| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs116576876 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692409 | TAAGAAGAACCTCAG[C/T]GAGTGCATTGAGTGA | 27342 |
| rs116577928 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748776 | ATCAATTGTATTTTT[G/T]TGCTAAATCACTTGG | 27342 |
| rs116637594 | snp | G/T | 0.030665 | 0.119967 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708751 | CAGGAGGTTGAGGTT[G/T]CAGTGAGGTATGATT | 27342 |
| rs116638963 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697321 | GGCTTGCAGCGTGGC[A/G]TCTCACAAGTCTTGC | 27342 |
| rs116732330 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780933 | TGTATTTTTATATTT[A/G]AAGTTAATTTCTTAC | 27342 |
| rs116733059 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712112 | TTACAACCAGCTTGC[A/G]TATGTCTACAAAAAT | 27342 |
| rs116820619 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718002 | TTTTGTATCTTCTAT[A/T]TTCCTGCTGAGGGTT | 27342 |
| rs116863549 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759075 | ATGCACATTTCATCT[A/C]ATACGTAGATTCCTG | 27342 |
| rs116906349 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796444 | TGGGAGTTGCAAATG[C/T]CTTTGTAATGTAGGA | 27342 |
| rs116913953 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806983 | CATACACTTGCCTAC[A/G]AGGGAAGAGCGTTTT | 27342 |
| rs116934109 | snp | A/G | 0.0256215 | 0.110247 | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760909 | GCTGGGATTGTAGGC[A/G]TGAACCATTGCACCT | 27342 |
| rs116938418 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719153 | GGGACAGTAGGGAAC[A/G]GCAATTAACACCAAA | 27342 |
| rs116940959 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805711 | AAGGCAAATTATGTA[C/T]AAGTTAATAAGGCTG | 27342 |
| rs116987395 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693745 | GAGGACTACGACCCT[C/T]AGGGAATCATTCATT | 27342 |
| rs116993744 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792185 | GAGGTAAAGGATTTA[A/C]TCACTGCTCTACTAT | 27342 |
| rs117010314 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779690 | AAAAAAAAAAAAACA[C/G]CAAAAACACAAGGTG | 27342 |
| rs117013788 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747541 | CTAAAATTAAAAATC[A/G]CTTTTGGGGGATTTT | 27342 |
| rs117015032 | snp | C/G | 0.219648 | 0.248151 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681479 | AGGGATCTCTGCACC[C/G]TCAACTTCCTGGGCT | 27342 |
| rs117020682 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761620 | CTGACACCAGCATTC[C/G]TCCCTCAGAGTACAG | 27342 |
| rs117032279 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803347 | CCTTTGGTATACCCC[A/G]CCGCCTGGCCAGAGT | 27342 |
| rs117040222 | snp | C/G | 0.0596104 | 0.162024 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722884 | TTTAGGGATTATTGG[C/G]ATTTTAACAATATTA | 27342 |
| rs117096093 | snp | A/C | 0.0123217 | 0.0776927 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740591 | CGCTCGACCCTTTGG[A/C]TCCACTCGCACTTCC | 27342 |
| rs117106945 | snp | C/T | 0.219349 | 0.248114 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726612 | GCTCAAGTAATCCCC[C/T]GACCTCAGCCTCCCA | 27342 |
| rs117139105 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719618 | AAACTTTTAGAAAAC[A/G]TAGAAGACAATACTT | 27342 |
| rs117148331 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736109 | GATGGAAAAAAACAA[A/G]ACAAAAAACAAAGCC | 27342 |
| rs117166130 | snp | A/G | 0.0599851 | 0.162463 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740601 | TTTGGATCCACTCGC[A/G]CTTCCTCCCGTCCAG | 27342 |
| rs117206083 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770484 | TATTATTTCAATTTT[C/T]TTCTCTTCTCTTCTC | 27342 |
| rs117221182 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697655 | CTCACCATTCACTGA[A/G]GATTAGCAGGGCGGG | 27342 |
| rs117268066 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805781 | ACAGGGTCTCACTCT[A/G]TCACCCAGGCTGGAG | 27342 |
| rs117271318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759299 | AAAGGTTAGTTGTGC[A/G]TTGAGCAGATTCTAC | 27342 |
| rs117296219 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683178 | AGATGGGATCTCACA[A/G]TGTTACCCAGGCAGG | 27342 |
| rs117306405 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799681 | GAATAAATTTTTTTT[A/C/T]TTTTTTTTGTACTTC | 27342 |
| rs117328880 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727709 | TCGCAGGGGTCCTGG[C/T]GGTGGCCAGAAGTGG | 27342 |
| rs117333571 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777644 | GAAACATTTCTGGAG[C/T]TGGGTGCAGTGGCTT | 27342 |
| rs117377066 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66685988 | CATCAGTGAAGTTAC[C/T]GCATTATAGGCCAGG | 27342 |
| rs117386388 | snp | C/T | 0.427879 | 0.175668 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730557 | ACTTGGTTTCTTTTT[C/T]TTTTTTTTTTTTTTT | 27342 |
| rs117396915 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793024 | TAGAAAAGGAGTTTT[C/T]GGCATTGTATTGTAA | 27342 |
| rs117468537 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776263 | AGGTCTCCCCTGAAG[A/G]CCGGGGAATGAATAA | 27342 |
| rs117474484 | snp | A/T | 0.0777841 | 0.181223 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803917 | AAGAAAGAAAGAAAT[A/T]TTTCCCTGGGAGAAG | 27342 |
| rs117489724 | snp | A/G | 0.145642 | 0.227177 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761838 | GGCAGGTCACTTGAC[A/G]TCAGGAGTTCGAGAG | 27342 |
| rs117490516 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761982 | CTTGAACCCGGGAGG[C/T]AGCGAAGGTTGCAGT | 27342 |
| rs117501560 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790875 | TTCTAGAGTTCATGA[A/G]TCACGCTGTATCTGC | 27342 |
| rs117517487 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764948 | TTCTGGGCCCTTGTT[A/C]TCTTCTGCATTTTAG | 27342 |
| rs117553313 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721515 | TCATTAAATGCAACA[A/G]TGCAGCATCATCAAA | 27342 |
| rs117554683 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729605 | CCACCTTTACCTTCA[C/G]CTTCACACCTGTCCT | 27342 |
| rs117583512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716339 | GTGCAGCGGCTCATG[C/T]GTGTAATCCCAGCAC | 27342 |
| rs117608556 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710997 | AAAAAAAATAATAAA[A/G]GAAATAAAAAAACTT | 27342 |
| rs117625221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724898 | GATTCAGGTTCATTG[A/G]TCTTGTCTTTGTAGT | 27342 |
| rs117634543 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732749 | TCTTGCTGTCTCTCT[C/T]GCTCTCTTGCTGTCT | 27342 |
| rs117637847 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761778 | AGCCTGGGGGTGGGC[A/G]TGGTGTCTCATGCCT | 27342 |
| rs117647643 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782602 | TAACCCCCACAAATA[A/G]CTGGCACTATAGGTA | 27342 |
| rs117681343 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716048 | TGAAGAGTCCAACTA[C/T]AATTTTGAGTTTGTC | 27342 |
| rs117682426 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696976 | ATACATGGGAGTCTC[C/T]ATGGTGCAGCCAATG | 27342 |
| rs117698657 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808790 | TGTTTACTTTAGCTT[C/G]TGTTTTAAATGGTCT | 27342 |
| rs117699827 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683184 | GATCTCACAATGTTA[C/T]CCAGGCAGGTGTCAA | 27342 |
| rs117719951 | snp | G/T | 0.0599851 | 0.162463 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744915 | AAAATGTTATCAGCC[G/T]CACACGGTGGCTCAC | 27342 |
| rs117737004 | snp | A/T | 0.231482 | 0.249313 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772925 | TCAAAAAAAAATAAA[A/T]AAATAAATAAATAAA | 27342 |
| rs117778448 | snp | C/T | 0.0520825 | 0.152737 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811341 | CATCAATACAACGGC[C/T]GGAGTTTCTGTTTTT | 27342 |
| rs117778830 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743197 | CCGTAATGCTAGCTA[C/T]TCAGGAGGCTGAGGT | 27342 |
| rs117870539 | snp | A/G | 0.166832 | 0.235761 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683701 | GGGGAACCAAAGGAG[A/G]GGAGGCCAGTAACTA | 27342 |
| rs117881067 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758961 | TACAGACAGGTCCTG[C/T]GTACTCTTCTAGTTT | 27342 |
| rs117888257 | snp | A/G | 0.0998734 | 0.199905 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752787 | AAGTGATATTGATGT[A/G]CATTCAAGTCTGAGA | 27342 |
| rs117901987 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720868 | AATTGAATTTCCATA[A/T]GCTAGCTCAAACAAT | 27342 |
| rs117911730 | snp | A/G | 0.0607341 | 0.163335 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754947 | GGGTGGCAAACCATG[A/G]GAGGATTGCTTGAGG | 27342 |
| rs117920224 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725511 | CATGTTGTGGCATGT[A/G]TCAGTTCTTGTTTCT | 27342 |
| rs117929604 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738413 | TGTCTTTAGCACCAA[C/T]CTCTTCTGCTCAGCC | 27342 |
| rs117981871 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712659 | GTATCGTTGGTAGAG[A/G]CAGGGTTTCACCATG | 27342 |
| rs118006240 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696756 | GGCTGGGAAACACTG[A/G]CAGGCATGGGAGAGC | 27342 |
| rs118011757 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746096 | AATGATCTGGACTAT[C/T]GTTACAATATGTAAA | 27342 |
| rs118020877 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730644 | GCTCACTGCAATGTC[C/T]GCCTCCCAGTTCAAG | 27342 |
| rs118021998 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728489 | ATAACCATGACCTTC[A/G]ATTTCATGACCCACA | 27342 |
| rs118073157 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786107 | CTGAGATCCAGGAGA[A/G]TGATCTGCTCTTGCC | 27342 |
| rs137881522 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744283 | CACGCCTGTAATCCT[C/T]GCACTTTGGGAGGCC | 27342 |
| rs137892865 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777843 | AATTTTGTTTTAAAA[A/T]TATGTATGCAGAATG | 27342 |
| rs137921826 | snp | C/G | 1.66513e-05 | 0.00288537 | intron-variant, missense | RABGEF1 | GRCh38.p7 | 7:66783734 | ACCAGCATTGAAACG[C/G]ATAGAGTGTCTAAGG | 27342 |
| rs137987481 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710652 | ATATAAAGCATTTGT[C/T]CATATACCATACCTG | 27342 |
| rs138007978 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773604 | GCCTGGTGATGCTGC[A/G]CTGCTGTCTGGGGAA | 27342 |
| rs138020304 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696100 | TGAGTCAGGGTCTCA[C/T]TGTTGCCCAGGTTGG | 27342 |
| rs138052792 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66740996 | CGTTCCAGGCCGCCC[G/T]CGGCTCCCTTAATCC | 27342 |
| rs138073312 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731905 | ATTCAAGGTTCATCC[A/G]ACGCCCCTGAGATGT | 27342 |
| rs138085797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811512 | TATTATTAATATTCT[C/T]ATGCTACAGAGGTTT | 27342 |
| rs138130511 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800560 | CTGCTAGGCTATGGC[A/G]TAGGTCATGACTACT | 27342 |
| rs138188489 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691943 | GCATCTGTAGTCCCA[C/G]CTACTGTGGAGGCTG | 27342 |
| rs138195238 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767518 | TATAGTATGTAAACT[G/T]TTAAGATGGCTGCTA | 27342 |
| rs138259335 | snp | C/G | 0.0633504 | 0.166319 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704677 | TTAGCCGGGCGTGGT[C/G]GTGGGCGCCTGTAGT | 27342 |
| rs138280421 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782622 | CACTATAGGTATGCA[A/C]TACCATGCCTGGCTA | 27342 |
| rs138291462 | in-del | -/GT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702357 | TTGTTTGTGTGTGTG[-/GT]TGTGTGTGTGTGTGT | 27342 |
| rs138331062 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716445 | TCTCTACCAAAAATG[C/T]AAAAAATTAGCTAGG | 27342 |
| rs138355023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795473 | GTGCTTCTGCACTTT[A/G]TTCAGCTACAAGCAG | 27342 |
| rs138373606 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735593 | GAGGTGACAGGATCA[C/T]TGTGGGGGGGGTTTC | 27342 |
| rs138399637 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751175 | AGCTGGAATTACAGA[C/T]GTGCGCCACCGCACC | 27342 |
| rs138499358 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746224 | TACTTTTATGGTGCT[A/G]TTTTGAAGTTTCCTG | 27342 |
| rs138499684 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795216 | TTTCTTCCTTTTCAC[C/G]TAATAAAACCCTGTC | 27342 |
| rs138505509 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804568 | GGTGAAACCCCGTTT[C/T]TACTAAAAATACAAA | 27342 |
| rs138519093 | snp | C/G | 0.0596104 | 0.162024 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686274 | CAACAAAGTGAGACT[C/G]TGTCTCAAAAAAAAA | 27342 |
| rs138629137 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696427 | GGGCGTGGTGGCTCA[C/T]GCCTGTAATCCTAGC | 27342 |
| rs138640399 | in-del | -/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785873 | AGCGAGACTCCATCT[-/G]GGGGGGAAAAAAAAA | 27342 |
| rs138725838 | snp | A/T | 0.000203149 | 0.0100764 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773746 | TTTCAACTTACTGCA[A/T]CCTCTGCTTCCTGGG | 27342 |
| rs138730967 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703471 | ATGATGTCAGGTAAA[A/G]ATACATGAGGTGGGG | 27342 |
| rs138744161 | in-del | -/GA | 0.0134861 | 0.0810011 | intron-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758586 | GGTCTGTCTGCCCAG[-/GA]GAGAGAAGGAGTTGA | 27342 |
| rs138771241 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781922 | CTCTGTTTGTTTCCC[A/T]TCTTTGAGGAGTTAA | 27342 |
| rs138774527 | snp | A/G | 0 | 0 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727562 | CCAGCTTGGGTGGAG[A/G]GATGAGATGTTTGGT | 27342 |
| rs138779271 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727982 | TCATCCTCCCCTCTC[C/T]TGACAGCTCTCCACA | 27342 |
| rs138809530 | in-del | -/AA | 0.226188 | 0.248863 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796238 | AGTTTAAAAAAAAAA[-/AA]GAGCTTCAAGTTTTT | 27342 |
| rs138815918 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686884 | TATAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG | 27342 |
| rs138841319 | snp | C/T | 1.73345e-05 | 0.00294397 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66772072 | AGGACTGGGAGCTGG[C/T]GGAGCGGTAAAAGGA | 27342 |
| rs138943560 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712270 | AGATTCCTTTTAAAA[A/G]CATTTTGACATTTCT | 27342 |
| rs138945189 | snp | C/G | 0.0154538 | 0.0865337 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681460 | CCGGGCTGGAGTTCA[C/G]TGGAGGGATCTCTGC | 27342 |
| rs138983223 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785936 | AAAACCTTTAAATTA[A/G]TGTTATTACCACCAA | 27342 |
| rs138990171 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752033 | CCCCATCTATATAAA[C/G]AAACCAAAAAAAACC | 27342 |
| rs139013947 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766245 | GCTCGGGAAGTCAAG[C/G]CTGCAGTGAGCTGTG | 27342 |
| rs139037345 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708311 | TTTCTTTTGAGACAG[G/T]GTCTCACTCCAATTT | 27342 |
| rs139068375 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693511 | GCCAAGTGTCTGGTC[A/C]CCTGACTACTCCTCC | 27342 |
| rs139072354 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771381 | CCTGATTTTGTTATC[C/T]GCCCTCCTCAGCCTC | 27342 |
| rs139080855 | snp | A/T | 0.0637235 | 0.166737 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728620 | CCCAACTTCATTTTC[A/T]CCTCCATCCTCATCA | 27342 |
| rs139094037 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757322 | AGATTTCATGTACCT[A/G]TCTAGCTTATTTCAC | 27342 |
| rs139114861 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806978 | TGAAACATACACTTG[C/G]CTACGAGGGAAGAGC | 27342 |
| rs139224714 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718961 | CCACATACTTCTTAC[C/G]ACTGCATCTTTCTTC | 27342 |
| rs139232628 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801899 | CTGGAGACTTATTTA[G/T]TTAGTTAGTTAGTTA | 27342 |
| rs139244488 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708532 | GACCTCAAGTGATCC[A/G]TCCACCTCTACCTCC | 27342 |
| rs139252730 | snp | A/C | 0.0596104 | 0.162024 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724451 | TGCACCCACCGCTTC[A/C]CAGGTTCAAGCAATT | 27342 |
| rs139263517 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737573 | TAGTTTAAAACAATT[A/T]AAAAAAAGATGAAAG | 27342 |
| rs139314444 | snp | C/T | 0.144632 | 0.226711 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721115 | GTAGGGATGGGGTTT[C/T]ACCAGGTTGGCCAGG | 27342 |
| rs139329582 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752632 | TGTGGTGTTTTCTTT[A/G]TAGCAGTGGTTCTCA | 27342 |
| rs139379757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687857 | CTGGGAGGCTGAGGC[A/G]GGCAGATCCCTTGAG | 27342 |
| rs139406196 | in-del | -/AAAC | 0.333407 | 0.235676 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692063 | CCCTGTTTTCTTAAA[-/AAAC]AAACAAACAAACAAA | 27342 |
| rs139509491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736848 | CCAGGGCGACAGAGC[A/G]AGACTCCATCTCAAA | 27342 |
| rs139509579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807234 | CCTCTTCTTGCCTGA[C/T]TCAGAGTCTGTCTCC | 27342 |
| rs139537496 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688191 | GAGACAAGGGAATTC[C/T]ATACTGATGAAAAGT | 27342 |
| rs139625763 | in-del | -/ATT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764325 | AATTGTTAATTTTTA[-/ATT]TTGAGTTGTAAGAAT | 27342 |
| rs139641011 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784185 | ACCATTGTTAGGCCA[C/G]TGGCAGTAATTTTAA | 27342 |
| rs139650506 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788783 | ACATAGTGAAATCCC[A/G]TCTCTACTAAAAATA | 27342 |
| rs139660553 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683653 | TTGAAGAATGAGTAA[C/G]ATTCAGACTAACAGG | 27342 |
| rs139702192 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779457 | TGCAGTGAGCCAAGA[A/T]CGTGCCATTGCACTC | 27342 |
| rs139734787 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742768 | CGTGCCACCACACCC[A/G]GCTGATTTTTAAATA | 27342 |
| rs139758018 | snp | A/C | 0.0599851 | 0.162463 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793123 | CGGGTCTCTAAAAGG[A/C]GCTCAGAGAGTTTCT | 27342 |
| rs139819470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770369 | TGGTTTCAGTTTGAA[C/T]GGAAATTGTTGCATA | 27342 |
| rs139822161 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713289 | TGGGACTACAGGTGC[C/T]CGCCACCATGCCCAG | 27342 |
| rs139828183 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791511 | ATATGGACATGAAAG[C/G]TAATACCTAAATAGA | 27342 |
| rs139880524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763071 | GGTGCAGTCATAGCT[C/T]GCTGCAGCCTCAAAT | 27342 |
| rs139942660 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733054 | CCAGCTCCTTAGCCG[C/T]GTAGTCAAGGTTCCT | 27342 |
| rs139946164 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723330 | TTTGCCATTTTGTCA[C/T]CTTTGACCCATTAGC | 27342 |
| rs139947928 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717944 | TTAATTTTAAAACTC[A/T]GTAATTGTATATTAT | 27342 |
| rs140016128 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701583 | GTGTAGTCTCAGCTC[A/T]CTGTAACCTCCACCT | 27342 |
| rs140017012 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747202 | AATGTGGTTAAAAGT[A/C/G]AGAAGTTAGAATAAG | 27342 |
| rs140029644 | snp | A/T | 8.24083e-05 | 0.00641852 | missense | RABGEF1 | GRCh38.p7 | 7:66809137 | CATAGATTGGACAGA[A/T]GGAATTGCAAGAGAA | 27342 |
| rs140097123 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732976 | GTGGCAAGTCCAACC[A/G]TATGACTGTGTCCCT | 27342 |
| rs140102363 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743189 | GGCGCCTGCCGTAAT[A/G]CTAGCTACTCAGGAG | 27342 |
| rs140148550 | in-del | -/T | 0.157642 | 0.232314 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691376 | TGTACACAGCCCAGA[-/T]GTCTGTACCCAGAAG | 27342 |
| rs140220507 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729715 | GTCTCCTGCCATCAC[A/T]AAATACTTCTTAATA | 27342 |
| rs140257325 | in-del | -/T | 0.0865458 | 0.189163 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772454 | GCATTATTTCCCTCA[-/T]TTCTTTTAATATATA | 27342 |
| rs140311303 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706656 | CCTGACCTCATGATC[C/T]GCCCGCCTCGGCCTC | 27342 |
| rs140321326 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784623 | TAGAAAAGCAGCAGG[G/T]TGTTTAACTGTTTAG | 27342 |
| rs140368593 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701141 | AAGAAGGACTGGAGG[A/G]GTAGACAGGCACTGC | 27342 |
| rs140392476 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776986 | CCACACTGAGGGACA[A/G]TAATACCTACCAGAG | 27342 |
| rs140498015 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810452 | GCCATATCACCCCTC[C/T]GTTAAGAACCACTGA | 27342 |
| rs140573300 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702052 | CCCATTAAGCTGTCA[C/T]TCCCCAATCTCCCAT | 27342 |
| rs140601808 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803061 | TTAGAATAAGTTCCA[C/T]ATAAGTAGAAAAAGA | 27342 |
| rs140606493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780129 | AGCAATAAAGGAAAT[A/G]AGTAGGATTTTCCTG | 27342 |
| rs140626639 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689317 | GCTAGATTTACTAAG[-/A]AAAAAAAAAGAAAAC | 27342 |
| rs140667427 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794495 | TTTATCTTTTAAATA[C/G]CCTTTAAATATTCTT | 27342 |
| rs140675140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716266 | GCATTTACGTAACAT[A/G]TCTTTTTCCATTTTT | 27342 |
| rs140701613 | in-del | -/AAAAC | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788456 | CTCAAAAAAAAACAA[-/AAAAC]AAAACAAAACAAAAC | 27342 |
| rs140712228 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781539 | CACCCAATAGGCCAC[A/G]GTGTGTGATGTTCCC | 27342 |
| rs140795747 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793864 | TTCCACAGGATGTAT[C/T]GGCCCTTGGCGTGTG | 27342 |
| rs140832726 | in-del | -/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698102 | CATCACAGCCACGCA[-/C]CCCCCCCCACCCTCA | 27342 |
| rs140841519 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744003 | AAATGTTTTCAGTGT[A/G]GTGCTTGATTATTTG | 27342 |
| rs140937254 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774784 | CAAAAAAAGGATCCT[A/G]TTTATCCTTTAAGAC | 27342 |
| rs140987753 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773269 | TGCCTGATGCTGTCA[A/G]TAGCAGATCCTGTTT | 27342 |
| rs141008420 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726997 | TGTCGCAGCAAGACT[C/G]CATCTCAAAAAATAA | 27342 |
| rs141010933 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776340 | GTGACTTTTGCTGTT[G/T]CCTTTTGTTTTATTA | 27342 |
| rs141024718 | snp | C/T | 0.00594254 | 0.0541845 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799279 | CAAGACAAATGGCCA[C/T]AGTTTATCCTTGGAG | 27342 |
| rs141037025 | in-del | -/TT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687114 | GCCACCACGCCCGGC[-/TT]TTTTTTTTTTTTTTT | 27342 |
| rs141051484 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681076 | TGACAGAGCGCGACT[A/G]TCTCAAAAAAGAAAA | 27342 |
| rs141052084 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771698 | ATATGGCTGTGTCAG[G/T]AATTTACTATATTTA | 27342 |
| rs141086463 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785610 | CCGGGTGCGGTGGCT[A/C]ACGCCTGTAATCCCA | 27342 |
| rs141114237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720976 | AAGCTTGAGTGCAGT[A/G]GCACAATCTTAGCTC | 27342 |
| rs141125871 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790072 | GATACTGAGGACTTG[C/T]AGCAGATCAGCCAAA | 27342 |
| rs141129432 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740488 | GACTAGGAAACGCCG[A/G]TTTCTCCGGGGCTCC | 27342 |
| rs141198009 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703752 | TCCAACTTTGTTCTT[G/T]TTCAAGACTGTTTTT | 27342 |
| rs141202411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732518 | TATCTCCCACTGGGT[A/G]TCCCCAGTCACTCAC | 27342 |
| rs141275886 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695920 | GCAGTGAGCTGAGAT[C/T]GCACCACCGTACTTC | 27342 |
| rs141321419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698431 | AGAGTGCAAGGTCCC[C/T]ACCCACCATGGGCTC | 27342 |
| rs141323037 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, missense | RABGEF1 | GRCh38.p7 | 7:66783681 | TCCCAGCAGAAATTC[A/G]GGAAGCAAAAGCTCC | 27342 |
| rs141328856 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806778 | CCTCCCAAGTAGCTG[A/G]GATTACAGATGTGTG | 27342 |
| rs141378456 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687454 | TCCAGACTCCATAAC[C/G]AAGAGAAGTAAATTT | 27342 |
| rs141381318 | in-del | -/CT | 0.0596104 | 0.162024 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700884 | CTGGCCCTGTCCAGA[-/CT]CTCATACTGTGGGGC | 27342 |
| rs141398152 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795320 | TGAACTAAGGAAAAG[G/T]CCGGCAACAATGGAT | 27342 |
| rs141419612 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752246 | CGCCTGTAATCTCAG[C/T]GCTTTGGGAGTCCGA | 27342 |
| rs141499132 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770844 | GATATCTCATTGTGA[C/T]TTTGATTTGCATTTC | 27342 |
| rs141524259 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745471 | TAGCCCATCAGTAAA[C/G]TTATCACACCATAGG | 27342 |
| rs141568177 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772769 | TTAAAAAAGTTAGCC[A/G]GGCATGGTGGTACGC | 27342 |
| rs141568184 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721139 | GGCCAGGCTGCTCTC[A/G]AACTCCCGAGCTCAA | 27342 |
| rs141649584 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804617 | GCGGGCATCTGTAAT[C/T]TCAGCTACTTTAAAG | 27342 |
| rs141682149 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766751 | TATTTTCGAGACAGG[A/G]TTTCACTCTGTTGCG | 27342 |
| rs141720924 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800574 | CGTAGGTCATGACTA[C/G]TCTGCCCCCCGCACC | 27342 |
| rs141745026 | in-del | -/GA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737094 | AGAGAGAGCGAGAGC[-/GA]GAGAGAGAGAGAGAG | 27342 |
| rs141767363 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692093 | CAAATAAATAAATAA[A/G]TAAAAGTGTATAAAT | 27342 |
| rs141782289 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734760 | TCCTGTGGGAGACCA[A/T]TGGGTGCATGATATT | 27342 |
| rs141815835 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725283 | GAGAATTGTACATCC[A/G]TCATCATAATCAATT | 27342 |
| rs141821372 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756268 | CAGATTGACAAAAAA[G/T]TAAAGTTCGATAATG | 27342 |
| rs141850345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728232 | CTATCCCATCTGCTG[C/T]CTGGGTTCTGCCTGG | 27342 |
| rs141891016 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731452 | CTGTGCATGATGGCT[A/C]ACACCTGTAATCTCA | 27342 |
| rs141893177 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720195 | TTATTATTATTATTA[A/T]TTTTTTTTTTTTTTC | 27342 |
| rs141948503 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785854 | ACTCCAGCCTGGATG[A/G]CAGAGCGAGACTCCA | 27342 |
| rs141957039 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708203 | GTTGTTACTTTTACT[A/G]TATATTTTTTAGTTC | 27342 |
| rs141983641 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749699 | CAAACAGGCCAGGCA[C/T]GGTGGCTCACACCTG | 27342 |
| rs141988607 | in-del | -/G | 0.078151 | 0.181571 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725965 | ATCCCACTTAGAAAA[-/G]CCCCCATTCATCAGG | 27342 |
| rs142098517 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744444 | GAGGCTGAGGCAGGC[A/G]GATCACGAGGTCAGG | 27342 |
| rs142186863 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747885 | TAATGACTTACAAAG[A/G]TACGTGCGACATACT | 27342 |
| rs142187624 | in-del | -/TA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720190 | TATTATTATTATTAT[-/TA]TTATTTTTTTTTTTT | 27342 |
| rs142226170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786100 | AAAATTTCTGAGATC[C/T]AGGAGAGTGATCTGC | 27342 |
| rs142233426 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707077 | GGCGTGAGCCACCGC[G/T]CCCGGCCCGTACTGG | 27342 |
| rs142280137 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712625 | ATAGGTGTGCACCAC[C/G]TCACCCAGCCAATTT | 27342 |
| rs142299762 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806979 | GAAACATACACTTGC[C/G]TACGAGGGAAGAGCG | 27342 |
| rs142315190 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709483 | TACAGTATTACAGTG[A/G]TACCATAGAAAATAT | 27342 |
| rs142328562 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737442 | CAATACGAGACTGGG[-/T]AGGGGGGGGCAGTCT | 27342 |
| rs142344404 | snp | C/T | 0.000280869 | 0.0118472 | missense | RABGEF1 | GRCh38.p7 | 7:66809205 | AGCCTCCGAATCAAC[C/T]GTTAGCAGCTATTGA | 27342 |
| rs142380853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802543 | CAGGCTGGGGAGGGA[A/G]ATTATTAGACAGCAG | 27342 |
| rs142389530 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725162 | CATATTTTCCCACTT[A/C]CTTACATGTCTGTAC | 27342 |
| rs142444469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737423 | CACACCTGGCTATCC[C/T]ACGCAATACGAGACT | 27342 |
| rs142491094 | in-del | -/AAC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719187 | CAACCAACCAACAAA[-/AAC]AACATCACAAAAAAC | 27342 |
| rs142523027 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773615 | CTGCGCTGCTGTCTG[G/T]GGAATCATACTTGGA | 27342 |
| rs142532178 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715427 | TGGGCCTCTGTGCCC[A/G]CCTCTTCTTTTCTAA | 27342 |
| rs142638327 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788666 | GTTTCATTGTTATTT[C/T]TCTAGCCAGTCCTAT | 27342 |
| rs142653534 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692551 | TCACCTCTCCAAAAG[C/T]GACAGGTAAAGGGAT | 27342 |
| rs142669768 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693980 | GTTTGGTTAATTTTT[C/T]GTATTTTTAGTAGAG | 27342 |
| rs142678717 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735633 | GCTGTTCTCGTGATG[A/G]TGAGTGAGTTATTGT | 27342 |
| rs142689955 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696125 | GGTTGGAGTGCAGTG[A/G]CACAATCATAGCTCA | 27342 |
| rs142734897 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786306 | GTTTTTTGTTTTTAG[A/C]ATTTAAATTTCAGCA | 27342 |
| rs142739356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782128 | TCATACCGATGTCAA[C/T]ACAATCTTTGGTTTT | 27342 |
| rs142775654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791119 | ACCTTTATGAAGAAC[A/G]TATGCGTTCCTTAGA | 27342 |
| rs142831425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795758 | AGCAGTGCCTTTGAA[C/T]TGTACCATGCGTATC | 27342 |
| rs142905341 | in-del | -/C | 0.0314385 | 0.121371 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793735 | CAGTCAAGGTGATCA[-/C]AAAGTGCCATGAGTG | 27342 |
| rs142966747 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779408 | GCTTGGGAGGCTGAG[G/T]CAGGAGAACTGTTTG | 27342 |
| rs142972830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701384 | GCGCACACCAGTAGC[C/T]CCAGCTACTAGGGAG | 27342 |
| rs142986910 | snp | G/T | 4.94531e-05 | 0.00497234 | missense | RABGEF1 | GRCh38.p7 | 7:66809099 | AGGATCATGAATGAA[G/T]CCAAGAAACTGGAAA | 27342 |
| rs143058249 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746410 | CTGGGTTCAAGGATT[C/G]TTCTGCCTCAGCCTC | 27342 |
| rs143109343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714152 | GGTGTTTTTTCTGTT[C/T]TAAATCTTTGGTAAG | 27342 |
| rs143109430 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761930 | GTGGCAGGCACCTAT[A/G]GTACCAGTTACTTGG | 27342 |
| rs143126913 | snp | A/G | 1.65157e-05 | 0.0028736 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66775311 | CTCCAAGTTTGAAGA[A/G]AAGAAAACCAACGAG | 27342 |
| rs143128210 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806007 | ACCTTGACCTCCCTA[A/G]GAGTTGGAACTGCAG | 27342 |
| rs143132006 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719583 | AAATAATTAAGGAGG[G/T]AGTAATATGAATCCC | 27342 |
| rs143148045 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717654 | GCCTTGACCTCCCCA[A/G]GCTCAGGAGATCTTC | 27342 |
| rs143174037 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723472 | CATACTTTCATTTCA[A/G]TCTTCCATTTTTTAT | 27342 |
| rs143193400 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739640 | GAACTCCAGTGTGGG[C/T]GACAGAGTGAGAGTC | 27342 |
| rs143212084 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730342 | ATCGACAGGGGATAA[A/C]CAATAGGCTCCACCA | 27342 |
| rs143223578 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778775 | AGAAGCCAGCTTGGA[A/G]GGGTTTCCACTGGCC | 27342 |
| rs143250207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763568 | TCTCCCTTTTGAAGT[A/G]CACACTTAAGTGACA | 27342 |
| rs143254867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795304 | GGATCCCGTCTTTAG[C/T]TGAACTAAGGAAAAG | 27342 |
| rs143296626 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776005 | AAGAGGATTGTCACT[G/T]AAGTCACAGTTGTTC | 27342 |
| rs143346284 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66685312 | GCACTCGCCACCATG[C/T]CCAGCTAATTACTTC | 27342 |
| rs143348639 | in-del | -/ATTTTTTTTTTTTTTTTTTACA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804085 | GATTCCAGTAGCTGG[-/ATTTTTTTTTTTTTTTTTTACA]ATTTTTTTTTTTTTT | 27342 |
| rs143357656 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790341 | CATGAGGTCTTTTTT[C/T]CGTCTTTCTTCACAT | 27342 |
| rs143374711 | snp | C/T | 0.000153988 | 0.00877328 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66795566 | TCTACCACAATGTGG[C/T]CGAAAGGATGCAAAC | 27342 |
| rs143429361 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780462 | ACTTAGTGCATAATA[A/G]GCATTATCTATATGT | 27342 |
| rs143517799 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741635 | TTTACCGGAGCACCT[A/T]GGGAGTTGGTTTTTG | 27342 |
| rs143523675 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696755 | GGGCTGGGAAACACT[A/G]GCAGGCATGGGAGAG | 27342 |
| rs143550884 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701976 | GTGGCATTAAGTACA[A/T]CCACAATATTGTGCA | 27342 |
| rs143596123 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703012 | GTCTCGCTCTGTCGC[C/T]GCCCAGGCTGGAGGG | 27342 |
| rs143611516 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781193 | TCTTTGTTCTGTTTT[C/G]TTTTTGTTACTGGTT | 27342 |
| rs143631435 | snp | A/T | 0.00770626 | 0.0615934 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783643 | TGGATCTTTTATGTC[A/T]TGAAACTTACTATGT | 27342 |
| rs143642606 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757547 | TATATAAATATTTGA[A/G]TGAATGCAGAGGGAA | 27342 |
| rs143650632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800208 | GGCTCCTTTTGTTAC[A/G]GGAACCAGAGACTCA | 27342 |
| rs143669687 | snp | C/T | 0.0146672 | 0.084371 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66755910 | GTCCAAGCTAACGTT[C/T]GGACAAATAATGTTT | 27342 |
| rs143789623 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750212 | TTGTCTAGGGTTTTA[A/G]AAGTTGTATAGTCAT | 27342 |
| rs143847636 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760196 | CCTCTTCCTTGCCTT[C/T]GACACTCTTAACCTG | 27342 |
| rs143851711 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732300 | CATTGAGCAGGGGGT[G/T]CGAGGCCTCTGGGGC | 27342 |
| rs143858295 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686558 | GCACTGTAGAAACGT[A/G]TGTTATTTCACATGG | 27342 |
| rs143901817 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800421 | TTCTGCTTCTCTTTA[G/T]CTTCCCGTGTCAACT | 27342 |
| rs143912119 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721310 | TGTCTTACTGCTACT[C/T]TAACATATGCCATAT | 27342 |
| rs143927772 | in-del | -/TG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702380 | TGTGTGTGTGTGTGT[-/TG]GTGTGTGTGTCAGCT | 27342 |
| rs143955356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759212 | GTTTCGTAATTCGTT[C/T]GAGGCTCTCACAGGA | 27342 |
| rs143967594 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684652 | TTGTTTGTTTGTTTT[G/T]GATACTGAGTCTCAC | 27342 |
| rs144000395 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736911 | ATCTAATTATACACA[C/T]ATGCACAGACACCTA | 27342 |
| rs144041622 | in-del | -/TTAT | 0.496633 | 0.0408914 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683728 | ACTACAAGGAGGTGC[-/TTAT]TTATTTATTTATTTA | 27342 |
| rs144049250 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801961 | CACCCAGGCTGGAGT[A/G]CAAGTGGCAACGATC | 27342 |
| rs144106825 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796069 | TTGAACCCGGAAGGC[A/G]GAGGTTGCAGTGAGC | 27342 |
| rs144188770 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737598 | TGAAAGACTGATATA[A/G]TGCTGTTCTCCTTTA | 27342 |
| rs144208218 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743019 | TGTGTGGTTAAAATG[A/G]GTCTCTCTGGCCAGG | 27342 |
| rs144288182 | snp | A/C/G | 0.00716713 | 0.0594884 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786440 | GCAGTGTGTTGCTCT[A/C/G]TCTCCTGGACTGGAG | 27342 |
| rs144375845 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714896 | GCCAAGATCCTGCCA[C/T]TGCACTCCAGCCTGG | 27342 |
| rs144390975 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783006 | TGTCCCATTTTCCTT[G/T]CAGTGTGTTTATTTG | 27342 |
| rs144438108 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774142 | TTTCATTCTTGATTT[A/C]TCTTTTATCTCCCAT | 27342 |
| rs144452728 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798576 | GCTGCAGGGTAGTTG[A/G]AGTGCAGTTAGGGTG | 27342 |
| rs144461361 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758985 | CTAGTTTGCCTAATG[G/T]TTACATGTTACATAA | 27342 |
| rs144531912 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789255 | ATAGGCTTTAATTAT[G/T]GTGAGAACTTCAGCA | 27342 |
| rs144657470 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716019 | GCTGATTTTCTATCT[A/G]TTCTGTCCATTCTTG | 27342 |
| rs144702649 | in-del | -/TTG | 0.0134861 | 0.0810011 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770969 | TCGGATTATTTGGGT[-/TTG]TTGTTGTTGTTGTTG | 27342 |
| rs144713113 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792777 | ACATTTATTCATTCA[A/G]CCCATACTGAGCACT | 27342 |
| rs144732668 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776461 | GCTTTGGGAGGCCAA[A/G]ACAGATGGATTACCT | 27342 |
| rs144734019 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747328 | GAAGCAGGAATGTAA[A/C]AAGAGTTTTGAGGGC | 27342 |
| rs144763654 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701251 | GGCCTGTAATCTCCA[C/T]GCTTTCAGAGGCTGA | 27342 |
| rs144768966 | snp | A/G | | | utr-variant-3-prime | RABGEF1 | GRCh38.p7 | 7:66809392 | CTTATAAATGTCAGC[A/G]TTTTTTAAAGGTACA | 27342 |
| rs144779294 | snp | A/G | 0.00164601 | 0.0286408 | missense | RABGEF1 | GRCh38.p7 | 7:66805218 | GCAAGCACATCTTCA[A/G]TGCCATCAAGATCAC | 27342 |
| rs144792815 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697127 | GTGAGGGTGGAGGGG[A/G]TGCAGAGCAGGAGTG | 27342 |
| rs144796977 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774916 | TAGCAGCTGTCCCAT[G/T]CTGTAGCAGTTGTTT | 27342 |
| rs144908253 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694025 | TGTTGGCCAGGCTGG[C/T]CTCGAACTCCTGGCC | 27342 |
| rs144912427 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772175 | CTTCTGCTTTGAGCT[A/G]TCAGCAAGTCAGTTT | 27342 |
| rs144968633 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790233 | GAAGAACCTCTGTGA[A/C]ACTCTCAACAATGAG | 27342 |
| rs145086373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754758 | ACGTCTAGGCATTGC[A/G]TTTTGTATTTCTCTA | 27342 |
| rs145098048 | in-del | -/CTGAGAC | 0.0228947 | 0.104514 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768648 | CATATATGTGCTGAT[-/CTGAGAC]CTGCATAGTGGTCTC | 27342 |
| rs145102260 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785079 | ATGTTTTAGAAAATT[A/G]CTCAACTCAGATTTG | 27342 |
| rs145133438 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712143 | CCTGCTCAGATTTTG[A/T]TCTGTGTTTTGTTAA | 27342 |
| rs145185521 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698187 | TTAGACCATCATTTC[A/G]GAGCAAGACTATGTC | 27342 |
| rs145232217 | in-del | -/TA | 0.0715223 | 0.175059 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739977 | CTTCTGGATGTCGGT[-/TA]TGTTTTTTTTGAGAC | 27342 |
| rs145248247 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709411 | CCCATTACAGTGTAC[A/C]TAAGCATCACTATAA | 27342 |
| rs145322674 | snp | C/T | 0.0182019 | 0.0936463 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680861 | CCAAGGCGGGCGGAT[C/T]ACTTGAGGTCACGAT | 27342 |
| rs145349505 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771556 | CGGGAAGCTTTTCCC[C/T]TAAGTTTTTTTTCTA | 27342 |
| rs145372196 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724865 | TTGCTTTTTTCCCTT[A/G]GTGCTTTAGTTTAGA | 27342 |
| rs145496572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695952 | GCGTGGGTAACAAAG[C/T]GAGACTGTCTCAAAA | 27342 |
| rs145524137 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733001 | GTCCCTTTAGCCTGA[C/T]GCCCTTCCCCAGCTC | 27342 |
| rs145526060 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688887 | CACCTGAGGTCAGGA[C/G]TTCAAGACCAGTCTA | 27342 |
| rs145563422 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811267 | GTATCTCATATTGGT[C/T]GAATTCTTCTGGTAT | 27342 |
| rs145579105 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731825 | ACACTTTATGTCATA[C/G]TGGAGAAACTGAGGC | 27342 |
| rs145597413 | in-del | -/A | 0.0107246 | 0.0724382 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759091 | TACGTAGATTCCTGT[-/A]AGCCACCACCATAGT | 27342 |
| rs145645266 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730063 | GCTGTGCCATAGACT[A/C]AGGGTGGCCTCCAAA | 27342 |
| rs145648384 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714997 | AAAACTTTCGTCGTC[C/G]TCCTCCTCCTCCTCT | 27342 |
| rs145706561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733293 | GGGGGAGTTGACCAC[C/T]CCCTCGAGGCTGCCC | 27342 |
| rs145716216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703378 | CCAAATCCCAGGTCT[C/T]GGAGATTTACCTCTG | 27342 |
| rs145726460 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781745 | CCCTCCGTAGTGTTT[C/G]CATGATATTTTGCCA | 27342 |
| rs145745788 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716433 | GACGAAAACCTGTCT[C/G]TACCAAAAATGCAAA | 27342 |
| rs145756364 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795055 | AGCCAGCCTGCCCAC[C/T]GGGGTGGAGTTTTGG | 27342 |
| rs145788066 | in-del | -/GGGG | | | | | GRCh38.p7 | 7:66779842 | GAATCCCTATTGGCT[-/GGGG]GTTCAAACATAAGTC | 27342 |
| rs145801763 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808134 | ACCTCAGAGAGCTTA[A/T]GTAACTTTCCCACGG | 27342 |
| rs145811538 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707285 | TTTCATGTGTACTTC[A/C]GAAGAATGTGTATCA | 27342 |
| rs145828639 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688683 | GAAGATGAAATCATA[C/T]AGGAAATTAGAAAAC | 27342 |
| rs145902875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712931 | GTCATCCTCCCACCT[C/T]AGCCTCCCAAATAGC | 27342 |
| rs145908846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790929 | ATTTTAAATGAACAA[A/G]ATGTCTTTGGGAATT | 27342 |
| rs145938973 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762780 | GCATTGGGTCCAATA[C/T]GGAGATGAGGGTTGG | 27342 |
| rs145949268 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769381 | CTTCTAGCTGTCACC[C/T]GTGTGTCTGCACACC | 27342 |
| rs145953582 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693165 | AAGGGGGAGATTCGG[A/G]GACAGGGTATTTGGA | 27342 |
| rs145971603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807174 | TAGCAGCTTCTAGTG[C/T]CCTTGGCCTGCAGCC | 27342 |
| rs145986239 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727961 | CCTCAGGCGTCTCCA[C/T]CAACCTCATCCTCCC | 27342 |
| rs146057875 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743169 | TAAAATTAGCTTGGT[A/G]TGATGGCGCCTGCCG | 27342 |
| rs146068723 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746781 | GGCTCCTGCCACCAC[A/G]TCCGGCTAATTTTTT | 27342 |
| rs146077581 | in-del | -/A | 0.0197687 | 0.0974348 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716660 | GTCATGTCTTTTTTT[-/A]AAAAAAAACTCTTCT | 27342 |
| rs146109540 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708310 | TTTTCTTTTGAGACA[C/G]GGTCTCACTCCAATT | 27342 |
| rs146157668 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705280 | GGCAGTGCATGCCTG[C/T]CCCAAAAATGAACAT | 27342 |
| rs146179010 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724110 | TTCGTTTGAGAGAGG[C/T]TATTTTAATTGAATA | 27342 |
| rs146182414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801827 | ACTTCTGTGTGGCTA[C/T]GGGGGCAGTGGTTCT | 27342 |
| rs146197088 | in-del | -/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773096 | TTGTTTTTTTTTTTT[-/C]ATCCAGTCAGCCAAT | 27342 |
| rs146228619 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692226 | ATCACAGAAAGTTCA[A/G]CTGGGCAGTGCTGTT | 27342 |
| rs146229898 | in-del | -/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767000 | TTGCCTGTCAAGTTT[-/C]TTTTTTTTTTTTTTT | 27342 |
| rs146276879 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687669 | GGGAAATGTAAAAAA[A/G]TTAGTTAAATAAAAT | 27342 |
| rs146288300 | snp | C/T | 1.79716e-05 | 0.00299757 | utr-variant-3-prime | RABGEF1 | GRCh38.p7 | 7:66809306 | TTTAGTGGAGAGTAT[C/T]TATTTGAGCCTAAAT | 27342 |
| rs146297971 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761676 | TAAGACCAATCCAGA[A/G]TAGAGTCCTGCCTTG | 27342 |
| rs146310649 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708369 | CTTGGCTCACTGCAA[A/C]CTTCGCTTCCTGGGT | 27342 |
| rs146350696 | in-del | -/GA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737052 | ATATATATGAGGGGG[-/GA]GAGAGAGAGAGAGAG | 27342 |
| rs146444854 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802056 | CTGAGACCACAGGCA[C/T]GTGCCACCACACCCA | 27342 |
| rs146455905 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759492 | ACATAGTATATTAGT[C/T]CGTTCATTCTCACGT | 27342 |
| rs146462017 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765626 | TCTCTGCTTCTTGGG[A/G]TATGTCTATTTCATT | 27342 |
| rs146496339 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699050 | CACTGAGACAGAGCC[A/G]CATGGAGGAGCGGGG | 27342 |
| rs146510941 | in-del | -/GTTGA | 0.167809 | 0.236103 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773116 | AGTCAGCCAATATTT[-/GTTGA]GTGACTCCTTTGCTG | 27342 |
| rs146567776 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733766 | CCAGCACTTTGGGAG[C/G]CTGAGACGGGCAGAT | 27342 |
| rs146600540 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798635 | ATGGTGGTCCTGCCC[A/G]TGGCCTCCTATACAA | 27342 |
| rs146615884 | snp | A/G | 0.0271762 | 0.113356 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680910 | ACATGGTGAAACCCC[A/G]TCTCGACTAAAAATA | 27342 |
| rs146626029 | snp | C/T | 4.94515e-05 | 0.00497225 | missense | RABGEF1 | GRCh38.p7 | 7:66809100 | GGATCATGAATGAAG[C/T]CAAGAAACTGGAAAA | 27342 |
| rs146663528 | snp | A/T | 0.00557542 | 0.0525036 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680269 | TTTTTTTTTTGAGAC[A/T]GAGTTTCGCTCTTGT | 27342 |
| rs146679696 | in-del | -/AT | 0.0603597 | 0.1629 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762084 | AACAAAAACAAAAAC[-/AT]AAAATCCTAGGATGA | 27342 |
| rs146695507 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719889 | CACATATTTACTGAC[C/T]TTACAGAACAAGGTT | 27342 |
| rs146698558 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797986 | GCCAGGCATGGTGGC[A/G]CACGCCTGTGATCCC | 27342 |
| rs146720173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780557 | CAGAGTCAGATAGGT[C/T]AAGTTGGTTGATAGC | 27342 |
| rs146807338 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776120 | AAATTTATGTTGGTA[C/G]TCAGAGTTATGCAGT | 27342 |
| rs146819005 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779815 | CTTCTTCACTTCTTT[C/G]ATCTTACACACGGAA | 27342 |
| rs146919701 | snp | A/C | 0.0126979 | 0.078662 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740593 | CTCGACCCTTTGGAT[A/C]CACTCGCACTTCCTC | 27342 |
| rs146942822 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744221 | GCTAATTACTGCTAT[C/T]TTGTATTTTAATTTT | 27342 |
| rs147024154 | snp | C/G | 0.219049 | 0.248077 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721167 | CAAGTGATCTGCCGG[C/G]CTCGGCCTCCCAAAG | 27342 |
| rs147038500 | snp | A/C | | | utr-variant-3-prime | RABGEF1 | GRCh38.p7 | 7:66809391 | GCTTATAAATGTCAG[A/C]ATTTTTTAAAGGTAC | 27342 |
| rs147043305 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803900 | TCTCAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 27342 |
| rs147048364 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725909 | AATCAGAGGGGGAAG[A/C]TGTGACCCTTTCTTG | 27342 |
| rs147167945 | snp | C/T | 3.30278e-05 | 0.0040636 | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66797450 | CTATAAATATGTATT[C/T]TGTCCAGAAACTACT | 27342 |
| rs147171371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699603 | AGGCTGAGGCAGAAG[A/G]ATCACTTGAACCTGG | 27342 |
| rs147172353 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778078 | AAATTTTGCATTTCA[C/G]ACTGATTACTTTTGT | 27342 |
| rs147190947 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758393 | TCCCAGCAGCAGAGA[G/T]CATTTTTACTCTGTC | 27342 |
| rs147200522 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714451 | ATTTATGTCTCGTTT[C/G]CTTTCTTTTCTCTCT | 27342 |
| rs147268322 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703629 | TATTGGCTTTTTTTT[-/T]CTGGAACTCTATTTC | 27342 |
| rs147276785 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682944 | CGCTTTGGAGGCTAG[C/G]TCATAGGCAGCTGGC | 27342 |
| rs147278921 | snp | C/G | 0.0275645 | 0.114116 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756425 | ATTCCGTTTCTGTTT[C/G]TAGCAAACTGCTCAC | 27342 |
| rs147338072 | in-del | -/C | 0.0596104 | 0.162024 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751993 | TGAGCCCAGGACTTC[-/C]AAGACCAGCCTGGGC | 27342 |
| rs147384000 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736840 | CACTCCAGCCAGGGC[A/G]ACAGAGCGAGACTCC | 27342 |
| rs147403852 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795860 | AAAACATCTTAGGGC[C/T]TGGCTCAGTAGCTCA | 27342 |
| rs147413605 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800428 | TCTCTTTATCTTCCC[A/G]TGTCAACTCCTGTTG | 27342 |
| rs147414412 | in-del | -/TTAT/TTATTTAT/TTATTTATTTAT | 0.502942 | 0.246744 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766710 | TCCCACTGTTACCTC[-/TTAT/TTATTTAT/TTATTTATTTAT]TTATTTATTTATTTA | 27342 |
| rs147460726 | in-del | -/TTA | 0.0777841 | 0.181223 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764322 | AAAAATTGTTAATTT[-/TTA]TTATTGAGTTGTAAG | 27342 |
| rs147509165 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779086 | TGCCACTCCAGCCTG[A/G]GCAACAAAGTGAGAC | 27342 |
| rs147519091 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782189 | TGTTGCATTTTTTGT[C/T]TTAAATTAGATTGTA | 27342 |
| rs147519253 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732662 | TCCATCATGAAATTT[C/G]GTTCACAATTTTCCT | 27342 |
| rs147613065 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709433 | TCACTATAACTAGTG[C/T]TATCTACATAAAATA | 27342 |
| rs147663040 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804208 | TCTGCCTCAGCCTTT[C/T]CAGTAGTTGGGGCTA | 27342 |
| rs147814665 | in-del | -/TTTTC | 0.35574 | 0.226537 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744022 | CTTGATTATTTGCTT[-/TTTTC]TTTTCTTTTCTTTTC | 27342 |
| rs147822619 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748015 | GTCTTAAGTGCAGAG[A/G]GCCACAAATTTGGCT | 27342 |
| rs147842836 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789999 | GATACTCATGGAAGA[A/G]GTCAAGTTAGAAGAG | 27342 |
| rs147852671 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793109 | TAAGACAGGCCTCTC[A/G]GGTCTCTAAAAGGAG | 27342 |
| rs147927778 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729638 | CCTCCATTCTCACTT[C/G/T]CACTGTCTTCACTAA | 27342 |
| rs147947726 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772672 | CTAGCACTTTGGGAG[G/T]GTGAGGCAGGAGGAT | 27342 |
| rs147958080 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725249 | AACATGTACACTTTA[A/G]TGACCTTTAGTATAT | 27342 |
| rs147998612 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707577 | CCTGTAATCCCAGCT[A/C]CTCGGGAGGCTGAGG | 27342 |
| rs148029802 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722136 | CACTTCATCCTGGGC[A/T]ACAGAATAGGACCCT | 27342 |
| rs148052282 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698356 | GCCTGTCTCCCCATC[-/A]GGGGTGACAAGAGAG | 27342 |
| rs148053209 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781487 | ACCTACGTTAGGTAT[G/T]TCTCCTAATTAGGTT | 27342 |
| rs148063314 | snp | C/T | 0.167484 | 0.23599 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734512 | TGTTGGCCAGGCTGG[C/T]CTTGAATGCCTGACC | 27342 |
| rs148072715 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767995 | TGTATGGGTGCACCA[C/T]AGTTTGTTTATTCAT | 27342 |
| rs148082316 | snp | A/G | 0.00677665 | 0.0578135 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756005 | ATCATATGAAAGTTG[A/G]TGAACCTTGGATTAC | 27342 |
| rs148113871 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695897 | CTTACATCTGGGAGT[C/T]GGAGGTTGCAGTGAG | 27342 |
| rs148158773 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712972 | GGTGTGCCACTACAC[A/T]TGGCTAATTTTATTT | 27342 |
| rs148213617 | snp | A/G | 0.171704 | 0.237423 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745376 | TAGCAGAGATGACCT[A/G]TCCCTCAAATGTAGG | 27342 |
| rs148242527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762217 | AGGAAAATAAGGTCT[C/T]TGTCCTCAGCAAATT | 27342 |
| rs148275614 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699127 | GAGGCGAATTCCAGG[C/T]CCCTCTGGGTTTCCT | 27342 |
| rs148281810 | snp | A/G | 6.60229e-05 | 0.00574518 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66775324 | GAAAAGAAAACCAAC[A/G]AGAAGACCCGCAAGG | 27342 |
| rs148293873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717372 | ATCTATAAACATTGA[A/G]ATTCCATTAGAATCT | 27342 |
| rs148298681 | snp | G/T | 0.170733 | 0.237101 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690133 | TTGAGACGGAGTCTC[G/T]CTGTGTCGCCCAGGC | 27342 |
| rs148302516 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795318 | GCTGAACTAAGGAAA[A/T]GTCCGGCAACAATGG | 27342 |
| rs148347454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790355 | TTCGTCTTTCTTCAC[A/G]TGCGACAGGCAATGT | 27342 |
| rs148407181 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758990 | TTGCCTAATGGTTAC[A/G]TGTTACATAACTATA | 27342 |
| rs148442216 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774179 | TACAACTTGACCAAG[C/T]TCTATTTCTTCCAAC | 27342 |
| rs148469494 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715252 | CCTGCTTTAGTCTCC[C/T]GAGTAGCTGGGACTA | 27342 |
| rs148545913 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706321 | TATACTTTCATTTCT[C/G]TTATGCGATACCTAG | 27342 |
| rs148593263 | snp | A/T | 1.64917e-05 | 0.00287151 | missense | RABGEF1 | GRCh38.p7 | 7:66809052 | TGTATAAGAACTTGG[A/T]TCTCTTGTCTCAGTT | 27342 |
| rs148594471 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808145 | CTTAAGTAACTTTCC[C/T]ACGGTCACTCACTGT | 27342 |
| rs148595826 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701252 | GCCTGTAATCTCCAC[A/G]CTTTCAGAGGCTGAG | 27342 |
| rs148605963 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693290 | TTTCCACCCCCCAGG[A/G]CACCATCAAAAGTAA | 27342 |
| rs148617557 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796424 | TCATCAGCATTCATC[A/T]GTCTTGGGAGTTGCA | 27342 |
| rs148730514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709201 | TTTAGTAGAAATGGA[A/G]TTTCACCATGTTGTT | 27342 |
| rs148770620 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802307 | TTCCCTACAACAAAG[A/G]ATTATTCAACCCCAA | 27342 |
| rs148785712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783174 | CACCAACGAAATGGT[A/G]GGTAAATAATTGTGA | 27342 |
| rs148848235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750044 | TAACTGGTGTCTCAC[A/G]AGATAATACGTTTGG | 27342 |
| rs148910810 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702459 | TTCATCTACAAGTTT[G/T]TGTGTGAACTCATGT | 27342 |
| rs148912731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780636 | GTCAATTACTAAATG[A/G]GGAATATTGAAATCT | 27342 |
| rs148932358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695470 | AGGTTCCACAGTGGC[C/T]TGGCCCACATGTCAG | 27342 |
| rs148985104 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688713 | CACTTTGAGATGAAT[A/G]AAAATGAAAACACAA | 27342 |
| rs148986095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763798 | GGTTCACCATGTTGT[A/G]GCATATATCAGCACT | 27342 |
| rs149046557 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66685014 | AAGTGATTCTCTAGC[C/T]TTGGACTCCCAAAGT | 27342 |
| rs149056618 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710812 | CTTTAAAGATTTTCT[C/T]TCTTGGGGCTGAGCA | 27342 |
| rs149057974 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790324 | AGTTCCACCCTTATG[C/T]GCATGAGGTCTTTTT | 27342 |
| rs149097595 | snp | A/T | 8.3053e-05 | 0.00644357 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66775275 | CAGTCAGAGCAGCCA[A/T]GGGGCCCAATCCCTC | 27342 |
| rs149139855 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761389 | AATTAATTTGCTGAG[G/T]TGGTTTACAGAACTC | 27342 |
| rs149143934 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730200 | GCTCCTGTCCCCTGA[A/G]GGAGGACTTCCCAGC | 27342 |
| rs149234866 | in-del | -/AAAT | 0.0981418 | 0.198593 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692079 | AACAAACAAACAAAC[-/AAAT]AAATAAATAAATAAA | 27342 |
| rs149245985 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696535 | TCTCTACTAAAAATA[C/T]AAAAATTAGCCAGGC | 27342 |
| rs149299913 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767519 | ATAGTATGTAAACTT[A/T]TAAGATGGCTGCTAT | 27342 |
| rs149342759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747272 | AGTATTAAGCTTTTT[A/G]ATTTTCCCCCAGTAA | 27342 |
| rs149372525 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792194 | GATTTACTCACTGCT[C/T]TACTATCTTTTTTTC | 27342 |
| rs149404034 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701147 | GACTGGAGGGGTAGA[C/T]AGGCACTGCCATCCA | 27342 |
| rs149415747 | snp | C/T | 0.000461163 | 0.0151779 | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66805210 | CAAGTGCAGCAAGCA[C/T]ATCTTCAATGCCATC | 27342 |
| rs149419616 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681806 | CTCCACCTCCCATTC[A/G]CGCTTCCACCGTGGC | 27342 |
| rs149429418 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755333 | CAAAAAATTTAGCCA[A/G]GGATGGTGATGCACA | 27342 |
| rs149448536 | snp | C/G | 0.0648419 | 0.167978 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778052 | GATCACTTAATATAA[C/G]TTAGCCAGGTAAATT | 27342 |
| rs149458705 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732146 | CAGGCCACCGCCCTC[C/T]CTTCCTATGGTCCAG | 27342 |
| rs149510525 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727936 | CCAACAAGACCCCCA[A/G]ACACCCTTGCCTCAG | 27342 |
| rs149512688 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805937 | TTTTTGAGAGATGGG[A/G]TCTCGCTGTGTTGCC | 27342 |
| rs149606538 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782930 | CAAAGACCAAGTGGT[A/G]GTTCATACTTTCTGA | 27342 |
| rs149649251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704912 | TTGCAGCTGGCCTAT[A/G]TTTAGTTTTTTAAGA | 27342 |
| rs149677764 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801557 | ATTACCCTTCCCAGC[C/G]TCTGGTAACCATCCT | 27342 |
| rs149691664 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688576 | AAGTATTTTATAATC[A/G]TCATGGAATGAAACT | 27342 |
| rs149697057 | snp | A/G/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794039 | AATTTGTTTGCTTTC[A/G/T]TCTTTTGAACCCTGA | 27342 |
| rs149706545 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744092 | ACTGGGCTGGAGTGC[A/T]GTGGCATGATCTTGG | 27342 |
| rs149718901 | in-del | -/TTGT | 0.0777841 | 0.181223 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757281 | CTTTCTAACTTGTTA[-/TTGT]TTCTCTGTTACAAGA | 27342 |
| rs149745361 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683914 | CCCAGCTGATTTTTA[A/C]AGATTTTGTAAAGAT | 27342 |
| rs149758818 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779768 | ATTATGAACTGTAAC[A/G]TGGATGAGGTTGTTC | 27342 |
| rs149782006 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733099 | TAAGGCATTGGTGCT[A/C]TCTGGTTCCCTCTCC | 27342 |
| rs149837579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807854 | GATGGTTTCTACCCC[A/G]ACTGTTTCCCAGGCT | 27342 |
| rs149899803 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724504 | AGCTGAGATTACAGG[C/T]GCATGCCACTGCGCC | 27342 |
| rs149973876 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708577 | TACAGGCGTGAGCCA[C/T]CGCCCCTGGCCAGCC | 27342 |
| rs149985322 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697926 | CCTGATCCTATTTCC[C/T]TCCATGAGCCTCTTC | 27342 |
| rs150046799 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771473 | TGATATAATGTATTT[G/T]TCTGATTTTGCTTTT | 27342 |
| rs150049846 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741978 | CGTCTCTACTACAAA[A/T]AAAAAAAAAAAAGAA | 27342 |
| rs150100556 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735290 | ATTCCAACCGTGTGT[A/G]TCCCTGATCTCACTC | 27342 |
| rs150148487 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810732 | AGGCCCCAGGGCACC[A/G]TTCTAGAACAACGTC | 27342 |
| rs150223104 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727343 | GGGTTCTCTGGACTC[A/T]GGGCCTAGGGCTTCC | 27342 |
| rs150276230 | snp | A/G | 1.82131e-05 | 0.00301765 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799281 | AGACAAATGGCCACA[A/G]TTTATCCTTGGAGCT | 27342 |
| rs150289789 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710312 | TAGGTTGTTTTTTAG[C/T]GTTTAGCTTTTACCA | 27342 |
| rs150305156 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777189 | TTTAGCTTAAGGTCT[A/G]TTTCTTGATGATATG | 27342 |
| rs150357152 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773395 | TGTCCCAGAGAAAGA[A/G]GGGTCCCGATTCCAC | 27342 |
| rs150425764 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691692 | ACATTTTATTACAAA[A/G]TAGGGTTTGTGTTCA | 27342 |
| rs150433755 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767391 | TTTTATTAGATTTAT[G/T]TAAACACCTCCACAA | 27342 |
| rs150486701 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760922 | GCGTGAACCATTGCA[C/T]CTGGCCCTGGGGAAG | 27342 |
| rs150584765 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696192 | CGCTTCTGGCCCCCA[A/G]GTAGCTGGGATTACA | 27342 |
| rs150589857 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800616 | GAACCCCATAAGAGG[C/T]TGAAGGTGGAGGCCT | 27342 |
| rs150613109 | snp | A/C/G | 0.00438476 | 0.0466401 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791159 | GCTGCTAAAAATGAC[A/C/G]GATTTCTGGCTTTTT | 27342 |
| rs150673669 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741823 | AGGCGTGAGCCATTG[C/T]GCGGCTTTAACTGCT | 27342 |
| rs150769094 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718140 | CTGAGGCCAGGAGTT[C/T]GAGACCAGCCTGGCC | 27342 |
| rs150789795 | snp | A/G | 0.00108059 | 0.0232191 | intron-variant, missense | RABGEF1 | GRCh38.p7 | 7:66783725 | AACCGGCAAACCAGC[A/G]TTGAAACGGATAGAG | 27342 |
| rs150822051 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752474 | ACTCCAGCCTGGGGA[A/G]CAAGAGTGAAACTCC | 27342 |
| rs150834487 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737498 | ATCCGGATTTCGGGG[C/T]TCAGCCTTGCCATGG | 27342 |
| rs150851279 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795368 | TGGATAGGTTTTACT[C/T]TCCTGCAGGATTAAT | 27342 |
| rs150867731 | snp | C/G | 0.148326 | 0.228391 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745663 | GATCTCAGCTACTCG[C/G]GAGTCTGAGGCACAA | 27342 |
| rs150925210 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793355 | ACATTTTAAGCAGTT[C/T]TGTGCATGTAACAGT | 27342 |
| rs151073590 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773028 | TAGAATTCTAAAACT[C/G]CTTCAACAGAAGAAA | 27342 |
| rs151089666 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720539 | CAGCAAACTAAATAT[A/G]AAAGGGAACTATCTC | 27342 |
| rs151152582 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709667 | GTAATCCCACCTACT[C/T]AGGAGCCTGAGGCAG | 27342 |
| rs151204153 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706600 | ATTTTTAGTAGAGAC[A/G]GGATTTCACCATGTT | 27342 |
| rs151240046 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737073 | GAGAGAGAGAGAGAG[A/T]GAGAGAGAGAGAGCG | 27342 |
| rs151265144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743984 | CTATGTAGCTGATAA[A/G]GATAAATGTTTTCAG | 27342 |
| rs151276303 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730378 | TCTACCACATAAAGG[A/C]ATCTTAAACGGTAGG | 27342 |
| rs151285636 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810064 | TTTCCCTCATTCATT[C/T]AGCAAATCTCTATTG | 27342 |
| rs151294045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760808 | TTGAACATTTTTAAA[C/T]AATAGAGACAGAGTC | 27342 |
| rs151297832 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66685324 | ATGCCCAGCTAATTA[C/G]TTCTGTCTTGTATTT | 27342 |
| rs151336531 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802726 | TGAAGCATGTGGAAG[A/C]GATCCCTGGGGGTGT | 27342 |
| rs180683316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799804 | ATAGAGGAAGGGAAC[C/T]GGTAAGGCAAGGTAA | 27342 |
| rs180683961 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66809855 | GTTTGTCCCACTAAA[A/G]TGACTCGAGAAGTGT | 27342 |
| rs180693653 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767069 | GTGCAATGGCATGAT[C/G]TTGGCTCACTGCAAC | 27342 |
| rs180694905 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785059 | TAGCATGTATGCTGT[A/G]TAATATGTTTTAGAA | 27342 |
| rs180701909 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792567 | TAGGGATCCTTATTA[C/G]ACAGTAAGCAGTCTA | 27342 |
| rs180703950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752293 | CAAGGTCAGGAGTTC[A/G]AGCCCAGCCTGGCCA | 27342 |
| rs180706802 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774632 | AGGTGTGGTGGTGTG[C/T]GCCTGTAGTCCCAAT | 27342 |
| rs180711303 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758867 | TTTTTATTAAAAAAC[A/G]TTCATGTGTGATTTT | 27342 |
| rs180715695 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744590 | GGAGAATGGCGTGAA[C/G]CTGGGAGGTGGAACT | 27342 |
| rs180721335 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728344 | TCAGGGACCCTGACT[G/T]GTTGGGGGAGGCTGC | 27342 |
| rs180815501 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694486 | CACAGAGGGCCCGGC[A/G]GGGCCTGGAGGGCAG | 27342 |
| rs180823866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686499 | TTTCATAGTACAGGC[C/T]GAACATTTTGAAAAT | 27342 |
| rs180831486 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707021 | CGATCTCCTGGCCTC[A/G]TGATCCACCCGCCTC | 27342 |
| rs180916980 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788968 | TGTCTCAAAAAAAAA[A/T]AATAATAATAATCTG | 27342 |
| rs180927069 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795109 | GGAGGAGCCTGGCCC[C/T]TCTTCTTTCTGTGTG | 27342 |
| rs180929697 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772735 | CCAACATGGTGAAAC[A/C]CCCTCTCTACTAAAA | 27342 |
| rs180931576 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755821 | GAGAATGCTCCCCTG[C/T]TTGCTCTGCTCATTC | 27342 |
| rs180932020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805086 | ATGATTTTCCTATTG[C/T]TTCTTTTTTGTGATT | 27342 |
| rs180941879 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742556 | AACAGGGTGGAGTGA[C/G]GGAGAGGGGGGAATC | 27342 |
| rs180948344 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724886 | TTAGTTTAGATAGAT[G/T]CAGGTTCATTGATCT | 27342 |
| rs180968139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778041 | TTTGTTTCACAGATC[A/G]CTTAATATAACTTAG | 27342 |
| rs180993330 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747437 | ATTGTACAAAGACCT[A/C/T]ATGAACCACATTTGA | 27342 |
| rs181014351 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760927 | AACCATTGCACCTGG[A/C]CCTGGGGAAGGGATT | 27342 |
| rs181018879 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715006 | GTCGTCCTCCTCCTC[A/C]TCCTCTTCTTCTTCC | 27342 |
| rs181026648 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732728 | CACTCTCTCTCGCTC[A/T]CTCTCTCTTGCTGTC | 27342 |
| rs181057313 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690750 | ATTAAATTTACAAAA[A/G]GAGAAAACACTGCCA | 27342 |
| rs181062665 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709280 | GCTGGGATTATAGGT[A/G]TGAGCCATCGTGCTC | 27342 |
| rs181145066 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682686 | TGGGACGCTCGGACC[C/G]AGACCACAGCCCCCG | 27342 |
| rs181146194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792806 | CTAACCCTGTGCCTG[A/G]CCTTGTTCTAGGCAT | 27342 |
| rs181147939 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810462 | CCCTCCGTTAAGAAC[C/T]ACTGATGTCTTTTAC | 27342 |
| rs181149348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703001 | TTTGAGAAGGAGTCT[C/T]GCTCTGTCGCCGCCC | 27342 |
| rs181161033 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774852 | TCCCCCAGCAGATTG[A/C]GTTGTTCTTTCCTGT | 27342 |
| rs181242332 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758972 | CCTGTGTACTCTTCT[A/G]GTTTGCCTAATGGTT | 27342 |
| rs181250868 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783025 | TGTGTTTATTTGAAG[A/T]GGGGAAAGAATTGTC | 27342 |
| rs181259640 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728525 | ATTCCCATTTCACCA[C/T]TGCCATCACCAGTGT | 27342 |
| rs181278821 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736448 | GAAGAAGGGGAGTGG[G/T]AAGAGCATTTTGGGC | 27342 |
| rs181284733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718681 | TCGCAGTATTCAGAT[A/G]TGTCCTGAGTATGTA | 27342 |
| rs181306797 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798829 | TAGCTGGGCATGGAG[A/G]TGGGCGCCTGTAGTC | 27342 |
| rs181315451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744807 | GCTTTCTCAACCCCA[A/G]TTGAGCACACAAGTG | 27342 |
| rs181337700 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765959 | TTATAGTACAAAATT[A/T]AAAAAAACTTAATTG | 27342 |
| rs181380273 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696917 | TTGGTGATGGTGGAT[A/G]CAGGAAGGGGAAGAA | 27342 |
| rs181388872 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706570 | GTGTGCCACCACGCC[C/T]GGCTAATTTTTTGTA | 27342 |
| rs181460652 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803183 | CACAGTAGCCTCATA[A/C]GTAAGGGAATAAAAG | 27342 |
| rs181472590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747917 | TTGGTAACATAACAG[A/G]TAAGTGGGTGAGGAA | 27342 |
| rs181475530 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771379 | CTCCTGATTTTGTTA[C/T]CCGCCCTCCTCAGCC | 27342 |
| rs181478785 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787272 | CTCCTGACCTCAAGT[G/T]GTCTGCCCGCCTTGG | 27342 |
| rs181483614 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732809 | TCTCTCGCTTTTGCT[C/T]TCGCTCTCACTCTGT | 27342 |
| rs181489760 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795975 | GAAACCCCGCCTCTA[C/T]TAAAAATACAAAAAG | 27342 |
| rs181492304 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715481 | TCCCCTTTAATTTGG[A/C/T]GGCATCGTGTAAGTT | 27342 |
| rs181492666 | snp | A/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754006 | CAACGTACTAGGCCA[A/T]TTTTTTTTTTTTTTG | 27342 |
| rs181498445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763151 | TACAGGCGTGAGCCA[C/T]TGCCCCTAGTCCACA | 27342 |
| rs181507155 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686164 | TGTGTGCCTGTGATC[C/T]CAGCTACTCGGGAGT | 27342 |
| rs181524611 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741388 | GGCTGCGGGGCCGGG[G/T]TTAGGAGCAGAAGTC | 27342 |
| rs181578921 | snp | A/C/G | 0.00557542 | 0.0525036 | utr-variant-5-prime, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66682152 | GTGTGAGGCTGGAGC[A/C/G]GACTGGGGAACCCAG | 27342 |
| rs181587949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702026 | ACTCAAAAAGGGCAG[A/G]GCATCCAATACCCAT | 27342 |
| rs181628886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778500 | CATTCCAAAGTGCCC[C/T]TTTCTTTCAGAACTC | 27342 |
| rs181663220 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799077 | TCAGTCTTGGTAGCA[C/G]TGCGTAATGTCATTT | 27342 |
| rs181670479 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724371 | TATTTATTTTATTTT[A/T]TTTTTTTGAGACGGA | 27342 |
| rs181682537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766233 | AGTATTGCTTGAGCT[C/T]GGGAAGTCAAGGCTG | 27342 |
| rs181685684 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752264 | TTTGGGAGTCCGAGG[G/T]GGACGGATCACAACA | 27342 |
| rs181696692 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737049 | TATATATATATGAGG[G/T]GGGAGAGAGAGAGAG | 27342 |
| rs181720483 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692421 | CAGCGAGTGCATTGA[C/G]TGATATTGGTGTGAG | 27342 |
| rs181782626 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707300 | AGAAGAATGTGTATC[A/G]TATTGTTGTTGGGTA | 27342 |
| rs181854206 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719324 | TTACCATCTTAGCCT[C/T]CTGAGTAGTTGGGAA | 27342 |
| rs181859354 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744082 | TTGATCTGTGACTGG[A/G]CTGGAGTGCAGTGGC | 27342 |
| rs181874013 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796474 | ACAGGGAGTGACCTT[G/T]CTGAAGTCTCCCCAT | 27342 |
| rs181894323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714706 | TTTGGGAGGCCCAGG[C/T]GGGCGGATCATGAGG | 27342 |
| rs181929507 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711474 | TTGCCAAACAATATC[C/T]AATATTCCAGCACCA | 27342 |
| rs181975924 | snp | C/T | 0.0487999 | 0.148386 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692078 | AAACAAACAAACAAA[C/T]AAATAAATAAATAAA | 27342 |
| rs181983468 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709734 | GAACCAAGATCAAGC[C/T]ACTGCACTCCAGCCT | 27342 |
| rs182051487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788157 | GTAGTGCTTTTTAAT[A/G]AACTTGGGGCTGGGC | 27342 |
| rs182079504 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755436 | AGCTGTGATCATGCC[A/T]CTGCACTCTAGCCTG | 27342 |
| rs182100266 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759566 | GAGGTTTAATTGGCT[C/T]ACAGTTCTACAGGCT | 27342 |
| rs182103449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724433 | GGCGCGATCTCGGCT[C/T]ACTGCACCCACCGCT | 27342 |
| rs182107587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745661 | GTGATCTCAGCTACT[C/T]GGGAGTCTGAGGCAC | 27342 |
| rs182111150 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730115 | CCTCCCTTTCTCATC[C/T]CTAAGATGAAAAGAG | 27342 |
| rs182112324 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758689 | TCTGGGTGTGCCGAC[C/T]CTCCTGCCTTCTACC | 27342 |
| rs182119135 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713304 | CCGCCACCATGCCCA[A/G]CTAATTTTTTGTATT | 27342 |
| rs182126606 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727953 | CACCCTTGCCTCAGG[C/T]GTCTCCACCAACCTC | 27342 |
| rs182239056 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695773 | GAGTTTGAGACCAGC[C/G]TGGGCAACATGGTGA | 27342 |
| rs182320307 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806922 | GTGTTGGGATTACAG[G/T]CATGAGCCACCGCAC | 27342 |
| rs182324927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689009 | GGGGCAGGAGAATTC[C/T]TTGAACCTGGGAGAG | 27342 |
| rs182330867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708685 | GGCATGATGGCACAC[A/G]CCTGTGTTCCCAGCT | 27342 |
| rs182338255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791233 | GTTCCCATCACCTTT[A/G]TTTTGCCAGTAATTG | 27342 |
| rs182352148 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803580 | CCACTGCTTGGACTT[A/G]GTGATAGTTGTGGGT | 27342 |
| rs182370125 | snp | C/T | 0.00100859 | 0.0224339 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771847 | TATTTAGTAGAATGA[C/T]AATTCATTTTCAACA | 27342 |
| rs182388397 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738203 | TTTGTATTTTTAGTA[C/G]AGGTGGCGTTTCACC | 27342 |
| rs182389828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742449 | ACCGAGGAAGGAGCC[A/G]GGCATTTAGGCCATG | 27342 |
| rs182407700 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737085 | GAGTGAGAGAGAGAG[A/G]GCGAGAGCGAGAGAG | 27342 |
| rs182475220 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767551 | GTCTGAATCTTTGTC[G/T]GTCCCCCAAATTCAT | 27342 |
| rs182487336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752356 | AAAAATTAGCCAGGT[A/G]TGGTGGCGGGCACCT | 27342 |
| rs182492633 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738607 | TGTGCTGGCACACAC[C/T]TATCATCCCAGCTAC | 27342 |
| rs182500831 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721795 | CAACGTGGTAGAACC[C/T]CGTCTCTACTCAAAA | 27342 |
| rs182566115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692980 | CATGCCGGAAGGGGC[C/T]GGCACCTCCCTGCTG | 27342 |
| rs182572978 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712540 | CAGTGTCGTGATCAC[A/G]GCCCACTGCAGCCTC | 27342 |
| rs182583847 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697862 | GCTTCATGTCCAGGG[A/T]AAAAAGGTCCAGGAG | 27342 |
| rs182587956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793891 | TGTGAGGTCAGTGGC[C/T]TGTGTAGATGAAGTC | 27342 |
| rs182634323 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780890 | TGTTTCAGAGTATGC[C/T]TTTCCTTTCATTAGT | 27342 |
| rs182655988 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748854 | ACCAATCTGTTTGCA[A/C]GTCTGCACTGTTTCA | 27342 |
| rs182657538 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720435 | ACTCCTAGCCTCAAG[C/T]GATCCACTCACCTCA | 27342 |
| rs182670724 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716845 | GTGCAGTGGTGCAAT[C/G]TCGGTTCACCACAAG | 27342 |
| rs182675690 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680316 | CAATGTCGTGATCTC[A/G]GCTCACTGCAACCTG | 27342 |
| rs182684538 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699489 | TGAGGTCGGGAGTTC[A/G]AGACCAGCCTGGCCA | 27342 |
| rs182708797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764245 | GGAACATCTTTTCAT[A/G]TACTCACGACTGTTT | 27342 |
| rs182708813 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805560 | CAAGGACCAGGCCAT[A/G]CAGACACTCCGCCTC | 27342 |
| rs182713246 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750659 | CACATATAATGGTGC[C/T]TGAGAAATAAGTTGA | 27342 |
| rs182718616 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789815 | CATCCTGGGGCAGCC[A/G]TGGTGGCTCCATGCG | 27342 |
| rs182719841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773066 | GGAATTCTGCCAACT[C/T]CTCTAGCTAGTTGTT | 27342 |
| rs182721287 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734741 | CCTGGCCCCAAAGGA[A/G]CACTCCTGTGGGAGA | 27342 |
| rs182728716 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716975 | GTAGAGACGGGGTTT[C/T]GCCATGTTGGCCAGG | 27342 |
| rs182859290 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684328 | GCCTACCTGTAATCC[C/T]AGCTACTCAGGAGGC | 27342 |
| rs182896952 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683390 | CATTTTGCTTTTAAG[A/G]GTTACTGATTCATAT | 27342 |
| rs182898508 | snp | A/G | 0 | 0 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796912 | GTTTTTTTTTTAAGC[A/G]TATTTTTAAATATAA | 27342 |
| rs182904740 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703628 | GTATTGGCTTTTTTT[C/T]TCTGGAACTCTATTT | 27342 |
| rs182911665 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785130 | AGTGTGATGTGTTCT[A/T]ACTCTGTAATAATTT | 27342 |
| rs182917979 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800694 | TACTAGAAAGTTCAA[A/G]ATCAGCTGGTTTACA | 27342 |
| rs182920799 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763688 | ACTACTCTATTTTCT[A/G]TCTCTAGATTTCCCT | 27342 |
| rs182935181 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785746 | GGGCGTGGTGGCAGG[C/T]GCCTGTAGTCCCAGC | 27342 |
| rs182941653 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734539 | GACCTCAAGTGATCC[A/G]CCCATGTTGGCCTCC | 27342 |
| rs182943107 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768347 | ATCTTCTTTGTTAAA[A/G]TGTCTGTTGAGGTTT | 27342 |
| rs182948507 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752716 | CCCTTTCCCAGGCCA[G/T]TTGAATCAGAAACTC | 27342 |
| rs183122257 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729587 | TCACTTCCATCCTTA[C/T]TTCCACCTTTACCTT | 27342 |
| rs183126624 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687375 | AGGTGATCCATCCTC[C/G]TCGGCCTCCCAGAGT | 27342 |
| rs183141815 | snp | A/T | 0.00835141 | 0.0640778 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680255 | TTTGTTTTCTCATTT[A/T]TTTTTTTTGAGACAG | 27342 |
| rs183166338 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707768 | TTACTGCAGTTTTTA[C/G]TTCATGTACTTTGAG | 27342 |
| rs183174060 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703969 | CTTTAATCTCTTTCA[A/G]CAATGTTGTGTACTT | 27342 |
| rs183184568 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775971 | TTCACCCTGCTTTTT[A/T]AAATGCCATATAACC | 27342 |
| rs183204908 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745871 | AGGCCAAAGTGGGAG[A/T]ATCGCTTGAGCCTAG | 27342 |
| rs183211829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797576 | ACTGGGGGGAAAATA[A/G]TGCACCTGTGTTTCA | 27342 |
| rs183248759 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742897 | CAGGCATCAGCTACC[C/G]AGCCTGGAGGGTCGT | 27342 |
| rs183326771 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779436 | TTGAACCTGGGAGGT[A/G]GAGATTGCAGTGAGC | 27342 |
| rs183327230 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763515 | TCTGTTTTTTAAAAA[A/G]ACAGCTTTATTGAGG | 27342 |
| rs183333161 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726935 | CCTGAACCCAGGAAG[C/T]GGAGATTGCAGTGAG | 27342 |
| rs183339951 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748205 | CCTTATTGGCTTTTT[A/G]TGTAAGACGGTGACA | 27342 |
| rs183345788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733148 | TTCCAGGTGAGGTGA[C/T]TCCTGGAAAGTCTTG | 27342 |
| rs183399328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683060 | AGGAAATTTTCCCAG[A/G]ACGAGTTTACCGGAG | 27342 |
| rs183413582 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688069 | CAGCCTGGGCAACAA[A/G]AGTGAAACTCTGTGT | 27342 |
| rs183446077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781238 | AGAATACATCTTTAA[C/T]TTACCTACCTTCAAG | 27342 |
| rs183483541 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756225 | CCTTAGGGAAATGCA[C/T]GTTAAATGATTTTTT | 27342 |
| rs183491561 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810967 | CTGGTTCCCAAGCTC[A/G]CACAGAAGGTGATAA | 27342 |
| rs183495337 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725808 | CACAAGGAGCTCCCC[C/T]GAAAAGTAAGTCTGA | 27342 |
| rs183519906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774984 | GGGAAAAGGATTAGA[C/T]TTGATTTCTTTCATG | 27342 |
| rs183528718 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722217 | GGGGCTGTGGTGGGT[G/T]GGTCATGAGGTCAAG | 27342 |
| rs183533508 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745533 | ACACTTTGGGAGGCT[C/G]AGGTGGGCAGATCAC | 27342 |
| rs183568726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775628 | ATCAAGAGAATTGAA[A/G]TAGGTACTTTTGCTT | 27342 |
| rs183568932 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793530 | TAGTAATAATCACAA[G/T]AATGAATATAGTTTC | 27342 |
| rs183669632 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691005 | CTGGGGCATGAGAAT[C/T]GCCGGAACCGGGGAG | 27342 |
| rs183679797 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709377 | TCATAATGGAAATAA[G/T]AGTATTGTAATTTTC | 27342 |
| rs183737320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793075 | GCTGGGGGAGGAGAA[C/T]ATGATCCCTTGACAC | 27342 |
| rs183750571 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739122 | TGCCTGGCTAATTTT[A/G]TATTTTTAGTAGAGA | 27342 |
| rs183754804 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759489 | GTCACATAGTATATT[A/C]GTTCGTTCATTCTCA | 27342 |
| rs183786487 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790500 | ACATGCTGGTTTAGG[G/T]GAAAGAGCTGAGCCC | 27342 |
| rs183810793 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756504 | TTGGCTATCAAAGAT[A/T]TATAAATTGTGTTAG | 27342 |
| rs183845702 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773668 | GCTTGTGCTTTTTGT[G/T]TGTTTGTTTGTTTTT | 27342 |
| rs183848313 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757255 | CTATTATGACTGATA[C/T]CTTTTTTATACTTTC | 27342 |
| rs183855551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743563 | CTGGAGTGCAGTGGC[A/G]CGATCTCGGCTCACT | 27342 |
| rs183865097 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727155 | TCTTTTAATAAAAGC[A/G]ATACATTCAAAATTG | 27342 |
| rs183905198 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694400 | GATCAGTGAGGCACC[A/G]TTAGGAGTGATGAAC | 27342 |
| rs183942083 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698758 | TCTCAGTGTGGGTGG[G/T]TCTGACTCTGCCACC | 27342 |
| rs183978023 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806386 | ATTGTATAAGCTTCA[A/G]GTTCCTCCAAACTTG | 27342 |
| rs183982330 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773541 | CACAGAGTCTCTGAT[C/T]TTAGTGGCTTGGGAG | 27342 |
| rs184005276 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743205 | CTAGCTACTCAGGAG[G/T]CTGAGGTAGGAGAAT | 27342 |
| rs184030642 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716202 | TTTCCTTGCTTTGAG[C/G]TATAGTTTGTCTTAT | 27342 |
| rs184043477 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703435 | AGCTCTCACAGTTAG[A/G]TCTTTTATCCATTTT | 27342 |
| rs184046899 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802257 | GTGGGTAGAGGCCAA[C/G]GATTCTACTAAACAT | 27342 |
| rs184051692 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786865 | CCATTGCAAATGAGA[C/T]GGGCAGCTATGTCAT | 27342 |
| rs184075627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770569 | CCTCACTGCAGCCTC[C/T]AACTCCTGGGCTCAG | 27342 |
| rs184078897 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66753966 | TGCCTCTGCCTCCCA[A/G]AGTGCTGGGATTACA | 27342 |
| rs184086592 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741022 | AATCCTCAGAGTGCG[A/G]CCTCTCCGTCCCAGA | 27342 |
| rs184096019 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723861 | CTGGGATTACAGGTG[C/T]GAGCCACCATGCCTG | 27342 |
| rs184100089 | snp | C/G | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739724 | CCAAGAACACTACAG[C/G]GACAATTAGCAAAGC | 27342 |
| rs184208010 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693281 | TCATGTATGTTTCCA[A/C]CCCCCAGGGCACCAT | 27342 |
| rs184256314 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723746 | ACACCACGCCTGGCC[A/G]CTTTTGTATTTTTAG | 27342 |
| rs184303132 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783419 | TTTTGGCAAAGAAAA[C/T]ACTAATAGAACAACT | 27342 |
| rs184307119 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765976 | AAAAAACTTAATTGA[C/T]CTATACTTAAAAATA | 27342 |
| rs184312372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792151 | AAAGATGATCCCGTA[C/T]AATGATTAGAGAGTA | 27342 |
| rs184316878 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808051 | CTCTCGGAAGCACGT[A/G]ACATGTTATGTTGTT | 27342 |
| rs184369086 | snp | G/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755174 | TGGCAGGTGCCTGTA[G/T]TCCCAGCTCCTCTGG | 27342 |
| rs184380070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782827 | AAAAATTATTTTTTC[A/G]TTTTGGAAATCATTG | 27342 |
| rs184383193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747141 | ATAGCTCTCTTGGCA[A/G]TGGTCATTAAGAGGG | 27342 |
| rs184393231 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731643 | GATGGCTTGAGCCCA[A/G]GAGTTCGAGACTGCA | 27342 |
| rs184394560 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751887 | TCCTATTTCACTGGG[A/C]CCTTGAGTCCCAAAA | 27342 |
| rs184397639 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700357 | CCTGTGTAGGGTTGC[A/G]TTCCTGACATGCCAT | 27342 |
| rs184399948 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714174 | TTTGGTAAGAATTAT[A/C]TGGAGAAATTATCTA | 27342 |
| rs184409798 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718609 | AGGTTCAAGCTGCAA[A/C]TTCCTACCTGCACTC | 27342 |
| rs184500318 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798388 | GGAGTCCCAGGTTCC[A/G]GACAAGGGGCTGGTA | 27342 |
| rs184510271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765615 | CCTTCTACTTTTCTC[C/T]GCTTCTTGGGGTATG | 27342 |
| rs184518287 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680971 | GCCTATAATTCCGGC[C/T]ACTCGAGAGGCTGAG | 27342 |
| rs184526421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736251 | CCCTATCCCCAGAAA[A/G]TTACTATGGAGCACA | 27342 |
| rs184544812 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803431 | TTGGCTCTTTTCTTT[C/T]GTGATGTCCCAAGTT | 27342 |
| rs184555124 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787468 | TATGCCCCAGCCTCC[C/T]GCATAGCTGAGATTA | 27342 |
| rs184555209 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771517 | TTGGTGTCATATCCT[A/G]GAAGTCATTGCAAAA | 27342 |
| rs184587089 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66685875 | TGCAGAGCAAACATC[G/T]CTAGCAGAGATGACC | 27342 |
| rs184593995 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706446 | GACGGAGTCTCGCTC[C/T]GTCCCCAGGCTGGAG | 27342 |
| rs184601731 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797945 | AACGTGGTAAAACCC[C/T]GTCTCTACTAAAAAT | 27342 |
| rs184617518 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744356 | TGGGCAAAATAGCAA[C/G]ACTGCATCTCTACAA | 27342 |
| rs184622883 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782099 | CTTTCAAACACTAAA[G/T]AATTTTTTTCTAATC | 27342 |
| rs184625987 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764650 | TATGAAGTAAGCATC[C/T]AACATCTAACATCGT | 27342 |
| rs184627933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728050 | TCCAGTGTAATTCTT[C/T]GCAGACCCTCTGCCT | 27342 |
| rs184630593 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751186 | CAGACGTGCGCCACC[A/G]CACCTGGCTAATTTT | 27342 |
| rs184829918 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709021 | TATTTTAATTTTTTT[G/T]TTTTGTTTTGGTGAG | 27342 |
| rs184841722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794785 | ATTATTTATACCTAC[A/G]GTGCACAACAGTGAA | 27342 |
| rs184842196 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701107 | TGTTTGTGAGCAGCC[A/G]TGTGGCAGGTATGAT | 27342 |
| rs184842796 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777729 | GCCCAGGAGTTAGTG[A/G]CTGCAGTGAGCTCTG | 27342 |
| rs184843162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713596 | GAACATCCTTATCTT[A/G]TACCTTAACTTGGGT | 27342 |
| rs184847850 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760474 | TTGGAGACAGAGTCT[C/T]GCTCTATTGCCTAGG | 27342 |
| rs184857286 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747357 | GCTCTAAATTCTCTG[C/G]TGTTTCACCCTAAGG | 27342 |
| rs184866341 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732203 | GGTGCCTGGAGCACC[A/G]TCCATAAGCGAGCCC | 27342 |
| rs184894056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686605 | TAATCTAGACTGTTG[C/T]TATAATACGTAAACA | 27342 |
| rs184901586 | snp | A/C | 0.0490535 | 0.14873 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707028 | CTGGCCTCGTGATCC[A/C]CCCGCCTCGGCCTCC | 27342 |
| rs184919967 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798861 | CGGCTGCTTGGGAGC[A/C]TGAGGCAGGAGAATT | 27342 |
| rs184946122 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773875 | TTCACCATGTTGCCC[A/G]GGCTGGTCTCAAATT | 27342 |
| rs184964107 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743980 | GCTGCTATGTAGCTG[A/G]TAAGGATAAATGTTT | 27342 |
| rs184968457 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709091 | GGCACAATCTCGGCT[C/T]ACTACAACCTCTGCC | 27342 |
| rs185058955 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757906 | GTGAGCCACTGCGCC[C/T]GGCCGACCAAAACAT | 27342 |
| rs185071941 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690066 | TACAAGAAAACAACT[C/G]ATCAATATTGTTTAT | 27342 |
| rs185076386 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66809872 | GACTCGAGAAGTGTT[C/T]AGACAAACTCCCCTT | 27342 |
| rs185081904 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727788 | AGTCCAGGCATCGAT[C/T]ATGGAGGGCCTGACA | 27342 |
| rs185086349 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774634 | GTGTGGTGGTGTGCG[C/T]CTGTAGTCCCAATAA | 27342 |
| rs185087808 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66685261 | TGGGTTCAAGTGATT[C/T]GCCTGCCTCAGCCTT | 27342 |
| rs185088344 | snp | A/G/T | 0.00279258 | 0.0372817 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792706 | GATAGGTAGAAAGAG[A/G/T]TCTATGGAGAATTGT | 27342 |
| rs185096966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704750 | CAGGAGGCGGAGTTT[A/G]CAGTGAGCCGAGATT | 27342 |
| rs185100685 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758914 | TTTGGAACAATTAAT[A/G]ACTTCAAATCCATAG | 27342 |
| rs185100705 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721209 | CAGGCATGAGCCACT[G/T]TGCCCGGCCAAAAGA | 27342 |
| rs185108906 | snp | C/G | 0 | 0 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744659 | GGCGACAGAGCCAGA[C/G]TCCGTCTCAAAAAAA | 27342 |
| rs185114757 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728374 | CTGGGACTGAAATGA[A/C]GGTATCCCCCCTATG | 27342 |
| rs185205073 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754525 | ACAGTGGGCAGATCA[C/T]GTGAGCCCAGGAGTT | 27342 |
| rs185208712 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694140 | TGCTCTCCCTCTGCT[C/T]CAAGCCTGCAGAGAG | 27342 |
| rs185212603 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776364 | TTTATTAAAAGGAAA[G/T]ATTGCTCATAACCAA | 27342 |
| rs185219808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724420 | GTTGGAGTGCAGTGG[C/T]GCGATCTCGGCTCAC | 27342 |
| rs185320684 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794578 | CCAAATAAAAATTAT[C/T]AAGCCCAATGTTGTA | 27342 |
| rs185326695 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741534 | CTCAGCGCGGGTGAC[C/T]AATCCTTGCGGTTGG | 27342 |
| rs185328162 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760210 | TCGACACTCTTAACC[G/T]GGAAAAAGCACTAAT | 27342 |
| rs185331662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789133 | CCTTAAAATGACTCT[A/G]TTGTTGTAAACTATA | 27342 |
| rs185338009 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772738 | ACATGGTGAAACCCC[C/T]TCTCTACTAAAAATA | 27342 |
| rs185339151 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66755968 | ATTGACATTCACATT[C/G]ATTTTGGAAGCATTA | 27342 |
| rs185347152 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742666 | GGCTGGAGTACAGTG[A/T]CACGATCACGAGTCA | 27342 |
| rs185358194 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725009 | TCTTTTAAATCTTCT[A/G]TTTCTCTCCTTATTA | 27342 |
| rs185460932 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689268 | AGGTAGAATTAAAAC[A/T]TTTTTACAGGTCAGC | 27342 |
| rs185493436 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735742 | TGCTTTTCCTTCATC[C/T]TTCTGCCATGATTGT | 27342 |
| rs185553931 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808763 | AATACACAGAAGTTC[A/G]TGAGTTTGTTTTGTT | 27342 |
| rs185577259 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774127 | GCTAAAAAACCTTGG[C/T]TTCATTCTTGATTTC | 27342 |
| rs185592345 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810477 | CACTGATGTCTTTTA[C/G]AAACCAGGAGTTATC | 27342 |
| rs185628652 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718210 | AAATATTAGGCGTGG[G/T]GGTGCACATCTGTAA | 27342 |
| rs185724438 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801903 | AGACTTATTTATTTA[G/T]TTAGTTAGTTAGTTA | 27342 |
| rs185738747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769443 | CAAAGATTGAGATTG[C/T]GCTCAAACATCTCAA | 27342 |
| rs185842932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806036 | AGGCATGAGCCACCA[C/T]TCCTGACCTGAATTC | 27342 |
| rs185854762 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786326 | AAATTTCAGCACCTA[C/T]GTAATTTTCATACCC | 27342 |
| rs185864446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752153 | CAGTGAGCCATGATT[A/G]TGCCACTGCATTCCA | 27342 |
| rs185871369 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736839 | GCACTCCAGCCAGGG[A/C/T]GACAGAGCGAGACTC | 27342 |
| rs185876361 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66753353 | CCCAGAGTTCGATGT[A/C]AATTTGTGGAAAACT | 27342 |
| rs185884152 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694612 | AGCTGGAGGGGCAGG[A/C/G]CCCAGGAGCTAGTGA | 27342 |
| rs185900252 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682666 | CTCCCCGGAACGCGC[C/T]GGGATGGGACGCTCG | 27342 |
| rs185906616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702120 | TATATGGATTTGCCT[A/G]TTTGGATATTCATAT | 27342 |
| rs185934828 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785062 | CATGTATGCTGTATA[A/T]TATGTTTTAGAAAAT | 27342 |
| rs185956305 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752314 | AGCCTGGCCAACATG[C/G]TGAAACCCTGTCTCT | 27342 |
| rs185965097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707302 | AAGAATGTGTATCAT[A/G]TTGTTGTTGGGTAGG | 27342 |
| rs186043655 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703209 | TCATCTCCTGACCTC[A/G]TGCCCGCCCGCCTTG | 27342 |
| rs186070475 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799875 | TGGTTGTTAGAGAAG[C/T]GCTATGAGTTATTTT | 27342 |
| rs186082619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767096 | CAACCTCCATCTCCC[C/T]GGTTCATGCGATTCT | 27342 |
| rs186100788 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738363 | AACTTTGAAATGATA[C/T]TCAGTTTTTGTTACT | 27342 |
| rs186106386 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763253 | ACCTCAGGAGGTCAG[A/C]ATTAAGCATCGGCCA | 27342 |
| rs186112237 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748141 | AGACTTTCCAGCATG[C/T]GTTTCAAAGGGCTGG | 27342 |
| rs186120009 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732914 | CCCTGACCCCAGGCT[C/T]GCCCTGCTTCTCTAA | 27342 |
| rs186126429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715628 | ATTTTTTAGTGTTCT[A/G]TTATTGACTTCTAGT | 27342 |
| rs186164197 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682902 | GCCCATCACGGCAGT[C/T]TAGGGAGAGAGAGGG | 27342 |
| rs186216033 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795295 | GACGGACAAGGATCC[C/G/T]GTCTTTAGCTGAACT | 27342 |
| rs186221141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683280 | ATTGCGCGGCTTTAA[C/T]TGCTGTTAGTCTGTT | 27342 |
| rs186245224 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761656 | GACCCTCTCTGGGGA[A/G]GGTTTAAGACCAATC | 27342 |
| rs186255722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732777 | TCTCTCTTTCTCACT[C/T]GCTCTCTCTTGCTGT | 27342 |
| rs186282535 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686258 | TGCACTCCATCCTGG[A/G]CAACAAAGTGAGACT | 27342 |
| rs186316023 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799080 | GTCTTGGTAGCACTG[C/T]GTAATGTCATTTCAG | 27342 |
| rs186319421 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759493 | CATAGTATATTAGTT[C/T]GTTCATTCTCACGTA | 27342 |
| rs186330767 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745590 | TGGATCAAGATGGCA[A/G]AACTCCGTCTCTACT | 27342 |
| rs186332142 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783921 | ATAGTGCAACCTTGT[A/C]ATTTTATGCCTGAGA | 27342 |
| rs186338518 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766711 | TCCCACTGTTACCTC[C/T]TATTTATTTATTTAT | 27342 |
| rs186388644 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778386 | TGGAATGTCTTGACT[A/G]TAAAGACTCAGTTAA | 27342 |
| rs186411764 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747523 | GGTGATTTGGTCTGT[A/G]TGCTAAAATTAAAAA | 27342 |
| rs186425797 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715184 | CTAGGCTGGAGTACC[A/G]TGACAGGATCCTAGC | 27342 |
| rs186430020 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724446 | CTCACTGCACCCACC[A/G]CTTCCCAGGTTCAAG | 27342 |
| rs186455194 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706759 | ATTTTTCTAATTTAC[C/T]TTCTTCTTTGACATA | 27342 |
| rs186495604 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774877 | TCCTGTGTTCTCACA[A/G]CACTCAACTTTTACT | 27342 |
| rs186501912 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744963 | TTTGGGAAGCTGAGG[A/C]GGGTGGATCATGAGG | 27342 |
| rs186519371 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796661 | ACAGTGGTGTGACCT[C/T]GGCTCACTGCAACTC | 27342 |
| rs186533116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779806 | TATTTCCTACTTCTT[C/T]ACTTCTTTCATCTTA | 27342 |
| rs186536007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763546 | TATAATTCACATACC[A/G]TAGAATTCTCCCTTT | 27342 |
| rs186538416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748400 | GTAATGAATTTATCA[A/G]CAGTGGGGTTTGAGT | 27342 |
| rs186575779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711576 | TCTGTGGGTCTATTT[A/G]TATACTCTATTCTTT | 27342 |
| rs186643075 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689039 | GGGAGGTTGCAGTGA[A/G]CCGAGATTGCACCAC | 27342 |
| rs186658393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708767 | CAGTGAGGTATGATT[A/G]TACCACTGTACTCTA | 27342 |
| rs186691202 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792832 | GGCATGAGGATATGG[A/T]GGTGAACAGTGCCCT | 27342 |
| rs186709515 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759168 | CTGTAGTCACATCCT[A/G]TGTCAGCAGTCCCCA | 27342 |
| rs186721135 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729012 | CTGGAGTGCAGTGGC[A/G]CGATCTCGACTCACT | 27342 |
| rs186751445 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779234 | ATACGGCTGGCACAG[A/G]GGCTCACGCTTATGA | 27342 |
| rs186764895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793693 | TGTGCATGTATATGG[A/G]TAACTAGTTGACAGT | 27342 |
| rs186766989 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775635 | GAATTGAAATAGGTA[C/G]TTTTGCTTATGAAAT | 27342 |
| rs186767007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739776 | TCTCACAGCCACAGC[A/G]TAGTATTTTCTTTTT | 27342 |
| rs186775545 | snp | A/T | 0.167809 | 0.236103 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759724 | CGTTTAAACAACCAG[A/T]TCTCACAAGCACAGA | 27342 |
| rs186778041 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723759 | CCACTTTTGTATTTT[C/T]AGTAGTGACGGGGTT | 27342 |
| rs186785881 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745699 | TCTTGATCCCGGGAG[A/G]CGGAAATTGCAATGA | 27342 |
| rs186790914 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692646 | AGTTCTAAGTGGTGG[A/G]ACTGGGGAGTCAGAG | 27342 |
| rs186843439 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696061 | CCTTACAAGGGACTT[C/T]AAAATATATATATAT | 27342 |
| rs186897648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693029 | CCAGGCCCTCCTAGC[A/G]GGGGAAAAAAGCAGT | 27342 |
| rs186904086 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712555 | AGCCCACTGCAGCCT[C/T]GACCTCCCGGGCTGA | 27342 |
| rs186964768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796122 | AGCCTGGGCAACAGA[C/T]CGAGACTCTGTCTTC | 27342 |
| rs186983793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807004 | AGAGCGTTTTGGATT[C/T]AGTTCTTTATCCAAA | 27342 |
| rs186997516 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773839 | CCCAGCTAAGTTTTG[G/T]ATTTTATGTAGAGAC | 27342 |
| rs186999098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791542 | TTAAGCAGTTAACAG[C/T]AGTACAGACAAAACT | 27342 |
| rs187010660 | snp | C/T | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680486 | TGACCTCAGGTGATC[C/T]GCCCGCCTCTGCCTC | 27342 |
| rs187013624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699507 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCGTC | 27342 |
| rs187015778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757588 | ATATGTACCATATAC[A/G]GTAACTGCCTCTGGA | 27342 |
| rs187022845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743578 | GCGATCTCGGCTCAC[C/T]GCAAGCTCCCCCTCC | 27342 |
| rs187030546 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727397 | TGGCCACCCCATCCC[A/C/G]TGGCATTGCCTTCCC | 27342 |
| rs187031069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793441 | CCACTTGTGGTGTCA[C/T]GTCGACACTGACAAA | 27342 |
| rs187056265 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687557 | GGTGGCATGTTCCTG[C/T]AGTCCAAGCTACTCA | 27342 |
| rs187083863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737202 | CCCAAAATGCTGGTA[C/T]TACAGTATTTATTTA | 27342 |
| rs187101389 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785240 | CACTAGTTTATATCA[A/G]AGACCTGCATATGGC | 27342 |
| rs187113869 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767591 | TTCTAAACCACAAGG[G/T]GTTGCTACTAGGAGG | 27342 |
| rs187136535 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752408 | CTGAGGCAGGAGAAT[A/C]ACTTGAAACCAGAAG | 27342 |
| rs187136812 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737100 | AGCGAGAGCGAGAGA[C/G]AGAGAGAGAGAGAGA | 27342 |
| rs187143163 | snp | A/C | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66738820 | TGTAATCACAAAAGT[A/C]AGTTAAGAGCTTTAA | 27342 |
| rs187151547 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721797 | ACGTGGTAGAACCCC[A/G]TCTCTACTCAAAACA | 27342 |
| rs187212173 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811105 | TGTGAATCCAGATAT[A/G]CGGTCTTAATTCCTT | 27342 |
| rs187237753 | snp | C/T | 3.30153e-05 | 0.00406283 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66775323 | AGAAAAGAAAACCAA[C/T]GAGAAGACCCGCAAG | 27342 |
| rs187245095 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703712 | AGCTTTGTAAGTAAG[A/T]TTTGAAATTGGGAAA | 27342 |
| rs187260027 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694251 | GCATGGTAAGTAAAG[C/G]GTGCCACGGGAATGG | 27342 |
| rs187272835 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720267 | CAGTGGCGCGATCTC[A/G]GCTCACTGTAACCTC | 27342 |
| rs187334115 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797781 | GAATAGGGGGACTGT[C/G]TTCTTGGTCCATTAC | 27342 |
| rs187335701 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781613 | GCTGTGGTTCTACAC[A/G]TTACTTGGTGGTTTT | 27342 |
| rs187339532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764248 | ACATCTTTTCATATA[C/T]TCACGACTGTTTGCA | 27342 |
| rs187341323 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711102 | GAAGTTGAGGCTGCA[A/G]TGAGCTGTGATTGCA | 27342 |
| rs187351106 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750727 | AAAACTGATCAGCCA[A/G]TTGGACTACAGGTCC | 27342 |
| rs187353153 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803762 | GGCGTGGTGGTGCGT[C/G]CCTGTAGTCCCAGCT | 27342 |
| rs187355960 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734805 | GTCTTCAAAAATGAC[A/G]GACACTGCTGGTCGC | 27342 |
| rs187356292 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772519 | GTAGTAGAAATCTGT[G/T]GACTTGTATACATAG | 27342 |
| rs187361933 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717231 | CTAAGAATTACAGTA[G/T]GTACACCAAACTTTT | 27342 |
| rs187377496 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716594 | TGAAAGAGCAAGACT[A/C]TGTCTCAGAATAAAT | 27342 |
| rs187382970 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742527 | TGTCTTGAAGAATGA[C/G]TAACATTCAGACTAA | 27342 |
| rs187472016 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680276 | TTTGAGACAGAGTTT[C/T]GCTCTTGTTGCCCAA | 27342 |
| rs187477279 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698819 | GAGTTTCACTCCTGA[C/G]TCCACCCTGGTACTC | 27342 |
| rs187550875 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786694 | TAGGTGTGAGCCACC[A/G]CGCCCAGTGCTATTC | 27342 |
| rs187556485 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800963 | CCCGTTAAGTTACAC[A/C]GTGTGGGTCACGTTC | 27342 |
| rs187564176 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786154 | CATTTCTGTTTTCTC[C/T]AAGCCCTGTATATGC | 27342 |
| rs187571506 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66753623 | TCAGTTTGAAGAGCT[C/G]TCCCTGGTATTTCTT | 27342 |
| rs187592829 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730133 | AAGATGAAAAGAGCA[C/G]CACTTCCTCACGTCC | 27342 |
| rs187606287 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788255 | TTCGAGACCAGCCTG[C/G]CCAATATGGTGAAAC | 27342 |
| rs187624504 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734103 | TCTAACGGGGCCCTG[A/G]GGACACATTCATTCA | 27342 |
| rs187633209 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755439 | TGTGATCATGCCACT[C/G]CACTCTAGCCTGGGT | 27342 |
| rs187704872 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704025 | TTTGTTCAATTTATT[A/C]CTAAGTGTTTTATTG | 27342 |
| rs187772751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729888 | GTCTGTGCTGACTGG[C/T]TTGGCACCTGCAGCC | 27342 |
| rs187814947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802000 | CTGCAGCCTTGACCT[C/T]ACAGGCTCAAGCGAT | 27342 |
| rs187820078 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796992 | AGTTTTTTGCTGTGT[A/G]GACAGTGCTATGAAA | 27342 |
| rs187820699 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798313 | GAGGAAGAGACCACC[C/T]AAGTGTGGGAACAGG | 27342 |
| rs187826976 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764117 | GGTTCCAGTTTCCCC[A/G]CATTCTTGGCAACAC | 27342 |
| rs187829289 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769499 | CAGCAGAGCATGTGC[A/G]TACACAGAGGAGACA | 27342 |
| rs187830688 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782290 | TTCCTTTCTAGTTTG[C/T]CTCTTGCCCATCTAG | 27342 |
| rs187851694 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734575 | TGCTGAGATTACAGG[C/T]GTGAGCCACCATGCC | 27342 |
| rs187873268 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713434 | CGTCTAGCCCAACCT[A/G]TGGGATTTTCTATGG | 27342 |
| rs187954585 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688226 | TCCAACAAGAAGATA[G/T]AACAATTTAAACATA | 27342 |
| rs187988417 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684915 | GTTGGGATTACAGGC[A/G]TGAGCCACTGTATCT | 27342 |
| rs188010898 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743278 | TTGTACCAATGCACT[C/G]CAGCCTGGGCGACAG | 27342 |
| rs188022607 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726961 | GTGAGCCGAGATTGC[A/G]CCATTGCACTCCAGC | 27342 |
| rs188046739 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691682 | GAGAAATTCAACATT[G/T]TATTACAAAATAGGG | 27342 |
| rs188069524 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775996 | ATAACCAGCAAGAGG[A/G]TTGTCACTTAAGTCA | 27342 |
| rs188072768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794807 | AACAGTGAAAGAGGG[A/G]GAGCAACTCAAATGC | 27342 |
| rs188085912 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747039 | CCTCAGGTGATCCAC[A/C]TGCCTTGGCCTCCCA | 27342 |
| rs188091385 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777968 | GTAGAAAGCTTTGGG[G/T]ATAAAGACCTTAAAG | 27342 |
| rs188093588 | snp | C/T | | | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760485 | GTCTCGCTCTATTGC[C/T]TAGGCTGGAGTGCAA | 27342 |
| rs188104401 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781029 | TGTTTATAGCACGTA[G/T]ATTTAATGTGATTTT | 27342 |
| rs188106750 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713634 | TTCAGTCTTGAAGTA[G/T]GACTTTAGCTCTGGA | 27342 |
| rs188123869 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749171 | AGATCCAGATCTACT[C/T]GTCTCAGATGAAATG | 27342 |
| rs188138110 | snp | A/G | 0 | 0 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716946 | GCCATACCCCACTAA[A/G]TTTTGTATTTTTAGT | 27342 |
| rs188215078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683951 | TTGCTGCGTTGCCCA[C/T]GCTGGTCTTGAATTC | 27342 |
| rs188245311 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707810 | CGGTGCATATAGGCT[G/T]ACAAATGTTATATCT | 27342 |
| rs188295514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694483 | GGCCACAGAGGGCCC[A/G]GCGGGGCCTGGAGGG | 27342 |
| rs188324334 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810189 | GTGAGATGCAAGGGG[A/C]GCCTTGCAGCCTCCA | 27342 |
| rs188332515 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792744 | ATCTTATAAAGGGAG[A/G]AATGGTAATAAATGG | 27342 |
| rs188334324 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774754 | GATGGAGTGACACTC[A/T]GTCTCAAAAACAACC | 27342 |
| rs188340267 | snp | G/T | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758917 | GGAACAATTAATGAC[G/T]TCAAATCCATAGGAA | 27342 |
| rs188360738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789829 | CGTGGTGGCTCCATG[C/T]GTGAGGCTGGTGCCA | 27342 |
| rs188365959 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760109 | CTGACCAAGCAGGCC[C/T]GTCTGAGAATGTGCA | 27342 |
| rs188367798 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756273 | TGACAAAAAATTAAA[A/G]TTCGATAATGCTATG | 27342 |
| rs188382116 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731325 | AAGAGGAAGAAGGGG[C/G]TCACAGGAGAGGGTA | 27342 |
| rs188514987 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718668 | GTTCCCAAATACTTC[A/G]CAGTATTCAGATATG | 27342 |
| rs188516441 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709057 | AGTTTCACTCATGTC[A/G]CCCAGGCTAGAGCGC | 27342 |
| rs188608350 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769165 | GTTGGAAGAAAGTGG[C/T]AATCTCTTAGACAGC | 27342 |
| rs188662285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743158 | ACTAAAAACACTAAA[A/G]TTAGCTTGGTGTGAT | 27342 |
| rs188713034 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702936 | TAGGGTTTATTTTCA[C/G]TTTTTTGATAGTGTC | 27342 |
| rs188727261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802696 | AGAGGATGCTAGGAA[C/T]GGGTCTCTGCAGGAT | 27342 |
| rs188749790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787067 | AGTCTTGCTCTGTTG[A/G]CCAGGCTGGAGTGCA | 27342 |
| rs188756028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771284 | GCTGGGACTACAGGC[A/G]CCCGCCACCACGCCT | 27342 |
| rs188758017 | snp | A/G | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66753976 | TCCCAAAGTGCTGGG[A/G]TTACAGGCATGAGCC | 27342 |
| rs188760886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693919 | CTCAAGCGATTCTCC[C/T]GCCTCATCCACCAGA | 27342 |
| rs188762182 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715300 | ACCAGGCTAATTTTT[A/T]AAAAAATTTTTGTAG | 27342 |
| rs188772015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741165 | CCAGGCCGCTGGCTC[C/T]GAAGCAGCGTCTGTG | 27342 |
| rs188775536 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723896 | ATTATCTTTTAAAGA[A/T]ATGAAAATAAGAGAA | 27342 |
| rs188791335 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689595 | ATCACCTGAGGTCAG[A/G]AGTTAGAGACCAGCC | 27342 |
| rs188855977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806804 | GTGTGTCACCATGCC[C/T]GGCTAATGTTTGTAT | 27342 |
| rs188879322 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773567 | GGGAGTAAGACTAGA[C/G]AATTTGCATTTCTGA | 27342 |
| rs188904040 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752837 | GTTGTTTGCTGTTTA[A/C]TTTTTTTACTCCCAC | 27342 |
| rs188916576 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722277 | AAACCCCACCTTTAC[C/T]AAAAATACAAAAATT | 27342 |
| rs188980095 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798966 | TCAAAAAAGAAAGAA[C/G]TTGAGGACTGAGTGT | 27342 |
| rs188997273 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783601 | TTTAAATAACCTTAG[A/G]TAAGATACTTAAAGT | 27342 |
| rs189001175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766103 | CCCAGGACTTGGCAT[A/G]CTAAGTATAGGCTTA | 27342 |
| rs189014246 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752219 | AAAGTCTTGGCTGGG[C/T]GAGGTGGCTCACGCC | 27342 |
| rs189018343 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736927 | ATGCACAGACACCTA[C/T]GTATACAGACACACA | 27342 |
| rs189026911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719039 | CTCCAGCACTCTTGG[A/G]GCCACAGACTCTTGA | 27342 |
| rs189040351 | snp | G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681034 | TTTGCAGTGAGCCGA[G/T]ATCACACCACTGCAC | 27342 |
| rs189075631 | snp | C/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755176 | GCAGGTGCCTGTAGT[C/T]CCAGCTCCTCTGGAG | 27342 |
| rs189129042 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732464 | TTTAGGGGAGACTTT[A/C]CAGGTGAGAGGAGGC | 27342 |
| rs189137845 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777166 | GCTATGAAGAATACT[A/C]ATTCCTATTTAGCTT | 27342 |
| rs189144729 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790794 | AATGTGTTCTCTGAT[G/T]TTTAGTACCGCATGT | 27342 |
| rs189156125 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760237 | TAATTTGTCCTCCAT[A/G/T]TCTGTGGTTTTGTCA | 27342 |
| rs189162132 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747158 | GGTCATTAAGAGGGC[C/G]AAATACCATTATTAT | 27342 |
| rs189172582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756870 | TCCCCTTCCCCTCCT[C/T]CTTCTAACATTAAAT | 27342 |
| rs189177601 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714260 | AGTATGGGACTATTC[C/G]CATTCTCTGTTTTAC | 27342 |
| rs189217716 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681726 | ACTCGAACACCTGTC[A/T]CATCCTAGGATCCGC | 27342 |
| rs189226005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701472 | CCAGCACACTCCAGC[C/T]TGGAGGACAGAGCGA | 27342 |
| rs189255813 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803547 | GCTTGTTGGAAAAGG[G/T]TGGGCATTCATGAGA | 27342 |
| rs189332933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700707 | CCACCCACCCTAAGC[C/T]GTGCCCTCTGACCTC | 27342 |
| rs189340977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706921 | CGAGTAGCTGGGACT[A/G]CAGGCGCCCACGACC | 27342 |
| rs189348611 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805079 | ATAAAACATGATTTT[C/G]CTATTGCTTCTTTTT | 27342 |
| rs189371391 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798482 | GATGTGGAGCCCAAG[A/G]TCAGGAGCCAGAAGT | 27342 |
| rs189382041 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765881 | GATAACATGGGAGGT[C/T]ATGTGCTAGGCAGAC | 27342 |
| rs189388739 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774614 | TATTCAGCCTTATTA[C/G]TCAGGTGTGGTGGTG | 27342 |
| rs189392421 | snp | C/T | 0.0225045 | 0.103662 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758703 | CTCTCCTGCCTTCTA[C/T]CGTAACAGCTGTCAC | 27342 |
| rs189400194 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736436 | CTATAGACAGAAGAA[A/G]AAGGGGAGTGGTAAG | 27342 |
| rs189407309 | snp | C/T | 0.031825 | 0.122064 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744536 | AGCTGGGCATGGTGG[C/T]AGGCGCCTGTAGTCC | 27342 |
| rs189415333 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728160 | CTGGCTGTGGCCAGG[A/G]CCTTGCTTTGTTTCT | 27342 |
| rs189422937 | snp | A/C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714994 | TAGAAAACTTTCGTC[A/C/G]TCCTCCTCCTCCTCC | 27342 |
| rs189464764 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66685430 | GAGGCCAAGGTGGGA[C/G]AATCACTTGAGGCTA | 27342 |
| rs189476271 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704808 | AAAGTGAGACTCCGT[C/T]TCAAAAAAAAAAAAA | 27342 |
| rs189581788 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690502 | GGTGGATCACTTGAG[C/T]TCAAGAGTTCAAGAC | 27342 |
| rs189617865 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686449 | TGCACTACAGCCTGC[A/G]TGACAGAGTGATACC | 27342 |
| rs189635295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778485 | AGATACTTGCTTATA[C/T]ATTCCAAAGTGCCCT | 27342 |
| rs189645810 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755715 | CTGTTATTCCGGAGA[A/G]TGGCATGCTCAGATT | 27342 |
| rs189648223 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742537 | AATGACTAACATTCA[G/T]ACTAACAGGGTGGAG | 27342 |
| rs189650511 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783024 | GTGTGTTTATTTGAA[G/T]AGGGGAAAGAATTGT | 27342 |
| rs189652840 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747774 | AAAATGTTTATTAAT[C/T]GAAGAAAATGTTTTC | 27342 |
| rs189657960 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724610 | TGATCCACCCACCTC[A/G]GCCTCCCAAAGTGCT | 27342 |
| rs189667721 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751968 | TTGGGAAGCCAAGGT[A/G]GGAGGCTCACTTGAG | 27342 |
| rs189727666 | snp | C/T | 0.000572683 | 0.0169119 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796907 | GGTAAGTTTTTTTTT[C/T]AAGCGTATTTTTAAA | 27342 |
| rs189737210 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780866 | ACAACCACTTAAGCT[A/C]TTTTTCATTGTTTCA | 27342 |
| rs189780345 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693249 | GGCTGAATGGGTGGC[A/G]ATTGGAGACTTCACA | 27342 |
| rs189786784 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712672 | AGACAGGGTTTCACC[A/G]TGTTACCCAGATTGG | 27342 |
| rs189866099 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709276 | GAGTGCTGGGATTAT[A/T]GGTGTGAGCCATCGT | 27342 |
| rs189869265 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686150 | GCCAGGCATGGTGGT[G/T]TGTGCCTGTGATCTC | 27342 |
| rs189870039 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682680 | CCGGGATGGGACGCT[C/T]GGACCCAGACCACAG | 27342 |
| rs189892007 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752349 | AAAATACAAAAATTA[A/G]CCAGGTATGGTGGCG | 27342 |
| rs189892912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795820 | AACATTTAATAACTC[C/T]ATTGGGGCAGGGCTG | 27342 |
| rs189896484 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738449 | AACACTCATTCTGGG[C/T]CCAGGGGTCTAGGCT | 27342 |
| rs189903067 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761683 | AATCCAGAATAGAGT[A/C]CTGCCTTGGGGCAGG | 27342 |
| rs189907988 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721611 | CCCTCCTGCCTCCCC[C/G]CTTATGAGAAACTTT | 27342 |
| rs189917503 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792388 | CCAAAGACACGAGTC[C/T]CCTGGGTCAGAGACA | 27342 |
| rs189924687 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732805 | TGTCTCTCTCGCTTT[C/T]GCTCTCGCTCTCACT | 27342 |
| rs189942192 | snp | C/T | 0 | 0 | intron-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758438 | TGGGACCAATTGAAT[C/T]GTGCATTCTTTATGC | 27342 |
| rs189959086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727815 | GACAGGTCTGTGTTC[A/G]TGTTAACAATAGGAG | 27342 |
| rs190028795 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697471 | AGTGGCTCTGTCTGC[C/G]CATCCCAGCCGCCAG | 27342 |
| rs190044089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688432 | AATGGACATTTACAG[A/G]TACCCACCCAACAAC | 27342 |
| rs190132143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706458 | CTCCGTCCCCAGGCT[A/G]GAGTGCAGTGGTGTG | 27342 |
| rs190136574 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772917 | ACTCTGTCTCAAAAA[A/T]AAATAAATAAATAAA | 27342 |
| rs190138663 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789266 | TTATTGTGAGAACTT[C/T]AGCAGGGGTAGCAAC | 27342 |
| rs190152840 | snp | A/G | 0.000865801 | 0.0207882 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756094 | TGAGTACTGAAAGAT[A/G]TATAAGAAGAATATC | 27342 |
| rs190159024 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742852 | ACTCAAGCAATCTTC[C/T]TGCCTCAAGCGTCCC | 27342 |
| rs190174367 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808372 | AGGCGCCCACAACTG[C/T]GCCCAGCTAATTTTT | 27342 |
| rs190185177 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771804 | GATAATGGAATCACT[C/T]ACTTTTTGTTCATAA | 27342 |
| rs190189800 | snp | C/T | 0.0201999 | 0.0984476 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773970 | TGCACCTGGCCTGTG[C/T]TTGGGAATTAATACA | 27342 |
| rs190197432 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794590 | TATCAAGCCCAATGT[C/T]GTAAGGGCCATAGGG | 27342 |
| rs190199654 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741543 | GGTGACCAATCCTTG[C/T]GGTTGGGAAATGTGT | 27342 |
| rs190200158 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744004 | AATGTTTTCAGTGTA[A/G]TGCTTGATTATTTGC | 27342 |
| rs190294423 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692707 | CACCTAAAGCTCCCA[C/T]CCACCCCTCTCTGCA | 27342 |
| rs190368736 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800650 | AAAAGCCTGAATATG[A/G]ACCTGGGACTTGTGT | 27342 |
| rs190388338 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785691 | CATCCTGGCTATCAC[A/G]GTGAAACCTTGTCTC | 27342 |
| rs190392406 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767626 | GCCTTTGGGAGGTGA[G/T]TAGTTCATGAAAGTG | 27342 |
| rs190394856 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752643 | CTTTATAGCAGTGGT[C/T]CTCAAAGGTAGTTCC | 27342 |
| rs190407893 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66738938 | CTCCTCAGCACAGGT[A/T]CTTTGTGTTTTTTTG | 27342 |
| rs190409206 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695278 | AATTGTGCCACAGCA[C/T]TCCAGCCTGAGCAGC | 27342 |
| rs190429247 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787794 | GAGGGCAATTTTAAG[A/G]CACTGTATAGACCCA | 27342 |
| rs190430075 | snp | A/G | 1.65504e-05 | 0.00287662 | missense | RABGEF1 | GRCh38.p7 | 7:66809216 | CAACCGTTAGCAGCT[A/G]TTGACTCTGAAAACG | 27342 |
| rs190435675 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754737 | AAATCTGAATAAATA[C/T]ATTTCACGTCTAGGC | 27342 |
| rs190456015 | snp | A/T | 0.0759472 | 0.179459 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724425 | AGTGCAGTGGCGCGA[A/T]CTCGGCTCACTGCAC | 27342 |
| rs190479567 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751816 | CTTCCCTGTGTGGCT[A/G]TAGAATTTGGATTGT | 27342 |
| rs190500374 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718309 | GAGAACATGCCACTG[C/T]ACACTCCAGCCTGGG | 27342 |
| rs190541391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696587 | CCCAGCTATTTGGGA[A/G]GCTGAGGCAGGAGGA | 27342 |
| rs190682463 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683339 | CCAGAGATGCAAGAA[A/G]ATGTGATTATATTGT | 27342 |
| rs190683931 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788824 | GCTGGGCGTGGTGGC[A/G]GGTGCCTGTAATCCC | 27342 |
| rs190685787 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763595 | GACAGCCATTACCAC[A/C]GCCAACTTTAGAACA | 27342 |
| rs190692040 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682987 | CGAGTGACCAATCCT[G/T]GTGGTTGGGAAATGT | 27342 |
| rs190692543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703469 | TTATGATGTCAGGTA[A/G]AGATACATGAGGTGG | 27342 |
| rs190697726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792564 | ATTTAGGGATCCTTA[C/T]TAGACAGTAAGCAGT | 27342 |
| rs190701964 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734195 | CCATGCCCCAAACCA[C/G]AGAGTCCGGGGGCAG | 27342 |
| rs190728451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764885 | AGTAAGTTTTGAAAT[C/T]AGGAAATGTCAGTTT | 27342 |
| rs190740426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735856 | ACCCAGTCTCAGGCA[C/T]TTCTTTATAGCAGTG | 27342 |
| rs190804583 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796206 | TTTCCATCTTGGAAT[C/T]ACCATTTTGGTGAGT | 27342 |
| rs190806588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779293 | TGGATCACCTAAGGT[C/T]GGGAGTTCGAGACCA | 27342 |
| rs190820920 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763492 | CTCTAACTTCACATT[C/G]TGTCTCTTCTGTTTT | 27342 |
| rs190823034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748191 | GTGTTAGTAAAACTC[C/T]TTATTGGCTTTTTGT | 27342 |
| rs190832904 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732937 | TTCTCTAAACTTCTC[A/G]GCAGTCAGGGTGAGC | 27342 |
| rs190843186 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715646 | ATTGACTTCTAGTTA[A/T]ATTGTATGATCAGAA | 27342 |
| rs190928646 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686809 | ATTTTTATTTATAGT[A/G]GAACTTTTTTTTCTT | 27342 |
| rs190936091 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707142 | TTTGTGAGTTTTCCA[A/G]ATATCTTTGTTATTA | 27342 |
| rs190938564 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748710 | GTCCTGAAGCAGGGA[C/T]GCTATGAGAGAGGAG | 27342 |
| rs190940196 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800582 | ATGACTACTCTGCCC[C/G]CCGCACCTTTTGCTC | 27342 |
| rs190949125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772707 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGACCA | 27342 |
| rs190951466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767445 | ACCCCAAAAAACTTT[C/T]TCGTGCTAATCCTTT | 27342 |
| rs190952121 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703219 | ACCTCGTGCCCGCCC[A/G]CCTTGGCCTCCCAAA | 27342 |
| rs190961438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716643 | GCAGCAACAAAATGT[A/G]TAGTCATGTCTTTTT | 27342 |
| rs190980691 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744716 | AATGTATACTCATTT[C/G]CTAGTTGTTTCTTTC | 27342 |
| rs191054343 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775615 | GTTTATAGGAGGAAT[A/C]AAGAGAATTGAAATA | 27342 |
| rs191058350 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793502 | ATTTTTGGGTTAGGA[A/G]TGCTCAAATCTGTAG | 27342 |
| rs191060632 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799695 | TCTTTTTTTTGTACT[A/T]CTTTTTTTATTTAGT | 27342 |
| rs191070755 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759494 | ATAGTATATTAGTTC[G/T]TTCATTCTCACGTAG | 27342 |
| rs191083987 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730009 | GAAATCAGGAAATTC[A/C]AGTAGGAGGGAAGAG | 27342 |
| rs191125453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798326 | CCCAAGTGTGGGAAC[A/G]GGGCCAAGGCTGAGC | 27342 |
| rs191179720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785114 | TTTTCTTTTGCTCAG[A/G]AGTGTGATGTGTTCT | 27342 |
| rs191235962 | snp | A/C/G/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728384 | AATGAAGGTATCCCC[A/C/G/T]CTATGGCTGGGTCAG | 27342 |
| rs191247189 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725607 | ATGTTATGCTGTTTT[A/T]GTTCCATCCATGGCA | 27342 |
| rs191306390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773603 | TGCCTGGTGATGCTG[C/T]GCTGCTGTCTGGGGA | 27342 |
| rs191312812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756988 | ACTAGTTTGCAAATA[A/G]AAATTCAGAAAATTA | 27342 |
| rs191333176 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727128 | GTGTGAATTTTATTA[A/C]AATAAAGCTATTCTT | 27342 |
| rs191431521 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797111 | TCGAGACCAGCCTGG[C/G]CAACATGGTAAAACC | 27342 |
| rs191470807 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793011 | ACTGCAGTAGAAATA[C/G]AAAAGGAGTTTTCGG | 27342 |
| rs191480182 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711748 | CCTGACACCATGCCC[A/G]GCTAATTTTTTGTAT | 27342 |
| rs191496719 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759388 | TGCTTACTTCCCCAG[C/G]CGTAAACTCTAGCAA | 27342 |
| rs191500677 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687978 | TAATCCCAGCTACAC[A/G]GTAGGCTGAGGCAGG | 27342 |
| rs191509977 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729524 | ACCTCACCTTTATCC[A/T]CACCTTCAACCTCAC | 27342 |
| rs191550188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770380 | TGAACGGAAATTGTT[A/G]CATAGCGATTTACCA | 27342 |
| rs191555143 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793874 | TGTATCGGCCCTTGG[C/T]GTGTGAGGTCAGTGG | 27342 |
| rs191565532 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66753933 | GCTGTTCTTGAACTC[C/T]TGACCTTGTGATCCA | 27342 |
| rs191573926 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739886 | CTTACATGGGAATCA[C/T]GTAAAGAATCAGGTA | 27342 |
| rs191573971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775928 | GTAGCTATTTTCCAG[C/T]GCATGGATTTGTATG | 27342 |
| rs191579026 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723829 | AGGTGATCTGCCCAC[C/T]TTAGCCTCCCAAAGT | 27342 |
| rs191714111 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810628 | TTATCTCAGTGGAAC[C/G]TTCTATAACCTAAAT | 27342 |
| rs191719205 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734715 | TGGGATTACAGGTGT[A/G]AGCCACCGTGCCTGG | 27342 |
| rs191731560 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806145 | GGGCAGCGTATGGAC[C/T]TGGTTTTCTGTGTTG | 27342 |
| rs191732526 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716968 | ATTTTTAGTAGAGAC[A/G]GGGTTTCGCCATGTT | 27342 |
| rs191736280 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774975 | AGCTTGTTAGGGAAA[A/T]GGATTAGACTTGATT | 27342 |
| rs191749770 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773483 | TGTGACCCTGCTAAA[A/T]CTCTCGGAAAGCTTG | 27342 |
| rs191759384 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743178 | CTTGGTGTGATGGCG[C/G]CTGCCGTAATGCTAG | 27342 |
| rs191762175 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745261 | CTAAAATTCTGTTTA[C/T]TTATGTGAGTCTTTG | 27342 |
| rs191764350 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707514 | CCAATATGGGGAAAC[C/G]CTGTCTCTACTAAAA | 27342 |
| rs191770054 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807321 | GAACCCCACGGGCAC[C/T]CACAGTCTTCATCTT | 27342 |
| rs191776456 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694367 | GCAGCAGTGATGGTC[A/C/G]GGAGAAGATGGAGCG | 27342 |
| rs191777513 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791687 | TGGAAACAAAGATCT[C/T]AGCCAGACTGTTAAG | 27342 |
| rs191778728 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773863 | TAGAGACAGGGTTTC[A/G]CCATGTTGCCCAGGC | 27342 |
| rs191783439 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757801 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 27342 |
| rs191967044 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811379 | GAAGATGTTGGTATT[A/T]TATGTAGGGTAAATG | 27342 |
| rs191987271 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714173 | CTTTGGTAAGAATTA[A/T]CTGGAGAAATTATCT | 27342 |
| rs192001385 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784538 | GTAACATTCTATAAC[C/G]ATTAAACTCAGAATT | 27342 |
| rs192013022 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752269 | GAGTCCGAGGTGGAC[A/G]GATCACAACAAGGTC | 27342 |
| rs192015030 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698104 | TCACAGCCACGCACC[A/C]CCCCCACCCTCAGAC | 27342 |
| rs192024871 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720355 | GGCATGCACCACCAC[A/G]CCCAACTAATTTTTG | 27342 |
| rs192025202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790325 | GTTCCACCCTTATGC[A/G]CATGAGGTCTTTTTT | 27342 |
| rs192026896 | snp | C/G | 0.00676609 | 0.0577691 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680277 | TTGAGACAGAGTTTC[C/G]CTCTTGTTGCCCAAG | 27342 |
| rs192033477 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699343 | TTGCCTTTCACCAGA[A/T]ATAAGGCATTGGGCA | 27342 |
| rs192058340 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692282 | CTCTGCTGCTCATTA[A/G]CGGACCCTTTCTTTG | 27342 |
| rs192070974 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726695 | TTTTGTTTTCAGGAT[A/G]ATGAAATGGTCTAAA | 27342 |
| rs192187782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764932 | AGTATTGTTTTGGCC[A/G]TTCTGGGCCCTTGTT | 27342 |
| rs192200228 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790994 | CTGTGTGTCTCTTGT[A/G]CAACTTGTAACATGG | 27342 |
| rs192205898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736045 | TTAGCATTGCACTGG[A/C]GATCCTAGCCAATGC | 27342 |
| rs192219443 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797839 | ATCGGTATCAAGGCA[A/G]GGGATGTCGGCTGGG | 27342 |
| rs192235127 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781778 | CAAATTCTGGTCACA[C/T]TGGCCTCCGTGAACT | 27342 |
| rs192237240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764508 | CCTGCTTTTGGTGCC[A/G]TATCTAAACATCCTT | 27342 |
| rs192251823 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751179 | GGAATTACAGACGTG[C/T]GCCACCGCACCTGGC | 27342 |
| rs192255357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735315 | TCACTCCAGCATCAC[A/G]CTATTAAATGACTGT | 27342 |
| rs192262086 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684999 | CCAACCCCTGGCCTC[A/G]AGTGATTCTCTAGCC | 27342 |
| rs192267226 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717585 | AGTATGGTGAAACCC[C/T]GTCTCTAGTGTCACC | 27342 |
| rs192338054 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766887 | GCGCCACCATGCCTG[G/T]CTACCCACTGTGTTA | 27342 |
| rs192365432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737700 | CACATTCTCAACAAC[A/G]GCAAAATAGCAGCCA | 27342 |
| rs192371051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66685524 | TCTTGAAGTGAATGT[A/G]TACTCATTTCCTGGT | 27342 |
| rs192382827 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705449 | CTCGAAAGAAAGAGA[A/G]AGAGAGAGAGAGAGA | 27342 |
| rs192424575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802066 | AGGCACGTGCCACCA[C/T]ACCCAGCTAATTTTT | 27342 |
| rs192477627 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777225 | AAATGATAAGTATTT[A/G]TGATAACAGATGAAA | 27342 |
| rs192478292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794734 | CACTTTTGGAAATGT[A/G]TGACAGAGAACCGAA | 27342 |
| rs192489163 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745843 | CTCATGCCTATAATA[C/G]CAGTGCTTTGGGAGG | 27342 |
| rs192490952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760320 | TTAGAAAACTCAACA[C/T]GTTGCTCTTGTGTTA | 27342 |
| rs192493127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747161 | CATTAAGAGGGCCAA[A/G]TACCATTATTATGAT | 27342 |
| rs192503989 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713555 | TTTGGTCTTCCAGTA[C/G]AATGTTGAACAGGAG | 27342 |
| rs192505699 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731907 | TCAAGGTTCATCCGA[C/T]GCCCCTGAGATGTGC | 27342 |
| rs192537807 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680960 | TGGTGGCGGGCGCCT[A/G]TAATTCCGGCTACTC | 27342 |
| rs192579049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782682 | TACTCGGAGACTTGA[A/G]TAGCTCAGTAGGAGA | 27342 |
| rs192580680 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806864 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAA | 27342 |
| rs192581529 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689047 | GCAGTGAGCCGAGAT[A/T]GCACCACTGCATTCC | 27342 |
| rs192586338 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708812 | GCAAGACCCTGTCTC[A/G]AAAAAAAATTTACAA | 27342 |
| rs192602576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751861 | ACCAGCCTCCTCCCC[A/G]GATCTTTGACTCCTA | 27342 |
| rs192618292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718416 | TCCAACATCTGTGCC[A/G]TCTTGGGGTTGGCAT | 27342 |
| rs192683223 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704599 | GTGGATCACGAGGTC[A/G]GGAGATCGAGACCAT | 27342 |
| rs192717228 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781032 | TTATAGCACGTATAT[G/T]TAATGTGATTTTTGA | 27342 |
| rs192726011 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749659 | AGCCTGGGCAACAAA[A/G]CAAGACTCCATCTCT | 27342 |
| rs192742416 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703930 | TCTATGAACATGGGA[C/T]GCTTTCCCATTTATT | 27342 |
| rs192772450 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786817 | ATGTATACTCTTACA[A/G]TACTTCTATACATTC | 27342 |
| rs192790774 | snp | C/T | 0.167809 | 0.236103 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759725 | GTTTAAACAACCAGA[C/T]CTCACAAGCACAGAA | 27342 |
| rs192800187 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730473 | CATAGCTCACTGCAG[C/T]GTCAACCTCCTGGGC | 27342 |
| rs192825699 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700320 | TCGGCCTGAGCTCCT[C/T]TTTCGCCTTGAAGGG | 27342 |
| rs192829277 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794252 | ATTATTGTTAAAAAA[A/T]TTTTTTAATTTCTTT | 27342 |
| rs192839351 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760122 | CCCGTCTGAGAATGT[A/G]CATCATTTGAGCAAC | 27342 |
| rs192881949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689915 | TGGCTTTACCAGTGA[C/T]TTCTACCAGACATTT | 27342 |
| rs192919161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743584 | TCGGCTCACTGCAAG[C/T]TCCCCCTCCTGGGTT | 27342 |
| rs192924426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764233 | GACTGATGATGTGGA[A/G]CATCTTTTCATATAC | 27342 |
| rs192946652 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684231 | CGGTTGGATCACGAG[G/T]TCAGGAGTTCAAGAC | 27342 |
| rs192956636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808489 | AAAGTGCTGGGATTA[C/T]AGGCTTGAGGCACCG | 27342 |
| rs192959270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774009 | ACATGCAGCTAATCC[A/G]AAGCCAAATTTATTG | 27342 |
| rs193043492 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776363 | TTTTATTAAAAGGAA[A/G]TATTGCTCATAACCA | 27342 |
| rs193067163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722168 | TCTCAGGGGCTGGGT[A/G]CGGTGGCTCACGCCT | 27342 |
| rs193099024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709087 | CAATGGCACAATCTC[A/G]GCTCACTACAACCTC | 27342 |
| rs193099294 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786226 | AAATTAAATCTTTTC[C/T]GAACTGCATTAAAAT | 27342 |
| rs193101362 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66753306 | TGGGGTGTATGATTG[C/T]CCTATTTGTAAAGAA | 27342 |
| rs193107309 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723412 | CACAATCTACCCTTA[C/T]GTTGCGTTTAACACT | 27342 |
| rs193125376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700884 | CTGGCCCTGTCCAGA[C/T]TCTCATACTGTGGGG | 27342 |
| rs193180203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792480 | GTATCTGTTCCTATA[A/G]GATAATGCAGAGAAG | 27342 |
| rs193207167 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693954 | TTGGGATTACAAGAA[C/T]GTTCCACTACGTTTG | 27342 |
| rs193253458 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801608 | TTTTAAGTGTTTAGC[C/T]CCCACCAATGAGTGA | 27342 |
| rs193255513 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769320 | CCCAGCAACTGCAGT[C/G]GCTGTGCTCAGTTTT | 27342 |
| rs193259746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739484 | CATGGTGAAACCCTG[C/T]CTCGACTAAAAATAC | 27342 |
| rs193277392 | snp | G/T | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681168 | GGGATTCCAACCCAG[G/T]TCTATCTAAGAGCCA | 27342 |
| rs199511055 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720196 | ATTATTATTATTATT[-/A]TTTTTTTTTTTTTCT | 27342 |
| rs199601693 | in-del | -/A | 0.137187 | 0.223099 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710979 | ACTACAAAAAAAAAA[-/A]TAATAAAGGAAATAA | 27342 |
| rs199602650 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763811 | GTAGCATATATCAGC[A/C]CTTCATTCCTTTTTA | 27342 |
| rs199607958 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724366 | GTATTTATTTATTTT[-/A]TTTTTTTTTTTTGAG | 27342 |
| rs199616029 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699703 | TCTCAAAAAAAAAAA[A/C]CAAAACTGGTGTGGT | 27342 |
| rs199624630 | snp | A/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754387 | TTTTTTTTTTTTTTT[A/T]AAGCCATCATACTTT | 27342 |
| rs199627935 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752193 | CAGACTCTGTCCCAA[-/T]TTAAAAAAAAAAAGT | 27342 |
| rs199632155 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811188 | GCATATCAACTTCCC[-/A]CAAAAGCTGACTTTT | 27342 |
| rs199657509 | in-del | -/CCACCC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728774 | CCGCCATCCTCACCT[-/CCACCC]TCACCTTCACCTCCA | 27342 |
| rs199723632 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799681 | TTTTTTCTTTTTTTT[-/T]GTACTTCTTTTTTTA | 27342 |
| rs199734132 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712823 | TTCCTTTTTTTTTTT[-/T]GACAGGGTCTTGCTT | 27342 |
| rs199760522 | snp | A/G | | | intron-variant, utr-variant-5-prime | RABGEF1 | GRCh38.p7 | 7:66768882 | TTTCCACCACTGCCT[A/G]CACATTTGAGACCAA | 27342 |
| rs199762976 | in-del | -/G/TG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773082 | TCTAGCTAGTTGTTT[-/G/TG]GTTTTTTTTTTTTCA | 27342 |
| rs199804917 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793427 | AGGTGTGGAATTTCC[C/T]ACTTGTGGTGTCATG | 27342 |
| rs199810095 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728785 | ACCTCCACCCTCACC[C/T]TCACCTCCATCCTCA | 27342 |
| rs199819603 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760604 | GCATGCCATCATGCC[C/T]GGCTAATTTTTGTAT | 27342 |
| rs199838599 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783551 | ATTCAAACATAAAAT[G/T]ATTTAAATTCAAGTT | 27342 |
| rs199864371 | in-del | -/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738014 | TTGGTTGTGTTTTTT[-/G]TTTTTTTTGTTTTTT | 27342 |
| rs199878577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745494 | ACCATAGGCTGGGTG[C/T]GGTGGCTCACACCTG | 27342 |
| rs199881006 | in-del | -/TGTGTGTG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702348 | GGCTATTGTTTTGTT[-/TGTGTGTG]TGTGTGTGTGTGTGT | 27342 |
| rs199906815 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713783 | TGATACGTTGATATG[A/G]TCATATTGATATATT | 27342 |
| rs199909175 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745191 | CAAAAAAAAAAAAAA[-/A]TGATATCAGTACTTA | 27342 |
| rs199912713 | in-del | -/G | 0.0689305 | 0.172377 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796249 | AGTTTAAAAAAAAAA[-/G]AGCTTCAAGTTTTTA | 27342 |
| rs199938845 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737218 | TACAGTATTTATTTA[A/G]TTTTTAGGTGTTTTT | 27342 |
| rs199942603 | snp | C/G | | | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757283 | TTCTAACTTGTTATT[C/G]TTTCTCTGTTACAAG | 27342 |
| rs199950237 | in-del | -/ATTTTTT | 0.031825 | 0.122064 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771633 | GTGAGTCCTTTCTTA[-/ATTTTTT]ATTTTTTATTTTTTA | 27342 |
| rs199965735 | in-del | -/T | 0.231775 | 0.249335 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706779 | TCTTTGACATACTGG[-/T]TTTTTTTTTTTTTTT | 27342 |
| rs199968128 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706930 | GGGACTACAGGCGCC[A/C/T]ACGACCACGCCTGGC | 27342 |
| rs199988808 | in-del | -/T | 0.346147 | 0.230772 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782466 | GTGTACATACCTTAC[-/T]TTTTTTTTTTTTTTG | 27342 |
| rs200039143 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749824 | AAATATTTTAAAAAA[-/A]TTAGCTGGGTGTGAT | 27342 |
| rs200080284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767049 | CCTCTGTTGCCCAGG[C/T]TGGAGTGCAATGGCA | 27342 |
| rs200112167 | snp | A/G | 0.000148394 | 0.00861248 | missense | RABGEF1 | GRCh38.p7 | 7:66809040 | GCGTCAAGCAAATGT[A/G]TAAGAACTTGGATCT | 27342 |
| rs200120070 | snp | C/G/T | 0.000980832 | 0.0221239 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775402 | AAGAAGGGTAATGTT[C/G/T]TGATACTCTTTTTTT | 27342 |
| rs200122784 | snp | C/T | 0.00199802 | 0.0315439 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805129 | GAAATATTGTCTTTT[C/T]TGCTTTGTAGATATC | 27342 |
| rs200124555 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720188 | TTATTATTATTATTA[-/T]TTATTATTTTTTTTT | 27342 |
| rs200131535 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734018 | TCAAAAACAAAAAAC[-/A]AAAAAAACCTCCTAG | 27342 |
| rs200179936 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721164 | GCTCAAGTGATCTGC[C/T]GGCCTCGGCCTCCCA | 27342 |
| rs200210612 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796249 | AGTTTAAAAAAAAAA[A/G]AGCTTCAAGTTTTTA | 27342 |
| rs200225436 | in-del | -/ATT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720170 | ATTCAACATCCATTC[-/ATT]ATTATTATTATTATT | 27342 |
| rs200241241 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713144 | TTTTTCTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 27342 |
| rs200360503 | snp | C/T | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680523 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCACC | 27342 |
| rs200381594 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689802 | CAAAAAAAAAAAAAA[-/A]GAAAATAGGGGTAAA | 27342 |
| rs200392169 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699698 | TTCCATCTCAAAAAA[A/C]AAAAACAAAACTGGT | 27342 |
| rs200396409 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733983 | GCACTCCAGCCTGGG[C/T]GACACAGCGAGACTC | 27342 |
| rs200401069 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785754 | TGGCAGGCGCCTGTA[A/G]TCCCAGCTACTTGGG | 27342 |
| rs200418249 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772921 | TGTCTCAAAAAAAAA[-/T]AAATAAATAAATAAA | 27342 |
| rs200458734 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729398 | TTCTCACTCACTGTC[A/C]CTCTTTCACCTCCAT | 27342 |
| rs200462536 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774572 | TTGTAGTTCCTTCTT[C/T]CTGGAATGTCCTTTC | 27342 |
| rs200489206 | in-del | -/C | 0.0162398 | 0.0886349 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721976 | GACAATATAGTGAGA[-/C]CCCCCCCTCCGTCTT | 27342 |
| rs200519562 | in-del | -/A | 0.0839998 | 0.186933 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782785 | GTCTCAAAAAAAAAA[-/A]TAAAACATACTTTTA | 27342 |
| rs200557777 | in-del | -/TA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720193 | TATTATTATTATTAT[-/TA]TTTTTTTTTTTTTTT | 27342 |
| rs200599982 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699704 | CTCAAAAAAAAAAAA[A/C]AAAACTGGTGTGGTA | 27342 |
| rs200612883 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728736 | CACCTCCACCTTCAC[C/T]TCCATCCTCACCTCG | 27342 |
| rs200751177 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811189 | CATATCAACTTCCCA[-/C]AAAAGCTGACTTTTT | 27342 |
| rs200792697 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723629 | CTTGTTGCCCAGGCT[G/T]GAGTGTAGTGGTGTG | 27342 |
| rs200798351 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720191 | ATTATTATTATTATT[A/T]TTATTTTTTTTTTTT | 27342 |
| rs200803608 | in-del | -/TTTTC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713130 | CTTGGGATTTTCTTT[-/TTTTC]TTTTCTTTTCTTTTT | 27342 |
| rs200860280 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743085 | GAGGCCGAGGCGGGC[A/G]GATCACGAGGTCAGG | 27342 |
| rs200877189 | snp | A/C | 7.10795e-05 | 0.0059611 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772095 | TAAAAGGACTTAACT[A/C]GGGGCGGTTGAACAG | 27342 |
| rs200887434 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785781 | TGGGAGGCTGAGGCA[A/G]GAGAATGGCGTGAAC | 27342 |
| rs200891313 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784293 | ATAGAATTTAGACAA[-/T]GAAAGGGACTTTAGC | 27342 |
| rs200902240 | in-del | -/A | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754004 | CCAACGTACTAGGCC[-/A]ATTTTTTTTTTTTTT | 27342 |
| rs200920841 | in-del | -/AA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792111 | GCGAGACTCCATCTC[-/AA]AAAAAAAAAAAAAAG | 27342 |
| rs200933003 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724364 | AGTATTTATTTATTT[-/A]TATTTTTTTTTTTTG | 27342 |
| rs200951609 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773015 | GCCAGAGCATTCTAG[-/A]AATTCTAAAACTGCT | 27342 |
| rs200973754 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687500 | AAAAAAAAAAAAAAA[A/G]AAAGAAAAAAGAAAA | 27342 |
| rs200992256 | in-del | -/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738019 | GTGTTTTTTGTTTTT[-/G]TTTGTTTTTTTTTTT | 27342 |
| rs201014697 | in-del | -/TTTTCT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744037 | TTTTCTTTTCTTTTC[-/TTTTCT]TTTTTTTTTTTTTAA | 27342 |
| rs201058600 | snp | C/T | 0.00199804 | 0.0315441 | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66809014 | GAGTTGGTCTCCTGA[C/T]GCTTGCTTAGGCGTC | 27342 |
| rs201062667 | in-del | -/T | 0.0267878 | 0.112589 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707360 | TTGGCATACATTCTG[-/T]TTTTTTTTCTGATCT | 27342 |
| rs201075125 | in-del | -/AG | 0.0240643 | 0.107019 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730333 | TCCTCATCTATCGAC[-/AG]GGGATAAACAATAGG | 27342 |
| rs201113954 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698336 | ATCAGAACCCCCAGG[A/G]CAAGGCCTGTCTCCC | 27342 |
| rs201177885 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746331 | CTTTTTGAGACGGAG[C/T]CTTGCTCTGTTGCCC | 27342 |
| rs201189339 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710959 | ACCAGCCTGGGCAAC[A/G]TAGCGAGACCCTGTC | 27342 |
| rs201200930 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784317 | CTTTAGCAACTATGG[A/T]GTTTCAGTCCCTTTA | 27342 |
| rs201210820 | in-del | -/TGTGTGTGTGTGTGTG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702348 | GGCTATTGTTTTGTT[-/TGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 27342 |
| rs201218210 | snp | A/C | 0.079617 | 0.182947 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699699 | TCCATCTCAAAAAAA[A/C]AAAACAAAACTGGTG | 27342 |
| rs201223322 | snp | C/T | 3.31411e-05 | 0.00407056 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805422 | GAGTTCTTGGTGTTG[C/T]GGAGAAGGACTAGGA | 27342 |
| rs201266229 | in-del | -/CAG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716626 | AATAAATAAATAAAA[-/CAG]CAGCAACAAAATGTA | 27342 |
| rs201292499 | in-del | -/TTT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720195 | TTATTATTATTATTA[-/TTT]TTTTTTTTTTTTCTT | 27342 |
| rs201310190 | snp | A/T | 0.0603597 | 0.1629 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724365 | AGTATTTATTTATTT[A/T]ATTTTTTTTTTTTGA | 27342 |
| rs201344047 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715063 | TCCTTCTCTTTCTCT[C/T]TTTCCTTCTCTTTCT | 27342 |
| rs201344265 | in-del | -/G | 0.368119 | 0.220336 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764392 | AAATGACTTGCAAAT[-/G]TTTTCTCTTATTCTG | 27342 |
| rs201389633 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793006 | CATAAACTGCAGTAG[A/G]AATAGAAAAGGAGTT | 27342 |
| rs201418385 | snp | A/T | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680546 | ACCGCACCCAGCCAT[A/T]CTTTTGTTTTATACT | 27342 |
| rs201420649 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743326 | AAAAAAAGAAAAAAA[-/T]TTAAAAAAAAAAAAA | 27342 |
| rs201470152 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713369 | TCCTGACCTCGTGAT[C/T]GGCCCGCCTTGGCCC | 27342 |
| rs201491869 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766391 | TCATGATTTCTTAAT[G/T]TTAGTATCTTTATCT | 27342 |
| rs201493826 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728761 | ACCTCGACCCTCACC[G/T]CCATCCTCACCTCCA | 27342 |
| rs201507468 | snp | A/T | 0.0603597 | 0.1629 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724366 | GTATTTATTTATTTT[A/T]TTTTTTTTTTTTGAG | 27342 |
| rs201539921 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720194 | ATTATTATTATTATT[-/A]TTTTTTTTTTTTTTT | 27342 |
| rs201553504 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744041 | CTTTTCTTTTCTTTT[C/T]TTTTTTTTTTTTTTA | 27342 |
| rs201560671 | in-del | -/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761887 | GAAACCCCATCTCTA[-/C]CTAAAATACAAAAAT | 27342 |
| rs201596547 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728741 | CCACCTTCACCTCCA[C/T]CCTCACCTCGACCCT | 27342 |
| rs201618912 | in-del | -/CTA | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687811 | CAAATGAGGCCAGGC[-/CTA]TTAGTGACTCATGCC | 27342 |
| rs201620025 | in-del | -/TC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773095 | TTTGTTTTTTTTTTT[-/TC]ATCCAGTCAGCCAAT | 27342 |
| rs201638898 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751907 | GAGTCCCAAAAGTCA[A/G]AATCTTAGGCTGGGC | 27342 |
| rs201679519 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725966 | ATCCCACTTAGAAAA[C/G]CCCCATTCATCAGGC | 27342 |
| rs201695062 | snp | C/T | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680547 | CCGCACCCAGCCATA[C/T]TTTTGTTTTATACTC | 27342 |
| rs201695839 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770791 | CCCAGCCTGGGTTTG[-/T]TTTTTTTTTACAGTA | 27342 |
| rs201725781 | snp | G/T | 0.067446 | 0.170804 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706787 | ATACTGGTTTTTTTT[G/T]TTTTTTTTTTTTGAG | 27342 |
| rs201758679 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701517 | TTTTTTTTTTTTTTT[A/T]AATTTTTTGAGACAG | 27342 |
| rs201770270 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720507 | CCACCCCACTGATAA[A/T]TAAAAAAAAAAAAAA | 27342 |
| rs201775603 | in-del | -/TG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738013 | CTTGGTTGTGTTTTT[-/TG]TTTTTTTTGTTTTTT | 27342 |
| rs201807043 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784072 | GTGGAAATTCTGACC[-/T]TGAAGCCACTTGAAT | 27342 |
| rs201838145 | in-del | -/TTTTTTTTTTTTTTTTTTTTT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705877 | ACCACACCCAGCTAA[-/TTTTTTTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 27342 |
| rs201909295 | snp | A/G | 0.000998929 | 0.0223264 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756050 | AATAAGTCTTTTATT[A/G]GAATGATGGCGTCTT | 27342 |
| rs201955066 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687136 | TTTTTTTTTTTTTTT[C/T]TTTTTTTGAGACGGA | 27342 |
| rs201955909 | snp | C/T | 3.30945e-05 | 0.0040677 | missense | RABGEF1 | GRCh38.p7 | 7:66799394 | CAGAAGTGTCTGATA[C/T]GGTGGTGAAGGCGAT | 27342 |
| rs201962985 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720869 | ATTGAATTTCCATAT[A/G]CTAGCTCAAACAATG | 27342 |
| rs201969914 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720192 | TTATTATTATTATTA[A/T]TATTTTTTTTTTTTT | 27342 |
| rs201980062 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746802 | CTAATTTTTTTTTTT[G/T]CTGGAGTGAGACTGA | 27342 |
| rs201990633 | snp | C/T | 0.00535082 | 0.0514469 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797528 | GCTTATTTTGTTTTG[C/T]TTTGTAGTTACTACC | 27342 |
| rs201992340 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743926 | ATGAGCCACTGCACC[C/T]GGCCCTAAAATGGAA | 27342 |
| rs201995935 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738020 | GTGTTTTTTGTTTTT[G/T]TTGTTTTTTTTTTTT | 27342 |
| rs202015022 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772491 | ATGGCATCTAGCTCA[A/G]TGATAAAACACAGTA | 27342 |
| rs202075548 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728819 | CCACCTTCACCTCCA[C/T]CCTCAAGACCACCTT | 27342 |
| rs202099089 | in-del | -/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744385 | AAAAAAAAAAAAAGA[-/C]TAGCCGGGCGCAGTG | 27342 |
| rs202105795 | snp | C/T | 1.70956e-05 | 0.00292361 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808844 | CGACTCGAGTATGCA[C/T]AGCTTTCCTAATATG | 27342 |
| rs202115107 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711406 | ATCTTTTTGTGCTAA[-/T]TTTTTTTTTTTTTTT | 27342 |
| rs202174370 | in-del | -/TTTC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713141 | CTTTTTTTCTTTTCT[-/TTTC]TTTTTTTTTTTTTTT | 27342 |
| rs202182255 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797299 | ACAGAGCCAGACTCT[G/T]TGTTTGCAAAAAAAA | 27342 |
| rs202212367 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683917 | AGCTGATTTTTAAAG[A/C]TTTTGTAAAGATGTT | 27342 |
| rs202225343 | in-del | -/TTTG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796583 | TTGGAAGAAGATTTT[-/TTTG]TTTGTTTGTTTGTTT | 27342 |
| rs207468004 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701756 | TCAGGGATCCACCCA[C/T]CTCAGCCTCATTTAT | 27342 |
| rs367546520 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798164 | CCTCATTCCTCCCAG[G/T]GGTGTGCATTTTTCA | 27342 |
| rs367574940 | snp | C/G | 1.7753e-05 | 0.00297929 | utr-variant-3-prime | RABGEF1 | GRCh38.p7 | 7:66809297 | TGATCACAATTTAGT[C/G]GAGAGTATTTATTTG | 27342 |
| rs367577091 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756251 | TTTTTTTGTTTGCCT[A/G]TCAGATTGACAAAAA | 27342 |
| rs367599914 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725222 | TTACTTTACCATACA[A/G]TTCACTAATTTAACA | 27342 |
| rs367606687 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683861 | ACCTCCCACCTCAAC[A/C]TCCCGAGTAGCTGAG | 27342 |
| rs367614527 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698526 | GAGCCCGGGTCTGGA[C/T]GATGGGTGAGGGGAG | 27342 |
| rs367710628 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695352 | GTCTGAGATGAGATC[C/T]GAGGGCCACTCACAT | 27342 |
| rs367740822 | in-del | -/GA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785879 | ACTCCATCTGGGGGG[-/GA]AAAAAAAAAAGTCTT | 27342 |
| rs367832836 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66682174 | GGAACCCAGACCTGC[C/G]GAGCGACGTGGGCGA | 27342 |
| rs367869124 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743318 | TCGTCTCAAAAAAAA[A/G]AAAAAAATTTAAAAA | 27342 |
| rs367885594 | in-del | -/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696713 | AAAAAAAAAAAAAAA[-/G]AAAAATGGAGCGTGG | 27342 |
| rs367972683 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714652 | TTAAAACAGAAATTT[A/C]GGGCCAGGCGCAGTG | 27342 |
| rs367997746 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780820 | TGGTAATATGGTCCA[C/T]GTTCTTAAGTTTACT | 27342 |
| rs368047167 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798704 | TGTGGTGGCTCGCAC[C/G]TGTAATCCCAGCACT | 27342 |
| rs368054834 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732068 | CAGCCACCCCCAGCC[C/T]AGCCTGCTTCTGCCA | 27342 |
| rs368074307 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794608 | AAGGGCCATAGGGAA[A/G]TAAGTGCATACACGT | 27342 |
| rs368106136 | in-del | -/A/AA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797306 | AGACTCTTTGTTTGC[-/A/AA]AAAAAAAAAAAAAAA | 27342 |
| rs368118792 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681508 | CTATCAAGCGATCCT[C/G]CCACCTCAGCCTCCC | 27342 |
| rs368123587 | snp | C/T | | | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760506 | TGGAGTGCAATGGCA[C/T]GGCCTCACTTCATCA | 27342 |
| rs368151466 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785743 | GCTGGGCGTGGTGGC[A/G]GGCGCCTGTAGTCCC | 27342 |
| rs368160674 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767105 | TCTCCCCGGTTCATG[C/T]GATTCTTGTGTCTCA | 27342 |
| rs368161326 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785668 | TCACAAGGTCAGGAG[A/G]TAGAGACCATCCTGG | 27342 |
| rs368206221 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720654 | AAGGCAAGCATGTCC[A/C]CTCTTGCTGCTTGCA | 27342 |
| rs368216053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703742 | ATTTGAGTCCTCCAA[C/T]TTTGTTCTTTTTCAA | 27342 |
| rs368237496 | snp | C/T | 0.000112886 | 0.00751201 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783862 | TTGAGAATAACCACG[C/T]AGAAACATAGAGTTT | 27342 |
| rs368286166 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704810 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 27342 |
| rs368292430 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684759 | CCTGCTTCAGTCTCC[C/G]GAGTAGCTGGGACTG | 27342 |
| rs368294154 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698926 | TGCTCTTTCCCCTTG[A/G]CTGGTCACAAGTAAC | 27342 |
| rs368301658 | snp | C/G | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754149 | TGGGACTACAGGCGC[C/G]CTCCAACACGCCTGG | 27342 |
| rs368350004 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728900 | TCTCCAAACTCACCT[C/T]CACGCTCACCTGCAT | 27342 |
| rs368365238 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706884 | CCTCCCGGGTTCACG[A/C]CATTCTCCTGCCTCA | 27342 |
| rs368452742 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752493 | AGTGAAACTCCGTCT[-/A]AAAAAAAAAAAAAAA | 27342 |
| rs368485029 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765376 | GCTTTTATTGTATGC[C/T]AAGTAATCCACAGAG | 27342 |
| rs368507245 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806715 | GTGGTGTGATCTCAG[C/T]TCACTGCAACCTCCG | 27342 |
| rs368551532 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697723 | CGGCCTCAGCGAGGT[G/T]GGGGGTGTTCATGTT | 27342 |
| rs368564179 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782095 | TTCACTTTCAAACAC[C/T]AAAGAATTTTTTTCT | 27342 |
| rs368646005 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793340 | AGGTAATTTTATACC[A/C]CATTTTAAGCAGTTT | 27342 |
| rs368705875 | in-del | -/GACCAGACTGGCCA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779317 | AGACCAGACTGGCCA[-/GACCAGACTGGCCA]ACATGGTGAAACCCT | 27342 |
| rs368723024 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789639 | AGTGAGCCTAGATCA[C/T]GCCACTGCACTCCAG | 27342 |
| rs368776157 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785975 | TCTAGATGGTATCCT[A/G]AGGGCCTATGCAATA | 27342 |
| rs368802409 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724422 | TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG | 27342 |
| rs368851321 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747797 | ATGTTTTCTTATTGT[A/G]CTATAATTTTTTTCA | 27342 |
| rs368878920 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807681 | TCCTTTTAGTGGCAA[A/T]GCCATGTCTCCATTC | 27342 |
| rs368883266 | in-del | -/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705707 | AGTGTTTTTTTTTTT[-/G]TTTTTTTTTGTTTTG | 27342 |
| rs368897505 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687504 | AAAAAAAAAAAGAAA[A/G]AAAAAAGAAAAGAAG | 27342 |
| rs368901326 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66685218 | AGAGTGCAGTGGTTT[A/G]ATCTTGGCCACTACA | 27342 |
| rs368910182 | snp | C/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66738988 | GAGGAGTTTCACTCG[C/T]TGCCCAAGCTGGAGT | 27342 |
| rs368967901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746949 | CAGGCACGCGCCACC[A/G]TGCTGAGCTAATTTT | 27342 |
| rs368973774 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774216 | AAGTCTTTTGAATTT[G/T]ACCTTTTGTACTCCT | 27342 |
| rs368975763 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800933 | ATGAATAGTGGGACT[C/T]GATAGGAGAGGCTGC | 27342 |
| rs368983701 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771173 | AGACAGAGTCTTGCT[C/G]TGTCACCCAGCCTGG | 27342 |
| rs368989662 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758201 | ACTACTCACATCTGC[A/C]AAGTATTTTCGTTTT | 27342 |
| rs369011807 | snp | C/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754158 | AGGCGCCCTCCAACA[C/T]GCCTGGCTAATTTTT | 27342 |
| rs369161147 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790731 | AACCAGTAGGTAAAC[A/G]GAAAAGTAAGCTGAT | 27342 |
| rs369167466 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772630 | AATTAAACGATGGGC[C/T]GGGCGCAGTGGCTCA | 27342 |
| rs369169707 | snp | A/G | 1.6473e-05 | 0.00286988 | missense | RABGEF1 | GRCh38.p7 | 7:66805320 | CACGCCTTCAGTCTA[A/G]TATCCAGTATATCAC | 27342 |
| rs369172232 | in-del | -/AGTT | 0.00119784 | 0.0244435 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703429 | AATTTTAGCTCTCAC[-/AGTT]AGGTCTTTTATCCAT | 27342 |
| rs369176840 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733109 | GTGCTCTCTGGTTCC[C/T]TCTCCCTGTGCACCT | 27342 |
| rs369210150 | snp | C/G | | | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756562 | TCATTGTCCTGTTCA[C/G]ATTTTTTTTTCTAGT | 27342 |
| rs369223576 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787412 | GCAGTGGCGTGATTT[C/T]GGCTCACCCCAACCT | 27342 |
| rs369227518 | in-del | -/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687136 | TTTTTTTTTTTTTTT[-/C]TTTTTTTGAGACGGA | 27342 |
| rs369248630 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694587 | AGCCTTTGGCTCCCT[A/G]TGGAGAACCAGCTGG | 27342 |
| rs369270888 | snp | A/G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780099 | ATGTGTGGGAGGGAG[A/G/T]CATGTTGTAAGCAAA | 27342 |
| rs369273619 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799308 | AGCTCTTGTTTACTG[C/T]CTCTCTCTCTTTAGA | 27342 |
| rs369294011 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706665 | ATGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 27342 |
| rs369317930 | in-del | -/TTTTT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720195 | TTATTATTATTATTA[-/TTTTT]TTTTTTTTTTCTTTG | 27342 |
| rs369360195 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730613 | ACCCAGGCTGGAGTG[C/G]CATGGTACAGTCTCG | 27342 |
| rs369412392 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783327 | TGACTAGTTTTATAA[A/G]CTCCAGCAGTCTTTG | 27342 |
| rs369435781 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693391 | CTGGCTTCCTTACTC[C/G]CTGGTTTCCTGGCCT | 27342 |
| rs369520412 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804069 | TTGAACTAAGTGTGT[C/T]GGATTCCAGTAGCTG | 27342 |
| rs369524458 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712752 | TGCTGGGATTATAGG[C/T]GTGAGCCACTGCACC | 27342 |
| rs369579457 | in-del | -/CTCT | 0.0185938 | 0.0946107 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732697 | AGCTGCGCTCTTGTG[-/CTCT]CTCTCTCTCGCTCAC | 27342 |
| rs369588081 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785842 | TTGCACCACTGCACT[C/T]CAGCCTGGATGACAG | 27342 |
| rs369636129 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743020 | GTGTGGTTAAAATGG[G/T]TCTCTCTGGCCAGGC | 27342 |
| rs369648076 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731453 | TGTGCATGATGGCTC[A/G]CACCTGTAATCTCAG | 27342 |
| rs369774402 | snp | A/C | 1.65211e-05 | 0.00287407 | missense | RABGEF1 | GRCh38.p7 | 7:66805140 | TTTTCTGCTTTGTAG[A/C]TATCATTGAAATGGA | 27342 |
| rs369792376 | in-del | -/AGACCAGACTGGCC | 0.0267878 | 0.112589 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779302 | AAGGTCGGGAGTTCG[-/AGACCAGACTGGCC]AGACCAGACTGGCCA | 27342 |
| rs369797306 | in-del | -/AATA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692084 | ACAAACAAACAAATA[-/AATA]AATAAATAAAAGTGT | 27342 |
| rs369842388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777096 | AGTGTTAGCTGTTTT[A/G]AAATGCAAGTTATTC | 27342 |
| rs369848918 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795921 | AAGCAGGCGGATCAC[A/G]TTAGGCCAGGAGTTC | 27342 |
| rs369852308 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | RABGEF1 | GRCh38.p7 | 7:66768877 | ATGTCTTTCCACCAC[C/T]GCCTGCACATTTGAG | 27342 |
| rs369857086 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743724 | GCCAGGATGGTCTCA[A/G]TCTCCTGACCTCGTG | 27342 |
| rs369874058 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795338 | GGCAACAATGGATAT[A/T]GGAAATAATATTAAT | 27342 |
| rs369876916 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717625 | GTGCAGTAGTACAAT[A/C]ACAGCTCACTACAGC | 27342 |
| rs369897560 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682423 | CAGCGCCGCCTGCCC[C/G]GTTTCAGGCCGCCCT | 27342 |
| rs369904172 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701289 | AGATGGCTTGAGCCC[A/G]GGCGCTTGAGACTAG | 27342 |
| rs369936720 | snp | C/T | | | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757416 | TTTATTTTCTTTAGG[C/T]CTTTCAGATACATAG | 27342 |
| rs369955339 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791316 | TTAAGTCTGTATTCT[A/G]CTAGTTACTAATGAC | 27342 |
| rs369968421 | snp | A/T | 0.000153988 | 0.00877328 | missense | RABGEF1 | GRCh38.p7 | 7:66808935 | CCCAGTCTTTGAATC[A/T]AAGTCAGGAGGATTT | 27342 |
| rs369999032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718700 | CCTGAGTATGTACCA[C/T]GCAGTGGCCAGCCTG | 27342 |
| rs370001115 | in-del | -/G | 0.498059 | 0.0310896 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797322 | AAAAAAAAAAAAAAA[-/G]AGAGAGAAAAAATAT | 27342 |
| rs370041692 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787257 | CAAGCTAGTCTTGAA[C/T]TCCTGACCTCAAGTG | 27342 |
| rs370106458 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66809599 | AAATAATTGCCTTTT[A/C]AAGGATTAAACAAAT | 27342 |
| rs370153189 | snp | A/G | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680308 | CTGGAGTGCAATGTC[A/G]TGATCTCGGCTCACT | 27342 |
| rs370153870 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772622 | ATGTTAAAAATTAAA[A/C]GATGGGCCGGGCGCA | 27342 |
| rs370155666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693884 | GAGATCTCGGCTCAC[C/T]GTAACCTCCGCCTCT | 27342 |
| rs370198507 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684967 | ATGGAATCCCTATAT[A/G]TTTCCCAGGGTGGTC | 27342 |
| rs370268047 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707637 | AAGTTGCAGTGAGCC[A/G]AGACTGCACCACTGC | 27342 |
| rs370268570 | snp | C/T | 1.65007e-05 | 0.00287229 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66775344 | GACCCGCAAGGTTAC[C/T]ACAGTGAAGAAATTC | 27342 |
| rs370317967 | snp | A/G | 1.64846e-05 | 0.0028709 | missense | RABGEF1 | GRCh38.p7 | 7:66809094 | AAGAAAGGATCATGA[A/G]TGAAGCCAAGAAACT | 27342 |
| rs370411059 | in-del | -/ACCTTT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729592 | TCCATCCTTACTTCC[-/ACCTTT]ACCTTCACCTTCACA | 27342 |
| rs370432186 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741653 | GAGTTGGTTTTTGGC[C/T]TGGAGAGCTGCTTTC | 27342 |
| rs370445936 | in-del | -/C | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784755 | TGCTTTCTCGCCCTT[-/C]AGAAATGTAATTAGA | 27342 |
| rs370498866 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790910 | ACTCTAGTGACATCA[A/C/G]AGTATTTTAAATGAA | 27342 |
| rs370510240 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788365 | GAGAAGAATCACTTG[A/G]ACCCAAAAGGTGGGG | 27342 |
| rs370556851 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802820 | TGGCAATAGCAGCCA[C/T]ACATCCAGATAAAAC | 27342 |
| rs370597222 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797283 | CACTCCAACCTGGGC[A/G]ACAGAGCCAGACTCT | 27342 |
| rs370604380 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697253 | CTCTCTGCCCCAAGA[A/G]CCTCTACTTCCCCAC | 27342 |
| rs370607071 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713234 | GCAAGCTCTGCTTCC[C/T]GGGTTCATGCCATTC | 27342 |
| rs370658206 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770003 | CTATCGCCAGCATCC[C/G]CAAGTGGTCTCTCTA | 27342 |
| rs370687957 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794264 | AAAATTTTTTAATTT[C/T]TTTCTTTCTCTTTCT | 27342 |
| rs370709024 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738144 | TATCACCTCGGCCTC[C/T]AGAGTAGCTGGGATT | 27342 |
| rs370734660 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691820 | ACACTTTGGGAGACT[A/G]AGGCGGGAGGATCAC | 27342 |
| rs370816788 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690929 | TCTCTACTAAAAATA[A/C]AAAAAAAAAAAATTA | 27342 |
| rs370855813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693250 | GCTGAATGGGTGGCA[A/G]TTGGAGACTTCACAG | 27342 |
| rs370945392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724293 | AAGATTTTTCTCTTT[A/G]TTTTTGGTATTCAGC | 27342 |
| rs370946207 | in-del | -/TCTC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732706 | CTTGTGCTCTCTCTC[-/TCTC]GCTCACTCTCTCTCG | 27342 |
| rs370957584 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733701 | AGGCTCCATCTCAAC[A/C]AAACAAAACAAAACA | 27342 |
| rs371038122 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802013 | CTCACAGGCTCAAGC[C/G]ATCCGTCCGCCTCAG | 27342 |
| rs371039914 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784008 | CTAAAACCCAACTCT[G/T]AGGCTAGTACTTTTC | 27342 |
| rs371070675 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709617 | CATGGTGAAACCCTG[A/T]CTCTACTAAAAATAC | 27342 |
| rs371072745 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728077 | GCCTGGCCCTGCCTC[C/T]GCTCCTCATCACCCC | 27342 |
| rs371077070 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706191 | ATAGACATGAGCCAC[C/T]GTGCCCGGCCTGTTT | 27342 |
| rs371086025 | snp | A/C | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754811 | TGTGTGTATCACTTT[A/C]CCCAGCCACAGCAAG | 27342 |
| rs371128364 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759486 | TTGGTCACATAGTAT[A/G]TTAGTTCGTTCATTC | 27342 |
| rs371196175 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751064 | GACGGAGTCTCTCAC[A/T]TTGTCGCCTAGGCGG | 27342 |
| rs371324730 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738605 | GGTGTGCTGGCACAC[A/G]CCTATCATCCCAGCT | 27342 |
| rs371406858 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793805 | GACCCCAAGTGTCCT[C/G]CCATCCTTTTAGAGT | 27342 |
| rs371414137 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775058 | TGAAATCTGTAGTGC[A/T]TGAAGAGCCGTCCAT | 27342 |
| rs371428913 | in-del | -/GTT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738023 | TTTTTTGTTTTTTTT[-/GTT]TTTTTTTTTTTTTGA | 27342 |
| rs371440792 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689754 | TTGCAGTGAACCGAG[A/G]TTGCACCATTGCACT | 27342 |
| rs371442981 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742639 | AGAGAGAGGGTCTCA[C/T]TTTGTCACCCAGGCT | 27342 |
| rs371459837 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697626 | CCTGCCAGAGTAGGC[A/G]GGATATTCTTGGCCT | 27342 |
| rs371464167 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66753594 | GTTCCAGTTGGGGTA[C/G]GGTAATTTCCCTTTC | 27342 |
| rs371472510 | in-del | -/AG | | | utr-variant-3-prime | RABGEF1 | GRCh38.p7 | 7:66809389 | TGCTTATAAATGWSA[-/AG]GCATTTTTTAAAGGT | 27342 |
| rs371489755 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757650 | GGAGTCTCGCTCTGC[C/T]GCCCAGGCTGGAGTG | 27342 |
| rs371497215 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765691 | GAAGGATCATGTCAC[A/G]CAGCTCCATCATTCA | 27342 |
| rs371506703 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795282 | TTTGTGGCTGTGAGA[C/T]GGACAAGGATCCCGT | 27342 |
| rs371542576 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728716 | TCAACTTTCAGCTCT[A/G]TCCTCACCTCCACCT | 27342 |
| rs371549876 | snp | C/G | 1.65053e-05 | 0.0028727 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66775326 | AAAGAAAACCAACGA[C/G]AAGACCCGCAAGGTT | 27342 |
| rs371555195 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728229 | CTCCTATCCCATCTG[C/T]TGCCTGGGTTCTGCC | 27342 |
| rs371559082 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686417 | TTCCAGGCTGCAGTG[A/T]GCTGTGATCAAGCCA | 27342 |
| rs371564334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804333 | CAAATTGGGACTGTC[A/G]AAAAACATTCTAAAA | 27342 |
| rs371600188 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774931 | TCTGTAGCAGTTGTT[A/T]ACTTACCTTTTTGTC | 27342 |
| rs371622212 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742757 | GACTGCAGATGCGTG[C/T]CACCACACCCAGCTG | 27342 |
| rs371634513 | snp | C/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739699 | TAGACTGAAAAATTA[C/T]GCAACCTGTCCAAGA | 27342 |
| rs371649195 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803612 | GTGAAATTTTTCTGC[C/T]GGGAGCAGTGAGTCA | 27342 |
| rs371673239 | snp | A/G | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754147 | GCTGGGACTACAGGC[A/G]CCCTCCAACACGCCT | 27342 |
| rs371750090 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698801 | TTTGTGTCAGACCCA[C/T]GGGAGTTTCACTCCT | 27342 |
| rs371792472 | in-del | -/A | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760012 | GTACCGTAACCATAC[-/A]AAAACACCCTTATCA | 27342 |
| rs371852139 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735685 | TGTAGCACCTCCCCC[C/T]CTCTCTCTCTTCCCT | 27342 |
| rs371904386 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769213 | TCTGGTCTTCCCCAC[A/T]TCTCCATTTTGCTTT | 27342 |
| rs371927493 | snp | C/T | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681480 | GGGATCTCTGCACCC[C/T]CAACTTCCTGGGCTA | 27342 |
| rs371982698 | in-del | -/CTCT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732733 | GCTCACTCTCTCTCG[-/CTCT]CTCTCTCTTGCTGTC | 27342 |
| rs372012876 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688009 | AGAATCGCTTGAACC[C/T]AGGAGGCAGAGGTTG | 27342 |
| rs372024524 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790928 | TATTTTAAATGAACA[A/G]AATGTCTTTGGGAAT | 27342 |
| rs372031131 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794356 | AGATGGGGTCTCACT[A/G]TGTTGCCCAGGCTGG | 27342 |
| rs372040491 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680440 | GTAGAGACAGGGTTT[C/T]TCTCTGTTGGTTCTG | 27342 |
| rs372048503 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688639 | ACAAATATATGGAAA[A/G]TAAACACACTCTTAA | 27342 |
| rs372079292 | in-del | -/GG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806835 | TTTTAGTAAAGACGG[-/GG]TTTCACCTTGTTGGC | 27342 |
| rs372209070 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808011 | ACTAATAATTGCTAC[C/T]GTGTATTCATTGCTC | 27342 |
| rs372213231 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693726 | TCAGGAGGGTCCCGA[A/G]AGAGAGGACTACGAC | 27342 |
| rs372329768 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709192 | TTTTGTATTTTTAGT[A/T]GAAATGGAGTTTCAC | 27342 |
| rs372337640 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735243 | TTTTTAGGTAGGATT[C/G]GTTCTTATACATAAT | 27342 |
| rs372353610 | in-del | -/TCTA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761224 | TCACTTCCTGCACTA[-/TCTA]CCAGGAGATAGTGTC | 27342 |
| rs372356736 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803863 | CACTGTACTCTAGCC[A/G/T]GGGCAACAGAGTGAG | 27342 |
| rs372392936 | snp | G/T | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760440 | AAAGTTGGTTAGCAT[G/T]TATTTTTTTTTTTTT | 27342 |
| rs372530714 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715033 | TTCCTCCTCTTTCTT[C/G]TTCACTACTTCTTCT | 27342 |
| rs372539877 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764842 | TCCTTGTGCCAGTAC[C/T]GCGCTGTAGTAATTA | 27342 |
| rs372540951 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747187 | ATGATCAATTAATTA[A/C]ATGTGGTTAAAAGTC | 27342 |
| rs372558177 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780417 | ACCTGATAGACTTGT[A/G]AGGATTATACAAAAT | 27342 |
| rs372561350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698994 | AGCTGAGTCCAGCCC[A/G]TCCTTCAGTCCCACA | 27342 |
| rs372633308 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782346 | TCCCACTTTCAGACA[A/G]CTTTTGTTACTAGTT | 27342 |
| rs372639195 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765130 | CACAGGTCCTATGAG[G/T]CTTAGTTGGGTGAAA | 27342 |
| rs372652221 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787503 | TGTGCACCACCATGC[C/T]GAGCTAATTTTTTGT | 27342 |
| rs372663548 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66753768 | CTGGTGTGCAGTGGC[A/G]CGATCTTGGCTCGCT | 27342 |
| rs372704725 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768166 | TTTCAAACCTTTGAT[A/G]TGAAGGGAGACATTA | 27342 |
| rs372754647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750622 | GCTATAAATATATTG[A/G]TACATTTAAATATAA | 27342 |
| rs372762005 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729349 | CCTCTGTTCTCCCTT[C/T]CTCACTTCAATCTTC | 27342 |
| rs372770877 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743421 | CCTCCACCACCCATG[A/C]TTAAGCTATCCTCTT | 27342 |
| rs372773288 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785772 | CCAGCTACTTGGGAG[A/G]CTGAGGCAGGAGAAT | 27342 |
| rs372779331 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767448 | CCAAAAAACTTTCTC[A/G]TGCTAATCCTTTATA | 27342 |
| rs372795506 | snp | A/G/T | 8.23735e-05 | 0.00641723 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795601 | GGGAAAGGTAACACT[A/G/T]TTAGCCATTGAGAGA | 27342 |
| rs372845983 | snp | C/G/T | 0.00398763 | 0.0445073 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689041 | GAGGTTGCAGTGAGC[C/G/T]GAGATTGCACCACTG | 27342 |
| rs372869443 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788460 | AAAAAAAACAAAAAA[A/C]AAAACAAAACAAAAC | 27342 |
| rs372875268 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66685931 | GTGTAAACCTAACAC[C/G]TGTGACTCAGAATAG | 27342 |
| rs372892101 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687511 | AAAAGAAAGAAAAAA[A/G]AAAAGAAGAAGAAGA | 27342 |
| rs372896744 | snp | G/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754151 | GGACTACAGGCGCCC[G/T]CCAACACGCCTGGCT | 27342 |
| rs373051762 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772775 | AAGTTAGCCGGGCAT[A/G]GTGGTACGCATTTGT | 27342 |
| rs373069699 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782838 | TTTCGTTTTGGAAAT[C/T]ATTGGGATATGGGGA | 27342 |
| rs373080496 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796309 | ATACTAGACTTTAGG[A/G]TATACTTAGCACATG | 27342 |
| rs373115125 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769479 | AGTTAGGCTTCCACT[C/G]TGATCAGCAGAGCAT | 27342 |
| rs373116382 | in-del | -/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705487 | AGAGAGAGAGAGAGA[-/G]GAGGGGGGAGGGGGA | 27342 |
| rs373129290 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768389 | TTAAATTGGGTGGTT[G/T]GTTTTCTGACATCTG | 27342 |
| rs373149667 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810346 | TAGAATGTTCAGCAG[C/T]ATTCCTGCCATCCAT | 27342 |
| rs373155119 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792500 | ATGCAGAGAAGACCA[A/G]GGAAAGCCTGTGCAT | 27342 |
| rs373163452 | snp | C/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755667 | GTACAAAGTAGGCTA[C/T]GGTAGCCAGATTATC | 27342 |
| rs373180757 | in-del | -/AGG | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759549 | GTAATTTATAAAGAA[-/AGG]AGGTTTAATTGGCTC | 27342 |
| rs373196335 | snp | A/G | 0.021333 | 0.101051 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682474 | GTGCGCGGCCTCTCC[A/G]TCCAACGTGCTCGTT | 27342 |
| rs373206289 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733166 | CTGGAAAGTCTTGGC[C/T]GTTTGGCAGTGCCCC | 27342 |
| rs373212093 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748310 | CTGATTTAAGGATCT[A/G]TTTTAGATTATCTAG | 27342 |
| rs373227532 | snp | A/G | 8.30461e-05 | 0.0064433 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66771944 | TCATGTGGATCAATC[A/G]GATCTCCTGTGCAAG | 27342 |
| rs373230562 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741157 | CCTTCCGTCCAGGCC[G/T]CTGGCTCCGAAGCAG | 27342 |
| rs373241365 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717770 | TTGCTCTGTTGGCCA[C/G]GCTGGTCTCAAATTC | 27342 |
| rs373244983 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796123 | GCCTGGGCAACAGAT[C/T]GAGACTCTGTCTTCA | 27342 |
| rs373261314 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789725 | ATGTATTTGATAATT[A/G]TGTTGAGTGAGTAAA | 27342 |
| rs373295784 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773927 | CGCCTTGGCCTCCCA[A/G]TGTGCTGGGATTACA | 27342 |
| rs373306481 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718692 | AGATATGTCCTGAGT[A/G]TGTACCACGCAGTGG | 27342 |
| rs373308858 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784047 | CTCAGTGGTGTTTGG[A/G]TCATCTTTGTGTGGA | 27342 |
| rs373315327 | snp | C/T | 4.95119e-05 | 0.00497529 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66775333 | ACCAACGAGAAGACC[C/T]GCAAGGTTACCACAG | 27342 |
| rs373320816 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66809933 | TAGCCTTAACTTTGA[G/T]GTTCTATATAGTCAG | 27342 |
| rs373329517 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795351 | ATTGGAAATAATATT[A/C]ATGGATAGGTTTTAC | 27342 |
| rs373405394 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806368 | TGTAAGTAGGTTCCC[-/A]AAATTGTATAAGCTT | 27342 |
| rs373433854 | in-del | -/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768450 | ATGTAAGTTCTTTGC[-/C]AAATATGTGATTTGC | 27342 |
| rs373450031 | in-del | -/CAAA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762071 | AAAAAAACAAAAAAA[-/CAAA]AACAAAAACATAAAA | 27342 |
| rs373504012 | snp | C/G | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681417 | TTTTTTTTTCTTTTT[C/G]AGACAGGGTCTCGCT | 27342 |
| rs373518093 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691112 | ACAAAAAGAAAATGA[A/C]AACACCAAATGTTGC | 27342 |
| rs373563151 | snp | C/T | 1.67304e-05 | 0.00289222 | missense | RABGEF1 | GRCh38.p7 | 7:66799325 | TCTCTCTCTTTAGAG[C/T]CCTGCGCTGGGTTAC | 27342 |
| rs373609152 | snp | G/T | 1.65803e-05 | 0.00287922 | missense | RABGEF1 | GRCh38.p7 | 7:66799399 | GTGTCTGATATGGTG[G/T]TGAAGGCGATCACAG | 27342 |
| rs373622134 | in-del | -/AC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794233 | TTTTTTTTTTTTTTT[-/AC]TTATTATTGTTAAAA | 27342 |
| rs373626988 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802853 | AATTCACTTTTTACT[C/G]GCTTTCAAAATGTCA | 27342 |
| rs373633306 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66753200 | TCTAAGTGGGTTCAT[A/G]AATAGGATGACCATG | 27342 |
| rs373641984 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722238 | TGAGGTCAAGAGTTC[A/G]AGACCAGCCTGGCCA | 27342 |
| rs373681548 | snp | G/T | 0.000148563 | 0.00861738 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66775364 | TGAAGAAATTCTTCA[G/T]TGCATCTTCCAGGGT | 27342 |
| rs373689339 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775499 | GTCAACTTTTTGAGA[A/T]CATCAGCTCAGATTT | 27342 |
| rs373692116 | in-del | -/A/AA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779670 | AGCGAGACCCTGATT[-/A/AA]AAAAAAAAAAAAAAA | 27342 |
| rs373693473 | snp | A/T | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759875 | GTTCCAAACCATATC[A/T]CATAGGCATATAGTC | 27342 |
| rs373703029 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707687 | AGCAAGACTCCATCT[C/T]AACAACAACAAAAAG | 27342 |
| rs373732862 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708957 | TTCAGTCTTTTTTTT[-/T]CTTTCCTGTTATGCC | 27342 |
| rs373770600 | snp | A/G | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739505 | CTAAAAATACAAAAA[A/G]AAAAATATGAGCTGG | 27342 |
| rs373773014 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791879 | AGCTCTTTAGGAGGC[C/T]GAGGAGGATGGATCA | 27342 |
| rs373789699 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719041 | CCAGCACTCTTGGGG[C/T]CACAGACTCTTGAGA | 27342 |
| rs373790046 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757705 | CAAGCTCCGCCTGCC[A/C]GGTTCATGCCATTCT | 27342 |
| rs373793709 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733614 | GAGGCAGAAGAATTG[C/T]GTGAACCCGGGAGGT | 27342 |
| rs373793969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797994 | TGGTGGCGCACGCCT[A/G]TGATCCCAGCTACTT | 27342 |
| rs373801899 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763306 | GATAGAGAGAGTCTC[C/T]TTCCAGATGCACTCG | 27342 |
| rs373821794 | snp | G/T | 1.64849e-05 | 0.00287092 | missense | RABGEF1 | GRCh38.p7 | 7:66809005 | AGAAGCTGAGAGTTG[G/T]TCTCCTGATGCTTGC | 27342 |
| rs373916017 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691009 | GGCATGAGAATCGCC[A/G]GAACCGGGGAGGCAG | 27342 |
| rs374011194 | in-del | -/A | 0.18325 | 0.240924 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752196 | GACTCTGTCCCAATT[-/A]AAAAAAAAAAGTCTT | 27342 |
| rs374084739 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742983 | GTGACAGAACCAGGG[A/G]AAGTTTTTTAGCTGG | 27342 |
| rs374158835 | snp | A/C | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755294 | GTGAGACTCTGTCTC[A/C]AAAAAAAAACAAAAA | 27342 |
| rs374209580 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771510 | TGTGCTTTTGGTGTC[A/G]TATCCTAGAAGTCAT | 27342 |
| rs374231548 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785460 | TCTGCAAGTTAATGT[A/C]CTTTCAAATAAATAA | 27342 |
| rs374233332 | snp | C/T | 1.67069e-05 | 0.00289019 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66775257 | AGAAGAGGCCTTTGC[C/T]AGCAGTCAGAGCAGC | 27342 |
| rs374275371 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794301 | TCTCTCCTTTCTCTC[C/T]CCTTTCTTTCTTTCC | 27342 |
| rs374289224 | snp | A/G | 4.95757e-05 | 0.00497849 | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66809206 | GCCTCCGAATCAACC[A/G]TTAGCAGCTATTGAC | 27342 |
| rs374315415 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749710 | GGCACGGTGGCTCAC[A/G]CCTGTAATCTCAGCA | 27342 |
| rs374322371 | snp | C/T | 3.33522e-05 | 0.0040835 | intron-variant, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66783697 | GGAAGCAAAAGCTCC[C/T]AGTCCTTCCATAAAC | 27342 |
| rs374341638 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726847 | TGTCTTTACTAAAAA[C/T]ACAAAAATTAGCTGG | 27342 |
| rs374348021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694382 | GGGAGAAGATGGAGC[A/G]AGGATCAGTGAGGCA | 27342 |
| rs374360626 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727903 | TGGCTGCCTCTGGAG[A/C]CTTTTGCCACCATGC | 27342 |
| rs374449570 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713604 | TTATCTTGTACCTTA[A/G]CTTGGGTGAACACAT | 27342 |
| rs374457200 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800004 | GGGAATGAACCAGCA[A/G]GAGTGCAACACAAAC | 27342 |
| rs374526076 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702347 | TGGCTATTGTTTTGT[G/T]TGTGTGTGTGTGTGT | 27342 |
| rs374542176 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794272 | TTAATTTCTTTCTTT[C/T]TCTTTCTTTCCTTTC | 27342 |
| rs374543437 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731978 | TGGGGGAAGGCTGGA[C/T]GATGATCTGGGGAGG | 27342 |
| rs374623210 | snp | C/T | | | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757772 | GCCTGCCACCATGCC[C/T]GGCTAACTTTTTGTA | 27342 |
| rs374663032 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766095 | ATTTGAAACCCAGGA[A/C]TTGGCATACTAAGTA | 27342 |
| rs374708220 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704593 | AGGCGGGTGGATCAC[A/G]AGGTCAGGAGATCGA | 27342 |
| rs374787714 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724987 | GCTCTAGAAGTTCCA[C/T]TGGTTCTCTTTTAAA | 27342 |
| rs374850919 | snp | C/G | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755778 | TGATCTAGTACAATA[C/G]AAGACTGTTGTCTAG | 27342 |
| rs374880758 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768101 | ATTTTGTAAATAGCA[A/G]TTTTTATTTCTCTAG | 27342 |
| rs374906892 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681492 | CCCTCAACTTCCTGG[A/G]CTATCAAGCGATCCT | 27342 |
| rs374972845 | snp | A/T | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760442 | AGTTGGTTAGCATGT[A/T]TTTTTTTTTTTTTTT | 27342 |
| rs375001541 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66753624 | CAGTTTGAAGAGCTC[C/T]CCCTGGTATTTCTTC | 27342 |
| rs375051776 | snp | A/G | | | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756544 | TGAATTTAATAAAAT[A/G]CTTCATTGTCCTGTT | 27342 |
| rs375077101 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706682 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGTGTGA | 27342 |
| rs375080105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684665 | TTTGATACTGAGTCT[C/T]ACTCTGTCAGCCAGG | 27342 |
| rs375096309 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775994 | ATATAACCAGCAAGA[A/G]GATTGTCACTTAAGT | 27342 |
| rs375110748 | in-del | -/G/GT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773083 | CTAGCTAGTTGTTTG[-/G/GT]TTTTTTTTTTTTCAT | 27342 |
| rs375114833 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693286 | TATGTTTCCACCCCC[C/T]AGGGCACCATCAAAA | 27342 |
| rs375135976 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724310 | TTTTGGTATTCAGCA[A/C]CTTGATTGTGATATG | 27342 |
| rs375145906 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779350 | CTCTACTAAAAATAC[A/G]AAAATTAGCTGGGGG | 27342 |
| rs375164902 | snp | C/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754711 | ATATTTATTTGATTG[C/T]GCCATCTAACAAATC | 27342 |
| rs375188546 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752949 | AATTGTTTGAGAAAC[C/T]TAGAAAACATCTATT | 27342 |
| rs375200728 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704926 | TATTTAGTTTTTTAA[A/G]AAACCACCAAACTGT | 27342 |
| rs375226572 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774616 | TTCAGCCTTATTAGT[C/G]AGGTGTGGTGGTGTG | 27342 |
| rs375301261 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759674 | CAAAGTGTCTCCCCT[A/G]GTGGGAGCAGGAGCA | 27342 |
| rs375317842 | snp | A/C | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754155 | TACAGGCGCCCTCCA[A/C]CACGCCTGGCTAATT | 27342 |
| rs375319188 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795769 | GAACTGTACCATGCG[-/T]TATCTTTCCAGGAGC | 27342 |
| rs375331912 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680685 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 27342 |
| rs375351407 | snp | A/G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783050 | ATTGTCTGCCCAGCC[A/G/T]GTGGGATAGTGTAGT | 27342 |
| rs375372939 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808877 | TGTATTAACGTCCTC[C/T]TCTTGTAGTGCTGTG | 27342 |
| rs375411717 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807037 | GAGTCAGACAACCTG[A/G]AAGTCCCTGAGAAGT | 27342 |
| rs375490622 | snp | A/G | | | utr-variant-5-prime | RABGEF1 | GRCh38.p7 | 7:66740695 | GGGGCGGGGCGAGCA[A/G]GAGGGTGGGTGTGAG | 27342 |
| rs375538777 | in-del | -/TAAA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692094 | AAATAAATAAATAAA[-/TAAA]AGTGTATAAATTTGT | 27342 |
| rs375550273 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794766 | AGAAGATAGTCCTTA[C/T]AAAATTATTTATACC | 27342 |
| rs375586083 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714929 | GACAGAGCGAGACTC[C/T]GTCTCAAAAAAACAA | 27342 |
| rs375606440 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807551 | CTCACTGTGCAGTGA[C/T]GGCCTGCAGCTCTGG | 27342 |
| rs375606817 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728816 | CCTCCACCTTCACCT[C/G]CATCCTCAAGACCAC | 27342 |
| rs375611021 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695987 | AAAAATAAAGTGTAG[A/T]TGACTCTTTGAAGCA | 27342 |
| rs375657884 | in-del | -/AA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743327 | AAAAAGAAAAAAATT[-/AA]TAAAAAAAAAAAAAA | 27342 |
| rs375666990 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744904 | TTTCAGTGAAAAAAA[C/T]GTTATCAGCCGCACA | 27342 |
| rs375673945 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749469 | GACCAAAGTTTTGAA[G/T]AGAATATTGTAAGAA | 27342 |
| rs375706641 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750173 | TGTAGATTTTATTTG[C/T]AGTGAGTGCATGTGG | 27342 |
| rs375713088 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727005 | CAAGACTCCATCTCA[A/G]AAAATAATAAAATAA | 27342 |
| rs375744462 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766878 | TACAGGCAAGCGCCA[C/T]CATGCCTGGCTACCC | 27342 |
| rs375751006 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705423 | GCCTGGGCAACAGAG[C/T]GAAACTCCATCTCGA | 27342 |
| rs375752602 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723284 | TCCTACCTTCCTTTA[G/T]ATTGAAGTTTCTTGT | 27342 |
| rs375760534 | snp | C/T | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681410 | TTTTTTTTTTTTTTT[C/T]CTTTTTGAGACAGGG | 27342 |
| rs375792209 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752370 | TATGGTGGCGGGCAC[C/T]TGTAATCCCAGCTAC | 27342 |
| rs375840483 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717609 | TGTCACCCAGGCTGG[A/T]GTGCAGTAGTACAAT | 27342 |
| rs375885047 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722291 | CTAAAAATACAAAAA[C/T]TAGCCAGGCGTGGTG | 27342 |
| rs375889351 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690927 | TGTCTCTACTAAAAA[A/T]ACAAAAAAAAAAAAT | 27342 |
| rs375935909 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691097 | TCCATCTCAAAAAAA[-/A]CAAAAAGAAAATGAC | 27342 |
| rs375986832 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707847 | AGGATTGACCCTTTT[A/G]TCATTCTATAATGTC | 27342 |
| rs375993120 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774456 | AATCAAGATTCCCTA[C/T]CCTCTGGAGCCTTCC | 27342 |
| rs376003232 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776999 | CAATAATACCTACCA[A/G]AGGCACGTGATGAGG | 27342 |
| rs376052385 | in-del | -/AACTT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773369 | TAGTACCTTTATATT[-/AACTT]CTTGTCTGTCCCAGA | 27342 |
| rs376082183 | snp | A/C | 1.64887e-05 | 0.00287125 | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66809029 | TGCTTGCTTAGGCGT[A/C]AAGCAAATGTATAAG | 27342 |
| rs376096738 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712686 | CATGTTACCCAGATT[A/G]GATCTTGAATTCCCA | 27342 |
| rs376136884 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765837 | AGCTGCTGCCAGCTT[A/G]TCTTTGTGGATTGAG | 27342 |
| rs376159962 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748435 | GCTTCCTCACAAGTT[C/G]CTTGAATGCATCTGT | 27342 |
| rs376161692 | snp | C/G/T | 0.000634277 | 0.0177979 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783870 | AACCACGTAGAAACA[C/G/T]AGAGTTTTGGTTTGA | 27342 |
| rs376173944 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701436 | CCCAGGAGGTTGAGG[C/G]TGCAGGGAGCTGTGA | 27342 |
| rs376179617 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733741 | TCCTAGGCCAGGTGC[A/G]CCTATAATCCCAGCA | 27342 |
| rs376192352 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792164 | TACAATGATTAGAGA[A/G]TACTTGAGGTAAAGG | 27342 |
| rs376232108 | snp | C/T | 0.00557542 | 0.0525036 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681871 | TTCCGGCTCCCGATG[C/T]GCAGCAGCGGGAGGG | 27342 |
| rs376283022 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765523 | GGTGTATGACTCAGA[A/G]TCTGAGGATGGGCGT | 27342 |
| rs376302727 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748290 | CGAGTACTTAGATCT[C/G]TAGGCTGATTTAAGG | 27342 |
| rs376313066 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746790 | CACCACGTCCGGCTA[A/T]TTTTTTTTTTTGCTG | 27342 |
| rs376464545 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795972 | GGTGAAACCCCGCCT[C/T]TATTAAAAATACAAA | 27342 |
| rs376490894 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805621 | TACGGAAACAGATGA[C/T]ATGTGTTGGGCATCA | 27342 |
| rs376494424 | snp | C/T | 3.52442e-05 | 0.00419772 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799299 | TATCCTTGGAGCTCT[C/T]GTTTACTGTCTCTCT | 27342 |
| rs376513274 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792226 | TGGAAAATTATGACA[A/G]ACCTTTTGGAGTTTT | 27342 |
| rs376526680 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710428 | TGCTGTCATCTGGTA[C/G]GTATATATTTAATCT | 27342 |
| rs376604357 | snp | C/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754148 | CTGGGACTACAGGCG[C/T]CCTCCAACACGCCTG | 27342 |
| rs376659949 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803621 | TTCTGCCGGGAGCAG[G/T]GAGTCACACCTGTAA | 27342 |
| rs376663861 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742525 | TGTGTCTTGAAGAAT[A/G]ACTAACATTCAGACT | 27342 |
| rs376677557 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774781 | AACCAAAAAAAGGAT[A/C]CTATTTATCCTTTAA | 27342 |
| rs376684519 | snp | C/G/T | 6.62431e-05 | 0.00575481 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66775288 | CAAGGGGCCCAATCC[C/G/T]TCACATTCTCCAAGT | 27342 |
| rs376730434 | snp | A/G | 0.0707826 | 0.174302 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696707 | AAAAAAAAAAAAAAA[A/G]AAAAAGAAAAATGGA | 27342 |
| rs376944660 | snp | C/T | 5.36572e-05 | 0.00517935 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772100 | GGACTTAACTAGGGG[C/T]GGTTGAACAGTGACG | 27342 |
| rs376970862 | snp | C/T | 5.05097e-05 | 0.00502517 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808873 | TGACTGTATTAACGT[C/T]CTCTTCTTGTAGTGC | 27342 |
| rs376991972 | snp | A/G | 3.29989e-05 | 0.00406182 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66775339 | GAGAAGACCCGCAAG[A/G]TTACCACAGTGAAGA | 27342 |
| rs376999646 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686976 | ACAGGCACCCACCAC[C/T]ACGCCTGGCAAATTT | 27342 |
| rs377004228 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774183 | ACTTGACCAAGTTCT[A/G]TTTCTTCCAACTCAG | 27342 |
| rs377004726 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795277 | AAATTTTTGTGGCTG[G/T]GAGACGGACAAGGAT | 27342 |
| rs377024104 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786972 | AATTTAAATTGCTGA[A/G]CCAAATTAATAAAGC | 27342 |
| rs377036415 | snp | G/T | 0.000130703 | 0.00808297 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799461 | TGTTTTCCCCTTAAA[G/T]TTAACATTTTACTGT | 27342 |
| rs377042359 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781642 | TTTCTCTCATCTTGG[A/G]TAGTTTCCTCATACA | 27342 |
| rs377046919 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765030 | TTTTAATGATTAGTC[A/C]ACTTAATTATATCTG | 27342 |
| rs377241627 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709001 | CTGCATCAGTAGTAT[G/T]ACCTTATTTTAATTT | 27342 |
| rs377256104 | snp | A/C | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680536 | GGCGTGAGCCACCGC[A/C]CCCAGCCATACTTTT | 27342 |
| rs377263369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793074 | GGCTGGGGGAGGAGA[A/G]TATGATCCCTTGACA | 27342 |
| rs377282757 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758924 | TTAATGACTTCAAAT[C/G]CATAGGAAGCTGTAA | 27342 |
| rs377309527 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711548 | GTTTTGTCAAAAATC[G/T]GTTGGCTGTATTTCT | 27342 |
| rs377326593 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766324 | AAAAAAAAAAAGGAA[C/G]CTTAGTGCTTAGTGA | 27342 |
| rs377351480 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723184 | ATGTTGGCCAGTCTG[G/T]TCTCCAATTCTTGAC | 27342 |
| rs377363456 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691799 | TGGCTCACACCTGTA[A/G]TCCCAACACTTTGGG | 27342 |
| rs377381117 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738241 | CCAGGCTGGTCTCAA[A/G]CTCCTGACCTCAGGT | 27342 |
| rs377387098 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794240 | TTTTTTTTACTTATT[A/T]TTGTTAAAAAAATTT | 27342 |
| rs377426806 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693861 | CACCCAGGCTGGAGT[A/G]CAGTGGCGAGATCTC | 27342 |
| rs377450928 | in-del | -/T | | | intron-variant, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66685497 | CATCTCTACAAAAAA[-/T]AAAGAAAAGATTCTT | 27342 |
| rs377452986 | in-del | -/TTCTC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772223 | TGTTTTCCTCTCTTC[-/TTCTC]AGTCAGCTTTTAATG | 27342 |
| rs377456268 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707784 | TTCATGTACTTTGAG[A/G]CTCTGTTTTTCGGTG | 27342 |
| rs377470730 | in-del | -/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690100 | CATTGATAAAAAATT[-/C]TTTTTTTTTTTTTTT | 27342 |
| rs377551994 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807187 | TGCCCTTGGCCTGCA[A/G]CCTTAAGTACATTTG | 27342 |
| rs377564134 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737353 | TTAATCTCCTGGCTC[A/G]AGTAGTCTTCTCCCC | 27342 |
| rs377592917 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741617 | AAATTTTCCCAGGAC[C/G]AGTTTACCGGAGCAC | 27342 |
| rs377595658 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810907 | TTAAGCTTGACACAT[C/G]TGTGTCATCACGCAC | 27342 |
| rs377597141 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792593 | GTCTACCCTTTTCTC[C/T]TGAAGGAGGCACTAT | 27342 |
| rs377632592 | in-del | -/TTATTTAT/TTATTTATTTAT | 0.263323 | 0.270861 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683727 | ACTACAAGGAGGTGC[-/TTATTTAT/TTATTTATTTAT]TTATTTATTTATTTA | 27342 |
| rs377641774 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711762 | CGGCTAATTTTTTGT[A/G]TTTTTAGTAGAGACG | 27342 |
| rs377665275 | in-del | AA/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699698 | TTCCATCTCAAAAAA[AA/C]AAAACAAAACTGGTG | 27342 |
| rs377678390 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733700 | GAGGCTCCATCTCAA[A/C]AAAACAAAACAAAAC | 27342 |
| rs377687900 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794278 | TCTTTCTTTCTCTTT[C/T]TTTCCTTTCTCTCCT | 27342 |
| rs386714082 | multinucleotide-polymorphism | AT/TA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765984 | TAATTGATCTATACT[AT/TA]AAAATAGGTATCTTC | 27342 |
| rs386714083 | in-del | CC/TCT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808233 | CTTTTTTTTTTTTTT[CC/TCT]TGAGACAGTCTTGCT | 27342 |
| rs397701325 | in-del | -/A | 0.5 | 0 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746801 | CAGTCTCACTCCAGC[-/A]AAAAAAAAAAATTAG | 27342 |
| rs397708611 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718574 | ATTTATAAAAAAAAA[-/A]ATAGGCAATGGATTT | 27342 |
| rs397717016 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690941 | ACCACACTCGGCTAA[-/T]TTTTTTTTTTTTGTA | 27342 |
| rs397717888 | in-del | -/G | 0 | 0 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682713 | CCGGCCGCGGCAGGG[-/G]CGCCGGGATTTGATC | 27342 |
| rs397754643 | in-del | -/T | 0 | 0 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718575 | CAAATCCATTGCCTA[-/T]TTTTTTTTTTATAAA | 27342 |
| rs397755147 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733699 | GAGGCTCCATCTCAA[-/A]CAAAACAAAACAAAA | 27342 |
| rs397773173 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746800 | GCTAATTTTTTTTTT[-/T]TGCTGGAGTGAGACT | 27342 |
| rs397841220 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811156 | GTTACTGTACACTCT[-/T]GTTTGTTCAATAAAC | 27342 |
| rs397841507 | in-del | -/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798361 | GAGGTGTTTTAAGGG[-/G]AGAAGGGACTCGGAG | 27342 |
| rs397888969 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724378 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAATAA | 27342 |
| rs397889262 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720522 | TATTTAGTTTGCTGA[-/T]TTTTTTTTTTTTTTA | 27342 |
| rs397889581 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720522 | TATTTAGTTTGCTGA[-/T]TTTTTTTTTTTTTAA | 27342 |
| rs397890414 | in-del | -/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66738749 | CAGAATGAGTGTTTC[-/T]TTTTTTTTTTTTTTT | 27342 |
| rs397890515 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695976 | GTCATCTACACTTTA[-/T]TTTTTTTTTTTTGAG | 27342 |
| rs397956680 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772456 | ATTATTTCCCTCATT[-/T]CTTTTAATATATATT | 27342 |
| rs397966748 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805926 | TTTTTTTTTTTTTTT[-/T]GAGAGATGGGGTCTC | 27342 |
| rs398005003 | in-del | -/A | 0 | 0 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681410 | CCCTGTCTCAAAAAG[-/A]AAAAAAAAAAAAAAA | 27342 |
| rs398005004 | in-del | -/C | 0 | 0 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681595 | GCCACAGAGGGAGAG[-/C]CCCCATCTCTACAAA | 27342 |
| rs398005005 | in-del | -/T | 0 | 0 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688105 | GTCATTTGGTTACTT[-/T]TTTTTTTTTTTTTTT | 27342 |
| rs398095141 | in-del | -/TT | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680551 | CCCAGCCATACTTTT[-/TT]GTTTTATACTCTGTT | 27342 |
| rs527270997 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780265 | TTGTTAATAGTCAAC[A/T]GCTCAGGCTTTGGAT | 27342 |
| rs527274295 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713374 | ACCTCGTGATCGGCC[C/T]GCCTTGGCCCTCCAA | 27342 |
| rs527287560 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801678 | ACTTAACATAATATC[C/T]TCCTGTTTCATCCAT | 27342 |
| rs527302645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794533 | AAGTGAGAAACAAAT[A/G]CATATATTACACCTA | 27342 |
| rs527312652 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713153 | TCTTTTCTTTTTTTT[A/T]TTTTTTGAGACGTAG | 27342 |
| rs527320024 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748439 | CCTCACAAGTTCCTT[C/G]AATGCATCTGTTTTC | 27342 |
| rs527327029 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807389 | TCTGCAACTTCTGTT[A/G]TTCCTTGGCTTCCAC | 27342 |
| rs527371092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683269 | AGACGTGAGCCATTG[C/T]GCGGCTTTAACTGCT | 27342 |
| rs527391472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760901 | CCCAAAGTGCTGGGA[C/T]TGTAGGCGTGAACCA | 27342 |
| rs527415502 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800950 | ATAGGAGAGGCTGCC[C/G]GTTAAGTTACACAGT | 27342 |
| rs527422513 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682746 | GCGTCGCCCTGGGGG[C/G]ACAGAAGCGTCCCGG | 27342 |
| rs527444150 | snp | A/G | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739197 | TCAGGTGATCTGCCC[A/G]CCTCGGCTTCCCAAA | 27342 |
| rs527450969 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725977 | AAAACCCCCATTCAT[A/C]AGGCCTCCCTTGATC | 27342 |
| rs527505603 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688496 | GACATTGTCCAGAGT[A/T]TATAGTGTATTAGGC | 27342 |
| rs527527113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732151 | CACCGCCCTCTCTTC[C/T]TATGGTCCAGGCACA | 27342 |
| rs527542485 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736946 | TACAGACACACACAC[A/G]TACACACACACGCAC | 27342 |
| rs527543752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694700 | GTAGGGAGAGAATGA[A/G]GTCGGAATCTCGTGG | 27342 |
| rs527551443 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737771 | CCTGAGGTGGGAGGA[C/T]TGGTTGAGCCTAGGA | 27342 |
| rs527561185 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731529 | TGAGACCAGCCTGGG[A/C]AACATGGTGAAACCC | 27342 |
| rs527564238 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767005 | TGTCAAGTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 27342 |
| rs527631832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780984 | TTGTTTTTTTAACCT[A/G]ATCTGATAATCTCTG | 27342 |
| rs527632084 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694424 | GATGAACCCGGGGAG[C/T]TGGACGGAACATAAG | 27342 |
| rs527640805 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727893 | AACACACGCGTGGCT[A/G]CCTCTGGAGCCTTTT | 27342 |
| rs527642890 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732446 | CTGGCAGTAAGTGGG[C/T]GTTTTAGGGGAGACT | 27342 |
| rs527654844 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769713 | TCTCAAGTTTTATGT[C/T]TTAAGATAGAGATCT | 27342 |
| rs527657443 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762504 | CTGAGACGAGAGGGT[C/T]GCTTGAGCCTGGGGA | 27342 |
| rs527672999 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802519 | CTCTGAAGAGTAAAT[C/G]ATAGCAGGCAGGCTG | 27342 |
| rs527689801 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791505 | AAAAAAATATGGACA[C/T]GAAAGCTAATACCTA | 27342 |
| rs527693692 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66809878 | AGAAGTGTTTAGACA[A/C]ACTCCCCTTAAGATG | 27342 |
| rs527726022 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727669 | CCGGCCCATGCTCCC[A/C]GCCAGGCTTCTCCAG | 27342 |
| rs527734014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66753659 | GGATGTCTTCGCATA[A/G]CAGTGTTTTTTCTCT | 27342 |
| rs527741045 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690122 | TTTTTTTTTTTTTGA[A/G]ACGGAGTCTCGCTGT | 27342 |
| rs527748271 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751966 | CTTTGGGAAGCCAAG[G/T]TGGGAGGCTCACTTG | 27342 |
| rs527768370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768746 | CCTAGGGGTAAGCCT[A/G]GAAATTGCTTTCTTG | 27342 |
| rs527795870 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796005 | GTAGCCGGGTGTTGT[G/T]GTGCACCTCTTATCC | 27342 |
| rs527809016 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773905 | TCCTGAGCTCAAGTG[A/G]TCCGGCCGCCTTGGC | 27342 |
| rs527832708 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689946 | AAAGGAAAATTAATG[C/G]CAGTTTTTTGCAAAC | 27342 |
| rs527835301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695929 | TGAGATCGCACCACC[A/G]TACTTCAGCGTGGGT | 27342 |
| rs527837758 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782708 | GGAGAATCGCTTGAA[C/T]CTGGGAGGTGGAGGT | 27342 |
| rs527837864 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775107 | CTCAGACTGATTTGG[C/G]ATATTTAGTCTCTAG | 27342 |
| rs527898838 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782202 | GTTTTAAATTAGATT[G/T]TACCTGATTTATTTA | 27342 |
| rs527926306 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687889 | TCGGGAGTTCAAGAC[A/C]AGCCTGACCAACATG | 27342 |
| rs527932412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743928 | GAGCCACTGCACCCG[A/G]CCCTAAAATGGAATT | 27342 |
| rs527935586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738555 | GGCGACATGGCAAAA[C/T]CTTGTCTCTACAAAA | 27342 |
| rs527951829 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701004 | CAGCCCAAGGAAGCC[A/G/T]TCCTGGAGGAGGGAG | 27342 |
| rs527956417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734100 | TGGTCTAACGGGGCC[C/T]TGGGGACACATTCAT | 27342 |
| rs527997181 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749021 | AGGCCTTCAGGCTCA[C/T]CGTGACTTCCTCCAC | 27342 |
| rs528002596 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791719 | AAGTGTATAGAGTGC[-/CT]CTCAGCATAATGTTC | 27342 |
| rs528031553 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785026 | TATTAAGTTAGTGTA[G/T]GTATACTGTAGTACA | 27342 |
| rs528043659 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734797 | ATTTCTCGGTCTTCA[A/G]AAATGACGGACACTG | 27342 |
| rs528059509 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-5-prime | RABGEF1 | GRCh38.p7 | 7:66740714 | GGTGGGTGTGAGGCG[A/G]GAGCTGGCCGCGGAG | 27342 |
| rs528061486 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777560 | CTGTGTCCCAAAAGC[C/G]TCTGTACAGTGTGCA | 27342 |
| rs528065347 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697089 | TCTTCCCTCTGTGTC[A/C]ACCAGGAAGCACAGT | 27342 |
| rs528135374 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740094 | CCACCTCAGCCTCCC[C/T]GGTAGTTGGGACCAC | 27342 |
| rs528136233 | snp | A/C | 0.00517822 | 0.0506191 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740502 | GGTTTCTCCGGGGCT[A/C]CCCAGCGCCCCACCT | 27342 |
| rs528140710 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703178 | AAATGGGGTTTCACC[A/G]TGTTACAGAATGGTC | 27342 |
| rs528149128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745008 | CCATCCTGGCTAACA[C/T]GGTAAAACCCCATCT | 27342 |
| rs528151821 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765159 | AAAGGTGGAGAATGA[C/T]AGGAGCAGAGAGGTT | 27342 |
| rs528159182 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684639 | TGGCTAAATTTTTTG[-/T]TTTGTTTGTTTTTGA | 27342 |
| rs528171564 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784327 | TATGGAGTTTCAGTC[C/T]CTTTATTTTATAGAT | 27342 |
| rs528175226 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709071 | CGCCCAGGCTAGAGC[G/T]CAATGGCACAATCTC | 27342 |
| rs528181446 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761251 | TAGTGTCAGATCACA[A/C]AGGGTGAGGACTCAG | 27342 |
| rs528196265 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744390 | AAAAAAAAAGATAGC[C/T]GGGCGCAGTGGCTCA | 27342 |
| rs528218316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751248 | GTTAGCCAGGCTGGT[C/T]TCGATCTCCTGACCT | 27342 |
| rs528260826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708578 | ACAGGCGTGAGCCAC[C/T]GCCCCTGGCCAGCCC | 27342 |
| rs528291762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796228 | TTGGTGAGTTATTGT[A/G]TTAATAGTTTAAAAA | 27342 |
| rs528387732 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714446 | TGATAATTTATGTCT[C/T]GTTTCCTTTCTTTTC | 27342 |
| rs528394353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763218 | GGTTCAAGCAGGCTC[C/T]GCTGGGTATTCTGCT | 27342 |
| rs528402269 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803154 | CAATAAAACAGCAAA[A/C]ATTATGTAATTCACA | 27342 |
| rs528445076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792207 | CTCTACTATCTTTTT[C/T]TCTTGGAAAATTATG | 27342 |
| rs528487296 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710693 | TTTGGAGAAATGTCT[C/G]TTTAATTTTCCTCCT | 27342 |
| rs528498051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791433 | AAAGAGGATTAAAGC[C/T]CTCATATGGTTCTTT | 27342 |
| rs528502580 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752459 | AGATCATGCCACTGC[A/G]CTCCAGCCTGGGGAA | 27342 |
| rs528507211 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716877 | TCTGTCTCCCAGGCT[C/T]AAGTGATCCTTGTGC | 27342 |
| rs528514873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798649 | CGTGGCCTCCTATAC[A/G]AGCTCCAGTGTGCCT | 27342 |
| rs528521213 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709784 | CCATGTCAAAGAAAA[G/T]AAAAAAGAAAGAAAG | 27342 |
| rs528533638 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693733 | GGTCCCGAGAGAGAG[G/T]ACTACGACCCTCAGG | 27342 |
| rs528573192 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758995 | TAATGGTTACATGTT[A/T]CATAACTATAATGTA | 27342 |
| rs528586907 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765195 | GGGATATAGGAAAGG[G/T]AGTTTCAGAAATATT | 27342 |
| rs528593284 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723546 | CACAATACACTGCTA[A/T]TTTTTCTTTAAACAA | 27342 |
| rs528595479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758454 | GTGCATTCTTTATGC[C/T]CAGGTTGCTCAACCA | 27342 |
| rs528604084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716467 | TTAGCTAGGTGTGGC[A/G]GCATGTGCCTGTAGT | 27342 |
| rs528629765 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805571 | CCATACAGACACTCC[A/G]CCTCCCAGCACTTGA | 27342 |
| rs528629828 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798180 | GGTGTGCATTTTTCA[C/G]CATTCCCTAGTCACA | 27342 |
| rs528655497 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762450 | ACAAAACTTAGCCAG[C/G]CATGGTGCCACATGC | 27342 |
| rs528691580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804759 | AAAAAAAAAAAAAGT[A/G]TGGGCTTTACAGTCA | 27342 |
| rs528701172 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729314 | TCCCCTCCATTCTTC[A/G]TTCCTCATCTCCATC | 27342 |
| rs528708751 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743183 | TGTGATGGCGCCTGC[C/T]GTAATGCTAGCTACT | 27342 |
| rs528731719 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735365 | TGGAAGACTTTATAG[A/C]ATAGTAGTTTAGATT | 27342 |
| rs528749441 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811255 | ATTTTTTTGGAGGTA[C/T]CTCATATTGGTCGAA | 27342 |
| rs528772103 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764026 | TTCTATGGTAATATT[A/G]TTTAATCATTTGAGA | 27342 |
| rs528819943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692102 | AAATAAATAAAAGTG[C/T]ATAAATTTGTTTCAT | 27342 |
| rs528831542 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697547 | CTCGAACACATCCCA[A/G]GTGAGCACTTGGCAG | 27342 |
| rs528838118 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740049 | AGGGATCTCTGCACC[C/G]TCAACTTCCTGGGCT | 27342 |
| rs528911363 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744064 | TTTTTTTAAGACGGA[G/T]TCTTGATCTGTGACT | 27342 |
| rs528912470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789873 | TGTTGGCATTGTCTC[C/G]CAGCCTTCTCAGTTC | 27342 |
| rs528936473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750656 | ACACACATATAATGG[C/T]GCTTGAGAAATAAGT | 27342 |
| rs528952843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708522 | TCGAACTCCTGACCT[C/T]AAGTGATCCGTCCAC | 27342 |
| rs528966789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714894 | GAGCCAAGATCCTGC[C/T]ACTGCACTCCAGCCT | 27342 |
| rs528996653 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749798 | AACACAGTTAAACCC[C/T]GTCTCTACTAAAAAT | 27342 |
| rs529014319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756724 | TCTTTAGAACTTTCA[C/T]GAATACTTCATTTTA | 27342 |
| rs529020297 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706269 | TATTATAAATAAAAC[C/T]GATATGAACATTTTT | 27342 |
| rs529067463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795769 | TGAACTGTACCATGC[A/G]TATCTTTCCAGGAGC | 27342 |
| rs529090154 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720593 | AAACTTAAAGCTAAT[A/T]TTTTAATGGATAAAG | 27342 |
| rs529116200 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66809765 | TGGTGTCTGCTGTGC[A/G]TGGCATTTTATATGT | 27342 |
| rs529129723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756165 | CAAAATCAGTTATTC[A/G]AAGAAAATATACTAG | 27342 |
| rs529130996 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800855 | GCGAGTGTTTGTGTG[A/T]CCCATCAGTGGTGAA | 27342 |
| rs529142470 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776234 | CCAGTTCCTACCCTG[A/G]GGTAATTGTAATGAG | 27342 |
| rs529189977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768701 | TGGAAGCCTTTGGTA[C/T]GGAATAGCGTCAGAT | 27342 |
| rs529192597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762466 | CATGGTGCCACATGC[C/T]ATAGTCCCAGCTACT | 27342 |
| rs529205244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683452 | TATTTAATGACCTTT[C/T]CAATCAGTCAGTTTC | 27342 |
| rs529210037 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727584 | ATGTTTGGTTCTCTG[A/G]GCAGGAAGGGTCAGG | 27342 |
| rs529214307 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761737 | AGGCTGCCCATGAAG[C/G]CTAACACACCCAGCC | 27342 |
| rs529276733 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680810 | AAATTAGCCGGGTGC[A/G]GAGGCTCACACCTGT | 27342 |
| rs529287252 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794835 | TGCACAGTGGTAGAG[G/T]AGAGTCGAAGAAGTC | 27342 |
| rs529303188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751543 | CTAGGCAGGTAGAGT[A/G]GGGCTGATCACCTAA | 27342 |
| rs529310752 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804671 | ACCCAGGAGGCGGAG[C/G]TTGCAGTGAGCAGAG | 27342 |
| rs529338223 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715681 | TCGTTTATATAATTT[G/T]AAATTACAAACAGTT | 27342 |
| rs529345274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757863 | TGATCCGCCCGCCTC[A/G]ACCTCCCAAAGTGCT | 27342 |
| rs529345365 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764605 | TACATTTAGGTCTTT[C/G]ATTGATTCTGAGTTA | 27342 |
| rs529374832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803866 | TGTACTCTAGCCGGG[A/G]CAACAGAGTGAGATG | 27342 |
| rs529447264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728433 | GACCTGGGTCAAGAA[C/T]TATTCTCAGGAAGTT | 27342 |
| rs529473436 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789452 | CTTTGGGAGGCTGAG[A/G]TGGGCGGATCACAAG | 27342 |
| rs529480396 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684795 | ACCCGCCACCATGCC[A/T]GGCTAATTTTTTGTA | 27342 |
| rs529493050 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758017 | GGAAAAAAATCACCC[-/G]TAAGTTTTATTTCTT | 27342 |
| rs529506926 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727995 | TCCTGACAGCTCTCC[A/G]CAGGCCAAACCACTA | 27342 |
| rs529511347 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740473 | AGGGACTGAGCGACA[A/G]ACTAGGAAACGCCGG | 27342 |
| rs529531334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692036 | CACTCCAGCTTGAGC[A/G]ACAAAGCAAGACCCT | 27342 |
| rs529540346 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727641 | CCACAGCCTGTGCAG[C/T]GAGTCGGGAAGGCCG | 27342 |
| rs529550567 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759075 | ATGCACATTTCATCT[-/C]ATACGTAGATTCCTG | 27342 |
| rs529552858 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766108 | GACTTGGCATACTAA[G/T]TATAGGCTTACTTGA | 27342 |
| rs529570587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691303 | ATTAAAAATATACAT[C/T]TACACAAAGACTTGA | 27342 |
| rs529578318 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777379 | GTCTCCTAATTCCTG[A/G]GTCAATATTTTTCCA | 27342 |
| rs529588223 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806933 | ACAGGCATGAGCCAC[C/T]GCACCTGGCCTCATA | 27342 |
| rs529603258 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764695 | CTATCCAATTTTCCC[A/G]GCACTATTTGGTGAA | 27342 |
| rs529606479 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776390 | ACCAAAAACACACCT[C/G]TCTTTAAGACATGGA | 27342 |
| rs529616298 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730564 | TTCTTTTTCTTTTTT[C/T]TTTTTTTTTTTGGTG | 27342 |
| rs529630091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773038 | AAACTGCTTCAACAG[A/G]AGAAAGTCAAATGGA | 27342 |
| rs529649444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723800 | GGTCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 27342 |
| rs529653799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784279 | TAGAGAAAGGACAGA[C/T]AGAATTTAGACAATG | 27342 |
| rs529665846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765519 | CCAGGGTGTATGACT[C/T]AGAATCTGAGGATGG | 27342 |
| rs529683203 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704140 | TATCCCCATCTGGCA[C/T]TAGCAAGCCACACTG | 27342 |
| rs529695995 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781158 | ATCTTTATCTCCACT[A/G]TCAGCTTGTTAGCTA | 27342 |
| rs529782210 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772480 | ATATATTTAGCATGG[A/C]ATCTAGCTCAGTGAT | 27342 |
| rs529786076 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779039 | AGAATCGCTTGAACC[C/T]GGGGAGTGGAGGTTG | 27342 |
| rs529792044 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785702 | TCACGGTGAAACCTT[G/T]TCTCTACTAAAAATA | 27342 |
| rs529798085 | snp | C/G | 0.0501905 | 0.150254 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778280 | CATACGTAGCAGCTT[C/G]GTAGCAGACAAAATA | 27342 |
| rs529810968 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686386 | CCAAAGTGGGAGGAT[C/T]GCTTGAGTCCGGAAG | 27342 |
| rs529821104 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747782 | TATTAATCGAAGAAA[A/C]TGTTTTCTTATTGTG | 27342 |
| rs529855006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785145 | TACTCTGTAATAATT[C/T]AGTAGACTTCTAAAT | 27342 |
| rs529868042 | in-del | -/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737442 | AATACGAGACTGGGT[-/G]AGGGGGGGGCAGTCT | 27342 |
| rs529871790 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693834 | TTTTTTTGAGACAGG[G/T]TCTCACTCTGTCACC | 27342 |
| rs529885257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697650 | TTGGCCTCACCATTC[A/G]CTGAGGATTAGCAGG | 27342 |
| rs529890371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746154 | ATATTATTTAACTTA[C/T]GTTTATCTCTTTGAT | 27342 |
| rs529892410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716859 | TCTCGGTTCACCACA[A/G]GCTCTGTCTCCCAGG | 27342 |
| rs529896010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741070 | TCCAGCGCCAGCCGA[A/G]CCCCGACGGCCTGAC | 27342 |
| rs529905474 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761503 | GGGAAGGTGCAGAAC[G/T]TCCATGCCTTCCCTG | 27342 |
| rs529960571 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66740807 | GGTACGGAGCGGACG[A/G]ACTGGGGCTGAGAGC | 27342 |
| rs530023567 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752047 | ACAAACCAAAAAAAA[A/C]CCGCAAAAAACTAGC | 27342 |
| rs530028904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709673 | CCACCTACTCAGGAG[C/T]CTGAGGCAGGAGAAT | 27342 |
| rs530032230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791225 | TCTTAACGGTTCCCA[C/T]CACCTTTATTTTGCC | 27342 |
| rs530111445 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706328 | TCATTTCTCTTATGC[A/G]ATACCTAGGAATGAA | 27342 |
| rs530131472 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66753087 | AAAAAGCTACAGGAA[C/T]GGGAGAGAGAATTAC | 27342 |
| rs530133059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787133 | CCAGGTTCCAGTGAT[C/T]GTCCTCCCTCAGCCT | 27342 |
| rs530141609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712242 | ATGCCTCTTCATTTA[C/T]TTAGGTCTTTCTAGA | 27342 |
| rs530164531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793536 | TAATCACAAGAATGA[A/G]TATAGTTTCTTCTAA | 27342 |
| rs530182977 | in-del | -/A | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755489 | TCAAGAAAAGAAAAG[-/A]AAAAAAAAGCGTAAA | 27342 |
| rs530222307 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705670 | TTATGTTACTTCAAG[A/C]ACTTTCAGTTTGATA | 27342 |
| rs530227398 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711661 | GCACAATCTCGGCTC[G/T]CTGCAAGCTCCGCCT | 27342 |
| rs530267005 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692336 | CTCCCTCTCTTACCC[A/G]TGCTTCCTGGCATCT | 27342 |
| rs530295955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806538 | GCTTTTACCTTTATT[C/T]ACACTGTTTTCCATC | 27342 |
| rs530319293 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799525 | GTCGAAGGTACATTG[G/T]AATGTAGTAAAAGTG | 27342 |
| rs530346971 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717019 | CCTGGCCTCAGGTGA[G/T]CCGCCCGCCTCAGCC | 27342 |
| rs530359328 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686946 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGAGTA | 27342 |
| rs530390695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778864 | CTCAGGCCTATAATC[C/T]CAGCACTTTGGGAGA | 27342 |
| rs530487063 | snp | A/C/G | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729432 | CATCTCTGTCCTCCC[A/C/G]TCTATTCTCCTCTCC | 27342 |
| rs530506153 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692714 | AGCTCCCACCCACCC[C/T]TCTCTGCAGCCAAGC | 27342 |
| rs530524300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703884 | AGATCATTTTGATGG[A/G]TATTGCCATCTTAAC | 27342 |
| rs530529691 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735445 | TTAATAAATGTGTGA[A/C]CTTGGGTGAGTTACC | 27342 |
| rs530580573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791125 | ATGAAGAACATATGC[A/G]TTCCTTAGACACTGT | 27342 |
| rs530581826 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784446 | ACACCTGTTTCTTTT[A/C]CCCATAATTTCAGTG | 27342 |
| rs530585304 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-5-prime | RABGEF1 | GRCh38.p7 | 7:66740729 | GGAGCTGGCCGCGGA[A/G]CCCAGACCTACCCGG | 27342 |
| rs530629120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737486 | GAGTACCTTTAGATC[C/T]GGATTTCGGGGCTCA | 27342 |
| rs530642502 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790711 | GGCTGTTGGAAAGCA[A/G]AAGTAACCAGTAGGT | 27342 |
| rs530656180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752018 | CCTGGGCAACAAAGA[C/T]CCCATCTATATAAAC | 27342 |
| rs530733474 | snp | C/T | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680852 | TTTGGAAGGCCAAGG[C/T]GGGCGGATCACTTGA | 27342 |
| rs530749432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797053 | ACCTATAAACCTAGT[A/G]CTTTGGGAGGCTGAG | 27342 |
| rs530762780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709167 | GCACCCACCACCATG[C/T]CCGGCTAATTTTTGT | 27342 |
| rs530765535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745065 | GGCATGGTTGCAGGC[A/G]CCTGTAGTCTCAGTT | 27342 |
| rs530791061 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741886 | CTCACGTCTGTAATC[C/T]CAGCATTTGGAAGGC | 27342 |
| rs530802851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705495 | AGAGAGAGGAGGGGG[A/G]AGGGGGAGGAAGCAG | 27342 |
| rs530851524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747089 | GTGAGCTACCGTGCC[C/T]GGCCCTAGTGGAACA | 27342 |
| rs530851858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757756 | AGCTGGGACTACAGG[C/T]GCCTGCCACCATGCC | 27342 |
| rs530869436 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746427 | TCTGCCTCAGCCTCC[C/G]GAGTAGTTAACCACC | 27342 |
| rs530871294 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687244 | GTCCTCCTGCCTCGG[-/C]CCCCCCAGTAGGTGG | 27342 |
| rs530922577 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759625 | TAGGGTGGCCTCAGG[A/C]AGCTTCCAGTAATAG | 27342 |
| rs530960716 | in-del | -/CT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697460 | CTCCCTTCACAGTGG[-/CT]CTCTGTCTGCCCATC | 27342 |
| rs530979565 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702823 | TATTTTCATTGGGTT[C/G]TTTGTCTTTTTGTTG | 27342 |
| rs531044062 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710856 | CTGTAATCGCACCAT[G/T]TTGGGAGGCCAAGAC | 27342 |
| rs531046393 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695839 | GGTGTGGTAGCGAAC[A/G]CCTGTAATTTCAGCT | 27342 |
| rs531047264 | snp | A/G | 0.187685 | 0.242109 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723706 | CTGCCTCAGCCTCCT[A/G]AGTAGCTGGGATTAC | 27342 |
| rs531053896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752566 | CATATTCAGAAAAGG[A/G]AGTCTCCCATTGGGA | 27342 |
| rs531055029 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791431 | TTAAAGAGGATTAAA[C/G]CCCTCATATGGTTCT | 27342 |
| rs531096271 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699890 | GGGAATGATAGCAAA[C/T]CCAGGGCCATTGGAG | 27342 |
| rs531107813 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767317 | CGAGGTTTTTTTTTT[C/G]TTTAAATCATAGAGT | 27342 |
| rs531129850 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786730 | ATGTTGTTTGCTAAT[A/G]TTTTTCTGAAGCTTG | 27342 |
| rs531133383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729912 | TGCAGCCAATGCCTG[C/T]GGATCTGTGGGTGGC | 27342 |
| rs531133902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723157 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 27342 |
| rs531151228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693107 | CTAGAAGCCCTGAGC[A/G]GGCTTCTTCATGGAC | 27342 |
| rs531198713 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800840 | GGGCGACAGCTGGTA[C/G]CGAGTGTTTGTGTGA | 27342 |
| rs531231194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764729 | ACTCTTCTTTTCTCC[A/G]TTGAGTAGTCTTGGT | 27342 |
| rs531233204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772385 | CCTGGTGAAGATTAA[A/G]TGAGCTAATAAATTT | 27342 |
| rs531252990 | snp | A/G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717127 | CCTGCCTTCTTTTGG[A/G/T]TTATTTGACTATTGC | 27342 |
| rs531267059 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682318 | TCTTGGGCCGGGGGT[A/G]GCGGGGCTGTTGGTC | 27342 |
| rs531296214 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760204 | TTGCCTTCGACACTC[G/T]TAACCTGGAAAAAGC | 27342 |
| rs531296366 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767258 | TCCACCCGCCTCAGC[C/T]TCCCAAAGTGCTGGG | 27342 |
| rs531308151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766793 | GCAGTGGTGCGATCT[C/T]GGCTTACTGCAGCCT | 27342 |
| rs531327504 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687643 | AATGAATAGGTGGAT[A/G]ACAGAGCCTTGGGAA | 27342 |
| rs531349401 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687869 | GGCGGGCAGATCCCT[G/T]GAGGTCGGGAGTTCA | 27342 |
| rs531368682 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773708 | TCTTGCTCTGTTACC[C/G]TGGCTGGAGTGCAAT | 27342 |
| rs531370331 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801355 | GGGGAAATGGGGTCC[A/G]TCCTCTGAAGCATTT | 27342 |
| rs531399308 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807155 | TGGCTGGCTTGCACA[C/T]ACTTAGCAGCTTCTA | 27342 |
| rs531408002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737265 | GTTTTTTTGGAGATA[A/G]GGTCTTGCTCTATTG | 27342 |
| rs531457635 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725164 | TATTTTCCCACTTCC[G/T]TACATGTCTGTACAT | 27342 |
| rs531482719 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780202 | TGTTCTTCTGAAGAG[G/T]CTTCAGTCCTCTGGC | 27342 |
| rs531514563 | snp | G/T | 0 | 0 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687182 | TCAGGCTGGAGTGCA[G/T]TTGCTCGATCTTGGC | 27342 |
| rs531517172 | snp | A/G | | | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757773 | CCTGCCACCATGCCC[A/G]GCTAACTTTTTGTAT | 27342 |
| rs531565128 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726960 | AGTGAGCCGAGATTG[C/T]GCCATTGCACTCCAG | 27342 |
| rs531578127 | snp | A/C | 0.000399281 | 0.0141238 | missense | RABGEF1 | GRCh38.p7 | 7:66809036 | TTAGGCGTCAAGCAA[A/C]TGTATAAGAACTTGG | 27342 |
| rs531579926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751657 | AGCAGGTACCCACCT[A/G]AGACTTTCAGCTGAT | 27342 |
| rs531582383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730778 | GGCCAGGCTGGCCTC[A/G]AACTCCTGACCTCAA | 27342 |
| rs531582859 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755772 | AGAGCGTGATCTAGT[A/C]CAATAGAAGACTGTT | 27342 |
| rs531603712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693909 | GCCTCTGGGGCTCAA[A/G]CGATTCTCCTGCCTC | 27342 |
| rs531610916 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773209 | AATCAAAGAGAGAAA[A/T]TTTTAGCCGAGAACA | 27342 |
| rs531641908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698852 | CCACCTTTCTAACCT[C/T]GGTTTTCCTCATCTG | 27342 |
| rs531670321 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779756 | GCCCTAGCCAAAATT[A/G]TGAACTGTAACGTGG | 27342 |
| rs531676316 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691928 | AAAGTGTGCTGGCAC[A/G/T]CATCTGTAGTCCCAG | 27342 |
| rs531687449 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761630 | CATTCGTCCCTCAGA[A/G]TACAGAGCTGGACCC | 27342 |
| rs531688085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786910 | TTTATGTTGAAAATA[C/T]AGTTGCCATCAGCTA | 27342 |
| rs531691271 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733053 | TCCAGCTCCTTAGCC[A/G]CGTAGTCAAGGTTCC | 27342 |
| rs531695291 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775565 | TGAAATCAATACTCT[A/C]TTTGGTTGAAAGACA | 27342 |
| rs531732276 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763934 | ATTATGGATAATGCT[G/T]ATATAAACATTCACG | 27342 |
| rs531736895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700978 | TCAGTGTGGTGGGCA[A/G]CGCTGTCTTGCAGCC | 27342 |
| rs531741032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788612 | GATAAGCTCTTCTTT[C/T]TAAGGAAGCAGTTAA | 27342 |
| rs531767349 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708079 | ATTAATCATAAGGAT[A/T]TACTTCTCCCAGTCT | 27342 |
| rs531801536 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787904 | TTTTTCTGTAAATTA[G/T]TTATATGAAAACGCT | 27342 |
| rs531854154 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66753351 | AACCCAGAGTTCGAT[A/G]TAAATTTGTGGAAAA | 27342 |
| rs531866975 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748325 | GTTTTAGATTATCTA[C/G]ATGAGTAGGTGGATT | 27342 |
| rs531882747 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706823 | GTCTTGCTCTGTCGC[A/C]CAGGCTGGACTGCAG | 27342 |
| rs531895565 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781183 | TAGCTATACCTCTTT[G/T]TTCTGTTTTGTTTTT | 27342 |
| rs531908361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794358 | ATGGGGTCTCACTAT[A/G]TTGCCCAGGCTGGCC | 27342 |
| rs531921080 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738016 | GGTTGTGTTTTTTGT[G/T]TTTTTTGTTTTTTTT | 27342 |
| rs531929922 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754728 | CCATCTAACAAATCT[A/G]AATAAATACATTTCA | 27342 |
| rs531945939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794968 | TCTATTTAAGAATAC[A/G]TAGATTTAGCAAAAA | 27342 |
| rs531947029 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741773 | CTGGCCTTAAGTGAT[C/G]CTCCCGCCTCGGCCT | 27342 |
| rs531976344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748938 | TCCAAAAACTGTTTT[A/G]TGTCATAAGAGCAAG | 27342 |
| rs531983125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743005 | TTTAGCTGGGTCCTT[A/G]TGTGGTTAAAATGGG | 27342 |
| rs531992788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687741 | ACTTTAGATACAAAG[A/G]CACAATGAGATTGAA | 27342 |
| rs532003165 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66682030 | CCTTTGGATCCCGCT[A/C]GCACTTCCTCCCGTC | 27342 |
| rs532012124 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807034 | AGCGAGTCAGACAAC[C/G]TGGAAGTCCCTGAGA | 27342 |
| rs532013663 | in-del | -/TGGCTCATCATCAGGGCCACC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729924 | CTGCGGATCTGTGGG[-/TGGCTCATCATCAGGGCCACC]TGGCTCATGGAGGCC | 27342 |
| rs532030485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687003 | ATTTTTTATATTTTT[A/G]GTAGAGACGGGGTTT | 27342 |
| rs532069920 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759745 | CAAGCACAGAACCAC[A/G]GGGGATGGTGCGAAA | 27342 |
| rs532080950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717748 | TGTATTTTTCAGAGA[C/T]AGGGTTTTGCTCTGT | 27342 |
| rs532083442 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773085 | TAGCTAGTTGTTTGT[G/T]TTTTTTTTTTCATCC | 27342 |
| rs532095801 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725017 | ATCTTCTATTTCTCT[C/G]CTTATTATATTTGTT | 27342 |
| rs532131247 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783988 | AGAAAAGCCTCTGAA[G/T]CAAGCTAAAACCCAA | 27342 |
| rs532142277 | snp | A/T | 0.0154783 | 0.0866001 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779671 | AGCGAGACCCTGATT[A/T]AAAAAAAAAAAAAAA | 27342 |
| rs532253324 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743474 | GGACCACAGGCCTGC[C/T]ACCTACTAATTTAGC | 27342 |
| rs532295817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746265 | GTTTTCAATGAAGTT[A/G]CTGTCAGTGGGATAG | 27342 |
| rs532296800 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66682027 | AAGCCTTTGGATCCC[A/G]CTCGCACTTCCTCCC | 27342 |
| rs532316185 | in-del | -/T | 0.470424 | 0.117954 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746790 | ACCACGTCCGGCTAA[-/T]TTTTTTTTTTTGCTG | 27342 |
| rs532347868 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792951 | GAGACAGTGGCAGGG[A/G]TGAGTTCTTTTACAT | 27342 |
| rs532362578 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772108 | CTAGGGGCGGTTGAA[C/T]AGTGACGTGACTGGA | 27342 |
| rs532379993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694717 | TCGGAATCTCGTGGA[C/T]TGGCCTTGGTCTACC | 27342 |
| rs532385622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736215 | TAGGTCTTCACCCAT[A/G]CACACACTTTCTCAG | 27342 |
| rs532412034 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705353 | GAGGCAGGAGAATCA[C/T]TTGAACCCAGGAGGC | 27342 |
| rs532433402 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700094 | GAGAGGGACAAGAGT[C/T]CTCAGCCCTGAGCAT | 27342 |
| rs532440005 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699689 | AGAGCAAAATTCCAT[C/T]TCAAAAAAAAAAAAC | 27342 |
| rs532448805 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704836 | AAAAAAGTTTAAATA[A/C]CCAACGTGTATCTTC | 27342 |
| rs532451204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737930 | GCATAGCAGCACAGC[C/T]GGCTCCCTCATCTTT | 27342 |
| rs532478789 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781046 | TTTAATGTGATTTTT[G/T]ATAAGGGAAGGTTTA | 27342 |
| rs532515804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774434 | AATCCAGAATAGTGG[A/G]CTCAGCAATCAAGAT | 27342 |
| rs532527319 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794187 | TCTGTGGCTCTGCTT[C/T]AGGTCTCTCTCCATG | 27342 |
| rs532544726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787810 | CACTGTATAGACCCA[A/G]TCAAGTGTTAACCTT | 27342 |
| rs532587696 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800745 | TTTTGTCCAAGCCAC[C/T]GTAGCCTTTACGGCC | 27342 |
| rs532621017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712303 | CATAAATATTTTGCA[C/T]GTTTTGCTAATTTTA | 27342 |
| rs532703988 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800404 | TCTTCCACTTTCTCG[A/G]GTTCTGCTTCTCTTT | 27342 |
| rs532704139 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-5-prime, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66682164 | AGCGGACTGGGGAAC[C/T]CAGACCTGCCGAGCG | 27342 |
| rs532707765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718533 | TCAAACATAGTGTTA[C/T]GTGGTTAAATTCTAT | 27342 |
| rs532715553 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742570 | AGGGAGAGGGGGGAA[C/T]CAAAGGAGAGGAGGC | 27342 |
| rs532731974 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712801 | TTCTTGAGATTTTTC[G/T]TTTTCTTTTTCATTT | 27342 |
| rs532789257 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754603 | AGCCCTTTTTCAGTA[C/T]ATTGGCCAGTCCAGC | 27342 |
| rs532794431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747688 | ATTTTCTAATTTTAA[A/G]CACTTTCATTTTTCC | 27342 |
| rs532804428 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749754 | AGGCGGGCGGATCAC[C/G]AGGTCAGGAGATAGA | 27342 |
| rs532806911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754002 | GAGCCAACGTACTAG[A/G]CCATTTTTTTTTTTT | 27342 |
| rs532855648 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693516 | GTGTCTGGTCCCCTG[A/G]CTACTCCTCCTCCCC | 27342 |
| rs532917336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721195 | AAGTGCTGGGATTAC[A/G]GGCATGAGCCACTGT | 27342 |
| rs532918090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789180 | AGTTTGCCCTGCCAC[A/G]TAATTTACTGTCAGA | 27342 |
| rs532936739 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719920 | TGCTGGTCCCTGATG[C/T]GGACCAGCAGTCTTC | 27342 |
| rs532950057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707910 | TAAAGCCAATTTTTT[C/T]CTGACATTAATATAG | 27342 |
| rs532980473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795713 | TCATCCTGTAACCTC[A/G]TGGACATTCTGGGAA | 27342 |
| rs532982226 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703254 | TGGGATTACAGGTAT[C/G]AGCCACCGTGCCTGG | 27342 |
| rs532996394 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, missense, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756073 | GGCGTCTTCATACCA[A/T]GAAGGTGAGTACTGA | 27342 |
| rs533032867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726111 | TACTCAGACAGGGCC[A/G]GAAGGGATGCCAGGC | 27342 |
| rs533035893 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726985 | CTCCAGCCTGGGTGT[C/T]GCAGCAAGACTCCAT | 27342 |
| rs533036419 | in-del | -/TGGCAGGTGATGAGGGTG | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736608 | AGAATGGGTAGGACT[-/TGGCAGGTGATGAGGGTG]TGGCAGGTGATGAGG | 27342 |
| rs533064057 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762333 | CAGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT | 27342 |
| rs533086202 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802234 | TGTGGGAGTACTACT[A/C]ACACCTAGTGGGTAG | 27342 |
| rs533127453 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715052 | ACTACTTCTTCTCCT[C/T]CTCTTTCTCTTTTTC | 27342 |
| rs533158566 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801825 | TGACTTCTGTGTGGC[A/T]ATGGGGGCAGTGGTT | 27342 |
| rs533182455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803235 | CCTGTGCACTGCCTA[A/G]CACATCTGTCCCCCA | 27342 |
| rs533196858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757069 | TTTTGTTGAGTTCCA[A/G]AAAGTCTTGTGGGAT | 27342 |
| rs533213466 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684710 | CCTGATCTTGGCTCA[C/G]TGCAAGCTCCGCCTC | 27342 |
| rs533223461 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682827 | AGGGCGAGGCTGCGG[G/T]GCCGGGGTTAGGAGC | 27342 |
| rs533240276 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810617 | AGAACCTTTTCTTAT[A/C]TCAGTGGAACCTTCT | 27342 |
| rs533242967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770903 | TCACATTTGTTGGCT[A/G]TTGGTATGTCTTTGG | 27342 |
| rs533244841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763260 | GAGGTCAGAATTAAG[C/T]ATCGGCCAGCCTGGG | 27342 |
| rs533253066 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770024 | GGTCTCTCTATACTC[C/T]GTAAGTGAGAATTCC | 27342 |
| rs533268997 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774943 | GTTTACTTACCTTTT[C/T]GTCTGTTCCAGCCTT | 27342 |
| rs533270983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767479 | GTCACATTCTTTCCT[A/G]CCCCTAGTTCCTAAA | 27342 |
| rs533298341 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695298 | GCCTGAGCAGCAGAG[A/C]GAGACCCTGTCTCAA | 27342 |
| rs533317779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721939 | GAGGATCACTTTGAG[A/G]TCAGTAGTTCAAGAC | 27342 |
| rs533342284 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690378 | TGCTGGGATTACAGG[C/T]GTGAGCCATCGCGCC | 27342 |
| rs533357957 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803799 | GAGGCTGAAGCAGGA[C/G]AATCGCTTGAACCCG | 27342 |
| rs533405190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721279 | GAATAAATTTAATAA[A/G]AGACATGTATATTAG | 27342 |
| rs533422051 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739430 | GAAGCCAAGGTGGGC[A/G]GATCACTTGAGGTCA | 27342 |
| rs533422710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775833 | TTATTTGAGAGACAG[C/T]TTGTGTCTTGAGGAA | 27342 |
| rs533426084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695954 | GTGGGTAACAAAGCG[A/G]GACTGTCTCAAAAAA | 27342 |
| rs533442835 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793937 | TGGGGGTTTGTTCTC[A/G]GCCTTATTCATGTTC | 27342 |
| rs533489127 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727959 | TGCCTCAGGCGTCTC[C/T]ACCAACCTCATCCTC | 27342 |
| rs533495275 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782840 | TCGTTTTGGAAATCA[C/T]TGGGATATGGGGAAC | 27342 |
| rs533508999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691267 | TAATTCTATATATTC[C/T]TAGGCATTTACTCAA | 27342 |
| rs533530454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725360 | CCTTGTCCCACAGTC[C/T]CTCCATTCTGCCCCA | 27342 |
| rs533531884 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734033 | AAAAAAAACCTCCTA[C/G]AGGCAGTCATCAGCC | 27342 |
| rs533545248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696428 | GGCGTGGTGGCTCAC[A/G]CCTGTAATCCTAGCA | 27342 |
| rs533568586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745708 | CGGGAGGCGGAAATT[A/G]CAATGAGCCGAGATT | 27342 |
| rs533571562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787450 | CCAGGTTCAAGCAAT[C/T]TTTATGCCCCAGCCT | 27342 |
| rs533572507 | snp | C/G | 0.00199481 | 0.0315187 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740020 | CTGCTGTCACCCGGC[C/G]TGGAGTTCAGTGGAG | 27342 |
| rs533604961 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776961 | ACAGACTAACCTCTC[C/T]GAGTCCTGTCCACAC | 27342 |
| rs533635693 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702237 | TATCAAAATTTCATT[C/G]CTCTTTAGGGTTGGA | 27342 |
| rs533650883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747878 | GGGTTTGTAATGACT[C/T]ACAAAGATACGTGCG | 27342 |
| rs533652657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754190 | TGTATTTTTAGTAGA[A/G]ACGGGGTTTCACTAT | 27342 |
| rs533655447 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783478 | AATGTAGTTTTGTCT[A/G]CTCATACTTCCTACT | 27342 |
| rs533673212 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701618 | GGTTCAAGCAATTCT[C/T]CTGCCTCAGCCACCC | 27342 |
| rs533681852 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793817 | CCTGCCATCCTTTTA[C/G]AGTTAAGCCAGATGG | 27342 |
| rs533702036 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792147 | TAGAAAAGATGATCC[C/T]GTACAATGATTAGAG | 27342 |
| rs533709719 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760250 | ATATCTGTGGTTTTG[A/T]CATTTGGAAAGGTTG | 27342 |
| rs533738177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788107 | CAGGCTCTACTTCCT[C/T]AAAGTACCTACCCTT | 27342 |
| rs533758278 | snp | A/G | | | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756129 | AATCAAAAGAAAATA[A/G]TAATGACATAGAAAA | 27342 |
| rs533788796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718025 | TGAGGGTTTCTATCA[C/T]TCCATTCATTTAAAA | 27342 |
| rs533796851 | snp | C/T | 0.00755907 | 0.0610114 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66682051 | TCCTCCCGTCATCAG[C/T]CAAAGGCCCCGGAAG | 27342 |
| rs533819162 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759890 | ACATAGGCATATAGT[C/G]CCTTTAAAACTGATC | 27342 |
| rs533824176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724566 | GGTTTCACCATGTTG[A/G]TCAGGCTGGTCTTGA | 27342 |
| rs533891155 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712531 | GCTGGAGTGCAGTGT[C/T]GTGATCACAGCCCAC | 27342 |
| rs533902852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706126 | CCAGGATGGTCTCGA[C/T]CTCCTGACCTCATGA | 27342 |
| rs533942205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718697 | TGTCCTGAGTATGTA[C/T]CACGCAGTGGCCAGC | 27342 |
| rs533974928 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713277 | CTCCCGAGTAGGTGG[G/T]ACTACAGGTGCCCGC | 27342 |
| rs533985092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793280 | GGACCCAAGTCCAAA[C/T]ACAGAATTCATTTGT | 27342 |
| rs533986703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799974 | GCCTCCTAATAAGGT[C/T]TGTTTCTCATTCATG | 27342 |
| rs533999947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801295 | TTATTTATGAGTTCC[A/G]TGAGCTATTTTGATC | 27342 |
| rs534016765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719568 | CTGGTAAATCCTTTC[A/G]AATAATTAAGGAGGG | 27342 |
| rs534063707 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681429 | TTTGAGACAGGGTCT[C/G]GCTCTGCTCTGTCAC | 27342 |
| rs534064616 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682964 | AGGCAGCTGGCGGTG[A/T]CTCAGCGCGAGTGAC | 27342 |
| rs534067560 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709078 | GCTAGAGCGCAATGG[C/T]ACAATCTCGGCTCAC | 27342 |
| rs534080110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761047 | CTTCTTTCAACAAAG[A/G]ATTGAGAACCTGTGA | 27342 |
| rs534109053 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705059 | GCTGATGTAAATGGG[A/C]ATGTATTTTTCACTT | 27342 |
| rs534110018 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785602 | CTTTGTGGCCGGGTG[C/T]GGTGGCTCACGCCTG | 27342 |
| rs534131341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687343 | GTTGGCCAGGTCAGT[C/T]TCAAACTCCTGAACT | 27342 |
| rs534134548 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681725 | AACTCGAACACCTGT[C/T]ACATCCTAGGATCCG | 27342 |
| rs534139177 | in-del | -/CACA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786456 | TCTCCTGGACTGGAG[-/CACA]ATAGCGCAGTTGCTG | 27342 |
| rs534175408 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751133 | CTCCCAGGTTCAAGC[-/A]AATTCTCCTGCCTCA | 27342 |
| rs534203815 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66685790 | TACCTATGTCAGTCT[C/T]TGGCTAGAGACATAG | 27342 |
| rs534225656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694538 | TGAGCTAAAGAGGGG[C/T]ACGGTCAGGTTTGCA | 27342 |
| rs534250795 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781287 | TAGAAAAAAGAAAAA[A/T]AAATTAAAACAGTAG | 27342 |
| rs534264671 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781333 | CATAAAATAATCTTA[G/T]ACGGGAATTTTTAAA | 27342 |
| rs534270576 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755042 | GCTCACACCTGTAAT[C/T]CCAGCACTTTGGGAG | 27342 |
| rs534279199 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727030 | AAATAAAATATAATA[C/T]GGACTGTGGAAATGA | 27342 |
| rs534282219 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769798 | TGTAGCTTAGAGTTT[C/T]AAAAAGCCATCATGA | 27342 |
| rs534284164 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728033 | TGTCCCCCTTCCACC[C/T]TTCCAGTGTAATTCT | 27342 |
| rs534285005 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761848 | TTGACGTCAGGAGTT[C/G/T]GAGAGCAGCCTGGCC | 27342 |
| rs534320134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734242 | GGCAAGGAGAGGCAC[A/G]GGTTATCGGTGTCTG | 27342 |
| rs534320174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727761 | TGGCAGGCTGCCCGT[A/G]GATAATGGAAAAGTC | 27342 |
| rs534348994 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768209 | TGGACAGTTAACAAA[G/T]TGTCTTCTGCTGTGG | 27342 |
| rs534363121 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720264 | GTGCAGTGGCGCGAT[C/T]TCGGCTCACTGTAAC | 27342 |
| rs534365582 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810150 | TGGGCCTCTGATGGT[C/G]AGAGGTGACGGGGTC | 27342 |
| rs534366739 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694040 | TCTCGAACTCCTGGC[C/T]TCAAGTGATCCACCC | 27342 |
| rs534396429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732388 | CCCACCACCCACCAA[A/G]AGGTGAGGAGAAGCA | 27342 |
| rs534397833 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717965 | TGTATATTATCAGTT[C/T]TAAAATATCTATTTG | 27342 |
| rs534419507 | in-del | -/T | 0.130351 | 0.219509 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693811 | CTTTCCTTTTTTTTC[-/T]TTTTTTTTTTTTTTG | 27342 |
| rs534470027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694955 | GAGCCCTGTTGAGGA[C/T]GAGGCTGGTGACCCA | 27342 |
| rs534486618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731945 | CCCCCTGTCTCCATC[C/T]ACTCCCCCCAGGGCC | 27342 |
| rs534508124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695687 | TTGTAGACAACTGGC[C/T]AGGCGCAGTGGCTCA | 27342 |
| rs534534278 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708197 | TTCCTTGTTGTTACT[C/T]TTACTATATATTTTT | 27342 |
| rs534536346 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786946 | CTGTTCTTACAAATC[A/C]TCATAGCAAGAATTT | 27342 |
| rs534542119 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701249 | CAGGCCTGTAATCTC[C/T]ACGCTTTCAGAGGCT | 27342 |
| rs534547578 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716654 | ATGTATAGTCATGTC[-/T]TTTTTTAAAAAAAAC | 27342 |
| rs534555389 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750735 | TCAGCCAGTTGGACT[A/G]CAGGTCCAACCAGTT | 27342 |
| rs534576960 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691649 | TTCAATTTCAGTAGC[A/G]TATCCAATAAATTAC | 27342 |
| rs534587071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684260 | ACCAGCCTGACCAAC[A/G]TGGTGAAACCCCGTC | 27342 |
| rs534592980 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810791 | TCTTGCTTTTCCAGT[A/G]TCTTCCTAAGGATGG | 27342 |
| rs534617341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707580 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 27342 |
| rs534630925 | in-del | -/TTGA | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764603 | TTTACATTTAGGTCT[-/TTGA]TTGATTCTGAGTTAG | 27342 |
| rs534653260 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777675 | CTACCTACCTATAAT[C/T]CCAGCTACTTGGAAG | 27342 |
| rs534669318 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690880 | CTTGAGATCAGGGGT[C/T]GGAGACCAGCCTGGC | 27342 |
| rs534745430 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694513 | GCAGTGGGAAGCCAG[A/C]AAAGGGCATTGAGCT | 27342 |
| rs534752711 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775988 | AATGCCATATAACCA[G/T]CAAGAGGATTGTCAC | 27342 |
| rs534806750 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701886 | TTTTTTTATTGATGA[C/G]TGTTTTTAAAAATTG | 27342 |
| rs534829777 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782522 | CCCAGGCTGTGGAGT[A/G]TAGTGGGATGATCTC | 27342 |
| rs534861192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715866 | TCAGGTGCTCCTTGT[A/G]CCTCCGCCTCCTGAA | 27342 |
| rs534913334 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749946 | ACCACTGCACTCCAG[C/T]GTGGGCGACAGAGCG | 27342 |
| rs534914390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751109 | GATCTTGGCTCACTG[C/T]AACCTCCACCTCCCA | 27342 |
| rs534916553 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738175 | ACAGGTACAGGCCAC[A/C]ACCTGGCTAATTTTT | 27342 |
| rs534926028 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749390 | TGTGTTTCCTTAATT[C/G]TATATCCATAAAGCT | 27342 |
| rs534952085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795835 | CATTGGGGCAGGGCT[A/G]GAGCTGACGAAAACA | 27342 |
| rs534957056 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692975 | CCCCCCATGCCGGAA[A/G]GGGCTGGCACCTCCC | 27342 |
| rs535007600 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697319 | GGGGCTTGCAGCGTG[A/G]CGTCTCACAAGTCTT | 27342 |
| rs535044326 | snp | C/T | 0.000798881 | 0.01997 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703428 | CAATTTTAGCTCTCA[C/T]AGTTAGGTCTTTTAT | 27342 |
| rs535048953 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808801 | GCTTCTGTTTTAAAT[C/G]GTCTGTGATCAAAAG | 27342 |
| rs535052470 | in-del | -/CC | 0.00716266 | 0.059414 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721641 | TGCAGTGGGACCTAT[-/CC]AGATAATCCAGGATA | 27342 |
| rs535064990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768332 | GACACCAGTGTATAT[A/G]TCTTCTTTGTTAAAG | 27342 |
| rs535074105 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727350 | CTGGACTCAGGGCCT[A/G]GGGCTTCCTCCAATA | 27342 |
| rs535111373 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732922 | CCAGGCTCGCCCTGC[G/T]TCTCTAAACTTCTCG | 27342 |
| rs535123164 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739510 | AATACAAAAAAAAAA[A/G]TATGAGCTGGGCGTG | 27342 |
| rs535125791 | snp | C/T | 1.65002e-05 | 0.00287225 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66775343 | AGACCCGCAAGGTTA[C/T]CACAGTGAAGAAATT | 27342 |
| rs535145705 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692819 | ATGGAGACTCCAAAA[A/G]AGGAAGTGATTCCAC | 27342 |
| rs535183026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708914 | TGGGAGGGGGATAGG[A/G]AAAAAAAGAAATATG | 27342 |
| rs535194788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743588 | CTCACTGCAAGCTCC[C/T]CCTCCTGGGTTCACG | 27342 |
| rs535225573 | snp | A/T | 0.000109772 | 0.00740771 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797335 | AAGAGAGAGAAAAAA[A/T]ATATATATCTTGATC | 27342 |
| rs535243007 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803958 | TTTTGAGATTAAGTT[A/T]ATTCCCTTGCTTGAT | 27342 |
| rs535261345 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759903 | GTCCCTTTAAAACTG[A/G]TCACCGTTACAGCAA | 27342 |
| rs535265947 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731007 | GACAGCGCAGGGATT[C/T]GGGGCCAGGCTGCGG | 27342 |
| rs535288186 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784710 | AAATAATTTTTAGAT[A/G]TTGAATTCAGTTTGT | 27342 |
| rs535290933 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700681 | ACTTCTGCCACTCAG[A/C]TCTCTTCACACCACC | 27342 |
| rs535297738 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743198 | CGTAATGCTAGCTAC[A/T]CAGGAGGCTGAGGTA | 27342 |
| rs535302251 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721508 | TCCTCCATCATTAAA[C/T]GCAACAGTGCAGCAT | 27342 |
| rs535329313 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763377 | CCTCATTTCTTTGTT[G/T]GCTGTCAGCCAGAAG | 27342 |
| rs535344597 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711124 | GTGATTGCACCACTG[C/T]ACTCCAGCCCGGTTG | 27342 |
| rs535354187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794733 | CCACTTTTGGAAATG[C/T]ATGACAGAGAACCGA | 27342 |
| rs535382294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748688 | AAGAATTTCCTTTTC[C/T]ATTGCAGTCCTGAAG | 27342 |
| rs535394346 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754987 | CGAGACCAGCCTGGG[A/C]AATATAGCTAGATCC | 27342 |
| rs535399611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733647 | AAGTTGCAGTGAGCC[A/G]AGATCGTGCCACTGC | 27342 |
| rs535427390 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689672 | GTTGGGCATGGTGGT[A/G]GGCACCTGCAATCCC | 27342 |
| rs535449747 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783943 | TGCCTGAGAAAAATC[A/C]AGACCAAGAGATGTT | 27342 |
| rs535464811 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782961 | AAGCACTTACTGCCT[G/T]TTACAACATCCTTAT | 27342 |
| rs535473047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790852 | AGGCCAATAGGACAC[C/T]ACAGGTCTTCTAGAG | 27342 |
| rs535492436 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713989 | TTTTTGAGTTTTTTT[C/G]GTCTATGTTCATAGA | 27342 |
| rs535515381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695608 | GTGGGTCGTGAGAAA[A/G]TGAGGGATTAGAAGT | 27342 |
| rs535537538 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793363 | AGCAGTTTTGTGCAT[A/G]TAACAGTTTTGGCTG | 27342 |
| rs535561309 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757156 | CATTTATTTTCACAC[A/G]TTATGTTAAGTATAT | 27342 |
| rs535569516 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789665 | TCCAGCCTCAGCATC[A/G]GAGCGAGACTCTATC | 27342 |
| rs535578525 | snp | A/C/G/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782493 | TTTGGAAGAGACAAG[A/C/G/T]TCTCATTCTTTCGCC | 27342 |
| rs535584955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750250 | CACTTTTTAATACCA[C/T]CTATGAGAAATTCAA | 27342 |
| rs535588055 | snp | G/T | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681232 | CTGCACCTTTCACCA[G/T]AGATGGCATCCAGGA | 27342 |
| rs535600297 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721606 | CTGACCCTCCTGCCT[-/C]CCCCCCTTATGAGAA | 27342 |
| rs535650999 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788239 | ATCACGAGGTCAGGA[G/T]TTCGAGACCAGCCTG | 27342 |
| rs535673590 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749345 | AACAGTGGGTGAAAC[A/T]GCCCTTGCCTAAATA | 27342 |
| rs535684368 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799983 | TAAGGTTTGTTTCTC[A/G]TTCATGGGAATGAAC | 27342 |
| rs535709199 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801876 | CCCCCGGAGACATTG[A/G]ACAACATCTGGAGAC | 27342 |
| rs535734876 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749913 | TGGGAGGCGGAGCTT[A/G]CAGTGAGCCGAGATC | 27342 |
| rs535736893 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755710 | TTGAGCTGTTATTCC[G/T]GAGAATGGCATGCTC | 27342 |
| rs535744581 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745287 | CTTTGGCTAGAGACA[C/T]AGAATTTCAGTCTTG | 27342 |
| rs535759774 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725634 | GGCAATTTTATGAGG[C/T]AGATATGACTCCCCC | 27342 |
| rs535773532 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782672 | AGAGAGCAGCTACTC[A/G]GAGACTTGAGTAGCT | 27342 |
| rs535853596 | snp | G/T | 1.65559e-05 | 0.00287709 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805134 | ATTGTCTTTTCTGCT[G/T]TGTAGATATCATTGA | 27342 |
| rs535883746 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680976 | TAATTCCGGCTACTC[A/G]AGAGGCTGAGGTGGG | 27342 |
| rs535885056 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716114 | TATTTGAGGTCTGTT[C/T]TTAGATGTGTACACA | 27342 |
| rs535908799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796441 | TCTTGGGAGTTGCAA[A/G]TGCCTTTGTAATGTA | 27342 |
| rs535910389 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723239 | CTCCCAAAGTGCTGG[A/G]ATTACAGGCATGAGC | 27342 |
| rs535914880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804249 | TTACCACACTCGGCT[A/G]ATTTTTGTATTCTCA | 27342 |
| rs535920053 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686029 | CACGCCTGTAATCCC[A/C]ACACTTTGGGAAGCT | 27342 |
| rs535939573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750960 | TACTTTTCAGATCTA[A/G]AATTTCAGTTTGACA | 27342 |
| rs535974514 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715153 | CTTCTCCTGAGACAG[C/G]GTCTCACTCTATCAC | 27342 |
| rs536016409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721394 | GTCAGTCTGTCTGAA[A/G]TCAAGATGTCACAGA | 27342 |
| rs536016420 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714662 | AATTTAGGGCCAGGC[A/G]CAGTGGCTCATGCCT | 27342 |
| rs536020649 | snp | C/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758690 | CTGGGTGTGCCGACT[C/G]TCCTGCCTTCTACCG | 27342 |
| rs536037328 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803325 | ATGATCTAAAAGCTG[A/G]AAGAACCCTTTGGTA | 27342 |
| rs536094839 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810644 | TTCTATAACCTAAAT[A/G]TACCATTGATGATTC | 27342 |
| rs536099452 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684174 | TCCCTGGCTAGCTGC[A/G]GTGGCTTATGCCTGT | 27342 |
| rs536130186 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727741 | CACACCTGGGGAACC[A/G]TGAGTGGCAGGCTGC | 27342 |
| rs536167786 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703387 | AGGTCTTGGAGATTT[A/C]CCTCTGTTTTCTTCT | 27342 |
| rs536170743 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784559 | ACTCAGAATTAGCTC[C/T]GAAAGTTCCTTCTAT | 27342 |
| rs536177743 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745109 | AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCG | 27342 |
| rs536186800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776785 | GCAATTTTATCTCTA[C/T]GAAAAAGGGGGGAAA | 27342 |
| rs536203864 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688337 | TCATTGGTGACCTCA[C/G]TACCTCAACTTTATA | 27342 |
| rs536206622 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704667 | TACAAACAAATTAGC[C/T]GGGCGTGGTGGTGGG | 27342 |
| rs536212197 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730872 | CAGCACTTGGTTTCA[A/G]TTCTCACTTGTGAGC | 27342 |
| rs536214783 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737285 | TTGCTCTATTGCCCA[A/G]GGTGGAATGCAGTGG | 27342 |
| rs536223756 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758663 | ATGCTGTCTGTAGCT[C/G]TGATGTCCAATCTGG | 27342 |
| rs536296212 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680490 | CTCAGGTGATCCGCC[C/T]GCCTCTGCCTCCCAA | 27342 |
| rs536305596 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736354 | TCACATATGAGGTAG[A/C]GGTGGTGATGGATAG | 27342 |
| rs536335657 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758085 | TTGATTGGATGTTTC[C/T]TGTAAGTCCCAGATG | 27342 |
| rs536357413 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698109 | GCCACGCACCCCCCC[A/C/T]ACCCTCAGACCAGTA | 27342 |
| rs536373331 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749022 | GGCCTTCAGGCTCAC[C/G/T]GTGACTTCCTCCACT | 27342 |
| rs536381594 | in-del | -/ATT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720194 | ATTATTATTATTATT[-/ATT]TTTTTTTTTTTTTCT | 27342 |
| rs536386421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66685486 | ATAGCAAGACTGCAT[C/T]TCTACAAAAAAAAAG | 27342 |
| rs536404937 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771398 | CCCTCCTCAGCCTCC[C/T]AAAGGGCTGGGATTA | 27342 |
| rs536415196 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728715 | CTCAACTTTCAGCTC[C/T]GTCCTCACCTCCACC | 27342 |
| rs536478716 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746559 | CTCCCAAAGTGCTGC[A/G]ATTACAGGCGTGAGC | 27342 |
| rs536482038 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66740959 | TCGTCCCACATTCCG[A/T]CTCCGTCAGCGCCGC | 27342 |
| rs536564614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709988 | TTAGTGGAGAAAATA[C/T]TTTATTTTGCTTTCA | 27342 |
| rs536571802 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740301 | ACACCTGTCACATCC[C/T]AGGATCCGCGAAGGA | 27342 |
| rs536608078 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765663 | ACTGTCCTGATACTC[A/G]GACCACTTGATAGAA | 27342 |
| rs536611364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722311 | CAGGCGTGGTGGTGC[A/G]CGCCTGTAATCCCAG | 27342 |
| rs536624651 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66685448 | TCACTTGAGGCTAGG[A/C]GTTGGAGACCAGCCT | 27342 |
| rs536635113 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686786 | CTGTCAGTGGGATAG[G/T]AAGTCTAATTTTTAT | 27342 |
| rs536654380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730311 | CTGTTTCTGCTGAGC[A/G]CCAGCTTCCTCATCT | 27342 |
| rs536697908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721612 | CCTCCTGCCTCCCCC[C/T]TTATGAGAAACTTTG | 27342 |
| rs536703324 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810810 | TCCTAAGGATGGAGC[A/C]CAAAATTGCAGAGCA | 27342 |
| rs536739520 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711896 | CGGACTGTATACTCT[A/T]TTCTTTTGCATTGAT | 27342 |
| rs536775338 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779294 | GGATCACCTAAGGTC[A/G]GGAGTTCGAGACCAG | 27342 |
| rs536782177 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766267 | TGAGCTGTGATCACG[C/T]CACTGCACTCTAGCC | 27342 |
| rs536784206 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777610 | TTTACAATTCAATGC[A/G]GAGTCTGTACTTTAA | 27342 |
| rs536833528 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785881 | TCCATCTGGGGGGGA[A/T]AAAAAAAAAGTCTTT | 27342 |
| rs536839841 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696685 | ACAGGGCGAGACTCC[A/G]TCTCAAAAAAAAAAA | 27342 |
| rs536874921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702627 | CCGATTTCTCCAGAC[C/T]CTCAACAAAATTTAT | 27342 |
| rs536879259 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766189 | AAAAAAATAACAACA[A/G]TTAGCCAGGCATGGT | 27342 |
| rs536883427 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792982 | TATGAAAGCAATACT[C/G]TACTGGAGCATAAAC | 27342 |
| rs536886477 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704457 | TGCCTATCTATTTTC[A/C]CAAGTGGTTGTATCA | 27342 |
| rs536919393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791680 | CTGGAAGTGGAAACA[A/G]AGATCTCAGCCAGAC | 27342 |
| rs536940211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752646 | TATAGCAGTGGTTCT[C/T]AAAGGTAGTTCCTAG | 27342 |
| rs536984532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790205 | AAGAAATTAAAGACA[A/G]TAACCCTCACCTGAA | 27342 |
| rs537009756 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772163 | TACATTTTTTCACTT[C/G]TGCTTTGAGCTATCA | 27342 |
| rs537010135 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764200 | TCTCATTGTGGTTTC[A/G]TTTTGCACTTCCTTG | 27342 |
| rs537013390 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779283 | CCGAGGCAGGTGGAT[C/G]ACCTAAGGTCGGGAG | 27342 |
| rs537029751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736316 | AAAGCAAGGACAGGA[A/G]TGTTCCTTTAGCAAA | 27342 |
| rs537089466 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741485 | GGAGGGACTCTGCCG[C/T]TTTGGAGGCTAGGTC | 27342 |
| rs537199612 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776601 | CCAGAAGGCTGAGGC[A/G]GGAGAATCATTTGAA | 27342 |
| rs537222471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734382 | TGGGTAAGATGCTCA[C/T]CCTCTTTGAGCCTCT | 27342 |
| rs537243870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709961 | GCAGTTCTACCAAAA[C/T]AATAAAGTTGTTTAG | 27342 |
| rs537250222 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798262 | GGCTCACTGGGGTGA[A/G]CCCCAGCACTGTGTA | 27342 |
| rs537276018 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745272 | TTTACTTATGTGAGT[A/C]TTTGGCTAGAGACAT | 27342 |
| rs537282268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716516 | TGAGGCATGAGGATC[A/G]CTTGAACCTGGGAGG | 27342 |
| rs537294845 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744477 | ATCAAGACCATCCTG[G/T]CTAACACGGTGAAAC | 27342 |
| rs537333294 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758522 | CGATGTGTGGCCCCT[C/T]GGAGCTCCCTCCTGG | 27342 |
| rs537341996 | in-del | -/AG | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721858 | TTGGTGCTTTGAAAC[-/AG]AAAGTTTTTGGCCAA | 27342 |
| rs537347332 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789830 | GTGGTGGCTCCATGC[A/G]TGAGGCTGGTGCCAT | 27342 |
| rs537356791 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750852 | AGCAGACGCTTTATG[A/T]GTATTTGGAGAAGAA | 27342 |
| rs537436707 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706022 | ATTCTCCTGCCTCAG[C/G]CTCCCGAGTAGCTGG | 27342 |
| rs537436829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693010 | GGGGATCTTTTCTAG[A/G]GGCCCAGGCCCTCCT | 27342 |
| rs537438046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793785 | GGAATGAGGTGACTG[C/T]TCCTGACCCCAAGTG | 27342 |
| rs537450335 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793148 | GTTTCTAGTTGGAAG[C/T]GAGCACTACAGGTTG | 27342 |
| rs537473173 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747234 | ATGTGTTCATGAATG[C/T]GTAAAATATTACACA | 27342 |
| rs537479407 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774764 | CACTCTGTCTCAAAA[A/G]CAACCAAAAAAAGGA | 27342 |
| rs537481288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712037 | ATGTGAGTCCTCCAA[C/T]TTTATTCTTATTCAA | 27342 |
| rs537494376 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735711 | TCCCTTTGCTATGGC[C/T]ATGTGAAGACGTGCC | 27342 |
| rs537511728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697721 | TCCGGCCTCAGCGAG[A/G]TGGGGGGTGTTCATG | 27342 |
| rs537534724 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66753389 | CTTCTAATTATTTGT[A/G]GAGTTTACAACAATT | 27342 |
| rs537549330 | snp | A/T | | | intron-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811905 | ACAAATGATAGCTAT[A/T]ATTTGTAGATGGTTA | 27342 |
| rs537550699 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759782 | ATGATTAACTGCCCC[A/G]TGATCAGATCACCTT | 27342 |
| rs537568407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785499 | TCTTTACACCTGAAC[C/T]AACATAACTAGCTTC | 27342 |
| rs537615264 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766072 | GATTAGCTCAGACTT[G/T]CAAAATAATTTGAAA | 27342 |
| rs537619766 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806766 | CTCATGCCTTAGCCT[A/C]CCAAGTAGCTGGGAT | 27342 |
| rs537647588 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742462 | CCGGGCATTTAGGCC[A/G]TGCTGTTGGGTGTGG | 27342 |
| rs537668422 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681652 | CAAGCGATCCTCCTG[C/T]CTGGGCCTCCTAAAG | 27342 |
| rs537674232 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691040 | GGGTTGCAGTGAGCC[A/G]TGATCGTGCCACTGC | 27342 |
| rs537706303 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686688 | TGATGTTGGATAAAG[C/T]TCCTAAAATGCTGTA | 27342 |
| rs537760582 | snp | C/T | | | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760683 | TCCTGACCATGTGAT[C/T]TGCCCGTCTCAGCCT | 27342 |
| rs537814903 | in-del | -/T | 0.000980022 | 0.0221145 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771834 | ATTGGTAAGATTTTA[-/T]TTAGTAGAATGATAA | 27342 |
| rs537820093 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727710 | CGCAGGGGTCCTGGC[A/G]GTGGCCAGAAGTGGG | 27342 |
| rs537832531 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801189 | GAGTTTAGGACAAGG[A/G]GAGTGTCAGGGCCTG | 27342 |
| rs537854422 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748843 | TTTCTGATTAGACCA[A/G]TCTGTTTGCAAGTCT | 27342 |
| rs537891426 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808348 | AGTCTCCCAGGTAGC[A/G]GGGATTACAGGCGCC | 27342 |
| rs537895413 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718984 | CTTTCTTCAGTGCCA[A/T]GTGGCAAGAGCATAG | 27342 |
| rs537903550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807517 | TTCCTGCACCATCTT[C/T]TCTGTCACAGAGCTG | 27342 |
| rs537906306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682561 | GCCGCCTCCCTGTCC[A/G]GCGGCTCCCCTCGGT | 27342 |
| rs537934718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725482 | GACTTAGCATCATGT[A/G]TTCAGAGTCCATCCA | 27342 |
| rs537969754 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688873 | CGAAGCGGGAGGATC[A/C]CCTGAGGTCAGGAGT | 27342 |
| rs537989081 | snp | A/C | 0.00755907 | 0.0610114 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66682046 | GCACTTCCTCCCGTC[A/C]TCAGCCAAAGGCCCC | 27342 |
| rs537996137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717304 | AGGAACCTGGCTATC[A/G]TGTAGGTTCCTTTCC | 27342 |
| rs537998037 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708531 | TGACCTCAAGTGATC[C/T]GTCCACCTCTACCTC | 27342 |
| rs538014215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773908 | TGAGCTCAAGTGATC[C/T]GGCCGCCTTGGCCTC | 27342 |
| rs538025508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799123 | CCTTCCATTCTTGTG[A/G]TAAATGCAGAAGTCT | 27342 |
| rs538033310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694485 | CCACAGAGGGCCCGG[C/T]GGGGCCTGGAGGGCA | 27342 |
| rs538083955 | snp | C/T | 0.149665 | 0.228982 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723831 | GTGATCTGCCCACCT[C/T]AGCCTCCCAAAGTGC | 27342 |
| rs538087443 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805945 | AGATGGGGTCTCGCT[C/G]TGTTGCCCAGGCTGG | 27342 |
| rs538119763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694097 | TACAGGCGTGAGCCA[C/T]TGCACCCAGCCTTGT | 27342 |
| rs538156460 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699095 | CCTTGGGAGGGTTGG[A/C]CTTGGTAACCTGTGG | 27342 |
| rs538162686 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776570 | CAGTGGCATGTGCCT[G/T]TAGTTCCAGCTGAGG | 27342 |
| rs538175227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787396 | TTGCCCAGGCTGTAG[C/T]GCAGTGGCGTGATTT | 27342 |
| rs538177547 | in-del | -/C | 0.0667028 | 0.170006 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698101 | CATCACAGCCACGCA[-/C]CCCCCCCCACCCTCA | 27342 |
| rs538182256 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686129 | TACTAAAATACAGAA[A/G]ACTTAGCCAGGCATG | 27342 |
| rs538212041 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717305 | GGAACCTGGCTATCA[C/T]GTAGGTTCCTTTCCC | 27342 |
| rs538215904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760962 | TATTTATTAAGCGTT[C/T]AGTACGTATCATTGC | 27342 |
| rs538241969 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725975 | AGAAAACCCCCATTC[A/G]TCAGGCCTCCCTTGA | 27342 |
| rs538246822 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799639 | CGTTTCTTGGGCATT[A/T]AACTAAACTAAGGTC | 27342 |
| rs538249238 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739908 | AATCAGGTAAACAGG[A/C]TTCAATTTGTGACTC | 27342 |
| rs538257963 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714611 | TTGTGCTTACCTTGG[A/G]TTGATTTTACTCTTT | 27342 |
| rs538260154 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708949 | TGCCTTCTTTCAGTC[-/T]TTTTTTTTCTTTCCT | 27342 |
| rs538284576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726261 | GTGCCTCCAGTTCTG[C/T]AGTCCTCTCTTCCTG | 27342 |
| rs538286059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710275 | ACAATTTTTTAATCC[A/G]TTCATCTTGTTGATG | 27342 |
| rs538294382 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717179 | TCAATTGATTATTTT[A/C]TTATATCTCTTTGTG | 27342 |
| rs538308413 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681541 | GTAGTTGGGACCACA[C/G]GTGCCCGCCATCATG | 27342 |
| rs538319690 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732296 | GCCTCATTGAGCAGG[C/G]GGTGCGAGGCCTCTG | 27342 |
| rs538328026 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767550 | GGTCTGAATCTTTGT[C/G]TGTCCCCCAAATTCA | 27342 |
| rs538329261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805905 | ATGCACCATCACACC[A/G]GGCCAATTTTTTTTT | 27342 |
| rs538336677 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737842 | CAGCCTGCTACTGCT[A/G]AACAGGTTAGCGGTG | 27342 |
| rs538365792 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701398 | CCCCAGCTACTAGGG[A/T]GGCTGAGATGGGAGG | 27342 |
| rs538391682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767094 | TGCAACCTCCATCTC[C/T]CCGGTTCATGCGATT | 27342 |
| rs538394022 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681072 | TGGGTGACAGAGCGC[C/G]ACTGTCTCAAAAAAG | 27342 |
| rs538395872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66685302 | GGGAATATAGGCACT[C/T]GCCACCATGCCCAGC | 27342 |
| rs538412508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772646 | GGGCGCAGTGGCTCA[C/T]GCCTGTAATCCTAGC | 27342 |
| rs538483084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737467 | CAGTCTAAAACAATA[C/T]GGAGAGTACCTTTAG | 27342 |
| rs538497147 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737048 | TTATATATATATGAG[A/G]GGGGAGAGAGAGAGA | 27342 |
| rs538518050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735621 | TTCCCCTTTGGTGCT[A/G]TTCTCGTGATGGTGA | 27342 |
| rs538547730 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747802 | TTCTTATTGTGCTAT[A/G]ATTTTTTTCAGTGGA | 27342 |
| rs538555372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742171 | AAAAACTAAGAGTCT[A/G]TTCCTTAAAATTGTT | 27342 |
| rs538558832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697709 | CAGACTGTGTTCTCC[A/G]GCCTCAGCGAGGTGG | 27342 |
| rs538580789 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66740865 | GCGGCGGGGCGTCTC[C/G]GGCTGGGGGTGGCAG | 27342 |
| rs538589516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778353 | TTTAGAGTTGGATAC[A/G]CCTTCAGAGAAAGTA | 27342 |
| rs538611933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725310 | AATTTTACAATATTT[C/T]CCTTATCCCTAAAAG | 27342 |
| rs538648162 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731701 | CAGCCTGGGTGACAG[A/G]GAGCGAGACCTTGTC | 27342 |
| rs538665529 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752748 | GGGGTGGGACCCAGT[A/G]CTCTGTGTTTTAACT | 27342 |
| rs538696457 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724651 | GCGTGAGCCACTGCA[C/G/T]CTGGCCTGAATCAAT | 27342 |
| rs538704490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716706 | TTGGTGTGAATAGAC[C/T]ATTTACATTCATTGT | 27342 |
| rs538715495 | snp | A/G | 0.0876345 | 0.190099 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723815 | GAACTCCTGACCTCA[A/G]GTGATCTGCCCACCT | 27342 |
| rs538725847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752329 | GTGAAACCCTGTCTC[C/T]ACTAAAAATACAAAA | 27342 |
| rs538735260 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730949 | AACTGGCAGGGGTGG[C/G]GTGGATTCGGGGAGA | 27342 |
| rs538788761 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742498 | GGAAGGGATCAGGGA[A/G]TACTTTCTGCATGTG | 27342 |
| rs538796543 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767765 | AACCACCAGACACCA[A/T]CATCTGTTGACTTCC | 27342 |
| rs538797315 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745769 | TGAGACTCTATCTCA[-/A]AAAAAAAAAAAAAAA | 27342 |
| rs538832775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736928 | TGCACAGACACCTAC[A/G]TATACAGACACACAC | 27342 |
| rs538883286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786464 | ACTGGAGCACAATAG[C/T]GCAGTTGCTGCTCAC | 27342 |
| rs538900232 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693955 | TGGGATTACAAGAAC[A/G]TTCCACTACGTTTGG | 27342 |
| rs538926314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692390 | CTACAGCATTGTCTT[A/G]AGGTAAGAAGAACCT | 27342 |
| rs538959887 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735014 | CGTTAAGGAAGTTAA[G/T]GAAAATTTATGAATG | 27342 |
| rs538964444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705123 | AAGCAATAGATGGCC[A/G]GGCGCGGTGGCTCAT | 27342 |
| rs538985597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760031 | ACACCCTTATCATAT[A/G]GAGCATAGGGCTAGT | 27342 |
| rs539001722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687977 | GTAATCCCAGCTACA[C/T]GGTAGGCTGAGGCAG | 27342 |
| rs539019071 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66682095 | CCGTGCGTTACGGGC[G/T]TGCGCTGGCGGTGCC | 27342 |
| rs539055556 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695078 | GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC | 27342 |
| rs539067045 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690957 | TTAGCCGAGTGTGGT[A/G]GGGAGCGCCTATAAT | 27342 |
| rs539075806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781524 | CCCCTTGTCCCCCAC[C/T]ACCCAATAGGCCACG | 27342 |
| rs539084457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743565 | GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC | 27342 |
| rs539087572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694456 | TCTGGCTGGAAAGGT[A/G]GGAAAGGACCAGGCC | 27342 |
| rs539101867 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711064 | ACTCAGGAGGCTGAG[A/G]TGGAAGGATCACTTG | 27342 |
| rs539136488 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700953 | TGGCAGAGAGCCATT[A/G]TGAGTCAGTTCAGTG | 27342 |
| rs539156881 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762485 | GTCCCAGCTACTCAA[G/T]AGGCTGAGACGAGAG | 27342 |
| rs539158824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748540 | AGTCTGACAAGGGCA[C/T]ATATTTGTTTGTTTG | 27342 |
| rs539163834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780414 | ACAACCTGATAGACT[C/T]GTGAGGATTATACAA | 27342 |
| rs539195227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788160 | GTGCTTTTTAATAAA[C/T]TTGGGGCTGGGCGAG | 27342 |
| rs539252524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698419 | GAGAGTCAGAGGAGA[A/G]TGCAAGGTCCCCACC | 27342 |
| rs539260078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736419 | GGGCCATTTAACTTG[C/T]CCTATAGACAGAAGA | 27342 |
| rs539295543 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712580 | GGCTGAAGGGATCCT[C/T]GCACCTCAGCCTCCT | 27342 |
| rs539331616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718763 | TTCTCAAAGCCTGTG[C/T]TGTTTAGGATCAAAT | 27342 |
| rs539332656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711796 | TTTCACCATGTTAGC[C/T]AGGATGGTCTTGATC | 27342 |
| rs539339688 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754220 | TGTTAGCCAGGACAG[C/T]CTCGATCTCCTGACC | 27342 |
| rs539356694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66753325 | ATTTGTAAAGAACAG[A/G]TGTTGCTGTGAACCC | 27342 |
| rs539356742 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746727 | CTCCCCGGTTCAAGC[A/G]ATTCTTGTGCCTCAG | 27342 |
| rs539357875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760325 | AAACTCAACATGTTG[C/T]TCTTGTGTTAATAGT | 27342 |
| rs539433261 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701106 | CTGTTTGTGAGCAGC[C/T]GTGTGGCAGGTATGA | 27342 |
| rs539436031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789510 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAAAT | 27342 |
| rs539442481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788714 | CTGGGCACAGTGGCT[C/T]ACGCTTGTAATCCTA | 27342 |
| rs539446294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796354 | ATCTCCATTTGTATA[C/T]CTCAGAGAGCTCTAC | 27342 |
| rs539481065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777384 | CTAATTCCTGGGTCA[A/G]TATTTTTCCATTATA | 27342 |
| rs539501584 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718064 | CCCTTAGAAAACTAG[G/T]TAAATAGGTAGGCCA | 27342 |
| rs539554865 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66755864 | ACTCTACATTGTATT[A/C]CAGGGAGTTGATTAT | 27342 |
| rs539557062 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706962 | AATTTTTTTTTGGTA[G/T]TTTTAGTAGAGACGG | 27342 |
| rs539563058 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785451 | TGGCCTTTGTCTGCA[A/G]GTTAATGTCCTTTCA | 27342 |
| rs539567161 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749749 | GGCCAAGGCGGGCGG[A/G]TCACGAGGTCAGGAG | 27342 |
| rs539572483 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713218 | GCGATCTCAGCTCAC[C/T]GCAAGCTCTGCTTCC | 27342 |
| rs539591371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684044 | CCCGAGCCTGGAGGG[C/T]GGTTATTAAAGAGAA | 27342 |
| rs539595819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706503 | CACCCTTTGCCTCCC[A/G]GGTTCAAGCGATTCT | 27342 |
| rs539607407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | RABGEF1 | GRCh38.p7 | 7:66768886 | CACCACTGCCTGCAC[A/G]TTTGAGACCAAGGAT | 27342 |
| rs539609815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761932 | GGCAGGCACCTATAG[C/T]ACCAGTTACTTGGGA | 27342 |
| rs539623964 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801952 | TCTCTCTGTCACCCA[A/G]GCTGGAGTGCAAGTG | 27342 |
| rs539643563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794586 | AAATTATCAAGCCCA[A/G]TGTTGTAAGGGCCAT | 27342 |
| rs539653792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801059 | TGCATAAAATTTTGA[A/G]AGTCATCAAGTCCTC | 27342 |
| rs539655873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793875 | GTATCGGCCCTTGGC[A/G]TGTGAGGTCAGTGGC | 27342 |
| rs539660263 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719450 | CCTCAAGCACCTCGG[C/T]CCCCCGCAGTGTGCT | 27342 |
| rs539670802 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768334 | CACCAGTGTATATAT[A/C]TTCTTTGTTAAAGTG | 27342 |
| rs539674570 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803655 | CAGCATTTTGGGAGG[C/T]TGAGGTGGGCGGATC | 27342 |
| rs539684493 | snp | C/T | 4.97806e-05 | 0.00498877 | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66809230 | TATTGACTCTGAAAA[C/T]GTTGAAAATGATAAA | 27342 |
| rs539697026 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795211 | CCCCTTTTCTTCCTT[C/T]TCACCTAATAAAACC | 27342 |
| rs539768612 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765709 | GCTCCATCATTCAAG[A/G]GAACAGCCCCGACTT | 27342 |
| rs539783155 | snp | A/G | 0.000139373 | 0.00834667 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775208 | ATCTAGGTCATTCTA[A/G]TCCTCTCTTGAATTG | 27342 |
| rs539790860 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682504 | TGCCGGCATCTCCAG[C/G]GCCCGGCCGTGCCCC | 27342 |
| rs539817263 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708276 | GCCATGTAGTTTGGG[G/T]TTTTTTTTTTTCCTA | 27342 |
| rs539829802 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694167 | AGAGAGCAGAAGGAT[C/T]AGGCACATCCTTGCT | 27342 |
| rs539831628 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686973 | AGTACAGGCACCCAC[C/T]ACCACGCCTGGCAAA | 27342 |
| rs539860024 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780043 | TTACATTTTAAAAGG[G/T]TTTTTTTTGTTTTAA | 27342 |
| rs539870246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693758 | CTCAGGGAATCATTC[A/G]TTCATTATTCATGCA | 27342 |
| rs539921921 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786868 | TTGCAAATGAGACGG[A/G]CAGCTATGTCATTAA | 27342 |
| rs539922223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762699 | AGGTGGTAAGAACAC[A/G]CCTCTACCCTCTCCT | 27342 |
| rs539963922 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741785 | GATCCTCCCGCCTCG[G/T]CCTCCCAGAGTGTTG | 27342 |
| rs539964196 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698667 | GTGATCCCCTGTGAA[A/C]ATGCATTGTCCCCCT | 27342 |
| rs539967875 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750801 | TGATTCTGCCATTTA[C/T]GTCAGTGAAATGCAA | 27342 |
| rs539969107 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779533 | AAAAATTAAAAAATT[A/T]GCTGGGCTAGTGCCT | 27342 |
| rs539988880 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698404 | GGGCAGCCCACGAAA[C/G]AGAGTCAGAGGAGAG | 27342 |
| rs539999577 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720354 | AGGCATGCACCACCA[C/T]GCCCAACTAATTTTT | 27342 |
| rs539999868 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727686 | CCAGGCTTCTCCAGG[C/T]CAGCCCCTCGCAGGG | 27342 |
| rs540004485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705323 | AAAAATGAAATCCCA[C/T]CTACTAGGGAGGCTG | 27342 |
| rs540033607 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786146 | TCCCACATCATTTCT[A/G]TTTTCTCCAAGCCCT | 27342 |
| rs540062742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792897 | ATAAGCAGATCTGTA[A/G]CATAGTGTTAAGTCC | 27342 |
| rs540121491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752962 | ACCTAGAAAACATCT[A/G]TTGAGCACCTCCTCA | 27342 |
| rs540125942 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720862 | AGTGTCAATTGAATT[A/T]CCATATGCTAGCTCA | 27342 |
| rs540130304 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695567 | GACTGGGGACAAAAG[C/G]CAGGCTGGAGAGAGT | 27342 |
| rs540162572 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743037 | CTCTCTGGCCAGGCG[C/T]GGTGGCTCACGCCTG | 27342 |
| rs540206274 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707670 | TCCAGACTGGGCAAA[A/G]GAGCAAGACTCCATC | 27342 |
| rs540217441 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699976 | TGTGGGCACAGTTAT[C/G]TTCATCCTCTCCGGG | 27342 |
| rs540244037 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731520 | ACTAGGAGTTGAGAC[C/T]AGCCTGGGCAACATG | 27342 |
| rs540244226 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706160 | ACCCGCCTCGGCCTC[A/C/G]CAAAGTCCTGGGATT | 27342 |
| rs540247860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730589 | TTGGTGGCAGGGTCT[C/T]ACTGTGTCACCCAGG | 27342 |
| rs540266610 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737062 | GGGGGGAGAGAGAGA[A/G]AGAGAGAGAGTGAGA | 27342 |
| rs540277899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787777 | ACAGAGCTTCATGTG[A/G]TGAGGGCAATTTTAA | 27342 |
| rs540283203 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788754 | GAAGCCAATGCGGGT[G/T]GATCACCTGGCCAAC | 27342 |
| rs540294677 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742854 | TCAAGCAATCTTCCT[G/T]CCTCAAGCGTCCCAA | 27342 |
| rs540320310 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742329 | ATTTTTAATGACCTT[C/G]CAAGCAGTCATGTTT | 27342 |
| rs540327794 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729140 | TATTTTTAGTAGATA[-/T]GGGGTTTCACTGTGT | 27342 |
| rs540329634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736635 | GAGGGTGAGGCAGGT[A/G]GATCACTTGAGGCCA | 27342 |
| rs540390846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712250 | TCATTTATTTAGGTC[C/T]TTCTAGATTCCTTTT | 27342 |
| rs540413294 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800675 | TTGTGTTTTTCCTGA[C/G/T]TCTTACTAGAAAGTT | 27342 |
| rs540424952 | in-del | -/AAACA/AAACAAAACA | 0.00438556 | 0.0466571 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684442 | GCAAGACTTCGTCTC[-/AAACA/AAACAAAACA]AAACAAAACAAAACA | 27342 |
| rs540459023 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704762 | TTTGCAGTGAGCCGA[A/G]ATTGTGCCACTGCAC | 27342 |
| rs540469137 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689137 | AAAGCTCTCAAATCA[A/G]TCACCTAACTATACA | 27342 |
| rs540470001 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718452 | AATTATCTTTTTCCA[G/T]GTAAGATGTTTAGAT | 27342 |
| rs540474939 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800248 | CAGAAGAAATGGAGG[G/T]TTGCTTAAGGTATTA | 27342 |
| rs540476325 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711366 | GTTTTCTTCTTAAAG[G/T]TTTAGTCTTACATTT | 27342 |
| rs540506208 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746207 | GCTTTAGGAAAACAT[A/T]ATACTTTTATGGTGC | 27342 |
| rs540515061 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710387 | CATGCTTTCATTTTT[A/C]TTCAGTAAATAACCC | 27342 |
| rs540556926 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707438 | TGGCTCACACCTGCA[A/G]TCCCAGCACTTTGAG | 27342 |
| rs540604770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748823 | TCCATTTCTCCAATT[C/T]GAACTTTCTGATTAG | 27342 |
| rs540617632 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788290 | TCTCTACTAAAAATA[C/G]AAAAATTAGCTGGGC | 27342 |
| rs540636554 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692929 | GCTGAGGCAAGGATC[A/C]TGGGAGTTTCAGGTA | 27342 |
| rs540713183 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727535 | CCTGCCAAGCCAGTG[A/T]CCTGGGTGGACCCAG | 27342 |
| rs540734372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754538 | CACGTGAGCCCAGGA[A/G]TTGGAGACCAGCCTG | 27342 |
| rs540758239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719900 | TGACTTTACAGAACA[A/G]GGTTTGCTGGTCCCT | 27342 |
| rs540785946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719084 | CGCAGAGCATTTGGT[A/G]GTTACCCAACTGCTT | 27342 |
| rs540786341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760632 | TATTTTTAATAGAGA[C/T]GGAGTTTCACTGTGT | 27342 |
| rs540794271 | in-del | -/AG/AGAC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705443 | TCCATCTCGAAAGAA[-/AG/AGAC]AGAGAGAGAGAGAGA | 27342 |
| rs540807727 | snp | A/G | | | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760882 | CATCCTCCCACCTTC[A/G]CCTCCCAAAGTGCTG | 27342 |
| rs540823099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725589 | GAGTTCGTGAATATT[A/G]TGATGTTATGCTGTT | 27342 |
| rs540823483 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767991 | CTGTTGTATGGGTGC[A/C]CCATAGTTTGTTTAT | 27342 |
| rs540900588 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767134 | CAGCCTCCCAAGTAG[C/G]TGGGATTACAGACGT | 27342 |
| rs540908119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760167 | TTAACTGCTTACACC[A/G]TTTTCCTTCCCCTCC | 27342 |
| rs540912765 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770398 | TAGCGATTTACCATA[C/T]AGCTGTGAGACTGAA | 27342 |
| rs540932322 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783286 | TTTAACATGTCAGTG[C/T]TTCTATTGATTGTTA | 27342 |
| rs540933816 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702122 | TATGGATTTGCCTAT[A/T]TGGATATTCATATTA | 27342 |
| rs540955069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731208 | TCCAGGCCTGGCAAC[A/G]GGACTTGGCAGAATG | 27342 |
| rs540969174 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762944 | ATAGCATGTGCAAAG[G/T]CTCTCCCAACAAAGG | 27342 |
| rs540979201 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770833 | GGGTGTAAAGTGATA[C/T]CTCATTGTGATTTTG | 27342 |
| rs540984771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694707 | GAGAATGAAGTCGGA[A/G]TCTCGTGGATTGGCC | 27342 |
| rs541014660 | snp | C/T | 4.94214e-05 | 0.00497074 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66795567 | CTACCACAATGTGGC[C/T]GAAAGGATGCAAACT | 27342 |
| rs541022399 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684687 | TCAGCCAGGCTGGAG[A/T]GCAGTGGCCTGATCT | 27342 |
| rs541025115 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720480 | TAGGATTACAGGCAC[C/G]AGCTACTGTGCCCAC | 27342 |
| rs541040511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769731 | AAGATAGAGATCTTA[C/T]CATGCTTTCCCCTTT | 27342 |
| rs541066351 | in-del | -/A | 0.151001 | 0.229563 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723710 | CTCAGCCTCCTGAGT[-/A]GCTGGGATTACAGGG | 27342 |
| rs541082357 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | RABGEF1 | GRCh38.p7 | 7:66809463 | TAGTTAATAATAAAA[A/T]ACTACTTATTTGAGT | 27342 |
| rs541097101 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696837 | CCATCTGGTGGATGG[C/T]TTCTGAATAAGCAAG | 27342 |
| rs541100411 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683841 | AACTGCCTGGGCTCA[A/G]GTGAACCTCCCACCT | 27342 |
| rs541117636 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740358 | TCGGCGCAGTAGCTC[C/T]GCTCCACCTCCCATT | 27342 |
| rs541155181 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776265 | GTCTCCCCTGAAGGC[C/T]GGGGAATGAATAATA | 27342 |
| rs541164235 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768411 | TGACATCTGAGTTTT[C/G]AGAGTTCTTTATACA | 27342 |
| rs541197091 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725122 | TTCTGGGTCTGTTTC[C/G]ATTATTATTTTTTTA | 27342 |
| rs541199693 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715082 | CCTTCTCTTTCTCTT[A/T]CTCCTCCTTCTCCTC | 27342 |
| rs541202001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784090 | AAGCCACTTGAATTA[C/T]GTGCTTTAGTAACAG | 27342 |
| rs541276541 | in-del | -/AAAT | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66809611 | TTTAAAGGATTAAAC[-/AAAT]GAATGCTACAAAGTG | 27342 |
| rs541305071 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701539 | TTGAGACAGAGTTTC[A/G]CCCTTCTTGCCCAGG | 27342 |
| rs541318560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738352 | CTTCACAAAGAAACT[C/T]TGAAATGATATTCAG | 27342 |
| rs541327124 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749742 | TTTGGGAGGCCAAGG[C/T]GGGCGGATCACGAGG | 27342 |
| rs541328957 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743260 | GGTTGTGGTGAGCCA[A/G]GATTGTACCAATGCA | 27342 |
| rs541331098 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700808 | TGGCCCGAGGCCTGG[A/G]CACTCTCTGAGGACA | 27342 |
| rs541350535 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743968 | TCTTACACACAGGCT[G/T]CTATGTAGCTGATAA | 27342 |
| rs541381823 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761459 | TTGCAAAGGATCCAG[G/T]TAAAGGAGATGCTGG | 27342 |
| rs541444046 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691203 | ACCACACTGACAGAC[A/C/G]GTTTGACAGTTTCTT | 27342 |
| rs541444207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801507 | CTAACTTTTCTGGTA[C/T]CCCTTGGCCATCCCC | 27342 |
| rs541467205 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779742 | CACTTGCTGTTTGAG[C/T]CCTAGCCAAAATTAT | 27342 |
| rs541528614 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777773 | ACTCCAGCCTAGGCA[G/T]CAGAGTGAGACACCA | 27342 |
| rs541544000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738298 | TGCTGGGATTACAGG[C/T]GTGAGCCACCATGCC | 27342 |
| rs541554576 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725908 | CAATCAGAGGGGGAA[A/G]CTGTGACCCTTTCTT | 27342 |
| rs541556239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767364 | GAGTATAATGGTCTG[C/T]GAATTTTTAAATTTT | 27342 |
| rs541594185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702126 | GATTTGCCTATTTGG[A/G]TATTCATATTAATAG | 27342 |
| rs541636009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744270 | TGAAATGGTGGCTCA[C/T]GCCTGTAATCCTCGC | 27342 |
| rs541655454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774323 | CTACCCTTCAAGTTG[C/T]TCACACAGCTACCTG | 27342 |
| rs541655718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737690 | CGTGGAAAAACACAT[C/T]CTCAACAACAGCAAA | 27342 |
| rs541708321 | in-del | -/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735596 | TGACAGGATCATTGT[-/G]GGGGGGGGTTTCCCC | 27342 |
| rs541721095 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795996 | ATACAAAAAGTAGCC[G/T]GGTGTTGTGGTGCAC | 27342 |
| rs541725335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707820 | AGGCTTACAAATGTT[A/G]TATCTTCTTGAAGGA | 27342 |
| rs541730607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742493 | AGCCTGGAAGGGATC[A/G]GGGAATACTTTCTGC | 27342 |
| rs541813198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719825 | TGTTTTCCTGTTACA[A/G]TAGTAGGGTTGAGTA | 27342 |
| rs541820576 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696260 | TGTAGAGACTGGGTT[A/T]TACCATGTTGCCCAG | 27342 |
| rs541828646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783289 | AACATGTCAGTGCTT[C/T]TATTGATTGTTATTC | 27342 |
| rs541828924 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745459 | TGAGTGGCTTCTTAG[A/C]CCATCAGTAAAGTTA | 27342 |
| rs541829169 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767946 | TTGGGTGTACTGATA[A/C]CTGTTGTTGTTGTTT | 27342 |
| rs541857227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695902 | ATCTGGGAGTCGGAG[A/G]TTGCAGTGAGCTGAG | 27342 |
| rs541866679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775584 | GGTTGAAAGACATTG[C/T]GTTTTAGAGAAATTT | 27342 |
| rs541878446 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769485 | GCTTCCACTCTGATC[A/G]GCAGAGCATGTGCAT | 27342 |
| rs541887985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789640 | GTGAGCCTAGATCAC[A/G]CCACTGCACTCCAGC | 27342 |
| rs541892746 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736605 | GGTTAGAATGGGTAG[G/T]ACTTGGCAGGTGATG | 27342 |
| rs541893048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808775 | TTCATGAGTTTGTTT[C/T]GTTTACTTTAGCTTC | 27342 |
| rs541893339 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702116 | TGTCTATATGGATTT[C/G]CCTATTTGGATATTC | 27342 |
| rs541902592 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732501 | AGGTCCATATACCCA[A/G]GTATCTCCCACTGGG | 27342 |
| rs541940067 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766968 | GTTCTGTACTTCTCC[C/G]TAATCCAACCTGGAA | 27342 |
| rs541956484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695180 | AGCCGGGCACGGTGG[C/T]GTGCACCAGTAATCC | 27342 |
| rs542098564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66755916 | GCTAACGTTTGGACA[A/G]ATAATGTTTTGTTAT | 27342 |
| rs542101659 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752274 | CGAGGTGGACGGATC[A/G]CAACAAGGTCAGGAG | 27342 |
| rs542111835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787588 | AGCCTCACATGATCC[A/G]CCCACCTTGGCCTCC | 27342 |
| rs542115495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748078 | TAATCAGTTACATGG[A/G]TCAGTGACCATACGA | 27342 |
| rs542128362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794991 | AGCAAAAAGAATGAG[A/G]TGGTCATGGTGAGAC | 27342 |
| rs542131586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706630 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTGA | 27342 |
| rs542165486 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755241 | GGAGCTTGCAGTGAG[C/G]TGAGATTGCATCACT | 27342 |
| rs542167051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699399 | GTTTTCTCATCTGTA[A/G]AATGGGAGTGGCTGG | 27342 |
| rs542201056 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776131 | GGTACTCAGAGTTAT[C/G]CAGTCAAAGCGAAAT | 27342 |
| rs542254700 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709056 | GAGTTTCACTCATGT[C/T]GCCCAGGCTAGAGCG | 27342 |
| rs542266113 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797792 | CTGTGTTCTTGGTCC[A/G]TTACCATCTCCTCAA | 27342 |
| rs542316666 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743918 | TTACAAACATGAGCC[A/G]CTGCACCCGGCCCTA | 27342 |
| rs542332992 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694844 | CAATGAGGGGAACAA[C/T]GGGGCTGGGGGATCA | 27342 |
| rs542336959 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798100 | CCAGCCTGGGCAACA[-/G]AGCAAGACTCCTTCT | 27342 |
| rs542337878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719268 | CAGTCTGAACCACAA[A/G]TGGAGAGCTTCTCTT | 27342 |
| rs542339903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739283 | CTGTTGTACCCTCAG[C/T]GTAGCACACATTAGG | 27342 |
| rs542388425 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732128 | CTAGAACGCCCGGCT[C/G]ACCAGGCCACCGCCC | 27342 |
| rs542410673 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713291 | GGACTACAGGTGCCC[A/G]CCACCATGCCCAGCT | 27342 |
| rs542451551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795422 | TTACTACCAGTACAA[A/G]GAATGGCTTTTGGAA | 27342 |
| rs542463634 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802005 | GCCTTGACCTCACAG[G/T]CTCAAGCGATCCGTC | 27342 |
| rs542478637 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770693 | CTTGCTGTGTTGCCC[A/G]GGCTGGTCCTGAACT | 27342 |
| rs542519840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713364 | CAATCTCCTGACCTC[A/G]TGATCGGCCCGCCTT | 27342 |
| rs542556114 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | RABGEF1 | GRCh38.p7 | 7:66809358 | TCAACTGATTGGGAT[C/T]TAGAATGTAACTAAA | 27342 |
| rs542610652 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689477 | CTAGAAACACAAAAC[C/T]TACCAAGACTAAATC | 27342 |
| rs542615305 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790417 | TATCTCACACATGAA[A/C]ACCCAGCGTGAAAAC | 27342 |
| rs542632349 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681363 | CTTTGTGACACTGGT[G/T]AATTATTTCACTTCT | 27342 |
| rs542639231 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784304 | ACAATGAAAGGGACT[G/T]TAGCAACTATGGAGT | 27342 |
| rs542676594 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768274 | AATATACAAACATCC[-/T]TGACTGCACAGTATG | 27342 |
| rs542678911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796738 | TGGGATTACAGGTGC[A/G]TGCCACCACACCCAG | 27342 |
| rs542787625 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772186 | AGCTATCAGCAAGTC[A/C]GTTTAATATTAAGGA | 27342 |
| rs542788806 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776975 | CCGAGTCCTGTCCAC[A/G]CTGAGGGACAATAAT | 27342 |
| rs542814845 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777894 | CTCCCCTCATCCCCC[A/G]TCTTTTTGAATGATA | 27342 |
| rs542845843 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66753201 | CTAAGTGGGTTCATA[A/C/G]ATAGGATGACCATGT | 27342 |
| rs542870968 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684554 | CTACCACCCAGGCTT[A/G]AGTGATTCTCTTGTC | 27342 |
| rs542879474 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697473 | TGGCTCTGTCTGCCC[A/G]TCCCAGCCGCCAGCT | 27342 |
| rs542897842 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727883 | GCTGCCTTGGAACAC[A/C]CGCGTGGCTGCCTCT | 27342 |
| rs542911551 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740650 | TGACGTTTACGCGCC[A/G]CGCGTAACGTGCGTT | 27342 |
| rs542965662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703619 | ACAATAGATGTATTG[A/G]CTTTTTTTTTCTGGA | 27342 |
| rs543008106 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743035 | GTCTCTCTGGCCAGG[C/T]GCGGTGGCTCACGCC | 27342 |
| rs543011008 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716847 | GCAGTGGTGCAATCT[C/T]GGTTCACCACAAGCT | 27342 |
| rs543012775 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715357 | GCTAATCTTGAACTC[C/T]TAGCCTCAAGCAATC | 27342 |
| rs543016812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757414 | GTTTTATTTTCTTTA[A/G]GCCTTTCAGATACAT | 27342 |
| rs543023011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720926 | ATTATTATTATTATT[A/G]TTGTTATTTGAGACA | 27342 |
| rs543025522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806108 | GGGAATGTACTGTAA[A/G]GCTAATGAATTTGGA | 27342 |
| rs543059696 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760359 | TTCTTTTTAGTGTTC[A/G]GTATTCTCTTGTGTG | 27342 |
| rs543081624 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680841 | AATCCTAGCACTTTG[A/G]AAGGCCAAGGCGGGC | 27342 |
| rs543088242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803502 | GCGGTGCTGTCACCA[C/T]GTGCTTCAGCACCCT | 27342 |
| rs543088695 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805512 | TGTGAGAAGGCAGCA[A/C/T]GGCTGAGGAAGCTCA | 27342 |
| rs543096031 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722859 | GGATTACACTGAATC[C/T]GTACATCATTTTAGG | 27342 |
| rs543134826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729306 | CTCCATCCTCCCCTC[C/T]ATTCTTCGTTCCTCA | 27342 |
| rs543161506 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811694 | AAAAAAGGAGTTAAT[A/G]TAATCAATATAGAGC | 27342 |
| rs543170055 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802239 | GAGTACTACTAACAC[C/G]TAGTGGGTAGAGGCC | 27342 |
| rs543196545 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684395 | GTTGTCTGAACCGAG[G/T]TTGCACCAGTGCACT | 27342 |
| rs543221906 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727568 | TGGGTGGAGAGATGA[C/G]ATGTTTGGTTCTCTG | 27342 |
| rs543228349 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743363 | TCTCTCTCTCCCTGT[C/T]TCCCAGGCTGGAATG | 27342 |
| rs543230913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692643 | TCCAGTTCTAAGTGG[C/T]GGGACTGGGGAGTCA | 27342 |
| rs543233568 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690997 | TTCGGAGGCTGGGGC[A/C/G]TGAGAATCGCCGGAA | 27342 |
| rs543265231 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741738 | GATCTCACAGTGTTG[C/T]CCAGGCAGGTGTGAA | 27342 |
| rs543309621 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764434 | TTCATTTGATAAGGT[C/G]CTCTGAAGCACAAAC | 27342 |
| rs543314236 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799239 | TCAGTGATGCCTCAG[A/G]CTTTCCCTAAACTGA | 27342 |
| rs543318320 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697029 | GCAGAAGGAGGCACC[C/T]CTGACCCCATGCCCC | 27342 |
| rs543319630 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695804 | AACCCTGTCTTTACT[A/G]AAAATACAAAAATTA | 27342 |
| rs543372696 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764476 | GTTGGAGTACAATTT[A/T]TCTGTCTTTTGTTGC | 27342 |
| rs543373621 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750590 | TCAATGCATTAAAAG[A/T]TACATATTTTTCTAG | 27342 |
| rs543375146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785000 | CACATGAAATGTTCA[C/T]GGGATAGCTATATTA | 27342 |
| rs543431785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66685591 | TGTAAACAGGAATTC[C/T]GCACTCATTTCTGTT | 27342 |
| rs543455392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714791 | ATACAAAAAATTAGC[C/T]GGGCATGGTGGCTGG | 27342 |
| rs543455731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802950 | TTAAATAAAAGAGAG[A/G]AAAAAAAATCACCAA | 27342 |
| rs543462010 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729172 | AGCCAGGATTGTCTC[A/G]ATCTCCTGACCTCAG | 27342 |
| rs543483537 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756513 | AAAGATTTATAAATT[G/T]TGTTAGTACTATTTC | 27342 |
| rs543506730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735216 | GTAGTGCTTGTGTTA[C/T]CATGGCTTGCATTTT | 27342 |
| rs543523055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692465 | GGGTGGCTCCAAGGC[A/G]CAGTGGCCCTGCCAG | 27342 |
| rs543527805 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740618 | TTCCTCCCGTCCAGA[A/G]TCAAAGGCCCCGGAA | 27342 |
| rs543575416 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694634 | AGCTAGTGACGTGGA[C/T]GTCACGATACCCCGG | 27342 |
| rs543583966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683900 | TGGGTGCCGCCACAC[C/T]CAGCTGATTTTTAAA | 27342 |
| rs543601408 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762362 | TTGGGAGGCCAAGGT[C/G]GGTGGATCACTTGAG | 27342 |
| rs543638181 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740418 | AGTCGCCGCGGAGCC[A/G]GCGTCGCCCTCCAGC | 27342 |
| rs543643284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784718 | TTTAGATATTGAATT[C/T]AGTTTGTAAAGGAGA | 27342 |
| rs543671209 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689967 | TTTTGCAAACTCTTT[C/G]AAAAACTTGAAGAGG | 27342 |
| rs543697260 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733005 | CTTTAGCCTGACGCC[C/G]TTCCCCAGCTCCCTA | 27342 |
| rs543700271 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744860 | TGATAAGAATAACTC[A/G]TTGATTTCTTTGATT | 27342 |
| rs543710793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744296 | CTCGCACTTTGGGAG[A/G]CCAAAGTGGGAGGAT | 27342 |
| rs543788311 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713375 | CCTCGTGATCGGCCC[A/G]CCTTGGCCCTCCAAA | 27342 |
| rs543801748 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693120 | GCGGGCTTCTTCATG[G/T]ACAGAGCATTTGGCA | 27342 |
| rs543807385 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722806 | AATTTTAGAATCAGC[A/G]TGTCACTTTCTACAA | 27342 |
| rs543807918 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786035 | TGCCCAGTCAGCCTT[A/G]CCATAAATGGATAAT | 27342 |
| rs543816556 | in-del | -/A | 0.26675 | 0.249438 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699692 | CAAAATTCCATCTCA[-/A]AAAAAAAAAAACAAA | 27342 |
| rs543849417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781521 | CCTCCCCTTGTCCCC[C/T]ACCACCCAATAGGCC | 27342 |
| rs543855180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806892 | CAAGCAATCCACCCA[C/T]CTCAGTTTCCCACAG | 27342 |
| rs543863562 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811633 | TCAACCTTGTTCTTG[C/G]AGTTCTACCAAGGTA | 27342 |
| rs543870201 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792778 | CATTTATTCATTCAA[C/G]CCATACTGAGCACTA | 27342 |
| rs543871326 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759052 | GTGCAATGTATGTGT[A/G]TAGTGTCATGCACAT | 27342 |
| rs543906108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692023 | GATGGTGCCACTGCA[C/T]TCCAGCTTGAGCGAC | 27342 |
| rs543928646 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734643 | GAGCCATGTTGGCCA[A/G]GCTGGTCTCGAACTC | 27342 |
| rs543942807 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697442 | ATGGGTCAAACCGAC[A/G]TCTCTCCCTTCACAG | 27342 |
| rs543973259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768064 | ATCACAAATATTGCT[A/G]CTATAACCGTTTGCG | 27342 |
| rs543982432 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769853 | AGTTTACCTTCTGTC[C/T]GTGCTACATCATTCA | 27342 |
| rs543994182 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777134 | AGAATTATCTTGCAG[A/G]GAGCACAAGGGCATT | 27342 |
| rs543999900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704614 | AGGAGATCGAGACCA[C/T]CCTGGCTAACACTGT | 27342 |
| rs544034469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710313 | AGGTTGTTTTTTAGC[A/G]TTTAGCTTTTACCAG | 27342 |
| rs544120159 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798475 | GGCTGAAGATGTGGA[G/T]CCCAAGGTCAGGAGC | 27342 |
| rs544133985 | snp | C/T | 0.000645861 | 0.0179587 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805417 | TAAGTGAGTTCTTGG[C/T]GTTGTGGAGAAGGAC | 27342 |
| rs544203955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778932 | ACCAGCCTGACCAAC[A/G]TGGCACAACCCCGTC | 27342 |
| rs544226298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736090 | AGGAAATGAAAGGGA[C/T]GATGATGGAAAAAAA | 27342 |
| rs544232193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705257 | AATGCAAAAAATTAG[C/T]TGGGTGTGGCAGTGC | 27342 |
| rs544240199 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706317 | AACATATACTTTCAT[A/T]TCTCTTATGCGATAC | 27342 |
| rs544255731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741720 | TTATTTTTTTCGACA[C/T]GGGATCTCACAGTGT | 27342 |
| rs544260013 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750281 | TGGCAAAGTGTTTTC[A/G]TACCCATATGCTAAC | 27342 |
| rs544292164 | snp | C/T | 0 | 0 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772140 | ACATAGTTCTGTCAC[C/T]GTCTAAATACATTTT | 27342 |
| rs544319313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741026 | CTCAGAGTGCGGCCT[C/T]TCCGTCCCAGACGCT | 27342 |
| rs544319399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746822 | AGTGAGACTGAGTTT[C/T]AGCCTTGTTGCCCAG | 27342 |
| rs544326641 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | RABGEF1 | GRCh38.p7 | 7:66712203 | ATCCAACCTGTATCA[A/G]GTCTTCTAATCTGTG | 27342 |
| rs544333122 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800163 | GTGGGTTAACTGATA[A/T]TAGTAGTGTTGGAGG | 27342 |
| rs544361844 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66753841 | TCTCCTGTGTAGCTG[G/T]GACTACAGGCATGCG | 27342 |
| rs544370758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717592 | TGAAACCCCGTCTCT[A/G]GTGTCACCCAGGCTG | 27342 |
| rs544385403 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790779 | GAACTCCTATTCAGG[A/G]ATGTGTTCTCTGATT | 27342 |
| rs544453676 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750351 | GCCCCAGGAAATACA[A/G]TGTTTTATGACAGAG | 27342 |
| rs544453721 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793494 | GATTTTTTATTTTTG[A/G]GTTAGGAATGCTCAA | 27342 |
| rs544499791 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716403 | CCAGGAGTTTGAGAC[C/T]AGCCTGGGCAACGTG | 27342 |
| rs544501680 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723388 | TTATAATGTGAATCT[G/T]TAACTTTTCACAATC | 27342 |
| rs544502038 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681825 | TTCCACCGTGGCCTC[C/G]GCTCCAGGAGTCGCC | 27342 |
| rs544526059 | in-del | -/GAGC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737095 | AGAGAGCGAGAGCGA[-/GAGC]GAGAGAGAGAGAGAG | 27342 |
| rs544543834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758238 | CTGAGACGAAACTGG[C/T]TTGCATCCAGAGCCT | 27342 |
| rs544546442 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728539 | ATTGCCATCACCAGT[A/G]TCTTCACCATTTTTA | 27342 |
| rs544549859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686929 | CGGGTTCAAGCCATT[C/T]TCCTGCCTCAGCCTC | 27342 |
| rs544564534 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754510 | GCACTTTGGAAGGCC[A/G]CAGTGGGCAGATCAC | 27342 |
| rs544596837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736471 | TTTTGGGCAAAGAAT[A/G]CAATGTGAGCAAGAG | 27342 |
| rs544676580 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785653 | GCCGAGGCAGGCGGA[A/T]CACAAGGTCAGGAGA | 27342 |
| rs544690699 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791802 | TTAGAAAAATAAAAC[A/G]ACAACTTTACTCAGA | 27342 |
| rs544766187 | snp | C/T | 0 | 0 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760056 | GCTAGTACAAGACCT[C/T]AGTTTCTAGGAGCTG | 27342 |
| rs544775589 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687528 | AAAGAAGAAGAAGAA[G/T]ATAGGCTATGAGTGG | 27342 |
| rs544778769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759669 | GGGAGCAAAGTGTCT[C/T]CCCTAGTGGGAGCAG | 27342 |
| rs544790133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797858 | ATGTCGGCTGGGCCC[A/G]GTGGCTCATACCTGT | 27342 |
| rs544790169 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680628 | AACGAATCAATTAAT[A/C]TCCACTTTACCAATA | 27342 |
| rs544793889 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767384 | TTTTAAATTTTATTA[C/G]ATTTATGTAAACACC | 27342 |
| rs544797030 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731089 | TTTCAAGGGGGCACA[A/C]AGGGACACTGAGGCC | 27342 |
| rs544797588 | in-del | -/T | 0.0962929 | 0.197165 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746289 | GGATAGGAAGTGTGA[-/T]TTTTTTTTTTTTACT | 27342 |
| rs544817887 | in-del | -/T | 0.491783 | 0.0635686 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767001 | TGCCTGTCAAGTTTC[-/T]TTTTTTTTTTTTTTT | 27342 |
| rs544876573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791978 | TTAGCTGGGCGTGGT[A/G]GCACATGCCTGTAGT | 27342 |
| rs544892091 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66809541 | CTTTTTTCCCTCCAT[C/G]ATTTTCCTATGTGCT | 27342 |
| rs544900030 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695328 | AAAAAAAAAGGACCT[C/T]GAGAAAGGGTCTGAG | 27342 |
| rs544900902 | snp | C/T | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681567 | TCATGCCCGGCTGAT[C/T]TGTAAAATTTCTTTT | 27342 |
| rs544944717 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697561 | AAGTGAGCACTTGGC[A/C]GGCGGGGACCATGAT | 27342 |
| rs544954512 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764389 | CATAAATGACTTGCA[A/G]ATGTTTTCTCTTATT | 27342 |
| rs544962683 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780170 | GGTGTACAGACCTCC[A/G]AAGTCAGAGGAGTTG | 27342 |
| rs544969672 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66753048 | ATTGTAATAGGACAT[G/T]AGTATTATAATGGCT | 27342 |
| rs545055892 | in-del | -/T/TT | 0.36021 | 0.224397 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66685153 | TGCTGGATTATTTGC[-/T/TT]TTTTTTTTTTTTTTT | 27342 |
| rs545060909 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791082 | TTGAAACATTTCTTA[C/T]GCTAAAAATAATTTC | 27342 |
| rs545086514 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724152 | GTTAACAGCTTTTTC[C/G]CCCCAGCACTCTAAA | 27342 |
| rs545114565 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715760 | TATGCTTTTTTTTTT[-/A]AGAGATGGGTCTCGG | 27342 |
| rs545124809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806239 | TTGCCAAAAAAGTCT[C/T]ACAGGTACGTGAATC | 27342 |
| rs545151299 | in-del | -/TTTG | 0.00755907 | 0.0610114 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796582 | TTGGAAGAAGATTTT[-/TTTG]TTTGTTTGTTTGTTT | 27342 |
| rs545171026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730387 | TAAAGGCATCTTAAA[C/T]GGTAGGTTATTATTA | 27342 |
| rs545192020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751282 | GTGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTGT | 27342 |
| rs545207658 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729846 | TGGGACTCTTTCCTT[G/T]CATGGCAATGACAGC | 27342 |
| rs545208963 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765765 | AAAGACTCTAACACA[G/T]TTGGAGGCAATCAGC | 27342 |
| rs545217980 | snp | A/G | | | intron-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811673 | CAAACAGACATAAAA[A/G]TAGAGAAAAAAGGAG | 27342 |
| rs545236034 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715585 | AGGATTATGTAGAAG[G/T]ATGTAGTTAATTTCT | 27342 |
| rs545302895 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693066 | GCTGGTCCCGTGGCC[G/T]TCACTCAGCTGAAAG | 27342 |
| rs545324497 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763640 | AAAAGGAACCCATGC[C/G]CTTTCTCTTATCCCT | 27342 |
| rs545329723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735982 | CTGATAAAACATCAG[C/T]CTTATTATTGAGTAG | 27342 |
| rs545345426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767249 | CTCAGGTGATCCACC[C/T]GCCTCAGCCTCCCAA | 27342 |
| rs545359180 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802466 | CTATTCATGTGAAGG[C/G]AGAGCCCTGGGAGAA | 27342 |
| rs545359335 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737169 | TCCTGGCTTTAGGCA[A/G]TCCTCCCACCTTGAC | 27342 |
| rs545395977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697817 | ACTCAGCAGAACTGC[A/G]GTGGGGCCATCGGAG | 27342 |
| rs545396383 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792974 | TTTTACATTATGAAA[A/G]CAATACTGTACTGGA | 27342 |
| rs545396941 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776266 | TCTCCCCTGAAGGCC[A/G]GGGAATGAATAATAA | 27342 |
| rs545453546 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755168 | GCGTGGTGGCAGGTG[A/C]CTGTAGTCCCAGCTC | 27342 |
| rs545469433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716923 | AGCTGGCACTACAGG[C/T]GACCACTGCCATACC | 27342 |
| rs545485488 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796981 | TCTAGTAAATTAGTT[G/T]TTTGCTGTGTAGACA | 27342 |
| rs545499364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805596 | ACTTGATCAGAGATT[A/G]TGTTTATCCTACGGA | 27342 |
| rs545508599 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742748 | AGTAGCTAAGACTGC[A/G]GATGCGTGCCACCAC | 27342 |
| rs545512437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687851 | AGCACTCTGGGAGGC[C/T]GAGGCGGGCAGATCC | 27342 |
| rs545522838 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787186 | CATGTGCCACCATGC[C/G]CAGATAATTTTTACT | 27342 |
| rs545523427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686842 | TCTTTTTTTTTTTGA[A/G]ATGGAGTCTTCCCCT | 27342 |
| rs545536437 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765251 | CCAGTACGTGGCAGA[G/T]CTGGGGTTGGAGTGC | 27342 |
| rs545567902 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726160 | AGCACCCAGCCTGGG[A/C]TTTGCCCACAGCTGG | 27342 |
| rs545575146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693580 | CCTCACCCACCCTGC[C/T]CTCTCCCATGGAGTT | 27342 |
| rs545613461 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686231 | GGTTGCAATGAGCCG[A/C]GATTGTGCCACTGCA | 27342 |
| rs545630045 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772319 | TTAGTTTTAGTTCTC[A/C]AATGTAGACAATAAG | 27342 |
| rs545679882 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780096 | AGTATGTGTGGGAGG[A/G]AGGCATGTTGTAAGC | 27342 |
| rs545680111 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786829 | ACAGTACTTCTATAC[A/T]TTCTTTAAAACAAGA | 27342 |
| rs545695667 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777620 | AATGCAGAGTCTGTA[A/C]TTTAAAAAGAAACAT | 27342 |
| rs545697009 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747074 | GCTGGGATTACAGGT[G/T]TGAGCTACCGTGCCC | 27342 |
| rs545698115 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735407 | AGTCAAACTGGCAGA[G/T]ATCCACATAAGACCT | 27342 |
| rs545701830 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692698 | CCCGCCTCCCACCTA[A/T]AGCTCCCACCCACCC | 27342 |
| rs545788999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701269 | TTTCAGAGGCTGAGG[C/T]AAGAAGATGGCTTGA | 27342 |
| rs545789257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725615 | CTGTTTTTGTTCCAT[C/T]CATGGCAATTTTATG | 27342 |
| rs545792393 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766637 | TCTCTGTCAAGTCTC[A/G]TTAAATAACTATTAA | 27342 |
| rs545793808 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732040 | CAGTCAGCCGCCTGC[A/G]GGCCAGGGCTGCCAG | 27342 |
| rs545794840 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788909 | GCAGTTAGCCAAGGT[C/T]GCGCCATTGTACTCC | 27342 |
| rs545797355 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755845 | CTCATTCCAGCAGCA[A/G]TCAACTCTACATTGT | 27342 |
| rs545856598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795356 | AAATAATATTAATGG[A/G]TAGGTTTTACTCTCC | 27342 |
| rs545856711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788573 | ATCAATTCAGTTTCT[A/G]AAAGACTTCTTAATA | 27342 |
| rs545888582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781948 | GTTAATCTGCTGTTT[A/G]TCTGTCATCCAGTGT | 27342 |
| rs545906912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738424 | CCAACCTCTTCTGCT[C/T]AGCCCATTGAACACT | 27342 |
| rs545909493 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686109 | AGACTGCGAAACCCC[A/G]TCTCTACTAAAATAC | 27342 |
| rs545931661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699647 | TGGTGAGCTGGGATC[A/G]TGCCACTGCACTCCA | 27342 |
| rs545965664 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794881 | GTGTTATAAAGCCAC[C/G]AGAAATGATTCAGTG | 27342 |
| rs545979206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787471 | GCCCCAGCCTCCCGC[A/G]TAGCTGAGATTACAG | 27342 |
| rs546015850 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699289 | TCATTCTCTGTTCCC[C/G]TAGACCGGGAGACAA | 27342 |
| rs546027209 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794258 | GTTAAAAAAATTTTT[A/T]AATTTCTTTCTTTCT | 27342 |
| rs546054445 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706167 | TCGGCCTCGCAAAGT[C/G]CTGGGATTATAGACA | 27342 |
| rs546071244 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741857 | AAAGAGTGTGTTCCG[A/G/T]CCGGGTGCGGTGGCT | 27342 |
| rs546083285 | in-del | -/AG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697002 | CAATGTGCGTGGAGC[-/AG]AGAGAGGACTGCAGA | 27342 |
| rs546100175 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | RABGEF1 | GRCh38.p7 | 7:66712187 | TTTGGGAAGCAGTGA[C/T]ATCCAACCTGTATCA | 27342 |
| rs546129043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767759 | TCATTGAACCACCAG[A/G]CACCAACATCTGTTG | 27342 |
| rs546130377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800756 | CCACCGTAGCCTTTA[C/T]GGCCTGTTGCTAATA | 27342 |
| rs546141265 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705420 | CCAGCCTGGGCAACA[C/G]AGCGAAACTCCATCT | 27342 |
| rs546158898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754718 | TTTGATTGCGCCATC[C/T]AACAAATCTGAATAA | 27342 |
| rs546167005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719152 | TGGGACAGTAGGGAA[C/T]GGCAATTAACACCAA | 27342 |
| rs546180836 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738566 | AAACCTTGTCTCTAC[-/A]AAAAAAACCCCAAAA | 27342 |
| rs546193403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807959 | CACGCCTGGCTCAGA[C/T]GTCTGTTGAATTGGG | 27342 |
| rs546219533 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760834 | GAGTCTTGCTGTGTT[G/T]CCCAGGCTGGTCTTG | 27342 |
| rs546231588 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741005 | CCGCCCTCGGCTCCC[G/T]TAATCCTCAGAGTGC | 27342 |
| rs546275035 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681524 | CCACCTCAGCCTCCC[C/T]AGTAGTTGGGACCAC | 27342 |
| rs546291307 | snp | C/G | 0.0748431 | 0.178382 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723810 | GTCTCGAACTCCTGA[C/G]CTCAGGTGATCTGCC | 27342 |
| rs546297975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707272 | ATAGTGGAGAATGTT[C/T]CATGTGTACTTCAGA | 27342 |
| rs546310813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686037 | TAATCCCAACACTTT[A/G]GGAAGCTGAGGTGGG | 27342 |
| rs546310988 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743329 | AAAAGAAAAAAATTT[A/T]AAAAAAAAAAAAAGG | 27342 |
| rs546313189 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749653 | CACTCTAGCCTGGGC[A/T]ACAAAGCAAGACTCC | 27342 |
| rs546319369 | in-del | -/TTTTG | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66738948 | AGGTACTTTGTGTTT[-/TTTTG]TTTTGTTTTGTTTTG | 27342 |
| rs546323370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748872 | CTGCACTGTTTCAGC[A/G]CCTTATTGAAACCCT | 27342 |
| rs546341371 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692910 | CTACCCCCCAGGCTT[C/G]AGGGCTGAGGCAAGG | 27342 |
| rs546344895 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755134 | CTGGTCTCTACTAAA[A/C]ATACAAAAAATTAGC | 27342 |
| rs546361210 | in-del | -/T | 0.00755907 | 0.0610114 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749363 | CTTGCCTAAATATAG[-/T]TTATGTAATGCTGTG | 27342 |
| rs546376606 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689697 | AATCCCAGCAACTCG[A/G]AGGCTGAGGCAGGAG | 27342 |
| rs546394153 | snp | G/T | 0.0501905 | 0.150254 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778281 | ATACGTAGCAGCTTG[G/T]TAGCAGACAAAATAC | 27342 |
| rs546407538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772527 | AATCTGTTGACTTGT[A/G]TACATAGTCATTGCA | 27342 |
| rs546416147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801342 | GGTAATTACCTTAGG[A/G]GAAATGGGGTCCATC | 27342 |
| rs546428541 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808506 | GGCTTGAGGCACCGG[A/G]CCCGGTCTGGAGCTG | 27342 |
| rs546452600 | in-del | -/ATAT | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688133 | ACATCAGGAGTGGCC[-/ATAT]ATATGTTAGGCAAAA | 27342 |
| rs546546052 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718964 | CATACTTCTTACGAC[G/T]GCATCTTTCTTCAGT | 27342 |
| rs546551036 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66685022 | CTCTAGCCTTGGACT[C/T]CCAAAGTGTTGGGAT | 27342 |
| rs546555866 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792471 | TATCCCCGAGTATCT[A/G]TTCCTATAGGATAAT | 27342 |
| rs546565025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66740815 | GCGGACGGACTGGGG[C/T]TGAGAGCTGCTCGGC | 27342 |
| rs546574835 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759311 | TGCATTGAGCAGATT[C/G]TACAGGACACCAGCA | 27342 |
| rs546579420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745693 | AGAATCTCTTGATCC[C/T]GGGAGGCGGAAATTG | 27342 |
| rs546615042 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737425 | CACCTGGCTATCCTA[C/T]GCAATACGAGACTGG | 27342 |
| rs546670250 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789632 | AGCTTGCAGTGAGCC[G/T]AGATCACGCCACTGC | 27342 |
| rs546678405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736926 | CATGCACAGACACCT[A/G]CGTATACAGACACAC | 27342 |
| rs546713650 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703265 | GTATGAGCCACCGTG[A/C]CTGGCCTGTATGTAA | 27342 |
| rs546724986 | in-del | -/AA/AAA | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66738731 | GTGAGACTCTAACTC[-/AA/AAA]AAAAAAAAAAAAAAA | 27342 |
| rs546725122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697946 | TGAGCCTCTTCCTTA[C/T]TGGGAAGCCCGGCCC | 27342 |
| rs546751901 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727407 | ATCCCATGGCATTGC[C/T]TTCCCTTTGAAAGTT | 27342 |
| rs546759300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699015 | CAGTCCCACATGCAG[C/T]GCTGGGACCTCTGGG | 27342 |
| rs546759827 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703528 | TGTGGACATCCAGTT[A/G]TCTCAGCACCATTTG | 27342 |
| rs546766635 | snp | C/T | 1.65737e-05 | 0.00287864 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66772007 | GCAGGGTTTCTGCTC[C/T]AAGTGCTGGAGGGAA | 27342 |
| rs546779564 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741968 | GGTGAAACCCCGTCT[C/G]TACTACAAATAAAAA | 27342 |
| rs546792718 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735597 | TGACAGGATCATTGT[C/G]GGGGGGGTTTCCCCT | 27342 |
| rs546809743 | in-del | -/GTTT | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701858 | TCTTATAAGTCTGTG[-/GTTT]GTTTATTAATTTTTT | 27342 |
| rs546849695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799583 | TGGCATTCAGAAGAG[C/T]AGGTTCTCTTTTACC | 27342 |
| rs546878483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710964 | CCTGGGCAACATAGC[A/G]AGACCCTGTCACTAC | 27342 |
| rs546911169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798886 | AGAATTGCTTGAACC[C/T]AGGATGCAGAGGCTG | 27342 |
| rs546912885 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806579 | CATGGTGGTTTAATC[C/T]GTAGTACTGAAAAAA | 27342 |
| rs546925034 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763443 | GGCTATTAGTCTCCT[C/G]CAGCTTCAAAACCAT | 27342 |
| rs546928204 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694443 | ACGGAACATAAGGTC[A/T]GGCTGGAAAGGTGGG | 27342 |
| rs546936883 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745717 | GAAATTGCAATGAGC[C/T]GAGATTGTGCCACTG | 27342 |
| rs546940424 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765854 | CTTTGTGGATTGAGA[A/G]GACAGTTTCCTGATA | 27342 |
| rs546958438 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795256 | ATTCAAACCGCCTGC[A/G]AGCCTAAATTTTTGT | 27342 |
| rs546982184 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767726 | CCCACCATGTGAGGA[C/T]ACAGGGAGAAGGTAT | 27342 |
| rs547006435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717025 | CTCAGGTGATCCGCC[C/T]GCCTCAGCCTCCCAA | 27342 |
| rs547015673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699445 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGTCGAGG | 27342 |
| rs547044089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787146 | ATCGTCCTCCCTCAG[C/T]CTCTCGAGTAGCTGG | 27342 |
| rs547045417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700325 | CTGAGCTCCTCTTTC[A/G]CCTTGAAGGGGTCCT | 27342 |
| rs547073318 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778922 | GGAGTTTGAGACCAG[C/T]CTGACCAACGTGGCA | 27342 |
| rs547127046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788115 | ACTTCCTCAAAGTAC[C/G]TACCCTTTAATTTGT | 27342 |
| rs547128568 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754802 | GTGTGTGTATGTGTG[G/T]ATCACTTTACCCAGC | 27342 |
| rs547137536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794535 | GTGAGAAACAAATAC[A/G]TATATTACACCTATA | 27342 |
| rs547156365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793538 | ATCACAAGAATGAAT[A/G]TAGTTTCTTCTAAGT | 27342 |
| rs547158329 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744380 | TCTACAAAAAAAAAA[A/T]AAAGATAGCCGGGCG | 27342 |
| rs547262190 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717655 | CCTTGACCTCCCCAG[G/T]CTCAGGAGATCTTCC | 27342 |
| rs547282055 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66682016 | CTACTCTGTGTAAGC[C/T]TTTGGATCCCGCTCG | 27342 |
| rs547286701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760289 | CTAGAGTATGTGACC[C/T]TTTAAGATGCACTTT | 27342 |
| rs547291659 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66753299 | TGCTAACTGGGGTGT[A/G]TGATTGTCCTATTTG | 27342 |
| rs547355139 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788668 | TTCATTGTTATTTTT[C/T]TAGCCAGTCCTATAA | 27342 |
| rs547356094 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752676 | GCAGTATCACCTGGA[A/G]ACTTGTTAAATTCGA | 27342 |
| rs547384018 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707447 | CCTGCAATCCCAGCA[C/G]TTTGAGAGGCCAAGG | 27342 |
| rs547416378 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682437 | CCGTTTCAGGCCGCC[C/T]TCGGTTCCCTTAATC | 27342 |
| rs547418535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795064 | GCCCACCGGGGTGGA[A/G]TTTTGGGAAGTTTGC | 27342 |
| rs547418961 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713382 | ATCGGCCCGCCTTGG[A/C]CCTCCAAAGTGCTGG | 27342 |
| rs547420113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683963 | CCACGCTGGTCTTGA[A/G]TTCCTGGACTCAAGC | 27342 |
| rs547425387 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763238 | GGTATTCTGCTGAGG[A/C]CCTCAGGAGGTCAGA | 27342 |
| rs547447266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721235 | AAAGAAAGCCATTAA[C/T]AATAGTGTTTAAAAA | 27342 |
| rs547475789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801700 | TTCATCCATGTTGTT[A/G]CAAATGACTGGATCC | 27342 |
| rs547497424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719375 | GCCCAGCTAATTTTT[A/G]TATATATTTTGTAGA | 27342 |
| rs547502779 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810501 | AGTTATCCTCCTGGT[A/G]GTTAATATGGTGTAA | 27342 |
| rs547505425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683502 | AGTTGAGGAGAAGGG[A/G]CAGTCAAGATACTTT | 27342 |
| rs547526520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760905 | AAGTGCTGGGATTGT[A/G]GGCGTGAACCATTGC | 27342 |
| rs547541395 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689540 | GGGCAAGGTGGCTCA[A/C]GCCTATAATCCCAGC | 27342 |
| rs547550890 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683866 | CCACCTCAACCTCCC[A/G]AGTAGCTGAGACTGC | 27342 |
| rs547582643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726048 | TTCAGCTCTCGGGAG[A/G]ACCTGCCAGCACAGG | 27342 |
| rs547585888 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775146 | TCTTTAGATCCTCCT[A/G]AATTAATGGAGTAAT | 27342 |
| rs547586752 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715053 | CTACTTCTTCTCCTT[C/G]TCTTTCTCTTTTTCC | 27342 |
| rs547640766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688516 | GTGTATTAGGCTGCA[A/G]AACAAGTATTAATGT | 27342 |
| rs547646300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682467 | CCTCACAGTGCGCGG[C/T]CTCTCCGTCCAACGT | 27342 |
| rs547646449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808158 | CCCACGGTCACTCAC[C/T]GTTGTTGTTAAGTGA | 27342 |
| rs547675824 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757942 | TTTGCTTGTCTGTAT[A/G]TATCAGGTTTTGTAA | 27342 |
| rs547676263 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782791 | ACTTCGTCTCAAAAA[A/G]AAAATAAAACATACT | 27342 |
| rs547701458 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739380 | GAAACTCGGGCCGGG[C/T]GCAGTAGCTCACACC | 27342 |
| rs547718016 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708370 | TTGGCTCACTGCAAC[A/C]TTCGCTTCCTGGGTT | 27342 |
| rs547729850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687958 | GGCGTGGTGGTGCAT[A/G]CCTGTAATCCCAGCT | 27342 |
| rs547741707 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774399 | TTTACAGTCTTTCTT[C/G]CTTCCCTACCACATG | 27342 |
| rs547765545 | in-del | -/TT | 0.0741063 | 0.177655 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754169 | AACACGCCTGGCTAA[-/TT]TTTTTGTATTTTTAG | 27342 |
| rs547779172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720845 | ATAAGTTAGCAGAAC[C/G]AAGTGTCAATTGAAT | 27342 |
| rs547783322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762570 | CTCTAGTCTAGGTGA[C/T]AGGGTGAGACCCTGT | 27342 |
| rs547802783 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760865 | AACGCTTGACTTTGA[A/G/T]CCATCCTCCCACCTT | 27342 |
| rs547859687 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66809885 | TTTAGACAAACTCCC[C/G]TTAAGATGTGCACTC | 27342 |
| rs547894290 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721855 | TCCTTGGTGCTTTGA[A/G]ACAGAAAGTTTTTGG | 27342 |
| rs547894758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768798 | CCACACTTTTTGTTC[C/T]CAAAGGGCTCATATT | 27342 |
| rs547900280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754104 | GCTTCCTGGGTTCAA[A/G]CGATTCTCCTGCCTC | 27342 |
| rs547911478 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727670 | CGGCCCATGCTCCCA[C/G]CCAGGCTTCTCCAGG | 27342 |
| rs547922971 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793803 | CTGACCCCAAGTGTC[A/C]TGCCATCCTTTTAGA | 27342 |
| rs547932846 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743853 | CCAGGGTGCTCTCCA[A/T]CCCCTGGCCTCAAGT | 27342 |
| rs547945777 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727118 | ATTGTATGGTGTGTG[A/T]ATTTTATTACAATAA | 27342 |
| rs547947780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733199 | CAGCCCAGGCCTGAA[C/T]AGCCTTCTCTCAAGA | 27342 |
| rs547978778 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766808 | CGGCTTACTGCAGCC[A/T]CTGCCTCCCAGGTCC | 27342 |
| rs547989323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766073 | ATTAGCTCAGACTTT[C/T]AAAATAATTTGAAAC | 27342 |
| rs548013214 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695515 | CATTCAGTGACAAGA[G/T]TTGCTGCAGCCCCTG | 27342 |
| rs548032799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732778 | CTCTCTTTCTCACTC[A/G]CTCTCTCTTGCTGTC | 27342 |
| rs548047699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701084 | GGCAGTGGGGCAGGG[A/G]TGGGGACTGTTTGTG | 27342 |
| rs548059141 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738569 | ACCTTGTCTCTACAA[A/T]AAAACCCCAAAAACT | 27342 |
| rs548068111 | snp | A/T | 0.00716266 | 0.059414 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66682047 | CACTTCCTCCCGTCA[A/T]CAGCCAAAGGCCCCG | 27342 |
| rs548070148 | in-del | -/AGAAAAAAAAGG | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743334 | AAAAAATTTAAAAAA[-/AGAAAAAAAAGG]AAAAAAAAGGCTCTC | 27342 |
| rs548071695 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743561 | GGCTGGAGTGCAGTG[G/T]CGCGATCTCGGCTCA | 27342 |
| rs548074924 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737340 | GCTCACTACATCCTT[A/C]ATCTCCTGGCTCAAG | 27342 |
| rs548107850 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697881 | AAGGTCCAGGAGTCC[A/G]AGAGCAAGTGAGGCT | 27342 |
| rs548148068 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707795 | TGAGGCTCTGTTTTT[C/T]GGTGCATATAGGCTT | 27342 |
| rs548152005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794409 | GATCCTCTAGCCTCA[A/G]CCTCCCAGAGCACTG | 27342 |
| rs548191112 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706327 | TTCATTTCTCTTATG[C/T]GATACCTAGGAATGA | 27342 |
| rs548215057 | snp | A/G | 0.000181391 | 0.00952169 | missense | RABGEF1 | GRCh38.p7 | 7:66809165 | GAAGTTCAAGACATC[A/G]TTGAGAAATACCCAC | 27342 |
| rs548224627 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720307 | GGCTCAAGAAATTCT[C/T]GTGCCTCAGCCACCC | 27342 |
| rs548266100 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808103 | GTGGTATTTCCCCCC[A/G]TTTACAGGTACAGAA | 27342 |
| rs548269073 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682352 | GACGTCCGCGCGGCC[C/G]GGACAGTTGCGCGTC | 27342 |
| rs548277919 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689725 | GAGAATCACTTGAAC[C/T]CGGGAGGCGGAGGTT | 27342 |
| rs548286991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768709 | TTTGGTACGGAATAG[C/T]GTCAGATCCATGCAT | 27342 |
| rs548294255 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725189 | GTACATCCTTTTACA[G/T]CTTTATCAAGATACA | 27342 |
| rs548308755 | in-del | -/A | 0.362732 | 0.22314 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804739 | GTGAAACTCAGTCTG[-/A]AAAAAAAAAAAAAAA | 27342 |
| rs548325745 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807171 | ACTTAGCAGCTTCTA[G/T]TGCCCTTGGCCTGCA | 27342 |
| rs548364367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687875 | CAGATCCCTTGAGGT[C/T]GGGAGTTCAAGACCA | 27342 |
| rs548371498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773730 | GAGTGCAATGGTGCA[A/G]TTTCAACTTACTGCA | 27342 |
| rs548380730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788623 | CTTTCTAAGGAAGCA[A/G]TTAAGCACAACATAA | 27342 |
| rs548397348 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778241 | ACTTGCTTCTGTTAG[G/T]AGCATAAAGGAAAGT | 27342 |
| rs548434730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780235 | ACTGAGGTAGTTGTA[C/T]TACCTCATAGTCAGT | 27342 |
| rs548443482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787917 | TATTTATATGAAAAC[A/G]CTCACTGTAAGACAC | 27342 |
| rs548445990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700979 | CAGTGTGGTGGGCAG[C/T]GCTGTCTTGCAGCCC | 27342 |
| rs548458722 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741670 | GGAGAGCTGCTTTCC[C/T]CCCTCTAAACCTAGA | 27342 |
| rs548544190 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740066 | CAACTTCCTGGGCTA[A/T]CAAGCGATCCTCCCA | 27342 |
| rs548563380 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683455 | TTAATGACCTTTCCA[A/G]TCAGTCAGTTTCTGC | 27342 |
| rs548654907 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739518 | AAAAAAAATATGAGC[A/T]GGGCGTGGTGGCGGG | 27342 |
| rs548694145 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775082 | CGTCCATCCTGTAGC[A/T]ATGTGAGACCTCAGA | 27342 |
| rs548711152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738457 | TTCTGGGCCCAGGGG[C/T]CTAGGCTCATGCCTG | 27342 |
| rs548741073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702451 | TGTGAACCTTCATCT[A/G]CAAGTTTTTGTGTGA | 27342 |
| rs548772494 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714366 | GACTTGTTCATAATA[A/T]CCCCTTATTATCCTT | 27342 |
| rs548773870 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743439 | AAGCTATCCTCTTGT[C/G]TCAGCCTCCCAAGTA | 27342 |
| rs548775548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789896 | CTCAGTTCTGCACAC[A/G]GCTACAAAACAAAAG | 27342 |
| rs548791938 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744368 | CAAGACTGCATCTCT[A/C]CAAAAAAAAAAAAAA | 27342 |
| rs548803858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700235 | GCCAAGCCCCACTGC[A/G]ATGGGGCCAGATCCA | 27342 |
| rs548823099 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802454 | GCTCTGTGTTTCCTA[A/T]TCATGTGAAGGCAGA | 27342 |
| rs548840594 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706883 | GCCTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC | 27342 |
| rs548858066 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720617 | GATAAAGTATGAATT[G/T]TTTCTCCCTAAGATT | 27342 |
| rs548891367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720258 | GTTGGAGTGCAGTGG[C/T]GCGATCTCGGCTCAC | 27342 |
| rs548914089 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748391 | GGATCTTTTGTAATG[A/T]ATTTATCAGCAGTGG | 27342 |
| rs548931803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752071 | AACTAGCCAGGTGTT[A/G]TGGCTTGAACTCAGC | 27342 |
| rs548952044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696579 | CCTGAATTCCCAGCT[A/G]TTTGGGAGGCTGAGG | 27342 |
| rs548990835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776405 | CTCTTTAAGACATGG[A/G]TACCAGACCTGGTGC | 27342 |
| rs549007188 | snp | C/G | 1.80029e-05 | 0.00300019 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783630 | GTAATTCCATGCATG[C/G]ATCTTTTATGTCATG | 27342 |
| rs549037284 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727615 | AAATTGAGTCTGACA[A/C]CTGGCAAGGCCCACA | 27342 |
| rs549039733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696041 | TGGGTGGGGCTGGAC[A/G]TGGGCCTTACAAGGG | 27342 |
| rs549044344 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751613 | AGGTTGGATAAGGCC[C/G]CATTTTGCTCTGATT | 27342 |
| rs549090984 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66685197 | GTCTTGCTCTGTCGC[C/T]GGGCTAGAGTGCAGT | 27342 |
| rs549092582 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706355 | TGAAGTGACTAGGTC[A/G]TACGATAGGTATGTA | 27342 |
| rs549107710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757889 | GTGCTGGGATTACAG[C/G]CGTGAGCCACTGCGC | 27342 |
| rs549111821 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792618 | CACTATCTCTGTCTC[C/T]TAAAGCTGTTTTCTA | 27342 |
| rs549157427 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798127 | TTCTCAAAAAAATAA[C/G]AAGTCAGTAGATGTC | 27342 |
| rs549181575 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763315 | AGTCTCCTTCCAGAT[A/G]CACTCGTGTTGGCAG | 27342 |
| rs549206762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795788 | CTTTCCAGGAGCAAT[C/T]GGATAATTTATTGAG | 27342 |
| rs549221760 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756194 | AGTGCTAATAAATAT[C/G]TCTAAAGATGGCTAA | 27342 |
| rs549263752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763897 | AGTTGATGTACATTT[A/G]GGTTGTTTCTGCTCT | 27342 |
| rs549308933 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801137 | CCACCCCAGGAAGGG[A/G]ATCAGAGAGTCCATC | 27342 |
| rs549323538 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745171 | CACTCCAGCCTGAGC[C/G]ACAGAGCGAGACTCC | 27342 |
| rs549325673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703411 | TTCTTCTAAGAATTC[C/T]ACAATTTTAGCTCTC | 27342 |
| rs549326962 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728457 | GGAAGTTGCCTCTGC[A/T]TGTTCCTGTTCCCAC | 27342 |
| rs549329147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771127 | TGTGTTTTGCAGATA[C/T]TTAATTTTTAAAAAT | 27342 |
| rs549337672 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745981 | AAGAAGTTTCATAGT[A/C]CAGGCCAAACATCTT | 27342 |
| rs549365680 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727675 | CATGCTCCCAGCCAG[C/G]CTTCTCCAGGCCAGC | 27342 |
| rs549407008 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790866 | CTACAGGTCTTCTAG[A/C]GTTCATGAATCACGC | 27342 |
| rs549427421 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797980 | AAATTAGCCAGGCAT[A/G]GTGGCGCACGCCTGT | 27342 |
| rs549440092 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794938 | AATATGTAAATTATC[A/G]AAACATGCATTAAAT | 27342 |
| rs549460064 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804693 | TGAGCAGAGATCACA[C/G]CACTGCACTCTCCAG | 27342 |
| rs549481753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66738768 | ACACTCATTCTGTTT[C/T]ACAGAATGGTTTATA | 27342 |
| rs549512009 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749262 | ATAGTTCAAATTTAT[C/T]AAATGCTAGCAGGAG | 27342 |
| rs549557490 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782362 | CTTTTGTTACTAGTT[A/T]CTTGTGTATCCTTTT | 27342 |
| rs549566682 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721412 | AAGATGTCACAGATT[C/G]GCCTTCTGGAGGCTC | 27342 |
| rs549571386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719923 | TGGTCCCTGATGTGG[A/G]CCAGCAGTCTTCATG | 27342 |
| rs549572564 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729689 | CCATCACCCATCCAG[G/T]CTCCAGGTGGGTCTC | 27342 |
| rs549594225 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749775 | AGGAGATAGAGACCA[G/T]CCTGGCTAACACAGT | 27342 |
| rs549605588 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728013 | GGCCAAACCACTAGA[C/T]CCAATGTCCCCCTTC | 27342 |
| rs549661130 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719451 | CTCAAGCACCTCGGC[A/C]CCCCGCAGTGTGCTG | 27342 |
| rs549661141 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726899 | GTCCCAGCTACTTGG[A/G]AGACTGAGGCAGGAG | 27342 |
| rs549679048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770348 | TGGAGAAGAATGAAG[A/G]CCATGTGGTTTCAGT | 27342 |
| rs549686402 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752825 | CTTGTCAGGTTAGTT[G/T]TTTGCTGTTTAATTT | 27342 |
| rs549691113 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699975 | ATGTGGGCACAGTTA[C/T]CTTCATCCTCTCCGG | 27342 |
| rs549694693 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810693 | TCCACAGATTATGCA[C/G]CTATACTTGTGAAAT | 27342 |
| rs549695889 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726236 | GCTTATTCATATCTG[C/T]TGGGTGGTAGTGCCT | 27342 |
| rs549713293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691514 | GACCCAAAAAACATA[C/T]ACACATGGTCTGTGA | 27342 |
| rs549729748 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754972 | TTGAGGCCAGGAGTT[C/G/T]GAGACCAGCCTGGGA | 27342 |
| rs549734351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782859 | GATATGGGGAACTTA[A/G]TTTCCTTATAAACAT | 27342 |
| rs549757989 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701690 | ATTTTTGTATTTTTA[A/G]TAAATACAAGGTTTC | 27342 |
| rs549798976 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801063 | TAAAATTTTGAAAGT[C/T]ATCAAGTCCTCTGCC | 27342 |
| rs549802444 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683297 | GCTGTTAGTCTGTTC[C/T]TTAAAATTGTTGTAC | 27342 |
| rs549815319 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689146 | AAATCAGTCACCTAA[C/G]TATACACTTTAAAGG | 27342 |
| rs549834439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707484 | GATCACCTCAGGAGT[C/T]CGAGACCAGCCTGGC | 27342 |
| rs549840079 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732710 | TGCTCTCTCTCTCTC[A/G]CTCACTCTCTCTCGC | 27342 |
| rs549846030 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714447 | GATAATTTATGTCTC[A/G]TTTCCTTTCTTTTCT | 27342 |
| rs549857201 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788717 | GGCACAGTGGCTCAC[A/G]CTTGTAATCCTAGCA | 27342 |
| rs549899015 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763264 | TCAGAATTAAGCATC[A/G]GCCAGCCTGGGTTTT | 27342 |
| rs549906025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755481 | ATCCTATGTCAAGAA[A/G]AGAAAAGAAAAAAAA | 27342 |
| rs549936314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803844 | CAGTGAGCCGAGATC[A/G]TGCCACTGTACTCTA | 27342 |
| rs549957834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762706 | AAGAACACGCCTCTA[C/T]CCTCTCCTGCCACCC | 27342 |
| rs549958711 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708838 | TACAACAACAGAAAA[A/G]TAGGTTTTGTTTTGT | 27342 |
| rs549961055 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693911 | CTCTGGGGCTCAAGC[A/G]ATTCTCCTGCCTCAT | 27342 |
| rs549961957 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770025 | GTCTCTCTATACTCC[A/G]TAAGTGAGAATTCCT | 27342 |
| rs549971259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761677 | AAGACCAATCCAGAA[C/T]AGAGTCCTGCCTTGG | 27342 |
| rs550011498 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684718 | TGGCTCACTGCAAGC[C/T]CCGCCTCCAGGGTTC | 27342 |
| rs550035212 | in-del | -/AAAG | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803901 | CTCAAAAAAAAAAAA[-/AAAG]AAAGAAAGAAATTTT | 27342 |
| rs550041866 | snp | C/G | 8.2426e-05 | 0.0064192 | missense | RABGEF1 | GRCh38.p7 | 7:66809016 | GTTGGTCTCCTGATG[C/G]TTGCTTAGGCGTCAA | 27342 |
| rs550103593 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724082 | TTGTTTCTTAAGAAA[-/T]TTTTTTTTTGTCTTC | 27342 |
| rs550104089 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691297 | AGAGAAATTAAAAAT[A/C/T]TACATCTACACAAAG | 27342 |
| rs550107143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750921 | TGCTGTTAAATACAC[A/G]GTTTGAATTCTTAAT | 27342 |
| rs550141265 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810014 | GCTGTTTAATGTAGT[C/T]GATGGAAGACTTTAA | 27342 |
| rs550166339 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710302 | GATGGACATTTAGGT[G/T]GTTTTTTAGCGTTTA | 27342 |
| rs550168506 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757111 | TTTGTAGTAAACTTA[C/G]ACATTTTGGAATGTT | 27342 |
| rs550179747 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783486 | TTTGTCTACTCATAC[A/T]TCCTACTTGTAAAAC | 27342 |
| rs550207958 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722068 | CCAGCTAGGCAGGAA[G/T]ATCACTTGAGCCCAG | 27342 |
| rs550287276 | snp | A/G/T | 0.00636936 | 0.0560724 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811077 | TTGGTTTAATTTTCT[A/G/T]TGTGCTTTTAGGTGT | 27342 |
| rs550290267 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726706 | GGATAATGAAATGGT[C/G]TAAAATGGACTGCGA | 27342 |
| rs550295932 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686017 | GGTGCGGTGGCTCAC[A/G]CCTGTAATCCCAACA | 27342 |
| rs550314383 | snp | C/T | 0.00033961 | 0.0130265 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66771920 | CCTTAAGTCTGAACG[C/T]CGAGGAATTCATGTG | 27342 |
| rs550322571 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729495 | CTCCATCCTCACCTC[C/T]ATCCTCACCTTCAAC | 27342 |
| rs550323396 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697139 | GGGGTGCAGAGCAGG[A/C]GTGAGAGGGGCTGGG | 27342 |
| rs550339466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684122 | ACAGAACCAGGGAAG[A/G]GTTTTTAGCTGGGTC | 27342 |
| rs550355126 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725165 | ATTTTCCCACTTCCT[C/T]ACATGTCTGTACATC | 27342 |
| rs550375450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778131 | ATTAGCCTAAGTGCC[A/G]TTTTAATGTATTAGG | 27342 |
| rs550398240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735514 | TGAAATGGTTTGGTT[C/T]TGTGCCCCTGCCCAA | 27342 |
| rs550403262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784472 | CAGTGGCAATAATTA[A/G]TAAGACTGCCTGTAA | 27342 |
| rs550415777 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727697 | CAGGCCAGCCCCTCG[C/G]AGGGGTCCTGGCGGT | 27342 |
| rs550420894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775849 | TTGTGTCTTGAGGAA[A/G]TGTATTGAGAACATA | 27342 |
| rs550430148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696441 | ACGCCTGTAATCCTA[A/G]CACTTTGAGAGGCCA | 27342 |
| rs550479156 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790213 | AAAGACAATAACCCT[C/T]ACCTGAAGAACCTCT | 27342 |
| rs550489301 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680857 | AAGGCCAAGGCGGGC[G/T]GATCACTTGAGGTCA | 27342 |
| rs550519016 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695980 | AAAAAAAAAAAATAA[A/G]GTGTAGATGACTCTT | 27342 |
| rs550532235 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741898 | ATCCCAGCATTTGGA[A/T]GGCCAAGGCAGGCGG | 27342 |
| rs550536707 | in-del | -/TCTC | 0.00159744 | 0.0282165 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732762 | CTCGCTCTCTTGCTG[-/TCTC]TCTTTCTCACTCGCT | 27342 |
| rs550546332 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772422 | CCCACTGCAGGGCTT[A/G]GAAATGGCACTCATC | 27342 |
| rs550549314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703308 | GATGAAGTTCAACCT[A/G]TCTATTTTTTCTTTT | 27342 |
| rs550565011 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745990 | CATAGTACAGGCCAA[A/T]CATCTTGAAAATCTT | 27342 |
| rs550588886 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764795 | GGTTTATTTCTGGAA[C/T]CTCAATTCTATTCCG | 27342 |
| rs550645553 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751428 | GTTTCTATTATCTGC[A/G]TTTCCTGTTGGTTTT | 27342 |
| rs550646703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741494 | CTGCCGCTTTGGAGG[C/T]TAGGTCATAGGCAGC | 27342 |
| rs550690245 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722169 | CTCAGGGGCTGGGTA[C/T]GGTGGCTCACGCCTG | 27342 |
| rs550692520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734841 | CTTCCTCCTGCTCGG[C/T]TGGTCACTCCTGCAC | 27342 |
| rs550701775 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime | RABGEF1 | GRCh38.p7 | 7:66740730 | GAGCTGGCCGCGGAG[C/T]CCAGACCTACCCGGG | 27342 |
| rs550733339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777626 | GAGTCTGTACTTTAA[A/G]AAGAAACATTTCTGG | 27342 |
| rs550766453 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740573 | CAGGGCGGTACCCCA[C/T]TCCGCTCGACCCTTT | 27342 |
| rs550775058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704952 | ACTGTCTTCCAAAAT[A/G]GCTATACCAATTTGC | 27342 |
| rs550822088 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695898 | TTACATCTGGGAGTC[A/G]GAGGTTGCAGTGAGC | 27342 |
| rs550834729 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767059 | CCAGGCTGGAGTGCA[A/G]TGGCATGATCTTGGC | 27342 |
| rs550844496 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746428 | CTGCCTCAGCCTCCC[A/G]AGTAGTTAACCACCA | 27342 |
| rs550857062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752575 | AAAAGGGAGTCTCCC[A/G]TTGGGAATGAAGTCC | 27342 |
| rs550861094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710877 | AGGCCAAGACAGGAG[A/G]ATCACCTGTAATCCC | 27342 |
| rs550927387 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734597 | ACCATGCCTGGCTAA[-/T]TTTTTTTTTTTTTTT | 27342 |
| rs550938727 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798822 | CAGAAATTAGCTGGG[A/C]ATGGAGGTGGGCGCC | 27342 |
| rs550994093 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680968 | GGCGCCTATAATTCC[A/G]GCTACTCGAGAGGCT | 27342 |
| rs551036191 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747090 | TGAGCTACCGTGCCC[A/G]GCCCTAGTGGAACAT | 27342 |
| rs551037515 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801780 | ATTCATCTGTTGACA[A/G]ACACCCTTTCCCATT | 27342 |
| rs551038221 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711656 | CAGTGGCACAATCTC[G/T]GCTCGCTGCAAGCTC | 27342 |
| rs551038866 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789017 | GGACTTAAAGCTTTG[C/T]ACCTGAATGAGGACA | 27342 |
| rs551045187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692134 | TCTGCAGTTGCACTA[A/G]TTACATTTCTAGCAC | 27342 |
| rs551049954 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793045 | TGTATTGTAAAATTA[C/T]AGGGGTTGTGCTGGG | 27342 |
| rs551054971 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776578 | TGTGCCTGTAGTTCC[A/G]GCTGAGGCCAGAAGG | 27342 |
| rs551132752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697101 | GTCAACCAGGAAGCA[C/T]AGTCATGGTGGTGAG | 27342 |
| rs551165406 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784406 | AGCTAGATTTTGCCA[A/G]TGTCAACCAGAACTT | 27342 |
| rs551170372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688213 | ATGAAAAGTTTAATC[C/T]AACAAGAAGATATAA | 27342 |
| rs551178424 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740562 | CTCTTGGGCGTCAGG[C/G]CGGTACCCCACTCCG | 27342 |
| rs551209277 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708613 | GTTTGAGACCAGCTT[A/G]GGCAACATAGGGAGA | 27342 |
| rs551215944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759213 | TTTCGTAATTCGTTC[A/G]AGGCTCTCACAGGAC | 27342 |
| rs551273841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790637 | CTTTAAATCACTTGC[C/T]GTAGTTCATGAAAAG | 27342 |
| rs551278779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803173 | ATGTAATTCACACAG[C/T]AGCCTCATAAGTAAG | 27342 |
| rs551288524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729950 | CAGGGCCACCTGGCT[C/T]ATGGAGGCCCAGGAG | 27342 |
| rs551295256 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768376 | TTTTTGCTCATTTTT[-/A]AATTGGGTGGTTTGT | 27342 |
| rs551328540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765345 | ATTGTTATTGTTTCT[A/G]TCTAATACATAGTGA | 27342 |
| rs551330301 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746343 | GAGTCTTGCTCTGTT[G/T]CCCAGGCTGGAGTGC | 27342 |
| rs551371770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715005 | CGTCGTCCTCCTCCT[C/T]CTCCTCTTCTTCTTC | 27342 |
| rs551397866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777568 | CAAAAGCCTCTGTAC[A/G]GTGTGCATTATACTA | 27342 |
| rs551440408 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745815 | AACCAAGAGTTTCAG[G/T]CTGGTGCAGTGGCTC | 27342 |
| rs551460242 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740177 | GTGACCTTGCTCTGT[G/T]GCCCAGGCTGGTCTC | 27342 |
| rs551463239 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785806 | GTGAACCTGGGAGGC[A/G]GAGCTTGCAGTGAGC | 27342 |
| rs551472934 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696630 | AGGAGGTGGAGGTTG[C/T]GGTGAGTCCAGGTCA | 27342 |
| rs551475470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776469 | AGGCCAAGACAGATG[A/G]ATTACCTGAGCTCAG | 27342 |
| rs551486345 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794841 | GTGGTAGAGGAGAGT[C/T]GAAGAAGTCAGTTAA | 27342 |
| rs551519884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744394 | AAAAAGATAGCCGGG[C/T]GCAGTGGCTCACGCC | 27342 |
| rs551567077 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709796 | AAAGAAAAAAGAAAG[A/C]AAGCAAATATTCCAG | 27342 |
| rs551569569 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722969 | ATTACTGTTTCTTTT[A/C]TTTTTTTCTTTTTTT | 27342 |
| rs551642359 | snp | A/G | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755807 | AGAACTCATTCCTTG[A/G]GAATGCTCCCCTGCT | 27342 |
| rs551655847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729334 | TCATCTCCATCCTCC[C/T]CTCTGTTCTCCCTTC | 27342 |
| rs551693702 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728514 | CCCACAATGGCATTC[A/C]CATTTCACCATTGCC | 27342 |
| rs551698890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764667 | ACATCTAACATCGTT[C/T]TTTTGCATGTGGCTA | 27342 |
| rs551711322 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697717 | GTTCTCCGGCCTCAG[C/T]GAGGTGGGGGGTGTT | 27342 |
| rs551713933 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804782 | TACAGTCAGGTAGAC[A/T]TGGTTTCAAATTCCC | 27342 |
| rs551721301 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66740872 | GGCGTCTCGGGCTGG[C/G]GGTGGCAGGGCGGTC | 27342 |
| rs551741957 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777845 | TTTTGTTTTAAAAAT[A/G]TGTATGCAGAATGAT | 27342 |
| rs551743050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749952 | GCACTCCAGCGTGGG[C/T]GACAGAGCGAGACTC | 27342 |
| rs551759108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704910 | CCTTGCAGCTGGCCT[A/G]TATTTAGTTTTTTAA | 27342 |
| rs551778214 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742099 | GAGGTTGCAGTGAGC[C/T]GAAATCGTGCCACTG | 27342 |
| rs551785478 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706571 | TGTGCCACCACGCCC[A/G]GCTAATTTTTTGTAT | 27342 |
| rs551786345 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799641 | TTTCTTGGGCATTAA[A/T]CTAAACTAAGGTCAA | 27342 |
| rs551791236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785380 | AGTGTGAAGTCTGCA[C/T]ATACCATATATGAAA | 27342 |
| rs551823458 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66682031 | CTTTGGATCCCGCTC[C/G]CACTTCCTCCCGTCA | 27342 |
| rs551843321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704139 | TTATCCCCATCTGGC[A/G]CTAGCAAGCCACACT | 27342 |
| rs551846668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66753350 | GAACCCAGAGTTCGA[C/T]GTAAATTTGTGGAAA | 27342 |
| rs551851588 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791504 | CAAAAAAATATGGAC[A/C/G]TGAAAGCTAATACCT | 27342 |
| rs551856460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711832 | ACCTCATGATCTGCC[C/T]GCCTCGGCCTCCCAG | 27342 |
| rs551861985 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681576 | GCTGATTTGTAAAAT[C/T]TCTTTTGTAGAGATG | 27342 |
| rs551888314 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765996 | ACTTAAAAATAGGTA[G/T]CTTCCTTTTGCCCAT | 27342 |
| rs551893299 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717821 | CGCCTTGGCCTCCCA[A/C]AGTGCTGGGATTACA | 27342 |
| rs551907804 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759733 | AACCAGATCTCACAA[G/T]CACAGAACCACAGGG | 27342 |
| rs551917487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798188 | TTTTTCAGCATTCCC[C/T]AGTCACATCTTTCAC | 27342 |
| rs551949696 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765601 | CAGGACGTACAGGAC[C/T]TTCTACTTTTCTCTG | 27342 |
| rs551951734 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773087 | GCTAGTTGTTTGTTT[G/T]TTTTTTTTCATCCAG | 27342 |
| rs551965258 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708128 | TATTCCTTGGTTCTT[C/T]CATTATAGCCCTCCT | 27342 |
| rs551967130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757991 | TTTTCTAACTGGAAA[A/G]AAAATTTAAGGGAAA | 27342 |
| rs551976961 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762055 | CGAGACCCTGTCTCA[A/G]AAAAAAACAAAAAAA | 27342 |
| rs551979124 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806709 | AATGCAGTGGTGTGA[G/T]CTCAGCTCACTGCAA | 27342 |
| rs551998768 | snp | C/G | 0.00517822 | 0.0506191 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680899 | CAGCCTGGCCAACAT[C/G]GTGAAACCCCGTCTC | 27342 |
| rs552019910 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683012 | AAATGTGTCGTGGGC[A/G]TCCGTGGGCTCGTTT | 27342 |
| rs552035780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66685881 | GCAAACATCTCTAGC[A/G]GAGATGACCTATCCC | 27342 |
| rs552035838 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680287 | GTTTCGCTCTTGTTG[C/T]CCAAGCTGGAGTGCA | 27342 |
| rs552049298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722259 | AGCCTGGCCAACATG[A/G]TGAAACCCCACCTTT | 27342 |
| rs552081364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686587 | GGCTGAAGTGAGTTT[A/G]AATAATCTAGACTGT | 27342 |
| rs552088165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719902 | ACTTTACAGAACAAG[A/G]TTTGCTGGTCCCTGA | 27342 |
| rs552099612 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697734 | AGGTGGGGGGTGTTC[A/C]TGTTTGAAGTGGCCG | 27342 |
| rs552104717 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760198 | TCTTCCTTGCCTTCG[A/C]CACTCTTAACCTGGA | 27342 |
| rs552121762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66685392 | AGGCATGTTGGCTCA[C/T]GCCTGTAATCCCAGC | 27342 |
| rs552161187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779241 | TGGCACAGGGGCTCA[C/T]GCTTATGATCCCAGC | 27342 |
| rs552176177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807046 | AACCTGGAAGTCCCT[A/G]AGAAGTGTGAAGGTG | 27342 |
| rs552191671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741345 | TTGAAGCCTGTGGTC[C/T]TGACTTCCACCCCGT | 27342 |
| rs552209755 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710867 | CCATTTTGGGAGGCC[A/C]AGACAGGAGGATCAC | 27342 |
| rs552233250 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752039 | CTATATAAACAAACC[-/A]AAAAAAACCCGCAAA | 27342 |
| rs552253775 | snp | C/T | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759797 | ATGATCAGATCACCT[C/T]TCACAGGCCCCACTT | 27342 |
| rs552261325 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693586 | CCACCCTGCCCTCTC[C/T]CATGGAGTTAAGAAT | 27342 |
| rs552270694 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739015 | GAGTGCAATGGCGCA[A/G]TCTCAGCTCACTGCA | 27342 |
| rs552272145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700130 | AGGCTTGGGTGAAGG[A/G]AGGGACGGAGGCCCA | 27342 |
| rs552297026 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724428 | GCAGTGGCGCGATCT[C/T]GGCTCACTGCACCCA | 27342 |
| rs552335582 | snp | C/T | 0.0876345 | 0.190099 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723826 | CTCAGGTGATCTGCC[C/T]ACCTTAGCCTCCCAA | 27342 |
| rs552335698 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730690 | AGCCTCCCAAGTAAC[A/T]GGGATTACAGGCATC | 27342 |
| rs552344399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693868 | GCTGGAGTGCAGTGG[C/T]GAGATCTCGGCTCAC | 27342 |
| rs552345169 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731756 | GTCTGCCAGGAGAGC[C/T]ACCCTCCTGTGCCAC | 27342 |
| rs552377210 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736764 | TACTCAGGAAGCTGA[C/G]GTAGGAGAATAGCTT | 27342 |
| rs552389920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691103 | CTCAAAAAAACAAAA[A/G]GAAAATGACAACACC | 27342 |
| rs552396089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737446 | ACGAGACTGGGTAGG[A/G]GGGGGCAGTCTAAAA | 27342 |
| rs552398541 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706416 | TTCCAAAGTGGCTGT[A/C]CTATTTTGTTTTTAG | 27342 |
| rs552422093 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730145 | GCAGCACTTCCTCAC[A/G]TCCACGGAGAGTGCA | 27342 |
| rs552439723 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705988 | GCTCACTGCAAGCTC[C/T]GCTTCCCGGGTTCAC | 27342 |
| rs552480500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780424 | AGACTTGTGAGGATT[A/G]TACAAAATAACATTG | 27342 |
| rs552520954 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697958 | TTATTGGGAAGCCCG[A/G]CCCTCTCCATCCCCA | 27342 |
| rs552538318 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688615 | GTAACCAGCAAAACT[C/T]GAAAACTCACAAATA | 27342 |
| rs552575801 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694746 | CCAATGGGACAGAGG[G/T]TGGAGGGGAGGGGGA | 27342 |
| rs552585253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798373 | GGGGAGAAGGGACTC[A/G]GAGTCCCAGGTTCCA | 27342 |
| rs552613365 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774448 | GGCTCAGCAATCAAG[A/C]TTCCCTACCCTCTGG | 27342 |
| rs552632358 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737935 | GCAGCACAGCTGGCT[C/G]CCTCATCTTTTATTC | 27342 |
| rs552648785 | snp | A/C | 1.64749e-05 | 0.00287005 | missense | RABGEF1 | GRCh38.p7 | 7:66805193 | AAGCTGGCCTGCATC[A/C]CCAAGTGCAGCAAGC | 27342 |
| rs552653096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804293 | GATGCTTTGTGTAGT[A/G]GCCACATTTCTAAAA | 27342 |
| rs552676771 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773872 | GGTTTCACCATGTTG[A/C]CCAGGCTGGTCTCAA | 27342 |
| rs552705674 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784527 | TTAATTCTGTTGTAA[C/T]ATTCTATAACCATTA | 27342 |
| rs552708421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66685513 | AAAGAAAAGATTCTT[A/G]AAGTGAATGTATACT | 27342 |
| rs552709492 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742986 | ACAGAACCAGGGGAA[G/T]TTTTTTAGCTGGGTC | 27342 |
| rs552714138 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787830 | GTGTTAACCTTTCCC[A/G]TAATAACTAGAAAAC | 27342 |
| rs552716267 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811342 | ATCAATACAACGGCC[A/G]GAGTTTCTGTTTTTG | 27342 |
| rs552770864 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742598 | GGCCAGTAACTACAA[G/T]GAGGTGCCTATTAAT | 27342 |
| rs552795467 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66685093 | TTATGTAGCTCTTAC[A/G]TACAGGCTGCTATAT | 27342 |
| rs552803587 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708508 | GGGTCAGGCTGGCTT[C/T]GAACTCCTGACCTCA | 27342 |
| rs552813235 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680540 | TGAGCCACCGCACCC[A/G]GCCATACTTTTGTTT | 27342 |
| rs552822755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712396 | TCTTTTGTTGCTAGC[A/G]CATAAATACACAATT | 27342 |
| rs552827559 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722625 | TTATGCTTACCTTTT[A/C]TTCTAAGAGTTTTGT | 27342 |
| rs552828288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691825 | TTGGGAGACTGAGGC[A/G]GGAGGATCACTTGAG | 27342 |
| rs552875237 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754003 | AGCCAACGTACTAGG[C/T]CATTTTTTTTTTTTT | 27342 |
| rs552880514 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764252 | CTTTTCATATACTCA[C/G]GACTGTTTGCATATC | 27342 |
| rs552883250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747726 | GGTACTTTGGAGCAC[A/G]TAAAAGAAAATGCCA | 27342 |
| rs552894615 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771405 | CAGCCTCCCAAAGGG[C/T]TGGGATTACAGGTGT | 27342 |
| rs552898720 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781335 | TAAAATAATCTTAGA[C/T]GGGAATTTTTAAATG | 27342 |
| rs552915381 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728722 | TTCAGCTCTGTCCTC[A/G]CCTCCACCTTCACCT | 27342 |
| rs552948284 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808666 | GCACCTGGGGAGGCT[A/G]CACCCAGACATCGGC | 27342 |
| rs552969173 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680978 | ATTCCGGCTACTCGA[A/G]AGGCTGAGGTGGGAG | 27342 |
| rs552983861 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723244 | AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACCA | 27342 |
| rs553022494 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797827 | GAAGCTGTGAATATC[A/C/G]GTATCAAGGCAGGGG | 27342 |
| rs553051816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736382 | TAGTCTCAGTGCAGT[A/G]AACAACCTATACCAC | 27342 |
| rs553094536 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786890 | TGTCATTAACACAAA[A/T]TCCTTTTATGTTGAA | 27342 |
| rs553095085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765719 | TCAAGAGAACAGCCC[C/T]GACTTAGTCCCATTT | 27342 |
| rs553113763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724116 | TGAGAGAGGCTATTT[C/T]AATTGAATAAAGAAT | 27342 |
| rs553114403 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749738 | GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC | 27342 |
| rs553115256 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735882 | CAGTGCAAGAACAAA[C/T]GAATACAGAGGCCTG | 27342 |
| rs553126879 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750843 | TCATTCTTCAGCAGA[C/T]GCTTTATGTGTATTT | 27342 |
| rs553128571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758131 | GGAATGACCTCTGAG[A/G]GCATGACATTGAACC | 27342 |
| rs553132756 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810052 | TTCTAGCTTATTTTT[C/T]CCTCATTCATTCAGC | 27342 |
| rs553155804 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705079 | ATTTTTCACTTCAAA[G/T]TCTATTTGTTCCTTG | 27342 |
| rs553198175 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770816 | ACAGTAGCCATCCTA[A/G]TGGGTGTAAAGTGAT | 27342 |
| rs553212720 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771584 | CTAGGAGTTTTCTAG[C/T]TTGCAGCCTTTACAT | 27342 |
| rs553287218 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727313 | GGGACAGGGTGAGTC[-/AG]GGGATTGAATTGGGG | 27342 |
| rs553319123 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766138 | AGCTCAGGAGTTCAA[C/G]ACCACCTGGGTAACG | 27342 |
| rs553331213 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776204 | CTGTTCTCTGGGAGC[C/T]CCCTCACTTGCTCCC | 27342 |
| rs553338011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774016 | GCTAATCCAAAGCCA[A/G]ATTTATTGCTTTTAT | 27342 |
| rs553345267 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693990 | TTTTTTGTATTTTTA[A/G]TAGAGACGGGGTTTC | 27342 |
| rs553353052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734525 | GGTCTTGAATGCCTG[A/G]CCTCAAGTGATCCGC | 27342 |
| rs553358545 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687349 | CAGGTCAGTCTCAAA[C/T]TCCTGAACTGAGGTG | 27342 |
| rs553365460 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime | RABGEF1 | GRCh38.p7 | 7:66712221 | CTTCTAATCTGTGAA[C/T]ATGGTATGCCTCTTC | 27342 |
| rs553366950 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806137 | GAGACTTGGGGCAGC[A/G]TATGGACTTGGTTTT | 27342 |
| rs553367549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66740964 | CCACATTCCGTCTCC[G/T]TCAGCGCCGCCTTCC | 27342 |
| rs553381956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704576 | AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 27342 |
| rs553401235 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780738 | TTAGTATATATATAT[G/T]TAGGGTTGCTGTGAC | 27342 |
| rs553405943 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773430 | AGACTTAGCACCTCC[A/C]CCTGTGATTTTTGTT | 27342 |
| rs553410758 | in-del | -/CA | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770184 | TAGCTCAATTCTCTG[-/CA]CACACAGTTGGCACT | 27342 |
| rs553428700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745909 | AGGCTGCAGTGAGCT[A/G]TGATCAAGCCACTGC | 27342 |
| rs553443829 | in-del | -/A | 0.00119737 | 0.0244387 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66682052 | CTCCCGTCATCAGCC[-/A]AAAGGCCCCGGAAGT | 27342 |
| rs553467008 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772790 | GGTGGTACGCATTTG[G/T]TATCCCAGCTACTTG | 27342 |
| rs553483848 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793756 | GCCATGAGTGCTTGG[C/T]CATTTTTACTGAGGG | 27342 |
| rs553495261 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776962 | CAGACTAACCTCTCC[A/G]AGTCCTGTCCACACT | 27342 |
| rs553496898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741567 | AATGTGTCGTGGGCG[C/T]CCGTGGGCTCGTTTT | 27342 |
| rs553555563 | in-del | -/TGACA | 0.00159617 | 0.0282053 | intron-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758414 | TTACTCTGTCTTCCC[-/TGACA]TAAGTGGGACCAATT | 27342 |
| rs553569898 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699152 | TTTCCTCGTGGGTCC[A/G]TTCTCTCCCCCGAGC | 27342 |
| rs553573310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693059 | TGAGCCGGCTGGTCC[C/T]GTGGCCTTCACTCAG | 27342 |
| rs553579684 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779298 | CACCTAAGGTCGGGA[A/G]TTCGAGACCAGACTG | 27342 |
| rs553590635 | in-del | -/TC | 0.00159744 | 0.0282165 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732764 | CGCTCTCTTGCTGTC[-/TC]TCTTTCTCACTCGCT | 27342 |
| rs553592913 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792673 | GCAAAACAAAGGCAG[A/T]CATTGCCTTTGCTCA | 27342 |
| rs553606882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746569 | GCTGCGATTACAGGC[A/G]TGAGCCACCGTGCCC | 27342 |
| rs553632093 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752973 | ATCTATTGAGCACCT[C/G]CTCAGTTCCTGGCAC | 27342 |
| rs553640063 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778551 | GTAGAATCTTGTGTA[C/G]CTCTTTCATGAACGG | 27342 |
| rs553662286 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722589 | TAAGAAAACCATTGC[C/T]TAATTCAAGGTCACA | 27342 |
| rs553664532 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785617 | CGGTGGCTCACGCCT[G/T]TAATCCCAACATTTT | 27342 |
| rs553674159 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744200 | AGGCGCGCGCCACCA[C/T]GCCCAGCTAATTACT | 27342 |
| rs553686206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694540 | AGCTAAAGAGGGGCA[C/T]GGTCAGGTTTGCATG | 27342 |
| rs553720564 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707614 | AATTGCTTGAACCTG[C/G]GAGGTGGAAGTTGCA | 27342 |
| rs553769487 | in-del | -/TTTTCTAATTTACCTTATGAT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706725 | AGCTGACTCAAAATA[-/TTTTCTAATTTACCTTATGAT]TTTTCTAATTTACCT | 27342 |
| rs553776123 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699588 | TCTTAGCTACTCGGG[A/G]GGCTGAGGCAGAAGA | 27342 |
| rs553780518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787454 | GTTCAAGCAATTTTT[A/G]TGCCCCAGCCTCCCG | 27342 |
| rs553808362 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704995 | AATAGATGAGGATTC[-/T]TGTACATGTTTTGTT | 27342 |
| rs553809192 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742714 | TGTGCTGAAGTGATC[A/C]TCCCACCTCAGCCTC | 27342 |
| rs553813213 | snp | A/G | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754000 | ATGAGCCAACGTACT[A/G]GGCCATTTTTTTTTT | 27342 |
| rs553818213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717425 | CTTATTTTTAAAATA[C/T]TTATTAGACAATATT | 27342 |
| rs553888647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706461 | CGTCCCCAGGCTGGA[A/G]TGCAGTGGTGTGATC | 27342 |
| rs553988329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688858 | AGCATTTTGGGAGGC[C/T]GAAGCGGGAGGATCA | 27342 |
| rs554008302 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774679 | GGATGAGAATTGCTT[G/T]AACTCGGGAGGCAGA | 27342 |
| rs554019984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712113 | TACAACCAGCTTGCA[C/T]ATGTCTACAAAAATC | 27342 |
| rs554060091 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759892 | ATAGGCATATAGTCC[C/G]TTTAAAACTGATCAC | 27342 |
| rs554062316 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689455 | AACCAAATGAAATGG[C/G]AAATCTCTAGAAACA | 27342 |
| rs554072292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724597 | TCTCGTGACCTTGTG[A/G]TCCACCCACCTCGGC | 27342 |
| rs554095270 | in-del | -/GT | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793798 | TGCTCCTGACCCCAA[-/GT]GTCCTGCCATCCTTT | 27342 |
| rs554126694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787405 | CTGTAGTGCAGTGGC[A/G]TGATTTCGGCTCACC | 27342 |
| rs554129783 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66682058 | GTCATCAGCCAAAGG[A/C]CCCGGAAGTGATGTT | 27342 |
| rs554142877 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767166 | TGCCACCATGCTCAG[C/G]TAATTTTTGTATGTT | 27342 |
| rs554143924 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692181 | CTGCCATACTGAACA[A/G]TCTGCATTGGCAGAT | 27342 |
| rs554150709 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694956 | AGCCCTGTTGAGGAC[A/G]AGGCTGGTGACCCAG | 27342 |
| rs554152278 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709231 | TCAGGCTGGTCTCGA[A/T]ATCCTGACCTCAGGT | 27342 |
| rs554162626 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749411 | CCATAAAGCTTTTGA[C/T]ATTGTTTTCTAAATG | 27342 |
| rs554190047 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786696 | GGTGTGAGCCACCGC[G/T]CCCAGTGCTATTCAG | 27342 |
| rs554203595 | in-del | -/AAAAAA | 0.499885 | 0.00758699 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739658 | CAGAGTGAGAGTCTC[-/AAAAAA]AAAAAAAAAAAAAAA | 27342 |
| rs554333904 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761175 | GTGTTGGGTTTCTTC[C/T]CCTACACACCACACC | 27342 |
| rs554336272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755070 | GAGGCCAAGGCAGGC[A/G]GATCACGAGGTCAGG | 27342 |
| rs554365957 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787078 | GTTGGCCAGGCTGGA[A/G]TGCAGTGGTGTGATC | 27342 |
| rs554384993 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787201 | CCAGATAATTTTTAC[-/T]TTTTTTTTTTTTTGT | 27342 |
| rs554404110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746856 | GGAGTGCAATAGTGC[A/G]ATCTTGGCTTACTAC | 27342 |
| rs554414845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765634 | TCTTGGGGTATGTCT[A/G]TTTCATTCTGTAGAC | 27342 |
| rs554428268 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716420 | GCCTGGGCAACGTGA[C/T]GAAAACCTGTCTCTA | 27342 |
| rs554461294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699267 | CATACATTCTTCTTT[C/T]TCTGCCTCATTCTCT | 27342 |
| rs554466918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732391 | ACCACCCACCAAGAG[A/G]TGAGGAGAAGCAGAT | 27342 |
| rs554500406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799191 | GCTCGTAGTACTTGC[A/G]GGGGTGATGTGTGTG | 27342 |
| rs554511858 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699117 | AACCTGTGGGGAGGC[A/G]AATTCCAGGCCCCTC | 27342 |
| rs554550647 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706030 | GCCTCAGCCTCCCGA[A/G]TAGCTGGGACTACAG | 27342 |
| rs554557917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719472 | CAGTGTGCTGGGATT[A/G]CAGGCATGAGCCACC | 27342 |
| rs554564236 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746998 | GGGGTTTCACCATGT[C/T]GGCCAGGCTGGTCTC | 27342 |
| rs554567370 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742201 | TGTACCAAGAAACTT[G/T]CCAGAGATGCAAGAA | 27342 |
| rs554572676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747235 | TGTGTTCATGAATGC[A/G]TAAAATATTACACAC | 27342 |
| rs554594812 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719027 | CAACAGGAATCCCTC[A/C]AGCACTCTTGGGGCC | 27342 |
| rs554607876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793164 | GAGCACTACAGGTTG[A/G]GTATCCCTTATCCGA | 27342 |
| rs554643712 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808365 | GGATTACAGGCGCCC[A/T]CAACTGCGCCCAGCT | 27342 |
| rs554685238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66753474 | CTTTGGAGATATTAC[A/G]GGTTTGGTTCTGCAC | 27342 |
| rs554698417 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712055 | TATTCTTATTCAAAT[A/T]TGCTTTGGCTATTCT | 27342 |
| rs554718392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726347 | GACCAGGAGGCCTCC[C/T]AGAGATTAGGAGGGA | 27342 |
| rs554735595 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718009 | TCTTCTATTTTCCTG[C/G]TGAGGGTTTCTATCA | 27342 |
| rs554775157 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681696 | TGGATCAAACGATTG[A/G]CTTAAGACCCTTTAA | 27342 |
| rs554819919 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694103 | CGTGAGCCACTGCAC[C/G]CAGCCTTGTTCGGTA | 27342 |
| rs554821395 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717318 | CATGTAGGTTCCTTT[A/C]CCCTGTCCTTACTAT | 27342 |
| rs554828124 | in-del | -/ATTA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701866 | GTCTGTGGTTTGTTT[-/ATTA]ATTTTTTTATTGATG | 27342 |
| rs554831719 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775505 | TTTTTGAGAACATCA[G/T]CTCAGATTTGACACT | 27342 |
| rs554861092 | snp | A/G | 4.9855e-05 | 0.0049925 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805438 | GGAGAAGGACTAGGA[A/G]GGTGGTGGTTTTGGG | 27342 |
| rs554873440 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686695 | GGATAAAGCTCCTAA[A/C]ATGCTGTAGGAAAAC | 27342 |
| rs554898288 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806002 | CTCCCACCTTGACCT[A/C]CCTAAGAGTTGGAAC | 27342 |
| rs554904486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687550 | TATGAGTGGTGGCAT[A/G]TTCCTGCAGTCCAAG | 27342 |
| rs554912563 | in-del | -/ATTC | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683729 | TACAAGGAGGTGCTT[-/ATTC]ATTTATTTATTTATT | 27342 |
| rs554919704 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733654 | AGTGAGCCAAGATCG[C/T]GCCACTGCACTCCAG | 27342 |
| rs554928967 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731131 | CTGGAGCCATGGCTG[C/G]GCCAGGTAAGGGGAA | 27342 |
| rs554931520 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708783 | TACCACTGTACTCTA[A/G]CCTGGGTGACAGAGC | 27342 |
| rs554936364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761985 | GAACCCGGGAGGTAG[C/T]GAAGGTTGCAGTGAG | 27342 |
| rs554941597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699552 | AAAAAATTAGCCGAG[C/T]GTCGTGGCAGGCACC | 27342 |
| rs554942832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723409 | TTTCACAATCTACCC[C/T]TACGTTGCGTTTAAC | 27342 |
| rs554955248 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755021 | CTCTGTTGGCCAGGC[A/G]CGGTGGCTCACACCT | 27342 |
| rs554961123 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781833 | CAAGTCAGCTAGGCT[C/G]TGTTTGAGTGGCCTC | 27342 |
| rs554984702 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801193 | TTAGGACAAGGAGAG[A/T]GTCAGGGCCTGTGGC | 27342 |
| rs554987628 | in-del | -/A/AAAAA | 0.00321478 | 0.0399632 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779671 | GCGAGACCCTGATTA[-/A/AAAAA]AAAAAAAAAAAAAAA | 27342 |
| rs555019823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66760997 | TAGCCCTGTTATTCT[A/G]TGGTCTCTACAATAA | 27342 |
| rs555068830 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682587 | TCGGTCCGGCTCCCA[C/T]TTCCCCGTCCAGGAT | 27342 |
| rs555072031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775932 | CTATTTTCCAGTGCA[C/T]GGATTTGTATGTAGG | 27342 |
| rs555092159 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66738937 | CCTCCTCAGCACAGG[G/T]ACTTTGTGTTTTTTT | 27342 |
| rs555106435 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738315 | TGAGCCACCATGCCC[C/G]GCCAGTCCTCTCTAG | 27342 |
| rs555130282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760605 | CATGCCATCATGCCC[A/G]GCTAATTTTTGTATT | 27342 |
| rs555150457 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773912 | CTCAAGTGATCCGGC[C/T]GCCTTGGCCTCCCAG | 27342 |
| rs555224173 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776529 | AAACCCCGCCTCTAC[-/A]AAAAAATAGAAAAAT | 27342 |
| rs555233422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743602 | CCCCTCCTGGGTTCA[C/T]GCCATTCTCCTGCCT | 27342 |
| rs555246104 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705696 | TGATAGATACAAGTG[G/T]TTTTTTTTTTGTTTT | 27342 |
| rs555252777 | in-del | -/AAAC | 0.00151783 | 0.0275066 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692066 | GTTTTCTTAAAAAAC[-/AAAC]AAACAAACAAACAAA | 27342 |
| rs555267883 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713237 | AGCTCTGCTTCCCGG[G/T]TTCATGCCATTCTTC | 27342 |
| rs555272499 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707552 | AACCAGCCAGTCGTG[C/G]TGGCACACACCTGTA | 27342 |
| rs555283977 | snp | C/T | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759977 | CACAAAATATCTAGA[C/T]AAGCTGGACAGTGTG | 27342 |
| rs555319325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776828 | CCAGAGATTAAATAA[A/G]AATGTATTGGGCTCA | 27342 |
| rs555327500 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784560 | CTCAGAATTAGCTCT[A/G]AAAGTTCCTTCTATG | 27342 |
| rs555346728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768348 | TCTTCTTTGTTAAAG[C/T]GTCTGTTGAGGTTTT | 27342 |
| rs555349225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742681 | ACACGATCACGAGTC[A/G]CTGAAGTCTCAACTG | 27342 |
| rs555363148 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795923 | GCAGGCGGATCACGT[G/T]AGGCCAGGAGTTCGA | 27342 |
| rs555363540 | snp | A/G | | | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66772078 | GGGAGCTGGCGGAGC[A/G]GTAAAAGGACTTAAC | 27342 |
| rs555373818 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RABGEF1 | GRCh38.p7 | 7:66809365 | ATTGGGATCTAGAAT[A/G]TAACTAAATTGCTTA | 27342 |
| rs555389221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783951 | AAAAATCCAGACCAA[A/G]AGATGTTAAATTACT | 27342 |
| rs555443054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689696 | CAATCCCAGCAACTC[A/G]GAGGCTGAGGCAGGA | 27342 |
| rs555478141 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695614 | CGTGAGAAAGTGAGG[C/G]ATTAGAAGTGTAGAT | 27342 |
| rs555491892 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757219 | TTAAAATGTTTTTCT[A/T]CAAGTGTTTACATAT | 27342 |
| rs555515595 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731296 | GGGAACCAGGAGGCC[C/T]TGGAAAACCAGAGAA | 27342 |
| rs555543949 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744443 | GGAGGCTGAGGCAGG[C/T]GGATCACGAGGTCAG | 27342 |
| rs555554164 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744662 | GACAGAGCCAGACTC[C/T]GTCTCAAAAAAAAAA | 27342 |
| rs555555353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756458 | TTTGCGGTCTGCTCA[A/G]GGTCATGGTCTGCTC | 27342 |
| rs555629934 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707031 | GCCTCGTGATCCACC[C/T]GCCTCGGCCTCCCAA | 27342 |
| rs555640942 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781732 | ATGTAGCCCTCTCCC[C/T]TCCGTAGTGTTTGCA | 27342 |
| rs555670102 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762736 | CCCGTCCCCCAAAAG[A/G]ATAATAATAAATAGG | 27342 |
| rs555701635 | in-del | -/C | 0.00874735 | 0.0655527 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749946 | ACCACTGCACTCCAG[-/C]GTGGGCGACAGAGCG | 27342 |
| rs555762831 | snp | C/T | 0 | 0 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740328 | AGGACTGAAACAGAG[C/T]TTCTGAAGCGTCCCT | 27342 |
| rs555823494 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727746 | CTGGGGAACCGTGAG[G/T]GGCAGGCTGCCCGTG | 27342 |
| rs555870012 | snp | A/G | 0.000519859 | 0.016114 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66775246 | CAGCGGGAGGAAGAA[A/G]AGGCCTTTGCCAGCA | 27342 |
| rs555870295 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744224 | AATTACTGCTATCTT[C/G]TATTTTAATTTTTTC | 27342 |
| rs555889458 | snp | C/G | | | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756294 | TAATGCTATGCTTAT[C/G]AGGTTATGGGAGACC | 27342 |
| rs555889887 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708846 | CAGAAAAATAGGTTT[G/T]GTTTTGTTTTGCTCT | 27342 |
| rs555897387 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748541 | GTCTGACAAGGGCAC[A/G]TATTTGTTTGTTTGT | 27342 |
| rs555899485 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742766 | TGCGTGCCACCACAC[C/G]CAGCTGATTTTTAAA | 27342 |
| rs555922631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715154 | TTCTCCTGAGACAGG[A/G]TCTCACTCTATCACC | 27342 |
| rs555926626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708323 | CAGGGTCTCACTCCA[A/G]TTTGCCCAAGCTGGA | 27342 |
| rs555973899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694615 | TGGAGGGGCAGGGCC[C/T]AGGAGCTAGTGACGT | 27342 |
| rs556010448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714705 | CTTTGGGAGGCCCAG[A/G]CGGGCGGATCATGAG | 27342 |
| rs556031302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737613 | GTGCTGTTCTCCTTT[A/G]ATTTTGCCAAGGAAA | 27342 |
| rs556051309 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701357 | AATTTAAAAAATTAG[C/G]CAGGCATGGTGGCGC | 27342 |
| rs556057878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707020 | TCGATCTCCTGGCCT[C/T]GTGATCCACCCGCCT | 27342 |
| rs556067096 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725839 | TGAGGGAGTTACACC[C/T]ATGCTTTGGAAAGTC | 27342 |
| rs556085411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688917 | AACCAACATGGCAAA[A/G]GCCCATTGCTACTAA | 27342 |
| rs556094078 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802707 | GGAACGGGTCTCTGC[A/G]GGATGAAGCATGTGG | 27342 |
| rs556104336 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810074 | TCATTCAGCAAATCT[C/G]TATTGAGTTCTTCAG | 27342 |
| rs556111494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702047 | CAATACCCATTAAGC[C/T]GTCACTCCCCAATCT | 27342 |
| rs556134931 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699294 | CTCTGTTCCCCTAGA[C/T]CGGGAGACAAAGGAC | 27342 |
| rs556140225 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701370 | AGCCAGGCATGGTGG[C/T]GCACACCAGTAGCCC | 27342 |
| rs556152430 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688401 | ACTTGAACAACATGA[C/T]AATCCAACTAGATCT | 27342 |
| rs556155433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695577 | AAAAGCCAGGCTGGA[A/G]AGAGTTTTGGAGAGA | 27342 |
| rs556168891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789599 | GAGGCAGGAGAATGG[C/T]GTGAACCCGGGAGGC | 27342 |
| rs556187500 | in-del | -/TTAT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735087 | CTAGAATTGTATTAC[-/TTAT]TTATGTAAGTTTTAA | 27342 |
| rs556195388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788911 | AGTTAGCCAAGGTCG[C/T]GCCATTGTACTCCAG | 27342 |
| rs556197225 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795937 | TTAGGCCAGGAGTTC[C/G]AGACCAGCCTGGCCA | 27342 |
| rs556219167 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | RABGEF1 | GRCh38.p7 | 7:66712193 | AAGCAGTGACATCCA[A/G]CCTGTATCAAGTCTT | 27342 |
| rs556221608 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714345 | CATTGTTAAATTTAT[G/T]ATATAGACTTGTTCA | 27342 |
| rs556241080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695107 | ACTTGAGATCAGAAG[A/G]TCAAGACCAGCCTGG | 27342 |
| rs556261518 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789126 | TCCTATACCTTAAAA[C/T]GACTCTATTGTTGTA | 27342 |
| rs556276307 | snp | A/G | | | utr-variant-3-prime | RABGEF1 | GRCh38.p7 | 7:66809341 | GGTAGCCCTTACTAC[A/G]CTCAACTGATTGGGA | 27342 |
| rs556277865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700389 | GATGAGGGAGTGACT[A/G]GAGGTCTCCCCGGAA | 27342 |
| rs556301533 | snp | C/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754637 | GCTGGATGTCATTTA[C/T]ATATGTGTCTTATAT | 27342 |
| rs556312153 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788172 | AAACTTGGGGCTGGG[C/T]GAGGTTGCTCACACC | 27342 |
| rs556344711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761952 | GTTACTTGGGAAGCC[A/G]AGGCAGGAGAATCAC | 27342 |
| rs556367356 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699697 | ATTCCATCTCAAAAA[A/C]AAAAAACAAAACTGG | 27342 |
| rs556410263 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761404 | GTGGTTTACAGAACT[C/G]AGGGAGATGCTTCTG | 27342 |
| rs556416453 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777543 | TTGGTGGTTTTAAAA[A/G]CCTGTGTCCCAAAAG | 27342 |
| rs556419695 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756308 | TGAGGTTATGGGAGA[C/G]CAGATTCCCTCATAC | 27342 |
| rs556422474 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787524 | AATTTTTTGTATGTT[G/T]AGTAGAGATGGGGTG | 27342 |
| rs556453726 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754399 | TTTAAAGCCATCATA[C/T]TTTAATATCTTTCAG | 27342 |
| rs556491501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793885 | TTGGCGTGTGAGGTC[A/G]GTGGCCTGTGTAGAT | 27342 |
| rs556535015 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715964 | TGGAGTGTTTTATCA[A/G]TATTAGTTGGTTTAT | 27342 |
| rs556556645 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715378 | TCAAGCAATCCTTTC[A/G]CCTTGGCCTCCCAAC | 27342 |
| rs556558484 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722371 | CTTGAACCTAGTAGA[C/T]GGAGGTTGCAGTGAG | 27342 |
| rs556588101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808509 | TTGAGGCACCGGGCC[C/T]GGTCTGGAGCTGTTC | 27342 |
| rs556595249 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721615 | CCTGCCTCCCCCCTT[A/G]TGAGAAACTTTGCAG | 27342 |
| rs556602448 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689625 | CTGGCCAACATGGTG[A/T]AATCCTGTCTCTACT | 27342 |
| rs556611190 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707750 | TGTTTATCTTCCCTC[C/G]AATTACTGCAGTTTT | 27342 |
| rs556618378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743878 | TCAAGTGATTCTCTA[A/G]CCTCGGCCTCCCAAA | 27342 |
| rs556637181 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811334 | AAGTCAGCATCAATA[C/T]AACGGCCGGAGTTTC | 27342 |
| rs556646164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713841 | TCAATGTGTTGGTAT[A/G]TTTTTCTTCTGTTAA | 27342 |
| rs556649590 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810863 | GTGGGTATAAAACTT[A/C]TTATTCTTAAATTTA | 27342 |
| rs556654264 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749657 | CTAGCCTGGGCAACA[A/C]AGCAAGACTCCATCT | 27342 |
| rs556677899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758068 | TTATCGTTTTACTAG[A/G]ATTGATTGGATGTTT | 27342 |
| rs556716362 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804139 | CCCAGGCTGGAGTGC[G/T]GTGGTATGATCGTAG | 27342 |
| rs556717391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66755871 | ATTGTATTCCAGGGA[A/G]TTGATTATCATTTGG | 27342 |
| rs556746314 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750578 | CTGTCTAGTAACTCA[A/G]TGCATTAAAAGATAC | 27342 |
| rs556786575 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696705 | AAAAAAAAAAAAAAA[A/G]AAAAAAAGAAAAATG | 27342 |
| rs556811828 | snp | A/G | 3.51636e-05 | 0.00419292 | utr-variant-3-prime | RABGEF1 | GRCh38.p7 | 7:66809290 | TGCAGGATGATCACA[A/G]TTTAGTGGAGAGTAT | 27342 |
| rs556823498 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696158 | GCAGCCTCAAACTCC[C/T]GGGCTCAAGCTATCC | 27342 |
| rs556848994 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719647 | TTCCCAAGTAATTTT[A/G]TGAGGCCAGTGTTAA | 27342 |
| rs556851214 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727223 | TGCTGACTAATGGAA[A/G]GTGGGGTGGACCTCA | 27342 |
| rs556857496 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734384 | GGTAAGATGCTCACC[C/G]TCTTTGAGCCTCTGT | 27342 |
| rs556866986 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788027 | CCTTGCTAAGTGTTA[A/G]TAAATCCCTCAGATA | 27342 |
| rs556909110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736333 | GTTCCTTTAGCAAAA[A/G]TCCTTTCACATATGA | 27342 |
| rs556922761 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776721 | GAAAAGAAAAAAGAT[G/T]GATTACATGATTAAT | 27342 |
| rs556927866 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765086 | GACATAATCACAGGT[A/G]TAGCACCAGAGAGTG | 27342 |
| rs556929447 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715308 | AATTTTTAAAAAAAT[G/T]TTTGTAGATACCGTG | 27342 |
| rs556942606 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66685466 | TGGAGACCAGCCTGG[A/G]CAACATAGCAAGACT | 27342 |
| rs556948545 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796708 | GTGATTCTCCTGTCT[C/G]AGCCCCCGAGTGGCT | 27342 |
| rs556951871 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766329 | AAAAAAGGAAGCTTA[G/T]TGCTTAGTGATGTCT | 27342 |
| rs556971117 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728641 | ATCCTCATCATCCTC[A/G]CCTCGACTTTCAGCT | 27342 |
| rs556985520 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680424 | TAATTTTGTATTTTT[A/T]GTAGAGACAGGGTTT | 27342 |
| rs557014380 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803528 | ACCCTTCGCTGTCCC[C/G]CAGGCTTGTTGGAAA | 27342 |
| rs557035451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686147 | TTAGCCAGGCATGGT[A/G]GTGTGTGCCTGTGAT | 27342 |
| rs557068239 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684440 | AGTGCAAGACTTCGT[C/T]TCAAACAAAACAAAA | 27342 |
| rs557080998 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66740944 | GCCTCCCGCTGTCCT[A/T]CGTCCCACATTCCGT | 27342 |
| rs557083758 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772164 | ACATTTTTTCACTTC[G/T]GCTTTGAGCTATCAG | 27342 |
| rs557093033 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740620 | CCTCCCGTCCAGAGT[A/C]AAAGGCCCCGGAAGT | 27342 |
| rs557143434 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778461 | AAGTCATAGTGGTTG[A/G]CCAAGCTGAGATACT | 27342 |
| rs557156747 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745332 | ATTTCTGGCATGTGG[G/T]TTTTTATTGGCTGCA | 27342 |
| rs557159764 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735830 | AATTAAACCTCTTTC[C/G]TTTATAAATCACCCA | 27342 |
| rs557175373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770645 | TACACCATCACTCCC[A/G]GCTAGTTGTTGTGTT | 27342 |
| rs557185719 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802164 | TCCCTAAGTTACTAG[A/G]ATTACAGGTGTGAGC | 27342 |
| rs557186764 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733830 | GAACATAGTGAAACC[C/T]CGTCTCTACCAAAAA | 27342 |
| rs557214742 | snp | C/T | | | intron-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811964 | GGGTGTTGTGGCTCA[C/T]GCCTGTAATCGCTTT | 27342 |
| rs557238759 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769544 | AAAAATAAGAGTGAG[G/T]TTAGAGGGGAGGGCT | 27342 |
| rs557241740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783156 | ACTTTGATCAGTATG[A/G]CTCACCAACGAAATG | 27342 |
| rs557277604 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740277 | TCGCCTTAAGACCTT[C/T]TAACTCGAACACCTG | 27342 |
| rs557296379 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720681 | TGCATTTAGCATAGT[A/G]CTAGAGGTTCAAGCT | 27342 |
| rs557322870 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785658 | GGCAGGCGGATCACA[A/G]GGTCAGGAGATAGAG | 27342 |
| rs557331057 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779287 | GGCAGGTGGATCACC[C/T]AAGGTCGGGAGTTCG | 27342 |
| rs557338926 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739725 | CAAGAACACTACAGC[A/G]ACAATTAGCAAAGCT | 27342 |
| rs557355519 | snp | C/T | | | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760686 | TGACCATGTGATCTG[C/T]CCGTCTCAGCCTCCC | 27342 |
| rs557390788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797609 | CCTTAAGGGAAAGCA[A/G]TAGCTCATGTTCCTG | 27342 |
| rs557405130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751817 | TTCCCTGTGTGGCTA[C/T]AGAATTTGGATTGTG | 27342 |
| rs557431518 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810797 | TTTTCCAGTATCTTC[C/G]TAAGGATGGAGCCCA | 27342 |
| rs557466800 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782406 | GAGTTATAAACACAT[A/G]TATTCTTATCCCACT | 27342 |
| rs557475984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733778 | GAGGCTGAGACGGGC[A/G]GATCATTTGAGGTCA | 27342 |
| rs557480296 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803837 | GAGGTTGCAGTGAGC[C/T]GAGATCGTGCCACTG | 27342 |
| rs557491287 | snp | C/T | 0 | 0 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745874 | CCAAAGTGGGAGAAT[C/T]GCTTGAGCCTAGGAG | 27342 |
| rs557493485 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704255 | CCTAACCAAAATTTA[A/G]CAGGTTATTTCTTAA | 27342 |
| rs557545163 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762609 | AGAAAAGAAAAAAAG[-/A]AAAAAAAAGAAATAG | 27342 |
| rs557570970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785531 | GATCACTAATCATAT[A/G]AATTTCTTGGGGCAG | 27342 |
| rs557588336 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690896 | GGAGACCAGCCTGGC[C/T]AACATGGTGAAACTC | 27342 |
| rs557591060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798287 | TGTGTACTCCAGTTG[C/T]GGTGGACACTGAGGA | 27342 |
| rs557625042 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696077 | AAAATATATATATAT[A/T]TTTTTCTTGAGTCAG | 27342 |
| rs557632431 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784748 | AAAAGCTTGCTTTCT[C/T]GCCCTTCAGAAATGT | 27342 |
| rs557635269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739597 | AACCTAGGAGGCGGA[A/G]GTTGCAGTAAGCCGA | 27342 |
| rs557692358 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686377 | TTTCGGAGGCCAAAG[C/T]GGGAGGATCGCTTGA | 27342 |
| rs557716445 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771536 | GTCATTGCAAAATCC[A/T]GTGTCGGGAAGCTTT | 27342 |
| rs557716975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783067 | TGGGATAGTGTAGTG[C/T]ATGTTTCCCTTGTCT | 27342 |
| rs557719099 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789466 | GATGGGCGGATCACA[A/G]GGTCAGGAGATCGAG | 27342 |
| rs557733243 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787681 | ACCTTAACCAAGCTT[C/T]ACACAGGTCTGAGAG | 27342 |
| rs557746368 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744110 | GGCATGATCTTGGCC[A/G]CTGCAACCTCTGCCT | 27342 |
| rs557752649 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752433 | CAGAAGGTGGAGGTT[A/G]CAGTGAGCCGAGATC | 27342 |
| rs557753108 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802874 | CAAAATGTCAACAGT[A/C]AAGATGAACAGGATG | 27342 |
| rs557753992 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721129 | TCACCAGGTTGGCCA[C/G]GCTGCTCTCGAACTC | 27342 |
| rs557786590 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728272 | ACATTAGCTAAGCTT[-/G]GGGGGGGCCACTGGG | 27342 |
| rs557811234 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774770 | GTCTCAAAAACAACC[-/A]AAAAAAGGATCCTAT | 27342 |
| rs557816452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684349 | CTCAGGAGGCTGAGG[C/T]AGGAGAATTACTTGA | 27342 |
| rs557848588 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735036 | TTATGAATGCTTTTC[A/C]AGAGGCTAAAAAGAA | 27342 |
| rs557859162 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769472 | AATCTTTAGTTAGGC[G/T]TCCACTCTGATCAGC | 27342 |
| rs557872010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745226 | TCAGTACTTACTCAT[C/T]GTGATGTCTACATAT | 27342 |
| rs557878013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723596 | TGTTTTTGTTTTTTT[C/T]TGAGACGGAGTCTCA | 27342 |
| rs557884175 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751717 | GACAGAGGTTTTATA[A/C]TGTCATATTTGTCTC | 27342 |
| rs557892863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689944 | TTAAAGGAAAATTAA[C/T]GCCAGTTTTTTGCAA | 27342 |
| rs557917649 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784693 | GCAGTGGACTTGTGT[C/T]AAAATAATTTTTAGA | 27342 |
| rs557950208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751171 | GAGTAGCTGGAATTA[C/T]AGACGTGCGCCACCG | 27342 |
| rs557951434 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740599 | CCTTTGGATCCACTC[C/G]CACTTCCTCCCGTCC | 27342 |
| rs557984510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790880 | GAGTTCATGAATCAC[A/G]CTGTATCTGCTCAGA | 27342 |
| rs557993447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782528 | CTGTGGAGTGTAGTG[A/G]GATGATCTCGTAGCT | 27342 |
| rs557998528 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750260 | TACCATCTATGAGAA[A/G]TTCAATGGCAAAGTG | 27342 |
| rs558012544 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739036 | GCTCACTGCAACCTC[C/T]GCTTCCCGGGCTCAA | 27342 |
| rs558031474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775507 | TTTGAGAACATCAGC[C/T]CAGATTTGACACTGA | 27342 |
| rs558075885 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743762 | CTCCTCGGCATTCCA[A/T]AGTGCTGGGATTACA | 27342 |
| rs558103471 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705166 | AACACTTTGGGAGGC[C/T]GAGGCAGGCATATCA | 27342 |
| rs558118623 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778356 | AGAGTTGGATACGCC[G/T]TCAGAGAAAGTAAAT | 27342 |
| rs558214895 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696856 | TGAATAAGCAAGTTA[G/T]TGGGCACAGATGACA | 27342 |
| rs558221886 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791868 | CCTGTAATCCCAGCT[C/T]TTTAGGAGGCCGAGG | 27342 |
| rs558223949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799008 | AACGCAGTAGGCAGC[A/G]AGGACAGGCAGCAGC | 27342 |
| rs558236357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798433 | ATTGGAAGTTTCATA[C/G]CTGAAGTGAGGAGTT | 27342 |
| rs558250257 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810508 | CTCCTGGTGGTTAAT[A/G]TGGTGTAACCAAAGA | 27342 |
| rs558274170 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740366 | GTAGCTCCGCTCCAC[C/G]TCCCATTCGCGCTAC | 27342 |
| rs558280167 | in-del | -/G | 0.00676609 | 0.0577691 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759651 | ATAGTGGAGAGCAAA[-/G]GGGGGAGCAAAGTGT | 27342 |
| rs558344829 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721863 | GCTTTGAAACAGAAA[G/T]TTTTTGGCCAAGTGG | 27342 |
| rs558357777 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702937 | AGGGTTTATTTTCAC[G/T]TTTTTGATAGTGTCT | 27342 |
| rs558390109 | in-del | -/TTTT | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66738946 | CACAGGTACTTTGTG[-/TTTT]TTTGTTTTGTTTTGT | 27342 |
| rs558396683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708916 | GGAGGGGGATAGGGA[A/G]AAAAAGAAATATGCA | 27342 |
| rs558402038 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716758 | TAGGTCTATCATTTT[A/G]TTATTTTCTGTTTGC | 27342 |
| rs558410876 | snp | C/T | 0.000947292 | 0.0217428 | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66797390 | GCCTCCAGAAAGAGT[C/T]GAGAAGATAATGGAT | 27342 |
| rs558434519 | snp | C/T | 1.64738e-05 | 0.00286995 | missense | RABGEF1 | GRCh38.p7 | 7:66805307 | AAGGGCAACCCCCCA[C/T]GCCTTCAGTCTAATA | 27342 |
| rs558444132 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66685556 | GTTTCTTTCTGTAAG[G/T]ATGTCTGACCCAGCT | 27342 |
| rs558460718 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714718 | AGGCGGGCGGATCAT[A/G]AGGTCAGGAGATCAT | 27342 |
| rs558482101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796571 | GCAGCCCAACAGTTG[A/G]AAGAAGATTTTTTTG | 27342 |
| rs558485434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764988 | GCTTTCATTGGGCCC[A/G]TCTAGATATCTAGCA | 27342 |
| rs558495179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803474 | GCAACCCCAGAGGTA[C/T]GCTGCCTCTCCAGCG | 27342 |
| rs558530678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711028 | AGCCAGGTATGATGG[C/T]GTGTACCTGTAGTCC | 27342 |
| rs558543112 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693106 | TCTAGAAGCCCTGAG[C/T]GGGCTTCTTCATGGA | 27342 |
| rs558544735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752762 | TACTCTGTGTTTTAA[C/T]TAGTCTTCCAAGTGA | 27342 |
| rs558558610 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691090 | GCGAGCCTCCATCTC[-/A]AAAAAAACAAAAAGA | 27342 |
| rs558572281 | in-del | -/CTC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684860 | CAGGATGGTCTCGAT[-/CTC]CTGACCTCGTGGTCT | 27342 |
| rs558584392 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724725 | TTCATGGTTTTCATC[A/C]AATTTATAGTTTGAA | 27342 |
| rs558614776 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717228 | GCTCTAAGAATTACA[G/T]TATGTACACCAAACT | 27342 |
| rs558646211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800120 | TTGTTCATGTAGACA[C/T]TGTTAATGAAATTCT | 27342 |
| rs558653894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759421 | TGTGTGAAGTGTTTT[C/T]TATTGTGAAAGCTCA | 27342 |
| rs558669043 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808219 | CTTCAGAGTTGTTCC[-/T]TTTTTTTTTTTTTCC | 27342 |
| rs558673816 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684695 | GCTGGAGTGCAGTGG[C/T]CTGATCTTGGCTCAC | 27342 |
| rs558674719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66753799 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGCAATTC | 27342 |
| rs558692644 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760033 | ACCCTTATCATATAG[A/C]GCATAGGGCTAGTAC | 27342 |
| rs558707504 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730431 | GAGTCTTGCTCTGTT[A/G]CCCAGGCTAGAGTGC | 27342 |
| rs558719971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752348 | AAAAATACAAAAATT[A/G]GCCAGGTATGGTGGC | 27342 |
| rs558771111 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705229 | AACATGGTAAAACCC[C/T]GTCTGTACTAAAAAT | 27342 |
| rs558774822 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699061 | AGCCGCATGGAGGAG[A/C]GGGGAGATATCTGGC | 27342 |
| rs558806106 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723331 | TTGCCATTTTGTCAC[A/C]TTTGACCCATTAGCT | 27342 |
| rs558809945 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702480 | GAACTCATGTTTTCA[A/G]TTCTCTTGGGTATAT | 27342 |
| rs558810842 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698423 | GTCAGAGGAGAGTGC[A/T]AGGTCCCCACCCACC | 27342 |
| rs558834353 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692978 | CCCATGCCGGAAGGG[C/G]CTGGCACCTCCCTGC | 27342 |
| rs558848428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729603 | TTCCACCTTTACCTT[C/T]ACCTTCACACCTGTC | 27342 |
| rs558850320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722768 | TTTTTCAAGATTGTT[C/T]TGTAATTCTGCATTT | 27342 |
| rs558878017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807414 | TTCCACAATTCCACT[A/G]CTTCCTTGTCTCTTT | 27342 |
| rs558910769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760461 | TTTTTTTTTTTTTTT[A/G]GAGACAGAGTCTCGC | 27342 |
| rs558934060 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693630 | AAGTTTTCCACACTT[A/C]CCAGTGCTCAGAAAC | 27342 |
| rs558937900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729053 | CCTCCTGGGTTCAAC[C/T]GATTCTCCTGCCTCA | 27342 |
| rs558982456 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682512 | TCTCCAGCGCCCGGC[A/C]GTGCCCCGACGGCCT | 27342 |
| rs559003008 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767087 | GGCTCACTGCAACCT[A/C]CATCTCCCCGGTTCA | 27342 |
| rs559003805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785952 | TGTTATTACCACCAA[C/T]TAAACTTTCTAGATG | 27342 |
| rs559021077 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66682101 | GTTACGGGCGTGCGC[G/T]GGCGGTGCCGGGGGG | 27342 |
| rs559040882 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740492 | AGGAAACGCCGGTTT[C/T]TCCGGGGCTCCCCAG | 27342 |
| rs559051447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730995 | CTAGTCTGAAATGAC[A/G]GCGCAGGGATTCGGG | 27342 |
| rs559058436 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715483 | CCCTTTAATTTGGCG[A/G]CATCGTGTAAGTTTT | 27342 |
| rs559067895 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693997 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 27342 |
| rs559069017 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766255 | TCAAGGCTGCAGTGA[C/G]CTGTGATCACGCCAC | 27342 |
| rs559077692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736934 | GACACCTACGTATAC[A/G]GACACACACACGTAC | 27342 |
| rs559078777 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743651 | GGACTACAGATGCCC[A/C/G]CCACCATGCCTGGCT | 27342 |
| rs559093913 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703104 | TCAGCCTCCCAAGTA[G/T]TTGGGACTATAGGCG | 27342 |
| rs559100850 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700003 | CGGGCTCCTCTGAGG[A/T]GCACCCAGAGACCCC | 27342 |
| rs559144574 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714935 | GCGAGACTCCGTCTC[A/C]AAAAAACAAAACAAA | 27342 |
| rs559182886 | snp | C/T | | | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756703 | TAACCTTAGATGACA[C/T]TCATCTCTTTAGAAC | 27342 |
| rs559184145 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692674 | GAGGCCCTGGTCATC[C/T]CTTCCCCACCCGCCT | 27342 |
| rs559185770 | snp | G/T | 0.00212089 | 0.0324953 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796782 | TTTTATTAGAGAGGA[G/T]ATTTCACCATGTTGG | 27342 |
| rs559187584 | in-del | -/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705490 | GAGAGAGAGAGAGGA[-/G]GGGGGAGGGGGAGGA | 27342 |
| rs559201553 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810918 | ACATCTGTGTCATCA[C/T]GCACTGAAGACAGGA | 27342 |
| rs559256381 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745486 | GTTATCACACCATAG[G/T]CTGGGTGCGGTGGCT | 27342 |
| rs559272569 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703638 | TTTTTTTCTGGAACT[C/T]TATTTCATTGGTCTA | 27342 |
| rs559276147 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742150 | AGCTAGACTCTATCT[C/T]AAAAAAAAAACTAAG | 27342 |
| rs559321255 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702467 | CAAGTTTTTGTGTGA[A/C]CTCATGTTTTCAGTT | 27342 |
| rs559323163 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692961 | TACCAGGCTCAAGGC[C/T]CCCCATGCCGGAAGG | 27342 |
| rs559351056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763153 | CAGGCGTGAGCCATT[A/G]CCCCTAGTCCACAGC | 27342 |
| rs559421387 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726593 | GGTCTGAAACTCCTG[C/T]TGGGCTCAAGTAATC | 27342 |
| rs559435648 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727884 | CTGCCTTGGAACACA[C/T]GCGTGGCTGCCTCTG | 27342 |
| rs559465169 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796224 | CATTTTGGTGAGTTA[C/T]TGTATTAATAGTTTA | 27342 |
| rs559467793 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729763 | ACGGAGAGGTGACCC[A/T]AGATGATGGATGGAT | 27342 |
| rs559506441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729313 | CTCCCCTCCATTCTT[C/T]GTTCCTCATCTCCAT | 27342 |
| rs559521832 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751230 | GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGCTG | 27342 |
| rs559555119 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734467 | ATTTGTATTTTTGTA[-/T]TTTTTTTTAGTAGAG | 27342 |
| rs559581059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757637 | TTCTTTTTGAGATGG[A/G]GTCTCGCTCTGCCGC | 27342 |
| rs559581126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750666 | AATGGTGCTTGAGAA[A/G]TAAGTTGAGATTATT | 27342 |
| rs559592657 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756759 | TTTCCATTTTCTGTT[G/T]GTCTCTAAAATCTTT | 27342 |
| rs559628365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734774 | AATGGGTGCATGATA[C/T]TGTTGTCATTTCTCG | 27342 |
| rs559735063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771710 | CAGGAATTTACTATA[C/T]TTAACATTCTTTTTT | 27342 |
| rs559743134 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807787 | GCCAGATGGTGTTCC[A/G]TTCTACTCAGATGAA | 27342 |
| rs559744020 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681369 | GACACTGGTTAATTA[C/T]TTCACTTCTGGGTCT | 27342 |
| rs559761968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686979 | GGCACCCACCACCAC[A/G]CCTGGCAAATTTTTT | 27342 |
| rs559778312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780057 | GGTTTTTTTTGTTTT[A/G]AAGCAAAAGTGTGTC | 27342 |
| rs559819066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730801 | GACCTCAAGTGATCC[C/T]CCTGCTTAGCCTCCC | 27342 |
| rs559839340 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779584 | GGCTGAGATGGGAGG[A/T]TCATTTGTGCCTGGG | 27342 |
| rs559852299 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716259 | TTGACCAGCATTTAC[A/G]TAACATATCTTTTTC | 27342 |
| rs559868221 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686215 | GAACCCAGTAGGTGG[A/G]GGTTGCAATGAGCCG | 27342 |
| rs559873570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772191 | TCAGCAAGTCAGTTT[A/G]ATATTAAGGAAAAGG | 27342 |
| rs559924203 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804725 | CTGGGCAACAAAGAG[G/T]GAAACTCAGTCTGAA | 27342 |
| rs559936054 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694174 | AGAAGGATCAGGCAC[A/G]TCCTTGCTCTCAAAG | 27342 |
| rs559954984 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66685854 | GGCACGTGGGGTTTT[A/G]TTGGCTGCAGAGCAA | 27342 |
| rs559979666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697482 | CTGCCCATCCCAGCC[A/G]CCAGCTCCCCTCCCT | 27342 |
| rs560003536 | snp | A/G | | | intron-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811613 | TTTGCTGTCACCACA[A/G]TCAATCAACCTTGTT | 27342 |
| rs560035663 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | RABGEF1 | GRCh38.p7 | 7:66740675 | TGCGTTCGCTGGCGG[C/T]GCCGGGGGCGGGGCG | 27342 |
| rs560044379 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752978 | TTGAGCACCTCCTCA[A/G]TTCCTGGCACTGTGC | 27342 |
| rs560079940 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766588 | GAGGAAGTAAACAGT[A/G]AACTTGAGAGTTTTT | 27342 |
| rs560085000 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700814 | GAGGCCTGGACACTC[C/T]CTGAGGACATCTCTG | 27342 |
| rs560108433 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741154 | CCACCTTCCGTCCAG[G/T]CCGCTGGCTCCGAAG | 27342 |
| rs560125285 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792598 | CCCTTTTCTCTTGAA[A/G]GAGGCACTATCTCTG | 27342 |
| rs560168958 | in-del | -/CT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707785 | TCATGTACTTTGAGG[-/CT]CTGTTTTTCGGTGCA | 27342 |
| rs560175063 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731298 | GAACCAGGAGGCCTT[C/G]GAAAACCAGAGAAGA | 27342 |
| rs560175808 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693818 | TTTTTTTTCTTTTTT[A/T]TTTTTTTGAGACAGG | 27342 |
| rs560207282 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706763 | TTCTAATTTACCTTC[G/T]TCTTTGACATACTGG | 27342 |
| rs560214842 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794060 | TGAACCCTGAATTAC[A/G]TAACTGTTTTCATCC | 27342 |
| rs560245347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743267 | GTGAGCCAAGATTGT[A/G]CCAATGCACTCCAGC | 27342 |
| rs560246736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741786 | ATCCTCCCGCCTCGG[C/T]CTCCCAGAGTGTTGG | 27342 |
| rs560249846 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712758 | GATTATAGGCGTGAG[C/G]CACTGCACCCAGCCT | 27342 |
| rs560251948 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706388 | TTAGTTTTTAAAAAC[C/G]CGCCAAACTGTTTTC | 27342 |
| rs560256131 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702461 | CATCTACAAGTTTTT[C/G]TGTGAACTCATGTTT | 27342 |
| rs560257786 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706179 | AGTCCTGGGATTATA[C/G]ACATGAGCCACCGTG | 27342 |
| rs560265694 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698757 | GTCTCAGTGTGGGTG[C/G]GTCTGACTCTGCCAC | 27342 |
| rs560268194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737070 | AGAGAGAGAGAGAGA[A/G]AGTGAGAGAGAGAGA | 27342 |
| rs560331325 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736696 | TGAAACCCCATCTCT[A/T]CTAAAAATACAAAAA | 27342 |
| rs560388643 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803184 | ACAGTAGCCTCATAA[C/G]TAAGGGAATAAAAGC | 27342 |
| rs560396650 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705332 | ATCCCACCTACTAGG[C/G]AGGCTGAGGCAGGAG | 27342 |
| rs560401038 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800769 | TACGGCCTGTTGCTA[A/G]TAGGGAAGTCCCCAG | 27342 |
| rs560422023 | snp | A/G | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680434 | TTTTTAGTAGAGACA[A/G]GGTTTCTCTCTGTTG | 27342 |
| rs560447254 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770408 | CCATACAGCTGTGAG[A/T]CTGAACAAATGAGTT | 27342 |
| rs560448157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793587 | GCAAATGAAAGGTGT[A/G]AAACCATGTGTAAAC | 27342 |
| rs560453192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737918 | GCCCAGATATTTGCA[C/T]AGCAGCACAGCTGGC | 27342 |
| rs560455736 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807021 | GTTCTTTATCCAAAG[C/T]GAGTCAGACAACCTG | 27342 |
| rs560464434 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704798 | CCTGGGTGACAAAGT[C/G]AGACTCCGTCTCAAA | 27342 |
| rs560465265 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711383 | TTAGTCTTACATTTA[A/G]ATCTGAGATCTTTTT | 27342 |
| rs560503037 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746500 | TTCACCATATTGGCC[-/A]GGCTGATCTCGAACT | 27342 |
| rs560509666 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694710 | AATGAAGTCGGAATC[C/T]CGTGGATTGGCCTTG | 27342 |
| rs560539980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719099 | GGTTACCCAACTGCT[C/T]TTGCTTGTCTCACCA | 27342 |
| rs560545541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700026 | GAGACCCCAACTCAG[A/G]GGAGGCAGTGCAAAC | 27342 |
| rs560549837 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783383 | GTTCATGATTGAATA[G/T]ATAGATCAAAGTGTG | 27342 |
| rs560551795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698515 | GTTTGGAGCAGGAGC[C/T]CGGGTCTGGACGATG | 27342 |
| rs560596831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748174 | GTCGAGTTTTACTTT[A/G]TGTGTTAGTAAAACT | 27342 |
| rs560605054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807870 | ACTGTTTCCCAGGCT[A/G]GTCTGAACTCCTGGT | 27342 |
| rs560659882 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754554 | TTGGAGACCAGCCTG[A/G]CCAACAGGGTGAGAC | 27342 |
| rs560664169 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747658 | ACAGAGGAAATTTAA[A/C]TTCTTAAAATTAGAA | 27342 |
| rs560676531 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66753994 | ACAGGCATGAGCCAA[C/T]GTACTAGGCCATTTT | 27342 |
| rs560679289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697645 | TATTCTTGGCCTCAC[C/T]ATTCACTGAGGATTA | 27342 |
| rs560694367 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750818 | TCAGTGAAATGCAAA[G/T]ATTTCAGTTTCATTC | 27342 |
| rs560709334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730006 | AAAGAAATCAGGAAA[C/T]TCCAGTAGGAGGGAA | 27342 |
| rs560720650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66685333 | TAATTACTTCTGTCT[C/T]GTATTTTAATCTTCT | 27342 |
| rs560731904 | in-del | -/TTC | | | cds-indel, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810657 | ATATACCATTGATGA[-/TTC]TTCTTCCATTCAGTG | 27342 |
| rs560761550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772442 | TGGCACTCATCAAGC[A/G]TTATTTCCCTCATTC | 27342 |
| rs560774092 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778997 | GTGTGCGCCTGTAAT[C/G]CCAGCTACTTGGGAG | 27342 |
| rs560783299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792043 | CTTGAACCTGGGAGG[C/T]GTAGGTTGCAGTGAA | 27342 |
| rs560812025 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760186 | TCCTTCCCCTCCTCT[G/T]CCTTGCCTTCGACAC | 27342 |
| rs560900824 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742520 | CTGCATGTGTCTTGA[A/C]GAATGACTAACATTC | 27342 |
| rs561003899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741034 | GCGGCCTCTCCGTCC[C/T]AGACGCTAGTTGCCG | 27342 |
| rs561015980 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | RABGEF1 | GRCh38.p7 | 7:66740733 | CTGGCCGCGGAGCCC[A/T]GACCTACCCGGGCGA | 27342 |
| rs561053024 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752046 | AACAAACCAAAAAAA[A/C]CCCGCAAAAAACTAG | 27342 |
| rs561081355 | in-del | -/C | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741715 | ATTTATTATTTTTTT[-/C]GACATGGGATCTCAC | 27342 |
| rs561085708 | snp | C/G | | | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756965 | GTTCTTGTGTTCACA[C/G]TCTTCTAACTAGTTT | 27342 |
| rs561086090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711660 | GGCACAATCTCGGCT[C/T]GCTGCAAGCTCCGCC | 27342 |
| rs561089285 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746138 | ACAGTTATCCCACTT[A/C]ATATTATTTAACTTA | 27342 |
| rs561117868 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716812 | GAGACAAGGTCTTGC[C/T]CTGTTGCCCGGGCTG | 27342 |
| rs561119008 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806981 | AACATACACTTGCCT[A/G]CGAGGGAAGAGCGTT | 27342 |
| rs561122940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717610 | GTCACCCAGGCTGGA[A/G]TGCAGTAGTACAATC | 27342 |
| rs561144853 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706844 | TGGACTGCAGTTTCG[C/T]GATCTCAGCTCACTG | 27342 |
| rs561152031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752364 | GCCAGGTATGGTGGC[A/G]GGCACCTGTAATCCC | 27342 |
| rs561161066 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793979 | CATCCTTATGAGAAC[C/G]GTTGGGAGAAATTTT | 27342 |
| rs561164060 | snp | C/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739490 | GAAACCCTGTCTCGA[C/T]TAAAAATACAAAAAA | 27342 |
| rs561178183 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735279 | CTTTGTAGCCTATTC[C/G]AACCGTGTGTATCCC | 27342 |
| rs561178303 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777173 | AGAATACTCATTCCT[A/G]TTTAGCTTAAGGTCT | 27342 |
| rs561200940 | in-del | -/AC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736936 | CACCTACGTATACAG[-/AC]ACACACACGTACACA | 27342 |
| rs561231705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806443 | CCAGCATTGTGTTCA[A/G]CTACATGTTACTGTA | 27342 |
| rs561251144 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747138 | AGCATAGCTCTCTTG[A/G]CAATGGTCATTAAGA | 27342 |
| rs561300142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724788 | TACTCCAATTATATG[C/T]GTGTTGGATGGATTA | 27342 |
| rs561325024 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734249 | AGAGGCACGGGTTAT[C/T]GGTGTCTGATGGAGG | 27342 |
| rs561340995 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755289 | ACAGAGTGAGACTCT[A/G]TCTCAAAAAAAAAAC | 27342 |
| rs561346870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747540 | GCTAAAATTAAAAAT[C/T]GCTTTTGGGGGATTT | 27342 |
| rs561347278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761488 | GGGGGCGAGGAATGG[A/G]GGAAGGTGCAGAACT | 27342 |
| rs561356876 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755354 | GTGATGCACACCTGT[A/G]GTCCCAGCTACTTGG | 27342 |
| rs561408763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760873 | ACTTTGAGCCATCCT[C/T]CCACCTTCGCCTCCC | 27342 |
| rs561443036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800197 | GCCATCGAGTAGGCT[C/T]CTTTTGTTACAGGAA | 27342 |
| rs561471623 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759671 | GAGCAAAGTGTCTCC[A/C]CTAGTGGGAGCAGGA | 27342 |
| rs561516666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724392 | TTGAGACGGAGTCTC[A/G]CTCTGTCACCAGGTT | 27342 |
| rs561574337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683186 | TCTCACAATGTTACC[C/T]AGGCAGGTGTCAAAC | 27342 |
| rs561587243 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703084 | GTTCACTCCATTCTC[A/C]TGCCTCAGCCTCCCA | 27342 |
| rs561604700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686932 | GTTCAAGCCATTCTC[C/T]TGCCTCAGCCTCCCG | 27342 |
| rs561627116 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730563 | TTTCTTTTTCTTTTT[C/T]TTTTTTTTTTTTGGT | 27342 |
| rs561650339 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700626 | TGGAGAAAAGGGGTT[C/T]GTGCGTAGCAGGGGG | 27342 |
| rs561686088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737394 | GAATAGCTGGGACTA[C/T]AGGCGTGTGCCACCA | 27342 |
| rs561697331 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686779 | GAAGTGACTGTCAGT[A/G]GGATAGGAAGTCTAA | 27342 |
| rs561718170 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691015 | AGAATCGCCGGAACC[A/G]GGGAGGCAGGGGTTG | 27342 |
| rs561727329 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719320 | TGGTTTACCATCTTA[C/G]CCTCCTGAGTAGTTG | 27342 |
| rs561745654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689033 | GGGAGAGGGAGGTTG[C/T]AGTGAGCCGAGATTG | 27342 |
| rs561798286 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783320 | TATTTGTTGACTAGT[C/T]TTATAAACTCCAGCA | 27342 |
| rs561803072 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767257 | ATCCACCCGCCTCAG[C/G]CTCCCAAAGTGCTGG | 27342 |
| rs561804326 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682708 | CAGCCCCCGGCCGCG[A/G]CAGGGCGCCGGGATT | 27342 |
| rs561831414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688471 | ACACATTCTTTTCAA[A/G]AGCATGTGGGACATT | 27342 |
| rs561867605 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694688 | AAGCCAGTGGCAGTA[C/G]GGAGAGAATGAAGTC | 27342 |
| rs561871910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742812 | TTGTCTTGCTGTGTT[A/G]CCCTGGCTGATCTCA | 27342 |
| rs561906796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732147 | AGGCCACCGCCCTCT[C/T]TTCCTATGGTCCAGG | 27342 |
| rs561961957 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789021 | TTAAAGCTTTGTACC[C/T]GAATGAGGACAAAAA | 27342 |
| rs561978109 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780287 | GCTTTGGATTTAAGC[A/G]CACAGACCTGGGTTC | 27342 |
| rs561986498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787614 | CCTCCCAATGTGCCG[A/G]GATTACAGGATTGAG | 27342 |
| rs562044294 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719358 | TAGGTGCACGCCACC[A/G]AGCCCAGCTAATTTT | 27342 |
| rs562049059 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733975 | GTGCCATTGCACTCC[A/T]GCCTGGGCGACACAG | 27342 |
| rs562070313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66755939 | TTTGTTATATTTAAC[A/G]TTAAAACTCTGACAT | 27342 |
| rs562084462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683928 | AAAGATTTTGTAAAG[A/G]TGTTGTCTTGCTGCG | 27342 |
| rs562096180 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682678 | CGCCGGGATGGGACG[C/G]TCGGACCCAGACCAC | 27342 |
| rs562140487 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739823 | CACGTTACGCCATAC[A/G]TGGCATTCAGGACGC | 27342 |
| rs562153367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768726 | TCAGATCCATGCATA[C/T]GCAGCCTAGGGGTAA | 27342 |
| rs562157244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749724 | CACCTGTAATCTCAG[C/T]ACTTTGGGAGGCCAA | 27342 |
| rs562181757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789012 | TATATGGACTTAAAG[C/T]TTTGTACCTGAATGA | 27342 |
| rs562213948 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765202 | AGGAAAGGGAGTTTC[A/G]GAAATATTACATAGT | 27342 |
| rs562262945 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764951 | TGGGCCCTTGTTATC[C/T]TCTGCATTTTAGAGT | 27342 |
| rs562321392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714037 | GACTTCTGTTTTTGT[A/G]CTACCATAGTCTAGT | 27342 |
| rs562321717 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743492 | CTACTAATTTAGCTT[G/T]CCTGGCTAAATTTTT | 27342 |
| rs562323918 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700989 | GGCAGCGCTGTCTTG[A/C]AGCCCAAGGAAGCCG | 27342 |
| rs562360614 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707371 | TTCTGTTTTTTTTCT[C/G]ATCTGATATCTAGTT | 27342 |
| rs562363603 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742451 | CGAGGAAGGAGCCGG[C/G]CATTTAGGCCATGCT | 27342 |
| rs562378190 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802007 | CTTGACCTCACAGGC[C/T]CAAGCGATCCGTCCG | 27342 |
| rs562390357 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760201 | TCCTTGCCTTCGACA[C/T]TCTTAACCTGGAAAA | 27342 |
| rs562394136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688315 | GAAAAGAAGAGTTTC[A/G]CAGTGATCATTGGTG | 27342 |
| rs562405404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788632 | GAAGCAGTTAAGCAC[A/G]ACATAACACCTTTTG | 27342 |
| rs562407447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795007 | TGGTCATGGTGAGAC[C/T]GCTAGGTGGGAAGGG | 27342 |
| rs562410353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732123 | GGTAGCTAGAACGCC[C/T]GGCTCACCAGGCCAC | 27342 |
| rs562426287 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807141 | ACTGACAGTAGAGGT[A/G]GCTGGCTTGCACACA | 27342 |
| rs562430313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749001 | GGCTCTTGGTAGGTG[A/G]TATCAGGCCTTCAGG | 27342 |
| rs562447633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718615 | AAGCTGCAACTTCCT[A/G]CCTGCACTCCGTGAG | 27342 |
| rs562474901 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808028 | TGTATTCATTGCTCG[C/T]TGCAGGCCTCTCGGA | 27342 |
| rs562478427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741859 | AGAGTGTGTTCCGGC[C/T]GGGTGCGGTGGCTCA | 27342 |
| rs562487539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760838 | CTTGCTGTGTTGCCC[A/G]GGCTGGTCTTGAACG | 27342 |
| rs562492954 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773153 | ATTTGTAGTGAACTC[A/G]GAGAATTAGAAATTA | 27342 |
| rs562496608 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780043 | TACATTTTAAAAGGG[-/T]TTTTTTTTGTTTTAA | 27342 |
| rs562530603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687564 | TGTTCCTGCAGTCCA[A/G]GCTACTCAGGCAGTT | 27342 |
| rs562542691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695360 | TGAGATCTGAGGGCC[A/G]CTCACATGAAAGGGA | 27342 |
| rs562555115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806604 | AAAAAAGTTTAAGTG[A/G]CCCATATAGAATGAG | 27342 |
| rs562563479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736817 | AGTGAGCCAAGTTTG[C/T]GCCACTGCACTCCAG | 27342 |
| rs562624129 | in-del | -/T | 0.0119091 | 0.0762411 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794261 | AAAAAAATTTTTTAA[-/T]TTCTTTCTTTCTCTT | 27342 |
| rs562624287 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751008 | TTGAAATTCTTAATC[-/T]TTTTATGTTTTCCCT | 27342 |
| rs562626059 | snp | C/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755766 | CCAAGGAGAGCGTGA[C/T]CTAGTACAATAGAAG | 27342 |
| rs562631609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700977 | TTCAGTGTGGTGGGC[A/G]GCGCTGTCTTGCAGC | 27342 |
| rs562661756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737205 | AAAATGCTGGTATTA[C/T]AGTATTTATTTAATT | 27342 |
| rs562662220 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788598 | TTAATAGTCATTCTG[A/C]TAAGCTCTTCTTTCT | 27342 |
| rs562668144 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700169 | CTGCACATTCCAGCC[C/T]TGGTTCATTCTGGAT | 27342 |
| rs562677681 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694258 | AAGTAAAGGGTGCCA[C/T]GGGAATGGGAAAGAT | 27342 |
| rs562680689 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684306 | AAAATTAGATGGGCA[C/T]GATGGCGCCTACCTG | 27342 |
| rs562683456 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699317 | CAAAGGACTGGATTT[C/G]AATCCTGTCTTTGCC | 27342 |
| rs562685541 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754150 | GGACTACAGGCGCCC[-/T]TCCAACACGCCTGGC | 27342 |
| rs562716902 | in-del | -/AGAAA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778003 | TTAAAAATTCATGTT[-/AGAAA]AGAAGATTCCATTGT | 27342 |
| rs562719838 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775536 | GAAATTGGGCTTGAG[A/G]GTCAGACAGTATATG | 27342 |
| rs562749075 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757443 | ATAGTCATATCTCTC[-/AT]ATTACACACTAAGCT | 27342 |
| rs562768384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706189 | TTATAGACATGAGCC[A/G]CCGTGCCCGGCCTGT | 27342 |
| rs562775406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787832 | GTTAACCTTTCCCAT[A/G]ATAACTAGAAAACCA | 27342 |
| rs562785645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782611 | CAAATAGCTGGCACT[A/G]TAGGTATGCACTACC | 27342 |
| rs562795237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786855 | CAAGATATTTCCATT[A/G]CAAATGAGACGGGCA | 27342 |
| rs562798922 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705453 | AAAGAAAGAGAGAGA[G/T]AGAGAGAGAGAGAGA | 27342 |
| rs562831464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739204 | ATCTGCCCGCCTCGG[C/T]TTCCCAAAGTGCTAG | 27342 |
| rs562849408 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768078 | TACTATAACCGTTTG[A/C]GTATAGAATTTTGTA | 27342 |
| rs562882029 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775026 | CAGTAGCTGAATGAG[A/T]ATGAGAAGACCCCAT | 27342 |
| rs562883666 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791156 | CTAGCTGCTAAAAAT[G/T]ACGGATTTCTGGCTT | 27342 |
| rs562891368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732723 | TCGCTCACTCTCTCT[C/T]GCTCTCTCTCTCTTG | 27342 |
| rs562924229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738430 | TCTTCTGCTCAGCCC[A/G]TTGAACACTCATTCT | 27342 |
| rs562940026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748895 | GAAACCCTCACAGAG[C/T]TTTCTGTCACCCTGG | 27342 |
| rs562943636 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744323 | GGATTGCTTGAGGTC[A/G]GGGGTTGGAGACCAG | 27342 |
| rs562956679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781971 | TCCAGTGTCTGAAAA[C/T]CTTTTGTTCATATTT | 27342 |
| rs562958216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713307 | CCACCATGCCCAGCT[A/G]ATTTTTTGTATTTTT | 27342 |
| rs563000834 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714850 | TGAGGCAGGAGAATG[G/T]TGTGAACCCGGGAGG | 27342 |
| rs563036657 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801403 | GAATCCTGTTATATT[A/C]TCTTAATTACTTTTT | 27342 |
| rs563072070 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742994 | AGGGGAAGTTTTTTA[C/G]CTGGGTCCTTGTGTG | 27342 |
| rs563085699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721147 | TGCTCTCGAACTCCC[A/G]AGCTCAAGTGATCTG | 27342 |
| rs563110331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706821 | GAGTCTTGCTCTGTC[A/G]CCCAGGCTGGACTGC | 27342 |
| rs563117888 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810387 | TGCCAGTAGCACCCC[C/T]GCTAGAGCTGTGAAA | 27342 |
| rs563119366 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720592 | AAAACTTAAAGCTAA[A/T]ATTTTAATGGATAAA | 27342 |
| rs563151393 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708482 | TAGTAGAGACGGGGT[G/T]TCACCATGTTGGGTC | 27342 |
| rs563169670 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754727 | GCCATCTAACAAATC[G/T]GAATAAATACATTTC | 27342 |
| rs563204067 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800762 | TAGCCTTTACGGCCT[C/G]TTGCTAATAGGGAAG | 27342 |
| rs563209828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756591 | GTCCCTTATTTGCTT[C/T]TATATTTTGGCTACA | 27342 |
| rs563214773 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743409 | AGCTCACTGTAGCCT[C/G]CACCACCCATGCTTA | 27342 |
| rs563225602 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736697 | GAAACCCCATCTCTA[C/T]TAAAAATACAAAAAT | 27342 |
| rs563229309 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66809707 | AGATAGAAATTATAT[G/T]GATAAGTAAATATGT | 27342 |
| rs563244716 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802991 | AAGGCTAAAGATAAA[C/T]GAAGGTAGTAAAAAT | 27342 |
| rs563286309 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752372 | TGGTGGCGGGCACCT[A/G]TAATCCCAGCTACTG | 27342 |
| rs563305116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789870 | TGGTGTTGGCATTGT[C/T]TCCCAGCCTTCTCAG | 27342 |
| rs563324346 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721300 | TGTATATTAGTGTCT[C/T]ACTGCTACTCTAACA | 27342 |
| rs563351531 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708015 | TTTTAATCCATTCTG[C/G]CAATCTGTGCCTTTT | 27342 |
| rs563386960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683913 | ACCCAGCTGATTTTT[A/G]AAGATTTTGTAAAGA | 27342 |
| rs563401410 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727575 | AGAGATGAGATGTTT[G/T]GTTCTCTGAGCAGGA | 27342 |
| rs563408414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795761 | AGTGCCTTTGAACTG[C/T]ACCATGCGTATCTTT | 27342 |
| rs563411284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689991 | GAAGAGGAGGAAATA[C/T]TTTCTAACTCATTCT | 27342 |
| rs563426787 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783603 | TAAATAACCTTAGGT[A/G]AGATACTTAAAGTAA | 27342 |
| rs563456746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763060 | TGGAGTTCAGTGGTG[C/T]AGTCATAGCTCGCTG | 27342 |
| rs563472012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802256 | AGTGGGTAGAGGCCA[A/G]GGATTCTACTAAACA | 27342 |
| rs563477520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762388 | TTGAGGCCAGGAATT[C/T]GAGATCAGCCTGGTC | 27342 |
| rs563507328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804648 | GCTGAGGCAAGAGAA[C/T]CGCTTGAACCCAGGA | 27342 |
| rs563542339 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768692 | GTTCCAATTTGGAAG[A/C]CTTTGGTACGGAATA | 27342 |
| rs563580217 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680141 | ATCTTTAAAGTAAAT[A/G]TTATTGTCTTTTGGT | 27342 |
| rs563610113 | in-del | -/TCT | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729381 | CTTCCATTCTCACTC[-/TCT]TCTCACTCACTGTCC | 27342 |
| rs563631463 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728397 | CCCCTATGGCTGGGT[C/G]AGCTTCGAGGTTCAT | 27342 |
| rs563649609 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722813 | GAATCAGCGTGTCAC[G/T]TTCTACAACAGGCAG | 27342 |
| rs563650042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715672 | CAGAAAGCATCGTTT[A/G]TATAATTTTAAATTA | 27342 |
| rs563659962 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738496 | GCACTTTTGGAGGCC[A/G]GGGTGGGCAGATTGC | 27342 |
| rs563662861 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680752 | AGGAGTACTAGACTA[G/T]ACTGGCCAATATGAT | 27342 |
| rs563676703 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740041 | TTCAGTGGAGGGATC[C/T]CTGCACCGTCAACTT | 27342 |
| rs563702944 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699712 | AAAAAAACAAAACTG[A/G]TGTGGTAGTGTGCAC | 27342 |
| rs563708775 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771008 | GTTATTGAGTTGTAG[C/G]AGTTCCTTCGTATTT | 27342 |
| rs563736011 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749746 | GGAGGCCAAGGCGGG[A/C]GGATCACGAGGTCAG | 27342 |
| rs563737761 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722104 | CAAGGTTTCAGGGAG[A/C]CATGATTGTTTCACT | 27342 |
| rs563748054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692505 | CCCAAAACCATCACC[A/G]TGAAGGAGCTGAGGG | 27342 |
| rs563767527 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729214 | CTCGGCCTCCCAAAG[G/T]GCTGGGATTACAGGT | 27342 |
| rs563772069 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769296 | GATGAAATCTGTGAG[A/G]CCTCTCTCCCCAGCA | 27342 |
| rs563817917 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811098 | TTTTAGGTGTGAATC[C/T]AGATATGCGGTCTTA | 27342 |
| rs563854475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702367 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 27342 |
| rs563875964 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696946 | AACAGCTGGCCATGG[G/T]GGATGGGGAGCAAGA | 27342 |
| rs563877022 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715989 | GTTTATGATTGTGTT[G/T]AGTTCCATATCCTAG | 27342 |
| rs563884946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727558 | GGACCCAGCTTGGGT[A/G]GAGAGATGAGATGTT | 27342 |
| rs563920312 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726769 | AACCCTTTGGGAGGC[C/T]GAGGTGGGCTGATCA | 27342 |
| rs563929554 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784234 | TCTGTTTTGTTTTTT[A/G]TATTTTGATTTTGAA | 27342 |
| rs563933874 | snp | C/G/T | 0.000143482 | 0.0084688 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756033 | TACAGATTGCAAATG[C/G/T]TAATAAGTCTTTTAT | 27342 |
| rs563946052 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714086 | TTGGCTTTATACAAC[A/C/G]ATTTTGGAAGTGTTC | 27342 |
| rs563961848 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696460 | TTTGAGAGGCCAAGG[C/G]AGGTGGATCACTCGA | 27342 |
| rs563982869 | snp | A/T | 0.103438 | 0.202533 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720509 | ACCCCACTGATAATT[A/T]AAAAAAAAAAAAATC | 27342 |
| rs564008725 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732604 | CAGTCTCCCCAGAGT[C/G]CAGGCAGCCCTCTAT | 27342 |
| rs564014346 | snp | A/C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772450 | ATCAAGCATTATTTC[A/C/T]CTCATTCTTTTAATA | 27342 |
| rs564034836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708990 | TCTACTTGATTCTGC[A/G]TCAGTAGTATGACCT | 27342 |
| rs564037503 | snp | G/T | 4.94295e-05 | 0.00497115 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795622 | CATTGAGAGATTGCG[G/T]GTATTGCACAGGGAT | 27342 |
| rs564059197 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692382 | TTCTGCACCTACAGC[A/G]TTGTCTTAAGGTAAG | 27342 |
| rs564059986 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716797 | GTTTGTTTGAGACAG[C/G]AGACAAGGTCTTGCT | 27342 |
| rs564062686 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757651 | GAGTCTCGCTCTGCC[A/G]CCCAGGCTGGAGTGC | 27342 |
| rs564068800 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66809508 | CATTTAAGGCTTGTG[C/T]GCAAATTTTGTCTCA | 27342 |
| rs564159820 | in-del | -/CACTCACAGTCTTCAT | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807317 | GACGAACCCCACGGG[-/CACTCACAGTCTTCAT]CACTCACAGTCTTCA | 27342 |
| rs564166332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713403 | AAAGTGCTGGGATTA[C/T]AGGCTTGAGCCACTG | 27342 |
| rs564179198 | in-del | -/TTTTA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747617 | AATACATAGTGAAAG[-/TTTTA]TTTTTGTAGTTCCTC | 27342 |
| rs564180141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684690 | GCCAGGCTGGAGTGC[A/G]GTGGCCTGATCTTGG | 27342 |
| rs564187122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683842 | ACTGCCTGGGCTCAA[A/G]TGAACCTCCCACCTC | 27342 |
| rs564198227 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769786 | CAATCCAGACTCTGT[A/T]GCTTAGAGTTTTAAA | 27342 |
| rs564210801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801795 | GACACCCTTTCCCAT[C/T]TGGCTCCACCTGCAT | 27342 |
| rs564246941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781861 | CTCTCCCTGTGCCAA[A/G]ACTTTAAAACTCTCC | 27342 |
| rs564257946 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768456 | GTTCTTTGCCAAATA[G/T]GTGATTTGCTGCAAG | 27342 |
| rs564333359 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774917 | AGCAGCTGTCCCATT[A/C]TGTAGCAGTTGTTTA | 27342 |
| rs564360397 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744279 | GGCTCACGCCTGTAA[C/T]CCTCGCACTTTGGGA | 27342 |
| rs564363110 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684900 | TCGGCCTTCCAAAGT[A/G]TTGGGATTACAGGCG | 27342 |
| rs564394965 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774406 | TCTTTCTTGCTTCCC[C/T]ACCACATGATGAAAT | 27342 |
| rs564409057 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691250 | ACCTCCCATACCGTA[C/G/T]ATAATTCTATATATT | 27342 |
| rs564429132 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734032 | CAAAAAAAACCTCCT[A/G]GAGGCAGTCATCAGC | 27342 |
| rs564450524 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706149 | CCTCATGATCCACCC[A/G]CCTCGGCCTCGCAAA | 27342 |
| rs564473131 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750314 | CTGATGCTTTTTATA[A/G]AACATTGTTAAGGTG | 27342 |
| rs564479975 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739993 | ATGTTTTTTTTGAGA[C/G]AGGATCTCGCTCTGC | 27342 |
| rs564493339 | in-del | -/TCTTC | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772221 | GATGTTTTCCTCTCT[-/TCTTC]TCAGTCAGCTTTTAA | 27342 |
| rs564548968 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803862 | CCACTGTACTCTAGC[C/T]GGGGCAACAGAGTGA | 27342 |
| rs564551247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697583 | GACCATGATTCATGC[C/T]CTTCCAGCAGGCTTC | 27342 |
| rs564568523 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763909 | TTTGGGTTGTTTCTG[C/T]TCTTGGACTATTATG | 27342 |
| rs564572893 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734576 | GCTGAGATTACAGGC[A/G]TGAGCCACCATGCCT | 27342 |
| rs564576490 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805942 | GAGAGATGGGGTCTC[A/G/T]CTGTGTTGCCCAGGC | 27342 |
| rs564615208 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789814 | TCATCCTGGGGCAGC[C/T]GTGGTGGCTCCATGC | 27342 |
| rs564657540 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792078 | GATCACGCCACTGCA[C/G]TGCAGCCTGGCGACA | 27342 |
| rs564673169 | in-del | -/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810185 | AGCTGTGAGATGCAA[-/G]GGGCGCCTTGCAGCC | 27342 |
| rs564683770 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735409 | TCAAACTGGCAGAGA[G/T]CCACATAAGACCTTT | 27342 |
| rs564722891 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739429 | GGAAGCCAAGGTGGG[A/C]GGATCACTTGAGGTC | 27342 |
| rs564727141 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime | RABGEF1 | GRCh38.p7 | 7:66740723 | GAGGCGGGAGCTGGC[C/T]GCGGAGCCCAGACCT | 27342 |
| rs564735161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699584 | GTAATCTTAGCTACT[C/T]GGGAGGCTGAGGCAG | 27342 |
| rs564749891 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | RABGEF1 | GRCh38.p7 | 7:66740725 | GGCGGGAGCTGGCCG[C/T]GGAGCCCAGACCTAC | 27342 |
| rs564769015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708356 | GCAGTGGCGCAATCT[C/T]GGCTCACTGCAACCT | 27342 |
| rs564851249 | in-del | -/TA | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686868 | CCCTGTTGCCCAGGC[-/TA]TATAGTGCAGTGGCG | 27342 |
| rs564870327 | snp | C/T | 0.0119091 | 0.0762411 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66682011 | GCACCCTACTCTGTG[C/T]AAGCCTTTGGATCCC | 27342 |
| rs564887818 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759324 | TTCTACAGGACACCA[A/G]CATTGTTAAGATTCG | 27342 |
| rs564911501 | in-del | -/AGAGTC | 0.00716266 | 0.059414 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698405 | GGCAGCCCACGAAAG[-/AGAGTC]AGAGGAGAGTGCAAG | 27342 |
| rs564919686 | in-del | -/AATA | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716602 | AAGACTCTGTCTCAG[-/AATA]AATAAATAAATAAAT | 27342 |
| rs564925143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785657 | AGGCAGGCGGATCAC[A/G]AGGTCAGGAGATAGA | 27342 |
| rs564992532 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715622 | TTGAATATTTTTTAG[A/T]GTTCTATTATTGACT | 27342 |
| rs565027772 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709632 | TCTCTACTAAAAATA[C/T]GAAATTAGCCAGGCA | 27342 |
| rs565038122 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689719 | AGGCAGGAGAATCAC[C/T]TGAACCCGGGAGGCG | 27342 |
| rs565081812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751283 | TGATCCGCCTGCCTC[A/G]GCCTCCCAAAGTGTT | 27342 |
| rs565100134 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758207 | CACATCTGCAAAGTA[G/T]TTTCGTTTTGCTTTT | 27342 |
| rs565108297 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757911 | CCACTGCGCCCGGCC[A/G]ACCAAAACATTTTTT | 27342 |
| rs565108434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716295 | TTAAACTTATAATCT[A/G]CCTATATTAAAATAT | 27342 |
| rs565118033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723699 | GATTCTCCTGCCTCA[A/G]CCTCCTGAGTAGCTG | 27342 |
| rs565166416 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804410 | TTCTTCCTTCTCCAT[G/T]GAGCTCAGAGGCAGC | 27342 |
| rs565188448 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710848 | GTTCATACCTGTAAT[C/T]GCACCATTTTGGGAG | 27342 |
| rs565207540 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734016 | TCTCAAAAACAAAAA[A/G]CAAAAAAAACCTCCT | 27342 |
| rs565225154 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721869 | AAACAGAAAGTTTTT[G/T]GCCAAGTGGGGTGGC | 27342 |
| rs565238669 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66753653 | TCCAGTGGATGTCTT[C/T]GCATAACAGTGTTTT | 27342 |
| rs565241635 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729394 | TCTCTTCTCACTCAC[C/T]GTCCCTCTTTCACCT | 27342 |
| rs565293347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66753064 | AGTATTATAATGGCT[A/G]TATTTATAAAAAGCT | 27342 |
| rs565297359 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711480 | AACAATATCCAATAT[G/T]CCAGCACCATTTGTT | 27342 |
| rs565299210 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775601 | TTTTAGAGAAATTTG[C/T]TTATAGGAGGAATCA | 27342 |
| rs565331718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734233 | GACCTGGGAGGCAAG[A/G]AGAGGCACGGGTTAT | 27342 |
| rs565334259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717564 | GAGTTCAAGACCAGC[C/T]TGGCCAGTATGGTGA | 27342 |
| rs565350280 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759605 | AACATTGCAGCTTCT[G/T]CTTCTAGGGTGGCCT | 27342 |
| rs565353900 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740091 | CTCCCACCTCAGCCT[C/T]CCTGGTAGTTGGGAC | 27342 |
| rs565370212 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733663 | AGATCGTGCCACTGC[A/C]CTCCAGACTGGGCTA | 27342 |
| rs565375236 | snp | A/G | 8.25852e-05 | 0.0064254 | missense | RABGEF1 | GRCh38.p7 | 7:66799366 | CTGTGTGTCCCTGTT[A/G]ATGAAGACATCCCAG | 27342 |
| rs565387636 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798768 | CAGGAGTTTGAGACC[A/C]GCCTGGCCAGCAGGG | 27342 |
| rs565389018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806248 | AAGTCTCACAGGTAC[A/G]TGAATCTCTCAGTCT | 27342 |
| rs565393893 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681822 | CGCTTCCACCGTGGC[C/T]TCGGCTCCAGGAGTC | 27342 |
| rs565467579 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739585 | GAGAATCGCTTGAAC[C/T]TAGGAGGCGGAGGTT | 27342 |
| rs565499059 | snp | C/G | | | intron-variant, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66685590 | TTGTAAACAGGAATT[C/G]TGCACTCATTTCTGT | 27342 |
| rs565523989 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765252 | CAGTACGTGGCAGAG[C/T]TGGGGTTGGAGTGCA | 27342 |
| rs565525438 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786904 | AATCCTTTTATGTTG[A/C]AAATATAGTTGCCAT | 27342 |
| rs565537912 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772358 | AGTGGAAGAATGGAG[A/T]TAGGCATATTTCCTG | 27342 |
| rs565558038 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708139 | TCTTCCATTATAGCC[C/G]TCCTTTTATGTTCTG | 27342 |
| rs565597518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771805 | ATAATGGAATCACTC[A/G]CTTTTTGTTCATAAT | 27342 |
| rs565643218 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696076 | AAAATATATATATAT[-/A]TTTTTTCTTGAGTCA | 27342 |
| rs565648939 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691541 | GTGACTTACAATGGT[G/T]TGACTTGGGATTTTT | 27342 |
| rs565653935 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740185 | GCTCTGTGGCCCAGG[A/C]TGGTCTCGAACTCCT | 27342 |
| rs565669744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701802 | CTATTTATAGATTCT[A/G]GATACAAGTTCTTTA | 27342 |
| rs565674653 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802456 | TCTGTGTTTCCTATT[A/C]ATGTGAAGGCAGAGC | 27342 |
| rs565687746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690812 | TATAAGGCCAGGTGC[A/G]GTGCCTCACCCCTAA | 27342 |
| rs565699317 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742100 | AGGTTGCAGTGAGCC[A/G]AAATCGTGCCACTGC | 27342 |
| rs565702354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789350 | AAATAGCTCTGAGCT[C/T]TCAGCATCTATAAGT | 27342 |
| rs565716310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776445 | AGCCTGTAATCTCAG[C/T]GCTTTGGGAGGCCAA | 27342 |
| rs565740662 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749861 | CGCCTGTAGTCCCAG[A/C]TACTCGGGAGGCTGA | 27342 |
| rs565767979 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789977 | CAGATACTCCCTCTA[C/T]GGACAAGATACTCAT | 27342 |
| rs565830156 | snp | C/G/T | 1.66427e-05 | 0.00288462 | intron-variant, missense | RABGEF1 | GRCh38.p7 | 7:66783705 | AAGCTCCCAGTCCTT[C/G/T]CATAAACCGGCAAAC | 27342 |
| rs565947606 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756210 | TCTAAAGATGGCTAA[C/G]CTTAGGGAAATGCAC | 27342 |
| rs565948320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745207 | AAAAAAAAAAAAAAT[A/G]ATATCAGTACTTACT | 27342 |
| rs565964560 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703426 | TACAATTTTAGCTCT[C/G]ACAGTTAGGTCTTTT | 27342 |
| rs565979335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757228 | TTTTCTACAAGTGTT[C/T]ACATATTGATGCTAT | 27342 |
| rs566003895 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728467 | TCTGCTTGTTCCTGT[G/T]CCCACCATAACCATG | 27342 |
| rs566029633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791340 | TAATGACCTCAAGAT[A/G]TACTCCCTGGTGAGA | 27342 |
| rs566086354 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806600 | ACTGAAAAAAGTTTA[A/T]GTGGCCCATATAGAA | 27342 |
| rs566137603 | snp | G/T | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759880 | AAACCATATCACATA[G/T]GCATATAGTCCCTTT | 27342 |
| rs566147246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805904 | CATGCACCATCACAC[C/T]GGGCCAATTTTTTTT | 27342 |
| rs566171674 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681525 | CACCTCAGCCTCCCC[A/G]GTAGTTGGGACCACA | 27342 |
| rs566202909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763320 | CCTTCCAGATGCACT[C/T]GTGTTGGCAGAATTC | 27342 |
| rs566211112 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721420 | ACAGATTCGCCTTCT[A/G]GAGGCTCTTGGGGGA | 27342 |
| rs566222225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715804 | GCTGGAGTGCAGTGG[C/T]TATTCCCAGCACAAT | 27342 |
| rs566245876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722187 | TGGCTCACGCCTGTA[A/G]TCCCAGCACTCTGGG | 27342 |
| rs566252801 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728024 | TAGACCCAATGTCCC[A/C]CTTCCACCTTTCCAG | 27342 |
| rs566260301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715247 | ATTCTCCTGCTTTAG[C/T]CTCCCGAGTAGCTGG | 27342 |
| rs566293461 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803355 | ATACCCCACCGCCTG[G/T]CCAGAGTCTGAAACG | 27342 |
| rs566296863 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686041 | CCCAACACTTTGGGA[A/G]GCTGAGGTGGGCAGA | 27342 |
| rs566346401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811670 | CTTCAAACAGACATA[A/G]AAGTAGAGAAAAAAG | 27342 |
| rs566356699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684838 | ACGGGGGTTTCACCA[C/T]GTTAGCCAGGATGGT | 27342 |
| rs566365627 | snp | A/G | 6.93565e-05 | 0.00588842 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66772073 | GGACTGGGAGCTGGC[A/G]GAGCGGTAAAAGGAC | 27342 |
| rs566365693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779192 | ACAAAAATCATAATC[C/T]GTGTGTTAATTTAGT | 27342 |
| rs566426999 | snp | A/T | 0.0501905 | 0.150254 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778282 | TACGTAGCAGCTTGG[A/T]AGCAGACAAAATACA | 27342 |
| rs566447013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717026 | TCAGGTGATCCGCCC[A/G]CCTCAGCCTCCCAAA | 27342 |
| rs566510779 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759384 | GATGTGCTTACTTCC[C/G]CAGCCGTAAACTCTA | 27342 |
| rs566521638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731681 | ATGATTGTGCCACTG[C/T]ACTCCAGCCTGGGTG | 27342 |
| rs566530738 | snp | C/T | 0.0748431 | 0.178382 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723811 | TCTCGAACTCCTGAC[C/T]TCAGGTGATCTGCCC | 27342 |
| rs566557324 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730947 | AGAACTGGCAGGGGT[C/G]GGGTGGATTCGGGGA | 27342 |
| rs566581595 | in-del | -/G | 0.00636936 | 0.0560724 | utr-variant-5-prime, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66682110 | TGCGCTGGCGGTGCC[-/G]GGGGGGGCGGGGCAA | 27342 |
| rs566601693 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715506 | TAAGTTTTGACATGT[C/T]CTATTTTCATTTTCA | 27342 |
| rs566625077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736210 | CCCCCTAGGTCTTCA[C/T]CCATGCACACACTTT | 27342 |
| rs566642184 | in-del | -/A | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690721 | ATAAAATAAATAAAT[-/A]AATATTTTAAAAAAT | 27342 |
| rs566690852 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735604 | ATCATTGTGGGGGGG[G/T]TTTCCCCTTTGGTGC | 27342 |
| rs566705955 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744249 | TTTTTCTGCTTATTA[G/T]ATGTTTGAAATGGTG | 27342 |
| rs566744682 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797846 | TCAAGGCAGGGGATG[C/T]CGGCTGGGCCCGGTG | 27342 |
| rs566747411 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705700 | AGATACAAGTGTTTT[C/T]TTTTTTGTTTTTTTT | 27342 |
| rs566753830 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697667 | TGAGGATTAGCAGGG[C/T]GGGGGTAGCTGGGGC | 27342 |
| rs566761703 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785258 | ACCTGCATATGGCCT[C/G]AGATTCCTCCTGTTT | 27342 |
| rs566763180 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694444 | CGGAACATAAGGTCT[A/G]GCTGGAAAGGTGGGA | 27342 |
| rs566784606 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705122 | AAAGCAATAGATGGC[C/T]GGGCGCGGTGGCTCA | 27342 |
| rs566788065 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66740835 | AGCTGCTCGGCTCTC[A/G]GCTACAGGAGCGGGG | 27342 |
| rs566805567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704053 | TTGATTTTGAAGCTA[C/T]TGCACATAGAATGGC | 27342 |
| rs566816397 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795323 | ACTAAGGAAAAGTCC[A/G]GCAACAATGGATATT | 27342 |
| rs566844541 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687973 | GCCTGTAATCCCAGC[G/T]ACACGGTAGGCTGAG | 27342 |
| rs566851654 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699462 | TTGGGAGGTCGAGGC[A/G]GATGGACCACCTGAG | 27342 |
| rs566855931 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767855 | TACCCAGTTTATGGT[A/G]TTTTGTTACTGCAGC | 27342 |
| rs566857503 | in-del | -/A | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739499 | CTCGACTAAAAATAC[-/A]AAAAAAAAAAATATG | 27342 |
| rs566868387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799625 | AGGGATTATGGTCTC[A/G]TTTCTTGGGCATTAA | 27342 |
| rs566868814 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710989 | CACTACAAAAAAAAA[A/T]TAATAAAGGAAATAA | 27342 |
| rs566883181 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687370 | AACTGAGGTGATCCA[A/T]CCTCCTCGGCCTCCC | 27342 |
| rs566897130 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781053 | TGATTTTTGATAAGG[A/G]AAGGTTTACCCCTGC | 27342 |
| rs566905820 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773854 | TATTTTATGTAGAGA[A/C]AGGGTTTCACCATGT | 27342 |
| rs566923077 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758017 | GGAAAAAAATCACCC[A/G/T]TAAGTTTTATTTCTT | 27342 |
| rs566935736 | snp | A/G | | | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756254 | TTTTGTTTGCCTGTC[A/G]GATTGACAAAAAATT | 27342 |
| rs566953011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693978 | ACGTTTGGTTAATTT[C/T]TTGTATTTTTAGTAG | 27342 |
| rs566968604 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780341 | GTGACTGCAACATTA[A/T]TCAAGTTACTTAACA | 27342 |
| rs567012407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692880 | GGCTCCTGGCACCTA[C/T]ATCCTGGCTGGACCC | 27342 |
| rs567021444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786460 | CTGGACTGGAGCACA[A/G]TAGCGCAGTTGCTGC | 27342 |
| rs567048105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742001 | AAAAAGAAAAAGAAA[A/G]TTTGCCGGGCATCGT | 27342 |
| rs567051666 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811337 | TCAGCATCAATACAA[C/T]GGCCGGAGTTTCTGT | 27342 |
| rs567097043 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725580 | AGTTTTGATGAGTTC[A/G]TGAATATTGTGATGT | 27342 |
| rs567138149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746578 | ACAGGCGTGAGCCAC[C/T]GTGCCCGGCAGGAAG | 27342 |
| rs567140726 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697185 | GAAGGCAAGAGGAGG[A/C]CTGGGCTCCAGCCCA | 27342 |
| rs567168267 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745837 | CAGTGGCTCATGCCT[A/G]TAATACCAGTGCTTT | 27342 |
| rs567205703 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66809953 | TATATAGTCAGAGAC[A/T]ATGACACCACTAAGG | 27342 |
| rs567239742 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723209 | CTTGACCTCATGTTA[A/T]CTGCCTGCCTCAGCC | 27342 |
| rs567246073 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66685467 | GGAGACCAGCCTGGG[A/C]AACATAGCAAGACTG | 27342 |
| rs567247046 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758614 | TGAGTCTCACGCAGC[C/T]GATCCCCCATGTTTC | 27342 |
| rs567253792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734999 | AGGAAGTTTCAGGAA[C/T]GTTAAGGAAGTTAAG | 27342 |
| rs567262230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686024 | TGGCTCACGCCTGTA[A/G]TCCCAACACTTTGGG | 27342 |
| rs567262358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728704 | ATCATCCTCACCTCA[A/G]CTTTCAGCTCTGTCC | 27342 |
| rs567264715 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771392 | TATCCGCCCTCCTCA[A/G]CCTCCCAAAGGGCTG | 27342 |
| rs567307380 | snp | A/G | 0.000665203 | 0.0182252 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66771941 | AATTCATGTGGATCA[A/G]TCGGATCTCCTGTGC | 27342 |
| rs567308721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764843 | CCTTGTGCCAGTACC[A/G]CGCTGTAGTAATTAC | 27342 |
| rs567337417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741916 | CCAAGGCAGGCGGAT[C/T]ATGACGTCAGGAGCT | 27342 |
| rs567347903 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734909 | CACCCCACAAAACTG[C/G]TCACCACATGGCCAA | 27342 |
| rs567370796 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778261 | TAAAGGAAAGTTTTT[A/G]TGCCATACGTAGCAG | 27342 |
| rs567374601 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713719 | AAAAGAGTTTTTATT[G/T]AGCATGGATGTTGAA | 27342 |
| rs567376464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777632 | GTACTTTAAAAAGAA[A/G]CATTTCTGGAGCTGG | 27342 |
| rs567405167 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687685 | TTAGTTAAATAAAAT[-/A]AAACATGATCCATCT | 27342 |
| rs567406434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735536 | CCTGCCCAAATCTCA[C/T]GTCAAATTGTAATCC | 27342 |
| rs567460568 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737167 | GCTCCTGGCTTTAGG[C/T]AATCCTCCCACCTTG | 27342 |
| rs567482392 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740590 | CCGCTCGACCCTTTG[A/G]ATCCACTCGCACTTC | 27342 |
| rs567490035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702673 | TATAGTCATCTTCAT[A/G]GGTATGAAGTGGTGT | 27342 |
| rs567498241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710918 | GAGGCCAAGACAGGA[A/G]GATCACTTGAGGCCA | 27342 |
| rs567568193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698993 | AAGCTGAGTCCAGCC[C/T]GTCCTTCAGTCCCAC | 27342 |
| rs567576703 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745107 | TGAGGCAGGAGAATG[G/T]CGTGAACCCGGGAGG | 27342 |
| rs567579819 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772756 | TCTACTAAAAATATT[A/T]AAAAAGTTAGCCGGG | 27342 |
| rs567584473 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716976 | TAGAGACGGGGTTTC[C/G]CCATGTTGGCCAGGC | 27342 |
| rs567593266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709198 | ATTTTTAGTAGAAAT[A/G]GAGTTTCACCATGTT | 27342 |
| rs567593533 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740290 | TTTTAACTCGAACAC[C/T]TGTCACATCCTAGGA | 27342 |
| rs567608334 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705606 | TATAATTGCTTCAAT[G/T]ATCTTTTAGAGCCAT | 27342 |
| rs567666300 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805734 | TAAGGCTGAATATTT[G/T]CCCCCTCATTCATTC | 27342 |
| rs567666495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716544 | AGGCAGAGGTTGCAG[C/T]GAGCCAAGATGGCAC | 27342 |
| rs567681486 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693446 | AGGGTGAGAAGGTAG[G/T]TCTCATGCCCCTCCC | 27342 |
| rs567682659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787433 | ACCCCAACCTCTGCC[C/T]CCCAGGTTCAAGCAA | 27342 |
| rs567689788 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779774 | AACTGTAACGTGGAT[G/T]AGGTTGTTCTTTTCC | 27342 |
| rs567723616 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754744 | AATAAATACATTTCA[C/G]GTCTAGGCATTGCGT | 27342 |
| rs567742669 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798797 | GGTGAAACCCTGTCT[C/T]GTAAAAGTACAGAAA | 27342 |
| rs567768097 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745887 | ATCGCTTGAGCCTAG[A/G]AGTTCCAGGCTGCAG | 27342 |
| rs567773480 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785880 | CTCCATCTGGGGGGG[A/G]AAAAAAAAAAGTCTT | 27342 |
| rs567783850 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704266 | TTTAACAGGTTATTT[A/C]TTAATTAACCACTCT | 27342 |
| rs567784637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754166 | TCCAACACGCCTGGC[C/T]AATTTTTTTGTATTT | 27342 |
| rs567789250 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705030 | GTATACCTAAGTATT[G/T]CATTTTTGGGAGAGC | 27342 |
| rs567836533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746454 | CACCATACCCAGCTA[A/G]TTTTTTTTGTATTTT | 27342 |
| rs567839156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791589 | TAGAATGTGGCAATT[C/T]ACATTGAAATGATGG | 27342 |
| rs567881570 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697092 | TCCCTCTGTGTCAAC[C/G]AGGAAGCACAGTCAT | 27342 |
| rs567892786 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66753621 | TTTCAGTTTGAAGAG[C/G]TCTCCCTGGTATTTC | 27342 |
| rs567928447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759247 | TTTATTCCTTGCTAT[A/G]GTTTGTTACAGTGAG | 27342 |
| rs567953767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759871 | CACAGTTCCAAACCA[C/T]ATCACATAGGCATAT | 27342 |
| rs567980339 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680717 | TTTGGGAGACCAAGG[C/G]AGGTGGATGATTTGA | 27342 |
| rs568039663 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742702 | GTCTCAACTGCCTGT[C/G]CTGAAGTGATCCTCC | 27342 |
| rs568040209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800923 | GCTGTGTTCCATGAA[C/T]AGTGGGACTCGATAG | 27342 |
| rs568053772 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747873 | AGAAAGGGTTTGTAA[A/T]GACTTACAAAGATAC | 27342 |
| rs568068161 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706449 | GGAGTCTCGCTCCGT[A/C]CCCAGGCTGGAGTGC | 27342 |
| rs568084951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713081 | CAGCTTCCCAAAGTG[C/T]TGGGATTATAGGCAT | 27342 |
| rs568121299 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721877 | AGTTTTTGGCCAAGT[C/G]GGGTGGCTTATGCCT | 27342 |
| rs568123059 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793804 | TGACCCCAAGTGTCC[G/T]GCCATCCTTTTAGAG | 27342 |
| rs568123493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712529 | AGGCTGGAGTGCAGT[A/G]TCGTGATCACAGCCC | 27342 |
| rs568134129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682424 | AGCGCCGCCTGCCCC[A/G]TTTCAGGCCGCCCTC | 27342 |
| rs568149965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725198 | TTTACAGCTTTATCA[A/G]GATACACTTTACTTT | 27342 |
| rs568164275 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789824 | GCAGCCGTGGTGGCT[C/G]CATGCGTGAGGCTGG | 27342 |
| rs568193783 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711760 | CCCGGCTAATTTTTT[A/G]TATTTTTAGTAGAGA | 27342 |
| rs568208934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689337 | AAAAAGAAAACTCAA[A/G]TAGCCAAAATCAGAA | 27342 |
| rs568217949 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773741 | TGCAATTTCAACTTA[C/T]TGCAACCTCTGCTTC | 27342 |
| rs568224666 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781517 | TATCCCTCCCCTTGT[A/C]CCCCACCACCCAATA | 27342 |
| rs568238618 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731486 | GTTTGGGAGGCCACC[A/G]CAGGTGGATCACTTA | 27342 |
| rs568245736 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695449 | GGGCAGGGGCTTTGA[C/T]GCAAGAGGTTCCACA | 27342 |
| rs568249117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718021 | CTGCTGAGGGTTTCT[A/G]TCATTCCATTCATTT | 27342 |
| rs568254185 | snp | C/G | 0.00716266 | 0.059414 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66682048 | ACTTCCTCCCGTCAT[C/G]AGCCAAAGGCCCCGG | 27342 |
| rs568284350 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688722 | ATGAATAAAAATGAA[A/C]ACACAACATACCAGA | 27342 |
| rs568324283 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694845 | AATGAGGGGAACAAC[A/G]GGGCTGGGGGATCAG | 27342 |
| rs568350257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720259 | TTGGAGTGCAGTGGC[A/G]CGATCTCGGCTCACT | 27342 |
| rs568355898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687266 | AGTAGGTGGGATTAC[A/C]GGCATGCACCACCAT | 27342 |
| rs568370260 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683457 | AATGACCTTTCCAAT[C/G]AGTCAGTTTCTGCTC | 27342 |
| rs568414046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788098 | TAAAGGGGGCAGGCT[C/G]TACTTCCTCAAAGTA | 27342 |
| rs568426083 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780615 | CTTTTTAAAAATCAC[C/G]TCTCTGTCAATTACT | 27342 |
| rs568443867 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755725 | GGAGAATGGCATGCT[C/G]AGATTAGAGTTACAA | 27342 |
| rs568456121 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785058 | ATAGCATGTATGCTG[G/T]ATAATATGTTTTAGA | 27342 |
| rs568484294 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793146 | GAGTTTCTAGTTGGA[A/C]GCGAGCACTACAGGT | 27342 |
| rs568521402 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682957 | AGGTCATAGGCAGCT[A/G]GCGGTGTCTCAGCGC | 27342 |
| rs568527138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761041 | GTTTTTCTTCTTTCA[A/G]CAAAGAATTGAGAAC | 27342 |
| rs568549550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726503 | CAAGTAGCTGAGACT[A/G]CAGGTATGCACCACC | 27342 |
| rs568560809 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742415 | ACAGTGTGGTAAGGA[A/G]TGTGAGCTAAGATGG | 27342 |
| rs568577429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732750 | CTTGCTGTCTCTCTC[A/G]CTCTCTTGCTGTCTC | 27342 |
| rs568598017 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66682042 | GCTCGCACTTCCTCC[A/C]GTCATCAGCCAAAGG | 27342 |
| rs568622418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738542 | CGAGACCAGCCAGGG[C/T]GACATGGCAAAACCT | 27342 |
| rs568666956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732374 | TGGCTCCCCTGCTGC[C/T]CACCACCCACCAAGA | 27342 |
| rs568684389 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681581 | TTTGTAAAATTTCTT[C/T]TGTAGAGATGGGGGC | 27342 |
| rs568685455 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738019 | TGTGTTTTTTGTTTT[G/T]TTTGTTTTTTTTTTT | 27342 |
| rs568688856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743113 | AGGAGTTTGAGACCA[A/G]CCTGAGCAACATGGT | 27342 |
| rs568690417 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766016 | CTTTTGCCCATTTCT[C/T]TTGGAAGGGAAGAAA | 27342 |
| rs568691789 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781282 | CTTTATAGAAAAAAG[-/A]AAAAAAAATTAAAAC | 27342 |
| rs568701166 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744912 | AAAAAAATGTTATCA[G/T]CCGCACACGGTGGCT | 27342 |
| rs568716461 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712433 | TGCAACCTTTACAAA[C/G]TTATTTATAGTTTTA | 27342 |
| rs568719918 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798147 | CAGTAGATGTCCTCT[C/T]TCCTCATTCCTCCCA | 27342 |
| rs568729702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800427 | TTCTCTTTATCTTCC[C/T]GTGTCAACTCCTGTT | 27342 |
| rs568745027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754012 | ACTAGGCCATTTTTT[C/T]TTTTTTTTGAGACAG | 27342 |
| rs568799204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737493 | TTTAGATCCGGATTT[C/T]GGGGCTCAGCCTTGC | 27342 |
| rs568816170 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711950 | TTGACCTGTGTCTCA[C/T]TGCCAATACTACACT | 27342 |
| rs568855954 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747226 | GAATAAGTATGTGTT[C/T]ATGAATGCGTAAAAT | 27342 |
| rs568862156 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774655 | GTCCCAATAACTTGG[A/G]AGGCTGAGGGATGAG | 27342 |
| rs568872544 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746106 | ACTATTGTTACAATA[C/T]GTAAACATGTGAAAT | 27342 |
| rs568925059 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770929 | TTTGGAGAATTGTTT[A/T]TTGAAGTCCTTTTCC | 27342 |
| rs568936987 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725413 | CATCTACTTTTTGTC[A/T]TTATAGATTTGTCTA | 27342 |
| rs568969872 | in-del | -/AA | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707675 | ACTGGGCAAAAGAGC[-/AA]GACTCCATCTCAACA | 27342 |
| rs568970286 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718262 | AGGTGGGAGGATTGC[-/T]TGAACCTGGGAGGCA | 27342 |
| rs568982808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806717 | GGTGTGATCTCAGCT[C/T]ACTGCAACCTCCGTC | 27342 |
| rs569000433 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694747 | CAATGGGACAGAGGG[G/T]GGAGGGGAGGGGGAG | 27342 |
| rs569022279 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66685248 | AACCTCCACCTCCTG[A/G]GTTCAAGTGATTCGC | 27342 |
| rs569085480 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776509 | ACCAGTCTGGGCAAC[A/G]TGGTGAAACCCCGCC | 27342 |
| rs569121446 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693366 | CTGTTGCACAAACTC[C/T]GTCTCTCCCCTGGCT | 27342 |
| rs569132099 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682889 | AGAGCCGGGGGATGC[C/G]CATCACGGCAGTTTA | 27342 |
| rs569154868 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725869 | CTAATCTGAGGGGGA[C/T]GTGGACCCTTCCATG | 27342 |
| rs569159442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699062 | GCCGCATGGAGGAGC[A/G]GGGAGATATCTGGCT | 27342 |
| rs569160702 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688619 | CCAGCAAAACTCGAA[A/G]ACTCACAAATATATG | 27342 |
| rs569183654 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732282 | CGTCTGGACACGGAG[C/T]CTCATTGAGCAGGGG | 27342 |
| rs569185549 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770969 | ATCGGATTATTTGGG[G/T]TTGTTGTTGTTGTTG | 27342 |
| rs569194940 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808347 | CAGTCTCCCAGGTAG[C/T]GGGGATTACAGGCGC | 27342 |
| rs569204697 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787388 | TTGCTCTGTTGCCCA[C/G]GCTGTAGTGCAGTGG | 27342 |
| rs569217010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793744 | TGATCACAAAGTGCC[A/G]TGAGTGCTTGGCCAT | 27342 |
| rs569217284 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786693 | ATAGGTGTGAGCCAC[C/T]GCGCCCAGTGCTATT | 27342 |
| rs569223009 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803027 | TAAAAAATCTTACCC[A/C]ATCTTACCCAATTCT | 27342 |
| rs569225216 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748939 | CCAAAAACTGTTTTA[C/T]GTCATAAGAGCAAGG | 27342 |
| rs569245247 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682524 | GGCCGTGCCCCGACG[G/T]CCTGACCTGGATCAC | 27342 |
| rs569254384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760959 | TTGTATTTATTAAGC[A/G]TTTAGTACGTATCAT | 27342 |
| rs569269296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781084 | CATCTTGCTGTTTGT[A/G]TTTATCCCAACTTGT | 27342 |
| rs569305087 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781180 | TGTTAGCTATACCTC[-/T]TTGTTCTGTTTTGTT | 27342 |
| rs569323755 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66738817 | TTCTGTAATCACAAA[A/C]GTCAGTTAAGAGCTT | 27342 |
| rs569324083 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744048 | TTTCTTTTCTTTTTT[C/T]TTTTTTTAAGACGGA | 27342 |
| rs569324880 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688037 | TTGCAGTGAGCTGAG[A/G]TCGTGTTATTGCACT | 27342 |
| rs569329537 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767093 | CTGCAACCTCCATCT[C/T]CCCGGTTCATGCGAT | 27342 |
| rs569345314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737601 | AAGACTGATATAGTG[C/T]TGTTCTCCTTTAATT | 27342 |
| rs569399780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706441 | TTTTAGACGGAGTCT[C/T]GCTCCGTCCCCAGGC | 27342 |
| rs569432866 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737452 | CTGGGTAGGGGGGGG[C/G]AGTCTAAAACAATAT | 27342 |
| rs569485787 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742611 | AAGGAGGTGCCTATT[A/T]ATTTATTTATTGAGA | 27342 |
| rs569492745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712405 | GCTAGCACATAAATA[C/T]ACAATTCTATGTTGC | 27342 |
| rs569572291 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705997 | AAGCTCCGCTTCCCG[G/T]GTTCACGCCATTCTC | 27342 |
| rs569636632 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759117 | ATAGTCAAGATACAG[-/A]ACTATTCCATTACCC | 27342 |
| rs569686588 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695600 | TGGAGAGAGTGGGTC[A/G]TGAGAAAGTGAGGGA | 27342 |
| rs569686744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701732 | CAGGCTGGTCTTGAA[C/T]TCACGACCTCAGGGA | 27342 |
| rs569722667 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782446 | TTTACATAAAACATA[G/T]CACAGTGTACATACC | 27342 |
| rs569722989 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701137 | TAGGAAGAAGGACTG[C/G]AGGGGTAGACAGGCA | 27342 |
| rs569739604 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749341 | AGTAAACAGTGGGTG[A/C]AACTGCCCTTGCCTA | 27342 |
| rs569744197 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690055 | GACAAAGGCACTACA[A/G]GAAAACAACTGATCA | 27342 |
| rs569765822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789256 | TAGGCTTTAATTATT[A/G]TGAGAACTTCAGCAG | 27342 |
| rs569776410 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788736 | GTAATCCTAGCACTT[C/T]GGGAAGCCAATGCGG | 27342 |
| rs569789395 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688775 | AGTGCTCAGAGGGAA[A/G]TGTATAGCTGTAAGC | 27342 |
| rs569805005 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707752 | TTTATCTTCCCTCCA[A/G]TTACTGCAGTTTTTA | 27342 |
| rs569835140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748607 | ACAAAGAATAAAATC[A/G]TAACGGCTAGTTCAA | 27342 |
| rs569838059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801853 | GTTCTTAGCCAGGCA[C/T]CAGTGGTCCCCCGGA | 27342 |
| rs569839745 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795289 | CTGTGAGACGGACAA[G/T]GATCCCGTCTTTAGC | 27342 |
| rs569860026 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717265 | TTTCTGCTTAGAATT[A/G]ATATTTTACCACTTG | 27342 |
| rs569895542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763267 | GAATTAAGCATCGGC[C/T]AGCCTGGGTTTTTAT | 27342 |
| rs569896288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713223 | CTCAGCTCACCGCAA[A/G]CTCTGCTTCCCGGGT | 27342 |
| rs569900333 | snp | A/G | 6.59544e-05 | 0.0057422 | missense | RABGEF1 | GRCh38.p7 | 7:66809027 | GATGCTTGCTTAGGC[A/G]TCAAGCAAATGTATA | 27342 |
| rs569937081 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690746 | AAAAATTAAATTTAC[A/G]AAAAGAGAAAACACT | 27342 |
| rs569950063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794710 | TTATTCATATTAAGC[A/G]GTTAATGCCACTTTT | 27342 |
| rs569951347 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750945 | TCTTAATTTTAGAAA[A/T]ACTTTTCAGATCTAG | 27342 |
| rs569970188 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769254 | CAAAAATAGTGCACA[G/T]TGCATACTGTCCAGA | 27342 |
| rs569983522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801096 | GAGGTCGAACACTCT[C/T]TAGGACTTCTGAAAG | 27342 |
| rs570007840 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797118 | CAGCCTGGGCAACAT[C/G]GTAAAACCCCATCTC | 27342 |
| rs570016066 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757120 | AACTTACACATTTTG[A/G]AATGTTTGACACTGT | 27342 |
| rs570023305 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751445 | TTCCTGTTGGTTTTT[A/C]GTTATCTGAATGTGA | 27342 |
| rs570143538 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781259 | TACCTTCAAGTAGTA[G/T]TATATCACTTTATAG | 27342 |
| rs570145916 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708889 | TTGTTATTTATCATG[A/G]AATTTGTGATGGGAG | 27342 |
| rs570164838 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684138 | GTTTTTAGCTGGGTC[C/G]TTATGTGGTTAAAAT | 27342 |
| rs570166023 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721333 | TGCCATATAGTGACT[G/T]AATACAAATTTATTG | 27342 |
| rs570166031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714614 | TGCTTACCTTGGGTT[A/G]ATTTTACTCTTTTTA | 27342 |
| rs570182124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748517 | TCGTGGGGGTATCAC[A/G]ATGGAACAGTCTGAC | 27342 |
| rs570192996 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802666 | AAAGAGTTCCACGAA[A/G]AATTCCTTCAGGCCA | 27342 |
| rs570205207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684783 | GGGACTGCAGGCACC[C/T]GCCACCATGCCTGGC | 27342 |
| rs570207304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756322 | ACCAGATTCCCTCAT[A/G]CACTGTAGGTGGGAA | 27342 |
| rs570221432 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810633 | TCAGTGGAACCTTCT[A/G]TAACCTAAATATACC | 27342 |
| rs570265406 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733593 | ATCCCAGCTACTCGG[C/G]AGGCTGAGGCAGAAG | 27342 |
| rs570273011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770130 | TATGAGCTTCATGAG[A/G]GTAAGGACATGTTCT | 27342 |
| rs570294812 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754872 | TAAAACTATGATATG[C/G]CTTTGAGAAAAAAGT | 27342 |
| rs570320380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788703 | CTGATACTGAGCTGG[A/G]CACAGTGGCTCACGC | 27342 |
| rs570356626 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689671 | AGTTGGGCATGGTGG[C/T]AGGCACCTGCAATCC | 27342 |
| rs570363279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754202 | AGAGACGGGGTTTCA[C/T]TATGTTAGCCAGGAC | 27342 |
| rs570384082 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726077 | GGGCACAAGGCCACA[A/T]CTGTCTGCAGGAAGC | 27342 |
| rs570390340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695985 | AAAAAAATAAAGTGT[A/G]GATGACTCTTTGAAG | 27342 |
| rs570424167 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738138 | TGATCCTATCACCTC[C/G]GCCTCCAGAGTAGCT | 27342 |
| rs570435799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743175 | TAGCTTGGTGTGATG[A/G]CGCCTGCCGTAATGC | 27342 |
| rs570485444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700343 | TTGAAGGGGTCCTGC[C/T]TGTGTAGGGTTGCGT | 27342 |
| rs570500158 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713207 | AGTGCAGTGGTGCGA[C/T]CTCAGCTCACCGCAA | 27342 |
| rs570522214 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706957 | TGGCTAATTTTTTTT[G/T]GGTATTTTTAGTAGA | 27342 |
| rs570569191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725247 | TTAACATGTACACTT[C/T]AATGACCTTTAGTAT | 27342 |
| rs570570715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808159 | CCACGGTCACTCACT[A/G]TTGTTGTTAAGTGAA | 27342 |
| rs570578378 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688605 | CTAGACATCAGTAAC[C/T]AGCAAAACTCGAAAA | 27342 |
| rs570588758 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683997 | TCTCCCGCCTCAAGT[G/T]TCCCAATGTGCTGAA | 27342 |
| rs570594192 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745579 | TGAGACCAGCCTGGA[C/T]CAAGATGGCAAAACT | 27342 |
| rs570596731 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802553 | AGGGAAATTATTAGA[C/G]AGCAGTGAGTTTCCT | 27342 |
| rs570615680 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801024 | GACAAGTAACAAATA[C/T]GAGGTCTGTTGAAGA | 27342 |
| rs570616820 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767452 | AAAACTTTCTCGTGC[G/T]AATCCTTTATAGTCA | 27342 |
| rs570632702 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795183 | ACTCTGGCCTTGTGA[A/G]TGTCTCGGATTCCCC | 27342 |
| rs570674757 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683506 | GAGGAGAAGGGACAG[A/T]CAAGATACTTTCAGA | 27342 |
| rs570692145 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718703 | GAGTATGTACCACGC[A/G]GTGGCCAGCCTGGAA | 27342 |
| rs570700149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682790 | TTTGAAGCCTATGGT[C/T]CTGACTTCCACCCCG | 27342 |
| rs570724571 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710944 | GGCCAGGAGTTTGAG[A/G]CCAGCCTGGGCAACA | 27342 |
| rs570725958 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748326 | TTTTAGATTATCTAG[A/T]TGAGTAGGTGGATTG | 27342 |
| rs570742955 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800607 | TTGCTCGGGGAACCC[A/C]ATAAGAGGTTGAAGG | 27342 |
| rs570744711 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775652 | TTTGCTTATGAAATT[A/C]ATCCCCATCCAAATG | 27342 |
| rs570744744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768247 | TGTCGTCTTTCTCTT[A/G]TAAGGATGTTCAATA | 27342 |
| rs570750343 | snp | A/G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763432 | TCAAATTTCTTGGCT[A/G/T]TTAGTCTCCTCCAGC | 27342 |
| rs570761539 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708352 | GAGTGCAGTGGCGCA[A/C]TCTTGGCTCACTGCA | 27342 |
| rs570771206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807298 | AAAGTAAAAAGTTTC[C/T]AGCTGACGAACCCCA | 27342 |
| rs570805110 | snp | A/G | 0.000123419 | 0.00785456 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775197 | CCTTGGAGAATATCT[A/G]GGTCATTCTAATCCT | 27342 |
| rs570815088 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762618 | AAAAAAGAAAAAAAA[G/T]AAATAGGACATGAAG | 27342 |
| rs570823240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720850 | TTAGCAGAACCAAGT[A/G]TCAATTGAATTTCCA | 27342 |
| rs570902474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728609 | CCACCTCTATCCCCA[A/G]CTTCATTTTCACCTC | 27342 |
| rs570913277 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709651 | ATTAGCCAGGCATCT[C/T]GTAATCCCACCTACT | 27342 |
| rs570928005 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720340 | GTAGCTAGGACTACA[A/G]GCATGCACCACCACG | 27342 |
| rs570997689 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690164 | TGGAGTGCAGTGGTG[A/C]GATCTTGGCTCACTG | 27342 |
| rs571008716 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697123 | GGTGGTGAGGGTGGA[A/G]GGGGTGCAGAGCAGG | 27342 |
| rs571051228 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722301 | AAAAATTAGCCAGGC[A/G]TGGTGGTGCGCGCCT | 27342 |
| rs571055910 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695553 | ATCCATCTGGGGAGG[A/C]CTGGGGACAAAAGCC | 27342 |
| rs571064128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782295 | TTCTAGTTTGTCTCT[C/T]GCCCATCTAGTTCCT | 27342 |
| rs571091594 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738574 | GTCTCTACAAAAAAA[A/C]CCCAAAAACTAGCTG | 27342 |
| rs571118070 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811268 | TATCTCATATTGGTC[A/G]AATTCTTCTGGTATG | 27342 |
| rs571153370 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765494 | AAAAACGACAAAAGT[A/C]GTTAGGGGACCAGGG | 27342 |
| rs571159019 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695040 | TGAGGCCCTGGGTGC[A/G]GCAGCTCATGCCTGT | 27342 |
| rs571167200 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692847 | CACAGAGTCCACACA[A/G]CTGCTGAGAAGTCAG | 27342 |
| rs571195982 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701101 | GGGGACTGTTTGTGA[G/T]CAGCCGTGTGGCAGG | 27342 |
| rs571202522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790112 | AGGAGGCAAATATGT[A/G]TAGCATTCAGGGCTT | 27342 |
| rs571216641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796351 | GAAATCTCCATTTGT[A/G]TACCTCAGAGAGCTC | 27342 |
| rs571230217 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776798 | TACGAAAAAGGGGGG[A/C]AAAATTAGTACCTGC | 27342 |
| rs571246938 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708275 | AGCCATGTAGTTTGG[G/T]TTTTTTTTTTTTCCT | 27342 |
| rs571250366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734822 | ACACTGCTGGTCGCT[A/G]TGGCTTCCTCCTGCT | 27342 |
| rs571264020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684963 | AGAGATGGAATCCCT[A/G]TATGTTTCCCAGGGT | 27342 |
| rs571295048 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771288 | GGACTACAGGCGCCC[A/G]CCACCACGCCTGGCT | 27342 |
| rs571317590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66740932 | TTGCGCGTCGGTGCC[C/T]CCCGCTGTCCTTCGT | 27342 |
| rs571324651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784412 | ATTTTGCCAATGTCA[A/G]CCAGAACTTGTGATT | 27342 |
| rs571326859 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751920 | CAAAATCTTAGGCTG[A/G]GCACATTGGCTCACA | 27342 |
| rs571352431 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740214 | CTGGACTCAAGCGAT[A/C]CTCCTGCCTGGGCCT | 27342 |
| rs571383240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776522 | ACATGGTGAAACCCC[A/G]CCTCTACAAAAAATA | 27342 |
| rs571383863 | snp | C/T | 0.000199197 | 0.00997791 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783860 | GGTTGAGAATAACCA[C/T]GTAGAAACATAGAGT | 27342 |
| rs571483096 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66755907 | TTTGTCCAAGCTAAC[A/G]TTTGGACAAATAATG | 27342 |
| rs571490256 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798798 | GTGAAACCCTGTCTC[A/G]TAAAAGTACAGAAAT | 27342 |
| rs571497644 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734788 | ATTGTTGTCATTTCT[C/T]GGTCTTCAAAAATGA | 27342 |
| rs571525159 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789467 | ATGGGCGGATCACAA[C/G]GTCAGGAGATCGAGA | 27342 |
| rs571574406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723125 | AGGCAAGCGCTGCCA[C/T]GCCCGGCTAGTTTTT | 27342 |
| rs571680406 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697718 | TTCTCCGGCCTCAGC[A/G]AGGTGGGGGGTGTTC | 27342 |
| rs571721527 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704239 | AAAGTTGCAACATTC[C/T]CCTAACCAAAATTTA | 27342 |
| rs571724676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709316 | GTTTTAAATTTTAAA[A/G]TGCATCTGTAATTGT | 27342 |
| rs571792962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716474 | GGTGTGGCGGCATGT[A/G]CCTGTAGTCCTAGCT | 27342 |
| rs571806116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758016 | GGGAAAAAAATCACC[C/T]GTAAGTTTTATTTCT | 27342 |
| rs571827399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732954 | CAGTCAGGGTGAGCT[C/T]GCAAAAGTGGCAAGT | 27342 |
| rs571838999 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798253 | AGTCTTCCAGGCTCA[C/G]TGGGGTGAGCCCCAG | 27342 |
| rs571855872 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758502 | ATGCAGTGCTCCAAC[A/G]GGAGCGATGTGTGGC | 27342 |
| rs571880568 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66685351 | ATTTTAATCTTCTCT[C/G]CTCTTTAGATGTTTG | 27342 |
| rs571891418 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803993 | TCTGCCAATCAGCAG[G/T]TGTGAATGTTGTGAT | 27342 |
| rs571914954 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738327 | CCCGGCCAGTCCTCT[C/G]TAGCTTAACCTTCAC | 27342 |
| rs571942480 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720461 | CCTCAGCCTCCTAAA[A/G]TGCTAGGATTACAGG | 27342 |
| rs571971789 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783229 | TTGCTTTTTTCTCAA[A/G]TAAAATGGGATTTGG | 27342 |
| rs571983012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762149 | CGAAAACCAATATAT[A/G]TTATAACACCACACT | 27342 |
| rs571990032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764163 | TTTTGGTTCTAGTCA[C/T]CCTACTGGATGTGAA | 27342 |
| rs572020643 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751316 | CATTACAGGCGTGAG[C/T]CACCGTACCTGGCCT | 27342 |
| rs572031454 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810228 | ATTTGACTTTGCAAA[C/T]GTCTAGACATGTTTT | 27342 |
| rs572044146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769424 | CAAAGATTGTTGTTT[C/T]AGACAAAGATTGAGA | 27342 |
| rs572046382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768400 | GGTTTGTTTTCTGAC[A/G]TCTGAGTTTTGAGAG | 27342 |
| rs572059500 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810111 | GGAGCAGGCACTGGG[C/T]CTGGAATGGAAGGCG | 27342 |
| rs572073813 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RABGEF1 | GRCh38.p7 | 7:66809426 | TATGGGGATTGTTTC[A/G]TTTTTCCTAGCAGGG | 27342 |
| rs572075452 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683759 | TTATTTATTTATTGA[C/G/T]AGAGAGGGTCTCACT | 27342 |
| rs572125386 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726731 | CTGCGAGGTCAGGTG[C/T]GGTGGCTCACGCCTG | 27342 |
| rs572139430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695664 | CTCACGCCTATAATC[C/T]CAGCACTTTGTAGAC | 27342 |
| rs572167762 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689726 | AGAATCACTTGAACC[C/T]GGGAGGCGGAGGTTG | 27342 |
| rs572168534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695243 | CTTGAACCTGGGAGG[C/T]GGAGGTTACAGTGAG | 27342 |
| rs572187354 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784009 | TAAAACCCAACTCTT[A/T]GGCTAGTACTTTTCC | 27342 |
| rs572207698 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700799 | AAGACAGAATGGCCC[A/G]AGGCCTGGACACTCT | 27342 |
| rs572211160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743648 | CTGGGACTACAGATG[C/T]CCGCCACCATGCCTG | 27342 |
| rs572217582 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743257 | GGAGGTTGTGGTGAG[C/T]CAAGATTGTACCAAT | 27342 |
| rs572225559 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701218 | AGAAGTAACAGGGAG[C/G]CTGGGCACAGTAGCT | 27342 |
| rs572241982 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774912 | GATGTAGCAGCTGTC[C/G]CATTCTGTAGCAGTT | 27342 |
| rs572251452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783376 | TTTCAGTGTTCATGA[C/T]TGAATATATAGATCA | 27342 |
| rs572257795 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737973 | CTCATGAGGCCGCTC[C/T]GGTCTATTTTAAAGC | 27342 |
| rs572290181 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751080 | TTGTCGCCTAGGCGG[G/T]AGTGCAGTGGTGTGA | 27342 |
| rs572291372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788273 | AATATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 27342 |
| rs572343664 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735368 | AAGACTTTATAGCAT[A/T]GTAGTTTAGATTATG | 27342 |
| rs572350959 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750265 | TCTATGAGAAATTCA[A/T]TGGCAAAGTGTTTTC | 27342 |
| rs572353824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699900 | GCAAACCCAGGGCCA[C/T]TGGAGAATGACATGG | 27342 |
| rs572359548 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749732 | ATCTCAGCACTTTGG[G/T]AGGCCAAGGCGGGCG | 27342 |
| rs572361404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756464 | GTCTGCTCAAGGTCA[C/T]GGTCTGCTCATAACC | 27342 |
| rs572390187 | snp | C/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755028 | GGCCAGGCACGGTGG[C/T]TCACACCTGTAATCC | 27342 |
| rs572409271 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696355 | AGGTGTGAGTCATCC[A/C]GTGTGGCCAAGGGAC | 27342 |
| rs572410075 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740349 | AAGCGTCCCTCGGCG[A/C]AGTAGCTCCGCTCCA | 27342 |
| rs572456930 | in-del | -/GG | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806833 | ATTTTTAGTAAAGAC[-/GG]GGTTTCACCTTGTTG | 27342 |
| rs572465595 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702832 | TGGGTTGTTTGTCTT[A/T]TTGTTGTTCAGTTTT | 27342 |
| rs572488669 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710144 | GAAATCATTTACTAT[A/T]TACTCTTTTTGGCAT | 27342 |
| rs572532840 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802741 | AGATCCCTGGGGGTG[-/T]TTGTCTTTCTTTATT | 27342 |
| rs572542866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790284 | TGTTCAGCAAGCACT[A/G]CCAAGCTGAACCCTG | 27342 |
| rs572703427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66685515 | AGAAAAGATTCTTGA[A/G]GTGAATGTATACTCA | 27342 |
| rs572708588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721004 | CTCACTGCAACCTCC[A/G]CTTCCCAGGTTCAAG | 27342 |
| rs572721828 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803686 | ACGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 27342 |
| rs572723121 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762742 | CCCCAAAAGAATAAT[A/C]ATAAATAGGACATGG | 27342 |
| rs572729291 | snp | C/G | 0.000296516 | 0.0121725 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795492 | AGCTACAAGCAGCCT[C/G]TTTGTCTCTCTGTTT | 27342 |
| rs572753950 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791750 | CAAAGATAGACATCC[A/T]CTTGTCAATGTCTTA | 27342 |
| rs572763986 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807867 | CCGACTGTTTCCCAG[C/G]CTGGTCTGAACTCCT | 27342 |
| rs572780137 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745959 | AGTGATACCCTGTCT[C/G]TATAAAAAGAAGTTT | 27342 |
| rs572785010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714070 | TGATGTAAAGGTAAT[A/G]TTGGCTTTATACAAC | 27342 |
| rs572791604 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66685138 | AATGTTTTCAGTATA[C/G]TGCTGGATTATTTGC | 27342 |
| rs572799546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692374 | TGTAAAAGTTCTGCA[C/T]CTACAGCATTGTCTT | 27342 |
| rs572809957 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777669 | TGGCTTCTACCTACC[C/T]ATAATCCCAGCTACT | 27342 |
| rs572821358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716669 | TTTTTTTAAAAAAAA[C/T]TCTTCTGTCATTGTC | 27342 |
| rs572855385 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711594 | TACTCTATTCTTTTC[-/T]TTTTTTTTTTGAGAT | 27342 |
| rs572856008 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788350 | CTCGGGAGGCTGAGG[A/G]AGAAGAATCACTTGA | 27342 |
| rs572864676 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769382 | TTCTAGCTGTCACCC[A/G]TGTGTCTGCACACCT | 27342 |
| rs572876791 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766703 | CTTTCCATTCCCACT[A/G]TTACCTCTTATTTAT | 27342 |
| rs572931787 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751955 | TAATCCCAGCACTTT[C/G]GGAAGCCAAGGTGGG | 27342 |
| rs572959817 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680606 | GGCACCTAGGAAGAA[C/T]TTGAGAAACGAATCA | 27342 |
| rs572989457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722642 | TCTAAGAGTTTTGTC[A/G]CCTTAGCTTTTATAT | 27342 |
| rs572998782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758165 | GAATAGGAAGCGGAC[C/T]GCCAAGAAGGATAGA | 27342 |
| rs573030226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764275 | TGCATATCTTTCTGG[A/G]GAAATGTCCATTCAG | 27342 |
| rs573052458 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779999 | AGTAACTTGTATGAT[C/T]ATAACTAGCTAGTAG | 27342 |
| rs573056108 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729772 | TGACCCTAGATGATG[A/G]ATGGATGTGGCCAGG | 27342 |
| rs573063345 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770818 | AGTAGCCATCCTAAT[G/T]GGTGTAAAGTGATAT | 27342 |
| rs573089960 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810919 | CATCTGTGTCATCAC[A/G]CACTGAAGACAGGAA | 27342 |
| rs573097100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736400 | CAACCTATACCACTA[C/T]ATGGGGCCATTTAAC | 27342 |
| rs573109592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735965 | GATGGCTGATAATAA[A/G]GCTGATAAAACATCA | 27342 |
| rs573220002 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724151 | GGTTAACAGCTTTTT[C/T]CCCCCAGCACTCTAA | 27342 |
| rs573221930 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759562 | AAAGGAGGTTTAATT[A/G]GCTCACAGTTCTACA | 27342 |
| rs573228111 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743176 | AGCTTGGTGTGATGG[C/T]GCCTGCCGTAATGCT | 27342 |
| rs573234470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799288 | TGGCCACAGTTTATC[C/T]TTGGAGCTCTTGTTT | 27342 |
| rs573247639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704577 | GCACTTTGGGAGGCC[A/G]AGGCGGGTGGATCAC | 27342 |
| rs573270868 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750459 | TTTTTGGTTTATGAC[A/G]TATTAGGGAACAAAT | 27342 |
| rs573275766 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681793 | CGCAGTGGCTCCGCT[C/G]CACCTCCCATTCGCG | 27342 |
| rs573281342 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765743 | CCCATTTCCAAAACT[C/T]GAAGCAAAAGACTCT | 27342 |
| rs573292200 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693530 | GACTACTCCTCCTCC[C/T]CTCCCTCGGCTGCCA | 27342 |
| rs573365568 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741616 | GAAATTTTCCCAGGA[C/G]GAGTTTACCGGAGCA | 27342 |
| rs573379643 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698289 | GCCCCTTAGACCATG[G/T]TTCCCAGCCAGAGCT | 27342 |
| rs573384707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772868 | AGTGAGCTGAGATCA[C/T]GCCACTGCACTCCAG | 27342 |
| rs573401093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686229 | GAGGTTGCAATGAGC[C/T]GAGATTGTGCCACTG | 27342 |
| rs573407989 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693060 | GAGCCGGCTGGTCCC[A/C/G]TGGCCTTCACTCAGC | 27342 |
| rs573413210 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721660 | ATAATCCAGGATAAT[A/T]TCTCCACCTCAAGAT | 27342 |
| rs573438940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785883 | CATCTGGGGGGGAAA[A/G]AAAAAAAGTCTTTGT | 27342 |
| rs573444902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697804 | GGTCACGTCTGGGAC[C/T]CAGCAGAACTGCGGT | 27342 |
| rs573454953 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66740991 | TTCCCCGTTCCAGGC[C/G]GCCCTCGGCTCCCTT | 27342 |
| rs573494058 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810902 | ATCTATTAAGCTTGA[C/T]ACATCTGTGTCATCA | 27342 |
| rs573502869 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698912 | GGGGTTCCATGGTGT[A/G]CTCTTTCCCCTTGGC | 27342 |
| rs573555124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691014 | GAGAATCGCCGGAAC[C/T]GGGGAGGCAGGGGTT | 27342 |
| rs573567974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796715 | TCCTGTCTCAGCCCC[C/T]GAGTGGCTGGGATTA | 27342 |
| rs573585704 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762865 | GATGTGAAAGCTTAG[A/C]CCTAAACGATGAGAA | 27342 |
| rs573592255 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697176 | CTCCGTCCAGAAGGC[A/G]AGAGGAGGCCTGGGC | 27342 |
| rs573596098 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751206 | TGGCTAATTTTTGTA[G/T]TTTTAGTAGAGACGG | 27342 |
| rs573631829 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790384 | GTGCCAGTGTTGTAA[C/G]AAGGTTTGAGGGAGG | 27342 |
| rs573667514 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759750 | ACAGAACCACAGGGG[-/A]TGGTGCGAAACCATT | 27342 |
| rs573681060 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803532 | TTCGCTGTCCCCCAG[A/G]CTTGTTGGAAAAGGG | 27342 |
| rs573681096 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754064 | CTGGAGTGCTGTGGC[A/G/T]CAATCTTGGCTTACT | 27342 |
| rs573728995 | in-del | -/AGAG | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763294 | TTATTTGGAGGTGAT[-/AGAG]AGAGTCTCCTTCCAG | 27342 |
| rs573732830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765098 | GGTGTAGCACCAGAG[A/G]GTGAAGGTCATGGGT | 27342 |
| rs573733784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757564 | GAATGCAGAGGGAAC[A/G]CTATAGGAATATGTA | 27342 |
| rs573772880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684493 | AAGGTCTCTATCTGT[C/T]GTCCAGGTTGGAATG | 27342 |
| rs573790875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727866 | TGGTGGGATTCCCAG[C/T]GGCTGCCTTGGAACA | 27342 |
| rs573804995 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770658 | CCAGCTAGTTGTTGT[A/G]TTTTTTGTAGAGATG | 27342 |
| rs573815215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734499 | TGGGGTTTTGCTATG[C/T]TGGCCAGGCTGGTCT | 27342 |
| rs573824474 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735838 | CTCTTTCCTTTATAA[A/G]TCACCCAGTCTCAGG | 27342 |
| rs573843577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769597 | GCCTGGACGTAGATG[C/T]ATTGCAGAAAGTGGA | 27342 |
| rs573868647 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776755 | AAGTTGTTTCTTGGT[G/T]GGCTGCCAGTTGTAG | 27342 |
| rs573883636 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777121 | TTATTCTTCTGATAG[A/C]ATTATCTTGCAGGGA | 27342 |
| rs573896131 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774960 | TCTGTTCCAGCCTTG[A/C]GCTTGTTAGGGAAAA | 27342 |
| rs573899814 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740637 | AAGGCCCCGGAAGTG[A/G]CGTTTACGCGCCGCG | 27342 |
| rs573909018 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691665 | TATCCAATAAATTAC[A/C]TGAGAAATTCAACAT | 27342 |
| rs573946159 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681326 | AGTAAACAGTATCCA[A/G]TTTGTGACTCAACCA | 27342 |
| rs573961218 | in-del | -/AAAT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772917 | CTCTGTCTCAAAAAA[-/AAAT]AAATAAATAAATAAA | 27342 |
| rs573994177 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689460 | AATGAAATGGCAAAT[C/T]TCTAGAAACACAAAA | 27342 |
| rs574013229 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729704 | TCTCCAGGTGGGTCT[C/T]CTGCCATCACTAAAT | 27342 |
| rs574067629 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780031 | GTTAATCCTCATTTA[A/C]ATTTTAAAAGGGTTT | 27342 |
| rs574070310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729267 | GACCTCCACCATTAC[C/T]ACCATCCTCGCCTTC | 27342 |
| rs574126162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777847 | TTGTTTTAAAAATAT[A/G]TATGCAGAATGATTT | 27342 |
| rs574172774 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786751 | CTGAAGCTTGTTTAT[G/T]TTGCTCTTTTTTCTT | 27342 |
| rs574181001 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779520 | TAAAAAAAGAAAAAA[A/T]AATTAAAAAATTAGC | 27342 |
| rs574205387 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694314 | TCTTTTGACTTGGCA[A/G]GGTGGTTTGTGGAAT | 27342 |
| rs574233375 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703501 | GTAAAGGTCTAACTT[G/T]ATTTTTTGGCATGTG | 27342 |
| rs574295544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764422 | GTGGGTTCTGTTTTC[A/G]TTTGATAAGGTCCTC | 27342 |
| rs574298272 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703013 | TCTCGCTCTGTCGCC[A/G]CCCAGGCTGGAGGGC | 27342 |
| rs574321005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709424 | ACATAAGCATCACTA[C/T]AACTAGTGCTATCTA | 27342 |
| rs574342684 | in-del | -/A | 0.438246 | 0.16451 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718565 | AGAAGTTTAATTTAT[-/A]AAAAAAAAAATAGGC | 27342 |
| rs574364286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784957 | AGAACTAAAAACTGA[A/G]GTTTTGTATTTATTT | 27342 |
| rs574367680 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699122 | GTGGGGAGGCGAATT[A/C]CAGGCCCCTCTGGGT | 27342 |
| rs574406945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706048 | GCTGGGACTACAGGC[A/G]CCCGCCACCGCGCCC | 27342 |
| rs574415105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747268 | AGAGAGTATTAAGCT[C/T]TTTAATTTTCCCCCA | 27342 |
| rs574446949 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786021 | ACCTGTTTAAAAACT[A/G]CCCAGTCAGCCTTGC | 27342 |
| rs574474251 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713246 | TCCCGGGTTCATGCC[A/G]TTCTTCTGCCTCAGC | 27342 |
| rs574477117 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737051 | TATATATATGAGGGG[A/G]GAGAGAGAGAGAGAG | 27342 |
| rs574488214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793242 | TTGGAATATTTACAC[A/G]TATATAAGATAACTT | 27342 |
| rs574491042 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736627 | CAGGTGATGAGGGTG[A/T]GGCAGGTGGATCACT | 27342 |
| rs574510975 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801203 | GAGAGTGTCAGGGCC[C/T]GTGGCTGATGGTGGA | 27342 |
| rs574554843 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746864 | ATAGTGCGATCTTGG[C/G]TTACTACAACCTCTG | 27342 |
| rs574562590 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712742 | CCTCCCAAAGTGCTG[A/G]GATTATAGGCGTGAG | 27342 |
| rs574589063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799209 | GGTGATGTGTGTGGG[C/T]CTGGGATTGAGTGGT | 27342 |
| rs574616348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752895 | GGGACAAAAGTGAGA[A/G]AACACTGTCTCTGCA | 27342 |
| rs574621719 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800662 | ATGGACCTGGGACTT[G/T]TGTTTTTCCTGACTC | 27342 |
| rs574642815 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787134 | CAGGTTCCAGTGATC[A/G]TCCTCCCTCAGCCTC | 27342 |
| rs574657507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765638 | GGGGTATGTCTATTT[C/T]ATTCTGTAGACTGTC | 27342 |
| rs574664135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732724 | CGCTCACTCTCTCTC[A/G]CTCTCTCTCTCTTGC | 27342 |
| rs574686546 | in-del | -/ATT | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787025 | TACAACATAACTTGA[-/ATT]ATTATTATTTCTTTT | 27342 |
| rs574692872 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693437 | GCCTGGCTCAGGGTG[A/G]GAAGGTAGGTCTCAT | 27342 |
| rs574699305 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688169 | TTTAAGCCAACAATG[A/G]TTATGAGAGACAAGG | 27342 |
| rs574706747 | in-del | -/AAAAC | 0.00398564 | 0.0444627 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714937 | AGACTCCGTCTCAAA[-/AAAAC]AAAACAAAACAAAAC | 27342 |
| rs574710017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694648 | ATGTCACGATACCCC[A/G]GCCAAATAGTGTGAG | 27342 |
| rs574728974 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787621 | ATGTGCCGGGATTAC[A/C]GGATTGAGCCACAAT | 27342 |
| rs574758015 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717370 | GCATCTATAAACATT[C/G]AAATTCCATTAGAAT | 27342 |
| rs574759899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710339 | ACCAGTAAAGATGCT[A/G]TAGGCATCCAGATAA | 27342 |
| rs574763511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706679 | TCGGCCTCCCAAAGT[A/G]CTAGGATTACAGGTG | 27342 |
| rs574785246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694514 | CAGTGGGAAGCCAGC[A/G]AAGGGCATTGAGCTA | 27342 |
| rs574786368 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751221 | TTTTTAGTAGAGACG[A/G]GGTTTCACCGTGTTA | 27342 |
| rs574846208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719521 | TTTTATGTAAATCTT[C/T]CTGATAAAAATTTCA | 27342 |
| rs574866307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785958 | TACCACCAACTAAAC[C/T]TTCTAGATGGTATCC | 27342 |
| rs574872472 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697878 | AAAAAGGTCCAGGAG[A/T]CCGAGAGCAAGTGAG | 27342 |
| rs574875545 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758929 | GACTTCAAATCCATA[A/G]GAAGCTGTAAATACA | 27342 |
| rs574889591 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781954 | CTGCTGTTTGTCTGT[C/G]ATCCAGTGTCTGAAA | 27342 |
| rs574931081 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725521 | CATGTATCAGTTCTT[A/G]TTTCTTTTTATTGCC | 27342 |
| rs574932793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755037 | CGGTGGCTCACACCT[A/G]TAATCCCAGCACTTT | 27342 |
| rs574945083 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754526 | CAGTGGGCAGATCAC[A/G]TGAGCCCAGGAGTTG | 27342 |
| rs574951486 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704811 | TGAGACTCCGTCTCA[-/A]AAAAAAAAAAAAAAA | 27342 |
| rs574966672 | in-del | -/TTAT/TTATTTAT | 0.0260635 | 0.111142 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683731 | CAAGGAGGTGCTTAT[-/TTAT/TTATTTAT]TTATTTATTTATTTA | 27342 |
| rs574976601 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718149 | GGAGTTCGAGACCAG[C/T]CTGGCCAACATGGTG | 27342 |
| rs574982638 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66682147 | GGTGTGTGTGAGGCT[A/G]GAGCGGACTGGGGAA | 27342 |
| rs575009836 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760616 | GCCCGGCTAATTTTT[G/T]TATTTTTAATAGAGA | 27342 |
| rs575042171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791928 | ACCAGCCTGGCCAAG[A/G]TGGTGAAACCCTGTC | 27342 |
| rs575053526 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738331 | CCAGTCCTCTCTAGC[-/T]TTAACCTTCACAAAG | 27342 |
| rs575058175 | snp | A/T | 0 | 0 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798468 | CTGGGCAGGCTGAAG[A/T]TGTGGAGCCCAAGGT | 27342 |
| rs575074393 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766418 | ATCTCTTACTATAGG[A/T]TGTAGTAGATGGTCT | 27342 |
| rs575086761 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773573 | AAGACTAGAGAATTT[C/G/T]CATTTCTGACAAGTT | 27342 |
| rs575091426 | in-del | -/AAACA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684443 | GCAAGACTTCGTCTC[-/AAACA]AAACAAAACAAAACA | 27342 |
| rs575109021 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681215 | TTTCTTTCTTTCTGT[A/G]ACTGCACCTTTCACC | 27342 |
| rs575119193 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731924 | CCCCTGAGATGTGCA[C/G]AGAAGCCCCCTGTCT | 27342 |
| rs575131378 | snp | A/G | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754730 | ATCTAACAAATCTGA[A/G]TAAATACATTTCACG | 27342 |
| rs575149412 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765008 | GATATCTAGCATAGT[A/C]TCCTTATTTTAATGA | 27342 |
| rs575185526 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764449 | CCTCTGAAGCACAAA[C/G]ATTAAAATTTTGTTG | 27342 |
| rs575213544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711045 | TGTACCTGTAGTCCC[A/G]GCTACTCAGGAGGCT | 27342 |
| rs575215718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752780 | GTCTTCCAAGTGATA[C/T]TGATGTACATTCAAG | 27342 |
| rs575223946 | in-del | -/T | 0.124491 | 0.216211 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713145 | TTTTCTTTTCTTTTC[-/T]TTTTTTTTTTTTTTG | 27342 |
| rs575233249 | in-del | -/AA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687485 | CTGTTGTTTAAGCCA[-/AA]AAAAAAAAAAAAAGA | 27342 |
| rs575270215 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749960 | GCGTGGGCGACAGAG[C/T]GAGACTCCATCTCAA | 27342 |
| rs575287598 | snp | A/G | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754867 | AAAGCTAAAACTATG[A/G]TATGCCTTTGAGAAA | 27342 |
| rs575301495 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741709 | GTTTTTATTTATTAT[A/T]TTTTTCGACATGGGA | 27342 |
| rs575313500 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746784 | TCCTGCCACCACGTC[C/T]GGCTAATTTTTTTTT | 27342 |
| rs575320116 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697880 | AAAGGTCCAGGAGTC[C/T]GAGAGCAAGTGAGGC | 27342 |
| rs575348459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724726 | TCATGGTTTTCATCA[A/G]ATTTATAGTTTGAAA | 27342 |
| rs575380488 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717653 | AGCCTTGACCTCCCC[A/G]GGCTCAGGAGATCTT | 27342 |
| rs575382953 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731418 | TGAACGCCTGGCTGG[C/T]AAATAAGGATCTTGG | 27342 |
| rs575383529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716762 | TCTATCATTTTGTTA[C/T]TTTCTGTTTGCTCTC | 27342 |
| rs575403561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758212 | CTGCAAAGTATTTTC[A/G]TTTTGCTTTTCTGAG | 27342 |
| rs575420176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805399 | TTTCACCAATCTGGT[A/G]AGTAAGTGAGTTCTT | 27342 |
| rs575428205 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705947 | GTCGCCCAGGCCGGA[C/G]TGCGGGCTGCAGTGG | 27342 |
| rs575438418 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758788 | CTCTTTTTATACTTA[C/G]AAGCAGCAGAATGAT | 27342 |
| rs575442623 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730150 | ACTTCCTCACGTCCA[C/T]GGAGAGTGCAACAGG | 27342 |
| rs575448227 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686113 | TGCGAAACCCCGTCT[C/T]TACTAAAATACAGAA | 27342 |
| rs575485366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804463 | GGCTTGGCCAGGCAC[A/G]GTGGCTCACGCCTGT | 27342 |
| rs575525617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754507 | CCAGCACTTTGGAAG[A/G]CCACAGTGGGCAGAT | 27342 |
| rs575530247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66685560 | CTTTCTGTAAGGATG[C/T]CTGACCCAGCTAATT | 27342 |
| rs575538534 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723385 | AGTTTATAATGTGAA[C/T]CTTTAACTTTTCACA | 27342 |
| rs575572051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807441 | CTTTGTAAAGTCTGT[A/G]TCTTCTACTTCCACC | 27342 |
| rs575585114 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime | RABGEF1 | GRCh38.p7 | 7:66712194 | AGCAGTGACATCCAA[A/C]CTGTATCAAGTCTTC | 27342 |
| rs575617965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800142 | TGAAATTCTATTGGA[A/G]AGGAAGTGGGTTAAC | 27342 |
| rs575624713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722786 | TAATTCTGCATTTCC[A/G]TATGAATTTTAGAAT | 27342 |
| rs575630070 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723135 | TGCCACGCCCGGCTA[C/G]TTTTTGTATTTTTAG | 27342 |
| rs575658200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767889 | AAGGAACTAAGATGC[C/T]GGCTTCTATCAGCAT | 27342 |
| rs575671523 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793478 | ATTTTTGAGCATTTC[A/G]GATTTTTTATTTTTG | 27342 |
| rs575761998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736980 | AATATATATATGTGC[C/T]GATGCACTGGGGCTT | 27342 |
| rs575764473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760037 | TTATCATATAGAGCA[C/T]AGGGCTAGTACAAGA | 27342 |
| rs575775252 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793472 | TTTGGGATTTTTGAG[C/T]ATTTCAGATTTTTTA | 27342 |
| rs575805542 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66682113 | CGCTGGCGGTGCCGG[C/G]GGGGCGGGGCAAGCA | 27342 |
| rs575810664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686903 | CTCGGCTCACTGCAA[A/G]CTCCGCCTCCCGGGT | 27342 |
| rs575821450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737625 | TTTAATTTTGCCAAG[A/G]AAAGTCTTTTTTAAA | 27342 |
| rs575831286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730521 | GTCTATGCAGATTAC[C/T]TGAGCTCATTCACAT | 27342 |
| rs575835395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742767 | GCGTGCCACCACACC[C/T]AGCTGATTTTTAAAT | 27342 |
| rs575838895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779876 | TCCTCCCTGCATACC[A/G]AACACCTGAGCTGTC | 27342 |
| rs575876172 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737926 | ATTTGCATAGCAGCA[C/T]AGCTGGCTCCCTCAT | 27342 |
| rs575918640 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736467 | AGCATTTTGGGCAAA[G/T]AATACAATGTGAGCA | 27342 |
| rs575943539 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691821 | CACTTTGGGAGACTG[A/C]GGCGGGAGGATCACT | 27342 |
| rs575947508 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726613 | CTCAAGTAATCCCCC[A/G]ACCTCAGCCTCCCAA | 27342 |
| rs575982586 | snp | G/T | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681520 | CCTCCCACCTCAGCC[G/T]CCCCAGTAGTTGGGA | 27342 |
| rs575985720 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712682 | TCACCATGTTACCCA[G/T]ATTGGATCTTGAATT | 27342 |
| rs575991015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732488 | AGGAGGCAAGTGGAG[A/G]TCCATATACCCAAGT | 27342 |
| rs575997676 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772924 | CTCAAAAAAAAATAA[A/T]TAAATAAATAAATAA | 27342 |
| rs576035013 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724050 | AGTTTCTGTTGGGCA[A/G]TAAATTTTCTCACCA | 27342 |
| rs576043455 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688411 | CATGATAATCCAACT[A/G]GATCTAATGGACATT | 27342 |
| rs576059208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781612 | TGCTGTGGTTCTACA[C/T]GTTACTTGGTGGTTT | 27342 |
| rs576107084 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709680 | CTCAGGAGCCTGAGG[A/C]AGGAGAATCGCTTGA | 27342 |
| rs576110863 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732124 | GTAGCTAGAACGCCC[A/G]GCTCACCAGGCCACC | 27342 |
| rs576114846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789614 | CGTGAACCCGGGAGG[C/T]GGAGCTTGCAGTGAG | 27342 |
| rs576135308 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686357 | TATGCCTATAATACC[A/G]GTGCTTTCGGAGGCC | 27342 |
| rs576220385 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748036 | AAATTTGGCTTTGCT[A/T]TTGAGTAGCCAATTA | 27342 |
| rs576221626 | snp | A/G | | | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756383 | GTTTGGTATATGTCA[A/G]AATTTTAAATGCACA | 27342 |
| rs576247665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694640 | TGACGTGGATGTCAC[A/G]ATACCCCGGCCAAAT | 27342 |
| rs576260585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712637 | CACCTCACCCAGCCA[A/G]TTTTTTGTATCGTTG | 27342 |
| rs576280467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761975 | AGAATCACTTGAACC[C/T]GGGAGGTAGCGAAGG | 27342 |
| rs576289756 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706274 | TAAATAAAACTGATA[C/T]GAACATTTTTATACA | 27342 |
| rs576293769 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693054 | AGCAGTGAGCCGGCT[A/G]GTCCCGTGGCCTTCA | 27342 |
| rs576338030 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802428 | TCCAGCAGAGATGGA[A/G]CGTATACTTAGCTCT | 27342 |
| rs576341653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768330 | GGGACACCAGTGTAT[A/G]TATCTTCTTTGTTAA | 27342 |
| rs576367618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775084 | TCCATCCTGTAGCAA[C/T]GTGAGACCTCAGACT | 27342 |
| rs576391145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787566 | GCCAGGCTGGTCATG[A/G]ACTCCTAGCCTCACA | 27342 |
| rs576400164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774100 | TTAATGGCATCACTA[C/T]TTACCAAGTTAGCTA | 27342 |
| rs576446213 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750228 | AAGTTGTATAGTCAT[G/T]AATGGACACTTTTTA | 27342 |
| rs576496153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739752 | AGCTGGGATTTTAAC[C/T]CAGGTCTATCTCACA | 27342 |
| rs576508203 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739223 | CCAAAGTGCTAGGAT[G/T]ACAGGCGTGAGCCAC | 27342 |
| rs576511359 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795399 | ATAACCTGTGAGTAC[C/T]TTTAGGCTTACTACC | 27342 |
| rs576529904 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795941 | GCCAGGAGTTCGAGA[C/G]CAGCCTGGCCAACAT | 27342 |
| rs576534859 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780087 | CTTTGGAAAAGTATG[G/T]GTGGGAGGGAGGCAT | 27342 |
| rs576572177 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743882 | GTGATTCTCTAGCCT[C/T]GGCCTCCCAAAGTGT | 27342 |
| rs576583772 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723802 | TCAGGCTGGTCTCGA[A/T]CTCCTGACCTCAGGT | 27342 |
| rs576585604 | snp | G/T | 0.0079259 | 0.062451 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746941 | GGTGTTAACAGGCAC[G/T]CGCCACCATGCTGAG | 27342 |
| rs576610816 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747900 | ATACGTGCGACATAC[C/T]GTTGGTAACATAACA | 27342 |
| rs576631456 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755181 | TGCCTGTAGTCCCAG[C/G]TCCTCTGGAGGCTGA | 27342 |
| rs576669047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745052 | AAAAAATTAGCCGGG[C/T]ATGGTTGCAGGCGCC | 27342 |
| rs576670712 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683676 | CTAACAGGGTGGAGT[G/T]AGGGAGAGGGGGGAA | 27342 |
| rs576691637 | in-del | -/CATTTGACAA | 0.00199481 | 0.0315187 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720144 | CTTGCAGAAAAGAAG[-/CATTTGACAA]CATTCAACATCCATT | 27342 |
| rs576701401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801459 | TATAGTTCCCCTGTC[A/G]TGCTAGCAAATACTA | 27342 |
| rs576753950 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692586 | AGAGATTGCACAGGA[A/G]GGTCAACAATCCTGA | 27342 |
| rs576756666 | snp | C/G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790322 | CAAGTTCCACCCTTA[C/G/T]GCGCATGAGGTCTTT | 27342 |
| rs576782769 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720395 | TAGAGACGGGGTTTC[A/G]CCATGTTGGCCAGGC | 27342 |
| rs576788418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694592 | TTGGCTCCCTATGGA[A/G]AACCAGCTGGAGGGG | 27342 |
| rs576801830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700862 | CAGGCCAGTGGGATG[C/T]GGGCTGCTGGCCCTG | 27342 |
| rs576803811 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707706 | AACAACAAAAAGAGT[A/C]TTGAAGTGGCTAAAT | 27342 |
| rs576809236 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788184 | GGGCGAGGTTGCTCA[C/T]ACCTGTAATCCCAGC | 27342 |
| rs576818355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719821 | TTCCTGTTTTCCTGT[C/T]ACAGTAGTAGGGTTG | 27342 |
| rs576835469 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742744 | CCCGAGTAGCTAAGA[A/C]TGCAGATGCGTGCCA | 27342 |
| rs576843920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737178 | TAGGCAATCCTCCCA[C/T]CTTGACCTCCCAAAA | 27342 |
| rs576846369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780806 | CCCTTTTTTGTTCTT[A/G]GTAATATGGTCCATG | 27342 |
| rs576862541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731979 | GGGGGAAGGCTGGAC[A/G]ATGATCTGGGGAGGA | 27342 |
| rs576909001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795322 | AACTAAGGAAAAGTC[C/T]GGCAACAATGGATAT | 27342 |
| rs576934297 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724783 | TCTGGTACTCCAATT[A/G]TATGTGTGTTGGATG | 27342 |
| rs576980361 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801339 | AGTGGTAATTACCTT[A/C]GGGGAAATGGGGTCC | 27342 |
| rs577060764 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706489 | ATCTCTGCTTACTGC[A/G]CCCTTTGCCTCCCGG | 27342 |
| rs577082503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759987 | CTAGACAAGCTGGAC[A/G]GTGTGGTTCAGTACC | 27342 |
| rs577116926 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767629 | TTTGGGAGGTGATTA[G/T]TTCATGAAAGTGGAG | 27342 |
| rs577126090 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774753 | CGATGGAGTGACACT[C/G]TGTCTCAAAAACAAC | 27342 |
| rs577127928 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767234 | TCTCAAACTCCTGCC[C/T]TCAGGTGATCCACCC | 27342 |
| rs577133308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788853 | CCAGCTACTAGGGAG[A/G]CTGAGGCAGGAGAAT | 27342 |
| rs577155124 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688292 | GCAAGAAAGGGTAGA[A/C]TTGAAGGGAAAAGAA | 27342 |
| rs577193110 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793364 | GCAGTTTTGTGCATG[A/T]AACAGTTTTGGCTGC | 27342 |
| rs577233424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713698 | TTCCCCTTTATTCCT[A/G]TTTTGAAAAGAGTTT | 27342 |
| rs577244091 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721138 | TGGCCAGGCTGCTCT[A/C]GAACTCCCGAGCTCA | 27342 |
| rs577252407 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788503 | TTGGGTTTCTCAATT[A/C]AGTTATTTTTATTTT | 27342 |
| rs577255332 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800039 | AAATTACAAAAAAAA[A/C]TCTTAATGGAGAGAT | 27342 |
| rs577265611 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66740962 | TCCCACATTCCGTCT[C/T]CGTCAGCGCCGCCTT | 27342 |
| rs577290236 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755088 | TCACGAGGTCAGGAT[A/T]TTGAGACCATCCTGG | 27342 |
| rs577321890 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697329 | GCGTGGCGTCTCACA[A/G]GTCTTGCATTTCAGG | 27342 |
| rs577359121 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719591 | AAGGAGGGAGTAATA[G/T]GAATCCCACAAAAAC | 27342 |
| rs577362945 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792111 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 27342 |
| rs577364561 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696900 | ACATGGTGCAGGTTC[C/T]CTTGGTGATGGTGGA | 27342 |
| rs577371582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748871 | TCTGCACTGTTTCAG[C/T]ACCTTATTGAAACCC | 27342 |
| rs577382330 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759224 | GTTCGAGGCTCTCAC[A/G]GGACATATTTATTCC | 27342 |
| rs577485637 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718742 | GTGGTCCATCCTGTA[A/G]TTTCTTTCTCAAAGC | 27342 |
| rs577497124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807907 | CAATCCTCCCACCTC[A/G]GCCTCCCAAAGTGCT | 27342 |
| rs577502092 | in-del | -/TTCTT | 0.00517822 | 0.0506191 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711586 | TATTTGTATACTCTA[-/TTCTT]TTCTTTTTTTTTTTG | 27342 |
| rs577522968 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803489 | CGCTGCCTCTCCAGC[A/G]GTGCTGTCACCACGT | 27342 |
| rs577554121 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714721 | CGGGCGGATCATGAG[G/T]TCAGGAGATCATGAC | 27342 |
| rs577591729 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802891 | AGATGAACAGGATGC[A/C]AGATGAAAGAACATT | 27342 |
| rs577592251 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810808 | CTTCCTAAGGATGGA[A/G]CCCAAAATTGCAGAG | 27342 |
| rs577600649 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763475 | AATAGTGCTTTGACT[C/G]TCTCTAACTTCACAT | 27342 |
| rs577618732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762914 | AGCAAGGGCCACAGC[A/G]TTCCTCACTTTGGAA | 27342 |
| rs577629668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725613 | TGCTGTTTTTGTTCC[A/G]TCCATGGCAATTTTA | 27342 |
| rs577639423 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750648 | TATAATATACACACA[C/T]ATAATGGTGCTTGAG | 27342 |
| rs577643280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771542 | GCAAAATCCAGTGTC[A/G]GGAAGCTTTTCCCCT | 27342 |
| rs577672857 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796119 | TCCAGCCTGGGCAAC[A/C]GATCGAGACTCTGTC | 27342 |
| rs577692741 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690964 | AGTGTGGTGGGGAGC[A/G]CCTATAATCCCAGCT | 27342 |
| rs577695871 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810258 | TCTGAACCTTTTTCA[C/G]GACATTTCAACCTCG | 27342 |
| rs577719524 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733787 | ACGGGCAGATCATTT[G/T]AGGTCAGGAGTTTGA | 27342 |
| rs577733633 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726129 | AGGGATGCCAGGCAC[A/G]GAGCCAGAATCCCAA | 27342 |
| rs577812600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684376 | TTGAACCCAGGAGGC[A/G]GAGGTTGTCTGAACC | 27342 |
| rs577861441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783096 | CTCTTCATTGTATGC[C/T]TTGTTGTGTTTATCA | 27342 |
| rs577864416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782552 | CGTAGCTCACTGCAG[C/T]GTCAAACTCCTGGGC | 27342 |
| rs577872523 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767302 | GCCACTGTGCCCAGC[C/T]GAGGTTTTTTTTTTG | 27342 |
| rs577941394 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768515 | TTTGTTTTCTAAACA[G/T]TTATTCCCAGAGCAA | 27342 |
| rs577954138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811538 | GGTTTTCTGGTTAAG[C/T]TATACCTAAAAATGA | 27342 |
| rs577963380 | snp | A/C/T | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681694 | TTTGGATCAAACGAT[A/C/T]GGCTTAAGACCCTTT | 27342 |
| rs577981777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692426 | AGTGCATTGAGTGAT[A/G]TTGGTGTGAGGTGGG | 27342 |
| rs577992507 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701884 | AATTTTTTTATTGAT[A/G]ACTGTTTTTAAAAAT | 27342 |
| rs577993688 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775530 | GACACTGAAATTGGG[C/T]TTGAGGGTCAGACAG | 27342 |
| rs577999334 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691954 | CCCAGCTACTGTGGA[C/G]GCTGAGGTGAGAGGA | 27342 |
| rs578015994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734590 | CGTGAGCCACCATGC[C/T]TGGCTAATTTTTTTT | 27342 |
| rs578034850 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729149 | TAGATATGGGGTTTC[A/T]CTGTGTTAGCCAGGA | 27342 |
| rs578055406 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784694 | CAGTGGACTTGTGTC[A/G]AAATAATTTTTAGAT | 27342 |
| rs578089698 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784182 | GCAACCATTGTTAGG[A/C]CAGTGGCAGTAATTT | 27342 |
| rs578100709 | snp | A/T | 0.0123036 | 0.0774623 | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740400 | CGCGGCCGCAGCCCC[A/T]GGAGTCGCCGCGGAG | 27342 |
| rs578109388 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697440 | GGATGGGTCAAACCG[A/T]CGTCTCTCCCTTCAC | 27342 |
| rs578172979 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696910 | GGTTCCCTTGGTGAT[A/G]GTGGATGCAGGAAGG | 27342 |
| rs578196402 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790896 | CTGTATCTGCTCAGA[C/G]TCTAGTGACATCAAA | 27342 |
| rs578199471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703000 | TTTTGAGAAGGAGTC[C/T]CGCTCTGTCGCCGCC | 27342 |
| rs578213521 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757324 | ATTTCATGTACCTAT[A/C]TAGCTTATTTCACAT | 27342 |
| rs578261236 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796620 | TTTGTCGAGACAGAA[C/T]ATCACTCTGTCGTCC | 27342 |
| rs745316956 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726716 | ATGGTCTAAAATGGA[A/C]TGCGAGGTCAGGTGC | 27342 |
| rs745360926 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766166 | ACGTGGCGAAACACC[A/G]CCTCTACAAAAAAAT | 27342 |
| rs745362949 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773921 | TCCGGCCGCCTTGGC[C/T]TCCCAGTGTGCTGGG | 27342 |
| rs745374074 | snp | A/G | 5.02365e-05 | 0.00501156 | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66799413 | GGTGAAGGCGATCAC[A/G]GGTCAGTGAAACCAA | 27342 |
| rs745376058 | snp | A/G | 1.64732e-05 | 0.0028699 | missense | RABGEF1 | GRCh38.p7 | 7:66805227 | TCTTCAATGCCATCA[A/G]GATCACCAAGAATGA | 27342 |
| rs745386323 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684927 | GGCGTGAGCCACTGT[A/G]TCTGGCCTAAATTTT | 27342 |
| rs745391590 | snp | C/G | 3.51457e-05 | 0.00419185 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775201 | GGAGAATATCTAGGT[C/G]ATTCTAATCCTCTCT | 27342 |
| rs745413036 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714499 | AGAGGTTTGGGAATT[C/T]TACACATCTTTTCAA | 27342 |
| rs745425440 | in-del | -/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788104 | GGGCAGGCTCTACTT[-/C]CTCAAAGTACCTACC | 27342 |
| rs745437331 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778270 | GTTTTTATGCCATAC[A/G]TAGCAGCTTGGTAGC | 27342 |
| rs745453772 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775547 | TGAGGGTCAGACAGT[A/G]TATGAAATCAATACT | 27342 |
| rs745462383 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781027 | CTGTTTATAGCACGT[-/A]ATATTTAATGTGATT | 27342 |
| rs745493174 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709070 | TCGCCCAGGCTAGAG[C/T]GCAATGGCACAATCT | 27342 |
| rs745536360 | snp | C/G | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680528 | GGATTACAGGCGTGA[C/G]CCACCGCACCCAGCC | 27342 |
| rs745539070 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733862 | ATAAAAAAATTAGCC[A/G]GGTGTGGTGGCACAC | 27342 |
| rs745561522 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683731 | ACAAGGAGGTGCTTA[C/T]TTATTTATTTATTTA | 27342 |
| rs745599936 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731678 | GCTATGATTGTGCCA[A/C]TGCACTCCAGCCTGG | 27342 |
| rs745623793 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761050 | CTTTCAACAAAGAAT[C/T]GAGAACCTGTGATAT | 27342 |
| rs745659016 | snp | C/T | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758229 | TTTGCTTTTCTGAGA[C/T]GAAACTGGTTTGCAT | 27342 |
| rs745659091 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742750 | TAGCTAAGACTGCAG[A/T]TGCGTGCCACCACAC | 27342 |
| rs745679566 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692427 | GTGCATTGAGTGATA[C/T]TGGTGTGAGGTGGGG | 27342 |
| rs745696195 | in-del | -/GAGAGA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737053 | ATATATGAGGGGGGA[-/GAGAGA]GAGAGAGAGAGAGAG | 27342 |
| rs745713514 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763341 | GGCAGAATTCATTTT[C/T]ATGTGGTGAAGGTCT | 27342 |
| rs745724893 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719369 | CACCAAGCCCAGCTA[A/G]TTTTTATATATATTT | 27342 |
| rs745725666 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786371 | GTATAATGCTTTACT[A/G]TGCAACACACTTCTC | 27342 |
| rs745735948 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775773 | CAGAAATGGTGATTT[A/C]TAGGCTTGATAGTCA | 27342 |
| rs745753763 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762043 | TGGGCAACAGAGCGA[C/G]ACCCTGTCTCAAAAA | 27342 |
| rs745792782 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701816 | TGGATACAAGTTCTT[C/T]ATCAGATATATGGTT | 27342 |
| rs745857142 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744262 | TAGATGTTTGAAATG[A/G]TGGCTCACGCCTGTA | 27342 |
| rs745867859 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723029 | GCTGGCGTGCAATGG[C/T]GTGATCTTGGCTCAC | 27342 |
| rs745908873 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768127 | TCTAGAGGAAATACC[C/G]AGGAGAGGGATTGCA | 27342 |
| rs745916642 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796034 | CCCAGCTACTCGGGA[G/T]GCCGAGGCACAAGAA | 27342 |
| rs745918746 | snp | A/G | | | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66809050 | AATGTATAAGAACTT[A/G]GATCTCTTGTCTCAG | 27342 |
| rs745950257 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751271 | CCTGACCTCAGGTGA[G/T]CCGCCTGCCTCGGCC | 27342 |
| rs745965471 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712005 | TAATTACTTATAGTA[A/C]GTCCTAAATTCAGGT | 27342 |
| rs745980900 | snp | C/G | 1.64789e-05 | 0.0028704 | missense | RABGEF1 | GRCh38.p7 | 7:66808970 | CGCTACATGTCTGGC[C/G]AGACCTCTCCCAGGA | 27342 |
| rs745997383 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802298 | ACAGGATGGTTCCCT[-/A]CAACAAAGAATTATT | 27342 |
| rs746024205 | in-del | -/TA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731665 | GAGACTGCAGTGAGC[-/TA]TGATTGTGCCACTGC | 27342 |
| rs746044071 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737976 | ATGAGGCCGCTCCGG[A/T]CTATTTTAAAGCTGC | 27342 |
| rs746048718 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778852 | CAGGCACGGTGGCTC[A/T]GGCCTATAATCCCAG | 27342 |
| rs746088503 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721783 | GACCAGCTTGGCCAA[C/T]GTGGTAGAACCCCGT | 27342 |
| rs746100246 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780957 | TTCTTACAGACAGCA[C/T]GAAGTGGGGTCTTGT | 27342 |
| rs746112234 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796678 | GCTCACTGCAACTCT[G/T]CCTCCCAGGTTCAAG | 27342 |
| rs746140944 | snp | C/T | 0.00034949 | 0.0132145 | intron-variant, missense | RABGEF1 | GRCh38.p7 | 7:66783732 | AAACCAGCATTGAAA[C/T]GGATAGAGTGTCTAA | 27342 |
| rs746171677 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729442 | CTCCCGTCTATTCTC[C/T]TCTCCAACCTCACTT | 27342 |
| rs746200358 | in-del | -/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706904 | CTCCTGCCTCAGCCT[-/C]CCGAGTAGCTGGGAC | 27342 |
| rs746207790 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802102 | CATTCTGTAGAGACA[A/G]AGTTTCATCATGTTG | 27342 |
| rs746222154 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770231 | TAAATTAATAAGATC[C/T]CCAAGATATAGGGCT | 27342 |
| rs746248827 | snp | G/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739755 | TGGGATTTTAACCCA[G/T]GTCTATCTCACAGCC | 27342 |
| rs746252456 | snp | A/T | 0.000115715 | 0.00760553 | missense | RABGEF1 | GRCh38.p7 | 7:66797422 | AGATTGAAAAGTACA[A/T]CATGACTCGTCTCTA | 27342 |
| rs746312786 | snp | C/T | 1.81168e-05 | 0.00300966 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799287 | ATGGCCACAGTTTAT[C/T]CTTGGAGCTCTTGTT | 27342 |
| rs746336774 | in-del | -/G | 2.80187e-05 | 0.0037428 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797328 | AAAAAAAAAGAGAGA[-/G]AAAAAATATATATAT | 27342 |
| rs746362789 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690520 | AAGAGTTCAAGACCA[A/G]CCTGGGCAACATAGT | 27342 |
| rs746367467 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728275 | ATTAGCTAAGCTTGG[G/T]GGGGCCACTGGGTCC | 27342 |
| rs746409812 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759195 | CCCAGGGCTGCCCCC[A/G]GGTTTCGTAATTCGT | 27342 |
| rs746440774 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688163 | ATAGGTTTTAAGCCA[A/G]CAATGGTTATGAGAG | 27342 |
| rs746456799 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716015 | CCTAGCTGATTTTCT[A/G]TCTGTTCTGTCCATT | 27342 |
| rs746482102 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800865 | GTGTGACCCATCAGT[C/G]GTGAAAGTAGAGGTG | 27342 |
| rs746488050 | snp | A/C | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754146 | AGCTGGGACTACAGG[A/C]GCCCTCCAACACGCC | 27342 |
| rs746512276 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768194 | TTATATTTACTGTAC[A/T]GGACAGTTAACAAAT | 27342 |
| rs746515454 | snp | C/T | 1.67508e-05 | 0.00289398 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775413 | TGTTCTGATACTCTT[C/T]TTTTTCTTCTCTGCC | 27342 |
| rs746515733 | snp | C/T | 1.65655e-05 | 0.00287793 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805420 | GTGAGTTCTTGGTGT[C/T]GTGGAGAAGGACTAG | 27342 |
| rs746572475 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735656 | GTTATTGTGAGATCT[A/G]GTGGTTTAAAATGTG | 27342 |
| rs746631572 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697418 | ATAATTTCTGTGTTG[C/T]CACCAGGGATGGGTC | 27342 |
| rs746684209 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788110 | GCTCTACTTCCTCAA[A/G]GTACCTACCCTTTAA | 27342 |
| rs746712792 | snp | C/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758266 | CCTTAAGAAAGAACA[C/G]TAATAGTTCTGTGAG | 27342 |
| rs746723130 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686121 | CCCGTCTCTACTAAA[A/G]TACAGAAAACTTAGC | 27342 |
| rs746725863 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721987 | TGAGACCCCCCCTCC[A/G]TCTTTTCAAAAAATC | 27342 |
| rs746729915 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808600 | CTTGGGGACTATATC[C/T]TGGGTGGGGATAGCA | 27342 |
| rs746749965 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733084 | TGGAGTCCTGGCCCC[C/T]AAGGCATTGGTGCTC | 27342 |
| rs746791576 | in-del | -/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727479 | TCTGCTCCTACCCTG[-/C]CCTGCCTGGTCAGTT | 27342 |
| rs746809254 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745852 | ATAATACCAGTGCTT[C/T]GGGAGGCCAAAGTGG | 27342 |
| rs746818415 | in-del | -/TATATCTTGATCTTTTC | 9.72113e-05 | 0.0069711 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797338 | GAGAGAAAAAATATA[-/TATATCTTGATCTTTTC]TATATCTTGATCTTT | 27342 |
| rs746827902 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744284 | ACGCCTGTAATCCTC[C/G]CACTTTGGGAGGCCA | 27342 |
| rs746842959 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764782 | CAGAAGACGTATGGG[-/T]TTATTTCTGGAATCT | 27342 |
| rs746887716 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752611 | ATAAATGGACATTTT[C/T]GTAATTGTGGTGTTT | 27342 |
| rs746888016 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764073 | CACAATGGCTGTACC[A/G]TTTTACATTCCTACA | 27342 |
| rs746935502 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692747 | TGATGTCCTACATCC[C/G]CCTGAGCCTAGGATG | 27342 |
| rs746966622 | snp | C/G | | | utr-variant-3-prime | RABGEF1 | GRCh38.p7 | 7:66809349 | TTACTACACTCAACT[C/G]ATTGGGATCTAGAAT | 27342 |
| rs746977684 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763392 | GGCTGTCAGCCAGAA[G/T]TCATTCTCAGCTTCT | 27342 |
| rs746979157 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693362 | AATACTGTTGCACAA[A/T]CTCCGTCTCTCCCCT | 27342 |
| rs746993908 | snp | C/T | 8.23621e-05 | 0.00641672 | missense | RABGEF1 | GRCh38.p7 | 7:66805248 | CCAAGAATGAGCCGG[C/T]GTCAGCGGATGACTT | 27342 |
| rs747024556 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798212 | CTTTCACTGGCATTG[G/T]ATTGATGACATTTCC | 27342 |
| rs747046892 | snp | A/G | 4.94629e-05 | 0.00497283 | missense | RABGEF1 | GRCh38.p7 | 7:66809090 | CGACAAGAAAGGATC[A/G]TGAATGAAGCCAAGA | 27342 |
| rs747067341 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781436 | TTACATAGGTATATA[C/T]GTGCCCTGGTGGTTT | 27342 |
| rs747082788 | in-del | -/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751650 | TACTCCTAGCAGGTA[-/C]CCACCTAAGACTTTC | 27342 |
| rs747096372 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688682 | TGAAGATGAAATCAT[A/G]CAGGAAATTAGAAAA | 27342 |
| rs747098701 | snp | A/G | 2.88114e-05 | 0.00379537 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783887 | GAGTTTTGGTTTGAG[A/G]AAAGGTCTTAGAGAT | 27342 |
| rs747099760 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729547 | AACCTCACCTTTATC[A/C]TCACCTTCATCCTTA | 27342 |
| rs747100288 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699834 | CTTCAACCTGAGTGA[C/T]AGAGAGAGACCCTGT | 27342 |
| rs747107843 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738167 | CTGGGATTACAGGTA[C/T]AGGCCACCACCTGGC | 27342 |
| rs747119647 | snp | A/G | 1.64876e-05 | 0.00287116 | missense | RABGEF1 | GRCh38.p7 | 7:66809153 | GGAATTGCAAGAGAA[A/G]TTCAAGACATCGTTG | 27342 |
| rs747139846 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729817 | TGCCTTGTGGAGCAC[A/G]TCTGCCTGTGAGCTG | 27342 |
| rs747186146 | snp | A/G | 4.94222e-05 | 0.00497078 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66795573 | CAATGTGGCCGAAAG[A/G]ATGCAAACTCGTGGG | 27342 |
| rs747213965 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741329 | GGAGTTGGGAGGGGA[C/T]TTGAAGCCTGTGGTC | 27342 |
| rs747236382 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712154 | TTTGATCTGTGTTTT[A/G]TTAAATCTACAGATC | 27342 |
| rs747245038 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740119 | GACCACAGGTGCCCG[C/T]CATCATGTCCGGCTG | 27342 |
| rs747265555 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713290 | GGGACTACAGGTGCC[C/T]GCCACCATGCCCAGC | 27342 |
| rs747309381 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719512 | CAAAATTTTTTTTAT[A/G]TAAATCTTTCTGATA | 27342 |
| rs747335736 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805126 | TGGGAAATATTGTCT[C/T]TTCTGCTTTGTAGAT | 27342 |
| rs747359943 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793552 | TATAGTTTCTTCTAA[A/G]TTAAGTGCTAAAATT | 27342 |
| rs747385449 | snp | C/G | 1.70839e-05 | 0.00292262 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799311 | TCTTGTTTACTGTCT[C/G]TCTCTCTTTAGAGCC | 27342 |
| rs747389827 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759866 | GGGGACACAGTTCCA[A/G]ACCATATCACATAGG | 27342 |
| rs747401224 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708193 | TTAATTCCTTGTTGT[G/T]ACTTTTACTATATAT | 27342 |
| rs747401548 | in-del | -/TAACTC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718910 | CCCTCCCTAGTCCTT[-/TAACTC]TAAAGCCAGGGCTTC | 27342 |
| rs747404062 | snp | A/G | 3.51074e-05 | 0.00418957 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772085 | GGCGGAGCGGTAAAA[A/G]GACTTAACTAGGGGC | 27342 |
| rs747414688 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771382 | CTGATTTTGTTATCC[A/G]CCCTCCTCAGCCTCC | 27342 |
| rs747424773 | snp | A/G | 0.000141213 | 0.00840158 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773934 | GCCTCCCAGTGTGCT[A/G]GGATTACAGGCGTGA | 27342 |
| rs747427039 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748745 | TTACCTGATGATTAC[A/G]CTTTATACCTTCACT | 27342 |
| rs747470654 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734514 | TTGGCCAGGCTGGTC[G/T]TGAATGCCTGACCTC | 27342 |
| rs747498448 | in-del | -/CATA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749111 | AAGCCACCTCACCTC[-/CATA]CAGAGATGGGCTGAG | 27342 |
| rs747502319 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718798 | ACACATGCAGCTCAG[C/G]GGTGAGCTGAAGAGT | 27342 |
| rs747512941 | snp | A/G | | | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760853 | AGGCTGGTCTTGAAC[A/G]CTTGACTTTGAGCCA | 27342 |
| rs747538319 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730301 | AAGTCACTCACTGTT[G/T]CTGCTGAGCGCCAGC | 27342 |
| rs747654464 | snp | A/G | 1.66222e-05 | 0.00288285 | intron-variant, missense | RABGEF1 | GRCh38.p7 | 7:66783714 | GTCCTTCCATAAACC[A/G]GCAAACCAGCATTGA | 27342 |
| rs747656334 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759109 | CCACCACCATAGTCA[A/G]GATACAGAACTATTC | 27342 |
| rs747686015 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777009 | TACCAGAGGCACGTG[A/G]TGAGGATTCAGTGAG | 27342 |
| rs747699551 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793956 | TTATTCATGTTCTTC[A/T]ACTGTGACATCCTTA | 27342 |
| rs747716411 | snp | A/G | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66738877 | ATAGCAATTACCACC[A/G]TCCAAGGTACTACTG | 27342 |
| rs747716453 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802001 | TGCAGCCTTGACCTC[A/G]CAGGCTCAAGCGATC | 27342 |
| rs747721653 | in-del | -/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694384 | GAGAAGATGGAGCGA[-/G]GATCAGTGAGGCACC | 27342 |
| rs747740985 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717291 | ACTTGTAAAATGTAG[G/T]AACCTGGCTATCATG | 27342 |
| rs747761332 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687974 | CCTGTAATCCCAGCT[A/G]CACGGTAGGCTGAGG | 27342 |
| rs747804702 | snp | A/G | 1.65168e-05 | 0.00287369 | missense | RABGEF1 | GRCh38.p7 | 7:66797443 | CTCGTCTCTATAAAT[A/G]TGTATTCTGTCCAGA | 27342 |
| rs747822662 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718206 | AAAAAAATATTAGGC[A/G]TGGTGGTGCACATCT | 27342 |
| rs747824299 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791849 | CCAGGTGCGGTGGCT[C/T]ACGCCTGTAATCCCA | 27342 |
| rs747854681 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775867 | TATTGAGAACATATA[A/G]GAAAAGGCCCAAGTT | 27342 |
| rs747875520 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724827 | CTATAGGTCACCAAG[G/T]CTCTGTTAAAATTTT | 27342 |
| rs747878194 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764223 | CTTCCTTGATGACTG[A/G]TGATGTGGAACATCT | 27342 |
| rs747879300 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745995 | TACAGGCCAAACATC[A/T]TGAAAATCTTATTAA | 27342 |
| rs747924980 | snp | C/G | 1.66158e-05 | 0.0028823 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805435 | TGTGGAGAAGGACTA[C/G]GAAGGTGGTGGTTTT | 27342 |
| rs747946156 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727199 | GGTTGGCTGTAGAAT[C/T]GGGATCTTTGCTGAC | 27342 |
| rs747982026 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683256 | GTGCTGGGATTAGAG[A/G]CGTGAGCCATTGCGC | 27342 |
| rs748004020 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810213 | GCCTCCATAATATAC[A/G]TTTGACTTTGCAAAC | 27342 |
| rs748012728 | in-del | -/AAAAAAAGAA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779506 | GAGGCCCCCATCTTT[-/AAAAAAAGAA]AAAAAAATTAAAAAA | 27342 |
| rs748065435 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694035 | GCTGGTCTCGAACTC[C/G]TGGCCTCAAGTGATC | 27342 |
| rs748068447 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723602 | TGTTTTTTTTTGAGA[C/T]GGAGTCTCACTCTTG | 27342 |
| rs748069838 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780256 | CATAGTCAGTTGTTA[A/G]TAGTCAACAGCTCAG | 27342 |
| rs748083391 | snp | C/T | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681441 | TCTCGCTCTGCTCTG[C/T]CACCCGGGCTGGAGT | 27342 |
| rs748095465 | in-del | -/TTA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702690 | GTATGAAGTGGTGTC[-/TTA]TTGTGGTTTTCACTT | 27342 |
| rs748144913 | snp | A/G | 1.68476e-05 | 0.00290233 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775426 | TTTTTTTTCTTCTCT[A/G]CCTGAGTGAGACACA | 27342 |
| rs748160894 | snp | A/G | 3.29484e-05 | 0.00405871 | missense | RABGEF1 | GRCh38.p7 | 7:66795584 | AAAGGATGCAAACTC[A/G]TGGGAAAGGTAACAC | 27342 |
| rs748165911 | snp | C/T | 1.64822e-05 | 0.00287068 | stop-gained | RABGEF1 | GRCh38.p7 | 7:66808940 | TCTTTGAATCTAAGT[C/T]AGGAGGATTTTGATC | 27342 |
| rs748211749 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719724 | AAACCATGGCTTGTG[A/G]GGCCAAACCAGACTA | 27342 |
| rs748239193 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741432 | CGTCTGGGAGGAGAG[A/C]CGAGGGATGCCCATC | 27342 |
| rs748318404 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66805289 | CTCATCTACATTGTT[C/T]TGAAGGGCAACCCCC | 27342 |
| rs748323083 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784046 | ACTCAGTGGTGTTTG[A/G]ATCATCTTTGTGTGG | 27342 |
| rs748352546 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687523 | AAAGAAAAGAAGAAG[A/G]AGAATATAGGCTATG | 27342 |
| rs748372270 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700059 | GGGACCCCCAAGTTC[C/T]TGGCCCAGAGCCCCT | 27342 |
| rs748397226 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773452 | ATTTTTGTTTCTATT[C/T]CTTACTGCTTTTAAT | 27342 |
| rs748397570 | snp | C/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760099 | TCTAACCCAGCTGAC[C/G]AAGCAGGCCCGTCTG | 27342 |
| rs748401099 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710490 | GGTTGTACCATTTTG[C/T]GCTCCCTCTAGCATT | 27342 |
| rs748429607 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742844 | ACTCCTGCACTCAAG[C/T]AATCTTCCTGCCTCA | 27342 |
| rs748470238 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689982 | CAAAAACTTGAAGAG[A/G]AGGAAATACTTTCTA | 27342 |
| rs748488422 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794582 | ATAAAAATTATCAAG[C/T]CCAATGTTGTAAGGG | 27342 |
| rs748505479 | snp | C/G | 1.76805e-05 | 0.0029732 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775195 | AACCTTGGAGAATAT[C/G]TAGGTCATTCTAATC | 27342 |
| rs748514866 | in-del | -/AAAAAAAA | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739658 | CAGAGTGAGAGTCTC[-/AAAAAAAA]AAAAAAAAAAAAAAA | 27342 |
| rs748522060 | snp | C/T | 1.65416e-05 | 0.00287586 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66775296 | CCAATCCCTCACATT[C/T]TCCAAGTTTGAAGAA | 27342 |
| rs748539876 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749002 | GCTCTTGGTAGGTGA[C/T]ATCAGGCCTTCAGGC | 27342 |
| rs748569918 | in-del | -/AA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796153 | AAAAAAGAGAGAGAG[-/AA]AGAGAAAAACTTATT | 27342 |
| rs748580166 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749577 | CTGAGGCAGGAGGAT[A/T]GCCGGAGGTCAGGTA | 27342 |
| rs748594669 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780624 | AATCACCTCTCTGTC[A/C]ATTACTAAATGAGGA | 27342 |
| rs748601177 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806822 | CTAATGTTTGTATTT[G/T]TAGTAAAGACGGGGT | 27342 |
| rs748619496 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730067 | TGCCATAGACTCAGG[A/G]TGGCCTCCAAAAGTC | 27342 |
| rs748622619 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731782 | GCCACAGTCATGCCT[A/G]CCTCACCTTCATCTA | 27342 |
| rs748660320 | in-del | -/AAAAAA | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739660 | GAGTGAGAGTCTCAA[-/AAAAAA]AAAAAAAAAAAAAAA | 27342 |
| rs748668728 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720905 | TGAAATTTTAAAAAC[A/G]AAGCCATTATTATTA | 27342 |
| rs748704918 | snp | C/G/T | 4.94762e-05 | 0.00497354 | missense, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66809164 | AGAAGTTCAAGACAT[C/G/T]GTTGAGAAATACCCA | 27342 |
| rs748736401 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735348 | CCTTAGACTATGTTT[C/T]ATGGAAGACTTTATA | 27342 |
| rs748758436 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709286 | ATTATAGGTGTGAGC[C/T]ATCGTGCTCTGCCTG | 27342 |
| rs748773275 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777237 | TTTATGATAACAGAT[G/T]AAATAGTAAAACAAG | 27342 |
| rs748818810 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792003 | TGTAGTCCCAGCTAC[C/T]CGGGAGGCTGAGGCA | 27342 |
| rs748826677 | snp | C/T | 1.66543e-05 | 0.00288563 | missense | RABGEF1 | GRCh38.p7 | 7:66799330 | CTCTTTAGAGCCCTG[C/T]GCTGGGTTACGCCTC | 27342 |
| rs748837037 | in-del | -/TAGAGTAAAACATT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784815 | GGTATTTTTTCTCTC[-/TAGAGTAAAACATT]TAGAGTCAAAACAAG | 27342 |
| rs748861414 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696306 | TAATCTCAAGCAATC[C/T]GCCTGCTTCAGCCTC | 27342 |
| rs748867069 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725339 | AGAAGCTTCACTCCC[C/T]TTAGCCCTTGTCCCA | 27342 |
| rs748969906 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778074 | AGGTAAATTTTGCAT[C/T]TCACACTGATTACTT | 27342 |
| rs749013391 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694259 | AGTAAAGGGTGCCAC[A/G]GGAATGGGAAAGATC | 27342 |
| rs749021108 | snp | A/G | 6.59196e-05 | 0.00574068 | missense | RABGEF1 | GRCh38.p7 | 7:66808956 | AGGAGGATTTTGATC[A/G]CTACATGTCTGGCCA | 27342 |
| rs749022189 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734399 | CTCTTTGAGCCTCTG[C/T]TTCCTCGTCTATGAA | 27342 |
| rs749029470 | snp | G/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755152 | ACAAAAAATTAGCTG[G/T]GCGTGGTGGCAGGTG | 27342 |
| rs749032698 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707922 | TTTTCTGACATTAAT[A/G]TAGCCACTCTAGCTC | 27342 |
| rs749037718 | snp | A/G | 1.66233e-05 | 0.00288295 | intron-variant, missense | RABGEF1 | GRCh38.p7 | 7:66783722 | ATAAACCGGCAAACC[A/G]GCATTGAAACGGATA | 27342 |
| rs749060781 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799494 | TATTCATCTATACAT[C/T]TGTAAAATGCAGATT | 27342 |
| rs749070957 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780784 | CCTCTTTTTTATGAT[G/T]AGATGCCCCTTTTTT | 27342 |
| rs749099647 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701400 | CCAGCTACTAGGGAG[A/G]CTGAGATGGGAGGAT | 27342 |
| rs749126595 | snp | C/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739074 | TCCTGCCTCAGCCTC[C/T]CAAGTTGCTGGGATT | 27342 |
| rs749168291 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726654 | TTACAGGCATGAGCC[A/G]CTGCACCCAGCCCAA | 27342 |
| rs749171763 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787580 | GAACTCCTAGCCTCA[A/C]ATGATCCGCCCACCT | 27342 |
| rs749202256 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683549 | GGAGTGTGAGCTAAG[A/G]TGGAGCACCGAGGAA | 27342 |
| rs749203296 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730919 | TATAGCCCCACTTTT[C/T]AGAGGGAGGCACAGA | 27342 |
| rs749204755 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742554 | CTAACAGGGTGGAGT[G/T]AGGGAGAGGGGGGAA | 27342 |
| rs749205928 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713419 | AGGCTTGAGCCACTG[C/T]GTCTAGCCCAACCTG | 27342 |
| rs749229566 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741668 | CTGGAGAGCTGCTTT[A/C]CCCCCTCTAAACCTA | 27342 |
| rs749261605 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786152 | ATCATTTCTGTTTTC[C/T]CCAAGCCCTGTATAT | 27342 |
| rs749313803 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774751 | GGCGATGGAGTGACA[C/T]TCTGTCTCAAAAACA | 27342 |
| rs749334501 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764015 | AAATTGCTGGTTTCT[A/G]TGGTAATATTGTTTA | 27342 |
| rs749357437 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709443 | TAGTGCTATCTACAT[A/T]AAATATTCAAATCAG | 27342 |
| rs749373528 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761235 | ACTATCTACCAGGAG[A/G]TAGTGTCAGATCACA | 27342 |
| rs749377223 | in-del | -/AT | 0 | 0 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797333 | AAAGAGAGAGAAAAA[-/AT]ATATATATATCTTGA | 27342 |
| rs749378465 | snp | C/G | 1.66546e-05 | 0.00288566 | missense | RABGEF1 | GRCh38.p7 | 7:66797386 | CAGTGCCTCCAGAAA[C/G]AGTCGAGAAGATAAT | 27342 |
| rs749395792 | snp | A/C | 1.77391e-05 | 0.00297813 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66771888 | GTTTGTTCAGTGGTT[A/C]GCAGGAAGAAGATGA | 27342 |
| rs749407034 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721693 | TTAATTTAGGCTGGG[A/T]CCAGTGGCTCACGAC | 27342 |
| rs749409352 | in-del | -/AC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705445 | CATCTCGAAAGAAAG[-/AC]AGAGAGAGAGAGAGA | 27342 |
| rs749438033 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765695 | GATCATGTCACACAG[C/G]TCCATCATTCAAGAG | 27342 |
| rs749510942 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761919 | AGCTGGGCATGGTGG[C/T]AGGCACCTATAGTAC | 27342 |
| rs749530043 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808315 | CCGCCTCCCAGGTTC[A/G]AGCAATTCTCCTGCC | 27342 |
| rs749557513 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724391 | TTTGAGACGGAGTCT[C/T]GCTCTGTCACCAGGT | 27342 |
| rs749602838 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810155 | CTCTGATGGTGAGAG[A/G]TGACGGGGTCCCTCA | 27342 |
| rs749603235 | snp | A/G | 3.29843e-05 | 0.00406092 | missense | RABGEF1 | GRCh38.p7 | 7:66809168 | GTTCAAGACATCGTT[A/G]AGAAATACCCACTGG | 27342 |
| rs749612088 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727758 | GAGTGGCAGGCTGCC[C/T]GTGGATAATGGAAAA | 27342 |
| rs749668937 | snp | C/T | | | intron-variant, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811533 | ACAGAGGTTTTCTGG[C/T]TAAGCTATACCTAAA | 27342 |
| rs749698494 | snp | C/T | 1.68542e-05 | 0.0029029 | missense | RABGEF1 | GRCh38.p7 | 7:66809256 | ATAAACTTCCTCCAC[C/T]ACTGCAACCTCAAGT | 27342 |
| rs749733059 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731962 | CTCCCCCCAGGGCCC[A/G]TGGGGGAAGGCTGGA | 27342 |
| rs749746845 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786453 | CTATCTCCTGGACTG[A/G]AGCACAATAGCGCAG | 27342 |
| rs749755377 | snp | C/T | | | intron-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758451 | ATTGTGCATTCTTTA[C/T]GCCCAGGTTGCTCAA | 27342 |
| rs749841260 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768285 | ATCCTTGACTGCACA[C/G]TATGTAGCAAAGGCC | 27342 |
| rs749856269 | snp | G/T | 0.000381898 | 0.0138132 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796919 | TTTTAAGCGTATTTT[G/T]AAATATAACATTCTT | 27342 |
| rs749908268 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697291 | ATGGGGCCTCAGCCT[C/T]CATGTGCTGTAGGGG | 27342 |
| rs749913944 | snp | A/T | 2.12827e-05 | 0.00326204 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797345 | AAAAATATATATATC[A/T]TGATCTTTTCTCTGT | 27342 |
| rs749920854 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721984 | TAGTGAGACCCCCCC[-/T]CCGTCTTTTCAAAAA | 27342 |
| rs749990110 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768105 | TGTAAATAGCAATTT[G/T]TATTTCTCTAGAGGA | 27342 |
| rs749992713 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745725 | AATGAGCCGAGATTG[C/T]GCCACTGCACTCCAG | 27342 |
| rs750015887 | snp | C/G | 3.71223e-05 | 0.0043081 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771852 | AGTAGAATGATAATT[C/G]ATTTTCAACAGCACT | 27342 |
| rs750024339 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805535 | GAAGCTCACTTTGCA[C/T]CAGGGAGCACAAGGA | 27342 |
| rs750046457 | snp | A/G | 1.64781e-05 | 0.00287033 | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66805360 | CAATCCAAGCCGACT[A/G]ATGACTGGAGAGGAT | 27342 |
| rs750050742 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721377 | GAAGTCAGAAGTCCA[A/G]AGTCAGTCTGTCTGA | 27342 |
| rs750068228 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737219 | ACAGTATTTATTTAA[C/T]TTTTAGGTGTTTTTT | 27342 |
| rs750129508 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796185 | GGAAGGCTTTGCTAA[A/G]TGAATTTTCCATCTT | 27342 |
| rs750188605 | in-del | -/TT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691546 | TTACAATGGTTTGAC[-/TT]GGGATTTTTTCAACT | 27342 |
| rs750214968 | snp | A/C/T | 3.29697e-05 | 0.00406005 | missense | RABGEF1 | GRCh38.p7 | 7:66809145 | GGACAGATGGAATTG[A/C/T]AAGAGAAGTTCAAGA | 27342 |
| rs750234062 | in-del | -/TTTG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773666 | TGCTTGTGCTTTTTG[-/TTTG]TTTGTTTGTTTGTTT | 27342 |
| rs750250668 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704103 | AATTGTTATTGCAAG[C/T]GTATAGAACAGAGTT | 27342 |
| rs750277868 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686091 | AGAGACCAGCCTGGA[C/T]CAAGACTGCGAAACC | 27342 |
| rs750311989 | in-del | -/AG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796405 | AAAAATGAAAGGATA[-/AG]TTTCATCAGCATTCA | 27342 |
| rs750323189 | snp | A/G | 6.59163e-05 | 0.00574054 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795634 | GCGGGTATTGCACAG[A/G]GATGACTGCTCAGTC | 27342 |
| rs750335390 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712585 | AAGGGATCCTCGCAC[C/G]TCAGCCTCCTGAGTA | 27342 |
| rs750349208 | in-del | -/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766757 | CGAGACAGGGTTTCA[-/C]TCTGTTGCGCAGGCT | 27342 |
| rs750366539 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728092 | CGCTCCTCATCACCC[C/G]CAGCAGCTCAGGGCT | 27342 |
| rs750411217 | snp | C/T | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758766 | CTCTTTTGGTGGTAC[C/T]CTTGCTCTCTTTTTA | 27342 |
| rs750480712 | snp | C/G | | | utr-variant-5-prime, stop-gained | RABGEF1 | GRCh38.p7 | 7:66795533 | GCATTGAAGAACAGT[C/G]AGAGTGTGCTCAGGA | 27342 |
| rs750481695 | snp | A/G | 3.29533e-05 | 0.00405901 | missense | RABGEF1 | GRCh38.p7 | 7:66805173 | CCAAGCGTGTGCCTC[A/G]AGACAAGCTGGCCTG | 27342 |
| rs750486885 | snp | C/G | 1.65187e-05 | 0.00287386 | missense | RABGEF1 | GRCh38.p7 | 7:66799377 | TGTTAATGAAGACAT[C/G]CCAGAAGTGTCTGAT | 27342 |
| rs750496525 | snp | C/T | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681914 | CCACAGACTAGGAAA[C/T]GTTGGTTTCTCCGGG | 27342 |
| rs750498813 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694518 | GGGAAGCCAGCAAAG[A/G]GCATTGAGCTAAAGA | 27342 |
| rs750530809 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797167 | AAATTATTCAGGCAT[A/G]GTGGCGTGTGCCTGT | 27342 |
| rs750539184 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773029 | AGAATTCTAAAACTG[C/T]TTCAACAGAAGAAAG | 27342 |
| rs750559076 | in-del | -/AACA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733698 | GTGAGGCTCCATCTC[-/AACA]AAACAAAACAAAACA | 27342 |
| rs750589473 | snp | G/T | 0.00172861 | 0.0293482 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773909 | GAGCTCAAGTGATCC[G/T]GCCGCCTTGGCCTCC | 27342 |
| rs750663503 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751176 | GCTGGAATTACAGAC[A/G]TGCGCCACCGCACCT | 27342 |
| rs750701310 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704375 | TGCTTTAATGGACTG[A/G]TGGATTTCTGGAGGT | 27342 |
| rs750718237 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763782 | CTTAGCATGTTTTCA[A/G]GGTTCACCATGTTGT | 27342 |
| rs750722010 | snp | C/G | 1.74348e-05 | 0.00295247 | intron-variant, missense | RABGEF1 | GRCh38.p7 | 7:66783812 | TATAAACAGACCAAG[C/G]TGTTTTTGGAAGGAA | 27342 |
| rs750730172 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783336 | TTATAAACTCCAGCA[A/G]TCTTTGAGAAGCCTA | 27342 |
| rs750758805 | snp | C/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754755 | TTCACGTCTAGGCAT[C/T]GCGTTTTGTATTTCT | 27342 |
| rs750795423 | in-del | -/ATT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720172 | CAACATCCATTCATT[-/ATT]ATTATTATTATTATT | 27342 |
| rs750799321 | snp | C/G | | | intron-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758518 | GGAGCGATGTGTGGC[C/G]CCTCGGAGCTCCCTC | 27342 |
| rs750816050 | snp | G/T | | | intron-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811712 | ATCAATATAGAGCTA[G/T]TATTGTCTGTTGGTG | 27342 |
| rs750830713 | in-del | -/TACTAA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686114 | GCGAAACCCCGTCTC[-/TACTAA]AATACAGAAAACTTA | 27342 |
| rs750851811 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798031 | CTAAGGCACGAGAAT[A/G]GCTTGAATCCAGGTG | 27342 |
| rs750877015 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684045 | CCGAGCCTGGAGGGT[G/T]GTTATTAAAGAGAAA | 27342 |
| rs750886789 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772898 | GCTTGGGAGACAGAG[C/T]GAGACTCTGTCTCAA | 27342 |
| rs750911568 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742179 | AGAGTCTGTTCCTTA[A/C]AATTGTTGTACCAAG | 27342 |
| rs750968847 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785675 | GTCAGGAGATAGAGA[C/T]CATCCTGGCTATCAC | 27342 |
| rs750978828 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714976 | GAAATTTAGGTTATC[A/G]ATTAGAAAACTTTCG | 27342 |
| rs751031531 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699654 | CTGGGATCGTGCCAC[C/T]GCACTCCAACCTTGG | 27342 |
| rs751050225 | snp | A/G | 1.65375e-05 | 0.0028755 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66771978 | GGATGTGGTTACTAC[A/G]GCAACCCTGCCTGGC | 27342 |
| rs751067947 | in-del | -/TCTTTT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744040 | TCTTTTCTTTTCTTT[-/TCTTTT]TTTTTTTTTTAAGAC | 27342 |
| rs751104991 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781752 | TAGTGTTTGCATGAT[A/G]TTTTGCCATGCAAAT | 27342 |
| rs751129673 | snp | A/G | 3.30841e-05 | 0.00406706 | missense | RABGEF1 | GRCh38.p7 | 7:66808904 | TGTGCTGTGGCTTTC[A/G]TTGAGAAGCTAGACG | 27342 |
| rs751175425 | snp | C/T | 1.66902e-05 | 0.00288874 | intron-variant, missense | RABGEF1 | GRCh38.p7 | 7:66783693 | TTCAGGAAGCAAAAG[C/T]TCCCAGTCCTTCCAT | 27342 |
| rs751191992 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711584 | TCTATTTGTATACTC[C/T]ATTCTTTTCTTTTTT | 27342 |
| rs751207256 | snp | A/G | 1.64855e-05 | 0.00287097 | missense | RABGEF1 | GRCh38.p7 | 7:66809019 | GGTCTCCTGATGCTT[A/G]CTTAGGCGTCAAGCA | 27342 |
| rs751208842 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769970 | CCAAGACCCTTTCAA[C/T]ACAAGGCTCTTTAAG | 27342 |
| rs751271127 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698394 | TCATCAAAGTGGGCA[G/T]CCCACGAAAGAGAGT | 27342 |
| rs751330860 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714324 | GAAATTGGTTCATTT[A/C]ATCTACATTGTTAAA | 27342 |
| rs751336446 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804533 | TGAGGTCAAGAGTTC[A/G]AGACCAGCCTGGCCA | 27342 |
| rs751381978 | snp | C/T | 1.72365e-05 | 0.00293563 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797360 | TTGATCTTTTCTCTG[C/T]CTGGTTATTTCAGTG | 27342 |
| rs751392276 | in-del | -/TTC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699258 | GGCACGGGGCATACA[-/TTC]TTCTTTTTCTGCCTC | 27342 |
| rs751443374 | in-del | -/TTTG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744877 | TGATTTCTTTGATTT[-/TTTG]TTGCTGGTTTTCAGT | 27342 |
| rs751459477 | snp | A/C | 1.82261e-05 | 0.00301872 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771861 | ATAATTCATTTTCAA[A/C]AGCACTTTCTTGTTT | 27342 |
| rs751465403 | snp | C/G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693049 | AAAAAAGCAGTGAGC[C/G/T]GGCTGGTCCCGTGGC | 27342 |
| rs751610619 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719325 | TACCATCTTAGCCTC[C/T]TGAGTAGTTGGGAAC | 27342 |
| rs751648730 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810954 | TTCACTGAGTCAGCT[C/G]GTTCCCAAGCTCGCA | 27342 |
| rs751656418 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684403 | AACCGAGGTTGCACC[A/G]GTGCACTCCAGCCTG | 27342 |
| rs751657929 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734979 | GAACATTTATAAAAC[C/T]CCTTAGGAAGTTTCA | 27342 |
| rs751676889 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713994 | GAGTTTTTTTGGTCT[A/G]TGTTCATAGAGACTA | 27342 |
| rs751685722 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811146 | CAGTTCGTTTAGTTA[C/T]TGTACACTCTGTTTG | 27342 |
| rs751709633 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751496 | GGTCTGGATGATGCT[A/G]TTTTTCAGAGAAGAA | 27342 |
| rs751712145 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724628 | CTCCCAAAGTGCTGG[A/G]ATTATAGGCGTGAGC | 27342 |
| rs751726342 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66753310 | GTGTATGATTGTCCT[A/G]TTTGTAAAGAACAGG | 27342 |
| rs751740897 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733340 | CACCAATGTGACACT[A/G]GTGTGACATTGACTG | 27342 |
| rs751775810 | snp | C/G | 4.962e-05 | 0.00498072 | missense | RABGEF1 | GRCh38.p7 | 7:66809213 | AATCAACCGTTAGCA[C/G]CTATTGACTCTGAAA | 27342 |
| rs751806301 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731384 | GAAGGCACCGTGTGG[G/T]GTTGAGGCTCTAAGA | 27342 |
| rs751826935 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686044 | AACACTTTGGGAAGC[C/T]GAGGTGGGCAGATCA | 27342 |
| rs751875694 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766607 | TTGAGAGTTTTTTCT[A/G]ATTAGATTTCCCTCT | 27342 |
| rs751877444 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726486 | CCTCCCACCTCAGCC[C/T]CCAAGTAGCTGAGAC | 27342 |
| rs751903487 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786664 | CCAACTTGGCCTCCC[A/G]AAGAGCTGGGATTAT | 27342 |
| rs751911654 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773338 | AGCTTCCTCCCCTCA[C/G]CACATAAAAATGTCC | 27342 |
| rs751925632 | in-del | -/T | 0.0137625 | 0.0818036 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796897 | CACCCAGCTGGTAAG[-/T]TTTTTTTTTTAAGCG | 27342 |
| rs751925810 | snp | A/G | 1.65395e-05 | 0.00287567 | missense | RABGEF1 | GRCh38.p7 | 7:66799391 | TCCCAGAAGTGTCTG[A/G]TATGGTGGTGAAGGC | 27342 |
| rs751944318 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720598 | TAAAGCTAATATTTT[A/G]ATGGATAAAGTATGA | 27342 |
| rs751958513 | snp | A/T | | | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740159 | ATTTCTTTTGTAGAG[A/T]TGGTGACCTTGCTCT | 27342 |
| rs751972483 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715097 | TCTCCTCCTTCTCCT[C/T]TCCTCCTCCTCCAAC | 27342 |
| rs751992842 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718000 | TTTTTTGTATCTTCT[A/G]TTTTCCTGCTGAGGG | 27342 |
| rs752025321 | in-del | -/GCTTT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695442 | CCGTCATGGGCAGGG[-/GCTTT]GACGCAAGAGGTTCC | 27342 |
| rs752056249 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702279 | TGTATGGATAGACCA[C/T]AATTTGTTTATCCAT | 27342 |
| rs752057476 | in-del | -/TG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797300 | CAGAGCCAGACTCTT[-/TG]TTTGCAAAAAAAAAA | 27342 |
| rs752074196 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700980 | AGTGTGGTGGGCAGC[A/G]CTGTCTTGCAGCCCA | 27342 |
| rs752085622 | in-del | -/AT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746113 | TTACAATATGTAAAC[-/AT]GTGAAATAACAGTTA | 27342 |
| rs752125163 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806519 | TGCTCTTGATCAGAA[C/T]GATGCTTTTACCTTT | 27342 |
| rs752141600 | in-del | -/AGTGA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773120 | AGCCAATATTTGTTG[-/AGTGA]CTCCTTTGCTGTCAT | 27342 |
| rs752204090 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690747 | AAAATTAAATTTACA[A/G]AAAGAGAAAACACTG | 27342 |
| rs752207331 | snp | C/T | | | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760532 | CATCACAACCTCTTC[C/T]TCCCGGGTTCAAGTG | 27342 |
| rs752220565 | snp | C/T | | | utr-variant-5-prime | RABGEF1 | GRCh38.p7 | 7:66740759 | GGCGAAGCGGGCGAG[C/T]GGTGGTTTGGACGCC | 27342 |
| rs752228202 | in-del | -/T | 1.64762e-05 | 0.00287016 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795617 | TTAGCCATTGAGAGA[-/T]TGCGGGTATTGCACA | 27342 |
| rs752249918 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771341 | AGACAGGGTTTCACC[A/G]TGTTAGCCAGGATAC | 27342 |
| rs752255174 | in-del | -/TT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687115 | CCACCACGCCCGGCT[-/TT]TTTTTTTTTTTTTTT | 27342 |
| rs752262917 | snp | C/T | 1.64817e-05 | 0.00287064 | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66809122 | ACTGGAAAAAGACCT[C/T]ATAGATTGGACAGAT | 27342 |
| rs752265977 | snp | A/G | 7.35984e-05 | 0.00606579 | intron-variant, missense | RABGEF1 | GRCh38.p7 | 7:66783831 | TTTTGGAAGGAATGC[A/G]TTACAAAAGGGTAGG | 27342 |
| rs752312057 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785163 | TAGACTTCTAAATGA[A/G]TATACTAAAGTAAAG | 27342 |
| rs752319609 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804791 | GTAGACATGGTTTCA[A/G]ATTCCCACCCTGCTA | 27342 |
| rs752350198 | snp | C/T | | | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760677 | TCAAACTCCTGACCA[C/T]GTGATCTGCCCGTCT | 27342 |
| rs752350853 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699513 | CTGGCCAACGTGGTG[A/T]AACCCCGTCTCTACT | 27342 |
| rs752373829 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742040 | CCTGTAGTCCCAGCT[A/G]CTCTGGAGGCTGAGG | 27342 |
| rs752377570 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729201 | AGGATCCACCCACCT[C/T]GGCCTCCCAAAGTGC | 27342 |
| rs752407480 | snp | C/G | 3.57385e-05 | 0.00422705 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771880 | ACTTTCTTGTTTGTT[C/G]AGTGGTTAGCAGGAA | 27342 |
| rs752419769 | in-del | -/AG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784276 | AGTTAGAGAAAGGAC[-/AG]ATAGAATTTAGACAA | 27342 |
| rs752456282 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688592 | TCATGGAATGAAACT[A/G]GACATCAGTAACCAG | 27342 |
| rs752478094 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793526 | TCTGTAGTAATAATC[A/C]CAAGAATGAATATAG | 27342 |
| rs752498033 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695111 | GAGATCAGAAGGTCA[A/G]GACCAGCCTGGCCAA | 27342 |
| rs752502197 | snp | C/T | 3.31785e-05 | 0.00407286 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797545 | TTGTAGTTACTACCT[C/T]CTAATGGAAGAACAC | 27342 |
| rs752528232 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766828 | CTCCCAGGTCCAAGC[A/G]ATTCTTGTGCCTCAG | 27342 |
| rs752542164 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695880 | CTGACGCAGGAGTAT[C/G]ACTTACATCTGGGAG | 27342 |
| rs752591160 | in-del | -/ACAAATACAAAATAC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778276 | TGCCATACGTAGCAG[-/ACAAATACAAAATAC]CTTGGTAGCAGACAA | 27342 |
| rs752600117 | snp | A/G | 1.65891e-05 | 0.00287998 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66772010 | GGGTTTCTGCTCCAA[A/G]TGCTGGAGGGAAGAG | 27342 |
| rs752676135 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729051 | TGCCTCCTGGGTTCA[A/G]CCGATTCTCCTGCCT | 27342 |
| rs752720405 | snp | A/G | | | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756179 | CAAAGAAAATATACT[A/G]GTGCTAATAAATATC | 27342 |
| rs752736325 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708793 | CTCTAGCCTGGGTGA[C/G]AGAGCAAGACCCTGT | 27342 |
| rs752741594 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735030 | GAAAATTTATGAATG[C/G]TTTTCCAGAGGCTAA | 27342 |
| rs752756002 | snp | A/C/T | 7.14827e-05 | 0.00597804 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783642 | ATGGATCTTTTATGT[A/C/T]ATGAAACTTACTATG | 27342 |
| rs752805993 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800555 | CTTTTCTGCTAGGCT[A/G]TGGCGTAGGTCATGA | 27342 |
| rs752810461 | snp | C/T | 1.67823e-05 | 0.0028967 | missense | RABGEF1 | GRCh38.p7 | 7:66797374 | GTCTGGTTATTTCAG[C/T]GCCTCCAGAAAGAGT | 27342 |
| rs752816531 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684698 | GGAGTGCAGTGGCCT[A/G]ATCTTGGCTCACTGC | 27342 |
| rs752825207 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767767 | CCACCAGACACCAAC[A/G]TCTGTTGACTTCCTG | 27342 |
| rs752856189 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774612 | CCTATTCAGCCTTAT[C/T]AGTCAGGTGTGGTGG | 27342 |
| rs752873298 | in-del | -/CT | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755285 | GGCAACAGAGTGAGA[-/CT]CTGTCTCAAAAAAAA | 27342 |
| rs752874008 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733566 | AGCTGGGCATTGCAG[C/T]GCATTCCTGTAATCC | 27342 |
| rs752891142 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714065 | AGTTTTGATGTAAAG[A/G]TAATGTTGGCTTTAT | 27342 |
| rs752891350 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727277 | GATTTGCCAGTGGAG[C/G]TGGCCCTGGTTCTTG | 27342 |
| rs752894047 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765344 | TATTGTTATTGTTTC[C/T]GTCTAATACATAGTG | 27342 |
| rs752932803 | in-del | -/CAA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687483 | TTCTGTTGTTTAAGC[-/CAA]AAAAAAAAAAAAAAG | 27342 |
| rs752935034 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721567 | ACTTATCTCTGCTTC[C/T]ATTATCACATCTCTT | 27342 |
| rs752948223 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792692 | TGCCTTTGCTCACAG[A/C]TAGGTAGAAAGAGAT | 27342 |
| rs752984980 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741922 | AGGCGGATCATGACG[-/T]TCAGGAGCTTGAGAC | 27342 |
| rs752999891 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801697 | TGTTTCATCCATGTT[A/G]TTGCAAATGACTGGA | 27342 |
| rs753019247 | snp | C/T | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758051 | TGAGGTCAAAGGATA[C/T]CTTATCGTTTTACTA | 27342 |
| rs753023162 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710000 | ATATTTTATTTTGCT[G/T]TCATTTTTAATTTTA | 27342 |
| rs753052671 | snp | C/T | 3.29473e-05 | 0.00405864 | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66805213 | GTGCAGCAAGCACAT[C/T]TTCAATGCCATCAAG | 27342 |
| rs753069780 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799823 | AAGGCAAGGTAATCC[C/T]CACGCTGGAGTAACG | 27342 |
| rs753074604 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797797 | TTCTTGGTCCATTAC[C/T]ATCTCCTCAAGTGGG | 27342 |
| rs753077071 | snp | A/G | 0.000115307 | 0.00759211 | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66805336 | TATCCAGTATATCAC[A/G]CGCTTCTGCAATCCA | 27342 |
| rs753100736 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703605 | TCGGAAATCAGTTGA[C/G]AATAGATGTATTGGC | 27342 |
| rs753110343 | snp | A/G | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680747 | AGGTCAGGAGTACTA[A/G]ACTAGACTGGCCAAT | 27342 |
| rs753160883 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763556 | ATACCATAGAATTCT[C/T]CCTTTTGAAGTGCAC | 27342 |
| rs753166917 | snp | C/T | 1.65162e-05 | 0.00287365 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66775372 | TTCTTCAGTGCATCT[C/T]CCAGGGTCGGATCAA | 27342 |
| rs753190723 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693088 | AGCTGAAAGGCACGT[C/T]GTTCTAGAAGCCCTG | 27342 |
| rs753198057 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774855 | CCCAGCAGATTGAGT[G/T]GTTCTTTCCTGTGTT | 27342 |
| rs753205577 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692149 | GTTACATTTCTAGCA[C/T]TCGGTAGCTCTACCG | 27342 |
| rs753252688 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762985 | AAGGATAGCAGTTTA[A/C]AACACTCATTTATTT | 27342 |
| rs753253950 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806038 | GCATGAGCCACCACT[C/G]CTGACCTGAATTCTT | 27342 |
| rs753260239 | snp | A/G | 1.64735e-05 | 0.00286993 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66795516 | TCTGTTTCAGGATCT[A/G]AGCATTGAAGAACAG | 27342 |
| rs753260445 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698986 | AGCAACAAAGCTGAG[A/T]CCAGCCCGTCCTTCA | 27342 |
| rs753270867 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808808 | TTTTAAATGGTCTGT[C/G]ATCAAAAGATTTTTA | 27342 |
| rs753282089 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795737 | CTGGGAACTGGTCTT[A/T]TACTTAGCAGTGCCT | 27342 |
| rs753289967 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776881 | AATAGCCAGGTAGTA[A/C]GGTGACTTTGGAGTC | 27342 |
| rs753303196 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708921 | GGGATAGGGAAAAAA[A/C]GAAATATGCAATATG | 27342 |
| rs753422944 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779193 | CAAAAATCATAATCC[A/G]TGTGTTAATTTAGTA | 27342 |
| rs753448538 | snp | A/G/T | 4.94298e-05 | 0.0049712 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795625 | TGAGAGATTGCGGGT[A/G/T]TTGCACAGGGATGAC | 27342 |
| rs753454222 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793890 | GTGTGAGGTCAGTGG[A/C]CTGTGTAGATGAAGT | 27342 |
| rs753456709 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804988 | CCATGAGTATGAGAT[C/G]ATATTTACTAAGTTA | 27342 |
| rs753461069 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795140 | GAGCCCAGGATTCTA[C/G]CTGCTGGCAGGAAGC | 27342 |
| rs753464848 | in-del | -/TTGT | | | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757280 | CTTTCTAACTTGTTA[-/TTGT]TTGTTTCTCTGTTAC | 27342 |
| rs753467821 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731209 | CCAGGCCTGGCAACA[C/G]GACTTGGCAGAATGT | 27342 |
| rs753474851 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691817 | CCAACACTTTGGGAG[A/T]CTGAGGCGGGAGGAT | 27342 |
| rs753486829 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761619 | CCTGACACCAGCATT[C/T]GTCCCTCAGAGTACA | 27342 |
| rs753502038 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749964 | GGGCGACAGAGCGAG[A/T]CTCCATCTCAAAAAC | 27342 |
| rs753548714 | in-del | -/TGTG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702348 | GGCTATTGTTTTGTT[-/TGTG]TGTGTGTGTGTGTGT | 27342 |
| rs753556265 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720396 | AGAGACGGGGTTTCG[A/C]CATGTTGGCCAGGCT | 27342 |
| rs753598090 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748611 | AGAATAAAATCATAA[C/G]GGCTAGTTCAAGGGT | 27342 |
| rs753609598 | in-del | -/AT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796322 | GGATATACTTAGCAC[-/AT]GTGTGTGTCAGAGAA | 27342 |
| rs753609687 | in-del | -/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738642 | GAGGTGGAGGCAGAA[-/G]GATCACTTGAGCCAG | 27342 |
| rs753617912 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780092 | GAAAAGTATGTGTGG[A/G]AGGGAGGCATGTTGT | 27342 |
| rs753617985 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767203 | AGACGAGGTTTTGCC[A/G]TGTTGGCCAGGCTGG | 27342 |
| rs753655402 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715513 | TGACATGTTCTATTT[G/T]CATTTTCATTCAAAT | 27342 |
| rs753671840 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731223 | AGGACTTGGCAGAAT[A/G]TCCTTGAGGAGTTCA | 27342 |
| rs753672624 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758166 | AATAGGAAGCGGACC[A/G]CCAAGAAGGATAGAG | 27342 |
| rs753679025 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66685733 | AAAATGTTACCAGTA[A/C]TTACTCATTGTGATG | 27342 |
| rs753756481 | in-del | -/TGTTTA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783103 | TTGTATGCTTTGTTG[-/TGTTTA]TCATGCTATTAATAC | 27342 |
| rs753771798 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709870 | TACACCTAGGAGGTA[A/G]TACTAGAAACAATTG | 27342 |
| rs753774917 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785747 | GGCGTGGTGGCAGGC[A/G]CCTGTAGTCCCAGCT | 27342 |
| rs753775194 | in-del | -/T | 3.35962e-05 | 0.00409841 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775410 | AATGTTCTGATACTC[-/T]TTTTTTTTCTTCTCT | 27342 |
| rs753841111 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793976 | TGACATCCTTATGAG[A/G]ACCGTTGGGAGAAAT | 27342 |
| rs753861242 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762846 | TGAAGGCCTCTCACA[C/G]TCTGATGTGAAAGCT | 27342 |
| rs753864723 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696956 | CATGGGGGATGGGGA[A/G]CAAGATACATGGGAG | 27342 |
| rs753894307 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736957 | ACACGTACACACACA[C/T]GCACACAAATATATA | 27342 |
| rs753921396 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704974 | CCAATTTGCATTCCC[A/G]CCAGCAATAGATGAG | 27342 |
| rs753953020 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693148 | GCACAGTGACAGGGT[A/G]TAAGGGGGAGATTCG | 27342 |
| rs753963734 | snp | A/G | 3.36712e-05 | 0.00410298 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66772040 | GTACCACAAAGCCAG[A/G]CAGAAGCAGATTCAG | 27342 |
| rs754001281 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732926 | GCTCGCCCTGCTTCT[C/T]TAAACTTCTCGGCAG | 27342 |
| rs754013703 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737172 | TGGCTTTAGGCAATC[C/T]TCCCACCTTGACCTC | 27342 |
| rs754019517 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693135 | GACAGAGCATTTGGC[A/G]CAGTGACAGGGTGTA | 27342 |
| rs754041300 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763161 | AGCCATTGCCCCTAG[G/T]CCACAGCACTCATTT | 27342 |
| rs754077025 | snp | G/T | 1.65179e-05 | 0.00287379 | missense | RABGEF1 | GRCh38.p7 | 7:66799372 | GTCCCTGTTAATGAA[G/T]ACATCCCAGAAGTGT | 27342 |
| rs754099769 | in-del | -/TA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714628 | TGATTTTACTCTTTT[-/TA]TAGTTTCTTAAAACA | 27342 |
| rs754121727 | snp | A/G | 1.68721e-05 | 0.00290444 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808871 | TATGACTGTATTAAC[A/G]TCCTCTTCTTGTAGT | 27342 |
| rs754129281 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775671 | CCCATCCAAATGACT[A/C]TCTCTTTGGATGTTT | 27342 |
| rs754150367 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763702 | TGTCTCTAGATTTCC[C/G]TGGTATGGATGTTCA | 27342 |
| rs754161440 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699199 | GGCTAGAGCCCCTCT[C/T]CAGGGAGAGCTAGGG | 27342 |
| rs754167821 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802923 | AAAAATAAAGATTAA[C/T]AAGAAAGTAGTTTAA | 27342 |
| rs754182124 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810597 | TTGACAGCTACCTGC[A/G]TTGTAGAACCTTTTC | 27342 |
| rs754215665 | snp | C/T | 1.77995e-05 | 0.00298319 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783644 | GGATCTTTTATGTCA[C/T]GAAACTTACTATGTT | 27342 |
| rs754306775 | snp | C/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739513 | ACAAAAAAAAAAATA[C/T]GAGCTGGGCGTGGTG | 27342 |
| rs754306813 | snp | G/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754626 | AGTCCAGCTCAGCTG[G/T]ATGTCATTTACATAT | 27342 |
| rs754313386 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783279 | TAAGTCATTTAACAT[G/T]TCAGTGCTTCTATTG | 27342 |
| rs754325492 | snp | A/C | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680856 | GAAGGCCAAGGCGGG[A/C]GGATCACTTGAGGTC | 27342 |
| rs754334374 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782012 | TTCCAGTTGTTAAGA[G/T]AGTAGAGTAAACCTG | 27342 |
| rs754394558 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66753451 | TGCTGTAAAATATTA[C/T]AGGCATACTTTGGAG | 27342 |
| rs754394922 | snp | A/G | | | intron-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758348 | AGAATAAAACCTAGC[A/G]CCGAGGCACAATTTA | 27342 |
| rs754402981 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797933 | AGTAGCCCAGGCAAC[A/G]TGGTAAAACCCCGTC | 27342 |
| rs754463269 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724321 | AGCAACTTGATTGTG[A/G]TATGTTTTGGTGTGG | 27342 |
| rs754494337 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769976 | CCCTTTCAACACAAG[G/T]CTCTTTAAGGTCTAT | 27342 |
| rs754496301 | snp | C/T | 1.65116e-05 | 0.00287324 | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66808918 | CATTGAGAAGCTAGA[C/T]GCCCAGTCTTTGAAT | 27342 |
| rs754505390 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780022 | GCTAGTAGAGTTAAT[C/T]CTCATTTACATTTTA | 27342 |
| rs754583202 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760276 | GGTTGTAGAAATCCT[A/G]GAGTATGTGACCTTT | 27342 |
| rs754587901 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781761 | CATGATATTTTGCCA[C/T]GCAAATTCTGGTCAC | 27342 |
| rs754590266 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718378 | ATAGTTAAATAGCTG[C/T]TTTAAAATCCTGGTT | 27342 |
| rs754613911 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803338 | TGAAAGAACCCTTTG[G/T]TATACCCCACCGCCT | 27342 |
| rs754619667 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698651 | TCCCTGCAAGGCTGC[A/G]GTGATCCCCTGTGAA | 27342 |
| rs754643606 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807360 | TCTCATAGCACTCTC[C/T]AAGAGTCCTTTGTTC | 27342 |
| rs754661298 | snp | A/T | 0.000118494 | 0.00769631 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797367 | TTTCTCTGTCTGGTT[A/T]TTTCAGTGCCTCCAG | 27342 |
| rs754677345 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776900 | GACTTTGGAGTCACT[A/C]CTGGTTTGAGCCCTA | 27342 |
| rs754679735 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693998 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 27342 |
| rs754690178 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771151 | TAAAAATTTTTTATT[A/T]CTTTTGAGACAGAGT | 27342 |
| rs754703893 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747104 | CGGCCCTAGTGGAAC[A/G]TTTTAATTTGTTTCT | 27342 |
| rs754722431 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703218 | GACCTCGTGCCCGCC[C/T]GCCTTGGCCTCCCAA | 27342 |
| rs754723870 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792633 | CTAAAGCTGTTTTCT[A/G]TAAAGAAATCCTTGA | 27342 |
| rs754726438 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767565 | CTGTCCCCCAAATTC[A/G]TATGTTGAAATTCTA | 27342 |
| rs754743240 | snp | C/T | 1.77209e-05 | 0.0029766 | intron-variant, missense | RABGEF1 | GRCh38.p7 | 7:66783819 | AGACCAAGCTGTTTT[C/T]GGAAGGAATGCATTA | 27342 |
| rs754744827 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746021 | ATTAAATGTACACTT[C/G]TTTCATAGAGCACTG | 27342 |
| rs754771372 | snp | G/T | | | utr-variant-5-prime, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66682106 | GGGCGTGCGCTGGCG[G/T]TGCCGGGGGGGCGGG | 27342 |
| rs754778662 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691849 | ACTTGAGCCCAGGAG[A/G]TCAAGACCAGCCTGA | 27342 |
| rs754791605 | snp | A/G | 5.44786e-05 | 0.00521884 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771863 | AATTCATTTTCAACA[A/G]CACTTTCTTGTTTGT | 27342 |
| rs754796061 | snp | A/T | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759607 | CATTGCAGCTTCTGC[A/T]TCTAGGGTGGCCTCA | 27342 |
| rs754811796 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791667 | AAGGTTTTCAAAACT[A/G]GAAGTGGAAACAAAG | 27342 |
| rs754840194 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694936 | TTCCGGACATGCTGG[C/T]CTGGAGCCCTGTTGA | 27342 |
| rs754868433 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745882 | GGAGAATCGCTTGAG[C/T]CTAGGAGTTCCAGGC | 27342 |
| rs754952427 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799309 | GCTCTTGTTTACTGT[C/G]TCTCTCTCTTTAGAG | 27342 |
| rs754955685 | in-del | -/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692513 | CATCACCATGAAGGA[-/G]CTGAGGGACTGTGTT | 27342 |
| rs754967346 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764178 | TCCTACTGGATGTGA[A/G]GTGGCATCTCATTGT | 27342 |
| rs755058943 | in-del | -/TTT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687114 | GCCACCACGCCCGGC[-/TTT]TTTTTTTTTTTTTTT | 27342 |
| rs755081204 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730307 | CTCACTGTTTCTGCT[C/G]AGCGCCAGCTTCCTC | 27342 |
| rs755113919 | in-del | -/TG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738024 | TTTTGTTTTTTTTGT[-/TG]TTTTTTTTTTTTTTG | 27342 |
| rs755131505 | in-del | -/TTTTTTTTTTTTTTTTTTTTTTT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705877 | ACCACACCCAGCTAA[-/TTTTTTTTTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTG | 27342 |
| rs755139492 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765668 | CCTGATACTCAGACC[A/G]CTTGATAGAAGGATC | 27342 |
| rs755271370 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715718 | GGTTTATTTTGTGAC[C/G]AAGGACATAATCTTA | 27342 |
| rs755271712 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741378 | CTGAGGGCGAGGCTG[C/T]GGGGCCGGGGTTAGG | 27342 |
| rs755274317 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785935 | CAAAACCTTTAAATT[A/G]ATGTTATTACCACCA | 27342 |
| rs755284429 | snp | C/T | 0.00302571 | 0.0387776 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796828 | ACTCCTGACCTCAGG[C/T]GATCCACCTGCCTCA | 27342 |
| rs755291335 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774475 | CTGGAGCCTTCCTGT[A/G]TATCCAGCATCACAG | 27342 |
| rs755295337 | snp | A/G | 1.65474e-05 | 0.00287636 | missense | RABGEF1 | GRCh38.p7 | 7:66799393 | CCAGAAGTGTCTGAT[A/G]TGGTGGTGAAGGCGA | 27342 |
| rs755351164 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721488 | TTCCTTGGCTCATGG[A/C]CTCTTCCTCCATCAT | 27342 |
| rs755387559 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773408 | GAGGGGTCCCGATTC[C/T]ACCCTCAGACTTAGC | 27342 |
| rs755412951 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771437 | AGCCACCACACCGGC[C/T]TGTGCAGACATTTTA | 27342 |
| rs755446377 | in-del | -/AAAAAC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762066 | CTCAAAAAAAAACAA[-/AAAAAC]AAAAACAAAAACATA | 27342 |
| rs755451043 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761772 | AACAAAAGCCTGGGG[G/T]TGGGCGTGGTGTCTC | 27342 |
| rs755468652 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695447 | ATGGGCAGGGGCTTT[A/G]ACGCAAGAGGTTCCA | 27342 |
| rs755504130 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702357 | TTTGTTTGTGTGTGT[G/T]TGTGTGTGTGTGTGT | 27342 |
| rs755526185 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794505 | AAATAGCCTTTAAAT[A/G]TTCTTTGGCAGAAAG | 27342 |
| rs755528469 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690994 | TGCTTCGGAGGCTGG[A/G]GCATGAGAATCGCCG | 27342 |
| rs755579657 | in-del | -/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773145 | TTGCTGTCATTTGTA[-/G]TGAACTCAGAGAATT | 27342 |
| rs755609970 | snp | A/C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719455 | AGCACCTCGGCCCCC[A/C/T]GCAGTGTGCTGGGAT | 27342 |
| rs755614976 | snp | A/T | 1.95996e-05 | 0.0031304 | intron-variant, splice-donor-variant | RABGEF1 | GRCh38.p7 | 7:66783843 | TGCATTACAAAAGGG[A/T]AGGTTGAGAATAACC | 27342 |
| rs755615208 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803514 | CCACGTGCTTCAGCA[A/C]CCTTCGCTGTCCCCC | 27342 |
| rs755652144 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759718 | TATACACGTTTAAAC[A/G]ACCAGATCTCACAAG | 27342 |
| rs755667342 | snp | A/T | | | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740428 | GAGCCAGCGTCGCCC[A/T]CCAGCTGTTGCGCGT | 27342 |
| rs755705009 | snp | A/T | 3.29462e-05 | 0.00405857 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66795512 | TCTCTCTGTTTCAGG[A/T]TCTAAGCATTGAAGA | 27342 |
| rs755731158 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718538 | CATAGTGTTACGTGG[A/T]TAAATTCTATGGAGA | 27342 |
| rs755740126 | in-del | -/AGTA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700535 | TGGGGGAGGGGACTT[-/AGTA]AGAGGGTACAGCTCA | 27342 |
| rs755775117 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730144 | AGCAGCACTTCCTCA[C/T]GTCCACGGAGAGTGC | 27342 |
| rs755795206 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746099 | ATCTGGACTATTGTT[-/A]ACAATATGTAAACAT | 27342 |
| rs755802897 | snp | A/G | 1.67702e-05 | 0.00289566 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66772034 | GGAAGAGTACCACAA[A/G]GCCAGGCAGAAGCAG | 27342 |
| rs755825289 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765972 | TTTAAAAAAACTTAA[G/T]TGATCTATACTTAAA | 27342 |
| rs755844452 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735112 | AAGTTTTAACTTTAT[A/C]ATCTGTCTGGAGGTC | 27342 |
| rs755846526 | snp | C/T | | | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760697 | TCTGCCCGTCTCAGC[C/T]TCCCAAAGTGCTGGG | 27342 |
| rs755863390 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779104 | AACAAAGTGAGACTC[C/G]GTCTTAAAAAATAAA | 27342 |
| rs755866176 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729067 | CCGATTCTCCTGCCT[C/T]AGCCTCCCGAGTAGC | 27342 |
| rs755894170 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748216 | TTTTGTGTAAGACGG[C/T]GACATAACATCAAAA | 27342 |
| rs755910267 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695881 | TGACGCAGGAGTATC[A/G]CTTACATCTGGGAGT | 27342 |
| rs755914353 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806259 | GTACGTGAATCTCTC[A/C]GTCTCTAAAAATATG | 27342 |
| rs755931912 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748533 | ATGGAACAGTCTGAC[A/G]AGGGCACATATTTGT | 27342 |
| rs755933399 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692243 | TGGGCAGTGCTGTTT[A/C]GGAAGGTCCCTTGGG | 27342 |
| rs755951345 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778045 | TTTCACAGATCACTT[A/T]ATATAACTTAGCCAG | 27342 |
| rs755957583 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714229 | GTTTTTTAACAACAA[A/G]TTCAATTTCGTTAAT | 27342 |
| rs755957758 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727282 | GCCAGTGGAGCTGGC[C/G]CTGGTTCTTGTCCGT | 27342 |
| rs755970741 | snp | A/G | 6.5925e-05 | 0.00574092 | missense | RABGEF1 | GRCh38.p7 | 7:66808941 | CTTTGAATCTAAGTC[A/G]GGAGGATTTTGATCG | 27342 |
| rs755997680 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708811 | AGCAAGACCCTGTCT[C/T]GAAAAAAAATTTACA | 27342 |
| rs756071270 | snp | G/T | 1.72314e-05 | 0.0029352 | missense | RABGEF1 | GRCh38.p7 | 7:66809276 | CAACCTCAAGTTTAT[G/T]CAGGATGATCACAAT | 27342 |
| rs756089840 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766908 | CACTGTGTTACCTCA[A/C]GTCCTCTAATTGTAG | 27342 |
| rs756113640 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695164 | TAAAAAGACAAAGAT[A/G]AGCCGGGCACGGTGG | 27342 |
| rs756155453 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710537 | CATTTTATATCTTTG[G/T]CAGCACTTATATGAT | 27342 |
| rs756241372 | in-del | -/AT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691511 | TTGGACCCAAAAAAC[-/AT]ATACACATGGTCTGT | 27342 |
| rs756254290 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733676 | GCACTCCAGACTGGG[A/C]TACAGAGTGAGGCTC | 27342 |
| rs756261015 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785967 | CTAAACTTTCTAGAT[G/T]GTATCCTAAGGGCCT | 27342 |
| rs756270950 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734914 | CACAAAACTGCTCAC[C/T]ACATGGCCAAACAGG | 27342 |
| rs756312293 | in-del | -/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712778 | GCACCCAGCCTCTTT[-/C]TGAAGATTTCTTGAG | 27342 |
| rs756325803 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732255 | TAGCCATGGGGCTGA[A/G]CAGGCAGCTGGCGTC | 27342 |
| rs756329564 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715439 | CCCGCCTCTTCTTTT[C/T]TAATATAATCATTTC | 27342 |
| rs756332872 | snp | C/T | 1.67539e-05 | 0.00289425 | missense | RABGEF1 | GRCh38.p7 | 7:66797376 | CTGGTTATTTCAGTG[C/T]CTCCAGAAAGAGTCG | 27342 |
| rs756376231 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808810 | TTAAATGGTCTGTGA[C/T]CAAAAGATTTTTACA | 27342 |
| rs756398178 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765592 | GAAATCATTCAGGAC[A/G]TACAGGACCTTCTAC | 27342 |
| rs756399302 | snp | C/T | 1.65378e-05 | 0.00287552 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66775298 | AATCCCTCACATTCT[C/T]CAAGTTTGAAGAAAA | 27342 |
| rs756428857 | snp | A/G | 1.78395e-05 | 0.00298654 | splice-acceptor-variant | RABGEF1 | GRCh38.p7 | 7:66771881 | CTTTCTTGTTTGTTC[A/G]GTGGTTAGCAGGAAG | 27342 |
| rs756435865 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750872 | TTGGAGAAGAATCTG[A/G]GTACTAGAAAATACT | 27342 |
| rs756436887 | snp | A/G | 1.64732e-05 | 0.0028699 | missense | RABGEF1 | GRCh38.p7 | 7:66805338 | TCCAGTATATCACGC[A/G]CTTCTGCAATCCAAG | 27342 |
| rs756438192 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762988 | GATAGCAGTTTAAAA[C/T]ACTCATTTATTTTTT | 27342 |
| rs756475177 | snp | A/G | 1.66112e-05 | 0.00288189 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797551 | TTACTACCTTCTAAT[A/G]GAAGAACACACTGGG | 27342 |
| rs756481321 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773397 | TCCCAGAGAAAGAGG[G/T]GTCCCGATTCCACCC | 27342 |
| rs756483311 | snp | A/C | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680770 | TGGCCAATATGATGA[A/C]ACCCTGTCTCTAGTA | 27342 |
| rs756484345 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711585 | CTATTTGTATACTCT[A/G]TTCTTTTCTTTTTTT | 27342 |
| rs756497032 | snp | C/T | 6.61332e-05 | 0.00574998 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66775380 | TGCATCTTCCAGGGT[C/T]GGATCAAAGAAGGGT | 27342 |
| rs756507115 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737551 | GTGGTTACCAGACTT[C/T]TTTCAGTAGTTTAAA | 27342 |
| rs756519638 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697424 | TCTGTGTTGCCACCA[A/G]GGATGGGTCAAACCG | 27342 |
| rs756535221 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808172 | CTGTTGTTGTTAAGT[A/G]AAAGAGGTGACAGTG | 27342 |
| rs756548072 | in-del | -/ACA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714081 | TAATGTTGGCTTTAT[-/ACA]ACAATTTTGGAAGTG | 27342 |
| rs756571410 | in-del | -/AGCCAAGGTGGGAGGCTCACTTG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751959 | CCCAGCACTTTGGGA[-/AGCCAAGGTGGGAGGCTCACTTG]AGCCCAGGACTTCAA | 27342 |
| rs756578522 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796410 | TGAAAGGATAAGTTT[C/T]ATCAGCATTCATCAG | 27342 |
| rs756583259 | in-del | -/AA | 0.000157583 | 0.00887505 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797329 | AAAAAAAAGAGAGAG[-/AA]AAAATATATATATCT | 27342 |
| rs756634015 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752111 | GGCTGAGGCTCAAGA[C/T]TGCTTGAGGCCAGAC | 27342 |
| rs756681575 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780759 | TTGCTGTGACTTCTC[A/G]AAGAATGAACCTCTT | 27342 |
| rs756698105 | snp | A/G | 1.66015e-05 | 0.00288105 | missense | RABGEF1 | GRCh38.p7 | 7:66809231 | ATTGACTCTGAAAAC[A/G]TTGAAAATGATAAAC | 27342 |
| rs756780071 | snp | C/T | | | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760848 | TGCCCAGGCTGGTCT[C/T]GAACGCTTGACTTTG | 27342 |
| rs756781158 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742527 | GTCTTGAAGAATGAC[-/T]TAACATTCAGACTAA | 27342 |
| rs756797998 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748679 | CTACACAGTAAGAAT[G/T]TCCTTTTCCATTGCA | 27342 |
| rs756808967 | in-del | -/GC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723725 | AGCTGGGATTACAGG[-/GC]TGTGACACCACGCCT | 27342 |
| rs756857465 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806053 | CCTGACCTGAATTCT[G/T]CCTTTTTCTTCCTAC | 27342 |
| rs756904313 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736094 | AATGAAAGGGATGAT[A/G]ATGGAAAAAAACAAG | 27342 |
| rs756912991 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775455 | CAGAGGAGATCCCCA[A/G]TGCTCATAAGCTCAG | 27342 |
| rs756930873 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66706325 | CTTTCATTTCTCTTA[-/T]GCGATACCTAGGAAT | 27342 |
| rs756994427 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749994 | CAAACAAACAAAACT[A/G]CAGAATAATGAAATA | 27342 |
| rs756994485 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735271 | AATCGCTCCTTTGTA[G/T]CCTATTCCAACCGTG | 27342 |
| rs757043573 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66685784 | TCTGTTTACCTATGT[C/T]AGTCTCTGGCTAGAG | 27342 |
| rs757049564 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783197 | AATTGTGAGTCTCCA[C/T]ATAAACACATTAACC | 27342 |
| rs757052956 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780195 | GAGTTGGTGTTCTTC[C/T]GAAGAGTCTTCAGTC | 27342 |
| rs757089562 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702935 | GTAGGGTTTATTTTC[A/G]CTTTTTTGATAGTGT | 27342 |
| rs757131816 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696995 | GTGCAGCCAATGTGC[A/G]TGGAGCAGAGAGAGG | 27342 |
| rs757145065 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785793 | GCAGGAGAATGGCGT[A/G]AACCTGGGAGGCGGA | 27342 |
| rs757154591 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727493 | GCCCTGCCTGGTCAG[A/T]TGGTCTGGACCCCCA | 27342 |
| rs757157102 | in-del | -/GC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737097 | AGAGCGAGAGCGAGA[-/GC]GAGAGAGAGAGAGAG | 27342 |
| rs757167396 | snp | C/T | 3.2969e-05 | 0.00405998 | missense | RABGEF1 | GRCh38.p7 | 7:66809142 | ATTGGACAGATGGAA[C/T]TGCAAGAGAAGTTCA | 27342 |
| rs757175012 | in-del | -/AC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736944 | TATACAGACACACAC[-/AC]GTACACACACACGCA | 27342 |
| rs757203134 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801826 | GACTTCTGTGTGGCT[A/G]TGGGGGCAGTGGTTC | 27342 |
| rs757203988 | snp | G/T | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758177 | GACCGCCAAGAAGGA[G/T]AGAGGGAAACTACTC | 27342 |
| rs757243388 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684859 | CCAGGATGGTCTCGA[C/T]CTCCTGACCTCGTGG | 27342 |
| rs757255751 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787622 | TGTGCCGGGATTACA[G/T]GATTGAGCCACAATA | 27342 |
| rs757288814 | snp | C/T | 6.58913e-05 | 0.00573945 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66795538 | GAAGAACAGTCAGAG[C/T]GTGCTCAGGATTTCT | 27342 |
| rs757342847 | snp | A/T | 5.45896e-05 | 0.00522416 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799280 | AAGACAAATGGCCAC[A/T]GTTTATCCTTGGAGC | 27342 |
| rs757343467 | in-del | -/TGT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730426 | GATAGAGTCTTGCTC[-/TGT]TGTTGCCCAGGCTAG | 27342 |
| rs757363571 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775683 | ACTATCTCTTTGGAT[A/G]TTTTGGTTTTTGTGC | 27342 |
| rs757388079 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737424 | ACACCTGGCTATCCT[A/G]CGCAATACGAGACTG | 27342 |
| rs757427288 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763170 | CCCTAGTCCACAGCA[C/T]TCATTTATTATCTGA | 27342 |
| rs757432863 | snp | A/G | 1.72656e-05 | 0.00293812 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66772070 | GGAGGACTGGGAGCT[A/G]GCGGAGCGGTAAAAG | 27342 |
| rs757433944 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693162 | TGTAAGGGGGAGATT[C/T]GGGGACAGGGTATTT | 27342 |
| rs757453127 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789498 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 27342 |
| rs757460921 | snp | A/G | 3.30153e-05 | 0.00406283 | missense | RABGEF1 | GRCh38.p7 | 7:66808919 | ATTGAGAAGCTAGAC[A/G]CCCAGTCTTTGAATC | 27342 |
| rs757469742 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722892 | TTATTGGCATTTTAA[A/C]AATATTAAGTCTTCC | 27342 |
| rs757473359 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698785 | ACCCAGGGCTCCAGC[-/T]TTTGTGTCAGACCCA | 27342 |
| rs757515908 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746145 | TCCCACTTAATATTA[C/T]TTAACTTATGTTTAT | 27342 |
| rs757520570 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732356 | AGGCCTGGCATCTGG[A/G]CTTGGCTCCCCTGCT | 27342 |
| rs757559852 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776498 | AGGAGTTTGAGACCA[A/G]TCTGGGCAACATGGT | 27342 |
| rs757561444 | in-del | -/T | 0.000192141 | 0.00979968 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796933 | TTAAATATAACATTC[-/T]TATACTTTTGTTCTG | 27342 |
| rs757585407 | snp | A/C | 1.68838e-05 | 0.00290544 | intron-variant, missense | RABGEF1 | GRCh38.p7 | 7:66783675 | TAATTTTCCCAGCAG[A/C]AATTCAGGAAGCAAA | 27342 |
| rs757593893 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782165 | AGATAAAAAATATTT[C/T]AGAAAAGATGTTGCA | 27342 |
| rs757594911 | snp | C/T | 0.000411184 | 0.0143326 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773750 | AACTTACTGCAACCT[C/T]TGCTTCCTGGGCTCA | 27342 |
| rs757632355 | in-del | -/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749122 | CCTCCATACAGAGAT[-/G]GGCTGAGGGAATACC | 27342 |
| rs757645737 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713041 | GCTGGTCTCGAACTC[C/T]TGGGCTCAAGCGATC | 27342 |
| rs757684050 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729266 | TGACCTCCACCATTA[C/T]CACCATCCTCGCCTT | 27342 |
| rs757698237 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763734 | ATGAATGGAATCATA[C/T]AATGTGTGGTGTTCT | 27342 |
| rs757709721 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783311 | TTGTTATTCTATTTG[C/T]TGACTAGTTTTATAA | 27342 |
| rs757839138 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789410 | ATTTGAGGCCGGGTG[C/T]GGTGGCTTACGCCTG | 27342 |
| rs757840221 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711964 | ATTGCCAATACTACA[C/G]TGTCTTAATTACTAT | 27342 |
| rs757844103 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770055 | TATGTCTGTTGCTCC[C/G]TAACAGTTTCCTAAC | 27342 |
| rs757845830 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697320 | GGGCTTGCAGCGTGG[C/T]GTCTCACAAGTCTTG | 27342 |
| rs757926593 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701900 | ACTGTTTTTAAAAAT[C/T]GTGGTTAAGTATACA | 27342 |
| rs757956469 | in-del | -/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723823 | GACCTCAGGTGATCT[-/G]CCCACCTTAGCCTCC | 27342 |
| rs757957417 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686100 | CCTGGATCAAGACTG[C/T]GAAACCCCGTCTCTA | 27342 |
| rs757958623 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745762 | AACAGAGTGAGACTC[-/T]TATCTCAAAAAAAAA | 27342 |
| rs757965465 | snp | G/T | 4.95896e-05 | 0.00497919 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805402 | CACCAATCTGGTGAG[G/T]AAGTGAGTTCTTGGT | 27342 |
| rs757998030 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718813 | GGGTGAGCTGAAGAG[-/T]TTATATAAATTGTTA | 27342 |
| rs758043811 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696040 | CTGGGTGGGGCTGGA[C/T]GTGGGCCTTACAAGG | 27342 |
| rs758098680 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737421 | ACCACACCTGGCTAT[A/C]CTACGCAATACGAGA | 27342 |
| rs758125540 | snp | A/G | 1.64741e-05 | 0.00286998 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66795568 | TACCACAATGTGGCC[A/G]AAAGGATGCAAACTC | 27342 |
| rs758149912 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803163 | AGCAAAAATTATGTA[A/G]TTCACACAGTAGCCT | 27342 |
| rs758154363 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710086 | AGCCACGTGACTGGT[A/G]CCTTCTACATTGCAC | 27342 |
| rs758156409 | snp | C/T | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758852 | CCATGATAGGTGTTA[C/T]TTTTATTAAAAAACG | 27342 |
| rs758182028 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769781 | ACTTTCAATCCAGAC[C/T]CTGTAGCTTAGAGTT | 27342 |
| rs758211772 | snp | A/T | 1.64803e-05 | 0.00287052 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795637 | GGTATTGCACAGGGA[A/T]GACTGCTCAGTCTCT | 27342 |
| rs758232123 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693331 | TTTCCATTTCCCCTT[G/T]ATTGCAAACACGTTG | 27342 |
| rs758248518 | snp | C/T | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758251 | GGTTTGCATCCAGAG[C/T]CTTAAGAAAGAACAC | 27342 |
| rs758262530 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691715 | TGTGTTCAATAATTT[G/T]GCCAAACTGAAGGCT | 27342 |
| rs758262815 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746982 | TATTTTTAGTAGAGA[C/G]GGGGTTTCACCATGT | 27342 |
| rs758281481 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742701 | AGTCTCAACTGCCTG[G/T]GCTGAAGTGATCCTC | 27342 |
| rs758293253 | in-del | -/AAA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687484 | TCTGTTGTTTAAGCC[-/AAA]AAAAAAAAAAAAAGA | 27342 |
| rs758339585 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810899 | AAGATCTATTAAGCT[C/T]GACACATCTGTGTCA | 27342 |
| rs758343444 | snp | C/G | 0.00248447 | 0.0351577 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773923 | CGGCCGCCTTGGCCT[C/G]CCAGTGTGCTGGGAT | 27342 |
| rs758349980 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791354 | TATACTCCCTGGTGA[A/G]ATGGACTTTCTCAGA | 27342 |
| rs758401036 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771295 | AGGCGCCCGCCACCA[C/T]GCCTGGCTAATTTTT | 27342 |
| rs758406982 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775818 | TTTCTGCCTGAGAGC[C/T]TATTTGAGAGACAGC | 27342 |
| rs758513856 | in-del | -/CATT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783535 | GGAAAGTTGTCCAAC[-/CATT]CAAACATAAAATTAT | 27342 |
| rs758526436 | snp | C/G | 1.66054e-05 | 0.00288139 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66775276 | AGTCAGAGCAGCCAA[C/G]GGGCCCAATCCCTCA | 27342 |
| rs758586124 | in-del | -/TG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792997 | TACTGGAGCATAAAC[-/TG]TGCAGTAGAAATAGA | 27342 |
| rs758600218 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713266 | TCTGCCTCAGCCTCC[C/T]GAGTAGGTGGGACTA | 27342 |
| rs758603844 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776728 | AAAAAGATTGATTAC[A/G]TGATTAATTTGAAGT | 27342 |
| rs758605686 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798114 | AGAGCAAGACTCCTT[A/C]TCAAAAAAATAACAA | 27342 |
| rs758710439 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764922 | ATTCTTTTTCAGTAT[G/T]GTTTTGGCCATTCTG | 27342 |
| rs758723500 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690840 | TAAAATTCCAGCACT[C/T]TGGGAGGCTGAGGAA | 27342 |
| rs758743375 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771548 | TCCAGTGTCGGGAAG[C/T]TTTTCCCCTAAGTTT | 27342 |
| rs758779658 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700832 | GAGGACATCTCTGCA[A/G]AGGCCCCAGCGGCCC | 27342 |
| rs758799606 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799086 | GTAGCACTGCGTAAT[A/G]TCATTTCAGTCAGCA | 27342 |
| rs758836279 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772967 | CTAGTGAGCATAGGA[A/G]CTAATAAAATGCCAT | 27342 |
| rs758860255 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684145 | GCTGGGTCCTTATGT[A/G]GTTAAAATGGGTCTC | 27342 |
| rs758866283 | snp | A/G | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754932 | TAATCCCAGCACTTT[A/G]GGTGGCAAACCATGG | 27342 |
| rs758875543 | in-del | -/CT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751516 | TCAGAGAAGAAATCA[-/CT]CTTCCTTTTGCTAGG | 27342 |
| rs758882871 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795844 | AGGGCTGGAGCTGAC[A/G]AAAACATCTTAGGGC | 27342 |
| rs758888390 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715216 | CACTGCATCCTCAAA[C/T]TCATGGGCTCAAGTG | 27342 |
| rs758896306 | snp | A/G | 1.65228e-05 | 0.00287422 | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66799380 | TAATGAAGACATCCC[A/G]GAAGTGTCTGATATG | 27342 |
| rs758910896 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713589 | TGAGAATGAACATCC[A/T]TATCTTGTACCTTAA | 27342 |
| rs758949439 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759735 | CCAGATCTCACAAGC[A/G]CAGAACCACAGGGGA | 27342 |
| rs758973175 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699784 | CTTGAACCCAGGAGG[C/T]TGAGGCTGCAGTGAG | 27342 |
| rs758973241 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713896 | TCAGATATTGAACCA[C/G]CCTTGCATTGCTGAT | 27342 |
| rs758980884 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782765 | CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTTC | 27342 |
| rs758997094 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700300 | GCTCAGTCCTTAAAA[C/G]TCCATCGGCCTGAGC | 27342 |
| rs759023387 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729974 | CCAGGAGCCTTGTCC[C/T]CCTTACTTCAGATCT | 27342 |
| rs759030580 | snp | A/G | 1.82088e-05 | 0.00301729 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772117 | GTTGAACAGTGACGT[A/G]ACTGGATACATAGTT | 27342 |
| rs759079266 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783204 | AGTCTCCACATAAAC[A/G]CATTAACCTTTGCTT | 27342 |
| rs759089796 | in-del | -/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736002 | TTATTGAGTAGAGGT[-/G]GTTGCTGTCCACTGT | 27342 |
| rs759114588 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764555 | ATGAAAATTTTACCT[C/G]TACATTTTCTTCTGA | 27342 |
| rs759146521 | in-del | -/AG | 3.39709e-05 | 0.0041212 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775441 | GCCTGAGTGAGACAC[-/AG]AGGAGATCCCCAATG | 27342 |
| rs759172413 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741755 | CAGGCAGGTGTGAAA[C/T]TCCTGGCCTTAAGTG | 27342 |
| rs759191747 | in-del | -/CT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728712 | CACCTCAACTTTCAG[-/CT]CTGTCCTCACCTCCA | 27342 |
| rs759193528 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682636 | TCTGTGGTCGCGCGG[C/G]ACCCATCCCAGGACC | 27342 |
| rs759220974 | snp | A/G | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755381 | TTGGGAAGCTAAGGT[A/G]GAGAGGATCACTTGA | 27342 |
| rs759230216 | in-del | -/AG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777775 | TCCAGCCTAGGCAGC[-/AG]AGTGAGACACCAACA | 27342 |
| rs759241672 | snp | C/T | 1.64852e-05 | 0.00287094 | missense | RABGEF1 | GRCh38.p7 | 7:66809022 | CTCCTGATGCTTGCT[C/T]AGGCGTCAAGCAAAT | 27342 |
| rs759256033 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725532 | TCTTGTTTCTTTTTA[A/T]TGCCAATAACATTAC | 27342 |
| rs759263334 | in-del | -/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754005 | CAACGTACTAGGCCA[-/T]TTTTTTTTTTTTTTT | 27342 |
| rs759276531 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785173 | AATGAGTATACTAAA[A/G]TAAAGAGGTAATTAA | 27342 |
| rs759301524 | in-del | -/TAATGCA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777025 | GAGGATTCAGTGAGT[-/TAATGCA]TAATGCATGTAAAGA | 27342 |
| rs759329443 | snp | A/G | 3.29636e-05 | 0.00405964 | missense | RABGEF1 | GRCh38.p7 | 7:66809112 | AAGCCAAGAAACTGG[A/G]AAAAGACCTCATAGA | 27342 |
| rs759352563 | snp | C/T | | | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760535 | CACAACCTCTTCCTC[C/T]CGGGTTCAAGTGATT | 27342 |
| rs759395517 | snp | A/G | 1.65858e-05 | 0.00287969 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797541 | TGCTTTGTAGTTACT[A/G]CCTTCTAATGGAAGA | 27342 |
| rs759428930 | snp | A/C | 3.30726e-05 | 0.00406635 | missense | RABGEF1 | GRCh38.p7 | 7:66799348 | TGGGTTACGCCTCAG[A/C]TGCTGTGTGTCCCTG | 27342 |
| rs759431588 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772415 | TGACGTACCCACTGC[A/G]GGGCTTGGAAATGGC | 27342 |
| rs759460790 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694429 | ACCCGGGGAGTTGGA[A/C]GGAACATAAGGTCTG | 27342 |
| rs759469630 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684426 | CCAGCCTGGGCAACA[C/G]TGCAAGACTTCGTCT | 27342 |
| rs759475970 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797636 | CCTGCTTCCTTAGAG[C/T]GGAAGCAGCTCTGTT | 27342 |
| rs759476566 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793479 | TTTTTGAGCATTTCA[C/G]ATTTTTTATTTTTGG | 27342 |
| rs759479602 | in-del | -/TTT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738015 | TGGTTGTGTTTTTTG[-/TTT]TTTTTGTTTTTTTTT | 27342 |
| rs759513079 | snp | C/T | 1.65463e-05 | 0.00287626 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66771989 | CTACGGCAACCCTGC[C/T]TGGCAGGGTTTCTGC | 27342 |
| rs759530956 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743590 | ACTGCAAGCTCCCCC[-/T]TCCTGGGTTCACGCC | 27342 |
| rs759546774 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748275 | CAAAATAATGTGATC[C/T]GAGTACTTAGATCTC | 27342 |
| rs759548396 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719346 | AGTTGGGAACCATAG[A/G]TGCACGCCACCAAGC | 27342 |
| rs759561778 | snp | C/T | 3.58044e-05 | 0.00423095 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783639 | TGCATGGATCTTTTA[C/T]GTCATGAAACTTACT | 27342 |
| rs759591729 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696564 | GCATGATGGCGGGTA[C/T]CTGAATTCCCAGCTA | 27342 |
| rs759599807 | snp | A/G | 1.65108e-05 | 0.00287317 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66775368 | GAAATTCTTCAGTGC[A/G]TCTTCCAGGGTCGGA | 27342 |
| rs759603027 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735626 | CTTTGGTGCTGTTCT[C/T]GTGATGGTGAGTGAG | 27342 |
| rs759612621 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700631 | AAAAGGGGTTCGTGC[A/G]TAGCAGGGGGCCCAG | 27342 |
| rs759639195 | snp | C/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754992 | CCAGCCTGGGAAATA[C/T]AGCTAGATCCTGTCT | 27342 |
| rs759663645 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695819 | AAAAATACAAAAATT[A/G]CAGGGGTGTGGTAGC | 27342 |
| rs759672419 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794954 | AAACATGCATTAAAT[C/G]TATTTAAGAATACGT | 27342 |
| rs759683431 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802122 | TCATCATGTTGCCTT[A/G]GCTGCTCTTGAACTC | 27342 |
| rs759701927 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776803 | AAAAGGGGGGAAAAA[G/T]TAGTACCTGCCAGAG | 27342 |
| rs759708203 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715117 | CCTCCTCCAACTCCT[C/T]CTCTTCCTTTCTTCT | 27342 |
| rs759797421 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736732 | CAGGTGTGGTGGCTT[A/G]CGCCTGTAATCCCAG | 27342 |
| rs759808545 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797328 | AAAAAAAAAGAGAGA[A/G]AAAAAATATATATAT | 27342 |
| rs759815079 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709652 | TTAGCCAGGCATCTT[A/G]TAATCCCACCTACTC | 27342 |
| rs759826413 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767593 | CTAAACCACAAGGTG[A/T]TGCTACTAGGAGGTG | 27342 |
| rs759870522 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801443 | TTAAATTACTTTTGA[C/T]TATAGTTCCCCTGTC | 27342 |
| rs759901545 | in-del | -/AAAG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741994 | AAAAAAAAAAAAGAA[-/AAAG]AAAATTTGCCGGGCA | 27342 |
| rs759906949 | in-del | -/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696271 | GGTTTTACCATGTTG[-/C]CCAGGCTAGTCTCAA | 27342 |
| rs759963743 | snp | C/T | | | intron-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758541 | GCTCCCTCCTGGAAG[C/T]AGTGCTGGTGGTGGT | 27342 |
| rs759963860 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743671 | CATGCCTGGCTAATT[C/T]TTTCTATTTTTAGTA | 27342 |
| rs759975726 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704908 | GGCCTTGCAGCTGGC[C/G]TATATTTAGTTTTTT | 27342 |
| rs760034074 | snp | C/T | 3.29636e-05 | 0.00405964 | missense | RABGEF1 | GRCh38.p7 | 7:66809124 | TGGAAAAAGACCTCA[C/T]AGATTGGACAGATGG | 27342 |
| rs760046791 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775458 | AGGAGATCCCCAATG[C/T]TCATAAGCTCAGCTT | 27342 |
| rs760104519 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790573 | CCTTAGCGCCGCCCT[C/T]GTTGATGAGGTGAAG | 27342 |
| rs760150405 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720308 | GCTCAAGAAATTCTC[A/G]TGCCTCAGCCACCCC | 27342 |
| rs760156194 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745408 | AATACCTGTGTAAAC[C/T]TAACACCTGTGACTC | 27342 |
| rs760160316 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799659 | AAACTAAGGTCAAAT[A/G]CAGATAGAATAAATT | 27342 |
| rs760167141 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741847 | AACTGCTGTTAAAGA[C/G]TGTGTTCCGGCCGGG | 27342 |
| rs760169546 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690805 | AGGATTGTATAAGGC[C/T]AGGTGCGGTGCCTCA | 27342 |
| rs760226634 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800110 | TTGGAAAGGCTTGTT[C/G]ATGTAGACATTGTTA | 27342 |
| rs760257544 | snp | A/G | 1.64966e-05 | 0.00287194 | missense | RABGEF1 | GRCh38.p7 | 7:66809175 | ACATCGTTGAGAAAT[A/G]CCCACTGGAAATTAA | 27342 |
| rs760260710 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773866 | AGACAGGGTTTCACC[A/G]TGTTGCCCAGGCTGG | 27342 |
| rs760272394 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787811 | ACTGTATAGACCCAA[A/T]CAAGTGTTAACCTTT | 27342 |
| rs760280256 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785597 | ATAGCCTTTGTGGCC[A/G]GGTGCGGTGGCTCAC | 27342 |
| rs760391219 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714710 | GGAGGCCCAGGCGGG[C/T]GGATCATGAGGTCAG | 27342 |
| rs760419160 | snp | C/T | 8.23839e-05 | 0.00641757 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795620 | GCCATTGAGAGATTG[C/T]GGGTATTGCACAGGG | 27342 |
| rs760422934 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795070 | CGGGGTGGAGTTTTG[A/G]GAAGTTTGCACCATT | 27342 |
| rs760458063 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709813 | AGCAAATATTCCAGT[G/T]AAATCAGGTCATTGA | 27342 |
| rs760463787 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774368 | AGTACAGATCTGACA[A/G]CGATAACTCCTTGGA | 27342 |
| rs760491126 | snp | C/G | 3.30431e-05 | 0.00406454 | missense | RABGEF1 | GRCh38.p7 | 7:66799361 | AGATGCTGTGTGTCC[C/G]TGTTAATGAAGACAT | 27342 |
| rs760528152 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762533 | GAGGTCGAGTGTTGT[A/G]AGCCATGATCACACC | 27342 |
| rs760546177 | in-del | -/C | 1.73015e-05 | 0.00294116 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775215 | TCATTCTAATCCTCT[-/C]TTGAATTGCAGACTC | 27342 |
| rs760548188 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701517 | TTTTTTTTTTTTTTT[-/A]AATTTTTTGAGACAG | 27342 |
| rs760552253 | snp | A/G | 0.000190204 | 0.00975018 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773689 | GTTTGTTTTTGAGAC[A/G]GGGTCTTGCTCTGTT | 27342 |
| rs760560291 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696558 | AGCCAGGCATGATGG[C/T]GGGTACCTGAATTCC | 27342 |
| rs760570184 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807121 | GTTTGAGCGTAGCCA[C/T]GGTCACTGACAGTAG | 27342 |
| rs760581276 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696820 | AGAGCACATCTGGCC[C/G]CCCATCTGGTGGATG | 27342 |
| rs760581312 | snp | A/G | 1.67097e-05 | 0.00289043 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805114 | ATTCTTTTCTCCTGG[A/G]AAATATTGTCTTTTC | 27342 |
| rs760581515 | snp | G/T | 1.72636e-05 | 0.00293794 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775216 | CATTCTAATCCTCTC[G/T]TGAATTGCAGACTCC | 27342 |
| rs760613924 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761539 | ACACCCTCCAGGAAC[C/T]TGCACTGTGTTCAGC | 27342 |
| rs760642277 | in-del | -/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715388 | CTTTCACCTTGGCCT[-/C]CCAACATGTTGGGAT | 27342 |
| rs760642347 | in-del | -/AT | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758839 | GTACACATTAGTCCC[-/AT]GATAGGTGTTATTTT | 27342 |
| rs760666466 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711298 | TTGTATCTAAGAACT[C/T]TTTGCCTAACCTAAT | 27342 |
| rs760699846 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735754 | ATCCTTCTGCCATGA[C/T]TGTAAGTTTCCAGAG | 27342 |
| rs760725755 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767792 | TTCCTGATCTTGAAC[C/T]TGCCAGCTTCCTGCA | 27342 |
| rs760726344 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751637 | TCTGATTTGCCCTTA[C/G]TCCTAGCAGGTACCC | 27342 |
| rs760731584 | in-del | -/TGTGTGTGTG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702348 | GGCTATTGTTTTGTT[-/TGTGTGTGTG]TGTGTGTGTGTGTGT | 27342 |
| rs760731595 | snp | A/C | 1.6892e-05 | 0.00290615 | intron-variant, missense | RABGEF1 | GRCh38.p7 | 7:66783770 | ATAGAATTTCTCAAG[A/C]CCTTCCACAAGACAG | 27342 |
| rs760740556 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810847 | TTGGAATAAAACCAG[A/G]GTGGGTATAAAACTT | 27342 |
| rs760742145 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759297 | ATAAAGGTTAGTTGT[A/G]CATTGAGCAGATTCT | 27342 |
| rs760759429 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728322 | CTTGTGGAGAGCCAG[A/G]TGCTCTTCAGGGACC | 27342 |
| rs760779807 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769458 | CGCTCAAACATCTCA[A/G]TCTTTAGTTAGGCTT | 27342 |
| rs760780275 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703640 | TTTTTCTGGAACTCT[A/G]TTTCATTGGTCTATA | 27342 |
| rs760782624 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717809 | AAGTGATCCACTCGC[C/G]TTGGCCTCCCAAAGT | 27342 |
| rs760787817 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801723 | CTGGATCCCATTCTG[A/T]ATAGTACTCCACTGT | 27342 |
| rs760792589 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703591 | TCTTGACACCTTTTT[C/T]GGAAATCAGTTGACA | 27342 |
| rs760824547 | in-del | -/AAG | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755508 | AAAAAGCGTAAAGAA[-/AAG]AAATGCCTTTAACAG | 27342 |
| rs760846657 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758161 | CCAGGAATAGGAAGC[A/G]GACCGCCAAGAAGGA | 27342 |
| rs760928311 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766260 | GCTGCAGTGAGCTGT[A/G]ATCACGCCACTGCAC | 27342 |
| rs760932560 | in-del | -/ACACACACACGT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736936 | CACCTACGTATACAG[-/ACACACACACGT]ACACACACACGCACA | 27342 |
| rs760938245 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746190 | GATAAAGCTCCTAAA[A/G]TGCTTTAGGAAAACA | 27342 |
| rs760942497 | snp | A/G | 0.000934454 | 0.0215952 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66771935 | CCGAGGAATTCATGT[A/G]GATCAATCGGATCTC | 27342 |
| rs760953212 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66685640 | GTTGGGCACACAAGT[A/G]TTTAATGAGTATTTA | 27342 |
| rs760973061 | snp | A/C | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681634 | GTCTCGAACTCCTGG[A/C]CTCAAGCGATCCTCC | 27342 |
| rs760973240 | snp | A/G | 1.69507e-05 | 0.0029112 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808865 | TCCTAATATGACTGT[A/G]TTAACGTCCTCTTCT | 27342 |
| rs760983173 | snp | C/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758665 | GCTGTCTGTAGCTGT[C/G]ATGTCCAATCTGGGT | 27342 |
| rs760994135 | in-del | -/CTGT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732759 | TCTCTCGCTCTCTTG[-/CTGT]CTCTCTTTCTCACTC | 27342 |
| rs761128325 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694366 | GGCAGCAGTGATGGT[C/T]GGGAGAAGATGGAGC | 27342 |
| rs761148964 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724199 | CCTCTAGCTTTCATT[A/G]TTTCTGATAATAAGT | 27342 |
| rs761182031 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732763 | TCGCTCTCTTGCTGT[C/T]TCTCTTTCTCACTCG | 27342 |
| rs761191339 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763566 | ATTCTCCCTTTTGAA[G/T]TGCACACTTAAGTGA | 27342 |
| rs761200639 | snp | G/T | | | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66775334 | CCAACGAGAAGACCC[G/T]CAAGGTTACCACAGT | 27342 |
| rs761227269 | in-del | -/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721841 | TTTGTCTTTTTACTT[-/C]CTTGGTGCTTTGAAA | 27342 |
| rs761241583 | snp | A/T | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680619 | AATTTGAGAAACGAA[A/T]CAATTAATCTCCACT | 27342 |
| rs761244789 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810499 | GGAGTTATCCTCCTG[A/G]TGGTTAATATGGTGT | 27342 |
| rs761256606 | snp | A/G | 3.57967e-05 | 0.0042305 | utr-variant-3-prime | RABGEF1 | GRCh38.p7 | 7:66809302 | ACAATTTAGTGGAGA[A/G]TATTTATTTGAGCCT | 27342 |
| rs761273968 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691560 | CTTGGGATTTTTTCA[A/G]CTTTATGATAGAACA | 27342 |
| rs761274035 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709875 | CTAGGAGGTAATACT[A/G]GAAACAATTGGGTAT | 27342 |
| rs761285645 | snp | A/G | 1.64792e-05 | 0.00287042 | missense | RABGEF1 | GRCh38.p7 | 7:66808982 | GGCCAGACCTCTCCC[A/G]GGAAGCAAGAAGCTG | 27342 |
| rs761290016 | in-del | -/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804757 | AAAAAAAAAAAAAAA[-/G]TGTGGGCTTTACAGT | 27342 |
| rs761300031 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803888 | GTGAGATGCTGTCTC[-/A]AAAAAAAAAAAAAAA | 27342 |
| rs761307130 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733724 | ACAAAACAAAAAAAC[C/G]CTCCTAGGCCAGGTG | 27342 |
| rs761356764 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722272 | TGGTGAAACCCCACC[G/T]TTACTAAAAATACAA | 27342 |
| rs761366941 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788571 | CAATCAATTCAGTTT[C/G]TAAAAGACTTCTTAA | 27342 |
| rs761390819 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764630 | GAGTTAGTTTTTGTA[C/T]GTGGTATGAAGTAAG | 27342 |
| rs761410066 | in-del | -/TTCTT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766456 | CATTCTAGGACTCTA[-/TTCTT]TTCTTTTTTTCTACT | 27342 |
| rs761418865 | snp | A/G | 2.43046e-05 | 0.00348593 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797338 | AGAGAGAAAAAATAT[A/G]TATATCTTGATCTTT | 27342 |
| rs761447215 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774188 | ACCAAGTTCTATTTC[C/T]TCCAACTCAGAAAAG | 27342 |
| rs761459588 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763455 | CCTCCAGCTTCAAAA[C/G]CATCAATAGTGCTTT | 27342 |
| rs761491447 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751835 | AATTTGGATTGTGTC[C/T]TCAGGGGAAAACCAG | 27342 |
| rs761536227 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703256 | GGATTACAGGTATGA[A/G]CCACCGTGCCTGGCC | 27342 |
| rs761666343 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782764 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTT | 27342 |
| rs761687302 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737029 | GTGGGTGATATTATC[A/G]TCATTATATATATAT | 27342 |
| rs761689306 | snp | A/T | 1.6473e-05 | 0.00286988 | missense | RABGEF1 | GRCh38.p7 | 7:66805260 | CGGCGTCAGCGGATG[A/T]CTTCCTCCCCACCCT | 27342 |
| rs761810468 | snp | A/G/T | 4.95073e-05 | 0.0049751 | missense | RABGEF1 | GRCh38.p7 | 7:66809187 | AATACCCACTGGAAA[A/G/T]TAAGCCTCCGAATCA | 27342 |
| rs761838012 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803087 | AAAGAAAAATAAATA[A/G]ATCAATGTAACAATA | 27342 |
| rs761861841 | snp | G/T | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759339 | GCATTGTTAAGATTC[G/T]AAGCGTCTTCTCCCA | 27342 |
| rs761881367 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747857 | TTCCACATCTTGTTC[C/T]AGAAAGGGTTTGTAA | 27342 |
| rs761885810 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787895 | TAAATAACTTTTTTC[G/T]GTAAATTATTTATAT | 27342 |
| rs761903272 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804266 | TTTTTGTATTCTCAC[A/G]TTCAATACAAAGATG | 27342 |
| rs761909598 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688789 | AATGTATAGCTGTAA[A/G]CATCTACCTTTAAAA | 27342 |
| rs761916837 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707485 | ATCACCTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 27342 |
| rs761932982 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790990 | TGCACTGTGTGTCTC[A/T]TGTGCAACTTGTAAC | 27342 |
| rs761933492 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66685581 | CCAGCTAATTTGTAA[A/G]CAGGAATTCTGCACT | 27342 |
| rs761942187 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749285 | AGCAGGAGCCATGCA[-/T]TGTGTTAATGGAGAG | 27342 |
| rs761943122 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702324 | ATATTTGGGTGGCTT[C/T]CACCTTCTGGCTATT | 27342 |
| rs761964920 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695181 | GCCGGGCACGGTGGC[A/G]TGCACCAGTAATCCC | 27342 |
| rs761977413 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797021 | AAATATACTCTTGGC[C/T]GGGCATTCTGGCTCA | 27342 |
| rs762006539 | snp | C/T | 3.30349e-05 | 0.00406403 | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66799374 | CCCTGTTAATGAAGA[C/T]ATCCCAGAAGTGTCT | 27342 |
| rs762067576 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716804 | TGAGACAGGAGACAA[C/G]GTCTTGCTCTGTTGC | 27342 |
| rs762079350 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734723 | CAGGTGTGAGCCACC[A/G]TGCCTGGCCCCAAAG | 27342 |
| rs762093720 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779583 | AGGCTGAGATGGGAG[A/G]ATCATTTGTGCCTGG | 27342 |
| rs762116308 | snp | A/C | 1.70087e-05 | 0.00291617 | intron-variant, missense | RABGEF1 | GRCh38.p7 | 7:66783789 | TCCACAAGACAGGCC[A/C]AGAAATCTATAAACA | 27342 |
| rs762127620 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746446 | TAGTTAACCACCATA[C/T]CCAGCTAATTTTTTT | 27342 |
| rs762129027 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792272 | ACTTACCAACACAAA[C/T]CTGCCCTCACTTTGC | 27342 |
| rs762156726 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805011 | CTAAGTTATTATATA[A/C]TAAGTTAACTGCTGG | 27342 |
| rs762183065 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807315 | GCTGACGAACCCCAC[C/G]GGCACTCACAGTCTT | 27342 |
| rs762207761 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810754 | AACAACGTCACTTCA[C/T]ACAGGCAGCTGAGAA | 27342 |
| rs762237266 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747409 | ATGCTAGGCACAGAA[A/C]AACTCAGGAGGAATT | 27342 |
| rs762238764 | in-del | -/TGTGTGTG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702350 | CTATTGTTTTGTTTG[-/TGTGTGTG]TGTGTGTGTGTGTGT | 27342 |
| rs762239544 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778327 | GAATTTGAAGAATAT[C/G]TTCACATTCTTTTAG | 27342 |
| rs762289232 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694399 | GGATCAGTGAGGCAC[C/T]GTTAGGAGTGATGAA | 27342 |
| rs762315013 | in-del | -/AG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737443 | AATACGAGACTGGGT[-/AG]GGGGGGGCAGTCTAA | 27342 |
| rs762327932 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805052 | AATAAGGATTCCTTC[A/G]TAACTTTAGAGATAA | 27342 |
| rs762369569 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733525 | AACATGGTGAAACCC[C/T]CATCTCTACTAAAAA | 27342 |
| rs762389588 | snp | A/G | 1.6516e-05 | 0.00287362 | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66797498 | TCTTGCCATTCAAAA[A/G]AGAATCAGGTAGTTG | 27342 |
| rs762391805 | snp | A/C | 3.7022e-05 | 0.00430228 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771853 | GTAGAATGATAATTC[A/C]TTTTCAACAGCACTT | 27342 |
| rs762409328 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766258 | AGGCTGCAGTGAGCT[C/G]TGATCACGCCACTGC | 27342 |
| rs762413243 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724378 | TTTATTTTTTTTTTT[G/T]GAGACGGAGTCTCGC | 27342 |
| rs762421989 | snp | C/T | 3.29598e-05 | 0.00405941 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795476 | CTTCTGCACTTTGTT[C/T]AGCTACAAGCAGCCT | 27342 |
| rs762456725 | in-del | -/AGTA | 3.30584e-05 | 0.00406548 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805400 | TTCACCAATCTGGTG[-/AGTA]AGTGAGTTCTTGGTG | 27342 |
| rs762512801 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781668 | ATACACATGTGCGGT[A/G]GTCAGCCACACTCAA | 27342 |
| rs762519718 | in-del | -/CT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732714 | TCTCTCTCTCGCTCA[-/CT]CTCTCTCTCGCTCTC | 27342 |
| rs762549143 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767195 | TTAATAGAGACGAGG[-/T]TTTTGCCATGTTGGC | 27342 |
| rs762600300 | in-del | -/TT | | | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811200 | CCCACAAAAGCTGAC[-/TT]TTTTGGGTCTCTTAC | 27342 |
| rs762619395 | in-del | -/TTTTC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744026 | TTATTTGCTTTTTTC[-/TTTTC]TTTTCTTTTCTTTTC | 27342 |
| rs762665178 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722620 | AAGATTTATGCTTAC[C/G]TTTTCTTCTAAGAGT | 27342 |
| rs762668681 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700224 | CAGGGCACCCAGCCA[A/G]GCCCCACTGCGATGG | 27342 |
| rs762670099 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693637 | CCACACTTACCAGTG[C/T]TCAGAAACATTGAGA | 27342 |
| rs762673434 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805912 | ATCACACCGGGCCAA[-/T]TTTTTTTTTTTTTTG | 27342 |
| rs762674322 | snp | C/T | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680674 | AATTAGGGCCGGGCG[C/T]GGTGGCTCACGCCTG | 27342 |
| rs762677549 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690034 | TTGCATTGATAACTA[C/G]AGCCAGACAAAGGCA | 27342 |
| rs762708065 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807630 | TTCAGAGCTACTTCC[C/T]CTTCAGATGTTTGTT | 27342 |
| rs762728773 | snp | A/T | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760312 | TGCACTTTTTAGAAA[A/T]CTCAACATGTTGCTC | 27342 |
| rs762742859 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688966 | GGCATGGTGGTGCAG[A/G]CCTGTAATCCCAGCT | 27342 |
| rs762759521 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794382 | GCTGGCCTCAAACTC[C/T]TAGGCTCAATCGATC | 27342 |
| rs762764021 | snp | C/T | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681340 | AATTTGTGACTCAAC[C/T]ATTCATACTTTGTGA | 27342 |
| rs762790787 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729816 | CTGCCTTGTGGAGCA[C/T]GTCTGCCTGTGAGCT | 27342 |
| rs762792179 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804472 | AGGCACGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 27342 |
| rs762793656 | snp | A/G | 0.000107949 | 0.00734593 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783627 | AAAGTAATTCCATGC[A/G]TGGATCTTTTATGTC | 27342 |
| rs762814115 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785033 | TTAGTGTATGTATAC[A/T]GTAGTACATATAGCA | 27342 |
| rs762861633 | in-del | -/TTTC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744038 | TTTCTTTTCTTTTCT[-/TTTC]TTTTTTTTTTTTTTA | 27342 |
| rs762863506 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699295 | TCTGTTCCCCTAGAC[C/T]GGGAGACAAAGGACT | 27342 |
| rs762923163 | snp | C/T | 1.85765e-05 | 0.00304761 | utr-variant-3-prime | RABGEF1 | GRCh38.p7 | 7:66809332 | TAAATTGTAGGTAGC[C/T]CTTACTACACTCAAC | 27342 |
| rs762927666 | in-del | -/AG/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796248 | AGTTTAAAAAAAAAA[-/AG/G]GAGCTTCAAGTTTTT | 27342 |
| rs762944831 | snp | A/T | 1.94414e-05 | 0.00311775 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797349 | ATATATATATCTTGA[A/T]CTTTTCTCTGTCTGG | 27342 |
| rs762987504 | snp | A/G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792566 | TTAGGGATCCTTATT[A/G/T]GACAGTAAGCAGTCT | 27342 |
| rs762992815 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728849 | TCACCTACACCTACA[C/T]GTCTATCCTCACCTC | 27342 |
| rs763021212 | snp | A/G | 3.29495e-05 | 0.00405877 | missense | RABGEF1 | GRCh38.p7 | 7:66805184 | CCTCGAGACAAGCTG[A/G]CCTGCATCACCAAGT | 27342 |
| rs763029512 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708382 | AACCTTCGCTTCCTG[C/G]GTTCAAGTGATTCTC | 27342 |
| rs763030611 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722010 | AAAAAATCAAAAAAA[C/T]TAGCTGGGCATGGTA | 27342 |
| rs763051924 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793418 | CATGAGGCCAGGTGT[A/G]GAATTTCCCACTTGT | 27342 |
| rs763073454 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707635 | GGAAGTTGCAGTGAG[C/G]CGAGACTGCACCACT | 27342 |
| rs763109276 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735493 | TAAAATGGACTTCTG[A/G]GAGGTTGAAATGGTT | 27342 |
| rs763124689 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695599 | TTGGAGAGAGTGGGT[C/T]GTGAGAAAGTGAGGG | 27342 |
| rs763128405 | in-del | -/T | 1.8433e-05 | 0.00303581 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772131 | TGACTGGATACATAG[-/T]TCTGTCACCGTCTAA | 27342 |
| rs763142141 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799166 | CTAGCTGCTTCATCA[C/T]GTCATTAGAGCTCGT | 27342 |
| rs763143344 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726014 | GGTCAGCAGCCATGG[C/G]CCTGGGTCCTAAGGC | 27342 |
| rs763145170 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805558 | CACAAGGACCAGGCC[A/G]TACAGACACTCCGCC | 27342 |
| rs763147335 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720023 | AAGATCAAGTGAAAT[A/G]CGTCCCAGAAATACA | 27342 |
| rs763203877 | snp | C/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755837 | TTGCTCTGCTCATTC[C/T]AGCAGCAATCAACTC | 27342 |
| rs763219481 | snp | C/T | | | intron-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811715 | AATATAGAGCTATTA[C/T]TGTCTGTTGGTGAGG | 27342 |
| rs763250968 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800411 | CTTTCTCGGGTTCTG[C/G]TTCTCTTTATCTTCC | 27342 |
| rs763286429 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698238 | GAGCCTCACCAGTGC[A/G]TGCACAGCAAGGCCA | 27342 |
| rs763306832 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66685702 | CTTTGATTTTTGTTG[C/G]TGGTTTTCAGTGAAC | 27342 |
| rs763311708 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784662 | TAGCTGGGGTCAGCA[A/G]TCACTAGGCTAATAA | 27342 |
| rs763368084 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726970 | GATTGCGCCATTGCA[C/T]TCCAGCCTGGGTGTC | 27342 |
| rs763380938 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730525 | ATGCAGATTACCTGA[C/G]CTCATTCACATATAG | 27342 |
| rs763383068 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767529 | AACTTTTAAGATGGC[C/T]GCTATGGTCTGAATC | 27342 |
| rs763408681 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716082 | TTCTCCTCAAGTTCT[C/G]TCAGTTTTGCTGTAT | 27342 |
| rs763475392 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766421 | TCTTACTATAGGATG[C/T]AGTAGATGGTCTTTA | 27342 |
| rs763537599 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772782 | CCGGGCATGGTGGTA[C/T]GCATTTGTTATCCCA | 27342 |
| rs763545595 | snp | A/C | | | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757256 | TATTATGACTGATAT[A/C]TTTTTTATACTTTCT | 27342 |
| rs763564368 | snp | C/T | 1.64963e-05 | 0.00287192 | missense | RABGEF1 | GRCh38.p7 | 7:66809177 | ATCGTTGAGAAATAC[C/T]CACTGGAAATTAAGC | 27342 |
| rs763580922 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731953 | CTCCATCCACTCCCC[C/G]CAGGGCCCATGGGGG | 27342 |
| rs763612328 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807252 | AGAGTCTGTCTCCTA[C/T]ACCCATTGCTCCAAT | 27342 |
| rs763632120 | snp | C/T | | | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760731 | ACAGGCATGAGCCAC[C/T]GCACCCAGCCAGCAT | 27342 |
| rs763644719 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787831 | GTTAACCTTTCCCAT[-/A]AATAACTAGAAAACC | 27342 |
| rs763645596 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720346 | AGGACTACAGGCATG[C/T]ACCACCACGCCCAAC | 27342 |
| rs763659726 | in-del | -/TTG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770970 | TCGGATTATTTGGGT[-/TTG]TTGTTGTTGTTGTTG | 27342 |
| rs763669769 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690811 | GTATAAGGCCAGGTG[C/T]GGTGCCTCACCCCTA | 27342 |
| rs763713060 | snp | C/G | 1.6473e-05 | 0.00286988 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66795514 | TCTCTGTTTCAGGAT[C/G]TAAGCATTGAAGAAC | 27342 |
| rs763714596 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744061 | TTTTTTTTTTAAGAC[A/G]GAGTCTTGATCTGTG | 27342 |
| rs763749327 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735885 | TGCAAGAACAAACGA[A/C]TACAGAGGCCTGTAG | 27342 |
| rs763751150 | snp | A/G | 0.00136121 | 0.0260528 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773722 | CCTGGCTGGAGTGCA[A/G]TGGTGCAATTTCAAC | 27342 |
| rs763776728 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731080 | TGTACCACATTTCAA[G/T]GGGGCACACAGGGAC | 27342 |
| rs763790451 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727335 | TGAATTGGGGGTTCT[C/T]TGGACTCAGGGCCTA | 27342 |
| rs763797101 | in-del | -/T | 0.0137625 | 0.0818036 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796898 | CACCCAGCTGGTAAG[-/T]TTTTTTTTTAAGCGT | 27342 |
| rs763828112 | in-del | -/TTTG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791173 | CGGATTTCTGGCTTT[-/TTTG]TTTGTTTTTGGAGAT | 27342 |
| rs763829170 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761541 | ACCCTCCAGGAACCT[C/G]CACTGTGTTCAGCTG | 27342 |
| rs763835000 | in-del | -/GT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750157 | TTTTGTCTGATGAGA[-/GT]GTAGATTTTATTTGT | 27342 |
| rs763855690 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701996 | AATATTGTGCAAATA[G/T]CATCACTACCATCAA | 27342 |
| rs763867240 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805809 | GAGTGCAGTGGTACA[A/G]TCATAGCTCACTGCA | 27342 |
| rs763872526 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721214 | ATGAGCCACTGTGCC[C/T]GGCCAAAAGAAAGCC | 27342 |
| rs763905915 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731010 | AGCGCAGGGATTCGG[A/G]GCCAGGCTGCGGGCC | 27342 |
| rs763964269 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709824 | CAGTTAAATCAGGTC[A/G]TTGATTTTGACTAGA | 27342 |
| rs763987038 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707928 | GACATTAATATAGCC[-/A]CTCTAGCTCTCTTTT | 27342 |
| rs763997911 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781292 | AAAAGAAAAAAAAAT[G/T]AAAACAGTAGTGTTA | 27342 |
| rs763999528 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767840 | CTGTTTTTTATAACC[G/T]ACCCAGTTTATGGTA | 27342 |
| rs764021321 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749961 | CGTGGGCGACAGAGC[A/G]AGACTCCATCTCAAA | 27342 |
| rs764035454 | snp | C/G | | | intron-variant, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66685664 | GTATTTAACTGATTT[C/G]ATAAGAATAAATTCA | 27342 |
| rs764063500 | snp | C/G | 1.70298e-05 | 0.00291798 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66775230 | CTTGAATTGCAGACT[C/G]CAGCGGGAGGAAGAA | 27342 |
| rs764076933 | snp | C/T | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681972 | GAGGCTACCCTCTTC[C/T]ATTTGCTCTTGGGCG | 27342 |
| rs764085674 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780023 | CTAGTAGAGTTAATC[C/T]TCATTTACATTTTAA | 27342 |
| rs764125936 | snp | A/G | 1.64822e-05 | 0.00287068 | missense | RABGEF1 | GRCh38.p7 | 7:66809125 | GGAAAAAGACCTCAT[A/G]GATTGGACAGATGGA | 27342 |
| rs764134976 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703856 | ATTTTGATAGGGATT[A/G]CACTGAATCTGTAGA | 27342 |
| rs764135134 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717896 | ACTAGCTCTTTCTTC[A/G]GTCATGCACATTCTG | 27342 |
| rs764174079 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683537 | ACAGTGTGGTAAGGA[A/G]TGTGAGCTAAGATGG | 27342 |
| rs764215188 | snp | A/C | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758255 | TGCATCCAGAGCCTT[A/C]AGAAAGAACACTAAT | 27342 |
| rs764220628 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745641 | AGGCATGGTGATGTG[C/T]GCCTGTGATCTCAGC | 27342 |
| rs764228942 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704956 | TCTTCCAAAATGGCT[A/G]TACCAATTTGCATTC | 27342 |
| rs764284759 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801730 | CCATTCTGAATAGTA[C/G]TCCACTGTGTATGTG | 27342 |
| rs764302400 | in-del | -/AGG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736437 | ATAGACAGAAGAAGA[-/AGG]AGGGGAGTGGTAAGA | 27342 |
| rs764303046 | in-del | -/GGGG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737046 | ATTATATATATATGA[-/GGGG]GGGGGGAGAGAGAGA | 27342 |
| rs764333563 | in-del | -/TTTTCTTTT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744037 | TTTTCTTTTCTTTTC[-/TTTTCTTTT]TTTTTTTTTTAAGAC | 27342 |
| rs764376530 | in-del | -/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723702 | CTCCTGCCTCAGCCT[-/C]CCTGAGTAGCTGGGA | 27342 |
| rs764379118 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790804 | CTGATTTTTAGTACC[G/T]CATGTTTAATAATTC | 27342 |
| rs764401615 | snp | C/T | 1.64741e-05 | 0.00286998 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799276 | TGACAAGACAAATGG[C/T]CACAGTTTATCCTTG | 27342 |
| rs764454791 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763604 | TACCACAGCCAACTT[G/T]AGAACATTTTCATCA | 27342 |
| rs764478937 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789249 | TAGCAAATAGGCTTT[A/G]ATTATTGTGAGAACT | 27342 |
| rs764496663 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764558 | AAAATTTTACCTCTA[C/T]ATTTTCTTCTGAGAG | 27342 |
| rs764524442 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808829 | AAGATTTTTACAAAT[A/C]GACTCGAGTATGCAT | 27342 |
| rs764557581 | in-del | -/TGTGTGTGTG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702356 | TTTTGTTTGTGTGTG[-/TGTGTGTGTG]TGTGTGTGTGTGTGT | 27342 |
| rs764571786 | snp | C/T | 3.38198e-05 | 0.00411202 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808870 | ATATGACTGTATTAA[C/T]GTCCTCTTCTTGTAG | 27342 |
| rs764599241 | snp | C/T | 1.68997e-05 | 0.00290682 | intron-variant, missense | RABGEF1 | GRCh38.p7 | 7:66783776 | TTTCTCAAGACCTTC[C/T]ACAAGACAGGCCAAG | 27342 |
| rs764646351 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810561 | TGATGTTAACTAAAA[C/T]GAGTTAAATATTTAG | 27342 |
| rs764653802 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692952 | TTCAGGTAATACCAG[A/G]CTCAAGGCCCCCCAT | 27342 |
| rs764678263 | snp | C/T | 2.31919e-05 | 0.0034052 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797341 | GAGAAAAAATATATA[C/T]ATCTTGATCTTTTCT | 27342 |
| rs764690179 | in-del | -/AAGGGTAGGTTG | 1.89698e-05 | 0.00307969 | intron-variant, cds-indel | RABGEF1 | GRCh38.p7 | 7:66783837 | AGGAATGCATTACAA[-/AAGGGTAGGTTG]AAGGGTAGGTTGAGA | 27342 |
| rs764734586 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722831 | CTACAACAGGCAGCT[C/G]AGATTTTGATAAGGA | 27342 |
| rs764740758 | in-del | -/AGCC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778055 | CACTTAATATAACTT[-/AGCC]AGGTAAATTTTGCAT | 27342 |
| rs764764864 | snp | A/G | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680640 | AATCTCCACTTTACC[A/G]ATAATGAGCAAGAAC | 27342 |
| rs764765580 | snp | C/T | 1.86166e-05 | 0.00305089 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771850 | TTAGTAGAATGATAA[C/T]TCATTTTCAACAGCA | 27342 |
| rs764783646 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66750126 | GTTGCAGTTGGGGTT[C/G]TATTGAGAATGTAGA | 27342 |
| rs764795487 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711134 | CACTGCACTCCAGCC[C/T]GGTTGACAGAGTAAG | 27342 |
| rs764803215 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691642 | CCTGTTTTTCAATTT[C/T]AGTAGCGTATCCAAT | 27342 |
| rs764833131 | snp | C/G | 1.64738e-05 | 0.00286995 | missense | RABGEF1 | GRCh38.p7 | 7:66805350 | CGCGCTTCTGCAATC[C/G]AAGCCGACTGATGAC | 27342 |
| rs764844769 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807767 | CAACTCCACACACAC[C/G]ATGAGCCAGATGGTG | 27342 |
| rs764852730 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803201 | AAGGGAATAAAAGCA[C/T]TCAAAAGTTAAAATA | 27342 |
| rs764872057 | snp | A/C | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754965 | GGATTGCTTGAGGCC[A/C]GGAGTTCGAGACCAG | 27342 |
| rs764878927 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777793 | TGAGACACCAACATT[-/A]AAAAAAATTAATTAA | 27342 |
| rs764915272 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780249 | ACTACCTCATAGTCA[A/G]TTGTTAATAGTCAAC | 27342 |
| rs764928190 | in-del | -/CT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732698 | CTGCGCTCTTGTGCT[-/CT]CTCTCTCTCTCGCTC | 27342 |
| rs764929169 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716751 | TTGGATTTAGGTCTA[C/T]CATTTTGTTATTTTC | 27342 |
| rs764933677 | in-del | -/GGGA | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759676 | AGTGTCTCCCCTAGT[-/GGGA]GGGAGCAGGAGCAAG | 27342 |
| rs764940565 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733329 | AGGCTGCTGTGCACC[-/A]ATGTGACACTGGTGT | 27342 |
| rs764950499 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769691 | TGCTAGAAGACAGAA[C/G]TCTACATCTCAAGTT | 27342 |
| rs764960122 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781498 | GTATTTCTCCTAATT[A/G]GGTTATCCCTCCCCT | 27342 |
| rs764995525 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795215 | TTTTCTTCCTTTTCA[A/C]CTAATAAAACCCTGT | 27342 |
| rs765039216 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808712 | AGTGTATAGGAAGCA[C/T]GACCGGGGATAGGAG | 27342 |
| rs765066720 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788169 | AATAAACTTGGGGCT[A/G]GGCGAGGTTGCTCAC | 27342 |
| rs765123036 | in-del | -/C | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681411 | TTTTTTTTTTTTTTT[-/C]TTTTTGAGACAGGGT | 27342 |
| rs765128593 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688859 | GCATTTTGGGAGGCC[A/G]AAGCGGGAGGATCAC | 27342 |
| rs765134386 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801834 | TGTGGCTATGGGGGC[A/G]GTGGTTCTTAGCCAG | 27342 |
| rs765147836 | snp | C/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758711 | CCTTCTACCGTAACA[C/G]CTGTCACCACCACCA | 27342 |
| rs765162911 | snp | C/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739616 | GCAGTAAGCCGAGAT[C/T]GCACGACTGAACTCC | 27342 |
| rs765179860 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803092 | AAAATAAATAGATCA[A/G]TGTAACAATAATTAT | 27342 |
| rs765183210 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746768 | AGCTGGGAATATGGG[C/T]TCCTGCCACCACGTC | 27342 |
| rs765187274 | snp | C/G | 1.64738e-05 | 0.00286995 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795504 | CCTCTTTGTCTCTCT[C/G]TTTCAGGATCTAAGC | 27342 |
| rs765194892 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712554 | CAGCCCACTGCAGCC[C/T]CGACCTCCCGGGCTG | 27342 |
| rs765206054 | in-del | -/T | 3.31296e-05 | 0.00406985 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805133 | TATTGTCTTTTCTGC[-/T]TTGTAGATATCATTG | 27342 |
| rs765210474 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771018 | TGTAGGAGTTCCTTC[A/G]TATTTTAGATATTAA | 27342 |
| rs765226604 | snp | C/T | 3.29576e-05 | 0.00405928 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795631 | ATTGCGGGTATTGCA[C/T]AGGGATGACTGCTCA | 27342 |
| rs765281564 | snp | A/T | 3.30366e-05 | 0.00406413 | missense | RABGEF1 | GRCh38.p7 | 7:66799375 | CCTGTTAATGAAGAC[A/T]TCCCAGAAGTGTCTG | 27342 |
| rs765344010 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759344 | GTTAAGATTCGAAGC[A/G]TCTTCTCCCAGCAGA | 27342 |
| rs765360442 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694404 | AGTGAGGCACCGTTA[A/G]GAGTGATGAACCCGG | 27342 |
| rs765381682 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733831 | AACATAGTGAAACCC[C/T]GTCTCTACCAAAAAT | 27342 |
| rs765398432 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745691 | CAAGAATCTCTTGAT[C/T]CCGGGAGGCGGAAAT | 27342 |
| rs765427915 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771167 | CTTTTGAGACAGAGT[C/G]TTGCTCTGTCACCCA | 27342 |
| rs765464421 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766399 | TCTTAATGTTAGTAT[A/C]TTTATCTCTTACTAT | 27342 |
| rs765475278 | in-del | -/TG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703660 | ATTGGTCTATATGTC[-/TG]TCCTTATGGCAGTAT | 27342 |
| rs765494278 | snp | A/G | 1.64849e-05 | 0.00287092 | missense | RABGEF1 | GRCh38.p7 | 7:66805161 | TTGAAATGGATTCCA[A/G]GCGTGTGCCTCGAGA | 27342 |
| rs765531571 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729463 | AACCTCACTTCTGTC[C/T]TCCCCTTCCTCCTGC | 27342 |
| rs765536637 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683916 | CAGCTGATTTTTAAA[G/T]ATTTTGTAAAGATGT | 27342 |
| rs765552754 | snp | C/T | 0.000262778 | 0.0114595 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773786 | TCCTCCTGCTTCAGC[C/T]TCCCAAGTAGCTAGG | 27342 |
| rs765580340 | snp | A/G | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754745 | ATAAATACATTTCAC[A/G]TCTAGGCATTGCGTT | 27342 |
| rs765589810 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798027 | GAGGCTAAGGCACGA[C/G]AATGGCTTGAATCCA | 27342 |
| rs765591224 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700762 | TGCCTTGTCTCTTTC[C/T]ATCCAGGGCCTTGGG | 27342 |
| rs765618975 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792290 | GCCCTCACTTTGCCC[C/G]TTTGGCAAACACTGT | 27342 |
| rs765625657 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751032 | TTCCCTCTTTTTTTC[-/T]TTTTTTTTTTTTTTG | 27342 |
| rs765656729 | snp | A/G | 3.29527e-05 | 0.00405898 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795484 | CTTTGTTCAGCTACA[A/G]GCAGCCTCTTTGTCT | 27342 |
| rs765676196 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713765 | TTTCTGCATATGATA[C/T]ATTGATACGTTGATA | 27342 |
| rs765682736 | snp | A/G | 3.42513e-05 | 0.00413817 | intron-variant, missense | RABGEF1 | GRCh38.p7 | 7:66783798 | CAGGCCAAGAAATCT[A/G]TAAACAGACCAAGCT | 27342 |
| rs765688146 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683915 | CCAGCTGATTTTTAA[A/G]GATTTTGTAAAGATG | 27342 |
| rs765690941 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734743 | TGGCCCCAAAGGAGC[A/C]CTCCTGTGGGAGACC | 27342 |
| rs765790023 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798859 | CCCGGCTGCTTGGGA[A/G]CCTGAGGCAGGAGAA | 27342 |
| rs765805369 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725891 | CCTTCCATGTGAAGA[C/T]CCAATCAGAGGGGGA | 27342 |
| rs765828930 | snp | C/T | 0.000148833 | 0.00862521 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66771977 | AGGATGTGGTTACTA[C/T]GGCAACCCTGCCTGG | 27342 |
| rs765868940 | in-del | -/TCAC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796622 | TGTCGAGACAGAATA[-/TCAC]TCTGTCGTCCAAGCT | 27342 |
| rs765878210 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713080 | TCAGCTTCCCAAAGT[A/G]CTGGGATTATAGGCA | 27342 |
| rs765887682 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722678 | TCTATAAAACATCAC[A/T]ACTATGATGTTTTCA | 27342 |
| rs765928131 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807894 | TCCTGGTCTCAAGCA[A/G]TCCTCCCACCTCGGC | 27342 |
| rs765938074 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699296 | CTGTTCCCCTAGACC[A/G]GGAGACAAAGGACTG | 27342 |
| rs765941211 | in-del | -/GAGA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682907 | TCACGGCAGTTTAGG[-/GAGA]GAGAGGGAAGGACTC | 27342 |
| rs765983496 | in-del | -/TTTTTG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723571 | AAACAATTACTGTTT[-/TTTTTG]TTTTTGTTTTTGTTT | 27342 |
| rs766003196 | in-del | -/TCC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728684 | CCACCTTCACCTCCA[-/TCC]TCATCATCCTCACCT | 27342 |
| rs766004675 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796377 | AGCTCTACGATGTTA[C/T]GGTAAACCTCAGAAA | 27342 |
| rs766029268 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769857 | TACCTTCTGTCTGTG[C/G]TACATCATTCATATT | 27342 |
| rs766056183 | snp | C/G | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66738887 | CCACCATCCAAGGTA[C/G]TACTGTAAATAATTA | 27342 |
| rs766085321 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782551 | TCGTAGCTCACTGCA[A/G]CGTCAAACTCCTGGG | 27342 |
| rs766112772 | in-del | -/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714294 | TGTGAGTTTTGGTAG[-/C]TTTGTGGTTTTTCAG | 27342 |
| rs766116660 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771137 | AGATATTTAATTTTT[A/T]AAAATTTTTTATTTC | 27342 |
| rs766118419 | snp | C/G | 1.67894e-05 | 0.00289731 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808876 | CTGTATTAACGTCCT[C/G]TTCTTGTAGTGCTGT | 27342 |
| rs766159166 | snp | G/T | 1.64852e-05 | 0.00287094 | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66809017 | TTGGTCTCCTGATGC[G/T]TGCTTAGGCGTCAAG | 27342 |
| rs766173065 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734598 | ACCATGCCTGGCTAA[-/T]TTTTTTTTTTTTTTT | 27342 |
| rs766205289 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797788 | GGGACTGTGTTCTTG[A/G]TCCATTACCATCTCC | 27342 |
| rs766258194 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719266 | CGCAGTCTGAACCAC[A/G]AATGGAGAGCTTCTC | 27342 |
| rs766298816 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778735 | AAGGGCCCCTTCAAT[A/G]TTTTGGGGACATTTC | 27342 |
| rs766306493 | snp | G/T | 1.65556e-05 | 0.00287707 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797526 | TTGCTTATTTTGTTT[G/T]GCTTTGTAGTTACTA | 27342 |
| rs766310233 | snp | C/T | 1.84756e-05 | 0.00303932 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771854 | TAGAATGATAATTCA[C/T]TTTCAACAGCACTTT | 27342 |
| rs766337720 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695610 | GGGTCGTGAGAAAGT[G/T]AGGGATTAGAAGTGT | 27342 |
| rs766349526 | in-del | -/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693047 | GGAAAAAAGCAGTGA[-/G]CCGGCTGGTCCCGTG | 27342 |
| rs766359387 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804504 | TTTTGGGAGGCCAAG[A/G]TGGGCGGATCACCTG | 27342 |
| rs766407821 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770354 | AGAATGAAGACCATG[G/T]GGTTTCAGTTTGAAC | 27342 |
| rs766416567 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683110 | TGGCTTGGAGAGCTA[C/T]TTTCCCCTCTCTAAA | 27342 |
| rs766417226 | snp | C/T | 1.65721e-05 | 0.0028785 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66775285 | AGCCAAGGGGCCCAA[C/T]CCCTCACATTCTCCA | 27342 |
| rs766429805 | in-del | -/T | 3.35962e-05 | 0.00409841 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775411 | AATGTTCTGATACTC[-/T]TTTTTTTCTTCTCTG | 27342 |
| rs766452767 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718218 | GGCGTGGTGGTGCAC[A/T]TCTGTAATCCCAGCT | 27342 |
| rs766480206 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745793 | AAAAAAAAAGTGATC[A/G]CACTAAAACCAAGAG | 27342 |
| rs766505430 | in-del | -/AAAAC/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788460 | AAAAAAACAAAAAAC[-/AAAAC/C]AAAACAAAACAAAAC | 27342 |
| rs766544005 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799135 | GTGATAAATGCAGAA[C/G]TCTCATTTTAGGATC | 27342 |
| rs766558818 | snp | C/T | | | intron-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811775 | TTTGGTTTTGAATTT[C/T]ATTCTGCTACTTATT | 27342 |
| rs766591844 | in-del | -/ACATC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774809 | TAAGACCTCACCCAA[-/ACATC]ACCGTTGTAAAGCCT | 27342 |
| rs766592764 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696833 | CCCCCCATCTGGTGG[A/C]TGGTTTCTGAATAAG | 27342 |
| rs766616613 | snp | C/T | 6.60142e-05 | 0.0057448 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66775359 | CACAGTGAAGAAATT[C/T]TTCAGTGCATCTTCC | 27342 |
| rs766621206 | snp | A/G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728274 | CATTAGCTAAGCTTG[A/G/T]GGGGGCCACTGGGTC | 27342 |
| rs766634687 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684212 | GCACTTTGGGAGGCC[A/G]AGGCGGTTGGATCAC | 27342 |
| rs766638835 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694776 | AGGGCGGAGCCTCCG[A/G]TGATGCCAGCATCAC | 27342 |
| rs766692828 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766466 | CTCTATTCTTTTCTT[C/T]TTTTCTACTTGTTAT | 27342 |
| rs766714840 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742288 | CTGATTCATATCCGC[A/T]GGATTAAGAAATGTT | 27342 |
| rs766732720 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713909 | CAGCCTTGCATTGCT[C/G]ATATAAAACTGCCTG | 27342 |
| rs766738273 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743328 | AAAAAGAAAAAAATT[-/T]AAAAAAAAAAAAAAG | 27342 |
| rs766768049 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66685844 | TTTAATTTCTGGCAC[A/G]TGGGGTTTTATTGGC | 27342 |
| rs766777924 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800420 | GTTCTGCTTCTCTTT[A/G]TCTTCCCGTGTCAAC | 27342 |
| rs766822247 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702267 | ATAATATTTCATTGT[A/G]TGGATAGACCACAAT | 27342 |
| rs766825667 | snp | G/T | 1.64746e-05 | 0.00287002 | missense | RABGEF1 | GRCh38.p7 | 7:66805187 | CGAGACAAGCTGGCC[G/T]GCATCACCAAGTGCA | 27342 |
| rs766847409 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727028 | TAAAATAAAATATAA[A/T]ATGGACTGTGGAAAT | 27342 |
| rs766908515 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691862 | AGATCAAGACCAGCC[G/T]GAGCAATGTAGCAAG | 27342 |
| rs766934480 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786547 | TAGCTGGGACTAGTG[A/G]CACACACCACCATGT | 27342 |
| rs766935228 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715079 | TTTCCTTCTCTTTCT[C/G]TTTCTCCTCCTTCTC | 27342 |
| rs766953985 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717915 | ATGCACATTCTGTTA[C/T]TGAACTCATTGAGTT | 27342 |
| rs766999996 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711090 | CTTGAGCCCAGGAAG[-/T]TTGAGGCTGCAGTGA | 27342 |
| rs767007522 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712913 | TTGACCTCCCAGGTT[C/T]AAGTCATCCTCCCAC | 27342 |
| rs767016527 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700883 | GCTGGCCCTGTCCAG[A/T]CTCTCATACTGTGGG | 27342 |
| rs767019321 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700306 | TCCTTAAAAGTCCAT[C/T]GGCCTGAGCTCCTCT | 27342 |
| rs767020730 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686677 | TTTATTTGTTTGATG[-/T]TTGGATAAAGCTCCT | 27342 |
| rs767046021 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730061 | CAGCTGTGCCATAGA[C/T]TCAGGGTGGCCTCCA | 27342 |
| rs767057158 | snp | G/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739322 | AAGAATCTGAGAAAC[G/T]AATCAGTTAATCCCT | 27342 |
| rs767057265 | snp | A/G | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754541 | GTGAGCCCAGGAGTT[A/G]GAGACCAGCCTGGCC | 27342 |
| rs767078525 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798580 | CAGGGTAGTTGGAGT[A/G]CAGTTAGGGTGGGAC | 27342 |
| rs767094176 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810686 | AGTGACATCCACAGA[C/T]TATGCAGCTATACTT | 27342 |
| rs767120366 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804588 | AAAAATACAAAAAGT[A/T]GCTGGGTGTGGTGGC | 27342 |
| rs767139134 | in-del | -/TT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807214 | TTTGTGCCTTCTCTC[-/TT]TGTCCTCTTCTTGCC | 27342 |
| rs767142410 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762698 | CAGGTGGTAAGAACA[C/T]GCCTCTACCCTCTCC | 27342 |
| rs767159652 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783247 | AAATGGGATTTGGAA[A/C]GGTTGTCTGACATTT | 27342 |
| rs767164922 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748480 | GAATCACGGAACCAT[A/C]TGTTTTAACAGGCAT | 27342 |
| rs767176095 | snp | C/T | 1.64876e-05 | 0.00287116 | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66809026 | TGATGCTTGCTTAGG[C/T]GTCAAGCAAATGTAT | 27342 |
| rs767189832 | in-del | -/TC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732742 | CTCTCTCTCTTGCTG[-/TC]TCTCTCGCTCTCTTG | 27342 |
| rs767211702 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716523 | TGAGGATCGCTTGAA[C/T]CTGGGAGGCAGAGGT | 27342 |
| rs767253159 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770880 | TGATTAGTGATGTTG[A/C]GCATTTTTCACATTT | 27342 |
| rs767260900 | snp | C/T | 1.65913e-05 | 0.00288017 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797543 | CTTTGTAGTTACTAC[C/T]TTCTAATGGAAGAAC | 27342 |
| rs767261945 | snp | A/G | 3.29625e-05 | 0.00405958 | missense | RABGEF1 | GRCh38.p7 | 7:66809118 | AGAAACTGGAAAAAG[A/G]CCTCATAGATTGGAC | 27342 |
| rs767264162 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772576 | TATTTAAAAATTAGG[C/T]TAGCATTTGGTATTA | 27342 |
| rs767280467 | snp | C/T | 1.64743e-05 | 0.00287 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795503 | GCCTCTTTGTCTCTC[C/T]GTTTCAGGATCTAAG | 27342 |
| rs767297829 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731008 | ACAGCGCAGGGATTC[A/G]GGGCCAGGCTGCGGG | 27342 |
| rs767316424 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792655 | AATCCTTGAAAAGAT[A/G]TTGCAAAACAAAGGC | 27342 |
| rs767319057 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709547 | TAATCCCAGCACTTT[C/G]TGAGTCCGAGGTGGG | 27342 |
| rs767458330 | snp | A/G | | | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760624 | AATTTTTGTATTTTT[A/G]ATAGAGATGGAGTTT | 27342 |
| rs767466612 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779070 | CAGTGAGCTGAGATC[A/G]TGCCACTCCAGCCTG | 27342 |
| rs767479722 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698873 | TCCTCATCTGGAAAA[C/T]GGGGACAGGGACACC | 27342 |
| rs767483025 | snp | A/G | 1.65326e-05 | 0.00287507 | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66799353 | TACGCCTCAGATGCT[A/G]TGTGTCCCTGTTAAT | 27342 |
| rs767487446 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749594 | CCGGAGGTCAGGTAT[C/T]AGAGGCTGCAGTGCA | 27342 |
| rs767499442 | snp | A/G | 9.10523e-05 | 0.00674669 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772118 | TTGAACAGTGACGTG[A/G]CTGGATACATAGTTC | 27342 |
| rs767541292 | snp | G/T | 1.78739e-05 | 0.00298942 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783641 | CATGGATCTTTTATG[G/T]CATGAAACTTACTAT | 27342 |
| rs767568067 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715128 | TCCTCCTCTTCCTTT[C/G]TTCTTTCTTCTTCTC | 27342 |
| rs767603168 | in-del | -/AAAC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749976 | GAGACTCCATCTCAA[-/AAAC]AAACAAACAAAACTA | 27342 |
| rs767656600 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776864 | TATTTATTAGGAGGT[A/G]GAATAGCCAGGTAGT | 27342 |
| rs767687812 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735653 | TGAGTTATTGTGAGA[C/T]CTGGTGGTTTAAAAT | 27342 |
| rs767692368 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800529 | ATACTATTGTTTTTT[C/T]TTCTTGCAAGCTTTT | 27342 |
| rs767751190 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801617 | TTTAGCTCCCACCAA[G/T]GAGTGAGAACATGTG | 27342 |
| rs767785903 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788566 | CATGGCAATCAATTC[A/G]GTTTCTAAAAGACTT | 27342 |
| rs767790701 | in-del | -/TTTTTTTTTTTTT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806641 | AGTACTCATATATCC[-/TTTTTTTTTTTTT]TTTTTTTTGAGATGG | 27342 |
| rs767799264 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775482 | TCAGCTTTGTAATTT[C/T]TGTCAACTTTTTGAG | 27342 |
| rs767808432 | snp | G/T | 1.68026e-05 | 0.00289845 | splice-acceptor-variant | RABGEF1 | GRCh38.p7 | 7:66797373 | TGTCTGGTTATTTCA[G/T]TGCCTCCAGAAAGAG | 27342 |
| rs767815406 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742024 | GGCATCGTGGCGGGC[A/C]CCTGTAGTCCCAGCT | 27342 |
| rs767818133 | snp | C/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755154 | AAAAAATTAGCTGGG[C/T]GTGGTGGCAGGTGCC | 27342 |
| rs767843799 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702500 | CTTGGGTATATATCT[A/G]GGAGTGGAAATACTG | 27342 |
| rs767890570 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693073 | CCGTGGCCTTCACTC[A/G]GCTGAAAGGCACGTC | 27342 |
| rs767903582 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720400 | ACGGGGTTTCGCCAT[G/T]TTGGCCAGGCTGGTC | 27342 |
| rs767947359 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745442 | ATAGAAATGGTACCA[A/T]GTGAGTGGCTTCTTA | 27342 |
| rs767951315 | snp | A/G | 3.76506e-05 | 0.00433865 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771837 | GGTAAGATTTTATTT[A/G]GTAGAATGATAATTC | 27342 |
| rs767988255 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688469 | ATACACATTCTTTTC[A/C]AGAGCATGTGGGACA | 27342 |
| rs767995554 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762976 | GTAAGTGGGAAGGAT[A/G]GCAGTTTAAAACACT | 27342 |
| rs767995746 | snp | C/T | 0.000263591 | 0.0114772 | missense | RABGEF1 | GRCh38.p7 | 7:66805335 | ATATCCAGTATATCA[C/T]GCGCTTCTGCAATCC | 27342 |
| rs768009680 | snp | A/G | | | intron-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758354 | AAACCTAGCGCCGAG[A/G]CACAATTTACAGAAT | 27342 |
| rs768012144 | snp | A/T | 1.65154e-05 | 0.00287358 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66775371 | ATTCTTCAGTGCATC[A/T]TCCAGGGTCGGATCA | 27342 |
| rs768039223 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743736 | TCAATCTCCTGACCT[C/T]GTGATCCGCCCTCCT | 27342 |
| rs768113296 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732187 | CACACCAGTGGGCCT[C/T]GGTGCCTGGAGCACC | 27342 |
| rs768114168 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743236 | TGCTTGAACCTAGCA[A/G]TTCTAGGAGGTTGTG | 27342 |
| rs768150860 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734188 | AGGACAGCCATGCCC[C/G]AAACCACAGAGTCCG | 27342 |
| rs768173379 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800949 | GATAGGAGAGGCTGC[C/T]CGTTAAGTTACACAG | 27342 |
| rs768183208 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775025 | GCAGTAGCTGAATGA[A/G]TATGAGAAGACCCCA | 27342 |
| rs768215007 | snp | C/T | 1.67784e-05 | 0.00289636 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775418 | TGATACTCTTTTTTT[C/T]CTTCTCTGCCTGAGT | 27342 |
| rs768260254 | snp | A/G | | | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757131 | TTTGGAATGTTTGAC[A/G]CTGTTACAACATTTA | 27342 |
| rs768370883 | snp | A/G | 0.000228273 | 0.010681 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797331 | AAAAAAGAGAGAGAA[A/G]AAATATATATATCTT | 27342 |
| rs768440093 | snp | C/G | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681164 | AGCTGGGATTCCAAC[C/G]CAGGTCTATCTAAGA | 27342 |
| rs768444191 | in-del | -/TTAT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801891 | ACAACATCTGGAGAC[-/TTAT]TTATTTATTTAGTTA | 27342 |
| rs768450031 | in-del | -/AGAG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796143 | CTCTGTCTTCAAAAA[-/AGAG]AGAGAGAAAGAGAAA | 27342 |
| rs768452901 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797147 | TCCACAGAAAAAACC[C/T]ACAAAAATTATTCAG | 27342 |
| rs768470910 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710986 | TGTCACTACAAAAAA[A/C]AAATAATAAAGGAAA | 27342 |
| rs768506885 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808609 | TATATCCTGGGTGGG[A/G]ATAGCAGGTCTGGGA | 27342 |
| rs768523189 | snp | A/G | 1.66582e-05 | 0.00288597 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805119 | TTTCTCCTGGGAAAT[A/G]TTGTCTTTTCTGCTT | 27342 |
| rs768538831 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66809586 | CTGTGGTTTTGGTAA[A/G]TAATTGCCTTTTAAA | 27342 |
| rs768562302 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715872 | GCTCCTTGTGCCTCC[A/G]CCTCCTGAATAGCTG | 27342 |
| rs768567719 | snp | A/G | 1.64904e-05 | 0.00287139 | missense | RABGEF1 | GRCh38.p7 | 7:66809160 | CAAGAGAAGTTCAAG[A/G]CATCGTTGAGAAATA | 27342 |
| rs768603289 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722145 | CTGGGCAACAGAATA[A/G]GACCCTGTCTCAGGG | 27342 |
| rs768605306 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733087 | AGTCCTGGCCCCTAA[A/G]GCATTGGTGCTCTCT | 27342 |
| rs768615266 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762538 | CGAGTGTTGTGAGCC[A/G]TGATCACACCACTGC | 27342 |
| rs768625825 | snp | A/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754225 | GCCAGGACAGTCTCG[A/T]TCTCCTGACCTCATG | 27342 |
| rs768645343 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783608 | AACCTTAGGTAAGAT[A/T]CTTAAAGTAATTCCA | 27342 |
| rs768668558 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770588 | TCCTGGGCTCAGGCA[A/G]TCCTTCTGTCTCAGC | 27342 |
| rs768684424 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66805249 | CAAGAATGAGCCGGC[A/G]TCAGCGGATGACTTC | 27342 |
| rs768707635 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703861 | GATAGGGATTGCACT[A/G]AATCTGTAGATCATT | 27342 |
| rs768721141 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752612 | TAAATGGACATTTTC[A/G]TAATTGTGGTGTTTT | 27342 |
| rs768728920 | snp | A/T | 4.94222e-05 | 0.00497078 | missense | RABGEF1 | GRCh38.p7 | 7:66795574 | AATGTGGCCGAAAGG[A/T]TGCAAACTCGTGGGA | 27342 |
| rs768732708 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699853 | GAGAGACCCTGTCTC[A/T]AAAATAAAATAAAAA | 27342 |
| rs768742841 | snp | C/T | 1.64817e-05 | 0.00287064 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795462 | AATGTAGAGCTGTGC[C/T]TCTGCACTTTGTTCA | 27342 |
| rs768744267 | in-del | -/TG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701091 | GGCAGGGGTGGGGAC[-/TG]TGTTTGTGAGCAGCC | 27342 |
| rs768750782 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740184 | TGCTCTGTGGCCCAG[C/G]CTGGTCTCGAACTCC | 27342 |
| rs768752513 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782540 | GTGGGATGATCTCGT[A/T]GCTCACTGCAGCGTC | 27342 |
| rs768793272 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718958 | CTGCCACATACTTCT[C/T]ACGACTGCATCTTTC | 27342 |
| rs768805272 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688760 | GGATGCAGTTAAAGC[A/C]GTGCTCAGAGGGAAA | 27342 |
| rs768831349 | in-del | -/AT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797334 | AAAGAGAGAGAAAAA[-/AT]ATATATATCTTGATC | 27342 |
| rs768848832 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749116 | ACCTCACCTCCATAC[-/A]GAGATGGGCTGAGGG | 27342 |
| rs768861868 | snp | C/G | 1.76042e-05 | 0.00296678 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772088 | GGAGCGGTAAAAGGA[C/G]TTAACTAGGGGCGGT | 27342 |
| rs768898949 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689606 | TCAGGAGTTAGAGAC[C/T]AGCCTGGCCAACATG | 27342 |
| rs768904156 | in-del | -/TTTG | 0.00095914 | 0.0218781 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773662 | ATAGTGCTTGTGCTT[-/TTTG]TTTGTTTGTTTGTTT | 27342 |
| rs768913367 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66753855 | GGGACTACAGGCATG[C/T]GCCATCATGCCTGGC | 27342 |
| rs768953902 | snp | C/T | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759908 | TTTAAAACTGATCAC[C/T]GTTACAGCAACTCCA | 27342 |
| rs768973282 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708236 | TGTGTTTGCCCTGGG[A/T]TAACAATTAACATCT | 27342 |
| rs769037158 | in-del | -/CT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692749 | ATGTCCTACATCCCC[-/CT]GAGCCTAGGATGGGA | 27342 |
| rs769050569 | snp | C/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739481 | CAACATGGTGAAACC[C/T]TGTCTCGACTAAAAA | 27342 |
| rs769079225 | in-del | -/AAAAAAC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788447 | AGACTCCATCTCAAA[-/AAAAAAC]AAAAAACAAAACAAA | 27342 |
| rs769116881 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695299 | CCTGAGCAGCAGAGC[A/G]AGACCCTGTCTCAAA | 27342 |
| rs769169692 | in-del | -/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708477 | ATTTTTAGTAGAGAC[-/G]GGGTTTCACCATGTT | 27342 |
| rs769189994 | in-del | -/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764391 | AAATGACTTGCAAAT[-/G]GTTTTCTCTTATTCT | 27342 |
| rs769194689 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778286 | TAGCAGCTTGGTAGC[A/T]GACAAAATACAAATA | 27342 |
| rs769214482 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807022 | TTCTTTATCCAAAGC[A/G]AGTCAGACAACCTGG | 27342 |
| rs769221072 | snp | C/T | 4.94613e-05 | 0.00497275 | missense | RABGEF1 | GRCh38.p7 | 7:66809091 | GACAAGAAAGGATCA[C/T]GAATGAAGCCAAGAA | 27342 |
| rs769221108 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748820 | TTTTCCATTTCTCCA[A/G]TTCGAACTTTCTGAT | 27342 |
| rs769232991 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775908 | GGGGATGAAAGTGAG[C/T]CATAGTAGCTATTTT | 27342 |
| rs769239112 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791885 | TTAGGAGGCCGAGGA[A/G]GATGGATCACGAGGT | 27342 |
| rs769281449 | in-del | -/TTGTGTGTGT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702347 | TGGCTATTGTTTTGT[-/TTGTGTGTGT]GTGTGTGTGTGTGTG | 27342 |
| rs769293957 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714012 | TTCATAGAGACTATT[G/T]GTCTGTGTAGACTTC | 27342 |
| rs769363685 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723642 | CTTGAGTGTAGTGGT[A/G]TGATCTTGGCTCACC | 27342 |
| rs769429236 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777054 | GAGCTTAGCACAGTG[C/T]CTGACACACACAGTA | 27342 |
| rs769435820 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693748 | GACTACGACCCTCAG[A/G]GAATCATTCATTCAT | 27342 |
| rs769447612 | snp | C/T | 1.6821e-05 | 0.00290004 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799320 | CTGTCTCTCTCTCTT[C/T]AGAGCCCTGCGCTGG | 27342 |
| rs769453926 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771340 | GAGACAGGGTTTCAC[C/T]GTGTTAGCCAGGATA | 27342 |
| rs769465100 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700406 | AGGTCTCCCCGGAAA[C/G]TGTTTGACTCCAGGT | 27342 |
| rs769475687 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694204 | GAGGTCCCAATGCAG[C/T]GGGGGACACCGTGGG | 27342 |
| rs769485718 | snp | C/T | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759159 | CTTATGACTCTGTAG[C/T]CACATCCTGTGTCAG | 27342 |
| rs769505175 | in-del | -/GC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690377 | GTGCTGGGATTACAG[-/GC]GTGAGCCATCGCGCC | 27342 |
| rs769521395 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732799 | TCTTGCTGTCTCTCT[C/T]GCTTTTGCTCTCGCT | 27342 |
| rs769534172 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700176 | TTCCAGCCCTGGTTC[A/C]TTCTGGATCCAAGCA | 27342 |
| rs769543780 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713386 | GCCCGCCTTGGCCCT[C/T]CAAAGTGCTGGGATT | 27342 |
| rs769582358 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704734 | GAGAATGGTGTGAAC[C/T]CAGGAGGCGGAGTTT | 27342 |
| rs769592959 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699207 | CCCCTCTCCAGGGAG[A/G]GCTAGGGACCCATGT | 27342 |
| rs769619215 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771730 | CATTCTTTTTTCTTC[C/T]TTCCTCCTCTTTCTC | 27342 |
| rs769628886 | snp | C/G | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755076 | AAGGCAGGCGGATCA[C/G]GAGGTCAGGATATTG | 27342 |
| rs769630633 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703486 | GATACATGAGGTGGG[A/G]TAAAGGTCTAACTTT | 27342 |
| rs769671603 | snp | C/T | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759032 | AAACCAGGAAATTGA[C/T]ATTTGTGCAATGTAT | 27342 |
| rs769676685 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764265 | CACGACTGTTTGCAT[A/G]TCTTTCTGGAGAAAT | 27342 |
| rs769719328 | snp | C/T | 0.000952653 | 0.0218041 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796905 | CTGGTAAGTTTTTTT[C/T]TTAAGCGTATTTTTA | 27342 |
| rs769722299 | snp | C/G | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681450 | GCTCTGTCACCCGGG[C/G]TGGAGTTCAGTGGAG | 27342 |
| rs769730700 | snp | C/T | 1.74014e-05 | 0.00294965 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797358 | TCTTGATCTTTTCTC[C/T]GTCTGGTTATTTCAG | 27342 |
| rs769738293 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712491 | TTTTCTTTTTCTTGA[G/T]ACTGGCTCTCACTTT | 27342 |
| rs769742220 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725163 | ATATTTTCCCACTTC[C/T]TTACATGTCTGTACA | 27342 |
| rs769745426 | in-del | -/CT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732697 | AGCTGCGCTCTTGTG[-/CT]CTCTCTCTCTCGCTC | 27342 |
| rs769786680 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763679 | TCAGTGACCACTACT[C/T]TATTTTCTGTCTCTA | 27342 |
| rs769812558 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682984 | GCGCGAGTGACCAAT[C/T]CTTGTGGTTGGGAAA | 27342 |
| rs769813729 | snp | G/T | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760110 | TGACCAAGCAGGCCC[G/T]TCTGAGAATGTGCAT | 27342 |
| rs769822507 | snp | C/G | 1.69513e-05 | 0.00291125 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775438 | TCTGCCTGAGTGAGA[C/G]ACAGAGGAGATCCCC | 27342 |
| rs769838172 | snp | C/T | | | intron-variant, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66685588 | ATTTGTAAACAGGAA[C/T]TCTGCACTCATTTCT | 27342 |
| rs769861677 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773476 | TTTTAATTGTGACCC[A/T]GCTAAATCTCTCGGA | 27342 |
| rs769888649 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719799 | TTATTAAATTACATA[C/T]TGTCTTTTCCTGTTT | 27342 |
| rs769908229 | snp | A/T | 1.66208e-05 | 0.00288273 | intron-variant, missense | RABGEF1 | GRCh38.p7 | 7:66783719 | TCCATAAACCGGCAA[A/T]CCAGCATTGAAACGG | 27342 |
| rs769911029 | in-del | -/TGT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686600 | TTAAATAATCTAGAC[-/TGT]TGTTATAATACGTAA | 27342 |
| rs769911460 | snp | A/C | 1.6473e-05 | 0.00286988 | missense | RABGEF1 | GRCh38.p7 | 7:66805272 | ATGACTTCCTCCCCA[A/C]CCTCATCTACATTGT | 27342 |
| rs769911643 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690007 | TTTCTAACTCATTCT[A/G]TGAGGCCAGCATTGC | 27342 |
| rs769935493 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741528 | CGGTGTCTCAGCGCG[A/G]GTGACCAATCCTTGC | 27342 |
| rs769946661 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742846 | TCCTGCACTCAAGCA[A/G]TCTTCCTGCCTCAAG | 27342 |
| rs769981374 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798959 | CTCCATCTCAAAAAA[C/G]AAAGAAGTTGAGGAC | 27342 |
| rs770050881 | in-del | -/TA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720189 | TATTATTATTATTAT[-/TA]TATTATTTTTTTTTT | 27342 |
| rs770097920 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807377 | AGAGTCCTTTGTTCT[G/T]CAACTTCTGTTGTTC | 27342 |
| rs770117410 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805416 | GTAAGTGAGTTCTTG[A/G]TGTTGTGGAGAAGGA | 27342 |
| rs770155792 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707209 | TTTTGAATTACTTCA[C/G]ATTTTAACAATTTAT | 27342 |
| rs770208876 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709330 | AATGCATCTGTAATT[A/G]TTTTTTAAACTGCAA | 27342 |
| rs770257583 | snp | C/T | | | utr-variant-3-prime | RABGEF1 | GRCh38.p7 | 7:66809364 | GATTGGGATCTAGAA[C/T]GTAACTAAATTGCTT | 27342 |
| rs770314194 | in-del | -/CCCGCCTCGAC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66757855 | TGACCTCGTGATCCG[-/CCCGCCTCGAC]CTCCCAAAGTGCTGG | 27342 |
| rs770316421 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778336 | GAATATCTTCACATT[C/G]TTTTAGAGTTGGATA | 27342 |
| rs770321481 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725368 | CACAGTCCCTCCATT[C/T]TGCCCCACCCTCAGC | 27342 |
| rs770341293 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784520 | ATAGGGATTAATTCT[C/G]TTGTAACATTCTATA | 27342 |
| rs770346275 | snp | G/T | 3.29484e-05 | 0.00405871 | missense | RABGEF1 | GRCh38.p7 | 7:66795586 | AGGATGCAAACTCGT[G/T]GGAAAGGTAACACTG | 27342 |
| rs770375845 | snp | A/G | 1.66266e-05 | 0.00288323 | missense | RABGEF1 | GRCh38.p7 | 7:66799331 | TCTTTAGAGCCCTGC[A/G]CTGGGTTACGCCTCA | 27342 |
| rs770376207 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764528 | TAAACATCCTTTGTC[A/C]AATCCAATATCATGA | 27342 |
| rs770380444 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749877 | TACTCGGGAGGCTGA[A/G]GCAGGAGAATCGCTG | 27342 |
| rs770416502 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767472 | CTTTATAGTCACATT[A/C]TTTCCTACCCCTAGT | 27342 |
| rs770520666 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66682583 | CCCCTCGGTCCGGCT[C/G]CCACTTCCCCGTCCA | 27342 |
| rs770536905 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734463 | CAATGATTTGTATTT[C/T]TGTATTTTTTTTAGT | 27342 |
| rs770537452 | snp | A/G | 3.58076e-05 | 0.00423114 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772101 | GACTTAACTAGGGGC[A/G]GTTGAACAGTGACGT | 27342 |
| rs770537510 | snp | C/T | 3.32474e-05 | 0.00407708 | missense | RABGEF1 | GRCh38.p7 | 7:66799406 | ATATGGTGGTGAAGG[C/T]GATCACAGGTCAGTG | 27342 |
| rs770538701 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726686 | AAGCAGAGGTTTTGT[C/T]TTCAGGATAATGAAA | 27342 |
| rs770555767 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774176 | AGCTACAACTTGACC[-/A]AGTTCTATTTCTTCC | 27342 |
| rs770599497 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683118 | AGAGCTACTTTCCCC[-/T]CTCTAAATCTAAAAC | 27342 |
| rs770618150 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694319 | TGACTTGGCAAGGTG[A/G]TTTGTGGAATAGTGA | 27342 |
| rs770626833 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733653 | CAGTGAGCCAAGATC[A/G]TGCCACTGCACTCCA | 27342 |
| rs770642939 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723959 | TTTTTAGTGCTTTTC[A/G]TTGTCTTGTATTTCA | 27342 |
| rs770688305 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798524 | CCCTGGACCAAGATG[C/G]AGAACAGAAGCAGTA | 27342 |
| rs770722585 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741669 | TGGAGAGCTGCTTTC[C/T]CCCCTCTAAACCTAG | 27342 |
| rs770759908 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730614 | CCCAGGCTGGAGTGC[C/T]ATGGTACAGTCTCGG | 27342 |
| rs770792639 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786162 | TTTTCTCCAAGCCCT[C/G]TATATGCCGGTGGTG | 27342 |
| rs770806853 | in-del | -/TTCTC | 1.84691e-05 | 0.00303878 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797353 | ATATATCTTGATCTT[-/TTCTC]TGTCTGGTTATTTCA | 27342 |
| rs770810505 | snp | A/G | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755276 | TCCAGCCTGGGCAAC[A/G]GAGTGAGACTCTGTC | 27342 |
| rs770818373 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66685195 | GAGTCTTGCTCTGTC[A/G]CTGGGCTAGAGTGCA | 27342 |
| rs770867651 | in-del | -/TAT | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681282 | AGCTACTGTTTTTAA[-/TAT]TCCTTACATGGGAAT | 27342 |
| rs770876580 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735595 | GTGACAGGATCATTG[-/T]TGGGGGGGGTTTCCC | 27342 |
| rs770880407 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799857 | TAAAATGATGCCTCT[A/G]ACTGGTTGTTAGAGA | 27342 |
| rs770914431 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714404 | TTGTAGAATTTGTAG[C/T]GATATCACGTATTTC | 27342 |
| rs770933748 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765799 | GATCCTGAATTGGGG[A/G]ACCATTCACCTTATA | 27342 |
| rs770965008 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761260 | ATCACACAGGGTGAG[A/G]ACTCAGTCCCCATGA | 27342 |
| rs770979882 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794842 | TGGTAGAGGAGAGTC[A/G]AAGAAGTCAGTTAAT | 27342 |
| rs771010556 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690205 | CTCCCAGGTTCAACC[A/C]GTTCTCTGCCTCAGC | 27342 |
| rs771050809 | snp | A/G | 3.42577e-05 | 0.00413856 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808835 | TTTACAAATCGACTC[A/G]AGTATGCATAGCTTT | 27342 |
| rs771064295 | snp | A/G | 1.76076e-05 | 0.00296707 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66771894 | TCAGTGGTTAGCAGG[A/G]AGAAGATGAGCCTTA | 27342 |
| rs771069748 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722267 | CAACATGGTGAAACC[C/T]CACCTTTACTAAAAA | 27342 |
| rs771098706 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696416 | ACCGTGGGGCTGGGC[G/T]TGGTGGCTCACGCCT | 27342 |
| rs771152517 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735554 | CAAATTGTAATCCCT[A/G]AAGTTGGAGGTGAGG | 27342 |
| rs771152566 | snp | A/G | 4.9436e-05 | 0.00497148 | missense | RABGEF1 | GRCh38.p7 | 7:66808959 | AGGATTTTGATCGCT[A/G]CATGTCTGGCCAGAC | 27342 |
| rs771153425 | snp | C/T | 3.43212e-05 | 0.00414239 | missense | RABGEF1 | GRCh38.p7 | 7:66809273 | CTGCAACCTCAAGTT[C/T]ATGCAGGATGATCAC | 27342 |
| rs771153727 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726100 | AGGAAGCTGCTACTC[-/A]AGACAGGGCCAGAAG | 27342 |
| rs771154167 | in-del | -/TATT | | | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756840 | CAGTTATTGCAACAC[-/TATT]TATTGAAAATTTCCC | 27342 |
| rs771188932 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710317 | TGTTTTTTAGCGTTT[A/G]GCTTTTACCAGTAAA | 27342 |
| rs771209308 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719914 | AAGGTTTGCTGGTCC[C/G]TGATGTGGACCAGCA | 27342 |
| rs771228125 | in-del | -/TTA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784851 | AAAACAAGTGAGCTG[-/TTA]TTGTTTTTTTTTTAA | 27342 |
| rs771292167 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687856 | TCTGGGAGGCTGAGG[C/T]GGGCAGATCCCTTGA | 27342 |
| rs771297089 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721009 | TGCAACCTCCACTTC[C/T]CAGGTTCAAGTGATT | 27342 |
| rs771300815 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728191 | GAATTGGGAGGGCCT[A/G]TCCCTAAGCACTGGC | 27342 |
| rs771322620 | in-del | -/TTT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66743326 | AAAAAAAGAAAAAAA[-/TTT]AAAAAAAAAAAAAAG | 27342 |
| rs771347100 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736535 | ACTGAAGGCTTGAGC[C/T]CTAGAGCAGTGATAA | 27342 |
| rs771367819 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727759 | AGTGGCAGGCTGCCC[A/G]TGGATAATGGAAAAG | 27342 |
| rs771372165 | in-del | -/TTAT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799884 | GAGAAGCGCTATGAG[-/TTAT]TTTTCTGGTTTGATC | 27342 |
| rs771390783 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717334 | CCCTGTCCTTACTAT[A/G]TTGTAGTTATCATAT | 27342 |
| rs771410123 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788578 | TTCAGTTTCTAAAAG[A/T]CTTCTTAATAGTCAT | 27342 |
| rs771420759 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752262 | GCTTTGGGAGTCCGA[G/T]GTGGACGGATCACAA | 27342 |
| rs771437501 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767326 | TTTTTTGTTTAAATC[A/G]TAGAGTAAAATTGAT | 27342 |
| rs771499102 | in-del | -/CGGAAGC | | | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740443 | CCAGCTGTTGCGCGT[-/CGGAAGC]CGGAAGCCGGAAGCA | 27342 |
| rs771536596 | snp | A/G | 0.00133958 | 0.0258456 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796929 | ATTTTTAAATATAAC[A/G]TTCTTATACTTTTGT | 27342 |
| rs771574875 | snp | A/G | 3.29462e-05 | 0.00405857 | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66805246 | CACCAAGAATGAGCC[A/G]GCGTCAGCGGATGAC | 27342 |
| rs771654364 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766197 | AACAACAATTAGCCA[C/G]GCATGGTGGCTGAGT | 27342 |
| rs771686885 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800046 | AAAAAAAAATCTTAA[C/T]GGAGAGATGGTCATC | 27342 |
| rs771717095 | snp | A/G | | | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756896 | TAAATTACCTTATAT[A/G]TTACATTAGATTCAT | 27342 |
| rs771732091 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800834 | TTCACTGGGCGACAG[C/G]TGGTAGCGAGTGTTT | 27342 |
| rs771736399 | snp | A/G | 3.30158e-05 | 0.00406286 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66775322 | AAGAAAAGAAAACCA[A/G]CGAGAAGACCCGCAA | 27342 |
| rs771756793 | snp | A/G | 1.64947e-05 | 0.00287177 | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66809173 | AGACATCGTTGAGAA[A/G]TACCCACTGGAAATT | 27342 |
| rs771783769 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725795 | GTCTGAGGGAAGACA[C/T]AAGGAGCTCCCCCGA | 27342 |
| rs771826846 | snp | A/C | | | intron-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811795 | TGCTACTTATTAGCT[A/C]ATTGGCCCTGAACAA | 27342 |
| rs771873937 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726719 | GTCTAAAATGGACTG[C/T]GAGGTCAGGTGCGGT | 27342 |
| rs771879093 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721150 | TCTCGAACTCCCGAG[A/C]TCAAGTGATCTGCCG | 27342 |
| rs771914903 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742803 | GTAAAGATGTTGTCT[G/T]GCTGTGTTGCCCTGG | 27342 |
| rs771919665 | snp | A/G | 5.32912e-05 | 0.00516166 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799447 | CCTTTTTATTGGGAT[A/G]TTTTCCCCTTAAAGT | 27342 |
| rs771930641 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787947 | CATGTTTAGACTGCA[A/G]TTAAATAAAAGTAAA | 27342 |
| rs772024929 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773756 | CTGCAACCTCTGCTT[C/T]CTGGGCTCAAGTGAT | 27342 |
| rs772055197 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703032 | AGGCTGGAGGGCAGT[A/G]GTGCTATCTCAACTT | 27342 |
| rs772064524 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807009 | GTTTTGGATTCAGTT[A/C]TTTATCCAAAGCGAG | 27342 |
| rs772094931 | snp | C/T | 1.648e-05 | 0.0028705 | missense | RABGEF1 | GRCh38.p7 | 7:66808977 | TGTCTGGCCAGACCT[C/T]TCCCAGGAAGCAAGA | 27342 |
| rs772131439 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762134 | GCCAGGGACTGTGGA[C/T]GAAAACCAATATATA | 27342 |
| rs772132665 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787366 | TTTTTTTTTTAAGAT[-/A]AGAGTCTTGCTCTGT | 27342 |
| rs772135630 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725359 | CCCTTGTCCCACAGT[C/T]CCTCCATTCTGCCCC | 27342 |
| rs772139153 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804551 | ACCAGCCTGGCCAAC[A/T]TGGTGAAACCCCGTT | 27342 |
| rs772144712 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703363 | TCTAGAAAATCATTG[C/T]CAAATCCCAGGTCTT | 27342 |
| rs772170768 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796061 | AGAATTGCTTGAACC[C/T]GGAAGGCGGAGGTTG | 27342 |
| rs772172823 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720202 | TATTATTATTTTTTT[A/T]TTTTTTTCTTTGAGA | 27342 |
| rs772247256 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686580 | TTCACATGGCTGAAG[A/T]GAGTTTAAATAATCT | 27342 |
| rs772254366 | snp | A/G | 1.66493e-05 | 0.0028852 | intron-variant, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66783733 | AACCAGCATTGAAAC[A/G]GATAGAGTGTCTAAG | 27342 |
| rs772254607 | snp | A/G | 0.00051115 | 0.0159785 | missense | RABGEF1 | GRCh38.p7 | 7:66809072 | TTGTCTCAGTTGAAT[A/G]AACGACAAGAAAGGA | 27342 |
| rs772266849 | snp | C/T | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680926 | TCTCGACTAAAAATA[C/T]GAAAAAATTAGCTGG | 27342 |
| rs772268583 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782296 | TCTAGTTTGTCTCTT[A/G]CCCATCTAGTTCCTA | 27342 |
| rs772277331 | snp | G/T | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759248 | TTATTCCTTGCTATG[G/T]TTTGTTACAGTGAGG | 27342 |
| rs772285729 | snp | C/T | 1.65255e-05 | 0.00287445 | missense | RABGEF1 | GRCh38.p7 | 7:66797430 | AAGTACATCATGACT[C/T]GTCTCTATAAATATG | 27342 |
| rs772331527 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698899 | ACACCTACAGCAGGG[A/G]GTTCCATGGTGTGCT | 27342 |
| rs772333062 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769244 | TCAGAATCCTCAAAA[A/G]TAGTGCACAGTGCAT | 27342 |
| rs772353800 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738141 | TCCTATCACCTCGGC[C/T]TCCAGAGTAGCTGGG | 27342 |
| rs772392964 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718728 | CTGGAACCTGGGGAG[C/T]GGTCCATCCTGTAAT | 27342 |
| rs772427168 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764481 | AGTACAATTTATCTG[C/T]CTTTTGTTGCTCCTG | 27342 |
| rs772428123 | in-del | -/TGTTTGTGTGTGTGTG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702344 | TTCTGGCTATTGTTT[-/TGTTTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 27342 |
| rs772434615 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710805 | ATATGTTCTTTAAAG[A/G]TTTTCTTTCTTGGGG | 27342 |
| rs772450451 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688290 | AAGCAAGAAAGGGTA[C/G]AATTGAAGGGAAAAG | 27342 |
| rs772500516 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728278 | AGCTAAGCTTGGGGG[C/G]GCCACTGGGTCCCCT | 27342 |
| rs772550853 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711672 | GCTCGCTGCAAGCTC[C/T]GCCTCCTGGGTTCAA | 27342 |
| rs772596726 | snp | C/G | | | missense | RABGEF1 | GRCh38.p7 | 7:66805144 | CTGCTTTGTAGATAT[C/G]ATTGAAATGGATTCC | 27342 |
| rs772607012 | in-del | -/AG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66685314 | CTCGCCACCATGCCC[-/AG]AGCTAATTACTTCTG | 27342 |
| rs772618956 | snp | A/C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792005 | TAGTCCCAGCTACTC[A/C/G]GGAGGCTGAGGCAGG | 27342 |
| rs772674683 | in-del | -/TTTG | 0.00095914 | 0.0218781 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773663 | ATAGTGCTTGTGCTT[-/TTTG]TTTGTTTGTTTGTTT | 27342 |
| rs772674778 | snp | C/T | 3.3248e-05 | 0.00407712 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66771943 | TTCATGTGGATCAAT[C/T]GGATCTCCTGTGCAA | 27342 |
| rs772683503 | snp | A/G | 3.37593e-05 | 0.00410834 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66771922 | TTAAGTCTGAACGCC[A/G]AGGAATTCATGTGGA | 27342 |
| rs772707737 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764290 | AGAAATGTCCATTCA[A/G]ATCTTTTACCTGCTA | 27342 |
| rs772711926 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732800 | CTTGCTGTCTCTCTC[A/G]CTTTTGCTCTCGCTC | 27342 |
| rs772712499 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746108 | TATTGTTACAATATG[C/T]AAACATGTGAAATAA | 27342 |
| rs772743552 | in-del | -/CCTGTTC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728462 | TTGCCTCTGCTTGTT[-/CCTGTTC]CCACCATAACCATGA | 27342 |
| rs772766479 | snp | A/G | 1.65097e-05 | 0.00287308 | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66797474 | AACTACTGATGATGA[A/G]AAGAAAGATCTTGCC | 27342 |
| rs772771696 | snp | C/T | 1.74385e-05 | 0.00295278 | utr-variant-5-prime, stop-gained | RABGEF1 | GRCh38.p7 | 7:66772077 | TGGGAGCTGGCGGAG[C/T]GGTAAAAGGACTTAA | 27342 |
| rs772788495 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723643 | TTGAGTGTAGTGGTG[A/T]GATCTTGGCTCACCA | 27342 |
| rs772818987 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769794 | ACTCTGTAGCTTAGA[C/G]TTTTAAAAAGCCATC | 27342 |
| rs772836836 | snp | C/T | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66681339 | CAATTTGTGACTCAA[C/T]CATTCATACTTTGTG | 27342 |
| rs772840366 | in-del | -/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702324 | ATATTTGGGTGGCTT[-/C]CACCTTCTGGCTATT | 27342 |
| rs772860778 | snp | G/T | 1.66507e-05 | 0.00288532 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805442 | AAGGACTAGGAAGGT[G/T]GTGGTTTTGGGGATG | 27342 |
| rs772879237 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688882 | AGGATCACCTGAGGT[C/T]AGGAGTTCAAGACCA | 27342 |
| rs772885164 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807600 | ACACTTGTATTGCAC[C/G]TCAAATATAATTTGT | 27342 |
| rs772888664 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752790 | TGATATTGATGTACA[A/T]TCAAGTCTGAGAAAC | 27342 |
| rs772901636 | snp | C/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754122 | ATTCTCCTGCCTCAC[C/T]TCCCGCGTAGCTGGG | 27342 |
| rs772922011 | snp | C/T | | | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757680 | GCAGTGGCATGATCT[C/T]GGCTCACTGCAAGCT | 27342 |
| rs773006337 | in-del | -/AATT | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680621 | TTTGAGAAACGAATC[-/AATT]AATCTCCACTTTACC | 27342 |
| rs773013474 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749787 | CCATCCTGGCTAACA[C/G]AGTTAAACCCCGTCT | 27342 |
| rs773018188 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734538 | TGACCTCAAGTGATC[C/T]GCCCATGTTGGCCTC | 27342 |
| rs773071122 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699275 | CTTCTTTTTCTGCCT[C/T]ATTCTCTGTTCCCCT | 27342 |
| rs773092217 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712578 | CGGGCTGAAGGGATC[C/T]TCGCACCTCAGCCTC | 27342 |
| rs773094696 | snp | A/G | 1.84869e-05 | 0.00304024 | utr-variant-3-prime | RABGEF1 | GRCh38.p7 | 7:66809327 | GAGCCTAAATTGTAG[A/G]TAGCCCTTACTACAC | 27342 |
| rs773139782 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798391 | GTCCCAGGTTCCAGA[C/G]AAGGGGCTGGTACTT | 27342 |
| rs773143325 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714069 | TTGATGTAAAGGTAA[C/T]GTTGGCTTTATACAA | 27342 |
| rs773162315 | snp | G/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66738658 | GATCACTTGAGCCAG[G/T]GAGTTGGAGGCTGGA | 27342 |
| rs773207189 | snp | A/G | 1.69384e-05 | 0.00291014 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775439 | CTGCCTGAGTGAGAC[A/G]CAGAGGAGATCCCCA | 27342 |
| rs773224725 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794375 | TGCCCAGGCTGGCCT[C/G]AAACTCCTAGGCTCA | 27342 |
| rs773330945 | in-del | -/TTAG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801899 | TGGAGACTTATTTAT[-/TTAG]TTAGTTAGTTAGTTA | 27342 |
| rs773399742 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749027 | TCAGGCTCACCGTGA[C/G]TTCCTCCACTGAAGC | 27342 |
| rs773418350 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707085 | CCACCGCGCCCGGCC[C/T]GTACTGGTTATTTTT | 27342 |
| rs773425435 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690018 | TTCTATGAGGCCAGC[A/G]TTGCATTGATAACTA | 27342 |
| rs773441926 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66805276 | CTTCCTCCCCACCCT[C/T]ATCTACATTGTTTTG | 27342 |
| rs773455868 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727755 | CGTGAGTGGCAGGCT[A/G]CCCGTGGATAATGGA | 27342 |
| rs773489658 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748091 | GGGTCAGTGACCATA[C/T]GACAAAAGAGATCAT | 27342 |
| rs773613694 | in-del | -/AAAAAAA | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739659 | AGAGTGAGAGTCTCA[-/AAAAAAA]AAAAAAAAAAAAAAA | 27342 |
| rs773648857 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801262 | TTTTTAATTTTTATG[C/T]GTACATAATAGGTGT | 27342 |
| rs773648980 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786484 | TTGCTGCTCACTGCA[A/G]ACTTGACCTCCCAGA | 27342 |
| rs773652871 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695566 | GGACTGGGGACAAAA[A/G]CCAGGCTGGAGAGAG | 27342 |
| rs773654662 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735372 | CTTTATAGCATAGTA[C/G]TTTAGATTATGGGCT | 27342 |
| rs773680020 | snp | A/G | 3.29647e-05 | 0.00405971 | missense | RABGEF1 | GRCh38.p7 | 7:66809105 | ATGAATGAAGCCAAG[A/G]AACTGGAAAAAGACC | 27342 |
| rs773720864 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714913 | GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC | 27342 |
| rs773736662 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800137 | GTTAATGAAATTCTA[C/T]TGGAAAGGAAGTGGG | 27342 |
| rs773750717 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707326 | GGGTAGGATGTTCTA[C/T]AGATGTTCGTTAGGT | 27342 |
| rs773769828 | snp | A/G | 1.64773e-05 | 0.00287026 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795485 | TTTGTTCAGCTACAA[A/G]CAGCCTCTTTGTCTC | 27342 |
| rs773784585 | snp | A/G | 1.64746e-05 | 0.00287002 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795595 | ACTCGTGGGAAAGGT[A/G]ACACTGTTAGCCATT | 27342 |
| rs773813527 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694361 | TTACAGGCAGCAGTG[A/G]TGGTCGGGAGAAGAT | 27342 |
| rs773815765 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810435 | GTCAGATGTCTCCTG[A/G]GGCCATATCACCCCT | 27342 |
| rs773824119 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66685692 | TCATTGATTTCTTTG[A/G]TTTTTGTTGCTGGTT | 27342 |
| rs773828504 | snp | C/T | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755801 | TTGTCTAGAACTCAT[C/T]CCTTGAGAATGCTCC | 27342 |
| rs773840147 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724004 | TTTTTCCTTTAGCCT[A/G]AAATTTTAATTTTAT | 27342 |
| rs773863321 | in-del | -/TT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732736 | CTCGCTCTCTCTCTC[-/TT]GCTGTCTCTCTCGCT | 27342 |
| rs773863461 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764546 | TCCAATATCATGAAA[A/G]TTTTACCTCTACATT | 27342 |
| rs773885514 | snp | C/T | 1.65723e-05 | 0.00287852 | missense | RABGEF1 | GRCh38.p7 | 7:66799340 | CCCTGCGCTGGGTTA[C/T]GCCTCAGATGCTGTG | 27342 |
| rs773911125 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767527 | TAAACTTTTAAGATG[A/G]CTGCTATGGTCTGAA | 27342 |
| rs773914620 | snp | A/G | 3.63689e-05 | 0.00426417 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772115 | CGGTTGAACAGTGAC[A/G]TGACTGGATACATAG | 27342 |
| rs773919307 | in-del | -/TG/TTG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738017 | TTGTGTTTTTTGTTT[-/TG/TTG]TTTTTGTTTTTTTTT | 27342 |
| rs773972545 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683730 | TACAAGGAGGTGCTT[A/G]TTTATTTATTTATTT | 27342 |
| rs773978855 | snp | A/C | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739248 | AGCCACTGCGCCTGG[A/C]CTTACTTTTGTTTTA | 27342 |
| rs774050942 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66766158 | CCTGGGTAACGTGGC[A/G]AAACACCGCCTCTAC | 27342 |
| rs774051050 | snp | A/G | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754194 | TTTTTAGTAGAGACG[A/G]GGTTTCACTATGTTA | 27342 |
| rs774089448 | in-del | -/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770567 | ACCTCACTGCAGCCT[-/C]CCAACTCCTGGGCTC | 27342 |
| rs774116278 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691246 | GTACACCTCCCATAC[C/T]GTACATAATTCTATA | 27342 |
| rs774129700 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764256 | TCATATACTCACGAC[-/T]GTTTGCATATCTTTC | 27342 |
| rs774134259 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716198 | TAAATTTCCTTGCTT[G/T]GAGGTATAGTTTGTC | 27342 |
| rs774188260 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794802 | TGCACAACAGTGAAA[A/G]AGGGGGAGCAACTCA | 27342 |
| rs774207277 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731532 | GACCAGCCTGGGCAA[C/T]ATGGTGAAACCCTGT | 27342 |
| rs774212266 | snp | A/C | | | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760526 | TCACTTCATCACAAC[A/C]TCTTCCTCCCGGGTT | 27342 |
| rs774220880 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700271 | CAGCCCTACTGGGCC[A/G]GAGCTTGCTCTCTGC | 27342 |
| rs774287654 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696525 | TCAAACCCTGTCTCT[A/C]CTAAAAATACAAAAA | 27342 |
| rs774288885 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793470 | AATTTGGGATTTTTG[A/G]GCATTTCAGATTTTT | 27342 |
| rs774291145 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772349 | GCTCCTTGGAGTGGA[A/C]GAATGGAGATAGGCA | 27342 |
| rs774313081 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761276 | ACTCAGTCCCCATGA[A/G]TGCCCCTCCTAACCC | 27342 |
| rs774343555 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735592 | AGAGGTGACAGGATC[A/G]TTGTGGGGGGGGTTT | 27342 |
| rs774376506 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752292 | ACAAGGTCAGGAGTT[C/T]GAGCCCAGCCTGGCC | 27342 |
| rs774379945 | snp | A/G | 0.000131904 | 0.00812002 | missense | RABGEF1 | GRCh38.p7 | 7:66805319 | CCACGCCTTCAGTCT[A/G]ATATCCAGTATATCA | 27342 |
| rs774413009 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794902 | TGATTCAGTGGATTA[C/G]ATAAATAGAAATGTA | 27342 |
| rs774415224 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719157 | CAGTAGGGAACGGCA[A/G]TTAACACCAAAAACC | 27342 |
| rs774431390 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727082 | CTAAAAACCACTGAA[A/T]GGTACACTTTAAATG | 27342 |
| rs774463861 | snp | G/T | 3.3264e-05 | 0.0040781 | intron-variant, missense | RABGEF1 | GRCh38.p7 | 7:66783727 | CCGGCAAACCAGCAT[G/T]GAAACGGATAGAGTG | 27342 |
| rs774469624 | snp | C/T | 1.71272e-05 | 0.00292632 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808842 | ATCGACTCGAGTATG[C/T]ATAGCTTTCCTAATA | 27342 |
| rs774484194 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779826 | CTTTCATCTTACACA[C/G]GGAATCCCTATTGGC | 27342 |
| rs774492268 | snp | C/T | 1.64795e-05 | 0.00287045 | missense | RABGEF1 | GRCh38.p7 | 7:66808962 | ATTTTGATCGCTACA[C/T]GTCTGGCCAGACCTC | 27342 |
| rs774499621 | in-del | -/T | | | intron-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66811835 | TTCAGATCCCTCAGC[-/T]GTGAAATGGGGTTAA | 27342 |
| rs774507329 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751262 | TCTCGATCTCCTGAC[C/T]TCAGGTGATCCGCCT | 27342 |
| rs774508908 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749389 | CTGTGTTTCCTTAAT[C/T]GTATATCCATAAAGC | 27342 |
| rs774562219 | snp | G/T | 1.79219e-05 | 0.00299344 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783636 | CCATGCATGGATCTT[G/T]TATGTCATGAAACTT | 27342 |
| rs774572101 | in-del | -/T | 2.50066e-05 | 0.00353591 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797335 | AAGAGAGAGAAAAAA[-/T]ATATATATCTTGATC | 27342 |
| rs774580786 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717343 | TACTATGTTGTAGTT[A/G]TCATATGTATTGCAT | 27342 |
| rs774590918 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780934 | GTATTTTTATATTTA[A/G]AGTTAATTTCTTACA | 27342 |
| rs774671470 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721093 | CCGGCTAATTTTTGT[A/G]TATTTAGTAGGGATG | 27342 |
| rs774703298 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700481 | GACTGAGGGCCAAGC[A/G]GGCCCCGGAGGGGGA | 27342 |
| rs774747680 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762320 | TGGAGGCTGGGTGCA[A/G]TGGCTCATGCCTATA | 27342 |
| rs774764760 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802022 | TCAAGCGATCCGTCC[A/G]CCTCAGCCTCCTGAG | 27342 |
| rs774766585 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801427 | ACTTTTTAATGTACA[A/G]TTAAATTACTTTTGA | 27342 |
| rs774830869 | snp | A/G | 3.29522e-05 | 0.00405894 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795619 | AGCCATTGAGAGATT[A/G]CGGGTATTGCACAGG | 27342 |
| rs774927016 | snp | A/G | 0.00116962 | 0.0241545 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797324 | AAAAAAAAAAAAAGA[A/G]AGAGAAAAAATATAT | 27342 |
| rs774928712 | in-del | -/GTGA | 4.95692e-05 | 0.00497816 | splice-donor-variant | RABGEF1 | GRCh38.p7 | 7:66805397 | TATTTCACCAATCTG[-/GTGA]GTAAGTGAGTTCTTG | 27342 |
| rs774936740 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683803 | TGGAGTACAGTGACA[C/T]GATCACGAGTCACTG | 27342 |
| rs774937207 | snp | A/T | 0.000288559 | 0.0120082 | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66756092 | GGTGAGTACTGAAAG[A/T]TATATAAGAAGAATA | 27342 |
| rs774937914 | snp | A/G | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754129 | TGCCTCACCTCCCGC[A/G]TAGCTGGGACTACAG | 27342 |
| rs774941950 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66744667 | GCCAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 27342 |
| rs774954943 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788084 | GCTTGTCCTGCTTTT[A/G]AAGGGGGCAGGCTCT | 27342 |
| rs774963142 | snp | C/T | 1.64955e-05 | 0.00287184 | missense | RABGEF1 | GRCh38.p7 | 7:66809174 | GACATCGTTGAGAAA[C/T]ACCCACTGGAAATTA | 27342 |
| rs774977137 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716096 | TGTCAGTTTTGCTGT[A/G]TATATTTGAGGTCTG | 27342 |
| rs774994885 | snp | C/G | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755676 | AGGCTACGGTAGCCA[C/G]ATTATCTTGTATGTA | 27342 |
| rs775030619 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66764497 | CTTTTGTTGCTCCTG[C/T]TTTTGGTGCCATATC | 27342 |
| rs775031230 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799513 | AAAATGCAGATTGTC[A/G]AAGGTACATTGGAAT | 27342 |
| rs775050445 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800106 | GGCCTTGGAAAGGCT[A/T]GTTCATGTAGACATT | 27342 |
| rs775058017 | in-del | -/TG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691361 | CTAAAAGTACAAAAC[-/TG]TACACAGCCCAGATG | 27342 |
| rs775061765 | snp | C/T | | | intron-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758478 | TCAACCAAGCTTCTA[C/T]TTATTGGAATGCAGT | 27342 |
| rs775063030 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66701926 | ATACATGACATAAAA[C/T]GGATCATCTTAACCA | 27342 |
| rs775063482 | in-del | -/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736026 | CCACTGTCACAACTT[-/G]TATTTAGCATTGCAC | 27342 |
| rs775071599 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711688 | GCCTCCTGGGTTCAA[A/G]CCATTGTCCTGCCTC | 27342 |
| rs775074951 | in-del | -/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737228 | ATTTAATTTTTAGGT[-/G]TTTTTTTGTTTCTTG | 27342 |
| rs775087200 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731020 | TTCGGGGCCAGGCTG[C/T]GGGCCTCCTGGTTCC | 27342 |
| rs775107000 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810744 | ACCGTTCTAGAACAA[C/T]GTCACTTCACACAGG | 27342 |
| rs775136735 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807045 | CAACCTGGAAGTCCC[C/T]GAGAAGTGTGAAGGT | 27342 |
| rs775228767 | snp | C/G | 0.000260247 | 0.0114042 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773688 | TGTTTGTTTTTGAGA[C/G]AGGGTCTTGCTCTGT | 27342 |
| rs775235380 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773859 | TATGTAGAGACAGGG[C/T]TTCACCATGTTGCCC | 27342 |
| rs775237035 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703044 | AGTGGTGCTATCTCA[A/G]CTTACTGCAAGCTCT | 27342 |
| rs775247067 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66786430 | TTTTTTTGAAGCAGT[A/G]TGTTGCTCTATCTCC | 27342 |
| rs775268492 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696415 | GACCGTGGGGCTGGG[C/T]GTGGTGGCTCACGCC | 27342 |
| rs775285979 | in-del | -/CAGA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726099 | CAGGAAGCTGCTACT[-/CAGA]CAGACAGGGCCAGAA | 27342 |
| rs775347226 | snp | A/G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796062 | GAATTGCTTGAACCC[A/G/T]GAAGGCGGAGGTTGC | 27342 |
| rs775357225 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779919 | CTCTCTAATCCAAAC[C/T]TCTGGCCTCTTAGTA | 27342 |
| rs775361656 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721830 | AATTTAGGTGGTTTG[C/T]CTTTTTACTTCCTTG | 27342 |
| rs775366597 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738162 | AGTAGCTGGGATTAC[A/G]GGTACAGGCCACCAC | 27342 |
| rs775413472 | snp | C/T | 3.29609e-05 | 0.00405948 | missense | RABGEF1 | GRCh38.p7 | 7:66808979 | TCTGGCCAGACCTCT[C/T]CCAGGAAGCAAGAAG | 27342 |
| rs775415386 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686718 | AGGAAAACATTATAG[C/T]TTTTGGTGCTGTTTT | 27342 |
| rs775432101 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761478 | AGGAGATGCTGGGGG[C/T]GAGGAATGGGGGAAG | 27342 |
| rs775510494 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66748933 | ACTCTCCAAAAACTG[-/T]TTTTATGTCATAAGA | 27342 |
| rs775523306 | snp | C/G | 1.72829e-05 | 0.00293959 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775215 | TCATTCTAATCCTCT[C/G]TTGAATTGCAGACTC | 27342 |
| rs775527233 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808510 | TGAGGCACCGGGCCC[A/G]GTCTGGAGCTGTTCT | 27342 |
| rs775538050 | snp | A/G | | | intron-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758609 | GGAGTTGAGTCTCAC[A/G]CAGCTGATCCCCCAT | 27342 |
| rs775559439 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728315 | CTATTGTCTTGTGGA[C/G]AGCCAGATGCTCTTC | 27342 |
| rs775563784 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810796 | CTTTTCCAGTATCTT[-/C]CTAAGGATGGAGCCC | 27342 |
| rs775625833 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769262 | GTGCACAGTGCATAC[G/T]GTCCAGATTTGATAG | 27342 |
| rs775633160 | snp | C/T | 5.26579e-05 | 0.0051309 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783881 | AACATAGAGTTTTGG[C/T]TTGAGGAAAGGTCTT | 27342 |
| rs775664308 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736734 | GGTGTGGTGGCTTGC[A/G]CCTGTAATCCCAGCT | 27342 |
| rs775685797 | in-del | -/AA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696701 | CTCAAAAAAAAAAAA[-/AA]AAAAAAAAAAAGAAA | 27342 |
| rs775689138 | in-del | -/GCGGTAGTCA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66781663 | TCCTCATACACATGT[-/GCGGTAGTCA]GCCACACTCAAGGGA | 27342 |
| rs775709985 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707405 | CTCTTTATTATTAAA[A/G]ATGAAGGCCAGGCAT | 27342 |
| rs775758089 | in-del | -/AC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802434 | AGAGATGGAGCGTAT[-/AC]TTAGCTCTGTGTTTC | 27342 |
| rs775763448 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778988 | GGTGTGGAAGTGTGC[A/G]CCTGTAATCCCAGCT | 27342 |
| rs775793835 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810441 | TGTCTCCTGGGGCCA[C/T]ATCACCCCTCCGTTA | 27342 |
| rs775798105 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66802212 | AGACATTTTTAAATG[C/T]CACAGCTGTGGGAGT | 27342 |
| rs775813773 | in-del | -/G | 1.85637e-05 | 0.00304656 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772115 | CGGTTGAACAGTGAC[-/G]TGACTGGATACATAG | 27342 |
| rs775820190 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777453 | ATTTAATATATATCA[C/T]AAATAATATATATAT | 27342 |
| rs775853611 | snp | C/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758132 | GAATGACCTCTGAGG[C/G]CATGACATTGAACCC | 27342 |
| rs775891638 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804649 | CTGAGGCAAGAGAAT[C/T]GCTTGAACCCAGGAG | 27342 |
| rs775915628 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693737 | CCGAGAGAGAGGACT[A/G]CGACCCTCAGGGAAT | 27342 |
| rs775920025 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790673 | TGATGTTTTTTCATC[C/T]AAATACTTTTGACTT | 27342 |
| rs775935632 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717745 | TTTTGTATTTTTCAG[A/C]GATAGGGTTTTGCTC | 27342 |
| rs775938026 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759265 | TTGTTACAGTGAGGG[A/G]ATACAAAGTAGGATT | 27342 |
| rs775962654 | snp | C/T | 1.67245e-05 | 0.00289171 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66771932 | ACGCCGAGGAATTCA[C/T]GTGGATCAATCGGAT | 27342 |
| rs776070039 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688579 | TATTTTATAATCGTC[A/G]TGGAATGAAACTAGA | 27342 |
| rs776091172 | snp | A/G | 1.65012e-05 | 0.00287234 | missense | RABGEF1 | GRCh38.p7 | 7:66809186 | AAATACCCACTGGAA[A/G]TTAAGCCTCCGAATC | 27342 |
| rs776111292 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788320 | CATGGTGGCGCTCGC[C/T]TGTAGTCCCAGCTAC | 27342 |
| rs776112264 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775861 | GAAGTGTATTGAGAA[C/T]ATATAGGAAAAGGCC | 27342 |
| rs776113848 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66776211 | CTGGGAGCCCCCTCA[C/G]TTGCTCCCCAGTTCC | 27342 |
| rs776121189 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733673 | ACTGCACTCCAGACT[A/G]GGCTACAGAGTGAGG | 27342 |
| rs776133857 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732756 | GTCTCTCTCGCTCTC[G/T]TGCTGTCTCTCTTTC | 27342 |
| rs776138570 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745085 | TAGTCTCAGTTACTC[A/G]GGAGGCTGAGGCAGG | 27342 |
| rs776154567 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804087 | ATTCCAGTAGCTGGA[-/T]TTTTTTTTTTTTTTT | 27342 |
| rs776157660 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745640 | CAGGCATGGTGATGT[C/G]CGCCTGTGATCTCAG | 27342 |
| rs776169482 | snp | A/G | 1.87905e-05 | 0.00306511 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771841 | AGATTTTATTTAGTA[A/G]AATGATAATTCATTT | 27342 |
| rs776176843 | snp | A/G | 1.77855e-05 | 0.00298202 | utr-variant-3-prime | RABGEF1 | GRCh38.p7 | 7:66809298 | GATCACAATTTAGTG[A/G]AGAGTATTTATTTGA | 27342 |
| rs776191843 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692864 | TGCTGAGAAGTCAGC[G/T]GGCTCCTGGCACCTA | 27342 |
| rs776202872 | in-del | -/AA | | | intron-variant, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66685502 | TCTACAAAAAAAAAG[-/AA]AAGATTCTTGAAGTG | 27342 |
| rs776208194 | in-del | -/AG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66688257 | TATGCACCTAACAAC[-/AG]AGCACCAAAACATAT | 27342 |
| rs776310233 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762588 | GGTGAGACCCTGTCT[C/T]AAGAAAAGAAAAGAA | 27342 |
| rs776326672 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66691488 | AAAATATGCTGAGTG[-/A]AAAAAAATTGGACCC | 27342 |
| rs776333330 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732055 | GGGCCAGGGCTGCCA[C/G]CCACCCCCAGCCCAG | 27342 |
| rs776334061 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66790564 | TGGGCAGCCCCTTAG[C/T]GCCGCCCTTGTTGAT | 27342 |
| rs776351688 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808618 | GGTGGGGATAGCAGG[C/T]CTGGGAAGACTCAGA | 27342 |
| rs776367105 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807314 | AGCTGACGAACCCCA[C/T]GGGCACTCACAGTCT | 27342 |
| rs776370936 | snp | C/T | 4.95626e-05 | 0.00497784 | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66797435 | CATCATGACTCGTCT[C/T]TATAAATATGTATTC | 27342 |
| rs776374227 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702012 | CATCACTACCATCAA[C/T]TCAAAAAGGGCAGGG | 27342 |
| rs776376396 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716063 | TAATTTTGAGTTTGT[C/G]TATTTCTCCTCAAGT | 27342 |
| rs776421177 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66793944 | TTGTTCTCGGCCTTA[C/T]TCATGTTCTTCTACT | 27342 |
| rs776433483 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769590 | TTCCTTGGCCTGGAC[A/G]TAGATGCATTGCAGA | 27342 |
| rs776464283 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66703252 | GCTGGGATTACAGGT[A/G]TGAGCCACCGTGCCT | 27342 |
| rs776481475 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712450 | TATTTATAGTTTTAA[A/G]TATTTTTCTTTCTGC | 27342 |
| rs776503112 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66769642 | TTACAGTTGCTTTTG[C/T]AGGAGAGGATTTATT | 27342 |
| rs776512339 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66722196 | CCTGTAATCCCAGCA[C/T]TCTGGGGGGCTGTGG | 27342 |
| rs776533375 | in-del | -/TC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799307 | AGCTCTTGTTTACTG[-/TC]TCTCTCTCTCTTTAG | 27342 |
| rs776536031 | snp | A/G | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754489 | GGGCTTATACCCGTA[A/G]TCCCAGCACTTTGGA | 27342 |
| rs776550837 | snp | C/T | 1.64798e-05 | 0.00287047 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795472 | TGTGCTTCTGCACTT[C/T]GTTCAGCTACAAGCA | 27342 |
| rs776563927 | snp | C/G | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680592 | CCTAGCACACATTAG[C/G]CACCTAGGAAGAATT | 27342 |
| rs776574418 | in-del | -/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66727903 | TGGCTGCCTCTGGAG[-/C]CTTTTGCCACCATGC | 27342 |
| rs776582758 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66751747 | CTTGAGAACAATGAG[A/G]TTGCTGAAAATTTCA | 27342 |
| rs776603424 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723559 | TATTTTTTCTTTAAA[A/C]AATTACTGTTTTTTT | 27342 |
| rs776611994 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759569 | GTTTAATTGGCTCAC[A/G]GTTCTACAGGCTGTA | 27342 |
| rs776628249 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683892 | ACTGCAAATGGGTGC[C/G]GCCACACCCAGCTGA | 27342 |
| rs776631924 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707086 | CACCGCGCCCGGCCC[A/G]TACTGGTTATTTTTG | 27342 |
| rs776635900 | snp | C/G | 1.68032e-05 | 0.0028985 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66775243 | CTCCAGCGGGAGGAA[C/G]AAGAGGCCTTTGCCA | 27342 |
| rs776652255 | snp | C/T | 1.65031e-05 | 0.00287251 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66775332 | AACCAACGAGAAGAC[C/T]CGCAAGGTTACCACA | 27342 |
| rs776682107 | in-del | -/TA | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66739976 | CTTCTGGATGTCGGT[-/TA]TATGTTTTTTTTGAG | 27342 |
| rs776682330 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700192 | TTCTGGATCCAAGCA[C/T]TGAGATCTCTCCCTA | 27342 |
| rs776685994 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746415 | TTCAAGGATTCTTCT[A/G]CCTCAGCCTCCCGAG | 27342 |
| rs776688152 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66738412 | CTGTCTTTAGCACCA[A/G]CCTCTTCTGCTCAGC | 27342 |
| rs776699486 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770749 | TTGGCCTCCCAAAGT[A/G]CTGGGATTACAGGCA | 27342 |
| rs776703804 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702852 | GTTCAGTTTTGAGAG[-/T]TTTTTTATATATTCT | 27342 |
| rs776717765 | snp | A/C | | | intron-variant, nc-transcript-variant | RABGEF1 | GRCh38.p7 | 7:66685381 | GAAGTGAGGCCAGGC[A/C]TGTTGGCTCACGCCT | 27342 |
| rs776774409 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66752717 | CCTTTCCCAGGCCAG[C/T]TGAATCAGAAACTCT | 27342 |
| rs776805837 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759945 | AATCAGGTGTTTACC[A/G]TAAATCATACAGTTT | 27342 |
| rs776820775 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726095 | GTCTGCAGGAAGCTG[C/T]TACTCAGACAGGGCC | 27342 |
| rs776856982 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699134 | ATTCCAGGCCCCTCT[A/G]GGTTTCCTCGTGGGT | 27342 |
| rs776880850 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740218 | ACTCAAGCGATCCTC[C/T]TGCCTGGGCCTCCTA | 27342 |
| rs776881770 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728391 | GTATCCCCCCTATGG[C/T]TGGGTCAGCTTCGAG | 27342 |
| rs776900469 | snp | A/G/T | 1.78198e-05 | 0.00298489 | splice-acceptor-variant | RABGEF1 | GRCh38.p7 | 7:66771882 | TTTCTTGTTTGTTCA[A/G/T]TGGTTAGCAGGAAGA | 27342 |
| rs776933967 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66686982 | ACCCACCACCACGCC[C/T]GGCAAATTTTTTATA | 27342 |
| rs776934045 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792199 | ACTCACTGCTCTACT[A/G]TCTTTTTTTCTTGGA | 27342 |
| rs776946126 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798597 | AGTTAGGGTGGGACC[A/G]GGAAACACACAGTGA | 27342 |
| rs776968008 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695316 | GACCCTGTCTCAAAA[A/G]AAAAAGGACCTCGAG | 27342 |
| rs776987784 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734722 | ACAGGTGTGAGCCAC[C/T]GTGCCTGGCCCCAAA | 27342 |
| rs776989065 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735342 | CTGTTCCCTTAGACT[A/G]TGTTTTATGGAAGAC | 27342 |
| rs777010316 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747372 | CTGTTTCACCCTAAG[A/G]AATGGTTTGGCAGCA | 27342 |
| rs777056278 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778323 | TAAGGAATTTGAAGA[A/G]TATCTTCACATTCTT | 27342 |
| rs777059784 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807256 | TCTGTCTCCTACACC[C/T]ATTGCTCCAATGAAA | 27342 |
| rs777066712 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730052 | TCAGTGTTTCAGCTG[C/T]GCCATAGACTCAGGG | 27342 |
| rs777077806 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747836 | TATCATTTACTTATT[A/C]CATTATTCCACATCT | 27342 |
| rs777112674 | snp | C/T | 1.64852e-05 | 0.00287094 | missense | RABGEF1 | GRCh38.p7 | 7:66809007 | AAGCTGAGAGTTGGT[C/T]TCCTGATGCTTGCTT | 27342 |
| rs777130707 | snp | A/G | 1.69069e-05 | 0.00290743 | intron-variant, missense | RABGEF1 | GRCh38.p7 | 7:66783777 | TTCTCAAGACCTTCC[A/G]CAAGACAGGCCAAGA | 27342 |
| rs777163914 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708265 | CTTTGTTTATAGCCA[C/T]GTAGTTTGGGTTTTT | 27342 |
| rs777189102 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796105 | CTGTGCCACTGCACT[C/G]CAGCCTGGGCAACAG | 27342 |
| rs777281207 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734394 | TCACCCTCTTTGAGC[C/G]TCTGTTTCCTCGTCT | 27342 |
| rs777347261 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782173 | AATATTTTAGAAAAG[-/A]TGTTGCATTTTTTGT | 27342 |
| rs777350097 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792848 | GGTGAACAGTGCCCT[C/T]GTGGAGCTAACATTT | 27342 |
| rs777374661 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719024 | CAGCAACAGGAATCC[C/T]TCCAGCACTCTTGGG | 27342 |
| rs777434083 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718679 | CTTCGCAGTATTCAG[A/C]TATGTCCTGAGTATG | 27342 |
| rs777458020 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66777059 | TAGCACAGTGCCTGA[C/T]ACACACAGTAGATCT | 27342 |
| rs777476463 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767098 | ACCTCCATCTCCCCG[A/G]TTCATGCGATTCTTG | 27342 |
| rs777477165 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797985 | AGCCAGGCATGGTGG[C/T]GCACGCCTGTGATCC | 27342 |
| rs777495586 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773410 | GGGGTCCCGATTCCA[C/T]CCTCAGACTTAGCAC | 27342 |
| rs777511369 | snp | A/G | 4.9467e-05 | 0.00497303 | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66809035 | CTTAGGCGTCAAGCA[A/G]ATGTATAAGAACTTG | 27342 |
| rs777518173 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66707101 | GTACTGGTTATTTTT[C/G]AAGTATGTTGATTAG | 27342 |
| rs777527874 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725210 | TCAAGATACACTTTA[C/G]TTTACCATACAATTC | 27342 |
| rs777554970 | snp | A/G | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755112 | ATCCTGGCTAACACA[A/G]TAAAACCTGGTCTCT | 27342 |
| rs777566427 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779168 | AATAAATGAAGTATA[A/C]CTGATTGAACAAAAA | 27342 |
| rs777569138 | in-del | -/CTC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729439 | GTCCTCCCGTCTATT[-/CTC]CTCTCCAACCTCACT | 27342 |
| rs777579269 | snp | A/G | | | intron-variant, downstream-variant-500B | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66760772 | AACATAATGGCTAAT[A/G]CTCACGAGGGGAAGA | 27342 |
| rs777599228 | snp | C/T | 0.000151445 | 0.00870054 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783857 | GTAGGTTGAGAATAA[C/T]CACGTAGAAACATAG | 27342 |
| rs777667245 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66735144 | TTTTAGTGTTAGATA[C/T]AAAGTGTTAGCTAAT | 27342 |
| rs777684261 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684794 | CACCCGCCACCATGC[C/T]TGGCTAATTTTTTGT | 27342 |
| rs777685946 | snp | C/T | 4.94368e-05 | 0.00497152 | missense | RABGEF1 | GRCh38.p7 | 7:66808955 | CAGGAGGATTTTGAT[C/T]GCTACATGTCTGGCC | 27342 |
| rs777704419 | snp | A/C | 1.66217e-05 | 0.0028828 | intron-variant, missense | RABGEF1 | GRCh38.p7 | 7:66783720 | CCATAAACCGGCAAA[A/C]CAGCATTGAAACGGA | 27342 |
| rs777744171 | in-del | -/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779638 | GATCATGCAACCGTA[-/C]TCCAGCCTGGGTGAC | 27342 |
| rs777751907 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780629 | CCTCTCTGTCAATTA[A/C]TAAATGAGGAATATT | 27342 |
| rs777758521 | in-del | -/CA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66687483 | TTCTGTTGTTTAAGC[-/CA]AAAAAAAAAAAAAAA | 27342 |
| rs777812521 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726643 | AAGTGCTGGGATTAC[A/G]GGCATGAGCCACTGC | 27342 |
| rs777814946 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800597 | CCCGCACCTTTTGCT[C/T]GGGGAACCCCATAAG | 27342 |
| rs777841771 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783074 | GTGTAGTGCATGTTT[A/C]CCTTGTCTCTTCATT | 27342 |
| rs777853582 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710951 | AGTTTGAGACCAGCC[A/T]GGGCAACATAGCGAG | 27342 |
| rs777878698 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683386 | ATAACATTTTGCTTT[A/T]AAGAGTTACTGATTC | 27342 |
| rs777884139 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692163 | ACTCGGTAGCTCTAC[C/T]GGCTGCCATACTGAA | 27342 |
| rs777903592 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66762873 | AGCTTAGACCTAAAC[A/G]ATGAGAAACAAACCA | 27342 |
| rs777914147 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715488 | TAATTTGGCGGCATC[A/G]TGTAAGTTTTGACAT | 27342 |
| rs777959279 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66765606 | CGTACAGGACCTTCT[A/G]CTTTTCTCTGCTTCT | 27342 |
| rs777961590 | snp | A/G | 3.5184e-05 | 0.00419413 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775199 | TTGGAGAATATCTAG[A/G]TCATTCTAATCCTCT | 27342 |
| rs778001232 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66720957 | GAGTCTTACTCTGTC[A/G]CCCAAGCTTGAGTGC | 27342 |
| rs778005567 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774562 | GCTTGCACATTTGTA[A/G]TTCCTTCTTTCTGGA | 27342 |
| rs778011879 | in-del | -/TCTC | 5.19184e-05 | 0.00509475 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799308 | AGCTCTTGTTTACTG[-/TCTC]TCTCTCTTTAGAGCC | 27342 |
| rs778029548 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763072 | GTGCAGTCATAGCTC[A/G]CTGCAGCCTCAAATT | 27342 |
| rs778036678 | snp | A/G | 1.66607e-05 | 0.00288619 | missense | RABGEF1 | GRCh38.p7 | 7:66797385 | TCAGTGCCTCCAGAA[A/G]GAGTCGAGAAGATAA | 27342 |
| rs778056930 | snp | C/T | 1.68241e-05 | 0.00290031 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66772037 | AGAGTACCACAAAGC[C/T]AGGCAGAAGCAGATT | 27342 |
| rs778122141 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66774738 | ACACTCCAGCCTGGG[C/T]GATGGAGTGACACTC | 27342 |
| rs778159140 | in-del | -/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66807504 | CTCTGCATCTCTCTT[-/C]CTGCACCATCTTCTC | 27342 |
| rs778162251 | snp | A/G | 1.66029e-05 | 0.00288117 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775397 | GATCAAAGAAGGGTA[A/G]TGTTCTGATACTCTT | 27342 |
| rs778185835 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66711735 | GGAACTACAGGTGCC[G/T]GACACCATGCCCGGC | 27342 |
| rs778228037 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721045 | GCCTGAAACCTCCAG[A/C]GTAGCTAGGATCACA | 27342 |
| rs778230989 | in-del | -/TTTAC | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775600 | TTTTAGAGAAATTTG[-/TTTAC]TTTATAGGAGGAATC | 27342 |
| rs778241301 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742663 | CAGGCTGGAGTACAG[-/T]TGACACGATCACGAG | 27342 |
| rs778289327 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794086 | CATCCTAGTGATGGT[A/T]GCTAAAAAATTTAGT | 27342 |
| rs778309714 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697692 | TGGGGCTGGGGGAGG[C/T]GCAGACTGTGTTCTC | 27342 |
| rs778330159 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773723 | CTGGCTGGAGTGCAA[C/T]GGTGCAATTTCAACT | 27342 |
| rs778334810 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737588 | AAAAAAAAGATGAAA[A/G]ACTGATATAGTGCTG | 27342 |
| rs778350668 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684882 | CCTCGTGGTCTGCCC[A/G]CTTCGGCCTTCCAAA | 27342 |
| rs778350718 | snp | A/G | 4.99097e-05 | 0.00499524 | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66799407 | TATGGTGGTGAAGGC[A/G]ATCACAGGTCAGTGA | 27342 |
| rs778355553 | snp | A/G | 1.66576e-05 | 0.00288592 | missense | RABGEF1 | GRCh38.p7 | 7:66809240 | GAAAACGTTGAAAAT[A/G]ATAAACTTCCTCCAC | 27342 |
| rs778383137 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799966 | CAGGTCCAGCCTCCT[A/G]ATAAGGTTTGTTTCT | 27342 |
| rs778489645 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779277 | GGGAGGCCGAGGCAG[A/G]TGGATCACCTAAGGT | 27342 |
| rs778490355 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778264 | AGGAAAGTTTTTATG[C/T]CATACGTAGCAGCTT | 27342 |
| rs778507301 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66767310 | GCCCAGCCGAGGTTT[C/T]TTTTTTGTTTAAATC | 27342 |
| rs778516606 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723780 | TGACGGGGTTTCACC[A/C]TGTTGGTCAGGCTGG | 27342 |
| rs778572706 | snp | A/G | 6.60677e-05 | 0.00574713 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66775310 | TCTCCAAGTTTGAAG[A/G]AAAGAAAACCAACGA | 27342 |
| rs778596243 | in-del | -/AG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705444 | TCCATCTCGAAAGAA[-/AG]AGAGAGAGAGAGAGA | 27342 |
| rs778665488 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714412 | TTTGTAGTGATATCA[C/T]GTATTTCATTCCCAA | 27342 |
| rs778669041 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702993 | TGTTTGTTTTTGAGA[A/T]GGAGTCTCGCTCTGT | 27342 |
| rs778706191 | snp | C/T | 1.64732e-05 | 0.0028699 | utr-variant-5-prime, stop-gained | RABGEF1 | GRCh38.p7 | 7:66795544 | CAGTCAGAGTGTGCT[C/T]AGGATTTCTACCACA | 27342 |
| rs778724225 | snp | A/G | 1.64844e-05 | 0.00287087 | | | GRCh38.p7 | 7:66809144 | TGGACAGATGGAATT[A/G]CAAGAGAAGTTCAAG | 27342 |
| rs778774515 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800698 | AGAAAGTTCAAGATC[A/G]GCTGGTTTACATTTA | 27342 |
| rs778848440 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731564 | TCTCCAGAAAAAAAA[A/T]AAATTAGCTGGGTAT | 27342 |
| rs778926596 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768079 | ACTATAACCGTTTGC[A/G]TATAGAATTTTGTAA | 27342 |
| rs778947991 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715774 | TTAGAGATGGGTCTC[A/G]GCTGTGTTACCTAAG | 27342 |
| rs778961094 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66808350 | TCTCCCAGGTAGCGG[A/G]GATTACAGGCGCCCA | 27342 |
| rs778973257 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66740851 | GCTACAGGAGCGGGG[A/C]GGCGGGGCGTCTCGG | 27342 |
| rs778993139 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66692165 | TCGGTAGCTCTACCG[G/T]CTGCCATACTGAACA | 27342 |
| rs779042495 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66787740 | CACTTATGAAGAGGT[A/G]TACATTCTCTTTGTC | 27342 |
| rs779043088 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66704031 | CAATTTATTCCTAAG[C/T]GTTTTATTGATTTTG | 27342 |
| rs779058883 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742606 | ACTACAAGGAGGTGC[C/T]TATTAATTTATTTAT | 27342 |
| rs779069015 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714733 | GAGGTCAGGAGATCA[C/T]GACCATCCTGGCTAA | 27342 |
| rs779069490 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796576 | CCAACAGTTGGAAGA[A/T]GATTTTTTTGTTTGT | 27342 |
| rs779083264 | in-del | -/TCTTGGTTGTGTTTTTTG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737997 | TTAAAGCTGCAAGCT[-/TCTTGGTTGTGTTTTTTG]TTTTTTTTGTTTTTT | 27342 |
| rs779088237 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66746350 | CTCTGTTGCCCAGGC[-/T]TGGAGTGCAGTGGCG | 27342 |
| rs779131949 | snp | A/G/T | 4.94771e-05 | 0.00497358 | synonymous-codon, missense | RABGEF1 | GRCh38.p7 | 7:66809059 | GAACTTGGATCTCTT[A/G/T]TCTCAGTTGAATGAA | 27342 |
| rs779148612 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775750 | TACCCTCACTGTTCA[A/T]AGCTTGTCAGAAATG | 27342 |
| rs779157835 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795993 | AAAATACAAAAAGTA[G/T]CCGGGTGTTGTGGTG | 27342 |
| rs779158124 | snp | A/G | | | synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66808990 | CTCTCCCAGGAAGCA[A/G]GAAGCTGAGAGTTGG | 27342 |
| rs779160342 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782254 | CCAAATGGTTCTAGC[A/C]TAAGAGGTATGGTCA | 27342 |
| rs779180932 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66753491 | GTTTGGTTCTGCACC[A/G]CTGTAATAAAGTGAG | 27342 |
| rs779252122 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729291 | CGCCTTCATCCTCCC[C/T]TCCATCCTCCCCTCC | 27342 |
| rs779263753 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763236 | TGGGTATTCTGCTGA[A/G]GACCTCAGGAGGTCA | 27342 |
| rs779271516 | in-del | -/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782780 | GACAGAGCAAGACTT[-/C]GTCTCAAAAAAAAAA | 27342 |
| rs779284624 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66737892 | TGCTGCTCGGTGCCT[A/C]GAACATTCTTGCCCA | 27342 |
| rs779315869 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66698831 | TGACTCCACCCTGGT[A/G]CTCCTCCACCTTTCT | 27342 |
| rs779373519 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733848 | CTCTACCAAAAATAT[-/A]AAAAAAATTAGCCAG | 27342 |
| rs779396800 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66689290 | CAGGTCAGCAAAATC[A/G]ACAAGTTTTTAGCTA | 27342 |
| rs779426544 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803519 | TGCTTCAGCACCCTT[C/T]GCTGTCCCCCAGGCT | 27342 |
| rs779438863 | in-del | -/TG | 6.59055e-05 | 0.00574007 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795617 | TAGCCATTGAGAGAT[-/TG]TGCGGGTATTGCACA | 27342 |
| rs779465699 | snp | C/G | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680966 | CGGGCGCCTATAATT[C/G]CGGCTACTCGAGAGG | 27342 |
| rs779501520 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66712000 | TTACTTAATTACTTA[C/T]AGTAAGTCCTAAATT | 27342 |
| rs779507546 | snp | A/G | 1.65332e-05 | 0.00287512 | missense | RABGEF1 | GRCh38.p7 | 7:66797419 | ATCAGATTGAAAAGT[A/G]CATCATGACTCGTCT | 27342 |
| rs779538308 | snp | G/T | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759189 | GCAGTCCCCAGGGCT[G/T]CCCCCAGGTTTCGTA | 27342 |
| rs779553380 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66758259 | TCCAGAGCCTTAAGA[A/G]AGAACACTAATAGTT | 27342 |
| rs779578018 | snp | A/G | 1.6703e-05 | 0.00288985 | intron-variant, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66783691 | AATTCAGGAAGCAAA[A/G]GCTCCCAGTCCTTCC | 27342 |
| rs779591492 | snp | A/T | 3.49595e-05 | 0.00418073 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66771901 | TTAGCAGGAAGAAGA[A/T]GAGCCTTAAGTCTGA | 27342 |
| rs779612874 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66800857 | GAGTGTTTGTGTGAC[C/T]CATCAGTGGTGAAAG | 27342 |
| rs779617324 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66709999 | AATATTTTATTTTGC[A/T]TTCATTTTTAATTTT | 27342 |
| rs779617340 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66696051 | TGGACGTGGGCCTTA[C/T]AAGGGACTTTAAAAT | 27342 |
| rs779642842 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66768193 | ATTATATTTACTGTA[A/C]TGGACAGTTAACAAA | 27342 |
| rs779653765 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66736156 | CATTCACTCCTGCCT[C/T]AGATAGACTCAAGAC | 27342 |
| rs779703908 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66697335 | CGTCTCACAAGTCTT[G/T]CATTTCAGGCCTGCA | 27342 |
| rs779710184 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728109 | AGCAGCTCAGGGCTC[C/G]TTTGTGTCTGCTCAG | 27342 |
| rs779728708 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66780359 | AAGTTACTTAACATA[G/T]TCAAGCCTCAGCTTC | 27342 |
| rs779745577 | snp | A/C | 1.66913e-05 | 0.00288883 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775408 | GGTAATGTTCTGATA[A/C]TCTTTTTTTTCTTCT | 27342 |
| rs779766939 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66745712 | AGGCGGAAATTGCAA[C/T]GAGCCGAGATTGTGC | 27342 |
| rs779778302 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66685020 | TTCTCTAGCCTTGGA[C/T]TCCCAAAGTGTTGGG | 27342 |
| rs779817276 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66788439 | ACAGAGCAAGACTCC[-/A]TCTCAAAAAAAAACA | 27342 |
| rs779830379 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733055 | CAGCTCCTTAGCCGC[A/G]TAGTCAAGGTTCCTG | 27342 |
| rs779863337 | snp | C/T | 1.64836e-05 | 0.0028708 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795640 | ATTGCACAGGGATGA[C/T]TGCTCAGTCTCTTAG | 27342 |
| rs779878571 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66693336 | ATTTCCCCTTTATTG[C/G]AAACACGTTGAATAC | 27342 |
| rs779889590 | snp | A/T | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66680936 | AAATACGAAAAAATT[A/T]GCTGGGCATGGTGGC | 27342 |
| rs779900854 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789981 | TACTCCCTCTACGGA[C/T]AAGATACTCATGGAA | 27342 |
| rs779929456 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759003 | ACATGTTACATAACT[A/G]TAATGTAATGTCAAA | 27342 |
| rs780050510 | in-del | -/A | 0.32 | 0.24 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797329 | AAAAAAAAGAGAGAG[-/A]AAAAATATATATATC | 27342 |
| rs780082569 | snp | A/G | 1.64855e-05 | 0.00287097 | missense | RABGEF1 | GRCh38.p7 | 7:66809147 | ACAGATGGAATTGCA[A/G]GAGAAGTTCAAGACA | 27342 |
| rs780086819 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716967 | TATTTTTAGTAGAGA[C/T]GGGGTTTCGCCATGT | 27342 |
| rs780092625 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66723160 | TTTTAGTAGAGACGG[C/G]GTTTCACCATGTTGG | 27342 |
| rs780101668 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796914 | TTTTTTTTTAAGCGT[A/G]TTTTTAAATATAACA | 27342 |
| rs780111718 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763375 | GTCCTCATTTCTTTG[C/T]TGGCTGTCAGCCAGA | 27342 |
| rs780166678 | snp | G/T | 1.64732e-05 | 0.0028699 | missense | RABGEF1 | GRCh38.p7 | 7:66805247 | ACCAAGAATGAGCCG[G/T]CGTCAGCGGATGACT | 27342 |
| rs780247365 | snp | A/G | 1.64925e-05 | 0.00287158 | missense | RABGEF1 | GRCh38.p7 | 7:66809076 | CTCAGTTGAATGAAC[A/G]ACAAGAAAGGATCAT | 27342 |
| rs780268380 | snp | C/T | | | upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66682052 | CCTCCCGTCATCAGC[C/T]AAAGGCCCCGGAAGT | 27342 |
| rs780271085 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66695439 | AGACCGTCATGGGCA[G/T]GGGCTTTGACGCAAG | 27342 |
| rs780286779 | snp | A/C | 1.64743e-05 | 0.00287 | utr-variant-5-prime, missense | RABGEF1 | GRCh38.p7 | 7:66795570 | CCACAATGTGGCCGA[A/C]AGGATGCAAACTCGT | 27342 |
| rs780303011 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66782300 | GTTTGTCTCTTGCCC[A/G]TCTAGTTCCTAAGCA | 27342 |
| rs780303039 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798126 | CTTCTCAAAAAAATA[A/G]CAAGTCAGTAGATGT | 27342 |
| rs780305725 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66763954 | AAACATTCACGTACA[A/G]GTTTCTCTGTGGACA | 27342 |
| rs780310426 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715321 | ATTTTTGTAGATACC[A/G]TGTCTCATTATGTTA | 27342 |
| rs780324546 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66799307 | GAGCTCTTGTTTACT[A/G]TCTCTCTCTCTTTAG | 27342 |
| rs780365861 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724557 | TAGAGACAGGGTTTC[A/G]CCATGTTGGTCAGGC | 27342 |
| rs780393284 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719476 | GTGCTGGGATTACAG[A/G]CATGAGCCACCATGC | 27342 |
| rs780412366 | snp | A/C | 3.5084e-05 | 0.00418817 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66772084 | TGGCGGAGCGGTAAA[A/C]GGACTTAACTAGGGG | 27342 |
| rs780469171 | in-del | -/TTTGTATT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734454 | TAGTGTAAGCAATGA[-/TTTGTATT]TTTGTATTTTTTTTA | 27342 |
| rs780475696 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730298 | AGGAAGTCACTCACT[A/G]TTTCTGCTGAGCGCC | 27342 |
| rs780499224 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729546 | CAACCTCACCTTTAT[C/T]CTCACCTTCATCCTT | 27342 |
| rs780500652 | snp | A/G | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759080 | CATTTCATCTCATAC[A/G]TAGATTCCTGTAGCC | 27342 |
| rs780536666 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66690841 | AAAATTCCAGCACTT[C/T]GGGAGGCTGAGGAAG | 27342 |
| rs780559744 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66718499 | ATATTGGATAATTTT[C/G]AATTGTGTTTTGGAT | 27342 |
| rs780641910 | snp | A/T | 0.00259403 | 0.0359205 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773926 | CCGCCTTGGCCTCCC[A/T]GTGTGCTGGGATTAC | 27342 |
| rs780644891 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699789 | ACCCAGGAGGTTGAG[G/T]CTGCAGTGAGCCAAA | 27342 |
| rs780673269 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66801972 | GAGTGCAAGTGGCAA[C/T]GATCATGGCTCACTG | 27342 |
| rs780680722 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773248 | CTCCTCAGGGTTTCC[A/T]CTGCATGCCTGATGC | 27342 |
| rs780685810 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747753 | GCCATTAGAAATTGA[A/G]CATAGAAAATGTTTA | 27342 |
| rs780697992 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795920 | AAAGCAGGCGGATCA[C/T]GTTAGGCCAGGAGTT | 27342 |
| rs780745097 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805120 | TTCTCCTGGGAAATA[C/T]TGTCTTTTCTGCTTT | 27342 |
| rs780753766 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729082 | CAGCCTCCCGAGTAG[C/T]TGGGACTACAGGTGC | 27342 |
| rs780870013 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66770012 | GCATCCCCAAGTGGT[C/T]TCTCTATACTCCGTA | 27342 |
| rs780875324 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803340 | AAAGAACCCTTTGGT[A/G]TACCCCACCGCCTGG | 27342 |
| rs780877392 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715766 | TTTTTTTTTTAGAGA[C/T]GGGTCTCGGCTGTGT | 27342 |
| rs780892054 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740336 | AACAGAGTTTCTGAA[C/G]CGTCCCTCGGCGCAG | 27342 |
| rs780912399 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734131 | TCATTTCTCCACTCC[A/G]TACTTTTGAGGTATT | 27342 |
| rs780917572 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66683253 | AGAGTGCTGGGATTA[G/T]AGACGTGAGCCATTG | 27342 |
| rs780939846 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66798281 | CAGCACTGTGTACTC[C/T]AGTTGCGGTGGACAC | 27342 |
| rs780965416 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66724723 | GGTTCATGGTTTTCA[G/T]CAAATTTATAGTTTG | 27342 |
| rs781016578 | snp | C/T | 1.79686e-05 | 0.00299733 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771872 | TCAACAGCACTTTCT[C/T]GTTTGTTCAGTGGTT | 27342 |
| rs781035196 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66717177 | TATCAATTGATTATT[G/T]TATTATATCTCTTTG | 27342 |
| rs781069854 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66733316 | GGCTGCCCCACTTAG[A/G]CTGCTGTGCACCAAT | 27342 |
| rs781092514 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731698 | TCCAGCCTGGGTGAC[-/A]AGAGAGCGAGACCTT | 27342 |
| rs781111078 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66694999 | GTCAAGCCACAGGGT[A/G]GAGGAATGGCTCAGA | 27342 |
| rs781112400 | snp | A/C | | | intron-variant, upstream-variant-2KB | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66757122 | CTTACACATTTTGGA[A/C]TGTTTGACACTGTTA | 27342 |
| rs781132235 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66783905 | AGGTCTTAGAGATAA[C/T]ATAGTGCAACCTTGT | 27342 |
| rs781174085 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66778187 | ATTCTGTATTCTTGA[A/G]TCTTCCTTAGTCCAT | 27342 |
| rs781174893 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66803821 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 27342 |
| rs781195728 | snp | A/G | 1.65649e-05 | 0.00287788 | missense | RABGEF1 | GRCh38.p7 | 7:66809220 | CGTTAGCAGCTATTG[A/G]CTCTGAAAACGTTGA | 27342 |
| rs781207597 | snp | A/G | 1.65833e-05 | 0.00287948 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66805425 | TTCTTGGTGTTGTGG[A/G]GAAGGACTAGGAAGG | 27342 |
| rs781208930 | in-del | -/ATCCATAATTTCTG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784445 | ACACCTGTTTCTTTT[-/ATCCATAATTTCTG]ACCCATAATTTCAGT | 27342 |
| rs781212242 | snp | C/G | 0.000219853 | 0.0104823 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796861 | CTCCCAAAGTGCTGG[C/G]AATACAGGAGTAGAG | 27342 |
| rs781216440 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66713372 | TGACCTCGTGATCGG[C/T]CCGCCTTGGCCCTCC | 27342 |
| rs781226874 | in-del | -/CA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700214 | CTCTCCCTACCAGGG[-/CA]CCCAGCCAAGCCCCA | 27342 |
| rs781278437 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66708568 | TGCTAGGATTACAGG[C/T]GTGAGCCACCGCCCC | 27342 |
| rs781301023 | snp | C/T | 5.04681e-05 | 0.0050231 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775423 | CTCTTTTTTTTCTTC[C/T]CTGCCTGAGTGAGAC | 27342 |
| rs781306899 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66684147 | TGGGTCCTTATGTGG[-/T]TAAAATGGGTCTCCC | 27342 |
| rs781308053 | snp | A/G | 1.6492e-05 | 0.00287154 | missense | RABGEF1 | GRCh38.p7 | 7:66809162 | AGAGAAGTTCAAGAC[A/G]TCGTTGAGAAATACC | 27342 |
| rs781317612 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66810994 | ATAAGTTACTATCAA[A/T]TGCCAGTGAGAATCT | 27342 |
| rs781338543 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730310 | ACTGTTTCTGCTGAG[C/T]GCCAGCTTCCTCATC | 27342 |
| rs781357463 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773424 | ACCCTCAGACTTAGC[A/G]CCTCCACCTGTGATT | 27342 |
| rs781362270 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741407 | GGAGCAGAAGTCCCT[A/G]CTTCCGAACCGTCTG | 27342 |
| rs781372137 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797618 | AAAGCAATAGCTCAT[A/G]TTCCTGCTTCCTTAG | 27342 |
| rs781399666 | snp | C/G | 0.000164731 | 0.00907405 | missense | RABGEF1 | GRCh38.p7 | 7:66795577 | GTGGCCGAAAGGATG[C/G]AAACTCGTGGGAAAG | 27342 |
| rs781402721 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806767 | TCATGCCTTAGCCTC[A/C]CAAGTAGCTGGGATT | 27342 |
| rs781418035 | snp | A/G | 0.000296482 | 0.0121718 | missense | RABGEF1 | GRCh38.p7 | 7:66805217 | AGCAAGCACATCTTC[A/G]ATGCCATCAAGATCA | 27342 |
| rs781447827 | snp | C/G | 3.56125e-05 | 0.0042196 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66775183 | CACATACAGAGAAAC[C/G]TTGGAGAATATCTAG | 27342 |
| rs781452545 | snp | A/C | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66754993 | CAGCCTGGGAAATAT[A/C]GCTAGATCCTGTCTC | 27342 |
| rs781465645 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761801 | TCATGCCTGTAATCC[C/T]GCACTTTGGGAGTTT | 27342 |
| rs781505279 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66731421 | ACGCCTGGCTGGTAA[A/G]TAAGGATCTTGGAGG | 27342 |
| rs781514342 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66714043 | TGTTTTTGTACTACC[A/G]TAGTCTAGTTTTGAT | 27342 |
| rs781529330 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66749373 | ATATAGTTATGTAAT[A/G]CTGTGTTTCCTTAAT | 27342 |
| rs781558542 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742421 | TGGTAAGGAATGTGA[A/G]CTAAGATGGAGCACC | 27342 |
| rs781572110 | snp | A/G | 1.64738e-05 | 0.00286995 | missense | RABGEF1 | GRCh38.p7 | 7:66805211 | AAGTGCAGCAAGCAC[A/G]TCTTCAATGCCATCA | 27342 |
| rs781652824 | snp | C/T | 3.31137e-05 | 0.00406887 | utr-variant-5-prime, synonymous-codon | RABGEF1 | GRCh38.p7 | 7:66775290 | AGGGGCCCAATCCCT[C/T]ACATTCTCCAAGTTT | 27342 |
| rs781680328 | in-del | -/G | 0.00365931 | 0.0426176 | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797324 | AAAAAAAAAAAAAGA[-/G]AGAGAAAAAATATAT | 27342 |
| rs781683448 | snp | A/G | | | missense | RABGEF1 | GRCh38.p7 | 7:66809103 | TCATGAATGAAGCCA[A/G]GAAACTGGAAAAAGA | 27342 |
| rs781689113 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719626 | AGAAAACATAGAAGA[C/T]AATACTTCCCAAGTA | 27342 |
| rs781700232 | in-del | -/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66719718 | TCAGCAAACCATGGC[-/T]TTGTGGGGCCAAACC | 27342 |
| rs781748659 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66795600 | TGGGAAAGGTAACAC[A/T]GTTAGCCATTGAGAG | 27342 |
| rs781751953 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66779341 | AAACCCTGTCTCTAC[C/T]AAAAATACAAAAATT | 27342 |
| rs781758945 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773323 | GGCACAAACTCCCTC[A/G]GCTTCCTCCCCTCAC | 27342 |
| rs781776358 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66794513 | TTTAAATATTCTTTG[A/G]CAGAAAGTGAGAAAC | 27342 |
| rs796071948 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728891 | CCACTCTCATCTCCA[A/C]ACTCACCTCCACGCT | 27342 |
| rs796072492 | in-del | -/TG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773082 | CTCTAGCTAGTTGTT[-/TG]TTTTTTTTTTTTCAT | 27342 |
| rs796096124 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729528 | CACCTTTATCCTCAC[C/T]TTCAACCTCACCTTT | 27342 |
| rs796114447 | multinucleotide-polymorphism | AT/GA | | | utr-variant-5-prime, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66740590 | CGCTCGACCCTTTGG[AT/GA]CCACTCGCACTTCCT | 27342 |
| rs796150057 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729441 | CCTCCCGTCTATTCT[C/T]CTCTCCAACCTCACT | 27342 |
| rs796170723 | multinucleotide-polymorphism | CAA/GAG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66705447 | TCTCGAAAGAAAGAG[CAA/GAG]GAGAGAGAGAGAGAG | 27342 |
| rs796230504 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728836 | CTCAAGACCACCTTC[A/C]CCTACACCTACACGT | 27342 |
| rs796238883 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728771 | TCACCGCCATCCTCA[C/T]CTCCACCCTCACCTT | 27342 |
| rs796254898 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728861 | ACACGTCTATCCTCA[C/T]CTCCACCTTCAACTC | 27342 |
| rs796299088 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710923 | CAAGACAGGAGGATC[A/G]CTTGAGGCCAGGAGT | 27342 |
| rs796344374 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728847 | CTTCACCTACACCTA[C/T]ACGTCTATCCTCACC | 27342 |
| rs796362776 | in-del | -/TG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66702348 | GGCTATTGTTTTGTT[-/TG]TGTGTGTGTGTGTGT | 27342 |
| rs796368360 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728887 | AACTCCACTCTCATC[A/T]CCAAACTCACCTCCA | 27342 |
| rs796370244 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66730388 | AAAGGCATCTTAAAC[A/G]GTAGGTTATTATTAT | 27342 |
| rs796378755 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66721302 | TATATTAGTGTCTTA[C/T]TGCTACTCTAACATA | 27342 |
| rs796390963 | in-del | -/A | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66755303 | TGTCTCAAAAAAAAA[-/A]CAAAAAACAAAAAAC | 27342 |
| rs796418353 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728869 | ATCCTCACCTCCACC[C/T]TCAACTCCACTCTCA | 27342 |
| rs796421845 | in-del | -/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66742161 | ATCTCAAAAAAAAAA[-/C]TAAGAGTCTGTTCCT | 27342 |
| rs796438189 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728731 | GTCCTCACCTCCACC[C/T]TCACCTCCATCCTCA | 27342 |
| rs796443951 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728644 | CTCATCATCCTCGCC[G/T]CGACTTTCAGCTCTG | 27342 |
| rs796453879 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66700134 | TTGGGTGAAGGGAGG[C/G]ACGGAGGCCCAGCCA | 27342 |
| rs796464435 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66747853 | ATTATTCCACATCTT[G/T]TTCCAGAAAGGGTTT | 27342 |
| rs796465804 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728809 | ATCCTCACCTCCACC[C/T]TCACCTCCATCCTCA | 27342 |
| rs796499941 | in-del | -/AG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66804756 | AAAAAAAAAAAAAAA[-/AG]TGTGGGCTTTACAGT | 27342 |
| rs796505698 | snp | C/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728657 | CCTCGACTTTCAGCT[C/G]TGTCCTCACCTCCAC | 27342 |
| rs796507846 | multinucleotide-polymorphism | CA/TG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66784693 | CAGTGGACTTGTGTC[CA/TG]AATAATTTTTAGATA | 27342 |
| rs796518784 | in-del | -/AG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66796248 | TAGTTTAAAAAAAAA[-/AG]AGCTTCAAGTTTTTA | 27342 |
| rs796534188 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66741439 | GAGGAGAGCCGAGGG[A/G]TGCCCATCACGGCAG | 27342 |
| rs796537394 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66792012 | AGCTACTCGGGAGGC[C/T]GAGGCAGGAGAATTG | 27342 |
| rs796545633 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728765 | CGACCCTCACCGCCA[C/T]CCTCACCTCCACCCT | 27342 |
| rs796547295 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66734547 | GTGATCCGCCCATGT[C/T]GGCCTCCCAAAGTGC | 27342 |
| rs796554614 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699691 | GCAAAATTCCATCTC[-/A]AAAAAAAAAAAACAA | 27342 |
| rs796556666 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | RABGEF1, GTF2IRD1P1 | GRCh38.p7 | 7:66809703 | GTAAAGATAGAAATT[A/G]TATTGATAAGTAAAT | 27342 |
| rs796574315 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773937 | TCCCAGTGTGCTGGG[A/G]TTACAGGCGTGAGCC | 27342 |
| rs796575765 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728912 | CCTCCACGCTCACCT[G/T]CATCTTCACCTCCAT | 27342 |
| rs796610973 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66710692 | CTTTGGAGAAATGTC[C/T]GTTTAATTTTCCTCC | 27342 |
| rs796612963 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728659 | TCGACTTTCAGCTCT[A/G]TCCTCACCTCCACCT | 27342 |
| rs796626673 | snp | A/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728854 | TACACCTACACGTCT[A/T]TCCTCACCTCCACCT | 27342 |
| rs796656240 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728645 | TCATCATCCTCGCCT[C/T]GACTTTCAGCTCTGT | 27342 |
| rs796673174 | multinucleotide-polymorphism | AT/TC | | | intron-variant, nc-transcript-variant | RABGEF1, LOC107986707 | GRCh38.p7 | 7:66759724 | GTTTAAACAACCAGA[AT/TC]TCACAAGCACAGAAC | 27342 |
| rs796674058 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66726717 | TGGTCTAAAATGGAC[G/T]GCGAGGTCAGGTGCG | 27342 |
| rs796682722 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66716046 | CTTGAAGAGTCCAAC[C/T]ATAATTTTGAGTTTG | 27342 |
| rs796704478 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66732811 | TCTCGCTTTTGCTCT[C/T]GCTCTCACTCTGTAG | 27342 |
| rs796741641 | in-del | -/GT | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66773083 | TCTAGCTAGTTGTTT[-/GT]TTTTTTTTTTTCATC | 27342 |
| rs796781270 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66771433 | TGTGAGCCACCACAC[C/T]GGCCTGTGCAGACAT | 27342 |
| rs796785495 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66797306 | CAGACTCTTTGTTTG[A/C]AAAAAAAAAAAAAAA | 27342 |
| rs796817394 | in-del | -/TCATCCTCG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728633 | TCACCTCCATCCTCA[-/TCATCCTCG]CCTCGACTTTCAGCT | 27342 |
| rs796828550 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66699951 | GTCCCTGTCAGATGG[A/G]AACAGCAAATGTGGG | 27342 |
| rs796851408 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66791742 | ATAATGTTCAAAGAT[-/A]GACATCCACTTGTCA | 27342 |
| rs796854812 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66761570 | TGTCTGAAAGCTTCC[C/T]GGGCCCAGTTCTCTT | 27342 |
| rs796858654 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66806201 | AGGGGAAGCCAGGAT[A/G]CATTGCGAGTATTTC | 27342 |
| rs796863507 | in-del | -/GG | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66740870 | GGGGCGTCTCGGGCT[-/GG]GGGTGGCAGGGCGGT | 27342 |
| rs796879884 | snp | A/C | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728655 | CGCCTCGACTTTCAG[A/C]TCTGTCCTCACCTCC | 27342 |
| rs796893668 | in-del | -/AA | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66789707 | AAAAAAAAAAAAAAA[-/AA]GATGTATTTGATAAT | 27342 |
| rs796913381 | in-del | -/A | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66785880 | CTCCATCTGGGGGGG[-/A]AAAAAAAAAAGTCTT | 27342 |
| rs796924455 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66728871 | CCTCACCTCCACCTT[C/T]AACTCCACTCTCATC | 27342 |
| rs796939629 | snp | G/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66725208 | TATCAAGATACACTT[G/T]ACTTTACCATACAAT | 27342 |
| rs796944423 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729435 | CTCTGTCCTCCCGTC[C/T]ATTCTCCTCTCCAAC | 27342 |
| rs796982582 | snp | C/T | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66729498 | CATCCTCACCTCCAT[C/T]CTCACCTTCAACCTC | 27342 |
| rs797009802 | snp | A/G | | | intron-variant | RABGEF1 | GRCh38.p7 | 7:66715187 | GGCTGGAGTACCATG[A/G]CAGGATCCTAGCTCA | 27342 |
| rs797011670 | snp | A/G | | | intron-variant, upstream-variant-2KB | RABGEF1 | GRCh38.p7 | 7:66738678 | TGGAGGCTGGAGTGC[A/G]CCGAGATTGCACCAC | 27342 |