| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs372760746 | snp | C/G | 6.73446e-05 | 0.00580239 | intron-variant | RAB40C | GRCh38.p7 | 16:618310 | AAGGATGTTTCTCCT[C/G]ATTCTTTCTGAATGT | 57799 |
| rs372803676 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:620423 | CTGTGTGGGTGATTT[A/G]CATCTACAAAAATGC | 57799 |
| rs372810506 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:626291 | TGGTAAGAGCAGCCT[C/T]GGGGGAGAGGCGGCA | 57799 |
| rs372871673 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:606753 | CAGAGCCAGCACTGG[C/T]GGGTGAAGTCCCTCT | 57799 |
| rs372875265 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:618595 | TGCACTCAGGGCCAT[A/G]TGTGTGTGCAGCCAT | 57799 |
| rs372878573 | snp | C/T | 0.000297786 | 0.0121985 | synonymous-codon | RAB40C | GRCh38.p7 | 16:627511 | CTACTCCCTGGCCAG[C/T]GGGGCCGGGGGCGGC | 57799 |
| rs372881721 | snp | A/G | 0.000163975 | 0.0090532 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629671 | GTGTCTGCTATGCCC[A/G]GCCCAGGGGGGTGTG | 57799 |
| rs373035221 | in-del | -/A | | | intron-variant | RAB40C | GRCh38.p7 | 16:617861 | AAAGAAAAAAAAAAA[-/A]GCATTTCCCAGAACG | 57799 |
| rs373184120 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RAB40C | GRCh38.p7 | 16:625639 | CCCTGCACTGTCCCA[C/T]GGCCTACGCCTGGGC | 57799 |
| rs373191568 | snp | A/G | 0.000199002 | 0.00997302 | missense | RAB40C | GRCh38.p7 | 16:627524 | AGCGGGGCCGGGGGC[A/G]GCGGCAGCAAGGGCA | 57799 |
| rs373191734 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:610490 | GCTGACCTTCACTGG[C/T]GCCCTTGCCTTTTCA | 57799 |
| rs373285793 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:616029 | TTGGGAGGCTGAGGC[A/G]GGTGGATCATGAGGT | 57799 |
| rs373362352 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | RAB40C | GRCh38.p7 | 16:623383 | GGCCGGGCGCGGTGG[C/G]TCACGCCTGTCATCC | 57799 |
| rs373431594 | snp | C/G | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588176 | CACCCCCCGCTTCCA[C/G]GCAGTCTCAGAAACC | 57799 |
| rs373466504 | snp | C/T | 6.60971e-05 | 0.00574841 | synonymous-codon | RAB40C | GRCh38.p7 | 16:617251 | GCTGGACGGCCGGCG[C/T]GTGAAGCTGGAGCTC | 57799 |
| rs373626563 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | RAB40C | GRCh38.p7 | 16:607531 | ACGGGGGGCCGGGCG[C/T]GGTGGCTCACGCCTG | 57799 |
| rs373749522 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629398 | TTCCCTGCGCTGACC[A/G]GGCTGACCTGCCGCG | 57799 |
| rs373855017 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589484 | CTGCATCCTGCCGCC[C/T]GTCCGCGCGTTGAAG | 57799 |
| rs373858375 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:604690 | AATTGCTGTCATATA[C/T]GAGTGTACGTTTTAA | 57799 |
| rs373874310 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:626885 | GGAGGTTGCAGTGAG[A/C]GGAGATCGTGCCACG | 57799 |
| rs374064505 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RAB40C | GRCh38.p7 | 16:621451 | GCCATCTGCAAGACC[C/T]AGGCCGCGGGGACCT | 57799 |
| rs374183691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:613955 | CGCAGCTCGGGAAGC[A/G]CACAGTCGGCGCAGA | 57799 |
| rs374188422 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:591351 | CGAGGGAAGGTGTTA[G/T]AGATCTGGGGAAAGG | 57799 |
| rs374273325 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RAB40C | GRCh38.p7 | 16:623465 | CCATCCTGGCTAACA[C/T]GGTGAAACCCTGTCT | 57799 |
| rs374368525 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:600026 | TCAGCGTGGATTCGC[A/G]AGGTTTTGTTCCCTC | 57799 |
| rs374397085 | snp | A/G | 0.000198223 | 0.00995349 | intron-variant | RAB40C | GRCh38.p7 | 16:625867 | TGGGTGGCACCCTGC[A/G]TTTGTGCGTCTGCTG | 57799 |
| rs374410326 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593132 | GCGCTTTCTGTGTCT[A/C/G]AGGTCTCAAGGTTAA | 57799 |
| rs374493481 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | RAB40C | GRCh38.p7 | 16:618766 | ACGCACTGGGGCCAT[G/T]TGTGCAGTGTGTGCA | 57799 |
| rs374498344 | snp | C/T | 0.00146116 | 0.0269897 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629773 | GGCTCAGGTGCCTCC[C/T]TGTGCTGTTTCGTGG | 57799 |
| rs374509789 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:625716 | ACCAGGAGCTACGGG[A/G]CCACCCGGAAGGGCT | 57799 |
| rs374538321 | snp | C/T | 8.30144e-05 | 0.00644207 | intron-variant | RAB40C | GRCh38.p7 | 16:617188 | GGCGCGTCCCCTCAG[C/T]GCCCTGTGCTTCCTC | 57799 |
| rs374541279 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RAB40C | GRCh38.p7 | 16:624302 | AAATGAGCCAGCCCC[A/G]GTCCCTGTGCCCCAA | 57799 |
| rs374571388 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:616464 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAA | 57799 |
| rs374574255 | snp | C/T | 1.74127e-05 | 0.0029506 | intron-variant | RAB40C | GRCh38.p7 | 16:627323 | AGCCCCATGGTCTGA[C/T]ACCCCCTCTGCCCCA | 57799 |
| rs374602717 | snp | A/C/T | 1.671e-05 | 0.00289045 | synonymous-codon | RAB40C | GRCh38.p7 | 16:625503 | CTGGATCAAGGAGAT[A/C/T]GATGAGGTAGGCCTG | 57799 |
| rs374619569 | snp | A/G | 0.000234251 | 0.0108199 | intron-variant | RAB40C | GRCh38.p7 | 16:617158 | GCTGGTCTCGCGGGC[A/G]CTCGCTCCAGGAGTG | 57799 |
| rs374628014 | in-del | -/TTC | | | cds-indel | RAB40C | GRCh38.p7 | 16:628338 | CTGTGATGTGACACC[-/TTC]GGGGACATTGACCAC | 57799 |
| rs374631388 | snp | A/C/G | 0.000106147 | 0.00728454 | intron-variant | RAB40C | GRCh38.p7 | 16:627305 | CAGGGCCTCCTCCCC[A/C/G]ACAGCCCCATGGTCT | 57799 |
| rs374633425 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:611243 | TTGCAGCAGCCATGG[A/C]TCCTGGTGGCCCTGG | 57799 |
| rs374638301 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:590743 | GGGTCCGGGATCTGG[A/G]GCCCAGGGGAAGGTG | 57799 |
| rs374810504 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:623000 | TCCCTGCGGCCTCAC[C/T]GTGACCCACGCCGGA | 57799 |
| rs374920886 | snp | A/G | 0.000677656 | 0.0183948 | intron-variant | RAB40C | GRCh38.p7 | 16:626139 | GGGTGGGCGGGCGCC[A/G]GCCAGCCCTGAGGTC | 57799 |
| rs375060585 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:614492 | CTGCTAACTCTGCCG[C/T]ATCCCGATGGTGAAC | 57799 |
| rs375064358 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594799 | CTCCCCTGCACTTGA[C/T]TAGGTTTTGCTCGTC | 57799 |
| rs375219289 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:605537 | CTTGTCTAGTTTTCA[C/T]GTCAATGGAGCCACA | 57799 |
| rs375266072 | snp | C/T | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587431 | CTGGGCCTGCTGCCC[C/T]AGAGTCCGTCCCTCC | 57799 |
| rs375317511 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:607878 | GTCGCACCTAGTAAA[A/G]CAAACGCCTCAGTGA | 57799 |
| rs375325900 | snp | C/T | 6.07048e-05 | 0.00550897 | synonymous-codon, intron-variant | RAB40C | GRCh38.p7 | 16:625907 | CCCCCAGCATGCACC[C/T]GGAGTCCCCCGGATC | 57799 |
| rs375327956 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RAB40C | GRCh38.p7 | 16:619526 | GAAGCCCATGTAAAC[A/C]GACCTGTCATGGCCA | 57799 |
| rs375365561 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:623377 | ATGCTGGGCCGGGCG[C/T]GGTGGCTCACGCCTG | 57799 |
| rs375373231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:607530 | AACGGGGGGCCGGGC[A/G]CGGTGGCTCACGCCT | 57799 |
| rs375432438 | snp | A/G | 1.65269e-05 | 0.00287457 | intron-variant | RAB40C | GRCh38.p7 | 16:617284 | GTGAGTTGGGGCTGC[A/G]GCACTTCAGTTCCTG | 57799 |
| rs375484109 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:612669 | AAGAGCAGGGACAGC[C/T]GCCCTGGCCTGTAGC | 57799 |
| rs375569170 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:621708 | TGTGTGGAGGGTGGG[G/T]TAGGCTCCTTGTAAC | 57799 |
| rs375742416 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:613772 | GGAGTCGTGGGCAAC[A/G]CCCAGGTCTAGACCC | 57799 |
| rs375833821 | snp | C/T | 1.65729e-05 | 0.00287857 | synonymous-codon | RAB40C | GRCh38.p7 | 16:627517 | CCTGGCCAGCGGGGC[C/T]GGGGGCGGCGGCAGC | 57799 |
| rs375952497 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:592702 | GTGTTTGTGCATGTT[A/C]AGAAGAGCACGGGAA | 57799 |
| rs376007360 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:603702 | ATATATGTACCTATG[C/T]AGCCAGTACCCTCAT | 57799 |
| rs376035313 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:602639 | GGTTTCACCATGTCG[A/C/G]CCAGGCTGGTCTCGA | 57799 |
| rs376046748 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:610170 | CAGCAGCCGAGGCGC[C/T]GGTGGCTTTGCTCTG | 57799 |
| rs376056213 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:621224 | GCCGTGACTGAGCAT[C/T]TGGGCCACCCCGGGA | 57799 |
| rs376121179 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:619518 | AAGGACGTGAAGCCC[A/G]TGTAAACAGACCTGT | 57799 |
| rs376126601 | snp | C/T | 0.000149339 | 0.00863987 | synonymous-codon | RAB40C | GRCh38.p7 | 16:627526 | CGGGGCCGGGGGCGG[C/T]GGCAGCAAGGGCAAC | 57799 |
| rs376134347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:613927 | ACCACTGGGGCAGTG[A/G]CGCAGCTTCACACGC | 57799 |
| rs376219247 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:624948 | CCTGCTCTGCCTGGC[G/T]GGGGGAGCTTCACAG | 57799 |
| rs376408455 | snp | A/G | 0.0119091 | 0.0762411 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628678 | CAGGCACGCAGGGCC[A/G]GCCACCTCTCTCCTG | 57799 |
| rs376410585 | in-del | -/TTTA/TTTATTTA | | | intron-variant | RAB40C | GRCh38.p7 | 16:616333 | CCGGAGAAGCAGCAT[-/TTTA/TTTATTTA]TTTATTTATTTATTT | 57799 |
| rs376424371 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RAB40C | GRCh38.p7 | 16:618971 | GCCATGTGTGTGCAG[A/G]CATTTGCACAGGTCT | 57799 |
| rs376490054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:606618 | GCTCGTTGGGAGGTT[A/G]GCAGAATTCCGTTCT | 57799 |
| rs376555072 | snp | C/T | 4.95119e-05 | 0.00497529 | synonymous-codon | RAB40C | GRCh38.p7 | 16:627406 | CGTGCACCTCATCGA[C/T]AAGCTTCCACTGCCC | 57799 |
| rs376590801 | snp | C/T | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589114 | CCGCAGTGAGCACGT[C/T]GGGCCGGGTCTTGAG | 57799 |
| rs376596003 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:616040 | AGGCGGGTGGATCAT[A/G]AGGTCAGGAGATCGA | 57799 |
| rs376659048 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:603746 | ACATCCACTCTCCTC[C/T]CAGAAAGCCCCTCAG | 57799 |
| rs376677697 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:621940 | GGATGTGAGTGGGCG[C/T]GGCTTGGCAGTAGCT | 57799 |
| rs376689730 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594207 | CAGGGTGTGTGTGCC[C/T]GGGTCCTGGAAGACT | 57799 |
| rs376694286 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:601935 | GATTGGGACCATCCT[G/T]GCCAGCATGGTGAAA | 57799 |
| rs376751567 | snp | C/G/T | 3.32027e-05 | 0.00407434 | synonymous-codon | RAB40C | GRCh38.p7 | 16:626081 | ATCCCGCATCGTGCT[C/G/T]ATGCGGCACGGCATG | 57799 |
| rs376984115 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:621387 | ACTGTCTGTCCCAGC[C/T]GGGATTTGTCACTCT | 57799 |
| rs377013188 | snp | C/G/T | 3.39566e-05 | 0.00412036 | intron-variant | RAB40C | GRCh38.p7 | 16:625530 | CCTGGGTCCGGGGAG[C/G/T]CCTCCCGGGGAAGGC | 57799 |
| rs377033079 | snp | G/T | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593097 | CGAGCAGAGAAGGAA[G/T]CGCCTCTGGGCTGTG | 57799 |
| rs377047571 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:618843 | CACTCGGCCATGTGT[A/G]TGTGCAGGCATGTGC | 57799 |
| rs377175531 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:609476 | AAAAGAAGCGGCCAC[A/G]AGACGCCGCCGAGAG | 57799 |
| rs377224353 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:603662 | TGTACCCTCTTTGCA[C/T]GTACAGTTCTATGAG | 57799 |
| rs377230835 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:615549 | TTCTGGAAAGTTTCC[A/C]GAGGGCCCAGAGCCT | 57799 |
| rs377285042 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629095 | GGCCCCACCTGTCCT[A/G]TTGCTGCCAGCAGGG | 57799 |
| rs377386232 | in-del | -/A | 0.5 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:611972 | TGTAGAATCAAGAGC[-/A]AGGGACAGCCGCCCT | 57799 |
| rs377428149 | snp | C/T | 1.6638e-05 | 0.00288422 | synonymous-codon | RAB40C | GRCh38.p7 | 16:618236 | GTTCTGCACCATCTT[C/T]AGGTCCTACTCCAGG | 57799 |
| rs377462268 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:603733 | CCAAATCAGGAGCAC[A/G]TCCACTCTCCTCCCA | 57799 |
| rs377548948 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:626356 | CCTCAGGGTGCCGCC[A/G]TGGCCGCTGCACTCT | 57799 |
| rs377573986 | in-del | -/A | | | intron-variant | RAB40C | GRCh38.p7 | 16:613108 | TGTAGAATCAAGAGC[-/A]AGGGACAGCCGCCCT | 57799 |
| rs377619244 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:615818 | ATTATAAAAATTAGC[C/T]GGCTGTGGTGGTGGG | 57799 |
| rs377620108 | snp | C/T | | | synonymous-codon, intron-variant | RAB40C | GRCh38.p7 | 16:625922 | CGGAGTCCCCCGGAT[C/T]TTGGTTGGAAACCGG | 57799 |
| rs377620784 | snp | A/G | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596557 | GTGTCGGCGTCCAGC[A/G]TCCTGGTGCGGAGAA | 57799 |
| rs377741889 | snp | C/T | 0.000305816 | 0.0123618 | intron-variant | RAB40C | GRCh38.p7 | 16:625863 | GGGGTGGGTGGCACC[C/T]TGCGTTTGTGCGTCT | 57799 |
| rs377743317 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:608813 | AGAAGGTGGAGGTTG[C/T]CATGAGCCAAGATTG | 57799 |
| rs377743781 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587536 | AGGGCACAGCAGCTT[G/T]CCAAGGATCTCACCC | 57799 |
| rs377750685 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:600295 | CTCCTGGTGGGGAGG[A/G]ATAGCTAGTATGTCA | 57799 |
| rs386787582 | multinucleotide-polymorphism | CGT/TGG | | | intron-variant | RAB40C | GRCh38.p7 | 16:601113 | TCACCGTTCAGTAAA[CGT/TGG]GCCTGCTGCTTGTGT | 57799 |
| rs386787583 | in-del | CG/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:614178 | CCGATGGTGAACTGC[CG/T]AACTCTACCGCATCC | 57799 |
| rs386787584 | multinucleotide-polymorphism | CAC/GAT | | | cds-indel | RAB40C | GRCh38.p7 | 16:628841 | GCACGACATGGCCAG[CAC/GAT]GCAGAAGGAGCCCTC | 57799 |
| rs397736782 | in-del | -/A | | | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:597964 | AAAAAAAAAAAAAAA[-/A]GGCCGGGTGCAGTGG | 57799 |
| rs397855977 | in-del | -/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:604249 | TTAAATTTTTTTTTT[-/T]AATTATTTTTCTTGT | 57799 |
| rs398028564 | in-del | -/A | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:602261 | AAAAAAAACAAAACC[-/A]AAAAAAAAAAAAACA | 57799 |
| rs398028565 | in-del | -/C | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:617630 | GTCTTGGACTCCTGA[-/C]CTCAGGTGATCCTCC | 57799 |
| rs398042015 | in-del | -/T | 0.5 | 0 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587821 | TTTTTTTTTTTTTTT[-/T]CCTGAGACAAGAGTC | 57799 |
| rs527240132 | snp | C/T | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:604797 | GGGTGTGGTGGCTCA[C/T]GCCTGTAGTCTCAGC | 57799 |
| rs527332033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629348 | TGCTGCTTCATACCC[A/G]GCAAACTGACCTCTG | 57799 |
| rs527467607 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595379 | CCGCCCTGCAGGCCT[C/T]CTGTGAAGCAGCGGG | 57799 |
| rs527473349 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:625106 | TTAGCTTCCACAGCT[C/G]CACGTCCCCCGGCTG | 57799 |
| rs527532398 | snp | C/T | 0.000164082 | 0.00905617 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629694 | GGGGTGTGGACGCCC[C/T]GGAGGTCACAGCTGA | 57799 |
| rs527582980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:591067 | CATAGATCTGGGGGA[A/G]GGCATCATGGTCCTA | 57799 |
| rs527600536 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | RAB40C | GRCh38.p7 | 16:601214 | TACCAAAAACTATGA[-/T]TTTTTTGTGTGTTAT | 57799 |
| rs527602322 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:590595 | TGGCTGCGGGGTGCC[C/G]GTGCTCCAGTCCCGA | 57799 |
| rs527840174 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:606457 | CTCGGTCCTCAGTCC[A/G]GTGTGGGTTTCCCTG | 57799 |
| rs527846462 | snp | C/T | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:600792 | TGCCTACGTGCGTCA[C/T]ACAGACAGTTTAACA | 57799 |
| rs527973186 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596520 | GTGTCATCCGCCGGG[C/T]GTTTGGAGTAAGCAG | 57799 |
| rs528072095 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RAB40C | GRCh38.p7 | 16:590516 | GCCCTCGGCCCGGCC[C/T]TTCCAAGCGCCGCCG | 57799 |
| rs528080938 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:617982 | CTTGCTCACTCCCCA[C/G]GTGGGCGGGGGCCCC | 57799 |
| rs528145776 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:592602 | GACTCAGGTGGTGGG[C/T]GGCCAAGTTGATTGT | 57799 |
| rs528226355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:608287 | CACAAAAACAGCAGG[A/G]GGGAACCACCCCCAT | 57799 |
| rs528256012 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:602947 | TCATTGAAAGTAATC[G/T]GAGAGCTATGGGATC | 57799 |
| rs528287177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:614400 | GAACTGCCTAAACCT[C/T]GTCCCGATGGTGAAC | 57799 |
| rs528380532 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RAB40C | GRCh38.p7 | 16:598873 | GTGAAGGTGTAGGCC[A/G]GGCGGTCAAGCACAG | 57799 |
| rs528451113 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628652 | ACCAGCCCGGCGCTC[A/G]TGCTGAGCCCCAGGC | 57799 |
| rs528468891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:599184 | AGGGGAGGGGAGTAT[A/G]GTCACAGCCCAGGCC | 57799 |
| rs528526762 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628192 | GCCCTGGCTCCCACG[A/G]GATGGAGGGTGTGGT | 57799 |
| rs528558582 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:623992 | TCTTACCTCACCTGG[G/T]TTGCACATCTCTCCT | 57799 |
| rs528606705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595424 | CCCTGTCCTCCTCAC[A/G]TCCACCTGGGCCTGG | 57799 |
| rs528658751 | in-del | -/TC | 0.00398564 | 0.0444627 | intron-variant | RAB40C | GRCh38.p7 | 16:621258 | CAGCCCTGTCCTGTG[-/TC]TCTCCTGCCTGGTGA | 57799 |
| rs528678891 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:615088 | TAAAATTGGGACGTT[G/T]GGTTTTCTGTTGTTG | 57799 |
| rs528689781 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:620198 | AAGAGTTGGAGACCA[A/T]CCTGACCAACATGGT | 57799 |
| rs528812899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:615614 | ACTGTCTGCTCCTTT[C/T]AGTTTCTCTTGGACT | 57799 |
| rs528817558 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RAB40C | GRCh38.p7 | 16:614429 | ACTGCCTAACTCTAC[C/T]GCATCCCGATGGTGA | 57799 |
| rs528880172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:619189 | GCACAGGTGTAGTGG[A/G]TGCACTCAGGGCCAT | 57799 |
| rs528911304 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:625006 | GCTCTGCAAGTTTTA[C/G]GTTGGAAAACTCAGA | 57799 |
| rs528963079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:608935 | GCCTGGGCAACACAG[C/T]GAGACCCCTGACTGT | 57799 |
| rs528965504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:603845 | AGACATCATGGATAC[A/G]AAGCAGACCCTGGTT | 57799 |
| rs528967258 | snp | A/C | 0.00027342 | 0.0116891 | intron-variant | RAB40C | GRCh38.p7 | 16:627337 | ACACCCCCTCTGCCC[A/C]ACAGTGTTCAGCCTG | 57799 |
| rs528994303 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:626548 | CTCCCGTGAAGCCCC[A/C]CTCAGGGAGGTGGTA | 57799 |
| rs529126205 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628700 | TCTCTCCTGAAGCCA[C/T]TGGCCGCTCCTCCAC | 57799 |
| rs529166874 | snp | A/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:591819 | CCAGGATGGTCTCAA[A/T]CTCCTGACCTCATGA | 57799 |
| rs529247988 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:599211 | GGCCCCGGCCCCGGC[C/T]GAAGCTGCCACTGAC | 57799 |
| rs529257681 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589446 | TTCCCGGACTCAGCC[A/G]CATCGCCTCGGCTCG | 57799 |
| rs529261613 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629180 | TGCATTCACGGCATC[A/G]ACACTACCCGCGCTG | 57799 |
| rs529282970 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:619883 | TGATGTCTTCTACCT[C/G]CTGGCGGTGGGTGGG | 57799 |
| rs529300062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:624022 | TTGGCCAGCATGCAC[A/G]CTTTTACATGCACTG | 57799 |
| rs529377739 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | RAB40C | GRCh38.p7 | 16:590224 | GCGGGGCGCGGGCTC[A/T]CTCACGCCGCGGCCT | 57799 |
| rs529400224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:620265 | GAGCATGGTGGCGGG[C/T]GCTTATAATCCCAGC | 57799 |
| rs529468169 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:616056 | AGGTCAGGAGATCGA[C/G]ACCATCCTGGCTAAC | 57799 |
| rs529468238 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:609814 | AACTGGGCAGTCCCT[A/G]CAGAGGTCACCCTGG | 57799 |
| rs529638944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:604917 | ATACAAAGTTAGCCT[A/G]GTGTGGTGGTGGTGC | 57799 |
| rs529658193 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:610208 | GACAGGTGTTCTGAC[C/G]TCCCTGCCTCTGTCC | 57799 |
| rs529709453 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:621972 | CCATTTTACATGTCA[G/T]TTGCTCCTGGGCAGA | 57799 |
| rs529737631 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:604214 | CATGTACCACCACAC[C/G]CGGCTCAGAGCTAGT | 57799 |
| rs529780659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622386 | GACCCCGCCCGCGAG[A/G]CATGAGCGGCACCGT | 57799 |
| rs529842007 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:613319 | AAGAGCAGGGACAGC[C/T]GCCCTCGCCTGTAGA | 57799 |
| rs529993918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:602368 | CTAGTGATCCTCCCG[C/T]CTCAGCCTCTCAAGT | 57799 |
| rs530095284 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:622721 | ATGTTGGCCAGGATG[A/G]TCTCCATCTCTTGAC | 57799 |
| rs530111326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:627199 | CAGAGAAGTTTGGGC[A/G]TCCAGGTCCTCCAGG | 57799 |
| rs530118768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:598074 | ACATGATGAAACCCC[A/G]TCTCTACTAAAAATA | 57799 |
| rs530121525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:592867 | CTCCCTGTCCCCTTC[A/G]TCGGGCTGTGGGGCA | 57799 |
| rs530173674 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:601638 | AATTGTTATCCTAAA[A/G]TTACATGAGAGGGAA | 57799 |
| rs530177213 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597820 | GGAAAAGAGCAGAGG[G/T]CTGGGCACGGTGGCT | 57799 |
| rs530180296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:602677 | ACCTCAAGTGATCCA[C/T]CCACCTCGGCCTCCC | 57799 |
| rs530359427 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:618563 | TTGGAGCTGTGTGTG[C/T]GCACAGGTGTAGTGG | 57799 |
| rs530362631 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RAB40C | GRCh38.p7 | 16:623376 | CATGCTGGGCCGGGC[A/G]CGGTGGCTCACGCCT | 57799 |
| rs530382845 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RAB40C | GRCh38.p7 | 16:601725 | GCACGCCTATAATCC[C/T]AGCTACTTGGGAAGT | 57799 |
| rs530421014 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | RAB40C | GRCh38.p7 | 16:620133 | GGTGCGGTGGTTCAC[G/T]CCTGTAATCCCAGCA | 57799 |
| rs530430076 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588046 | CCTCAGGTGATCCAC[C/G]CACCTCAGCCTCCCA | 57799 |
| rs530434956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622468 | GGGCCTAGAGCAGGG[C/T]GAGCGCGCGTCCTGA | 57799 |
| rs530512739 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:610237 | CCCCTGAGGTCAGAG[C/T]GCCTGTCCTGTGGAG | 57799 |
| rs530550160 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:592713 | TGTTCAGAAGAGCAC[A/G]GGAAGGATTGGGTTT | 57799 |
| rs530591455 | snp | C/T | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587394 | ACTGGGCCTGCTGCC[C/T]CAGAGTCCGTCCCTC | 57799 |
| rs530641798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:618395 | CACATTGGTTTGTTT[A/G]TTTGTTTGTTTTGAG | 57799 |
| rs530646819 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587579 | CCTGAACCCAGGAAC[C/T]CAGGACAGGGCTGTG | 57799 |
| rs530667758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:617873 | AAAAGCATTTCCCAG[A/G]ACGTCAGCGTTGATG | 57799 |
| rs530683898 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RAB40C | GRCh38.p7 | 16:614042 | CTAACTCTACCGCGT[C/T]CCGATGGTGAACTGC | 57799 |
| rs530685505 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:607556 | CGCCTGTAATCGCAG[A/C]ACTTTGGGAGGCCTA | 57799 |
| rs530748893 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:613672 | CCTTTGCCCTTTTTT[A/T]AAAGTATAATTTCCG | 57799 |
| rs530752290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:602456 | TTTATTTTTGAGACA[A/G]AGTCTTGCTCTTGTC | 57799 |
| rs530796385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:621413 | ACTCTGCCTCCCTCC[A/G]TTAGAGAGTGGAGAG | 57799 |
| rs530873404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:607812 | GAAAAGAAAAGAAAA[A/G]AAAGTCGCATCTGGT | 57799 |
| rs530899714 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:598209 | ATGGTGAAACCCTGT[A/C]TCTATAAAAATACAA | 57799 |
| rs530905279 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593964 | CGGCGGGGAGGAGAA[A/G]GCTGCAGTTCAGGAG | 57799 |
| rs530912701 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:598826 | TACAGTTTGTACAGC[A/G]GCCGGATGTAAGAAC | 57799 |
| rs530988459 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:617335 | AGGGAGAACAGAACC[C/T]TTAGAGAAACAGGAA | 57799 |
| rs530997436 | snp | G/T | 0.0111196 | 0.0737302 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628116 | TGCGAGTGGCGGGGC[G/T]GCCCAGAGGCCGGGG | 57799 |
| rs531041206 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588756 | CGGGCTCCGCACCCG[C/G]TCTGGAGAGGGCTGC | 57799 |
| rs531123149 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:623948 | TTCAAAAAAAAAGAA[A/T]ATGCCATCCGCAGTG | 57799 |
| rs531128745 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589234 | GAACCTCAGCGACTT[G/T]GCAGACTCACTGGTG | 57799 |
| rs531131033 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:619214 | GGCCATGTGTGTGTG[C/T]AGGCATGTGCACAGG | 57799 |
| rs531144246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:614529 | ACTTTACCTCGTCCC[A/G]ATGGTGAACTGCCTA | 57799 |
| rs531145013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:619769 | GTCCGCTCTGGGCAG[A/G]AAGCTGCCCAGGTGC | 57799 |
| rs531176693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:600223 | ACAGTCTGTACTTCC[A/G]GCAGATGTGGGTCCT | 57799 |
| rs531248304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596931 | AGTGCGCGGCTGTCT[C/T]GTGCTGAGATCAGGA | 57799 |
| rs531432665 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:591130 | GGTCCGAGGGAAGGT[A/G]TCATAGATCTGGGGA | 57799 |
| rs531442817 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594962 | GTAGCTGGGATTACA[A/G]ACGCCTGCCACCATG | 57799 |
| rs531536863 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:616634 | TGAGCCACCGCGCCC[A/G]GCCAGAAGCAGCATT | 57799 |
| rs531556176 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:611574 | CTCCCTGAAGAGTGT[C/T]GTTTCACTTGTGAGT | 57799 |
| rs531616420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:617010 | GCCCTGCCCGTGGCC[C/T]GTGTGCAGAAGTGGG | 57799 |
| rs531619329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:611192 | CTGTGGGTGGGTGAC[A/G]TGGTCCCCAGGCTTT | 57799 |
| rs531637659 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:599274 | TGCTCCGAGGGGTGT[C/T]TGTGTCCTCAGGCTC | 57799 |
| rs531737031 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:613194 | GGACAGCCGCCCTCA[C/T]CTGTAGAATCAGCAG | 57799 |
| rs531757843 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RAB40C | GRCh38.p7 | 16:606510 | GACACACAGTCCTCT[C/T]GGTCCTCAGTCCAGT | 57799 |
| rs531815909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:606984 | CTGCTGGTGGCAGGC[C/T]GGCCCAGACAGACAG | 57799 |
| rs531908949 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596564 | CGTCCAGCATCCTGG[G/T]GCGGAGAACGCTGCC | 57799 |
| rs531967509 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:624968 | GAGCTTCACAGAAAC[-/T]GTCCTGGAGGGACTG | 57799 |
| rs532035861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:592096 | TGGGAGCAGTCAGCA[C/T]CCAGCCTCCCCAGAG | 57799 |
| rs532096058 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:601193 | TTTGACTTTTAAAAA[A/G]TTGTAGTACCAAAAA | 57799 |
| rs532136994 | snp | A/G | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594503 | CTTCTTCGGCTTCAC[A/G]ACTCCCTGAGCTTTC | 57799 |
| rs532196596 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:617110 | CTTCTCCACTTCCGC[A/G]TGGGTCTTGGCCCTG | 57799 |
| rs532235428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596473 | CACCCCACCGAGGGC[C/T]GTTCTGGGGCCCAGG | 57799 |
| rs532324119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:607057 | GTCCCACTTCCGAGC[C/T]GAGGGTGCTACGCAG | 57799 |
| rs532335702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622380 | CCCCTTGACCCCGCC[C/T]GCGAGGCATGAGCGG | 57799 |
| rs532435239 | snp | C/T | | | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:598076 | ATGATGAAACCCCGT[C/T]TCTACTAAAAATACA | 57799 |
| rs532487043 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597026 | TGGCGCTGTGGAGAG[G/T]TAGGGACCCATGGGT | 57799 |
| rs532551579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:613241 | CTGTAGCATCAAGAG[C/T]AGGGACAGCCGCCCT | 57799 |
| rs532583164 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:598072 | CAACATGATGAAACC[C/T]CGTCTCTACTAAAAA | 57799 |
| rs532635690 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622708 | ACGGGGTTTCACCAT[C/G]TTGGCCAGGATGGTC | 57799 |
| rs532648475 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:599642 | CCTCGTGGCATTAAT[C/G]AGCGTGGATTCAGCA | 57799 |
| rs532662707 | snp | C/T | 3.72079e-05 | 0.00431307 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627623 | TGCAAGATCTCCTAG[C/T]GGGGATGGGCGGGGC | 57799 |
| rs532685059 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593152 | CTCAAGGTTAAGACG[G/T]GCACAGCACAAGGAG | 57799 |
| rs532687665 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:604620 | GGTGTTTCTCTAGAA[C/T]ATATGTGAGTCTTTC | 57799 |
| rs532728767 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:609022 | CAGGAGGCTGAGCTA[C/T]GAGGAGCACGTGAGC | 57799 |
| rs532834409 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:607683 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 57799 |
| rs532841288 | snp | C/G | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587943 | CTCCTAAGTAGCTGG[C/G]ATTACAGGCACGTAC | 57799 |
| rs532851363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:592800 | ATGCTGGCCAGCTCG[C/T]CTACCCAACTGCACC | 57799 |
| rs533024684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629635 | CCGCTCAGCAGAGCC[A/G]CCTGCACGCTGGCCA | 57799 |
| rs533078903 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594861 | GTCTTACTCTCTTGC[A/G]CAGGCTGGAGTGCAG | 57799 |
| rs533245822 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595305 | CCCCCACTGTGCAGA[C/T]GAGGGATTGAGGCTC | 57799 |
| rs533251687 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | RAB40C | GRCh38.p7 | 16:590258 | CCGGCGGTGCTTCGG[A/C/T]AGGCGGCCGGCGCGG | 57799 |
| rs533364315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:620341 | GAGGTTGCAGTGAGC[C/T]GAGATTGTGCCATTG | 57799 |
| rs533391327 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:590567 | TGCCTGGCTTCCAGA[C/G]TCGGTAGCTCGGTGG | 57799 |
| rs533516004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:605406 | TTTAAAGTCTGCAAT[A/G]CAGTGAGTGCGGACA | 57799 |
| rs533526548 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RAB40C | GRCh38.p7 | 16:611109 | TGGGTGGGACGCAGA[C/T]GTCCAGCGGGAGGAG | 57799 |
| rs533559420 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:604406 | TCTGAAGGTGTTTCT[C/G]TAGAATACACGAGTC | 57799 |
| rs533563539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:599002 | CTTCCTGGTCAGCAA[C/T]GTTGTCGGCCACCTG | 57799 |
| rs533614882 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:624076 | GTACATTTCACTGCC[A/G]CTTACTCAGCTGTCC | 57799 |
| rs533633339 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589744 | CAATGGTTCCGGGAA[A/T]GCAGGAGGCGAGTGG | 57799 |
| rs533670650 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:592866 | CCTCCCTGTCCCCTT[C/G]GTCGGGCTGTGGGGC | 57799 |
| rs533803429 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:615872 | GAGGCTGAGGCAGGA[A/G]AATCGCTTGAACCCG | 57799 |
| rs533829590 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:618460 | AGTGGCACAGTCTCG[G/T]CTCACTGCAGCCTCC | 57799 |
| rs533919995 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:620288 | ATCCCAGCTACTTAG[A/G]AGGCTGAGGCAGGAG | 57799 |
| rs533955945 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:598781 | GATGGAAGAAGAGAA[G/T]AGCTGAGTCCTGGAA | 57799 |
| rs533988063 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:615405 | TGGGCAGGTGCACTC[C/T]GTGGGAGGGCGTCGC | 57799 |
| rs534178210 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:605113 | TGTAATAGTCTTAGC[G/T]ACTCAGGAGGCTGAG | 57799 |
| rs534269888 | snp | A/G | 0.000934143 | 0.0215916 | intron-variant | RAB40C | GRCh38.p7 | 16:625110 | CTTCCACAGCTGCAC[A/G]TCCCCCGGCTGCCAG | 57799 |
| rs534313199 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:613762 | GGTCTTAGTGGGAGT[C/G]GTGGGCAACACCCAG | 57799 |
| rs534319087 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | RAB40C | GRCh38.p7 | 16:599739 | TCAGCGTGGATTCGC[A/C]AGGTTTTGTTCCCTC | 57799 |
| rs534464118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:621280 | TGCCTGGTGAGCAGC[A/G]GTGAGGTGCGGGTGC | 57799 |
| rs534488956 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:591187 | GGGAAGGTGTCATGG[A/G]CCTAAGGGAAGGTGT | 57799 |
| rs534566973 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627778 | CCGGGTGCGAGGAGG[A/G]GCATGCACGGACCAA | 57799 |
| rs534591299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:607189 | CCCAGACCACCAGCA[C/T]GTTGATGACTGTTGA | 57799 |
| rs534591954 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587852 | TCACTCTGTAGCCCA[A/G]GCTGGAGTGCAGTGG | 57799 |
| rs534657648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:598278 | AGCTACTTGGGAGGC[C/T]GAGGTACGAGAATGG | 57799 |
| rs534672109 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588239 | GTCCCTGGAGTGAGG[A/G]GCCTCAGGGACTTCA | 57799 |
| rs534679533 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:591616 | TTTTTTTTTTGAGAC[A/G]GAGTCTCACTCTGTC | 57799 |
| rs534735445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:607651 | AAAAAATTAGGCAGG[C/T]GCGGTGGTGGGCGCC | 57799 |
| rs534759153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:624611 | CTCTTCTTTCAGCCT[C/T]AGCCTCTTGTGTGAT | 57799 |
| rs534834140 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:602473 | GTCTTGCTCTTGTCC[A/C]CCAGGCTGGAGTGTG | 57799 |
| rs534896999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:608381 | GCGGGGACACAGCCA[A/G]ATCTTATCACTCCTG | 57799 |
| rs534897170 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:608171 | ATTTACAGTCATGGC[A/G]GAAGGTACCTCACAC | 57799 |
| rs534912568 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RAB40C | GRCh38.p7 | 16:614578 | AACTGCCTAACTCTA[C/T]CGCATCCCGATGGTG | 57799 |
| rs534995963 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | RAB40C | GRCh38.p7 | 16:618837 | TGGGTGCACTCGGCC[A/T]TGTGTATGTGCAGGC | 57799 |
| rs535057977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:623158 | CACAGCACACTTGGA[A/G]CCTGAGGCAGCCCAT | 57799 |
| rs535083486 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:614240 | CGATGGTGAACTGCC[G/T]AACTCTACCTCGTCC | 57799 |
| rs535226746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:608047 | CCTCCACGCCCATGT[A/G]CTCACCTGTTCTCAC | 57799 |
| rs535275987 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628372 | CAAAACTCAGATCAT[C/G]TCGCCCACCCTGGAG | 57799 |
| rs535355883 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:623469 | CCTGGCTAACACGGT[A/G]AAACCCTGTCTCTAC | 57799 |
| rs535384646 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:602575 | CTGGGATTACAGGCA[C/T]CTGCCACCACGCCCG | 57799 |
| rs535453455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:607723 | ATGAACCCAGAAGGC[A/G]GAGCTTGCAGTGAGC | 57799 |
| rs535584846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:598023 | AGGCCAAGGTGGGTG[A/G]ATCACGAGGTCAAGA | 57799 |
| rs535610834 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593572 | GATCGCTTACCTGCC[G/T]GGAAGTCTTGTCTGG | 57799 |
| rs535620437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:623178 | AGGCAGCCCATCAGC[C/T]GGGAGGCGGGCCTTC | 57799 |
| rs535632837 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RAB40C | GRCh38.p7 | 16:604447 | TGTTTCTCTAGAATA[C/T]ATGTGAGTCCTTCTG | 57799 |
| rs535690593 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RAB40C | GRCh38.p7 | 16:609242 | TGAGGGGAAGGGGAG[C/G]TCAGGGCAGTGCCTG | 57799 |
| rs535720962 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:618870 | GTGCACAGGTCTGGC[A/G]GGGGCACTGGGGCCA | 57799 |
| rs535727564 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594592 | CCAATTCCAGGGGAC[A/G/T]CTATCTTGAGAGGCT | 57799 |
| rs535729887 | in-del | -/A | | | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:598378 | CGAGACTCCACCTCA[-/A]AAAAAAAAAAAAATA | 57799 |
| rs535745969 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588288 | GGGCACAATGACCTC[G/T]GAGCAGAAGAGGCTC | 57799 |
| rs535753413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594135 | AGGCAGTTCCACCCT[C/T]GGCACCGTGTCCCCA | 57799 |
| rs535786875 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:599392 | CCTGCCTGAGAGGAG[C/G]CGCCAGGTCAGCTGA | 57799 |
| rs535848883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:614673 | TGCCAAACTTTACCT[C/T]GTCCCGATGGTGAAC | 57799 |
| rs535862993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:619410 | AGGTATGGTGGGTGC[A/G]CTTGGCCACCCTCGT | 57799 |
| rs535979717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:608514 | ATCTGTGGCCCTCAG[C/T]GCCATCAGACCCAGG | 57799 |
| rs535986652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:615237 | AGAACAGCCTTTGAT[A/G]TACATGTAGGGGTTG | 57799 |
| rs536068619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:604215 | ATGTACCACCACACC[C/T]GGCTCAGAGCTAGTT | 57799 |
| rs536111148 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:610668 | CCCTGCCCCTGCGCC[A/G]TCCCCCAGCGCGGGC | 57799 |
| rs536189743 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:601495 | TGGGTGCCAGACTCC[A/G]GGCAGGTCCCCGCCG | 57799 |
| rs536202206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597146 | GGAGGGGCTCAGGAG[C/T]AGCCAGGTTCTAGTG | 57799 |
| rs536219370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:591731 | CGAGTAGCTGGGACT[A/G]CAGGTGTATGCCACC | 57799 |
| rs536250196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:616744 | GCCTTGGAGAATTCA[A/G]CTTCAAAATGCATAC | 57799 |
| rs536294315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:626338 | GAGCAGCTGATGACC[C/T]CCCCTCAGGGTGCCG | 57799 |
| rs536385113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:617152 | GCCGAGGCTGGTCTC[A/G]CGGGCGCTCGCTCCA | 57799 |
| rs536416071 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587721 | CTGGGTCTGGAGAGC[A/G]TTTTACTTTGTTTTT | 57799 |
| rs536442209 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:618034 | GCGGCACGGCGCCAG[A/G]CTGCTGTGACCTGTG | 57799 |
| rs536454719 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622746 | CTTGACCTCGTGATC[C/G]GCCTGCCTCGGCCTC | 57799 |
| rs536456704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:617580 | GGGTGTGGTGGCTCA[C/T]GCCTGTCATCCCAGC | 57799 |
| rs536465868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:611905 | TAGAATCAAGAGCAC[A/G]GGACAGCCGCCCTGG | 57799 |
| rs536466361 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:617848 | ACTCCGTCTCAAAAA[A/C]GAAAAAAAAAAAAGC | 57799 |
| rs536581376 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:613837 | GTCGTGGGCAGCACC[C/G]AGGTCTAGACTTGGG | 57799 |
| rs536629077 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589134 | CGGGTCTTGAGCTCG[C/T]GCCGGCCGCGCTCCC | 57799 |
| rs536637728 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:626812 | GCGTGGTGACGCACA[C/T]CTGTAGTCCCAGCTA | 57799 |
| rs536655116 | in-del | -/AA | | | intron-variant | RAB40C | GRCh38.p7 | 16:607503 | GTGAAACTGTCTCAA[-/AA]AAAAAAAAAAAAACG | 57799 |
| rs536866748 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:601515 | GGTCCCCGCCGCAGC[C/T]GCGTCAGCAGAGCAA | 57799 |
| rs536922676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:592308 | TCTCAACTCGGGGGT[C/T]GGCAGAGCGTGGGAT | 57799 |
| rs537010102 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:592979 | TCAGAGGCTCACAGT[A/G]GCTTGGACCAGAGGC | 57799 |
| rs537089187 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622523 | TTCTTTTGTTTTGTT[G/T]TTTGAGACACGGTCT | 57799 |
| rs537109534 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RAB40C | GRCh38.p7 | 16:590949 | TGTCATGGGTCCAGG[A/G]TCTGGGGTCCGGGGA | 57799 |
| rs537149452 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587786 | AAGAACATTTTTAAT[A/T]GTTTATTTTTGAGGC | 57799 |
| rs537179483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:606705 | GCTTCTCCAGGCCGC[C/T]TGCGTTGTTCACGGA | 57799 |
| rs537179703 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:613370 | GCCCTCGTCTTTAGA[A/T]TGAAGAGCAGGGACT | 57799 |
| rs537201371 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:601985 | ATAAAAGTTAGCGGG[G/T]TGTGGTGTCGGGCAC | 57799 |
| rs537234880 | snp | C/G/T | 0.00279242 | 0.0372774 | intron-variant | RAB40C | GRCh38.p7 | 16:607745 | GCAGTGAGCCGAGAT[C/G/T]GCGCCACTGCACTCC | 57799 |
| rs537250114 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:618711 | TGTAGTGGGTGCACT[C/G]AGGGCCATGTGTGTG | 57799 |
| rs537266973 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:607171 | CAGGTGCCACGTCCA[C/G]TCCCCAGACCACCAG | 57799 |
| rs537296898 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:626907 | CGTGCCACGGCACTC[C/T]AGCCTGGCGACAGAG | 57799 |
| rs537363073 | in-del | -/G | 0.0142736 | 0.0832652 | intron-variant | RAB40C | GRCh38.p7 | 16:610122 | TCTCCTGTAGCTGGT[-/G]GGGGAAGCGGCACCC | 57799 |
| rs537391986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597316 | GGAAACAGAAGCACT[C/T]GGCCCCTGAGCAGCC | 57799 |
| rs537469531 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:611065 | GTTCTGACGCGCACC[C/G]TGGGCAACCGGGTGC | 57799 |
| rs537484537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:627281 | TTGGGCACCTCAGGT[C/T]TCCCTGCACAGGGCC | 57799 |
| rs537549146 | snp | C/T | 1.96918e-05 | 0.00313776 | synonymous-codon | RAB40C | GRCh38.p7 | 16:590414 | CGGCGCGGCAGAGTC[C/T]CCGTACGCCTACAGT | 57799 |
| rs537599956 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:602288 | TTTTTATTAGAGAGA[C/T]AGTTTCACTCTTCCA | 57799 |
| rs537647986 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:609917 | TCCAGACTGCAAGGG[C/T]CACAGAGTACGAAAA | 57799 |
| rs537660136 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:615915 | TGTAGTGACCCGAGA[A/T]TGTGGCACTGCACTG | 57799 |
| rs537783823 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:610754 | CGCCCTGCCCCACCC[C/T]GTCACCTGCTTGCCC | 57799 |
| rs537817166 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589883 | GAAGGAGGGCGGCGG[A/G]CGACCTCTGGTGACT | 57799 |
| rs537875524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:605472 | CCTCGCCCTCTGCAG[A/G]CCTCTCACACTCTGC | 57799 |
| rs537886389 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629410 | ACCGGGCTGACCTGC[C/T]GCGGTTGGCTGGGTT | 57799 |
| rs537892931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:624134 | TGGCTTGTCGTTGTT[A/G]TCAGCGCCACTGTGA | 57799 |
| rs537907427 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:622271 | ATATTGCCACCGTTA[C/T]CCAAGAGCTGGCGCA | 57799 |
| rs537995101 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:600714 | CCGAGTTTGCACCAC[C/T]ACACTCCAGCCTGGG | 57799 |
| rs538040434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:621552 | CGCGAGGCCCTTCAC[A/G]TGCCGCCGAAGGCCG | 57799 |
| rs538194756 | in-del | -/AGTT | 0.0023933 | 0.0345097 | intron-variant | RAB40C | GRCh38.p7 | 16:608125 | GTTTAATTGACTCAC[-/AGTT]AGTTCCGCATGGCTG | 57799 |
| rs538198680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:605788 | CAACACAGGTGCCCA[C/T]TGCTGTTGGGACGTA | 57799 |
| rs538212176 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:590856 | TGGGCTCGGGGGAAG[A/G]TGTCGTGGGCCGGAG | 57799 |
| rs538319843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596259 | GAGGTGGGCGGGAAG[A/G]ACACAAGGGAGGGAT | 57799 |
| rs538405808 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RAB40C | GRCh38.p7 | 16:591256 | GGATCATCTGGGGTC[C/T]GAGGGAAGGTGTCAT | 57799 |
| rs538424750 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:604963 | CTTGGGAGGCTGAGG[C/T]AGGACAATCACTTGA | 57799 |
| rs538543076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:591636 | CTCACTCTGTCGCCA[A/G]GCTGGAGTGCAGTGG | 57799 |
| rs538573798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:605849 | GTGTAGATGCTGCCA[A/G]CCCGTTCTCCAAAGC | 57799 |
| rs538585495 | snp | C/G | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593843 | AGGGAGTGCTTCATG[C/G]TCTCTTCAGGATGGA | 57799 |
| rs538609723 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:601387 | AGGCTGTTCTGCTCG[A/G]GAGCAACAGTGTCCA | 57799 |
| rs538615593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596336 | CAGCTGAGAAGGCGC[A/G]AAGCTGCTGGTCCCT | 57799 |
| rs538624343 | snp | A/G | | | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595823 | GGCCAGGCTGGTCTT[A/G]AACTGCTGACCTTGT | 57799 |
| rs538670677 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:601025 | CTGCCTCTGCATTTA[C/G]ACCCTTAGCCTCCTT | 57799 |
| rs538681220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:625310 | GCTCATCTGCCCATC[C/T]GCCAAGTAATAAGCA | 57799 |
| rs538698620 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:626278 | CAGGTCAGTGACTTG[C/G]TAAGAGCAGCCTCGG | 57799 |
| rs538701536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:621500 | CCACTCCCCGCTGCC[A/G]TCACCTGTCACACAG | 57799 |
| rs538884118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:626735 | CTGAGGTCAGGACTT[C/T]GAGACCAGCCTGGCC | 57799 |
| rs538888341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622203 | GTTCTACTTCTGGGA[A/G]TTTATCGTGTAGGTC | 57799 |
| rs538951640 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RAB40C | GRCh38.p7 | 16:605396 | AAAAAACCCCTTTAA[A/G]GTCTGCAATACAGTG | 57799 |
| rs539030049 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:605549 | TCACGTCAATGGAGC[C/T]ACACAGGGCAAACTC | 57799 |
| rs539102828 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628431 | TACTTGATGGGCAGC[A/G]GTGCAGACCCCGGGC | 57799 |
| rs539107905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:591706 | AAGCGATTCCCCTGT[C/T]TCAGCCTCCCGAGTA | 57799 |
| rs539164681 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627865 | GGTCGGAAACAAGCC[A/G]GGCCTCCCCAGCTGC | 57799 |
| rs539317977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:619946 | TCCTGGGAGTTCCCT[C/T]GGAGATGTTGGCAGC | 57799 |
| rs539373797 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:620374 | CGCCAACCTGGGCGA[C/T]GAGTGAAACTCCATC | 57799 |
| rs539516679 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594180 | AGCAAGTTTTCCTCC[C/T]GCCACGTTGGTCAGG | 57799 |
| rs539581620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593717 | CACACGCCCAGCACC[C/T]GTGGGAGCCCCTGTG | 57799 |
| rs539595079 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:610755 | GCCCTGCCCCACCCC[A/G]TCACCTGCTTGCCCT | 57799 |
| rs539596986 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:619486 | TCTGCTGGCGAATGT[C/G]AGGCCGGAAGGAGGG | 57799 |
| rs539606317 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594477 | GAGGGCACCCTGTGT[C/G]GGTGTCCCAGCTTCT | 57799 |
| rs539610091 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589069 | AGAGCGCGGTCCGGG[C/G]CCTGGGTCCCCGTCC | 57799 |
| rs539681920 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:614797 | GCCAAACTCTACCTC[A/G]TCCCGACGGTGAACT | 57799 |
| rs539746497 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589607 | CGACCCAATGGCGCC[A/G]GCGACGGGGCGGGCG | 57799 |
| rs539825604 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:619038 | GGTGTGGTGTACTTG[C/G]AGCTGTGTGTGTGCA | 57799 |
| rs539830698 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:609333 | GCAGACACCACTGGG[C/G]ATGGTGGGGGACAGG | 57799 |
| rs539841970 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:625894 | GCTGAGTTCTGTGCC[C/T]CCAGCATGCACCCGG | 57799 |
| rs539869468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593771 | GGGTGTGCGCTGGGT[C/T]TCTGGATCTCTAGGT | 57799 |
| rs539882365 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:608573 | CCCTTTACCATCCTG[A/G]AAAGAATGAAACTCG | 57799 |
| rs539890209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:623371 | AAAATCATGCTGGGC[C/T]GGGCGCGGTGGCTCA | 57799 |
| rs539965516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:604464 | TGTGAGTCCTTCTGA[A/G]GGTGTTTCTCTAGAA | 57799 |
| rs540016127 | snp | A/T | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588018 | ATCACGATGTTGGCC[A/T]AGCTGGTCCTGACCT | 57799 |
| rs540048202 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:608727 | ATGCAAAAAAAATTA[C/G]CTGGGCATGGTGGCG | 57799 |
| rs540050983 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:605013 | GAGTGAGCTGAGATC[A/T]TGCCACTGCACTCCA | 57799 |
| rs540112546 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595554 | TGGCATCTGAGAACC[C/T]ATGTGGTCAGGAGGT | 57799 |
| rs540295516 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:614406 | CCTAAACCTCGTCCC[A/G]ATGGTGAACTGCCTA | 57799 |
| rs540331233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:624268 | CCCACTCCCCAGTCT[C/T]TCCACCTCCCCCAGC | 57799 |
| rs540391059 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629116 | GCCAGCAGGGCCCTT[A/G]TTTGGGATTATGAAC | 57799 |
| rs540404511 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594714 | GGTGACTGGACAGCC[A/G]TGCGTGGCTTCCCTG | 57799 |
| rs540461388 | snp | C/G | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595468 | ACACCTGCTTCTGCT[C/G]CACCGCGCACACTAA | 57799 |
| rs540485147 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:601162 | AGCTGTAGCTCCCAC[A/G]TGTGTGTGGAGCTGG | 57799 |
| rs540492109 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:590094 | CCTGGTGGTGCGGGA[A/G]GCGGCGGGGCGGCGG | 57799 |
| rs540553185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:609467 | CGTCAGCCCAAAAGA[A/G]GCGGCCACGAGACGC | 57799 |
| rs540564578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:604284 | TACAGAAAACACGTC[A/G]TTTTAGCCATATGTA | 57799 |
| rs540588040 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588177 | ACCCCCCGCTTCCAG[C/G]CAGTCTCAGAAACCG | 57799 |
| rs540649319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:599207 | CCCAGGCCCCGGCCC[C/T]GGCCGAAGCTGCCAC | 57799 |
| rs540649382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:604514 | GGGTGTTTCTCTAGA[A/G]TACACGTGAGTCTTT | 57799 |
| rs540755569 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:621307 | GTGCATCCAGCCGAG[A/G]TGCAGAGCCCAGGTT | 57799 |
| rs540811969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:620797 | GGCATCCCAGCCCCC[C/T]GCCGACGGGCTCCAC | 57799 |
| rs540825699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:592537 | GCCCCTGCACCTGCC[A/G]CCTCCTGGTCCTGCA | 57799 |
| rs540841435 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595243 | CGGTGGGCGCTTTCC[C/G]CTGCCCCCGTGTAGC | 57799 |
| rs540873457 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:620218 | ACCAACATGGTGAAA[A/C]CCCATCTCTACGAAA | 57799 |
| rs540885088 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:611266 | GGCCCTGGGCCATGG[C/T]GCCATCTAGGGGTGG | 57799 |
| rs540888986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597371 | GTCCTCAAACCAAAC[C/T]GGGAAGGATTCGAAT | 57799 |
| rs540915509 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:626929 | GCGACAGAGCGAGAC[C/G]CGTCTCAAAAAACAA | 57799 |
| rs540971178 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587452 | CCGTCCCTCCCTTCA[C/G]TGGGCCTGCTGCCCT | 57799 |
| rs541007909 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | RAB40C | GRCh38.p7 | 16:607516 | CAAAAAAAAAAAAAA[A/C]CGGGGGGCCGGGCGC | 57799 |
| rs541035019 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:601211 | GTAGTACCAAAAACT[A/C]TGATTTTTTGTGTGT | 57799 |
| rs541046469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:614004 | AAGGCTGCGGCCTCT[A/G]CTGCATCCAGATGGT | 57799 |
| rs541131459 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:603538 | AGGCTGTCTTGTAGG[A/G]TAATCCGGTCCCCTA | 57799 |
| rs541134341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:607754 | CGAGATCGCGCCACT[A/G]CACTCCAGCCTGGGC | 57799 |
| rs541142526 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:598049 | CAAGAGATTGAGACC[A/T]TCCTGGCCAACATGA | 57799 |
| rs541154246 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596903 | GGGGATGGCGGCGCA[C/G]TCTGATACAGGCAGT | 57799 |
| rs541210988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622569 | CTGGAGTGCCGTGGC[A/G]CGATCTCGGCTCACT | 57799 |
| rs541221444 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:603424 | GGAGTGGTATGCCGG[A/C]AGATTGAATGCGGAG | 57799 |
| rs541273969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622383 | CTTGACCCCGCCCGC[A/G]AGGCATGAGCGGCAC | 57799 |
| rs541477099 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:602120 | AACAGCTCTCAAAAC[A/G]AAACAAAAAACTACT | 57799 |
| rs541479543 | snp | C/T | 1.7127e-05 | 0.00292629 | intron-variant | RAB40C | GRCh38.p7 | 16:618185 | CCCGGCCCCTCCCCT[C/T]CCCGTATGTTTCAGG | 57799 |
| rs541483936 | in-del | -/AA | 0.0111196 | 0.0737302 | intron-variant | RAB40C | GRCh38.p7 | 16:613137 | CTGGCCTGTAGAATC[-/AA]GAGCAGGGACAGCCG | 57799 |
| rs541626471 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587884 | ACAATCTCAGCTCAC[C/T]GCAACCTCCGTTTCC | 57799 |
| rs541662941 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | RAB40C | GRCh38.p7 | 16:616584 | ACCTCATGATCCGCC[C/T]GCCTCGGCCTCCCAA | 57799 |
| rs541707406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622846 | TCAGTTTTAGAAAAC[A/G]GAAGGCAGTGGAAGA | 57799 |
| rs541799140 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597442 | TGATGAAAGACATGC[A/C]CATCCTGTGAGAGGG | 57799 |
| rs541929281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:626985 | GGGAATGAGTCAGGA[C/T]GCGCGCTCCCCCGCT | 57799 |
| rs541969853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593943 | CAGGAGTGTGGGTGG[C/T]GCACGCGGCGGGGAG | 57799 |
| rs541985568 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:603518 | TCTGGCTCTGATATG[A/T]GTTCAGGCTGTCTTG | 57799 |
| rs542032947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:598681 | TGGGAGGTGGTGGCT[A/G]CAGTGAGTCTGACTG | 57799 |
| rs542111740 | in-del | -/GAGCCGAGATTGTGCCATTGCACGCCAACCTGGGC | 0.0376037 | 0.131863 | intron-variant | RAB40C | GRCh38.p7 | 16:620337 | GGTGGAGGTTGCAGT[lengthTooLong]GACGAGTGAAACTCC | 57799 |
| rs542117733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:614038 | CTGCCTAACTCTACC[A/G]CGTCCCGATGGTGAA | 57799 |
| rs542139235 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589187 | GCGTCCCCGGGCGGA[A/G]GGCTCACGCTCGGTG | 57799 |
| rs542159070 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594310 | GCTGAGTGACACTCC[A/G]GTCCTTTGAGCCTGG | 57799 |
| rs542177045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622755 | GTGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 57799 |
| rs542196806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:602732 | GCCACTGTGCCTGGC[C/T]AATAAATTATTTTTT | 57799 |
| rs542217525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:607785 | GACAGAGCAAGACTC[C/T]GTCTCAAAAACGAAA | 57799 |
| rs542236453 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594136 | GGCAGTTCCACCCTC[A/G]GCACCGTGTCCCCAC | 57799 |
| rs542253775 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:605266 | GCCCCATTGTTTCAT[A/C]GTCCCATCAGCAATG | 57799 |
| rs542264397 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:624139 | TGTCGTTGTTATCAG[C/T]GCCACTGTGACACAC | 57799 |
| rs542266235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:610130 | TAGCTGGTGGGGAAG[C/T]GGCACCCTGTGCGGT | 57799 |
| rs542369372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595983 | CAGTAGGTAGAATAT[C/T]GAATGTTAAGTTTGT | 57799 |
| rs542430765 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:600595 | GTCTCTACTAAAAAT[A/T]CAAAAATTAGCTTGG | 57799 |
| rs542471109 | snp | A/C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628051 | CACTTGGGACTCCTC[A/C/G]AGAGGGGACTCGCGG | 57799 |
| rs542547600 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588729 | TGCTCCTCGCCGGCG[A/G]GGCAGACGTGACGGG | 57799 |
| rs542577229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:625645 | ACTGTCCCACGGCCT[A/G]CGCCTGGGCATGCTG | 57799 |
| rs542597517 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:591079 | GGAAGGCATCATGGT[A/C]CTAAGGGAAGCTGTC | 57799 |
| rs542598543 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:616974 | CACTGTATGGACCAC[A/G]CTCCTGCCCTGCCCT | 57799 |
| rs542613383 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:611927 | CCGCCCTGGCCTGTA[C/G]AATCAAGAGCAGGGA | 57799 |
| rs542661962 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:621736 | AACTGCAGTGTGGCT[A/G]ACGGGATGTGCCATC | 57799 |
| rs542676076 | snp | C/T | 0.000489117 | 0.0156307 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629621 | TCCAGTCAGTCGGCC[C/T]GCTCAGCAGAGCCGC | 57799 |
| rs542725304 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:624520 | AACAGGACCTGGGGC[C/T]ACACTTCAGTCTTCC | 57799 |
| rs542728324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:611554 | TGACGGCCTGAGCGC[A/G]GTGCCTCCCTGAAGA | 57799 |
| rs542735342 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:614999 | GGGCTGCTCACAGCC[C/G]TGGCCCTTTTGGCAC | 57799 |
| rs542740270 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RAB40C | GRCh38.p7 | 16:605615 | GGTGAGCTTCGGCCA[C/T]GTGGTTGAGTGCAGT | 57799 |
| rs542773848 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:616407 | GCAGTGACATGATCT[C/T]GGCTCACTGCAACCT | 57799 |
| rs542819175 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:619645 | CTCCGGGGCCAGTTC[A/G]TGAGCCTGGAGCCCC | 57799 |
| rs542828189 | snp | A/G | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594336 | CCTGGCAAGTTGTGG[A/G]GAGAAACGGAGGGAG | 57799 |
| rs542985926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:607262 | AGCGCTTTGGGAGGC[C/T]GAGGTGGGTGGATAA | 57799 |
| rs543085064 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:605664 | GCCGAGTGGTCTCCC[A/G]TGTGTCAAGGCTGCA | 57799 |
| rs543102381 | snp | A/G | | | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596101 | AGGGCAAATGCTTGC[A/G]TGGCAGGTGCACGGC | 57799 |
| rs543166178 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:591484 | TATAGGCACGCTGTT[C/G]CCCTGAGGTATTTGC | 57799 |
| rs543202754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596726 | GAGCAGCTGTGGGAA[A/G]AAGGACTGGCTGCCA | 57799 |
| rs543203047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:606886 | CCCACCTCGAGATCC[A/G]TGCACCTTAATCCTG | 57799 |
| rs543226310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596440 | GAGTCCTCCCCTGCG[C/T]AGCACATGGTACGAT | 57799 |
| rs543338369 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:599352 | GCCCTAGTGGCTGCC[C/T]GCAGAGTCTTGCGCC | 57799 |
| rs543352396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:591808 | CAGCATGTCGGCCAG[A/G]ATGGTCTCAATCTCC | 57799 |
| rs543371201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:601718 | CGGTGGTGCACGCCT[A/G]TAATCCCAGCTACTT | 57799 |
| rs543389405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:613206 | TCACCTGTAGAATCA[A/G]CAGGGACAGCCGCCC | 57799 |
| rs543429710 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:617640 | CTGAGGTCAGGAGTC[C/T]AAGACAAGCCTGGCC | 57799 |
| rs543474830 | snp | C/T | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:613531 | GCCAGTTGCCCTTTT[C/T]TGCGAGGCTGGATCG | 57799 |
| rs543540783 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RAB40C | GRCh38.p7 | 16:611291 | GGGTGGCCTAGGGGA[A/G]TCCCCGGGCCATCAG | 57799 |
| rs543652868 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622337 | GAGCTCAGGGCGTGC[C/G]GGTGGGAGCAGCGCC | 57799 |
| rs543696761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:627007 | TCCCCCGCTCTAGGG[A/G]ATGAGTCAGGACGCT | 57799 |
| rs543756738 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:626361 | GGGTGCCGCCGTGGC[C/T]GCTGCACTCTGCCAT | 57799 |
| rs543791759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:615042 | TTCTTGTCTTGGAAA[C/T]GAGGACCCGAGGGAG | 57799 |
| rs543876130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:615461 | AAGCCCCTTGGAGAA[A/G]GTGTCATAAAAAGAC | 57799 |
| rs543878022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:608959 | TGACTGTACAAAAGA[C/T]ACAAAATTAGCCAGG | 57799 |
| rs544075476 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:604646 | CTTTCTGAAGGTGTT[G/T]CTGTTCCCTTAGGTA | 57799 |
| rs544093931 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629213 | GTTAGACACTCCGCC[A/G]TTCCTGGTTCTCTCC | 57799 |
| rs544207077 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:599560 | TGTTCGCTACTGTCA[A/G]CGTGGATTCAGCAAG | 57799 |
| rs544211406 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:612476 | CGCCCTGGCCTGTAG[A/C]ATCAAGAGCACGGGA | 57799 |
| rs544227392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629617 | GTCCTCCAGTCAGTC[A/G]GCCCGCTCAGCAGAG | 57799 |
| rs544283222 | snp | A/C/G/T | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:621527 | ACAGCAGCAGTCCCG[A/C/G/T]GGCTCTTCCCGCGAG | 57799 |
| rs544332847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:620833 | GCATCCCAGCCACCC[C/T]CCCCGACGGGCTCCA | 57799 |
| rs544396053 | snp | A/G | 0.00610484 | 0.0549104 | intron-variant | RAB40C | GRCh38.p7 | 16:625056 | GTCCCAGGTACTCCC[A/G]GGGGGATTCACTGAT | 57799 |
| rs544570972 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595288 | GTGAGAAGGCAGCAC[C/G]ACCCCCACTGTGCAG | 57799 |
| rs544583724 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:609723 | TAAGCAGCACATTTT[A/T]AAAAAGCCATAGAAG | 57799 |
| rs544630356 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594842 | TTTTTTTTTTTTAGA[C/G]GAAGTCTTACTCTCT | 57799 |
| rs544648060 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:625582 | GCCCCGGGTAGGCTC[G/T]GGATTCCCGCCTGCC | 57799 |
| rs544721437 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:615606 | TGTCCAGAACTGTCT[G/T]CTCCTTTCAGTTTCT | 57799 |
| rs544755279 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:590535 | CAAGCGCCGCCGAAC[G/T]TTCCCAGGAACGCCT | 57799 |
| rs544828996 | snp | C/G | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589176 | CTGTGGCGGCCGCGT[C/G]CCCGGGCGGAAGGCT | 57799 |
| rs544829892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:621340 | CAGCAGGGTTTCTCC[C/T]GCCGCCCCTGATGAG | 57799 |
| rs544853824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:591875 | GCTGGGATTACAGAC[A/G]TGAGCCACTGCGCCT | 57799 |
| rs544859048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:616113 | ATACAAAAAATTATC[C/T]GGGCATGGTGGCGGG | 57799 |
| rs544863812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:625080 | CACTGATGGACTGGC[C/T]GAGAGGACACTTAGC | 57799 |
| rs544871841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:600070 | GCGTGGATTTGCAAA[A/G]TTTTGTTCCCTTGTG | 57799 |
| rs544997444 | snp | C/T | 0.00196431 | 0.0312778 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629660 | TGGCCAATCTGGTGT[C/T]TGCTATGCCCGGCCC | 57799 |
| rs545007730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595366 | GGTCCGGGAGGAGCC[A/G]CCCTGCAGGCCTCCT | 57799 |
| rs545032064 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:620624 | GGCATCCCAGCCCCC[C/G]CCGACGGGCTCCACC | 57799 |
| rs545127006 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:616568 | TGCTCTCAAACTCCC[G/T]ACCTCATGATCCGCC | 57799 |
| rs545320425 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:600576 | ACCAACATGGTGAAA[C/G]CCCGTCTCTACTAAA | 57799 |
| rs545326334 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593134 | GCTTTCTGTGTCTAA[A/G]GTCTCAAGGTTAAGA | 57799 |
| rs545344090 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | RAB40C | GRCh38.p7 | 16:612976 | ATCAAGAGCAGGGAC[A/T]GCCGCCCTGGCCTGT | 57799 |
| rs545407310 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595935 | AAGTTGGACTGGCAT[C/G]GCCTTACTTAAATTT | 57799 |
| rs545414122 | snp | C/G | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594561 | ATCTGGCTTGAAGTT[C/G]GTGGCTCCGAAGTGG | 57799 |
| rs545420040 | snp | A/G/T | 3.5024e-05 | 0.00418461 | synonymous-codon | RAB40C | GRCh38.p7 | 16:627598 | CCCCCAGAACTGCTC[A/G/T]CGGAGTAACTGCAAG | 57799 |
| rs545448567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:623225 | TTTTCAGTGTCATGC[A/G]AATAGGGGTGTTTGC | 57799 |
| rs545506003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:598043 | CGAGGTCAAGAGATT[A/G]AGACCATCCTGGCCA | 57799 |
| rs545564943 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:611471 | CAGGACCAAAATGAC[C/T]AAGGCCCCTCCGTCC | 57799 |
| rs545568655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:591378 | AAGGTGTCATGGGCC[C/T]GGGGAAGGTGTCACG | 57799 |
| rs545624370 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:616909 | CCATTCCAGGCAAGC[C/T]GTGCCCATGGAGAGG | 57799 |
| rs545655604 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | RAB40C | GRCh38.p7 | 16:614375 | CCAAACTTTACCTCG[G/T]CCCGATGGTGAACTG | 57799 |
| rs545685013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:606313 | ACACACAGTCCTCTC[A/G]GTCCTCAGTCCAGTG | 57799 |
| rs545892935 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588366 | CAAGGCGCCATCTCT[A/G]CAAAAAATACAAAAG | 57799 |
| rs545950895 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589251 | CAGACTCACTGGTGA[C/T]CCAACGGTGCGCCCC | 57799 |
| rs546017072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:599147 | CGAGGTGCTGTGTTT[C/T]GGTCCAGAAAGTCAC | 57799 |
| rs546020490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:614044 | AACTCTACCGCGTCC[C/T]GATGGTGAACTGCTA | 57799 |
| rs546103413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594368 | CGGTTGTGGACATGG[C/T]GAGGCTAACATCACG | 57799 |
| rs546177594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:598832 | TTGTACAGCGGCCGG[A/G]TGTAAGAACCTCATG | 57799 |
| rs546208914 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RAB40C | GRCh38.p7 | 16:604249 | TTAAATTTTTTTTTT[A/T]AATTATTTTTCTTGT | 57799 |
| rs546221368 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:603678 | GTACAGTTCTATGAG[C/T]TTTGGCACATATATG | 57799 |
| rs546222948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:608641 | TTAGGAGGCCGAGGC[A/G]GGCAGATCACTTGAG | 57799 |
| rs546233020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:618508 | GATTCTCCTGCCTCA[A/G]CCTCCCCAGTAGCTG | 57799 |
| rs546262549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:614098 | ACTGCCGAACTCTAC[C/T]GCATCCCGATGGTGA | 57799 |
| rs546309231 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628592 | CTCGTCCACGTCCAC[A/G]TCCACCTGGGGGCCT | 57799 |
| rs546340686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594635 | ATTGTCCTGATGTGT[C/T]GTCGGCTGCTTATCC | 57799 |
| rs546348575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:607914 | TCAGACCCCTTCCTC[C/T]CCCTCCACTGCCCGT | 57799 |
| rs546445823 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628979 | CTGGGAGATGAGGGC[C/T]GTGGCCTGCATGAAC | 57799 |
| rs546533700 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:624190 | TGTGGGCTTGCCATG[A/C]GGGAGGTTGCCATGC | 57799 |
| rs546620688 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:613784 | AACACCCAGGTCTAG[A/C]CCCAGGTGGAATGCA | 57799 |
| rs546638329 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588021 | ACGATGTTGGCCAAG[C/T]TGGTCCTGACCTCAG | 57799 |
| rs546678232 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595473 | TGCTTCTGCTGCACC[A/G]CGCACACTAAGTTCT | 57799 |
| rs546693831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594087 | AAGCCCAGCCGCTCC[C/T]GCTCTGCAGGGGGCA | 57799 |
| rs546696481 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:627309 | GCCTCCTCCCCCACA[A/G]CCCCATGGTCTGACA | 57799 |
| rs546715458 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597730 | CTGACTTCAAGCAAT[-/C]CGCCCGCCTCAGCTT | 57799 |
| rs546807458 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:598302 | AGAATGGCGTGAATC[C/T]AGGAGGCAGAGCTTG | 57799 |
| rs546863675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:609176 | TGGTTTGGGAACAGC[A/G]GTGCTGCCACGGCTG | 57799 |
| rs546928406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594397 | CGGTTTGCTGTGGAT[A/G]TTGGGGCCTGGTGGT | 57799 |
| rs546946238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:598911 | CAGCAGCTCCAGCAG[C/T]GTGGGTAACCCGGTG | 57799 |
| rs547074073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596492 | CTGGGGCCCAGGGGC[C/T]ACGTCAGCCAGGGTG | 57799 |
| rs547085675 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:626804 | TTAACCGGGCGTGGT[A/G]ACGCACACCTGTAGT | 57799 |
| rs547090749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:623995 | TACCTCACCTGGGTT[A/G]CACATCTCTCCTTGG | 57799 |
| rs547113392 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589421 | GGCACAGCCTGCGAG[A/G]GGCTTTCGTTTCCCG | 57799 |
| rs547124454 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:607215 | GTTGAAAACAAAGTC[G/T]CCTGGGCACGGTGGC | 57799 |
| rs547135067 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:616729 | CTTGGAAATACATTC[A/G]CCTTGGAGAATTCAA | 57799 |
| rs547140224 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:619381 | CACTGGGGCCATGTG[G/T]GCAGTGTGTGTGCAG | 57799 |
| rs547196236 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628450 | CAGACCCCGGGCACC[C/T]GCGTGCAGCCTCCTG | 57799 |
| rs547243538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:609770 | TGAGGACATCTCCCA[A/G]AAAATAGAACAAAAA | 57799 |
| rs547258481 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:617431 | TTTTACTCCAACAGG[A/C]AAAAGACAGTCTGGG | 57799 |
| rs547259327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:606625 | GGGAGGTTGGCAGAA[C/T]TCCGTTCTTGCTGGT | 57799 |
| rs547380911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:601909 | GAGGTGGGTGGATCA[C/T]GAGGTCAGGAGATTG | 57799 |
| rs547393254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:601405 | GCAACAGTGTCCACA[C/T]GTCAGTTTCCAGAGC | 57799 |
| rs547393467 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:607068 | GAGCCGAGGGTGCTA[C/T]GCAGGCTCAGCAGCC | 57799 |
| rs547454409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:602366 | TTCTAGTGATCCTCC[C/T]GCCTCAGCCTCTCAA | 57799 |
| rs547538810 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:626197 | GGAGGCTGAGGGGGG[C/G]CAGGGGCCAGTGAGG | 57799 |
| rs547550993 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RAB40C | GRCh38.p7 | 16:611702 | AATCAAGAGCAGGGA[C/T]AGCCGCCCTGGCCTG | 57799 |
| rs547615790 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:617124 | CGTGGGTCTTGGCCC[C/T]GGGAGGCCAGTGGCC | 57799 |
| rs547643041 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:618013 | TTCTGCTGCCTGCCT[A/G]GCTCAGCGGCACGGC | 57799 |
| rs547670230 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:592829 | CCACACAGCCAGGAG[C/G]TGGAGAGACAGGACC | 57799 |
| rs547680671 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597777 | TTACAGGCATGAGCC[A/T]CTGTGCCCAGCCCAG | 57799 |
| rs547704001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622717 | CACCATGTTGGCCAG[A/G]ATGGTCTCCATCTCT | 57799 |
| rs547712571 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:627166 | GGATGGGGTGCCAGT[A/G]GACACATCTGTGCTG | 57799 |
| rs547778186 | in-del | -/ACTC | 0.0023933 | 0.0345097 | intron-variant | RAB40C | GRCh38.p7 | 16:608259 | TCAGGTGTCGGGAGA[-/ACTC]ACTCACCCGCACAAA | 57799 |
| rs547864003 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:626795 | ATACAAAAATTAACC[A/G]GGCGTGGTGACGCAC | 57799 |
| rs547900574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597060 | GGGCGGAAGACCAGG[A/G]CACGACCAGACACCG | 57799 |
| rs548002556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622408 | CGGCACCGTGGACAC[A/G]TCTGTAGACGCTGAG | 57799 |
| rs548020468 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:610680 | GCCGTCCCCCAGCGC[A/G]GGCTCCAGGCCTCTC | 57799 |
| rs548102552 | snp | G/T | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588557 | GGTGCGTCGATGTGG[G/T]CGCCGCTTAGTCAGG | 57799 |
| rs548139690 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:599132 | ACTGATCAGGGTTGC[C/T]GAGGTGCTGTGTTTC | 57799 |
| rs548142916 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587708 | CAGTGGCCCACGGCT[G/T]GGTCTGGAGAGCGTT | 57799 |
| rs548165927 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597875 | GGAGGCCGAGGTAGG[C/T]GGAGTGCTGGAGCCC | 57799 |
| rs548178916 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:598654 | GGCTGAGGTGGGAAA[C/G]TCACTGGAGCCTGGG | 57799 |
| rs548181956 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | RAB40C | GRCh38.p7 | 16:591587 | GTTTTGTTTTCTTTT[C/G]TTTTCTTTCTTTTTT | 57799 |
| rs548268216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:617466 | TGTGTCCCTAGAGAT[C/T]GCGGCTCCCCTCCTG | 57799 |
| rs548292934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:602405 | GACCATAGGCATGCA[C/T]CACAACACCTGGCTA | 57799 |
| rs548320348 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:617153 | CCGAGGCTGGTCTCG[C/T]GGGCGCTCGCTCCAG | 57799 |
| rs548353890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:607093 | GCAGCCAGCCTCCCT[C/T]GGCTGCCTTACAGCA | 57799 |
| rs548391533 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:613623 | TGCTTCTTGGTCGTC[A/G]GTTTTTCTTCTTTGG | 57799 |
| rs548454562 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:613325 | AGGGACAGCCGCCCT[A/C]GCCTGTAGAATCAAG | 57799 |
| rs548487297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:618672 | CGCAGGTGTGGTGTA[C/T]TTGGAGCTGTGTGTG | 57799 |
| rs548529147 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:623013 | ACTGTGACCCACGCC[A/G]GAGCAAGCCTCCGGG | 57799 |
| rs548560519 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:599606 | GGCATCAGTCAGCGT[A/G]GATTCAGCAAGGTTT | 57799 |
| rs548611740 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:601846 | AAAAAAAAAAAAAAA[A/G]GCCGGATGCGGTGGC | 57799 |
| rs548622035 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:601853 | AAAAAAAAGGCCGGA[G/T]GCGGTGGCTCACGCC | 57799 |
| rs548652151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622747 | TTGACCTCGTGATCC[A/G]CCTGCCTCGGCCTCC | 57799 |
| rs548670317 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:610253 | GCCTGTCCTGTGGAG[C/T]GGCTCTGACCAGGAC | 57799 |
| rs548671006 | in-del | -/TTATTTATTTATTTATTTATTTAT | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:616341 | GCAGCATTTTATTTA[-/TTATTTATTTATTTATTTATTTAT]TTTATTTATTTATTT | 57799 |
| rs548693167 | snp | C/G | 1.9735e-05 | 0.00314119 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627661 | GCAGATGCCAGGAGG[C/G]CTCGAGCTGGACACT | 57799 |
| rs548698005 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595060 | CTGACCTCAAGTGAT[C/T]CACCTGCCTCGGGGG | 57799 |
| rs548698127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:600146 | TTGATGTTGGAGCCT[C/T]TTCAGGTGGCACCTG | 57799 |
| rs548708526 | snp | A/G | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587439 | GCTGCCCCAGAGTCC[A/G]TCCCTCCCTTCACTG | 57799 |
| rs548782745 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595382 | CCCTGCAGGCCTCCT[C/G]TGAAGCAGCGGGCTT | 57799 |
| rs548816160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:619201 | TGGGTGCACTCAGGG[C/T]CATGTGTGTGTGCAG | 57799 |
| rs548825114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:616237 | CTCCAGCCTGGGTGA[C/T]TGAGCAAGACTCTGT | 57799 |
| rs548827024 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:621446 | CTGGAAGGTCCCCGC[A/G]GCCTGGGTCTTGCAG | 57799 |
| rs548888444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:620978 | TGCATTTGCCAGGCT[A/G]AGGTCCTGGAAAGCA | 57799 |
| rs548898545 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:620230 | AAACCCCATCTCTAC[A/G]AAAAATACAAAAATT | 57799 |
| rs548973180 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:604876 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCGTATC | 57799 |
| rs549015701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:616591 | GATCCGCCCGCCTCG[A/G]CCTCCCAAAGTGCTG | 57799 |
| rs549057621 | snp | C/G/T | 0.000136082 | 0.00824758 | utr-variant-5-prime | RAB40C | GRCh38.p7 | 16:590262 | CGGTGCTTCGGCAGG[C/G/T]GGCCGGCGCGGGGCG | 57799 |
| rs549059675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629698 | TGTGGACGCCCCGGA[A/G]GTCACAGCTGAGCTG | 57799 |
| rs549117053 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:590656 | GAGGGACGCGCCCAG[A/C]GGGGACGGTGCCATG | 57799 |
| rs549157597 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:610516 | TTTCACTGAGCCGGG[G/T]ATTAGCTTAGCTTAT | 57799 |
| rs549320905 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:606478 | GGTTTCCCTGAGCTG[A/G]AGTCAAGGTGTTGGC | 57799 |
| rs549429800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:605766 | AGGAGTCTCAGACGC[A/G]TTTGGTCAACACAGG | 57799 |
| rs549501572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:590751 | GATCTGGAGCCCAGG[A/G]GAAGGTGTCATGGGT | 57799 |
| rs549501669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596102 | GGGCAAATGCTTGCA[C/T]GGCAGGTGCACGGCA | 57799 |
| rs549600815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:600854 | CAGGTTTTGCCTGTG[A/G]GGAAACAGAAAGGTT | 57799 |
| rs549604453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:621053 | ACTGGTTATGTCTTT[A/G]TTTTGTCTTGTTAAC | 57799 |
| rs549616396 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:611194 | GTGGGTGGGTGACGT[G/T]GTCCCCAGGCTTTTC | 57799 |
| rs549742853 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:606548 | TCCCTGGGCTGAAGT[A/C]AAGGTGTTGGCCAGG | 57799 |
| rs549760032 | snp | C/G | 0.000326264 | 0.0127682 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629753 | GGGACCAGACCACAG[C/G]CTCTGGCTCAGGTGC | 57799 |
| rs549760514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:617011 | CCCTGCCCGTGGCCC[A/G]TGTGCAGAAGTGGGC | 57799 |
| rs549760890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:600253 | TGCCTGCCCTGGAAA[C/T]GGCCATCTCTCTGAA | 57799 |
| rs549802783 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:611596 | CTTGTGAGTGTGCAC[A/G]GGACAGCCGCCCTGG | 57799 |
| rs549902550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:625236 | CCCCCTGCTGCAGTC[C/G]TGCCAGGTGAGGGCA | 57799 |
| rs549927250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:626260 | TAGGGGCTCGGCCGG[C/T]GGCAGGTCAGTGACT | 57799 |
| rs550063833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:626686 | CTCACTCCTGTAATC[C/T]CAGCACTTTGGGAGG | 57799 |
| rs550066541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:616671 | CTTGTTTGGCCCTCC[C/T]TAACACCAACCTTGG | 57799 |
| rs550096610 | in-del | -/CTG | 0.0142736 | 0.0832652 | intron-variant | RAB40C | GRCh38.p7 | 16:614205 | CATCCCTATGGTGAA[-/CTG]CTAACTCTGCCGCAT | 57799 |
| rs550104346 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596987 | ACGTTTGTCCTTCAG[A/C]AATTAGCGGAGGGAC | 57799 |
| rs550118415 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:601785 | TTCAGACTAGGCAAC[A/G]TAGCAAGGCCCTATC | 57799 |
| rs550200718 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RAB40C | GRCh38.p7 | 16:614523 | TGCCAAACTTTACCT[C/T]GTCCCGATGGTGAAC | 57799 |
| rs550221732 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:601318 | AGAGCAGGAGAAACC[A/G]TCTGTGTCCAGCCTG | 57799 |
| rs550329471 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628409 | GAGCTATCTGTAGAC[C/T]TAGGAATACTTGATG | 57799 |
| rs550403922 | snp | A/C/T | 3.82395e-05 | 0.00437244 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627638 | CGGGGATGGGCGGGG[A/C/T]CGCCTGTGCAGATGC | 57799 |
| rs550429687 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:620142 | GTTCACGCCTGTAAT[C/G]CCAGCACTTTGGGAG | 57799 |
| rs550466882 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628751 | TGCCCCAGCAGCCCC[C/T]CTGCACGGTCACCAT | 57799 |
| rs550531671 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:592101 | GCAGTCAGCATCCAG[C/T]CTCCCCAGAGTCCAT | 57799 |
| rs550589349 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RAB40C | GRCh38.p7 | 16:607954 | GATGCTGTGAGACCC[C/G]CTCTGAAGGGTGCCT | 57799 |
| rs550713690 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589530 | ACGTGGACTTCCGAG[C/T]CCCTGATTGGCGAGC | 57799 |
| rs550724061 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:619912 | GGAAGGACGCCAGGG[A/C]GGGCTGGGTCGCACC | 57799 |
| rs550763879 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:604319 | TACAGTTCAGTGGCA[C/T]TAGCACTAAACTATA | 57799 |
| rs550807264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:598927 | GTGGGTAACCCGGTG[A/G]GAGCCTGTGTGCTGC | 57799 |
| rs550871322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:604982 | ACAATCACTTGAACC[C/T]GGGAGGCGGAGGTTG | 57799 |
| rs550919469 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594454 | CTGCCTGCTGTACCC[A/T]TGGGAGCGAGGGCAC | 57799 |
| rs550946094 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | RAB40C | GRCh38.p7 | 16:590237 | TCTCTCACGCCGCGG[C/G]CTCACCCGGCGGTGC | 57799 |
| rs550983028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:624507 | CAACCTTGTTCTAAA[C/T]AGGACCTGGGGCTAC | 57799 |
| rs551004682 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:603996 | TTGATGCACATTTGG[A/G]TTATTTCCTGGTTTG | 57799 |
| rs551045751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:615699 | GGGCACGGTGGCTCA[C/T]ACCTGTAATCCCAGC | 57799 |
| rs551067048 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:620266 | AGCATGGTGGCGGGC[A/G]CTTATAATCCCAGCT | 57799 |
| rs551091809 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:607708 | AGGCAGGAGAATGGC[A/G]TGAACCCAGAAGGCG | 57799 |
| rs551161343 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:599272 | TTTGCTCCGAGGGGT[A/G]TCTGTGTCCTCAGGC | 57799 |
| rs551170707 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:610275 | GACCAGGACAGTGCC[A/G]TGTGTCTCATGGGGT | 57799 |
| rs551197352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:624059 | TCTTCAGCATCTGCA[C/T]GGTACATTTCACTGC | 57799 |
| rs551219296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:605370 | CTTTATTGAGGTGTA[A/G]TTTGTGTACAAAAAA | 57799 |
| rs551467966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:609867 | GCGGGAGCTGTGTGC[C/T]TGGAGGGGGGAGCTG | 57799 |
| rs551507778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596251 | GGAGCTGAGAGGTGG[A/G]CGGGAAGGACACAAG | 57799 |
| rs551550147 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594889 | CAGTGGCGCGATCTC[G/T]GCTCACTGCAACCTC | 57799 |
| rs551588218 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629258 | ACAGTAAATGTAATT[A/C]AGCTGTGGTCCCCAC | 57799 |
| rs551595510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589634 | GGCGAGGACAACGGC[A/G]TTGTGGGCCGGGGGC | 57799 |
| rs551730202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:611110 | GGGTGGGACGCAGAC[A/G]TCCAGCGGGAGGAGC | 57799 |
| rs551732793 | snp | A/C/G | 0.000312576 | 0.0124981 | utr-variant-5-prime | RAB40C | GRCh38.p7 | 16:590274 | AGGCGGCCGGCGCGG[A/C/G]GCGCAGGCGGCGCGG | 57799 |
| rs551984674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:605740 | TGGGTGACTCTCACA[A/G]GGCTCCTGTGAGGAG | 57799 |
| rs552005510 | snp | A/G | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:617876 | AGCATTTCCCAGAAC[A/G]TCAGCGTTGATGAGA | 57799 |
| rs552072732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:600784 | AGCTTTGGTGCCTAC[A/G]TGCGTCACACAGACA | 57799 |
| rs552159111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:602874 | CAAGCACAGCCAGAA[A/G]TGAGTCTTAAAGTGG | 57799 |
| rs552162667 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587613 | ACAGGCTGTGGTGGG[C/T]AGCTCCAGTGGGAGA | 57799 |
| rs552256490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:613673 | CTTTGCCCTTTTTTT[A/G]AAGTATAATTTCCGT | 57799 |
| rs552299827 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:598239 | AAAAATTAGCTGGGC[A/T]TGGTGGCGGGCACCT | 57799 |
| rs552317322 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:613372 | CCTCGTCTTTAGATT[C/G]AAGAGCAGGGACTGC | 57799 |
| rs552332330 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:602462 | TTTGAGACAAAGTCT[C/T]GCTCTTGTCCACCAG | 57799 |
| rs552376377 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588776 | GAGAGGGCTGCGCTG[C/G]GTCGGCGCTGACGTT | 57799 |
| rs552378923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:607859 | AAAAAGAAAAGAAAA[C/T]GAAGTCGCACCTAGT | 57799 |
| rs552379728 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RAB40C | GRCh38.p7 | 16:602618 | GTATTTTTTTAGTAG[A/G]GATGAGGTTTCACCA | 57799 |
| rs552401200 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:600480 | GGTGCCGGATGGGCA[C/T]GGTGGCTCACGCCTG | 57799 |
| rs552442531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:607606 | CAGGAGATGGAGACC[A/G]CGGTGAAACCCCGTC | 57799 |
| rs552500236 | snp | A/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:602183 | AAGTGTATATGCTTG[A/T]TATCTTAAGTATGTA | 57799 |
| rs552558289 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:604674 | GTAGATCTAAGAGTG[A/G]AATTGCTGTCATATA | 57799 |
| rs552611301 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RAB40C | GRCh38.p7 | 16:614555 | GCCTAAACCTCGTCC[C/T]GATGGTGAACTGCCT | 57799 |
| rs552666802 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RAB40C | GRCh38.p7 | 16:621939 | TGGATGTGAGTGGGC[A/G]CGGCTTGGCAGTAGC | 57799 |
| rs552705464 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628174 | GAAGCTTGGGTGACC[C/G]GGGCCCTGGCTCCCA | 57799 |
| rs552730205 | in-del | -/CTG | 0.00517822 | 0.0506191 | intron-variant | RAB40C | GRCh38.p7 | 16:614297 | CATCCCGATGGTGAA[-/CTG]CTAACTCTGCCACAT | 57799 |
| rs552741410 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RAB40C | GRCh38.p7 | 16:607224 | AAAGTCGCCTGGGCA[C/T]GGTGGCTCAACCCTG | 57799 |
| rs552864132 | snp | C/T | 6.59979e-05 | 0.00574409 | synonymous-codon | RAB40C | GRCh38.p7 | 16:627421 | CAAGCTTCCACTGCC[C/T]GTCACCATCAAGAGC | 57799 |
| rs552918119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:607658 | TAGGCAGGCGCGGTG[A/G]TGGGCGCCTGTAGTC | 57799 |
| rs552924716 | snp | A/C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:591778 | GTTGTGTGTATTTTA[A/C/G]TAGAGACGGGGTTTC | 57799 |
| rs552949505 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593154 | CAAGGTTAAGACGTG[C/T]ACAGCACAAGGAGCA | 57799 |
| rs552958259 | in-del | -/G | 0.00358779 | 0.0422022 | intron-variant | RAB40C | GRCh38.p7 | 16:622306 | AGTTCACGAGCAGGC[-/G]GGGGGTGCTGGGCCT | 57799 |
| rs553071056 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597383 | AACTGGGAAGGATTC[A/G]AATCCTGGATGGGTG | 57799 |
| rs553137159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:592575 | GTGACTGCCCCAGAA[C/T]TGGTAACTCCTGACT | 57799 |
| rs553137290 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:604167 | CAACTGATCCTCCCA[C/T]CTAGCAGCTCCCTAG | 57799 |
| rs553152372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:608131 | ATTGACTCACAGTTC[C/T]GCATGGCTGCAGAGG | 57799 |
| rs553190482 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:603435 | CCGGAAGATTGAATG[C/T]GGAGCGCCGGCCCCG | 57799 |
| rs553208292 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:598014 | CACTTTGGGAGGCCA[A/G]GGTGGGTGAATCACG | 57799 |
| rs553213598 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:614259 | TCTACCTCGTCCCGA[A/T]GGTGAACTGCCTAAC | 57799 |
| rs553217161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:599005 | CCTGGTCAGCAACGT[C/T]GTCGGCCACCTGGGC | 57799 |
| rs553241288 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627781 | GGTGCGAGGAGGAGC[A/C]TGCACGGACCAAGCG | 57799 |
| rs553369736 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628481 | TTCTCGGCAGCTTCT[G/T]TCGCTGGCCCTGGGG | 57799 |
| rs553394416 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | RAB40C | GRCh38.p7 | 16:614579 | ACTGCCTAACTCTAC[C/T]GCATCCCGATGGTGA | 57799 |
| rs553438629 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:618854 | GTGTATGTGCAGGCA[C/T]GTGCACAGGTCTGGC | 57799 |
| rs553496379 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:590887 | GGAAGGTGTCATGGG[C/T]GCAGGATCTGGGGTC | 57799 |
| rs553521896 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RAB40C | GRCh38.p7 | 16:605985 | AGCCATAGAACATTT[C/T]TATTCTGTCAGTAAC | 57799 |
| rs553530090 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RAB40C | GRCh38.p7 | 16:600579 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 57799 |
| rs553534106 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:605853 | AGATGCTGCCAACCC[A/G]TTCTCCAAAGCAGTC | 57799 |
| rs553578462 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:608390 | CAGCCAAATCTTATC[A/G]CTCCTGAGCCTGCTT | 57799 |
| rs553597271 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:605575 | AACTCTCCTGTGTCC[A/G]GCTGCCTTCTTTCCA | 57799 |
| rs553632884 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593264 | TTTCCCAAGGGGGCT[A/G]TTCAGGGTCTCAGAA | 57799 |
| rs553788570 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RAB40C | GRCh38.p7 | 16:610998 | GGTATCCATGGGGAC[A/G]TTGTTTCATAGTCTT | 57799 |
| rs553847474 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:622209 | CTTCTGGGAATTTAT[C/T]GTGTAGGTCGAGTTG | 57799 |
| rs553851853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:616459 | TTCTCCTGCCTCAGC[C/T]TCCCGAGTAGCTGGG | 57799 |
| rs553859744 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:621681 | TGGGTCACCCAGGTG[C/T]AGGTCCCTTGGTGTG | 57799 |
| rs553982529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:626303 | CCTCGGGGGAGAGGC[A/G]GCAGCACTGGGGGGC | 57799 |
| rs554003091 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:591714 | CCCCTGTCTCAGCCT[A/C]CCGAGTAGCTGGGAC | 57799 |
| rs554067616 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:617516 | GTGGTGGCTGTGAGC[C/T]CCTTCCCTCCCCTTC | 57799 |
| rs554130630 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:613394 | AGGGACTGCCGCCCT[C/G]GCCTGTAGAATCAAG | 57799 |
| rs554139778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596362 | TCCCTGAAAAGCTGC[C/T]GCCTACCCTGGTCTG | 57799 |
| rs554145169 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:609743 | AGCCATAGAAGGGCT[A/G]GAAAAGAAAGTTGAG | 57799 |
| rs554256804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:625723 | GCTACGGGGCCACCC[A/G]GAAGGGCTGCACTGT | 57799 |
| rs554381244 | snp | A/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:608392 | GCCAAATCTTATCAC[A/T]CCTGAGCCTGCTTAG | 57799 |
| rs554392573 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:601102 | TGTAGTTTTCCTCAC[C/T]GTTCAGTAAATGGGC | 57799 |
| rs554400844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:615050 | TTGGAAACGAGGACC[C/T]GAGGGAGACCATCCG | 57799 |
| rs554406872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596671 | GACTGTGGAACTGGC[A/G]GGTGTCAGGGACCAG | 57799 |
| rs554432908 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594359 | GGAGGGAGGCGGTTG[C/T]GGACATGGCGAGGCT | 57799 |
| rs554443111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:601506 | CTCCGGGCAGGTCCC[C/T]GCCGCAGCCGCGTCA | 57799 |
| rs554516833 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:606688 | AAGCCGAGCCTTTCC[C/T]GGCTTCTCCAGGCCG | 57799 |
| rs554545660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597168 | GTTCTAGTGCTGGTG[A/G]TGAGGTGGGTGGTGG | 57799 |
| rs554631634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:617583 | TGTGGTGGCTCACGC[C/T]TGTCATCCCAGCACT | 57799 |
| rs554633053 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:616788 | GTGGAAATAAAGGCA[C/G/T]TGCCCTTTCTCCAGG | 57799 |
| rs554634553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:626898 | AGCGGAGATCGTGCC[A/G]CGGCACTCCAGCCTG | 57799 |
| rs554655952 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:611988 | AGGGACAGCCGCCCT[G/T]GCCTGTAGAATCAAG | 57799 |
| rs554767388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622507 | CTAGAGCACTCGCTC[A/G]TTCTTTTGTTTTGTT | 57799 |
| rs554791375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:621208 | AGGCGGGCCTCTGAC[C/T]GCCGTGACTGAGCAT | 57799 |
| rs554830219 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:626352 | CCCCCCTCAGGGTGC[C/T]GCCGTGGCCGCTGCA | 57799 |
| rs554854717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:613841 | TGGGCAGCACCCAGG[C/T]CTAGACTTGGGTGAC | 57799 |
| rs554914942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:607724 | TGAACCCAGAAGGCG[A/G]AGCTTGCAGTGAGCC | 57799 |
| rs554943704 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:604927 | AGCCTGGTGTGGTGG[C/T]GGTGCTTGTGGTCCC | 57799 |
| rs554944661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:599346 | GCCACAGCCCTAGTG[A/G]CTGCCCGCAGAGTCT | 57799 |
| rs554977045 | snp | A/G | | | intron-variant, upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589581 | TAGCAGAGCCGTGAT[A/G]GACATGCAAGCGACC | 57799 |
| rs555028993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:623579 | GAATGGCGTGAACCC[A/G]GAAGCGGAGATCGTG | 57799 |
| rs555042001 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:620097 | TGGGCCCTGCCTGCT[A/G]TTGAAAGAGGAGTTG | 57799 |
| rs555057691 | snp | A/G | 0.0252325 | 0.109451 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589174 | AGCTGTGGCGGCCGC[A/G]TCCCCGGGCGGAAGG | 57799 |
| rs555177847 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RAB40C | GRCh38.p7 | 16:620505 | CATATACTATTTTGG[A/T]ATTAAAAAATATGGG | 57799 |
| rs555178113 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:615416 | ACTCCGTGGGAGGGC[A/G]TCGCTTATGTTTAAA | 57799 |
| rs555226852 | snp | C/T | 0.000163975 | 0.0090532 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629670 | GGTGTCTGCTATGCC[C/T]GGCCCAGGGGGGTGT | 57799 |
| rs555258612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:607312 | GACCAGCCTGGCCAA[C/T]ATGGTGAAACCCCAT | 57799 |
| rs555332083 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594569 | TGAAGTTCGTGGCTC[C/T]GAAGTGGCCAATTCC | 57799 |
| rs555599342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:609889 | GGGGAGCTGAGGCAC[A/G]TCAGGATGTGTCTCC | 57799 |
| rs555752311 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589886 | GGAGGGCGGCGGGCG[A/G]CCTCTGGTGACTACG | 57799 |
| rs555752411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595081 | GCCTCGGGGGTTTTG[C/T]TCGTTTTCTGGGGCA | 57799 |
| rs555774375 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:621538 | CCCGCGGCTCTTCCC[A/G]CGAGGCCCTTCACGT | 57799 |
| rs555775240 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:600001 | AGGTTTTGTTCCCTC[A/G]TGGCATCAGTCAGCG | 57799 |
| rs555790419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:625781 | CTTGACCTCCGCCCA[C/T]CTTGACCTCCCACGG | 57799 |
| rs555822898 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:591519 | TGCTGAGGGAGTCAA[C/T]GCTTTGTGCTAGAAG | 57799 |
| rs555834093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:615928 | GATTGTGGCACTGCA[C/T]TGCAGCCTGGGCGAC | 57799 |
| rs555861104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595251 | GCTTTCCGCTGCCCC[C/T]GTGTAGCCCCCACCA | 57799 |
| rs555966038 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:600719 | TTTGCACCACTACAC[C/T]CCAGCCTGGGCGACA | 57799 |
| rs555968869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:610003 | GAATGGGTCCCACGG[A/G]AGGGTGGGGATGTGA | 57799 |
| rs556000039 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595809 | GGTTTCACTGTGTTG[G/T]CCAGGCTGGTCTTGA | 57799 |
| rs556056280 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:610802 | TTGAGACCTTCCAGG[C/G]CAAGGGCCCCCTCCC | 57799 |
| rs556089326 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:624789 | CGCCCGACAGGGCTC[G/T]GAGTGTGAGCAGTGT | 57799 |
| rs556093798 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:620926 | TTTCTGTTCAGCTGC[A/G]TGAGAACTAAAAAAG | 57799 |
| rs556115193 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:616322 | TCAGTCCAGAGTCCG[A/G]AGAAGCAGCATTTTA | 57799 |
| rs556200937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:605169 | GTTGGAGGCTGCAGC[A/G]AGCCGTGATTGTTCC | 57799 |
| rs556206388 | in-del | -/GAGT | 0.00159617 | 0.0282053 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588861 | AAGCTCACCCGTTCC[-/GAGT]GAGTAACTTCACCGA | 57799 |
| rs556248685 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:625591 | AGGCTCTGGATTCCC[A/G]CCTGCCGCCCCTCCT | 57799 |
| rs556268558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:600919 | GTCACAACTGTGGCA[A/G]AGCCTGGTGTGTGGC | 57799 |
| rs556327361 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:590964 | ATCTGGGGTCCGGGG[A/G]AAGATGTCATGGTCC | 57799 |
| rs556378070 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:605522 | TGTGGACTCATCTGC[C/T]TTGTCTAGTTTTCAC | 57799 |
| rs556579828 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595896 | GTGAGCCACTGTGCC[C/T]GGCCTCTAATTGTGC | 57799 |
| rs556615795 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627841 | GCTGCTGGTGCTTCC[A/G]GGAATCTTGGTCGGA | 57799 |
| rs556664847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:590994 | CCGGTAGAAGGCGTC[A/G]TGGGCCAAAAGGAAG | 57799 |
| rs556730782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:602587 | GCACCTGCCACCACG[C/T]CCGGCTAGTTTTTTG | 57799 |
| rs556807947 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:591258 | ATCATCTGGGGTCTG[A/G]GGGAAGGTGTCATAG | 57799 |
| rs556874110 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588299 | CCTCTGAGCAGAAGA[C/G]GCTCTCCCTGACCCG | 57799 |
| rs556889559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:611445 | GTCAGCCTCATGGGG[A/G]CTTCAACAGCCAGGA | 57799 |
| rs556903567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:603095 | GGGGCCAGACCTGTG[C/T]TTTTTGTTTTCTTAA | 57799 |
| rs556982055 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RAB40C | GRCh38.p7 | 16:618885 | GGGGGCACTGGGGCC[A/T]TGTGTGCAGTGTGTG | 57799 |
| rs556983231 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:598024 | GGCCAAGGTGGGTGA[A/G]TCACGAGGTCAAGAG | 57799 |
| rs557065173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593118 | CTGGGCTGTGGAACG[C/T]GCTTTCTGTGTCTAA | 57799 |
| rs557162405 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:616321 | GTCAGTCCAGAGTCC[A/G]GAGAAGCAGCATTTT | 57799 |
| rs557203809 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594596 | TTCCAGGGGACACTA[C/T]CTTGAGAGGCTCCTC | 57799 |
| rs557203922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593654 | AACAAATGAGTCATC[A/G]AAGTGACCTTTTTCT | 57799 |
| rs557227683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:623476 | AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAA | 57799 |
| rs557244629 | in-del | -/A | | | intron-variant | RAB40C | GRCh38.p7 | 16:599736 | AGTCAGCGTGGATTC[-/A]GCAAGGTTTTGTTCC | 57799 |
| rs557250080 | snp | C/T | 0.0146672 | 0.084371 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589020 | TGCGGCAGCCGGGCC[C/T]GGCAGGGACGAGGGC | 57799 |
| rs557285813 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RAB40C | GRCh38.p7 | 16:614351 | CTGCCGCATCCCGAT[A/G]GTGAACTGCCAAACT | 57799 |
| rs557303933 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627892 | CTGCCTGGGCTTGAC[C/T]GGCGGGGAGCCTGGT | 57799 |
| rs557418039 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:614678 | AACTTTACCTCGTCC[C/T]GATGGTGAACTGCCT | 57799 |
| rs557430748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:623506 | AAAATACAAAAAAAT[C/T]AGCCGGGCATGGTGG | 57799 |
| rs557443228 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628433 | CTTGATGGGCAGCGG[C/T]GCAGACCCCGGGCAC | 57799 |
| rs557444639 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:609258 | TCAGGGCAGTGCCTG[C/G]TGTGGTTCCCAGCAG | 57799 |
| rs557452003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593742 | CCTGTGAGCTCTTCC[A/G]TGTCTCCTAATGTGG | 57799 |
| rs557515978 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:599393 | CTGCCTGAGAGGAGC[C/T]GCCAGGTCAGCTGAT | 57799 |
| rs557572376 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RAB40C | GRCh38.p7 | 16:604449 | TTTCTCTAGAATATA[C/T]GTGAGTCCTTCTGAA | 57799 |
| rs557717740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:598959 | TTCCCTGCCCGGGGC[C/T]GGCGGCTGCTGCTGG | 57799 |
| rs557726488 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628947 | GGGCACCAGTGGACT[C/T]GCCCCATGGCCCGTT | 57799 |
| rs557820008 | snp | A/G | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628063 | CTCGAGAGGGGACTC[A/G]CGGCCGCGATGGCAA | 57799 |
| rs557907275 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:608635 | AGCACTTTAGGAGGC[C/T]GAGGCAGGCAGATCA | 57799 |
| rs558053347 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RAB40C | GRCh38.p7 | 16:619961 | CGGAGATGTTGGCAG[C/T]TCCCTCATGGGAGCA | 57799 |
| rs558058562 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:590500 | GCTGGGCACGGAGCT[C/T]GCCCTCGGCCCGGCC | 57799 |
| rs558075072 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594648 | GTCGTCGGCTGCTTA[A/T]CCCCAGGGCTAGCTG | 57799 |
| rs558136629 | in-del | -/GCGACTTT | 0.00119737 | 0.0244387 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589227 | TGTCCCAGAACCTCA[-/GCGACTTT]GCAGACTCACTGGTG | 57799 |
| rs558210757 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:611025 | TCTTCTTACACTTTT[C/T]CTCTTCACTGTTGCT | 57799 |
| rs558252211 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:605026 | TCATGCCACTGCACT[C/G]CAGCCTGGGCGACAG | 57799 |
| rs558300700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629507 | CCGGTGGATGGAATC[C/T]CAGCTGGGCTGTGCT | 57799 |
| rs558345302 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:620359 | GATTGTGCCATTGCA[C/T]GCCAACCTGGGCGAC | 57799 |
| rs558400310 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:592343 | TGGACTGAGGCTGAG[C/T]GCGCTTCCTCCTGGC | 57799 |
| rs558456900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597334 | CCCCTGAGCAGCCTT[C/T]GCCGTCTTTACAGTG | 57799 |
| rs558490056 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | RAB40C | GRCh38.p7 | 16:620730 | ATCCCAGCCCCCCGC[C/T]GACGGGCTCCACCGC | 57799 |
| rs558516372 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:601994 | AGCGGGGTGTGGTGT[C/T]GGGCACCTGTAATCC | 57799 |
| rs558563245 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:618482 | GCAGCCTCCCCCTCC[C/T]GGGTTCAAGCGATTC | 57799 |
| rs558616118 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:612650 | CGCCTTTGCCTGTAG[A/C]ATCAAGAGCAGGGAC | 57799 |
| rs558640338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:607178 | CACGTCCACTCCCCA[A/G]ACCACCAGCACGTTG | 57799 |
| rs558684988 | in-del | -/CAGCCCC | 0.0106323 | 0.0721327 | intron-variant | RAB40C | GRCh38.p7 | 16:603774 | CAGGCCCTGCCGAGT[-/CAGCCCC]CAGCCCCCAGCAGTC | 57799 |
| rs558703778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:606754 | AGAGCCAGCACTGGC[A/G]GGTGAAGTCCCTCTC | 57799 |
| rs558714639 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:608038 | CCTGGGCAGCCTCCA[C/T]GCCCATGTACTCACC | 57799 |
| rs558759062 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:598849 | GTAAGAACCTCATGT[C/T]AACCCTGAGTGAAGG | 57799 |
| rs558802939 | in-del | -/AATA | | | intron-variant | RAB40C | GRCh38.p7 | 16:603641 | AGATGATGTCTATTT[-/AATA]AATGTACCCTCTTTG | 57799 |
| rs558804794 | snp | A/G | 1.7644e-05 | 0.00297013 | intron-variant | RAB40C | GRCh38.p7 | 16:618165 | CCTCTCACAGGGACC[A/G]CAGTCCCGGCCCCTC | 57799 |
| rs558842114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:608000 | CAACGTGCTGTGCCC[A/G]TCCCCACCTCCCTCC | 57799 |
| rs558887957 | snp | C/T | 1.77694e-05 | 0.00298067 | intron-variant | RAB40C | GRCh38.p7 | 16:627297 | TCCCTGCACAGGGCC[C/T]CCTCCCCCACAGCCC | 57799 |
| rs558902108 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:626916 | GCACTCCAGCCTGGC[A/G]ACAGAGCGAGACCCG | 57799 |
| rs558945299 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:617660 | CAAGCCTGGCCAACA[G/T]GGTGAAACGCCATCT | 57799 |
| rs559025462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622761 | CGCCTGCCTCGGCCT[C/T]CCAAAGTGCTGGGAT | 57799 |
| rs559063361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622548 | CGGTCTGGCTCTGTC[A/G]CCAGGCTGGAGTGCC | 57799 |
| rs559074243 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:609888 | GGGGGAGCTGAGGCA[C/T]GTCAGGATGTGTCTC | 57799 |
| rs559147401 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:591922 | TTTAACTTCCAGTGG[C/T]ATGGCTAAAATACAC | 57799 |
| rs559223498 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:626429 | GTGCTCGCTCCTTCC[C/T]GGTTCCGGGGCTGGT | 57799 |
| rs559256326 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:626216 | GGGCCAGTGAGGGAG[A/G]TTCAGGCAGGTCCCT | 57799 |
| rs559372316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:602674 | CTGACCTCAAGTGAT[C/T]CACCCACCTCGGCCT | 57799 |
| rs559372324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597793 | CTGTGCCCAGCCCAG[C/G]TCAGCATCTTTGGAA | 57799 |
| rs559386103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:613606 | GTGGAATGCCTTTTC[A/G]CTGCTTCTTGGTCGT | 57799 |
| rs559414176 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628824 | TGTCCTCAGGCCGTG[C/T]GGCACGACATGGCCA | 57799 |
| rs559431795 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:601704 | CACAGGACCGGGTGC[A/G]GTGGTGCACGCCTAT | 57799 |
| rs559433210 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:602367 | TCTAGTGATCCTCCC[A/G]CCTCAGCCTCTCAAG | 57799 |
| rs559479444 | in-del | -/A | | | intron-variant | RAB40C | GRCh38.p7 | 16:617850 | TCCGTCTCAAAAAAG[-/A]AAAAAAAAAAAGCAT | 57799 |
| rs559491976 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587514 | TGCTCGGAGGCTGGG[A/G]GGTCAGAGGGCACAG | 57799 |
| rs559498400 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:598605 | AAATTAGCTGGGTGT[C/G]GTGGTGCACGTCTGT | 57799 |
| rs559559567 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:598073 | AACATGATGAAACCC[C/T]GTCTCTACTAAAAAT | 57799 |
| rs559593995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:618535 | GCTGGGAGTACAGGC[A/G]CAGTGGGTGTACTTG | 57799 |
| rs559696642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:617715 | AGGTGTGGTGGCGGG[C/T]GCCTGTAGTCCCAGC | 57799 |
| rs559776207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:605256 | TGCTCAAGCAGCCCC[A/G]TTGTTTCATAGTCCC | 57799 |
| rs559821801 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:607761 | GCGCCACTGCACTCC[A/C]GCCTGGGCGACAGAG | 57799 |
| rs559834540 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:622989 | GGTCATTTGGGTCCC[C/T]GCGGCCTCACTGTGA | 57799 |
| rs559837428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:604752 | TGAGAACTCGTTGCT[A/G]TAAACATATTGAAAA | 57799 |
| rs559946670 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | RAB40C | GRCh38.p7 | 16:618069 | CAAAGCCGCTTAGCA[C/T]AGCCTCATTGGCACC | 57799 |
| rs559957595 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:600113 | TTTCCTGTTTGGTTT[C/G]GGACTCCCATGGCCC | 57799 |
| rs559975745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:623372 | AAATCATGCTGGGCC[A/G]GGCGCGGTGGCTCAC | 57799 |
| rs559998190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:625634 | CTGCACCCTGCACTG[C/T]CCCACGGCCTACGCC | 57799 |
| rs560011177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:610063 | GGCCAGGGCCAGATG[C/T]AGCCTCATACCAGCC | 57799 |
| rs560070497 | in-del | -/TTGCCATGCGGGAGG | 0.00279162 | 0.0372561 | intron-variant | RAB40C | GRCh38.p7 | 16:624182 | TTCTGAGTTGTGGGC[-/TTGCCATGCGGGAGG]TTGCCATGCGGGAGG | 57799 |
| rs560113683 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | RAB40C | GRCh38.p7 | 16:600420 | TGGATGTCACCTAAC[C/T]TGCCGAGTTTAAAAC | 57799 |
| rs560269213 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:622077 | GAAGGGGCATGTGTT[C/T]GTCAAAATTCATCAA | 57799 |
| rs560273791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595371 | GGGAGGAGCCGCCCT[A/G]CAGGCCTCCTGTGAA | 57799 |
| rs560291235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:591059 | AAAGGTGTCATAGAT[C/T]TGGGGGAAGGCATCA | 57799 |
| rs560363128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:590594 | GTGGCTGCGGGGTGC[C/T]CGTGCTCCAGTCCCG | 57799 |
| rs560468774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622792 | CGCAGGCGTGAGCCA[C/T]GGCGCCTGGCCGAAG | 57799 |
| rs560511238 | snp | A/T | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594838 | TTTTTTTTTTTTTTT[A/T]AGACGAAGTCTTACT | 57799 |
| rs560556837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:611482 | TGACCAAGGCCCCTC[C/T]GTCCCTGTGTCCCTG | 57799 |
| rs560610082 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:600661 | CAGGCTGAGGCAGGA[C/G]AATCGCTTGAACCTG | 57799 |
| rs560634876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:611117 | ACGCAGACGTCCAGC[A/G]GGAGGAGCATCCCAG | 57799 |
| rs560645099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:616582 | CGACCTCATGATCCG[C/T]CCGCCTCGGCCTCCC | 57799 |
| rs560673147 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:600157 | GCCTCTTCAGGTGGC[A/T]CCTGCGTCCTGGGCT | 57799 |
| rs560703056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:605763 | GTGAGGAGTCTCAGA[C/T]GCGTTTGGTCAACAC | 57799 |
| rs560734775 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596399 | CTGCGAGCTGGCGTA[G/T]AGCAGGAAGGGGTTG | 57799 |
| rs560746507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:611064 | TGTTCTGACGCGCAC[C/T]GTGGGCAACCGGGTG | 57799 |
| rs560790601 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RAB40C | GRCh38.p7 | 16:606367 | AGGTGTTGGCTGACA[C/T]GCAGTCCTCTCGGTC | 57799 |
| rs560914875 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:616981 | TGGACCACGCTCCTG[C/T]CCTGCCCTGCCCCGC | 57799 |
| rs560998540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:591448 | GGACCCTGTCTCGAG[C/T]GTGCACAGATGACAG | 57799 |
| rs561006730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:621813 | CTGTGGCCAAGTGCC[A/G]TGTCTGCTTCAGGAC | 57799 |
| rs561016449 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:592317 | GGGGGTTGGCAGAGC[A/G]TGGGATTACCTGGAC | 57799 |
| rs561089125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:625646 | CTGTCCCACGGCCTA[C/T]GCCTGGGCATGCTGG | 57799 |
| rs561152798 | in-del | -/CAGCCCC | 0.37878 | 0.214279 | intron-variant | RAB40C | GRCh38.p7 | 16:603780 | TGCCGAGTCAGCCCC[-/CAGCCCC]CAGCCCCCAGCAGTC | 57799 |
| rs561184275 | snp | C/G | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597025 | TTGGCGCTGTGGAGA[C/G]GTAGGGACCCATGGG | 57799 |
| rs561351666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:606912 | TCCTGTCTGCAGAGT[C/T]CCATGCTAGCAACTC | 57799 |
| rs561450441 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RAB40C | GRCh38.p7 | 16:614428 | AACTGCCTAACTCTA[C/T]CGCATCCCGATGGTG | 57799 |
| rs561450476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:619678 | ATGTGGGCCCAGGGA[A/G]GCCGCCTGGGTCTGG | 57799 |
| rs561468053 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:624861 | GATATTTAGGGCAGG[C/T]GGAAACAGCCCAGAG | 57799 |
| rs561526134 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596939 | GCTGTCTCGTGCTGA[C/G]ATCAGGATTTTGAGT | 57799 |
| rs561563623 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:622306 | CAGTTCACGAGCAGG[C/T]GGGGGTGCTGGGCCT | 57799 |
| rs561588722 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:602122 | CAGCTCTCAAAACAA[A/C]ACAAAAAACTACTGA | 57799 |
| rs561726184 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588555 | CTGGTGCGTCGATGT[A/G]GTCGCCGCTTAGTCA | 57799 |
| rs561760468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:603815 | TCCATCACATGGGCT[A/G]CTTTTTCCTGTTCCA | 57799 |
| rs561781131 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:607037 | CTCCACTCAGGTGGC[C/T]GAGGGTCCCACTTCC | 57799 |
| rs561797261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:604520 | TTCTCTAGAATACAC[A/G]TGAGTCTTTCTGAAG | 57799 |
| rs561926613 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:599208 | CCAGGCCCCGGCCCC[A/G]GCCGAAGCTGCCACT | 57799 |
| rs561945231 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:608824 | GTTGCCATGAGCCAA[C/G]ATTGTGCTACAATTG | 57799 |
| rs562028101 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:604297 | TCATTTTAGCCATAT[G/T]TAGGGATACAGTTCA | 57799 |
| rs562039422 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594718 | ACTGGACAGCCGTGC[A/G]TGGCTTCCCTGTGCC | 57799 |
| rs562103318 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:599530 | GGCATGTACGTGAAA[A/G]TGCACACCCGTGGGT | 57799 |
| rs562110732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:615048 | TCTTGGAAACGAGGA[C/T]CCGAGGGAGACCATC | 57799 |
| rs562146765 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:590523 | GCCCGGCCCTTCCAA[G/T]CGCCGCCGAACGTTC | 57799 |
| rs562176124 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | RAB40C | GRCh38.p7 | 16:590219 | CAGGTGCGGGGCGCG[G/T]GCTCTCTCACGCCGC | 57799 |
| rs562228047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:615682 | ATGATGTGATGTGGG[C/T]CGGGCACGGTGGCTC | 57799 |
| rs562228133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:620813 | GCCGACGGGCTCCAC[C/T]GCGGGCATCCCAGCC | 57799 |
| rs562249266 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:609009 | AGTCCCAGCTACTCA[G/T]GAGGCTGAGCTATGA | 57799 |
| rs562368377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:616038 | TGAGGCGGGTGGATC[A/G]TGAGGTCAGGAGATC | 57799 |
| rs562490665 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629240 | CTCCGAACCGTTCTT[C/T]GTACAGTAAATGTAA | 57799 |
| rs562516053 | snp | C/T | 0.000741977 | 0.0192468 | intron-variant | RAB40C | GRCh38.p7 | 16:625063 | GTACTCCCGGGGGGA[C/T]TCACTGATGGACTGG | 57799 |
| rs562851724 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:590542 | CGCCGAACGTTCCCA[G/T]GAACGCCTTTGCCTG | 57799 |
| rs562914613 | snp | A/G | 0.00119976 | 0.024463 | intron-variant, utr-variant-5-prime | RAB40C | GRCh38.p7 | 16:590245 | GCCGCGGCCTCACCC[A/G]GCGGTGCTTCGGCAG | 57799 |
| rs562916619 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595293 | AAGGCAGCACCACCC[C/G]CACTGTGCAGACGAG | 57799 |
| rs562916696 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:622660 | CTAGGTGTGCACCAC[C/T]GCGTCCAGCTAATTT | 57799 |
| rs562972898 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:616523 | TTTTGTATTTTTAGT[A/G]GAGACGGGGTTTCAC | 57799 |
| rs563009350 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:620837 | CCCAGCCACCCCCCC[C/T]GACGGGCTCCACCGC | 57799 |
| rs563168941 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:605684 | TCAAGGCTGCAGTGC[A/G]TTGGCTCCACTCCAG | 57799 |
| rs563261051 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:592661 | CTCCAGGGGCGCTGC[A/G]CACTCCCAGGAGGCT | 57799 |
| rs563321048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597506 | TTTTATTTTTTGAGA[C/T]AGAGTCTTGCTCCGT | 57799 |
| rs563321371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:592079 | TGTGGCCCCAGATGA[A/G]CTGGGAGCAGTCAGC | 57799 |
| rs563351755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:617837 | GACAGAATGAGACTC[C/T]GTCTCAAAAAAGAAA | 57799 |
| rs563376165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622868 | AGTGGAAGAGTCTGT[C/T]TGTCCCGTGCTCTGC | 57799 |
| rs563381138 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:591949 | ACACTAGATAGGTGG[C/T]ATCACTGGGGCTTGC | 57799 |
| rs563414855 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:611547 | AGGGTGTTGACGGCC[G/T]GAGCGCGGTGCCTCC | 57799 |
| rs563416333 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:603799 | CCCCCAGCAGTCGGC[-/T]TCCATCACATGGGCT | 57799 |
| rs563442169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:613649 | TTTGGGGAAATGTCT[A/G]TTCAAGTCCTTTGCC | 57799 |
| rs563465988 | snp | A/G | 1.67377e-05 | 0.00289284 | intron-variant | RAB40C | GRCh38.p7 | 16:618297 | CCATTGCTTTTCAAA[A/G]GATGTTTCTCCTGAT | 57799 |
| rs563508386 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587932 | TCTGCCTCAGCCTCC[C/T]AAGTAGCTGGGATTA | 57799 |
| rs563522297 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588750 | ACGTGACGGGCTCCG[C/T]ACCCGGTCTGGAGAG | 57799 |
| rs563525734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594322 | TCCGGTCCTTTGAGC[C/T]TGGCAAGTTGTGGGG | 57799 |
| rs563566020 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:602751 | AAATTATTTTTTGTA[G/T]AATTGAGGTCTTGCC | 57799 |
| rs563566942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:607806 | AAAAACGAAAAGAAA[A/G]GAAAAGAAAGTCGCA | 57799 |
| rs563579154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:614039 | TGCCTAACTCTACCG[C/T]GTCCCGATGGTGAAC | 57799 |
| rs563585025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593952 | GGGTGGTGCACGCGG[C/T]GGGGAGGAGAAAGCT | 57799 |
| rs563597554 | in-del | -/TG | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:626489 | CCTGCAGCTTTGTGT[-/TG]TGTCATCTGCTCTTC | 57799 |
| rs563613422 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589228 | GTCCCAGAACCTCAG[A/C]GACTTTGCAGACTCA | 57799 |
| rs563743057 | snp | C/G/T | 0.0154538 | 0.0865337 | intron-variant | RAB40C | GRCh38.p7 | 16:620998 | CCTGGAAAGCAAGCT[C/G/T]TGTTATCATCTCCGT | 57799 |
| rs563758005 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628060 | CTCCTCGAGAGGGGA[C/T]TCGCGGCCGCGATGG | 57799 |
| rs563761167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:598695 | TGCAGTGAGTCTGAC[C/T]GTTGCACTACGTTCC | 57799 |
| rs563868809 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:619205 | TGCACTCAGGGCCAT[A/G]TGTGTGTGCAGGCAT | 57799 |
| rs564021746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:614068 | ACTGCTAACTCTGCC[A/G]TATCCCGATGGTGAA | 57799 |
| rs564033999 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:618451 | CTGGAGTACAGTGGC[A/G]CAGTCTCGGCTCACT | 57799 |
| rs564050778 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:623793 | CTCTAAAAAATGTTT[A/T]AAAAAACTTAGCCAG | 57799 |
| rs564074438 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587644 | AACCTGACTTCTTCA[A/T]CAGCCAGGGGATGAC | 57799 |
| rs564241045 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:604887 | CAACATGGTGAAACC[A/G]TATCTCTACTAAAAA | 57799 |
| rs564309231 | snp | A/G | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593953 | GGTGGTGCACGCGGC[A/G]GGGAGGAGAAAGCTG | 57799 |
| rs564331497 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:603690 | GAGTTTTGGCACATA[C/T]ATGTACCTATGCAGC | 57799 |
| rs564332017 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589998 | TCGTGACGGACGGGC[G/T]GGTGGGCCAATGGGC | 57799 |
| rs564338460 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RAB40C | GRCh38.p7 | 16:614376 | CAAACTTTACCTCGT[C/T]CCGATGGTGAACTGC | 57799 |
| rs564344199 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589353 | CACCGCCTTAGAGAG[A/G]ACGCGCCCGGGGCCA | 57799 |
| rs564394676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:608275 | CTCACTCACCCGCAC[A/G]AAAACAGCAGGGGGG | 57799 |
| rs564485967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:599160 | TTCGGTCCAGAAAGT[C/T]ACTGCTGCAGGGGAG | 57799 |
| rs564553980 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:623989 | CGTTCTTACCTCACC[A/T]GGGTTGCACATCTCT | 57799 |
| rs564572794 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594382 | GCGAGGCTAACATCA[C/T]GGTTTGCTGTGGATG | 57799 |
| rs564637491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:615085 | TCCTAAAATTGGGAC[A/G]TTTGGTTTTCTGTTG | 57799 |
| rs564640476 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:624205 | CGGGAGGTTGCCATG[A/C]GGGAGGTTGCCACTA | 57799 |
| rs564647328 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628595 | GTCCACGTCCACGTC[A/C]ACCTGGGGGCCTCGG | 57799 |
| rs564679936 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:617067 | CCGAGATTTCCCCCT[A/G]CCCCACTGGCTGAGT | 57799 |
| rs564713991 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RAB40C | GRCh38.p7 | 16:600683 | TTGAACCTGGGGAGG[C/T]GGAGGTTGCAGTGAG | 57799 |
| rs564721639 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:591846 | ATGATCTGCCCACCT[C/T]GGCCTCCCAAAGTGC | 57799 |
| rs564800153 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:615611 | AGAACTGTCTGCTCC[G/T]TTCAGTTTCTCTTGG | 57799 |
| rs564809215 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RAB40C | GRCh38.p7 | 16:615266 | TGGTCAGGCAGAAGG[A/G]CGGTGTGGGTGGAAG | 57799 |
| rs564829093 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RAB40C | GRCh38.p7 | 16:592761 | CCAGGACATGAAGGC[A/G]TGCTTCTGAGGGCCG | 57799 |
| rs564848148 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:601137 | TGCTTGTGTTTGGAA[C/G]AGAGATAGAAGCTGT | 57799 |
| rs564921553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594462 | TGTACCCATGGGAGC[A/G]AGGGCACCCTGTGTG | 57799 |
| rs564927267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:600730 | ACACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC | 57799 |
| rs564959862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:626180 | GGCTGCCCTGATCAC[A/G]TGGAGGCTGAGGGGG | 57799 |
| rs564995461 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:607459 | AGTGAGCTGATATTG[C/T]GCCACCACACTCCGG | 57799 |
| rs564997899 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594414 | TGGGGCCTGGTGGTC[A/C]CTGAGATGTCTGTGG | 57799 |
| rs565011620 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596113 | TGCATGGCAGGTGCA[C/T]GGCAGTGCCAGCCAG | 57799 |
| rs565029650 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:617346 | AACCCTTAGAGAAAC[A/T]GGAAGGCGTCCTGTT | 57799 |
| rs565047835 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:626393 | CCTGTGGGTCCCTGG[C/T]ATTGCTGGTGTGGGC | 57799 |
| rs565191869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:617108 | TGCTTCTCCACTTCC[A/G]CGTGGGTCTTGGCCC | 57799 |
| rs565225604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622695 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 57799 |
| rs565280611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:627019 | GGGGATGAGTCAGGA[C/T]GCTTGAAGGGCCAGA | 57799 |
| rs565327533 | in-del | -/GCCGGAAGATTGAATGCGGAGC | 0.00795532 | 0.062565 | intron-variant | RAB40C | GRCh38.p7 | 16:603419 | CGAGGGGAGTGGTAT[-/GCCGGAAGATTGAATGCGGAGC]GCCGGCCCCGCACGT | 57799 |
| rs565335898 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | RAB40C | GRCh38.p7 | 16:601850 | AAAAAAAAAAAGGCC[A/G]GATGCGGTGGCTCAC | 57799 |
| rs565487984 | snp | C/T | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628589 | CACCTCGTCCACGTC[C/T]ACGTCCACCTGGGGG | 57799 |
| rs565519004 | snp | C/T | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596792 | TGGGTGGAAGAGGGG[C/T]CTCTTCAGTCCTCTT | 57799 |
| rs565630610 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:621519 | CCTGTCACACAGCAG[A/C]AGTCCCGCGGCTCTT | 57799 |
| rs565700464 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:611774 | AAGAGCAGGGACAGC[A/C]GCCCTGGCCTGTAGA | 57799 |
| rs565743792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:611370 | CACGTCGAGGTGACC[A/G]TCAAGGAGAAGCAGC | 57799 |
| rs565758727 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:617135 | GCCCTGGGAGGCCAG[C/T]GGCCGAGGCTGGTCT | 57799 |
| rs565772589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596636 | GCTGACTTCCTGGGC[A/G]GTCGGGAGAAGGATG | 57799 |
| rs565774352 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:601913 | TGGGTGGATCACGAG[A/G]TCAGGAGATTGGGAC | 57799 |
| rs565836849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:606628 | AGGTTGGCAGAATTC[C/T]GTTCTTGCTGGTGGT | 57799 |
| rs565886818 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:622727 | GCCAGGATGGTCTCC[A/G]TCTCTTGACCTCGTG | 57799 |
| rs566115742 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589133 | CCGGGTCTTGAGCTC[C/G]CGCCGGCCGCGCTCC | 57799 |
| rs566165706 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:604353 | CAAATACGCACGAGG[C/T]CTTCTGAAGGTGTTT | 57799 |
| rs566268820 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:610739 | CTCCTCCCTCTACCC[C/T]GCCCTGCCCCACCCC | 57799 |
| rs566281505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:627191 | GTGCTGGGCAGAGAA[A/G]TTTGGGCGTCCAGGT | 57799 |
| rs566309629 | snp | A/G | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587995 | GTATTTTCAGTGGAG[A/G]GGGGGTTATCACGAT | 57799 |
| rs566370478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:598980 | CTGCTGCTGGGCTTT[C/T]GCCTGACTTCCTGGT | 57799 |
| rs566525734 | snp | A/G | 0.000227596 | 0.0106652 | utr-variant-5-prime | RAB40C | GRCh38.p7 | 16:590277 | CGGCCGGCGCGGGGC[A/G]CAGGCGGCGCGGCCA | 57799 |
| rs566589906 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594907 | TCACTGCAACCTCTG[C/T]CTTCTGGGTTCAAGT | 57799 |
| rs566707855 | in-del | -/AAAG | | | intron-variant | RAB40C | GRCh38.p7 | 16:598755 | CAAAAAATAAAAAAT[-/AAAG]AAAAGAGGATGGAAG | 57799 |
| rs566735865 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:615862 | AGCTACTTGGGAGGC[C/T]GAGGCAGGAGAATCG | 57799 |
| rs566787162 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:600373 | TCATAATAATAGTAA[C/T]AGTAGCAAGTGCAAA | 57799 |
| rs566827791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:623466 | CATCCTGGCTAACAC[A/G]GTGAAACCCTGTCTC | 57799 |
| rs566863285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:610478 | CTGCACGGAGCAGCT[A/G]ACCTTCACTGGCGCC | 57799 |
| rs566983081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:605090 | AGCCTGGTGTGGTGA[C/T]GCACACTTGTAATAG | 57799 |
| rs567044860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595070 | GTGATCCACCTGCCT[C/T]GGGGGTTTTGCTCGT | 57799 |
| rs567095069 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:600453 | TGTTGTTGGACTTTT[G/T]TAAAGAGCTTTGGTG | 57799 |
| rs567166191 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595728 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 57799 |
| rs567184263 | snp | A/G | 0.000185816 | 0.00963708 | intron-variant | RAB40C | GRCh38.p7 | 16:625524 | GGTAGGCCTGGGTCC[A/G]GGGAGCCCTCCCGGG | 57799 |
| rs567201893 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:610699 | TCCAGGCCTCTCCTG[G/T]GTCACTGCTCTGTGC | 57799 |
| rs567203974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:616628 | CAGGCGTGAGCCACC[A/G]CGCCCGGCCAGAAGC | 57799 |
| rs567204818 | snp | A/G | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587575 | GGTTCCTGAACCCAG[A/G]AACCCAGGACAGGGC | 57799 |
| rs567267011 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:616273 | AAAAAAAAAAAAATA[A/C]CAATGTGGCAGGCAG | 57799 |
| rs567362442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:625179 | GATGGCTCCAGGGGA[A/G]GGAGGGGAAGCGGCA | 57799 |
| rs567381368 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:624764 | GAATGGGCCTGTGAT[G/T]TCACCGTTTCGCCCG | 57799 |
| rs567397758 | snp | C/G | 0.000328192 | 0.0128058 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629708 | CCGGAGGTCACAGCT[C/G]AGCTGGAACGGGGCA | 57799 |
| rs567470651 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RAB40C | GRCh38.p7 | 16:620506 | ATATACTATTTTGGT[A/G]TTAAAAAATATGGGG | 57799 |
| rs567618332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:605460 | CAGCCCTCGCAGCCT[C/T]GCCCTCTGCAGGCCT | 57799 |
| rs567650635 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:600867 | TGGGGAAACAGAAAG[G/T]TTTTGACTCCAGTCT | 57799 |
| rs567707922 | in-del | -/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628579 | TGCCTGGAACCACCT[-/C]GTCCACGTCCACGTC | 57799 |
| rs567753514 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:623415 | AGCACTTTGGGAGGC[C/T]GAGGTGGGCAGATCG | 57799 |
| rs567807697 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:625807 | CACGGCCCTCACCCC[A/T]TCATAGTCCAGACAA | 57799 |
| rs567892930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:626251 | AACGCGCAGTAGGGG[C/T]TCGGCCGGCGGCAGG | 57799 |
| rs567918952 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:591588 | TTTTGTTTTCTTTTC[G/T]TTTCTTTCTTTTTTT | 57799 |
| rs567979662 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:591231 | CTCAGGGGAAGGTGT[A/C]ATGGGTCTAGGATCA | 57799 |
| rs568013864 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:614101 | GCCGAACTCTACCGC[A/G]TCCCGATGGTGAACT | 57799 |
| rs568052971 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RAB40C | GRCh38.p7 | 16:616684 | CCCTAACACCAACCT[G/T]GGCAGTTCCTGGGCT | 57799 |
| rs568149405 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:607916 | AGACCCCTTCCTCCC[A/C]CTCCACTGCCCGTTT | 57799 |
| rs568150241 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627804 | ACCAAGCGCGGCAGG[C/T]GGGAGGAGGGGGCGC | 57799 |
| rs568159981 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:603013 | GATAGGGTCTCACTG[G/T]GTTGCCCAGGCTGGT | 57799 |
| rs568285741 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593550 | ACAGCTCCTTCAGCT[C/G]ACACCGGATCGCTTA | 57799 |
| rs568289898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:623175 | CTGAGGCAGCCCATC[A/G]GCCGGGAGGCGGGCC | 57799 |
| rs568298488 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:598335 | GTGAGCCGAGATCAC[G/T]CCACTGACTCCAGCC | 57799 |
| rs568348544 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-5-prime, upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589435 | GGGGCTTTCGTTTCC[C/T]GGACTCAGCCGCATC | 57799 |
| rs568387021 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:598912 | AGCAGCTCCAGCAGC[G/T]TGGGTAACCCGGTGG | 57799 |
| rs568411885 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:599360 | GGCTGCCCGCAGAGT[C/T]TTGCGCCCACCTGAT | 57799 |
| rs568421315 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RAB40C | GRCh38.p7 | 16:619399 | AGTGTGTGTGCAGGT[A/G]TGGTGGGTGCGCTTG | 57799 |
| rs568480503 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:608353 | TGTGGGGATTAGTCA[A/T]GGTGAGATTTGGGCG | 57799 |
| rs568543939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:615202 | TTTTTCTGTCCATTG[A/G]TGGTGTCCTTCGATG | 57799 |
| rs568587117 | in-del | -/T | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597473 | CAGCCATCTAGCATC[-/T]TTTTTTTTTTTTTTA | 57799 |
| rs568612334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:614599 | CCCGATGGTGAACTG[C/T]CTAACTCTACCACAT | 57799 |
| rs568649929 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:604879 | AGCCTGGCCAACATG[A/G]TGAAACCGTATCTCT | 57799 |
| rs568662151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:609777 | ATCTCCCAGAAAATA[A/G]AACAAAAAGAGATTA | 57799 |
| rs568669000 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627701 | ACGCCAGGCCAGTGC[C/T]GCCTACGTGGAGACT | 57799 |
| rs568673433 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628797 | ACAGCACTGGTGCTC[A/G]CCTCTACCTCCTGTC | 57799 |
| rs568707517 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629228 | ATTCCTGGTTCTCTC[C/T]GAACCGTTCTTTGTA | 57799 |
| rs568707775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:608292 | AAACAGCAGGGGGGA[A/G]CCACCCCCATGATTT | 57799 |
| rs568739077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:604433 | AGTCCTTCTGAAGGT[A/G]TTTCTCTAGAATATA | 57799 |
| rs568791769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:603199 | TTGTGGGTTTTAAGG[C/T]GTTAAGTAAAAGCTC | 57799 |
| rs568920341 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:623477 | ACACGGTGAAACCCT[G/T]TCTCTACTAAAAAAA | 57799 |
| rs568927578 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:598953 | GCTGCTTTCCCTGCC[C/T]GGGGCCGGCGGCTGC | 57799 |
| rs568939634 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:603947 | GGTATTCCTTTGCAC[A/C]AATATACCCCAGTTT | 57799 |
| rs568989424 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:599264 | CCACCAGCTTTGCTC[C/T]GAGGGGTGTCTGTGT | 57799 |
| rs569079284 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:619874 | TGTTGGATCTGATGT[C/T]TTCTACCTGCTGGCG | 57799 |
| rs569131531 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589590 | CGTGATGGACATGCA[A/G]GCGACCCAATGGCGC | 57799 |
| rs569383095 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:609311 | TGGGAAAATTGAGTC[A/G]TGGACAGCAGACACC | 57799 |
| rs569405910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:600312 | TAGCTAGTATGTCAG[C/T]TTCTTAAATTACTTT | 57799 |
| rs569504062 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:604990 | TTGAACCCGGGAGGC[A/G]GAGGTTGGAGTGAGC | 57799 |
| rs569588628 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:622441 | AACTGACTGTCAGGG[C/T]GGCTCCTAGAGGGGC | 57799 |
| rs569590887 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:607818 | AAAAGAAAAGAAAGT[C/T]GCATCTGGTAAAGCA | 57799 |
| rs569602082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629427 | CGGTTGGCTGGGTTC[A/G]CCTCAAAGTGAGGGC | 57799 |
| rs569710001 | snp | A/G | 7.53835e-05 | 0.0061389 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629456 | GCTGGAGCTGGGCTG[A/G]AGCAGCTGGGCCTGG | 57799 |
| rs569719310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:607164 | AGGGGCACAGGTGCC[A/G]CGTCCACTCCCCAGA | 57799 |
| rs569748743 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597876 | GAGGCCGAGGTAGGC[A/G]GAGTGCTGGAGCCCA | 57799 |
| rs569749887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:613360 | GGGGACAGCTGCCCT[C/T]GTCTTTAGATTGAAG | 57799 |
| rs569772374 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593366 | AGCTTTAGGCCTCTG[A/G]CCCTCGTGGGAAGGA | 57799 |
| rs569809102 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:611997 | CGCCCTGGCCTGTAG[A/C]ATCAAGAGCAAGGGA | 57799 |
| rs569834400 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:592961 | TGCCTGCTTGCAGAG[A/T]CTTCAGAGGCTCACA | 57799 |
| rs569859754 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:601982 | AATATAAAAGTTAGC[A/G/T]GGGTGTGGTGTCGGG | 57799 |
| rs569876893 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:607308 | TTGAGACCAGCCTGG[A/C]CAACATGGTGAAACC | 57799 |
| rs569904677 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:602026 | AGCTACTCAGGAGGC[C/T]GAGGCAAGAGAATCG | 57799 |
| rs569928081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:602455 | TTTTATTTTTGAGAC[A/G]AAGTCTTGCTCTTGT | 57799 |
| rs569994341 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RAB40C | GRCh38.p7 | 16:614526 | CAAACTTTACCTCGT[C/T]CCGATGGTGAACTGC | 57799 |
| rs570009933 | snp | A/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587744 | TTGTTTTTCTTTTTT[A/T]AAAAAGTTTATTTTT | 57799 |
| rs570020702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:614158 | GAACTGCTAACTACC[A/G]CATCCCGATGGTGAA | 57799 |
| rs570026294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:627265 | CCCCGCCAGGCTTCT[C/T]TTGGGCACCTCAGGT | 57799 |
| rs570096488 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:622750 | ACCTCGTGATCCGCC[C/T]GCCTCGGCCTCCCAA | 57799 |
| rs570108884 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:615736 | GGAGGCCAAGGCGGG[C/T]GAATCACCTGAGGTC | 57799 |
| rs570154729 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:613430 | GACTGCCGCCCTGGC[C/T]GGTAGAATCAAGAGC | 57799 |
| rs570171016 | in-del | -/G | 0.00517822 | 0.0506191 | intron-variant | RAB40C | GRCh38.p7 | 16:608284 | CGCACAAAAACAGCA[-/G]GGGGGGAACCACCCC | 57799 |
| rs570180155 | snp | A/C | | | intron-variant, upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589617 | GCGCCGGCGACGGGG[A/C]GGGCGAGGACAACGG | 57799 |
| rs570274762 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588061 | CCACCTCAGCCTCCC[A/G]AAGTGCTGGGATTAC | 57799 |
| rs570324673 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:613385 | TTGAAGAGCAGGGAC[A/T]GCCGCCCTCGCCTGT | 57799 |
| rs570401647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:617892 | TCAGCGTTGATGAGA[C/T]GTGAATGTCCACAGG | 57799 |
| rs570473646 | snp | A/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:622259 | GTGCTCAGATGCATA[A/T]TGCCACCGTTACCCA | 57799 |
| rs570559194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:607619 | CCACGGTGAAACCCC[A/G]TCTCTACCAAAAATA | 57799 |
| rs570573177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:607180 | CGTCCACTCCCCAGA[C/T]CACCAGCACGTTGAT | 57799 |
| rs570580272 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588786 | CGCTGGGTCGGCGCT[A/G]ACGTTACTGCTTTTA | 57799 |
| rs570669169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:597982 | CCGGGTGCAGTGGCT[C/T]ACACCTGTAATTCCA | 57799 |
| rs570679792 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:598277 | CAGCTACTTGGGAGG[C/G]TGAGGTACGAGAATG | 57799 |
| rs570688149 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:602472 | AGTCTTGCTCTTGTC[C/G]ACCAGGCTGGAGTGT | 57799 |
| rs570807642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:604039 | TAATGCTGATGTGAA[C/T]GAGTTCTTCTTTTTT | 57799 |
| rs570821733 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:608379 | GGGCGGGGACACAGC[C/T]AAATCTTATCACTCC | 57799 |
| rs570843759 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RAB40C | GRCh38.p7 | 16:614217 | GAACTGCTAACTCTG[C/T]CGCATCCCGATGGTG | 57799 |
| rs570866857 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593484 | CTGGGCAGTGGGTGC[C/G]CTTGGCAGGGAGGCC | 57799 |
| rs570878341 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RAB40C | GRCh38.p7 | 16:622609 | GCCTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC | 57799 |
| rs570890071 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:590821 | GTCTAGGATCATCTG[C/G]GGTCCGAGGGAAGGT | 57799 |
| rs570903106 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RAB40C | GRCh38.p7 | 16:618833 | GTAGTGGGTGCACTC[A/G]GCCATGTGTATGTGC | 57799 |
| rs570909684 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:619274 | AGTGTGTGTGCAGGT[A/G]TGGTGTACTTGGAGC | 57799 |
| rs570968021 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:591163 | GGTGTCATGGGTCTG[G/T]GATCTCAGGGGAAGG | 57799 |
| rs570997371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:614558 | TAAACCTCGTCCCGA[C/T]GGTGAACTGCCTAAC | 57799 |
| rs571053790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:609154 | CTGATAGGTGAGAGA[A/G]GTTTGATGGTTTGGG | 57799 |
| rs571143485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:627237 | CCTGGGAACACCTCT[A/G]GGAGTGTGGAGACCC | 57799 |
| rs571198580 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595474 | GCTTCTGCTGCACCG[C/T]GCACACTAAGTTCTC | 57799 |
| rs571204467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:611615 | CAGCCGCCCTGGCCT[A/G]TAGAATCAAGAGCAG | 57799 |
| rs571236913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:621499 | GCCACTCCCCGCTGC[C/T]GTCACCTGTCACACA | 57799 |
| rs571284455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629756 | ACCAGACCACAGCCT[C/T]TGGCTCAGGTGCCTC | 57799 |
| rs571339447 | snp | A/G | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595525 | GACCGCCTCAGGCCC[A/G]GGATGACCCTGGCTG | 57799 |
| rs571416186 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RAB40C | GRCh38.p7 | 16:625709 | CAGCAAGACCAGGAG[C/T]TACGGGGCCACCCGG | 57799 |
| rs571451972 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RAB40C | GRCh38.p7 | 16:603265 | GAATTTCTTCTGACA[C/T]TTGGCATGCTGGTGT | 57799 |
| rs571604955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596574 | CCTGGTGCGGAGAAC[A/G]CTGCCGAACCACTGT | 57799 |
| rs571666589 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:601368 | CCTAGGTGGGCTGGG[A/C]AGAAGGCTGTTCTGC | 57799 |
| rs571706871 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587561 | TCACCCTATGGAAAG[C/G]TTCCTGAACCCAGGA | 57799 |
| rs571784681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:605590 | GGCTGCCTTCTTTCC[A/G]TGTCTTCTGGGTGAG | 57799 |
| rs571834717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:617500 | CGGAAAACCTGATTC[C/T]GTGGTGGCTGTGAGC | 57799 |
| rs571849138 | snp | A/G/T | 0.00319098 | 0.0398384 | intron-variant | RAB40C | GRCh38.p7 | 16:592207 | CTTGGGCTCTTGTCC[A/G/T]TCCTGTCTGACTGCC | 57799 |
| rs572022822 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:607910 | ATTTTCAGACCCCTT[A/C]CTCCCCCTCCACTGC | 57799 |
| rs572086842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:611058 | GAATCCTGTTCTGAC[A/G]CGCACCGTGGGCAAC | 57799 |
| rs572169985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:605859 | TGCCAACCCGTTCTC[C/T]AAAGCAGTCACACAG | 57799 |
| rs572238173 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:616973 | ACACTGTATGGACCA[C/T]GCTCCTGCCCTGCCC | 57799 |
| rs572250570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596387 | GGTCTGGAGCCCCTG[C/T]GAGCTGGCGTAGAGC | 57799 |
| rs572384263 | in-del | -/GA | 0.00318978 | 0.0398085 | intron-variant | RAB40C | GRCh38.p7 | 16:604958 | GTTACTTGGGAGGCT[-/GA]GAGGCAGGACAATCA | 57799 |
| rs572385662 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:625795 | ACCTTGACCTCCCAC[A/G]GCCCTCACCCCATCA | 57799 |
| rs572524598 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:591717 | CTGTCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 57799 |
| rs572536513 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597231 | CTTACAGAGGGCTTG[A/G]TGCTGGGGGGCCTGG | 57799 |
| rs572633540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:623537 | CGGGCGCCTGTAGTC[C/T]CAGCTACTCAGGAGA | 57799 |
| rs572676767 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:607249 | ACCCTGTCATCCCAG[C/T]GCTTTGGGAGGCCGA | 57799 |
| rs572691329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:606885 | TCCCACCTCGAGATC[C/T]GTGCACCTTAATCCT | 57799 |
| rs572715507 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:619547 | GTCATGGCCACTGTT[A/G]TTGCTGCTTCAGTGG | 57799 |
| rs572760634 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:601714 | GGTGCGGTGGTGCAC[A/G]CCTATAATCCCAGCT | 57799 |
| rs572868011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594248 | TTAATCCTGGCTTGA[C/T]TTTATTTCTCTCTCT | 57799 |
| rs572945634 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:614910 | ATAGTGAACTGCCTA[A/T]CTCTACCGCATCCTG | 57799 |
| rs572984123 | snp | A/G | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594384 | GAGGCTAACATCACG[A/G]TTTGCTGTGGATGTT | 57799 |
| rs572988512 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588455 | TCGCTTGTGCCGGGG[A/G]GGTAGAGGCTGCAGT | 57799 |
| rs573094244 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:615401 | CCACTGGGCAGGTGC[A/T]CTCCGTGGGAGGGCG | 57799 |
| rs573129861 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:608701 | ATGGTGAAACCCCAT[C/T]TCTACAAAAAATGCA | 57799 |
| rs573171612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:599604 | GTGGCATCAGTCAGC[A/G]TGGATTCAGCAAGGT | 57799 |
| rs573236935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:604503 | AGTCCTTCTGAGGGT[A/G]TTTCTCTAGAATACA | 57799 |
| rs573252523 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629083 | CTTCCCTGTCCTGGC[C/T]CCACCTGTCCTGTTG | 57799 |
| rs573259784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:619703 | GTCTGGGTCTGGATC[C/T]TTCTTGGGGGAAGGT | 57799 |
| rs573361567 | snp | C/T | 0.00103824 | 0.0227606 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629543 | CTCGCTCACAGTCCC[C/T]GGCAGCAGATGGCCT | 57799 |
| rs573362047 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RAB40C | GRCh38.p7 | 16:599737 | AGTCAGCGTGGATTC[A/G]CAAGGTTTTGTTCCC | 57799 |
| rs573383840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595229 | TTGCCTGCCAGCACC[A/G]GTGGGCGCTTTCCGC | 57799 |
| rs573387003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:599477 | GCCACGCCGTGCCTC[C/T]TCCGTGTGCGCTGCT | 57799 |
| rs573420047 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:590000 | GTGACGGACGGGCGG[A/G]TGGGCCAATGGGCTC | 57799 |
| rs573468718 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:624884 | GCCCAGAGCTGAGCT[C/T]CAAGTAATTGGTCTC | 57799 |
| rs573473604 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:590509 | GGAGCTCGCCCTCGG[C/T]CCGGCCCTTCCAAGC | 57799 |
| rs573604388 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:623595 | GAAGCGGAGATCGTG[C/T]GGCTGCACTCCAGCC | 57799 |
| rs573605157 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:620792 | CCGCGGGCATCCCAG[A/C]CCCCCGCCGACGGGC | 57799 |
| rs573614605 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589182 | CGGCCGCGTCCCCGG[C/G]CGGAAGGCTCACGCT | 57799 |
| rs573678983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589824 | GTGGGAAAGGCGGGG[A/G]AGGGGCGGTCATGAC | 57799 |
| rs573697923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629616 | GGTCCTCCAGTCAGT[C/T]GGCCCGCTCAGCAGA | 57799 |
| rs573833933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:605137 | GGCTGAGGCAGGAGG[A/G]TCGTGTGAGCCCTGG | 57799 |
| rs573964848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:599539 | GTGAAAATGCACACC[C/T]GTGGGTGTTCGCTAC | 57799 |
| rs573976245 | snp | A/C | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588527 | GGGAGACCCTGTTTC[A/C]AAAAAGAAAAAACTG | 57799 |
| rs574052784 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | RAB40C | GRCh38.p7 | 16:600024 | AGTCAGCGTGGATTC[A/G]CAAGGTTTTGTTCCC | 57799 |
| rs574115054 | snp | C/T | 0.00129786 | 0.025441 | intron-variant | RAB40C | GRCh38.p7 | 16:625051 | GCTCTGTCCCAGGTA[C/T]TCCCGGGGGGATTCA | 57799 |
| rs574175417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:625581 | GGCCCCGGGTAGGCT[C/T]TGGATTCCCGCCTGC | 57799 |
| rs574178241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595813 | TCACTGTGTTGGCCA[A/G]GCTGGTCTTGAACTG | 57799 |
| rs574188996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595267 | GTGTAGCCCCCACCA[C/T]CACCTGTGAGAAGGC | 57799 |
| rs574189421 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:600524 | TTGGGAGGCCGAGGC[A/G]GGCGGATCACAAGGT | 57799 |
| rs574321250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:621540 | CGCGGCTCTTCCCGC[A/G]AGGCCCTTCACGTGC | 57799 |
| rs574339075 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:599331 | TGCCCGTGTCGGCCG[G/T]CCACAGCCCTAGTGG | 57799 |
| rs574368769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:611069 | TGACGCGCACCGTGG[A/G]CAACCGGGTGCGGAG | 57799 |
| rs574370771 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:616796 | AAAGGCACTGCCCTT[G/T]CTCCAGGCACGCTGG | 57799 |
| rs574411260 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:600776 | AAAATAAGAGCTTTG[C/G]TGCCTACGTGCGTCA | 57799 |
| rs574414996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:626973 | GCGAGTGCTCTAGGG[A/G]ATGAGTCAGGACGCG | 57799 |
| rs574432357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:616486 | TGGGATTAAAGGTGC[C/T]CACCACCACACCTGG | 57799 |
| rs574447398 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:592579 | CTGCCCCAGAATTGG[A/T]AACTCCTGACTCAGG | 57799 |
| rs574458827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:602074 | GAGGTTGCAGTGAGC[C/T]GAGATTGCACCACTG | 57799 |
| rs574551245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622601 | CAACCTCCGCCTCCC[A/G]GGTTCACGCCATTCT | 57799 |
| rs574567289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622815 | GGCCGAAGTCGCTAG[C/T]TTTTTAAAAATCAGA | 57799 |
| rs574577493 | snp | C/T | 8.25035e-05 | 0.00642222 | synonymous-codon | RAB40C | GRCh38.p7 | 16:627472 | GGCCAACGGCATGAA[C/T]GCGGTCATGATGCAC | 57799 |
| rs574581370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:598018 | TTGGGAGGCCAAGGT[A/G]GGTGAATCACGAGGT | 57799 |
| rs574698206 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RAB40C | GRCh38.p7 | 16:607778 | CCTGGGCGACAGAGC[A/G]AGACTCCGTCTCAAA | 57799 |
| rs574700626 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587866 | AGGCTGGAGTGCAGT[C/G]GCACAATCTCAGCTC | 57799 |
| rs574721567 | in-del | -/GTG | 0.14665 | 0.227637 | intron-variant | RAB40C | GRCh38.p7 | 16:618907 | AGTGTGTGCTCAGGT[-/GTG]GTGTACTTGGAGCTG | 57799 |
| rs574801294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:599008 | GGTCAGCAACGTTGT[C/T]GGCCACCTGGGCACA | 57799 |
| rs574837269 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:604399 | GAATCCTTCTGAAGG[G/T]GTTTCTCTAGAATAC | 57799 |
| rs574840874 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | RAB40C | GRCh38.p7 | 16:614311 | ACTGCTAACTCTGCC[A/G]CATCCCGATGGTGAA | 57799 |
| rs574904075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:618860 | GTGCAGGCATGTGCA[C/T]AGGTCTGGCGGGGGC | 57799 |
| rs575112127 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628483 | CTCGGCAGCTTCTGT[C/T]GCTGGCCCTGGGGTC | 57799 |
| rs575226520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:598042 | ACGAGGTCAAGAGAT[C/T]GAGACCATCCTGGCC | 57799 |
| rs575280423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622903 | TGAGACACGCAGCTG[A/G]GGGTGCTTAGGGTGC | 57799 |
| rs575309009 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:614917 | ACTGCCTAACTCTAC[C/T]GCATCCTGATGAACT | 57799 |
| rs575358642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:618901 | TGTGTGCAGTGTGTG[C/T]TCAGGTGTGTACTTG | 57799 |
| rs575363629 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587940 | AGCCTCCTAAGTAGC[A/T]GGGATTACAGGCACG | 57799 |
| rs575365472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593694 | CACCTGAGGCAGTGG[C/T]GTGTGACCACACGCC | 57799 |
| rs575461582 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594344 | GTTGTGGGGAGAAAC[A/G]GAGGGAGGCGGTTGT | 57799 |
| rs575495558 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:619424 | CGCTTGGCCACCCTC[A/G]TTTCTGTCTCCTCTG | 57799 |
| rs575545651 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant | RAB40C | GRCh38.p7 | 16:620942 | TGAGAACTAAAAAAG[-/A]AAAAAGCAGTTCATA | 57799 |
| rs575548059 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594612 | CTTGAGAGGCTCCTC[C/G]GTGTTTCATTGTCCT | 57799 |
| rs575591987 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RAB40C | GRCh38.p7 | 16:614679 | ACTTTACCTCGTCCC[A/G]ATGGTGAACTGCCTA | 57799 |
| rs575593875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:608252 | AAAACCATCAGGTGT[C/T]GGGAGAACTCACTCA | 57799 |
| rs575601211 | in-del | -/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:602437 | TTTTTTAATAAATTA[-/T]TTTTTTATTTTTGAG | 57799 |
| rs575655253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:614373 | TGCCAAACTTTACCT[C/T]GTCCCGATGGTGAAC | 57799 |
| rs575685057 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:599143 | TTGCCGAGGTGCTGT[A/G]TTTCGGTCCAGAAAG | 57799 |
| rs575872436 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | RAB40C | GRCh38.p7 | 16:621453 | GTCCCCGCGGCCTGG[G/T]TCTTGCAGATGGCAC | 57799 |
| rs575905196 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628959 | ACTCGCCCCATGGCC[C/T]GTTCCTGGGAGATGA | 57799 |
| rs575918124 | snp | C/T | 0.00517822 | 0.0506191 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628550 | TCAGAACCATCCTGA[C/T]CTTCTTAGGGACGTG | 57799 |
| rs575939476 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:591471 | GATGACAGGTCCTTA[A/T]AGGCACGCTGTTCCC | 57799 |
| rs575941578 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:611198 | GTGGGTGACGTGGTC[C/T]CCAGGCTTTTCCCGG | 57799 |
| rs575942110 | snp | A/G | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628065 | CGAGAGGGGACTCGC[A/G]GCCGCGATGGCAAGG | 57799 |
| rs575984568 | snp | A/G | 6.61507e-05 | 0.00575074 | intron-variant | RAB40C | GRCh38.p7 | 16:617318 | GAGGACACAAATGCC[A/G]AAGGGAGAACAGAAC | 57799 |
| rs576038417 | snp | C/T | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596980 | TTTCTGGACGTTTGT[C/T]CTTCAGAAATTAGCG | 57799 |
| rs576040048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:624180 | ACTTCTGAGTTGTGG[A/G]CTTGCCATGCGGGAG | 57799 |
| rs576062914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:592298 | TCCCCCACTCTCTCA[A/G]CTCGGGGGTTGGCAG | 57799 |
| rs576068327 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:606703 | CGGCTTCTCCAGGCC[A/G]CCTGCGTTGTTCACG | 57799 |
| rs576077038 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:611405 | GCCTTTGTGGCAATC[A/G]TGGTGTCCAACTTTG | 57799 |
| rs576112594 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RAB40C | GRCh38.p7 | 16:613435 | CCGCCCTGGCCGGTA[C/G]AATCAAGAGCACAGT | 57799 |
| rs576155605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:601511 | GGCAGGTCCCCGCCG[C/T]AGCCGCGTCAGCAGA | 57799 |
| rs576201438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:607313 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCATC | 57799 |
| rs576229926 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:626253 | CGCGCAGTAGGGGCT[C/T]GGCCGGCGGCAGGTC | 57799 |
| rs576335527 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:607740 | AGCTTGCAGTGAGCC[C/G]AGATCGCGCCACTGC | 57799 |
| rs576343139 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622521 | CGTTCTTTTGTTTTG[G/T]TTTTTGAGACACGGT | 57799 |
| rs576378764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:622310 | TCACGAGCAGGCGGG[A/G]GTGCTGGGCCTGAGC | 57799 |
| rs576442559 | snp | C/T | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:626355 | CCCTCAGGGTGCCGC[C/T]GTGGCCGCTGCACTC | 57799 |
| rs576476291 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588058 | CACCCACCTCAGCCT[C/T]CCAAAGTGCTGGGAT | 57799 |
| rs576525761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:617622 | CCGAGGCAGGAGGAT[C/T]ACCTGAGGTCAGGAG | 57799 |
| rs576528755 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:626899 | GCGGAGATCGTGCCA[C/T]GGCACTCCAGCCTGG | 57799 |
| rs576669379 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RAB40C | GRCh38.p7 | 16:602195 | TTGATATCTTAAGTA[C/T]GTAAAATAATTGTGG | 57799 |
| rs576677227 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587420 | CCCTCCCTTCACTGG[A/G]CCTGCTGCCCCAGAG | 57799 |
| rs576757167 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:618685 | TACTTGGAGCTGTGT[A/G]TGTGCACAGGTGTAG | 57799 |
| rs576805389 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:620393 | TGAAACTCCATCTCA[A/G]AAAAAAAGGAGGAGC | 57799 |
| rs576846115 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RAB40C | GRCh38.p7 | 16:616474 | CTCCCGAGTAGCTGG[A/G]ATTAAAGGTGCCCAC | 57799 |
| rs576855108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596900 | CCTGGGGATGGCGGC[A/G]CACTCTGATACAGGC | 57799 |
| rs576864348 | in-del | -/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:614207 | CCCTATGGTGAACTG[-/C]CTAACTCTGCCGCAT | 57799 |
| rs576913469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:607746 | CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA | 57799 |
| rs577003051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:601995 | GCGGGGTGTGGTGTC[A/G]GGCACCTGTAATCCC | 57799 |
| rs577015325 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:601531 | GCGTCAGCAGAGCAA[C/T]GTGATCGTTGCTGGG | 57799 |
| rs577031068 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:599063 | CTAGCTGGGAGGGGC[A/G]GTAATAGGGTAGATG | 57799 |
| rs577081754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:592507 | CCACTGGGGCATTGG[A/G]GGCTCACACGTTAGG | 57799 |
| rs577102137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:626923 | AGCCTGGCGACAGAG[C/T]GAGACCCGTCTCAAA | 57799 |
| rs577115817 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:626419 | TGGGCAGTGTGTGCT[C/T]GCTCCTTCCTGGTTC | 57799 |
| rs577115991 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:613553 | GCTGGATCGTGGTGC[A/G]GTGGTGGCTTGGATG | 57799 |
| rs577182263 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:617688 | TCTCTACTAAAAATA[C/G]AAAAATTAGCCAGGT | 57799 |
| rs577274355 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:622568 | GCTGGAGTGCCGTGG[A/C]GCGATCTCGGCTCAC | 57799 |
| rs577303968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:610020 | GGGTGGGGATGTGAA[C/T]GGCACCAGCCTGGTG | 57799 |
| rs577364753 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RAB40C | GRCh38.p7 | 16:623596 | AAGCGGAGATCGTGC[A/G]GCTGCACTCCAGCCT | 57799 |
| rs577469247 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:598057 | TGAGACCATCCTGGC[C/T]AACATGATGAAACCC | 57799 |
| rs577523216 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:591811 | CATGTCGGCCAGGAT[A/G]GTCTCAATCTCCTGA | 57799 |
| rs577525582 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40C | GRCh38.p7 | 16:605542 | CTAGTTTTCACGTCA[A/G]TGGAGCCACACAGGG | 57799 |
| rs577611723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:625597 | TGGATTCCCGCCTGC[C/T]GCCCCTCCTGTGGCC | 57799 |
| rs577713924 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:615936 | CACTGCACTGCAGCC[G/T]GGGCGACAGAGTGAG | 57799 |
| rs577722809 | snp | C/T | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628952 | CCAGTGGACTCGCCC[C/T]ATGGCCCGTTCCTGG | 57799 |
| rs577732456 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:624801 | CTCTGAGTGTGAGCA[G/T]TGTGCTCCCCTGTGC | 57799 |
| rs577749780 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | RAB40C | GRCh38.p7 | 16:625970 | GCGGCAGGTCCCGAC[A/G]GAGCAGGCCCGCGCG | 57799 |
| rs577760396 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RAB40C | GRCh38.p7 | 16:591646 | CGCCAGGCTGGAGTG[C/T]AGTGGCACAATTTCA | 57799 |
| rs577829353 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:614763 | AACTGCTAACTCTGC[C/T]GCATCCCGACGGTGA | 57799 |
| rs577838486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:621588 | CCTAGACTTCATGGT[C/T]GTGTTTGCATATTCT | 57799 |
| rs577851836 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RAB40C | GRCh38.p7 | 16:600568 | CCGTTCTGACCAACA[C/T]GGTGAAACCCCGTCT | 57799 |
| rs577982248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595918 | TAATTGTGCTGTTTT[A/G]TAAGTTGGACTGGCA | 57799 |
| rs578061115 | snp | C/T | 0.00261878 | 0.0360906 | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596284 | AGGGATCTGGGTCCT[C/T]GCAGGTACTTTTGCC | 57799 |
| rs578080716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:616876 | CCTTGCACCCAGCGC[A/G]GGCCACAGGCGGAGG | 57799 |
| rs578156774 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:590995 | CGGTAGAAGGCGTCA[A/T]GGGCCAAAAGGAAGG | 57799 |
| rs578184730 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:621869 | AGGGGGTTTATGTGG[A/C]GCGTGGTACGGGAGG | 57799 |
| rs578202840 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:617151 | GGCCGAGGCTGGTCT[C/T]GCGGGCGCTCGCTCC | 57799 |
| rs578246569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40C | GRCh38.p7 | 16:606116 | CACATAGTCCTCTCG[A/G]TCCTCAGTCCAGTGT | 57799 |
| rs745387115 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594520 | CTCCCTGAGCTTTCT[C/T]CAAACAGTTACAAAC | 57799 |
| rs745391273 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:604727 | AGCTTGCCCAGCCTG[C/G]GCAACATAGTGAGAA | 57799 |
| rs745451139 | snp | A/T | 1.76316e-05 | 0.00296909 | missense | RAB40C | GRCh38.p7 | 16:627605 | AACTGCTCGCGGAGT[A/T]ACTGCAAGATCTCCT | 57799 |
| rs745481163 | snp | C/T | | | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595695 | GCAAGCTCCACCTCC[C/T]GGGTTCAAGTGATTC | 57799 |
| rs745502443 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:618301 | TGCTTTTCAAAGGAT[A/G]TTTCTCCTGATTCTT | 57799 |
| rs745503618 | snp | C/T | 3.88357e-05 | 0.0044064 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627653 | CCGCCTGTGCAGATG[C/T]CAGGAGGGCTCGAGC | 57799 |
| rs745540719 | snp | C/T | 0.000185512 | 0.00962919 | intron-variant | RAB40C | GRCh38.p7 | 16:624995 | ACTGGCATTCTGCTC[C/T]GCAAGTTTTAGGTTG | 57799 |
| rs745588252 | snp | A/G | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628056 | GGGACTCCTCGAGAG[A/G]GGACTCGCGGCCGCG | 57799 |
| rs745673052 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:624458 | CTGTCGCTCCATCCT[C/G]AGCAAGGCCTTCGCC | 57799 |
| rs745772815 | snp | C/G | 4.38991e-05 | 0.00468483 | utr-variant-5-prime | RAB40C | GRCh38.p7 | 16:590283 | GCGCGGGGCGCAGGC[C/G]GCGCGGCCATGGGCT | 57799 |
| rs745774805 | snp | C/T | 1.66112e-05 | 0.00288189 | missense | RAB40C | GRCh38.p7 | 16:626085 | CGCATCGTGCTCATG[C/T]GGCACGGCATGGAGA | 57799 |
| rs745828292 | snp | C/G | 3.68331e-05 | 0.00429129 | synonymous-codon | RAB40C | GRCh38.p7 | 16:590402 | GAGCCTGCAGGACGG[C/G]GCGGCAGAGTCCCCG | 57799 |
| rs745894349 | in-del | -/A | 0.00276985 | 0.0371114 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629626 | TCAGTCGGCCCGCTC[-/A]GCAGAGCCGCCTGCA | 57799 |
| rs745918806 | in-del | -/TTCTGAGGGTGTTTCTCTAGAATACACGTGAGTCT | | | intron-variant | RAB40C | GRCh38.p7 | 16:604597 | AATACACGTGAGTCC[lengthTooLong]TTCTGAAGGTGTTTC | 57799 |
| rs746072644 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:603262 | CTAGAATTTCTTCTG[A/C]CATTTGGCATGCTGG | 57799 |
| rs746189447 | snp | A/C | 1.67702e-05 | 0.00289566 | intron-variant | RAB40C | GRCh38.p7 | 16:625408 | TGTCAGTGACCCCTG[A/C]TGACCCCCAAGTCTC | 57799 |
| rs746224969 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:622944 | GCGGCTGCTGGTCAC[C/T]GAGAGTCTCCTTTTG | 57799 |
| rs746248855 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:600317 | AGTATGTCAGCTTCT[G/T]AAATTACTTTATTAA | 57799 |
| rs746355354 | snp | C/G | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628875 | CGGGACCCAGGACCC[C/G]CCGTGGTGGACTCCG | 57799 |
| rs746491567 | in-del | -/T | | | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595603 | ATAACTTTTTTCTTC[-/T]TTTTTTTTTTTTTTT | 57799 |
| rs746511445 | snp | A/G | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627998 | TGGCCCGGTGGTGGT[A/G]CACTGGTGACTTCAT | 57799 |
| rs746623951 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:627314 | CTCCCCCACAGCCCC[A/G]TGGTCTGACACCCCC | 57799 |
| rs746643066 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593584 | GCCTGGAAGTCTTGT[C/T]TGGCATGTTCCTCAG | 57799 |
| rs746699434 | snp | A/G | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594354 | GAAACGGAGGGAGGC[A/G]GTTGTGGACATGGCG | 57799 |
| rs746920810 | snp | A/G | 1.71888e-05 | 0.00293157 | intron-variant | RAB40C | GRCh38.p7 | 16:625547 | CTCCCGGGGAAGGCA[A/G]GCTGGATGGAGGTAC | 57799 |
| rs746975761 | snp | A/G | 1.66921e-05 | 0.00288891 | missense | RAB40C | GRCh38.p7 | 16:625983 | ACGGAGCAGGCCCGC[A/G]CGTACGCAGAGAAGA | 57799 |
| rs747002631 | snp | C/T | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587968 | ACGTACCAACATGCC[C/T]GGCTCATTTTTGTAT | 57799 |
| rs747140539 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:602549 | GCCTCTTGCCTCAGC[C/T]CCCCGAGTAGCTGGG | 57799 |
| rs747285314 | snp | A/G | 0.000374602 | 0.0136807 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596332 | ATTGCAGCTGAGAAG[A/G]CGCGAAGCTGCTGGT | 57799 |
| rs747293285 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:625572 | AGGTACCTGGGCCCC[A/G]GGTAGGCTCTGGATT | 57799 |
| rs747299253 | snp | A/T | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596806 | GCCTCTTCAGTCCTC[A/T]TGGCAGTGAAGGTAA | 57799 |
| rs747315894 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:607652 | AAAAATTAGGCAGGC[A/G]CGGTGGTGGGCGCCT | 57799 |
| rs747330506 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:609175 | ATGGTTTGGGAACAG[C/T]GGTGCTGCCACGGCT | 57799 |
| rs747355526 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:608253 | AAACCATCAGGTGTC[A/G]GGAGAACTCACTCAC | 57799 |
| rs747357562 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:601437 | CGGGTCGCCAGGATC[C/T]GGCTCAGAGTGTGAG | 57799 |
| rs747422428 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:622651 | TAGCTAGAACTAGGT[C/G]TGCACCACCGCGTCC | 57799 |
| rs747437679 | snp | G/T | 1.67125e-05 | 0.00289067 | missense | RAB40C | GRCh38.p7 | 16:618211 | TCAGGGACACGTCGG[G/T]CCAGGGCCGGTTCTG | 57799 |
| rs747441319 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:622219 | TTTATCGTGTAGGTC[A/G]AGTTGATCAAAAAAA | 57799 |
| rs747564404 | snp | C/T | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596915 | GCACTCTGATACAGG[C/T]AGTGCGCGGCTGTCT | 57799 |
| rs747611805 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:621344 | AGGGTTTCTCCCGCC[A/G]CCCCTGATGAGACAC | 57799 |
| rs747666714 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:625861 | GAGGGGTGGGTGGCA[A/C]CCTGCGTTTGTGCGT | 57799 |
| rs747777372 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:608179 | TCATGGCGGAAGGTA[C/G]CTCACACAGGGCAGC | 57799 |
| rs747822516 | snp | C/G | 0.000202204 | 0.0100529 | utr-variant-5-prime | RAB40C | GRCh38.p7 | 16:590272 | GCAGGCGGCCGGCGC[C/G]GGGCGCAGGCGGCGC | 57799 |
| rs747841612 | snp | C/T | 1.65941e-05 | 0.00288041 | intron-variant | RAB40C | GRCh38.p7 | 16:617190 | CGCGTCCCCTCAGCG[C/T]CCTGTGCTTCCTCGC | 57799 |
| rs747853435 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:610940 | GGGAACAAGACACTC[A/G]GCTGACTGTGCTTAG | 57799 |
| rs747862382 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:592627 | GATTGTGAAGGTGGC[A/G]TTGCCTTCTAAAGCT | 57799 |
| rs747898366 | in-del | -/TTAA | | | intron-variant | RAB40C | GRCh38.p7 | 16:605343 | TCAGCTTTCCGTCTT[-/TTAA]TTAATCAGCTTTATT | 57799 |
| rs747917270 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:617850 | TCCGTCTCAAAAAAG[A/G]AAAAAAAAAAAGCAT | 57799 |
| rs747979004 | snp | C/G | 0.000164002 | 0.00905395 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629678 | CTATGCCCGGCCCAG[C/G]GGGGTGTGGACGCCC | 57799 |
| rs748000121 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:603460 | GCCCCGCACGTGAAT[G/T]ACTTAGAGCCCCAGG | 57799 |
| rs748003432 | snp | A/G | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596598 | CCACTGTGAGAAGGC[A/G]GGGAGACTGCTTGTC | 57799 |
| rs748038180 | snp | A/G | 1.66468e-05 | 0.00288498 | missense | RAB40C | GRCh38.p7 | 16:625463 | ATGACATCACCAACC[A/G]CTGGTCCTTTGACGG | 57799 |
| rs748085651 | in-del | -/C | 1.71811e-05 | 0.00293091 | intron-variant | RAB40C | GRCh38.p7 | 16:626154 | GGCCAGCCCTGAGGT[-/C]CCCGAACCTGGGCTG | 57799 |
| rs748090502 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:617059 | CCAGAGCCCCGAGAT[C/T]TCCCCCTGCCCCACT | 57799 |
| rs748092726 | in-del | -/GG | | | intron-variant | RAB40C | GRCh38.p7 | 16:590804 | TGGGGAAGGTGTCAT[-/GG]GTCTAGGATCATCTG | 57799 |
| rs748287497 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:610469 | TCAGTGGGCCTGCAC[A/G]GAGCAGCTGACCTTC | 57799 |
| rs748372419 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:624227 | TTGCCACTAGGGAGA[C/G]TGGGCTGTGTTGTAC | 57799 |
| rs748377538 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:623778 | ATAGCAAGATCCCAT[C/G]TCTAAAAAATGTTTA | 57799 |
| rs748403129 | snp | A/G | 1.66471e-05 | 0.00288501 | missense | RAB40C | GRCh38.p7 | 16:626101 | GGCACGGCATGGAGA[A/G]GATCTGGAGGCCCAA | 57799 |
| rs748465862 | in-del | -/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:591544 | AGAAGAAAATACCTC[-/T]TGTAATGAGTTACTG | 57799 |
| rs748526098 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:621229 | GACTGAGCATTTGGG[C/T]CACCCCGGGAGCCCA | 57799 |
| rs748641869 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:600620 | GCTTGGCCTGGTGGC[A/G]TGCACCTGTATTCCC | 57799 |
| rs748651730 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:602403 | AAGACCATAGGCATG[C/T]ACCACAACACCTGGC | 57799 |
| rs748696693 | snp | C/T | 3.40044e-05 | 0.00412323 | intron-variant | RAB40C | GRCh38.p7 | 16:618190 | CCCCTCCCCTCCCCG[C/T]ATGTTTCAGGGACAC | 57799 |
| rs748838437 | snp | C/G | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596793 | GGGTGGAAGAGGGGC[C/G]TCTTCAGTCCTCTTG | 57799 |
| rs748842232 | snp | A/G | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596467 | CGATGCCACCCCACC[A/G]AGGGCCGTTCTGGGG | 57799 |
| rs748910577 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:621142 | CACATGTTGGTCCTG[A/G]GTTGAGGGTGCCAGG | 57799 |
| rs748914540 | snp | A/G | 1.6708e-05 | 0.00289028 | intron-variant | RAB40C | GRCh38.p7 | 16:625425 | GACCCCCAAGTCTCT[A/G]TTGCAGGGGATCCTC | 57799 |
| rs748942840 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:605481 | CTGCAGGCCTCTCAC[A/G]CTCTGCCCCCGGCCT | 57799 |
| rs748978301 | snp | A/G | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628128 | GGCTGCCCAGAGGCC[A/G]GGGGAGCAGACAGGG | 57799 |
| rs749000286 | snp | A/G | 0.000164029 | 0.00905469 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629718 | CAGCTGAGCTGGAAC[A/G]GGGCACTCCAGTTGG | 57799 |
| rs749093677 | snp | C/T | 1.74931e-05 | 0.0029574 | intron-variant | RAB40C | GRCh38.p7 | 16:626172 | CGAACCTGGGCTGCC[C/T]TGATCACATGGAGGC | 57799 |
| rs749130086 | in-del | -/TT | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587804 | TTATTTTTGAGGCAC[-/TT]TTTTTTTTTTTTTTT | 57799 |
| rs749148876 | snp | A/G | 7.63621e-05 | 0.00617861 | intron-variant | RAB40C | GRCh38.p7 | 16:590480 | GCGGGGCCCGAGCCC[A/G]GCGAGCTGGGCACGG | 57799 |
| rs749162107 | snp | C/T | 1.87771e-05 | 0.00306401 | missense | RAB40C | GRCh38.p7 | 16:590407 | TGCAGGACGGCGCGG[C/T]AGAGTCCCCGTACGC | 57799 |
| rs749248220 | snp | A/G | | | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595933 | ATAAGTTGGACTGGC[A/G]TGGCCTTACTTAAAT | 57799 |
| rs749319139 | snp | A/T | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627759 | GGCTTTCCTCACACC[A/T]GAGCCGGGTGCGAGG | 57799 |
| rs749383875 | snp | A/G | 1.6531e-05 | 0.00287493 | intron-variant | RAB40C | GRCh38.p7 | 16:617300 | GCACTTCAGTTCCTG[A/G]GTGAGGACACAAATG | 57799 |
| rs749396825 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:609554 | CTTGAGGGTCACCAG[A/G]ATGTGAGGAAAGACC | 57799 |
| rs749403817 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:623721 | GGAAGTTGAGGCAGG[A/C]GGATCACTTGAGGCC | 57799 |
| rs749435431 | snp | A/G | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588139 | TTCTCAGGAAAGGAG[A/G]AGACGGCTGCTCACC | 57799 |
| rs749581889 | snp | A/G | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589107 | GCCGCTGCCGCAGTG[A/G]GCACGTCGGGCCGGG | 57799 |
| rs749614964 | in-del | -/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:601846 | AAAAAAAAAAAAAAA[-/G]GCCGGATGCGGTGGC | 57799 |
| rs749665013 | snp | A/G | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593229 | CCTCTTCATCAGGGT[A/G]AAGTTGGTGGATCTG | 57799 |
| rs749812962 | snp | C/T | 1.65825e-05 | 0.00287941 | synonymous-codon | RAB40C | GRCh38.p7 | 16:627523 | CAGCGGGGCCGGGGG[C/T]GGCGGCAGCAAGGGC | 57799 |
| rs749842877 | snp | C/T | 6.62131e-05 | 0.00575345 | synonymous-codon | RAB40C | GRCh38.p7 | 16:627376 | CTGCTGCCGGGCCAT[C/T]GTCTCCTGCACCCCC | 57799 |
| rs749872976 | in-del | -/A | 0.000185615 | 0.00963187 | intron-variant | RAB40C | GRCh38.p7 | 16:625021 | GGTTGGAAAACTCAG[-/A]AATGCCCCCACTCAG | 57799 |
| rs749880120 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:610274 | TGACCAGGACAGTGC[C/T]GTGTGTCTCATGGGG | 57799 |
| rs749892607 | snp | C/G | 3.88961e-05 | 0.00440982 | intron-variant | RAB40C | GRCh38.p7 | 16:590460 | CCCGCGGCGCGCGCT[C/G]CTACGCGGGGCCCGA | 57799 |
| rs749993084 | snp | A/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:601958 | TGGTGAAACTCCGTC[A/T]CTACTGAAAATATAA | 57799 |
| rs750090854 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:615051 | TGGAAACGAGGACCC[A/G]AGGGAGACCATCCGT | 57799 |
| rs750092819 | snp | A/G | 8.32244e-05 | 0.00645022 | intron-variant | RAB40C | GRCh38.p7 | 16:617178 | CTCCAGGAGTGGCGC[A/G]TCCCCTCAGCGCCCT | 57799 |
| rs750189034 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:608608 | GCCATGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 57799 |
| rs750195892 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:601073 | TCATTAGCGTTAAAG[C/T]TCTTCTCTCCTGATG | 57799 |
| rs750278730 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:607884 | CCTAGTAAAGCAAAC[A/G]CCTCAGTGACATTTT | 57799 |
| rs750308533 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:621778 | AGAATTTGGGGTCAG[C/T]GGGCTTAGTGCCAGG | 57799 |
| rs750317423 | snp | A/G | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588834 | GCTACTGAACGCAGA[A/G]CACGTATCACAAAGC | 57799 |
| rs750368726 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:606060 | TAATAAATACAGGGC[C/T]GCAATAGATGGCCTT | 57799 |
| rs750413803 | snp | C/T | 1.7251e-05 | 0.00293687 | intron-variant | RAB40C | GRCh38.p7 | 16:626157 | CAGCCCTGAGGTCCC[C/T]GAACCTGGGCTGCCC | 57799 |
| rs750446952 | snp | A/G | 0.000184485 | 0.00960252 | intron-variant, utr-variant-5-prime | RAB40C | GRCh38.p7 | 16:590249 | CGGCCTCACCCGGCG[A/G]TGCTTCGGCAGGCGG | 57799 |
| rs750504123 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:619575 | TGGGAGGGATTTGAG[C/T]GGGTCTGTCCTGTCT | 57799 |
| rs750504812 | snp | A/G | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594026 | CAGGGTGGTGGGCCC[A/G]TGTTGGCCCCCAGGA | 57799 |
| rs750577095 | in-del | -/C | | | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629314 | CTGGCAGTGGCGGTG[-/C]CCCCGTGCCAGGGGC | 57799 |
| rs750592828 | snp | C/G | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594992 | GCGTGGCTAATTTTT[C/G]TATTTTTAGTAGAGG | 57799 |
| rs750636999 | snp | C/T | 1.74894e-05 | 0.00295709 | synonymous-codon | RAB40C | GRCh38.p7 | 16:627580 | CCGTCCACCCCAGAG[C/T]CCCCCCCAGAACTGC | 57799 |
| rs750640197 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:617555 | TCACCTTAAAAAGCA[C/T]TTCCCAGCGGGGTGT | 57799 |
| rs750707413 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:607493 | GGACAACGAGAGTGA[A/C]ACTGTCTCAAAAAAA | 57799 |
| rs750725398 | snp | A/G | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627787 | AGGAGGAGCATGCAC[A/G]GACCAAGCGCGGCAG | 57799 |
| rs750810535 | snp | C/T | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587533 | CAGAGGGCACAGCAG[C/T]TTTCCAAGGATCTCA | 57799 |
| rs750860776 | snp | A/G/T | 6.77787e-05 | 0.00582112 | intron-variant | RAB40C | GRCh38.p7 | 16:625527 | AGGCCTGGGTCCGGG[A/G/T]AGCCCTCCCGGGGAA | 57799 |
| rs750940856 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:623515 | AAAAATTAGCCGGGC[A/G]TGGTGGCGGGCGCCT | 57799 |
| rs750960412 | snp | A/G | 2.53238e-05 | 0.00355827 | intron-variant | RAB40C | GRCh38.p7 | 16:625889 | CGTCTGCTGAGTTCT[A/G]TGCCCCCAGCATGCA | 57799 |
| rs750993639 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:625138 | CAGAACCCCGCATCT[A/G]CCTGCCCAGGAAACT | 57799 |
| rs751040600 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:602956 | GTAATCTGAGAGCTA[C/T]GGGATCTGCTCCTTA | 57799 |
| rs751043273 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:604977 | GCAGGACAATCACTT[C/G]AACCCGGGAGGCGGA | 57799 |
| rs751059991 | snp | A/C | 1.65839e-05 | 0.00287953 | synonymous-codon | RAB40C | GRCh38.p7 | 16:626066 | GTCCTTCACGGAGCT[A/C]TCCCGCATCGTGCTC | 57799 |
| rs751066951 | snp | C/T | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588724 | GGCTCTGCTCCTCGC[C/T]GGCGGGGCAGACGTG | 57799 |
| rs751155757 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:610032 | GAACGGCACCAGCCT[A/G]GTGGCTCGGGTGCCA | 57799 |
| rs751170210 | snp | C/G | 1.76761e-05 | 0.00297283 | missense | RAB40C | GRCh38.p7 | 16:590389 | GCGAGATCCTGGAGA[C/G]CCTGCAGGACGGCGC | 57799 |
| rs751256376 | snp | A/C | 5.09031e-05 | 0.0050447 | intron-variant | RAB40C | GRCh38.p7 | 16:626143 | GGGCGGGCGCCGGCC[A/C]GCCCTGAGGTCCCCG | 57799 |
| rs751277631 | snp | G/T | 3.17718e-05 | 0.00398558 | intron-variant | RAB40C | GRCh38.p7 | 16:590451 | AAGGCCCGGCCCGCG[G/T]CGCGCGCTGCTACGC | 57799 |
| rs751291711 | snp | C/G | 5.14708e-05 | 0.00507274 | intron-variant | RAB40C | GRCh38.p7 | 16:618183 | GTCCCGGCCCCTCCC[C/G]TCCCCGTATGTTTCA | 57799 |
| rs751461284 | snp | A/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:600278 | TCTGAAGAGCCTGTG[A/T]CCTCCTGGTGGGGAG | 57799 |
| rs751491865 | snp | A/G | 3.33645e-05 | 0.00408425 | intron-variant | RAB40C | GRCh38.p7 | 16:618275 | GGTAAGACCAGCACC[A/G]CTCTTTCCATTGCTT | 57799 |
| rs751532055 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:603183 | GAGCCCTTTTGGCTT[C/G]TTGTGGGTTTTAAGG | 57799 |
| rs751551123 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:600829 | TCATTATCAGCAAGC[A/G]GTGACTGCCCAGGTT | 57799 |
| rs751553522 | in-del | -/TTTGT | | | intron-variant | RAB40C | GRCh38.p7 | 16:621050 | ACAACTGGTTATGTC[-/TTTGT]TTTGTCTTGTTAACT | 57799 |
| rs751578828 | snp | C/T | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628813 | CCTCTACCTCCTGTC[C/T]TCAGGCCGTGCGGCA | 57799 |
| rs751593270 | snp | C/T | 3.37501e-05 | 0.00410779 | intron-variant | RAB40C | GRCh38.p7 | 16:625523 | AGGTAGGCCTGGGTC[C/T]GGGGAGCCCTCCCGG | 57799 |
| rs751666032 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:616676 | TTGGCCCTCCCTAAC[A/G]CCAACCTTGGCAGTT | 57799 |
| rs751694273 | snp | C/T | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627926 | CCTTTCTTATTTATA[C/T]AGAGAACACTTCACT | 57799 |
| rs751758057 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:626665 | AGCACGGGCCTGGCA[C/T]GGTGGCTCACTCCTG | 57799 |
| rs751758957 | snp | C/G | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593083 | GAGTCCTGTGGCCTC[C/G]AGCAGAGAAGGAAGC | 57799 |
| rs751811524 | snp | C/G | 3.30115e-05 | 0.00406259 | missense | RAB40C | GRCh38.p7 | 16:627403 | CCCCGTGCACCTCAT[C/G]GACAAGCTTCCACTG | 57799 |
| rs752117896 | snp | A/G | 0.000163921 | 0.00905172 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629720 | GCTGAGCTGGAACGG[A/G]GCACTCCAGTTGGTA | 57799 |
| rs752215122 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:622828 | AGTTTTTTAAAAATC[A/G]GATCAGTTTTAGAAA | 57799 |
| rs752233174 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:623416 | GCACTTTGGGAGGCC[A/G]AGGTGGGCAGATCGG | 57799 |
| rs752234919 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:609035 | TATGAGGAGCACGTG[A/C]GCCTAGGAGTTGGAG | 57799 |
| rs752242363 | snp | A/G | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587682 | TGTCCCAGGAGGTGG[A/G]AACTAGGCAGCAGTG | 57799 |
| rs752416579 | snp | C/T | 1.65778e-05 | 0.002879 | synonymous-codon | RAB40C | GRCh38.p7 | 16:626054 | CAACGTCATCGAGTC[C/T]TTCACGGAGCTATCC | 57799 |
| rs752433198 | snp | C/T | 1.65097e-05 | 0.00287308 | missense | RAB40C | GRCh38.p7 | 16:627491 | GTCATGATGCACGGC[C/T]GTTCCTACTCCCTGG | 57799 |
| rs752434975 | snp | C/T | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588524 | AAAGGGAGACCCTGT[C/T]TCAAAAAAGAAAAAA | 57799 |
| rs752627307 | snp | A/G | 1.65231e-05 | 0.00287424 | synonymous-codon | RAB40C | GRCh38.p7 | 16:617263 | GCGCGTGAAGCTGGA[A/G]CTCTGGTGAGTTGGG | 57799 |
| rs752684533 | snp | C/T | 0.000646418 | 0.0179664 | intron-variant | RAB40C | GRCh38.p7 | 16:618179 | CACAGTCCCGGCCCC[C/T]CCCCTCCCCGTATGT | 57799 |
| rs752685680 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593741 | CCCTGTGAGCTCTTC[C/T]GTGTCTCCTAATGTG | 57799 |
| rs752703249 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:626549 | TCCCGTGAAGCCCCC[C/G]TCAGGGAGGTGGTAC | 57799 |
| rs752739009 | snp | A/G | 1.68244e-05 | 0.00290033 | intron-variant | RAB40C | GRCh38.p7 | 16:625392 | CTGGGCTGGCCATGC[A/G]TGTCAGTGACCCCTG | 57799 |
| rs752766751 | snp | C/T | 1.67153e-05 | 0.00289091 | intron-variant | RAB40C | GRCh38.p7 | 16:618288 | CCGCTCTTTCCATTG[C/T]TTTTCAAAGGATGTT | 57799 |
| rs752775167 | snp | A/G | 0.000557155 | 0.0166813 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629531 | CTGTGCTGAGCCCTC[A/G]CTCACAGTCCCCGGC | 57799 |
| rs752792428 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:617939 | CTGGCAGGACAGTCT[C/T]CTGGAGCTCCCAGGC | 57799 |
| rs752953315 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:603939 | TCCCAAGTGGTATTC[C/G]TTTGCACAAATATAC | 57799 |
| rs752963341 | snp | A/G | 0.000315507 | 0.012556 | intron-variant | RAB40C | GRCh38.p7 | 16:625191 | GGAGGGAGGGGAAGC[A/G]GCATTTCTGACACCA | 57799 |
| rs752993353 | snp | C/T | 1.72496e-05 | 0.00293675 | synonymous-codon | RAB40C | GRCh38.p7 | 16:590363 | GGTGGGCGACAGCGA[C/T]GTGGGCAAGGGCGAG | 57799 |
| rs753018537 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:592202 | TGTTTCTTGGGCTCT[C/T]GTCCGTCCTGTCTGA | 57799 |
| rs753098727 | snp | A/G | | | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596176 | TCGTGTCGAGCACAC[A/G]TGTTGTGGCCTGCAC | 57799 |
| rs753111498 | snp | A/G | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595314 | TGCAGACGAGGGATT[A/G]AGGCTCAGGAGGCGG | 57799 |
| rs753123470 | snp | C/T | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628486 | GGCAGCTTCTGTCGC[C/T]GGCCCTGGGGTCCCC | 57799 |
| rs753261549 | snp | C/G | 1.90391e-05 | 0.00308532 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627635 | TAGCGGGGATGGGCG[C/G]GGCCGCCTGTGCAGA | 57799 |
| rs753298070 | in-del | -/GACC | | | intron-variant | RAB40C | GRCh38.p7 | 16:610851 | CCCTCTGAGAGTCCA[-/GACC]TTTTCCAGAGTGACA | 57799 |
| rs753325935 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:608072 | TCTCACGCTGCTAGG[A/G]AGAAATACCCCAGAC | 57799 |
| rs753373771 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:621912 | TGGCTTGTCGGCACA[C/T]AGGTGGGCGGGTGGA | 57799 |
| rs753400072 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:621468 | GTCTTGCAGATGGCA[C/G]CAGCAAAGGCCACCG | 57799 |
| rs753576096 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:599222 | CGGCCGAAGCTGCCA[C/G]TGACAGGAGACCCTT | 57799 |
| rs753579533 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:591119 | GGATCATCTGGGGTC[C/G]GAGGGAAGGTGTCAT | 57799 |
| rs753589868 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:626892 | GCAGTGAGCGGAGAT[C/G]GTGCCACGGCACTCC | 57799 |
| rs753741831 | snp | C/T | 3.30175e-05 | 0.00406296 | synonymous-codon | RAB40C | GRCh38.p7 | 16:627487 | CGCGGTCATGATGCA[C/T]GGCCGTTCCTACTCC | 57799 |
| rs753759258 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:592147 | TGCCATCTACGCTGG[C/T]GAACTTACCTCTCCT | 57799 |
| rs753777502 | snp | C/T | 1.65187e-05 | 0.00287386 | synonymous-codon | RAB40C | GRCh38.p7 | 16:627391 | CGTCTCCTGCACCCC[C/T]GTGCACCTCATCGAC | 57799 |
| rs753834083 | snp | C/G | 1.66067e-05 | 0.00288151 | intron-variant | RAB40C | GRCh38.p7 | 16:617187 | TGGCGCGTCCCCTCA[C/G]CGCCCTGTGCTTCCT | 57799 |
| rs753969216 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:616211 | CAGTGAGCAGAGATC[A/G]CACCACTGCACTCCA | 57799 |
| rs753991455 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:620296 | TACTTAGGAGGCTGA[A/G]GCAGGAGAATCGCTT | 57799 |
| rs754026121 | snp | C/G | 8.60326e-05 | 0.00655812 | missense | RAB40C | GRCh38.p7 | 16:627584 | CCACCCCAGAGCCCC[C/G]CCCAGAACTGCTCGC | 57799 |
| rs754110077 | snp | A/G | 1.89943e-05 | 0.00308168 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627630 | TCTCCTAGCGGGGAT[A/G]GGCGGGGCCGCCTGT | 57799 |
| rs754142791 | snp | G/T | 1.69223e-05 | 0.00290876 | synonymous-codon | RAB40C | GRCh38.p7 | 16:625958 | CCTGGCCTTCAAGCG[G/T]CAGGTCCCGACGGAG | 57799 |
| rs754197920 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:602040 | CTGAGGCAAGAGAAT[C/T]GCTTCAACCCAGGAG | 57799 |
| rs754268857 | in-del | -/AA | | | intron-variant | RAB40C | GRCh38.p7 | 16:613407 | CTCGCCTGTAGAATC[-/AA]GAGCAGGACTGCCGC | 57799 |
| rs754302418 | snp | A/C | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594165 | ACAAACCTTCCTGGG[A/C]GCAAGTTTTCCTCCC | 57799 |
| rs754308603 | in-del | -/CGGCGCGGGGCGCAGG | 0.000123948 | 0.00787137 | utr-variant-5-prime | RAB40C | GRCh38.p7 | 16:590265 | GCTTCGGCAGGCGGC[-/CGGCGCGGGGCGCAGG]CGGCGCGGGGCGCAG | 57799 |
| rs754370796 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:624128 | TGTGTCTGGCTTGTC[A/G]TTGTTATCAGCGCCA | 57799 |
| rs754442714 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:608083 | TAGGAAGAAATACCC[C/G]AGACTGGGTCATTTG | 57799 |
| rs754678917 | in-del | -/CTCT | | | intron-variant | RAB40C | GRCh38.p7 | 16:614545 | TGGTGAACTGCCTAA[-/CTCT]ACCTCGTCCCGATGG | 57799 |
| rs754700018 | in-del | -/TC | 8.36365e-05 | 0.00646616 | intron-variant | RAB40C | GRCh38.p7 | 16:625420 | CTGATGACCCCCAAG[-/TC]TCTGTTGCAGGGGAT | 57799 |
| rs754716343 | snp | C/G/T | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627840 | GGCTGCTGGTGCTTC[C/G/T]GGGAATCTTGGTCGG | 57799 |
| rs754791113 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:616873 | GTGCCTTGCACCCAG[A/C]GCGGGCCACAGGCGG | 57799 |
| rs754816141 | snp | A/G | 3.30306e-05 | 0.00406377 | missense | RAB40C | GRCh38.p7 | 16:627392 | GTCTCCTGCACCCCC[A/G]TGCACCTCATCGACA | 57799 |
| rs754851859 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:592148 | GCCATCTACGCTGGC[A/G]AACTTACCTCTCCTG | 57799 |
| rs754878942 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:626924 | GCCTGGCGACAGAGC[A/G]AGACCCGTCTCAAAA | 57799 |
| rs754957777 | snp | C/G | 1.65239e-05 | 0.00287431 | missense | RAB40C | GRCh38.p7 | 16:617252 | CTGGACGGCCGGCGC[C/G]TGAAGCTGGAGCTCT | 57799 |
| rs754992366 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:608785 | GGCAGAGGCACAAGA[A/G]TCACTTGAACCCAGA | 57799 |
| rs755045150 | in-del | -/TTTGT | | | intron-variant | RAB40C | GRCh38.p7 | 16:591564 | ATGAGTTACTGAACA[-/TTTGT]TTTGTTTTGTTTTCT | 57799 |
| rs755157251 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:601183 | GTGGAGCTGGTTTGA[C/G]TTTTAAAAAATTGTA | 57799 |
| rs755167831 | snp | C/T | 3.82636e-05 | 0.00437382 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627633 | CCTAGCGGGGATGGG[C/T]GGGGCCGCCTGTGCA | 57799 |
| rs755186586 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:605746 | ACTCTCACAGGGCTC[A/C]TGTGAGGAGTCTCAG | 57799 |
| rs755186676 | snp | A/G | 1.67036e-05 | 0.0028899 | intron-variant | RAB40C | GRCh38.p7 | 16:618284 | AGCACCGCTCTTTCC[A/G]TTGCTTTTCAAAGGA | 57799 |
| rs755203247 | in-del | -/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:624094 | TACTCAGCTGTCCCC[-/T]GAGGCTGGACATTTA | 57799 |
| rs755203829 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:605271 | ATTGTTTCATAGTCC[C/T]ATCAGCAATGCATGA | 57799 |
| rs755313770 | snp | A/G | 0.000163385 | 0.00903692 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629749 | TACAGGGACCAGACC[A/G]CAGCCTCTGGCTCAG | 57799 |
| rs755321969 | snp | G/T | 0.00173823 | 0.0294295 | missense | RAB40C | GRCh38.p7 | 16:625963 | CCTTCAAGCGGCAGG[G/T]CCCGACGGAGCAGGC | 57799 |
| rs755338874 | snp | A/G | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594186 | TTTTCCTCCCGCCAC[A/G]TTGGTCAGGGTGTGT | 57799 |
| rs755392094 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:615306 | CTGAAGAAGGGCACC[A/G]TAGGCAGAGAGACCG | 57799 |
| rs755572382 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:621102 | TCATTTTCCACATGC[A/G]AGGAGCAGGTTACAG | 57799 |
| rs755634782 | snp | C/G | 1.65364e-05 | 0.0028754 | synonymous-codon | RAB40C | GRCh38.p7 | 16:627379 | CTGCCGGGCCATCGT[C/G]TCCTGCACCCCCGTG | 57799 |
| rs755668269 | snp | A/T | 0.00023976 | 0.0109464 | intron-variant | RAB40C | GRCh38.p7 | 16:590463 | GCGGCGCGCGCTGCT[A/T]CGCGGGGCCCGAGCC | 57799 |
| rs755684311 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:601970 | GTCTCTACTGAAAAT[A/G]TAAAAGTTAGCGGGG | 57799 |
| rs755719835 | snp | C/T | 0.000326424 | 0.0127713 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629634 | CCCGCTCAGCAGAGC[C/T]GCCTGCACGCTGGCC | 57799 |
| rs755725416 | snp | C/T | 3.32519e-05 | 0.00407736 | intron-variant | RAB40C | GRCh38.p7 | 16:617182 | AGGAGTGGCGCGTCC[C/T]CTCAGCGCCCTGTGC | 57799 |
| rs755729904 | snp | A/G | | | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595792 | ATTTGTAGTAGAGAT[A/G]GGGTTTCACTGTGTT | 57799 |
| rs755839215 | in-del | -/TGTTTTTTTTTTTTTTGGTTT | | | intron-variant | RAB40C | GRCh38.p7 | 16:602246 | AGCAGTGGTCATCTC[-/TGTTTTTTTTTTTTTTGGTTT]TGTTTTTTTTTTTTT | 57799 |
| rs755934294 | snp | A/G | 1.65012e-05 | 0.00287234 | intron-variant | RAB40C | GRCh38.p7 | 16:626158 | AGCCCTGAGGTCCCC[A/G]AACCTGGGCTGCCCT | 57799 |
| rs756033863 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:607999 | GCAACGTGCTGTGCC[C/T]GTCCCCACCTCCCTC | 57799 |
| rs756050810 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:606606 | AGATGTTCTCTTGCT[C/T]GTTGGGAGGTTGGCA | 57799 |
| rs756062132 | in-del | -/CA | | | intron-variant | RAB40C | GRCh38.p7 | 16:600983 | GAAGGGGCCCTCTGG[-/CA]CCCCAGGAGCAGCCT | 57799 |
| rs756090083 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629190 | GCATCAACACTACCC[A/G]CGCTGCTGTTAGACA | 57799 |
| rs756120214 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:621781 | ATTTGGGGTCAGCGG[A/G]CTTAGTGCCAGGAAG | 57799 |
| rs756192543 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:605139 | CTGAGGCAGGAGGAT[C/T]GTGTGAGCCCTGGAG | 57799 |
| rs756253469 | snp | A/G | 1.65252e-05 | 0.00287443 | intron-variant | RAB40C | GRCh38.p7 | 16:617285 | TGAGTTGGGGCTGCG[A/G]CACTTCAGTTCCTGG | 57799 |
| rs756282714 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:604416 | TTTCTCTAGAATACA[C/G]GAGTCCTTCTGAAGG | 57799 |
| rs756326259 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:610143 | AGCGGCACCCTGTGC[A/G]GTAGACAGAACCAGC | 57799 |
| rs756385177 | in-del | -/C | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588162 | GCTCACCACTATCCA[-/C]CCCCCCGCTTCCAGG | 57799 |
| rs756438437 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:590812 | GTGTCATGGGTCTAG[A/G]ATCATCTGGGGTCCG | 57799 |
| rs756462614 | snp | G/T | 3.35362e-05 | 0.00409475 | intron-variant | RAB40C | GRCh38.p7 | 16:625409 | GTCAGTGACCCCTGA[G/T]GACCCCCAAGTCTCT | 57799 |
| rs756544904 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:611211 | TCCCCAGGCTTTTCC[C/T]GGCATCCCCGTTCCT | 57799 |
| rs756580963 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:623887 | CAGTGAGCCATGATC[A/G]TGCCACTGCATGAAC | 57799 |
| rs756588545 | snp | A/G | 0.000159401 | 0.00892608 | intron-variant, utr-variant-5-prime | RAB40C | GRCh38.p7 | 16:590257 | CCCGGCGGTGCTTCG[A/G]CAGGCGGCCGGCGCG | 57799 |
| rs756600870 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:602975 | ATCTGCTCCTTAAAA[C/G]ATGGGAGAGGAGAAT | 57799 |
| rs756605718 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593123 | CTGTGGAACGCGCTT[C/T]CTGTGTCTAAGGTCT | 57799 |
| rs756634744 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:624098 | CAGCTGTCCCCTGAG[G/T]CTGGACATTTAATTT | 57799 |
| rs756634811 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:610155 | TGCGGTAGACAGAAC[C/G]AGCAGCCGAGGCGCC | 57799 |
| rs756693334 | snp | C/G | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588736 | CGCCGGCGGGGCAGA[C/G]GTGACGGGCTCCGCA | 57799 |
| rs756704809 | snp | C/T | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628820 | CTCCTGTCCTCAGGC[C/T]GTGCGGCACGACATG | 57799 |
| rs756816738 | snp | C/T | 4.97822e-05 | 0.00498885 | synonymous-codon | RAB40C | GRCh38.p7 | 16:626075 | GGAGCTATCCCGCAT[C/T]GTGCTCATGCGGCAC | 57799 |
| rs756834600 | snp | A/G/T | 3.60368e-05 | 0.00424469 | synonymous-codon | RAB40C | GRCh38.p7 | 16:590393 | GATCCTGGAGAGCCT[A/G/T]CAGGACGGCGCGGCA | 57799 |
| rs756871791 | snp | A/C | 3.41542e-05 | 0.0041323 | intron-variant | RAB40C | GRCh38.p7 | 16:626146 | CGGGCGCCGGCCAGC[A/C]CTGAGGTCCCCGAAC | 57799 |
| rs756924745 | snp | A/G | 7.14158e-05 | 0.00597518 | intron-variant | RAB40C | GRCh38.p7 | 16:590457 | CGGCCCGCGGCGCGC[A/G]CTGCTACGCGGGGCC | 57799 |
| rs756925999 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:617004 | TGCCCCGCCCTGCCC[G/T]TGGCCCGTGTGCAGA | 57799 |
| rs757057993 | snp | C/T | 0.000451365 | 0.015016 | intron-variant | RAB40C | GRCh38.p7 | 16:618184 | TCCCGGCCCCTCCCC[C/T]CCCCGTATGTTTCAG | 57799 |
| rs757109995 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:619452 | CTGGGCCCCCAAGCA[C/T]GCTTTTGTGCTGACT | 57799 |
| rs757177417 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:601048 | GCCTCCTTGCAGAGC[C/T]ACCTCCTGGTCATTA | 57799 |
| rs757208414 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:620986 | CCAGGCTGAGGTCCT[A/G]GAAAGCAAGCTCTGT | 57799 |
| rs757210492 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:605361 | ATTAATCAGCTTTAT[C/T]GAGGTGTAATTTGTG | 57799 |
| rs757258143 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629436 | GGGTTCGCCTCAAAG[C/T]GAGGGCTGGAGCTGG | 57799 |
| rs757268637 | in-del | -/CTT | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587636 | GTGGGAGAAACCTGA[-/CTT]CTTCATCAGCCAGGG | 57799 |
| rs757307312 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:592536 | GGCCCCTGCACCTGC[C/T]GCCTCCTGGTCCTGC | 57799 |
| rs757358432 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:603217 | TAAGTAAAAGCTCTA[C/G]CTTCGCAGGAAACCA | 57799 |
| rs757405774 | snp | A/G | 1.65051e-05 | 0.00287267 | missense | RAB40C | GRCh38.p7 | 16:627404 | CCCGTGCACCTCATC[A/G]ACAAGCTTCCACTGC | 57799 |
| rs757459772 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:626808 | CCGGGCGTGGTGACG[C/T]ACACCTGTAGTCCCA | 57799 |
| rs757529766 | snp | A/G | 1.9245e-05 | 0.00310196 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627644 | TGGGCGGGGCCGCCT[A/G]TGCAGATGCCAGGAG | 57799 |
| rs757530655 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:609991 | TTTTAGGAAACAGAA[C/T]GGGTCCCACGGGAGG | 57799 |
| rs757696022 | snp | C/T | 0.000326264 | 0.0127682 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629608 | GAGGGCCAGGTCCTC[C/T]AGTCAGTCGGCCCGC | 57799 |
| rs757814916 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:604292 | ACACGTCATTTTAGC[C/T]ATATGTAGGGATACA | 57799 |
| rs757847726 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:599351 | AGCCCTAGTGGCTGC[C/T]CGCAGAGTCTTGCGC | 57799 |
| rs757957783 | snp | A/G | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587903 | ACCTCCGTTTCCCGA[A/G]TTTAAGCAATTCTTC | 57799 |
| rs757975981 | snp | C/G | 1.67581e-05 | 0.00289461 | missense | RAB40C | GRCh38.p7 | 16:625976 | GGTCCCGACGGAGCA[C/G]GCCCGCGCGTACGCA | 57799 |
| rs757996984 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:609146 | AACGTGGACTGATAG[A/G]TGAGAGAGGTTTGAT | 57799 |
| rs758104603 | in-del | -/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:625056 | GTCCCAGGTACTCCC[-/G]GGGGGATTCACTGAT | 57799 |
| rs758107101 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:622570 | TGGAGTGCCGTGGCG[C/T]GATCTCGGCTCACTG | 57799 |
| rs758111772 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:602838 | GCCTCCCAAAGTGTC[A/G]AGATGACAGGTGTTA | 57799 |
| rs758178772 | snp | A/G | 1.65356e-05 | 0.00287533 | missense | RAB40C | GRCh38.p7 | 16:627506 | CGTTCCTACTCCCTG[A/G]CCAGCGGGGCCGGGG | 57799 |
| rs758209162 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:604582 | GAAGGTGTTTCTCTA[C/G]AATACACGTGAGTCC | 57799 |
| rs758212953 | in-del | -/CTCTGTCTCAC | | | intron-variant | RAB40C | GRCh38.p7 | 16:598551 | GGTGACAGAGCGAGA[-/CTCTGTCTCAC]AAAAAAAAAAAAAAA | 57799 |
| rs758233916 | snp | C/T | 3.30508e-05 | 0.00406501 | intron-variant | RAB40C | GRCh38.p7 | 16:617275 | GGAGCTCTGGTGAGT[C/T]GGGGCTGCGGCACTT | 57799 |
| rs758311589 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:616589 | ATGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 57799 |
| rs758351486 | snp | A/G | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595543 | ATGACCCTGGCTGGC[A/G]TCTGAGAACCCATGT | 57799 |
| rs758355423 | snp | C/T | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628747 | TGCCTGCCCCAGCAG[C/T]CCCTCTGCACGGTCA | 57799 |
| rs758389558 | in-del | -/A | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593791 | GATCTCTAGGTCTGG[-/A]AAGGCTTTCCTTTCT | 57799 |
| rs758443759 | snp | A/G | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627896 | CTGGGCTTGACCGGC[A/G]GGGAGCCTGGTTGGC | 57799 |
| rs758500004 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:615352 | GGGCTGGGCCCGCAC[A/G]GAGAGACAGATGTGC | 57799 |
| rs758539744 | snp | A/G | 3.34582e-05 | 0.00408999 | intron-variant | RAB40C | GRCh38.p7 | 16:618296 | TCCATTGCTTTTCAA[A/G]GGATGTTTCTCCTGA | 57799 |
| rs758555396 | snp | C/G | 1.70081e-05 | 0.00291612 | intron-variant | RAB40C | GRCh38.p7 | 16:625532 | TGGGTCCGGGGAGCC[C/G]TCCCGGGGAAGGCAG | 57799 |
| rs758591668 | snp | G/T | 1.68545e-05 | 0.00290292 | intron-variant | RAB40C | GRCh38.p7 | 16:625381 | CGTCCCTGGGCCTGG[G/T]CTGGCCATGCGTGTC | 57799 |
| rs758593679 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:591419 | TGGTGGCAGGTGCTG[C/G]TGGGCTGCTCTTGGG | 57799 |
| rs758648551 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:624254 | GTACGCTTTGGTGGC[C/G]CACTCCCCAGTCTCT | 57799 |
| rs758789184 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:603070 | TCCTGCCTCAGCCTC[C/T]TGAGTAGCTGGGGCC | 57799 |
| rs758922769 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:615684 | GATGTGATGTGGGCC[A/G]GGCACGGTGGCTCAC | 57799 |
| rs758942656 | snp | A/T | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587711 | TGGCCCACGGCTGGG[A/T]CTGGAGAGCGTTTTA | 57799 |
| rs758992311 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:602505 | TGGCACGATCTTGGC[G/T]CACTGCAACGTCTGC | 57799 |
| rs759051226 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:592701 | CGTGTTTGTGCATGT[G/T]CAGAAGAGCACGGGA | 57799 |
| rs759205547 | snp | C/T | 1.66382e-05 | 0.00288424 | synonymous-codon | RAB40C | GRCh38.p7 | 16:618245 | CATCTTCAGGTCCTA[C/T]TCCAGGGGCGCTCAG | 57799 |
| rs759231630 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:603810 | CGGCTTCCATCACAT[A/G]GGCTGCTTTTTCCTG | 57799 |
| rs759297002 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:623437 | GGCAGATCGGGAGGT[C/T]AGGAGATCAAGACCA | 57799 |
| rs759319529 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:602987 | AAAGATGGGAGAGGA[A/G]AATTTTAAGAGATAG | 57799 |
| rs759353108 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:609854 | CTCAGGATGGAGGGC[A/G]GGAGCTGTGTGCCTG | 57799 |
| rs759427315 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:623957 | AAAGAAAATGCCATC[C/T]GCAGTGCTGGGACCT | 57799 |
| rs759429407 | snp | A/C/G | 4.95261e-05 | 0.00497604 | missense | RAB40C | GRCh38.p7 | 16:627488 | GCGGTCATGATGCAC[A/C/G]GCCGTTCCTACTCCC | 57799 |
| rs759469639 | snp | C/T | | | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596162 | TGGACACAGATGACT[C/T]GTGTCGAGCACACGT | 57799 |
| rs759484476 | snp | A/T | 1.67086e-05 | 0.00289033 | missense | RAB40C | GRCh38.p7 | 16:627549 | AGGGCAACAGCCTCA[A/T]GAGGTCCAAGTCCAT | 57799 |
| rs759521181 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:623387 | GGGCGCGGTGGCTCA[C/T]GCCTGTCATCCCAGC | 57799 |
| rs759542499 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:604132 | GATCTCAGCTCACTG[C/T]AGCCTCTACCTCTTG | 57799 |
| rs759615768 | snp | A/G | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593707 | GGCGTGTGACCACAC[A/G]CCCAGCACCTGTGGG | 57799 |
| rs759690479 | snp | G/T | 0.000642605 | 0.0179134 | intron-variant | RAB40C | GRCh38.p7 | 16:625161 | AGGAAACTTCCACAG[G/T]CTGATGGCTCCAGGG | 57799 |
| rs759766134 | snp | C/T | 0.000943841 | 0.0217032 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629473 | GCAGCTGGGCCTGGT[C/T]ACGGCCATTCTCCTC | 57799 |
| rs759820839 | snp | A/G | | | missense | RAB40C | GRCh38.p7 | 16:627492 | TCATGATGCACGGCC[A/G]TTCCTACTCCCTGGC | 57799 |
| rs759884295 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:620308 | TGAGGCAGGAGAATC[G/T]CTTGAACCCAGGAGG | 57799 |
| rs760011767 | snp | C/T | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627728 | GACTGTCCACACAGC[C/T]GCCTCAGAAGCGCCG | 57799 |
| rs760042619 | snp | A/G | 4.3757e-05 | 0.00467724 | missense | RAB40C | GRCh38.p7 | 16:590427 | TCCCCGTACGCCTAC[A/G]GTAACGGTAAGGCCC | 57799 |
| rs760124351 | snp | A/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:609517 | GAAGCCAGAGTCACC[A/T]GCTTCCTGGCTAGGG | 57799 |
| rs760163429 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:592055 | GGGCCTGGACCCAGC[C/T]GAATGGGATGTGGCC | 57799 |
| rs760247432 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:602768 | ATTGAGGTCTTGCCA[C/T]GTTGCCTAGGCTAGT | 57799 |
| rs760354318 | snp | A/G | 1.65255e-05 | 0.00287445 | missense | RAB40C | GRCh38.p7 | 16:617247 | TCCTGCTGGACGGCC[A/G]GCGCGTGAAGCTGGA | 57799 |
| rs760393740 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:608627 | GTAATCCCAGCACTT[C/T]AGGAGGCCGAGGCAG | 57799 |
| rs760456473 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:615065 | CGAGGGAGACCATCC[A/G]TCCATCCTAAAATTG | 57799 |
| rs760596169 | snp | A/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:603534 | GTTCAGGCTGTCTTG[A/T]AGGGTAATCCGGTCC | 57799 |
| rs760615654 | snp | C/G | 1.66799e-05 | 0.00288785 | missense | RAB40C | GRCh38.p7 | 16:625494 | CATCGACCGCTGGAT[C/G]AAGGAGATCGATGAG | 57799 |
| rs760677569 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:620274 | GGCGGGCGCTTATAA[C/T]CCCAGCTACTTAGGA | 57799 |
| rs760761770 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:603795 | CCAGCCCCCAGCAGT[A/C]GGCTTCCATCACATG | 57799 |
| rs760781885 | in-del | -/G | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594953 | GCCTCCTGAGTAGCT[-/G]GGATTACAGACGCCT | 57799 |
| rs760904407 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:619638 | AGAGCCCCTCCGGGG[C/T]CAGTTCGTGAGCCTG | 57799 |
| rs761034408 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:600731 | CACTCCAGCCTGGGC[A/G]ACAGAGTGAGACTCC | 57799 |
| rs761055535 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:590572 | GGCTTCCAGACTCGG[C/T]AGCTCGGTGGCTGCG | 57799 |
| rs761117112 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:624924 | TGGCAAAAAGTCCCC[A/G]TGGCAAAACCTGCTC | 57799 |
| rs761182946 | snp | C/T | 1.65864e-05 | 0.00287974 | missense | RAB40C | GRCh38.p7 | 16:626020 | TGACCTTCTTTGAGG[C/T]CAGCCCCCTGTGCAA | 57799 |
| rs761340708 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:590980 | AAGATGTCATGGTCC[C/G]GGTAGAAGGCGTCAT | 57799 |
| rs761375336 | in-del | -/GGCGCGG | 0.000189952 | 0.0097437 | utr-variant-5-prime | RAB40C | GRCh38.p7 | 16:590266 | CTTCGGCAGGCGGCC[-/GGCGCGG]GGCGCGGGGCGCAGG | 57799 |
| rs761430045 | snp | C/G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:592013 | ACAGAGTGAGTGAGA[C/G/T]GGTGTGGTCCTCATC | 57799 |
| rs761496827 | snp | A/G | 3.7048e-05 | 0.00430379 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627626 | AAGATCTCCTAGCGG[A/G]GATGGGCGGGGCCGC | 57799 |
| rs761513789 | snp | A/G | 3.31972e-05 | 0.004074 | missense | RAB40C | GRCh38.p7 | 16:627369 | AGGACCTCTGCTGCC[A/G]GGCCATCGTCTCCTG | 57799 |
| rs761549767 | snp | C/G | 1.66824e-05 | 0.00288806 | intron-variant | RAB40C | GRCh38.p7 | 16:618276 | GTAAGACCAGCACCG[C/G]TCTTTCCATTGCTTT | 57799 |
| rs761568805 | snp | A/G | 1.66679e-05 | 0.00288681 | intron-variant | RAB40C | GRCh38.p7 | 16:617176 | CGCTCCAGGAGTGGC[A/G]CGTCCCCTCAGCGCC | 57799 |
| rs761627768 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:602655 | CCAGGCTGGTCTCGA[A/G]TTCCTGACCTCAAGT | 57799 |
| rs761686867 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:622417 | GGACACGTCTGTAGA[C/T]GCTGAGGAAACTGAC | 57799 |
| rs761737432 | snp | C/G | 2.02284e-05 | 0.00318022 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627668 | CCAGGAGGGCTCGAG[C/G]TGGACACTCCTGGCT | 57799 |
| rs761820946 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:600749 | AGAGTGAGACTCCAT[C/G]TCAAAAAAATAAAAA | 57799 |
| rs761872325 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:601765 | CGATCCCCTGAGGCC[A/G]GGGGTTCAGACTAGG | 57799 |
| rs761887472 | snp | C/G | 1.66236e-05 | 0.00288297 | missense | RAB40C | GRCh38.p7 | 16:625997 | CGCGTACGCAGAGAA[C/G]AACTGCATGACCTTC | 57799 |
| rs761942566 | snp | A/C | 2.19392e-05 | 0.00331197 | synonymous-codon | RAB40C | GRCh38.p7 | 16:590306 | CATGGGCTCGCAGGG[A/C]AGTCCGGTGAAGAGC | 57799 |
| rs761989063 | snp | A/G | 0.000183998 | 0.00958985 | intron-variant | RAB40C | GRCh38.p7 | 16:625875 | ACCCTGCGTTTGTGC[A/G]TCTGCTGAGTTCTGT | 57799 |
| rs762075787 | snp | C/G | 0.000203066 | 0.0100743 | intron-variant, utr-variant-5-prime | RAB40C | GRCh38.p7 | 16:590244 | CGCCGCGGCCTCACC[C/G]GGCGGTGCTTCGGCA | 57799 |
| rs762079003 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593907 | TGGTGGCGAGTTACC[C/T]GGCAGGAATTATGCT | 57799 |
| rs762154057 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:609779 | CTCCCAGAAAATAGA[A/G]CAAAAAGAGATTAAA | 57799 |
| rs762156959 | snp | C/T | 0.000163948 | 0.00905246 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629727 | TGGAACGGGGCACTC[C/T]AGTTGGTACAGGGAC | 57799 |
| rs762208586 | snp | C/T | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597382 | AAACTGGGAAGGATT[C/T]GAATCCTGGATGGGT | 57799 |
| rs762271134 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:620236 | CATCTCTACGAAAAA[C/T]ACAAAAATTAGCCGA | 57799 |
| rs762271192 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:605036 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACTT | 57799 |
| rs762298490 | snp | A/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:599174 | TCACTGCTGCAGGGG[A/T]GGGGAGTATGGTCAC | 57799 |
| rs762331134 | snp | G/T | 1.65293e-05 | 0.00287479 | synonymous-codon | RAB40C | GRCh38.p7 | 16:617236 | GACCACCACCATCCT[G/T]CTGGACGGCCGGCGC | 57799 |
| rs762358947 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:619459 | CCCAAGCACGCTTTT[A/G]TGCTGACTGGATCTG | 57799 |
| rs762463524 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:623420 | TTTGGGAGGCCGAGG[C/T]GGGCAGATCGGGAGG | 57799 |
| rs762474491 | snp | C/G | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588198 | TCAGAAACCGAGGAG[C/G]AAACATCACATCTTT | 57799 |
| rs762524168 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:623993 | CTTACCTCACCTGGG[C/T]TGCACATCTCTCCTT | 57799 |
| rs762575664 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:604926 | TAGCCTGGTGTGGTG[C/G]TGGTGCTTGTGGTCC | 57799 |
| rs762736390 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:590781 | TCCTAGAGAAGGTGT[C/T]ATGGGCCTGGGGAAG | 57799 |
| rs762779175 | snp | A/G | 3.37872e-05 | 0.00411004 | missense | RAB40C | GRCh38.p7 | 16:627567 | GGTCCAAGTCCATCC[A/G]TCCACCCCAGAGCCC | 57799 |
| rs762832244 | snp | A/C | 3.45698e-05 | 0.00415737 | intron-variant | RAB40C | GRCh38.p7 | 16:618180 | ACAGTCCCGGCCCCT[A/C]CCCTCCCCGTATGTT | 57799 |
| rs762834719 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629347 | GTGCTGCTTCATACC[C/T]GGCAAACTGACCTCT | 57799 |
| rs762842184 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:613773 | GAGTCGTGGGCAACA[C/G]CCAGGTCTAGACCCA | 57799 |
| rs762932746 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:610900 | TGGTCAGAGGGCTCC[A/G]TGTGGTCAGTGGCTG | 57799 |
| rs762965438 | snp | C/T | 0.000478336 | 0.0154577 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627639 | GGGGATGGGCGGGGC[C/T]GCCTGTGCAGATGCC | 57799 |
| rs763012444 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:626609 | TTCACTGCTGAACAG[A/C]GAGAGGGTGGCTGAC | 57799 |
| rs763056441 | snp | A/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:598743 | GAGACCCTGTCTCAA[A/T]AAATAAAAAATAAAG | 57799 |
| rs763124385 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:600519 | GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC | 57799 |
| rs763157741 | snp | C/T | 0.000328246 | 0.0128068 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629717 | ACAGCTGAGCTGGAA[C/T]GGGGCACTCCAGTTG | 57799 |
| rs763220715 | snp | C/T | 1.67691e-05 | 0.00289556 | splice-donor-variant | RAB40C | GRCh38.p7 | 16:625511 | AGGAGATCGATGAGG[C/T]AGGCCTGGGTCCGGG | 57799 |
| rs763231823 | snp | C/T | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597348 | TCGCCGTCTTTACAG[C/T]GAACACAGTCCTCAA | 57799 |
| rs763233098 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:608475 | CAAACCTGGGAGGCC[C/T]AGGATGCTGGCTTCA | 57799 |
| rs763321397 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:607813 | AAAAGAAAAGAAAAG[A/G]AAGTCGCATCTGGTA | 57799 |
| rs763349730 | snp | C/T | 0.000350956 | 0.0132422 | intron-variant | RAB40C | GRCh38.p7 | 16:617164 | CTCGCGGGCGCTCGC[C/T]CCAGGAGTGGCGCGT | 57799 |
| rs763357767 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:609656 | ATGAAGAGCCAGACG[C/T]TGCCAGAGGGGAACG | 57799 |
| rs763386144 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:603981 | TATGCATTTACCTTG[C/T]TGATGCACATTTGGG | 57799 |
| rs763409393 | snp | A/G | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628266 | GAGGTGCACCTGGCA[A/G]CCCACATTTTTGTTG | 57799 |
| rs763445322 | snp | C/T | 2.79912e-05 | 0.00374097 | intron-variant | RAB40C | GRCh38.p7 | 16:590442 | AGTAACGGTAAGGCC[C/T]GGCCCGCGGCGCGCG | 57799 |
| rs763486815 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:611012 | CGTTGTTTCATAGTC[G/T]TCTTACACTTTTCCT | 57799 |
| rs763555849 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:611306 | GTCCCCGGGCCATCA[A/G]CATCTGTCTTGTGGG | 57799 |
| rs763723038 | snp | C/T | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588674 | CCCGGAGGCACAGCC[C/T]TGGTCGGGGCCCCTC | 57799 |
| rs763744120 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:590830 | CATCTGGGGTCCGAG[A/G]GAAGGTGTCATGGGC | 57799 |
| rs763820453 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:623429 | CCGAGGTGGGCAGAT[C/T]GGGAGGTCAGGAGAT | 57799 |
| rs763831476 | snp | A/G | 1.85882e-05 | 0.00304857 | synonymous-codon | RAB40C | GRCh38.p7 | 16:627622 | CTGCAAGATCTCCTA[A/G]CGGGGATGGGCGGGG | 57799 |
| rs763890795 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:604535 | GTGAGTCTTTCTGAA[A/G]GTGTTTCTCTAGAAT | 57799 |
| rs763900582 | snp | A/C | 1.69596e-05 | 0.00291196 | intron-variant | RAB40C | GRCh38.p7 | 16:626142 | TGGGCGGGCGCCGGC[A/C]AGCCCTGAGGTCCCC | 57799 |
| rs763909972 | snp | C/T | 1.71935e-05 | 0.00293197 | intron-variant | RAB40C | GRCh38.p7 | 16:618182 | AGTCCCGGCCCCTCC[C/T]CTCCCCGTATGTTTC | 57799 |
| rs763914513 | snp | A/G | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593891 | GAGTGCCCCTGGGTG[A/G]TGGTGGCGAGTTACC | 57799 |
| rs763930817 | snp | C/G | 3.48441e-05 | 0.00417383 | missense | RAB40C | GRCh38.p7 | 16:627579 | TCCGTCCACCCCAGA[C/G]CCCCCCCCAGAACTG | 57799 |
| rs764117321 | in-del | -/A | | | intron-variant | RAB40C | GRCh38.p7 | 16:617849 | TCCGTCTCAAAAAAG[-/A]AAAAAAAAAAAAGCA | 57799 |
| rs764129569 | snp | C/T | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628767 | CTGCACGGTCACCAT[C/T]GCCTGGGCCTGCCCA | 57799 |
| rs764130287 | snp | A/T | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597564 | TCTTGGCTCGCTGCA[A/T]CCTCTTGAGCCTCAT | 57799 |
| rs764216798 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:626624 | AGAGAGGGTGGCTGA[C/T]GGTGTCACTGTCCTT | 57799 |
| rs764248286 | snp | C/T | 5.05421e-05 | 0.00502678 | intron-variant | RAB40C | GRCh38.p7 | 16:625391 | CCTGGGCTGGCCATG[C/T]GTGTCAGTGACCCCT | 57799 |
| rs764259817 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:600555 | CAAGAGATCAAGACC[A/G]TTCTGACCAACATGG | 57799 |
| rs764303493 | snp | A/G | 1.68479e-05 | 0.00290236 | intron-variant | RAB40C | GRCh38.p7 | 16:625520 | ATGAGGTAGGCCTGG[A/G]TCCGGGGAGCCCTCC | 57799 |
| rs764437907 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:608607 | GGCCATGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 57799 |
| rs764439011 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:604016 | TTCCTGGTTTGGGGT[A/G]TTACGAATAATGCTG | 57799 |
| rs764469761 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:611332 | GTGGGTGTTGCTGGC[A/G]CCTGCCTGCTTGGCC | 57799 |
| rs764526048 | snp | A/G | 1.68145e-05 | 0.00289948 | synonymous-codon | RAB40C | GRCh38.p7 | 16:627352 | CACAGTGTTCAGCCT[A/G]CAGGACCTCTGCTGC | 57799 |
| rs764545001 | snp | C/T | 1.67089e-05 | 0.00289035 | intron-variant | RAB40C | GRCh38.p7 | 16:617166 | CGCGGGCGCTCGCTC[C/T]AGGAGTGGCGCGTCC | 57799 |
| rs764557861 | in-del | -/AAAG | | | intron-variant | RAB40C | GRCh38.p7 | 16:607846 | GCAGACAAAAAAGAA[-/AAAG]AAAAGAAAACGAAGT | 57799 |
| rs764605155 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:617468 | TGTCCCTAGAGATCG[C/T]GGCTCCCCTCCTGCC | 57799 |
| rs764616127 | snp | A/G | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597237 | GAGGGCTTGGTGCTG[A/G]GGGGCCTGGAGTTGT | 57799 |
| rs764701111 | snp | G/T | 0.000168364 | 0.00917354 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629553 | GTCCCCGGCAGCAGA[G/T]GGCCTGGGGCGGACT | 57799 |
| rs764707519 | in-del | -/GCAGGCGGCCGGCGCGGGGC | 0.000498215 | 0.0157753 | intron-variant, utr-variant-5-prime | RAB40C | GRCh38.p7 | 16:590256 | CCCGGCGGTGCTTCG[-/GCAGGCGGCCGGCGCGGGGC]GCAGGCGGCCGGCGC | 57799 |
| rs764743968 | in-del | -/C | 5.30181e-05 | 0.00514842 | intron-variant | RAB40C | GRCh38.p7 | 16:618169 | CACAGGGACCACAGT[-/C]CCCGGCCCCTCCCCT | 57799 |
| rs764812581 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:600744 | GCGACAGAGTGAGAC[G/T]CCATCTCAAAAAAAT | 57799 |
| rs764868604 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:599289 | CTGTGTCCTCAGGCT[C/T]TGCCAAGGCAGTGTC | 57799 |
| rs764930459 | in-del | -/CT | | | intron-variant | RAB40C | GRCh38.p7 | 16:624093 | TTACTCAGCTGTCCC[-/CT]GAGGCTGGACATTTA | 57799 |
| rs764958179 | snp | C/T | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587599 | ACAGGGCTGTGTCCA[C/T]AGGCTGTGGTGGGCA | 57799 |
| rs764987995 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:602514 | CTTGGCTCACTGCAA[C/T]GTCTGCCTCCTGGGT | 57799 |
| rs764988024 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:625066 | CTCCCGGGGGGATTC[A/C]CTGATGGACTGGCCG | 57799 |
| rs765010717 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:603844 | CAGACATCATGGATA[C/T]GAAGCAGACCCTGGT | 57799 |
| rs765088165 | snp | C/T | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628644 | AAAGGCCCACCAGCC[C/T]GGCGCTCATGCTGAG | 57799 |
| rs765090615 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:610679 | CGCCGTCCCCCAGCG[C/T]GGGCTCCAGGCCTCT | 57799 |
| rs765094110 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:592172 | TCTCCTGGTCCCTGC[C/T]CTCTCCCCTTGCTTT | 57799 |
| rs765125887 | in-del | -/A | | | intron-variant | RAB40C | GRCh38.p7 | 16:611799 | TGTAGAATCAAGAGC[-/A]AGGGACAGCCGCCTT | 57799 |
| rs765148251 | snp | A/G | 1.65233e-05 | 0.00287426 | synonymous-codon | RAB40C | GRCh38.p7 | 16:617257 | CGGCCGGCGCGTGAA[A/G]CTGGAGCTCTGGTGA | 57799 |
| rs765184054 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:592936 | CAGTATTGTGTAAGA[C/T]GTGGAGACCTGCCTG | 57799 |
| rs765219284 | snp | A/G | 1.67158e-05 | 0.00289096 | missense | RAB40C | GRCh38.p7 | 16:627551 | GGCAACAGCCTCAAG[A/G]GGTCCAAGTCCATCC | 57799 |
| rs765334532 | snp | C/T | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595423 | CCCCTGTCCTCCTCA[C/T]GTCCACCTGGGCCTG | 57799 |
| rs765351780 | snp | A/G | 7.61774e-05 | 0.00617113 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627634 | CTAGCGGGGATGGGC[A/G]GGGCCGCCTGTGCAG | 57799 |
| rs765498797 | snp | C/T | 1.65737e-05 | 0.00287864 | synonymous-codon | RAB40C | GRCh38.p7 | 16:626048 | CAACTTCAACGTCAT[C/T]GAGTCCTTCACGGAG | 57799 |
| rs765575068 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:621539 | CCGCGGCTCTTCCCG[C/T]GAGGCCCTTCACGTG | 57799 |
| rs765612758 | snp | A/G | 0.000254615 | 0.0112802 | intron-variant | RAB40C | GRCh38.p7 | 16:625180 | ATGGCTCCAGGGGAG[A/G]GAGGGGAAGCGGCAT | 57799 |
| rs765624453 | snp | C/G | 1.7254e-05 | 0.00293713 | missense | RAB40C | GRCh38.p7 | 16:590349 | CTCAAGTTCCTGCTG[C/G]TGGGCGACAGCGACG | 57799 |
| rs765666657 | snp | C/T | 1.69015e-05 | 0.00290696 | intron-variant | RAB40C | GRCh38.p7 | 16:626135 | AGGTGGGTGGGCGGG[C/T]GCCGGCCAGCCCTGA | 57799 |
| rs765674161 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:603036 | AGGCTGGTCTTGAAC[C/T]GTGGCGCTGAAGCAA | 57799 |
| rs765675659 | snp | C/T | 2.36936e-05 | 0.00344184 | synonymous-codon | RAB40C | GRCh38.p7 | 16:590432 | GTACGCCTACAGTAA[C/T]GGTAAGGCCCGGCCC | 57799 |
| rs765783814 | snp | C/T | 1.662e-05 | 0.00288266 | intron-variant | RAB40C | GRCh38.p7 | 16:617183 | GGAGTGGCGCGTCCC[C/T]TCAGCGCCCTGTGCT | 57799 |
| rs765789364 | snp | C/G | | | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596167 | ACAGATGACTCGTGT[C/G]GAGCACACGTGTTGT | 57799 |
| rs765889616 | snp | C/T | 1.65042e-05 | 0.0028726 | missense | RAB40C | GRCh38.p7 | 16:627480 | GCATGAACGCGGTCA[C/T]GATGCACGGCCGTTC | 57799 |
| rs765943081 | snp | C/T | 9.91408e-05 | 0.00703993 | missense | RAB40C | GRCh38.p7 | 16:617249 | CTGCTGGACGGCCGG[C/T]GCGTGAAGCTGGAGC | 57799 |
| rs765982971 | snp | A/G | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:589208 | ACGCTCGGTGACGCC[A/G]CGCTGTCCCAGAACC | 57799 |
| rs766063247 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:602781 | CATGTTGCCTAGGCT[A/G]GTGGTCTTGAACTCC | 57799 |
| rs766149225 | snp | G/T | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597621 | CCTCCTGAGTAGCTG[G/T]GATTACAGGCATGCA | 57799 |
| rs766241240 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:592136 | GCTTCAGGGAATGCC[A/G]TCTACGCTGGCGAAC | 57799 |
| rs766268780 | in-del | -/TTTTG | | | intron-variant | RAB40C | GRCh38.p7 | 16:622511 | AGCACTCGCTCGTTC[-/TTTTG]TTTTGTTTTTTGAGA | 57799 |
| rs766292623 | snp | C/T | 1.6519e-05 | 0.00287388 | missense | RAB40C | GRCh38.p7 | 16:627390 | TCGTCTCCTGCACCC[C/T]CGTGCACCTCATCGA | 57799 |
| rs766327971 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:623423 | GGGAGGCCGAGGTGG[A/G]CAGATCGGGAGGTCA | 57799 |
| rs766357084 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:622477 | GCAGGGCGAGCGCGC[A/G]TCCTGACTCATCCCC | 57799 |
| rs766378608 | snp | A/C | 1.71876e-05 | 0.00293147 | synonymous-codon | RAB40C | GRCh38.p7 | 16:627583 | TCCACCCCAGAGCCC[A/C]CCCCAGAACTGCTCG | 57799 |
| rs766505060 | snp | C/T | | | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596145 | TCTCTCGCAGGGTGG[C/T]GTGGACACAGATGAC | 57799 |
| rs766717152 | snp | A/G | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593128 | GAACGCGCTTTCTGT[A/G]TCTAAGGTCTCAAGG | 57799 |
| rs766733866 | snp | C/T | 1.70307e-05 | 0.00291806 | missense, intron-variant | RAB40C | GRCh38.p7 | 16:625939 | TGGTTGGAAACCGGC[C/T]GCACCTGGCCTTCAA | 57799 |
| rs766785912 | in-del | -/CTG | | | intron-variant | RAB40C | GRCh38.p7 | 16:614204 | CATCCCTATGGTGAA[-/CTG]CTGCTAACTCTGCCG | 57799 |
| rs766809807 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:625198 | GGGGAAGCGGCATTT[C/T]TGACACCATGGAAGG | 57799 |
| rs766820357 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:615084 | ATCCTAAAATTGGGA[A/C]GTTTGGTTTTCTGTT | 57799 |
| rs766897107 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629493 | CCATTCTCCTCTTCC[C/T]GGTGGATGGAATCCC | 57799 |
| rs766928136 | snp | A/C | 1.65765e-05 | 0.00287888 | missense | RAB40C | GRCh38.p7 | 16:626036 | CAGCCCCCTGTGCAA[A/C]TTCAACGTCATCGAG | 57799 |
| rs766979229 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:591039 | GGATCATCTGGGGTC[C/T]GAGGAAAGGTGTCAT | 57799 |
| rs767099159 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:607053 | GAGGGTCCCACTTCC[A/G]AGCCGAGGGTGCTAC | 57799 |
| rs767137288 | snp | A/G | 1.65886e-05 | 0.00287993 | synonymous-codon | RAB40C | GRCh38.p7 | 16:627370 | GGACCTCTGCTGCCG[A/G]GCCATCGTCTCCTGC | 57799 |
| rs767317724 | snp | C/G | 1.66969e-05 | 0.00288932 | intron-variant | RAB40C | GRCh38.p7 | 16:618278 | AAGACCAGCACCGCT[C/G]TTTCCATTGCTTTTC | 57799 |
| rs767396150 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:598664 | GGAAACTCACTGGAG[C/T]CTGGGAGGTGGTGGC | 57799 |
| rs767469226 | snp | A/G | 2.69545e-05 | 0.00367104 | intron-variant | RAB40C | GRCh38.p7 | 16:625884 | TTGTGCGTCTGCTGA[A/G]TTCTGTGCCCCCAGC | 57799 |
| rs767557244 | snp | G/T | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594022 | GGGCCAGGGTGGTGG[G/T]CCCGTGTTGGCCCCC | 57799 |
| rs767791986 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594973 | TACAGACGCCTGCCA[C/T]CATGCGTGGCTAATT | 57799 |
| rs767874488 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593061 | GCACACTTCCAGGTC[C/T]CCGCAGGAGTCCTGT | 57799 |
| rs767895737 | snp | G/T | 0.000163921 | 0.00905172 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629729 | GAACGGGGCACTCCA[G/T]TTGGTACAGGGACCA | 57799 |
| rs767959330 | snp | A/G | 1.65277e-05 | 0.00287464 | synonymous-codon | RAB40C | GRCh38.p7 | 16:617239 | CACCACCATCCTGCT[A/G]GACGGCCGGCGCGTG | 57799 |
| rs767976095 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:590582 | CTCGGTAGCTCGGTG[C/G]CTGCGGGGTGCCCGT | 57799 |
| rs768036676 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:605037 | CACTCCAGCCTGGGC[A/G]ACAGAGTGAGACTTT | 57799 |
| rs768051613 | snp | A/G | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587488 | CATCTGGGTTCCCTG[A/G]GACACTTTTCTGCTC | 57799 |
| rs768131555 | snp | C/G | 1.68986e-05 | 0.00290672 | intron-variant | RAB40C | GRCh38.p7 | 16:625525 | GTAGGCCTGGGTCCG[C/G]GGAGCCCTCCCGGGG | 57799 |
| rs768149237 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:603806 | CAGTCGGCTTCCATC[A/G]CATGGGCTGCTTTTT | 57799 |
| rs768332834 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:621207 | CAGGCGGGCCTCTGA[C/G]CGCCGTGACTGAGCA | 57799 |
| rs768354709 | in-del | -/AGG | | | cds-indel | RAB40C | GRCh38.p7 | 16:628249 | CAGGAGAGGGGAGAA[-/AGG]AGGTGCACCTGGCAG | 57799 |
| rs768414250 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:615757 | ACCTGAGGTCAGGAA[C/T]TTGTGACCAGCTTAG | 57799 |
| rs768502154 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:625686 | ACACGACAGTCGGGC[A/G]TGGAGCCCAGCAAGA | 57799 |
| rs768544602 | snp | C/T | 0.000187178 | 0.00967234 | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596281 | GGGAGGGATCTGGGT[C/T]CTCGCAGGTACTTTT | 57799 |
| rs768667205 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:613806 | TGGAATGCATGGTCT[C/T]GGGGCCTTGGTGGGG | 57799 |
| rs768686664 | in-del | -/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:598581 | AAAAAAAAAAAAAAA[-/G]AAAAAAGAAAATTAG | 57799 |
| rs768691724 | snp | C/T | 1.98348e-05 | 0.00314913 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627664 | GATGCCAGGAGGGCT[C/T]GAGCTGGACACTCCT | 57799 |
| rs768698408 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:623734 | GGAGGATCACTTGAG[G/T]CCAGGGGTTCAAGAC | 57799 |
| rs768773289 | snp | C/G | 1.65315e-05 | 0.00287498 | intron-variant | RAB40C | GRCh38.p7 | 16:617303 | CTTCAGTTCCTGGGT[C/G]AGGACACAAATGCCG | 57799 |
| rs768826083 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:623271 | AGCATCAAAAGTTAC[C/T]CCTCTCCAGCCTTTT | 57799 |
| rs768828703 | snp | A/T | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588159 | GGCTGCTCACCACTA[A/T]CCACCCCCCGCTTCC | 57799 |
| rs768877299 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:601910 | AGGTGGGTGGATCAC[A/G]AGGTCAGGAGATTGG | 57799 |
| rs768935791 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:609683 | AACGCTCAGAGCACC[A/G]GAAGGAGCTTTTAGA | 57799 |
| rs768949098 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:623161 | AGCACACTTGGAGCC[C/T]GAGGCAGCCCATCAG | 57799 |
| rs768989433 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:620209 | ACCAACCTGACCAAC[A/G]TGGTGAAACCCCATC | 57799 |
| rs769170804 | snp | C/T | 3.29951e-05 | 0.00406159 | synonymous-codon | RAB40C | GRCh38.p7 | 16:627448 | GAGCCACCTCAAGTC[C/T]TTCTCGATGGCCAAC | 57799 |
| rs769265595 | snp | C/T | 1.77432e-05 | 0.00297847 | synonymous-codon | RAB40C | GRCh38.p7 | 16:627610 | CTCGCGGAGTAACTG[C/T]AAGATCTCCTAGCGG | 57799 |
| rs769297585 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:598753 | CTCAAAAAATAAAAA[A/G]TAAAGAAAAGAGGAT | 57799 |
| rs769304242 | snp | G/T | 1.95609e-05 | 0.00312731 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627657 | CTGTGCAGATGCCAG[G/T]AGGGCTCGAGCTGGA | 57799 |
| rs769358797 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:618337 | ATGTGAGTTGTTGTC[C/T]TGTCAAACTCCCAAG | 57799 |
| rs769373957 | snp | A/G | 0.000185615 | 0.00963187 | intron-variant | RAB40C | GRCh38.p7 | 16:625022 | GTTGGAAAACTCAGA[A/G]ATGCCCCCACTCAGC | 57799 |
| rs769424091 | snp | C/G | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588083 | TGGGATTACAGGCAT[C/G]ACCCACCGTGCCCGG | 57799 |
| rs769510465 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:604817 | GTAGTCTCAGCACTT[G/T]GGGAGGCCGAGGCAG | 57799 |
| rs769670603 | in-del | -/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:623130 | CGGGAGGTGTGGCCA[-/G]GGCCCCCCGCGTCAC | 57799 |
| rs769744366 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:623958 | AAGAAAATGCCATCC[A/G]CAGTGCTGGGACCTG | 57799 |
| rs769763298 | snp | C/G | 0.000264176 | 0.0114899 | utr-variant-5-prime | RAB40C | GRCh38.p7 | 16:590287 | GGGGCGCAGGCGGCG[C/G]GGCCATGGGCTCGCA | 57799 |
| rs769795950 | in-del | -/C | 0.0019996 | 0.0315563 | frameshift-variant | RAB40C | GRCh38.p7 | 16:627579 | CCGTCCACCCCAGAG[-/C]CCCCCCCCAGAACTG | 57799 |
| rs769861385 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593725 | CAGCACCTGTGGGAG[C/T]CCCTGTGAGCTCTTC | 57799 |
| rs769864220 | snp | C/T | 3.34538e-05 | 0.00408971 | intron-variant | RAB40C | GRCh38.p7 | 16:617161 | GGTCTCGCGGGCGCT[C/T]GCTCCAGGAGTGGCG | 57799 |
| rs769909352 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:600497 | GTGGCTCACGCCTGT[A/G]ATCCCAGCACTTTGG | 57799 |
| rs769916923 | snp | A/G | 4.94964e-05 | 0.00497451 | missense | RAB40C | GRCh38.p7 | 16:627422 | AAGCTTCCACTGCCC[A/G]TCACCATCAAGAGCC | 57799 |
| rs770019388 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:620257 | AATTAGCCGAGCATG[A/G]TGGCGGGCGCTTATA | 57799 |
| rs770089411 | in-del | -/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:607044 | CAGGTGGCCGAGGGT[-/C]CCACTTCCGAGCCGA | 57799 |
| rs770143530 | snp | A/C | 1.73078e-05 | 0.0029417 | intron-variant | RAB40C | GRCh38.p7 | 16:627327 | CCATGGTCTGACACC[A/C]CCTCTGCCCCACAGT | 57799 |
| rs770189402 | snp | A/G | 0.000164109 | 0.00905692 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629695 | GGGTGTGGACGCCCC[A/G]GAGGTCACAGCTGAG | 57799 |
| rs770337836 | snp | A/C | 5.17451e-05 | 0.00508624 | utr-variant-5-prime | RAB40C | GRCh38.p7 | 16:590279 | GCCGGCGCGGGGCGC[A/C]GGCGGCGCGGCCATG | 57799 |
| rs770378739 | snp | C/T | 9.99467e-05 | 0.00706848 | synonymous-codon | RAB40C | GRCh38.p7 | 16:627541 | CGGCAGCAAGGGCAA[C/T]AGCCTCAAGAGGTCC | 57799 |
| rs770397003 | snp | C/G | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593631 | ACATTGCCCTCTCCA[C/G]CTTCACAAACAAATG | 57799 |
| rs770515259 | snp | C/T | 0.000379403 | 0.013768 | synonymous-codon | RAB40C | GRCh38.p7 | 16:627463 | CTTCTCGATGGCCAA[C/T]GGCATGAACGCGGTC | 57799 |
| rs770549449 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:618126 | GACATCCAGGTGGGT[C/T]GGCAGAGGAGGGAAG | 57799 |
| rs770551364 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:603699 | CACATATATGTACCT[A/G]TGCAGCCAGTACCCT | 57799 |
| rs770590817 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:592552 | GCCTCCTGGTCCTGC[A/C]CTTGACAGTGACTGC | 57799 |
| rs770666326 | snp | A/G | | | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:598462 | ACTACTTGGGAGGCT[A/G]AGGCAGGAGAATTGC | 57799 |
| rs770692706 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:623886 | GCAGTGAGCCATGAT[C/T]GTGCCACTGCATGAA | 57799 |
| rs770759085 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:612405 | GCCGCCCTGGCCTGT[A/G]GAATCAAGAGCAAGG | 57799 |
| rs770780506 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:623315 | TGTCCATATAAACTT[C/T]TTCAGTGTAATGTGT | 57799 |
| rs770874166 | snp | C/T | 1.7249e-05 | 0.0029367 | intron-variant | RAB40C | GRCh38.p7 | 16:625549 | CCCGGGGAAGGCAGG[C/T]TGGATGGAGGTACCT | 57799 |
| rs770929145 | snp | C/G | 1.66827e-05 | 0.00288809 | missense | RAB40C | GRCh38.p7 | 16:625984 | CGGAGCAGGCCCGCG[C/G]GTACGCAGAGAAGAA | 57799 |
| rs771006291 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:602554 | TTGCCTCAGCCCCCC[A/G]AGTAGCTGGGATTAC | 57799 |
| rs771019645 | snp | C/G | 1.98088e-05 | 0.00314707 | missense | RAB40C | GRCh38.p7 | 16:590415 | GGCGCGGCAGAGTCC[C/G]CGTACGCCTACAGTA | 57799 |
| rs771041462 | in-del | -/CT | | | intron-variant | RAB40C | GRCh38.p7 | 16:606080 | TAGATGGCCTTTCTA[-/CT]CCTTTTCTGTTATTG | 57799 |
| rs771075244 | snp | A/G | 0.000187213 | 0.00967324 | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596334 | TGCAGCTGAGAAGGC[A/G]CGAAGCTGCTGGTCC | 57799 |
| rs771251211 | snp | A/G | 1.68292e-05 | 0.00290075 | intron-variant | RAB40C | GRCh38.p7 | 16:618311 | AGGATGTTTCTCCTG[A/G]TTCTTTCTGAATGTG | 57799 |
| rs771259707 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:619931 | CTGGGTCGCACCCTG[C/T]CCTGGGAGTTCCCTC | 57799 |
| rs771325209 | snp | C/T | 1.66804e-05 | 0.00288789 | synonymous-codon | RAB40C | GRCh38.p7 | 16:618218 | CACGTCGGGCCAGGG[C/T]CGGTTCTGCACCATC | 57799 |
| rs771341059 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:591491 | ACGCTGTTCCCCTGA[A/G]GTATTTGCTTACTGC | 57799 |
| rs771378762 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:590644 | GAGGACGGACCAGAG[A/G]GACGCGCCCAGCGGG | 57799 |
| rs771478109 | snp | A/G/T | 3.41987e-05 | 0.00413502 | intron-variant | RAB40C | GRCh38.p7 | 16:625537 | CCGGGGAGCCCTCCC[A/G/T]GGGAAGGCAGGCTGG | 57799 |
| rs771499215 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:622220 | TTATCGTGTAGGTCG[A/C]GTTGATCAAAAAAAG | 57799 |
| rs771589776 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:600127 | TGGGACTCCCATGGC[C/T]CCCTTGATGTTGGAG | 57799 |
| rs771616751 | snp | C/T | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628301 | CCAAATCCCTCCCCA[C/T]GTGGGGATGAGAACC | 57799 |
| rs771689887 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:627123 | AGCAGCACCGCCCAG[C/T]GTGCCTGGCTTTAGG | 57799 |
| rs771714973 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:592655 | GCTTGGCTCCAGGGG[C/T]GCTGCGCACTCCCAG | 57799 |
| rs771723562 | snp | A/G | | | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596073 | GCACTTGCTCTAAGC[A/G]CTCACAGGCAACAGG | 57799 |
| rs771752236 | snp | C/T | 2.01721e-05 | 0.00317579 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627669 | CAGGAGGGCTCGAGC[C/T]GGACACTCCTGGCTG | 57799 |
| rs771753462 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:608186 | GGAAGGTACCTCACA[C/T]AGGGCAGCTCCAGAG | 57799 |
| rs771905582 | in-del | -/TTA | | | intron-variant | RAB40C | GRCh38.p7 | 16:623346 | TGTGTGTTCATACTT[-/TTA]TTTTTTAAAAATCAT | 57799 |
| rs771906342 | snp | A/T | 1.64991e-05 | 0.00287215 | missense | RAB40C | GRCh38.p7 | 16:627467 | TCGATGGCCAACGGC[A/T]TGAACGCGGTCATGA | 57799 |
| rs771987720 | snp | C/T | 3.33039e-05 | 0.00408055 | synonymous-codon | RAB40C | GRCh38.p7 | 16:625476 | CCGCTGGTCCTTTGA[C/T]GGCATCGACCGCTGG | 57799 |
| rs771998376 | snp | A/G | 0.000492005 | 0.0156767 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629687 | GCCCAGGGGGGTGTG[A/G]ACGCCCCGGAGGTCA | 57799 |
| rs772079882 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:602688 | TCCACCCACCTCGGC[C/T]TCCCAAAGTGCTGGG | 57799 |
| rs772126157 | snp | A/G | 1.66941e-05 | 0.00288908 | missense | RAB40C | GRCh38.p7 | 16:626110 | TGGAGAAGATCTGGA[A/G]GCCCAACCGAGGTGG | 57799 |
| rs772193319 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:602224 | GGAATGAAATATATG[A/G]CAACATTAGCAGTGG | 57799 |
| rs772222679 | snp | A/G | 1.66109e-05 | 0.00288187 | missense | RAB40C | GRCh38.p7 | 16:626004 | GCAGAGAAGAACTGC[A/G]TGACCTTCTTTGAGG | 57799 |
| rs772359753 | in-del | -/C | 0.000163385 | 0.00903692 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629648 | CCGCCTGCACGCTGG[-/C]CAATCTGGTGTCTGC | 57799 |
| rs772371759 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:610593 | AGAGAATATGTCACA[C/G]CTGATGCCTAGGGAC | 57799 |
| rs772545151 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:600621 | CTTGGCCTGGTGGCA[G/T]GCACCTGTATTCCCA | 57799 |
| rs772550240 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:602702 | CCTCCCAAAGTGCTG[C/G]GATTACAGGCGTGAG | 57799 |
| rs772590683 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:620249 | AATACAAAAATTAGC[C/T]GAGCATGGTGGCGGG | 57799 |
| rs772591183 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:592014 | CAGAGTGAGTGAGAC[A/G]GTGTGGTCCTCATCC | 57799 |
| rs772649673 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594910 | CTGCAACCTCTGCCT[C/T]CTGGGTTCAAGTGAT | 57799 |
| rs772787623 | snp | A/G/T | 4.99599e-05 | 0.00499779 | missense | RAB40C | GRCh38.p7 | 16:627540 | GCGGCAGCAAGGGCA[A/G/T]CAGCCTCAAGAGGTC | 57799 |
| rs772800098 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:617138 | CTGGGAGGCCAGTGG[C/T]CGAGGCTGGTCTCGC | 57799 |
| rs772828486 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:623186 | CATCAGCCGGGAGGC[A/G]GGCCTTCTGCTCTCT | 57799 |
| rs772978054 | snp | A/G | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596729 | CAGCTGTGGGAAGAA[A/G]GACTGGCTGCCAAGA | 57799 |
| rs773009600 | snp | A/G | 6.66278e-05 | 0.00577143 | missense | RAB40C | GRCh38.p7 | 16:625483 | TCCTTTGACGGCATC[A/G]ACCGCTGGATCAAGG | 57799 |
| rs773024861 | in-del | -/T | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587805 | TATTTTTGAGGCACT[-/T]TTTTTTTTTTTTTTT | 57799 |
| rs773047822 | snp | C/T | 3.3054e-05 | 0.00406521 | synonymous-codon | RAB40C | GRCh38.p7 | 16:617242 | CACCATCCTGCTGGA[C/T]GGCCGGCGCGTGAAG | 57799 |
| rs773197492 | in-del | -/T | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593729 | ACCTGTGGGAGCCCC[-/T]GTGAGCTCTTCCGTG | 57799 |
| rs773206784 | snp | C/T | 1.66007e-05 | 0.00288098 | synonymous-codon | RAB40C | GRCh38.p7 | 16:626009 | GAAGAACTGCATGAC[C/T]TTCTTTGAGGTCAGC | 57799 |
| rs773264668 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:623388 | GGCGCGGTGGCTCAC[A/G]CCTGTCATCCCAGCA | 57799 |
| rs773284202 | snp | A/G | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628484 | TCGGCAGCTTCTGTC[A/G]CTGGCCCTGGGGTCC | 57799 |
| rs773288553 | in-del | -/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:626549 | TCCCGTGAAGCCCCC[-/C]TCAGGGAGGTGGTAC | 57799 |
| rs773289996 | snp | C/T | 1.79374e-05 | 0.00299472 | synonymous-codon | RAB40C | GRCh38.p7 | 16:590324 | TCCGGTGAAGAGCTA[C/T]GACTACCTGCTCAAG | 57799 |
| rs773315300 | in-del | -/AATAAA | | | intron-variant | RAB40C | GRCh38.p7 | 16:602428 | CCTGGCTAATTTTTT[-/AATAAA]TTATTTTTTTATTTT | 57799 |
| rs773407703 | snp | C/T | 1.67192e-05 | 0.00289125 | synonymous-codon | RAB40C | GRCh38.p7 | 16:626114 | GAAGATCTGGAGGCC[C/T]AACCGAGGTGGGTGG | 57799 |
| rs773462982 | snp | C/G | | | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596090 | TCACAGGCAACAGGG[C/G]AAATGCTTGCATGGC | 57799 |
| rs773521949 | snp | A/G | 1.95421e-05 | 0.00312581 | synonymous-codon | RAB40C | GRCh38.p7 | 16:590411 | GGACGGCGCGGCAGA[A/G]TCCCCGTACGCCTAC | 57799 |
| rs773588766 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:621309 | GCATCCAGCCGAGGT[G/T]CAGAGCCCAGGTTTG | 57799 |
| rs773682689 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:613824 | GGCCTTGGTGGGGGT[C/T]GTGGGCAGCACCCAG | 57799 |
| rs773729382 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:617501 | GGAAAACCTGATTCC[A/G]TGGTGGCTGTGAGCC | 57799 |
| rs773772464 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:624620 | CAGCCTCAGCCTCTT[A/G]TGTGATAGGCTCTTC | 57799 |
| rs773870979 | snp | C/T | 1.66474e-05 | 0.00288503 | missense | RAB40C | GRCh38.p7 | 16:625462 | TATGACATCACCAAC[C/T]GCTGGTCCTTTGACG | 57799 |
| rs773993134 | in-del | -/GACAGAAC | | | intron-variant | RAB40C | GRCh38.p7 | 16:609094 | CACTCCAGCCTGGGT[-/GACAGAAC]GAGACACCTTCTCAA | 57799 |
| rs774028554 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:591921 | TTTTAACTTCCAGTG[G/T]CATGGCTAAAATACA | 57799 |
| rs774095767 | snp | G/T | | | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595970 | GAAACTGTTGAGTCA[G/T]TAGGTAGAATATTGA | 57799 |
| rs774189137 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594704 | TGTGTCTTTAGGTGA[C/T]TGGACAGCCGTGCGT | 57799 |
| rs774200663 | snp | C/T | 1.66117e-05 | 0.00288194 | missense | RAB40C | GRCh38.p7 | 16:627368 | CAGGACCTCTGCTGC[C/T]GGGCCATCGTCTCCT | 57799 |
| rs774385943 | in-del | -/AAAAC | | | intron-variant | RAB40C | GRCh38.p7 | 16:626938 | CGAGACCCGTCTCAA[-/AAAAC]AAAACAAAAGAATGA | 57799 |
| rs774487819 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:601978 | TGAAAATATAAAAGT[G/T]AGCGGGGTGTGGTGT | 57799 |
| rs774511525 | in-del | -/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:622548 | GGTCTGGCTCTGTCG[-/C]CCAGGCTGGAGTGCC | 57799 |
| rs774539851 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:610445 | GAGTTGCTGGTGCTG[C/T]GTGAGGCCTCAGTGG | 57799 |
| rs774680458 | snp | A/G | 1.66313e-05 | 0.00288364 | missense | RAB40C | GRCh38.p7 | 16:625993 | CCCGCGCGTACGCAG[A/G]GAAGAACTGCATGAC | 57799 |
| rs774786022 | snp | A/G | 4.94939e-05 | 0.00497439 | synonymous-codon | RAB40C | GRCh38.p7 | 16:627454 | CCTCAAGTCCTTCTC[A/G]ATGGCCAACGGCATG | 57799 |
| rs774803972 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:623991 | TTCTTACCTCACCTG[G/T]GTTGCACATCTCTCC | 57799 |
| rs774827212 | snp | C/T | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628918 | CCCAAGGTGGTCCCA[C/T]GGAGGGTGTTACTGG | 57799 |
| rs774905581 | snp | C/G | 4.95962e-05 | 0.00497952 | synonymous-codon | RAB40C | GRCh38.p7 | 16:617230 | CTACAAGACCACCAC[C/G]ATCCTGCTGGACGGC | 57799 |
| rs774909313 | snp | C/G | 1.95911e-05 | 0.00312973 | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:627659 | GTGCAGATGCCAGGA[C/G]GGCTCGAGCTGGACA | 57799 |
| rs774943711 | snp | A/G | 1.66588e-05 | 0.00288602 | intron-variant | RAB40C | GRCh38.p7 | 16:618266 | GGGCGCTCAGGTAAG[A/G]CCAGCACCGCTCTTT | 57799 |
| rs774947503 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:598830 | GTTTGTACAGCGGCC[A/G]GATGTAAGAACCTCA | 57799 |
| rs774998808 | snp | C/G | 4.86606e-05 | 0.00493234 | intron-variant | RAB40C | GRCh38.p7 | 16:625036 | AAATGCCCCCACTCA[C/G]CTCTGTCCCAGGTAC | 57799 |
| rs775037236 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:600612 | AAAAATTAGCTTGGC[C/G]TGGTGGCATGCACCT | 57799 |
| rs775071660 | in-del | -/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:598781 | GATGGAAGAAGAGAA[-/G]AGCTGAGTCCTGGAA | 57799 |
| rs775076694 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:600773 | ATAAAAATAAGAGCT[C/T]TGGTGCCTACGTGCG | 57799 |
| rs775310196 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:613705 | TTTTTTTCCCCAGAG[G/T]ATAGTTTGTCTTTAG | 57799 |
| rs775383195 | snp | A/G | 2.26585e-05 | 0.00336582 | missense | RAB40C | GRCh38.p7 | 16:590304 | GCCATGGGCTCGCAG[A/G]GCAGTCCGGTGAAGA | 57799 |
| rs775448443 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:605957 | GATGGCTGCAAGCTT[G/T]TTTCTTTGTAATAGC | 57799 |
| rs775459220 | snp | G/T | 1.78643e-05 | 0.00298862 | missense | RAB40C | GRCh38.p7 | 16:627613 | GCGGAGTAACTGCAA[G/T]ATCTCCTAGCGGGGA | 57799 |
| rs775492767 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:624587 | CCTAATTTTCAGATG[G/T]ACAGTGCCCTCTTCT | 57799 |
| rs775507503 | snp | C/T | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:597340 | AGCAGCCTTCGCCGT[C/T]TTTACAGTGAACACA | 57799 |
| rs775514246 | snp | A/G | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593764 | CTAATGTGGGTGTGC[A/G]CTGGGTTTCTGGATC | 57799 |
| rs775603912 | snp | G/T | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594617 | GAGGCTCCTCCGTGT[G/T]TCATTGTCCTGATGT | 57799 |
| rs775624835 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:622162 | AAAAATGATAGCAAA[A/C]AGGACACCCACTCTT | 57799 |
| rs775652595 | snp | A/G | 1.69106e-05 | 0.00290775 | intron-variant | RAB40C | GRCh38.p7 | 16:626136 | GGTGGGTGGGCGGGC[A/G]CCGGCCAGCCCTGAG | 57799 |
| rs775847327 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:622298 | CGCAGTACCAGTTCA[C/T]GAGCAGGCGGGGGTG | 57799 |
| rs775870936 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:618359 | ACTCCCAAGGACTTT[C/G]TTTCTTTATAAGGAT | 57799 |
| rs775885600 | in-del | -/AA | | | intron-variant | RAB40C | GRCh38.p7 | 16:601816 | CCTGCAAAAAAAAGT[-/AA]AAAAAAAAAAAAAAA | 57799 |
| rs776025146 | in-del | -/TCA | | | intron-variant | RAB40C | GRCh38.p7 | 16:607789 | GAGCAAGACTCCGTC[-/TCA]AAAACGAAAAGAAAA | 57799 |
| rs776054579 | snp | C/T | 6.91467e-05 | 0.00587951 | intron-variant | RAB40C | GRCh38.p7 | 16:627328 | CATGGTCTGACACCC[C/T]CTCTGCCCCACAGTG | 57799 |
| rs776109808 | snp | A/G | 3.3451e-05 | 0.00408954 | intron-variant | RAB40C | GRCh38.p7 | 16:617162 | GTCTCGCGGGCGCTC[A/G]CTCCAGGAGTGGCGC | 57799 |
| rs776136791 | snp | A/G | 1.76263e-05 | 0.00296864 | missense | RAB40C | GRCh38.p7 | 16:627603 | AGAACTGCTCGCGGA[A/G]TAACTGCAAGATCTC | 57799 |
| rs776140672 | snp | A/T | 1.67089e-05 | 0.00289035 | stop-gained | RAB40C | GRCh38.p7 | 16:627548 | AAGGGCAACAGCCTC[A/T]AGAGGTCCAAGTCCA | 57799 |
| rs776158624 | in-del | -/GAGT | | | intron-variant | RAB40C | GRCh38.p7 | 16:623919 | CCAGCCTGGCTGACA[-/GAGT]GAGACCCTGTTTCAA | 57799 |
| rs776193746 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593653 | AAACAAATGAGTCAT[C/T]GAAGTGACCTTTTTC | 57799 |
| rs776239646 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:610623 | CCCCCTTATGGGGTA[A/G]TGTTGAGCTCTGCAG | 57799 |
| rs776330109 | snp | C/G | 1.73543e-05 | 0.00294565 | intron-variant | RAB40C | GRCh38.p7 | 16:618178 | CCACAGTCCCGGCCC[C/G]TCCCCTCCCCGTATG | 57799 |
| rs776452781 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:623911 | CATGAACCCCAGCCT[A/G]GCTGACAGAGTGAGA | 57799 |
| rs776473772 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:592909 | CCTCTGACATGCTCA[C/G]TGAAGTGGGGCCAGT | 57799 |
| rs776529249 | snp | G/T | 1.65556e-05 | 0.00287707 | intron-variant | RAB40C | GRCh38.p7 | 16:625853 | CTGCGGCTGAGGGGT[G/T]GGTGGCACCCTGCGT | 57799 |
| rs776538058 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:623341 | TGTGTTGTGTGTTCA[C/T]ACTTTTATTTTTTAA | 57799 |
| rs776567548 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:604010 | GGTTATTTCCTGGTT[G/T]GGGGTATTACGAATA | 57799 |
| rs776689384 | snp | A/G | | | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596149 | TCGCAGGGTGGTGTG[A/G]ACACAGATGACTCGT | 57799 |
| rs776707656 | snp | C/T | 1.67377e-05 | 0.00289284 | intron-variant | RAB40C | GRCh38.p7 | 16:617157 | GGCTGGTCTCGCGGG[C/T]GCTCGCTCCAGGAGT | 57799 |
| rs776721781 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:607250 | CCCTGTCATCCCAGC[A/G]CTTTGGGAGGCCGAG | 57799 |
| rs776780379 | snp | A/G | 4.94035e-05 | 0.00496984 | utr-variant-5-prime | RAB40C | GRCh38.p7 | 16:590280 | CCGGCGCGGGGCGCA[A/G]GCGGCGCGGCCATGG | 57799 |
| rs776788379 | in-del | -/TC | | | intron-variant | RAB40C | GRCh38.p7 | 16:606786 | TGCTTTGACTCTCCT[-/TC]TGTCTCATCTGTAGC | 57799 |
| rs776802883 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:622266 | GATGCATATTGCCAC[C/T]GTTACCCAAGAGCTG | 57799 |
| rs776811555 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:621524 | CACACAGCAGCAGTC[C/T]CGCGGCTCTTCCCGC | 57799 |
| rs776850000 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:590704 | ACGGTGTCACGGGTC[C/G]GGGATCTCAGGGGAA | 57799 |
| rs776894595 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:626463 | GCTGTCAGGGGAGCA[C/T]AGGAGCCGTGCCTGC | 57799 |
| rs776983204 | in-del | -/ATT | | | intron-variant | RAB40C | GRCh38.p7 | 16:600436 | TGCCGAGTTTAAAAC[-/ATT]GTTGTTGGACTTTTT | 57799 |
| rs776993944 | snp | A/G | 4.95037e-05 | 0.00497488 | synonymous-codon | RAB40C | GRCh38.p7 | 16:627475 | CAACGGCATGAACGC[A/G]GTCATGATGCACGGC | 57799 |
| rs777101065 | snp | C/T | 3.34163e-05 | 0.00408742 | synonymous-codon | RAB40C | GRCh38.p7 | 16:625982 | GACGGAGCAGGCCCG[C/T]GCGTACGCAGAGAAG | 57799 |
| rs777119754 | snp | A/G | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:587951 | TAGCTGGGATTACAG[A/G]CACGTACCAACATGC | 57799 |
| rs777133072 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:591749 | GGTGTATGCCACCAC[A/G]CCCGGCTAATTTTGT | 57799 |
| rs777343433 | snp | A/G | 9.94777e-05 | 0.00705188 | synonymous-codon | RAB40C | GRCh38.p7 | 16:626060 | CATCGAGTCCTTCAC[A/G]GAGCTATCCCGCATC | 57799 |
| rs777414099 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:609151 | GGACTGATAGGTGAG[A/C]GAGGTTTGATGGTTT | 57799 |
| rs777469578 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:627198 | GCAGAGAAGTTTGGG[C/T]GTCCAGGTCCTCCAG | 57799 |
| rs777487194 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:604589 | TTTCTCTAGAATACA[C/T]GTGAGTCCTTCTGAA | 57799 |
| rs777533671 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:615226 | TTCGATGCATGAGAA[C/T]AGCCTTTGATGTACA | 57799 |
| rs777544608 | snp | G/T | 1.75093e-05 | 0.00295877 | missense | RAB40C | GRCh38.p7 | 16:590383 | GCAAGGGCGAGATCC[G/T]GGAGAGCCTGCAGGA | 57799 |
| rs777586712 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:616960 | GCCCGATGGCCTGAC[A/G]CTGTATGGACCACGC | 57799 |
| rs777681427 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:602515 | TTGGCTCACTGCAAC[A/G]TCTGCCTCCTGGGTT | 57799 |
| rs777748966 | in-del | -/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:605835 | GGCTGTAGGGCCTGT[-/G]GTAGATGCTGCCAAC | 57799 |
| rs777766261 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:619809 | GGACACTGGAGCTTC[A/G]TCCCATGGCAAGCTC | 57799 |
| rs777773126 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:615414 | GCACTCCGTGGGAGG[G/T]CGTCGCTTATGTTTA | 57799 |
| rs777858212 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:618025 | CCTGGCTCAGCGGCA[C/T]GGCGCCAGGCTGCTG | 57799 |
| rs778009841 | snp | A/C | 1.77439e-05 | 0.00297853 | intron-variant | RAB40C | GRCh38.p7 | 16:627301 | TGCACAGGGCCTCCT[A/C]CCCCACAGCCCCATG | 57799 |
| rs778264724 | snp | C/T | | | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:598047 | GTCAAGAGATTGAGA[C/T]CATCCTGGCCAACAT | 57799 |
| rs778294513 | snp | A/G | 3.34521e-05 | 0.00408961 | synonymous-codon | RAB40C | GRCh38.p7 | 16:618209 | TTTCAGGGACACGTC[A/G]GGCCAGGGCCGGTTC | 57799 |
| rs778363515 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:603166 | GCTCTTTGTAGACAC[A/G]AGAGCCCTTTTGGCT | 57799 |
| rs778542482 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:607005 | AGACAGACAGACTAC[C/G]ACCTGAGCCAAGGAA | 57799 |
| rs778611041 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:622807 | CGGCGCCTGGCCGAA[A/G]TCGCTAGTTTTTTAA | 57799 |
| rs778626563 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:617054 | CTGGGCCAGAGCCCC[A/G]AGATTTCCCCCTGCC | 57799 |
| rs778630316 | snp | C/G | 1.65083e-05 | 0.00287296 | synonymous-codon | RAB40C | GRCh38.p7 | 16:627400 | CACCCCCGTGCACCT[C/G]ATCGACAAGCTTCCA | 57799 |
| rs778642317 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:603405 | TCTCAGAAGACATCC[A/G]AGGGGAGTGGTATGC | 57799 |
| rs778661347 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:613983 | AGATGCTTCCAAAAT[A/G]TCTGCAAGGCTGCGG | 57799 |
| rs778662024 | in-del | -/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:626756 | CAGCCTGGCCAACAC[-/G]GTGAAACCCCGTCTC | 57799 |
| rs778692638 | snp | C/T | 5.04944e-05 | 0.00502441 | missense | RAB40C | GRCh38.p7 | 16:625966 | TCAAGCGGCAGGTCC[C/T]GACGGAGCAGGCCCG | 57799 |
| rs778796745 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:610608 | GCTGATGCCTAGGGA[A/C]CCCCTTATGGGGTAG | 57799 |
| rs778802772 | in-del | -/TT | | | intron-variant | RAB40C | GRCh38.p7 | 16:602188 | TATATGCTTGATATC[-/TT]AAGTATGTAAAATAA | 57799 |
| rs778849580 | in-del | -/TTTTC | | | intron-variant | RAB40C | GRCh38.p7 | 16:591578 | ATTTGTTTTGTTTTG[-/TTTTC]TTTTCTTTTCTTTCT | 57799 |
| rs778861706 | in-del | -/AT | | | intron-variant | RAB40C | GRCh38.p7 | 16:601346 | TGTTAGAGGTGTTAC[-/AT]ATTTGCCCTAGGTGG | 57799 |
| rs779085705 | snp | A/G | 6.85601e-05 | 0.00585451 | intron-variant | RAB40C | GRCh38.p7 | 16:618189 | GCCCCTCCCCTCCCC[A/G]TATGTTTCAGGGACA | 57799 |
| rs779095249 | snp | A/G | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593508 | GGAGGCCCCTTCTGT[A/G]CAAGGCTTACTGCTT | 57799 |
| rs779122195 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:601216 | ACCAAAAACTATGAT[C/T]TTTTGTGTGTTATCC | 57799 |
| rs779138528 | in-del | -/A | 1.72337e-05 | 0.00293539 | frameshift-variant | RAB40C | GRCh38.p7 | 16:627586 | CCCCAGAGCCCCCCC[-/A]CAGAACTGCTCGCGG | 57799 |
| rs779192205 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:623736 | AGGATCACTTGAGGC[C/T]AGGGGTTCAAGACCA | 57799 |
| rs779225337 | snp | A/C | | | utr-variant-5-prime | RAB40C | GRCh38.p7 | 16:590266 | GCTTCGGCAGGCGGC[A/C]GGCGCGGGGCGCAGG | 57799 |
| rs779300314 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:591182 | CTCAGGGGAAGGTGT[C/T]ATGGGCCTAAGGGAA | 57799 |
| rs779398914 | in-del | -/TG | | | intron-variant | RAB40C | GRCh38.p7 | 16:619204 | GTGCACTCAGGGCCA[-/TG]TGTGTGTGCAGGCAT | 57799 |
| rs779487429 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:615321 | GTAGGCAGAGAGACC[A/G]CATGGCTGGCTTGCA | 57799 |
| rs779526870 | in-del | -/G | 0 | 0 | intron-variant | RAB40C | GRCh38.p7 | 16:625055 | GTCCCAGGTACTCCC[-/G]GGGGGGATTCACTGA | 57799 |
| rs779601647 | snp | C/T | 1.72337e-05 | 0.00293539 | synonymous-codon | RAB40C | GRCh38.p7 | 16:627586 | ACCCCAGAGCCCCCC[C/T]CAGAACTGCTCGCGG | 57799 |
| rs779662868 | snp | C/T | 0.000326531 | 0.0127734 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629642 | GCAGAGCCGCCTGCA[C/T]GCTGGCCAATCTGGT | 57799 |
| rs779666099 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:621105 | TTTTCCACATGCGAG[C/G]AGCAGGTTACAGACC | 57799 |
| rs779670772 | snp | A/G | 1.66435e-05 | 0.0028847 | synonymous-codon | RAB40C | GRCh38.p7 | 16:626099 | GCGGCACGGCATGGA[A/G]AAGATCTGGAGGCCC | 57799 |
| rs779679017 | snp | A/G | | | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629697 | GTGTGGACGCCCCGG[A/G]GGTCACAGCTGAGCT | 57799 |
| rs779693932 | snp | A/G | | | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595883 | TGGGATTACAAGGGT[A/G]AGCCACTGTGCCTGG | 57799 |
| rs779696713 | in-del | -/GGTCCCCGCGGCCTG | | | intron-variant | RAB40C | GRCh38.p7 | 16:621437 | TGGAGAGGCCTGGAA[-/GGTCCCCGCGGCCTG]GGTCTTGCAGATGGC | 57799 |
| rs779717992 | snp | C/T | 1.67576e-05 | 0.00289457 | intron-variant | RAB40C | GRCh38.p7 | 16:625412 | AGTGACCCCTGATGA[C/T]CCCCAAGTCTCTGTT | 57799 |
| rs779783816 | snp | A/C/T | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596466 | ACGATGCCACCCCAC[A/C/T]GAGGGCCGTTCTGGG | 57799 |
| rs779856204 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:626841 | TATTCGGGAGGCTGA[A/G]GCAGGAGAATCGCTT | 57799 |
| rs779858421 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:617308 | GTTCCTGGGTGAGGA[C/T]ACAAATGCCGAAGGG | 57799 |
| rs779871097 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:608058 | ATGTACTCACCTGTT[C/G]TCACGCTGCTAGGAA | 57799 |
| rs779921292 | snp | C/G | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628076 | TCGCGGCCGCGATGG[C/G]AAGGCATCCTGTGAA | 57799 |
| rs779964361 | snp | A/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:591072 | ATCTGGGGGAAGGCA[A/T]CATGGTCCTAAGGGA | 57799 |
| rs780004811 | snp | A/G | 1.85761e-05 | 0.00304758 | synonymous-codon | RAB40C | GRCh38.p7 | 16:590405 | CCTGCAGGACGGCGC[A/G]GCAGAGTCCCCGTAC | 57799 |
| rs780137154 | snp | A/G | 1.65715e-05 | 0.00287845 | synonymous-codon | RAB40C | GRCh38.p7 | 16:627520 | GGCCAGCGGGGCCGG[A/G]GGCGGCGGCAGCAAG | 57799 |
| rs780192394 | snp | C/T | 1.65269e-05 | 0.00287457 | intron-variant | RAB40C | GRCh38.p7 | 16:617286 | GAGTTGGGGCTGCGG[C/T]ACTTCAGTTCCTGGG | 57799 |
| rs780203124 | snp | C/G | 6.543e-05 | 0.00571933 | intron-variant | RAB40C | GRCh38.p7 | 16:590473 | CTGCTACGCGGGGCC[C/G]GAGCCCGGCGAGCTG | 57799 |
| rs780261827 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:600513 | ATCCCAGCACTTTGG[C/G]AGGCCGAGGCGGGCG | 57799 |
| rs780318222 | snp | G/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:613765 | CTTAGTGGGAGTCGT[G/T]GGCAACACCCAGGTC | 57799 |
| rs780324010 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:623053 | GCCATCGCCCCTGCC[C/T]GTAACCCCTACTCCT | 57799 |
| rs780345980 | snp | A/G | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628878 | GACCCAGGACCCCCC[A/G]TGGTGGACTCCGCGG | 57799 |
| rs780349837 | snp | A/G | | | upstream-variant-2KB | RAB40C | GRCh38.p7 | 16:588134 | TTATGTTCTCAGGAA[A/G]GGAGGAGACGGCTGC | 57799 |
| rs780372782 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:622999 | GTCCCTGCGGCCTCA[A/C]TGTGACCCACGCCGG | 57799 |
| rs780459173 | in-del | -/AG | | | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595719 | TGATTCTACTGCCTC[-/AG]AGCCTCCCGAGTAGC | 57799 |
| rs780469810 | snp | A/G | 1.64991e-05 | 0.00287215 | missense | RAB40C | GRCh38.p7 | 16:627425 | CTTCCACTGCCCGTC[A/G]CCATCAAGAGCCACC | 57799 |
| rs780470941 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593209 | TGCCAACCTCAGGGG[C/T]CAGCCCTCTTCATCA | 57799 |
| rs780560716 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594081 | TTCCCCAAGCCCAGC[C/T]GCTCCCGCTCTGCAG | 57799 |
| rs780638342 | in-del | -/GTGGCATCAGTCAGCGTGGATTTGCAAGGTTTTGTTACCTC | | | intron-variant | RAB40C | GRCh38.p7 | 16:599672 | AGGTTTTGTTCCCTT[lengthTooLong]GTGGCATCAGTCAGC | 57799 |
| rs780831489 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:600423 | ATGTCACCTAACCTG[C/T]CGAGTTTAAAACATT | 57799 |
| rs780951373 | snp | A/G | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:594082 | TCCCCAAGCCCAGCC[A/G]CTCCCGCTCTGCAGG | 57799 |
| rs781008758 | in-del | -/A | | | intron-variant | RAB40C | GRCh38.p7 | 16:623637 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 57799 |
| rs781221406 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:604344 | ACTATAACACAAATA[C/T]GCACGAGGCCTTCTG | 57799 |
| rs781285491 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:605364 | AATCAGCTTTATTGA[A/G]GTGTAATTTGTGTAC | 57799 |
| rs781305739 | snp | A/G | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593117 | TCTGGGCTGTGGAAC[A/G]CGCTTTCTGTGTCTA | 57799 |
| rs781312299 | snp | A/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:603229 | CTAGCTTCGCAGGAA[A/T]CCAGTCCACAAACTG | 57799 |
| rs781346168 | in-del | -/T | 3.52162e-05 | 0.00419605 | intron-variant | RAB40C | GRCh38.p7 | 16:625559 | CAGGCTGGATGGAGG[-/T]TACCTGGGCCCCGGG | 57799 |
| rs781376231 | snp | A/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:610061 | CAGGCCAGGGCCAGA[A/T]GTAGCCTCATACCAG | 57799 |
| rs781402394 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:602585 | AGGCACCTGCCACCA[C/T]GCCCGGCTAGTTTTT | 57799 |
| rs781402486 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:616807 | CCTTTCTCCAGGCAC[A/G]CTGGAGTCCACGCCC | 57799 |
| rs781409446 | snp | A/G | | | utr-variant-3-prime | RAB40C | GRCh38.p7 | 16:628003 | CGGTGGTGGTGCACT[A/G]GTGACTTCATGGCCA | 57799 |
| rs781419176 | snp | C/T | 1.67964e-05 | 0.00289792 | intron-variant | RAB40C | GRCh38.p7 | 16:625403 | ATGCGTGTCAGTGAC[C/T]CCTGATGACCCCCAA | 57799 |
| rs781442042 | in-del | -/CTGGGT | | | intron-variant | RAB40C | GRCh38.p7 | 16:619683 | GCCCAGGGAGGCCGC[-/CTGGGT]CTGGGTCTGGGTCTG | 57799 |
| rs781461416 | snp | A/G | 3.31439e-05 | 0.00407073 | intron-variant | RAB40C | GRCh38.p7 | 16:617196 | CCCTCAGCGCCCTGT[A/G]CTTCCTCGCAGGGAT | 57799 |
| rs781474127 | snp | A/G | 0.000163092 | 0.00902882 | intron-variant, upstream-variant-2KB | RAB40C, WFIKKN1 | GRCh38.p7 | 16:629613 | CCAGGTCCTCCAGTC[A/G]GTCGGCCCGCTCAGC | 57799 |
| rs781573746 | snp | C/T | 0.000185512 | 0.00962919 | intron-variant | RAB40C | GRCh38.p7 | 16:624988 | TGGAGGGACTGGCAT[C/T]CTGCTCTGCAAGTTT | 57799 |
| rs781662144 | snp | A/C | | | intron-variant | RAB40C | GRCh38.p7 | 16:609266 | GTGCCTGGTGTGGTT[A/C]CCAGCAGGGAGCACA | 57799 |
| rs781683103 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:622930 | GTGCCGTTCGTTAGG[C/T]GGCTGCTGGTCACCG | 57799 |
| rs781726500 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:623511 | ACAAAAAAATTAGCC[A/G]GGCATGGTGGCGGGC | 57799 |
| rs781764780 | snp | A/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:622820 | AAGTCGCTAGTTTTT[A/T]AAAAATCAGATCAGT | 57799 |
| rs796104779 | in-del | -/A | | | intron-variant | RAB40C | GRCh38.p7 | 16:607502 | GAGTGAAACTGTCTC[-/A]AAAAAAAAAAAAAAC | 57799 |
| rs796107839 | snp | C/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:616164 | AGCAGGCTGAGGCTA[C/G]ATAATGGCGTGAACC | 57799 |
| rs796148252 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:607662 | CAGGCGCGGTGGTGG[A/G]CGCCTGTAGTCCCAG | 57799 |
| rs796337940 | in-del | -/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:590749 | GGGATCTGGAGCCCA[-/G]GGGAAGGTGTCATGG | 57799 |
| rs796347528 | snp | C/T | | | intron-variant, nc-transcript-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:596746 | ACTGGCTGCCAAGAC[C/T]ATGGGCTGTGGGCAT | 57799 |
| rs796354296 | in-del | -/A | | | intron-variant, downstream-variant-500B | RAB40C, LOC101929280 | GRCh38.p7 | 16:598391 | CAAAAAAAAAAAAAA[-/A]TACAAATACAAATAC | 57799 |
| rs796387451 | in-del | CGATGGTGAACTGCTAACTCTGCCGCATCCC/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:614317 | ACTCTGCCACATCCC[lengthTooLong]ATGGTGAACTGCCAA | 57799 |
| rs796625937 | snp | C/T | | | intron-variant | RAB40C, LOC101929280 | GRCh38.p7 | 16:595876 | AAAGTGCTGGGATTA[C/T]AAGGGTGAGCCACTG | 57799 |
| rs796773265 | snp | C/G | | | intron-variant, upstream-variant-2KB | RAB40C, LOC101929280 | GRCh38.p7 | 16:593794 | CTCTAGGTCTGGAAA[C/G]GCTTTCCTTTCTTTG | 57799 |
| rs796867285 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:601479 | GTGTGCTGAGCACCC[C/T]TGGGTGCCAGACTCC | 57799 |
| rs796918106 | snp | C/T | | | intron-variant | RAB40C | GRCh38.p7 | 16:607446 | AGGTAGAGGTTGCAG[C/T]GAGCTGATATTGCGC | 57799 |
| rs796925982 | multinucleotide-polymorphism | AGC/GGG | | | intron-variant | RAB40C | GRCh38.p7 | 16:616149 | TAGTTCAGCTACTCA[AGC/GGG]GGCTGAGGCTAGATA | 57799 |
| rs796981352 | snp | A/G | | | intron-variant | RAB40C | GRCh38.p7 | 16:627158 | AAGGCAGGGGATGGG[A/G]TGCCAGTGGACACAT | 57799 |