/G]TCAACCGAGTTTTAC | 388795 |
rs570220362 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936032 | TATTTTTATTTTTAT[G/T]TTTATTTTTTATTTT | 388795 |
rs570270491 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901837 | GGATTACAGGCACGC[A/G]CCATCATGCCCGGCT | 388795 |
rs570326328 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905738 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC | 388795 |
rs570357443 | snp | A/G | 0.000798403 | 0.0199641 | missense | EFCAB8 | GRCh38.p7 | 20:32961328 | AGCACGCCTGCGGCC[A/G]CCTCCTCCCCATCTT | 388795 |
rs570360074 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897278 | CTGTCACCTTCACGA[G/T]ATCGACAGCTCCTCA | 388795 |
rs570365275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861681 | AGATGGGAGGATCAC[C/T]TGAGCCCAGGAGTGC | 388795 |
rs570396733 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896739 | CTCACTACCGCCATT[C/G]CTAAGCCCTGGTCCT | 388795 |
rs570402920 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861164 | TCATTTCTGTGTCTA[C/T]AATGGTTCACTTTTG | 388795 |
rs570429062 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868169 | GCTCAAGTGATCCTC[C/T]TGCCTTGGCCCCCGG | 388795 |
rs570460760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939385 | CCTCCCAGGTTCAAA[C/T]GATTTTCCTGCCTCA | 388795 |
rs570497734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938614 | ATATAAATATACAAA[A/G]CCAATATATTTATAT | 388795 |
rs570513585 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903034 | CTTAGCAGCCTCACC[A/G]TGTCCCCTCAGGCCA | 388795 |
rs570522085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932240 | AAATCAGCTGGGTGT[A/G]GCGGTGCACGCCTGT | 388795 |
rs570580976 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875005 | CTTCCCGCCTCTGCC[A/T]CCCAGAGTGCTGGGA | 388795 |
rs570604366 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953935 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGCTTA | 388795 |
rs570628009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903614 | ATTTTTCGGCAGCAC[A/G]TATACGTGTGGAGGG | 388795 |
rs570768591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937644 | TTTTTGTTGAGACAG[A/G]GTCTCACTCTATTGC | 388795 |
rs570774186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922553 | AAAATAAAGGGCATG[C/T]CACAGAGTGAGTGAG | 388795 |
rs570788194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904245 | GGATCCTCCTGCCTC[A/G]ACCTGCCAAAGTGCT | 388795 |
rs570805749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923283 | CTGAGCTCAGGAGTT[C/T]GAAACCAGCCTGGGC | 388795 |
rs570820841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886790 | AGCAGGCCTGGATTC[C/T]TCCTGGAGGGGCCGC | 388795 |
rs570860116 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900171 | GGGCCATTTAGACCC[A/C]TGTCTGTCCCTTTCT | 388795 |
rs570894279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908817 | AGTCATGAACTTTGG[A/G]AAACAGGGGCCACGT | 388795 |
rs570913811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874048 | AGCTCAACCTCCCCA[A/G]TAGTTGGGACTACAG | 388795 |
rs570914862 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915193 | AGGCATGTACCACTG[C/T]TCCTGGATTCTGCTT | 388795 |
rs570925989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880356 | TCACTGCAACCTCCG[C/T]CCCCCGGGTTCAAGC | 388795 |
rs570968864 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916763 | TTTATAATTATAAAG[A/T]ATATTCAGTGCTGTG | 388795 |
rs571052063 | in-del | -/AAA/AAAAAAAAAAAAAAA | 0.496348 | 0.0425753 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905759 | GTGAGACTCCATCTC[-/AAA/AAAAAAAAAAAAAAA]AAAAAAAAAAAAAAG | 388795 |
rs571058861 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926511 | CTATCCACTTCATTC[-/T]TTTTTTTTTTTATTA | 388795 |
rs571105832 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899763 | ATTTTTAGTAGAGAC[C/G]GGGTTTCTCTGTGTT | 388795 |
rs571159997 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886365 | CTCAGGAGAACCCAC[C/T]GTGTACTTGGTCGCC | 388795 |
rs571161853 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892627 | TAACAAAGGGCAGCT[A/G]GAGGACTAGGGATTC | 388795 |
rs571199599 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891660 | TTGTGGCCCCAGCCC[A/T]GTCCAGCCAGTGCTC | 388795 |
rs571218756 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890980 | TCAGCCGTCAGCAAG[A/G]GCTAGAGCAATCTAT | 388795 |
rs571224997 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944041 | CAAATCATATATCTG[A/C]TAAAGCATATTCCTT | 388795 |
rs571261720 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952107 | TTCTACAAAAAAAAA[A/T]ATTAAAAATTAGCCA | 388795 |
rs571282125 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895633 | CTGGAGTGCAATGGT[A/G]CGATCTTGGCTCACT | 388795 |
rs571289475 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952889 | GTTCAGTAGTGTTAA[A/G]TATATTCACATTGTT | 388795 |
rs571307534 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865761 | CTGAGATCGCACCAC[A/G]CTCCAGCTGGGTGAC | 388795 |
rs571313789 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959687 | ATTGGAAAGGATCAG[C/G]CCAGGAAGGGGAGAG | 388795 |
rs571319682 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866387 | AGGTCATCTAATTAT[A/C]CACGTTAGAGTCTTT | 388795 |
rs571377119 | snp | A/G | 9.80248e-05 | 0.0070002 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960170 | GCATCAGGTAAGGTG[A/G]GATGGGGCAGCTCCC | 388795 |
rs571382475 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927592 | TCAGGTGATCCACCC[A/G]CCTTGGCTTCCCAAA | 388795 |
rs571401159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928609 | TAGCCCCTTTTTTTT[A/G]GTGTGGGAGCTTTAG | 388795 |
rs571404421 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890496 | TCCTCCAGACTGGAA[C/G]GTCAGGGACTGCATC | 388795 |
rs571442339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889933 | CTTGAACCTGGAGGT[A/G]GAGGTTGCAGTAAGC | 388795 |
rs571509005 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879080 | TAGGTAGAAAGTGGC[A/G]GGCTGCTGTGTTTGG | 388795 |
rs571538940 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873512 | TTGCCTGTTCCTCCT[C/T]TCTTCTCCCCATCTT | 388795 |
rs571559764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921670 | CTCAACAGCAGCATT[C/T]GCTGCTAACAGGTTG | 388795 |
rs571562441 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900937 | TCGATCTCTTGACCT[C/T]GTGATCCGCCCACCT | 388795 |
rs571564250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864346 | CCCAGCACTTTGTGA[A/G]GTGAAGGCAGGAGGA | 388795 |
rs571565525 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954127 | CGTTTTTTGATACAC[-/AG]AGGTTTTCAAGTTTA | 388795 |
rs571588043 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918958 | GGGAGCCATGGGGTC[C/T]CACCTGCTTGGAGAC | 388795 |
rs571590483 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901494 | TTTATTGAGTCCTGA[C/T]GGCAGGAGGATATCA | 388795 |
rs571598994 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871794 | CATGCCAGTGTCCTT[C/T]TTCCTGTTCTGTAAG | 388795 |
rs571600216 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960845 | TGGGCCTCACCCAGG[C/G]TCCAGCTCGAGGCCT | 388795 |
rs571622655 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871127 | AAAGTTCTGGGATTT[C/T]AGGTGTGAGCCACCG | 388795 |
rs571626431 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863692 | CCTTGACCTTGACTT[C/G]TTTTCCACCTTTCTG | 388795 |
rs571663595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943118 | TAATGTGATTTATCA[C/T]CCCATTGCTCACCCT | 388795 |
rs571663693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934800 | TCTTTCACCTCTGCC[A/G]TGATTGTGAGGCCTC | 388795 |
rs571700898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942527 | CCCCATCTCTAAAAA[A/G]AAAAACCAATAAAAA | 388795 |
rs571723280 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923221 | CCCAGTGCGATGGCT[C/T]ACACCTGTAATCCTA | 388795 |
rs571726922 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935288 | TCACTGCAACCCCCG[C/T]CTCCCGGGTTCAAGC | 388795 |
rs571750162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895955 | AGGTGTGAGCCACTG[C/T]GCCTGGCCCAGACAT | 388795 |
rs571753332 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941741 | TGACTACTGGGTAAA[C/G]AGTTTCTTTCTGGGG | 388795 |
rs571782210 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929238 | CCTCTTCAGTATTCT[C/G]GAAAAGTTTGGGAAG | 388795 |
rs571795220 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906771 | TGTCCCCACTTCTGG[A/G]CACCACCTTCACCAG | 388795 |
rs571818035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950277 | AAGATATTTGCAAAT[C/T]CTATATCTGATAAAG | 388795 |
rs571839588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877746 | TCTGGAGTTGCGCCA[A/G]TGGCCCTGGTGTGGG | 388795 |
rs571840152 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895508 | TTTTTATTTTTTTGA[-/T]TTTTTTTTTGTAGAG | 388795 |
rs571854589 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958352 | CCTTGAAGGGAGAGG[A/T]TAAGGGGCAGAGGGC | 388795 |
rs571888087 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32908322 | ATGCCTCCAGTCCTT[C/T]TGTGGGAAGTTTTTT | 388795 |
rs571913446 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920222 | GTGGAGAAGGTTGGC[C/T]GTGATCAGCCAGGGA | 388795 |
rs571924990 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907762 | CTCGCTGAGGTCCCC[A/C]GTCGGCCATGGGCAG | 388795 |
rs571985318 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935623 | GCAATTCTCCTGCCT[A/C]AGCCTCCCAAGTAGG | 388795 |
rs572048016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944131 | GAAGGGTTCAGCTTG[A/G]TGAATTTTGAGAAAG | 388795 |
rs572093437 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939149 | TCTTTCTTTCTTTCT[C/T]TCTTTCTTTCTTTCT | 388795 |
rs572109320 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936249 | ATGTTGGCCAGGCTG[C/G]TGTTGAACTCTTGAC | 388795 |
rs572167749 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872504 | AGACAAGAGTGAAAG[C/T]GAGCTGGGCACGGTG | 388795 |
rs572183130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864702 | AGGTTGTGATAATAG[C/T]GGGATGGGCTGTAAG | 388795 |
rs572205831 | snp | A/G | 0.00177578 | 0.0297445 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878671 | GACCATTTTGCCAAT[A/G]CCCTGCCTCCCTTGT | 388795 |
rs572216355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878087 | CCTGGGCAACATGGC[A/G]AAACCCCATCTCTAC | 388795 |
rs572219496 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914756 | CTCACCTCCTACCAG[G/T]TCCCTCCCTCAACAT | 388795 |
rs572221055 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959248 | TAAGTAATGAGAGTA[C/T]TAGGAACAGGGATGG | 388795 |
rs572223959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943565 | CTCTGCTGCCTGCAG[C/T]CCTGGGTGCCTTCTA | 388795 |
rs572231885 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877129 | CCTGCGTTAACTGCC[A/G]TCTCATAGCTCTCCT | 388795 |
rs572297616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898081 | TCCTTGAGCACTCCA[C/T]GCTATGACAAACATG | 388795 |
rs572328750 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865344 | AAGCACCGAATGCTT[A/G]CTGGGCTTGGGGATG | 388795 |
rs572396297 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884001 | TCAGCCTTCCAAAGT[G/T]CTGGGATTACAGGCG | 388795 |
rs572455201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921153 | GTGTTGGGAGGGAGA[A/G]CAGGAGTGGCTGCAC | 388795 |
rs572456647 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957251 | AGGGCCCACTTCTAA[C/T]GCCTATTTCTTCTCT | 388795 |
rs572558652 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958833 | GGGCCCTGTCCCCCA[G/T]CCAGGCCCAGATTTG | 388795 |
rs572563997 | snp | C/T | 0.000188573 | 0.00970828 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863746 | ACGTGGTCCTTACAA[C/T]GACTGGAGTTAAGTT | 388795 |
rs572682802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900565 | TTTTTAATTTTTATT[A/G]TTTTTATTTTTTGTT | 388795 |
rs572700564 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942709 | CCTTTGCCTGTTTAT[C/T]ACTTTCTTAGAGAAA | 388795 |
rs572725840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924693 | CCTTGGGCTTTTTAC[A/G]TGGCCTGGTGATCTG | 388795 |
rs572729225 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895683 | TTCAAGTGATTCTCC[C/T]GCCTCAGGCTCCTGA | 388795 |
rs572740577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934949 | TCCCTCCAACATTGT[A/G]CAAGGGTTTTCTTTT | 388795 |
rs572750400 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926354 | TGAAAGTTGTGTGCA[C/G]GTTAAATTTTTTTTT | 388795 |
rs572772437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912922 | GTGTTCTCTCTCCAG[A/G]TGGGTTCCTCCATTC | 388795 |
rs572778698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934044 | GTAGAGATGAGGTCT[A/G]TGTTGCCCAGGCTGG | 388795 |
rs572785741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870155 | TCTCCAGTTTACGAA[C/T]GAGTAAAGTGAGACC | 388795 |
rs572808794 | in-del | -/TGG | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958278 | GTCGTGCCTGGTGTA[-/TGG]TGGGCACTCAACATT | 388795 |
rs572912623 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890310 | CCAACAGCCTCTGCT[C/T]TTCTTTTGGCTCTCA | 388795 |
rs572916169 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933517 | AGTATGCAATATATT[-/C]ACTGACTATAGTCAC | 388795 |
rs573016880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899922 | TGCCGTTTACTGTGG[A/G]TAAACTGGTAGGTAT | 388795 |
rs573025293 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916501 | TGGCCTCAAACGATT[G/T]TCCTTCCTTGGCCCC | 388795 |
rs573027137 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882560 | AGGTCTTGCTCTGTG[A/G]CCCAGGCTAGAATGC | 388795 |
rs573051442 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876418 | AATAGGCCAGCCTGT[A/G]GCTGTTACATCTAAA | 388795 |
rs573076961 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911135 | GTTCCCTACTTAGGG[G/T]GCAGTTAGTTTATTT | 388795 |
rs573088705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913841 | CAAATGCTAGTAGAC[C/T]TTAAATCTCAAAGAT | 388795 |
rs573101893 | snp | C/T | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32875953 | ACGCCTTCATCAAGG[C/T]CATGAAGAAGGTTCT | 388795 |
rs573158562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893511 | GAGGGCTGGGGAGAG[A/G]GGTGGCCTCTCTGAG | 388795 |
rs573204809 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947057 | ACATTTGAGTCATTG[C/T]CAGTTTTGGATGATT | 388795 |
rs573228061 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939104 | TTCTTTTCCTTCCTT[C/T]CTTTCTTTCTCTCTT | 388795 |
rs573239208 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904471 | GCCCAGCTAATTTTT[A/G]TTTTTTTTGTACAGA | 388795 |
rs573257147 | in-del | -/TTCT | 0.00279162 | 0.0372561 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954905 | AGTCAAGATGTATTA[-/TTCT]TTCTTTTAATATATT | 388795 |
rs573282209 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893878 | GAGGAGCCGCTGCTG[C/G]AGCCCATAATAAGAG | 388795 |
rs573382349 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942761 | TTTGTAGGTGTTTTA[C/T]GATTTCATTGAAAAT | 388795 |
rs573417246 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950533 | TTACAGACTAAGAGT[G/T]TTTAAGGATTCAGGG | 388795 |
rs573459200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946602 | TATCCCCTAAATATA[A/G]TATCTAGTGTTATCT | 388795 |
rs573469282 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887008 | GTGGGGGTTAGACTC[C/T]AGCCCTGGGCAGGAG | 388795 |
rs573481581 | snp | G/T | 0 | 0 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868518 | TAGCATTTTGGTGTA[G/T]GTATTTTCTTCCAGT | 388795 |
rs573496380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919926 | TAAAGTGGAGGTTTC[C/T]GGGATCCACTGAGCG | 388795 |
rs573512438 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867902 | CTGGAGTGCAGTGGT[C/G]TGATCACCACGGCAG | 388795 |
rs573534658 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958637 | GGAAGCCTCTACCTG[C/G]GTTGGGTAGAGCTAG | 388795 |
rs573534900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926213 | TGGGAGAACTTTGTG[A/G]TGCATCACTTTGGTG | 388795 |
rs573538672 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940163 | GGACTCACAATTCCC[A/G]AGTTCAAAACTGAAT | 388795 |
rs573568550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907519 | TCAGGATACTGCCCC[A/G]TCTGCTGGGCTGTGG | 388795 |
rs573589541 | snp | C/T | 9.35497e-05 | 0.00683858 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32863807 | AATGTCTTCTGAAGA[C/T]TTAGCAGAGATCCCT | 388795 |
rs573653167 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912725 | TTGGCACCTTTAGGA[A/G]GACATTTAGGGCCCA | 388795 |
rs573669665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894485 | GTGGTGGTCTTTGAG[C/T]CACATGGTGAATGGG | 388795 |
rs573706195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899637 | TGGAGTGTAATGGTG[C/T]GATCTCGGCTCGCCA | 388795 |
rs573706441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894012 | TGGGCTGCATCCCAC[A/G]CTGATTAATAGCAGG | 388795 |
rs573725397 | in-del | -/GTGCTTCTCTCCT | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898631 | AAACCCAGGTAAGAA[-/GTGCTTCTCTCCT]GGCTAAGGCGGTGGG | 388795 |
rs573768965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925499 | GCTGGCATTACAGGC[A/G]TAAGCCACCACGCCT | 388795 |
rs573815502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913125 | CTGGAGTATCTATTT[C/T]AGTGGGGGAATGTCT | 388795 |
rs573824961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901033 | ACCAAACAGTGCACT[A/G]TGTACATTTCTAGAC | 388795 |
rs573948076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888347 | TCTTCTGCCTCAGCC[C/T]CCCGAGTAGCTGGAA | 388795 |
rs573989790 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870250 | ATTGTTTGCAGCCAG[G/T]AAGTGCCACCACTGT | 388795 |
rs573990108 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877281 | TGGCACGATCTTGGC[G/T]CTTTGCAACCTCTGC | 388795 |
rs573992236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940679 | ATATATCTGATAAGG[A/G]ACTAGTATCCAGAAT | 388795 |
rs574000392 | snp | A/G/T | 0.00438332 | 0.0466095 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928540 | GCACCCAGCCAATGC[A/G/T]ACTGATTTTTATGTG | 388795 |
rs574043734 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883176 | GCCTCTGTAGGCCCC[A/G]TTAGAGCATTTCTCT | 388795 |
rs574074626 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889477 | GTGCCTGGGAGAAGT[C/G]TGTTGGCTGAGCAAC | 388795 |
rs574082556 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888960 | GGTTGGTTTTTTTTG[G/T]GGGGGGCGGGGGGCG | 388795 |
rs574109193 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935918 | ACATATATTTTCTGT[C/T]ACTCTGTGGGTTATC | 388795 |
rs574177200 | snp | A/G | 0.000184264 | 0.00959677 | missense | EFCAB8 | GRCh38.p7 | 20:32911642 | TTGCGGGATGGCACA[A/G]TGAAGATGTGGAACT | 388795 |
rs574183579 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869240 | AGATGGGTGTTGCAA[A/T]TTTTTTTTTTTTTTG | 388795 |
rs574188862 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875710 | GACAGGGTTTCACCA[G/T]GTGGATCAGGCTGGT | 388795 |
rs574202679 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948457 | AGTTGAAAAGGGTAC[A/G]ATACTTCCCAACTCA | 388795 |
rs574231187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863230 | AAGACCCTAACAAAA[C/T]GCTGTCATCCATCTC | 388795 |
rs574253680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939912 | GTTGGCCAAGCTGGT[C/T]TCGAACTCCTGACCT | 388795 |
rs574257771 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911312 | CACTGCCCTGTGATA[C/T]AGGGCAGAGGAGGTC | 388795 |
rs574271079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862788 | ACCTGCCACCAAACC[C/T]GGCTAATTTTTTATA | 388795 |
rs574296103 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864493 | AGGCTGAGGTGGGGG[G/T]ATTGCTTGAGCCTGG | 388795 |
rs574385449 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880808 | CAGTCCTCTGGGGTT[G/T]TTAGTGGAAGCTTCA | 388795 |
rs574433248 | snp | C/G | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860299 | TGACAGAGTGAGACT[C/G]TCAAAAATAAAAGCA | 388795 |
rs574447901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953401 | TTTTGAGGAACCTCC[A/G]TACTGTTTTCCATAG | 388795 |
rs574469298 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868644 | GGCAGGAGTCTGGGC[A/G]TGGCTTAGCTGGCTT | 388795 |
rs574521886 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895860 | ACAGGCGTGAGCCAC[C/T]GTGCCTGGCCCAGGC | 388795 |
rs574539197 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933941 | GAGGTTGCGCCACTG[C/T]ACTTCAGCCTGGGCA | 388795 |
rs574542680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892950 | GGTTCAAGTGATTCT[C/T]CTGCCTCAGCCTCCT | 388795 |
rs574610656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931527 | ACTTTGGGAGGCTGA[A/G]GCGGGTGGATCACGA | 388795 |
rs574611178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954025 | TGGCCAGGCTGGTCT[C/T]GAACTGCAGGCCTCA | 388795 |
rs574637303 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887664 | GCCGAGTGGGCTGGC[A/C]TCCCTCTTCCCCAGG | 388795 |
rs574647327 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938663 | CTGAAAATGAAAATT[A/T]AAAAATTTCACTTAT | 388795 |
rs574680034 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930765 | GAGTCCTCTCCTGCT[C/T]TGCTAAGCCCAGTGA | 388795 |
rs574798322 | in-del | -/T | 0.0539704 | 0.155153 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910739 | CACCTCACTTGCTAC[-/T]TTTTTTTTTTTTTTT | 388795 |
rs574931213 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915592 | CTTTCTAGGCCCTCA[C/G]TGGAATCACCCTTAA | 388795 |
rs574996310 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869340 | CCTCTGGTTCAAGCG[A/T]TTCTCCTGTCTCAGC | 388795 |
rs575021368 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918758 | TTTTAGTCCCAATGT[A/G]TCTATCCTGGAGCTG | 388795 |
rs575032303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897469 | TTTGGTTGAGTCAGG[A/G]CCTTACTCTGCTGCC | 388795 |
rs575034245 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903721 | ATCCTTGTGTCTCTG[A/G]ACAGATGATTTAAAG | 388795 |
rs575039355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916229 | TCACATGGTAGAGAG[A/G]ACAAGGGATCTCTCT | 388795 |
rs575040904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872948 | AATACAAAAATTAGC[C/T]GAGTGTGATGGTGGG | 388795 |
rs575097125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875808 | GCCACCGCGCCTGGC[C/T]GTAGATGTGGTCTTC | 388795 |
rs575101194 | in-del | -/CCTTCCCTT | 0.00199481 | 0.0315187 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859383 | AGTTTTACATCTCAG[-/CCTTCCCTT]CCTTCCCTTCCTTCC | 388795 |
rs575219326 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879927 | GGGGTTGATCTGCCT[C/T]GCTGTGTGTTCCTCC | 388795 |
rs575230288 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957178 | TTAATTTTATTTAAC[A/C]TTATTTGTAACAGTT | 388795 |
rs575239903 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928597 | GAATTCATTTGTTAG[-/C]CCCTTTTTTTTGGTG | 388795 |
rs575300856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876346 | CAACCTCCCATTTGG[C/T]TTGGGGGATTCAAGC | 388795 |
rs575313715 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871517 | AAAAAATTAATTTTA[A/G]CAAGTTTACCTCTTG | 388795 |
rs575329785 | snp | C/T | 0.000284589 | 0.0119253 | missense | EFCAB8 | GRCh38.p7 | 20:32918521 | CTGGTGTCGGCTCCC[C/T]CAGTGATGCGGTGCC | 388795 |
rs575344332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946416 | TTTTTTGTTTTTTTG[A/G]TTTTTGTTTGTTTGT | 388795 |
rs575404237 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863345 | TGGCTTGCAAGGGCA[C/T]TGGAAGGTGGGTGGG | 388795 |
rs575427032 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917067 | GGTGTATTACACATT[C/G]ACTATCTGTAAGATT | 388795 |
rs575428453 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931633 | GTGGTGGTGCACTCC[C/T]TGTAATCCCAGCTAC | 388795 |
rs575446334 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882383 | CACTGTCCAAGTGTC[A/G]ACAGAACCCAGCAGC | 388795 |
rs575482273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887785 | CGAGTGCAGGATGCA[C/T]CAGTGCTGAGCTCCT | 388795 |
rs575493060 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910349 | ATTGTAGGAAGGGAC[A/G]GAGGCCCAGGCAGCA | 388795 |
rs575508409 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930776 | TGCTCTGCTAAGCCC[A/G]GTGACAGGAGCGGGT | 388795 |
rs575522341 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893501 | AGAAGACCACGAGGG[A/C]TGGGGAGAGGGGTGG | 388795 |
rs575532949 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904418 | CAATCCTCCCACCTC[A/C]GCCTTGCAAGTATTT | 388795 |
rs575594692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954994 | GTGCCCAAAACCTTC[C/T]TGGTCCTGGACATCT | 388795 |
rs575603106 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892014 | TTTTATTCCAGCTGC[A/T]GTTGGAAGCCTTTGG | 388795 |
rs575615820 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903804 | CAGGGGCCTGGGCTA[A/G]CAGTGGCCATGGGAG | 388795 |
rs575665923 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861887 | TATGCATGTGCCAAT[A/T]TGCACATGCATATAT | 388795 |
rs575701695 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922968 | GTGGGAGGACTGCTT[A/G]AGCCCAGGAGTTCTA | 388795 |
rs575712066 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898380 | TAGGAGAAGGGCATT[A/G]GACTCCGTGATCTCT | 388795 |
rs575740445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868390 | TTTGCATCTAGTGTC[C/T]CCTGTAAAACTTTCA | 388795 |
rs575874433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873493 | CGTGGAGAATTTTCT[A/G]TCCTTGCCTGTTCCT | 388795 |
rs575877866 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954173 | TTTCATTGCCTGTTT[C/T]TTTAGTGTCATATCC | 388795 |
rs575918372 | snp | C/T | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32961182 | TCAGTGATCTGATGC[C/T]GACTCAGCAGCCTGA | 388795 |
rs575940249 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932946 | ATATTAAAATGTCTT[C/G]GGAACTGATTACCCA | 388795 |
rs575978581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897091 | CCTCGGCATGTGCTG[C/T]GCCTTCAGGCCGCGG | 388795 |
rs575986308 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882577 | CCAGGCTAGAATGCA[A/G]TGGCATCATCTCAGG | 388795 |
rs576066123 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879961 | TGGACTCCCTAAGCA[C/T]GAGGAGCATTGCAGG | 388795 |
rs576094461 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930087 | GTCTGAGCCTATGTC[A/C/G]AATCAAACTTGTAAG | 388795 |
rs576101790 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925704 | ATCTCCCCAGTAGGG[A/G]AGGACCAGATGGCAC | 388795 |
rs576121210 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886457 | GGTTGATTGAGAACA[A/C]AGCCCCCAGATGAAG | 388795 |
rs576133244 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879409 | CGTGGCTCCTCCACC[C/G]GCTGTGCCCACTGAA | 388795 |
rs576134833 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872278 | CAACCACGCCTCTCT[C/G]TGCCACATTTTCTTC | 388795 |
rs576150210 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937020 | TTTTAACTTCTTGGT[A/T]AAATTTACCCCTAAG | 388795 |
rs576172117 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902358 | TATTTTTGGGGTAGG[G/T]TAGAGAATATATTTA | 388795 |
rs576212053 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860667 | GTCAGCCATTGTGCC[C/T]AGGCTATTTTTTCAT | 388795 |
rs576236073 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870422 | TTGATATACAGAGAA[A/C]ATGTTTTTCTCCCCC | 388795 |
rs576266886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953028 | ACTTTCTGTTTCTAC[A/G]AATTTAACTACTTTA | 388795 |
rs576302138 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860080 | GAAGCCAAGGCGGGC[A/G]GAAAGCACTTGAGGC | 388795 |
rs576307980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902933 | CCCCCGGCGTCTCCC[C/T]GACTGTCCCCTCTTC | 388795 |
rs576350957 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952379 | CTATAAGTTTTATAG[C/T]TTTCACTCTTACTTT | 388795 |
rs576378508 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887109 | TCCTCTGTGCTCTTG[C/G]TGCTCTCTGAGTTCT | 388795 |
rs576385299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944645 | AGCATTTCTTTAAAG[A/G]CAGGTCTAATGGTGA | 388795 |
rs576480575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959344 | GGAGTTGGGTTTTGA[C/T]ATTTAAGTAGGAGTC | 388795 |
rs576498633 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914871 | TTCCTTTCTATATGG[A/C]TAGGATGAATCTTTT | 388795 |
rs576505878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881489 | GGCGTGAGCCACCGC[A/G]TCCAGCCAGTCATCT | 388795 |
rs576517320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948678 | TAAAATCCAGCAATG[A/G]TCACATAGGGTTTAC | 388795 |
rs576538449 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923416 | GATTGAACCCGGGAG[A/G]CGGAGGTTGCAGTGA | 388795 |
rs576539874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921234 | AGGGTCTCACTGTCA[C/T]CCAGGCTAGAGTACA | 388795 |
rs576543052 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880636 | AATATGAATGATAAG[A/T]GATTTCATAACTGTA | 388795 |
rs576562012 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915407 | AAGTTCTTTGCCATT[G/T]TGTAACAAGTATGAC | 388795 |
rs576646981 | snp | A/T | 0.00330188 | 0.0404974 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928246 | TGATTTTTTATTTTT[A/T]TTTTTTTGAGACAGA | 388795 |
rs576671498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927469 | TCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 388795 |
rs576678303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932100 | TATTCAGTGGTGGGC[C/T]GGGCACGGTGGCTCA | 388795 |
rs576680070 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896222 | CTAGTTCTGCCATGC[A/C]CTGGCAGGGGCACTC | 388795 |
rs576681552 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865795 | TGAGACTCTGTCTCA[-/A]AAAAAAAAAAAAAAA | 388795 |
rs576707466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890659 | GAAATGACAGCTGGT[A/G]ATGTGAGGCTGAATG | 388795 |
rs576715091 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913998 | AGCCTTGCCCCCATG[G/T]TGGCTCTATGCCTGG | 388795 |
rs576717015 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895733 | CACACCACCATGCCC[A/G]GCTAATTTTTGTATT | 388795 |
rs576726356 | snp | A/G | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860098 | AAGCACTTGAGGCCA[A/G]GGAGTTTGAGACCAG | 388795 |
rs576736119 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881572 | TTTAATCCATTTATT[A/T]ATCTTTACCCTCAGC | 388795 |
rs576755353 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892137 | TTCCTTGGGATAGCA[A/G]TGAGGCTGCTCACTG | 388795 |
rs576762583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923424 | CCGGGAGGCGGAGGT[C/T]GCAGTGAGCTGAGAT | 388795 |
rs576785561 | snp | A/G | 0.000718219 | 0.0189366 | missense | EFCAB8 | GRCh38.p7 | 20:32959854 | GCTCTCCTGCATGGG[A/G]AGGCAGATAAGGAGG | 388795 |
rs576788199 | snp | A/G | 0.000399281 | 0.0141238 | missense | EFCAB8 | GRCh38.p7 | 20:32961322 | ACGGACAGCACGCCT[A/G]CGGCCGCCTCCTCCC | 388795 |
rs576832720 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947809 | GAAAGAGGTCTGGTG[C/T]GGTGGCTCACGCCTT | 388795 |
rs576917300 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866878 | TTCTTTCTTTCCTTC[A/C]TTCCTTCCTTTCTTT | 388795 |
rs576917335 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860169 | GAAAGTTAGCTGGGC[A/G]TGGTGGCGTGCACCT | 388795 |
rs576927456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866136 | CCTCACTATGTTCAC[A/G]GTGTATCCACAGTGC | 388795 |
rs576928854 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959004 | TGGCTACTTGGTCCT[-/C]CCCCTGCAGGTTCAT | 388795 |
rs576931376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897397 | TGAATGAATGAATGA[C/T]GCACTCAGGGCGGTC | 388795 |
rs577053754 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892900 | GGCTGGAGTGCAGTG[G/T]TGCCATCTTAGCTCA | 388795 |
rs577056568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936189 | AGGCGTGTGCCACCA[C/T]GCCTAGCTAATTTTT | 388795 |
rs577074547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945581 | TTTGTCAAATAATTA[A/G]TATACCTCAATTTCT | 388795 |
rs577090562 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897871 | ACCAAAGAAATATTT[C/G]ATGAGCCAATCTCTC | 388795 |
rs577132735 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872866 | GGAGGCCGAGGTGGG[C/T]GGATCGCCTGTGGTC | 388795 |
rs577243799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943311 | GTGAGGTTCAAATGG[A/G]ATAATGTGTACAGAG | 388795 |
rs577266321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942810 | AGTATTCATTTGGGT[A/G]TAAGATAAAAGATAA | 388795 |
rs577267740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873411 | GATTGTGATTATTAA[A/G]AAAAAAGTTGTAGAC | 388795 |
rs577291390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935568 | CTGGAGTGCAATGGC[A/G]CAATTGCAGCTCACC | 388795 |
rs577317643 | snp | C/G | 9.61307e-05 | 0.00693225 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898672 | GGGCTGGAAGGGAGG[C/G]GGGTGGTGAGTGGAC | 388795 |
rs577323517 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864653 | ATGTACGGTCTGTAC[A/G]TGGACTCCACTTCTC | 388795 |
rs577355084 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940952 | ACTCTTACACATTGC[C/T]GGATAGAATGTAGAA | 388795 |
rs577393085 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925976 | TCCCTCGCAGCCACA[C/T]GGCTCTGTCCTGCCT | 388795 |
rs577395073 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913949 | TGACTGGAACCCTAA[G/T]ACTCTGGGCAGCCCT | 388795 |
rs577421598 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921894 | GGCGTGCAGTGTTGC[A/G]ATATCAGCTCACTGC | 388795 |
rs577439976 | in-del | -/GGCT | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909957 | AGGGCTCGCCTCTGA[-/GGCT]GGCTGGCGGGAACAC | 388795 |
rs577441658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879559 | AAGTTTTACATGACA[C/T]GGGAGCCTCTGTAGG | 388795 |
rs577476808 | in-del | -/TAAA | 0.00795532 | 0.062565 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859744 | ATGCCCTTTTACCCC[-/TAAA]TACTTTTCAGTGTAC | 388795 |
rs577531124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901884 | GTAGAGACGGGGTTT[C/T]ACCATGTTGGCCAGG | 388795 |
rs577579403 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868855 | CTGGGCGTGGTGGCA[C/T]GGGCCTCTAATTCCA | 388795 |
rs577581129 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910623 | CCACCACCCTCTCTC[A/G]CTGCCTCAGGGCTCT | 388795 |
rs577617964 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879863 | ATGCTGCGGTGCCCT[A/G]TTTGGGGGTAGCATC | 388795 |
rs577624346 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895044 | TCCATCCTTGCTGTC[G/T]CTTCCCTCCTCCATC | 388795 |
rs577638050 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949608 | CCATACATATATGGA[C/T]ATCTGTTTCTGACAA | 388795 |
rs577648301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885925 | GTCCCTGCCCACCAG[A/G]TTTCCTTCTCTTGCG | 388795 |
rs577680378 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859452 | CCCTCTTGCTTTTGC[C/G]CTTTTCTTTTGGGTG | 388795 |
rs577694165 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896304 | CGCTCAGCTCACCAG[A/G]ACACAGTGAGGTGCC | 388795 |
rs577731141 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880945 | CTCCTGGTTTTTGAA[C/T]ATAGAGAACACAGCT | 388795 |
rs577731764 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878020 | CGCAGTGGCTCACAC[A/C]TTTAATCCTAGAACT | 388795 |
rs577882873 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958714 | AGGCAGCTCTACTCC[A/G]CAGTGGCAGCTATGG | 388795 |
rs577965956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894582 | TAGGGACAAACATGA[C/T]GATGAGGTGGGCCCA | 388795 |
rs577988984 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959203 | CTCAGGGAGGTGGAC[A/C]TGCAAACTCATGGCT | 388795 |
rs578000542 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919986 | CGGGGGCTTGGGAGT[A/G]CCGCTCTTTTATCAT | 388795 |
rs578001086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871397 | TCCTGACTCAGCCTC[C/T]AGAGTAGCTAGGACT | 388795 |
rs578005287 | in-del | -/TCCCTCCC | 0.0219475 | 0.102431 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939015 | CCCTCCTTCCCTCCT[-/TCCCTCCC]TCCCTCCCTCCTTCC | 388795 |
rs578012467 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927261 | GAACTTAGCCTTGAG[A/C]TTCATGAACTTCACG | 388795 |
rs578084100 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913408 | TTTTGTGACCTCATC[A/G]CCTCCCAAGGCCCCA | 388795 |
rs578099174 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899826 | TTATCAGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 388795 |
rs578142185 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948541 | AAGAAAGAAAGAAAG[A/T]AAGAAAGAAAGAAAG | 388795 |
rs578229790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900526 | CCCCCGTGCTCAGCT[A/G]ATTTTTGTATTTTTA | 388795 |
rs578242792 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941679 | CCATATTAAAGTAGA[G/T]TAGTGGTTTCCTGAG | 388795 |
rs578242961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933608 | TTGACCAATAACTTC[C/T]CATTCTCTCTCCCTT | 388795 |
rs745378766 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897398 | GAATGAATGAATGAC[A/G]CACTCAGGGCGGTCT | 388795 |
rs745413936 | in-del | -/TC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939114 | TCCTTCCTTTCTTTC[-/TC]TCTTTCTTTCTCTTT | 388795 |
rs745418154 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869191 | AGAGCTGTTTGCAAG[C/G]CTCAAGCCAACAACA | 388795 |
rs745435854 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884572 | GAGATGGTAATGGCA[A/G]TTGAATTTTCACAGT | 388795 |
rs745542737 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883572 | CTAATTAGATATAGT[A/G]TTCATTCCCATGATA | 388795 |
rs745546685 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935977 | GTCCAAAAGCTTTGT[A/G]TCTTGTCTAAAATCC | 388795 |
rs745550056 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894861 | GATTAAACCACAGCG[C/T]ATCATAAAGCTGACT | 388795 |
rs745592835 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879706 | TGGCGGAAATAGCAA[A/G]GACGTTAGTTCAGAT | 388795 |
rs745609999 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939203 | TTTCTTTCTTTCTTT[-/C]CTCTCTCTCTCTCTC | 388795 |
rs745634578 | in-del | -/TTTG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953808 | TTGTTGATTGTGGTT[-/TTTG]TTTGTTTGTTTGTTT | 388795 |
rs745660844 | snp | C/G | 9.21022e-05 | 0.00678547 | missense | EFCAB8 | GRCh38.p7 | 20:32867660 | CTTAGCCAGGTGCCT[C/G]ACCTCCAGCCTGGGT | 388795 |
rs745686488 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901285 | AGAATTGTCTTGAGT[A/C]ACACATAAAATACAC | 388795 |
rs745717520 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890739 | GGACCTGGGTTCAGG[A/G]CCTGGTCCCACTGCT | 388795 |
rs745737413 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931730 | GCCATTGCATTCCAG[C/T]CTGGGCGACAGAGCA | 388795 |
rs745765397 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862059 | GTGTTTCTCCCTCTT[C/T]CTGTCCTCTAAATGT | 388795 |
rs745778169 | in-del | -/T | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859510 | TTTTCCCATTTGGCG[-/T]TTTACCTCTGTTCAT | 388795 |
rs745840628 | snp | A/T | | | missense | EFCAB8 | GRCh38.p7 | 20:32889308 | CTGGCCAGCTTAACC[A/T]GACCCAGCAGCTCTA | 388795 |
rs745859459 | snp | A/G | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859124 | TCCTGGCTGGCTTTC[A/G]ATGCATGTATCCTTA | 388795 |
rs745878685 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883652 | ACTGTACATTTTGGC[A/G]TGAACACATTGCTTA | 388795 |
rs745911720 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915173 | CTCCCAAAGTACTGG[A/G]TTACAGGCATGTACC | 388795 |
rs745925788 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928929 | CAAATCGTTTTCTGC[A/G]TCAATTAAGATGATC | 388795 |
rs745938297 | snp | C/T | 0.000101859 | 0.00713576 | missense | EFCAB8 | GRCh38.p7 | 20:32959942 | GCCCCCTGGAAGACA[C/T]TGAGGACAGCTGGAA | 388795 |
rs745983631 | snp | A/G | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859682 | TTTTGCCACATTTGT[A/G]TTATTATACATGTTA | 388795 |
rs745989881 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927772 | CATAAAGTGGGGGAA[A/G]TGCTTGCCCTTTGTC | 388795 |
rs745996370 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897754 | TGGGCTTGGTTTTCC[C/G]TCCAGGTCTCACTCA | 388795 |
rs746010816 | snp | C/T | 0.000301477 | 0.0122739 | missense | EFCAB8 | GRCh38.p7 | 20:32959828 | AGCGGCGAGAGCAGG[C/T]GGCGCTGATGGCTCT | 388795 |
rs746112912 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869924 | GTTTTATTGAGTTGA[A/G]TGTTGTAAAGATATC | 388795 |
rs746125332 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933134 | AGGAAGTAATGAAAC[C/T]GAAGAGCTGAGAGAC | 388795 |
rs746173239 | in-del | -/TCC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940047 | CCTTCCTTCCTTCCT[-/TCC]TTCCTTCCTTCCTTC | 388795 |
rs746213038 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866000 | TTAACTGGAGGGACG[A/G]TAGAATGCATAGGAA | 388795 |
rs746237822 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904741 | AGGTGATTCTCCTGC[A/G]TCAGCCTCCTGAGTA | 388795 |
rs746271902 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950992 | GCATGGAAAACAATG[C/T]GCAATATTTATTCAT | 388795 |
rs746283960 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934688 | CCACCATTCTAATGA[C/T]AGTGAATAAGTCTCA | 388795 |
rs746319428 | snp | A/G | 8.89719e-05 | 0.00666919 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878833 | TCTTCCTGGGCCTTG[A/G]TGGGTGGGGTGACTG | 388795 |
rs746338238 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952565 | GCCACTCATACATCT[-/A]ACTCCTGTGAAGTGT | 388795 |
rs746341612 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867162 | TGACCTCAAATGATC[C/T]GCCCTCCTCGGCCTC | 388795 |
rs746382926 | snp | A/G/T | 0.000193428 | 0.00983279 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32918538 | AGTGATGCGGTGCCC[A/G/T]AGAGACAAGGAGCCA | 388795 |
rs746398295 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876187 | CCAGTCGGGGGACTT[A/G]CCTGGTGGAGACGTC | 388795 |
rs746415220 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883081 | GGTGATCCACCTGCC[C/T]TGGCCTCCCAAAGTG | 388795 |
rs746451342 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883266 | GTAGGGGTAGCTTCA[G/T]TTAATGTCCCATAAC | 388795 |
rs746491353 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949646 | AAGGCAATTCAGTGG[A/G]GAAAAGACAGTCTTA | 388795 |
rs746498090 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909566 | AGTTATAAGGTGAAA[G/T]GGACCTTGGACTTGG | 388795 |
rs746659209 | in-del | -/TTT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895314 | TTATTTTATTTAAGA[-/TTT]TTTTTTTTTTTTTTT | 388795 |
rs746675049 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864814 | GATTAAGTTAAGTTA[A/G]ACATGCCTTTGTCTT | 388795 |
rs746684464 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949327 | GAAGACTCTCTGATT[A/C]AGAATAAAATTATCT | 388795 |
rs746698704 | snp | A/C | 8.92339e-05 | 0.006679 | missense | EFCAB8 | GRCh38.p7 | 20:32961228 | GGGCCCAGACCAGCA[A/C]GACCAGCACATCCGC | 388795 |
rs746720010 | in-del | -/TG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951672 | ATACTTCAATAAAAC[-/TG]TTAAAAATAGTCATC | 388795 |
rs746720756 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921048 | ACAAATCATAGTTGA[C/G]TTAGGGTGTGGCTGG | 388795 |
rs746789223 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900123 | TTGGGGAGAGACTGG[A/G]TGAGGCCAGGGTGGG | 388795 |
rs746806058 | snp | C/T | | | missense | EFCAB8 | GRCh38.p7 | 20:32898575 | CAGCCATCGAGAAGT[C/T]CTCTCTGGTGCTGAC | 388795 |
rs746823929 | snp | G/T | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860702 | TTATAAAAATTGGCA[G/T]CATAGTGTGCACCCT | 388795 |
rs746848488 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957853 | TCATCTTAGTTCACC[-/T]TGGCCCTCTTTGCTT | 388795 |
rs746850046 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872437 | CTGGGGCAACAGGCT[C/T]ATGCCTGCCATCCCA | 388795 |
rs746872198 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944605 | TGCCTAGCATCCTTT[A/T]GTTTCAACTTGAAGG | 388795 |
rs746874939 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910840 | CCTTCCGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 388795 |
rs746896702 | snp | A/G | 9.23745e-05 | 0.00679549 | missense | EFCAB8 | GRCh38.p7 | 20:32867595 | AGCTGTCCATCCCAC[A/G]TGGCTTCCAGAACAA | 388795 |
rs746910014 | in-del | -/TTCC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939201 | TCTTTCTTTCTTTCT[-/TTCC]TCTCTCTCTCTCTCT | 388795 |
rs746957133 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956519 | TTGATCTGAAAATAT[A/C]TTTATTTTGCCGTAA | 388795 |
rs746969184 | in-del | -/AT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880900 | CTGTGGGCAAAACAT[-/AT]ATATATATATAAAAC | 388795 |
rs746971998 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884306 | ACAGCCCTAGGAGGT[A/G]CAGGTGCTGTCATCA | 388795 |
rs746974098 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871308 | AGATAGGGTTTTCCT[C/G]TGTAGCCCAGGGTGG | 388795 |
rs746980769 | snp | C/G | 0.000111241 | 0.00745708 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917285 | TCAGCCCTCCTGCCT[C/G]TGGCCATATGCACAG | 388795 |
rs747033724 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897023 | GCTCTCCTGCAGAGA[C/T]GCAGGCTCCTCTGCT | 388795 |
rs747099744 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869017 | CAGCTGGGGCTGTGG[A/T]ATCATCTTGGGGTTG | 388795 |
rs747117941 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935237 | TGGCGTTTTGCTCTT[G/T]TTGCCCGGGCTGGAG | 388795 |
rs747158690 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954531 | TCTTGATTCCTGTAG[C/G]TTTGTAATATGTTTT | 388795 |
rs747160011 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896290 | GGGTGGGGGCACTCC[A/G]CTCAGCTCACCAGGA | 388795 |
rs747174610 | snp | A/G | 9.48362e-05 | 0.00688543 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893335 | GGGGCAGAGGCCTGG[A/G]CATGGCCTAGATGTG | 388795 |
rs747184788 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907735 | AGTCTGGGGCATGGG[A/G]ACAGGGACAGTCTCG | 388795 |
rs747189092 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953674 | CCCATTTTCAAATTG[A/G]GTGTTGTTGTTTTTA | 388795 |
rs747214209 | snp | G/T | | | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32958473 | TGCCTGTGATGGTCC[G/T]CGTGAAAACAGAGCA | 388795 |
rs747217916 | snp | C/T | | | downstream-variant-500B | EFCAB8 | GRCh38.p7 | 20:32962105 | CACCTTGTTCTGTCC[C/T]GTGTGCAGAGAGGGC | 388795 |
rs747314346 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902897 | GTGGTAGCAGGAGCC[A/G]GTGCTGAGTGTGTGG | 388795 |
rs747334964 | snp | C/T | | | missense | EFCAB8 | GRCh38.p7 | 20:32876040 | GTGAAGGCTTTGTCA[C/T]CTGGGTGAGGAGGGT | 388795 |
rs747353844 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916435 | GCTAATTAAAATTTT[C/T]TTTTGTAGAGATGTG | 388795 |
rs747368601 | snp | A/G | 9.27429e-05 | 0.00680903 | splice-acceptor-variant | EFCAB8 | GRCh38.p7 | 20:32898492 | GCTACTGTCTTCCCA[A/G]GCTCTCCATCCCAAC | 388795 |
rs747383819 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887084 | CCACCTGGGGAGCCC[A/G]AGAGCGCAGTCCTCT | 388795 |
rs747415729 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948108 | CTGGGCAGGAAAAAG[A/G]GAGAGAATACACCAA | 388795 |
rs747445951 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915017 | ATCCTCCCACCCCAG[A/C]CTCCAGAGTAGCTAG | 388795 |
rs747458770 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875181 | ACACAGTGCTCCCAT[A/T]TGGCGGGTTTTCAGC | 388795 |
rs747464221 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927616 | TCCCAAAATGCTGGG[A/T]TTAGAGGCGAGAGCC | 388795 |
rs747495981 | in-del | -/CTT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871159 | GCCCGGCCCTCTCTA[-/CTT]CTTCTTTTAAATTTT | 388795 |
rs747536106 | snp | A/C | | | downstream-variant-500B | EFCAB8 | GRCh38.p7 | 20:32962000 | TGGCAAGAGTGAGGA[A/C]CGGCAGCCATCTGGT | 388795 |
rs747554059 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925641 | TACAGGCGTGAGCCA[C/T]GGCGCCCAGCCCCTG | 388795 |
rs747556760 | snp | C/T | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859437 | TTGTCTTGGCCTCTC[C/T]CCTCTTGCTTTTGCC | 388795 |
rs747561210 | in-del | -/AC | 9.127e-05 | 0.00675475 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896572 | ATGGTAATTATCTGT[-/AC]ACACACACACCACTC | 388795 |
rs747576170 | snp | C/T | 8.84056e-05 | 0.00664793 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876067 | GGGTGCCCCTGCTTC[C/T]TCAGGTGCTGGAGGG | 388795 |
rs747583205 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886442 | AGGGCTCTACAGAAA[C/G]GTTGATTGAGAACAC | 388795 |
rs747587336 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941576 | CAACAACATGGATGA[A/G]CCTTGAAAATACTGT | 388795 |
rs747621452 | in-del | -/TT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861919 | TTAACAGAAATGAAC[-/TT]TTAACATTTTACATA | 388795 |
rs747627910 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920363 | GGAGAGGATGGAGAC[A/G]CTCAGGATACTGGAG | 388795 |
rs747652154 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864623 | GAGTCAAATGCAACA[C/T]ACCCGAGCCCCCTGA | 388795 |
rs747660038 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949181 | ATATACTAGCAATGA[A/G]CAGCCAGAAATTGAA | 388795 |
rs747686122 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948994 | GTAGAGGGCAATTAC[A/G]GAAGGAAAAAAAAAG | 388795 |
rs747703671 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907799 | CCTCCAAGAAGTCAG[A/G]GTCTTGGAGGGACTT | 388795 |
rs747713102 | snp | A/G | 0.000184502 | 0.00960296 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32918364 | CTTCTTGGTACAGGT[A/G]CAAGATGTGAACAAC | 388795 |
rs747789040 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914755 | ACTCACCTCCTACCA[A/G]GTCCCTCCCTCAACA | 388795 |
rs747823272 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874940 | TTTTAGTAGAGGCAG[A/G]GTTTTGCCATGTTGG | 388795 |
rs747856492 | snp | A/C | 8.82029e-05 | 0.00664031 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32878802 | TCCCATGACGGTCGT[A/C]CCCCTGTAAGGAGCC | 388795 |
rs747919107 | in-del | -/TCTTTCTTTCTTTCTTTCTTTCTT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939142 | CTTTCTTTCTTTCTT[-/TCTTTCTTTCTTTCTTTCTTTCTT]TCTTTCTTTCTTTCT | 388795 |
rs748020706 | snp | C/T | 9.42818e-05 | 0.00686528 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32960074 | GCAGGTGAGCAAAGT[C/T]TTGGGAGCGGCGTAT | 388795 |
rs748024846 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956238 | GTTTATGTTATTATT[A/G]TATATTTTATTTCTA | 388795 |
rs748026583 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909494 | TCGCCTGGGGCAAGG[A/G]GGAGGCAGGGAGGGC | 388795 |
rs748033877 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954783 | AACGCTTTTTCTGCT[G/T]CTACTGTGATAATCA | 388795 |
rs748057515 | snp | A/G | 9.20853e-05 | 0.00678485 | missense | EFCAB8 | GRCh38.p7 | 20:32911658 | TGAAGATGTGGAACT[A/G]CAACATTGGCAAATG | 388795 |
rs748062752 | snp | C/T | 0.000101384 | 0.00711911 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906799 | CAGTGGGTGAAGGTC[C/T]CCAGTGGAGGCCCCT | 388795 |
rs748068903 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934369 | TGATGGCCCCTTAGG[C/T]TGATTCTATATCTTG | 388795 |
rs748264864 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931635 | GGTGGTGCACTCCTT[A/G]TAATCCCAGCTACTC | 388795 |
rs748277858 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952020 | ATACCAGCACTTTGG[A/G]GGGCCAAAGTGGGTG | 388795 |
rs748293370 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918930 | AGTCACCTGACCTTG[A/G]CCCAGGTGCAGAGGG | 388795 |
rs748297079 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906074 | CCAGATGATGCAGGA[C/G]ACAGCACCCTGCATG | 388795 |
rs748315714 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917818 | CTTTAGTAGATTACT[C/T]GCTCCTTTCCCATTG | 388795 |
rs748370956 | snp | A/G | 9.56251e-05 | 0.006914 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32920215 | TGCCTCGGTGGAGAA[A/G]GTTGGCCGTGATCAG | 388795 |
rs748416869 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915743 | GTGGTGCAGTCTTGG[C/G]TCACTGCAGCCTCCG | 388795 |
rs748431756 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877836 | GAGTTTTATTATCCA[C/T]AGGGGAGAGTGAATA | 388795 |
rs748485441 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958266 | TGAGTACTCAGTGTC[A/G]TGCCTGGTGTATGGT | 388795 |
rs748499161 | in-del | -/A | 9.22424e-05 | 0.00679063 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878698 | TTGTGCTTTCTTTCG[-/A]GGCAGCAAAAGTATG | 388795 |
rs748554681 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960776 | AGGGCCCCCCTGTCT[C/T]GGGCTGGGGAGAGGC | 388795 |
rs748569955 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878892 | GCCCCTCCCTCAATC[C/T]GTGACCTTGCTGGTG | 388795 |
rs748603341 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885777 | AGTCACAGCACCTGG[A/G]TCCTGACTTGGCTTC | 388795 |
rs748623709 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924396 | TTTGTCCATCAAACA[A/G]CCCTGGGAAGTATGT | 388795 |
rs748640886 | in-del | -/CTC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897287 | TCACGAGATCGACAG[-/CTC]CTCAACGGCAGCGGC | 388795 |
rs748647231 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930216 | GCCCTCTAGTAGTTC[A/G]TAGTCGAGTATGACG | 388795 |
rs748711436 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953524 | TTTGTTTGAAACAGC[C/T]ATTCTAATGGGATGA | 388795 |
rs748779530 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901412 | GCTGTCCTGGGTTGT[A/G]TGAGGCCCATGGGCT | 388795 |
rs748798005 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913395 | ATGAGGGCTCCATTT[C/T]TGTGACCTCATCGCC | 388795 |
rs748824258 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862282 | TGTATAGGCATGTGC[C/T]ACCACACCTGGCTAA | 388795 |
rs748875243 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946477 | GTTTCTGGTCCATGT[A/C]CTGTTGTTCAGTCAG | 388795 |
rs748877206 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873479 | AGACCCAGCCAGCAC[A/G]TGGAGAATTTTCTAT | 388795 |
rs748877545 | snp | A/G | 8.8523e-05 | 0.00665234 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32875987 | CAGTGTGTCGGACGA[A/G]ATGCTAAAGGAGCTG | 388795 |
rs748886024 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911784 | TTGACCCTGGGATGC[A/G]CTATTTTTTGTACCT | 388795 |
rs748888557 | in-del | -/G | 9.51792e-05 | 0.00689786 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867559 | AAACGCTCAGTCCCT[-/G]GTTCTTGTTATATTC | 388795 |
rs748910898 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958783 | AAAGGTTGAGCAGTG[A/C]AAGGGGAAAATACAA | 388795 |
rs748968960 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960375 | AGGTCAGTGGTGCAG[C/T]TTTTGTCCTTGAGGA | 388795 |
rs748979464 | snp | A/G | 0.000373308 | 0.013657 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918321 | TGAATTTACCTCTAC[A/G]ACATTGCAGTGCCTT | 388795 |
rs749019599 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882339 | AACCCAGCATTTCCT[C/T]GTTGGTCACTTGATA | 388795 |
rs749020930 | in-del | -/A | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859832 | ACATTAATATGCTAT[-/A]CTAATAATATAGAGT | 388795 |
rs749023704 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869090 | AGAATTCAGTTCCTT[G/T]CCCCTGTGTGACTGA | 388795 |
rs749066656 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921021 | GTGATACTGACTCCC[C/T]GTCCTGAAAATACAA | 388795 |
rs749074140 | snp | A/C | 8.82418e-05 | 0.00664177 | missense | EFCAB8 | GRCh38.p7 | 20:32878789 | TGCACTTCTACCTTC[A/C]CATGACGGTCGTCCC | 388795 |
rs749084622 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908459 | AGGCCGCAGGTGGAG[A/G]GCCAGGGTCTGAATC | 388795 |
rs749087957 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881449 | TGATCCATCCACTTC[A/G]GCCTCCCAAAGTGTT | 388795 |
rs749181865 | snp | G/T | 0.000369617 | 0.0135894 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898635 | CCAGGTAAGAAGTGC[G/T]TCTCTCCTGGCTAAG | 388795 |
rs749241010 | snp | G/T | 9.72053e-05 | 0.00697088 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960031 | AGGGACCCCCAACTC[G/T]CAGCCTTCATTCTTG | 388795 |
rs749265426 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932030 | TGGAGAGGTTGGCAG[C/T]GCTCTGCTTCATTAA | 388795 |
rs749331771 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879385 | ACCGCTCTGCTCACT[C/T]CTCCTCCTCGTGGCT | 388795 |
rs749392154 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916639 | TTCCAAAGGCCACAC[C/T]TTCAGATACTCTCAC | 388795 |
rs749433304 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898383 | GAGAAGGGCATTAGA[C/T]TCCGTGATCTCTGGG | 388795 |
rs749479839 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911966 | ACTTCTCATTCCACA[C/T]ACTGGAGCTTTGGAT | 388795 |
rs749493733 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887569 | GACAGAGCGAGACTC[C/T]GTCTCAATAAAAAGA | 388795 |
rs749534923 | snp | A/C/G | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860699 | CTTTTATAAAAATTG[A/C/G]CATCATAGTGTGCAC | 388795 |
rs749542554 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943478 | GGACCTATGTAAGGT[C/T]GCAAGCAAGTTCATG | 388795 |
rs749565289 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924911 | ACTCCTTGAGGAGCA[-/G]GGTCCCTTCTCTCTG | 388795 |
rs749584281 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924093 | AATCTCAGCTCTCTT[A/G]TCCAGGCTGGAGTGC | 388795 |
rs749586742 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938852 | AGCATATTCCCCAAA[C/T]TGATTTAATGCAATT | 388795 |
rs749603488 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895855 | GGATTACAGGCGTGA[A/G]CCACCGTGCCTGGCC | 388795 |
rs749658534 | snp | A/G | 7.58524e-05 | 0.00615796 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32920194 | GAATATGTTGGTTCA[A/G]TCCAGTGCCTCGGTG | 388795 |
rs749689592 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867475 | GACATCATAACACTA[C/G]TTACCTTGTTCTTTC | 388795 |
rs749734051 | snp | C/G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936082 | CTGTCACCCAGGTTG[C/G/T]AGTGCAGTGGTGCAA | 388795 |
rs749747422 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951737 | TTAATTTGCATTCCT[C/G]TAGTGACTAATGATG | 388795 |
rs749816544 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866192 | TCAATGTGTGTAGAC[G/T]CTGGGCTAATGAATG | 388795 |
rs749852292 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869483 | TCAGGTGATCCGCCT[-/G]CCTTAGCCTCCCAAA | 388795 |
rs749881271 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870809 | ACCCAGCCTCCTATG[A/T]CCTTTGGAAATAAAT | 388795 |
rs749912122 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925092 | CTTACCTGTTGGGTC[G/T]TCCTTCCCATTATTT | 388795 |
rs749925516 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940996 | CGGTGGCTCAGGCCT[A/G]TAATCCCAGCACTTT | 388795 |
rs749932540 | snp | G/T | | | missense | EFCAB8 | GRCh38.p7 | 20:32917505 | CTTGCAGCCCAAGAG[G/T]GTATGTTAACAGGAG | 388795 |
rs749939956 | snp | A/G | 8.92738e-05 | 0.00668049 | missense | EFCAB8 | GRCh38.p7 | 20:32893200 | ACAGAGGTGTGTTCT[A/G]CTATGGAGACGCCAA | 388795 |
rs749970321 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908226 | CTTCAGGAGCCGGCT[A/G]CATCCCCGAGACCCA | 388795 |
rs750004979 | in-del | -/CAAGATCGCA | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949948 | GAGGCTGCAGTGAGC[-/CAAGATCGCA]CCACTGCACTGCAGC | 388795 |
rs750006962 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895817 | CCCAGGTCATCTGCC[C/T]GTCTCGCCCTCCCAA | 388795 |
rs750076571 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913682 | ATTCTGAAGCAAATG[-/C]CCCCTCTAGCTGTGA | 388795 |
rs750103676 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867319 | ATGAGTAAGGTAGGA[C/T]TTGGCTGTATCCTCC | 388795 |
rs750110037 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957743 | TCTAAGCCAAGTCTG[A/T]TTCTCATTCAGCCCG | 388795 |
rs750124213 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951484 | CCTGCATCTATTTAT[A/G]TAAAATTTTAGGAAA | 388795 |
rs750135909 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907029 | CTGACTCCTTCTGTT[A/C]CTCAGGGAAACACAC | 388795 |
rs750151227 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932843 | TGCATTTGCAATTTT[A/G]ATAGCCTTCTTGCAG | 388795 |
rs750177511 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902428 | CTGGGTGACAGAGCA[A/G]GACCCTGTCTTCAAA | 388795 |
rs750186365 | snp | A/G | 9.4594e-05 | 0.00687663 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917518 | AGGGTATGTTAACAG[A/G]AGCACACTCTCCTCC | 388795 |
rs750227470 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914471 | GTCTTTAATGATTGT[A/G]TTAGTTTGTTTTCAC | 388795 |
rs750261559 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946321 | TGGTTCCTTCCCAAT[C/G]TGCTTCACTGAGCCA | 388795 |
rs750290586 | snp | C/T | 0.000108796 | 0.0073747 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918622 | TCACTCTCTAGCCGC[C/T]GGCGTTCACACACCG | 388795 |
rs750297317 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947536 | TGAATTATAAATCAA[A/G]AACAGAAATATCTTT | 388795 |
rs750323293 | snp | C/T | 0.000177117 | 0.00940887 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32878769 | GCGAAAGAGCCAGTA[C/T]CGCCTGCACTTCTAC | 388795 |
rs750323709 | snp | A/T | | | missense | EFCAB8 | GRCh38.p7 | 20:32961539 | TTGTCTCCTCCTTCG[A/T]GCGGCCCCCAAGGCC | 388795 |
rs750357730 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880582 | GGCAATAACTTAAAA[C/G]AAAATTTTGGTTGGG | 388795 |
rs750374685 | in-del | -/G | 0.000191461 | 0.00978232 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960046 | GCAGCCTTCATTCTT[-/G]GGCGTGGCTCCTGCA | 388795 |
rs750393847 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886130 | TGTACCACCTGCAAG[C/G]TCTGTGACCTGGACA | 388795 |
rs750415477 | snp | A/G | 9.3471e-05 | 0.0068357 | missense | EFCAB8 | GRCh38.p7 | 20:32918501 | ATACCAACCTGAGGC[A/G]GAGCCTGGTGTCGGC | 388795 |
rs750438836 | snp | C/T | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859226 | TGCTCTGAATTCTCA[C/T]CCCTGTTCTGGATGG | 388795 |
rs750439389 | snp | C/T | | | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32867647 | ACCATCCATCACCCT[C/T]AGCCAGGTGCCTGAC | 388795 |
rs750459617 | snp | A/G | | | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32911539 | CGTGACGGGCAGGAA[A/G]ACGATGGAGTTTGCT | 388795 |
rs750469755 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944499 | AATAAAGTGACTTAT[A/G]TGCCACTATTACAGT | 388795 |
rs750508861 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922706 | GAGCCTGAAGGAAGC[A/G]AGGAAACATGGCCTG | 388795 |
rs750519204 | snp | A/G | 9.21617e-05 | 0.00678766 | missense | EFCAB8 | GRCh38.p7 | 20:32885549 | TGTTTTTAATCCACC[A/G]GTTCAAGAAGATCGG | 388795 |
rs750527524 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910142 | CTCAGAGCTCCATCC[C/G]TTAGCCATGGGATCG | 388795 |
rs750556110 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884031 | GTGAGCCACTCTGCC[C/T]GGTCAGGTCTTTCTA | 388795 |
rs750593175 | snp | A/G | 9.20598e-05 | 0.00678391 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32906580 | GTCAGTGCTGCGTTT[A/G]AGGAAAGGGATTCTT | 388795 |
rs750685604 | snp | A/G | 0.000101932 | 0.00713831 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960207 | GCTGGGTCAGGGGCC[A/G]GGGGATCCCATGTCC | 388795 |
rs750719280 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898846 | CACAGAGTGATTGGC[A/G]GTCAGTGAAATGTTT | 388795 |
rs750754553 | snp | C/T | 0.00026604 | 0.0115304 | missense | EFCAB8 | GRCh38.p7 | 20:32917438 | TCCTCTTCTGGAACA[C/T]CGGCACACTCAAGCC | 388795 |
rs750784527 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918595 | AGCGAGAGCCCAACC[A/G]GAAGGCTACCCTCAC | 388795 |
rs750793047 | in-del | -/TC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939162 | CTTTCTTTCTTTCTT[-/TC]TTTCTTTCTTTCTTT | 388795 |
rs750846554 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930010 | CACTATAGATATACA[C/T]GAAGGGGAATGAGTT | 388795 |
rs750895362 | snp | A/T | 0.000279603 | 0.0118205 | utr-variant-5-prime | EFCAB8 | GRCh38.p7 | 20:32863792 | TTCTAGGTCAAGGCT[A/T]ATGTCTTCTGAAGAC | 388795 |
rs750960991 | snp | A/C | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860152 | GTTTCTACTAAAAAT[A/C]CGAAAGTTAGCTGGG | 388795 |
rs750966724 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930301 | GGCATCTAGGAAACT[-/G]GGGGACCAGGTGGGT | 388795 |
rs750976591 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942272 | TGCCTTTGTTTATTA[G/T]TGATGTTGACATATT | 388795 |
rs751042279 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936458 | TCAGATCTTATATTT[A/T]AGACTTTAATCCATT | 388795 |
rs751049052 | snp | C/T | 9.44332e-05 | 0.00687078 | missense | EFCAB8 | GRCh38.p7 | 20:32930438 | GCCTGCCGCACACGG[C/T]TGCCCTGCTGAGCAG | 388795 |
rs751063334 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933573 | TTTTTCCTCCTGTCT[C/G]ACCAAAACTTGGTAC | 388795 |
rs751073066 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911439 | CTTGGGAGTGGAGGC[C/T]CCGGCCTCTCCAGCA | 388795 |
rs751075328 | snp | A/T | | | missense | EFCAB8 | GRCh38.p7 | 20:32906974 | AACAACAGCATCCTC[A/T]TCAGTGTCTCCAAGG | 388795 |
rs751123974 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951362 | ATGAAGAATTGATAC[A/G]TTATACAACGTGGTT | 388795 |
rs751135268 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878344 | TGAGCAATAAACTGT[G/T]ATCACACCACTGCAC | 388795 |
rs751142533 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950914 | GCTGGAACTTAAAGT[A/G]GCAGTGTTTGTCCGA | 388795 |
rs751191213 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954485 | CTATTCCATTGGTTT[A/T]TATGTCTGTTTTTAT | 388795 |
rs751219510 | snp | C/T | 0.000153787 | 0.00876755 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893150 | CCAGCCCACACAACC[C/T]CTTCCGTCTCCATCT | 388795 |
rs751238998 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876796 | ACGTGGTAAAACCCT[A/G]TCTCTACAAAAAATA | 388795 |
rs751307341 | snp | A/C | 9.26655e-05 | 0.00680619 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892177 | ACCTCCCAGGCATGG[A/C]TGTGGGCTCTATGTG | 388795 |
rs751313254 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925034 | TGGAAGAGAGGCTTG[A/G]GTGGGCTGGGGTAAG | 388795 |
rs751315061 | in-del | -/AAC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950022 | ACAAAACAACAAAAC[-/AAC]AACAACAACAACAAC | 388795 |
rs751346752 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886024 | GTCCCCACGTCCTAC[C/T]GATTCAGGCCTTTTG | 388795 |
rs751381980 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926139 | ACCTGCTCTCACCGT[A/C]CCAGGGCTGGCAAAG | 388795 |
rs751446353 | snp | A/C/T | 9.42907e-05 | 0.0068656 | missense | EFCAB8 | GRCh38.p7 | 20:32960085 | AAGTCTTGGGAGCGG[A/C/T]GTATAAGCCCAAGGA | 388795 |
rs751560850 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913151 | TGTCTTAGTCCATTC[-/G]GGCTGCTGTAACAGA | 388795 |
rs751577444 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921989 | CATGTGCCACCATGC[C/T]CAGCTGCTTTTTTAT | 388795 |
rs751579210 | snp | C/G | 9.29152e-05 | 0.00681535 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875911 | GGGATGATGCTCTCT[C/G]TTCTCTCTTTGAAGC | 388795 |
rs751593316 | in-del | -/AAA | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948565 | AAGAAAGAAAGAAAG[-/AAA]GAAAGAAAGAAAGAA | 388795 |
rs751615297 | snp | A/C/G | 0.000185567 | 0.00963098 | missense | EFCAB8 | GRCh38.p7 | 20:32918485 | CCCGAGTCTGTGGCC[A/C/G]ATACCAACCTGAGGC | 388795 |
rs751616155 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862281 | GTGTATAGGCATGTG[C/T]CACCACACCTGGCTA | 388795 |
rs751662832 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921000 | TGACCCTGGACACCC[C/T]TCACTGTGATACTGA | 388795 |
rs751679790 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883006 | GGCCTAGTTTTTGTA[C/T]TTTTAATAGAGACGG | 388795 |
rs751683066 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948166 | ACATCATTTCTGATT[C/T]TACAGATATTAAAAG | 388795 |
rs751692972 | in-del | -/TGCC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939986 | AGGCATGAGCCACTG[-/TGCC]TGCCTGCCTGCCTGC | 388795 |
rs751703752 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893375 | GTCATCCTGGTCCCC[A/G]AGCCCCCCACTCCCT | 388795 |
rs751710110 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922430 | CAGGACACAGGCATT[C/T]GCTACATGCCAGCCG | 388795 |
rs751756971 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892426 | AATATCTCCCCACTG[G/T]CTCCAAGGCCCCTGT | 388795 |
rs751758636 | snp | A/G | 0.000102276 | 0.00715034 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32959925 | CCCGTGGGCCGGAGA[A/G]CGCCCCCTGGAAGAC | 388795 |
rs751782808 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863743 | TCCACGTGGTCCTTA[A/C]AACGACTGGAGTTAA | 388795 |
rs751840769 | snp | A/G | 0.000382226 | 0.0138191 | missense | EFCAB8 | GRCh38.p7 | 20:32960129 | ACCAGGTTCCTGTCC[A/G]CCAGGGTGCCATATG | 388795 |
rs751940298 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898037 | GGTTCAAGTTGCCGT[A/G]AAATGCACATTCTCA | 388795 |
rs751949670 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943282 | AGTGAGAATTATATA[C/G]TTCTTATAAGGTTGT | 388795 |
rs752034918 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928668 | TGCAAACTTATAATT[A/T]TACTTCTTTCTTTCC | 388795 |
rs752041765 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955659 | CCCCAAGAAGGGCTT[C/G]AGAAGGGGGCTGGGA | 388795 |
rs752043615 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910105 | AGAAAGCAGCTCTAC[A/C]GATGGGCTGGCGTGG | 388795 |
rs752050638 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957025 | CAGTTCACGAATCCT[A/G]TCCTCTTCTGTATGC | 388795 |
rs752093957 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897562 | ATCCTCCCACCTCAG[A/G]CCCCCGAGTAGCTGG | 388795 |
rs752112714 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880185 | CCAGGCCACGGGGAA[A/G]TCAAAGAGCTGGAAG | 388795 |
rs752128686 | in-del | -/TTC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935185 | CTTTTCTTTCTTTCT[-/TTC]TTCTTTCTTTTTTTT | 388795 |
rs752136042 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904149 | GCAGGTGCACCACCA[G/T]GCCCAGCTAATTTTT | 388795 |
rs752189035 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888190 | CACCTCAGCCTCCCA[A/G]GTAGCTGGGACTACA | 388795 |
rs752298671 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875833 | GTCTTCAGTGTGTCC[C/T]CCTCAGCACCCAGAC | 388795 |
rs752315779 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898007 | CAGCCCCTTCGACTG[C/T]GCGTCATCTTTTGTG | 388795 |
rs752353783 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928625 | GTGTGGGAGCTTTAG[C/T]GTTTTCTACATATAA | 388795 |
rs752358114 | snp | A/G | 9.52064e-05 | 0.00689885 | missense | EFCAB8 | GRCh38.p7 | 20:32930432 | GGCCTCGCCTGCCGC[A/G]CACGGCTGCCCTGCT | 388795 |
rs752413347 | snp | A/C/T | 9.20938e-05 | 0.00678516 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920063 | GGTGACTTGGGTGCC[A/C/T]ATCTTTCTTTCCAGA | 388795 |
rs752418377 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887062 | TCCATTGTCTTCACC[A/G]CCAGAACCACCTGGG | 388795 |
rs752458264 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955147 | GCTTAAGGCAGGCCC[C/T]TCCCTCCCCCTAAAG | 388795 |
rs752484115 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884147 | TTTGTTCAACCTACA[A/G]ACCCGGAGAGCATTT | 388795 |
rs752484530 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895478 | CACAGGCACGCCACC[A/G]CCACTTCTGGCTAAT | 388795 |
rs752491206 | in-del | -/TG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924822 | TGGCTGGCAGGGCTG[-/TG]TGTGTGTGTGTGTCC | 388795 |
rs752503921 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936325 | ACGTGTGAGCCACCG[C/T]GCCTGGCCTATTTTT | 388795 |
rs752599817 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890953 | CTAAATTGTGTGATA[-/C]AGAGAAAGTGGTCAG | 388795 |
rs752607306 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922598 | AGAAAGCCGGGAAGA[A/T]GGCAGGGAGAACAGA | 388795 |
rs752656858 | in-del | -/GTGTG/GTGTGTG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921393 | GTGTGTGTGTGTGTT[-/GTGTG/GTGTGTG]TTTGTAGAGATGGGG | 388795 |
rs752660366 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950663 | CTGCAGGCAAATCCC[C/G]CGGGTTGCTTTTAGC | 388795 |
rs752689091 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865532 | GCCAGGCGCAGTGGC[C/T]CATATCTGTAATCCC | 388795 |
rs752721057 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905343 | CAAAGAGACAGGGAC[A/G]CCTGTGTAGTTTCAT | 388795 |
rs752753932 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920005 | CTCTTTTATCATCTT[C/T]CTCTGGTCTCTGGTC | 388795 |
rs752810747 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902533 | AGGAGGATCCCTTGA[-/G]GCCAGGAGTTCAAGA | 388795 |
rs752821941 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892339 | ATGAACCAGGAGGCC[C/T]AGGCCTCCTGCAGCA | 388795 |
rs752873262 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891454 | ATCTCCTGACCTCAG[G/T]TGATCCACCTGCCTC | 388795 |
rs752896348 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946251 | GCCCTCTGAAAAGTC[A/T]GCATGTTGGATGTAC | 388795 |
rs752910798 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947213 | TACCTTTGTGTCTTC[A/G]TCAACATTTGGTGTT | 388795 |
rs752921750 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874345 | CTCCCACCTCAGTCT[C/G]TCGACCAGCTGGGAC | 388795 |
rs752926221 | snp | C/T | 9.56069e-05 | 0.00691334 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875876 | CGTGGCAGTGATGGG[C/T]CGAGGGACTTGTGAG | 388795 |
rs752948849 | in-del | -/AG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947797 | ATTAAGAAACTAGAA[-/AG]AGGTCTGGTGCGGTG | 388795 |
rs752996097 | snp | C/T | | | missense | EFCAB8 | GRCh38.p7 | 20:32961299 | GGGAGCAGGCTGTGC[C/T]GGATACCACGGACAG | 388795 |
rs753008058 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935231 | TTGAGATGGCGTTTT[G/T]CTCTTGTTGCCCGGG | 388795 |
rs753039647 | in-del | -/TTTTTTTTTTTTT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935193 | TTCTTTCTTTCTTTC[-/TTTTTTTTTTTTT]TTTTTTTTTTTTGAG | 388795 |
rs753040397 | snp | C/T | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859367 | ATTCTAAATATCAAC[C/T]GAGTTTTACATCTCA | 388795 |
rs753060587 | snp | A/C | 0.00014951 | 0.00864481 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931355 | GGAGGATTACTGGAG[A/C]GTTGCTCAGGAAAGT | 388795 |
rs753072910 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908994 | TCCTGTGGAGGATGG[G/T]GGTAAGGGGGCCCAC | 388795 |
rs753076276 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954312 | ATTTTTGTATATGGC[A/C]TAAAATAACAGTCCA | 388795 |
rs753081548 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927420 | CGTGATCTTGGTTCA[C/T]TGCAACCTCCGCCTC | 388795 |
rs753083750 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942908 | CCACTCTTACTATAT[A/G]CCAGTTTTACATACA | 388795 |
rs753084509 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870544 | CGCTTGGTTGCCCAG[G/T]CTGGAGTGGAGTGGT | 388795 |
rs753108604 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869700 | GGAGGCACACAGTAT[A/G]GGGGCTGCTTAAGTC | 388795 |
rs753160357 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955607 | TCAGTATTCGAGAGT[C/G]CTGTTTGGATTAGTA | 388795 |
rs753160818 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920886 | GGCATCTCCAGACTC[C/T]AGTTAGAATGCCCTC | 388795 |
rs753163015 | snp | A/G | | | missense | EFCAB8 | GRCh38.p7 | 20:32908282 | TCCCCCAGAATATTC[A/G]CGTGTGGGACATGCT | 388795 |
rs753171689 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941235 | CCAGTCTGGGCAACA[A/G]GAGCAAAACTCCAAA | 388795 |
rs753218371 | snp | A/G | 0.000102454 | 0.00715656 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32959913 | GGCCCTGATGTCCCC[A/G]TGGGCCGGAGAGCGC | 388795 |
rs753287423 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875133 | GAGTTGGTCTTTTTT[A/T]GTGCCTCCCCTCCCC | 388795 |
rs753330998 | snp | C/T | 9.23148e-05 | 0.0067933 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906541 | CCCGGCCCTGCAGCC[C/T]TCACTCCTTTGATAT | 388795 |
rs753335878 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897354 | GTACCCTGCGCTTGG[A/T]GGGCTCCCAATACAT | 388795 |
rs753358179 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926291 | ATTGGAATGTGCTTA[C/T]GACAAAATTTAAAGC | 388795 |
rs753366985 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928457 | GACCAGGCTGGTCTC[A/G]AACTCTTGACCTCAT | 388795 |
rs753374654 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941160 | GGGAGGCTGAGGCAG[C/G]AGAATCGCTTGAACC | 388795 |
rs753386960 | snp | G/T | 9.40601e-05 | 0.0068572 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32918511 | GAGGCGGAGCCTGGT[G/T]TCGGCTCCCCCAGTG | 388795 |
rs753393974 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886972 | TAGTGCAAGGGTTGG[A/G]AGTTACCAAGCTACT | 388795 |
rs753443700 | snp | C/T | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859306 | GTCAACTTTAGGGAA[C/T]AGATTGAGGCAGATG | 388795 |
rs753444880 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886174 | TCCCTGTGCCTCAGT[C/T]TTCCCATCTGTCAAA | 388795 |
rs753472880 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917664 | GTAGGTGGTAGTTTC[G/T]GTAATTATCCTCATT | 388795 |
rs753474826 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908835 | ACAGGGGCCACGTCC[A/G]AGCAGCATCTCTGCA | 388795 |
rs753642987 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950095 | CTTCCAGAAGAAATC[A/G]TAGGAGAAAACCTTT | 388795 |
rs753721794 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908893 | CAGATAGGAAGGCCA[C/T]CTGTGACTCAGGACT | 388795 |
rs753767281 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864462 | TGGCACATGCCTGTG[A/G]TCCCCGCTACTCCAG | 388795 |
rs753837478 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948452 | CAGAAAGTTGAAAAG[C/G]GTACAATACTTCCCA | 388795 |
rs753858582 | snp | C/T | 9.23745e-05 | 0.00679549 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32885589 | GACTGTCACCAAAGA[C/T]GGGATCCTGCAGTTC | 388795 |
rs753886334 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931059 | GTATCTCAGAGATGT[A/G]AGTAAGAACTGCCCC | 388795 |
rs753887174 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889943 | GAGGTGGAGGTTGCA[A/G]TAAGCTGAGATCGCG | 388795 |
rs753936089 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861869 | TGTTTCCAGGCTCTT[C/T]TTTATGCATGTGCCA | 388795 |
rs753964112 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901001 | GCCACCGCGCCCGGC[C/T]GTCCAGTGCCTTTTT | 388795 |
rs753977179 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945823 | TTTCACCAGACTTAC[A/G]CATGTAAATTCGCAA | 388795 |
rs753982480 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899832 | GCCCGCCTCGGCCTC[C/G]CAAAGTGCTGGGATT | 388795 |
rs754001869 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944564 | TTTATCAGAAAGCTT[G/T]GTATTTTCATATGCT | 388795 |
rs754017409 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872362 | GTGCCATCACCGGCA[C/T]ATCTCAGTGCCCACA | 388795 |
rs754022404 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935189 | TTCTTTCTTTCTTTC[-/T]TTCTTTTTTTTTTTT | 388795 |
rs754024950 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959690 | GGAAAGGATCAGGCC[A/G]GGAAGGGGAGAGGCT | 388795 |
rs754073281 | snp | A/G | | | missense | EFCAB8 | GRCh38.p7 | 20:32911576 | GGGGGCCAGCACGTG[A/G]AGATGACCGCCATGG | 388795 |
rs754075484 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885206 | TCCTCTGTCCCATCA[C/T]GTCGCGAGGAGGCTG | 388795 |
rs754105798 | in-del | -/TTTTTTTTTTTTT | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860496 | TGATGGTGGTAACTT[-/TTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 388795 |
rs754112625 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903857 | ACTTGGGGCCAGGCT[A/G]GATAATGGGAGCCAC | 388795 |
rs754135756 | snp | A/G | 9.48092e-05 | 0.00688445 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863843 | CCAAAAGGTAAGAAA[A/G]ACAATTATCTGAACT | 388795 |
rs754163785 | in-del | -/TCTC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939112 | CTTCCTTCCTTTCTT[-/TCTC]TCTTTCTTTCTCTTT | 388795 |
rs754166862 | snp | C/G | 9.22552e-05 | 0.0067911 | missense | EFCAB8 | GRCh38.p7 | 20:32911631 | TGCTCACAGGTTTGC[C/G]GGATGGCACAATGAA | 388795 |
rs754186013 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868808 | TGGCCAACATGGTGA[A/G]ACCCCGTCTCTACTA | 388795 |
rs754198747 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938336 | GCCATTTATGAAAAC[C/T]CACAGGTAGCATAAA | 388795 |
rs754237800 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919738 | TCCTGGCCTGAAATT[A/G]TCTGCCCGCCTCAGC | 388795 |
rs754281455 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945267 | AGCCTCAAGTGATCT[A/T]CCCACAGCCTCCTGA | 388795 |
rs754294494 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932489 | CTTACAGCGAAGAGT[C/G]TAAGTCCCATTCCTG | 388795 |
rs754303083 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958051 | TCCTTCCCCCACCAC[A/C]CCAAATCTCATATCT | 388795 |
rs754314009 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953125 | ATGCCCTCAATATTT[A/G]TTAATATTGTAACAT | 388795 |
rs754323964 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891326 | TGGTCTGCTGGGCCC[A/G]TGTTTGTTGGCTCAT | 388795 |
rs754327680 | snp | C/T | 9.47643e-05 | 0.00688282 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32931264 | CTCTGAAGCACACAA[C/T]AAGTTCCGGTTGTTA | 388795 |
rs754407293 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959562 | AGAGGACAGAGTGGT[A/G]GGAGAGTGGCAGGAC | 388795 |
rs754460445 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947745 | AAATGCCTATATTAG[A/G]AGGAAAAAAGTTCAA | 388795 |
rs754507801 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930191 | TGAACAAAAAAGACG[C/T]AAAATCCCTGCCCTC | 388795 |
rs754531260 | in-del | -/TAT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915381 | ACACTAGAACACAAA[-/TAT]AATTCAGCAAGTTCT | 388795 |
rs754559825 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914685 | AATCATCAGGTCTTG[C/T]GAGAACTCACTCACT | 388795 |
rs754593630 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925330 | GTTCAAGTGATTCTC[A/G]TGCCTCAACCTCCTG | 388795 |
rs754629576 | snp | A/G | | | utr-variant-3-prime | EFCAB8 | GRCh38.p7 | 20:32961646 | GTCCTCCAGCAGGGC[A/G]ACCAGGCCCATGGCG | 388795 |
rs754684580 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32907722 | GATGAAGGGTCTGAG[A/T]CTGGGGCATGGGGAC | 388795 |
rs754708618 | in-del | -/AAGAAAAAGAGTT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931761 | GACTTCGTTTCAAAA[-/AAGAAAAAGAGTT]AAGAAAAAGAGTTAG | 388795 |
rs754753187 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954865 | TTTGAAAATTCAACC[-/T]TGCATTCCTGGAGTA | 388795 |
rs754762355 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883116 | TATTACAGGTGTGAG[A/T]CATTGCGCCTGGCCA | 388795 |
rs754772765 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959458 | AAGGCAAAGGCAGGG[-/T]TTCCCTGGGGCAGGG | 388795 |
rs754779034 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893547 | GAGGCTGTGCGGGTG[C/T]GGTCTGGGGGTGCAG | 388795 |
rs754800072 | snp | G/T | 0.000276332 | 0.0117512 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920055 | ACCCTCATGGTGACT[G/T]GGGTGCCCATCTTTC | 388795 |
rs754813041 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891852 | TTTTTTAATTGAGAC[A/G]GGGTCTTGCTCTGTC | 388795 |
rs754846499 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903916 | CTGGCTTAGGCCCCC[C/T]GGGAGTGGTGGAGGA | 388795 |
rs754875751 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949106 | TACTAAAAAGAGTTA[A/G]TAAGGAGTTTAACAA | 388795 |
rs754898164 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915877 | AGGGTTTCATCATGT[C/T]GGCCAGGCTGGTCTT | 388795 |
rs754933633 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902782 | TGGAGTCAGCCTCAG[C/T]CTCCAAGGCAGTGTG | 388795 |
rs754941879 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920532 | TGGCGGGAGGCTAAA[G/T]GTGCTTCTTACATGG | 388795 |
rs754951031 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934317 | AATAGTATTCCATTA[A/T]GTATATACACCACAT | 388795 |
rs755011178 | snp | A/G | | | missense | EFCAB8 | GRCh38.p7 | 20:32931302 | AGCAACTTGGGACCA[A/G]CTTCCCACACTACAT | 388795 |
rs755045278 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891364 | CTGGGATTACAGGTG[C/T]GCGCTACCACACCCA | 388795 |
rs755045800 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881260 | GGAATGCAGTGGTGC[A/G]GTCTTAGCTCACTGC | 388795 |
rs755073184 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861885 | TTTATGCATGTGCCA[A/G]TATGCACATGCATAT | 388795 |
rs755128224 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872992 | AGCTACTTGGGAGGC[C/T]GAGGCAGGGAGAATT | 388795 |
rs755185994 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899918 | ACTGTGCCGTTTACT[A/G]TGGATAAACTGGTAG | 388795 |
rs755220209 | snp | C/T | | | missense | EFCAB8 | GRCh38.p7 | 20:32959815 | GCCCTGATATACCAG[C/T]GGCGAGAGCAGGCGG | 388795 |
rs755251588 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943232 | TAGGCTAGTTATTGA[A/G]CATGTCTGACTCTCA | 388795 |
rs755273794 | snp | C/T | | | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32911614 | TGAGTCAGAGCGGTG[C/T]CTGCTCACAGGTTTG | 388795 |
rs755277723 | snp | A/G | 0.000180018 | 0.0094856 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912905 | TAGGTTCCAGTAGCT[A/G]CGTGTTCTCTCTCCA | 388795 |
rs755280816 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869590 | GCACATAGTCCTGCA[C/T]ACCCTGTCACCTGTG | 388795 |
rs755345679 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938477 | AATGAAATAAAAAGT[A/G]TCTATATTGGGGAGG | 388795 |
rs755371621 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872860 | ATTTTGGGAGGCCGA[G/T]GTGGGCGGATCGCCT | 388795 |
rs755493392 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918784 | AGCTGGGGCTAGGTC[C/G]CTTTCCAGGGCATGG | 388795 |
rs755518062 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893374 | GGTCATCCTGGTCCC[C/T]GAGCCCCCCACTCCC | 388795 |
rs755520131 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953236 | TGTTAATGGACACTT[C/T]AGTTGACTCCACCTC | 388795 |
rs755595978 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960318 | ATGGACAGGTCTGGG[A/G]TGAGACTAATGTGGC | 388795 |
rs755618162 | in-del | -/TT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904604 | ACACCTGAATGGAGC[-/TT]TTTTTTTTTTTTTTT | 388795 |
rs755746462 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924002 | TCAGTGGTAGCTAGT[A/C]ATTATTGAGCTCTCA | 388795 |
rs755857401 | snp | A/T | 8.9218e-05 | 0.0066784 | missense | EFCAB8 | GRCh38.p7 | 20:32875977 | AGGTTCTGAGCAGTG[A/T]GTCGGACGAGATGCT | 388795 |
rs755878174 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891583 | CAGCTGTCATCTGCT[C/T]GGAGGTACTCAGACA | 388795 |
rs755928567 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932852 | AATTTTGATAGCCTT[C/G]TTGCAGTCTTATGTG | 388795 |
rs755930572 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948705 | TTACCCCAGATATAC[A/G]AGGTTGGTTTAATAT | 388795 |
rs755935919 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901295 | TGAGTCACACATAAA[A/G]TACACTGACACTAAC | 388795 |
rs755967959 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862968 | CCCTTCATTTTGTTC[A/G]GACTGTCTGGCCAGG | 388795 |
rs755990841 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902465 | AAAAGACTCCATTCA[A/G]GTCAGACACGGTGGC | 388795 |
rs756053767 | snp | C/T | 8.84995e-05 | 0.00665146 | missense | EFCAB8 | GRCh38.p7 | 20:32878770 | CGAAAGAGCCAGTAC[C/T]GCCTGCACTTCTACC | 388795 |
rs756095183 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947685 | ACATTTCAAAATTTA[C/T]GAGATGCCACAAAAA | 388795 |
rs756145547 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944502 | AAAGTGACTTATGTG[C/T]CACTATTACAGTATT | 388795 |
rs756147338 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899011 | TAACTGGCAGCATTG[G/T]TTCTTTGCAGATGGT | 388795 |
rs756188859 | in-del | -/AGACCAGCA | 8.87351e-05 | 0.00666031 | cds-indel | EFCAB8 | GRCh38.p7 | 20:32961218 | GACCAGCAGGGGCCC[-/AGACCAGCA]AGACCAGCAAGACCA | 388795 |
rs756193551 | in-del | -/TTTTTTTTTTTTTT | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860495 | CTGATGGTGGTAACT[-/TTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 388795 |
rs756195164 | snp | C/T | 9.11535e-05 | 0.00675044 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32961086 | TTGATCCTGGGTGTC[C/T]CCGGCTCCAACTGGT | 388795 |
rs756267770 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884032 | TGAGCCACTCTGCCC[A/G]GTCAGGTCTTTCTAT | 388795 |
rs756306374 | snp | C/T | 9.21277e-05 | 0.00678641 | splice-donor-variant | EFCAB8 | GRCh38.p7 | 20:32906631 | CAGGAACTTCCTGGG[C/T]AAGTCACCTTCATGT | 388795 |
rs756326135 | snp | C/T | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860679 | GCCCAGGCTATTTTT[C/T]CATTCTTTTATAAAA | 388795 |
rs756334475 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871058 | GGGTTTCACCATGTT[A/G]GTCAGGCTAGTCTTG | 388795 |
rs756380693 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901362 | CTCATAATGTTATAA[A/G]AAAGTTTATGAATTT | 388795 |
rs756384301 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867390 | TTCCCTCTCCAAAGT[C/T]GGAAGAGTCTAGGTT | 388795 |
rs756388220 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951502 | AAATTTTAGGAAATG[A/C]AAACAAATGTGTAGT | 388795 |
rs756402645 | in-del | -/ACA | | | cds-indel | EFCAB8 | GRCh38.p7 | 20:32931260 | TTGTCTCTGAAGCAC[-/ACA]ACAAGTTCCGGTTGT | 388795 |
rs756427293 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942302 | TTTCTTAATCTATTG[A/G]CTTTGTATAACTTTA | 388795 |
rs756520526 | in-del | -/TGTG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924820 | TGTGGCTGGCAGGGC[-/TGTG]TGTGTGTGTGTGTCC | 388795 |
rs756522913 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941258 | CTCCAAACTCTGTTT[-/A]AAAAAAAAAAAAAGA | 388795 |
rs756550447 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893776 | GCCTGGCTGGCATGG[A/G]TGAGTGGGCACAGCT | 388795 |
rs756599281 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877540 | ATGTTCTATAATAAA[C/T]ATTTCCTTTAGAACA | 388795 |
rs756622726 | snp | A/G | 0.000184128 | 0.00959324 | missense | EFCAB8 | GRCh38.p7 | 20:32920138 | CACAGCAAACAGTCC[A/G]TTTACAAAGAGGATG | 388795 |
rs756628889 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889875 | GGAGTGGTGGCACAC[A/G]CCTGTAATCCCAGCT | 388795 |
rs756656140 | snp | C/G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930024 | ATGAAGGGGAATGAG[C/G/T]TCCTTCCCCACATCA | 388795 |
rs756678680 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899748 | CTCGGCTAATTTTGT[A/G]TTTTTAGTAGAGACG | 388795 |
rs756712094 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936621 | AAATCAATTGACTAT[C/T]AGTGCATGGGTTTAT | 388795 |
rs756752472 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884342 | GTGAGGAAACCAAGT[C/T]CTCCCTGAGATGGCC | 388795 |
rs756779908 | snp | C/T | 9.23318e-05 | 0.00679392 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892199 | CTCTATGTGGCCTTC[C/T]GTCTTTCCCCCAGAT | 388795 |
rs756782372 | snp | G/T | 9.3541e-05 | 0.00683826 | missense | EFCAB8 | GRCh38.p7 | 20:32930444 | CGCACACGGCTGCCC[G/T]GCTGAGCAGCTGCAT | 388795 |
rs756806079 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894764 | GAACGTTAGGCACCT[A/C]GTAAGTGCACAGTGA | 388795 |
rs756823050 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870697 | GGTAGAGATGGGGTC[G/T]TGCTATGTTGCCCAG | 388795 |
rs756829329 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865961 | AGAGGAGGCTTATAT[G/T]TAGGAGATGGATCCC | 388795 |
rs756882077 | snp | G/T | | | missense | EFCAB8 | GRCh38.p7 | 20:32906980 | AGCATCCTCATCAGT[G/T]TCTCCAAGGACAAGG | 388795 |
rs756916270 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951420 | GAGAAGCCAGACGAA[A/C]ACCTGTACATATTGT | 388795 |
rs757030883 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946264 | TCTGCATGTTGGATG[C/T]ACATCTCAGTCTTTC | 388795 |
rs757123407 | snp | A/G | | | missense | EFCAB8 | GRCh38.p7 | 20:32912800 | CTTCAACAGATTAGT[A/G]GGATTATCCATATGA | 388795 |
rs757130907 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877208 | TTATTTATTTCTTTC[-/T]TTTTTTTTTTTTTTT | 388795 |
rs757130942 | in-del | -/AA | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903784 | GGAGGCTGATACGGC[-/AA]AGTCAGGGGCCTGGG | 388795 |
rs757167422 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900131 | AGACTGGGTGAGGCC[A/C]GGGTGGGGTTGGGGC | 388795 |
rs757207982 | snp | A/G | 9.18991e-05 | 0.00677799 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32917502 | GCCCTTGCAGCCCAA[A/G]AGGGTATGTTAACAG | 388795 |
rs757227013 | snp | C/T | | | stop-gained | EFCAB8 | GRCh38.p7 | 20:32960108 | CCCAAGGAACGCTTG[C/T]AGAATACCAGGTTCC | 388795 |
rs757227737 | snp | A/G | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859474 | TTTTGGGTGGTCTCT[A/G]TTGGCAGCAACCAGC | 388795 |
rs757239703 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904512 | CTGTGTTGCCCAGGC[-/T]GGTCTTGAACTCCTG | 388795 |
rs757262883 | snp | C/T | 8.90512e-05 | 0.00667215 | missense | EFCAB8 | GRCh38.p7 | 20:32878753 | AGGGAAAAGAGGACA[C/T]GCGAAAGAGCCAGTA | 388795 |
rs757283467 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955694 | TCCCCACCTCCAAAC[A/G]GCAAGCATATATCTT | 388795 |
rs757303547 | in-del | -/AG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948571 | GAAAGAAAGAAAGAA[-/AG]AAAGAAAGAAAAGAA | 388795 |
rs757357505 | in-del | -/A | | | utr-variant-5-prime | EFCAB8 | GRCh38.p7 | 20:32863791 | TTCTAGGTCAAGGCT[-/A]AATGTCTTCTGAAGA | 388795 |
rs757404664 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893409 | TCTGCTCTGGAGTCT[C/G]TGGGAAGGCGTCTGC | 388795 |
rs757414588 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883019 | TATTTTTAATAGAGA[C/T]GGGATTTCACCGTAT | 388795 |
rs757425551 | snp | C/T | 9.23574e-05 | 0.00679486 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875918 | TGCTCTCTGTTCTCT[C/T]TTTGAAGCCCTGGGC | 388795 |
rs757461144 | in-del | -/CCTTCCTTCCTT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940024 | CTCCCTCCCTCCCTC[-/CCTTCCTTCCTT]CCTTCCTTCCTTCCT | 388795 |
rs757480068 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869827 | GAATTTTCCATATTG[C/T]TACATAATCTTCCAA | 388795 |
rs757490111 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876431 | GTGGCTGTTACATCT[A/G]AAAGTGTCAGGCTTT | 388795 |
rs757516947 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877073 | TCAGACTCATCAGCA[C/T]TGGAGCCAGTATTCA | 388795 |
rs757533426 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881954 | GGCTCACACCTGTAA[C/T]CCCAGCACTTTGGGA | 388795 |
rs757599360 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929950 | CTTGAACAAGAATTT[G/T]TTTAAAATGCTTTCT | 388795 |
rs757625119 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888591 | GAACTCCTGGGCTCA[A/G]GTGATCCTCCCACCT | 388795 |
rs757735658 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916447 | TTTTTTTTGTAGAGA[C/T]GTGGTCTTGCTCTGT | 388795 |
rs757751108 | snp | A/G | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860410 | TTTTTTGGCAATAAT[A/G]CTACTGAAGCATTGT | 388795 |
rs757783852 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943303 | ATAAGGTTGTGAGGT[G/T]CAAATGGAATAATGT | 388795 |
rs757792548 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909613 | AACACTAGGGTTTGG[A/G]AGGCTCAGTCTCGGG | 388795 |
rs757804654 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897569 | CACCTCAGGCCCCCG[A/T]GTAGCTGGGAATACA | 388795 |
rs757810276 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910116 | CTACAGATGGGCTGG[C/T]GTGGGATCAGCTCAG | 388795 |
rs757890461 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909416 | AAAACAGATAATTTC[G/T]GTAGAAAGTGCTATG | 388795 |
rs757915907 | snp | A/T | 9.20938e-05 | 0.00678516 | missense | EFCAB8 | GRCh38.p7 | 20:32920084 | TCTTTCCAGAAACCT[A/T]CCAGTGCTTCTGGCA | 388795 |
rs757927779 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865706 | TGGGAAGCTGGTTCA[C/G]GAGAATCACTTGAAC | 388795 |
rs758013550 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949192 | ATGAACAGCCAGAAA[C/T]TGAAGTAAAAGATAC | 388795 |
rs758047602 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888326 | TGCCTCCCGGGTTCA[G/T]GTGATTCTTCTGCCT | 388795 |
rs758056723 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865486 | GTGTCAGAAGCAGGG[C/T]AAAGTCATTGATCAG | 388795 |
rs758067852 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915970 | AGCCACCCTGCCCAG[C/T]TGCTGTTACCTAGTT | 388795 |
rs758082123 | snp | C/T | 9.36812e-05 | 0.00684338 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885653 | AGGGTGAGTGGGGCC[C/T]CTACACATGGTGCAC | 388795 |
rs758146944 | snp | C/T | 9.49803e-05 | 0.00689066 | missense | EFCAB8 | GRCh38.p7 | 20:32930435 | CTCGCCTGCCGCACA[C/T]GGCTGCCCTGCTGAG | 388795 |
rs758166049 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872397 | CCCTCAGGGGACCAA[C/T]GTTTGTTGAAGCCAG | 388795 |
rs758171731 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951499 | ATAAAATTTTAGGAA[A/T]TGCAAACAAATGTGT | 388795 |
rs758195219 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884237 | AAAACATTGGCTTAC[C/T]TTTACTGAGCCTGGG | 388795 |
rs758233028 | in-del | -/TT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870861 | TCTACTTCTTCTTCT[-/TT]TTTTTTTTTTTCCTG | 388795 |
rs758250826 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868603 | GCTTAAACCAATGCA[C/T]GTTTATCACCTCACA | 388795 |
rs758251735 | snp | C/T | 0.000184111 | 0.00959279 | missense | EFCAB8 | GRCh38.p7 | 20:32911664 | TGTGGAACTACAACA[C/T]TGGCAAATGCCTGTT | 388795 |
rs758255522 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922692 | GTGGCATCTGCATAG[A/G]GCCTGAAGGAAGCGA | 388795 |
rs758257977 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923813 | CACATCATGTCCTGG[A/G]TACACTGCACAGAGT | 388795 |
rs758323173 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902064 | AAAAATAGATAAAAT[-/G]GTATAATTCTTCCAT | 388795 |
rs758360679 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899786 | TCTGTGTTGGTCAGG[C/T]TGGTCTCGAACTCCT | 388795 |
rs758389369 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925843 | ACTATCTGGGATTCC[G/T]GGGCTGAGTGAGACT | 388795 |
rs758502674 | snp | A/G | 9.68289e-05 | 0.00695737 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867548 | TCAGGAAATTGAAAC[A/G]CTCAGTCCCTGGTTC | 388795 |
rs758538296 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932657 | TCTTGCTTTTCTTGC[G/T]GTATGATATATCTTG | 388795 |
rs758558423 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947413 | ACATTATTTTTAAGT[G/T]CACACAGAACATTAA | 388795 |
rs758633306 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935232 | TGAGATGGCGTTTTG[C/T]TCTTGTTGCCCGGGC | 388795 |
rs758634947 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895851 | GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCT | 388795 |
rs758650826 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862737 | GGTTCAAGCAATCCT[C/T]CTGCCTCAGCCTCCC | 388795 |
rs758681803 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891457 | TCCTGACCTCAGGTG[A/T]TCCACCTGCCTCAGC | 388795 |
rs758708021 | snp | C/G | | | utr-variant-3-prime | EFCAB8 | GRCh38.p7 | 20:32961836 | CTGTGGGCATCCACA[C/G]GTGATGAGGTTGGGC | 388795 |
rs758719928 | snp | A/G | 9.28376e-05 | 0.0068125 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32893294 | CCCCAGGGCCTCCAA[A/G]TGGGGTAGCTAAGAT | 388795 |
rs758800309 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927470 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAA | 388795 |
rs758836396 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909001 | GAGGATGGGGGTAAG[A/G]GGGCCCACAAGAAGG | 388795 |
rs758851919 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896580 | TTATCTGTACACACA[C/T]ACCACTCAAAATAAA | 388795 |
rs758857946 | snp | C/T | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859427 | GGAATGGTACTTGTC[C/T]TGGCCTCTCCCCTCT | 388795 |
rs758909400 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869713 | ATGGGGGCTGCTTAA[A/G]TCTCTCTACTGCAGA | 388795 |
rs758939321 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896894 | TCACCCCGGTAGCTT[C/T]TCATCACATTTGGAA | 388795 |
rs758954614 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941312 | CACTTTGGAAAACAG[G/T]CTGGCAGTTCCTCAA | 388795 |
rs758972722 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897907 | CGCCTTTTCCATTCT[C/T]GTCACAGAGAGGAAA | 388795 |
rs759024537 | snp | A/C | 0.000101631 | 0.00712778 | missense | EFCAB8 | GRCh38.p7 | 20:32906880 | CATCCGCCTGTGGAA[A/C]CCCTTTGTCTCAAAG | 388795 |
rs759045005 | snp | C/G | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860809 | AGTGTTGTGATTACA[C/G]TTCACTACGGCCTCA | 388795 |
rs759069104 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888043 | GCTCTTCCATGGCTA[C/T]CCTCTCTACATATCC | 388795 |
rs759096351 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871390 | GCAATCCTCCTGACT[C/G]AGCCTCCAGAGTAGC | 388795 |
rs759098282 | snp | C/T | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860173 | GTTAGCTGGGCATGG[C/T]GGCGTGCACCTATAA | 388795 |
rs759112384 | snp | C/T | 0.000645548 | 0.0179543 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906547 | CCTGCAGCCCTCACT[C/T]CTTTGATATTGTAGG | 388795 |
rs759119691 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934754 | GCTCATGCTCTCTTG[A/C]CTGCTCCCATGTAAG | 388795 |
rs759131139 | snp | C/G | 0.000121264 | 0.0077857 | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859056 | AAAGATTGGATACCT[C/G]TGCTGAAGACCTCTG | 388795 |
rs759159258 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944038 | TTGCAAATCATATAT[C/G]TGATAAAGCATATTC | 388795 |
rs759182585 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937117 | TGTAATAAAATTAAG[A/C]ATTTTATTTTATTTT | 388795 |
rs759210331 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951275 | GCCTCAAACTAGAAA[C/T]GATTCAAATGTCCAT | 388795 |
rs759220767 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921512 | TGAACCATTATACCC[A/G]GCCTCTTCCTTCTCT | 388795 |
rs759251811 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942716 | CTGTTTATCACTTTC[A/T]TAGAGAAAAGATAAA | 388795 |
rs759264347 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955456 | GAGGCAGGAGGATCG[C/G]TAGAGCCCAGGTGTT | 388795 |
rs759285266 | in-del | -/CCCTC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929460 | TCTTTTTTCTCCCTT[-/CCCTC]CCCTCCCCTCCCCTC | 388795 |
rs759296335 | snp | G/T | 9.22807e-05 | 0.00679204 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906663 | ACCCAGAAGCTGCTG[G/T]GGGGAGGGCTGCTGG | 388795 |
rs759308287 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917965 | CAGGGGTTTTCCAAA[G/T]GTACTGGAGAGAGAT | 388795 |
rs759319766 | snp | A/C | 0.000295406 | 0.0121497 | missense | EFCAB8 | GRCh38.p7 | 20:32930419 | TTCCTGCAGACCAGG[A/C]CTCGCCTGCCGCACA | 388795 |
rs759338846 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953815 | TTGTGGTTTTTGTTT[G/T]TTTGTTTGTTTTGAA | 388795 |
rs759344564 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958557 | GAGCTGCAGTGAGTG[-/A]AGCACAGCCTGCTTG | 388795 |
rs759366946 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910892 | ACAGGCATGCACCAC[C/T]ACCCCCAGCTAATTT | 388795 |
rs759386450 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905196 | TCCTGACCCCTGTGC[A/G]GGAGGAGTAATATTT | 388795 |
rs759424788 | snp | A/G | 8.66063e-05 | 0.00657994 | missense | EFCAB8 | GRCh38.p7 | 20:32930569 | GCCATGGCCACTGAT[A/G]AAAATGACTGGATCC | 388795 |
rs759436682 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865455 | TGAATGCTACACTCC[G/T]GAGTTGGGGTGAAGA | 388795 |
rs759452771 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917192 | CCGACACCTGAGAGT[A/G]TCCTCCTCTGAGTCG | 388795 |
rs759492111 | snp | C/T | | | downstream-variant-500B | EFCAB8 | GRCh38.p7 | 20:32962293 | CCTCTGGACATATCA[C/T]CTGCAGCCTGAAGGG | 388795 |
rs759515679 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889414 | AAAGATAGGTGAGTC[A/C]CTGGGGGCTTCCCAG | 388795 |
rs759520438 | snp | A/G | 9.1638e-05 | 0.00676835 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889417 | GATAGGTGAGTCCCT[A/G]GGGGCTTCCCAGCTC | 388795 |
rs759539099 | in-del | -/AGCAT | 7.81586e-05 | 0.00625085 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912875 | TTCCTGTGAGTAGAA[-/AGCAT]GTATGGTGAGTAGGT | 388795 |
rs759545942 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875323 | GATGTGAGGAGGGGA[A/G]ACAGGGCCAAGAGGG | 388795 |
rs759564211 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901032 | AACCAAACAGTGCAC[-/T]GTGTACATTTCTAGA | 388795 |
rs759590456 | snp | A/G | 0.000181951 | 0.00953636 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893131 | CAGGTGTGAGCCACC[A/G]CGCCCAGCCCACACA | 388795 |
rs759593187 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890735 | AAAGGACCTGGGTTC[-/A]AGGGCCTGGTCCCAC | 388795 |
rs759655361 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931111 | GAATGGTCTGGGAGG[A/G]GCCCGCAGAGTGAGT | 388795 |
rs759656865 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902205 | ACTGGTGTGGTCTGG[C/T]TTATATGTTGCAGGT | 388795 |
rs759734397 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925759 | CATGAAGTTTAGCCC[G/T]TGAGTAGCTTGCCAT | 388795 |
rs759766322 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912558 | CTTGCCCATTTCCCA[A/G]CTATCCTCTCTGTAA | 388795 |
rs759769965 | in-del | -/TC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922815 | GAGAATGAGTACTTC[-/TC]TCTCTCTCTCTCTGT | 388795 |
rs759822436 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940339 | AAATAATATATTTTT[C/T]AAAACATGTCCTGCT | 388795 |
rs759829811 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861710 | GCAAAACCAGCCTGG[A/G]CAACATTGCAAGACC | 388795 |
rs759887879 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882941 | ACCTCATGATCTGCC[C/T]GCCTCGGCCTCCCAA | 388795 |
rs759905367 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887500 | AGAATCACTGGAACC[C/T]GGAGGCAGAGGTTCC | 388795 |
rs759978084 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947763 | GAAAAAAGTTCAAAT[C/T]TCCAGCCTCAACTTC | 388795 |
rs759984992 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863542 | GGCTTCTGCAGGACA[A/G]CTCCTCTCTATCAGG | 388795 |
rs760014516 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893159 | ACAACCTCTTCCGTC[G/T]CCATCTTTCTGCAGG | 388795 |
rs760033741 | snp | A/G | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859241 | CCCCTGTTCTGGATG[A/G]TACTCTCCCACCTGC | 388795 |
rs760036436 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933733 | CCTGTAATCCCAGTA[A/C]TTTGGGAGGCCGAGG | 388795 |
rs760108062 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870260 | GCCAGGAAGTGCCAC[A/C]ACTGTGTCTGGGAGG | 388795 |
rs760142313 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941080 | AGCATGGTGTAACCC[C/T]GTCTCTACTAAACAT | 388795 |
rs760167361 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895568 | TATCTTTTTTCTTTC[C/T]TTCTTTCTTTTTTTT | 388795 |
rs760182943 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920447 | TGATAAAGGCATATC[C/T]GAGACTGAGAAGAAA | 388795 |
rs760246398 | snp | A/G | 9.25198e-05 | 0.00680083 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906529 | GGGGCCACTGCTCCC[A/G]GCCCTGCAGCCCTCA | 388795 |
rs760248956 | snp | C/G | 0.000102833 | 0.00716979 | missense | EFCAB8 | GRCh38.p7 | 20:32959902 | CTGCAGAAGATGGCC[C/G]TGATGTCCCCGTGGG | 388795 |
rs760287916 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881663 | AGGGACATCGGGTTC[A/G]GCCACTGTGCCTATC | 388795 |
rs760338479 | in-del | -/TATT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929123 | AGTGTTCATAAGGGA[-/TATT]TATTTCTCTGTAGTC | 388795 |
rs760341919 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908230 | AGGAGCCGGCTACAT[C/T]CCCGAGACCCATGCT | 388795 |
rs760342983 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933445 | CAATTAACATATCTA[C/T]CACCTCACTTACAAT | 388795 |
rs760366369 | snp | A/G | 9.22977e-05 | 0.00679267 | missense | EFCAB8 | GRCh38.p7 | 20:32892237 | ATATTAGTGACCACA[A/G]ATGTGTCCGGGCCTT | 388795 |
rs760513442 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934290 | CAGGATTTTTTTTCT[A/C]TTTTAAGGCTGAATA | 388795 |
rs760613691 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887817 | CTGAGTGCTGGGCAC[C/T]ACCCTCAATGCTTCA | 388795 |
rs760614520 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885922 | GCTGTCCCTGCCCAC[C/G]AGGTTTCCTTCTCTT | 388795 |
rs760652929 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910310 | GGCATCTCTTTGCAG[A/G]GAAGCCATAACTTGG | 388795 |
rs760663072 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886942 | AAACTCCCTAGGGCT[C/T]TTGGTTTCTCTGAAT | 388795 |
rs760674897 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942259 | ATTTTAATTAAGATG[C/T]CTTTGTTTATTAGTG | 388795 |
rs760688832 | snp | A/G | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860008 | CTTTCTTTGGTTTAC[A/G]TGGCATTTTATTTTG | 388795 |
rs760711646 | snp | A/G | 0.000126976 | 0.00796693 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930363 | GTGACAGTGGCTCAC[A/G]GCCCTGCTGAGCCGG | 388795 |
rs760743699 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924736 | ATTTGTATCATGAAT[C/T]TTGATTGAATTTTTG | 388795 |
rs760805191 | snp | A/T | 9.21362e-05 | 0.00678672 | missense | EFCAB8 | GRCh38.p7 | 20:32885560 | CACCGGTTCAAGAAG[A/T]TCGGGTGTTTCCTGA | 388795 |
rs760808419 | in-del | -/TATGT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956256 | TATTTTATTTCTACA[-/TATGT]TATGTCTTCCTATAA | 388795 |
rs760817200 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903703 | GCTTTGATTTTTAGA[A/G]GAATCCTTGTGTCTC | 388795 |
rs760822052 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936312 | GTGCTGGGATTACAC[A/G]TGTGAGCCACCGCGC | 388795 |
rs760864092 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895447 | CTCCCACCTTAGCCT[C/T]CCAAGTAGCTGGGAC | 388795 |
rs760874117 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885094 | AGTTGCTAGAAAGTG[C/T]TGTTTCTCAGTTTTC | 388795 |
rs760887539 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924480 | AATGTATGTGAAAAG[A/G]ATGTTTAATACATCT | 388795 |
rs760932425 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882735 | GAGCCTTGCTCGGTC[A/G]CCCAGGCTGGAGTGC | 388795 |
rs760949396 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937254 | CAAAGTGCTGGTATT[A/T]GAAGCATGAGCCACT | 388795 |
rs760963669 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952298 | TCAGAAGTTTTAAAT[G/T]TTGGCATTGTATGCA | 388795 |
rs760983195 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867869 | TTTTTGAGACAGGAT[A/G]TTGCTCTGTCACCCA | 388795 |
rs761048939 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892018 | ATTCCAGCTGCAGTT[A/G]GAAGCCTTTGGGGAT | 388795 |
rs761070500 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932439 | GTATATCATACATCA[A/G]TGAAAGTTTTAAAAA | 388795 |
rs761090156 | snp | C/T | 0.000180196 | 0.0094903 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32961112 | CTGGTGCCCCATTCC[C/T]GCTCCCCACTCTGTT | 388795 |
rs761120556 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874093 | GCCTGGCTAATTTTT[G/T]TATTTTCTGTGAAGA | 388795 |
rs761126747 | snp | A/G | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860227 | GCATGAGAATCATCA[A/G]AATCTGGGAGGTGGA | 388795 |
rs761183306 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945601 | CCTCAATTTCTTTAG[C/T]GGCAGTTTCTGGAGA | 388795 |
rs761189500 | in-del | -/CT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939207 | TTCTTTCTTTCCTCT[-/CT]CTCTCTCTCTCTCTC | 388795 |
rs761192360 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952871 | ACCATTTTTAAGTCT[A/G]CAGTTCAGTAGTGTT | 388795 |
rs761219391 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947087 | TATGAATGAAGCCGC[C/T]TTAAACATTGTTTTC | 388795 |
rs761223382 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867443 | AAAATGGTTAAGAAT[C/T]CTGTATTTCTGTCAG | 388795 |
rs761233019 | in-del | -/TCTG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944457 | GCAACAGAGTGAGAC[-/TCTG]TCTAAAAAAAAAATA | 388795 |
rs761266894 | in-del | -/GCAGAGTCTT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895593 | TTTTTTTTTTTTAAG[-/GCAGAGTCTT]GCTCTATTGCCCAGG | 388795 |
rs761283862 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885201 | CTGTCTCCTCTGTCC[C/T]ATCACGTCGCGAGGA | 388795 |
rs761292764 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861731 | TTGCAAGACCCCATC[G/T]CAAAAGATCGCCATG | 388795 |
rs761296895 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912161 | TGTACTTAGCTGGCC[A/G]GGCAGTGGCTCACGC | 388795 |
rs761302859 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932194 | GACCAGCCTGGCCAA[C/T]CTGGTGAAACCCTGT | 388795 |
rs761307916 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913986 | ACAGATTTGGGGAGC[C/G]TTGCCCCCATGGTGG | 388795 |
rs761324708 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881630 | ATTTATTTTTACCCA[A/T]ACTTTTCCTCCTTTG | 388795 |
rs761338974 | in-del | -/AAAC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950011 | TCTCAAAAACAAACA[-/AAAC]AACAAAACAACAACA | 388795 |
rs761372431 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908178 | TGGACGGACGATGTG[C/T]CCTGGCCTTGTTCGC | 388795 |
rs761392802 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946629 | ATCTTTTAGAAGCTT[A/G]TTTTAAAAATCAGAT | 388795 |
rs761427333 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883604 | ATCAGATAAAAGCAA[-/C]CCATTTGAACATGAA | 388795 |
rs761463299 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919474 | GAAATGGGTGCATAG[A/G]TATATTTGCCCCTCT | 388795 |
rs761486890 | snp | C/T | | | missense | EFCAB8 | GRCh38.p7 | 20:32918528 | CGGCTCCCCCAGTGA[C/T]GCGGTGCCCGAGAGA | 388795 |
rs761536415 | in-del | -/T/TTTT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929502 | TTCTCTTCCCTTCTG[-/T/TTTT]TTTTTTTTTTTTTTT | 388795 |
rs761547652 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930700 | CATGGCCCTTGCCTA[A/G]TTCCTACTCTGTCTG | 388795 |
rs761569995 | in-del | -/GTGT | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860450 | GTATCGGATCAGGAG[-/GTGT]GTGATGGATGTCATT | 388795 |
rs761617712 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861519 | GTCTTGAACTCCTGA[C/T]ATCAGGTGATCCGTC | 388795 |
rs761627072 | in-del | -/CAGA | 9.7924e-05 | 0.0069966 | frameshift-variant | EFCAB8 | GRCh38.p7 | 20:32918552 | CGAGAGACAAGGAGC[-/CAGA]CAGGCCTGTGCCCCA | 388795 |
rs761641029 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925879 | GCTCACCTTCAGTCC[A/T]GCAGCTCTTTCCAAA | 388795 |
rs761737430 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886025 | TCCCCACGTCCTACC[A/G]ATTCAGGCCTTTTGC | 388795 |
rs761746933 | snp | A/T | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859129 | GCTGGCTTTCAATGC[A/T]TGTATCCTTAAGTCA | 388795 |
rs761749060 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937897 | GCTGGGATTACAGGC[A/G]TGAGCCACCACACCT | 388795 |
rs761761008 | snp | C/T | 8.94414e-05 | 0.00668676 | missense | EFCAB8 | GRCh38.p7 | 20:32896471 | CACTGGATCAAAGTT[C/T]CCTTGCAGAAACTCT | 388795 |
rs761825521 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954016 | TCATCACTTTGGCCA[C/G]GCTGGTCTCGAACTG | 388795 |
rs761865753 | snp | C/G | 0.000101994 | 0.00714049 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918585 | AGCAGGTGGGAGCGA[C/G]AGCCCAACCAGAAGG | 388795 |
rs761954215 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894324 | CCCCTGCTGGCAGAG[C/G]AGGGACAGATCCTGT | 388795 |
rs761968697 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890617 | GAGCAGACCTGTAAG[A/G]TGGTCAGGGAGAGGG | 388795 |
rs761999236 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866381 | CCACTCAGGTCATCT[A/G]ATTATCCACGTTAGA | 388795 |
rs762001225 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922020 | TTCTAGTAGAGTCGG[A/G]GTTTCACCATGTTGG | 388795 |
rs762120654 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934990 | TCACCAACACTTGTT[C/T]CTTGTCTTTTTGATA | 388795 |
rs762122875 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951241 | ACATAAATGTTCACA[G/T]CAGTATTTTTTTGTG | 388795 |
rs762129537 | snp | G/T | 9.23063e-05 | 0.00679298 | missense | EFCAB8 | GRCh38.p7 | 20:32885511 | CTCCCACAGGAACCA[G/T]GGCTGTGAGGTGGTG | 388795 |
rs762187257 | in-del | -/TT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895315 | TATTTTATTTAAGAT[-/TT]TTTTTTTTTTTTTTT | 388795 |
rs762228084 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899505 | AGAAGGTTGGAGTCC[C/T]GAGGGGCCCCCTCCT | 388795 |
rs762232581 | snp | A/G | 0.000204834 | 0.0101181 | missense | EFCAB8 | GRCh38.p7 | 20:32906902 | GTCTCAAAGAGGCCC[A/G]TGTGGCTGATGAAGG | 388795 |
rs762257026 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923430 | GGCGGAGGTTGCAGT[A/G]AGCTGAGATCGTGCC | 388795 |
rs762378302 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884891 | ACTTGGGTGCAGGGA[A/G]GCAACCCACAGAGGG | 388795 |
rs762378420 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872215 | GAGCCAGATTGCTAG[A/G]GTTAGTATCTGGTGC | 388795 |
rs762418800 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861540 | GTGATCCGTCTGCCT[C/T]GGCCTCCCAAAGTGC | 388795 |
rs762440969 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889568 | TAGGCAGGGGGTGGT[C/T]GGTGAATGCTCGAAT | 388795 |
rs762446961 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937222 | AGACCTCAGGTGATC[C/T]GACTGCCTCGGCCTC | 388795 |
rs762504707 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945398 | TTGAGCTCAAGTGAT[C/T]GCCCACCTAAGCTTC | 388795 |
rs762528188 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912430 | GAGTGAAACTCTGTC[-/A]AAAAAAAAAAAAAAA | 388795 |
rs762568612 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880017 | GCCCGGGTCACTGGA[C/T]CCCTTCCTGCAGTCC | 388795 |
rs762571097 | snp | A/G | 9.127e-05 | 0.00675475 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912756 | GAGCCATTTTCTCTG[A/G]TAAGTTTTCTAGTTC | 388795 |
rs762608395 | snp | G/T | 9.04282e-05 | 0.00672353 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896443 | TGGACCTTGGTTTTT[G/T]CCCCTATCAGATCAC | 388795 |
rs762609070 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941650 | ATTCTGCTTAAATGA[C/T]ATGTCCAGAATGTCC | 388795 |
rs762642109 | in-del | -/TTTG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942261 | TTTAATTAAGATGCC[-/TTTG]TTTATTAGTGATGTT | 388795 |
rs762692777 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929647 | ATGAGATTTTTGATA[A/G]TCGAGATTTTTGTTG | 388795 |
rs762700415 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937852 | TCGAACTCCCAACCT[C/T]GTGATCCGCCCACCA | 388795 |
rs762722489 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908007 | CCCAGCCAGTGAATT[A/C]AGCTGCTCCAACAGG | 388795 |
rs762742332 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895489 | CACCACCACTTCTGG[A/C]TAATTTTTTATTTTT | 388795 |
rs762880946 | snp | A/G | 6.99227e-05 | 0.0059124 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931158 | GGGTGTGAGGCCACT[A/G]ACCCACACTTTATGT | 388795 |
rs762978054 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918071 | GCTTTGGAGCTTCCA[C/T]TGAGATTAAAGGTAG | 388795 |
rs763080849 | snp | A/G | | | missense | EFCAB8 | GRCh38.p7 | 20:32893283 | CCCCGTATCCTCCCC[A/G]GGGCCTCCAAGTGGG | 388795 |
rs763197727 | snp | A/G | 0.000189072 | 0.00972112 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885474 | GAGCTGTTTTTGCTT[A/G]GGCTCTTCTCTCTTT | 388795 |
rs763222113 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922077 | CAGGTGATCCACTGG[C/T]CTCGGCTTCCCAAAG | 388795 |
rs763242119 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948141 | ACCAATATCAGGAAT[G/T]AGTGAGATGACATCA | 388795 |
rs763275158 | snp | A/T | 9.85367e-05 | 0.00701845 | missense | EFCAB8 | GRCh38.p7 | 20:32918557 | GACAAGGAGCCAGAC[A/T]GGCCTGTGCCCCAGC | 388795 |
rs763278943 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888549 | TTTGTAGAGATGGGG[G/T]CTCCCTATGTTGCCC | 388795 |
rs763287322 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870573 | GTGTGATCATAACTC[A/G]CTGCAGCCTTGAACT | 388795 |
rs763315864 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867283 | ACTGAACTGAGGTCC[C/G]TTATAAATGAACACC | 388795 |
rs763362690 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862884 | CAATCCTTCCGCCTT[-/G]GGCCTCCCAAAGTGC | 388795 |
rs763365246 | snp | A/G | | | missense | EFCAB8 | GRCh38.p7 | 20:32909846 | TAAAAGGGTACTTAG[A/G]GGCCCAGGGGCTTAT | 388795 |
rs763390432 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934884 | GTCTCGGATATGTCT[A/T]TATTAGCAGCATGAG | 388795 |
rs763433053 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923370 | ATACTCCTGTAGTCC[C/T]AGCTAGTCGGGAGGC | 388795 |
rs763512022 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878285 | GGAAAAAAAAAAGGC[C/T]GGGTGTGGTGGCTCA | 388795 |
rs763552703 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911271 | TTAACAGGTCTTCAC[C/T]AAACGTTCCAGTGCG | 388795 |
rs763586771 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951327 | ATGGTTTATGGAATA[C/T]CACTCAGCAATAAAA | 388795 |
rs763646138 | snp | G/T | 9.33576e-05 | 0.00683155 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863770 | TTAAGTTGACTATGA[G/T]TCCCTATTCTAGGTC | 388795 |
rs763648466 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918075 | TGGAGCTTCCATTGA[A/G]ATTAAAGGTAGCCTC | 388795 |
rs763686342 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878286 | GAAAAAAAAAAGGCC[A/G]GGTGTGGTGGCTCAT | 388795 |
rs763804243 | snp | A/G | | | missense | EFCAB8 | GRCh38.p7 | 20:32930548 | AATGGGGATGTTGTC[A/G]TGGGTGCCATGGCCA | 388795 |
rs763833300 | snp | A/C | 0.000158341 | 0.00889636 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931162 | GTGAGGCCACTAACC[A/C]ACACTTTATGTCTAG | 388795 |
rs763876538 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910301 | CTGTTCTTGGGCATC[-/T]CTTTGCAGGGAAGCC | 388795 |
rs763882609 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895512 | TTATTTTTTTGATTT[C/T]TTTTTGTAGAGATGG | 388795 |
rs763888130 | snp | A/G | 9.48272e-05 | 0.0068851 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32930436 | TCGCCTGCCGCACAC[A/G]GCTGCCCTGCTGAGC | 388795 |
rs763916910 | snp | C/G/T | 0.000179828 | 0.00948091 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896451 | GGTTTTTTCCCCTAT[C/G/T]AGATCACTGGATCAA | 388795 |
rs763940183 | snp | C/T | 0.000102433 | 0.00715583 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32906901 | TGTCTCAAAGAGGCC[C/T]GTGTGGCTGATGAAG | 388795 |
rs764004627 | snp | A/G | 9.06331e-05 | 0.00673115 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893142 | CACCGCGCCCAGCCC[A/G]CACAACCTCTTCCGT | 388795 |
rs764021677 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920942 | CCGAACACGAGTTGG[A/G]TATGGGTTCATCTTT | 388795 |
rs764029918 | in-del | -/CTC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862028 | TTGTAGCGTCCCATT[-/CTC]CTAGCTGTCTTGTGT | 388795 |
rs764031779 | snp | C/T | 9.25969e-05 | 0.00680367 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32918472 | CTCCAGTCTCAGCCC[C/T]GAGTCTGTGGCCAAT | 388795 |
rs764063253 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952707 | GTGAGTACTTTTATC[A/G]GTGTATCACTTGCCC | 388795 |
rs764073066 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936372 | CTTTTGGGGTCATAG[C/G]TAAATAACCATTGCT | 388795 |
rs764115184 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867987 | GACTACATGCACATA[C/T]CACCACTCCTGGCTA | 388795 |
rs764170164 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867134 | CATGTTGGTCAGGCT[A/G]GTCTCAAACTCCTGA | 388795 |
rs764173128 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934912 | GAGAACAGACCAATA[C/T]AGTGGTTGTACTGAT | 388795 |
rs764175235 | snp | C/G | 9.30882e-05 | 0.00682169 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875909 | AGGGGATGATGCTCT[C/G]TGTTCTCTCTTTGAA | 388795 |
rs764208452 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920292 | GGTCAGGATGGGGCT[C/T]GGGGGCCTGGGCTCG | 388795 |
rs764224462 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915489 | ACCAGAATGGTCTTT[A/T]ACATCCATATTTCTA | 388795 |
rs764263956 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895672 | GCCTTTCGGGTTCAA[-/G]GTGATTCTCCCGCCT | 388795 |
rs764296471 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863726 | CCTGGCTAAGTCAGC[C/T]TTCCACGTGGTCCTT | 388795 |
rs764303967 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886013 | ACTCCCACGCTGTCC[A/C]CACGTCCTACCGATT | 388795 |
rs764305253 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893368 | TGCTGAGGTCATCCT[C/G]GTCCCCGAGCCCCCC | 388795 |
rs764326042 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951449 | GTATGATTCTATTTA[-/T]TTTTTCCCAACCATT | 388795 |
rs764347876 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862756 | CCTCAGCCTCCCAAG[C/T]AGCTGGGATTACAGG | 388795 |
rs764356444 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892393 | GGCCCCCAGAAAGCC[G/T]CCTTGGAAAGATCTG | 388795 |
rs764392175 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957002 | TATTTTTTTGCTGAC[C/T]TGCCTTCCAGTTCAC | 388795 |
rs764424407 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875618 | CAAGGGATTCTCCTG[C/T]CTCAGCCTCCCAAGT | 388795 |
rs764456532 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948645 | TAAATACAAAATATC[G/T]TAACAAAATTTTGCA | 388795 |
rs764505663 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898711 | CTGACAGTGGCAGAT[A/G]GTGGTTGGTGTATGG | 388795 |
rs764538463 | in-del | -/TTT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870860 | TTCTACTTCTTCTTC[-/TTT]TTTTTTTTTTTCCTG | 388795 |
rs764546834 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943279 | GTCAGTGAGAATTAT[A/G]TACTTCTTATAAGGT | 388795 |
rs764552271 | snp | C/T | 9.21532e-05 | 0.00678735 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906557 | TCACTCCTTTGATAT[C/T]GTAGGTTGTCAGTGC | 388795 |
rs764626261 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883809 | GATTCTCCTGCCTCA[A/G]CCTCCTGAGTAGCTG | 388795 |
rs764629387 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933376 | TTGTAGACATTTCTG[A/T]GGCACAGTGTGCTGT | 388795 |
rs764659380 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870596 | CTTGAACTCCTGGGC[G/T]CAAGTGATCCTCCTG | 388795 |
rs764699091 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955645 | TATTCTTGAAGAAAC[C/T]CCAAGAAGGGCTTGA | 388795 |
rs764711449 | snp | G/T | 9.51158e-05 | 0.00689557 | missense | EFCAB8 | GRCh38.p7 | 20:32960119 | CTTGCAGAATACCAG[G/T]TTCCTGTCCACCAGG | 388795 |
rs764733404 | snp | C/T | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860820 | TACAGTTCACTACGG[C/T]CTCAAACTTCTGGAT | 388795 |
rs764749746 | snp | A/C | 0.000102349 | 0.0071529 | missense | EFCAB8 | GRCh38.p7 | 20:32906899 | TTTGTCTCAAAGAGG[A/C]CCGTGTGGCTGATGA | 388795 |
rs764809734 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936509 | GTGTGAGATAAGGAT[-/C]CAATTTTATTCTTCT | 388795 |
rs764835810 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888174 | GGTCAAGGGATCTTT[C/T]CACCTCAGCCTCCCA | 388795 |
rs764873712 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944124 | CAAACCAGAAGGGTT[C/T]AGCTTGGTGAATTTT | 388795 |
rs764886807 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897965 | GTCCAGGTCACAGAG[G/T]TGGCGCCGGAGAATT | 388795 |
rs764972476 | snp | C/T | 9.21107e-05 | 0.00678578 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920062 | TGGTGACTTGGGTGC[C/T]CATCTTTCTTTCCAG | 388795 |
rs764978155 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906692 | GGGGATGGGGGGACC[A/G]CCAGAGCTCAGGAGA | 388795 |
rs765034791 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942829 | GATAAAAGATAACAA[C/T]GTAGGTTTCTCTTAT | 388795 |
rs765075908 | snp | A/G | 8.69527e-05 | 0.00659309 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32930592 | CTGGATCCTCATCAC[A/G]GGGGATTGTAAAGGA | 388795 |
rs765085237 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865470 | GGAGTTGGGGTGAAG[A/T]GTGTCAGAAGCAGGG | 388795 |
rs765101820 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951299 | TGTCCATCAATAGTT[G/T]AGTTGATAAACTATG | 388795 |
rs765126134 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950152 | TTGCATGCAACACCG[A/G]TAGAGCATGATTCAT | 388795 |
rs765141348 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866660 | CATCTGACCGAGATG[A/G]GACATCTGGGCTGGT | 388795 |
rs765179267 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906399 | GGGTGAACCCTGGGT[A/G]GTCTCTGGGGCTACT | 388795 |
rs765237961 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932575 | TTCCTCTGGTGTTTA[C/T]TTATGCAAACACGAT | 388795 |
rs765248424 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862691 | AGAGTACAATGGCTC[A/G]ATCTCGGCTCATGGC | 388795 |
rs765269997 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868456 | ATTTGGGATCTAGAA[A/G]ATTTTTAAAAATACC | 388795 |
rs765270028 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893033 | TTTAGTAGAGATGAG[C/G]TTTCACCACGTTGGC | 388795 |
rs765272895 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931137 | TGAGTTGGGGTCTGG[A/G]TCAAGGGGTGTGAGG | 388795 |
rs765317176 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876680 | CTATTACTTACCTCT[A/G]TTTCGGCCGGGCACA | 388795 |
rs765415047 | snp | C/G | | | missense | EFCAB8 | GRCh38.p7 | 20:32961285 | CCTGGTGCCCAGCAG[C/G]GAGCAGGCTGTGCTG | 388795 |
rs765440854 | in-del | -/ATGT | 0.000178079 | 0.00943438 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912878 | CTGTGAGTAGAAAGC[-/ATGT]ATGGTGAGTAGGTTC | 388795 |
rs765442052 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874315 | TCAGCCTCTGCCTCC[C/T]GGGTTCAAGCCATCC | 388795 |
rs765445756 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908525 | CTCCTGGGACTGCTG[-/A]AGCGGCTAGACTCTG | 388795 |
rs765457580 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948567 | AAAGAAAGAAAGAAA[-/A]GAAAGAAAGAAAGAA | 388795 |
rs765470389 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908874 | CCTGTGGGAAACTGA[A/G]TCACAGATAGGAAGG | 388795 |
rs765495913 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886016 | CCCACGCTGTCCCCA[C/T]GTCCTACCGATTCAG | 388795 |
rs765496100 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873024 | CTTGAACCCAGGATG[C/T]GGAGGTTGCAGTGAG | 388795 |
rs765543773 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882946 | ATGATCTGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 388795 |
rs765704315 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920788 | AGGTGGAGTTGGGGT[A/G]CCTAGGGAAGTGAGC | 388795 |
rs765708969 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954231 | TGAAGCTTTTCCTCC[A/G]TATTTTTTCTAGGAG | 388795 |
rs765740625 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942367 | TATTGTGGTAACTAT[C/G]TTTTATAAATGTTGT | 388795 |
rs765743670 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917849 | CTACTACACATTACC[A/G]CTGTGGGCTCCCCAG | 388795 |
rs765774363 | snp | C/T | | | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32893222 | AGACGCCAAAGGCAA[C/T]GTCATTGTCTTCACC | 388795 |
rs765821613 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912642 | AATAGGATGTGAGAA[C/G]ATGATGACAAATACA | 388795 |
rs765831948 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912448 | AAAAAAAAAAAAGAA[-/G]GAAGAAGAAAGAAAG | 388795 |
rs765834027 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933749 | TTTGGGAGGCCGAGG[C/T]GGGCAGATCACCTGA | 388795 |
rs765854599 | snp | G/T | 9.23574e-05 | 0.00679486 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906538 | GCTCCCGGCCCTGCA[G/T]CCCTCACTCCTTTGA | 388795 |
rs765854772 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926136 | CCTACCTGCTCTCAC[C/T]GTCCCAGGGCTGGCA | 388795 |
rs765855434 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872577 | GAGGTGGGTGGATCA[A/G]GAGGTCAAGGGTTCG | 388795 |
rs765873704 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895575 | TTTCTTTCTTTCTTT[-/C]TTTTTTTTTTTTTTA | 388795 |
rs765880933 | snp | A/G | 9.42551e-05 | 0.00686431 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32960086 | AGTCTTGGGAGCGGC[A/G]TATAAGCCCAAGGAA | 388795 |
rs765904763 | snp | G/T | | | missense | EFCAB8 | GRCh38.p7 | 20:32892248 | CACAAATGTGTCCGG[G/T]CCTTCACCTTTGTTG | 388795 |
rs765922700 | snp | A/G | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859287 | TTCCGTCAGCTCCGG[A/G]CAGGTCAACTTTAGG | 388795 |
rs766009247 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869560 | AATCTTATATAACAA[A/G]TCATGTAATCATGTG | 388795 |
rs766033634 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908830 | GGGAAACAGGGGCCA[C/T]GTCCGAGCAGCATCT | 388795 |
rs766064734 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868807 | CTGGCCAACATGGTG[A/G]AACCCCGTCTCTACT | 388795 |
rs766077486 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896682 | CAGCTGTTGGATCCC[A/G]TCAGCTCTATCTGCA | 388795 |
rs766117682 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903780 | GCTGGGAGGCTGATA[C/T]GGCAAAGTCAGGGGC | 388795 |
rs766131759 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949989 | TGGGCAACAGAGCAA[G/T]ACTCTGTCTCAAAAA | 388795 |
rs766173907 | in-del | -/GCTC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935231 | TTGAGATGGCGTTTT[-/GCTC]TTGTTGCCCGGGCTG | 388795 |
rs766184555 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954134 | TGATACACAGAGGTT[C/T]TCAAGTTTAATGTCT | 388795 |
rs766215889 | snp | A/C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876578 | TAGCAAAGATGACAA[A/C/T]GATAACTAGCATTTA | 388795 |
rs766269545 | snp | C/T | 9.21617e-05 | 0.00678766 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32885562 | CCGGTTCAAGAAGAT[C/T]GGGTGTTTCCTGACT | 388795 |
rs766280351 | snp | A/G | 9.21871e-05 | 0.0067886 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920038 | CTATGGGGAAGGGAA[A/G]CACCCTCATGGTGAC | 388795 |
rs766297312 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948957 | AAGACATGTCACTTC[A/G]ATTCAAAATTATACT | 388795 |
rs766323249 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899820 | CTCAGGTTATCAGCC[C/T]GCCTCGGCCTCCCAA | 388795 |
rs766350324 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887857 | ATTCCATTCATTCCT[C/T]GCAACTTTGCAGAAC | 388795 |
rs766402541 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928539 | CGCACCCAGCCAATG[C/T]GACTGATTTTTATGT | 388795 |
rs766402695 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901572 | CTGCCTTCCTGACCT[C/T]ATTGCCTCCACCTGC | 388795 |
rs766437091 | in-del | -/AACCTCCAT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890493 | CCTCCTCCAGACTGG[-/AACCTCCAT]AAGGTCAGGGACTGC | 388795 |
rs766446033 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885116 | TCAGTTTTCAGCCTC[A/G]GGCTCCACTCTGCTC | 388795 |
rs766471011 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904605 | CACCTGAATGGAGCT[-/T]TTTTTTTTTTTTTTT | 388795 |
rs766475593 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32961131 | CCCCACTCTGTTCCC[A/T]GCAGATCTCGCCTCA | 388795 |
rs766490835 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925200 | CAGCTGTGTCCCTGA[C/G]AGTCTTTATTTTTAA | 388795 |
rs766597815 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919715 | TGTTGGCCAGGCTGG[C/T]CTCAGACTCCTGGCC | 388795 |
rs766646023 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895476 | ACCACAGGCACGCCA[C/T]CACCACTTCTGGCTA | 388795 |
rs766684942 | in-del | -/GAAG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912446 | AAAAAAAAAAAAAAA[-/GAAG]AAGAAGAAAGAAAGT | 388795 |
rs766685427 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892053 | AGTGGGGTTCCCGGT[A/G]GGTGGGTTTACTCTG | 388795 |
rs766702580 | snp | A/C | 9.41309e-05 | 0.00685978 | missense | EFCAB8 | GRCh38.p7 | 20:32863826 | GCAGAGATCCCTCAA[A/C]TCCAAAAGGTAAGAA | 388795 |
rs766738519 | snp | C/T | | | missense | EFCAB8 | GRCh38.p7 | 20:32875992 | TGTCGGACGAGATGC[C/T]AAAGGAGCTGTTTTT | 388795 |
rs766741428 | snp | C/T | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860434 | GCATTGTGCCCTGCA[C/T]GTATCGGATCAGGAG | 388795 |
rs766780400 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945145 | CAGCTCTAGAATTTC[A/T]GTTATTTTTATTATT | 388795 |
rs766804986 | snp | A/G | 9.01023e-05 | 0.00671141 | missense | EFCAB8 | GRCh38.p7 | 20:32917399 | GGAACCAGTTCCTTG[A/G]GACCTCCTCCTACAG | 388795 |
rs766859387 | snp | A/G | 8.87508e-05 | 0.0066609 | missense | EFCAB8 | GRCh38.p7 | 20:32912828 | TGAACAAAGTGTTCT[A/G]TGTGACAGGATGGAG | 388795 |
rs766904412 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942822 | GGTGTAAGATAAAAG[A/G]TAACAACGTAGGTTT | 388795 |
rs766982021 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862510 | CTTCCAAATCTCCTT[C/T]CCTTAGGCTGTCCTC | 388795 |
rs767027151 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895722 | GATTACAGGCACACA[C/T]CACCATGCCCGGCTA | 388795 |
rs767037028 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861744 | TCTCAAAAGATCGCC[A/G]TGAACCCTTTTTTAA | 388795 |
rs767085817 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880035 | CTTCCTGCAGTCCAC[C/T]CTGGAGCACTGCTGC | 388795 |
rs767092233 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908192 | GCCCTGGCCTTGTTC[A/G]CCGGAGGCACCCCCG | 388795 |
rs767212373 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878683 | AATACCCTGCCTCCC[C/T]TGTGCTTTCTTTCGA | 388795 |
rs767249460 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957670 | TGTGCATTCAGGCGA[C/G]ACTTAATTAATCATG | 388795 |
rs767290927 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914465 | GGCTATGTCTTTAAT[G/T]ATTGTATTAGTTTGT | 388795 |
rs767293758 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886121 | AGTCCTAACTGTACC[A/G]CCTGCAAGCTCTGTG | 388795 |
rs767329050 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874394 | CACCTGGCTAATTTA[A/C]AAAATTTTTTTTGTA | 388795 |
rs767410819 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925914 | GCAGGGCAATGTATT[A/G]GATGGGGCTGGATGC | 388795 |
rs767416379 | snp | A/G | | | splice-donor-variant | EFCAB8 | GRCh38.p7 | 20:32896528 | AGCTACCGGCTGAAG[A/G]TGAGTTTTTTCTTTC | 388795 |
rs767435429 | snp | A/G | 9.33489e-05 | 0.00683123 | missense | EFCAB8 | GRCh38.p7 | 20:32918498 | CCAATACCAACCTGA[A/G]GCGGAGCCTGGTGTC | 388795 |
rs767444699 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910117 | TACAGATGGGCTGGC[A/G]TGGGATCAGCTCAGA | 388795 |
rs767463891 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955016 | TGGACATCTATCCTC[-/C]CCATGAGTAGAGTGG | 388795 |
rs767468587 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929895 | GTAAGGGAAAAGTGA[G/T]CAGAGTGAGGAATTA | 388795 |
rs767470564 | in-del | -/C | 9.83816e-05 | 0.00701293 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960020 | GGAGGAGTGCAGGGA[-/C]CCCCCAACTCGCAGC | 388795 |
rs767471541 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867853 | AAGCATTTTTTTTTT[A/G]TTTTTGAGACAGGAT | 388795 |
rs767496546 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925085 | TGGGGGTCTTACCTG[C/T]TGGGTCTTCCTTCCC | 388795 |
rs767498774 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940821 | ATATTAAATGATGGT[G/T]AACATCATTAGCTAT | 388795 |
rs767539067 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952596 | CTCTTTGAGTATTTT[-/G]TTGTTTTTAAGAAAT | 388795 |
rs767582470 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957440 | GAGCATCTCCATCCA[C/G]TTGGGGATTGAACTG | 388795 |
rs767594616 | snp | A/T | 0.000102854 | 0.00717053 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918592 | GGGAGCGAGAGCCCA[A/T]CCAGAAGGCTACCCT | 388795 |
rs767647323 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898804 | TTTATCTCCCAATCT[A/G]TATGCAAAACTCAGC | 388795 |
rs767661034 | snp | A/C | 8.90908e-05 | 0.00667364 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32878755 | GGAAAAGAGGACATG[A/C]GAAAGAGCCAGTACC | 388795 |
rs767716425 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873086 | AATAAGAGCAAAACT[-/C]CCATCTCAAAGAGCA | 388795 |
rs767718266 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883075 | ATCTCAGGTGATCCA[C/T]CTGCCTTGGCCTCCC | 388795 |
rs767727419 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957690 | AATTAATCATGCCAG[A/C]CACAGTGGATGTCAG | 388795 |
rs767733774 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905096 | GCCCTCTGAGCCTCA[C/G]CCGGCCCTAATGAGC | 388795 |
rs767738123 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936232 | AGAGACAGGATTTCA[A/C]CATGTTGGCCAGGCT | 388795 |
rs767802610 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945556 | TTTTTATTACGGTTA[C/T]TTAGAATTCTTTGTC | 388795 |
rs767843379 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893433 | CGTCTGCTTCCAAGC[A/G]CAGGGTGCATGCCGC | 388795 |
rs767876925 | snp | G/T | 9.04609e-05 | 0.00672475 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912775 | GTTTTCTAGTTCTGT[G/T]TTCTTTCATCTTCAA | 388795 |
rs768054491 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862283 | GTATAGGCATGTGCC[A/G]CCACACCTGGCTAAT | 388795 |
rs768063296 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959420 | GGCATACATCTTGAC[A/G]GTACAGTGGAGGGAC | 388795 |
rs768132979 | snp | A/C | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860900 | AGTGTCACCATACCC[A/C]GATAATTTTTTGTAT | 388795 |
rs768160636 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946571 | TTTTTTTGTATCTTT[C/T]AAAGACGTCTTTGAC | 388795 |
rs768176723 | snp | C/T | 9.43352e-05 | 0.00686722 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32867731 | AATGTTTGAGGAGGA[C/T]ATCAACTCGACTGGA | 388795 |
rs768186482 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872239 | CTGGTGCTACCACTT[A/G]CCAGCTGTGTGACCT | 388795 |
rs768199984 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901629 | TCAGGCGTGCTCCTG[C/T]GCCAGGGCCTTTGCA | 388795 |
rs768210031 | snp | A/G | 8.75618e-05 | 0.00661614 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32876020 | TTTGAAGGTGGACTC[A/G]GACTGTGAAGGCTTT | 388795 |
rs768231373 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932046 | GCTCTGCTTCATTAA[C/T]GGGCCTGATCATGCA | 388795 |
rs768266732 | snp | C/T | 9.1916e-05 | 0.00677861 | missense | EFCAB8 | GRCh38.p7 | 20:32917354 | GGCAGACCTACCACA[C/T]GGAGGACATCCTGAG | 388795 |
rs768285706 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919967 | CAGGCCAGTGTACCT[A/G]CTGCGGGGGCTTGGG | 388795 |
rs768287833 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913438 | ACCTCCAAATTTCCT[C/T]GCCTTAGGGATTACG | 388795 |
rs768290862 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861424 | CTCCTGAGTAGCTGG[A/G]ATTACAGGCATCCAC | 388795 |
rs768292907 | in-del | -/T | 9.21022e-05 | 0.00678547 | frameshift-variant | EFCAB8 | GRCh38.p7 | 20:32867684 | CCTGGGTCCCAGCTG[-/T]TTACTGAGATACACC | 388795 |
rs768308473 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911816 | TCTGAAAGGGTGTTC[A/C]TCATAGTCAGGTGGC | 388795 |
rs768346341 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937171 | TTTTAGTAGAGACAG[G/T]GTTTCTCCATGTTGG | 388795 |
rs768346637 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882413 | CACCTCACACAGTTC[A/C]GGAATCAGTCCTGGG | 388795 |
rs768373447 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908487 | ATCCCATGGGACACC[C/T]AAGGGGTGGCCACGT | 388795 |
rs768377959 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940423 | CTCATAACACATACA[A/G]AAATTAACTCCAAAT | 388795 |
rs768385971 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954748 | TAAAAAAAATCATAA[A/G]TAGGTGTTGAATTCT | 388795 |
rs768409785 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945409 | TGATCGCCCACCTAA[A/G]CTTCCCAAAGTGTTG | 388795 |
rs768424440 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874027 | TCAGGCTCAAGCAAT[C/T]CTCCCAGCTCAACCT | 388795 |
rs768454719 | snp | C/G | 9.56343e-05 | 0.00691433 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960046 | GCAGCCTTCATTCTT[C/G]GGCGTGGCTCCTGCA | 388795 |
rs768460160 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885692 | GATTGGAGAGCCTCT[A/G]CCTTAGCACCCCCAT | 388795 |
rs768478228 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946767 | AGACATTACCCCAAA[A/C]AGTGACCTCATGTCT | 388795 |
rs768501765 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908210 | GGAGGCACCCCCGAG[G/T]CTTCAGGAGCCGGCT | 388795 |
rs768506402 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916688 | ACATAAATTTTTGGA[A/G]AATATGAATATTCAG | 388795 |
rs768508619 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896188 | ACCTAGGAAGCGTGA[A/G]GTGCCCTGAAATCTG | 388795 |
rs768584335 | snp | G/T | 0.000277585 | 0.0117778 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32959835 | AGAGCAGGCGGCGCT[G/T]ATGGCTCTCCTGCAT | 388795 |
rs768587148 | in-del | -/TTTTTTTTTTTTTT | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860496 | CTGATGGTGGTAACT[-/TTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 388795 |
rs768632278 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881494 | GAGCCACCGCATCCA[C/G]CCAGTCATCTCTTGC | 388795 |
rs768685204 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917709 | ATGGAGGCACACGGA[C/G]ATGAAGCACCTTGCC | 388795 |
rs768704897 | snp | C/T | 9.28203e-05 | 0.00681187 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898641 | AAGAAGTGCTTCTCT[C/T]CTGGCTAAGGCGGTG | 388795 |
rs768715146 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919296 | GAGAAACACCACCGT[C/T]CCCAAACACACAATA | 388795 |
rs768745045 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904887 | CCGCCTTGGTCTCCC[A/G]AAGTGCTGGGATTAC | 388795 |
rs768755694 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876459 | TTTTACAGCATCATA[A/G]TAATAATGCTTTCAT | 388795 |
rs768761441 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910146 | GAGCTCCATCCGTTA[G/T]CCATGGGATCGCCTA | 388795 |
rs768794030 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877623 | CCTAGCATTCTCAGG[A/G]CTTTACCCAGTGGTC | 388795 |
rs768800938 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951190 | GAATCAGCTGTTCCA[C/T]TTCTATGAAAGCATA | 388795 |
rs768809652 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867431 | TTCTTAGGTGTAAAA[A/G]TGGTTAAGAATTCTG | 388795 |
rs768833775 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925800 | AAGGGACCCACAGGG[-/A]AGGCCATTAACCCGC | 388795 |
rs768890091 | snp | A/G | 9.85756e-05 | 0.00701983 | missense | EFCAB8 | GRCh38.p7 | 20:32918558 | ACAAGGAGCCAGACA[A/G]GCCTGTGCCCCAGCA | 388795 |
rs768900511 | in-del | -/CTT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869485 | AGGTGATCCGCCTGC[-/CTT]AGCCTCCCAAAGTGC | 388795 |
rs768916767 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889048 | GGCAAGACTTTGATA[A/G]AACTGTGAGACTGCT | 388795 |
rs768957602 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890448 | AGTGTCATCTCACAT[C/G]TATTAGTTTGCTTCT | 388795 |
rs768958022 | snp | A/T | 9.38659e-05 | 0.00685012 | missense | EFCAB8 | GRCh38.p7 | 20:32920198 | ATGTTGGTTCAATCC[A/T]GTGCCTCGGTGGAGA | 388795 |
rs769021240 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923411 | GAATTGATTGAACCC[A/G]GGAGGCGGAGGTTGC | 388795 |
rs769023000 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924120 | GTGCAGTGGCACAAT[C/T]ACAGCTCATTGTAGC | 388795 |
rs769060405 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905991 | TTGGGGAAGCTCCTT[A/G]ACTTTTCCTTTTGGT | 388795 |
rs769126688 | snp | C/T | 9.36549e-05 | 0.00684242 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867574 | GGTTCTTGTTATATT[C/T]GTTCCAGCTGTCCAT | 388795 |
rs769215443 | snp | C/T | | | stop-gained | EFCAB8 | GRCh38.p7 | 20:32958453 | GTGTGGAAAAGACTA[C/T]AGGATGCCTGTGATG | 388795 |
rs769223074 | snp | A/C | 0.000184502 | 0.00960296 | missense | EFCAB8 | GRCh38.p7 | 20:32892234 | TTGATATTAGTGACC[A/C]CAAATGTGTCCGGGC | 388795 |
rs769253273 | snp | G/T | 0.000182532 | 0.00955157 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912752 | CCCAGAGCCATTTTC[G/T]CTGATAAGTTTTCTA | 388795 |
rs769333093 | snp | C/G | 9.25369e-05 | 0.00680146 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911754 | CGGCCTCTTGGGAAG[C/G]AAAGCACAGCTCCTT | 388795 |
rs769360605 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879924 | CCAGGGGTTGATCTG[C/T]CTCGCTGTGTGTTCC | 388795 |
rs769406321 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927748 | CACATTTTGTACAGT[A/G]AGCACTTGCATAAAG | 388795 |
rs769422930 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911125 | ATTCTCAACAGTTCC[C/T]TACTTAGGGGGCAGT | 388795 |
rs769431876 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881882 | AGGGAATTCTGACAA[C/T]GTTTTAAAACATGGT | 388795 |
rs769437356 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923331 | TCTCTACTAAAATAC[A/C]AAAAATTAGCCAGGG | 388795 |
rs769439319 | in-del | -/AA | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890002 | AGAGACTCAGTCTTA[-/AA]AAAAAAAAAAAAAAA | 388795 |
rs769474664 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871723 | TATGAGTGCGGGCTC[C/T]ATACCGTGTCTTAGG | 388795 |
rs769494173 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923861 | GCCGCTGGGTTTTGC[C/T]TCTATAGAAAGCATT | 388795 |
rs769529805 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883588 | TTCATTCCCATGATA[C/G]AATCAGATAAAAGCA | 388795 |
rs769550855 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949034 | TGGAAAGGAAGAAAT[-/A]AAAACTGTTTTTATT | 388795 |
rs769614861 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894914 | CAGCCCCACTCTGGC[A/G]GTCTTGGGCAACTTT | 388795 |
rs769618315 | snp | G/T | 0.000276281 | 0.0117501 | missense | EFCAB8 | GRCh38.p7 | 20:32867668 | GGTGCCTGACCTCCA[G/T]CCTGGGTCCCAGCTG | 388795 |
rs769695978 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862102 | AGTTTCAGTCCCCAG[A/G]TTTCCAGATACTTGT | 388795 |
rs769751311 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918031 | GGGTTTCCCCCAGAA[C/T]AGCTCAGCTTTTTAT | 388795 |
rs769790507 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900422 | CTGGAGTGCAGTGGC[A/G]CAATCTCGGCTCACT | 388795 |
rs769813529 | snp | A/G | 9.16464e-05 | 0.00676866 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896407 | CTTTGCTTGCCAAGC[A/G]AAGGGGGAAAGCTGC | 388795 |
rs769822614 | snp | A/G | 0.000147417 | 0.00858409 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32959829 | GCGGCGAGAGCAGGC[A/G]GCGCTGATGGCTCTC | 388795 |
rs769837963 | in-del | -/TTATTT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919493 | TTTGCCCCTCTATCC[-/TTATTT]TTATTTTTATTTTTA | 388795 |
rs769869865 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933208 | CCTAAGTCTGTCTGA[C/T]TCCAGAATCTGTGTT | 388795 |
rs769876418 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915368 | TACCTGTCTCAAAAC[A/G]CTAGAACACAAATAT | 388795 |
rs769898459 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909576 | TGAAAGGGACCTTGG[-/A]CTTGGAATTTGGGGT | 388795 |
rs770031486 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927875 | ATTTACCATTGAAAC[C/T]ATTTTTAAGTGTATG | 388795 |
rs770054283 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897760 | TGGTTTTCCCTCCAG[A/G]TCTCACTCAGTGTCT | 388795 |
rs770056631 | snp | A/G | 0.000100286 | 0.00708046 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959996 | AGGTGAGGCTGGGAG[A/G]GGAGCACAGGGAGGA | 388795 |
rs770065522 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941920 | CAAATATTCTTTTTC[A/T]CAAATGTTTTTTGTT | 388795 |
rs770092117 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921660 | CCATCCCACTCTCAA[C/T]AGCAGCATTCGCTGC | 388795 |
rs770117799 | snp | A/G | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859749 | CTTTTACCCCTAAAT[A/G]CTTTTCAGTGTACAT | 388795 |
rs770165995 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934723 | ATATGATGGCTTTAT[A/G]AAGGGCAGTTCCCCT | 388795 |
rs770187936 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936196 | TGCCACCATGCCTAG[C/G]TAATTTTTGTATTTT | 388795 |
rs770199169 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866009 | GGGACGGTAGAATGC[A/G]TAGGAAGAAGAGGGA | 388795 |
rs770204286 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887501 | GAATCACTGGAACCC[A/G]GAGGCAGAGGTTCCA | 388795 |
rs770307453 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951033 | ATACTAATTAAAACC[G/T]CTGTAAGATACCATT | 388795 |
rs770308990 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909625 | TGGAAGGCTCAGTCT[C/T]GGGGAGCGGGGGCCA | 388795 |
rs770310497 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867232 | GCCCCCTGGGGTTCT[C/G]AATTCTGACCACTGA | 388795 |
rs770323048 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876195 | GGGACTTGCCTGGTG[C/G]AGACGTCCCTCCTAA | 388795 |
rs770361014 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956729 | AGTTTGACTATGATG[-/T]GCGTAAGTGTGGTTT | 388795 |
rs770416471 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904865 | CTCCTGACCTCAGGT[A/G]ATCCGGCCGCCTTGG | 388795 |
rs770435001 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903065 | CATTTCCTGACCCAC[A/G]GCCATCAACAAATCT | 388795 |
rs770438273 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923120 | GTCTGGGAGGTCAAG[A/G]ATGCAGTGAGCTGTG | 388795 |
rs770484610 | snp | A/G | 0.00020319 | 0.0100774 | missense | EFCAB8 | GRCh38.p7 | 20:32906870 | ACGATGCCTTCATCC[A/G]CCTGTGGAACCCCTT | 388795 |
rs770568177 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882806 | GTTCATGCCGTTCTC[C/T]TGCCTCAGCCTCCCG | 388795 |
rs770588193 | in-del | -/TACAG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869144 | TGGTGGGAGGCTACC[-/TACAG]TACAGTTCCTGGCCA | 388795 |
rs770694584 | in-del | -/AAC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957186 | TTTAACATTATTTGT[-/AAC]AACAGTTATTTAAAG | 388795 |
rs770770526 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877882 | GATGCCAGTTGTGGG[A/G]GTGATCTGAGGATGC | 388795 |
rs770780722 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861353 | GAGTGCAATGGCACA[A/G]TCTCGGCTCACCGCA | 388795 |
rs770787494 | snp | C/G | 9.21701e-05 | 0.00678797 | missense | EFCAB8 | GRCh38.p7 | 20:32867615 | TTCCAGAACAAGGAG[C/G]CTGCTAGCTCCCCAA | 388795 |
rs770799678 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939694 | TTCCTTCTCTCTCTC[-/T]CTTTTTTTTTTCTTC | 388795 |
rs770871404 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929040 | AAAAGTCACTTGGTC[A/T]TGGTATATAATCCTT | 388795 |
rs770927942 | snp | A/G | 9.37954e-05 | 0.00684755 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892332 | TCCTCACATGAACCA[A/G]GAGGCCCAGGCCTCC | 388795 |
rs770932547 | snp | A/G | 8.68772e-05 | 0.00659022 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32930538 | GGACCTAGACAATGG[A/G]GATGTTGTCGTGGGT | 388795 |
rs770969954 | in-del | -/TC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939202 | CTTTCTTTCTTTCTT[-/TC]CTCTCTCTCTCTCTC | 388795 |
rs770981143 | in-del | -/G | 0.000192864 | 0.00981809 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898670 | TGGGGCTGGAAGGGA[-/G]GGGGGTGGTGAGTGG | 388795 |
rs770986165 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878688 | CCTGCCTCCCTTGTG[C/T]TTTCTTTCGAGGCAG | 388795 |
rs770988571 | snp | C/T | | | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32898576 | AGCCATCGAGAAGTC[C/T]TCTCTGGTGCTGACA | 388795 |
rs771023727 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885939 | GGTTTCCTTCTCTTG[A/C]GTCCCCATCTCAGTG | 388795 |
rs771081840 | snp | A/G | | | downstream-variant-500B | EFCAB8 | GRCh38.p7 | 20:32962340 | TGCTACTGAGCAAGG[A/G]GGAGGTGGGCTATAG | 388795 |
rs771101077 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871648 | TTCACCTTTTGTTGA[G/T]GTAGGATAAAGGAAA | 388795 |
rs771128080 | snp | A/G | 9.16045e-05 | 0.00676711 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896404 | AGGCTTTGCTTGCCA[A/G]GCGAAGGGGGAAAGC | 388795 |
rs771178244 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908428 | GTGAGTGCTGTCCCA[A/G]GAGGGAGTGGGGTCA | 388795 |
rs771208220 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863401 | AGCCCTCATTTTTCT[A/G]ATCTGTTTATTGTAC | 388795 |
rs771224419 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949349 | AAATTATCTCCAAAT[A/T]GATTTATAGGTTAAC | 388795 |
rs771257109 | in-del | -/AGT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916786 | GTGCTGTGAAAAAAA[-/AGT]AGGAGTTTCTATGGG | 388795 |
rs771280345 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864853 | TCACTATGAGACAAG[A/G]AGTAATAACAAGAGC | 388795 |
rs771318276 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948147 | ATCAGGAATGAGTGA[A/G]ATGACATCATTTCTG | 388795 |
rs771330812 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902045 | AAATGTTTCAAACAC[A/T]CACAAAAATAGATAA | 388795 |
rs771348727 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905950 | CCTAAACCCCATAAC[C/T]CCCATTGTTTGCAAC | 388795 |
rs771349406 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927634 | AGAGGCGAGAGCCAC[C/T]ATGCCTGGCCAAAAT | 388795 |
rs771390090 | snp | A/G | | | downstream-variant-500B | EFCAB8 | GRCh38.p7 | 20:32962013 | GACCGGCAGCCATCT[A/G]GTGAGGGTCATGGCT | 388795 |
rs771441427 | snp | A/G | 7.27564e-05 | 0.00603099 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878810 | CGGTCGTCCCCCTGT[A/G]AGGAGCCTCTTCCTG | 388795 |
rs771464125 | in-del | -/TTTTTTTTTTTTTTT | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860494 | GCTGATGGTGGTAAC[-/TTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 388795 |
rs771550569 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915059 | CATGCCACCATGCCT[A/T]GCTAATTAAAAAAAA | 388795 |
rs771571300 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913551 | GCAAAATATATTCAT[C/T]TCATCCCAATAGCCC | 388795 |
rs771589351 | in-del | -/CC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955015 | CTGGACATCTATCCT[-/CC]CCATGAGTAGAGTGG | 388795 |
rs771590379 | snp | G/T | 9.42463e-05 | 0.00686398 | missense | EFCAB8 | GRCh38.p7 | 20:32960077 | GGTGAGCAAAGTCTT[G/T]GGAGCGGCGTATAAG | 388795 |
rs771592253 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881639 | TACCCAAACTTTTCC[G/T]CCTTTGCAAGGGACA | 388795 |
rs771594640 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933390 | GAGGCACAGTGTGCT[A/G]TTTTGATCTATGTAC | 388795 |
rs771621055 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902877 | GCAAATCTGACGGAG[C/T]GGGTGTGGTAGCAGG | 388795 |
rs771643161 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891953 | CTTGCCTTAGCCTCC[C/G]TAAGTGCTGGGATCA | 388795 |
rs771668681 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885042 | TTTGATTTCATCCTT[C/T]GGTTCTGTTCCCCCC | 388795 |
rs771725615 | snp | C/T | 0.000205044 | 0.0101232 | missense | EFCAB8 | GRCh38.p7 | 20:32959912 | TGGCCCTGATGTCCC[C/T]GTGGGCCGGAGAGCG | 388795 |
rs771772884 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901835 | TGGGATTACAGGCAC[A/G]CGCCATCATGCCCGG | 388795 |
rs771778459 | in-del | -/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877505 | TGAGCCATTGCACTT[-/G]GCGGTTTTTATTTCT | 388795 |
rs771804546 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928304 | ACAATGGCACGATCT[C/G]GGCTCACTGCACCCT | 388795 |
rs771822297 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932234 | ATACAAAAATCAGCT[A/G]GGTGTGGCGGTGCAC | 388795 |
rs771831013 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863329 | TGCTCTCCCGAAGTC[C/T]TGGCTTGCAAGGGCA | 388795 |
rs771902017 | snp | C/G | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859801 | CATAACCACAATACA[C/G]TTATCAAAAGCAGAA | 388795 |
rs771918253 | snp | C/T | 8.82184e-05 | 0.00664089 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32961195 | GCCGACTCAGCAGCC[C/T]GACTTCCTGACCAGC | 388795 |
rs771952574 | in-del | -/TC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960846 | GGGCCTCACCCAGGG[-/TC]CAGCTCGAGGCCTCA | 388795 |
rs771964283 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942200 | AATGTCCTAAGTGAG[A/C]AAAACATTTTTGGTT | 388795 |
rs771965078 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920809 | GGAAGTGAGCAGTGT[A/C]CCCTCTGGATTGGGG | 388795 |
rs772020884 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897796 | TCGGTGCCTTCATTG[A/C]GACAGATGCTTGGTG | 388795 |
rs772028691 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870198 | TTTGTGTCTGGTCTG[A/T]AGATAGGGTGATTCC | 388795 |
rs772125066 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909497 | CCTGGGGCAAGGGGG[A/C]GGCAGGGAGGGCTTC | 388795 |
rs772143739 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908529 | TGGGACTGCTGAAGC[A/G]GCTAGACTCTGTGGC | 388795 |
rs772167238 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866384 | CTCAGGTCATCTAAT[C/T]ATCCACGTTAGAGTC | 388795 |
rs772222733 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895164 | GGTGCTGGCTCTACT[C/T]GTCTGTGTCAGACTG | 388795 |
rs772224527 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952109 | CTACAAAAAAAAATA[C/T]TAAAAATTAGCCAGT | 388795 |
rs772254472 | snp | C/T | 8.75235e-05 | 0.00661469 | missense | EFCAB8 | GRCh38.p7 | 20:32930518 | CTGCTGGGGAAGTTC[C/T]CTGTGGACCTAGACA | 388795 |
rs772301084 | in-del | -/ACTT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933452 | CATATCTACCACCTC[-/ACTT]ACAATTTTTATGGTG | 388795 |
rs772341622 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912356 | TGAGGCAGGACAAGC[C/T]GGGAGGTGGAGGCTG | 388795 |
rs772364680 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946645 | TTTTAAAAATCAGAT[G/T]TCTGAAGTATAATTT | 388795 |
rs772438433 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32912009 | AGTGGGATCAGTTAA[G/T]TCACAGCCACCCATG | 388795 |
rs772458128 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960876 | CATTCTCAGAAGCGG[G/T]CAGTCTGCTCGCCAG | 388795 |
rs772462424 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958346 | GCTGACCCTTGAAGG[G/T]AGAGGATAAGGGGCA | 388795 |
rs772470051 | snp | A/G | 0.000185874 | 0.00963858 | missense | EFCAB8 | GRCh38.p7 | 20:32892287 | AGCTGTGCTCTGGTC[A/G]TGGACTACTGGTGAG | 388795 |
rs772503428 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895948 | GGATTACAGGTGTGA[A/G]CCACTGCGCCTGGCC | 388795 |
rs772523549 | in-del | -/TGTT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905427 | CTGATGGCAGTAAAC[-/TGTT]TGTCCAGATCCCCCT | 388795 |
rs772528125 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875036 | TTACAGGCGTGAGCC[A/G]CCGTGCCTGGCCTGG | 388795 |
rs772575366 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874011 | CTGCAACCTCCGCCT[C/G]TCAGGCTCAAGCAAT | 388795 |
rs772685449 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925598 | CCTCAAGTGATCCTC[C/T]TGCCTCAGCCTCCCA | 388795 |
rs772703402 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919577 | TCTTCGCTCAGTGCA[A/G]CCTCTGTCTCCTGGG | 388795 |
rs772780123 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947084 | GATTATGAATGAAGC[C/T]GCTTTAAACATTGTT | 388795 |
rs772787044 | snp | A/G | 8.86407e-05 | 0.00665676 | missense | EFCAB8 | GRCh38.p7 | 20:32961214 | TTCCTGACCAGCAGG[A/G]GCCCAGACCAGCAAG | 388795 |
rs772806510 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863367 | GTGGGTGGGGAGGGT[A/T]TATGCAGTGGAAATG | 388795 |
rs772811255 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881657 | TTTGCAAGGGACATC[A/G]GGTTCAGCCACTGTG | 388795 |
rs772847524 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954058 | TGATACACCTGCCTC[A/G]GCCTCCCAAAGTGCT | 388795 |
rs772851239 | snp | C/G | 8.84995e-05 | 0.00665146 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878816 | TCCCCCTGTAAGGAG[C/G]CTCTTCCTGGGCCTT | 388795 |
rs772864308 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891972 | GTGCTGGGATCATGG[G/T]CATGAGCCACTGCAC | 388795 |
rs772876518 | snp | A/G | 9.26484e-05 | 0.00680556 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906520 | CGCTCTCTTGGGGCC[A/G]CTGCTCCCGGCCCTG | 388795 |
rs772882539 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933431 | TGATTAAATCAAGCC[A/G]ATTAACATATCTACC | 388795 |
rs772922952 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877628 | CATTCTCAGGGCTTT[A/G]CCCAGTGGTCCTTGT | 388795 |
rs772979488 | snp | C/G | 0.000376683 | 0.0137186 | missense | EFCAB8 | GRCh38.p7 | 20:32960078 | GTGAGCAAAGTCTTG[C/G]GAGCGGCGTATAAGC | 388795 |
rs772979924 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928976 | TTTTTTGTGAAGGTG[G/T]TATATTTATTGATTT | 388795 |
rs772983114 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942256 | TTGATTTTAATTAAG[A/G]TGCCTTTGTTTATTA | 388795 |
rs772997332 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865319 | TGTGTATGGGAGACA[-/C]CACGTGAGTAAGCAC | 388795 |
rs773002499 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928309 | GGCACGATCTCGGCT[C/T]ACTGCACCCTCTGCC | 388795 |
rs773043025 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887757 | CTCACATTCTGTCTG[A/T]GCACATGCTACACGA | 388795 |
rs773065168 | snp | A/G | | | missense | EFCAB8 | GRCh38.p7 | 20:32943784 | ACGTCAAGGCTTGGA[A/G]ACTCTCCGGTGATGC | 388795 |
rs773094246 | snp | A/G | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860701 | TTTATAAAAATTGGC[A/G]TCATAGTGTGCACCC | 388795 |
rs773178936 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897797 | CGGTGCCTTCATTGC[A/G]ACAGATGCTTGGTGA | 388795 |
rs773245686 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959524 | CAGATAAAGCCAGAT[C/T]GGGTGTCAGGTCTGC | 388795 |
rs773254767 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867835 | GGAGGGTTCAGACAT[A/C]ATAAGCATTTTTTTT | 388795 |
rs773257077 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952202 | CCCGGGAGGTTGAAG[A/G]TGCAGTAATCTGTGA | 388795 |
rs773257990 | snp | C/T | 0.000104948 | 0.00724314 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32920262 | GAGCTGGGGAGTGGG[C/T]GGTCAGGATTGGGTG | 388795 |
rs773275339 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936613 | TTTGTCAAAAATCAA[C/T]TGACTATTAGTGCAT | 388795 |
rs773301073 | in-del | A/GACTCCGTCTC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899394 | TGGGGGACACAGTGA[A/GACTCCGTCTC]AAAAAAAAAAAAAAA | 388795 |
rs773370832 | snp | C/T | 9.34885e-05 | 0.00683634 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892318 | TCTCCACTGGGTGTT[C/T]CTCACATGAACCAGG | 388795 |
rs773388348 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905824 | GGCACCTATGGAATC[A/G]GTGTTCTATGACCTG | 388795 |
rs773395716 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928512 | AGTGCTGGGATTACA[A/G]GCATGAGCCACCGCA | 388795 |
rs773428973 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932267 | CTGTAATCCCAGCTA[C/T]TTGGGAGGCTGAGGC | 388795 |
rs773450120 | in-del | -/CTGTGGCCT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890244 | CTCCTCTGGTAGGTG[-/CTGTGGCCT]GGGTCTCTGTGCTCT | 388795 |
rs773468956 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956207 | TTCCTGTACAAGAAT[C/T]TTACATCCCTCCCAT | 388795 |
rs773472274 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913490 | AGCAAAATTCAGTCT[A/G]TGGCATTCCGTCCCT | 388795 |
rs773493768 | snp | C/T | 8.70511e-05 | 0.00659682 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32930532 | CCCTGTGGACCTAGA[C/T]AATGGGGATGTTGTC | 388795 |
rs773518836 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936292 | GCCTGACTCAGCCTC[C/T]CAAAGTGCTGGGATT | 388795 |
rs773529546 | snp | A/G | 9.18653e-05 | 0.00677674 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32917355 | GCAGACCTACCACAC[A/G]GAGGACATCCTGAGC | 388795 |
rs773637072 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879694 | AAGCGTAATACATGG[C/T]GGAAATAGCAAGGAC | 388795 |
rs773650596 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900727 | GTGCGCCACCATGCC[C/T]GGTTAATTTTTTTTC | 388795 |
rs773650687 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32903606 | TCCAGAACATTTTTC[A/G]GCAGCACATATACGT | 388795 |
rs773661256 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960981 | CATGGGCCCGCAGGC[A/C]ACGGTGGTTAGTGGT | 388795 |
rs773675526 | in-del | -/CCTCACATGAACCAGGAGGCCCAGG | 9.3471e-05 | 0.0068357 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892318 | TCTCCACTGGGTGTT[-/CCTCACATGAACCAGGAGGCCCAGG]CCTCCTGCAGCAGCC | 388795 |
rs773717806 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874076 | CAGGCATGTGCCACC[A/G]TGCCTGGCTAATTTT | 388795 |
rs773772927 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885910 | GGTGTCCCTTTAGCT[A/G]TCCCTGCCCACCAGG | 388795 |
rs773900631 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925599 | CTCAAGTGATCCTCC[G/T]GCCTCAGCCTCCCAA | 388795 |
rs773924538 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932108 | GGTGGGCCGGGCACG[A/G]TGGCTCATGCCTGTA | 388795 |
rs773963711 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916778 | ATATTCAGTGCTGTG[-/A]AAAAAAAAGTAGGAG | 388795 |
rs773990721 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919448 | ACACCACTGTTTTCA[A/G]ATCTTCTAGGGAAAT | 388795 |
rs773994686 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862284 | TATAGGCATGTGCCA[C/T]CACACCTGGCTAATT | 388795 |
rs774010280 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883485 | GGTTCCCATGTAGCA[C/T]GTCCAGTTCATATAG | 388795 |
rs774013299 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946577 | TGTATCTTTCAAAGA[C/T]GTCTTTGACTATCCC | 388795 |
rs774038638 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895073 | TCCCTGGGAGGGAAC[C/T]TGAGCCTAGACTGCC | 388795 |
rs774043139 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900591 | TTGTTTTTTTGTGAC[A/G]GAGTCTCACTGTGTT | 388795 |
rs774056826 | snp | A/C/T | 0.000179296 | 0.00946688 | synonymous-codon, missense | EFCAB8 | GRCh38.p7 | 20:32896519 | TTGCATAGAAGCTAC[A/C/T]GGCTGAAGGTGAGTT | 388795 |
rs774101196 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944483 | AAAAAATAATAATAA[A/T]AATAAAGTGACTTAT | 388795 |
rs774102805 | snp | A/G | | | missense | EFCAB8 | GRCh38.p7 | 20:32930567 | GTGCCATGGCCACTG[A/G]TAAAAATGACTGGAT | 388795 |
rs774107627 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869385 | GGATTACTGGTATGT[A/G]CCACCACGCCTGGCT | 388795 |
rs774115700 | snp | A/G | 8.80165e-05 | 0.00663329 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876053 | CACCTGGGTGAGGAG[A/G]GTGCCCCTGCTTCCT | 388795 |
rs774155392 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918806 | AGGGCATGGCTAATA[C/G]CAGCCCTAAAAGTCT | 388795 |
rs774156844 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881495 | AGCCACCGCATCCAG[C/T]CAGTCATCTCTTGCT | 388795 |
rs774164468 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870105 | CTTTTGAGATTTACA[A/G]CCACACTGTGATGTG | 388795 |
rs774178985 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925803 | GGGACCCACAGGGAG[A/G]CCATTAACCCGCTGT | 388795 |
rs774209150 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873540 | CTTTTCCTTCAGCCA[A/G]AGTTTATATTTTGAT | 388795 |
rs774226676 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954006 | AGACAGAGTTTCATC[A/T]CTTTGGCCAGGCTGG | 388795 |
rs774315610 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908509 | TGGCCACGTCCTGTC[C/T]CTCCTGGGACTGCTG | 388795 |
rs774320646 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904902 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCTACTG | 388795 |
rs774323322 | snp | C/T | | | missense | EFCAB8 | GRCh38.p7 | 20:32931320 | TCCCACACTACATTC[C/T]CTTGGAGGATAAAGA | 388795 |
rs774348087 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868117 | ATTGCTTTTGCACCA[A/G]TGTGATATGTGGTCC | 388795 |
rs774389667 | snp | A/G | 9.23233e-05 | 0.00679361 | missense | EFCAB8 | GRCh38.p7 | 20:32885510 | CCTCCCACAGGAACC[A/G]TGGCTGTGAGGTGGT | 388795 |
rs774424839 | in-del | -/AT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867513 | GTCTCTCTTTAAATC[-/AT]GTGCTGAAAATGTTT | 388795 |
rs774425507 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906021 | TGTCTCTATCCCTAG[C/T]GCAGGGCAGTTCTAT | 388795 |
rs774499992 | snp | C/T | 9.37603e-05 | 0.00684626 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898652 | CTCTCCTGGCTAAGG[C/T]GGTGGGGCTGGAAGG | 388795 |
rs774509577 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911826 | TGTTCATCATAGTCA[A/G]GTGGCCTGGCTTCAA | 388795 |
rs774523794 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928331 | CCCTCTGCCTCCCAG[A/G]TTCAAGTGATTTTCC | 388795 |
rs774554540 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945426 | TTCCCAAAGTGTTGG[A/G]ATTATAGGTGTGGGC | 388795 |
rs774559140 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936109 | GCAATCTCAGCTCAC[G/T]GCAACCTCTGCCTCC | 388795 |
rs774579263 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951211 | TGAAAGCATATGCCC[A/G]GGTAAAGACTACATA | 388795 |
rs774605263 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32957230 | ACTCCAATGTGAATC[-/T]TCTGGAGGGCCCACT | 388795 |
rs774621598 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892308 | TACTGGTGAGTCTCC[A/C]CTGGGTGTTCCTCAC | 388795 |
rs774669178 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949936 | ACCTGGGAGGCGGAG[A/G]CTGCAGTGAGCCAAG | 388795 |
rs774698756 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955359 | AGCATGGGCAACAAT[A/G]TGAGACCCTGTCTCT | 388795 |
rs774730052 | in-del | -/AAA | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890001 | GAGAGACTCAGTCTT[-/AAA]AAAAAAAAAAAAAAA | 388795 |
rs774767897 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959220 | GCAAACTCATGGCTG[C/T]AATTTTATGTGATAA | 388795 |
rs774834834 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872827 | CCGGGTGCAGTGGCT[C/T]ATGCCTGTAATCCCA | 388795 |
rs774878695 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897137 | TACCTGTATTCCCCC[-/T]ATCTACTTCCTGTGG | 388795 |
rs774932153 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895158 | CCTGACGGTGCTGGC[G/T]CTACTCGTCTGTGTC | 388795 |
rs774995810 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32881883 | GGGAATTCTGACAAC[A/G]TTTTAAAACATGGTG | 388795 |
rs775008821 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32883896 | GGGTTTCACCACGTT[A/G]GCCGGGCTGGTCTTG | 388795 |
rs775066550 | snp | C/T | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860837 | TCAAACTTCTGGATG[C/T]AGGTAATCCTCCCAT | 388795 |
rs775088813 | in-del | -/CTCT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939204 | TTCTTTCTTTCTTTC[-/CTCT]CTCTCTCTCTCTCTC | 388795 |
rs775105217 | snp | A/T | 9.21786e-05 | 0.00678829 | missense | EFCAB8 | GRCh38.p7 | 20:32867693 | CAGCTGTTTACTGAG[A/T]TACACCTGGCCAAGA | 388795 |
rs775141323 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945212 | CACCCAGGGTTGAGT[A/G]CAGTGGCACGAATTC | 388795 |
rs775142315 | in-del | -/CTATCT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938503 | GGAGGAAGAAGTTAA[-/CTATCT]CTATCTGCAGATGAC | 388795 |
rs775158692 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872600 | AGGGTTCGAGACCAG[C/T]CTGGCCAACATGGTG | 388795 |
rs775169647 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906831 | GGACTGACACCCACG[C/T]CTTGACCACAGTGAC | 388795 |
rs775177875 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913017 | TCTGCTCATCCATCC[A/G]TTTATTCATTATTCA | 388795 |
rs775192384 | snp | A/G | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859383 | GAGTTTTACATCTCA[A/G]CCTTCCCTTCCTTCC | 388795 |
rs775192982 | snp | A/G | 7.74803e-05 | 0.00622368 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863751 | GTCCTTACAACGACT[A/G]GAGTTAAGTTGACTA | 388795 |
rs775237765 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944147 | TGAATTTTGAGAAAG[G/T]AAATACATACCCATA | 388795 |
rs775296585 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916521 | TCCTTGGCCCCTCAA[A/G]GTGCTGGGATTATAG | 388795 |
rs775327586 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918036 | TCCCCCAGAATAGCT[C/T]AGCTTTTTATCTGTT | 388795 |
rs775328460 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952548 | AAAATCAATTTGTTA[C/T]TGGCCACTCATACAT | 388795 |
rs775329569 | snp | A/G/T | 0.000181509 | 0.00952511 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893133 | GGTGTGAGCCACCGC[A/G/T]CCCAGCCCACACAAC | 388795 |
rs775352556 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884627 | GGTCAGACCAGGCCT[A/T]CCGGATTTGGAAAGG | 388795 |
rs775376238 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919177 | CAGTGAGTACAGTAT[C/T]CCAACAATCAGTGCA | 388795 |
rs775376503 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908492 | ATGGGACACCCAAGG[A/G]GTGGCCACGTCCTGT | 388795 |
rs775395297 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867931 | AGCCTCAACCTCCCA[C/T]GCTCAAGCGATCCTC | 388795 |
rs775403775 | snp | G/T | 8.89957e-05 | 0.00667008 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930634 | GAGGAAGAACTGGCA[G/T]GAAGATTGAGGGGCT | 388795 |
rs775450436 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915374 | TCTCAAAACACTAGA[A/G]CACAAATATAATTCA | 388795 |
rs775503512 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948475 | ACTTCCCAACTCATG[A/C]GGCAACTTGGTACCA | 388795 |
rs775524068 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879840 | TCCTTTAGTTTAACA[G/T]ACTCAGTATGCTGCG | 388795 |
rs775532010 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887529 | CCAGTGAGCCGAGAT[C/T]GCACCACTGTGCTCT | 388795 |
rs775570107 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916558 | GCCACCATGCCTAGC[C/G]TAGGACCTCTTTTAT | 388795 |
rs775573347 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32878099 | GGCGAAACCCCATCT[C/T]TACAAAAAATACAAA | 388795 |
rs775595503 | in-del | -/G | 9.27343e-05 | 0.00680871 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918338 | CATTGCAGTGCCTTA[-/G]GGGCTGCTTTCTTCT | 388795 |
rs775613910 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928172 | GACACTATTGTCAAT[G/T]GAATTATTTTTGTAA | 388795 |
rs775621401 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949741 | TGATGGTTCACACCC[A/G]TAATCCAAGCACTTT | 388795 |
rs775681415 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956906 | CTATATGTATACTAG[A/G]CTATTTGACTTTGTC | 388795 |
rs775688261 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32888432 | GGTTTCAACATTGGC[C/T]AGGCTGGTCTCGAAC | 388795 |
rs775728265 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936079 | GCTCTGTCACCCAGG[C/T]TGGAGTGCAGTGGTG | 388795 |
rs775910348 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952708 | TGAGTACTTTTATCA[C/G]TGTATCACTTGCCCG | 388795 |
rs775944542 | snp | C/T | | | missense | EFCAB8 | GRCh38.p7 | 20:32918551 | CCGAGAGACAAGGAG[C/T]CAGACAGGCCTGTGC | 388795 |
rs775983812 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943873 | CTGTCTGAACATAAG[C/T]TGGTATGAACTTTGT | 388795 |
rs776010689 | snp | C/T | 0.000273386 | 0.0116884 | missense | EFCAB8 | GRCh38.p7 | 20:32878726 | ATGTGGATTACATGA[C/T]GCGTGAGTTCCAGGG | 388795 |
rs776030119 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882948 | GATCTGCCCGCCTCG[A/G]CCTCCCAAAGTGCTG | 388795 |
rs776043809 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865089 | TGGGGCTCTGCAGCC[A/G]TGTGCTTCCCCTCAT | 388795 |
rs776104724 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894207 | CCAGGGGCCCCATGC[A/G]GGGCCACCAACCCCC | 388795 |
rs776153591 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882885 | CATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 388795 |
rs776199897 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32897868 | AGCACCAAAGAAATA[G/T]TTGATGAGCCAATCT | 388795 |
rs776208644 | snp | A/G | 0.000157878 | 0.00888336 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32911740 | ATTACAGCCAGGGAC[A/G]GCCTCTTGGGAAGCA | 388795 |
rs776228296 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909626 | GGAAGGCTCAGTCTC[A/G]GGGAGCGGGGGCCAT | 388795 |
rs776273442 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32942572 | AACTGATTGTCTATC[A/G]TATGGATTACAAATA | 388795 |
rs776306759 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921435 | TGCCCATGCTGGTCT[C/T]GAACTCCTGGGCTCA | 388795 |
rs776335924 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879808 | ACAGTCCTTCCTGAA[C/T]ATACTGCTTCTCAAA | 388795 |
rs776428166 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917179 | CTTCAGCCCAGCTCC[A/G]ACACCTGAGAGTATC | 388795 |
rs776456125 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951256 | GCAGTATTTTTTTGT[G/T]ACAGCCTCAAACTAG | 388795 |
rs776481497 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917933 | AAGCAGGAAGGGACC[G/T]TAGGGGCCGCCTCAT | 388795 |
rs776489267 | snp | C/T | | | missense | EFCAB8 | GRCh38.p7 | 20:32898578 | CCATCGAGAAGTCCT[C/T]TCTGGTGCTGACAAT | 388795 |
rs776503766 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930161 | GCACCATTGTGGTTA[C/T]TAAGGACAAAGTAGT | 388795 |
rs776536973 | snp | C/G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949288 | TGCTGAGACAAAGTA[C/G/T]AGAAGATTTACTGTT | 388795 |
rs776547654 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877989 | TCAGGATTCAAGAAC[A/G]GGTCTGCTGTCCAAG | 388795 |
rs776549628 | in-del | -/TTC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936421 | CCTTTCCTCTAGGTA[-/TTC]TTCTAGTTGTTTTAC | 388795 |
rs776565918 | snp | A/G | 8.66514e-05 | 0.00658165 | missense | EFCAB8 | GRCh38.p7 | 20:32930560 | GTCGTGGGTGCCATG[A/G]CCACTGATAAAAATG | 388795 |
rs776670694 | snp | A/G | | | missense | EFCAB8 | GRCh38.p7 | 20:32889376 | CACAATATGAACCTC[A/G]TTGCAGTTGCGTCTA | 388795 |
rs776673215 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886487 | GGGCTTTCTGAGCCT[A/G]TGTAACTGCAGAGTG | 388795 |
rs776682794 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939763 | GCAGTGGCGCCACCT[C/T]GGTTCACTGCAACCT | 388795 |
rs776721207 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887916 | CAGGTGACATCTGCA[C/G]ATGGAAAATAGGATT | 388795 |
rs776738095 | snp | A/G | | | downstream-variant-500B | EFCAB8 | GRCh38.p7 | 20:32962106 | ACCTTGTTCTGTCCC[A/G]TGTGCAGAGAGGGCT | 388795 |
rs776754733 | in-del | -/C | 0.00010158 | 0.00712597 | frameshift-variant | EFCAB8 | GRCh38.p7 | 20:32906880 | CATCCGCCTGTGGAA[-/C]CCCTTTGTCTCAAAG | 388795 |
rs776763906 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910841 | CTTCCGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 388795 |
rs776784073 | snp | C/G/T | 0.00119804 | 0.0244471 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32896406 | GCTTTGCTTGCCAAG[C/G/T]GAAGGGGGAAAGCTG | 388795 |
rs776793770 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885940 | GTTTCCTTCTCTTGC[A/G]TCCCCATCTCAGTGA | 388795 |
rs776797697 | in-del | -/CCA | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32909052 | AGGCTGAGCCACAAC[-/CCA]CAGATGGGAGCAGAA | 388795 |
rs776801897 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906154 | CTCCCTTGGAACCCC[A/G]CTTTTTTCTTGATTT | 388795 |
rs776815270 | in-del | -/AAAG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948528 | AAGAAAGTGAAAAAG[-/AAAG]AAAGAAAGAAAGAAA | 388795 |
rs776861860 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949524 | GCCATGGTAATCAAG[A/G]CAGTGTGGTAATGGC | 388795 |
rs776875632 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924774 | AATTGCATGCAAAAG[A/G]TTGAATGTCTATTGG | 388795 |
rs776890867 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864855 | ACTATGAGACAAGGA[A/G]TAATAACAAGAGCTG | 388795 |
rs776937676 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931753 | ACAGAGCAAGACTTC[A/G]TTTCAAAAAAGAAAA | 388795 |
rs776971828 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934664 | TTGAATCGTGGGGGT[A/G]GGTTTTTCCCACCAT | 388795 |
rs777002568 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908243 | ATCCCCGAGACCCAT[G/T]CTCAGCGTCTTGCCT | 388795 |
rs777052739 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869063 | ACTTCCAAGCTCACT[C/T]AGGTTGTTGGCAGAA | 388795 |
rs777094275 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892100 | GTTGCCATGGGGGAA[A/G]AAGGGCTGAAGGGGC | 388795 |
rs777095055 | in-del | -/AGAC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949544 | GTGGTAATGGCATAG[-/AGAC]AGACAGACAGATCAA | 388795 |
rs777116261 | snp | C/T | 0.000177936 | 0.0094306 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32917427 | CAGTGGGGACATCCT[C/T]TTCTGGAACACCGGC | 388795 |
rs777149403 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948277 | CTACTAAATCTTACA[C/G]AAGAAGAAACAGATA | 388795 |
rs777162592 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934553 | CTATTTCTCGTAGTG[A/G]TTGATATGGTTTGGT | 388795 |
rs777166918 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902934 | CCCCGGCGTCTCCCC[A/G]ACTGTCCCCTCTTCC | 388795 |
rs777224046 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876782 | GACCAGCCTGGGTAA[C/T]GTGGTAAAACCCTGT | 388795 |
rs777226322 | snp | A/G | 8.97304e-05 | 0.00669755 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876089 | GCTGGAGGGAGGCTG[A/G]AGGGTCCAGTCCTTG | 388795 |
rs777251105 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32919330 | GCTAGGCATAGGGCA[A/G]TCTAGACCTAAATCC | 388795 |
rs777301532 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865602 | CAGGAGTTCGAGGCC[A/T]GCCTGGTCAACATGG | 388795 |
rs777335395 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935656 | GGATTACAGGCATGC[A/G]CCACCACGCCCAACT | 388795 |
rs777362547 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949204 | AAATTGAAGTAAAAG[A/G]TACATTTACGAAAAC | 388795 |
rs777375132 | snp | A/G | 0.000184502 | 0.00960296 | missense | EFCAB8 | GRCh38.p7 | 20:32911625 | GGTGCCTGCTCACAG[A/G]TTTGCGGGATGGCAC | 388795 |
rs777418669 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944590 | ATGCTTTCATGTTCC[G/T]GCCTAGCATCCTTTT | 388795 |
rs777434874 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958197 | GGCAGGATGCTTTAG[A/G]CCTGAGCTCCGAGTG | 388795 |
rs777464363 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923818 | CATGTCCTGGGTACA[C/T]TGCACAGAGTCTGTA | 388795 |
rs777470724 | in-del | -/CCCCCCCCTC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32929464 | TTTCTCCCTTCCCTC[-/CCCCCCCCTC]CCCTCCCCTCCCCTC | 388795 |
rs777470871 | in-del | -/GCC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894087 | AGGATACGGCTCAGG[-/GCC]GCCTAGGGAACTCAT | 388795 |
rs777544913 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885663 | GGGCCCCTACACATG[A/G]TGCACACATGGGTGA | 388795 |
rs777558852 | snp | A/G | 0.000115042 | 0.00758338 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917281 | GCTCTCAGCCCTCCT[A/G]CCTCTGGCCATATGC | 388795 |
rs777569978 | in-del | -/TTG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954371 | TTTTCCCAAAACCAT[-/TTG]TTGTTGTAGAGACTA | 388795 |
rs777626884 | snp | C/T | 9.45046e-05 | 0.00687338 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885676 | TGGTGCACACATGGG[C/T]GATTGGAGAGCCTCT | 388795 |
rs777627259 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916354 | CCTTGAACTCCTGGG[C/G]TCAAGTGATCCTCCT | 388795 |
rs777631699 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32884255 | TACTGAGCCTGGGCC[A/G]GGTGCACCAAATGCA | 388795 |
rs777655502 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898411 | GGGCACCTCCAGTCC[C/G]AGCACCTGGTCATGT | 388795 |
rs777772496 | snp | C/T | | | missense | EFCAB8 | GRCh38.p7 | 20:32908318 | ACATATGCCTCCAGT[C/T]CTTCTGTGGGAAGTT | 388795 |
rs777831103 | snp | A/G | 0.00018423 | 0.00959589 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32911695 | GACCTTTCCCAGTCC[A/G]GAACAGCTGGAGGTC | 388795 |
rs777834874 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894737 | CCTGATAGCTTTGGT[A/G]TAAGAAACGTGGAAC | 388795 |
rs777911684 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32953614 | TGTGCTTGTTGGCCA[C/T]TGTATATCATCTTTG | 388795 |
rs777940890 | in-del | -/AGAT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908879 | GGGAAACTGAGTCAC[-/AGAT]AGGAAGGCCATCTGT | 388795 |
rs777960940 | in-del | -/TTCTTTCTTTCC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939193 | TCTTTCTTTCTTTCT[-/TTCTTTCTTTCC]TCTCTCTCTCTCTCT | 388795 |
rs778095137 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886425 | GGAAAGCACTGCTCT[C/T]CAGGGCTCTACAGAA | 388795 |
rs778113044 | snp | G/T | 9.29239e-05 | 0.00681566 | missense | EFCAB8 | GRCh38.p7 | 20:32893296 | CCAGGGCCTCCAAGT[G/T]GGGTAGCTAAGATGC | 388795 |
rs778140091 | snp | C/G | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859432 | GGTACTTGTCTTGGC[C/G]TCTCCCCTCTTGCTT | 388795 |
rs778169175 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32887082 | AACCACCTGGGGAGC[C/T]CGAGAGCGCAGTCCT | 388795 |
rs778176523 | snp | A/C | | | downstream-variant-500B | EFCAB8 | GRCh38.p7 | 20:32961915 | ATCCCCTGGCCCTGG[A/C]AGAGGCAGAGAGGAG | 388795 |
rs778186884 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941360 | ACCATATTACCCAAC[A/T]GTTCCACTCCCAAGT | 388795 |
rs778193232 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869749 | GTGTATGTTTTCATA[C/T]GTCTTTAATCATACT | 388795 |
rs778208702 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891533 | TAGAACCCCATTTTA[A/G]AGATAATTATGTCAT | 388795 |
rs778208915 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32915659 | GACCATCCATCCTCT[-/A]ACCTATTACCTACTT | 388795 |
rs778218748 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32914968 | TAGTCATGCGATTAT[C/T]GCTCACTGCAGCCTC | 388795 |
rs778220641 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928640 | CGTTTTCTACATATA[A/G]GATAATATCATCTGC | 388795 |
rs778299426 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947749 | GCCTATATTAGAAGG[A/G]AAAAAGTTCAAATCT | 388795 |
rs778318858 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32873029 | CCCAGGATGCGGAGG[-/T]TTGCAGTGAGCCGAG | 388795 |
rs778349122 | in-del | -/TGAC | | | frameshift-variant | EFCAB8 | GRCh38.p7 | 20:32906843 | ACGTCTTGACCACAG[-/TGAC]TGGTGGCTACGATGC | 388795 |
rs778429829 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901651 | GCCTTTGCACAGCTC[C/T]GCTGTCTGTGGTATG | 388795 |
rs778446887 | in-del | -/GA | 8.97868e-05 | 0.00669965 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876088 | GCTGGAGGGAGGCTG[-/GA]GAGGGTCCAGTCCTT | 388795 |
rs778481873 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32949133 | ACAAGGTTGCAGGAT[A/G]CAAGATCAATACAAA | 388795 |
rs778512418 | snp | G/T | 9.22977e-05 | 0.00679267 | missense | EFCAB8 | GRCh38.p7 | 20:32918363 | TCTTCTTGGTACAGG[G/T]GCAAGATGTGAACAA | 388795 |
rs778537082 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905308 | GTTTCATGTGACATG[C/G]GAGCCTTCAGAAAAA | 388795 |
rs778561279 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32956201 | TGCTGCTTCCTGTAC[A/G]AGAATCTTACATCCC | 388795 |
rs778580855 | snp | A/G | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32859365 | CAATTCTAAATATCA[A/G]CCGAGTTTTACATCT | 388795 |
rs778594934 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32875829 | TGTGGTCTTCAGTGT[A/G]TCCCCCTCAGCACCC | 388795 |
rs778622518 | in-del | -/TCT | | | cds-indel | EFCAB8 | GRCh38.p7 | 20:32961764 | TCACCTGTCTCCTAA[-/TCT]TGTCTTCTCTCTGGC | 388795 |
rs778647934 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874870 | TCCTGCCTCAACCTC[C/T]CAAGTAGCTGGGATT | 388795 |
rs778678286 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913452 | TCGCCTTAGGGATTA[C/T]GTTTCAATATATGAA | 388795 |
rs778745484 | snp | C/T | | | | | GRCh38.p7 | 20:32919995 | GGGAGTGCCGCTCTT[C/T]TATCATCTTCCTCTG | 388795 |
rs778772824 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886328 | TGCCAGCTCTTGGCT[A/G]AGAGTAGTAAGTGAG | 388795 |
rs778773011 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32893595 | CATGATGCCAGTGGT[A/G]GGACCCTGGGGAAGT | 388795 |
rs778778550 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948956 | TAAGACATGTCACTT[C/T]GATTCAAAATTATAC | 388795 |
rs778795388 | in-del | -/CTTC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32866728 | CCTGGGGTTTTCTTC[-/CTTC]CTTCCTTCCTTCCTT | 388795 |
rs778857874 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882547 | TATTTTTGAGACAAG[G/T]TCTTGCTCTGTGGCC | 388795 |
rs778901977 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918838 | AAAGCTGAAAGGCAG[G/T]ACCCAAAGAGAACAC | 388795 |
rs778946040 | snp | A/G | 8.79082e-05 | 0.00662921 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32961183 | CAGTGATCTGATGCC[A/G]ACTCAGCAGCCTGAC | 388795 |
rs778950257 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934342 | CCACATTTGCATTAT[C/T]CATTCATCCACTGAT | 388795 |
rs778976913 | snp | A/G | 0.000202388 | 0.0100575 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906796 | CACCAGTGGGTGAAG[A/G]TCCCCAGTGGAGGCC | 388795 |
rs779006554 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32889118 | TTTACGAATGTGGAA[A/G]CTGAGACCCAGGGAG | 388795 |
rs779055855 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861284 | ACCCACTCCACTGAA[A/G]CACATTTTATTTTAT | 388795 |
rs779147553 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930104 | ATCAAACTTGTAAGC[C/G]TTCATTTGATAAACA | 388795 |
rs779224037 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32868886 | GCTACTTGGGAGGCT[A/G]AGGCAAGAGAATCGC | 388795 |
rs779230473 | in-del | -/TCTTTCTTTCTT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939126 | TTCTCTCTTTCTTTC[-/TCTTTCTTTCTT]TCTTTCTTTCTTTCT | 388795 |
rs779237418 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32945836 | ACGCATGTAAATTCG[C/G]AATTACAGGAATCTA | 388795 |
rs779246432 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895869 | AGCCACCGTGCCTGG[C/T]CCAGGCTGGTCTCTT | 388795 |
rs779276598 | snp | A/G | 8.99807e-05 | 0.00670688 | missense | EFCAB8 | GRCh38.p7 | 20:32930489 | ACGCCTGGTCCCTCC[A/G]TGAGAATGGAGGCCT | 388795 |
rs779283802 | in-del | -/ATA | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933008 | GATACAATCATCATC[-/ATA]ATAATATTTATTTAC | 388795 |
rs779292575 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895837 | CGCCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 388795 |
rs779333128 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32925570 | GTTGTCCAGGCTTGT[C/T]TCGAACTCCTGGCCT | 388795 |
rs779345210 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899967 | TCTTCCTGCTGGGTG[C/G]CTCTTGCCCCTGCAG | 388795 |
rs779348592 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880592 | TAAAACAAAATTTTG[A/G]TTGGGATTTAATTGA | 388795 |
rs779398044 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885699 | GAGCCTCTGCCTTAG[C/T]ACCCCCATGGTGAAG | 388795 |
rs779417571 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941216 | GAGATCATGCCATTG[C/T]GTTCCAGTCTGGGCA | 388795 |
rs779439129 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960333 | ATGAGACTAATGTGG[C/G]CAGTTTGTTTGCCAA | 388795 |
rs779440150 | snp | C/T | | | missense | EFCAB8 | GRCh38.p7 | 20:32878795 | TCTACCTTCCCATGA[C/T]GGTCGTCCCCCTGTA | 388795 |
rs779446693 | snp | A/C | | | missense | EFCAB8 | GRCh38.p7 | 20:32908275 | TTTCCCATCCCCCAG[A/C]ATATTCGCGTGTGGG | 388795 |
rs779473465 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32930202 | GACGCAAAATCCCTG[A/C]CCTCTAGTAGTTCAT | 388795 |
rs779477765 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32904900 | CAAAGTGCTGGGATT[-/A]ACAGGCGTGAGCTAC | 388795 |
rs779478523 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32913151 | TGTCTTAGTCCATTC[A/G]GGCTGCTGTAACAGA | 388795 |
rs779569554 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32871987 | GCCTGCCCCCTGGCA[C/T]CTATCTTCTACCTGG | 388795 |
rs779620784 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938211 | ATAAAAAACAAAAGC[C/T]ATATGATTATGCCAA | 388795 |
rs779654750 | in-del | -/CCTT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939125 | TTCTCTCTTTCTTTC[-/CCTT]TCTTTCTTTCTTTCT | 388795 |
rs779675714 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886157 | GACAAGGTACTATAT[A/G]CTCCCTGTGCCTCAG | 388795 |
rs779730366 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32924025 | AGCTCTCAATATCTG[C/T]CAGACAATGAACTTA | 388795 |
rs779734782 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928073 | CATGCAAGTGGAATC[A/G]TATGTTTGTCTTTTG | 388795 |
rs779770974 | snp | A/G | 0.000265264 | 0.0115135 | missense | EFCAB8 | GRCh38.p7 | 20:32878771 | GAAAGAGCCAGTACC[A/G]CCTGCACTTCTACCT | 388795 |
rs779771830 | in-del | -/GGTAAGAAAGACAATT | 9.43619e-05 | 0.00686819 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863834 | CCCTCAACTCCAAAA[-/GGTAAGAAAGACAATT]ATCTGAACTAATAAA | 388795 |
rs779775359 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32946691 | ACCTTTTAAAAGTAT[A/G]TAGTTCTGTGAGGTT | 388795 |
rs779802258 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885659 | AGTGGGGCCCCTACA[A/C]ATGGTGCACACATGG | 388795 |
rs779852450 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32918605 | CAACCAGAAGGCTAC[C/T]CTCACTCTCTAGCCG | 388795 |
rs779862614 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862697 | CAATGGCTCGATCTC[A/G]GCTCATGGCAACCTC | 388795 |
rs779899075 | snp | A/G | 0.000375622 | 0.0136993 | missense | EFCAB8 | GRCh38.p7 | 20:32918509 | CTGAGGCGGAGCCTG[A/G]TGTCGGCTCCCCCAG | 388795 |
rs779914494 | in-del | -/CT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865786 | GGTGACAGAGTGAGA[-/CT]CTGTCTCAAAAAAAA | 388795 |
rs779927237 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32934134 | CAGGTGTGAGCCACC[A/G]TGCCCAGCCCTTTCT | 388795 |
rs779940635 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902551 | CAGGAGTTCAAGACC[A/G]GCCTGGGCAATACAG | 388795 |
rs779945733 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32886630 | ATCCTGAGGCTGTGG[C/T]TTCCATAGCCATCCA | 388795 |
rs779969554 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32954313 | TTTTGTATATGGCAT[-/A]AAAATAACAGTCCAG | 388795 |
rs780080702 | snp | A/G | 9.84204e-05 | 0.00701431 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960018 | CAGGGAGGAGTGCAG[A/G]GACCCCCAACTCGCA | 388795 |
rs780096469 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874690 | GGGATTACAGGCACA[C/T]GCCACCAAACATGGC | 388795 |
rs780102472 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32901351 | CACAAAAAAGTCTCA[C/T]AATGTTATAAGAAAG | 388795 |
rs780128612 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944545 | ATTTTTCTATGTGTT[C/T]ACATTTATCAGAAAG | 388795 |
rs780130297 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928939 | TCTGCATCAATTAAG[A/C]TGATCGTGTGGGTTT | 388795 |
rs780134861 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879064 | GCTGGCCCCAGGCCA[A/G]TAGGTAGAAAGTGGC | 388795 |
rs780150762 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32899307 | CTACTCGGGAGGCTG[A/C]GGCAGGAGAATGGTG | 388795 |
rs780178858 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32947711 | AAAAAACAGTAGTAA[C/T]GGGGAAATTTGTAGC | 388795 |
rs780253395 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872274 | CAAGCAACCACGCCT[C/T]TCTGTGCCACATTTT | 388795 |
rs780287228 | snp | C/T | 9.21362e-05 | 0.00678672 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898632 | AACCCAGGTAAGAAG[C/T]GCTTCTCTCCTGGCT | 388795 |
rs780294645 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32898328 | CTGGTCATAGGACCT[A/G]GGCTAGGATTGCGGG | 388795 |
rs780299767 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861150 | ATGCACTGATTTGTT[A/C]ATTTCTGTGTCTATA | 388795 |
rs780354552 | snp | G/T | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860697 | TTCTTTTATAAAAAT[G/T]GGCATCATAGTGTGC | 388795 |
rs780389685 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938781 | ATGAAAGAATACCCA[A/G]ATAAATGGAAATACA | 388795 |
rs780423873 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867392 | CCCTCTCCAAAGTCG[A/G]AAGAGTCTAGGTTTT | 388795 |
rs780460306 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32936748 | ATCAGGGACTGTGAT[G/T]TCTTTAGCTTTGTTC | 388795 |
rs780465600 | snp | C/T | 9.20683e-05 | 0.00678422 | missense | EFCAB8 | GRCh38.p7 | 20:32920141 | AGCAAACAGTCCATT[C/T]ACAAAGAGGATGAAA | 388795 |
rs780481096 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879267 | GGAATTGCTCCTCAA[A/G]CCCCCAGCCAGGCCC | 388795 |
rs780481842 | snp | A/G | | | splice-donor-variant | EFCAB8 | GRCh38.p7 | 20:32917506 | TTGCAGCCCAAGAGG[A/G]TATGTTAACAGGAGC | 388795 |
rs780483726 | snp | G/T | 9.22977e-05 | 0.00679267 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32906662 | CACCCAGAAGCTGCT[G/T]GGGGGAGGGCTGCTG | 388795 |
rs780485689 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910178 | CTCCTCTGAGCCTCA[A/T]GCCCTTGGCTGAGCG | 388795 |
rs780548772 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894948 | CCCCTCCCTGGGACT[C/T]ACTTTGCAAGCTTCC | 388795 |
rs780584798 | in-del | -/TC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32944907 | AGCTTTTTGTCCCTT[-/TC]TCTCTCTCTCTGTCT | 388795 |
rs780596829 | snp | A/G | 9.34099e-05 | 0.00683346 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32930445 | GCACACGGCTGCCCT[A/G]CTGAGCAGCTGCATG | 388795 |
rs780603782 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877561 | CTTTAGAACAATGAG[A/G]CCAACTGAAAGAAAA | 388795 |
rs780609998 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32923953 | AGGATTAGAAACATA[C/T]TCCTGGAAAGCTTTT | 388795 |
rs780635401 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890003 | GAGACTCAGTCTTAA[-/A]AAAAAAAAAAAAAAA | 388795 |
rs780641316 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32867263 | AGATTTGAAATGATA[C/T]AGTTACTGAACTGAG | 388795 |
rs780722275 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32891507 | ACAGGTGTGAGCCAT[G/T]GCAGCCAGCCTAGAA | 388795 |
rs780751782 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32951474 | ACCATTTACACCTGC[A/G]TCTATTTATATAAAA | 388795 |
rs780824705 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32958301 | ACTCAACATTTGAGT[A/G]AGTGTGGGGGCTGAG | 388795 |
rs780847791 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32931714 | AGTGAGCTGAGATCG[C/T]GCCATTGCATTCCAG | 388795 |
rs780855473 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32952558 | TGTTATTGGCCACTC[A/G]TACATCTACTCCTGT | 388795 |
rs780867102 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935939 | GTGGGTTATCTCTTT[A/G]CTTTGTTCATTGTTT | 388795 |
rs780882214 | snp | C/G | 9.22807e-05 | 0.00679204 | intron-variant | EFCAB8 | GRCh38.p7 | 20:32892209 | CCTTCTGTCTTTCCC[C/G]CAGATTTCTTTGATA | 388795 |
rs780903537 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32894064 | TGCCCAGGTCGCTAG[A/G]TCCCCAGAGGATACG | 388795 |
rs780948432 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32865985 | GGATCCCAGGAATAA[G/T]TAACTGGAGGGACGG | 388795 |
rs780962390 | snp | C/T | 0.000911494 | 0.0213288 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32875939 | AGCCCTGGGCATGGA[C/T]GCCTTCATCAAGGCC | 388795 |
rs780990763 | in-del | -/CTGC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32943555 | TCCAACTGGGCTCTG[-/CTGC]CTGCAGTCCTGGGTG | 388795 |
rs780995981 | snp | A/G | 9.52336e-05 | 0.00689983 | synonymous-codon | EFCAB8 | GRCh38.p7 | 20:32917310 | GCACAGGTTCCACAA[A/G]ACCAAGCCAGTGCTC | 388795 |
rs780996409 | in-del | -/TTT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32895557 | GTCCAGACTGGTATC[-/TTT]TTTCTTTCTTTCTTT | 388795 |
rs781055731 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32905652 | GTAATCCCAGCTACT[C/G]TGGAGGCTGAAGCAG | 388795 |
rs781087603 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32902279 | AGGCCATTGCAATAG[A/T]TGAGGCTGCATAGGA | 388795 |
rs781127891 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864141 | GCCACCATGCCCAGC[-/T]AATTTTTATATTTTT | 388795 |
rs781152845 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32900241 | GATAAGGCTAATTTC[A/G]TCCAACTCCTCATTT | 388795 |
rs781154459 | snp | A/C | 0.000150978 | 0.00868712 | missense | EFCAB8 | GRCh38.p7 | 20:32959825 | ACCAGCGGCGAGAGC[A/C]GGCGGCGCTGATGGC | 388795 |
rs781155582 | snp | A/G | 9.21022e-05 | 0.00678547 | missense | EFCAB8 | GRCh38.p7 | 20:32917503 | CCCTTGCAGCCCAAG[A/G]GGGTATGTTAACAGG | 388795 |
rs781164240 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872451 | TCATGCCTGCCATCC[C/G]AGAGCTCTCAGGCTG | 388795 |
rs781245662 | snp | C/G | | | missense | EFCAB8 | GRCh38.p7 | 20:32911667 | GGAACTACAACATTG[C/G]CAAATGCCTGTTGAC | 388795 |
rs781251543 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32885441 | GGCTCTCTGTTCTGC[C/T]GCAGGTGCCCCCTCC | 388795 |
rs781266233 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32955718 | ATATCTTCTGTTCCA[C/T]GTCCTGAGCGAGGGT | 388795 |
rs781325360 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32908443 | GGAGGGAGTGGGGTC[A/G]AGGCCGCAGGTGGAG | 388795 |
rs781326049 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32927757 | TACAGTGAGCACTTG[C/G]ATAAAGTGGGGGAAA | 388795 |
rs781333377 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32882062 | AATTAGCTGGATGTG[C/G]TGGCAGGCACCTGTA | 388795 |
rs781342475 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32941738 | TAGTGACTACTGGGT[A/G]AAGAGTTTCTTTCTG | 388795 |
rs781393955 | in-del | -/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32940044 | CTTCCTTCCTTCCTT[-/C]CTTCCTTCCTTCCTT | 388795 |
rs781423471 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32935538 | TGAGATGGAGTTTTG[C/T]TCTTATTGCCCAGAC | 388795 |
rs781452447 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32870939 | TCTCGGCTCACTGCA[A/G]CCTCTGCCTCCCAGG | 388795 |
rs781453152 | snp | G/T | 9.15541e-05 | 0.00676526 | missense | EFCAB8 | GRCh38.p7 | 20:32898583 | GAGAAGTCCTCTCTG[G/T]TGCTGACAATATTGC | 388795 |
rs781505620 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32869903 | CCTCTGTTTTCAGAC[A/G]TTTAGGTTTTATTGA | 388795 |
rs781520881 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32926433 | TATTTAGCTGTTTGC[-/T]TTTTTTTTTTTTTCA | 388795 |
rs781530725 | snp | G/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921010 | CACCCCTCACTGTGA[G/T]ACTGACTCCCCGTCC | 388795 |
rs781579749 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32938124 | ACACCATGACCAAGT[A/G]AGATTTATCCCAGGA | 388795 |
rs781583058 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32876658 | TAGGAATCCTATGGG[A/G]TAGGTGCTATTACTT | 388795 |
rs781594890 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32928794 | CTTGTTCCTAATTCC[A/G]GAGGAAAAGCTTTCA | 388795 |
rs781644746 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32877149 | ATAGCTCTCCTCAGC[A/T]TAGGTATACATTCTG | 388795 |
rs781713120 | snp | A/C | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32916465 | GGTCTTGCTCTGTTG[A/C]CCAAGCTGGTCTTGA | 388795 |
rs781776552 | snp | A/T | | | upstream-variant-2KB | EFCAB8 | GRCh38.p7 | 20:32860644 | CCCGAGTAGCTGGGA[A/T]TACAGACGTCAGCCA | 388795 |
rs796068437 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32917277 | CTGAGCTCTCAGCCC[C/T]CCTGCCTCTGGCCAT | 388795 |
rs796081797 | in-del | -/TC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32922814 | TCGAGAATGAGTACT[-/TC]TCTCTCTCTCTCTGT | 388795 |
rs796084586 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933711 | TGGCCGGGCTCAGTG[A/G]CTCAAGCCTGTAATC | 388795 |
rs796124020 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32932868 | TTGCAGTCTTATGTG[C/G]CTTTTGAATCTCTAC | 388795 |
rs796172967 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32879629 | ATGCTAGGTTCAATG[A/G]AGGGTGGAAAGCTGT | 388795 |
rs796251553 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948133 | CACCAATTACCAATA[C/T]CAGGAATGAGTGAGA | 388795 |
rs796278707 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32874007 | CTCACTGCAACCTCC[A/G]CCTCTCAGGCTCAAG | 388795 |
rs796288037 | in-del | -/TT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921392 | GTGTGTGTGTGTGTG[-/TT]TTTGTAGAGATGGGG | 388795 |
rs796329152 | in-del | -/GT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921391 | TGTGTGTGTGTGTGT[-/GT]TTTTGTAGAGATGGG | 388795 |
rs796336225 | in-del | -/TTTTTTTTT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32910739 | CACCTCACTTGCTAC[-/TTTTTTTTT]TTTTTTTTTTTTTGC | 388795 |
rs796379403 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863309 | GAGCAGAGCTCTGTT[C/T]TGTCTGCTCTCCCGA | 388795 |
rs796403739 | multinucleotide-polymorphism | AGA/GGG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32939788 | AACCTCCGCCTCCCA[AGA/GGG]TCAAGCGATTCTCCT | 388795 |
rs796420943 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32863024 | CAATTTTTTTTTTTT[-/T]CCTTCTCTGCCATGA | 388795 |
rs796463534 | in-del | -/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32862135 | TTATTATTTCTTTTC[-/T]TTTTTTTTTTTTTGA | 388795 |
rs796495588 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32937558 | TAGTAATAAAATTTC[C/T]CACAAAGAGAAGTAC | 388795 |
rs796517574 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32861564 | AAAGTGCTAGAAGTA[C/T]AGATGTGAGCCACCG | 388795 |
rs796663897 | snp | A/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32890560 | ACCTTCTGGATGCTC[A/G]ATGACTATTGAATGG | 388795 |
rs796704056 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32960030 | CAGGGACCCCCAACT[C/T]GCAGCCTTCATTCTT | 388795 |
rs796742049 | in-del | -/AT | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32880899 | AACTGTGGGCAAAAC[-/AT]ATATATATATAAAAC | 388795 |
rs796749370 | snp | C/G | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32872621 | CAACATGGTGAAACC[C/G]TGTCCCTACTAAAAA | 388795 |
rs796770131 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32950475 | TTATTTTAAATAAAC[C/T]TGAGAGGGGCGGCTG | 388795 |
rs796908508 | snp | A/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32864979 | CTCTCTGTTTTGCAG[A/T]TGAGGAAACCTGTGG | 388795 |
rs796949990 | snp | C/T | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32921201 | GATTATTTCTCTCTC[C/T]TTTTTTTTTCTTGAG | 388795 |
rs796972566 | in-del | -/TG | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32959228 | ATGGCTGCAATTTTA[-/TG]TGATAAGTAATGAGA | 388795 |
rs797011811 | in-del | -/AATC | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32933980 | GACTCCGTCTCAAAA[-/AATC]AATCAATCAATCAAA | 388795 |
rs797015095 | in-del | -/A | | | intron-variant | EFCAB8 | GRCh38.p7 | 20:32948999 | GGCAATTACAGAAGG[-/A]AAAAAAAAAGGCATT | 388795 |