| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs186407737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47189248 | GTTTCCAGAGATAGC[A/G]ACTCTCCATAAAGTG | 10055 |
| rs186427880 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130608 | GCTGGGATCTCAGTA[C/T]GCACTCCTTAAATAT | 10055 |
| rs186430965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47148296 | GAATGGGAAGTGGGC[C/T]AGCTCATTTTCTTGG | 10055 |
| rs186470431 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47188613 | CTGGAAGATACTGCC[C/T]CAGGCACTCTTGGGT | 10055 |
| rs186494283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47147151 | GCAAAGCAAGGAAGG[C/T]GTGATCTGTGGACTG | 10055 |
| rs186518237 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47144246 | GGCTGAGGCACAAGA[A/T]TCGCTTGAATCTGGG | 10055 |
| rs186521117 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47174766 | TTTTAGTAGAGACGG[G/T]GTTTCACCATGTTAG | 10055 |
| rs186524929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47192543 | TCAGCCACCATGCCC[A/G]GCTACTTAATTTATT | 10055 |
| rs186538573 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SAE1 | GRCh38.p7 | 19:47134156 | GTGAGCCACCATGCC[C/T]GGCCTCAGATTTGTT | 10055 |
| rs186545911 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47185294 | ATCTGAATTTTTTTT[A/T]ATTTTTCATTTTTAT | 10055 |
| rs186552162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47152819 | CCAGAGAGACTGTTC[A/G]TTAAGATTTATTTAG | 10055 |
| rs186619542 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SAE1 | GRCh38.p7 | 19:47185495 | ATTTTTAGTGGACAC[A/G]AGGTTTCACCGTGTT | 10055 |
| rs186655103 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47182037 | GTGATCCTCCCACTT[C/T]TGCCTCCCAAAGCAT | 10055 |
| rs186676805 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47202306 | TTTATTTATTTATTT[A/T]TTGAGACAGTCTTGC | 10055 |
| rs186681217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47142182 | TGAGGTCAGGGGTTC[A/G]AGACCAGCCTGAACA | 10055 |
| rs186682260 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47158411 | GAGAAGATTTGAGAC[A/G]GATTTCGTCACAATC | 10055 |
| rs186710888 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47166888 | TTGTATACTATCTTT[A/T]ACAATGGATTTAACT | 10055 |
| rs186765781 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210487 | ATATGCCCCAAGTGC[C/T]ACAGCCGCTACGGGT | 10055 |
| rs186801096 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | SAE1 | GRCh38.p7 | 19:47185867 | TCAGCCTCCCAAAGT[G/T]CTGGGATTACAGGCA | 10055 |
| rs186823212 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47207018 | AATGTTCCCTTGACT[G/T]GGTGCAGTAGCTCAT | 10055 |
| rs186829102 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47145014 | GTTTTGTTTTGTTTT[G/T]TTTTTGAGACGGAGT | 10055 |
| rs186832221 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | SAE1 | GRCh38.p7 | 19:47164394 | GGATGGTCTCCATCT[C/G]CTGACCTCGTGATCC | 10055 |
| rs186837012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47169120 | ACCATTCCTCTGCCA[A/G]GAAACATTTAATTTT | 10055 |
| rs186837995 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47206820 | CTAAGAATTTACTAC[C/G]TGCTCGGCACTTTAC | 10055 |
| rs186963237 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47154181 | CTGCAACCTCCACCT[A/C]CTGGATTCAAGTGGT | 10055 |
| rs186974722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47175620 | GCACATGCCTGTAGT[C/T]CCAGCTACTTGGGAG | 10055 |
| rs186982222 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182270 | GCAAAGCAGGCCATA[G/T]GCAGCCATCGCTATT | 10055 |
| rs186982711 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47194043 | CTTCTTGGAACACTT[C/T]ATAACCCATTTCTGA | 10055 |
| rs186998283 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47189084 | CACAGTCATTGCTCA[G/T]TGTATATTTATTGAA | 10055 |
| rs187016562 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47135301 | TATTTTTGTATCCAT[C/T]AGTCATCCCTCCTTC | 10055 |
| rs187163380 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47156410 | CTTGAACTGGGGAGG[C/T]GGATGTTGCAGTGAG | 10055 |
| rs187178694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47198068 | AACAGGCTTAGGATT[C/T]GATTGGAGAAGACCA | 10055 |
| rs187202694 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SAE1 | GRCh38.p7 | 19:47139152 | AGATGGAGTTTCACC[A/G]TATTGGCCAGGCTGG | 10055 |
| rs187247923 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SAE1 | GRCh38.p7 | 19:47194656 | TTCCTTGGGCAGTAT[A/G]TAGGGAACAAGAATG | 10055 |
| rs187278765 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47176442 | TGATTTTGTTTCACT[A/G]TTGCCTAATGGCGCA | 10055 |
| rs187317651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47144615 | GAGGCAAGAGAATGG[C/T]GTGAACCTGGGAGGC | 10055 |
| rs187368060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47149358 | GTATTTTTAGTAGAG[A/G]TGGCATTTCACCATG | 10055 |
| rs187372771 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47172327 | AAAATGCCTCCTCTT[A/G]ATAGTGGGATCAGGT | 10055 |
| rs187373548 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47179185 | CGACAGAACAAGGCT[C/T]TGTCTCCAAAAAAAA | 10055 |
| rs187404382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47132508 | AGCGATCCTCGGCCT[C/T]AAGAGATCTCCCCCC | 10055 |
| rs187419710 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SAE1 | GRCh38.p7 | 19:47180047 | GGTATTGGATTGGAA[C/T]TGAAGTTATCTGGAT | 10055 |
| rs187510995 | snp | A/G | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190158 | CAGCATCCTGAGTTA[A/G]TTAAAAGGTGCAGAT | 10055 |
| rs187594805 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47163894 | CTGGCCTCAGCCTCC[C/G]GAGTAGCTGGGATTA | 10055 |
| rs187596144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47137653 | AGGCGTATGCCATAT[C/T]ACTCAGCTAATTTTG | 10055 |
| rs187613302 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176809 | CTTGAGAGTTGGCCT[C/T]GCCATCTGTGAGCAA | 10055 |
| rs187704050 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47173135 | CTGGGTTCGAGCGAT[A/T]CTACAGGCACGCACC | 10055 |
| rs187713943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190994 | GTTTCTTTTGGATTC[C/T]ATTAGGGTTAAGAAG | 10055 |
| rs187751776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47172015 | ACCTCCACCTCCCGG[C/T]TCAAACAGTTTCCCC | 10055 |
| rs187879620 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47155425 | GATTTTTCAAGACAA[C/T]GAGAAATGCAAACTT | 10055 |
| rs187886808 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47207765 | TCAGCTTCCTGAGGC[A/C]CTGAGACTATAAGCA | 10055 |
| rs187911220 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47164977 | TTTTTAGTAGAGACG[G/T]AGTTTCACCATATTG | 10055 |
| rs187981874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47143777 | GGGTTTGAATTCTAG[C/T]TCCACCACATCTAGC | 10055 |
| rs187987869 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47161857 | TCTTAAAAATTGGTT[G/T]TATATTGTATGCATG | 10055 |
| rs187998583 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47204958 | GAAGCATCTTATACA[A/G]GGTCACATAACCAGT | 10055 |
| rs188046204 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SAE1 | GRCh38.p7 | 19:47196726 | TTTCTGCCCCCTTCA[A/G]ACTCATATATACTTC | 10055 |
| rs188098693 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47148814 | AGATGGGGTTTCACC[A/C]TGTTGGTCAGGCTGG | 10055 |
| rs188200465 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47186259 | ATAAAAATAAAAAAA[A/T]AATAATAAAAGCTCA | 10055 |
| rs188237067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47145560 | CTCTCTACATTCCCA[C/T]GCCTCAGTGACATTT | 10055 |
| rs188257782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47154776 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCACCC | 10055 |
| rs188326198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47146737 | CCCAGGCATCTGACT[C/T]CAGAGCCCATGTTCT | 10055 |
| rs188340239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47166583 | CTCCGTTTCATCATA[C/T]AGTAGCCTAACATAT | 10055 |
| rs188343952 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209400 | CGAAGGAGGTGGTGC[C/T]GACGTGCTGCTTCCC | 10055 |
| rs188347979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47187307 | TAGCCCTCAGATGCA[A/G]CGGTGAAAGTGGGAC | 10055 |
| rs188382265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47131445 | GTGCTGCACACAGGG[A/G]AGACTGGACTGGCCA | 10055 |
| rs188406447 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SAE1 | GRCh38.p7 | 19:47141121 | ATTCTCCTGCCTCAC[C/T]GTCCCGAGTAACTGG | 10055 |
| rs188542599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47136935 | TTCTAGGTGGGATAG[A/G]AGAACTCTGGAGACT | 10055 |
| rs188580446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47177452 | TAGCCTTGAACTCCT[A/G]GGCTCAAGTTATCCT | 10055 |
| rs188590656 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47197636 | AGATCTGTAAACATT[A/G]TTCTCTACCTTTTTT | 10055 |
| rs188611024 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SAE1 | GRCh38.p7 | 19:47138246 | ACCAGGTTTCGCCAT[A/G]TTGGCCAGGGTGGTC | 10055 |
| rs188625440 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47155696 | ATCCACCCGCCTCAG[A/C]CTCCCAAAGTGCTGG | 10055 |
| rs188678261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190809 | GTTTTATATGACCAC[A/G]GTCTCCACTTCTCAC | 10055 |
| rs188691602 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SAE1 | GRCh38.p7 | 19:47202160 | AAATTTGTCTTAAGG[A/G]ATTATTTCGACGCCT | 10055 |
| rs188694580 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47157878 | CTTGCCTTTGTGCAG[C/G]CTCACCAAGGGCCCT | 10055 |
| rs188742635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47157992 | GCCCTGTGATTTCAA[A/G]GTTCTCTTCCAACAC | 10055 |
| rs188837327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47145996 | CTGAGGTTGTGGTAC[A/G]TGAAAGATTTCCTGG | 10055 |
| rs188915591 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47197696 | GACATCTCCAGATCA[C/G]TACATAGTTTGCTCC | 10055 |
| rs188981566 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47180814 | GGAGCAAGACTTTGT[C/G]TCCCCCGAAAAAGAA | 10055 |
| rs189004138 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191679 | GACACAAGCACCAAC[A/T]GTCACAAGGGACCAA | 10055 |
| rs189015297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47141626 | TTTTGAGGAAATGGC[A/G]TTGGAGTTGGGTTTT | 10055 |
| rs189032134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47151652 | ATGGGCTTGGAAGGA[C/T]GGATCATCTGTGCAT | 10055 |
| rs189220060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47174628 | CCCAGCCTGGAGTGC[A/G]GTGGCATGATCTCAG | 10055 |
| rs189225786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47203482 | CAAAGGTCTTTTCCA[A/G]CCACTTATGAATCCC | 10055 |
| rs189228400 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SAE1 | GRCh38.p7 | 19:47192260 | TGTTGTTGTCGTCGT[C/T]GTTGTTTTGAGACAG | 10055 |
| rs189257459 | snp | G/T | 0.0475351 | 0.146656 | intron-variant | SAE1 | GRCh38.p7 | 19:47133870 | TTTTTTTGTTTGTTT[G/T]TTTTTTTTTTGAGAC | 10055 |
| rs189257671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47152067 | CTGTGAGTGTTATTT[C/T]GGTATTCAGGCTGCT | 10055 |
| rs189259949 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47150622 | GCTGGCTTCTTCTCT[A/G]GGCATATGTTCCCTC | 10055 |
| rs189269613 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47143365 | CTATCTCAGCCTCCT[A/G]AAGTGCTGGGATTAC | 10055 |
| rs189311707 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47133213 | GTGTGGGAGTAACAT[C/G]ATCTGTTTTTTGTTT | 10055 |
| rs189326702 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47174460 | GGAGTGCAATGGTGC[A/G]ATCTCGGTTCACCAC | 10055 |
| rs189487680 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47167443 | GACGGAGTTTCGCCA[C/T]GTTAGCCAGGATGGT | 10055 |
| rs189645634 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209662 | CTTCTTGGACTTATT[C/T]CCCACCTGATACCTT | 10055 |
| rs189758910 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47147501 | CTTGTCGCCCAGGCC[A/G]GAGTGCAGTGGTGAG | 10055 |
| rs189858144 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47187026 | TAGGGGTGGAGGGGG[C/G]GTGCTCAGGAAGTGA | 10055 |
| rs189863283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47156223 | CTGCAGTGAGCCATG[A/G]TCACACCACTGCACC | 10055 |
| rs189908359 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47139172 | GGCCAGGCTGGTCTC[A/C/G]AACTCCTGACCTCAA | 10055 |
| rs189922536 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47188656 | TTGGTTCATTTAATC[C/T]TTAAACCCCACAAGT | 10055 |
| rs189973906 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47171264 | AGGTGTGAGCCACCG[C/T]GCCTGGCAAACCTGG | 10055 |
| rs189982451 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47189422 | ATAAATGAGCCGGGC[A/G]TAGTGGTGCGTGCCT | 10055 |
| rs190003021 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47143029 | ATTTGTTGAATGAAT[G/T]GTTTTGTGCAGTATG | 10055 |
| rs190029861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47140744 | AGGCTGCAGCGAGCC[C/T]TGATCTTGCCACTGC | 10055 |
| rs190067417 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47208501 | GCTGGAGTGCGGTGG[C/T]GCAATCTCAGTTTAC | 10055 |
| rs190073970 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47178307 | ACCGTTGAAAAATGC[A/G]GAGTGCCTGCTTGTA | 10055 |
| rs190110972 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47138689 | GGCAGTAAACATATA[A/T]ACAAGTAGTGTAGCT | 10055 |
| rs190154902 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SAE1 | GRCh38.p7 | 19:47199942 | ATGATGGCTTTTTTT[C/T]TTTTTGGAGACAGAG | 10055 |
| rs190172898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47182316 | CCAGTGGGTTTTTGG[C/T]GTCCAGTAATGACAA | 10055 |
| rs190186155 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47157420 | TAAATCACACCCTCT[C/T]ACAAGTGTGACACTT | 10055 |
| rs190194340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47179685 | AAGTAGCTGGGATTA[C/T]AGGCAAGTAGCAGGG | 10055 |
| rs190289525 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47160757 | GATGGTCTCAATCTC[C/T]TGACCTTGTGATCCA | 10055 |
| rs190311945 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SAE1 | GRCh38.p7 | 19:47204343 | GCTGGGACTACAGGC[A/G]CCTGCCACCACGCCC | 10055 |
| rs190357379 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47132705 | TAGCCTGGGTAATGT[A/T]GCCAAACCCAGTCTC | 10055 |
| rs190413145 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | SAE1 | GRCh38.p7 | 19:47160475 | TCTCAGCTCACTGCA[A/T]GCTCCACCTCCTGGG | 10055 |
| rs190448992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47189169 | GGATAAGAGGTAGTA[C/T]TACCATACTTTGCAA | 10055 |
| rs190466434 | snp | A/T | 0.0115144 | 0.0749975 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47128823 | TTTATTTATTTATTT[A/T]TTTATTTTTTTCTGA | 10055 |
| rs190483912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47147832 | GGCGCGATCTTGGCT[C/T]ACTGCAAGCTCTGCC | 10055 |
| rs190489757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47169187 | TATTGTTAGACTTAC[A/G]TTCTTGCCCCTCATT | 10055 |
| rs190551605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47183513 | CTTCACAGGCACCTC[A/G]TGACATTTTCTTATT | 10055 |
| rs190589896 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | SAE1 | GRCh38.p7 | 19:47153793 | GCATATTATTATTAT[G/T]ATTATTTTATTTTTT | 10055 |
| rs190603129 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SAE1 | GRCh38.p7 | 19:47193371 | TGGCCAATTGTTACA[A/G]CTTTGAGTTGACTGC | 10055 |
| rs190624178 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47154286 | AGCAGAGACGGGGTT[G/T]CACTATGTTGGCTAT | 10055 |
| rs190634403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47175724 | CCTGGGCAACAGAAC[A/G]AGACTCTGTCTCAAA | 10055 |
| rs190644721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47194187 | GCCATTGGACCTTTA[A/G]CACCCAGGTCTGTCT | 10055 |
| rs190667307 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47135816 | TTTTTTTTTTTGAAA[C/T]GGAGTCTCGCCGTGT | 10055 |
| rs190847017 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SAE1 | GRCh38.p7 | 19:47175507 | ATTGTGAGGCTGAGG[C/T]GGGCAGATCATTTGA | 10055 |
| rs190876606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47134675 | GGGTTTGCGGCAGCA[A/G]ATAGCTTTGTTTGAA | 10055 |
| rs190940654 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47179336 | CATGGTGAAACCCTG[C/T]CTCTACTAAAGTACA | 10055 |
| rs190949581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47148361 | ATGGTTGGTAGGAGG[C/T]GTTGAGGGGAGATTA | 10055 |
| rs191112415 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | SAE1 | GRCh38.p7 | 19:47174838 | TCAGCCTCCCAAAGT[G/T]CTGGGATTACAGGCG | 10055 |
| rs191116331 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | SAE1 | GRCh38.p7 | 19:47144647 | GAGCTTGCAACGAGC[C/G]GAGATCATGCCACTG | 10055 |
| rs191119876 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SAE1 | GRCh38.p7 | 19:47192833 | GTGTGAGCCACTGCA[C/T]CTGGCCTCCTTTATT | 10055 |
| rs191125987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47164090 | TGTGTATATATATGT[A/G]CATGGTTTTGTCTTT | 10055 |
| rs191181633 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | SAE1 | GRCh38.p7 | 19:47156464 | AGCCTGGCGACAGAA[C/T]GAGACTCTGTCTCCA | 10055 |
| rs191185562 | snp | A/C | 0.00199481 | 0.0315187 | utr-variant-5-prime, upstream-variant-2KB, synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47130843 | CAGAAGCACTCCGGG[A/C]GTGCTGCCGGCGGCG | 10055 |
| rs191198797 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47198855 | CTTTGGGAGGTTGAG[G/T]CAGGCAGATTGCTTT | 10055 |
| rs191242274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47145296 | GTGAGCCACCGCACC[C/T]GGCCATGCCTGGCTA | 10055 |
| rs191385993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47207462 | CAGCTTGCCTAGGTG[A/G]TGTCTTCCTCTTTAA | 10055 |
| rs191395779 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47157904 | GCCCTGCGGACCGAC[A/T]GGGCTGGACTGGGTT | 10055 |
| rs191405346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47164749 | TGCCTCCCAGGTTCA[A/G]GCGATTCTCCTGCCT | 10055 |
| rs191411380 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SAE1 | GRCh38.p7 | 19:47185988 | CTCATGCCTGTAATC[C/G]CAGCACTTTGGGAGG | 10055 |
| rs191413390 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SAE1 | GRCh38.p7 | 19:47138026 | GAGCCACTACACCCG[A/G]CCTATGTGTGTGTAT | 10055 |
| rs191486105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190282 | GTGTTTGATCTTAAC[A/G]GAACAGTTTTATAAT | 10055 |
| rs191549387 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47201558 | TGTATTTTTAGTAGA[C/G]ACGGGGTTTCACCAT | 10055 |
| rs191561124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47141693 | AATGGTGCATTTTGC[A/G]AGGGTGGAATGTTGT | 10055 |
| rs191565372 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47158083 | TTGTGCTCAGAGAGT[G/T]CAGGGTGGGGGTGGG | 10055 |
| rs191627204 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47141158 | AGGCGCCTGCCACCA[C/T]GCCTGGCTAATTTTT | 10055 |
| rs191653223 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47180383 | TCAAAAGAACAAGAA[G/T]AATAATCAATTAATG | 10055 |
| rs191664748 | snp | C/T | | | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210700 | CCTCTGTTCCTCAAC[C/T]CTGCATCACCTGCTC | 10055 |
| rs191747838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47144296 | CTGAGATGGCACCAC[C/T]GCACTCCAGCCTGGG | 10055 |
| rs191759712 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | SAE1 | GRCh38.p7 | 19:47185413 | AGGTTCAAGTGATTT[G/T]CCTGCCTCAGCTTCC | 10055 |
| rs191789371 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SAE1 | GRCh38.p7 | 19:47202538 | TGATCCGCCCACCTC[A/G]ACCTCCCAAAGTGCT | 10055 |
| rs191809738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47182132 | ATTCTTCAATTTCCC[C/T]TCATTCACACTCCCA | 10055 |
| rs191840167 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SAE1 | GRCh38.p7 | 19:47142324 | GGGAGGCGGAGGTTG[C/T]AGTGAGCTGAGATCA | 10055 |
| rs191843031 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47158656 | GCTGTGGCTGCCCTC[A/C]CTGCCGCAGCCAGCT | 10055 |
| rs191898371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47134456 | TGGGAGGGTTGAAGG[C/T]ACCTGGAATAGATTG | 10055 |
| rs191904994 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47132565 | TACAGGCATGAGCTA[C/T]CATGCCTGGCCTCAT | 10055 |
| rs191999727 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47205304 | ATTTGTTAGTCACAC[C/T]GTTTTCCTAAGGCTA | 10055 |
| rs192034306 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47206846 | TTTACAAGCCTAGTC[A/T]CATTTCATTCTCACC | 10055 |
| rs192056192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47163764 | TATATGGGAGGATGC[A/G]CGTAGAGTATATGCA | 10055 |
| rs192069880 | snp | C/T | 3.31631e-05 | 0.00407191 | synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150219 | AACTCCAGAAGATCC[C/T]GGAGCTCAGTTCTTG | 10055 |
| rs192080435 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47172908 | TGCTATTAACACCAC[C/G]AGCTACAGAGGGGAA | 10055 |
| rs192090848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190857 | TGAAATTAACAGAGG[C/T]GAGGCCCATCTGGAA | 10055 |
| rs192209308 | snp | C/G | 0.00470027 | 0.0482498 | intron-variant | SAE1 | GRCh38.p7 | 19:47152884 | AAACCCAGCCAATTT[C/G]TTTCTTTCTGCAGGT | 10055 |
| rs192275507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47196731 | GCCCCCTTCAAACTC[A/G]TATATACTTCATTGA | 10055 |
| rs192312466 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47155509 | CTTGTCGCTCAGGCT[A/G]GAGTGCAATGGCATG | 10055 |
| rs192349376 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47185615 | CAGCCTATTTTTGTT[C/T]TTTTGAGACAGAGTC | 10055 |
| rs192373131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191500 | AACACTGCCTGAGCA[A/G]ATGGAGGCAAAGCTG | 10055 |
| rs192424227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47180834 | CCGAAAAAGAAGATG[C/T]TTTTAAATGAATTAC | 10055 |
| rs192431375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47151107 | AAAGGCCCCAGTATG[C/T]TACATGAGAGGTTAG | 10055 |
| rs192525996 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47194891 | GGGACTACAGGCGTG[C/T]GCCACCACGCCTGGC | 10055 |
| rs192526228 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47146029 | TCCTGATCTGAGCTA[A/G]GTCTTAAAGAACAAG | 10055 |
| rs192540391 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47187181 | TGCCGTGAATGGTTA[A/G]AGGCCAGGAGAGCCA | 10055 |
| rs192713618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47177322 | CAGCTATAACAGAGG[A/G]CTATAGAAACTATCA | 10055 |
| rs192734275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47172211 | GGCGTGAGCCACCAC[A/G]CTCAGCTGGATGAAC | 10055 |
| rs192750484 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47132013 | GACGTCTTTTGTTTT[A/G]TGCAGTTGGGTGACC | 10055 |
| rs192773373 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47173476 | TGTCCCCTCAGTTCA[A/G]TGACCCCTGTGATGT | 10055 |
| rs192784767 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47202172 | AGGAATTATTTCGAC[A/G]CCTGTGTCTTTGTCA | 10055 |
| rs192787696 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47132915 | AAAAAATCCACAAGC[A/G]TGTGTATATGTGTCA | 10055 |
| rs192878846 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47160522 | GCCTCAGCCTCCCGA[A/G]TAGCTGGGACTACAG | 10055 |
| rs192892655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47203946 | GAGTGCCTGCTCTGT[A/G]CTTAGCTCACAGTTG | 10055 |
| rs192959382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47186571 | GGGTTGAGTCATCCT[A/G]GTCTTTAATTTGGTA | 10055 |
| rs192960037 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47148866 | TGATCTGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 10055 |
| rs192977042 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47145859 | CAACAAGCATCTGAG[A/G]GCACCTACTGGGTGC | 10055 |
| rs193090026 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | SAE1 | GRCh38.p7 | 19:47182464 | AAAAGAAAAAAGCGT[A/T]GTGTGTGTGTGTGTG | 10055 |
| rs193110769 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47208520 | ATCTCAGTTTACTGC[A/C]ACCTCTGCCTCCTGG | 10055 |
| rs193112889 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47136961 | AGACTGGAGTTCCTT[A/T]ATGAAACAGAAGCCC | 10055 |
| rs193116712 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176667 | TGTTTTTTATTGCCC[C/T]ATTCACAATTCAGCC | 10055 |
| rs193180575 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47165297 | GTTTCACCATGTTGG[C/G]CAGGCTGGTCTCGAA | 10055 |
| rs193186407 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47207823 | TTATTTTTTGTAGAT[A/G]TGGGGTTTTGCCATG | 10055 |
| rs193268599 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SAE1 | GRCh38.p7 | 19:47154914 | GCTGCTCTGTTTTTC[C/T]CACAATAATTTCCTG | 10055 |
| rs199521037 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47138168 | CCTGCCTCAGCCTCC[C/T]AAGTAGCTGGGATTA | 10055 |
| rs199801330 | snp | A/G | 0.00217216 | 0.032884 | missense, nc-transcript-variant, utr-variant-5-prime | SAE1 | GRCh38.p7 | 19:47143522 | CGGGTGCTTCTTGTC[A/G]GCTTGAAAGGACTTG | 10055 |
| rs199816948 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47139610 | TTTTTTTTTTTGAGA[C/G]AGAGTCTCACTCTTG | 10055 |
| rs199824018 | snp | C/T | 0.039522 | 0.134904 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129825 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTACA | 10055 |
| rs199887677 | snp | A/G | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191807 | ACACCTGTAATCCCA[A/G]CACTTTGGGAGGCCA | 10055 |
| rs199918350 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47189618 | GAGGAGTCTACGTTC[A/T]GCTGCAGGGAGCCAG | 10055 |
| rs199923835 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137504 | TTGACAATTACAACT[-/A]AAATTTTTTTTTCTC | 10055 |
| rs199954658 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47142385 | CGAGACTCTGTCTTT[A/T]AAAAAAAAAAAAAAA | 10055 |
| rs199991657 | snp | C/T | 0.00191907 | 0.0309168 | intron-variant | SAE1 | GRCh38.p7 | 19:47152877 | AAAACTCAAACCCAG[C/T]CAATTTCTTTCTTTC | 10055 |
| rs200150830 | in-del | -/CC/TGTGTG/TGTGTGTT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182497 | GTGTGTGTGTGTGTG[-/CC/TGTGTG/TGTGTGTT]CGCGCACGCACGCGC | 10055 |
| rs200166377 | in-del | -/G | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47148028 | GCCTCCCAAAGTGCT[-/G]GGATTACAGGCGTGA | 10055 |
| rs200195395 | snp | A/C | 3.29462e-05 | 0.00405857 | missense, nc-transcript-variant, utr-variant-5-prime | SAE1 | GRCh38.p7 | 19:47143541 | TGAAAGGACTTGGGG[A/C]TGAAATTGCCAAGAA | 10055 |
| rs200240904 | in-del | -/ATCCACCC | 0.0185938 | 0.0946107 | intron-variant | SAE1 | GRCh38.p7 | 19:47141381 | TCCTGACCTCAGGTG[-/ATCCACCC]ATCTCAGCCTCCCAA | 10055 |
| rs200284312 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47177997 | CTGTAATCCCAGCAC[-/T]TTTGAGAGACTGAGG | 10055 |
| rs200289595 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47149939 | AAATTAGCTGTTGTG[C/G]TGGTGCGTGCTTGTA | 10055 |
| rs200347438 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47193845 | AAAAAAAAAAAGAAA[A/G]AAAAGAAAAAGAAAA | 10055 |
| rs200452248 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184803 | TTTTGTTTTGTTTTT[G/T]TTTTGTTTTGTTTTG | 10055 |
| rs200468247 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47198115 | CAATCTCTCTCTCTC[-/T]TTTTTTTTTTTGAGA | 10055 |
| rs200503279 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47140153 | GTTCTGTTGCCCAGG[A/G]TGGAATGCAGTGGCG | 10055 |
| rs200629823 | snp | G/T | 0.00199799 | 0.0315437 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47169824 | TTTCCACAGAAGGTG[G/T]TCTTCTGCCCTGTTA | 10055 |
| rs200647712 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47172780 | GCCAAAAAAAAAAAA[C/T]AGAAAAGAAAAAAAG | 10055 |
| rs200694527 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137727 | TGTGTGTGTGTGTGT[G/T]TTGTTTTTTTTTTTT | 10055 |
| rs200766691 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47168192 | TCTGGAAAAAAAAAA[-/A]TGTTTAAAACAAAAA | 10055 |
| rs200780949 | in-del | -/ATT | 0.040671 | 0.13668 | intron-variant | SAE1 | GRCh38.p7 | 19:47138501 | AGATAAATGTTGGCC[-/ATT]ATTATTTTATTATGT | 10055 |
| rs200843658 | in-del | -/AAAAGAAAG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47193837 | TCTCAAAAAAAAAAA[-/AAAAGAAAG]AAAAGAAAAAGAAAA | 10055 |
| rs201028206 | in-del | -/TG | 0.00879807 | 0.0657391 | intron-variant | SAE1 | GRCh38.p7 | 19:47155469 | CCAAACTTTTTTTTT[-/TG]TGTGTGTGTGAGATG | 10055 |
| rs201184459 | snp | A/G | 0.00115249 | 0.0239774 | synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47169856 | AGAAGCCCTGGAGGT[A/G]GACTGGAGCAGTGAG | 10055 |
| rs201192783 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47161198 | TTTTTTTTTTTTTTT[G/T]AGATCTCTTGCTGTG | 10055 |
| rs201254236 | in-del | -/GTG | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47149942 | TTAGCTGTTGTGGTG[-/GTG]CGTGCTTGTAGTCCC | 10055 |
| rs201311883 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47180983 | GAGAATAGAGGAAGG[-/T]TTTTTTTTCTTTTGC | 10055 |
| rs201318034 | in-del | -/TTTTG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184799 | TTGTTTTTGTTTTGT[-/TTTTG]TTTTGTTTTGTTTTG | 10055 |
| rs201475653 | snp | A/G | 0.00169532 | 0.0290652 | intron-variant, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197315 | GTTGTTGCTCCAGAT[A/G]CGAAATGATGTGCTT | 10055 |
| rs201495640 | in-del | -/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47193869 | AAGAAAAAGAAATTA[-/C]CTCTTCTCTGATATG | 10055 |
| rs201512346 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47179502 | ACAGAGCATCTTAAG[-/A]AAAAAAAAAAAAGAA | 10055 |
| rs201521902 | snp | A/G | 6.59163e-05 | 0.00574054 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150257 | CTGGGTCTGTTGGCC[A/G]AAATAGGGCTGAAGC | 10055 |
| rs201525450 | in-del | -/CTACGTTC | | | intron-variant | SAE1 | GRCh38.p7 | 19:47189610 | ACCCTGGGGAGGAGT[-/CTACGTTC]AGCTGCAGGGAGCCA | 10055 |
| rs201543966 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47186251 | TCTCAAAAATAAAAA[A/T]AAAAAAAAAATAATA | 10055 |
| rs201739841 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47186259 | TAAAAATAAAAAAAA[-/T]AATAATAAAAGCTCA | 10055 |
| rs201802562 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47152586 | TAAGTTATTTTTTTT[-/T]ATGAGAACTATGAAA | 10055 |
| rs201895847 | in-del | -/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47181747 | GCCTCCTGAAGTGCT[-/G]GGATTATAAGTGTGA | 10055 |
| rs201935403 | snp | C/T | | | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150272 | GAAATAGGGCTGAAG[C/T]CTCTTTGGAGCGAGC | 10055 |
| rs201964522 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47168338 | CTCTCTCTGTTTTTT[-/T]CTGTCACCCAGGCTG | 10055 |
| rs201971364 | snp | A/C | 0.00199809 | 0.0315445 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47155153 | TAGCCAAGGAGTAGA[A/C]GATGGGCCCGACACC | 10055 |
| rs202068723 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47140624 | AAAAAAAAAAAAAAA[-/A]CCCATAAATCAGCCA | 10055 |
| rs202087338 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47131697 | GTAGCTTAGGGAATT[C/T]TTTTTTTTTTTTTTT | 10055 |
| rs202103677 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47146296 | TTCAAATGACAGGAA[C/G]GGTGACATGGTTAGC | 10055 |
| rs202128067 | in-del | -/AG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47154458 | TAAGCTGCCCACAGC[-/AG]AGGGGCAGAATTAAG | 10055 |
| rs202158987 | in-del | -/AG | 0.0425829 | 0.139564 | intron-variant | SAE1 | GRCh38.p7 | 19:47172779 | CGCCAAAAAAAAAAA[-/AG]AGAAAAGAAAAAAAG | 10055 |
| rs202245801 | in-del | -/TT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47181477 | TGTTTTTTCTTTTCC[-/TT]TTTTTTTTTTTTTTT | 10055 |
| rs367564725 | snp | A/G | 0.000562693 | 0.016764 | intron-variant, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47180286 | GCTGTTTCCAGATCT[A/G]GGGTAGGAAAATTAC | 10055 |
| rs367585631 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47168571 | AGTGCTGAGATTACA[A/G]AAGTGAGCCACCACA | 10055 |
| rs367601315 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47133837 | AAGAGTCAGTTCTCT[C/T]TTAGGTTTCAGATTT | 10055 |
| rs367624193 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47161041 | GGATGTAACTCTGTA[G/T]CCCAGGCTGGAGTGC | 10055 |
| rs367636973 | snp | A/C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47148613 | CTCTCCACCTCTCTG[A/C/G]GTTCTTTTTTTTTTT | 10055 |
| rs367653268 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47131936 | GATCTCCTTACCTCA[A/T]GTGATCCACCCGCCT | 10055 |
| rs367718909 | snp | C/T | 8.23744e-05 | 0.0064172 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47169897 | CTGCTCTGAAGCGCA[C/T]GACCTCCGACTACTT | 10055 |
| rs367829929 | in-del | -/TCTC | | | intron-variant | SAE1 | GRCh38.p7 | 19:47198103 | GTGACTAGGTCACAA[-/TCTC]TCTCTCTCTTTTTTT | 10055 |
| rs367851923 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47180440 | AGTCTATCTTTGACT[A/C]TCACCATAGTAGTAA | 10055 |
| rs367868877 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47207134 | CAAAAGTCCCAGCTA[C/T]TCAAGAGGGTATGGG | 10055 |
| rs367910261 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47157543 | GCCATTCACAGCTGG[-/A]AGTTTCCCTGGAGTC | 10055 |
| rs367977098 | in-del | -/CTCT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47131733 | TTTGAGATAGTCTCT[-/CTCT]GTCGCCCAGGCTGGA | 10055 |
| rs368025299 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47192650 | TGGGTTCAAGCAATT[A/C]TACTGCCTCAGCCTC | 10055 |
| rs368088623 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47197714 | CATAGTTTGCTCCCT[A/C]TTTTCCACAGCTCCT | 10055 |
| rs368105742 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150337 | GACACTGAGGATATA[C/G]AGAAGAAACCAGAGT | 10055 |
| rs368129410 | in-del | -/AAACAA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47144720 | AACAACAACAAAAAC[-/AAACAA]AAACAAACAACACTG | 10055 |
| rs368206294 | in-del | -/A | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191328 | CATCTCAAAAAAAAA[-/A]GAAGAAAAACAAAAA | 10055 |
| rs368282308 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47140533 | ATGGGATTTGTAAAC[A/C]CAGCACTTTGAGGGA | 10055 |
| rs368351235 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47207253 | AATTAAAAACATTTA[C/T]AAATAAATAAAATTT | 10055 |
| rs368370800 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47132771 | CATAAGTTTATAGTC[C/T]CAGCTTGTCAGGAGA | 10055 |
| rs368388364 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | SAE1 | GRCh38.p7 | 19:47152852 | ATCAGGGCAGTGATT[C/T]ACAGTTTGCAAAACT | 10055 |
| rs368436624 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47148880 | CGGCCTCCCAAAGTG[C/T]TGGGATTACAAGCGT | 10055 |
| rs368449287 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47155630 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 10055 |
| rs368455283 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47192865 | TATGGGACATTTTTT[G/T]AAAAGAGGCTTGGTC | 10055 |
| rs368479044 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47199133 | GGCTCACGCCTGTAA[A/T]CCCAGCACTTTGGGA | 10055 |
| rs368502773 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47202151 | TATATTTAGAAATTT[A/G]TCTTAAGGAATTATT | 10055 |
| rs368506089 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47147774 | GTATTTTTTTTTTTT[C/T]TTGAGACAGAGTCTC | 10055 |
| rs368510819 | snp | C/T | 0.0117023 | 0.0755925 | intron-variant, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47131031 | AGGCCCAGAAACGGT[C/T]AGGGCCGGCGCGGCT | 10055 |
| rs368541771 | in-del | -/AAAA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47181354 | AAATAAAAAACAAAT[-/AAAA]AGGTCTGTAGGTTAG | 10055 |
| rs368543363 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47171495 | GAGTCTCACTCTGTT[C/G]CCCAGGAGAGCAGTG | 10055 |
| rs368587435 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | SAE1 | GRCh38.p7 | 19:47152878 | AAACTCAAACCCAGC[C/T]AATTTCTTTCTTTCT | 10055 |
| rs368727724 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47179739 | CCAGCTGATTTTGGT[A/G]TTATTTGTAGAGACG | 10055 |
| rs368789052 | snp | A/G | 0.00116962 | 0.0241545 | intron-variant | SAE1 | GRCh38.p7 | 19:47169780 | TGATTGGAAGCCAGC[A/G]TATGTTATTCCTAAG | 10055 |
| rs368853479 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47138080 | CGGAATTTCTCTCTT[C/G]TTGCCCAGGCTGGAG | 10055 |
| rs368881851 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47204797 | CACCGCACCCGGCCA[A/G]GCCCCCGTCTTTTTA | 10055 |
| rs368887138 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | SAE1 | GRCh38.p7 | 19:47203795 | CTTTGTATATGTGCT[A/G]ACAGAGAGAATGGAA | 10055 |
| rs368916335 | in-del | -/AA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47196368 | TTTTTTTTTTTTTTT[-/AA]TTTTACTTTTTTGAG | 10055 |
| rs369007842 | snp | C/G/T | 0.000379112 | 0.0137629 | intron-variant | SAE1 | GRCh38.p7 | 19:47143480 | TCATCAGGTTAACAA[C/G/T]GTTTGTCTTACAGGC | 10055 |
| rs369016483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47188724 | TCCTTGTCACTTGCC[C/T]AAGGTCACAGTAAGT | 10055 |
| rs369113659 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SAE1 | GRCh38.p7 | 19:47141660 | GGGGAAAGGCGTAGG[C/T]AGGCATTGAGAGGAA | 10055 |
| rs369125953 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47151150 | GTAGTTTTTTTTTTT[-/T]GCACCTTTTTTTATT | 10055 |
| rs369144271 | in-del | -/AC | | | intron-variant | SAE1 | GRCh38.p7 | 19:47196374 | TTTTTTTTTAATTTT[-/AC]TTTTTTGAGACGGAG | 10055 |
| rs369154318 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47165989 | CCTGGTTGGGGTCCT[G/T]TGCCCACTTCTGGCT | 10055 |
| rs369209902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47181043 | AAAAGAGGCCCCGGC[A/G]TGGTGGCTCACGCCT | 10055 |
| rs369223748 | snp | A/G | 8.23798e-05 | 0.00641741 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47143594 | GGACTGACCATGCTG[A/G]ATCACGAACAGGTGC | 10055 |
| rs369243081 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47174173 | TAATATATCCTATCA[C/T]GTTTACCACTCTCTC | 10055 |
| rs369250353 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129277 | TCTACTAAAAATACA[A/G]AAGTTAGGTGGGCAT | 10055 |
| rs369251904 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | SAE1 | GRCh38.p7 | 19:47201883 | AATGATCCACCCGCC[G/T]TGGCCTCCCAAAGTG | 10055 |
| rs369270925 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47205342 | TTTTTTTTTTTGTCT[A/T]TTTTTTCTGATCCTT | 10055 |
| rs369284296 | snp | A/T | 0.000148262 | 0.00860865 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47143588 | GTGAAAGGACTGACC[A/T]TGCTGGATCACGAAC | 10055 |
| rs369386001 | snp | C/T | 4.97253e-05 | 0.004986 | intron-variant | SAE1 | GRCh38.p7 | 19:47155255 | AGAAACCCTGGGGCC[C/T]TGGAGGGGTCAGGCA | 10055 |
| rs369409631 | snp | C/T | 0.0248432 | 0.108648 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129808 | CCTCCTTCCTTCCTT[C/T]CTTTCTTTCTTTCTT | 10055 |
| rs369464890 | in-del | -/AGTGGCTCACGCCTGTAACCCCAGCGC | | | intron-variant | SAE1 | GRCh38.p7 | 19:47189286 | CTGGGGGCTGGGCGC[-/AGTGGCTCACGCCTGTAACCCCAGCGC]TTTGGGAGGCTGAGG | 10055 |
| rs369489733 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47133047 | CCTGTGGTCATCTGG[C/G]AGAACTTTCCTAGCT | 10055 |
| rs369514280 | in-del | -/CT | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191635 | CTGTGCTAGATGACT[-/CT]TGTGCGATCTTATTT | 10055 |
| rs369574114 | snp | A/G | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47153030 | AATCTAGGAGAGCAT[A/G]AGTTTGTAGAGTAAG | 10055 |
| rs369593722 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47160458 | GGAGTGCAGTGGTGC[A/G]ATCTCAGCTCACTGC | 10055 |
| rs369634609 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47139862 | CGCCTTGGCCTCCCA[A/G]AGTGTTGGGATTATA | 10055 |
| rs369645255 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47198492 | GAGGCTTCCTAAACT[C/T]GGCTTTGCAGTGCCT | 10055 |
| rs369669231 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47166904 | ACAATGGATTTAACT[A/C]CTAAAGGAAAGCCAC | 10055 |
| rs369693220 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47158461 | CACATGGACACTGAC[A/G]TGCAGGAGCCAGAGG | 10055 |
| rs369694869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47150963 | CTGCCAAATCTATGC[A/G]GAGGTGAAAGGATAA | 10055 |
| rs369768067 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47204509 | AGCCGCACCCCCCCC[C/T]TTTTTTTTTTTTTTT | 10055 |
| rs369785309 | in-del | -/GCCACCTCTTTTTGTAAATAAAGTTT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47200708 | TTGGCAAACTGGCTT[-/GCCACCTCTTTTTGTAAATAAAGTTT]TATTGGCACACTTAC | 10055 |
| rs369850909 | snp | G/T | 1.65436e-05 | 0.00287602 | intron-variant | SAE1 | GRCh38.p7 | 19:47155069 | TGATTCCAATAACAT[G/T]ATTCCTAGGGTAAAA | 10055 |
| rs369876592 | in-del | -/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47131697 | GTAGCTTAGGGAATT[-/C]TTTTTTTTTTTTTTT | 10055 |
| rs369884147 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47193084 | TTTTTTGGAGACAGA[A/G]TCTTGCTCTGTCGCC | 10055 |
| rs369887508 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47176996 | AACAGCATTCACTTA[A/C]CAGCATGAACAATAA | 10055 |
| rs369947043 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182280 | CCATAGGCAGCCATC[A/G]CTATTTGGGTATGAC | 10055 |
| rs370065807 | in-del | -/GATTTGGGATTCTTA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47186287 | CATTGGAGCATTTTG[-/GATTTGGGATTCTTA]GATTTGGGATTCTTA | 10055 |
| rs370088654 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47202288 | TAAAATTATACCTAT[G/T]TATTTATTTATTTAT | 10055 |
| rs370109515 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47161394 | AAAACAAACACTATC[C/T]GCCTTAAAAACACAA | 10055 |
| rs370109729 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47210039 | ACAGAACCCCAGTCA[C/T]ATGCGGCTCAAGTCA | 10055 |
| rs370111806 | in-del | -/AC | | | intron-variant | SAE1 | GRCh38.p7 | 19:47201602 | AACTATTCCTCCAAT[-/AC]GGCCAAAATGAGATT | 10055 |
| rs370183212 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47168633 | TTGAGACAGAGTTTC[A/G]CTCTTGTTGCTGAGG | 10055 |
| rs370228863 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47145102 | CTGCCTCCCAGGTTC[A/G]AGCAATTCTCCTGCC | 10055 |
| rs370359276 | snp | C/T | 3.29968e-05 | 0.00406169 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150238 | GCTCAGTTCTTGATT[C/T]GTACTGGGTCTGTTG | 10055 |
| rs370378855 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47149651 | AGCATGGATTTTTTT[-/T]GTTGACAGTGAATTT | 10055 |
| rs370417015 | in-del | -/AGTATTTT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47171633 | ATTTTTTGTATTTTT[-/AGTATTTT]TGTATTTTTTTTGTA | 10055 |
| rs370437002 | snp | C/T | 3.29565e-05 | 0.00405921 | intron-variant | SAE1 | GRCh38.p7 | 19:47203646 | GTTCCCAGTGCTCCA[C/T]TTTCCTTGTCTTCCT | 10055 |
| rs370442437 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47154726 | GTCTCAAACCCTTGA[C/T]CTCAGGTGACACGCC | 10055 |
| rs370450477 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184577 | CACCATGCCCATTTA[C/G]TTTTTGTATTTTTAG | 10055 |
| rs370474074 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47146571 | TAGGCACTGTTCTCA[A/G]AGCTGCAGTTGTATT | 10055 |
| rs370500609 | snp | A/G | 1.66001e-05 | 0.00288094 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150370 | TTTTTCACTCAATTC[A/G]ATGCTGTAAGTTTCT | 10055 |
| rs370503512 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47178262 | AAAAAAAAGAAATCT[A/G]TCTATCTATCAGTCA | 10055 |
| rs370662956 | snp | A/T | 0.0314385 | 0.121371 | intron-variant | SAE1 | GRCh38.p7 | 19:47153102 | ATACTTTTTTTTTTT[A/T]AATTATGTATTTATT | 10055 |
| rs370745297 | snp | C/T | 0.000432947 | 0.0147067 | synonymous-codon, nc-transcript-variant, intron-variant | SAE1 | GRCh38.p7 | 19:47130954 | GAAGGAGGAGGCTGG[C/T]GGCGGCATTAGCGAG | 10055 |
| rs370790641 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47150070 | TGACAGAGCAAGACT[A/G]TCTCAAAAAAAAAAA | 10055 |
| rs370799932 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47132587 | TGGCCTCATTGATCA[A/G]TATTTTTACTTAGCC | 10055 |
| rs370803921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47159817 | TCCTGCCTCAGCTTC[C/T]GGAGTAGCTGGAACT | 10055 |
| rs370815368 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47157827 | GGTTACGAGGCATTC[A/G]GTGCATTCCTGCTGA | 10055 |
| rs370841253 | snp | C/T | 4.99696e-05 | 0.00499823 | intron-variant | SAE1 | GRCh38.p7 | 19:47143652 | TCTGGCTCCCCTTTC[C/T]AGCATGAAGATCTGC | 10055 |
| rs370881991 | in-del | -/GTC | | | intron-variant | SAE1 | GRCh38.p7 | 19:47205338 | TTTTTTTTTTTTTTT[-/GTC]TATTTTTTCTGATCC | 10055 |
| rs370935019 | snp | C/G/T | 8.2364e-05 | 0.00641686 | missense, utr-variant-3-prime, synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209209 | CTTCTTCTTCGATGG[C/G/T]ATGAAGGGGAATGGG | 10055 |
| rs371022916 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47168451 | TGGTACCACAGGTGC[A/G]TGCCACTGCACCCAG | 10055 |
| rs371151332 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47138783 | AGCCAGGCAATTGAG[A/G]CTAGCTTGGGCAACT | 10055 |
| rs371194046 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163346 | TGTACAGACTTTTTT[-/T]CTTGTCATTATTCCC | 10055 |
| rs371221556 | in-del | -/A | 0.429388 | 0.174127 | intron-variant | SAE1 | GRCh38.p7 | 19:47142385 | CGAGACTCTGTCTTT[-/A]AAAAAAAAAAAAAAA | 10055 |
| rs371247946 | snp | A/G | 0.000433604 | 0.0147178 | synonymous-codon, nc-transcript-variant, intron-variant | SAE1 | GRCh38.p7 | 19:47130942 | CGCCATGGTGGAGAA[A/G]GAGGAGGCTGGCGGC | 10055 |
| rs371257672 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137454 | AGATTTGGTTGCTTA[A/C]ATTGAGGCCAAGTTT | 10055 |
| rs371263245 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47185957 | AAAAAATGCTTATTG[A/G]CCCCGGGCGTGGTGG | 10055 |
| rs371314643 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47204979 | CATAACCAGTAACTA[A/G]CACAGCCTTTTGAGG | 10055 |
| rs371452872 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47204603 | CCTCCGCCTCCTGGG[G/T]TCAAGCGATTCTCCT | 10055 |
| rs371497281 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47179848 | GGTGTGAGCCACTTT[A/G]CCTGGCCTAGTAGGT | 10055 |
| rs371526649 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167384 | AGCTGGGACTGCAGG[C/T]GCCTGCCACCACGCC | 10055 |
| rs371540590 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47139261 | GTTAGCCACGATGGT[C/T]TCCATCTCCTGAACT | 10055 |
| rs371597052 | snp | C/G | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176543 | TGTAGAGGGAGAGTA[C/G]TGTGCCCACTGGAGT | 10055 |
| rs371706724 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47133335 | GGTTCAAGCGATTCT[C/T]CTGCCTCACCTTCCT | 10055 |
| rs371707526 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47169914 | ACCTCCGACTACTTT[C/G]TCCTTCAAGGTGAGG | 10055 |
| rs371716900 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47192544 | CAGCCACCATGCCCG[A/G]CTACTTAATTTATTT | 10055 |
| rs371739496 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47181083 | GCACTTTGGGAAGCC[A/G]AGGCAGGTGGATCAC | 10055 |
| rs371753044 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47134414 | TTGATGGGGTGGGGG[A/G]ATGTCATCATGAGGC | 10055 |
| rs371786759 | snp | C/T | 0.000165939 | 0.00910726 | intron-variant | SAE1 | GRCh38.p7 | 19:47152868 | ACAGTTTGCAAAACT[C/T]AAACCCAGCCAATTT | 10055 |
| rs371801413 | snp | A/C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47180377 | GGCATGTCAAAAGAA[A/C/G]AAGAAGAATAATCAA | 10055 |
| rs371815095 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47198273 | TGCCACCACGCCCAG[C/G]TAATTTTTTTTGTAT | 10055 |
| rs371828536 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47133862 | AGATTTGTTTTTTTT[G/T]TTTGTTTTTTTTTTT | 10055 |
| rs371832123 | in-del | -/TT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47194297 | AAAACTATTTGGTCT[-/TT]AAAAAGTGTGACTCT | 10055 |
| rs371839495 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47186261 | AAAAATAAAAAAAAA[-/A]TAATAAAAGCTCATT | 10055 |
| rs371839813 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47140562 | GAGGCAGAGGCAGGA[A/G]GATTGCTTGAGCCCA | 10055 |
| rs371846940 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | SAE1 | GRCh38.p7 | 19:47170598 | TGTAGCCTCTACTTC[C/T]TGGGCTTAAGTGCTC | 10055 |
| rs371894720 | in-del | -/TTAC | | | intron-variant | SAE1 | GRCh38.p7 | 19:47196372 | TTTTTTTTTTTAATT[-/TTAC]TTTTTTGAGACGGAG | 10055 |
| rs371918182 | in-del | -/GTGT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182465 | AAAGAAAAAAGCGTA[-/GTGT]GTGTGTGTGTGTGTG | 10055 |
| rs371997312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47202997 | ACTTGTCTGTGTTCC[A/G]GTTTGCTTGGTGAGC | 10055 |
| rs371999796 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SAE1 | GRCh38.p7 | 19:47156707 | TATTTTTAGTAGAGA[C/T]GGGGTTCCACCATGT | 10055 |
| rs372004271 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47186347 | TGCAAATATTTCAAA[A/G]TCTGAAAATACCCAA | 10055 |
| rs372010344 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47165395 | GCACCCGGCCTTGTT[A/G]TTAGTCTTAACTAGA | 10055 |
| rs372012536 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47142212 | AACATGGTGAAACTC[C/T]GTCTGTACCAAAAAT | 10055 |
| rs372085831 | in-del | -/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47205338 | TTTTTTTTTTTTTTT[-/G]TCTATTTTTTCTGAT | 10055 |
| rs372113235 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47161823 | CAACACATAGAATTG[C/T]TTTGCATGCTTTTTA | 10055 |
| rs372179818 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47134329 | GGGTGGGAGCTTTCA[C/G]AAGGTTTTAGAGGGT | 10055 |
| rs372190226 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47193007 | GTAGAAGTATTGGGT[A/G]GTAGCAGATCAGTGC | 10055 |
| rs372198980 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47149384 | CCATGTTGGCCAGGT[C/T]GGTCTCAAACTCCTG | 10055 |
| rs372214244 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184028 | TTTAGATTTTTTTTT[-/T]CCTTTTTGTAAATTA | 10055 |
| rs372241014 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47133026 | CAGACTTATATGGGA[A/C]AGAGCCCTGTGGTCA | 10055 |
| rs372259801 | in-del | -/AA | 0.0221141 | 0.102801 | intron-variant | SAE1 | GRCh38.p7 | 19:47163266 | CAAAAAAAAAAAAAG[-/AA]AATTGAAATTATGTT | 10055 |
| rs372312714 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SAE1 | GRCh38.p7 | 19:47141361 | TGGACAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 10055 |
| rs372357457 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47171911 | AAAAAGTATTTTTTT[-/T]AATGTTATTTATGCA | 10055 |
| rs372393679 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47174819 | ACCTCGTGATCCGCC[C/T]GCCTCAGCCTCCCAA | 10055 |
| rs372406837 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47154112 | TTATTATTTTTGAGA[C/T]GGAGTTTTGCTTTTG | 10055 |
| rs372411711 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | SAE1 | GRCh38.p7 | 19:47183637 | GGCCCACATCTCCCC[C/G]ACTCCCCCACCCACT | 10055 |
| rs372420431 | snp | C/T | 3.29468e-05 | 0.00405861 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SAE1 | GRCh38.p7 | 19:47143521 | TCGGGTGCTTCTTGT[C/T]GGCTTGAAAGGACTT | 10055 |
| rs372438502 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47199427 | AAGGCAGCAATAGAG[G/T]GGCAGTGCCTGAGCA | 10055 |
| rs372444941 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47140251 | AGCTGGGACTACAGG[C/T]GCCCGCCACCATGCC | 10055 |
| rs372454951 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47187788 | TGGCCTCTCAAAGTG[C/T]TGGGATTACAGGCGT | 10055 |
| rs372494974 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197298 | TATGAGGAAGATTCT[C/G]AGTTGTTGCTCCAGA | 10055 |
| rs372630851 | snp | A/C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47180009 | TGAATGTGGACAGTG[A/C/G]GAAAGGCTAGAAGGA | 10055 |
| rs372647645 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47149027 | TTGCAATTTTTGTTG[G/T]TTTTTGAGAGAGGGC | 10055 |
| rs372654420 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47195682 | TTCCCTTTCCCTTCC[C/T]CTTCCCCTTCGCTTC | 10055 |
| rs372707074 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47197182 | TGAGCCTCCATCTCC[-/A]AAAAAAAAAAAAAGT | 10055 |
| rs372811945 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SAE1 | GRCh38.p7 | 19:47172354 | AGGTGTGGAAGAGGC[A/G]CCAGCAGTAAGAGCA | 10055 |
| rs372953079 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47198357 | CCTCAGGTGATCCGC[C/G]TACCTTGGCCTCCCA | 10055 |
| rs372964602 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184677 | CAGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 10055 |
| rs372977278 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47194465 | CAATCAACATATACG[A/G]AAGAGATATCAATGA | 10055 |
| rs372982669 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47154757 | CGCCTTGGCCTCCCA[A/C]AGTGCTGGGATTACA | 10055 |
| rs373026156 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | SAE1 | GRCh38.p7 | 19:47203622 | TCCAGATGTCATGGT[C/T]ACAGTTCTGTTCCCA | 10055 |
| rs373039269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47160307 | GCTCACTGCAACCTC[C/T]GCCTCCCGGGTTTAA | 10055 |
| rs373043742 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182800 | ATAGTTACTGGTTAC[A/T]GGCGGGGTGTGGTGG | 10055 |
| rs373059534 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163942 | ACCCGGCTAAGTTTT[G/T]TATTTTAAGTAGAGG | 10055 |
| rs373106312 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47203266 | CATGTTAACACAGGC[A/C]TGCTCCCTGACATTT | 10055 |
| rs373120261 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47155404 | GGGCCCAGTGATTCC[A/G]GATGGGATTTTTCAA | 10055 |
| rs373129523 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47204285 | TCACTGCAAGCTCCA[C/T]CTCCCGGGTTCACGC | 10055 |
| rs373203254 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | SAE1 | GRCh38.p7 | 19:47162590 | ATTCTTGGTCCCTCT[-/A]CCCTCCCCACCCCCT | 10055 |
| rs373216182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47172107 | TATTTTTAGTAGAAA[C/T]GGGGTTTCACCATGT | 10055 |
| rs373330940 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47181460 | TTTTGTTTTGTTTTT[C/G]TTGTTTTTTCTTTTC | 10055 |
| rs373366124 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SAE1 | GRCh38.p7 | 19:47181556 | TCATCTCGGCTCACT[A/G]CAAGCTCCACCTCAT | 10055 |
| rs373420732 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47172425 | AGAAGCTTGTTGCTC[A/G]CTGCCTCGCACATAG | 10055 |
| rs373455292 | snp | A/G | 0.000280045 | 0.0118298 | intron-variant, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197343 | CTTGACTCACTGGGT[A/G]TTAGTCCTGACCTGC | 10055 |
| rs373507515 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47189880 | ATGTAACAAACAGTG[A/G]TTAATAATGTTGCTG | 10055 |
| rs373558502 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167388 | GGGACTGCAGGTGCC[C/T]GCCACCACGCCTGGC | 10055 |
| rs373585392 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47188548 | GTATCGGCTTTTCTA[C/G]GGCGAGTGTGAGCTG | 10055 |
| rs373603519 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47179501 | ACAGAGCATCTTAAG[-/A]AAAAAAAAAAAAAGA | 10055 |
| rs373631599 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47144631 | GTGAACCTGGGAGGC[A/G]GAGCTTGCAACGAGC | 10055 |
| rs373654296 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150306 | GAATCTCAACCCCAT[A/G]GTGGATGTGAAGGTG | 10055 |
| rs373677651 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163984 | TTGTTCGCCAGGCTG[A/G]TCTCGAACTCCTGAC | 10055 |
| rs373681536 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47199581 | CTTCAACTCTGCTGG[A/C]CGGTGATGCAGAGCC | 10055 |
| rs373728879 | in-del | -/G | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130250 | GTAGGGACATGAAAG[-/G]CTGGGCACAGTGGCT | 10055 |
| rs373756791 | snp | A/C | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47143601 | CCATGCTGGATCACG[A/C]ACAGGTGCGCTGTTG | 10055 |
| rs373794198 | in-del | -/C | 0.000797681 | 0.019955 | intron-variant | SAE1 | GRCh38.p7 | 19:47169813 | TTCTGCCTTTTTTCC[-/C]ACAGAAGGTGGTCTT | 10055 |
| rs373798611 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47178775 | TCGTGCATAGCCTGC[A/G]TTTTTCTTTTAAAAT | 10055 |
| rs373841441 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47151398 | TCAGGTAATCCACCT[C/G]CCTCGGCCTCCCAAA | 10055 |
| rs373857818 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209451 | AAGGGGCGCAGGGTG[G/T]CTGTCTTTGTTCCAG | 10055 |
| rs373880137 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47147319 | TCAGGGTATTCTCCC[A/G]CTTAAGCCTCCCAGT | 10055 |
| rs373889913 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47168664 | CTGGAGTGCAATGGC[A/G]CGATCTCAGCTCACT | 10055 |
| rs373997899 | snp | A/C/T | 0.000346194 | 0.0131524 | intron-variant | SAE1 | GRCh38.p7 | 19:47155224 | AAAAGGTATGTGTAA[A/C/T]GTGGGGGCAGAGGTC | 10055 |
| rs374007070 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47175945 | ATTTCTGTTAGATAA[A/G]CATCATAGTAAAAAG | 10055 |
| rs374015231 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47201984 | CTTGATAAGCAGGAA[G/T]ATGTTACCCCTGGAT | 10055 |
| rs374051020 | snp | C/T | 1.65381e-05 | 0.00287555 | intron-variant | SAE1 | GRCh38.p7 | 19:47153067 | GAGAGGAGGGGAGAA[C/T]ATAACATTTTCTCCT | 10055 |
| rs374051160 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47143614 | CGAACAGGTGCGCTG[G/T]TGTGAGCTCATTCCT | 10055 |
| rs374057726 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47177942 | TAGTGGTTTCCCTAT[G/T]GATAGAATATCAGAA | 10055 |
| rs374091224 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47139681 | GCAAGCTACACCTTC[C/T]GGGTTCACACCATTC | 10055 |
| rs374094650 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47169446 | GACGGGGGTTTCACC[A/G]TGTTGGCCAGGCTGG | 10055 |
| rs374094942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47197595 | AGTATCTTATATTCA[C/T]GTGGTTCAAAATTCA | 10055 |
| rs374146775 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47146813 | GAAGATGAGGCTTCT[A/G]GCTTGAGTGACTGGG | 10055 |
| rs374154722 | snp | C/T | 0.000108067 | 0.00734996 | synonymous-codon, nc-transcript-variant, intron-variant | SAE1 | GRCh38.p7 | 19:47130957 | GGAGGAGGCTGGCGG[C/T]GGCATTAGCGAGGAG | 10055 |
| rs374200029 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167012 | GCTGGAGTGTAGTGG[C/T]GTGACCTTGGCTCGC | 10055 |
| rs374235352 | in-del | -/CT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163720 | CGACAGAGCAAGACT[-/CT]ATCTCAAAAATAAAT | 10055 |
| rs374269669 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47161925 | AGGCCATCTGTTTAT[A/T]TGTTGTTCTAGGGCT | 10055 |
| rs374326579 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47140808 | TTCAATAAAACAAAA[C/T]GTAAACATGGTATTT | 10055 |
| rs374334375 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47171378 | GGCACACTGCAACCT[C/G]TGCCTCCCAGGCTCA | 10055 |
| rs374394198 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47138137 | CAACCTCTGCCTCCC[A/G/T]GGTTCAGGCAATTCT | 10055 |
| rs374397052 | snp | A/G | 1.64735e-05 | 0.00286993 | intron-variant, synonymous-codon, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47203684 | AGGTACTGCTTCTCC[A/G]AGATGGCCCCAGTGT | 10055 |
| rs374470646 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | SAE1 | GRCh38.p7 | 19:47150186 | AGACTTAAAAAAATA[C/T]GTGTATTATTCCTAG | 10055 |
| rs374528925 | in-del | -/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47195736 | TTTCCTTTTTTTCTT[-/C]TTTTTTTTTTTTTTT | 10055 |
| rs374546697 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47206910 | TATTTGCCCAGAGAA[A/G]CAAACTTCTTTCTGA | 10055 |
| rs374643814 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47158632 | AAAGACGGACGTAGG[A/G]GCAGAGTTGCTGTGG | 10055 |
| rs374686706 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47204619 | TCAAGCGATTCTCCT[C/G]CCTCAGCCTCCCGAG | 10055 |
| rs374713237 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47148159 | ATTTGAATCAAAGAT[C/T]GAATCCAGCCTGAAT | 10055 |
| rs374723445 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | SAE1 | GRCh38.p7 | 19:47158679 | AGCCAGCTCCTTCCA[A/T]GAGTTGCAGAATGCC | 10055 |
| rs374728868 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47188607 | ACAGACCTGGAAGAT[A/G]CTGCCCCAGGCACTC | 10055 |
| rs374840423 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47186197 | GTGAGCCGAGATCCC[A/G]CCACTGCATTCCAGC | 10055 |
| rs374840864 | in-del | -/TT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47189780 | TTTGTGACAGTGACT[-/TT]ATTTTCTTCCTACTA | 10055 |
| rs374853337 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47134138 | AGTGCTGGGATTACA[A/G]GTGTGAGCCACCATG | 10055 |
| rs374924951 | snp | A/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47152928 | TGCTCCAGGGATGTC[A/T]TAGTTAAAGTTGACC | 10055 |
| rs374944798 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47193877 | GAAATTACCTCTTCT[C/T]TGATATGCAGAGCCC | 10055 |
| rs374974349 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47135365 | GTAACCCTCAGTCTA[C/T]TATCTGCATGAGTTC | 10055 |
| rs374984198 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129518 | CGGGCTGGTCTCGAA[A/C]TCCTGACTTCGTGAT | 10055 |
| rs375102593 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182503 | TGTGTGTGTGCGCGC[A/G]CGCACGCGCGCGCGC | 10055 |
| rs375119446 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47160323 | GCCTCCCGGGTTTAA[A/G]CGATTCTCCTGCGTT | 10055 |
| rs375154291 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47133443 | TGTTAGACAGGATAG[C/T]CTCGATCTCCTGACC | 10055 |
| rs375156924 | in-del | -/CACCCATC | | | intron-variant | SAE1 | GRCh38.p7 | 19:47141384 | TGACCTCAGGTGATC[-/CACCCATC]TCAGCCTCCCAAAGT | 10055 |
| rs375167305 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47192621 | GATTTCGGCTCACCG[C/T]AACCTCTGAATCCTG | 10055 |
| rs375299396 | snp | A/C/G | 1.65214e-05 | 0.0028741 | intron-variant | SAE1 | GRCh38.p7 | 19:47143454 | TGATTCTGCAAGCTC[A/C/G]CTGTTCTGTATCATC | 10055 |
| rs375316853 | snp | A/C/G | 0.000265172 | 0.011512 | intron-variant | SAE1 | GRCh38.p7 | 19:47169951 | AGCACAACTTACCCC[A/C/G]GGAGAGCTTTTGGCT | 10055 |
| rs375339052 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47156791 | AGGGGCTCAGCCTCT[A/G]TTTGGATTAGGTGCA | 10055 |
| rs375355795 | snp | A/G | 0.000101031 | 0.00710669 | intron-variant | SAE1 | GRCh38.p7 | 19:47150405 | ATAAAATCTGCTGTG[A/G]GAATTAAACAAATTA | 10055 |
| rs375364401 | in-del | C/TCTTT | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129804 | CCTCCCTCCTTCCTT[C/TCTTT]CTTTCTTTCTTTCTT | 10055 |
| rs375506182 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47169726 | CAGTAAACTTTAAAT[A/G]ATGAGATTTTTCTGC | 10055 |
| rs375509936 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163855 | CAGTGGCGTGATCTC[C/T]GTCTCCCAGGTTCAA | 10055 |
| rs375600677 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47179672 | ATCACAGCCTCCCAA[A/G]TAGCTGGGATTATAG | 10055 |
| rs375709871 | snp | C/T | 8.24219e-05 | 0.00641905 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150248 | TGATTCGTACTGGGT[C/T]TGTTGGCCGAAATAG | 10055 |
| rs375765649 | in-del | -/TAT | 0.00636936 | 0.0560724 | intron-variant | SAE1 | GRCh38.p7 | 19:47153780 | CTAGTTCTTTGGGCA[-/TAT]TATTATTATTATTAT | 10055 |
| rs375823492 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47199648 | TGGCTGCACACTCAC[A/G]GCCCAGCACACAGCC | 10055 |
| rs375844775 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47141511 | AGGTCGTGGAGAGCA[A/G]ATTTATTGTCAGGGA | 10055 |
| rs375845313 | snp | A/C | 0.0337553 | 0.125452 | intron-variant | SAE1 | GRCh38.p7 | 19:47203428 | ACTTATAAAGGTAAA[A/C]ATAAAAGTATTGTGA | 10055 |
| rs375876797 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47178792 | TTTTCTTTTAAAATG[G/T]GTTAAGCACTGTATT | 10055 |
| rs375884120 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47165764 | ATTGTTATGAGTTAG[A/T]TTGAACCAAAAGGAT | 10055 |
| rs375920163 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47154509 | TTTTTTTTTTTTTTT[G/T]TCTGAGACAGACTTT | 10055 |
| rs375977227 | snp | G/T | 6.59337e-05 | 0.0057413 | intron-variant | SAE1 | GRCh38.p7 | 19:47153047 | GTTTGTAGAGTAAGT[G/T]TTGGGAGAGGAGGGG | 10055 |
| rs376048834 | snp | A/C | 3.2962e-05 | 0.00405954 | intron-variant | SAE1 | GRCh38.p7 | 19:47203634 | GGTCACAGTTCTGTT[A/C]CCAGTGCTCCATTTT | 10055 |
| rs376061149 | in-del | -/AGACG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47169434 | ATATTTGTAGAGACG[-/AGACG]GGGGTTTCACCATGT | 10055 |
| rs376081696 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47178295 | ATCACTGAGGAAACC[A/G]TTGAAAAATGCGGAG | 10055 |
| rs376086221 | snp | C/T | 0.000217976 | 0.0104375 | utr-variant-5-prime, nc-transcript-variant, missense, intron-variant | SAE1 | GRCh38.p7 | 19:47130902 | TTGGCTTGAGCGGGA[C/T]CGGAGCTGAGGCAGG | 10055 |
| rs376143365 | snp | A/G | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47155204 | TTCTGAGACAACGAT[A/G]GTCAAAAAGGTATGT | 10055 |
| rs376184177 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47209041 | TGCCAAATAGCCCTT[C/T]GGGAGCAAAATCGAC | 10055 |
| rs376226945 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47186437 | AGGTAATTCATTCAG[C/T]GGGTAAGGGTCAGGA | 10055 |
| rs376236726 | snp | C/T | 6.58913e-05 | 0.00573945 | stop-gained, utr-variant-3-prime, synonymous-codon, nc-transcript-variant, missense | SAE1 | GRCh38.p7 | 19:47209203 | CAACTTCTTCTTCTT[C/T]GATGGCATGAAGGGG | 10055 |
| rs376242752 | snp | C/T | 1.64751e-05 | 0.00287007 | synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47143591 | AAAGGACTGACCATG[C/T]TGGATCACGAACAGG | 10055 |
| rs376267776 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47161005 | TATATTTAATTTTAT[A/G]TGTTATTTATTTTTG | 10055 |
| rs376278271 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47191947 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 10055 |
| rs376284799 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47183111 | AGTGGAGATGGGCTT[C/T]CACCATGTTGGCCAG | 10055 |
| rs376336281 | snp | A/G | | | intron-variant, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197241 | TTCCCAGTGCTCTTA[A/G]AGTTCCGTACAGATA | 10055 |
| rs376417031 | in-del | -/T | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176944 | ACTGTGAGTTTATCA[-/T]TAACAGGAGTGCTAA | 10055 |
| rs376432419 | snp | A/G | 1.66477e-05 | 0.00288506 | intron-variant | SAE1 | GRCh38.p7 | 19:47150378 | TCAATTCGATGCTGT[A/G]AGTTTCTTATTATAA | 10055 |
| rs376443579 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47198573 | TGTACTAGGCATCAG[A/G/T]TAGTAAGTAGCCAAC | 10055 |
| rs376495876 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47207140 | TCCCAGCTACTCAAG[A/T]GGGTATGGGAGGATA | 10055 |
| rs376550404 | in-del | -/TAC | | | intron-variant | SAE1 | GRCh38.p7 | 19:47196373 | TTTTTTTTTTAATTT[-/TAC]TTTTTTGAGACGGAG | 10055 |
| rs376581089 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47206204 | CAGATAGCCAGAGTA[C/T]TCTGCATTCTTCGTT | 10055 |
| rs376626611 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47149053 | AGGGCCTCTCTGTGT[G/T]GTCCAGGCTAGTCTT | 10055 |
| rs376664496 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47181966 | CTAAATTTTTAATTT[A/T]ATTGTAGAGAGGCCT | 10055 |
| rs376667788 | in-del | -/CCT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47183025 | GGTTCAAGCAATTCT[-/CCT]GCCTCTGCCTCCCGA | 10055 |
| rs376690748 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184865 | GTCTCACTCTGTCCC[C/T]CAGGCTGGAGTGCAG | 10055 |
| rs376699582 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47139586 | GCTGTGAATGTGTAT[C/T]TTTTTTTTTTTTTTT | 10055 |
| rs376720327 | snp | A/G | 6.59631e-05 | 0.00574258 | intron-variant | SAE1 | GRCh38.p7 | 19:47143610 | ATCACGAACAGGTGC[A/G]CTGTTGTGAGCTCAT | 10055 |
| rs376744881 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47143739 | ATAAACCATTGCCTC[G/T]GGAGACTGAAGGTGC | 10055 |
| rs376753684 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47181757 | GTGCTGGGATTATAA[A/G]TGTGAGCCAGTGCAC | 10055 |
| rs376765172 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47173218 | TGGCCAGGCTGGTCT[C/T]GAACTCTTGACCTCG | 10055 |
| rs376832785 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47144636 | CCTGGGAGGCGGAGC[C/T]TGCAACGAGCCGAGA | 10055 |
| rs376843575 | snp | A/G | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190328 | AGGTGCTCTTCAGAA[A/G]TGCAGTCAACAGTGG | 10055 |
| rs376849069 | in-del | -/CT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47162939 | GTAGGCAGCAGTGAG[-/CT]GAGATTGTGCCACTG | 10055 |
| rs376857109 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47193994 | GAAGCAGGGTGTGTC[-/T]TTTTTTTTTACCTGG | 10055 |
| rs376915464 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47142840 | TCTGTCTCAAATAGC[A/G]TTCTCCATCATTCTT | 10055 |
| rs376951250 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47202416 | CCTCAACCTCCTGAG[C/T]AGCTGGGACTACAGG | 10055 |
| rs377026323 | in-del | -/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47194635 | CTCGAGACTGGCTGT[-/G]GCCCTTTCCTTGGGC | 10055 |
| rs377070055 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47207226 | GTAGCAGAACAAGAT[C/T]CTATCTCAAAAAATT | 10055 |
| rs377089416 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167575 | GTCAAATCTATATGC[A/G]TCCTTAGCAAGCTTT | 10055 |
| rs377168727 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47179241 | CCGGTCGCGATGGCT[C/G]ACGCCTGTAATCCTA | 10055 |
| rs377249289 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47197556 | TAAAAAATAAAGAGG[A/G]GACAGATTCTGATTT | 10055 |
| rs377351793 | snp | A/T | 0.000574382 | 0.016937 | intron-variant | SAE1 | GRCh38.p7 | 19:47197195 | CCAAAAAAAAAAAAA[A/T]GTGGCTTTATAACCT | 10055 |
| rs377363244 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47191970 | GAGGCAGGAGAATGG[C/T]GTGAACCCGGGAGGC | 10055 |
| rs377401612 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47132889 | GTGAGGCCCCGTCTC[-/A]AAAAAAAAAAAAAAA | 10055 |
| rs377423093 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant, synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197355 | GGTATTAGTCCTGAC[C/T]TGCTTCCTGAGGACT | 10055 |
| rs377463153 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47161963 | CCATTTTGGTAGCCA[C/G]TAGCCACAGCTGGCT | 10055 |
| rs377482319 | in-del | -/GA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47175106 | TTTAAAAGTGGCCTT[-/GA]TTTTTTTTTTTTTTT | 10055 |
| rs377558723 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47132260 | GAGCCACTGTGCCCA[C/G]CTTGTTTTTTTTTTT | 10055 |
| rs377563068 | in-del | -/AATTTTACAGAA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47181802 | TTTTTTTTTTTTTTT[-/AATTTTACAGAA]TTTTTTTTTTTTTTA | 10055 |
| rs377618600 | snp | C/T | 9.90917e-05 | 0.00703818 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209271 | AAGATTTGGCAGCCC[C/T]AGAGATGCCAACTGC | 10055 |
| rs377634387 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SAE1 | GRCh38.p7 | 19:47194994 | GTGATCTGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 10055 |
| rs377639806 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47152586 | CTAAGTTATTTTTTT[-/T]ATGAGAACTATGAAA | 10055 |
| rs377640369 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47136572 | GTGATCTCAGCTCAC[C/T]GCAACCCTTGCCTCC | 10055 |
| rs377649958 | snp | C/T | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130770 | TCTCGTGAGGTACTT[C/T]TGGTCCCAGGCTCCG | 10055 |
| rs377698907 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167207 | GATCCACCCGCCTTG[A/G]CCTCCCAAAATGCTA | 10055 |
| rs377707107 | snp | C/T | 0.000121459 | 0.00779197 | intron-variant | SAE1 | GRCh38.p7 | 19:47150193 | AAAAAATATGTGTAT[C/T]ATTCCTAGGTAACTC | 10055 |
| rs377757100 | snp | C/T | 0.000303378 | 0.0123125 | intron-variant | SAE1 | GRCh38.p7 | 19:47153084 | TAACATTTTCTCCTT[C/T]TTATACTTTTTTTTT | 10055 |
| rs386809909 | multinucleotide-polymorphism | CT/TG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47149949 | TTGTGGTGGTGCGTG[CT/TG]TGTAGTCCCAGCTAC | 10055 |
| rs386809910 | in-del | AGA/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47193849 | AAAAAAAGAAAGAAA[AGA/G]AAAAGAAAAAGAAAT | 10055 |
| rs386809911 | multinucleotide-polymorphism | CA/TG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47201464 | GCAACCTCTGCCTCC[CA/TG]GCTTTAAGTGATTCT | 10055 |
| rs397733710 | in-del | -/T | 0.375 | 0.216506 | intron-variant | SAE1 | GRCh38.p7 | 19:47205337 | TTTTTTTTTTTTTTT[-/T]GTCTATTTTTTCTGA | 10055 |
| rs397756488 | in-del | -/CTTG/CTTT/CTTTC | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129824 | TTTCTTTCTTTCTTT[-/CTTG/CTTT/CTTTC]TTTTTTTTTTTTTAC | 10055 |
| rs397798378 | in-del | -/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47146051 | AGAACAAGGAGGGTT[-/T]GTCAAGATAAGAGCC | 10055 |
| rs397859510 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47160389 | ACCACGCCCAGCTAA[-/T]TTTTTTTTTTTTTTT | 10055 |
| rs398034851 | in-del | -/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47147227 | TTTTTTTTTTTTTTT[-/T]GAGGCAGTCTCACTG | 10055 |
| rs398034852 | in-del | -/A | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47150095 | AAAAAAAAAAAAAAA[-/A]TTTAGGTGGTAGGTA | 10055 |
| rs398034853 | in-del | -/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47161197 | TTTTTTTTTTTTTTT[-/T]GAGATCTCTTGCTGT | 10055 |
| rs398034854 | in-del | -/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47181801 | TTTTTTTTTTTTTTT[-/T]AATTTTACAGAATTT | 10055 |
| rs398034855 | in-del | -/A | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47188361 | TCTCAAAAAAAAAAA[-/A]GAAAAAAATAATCAC | 10055 |
| rs398034856 | in-del | -/C/CCCT/CCTTT/CT | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47204509 | GCCGCACCCCCCCCC[-/C/CCCT/CCTTT/CT]TTTTTTTTTTTTTTT | 10055 |
| rs527269373 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47168082 | TCTGTAATCCCAGCT[A/C]CTGGGGGCGCTGAGG | 10055 |
| rs527302486 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SAE1 | GRCh38.p7 | 19:47167519 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGCC | 10055 |
| rs527341318 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47173310 | CCCAAAGTCTTGTTC[A/G]GAACAACCATGCACC | 10055 |
| rs527373884 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47171150 | CAGCTAATTTTTATA[G/T]TTTTAGTAGAGACAG | 10055 |
| rs527394464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47133460 | TCGATCTCCTGACCT[C/T]GTGATCCGCCTGCCT | 10055 |
| rs527457334 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47155048 | GTGACCTGGAGAGGC[A/T]TTTTTTGATTCCAAT | 10055 |
| rs527508932 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167899 | AGCTAGTTCTAAGAA[C/T]TGCTTTTTTCTGGCT | 10055 |
| rs527521322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47195401 | TTGGGATAAAAGTTA[C/T]AGCCTTGTTGGGGTC | 10055 |
| rs527570079 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210352 | AAGAGTTAAATTGTT[C/T]ACATTCTAGAATGTG | 10055 |
| rs527604236 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47199623 | CACTTTGAATGCCCA[A/G]GTAGTCACTTGGCTG | 10055 |
| rs527604810 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47164458 | AGGCATGAGCCACCA[C/T]GTCTGGCCTGGAGCG | 10055 |
| rs527675402 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47182566 | GACCACAGTCATTCA[C/G]AAAGGAAGAAGGCAC | 10055 |
| rs527723277 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47177908 | CCTCGGAGGGGACTG[C/G]AGCTTGGAGAGAGCA | 10055 |
| rs527781388 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47196256 | TGGTCAGGCTGGTCT[C/G]AAACTCCTGACCTCG | 10055 |
| rs527784690 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47188814 | CCAGGCCAGGGACAG[C/G]CTTTGCAGAGAGAAG | 10055 |
| rs527795772 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SAE1 | GRCh38.p7 | 19:47154410 | ATTATAAAGAAGTTA[C/T]AGTAGTGGGAAGCAA | 10055 |
| rs527813310 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SAE1 | GRCh38.p7 | 19:47148658 | CTCACTCTGTTGCCC[A/T]GGCTGGAGTGCAGTG | 10055 |
| rs527860252 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47180626 | CAGGAGTTTTGAGAC[C/T]AGCCTGGGCAACAAA | 10055 |
| rs527866648 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47162725 | GCTGGGTGCAGTGGC[A/T]CATGCCTGTAATCCC | 10055 |
| rs527900416 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SAE1 | GRCh38.p7 | 19:47169518 | CCAAAGTGTTGGGAT[C/T]ACAGGTGTGACCCAC | 10055 |
| rs527964153 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129197 | GCACTTTGGGAGGCC[A/G]AGGCGGGTGGATCAC | 10055 |
| rs528054844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47197688 | CTCTTGGGGACATCT[C/G]CAGATCAGTACATAG | 10055 |
| rs528079606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47149478 | GCCCTGCCCACACTG[A/G]TCTAGTTTTAAACCA | 10055 |
| rs528121790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47155499 | GGAATTTTTTCTTGT[C/T]GCTCAGGCTGGAGTG | 10055 |
| rs528177905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47204476 | GTGCTGGGATTACAG[C/G]CATGAGCCACTGTAC | 10055 |
| rs528198144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47205438 | ATATTTGGAGGGGGA[A/G]GAAAAGTGTGCAATG | 10055 |
| rs528207973 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47187380 | GTATCTGCTGCTGCT[G/T]TTTTCTTTTTTTCTT | 10055 |
| rs528221528 | in-del | -/T | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176836 | GCAAAAGGTCTCTTC[-/T]TTTTATTATTCTCCC | 10055 |
| rs528231624 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SAE1 | GRCh38.p7 | 19:47137353 | AGGTCACACTATCGC[A/G]CTCCAGCCTGGGTGA | 10055 |
| rs528232338 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SAE1 | GRCh38.p7 | 19:47155773 | TTTTTTTTTGAGATG[A/G]AGTCTTGCTGTGTCC | 10055 |
| rs528250611 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130149 | CGCTCCTCTCTCCCA[C/G]TGGGCCGTGACTGCC | 10055 |
| rs528264403 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47177101 | CAATCTTAACTTGCT[C/G]AGTCTCTGTTCTGAT | 10055 |
| rs528359226 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47143780 | TTTGAATTCTAGCTC[C/T]ACCACATCTAGCTGG | 10055 |
| rs528359909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191784 | GAATAGGCCGGGCGC[A/G]GTGGCTCACACCTGT | 10055 |
| rs528384168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47136465 | ATTTGGGTATATACC[C/T]AGCAGTGGGATTGCA | 10055 |
| rs528397860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47143417 | GCAAACCAAAATGAT[C/T]TGTGTATTTTTTGTT | 10055 |
| rs528448206 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47165035 | TGTGATCCACTCACC[C/T]TGGCCTCCCAAAGTG | 10055 |
| rs528462255 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47141909 | TACATGATGTAAAGT[C/T]TGTATTTCCTTTTTG | 10055 |
| rs528464610 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47157383 | GGAGTACAAAAGCTG[C/T]TTTGTGGGTGCTGTC | 10055 |
| rs528486068 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47149014 | TTTTCTCATGAGGTT[A/G]CAATTTTTGTTGTTT | 10055 |
| rs528517917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47171121 | CTGGGACTGCAGGCG[C/T]GTGCCACCACACCCA | 10055 |
| rs528599475 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47130851 | CTCCGGGCGTGCTGC[A/C]GGCGGCGGTAGGTGG | 10055 |
| rs528647954 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47200016 | GCTCACTGCAAGTTC[C/T]GCCTCCCGGGTTCAC | 10055 |
| rs528681947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47151759 | TCTTCATTTTCTTAT[C/T]TGTAGTAACCACATT | 10055 |
| rs528696923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47192373 | CCTGCCTCAGGCTCC[C/T]GAGTAGCTGGGATTA | 10055 |
| rs528768054 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47207143 | CAGCTACTCAAGAGG[A/G]TATGGGAGGATATCT | 10055 |
| rs528904917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47178640 | ACCATGCCTGGCTAA[C/T]TTTTGTATTTTTAGT | 10055 |
| rs528993927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47138797 | GACTAGCTTGGGCAA[C/T]TTAGTGAGGCCCCAT | 10055 |
| rs529026465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47145224 | TCAAGCTGGTCTTGA[A/G]CTCCGACCTCAGGTG | 10055 |
| rs529031678 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47208705 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCC | 10055 |
| rs529179958 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47132427 | CGACTAATTTTTGTT[G/T]TTTTTTTTTTTTGTA | 10055 |
| rs529250022 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47166175 | ATGCTTAGGCCAGAG[A/T]CGTGGGGGTTTGGTG | 10055 |
| rs529255387 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47146854 | GTGGACTCCGGAGAC[A/C]GCACACAGAAGCAGG | 10055 |
| rs529293972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47153644 | TCTCTTGTTCAGCCT[C/T]TCAGGCAAGTCACTG | 10055 |
| rs529302556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47187958 | GCCAGGTGTTCAGTA[C/T]AGAGTAGTGACATCG | 10055 |
| rs529359214 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47201247 | AGAGATGGGGTTTCA[C/T]CATATTGGCCAGACT | 10055 |
| rs529378660 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209537 | CTTCCAAGCACCCCT[A/C]TGCCCTTTCTCTGTC | 10055 |
| rs529475296 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47174025 | TCCTGACCTCGTGAT[C/G]CACCCGCCTCGGCCT | 10055 |
| rs529488255 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47173393 | CACCCCTCCAACCCC[A/G]TAACTTCTGATGCTG | 10055 |
| rs529513000 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47181062 | TGGCTCACGCCTATA[A/C]TCCCAGCACTTTGGG | 10055 |
| rs529524104 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47180540 | GTTTCCTTATCAGAT[C/G]CTTTTATGCTATGCC | 10055 |
| rs529537222 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47133567 | CAGAATAGGTTAAAG[G/T]GGTCAGAAATGGAAG | 10055 |
| rs529539195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47141281 | TGCTGGGATTACAGG[C/T]GTGAGCCCCCACGCC | 10055 |
| rs529557164 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47178503 | TTTTTGAGACAGAGT[C/G]TAGCTTTGTTGCCCA | 10055 |
| rs529574711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47188546 | GTGTATCGGCTTTTC[C/T]AGGGCGAGTGTGAGC | 10055 |
| rs529575414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47140738 | AGGTTGAGGCTGCAG[C/T]GAGCCCTGATCTTGC | 10055 |
| rs529613148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47161652 | TTAAGAATGATTTCG[C/T]TCACCATCATAGACC | 10055 |
| rs529613965 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47203097 | GATTTGCTTACTAGG[A/T]TGGGTAACTTGGAGG | 10055 |
| rs529627806 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47154751 | CACGCCCGCCTTGGC[C/G]TCCCACAGTGCTGGG | 10055 |
| rs529650744 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47168520 | GCTGTTATTTGACTC[A/C]TGGACTCAGGTGATC | 10055 |
| rs529650797 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47160808 | TGCTGGGATTACAGG[A/C]GTGAGCCACCACTCC | 10055 |
| rs529756936 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SAE1 | GRCh38.p7 | 19:47167529 | ACAGGTGTGAGCCAC[C/T]GCGCCCAGCCAACAA | 10055 |
| rs529831612 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210550 | GATGCAGCCAAAGTG[C/T]GTTCCAGTTCACCCC | 10055 |
| rs529836830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190630 | GCGAGGTATGTGGAT[A/G]GTGCCAGCCTGCCGG | 10055 |
| rs529837174 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47182265 | CCTTTGCAAAGCAGG[C/G]CATAGGCAGCCATCG | 10055 |
| rs529919583 | in-del | -/TCTA | 0.00557542 | 0.0525036 | intron-variant | SAE1 | GRCh38.p7 | 19:47148918 | CGCACCTGGCCATAG[-/TCTA]TCTATGTTTTTTAAA | 10055 |
| rs529992907 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, missense, synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47203704 | GGCCCCAGTGTGTGC[A/G]GTGGTTGGAGGGATT | 10055 |
| rs529996722 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47148702 | TCAATGCAGCGTCTG[C/G]CTCCCAGGTTCAAGC | 10055 |
| rs529998576 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47205439 | TATTTGGAGGGGGAA[A/G]AAAAGTGTGCAATGG | 10055 |
| rs530030358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47196469 | GCTGGATTCAAGTGA[C/T]TCTCCTGCTTCAGTC | 10055 |
| rs530092469 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47169551 | CGCCTGGCCCAGTGA[C/G]AGTTAAAGGGCCAGA | 10055 |
| rs530093438 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | SAE1 | GRCh38.p7 | 19:47162578 | AGCTTTTTAAAGATT[C/G]TTGGTCCCTCTACCC | 10055 |
| rs530094628 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47182767 | ATTAGATGAAGGCCT[C/G]GCACACATTGTGAAT | 10055 |
| rs530130437 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47175647 | GGAGGCTGAGGTGAG[A/G]GAATCTCTTGAACCT | 10055 |
| rs530147017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47172013 | CAACCTCCACCTCCC[A/G]GTTCAAACAGTTTCC | 10055 |
| rs530155398 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47188010 | AAATCTAATGGAGGA[C/G]ACAAGCCAGTCCTTG | 10055 |
| rs530234773 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47203518 | CAGATTTCATTTTCA[C/T]GCCTAGATGCCAGCA | 10055 |
| rs530239368 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47139470 | GGATTACAGGTGTGA[C/G]CCACTGCGTCCAGCC | 10055 |
| rs530249778 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47142932 | GTCTCCTACTTTTTC[A/G]TGAGGGCAGGGACTA | 10055 |
| rs530325008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47163815 | TTTAGAGACAGAGTC[C/T]TGCTTTATTGCCCAG | 10055 |
| rs530383247 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47143834 | CCTCATTGAGCTTGC[C/G]TGCCTGTAAAATGGG | 10055 |
| rs530426431 | in-del | -/TGT | 0.0166325 | 0.0896639 | intron-variant | SAE1 | GRCh38.p7 | 19:47168601 | ACTCAGCCATAAATG[-/TGT]TGTTGTTGTTGTTTT | 10055 |
| rs530439267 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129902 | GCTTACTACAACCTC[C/T]GCCTCCCGGATTCAA | 10055 |
| rs530456759 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47191826 | TTTGGGAGGCCAAGG[A/C]GGGCCGATCACAAGG | 10055 |
| rs530512808 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47206314 | CTGCTCTCATCCCCA[G/T]TACTCCTTCATACTT | 10055 |
| rs530515581 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47184971 | ATTACAGGTGCCCAC[C/G]ACCATGCCCAGCTAA | 10055 |
| rs530593004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191504 | CTGCCTGAGCAGATG[A/G]AGGCAAAGCTGTGCA | 10055 |
| rs530625684 | snp | A/G | 1.64866e-05 | 0.00287106 | intron-variant | SAE1 | GRCh38.p7 | 19:47143478 | TATCATCAGGTTAAC[A/G]ATGTTTGTCTTACAG | 10055 |
| rs530660533 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47131366 | ATAAGAGGGGCTGGG[C/G]ATACGTGGAAAGGGT | 10055 |
| rs530661925 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150310 | CTCAACCCCATGGTG[A/G]ATGTGAAGGTGGACA | 10055 |
| rs530695903 | snp | A/C/G | 0.0023933 | 0.0345097 | utr-variant-5-prime, nc-transcript-variant, missense, intron-variant | SAE1 | GRCh38.p7 | 19:47130866 | CGGCGGCGGTAGGTG[A/C/G]CGCGCGGGTCCGGCG | 10055 |
| rs530696026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47138115 | ATGGCGTGATCTAGA[C/T]TCACTGCAACCTCTG | 10055 |
| rs530752664 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47171231 | GCCCACCTCAGCCCC[C/G]CAAAGTGCTGTGATT | 10055 |
| rs530783037 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47158650 | AGAGTTGCTGTGGCT[A/G]CCCTCACTGCCGCAG | 10055 |
| rs530783712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47177280 | CCAATGTGAAAGACA[A/G]ACAAATAATTCTACT | 10055 |
| rs530783786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47185634 | TGAGACAGAGTCTCA[C/T]TGTGTCTCCCAGGCT | 10055 |
| rs530784847 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47151859 | TTGATTGTGTAATGC[C/G]TGTGCATGGGGCCAT | 10055 |
| rs530853595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47144470 | TTTGGGAGGCTGAGG[C/T]GGGCAGATCATGAGG | 10055 |
| rs530882024 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47208091 | ATAGCCCCCGCTTCT[A/G]CATCAGTGTGTTCCT | 10055 |
| rs530941193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47165769 | TATGAGTTAGTTTGA[A/G]CCAAAAGGATTGTTA | 10055 |
| rs530952742 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47165147 | GGAGTACAGTGGTTT[C/G]ATTGTGATCTCGGCT | 10055 |
| rs530963000 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47139106 | ACAGGCACGTGCCAC[C/T]ACGCCTGGCTAATTT | 10055 |
| rs531004345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47186840 | GTAGTCTTCATGGGC[A/G]GCCACTCCAGAGGTG | 10055 |
| rs531041366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47186584 | CTGGTCTTTAATTTG[A/G]TAAGCAAAAAATGGC | 10055 |
| rs531081703 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47193056 | TCTAGATGGTCACAG[A/C]CTTTTTTTTTTTTTT | 10055 |
| rs531092748 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47145818 | GCCACTGCACCCATC[G/T]TAGAGCGTATTATGT | 10055 |
| rs531102386 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47151934 | TATAGTTACTTTAGA[C/T]TCTGCAGGGTTCCAT | 10055 |
| rs531104420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47200131 | GTAGAGATGTGGTTT[C/T]GCTGTGTTAGCCAGG | 10055 |
| rs531106521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47145304 | CCGCACCCGGCCATG[C/T]CTGGCTAAGTTTTGT | 10055 |
| rs531142121 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47152206 | AAGATGGTATTTTGT[G/T]CAGTAGAACTTAGCC | 10055 |
| rs531166284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47193785 | TTGAGCCGAGATCAC[A/G]CCATTGCACTCCAGC | 10055 |
| rs531194613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47166967 | TTGAACTTTTTTTTT[C/T]TTGAGACGGCGTCTC | 10055 |
| rs531228250 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47172921 | ACCAGCTACAGAGGG[G/T]AATCTGAGGCTCAGG | 10055 |
| rs531266648 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47201003 | GCTGGGATTACGGGC[A/G]TACGCCACCATGCCC | 10055 |
| rs531319273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47173249 | TGAACCGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 10055 |
| rs531362143 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47210162 | TTGGTTCTTTTTAAA[A/G]GAATGATAATAAAGT | 10055 |
| rs531453065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47139811 | TTTTACCATGTTAGC[C/T]AGGATGATCTCAATC | 10055 |
| rs531464456 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47203253 | CCCTTGCTTCCTACA[C/T]GTTAACACAGGCCTG | 10055 |
| rs531508755 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47160674 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGTGCC | 10055 |
| rs531521649 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209700 | AAAGTGTGAATTCAG[A/G]TGGAGAGTAGGCCCA | 10055 |
| rs531528586 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47171262 | ACAGGTGTGAGCCAC[C/T]GCGCCTGGCAAACCT | 10055 |
| rs531592964 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47168883 | TGCTAGGATCACAGG[C/T]GTGAGCCACTGTGCC | 10055 |
| rs531648209 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47195013 | CTCCCAAAGTGCTGG[G/T]ATTACAGACGTTACA | 10055 |
| rs531681085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47167487 | CCTTGTGATCTGCCC[A/G]CCTTGGCCTCCCAAA | 10055 |
| rs531685230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47141362 | GGACAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 10055 |
| rs531686843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47202884 | CACTGCACTCCAGCC[C/T]GGGTGACAGAGCGAG | 10055 |
| rs531734293 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47139455 | CCTCCTAAAGTGCTG[A/G]GATTACAGGTGTGAC | 10055 |
| rs531765106 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47142977 | CCTTATTTCCACACC[A/G]TAGAAGGATGCCTGG | 10055 |
| rs531800589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47195095 | AGTCTCACTCTGTTG[C/T]CCAGGCTGGAGTTCA | 10055 |
| rs531827481 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47144851 | TTTGTGTGTTTTTGC[G/T]AGACGAGTCTTGCTG | 10055 |
| rs531852729 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47180571 | TGGTGGCTCACCCCT[A/G]TAAATCCCAAGAGGC | 10055 |
| rs531878262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47154534 | GACTTTCACTCAGTT[A/G]CCCAGGCTGGAGTAC | 10055 |
| rs531918829 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47168619 | TGTTGTTGTTGTTTT[G/T]GAGACAGAGTTTCGC | 10055 |
| rs531928089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47141937 | TTGAAATCTGAAAAA[A/G]TTGTGACTCTGAAAT | 10055 |
| rs531953111 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47155727 | GATTACAGGCGTGAG[C/T]CACCATGCCCGGCCC | 10055 |
| rs532002373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47174304 | TTTTCTTTTTCTTTT[C/T]TTTTTTTTTTGGTGT | 10055 |
| rs532021811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47162672 | TGCAGAATTATATTA[C/T]TTGTTACTGTTAGGC | 10055 |
| rs532035939 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47179884 | TTTCACAGTGATAGG[A/G]GTTAGCAATTCTGAA | 10055 |
| rs532101703 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47204426 | GATGGTCTGGATCTC[C/G]TGACATCGTGATCTG | 10055 |
| rs532153762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47169433 | GTATATTTGTAGAGA[C/T]GGGGGTTTCACCATG | 10055 |
| rs532168173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47143348 | GACCTCAAGTGATCC[A/G]CCTATCTCAGCCTCC | 10055 |
| rs532194916 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47145228 | CTGGTCTTGAACTCC[-/T]GACCTCAGGTGATCC | 10055 |
| rs532205676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47182950 | TGAAACAGTCTCGTT[C/T]TGTCAGCCAGGCTGG | 10055 |
| rs532238442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191400 | GTTAGTATAGCCAAA[A/G]CAGAGGATATTGCAT | 10055 |
| rs532254011 | snp | A/C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47159992 | AGCCACAGCTTCCAG[A/C/T]CTGATTGTTTCCATT | 10055 |
| rs532266701 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47203859 | CCATTCATCTTTGTT[G/T]CATGCCCTCCCCATT | 10055 |
| rs532287099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47135904 | CGCCTCCCAGGTTCA[C/T]GCCATTCTCCTGCCT | 10055 |
| rs532307751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47149401 | GTCTCAAACTCCTGA[C/T]CTCAGGTGATCCTCC | 10055 |
| rs532515249 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47163847 | CTGGAGCGCAGTGGC[A/G]TGATCTCCGTCTCCC | 10055 |
| rs532527540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47198438 | TTCCAAGCAGCTCTG[A/G]GATCATGTACACACC | 10055 |
| rs532555382 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47170105 | GGTCTACCATTGAGC[G/T]CTGGGTTCTAATGAC | 10055 |
| rs532584204 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47200023 | GCAAGTTCCGCCTCC[C/T]GGGTTCACGCCATTC | 10055 |
| rs532590556 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | SAE1 | GRCh38.p7 | 19:47130820 | GCGTGGGAGGGTCTG[C/T]GCATGCGCAGAAGCA | 10055 |
| rs532607268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47157243 | ACAGAACCATAATTA[C/T]CCAGAGTGAACCTTG | 10055 |
| rs532687658 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47206401 | GACTCACCTTTCTCT[C/T]CTGAGGCACTGTCTG | 10055 |
| rs532859134 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47199412 | AAAAAAAAAAAAAAA[A/T]AGGCAGCAATAGAGT | 10055 |
| rs532935931 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47186330 | TCTATTGGTAAGTAC[A/C]ATGCAAATATTTCAA | 10055 |
| rs532951804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47177930 | GAGAGAGCAGGCTAG[C/T]GGTTTCCCTATTGAT | 10055 |
| rs533050954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47191876 | CTGGCTAACACGGTG[A/G]AACCCCGTCTATACT | 10055 |
| rs533086208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47143967 | GTGGCCTGGAGGCTT[C/T]GTGGTGCCCTAGCTT | 10055 |
| rs533098002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47151596 | CTGCCTCAGCCTCCC[A/G]TTTTTACACTTTTCT | 10055 |
| rs533216573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47178559 | GCTCATTGCAACCTC[C/T]GCCTTTTGGATTCGT | 10055 |
| rs533233499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47132209 | CTCAAGTGATCTGCC[C/T]GCCACAGCCTCCCAA | 10055 |
| rs533252538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47208231 | AACACAGTGTTAGTC[A/G]TTGTTTTAGTTTTAA | 10055 |
| rs533271500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47138739 | TGTGATCCCAGCTAC[C/T]GGGGAGGCTGAGGTT | 10055 |
| rs533324199 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47201095 | CACCCAAGCTAGAGT[A/G]CAATGGCCCGATCTT | 10055 |
| rs533364301 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47159469 | AGTGTGTAGCACAGT[A/C]ATATCCACGGAATAT | 10055 |
| rs533445157 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47146782 | TGGACCACTCTCATG[G/T]AAATAGCAAGGATAT | 10055 |
| rs533457090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47140057 | ATTCTCCTGCCTCAG[C/T]TTCCCGAGTAGCTGA | 10055 |
| rs533490507 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47208654 | GGTCTCCAACTCCCA[A/G]CCTCAGGTGATCCGC | 10055 |
| rs533519529 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47140674 | AGTGGTGTGCACCTA[C/T]AGTCCCAGGACTCAA | 10055 |
| rs533598577 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47167053 | ACCTCCTGGGTCCAA[G/T]TGATTCTGCTCCCTC | 10055 |
| rs533603507 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47187817 | GTGAGCCACTGCACC[C/T]GGCCTCTGGATTGCC | 10055 |
| rs533607182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47159039 | TCTGTGTTAGGTGCT[A/G]CCAGAGATGATGAGA | 10055 |
| rs533627650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47208496 | CCCAGGCTGGAGTGC[A/G]GTGGCGCAATCTCAG | 10055 |
| rs533670292 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47194049 | GGAACACTTTATAAC[C/T]CATTTCTGAACGTCT | 10055 |
| rs533673332 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47173875 | CTGCAAGCTCAGCCT[C/T]CTGGGTTCACGCCAT | 10055 |
| rs533757015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47140327 | TAGCCAGGATGGTCT[C/T]GGTCTTCTGACCTCG | 10055 |
| rs533795123 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47188509 | TAAATGAGCTACTGT[A/G]TGACACAGGTTACCA | 10055 |
| rs533812860 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47194783 | GAGATGGAGTTACGC[C/T]CTATCGCACAGGCAA | 10055 |
| rs533822069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47187309 | GCCCTCAGATGCAAC[A/G]GTGAAAGTGGGACTC | 10055 |
| rs533846938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47194407 | TTATGTAGGAACCCT[C/T]GTCCTGGTAGAGAGT | 10055 |
| rs533901033 | snp | C/T | 4.96537e-05 | 0.00498241 | intron-variant | SAE1 | GRCh38.p7 | 19:47209144 | GCTAAACCCTCTTTT[C/T]ATTTTTCTCCCCAGG | 10055 |
| rs533946987 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47140907 | GGGATGGAGTGCAGC[A/G]GCACAGTCTTGGCTC | 10055 |
| rs533974063 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SAE1 | GRCh38.p7 | 19:47202177 | TTATTTCGACGCCTG[C/T]GTCTTTGTCAAGATG | 10055 |
| rs534001846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47181248 | TTGAACCCAGGAGGC[A/G]GAGGTTGTGGTGAGC | 10055 |
| rs534033095 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47188177 | AACATGGTGAGACCT[C/T]GTCTCTACAAAAAAT | 10055 |
| rs534082549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47203979 | CATAGTGCCTCGAAG[G/T]TGTGATCTGCTCTCC | 10055 |
| rs534110086 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47155383 | GCTGTTGCTGTGAGG[G/T]AATGTGGGCCCAGTG | 10055 |
| rs534117490 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47200949 | TGCAACCTCCACCTC[A/C]CGGGTTCAAGTGAAT | 10055 |
| rs534176423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47168247 | TGTGTGTTTATATGC[A/G]AACCATTTGTGAAAG | 10055 |
| rs534211713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47174427 | CTGAGATGGAGTTTC[A/G]CTCTTGTTGACCAGG | 10055 |
| rs534247591 | snp | C/G | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129355 | GCTGGAGTGCAGTGG[C/G]AGGATCTTGGCTCAC | 10055 |
| rs534249657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47173558 | TCCTCACTTCAGCAC[A/G]CTACTGACATTCTGT | 10055 |
| rs534302227 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47180813 | GGGAGCAAGACTTTG[A/T]CTCCCCCGAAAAAGA | 10055 |
| rs534321651 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47183112 | GTGGAGATGGGCTTT[C/T]ACCATGTTGGCCAGG | 10055 |
| rs534325314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47142340 | AGTGAGCTGAGATCA[C/T]GCCACTGCACTCCAG | 10055 |
| rs534338236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47134011 | GGGATTACAGGCGCC[C/T]GCCACCATGCCCAGC | 10055 |
| rs534441708 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47170039 | TGGCATTCTTCATTG[G/T]CTAGTTCTCAGTGAT | 10055 |
| rs534443468 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47195959 | GGATTATCTCAAACT[C/G]CTGGGCTCAAGCGAT | 10055 |
| rs534452368 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47203869 | TTGTTTCATGCCCTC[A/C]CCATTTCCACCTCAT | 10055 |
| rs534484950 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210763 | AAAGGATCCGTGTCT[C/T]GCCACCTTTAGTGCA | 10055 |
| rs534500525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47163391 | TAACAACTGTTTACA[C/T]AGCAATTCCATTAGG | 10055 |
| rs534573979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47175771 | ATCTCTAAACTAATA[C/T]ATCTCATTAAATTTC | 10055 |
| rs534607822 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129456 | TGTGCCACCACGCCC[A/G]GCTAATTTTTTAGTA | 10055 |
| rs534608344 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47175237 | GGCACTACTCTTGTT[A/T]CCATGTTCCTGGCAC | 10055 |
| rs534644558 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47135952 | GGGACTACAGGTGCC[C/T]GCCACCACGCCCGGC | 10055 |
| rs534649755 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SAE1 | GRCh38.p7 | 19:47182492 | GTGTGTGTGTGTGTG[C/T]GTGTGCGCGCACGCA | 10055 |
| rs534652914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47198030 | ATGCTTTCACCTTAC[A/G]TGACTACCTTTTTGC | 10055 |
| rs534657215 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47145506 | CCAATGTAGCTTTCT[C/T]TGACCAGGCTCATCT | 10055 |
| rs534681433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47190034 | ACGTGAAACCGTGCT[C/T]GGTTTCTCTTTTCCA | 10055 |
| rs534685644 | snp | A/C | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190279 | ACAGTGTTTGATCTT[A/C]ACGGAACAGTTTTAT | 10055 |
| rs534690939 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47150537 | GTTTAGGCTTAGTAT[A/G]TTGTGTGAATGTGTT | 10055 |
| rs534722967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47152524 | GTTTTGCTTGTCCCT[A/G]TAGCTTATTTGGATT | 10055 |
| rs534724321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47156719 | AGATGGGGTTCCACC[A/G]TGTTGGCCAGGATGG | 10055 |
| rs534823318 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47205816 | TTATAAAAGAGAGAC[A/T]AAGGTGCAGGAAAGA | 10055 |
| rs534903178 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47177395 | ACAGGGTCTTGCTCT[C/G]CTTTCCAGGCTGGAG | 10055 |
| rs535059363 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47205166 | TTATGGAGCAGAGTC[A/G]TGCCTGGTTAAATGA | 10055 |
| rs535118654 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47173219 | GGCCAGGCTGGTCTC[A/G]AACTCTTGACCTCGT | 10055 |
| rs535118789 | snp | C/G | | | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210917 | CTGGATTGATAAAAA[C/G]AAAATTGTAGAATCG | 10055 |
| rs535200592 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47137767 | GGACTCTCACTCTGT[C/T]GCCCAGGCTGGAGTG | 10055 |
| rs535230794 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant, intron-variant | SAE1 | GRCh38.p7 | 19:47131017 | CCTGTGGGGACTGGA[A/G]GCCCAGAAACGGTCA | 10055 |
| rs535236164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47144104 | TTTGGAAGGCTGAGG[C/T]AGGCGGATCATCTGA | 10055 |
| rs535238867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47136970 | TTCCTTTATGAAACA[A/G]AAGCCCTGGAAATGG | 10055 |
| rs535241393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47144917 | GCACACTGCAACCTC[C/T]GCTTCCCGGGCTCAA | 10055 |
| rs535298094 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47151926 | GCAGGTTTTATAGTT[A/T]CTTTAGACTCTGCAG | 10055 |
| rs535299372 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SAE1 | GRCh38.p7 | 19:47184502 | TGCAACCTCCACCTC[C/T]TGGGTTCAAGCGATT | 10055 |
| rs535371136 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47151065 | AAATGTGAAATAGTC[A/T]TAGATGAGCTACTAG | 10055 |
| rs535427231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47165278 | TATTTTTAGTGGAGA[C/T]GGGGTTTCACCATGT | 10055 |
| rs535428640 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47158260 | CAAAAAGGAAAAACA[A/G]CCTGTGGTTTTCACA | 10055 |
| rs535451037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47132496 | CTCCCAAGCTCAAGC[A/G]ATCCTCGGCCTCAAG | 10055 |
| rs535464487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47164860 | GGTTTCACCGTGTTA[A/G]CCAGGATGGTCTCGA | 10055 |
| rs535503540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47171480 | TTTTTTTTTGAGATG[A/G]AGTCTCACTCTGTTG | 10055 |
| rs535531592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47131509 | GCTCACGGGCGGGCC[A/G]GTCTGAGAGAATGCG | 10055 |
| rs535618408 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47152410 | AAAATGATCTCAACA[A/G]GACTTGTTTATCTTC | 10055 |
| rs535634357 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47159927 | TCGAACTCCTGGCCT[C/T]AAGTGATCCGCCCAC | 10055 |
| rs535636307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47167536 | TGAGCCACTGCGCCC[A/G]GCCAACAATTTGAAC | 10055 |
| rs535655556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47158713 | TGTGTGCAAGGCACT[A/G]TGTTGAGTGCAGGGA | 10055 |
| rs535672479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47167196 | TGACCTCTAGTGATC[C/T]ACCCGCCTTGGCCTC | 10055 |
| rs535695378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47192595 | TAGCCCAGACTGGAG[C/T]GCAGCGGTGTGATTT | 10055 |
| rs535702065 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47175585 | CTACTAAAAAACACA[A/G]AAATTAGCCAGGCAT | 10055 |
| rs535758791 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47208291 | TTGAGACAGGGTCTC[A/C]CTCTGTTCCCCAGGC | 10055 |
| rs535836903 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | SAE1 | GRCh38.p7 | 19:47176127 | AACTGTGAAACACCG[G/T]TTGGGAACTTGCTTG | 10055 |
| rs535899507 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, missense | SAE1 | GRCh38.p7 | 19:47205119 | GTTCTTGGCTGCCTT[C/T]GTGGACTCCGGTGAG | 10055 |
| rs535946028 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47201923 | CAGATGTGAGCCACC[A/G]CACCCAGCCCTAGTT | 10055 |
| rs535962448 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47193258 | TAGAGATGGGGTTTC[A/G]CTGTGTTGGCCAGGC | 10055 |
| rs536072453 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47140031 | CAACCTCCGCCTCCC[A/G]GGTTCAAGCGATTCT | 10055 |
| rs536088075 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47160830 | CACCACTCCTGGCCA[A/G/T]TCCTGCTAATTATTA | 10055 |
| rs536112118 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47188903 | AACTGTGGAGGGCCT[C/G]GTCACTTGACAAGGC | 10055 |
| rs536150277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47188281 | ACTTGAGTTCAGGAG[A/G]TCCAGGCAGCAATGA | 10055 |
| rs536163847 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47195659 | CTCTCTTCTAGGTCC[C/T]TTCCCCTTTCCCTTT | 10055 |
| rs536185213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47147958 | GTAGAGATGGGGTTT[C/T]ACCGTATTAGCCAGG | 10055 |
| rs536214629 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | SAE1 | GRCh38.p7 | 19:47147306 | TAACTTCCTGGGCTC[A/C]GGGTATTCTCCCACT | 10055 |
| rs536310847 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47175026 | GAGAACATTTACAAT[C/T]ACATATTGTGTAGCA | 10055 |
| rs536331687 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209900 | AGCTGGGTTTTGGGA[A/G]AAAGGAGATGCTACC | 10055 |
| rs536406437 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47134518 | ATAGGTGGACTGCAT[C/T]GATTTTAGGGACTGC | 10055 |
| rs536416062 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47149623 | AGCAGTTACAAATTT[G/T]CATAGAAGAAGAAAG | 10055 |
| rs536418520 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137616 | GATTCTCCCGCCTCA[A/G]CCCCCAAGTAGCTGG | 10055 |
| rs536418748 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47195214 | TGCCTGCCACCACGC[C/T]TGGCTAATTTTTGTA | 10055 |
| rs536543474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47141494 | GAGCTATGTAGGAAT[A/G]TAGGTCGTGGAGAGC | 10055 |
| rs536551034 | in-del | -/AGT | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47146136 | GAAATGGAAGCTAAA[-/AGT]AGTTTGGTGTTTTTA | 10055 |
| rs536562378 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47204765 | CCTCCCAAAGTGCTG[C/G]GATTATAGGTGTGAG | 10055 |
| rs536565407 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47156378 | CAGCTACTTGGGAGG[C/T]TGAGGCAGGAGAATA | 10055 |
| rs536636805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176621 | AGGCTTTTGATTCCA[A/G]TGTTGCCCTGGGCTC | 10055 |
| rs536675189 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47148986 | TTTGCACAAGTTTGA[-/T]TTTTTTTTTAAGTTT | 10055 |
| rs536713749 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47168332 | TTTCTCTCTCTCTCT[C/G]TTTTTTCTGTCACCC | 10055 |
| rs536740500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47136051 | TCGTGTACCACAATT[C/T]CTTTATCCATTTGTC | 10055 |
| rs536757166 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47169489 | GACCTCATGTGATCC[A/G]CCTGCCTCGGTCTCC | 10055 |
| rs536759698 | in-del | -/A | 0.283421 | 0.247756 | intron-variant | SAE1 | GRCh38.p7 | 19:47132890 | GTGAGGCCCCGTCTC[-/A]AAAAAAAAAAAAAAA | 10055 |
| rs536764826 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47140820 | AAACGTAAACATGGT[A/G]TTTGGTGTTGATGGC | 10055 |
| rs536776181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47143064 | AGAGCCTGTCTCTTT[C/T]CTAGATTCGAGGTGT | 10055 |
| rs536835962 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47156894 | GAGATGGGAACCATG[A/C]GATGGGGAAAGCAAG | 10055 |
| rs536861910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47148914 | CCACCGCACCTGGCC[A/G]TAGTCTATCTATGTT | 10055 |
| rs536869582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47164138 | AAGCATTCCCCAAAT[C/T]TGCTTTGGAGCACAT | 10055 |
| rs536877847 | in-del | -/T | 0.0138799 | 0.0821421 | intron-variant | SAE1 | GRCh38.p7 | 19:47158867 | AGGCTCACCCTATGA[-/T]TTTACAAAGAGGGAT | 10055 |
| rs536886270 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47197108 | ATCACTTGAACCCGG[G/T]AGGCAGAGGTTGCAG | 10055 |
| rs536905696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47170361 | CTGGGATGACAGGCA[C/T]GCACCACTGCGCCCG | 10055 |
| rs536931725 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SAE1 | GRCh38.p7 | 19:47204236 | GGAGTCTCGCTCTGT[C/T]CCCCAGGCTGGAGTG | 10055 |
| rs536967772 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130383 | AAAAAAAAAAAAAAA[A/G]TTGACAGTTCAATGT | 10055 |
| rs537023447 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47144253 | GCACAAGAATCGCTT[A/G]AATCTGGGAGGTGGA | 10055 |
| rs537060642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47151137 | GAATTTGGGTTGGGT[A/G]GTTTTTTTTTTTTGC | 10055 |
| rs537077883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47184144 | AATATTGGGCTGGGG[C/T]TAGTCTGAAATGGTG | 10055 |
| rs537087389 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47186233 | AACAGAGAGAGACTC[-/T]TGTCTCAAAAATAAA | 10055 |
| rs537112156 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47183279 | GCCTTACTAGATCAG[C/G]TCTTGTCCTGTTTTC | 10055 |
| rs537196597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47157550 | ACAGCTGGAAGTTTC[C/T]CTGGAGTCAGTTCTG | 10055 |
| rs537244001 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47172030 | TTCAAACAGTTTCCC[C/T]GCCTCAGCCTCCCGA | 10055 |
| rs537244661 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47178746 | CCAGGTGCTGAGTTT[A/T]TAGGCATGAGCCATC | 10055 |
| rs537280401 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47178142 | GCTACTCGGGAGGGG[A/G]AGGCAGGAGAATCGC | 10055 |
| rs537286781 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47206010 | TGTCAGCCTTACTTC[C/T]GCACATCCCATTGAG | 10055 |
| rs537354053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47185387 | TCGGCTCACTGCGAC[C/T]TCCACCTCCCAGGTT | 10055 |
| rs537490663 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47201433 | CTGGAGTGCAGTGGC[A/G]TGATCTCGGCTTATT | 10055 |
| rs537494642 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47208363 | GTCCCAGGCTCAAGC[G/T]ATCCTCCCACCTCAG | 10055 |
| rs537503879 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47165309 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 10055 |
| rs537525846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47206698 | TTTGAGGGTCTAAGA[A/G]TTCCACCTGTGTACT | 10055 |
| rs537596976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47131849 | GGGATTATAGGGGCC[C/T]GCCAGCACGCCCGGC | 10055 |
| rs537599832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47150685 | TTCCAGAATCTTTGC[A/G]CATAACTTTAATCCA | 10055 |
| rs537728115 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47183149 | TCAAACTCTTGACCT[C/T]AGGTGATCCACCCAC | 10055 |
| rs537729069 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47208889 | AGATACATAGTTTAA[C/G]CCAGGCAAATACATT | 10055 |
| rs537729861 | snp | C/T | 0.000951701 | 0.0217932 | intron-variant, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47131086 | GCGTCTATTCTGAGG[C/T]GTTTGCGGCCCGGAA | 10055 |
| rs537732735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47200616 | TGGATTCAAGCCATC[C/T]TTCTGCCTTGGCTTT | 10055 |
| rs537755981 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47192493 | ACCTCGTGATCCACC[C/T]GCCTTGGCCTCCCAA | 10055 |
| rs537767859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47201511 | GGAGTAGCTGGGACT[A/G]TAGGCACGTGCCACC | 10055 |
| rs537768736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47137980 | GTGATCTGCCCACCT[C/T]GGCCTCCCAAAGTGC | 10055 |
| rs537782633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47144653 | GCAACGAGCCGAGAT[C/T]ATGCCACTGCACTCC | 10055 |
| rs537800228 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47133854 | TAGGTTTCAGATTTG[G/T]TTTTTTTGTTTGTTT | 10055 |
| rs537840794 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SAE1 | GRCh38.p7 | 19:47167274 | CCAGATAATTTTTGT[A/G]TTTTTTTTTTTTTTG | 10055 |
| rs537905027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47172463 | TCAGGAAACAATGGC[A/G]CTAATTTGCCAAGGT | 10055 |
| rs538017560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47146295 | TTTCAAATGACAGGA[A/G]GGGTGACATGGTTAG | 10055 |
| rs538020690 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47138280 | AACTCCTGACCTCAG[A/G]TGATCTACCCGCCTC | 10055 |
| rs538025304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47154265 | CCGGCAAATTTTTGT[A/G]TTTTTAGCAGAGACG | 10055 |
| rs538078721 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47168222 | TAAAACAAAAAACTG[G/T]TTTTTTGTATGTGTG | 10055 |
| rs538083905 | snp | A/G | | | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47169894 | AGGCTGCTCTGAAGC[A/G]CACGACCTCCGACTA | 10055 |
| rs538191449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47152487 | TATTTAAACATGACC[C/T]TTGGGTCAATTTAAA | 10055 |
| rs538220593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47148776 | TGTGCCACCACGTCC[A/G]GCTAATTTTGTATTT | 10055 |
| rs538271226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47180670 | TCTACAAAAAATAAA[A/G]AAGTTAGCCAGATAC | 10055 |
| rs538272861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47173116 | TCACTGCAACTTCTG[C/T]CTCCTGGGTTCGAGC | 10055 |
| rs538295246 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47136525 | TTTGAGACGGAGTTT[C/T]GCTCTTGTTACCCAG | 10055 |
| rs538364292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47140199 | GCAAACTCCACCTCC[C/T]GGGTTCACGCCATTC | 10055 |
| rs538370286 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47194934 | TTTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 10055 |
| rs538396069 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47154827 | TTCATGATTCAAGTA[A/G]AGTGTTTACAAAGTA | 10055 |
| rs538408164 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47172675 | AAAGCACTCCAGCCT[A/G]GGTGACAGAGCTGAA | 10055 |
| rs538437229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47175692 | CAGTGAGCCGAGATC[A/G]TGCCACTGCACTCCA | 10055 |
| rs538447845 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47160541 | CTGGGACTACAGATG[A/C]CCGCCGCCATGCCCG | 10055 |
| rs538476643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47174850 | AGTGCTGGGATTACA[A/G]GCGTGAGCCACCGCG | 10055 |
| rs538484190 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47167631 | CTTGGTTCACTTAGC[A/T]TCCCAAATTATGCTG | 10055 |
| rs538486990 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210654 | CTGCAGCAGTTAGTC[A/G]GGGAGAAAAGTGGTC | 10055 |
| rs538544554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47135323 | CCCTCCTTCCCCTCC[A/G]CCCCCCACTACCCTT | 10055 |
| rs538549024 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209966 | AGTATTAGAGAGCTT[C/G]TCTTTCAAGGCAGGT | 10055 |
| rs538560814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47189921 | CGTTATAGCGCTAAC[C/T]TGATGTTATGAACTG | 10055 |
| rs538582617 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47142316 | TTGGACCTGGGAGGC[C/G]GAGGTTGTAGTGAGC | 10055 |
| rs538611617 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129960 | TAGCTGGGACTACAA[A/G]TGTGAGCCACCATGC | 10055 |
| rs538649912 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47136173 | AGACCGAGCCTCGCT[C/T]TGTTGCCCAGGCTAG | 10055 |
| rs538670091 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47189106 | TTTATTGAATGAACA[A/C]TTGACTGAATGTCAG | 10055 |
| rs538671422 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SAE1 | GRCh38.p7 | 19:47163001 | TGTCTCAAAAAAAAA[A/T]TTTTTTTTAAGTAAA | 10055 |
| rs538694599 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47204902 | CTGTACAGGATGACC[A/C]GTGACCCTGTTAGGT | 10055 |
| rs538695438 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47155963 | CCAGGATGGTATTTA[G/T]CTCTTGACCTCGTGG | 10055 |
| rs538701400 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47165244 | ACAGGCACATGCCAC[C/T]ATGTCCGGCTAATTT | 10055 |
| rs538706215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47195766 | TTTTTGACAGGGTCT[C/T]ACTCTGTCACCCAGG | 10055 |
| rs538712109 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47169761 | GAGAAGAGCAACTGC[C/T]TTGTGATTGGAAGCC | 10055 |
| rs538713720 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47144657 | CGAGCCGAGATCATG[A/C]CACTGCACTCCAGCC | 10055 |
| rs538803287 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47151206 | CCAGGCTGGAGTGCA[A/G]TTGTGCGATCTTGGC | 10055 |
| rs538810623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47185972 | GCCCCGGGCGTGGTG[A/G]CTCATGCCTGTAATC | 10055 |
| rs538816570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47169235 | GTATGAATACAGCCA[A/G]AGGTTTTTTAGTTTT | 10055 |
| rs538828075 | in-del | -/TTTC | 0.00199601 | 0.0315281 | intron-variant | SAE1 | GRCh38.p7 | 19:47151463 | CCTGTTTTTTACACT[-/TTTC]TTTCTTTCTTTCTTT | 10055 |
| rs538903002 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191615 | GATGGACAGTGGCAG[C/G]AACCCTGTGCTAGAT | 10055 |
| rs538933526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47205638 | GTTCTAAGTGGGGAA[C/T]GGGAATGTACATATT | 10055 |
| rs538950543 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47134617 | TCTGAGATCCTAAAG[G/T]GTTGGGGAGGGGATT | 10055 |
| rs538968622 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47197854 | CGTACGTGTGCAGGT[A/G]CAACTGCAGGATAAT | 10055 |
| rs538988005 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SAE1 | GRCh38.p7 | 19:47206987 | TGAATACCTGGCATA[A/G]AGTAGATGCTTAATA | 10055 |
| rs538997359 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, missense, intron-variant | SAE1 | GRCh38.p7 | 19:47130928 | GCAGGAAGAGCCGGC[A/G]CCATGGTGGAGAAGG | 10055 |
| rs539006063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47162540 | TTTGATTATGGTTGT[C/T]ATTTGTTAGAATACT | 10055 |
| rs539047102 | in-del | -/TG | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47176115 | TTTATGTAATCAAAC[-/TG]TGAAACACCGGTTGG | 10055 |
| rs539093530 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47193384 | CAGCTTTGAGTTGAC[C/T]GCCAAGTGTTGAGGT | 10055 |
| rs539146156 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130504 | TTTATATTTATTTCT[C/T]TTCGGGCTTTTCTCA | 10055 |
| rs539161293 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47184285 | ACACTATAACGTAGA[C/G]GTTAAGAATGTGGTG | 10055 |
| rs539195408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47136879 | GGCTCCACAGAGCAA[A/G]TTGACTTGCCTCTAA | 10055 |
| rs539236012 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47150460 | AATCCCAAAGCAATC[G/T]GAGAGCATTCAAATA | 10055 |
| rs539270098 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47157719 | CCTACGTGGAGCTGA[G/T]CTGGAAGGTATCAAA | 10055 |
| rs539305630 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SAE1 | GRCh38.p7 | 19:47164497 | TAAATGTCTGTGTCA[C/T]TTTTCCTCTTCTTGC | 10055 |
| rs539411495 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47145410 | CCTCGGCCTCCCAAA[G/T]TGCGGTGATTACAGG | 10055 |
| rs539423425 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47138371 | CTTTGTGCCTGTTTT[C/G]TCAGCTGCAAAAGAG | 10055 |
| rs539433188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47171300 | TTAATTTTTATTTTA[A/G]TTTTTTTTTTGGAGA | 10055 |
| rs539450269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47144850 | GTTTGTGTGTTTTTG[C/T]GAGACGAGTCTTGCT | 10055 |
| rs539486730 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | SAE1 | GRCh38.p7 | 19:47186079 | ACCCCGTCTCTACTA[A/C]AAATACAAAAATTGA | 10055 |
| rs539525287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47192542 | ATCAGCCACCATGCC[C/T]GGCTACTTAATTTAT | 10055 |
| rs539585155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47151893 | GACCGCCTTGCAGGC[C/T]GTGTTTGGCTGGTCC | 10055 |
| rs539594573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47158118 | CAGCTACTTCCTGTT[C/T]CCTGTGAAAGGTTTT | 10055 |
| rs539607580 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47207941 | AAGCCCAGCCCTGTT[A/C]TTGTATTTTAAAGTG | 10055 |
| rs539633016 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47165209 | ATTCTCCTGTCTCAG[C/T]CTCCCAAGTAGCTGG | 10055 |
| rs539637867 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47166302 | CAGCTTTCCCGATGT[G/T]CCTTAATCTGGCACA | 10055 |
| rs539693371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47198849 | CCAGCACTTTGGGAG[A/G]TTGAGGCAGGCAGAT | 10055 |
| rs539705957 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47140349 | CTGACCTCGTGATCT[A/G]CCTGTCTCGGCCTCC | 10055 |
| rs539755851 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47206731 | TGGACCCTTCCACCT[C/G]GCTAGGTTGGTGGCA | 10055 |
| rs539856972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47194477 | ACGGAAGAGATATCA[A/G]TGAAAGAACTGACAA | 10055 |
| rs539881265 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SAE1 | GRCh38.p7 | 19:47193126 | GCAGTGGCACAATCT[C/T]GGCTCACTGCAACCT | 10055 |
| rs539890467 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47193431 | GAAGCTGTGTTCTTG[A/G]AAAAGAGAAGAGAGT | 10055 |
| rs539916920 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47199946 | TGGCTTTTTTTTTTT[G/T]TGGAGACAGAGTCTC | 10055 |
| rs539926576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47192764 | AGGCTGGTCTCAAAC[C/T]CCTGACCTCAAGTGA | 10055 |
| rs539926972 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47199685 | ATGCTCAGTGGCTGC[C/G/T]GCTTGCCACTGGCTG | 10055 |
| rs539952725 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47200764 | TCATTTATATATTAT[C/G]TGTGGCAGCTTTTGT | 10055 |
| rs540026705 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47133111 | AGGCATGATTGTCAA[A/C]TTAGAGAAATAAGGT | 10055 |
| rs540093726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47180014 | GTGGACAGTGGGAAA[A/G]GCTAGAAGGAGCCAT | 10055 |
| rs540126192 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47132430 | CTAATTTTTGTTTTT[G/T]TTTTTTTTTGTAGGA | 10055 |
| rs540250206 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47145182 | TAATTTAACGTTTTT[A/C]GTAGAGACCGGGTTT | 10055 |
| rs540256682 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SAE1 | GRCh38.p7 | 19:47160546 | ACTACAGATGCCCGC[C/T]GCCATGCCCGACTAA | 10055 |
| rs540275341 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47142772 | TGTGTTTGTCCTTTA[C/T]TTCATTTTGATTTTT | 10055 |
| rs540308788 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47210026 | GCCTGCCCTTTTAAC[A/G]GAACCCCAGTCACAT | 10055 |
| rs540409261 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47141192 | TTTTCTGTAGAGACA[A/C]GGTTTTGCCATGTTA | 10055 |
| rs540443999 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47147717 | CTCAGCCTCCCAAGC[G/T]GCTGGGTTTACAGGT | 10055 |
| rs540468293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47172846 | TTGCTCTGTGCCGGG[C/T]GTTTTCCATGTATAT | 10055 |
| rs540481158 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47146820 | AGGCTTCTGGCTTGA[A/G]TGACTGGGTGGGTGG | 10055 |
| rs540493768 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47179170 | GCACTCCAGCATGGG[A/C]GACAGAACAAGGCTC | 10055 |
| rs540532483 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47186771 | AGACTGGGTTTCATT[A/G]CAAAGACGAAAGCGT | 10055 |
| rs540567351 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47139652 | GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC | 10055 |
| rs540615275 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47153363 | TCCAGAGAGACTCCT[C/G]TGGTAGAACAAACAG | 10055 |
| rs540636220 | in-del | -/GAA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163265 | CCAAAAAAAAAAAAA[-/GAA]AATTGAAATTATGTT | 10055 |
| rs540679400 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47134884 | AGTGGAGCTGTACCA[A/C]ATTTGGTGGAGAACA | 10055 |
| rs540698845 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47173975 | ATTTTTAGTAGAGAC[A/G/T]GGGTTTCACCGCGTT | 10055 |
| rs540705915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47174714 | AGTAGCTGGGACTAC[A/G]GGTGCCCGCCACCAT | 10055 |
| rs540722786 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209469 | GTCTTTGTTCCAGCA[C/T]TGTTCAGGCTGCCTG | 10055 |
| rs540816084 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47166922 | AAAGGAAAGCCACCT[A/G]AACATGACTGTTTAA | 10055 |
| rs540860076 | in-del | -/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137727 | TGTGTGTGTGTGTGT[-/G]TTGTTTTTTTTTTTT | 10055 |
| rs540898302 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163846 | GCTGGAGCGCAGTGG[C/T]GTGATCTCCGTCTCC | 10055 |
| rs540914222 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47194964 | TGGCCAGGCTGGTCT[C/G]TAACTTCTGACCTCG | 10055 |
| rs540949384 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SAE1 | GRCh38.p7 | 19:47194640 | AGACTGGCTGTGCCC[G/T]TTCCTTGGGCAGTAT | 10055 |
| rs541073576 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47191163 | TGCCTATAATCCCAG[C/T]ACTTTGGGAGGCTGA | 10055 |
| rs541100069 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47148725 | GTTCAAGCGATTCTC[C/T]TGCCTCAGCCTCCCG | 10055 |
| rs541105860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47196966 | GGCGGGCGGATCACG[A/G]GGTCAGGAGTTTGAG | 10055 |
| rs541110243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190532 | AGTGAAAAAAGACAG[C/T]TTCTGTTTGTTTTGC | 10055 |
| rs541133535 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47181009 | TTTGCTCTAAAGGAT[C/G]TTAGTGGAACAATTG | 10055 |
| rs541164449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47134318 | TTAGTTTGAGGGGGT[A/G]GGAGCTTTCAGAAGG | 10055 |
| rs541191954 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47187549 | TTTTTCTGAGCCAGG[G/T]TCTCGCTTTGTCACC | 10055 |
| rs541212600 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47138560 | GACACAGGTTTGTTT[C/T]GGTGTGTCTATTAAT | 10055 |
| rs541213026 | in-del | -/AA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47179816 | GTGAGCCTCCTGCCC[-/AA]AGTGTTGGGATTACA | 10055 |
| rs541240774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47155059 | AGGCTTTTTTTGATT[C/T]CAATAACATGATTCC | 10055 |
| rs541259295 | snp | A/G | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47191240 | ACATAGTGAAGCCCC[A/G]TCACTAGTAAAAATA | 10055 |
| rs541275983 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47141649 | TGGGTTTTGAAGGGG[A/G]AAGGCGTAGGTAGGC | 10055 |
| rs541307693 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47177746 | CTTAGGAAACTGAAG[A/G]TCTGACCATCTTTGG | 10055 |
| rs541322470 | snp | A/C | 1.64817e-05 | 0.00287064 | intron-variant | SAE1 | GRCh38.p7 | 19:47203623 | CCAGATGTCATGGTC[A/C]CAGTTCTGTTCCCAG | 10055 |
| rs541370866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47183634 | GCAGGCCCACATCTC[C/T]CCCACTCCCCCACCC | 10055 |
| rs541384453 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47135763 | GCTGGGATTAGAGGC[A/G]TGAACAGCAATGCCC | 10055 |
| rs541400612 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47171001 | TTGTTTTTGAGATGG[A/G]GTCTCGCTCTGTCCC | 10055 |
| rs541433495 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47149915 | ACCCTGTCTCTACTA[A/C]AAATACAAAAATTAG | 10055 |
| rs541442836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47142804 | CTCATATGGCATCTC[C/T]TCAGAAAGGCTTGTA | 10055 |
| rs541444372 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47150825 | AGAAAAGCACACCTG[A/T]TCTTGATCTATGTCT | 10055 |
| rs541460337 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47182677 | TGAGAGAACAGAACT[C/G]GTTAGTCACCGACTC | 10055 |
| rs541498457 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167781 | AACCTTTTTAAAATA[C/T]AGAGACACAGAGTCT | 10055 |
| rs541501306 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47130842 | GCAGAAGCACTCCGG[A/G]CGTGCTGCCGGCGGC | 10055 |
| rs541503490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47198274 | GCCACCACGCCCAGC[C/T]AATTTTTTTTGTATT | 10055 |
| rs541566723 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47206163 | CTGGAGACAGCTGGT[G/T]CCCAGCATCTTGTTT | 10055 |
| rs541592398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47138087 | TCTCTCTTGTTGCCC[A/G]GGCTGGAGTGCAATG | 10055 |
| rs541601344 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SAE1 | GRCh38.p7 | 19:47207836 | ATATGGGGTTTTGCC[A/G]TGTTGCCCAGGCTGG | 10055 |
| rs541630413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47144379 | AGGAGATTATGATTT[A/G]GATGGTCCACAGACA | 10055 |
| rs541635254 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47198738 | GCAACAGCAAACCCC[A/G]CTCCATTTAGGGCCA | 10055 |
| rs541637242 | in-del | -/ACT | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47163088 | TACTACCAAATGATA[-/ACT]ACTATAACCTTCCTT | 10055 |
| rs541638349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47163774 | GATGCACGTAGAGTA[C/T]ATGCAAGTACTGTGC | 10055 |
| rs541682470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47169993 | AAATGTGGTTGCAAG[A/G]TCCAGATGGTTTTGT | 10055 |
| rs541746643 | in-del | -/AA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47150075 | AGCAAGACTGTCTCA[-/AA]AAAAAAAAAAAAAAA | 10055 |
| rs541820538 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47165675 | TAATGCCAGTGGAGT[G/T]GGTAAGACAGGTACC | 10055 |
| rs541964963 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47177551 | CTGTTTGTACAGATT[A/G]GGGCAGGGAGGTCTT | 10055 |
| rs542081386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47152155 | TGTGCAATTTGGAAG[C/T]TGTCTTTTGACCATG | 10055 |
| rs542086599 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47198939 | AAAAAATAGAAAAAT[G/T]AACTGGGCATCGATG | 10055 |
| rs542091391 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47185596 | CAGGCTGAGCTACTG[C/T]GCCCAGCCTATTTTT | 10055 |
| rs542128031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47192255 | GTTGTTGTTGTTGTC[A/G]TCGTTGTTGTTTTGA | 10055 |
| rs542151794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47151384 | TTGAACCCCTGACCT[C/T]AGGTAATCCACCTGC | 10055 |
| rs542164900 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191794 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 10055 |
| rs542165846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47200075 | AGCTGGGATAACAGG[C/T]GCCCGCCACCACGCC | 10055 |
| rs542240718 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47172132 | CCATGTTGGCCAGGC[C/T]GGCCTCAAACTCCCA | 10055 |
| rs542242028 | in-del | -/TTTG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47208255 | GTTTTAAGGTGTTTT[-/TTTG]TTTGTTTGTTTTTTG | 10055 |
| rs542259056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47187526 | CAGGAGCTTGTGTCA[C/T]TTTATTTTTTTTCTG | 10055 |
| rs542297637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47186798 | GCGTGGGCAGGACTT[C/T]TGGAGCACAAAAAGG | 10055 |
| rs542332589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47193712 | GGCACCTGTAATCCC[C/T]AGTTACTTGGCAGGT | 10055 |
| rs542392257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47152691 | GGCTGCAGAACGTGA[C/T]GGTCTCATAACTTAT | 10055 |
| rs542447095 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209631 | CAAGCTCTGTTGCTC[A/G]GGAGCCTCTTGTCAC | 10055 |
| rs542461760 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47133585 | TCAGAAATGGAAGTA[A/C]AGATTCTGGCTGGAC | 10055 |
| rs542488979 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47173817 | TGAGACGGAGTCTCT[C/T]TCTGTCACCCAGGCT | 10055 |
| rs542699816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47203545 | AGCATTAACACTGCT[A/G]TCTGAATCGGGCCCT | 10055 |
| rs542754350 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47145749 | TCTGGTTGTAAGAAT[A/C]CAACATTGGAGGCCA | 10055 |
| rs542843238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47167862 | GTTCCCCCAGCTTGG[C/T]TATCTTAAACTTCTT | 10055 |
| rs542843394 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47160290 | GCAATGGTGCGATCT[C/T]GGCTCACTGCAACCT | 10055 |
| rs542878999 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47173195 | GTAGAGGCAGGGTTC[C/G]ACCGTGTTGGCCAGG | 10055 |
| rs542889960 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163419 | AGGTATTATAAGTAA[C/T]CTAGAGATGATTTAA | 10055 |
| rs542942114 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47143183 | TGATCTCGGCTCACT[A/G]CAACCTCCGCCTCAT | 10055 |
| rs542954345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47141296 | CGTGAGCCCCCACGC[C/T]TGGCCATAATTTTTT | 10055 |
| rs543029359 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47154966 | CTCATCATGTTATCA[A/G]TGGCAGAGCTCGATT | 10055 |
| rs543030404 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SAE1 | GRCh38.p7 | 19:47154481 | AGAATTAAGTTTGGC[C/T]TTTTTTTTTTTTTTT | 10055 |
| rs543086063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47169358 | TCAAGCGATTCTCCT[A/G]CCTCAGCCTCCCAAG | 10055 |
| rs543106904 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SAE1 | GRCh38.p7 | 19:47160597 | AGATGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 10055 |
| rs543107408 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47128975 | ATGCGCCTGCCACCA[C/T]GCCCGGCTAATTTTT | 10055 |
| rs543114500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47202864 | GCAGTAAGCCAAGAT[C/T]GCGCCACTGCACTCC | 10055 |
| rs543142060 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47135546 | GGGTCTCTCTGTCGC[G/T]CAGACTAGAGTGCAG | 10055 |
| rs543220723 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47194153 | CTTCACAGATGCAGA[C/G]ACCAAGATTCACTCA | 10055 |
| rs543273385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47163557 | ACATGGTGAAACCCC[A/G]TCTCTAACAGAAATA | 10055 |
| rs543275269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47155705 | CCTCAGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 10055 |
| rs543285967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47181899 | GCCTCAGCCTCCTGG[A/G]CTCAAGCGATCCTCC | 10055 |
| rs543294807 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47135421 | ACAAATAAGTGACAG[C/T]GTGCAAAGTTTTCTT | 10055 |
| rs543452657 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47176334 | ATTGTTTCTAGGAAC[A/G]TGACTAATGTGACTG | 10055 |
| rs543454656 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47184657 | CTCAGGTGATCCACC[A/C]ACCTCAGCCTCCCAA | 10055 |
| rs543461609 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47138040 | GGCCTATGTGTGTGT[A/G]TTTTATTTTTTTATT | 10055 |
| rs543476921 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47180694 | CAGATACAGTGGTGC[A/G]TGCATGTAGTCCTAG | 10055 |
| rs543477439 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47168523 | GTTATTTGACTCCTG[A/G]ACTCAGGTGATCATG | 10055 |
| rs543600867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47143305 | AGACGGGGTTTCACC[A/G]TGTTGGTCAGGCTGG | 10055 |
| rs543644489 | snp | A/G | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176698 | ACCTGCTGTCCGCAT[A/G]CATGTGCTTGCCATG | 10055 |
| rs543683832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47164368 | AGAGACGGGTTTCAC[C/T]GTGTTAGCTAGGATG | 10055 |
| rs543689048 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47152812 | AGCATGCCCAGAGAG[A/T]CTGTTCATTAAGATT | 10055 |
| rs543709554 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47197068 | TGCCTGTAGTCCTAG[C/G]TACTCAGGAGGCTGA | 10055 |
| rs543723532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47170696 | ATTTTTTTGTAGAAG[C/T]GAAGTTTCTCCATGT | 10055 |
| rs543748935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense | SAE1 | GRCh38.p7 | 19:47205128 | TGCCTTCGTGGACTC[C/T]GGTGAGGCTTTTTCC | 10055 |
| rs543803200 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47137129 | TCACAGTGACTCAGC[C/G]TGTAATCCCAGGACT | 10055 |
| rs543808907 | snp | C/G/T | 3.32813e-05 | 0.00407919 | intron-variant | SAE1 | GRCh38.p7 | 19:47143651 | CTCTGGCTCCCCTTT[C/G/T]CAGCATGAAGATCTG | 10055 |
| rs543837004 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47147028 | GCATTGAGTTGGTTT[A/G]TGGAGCTATACAGAG | 10055 |
| rs543841230 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47136262 | TCCTGCCTAAGCCTC[A/C]CAAGTAGCTGAGATT | 10055 |
| rs543841804 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47198112 | TCACAATCTCTCTCT[C/T]TCTTTTTTTTTTTTG | 10055 |
| rs543851525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47144495 | ATGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 10055 |
| rs543879097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191771 | AACATAGCTGTGGGA[A/G]TAGGCCGGGCGCGGT | 10055 |
| rs543916288 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167026 | GTGTGACCTTGGCTC[A/G]CTGCAACCTCCACCT | 10055 |
| rs543966533 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47132072 | GGTTCAAGACTTCCT[C/G]TCACCTCAGTCTTCT | 10055 |
| rs543980639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47199121 | GCTGGGCGCGGTGGC[C/T]CACGCCTGTAATCCC | 10055 |
| rs544020394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47157224 | CTAATTTTAGTGTCT[A/G]TTCACAGAACCATAA | 10055 |
| rs544023224 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47171512 | CCAGGAGAGCAGTGG[C/T]GTGATCTTGGCTCAC | 10055 |
| rs544212643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47152034 | GCATTCTTTGAAACA[C/T]CAAAGGAACACATTT | 10055 |
| rs544242834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47199898 | GCTGATGTTACAAAG[A/G]CACCTTGTAAACTGC | 10055 |
| rs544263285 | in-del | -/GT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47195186 | CAGCCTCCTGACTAA[-/GT]GGGACTACAGGTGCC | 10055 |
| rs544276336 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47157817 | AAGCCCTTAAGGTTA[C/G]GAGGCATTCAGTGCA | 10055 |
| rs544325730 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47132530 | TCTCCCCCCATCTCA[C/G]ACTCCTAAAATGCTG | 10055 |
| rs544343366 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47165938 | CTGCATTCCAACTTT[C/T]ACATTTTCAGTTCCC | 10055 |
| rs544397314 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47138681 | GAGGAGGGGGCAGTA[A/T]ACATATAAACAAGTA | 10055 |
| rs544456942 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47160002 | TCCAGCCTGATTGTT[G/T]CCATTTTAAAAAAGA | 10055 |
| rs544462665 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47178495 | TTATTTTATTTTTGA[G/T]ACAGAGTCTAGCTTT | 10055 |
| rs544497353 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47186322 | TGGGGTGCTCTATTG[A/G]TAAGTACAATGCAAA | 10055 |
| rs544534479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47185746 | ACCTGGGATTACAGA[C/T]GTGTGCCACCACACC | 10055 |
| rs544567962 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47193799 | CGCCATTGCACTCCA[G/T]CCTGGGCAACAGAGC | 10055 |
| rs544621585 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47166595 | ATATAGTAGCCTAAC[A/G]TATTAGTTGGTTCGT | 10055 |
| rs544642935 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47173272 | AAAGTGCTGGGATTA[G/T]AGGCGTGAGCCACCG | 10055 |
| rs544647205 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47180899 | CCTCAGCTGAGTGAT[G/T]AAATTAACAATCTAG | 10055 |
| rs544652709 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47208572 | CAGCCTCCCGAGTAG[C/T]ATGCCACCATACTCG | 10055 |
| rs544741445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47147361 | CAGGTGCACGCCACC[A/G]CACCTGGCTAATTTT | 10055 |
| rs544755479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47188391 | CAAACTGTGAGTAAG[A/G]TATCTAAGGGAAAAA | 10055 |
| rs544767387 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47146749 | ACTCCAGAGCCCATG[A/T]TCTCAGCCACCTCAC | 10055 |
| rs544802586 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47210170 | TTTTAAAGGAATGAT[A/G]ATAAAGTTACTTGCT | 10055 |
| rs544841283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47202897 | CCTGGGTGACAGAGC[A/G]AGACTCCGTCTCAAA | 10055 |
| rs544845979 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47170207 | AGATTGAGAAACCTC[-/T]TTTTTTTTCTTTTTT | 10055 |
| rs544892745 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209401 | GAAGGAGGTGGTGCC[A/G]ACGTGCTGCTTCCCA | 10055 |
| rs544894394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47201006 | GGGATTACGGGCATA[C/T]GCCACCATGCCCAGC | 10055 |
| rs544908343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47173887 | CCTCCTGGGTTCACG[C/T]CATTCTCCTGCCTCA | 10055 |
| rs544909568 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47211018 | AGGAATCGAGGGGAA[A/G]GCTGCCAGCCCCAGG | 10055 |
| rs544937419 | snp | C/T | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129759 | TTTTTTTTTTTTTTC[C/T]CTTCCTTCCTTCCTT | 10055 |
| rs544940543 | snp | A/C | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190403 | AAAGGAGAATTTAAT[A/C]AGCGAGAACTTGTCA | 10055 |
| rs544944204 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182700 | ACCGACTCTGCTCCT[C/T]GGTCTGCAAGAGAGG | 10055 |
| rs545048841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47196920 | AGGTGCCGTGGCTCA[C/T]ACCTGTAATCCCAGC | 10055 |
| rs545072924 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47203593 | TTATTCAGGAGAGCC[C/T]ACTACTGAATTTCTC | 10055 |
| rs545086883 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47196208 | CTGGCTAATTTTTTT[A/T]ATATTTTTAGTAGAG | 10055 |
| rs545102972 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47187649 | ACCTCAGCCTCCCAA[A/G]TAGCTGGGACTACAG | 10055 |
| rs545109852 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47204291 | CAAGCTCCACCTCCC[A/G]GGTTCACGCCATTCT | 10055 |
| rs545169153 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129113 | GTGAGCCACCACCTC[C/T]GGCCTAAGCAATTCT | 10055 |
| rs545195669 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47147500 | ACTTGTCGCCCAGGC[C/T]GGAGTGCAGTGGTGA | 10055 |
| rs545208315 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47146196 | GGACAGGTTGCTGGT[C/G]AAGTCCAAGTCAGGA | 10055 |
| rs545212604 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47154536 | CTTTCACTCAGTTGC[C/T]CAGGCTGGAGTACAG | 10055 |
| rs545215243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47160675 | GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCC | 10055 |
| rs545250411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47168010 | CTAGCCTGGGCAATA[C/T]AGTGAAATCCTGTCT | 10055 |
| rs545258908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47178578 | TTTTGGATTCGTGCA[A/G]TTCTCCTGCCTCAGC | 10055 |
| rs545284414 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47135629 | CCCACCTCAGCCTCC[C/T]GGTAGTTGTGACTAT | 10055 |
| rs545336651 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47189406 | ACTAAAAAATATGTA[G/T]ATAAATGAGCCGGGC | 10055 |
| rs545354640 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47182509 | TGTGCGCGCACGCAC[A/G]CGCGCGCGCACACCA | 10055 |
| rs545371499 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47141972 | CTGGTTCAAGAGATT[A/T]CAGATAAGATATAGT | 10055 |
| rs545375767 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47135077 | GTATACATTTTGGGG[A/G]TATGTGAGATACTTT | 10055 |
| rs545396506 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47149080 | TCTTGAGCTCCTGGC[C/T]TCAAGCAGTGATCCT | 10055 |
| rs545401787 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47185390 | GCTCACTGCGACCTC[C/T]ACCTCCCAGGTTCAA | 10055 |
| rs545426448 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47142676 | GTCATTCCTGTCCCT[A/G]GAACATGCCAAGCAC | 10055 |
| rs545433518 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SAE1 | GRCh38.p7 | 19:47148502 | TAATCTTACTGGTGG[A/C]TATTAGGGGATTATA | 10055 |
| rs545438068 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137567 | AGTGACGTGATCTTC[A/G]GCTCACTGCAACCTC | 10055 |
| rs545470613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47155028 | CTTAACCACCATCCC[A/G]ATCTGTGACCTGGAG | 10055 |
| rs545529228 | snp | G/T | 0.00597247 | 0.0543191 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129746 | GGGCCATCCCTGGTT[G/T]TTTTTTTTTTTCCCT | 10055 |
| rs545600557 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47171222 | TCGTGATCCGCCCAC[A/C]TCAGCCCCCCAAAGT | 10055 |
| rs545608813 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47150723 | GCAAATGTTTTCTTC[A/C]GAAAACTTAACAAGT | 10055 |
| rs545624071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47183411 | TCCCCAGGGCCTTGT[A/G]TTTAAGCATCGCCCA | 10055 |
| rs545624443 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47154884 | GTGTGCCCAGCAGTG[A/T]GCTGAGCAACTTACG | 10055 |
| rs545647727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47150082 | ACTGTCTCAAAAAAA[A/G]AAAAAAAAAAAAATT | 10055 |
| rs545654689 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47175400 | TCAGAATTTAGACCA[C/T]GAGGTTTGTTTTACC | 10055 |
| rs545674017 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47202689 | GAGGCCGAGGCGGGC[A/G]GATCACGAGGTCAAG | 10055 |
| rs545712545 | in-del | -/T | 0.0504357 | 0.150579 | intron-variant | SAE1 | GRCh38.p7 | 19:47171904 | TTTTTTAAAAAGTAT[-/T]TTTTTTTAATGTTAT | 10055 |
| rs545771605 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47164208 | AAGTCTCGATCTGTC[A/G]CCCAGGCTGGAGTGC | 10055 |
| rs545834086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47177479 | TCCTCTCACCTCGAC[C/T]TGCAAAGTAGCTGGG | 10055 |
| rs545854084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47205281 | ACATTCTGGAGGCGT[C/T]TGGCTCAATTTGTTA | 10055 |
| rs545855163 | snp | A/G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47173454 | CTTTGCTCCTAGATA[A/G/T]CAGTTTTGTCCCCTC | 10055 |
| rs545872268 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47177945 | TGGTTTCCCTATTGA[A/T]AGAATATCAGAATCT | 10055 |
| rs545876971 | snp | C/T | 1.65537e-05 | 0.0028769 | intron-variant | SAE1 | GRCh38.p7 | 19:47169947 | TCAAAGCACAACTTA[C/T]CCCGGGAGAGCTTTT | 10055 |
| rs545912900 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47197913 | GGTTGTAATTTATCA[C/T]TTGGTCAGCATTGCC | 10055 |
| rs545915622 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SAE1 | GRCh38.p7 | 19:47169439 | TTGTAGAGACGGGGG[A/T]TTCACCATGTTGGCC | 10055 |
| rs545915695 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47175987 | TTTGAAGGCAGAAAA[A/T]GTTTTCTTTGTTAAA | 10055 |
| rs545932551 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SAE1 | GRCh38.p7 | 19:47144306 | ACCACTGCACTCCAG[C/T]CTGGGCAACAGAGTG | 10055 |
| rs545987449 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47206785 | CTGGCCCTATTATTA[C/T]TAATAGCAGCTCCTA | 10055 |
| rs545994922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47184700 | ACAGGCGTGAGCCAC[C/T]ACTGCCGGCCTCGTT | 10055 |
| rs546027679 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47137309 | AGGAGAATTGTTTGA[A/C]TCCAGGAGGCAGAGG | 10055 |
| rs546030464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47156934 | CCAGAATTGGTTTCA[C/T]TGAACTGAGAGGAAA | 10055 |
| rs546094680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47206103 | CCATTGTTGGTGGTA[A/G]TTTCTCACATCCCCA | 10055 |
| rs546240445 | in-del | -/T | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129743 | TGGGGCCATCCCTGG[-/T]TTTTTTTTTTTTTTC | 10055 |
| rs546291846 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47192187 | GCACTCATGTGATCT[A/T]CACGATAACCTGGTG | 10055 |
| rs546295428 | in-del | -/TT | 0.00478085 | 0.0486577 | intron-variant | SAE1 | GRCh38.p7 | 19:47169247 | CCAGAGGTTTTTTAG[-/TT]TTGTTTTGGTTTTTT | 10055 |
| rs546312505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47192354 | CTCCTGGGTTTGAGC[A/G]ACTCCTGCCTCAGGC | 10055 |
| rs546336188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47137675 | CTAATTTTGTGTGTG[C/T]ATGGCGTATGCCGTA | 10055 |
| rs546414475 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47207849 | CCATGTTGCCCAGGC[A/T]GGTCTCGAACTCCTG | 10055 |
| rs546557290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47131454 | ACAGGGGAGACTGGA[C/T]TGGCCAACCGGACAG | 10055 |
| rs546587554 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47178560 | CTCATTGCAACCTCC[A/G]CCTTTTGGATTCGTG | 10055 |
| rs546594347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47138187 | TAGCTGGGATTACAG[G/T]CGCCTGCTACCGCGC | 10055 |
| rs546608914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47145414 | GGCCTCCCAAAGTGC[A/G]GTGATTACAGGTGTG | 10055 |
| rs546624276 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47132247 | GGATTACAGACGTGA[G/T]CCACTGTGCCCAGCT | 10055 |
| rs546672935 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47144555 | ACACAAAAAATTAGC[A/G]GGGCTTGGTGGCGGG | 10055 |
| rs546697691 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47196226 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 10055 |
| rs546737100 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47159501 | TGTTCAGTGTACTGG[G/T]GGCTGTTAACTGCAG | 10055 |
| rs546744929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47208668 | AACCTCAGGTGATCC[A/G]CCCACTTCAGCCTCC | 10055 |
| rs546770768 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47158700 | GCAGAATGCCTACTG[G/T]GTGCAAGGCACTGTG | 10055 |
| rs546801713 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47208243 | GTCATTGTTTTAGTT[G/T]TAAGGTGTTTTTTTG | 10055 |
| rs546857201 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47192053 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAGA | 10055 |
| rs546861478 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47133500 | AAAGTGCTGTGATTA[A/C]AGGCGTGAGCCACTG | 10055 |
| rs546887113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47165237 | TGGGATTACAGGCAC[A/G]TGCCACCATGTCCGG | 10055 |
| rs546933271 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SAE1 | GRCh38.p7 | 19:47140082 | AGCTGAGATTACAGG[C/T]GCCTGCCACCACTCC | 10055 |
| rs546974953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47194061 | AACCCATTTCTGAAC[A/G]TCTCCCAGGCTTCAG | 10055 |
| rs547021544 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47168090 | CCCAGCTACTGGGGG[C/T]GCTGAGGCACGAGAA | 10055 |
| rs547029444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47152344 | CACTTGGTCTGTAAC[C/T]TTTTCTTTTGTCCTT | 10055 |
| rs547072051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47160743 | ACCATGTTGACCAGG[A/G]TGGTCTCAATCTCCT | 10055 |
| rs547081315 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47200337 | TCCTGGGCTCAGGCA[A/G]CACTCTCATCTCGGC | 10055 |
| rs547149012 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47188836 | AGAGAGAAGGTACAG[A/T]GGACGGGACAGGCAA | 10055 |
| rs547191201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47132789 | GCTTGTCAGGAGACT[A/G]AGGTGGGAGCATCAC | 10055 |
| rs547217694 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SAE1 | GRCh38.p7 | 19:47202863 | TGCAGTAAGCCAAGA[C/T]CGCGCCACTGCACTC | 10055 |
| rs547278097 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47167439 | TAGAGACGGAGTTTC[A/G]CCATGTTAGCCAGGA | 10055 |
| rs547285091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47195502 | ATCCATTTATGGGGA[C/T]TGAGATAGTTTTCAT | 10055 |
| rs547334539 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47154655 | GCCCACCACCACGCC[C/T]GGCTAGTTTTTTGTA | 10055 |
| rs547342758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47203025 | AGCACACAGCATTGT[A/G]TTCAGGAGTAGGAGC | 10055 |
| rs547390868 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47142731 | GCTGTTTTCTCTATC[G/T]GGAATGTTCTGCTGC | 10055 |
| rs547399786 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47202510 | CCAGGATGATCTCGA[C/T]CTCTTGACTTTGTGA | 10055 |
| rs547400242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47160371 | GAACTACAGGTGCGC[A/G]CCACCACGCCCAGCT | 10055 |
| rs547480031 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47135125 | GGTAATAATCACATC[A/G]GGGTAAATGGGGTAT | 10055 |
| rs547517695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47175004 | GTGAGGCACCGTGCC[C/T]GGCAGTGAGAACATT | 10055 |
| rs547554573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47182224 | TAGTTCTCTTCAGAA[A/G]AAACTTCTTATTTTA | 10055 |
| rs547579945 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47140342 | CGGTCTTCTGACCTC[A/G]TGATCTGCCTGTCTC | 10055 |
| rs547595005 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47141431 | ACAGGCATGAGTCAC[C/T]GGGCCCGGCTGAATA | 10055 |
| rs547596296 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47144227 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCACA | 10055 |
| rs547632563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47147924 | CCACCACGCCTGGCT[A/G]ATTTTTTTGTATTTT | 10055 |
| rs547643942 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47135762 | TGCTGGGATTAGAGG[C/T]GTGAACAGCAATGCC | 10055 |
| rs547717790 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47178757 | GTTTATAGGCATGAG[C/G]CATCGTGCATAGCCT | 10055 |
| rs547798618 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47143036 | GAATGAATTGTTTTG[G/T]GCAGTATGGATTAGA | 10055 |
| rs547801453 | snp | C/T | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47176247 | TTGGATGTACCGTCA[C/T]CTATGACCAGTCTCA | 10055 |
| rs547837480 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47158418 | TTTGAGACGGATTTC[A/G]TCACAATCAGGTCTC | 10055 |
| rs547888568 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47181303 | CTTGGGCAACAAGAG[C/T]GAAACTCTATCTCAA | 10055 |
| rs547935189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47149500 | TTTAAACCACTGGAA[A/G]ACAGAGATTTAATCC | 10055 |
| rs547985227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47137376 | CTGGGTGACAAGAGC[A/G]AAACTCTGTCTCAAA | 10055 |
| rs547993373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47164414 | CCTCGTGATCCGCCC[A/G]CCTTGGCCTCCCAAA | 10055 |
| rs548002961 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47135119 | ACAATGGGTAATAAT[C/G]ACATCAGGGTAAATG | 10055 |
| rs548027832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47170247 | AGACAGAGTCTTGCT[C/T]TGTCACCCAGACTGG | 10055 |
| rs548042290 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47162743 | TGCCTGTAATCCCAG[A/C]ACTTTGGGAAGCCAA | 10055 |
| rs548086457 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130200 | ATTTTTATTATTATT[C/G]TATGTCCAGGGCTGG | 10055 |
| rs548120181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47136557 | CTGGAGTATGGTGGC[A/G]TGATCTCAGCTCACC | 10055 |
| rs548121236 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47168809 | GGGTTTCACTATGTT[G/T]GTCAGGCTGGTCTTG | 10055 |
| rs548172520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176554 | AGTAGTGTGCCCACT[A/G]GAGTCCCCACAGGGT | 10055 |
| rs548189786 | snp | C/G | 1.65946e-05 | 0.00288046 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150217 | GTAACTCCAGAAGAT[C/G]CCGGAGCTCAGTTCT | 10055 |
| rs548207745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47184098 | AGAGTCAAGCTCTGG[A/G]ATCGCCTGACATTTT | 10055 |
| rs548213206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47165111 | TTTTTTGAGACGGAG[C/T]CTTGCTCTCTTGCCC | 10055 |
| rs548235219 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47205443 | TGGAGGGGGAAGAAA[A/C]GTGTGCAATGGCCAT | 10055 |
| rs548251306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47164410 | CTGACCTCGTGATCC[A/G]CCCGCCTTGGCCTCC | 10055 |
| rs548304908 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47132431 | TAATTTTTGTTTTTT[G/T]TTTTTTTTGTAGGAT | 10055 |
| rs548330566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47157390 | AAAAGCTGCTTTGTG[A/G]GTGCTGTCAGTTTAT | 10055 |
| rs548334962 | snp | A/C/G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47130854 | CGGGCGTGCTGCCGG[A/C/G/T]GGCGGTAGGTGGCGC | 10055 |
| rs548410069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47177104 | TCTTAACTTGCTCAG[C/T]CTCTGTTCTGATGAG | 10055 |
| rs548466090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47192423 | CCAGCTAATTTTTGT[A/G]TTTTTAATAGAGATG | 10055 |
| rs548479630 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47145227 | AGCTGGTCTTGAACT[C/G]CGACCTCAGGTGATC | 10055 |
| rs548596622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47207189 | GAGGTTGCAGTAAGC[C/T]GAGAATGTGCCTCCC | 10055 |
| rs548601170 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47172083 | ACCAGCACACCCAGC[C/T]AATTTTTGTATTTTT | 10055 |
| rs548687957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47186540 | TGAGGGTGCAGGTCC[C/T]TCAGCCTTCTTGCTT | 10055 |
| rs548759845 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47171300 | TAATTTTTATTTTAA[-/T]TTTTTTTTTTGGAGA | 10055 |
| rs548778133 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47138274 | GTCTTGAACTCCTGA[C/T]CTCAGGTGATCTACC | 10055 |
| rs548822543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47178133 | GTAGTCCCAGCTACT[C/T]GGGAGGGGGAGGCAG | 10055 |
| rs548824250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47151842 | CTGAAGTGTGAGGCC[A/G]GTTGATTGTGTAATG | 10055 |
| rs548901422 | in-del | -/GAG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137187 | TGAGGTCAGGAGTTC[-/GAG]ACTAGCCTGGCCAAC | 10055 |
| rs548973531 | in-del | -/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47152381 | AGATAAAGTTTCACA[-/C]CGCAATCTGTGGAAA | 10055 |
| rs548998797 | snp | A/G | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47185054 | CGAACTCCTGACCTC[A/G]GGTGATCCACCCGCC | 10055 |
| rs549000979 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47187015 | CTAGCATAGGGTAGG[G/T]GTGGAGGGGGGGTGC | 10055 |
| rs549045146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47178673 | AGACAGGGTTTCGCC[A/G]TGTTGGCCAGGCTGG | 10055 |
| rs549132665 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47146855 | TGGACTCCGGAGACA[C/G]CACACAGAAGCAGGC | 10055 |
| rs549169358 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47153686 | GTCTCCAAGTTTCTT[A/G]CCTGTAAAATCAAGA | 10055 |
| rs549192778 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47201441 | CAGTGGCGTGATCTC[A/G]GCTTATTGCAACCTC | 10055 |
| rs549202202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47194674 | GGGAACAAGAATGCC[C/T]GCCCGCCCGCAGGCA | 10055 |
| rs549233935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47159614 | GGCTGAAGTGCAGTG[A/G]TTCAAACACTGCTCA | 10055 |
| rs549272613 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47166877 | GTGAAAACATCTTGT[A/G]TACTATCTTTAACAA | 10055 |
| rs549272743 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47158775 | GCTGATAAAGAAGCT[A/G]TGAGAAATTAAGTGA | 10055 |
| rs549330093 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167171 | GTTGGCCAGGCTGGT[C/G]TCCAATTCCTGACCT | 10055 |
| rs549354428 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47187973 | TAGAGTAGTGACATC[A/G]CCTTTGCCCCACAGA | 10055 |
| rs549365259 | snp | C/G | 1.64993e-05 | 0.00287218 | intron-variant | SAE1 | GRCh38.p7 | 19:47155096 | AAAATTACATTCTCT[C/G]CCCTTGTCACCCTCT | 10055 |
| rs549419269 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47146145 | GCTAAAAGTAGTTTG[G/T]TGTTTTTAGAGTGTG | 10055 |
| rs549490420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47187255 | GCCCAGCTATGTCAC[C/T]CCTCTGAGCTTCACA | 10055 |
| rs549520089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190631 | CGAGGTATGTGGATG[A/G]TGCCAGCCTGCCGGC | 10055 |
| rs549545153 | snp | A/G | 3.2981e-05 | 0.00406071 | intron-variant | SAE1 | GRCh38.p7 | 19:47203788 | ACCATGACTTTGTAT[A/G]TGTGCTGACAGAGAG | 10055 |
| rs549593263 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47167540 | CCACTGCGCCCAGCC[A/T]ACAATTTGAACTTTT | 10055 |
| rs549612881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47168124 | CTTGAACCCAGGACA[C/T]GGAGGTTGCAGCGAG | 10055 |
| rs549631901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47173456 | TTGCTCCTAGATATC[A/G]GTTTTGTCCCCTCAG | 10055 |
| rs549713560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47180547 | TATCAGATGCTTTTA[C/T]GCTATGCCTGGTGGC | 10055 |
| rs549722851 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47142266 | GTAGGCGCCTGTAAT[A/C]CCAGCTACTCGGGAG | 10055 |
| rs549738329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47147964 | ATGGGGTTTCACCGT[A/G]TTAGCCAGGATGGTC | 10055 |
| rs549746766 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SAE1 | GRCh38.p7 | 19:47203176 | GGCCCAGAAGGGCTG[C/G]TTTCTATGTGGGTTG | 10055 |
| rs549778805 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47196497 | GTCTCCCAAGTAGCT[G/T]GGACTACAGGCACGT | 10055 |
| rs549863334 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210630 | ATCAGTCTCTTTCCT[A/G]TTCTGATCCTGCAGC | 10055 |
| rs549882821 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47143191 | GCTCACTGCAACCTC[C/T]GCCTCATGGTTTCAA | 10055 |
| rs549914431 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47195517 | TTGAGATAGTTTTCA[A/T]AGTAAAGGAAGTTTT | 10055 |
| rs549924196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47142946 | CATGAGGGCAGGGAC[C/T]ATGTCTGATTCACCG | 10055 |
| rs549950311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47169612 | GTCTTCCTTCAGTGC[A/G]GGGAGTTTGTGTTGT | 10055 |
| rs549960118 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47205589 | CTGAGGCTCCCTGTA[A/G]ACAAACTGCAGGAAA | 10055 |
| rs549989809 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47198998 | GAGGCTGAGGCTAGA[A/G]CATCGCTTGAGCCCA | 10055 |
| rs550013478 | in-del | -/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47171749 | GATTACAGACGTGAG[-/C]CACTGCACCTGGCTG | 10055 |
| rs550023146 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47204870 | CCCCATGAACACACC[A/G]GGAGCCCCTCAAGGC | 10055 |
| rs550086368 | in-del | -/AGTC | | | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210650 | GATCCTGCAGCAGTT[-/AGTC]GGGGAGAAAAGTGGT | 10055 |
| rs550095991 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47174998 | ACAGGCGTGAGGCAC[C/T]GTGCCCGGCAGTGAG | 10055 |
| rs550143031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47197734 | CCACAGCTCCTTAGT[A/G]TTCTAGAGTGTGAAG | 10055 |
| rs550147791 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47137524 | TTTTTTTTCTCGCTC[G/T]GTTACCCAGGCTGGA | 10055 |
| rs550195565 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SAE1 | GRCh38.p7 | 19:47188533 | GTTACCACAGCAAGT[A/G]TATCGGCTTTTCTAG | 10055 |
| rs550201842 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129405 | GTTCAAGCGATTCTC[C/T]GGCCTCAGCCTCCCA | 10055 |
| rs550213631 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47139471 | GATTACAGGTGTGAC[C/T]CACTGCGTCCAGCCT | 10055 |
| rs550266859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47175070 | TTAAGATCAAAGTTA[A/G]CACATTAGAAGTGGA | 10055 |
| rs550336124 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47135849 | CCTAGGCTGGAGTAG[C/G]CTGGAGTGCAGTGGC | 10055 |
| rs550362435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47131421 | TTCGAGGGTATGGGA[C/T]CTGGTTCCGTGCTGC | 10055 |
| rs550425906 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47156471 | CGACAGAACGAGACT[C/G]TGTCTCCAAAAAAAA | 10055 |
| rs550453846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47170061 | CTCAGTGATCACTTG[A/G]GAAAGGGGTGGTCAC | 10055 |
| rs550460155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47155975 | TTATCTCTTGACCTC[A/G]TGGTCCACCTGCCTC | 10055 |
| rs550506349 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47192281 | TTTGAGACAGAGTCT[C/T]GCTCTGTCACCCAGG | 10055 |
| rs550510017 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, missense, intron-variant | SAE1 | GRCh38.p7 | 19:47130869 | CGGCGGTAGGTGGCG[C/G]GCGGGTCCGGCGGGC | 10055 |
| rs550529763 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SAE1 | GRCh38.p7 | 19:47164207 | GAAGTCTCGATCTGT[C/T]GCCCAGGCTGGAGTG | 10055 |
| rs550545285 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47164418 | GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 10055 |
| rs550552651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47152254 | TTACTGGAATACAAC[C/T]TGGAGGCCCCAGAGC | 10055 |
| rs550562835 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47143952 | AACTGAAAATGCAGA[C/G]TGGCCTGGAGGCTTC | 10055 |
| rs550576015 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47171246 | CCAAAGTGCTGTGAT[A/T]ACAGGTGTGAGCCAC | 10055 |
| rs550587753 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47151876 | GTGCATGGGGCCATG[C/T]TGACCGCCTTGCAGG | 10055 |
| rs550624414 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47158032 | CTTGATTCAGATGCT[C/G]CCCTTTTGCCTAATT | 10055 |
| rs550641651 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47191827 | TTGGGAGGCCAAGGC[A/G]GGCCGATCACAAGGT | 10055 |
| rs550646588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47150880 | TTGACCATGTTGCCA[C/T]GGATAACTAGAGAAA | 10055 |
| rs550693328 | in-del | -/AT | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47173345 | CCTGCCACAGAAGTC[-/AT]ATAGCTACTGTTTCT | 10055 |
| rs550702173 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47168894 | CAGGCGTGAGCCACT[C/G]TGCCTGGACTTGTAA | 10055 |
| rs550741343 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47189138 | CCCAGGGCTTTGCCT[C/T]AGGAAACAGGCTGTT | 10055 |
| rs550848546 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47186853 | GCGGCCACTCCAGAG[G/T]TGAAGTTTTCTAGAG | 10055 |
| rs550881445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47139968 | TTTGAGACGGAGTCT[C/T]GCTCTTTCGTCCAGG | 10055 |
| rs550988098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47209083 | ACCACTGCCCTAGAC[C/T]GCTTTTAGAATTTTT | 10055 |
| rs550993099 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47199621 | ATCACTTTGAATGCC[A/C]AAGTAGTCACTTGGC | 10055 |
| rs550993100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47208167 | CTGCCACCTTTCTCA[A/G]TTGAATAGTCATGAA | 10055 |
| rs550997079 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47203391 | GACAGATATAGGAAG[C/T]ACAGATATAGTCTTT | 10055 |
| rs551031457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47200146 | CGCTGTGTTAGCCAG[A/G]ATGGTCTTGATCTCC | 10055 |
| rs551054446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47165183 | CAACCTCAGCCTCCT[A/G]GGTTCAAGCGATTCT | 10055 |
| rs551056144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47207399 | TAGCCCCACCTTCCT[C/T]ATGAATGATGGGACG | 10055 |
| rs551076150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47172483 | TTTGCCAAGGTTTGG[A/G]TTTGACTTGAGCATC | 10055 |
| rs551177852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47139109 | GGCACGTGCCACCAC[A/G]CCTGGCTAATTTTTG | 10055 |
| rs551225864 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209831 | ACCCTGACAAACAAC[A/T]GGTGGCATCTGGTGT | 10055 |
| rs551243904 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47186616 | TCTTGTTTTTGAGCT[C/T]GTTTCTGAGAAAGTG | 10055 |
| rs551262733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47202434 | CTGGGACTACAGGCT[C/T]ACCCCACCACACCAA | 10055 |
| rs551290075 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47170032 | CCTTGGGTGGCATTC[G/T]TCATTGGCTAGTTCT | 10055 |
| rs551353862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47160335 | TAAGCGATTCTCCTG[C/T]GTTAGCCTTCCGAGT | 10055 |
| rs551360227 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182052 | CTGCCTCCCAAAGCA[C/T]TGGGATAACAGACGT | 10055 |
| rs551392391 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47167502 | GCCTTGGCCTCCCAA[A/T]GTGCTGGGATTACAG | 10055 |
| rs551506937 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47141369 | CTGGTCTCGAACTCC[G/T]GACCTCAGGTGATCC | 10055 |
| rs551515703 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47194703 | CAGGTTACCTGTGGA[C/T]AAGGTGTAGTGGGCA | 10055 |
| rs551593292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47147072 | AATTCTGAGATGGAA[A/G]CTTGGGGACAGCCAC | 10055 |
| rs551610032 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47195117 | TGGAGTTCAGTGGCA[C/T]GATCTCGGCTCACTG | 10055 |
| rs551617999 | snp | C/T | 0.00155236 | 0.0278167 | intron-variant | SAE1 | GRCh38.p7 | 19:47197230 | TCTTTTTCTTATTCC[C/T]AGTGCTCTTAAAGTT | 10055 |
| rs551626996 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47144650 | CTTGCAACGAGCCGA[G/T]ATCATGCCACTGCAC | 10055 |
| rs551660474 | snp | A/G | | | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150239 | CTCAGTTCTTGATTC[A/G]TACTGGGTCTGTTGG | 10055 |
| rs551730046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47168691 | CACTGCAACCTCCCC[C/T]CTCCTAGGTTCAAGC | 10055 |
| rs551756591 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184720 | CCGGCCTCGTTCTGT[C/T]GTATTTTTTTACGTA | 10055 |
| rs551784337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47155737 | GTGAGCCACCATGCC[C/T]GGCCCCATACCCTTT | 10055 |
| rs551811518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47140874 | ATTTAATTTTTTTTG[A/G]GACGGAGTCTGTCAC | 10055 |
| rs551851580 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47147853 | AAGCTCTGCCTCCCG[A/G]GTTCACACCATTCTC | 10055 |
| rs551875366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47188141 | ACAACTTGAGCTCAG[A/G]AGTTTGAGACCAGCC | 10055 |
| rs551890787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47180731 | AGGAGGATGAGATGG[A/G]AGGATCGGTTGAGCG | 10055 |
| rs551940835 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210693 | AGAAGGGCCTCTGTT[C/G]CTCAACCCTGCATCA | 10055 |
| rs551989441 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47161751 | GTTACCACCCTCCTC[A/C]GTTGGGTTTCTCATT | 10055 |
| rs552085835 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47164895 | CTGACCTCGTGATCC[A/G]CCTGCCTCAGCCTCC | 10055 |
| rs552098721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47135081 | ACATTTTGGGGGTAT[A/G]TGAGATACTTTGATA | 10055 |
| rs552109666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47135911 | CAGGTTCACGCCATT[C/T]TCCTGCCTCAGCCTC | 10055 |
| rs552111059 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47189922 | GTTATAGCGCTAACC[A/T]GATGTTATGAACTGA | 10055 |
| rs552145756 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47142317 | TGGACCTGGGAGGCG[A/G]AGGTTGTAGTGAGCT | 10055 |
| rs552175221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47183043 | GCCTCTGCCTCCCGA[A/G]TAGCTGGGATTACAG | 10055 |
| rs552182068 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47205722 | CCACTGTCTGCCACA[C/T]AAAGACAGTGTTTTT | 10055 |
| rs552189998 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47141249 | TCAAGTGATCTGCCC[A/G]CCTTGGCCTCCCAAA | 10055 |
| rs552192406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47171077 | CCTCCTGGGTTCAAG[C/T]GATTCTTCTGCCTCA | 10055 |
| rs552212033 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190828 | TCCACTTCTCACCCA[C/T]TGAACTTACAGCTTG | 10055 |
| rs552258223 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47206439 | ATGGAAAGCTTACAC[C/T]AGGAGATGGGTCAAG | 10055 |
| rs552263786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176497 | TATTTTTTGCATGAG[C/T]GGTTTTTGCTTGTCT | 10055 |
| rs552312756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47191910 | AATACAAAAATTAGC[C/T]GGGCGTGGTGATGGC | 10055 |
| rs552332377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47136400 | TCCTTGGCCCCCCAA[A/G]GTGTTGCAATTACAG | 10055 |
| rs552382783 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129451 | AGGCGTGTGCCACCA[C/T]GCCCGGCTAATTTTT | 10055 |
| rs552419005 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47197919 | AATTTATCATTTGGT[A/C]AGCATTGCCACCTTG | 10055 |
| rs552433949 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191428 | CATCAAATGTTAAAC[A/G]CTAGTCCTGTCAGTC | 10055 |
| rs552608500 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47174794 | TAGCCAGGATGGTCT[C/T]GATGTTCTGACCTCG | 10055 |
| rs552710991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47206136 | CTCACACAGCCCCCT[C/T]CTTCCTGCCTGCTGG | 10055 |
| rs552743286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47208745 | TAGTTTTCATATAGA[C/T]GGGATCTCACCATGT | 10055 |
| rs552744388 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47151912 | TTTGGCTGGTCCTTG[C/T]AGGTTTTATAGTTAC | 10055 |
| rs552744651 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47144331 | AGAGTGAGACTTTGC[C/T]TTAAAAAGAAATAAA | 10055 |
| rs552750152 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130038 | GCCAGGCTGGTCTCC[A/G]ACTCCTGATTTAAAG | 10055 |
| rs552797252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47144014 | TCATTTAGGTCTGAG[A/G]CGAGCTCAGGAGTAT | 10055 |
| rs552814616 | in-del | -/TTTTAGTA | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47171629 | GCTAATTTTTTGTAT[-/TTTTAGTA]TTTTTGTATTTTTTT | 10055 |
| rs552930905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47139161 | TTCACCATATTGGCC[A/G]GGCTGGTCTCGAACT | 10055 |
| rs552941196 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47157310 | TTGAGGCCCAGTCAA[G/T]ATTTATCTGAATAGC | 10055 |
| rs552951662 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | SAE1 | GRCh38.p7 | 19:47171644 | TTTAGTATTTTTGTA[-/T]TTTTTTTTGTATTTT | 10055 |
| rs552953699 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47161792 | TCTTCTTACTACTTA[C/T]GTATGTATTTCCAAG | 10055 |
| rs552999223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47157065 | GATTCTAAAGAGTGC[A/G]GAAACCACAAAAGAG | 10055 |
| rs553008509 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47144896 | GAGTGCAATGGCGCA[A/G]TCTCCGCACACTGCA | 10055 |
| rs553050232 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47186650 | GCTCCTTTTCCCCAT[A/C]AACAACTTTCATCCG | 10055 |
| rs553052778 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47171316 | TTTTTTTTTTGGAGA[C/T]GGAGTCTAGCTCTGT | 10055 |
| rs553091532 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47170490 | CAACCAACTTCTCTT[C/T]ACCGCCCCCCGCCTT | 10055 |
| rs553128217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176702 | GCTGTCCGCATGCAT[A/G]TGCTTGCCATGTTTA | 10055 |
| rs553138332 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47152610 | TATGAAATGTGTATA[C/T]GTTCGTGGATTACAG | 10055 |
| rs553146297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47138065 | TTTATTTTTTTGAGA[C/T]GGAATTTCTCTCTTG | 10055 |
| rs553173369 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47192205 | CGATAACCTGGTGAG[C/T]GGGTAATTATTATCA | 10055 |
| rs553197679 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47198902 | GGCCAACCTTGACAA[C/G]ATGGTGAAACCCTGT | 10055 |
| rs553222022 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47185539 | CTGAACTCCTGACCT[C/T]AAGTAATCCTCCCAC | 10055 |
| rs553232811 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47199696 | CTGCCGCTTGCCACT[A/G]GCTGACTGGCTGGGA | 10055 |
| rs553233457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47172765 | TTGAAAAGTGTACAC[A/G]CCAAAAAAAAAAAAG | 10055 |
| rs553235236 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47169566 | GAGTTAAAGGGCCAG[A/G]GTGGAAGCAGGTCTT | 10055 |
| rs553239457 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47164516 | TCCTCTTCTTGCCTA[G/T]CCATAATCTATTTTA | 10055 |
| rs553270607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47172114 | AGTAGAAACGGGGTT[C/T]CACCATGTTGGCCAG | 10055 |
| rs553288307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47178270 | GAAATCTATCTATCT[A/G]TCAGTCAGAATCACT | 10055 |
| rs553309043 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47173277 | GCTGGGATTAGAGGC[A/G]TGAGCCACCGCGCCC | 10055 |
| rs553312696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47131993 | GGAGTGAGCCACCGC[A/G]CCAGGACGTCTTTTG | 10055 |
| rs553372650 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47133682 | ATATATTCTGGATAT[A/G]TTTTGAAGGTAGAAG | 10055 |
| rs553374397 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47176024 | CCATTTTTTTGTCTT[C/G]TAAATTTCTAGGAGA | 10055 |
| rs553396651 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47168313 | ATATTTCAGTCTGTA[-/T]TTTTTTCTCTCTCTC | 10055 |
| rs553410368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47178868 | CCCAAGTAGCTGTTC[A/G]ATATAGTATTTTGAC | 10055 |
| rs553429259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47186176 | ACCCAGGAGGCACAG[C/T]TTGCGGTGAGCCGAG | 10055 |
| rs553432824 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47132489 | TCTTGAACTCCCAAG[C/G]TCAAGCGATCCTCGG | 10055 |
| rs553437503 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47208166 | ACTGCCACCTTTCTC[A/G]GTTGAATAGTCATGA | 10055 |
| rs553447408 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210957 | CTTCAAACTTTTCCA[C/T]CCTGTACCTCTAACG | 10055 |
| rs553481917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47201702 | GCAGTGGCACCATCT[C/T]GGCTCACTGCAACCT | 10055 |
| rs553498070 | snp | C/G/T | 0.00676944 | 0.0578265 | intron-variant | SAE1 | GRCh38.p7 | 19:47142967 | TGATTCACCGCCTTA[C/G/T]TTCCACACCATAGAA | 10055 |
| rs553520699 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47153103 | TACTTTTTTTTTTTA[A/T]ATTATGTATTTATTT | 10055 |
| rs553541465 | snp | A/G | 1.64792e-05 | 0.00287042 | synonymous-codon, utr-variant-3-prime, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209172 | AGGCCCTGTCTCAGC[A/G]GGACCCTCCTCACAA | 10055 |
| rs553551816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47208498 | CAGGCTGGAGTGCGG[C/T]GGCGCAATCTCAGTT | 10055 |
| rs553664626 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47134020 | GGCGCCCGCCACCAT[A/G]CCCAGCTAATTTTTG | 10055 |
| rs553681994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47194811 | CAAAGTGCAGTGGCG[C/T]GATCTCAGCTCACTG | 10055 |
| rs553799436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47146686 | AGAAAAGTACTGGCC[C/T]ATCCAAGGCCCCAGT | 10055 |
| rs553803024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47152526 | TTTGCTTGTCCCTGT[A/G]GCTTATTTGGATTTT | 10055 |
| rs553809020 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SAE1 | GRCh38.p7 | 19:47174382 | AGGTCAGTAATAATC[A/C]TACAATGTTTTATTT | 10055 |
| rs553843488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47159081 | GGTTACTCTGTAATA[A/G]CTCTTTAAAAATTAA | 10055 |
| rs553897622 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210890 | CTTGGTCACAAGGGG[A/G]AGCAGGTGGGTCTGG | 10055 |
| rs553909585 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184313 | GTGACTTTTAAATCC[A/G]TCGTGACCATAAGCC | 10055 |
| rs553995052 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47173680 | TCCCCACCCAGCTCT[A/C]ACATCAAAAAATGTT | 10055 |
| rs554066523 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47147254 | ACTGTTACCCTTGCC[A/G]GAATGCAGTGGGCAT | 10055 |
| rs554075792 | in-del | -/AAATA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137399 | GTCTCAAAAATAAAT[-/AAATA]AAATAAAATAAAGTA | 10055 |
| rs554121030 | snp | A/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47210034 | TTTTAACAGAACCCC[A/G/T]GTCACATGCGGCTCA | 10055 |
| rs554142682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47154916 | TGCTCTGTTTTTCCC[A/G]CAATAATTTCCTGAG | 10055 |
| rs554157639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47135489 | CAGTGCCCTCCCTGT[C/T]GTTGTAAATGACAGG | 10055 |
| rs554165710 | in-del | -/T | 0.392511 | 0.205404 | intron-variant | SAE1 | GRCh38.p7 | 19:47131698 | TAGCTTAGGGAATTC[-/T]TTTTTTTTTTTTTTT | 10055 |
| rs554196421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47142410 | AAAAAAAGGTAAAAG[C/T]AATTCCTGTGTACAT | 10055 |
| rs554222224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47175247 | TTGTTTCCATGTTCC[C/T]GGCACCTAAGTTGAT | 10055 |
| rs554256430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47160586 | ATTTCTAGTAGAGAT[A/G]GGGTTTCACCGTGTT | 10055 |
| rs554293528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47167830 | AATAATTTTTTTTAG[A/G]GACGGGATCTAACAG | 10055 |
| rs554341719 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47148874 | CTGCCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC | 10055 |
| rs554344104 | in-del | -/C | 0.00358779 | 0.0422022 | intron-variant | SAE1 | GRCh38.p7 | 19:47152309 | TCACCAGTTCATTGT[-/C]CTAAGCCTGAATGGA | 10055 |
| rs554361176 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | SAE1 | GRCh38.p7 | 19:47182494 | GTGTGTGTGTGTGTG[C/T]GTGCGCGCACGCACG | 10055 |
| rs554380633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47155406 | GCCCAGTGATTCCAG[A/G]TGGGATTTTTCAAGA | 10055 |
| rs554411964 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SAE1 | GRCh38.p7 | 19:47195981 | TCAAGCGATCCTCAC[A/G]CCTTGGCCCCCCAAA | 10055 |
| rs554458160 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47169320 | ACGCGATCTTGGCTC[G/T]CTGCAAACTCCACCT | 10055 |
| rs554518067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47161235 | AGGCTGATCTCAAAC[C/T]CCTGGCCTCAAGTGA | 10055 |
| rs554735528 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190157 | TCAGCATCCTGAGTT[A/C]ATTAAAAGGTGCAGA | 10055 |
| rs554739152 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47149965 | TTGTAGTCCCAGCTA[C/T]TTGGGAGGCTGAGGC | 10055 |
| rs554775805 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47156153 | GGTGAGCACCTGTAG[G/T]CCCAGCTACTCATAG | 10055 |
| rs554872949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47191971 | AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCG | 10055 |
| rs554877818 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130641 | GCAGAATTTAAGTGC[C/T]ACATAAGTGACCACG | 10055 |
| rs554891673 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129512 | CTTGGCCGGGCTGGT[C/T]TCGAACTCCTGACTT | 10055 |
| rs554984856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47150596 | CTGTAGTTGTTGGTG[A/G]CTTGCTGTCTGCTGG | 10055 |
| rs555001634 | snp | G/T | 1.64868e-05 | 0.00287109 | intron-variant | SAE1 | GRCh38.p7 | 19:47143608 | GGATCACGAACAGGT[G/T]CGCTGTTGTGAGCTC | 10055 |
| rs555019150 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47156771 | TTGTTAATGTAGTTT[A/G]TATTAGGGGCTCAGC | 10055 |
| rs555066120 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47145313 | GCCATGCCTGGCTAA[C/G]TTTTGTTATTTTTAG | 10055 |
| rs555136540 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47169589 | CAGGTCTTTGGAAGC[G/T]TGGCTCTGTCTTCCT | 10055 |
| rs555142967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47138563 | ACAGGTTTGTTTTGG[C/T]GTGTCTATTAATTCA | 10055 |
| rs555222405 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47166571 | CTCCACCCCCAACTC[C/T]GTTTCATCATATAGT | 10055 |
| rs555226554 | in-del | -/AA | 0.0138799 | 0.0821421 | intron-variant | SAE1 | GRCh38.p7 | 19:47166633 | AGTCAGGCAAACAAC[-/AA]AGACTCCGAATTGAG | 10055 |
| rs555237767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47193286 | GGCTGGTCTTGAACT[C/T]CTGACCTCAGGTGAT | 10055 |
| rs555243415 | snp | A/G | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176711 | ATGCATGTGCTTGCC[A/G]TGTTTAGATATTGGG | 10055 |
| rs555253048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47137003 | AGGCTGATAAAATGT[A/G]CAAATTGTGGGGCAT | 10055 |
| rs555268560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47200373 | GCGTAGCTGGGACTA[C/T]AGGCGTGTACTACCA | 10055 |
| rs555303041 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47186251 | CTCAAAAATAAAAAT[-/A]AAAAAAAAAATAATA | 10055 |
| rs555308874 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47152423 | CAGGACTTGTTTATC[G/T]TCTTTATCTTAACAT | 10055 |
| rs555317355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47132957 | ATGGTGAAGTGAGAG[A/G]GTTGTTTTGATAGGT | 10055 |
| rs555364945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47207662 | CCCACCCCTCTCTCT[C/T]GCTCTCTGTTGCCCA | 10055 |
| rs555392863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47139194 | TGACCTCAAGTGATC[C/T]GACCGCCTCGGCTAA | 10055 |
| rs555441369 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47165280 | TTTTTAGTGGAGACG[C/G]GGTTTCACCATGTTG | 10055 |
| rs555442968 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47157807 | TTCCAACCCCAAGCC[C/G]TTAAGGTTACGAGGC | 10055 |
| rs555479735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47164884 | GTCTCGATCTCCTGA[C/T]CTCGTGATCCGCCTG | 10055 |
| rs555562618 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47144928 | CCTCCGCTTCCCGGG[C/G]TCAAGTGATTCTCCT | 10055 |
| rs555565390 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SAE1 | GRCh38.p7 | 19:47186287 | TCATTGGAGCATTTT[A/G]GATTTGGGATTCTTA | 10055 |
| rs555578221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47159937 | GGCCTCAAGTGATCC[A/G]CCCACTTTGGCCTCC | 10055 |
| rs555597233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47199869 | ACAGTGTCATCAGCC[A/G]CTGACCTCACGGTGC | 10055 |
| rs555599668 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47151964 | TTTGATCAATTGGTT[G/T]CATGTTCACCTGTGG | 10055 |
| rs555604045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47192611 | GCAGCGGTGTGATTT[C/T]GGCTCACCGCAACCT | 10055 |
| rs555624666 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47179434 | ATTGCTTGAACCCTG[C/G]AGGCAGAGGTTGCAG | 10055 |
| rs555701679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47158352 | GAAAATGCCTAGCCC[A/G]GAAATAGGTGCTCAG | 10055 |
| rs555752128 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47205215 | ATGTCAAGTTTGAGC[G/T]TGGGAGGACAGTTTG | 10055 |
| rs555754805 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47179764 | GAGACGGGGTTTCAC[G/T]GTGTTGCCCAGGGTA | 10055 |
| rs555755576 | in-del | -/TG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47153618 | TTCCTACCAAGAGAC[-/TG]TGAGAACTCTTCTCT | 10055 |
| rs555761786 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47167200 | CTCTAGTGATCCACC[C/T]GCCTTGGCCTCCCAA | 10055 |
| rs555764604 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47204357 | CGCCTGCCACCACGC[C/G]CAGCTAATTTTTTTG | 10055 |
| rs555803413 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47154179 | CACTGCAACCTCCAC[C/G]TCCTGGATTCAAGTG | 10055 |
| rs555822939 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47179020 | GACACGGTGAAACCT[C/T]GTCTCTACTAAAAAT | 10055 |
| rs555844124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47160505 | GTTCATGCCGTTCTC[C/T]TGCCTCAGCCTCCCG | 10055 |
| rs555910583 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47170238 | CTTTTTTTGAGACAG[A/C]GTCTTGCTCTGTCAC | 10055 |
| rs555947323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47202554 | ACCTCCCAAAGTGCT[A/G]GGATTACAGGCATCA | 10055 |
| rs555951980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47201981 | GACCTTGATAAGCAG[A/G]AAGATGTTACCCCTG | 10055 |
| rs555983920 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209395 | TGCAACGAAGGAGGT[A/G]GTGCCGACGTGCTGC | 10055 |
| rs556018596 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209908 | TTTGGGAGAAAGGAG[A/T]TGCTACCAAGTCTTG | 10055 |
| rs556162531 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47204253 | CCCAGGCTGGAGTGC[A/G]GTAGCACGATCTCAG | 10055 |
| rs556401199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47168358 | CACCCAGGCTGGAGT[A/G]CAGTGGTACGATCTG | 10055 |
| rs556416355 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47134570 | AGAGGATTTATGTGA[G/T]TTGGAGGAAACTTTG | 10055 |
| rs556458897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47134112 | GTGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 10055 |
| rs556481998 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190345 | GCAGTCAACAGTGGT[A/T]TGTGTGCGTGTTTGG | 10055 |
| rs556482067 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47136571 | CGTGATCTCAGCTCA[A/C]CGCAACCCTTGCCTC | 10055 |
| rs556488922 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47177103 | ATCTTAACTTGCTCA[A/G]TCTCTGTTCTGATGA | 10055 |
| rs556514805 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47142618 | CCATTGCATGTAAGA[C/G]CCTTCATGATGTGGC | 10055 |
| rs556541332 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47196902 | AAATAAAAAAAGGTG[A/G]CCAGGTGCCGTGGCT | 10055 |
| rs556543457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47148943 | TTTTTTAAAAGTTCA[C/T]TTCAAGCATTCTTAA | 10055 |
| rs556599461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47136138 | TAAACATGGGATTTA[C/T]TGCAGTTTTTTTTCT | 10055 |
| rs556635020 | snp | C/T | 3.29527e-05 | 0.00405898 | synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47169904 | GAAGCGCACGACCTC[C/T]GACTACTTTCTCCTT | 10055 |
| rs556671038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47161352 | TGCACAAAAGAAGAT[A/G]TGCAGCATCAATGCA | 10055 |
| rs556744124 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47149684 | TTTATAAACACAAGG[G/T]GGTGCTCTTTAACCA | 10055 |
| rs556758820 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SAE1 | GRCh38.p7 | 19:47182505 | TGTGTGTGCGCGCAC[A/G]CACGCGCGCGCGCAC | 10055 |
| rs556898103 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47155457 | TGTAGGCTCTGTCCC[A/C]AACTTTTTTTTTTGT | 10055 |
| rs556902611 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47198187 | CAATCTCAACTCACC[A/G]CAACTTCTGCCGCCT | 10055 |
| rs556992573 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47163662 | AACTTGGGAGGCAGA[C/G]GTTGCAGTGAGCCAA | 10055 |
| rs557003007 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47151143 | GGGTTGGGTAGTTTT[C/T]TTTTTTTGCACCTTT | 10055 |
| rs557040044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47150689 | AGAATCTTTGCACAT[A/G]ACTTTAATCCATGTT | 10055 |
| rs557040079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47157663 | CTTTGCCCACCATTC[C/T]GGAGGGCCCTACAGG | 10055 |
| rs557076907 | in-del | -/T | 0.0101955 | 0.0706668 | intron-variant | SAE1 | GRCh38.p7 | 19:47171904 | GTTTTTTAAAAAGTA[-/T]TTTTTTTAATGTTAT | 10055 |
| rs557118213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47183285 | CTAGATCAGGTCTTG[C/T]CCTGTTTTCACATGA | 10055 |
| rs557121059 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47156198 | ATTGTTTGAGCCTGG[A/G]AGGTGGAGGCTGCAG | 10055 |
| rs557141370 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47143676 | GATCTGCAGATTTTG[A/T]GAGTTCCTCCTTGTG | 10055 |
| rs557181681 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47206046 | CCCCCTAAATTTTTC[A/G]TGTGGGATGGAGACT | 10055 |
| rs557201084 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47164192 | TTATTTTTTTGAGAC[A/G]AAGTCTCGATCTGTC | 10055 |
| rs557202354 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163068 | AAGTTAATGAAATGT[C/T]AATCCTACTACCAAA | 10055 |
| rs557218582 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47206702 | AGGGTCTAAGAGTTC[C/T]ACCTGTGTACTGTTG | 10055 |
| rs557235703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47170376 | TGCACCACTGCGCCC[A/G]GCTAATTTTTGTATT | 10055 |
| rs557248012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47146685 | AAGAAAAGTACTGGC[C/T]CATCCAAGGCCCCAG | 10055 |
| rs557258542 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47186055 | GACCAGCCTGGCTAA[C/T]ATGGTGAAACCCCGT | 10055 |
| rs557311020 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47165250 | ACATGCCACCATGTC[C/T]GGCTAATTTTTATAT | 10055 |
| rs557320114 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47199938 | TTAGATGATGGCTTT[G/T]TTTTTTTTTGGAGAC | 10055 |
| rs557321269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47138016 | TTACAGGCGTGAGCC[A/G]CTACACCCGGCCTAT | 10055 |
| rs557324023 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47137862 | GCCTCTGGAGTAGCT[C/T]GGATTACAGGCGCGT | 10055 |
| rs557325134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47191996 | GAGGCGGAGCTTGCA[A/G]TGAGCCGAGATCGCG | 10055 |
| rs557331594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47138331 | TTACAGGCATGAGCC[A/G]CTGCGCCTGGCCAGA | 10055 |
| rs557343996 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47207443 | CCGTTAAACCCTGCC[C/G]TGGCAGCTTGCCTAG | 10055 |
| rs557357059 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SAE1 | GRCh38.p7 | 19:47200692 | TAATTTGGAATAGCC[C/T]TTGGCAAACTGGCTT | 10055 |
| rs557360665 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47171513 | CAGGAGAGCAGTGGC[A/G]TGATCTTGGCTCACT | 10055 |
| rs557389206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47198744 | GCAAACCCCACTCCA[C/T]TTAGGGCCAGCAGTG | 10055 |
| rs557480913 | in-del | -/A | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191319 | GTGAGACTCCATCTC[-/A]AAAAAAAAAGAAGAA | 10055 |
| rs557481170 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | SAE1 | GRCh38.p7 | 19:47172105 | TGTATTTTTAGTAGA[A/C]ACGGGGTTTCACCAT | 10055 |
| rs557547945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47166214 | TGAGCTGGGTAGCTA[C/T]ACTCAAGTGCAGAGC | 10055 |
| rs557611657 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47131908 | GTTTCGCCATATTGA[C/G]GAGACTGGTCTCGAT | 10055 |
| rs557629223 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47187297 | TTCTGCACCCTAGCC[C/T]TCAGATGCAACGGTG | 10055 |
| rs557648651 | snp | A/G | 0.000769527 | 0.0196003 | intron-variant, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47131093 | TTCTGAGGCGTTTGC[A/G]GCCCGGAAGGAGCGG | 10055 |
| rs557664157 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47140207 | CACCTCCCGGGTTCA[C/T]GCCATTCTCTTGCCT | 10055 |
| rs557695530 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47198114 | CAATCTCTCTCTCTC[-/T]TTTTTTTTTTTTGAG | 10055 |
| rs557851837 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47165322 | CTCGAACTCCTGACC[G/T]CAGGTGGTCTACCCA | 10055 |
| rs557865319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47158419 | TTGAGACGGATTTCG[C/T]CACAATCAGGTCTCG | 10055 |
| rs557925600 | snp | A/C | 0.0337553 | 0.125452 | intron-variant | SAE1 | GRCh38.p7 | 19:47140636 | TACAAAAAAAAAAAA[A/C]AACCCATAAATCAGC | 10055 |
| rs557972431 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47154280 | ATTTTTAGCAGAGAC[A/G]GGGTTTCACTATGTT | 10055 |
| rs557974332 | in-del | -/TTC/TTCT | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129822 | TCTTTCTTTCTTTCT[-/TTC/TTCT]TTTTTTTTTTTTTTT | 10055 |
| rs557999506 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47145527 | AGGCTCATCTTCAAG[C/G]TGAAAATAAGTGCTG | 10055 |
| rs558120149 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47210001 | GGGGCTTCAGGGCTA[A/G]GAGGGAGGAGCCTGC | 10055 |
| rs558135863 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47173548 | AATCAGGATTTCCTC[A/C]CTTCAGCACACTACT | 10055 |
| rs558147420 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47183155 | TCTTGACCTCAGGTG[A/T]TCCACCCACCTTGGC | 10055 |
| rs558178115 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47167340 | GGCACGATGGGTTCA[C/T]GCCATTCTCCTGCCT | 10055 |
| rs558200802 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209403 | AGGAGGTGGTGCCGA[C/T]GTGCTGCTTCCCATC | 10055 |
| rs558213711 | in-del | -/AGA | 0.0126979 | 0.078662 | intron-variant | SAE1 | GRCh38.p7 | 19:47149627 | GTTACAAATTTGCAT[-/AGA]AGAAGAAAGCATGGA | 10055 |
| rs558228799 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47181676 | TAGAGATGGGGTTTC[A/G]CCATGTTAGCCAGGC | 10055 |
| rs558268440 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47173130 | GCCTCCTGGGTTCGA[C/G]CGATTCTACAGGCAC | 10055 |
| rs558272885 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47133809 | GAGAGCTGTAGGTTT[-/G]GTGGGGTCGGGGAAG | 10055 |
| rs558300329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47141630 | GAGGAAATGGCATTG[A/G]AGTTGGGTTTTGAAG | 10055 |
| rs558307130 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47179971 | GAATCAAGTTTTCTT[A/C]TTGTCAGAAAAGGGT | 10055 |
| rs558374171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47202728 | ACCATCCTGGCCAAC[A/G]TGGTGAAACCCCGTC | 10055 |
| rs558375971 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47169237 | ATGAATACAGCCAGA[C/G]GTTTTTTAGTTTTGT | 10055 |
| rs558410994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47203292 | CATTTGTCTGGGAAT[A/G]GCATATAGAACCCAC | 10055 |
| rs558415481 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47175202 | TTGGGGGATATCCAA[C/G]TTGAGTGGTAAACTT | 10055 |
| rs558435987 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47160040 | AAGTAACCTTTGTTA[A/C]CAATGAAATGAATTA | 10055 |
| rs558507117 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47196286 | GTGATCCTCCCACCT[C/T]GGCCTCCCAAAGTGC | 10055 |
| rs558519552 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47196948 | AGCACTTTGGGAGGC[C/G]GAGGCGGGCGGATCA | 10055 |
| rs558580825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47204299 | ACCTCCCGGGTTCAC[A/G]CCATTCTCCTACCTT | 10055 |
| rs558592388 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47145389 | TGACCTCAGGTGATC[A/C/T]GCTGGCCTCGGCCTC | 10055 |
| rs558775724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47135325 | CTCCTTCCCCTCCAC[C/T]CCCCACTACCCTTCC | 10055 |
| rs558792596 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47162407 | AGCTTTACCAGACCC[C/T]GTTAAGTTACTCTCA | 10055 |
| rs558864575 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129766 | TTTTTTTCCCTTCCT[C/T]CCTTCCTTTCCCTCT | 10055 |
| rs558903110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47136187 | TCTGTTGCCCAGGCT[A/G]GAGGACAGTGGCACG | 10055 |
| rs558981014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47163075 | TGAAATGTTAATCCT[A/G]CTACCAAATGATAAC | 10055 |
| rs558986618 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47149852 | GGAGGCTGAGGCAGG[C/T]GGATCACGAGGTCAA | 10055 |
| rs559021553 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47191065 | CAGTACTTGGGAGTT[A/C]CAGTGACCAAGTCAT | 10055 |
| rs559027457 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | SAE1 | GRCh38.p7 | 19:47168221 | TAAAACAAAAAACTG[-/T]TTTTTTTGTATGTGT | 10055 |
| rs559060878 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47132856 | GATCACACCACTACA[A/C]CCCAGCCTGGGTGAC | 10055 |
| rs559098222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47170062 | TCAGTGATCACTTGA[A/G]AAAGGGGTGGTCACT | 10055 |
| rs559152528 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47175988 | TTGAAGGCAGAAAAA[A/G]TTTTCTTTGTTAAAC | 10055 |
| rs559160496 | in-del | -/TC | | | intron-variant | SAE1 | GRCh38.p7 | 19:47140118 | AATTTTTTTTTTTTT[-/TC]TTTTTGAAACAGACC | 10055 |
| rs559169740 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47155749 | GCCCGGCCCCATACC[C/G]TTTTTTTTTTTTTTT | 10055 |
| rs559180410 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47207029 | GACTGGGTGCAGTAG[A/C]TCATGCCTGTAATTC | 10055 |
| rs559193205 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47150737 | CCGAAAACTTAACAA[C/G]TTGGTGATTAATTTC | 10055 |
| rs559201061 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191620 | ACAGTGGCAGGAACC[C/G]TGTGCTAGATGACTC | 10055 |
| rs559206319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47162692 | TACTGTTAGGCCTGA[C/T]TTAAGAAGTAAAATA | 10055 |
| rs559232715 | snp | A/G | 0.000360097 | 0.0134134 | intron-variant | SAE1 | GRCh38.p7 | 19:47150168 | ATTTTCCCTAAAAAT[A/G]CAAGACTTAAAAAAA | 10055 |
| rs559262025 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47150496 | TTCTGAGCTTTTTCC[C/G]AAGAAAATGTATAAG | 10055 |
| rs559282942 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47205403 | ATCTAACTTTCTTCT[A/G/T]TGTAATGGGCACCGA | 10055 |
| rs559322422 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47166974 | TTTTTTTTTTTGAGA[C/T]GGCGTCTCACCTTGT | 10055 |
| rs559449316 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47154231 | GAGTAGCTGGGACTG[C/T]AGGCACCCGCCACCA | 10055 |
| rs559469283 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47184752 | GAGAGCTCAGTCTGA[A/C]TGTAGGATATGACAT | 10055 |
| rs559489859 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47137351 | CAAGGTCACACTATC[A/G]CACTCCAGCCTGGGT | 10055 |
| rs559500617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47192367 | GCGACTCCTGCCTCA[A/G]GCTCCCGAGTAGCTG | 10055 |
| rs559502696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47199460 | CGAGACTGAGACATG[A/G]AAAAGCGGTTTCCCC | 10055 |
| rs559503171 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47131235 | TTGGGAGGGCCGTTC[A/C/T]GAAGGATGGGAGCTC | 10055 |
| rs559539356 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SAE1 | GRCh38.p7 | 19:47149475 | CGTGCCCTGCCCACA[C/G]TGGTCTAGTTTTAAA | 10055 |
| rs559541363 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47200006 | CATGATCTTGGCTCA[A/C]TGCAAGTTCCGCCTC | 10055 |
| rs559579273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47141793 | AAATTATTCTTAGTT[A/G]TTACTAAATCCTTTT | 10055 |
| rs559589272 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47177503 | AGCTGGGACTACAGG[A/C]GTGTGCCACCATGTC | 10055 |
| rs559595761 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47153383 | AGAACAAACAGACCT[C/T]ATCCTCTCATTTTGA | 10055 |
| rs559604776 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47165643 | GCATTGTCGGGTGTA[G/T]TTTTTCTTTATAAGC | 10055 |
| rs559642066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47198266 | AGGTGCCTGCCACCA[C/T]GCCCAGCTAATTTTT | 10055 |
| rs559724217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47193559 | GGGTGCTGTGGCTCA[C/T]GCCTGTAATTCCAGC | 10055 |
| rs559728583 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191441 | ACGCTAGTCCTGTCA[G/T]TCACTCCTGAGAGAA | 10055 |
| rs559745326 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47158597 | GAGCAGTGCTCTGTC[C/G]GAGGAAGTAGGATAA | 10055 |
| rs559798471 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167797 | AGAGACACAGAGTCT[A/G]TACCACGCCTGGCCT | 10055 |
| rs559859777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47171099 | TCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTG | 10055 |
| rs559862581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47186778 | GTTTCATTGCAAAGA[C/T]GAAAGCGTGGGCAGG | 10055 |
| rs559871779 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47199466 | TGAGACATGGAAAAG[C/T]GGTTTCCCCAAAGAG | 10055 |
| rs560052027 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant, missense, intron-variant | SAE1 | GRCh38.p7 | 19:47130865 | CCGGCGGCGGTAGGT[A/G]GCGCGCGGGTCCGGC | 10055 |
| rs560083974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47132307 | CCAGTGGAGTGCAGT[A/G]GTGGGATCACAGCTC | 10055 |
| rs560099654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47186488 | TACCACATTTTTACA[C/T]GGTTCATTGAGCATT | 10055 |
| rs560218131 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47138777 | CACTTGAGCCAGGCA[A/G]TTGAGACTAGCTTGG | 10055 |
| rs560262069 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47145208 | GGTTTCTCCATGTTG[G/T]TCAAGCTGGTCTTGA | 10055 |
| rs560300595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47144567 | AGCAGGGCTTGGTGG[C/T]GGGCGCCTGTGGTCC | 10055 |
| rs560304120 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47208674 | AGGTGATCCGCCCAC[G/T]TCAGCCTCCCAGAGT | 10055 |
| rs560334026 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47153563 | CAAAACCCTCCAACT[G/T]GCTAATTGAGAGGGA | 10055 |
| rs560347954 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47173153 | ACAGGCACGCACCAC[A/C]ACACCCAGCTAATTT | 10055 |
| rs560377878 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47140730 | AACCTGGGAGGTTGA[G/T]GCTGCAGCGAGCCCT | 10055 |
| rs560424885 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47146848 | TGGCTGGTGGACTCC[A/G]GAGACAGCACACAGA | 10055 |
| rs560464736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47172847 | TGCTCTGTGCCGGGC[A/G]TTTTCCATGTATATC | 10055 |
| rs560479542 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47174733 | GCCCGCCACCATGCC[C/T]GGCTAATTTTTTTGT | 10055 |
| rs560485146 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47194655 | TTTCCTTGGGCAGTA[C/T]GTAGGGAACAAGAAT | 10055 |
| rs560494806 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47177754 | ACTGAAGGTCTGACC[A/G]TCTTTGGGGAGTTGT | 10055 |
| rs560510714 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47134340 | TTCAGAAGGTTTTAG[A/G]GGGTGCAGTGGTGGG | 10055 |
| rs560556117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47202809 | CAGCTACTCAGGAGG[C/T]TGAGGCAGGAAAATG | 10055 |
| rs560588870 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | SAE1 | GRCh38.p7 | 19:47137231 | CTCTACTAAAAATAC[-/A]AAAAAAATTAGCCAG | 10055 |
| rs560588962 | in-del | -/GAAAA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47193850 | AAAAAAGAAAGAAAA[-/GAAAA]AGAAAAAGAAATTAC | 10055 |
| rs560601891 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47134922 | GATTGGCTGGGGGTT[C/G]CAGGAGGGAGGGAAG | 10055 |
| rs560620784 | snp | A/G | 1.6582e-05 | 0.00287936 | intron-variant | SAE1 | GRCh38.p7 | 19:47152870 | AGTTTGCAAAACTCA[A/G]ACCCAGCCAATTTCT | 10055 |
| rs560638737 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47168108 | TGAGGCACGAGAATT[G/T]CTTGAACCCAGGACA | 10055 |
| rs560681976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47201124 | TTGGCTCACTGCAAC[C/T]TCCGCCTCTGTGCTC | 10055 |
| rs560743229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47180517 | GTTTGCGGTGAAACA[A/G]TGTAGATGTTTCCTT | 10055 |
| rs560808424 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47187943 | TGGGGCAAGCCCTGT[G/T]CCAGGTGTTCAGTAT | 10055 |
| rs560848121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47173988 | ACGGGGTTTCACCGC[A/G]TTAGCCAGGATGGTC | 10055 |
| rs560852912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47154316 | TGCTGGTCTTGAACT[C/T]CTGACCTCAGGTGGT | 10055 |
| rs560863629 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47161581 | TCCTGTTTTATCACG[G/T]GTTTATAAATCTAAA | 10055 |
| rs560949857 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47191204 | TCACTTAAGGTCAGA[A/C]GTTCGAGACCAGCCT | 10055 |
| rs560951673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47182701 | CCGACTCTGCTCCTC[A/G]GTCTGCAAGAGAGGT | 10055 |
| rs560962672 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47148697 | TGGGCTCAATGCAGC[A/G]TCTGCCTCCCAGGTT | 10055 |
| rs561067642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47181770 | AAGTGTGAGCCAGTG[C/T]ACCTGGCCTCTTTTT | 10055 |
| rs561076862 | snp | C/T | 0.0003954 | 0.014055 | intron-variant | SAE1 | GRCh38.p7 | 19:47203643 | TCTGTTCCCAGTGCT[C/T]CATTTTCCTTGTCTT | 10055 |
| rs561116079 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129274 | GTCTCTACTAAAAAT[A/G]CAAAAGTTAGGTGGG | 10055 |
| rs561144883 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SAE1 | GRCh38.p7 | 19:47159797 | CTCCTGGGTTCAAGC[A/C]ATTCTCCTGCCTCAG | 10055 |
| rs561158308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47197010 | ACATGGTGAAAACCC[A/G]TCTCTACTAAATATA | 10055 |
| rs561205684 | snp | A/G | | | intron-variant, missense | SAE1 | GRCh38.p7 | 19:47205120 | TTCTTGGCTGCCTTC[A/G]TGGACTCCGGTGAGG | 10055 |
| rs561254638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47136224 | GCCCAGTACAATCTC[C/T]ACCTCCCAGGTTCAA | 10055 |
| rs561271426 | snp | C/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47210051 | TCACATGCGGCTCAA[C/G]TCACTCAGAGGCTGT | 10055 |
| rs561275109 | in-del | -/AGTG | 0.00478085 | 0.0486577 | intron-variant | SAE1 | GRCh38.p7 | 19:47138800 | TAGCTTGGGCAACTT[-/AGTG]AGGCCCCATTTCAAT | 10055 |
| rs561303199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47143294 | TATTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT | 10055 |
| rs561335939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47205528 | GTTTATATGCCCAAT[C/T]TGAGAAGAGGGTAAT | 10055 |
| rs561416344 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47187767 | CCTCAGTTGATCTGC[C/T]TGCCTTGGCCTCTCA | 10055 |
| rs561445047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47149297 | TGCCTCAGCCTCCTG[A/G]GTAGCTGGGATTACA | 10055 |
| rs561581570 | snp | A/C | 0.00279162 | 0.0372561 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129859 | TCTTGCTCTGTTACC[A/C]AGGTTGGAGTGCAGA | 10055 |
| rs561584808 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47138105 | CTGGAGTGCAATGGC[A/G]TGATCTAGACTCACT | 10055 |
| rs561623573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47137495 | TATTGATAGTTGACA[A/G]TTACAACTAAAATTT | 10055 |
| rs561641252 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47156447 | CGGCAACACTGCACT[C/G]CAGCCTGGCGACAGA | 10055 |
| rs561698248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47165727 | AGATTAGGCAGCTTG[A/G]TTAAGTTTTGTTTTG | 10055 |
| rs561710171 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47198304 | TTTTAGTAGAGATGG[G/T]GTTTTCCATGTTGGC | 10055 |
| rs561745607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47157139 | AGGCGGCGTTGGAGA[C/T]TTTCTTTCTCATTTT | 10055 |
| rs561758483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47138148 | TCCCGGGTTCAGGCA[A/G]TTCTCCTGCCTCAGC | 10055 |
| rs561761205 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SAE1 | GRCh38.p7 | 19:47150827 | AAAAGCACACCTGAT[C/T]TTGATCTATGTCTGT | 10055 |
| rs561780732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47164254 | GCTCACTGCAAGCTC[C/T]GCCTCCTGGGTTCAC | 10055 |
| rs561825160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176769 | GTGGCCAGACTGTAC[A/G]CTTCCTGCTGCATTT | 10055 |
| rs561831485 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47180821 | GACTTTGTCTCCCCC[A/G]AAAAAGAAGATGCTT | 10055 |
| rs561867264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47185597 | AGGCTGAGCTACTGC[A/G]CCCAGCCTATTTTTG | 10055 |
| rs561882799 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47135466 | ATTTCACTTAACATA[A/G]TAACATCCAGTGCCC | 10055 |
| rs561893266 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47183887 | CTGCTTGTGACCAGG[C/T]AGGGTGGCTCTGAAT | 10055 |
| rs561948135 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47207429 | GGTGCTCCTGGGAAC[C/T]GTTAAACCCTGCCCT | 10055 |
| rs562017539 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47143819 | TAGAGACTCACACCC[C/G]CTCATTGAGCTTGCC | 10055 |
| rs562036339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47172148 | GGCCTCAAACTCCCA[A/G]CCTCAGATGATCCAC | 10055 |
| rs562057686 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47158627 | AACCGAAAGACGGAC[A/G]TAGGGGCAGAGTTGC | 10055 |
| rs562062677 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47174399 | ACAATGTTTTATTTT[A/G]TTTTGTTTTTTTCTG | 10055 |
| rs562076791 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47208063 | AAGCCTAGCGACTCT[A/G]TGTCCTCATGGAATA | 10055 |
| rs562118264 | snp | C/G | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47193725 | CCCAGTTACTTGGCA[C/G]GTTGAGGCAGGAGAA | 10055 |
| rs562147805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47187553 | TCTGAGCCAGGGTCT[C/T]GCTTTGTCACCCAGC | 10055 |
| rs562185549 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47152733 | ATTGAAACCTGCAAC[G/T]TTTCTTTTGTCTTCT | 10055 |
| rs562229819 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47195211 | AGGTGCCTGCCACCA[C/T]GCCTGGCTAATTTTT | 10055 |
| rs562236740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47171712 | CAGGTGATCTGCCCA[C/T]CTCAGTCTCCCAAAG | 10055 |
| rs562280067 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47186830 | GCATTTCAGAGTAGT[C/T]TTCATGGGCGGCCAC | 10055 |
| rs562318208 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209666 | TTGGACTTATTCCCC[A/T]CCTGATACCTTATAG | 10055 |
| rs562321478 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SAE1 | GRCh38.p7 | 19:47193040 | TCTGGCATCCAGATC[A/G]TCTAGATGGTCACAG | 10055 |
| rs562383209 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47152183 | ATGATCACAAAGCTT[A/C]TCCCGAAAAGATGGT | 10055 |
| rs562417003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47208561 | TTCTCCTGCCTCAGC[C/T]TCCCGAGTAGCATGC | 10055 |
| rs562466806 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47167099 | TGGGATTACAGGTGC[C/T]TGCCACCACACCCAG | 10055 |
| rs562490537 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47164344 | CGGCTAATTTTTTGT[A/G]TTTTTAGTAGAGACG | 10055 |
| rs562504147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47140452 | AGATGGGGTTTCACC[A/G]TGTTGGCCAGGCTGG | 10055 |
| rs562542969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47139792 | ATTTTTAGTAGAAAC[A/G]GGGTTTTACCATGTT | 10055 |
| rs562666527 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47173199 | AGGCAGGGTTCCACC[A/G]TGTTGGCCAGGCTGG | 10055 |
| rs562753319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47195031 | TACAGACGTTACAGA[C/T]GTGAGCCACCACACC | 10055 |
| rs562784037 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47147823 | GAGTGCAGTGGCGCG[A/C]TCTTGGCTCACTGCA | 10055 |
| rs562827299 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47144311 | TGCACTCCAGCCTGG[A/G]CAACAGAGTGAGACT | 10055 |
| rs562876534 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SAE1 | GRCh38.p7 | 19:47196069 | TTTTTTTTCCCAGAC[A/G]GAGTCTCGCTCTGTT | 10055 |
| rs562905429 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47174797 | CCAGGATGGTCTCGA[C/T]GTTCTGACCTCGTGA | 10055 |
| rs562912805 | in-del | -/AAAC | 0.00557542 | 0.0525036 | intron-variant | SAE1 | GRCh38.p7 | 19:47168403 | CGACCTCCTGTGCTA[-/AAAC]AGTTCTCTTGCCTCA | 10055 |
| rs562949382 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47154511 | TTTTTTTTTTTTTTT[C/T]TGAGACAGACTTTCA | 10055 |
| rs562988068 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SAE1 | GRCh38.p7 | 19:47160616 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG | 10055 |
| rs563006929 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129061 | CTGACCTCGTGATCC[A/G]CCCACCTCTGCCTCC | 10055 |
| rs563074446 | snp | C/T | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129936 | ATTATCCTACCTCAG[C/T]CTTCCAAGTAGCTGG | 10055 |
| rs563075169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47181907 | CTCCTGGACTCAAGC[A/G]ATCCTCCCACATCAC | 10055 |
| rs563184687 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47150068 | GGTGACAGAGCAAGA[C/G]TGTCTCAAAAAAAAA | 10055 |
| rs563223152 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SAE1 | GRCh38.p7 | 19:47156370 | TGTAGTCCCAGCTAC[G/T]TGGGAGGCTGAGGCA | 10055 |
| rs563234440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47189301 | AGTGGCTCACGCCTG[C/T]AACCCCAGCGCTTTG | 10055 |
| rs563248406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47162598 | TCCCTCTACCCTCCC[C/T]ACCCCCTACCCCAGG | 10055 |
| rs563259541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47155710 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGCGTGA | 10055 |
| rs563267952 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47168582 | TACAAAAGTGAGCCA[C/T]CACACTCAGCCATAA | 10055 |
| rs563288393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47204420 | AGCCAGGATGGTCTG[A/G]ATCTCCTGACATCGT | 10055 |
| rs563303449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176859 | ATTCTCCCATGGCAT[A/G]TTGCAAAACAGTAAG | 10055 |
| rs563388266 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47169404 | GCGGCCGCCAGCATG[C/G/T]CTAGCTAATTTTTGT | 10055 |
| rs563438925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47176416 | ACCTAAGAATATCTC[A/G]CAAAGAAACCTGATT | 10055 |
| rs563440892 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47184662 | GTGATCCACCCACCT[C/T]AGCCTCCCAAAGTGC | 10055 |
| rs563477348 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47183803 | GGGTTGGCAGAGAGC[A/C]GCAGATGCCTAGAGT | 10055 |
| rs563486477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47197623 | TCAAGGCAATGTAAG[A/G]TCTGTAAACATTATT | 10055 |
| rs563486569 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47140352 | ACCTCGTGATCTGCC[C/T]GTCTCGGCCTCCCAA | 10055 |
| rs563520008 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47206376 | CGGGGCCTGCAGTCC[A/G]AGGGCCTCAGACTCA | 10055 |
| rs563525958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | SAE1 | GRCh38.p7 | 19:47205129 | GCCTTCGTGGACTCC[A/G]GTGAGGCTTTTTCCT | 10055 |
| rs563554455 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47207016 | TAAATGTTCCCTTGA[C/G]TGGGTGCAGTAGCTC | 10055 |
| rs563625886 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190573 | TGGCTGGACTGATTG[A/G]CCCCCTTCCCAGAGG | 10055 |
| rs563705032 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129958 | AGTAGCTGGGACTAC[A/G]AGTGTGAGCCACCAT | 10055 |
| rs563773538 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47136302 | TGCCACCACGCCCGG[C/G]TAATCTTTGTATTTT | 10055 |
| rs563790923 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47199305 | CAGGAGAATGGCGTG[A/T]ACCCGGGAGGCAGAG | 10055 |
| rs563875240 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47186631 | CGTTTCTGAGAAAGT[G/T]CATGCTCCTTTTCCC | 10055 |
| rs563917321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47157237 | CTATTCACAGAACCA[C/T]AATTATCCAGAGTGA | 10055 |
| rs563971568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47132189 | GCTGGTCTCAAACTC[C/T]GGACCTCAAGTGATC | 10055 |
| rs563982976 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47171687 | CAGGCTGGTCTCGAA[C/T]TCCTGACCTCAGGTG | 10055 |
| rs563991827 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47164369 | GAGACGGGTTTCACC[A/G]TGTTAGCTAGGATGG | 10055 |
| rs564030753 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47170709 | AGCGAAGTTTCTCCA[C/T]GTAGCCAGGCTGGAC | 10055 |
| rs564118031 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47192341 | CTGCAACCTCTGCCT[C/G]CTGGGTTTGAGCGAC | 10055 |
| rs564140881 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47173660 | CACTAGATGCCAGTA[A/G]TATCTCCCCACCCAG | 10055 |
| rs564186965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47157835 | GGCATTCAGTGCATT[C/T]CTGCTGACAATCCCT | 10055 |
| rs564228738 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SAE1 | GRCh38.p7 | 19:47145128 | CTGCCTCAATCTCCC[C/G]AGTAGCTGGGATTAC | 10055 |
| rs564235274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47172240 | ACTATTTGAAAGTCC[C/T]GAATATCCATTTGTG | 10055 |
| rs564250711 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47173425 | TGTCCAGTAGCACCT[A/G]CACTGAATATTCACT | 10055 |
| rs564259115 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47171238 | TCAGCCCCCCAAAGT[A/G]CTGTGATTACAGGTG | 10055 |
| rs564273756 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47180458 | ACCATAGTAGTAACA[A/G]TTGTTTCAATCAAGA | 10055 |
| rs564338965 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47142801 | TTGCTCATATGGCAT[C/T]TCCTCAGAAAGGCTT | 10055 |
| rs564370932 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47159466 | TCCAGTGTGTAGCAC[A/C]GTCATATCCACGGAA | 10055 |
| rs564371843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47178556 | TCAGCTCATTGCAAC[C/T]TCCGCCTTTTGGATT | 10055 |
| rs564372170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47146778 | ACTATGGACCACTCT[C/T]ATGGAAATAGCAAGG | 10055 |
| rs564407267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47166608 | ACATATTAGTTGGTT[C/T]GTTGCTTATAGTCAG | 10055 |
| rs564409543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47177929 | GGAGAGAGCAGGCTA[A/G]TGGTTTCCCTATTGA | 10055 |
| rs564410473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47153318 | GGAGGCATATTCAAC[C/T]AAAGTCTACCTTGGA | 10055 |
| rs564446165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47152776 | CAAAGAACCTGTTGT[A/G]CCAGTTTGAAACATG | 10055 |
| rs564489010 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47201039 | TTTTTTTTTATTTTT[A/T]TATTTTTTTTATTTT | 10055 |
| rs564501899 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47173894 | GGTTCACGCCATTCT[C/T]CTGCCTCAGCCTCCC | 10055 |
| rs564517731 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47140640 | AAAAAAAAAAAAAAC[C/G]CATAAATCAGCCAGG | 10055 |
| rs564534331 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SAE1 | GRCh38.p7 | 19:47194544 | GGCTTGGGCCTAGAA[G/T]CTGATCCATGTCTCT | 10055 |
| rs564586839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47158662 | GCTGCCCTCACTGCC[A/G]CAGCCAGCTCCTTCC | 10055 |
| rs564594508 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47172842 | GGACTTGCTCTGTGC[C/T]GGGCGTTTTCCATGT | 10055 |
| rs564632909 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47173309 | GCCCAAAGTCTTGTT[C/T]GGAACAACCATGCAC | 10055 |
| rs564637131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47180955 | CTTGGAATATGTAAC[C/T]CTGGGTTGGATCTGA | 10055 |
| rs564642244 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47178043 | GTCAAGAGATCGAGA[C/T]CATCCTGGCCAACAT | 10055 |
| rs564712536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47186999 | TGGGTCCCCACCACA[A/G]CTAGCATAGGGTAGG | 10055 |
| rs564719343 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47202975 | CTGTAGGGAGGCTTT[C/T]CCTTTCACTTGTCTG | 10055 |
| rs564719590 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47195275 | GGCCAGGTTGGTCTC[A/G]AACTCCTGACCTCAG | 10055 |
| rs564723882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47202044 | CAGGGCGTAAGGAGC[C/T]GGAGGTGCCTTTGGA | 10055 |
| rs564733013 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47140007 | CAATGGTGCGGTCTC[A/G]GCTCACTGCAACCTC | 10055 |
| rs564755606 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47203602 | AGAGCCTACTACTGA[A/G]TTTCTCCAGATGTCA | 10055 |
| rs564852204 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47194771 | TTTTTTTTTTTTGAG[A/G]TGGAGTTACGCTCTA | 10055 |
| rs564860373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47167508 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGTGTGA | 10055 |
| rs564891482 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47164048 | TTTTGGGATTACAGG[C/T]GTGAGCCATTGCACC | 10055 |
| rs565017002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47160684 | ACAGGCGTGAGCCAC[C/T]GTGCCCAGCCTAATT | 10055 |
| rs565051690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47168054 | AAAAATTAGCTGGGC[A/G]TGGTGGCATGCATCT | 10055 |
| rs565083008 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47196245 | TTTCACCATGTTGGT[C/T]AGGCTGGTCTCAAAC | 10055 |
| rs565121549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47154621 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGATTACA | 10055 |
| rs565126912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47135106 | TTGATACAGGCATAC[A/G]ATGGGTAATAATCAC | 10055 |
| rs565152905 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129173 | TGGTGGCTCACACCT[A/G]TAATCCGTGCACTTT | 10055 |
| rs565165351 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47142023 | TGACCTCAGAGAAGT[C/G]TTGGGATGGCCTGAC | 10055 |
| rs565253048 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190479 | TTTCTTCCTGCCCCC[C/G]TCCACTGCTGCTAAC | 10055 |
| rs565272598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47142754 | TCTGCTGCCAAATAT[C/T]TGTGTGTTTGTCCTT | 10055 |
| rs565316816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47180492 | AAAGTGCTAAAATCA[A/G]TGGGGAACAGTTTGC | 10055 |
| rs565355645 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47179048 | AATACAAAAATTAGC[C/T]GGGCGTGGTGGCGGG | 10055 |
| rs565385926 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47147893 | CCTCCCTAGTAGCTG[C/G]GACTACAGGCGCCCA | 10055 |
| rs565387720 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47155032 | ACCACCATCCCGATC[G/T]GTGACCTGGAGAGGC | 10055 |
| rs565431873 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SAE1 | GRCh38.p7 | 19:47151525 | CGCCCAGGCTGGAGT[A/G]CAGTGGCATGATCTT | 10055 |
| rs565435472 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47169497 | GTGATCCGCCTGCCT[C/T]GGTCTCCAAAGTGTT | 10055 |
| rs565510162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176531 | CATTTGCCCTATTGT[A/G]GAGGGAGAGTAGTGT | 10055 |
| rs565543417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47175751 | CAAAATAAAATAAAT[A/G]AAATATCTCTAAACT | 10055 |
| rs565606277 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | SAE1 | GRCh38.p7 | 19:47182511 | TGCGCGCACGCACGC[A/G]CGCGCGCACACCACT | 10055 |
| rs565609975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47174882 | CTGGCCACATTTTTG[C/T]ATTTTTAGTAGAGAC | 10055 |
| rs565652185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190829 | CCACTTCTCACCCAC[C/T]GAACTTACAGCTTGA | 10055 |
| rs565719862 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47151738 | CACTTTCCATTTGGA[C/G]ATAAGTCTTCATTTT | 10055 |
| rs565728598 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130064 | TAAAGTAATCTGCCT[G/T]CCTTGGCCTTCCGAA | 10055 |
| rs565769817 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47211123 | AAAGGCCAGGCGTGG[A/T]GGCTCACGCCTGTAA | 10055 |
| rs565790333 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47155276 | GGGTCAGGCAATGAC[A/C/G]ATTGAAAAGGATAAG | 10055 |
| rs565839019 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47135340 | CCCCCACTACCCTTC[C/T]TAGCCTCTGGTAACC | 10055 |
| rs565870945 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47170172 | CAAGTTGACCTTATG[C/G]TAATAGTGTTACAGG | 10055 |
| rs565893470 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129455 | GTGTGCCACCACGCC[C/T]GGCTAATTTTTTAGT | 10055 |
| rs565916889 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47141451 | CCGGCTGAATAATGA[A/G]TTTTAAACAACTGCA | 10055 |
| rs565930495 | snp | C/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47135927 | TCCTGCCTCAGCCTC[C/T]CTAGTAGCTGGGACT | 10055 |
| rs565950160 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47206487 | GGAATCATCTTTTGC[A/G]TCTTTCCTTTCTTAC | 10055 |
| rs565950735 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47191911 | ATACAAAAATTAGCC[A/G]GGCGTGGTGATGGCC | 10055 |
| rs565987408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191642 | AGATGACTCTTGTGC[A/G]ATCTTATTTCTTTGT | 10055 |
| rs566002760 | in-del | -/G | 0.0123036 | 0.0774623 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130249 | AGTAGGGACATGAAA[-/G]GCTGGGCACAGTGGC | 10055 |
| rs566007218 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47183060 | AGCTGGGATTACAGG[G/T]GCCTACCACCACGTC | 10055 |
| rs566010482 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47178989 | ACAGGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 10055 |
| rs566025414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47156711 | TTTAGTAGAGATGGG[A/G]TTCCACCATGTTGGC | 10055 |
| rs566035792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47205813 | GGTTTATAAAAGAGA[A/G]ACTAAGGTGCAGGAA | 10055 |
| rs566070021 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47140345 | TCTTCTGACCTCGTG[A/T]TCTGCCTGTCTCGGC | 10055 |
| rs566325924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47144087 | GCCTGTAATCCCAAC[A/G]CTTTGGAAGGCTGAG | 10055 |
| rs566348083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47178035 | ATCATGAGGTCAAGA[A/G]ATCGAGACCATCCTG | 10055 |
| rs566364534 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47151059 | CTTGATAAATGTGAA[A/T]TAGTCATAGATGAGC | 10055 |
| rs566399666 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47150534 | ATTGTTTAGGCTTAG[C/T]ATATTGTGTGAATGT | 10055 |
| rs566410636 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47192794 | ATCTGCCCACCTTAG[C/T]CTCCCAAAGTGCTGG | 10055 |
| rs566442501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47171984 | GAGTGCAGTGGTGCA[A/G]TCTTGGCTCACTGCA | 10055 |
| rs566473925 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47196014 | GTTGGGATTGCAGAT[A/G]TGTGCCATCACACTC | 10055 |
| rs566480532 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47171359 | AGTGCAGTGGCACGA[A/T]CTTGGCACACTGCAA | 10055 |
| rs566489118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47185964 | GCTTATTGGCCCCGG[A/G]CGTGGTGGCTCATGC | 10055 |
| rs566520770 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47208256 | TTTTAAGGTGTTTTT[G/T]TGTTTGTTTGTTTTT | 10055 |
| rs566558106 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47200341 | GGGCTCAGGCAACAC[G/T]CTCATCTCGGCCTCT | 10055 |
| rs566575448 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SAE1 | GRCh38.p7 | 19:47146044 | AGTCTTAAAGAACAA[A/G]GAGGGTTGTCAAGAT | 10055 |
| rs566575457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47139171 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 10055 |
| rs566601840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47145416 | CCTCCCAAAGTGCGG[C/T]GATTACAGGTGTGAG | 10055 |
| rs566605369 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47177376 | GTTTTTTTTCCCCCC[C/G]AAAACAGGGTCTTGC | 10055 |
| rs566611778 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47151920 | GTCCTTGCAGGTTTT[A/T]TAGTTACTTTAGACT | 10055 |
| rs566644794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47199848 | TACCATGAGATCCAA[A/G]CCTGTACAGTGTCAT | 10055 |
| rs566687270 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SAE1 | GRCh38.p7 | 19:47167113 | CCTGCCACCACACCC[A/C]GCTAATTTTTTTGTA | 10055 |
| rs566793857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47207502 | TGTGGTGAAATTTCA[A/G]TCCTTTCTGGGTTAA | 10055 |
| rs566831440 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47203752 | GAAGGTAAAACATCA[C/T]TGTGGAGCAGAAAAT | 10055 |
| rs566850776 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47187173 | TGGCAAGATGCCGTG[A/C]ATGGTTAGAGGCCAG | 10055 |
| rs566865392 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47152383 | ATAAAGTTTCACACC[A/G]CAATCTGTGGAAAAA | 10055 |
| rs566875703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47160776 | CCTTGTGATCCACCC[A/G]CCTCAGCCTCCCAAA | 10055 |
| rs566889316 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47135800 | GTACCACAATTTCTA[-/T]TTTTTTTTTTTGAAA | 10055 |
| rs566912827 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47194883 | AAGTACCTGGGACTA[C/T]AGGCGTGCGCCACCA | 10055 |
| rs566923961 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47193257 | GTAGAGATGGGGTTT[C/T]GCTGTGTTGGCCAGG | 10055 |
| rs566957686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47173037 | GTCTTGTTCTTTTTC[C/T]TTTTCCCCAGAGACA | 10055 |
| rs567011815 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47172108 | ATTTTTAGTAGAAAC[A/G/T]GGGTTTCACCATGTT | 10055 |
| rs567020386 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47203269 | GTTAACACAGGCCTG[C/G]TCCCTGACATTTGTC | 10055 |
| rs567049334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47159850 | CAGTGTGTGCCACCA[C/T]ACTCGACTGGTTTTT | 10055 |
| rs567068206 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47162913 | GGGAGGATTGCCTGA[C/G]CCTGGCAAGTGTAGG | 10055 |
| rs567078847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47133505 | GCTGTGATTACAGGC[A/G]TGAGCCACTGCGGCC | 10055 |
| rs567094132 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47179615 | CAGTGTCACGATCAT[A/T]ACTTACTGCAGCTTC | 10055 |
| rs567103883 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47154072 | CTGGGATTACACAGG[C/T]GTGAGCCACCGCACC | 10055 |
| rs567122039 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47152458 | ATCAAAAGGAGGGGG[G/T]TAAAAAGCCCTTGTA | 10055 |
| rs567164190 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47132495 | ACTCCCAAGCTCAAG[C/T]GATCCTCGGCCTCAA | 10055 |
| rs567173348 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47188211 | AAATGAACCACCAGG[C/T]ATGGTGGTGCATGCC | 10055 |
| rs567175261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47195596 | TTCTGGCTAAAGCAG[A/G]CTTTAAACTGGTCCT | 10055 |
| rs567264236 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | SAE1 | GRCh38.p7 | 19:47203089 | AATTAAGTGATTTGC[A/T]TACTAGGATGGGTAA | 10055 |
| rs567323646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47181388 | TAGCAGTACTGTTTC[C/T]ATGTTATTTATTTTT | 10055 |
| rs567375728 | in-del | -/AT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47185165 | AATGTTGCAAAAAAC[-/AT]GTGTCTAAAATCTCT | 10055 |
| rs567463118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47147266 | GCCGGAATGCAGTGG[A/G]CATGATCATGGCTCA | 10055 |
| rs567511883 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47143327 | TCAGGCTGGTCTCGA[A/T]CTCCTGACCTCAAGT | 10055 |
| rs567516908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47141437 | ATGAGTCACCGGGCC[C/T]GGCTGAATAATGAAT | 10055 |
| rs567553661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47140951 | CCTCTCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 10055 |
| rs567564903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47154684 | TATTTTTAGTAGAGA[C/T]GGGGTTTTGCTATGT | 10055 |
| rs567633035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47168863 | CCCGCCTCGGCCTCC[C/T]AAAGTGCTAGGATCA | 10055 |
| rs567669740 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47168320 | AGTCTGTATTTTTTT[C/T]TCTCTCTCTCTGTTT | 10055 |
| rs567734543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47196798 | ACAGAGGGTGTCAGA[C/T]GCCCTATTATGCTGT | 10055 |
| rs567736452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47135211 | AGTTGCTTTGAAATG[C/T]ACAACAAATTATTGT | 10055 |
| rs567749695 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47204597 | CTGCAACCTCCGCCT[A/C]CTGGGTTCAAGCGAT | 10055 |
| rs567785535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47182239 | GAAACTTCTTATTTT[A/G]GAACTTGTAACCTTT | 10055 |
| rs567799678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47155921 | AATTTTTGTATTTTT[A/G]GTAGAGACGGGGTTC | 10055 |
| rs567855443 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47155422 | TGGGATTTTTCAAGA[C/G]AATGAGAAATGCAAA | 10055 |
| rs567942985 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47155497 | ATGGAATTTTTTCTT[G/T]TCGCTCAGGCTGGAG | 10055 |
| rs567948694 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47162837 | TCTCTACCAAAAATA[C/G]AAAAATTAGCTGGGC | 10055 |
| rs567989865 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47161897 | GCTTTTAAGGAGAAG[C/G]AACACGTTTGTGAGG | 10055 |
| rs567989983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47169535 | CAGGTGTGACCCACC[A/G]CGCCTGGCCCAGTGA | 10055 |
| rs568025364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47136732 | TGACCTCAGGTGATC[C/T]GCCCGCCTTGGCCTC | 10055 |
| rs568076522 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47183232 | GTTCACGTACTTTAC[A/C]TGCATTGTGATCATA | 10055 |
| rs568111871 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47197729 | CTTTTCCACAGCTCC[G/T]TAGTATTCTAGAGTG | 10055 |
| rs568113190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190969 | TGCTGTGTCCCTGTA[C/T]GGACCTGCTGTTTCT | 10055 |
| rs568126168 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47171208 | TCACTCTCTTGACCT[C/T]GTGATCCGCCCACCT | 10055 |
| rs568163422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47149573 | ACATGCTAAGTATTT[A/G]GTCAATTCTTGCCAC | 10055 |
| rs568198589 | in-del | -/CT | 0.02016 | 0.0983543 | intron-variant | SAE1 | GRCh38.p7 | 19:47163718 | GGCGACAGAGCAAGA[-/CT]CTATCTCAAAAATAA | 10055 |
| rs568208794 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47157483 | GCCTTCTCTGATTGA[A/G]GCAGGTCTTTCACAT | 10055 |
| rs568245688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47164413 | ACCTCGTGATCCGCC[C/T]GCCTTGGCCTCCCAA | 10055 |
| rs568286555 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47178220 | TGCACTCCAGCCTGA[C/T]GACAGGGCAAGACTC | 10055 |
| rs568311909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47132309 | AGTGGAGTGCAGTGG[C/T]GGGATCACAGCTCAC | 10055 |
| rs568317196 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130245 | ACATAGTAGGGACAT[A/G]AAAGGCTGGGCACAG | 10055 |
| rs568326716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47185999 | AATCCCAGCACTTTG[A/G]GAGGCCTAGGTGGGT | 10055 |
| rs568374683 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47199530 | ACCAGCCAGCAGCTC[A/C/G]TTAGGCTGTGGCTTT | 10055 |
| rs568384041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176564 | CCACTGGAGTCCCCA[C/T]AGGGTCCTTTTGCCT | 10055 |
| rs568395978 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47151114 | CCAGTATGTTACATG[A/G]GAGGTTAGAATTTGG | 10055 |
| rs568409833 | snp | C/G | | | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210764 | AAGGATCCGTGTCTC[C/G]CCACCTTTAGTGCAA | 10055 |
| rs568418904 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47198625 | ATTACAGTGCTTGCT[C/G]TAGTAGCAGCATGCT | 10055 |
| rs568421836 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47175574 | AATCCCGTCTCTACT[-/A]AAAAAACACAAAAAT | 10055 |
| rs568450716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47207017 | AAATGTTCCCTTGAC[C/T]GGGTGCAGTAGCTCA | 10055 |
| rs568514603 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SAE1 | GRCh38.p7 | 19:47208362 | TGTCCCAGGCTCAAG[C/T]GATCCTCCCACCTCA | 10055 |
| rs568610746 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47136765 | AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACAG | 10055 |
| rs568612577 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47178138 | CCCAGCTACTCGGGA[C/G]GGGGAGGCAGGAGAA | 10055 |
| rs568651011 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47178721 | CAAGTGATCCATGCA[C/T]CTCGGCCTTCCAGGT | 10055 |
| rs568691444 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47193993 | GAAGCAGGGTGTGTC[-/T]TTTTTTTTTTACCTG | 10055 |
| rs568709290 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47192425 | AGCTAATTTTTGTAT[G/T]TTTAATAGAGATGGG | 10055 |
| rs568846280 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182304 | GTATGACATTCCCCA[A/G]TGGGTTTTTGGTGTC | 10055 |
| rs568921160 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | SAE1 | GRCh38.p7 | 19:47160297 | TGCGATCTCGGCTCA[C/G]TGCAACCTCCGCCTC | 10055 |
| rs568932525 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47156270 | AGCAAGATCCTGTCT[-/A]AAAAAAAAAAAAGCA | 10055 |
| rs568944718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47194261 | TTAGAGAATGGCCCT[C/T]AACACAGGCTGCTCA | 10055 |
| rs568946698 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47132393 | AGCTGGGACTACAGG[C/T]GTGCCCCACCACATC | 10055 |
| rs568957462 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47132970 | AGGGTTGTTTTGATA[C/G]GTTGGCCAGGGAAGG | 10055 |
| rs568981611 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47131770 | CAGTGGCGCGATCTC[C/G]GCTCACTGCAACCTC | 10055 |
| rs569028764 | snp | A/G | 0.000329772 | 0.0128366 | synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47152900 | TTTCTTTCTGCAGGT[A/G]TGTCTGACTTGCTGC | 10055 |
| rs569098708 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47133318 | AGTGAATCCGCCTCC[C/T]AGGTTCAAGCGATTC | 10055 |
| rs569162134 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | SAE1 | GRCh38.p7 | 19:47168409 | CCTGTGCTAAAACAG[G/T]TCTCTTGCCTCAGCC | 10055 |
| rs569164588 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47159638 | CTGCTCACTGCAGCC[G/T]CCCAAGTAGCTGGAA | 10055 |
| rs569205701 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47169257 | TTAGTTTTGTTTTGG[-/T]TTTTTTTGAGGAGTC | 10055 |
| rs569217236 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47133848 | CTCTTTTAGGTTTCA[G/T]ATTTGTTTTTTTTGT | 10055 |
| rs569248129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47180648 | GGCAACAAAACGAGA[C/T]CCCATCTCTACAAAA | 10055 |
| rs569269500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47146147 | TAAAAGTAGTTTGGT[A/G]TTTTTAGAGTGTGAG | 10055 |
| rs569280048 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47140807 | TTTCAATAAAACAAA[A/G]CGTAAACATGGTATT | 10055 |
| rs569284449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47179904 | GCAATTCTGAAACTA[C/T]TTACTGTTCTTCTAA | 10055 |
| rs569314642 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47146888 | ACATGTAGGGTTTAT[A/G]GATATCTGAGAGAAA | 10055 |
| rs569381888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47194679 | CAAGAATGCCTGCCC[A/G]CCCGCAGGCAGGTTA | 10055 |
| rs569383170 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47200224 | AAGTGTGAGCCACCA[C/T]GCCCAGCCTCTTTTT | 10055 |
| rs569446250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47167588 | GCATCCTTAGCAAGC[C/T]TTGTAAACTGCCTGG | 10055 |
| rs569478310 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210650 | GATCCTGCAGCAGTT[A/G]GTCGGGGAGAAAAGT | 10055 |
| rs569485144 | snp | C/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47182861 | GCCAAAGTGGGAGGA[C/T]TGCTTGAGGCCAATA | 10055 |
| rs569487073 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47175139 | TTTTTTTTGCCTACT[A/G]TAAAGTCAAGCCTCA | 10055 |
| rs569505623 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47148035 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCA | 10055 |
| rs569531351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47174184 | ATCATGTTTACCACT[C/T]TCTCCCAGATGGCAT | 10055 |
| rs569535939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47189094 | GCTCAGTGTATATTT[A/G]TTGAATGAACAATTG | 10055 |
| rs569646417 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47203840 | CTGCCTGCTTTCTCT[C/G]ACCCCATTCATCTTT | 10055 |
| rs569649242 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SAE1 | GRCh38.p7 | 19:47196564 | AGACAGGGTTTCACT[A/G]TGTTGGCCAGGCTGG | 10055 |
| rs569718159 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47204901 | TCTGTACAGGATGAC[C/G]CGTGACCCTGTTAGG | 10055 |
| rs569726800 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47195609 | AGGCTTTAAACTGGT[C/T]CTGCCTAGAATGTGT | 10055 |
| rs569736382 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47186978 | TGGGGCTGTCTGGGT[C/T]GCTTCTGGGTCCCCA | 10055 |
| rs569806957 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47203258 | GCTTCCTACATGTTA[A/G]CACAGGCCTGCTCCC | 10055 |
| rs569852626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47175691 | GCAGTGAGCCGAGAT[C/T]GTGCCACTGCACTCC | 10055 |
| rs569870382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47141564 | GGAAGAGTTCGGGGA[A/G]GGGGAGTGCTTGCTG | 10055 |
| rs569909749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47135310 | ATCCATTAGTCATCC[C/T]TCCTTCCCCTCCACC | 10055 |
| rs569952825 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47148740 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGAATTAC | 10055 |
| rs569991968 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47162924 | CTGAGCCTGGCAAGT[G/T]TAGGCAGCAGTGAGC | 10055 |
| rs570055115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47205635 | AATGTTCTAAGTGGG[A/G]AATGGGAATGTACAT | 10055 |
| rs570136940 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129440 | GCTGAGACTACAGGC[A/G]TGTGCCACCACGCCC | 10055 |
| rs570144459 | snp | A/C | 0.00398564 | 0.0444627 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130424 | AAGCCTTCCCTGACC[A/C]CCCCTGTTACTCTGT | 10055 |
| rs570170201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47135889 | GTTCACTGCAAGCTC[C/T]GCCTCCCAGGTTCAC | 10055 |
| rs570209716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47197819 | CTAACTGCGTAACAC[C/T]GCAGTGTGTGACCTT | 10055 |
| rs570215692 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191556 | TCTGAGGCCTTGCAG[A/C/G]AGTCACGTGGAAACT | 10055 |
| rs570294495 | snp | A/G | 0.00016506 | 0.00908311 | intron-variant, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197373 | CTTCCTGAGGACTTT[A/G]TCAGGTTGGTGTCAG | 10055 |
| rs570308063 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47150453 | ACTTTCAAATCCCAA[A/G]GCAATCTGAGAGCAT | 10055 |
| rs570345966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47149788 | ACAGGAACAGTAATA[C/T]ATTTTAGGGCTGTGC | 10055 |
| rs570347848 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47156493 | CAAAAAAAAAAGTTT[G/T]CTTTGCCTGTTTTTT | 10055 |
| rs570383951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47155980 | TCTTGACCTCGTGGT[C/T]CACCTGCCTCAGCCC | 10055 |
| rs570397069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47137619 | TCTCCCGCCTCAGCC[C/T]CCAAGTAGCTGGGAC | 10055 |
| rs570441223 | in-del | -/A | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176823 | TCGCCATCTGTGAGC[-/A]AAAGGTCTCTTCTTT | 10055 |
| rs570469283 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176665 | GATGTTTTTTATTGC[C/G]CCATTCACAATTCAG | 10055 |
| rs570500194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47191867 | GAGACCATCCTGGCT[A/G]ACACGGTGAAACCCC | 10055 |
| rs570530223 | in-del | -/GTTTT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184838 | GTTTTGTTTTGTTTT[-/GTTTT]TGAGACAGTCTCACT | 10055 |
| rs570533637 | snp | C/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SAE1 | GRCh38.p7 | 19:47143509 | GCTGCGGGCCTCTCG[C/G]GTGCTTCTTGTCGGC | 10055 |
| rs570596674 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47151881 | TGGGGCCATGTTGAC[C/G]GCCTTGCAGGCCGTG | 10055 |
| rs570628248 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47206721 | TGTGTACTGTTGGAC[C/G]CTTCCACCTGGCTAG | 10055 |
| rs570692900 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47168536 | TGGACTCAGGTGATC[A/G]TGCCACTTTGGCCTG | 10055 |
| rs570701546 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47165106 | TTTTTTTTTTTGAGA[C/G]GGAGTCTTGCTCTCT | 10055 |
| rs570717477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47178824 | CAAATTACATTTGTG[C/T]ACTGAAGCAGGGAGG | 10055 |
| rs570759278 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47171933 | ATTTATGCATTTATT[A/T]TTTTGAGACGGAGTC | 10055 |
| rs570807685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47186070 | CATGGTGAAACCCCG[C/T]CTCTACTAAAAATAC | 10055 |
| rs570817593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47145390 | GACCTCAGGTGATCC[A/G]CTGGCCTCGGCCTCC | 10055 |
| rs570870717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47144779 | TGCTTTGTATAGTGC[C/T]TGAACCTAACAAGTA | 10055 |
| rs570916873 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47201644 | TGGGAGGAGTTTTTT[A/T]AATTATTATTATTGG | 10055 |
| rs570931519 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47208975 | CCATGGACACACAGC[G/T]TGTAAGGGACAGAGC | 10055 |
| rs570943017 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47133034 | TATGGGAAAGAGCCC[C/T]GTGGTCATCTGGGAG | 10055 |
| rs570988641 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47132429 | ACTAATTTTTGTTTT[G/T]TTTTTTTTTTGTAGG | 10055 |
| rs571005559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47136261 | CTCCTGCCTAAGCCT[C/T]CCAAGTAGCTGAGAT | 10055 |
| rs571025390 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47139137 | TTGTATTTTGAGTAG[A/G]GATGGAGTTTCACCA | 10055 |
| rs571041880 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47172999 | AGTGCCCACTGGAAG[C/G]CAGGTCTGTTTTGAT | 10055 |
| rs571126170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47209102 | TTTAGAATTTTTTTT[C/T]CCCTCTATTCCTCTT | 10055 |
| rs571129121 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47138356 | GCCAGAAGTTACCTT[C/G]TTTGTGCCTGTTTTC | 10055 |
| rs571226127 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209858 | GTGTGCTGTTCTTGA[A/G]TTTTCGTTTAGGATT | 10055 |
| rs571250874 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47202448 | TCACCCCACCACACC[A/G]AGCTAATTTTTGTAT | 10055 |
| rs571298872 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47188204 | AAATAAAAAATGAAC[C/T]ACCAGGCATGGTGGT | 10055 |
| rs571318276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47185930 | ATGTTTTGAGTGCCG[A/G]CATAACACTCAAAAA | 10055 |
| rs571336322 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47188164 | GACCAGCCTGGGCAA[A/C]ATGGTGAGACCTCGT | 10055 |
| rs571343712 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47152742 | TGCAACTTTTCTTTT[G/T]TCTTCTAGCCATAGG | 10055 |
| rs571378811 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47171765 | CACTGCACCTGGCTG[C/T]GCTAATTTTTGTATT | 10055 |
| rs571381720 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47198809 | AGCCATGATTGTCCT[C/G]GTACAGTGGCTCACA | 10055 |
| rs571512746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47147094 | GACAGCCACACCTAA[A/G]AGGGCCCAAATTGAG | 10055 |
| rs571537667 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47160342 | TTCTCCTGCGTTAGC[C/T]TTCCGAGTAGCTGGA | 10055 |
| rs571548984 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47153894 | CCTCCTGGGTTCAAG[C/G]CATTCTCCTGCCTCA | 10055 |
| rs571579984 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47196333 | AGCCACCGCGCCTGG[C/G]TTTTTTTTTTTTTTT | 10055 |
| rs571589014 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47153101 | TATACTTTTTTTTTT[A/T]AAATTATGTATTTAT | 10055 |
| rs571617273 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47133998 | CTCCCGAGTAGCTGG[G/T]ATTACAGGCGCCCGC | 10055 |
| rs571624037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47181230 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG | 10055 |
| rs571673318 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47176074 | GTATCTTGTTGAACA[A/G]TGGTTAACAATTATA | 10055 |
| rs571681256 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SAE1 | GRCh38.p7 | 19:47141395 | GATCCACCCATCTCA[A/G]CCTCCCAAAGTGCTG | 10055 |
| rs571695127 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47180738 | TGAGATGGGAGGATC[A/G]GTTGAGCGCAGGAGG | 10055 |
| rs571756395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47188799 | CAGTTGGAAAGCTGT[C/T]CAGGCCAGGGACAGG | 10055 |
| rs571784476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47141655 | TTGAAGGGGAAAGGC[A/G]TAGGTAGGCATTGAG | 10055 |
| rs571844330 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47161061 | GGCTGGAGTGCAGTG[G/T]CACAAACACAGCTCA | 10055 |
| rs571912519 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47169239 | GAATACAGCCAGAGG[G/T]TTTTTAGTTTTGTTT | 10055 |
| rs571969269 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47168757 | TACAGGTGCCTGCCA[A/C]CACGTCCAACTAATT | 10055 |
| rs572001679 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SAE1 | GRCh38.p7 | 19:47180964 | TGTAACCCTGGGTTG[A/G]ATCTGAGAATAGAGG | 10055 |
| rs572021980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47134258 | GTGTGAGTACAGAGT[A/G]TAGAATTAATGGAGG | 10055 |
| rs572025651 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47181690 | CGCCATGTTAGCCAG[G/T]CTGGTCTCGAACTCC | 10055 |
| rs572036236 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47206280 | GCACTTTACCTTTTG[C/T]CCCATGTCACCCCAT | 10055 |
| rs572045865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47134785 | CAGTGAAGAATGGAT[A/G]GGGGCCTCTGAGTGG | 10055 |
| rs572047635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47168474 | GCACCCAGCTAACTT[A/G]TAGAGATTGGGGTCT | 10055 |
| rs572049859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47175235 | TAGGCACTACTCTTG[C/T]TTCCATGTTCCTGGC | 10055 |
| rs572059034 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47141163 | CCTGCCACCACGCCT[C/G]GCTAATTTTTGTATT | 10055 |
| rs572060483 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47189135 | AGGCCCAGGGCTTTG[C/G]CTTAGGAAACAGGCT | 10055 |
| rs572079885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47197540 | CTAGAATAGCAATAT[A/G]TAAAAAATAAAGAGG | 10055 |
| rs572136320 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190501 | GCTGCTAACTGGAGT[C/G]TGACCTTCGAGAAAG | 10055 |
| rs572150123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47161539 | AAAAAAGACACCTGG[A/G]AGGGGCAGATACAGC | 10055 |
| rs572172104 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47162488 | TTTGGTAACTTCAGG[C/T]GTTTTTTTTCCATTC | 10055 |
| rs572231608 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47202646 | GGGCTGGGCGCAGTG[A/G]CTCACACCTGTAATC | 10055 |
| rs572241165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47196958 | GAGGCCGAGGCGGGC[A/G]GATCACGAGGTCAGG | 10055 |
| rs572275095 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47211041 | GCCCCAGGCAAGAAA[C/T]GTCTAGTTTCTACAA | 10055 |
| rs572380647 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137520 | AAATTTTTTTTTCTC[C/G]CTCTGTTACCCAGGC | 10055 |
| rs572432397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47142794 | TTGATTTTTGCTCAT[A/G]TGGCATCTCCTCAGA | 10055 |
| rs572482929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47205003 | TTTGAGGGTCTTCTG[A/G]AACATTTGGGTTGCT | 10055 |
| rs572527859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176705 | GTCCGCATGCATGTG[C/T]TTGCCATGTTTAGAT | 10055 |
| rs572558630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47149263 | GCAACCTCCGCCTCC[C/T]CTGTTGAAGTGATTC | 10055 |
| rs572568744 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47184371 | TAAAATGGGGGTGGT[A/T]ACAGTTGTACCTACC | 10055 |
| rs572569379 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SAE1 | GRCh38.p7 | 19:47181427 | GATAATTGTCTCATG[A/G]TTATTTAAGAGAATG | 10055 |
| rs572585018 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SAE1 | GRCh38.p7 | 19:47207467 | TGCCTAGGTGATGTC[C/T]TCCTCTTTAAATGGT | 10055 |
| rs572618820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47176039 | CTAAATTTCTAGGAG[A/G]ACTACTGTTAAGTTT | 10055 |
| rs572654087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47183518 | CAGGCACCTCGTGAC[A/G]TTTTCTTATTCCACT | 10055 |
| rs572657441 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47169959 | TTACCCCGGGAGAGC[G/T]TTTGGCTCTGATTTC | 10055 |
| rs572674786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47136202 | AGAGGACAGTGGCAC[A/G]ATCTCAGCCCAGTAC | 10055 |
| rs572686464 | snp | A/G | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190953 | CACTTGGAATCCTAG[A/G]TGCTGTGTCCCTGTA | 10055 |
| rs572718851 | in-del | -/CT | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47137521 | AATTTTTTTTTCTCG[-/CT]CTGTTACCCAGGCTG | 10055 |
| rs572761831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47157119 | AACTCTCAGACTCTC[C/T]AGCAAGGCGGCGTTG | 10055 |
| rs572801421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47143250 | AGCTGAGATTACAGG[C/T]GCCTGCCACTACGCC | 10055 |
| rs572852068 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130606 | TTGCTGGGATCTCAG[C/T]ATGCACTCCTTAAAT | 10055 |
| rs572877512 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47172116 | TAGAAACGGGGTTTC[A/C]CCATGTTGGCCAGGC | 10055 |
| rs572984618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47185544 | CTCCTGACCTCAAGT[A/G]ATCCTCCCACCTCTG | 10055 |
| rs572987410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47138530 | ATGTACCAGATTTCT[A/G]TAATTCTGCTGATGG | 10055 |
| rs573015209 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47144915 | CCGCACACTGCAACC[G/T]CCGCTTCCCGGGCTC | 10055 |
| rs573025505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47138066 | TTATTTTTTTGAGAC[A/G]GAATTTCTCTCTTGT | 10055 |
| rs573042874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47151255 | CCTGGGTTCAAGTGA[C/T]TCTCCTGCCTCAGCC | 10055 |
| rs573064006 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47192579 | AGACAGCCTCTCTCT[C/G]TAGCCCAGACTGGAG | 10055 |
| rs573079879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47157730 | CTGAGCTGGAAGGTA[C/T]CAAAATATTCCCCAG | 10055 |
| rs573100916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47192223 | GTAATTATTATCACC[C/T]TTCCTACTGGTTTGT | 10055 |
| rs573107456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47166345 | AGTGTGAAAATTTCA[A/G]ATTTGATCCAGGCCT | 10055 |
| rs573170159 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SAE1 | GRCh38.p7 | 19:47178306 | AACCGTTGAAAAATG[C/T]GGAGTGCCTGCTTGT | 10055 |
| rs573173420 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47198267 | GGTGCCTGCCACCAC[A/G]CCCAGCTAATTTTTT | 10055 |
| rs573209174 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47186218 | GCATTCCAGCCTGGG[A/C]AACAGAGAGAGACTC | 10055 |
| rs573210372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47198920 | GGTGAAACCCTGTCT[C/T]TACAAAAAATAGAAA | 10055 |
| rs573240158 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | SAE1 | GRCh38.p7 | 19:47177529 | ATGTCCAGCTATTTT[A/T]AAAAATCTGTTTGTA | 10055 |
| rs573274998 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47131255 | GATGGGAGCTCTGAA[A/G]GGGGCGTTGGGGAGT | 10055 |
| rs573289007 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47187436 | TTGTAACACTTGATA[A/G]GAAACAGAACCATCC | 10055 |
| rs573320937 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47159179 | TAGGTGACTAATTTG[C/G]AGTACTATTAATACT | 10055 |
| rs573327710 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47194437 | TATAATTTGCTGAAT[A/G]AGTCTACTTTTTCAA | 10055 |
| rs573334320 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47132265 | ACTGTGCCCAGCTTG[-/T]TTTTTTTTTTTTTCT | 10055 |
| rs573364457 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47193630 | AACTTGAGACCAGGA[A/T]TTTTTCTATTTTTAG | 10055 |
| rs573507320 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47207912 | AAGTGCTGGGATTAC[A/G]GATGTGAGACATTAA | 10055 |
| rs573553552 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SAE1 | GRCh38.p7 | 19:47143041 | AATTGTTTTGTGCAG[C/T]ATGGATTAGAGCCTG | 10055 |
| rs573566814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47194461 | TTTTCAATCAACATA[C/T]ACGGAAGAGATATCA | 10055 |
| rs573579036 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163715 | CTGGGCGACAGAGCA[A/C]GACTCTATCTCAAAA | 10055 |
| rs573591632 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47176015 | AAACCCTTCCCATTT[G/T]TTTGTCTTCTAAATT | 10055 |
| rs573631688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47146713 | CAGTAGTTAGTGGTA[C/T]GGCCGGGACCCAGGC | 10055 |
| rs573632947 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47141481 | AGAGCAGTCTGTAGA[A/G]CTATGTAGGAATGTA | 10055 |
| rs573639829 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47139688 | ACACCTTCCGGGTTC[A/C]CACCATTCTCCTGTC | 10055 |
| rs573665297 | snp | G/T | | | intron-variant, missense | SAE1 | GRCh38.p7 | 19:47190054 | TCTCTTTTCCAAAGT[G/T]TGCCTTTTCCATTAC | 10055 |
| rs573667351 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47153935 | TAGCTGAGATTACAG[G/T]CATGCGTCACCATGC | 10055 |
| rs573681346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47152602 | ATGAGAACTATGAAA[C/T]GTGTATATGTTCGTG | 10055 |
| rs573746230 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47138506 | AATGTTGGCCATTAT[C/T]ATTTTATTATGTACC | 10055 |
| rs573755909 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47173703 | AAAATGTTTCCAGAC[A/T]CCACTGCCACATGTC | 10055 |
| rs573768587 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47173154 | CAGGCACGCACCACC[A/G]CACCCAGCTAATTTT | 10055 |
| rs573771485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47145619 | AAAGACTTACTCTGT[C/T]GCCCAGGCTGGAGTA | 10055 |
| rs573787677 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47183958 | TGGTTGGCAAAGCAA[C/T]GCATTAGGGGCCCAT | 10055 |
| rs573807228 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47180087 | GTTTCTTATACGTAG[A/C]TGTAGTAATAGATGT | 10055 |
| rs573838225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47133169 | GCTTTTATTCTAAGT[A/G]TGTGGGAAAACCTGT | 10055 |
| rs573855042 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47141692 | AAATGGTGCATTTTG[C/T]GAGGGTGGAATGTTG | 10055 |
| rs573930374 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47134051 | TATTTTTAGTAGAGA[C/T]GGAGTTTCACCGTGT | 10055 |
| rs573978276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47203486 | GGTCTTTTCCAACCA[C/T]TTATGAATCCCTTGC | 10055 |
| rs573987735 | snp | A/G | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176810 | TTGAGAGTTGGCCTC[A/G]CCATCTGTGAGCAAA | 10055 |
| rs574087734 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47160596 | GAGATGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 10055 |
| rs574180897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47135544 | CAGGGTCTCTCTGTC[A/G]CGCAGACTAGAGTGC | 10055 |
| rs574187256 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47198405 | GCATGAGCCACCACG[C/T]GCTCCATCCACATCT | 10055 |
| rs574200830 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47202126 | AATACATATGAAAAA[C/T]TAGCATTGCTATATT | 10055 |
| rs574214411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47142463 | TTTTGCTTGTGTGTT[A/G]TACTTAACTAGTGCC | 10055 |
| rs574228004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47167845 | AGACGGGATCTAACA[A/G]TGTTCCCCCAGCTTG | 10055 |
| rs574237097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47196029 | GTGTGCCATCACACT[C/T]TGCCTCTTCCGGGTC | 10055 |
| rs574272627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190228 | TTTGATACGATTTGA[C/T]GAGTCATCTTTTGGT | 10055 |
| rs574281113 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | SAE1 | GRCh38.p7 | 19:47147762 | CCAGCCTCAACTGTA[A/T]TTTTTTTTTTTTTTG | 10055 |
| rs574297409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47163543 | GACCAGCCTGGCCAA[C/T]ATGGTGAAACCCCAT | 10055 |
| rs574297541 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47155689 | TCAGGTGATCCACCC[A/G]CCTCAGCCTCCCAAA | 10055 |
| rs574304687 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SAE1 | GRCh38.p7 | 19:47154941 | CCTGAGTGCCCAACA[C/G]TGTACCAGACTCATC | 10055 |
| rs574389009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47175292 | TCTTGTGACAATCTT[C/T]GAAGTATAGTTGTTA | 10055 |
| rs574423532 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47128850 | CTGAGACGGAGTCTT[C/G]CTCTGTTGCCCAGGC | 10055 |
| rs574433117 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47162575 | TAAAGCTTTTTAAAG[A/T]TTCTTGGTCCCTCTA | 10055 |
| rs574480263 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47184644 | TTGAACTCCTGACCT[C/T]AGGTGATCCACCCAC | 10055 |
| rs574494470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47174776 | GACGGGGTTTCACCA[C/T]GTTAGCCAGGATGGT | 10055 |
| rs574515098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47183642 | ACATCTCCCCCACTC[C/T]CCCACCCACTTGGCA | 10055 |
| rs574517054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191704 | GACCAACAAGAGGAG[A/G]TGATTTTTTTTTTCA | 10055 |
| rs574553864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47191209 | TAAGGTCAGAAGTTC[A/G]AGACCAGCCTGGCCA | 10055 |
| rs574623554 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47156835 | TAGAAAGGAGTGGAG[A/G]AGGGATCAGAAGACG | 10055 |
| rs574669784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47204348 | GACTACAGGCGCCTG[C/T]CACCACGCCCAGCTA | 10055 |
| rs574698026 | snp | C/T | 3.3134e-05 | 0.00407012 | intron-variant | SAE1 | GRCh38.p7 | 19:47143642 | CCTCCCCTGCTCTGG[C/T]TCCCCTTTCCAGCAT | 10055 |
| rs574789305 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47201104 | TAGAGTGCAATGGCC[C/T]GATCTTGGCTCACTG | 10055 |
| rs574843578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47185384 | GTGTCGGCTCACTGC[A/G]ACCTCCACCTCCCAG | 10055 |
| rs574868840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47143304 | GAGACGGGGTTTCAC[C/T]GTGTTGGTCAGGCTG | 10055 |
| rs574907677 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47149989 | CTGAGGCAGGAGGAG[A/G]ATCATTTGAACCCAG | 10055 |
| rs574986976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47170616 | GGCTTAAGTGCTCCC[C/T]ATGCCTCAGGCTCCT | 10055 |
| rs575039145 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47133575 | GTTAAAGTGGTCAGA[A/C]ATGGAAGTAAAGATT | 10055 |
| rs575104688 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47173113 | GGCTCACTGCAACTT[A/C]TGCCTCCTGGGTTCG | 10055 |
| rs575134043 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47199880 | AGCCGCTGACCTCAC[A/G]GTGCTGATGTTACAA | 10055 |
| rs575134499 | snp | A/T | 0.00119856 | 0.0244508 | intron-variant | SAE1 | GRCh38.p7 | 19:47151463 | GCCTGTTTTTTACAC[A/T]TTTCTTTCTTTCTTT | 10055 |
| rs575142795 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47199021 | TGAGCCCAGGAAAGC[A/C]GAGGTTGCAGTGAAC | 10055 |
| rs575170268 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130698 | CGCGCCATTTTTGGG[G/T]CTAGGATTGGTTGGA | 10055 |
| rs575231667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47137056 | TCTCTTCCAAAAGTC[A/G]GTTTCATGGGAAAAA | 10055 |
| rs575279562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47158361 | TAGCCCAGAAATAGG[C/T]GCTCAGTAGTTTGTT | 10055 |
| rs575390414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47153285 | AGTAAAATGATTACA[A/G]AATAGTTGGGCGATT | 10055 |
| rs575406494 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47157808 | TCCAACCCCAAGCCC[G/T]TAAGGTTACGAGGCA | 10055 |
| rs575409420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47192612 | CAGCGGTGTGATTTC[A/G]GCTCACCGCAACCTC | 10055 |
| rs575418342 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47193291 | GTCTTGAACTCCTGA[C/G]CTCAGGTGATCCACC | 10055 |
| rs575442304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47144946 | AAGTGATTCTCCTGC[C/T]TCAGCCTCTGAAGTA | 10055 |
| rs575444056 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47146794 | ATGGAAATAGCAAGG[A/T]TATGAAGATGAGGCT | 10055 |
| rs575445676 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47164894 | CCTGACCTCGTGATC[C/T]GCCTGCCTCAGCCTC | 10055 |
| rs575479094 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47151965 | TTGATCAATTGGTTG[A/C]ATGTTCACCTGTGGA | 10055 |
| rs575494505 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47186667 | ACAACTTTCATCCGG[C/T]GCCTCGGAACCTCTT | 10055 |
| rs575496437 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47178443 | AGGAAAGGGAAGCCC[A/C]TTTCCCAGGTCAAAG | 10055 |
| rs575529384 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47159989 | GTGAGCCACAGCTTC[C/T]AGCCTGATTGTTTCC | 10055 |
| rs575561528 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47172824 | GGATGACAGAGTTCT[C/G]TAGGACTTGCTCTGT | 10055 |
| rs575564418 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47159456 | AGACTCCTAGTCCAG[C/T]GTGTAGCACAGTCAT | 10055 |
| rs575601112 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47206154 | TCCTGCCTGCTGGAG[A/G]CAGCTGGTGCCCAGC | 10055 |
| rs575615314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47180885 | CCTGGCAGGTTGTAC[C/T]TCAGCTGAGTGATGA | 10055 |
| rs575677980 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209605 | TGTGGGAGATGCCTG[C/T]CAGGAATGAGCAAGC | 10055 |
| rs575685367 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47132723 | AAACCCAGTCTCTAC[-/A]AAAAAAATACAAAAA | 10055 |
| rs575689207 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163121 | AGTATTTTTCTATGT[A/G]TATACAACAAAATTG | 10055 |
| rs575781975 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47158559 | GGCATGTGAGGGACA[A/G]GCTTTCCAGGCACCA | 10055 |
| rs575926155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47167259 | ACACCCGGCCTGCGC[C/T]CAGATAATTTTTGTA | 10055 |
| rs575966401 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47190021 | TTTTCTATAAATAAC[A/G]TGAAACCGTGCTTGG | 10055 |
| rs575967077 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47140754 | GAGCCCTGATCTTGC[C/T]ACTGCCCTTCAATCT | 10055 |
| rs576001862 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47208566 | CTGCCTCAGCCTCCC[A/G]AGTAGCATGCCACCA | 10055 |
| rs576027747 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191486 | CCAGAAAGGGTATCA[A/G]CACTGCCTGAGCAGA | 10055 |
| rs576031318 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47141113 | TTTGAGTGATTCTCC[A/T]GCCTCACTGTCCCGA | 10055 |
| rs576036934 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47140634 | TCTACAAAAAAAAAA[A/C]AAAACCCATAAATCA | 10055 |
| rs576047534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47194932 | ATTTTTTTAGTAGAG[A/G]CGGGGTTTCACCATG | 10055 |
| rs576055156 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176664 | AGATGTTTTTTATTG[C/T]CCCATTCACAATTCA | 10055 |
| rs576067576 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137917 | TATTTTTAGTAGAGA[C/T]GGGGTTTTACCATGT | 10055 |
| rs576068378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47147348 | GTAGTTGGGACTACA[A/G]GTGCACGCCACCACA | 10055 |
| rs576120816 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47211000 | TCACCCAGAGGACCC[C/T]TCAGGAATCGAGGGG | 10055 |
| rs576155522 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47168367 | TGGAGTGCAGTGGTA[C/T]GATCTGGCTCACTGC | 10055 |
| rs576160750 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137876 | TCGGATTACAGGCGC[C/G]TGCCACCACACCTGG | 10055 |
| rs576219268 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47173909 | CCTGCCTCAGCCTCC[C/T]GACTAGCTGGGACTA | 10055 |
| rs576318014 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47148480 | TTTGAGAGCAGTATG[A/G]AATCTGTAATCTTAC | 10055 |
| rs576333313 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | SAE1 | GRCh38.p7 | 19:47177554 | TTTGTACAGATTGGG[G/T]CAGGGAGGTCTTGCT | 10055 |
| rs576387440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47134586 | TTGGAGGAAACTTTG[A/G]GGAAGCTTGGTGTGT | 10055 |
| rs576389993 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SAE1 | GRCh38.p7 | 19:47196910 | AAAGGTGGCCAGGTG[C/T]CGTGGCTCACACCTG | 10055 |
| rs576390608 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47196149 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 10055 |
| rs576392745 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47183245 | ACATGCATTGTGATC[A/G]TATTAAATCTTCATG | 10055 |
| rs576495928 | snp | G/T | 0.0463947 | 0.145069 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129743 | CTGGGGCCATCCCTG[G/T]TTTTTTTTTTTTTTC | 10055 |
| rs576513685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47161353 | GCACAAAAGAAGATA[C/T]GCAGCATCAATGCAG | 10055 |
| rs576536586 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129109 | AGGCGTGAGCCACCA[A/C]CTCCGGCCTAAGCAA | 10055 |
| rs576582546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190995 | TTTCTTTTGGATTCC[A/G]TTAGGGTTAAGAAGC | 10055 |
| rs576589507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47150696 | TTGCACATAACTTTA[A/G]TCCATGTTATTGCAA | 10055 |
| rs576601326 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47143108 | AGTTAGAACCAAAAT[G/T]ATTTTTTTTTTTTTG | 10055 |
| rs576606416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47155027 | CCTTAACCACCATCC[C/T]GATCTGTGACCTGGA | 10055 |
| rs576632994 | snp | A/G/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190376 | CTCTTGGGGCGGGGC[A/G/T]GAAAGCAGAACAAAG | 10055 |
| rs576654177 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47142674 | CTGTCATTCCTGTCC[C/G]TAGAACATGCCAAGC | 10055 |
| rs576694474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47175389 | TTTATAGACAGTCAG[A/G]ATTTAGACCATGAGG | 10055 |
| rs576694547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47183372 | GTGTTAGAGTCTAAA[C/T]GAGCCAGAGCTGTCA | 10055 |
| rs576729337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47182508 | GTGTGCGCGCACGCA[C/T]GCGCGCGCGCACACC | 10055 |
| rs576733017 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47170437 | CCAGGCCCTGAAGTT[C/G]TGAGATTATAGGCAT | 10055 |
| rs576780835 | snp | A/G | 3.30535e-05 | 0.00406518 | intron-variant | SAE1 | GRCh38.p7 | 19:47169942 | AGGTCTCAAAGCACA[A/G]CTTACCCCGGGAGAG | 10055 |
| rs576807642 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47198024 | CACTCCATGCTTTCA[C/T]CTTACGTGACTACCT | 10055 |
| rs576809940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47177476 | TTATCCTCTCACCTC[A/G]ACCTGCAAAGTAGCT | 10055 |
| rs576871299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47136163 | TTTTCTTTTGAGACC[A/G]AGCCTCGCTCTGTTG | 10055 |
| rs576961437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191781 | TGGGAATAGGCCGGG[C/T]GCGGTGGCTCACACC | 10055 |
| rs577081378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47198203 | CAACTTCTGCCGCCT[A/G]GGTCCAAGCGATTCT | 10055 |
| rs577165072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47171540 | CACTGCAACCTCCAC[C/T]TCCCAGGTTCAAGCG | 10055 |
| rs577165176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47178170 | CGCTTGAAAACCTGG[A/G]AGGCAGAGGTTGCAG | 10055 |
| rs577187923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47200728 | CTCTTTTTGTAAATA[A/G]AGTTTTATTGGCACA | 10055 |
| rs577222922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47184691 | GCTGGGATTACAGGC[A/G]TGAGCCACCACTGCC | 10055 |
| rs577249819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47144303 | GGCACCACTGCACTC[C/T]AGCCTGGGCAACAGA | 10055 |
| rs577378799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47164975 | TATTTTTAGTAGAGA[C/T]GGAGTTTCACCATAT | 10055 |
| rs577463993 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47167025 | GGTGTGACCTTGGCT[C/G]GCTGCAACCTCCACC | 10055 |
| rs577467234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47201103 | CTAGAGTGCAATGGC[C/T]CGATCTTGGCTCACT | 10055 |
| rs577479624 | in-del | -/CT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47170204 | CACAGATTGAGAAAC[-/CT]CTTTTTTTTTCTTTT | 10055 |
| rs577485300 | snp | A/G | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129706 | ATTTTTAATAGAGAT[A/G]GCGTTTCCCTATATT | 10055 |
| rs577579364 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47162290 | TACAAATTGTGCTGC[A/G]TAAGCATTTTGTTTG | 10055 |
| rs577579549 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47131920 | TGACGAGACTGGTCT[C/G]GATCTCCTTACCTCA | 10055 |
| rs577617276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47131172 | GTCTCTCTCTTGGGG[A/G]GACTGGAGGAGTTGA | 10055 |
| rs577660695 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47140689 | TAGTCCCAGGACTCA[A/G]TAGGCCGAGGTGGCG | 10055 |
| rs577699660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47158449 | GGGCACAAGCCTCAC[A/G]TGGACACTGACATGC | 10055 |
| rs577700053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47208429 | CATACCTGGCTAATT[C/T]ATGTCATTTTTCTTT | 10055 |
| rs577746408 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47179985 | TATTGTCAGAAAAGG[G/T]TGTTCCTATGAATGT | 10055 |
| rs577800991 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47132574 | GAGCTACCATGCCTG[C/G]CCTCATTGATCAATA | 10055 |
| rs577808302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47140291 | TTTTATATTTTTAGT[A/G]GAGATAGGGTTTCAC | 10055 |
| rs577817158 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47186723 | GAGGCACAGCTTCTT[C/T]CCCTCTTCTGAGCTG | 10055 |
| rs577869422 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182515 | CGCACGCACGCGCGC[A/G]CGCACACCACTGCCT | 10055 |
| rs577923539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47160120 | AGAGAACAGAATACC[A/G]AAGAAGACAATAGAC | 10055 |
| rs577999865 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47142338 | GTAGTGAGCTGAGAT[C/T]ACGCCACTGCACTCC | 10055 |
| rs578051121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47167717 | AGGGAGGAAGAAAGA[C/T]ACCTCTGTAAGTTTG | 10055 |
| rs578093032 | in-del | -/TCT | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47134393 | TTCAGATCTGTGGGG[-/TCT]TCTTTGATGGGGTGG | 10055 |
| rs578103928 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47188524 | GTGACACAGGTTACC[A/C]CAGCAAGTGTATCGG | 10055 |
| rs578137296 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47186505 | GTTCATTGAGCATTC[A/G]TGCTCCCCTCTGCTG | 10055 |
| rs578173357 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47173133 | TCCTGGGTTCGAGCG[A/T]TTCTACAGGCACGCA | 10055 |
| rs578193624 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47210004 | GCTTCAGGGCTAGGA[A/G]GGAGGAGCCTGCCCT | 10055 |
| rs578223632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47160544 | GGACTACAGATGCCC[A/G]CCGCCATGCCCGACT | 10055 |
| rs578232049 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SAE1 | GRCh38.p7 | 19:47194946 | GACGGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 10055 |
| rs745307280 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47173670 | CAGTAATATCTCCCC[A/T]CCCAGCTCTAACATC | 10055 |
| rs745379971 | in-del | -/TTTT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184802 | TTTTGTTTTGTTTTT[-/TTTT]GTTTTGTTTTGTTTT | 10055 |
| rs745408219 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47188760 | AATAGGGAGTCTAGA[A/G]CTGTGCTCTTCGCTG | 10055 |
| rs745415804 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47139017 | GAAGCACTAATGCCA[A/G]GGTCCTAAGGTGGGA | 10055 |
| rs745471571 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47149751 | AAAGCCTTAGAAGGA[A/G]GCCTGCATAAGGCAA | 10055 |
| rs745494450 | snp | A/C/G | 3.32913e-05 | 0.0040798 | intron-variant | SAE1 | GRCh38.p7 | 19:47197212 | TGGCTTTATAACCTG[A/C/G]CTTCTTTTTCTTATT | 10055 |
| rs745511032 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47153445 | CATGACAGGACTTGC[C/T]GTGTTTTGACTTTGT | 10055 |
| rs745529511 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47152173 | TCTTTTGACCATGAT[A/C]ACAAAGCTTCTCCCG | 10055 |
| rs745576348 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47205430 | CCGAGGAGATATTTG[A/G]AGGGGGAAGAAAAGT | 10055 |
| rs745586488 | in-del | -/CA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47203048 | TAGGAGCTGGCAGAG[-/CA]CACACTTCCTTTGGG | 10055 |
| rs745634776 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47203227 | ATACTTTAATTTCAC[A/G]CCTCAAATTTCCCTT | 10055 |
| rs745793022 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47166296 | GGGGGCCAGCTTTCC[C/T]GATGTGCCTTAATCT | 10055 |
| rs745818408 | snp | G/T | 1.66158e-05 | 0.0028823 | intron-variant | SAE1 | GRCh38.p7 | 19:47152857 | GGCAGTGATTCACAG[G/T]TTGCAAAACTCAAAC | 10055 |
| rs745819379 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47143932 | TAAAAATGACCTGAG[G/T]GACTAACTGAAAATG | 10055 |
| rs745841350 | snp | C/G | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129707 | TTTTTAATAGAGATA[C/G]CGTTTCCCTATATTG | 10055 |
| rs745875805 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47194593 | CCTGTGTGATGTGGG[A/C]GAAAGAGTATTGTCC | 10055 |
| rs745884077 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47142756 | TGCTGCCAAATATCT[A/G]TGTGTTTGTCCTTTA | 10055 |
| rs745909426 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47158417 | ATTTGAGACGGATTT[C/T]GTCACAATCAGGTCT | 10055 |
| rs745935402 | snp | C/G | 1.64741e-05 | 0.00286998 | intron-variant, synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197327 | GATACGAAATGATGT[C/G]CTTGACTCACTGGGT | 10055 |
| rs745954555 | in-del | -/T | 1.65637e-05 | 0.00287777 | intron-variant | SAE1 | GRCh38.p7 | 19:47153074 | GGGGAGAACATAACA[-/T]TTTCTCCTTTTTATA | 10055 |
| rs746138363 | in-del | -/T | 8.23859e-05 | 0.00641764 | intron-variant | SAE1 | GRCh38.p7 | 19:47203646 | GTTCCCAGTGCTCCA[-/T]TTTCCTTGTCTTCCT | 10055 |
| rs746140574 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47207898 | GCCTCGGCCTCCCTA[A/C]GTGCTGGGATTACAG | 10055 |
| rs746169891 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47185956 | AAAAAAATGCTTATT[C/G]GCCCCGGGCGTGGTG | 10055 |
| rs746205387 | snp | C/T | 1.64806e-05 | 0.00287054 | intron-variant | SAE1 | GRCh38.p7 | 19:47155109 | CTCCCCTTGTCACCC[C/T]CTAGGGAGAAAACTA | 10055 |
| rs746208819 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47196733 | CCCCTTCAAACTCAT[A/G]TATACTTCATTGAAT | 10055 |
| rs746289550 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47194456 | CTACTTTTTCAATCA[A/G]CATATACGGAAGAGA | 10055 |
| rs746289553 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47135013 | TTTGTCCATTTTCAG[A/C]CGAGGTTTTTAGAAA | 10055 |
| rs746328006 | snp | C/T | 2.71205e-05 | 0.00368232 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209366 | AAGTCATTGGCCCGA[C/T]ACAAAACATTTCCTG | 10055 |
| rs746367618 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47149054 | GGGCCTCTCTGTGTT[G/T]TCCAGGCTAGTCTTG | 10055 |
| rs746384131 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47147074 | TTCTGAGATGGAAGC[C/T]TGGGGACAGCCACAC | 10055 |
| rs746405159 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47199099 | GTCTCAATACATATA[A/G]CGTAAGGCTGGGCGC | 10055 |
| rs746480170 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47162187 | TTTTATTTTTGTTTT[G/T]TGCTAGAGTCTTTGT | 10055 |
| rs746486274 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47136496 | TTTTTACCCGAGTCT[-/T]TTTTTTTTTTTTTTT | 10055 |
| rs746494771 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47161512 | AGAGCTGCTGGTACA[-/T]TTGTGTGGATTAAAA | 10055 |
| rs746520342 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47206766 | CAGTATTGGTAAAGG[A/G]CTCCTGGCCCTATTA | 10055 |
| rs746546255 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47202679 | AGCGCTTTGGGAGGC[A/C]GAGGCGGGCGGATCA | 10055 |
| rs746614185 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47179291 | CAGGTGGATTGCCTG[A/G]GCTCAGAAGTTTGAG | 10055 |
| rs746630734 | snp | C/T | 1.7067e-05 | 0.00292117 | intron-variant | SAE1 | GRCh38.p7 | 19:47150197 | AATATGTGTATTATT[C/T]CTAGGTAACTCCAGA | 10055 |
| rs746651039 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47175865 | AGATAGTTTTAGACA[C/G]AAAGATTATCTGAAT | 10055 |
| rs746652536 | snp | G/T | 4.94907e-05 | 0.00497422 | intron-variant | SAE1 | GRCh38.p7 | 19:47143616 | AACAGGTGCGCTGTT[G/T]TGAGCTCATTCCTCC | 10055 |
| rs746659079 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47140937 | CATTGAAACCTCTGC[C/T]TCTCAGGTTCAAGCG | 10055 |
| rs746744054 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47153736 | TTCCAGACATCTCCT[A/G]ACTCTAGTGTTTTAT | 10055 |
| rs746744555 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47206431 | GAGCGCCTATGGAAA[A/G]CTTACACTAGGAGAT | 10055 |
| rs746789894 | in-del | -/A | 1.69095e-05 | 0.00290765 | intron-variant | SAE1 | GRCh38.p7 | 19:47150411 | TCTGCTGTGGGAATT[-/A]AACAAATTAAGGTGC | 10055 |
| rs746795886 | snp | A/C | 0.000100481 | 0.00708733 | intron-variant | SAE1 | GRCh38.p7 | 19:47197216 | TTTATAACCTGCCTT[A/C]TTTTTCTTATTCCCA | 10055 |
| rs746836608 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47205671 | TGTAGCCTAAAATGA[C/T]GACACCACCAATAAT | 10055 |
| rs746899632 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47168377 | TGGTACGATCTGGCT[C/T]ACTGCAGCCTCGACC | 10055 |
| rs746931519 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47152618 | GTGTATATGTTCGTG[C/G]ATTACAGAAAACATT | 10055 |
| rs746972922 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant, missense, intron-variant | SAE1 | GRCh38.p7 | 19:47130868 | GCGGCGGTAGGTGGC[C/G]CGCGGGTCCGGCGGG | 10055 |
| rs747006336 | in-del | -/TT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47138078 | GACGGAATTTCTCTC[-/TT]GTTGCCCAGGCTGGA | 10055 |
| rs747014121 | snp | A/G | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129406 | TTCAAGCGATTCTCC[A/G]GCCTCAGCCTCCCAA | 10055 |
| rs747015192 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182543 | CCTTATCAGTGGTAG[A/G]GAATGCAGACCACAG | 10055 |
| rs747025709 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167598 | CAAGCTTTGTAAACT[A/G]CCTGGTAACTGATAG | 10055 |
| rs747028560 | snp | G/T | 1.64855e-05 | 0.00287097 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150342 | TGAGGATATAGAGAA[G/T]AAACCAGAGTCATTT | 10055 |
| rs747041045 | snp | A/C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47144856 | GTGTTTTTGCGAGAC[A/C/G]AGTCTTGCTGTGATG | 10055 |
| rs747086515 | snp | A/G | 1.64738e-05 | 0.00286995 | intron-variant, missense, synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47203731 | GATTTTGGCACAGGA[A/G]ATTGTGAAGGTAAAA | 10055 |
| rs747111727 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB, synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47130852 | TCCGGGCGTGCTGCC[G/T]GCGGCGGTAGGTGGC | 10055 |
| rs747115514 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47194899 | AGGCGTGCGCCACCA[C/T]GCCTGGCTAATTTAT | 10055 |
| rs747127843 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47165694 | AAGACAGGTACCACC[G/T]TTTGCATCTGCTGCT | 10055 |
| rs747171378 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47144008 | TGATTCTCATTTAGG[G/T]CTGAGGCGAGCTCAG | 10055 |
| rs747221490 | in-del | -/TTTTT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184839 | TTTTGTTTTGTTTTG[-/TTTTT]GAGACAGTCTCACTC | 10055 |
| rs747238786 | snp | C/T | | | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47211118 | GAAAAAAAGGCCAGG[C/T]GTGGTGGCTCACGCC | 10055 |
| rs747248960 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47133149 | ACCAAATGATTTGAG[G/T]AGTAGCTTTTATTCT | 10055 |
| rs747294644 | snp | A/G | 0.000108044 | 0.00734917 | missense, nc-transcript-variant, intron-variant | SAE1 | GRCh38.p7 | 19:47130947 | TGGTGGAGAAGGAGG[A/G]GGCTGGCGGCGGCAT | 10055 |
| rs747360315 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47192398 | GGATTAAAAGCGTCC[A/G]CCACCATGCCCAGCT | 10055 |
| rs747367118 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47169846 | GCCCTGTTAAAGAAG[C/T]CCTGGAGGTGGACTG | 10055 |
| rs747384716 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47145406 | CTGGCCTCGGCCTCC[C/G]AAAGTGCGGTGATTA | 10055 |
| rs747391466 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47210007 | TCAGGGCTAGGAGGG[A/T]GGAGCCTGCCCTTTT | 10055 |
| rs747424932 | snp | A/G | 1.65097e-05 | 0.00287308 | intron-variant | SAE1 | GRCh38.p7 | 19:47155234 | TGTAACGTGGGGGCA[A/G]AGGTCAGAAACCCTG | 10055 |
| rs747496742 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47171419 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGAAATACA | 10055 |
| rs747530752 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47135191 | CAATCCAATTATATT[A/C]TTTTAGTTGCTTTGA | 10055 |
| rs747554818 | snp | C/G | 3.29457e-05 | 0.00405854 | synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47155159 | AGGAGTAGAAGATGG[C/G]CCCGACACCAAGAGA | 10055 |
| rs747555824 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47201018 | ATACGCCACCATGCC[C/T]AGCTATTTTTTTTTA | 10055 |
| rs747574256 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47165982 | TGATTGGCCTGGTTG[C/G]GGTCCTGTGCCCACT | 10055 |
| rs747589375 | in-del | -/TT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47153984 | TTAGTAGAGACAGGG[-/TT]TTTCCATGTTGGTCA | 10055 |
| rs747648014 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47200283 | CTGTTGCCTAGGCTA[C/G]AGTGCAGTGGCACAT | 10055 |
| rs747654993 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47149422 | GTGATCCTCCTGCCT[C/T]GGCCTCCCAAAGTGC | 10055 |
| rs747735791 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47202071 | TGGACACAGCTCTTG[A/G]GATTGGAATGGATAC | 10055 |
| rs747764040 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47173342 | CTGCCTGCCACAGAA[A/G]TCATATAGCTACTGT | 10055 |
| rs747841235 | snp | C/G | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47176428 | CTCACAAAGAAACCT[C/G]ATTTTGTTTCACTAT | 10055 |
| rs747844227 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47142203 | AGCCTGAACAACATG[G/T]TGAAACTCCGTCTGT | 10055 |
| rs747849490 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47141088 | CTTACTGCAACCTCC[A/G]CCTCCCAGGTTTGAG | 10055 |
| rs747874730 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47177325 | CTATAACAGAGGGCT[A/G]TAGAAACTATCATGT | 10055 |
| rs747893176 | snp | C/G | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191553 | CAGTCTGAGGCCTTG[C/G]AGCAGTCACGTGGAA | 10055 |
| rs747917411 | snp | C/T | 3.36118e-05 | 0.00409936 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150203 | TGTATTATTCCTAGG[C/T]AACTCCAGAAGATCC | 10055 |
| rs747923160 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47207491 | AAATGGTAGCTTGTG[A/G]TGAAATTTCAATCCT | 10055 |
| rs747926192 | in-del | -/ACTTA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47135455 | TGCCTGATTTATTTC[-/ACTTA]ACTTAACATAATAAC | 10055 |
| rs747942003 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184369 | ACTAAAATGGGGGTG[A/G]TAACAGTTGTACCTA | 10055 |
| rs747987384 | snp | A/C | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190378 | CTTGGGGCGGGGCGG[A/C]AAGCAGAACAAAGGA | 10055 |
| rs748049994 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47155040 | CCCGATCTGTGACCT[C/G]GAGAGGCTTTTTTTG | 10055 |
| rs748067590 | snp | A/G | 1.64735e-05 | 0.00286993 | intron-variant, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197317 | TGTTGCTCCAGATAC[A/G]AAATGATGTGCTTGA | 10055 |
| rs748141889 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47153851 | GGCTGGAGTGCAATG[A/G]CACCATCTCAGTTCA | 10055 |
| rs748155879 | in-del | -/TTT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47195737 | TTCCTTTTTTTCTTC[-/TTT]TTTTTTTTTTTTTTT | 10055 |
| rs748160422 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47168824 | GGTCAGGCTGGTCTT[A/G]AACTCCTGACCTCAG | 10055 |
| rs748163901 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47206572 | GTTTTCCTTTCTCTC[C/T]ATCCCCACCGTCCAC | 10055 |
| rs748190342 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184401 | CTCATTCTGTCTTTT[G/T]TGTTTTTTGCTTGTT | 10055 |
| rs748192937 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47153007 | GCTACCATGGATACA[C/T]ATTTGCCAATCTAGG | 10055 |
| rs748197478 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182678 | GAGAGAACAGAACTG[A/G]TTAGTCACCGACTCT | 10055 |
| rs748266843 | snp | A/G | 1.64735e-05 | 0.00286993 | stop-gained, utr-variant-3-prime, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209207 | TTCTTCTTCTTCGAT[A/G]GCATGAAGGGGAATG | 10055 |
| rs748271001 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47164760 | TTCAAGCGATTCTCC[C/T]GCCTCAGCCTCCTGA | 10055 |
| rs748289334 | in-del | -/T/TT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47160214 | GTTCAAAATCCTGCA[-/T/TT]TTTTTTTTTTTTTTT | 10055 |
| rs748308984 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47192310 | GGCTAGATTGCAGTG[A/G]CACGATACCGGCTCA | 10055 |
| rs748357203 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47197388 | GTCAGGTTGGTGTCA[A/G]TATTTATCACTGTTT | 10055 |
| rs748374056 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47146303 | GACAGGAAGGGTGAC[A/G]TGGTTAGCTTTGGGC | 10055 |
| rs748377759 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47131147 | GGCGGGAATTCTGTG[C/T]TCTGGGATCGTCTCT | 10055 |
| rs748396300 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47144925 | CAACCTCCGCTTCCC[A/G]GGCTCAAGTGATTCT | 10055 |
| rs748405281 | snp | A/G | 6.59076e-05 | 0.00574016 | intron-variant | SAE1 | GRCh38.p7 | 19:47203748 | TTGTGAAGGTAAAAC[A/G]TCACTGTGGAGCAGA | 10055 |
| rs748470739 | in-del | -/TA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47148093 | TCCATGTCCTCGTTT[-/TA]TATGGGATTCCCACA | 10055 |
| rs748485588 | in-del | -/C | 3.30442e-05 | 0.0040646 | intron-variant | SAE1 | GRCh38.p7 | 19:47209153 | TCTTTTCATTTTTCT[-/C]CCCAGGCCCTGTCTC | 10055 |
| rs748531562 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47194944 | GAGACGGGGTTTCAC[A/C]ATGTTGGCCAGGCTG | 10055 |
| rs748537482 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47177702 | CATTTGCATTATTCC[A/T]TAATAATCAAAGTAA | 10055 |
| rs748567448 | snp | A/G | 0.000107799 | 0.00734085 | synonymous-codon, nc-transcript-variant, intron-variant | SAE1 | GRCh38.p7 | 19:47130972 | CGGCATTAGCGAGGA[A/G]GAGGCGGCACAGTAT | 10055 |
| rs748570539 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47178242 | CAAGACTCCATCTCC[-/A]AAAAAAAAAAAAGAA | 10055 |
| rs748612356 | snp | C/T | 3.29468e-05 | 0.00405861 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47169855 | AAGAAGCCCTGGAGG[C/T]GGACTGGAGCAGTGA | 10055 |
| rs748670603 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47173572 | CACTACTGACATTCT[A/G]TGCTGGATAACACTG | 10055 |
| rs748694489 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47151794 | TTATGCCAGGTGTCC[C/T]TTGAACTTGTAGAGT | 10055 |
| rs748734839 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47187256 | CCCAGCTATGTCACT[C/T]CTCTGAGCTTCACAC | 10055 |
| rs748740027 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47144922 | CTGCAACCTCCGCTT[C/T]CCGGGCTCAAGTGAT | 10055 |
| rs748759632 | snp | G/T | | | synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150243 | GTTCTTGATTCGTAC[G/T]GGGTCTGTTGGCCGA | 10055 |
| rs748761418 | snp | A/G | 0.000119253 | 0.00772091 | intron-variant, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47131035 | CCAGAAACGGTCAGG[A/G]CCGGCGCGGCTTGAG | 10055 |
| rs748767550 | snp | C/G | 1.65839e-05 | 0.00287953 | intron-variant | SAE1 | GRCh38.p7 | 19:47169953 | CACAACTTACCCCGG[C/G]AGAGCTTTTGGCTCT | 10055 |
| rs748791708 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47154293 | ACGGGGTTTCACTAT[C/G]TTGGCTATGCTGGTC | 10055 |
| rs748824322 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47203019 | TTGGTGAGCACACAG[A/C]ATTGTGTTCAGGAGT | 10055 |
| rs748915320 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167463 | GCCAGGATGGTCTCG[A/C]TCTCCTGACCTTGTG | 10055 |
| rs748942504 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47151118 | TATGTTACATGAGAG[A/G]TTAGAATTTGGGTTG | 10055 |
| rs748988073 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47201105 | AGAGTGCAATGGCCC[A/G]ATCTTGGCTCACTGC | 10055 |
| rs749011340 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47166112 | GGACTTTTTGTGGGC[C/T]GCTTCCCTGTTCTGC | 10055 |
| rs749027748 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47164127 | TTTCACTCAATAAGC[A/G]TTCCCCAAATCTGCT | 10055 |
| rs749059372 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47180755 | TTGAGCGCAGGAGGT[C/T]GAAGCTGCAGTGAGT | 10055 |
| rs749096718 | snp | C/T | | | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47211052 | GAAATGTCTAGTTTC[C/T]ACAAATTTCATAAAC | 10055 |
| rs749211023 | snp | A/T | 3.29696e-05 | 0.00406001 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150338 | ACACTGAGGATATAG[A/T]GAAGAAACCAGAGTC | 10055 |
| rs749218146 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47142315 | CTTGGACCTGGGAGG[C/T]GGAGGTTGTAGTGAG | 10055 |
| rs749233726 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47185080 | CCGCCTCGGCCTTCC[-/A]AGTACTGGGATTATA | 10055 |
| rs749234377 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47157369 | TGTTAACAAACGGAG[A/G]AGTACAAAAGCTGCT | 10055 |
| rs749296363 | in-del | -/TATT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47202288 | AAAATTATACCTATT[-/TATT]TATTTATTTATTTAT | 10055 |
| rs749303525 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47198121 | CTCTCTCTCTTTTTT[A/T]TTTTTGAGACAGAGT | 10055 |
| rs749307971 | in-del | -/C | 1.64806e-05 | 0.00287054 | intron-variant | SAE1 | GRCh38.p7 | 19:47203774 | GCAGAAAATTGTTAA[-/C]CATGACTTTGTATAT | 10055 |
| rs749332124 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47206778 | AGGACTCCTGGCCCT[A/G]TTATTATTAATAGCA | 10055 |
| rs749344641 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47171157 | TTTTTATATTTTTAG[A/T]AGAGACAGGGTTTCA | 10055 |
| rs749368470 | in-del | -/C | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190473 | ATGGCTTTCTTCCTG[-/C]CCCCCCTCCACTGCT | 10055 |
| rs749372799 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47140688 | ATAGTCCCAGGACTC[A/G]ATAGGCCGAGGTGGC | 10055 |
| rs749455509 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47134598 | TTGAGGAAGCTTGGT[A/G]TGTTCTGAGATCCTA | 10055 |
| rs749456238 | in-del | -/AT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47192178 | CATGGCTTAGCACTC[-/AT]GTGATCTTCACGATA | 10055 |
| rs749478662 | in-del | -/ATATT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47158911 | CTAGGGTAACGTGAC[-/ATATT]AGGAGGATGGTGGGA | 10055 |
| rs749523768 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47133240 | GTTTGTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 10055 |
| rs749537833 | snp | C/T | 2.46904e-05 | 0.00351349 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209358 | GAAAACTGAAGTCAT[C/T]GGCCCGATACAAAAC | 10055 |
| rs749543582 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184559 | GGGATGACAGGCACC[C/T]GCCACCATGCCCATT | 10055 |
| rs749665937 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47200088 | GGCGCCCGCCACCAC[G/T]CCCAGCTAATTTTTT | 10055 |
| rs749667929 | snp | G/T | 1.6473e-05 | 0.00286988 | stop-gained, utr-variant-3-prime, synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209218 | CGATGGCATGAAGGG[G/T]AATGGGATTGTGGAG | 10055 |
| rs749690817 | in-del | -/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47204500 | CTGTACCCAGCCGCA[-/C]CCCCCCCCCTTTTTT | 10055 |
| rs749717662 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47169391 | TCTGGGACTACAGGC[A/G]GCCGCCAGCATGCCT | 10055 |
| rs749727248 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47145049 | CTCTTGTTGCCCAGG[C/T]TGGAGTGCAATGGCG | 10055 |
| rs749759411 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47162061 | GTGGCCAGTAAGCAC[A/T]TGTGGCCATTGGCAT | 10055 |
| rs749838919 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47189812 | AAGTACTGGTTTATT[C/T]GGTGGCCTTGGTGAT | 10055 |
| rs749843235 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47173786 | CTTTTCTTTCTTTTC[-/T]TTTTTTTTTTTTTTT | 10055 |
| rs749849943 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47175723 | GCCTGGGCAACAGAA[C/T]GAGACTCTGTCTCAA | 10055 |
| rs749858950 | in-del | -/T | 0.00130527 | 0.0255133 | intron-variant | SAE1 | GRCh38.p7 | 19:47153090 | TTCTCCTTTTTATAC[-/T]TTTTTTTTTTTAAAT | 10055 |
| rs749867613 | snp | A/G | 9.88419e-05 | 0.00702931 | intron-variant, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197284 | CCAGTTCTGATACAT[A/G]TGAGGAAGATTCTGA | 10055 |
| rs749882630 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47207282 | TTCCCTGGAAAAATG[G/T]CTGACTAACACTATT | 10055 |
| rs749896549 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47135541 | AGACAGGGTCTCTCT[G/T]TCGCGCAGACTAGAG | 10055 |
| rs749926903 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47206380 | GCCTGCAGTCCAAGG[A/G]CCTCAGACTCACCTT | 10055 |
| rs749978793 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47132076 | CAAGACTTCCTCTCA[C/T]CTCAGTCTTCTGAGT | 10055 |
| rs749987829 | snp | C/T | | | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210653 | CCTGCAGCAGTTAGT[C/T]GGGGAGAAAAGTGGT | 10055 |
| rs750022540 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47133634 | GAGATAAAAATATTG[G/T]TGGCTTGAAACTCAA | 10055 |
| rs750057733 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47183780 | GTGCCATCTTCCCTC[A/G]GCAAGAGGGGTTGGC | 10055 |
| rs750194718 | snp | A/G | 3.37866e-05 | 0.00411001 | intron-variant | SAE1 | GRCh38.p7 | 19:47153087 | CATTTTCTCCTTTTT[A/G]TACTTTTTTTTTTTA | 10055 |
| rs750237753 | in-del | -/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47164378 | TCACCGTGTTAGCTA[-/G]GGATGGTCTCCATCT | 10055 |
| rs750266783 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47193398 | CTGCCAAGTGTTGAG[A/G]TAGCATTGAGGGTTG | 10055 |
| rs750319183 | snp | A/T | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47152978 | CATCAAGTTCTTTAC[A/T]GGAGATGTTTTTGGC | 10055 |
| rs750321051 | snp | A/C | 1.79812e-05 | 0.00299838 | missense, utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209311 | ACCTGTATTCCCTGT[A/C]CCCTTCCTTCATGAA | 10055 |
| rs750326692 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47144771 | GGGCAGACTGCTTTG[C/T]ATAGTGCTTGAACCT | 10055 |
| rs750339417 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47196458 | AACTTCCGCCTGCTG[C/G]ATTCAAGTGATTCTC | 10055 |
| rs750343046 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47159314 | CCCGTCATTAAAGAA[A/G]CAGTCGAGTTCTTTT | 10055 |
| rs750373171 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47161371 | AGCATCAATGCAGAT[A/G]ATGGAACAAAACAAA | 10055 |
| rs750399649 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47175296 | GTGACAATCTTTGAA[A/G]TATAGTTGTTATCCC | 10055 |
| rs750445762 | snp | C/T | | | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47211009 | GGACCCCTCAGGAAT[C/T]GAGGGGAAAGCTGCC | 10055 |
| rs750481241 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47173348 | GCCACAGAAGTCATA[G/T]AGCTACTGTTTCTTC | 10055 |
| rs750494056 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47201116 | GCCCGATCTTGGCTC[A/C]CTGCAACCTCCGCCT | 10055 |
| rs750507984 | snp | G/T | 3.29576e-05 | 0.00405928 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47169911 | ACGACCTCCGACTAC[G/T]TTCTCCTTCAAGGTG | 10055 |
| rs750510316 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47138582 | TCTATTAATTCACAG[C/T]CATTTGAGTAACAGT | 10055 |
| rs750632593 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47169825 | TTCCACAGAAGGTGG[C/T]CTTCTGCCCTGTTAA | 10055 |
| rs750644499 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47187710 | TGTTTTTAGCAGAGA[C/T]GGGGTTTCACCATGT | 10055 |
| rs750649320 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47151554 | TTGGCTCACTGCAAC[C/T]TCCGCCTCCCTGGTT | 10055 |
| rs750688968 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47202251 | ATAGAACAGAAGAGT[A/T]ATAGTTGATAATATT | 10055 |
| rs750732624 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47186946 | AGACTGTGAGCTCCG[C/T]GTGTGAGGGCAAGGC | 10055 |
| rs750739165 | snp | C/T | 1.65894e-05 | 0.00288 | synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150369 | ATTTTTCACTCAATT[C/T]GATGCTGTAAGTTTC | 10055 |
| rs750862955 | snp | A/G | | | intron-variant, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47180206 | CCAGAAGCACTGAAC[A/G]CACTCATGCCAAGAT | 10055 |
| rs750874542 | snp | G/T | 1.64849e-05 | 0.00287092 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150247 | TTGATTCGTACTGGG[G/T]CTGTTGGCCGAAATA | 10055 |
| rs750898820 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47165753 | TTTTGTTTTTAATTG[C/T]TATGAGTTAGTTTGA | 10055 |
| rs750949309 | snp | C/T | 5.49858e-05 | 0.00524308 | intron-variant | SAE1 | GRCh38.p7 | 19:47150184 | CAAGACTTAAAAAAA[C/T]ATGTGTATTATTCCT | 10055 |
| rs751008114 | snp | A/G | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150281 | CTGAAGCCTCTTTGG[A/G]GCGAGCTCAGAATCT | 10055 |
| rs751063357 | snp | G/T | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129191 | ATCCGTGCACTTTGG[G/T]AGGCCGAGGCGGGTG | 10055 |
| rs751088718 | snp | C/G/T | 3.29474e-05 | 0.00405867 | intron-variant, missense, synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47203680 | TTTTAGGTACTGCTT[C/G/T]TCCGAGATGGCCCCA | 10055 |
| rs751133872 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47208587 | CATGCCACCATACTC[A/G]GCTAATTTCTGTATT | 10055 |
| rs751151565 | snp | C/T | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191435 | TGTTAAACGCTAGTC[C/T]TGTCAGTCACTCCTG | 10055 |
| rs751168373 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47141868 | TTACATGATGCAGCC[C/G]AAGATCTTGATGAGT | 10055 |
| rs751210868 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47131971 | CTCCTGAAGTGCTGG[A/G]ATTACAGGAGTGAGC | 10055 |
| rs751228288 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47170864 | GCTTATGAAAGGTGG[A/G]GTTGTTTTTCCTCTT | 10055 |
| rs751238955 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47154951 | CAACAGTGTACCAGA[C/G]TCATCATGTTATCAA | 10055 |
| rs751326109 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47207413 | TCATGAATGATGGGA[C/T]GGTGCTCCTGGGAAC | 10055 |
| rs751407529 | in-del | -/TTG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47149021 | ATGAGGTTGCAATTT[-/TTG]TTGTTTTTTGAGAGA | 10055 |
| rs751407578 | in-del | -/A | 5.02938e-05 | 0.00501442 | intron-variant | SAE1 | GRCh38.p7 | 19:47197416 | TTAGTCTGGACAGAT[-/A]AAAGTTTGTTTTCAG | 10055 |
| rs751410899 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47134261 | TGAGTACAGAGTATA[C/G]AATTAATGGAGGGGT | 10055 |
| rs751475706 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184101 | GTCAAGCTCTGGAAT[C/T]GCCTGACATTTTTAA | 10055 |
| rs751530429 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47148337 | AGTAAGATAGAGAGT[A/G]TGCTGTGGATGGTTG | 10055 |
| rs751550530 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163080 | TGTTAATCCTACTAC[A/C]AAATGATAACTATAA | 10055 |
| rs751562535 | in-del | -/GT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182464 | AAAGAAAAAAGCGTA[-/GT]GTGTGTGTGTGTGTG | 10055 |
| rs751590115 | in-del | -/AACC | 1.66225e-05 | 0.00288287 | intron-variant | SAE1 | GRCh38.p7 | 19:47209133 | AAAGCACTTGAGCTA[-/AACC]CTCTTTTCATTTTTC | 10055 |
| rs751590559 | in-del | -/TG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47194105 | TGTAGCTTCTAAAAC[-/TG]TGTCCTCCTCAGTTG | 10055 |
| rs751735984 | snp | C/G | 0.000203273 | 0.0100794 | intron-variant | SAE1 | GRCh38.p7 | 19:47180345 | AGAAAGTAAGGAAGT[C/G]CTCTAAGAATGATAG | 10055 |
| rs751754287 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47193846 | AAAAAAAAAAGAAAG[-/A]AAAGAAAAAGAAAAA | 10055 |
| rs751777120 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47175433 | TGGACTTAGTTTTCA[A/G]CATATTTAAGATATA | 10055 |
| rs751802321 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47188214 | TGAACCACCAGGCAT[A/G]GTGGTGCATGCCTGT | 10055 |
| rs751862977 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47189605 | AGCCAACCCTGGGGA[G/T]GAGTCTACGTTCAGC | 10055 |
| rs751878501 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182499 | TGTGTGTGTGTGTGC[A/G]CGCACGCACGCGCGC | 10055 |
| rs751923755 | in-del | -/TT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47200409 | GCCTAATTTTTTTTT[-/TT]TTTTTTTTTTTTTGT | 10055 |
| rs752009125 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167913 | ACTGCTTTTTTCTGG[C/T]TAGGCACAGTGGCTC | 10055 |
| rs752122280 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167367 | GCCTCAGCCTCCCGA[A/G]TAGCTGGGACTGCAG | 10055 |
| rs752128094 | snp | C/T | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130105 | TACAGGTGCGAGTCA[C/T]CGTGCCTGGCCTATT | 10055 |
| rs752156012 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47153721 | GGAAGGACAGTCATG[A/T]TCCAGACATCTCCTA | 10055 |
| rs752171166 | snp | A/C | 1.66854e-05 | 0.00288833 | intron-variant | SAE1 | GRCh38.p7 | 19:47150384 | CGATGCTGTAAGTTT[A/C]TTATTATAAAATCTG | 10055 |
| rs752194153 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47161216 | ATCTCTTGCTGTGTT[G/T]CCCAGGCTGATCTCA | 10055 |
| rs752211028 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47180593 | CCAAGAGGCTGAGGC[A/G]AATTGATCACTTGCA | 10055 |
| rs752231090 | in-del | -/TC/TCTC | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129823 | CTTTCTTTCTTTCTT[-/TC/TCTC]TTTTTTTTTTTTTTA | 10055 |
| rs752255716 | in-del | -/TG | 1.6681e-05 | 0.00288794 | intron-variant | SAE1 | GRCh38.p7 | 19:47197210 | AGTGGCTTTATAACC[-/TG]CCTTCTTTTTCTTAT | 10055 |
| rs752276810 | snp | C/G | 6.58946e-05 | 0.0057396 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SAE1 | GRCh38.p7 | 19:47143584 | AGGAGTGAAAGGACT[C/G]ACCATGCTGGATCAC | 10055 |
| rs752280199 | snp | A/G | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47152937 | GATGTCATAGTTAAA[A/G]TTGACCAGATCTGTC | 10055 |
| rs752291501 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47144417 | AAAAAACACTGGATC[A/G]GGCCAGGCACAGTGG | 10055 |
| rs752295795 | snp | C/G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47202596 | CGCCCTAATTATACC[C/G/T]GTTTAGATTGTGCAC | 10055 |
| rs752333709 | snp | A/C | 5.04155e-05 | 0.00502048 | intron-variant | SAE1 | GRCh38.p7 | 19:47150400 | TTATTATAAAATCTG[A/C]TGTGGGAATTAAACA | 10055 |
| rs752358511 | snp | A/G | | | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210789 | GTGCAAGTCAGTGGC[A/G]TCAGGGTCAGCAGTT | 10055 |
| rs752407502 | snp | A/G | 1.67652e-05 | 0.00289522 | intron-variant | SAE1 | GRCh38.p7 | 19:47197417 | TTAGTCTGGACAGAT[A/G]AAGTTTGTTTTCAGG | 10055 |
| rs752435535 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47172295 | ATGAGTGTTGCATGT[A/G]AGTGGGCTGCACTCA | 10055 |
| rs752436321 | in-del | -/GTTG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137727 | TGTGTGTGTGTGTGT[-/GTTG]TTTTTTTTTTTTTTT | 10055 |
| rs752464253 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47192568 | TTTATTTTTTGAGAC[A/G]GCCTCTCTCTGTAGC | 10055 |
| rs752475414 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47208767 | TCACCATGTTGCACA[G/T]ACTGGTCTTGAATTC | 10055 |
| rs752517981 | snp | A/G | 0.000128526 | 0.0080154 | utr-variant-5-prime, nc-transcript-variant, missense, intron-variant | SAE1 | GRCh38.p7 | 19:47130881 | GCGCGCGGGTCCGGC[A/G]GGCGGTTGGCTTGAG | 10055 |
| rs752571713 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47136537 | TTTCGCTCTTGTTAC[C/T]CAGACTGGAGTATGG | 10055 |
| rs752623673 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47135827 | GAAACGGAGTCTCGC[C/T]GTGTCGCCTAGGCTG | 10055 |
| rs752630517 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47185592 | ATTACAGGCTGAGCT[A/G]CTGCGCCCAGCCTAT | 10055 |
| rs752645046 | snp | C/T | 1.64787e-05 | 0.00287038 | intron-variant | SAE1 | GRCh38.p7 | 19:47169804 | TCCTAAGCAGTTCTG[C/T]CTTTTTTCCACAGAA | 10055 |
| rs752653336 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47186653 | CCTTTTCCCCATCAA[C/G]AACTTTCATCCGGCG | 10055 |
| rs752711989 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47134431 | TGTCATCATGAGGCA[C/T]TAACATTGGTGGGAG | 10055 |
| rs752732125 | in-del | -/AGGTTAACA | 6.59903e-05 | 0.00574376 | intron-variant | SAE1 | GRCh38.p7 | 19:47143470 | CTGTTCTGTATCATC[-/AGGTTAACA]ATGTTTGTCTTACAG | 10055 |
| rs752755131 | in-del | -/AC | | | intron-variant | SAE1 | GRCh38.p7 | 19:47148636 | TTTTTTTTTTTTGAG[-/AC]AGAGTCTCACTCTGT | 10055 |
| rs752788279 | snp | C/T | 2.06922e-05 | 0.00321647 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209334 | TTCATGAAGGCATCT[C/T]CAGGCAAGGAAAACT | 10055 |
| rs752841383 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47198428 | CCACATCTCCTTCCA[A/G]GCAGCTCTGGGATCA | 10055 |
| rs752871377 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47148533 | TTATCCTGTCTTTGA[A/G]GCTCTGCTCTGCTGA | 10055 |
| rs752879707 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47161803 | CTTATGTATGTATTT[A/C]CAAGCAACACATAGA | 10055 |
| rs752908098 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47177362 | CCTGGTTTTTGTTTG[-/T]TTTTTTTCCCCCCCA | 10055 |
| rs752909042 | snp | A/T | 8.55341e-05 | 0.00653909 | intron-variant | SAE1 | GRCh38.p7 | 19:47150166 | TTATTTTCCCTAAAA[A/T]TACAAGACTTAAAAA | 10055 |
| rs752956240 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163392 | AACAACTGTTTACAT[A/G]GCAATTCCATTAGGT | 10055 |
| rs752974154 | snp | C/G | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176801 | TCCACTGTCTTGAGA[C/G]TTGGCCTCGCCATCT | 10055 |
| rs753013659 | in-del | -/TT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47145938 | TCCCATTCTCAAGGT[-/TT]TTTTTTTTTTTTTTT | 10055 |
| rs753022159 | snp | C/T | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47191136 | GATGGGTAGGTTGGG[C/T]GTAGTGGGTCATGCC | 10055 |
| rs753040349 | snp | A/G | 1.68729e-05 | 0.00290451 | intron-variant | SAE1 | GRCh38.p7 | 19:47197189 | CCATCTCCAAAAAAA[A/G]AAAAAAGTGGCTTTA | 10055 |
| rs753077577 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47208945 | GGTAATGTTTGGAGA[A/G]GTTAAATAATCTCCC | 10055 |
| rs753108441 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47179253 | GCTCACGCCTGTAAT[C/T]CTAGCACTTTGGGAG | 10055 |
| rs753177150 | snp | A/G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47189646 | CAGGGAATTGGGGCC[A/G/T]AGGTGTCTGGCACAG | 10055 |
| rs753242960 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47154742 | CTCAGGTGACACGCC[C/T]GCCTTGGCCTCCCAC | 10055 |
| rs753267215 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47206317 | CTCTCATCCCCAGTA[C/T]TCCTTCATACTTATT | 10055 |
| rs753283640 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47205227 | AGCTTGGGAGGACAG[G/T]TTGGAGGCCAGCCCT | 10055 |
| rs753290677 | in-del | -/GA | 0.000118842 | 0.0077076 | utr-variant-5-prime, nc-transcript-variant, frameshift-variant, intron-variant | SAE1 | GRCh38.p7 | 19:47130909 | AGCGGGACCGGAGCT[-/GA]GAGGCAGGAAGAGCC | 10055 |
| rs753308561 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182086 | CCACTGCACCCAGCC[C/T]GTTAGATAATTTAGA | 10055 |
| rs753346970 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47168100 | GGGGGCGCTGAGGCA[C/T]GAGAATTGCTTGAAC | 10055 |
| rs753364342 | snp | A/T | 1.66183e-05 | 0.00288251 | intron-variant | SAE1 | GRCh38.p7 | 19:47153074 | GGGGAGAACATAACA[A/T]TTTCTCCTTTTTATA | 10055 |
| rs753429118 | snp | C/T | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130666 | ACCACGTGGGCAACG[C/T]CCTCGGGGCCTTAAG | 10055 |
| rs753512655 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182330 | GTGTCCAGTAATGAC[A/T]AAAACTGCTGAGAAA | 10055 |
| rs753545684 | snp | A/T | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191557 | CTGAGGCCTTGCAGC[A/T]GTCACGTGGAAACTG | 10055 |
| rs753605012 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47194458 | ACTTTTTCAATCAAC[A/C]TATACGGAAGAGATA | 10055 |
| rs753678559 | snp | C/T | 1.64732e-05 | 0.0028699 | intron-variant, synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47203720 | GTGGTTGGAGGGATT[C/T]TGGCACAGGAAATTG | 10055 |
| rs753682041 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47143824 | ACTCACACCCCCTCA[C/T]TGAGCTTGCCTGCCT | 10055 |
| rs753711292 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47158359 | CCTAGCCCAGAAATA[A/G]GTGCTCAGTAGTTTG | 10055 |
| rs753716181 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47159043 | TGTTAGGTGCTGCCA[A/G]AGATGATGAGATGCC | 10055 |
| rs753737999 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137186 | CTGAGGTCAGGAGTT[C/T]GAGACTAGCCTGGCC | 10055 |
| rs753776646 | in-del | -/AT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47168283 | CCAGCATGATGCCAC[-/AT]GTGTCATTTCCAAAT | 10055 |
| rs753807476 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47173248 | GTGAACCGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 10055 |
| rs753902023 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47151381 | GTCTTGAACCCCTGA[C/T]CTCAGGTAATCCACC | 10055 |
| rs753932878 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47186711 | GATGCAAATAGCGAG[G/T]CACAGCTTCTTTCCC | 10055 |
| rs753934270 | snp | C/T | 1.64819e-05 | 0.00287066 | intron-variant | SAE1 | GRCh38.p7 | 19:47155221 | TCAAAAAGGTATGTG[C/T]AACGTGGGGGCAGAG | 10055 |
| rs753989192 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47135930 | TGCCTCAGCCTCCCT[A/T]GTAGCTGGGACTACA | 10055 |
| rs754007109 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47148865 | GTGATCTGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 10055 |
| rs754061427 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47165386 | TGAGCCACCGCACCC[A/G]GCCTTGTTATTAGTC | 10055 |
| rs754093688 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47201783 | GCATTACAGCTGCCC[A/G]CCACCACACCCGGCT | 10055 |
| rs754131483 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47147852 | CAAGCTCTGCCTCCC[A/G]GGTTCACACCATTCT | 10055 |
| rs754145503 | in-del | -/GTTTT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47144999 | ACCACGCCTGGCTAA[-/GTTTT]GTTTTGTTTTTTTTT | 10055 |
| rs754151472 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163477 | TCACGCCTGAAATCC[C/G]AGCACTTTGGGAGGC | 10055 |
| rs754153502 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47178498 | TTTTATTTTTGAGAC[A/G]GAGTCTAGCTTTGTT | 10055 |
| rs754224748 | snp | G/T | 0.000237093 | 0.0108853 | intron-variant | SAE1 | GRCh38.p7 | 19:47150176 | TAAAAATACAAGACT[G/T]AAAAAAATATGTGTA | 10055 |
| rs754227143 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47201839 | GGTTTCACTATGTAG[G/T]TCAAGCTGGTCTTGA | 10055 |
| rs754278107 | snp | C/T | 1.64789e-05 | 0.0028704 | synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47143599 | GACCATGCTGGATCA[C/T]GAACAGGTGCGCTGT | 10055 |
| rs754278164 | snp | A/G | 3.29522e-05 | 0.00405894 | intron-variant, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197271 | AAAGGAAGAGATCCC[A/G]GTTCTGATACATATG | 10055 |
| rs754314641 | snp | C/T | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176853 | TTTATTATTCTCCCA[C/T]GGCATGTTGCAAAAC | 10055 |
| rs754321335 | snp | A/G | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47176352 | ACTAATGTGACTGAC[A/G]ATGCCTTAGGAATTC | 10055 |
| rs754338600 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47205072 | TGCAGACTTTGCTAT[C/T]TGCCCGAAGATGTTA | 10055 |
| rs754387606 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47141739 | AATTTTTAATTAAAT[G/T]AATAGCAAACTCTTA | 10055 |
| rs754402185 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47156457 | GCACTCCAGCCTGGC[G/T]ACAGAACGAGACTCT | 10055 |
| rs754424591 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47140805 | TGTTTCAATAAAACA[A/G]AACGTAAACATGGTA | 10055 |
| rs754427683 | snp | A/G | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47191272 | AAAAGTTATTTGGGC[A/G]TGGTTGTGGGCGTCT | 10055 |
| rs754472831 | in-del | -/GGCGGC | 0.000108208 | 0.00735473 | cds-indel, nc-transcript-variant, intron-variant | SAE1 | GRCh38.p7 | 19:47130952 | GAGAAGGAGGAGGCT[-/GGCGGC]GGCATTAGCGAGGAG | 10055 |
| rs754523702 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47154531 | ACAGACTTTCACTCA[A/G]TTGCCCAGGCTGGAG | 10055 |
| rs754526712 | snp | A/T | 1.6703e-05 | 0.00288985 | intron-variant | SAE1 | GRCh38.p7 | 19:47150387 | TGCTGTAAGTTTCTT[A/T]TTATAAAATCTGCTG | 10055 |
| rs754529519 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47177152 | GACCATCTTTGAGCC[A/C]CAGAATTGAAGCTGA | 10055 |
| rs754539420 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47142012 | CTGCTTCCTACTGAC[C/T]TCAGAGAAGTCTTGG | 10055 |
| rs754571820 | snp | A/G | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150284 | AAGCCTCTTTGGAGC[A/G]AGCTCAGAATCTCAA | 10055 |
| rs754633314 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47208624 | AGAGACAGGTTTCAC[C/T]GTGTTGGCCAGGCTG | 10055 |
| rs754654639 | in-del | -/TATT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47153110 | TTTTTTTAAATTATG[-/TATT]TATTTATGTGTAGAG | 10055 |
| rs754673099 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47159392 | CTTGTCTCTGTCTCC[C/G]CGCTTCCATTTTAAG | 10055 |
| rs754698356 | snp | G/T | 1.66076e-05 | 0.00288158 | intron-variant | SAE1 | GRCh38.p7 | 19:47197408 | TATCACTGTTTAGTC[G/T]GGACAGATAAAGTTT | 10055 |
| rs754703173 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47157246 | GAACCATAATTATCC[A/G]GAGTGAACCTTGGTG | 10055 |
| rs754710401 | in-del | -/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47147379 | CCTGGCTAATTTTTT[-/G]TATTTTTTGTAGAGA | 10055 |
| rs754716355 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47154958 | GTACCAGACTCATCA[G/T]GTTATCAATGGCAGA | 10055 |
| rs754749524 | snp | A/G | 1.64732e-05 | 0.0028699 | intron-variant, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197311 | CTGAGTTGTTGCTCC[A/G]GATACGAAATGATGT | 10055 |
| rs754756844 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47170987 | TGGCACTTTTTTGTT[G/T]GTTTTTGAGATGGAG | 10055 |
| rs754802717 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47136143 | ATGGGATTTATTGCA[A/G]TTTTTTTTCTTTTGA | 10055 |
| rs754878820 | in-del | -/TTG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47192234 | ACCCTTCCTACTGGT[-/TTG]TTGTTGTTGTTGTTG | 10055 |
| rs754978254 | snp | C/T | 3.29516e-05 | 0.00405891 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47155206 | CTGAGACAACGATGG[C/T]CAAAAAGGTATGTGT | 10055 |
| rs754984525 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon, utr-variant-3-prime, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209205 | ACTTCTTCTTCTTCG[A/G]TGGCATGAAGGGGAA | 10055 |
| rs755010598 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47132811 | GAGCATCACCTGAGC[C/T]CCTGGGAGGTGGAGG | 10055 |
| rs755019241 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182633 | GGTGACCCACAAATG[C/T]GGCTCAGTGCCTTAC | 10055 |
| rs755034763 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47148451 | AATTAGATGTTTGAT[A/G]TGTGAAGAAATACTT | 10055 |
| rs755051336 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47145823 | TGCACCCATCTTAGA[C/G]CGTATTATGTAGTTT | 10055 |
| rs755053858 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47198374 | ACCTTGGCCTCCCAA[A/T]GTGCTGAGATTACAG | 10055 |
| rs755070990 | in-del | -/GG/GTGA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182482 | TGTGTGTGTGTGTGT[-/GG/GTGA]GTGTGTGTGTGTGTG | 10055 |
| rs755134365 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47193416 | GCATTGAGGGTTGCA[A/G]AAGCTGTGTTCTTGA | 10055 |
| rs755207850 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47175539 | GTCAGGAGTTCGAGG[A/G]CAGCCTGGCCAAGAT | 10055 |
| rs755262334 | snp | A/G | 4.94637e-05 | 0.00497287 | intron-variant | SAE1 | GRCh38.p7 | 19:47143479 | ATCATCAGGTTAACA[A/G]TGTTTGTCTTACAGG | 10055 |
| rs755360517 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137604 | CCGGGTTCAAGGGAT[C/T]CTCCCGCCTCAGCCC | 10055 |
| rs755361348 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47169847 | CCCTGTTAAAGAAGC[C/T]CTGGAGGTGGACTGG | 10055 |
| rs755382652 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47188259 | GGGAGGCTGAGGCAG[A/G]AGGATCACTTGAGTT | 10055 |
| rs755398035 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47187032 | TGGAGGGGGGGTGCT[C/T]AGGAAGTGATTTTTG | 10055 |
| rs755438329 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47205062 | GTACATTCTTTGCAG[A/G]CTTTGCTATTTGCCC | 10055 |
| rs755448030 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47145939 | CCCATTCTCAAGGTT[-/T]TTTTTTTTTTTTTTT | 10055 |
| rs755481715 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47151673 | ATCTGTGCATTTGTC[C/T]TGTTTTCTTTTTCCT | 10055 |
| rs755496478 | in-del | -/AAG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47193839 | TCAAAAAAAAAAAAA[-/AAG]AAAGAAAAGAAAAAG | 10055 |
| rs755537700 | snp | C/T | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130229 | GGGCACAAAGTGCAA[C/T]ACATAGTAGGGACAT | 10055 |
| rs755546627 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47205078 | CTTTGCTATTTGCCC[A/G]AAGATGTTAAATTTG | 10055 |
| rs755618877 | in-del | -/TTTTTTTTT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47201367 | TCTGGTTCCTTTTTT[-/TTTTTTTTT]TTTTTTTTTTTTTTG | 10055 |
| rs755686598 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47180653 | CAAAACGAGACCCCA[A/T]CTCTACAAAAAATAA | 10055 |
| rs755732583 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47154164 | GGCACGATCTTGGCT[C/T]ACTGCAACCTCCACC | 10055 |
| rs755769106 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47186190 | GCTTGCGGTGAGCCG[A/T]GATCCCGCCACTGCA | 10055 |
| rs755776739 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47194408 | TATGTAGGAACCCTT[G/T]TCCTGGTAGAGAGTA | 10055 |
| rs755805051 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47142260 | GTGACAGTAGGCGCC[C/T]GTAATCCCAGCTACT | 10055 |
| rs755811018 | snp | A/C | 3.29462e-05 | 0.00405857 | intron-variant, synonymous-codon, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47203693 | TTCTCCGAGATGGCC[A/C]CAGTGTGTGCGGTGG | 10055 |
| rs755844129 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47158276 | CCTGTGGTTTTCACA[C/T]CCTCTAGGAAGCTGG | 10055 |
| rs755865053 | snp | A/G | 1.68091e-05 | 0.00289901 | intron-variant | SAE1 | GRCh38.p7 | 19:47150402 | ATTATAAAATCTGCT[A/G]TGGGAATTAAACAAA | 10055 |
| rs755888800 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47172341 | TGATAGTGGGATCAG[A/G]TGTGGAAGAGGCACC | 10055 |
| rs755918257 | snp | A/C | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150325 | GATGTGAAGGTGGAC[A/C]CTGAGGATATAGAGA | 10055 |
| rs755919822 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47208795 | TTCCTGGGCTCAAGT[G/T]ATTCTCCCACCTCAG | 10055 |
| rs755937161 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47157329 | TATCTGAATAGCTCC[A/G]TGAATTTGGTGGGGG | 10055 |
| rs755976843 | in-del | -/TTTC | | | intron-variant | SAE1 | GRCh38.p7 | 19:47151464 | CCTGTTTTTTACACT[-/TTTC]TTTCTTTCTTTCTTT | 10055 |
| rs756003193 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47195424 | TTGGGGTCTTCTTAC[A/C]CAGTAGTTCTGACTC | 10055 |
| rs756007057 | snp | C/T | 1.79107e-05 | 0.0029925 | intron-variant | SAE1 | GRCh38.p7 | 19:47197421 | TCTGGACAGATAAAG[C/T]TTGTTTTCAGGATTT | 10055 |
| rs756009171 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47207564 | ACCCTTTCTCAGAAA[C/G]ATGTATGTGCATACA | 10055 |
| rs756081635 | snp | C/T | 0.000126255 | 0.00794427 | utr-variant-5-prime, nc-transcript-variant, missense, intron-variant | SAE1 | GRCh38.p7 | 19:47130893 | GGCGGGCGGTTGGCT[C/T]GAGCGGGACCGGAGC | 10055 |
| rs756086312 | snp | A/G | 1.65113e-05 | 0.00287322 | intron-variant | SAE1 | GRCh38.p7 | 19:47155089 | CTAGGGTAAAATTAC[A/G]TTCTCTCCCCTTGTC | 10055 |
| rs756096784 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47171134 | CGCGTGCCACCACAC[A/C]CAGCTAATTTTTATA | 10055 |
| rs756143929 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167521 | CTGGGATTACAGGTG[A/T]GAGCCACTGCGCCCA | 10055 |
| rs756159299 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184467 | CCAGGCTGGAGTGCA[A/G]TGGTGTGATTTTGGC | 10055 |
| rs756169706 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47148696 | CTGGGCTCAATGCAG[C/T]GTCTGCCTCCCAGGT | 10055 |
| rs756195092 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47134467 | AAGGCACCTGGAATA[G/T]ATTGGGAATTAAGTG | 10055 |
| rs756212601 | snp | C/T | 2.08114e-05 | 0.00322572 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209335 | TCATGAAGGCATCTC[C/T]AGGCAAGGAAAACTG | 10055 |
| rs756247133 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47198577 | CTAGGCATCAGGTAG[G/T]AAGTAGCCAACCCAG | 10055 |
| rs756255207 | snp | C/T | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47176242 | TTCCTTTGGATGTAC[C/T]GTCATCTATGACCAG | 10055 |
| rs756257656 | in-del | -/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47200661 | ATAGACAGGCGTCAG[-/C]CACTTGTATCTCTTT | 10055 |
| rs756273086 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47200656 | CTGGGATAGACAGGC[A/G]TCAGCCACTTGTATC | 10055 |
| rs756282055 | in-del | -/TGTGCACCACACTGGGGAGATTGGAGGTAGTTCTGTAGGGA | 1.64762e-05 | 0.00287016 | intron-variant | SAE1 | GRCh38.p7 | 19:47203653 | TGCTCCATTTTCCTT[lengthTooLong]GTCTTCCTCTCTTTT | 10055 |
| rs756397961 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47146583 | TCAGAGCTGCAGTTG[A/T]ATTATCTCATTGAGT | 10055 |
| rs756471984 | snp | C/G | 1.64852e-05 | 0.00287094 | intron-variant | SAE1 | GRCh38.p7 | 19:47143481 | CATCAGGTTAACAAT[C/G]TTTGTCTTACAGGCT | 10055 |
| rs756484180 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47161873 | TATATTGTATGCATG[G/T]TGCCACCTGCTTTTA | 10055 |
| rs756487678 | in-del | -/TTTTT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184798 | TTTGTTTTTGTTTTG[-/TTTTT]GTTTTGTTTTGTTTT | 10055 |
| rs756502635 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47158045 | CTGCCCTTTTGCCTA[A/C]TTGTACAGAATAACT | 10055 |
| rs756515525 | snp | A/C/G | 0.000168546 | 0.00917848 | intron-variant | SAE1 | GRCh38.p7 | 19:47197191 | ATCTCCAAAAAAAAA[A/C/G]AAAAGTGGCTTTATA | 10055 |
| rs756568651 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47189649 | GGAATTGGGGCCGAG[A/G]TGTCTGGCACAGAAA | 10055 |
| rs756671962 | in-del | -/AG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47198132 | TTTTTTTTTTGAGAC[-/AG]AGTTTTGCTCTTGTT | 10055 |
| rs756694220 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47206342 | CTTATTACTGGTCAG[C/T]CTTCAGCCAGCTGGC | 10055 |
| rs756714744 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47131697 | TAGCTTAGGGAATTC[-/T]TTTTTTTTTTTTTTT | 10055 |
| rs756726425 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47188594 | CTTAAGAGCAGTGAC[A/G]GACCTGGAAGATACT | 10055 |
| rs756734245 | snp | G/T | 0.164648 | 0.234979 | intron-variant | SAE1 | GRCh38.p7 | 19:47197197 | AAAAAAAAAAAAAAG[G/T]GGCTTTATAACCTGC | 10055 |
| rs756765448 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47153316 | CTGGAGGCATATTCA[A/G]CCAAAGTCTACCTTG | 10055 |
| rs756855446 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47151808 | CCTTGAACTTGTAGA[C/G]TTAGAGGGTTTGTTA | 10055 |
| rs756855510 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47168101 | GGGGCGCTGAGGCAC[A/G]AGAATTGCTTGAACC | 10055 |
| rs756861021 | in-del | -/TATT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47202285 | GTTTAAAATTATACC[-/TATT]TATTTATTTATTTAT | 10055 |
| rs756943892 | snp | C/T | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47152973 | AATAGCATCAAGTTC[C/T]TTACAGGAGATGTTT | 10055 |
| rs756956828 | snp | C/T | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130709 | TGGGGCTAGGATTGG[C/T]TGGACCCTCCGTCAC | 10055 |
| rs756969362 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47210126 | CAGCTGTTTGTGTTT[C/T]ACATATGTTGTGAAT | 10055 |
| rs756985753 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182363 | GACAGCCACAGGGAA[A/G]TGGGTTCCGATAATG | 10055 |
| rs757001219 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47180889 | GCAGGTTGTACCTCA[C/G]CTGAGTGATGAAATT | 10055 |
| rs757023483 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47159259 | TTTTGACTCCCTCTT[C/T]CTGAGCAATTTGTTG | 10055 |
| rs757062682 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47143899 | GAGGTGTAGAGAAGT[A/G]TTTTTCCAATTTGTG | 10055 |
| rs757146897 | snp | A/C | | | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210971 | ACCCTGTACCTCTAA[A/C]GGCAGAGATTAAGTC | 10055 |
| rs757176164 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47192926 | CATTTCTCTACCCTG[C/T]CCCAAAATGGTTACT | 10055 |
| rs757210154 | snp | A/G | 1.64732e-05 | 0.0028699 | intron-variant, missense, synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47203725 | TGGAGGGATTTTGGC[A/G]CAGGAAATTGTGAAG | 10055 |
| rs757247736 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47161519 | CTGGTACATTTGTGT[A/G]GATTAAAAAAGACAC | 10055 |
| rs757258090 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47158394 | CTTCCTTTGGTGCTC[A/C]GGAGAAGATTTGAGA | 10055 |
| rs757345856 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47172781 | CCAAAAAAAAAAAAG[A/T]GAAAAGAAAAAAAGC | 10055 |
| rs757361599 | in-del | -/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47136757 | GCCTCCCAAAGTGCT[-/G]GGGATTACAGGCATG | 10055 |
| rs757371153 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167929 | TAGGCACAGTGGCTC[A/C]CGCCTATAATCCCAA | 10055 |
| rs757400022 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47169821 | TTTTTTCCACAGAAG[A/G]TGGTCTTCTGCCCTG | 10055 |
| rs757418611 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47186715 | CAAATAGCGAGGCAC[A/G]GCTTCTTTCCCTCTT | 10055 |
| rs757435589 | in-del | -/CA | 1.66164e-05 | 0.00288235 | intron-variant | SAE1 | GRCh38.p7 | 19:47152852 | ATCAGGGCAGTGATT[-/CA]CAGTTTGCAAAACTC | 10055 |
| rs757452746 | in-del | -/AAA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47189574 | TTAAAACGAACAAAC[-/AAA]AAAAACAAAAGTGAG | 10055 |
| rs757486381 | snp | A/C/G | 8.24477e-05 | 0.00642005 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150242 | AGTTCTTGATTCGTA[A/C/G]TGGGTCTGTTGGCCG | 10055 |
| rs757559519 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47165557 | CAGGGGTTCATTCCA[A/G]TGGATAGTGGATGCC | 10055 |
| rs757563371 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47134666 | TAATCGAAGGGGTTT[G/T]CGGCAGCAGATAGCT | 10055 |
| rs757633452 | snp | C/T | 1.65844e-05 | 0.00287957 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209363 | CTGAAGTCATTGGCC[C/T]GATACAAAACATTTC | 10055 |
| rs757649549 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163540 | GGAGACCAGCCTGGC[C/G]AACATGGTGAAACCC | 10055 |
| rs757667918 | snp | A/G | 1.95766e-05 | 0.00312856 | intron-variant | SAE1 | GRCh38.p7 | 19:47150177 | AAAAATACAAGACTT[A/G]AAAAAATATGTGTAT | 10055 |
| rs757668584 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47200924 | GTGCAGTGGCATGAT[C/G]TCGGCTCACTGCAAC | 10055 |
| rs757787698 | snp | C/T | 3.31241e-05 | 0.00406952 | intron-variant | SAE1 | GRCh38.p7 | 19:47197395 | TGGTGTCAGTATTTA[C/T]CACTGTTTAGTCTGG | 10055 |
| rs757811220 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47177013 | AGCATGAACAATAAC[A/T]TACAGGTTTAGCCTA | 10055 |
| rs757842708 | snp | A/G | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191398 | CTGTTAGTATAGCCA[A/G]AGCAGAGGATATTGC | 10055 |
| rs757863297 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47207335 | CCCTGTTTTATGGAT[A/G]AGGAAAAGGGTTTGG | 10055 |
| rs757865755 | snp | C/T | 5.35251e-05 | 0.00517297 | intron-variant | SAE1 | GRCh38.p7 | 19:47150188 | ACTTAAAAAAATATG[C/T]GTATTATTCCTAGGT | 10055 |
| rs757896982 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47175743 | CTCTGTCTCAAAATA[A/C]AATAAATAAAATATC | 10055 |
| rs757916303 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47161264 | GATCCTCTTGCCTTG[A/G]CCTCTCAAAGTGCTG | 10055 |
| rs757926219 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47140834 | TATTTGGTGTTGATG[A/G]CAGTTGAGTATTTAA | 10055 |
| rs758015676 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47154863 | TTTGATTTATTGAGA[A/G]CAGCTGTGTGCCCAG | 10055 |
| rs758043568 | in-del | -/CGTCTTTCCTTTCTTA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47206486 | TGGAATCATCTTTTG[-/CGTCTTTCCTTTCTTA]CGTCCTTCTAGATAC | 10055 |
| rs758066251 | in-del | -/TTTT/TTTTTTTT | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129809 | TCCTTCCTTCCTTTC[-/TTTT/TTTTTTTT]TTTCTTTCTTTCTTT | 10055 |
| rs758066353 | in-del | -/CTT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47168986 | TAGGTCCTAGCCATC[-/CTT]CTGCCTATTACTGGG | 10055 |
| rs758153074 | in-del | -/TATT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47202284 | GTTTAAAATTATACC[-/TATT]TATTTATTTATTTAT | 10055 |
| rs758163216 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47153544 | AGTTTCTGACCACCC[C/G]CTCCAAAACCCTCCA | 10055 |
| rs758350464 | snp | A/C | 1.90489e-05 | 0.00308611 | stop-gained, utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209321 | CCTGTCCCCTTCCTT[A/C]ATGAAGGCATCTCCA | 10055 |
| rs758378974 | in-del | -/C | 1.66222e-05 | 0.00288285 | intron-variant | SAE1 | GRCh38.p7 | 19:47143650 | CTCTGGCTCCCCTTT[-/C]CCAGCATGAAGATCT | 10055 |
| rs758437870 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47158428 | ATTTCGTCACAATCA[A/G]GTCTCGGGCACAAGC | 10055 |
| rs758472087 | in-del | -/C | 3.30901e-05 | 0.00406743 | intron-variant | SAE1 | GRCh38.p7 | 19:47197227 | CTTCTTTTTCTTATT[-/C]CCCAGTGCTCTTAAA | 10055 |
| rs758493315 | in-del | -/GTAT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167689 | TATCTGGTTGGGAGG[-/GTAT]GTATGGAGAGAGAGG | 10055 |
| rs758499437 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47187874 | CTTCTCCCCTAGTTA[C/T]CCTTTATTCTTCAAA | 10055 |
| rs758535198 | snp | G/T | | | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47211043 | CCCAGGCAAGAAATG[G/T]CTAGTTTCTACAAAT | 10055 |
| rs758539906 | snp | C/T | 1.65214e-05 | 0.0028741 | intron-variant | SAE1 | GRCh38.p7 | 19:47143455 | GATTCTGCAAGCTCA[C/T]TGTTCTGTATCATCA | 10055 |
| rs758576503 | in-del | -/TTTT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184819 | TTTTGTTTTGTTTTG[-/TTTT]GTTTTGTTTTGTTTT | 10055 |
| rs758708060 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47136047 | GACCTCGTGTACCAC[A/T]ATTTCTTTATCCATT | 10055 |
| rs758716412 | snp | C/T | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47169833 | AAGGTGGTCTTCTGC[C/T]CTGTTAAAGAAGCCC | 10055 |
| rs758746404 | in-del | -/TT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47195738 | TCCTTTTTTTCTTCT[-/TT]TTTTTTTTTTTTTTT | 10055 |
| rs758786535 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47186979 | GGGGCTGTCTGGGTC[A/G]CTTCTGGGTCCCCAC | 10055 |
| rs758793908 | snp | A/G/T | 1.69e-05 | 0.00290684 | intron-variant | SAE1 | GRCh38.p7 | 19:47150408 | AAATCTGCTGTGGGA[A/G/T]TTAAACAAATTAAGG | 10055 |
| rs758806713 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47202266 | AATAGTTGATAATAT[G/T]TGGGTTTAAAATTAT | 10055 |
| rs758854643 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47145057 | GCCCAGGCTGGAGTG[C/T]AATGGCGTGATCTTG | 10055 |
| rs758880875 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47165777 | AGTTTGAACCAAAAG[G/T]ATTGTTAAGTGGAGT | 10055 |
| rs758993000 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47158186 | GTTTAACCAAAGGTT[A/G]TAAAGCCACTTTTGC | 10055 |
| rs759089137 | in-del | -/A | 1.65427e-05 | 0.00287595 | intron-variant | SAE1 | GRCh38.p7 | 19:47169946 | CTCAAAGCACAACTT[-/A]CCCCGGGAGAGCTTT | 10055 |
| rs759112057 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47194228 | AAGTGCCAGGCTGGT[A/G]GAGTGAATGAATTCT | 10055 |
| rs759126444 | snp | A/G | | | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210718 | GCATCACCTGCTCCC[A/G]CCGGAGGTGAGACAG | 10055 |
| rs759198383 | snp | A/G | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191569 | AGCAGTCACGTGGAA[A/G]CTGAGGCTGCCTGCT | 10055 |
| rs759301337 | in-del | -/CC | 6.7245e-05 | 0.0057981 | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209293 | GCCAACTGCAGCATG[-/CC]CACCTGTATTCCCTG | 10055 |
| rs759301853 | snp | A/G | 3.29582e-05 | 0.00405931 | intron-variant | SAE1 | GRCh38.p7 | 19:47169795 | ATATGTTATTCCTAA[A/G]CAGTTCTGCCTTTTT | 10055 |
| rs759310794 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47186524 | TCCCCTCTGCTGTGG[A/G]TGAGGGTGCAGGTCC | 10055 |
| rs759315250 | in-del | -/TGTGTGTG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137704 | TAACACTCAGCTGAT[-/TGTGTGTG]TGTGTGTGTGTGTGT | 10055 |
| rs759327356 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47185258 | TGGTACAGACTGAGT[A/G]TCTAAATCCAAGAAC | 10055 |
| rs759360566 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47151213 | GGAGTGCAATTGTGC[G/T]ATCTTGGCTCATGGC | 10055 |
| rs759376997 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47201530 | GCACGTGCCACCACG[C/G]CCAGCTAATTTCTGT | 10055 |
| rs759481578 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47178084 | CATCTCTACTAAAAA[G/T]ACAAAAATTAGCTGG | 10055 |
| rs759512709 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47148475 | AATACTTTGAGAGCA[A/G]TATGGAATCTGTAAT | 10055 |
| rs759521722 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47149703 | GCTCTTTAACCATCA[A/G]TGACCAGTTTAAAAA | 10055 |
| rs759609829 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47164431 | CTTGGCCTCCCAAAG[C/T]GCTGGGATTACAGGC | 10055 |
| rs759634241 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163204 | CTTCACATTCATGGA[G/T]TCAACCAACTGTGGA | 10055 |
| rs759646173 | snp | G/T | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191760 | TTTGGTTTGAAAACA[G/T]AGCTGTGGGAATAGG | 10055 |
| rs759696218 | snp | A/G | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176668 | GTTTTTTATTGCCCC[A/G]TTCACAATTCAGCCA | 10055 |
| rs759704984 | snp | C/T | 0.000206462 | 0.0101582 | intron-variant | SAE1 | GRCh38.p7 | 19:47180346 | GAAAGTAAGGAAGTG[C/T]TCTAAGAATGATAGG | 10055 |
| rs759714247 | snp | A/G | 1.64808e-05 | 0.00287057 | intron-variant, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197250 | CTCTTAAAGTTCCGT[A/G]CAGATAAAGGAAGAG | 10055 |
| rs759734818 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47140312 | AGGGTTTCACCTTGT[G/T]AGCCAGGATGGTCTC | 10055 |
| rs759829417 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47148927 | CATAGTCTATCTATG[-/T]TTTTTTAAAAGTTCA | 10055 |
| rs759903572 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47206210 | GCCAGAGTACTCTGC[A/G]TTCTTCGTTGCTGGG | 10055 |
| rs759939395 | in-del | -/ACTCC | | | intron-variant | SAE1 | GRCh38.p7 | 19:47166320 | TTAATCTGGCACAGA[-/ACTCC]TAAGGAGTGTGAAAA | 10055 |
| rs759954524 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163518 | GGATCACTTGAGGTC[A/T]GGAGTTGGAGACCAG | 10055 |
| rs760105245 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47195593 | CCCTTCTGGCTAAAG[A/C]AGGCTTTAAACTGGT | 10055 |
| rs760127440 | snp | C/G | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47152921 | GACTTGCTGCTCCAG[C/G]GATGTCATAGTTAAA | 10055 |
| rs760134458 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47145366 | TGGCCAGGTTGGTCT[C/T]GAACTCCTGACCTCA | 10055 |
| rs760252231 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182219 | GTGATTAGTTCTCTT[C/T]AGAAGAAACTTCTTA | 10055 |
| rs760271626 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47188780 | GCTCTTCGCTGCTGC[C/T]CTCCAGTTGGAAAGC | 10055 |
| rs760298162 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47144430 | TCAGGCCAGGCACAG[A/T]GGCTCATGCCTGTAA | 10055 |
| rs760311447 | snp | A/T | 6.58957e-05 | 0.00573964 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47152946 | GTTAAAGTTGACCAG[A/T]TCTGTCACAAAAATA | 10055 |
| rs760318071 | in-del | -/TG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47168220 | TTTAAAACAAAAAAC[-/TG]TTTTTTTGTATGTGT | 10055 |
| rs760321566 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47173751 | GGATTATGCTAAACT[C/T]AAAGGCCAGTTGACT | 10055 |
| rs760362409 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47199934 | TGTTTAGATGATGGC[-/T]TTTTTTTTTTTTTGG | 10055 |
| rs760383663 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47158985 | AGGATAAAAGGCCAC[C/T]GTCATGCTCCCATGT | 10055 |
| rs760407119 | snp | C/G | 3.3012e-05 | 0.00406262 | intron-variant | SAE1 | GRCh38.p7 | 19:47209155 | TTTTCATTTTTCTCC[C/G]CAGGCCCTGTCTCAG | 10055 |
| rs760457883 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47173216 | GTTGGCCAGGCTGGT[C/G]TCGAACTCTTGACCT | 10055 |
| rs760477848 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47200896 | AAAGTTTCACTTTGT[C/G]ACCTAGGCTAGAGTG | 10055 |
| rs760495109 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47138185 | AGTAGCTGGGATTAC[A/C]GGCGCCTGCTACCGC | 10055 |
| rs760515161 | snp | C/T | 1.64923e-05 | 0.00287156 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SAE1 | GRCh38.p7 | 19:47143525 | GTGCTTCTTGTCGGC[C/T]TGAAAGGACTTGGGG | 10055 |
| rs760585904 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47151351 | AGATGGGGTTTCACC[A/G]TGTTGGTCAGGCTGG | 10055 |
| rs760595435 | snp | A/G | 0.000185787 | 0.00963634 | intron-variant, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47180220 | CGCACTCATGCCAAG[A/G]TGTTAATACCTTTCC | 10055 |
| rs760603971 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47166561 | AAAACACAACCTCCA[C/T]CCCCAACTCCGTTTC | 10055 |
| rs760654593 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47136887 | AGAGCAAATTGACTT[C/G]CCTCTAAGAGGGCTC | 10055 |
| rs760694008 | snp | A/C/G | 4.9433e-05 | 0.00497137 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47169909 | GCACGACCTCCGACT[A/C/G]CTTTCTCCTTCAAGG | 10055 |
| rs760735806 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47204495 | GAGCCACTGTACCCA[A/G]CCGCACCCCCCCCCT | 10055 |
| rs760740884 | in-del | -/AACAAAAACA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47144711 | TTCAACAACAACAAC[-/AACAAAAACA]AACAAAAACAAACAA | 10055 |
| rs760741170 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47150148 | AAAGATTCTTTTTAA[C/G]ATTTATTTTCCCTAA | 10055 |
| rs760769817 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137424 | AAATAAAGTAAAGAA[A/G]CAGCTTCCTAGAGCA | 10055 |
| rs760834806 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47201727 | CAACCTCCACCTCCT[A/G]GGTTCATGCAATTCT | 10055 |
| rs760904459 | snp | G/T | 1.65012e-05 | 0.00287234 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150236 | GAGCTCAGTTCTTGA[G/T]TCGTACTGGGTCTGT | 10055 |
| rs760929705 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47178314 | AAAAATGCGGAGTGC[C/T]TGCTTGTAGCTCACA | 10055 |
| rs761017626 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47192092 | AGAGAAAGAAAATAT[A/G]GCTTTGGGAGCACCA | 10055 |
| rs761017631 | snp | A/T | 1.6477e-05 | 0.00287024 | intron-variant, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197264 | TACAGATAAAGGAAG[A/T]GATCCCAGTTCTGAT | 10055 |
| rs761047560 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184822 | GTTTTGTTTTGTTTT[-/T]GTTTTGTTTTGTTTT | 10055 |
| rs761049067 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163037 | TTCATAATTCCAAAT[A/G]TGGAAAATGCAGAAC | 10055 |
| rs761068454 | snp | C/T | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190974 | TGTCCCTGTATGGAC[C/T]TGCTGTTTCTTTTGG | 10055 |
| rs761079403 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47159941 | TCAAGTGATCCGCCC[A/G]CTTTGGCCTCCCAAA | 10055 |
| rs761261948 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47183537 | TCTTATTCCACTTTT[A/G]CAGATGGGAAACTGA | 10055 |
| rs761277050 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47133547 | GTGTTTTAAAATGAT[C/T]GCTCCAGAATAGGTT | 10055 |
| rs761277967 | snp | G/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47155171 | TGGGCCCGACACCAA[G/T]AGAGCAAAACTTGAT | 10055 |
| rs761329433 | in-del | -/CAT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47135121 | AATGGGTAATAATCA[-/CAT]CAGGGTAAATGGGGT | 10055 |
| rs761331565 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47170313 | TCCACCTCCTGGGTT[A/G]AAGCGATTCTGGTGT | 10055 |
| rs761441588 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47162333 | TGATCTCCTTGGGCA[A/G]TTGTGTTAATTTCTC | 10055 |
| rs761536838 | snp | A/G | 1.66076e-05 | 0.00288158 | missense, utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209282 | GCCCCAGAGATGCCA[A/G]CTGCAGCATGCCCAC | 10055 |
| rs761557764 | snp | C/T | 1.66554e-05 | 0.00288573 | intron-variant | SAE1 | GRCh38.p7 | 19:47153079 | GAACATAACATTTTC[C/T]CCTTTTTATACTTTT | 10055 |
| rs761565298 | in-del | -/TG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47150848 | CTATGTCTGTCTGTC[-/TG]TTTCTCACAGTCACA | 10055 |
| rs761600713 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47161285 | CAAAGTGCTGAGATT[A/G]TAGGCATGAGCCACC | 10055 |
| rs761653172 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47147546 | CAACCTCCGCCTCCT[A/G]GGTTCAAGTGATTCT | 10055 |
| rs761680416 | in-del | -/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47187020 | TAGGGTAGGGGTGGA[-/G]GGGGGGGTGCTCAGG | 10055 |
| rs761690435 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47175184 | TCAGGATGCAGGGTG[A/G]CTTTGGGGGATATCC | 10055 |
| rs761695100 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47173288 | AGGCGTGAGCCACCG[C/T]GCCCGGCCCAAAGTC | 10055 |
| rs761782580 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47139265 | GCCACGATGGTCTCC[A/T]TCTCCTGAACTCATG | 10055 |
| rs761803369 | in-del | -/TTTTTTTTTTTTTTT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47201361 | CTGTTATCTGGTTCC[-/TTTTTTTTTTTTTTT]TTTTTTTTTTTTTTG | 10055 |
| rs761814844 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47152695 | GCAGAACGTGACGGT[C/G]TCATAACTTATATTT | 10055 |
| rs761841238 | snp | A/G | 9.88354e-05 | 0.00702908 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47155172 | GGGCCCGACACCAAG[A/G]GAGCAAAACTTGATT | 10055 |
| rs761883537 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47189517 | AGTGAGCAAAGATCG[C/T]GCCACTGCACTCCAG | 10055 |
| rs761888815 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137264 | GTGGTGGTGGGTGCT[G/T]GTAATCCCAACTACT | 10055 |
| rs761906469 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167726 | GAAAGACACCTCTGT[A/G]AGTTTGAAATTATTT | 10055 |
| rs761973424 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47205765 | CATTTCATCTCCCAC[C/T]GGCCCTATGAGGTAG | 10055 |
| rs761976660 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47151511 | GAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTGC | 10055 |
| rs761989857 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47203827 | CTGTCTTAGACAGCT[A/G]CCTGCTTTCTCTCAC | 10055 |
| rs762031355 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47201077 | GATGGAGTCTTACTC[G/T]GTCACCCAAGCTAGA | 10055 |
| rs762063842 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47166713 | CTGATGGCATTCCCA[A/G]ACCATATTGCAAATG | 10055 |
| rs762071032 | snp | A/T | 3.29565e-05 | 0.00405921 | intron-variant | SAE1 | GRCh38.p7 | 19:47203647 | TTCCCAGTGCTCCAT[A/T]TTCCTTGTCTTCCTC | 10055 |
| rs762087560 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47194003 | TGTGTCTTTTTTTTT[C/T]ACCTGGGCATCTGTG | 10055 |
| rs762097160 | in-del | -/TGGGGGCAGAGGTCAGAAACCC | 2.04188e-05 | 0.00319515 | intron-variant | SAE1 | GRCh38.p7 | 19:47155225 | AAGGTATGTGTAACG[-/TGGGGGCAGAGGTCAGAAACCC]TGGGGGCAGAGGTCA | 10055 |
| rs762152269 | snp | C/G | 3.29734e-05 | 0.00406025 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150245 | TCTTGATTCGTACTG[C/G]GTCTGTTGGCCGAAA | 10055 |
| rs762152332 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47180083 | CATGGTTTCTTATAC[A/G]TAGATGTAGTAATAG | 10055 |
| rs762229009 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47144016 | ATTTAGGTCTGAGGC[A/G]AGCTCAGGAGTATGT | 10055 |
| rs762314330 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47156858 | AGAAGACGATGGTTT[C/G]TGTAGCTAGTGCTGG | 10055 |
| rs762341743 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47156767 | ATATTTGTTAATGTA[A/G]TTTATATTAGGGGCT | 10055 |
| rs762450460 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47158025 | AAGATTCCTTGATTC[A/G]GATGCTGCCCTTTTG | 10055 |
| rs762462018 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210316 | ACCATTCCTGCCACC[A/G]TTTTTTCTGGGTGAT | 10055 |
| rs762479479 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47186490 | CCACATTTTTACATG[C/G]TTCATTGAGCATTCG | 10055 |
| rs762484132 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47135545 | AGGGTCTCTCTGTCG[C/T]GCAGACTAGAGTGCA | 10055 |
| rs762502243 | in-del | -/AA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47142385 | CGAGACTCTGTCTTT[-/AA]AAAAAAAAAAAAAAA | 10055 |
| rs762530915 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47194817 | GCAGTGGCGCGATCT[C/T]AGCTCACTGCAACCT | 10055 |
| rs762594994 | snp | A/G | 1.66607e-05 | 0.00288619 | intron-variant | SAE1 | GRCh38.p7 | 19:47155263 | TGGGGCCTTGGAGGG[A/G]TCAGGCAATGACGAT | 10055 |
| rs762595437 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47192760 | GGCCAGGCTGGTCTC[A/C]AACTCCTGACCTCAA | 10055 |
| rs762719604 | snp | C/T | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47155200 | ATTCTTCTGAGACAA[C/T]GATGGTCAAAAAGGT | 10055 |
| rs762726212 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47133768 | CACCTACCTGGAACG[A/G]TGGAATTGCCATTTT | 10055 |
| rs762731705 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47199605 | CAGAGCCAGACCGTT[A/C]ATCACTTTGAATGCC | 10055 |
| rs762742305 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47198237 | AACTCAGCCTTTTGA[C/G]TAGCTGGGATTACAG | 10055 |
| rs762742696 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47148148 | GTTGAGCCAGGATTT[A/G]AATCAAAGATTGAAT | 10055 |
| rs762860904 | in-del | -/T/TG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137726 | TGTGTGTGTGTGTGT[-/T/TG]GTTGTTTTTTTTTTT | 10055 |
| rs762866795 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47162710 | AAGAAGTAAAATAAG[A/G]CTGGGTGCAGTGGCT | 10055 |
| rs762906859 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47146411 | TTTTTAGTAGTTTAG[A/G]TGAGAGGTGAAAGTG | 10055 |
| rs762927650 | snp | C/T | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190808 | AGTTTTATATGACCA[C/T]GGTCTCCACTTCTCA | 10055 |
| rs762932610 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167275 | CAGATAATTTTTGTA[-/T]TTTTTTTTTTTTTGA | 10055 |
| rs763025619 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47161379 | TGCAGATAATGGAAC[A/C]AAACAAACACTATCC | 10055 |
| rs763096321 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47189574 | TTAAAACGAACAAAC[A/G]AAAAAAACAAAAGTG | 10055 |
| rs763107729 | snp | A/G | 0.000192548 | 0.00981005 | intron-variant | SAE1 | GRCh38.p7 | 19:47180312 | ATTACAGGTGAGCTT[A/G]GAATATCCTGCTATG | 10055 |
| rs763143592 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47154278 | GTATTTTTAGCAGAG[A/G]CGGGGTTTCACTATG | 10055 |
| rs763170640 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47187722 | AGACGGGGTTTCACC[A/G]TGTTGGCCAGGCTGG | 10055 |
| rs763171597 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167803 | ACAGAGTCTATACCA[C/T]GCCTGGCCTAAAATA | 10055 |
| rs763184414 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47205982 | ATGGACCCCAGGGCC[A/G]CTGCCCTTGCATTGT | 10055 |
| rs763194093 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47204609 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 10055 |
| rs763219773 | snp | C/T | 1.64893e-05 | 0.0028713 | synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47152904 | TTTCTGCAGGTGTGT[C/T]TGACTTGCTGCTCCA | 10055 |
| rs763256528 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182066 | ATTGGGATAACAGAC[A/G]TGAGCCACTGCACCC | 10055 |
| rs763263960 | in-del | -/TC | | | intron-variant | SAE1 | GRCh38.p7 | 19:47157142 | CGGCGTTGGAGATTT[-/TC]TTTCTCATTTTGTGT | 10055 |
| rs763269394 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47134310 | AGGAGAATTTAGTTT[A/G]AGGGGGTGGGAGCTT | 10055 |
| rs763291568 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47209067 | TCGACCCCAGTTAAG[A/G]ACCACTGCCCTAGAC | 10055 |
| rs763306240 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47169116 | TTATACCATTCCTCT[A/G]CCAAGAAACATTTAA | 10055 |
| rs763314252 | in-del | -/GTGTGTGTG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137719 | TGTGTGTGTGTGTGT[-/GTGTGTGTG]TTGTTTTTTTTTTTT | 10055 |
| rs763362886 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47131438 | TGGTTCCGTGCTGCA[C/G]ACAGGGGAGACTGGA | 10055 |
| rs763423630 | in-del | -/AAAGAAAAGAA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47193842 | AAAAAAAAAAAAAAG[-/AAAGAAAAGAA]AAAGAAAAAGAAATT | 10055 |
| rs763457207 | snp | A/C | 8.24015e-05 | 0.00641825 | intron-variant | SAE1 | GRCh38.p7 | 19:47203772 | GAGCAGAAAATTGTT[A/C]ACCATGACTTTGTAT | 10055 |
| rs763496774 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47131990 | ACAGGAGTGAGCCAC[C/T]GCGCCAGGACGTCTT | 10055 |
| rs763510116 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47185494 | TATTTTTAGTGGACA[C/T]GAGGTTTCACCGTGT | 10055 |
| rs763543317 | snp | C/T | 3.29516e-05 | 0.00405891 | intron-variant | SAE1 | GRCh38.p7 | 19:47203656 | CTCCATTTTCCTTGT[C/T]TTCCTCTCTTTTAGG | 10055 |
| rs763563615 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47180493 | AAGTGCTAAAATCAA[C/T]GGGGAACAGTTTGCG | 10055 |
| rs763571834 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47144322 | CTGGGCAACAGAGTG[A/T]GACTTTGCCTTAAAA | 10055 |
| rs763624438 | snp | C/T | 9.88403e-05 | 0.00702925 | synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47152963 | CTGTCACAAAAATAG[C/T]ATCAAGTTCTTTACA | 10055 |
| rs763634359 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47194829 | TCTCAGCTCACTGCA[A/G]CCTCCCAGGTTCAAG | 10055 |
| rs763651492 | in-del | -/GTTTCGCCAT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47178665 | TTTAGTGGAGACAGG[-/GTTTCGCCAT]GTTGGCCAGGCTGGT | 10055 |
| rs763679091 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47183259 | CATATTAAATCTTCA[C/T]GACAGCCTTACTAGA | 10055 |
| rs763683088 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47144489 | CAGATCATGAGGTCA[C/G]GAGATCGAGACCATC | 10055 |
| rs763727796 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47131603 | GAGGGGGACGGCCGT[A/G]GGCTCCCGAAAAGGT | 10055 |
| rs763747757 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47195658 | TCTCTCTTCTAGGTC[C/T]CTTCCCCTTTCCCTT | 10055 |
| rs763772529 | snp | A/G | 0.00109391 | 0.0233615 | missense, utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209278 | GGCAGCCCCAGAGAT[A/G]CCAACTGCAGCATGC | 10055 |
| rs763784694 | snp | A/G | | | missense, utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209290 | GATGCCAACTGCAGC[A/G]TGCCCACCTGTATTC | 10055 |
| rs763841924 | snp | C/T | | | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210959 | TCAAACTTTTCCACC[C/T]TGTACCTCTAACGGC | 10055 |
| rs763874511 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47187468 | AGATAGCTTGAACAC[C/T]TTTCAATTCAGTCAG | 10055 |
| rs763930436 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47158330 | ATTCTGATAAATAAG[C/G]GCTTAGGAAAATGCC | 10055 |
| rs764017232 | in-del | -/TTT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47145937 | TTCCCATTCTCAAGG[-/TTT]TTTTTTTTTTTTTTT | 10055 |
| rs764022758 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47172410 | CCTGGGCCCTTTGGG[A/T]GAAGCTTGTTGCTCA | 10055 |
| rs764034013 | snp | G/T | 0.000115353 | 0.00759362 | intron-variant | SAE1 | GRCh38.p7 | 19:47155217 | ATGGTCAAAAAGGTA[G/T]GTGTAACGTGGGGGC | 10055 |
| rs764061634 | snp | A/G | 1.65299e-05 | 0.00287483 | intron-variant | SAE1 | GRCh38.p7 | 19:47143450 | TCTGTGATTCTGCAA[A/G]CTCACTGTTCTGTAT | 10055 |
| rs764068290 | in-del | -/TATC | 1.65608e-05 | 0.00287752 | intron-variant | SAE1 | GRCh38.p7 | 19:47197393 | GTTGGTGTCAGTATT[-/TATC]ACTGTTTAGTCTGGA | 10055 |
| rs764093442 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47150191 | TAAAAAAATATGTGT[A/G]TTATTCCTAGGTAAC | 10055 |
| rs764117601 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47186668 | CAACTTTCATCCGGC[A/G]CCTCGGAACCTCTTC | 10055 |
| rs764172689 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47136900 | TTGCCTCTAAGAGGG[C/T]TCTAGGTGGGATAGG | 10055 |
| rs764181449 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47165251 | CATGCCACCATGTCC[A/G]GCTAATTTTTATATT | 10055 |
| rs764219230 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47156456 | TGCACTCCAGCCTGG[C/T]GACAGAACGAGACTC | 10055 |
| rs764228225 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47151367 | TGTTGGTCAGGCTGG[A/T]CTTGAACCCCTGACC | 10055 |
| rs764246739 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47166564 | ACACAACCTCCACCC[A/C]CAACTCCGTTTCATC | 10055 |
| rs764313237 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47201738 | TCCTGGGTTCATGCA[A/G]TTCTTCCACCTCAGC | 10055 |
| rs764345902 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47198213 | CGCCTGGGTCCAAGC[A/G]ATTCTCCTAACTCAG | 10055 |
| rs764359324 | in-del | -/TT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47139586 | CTGTGAATGTGTATC[-/TT]TTTTTTTTTTTTTTT | 10055 |
| rs764401219 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47200669 | GCGTCAGCCACTTGT[A/G]TCTCTTTTAATTTGG | 10055 |
| rs764403149 | snp | A/G | 2.04756e-05 | 0.00319959 | intron-variant | SAE1 | GRCh38.p7 | 19:47150172 | TCCCTAAAAATACAA[A/G]ACTTAAAAAAATATG | 10055 |
| rs764421450 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47178472 | AGCCTTTGCTTACTC[A/G]TTTATGTTTATTTTA | 10055 |
| rs764456184 | snp | C/G | 4.94287e-05 | 0.00497111 | intron-variant, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197268 | GATAAAGGAAGAGAT[C/G]CCAGTTCTGATACAT | 10055 |
| rs764457461 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47140787 | GTTCACAGAATGAGA[A/C]CCTGTTTCAATAAAA | 10055 |
| rs764507041 | snp | C/T | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176838 | AAAAGGTCTCTTCTT[C/T]TTATTATTCTCCCAT | 10055 |
| rs764509426 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47192159 | CACTATACTAAACAT[G/T]TCACATGGCTTAGCA | 10055 |
| rs764531550 | snp | A/C | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47191260 | TAGTAAAAATACAAA[A/C]GTTATTTGGGCGTGG | 10055 |
| rs764545827 | in-del | -/AGG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47199291 | TCGGGAGGCTGAGGC[-/AGG]AGAATGGCGTGAACC | 10055 |
| rs764608284 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47208311 | GTTCCCCAGGCTGGA[G/T]TATAGTGGCACTATT | 10055 |
| rs764661098 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47153218 | AAAGTGCTGGGATTA[A/T]AGGCATGATCCACTG | 10055 |
| rs764750947 | in-del | -/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47185531 | GGCTGATCCTGAACT[-/C]CTGACCTCAAGTAAT | 10055 |
| rs764807981 | snp | A/C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47154786 | CAGGCGTGAGCCACT[A/C/G]CACCCAGCCAAGTTT | 10055 |
| rs764843727 | in-del | -/TTTCCTAGAATTG | 0.000191186 | 0.00977531 | intron-variant | SAE1 | GRCh38.p7 | 19:47180138 | TTTTACACGTGTTTA[-/TTTCCTAGAATTG]TTTCCTAGAATTGTT | 10055 |
| rs764869157 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163648 | AGGAGAATCACTTGA[A/G]CTTGGGAGGCAGAGG | 10055 |
| rs764878678 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47183770 | GGAATGTCCTGTGCC[A/G]TCTTCCCTCGGCAAG | 10055 |
| rs764885471 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47160867 | GAACTACTTGGTTCA[A/G]AGGAGTGGAAATAGG | 10055 |
| rs764898912 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47147917 | GCGCCCACCACCACG[C/G]CTGGCTAATTTTTTT | 10055 |
| rs765001287 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47161330 | TTTTTTTTATTGTGA[C/T]ATTTAATGCACAAAA | 10055 |
| rs765019403 | snp | G/T | 1.76839e-05 | 0.00297349 | missense, utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209308 | CCCACCTGTATTCCC[G/T]GTCCCCTTCCTTCAT | 10055 |
| rs765078949 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47143395 | CAGGCATGAGCCACC[A/G]TGCCTGGCAAACCAA | 10055 |
| rs765179784 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47159285 | TGTTGACAGCCTTCT[C/T]ATCCTCTCTTACACC | 10055 |
| rs765195833 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47196652 | CAGCTGTGAGCCACC[A/G]CACCCGGCTCTTCCA | 10055 |
| rs765200394 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47175242 | TACTCTTGTTTCCAT[C/G]TTCCTGGCACCTAAG | 10055 |
| rs765286640 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47189530 | CGCGCCACTGCACTC[C/G]AGCCTGGGTGACAGA | 10055 |
| rs765363305 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47195768 | TTTGACAGGGTCTCA[C/T]TCTGTCACCCAGGCT | 10055 |
| rs765421039 | snp | A/G | 4.9423e-05 | 0.00497082 | synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47169823 | TTTTCCACAGAAGGT[A/G]GTCTTCTGCCCTGTT | 10055 |
| rs765509142 | in-del | -/GAAAG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47193841 | AAAAAAAAAAAAAAA[-/GAAAG]AAAAGAAAAAGAAAA | 10055 |
| rs765527301 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47202045 | AGGGCGTAAGGAGCC[A/G]GAGGTGCCTTTGGAC | 10055 |
| rs765563567 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47166736 | TGCAAATGACTTGAT[A/G]TGTATTTTCAGACTT | 10055 |
| rs765596984 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47178765 | GCATGAGCCATCGTG[A/C]ATAGCCTGCGTTTTT | 10055 |
| rs765598152 | snp | C/G | 1.64852e-05 | 0.00287094 | synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150246 | CTTGATTCGTACTGG[C/G]TCTGTTGGCCGAAAT | 10055 |
| rs765657574 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47165705 | CACCTTTTGCATCTG[C/T]TGCTACAGATTAGGC | 10055 |
| rs765684359 | snp | A/G | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129529 | CGAACTCCTGACTTC[A/G]TGATCTGCCCTCCCT | 10055 |
| rs765687312 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47192399 | GATTAAAAGCGTCCG[C/T]CACCATGCCCAGCTA | 10055 |
| rs765699350 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47180089 | TTCTTATACGTAGAT[A/G]TAGTAATAGATGTAT | 10055 |
| rs765739980 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47195739 | CCTTTTTTTCTTCTT[-/T]TTTTTTTTTTTTTTT | 10055 |
| rs765779426 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47158058 | TAATTGTACAGAATA[A/G]CTAGTTGGGTTGTGC | 10055 |
| rs765790794 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47143324 | TGGTCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 10055 |
| rs765811007 | in-del | -/AC | | | intron-variant | SAE1 | GRCh38.p7 | 19:47181831 | TTTTTTTTTTTTAAG[-/AC]AGAGTCTTGCTCTAA | 10055 |
| rs765865484 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47171744 | GTTGGGATTACAGAC[A/G]TGAGCCACTGCACCT | 10055 |
| rs765892567 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47208789 | CTTGAATTCCTGGGC[C/T]CAAGTGATTCTCCCA | 10055 |
| rs765935598 | snp | G/T | 1.64738e-05 | 0.00286995 | intron-variant, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47203679 | CTTTTAGGTACTGCT[G/T]CTCCGAGATGGCCCC | 10055 |
| rs765957755 | in-del | -/AAAAAAA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47192054 | GCGAGACTCTGTCTC[-/AAAAAAA]AAAAAAGAAAAAAGA | 10055 |
| rs765960161 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47141813 | TAAATCCTTTTCAGT[A/G]TGAATAATACATTTG | 10055 |
| rs765971809 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47157044 | GTTAAATTACGCTAA[C/T]GAGGGGATTCTAAAG | 10055 |
| rs765981162 | in-del | -/C | 4.94336e-05 | 0.00497135 | intron-variant | SAE1 | GRCh38.p7 | 19:47169804 | TCCTAAGCAGTTCTG[-/C]CTTTTTTCCACAGAA | 10055 |
| rs765991903 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47170795 | TAAAGGCGTAAGCCA[C/T]CAGTGCTTGTTCCCC | 10055 |
| rs766044817 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47174300 | TCTTTTTTCTTTTTC[-/T]TTTTTTTTTTTTTTG | 10055 |
| rs766085931 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47134196 | AACTAAGTAGAAATA[C/T]GTGAGGGGTTGAGTT | 10055 |
| rs766102353 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47148334 | GGTAGTAAGATAGAG[A/T]GTGTGCTGTGGATGG | 10055 |
| rs766120249 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47207394 | ATGTGTAGCCCCACC[G/T]TCCTCATGAATGATG | 10055 |
| rs766126001 | snp | C/T | 3.33078e-05 | 0.00408078 | intron-variant | SAE1 | GRCh38.p7 | 19:47155264 | GGGGCCTTGGAGGGG[C/T]CAGGCAATGACGATT | 10055 |
| rs766184467 | in-del | -/ATT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47159697 | TTTTAATTTTTAAAA[-/ATT]ATTATTATTTCTGAG | 10055 |
| rs766201975 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47199746 | GCATGACCCAGTCCT[C/T]CTTCCTGCTGCGAAG | 10055 |
| rs766272291 | snp | A/G | 6.07687e-05 | 0.00551187 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209330 | TTCCTTCATGAAGGC[A/G]TCTCCAGGCAAGGAA | 10055 |
| rs766289834 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47198318 | GGGTTTTCCATGTTG[A/G]CCAGGCAGGTCTTGA | 10055 |
| rs766304010 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47145620 | AAGACTTACTCTGTC[A/G]CCCAGGCTGGAGTAC | 10055 |
| rs766378534 | snp | C/T | 0.000389788 | 0.013955 | intron-variant | SAE1 | GRCh38.p7 | 19:47180320 | TGAGCTTGGAATATC[C/T]TGCTATGCCAGAAAG | 10055 |
| rs766415846 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47135777 | CGTGAACAGCAATGC[A/C]CAGCCTTTGTACCAC | 10055 |
| rs766442638 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47178523 | TTTGTTGCCCAGGCT[A/G]GAGTTGCAGGTGCAA | 10055 |
| rs766449585 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47139420 | CGAACTCATGGGCTC[A/G]AGTGATCCTCATGCC | 10055 |
| rs766452105 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47189586 | AACAAAAAAAACAAA[A/C]GTGAGCCAACCCTGG | 10055 |
| rs766466144 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47154357 | CAGCTTCACAAAGTA[C/T]TAGGATTACAGCCAC | 10055 |
| rs766538847 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47142386 | GAGACTCTGTCTTTA[-/A]AAAAAAAAAAAAAAA | 10055 |
| rs766540412 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47206011 | GTCAGCCTTACTTCT[A/G]CACATCCCATTGAGG | 10055 |
| rs766541860 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47138712 | GTGTAGCTTAGCACA[A/G]TGGTGTGTGGCTGTG | 10055 |
| rs766582268 | snp | A/G | 3.29886e-05 | 0.00406118 | intron-variant | SAE1 | GRCh38.p7 | 19:47143472 | GTTCTGTATCATCAG[A/G]TTAACAATGTTTGTC | 10055 |
| rs766584956 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47147787 | TTTTTGAGACAGAGT[C/T]TCGCTCTGTTGCCCA | 10055 |
| rs766603932 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47160064 | TGAATTAACCTTCTA[A/G]TATATTAATTCTCAC | 10055 |
| rs766618485 | snp | A/G | 1.64871e-05 | 0.00287111 | intron-variant | SAE1 | GRCh38.p7 | 19:47169926 | TTTCTCCTTCAAGGT[A/G]AGGTCTCAAAGCACA | 10055 |
| rs766635362 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47175365 | ATTGCCGAAAGTCAT[A/C]TCCGTGGTTTTATAG | 10055 |
| rs766655300 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47188166 | CCAGCCTGGGCAACA[C/T]GGTGAGACCTCGTCT | 10055 |
| rs766761185 | snp | A/G | 1.66601e-05 | 0.00288614 | intron-variant | SAE1 | GRCh38.p7 | 19:47150380 | AATTCGATGCTGTAA[A/G]TTTCTTATTATAAAA | 10055 |
| rs766791387 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47151609 | CCGTTTTTACACTTT[G/T]CTATTTCATATGTGC | 10055 |
| rs766814813 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47204786 | TAGGTGTGAGCCACC[A/G]CACCCGGCCAAGCCC | 10055 |
| rs766837627 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47201519 | TGGGACTATAGGCAC[A/G]TGCCACCACGCCCAG | 10055 |
| rs766844047 | snp | A/T | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130096 | TGCTGAGATTACAGG[A/T]GCGAGTCACCGTGCC | 10055 |
| rs766890028 | in-del | -/TCTCCTGCCTTAG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47185708 | CTGGGTTCAAGTGAT[-/TCTCCTGCCTTAG]TCTCCTGAGTACCTG | 10055 |
| rs766896729 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47205064 | ACATTCTTTGCAGAC[C/T]TTGCTATTTGCCCGA | 10055 |
| rs766922657 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182123 | TCTTTCCTCATTCTT[A/C]AATTTCCCCTCATTC | 10055 |
| rs766930044 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47144351 | AAAGAAATAAATTAA[C/T]GAAAGGTGTTTCAGG | 10055 |
| rs767012340 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47195522 | ATAGTTTTCATAGTA[A/C]AGGAAGTTTTGTTTG | 10055 |
| rs767024453 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47158793 | AGAAATTAAGTGACC[C/T]GACCAAGGCCACACA | 10055 |
| rs767070102 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47143451 | CTGTGATTCTGCAAG[C/T]TCACTGTTCTGTATC | 10055 |
| rs767098367 | snp | A/G | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47152935 | GGGATGTCATAGTTA[A/G]AGTTGACCAGATCTG | 10055 |
| rs767120291 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47158235 | CTCCTAAATTAGTAA[C/T]GTTGAAAAACAAAAA | 10055 |
| rs767153476 | snp | C/T | 1.67189e-05 | 0.00289122 | intron-variant | SAE1 | GRCh38.p7 | 19:47150388 | GCTGTAAGTTTCTTA[C/T]TATAAAATCTGCTGT | 10055 |
| rs767153598 | snp | G/T | 1.67562e-05 | 0.00289444 | intron-variant | SAE1 | GRCh38.p7 | 19:47209111 | TTTTTTTCCCTCTAT[G/T]CCTCTTAAAGCACTT | 10055 |
| rs767172182 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47194254 | ATTCTACTTAGAGAA[C/T]GGCCCTCAACACAGG | 10055 |
| rs767241315 | in-del | -/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184140 | ATAGAATATTGGGCT[-/G]GGGCTAGTCTGAAAT | 10055 |
| rs767276345 | snp | C/T | 1.64735e-05 | 0.00286993 | intron-variant, missense, synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47203683 | TAGGTACTGCTTCTC[C/T]GAGATGGCCCCAGTG | 10055 |
| rs767281924 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47172124 | GGGTTTCACCATGTT[C/G]GCCAGGCTGGCCTCA | 10055 |
| rs767297507 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47201679 | CTCTCTCTCACCCAG[A/G]CTGGAGTGCAGTGGC | 10055 |
| rs767406836 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47136797 | CCCCGGCCTTCACCT[A/G]AGTCTTATAGCAGCT | 10055 |
| rs767423665 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47135817 | TTTTTTTTTTGAAAC[A/G]GAGTCTCGCCGTGTC | 10055 |
| rs767428204 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47185506 | ACACGAGGTTTCACC[C/G]TGTTGGCCAGGCTGA | 10055 |
| rs767483778 | in-del | -/TTTTTTTTTTT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47200400 | ACCAAGCCTGCCTAA[-/TTTTTTTTTTT]TTTTTTTTTTTTTGT | 10055 |
| rs767513193 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47134413 | TTTGATGGGGTGGGG[A/G]GATGTCATCATGAGG | 10055 |
| rs767529946 | in-del | -/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167467 | GGATGGTCTCGATCT[-/C]CTGACCTTGTGATCT | 10055 |
| rs767548956 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163381 | CAATACAATATAACA[A/G]CTGTTTACATAGCAA | 10055 |
| rs767555096 | snp | A/C | 2.1986e-05 | 0.0033155 | intron-variant | SAE1 | GRCh38.p7 | 19:47150158 | TTTAAGATTTATTTT[A/C]CCTAAAAATACAAGA | 10055 |
| rs767565256 | snp | A/G | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176708 | CGCATGCATGTGCTT[A/G]CCATGTTTAGATATT | 10055 |
| rs767606228 | snp | A/G | 1.64795e-05 | 0.00287045 | intron-variant, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197256 | AAGTTCCGTACAGAT[A/G]AAGGAAGAGATCCCA | 10055 |
| rs767613309 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47195127 | TGGCACGATCTCGGC[C/T]CACTGCAACCTCTGC | 10055 |
| rs767623283 | in-del | -/TGTT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137726 | GTGTGTGTGTGTGTG[-/TGTT]GTTTTTTTTTTTTTT | 10055 |
| rs767636216 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47140623 | AGACCCTGTGTCTAC[-/A]AAAAAAAAAAAAAAA | 10055 |
| rs767672616 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47148523 | GGGGATTATATTATC[A/C]TGTCTTTGAGGCTCT | 10055 |
| rs767677987 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47141603 | TCAGCCATGATAAAA[A/G]AGCCTTTTTTTGAGG | 10055 |
| rs767693521 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47171209 | CACTCTCTTGACCTC[C/G]TGATCCGCCCACCTC | 10055 |
| rs767806295 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47175566 | AGATGGTGAAATCCC[A/G]TCTCTACTAAAAAAC | 10055 |
| rs767868466 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47153203 | CCACCTTGGCCTCCC[A/C]AAGTGCTGGGATTAT | 10055 |
| rs767878086 | snp | A/C | 0.00148699 | 0.0272265 | intron-variant | SAE1 | GRCh38.p7 | 19:47197182 | TGAGCCTCCATCTCC[A/C]AAAAAAAAAAAAAGT | 10055 |
| rs767905632 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47189631 | TCAGCTGCAGGGAGC[C/T]AGGGAATTGGGGCCG | 10055 |
| rs767907696 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47207057 | TTCCAGCACTTTGGG[A/C]GGATTGCTTGAACCT | 10055 |
| rs767933422 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47154648 | TACAGGCGCCCACCA[C/T]CACGCCCGGCTAGTT | 10055 |
| rs767963080 | in-del | -/TATT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47142904 | CACATATTATGTATC[-/TATT]TGTTTATCTGTCTCC | 10055 |
| rs767995716 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47206273 | TTGGGAAGCACTTTA[C/T]CTTTTGCCCCATGTC | 10055 |
| rs768011497 | snp | C/G | 3.29457e-05 | 0.00405854 | synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47155162 | AGTAGAAGATGGGCC[C/G]GACACCAAGAGAGCA | 10055 |
| rs768121991 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47197797 | CTCAAGTTGTGTTCA[A/G]GCTTTTCTAACTGCG | 10055 |
| rs768144427 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47176147 | GAACTTGCTTGTGTA[C/T]ACTTGATGGCGTAAA | 10055 |
| rs768157328 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47162255 | TTTATAAGCATTTGG[G/T]TATGCTCATAATTTG | 10055 |
| rs768194857 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47199152 | AGCACTTTGGGAGGC[C/T]GAGACAGGCAGATCA | 10055 |
| rs768249064 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47160851 | CTAATTATTAATATC[A/G]GAACTACTTGGTTCA | 10055 |
| rs768273912 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47147381 | GGCTAATTTTTTGTA[-/T]TTTTTTGTAGAGACT | 10055 |
| rs768344541 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47138198 | ACAGGCGCCTGCTAC[C/T]GCGCCCAGCTAATGT | 10055 |
| rs768390146 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47180762 | CAGGAGGTCGAAGCT[G/T]CAGTGAGTTGTGATT | 10055 |
| rs768392764 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47200185 | TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGTT | 10055 |
| rs768429850 | snp | C/T | 1.65097e-05 | 0.00287308 | intron-variant | SAE1 | GRCh38.p7 | 19:47143623 | GCGCTGTTGTGAGCT[C/T]ATTCCTCCCCTGCTC | 10055 |
| rs768430760 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47152619 | TGTATATGTTCGTGG[A/G]TTACAGAAAACATTT | 10055 |
| rs768441980 | snp | C/T | 1.7009e-05 | 0.0029162 | intron-variant | SAE1 | GRCh38.p7 | 19:47150198 | ATATGTGTATTATTC[C/T]TAGGTAACTCCAGAA | 10055 |
| rs768464948 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47174987 | GTGCTGAGATTACAG[A/G]CGTGAGGCACCGTGC | 10055 |
| rs768487299 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47139135 | TTTTGTATTTTGAGT[A/G]GAGATGGAGTTTCAC | 10055 |
| rs768531956 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47168603 | TCAGCCATAAATGTG[G/T]TGTTGTTGTTGTTTT | 10055 |
| rs768541280 | snp | A/G | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190371 | TTTGGCTCTTGGGGC[A/G]GGGCGGAAAGCAGAA | 10055 |
| rs768556572 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47189418 | GTATATAAATGAGCC[A/G]GGCGTAGTGGTGCGT | 10055 |
| rs768561660 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant, missense, intron-variant | SAE1 | GRCh38.p7 | 19:47130871 | GCGGTAGGTGGCGCG[C/T]GGGTCCGGCGGGCGG | 10055 |
| rs768563515 | snp | G/T | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190546 | GCTTCTGTTTGTTTT[G/T]CTGCAAGTAAGTGGC | 10055 |
| rs768566472 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47150725 | AAATGTTTTCTTCCG[-/A]AAACTTAACAAGTTG | 10055 |
| rs768620981 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184812 | TTTTTGTTTTGTTTT[-/T]GTTTTGTTTTGTTTT | 10055 |
| rs768629382 | snp | C/T | 8.30806e-05 | 0.00644464 | intron-variant | SAE1 | GRCh38.p7 | 19:47197222 | ACCTGCCTTCTTTTT[C/T]TTATTCCCAGTGCTC | 10055 |
| rs768631480 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47206456 | GGAGATGGGTCAAGC[A/G]CAAGTCTGCTCCTTT | 10055 |
| rs768647909 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47205686 | CGACACCACCAATAA[C/T]AGACAAGACTTACTG | 10055 |
| rs768691417 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167613 | GCCTGGTAACTGATA[C/G]ATCTTGGTTCACTTA | 10055 |
| rs768712854 | in-del | -/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167077 | CTCCCTCAGCTTCCT[-/G]AGCAGCTGGGATTAC | 10055 |
| rs768739969 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47203519 | AGATTTCATTTTCAC[A/G]CCTAGATGCCAGCAT | 10055 |
| rs768779347 | snp | A/G | 1.6476e-05 | 0.00287014 | intron-variant | SAE1 | GRCh38.p7 | 19:47203743 | GGAAATTGTGAAGGT[A/G]AAACATCACTGTGGA | 10055 |
| rs768781292 | snp | C/T | 1.65452e-05 | 0.00287616 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150362 | CAGAGTCATTTTTCA[C/T]TCAATTCGATGCTGT | 10055 |
| rs768828005 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47180024 | GGAAAGGCTAGAAGG[A/G]GCCATGTGGTATTGG | 10055 |
| rs768834184 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47203645 | TGTTCCCAGTGCTCC[A/G]TTTTCCTTGTCTTCC | 10055 |
| rs768882392 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47193962 | TCTGACATTGGCACT[G/T]AGAAAAGCATAGCCC | 10055 |
| rs768888858 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47144868 | GACGAGTCTTGCTGT[G/T]ATGCCCAGACTGGAG | 10055 |
| rs768917077 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47172944 | GGCTCAGGGAATTTA[A/G]AGTCAGTGGCTCAAG | 10055 |
| rs768942015 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47139937 | CCACTTGGGTATTTC[-/T]TTTTTTTTTTTTTTT | 10055 |
| rs768972282 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47210031 | CCCTTTTAACAGAAC[C/T]CCAGTCACATGCGGC | 10055 |
| rs769129980 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47159551 | AGATTATTTTCTTCC[-/T]TTTTTTTTTTTTTTC | 10055 |
| rs769137036 | in-del | -/TT | 9.73402e-05 | 0.00697572 | intron-variant | SAE1 | GRCh38.p7 | 19:47153091 | TTCTCCTTTTTATAC[-/TT]TTTTTTTTTAAATTA | 10055 |
| rs769140605 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47143008 | CATAGTTGGTACTCA[A/G]TAAATATTTGTTGAA | 10055 |
| rs769153313 | in-del | -/TTT | 1.66418e-05 | 0.00288455 | intron-variant | SAE1 | GRCh38.p7 | 19:47209130 | TTAAAGCACTTGAGC[-/TTT]TAAACCCTCTTTTCA | 10055 |
| rs769182254 | snp | A/G | 1.65575e-05 | 0.00287724 | intron-variant | SAE1 | GRCh38.p7 | 19:47155251 | GGTCAGAAACCCTGG[A/G]GCCTTGGAGGGGTCA | 10055 |
| rs769191913 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47136397 | CCCTCCTTGGCCCCC[C/G]AAAGTGTTGCAATTA | 10055 |
| rs769192795 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47149423 | TGATCCTCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 10055 |
| rs769246296 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184802 | TTTTTGTTTTGTTTT[G/T]GTTTTGTTTTGTTTT | 10055 |
| rs769285479 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47187938 | TGCTATGGGGCAAGC[C/T]CTGTGCCAGGTGTTC | 10055 |
| rs769338342 | in-del | -/GCCACCACGC | | | intron-variant | SAE1 | GRCh38.p7 | 19:47139100 | GGACTACAGGCACGT[-/GCCACCACGC]GCCACCACGCCTGGC | 10055 |
| rs769349387 | snp | A/G | 1.66128e-05 | 0.00288204 | intron-variant | SAE1 | GRCh38.p7 | 19:47155260 | CCCTGGGGCCTTGGA[A/G]GGGTCAGGCAATGAC | 10055 |
| rs769357807 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47201032 | CCAGCTATTTTTTTT[A/T]ATTTTTTTATTTTTT | 10055 |
| rs769371933 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47199590 | TGCTGGCCGGTGATG[C/G]AGAGCCAGACCGTTC | 10055 |
| rs769390869 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47145825 | CACCCATCTTAGAGC[A/G]TATTATGTAGTTTAC | 10055 |
| rs769463700 | in-del | -/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47148868 | ATCTGCCTGCCTCGG[-/C]CTCCCAAAGTGCTGG | 10055 |
| rs769600121 | snp | A/G | 1.64735e-05 | 0.00286993 | intron-variant, synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197318 | GTTGCTCCAGATACG[A/G]AATGATGTGCTTGAC | 10055 |
| rs769620608 | in-del | -/GTGTGTG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137719 | TGTGTGTGTGTGTGT[-/GTGTGTG]TGTTGTTTTTTTTTT | 10055 |
| rs769639348 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47206581 | TCTCTCCATCCCCAC[C/T]GTCCACGGCAGGTCT | 10055 |
| rs769648596 | in-del | -/CTCA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184852 | TGTTTTTGAGACAGT[-/CTCA]CTCTGTCCCCCAGGC | 10055 |
| rs769649457 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47177637 | AGTTTCCCAAAGAGG[C/G]ACTATAGGAAAGCAC | 10055 |
| rs769656956 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47165077 | GGCATGAGCCAAGTC[-/T]TTTTTTTTTTTTTTT | 10055 |
| rs769664486 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47141126 | CCTGCCTCACTGTCC[C/T]GAGTAACTGGGACTA | 10055 |
| rs769669563 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47139320 | GTGCTGGGATTACAG[A/G]CGTGAGTCGCCGCGC | 10055 |
| rs769678633 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47177772 | TTTGGGGAGTTGTGA[A/C]GTCTTGACAGAGGAG | 10055 |
| rs769783523 | snp | C/T | 1.66966e-05 | 0.00288929 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150208 | TATTCCTAGGTAACT[C/T]CAGAAGATCCCGGAG | 10055 |
| rs769787809 | snp | A/G | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190588 | GCCCCCTTCCCAGAG[A/G]CCCTGCAAGGACTTC | 10055 |
| rs769899484 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137015 | TGTACAAATTGTGGG[A/G]CATTTTATAAGACAG | 10055 |
| rs769954135 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47205867 | GAGTGTGGTGCCAGG[A/G]TGTGGGCCCAGGCAG | 10055 |
| rs769962069 | in-del | -/T | 1.65637e-05 | 0.00287777 | intron-variant | SAE1 | GRCh38.p7 | 19:47153073 | GGGGAGAACATAACA[-/T]TTTTCTCCTTTTTAT | 10055 |
| rs769964808 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167756 | TGCATCCCCCCCACC[A/G]CCCACCACCAACCTT | 10055 |
| rs769978634 | snp | C/T | 1.64762e-05 | 0.00287016 | synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47153014 | TGGATACACATTTGC[C/T]AATCTAGGAGAGCAT | 10055 |
| rs770010226 | snp | C/G | 1.64798e-05 | 0.00287047 | intron-variant | SAE1 | GRCh38.p7 | 19:47203762 | CATCACTGTGGAGCA[C/G]AAAATTGTTAACCAT | 10055 |
| rs770015294 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182912 | ACATAGCAACACCCT[A/G]TCTCTTTTTTTGACT | 10055 |
| rs770016548 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47133060 | GGGAGAACTTTCCTA[A/G]CTAAGAGAACAGCAA | 10055 |
| rs770030735 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47181988 | GAGAGGCCTCACTCC[A/G]TGGCCTAGGCTGGTC | 10055 |
| rs770046939 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47155991 | TGGTCCACCTGCCTC[A/T]GCCCCACAAAGTGCT | 10055 |
| rs770155669 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47173656 | TACTCACTAGATGCC[A/G]GTAATATCTCCCCAC | 10055 |
| rs770168736 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47197391 | AGGTTGGTGTCAGTA[C/T]TTATCACTGTTTAGT | 10055 |
| rs770181441 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47131159 | GTGCTCTGGGATCGT[C/T]TCTCTCTTGGGGGGA | 10055 |
| rs770207339 | snp | C/G/T | 3.29518e-05 | 0.00405894 | intron-variant | SAE1 | GRCh38.p7 | 19:47203654 | TGCTCCATTTTCCTT[C/G/T]TCTTCCTCTCTTTTA | 10055 |
| rs770269710 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47133671 | GGGTCAAATAAATAT[A/T]TTCTGGATATATTTT | 10055 |
| rs770291070 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47158696 | AGTTGCAGAATGCCT[A/G]CTGTGTGCAAGGCAC | 10055 |
| rs770339472 | in-del | -/CA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182503 | GTGTGTGTGCGCGCA[-/CA]CGCACGCGCGCGCGC | 10055 |
| rs770360566 | snp | A/G | 0.000108974 | 0.00738073 | synonymous-codon, nc-transcript-variant, intron-variant | SAE1 | GRCh38.p7 | 19:47130984 | GGAGGAGGCGGCACA[A/G]TATGACCGGCAGATC | 10055 |
| rs770367842 | snp | A/C/G/T | 4.94201e-05 | 0.00497074 | missense, nc-transcript-variant, utr-variant-5-prime | SAE1 | GRCh38.p7 | 19:47143508 | GGCTGCGGGCCTCTC[A/C/G/T]GGTGCTTCTTGTCGG | 10055 |
| rs770376716 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47136641 | GCTGGGATTACAGGC[A/G]TGTGCCACCATGCCC | 10055 |
| rs770402217 | in-del | -/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47170206 | CAGATTGAGAAACCT[-/C]TTTTTTTTTCTTTTT | 10055 |
| rs770416011 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137863 | CCTCTGGAGTAGCTC[A/G]GATTACAGGCGCGTG | 10055 |
| rs770446565 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47173027 | GATTCCAAAGGTCTT[A/G]TTCTTTTTCTTTTTC | 10055 |
| rs770452917 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210431 | GGCTATTTTCAGTGG[C/T]AAGAATTATAATAAT | 10055 |
| rs770492448 | snp | G/T | 8.27986e-05 | 0.0064337 | intron-variant, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47131043 | GGTCAGGGCCGGCGC[G/T]GCTTGAGGCCGCTAG | 10055 |
| rs770498601 | snp | A/G | 3.31912e-05 | 0.00407363 | intron-variant | SAE1 | GRCh38.p7 | 19:47169957 | ACTTACCCCGGGAGA[A/G]CTTTTGGCTCTGATT | 10055 |
| rs770500654 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47203124 | GAGGGGCAGGTGACT[C/G]TGTCATCTAAAATTT | 10055 |
| rs770525576 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47179381 | ACATGGTGGCACACT[C/T]CTATAATCCTAGCTA | 10055 |
| rs770551564 | snp | A/C | 1.64735e-05 | 0.00286993 | synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47169877 | GAGCAGTGAGAAAGC[A/C]AAGGCTGCTCTGAAG | 10055 |
| rs770618814 | in-del | -/TT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47136495 | ATTTTTACCCGAGTC[-/TT]TTTTTTTTTTTTTTT | 10055 |
| rs770676958 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47158785 | AAGCTATGAGAAATT[A/C]AGTGACCTGACCAAG | 10055 |
| rs770708654 | in-del | -/GTT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47197787 | TGCCTGCTCACTCAA[-/GTT]GTGTTCAGGCTTTTC | 10055 |
| rs770730105 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47177921 | TGGAGCTTGGAGAGA[A/G]CAGGCTAGTGGTTTC | 10055 |
| rs770753726 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47151162 | TTTTGCACCTTTTTT[A/T]ATTTGAGATGGAGTT | 10055 |
| rs770759038 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47149528 | TCCTTTAAACTACTT[G/T]TGTATTTCCCCAAAT | 10055 |
| rs770772861 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47173846 | CTGGAGTGCAGTGGT[A/G]CAATCTCAGCTCACT | 10055 |
| rs770793395 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47200747 | TTTATTGGCACACTT[A/G]CTCATTTATATATTA | 10055 |
| rs770797534 | snp | A/G | 3.29696e-05 | 0.00406001 | synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150339 | CACTGAGGATATAGA[A/G]AAGAAACCAGAGTCA | 10055 |
| rs770867774 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47202684 | TTTGGGAGGCCGAGG[C/T]GGGCGGATCACGAGG | 10055 |
| rs770891514 | snp | C/T | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191746 | AAAGCTTTTCATCTT[C/T]TGGTTTGAAAACATA | 10055 |
| rs770895160 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47142478 | ATACTTAACTAGTGC[C/T]TCTTCTCAGCACCTC | 10055 |
| rs770983121 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47141432 | CAGGCATGAGTCACC[A/G]GGCCCGGCTGAATAA | 10055 |
| rs771000371 | snp | A/G | 6.60415e-05 | 0.00574599 | intron-variant, synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197234 | TTTCTTATTCCCAGT[A/G]CTCTTAAAGTTCCGT | 10055 |
| rs771064720 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47207882 | CTCAAGTGATTCTCC[C/T]GCCTCGGCCTCCCTA | 10055 |
| rs771106649 | snp | C/T | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190824 | GGTCTCCACTTCTCA[C/T]CCACTGAACTTACAG | 10055 |
| rs771131329 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47170109 | TACCATTGAGCTCTG[G/T]GTTCTAATGACTTCT | 10055 |
| rs771139132 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47133368 | GTAGCTGGGACTATC[A/G]GCATGTGCCACAACA | 10055 |
| rs771151843 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184536 | CTGCCTCAACTTCCC[A/G]AGTAGCTGGGATGAC | 10055 |
| rs771173417 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47169262 | TTTTGTTTTGGTTTT[C/T]TTGAGGAGTCTTACT | 10055 |
| rs771209124 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47133150 | CCAAATGATTTGAGG[A/G]GTAGCTTTTATTCTA | 10055 |
| rs771210840 | snp | A/C | 1.6498e-05 | 0.00287206 | intron-variant | SAE1 | GRCh38.p7 | 19:47155097 | AAATTACATTCTCTC[A/C]CCTTGTCACCCTCTA | 10055 |
| rs771226832 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47146906 | TATCTGAGAGAAAAC[A/G]GCTGGTGGGCAGTAC | 10055 |
| rs771380674 | snp | A/G | 3.29603e-05 | 0.00405944 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47152919 | CTGACTTGCTGCTCC[A/G]GGGATGTCATAGTTA | 10055 |
| rs771395236 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184694 | GGGATTACAGGCGTG[A/G]GCCACCACTGCCGGC | 10055 |
| rs771432985 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163435 | CTAGAGATGATTTAA[A/T]GTATATGGGAGGCCA | 10055 |
| rs771443450 | snp | C/T | 0.000115398 | 0.00759512 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209262 | AGTGAACTCAAGATT[C/T]GGCAGCCCCAGAGAT | 10055 |
| rs771473587 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47162073 | CACATGTGGCCATTG[A/G]CATCTGTATTGCATA | 10055 |
| rs771483380 | snp | A/T | 3.29457e-05 | 0.00405854 | missense, utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209221 | TGGCATGAAGGGGAA[A/T]GGGATTGTGGAGTGC | 10055 |
| rs771495508 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47197616 | TCAAAATTCAAGGCA[A/G]TGTAAGATCTGTAAA | 10055 |
| rs771498984 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47199390 | GGGAGACTCCTTCTC[-/A]AAAAAAAAAAAAAAA | 10055 |
| rs771517479 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47145156 | TACAGGCATGCAACA[C/T]CATGCCTGGCTAATT | 10055 |
| rs771530429 | snp | C/T | 1.64825e-05 | 0.00287071 | intron-variant | SAE1 | GRCh38.p7 | 19:47203774 | GCAGAAAATTGTTAA[C/T]CATGACTTTGTATAT | 10055 |
| rs771547852 | snp | C/T | 0.000346178 | 0.0131518 | intron-variant | SAE1 | GRCh38.p7 | 19:47143609 | GATCACGAACAGGTG[C/T]GCTGTTGTGAGCTCA | 10055 |
| rs771586599 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47188803 | TGGAAAGCTGTCCAG[A/G]CCAGGGACAGGCTTT | 10055 |
| rs771609964 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182804 | TTACTGGTTACAGGC[A/G]GGGTGTGGTGGCTCA | 10055 |
| rs771650734 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47200360 | ATCTCGGCCTCTTGC[A/G]TAGCTGGGACTATAG | 10055 |
| rs771657558 | in-del | -/T | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129301 | TGGGCATGGTGGCTT[-/T]TTTTTTTTTTTTTTT | 10055 |
| rs771657911 | snp | A/G | | | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210970 | CACCCTGTACCTCTA[A/G]CGGCAGAGATTAAGT | 10055 |
| rs771667957 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47173076 | CTCTATCACCCAGGT[A/T]GGAGTGCAGTGGGGC | 10055 |
| rs771728428 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47139057 | GGAGCAAGGATGATG[A/T]TCTCTAGGATCAGCC | 10055 |
| rs771773534 | in-del | -/AAG | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191327 | TCCATCTCAAAAAAA[-/AAG]AAGAAAAACAAAAAC | 10055 |
| rs771838913 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47177731 | AATTTATTATGGGAA[A/C]TTAGGAAACTGAAGG | 10055 |
| rs771863293 | in-del | -/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47185373 | GTGCGGTGGTGTGTC[-/G]GGCTCACTGCGACCT | 10055 |
| rs771881492 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47187418 | ATTCCATGTGTAGCA[C/T]GTTTGTAACACTTGA | 10055 |
| rs771903878 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167556 | ACAATTTGAACTTTT[A/G]TCTGTCAAATCTATA | 10055 |
| rs771905105 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47150861 | TCTGTTTCTCACAGT[C/T]ACATTGACCATGTTG | 10055 |
| rs771985163 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47143937 | ATGACCTGAGTGACT[A/C]ACTGAAAATGCAGAG | 10055 |
| rs771992457 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47151276 | TGCCTCAGCCTCCCA[A/G]GTAGCTAGGATTACA | 10055 |
| rs771999715 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47181272 | GGTGAGCCGAGATCG[C/T]GCCATTGCACTCCAG | 10055 |
| rs772016035 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47179875 | AGGTTTGTTTTTCAC[A/C]GTGATAGGGGTTAGC | 10055 |
| rs772074418 | snp | G/T | 1.64811e-05 | 0.00287059 | intron-variant | SAE1 | GRCh38.p7 | 19:47203628 | TGTCATGGTCACAGT[G/T]CTGTTCCCAGTGCTC | 10055 |
| rs772093487 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47162551 | TTGTCATTTGTTAGA[A/G]TACTTTGTTAAAGCT | 10055 |
| rs772201298 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47193242 | TTTTTGGTATTTTTA[A/G]TAGAGATGGGGTTTC | 10055 |
| rs772215759 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209727 | CCCAGGCCCCATGAG[A/G]CACCAGTGGAAGCAC | 10055 |
| rs772222535 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47142853 | GCGTTCTCCATCATT[C/G]TTGATTCTTGTCACA | 10055 |
| rs772255583 | snp | C/T | 1.64741e-05 | 0.00286998 | intron-variant, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197334 | AATGATGTGCTTGAC[C/T]CACTGGGTATTAGTC | 10055 |
| rs772305443 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47207942 | AGCCCAGCCCTGTTC[G/T]TGTATTTTAAAGTGC | 10055 |
| rs772312425 | in-del | -/GG/GTGG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182492 | TGTGTGTGTGTGTGT[-/GG/GTGG]GTGTGCGCGCACGCA | 10055 |
| rs772383876 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47157765 | CATTGTTAGTCAGCT[A/G]TTACACTTGAACAAT | 10055 |
| rs772480094 | in-del | -/TTTTG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47153393 | GACCTCATCCTCTCA[-/TTTTG]AACACTGAGGCTGCA | 10055 |
| rs772528576 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47142370 | GCCTGGGCAACAGAG[C/T]GAGACTCTGTCTTTA | 10055 |
| rs772537235 | in-del | -/ACA | 1.64757e-05 | 0.00287012 | cds-indel, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209184 | AGCGGGACCCTCCTC[-/ACA]ACAACTTCTTCTTCT | 10055 |
| rs772559005 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47171302 | AATTTTTATTTTAAT[A/T]TTTTTTTTGGAGACG | 10055 |
| rs772577285 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47170243 | TTTGAGACAGAGTCT[C/T]GCTCTGTCACCCAGA | 10055 |
| rs772599545 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47200484 | TTAAAGTTATGAACC[A/G]CATAACAAGAGAGTA | 10055 |
| rs772619243 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47149235 | GAGTACAGTGGTGCA[A/G]TCGCAGCTCACTGCA | 10055 |
| rs772632494 | snp | C/G/T | 3.2948e-05 | 0.00405871 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47155122 | CCTCTAGGGAGAAAA[C/G/T]TAAAGTTGCCAAAGT | 10055 |
| rs772669216 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184732 | TGTCGTATTTTTTTA[C/T]GTAGGAGAGCTCAGT | 10055 |
| rs772789167 | snp | A/G | 3.32613e-05 | 0.00407793 | intron-variant | SAE1 | GRCh38.p7 | 19:47155262 | CTGGGGCCTTGGAGG[A/G]GTCAGGCAATGACGA | 10055 |
| rs772867920 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47149438 | GGCCTCCCAAAGTGC[A/T]GGGATTACAGGTGTG | 10055 |
| rs772905173 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47152331 | CTGAATGGAAGGTCA[A/C]TTGGTCTGTAACCTT | 10055 |
| rs772906092 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47199601 | GATGCAGAGCCAGAC[C/T]GTTCATCACTTTGAA | 10055 |
| rs772912781 | snp | A/G | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47155199 | GATTCTTCTGAGACA[A/G]CGATGGTCAAAAAGG | 10055 |
| rs772929999 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47162421 | CCGTTAAGTTACTCT[C/T]AAGTGGTTTTATCAA | 10055 |
| rs772980623 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47142504 | ACCTCTTCTGCTGTC[A/T]TGCTAGTTTGAGCCA | 10055 |
| rs772995901 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47155631 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 10055 |
| rs773033582 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47164074 | GCACCTGGCTTGTAT[A/G]TGTGTATATATATGT | 10055 |
| rs773056047 | in-del | -/AG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47185625 | TTGTTTTTTTGAGAC[-/AG]AGTCTCACTGTGTCT | 10055 |
| rs773066346 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47138733 | TGTGGCTGTGATCCC[A/C]GCTACTGGGGAGGCT | 10055 |
| rs773068148 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47141142 | GAGTAACTGGGACTA[C/T]AGGCGCCTGCCACCA | 10055 |
| rs773120031 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163252 | GCTTGGAGTACATCC[-/A]AAAAAAAAAAAAGAA | 10055 |
| rs773142523 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47205242 | TTTGGAGGCCAGCCC[-/T]TAACACTTTGTCTTG | 10055 |
| rs773187175 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47177890 | AGCAGGATAGAGGCT[A/G]AGCCTCGGAGGGGAC | 10055 |
| rs773243454 | snp | A/T | 1.64738e-05 | 0.00286995 | intron-variant, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197323 | TCCAGATACGAAATG[A/T]TGTGCTTGACTCACT | 10055 |
| rs773279602 | snp | A/G | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47176455 | CTATTGCCTAATGGC[A/G]CACATAGTAGGTGCT | 10055 |
| rs773293914 | snp | A/G | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190765 | TCCTAAGAGGAAGCT[A/G]GTTTACTCTCTCAAG | 10055 |
| rs773296249 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47168933 | TCAAAGTAAAATATA[A/T]GTCATTGCATTTATC | 10055 |
| rs773301608 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47206587 | CATCCCCACCGTCCA[C/T]GGCAGGTCTCCCTGT | 10055 |
| rs773308439 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182939 | GACTGTTTTTTTGAA[A/T]CAGTCTCGTTCTGTC | 10055 |
| rs773323987 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47154191 | CACCTCCTGGATTCA[A/G]GTGGTTCTCCTGCTT | 10055 |
| rs773364037 | snp | C/T | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130678 | ACGCCCTCGGGGCCT[C/T]AAGCCGCGCCATTTT | 10055 |
| rs773364244 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47162813 | CTGGGCAATGTGGCT[A/G]AAACCCCTTCTCTAC | 10055 |
| rs773382952 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47143109 | TTAGAACCAAAATGA[-/T]TTTTTTTTTTTTTGA | 10055 |
| rs773385683 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47189566 | ACTCTGTCTTAAAAC[A/G]AACAAACAAAAAAAA | 10055 |
| rs773418783 | in-del | -/CTT | 4.94222e-05 | 0.00497078 | cds-indel, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209191 | CCCTCCTCACAACAA[-/CTT]CTTCTTCTTCGATGG | 10055 |
| rs773468213 | snp | C/G | 3.3264e-05 | 0.0040781 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150374 | TCACTCAATTCGATG[C/G]TGTAAGTTTCTTATT | 10055 |
| rs773644348 | snp | C/T | 0.000131835 | 0.00811788 | intron-variant | SAE1 | GRCh38.p7 | 19:47203767 | CTGTGGAGCAGAAAA[C/T]TGTTAACCATGACTT | 10055 |
| rs773688445 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47131173 | TCTCTCTCTTGGGGG[A/G]ACTGGAGGAGTTGAT | 10055 |
| rs773707681 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47160075 | TCTAGTATATTAATT[A/C]TCACGGTTTAGGTTA | 10055 |
| rs773773815 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47192358 | TGGGTTTGAGCGACT[C/T]CTGCCTCAGGCTCCC | 10055 |
| rs773823281 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47195285 | GTCTCGAACTCCTGA[C/T]CTCAGATGATCCACC | 10055 |
| rs773891502 | in-del | -/CA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182502 | GTGTGTGTGTGCGCG[-/CA]CGCACGCGCGCGCGC | 10055 |
| rs773917899 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47169893 | AAGGCTGCTCTGAAG[C/T]GCACGACCTCCGACT | 10055 |
| rs773927636 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210440 | CAGTGGCAAGAATTA[C/T]AATAATAAAGGGAAG | 10055 |
| rs773965202 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47158073 | ACTAGTTGGGTTGTG[C/T]TCAGAGAGTGCAGGG | 10055 |
| rs773972952 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47201475 | CTCCCAGCTTTAAGT[G/T]ATTCTTTTGCCTCAG | 10055 |
| rs773977877 | snp | A/G/T | 0.000130387 | 0.00807318 | intron-variant, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47131054 | GCGCGGCTTGAGGCC[A/G/T]CTAGGGTCTGGAGGG | 10055 |
| rs773984303 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47187328 | AAAGTGGGACTCCTA[C/T]TGGGTTTCCCTGTTG | 10055 |
| rs773992217 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47172045 | CGCCTCAGCCTCCCG[A/G]GTAGCTGGGATTACA | 10055 |
| rs774064195 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47203130 | CAGGTGACTGTGTCA[C/T]CTAAAATTTGTCCTC | 10055 |
| rs774314226 | snp | A/T | 1.64912e-05 | 0.00287147 | intron-variant, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197242 | TCCCAGTGCTCTTAA[A/T]GTTCCGTACAGATAA | 10055 |
| rs774323972 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47166257 | GGGACAGAGCCAGGC[A/T]TGGGAAGAGAAGTGG | 10055 |
| rs774330131 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47149600 | CCACTGTTAATCAGT[C/T]ATTTGTTAGCAGTTA | 10055 |
| rs774341154 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47150762 | AATTTCTGTGGCAGC[A/G]GCATTTTTTTGTTAG | 10055 |
| rs774375508 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47155231 | ATGTGTAACGTGGGG[G/T]CAGAGGTCAGAAACC | 10055 |
| rs774388378 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47142559 | GTGACATCTTCCTAC[C/T]CCCATGGCTTTCCAT | 10055 |
| rs774396929 | snp | A/G | 9.89054e-05 | 0.00703157 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150340 | ACTGAGGATATAGAG[A/G]AGAAACCAGAGTCAT | 10055 |
| rs774420217 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47164384 | GTGTTAGCTAGGATG[A/G]TCTCCATCTGCTGAC | 10055 |
| rs774420818 | in-del | -/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47199817 | CCTCCACCAAGAGAT[-/G]AGTGCCCCAGTGAGT | 10055 |
| rs774437756 | snp | A/G | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191759 | TTTTGGTTTGAAAAC[A/G]TAGCTGTGGGAATAG | 10055 |
| rs774465944 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47170170 | GTCAAGTTGACCTTA[C/T]GGTAATAGTGTTACA | 10055 |
| rs774481613 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47141446 | CGGGCCCGGCTGAAT[A/C]ATGAATTTTAAACAA | 10055 |
| rs774494811 | snp | C/T | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190576 | CTGGACTGATTGGCC[C/T]CCTTCCCAGAGGCCC | 10055 |
| rs774511548 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137541 | TTACCCAGGCTGGAG[C/T]GCAGTGACGCAGTGA | 10055 |
| rs774524549 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47207888 | TGATTCTCCCGCCTC[A/G]GCCTCCCTAAGTGCT | 10055 |
| rs774652654 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47131265 | CTGAAGGGGGCGTTG[C/G]GGAGTCCTGAGAGAG | 10055 |
| rs774662296 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47154391 | GCCTGGCTTCTTTGG[G/T]TATATTATAAAGAAG | 10055 |
| rs774667016 | snp | A/G | 1.648e-05 | 0.0028705 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47152920 | TGACTTGCTGCTCCA[A/G]GGATGTCATAGTTAA | 10055 |
| rs774710646 | in-del | -/ATGGTCAAAAAGGTATGTGT | 6.58989e-05 | 0.00573978 | frameshift-variant, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47155201 | TCTTCTGAGACAACG[-/ATGGTCAAAAAGGTATGTGT]ATGGTCAAAAAGGTA | 10055 |
| rs774718262 | in-del | -/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47174075 | AGACGTGAGCCACTT[-/C]GCCCAGCCTGTTTAC | 10055 |
| rs774742478 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47145252 | GTGATCCTCCCACCT[C/T]GGCCTCCCAAAGTGC | 10055 |
| rs774823948 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47169390 | ATCTGGGACTACAGG[C/T]GGCCGCCAGCATGCC | 10055 |
| rs774834042 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47133412 | GAGTATTTTTAGTAG[A/G]GACGGGGTTTCACCA | 10055 |
| rs774881561 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47146342 | TAGATCAGTAATTAC[C/T]GTATAAACTATGGTT | 10055 |
| rs774945306 | snp | C/G | 1.64743e-05 | 0.00287 | missense, utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209237 | GGGATTGTGGAGTGC[C/G]TTGGCCCCAAGTGAA | 10055 |
| rs774998535 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47183210 | CGTGAGCCACTGTGC[C/G]TGACCGGTTCACGTA | 10055 |
| rs775017393 | snp | A/G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47160547 | CTACAGATGCCCGCC[A/G/T]CCATGCCCGACTAAT | 10055 |
| rs775068051 | snp | C/G | 1.64844e-05 | 0.00287087 | intron-variant | SAE1 | GRCh38.p7 | 19:47203780 | AATTGTTAACCATGA[C/G]TTTGTATATGTGCTG | 10055 |
| rs775089318 | snp | C/G | 1.6516e-05 | 0.00287362 | missense, utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209270 | CAAGATTTGGCAGCC[C/G]CAGAGATGCCAACTG | 10055 |
| rs775098435 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47195570 | GATGGGTCTAAGTAT[A/G]TGGCTGGCCCTTCTG | 10055 |
| rs775102354 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47187435 | TTTGTAACACTTGAT[A/G]AGAAACAGAACCATC | 10055 |
| rs775125472 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47173081 | TCACCCAGGTAGGAG[A/T]GCAGTGGGGCGATCT | 10055 |
| rs775169573 | snp | A/C | 0.00204214 | 0.0318889 | intron-variant, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47180191 | ATGCCCAGAGACATC[A/C]CAGAAGCACTGAACG | 10055 |
| rs775214516 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47152603 | TGAGAACTATGAAAT[A/G]TGTATATGTTCGTGG | 10055 |
| rs775397025 | in-del | -/T | 0.00130527 | 0.0255133 | intron-variant | SAE1 | GRCh38.p7 | 19:47153091 | TTCTCCTTTTTATAC[-/T]TTTTTTTTTTAAATT | 10055 |
| rs775443281 | snp | C/T | | | intron-variant, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47180200 | GACATCCCAGAAGCA[C/T]TGAACGCACTCATGC | 10055 |
| rs775464704 | snp | A/G | 1.65652e-05 | 0.0028779 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150220 | ACTCCAGAAGATCCC[A/G]GAGCTCAGTTCTTGA | 10055 |
| rs775505586 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47142924 | GTTTATCTGTCTCCT[A/C]CTTTTTCATGAGGGC | 10055 |
| rs775510014 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47151288 | CCAAGTAGCTAGGAT[A/T]ACAGGCACTCACCAC | 10055 |
| rs775527513 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47166400 | GTTTGTCAAGACAGG[A/G]TAATACAATATACTT | 10055 |
| rs775553786 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47201703 | CAGTGGCACCATCTC[A/G]GCTCACTGCAACCTC | 10055 |
| rs775597858 | in-del | -/TTTTG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184803 | TTTGTTTTGTTTTTG[-/TTTTG]TTTTGTTTTGTTTTG | 10055 |
| rs775598266 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47179899 | GGTTAGCAATTCTGA[A/C]ACTACTTACTGTTCT | 10055 |
| rs775633112 | snp | A/G | 1.64746e-05 | 0.00287002 | intron-variant, synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197336 | TGATGTGCTTGACTC[A/G]CTGGGTATTAGTCCT | 10055 |
| rs775656630 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47169374 | CCTCAGCCTCCCAAG[C/T]ATCTGGGACTACAGG | 10055 |
| rs775681561 | in-del | -/GTGT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167010 | GGCTGGAGTGTAGTG[-/GTGT]GTGTGACCTTGGCTC | 10055 |
| rs775699458 | in-del | -/CTTT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47198686 | CCAGAGTCCCTAGTC[-/CTTT]CTTTGTTGACTTCCT | 10055 |
| rs775706757 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47191872 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTA | 10055 |
| rs775712489 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47185306 | TTTTATTTTTCATTT[C/T]TATTTGTTTACTTAT | 10055 |
| rs775759959 | snp | A/G | 1.64784e-05 | 0.00287035 | intron-variant, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197259 | TTCCGTACAGATAAA[A/G]GAAGAGATCCCAGTT | 10055 |
| rs775770258 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47131371 | AGGGGCTGGGGATAC[A/G]TGGAAAGGGTGAGGT | 10055 |
| rs775799410 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47141605 | AGCCATGATAAAAAA[G/T]CCTTTTTTTGAGGAA | 10055 |
| rs775875985 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47157788 | TGAACAATGCAGGCT[C/T]GGATTCCAACCCCAA | 10055 |
| rs775913293 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47135160 | CACCTTAAGCACTTA[C/T]CCTTTGTGTTACAAA | 10055 |
| rs775950369 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47166932 | CACCTAAACATGACT[A/G]TTTAATCTTCACTAG | 10055 |
| rs775956067 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47207092 | GTTCAAGACTAGCTT[A/G]GGCAACATGAGGAGA | 10055 |
| rs775956902 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47199153 | GCACTTTGGGAGGCC[A/G]AGACAGGCAGATCAT | 10055 |
| rs775985328 | in-del | -/TTTT | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47128827 | TTATTTATTTATTTA[-/TTTT]TTTTTTTCTGAGACG | 10055 |
| rs776003036 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47133496 | TCCCAAAGTGCTGTG[A/T]TTACAGGCGTGAGCC | 10055 |
| rs776039840 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47134105 | TGACCTCGTGATCCA[C/G]CTGCCTCGGCCTCCC | 10055 |
| rs776125283 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47170281 | GCAGTGGGGTGCAAT[A/C]TTGGCTCACTGCAAC | 10055 |
| rs776160931 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47183388 | GAGCCAGAGCTGTCA[C/T]ACTGTCATCCCCAGG | 10055 |
| rs776177770 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47160985 | TGTTAGCTTATCTCT[A/G]TATATATATTTAATT | 10055 |
| rs776182054 | snp | A/G | 1.64936e-05 | 0.00287168 | intron-variant | SAE1 | GRCh38.p7 | 19:47153056 | GTAAGTGTTGGGAGA[A/G]GAGGGGAGAACATAA | 10055 |
| rs776202876 | snp | C/T | 1.65902e-05 | 0.00288008 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209280 | CAGCCCCAGAGATGC[C/T]AACTGCAGCATGCCC | 10055 |
| rs776217644 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47142819 | CTCAGAAAGGCTTGT[A/G]TGATTTCTGTCTCAA | 10055 |
| rs776221582 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47200235 | ACCACGCCCAGCCTC[-/T]TTTTTTTTTTTTTTT | 10055 |
| rs776299854 | in-del | -/C | 0.000214163 | 0.0103458 | intron-variant | SAE1 | GRCh38.p7 | 19:47169811 | AGTTCTGCCTTTTTT[-/C]CCACAGAAGGTGGTC | 10055 |
| rs776307531 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47139139 | GTATTTTGAGTAGAG[A/G]TGGAGTTTCACCATA | 10055 |
| rs776320221 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47198016 | CACTTGGACACTCCA[C/T]GCTTTCACCTTACGT | 10055 |
| rs776338006 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47175022 | CAGTGAGAACATTTA[C/T]AATCACATATTGTGT | 10055 |
| rs776361254 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47139233 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT | 10055 |
| rs776377172 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47176165 | TTGATGGCGTAAATG[A/G]TAGGGGAAGAGCATA | 10055 |
| rs776414683 | in-del | -/TG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137710 | TCAGCTGATTGTGTG[-/TG]TGTGTGTGTGTGTGT | 10055 |
| rs776462504 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47200810 | AATAGTTATAACAAA[C/G]ACCATATGGCCCATA | 10055 |
| rs776596780 | snp | C/G | 6.61332e-05 | 0.00574998 | intron-variant | SAE1 | GRCh38.p7 | 19:47143633 | GAGCTCATTCCTCCC[C/G]TGCTCTGGCTCCCCT | 10055 |
| rs776648218 | snp | A/T | 8.28397e-05 | 0.00643529 | intron-variant | SAE1 | GRCh38.p7 | 19:47197225 | TGCCTTCTTTTTCTT[A/T]TTCCCAGTGCTCTTA | 10055 |
| rs776651308 | snp | C/T | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129514 | TGGCCGGGCTGGTCT[C/T]GAACTCCTGACTTCG | 10055 |
| rs776654173 | snp | C/G/T | 4.942e-05 | 0.00497071 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SAE1 | GRCh38.p7 | 19:47143560 | AATTGCCAAGAATCT[C/G/T]ATCTTGGCAGGAGTG | 10055 |
| rs776663735 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47152692 | GCTGCAGAACGTGAC[A/G]GTCTCATAACTTATA | 10055 |
| rs776673988 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47174035 | GTGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC | 10055 |
| rs776717662 | in-del | -/AAGAA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47193848 | AAAAAAAAGAAAGAA[-/AAGAA]AAAGAAAAAGAAATT | 10055 |
| rs776723360 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47205761 | TACTCATTTCATCTC[A/C]CACCGGCCCTATGAG | 10055 |
| rs776725055 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47187471 | TAGCTTGAACACTTT[C/T]CAATTCAGTCAGTAA | 10055 |
| rs776738228 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47181477 | TGTTTTTTCTTTTCC[-/T]TTTTTTTTTTTTTTT | 10055 |
| rs776774381 | snp | A/G | 0.000187882 | 0.00969049 | intron-variant, synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47180291 | TTCCAGATCTGGGGT[A/G]GGAAAATTACAGGTG | 10055 |
| rs776843307 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47180039 | AGCCATGTGGTATTG[A/G]ATTGGAATTGAAGTT | 10055 |
| rs776858129 | in-del | -/TTTT/TTTTT | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129817 | TCCTTTCTTTCTTTC[-/TTTT/TTTTT]TTTCTTTTTTTTTTT | 10055 |
| rs776888566 | in-del | -/AGAAAG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47193840 | CAAAAAAAAAAAAAA[-/AGAAAG]AAAAGAAAAAGAAAA | 10055 |
| rs776939871 | in-del | -/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47148030 | CTCCCAAAGTGCTGG[-/G]ATTACAGGCGTGAGC | 10055 |
| rs776982062 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47192421 | GCCCAGCTAATTTTT[A/G]TATTTTTAATAGAGA | 10055 |
| rs777006357 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47193982 | AAGCATAGCCCAGAA[G/T]CAGGGTGTGTCTTTT | 10055 |
| rs777009520 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47171554 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 10055 |
| rs777019959 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47144015 | CATTTAGGTCTGAGG[C/T]GAGCTCAGGAGTATG | 10055 |
| rs777043781 | snp | A/G | 8.28246e-05 | 0.00643471 | intron-variant | SAE1 | GRCh38.p7 | 19:47155252 | GTCAGAAACCCTGGG[A/G]CCTTGGAGGGGTCAG | 10055 |
| rs777167701 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47210069 | ACTCAGAGGCTGTTG[A/C]ATTTCAGGGCTATGT | 10055 |
| rs777179489 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47143067 | GCCTGTCTCTTTCCT[A/G]GATTCGAGGTGTGAT | 10055 |
| rs777217967 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47150958 | TTTCACTGCCAAATC[C/T]ATGCGGAGGTGAAAG | 10055 |
| rs777317139 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47151682 | TTTGTCCTGTTTTCT[A/T]TTTCCTAGTCCCTTC | 10055 |
| rs777328105 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47206496 | TTTTGCGTCTTTCCT[G/T]TCTTACGTCCTTCTA | 10055 |
| rs777376752 | in-del | -/TTTC | | | intron-variant | SAE1 | GRCh38.p7 | 19:47151467 | TTTTTTACACTTTTC[-/TTTC]TTTCTTTCTTTCTTT | 10055 |
| rs777387596 | snp | G/T | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190321 | TGGTGGGAGGTGCTC[G/T]TCAGAAATGCAGTCA | 10055 |
| rs777496153 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167447 | GAGTTTCGCCATGTT[A/G]GCCAGGATGGTCTCG | 10055 |
| rs777514593 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47166083 | CTCCTGCCCAGACAA[C/T]CCCAAGCTTCTCAGG | 10055 |
| rs777562690 | snp | C/T | 0.000133643 | 0.00817335 | intron-variant | SAE1 | GRCh38.p7 | 19:47197427 | CAGATAAAGTTTGTT[C/T]TCAGGATTTGCCTTA | 10055 |
| rs777577574 | snp | A/G | 1.68286e-05 | 0.0029007 | intron-variant | SAE1 | GRCh38.p7 | 19:47150404 | TATAAAATCTGCTGT[A/G]GGAATTAAACAAATT | 10055 |
| rs777585187 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47207774 | TGAGGCACTGAGACT[A/G]TAAGCACACGCCACC | 10055 |
| rs777587043 | in-del | -/ATTTA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47140844 | TGATGGCAGTTGAGT[-/ATTTA]ATTTAATTTAATTTA | 10055 |
| rs777596386 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47179346 | CCCTGTCTCTACTAA[A/G]GTACAAAAAAATTAG | 10055 |
| rs777601112 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47142276 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 10055 |
| rs777617391 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47157336 | ATAGCTCCGTGAATT[G/T]GGTGGGGGGAGATAA | 10055 |
| rs777628844 | snp | A/T | 4.94189e-05 | 0.00497062 | intron-variant, missense, synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47203695 | CTCCGAGATGGCCCC[A/T]GTGTGTGCGGTGGTT | 10055 |
| rs777637382 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47177864 | TTGCAGAGCAACACA[C/T]GCACAGGGCCAGCAG | 10055 |
| rs777650370 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47165636 | CCTGAAGGCATTGTC[A/G]GGTGTATTTTTTCTT | 10055 |
| rs777696136 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47136073 | CATTTGTCTGTTGAT[-/A]AGACATATGGGTTGC | 10055 |
| rs777740912 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47161265 | ATCCTCTTGCCTTGG[A/C]CTCTCAAAGTGCTGA | 10055 |
| rs777758915 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47185627 | GTTTTTTTGAGACAG[A/T]GTCTCACTGTGTCTC | 10055 |
| rs777780546 | in-del | -/T | 3.69573e-05 | 0.00429852 | intron-variant | SAE1 | GRCh38.p7 | 19:47150184 | CAAGACTTAAAAAAA[-/T]ATGTGTATTATTCCT | 10055 |
| rs777782267 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47139346 | CGCGCCTGGCACACC[C/T]AGCTAATTTTTTTTT | 10055 |
| rs777782653 | in-del | -/TGTATTTT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47201542 | CGCCCAGCTAATTTC[-/TGTATTTT]TGTATTTTTAGTAGA | 10055 |
| rs777840776 | snp | A/G | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47153016 | GATACACATTTGCCA[A/G]TCTAGGAGAGCATGA | 10055 |
| rs777842304 | in-del | -/TCC | | | intron-variant | SAE1 | GRCh38.p7 | 19:47194109 | GCTTCTAAAACTGTG[-/TCC]TCCTCAGTTGTTCTC | 10055 |
| rs777917610 | snp | A/T | 1.65091e-05 | 0.00287303 | intron-variant | SAE1 | GRCh38.p7 | 19:47155090 | TAGGGTAAAATTACA[A/T]TCTCTCCCCTTGTCA | 10055 |
| rs777952518 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47170056 | TAGTTCTCAGTGATC[A/C]CTTGAGAAAGGGGTG | 10055 |
| rs778028357 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47133143 | GCAGGAACCAAATGA[C/T]TTGAGGAGTAGCTTT | 10055 |
| rs778038466 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184557 | CTGGGATGACAGGCA[C/T]CCGCCACCATGCCCA | 10055 |
| rs778044737 | snp | A/C | 2.43727e-05 | 0.00349081 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209356 | AGGAAAACTGAAGTC[A/C]TTGGCCCGATACAAA | 10055 |
| rs778064307 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47162000 | ATTAATTAAAATCAA[A/G]TCAAATCAAATATTT | 10055 |
| rs778098456 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47133063 | AGAACTTTCCTAGCT[A/G]AGAGAACAGCAAGTG | 10055 |
| rs778118040 | in-del | -/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167745 | TGAAATTATTTGCAT[-/C]CCCCCCCACCGCCCA | 10055 |
| rs778127148 | snp | A/C | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47143597 | CTGACCATGCTGGAT[A/C]ACGAACAGGTGCGCT | 10055 |
| rs778173452 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163466 | GGCGCAGTGCCTCAC[A/G]CCTGAAATCCCAGCA | 10055 |
| rs778247455 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47145400 | GATCCGCTGGCCTCG[G/T]CCTCCCAAAGTGCGG | 10055 |
| rs778278825 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47173667 | TGCCAGTAATATCTC[C/G]CCACCCAGCTCTAAC | 10055 |
| rs778288624 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47189785 | GACAGTGACTTTATT[G/T]TCTTCCTACTAAAGT | 10055 |
| rs778293338 | snp | A/G | 1.68012e-05 | 0.00289833 | intron-variant | SAE1 | GRCh38.p7 | 19:47197199 | AAAAAAAAAAAAGTG[A/G]CTTTATAACCTGCCT | 10055 |
| rs778336657 | snp | A/C/T | 4.94192e-05 | 0.00497067 | synonymous-codon, missense, nc-transcript-variant, utr-variant-5-prime | SAE1 | GRCh38.p7 | 19:47143507 | AGGCTGCGGGCCTCT[A/C/T]GGGTGCTTCTTGTCG | 10055 |
| rs778378584 | in-del | -/TG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47161037 | GATGGGATGTAACTC[-/TG]TAGCCCAGGCTGGAG | 10055 |
| rs778424084 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47205416 | CTATGTAATGGGCAC[C/T]GAGGAGATATTTGGA | 10055 |
| rs778451445 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47138946 | TCTAAGGAGGTGACA[A/G]TTGAGCTGAGACCTA | 10055 |
| rs778522898 | in-del | -/TTT | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129299 | GGTGGGCATGGTGGC[-/TTT]TTTTTTTTTTTTTTT | 10055 |
| rs778526435 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47136441 | CCACACCCAGCCTGA[G/T]TTATTTTCATTTGGG | 10055 |
| rs778537216 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47206372 | CAGGCGGGGCCTGCA[A/G]TCCAAGGGCCTCAGA | 10055 |
| rs778616741 | snp | C/T | 1.66065e-05 | 0.00288149 | intron-variant | SAE1 | GRCh38.p7 | 19:47169958 | CTTACCCCGGGAGAG[C/T]TTTTGGCTCTGATTT | 10055 |
| rs778623626 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47153326 | ATTCAACCAAAGTCT[A/G]CCTTGGAAAAGGTGT | 10055 |
| rs778639976 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47168178 | GCCTGGGTGACAGAG[A/G]GGGAGACTGTCTGGA | 10055 |
| rs778712319 | snp | C/T | 1.70035e-05 | 0.00291572 | | | GRCh38.p7 | 19:47150418 | TGGGAATTAAACAAA[C/T]TAAGGTGCTAGTTGT | 10055 |
| rs778722889 | snp | A/G | | | | | GRCh38.p7 | 19:47192966 | TTATTTACTACAATC[A/G]GAATACCAGCAGGAC | 10055 |
| rs778739201 | in-del | -/T | 0.000472813 | 0.0153682 | | | GRCh38.p7 | 19:47131088 | GTCTATTCTGAGGCG[-/T]TTGCGGCCCGGAAGG | 10055 |
| rs778779125 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47143908 | AGAAGTGTTTTTCCA[A/G]TTTGTGCCTAAAAAT | 10055 |
| rs778780328 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47144745 | AAACAACACTGGATC[A/G]GAGAGAATGTGGGCA | 10055 |
| rs778811157 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47181021 | GATGTTAGTGGAACA[A/G]TTGGTAAAAAGAGGC | 10055 |
| rs778818576 | snp | A/G | 6.44268e-05 | 0.00567532 | utr-variant-5-prime, nc-transcript-variant, missense, intron-variant | SAE1 | GRCh38.p7 | 19:47130899 | CGGTTGGCTTGAGCG[A/G]GACCGGAGCTGAGGC | 10055 |
| rs778826578 | snp | A/G | | | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210972 | CCCTGTACCTCTAAC[A/G]GCAGAGATTAAGTCA | 10055 |
| rs778873170 | snp | A/G | 1.64735e-05 | 0.00286993 | intron-variant, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47203727 | GAGGGATTTTGGCAC[A/G]GGAAATTGTGAAGGT | 10055 |
| rs778894891 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47189897 | TAATAATGTTGCTGT[A/C]CAGATTCCCGTTATA | 10055 |
| rs778904515 | in-del | -/TTTT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184809 | TTTGTTTTTGTTTTG[-/TTTT]GTTTTGTTTTGTTTT | 10055 |
| rs778913288 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47196045 | TGCCTCTTCCGGGTC[-/T]TTTTTTTTTTTTTTT | 10055 |
| rs778916505 | snp | C/T | 0.000335186 | 0.0129414 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209368 | GTCATTGGCCCGATA[C/T]AAAACATTTCCTGCA | 10055 |
| rs778920898 | in-del | -/GAGAGGCTCG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47131569 | TCAAATGGGAATCTT[-/GAGAGGCTCG]GAGAGGCTGGAGGGG | 10055 |
| rs779112867 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47134709 | GGGCAAAGTTGGTGA[A/G]GTTTAAACTGGAATG | 10055 |
| rs779159454 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47136032 | TGGTCTCAATCTCCT[A/G]ACCTCGTGTACCACA | 10055 |
| rs779220625 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47186807 | GGACTTTTGGAGCAC[A/C]AAAAGGGGCATTTCA | 10055 |
| rs779229469 | snp | C/G | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150330 | GAAGGTGGACACTGA[C/G]GATATAGAGAAGAAA | 10055 |
| rs779235444 | in-del | -/GAAAA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47193845 | AAAAAAAAAAAGAAA[-/GAAAA]GAAAAAGAAAAAGAA | 10055 |
| rs779254948 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47164454 | TTACAGGCATGAGCC[A/C]CCACGTCTGGCCTGG | 10055 |
| rs779312324 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47185952 | ACTCAAAAAAATGCT[C/T]ATTGGCCCCGGGCGT | 10055 |
| rs779323679 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163712 | AGCCTGGGCGACAGA[A/G]CAAGACTCTATCTCA | 10055 |
| rs779328687 | snp | C/T | 1.64857e-05 | 0.00287099 | intron-variant | SAE1 | GRCh38.p7 | 19:47155106 | TCTCTCCCCTTGTCA[C/T]CCTCTAGGGAGAAAA | 10055 |
| rs779344924 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47162374 | ACCTGGGAGTAAAAT[C/T]AAGATAAGGGCATTT | 10055 |
| rs779388841 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47150183 | ACAAGACTTAAAAAA[A/T]TATGTGTATTATTCC | 10055 |
| rs779402836 | in-del | -/TT | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129300 | GTGGGCATGGTGGCT[-/TT]TTTTTTTTTTTTTTT | 10055 |
| rs779418910 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47162127 | CATCACAGCTAGTTC[C/T]CTTGGACAGCCCTGC | 10055 |
| rs779428621 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47147080 | GATGGAAGCTTGGGG[-/A]CAGCCACACCTAAGA | 10055 |
| rs779433731 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47202035 | GGTCCTGGCCAGGGC[A/G]TAAGGAGCCGGAGGT | 10055 |
| rs779456252 | snp | A/G | 0.000106949 | 0.00731184 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209364 | TGAAGTCATTGGCCC[A/G]ATACAAAACATTTCC | 10055 |
| rs779469484 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47175800 | TCAGATCTGGAGTTC[C/T]GTGAGTTAGGGAAAC | 10055 |
| rs779472626 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184696 | GATTACAGGCGTGAG[C/T]CACCACTGCCGGCCT | 10055 |
| rs779497858 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47177042 | TAGAGCAGGAAGAAA[C/T]GGACTTCATCTCAAG | 10055 |
| rs779506724 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47154931 | ACAATAATTTCCTGA[C/G]TGCCCAACAGTGTAC | 10055 |
| rs779560891 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47198937 | ACAAAAAATAGAAAA[A/G]TTAACTGGGCATCGA | 10055 |
| rs779561593 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47189997 | TTGTATATTCACATA[G/T]CCACAGTTTTTTCTA | 10055 |
| rs779622165 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47179165 | CCACTGCACTCCAGC[A/G]TGGGCGACAGAACAA | 10055 |
| rs779630993 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47154289 | AGAGACGGGGTTTCA[C/G]TATGTTGGCTATGCT | 10055 |
| rs779771552 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47140924 | CACAGTCTTGGCTCA[C/T]TGAAACCTCTGCCTC | 10055 |
| rs779794688 | snp | C/T | 1.66402e-05 | 0.00288441 | intron-variant | SAE1 | GRCh38.p7 | 19:47197213 | GGCTTTATAACCTGC[C/T]TTCTTTTTCTTATTC | 10055 |
| rs779795463 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167560 | TTTGAACTTTTATCT[C/G]TCAAATCTATATGCA | 10055 |
| rs779807971 | in-del | -/CT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47192045 | GGCAACAGAGCGAGA[-/CT]CTGTCTCAAAAAAAA | 10055 |
| rs779810446 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47139098 | CTGGGACTACAGGCA[C/T]GTGCCACCACGCCTG | 10055 |
| rs779839088 | snp | A/G/T | 3.29469e-05 | 0.00405864 | intron-variant, synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197297 | ATATGAGGAAGATTC[A/G/T]GAGTTGTTGCTCCAG | 10055 |
| rs779853907 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47205477 | TCTTTCCTTGCTCAC[A/G]TTTTATACATAGCCC | 10055 |
| rs779857571 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47206420 | AGGCACTGTCTGAGC[A/G]CCTATGGAAAGCTTA | 10055 |
| rs779874634 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47153690 | CCAAGTTTCTTGCCT[A/G]TAAAATCAAGATGGG | 10055 |
| rs779913394 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47132622 | CGCAGTGACTCACAC[C/T]TGTAATCCCAGCACT | 10055 |
| rs779953556 | snp | G/T | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129890 | GGCATGATCTTGGCT[G/T]ACTACAACCTCCGCC | 10055 |
| rs779959393 | snp | A/G | 3.30852e-05 | 0.00406712 | intron-variant | SAE1 | GRCh38.p7 | 19:47155067 | TTTGATTCCAATAAC[A/G]TGATTCCTAGGGTAA | 10055 |
| rs779979289 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47144843 | TTTGTTTGTTTGTGT[G/T]TTTTTGCGAGACGAG | 10055 |
| rs779999980 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47196824 | GCTGTCACAGCACTT[C/T]TCACAGTAAGGTAAA | 10055 |
| rs780000036 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47181312 | CAAGAGCGAAACTCT[A/C]TCTCAAAATAGTAAT | 10055 |
| rs780012607 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47153002 | TTTTGGCTACCATGG[A/G]TACACATTTGCCAAT | 10055 |
| rs780153840 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209780 | CCTTAGAGAGGAAAA[A/C]CATGACAGGCAAATG | 10055 |
| rs780154651 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47132355 | CAAGGCTCAAGGGAT[A/G]TTCCCTCTTCAGCCT | 10055 |
| rs780165342 | in-del | -/CAT | 1.64765e-05 | 0.00287019 | intron-variant | SAE1 | GRCh38.p7 | 19:47203747 | ATTGTGAAGGTAAAA[-/CAT]CACTGTGGAGCAGAA | 10055 |
| rs780268439 | in-del | -/TTTCT/TTTT | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129821 | TTCTTTCTTTCTTTC[-/TTTCT/TTTT]TTTTTTTTTTTTTTT | 10055 |
| rs780289741 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47196880 | TCTCTGACTATGTTT[A/G]TTGAATAAATAAAAA | 10055 |
| rs780322904 | snp | A/G | | | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47211104 | ATCATAAAAATGAAG[A/G]AAAAAAGGCCAGGCG | 10055 |
| rs780348591 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47159413 | CCATTTTAAGCTCCA[C/T]AGGGGGAAGGTAGTC | 10055 |
| rs780366964 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47158433 | GTCACAATCAGGTCT[C/T]GGGCACAAGCCTCAC | 10055 |
| rs780402115 | snp | C/T | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47176351 | GACTAATGTGACTGA[C/T]GATGCCTTAGGAATT | 10055 |
| rs780418711 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47202280 | TTTGGGTTTAAAATT[A/C]TACCTATTTATTTAT | 10055 |
| rs780420998 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47199792 | ACTTGCTTCTCACAA[A/G]CTGGTCATTCCTCCA | 10055 |
| rs780472841 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47150582 | GTCTGTTGCATCTGC[C/T]GTAGTTGTTGGTGAC | 10055 |
| rs780493935 | snp | A/C | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190459 | CTGCCTGTCAAGAAC[A/C]TGGCTTTCTTCCTGC | 10055 |
| rs780524600 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47139756 | ACCACTCCCGGCCAA[-/T]TTTTTTTTTTTTTTT | 10055 |
| rs780595964 | snp | A/G | 1.64993e-05 | 0.00287218 | intron-variant | SAE1 | GRCh38.p7 | 19:47155228 | GGTATGTGTAACGTG[A/G]GGGCAGAGGTCAGAA | 10055 |
| rs780606960 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47164026 | CGCCCACATCGGCCT[C/T]CCAAAGTTTTGGGAT | 10055 |
| rs780617260 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47201010 | TTACGGGCATACGCC[A/C]CCATGCCCAGCTATT | 10055 |
| rs780635664 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47165811 | AGAAGCACTGAATAA[C/G]TACTGTTATCTGAGA | 10055 |
| rs780636392 | in-del | -/CTTGTGTTT | | | cds-indel, nc-transcript-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210573 | TTCACCCCACTCTTG[-/CTTGTGTTT]CTTCTTTATGTAAAT | 10055 |
| rs780639055 | in-del | -/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182214 | TTTGGTGATTAGTTC[-/G]TCTTCAGAAGAAACT | 10055 |
| rs780641058 | in-del | -/AAAGACGGGATTTCACC | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129999 | TTTTTTATTTTTACT[-/AAAGACGGGATTTCACC]AAAGACGGGATTTCA | 10055 |
| rs780670101 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47142111 | AAACAAGGCTGGGCA[C/T]GGTGGCTCATGCCTG | 10055 |
| rs780694570 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47177197 | CAAACATTTTGTGAG[C/T]ACCTGCTATGTACCA | 10055 |
| rs780717255 | in-del | -/ACTGTGGAGGGCCTGGTC | | | intron-variant | SAE1 | GRCh38.p7 | 19:47188889 | GAGGTGGTTCTGCCA[-/ACTGTGGAGGGCCTGGTC]ACTTGACAAGGCACC | 10055 |
| rs780729381 | in-del | -/TTTTTT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47201375 | TTTTTTTTTTTTTTT[-/TTTTTT]TTTTTTTTTTTTTTG | 10055 |
| rs780780799 | in-del | -/CTGT | | | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209567 | CTTATGCTGTCCCGG[-/CTGT]CCTCGCCAGCCCTCT | 10055 |
| rs780825201 | in-del | -/C | 1.64779e-05 | 0.00287031 | intron-variant | SAE1 | GRCh38.p7 | 19:47203643 | TCTGTTCCCAGTGCT[-/C]CATTTTCCTTGTCTT | 10055 |
| rs780984128 | snp | C/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150289 | TCTTTGGAGCGAGCT[C/G]AGAATCTCAACCCCA | 10055 |
| rs781019960 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47141010 | CCCGCCACCAACATG[A/C]CCAGCTAATTTTTTT | 10055 |
| rs781037462 | snp | C/T | 1.69499e-05 | 0.00291112 | intron-variant | SAE1 | GRCh38.p7 | 19:47150199 | TATGTGTATTATTCC[C/T]AGGTAACTCCAGAAG | 10055 |
| rs781037567 | snp | A/G | 1.67483e-05 | 0.00289377 | intron-variant | SAE1 | GRCh38.p7 | 19:47197415 | GTTTAGTCTGGACAG[A/G]TAAAGTTTGTTTTCA | 10055 |
| rs781064101 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47161520 | TGGTACATTTGTGTG[A/G]ATTAAAAAAGACACC | 10055 |
| rs781082490 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47207478 | TGTCTTCCTCTTTAA[A/G]TGGTAGCTTGTGGTG | 10055 |
| rs781137133 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184262 | GTTTCTTCTCTTTTC[C/T]AAAGGTGACACTATA | 10055 |
| rs781141187 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47168665 | TGGAGTGCAATGGCG[C/T]GATCTCAGCTCACTG | 10055 |
| rs781153066 | snp | C/T | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129699 | TTTTTGTATTTTTAA[C/T]AGAGATAGCGTTTCC | 10055 |
| rs781205345 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47195898 | CCATACTTGGCTAAA[-/T]TTTTTTTTTTTTTTT | 10055 |
| rs781214118 | snp | A/G | 1.64765e-05 | 0.00287019 | intron-variant | SAE1 | GRCh38.p7 | 19:47203745 | AAATTGTGAAGGTAA[A/G]ACATCACTGTGGAGC | 10055 |
| rs781235835 | in-del | -/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47133397 | CACCCGGCTAATCTT[-/G]AGTATTTTTAGTAGA | 10055 |
| rs781266466 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47199105 | ATACATATAGCGTAA[A/G]GCTGGGCGCGGTGGC | 10055 |
| rs781296175 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182657 | GCCTTACAGCAGAGA[A/G]CTCATGAGAGAACAG | 10055 |
| rs781296446 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47159622 | TGCAGTGGTTCAAAC[A/G]CTGCTCACTGCAGCC | 10055 |
| rs781359109 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, utr-variant-3-prime, synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209206 | CTTCTTCTTCTTCGA[C/T]GGCATGAAGGGGAAT | 10055 |
| rs781410143 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47194423 | TCCTGGTAGAGAGTA[-/T]TAATTTGCTGAATAA | 10055 |
| rs781411028 | snp | C/G/T | 9.94158e-05 | 0.00704975 | intron-variant | SAE1 | GRCh38.p7 | 19:47169950 | AAGCACAACTTACCC[C/G/T]GGGAGAGCTTTTGGC | 10055 |
| rs781432657 | in-del | -/C | 1.64754e-05 | 0.00287009 | frameshift-variant, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47153013 | ATGGATACACATTTG[-/C]CAATCTAGGAGAGCA | 10055 |
| rs781453786 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47173522 | AATACTCTGGAAACT[A/G]CAGAGGATAAAATCA | 10055 |
| rs781481151 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47146234 | CTAGGAAGCCCCACT[A/G]TAAGCTTTTACTTAA | 10055 |
| rs781494553 | in-del | -/AAAGA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47193847 | AAAAAAAAAGAAAGA[-/AAAGA]AAAAGAAAAAGAAAT | 10055 |
| rs781498775 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47165906 | TAGAGCATTGTCATT[-/A]ATGTGTATCTGCATC | 10055 |
| rs781619799 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47169274 | TTTTTGAGGAGTCTT[-/A]ACTCCTTCATCCAGA | 10055 |
| rs781651378 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167931 | GGCACAGTGGCTCAC[A/G]CCTATAATCCCAACA | 10055 |
| rs781691113 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47196511 | TGGGACTACAGGCAC[A/G]TGTCACCACACCTGG | 10055 |
| rs781694883 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137605 | CGGGTTCAAGGGATT[A/C]TCCCGCCTCAGCCCC | 10055 |
| rs781713465 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47169848 | CCTGTTAAAGAAGCC[C/T]TGGAGGTGGACTGGA | 10055 |
| rs781723957 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47187219 | AGTGGCTTCCGTGAA[A/G]TGTCCCTACCTCCTC | 10055 |
| rs796066619 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47149660 | TTTTTTTGTTGACAG[A/T]GAATTTTCTTTATAA | 10055 |
| rs796067782 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47138707 | AAGTAGTGTAGCTTA[A/G]CACAGTGGTGTGTGG | 10055 |
| rs796120464 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47195055 | CACACCTGGCCAGTC[-/T]TTTTTTTTTTTTTTT | 10055 |
| rs796152171 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47142092 | TACAGATTTAAAAAG[C/T]TAAAAACAAGGCTGG | 10055 |
| rs796161659 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47178762 | TAGGCATGAGCCATC[A/G]TGCATAGCCTGCGTT | 10055 |
| rs796205584 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47151138 | ATTTGGGTTGGGTAG[-/T]TTTTTTTTTTTTGCA | 10055 |
| rs796211422 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47195755 | TTTTTTTTTTTTTTT[-/T]GACAGGGTCTCACTC | 10055 |
| rs796389521 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47136037 | TCAATCTCCTGACCT[C/T]GTGTACCACAATTTC | 10055 |
| rs796392383 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47156045 | GCCCGACCAGAAAAC[-/T]TTTTTTTTTTAAAGC | 10055 |
| rs796400988 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47157907 | CTGCGGACCGACTGG[A/G]CTGGACTGGGTTTTG | 10055 |
| rs796451643 | in-del | -/GTGTGTGT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182465 | AAAGAAAAAAGCGTA[-/GTGTGTGT]GTGTGTGTGTGTGTG | 10055 |
| rs796465654 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47164474 | GTCTGGCCTGGAGCG[C/T]GTGATTTTAAATGTC | 10055 |
| rs796481411 | in-del | -/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47178212 | CGCGCCACTGCACTC[-/C]AGCCTGACGACAGGG | 10055 |
| rs796529815 | in-del | -/TT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47196045 | TGCCTCTTCCGGGTC[-/TT]TTTTTTTTTTTTTTT | 10055 |
| rs796614597 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47136495 | ATTTTTACCCGAGTC[-/T]TTTTTTTTTTTTTTT | 10055 |
| rs796695566 | in-del | -/A | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130383 | AAAAAAAAAAAAAAA[-/A]TTGACAGTTCAATGT | 10055 |
| rs796774317 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182355 | GAGAAAGAGACAGCC[A/C]CAGGGAAATGGGTTC | 10055 |
| rs796781113 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47140645 | AAAAAAAAACCCATA[A/C]ATCAGCCAGGTGCAG | 10055 |
| rs796872556 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47206116 | TAGTTTCTCACATCC[C/G]CATCCTCACACAGCC | 10055 |
| rs796877071 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163665 | TTGGGAGGCAGAGGT[C/T]GCAGTGAGCCAAGAT | 10055 |
| rs796884754 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47142620 | ATTGCATGTAAGAGC[C/T]TTCATGATGTGGCCC | 10055 |
| rs796932098 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47203056 | TGGCAGAGCACACTT[C/T]CTTTGGGGAAGTGGT | 10055 |
| rs796942231 | in-del | -/TCCT | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129794 | CTCTCTTTCCCTCCC[-/TCCT]TCCTTCCTTCCTTTC | 10055 |
| rs796976420 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47156348 | CTGGGCAAGGTGGTG[C/T]GTTGCTTGTAGTCCC | 10055 |