SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs145694990 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169403 | GAGATTTCATCCATT[G/T]CTGAGGCTATAGAGA | 5663 |
rs145710546 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73162017 | AAAAAAAAAAAAAAA[A/T]AGAAAAAGAAACCAA | 5663 |
rs145727060 | snp | A/T | 0.0283406 | 0.115616 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193199 | CCTGTAGTTCCAGCT[A/T]CTTAGGAGGCTGAGG | 5663 |
rs145786784 | in-del | -/A | | | | | GRCh38.p7 | 14:73194269 | TTGTTTTTTTCTTCC[-/A]AAGACAGGATCTCTC | 5663 |
rs145840421 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157338 | CAGATGGGGTTTCAC[C/T]GTGTTGGCCAGGCTG | 5663 |
rs145930265 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148885 | TTACAGTGAGCTGAC[A/G]TCGCGCCATTGCACT | 5663 |
rs145930949 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73218628 | CGGAGGAGCCTGTGC[A/G]GGAAGAATGCTCCCA | 5663 |
rs145949063 | snp | A/G/T | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145360 | GTTTTTTTGAGACAG[A/G/T]GTCTCACTCTGTCAC | 5663 |
rs145949376 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PSEN1 | GRCh38.p7 | 14:73213299 | GAGGAAATAACATAA[C/T]AGTTGTTGACCAGAG | 5663 |
rs146071629 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73217229 | AACCATAGCCTGTTT[C/T]GTAGCCATATTAATT | 5663 |
rs146072458 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200296 | TGTGTGTGTGAGACA[A/G]TCTCTCTCTGTCACC | 5663 |
rs146172047 | snp | C/G | 0.0356815 | 0.128715 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186235 | AAATACAGAATTAGC[C/G]AGGTGTGGTGGCACA | 5663 |
rs146190421 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179789 | TCAGCTCACTGCTAG[C/T]ACTTCTAATTCCCCA | 5663 |
rs146191854 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167743 | AAATAACGTTTTCTG[-/T]TTTTTTTTTTGTCTT | 5663 |
rs146224505 | in-del | -/G | 0.0345262 | 0.126772 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216068 | CCATCAACTGGTAAA[-/G]TGGATAAGCAAACCA | 5663 |
rs146269771 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219553 | TTGAGGGACGAGGTC[A/G]AGGAGATATGATAGG | 5663 |
rs146306647 | snp | A/G | 0.00158053 | 0.0280672 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217272 | TAATAAGAATGTGTC[A/G]GAGCTCTTAATGTCA | 5663 |
rs146323073 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73147454 | TGCAAAATTAAAAGC[A/G]CTAGACAAATGATTT | 5663 |
rs146351908 | in-del | -/T | 0.0189856 | 0.0955633 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210437 | GATGAGACCTAATGC[-/T]TTTATCTTCTCTATA | 5663 |
rs146373308 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73141317 | GTGGGATGGAAGGAG[-/A]AAAAAAAAAAATCAC | 5663 |
rs146477595 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139540 | AGCCGAGATCATGCC[A/G]CTGCACTCCAGACTG | 5663 |
rs146516501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210241 | CAGTGGAAAAAAATG[A/G]GGCAGTTTTCCAAAG | 5663 |
rs146592791 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193612 | ACACACAAAATGCTC[A/T]ATTCATTTTTTAAAC | 5663 |
rs146635005 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197144 | TTCACCGTGTTAGCC[A/G]GGATGGTCTTGATCT | 5663 |
rs146648448 | in-del | -/C | | | frameshift-variant | PSEN1 | GRCh38.p7 | 14:73217191 | GTAAAGCCTCAGCAA[-/C]CAGCCAGTGGAGACT | 5663 |
rs146711194 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73214044 | ACAATGGTCATAGTA[A/T]TATTGTTCATAACAG | 5663 |
rs146729897 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210573 | TTTAAGGTAGGAATG[A/C]GTATCAGAAGTGAGG | 5663 |
rs146753793 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73176136 | CCATCTGTATAATCT[A/G]TTAGTAATGTATGGA | 5663 |
rs146833389 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157188 | TGGAGTGCAGTGGCA[C/T]GATCTTGGCTCACTG | 5663 |
rs146833908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200513 | CAACTGCCTCAGACT[C/T]CCAAAGCATTAGTAT | 5663 |
rs146853341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197623 | TAATCTTTTTAATTT[A/G]TAGTTCATATCCGTG | 5663 |
rs146855665 | snp | A/G | 1.64784e-05 | 0.00287035 | missense | PSEN1 | GRCh38.p7 | 14:73170986 | CCTGTGACTCTCTGC[A/G]TGGTGGTGGTCGTGG | 5663 |
rs146875208 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | PSEN1 | GRCh38.p7 | 14:73159486 | CATTAGGTCTGTGAT[C/G]CTTTTGAAGTTGATT | 5663 |
rs146942755 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198413 | TGATTAGGGCAAGCT[A/C]AAGGATTCCTTTGAG | 5663 |
rs147032287 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73183080 | AATTTAGGCTAAAGT[C/T]GAAGTATTTGGAGGG | 5663 |
rs147049211 | snp | A/T | 0.142947 | 0.22592 | intron-variant | PSEN1 | GRCh38.p7 | 14:73178027 | CGGTTCAAGTGATTC[A/T]CCTGCCTCAGCCTCC | 5663 |
rs147183622 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154677 | AAAGGCTTGAAATAT[A/G]TGACAGATATATCCC | 5663 |
rs147183738 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PSEN1 | GRCh38.p7 | 14:73199101 | TGTGAAGGATCTGTT[C/T]AGTTTTATATCTTTC | 5663 |
rs147199304 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195970 | AATATTCTTTTCACC[A/G]TATTACAATATTTTT | 5663 |
rs147219036 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157580 | ATAATGAAAATGTCC[A/G]TTACCTCCAGAAGTT | 5663 |
rs147290166 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73178861 | AGCCAGCCTTGTCAA[A/T]GCCTTTGCAGTGTTG | 5663 |
rs147290304 | snp | A/G/T | 0.00914918 | 0.0670815 | intron-variant | PSEN1 | GRCh38.p7 | 14:73138159 | AACCACAAGGTGATT[A/G/T]TCCCTATTTTAAATT | 5663 |
rs147434149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195361 | TATTTTTAGTAGAGA[C/T]GAGGTTTTGCCATGT | 5663 |
rs147434342 | in-del | -/TACTA | 0.0189856 | 0.0955633 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196384 | TGTGTTTTATTACTG[-/TACTA]TATTATATTATAGTT | 5663 |
rs147502410 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212302 | TTTTAGTAGAGATGG[C/G]GTTTCACCATCTTGG | 5663 |
rs147502524 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73170511 | TTTTCATGCAGGTGT[C/G]AGTATTTAAGGTACA | 5663 |
rs147519551 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73209756 | GAAGTGGTAATAGGG[A/G]ACGGCCCGCTGAAGG | 5663 |
rs147622397 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73150835 | AACACTTTGGGAGGC[C/T]GAGGAGGGCGGATCA | 5663 |
rs147638016 | snp | C/T | 0.000153988 | 0.00877328 | missense | PSEN1 | GRCh38.p7 | 14:73206425 | TGGCAGAAGGAGACC[C/T]GGAAGCTCAAAGGAG | 5663 |
rs147690813 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192267 | ACATGTTGAAACCCT[A/G]TCTGTACAAAAAAAA | 5663 |
rs147691281 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | PSEN1 | GRCh38.p7 | 14:73147104 | TTTTCTCCTGCCTCA[A/G]CCTCCTGAGTAGCTG | 5663 |
rs147759952 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73168474 | TGATTGTCGGAAATA[C/T]AAGCCACTGAGTGTT | 5663 |
rs147796167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171516 | TATATAGAAGGGTGC[A/G]CCCTTACAGATGGAA | 5663 |
rs147813948 | in-del | -/TCTG | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73177520 | TAGTATTATTTGCCC[-/TCTG]TCTGAACATCTTCCT | 5663 |
rs147866042 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73220773 | CCTGCTGCAGTTACC[A/C]TGGAGTTCAGGCTCT | 5663 |
rs147882990 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217725 | GTGAGAGGAGCTGGT[A/G]CCATGCATGACCCCA | 5663 |
rs147903216 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223269 | CTCCCACAGCCTTGG[A/G]CAGCAGGGTGCCTCT | 5663 |
rs147905463 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PSEN1 | GRCh38.p7 | 14:73155732 | TTATGTTGCCCAGGC[C/T]GGTCTTGAACTCCTG | 5663 |
rs148004093 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73218470 | TTGGCCGGGTGAAGA[C/T]TTTCTAGTGTTTCCG | 5663 |
rs148009306 | in-del | -/TACCTTGAGCT | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73147638 | ATTGCTAAAGAGGTC[-/TACCTTGAGCT]TACCTTGAGCTTATA | 5663 |
rs148024075 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73165312 | TTTTTCCTTAAAGAT[C/G]GTGTCTCACTACATT | 5663 |
rs148040036 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204900 | ATAAAAAACTAATCC[A/G]TAAACCTCATACTTG | 5663 |
rs148092059 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73209369 | GAAAAGTAAGAAATA[C/T]ACTGGAAAGAATTGC | 5663 |
rs148143836 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73144587 | ACTCTGTGAATTCCA[A/C]CTCCTCACTTGCCAG | 5663 |
rs148213656 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PSEN1 | GRCh38.p7 | 14:73185659 | AAAACAATTTTTAAG[A/G]TGTATTTCTTTTCTC | 5663 |
rs148219738 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157382 | GACTTCAGATGATCC[A/G]CCTGCCTCGATCTCC | 5663 |
rs148305194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73174035 | TTATATGCATGGAAT[C/T]TATATGTCATGAAAA | 5663 |
rs148356871 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73178964 | TCGGTTGTCAGGGTC[A/G]GTGTGTACTGTTGAG | 5663 |
rs148370307 | in-del | -/C | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136378 | AGGCCGGAGGCCCCG[-/C]CCCCTTCCTCCTGGC | 5663 |
rs148405986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210225 | ATAATATAAAATTCA[C/T]CAGTGGAAAAAAATG | 5663 |
rs148441567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171542 | TGGAACAATGGCAAG[C/T]GCACATTTGGACAAG | 5663 |
rs148475766 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154203 | TATGTATACCTGTGT[G/T]TATATATTGAAAAAC | 5663 |
rs148530636 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158662 | AGATGGAGTCTTCCT[A/G]TGTTTCACAGGCTGA | 5663 |
rs148546614 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200169 | TTGTTTGTCTAATGC[G/T]TTGGGTGATTATTTG | 5663 |
rs148600177 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73150788 | AAAAAAAAAAAAAAA[-/A]GCCAGGTGCGGTGGC | 5663 |
rs148612389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73175930 | AATGAGAGTATCTGT[C/T]GTACCCCACCAGTGC | 5663 |
rs148686567 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PSEN1 | GRCh38.p7 | 14:73190881 | GTTTTTTAGTTTGAG[A/G]ATACTGGAAATGCTT | 5663 |
rs148807303 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73167495 | ACCTTTAATCCATTC[A/G]TGAAGGCAGAGTCCT | 5663 |
rs148841069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160932 | AGGACTTTTTAATGT[A/G]TTCTGGATATTAATC | 5663 |
rs148912177 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204808 | TTGGGAGGCTGAGGC[A/G]GGAGGATTGCTTGAG | 5663 |
rs148914974 | snp | G/T | 0.00953873 | 0.0683987 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135462 | TGATCTCAGCTCACG[G/T]GTTCAAGCGATTCTC | 5663 |
rs148927215 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73177601 | TTTTCTTCCCCTTAG[C/G]ATGTTTTAATTTTAC | 5663 |
rs148929071 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152062 | GACTACAGGCGCCCG[C/T]CACCATGCCTGGCTA | 5663 |
rs148998082 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193390 | TCTCTACTAAAAATA[C/T]AAAAATTAGCTGGGT | 5663 |
rs149088789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181847 | GGCACTGTCTCGGCT[C/T]ACTGCACCCTATACC | 5663 |
rs149119646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168618 | TGGCCTGGCTTCAGG[A/G]AAAGATCACCTTCTT | 5663 |
rs149135830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211685 | CTAGTTACAATGACA[A/G]CTAGTTACTGTTTCC | 5663 |
rs149166990 | in-del | -/AT | 0.0528381 | 0.153711 | intron-variant | PSEN1 | GRCh38.p7 | 14:73164863 | GCTTCTTTTATTTTC[-/AT]ATATATATATATGTT | 5663 |
rs149209990 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156105 | TTTGGAAGGCTGAGG[C/T]GGGTGGATCACTTGA | 5663 |
rs149210266 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73224014 | ATGGATTATAGCACA[C/T]CACAGCTCTGAAGAG | 5663 |
rs149238167 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73206246 | AGAGAACCTTTTTTT[-/T]ATTTTTACTTCTGAT | 5663 |
rs149299753 | snp | A/G | 6.58946e-05 | 0.0057396 | missense | PSEN1 | GRCh38.p7 | 14:73211868 | ATCTAGGGCCTCATC[A/G]CTCTACACCTGAGTC | 5663 |
rs149312199 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195261 | CACTACAACCTCTCC[C/T]TCCCGGGATCAAGCG | 5663 |
rs149385120 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PSEN1 | GRCh38.p7 | 14:73140662 | GTAGGGGCATTATAT[A/G]ACTTCTGGCATTTGC | 5663 |
rs149457419 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73190281 | TCCTTTGAGCCCAGG[G/T]GTTCTAGACCATCCT | 5663 |
rs149562759 | snp | A/G | 1.77998e-05 | 0.00298321 | missense, intron-variant | PSEN1 | GRCh38.p7 | 14:73148099 | TGAGCAATACTGTAC[A/G]TAGCCAGGTACAGTG | 5663 |
rs149577006 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162587 | TTGCTTGAGCCTAGG[A/T]GGTCAACGCTGTGGT | 5663 |
rs149595412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173118 | GGATATGTGACATTA[C/T]CTTAAGACAACTCCA | 5663 |
rs149616406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148253 | CTTCAGCTGATTGCT[A/G]GAGGACACAGGGCTG | 5663 |
rs149643873 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205285 | ATCGAGACCATCCTG[G/T]CTAACACAGTGAAAC | 5663 |
rs149698571 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210002 | AAACTCCTCCATCCT[A/T]GTTATTTCCAAACAC | 5663 |
rs149701354 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | PSEN1 | GRCh38.p7 | 14:73142061 | GACAGAGGGAGACTC[C/T]GTCTCAAAAAAAAAA | 5663 |
rs149750118 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145724 | GAATACATATTGTTT[G/T]TGCATCATACTAAAG | 5663 |
rs149765364 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193167 | ATACAAAAATTAGCC[A/G]GGCATGGTGGTGCAC | 5663 |
rs149873062 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PSEN1 | GRCh38.p7 | 14:73213262 | TTCTACTTTCCTCTT[C/T]TCTCACAGGCACCAG | 5663 |
rs149893475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73164428 | GGCACCTGCTAATAG[C/T]CATAGGAATATGTAT | 5663 |
rs149924956 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219678 | GTTAGGTGAAGTGGT[G/T]TAAACCAAACGGAAC | 5663 |
rs149978366 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PSEN1 | GRCh38.p7 | 14:73155954 | CGGTTTACCACAGTG[A/G]TGCAGGATGTTGATA | 5663 |
rs150046753 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73200722 | GTAGATTTTTTTTGC[C/T]AATTTTTCTGTTGAG | 5663 |
rs150049568 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73166672 | CTTGCTGTCTATCAC[A/G]GTATGTTCTGGTCCC | 5663 |
rs150050804 | snp | G/T | 0.0517044 | 0.152246 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197137 | ACAGGGTTTCACCGT[G/T]TTAGCCAGGATGGTC | 5663 |
rs150079540 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194820 | TGATTCACCTGCCTC[A/G]GCCTCCCAAAGTGTT | 5663 |
rs150124100 | in-del | -/GGTTTT | | | cds-indel | PSEN1 | GRCh38.p7 | 14:73198042 | TAGATTTAGTGGCTG[-/GGTTTT]TTTTGTGTCCGAAAG | 5663 |
rs150191750 | in-del | -/TATAT | 0.0898077 | 0.191933 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196414 | TAGTTCTATATATAC[-/TATAT]TATATTGTACATATA | 5663 |
rs150220443 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73177279 | TGGTTTGTTTTCTCC[C/T]TTGCATATCTCTTCT | 5663 |
rs150235879 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221236 | AATTCATTTTTTTCC[A/G]TGAAATCCCTTCTTC | 5663 |
rs150258982 | in-del | -/TCTA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73158282 | TATTTAACTTTTTTT[-/TCTA]TCTATCTATCTATCT | 5663 |
rs150292692 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157497 | TGACGTAAAATGTAC[A/G]TACTTAAAGTATACA | 5663 |
rs150301281 | snp | A/G/T | 0.000193802 | 0.00984203 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73198053 | GGCTGTTTTGTGTCC[A/G/T]AAAGGTCCACTTCGT | 5663 |
rs150307958 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168513 | AAGTGGCTGAGCAGC[A/G]AGCAGAGAATCAGGT | 5663 |
rs150357761 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201415 | TTATAAAGAAGTCAA[A/T]GGTAATGAGGACTAA | 5663 |
rs150429321 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211227 | GATGTTTTCAAGTAG[A/C]CCAACTTCCTACTCT | 5663 |
rs150435397 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143102 | TTTGCCACGCTGCCT[C/G]AACAGTGGGGTCATT | 5663 |
rs150538359 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179384 | CACTTTGGGAGGCCA[A/C]GGCGGGCAGATTGCC | 5663 |
rs150550252 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222797 | TTATAAAAGTGACTT[A/G]ATTCAGAAATCAATC | 5663 |
rs150562889 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193677 | TTTTCTTTTTTTTGA[A/G]ACAAAGTCTTGCTGT | 5663 |
rs150575029 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73165399 | CGTTAGCCTCCTGAG[G/T]ACCTGGGACTATAGG | 5663 |
rs150695289 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PSEN1 | GRCh38.p7 | 14:73209439 | GAAAATCAAATGATT[A/G]TCTGTGAGCATGTAG | 5663 |
rs150743438 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PSEN1 | GRCh38.p7 | 14:73213069 | TCAGAACTTTCACTG[C/G]GCATGTTCATGACTT | 5663 |
rs150745286 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73144668 | AAAAGGATAAAGGGA[A/C]TATCATAAATTAGTT | 5663 |
rs150763023 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162346 | GTTAGCAACAGTGTG[A/G]TAAAGTAGGCAATCT | 5663 |
rs150764501 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | PSEN1 | GRCh38.p7 | 14:73191533 | TGAAATTCCAAAATA[C/T]GTACATATATTTTTT | 5663 |
rs150800565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73149926 | AAGCAAATACTGTGA[C/T]GAGCTGCTATAGCCT | 5663 |
rs150816995 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196923 | ATTCTGAATTTTCTT[C/T]CTTTCTTTCTTTTTT | 5663 |
rs150831684 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205215 | GGCGTGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 5663 |
rs150837586 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73136928 | CGTCTTGGGCTGGGT[A/C/T]TGCTTGAGCAACTGG | 5663 |
rs150940566 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171769 | AAAAACATTGCTTTA[C/T]GAGGAAGTTAAGTTT | 5663 |
rs151082255 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73164254 | GGAGAAGCTTAGAAT[A/G]GAGTTCTAGGAGAGG | 5663 |
rs151098329 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204048 | TCATTGCCCAGGCTG[G/T]AGTGCAATGGCACGA | 5663 |
rs151111068 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221086 | ATATTTCTTATAAGA[A/C]CCTAACTTCAAGAGT | 5663 |
rs151150329 | snp | A/T | 0.0322114 | 0.122752 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139192 | GGAGGCTGAGGCAGG[A/T]CAATGGCGTGAACCC | 5663 |
rs151170492 | snp | C/T | 1.64787e-05 | 0.00287038 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73186909 | GTTCTTTTTTTCATT[C/T]ATTTACTTGGGGTAA | 5663 |
rs151205233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73142904 | TCAAGTGTTGTGCTC[C/T]GTCAGTTTGCAGCAG | 5663 |
rs151274214 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | PSEN1 | GRCh38.p7 | 14:73182775 | ATCTGGGAGGTGGAG[G/T]TTGCAGTGAGCCAAG | 5663 |
rs151325212 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | PSEN1 | GRCh38.p7 | 14:73188149 | GGCCAGGATGGTCTC[G/T]ATCTCCTGACCTCGT | 5663 |
rs180823246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181494 | CCAGGTGCAGTGGCA[C/T]GGACCTGTAGACCCA | 5663 |
rs180833819 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73140684 | GGCATTTGCATAGTA[C/T]CTTTACAAAATCCAA | 5663 |
rs180849770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73163501 | AGTACAGGAGACACT[A/G]GAGATCCAGCAAAGG | 5663 |
rs180875304 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173386 | TTTCTTTGAAGCAAT[G/T]TTAGAGTGTAGCTGT | 5663 |
rs180878265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154131 | CATGTTAACTGCTTA[C/T]ATGCGTGCATGAAAT | 5663 |
rs180886992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73202801 | TTTTTAAAACTCAAC[A/G]TCTGTGCTCGCTTTA | 5663 |
rs180898071 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216687 | TCGCTTGAACCTGGG[C/T]GGCAGAGTCTGCAGT | 5663 |
rs181054325 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73164749 | GTTAGAGACTTTTAA[A/G]TTCCAAATTTCACAC | 5663 |
rs181057130 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141522 | TATAGGCTGAGCACA[G/T]TGGCTCACGCCTGTA | 5663 |
rs181081592 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181878 | TCCTGGGTTCAAGCA[A/G]TCCTCCCACCTCAAC | 5663 |
rs181081779 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73203121 | TTCACTCTTGTTGCC[A/C]AGGCTGAAGTGCAAT | 5663 |
rs181101742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73153078 | GACAAAAAGCAAACC[C/T]ATGAGCTATTTAAAG | 5663 |
rs181266679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73167350 | ATGCTCAAAGGAAAT[A/G]CTTATTGGAGTGTTT | 5663 |
rs181270951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73146792 | TTTTTTTATGTAAAT[A/G]TGTATATGGTAATGT | 5663 |
rs181284178 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187459 | CTAGCTCTTAAATTC[A/G]AAGAGGCAGTCAAAC | 5663 |
rs181295963 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73209919 | CCCTCATATTGCAAG[A/C]TATTTAACATCCCTG | 5663 |
rs181390169 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160607 | CTAACGGGTGTAGTT[A/T]TTTTTTGCATTTTTC | 5663 |
rs181420275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197720 | ATCTCATCATTATCT[C/T]TGCAGCTTTCCTTTA | 5663 |
rs181509052 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PSEN1 | GRCh38.p7 | 14:73178975 | GGTCGGTGTGTACTG[C/T]TGAGGATCATATCCA | 5663 |
rs181519087 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | PSEN1 | GRCh38.p7 | 14:73138597 | GAGTCAAGTGATCCT[C/T]CCGCCTTGGCCTCCC | 5663 |
rs181543549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211138 | CAAAGAAGAAATTTA[C/T]TCTTTCACGTGACAG | 5663 |
rs181556440 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221671 | AAGTAATCCACCTCA[G/T]CCTGAGTAGCTGAGA | 5663 |
rs181694247 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73147519 | GCATAGAAAAAGGAA[G/T]GTTGAGAACATTCCT | 5663 |
rs181722099 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73188063 | CCCCCTGAGTAACCG[C/G]GACTACAGGTGCGCA | 5663 |
rs181726819 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222617 | GTGTTCCCGTAGGTT[C/G]TGGAGTCTGAGGATG | 5663 |
rs181785243 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148641 | CTAATCATCATAAAG[A/T]GAGAGCAGAGGCCAG | 5663 |
rs181785527 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73178244 | TTTTTTTTTGAGACC[C/G]AGTCTCGCTTTGTCA | 5663 |
rs181788101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168622 | CTGGCTTCAGGGAAA[A/G]ATCACCTTCTTCCCA | 5663 |
rs181795653 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197142 | GTTTCACCGTGTTAG[C/T]CAGGATGGTCTTGAT | 5663 |
rs181808070 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73159774 | CCATTTTCCATTTCT[C/T]TCAGCCCGTGGCAAT | 5663 |
rs181825217 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73220669 | GTTTCAGGTTATTCT[C/T]GTCAGCTCCACAAAT | 5663 |
rs181919055 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73138410 | ATTTTTAGTAGACAC[A/G]GGGTTTCACCGTGTT | 5663 |
rs181967382 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212036 | AATTGAGAGTGTTAC[A/G]GTCTAATTCTATATC | 5663 |
rs181968931 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73168888 | CTTGGATGCTGCTGC[A/G]GGGCCGCATAGAGCC | 5663 |
rs181981078 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73153456 | GGTTAAACCTCTGAC[G/T]CCAGGGAATCACAAA | 5663 |
rs181985347 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204608 | GCCATTTACAGAAAA[A/G]GTTAGCTGGACATTG | 5663 |
rs181991465 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73182861 | TAAATAAATAAAATT[A/T]AAAAAAGAAATAAAT | 5663 |
rs182212850 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157707 | TGATACTATTTTATA[C/T]AAATAGTATCATACA | 5663 |
rs182221012 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193028 | TTCATTTGAAGATTT[C/T]GGCTGGGCATGGTAG | 5663 |
rs182225444 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73165065 | GGGTTCAAACGATTC[A/G]CCTGCCTCAGCCTCC | 5663 |
rs182230408 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219572 | AGATATGATAGGCCC[A/G]GAAGTTGCTGTGCCC | 5663 |
rs182236740 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PSEN1 | GRCh38.p7 | 14:73175602 | TCCTTTTACTTTGGT[A/G]TGAACATTTTTTCTA | 5663 |
rs182238269 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73195935 | CCTAAACTCTGATCT[C/T]GAATCTGAATCCCAA | 5663 |
rs182240698 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | PSEN1 | GRCh38.p7 | 14:73189383 | TGGGAGGCCGAGGCG[C/G]GTGGTTCACCTGAGG | 5663 |
rs182496163 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216299 | GGGATTAACTGTAAA[C/T]GGGTACAAGGTACCT | 5663 |
rs182508158 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171958 | TGTCCTTTCTCACTT[A/G]TCACAATTTGCAAAT | 5663 |
rs182542137 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143803 | GGGTTGCTTGAGGCC[A/C]GGCAAGACCAGCCTG | 5663 |
rs182558084 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73142053 | GCCTGGGCGACAGAG[C/G]GAGACTCCGTCTCAA | 5663 |
rs182564429 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73186146 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 5663 |
rs182569663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206550 | TAGCAATGTTTTTAT[C/T]GTCTTTCTTTGGTCA | 5663 |
rs182581571 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73165949 | TAATCCCAGCTCCTC[C/G]GGAGGCTGACGCGGG | 5663 |
rs182591718 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73185623 | TGGGGAGAGAGAGGG[A/T]GAGGGAGAGGGAGAG | 5663 |
rs182791530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73189524 | GGCTGAGGCAGGAGA[A/G]TGGCGTGAACCTGGG | 5663 |
rs182805164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73150518 | CCTGTAATCCCAGCA[A/G]TTTGGGAGGCCGAGG | 5663 |
rs182805399 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168906 | GCCGCATAGAGCCTG[C/T]GCCTGCCAGAGAGGA | 5663 |
rs182818456 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212481 | TAAAGTAAAAGATTT[G/T]TTTTTTTAATTGTTC | 5663 |
rs182861388 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205091 | TGTGTTTCTTTCATA[A/C]GTTCTTCAAGAAGCC | 5663 |
rs182864413 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135853 | TAAGTGTGGTATGCT[A/G]TCTAATGAATTAGAC | 5663 |
rs182866626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217944 | AGGTGCCTGCCACCA[C/T]GCCCGGCTAATTTTT | 5663 |
rs182871752 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179264 | ATTTTAGGCTTCTGC[A/C]ACCCACATTACCATC | 5663 |
rs182872826 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73161083 | AGGCTCAAGCAGTCC[C/T]TCCACCTCAGCCTCC | 5663 |
rs182878308 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73138726 | AGCACTTTGGGAGGC[C/T]GTGGCGGGCGGATCA | 5663 |
rs183132973 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162422 | AATTTGGCATGCTCT[C/T]GTTCTCTCTCTCGCT | 5663 |
rs183135415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200330 | GCTGGAGTACAGTGG[C/T]GCAATCTCAACTCAC | 5663 |
rs183137285 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73154881 | TCAGTGAGTTAAAAT[C/T]GATACACTGCTGCTG | 5663 |
rs183147233 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179664 | CTGTCTGGGTGTTAG[A/G]AGACCTCTTTCCTGA | 5663 |
rs183157073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200982 | CTTGAACCCAGGAGG[C/T]GGAGGTTACAGTGAG | 5663 |
rs183163906 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194435 | TTTTTTAAAAAAAAA[A/T]TTTTTTTCAGAGATG | 5663 |
rs183399154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156811 | GCGACTACAGGCGTC[C/T]GCCACCATGCCCAGC | 5663 |
rs183402537 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73175167 | GTCTCGCTCTTGTCC[C/T]GCAGGCTGGAGTGTG | 5663 |
rs183416345 | snp | C/G | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135109 | TGACAAGCATGAGCA[C/G]TTGTAAATGAACAAA | 5663 |
rs183427901 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73195434 | TGCCTCAGCCTCCCA[A/G]AGTGCTGGGATTACA | 5663 |
rs183435766 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73190858 | ATAAATAGATTGTTT[G/T]TGTTTTTGTTTTTTA | 5663 |
rs183436551 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179968 | GCATTTGTACATCTT[A/T]TATCCATCCTTCATT | 5663 |
rs183454938 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151165 | AAAAGAGACATTCCT[A/C]TGTAGAATTTTGGGC | 5663 |
rs183456220 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73223799 | AAAAATTAGCCAGGC[A/G]TGGTGGTGGGCGCCT | 5663 |
rs183641187 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73166380 | TTGATTCCTACCTCT[C/G]CTGTTTTCTGGTTGT | 5663 |
rs183652602 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145920 | GAGACCAGCCTGGCC[A/G]ACATGGTGAAACCCA | 5663 |
rs183685837 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169606 | TCTCATTCATTGCCA[C/T]TCAATCAAGTTTGCT | 5663 |
rs183706774 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139124 | CCGTCTCTACTAAAA[A/G]TACAAAAAATTAGCC | 5663 |
rs183720719 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73213423 | TTTTAAAAAAAAAAA[A/T]GTGAAACTATCAAGT | 5663 |
rs183795600 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73214105 | AACTGATAAGTGGAT[A/G]ATAAATGTGGTATAT | 5663 |
rs183898424 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168032 | TGTTGCCTCTTTGGC[C/T]TGCCATGCCCCTATC | 5663 |
rs183906237 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162097 | GGCAGGAGAATCACT[C/T]TAACCTGGGAGGCCA | 5663 |
rs183915167 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210405 | AGACAGGAAGAGTTA[A/C/T]ATTTGCGTGCACTAA | 5663 |
rs183923258 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187514 | TCTTTGGTAGAGGAT[G/T]AAGGGAAATAACCAC | 5663 |
rs184128355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73170373 | TGCTCTGGTCCAAAC[A/G]CCTCTGACACAAGGA | 5663 |
rs184128468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152478 | TGGGTGTGGTGGCAT[A/G]TACCTGTAGTCCCAG | 5663 |
rs184130140 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73202871 | TGCATGTATTTTTTT[A/T]AAAGTTCTCAAGTCT | 5663 |
rs184146670 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73215326 | TGGTGGCTCACACCT[G/T]TAATCCCAGCACTTT | 5663 |
rs184159218 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73141739 | GCAGTGAGCCATGAT[C/T]GTGGCATTGCATTCC | 5663 |
rs184199596 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73218770 | AGCATAGAGAATGCT[A/C]TTCACCTCTGGGTTT | 5663 |
rs184364208 | snp | A/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220034 | AAGTTTTAACCTCAG[A/G/T]TTCCAAATTCAGTAA | 5663 |
rs184415284 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187248 | ATAAAAACCAAAATA[A/G]TTGATTTTCATACTT | 5663 |
rs184535811 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139529 | AGGTTGCAGTGAGCC[A/G]AGATCATGCCACTGC | 5663 |
rs184548493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208725 | AATGCACCATAAGTT[C/T]TCACTGTGGTCTGTG | 5663 |
rs184563947 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201661 | CATCAAAGATTCCTG[A/T]CTCACAGGCAGAGCA | 5663 |
rs184580869 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162508 | AGCACGCGAACAAGC[A/G/T]ATTGAGTGAGAGAGA | 5663 |
rs184598258 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73170006 | AGGTGGGCAATTCCC[A/G]GAACTGAGGATCCCT | 5663 |
rs184600168 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152005 | CAAGTTCTGCATCCC[A/G]GGTTCACGCCATTCT | 5663 |
rs184632963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73137136 | TCAGATTCTTCTCAC[C/T]GTTGTGGTCAGCTCT | 5663 |
rs184767450 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158308 | TATCTATCTATCTAT[C/G]TATCTATCTATCTAT | 5663 |
rs184799994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196535 | CACCTAGGCAGTGGC[A/G]CCATCTTGGCTCACT | 5663 |
rs184859844 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73202498 | TTTTTTTTTTGAGAC[A/C]GTCTTGCTCTGTCAC | 5663 |
rs184958023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73163523 | CAGCAAAGGTCAATA[A/G]CATGTGCTGTCTTAG | 5663 |
rs185068220 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181745 | ACGTGCAGATAGAAA[A/G]CATGTCTGAAAGGGA | 5663 |
rs185073123 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137904 | AACACGGCGAAACCC[C/T]GGCTCTACAAAAAAT | 5663 |
rs185108056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73177873 | TTGGAGTTCACTGAG[C/T]TTTTTGAATCTCTAG | 5663 |
rs185109877 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73159576 | GTTTCAGCACTGTTT[C/G/T]TTAAAAAAGACTATT | 5663 |
rs185118828 | snp | A/T | 0.000243856 | 0.0110394 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173821 | TTTGTCTTCTAGAGA[A/T]AAGTTAATTTTTAGT | 5663 |
rs185122451 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193882 | GGCTGGTCTTGAACT[C/G]TTGGGCTCAAGCAAT | 5663 |
rs185155161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216760 | CAAAACTCCATCTCA[A/G]AAAAAAAAAAAATAT | 5663 |
rs185196698 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73153257 | AACTTGAAATCTCAA[C/T]GACCTCCAGAGAAAC | 5663 |
rs185341371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216200 | GAGGCATGTATTGTA[C/T]GAGTCATATGAAATG | 5663 |
rs185349736 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171657 | CTAAACTAATTCCAA[C/T]TGGCTAATTTAAAGA | 5663 |
rs185367484 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148914 | CTCCAGCCTGGGCGA[C/T]GAGCGAAACTCCATC | 5663 |
rs185371684 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197277 | AAAGAAAAAGTGCAG[C/T]TGATCGAAAGAAATG | 5663 |
rs185391558 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73189426 | GACCAGCCTGGCCAA[C/T]GTGGTGAAAACCCAC | 5663 |
rs185405511 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73220874 | GGCTTGTGGGGCATA[A/T]CCTTCTTTACCACAG | 5663 |
rs185410776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168894 | TGCTGCTGCGGGGCC[A/G]CATAGAGCCTGCGCC | 5663 |
rs185458725 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181407 | GCGCCATTGCCCTCC[A/T]GCCTGGGCAACAAGA | 5663 |
rs185476526 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73140552 | AAATCTGGCCTAGTT[A/G]TCGTCTTTATTTTCT | 5663 |
rs185602931 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73163100 | ACAGCACATTTAGAC[A/T]GAATACAGTCTTTAA | 5663 |
rs185668881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73140819 | ACATAACCATTATTT[A/G]AAAACAAGTTGCTAT | 5663 |
rs185679892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73161880 | TGTTTATAGGCCGGG[C/T]GCAGTGGCTCACGCC | 5663 |
rs185681891 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73138728 | CACTTTGGGAGGCCG[A/T]GGCGGGCGGATCATG | 5663 |
rs185695724 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212676 | AGGATATTGGCAGAA[A/C]TGCAAGTATTTCTTC | 5663 |
rs185698561 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223015 | ATCCTTGTGATCTTC[A/T]CACCTCTTTAAATTC | 5663 |
rs185710970 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179354 | GGGTGTGGTGGCTCA[C/T]GCCTGTAATCCTAAC | 5663 |
rs185718364 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73199387 | CTACAGGAAGTAGAG[A/G]AAAATAGTGGAAAAT | 5663 |
rs185722644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73166234 | AACCAGATCATCCAG[C/T]TGGGGACTCTGAATG | 5663 |
rs185742783 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73207783 | AGCTGGACCCCATGC[C/T]TGCCAAAGGCAAGCC | 5663 |
rs185848749 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187118 | TCCTTGCTTATAATA[A/G]GTAGAACTGAAAGAA | 5663 |
rs185859124 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145112 | TGGCCAGGCTGGTCT[A/C]GAACTCCTGGCCTCA | 5663 |
rs185909059 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154454 | AAAAAAGTGAAAATT[A/C]GTGGGGTGTGGTAGT | 5663 |
rs185914980 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73164764 | ATTCCAAATTTCACA[C/T]ACTATGATTTCACCC | 5663 |
rs185931538 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141562 | AAGGTGGTGGATCAC[C/G]TGAGGTCAGGAGTTC | 5663 |
rs185954734 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73182339 | AAAAAAAAAAAATTA[A/G]AAAATTAGCCAGGCA | 5663 |
rs186019236 | snp | A/C/T | 0.00239393 | 0.0345281 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160240 | ATGTGACAAGATTTC[A/C/T]TTTTTAAGGGCTGAA | 5663 |
rs186116398 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73138544 | TTTTTTAGAGATGGG[A/T]GCCTCACTATGTTGC | 5663 |
rs186137543 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73178566 | GTTTATTTTCCAATT[G/T]TTTTCACTATTGTTC | 5663 |
rs186170275 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73212143 | TTGAGACAGAGTCTC[A/G]CTCTGTCGCCAGGTT | 5663 |
rs186286344 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179121 | TTCCTGCAGCCAAAA[C/G]TGGACTTTATCTTCC | 5663 |
rs186306182 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73138602 | AAGTGATCCTCCCGC[A/C]TTGGCCTCCCAGAGT | 5663 |
rs186309281 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222343 | GCTTTTAAAAACCCT[C/T]CTTTTGCAATAGATG | 5663 |
rs186363196 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73153645 | ATTGTAGAAATTCAA[A/G]CAATATCCATTAAGT | 5663 |
rs186380728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193305 | ATAGAACAAGACCTT[A/G]TCTCAAAAAAAATTT | 5663 |
rs186455457 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160611 | CGGGTGTAGTTTTTT[A/T]TTGCATTTTTCTAAT | 5663 |
rs186495252 | snp | A/C/G | 0.000282978 | 0.011892 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73198104 | GGAGAGAAATGAAAC[A/C/G]CTTTTTCCAGCTCTC | 5663 |
rs186531618 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219582 | GGCCCGGAAGTTGCT[C/G]TGCCCCATCAGCAGC | 5663 |
rs186543682 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211560 | TGTGGGAGGGGGTGG[A/G]AACCCAAACAATTCA | 5663 |
rs186548107 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196233 | TCTTTAAGGGAGAGT[A/G]TATCATAAAACTGAA | 5663 |
rs186549864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168844 | CCATCCCCGAATGGC[C/T]GCGTTGAAGGAGCAT | 5663 |
rs186597939 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73142212 | GCCCATTCATAACAT[G/T]AGAAGTTGGGCCGCC | 5663 |
rs186635755 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PSEN1 | GRCh38.p7 | 14:73165784 | AGTGTGTGGCCGGGC[A/G]CGGTGGCTCACGCCT | 5663 |
rs186750334 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73170041 | TTTTTAGACCATACA[A/C]GGTAACTTCCGGACG | 5663 |
rs186752250 | snp | A/G | 0.0349115 | 0.127424 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223319 | ACCCTGAGCCCTGAC[A/G]TGTGGTGGCAGCATT | 5663 |
rs186756046 | snp | C/G/T | 0.00398755 | 0.0445055 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152163 | GTGATTCGCCCGTCT[C/G/T]GGCCTCCCAAAGTTT | 5663 |
rs186766221 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73214285 | CCTGTAATCCCAGCA[C/G]TTTGGAAGGCCAAGG | 5663 |
rs186773784 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSEN1 | GRCh38.p7 | 14:73191205 | GACCAGATTCCCACC[A/G]CCTAAAGATAAGTCC | 5663 |
rs186786315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73188124 | AGTAGAGACAGAGTT[C/T]CACCATGTTGGCCAG | 5663 |
rs186858518 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73155481 | ATATTTATATGTCTA[G/T]CATAGAATCAAATAT | 5663 |
rs186894936 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194598 | TTTCAAGACGGAGTC[C/T]GGCTCTGTCGCCCAG | 5663 |
rs187040561 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73174972 | CATACCTTAGAAAAA[A/C]TTACACATTATCACA | 5663 |
rs187098525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73218343 | CTGCCTGCCTCAGCC[A/G]CATAAAGTGCTGGGA | 5663 |
rs187122943 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73189737 | TCTACGAGTAAACAA[G/T]AATTGTGCAAGCCCT | 5663 |
rs187128252 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141894 | AACACAGTGAAACCC[C/T]GTCTCTACTAAAAAT | 5663 |
rs187129440 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169420 | TGAGGCTATAGAGAC[C/G]AGTGACTTCCTCTGA | 5663 |
rs187155003 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216302 | ATTAACTGTAAACGG[G/T]TACAAGGTACCTGAC | 5663 |
rs187161582 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73183149 | TTGAGATGGAGTCTC[C/G]CTCTGTTGCTCAGGC | 5663 |
rs187172458 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162450 | GCTCGCTCGCGCGCT[C/G]TCTCTCTCTCTCTCC | 5663 |
rs187295663 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73165202 | CTCGGGTGATCCGCC[C/T]GCCTCAGCCTCCCAG | 5663 |
rs187338631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204753 | ATGGAAATCCATAAA[C/T]AGGCTGGGTGCAGTG | 5663 |
rs187394757 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181271 | ATGGAGAAATCCTGT[C/G]TCTACTAAAAATACA | 5663 |
rs187400464 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73201975 | TGGCCTTGAACTCCC[C/T]ACCTCAAGTGATCCA | 5663 |
rs187459198 | snp | C/G | 0.0349115 | 0.127424 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205815 | TGTGTATATCTAGAT[C/G]TAGATTGATATATTG | 5663 |
rs187467579 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136187 | TTAAATTTAGGATGG[A/C]CATCGCTTGTATGCC | 5663 |
rs187489510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73175656 | CTATGGCTATGAGAT[A/G]TTTGATTCAAGTGCC | 5663 |
rs187585839 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143884 | GTCCCACCTGCTTGG[G/T]AGGCTGAGGTGGGAG | 5663 |
rs187601578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186402 | AAAAAAGAATATTCA[A/G]ATGTCCAAGGAGTAC | 5663 |
rs187618307 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73166025 | TGTGCCACTACTAGG[C/T]GACAGAATGAGACTC | 5663 |
rs187635823 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73206727 | CATGGAAAGGTTCAG[A/G]CTGAGGTTATGATTT | 5663 |
rs187662338 | snp | G/T | 0.0387552 | 0.1337 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162098 | GCAGGAGAATCACTC[G/T]AACCTGGGAGGCCAA | 5663 |
rs187665814 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73147753 | AAATGAATTTACTAG[A/G]ATTTAACTAACAATG | 5663 |
rs187683342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200336 | GTACAGTGGCGCAAT[C/T]TCAACTCACTGCAAC | 5663 |
rs187700127 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157799 | ACTTGAGGCCACCTG[A/G]CCAACATGAAACCCC | 5663 |
rs187705894 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73185791 | CCTGGCCTCATGATC[C/T]GCCTGCCGTGGCCTC | 5663 |
rs187725305 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156905 | CTGACCTTGTGATCC[A/G]CCCGCCTGGGACTCC | 5663 |
rs187725435 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73175288 | CCTGCCACCACACCC[A/G]GCTAATTTTTGTATT | 5663 |
rs187737228 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135207 | CTTCTCCCACAACTT[A/C]TCTTTCATTCTGCTA | 5663 |
rs187743142 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219338 | TCTTTGACTATAACA[A/G]AATCTGGGGAGGACA | 5663 |
rs187756689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195529 | ACTCCTATGTCAGTT[A/G]TGAAGATTAAATTAA | 5663 |
rs187950172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73150839 | CTTTGGGAGGCCGAG[A/G]AGGGCGGATCACGAG | 5663 |
rs187950877 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139175 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 5663 |
rs187976554 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73180133 | GGGATTACTGGGACA[C/T]GCCACCATGCCTGGG | 5663 |
rs187980167 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73179800 | CTAGTACTTCTAATT[A/C]CCCAGCCCACCTACC | 5663 |
rs187994085 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73224155 | GTAAACTTATAAGAC[A/G]TATGTTGTACAGTGC | 5663 |
rs188003078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73167042 | TGTTTTCTTCTTTTT[C/T]GTATCTTTTGAAATT | 5663 |
rs188019149 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73146102 | CAGAGCAAGACTGTG[C/T]CTCAAAATAAAGACA | 5663 |
rs188046689 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187281 | ATATTGTTTTTTATC[A/G]GTGACTCTTTTTTCT | 5663 |
rs188202564 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169807 | TGTGCCACCATGCCC[A/G]ACTAATTTTTATATT | 5663 |
rs188214574 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221269 | AGATTCATTCCCTCT[C/T]TCAGACATGTGCTAG | 5663 |
rs188246722 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PSEN1 | GRCh38.p7 | 14:73213448 | TCAAGTATTGCTCCT[C/G]CTAACTTCAGATCAG | 5663 |
rs188247683 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201173 | GGCTCACTGCAAGCT[C/T]CGCCTCCTGGGTTCA | 5663 |
rs188440882 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193374 | ATATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 5663 |
rs188449361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154079 | TATTCAGACTATAAA[C/T]ATATCAGCATAATTG | 5663 |
rs188449539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173239 | GCAGAATCTGGTTCT[A/G]TAACAAGTTCCTAAT | 5663 |
rs188468120 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216320 | CAAGGTACCTGACTG[G/T]GGCAATGGACATGTG | 5663 |
rs188495286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73190883 | TTTTTAGTTTGAGGA[C/T]ACTGGAAATGCTTAA | 5663 |
rs188499568 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151512 | TGATCTTGGTGATTT[C/T]CCCCTTTCATTTTCT | 5663 |
rs188549491 | snp | G/T | 0.0345262 | 0.126772 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216069 | CCATCAACTGGTAAA[G/T]GGATAAGCAAACCAT | 5663 |
rs188553604 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181754 | TAGAAAACATGTCTG[A/C]AAGGGAAACGGTTTT | 5663 |
rs188555599 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73163935 | TCATTTTGTTTAAAA[A/G]AAAAAAATCATCCTG | 5663 |
rs188558992 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73140929 | GGTAGATGTGTGGAT[C/T]GGTGAGGGCAGTTCT | 5663 |
rs188569354 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73191748 | TGATAGAGTCTCACT[G/T]TGTTGCCCAGGCTCG | 5663 |
rs188756198 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134477 | GGGTGGACCATAATT[G/T]ATTGTACCACATTTA | 5663 |
rs188757023 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187164 | AATTCTAAGCCTTTT[C/T]GAAGATTATATAGTC | 5663 |
rs188774620 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145189 | TGAGCCACTGCGTCC[A/G]GCCTACTTACCTTTT | 5663 |
rs188903613 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73139874 | GAAAAAGGTATTAGT[A/G]TTGGCTTTTCACAAC | 5663 |
rs188936594 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73163009 | TTAAACAAATAAATT[A/G]TACTTTTTTTGAAGA | 5663 |
rs189035621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73166285 | ATGCTAGACTTAGCT[A/G]ATTAAACTGTTCATA | 5663 |
rs189048639 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73178583 | TTTCACTATTGTTCT[G/T]GTTAGATAATTTCTA | 5663 |
rs189066708 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168567 | ACGTGGCTAACTTCA[C/G/T]ATGGTGCAGCTTTGG | 5663 |
rs189067308 | snp | C/T | 0.000362056 | 0.0134498 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208817 | GGAACTTCCCCTTTC[C/T]GCCTAGGAGCCTGTC | 5663 |
rs189068922 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73138553 | GATGGGAGCCTCACT[A/G]TGTTGCCCAGGCTGG | 5663 |
rs189070347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208495 | AATCCTCAGTGGAGA[G/T]GAGACCCGGAATGGG | 5663 |
rs189083686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210878 | TGAACTTCACTTATA[C/T]ATTTTAATTATTTTT | 5663 |
rs189105648 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187654 | GTACAGAAAGTTACT[A/G]AAGAAGTTTCCACCC | 5663 |
rs189176906 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137804 | AAATAAAATGTGAGG[C/G]CCGGGGCGGTGGCTC | 5663 |
rs189316297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73163312 | GCTGGACTCGATGGC[C/T]CATGCCTGTAATCCC | 5663 |
rs189334594 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73202618 | GCTGGGACTCTAGGC[A/G]CCCGCCACCATGCCT | 5663 |
rs189346757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160261 | AAGGGCTGAATAATA[C/T]TCTGTGTTATGTATA | 5663 |
rs189444451 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | PSEN1 | GRCh38.p7 | 14:73138405 | TTTGTATTTTTAGTA[A/G]ACACGGGGTTTCACC | 5663 |
rs189472757 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73178109 | ATTTTTAGTAGAGAC[A/G]GGGTTTTACCACATT | 5663 |
rs189478517 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197124 | TTTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT | 5663 |
rs189488874 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73159721 | AAAAACTGAAACTCT[A/G]TACTCATTGGACAAC | 5663 |
rs189507244 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220214 | AGCAGTCTTTTTCTA[C/T]AGCCAGTAAGGCAGC | 5663 |
rs189592492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181440 | AAAACTCCATCTCAA[A/G]ATCAATCAATCAATC | 5663 |
rs189601896 | snp | A/G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73140555 | TCTGGCCTAGTTATC[A/G/T]TCTTTATTTTCTTTT | 5663 |
rs189731347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73149932 | ATACTGTGACGAGCT[A/G]CTATAGCCTGGAAAA | 5663 |
rs189747954 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73189469 | TACAAAAAATTAGCC[A/G]GGCGTGGTGGTGGGT | 5663 |
rs189770284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168897 | TGCTGCGGGGCCGCA[C/T]AGAGCCTGCGCCTGC | 5663 |
rs189788376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212174 | GGAGTGCAATGGTGC[A/G]ATCTTGGCTCACTGC | 5663 |
rs189861859 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73170713 | AACTCATAGTGACGG[G/T]TCTGTTGTTAATCCC | 5663 |
rs189877321 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216270 | CTGGTTGCTTAAGGC[C/T]TAGGGTAGGAGTGGG | 5663 |
rs189879430 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171747 | ATGAGGGTGGAGCAG[A/G]TAATGGAAAAACATT | 5663 |
rs189892939 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73203099 | GTTTTTGTTTTTGAG[A/G]TGGAGTTTCACTCTT | 5663 |
rs190062601 | snp | A/T | 0.0437281 | 0.141251 | intron-variant | PSEN1 | GRCh38.p7 | 14:73213412 | TCGTCTCCAACTTTT[A/T]AAAAAAAAAAAGTGA | 5663 |
rs190092338 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158442 | GTGATTCTCCTGTCC[C/G]AGCCTCCCCAGTAGC | 5663 |
rs190095457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73153363 | TAACATAACAGCCCC[A/G]TAAGTGTTCAGTATT | 5663 |
rs190112607 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196936 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTG | 5663 |
rs190271846 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143702 | TGTTAGCATAGGGTA[A/G]AAATGGAAACTACTT | 5663 |
rs190296731 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186111 | ATGTTGGCTAGGTGC[A/G]GTGGCAACCTGTAAT | 5663 |
rs190300744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206299 | ATTAGGAAGACTGGC[A/G]ATTTGTGTGGAGAAA | 5663 |
rs190307334 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73165948 | ATAATCCCAGCTCCT[C/T]GGGAGGCTGACGCGG | 5663 |
rs190315377 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217387 | GATAATTGGACCTCA[C/T]CTTAGTAGTTCTCTA | 5663 |
rs190372534 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73147338 | TCTTAAGCAAGTCAC[G/T]GAACTTCTCTGGATT | 5663 |
rs190378288 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73165049 | GCAACCTCTGCTTCC[C/T]GGGTTCAAACGATTC | 5663 |
rs190384957 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73177135 | CTAACCAGCCATGAC[G/T]CTCAGATGATGGACT | 5663 |
rs190402057 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219887 | TGAGACTTGTTTTCC[C/T]CTCTCTTTGAGTCAA | 5663 |
rs190403365 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204040 | TTTCGCTCTCATTGC[C/T]CAGGCTGGAGTGCAA | 5663 |
rs190413772 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73182508 | TCTCAAAAAATAATT[A/T]AAAAAAAAATATTTG | 5663 |
rs190415820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156518 | GATTTGCCTCAAAAT[A/G]ATACTGGAGTGGCAA | 5663 |
rs190653425 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73161006 | ATACAAGGTTTTACT[C/G]TGTCACCCAGGCTGG | 5663 |
rs190669428 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | PSEN1 | GRCh38.p7 | 14:73138696 | CCGAGCGCGGTGGCT[C/T]ACCCCTGTAATCCCA | 5663 |
rs190718487 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223402 | TTCCTTTTGAAATAC[A/G]TAATTGTTGAGACTA | 5663 |
rs190822666 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73190459 | GTGCCCTCTATCCAG[A/G]GTGACAGTCAGACCT | 5663 |
rs190928472 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73162052 | GGTGTGGTGATAAGT[A/G]CCTGTAATCCCAGCT | 5663 |
rs190932247 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73138975 | CTGTCAAGAAAAAAA[A/G]AAAAAAAATGTAAAA | 5663 |
rs190950740 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223186 | CTCTAACGGGAAACA[C/T]CTCAGATTTGCATAT | 5663 |
rs190953913 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204779 | CAGTGGCTCATGCCT[A/G]TAATCCTAGCACTTT | 5663 |
rs190958493 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73179491 | GCATGGTGGTGGGCA[C/T]CTGTAGTTCCAGTTA | 5663 |
rs190959929 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200747 | GTTGAGTTACTGGAA[A/G]AGCAGTTTCAAGAAG | 5663 |
rs190961956 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73199848 | CCTCCTGGGTTCAAG[C/G]AGTTCTCCTGCCTCA | 5663 |
rs190973507 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73165520 | GGAGGCCGAGGTGGG[C/T]GGATCACCTGAGGTC | 5663 |
rs191185801 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141895 | ACACAGTGAAACCCC[A/G]TCTCTACTAAAAATA | 5663 |
rs191214678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152456 | AAAAAAAAAAAAAAA[A/G]AGTCAATGGGTGTGG | 5663 |
rs191216861 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73170042 | TTTTAGACCATACAA[G/T]GTAACTTCCGGACGT | 5663 |
rs191218391 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193954 | GAGCCACTGCATCTG[G/T]CCTCAATTCACTTTT | 5663 |
rs191221691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73185607 | AGGGAGAGGGAGACC[A/G]TGGGGAGAGAGAGGG | 5663 |
rs191222414 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73154684 | TGAAATATATGACAG[A/T]TATATCCCAATATAC | 5663 |
rs191233062 | snp | A/C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73214728 | AATACTGTATGATTC[A/C/T]ACTTACATCAGAGTA | 5663 |
rs191245695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73191229 | TAAGTCCTGTCATCC[C/T]TTCAGGAATTAATAT | 5663 |
rs191448811 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73174123 | TTATTTTGGATTTCA[A/G]TGCCTTTTTAGGCCA | 5663 |
rs191461905 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73175450 | GGTTTGAGACCAGCC[C/T]GAGCAACATAGTAAG | 5663 |
rs191464024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157016 | TTAAGTCATCATTCT[C/T]ATATTTAGCTACCAA | 5663 |
rs191493181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73175148 | TTTTTTTCCCCGAGA[C/T]GAAGTCTCGCTCTTG | 5663 |
rs191511359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216155 | GTATCATGGTTAAAC[C/T]TCAAAAACATTATAT | 5663 |
rs191527044 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73218767 | CACAGCATAGAGAAT[G/T]CTCTTCACCTCTGGG | 5663 |
rs191630738 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73180142 | GGGACACGCCACCAT[G/T]CCTGGGTAATTTTTG | 5663 |
rs191632202 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162499 | GAGAGAGAGAGCACG[C/T]GAACAAGCGATTGAG | 5663 |
rs191767599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169598 | GCTAGAAATCTCATT[C/T]ATTGCCACTCAATCA | 5663 |
rs191776809 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195104 | GTAACCATCTATTCT[A/T]GCTTAGCTGTGAGTA | 5663 |
rs191965727 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148412 | CTCTTATTCTTCTAC[A/G]GCTGAGTCCATTTTA | 5663 |
rs192001236 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73189174 | CAGGAGAAAGAAATA[C/T]GAACTATATAATTTG | 5663 |
rs192042980 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179216 | CTCGGGACTGACATT[C/G]TTCCAGTCAGAGTAA | 5663 |
rs192063907 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222420 | AGTGTATGTATTCTC[A/G]ATATAACTTGTAGAG | 5663 |
rs192084864 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151017 | AGCTTGCAGTGAGCC[A/G]AGATTGCACCACTGC | 5663 |
rs192093348 | snp | C/T | 3.29669e-05 | 0.00405984 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186819 | TTAAGGGTTGTGGGA[C/T]CTGTTAATTATATTG | 5663 |
rs192095144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137807 | TAAAATGTGAGGCCC[A/G]GGGCGGTGGCTCACG | 5663 |
rs192126749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73207115 | TGAGCTAAGGAGTTC[C/T]GGATTACCCTGGGCA | 5663 |
rs192126858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158790 | TTTAAGGTACTACCA[A/G]AGAACTTTCCAAACT | 5663 |
rs192128855 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73177385 | TGCTGGGGTTTTTTT[G/T]TGTGTGTGTTTTTGT | 5663 |
rs192229600 | snp | A/T | 0.0562307 | 0.157967 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139287 | GACTTCGTTTTTTTT[A/T]TAAAAAAAGGCTGGG | 5663 |
rs192266119 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179872 | TTCTGCCCAGGTTTT[A/G]TAACTGTATTCAGTG | 5663 |
rs192302611 | snp | A/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219455 | TTGCACTATTGGACT[A/T]TGGAAGGAGGTGCCT | 5663 |
rs192323592 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195791 | AAAGTGCTGAGATTA[C/T]AGGTGTGAGCCACTA | 5663 |
rs192325351 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211670 | TGGTTTAAGGGCCAG[C/G]TAGTTACAATGACAG | 5663 |
rs192327928 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139342 | GCCAGCACTTTGGGA[G/T]GCCGAGGCAGGTAGA | 5663 |
rs192334091 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168887 | ACTTGGATGCTGCTG[C/T]GGGGCCGCATAGAGC | 5663 |
rs192535794 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201375 | ACAGGCGTGAGCCAC[C/T]GCGCCTGGCCGAGAA | 5663 |
rs192578722 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181302 | AAAAAATTAGCTGGG[C/T]GTGGTGGCGAGTGCC | 5663 |
rs192588234 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73163066 | TCATCTGTAGATTCT[G/T]ATGTCACATTTTACT | 5663 |
rs192607602 | snp | A/T | 0.0256215 | 0.110247 | intron-variant | PSEN1 | GRCh38.p7 | 14:73202420 | TATCTATCACATACT[A/T]TATATATATATATAT | 5663 |
rs192637254 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162165 | GCCTGGGCAACAGGA[G/T]CAAAACTCCATCTCA | 5663 |
rs192732516 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158276 | AGGTGTATATTTAAC[A/T]TTTTTTTCTATCTAT | 5663 |
rs192744171 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73196407 | TATATTATAGTTCTA[A/T]ATATACTATATTATA | 5663 |
rs192837807 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192374 | TGATCTCCGGAGGTA[A/G]AGACTGCAGTGAGCC | 5663 |
rs192876830 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73144573 | AGGCAATATAGTGTA[C/T]TCTGTGAATTCCAAC | 5663 |
rs192897390 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219961 | CTGACACTCATTACC[A/G]TCTGTGATTGCCATT | 5663 |
rs192945742 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136460 | AACGGTGAGGGTTCT[C/T]GGGCGGGGCCTGGGA | 5663 |
rs192955858 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219703 | CGGAACTCTTCATCT[C/T]AAACTACACGTTGAA | 5663 |
rs192957146 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73176456 | TCTTTCTTATAATCT[A/G]GAATTTACATTCAGA | 5663 |
rs193003623 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73166331 | GCTGTGGTGCCATAG[A/T]AAGAAAACAAGTTTT | 5663 |
rs193025906 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208509 | AGGAGACCCGGAATG[A/G]GTATCTCCTATCCAC | 5663 |
rs193082561 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73166098 | AAAGTAGTATCCAGC[A/G]TACTACAAAGAGGAA | 5663 |
rs193085562 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197037 | TCCCGGGTTCACGCC[A/G]TTCTCCTGCCTCAGC | 5663 |
rs193115013 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151513 | GATCTTGGTGATTTC[C/T]CCCTTTCATTTTCTA | 5663 |
rs193122053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73191109 | CCCAGAATTAAAATA[A/G]CATTTTCTTCATTAT | 5663 |
rs193206415 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187169 | TAAGCCTTTTTGAAG[A/G]TTATATAGTCTTCTA | 5663 |
rs193207548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145846 | TCGTGGTGGCTCACA[C/T]CTGTAATCCTAGCAC | 5663 |
rs193266056 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169857 | CACCATGTTGGCCAG[G/T]CTGGTCTCAAACTCC | 5663 |
rs193266824 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73139990 | ATTAGACGTAAATAA[C/T]CATTTTTCATTAAAA | 5663 |
rs193278015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73213533 | TAGCATTCAGCACAC[A/G]TGTCACCATCTCTGA | 5663 |
rs199499966 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73208850 | CCTCCTGCTGCCATC[A/T]ACCTGCTGTCTATAG | 5663 |
rs199507975 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73196932 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 5663 |
rs199511478 | in-del | -/A/AA | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154444 | TCTACAAAAAAAAAA[-/A/AA]GTGAAAATTAGTGGG | 5663 |
rs199564632 | snp | C/T | 0.00199792 | 0.0315431 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73170952 | ATATGGCGCCAAGCA[C/T]GTGATCATGCTCTTT | 5663 |
rs199573803 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73138967 | CCAGACTCTGTCAAG[-/A]AAAAAAAGAAAAAAA | 5663 |
rs199597924 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73136865 | GCAGGTGCCTTGGGC[C/T]GGGATTAGTAGCCGT | 5663 |
rs199632597 | snp | A/G | 6.58968e-05 | 0.00573969 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73219232 | TTTCTACTTTGCCAC[A/G]GATTATCTTGTACAG | 5663 |
rs199634340 | snp | G/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73136950 | AGCAACTGGTGAAAC[G/T]CCGCGCCTCACGCCC | 5663 |
rs199636562 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73220440 | TTTGCTTTTGCCACA[C/T]AGTAGCTCAGAATTT | 5663 |
rs199637432 | snp | C/T | 1.64776e-05 | 0.00287028 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73186873 | CCATGCCTGGCTTAT[C/T]ATATCATCTCTATTG | 5663 |
rs199643125 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219554 | TGAGGGACGAGGTCA[A/G]GGAGATATGATAGGC | 5663 |
rs199648497 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73147904 | TTAATGTAATCTATG[A/G]AAGTGTTTTTTATAA | 5663 |
rs199658581 | snp | A/C | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220181 | GCCTCCTCTGTCCTC[A/C]TTCTTCTCTCCCACA | 5663 |
rs199676539 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220299 | GAAAAGAATGTGTTA[C/T]GAATCGGTGCTGTCA | 5663 |
rs199680675 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136528 | AAAACAGCGGCTGGT[C/T]TGGAAGGAACCTGAG | 5663 |
rs199689757 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136482 | GGCCTGGGACAGGCA[C/G]CTCCGGGGTCCGCGG | 5663 |
rs199703896 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73219091 | GCCTGAAAATGCTTT[C/T]ATAATTATGTGTGAA | 5663 |
rs199708160 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73220413 | AAGCACTTTCTGTCC[C/T]GGTATTTTGTTTTTG | 5663 |
rs199709800 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73137148 | CACCGTTGTGGTCAG[C/T]TCTGCTTTAGGCATA | 5663 |
rs199715992 | snp | A/G | 8.23825e-05 | 0.00641751 | missense | PSEN1 | GRCh38.p7 | 14:73211891 | CCTGAGTCACGAGCT[A/G]CTGTCCAGGAACTTT | 5663 |
rs199723282 | snp | G/T | 0.0401596 | 0.135893 | missense | PSEN1 | GRCh38.p7 | 14:73198043 | TAGATTTAGTGGCTG[G/T]TTTGTGTCCGAAAGG | 5663 |
rs199723458 | snp | A/C/G | 0.000153988 | 0.00877328 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173743 | TTTGCTTTCCACCCT[A/C/G]TTCTTCTTATGGTTG | 5663 |
rs199726791 | snp | A/C | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219830 | GTGGGCAGGGGTTCC[A/C]GCTTCCCTTTGATTT | 5663 |
rs199738569 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219518 | GTGGACTGTGTCCCT[C/T]GGTGCAGAAACTACC | 5663 |
rs199740663 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73211861 | GACAGTCATCTAGGG[C/T]CTCATCGCTCTACAC | 5663 |
rs199742610 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73186840 | AATTATATTGAAATG[C/T]TTTCTTTTCTAGGTC | 5663 |
rs199748273 | snp | C/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73136914 | GGAGAAAGAGGAAGC[C/G]TCTTGGGCTGGGTCT | 5663 |
rs199759123 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219489 | GAAAACGATTTTGAA[C/T]ATACTTCATCGCAGT | 5663 |
rs199759305 | snp | C/G/T | 8.34598e-05 | 0.00645939 | missense | PSEN1 | GRCh38.p7 | 14:73148066 | TCCAGAATGCACAGA[C/G/T]GTCTGAGGACAACCA | 5663 |
rs199765230 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73137100 | TGTCCAGTGACTCTT[A/G]TGTTTGCTGCTGCTT | 5663 |
rs199780620 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73158332 | TATCTATCTATCTAT[C/T]TATTTTTAAGACGGA | 5663 |
rs199791466 | in-del | -/TAA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73166072 | TAATAATAATAATAA[-/TAA]AATAAAAATAAAAGT | 5663 |
rs199797974 | in-del | -/TGAT | 0.00438332 | 0.0466095 | intron-variant | PSEN1 | GRCh38.p7 | 14:73166991 | ATACCGCAGACTGGG[-/TGAT]TGATTTATTTATTTA | 5663 |
rs199801341 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219651 | AACTCTCAGGACTAC[C/T]GTTACCAAGAGGTTA | 5663 |
rs199803714 | snp | C/T | 3.29516e-05 | 0.00405891 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73219271 | GGACCAATTAGCATT[C/T]CATCAATTTTATATC | 5663 |
rs199805471 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219409 | TCCCGGCTGGACTTT[C/T]GCAGCTTCCTTCCAA | 5663 |
rs199811023 | snp | C/T | 3.38306e-05 | 0.00411269 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171069 | ATGAGTTTTGTTTTA[C/T]TATTCTCAAAGCCAG | 5663 |
rs199812637 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136555 | TGAGCTACGAGCCGC[A/G]GCGGCAGCGGGGCGG | 5663 |
rs199825768 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73190487 | CCTTGTCTCTATTTA[A/T]AAAAAAAAAAAAAAA | 5663 |
rs199842082 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | PSEN1 | GRCh38.p7 | 14:73192774 | CAGCAGGCATATCTC[A/G]TTATGATTAGTGCCC | 5663 |
rs199852640 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73153677 | ATTTTTTTTTTTTTT[G/T]CCCATTAAGTCTTAA | 5663 |
rs199951212 | snp | A/G | | | missense | PSEN1 | GRCh38.p7 | 14:73173612 | ACTGTGGGCCAGAGA[A/G]CCCTGCACTCAATTC | 5663 |
rs199951672 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219889 | AGACTTGTTTTCCCC[C/T]CTCTTTGAGTCAAGT | 5663 |
rs199959407 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198160 | GGATATTGAATTAGT[A/G]ATCAGTGTAGAATTT | 5663 |
rs199959804 | snp | A/G | | | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136796 | GGCCGGGTGGAGAGA[A/G]ATTCCGGGGAGCCTT | 5663 |
rs199965160 | in-del | -/AT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73174072 | GTAAAATATATATAT[-/AT]TATGATTAGTTATCA | 5663 |
rs199976379 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73137173 | GGCATATTAATCCAT[A/G]GTGGAGGCTGGGATG | 5663 |
rs199988688 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73137010 | CATTCTGGGCGAAGT[C/T]CGCACGCCTCTTGTT | 5663 |
rs200007795 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73136985 | TGTGTCCTTGTCCAG[A/G]GGCGACGAGCATTCT | 5663 |
rs200010823 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136416 | TCCGTGGGCCGGCCG[C/G]CAACGACGCCAGAGC | 5663 |
rs200017951 | snp | C/T | | | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73211926 | CAGTATCCTCGCTGG[C/T]GAAGACCCAGAGGAA | 5663 |
rs200019561 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220310 | GTTATGAATCGGTGC[C/T]GTCAGCCCTGCTGTC | 5663 |
rs200022075 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73148155 | GACTGGATTCACTTA[C/T]CATCTCCCCTCACCT | 5663 |
rs200048785 | in-del | -/C | 0.0267878 | 0.112589 | intron-variant | PSEN1 | GRCh38.p7 | 14:73140333 | CTTCTGCCTCAGCCT[-/C]CCGAGTAGCTGGGAC | 5663 |
rs200058399 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73173536 | CTCCATTAACACTGA[C/T]CTAGGGCTTTTGTGT | 5663 |
rs200065583 | snp | A/G | | | missense | PSEN1 | GRCh38.p7 | 14:73192679 | ACGTTGCTGTGGACT[A/G]CATTACTGTTGCACT | 5663 |
rs200067194 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219617 | CGCGTGGTCACAGGA[C/T]GATTTCACTGACACT | 5663 |
rs200067880 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73213407 | CTCTTCGTCTCCAAC[-/T]TTTTAAAAAAAAAAA | 5663 |
rs200082315 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136573 | GGCAGCGGGGCGGCG[C/G]GGAAGCGTATGTGCG | 5663 |
rs200088445 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73190482 | CAGACCTTGTCTCTA[-/T]TTTAAAAAAAAAAAA | 5663 |
rs200102622 | snp | A/G | 1.64988e-05 | 0.00287213 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186961 | CTTTCAGAATTAACT[A/G]CCTTTGTGCTGTGTA | 5663 |
rs200104200 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73136969 | CGCCTCACGCCCCGG[A/G]TGTGTCCTTGTCCAG | 5663 |
rs200107446 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219581 | AGGCCCGGAAGTTGC[C/T]GTGCCCCATCAGCAG | 5663 |
rs200133012 | snp | A/C | 1.65007e-05 | 0.00287229 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217082 | TTGTGAAATCATAGC[A/C]AAGAGTGACCAACTT | 5663 |
rs200141310 | snp | A/G | 1.64819e-05 | 0.00287066 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73170925 | GGAAGAAGATGAGGA[A/G]CTGACATTGAAATAT | 5663 |
rs200142391 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73198176 | ATCAGTGTAGAATTT[A/G]TCGGAACTGAAGCAC | 5663 |
rs200150596 | snp | A/G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136475 | CGGGCGGGGCCTGGG[A/G/T]CAGGCAGCTCCGGGG | 5663 |
rs200157024 | snp | G/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220381 | GGTAGAATTAAAGAA[G/T]AGTAAAATGGCTGTT | 5663 |
rs200159291 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73217266 | ATACACTAATAAGAA[C/T]GTGTCAGAGCTCTTA | 5663 |
rs200164246 | snp | A/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219947 | CTTCTTCTCAAGCAC[A/T]GACACTCATTACCGT | 5663 |
rs200165137 | in-del | -/TCT | 0.0387552 | 0.1337 | intron-variant | PSEN1 | GRCh38.p7 | 14:73177292 | CCTTTGCATATCTCT[-/TCT]ACTCAGATACCTGGT | 5663 |
rs200170201 | snp | C/G | | | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137258 | CGATCTGCGGTGGTG[C/G]CAGAGGCTTACAAGA | 5663 |
rs200178809 | snp | A/C | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220328 | CAGCCCTGCTGTCAG[A/C]CCTTCTTCCACAGCA | 5663 |
rs200186908 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219500 | TGAACATACTTCATC[A/G]CAGTGGACTGTGTCC | 5663 |
rs200192050 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73173746 | GCTTTCCACCCTGTT[C/T]TTCTTATGGTTGGGT | 5663 |
rs200194433 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220057 | TTCAGTAAATTTTGG[A/G]AACAGTACAGCTATT | 5663 |
rs200198177 | in-del | -/A | 0.0517044 | 0.152246 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204387 | TGAAAAGTGATTTTT[-/A]AAAAAATATTATTTT | 5663 |
rs200203966 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73147810 | ACCTAATCTGGGAGC[C/T]TGCAAGTGACAACAG | 5663 |
rs200219842 | snp | A/G | 0.00170652 | 0.0291607 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206511 | ATCTTGATTTTTCAG[A/G]GTCACTGTTATAAGC | 5663 |
rs200258869 | in-del | -/T | 0.0126979 | 0.078662 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168516 | GGCTGAGCAGCGAGC[-/T]AGAGAATCAGGTGAG | 5663 |
rs200259626 | snp | A/C | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220213 | AAGCAGTCTTTTTCT[A/C]CAGCCAGTAAGGCAG | 5663 |
rs200327005 | snp | A/C | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219722 | CTACACGTTGAAAAT[A/C]AACCCAATAATTCTG | 5663 |
rs200342894 | in-del | -/TTTT | 0.35574 | 0.226537 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134533 | TTATTTATTTATTTA[-/TTTT]TATTTTTTGAGACAT | 5663 |
rs200357339 | in-del | -/CTT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73146862 | TATATTTCTGAAAAC[-/CTT]CTGTGAAAAGGAAGA | 5663 |
rs200372973 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219679 | TTAGGTGAAGTGGTT[G/T]AAACCAAACGGAACT | 5663 |
rs200373970 | snp | C/G | 6.59892e-05 | 0.00574371 | missense | PSEN1 | GRCh38.p7 | 14:73170854 | CTTGGCCACCCTGAG[C/G]CATTATCTAATGGAC | 5663 |
rs200376602 | snp | A/G | 6.75562e-05 | 0.0058115 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198002 | CCCATACATTTTATT[A/G]GATGTCTTTTATGTT | 5663 |
rs200378490 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73137031 | GCCTCTTGTTCGAGG[C/T]GGAAGACGGGGTCTG | 5663 |
rs200399921 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220191 | TCCTCATTCTTCTCT[C/T]CCACACAAGCAGTCT | 5663 |
rs200406138 | snp | C/T | 0.00122322 | 0.0247005 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173749 | TTCCACCCTGTTCTT[C/T]TTATGGTTGGGTATT | 5663 |
rs200423458 | snp | G/T | | | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136818 | GGGAGCCTTGGTCCG[G/T]AAATGCTGTTTGCTC | 5663 |
rs200435342 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219438 | AAGTCTTCCTGACCA[C/T]CTTGCACTATTGGAC | 5663 |
rs200464369 | snp | C/T | 1.64817e-05 | 0.00287064 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219298 | TATCTAGCATATTTG[C/T]GGTTAGAATCCCATG | 5663 |
rs200465950 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73171075 | TTTGTTTTATTATTC[G/T]CAAAGCCAGTGTGGC | 5663 |
rs200471959 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194420 | CACTACCATGCCTAA[-/T]TTTTTAAAAAAAAAT | 5663 |
rs200481721 | snp | C/T | | | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73198032 | TTTTCTTTTTCTAGA[C/T]TTAGTGGCTGTTTTG | 5663 |
rs200486703 | snp | C/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220356 | GCAAATGAGATGTAT[C/G]CCCAAAGACGGTAGA | 5663 |
rs200488046 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73173735 | CACAGATCTTTGCTT[C/T]CCACCCTGTTCTTCT | 5663 |
rs200493788 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73136852 | GACGTCTCAGGGCGC[A/G]GGTGCCTTGGGCCGG | 5663 |
rs200521615 | snp | G/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219480 | GTGCCTATAGAAAAC[G/T]ATTTTGAACATACTT | 5663 |
rs200523476 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73137063 | TGCTTTCTCCTTGGT[C/T]GGGACTGTCTCGAGG | 5663 |
rs200525059 | snp | A/G/T | 0.0099691 | 0.069894 | missense | PSEN1 | GRCh38.p7 | 14:73217230 | ACCATAGCCTGTTTC[A/G/T]TAGCCATATTAATTG | 5663 |
rs200531506 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73211758 | GCTGTAACTTCCACT[G/T]TCTCTTGAAGGCACA | 5663 |
rs200531676 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136493 | GGCAGCTCCGGGGTC[A/C]GCGGTTTCACATCGG | 5663 |
rs200538745 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73217316 | ACAGTCCCTTTAAGG[A/C]AGTTCTGTTTTAACC | 5663 |
rs200543953 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73199407 | TAGTGGAAAATTGGG[A/C]AAGCCAGTATTTTTC | 5663 |
rs200547750 | snp | C/G | | | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73219157 | CCTTACATTATTACT[C/G]CTTGCCATTTTCAAG | 5663 |
rs200576075 | snp | C/T | 0.00199802 | 0.0315439 | missense | PSEN1 | GRCh38.p7 | 14:73171031 | GTCAGCTTTTATACC[C/T]GGAAGGATGGGCAGC | 5663 |
rs200583938 | snp | A/G | | | utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73147842 | CTTTGCGGTCCTTAG[A/G]CAGCTTGGCCTGGAG | 5663 |
rs200597479 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73220421 | TCTGTCCTGGTATTT[G/T]GTTTTTGCTTTTGCC | 5663 |
rs200598249 | snp | A/C/G | 1.72985e-05 | 0.00294091 | missense | PSEN1 | GRCh38.p7 | 14:73148090 | ACAACCACCTGAGCA[A/C/G]TACTGTACGTAGCCA | 5663 |
rs200599205 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167743 | TCTGTTTTTTTTTTT[-/T]GTCTTCATTTCTGGT | 5663 |
rs200600659 | snp | A/G | | | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73170949 | GAAATATGGCGCCAA[A/G]CATGTGATCATGCTC | 5663 |
rs200601334 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220116 | CAAATTTGGATTTTC[C/T]ACCAAATTCTGAATT | 5663 |
rs200612813 | snp | A/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220254 | GTAGCAGATGGTCCC[A/T]TTATTCTAGGGTCTT | 5663 |
rs200622272 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73190910 | TTAATATAAATATCT[A/C]CATCGTCCAGAAATT | 5663 |
rs200629432 | snp | G/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219741 | CCAATAATTCTGTAT[G/T]AACTGAATTCTGAAC | 5663 |
rs200632899 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136539 | TGGTCTGGAAGGAAC[C/T]TGAGCTACGAGCCGC | 5663 |
rs200644664 | snp | A/G | | | missense | PSEN1 | GRCh38.p7 | 14:73219234 | TCTACTTTGCCACAG[A/G]TTATCTTGTACAGCC | 5663 |
rs200646139 | snp | A/G | 1.64961e-05 | 0.00287189 | missense | PSEN1 | GRCh38.p7 | 14:73171032 | TCAGCTTTTATACCC[A/G]GAAGGATGGGCAGCT | 5663 |
rs200659339 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73198164 | ATTGAATTAGTAATC[A/T]GTGTAGAATTTATCG | 5663 |
rs200692223 | snp | A/G/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219519 | TGGACTGTGTCCCTC[A/G/T]GTGCAGAAACTACCA | 5663 |
rs200698508 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136561 | ACGAGCCGCGGCGGC[A/G]GCGGGGCGGCGGGGA | 5663 |
rs200708784 | snp | C/G | 0.000528647 | 0.0162494 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148145 | GCCTTTGCCAGACTG[C/G]ATTCACTTATCATCT | 5663 |
rs200737712 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73147930 | TATAACAGTATAATT[C/G]TAGTGCACAAAGTTC | 5663 |
rs200746395 | in-del | -/G | 0.0345262 | 0.126772 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208046 | ACCTTGTGTTAACCT[-/G]GGGAACACAGGGGCA | 5663 |
rs200753166 | snp | G/T | 0.00021447 | 0.0103532 | missense | PSEN1 | GRCh38.p7 | 14:73211819 | AATGATGATGGCGGG[G/T]TCAGTGAGGAATGGG | 5663 |
rs200761597 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219926 | TGTAGATTGCCTTTG[A/G]CAATTCTTCTTCTCA | 5663 |
rs200768844 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219571 | GAGATATGATAGGCC[C/T]GGAAGTTGCTGTGCC | 5663 |
rs200808414 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73137150 | CCGTTGTGGTCAGCT[C/T]TGCTTTAGGCATATT | 5663 |
rs200809366 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73220443 | GCTTTTGCCACACAG[C/T]AGCTCAGAATTTGAA | 5663 |
rs200810527 | snp | A/G | 1.65919e-05 | 0.00288022 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211951 | GAGGAAAGTATGTGC[A/G]TTTCTCTATGTTGCA | 5663 |
rs200814320 | snp | C/T | | | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73186882 | GCTTATTATATCATC[C/T]CTATTGTTGCTGTTC | 5663 |
rs200818808 | snp | G/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220395 | AGAGTAAAATGGCTG[G/T]TGAAGCACTTTCTGT | 5663 |
rs200819835 | snp | G/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219840 | GTTCCAGCTTCCCTT[G/T]GATTTTTTGCTGCAG | 5663 |
rs200824179 | snp | A/G | 0.000431092 | 0.0146751 | missense | PSEN1 | GRCh38.p7 | 14:73170804 | GCTTATAGAATGACA[A/G]TAGAGAACGGCAGGA | 5663 |
rs200825897 | snp | C/G | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136417 | CCGTGGGCCGGCCGC[C/G]AACGACGCCAGAGCC | 5663 |
rs200836785 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220314 | TGAATCGGTGCTGTC[A/G]GCCCTGCTGTCAGAC | 5663 |
rs200863524 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73136976 | CGCCCCGGGTGTGTC[C/G]TTGTCCAGGGGCGAC | 5663 |
rs200875522 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73158336 | TATCTATCTATCTAT[C/T]TTTAAGACGGAGTTT | 5663 |
rs200884128 | snp | G/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73136930 | TCTTGGGCTGGGTCT[G/T]CTTGAGCAACTGGTG | 5663 |
rs200888596 | snp | G/T | 6.59207e-05 | 0.00574073 | missense | PSEN1 | GRCh38.p7 | 14:73211906 | GCTGTCCAGGAACTT[G/T]CCAGCAGTATCCTCG | 5663 |
rs200915258 | snp | A/G | 1.73528e-05 | 0.00294552 | missense | PSEN1 | GRCh38.p7 | 14:73198075 | CCACTTCGTATGCTG[A/G]TTGAAACAGCTCAGG | 5663 |
rs200924215 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73137206 | TGAGAGAATTGAGGT[A/G]ACTTTTCCATAATTC | 5663 |
rs200927187 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73136957 | GGTGAAACTCCGCGC[C/T]TCACGCCCCGGGTGT | 5663 |
rs200937800 | snp | G/T | 1.64727e-05 | 0.00286986 | missense | PSEN1 | GRCh38.p7 | 14:73173621 | CAGAGAGCCCTGCAC[G/T]CAATTCTGAATGCTG | 5663 |
rs200943013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136808 | AGAGATTCCGGGGAG[C/T]CTTGGTCCGGAAATG | 5663 |
rs200954466 | snp | A/C | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219434 | TTCCAAGTCTTCCTG[A/C]CCACCTTGCACTATT | 5663 |
rs200958188 | snp | A/G | 0.00156763 | 0.0279527 | missense | PSEN1 | GRCh38.p7 | 14:73170819 | ATAGAGAACGGCAGG[A/G]GCACAACGACAGACG | 5663 |
rs200974995 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173713 | GTGCTATAAGGTGAG[C/T]ATGAGACACAGATCT | 5663 |
rs200976865 | snp | G/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220331 | CCCTGCTGTCAGACC[G/T]TCTTCCACAGCAAAT | 5663 |
rs200984558 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220304 | GAATGTGTTATGAAT[C/T]GGTGCTGTCAGCCCT | 5663 |
rs200998182 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73182740 | GCTACTCGGGAGGCT[A/G]AGGCAGGAGAATTGC | 5663 |
rs201018520 | snp | A/G | 1.7688e-05 | 0.00297383 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206475 | TATAATGCAGAAAGT[A/G]GGTAACTTTTATTAG | 5663 |
rs201019113 | snp | A/C | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220040 | TAACCTCAGGTTCCA[A/C]ATTCAGTAAATTTTG | 5663 |
rs201019627 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73147761 | TTACTAGGATTTAAC[C/T]AACAATGGATGACCT | 5663 |
rs201037816 | snp | A/G | | | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73192824 | CAAGTACCTCCCTGA[A/G]TGGACTGCGTGGCTC | 5663 |
rs201051530 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73198003 | CCATACATTTTATTA[G/T]ATGTCTTTTATGTTT | 5663 |
rs201051937 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219687 | AGTGGTTTAAACCAA[A/G]CGGAACTCTTCATCT | 5663 |
rs201052276 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73157248 | CTCCTGCCTCAGCCT[C/T]CTGAGTAGCTGGGAT | 5663 |
rs201053733 | snp | G/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73137043 | AGGCGGAAGACGGGG[G/T]CTGATGCTTTCTCCT | 5663 |
rs201071856 | in-del | -/GGGAT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73174501 | CCAAAGTGCTGGGAT[-/GGGAT]TACAGGCATGAGCCA | 5663 |
rs201087233 | snp | A/C | 3.29484e-05 | 0.00405871 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73217217 | AGACTGGAACACAAC[A/C]ATAGCCTGTTTCGTA | 5663 |
rs201087568 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73136821 | AGCCTTGGTCCGGAA[A/G]TGCTGTTTGCTCGAA | 5663 |
rs201090176 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73213111 | TGAGTTTTCCAGATA[C/T]CAAAGCCCAGCTGCA | 5663 |
rs201091097 | snp | A/G | 5.77534e-05 | 0.00537339 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198179 | AGTGTAGAATTTATC[A/G]GAACTGAAGCACATG | 5663 |
rs201092260 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136449 | GAAATGACGACAACG[A/G]TGAGGGTTCTCGGGC | 5663 |
rs201103361 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219515 | GCAGTGGACTGTGTC[C/T]CTCGGTGCAGAAACT | 5663 |
rs201108356 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73136879 | CCGGGATTAGTAGCC[A/G/T]TCTGAACTGGAGTGG | 5663 |
rs201109862 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73165688 | AGGAAGCAGAGGCTG[G/T]GGTGAGCCGAGATCG | 5663 |
rs201113902 | snp | C/T | 4.94434e-05 | 0.00497184 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73170973 | CATGCTCTTTGTCCC[C/T]GTGACTCTCTGCATG | 5663 |
rs201118066 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73157125 | CCCTTGAGAAAGATA[-/T]CCTTTTTTTTTTTTT | 5663 |
rs201144186 | snp | C/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73137020 | GAAGTCCGCACGCCT[C/G]TTGTTCGAGGCGGAA | 5663 |
rs201187760 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73187942 | TGAAAAGAATAATAC[-/T]TTTTTTTTTTGAGTC | 5663 |
rs201216284 | snp | A/G | 0.000197902 | 0.00994545 | missense | PSEN1 | GRCh38.p7 | 14:73170870 | CATTATCTAATGGAC[A/G]ACCCCAGGGTAACTC | 5663 |
rs201219181 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219647 | TGCGAACTCTCAGGA[C/T]TACCGTTACCAAGAG | 5663 |
rs201227105 | snp | A/G | 3.29511e-05 | 0.00405887 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217251 | ATATTAATTGTAAGT[A/G]TACACTAATAAGAAT | 5663 |
rs201260629 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219398 | AAAGTCAAGATTCCC[A/G]GCTGGACTTTTGCAG | 5663 |
rs201263566 | snp | A/G | | | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136604 | TGATGGGGAGTCCGG[A/G]CAAGCCAGGAAGGCA | 5663 |
rs201270197 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73147882 | TGAAAGAAAGGTTTG[C/T]TTCTGCTTAATGTAA | 5663 |
rs201317432 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73177417 | TTGTTTTTGTTTTTG[-/T]TTTTGAGATAAAGTC | 5663 |
rs201322015 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73220404 | TGGCTGTTGAAGCAC[C/T]TTCTGTCCTGGTATT | 5663 |
rs201327731 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73137143 | CTTCTCACCGTTGTG[A/G]TCAGCTCTGCTTTAG | 5663 |
rs201339915 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73195961 | CCCAAGTCCAATATT[A/C]TTTTCACCGTATTAC | 5663 |
rs201355661 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220148 | GTAGACATACTTGTA[C/T]GCTCACTTGCCCCAG | 5663 |
rs201362083 | snp | C/T | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136402 | GGCTCCTCCCCTCCT[C/T]CGTGGGCCGGCCGCC | 5663 |
rs201362969 | in-del | -/TTATTTAT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73138192 | CTAATAAACATACTA[-/TTATTTAT]TTATTTATTTATTTA | 5663 |
rs201363471 | snp | C/T | | | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73173572 | TTATTGTAGAATCTA[C/T]ACCCCATTCACAGAA | 5663 |
rs201374878 | snp | C/T | 1.64806e-05 | 0.00287054 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73211908 | TGTCCAGGAACTTTC[C/T]AGCAGTATCCTCGCT | 5663 |
rs201375075 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220305 | AATGTGTTATGAATC[A/G]GTGCTGTCAGCCCTG | 5663 |
rs201375628 | snp | C/G | | | missense | PSEN1 | GRCh38.p7 | 14:73192687 | GTGGACTACATTACT[C/G]TTGCACTCCTGATCT | 5663 |
rs201383855 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220365 | ATGTATGCCCAAAGA[C/T]GGTAGAATTAAAGAA | 5663 |
rs201386708 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73148147 | CTTTGCCAGACTGGA[A/T]TCACTTATCATCTCC | 5663 |
rs201392519 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136480 | GGGGCCTGGGACAGG[C/G]AGCTCCGGGGTCCGC | 5663 |
rs201394035 | snp | C/T | 0.000104181 | 0.00721662 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206522 | TCAGGGTCACTGTTA[C/T]AAGCTAACAGTATAG | 5663 |
rs201412457 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73140202 | TCTTTTTTTGCTATT[C/T]TTTTTTTTTTTTTTT | 5663 |
rs201414759 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73158338 | TCTATCTATCTATTT[A/T]TAAGACGGAGTTTTG | 5663 |
rs201421129 | in-del | -/TGGGA | 0.0629771 | 0.165899 | intron-variant | PSEN1 | GRCh38.p7 | 14:73174500 | GGTCTCCCAAAGTGC[-/TGGGA]TGGGATTACAGGCAT | 5663 |
rs201430897 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136527 | CAAAACAGCGGCTGG[G/T]CTGGAAGGAACCTGA | 5663 |
rs201448807 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219546 | ACCAGATTTGAGGGA[C/T]GAGGTCAAGGAGATA | 5663 |
rs201452973 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219360 | GGGAGGACAAAGGTG[A/G]TTTTCCTGTGTCCAC | 5663 |
rs201453174 | snp | A/C/T | 8.23695e-05 | 0.00641707 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73219196 | GCCAGCTCTTCCAAT[A/C/T]TCCATCACCTTTGGG | 5663 |
rs201457009 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219736 | TCAACCCAATAATTC[C/T]GTATTAACTGAATTC | 5663 |
rs201496204 | snp | A/G | 0.000131794 | 0.00811661 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73219262 | GCCTTTTATGGACCA[A/G]TTAGCATTCCATCAA | 5663 |
rs201500006 | snp | C/T | 0.000132567 | 0.00814038 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73171046 | CGGAAGGATGGGCAG[C/T]TGTACGTATGAGTTT | 5663 |
rs201501112 | in-del | -/C | 0.0126979 | 0.078662 | intron-variant | PSEN1 | GRCh38.p7 | 14:73191558 | TTTTTTTTTTCTTTT[-/C]TTTTTTAGTTTTAGG | 5663 |
rs201501131 | in-del | -/T/TT | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73153676 | ATTTTTTTTTTTTTT[-/T/TT]GCCCATTAAGTCTTA | 5663 |
rs201506908 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73147832 | TGACAACAGCCTTTG[C/T]GGTCCTTAGACAGCT | 5663 |
rs201510690 | snp | A/G | 3.36491e-05 | 0.00410163 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211975 | TGTTGCAAAGTCATG[A/G]ATTCCTTTAGGTAGC | 5663 |
rs201513640 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220090 | TCATCAATTCTCTAT[C/T]ATGTTGAAGTCAAAT | 5663 |
rs201521677 | snp | A/C | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220318 | TCGGTGCTGTCAGCC[A/C]TGCTGTCAGACCTTC | 5663 |
rs201525609 | snp | G/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219825 | GAGAGGTGGGCAGGG[G/T]TTCCAGCTTCCCTTT | 5663 |
rs201552708 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136462 | CGGTGAGGGTTCTCG[C/G]GCGGGGCCTGGGACA | 5663 |
rs201571330 | in-del | -/AAGAAA | 0.00517822 | 0.0506191 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173475 | GATACGAATTGAATT[-/AAGAAA]AAGAAAATTCTGTGT | 5663 |
rs201572840 | in-del | -/CTC | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73177288 | TTCTCCTTTGCATAT[-/CTC]TTCTACTCAGATACC | 5663 |
rs201592313 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73136858 | TCAGGGCGCAGGTGC[C/T]TTGGGCCGGGATTAG | 5663 |
rs201593896 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167150 | GAGTATATGGTACCA[C/G]CAGCACCTGATTATG | 5663 |
rs201607577 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73197585 | AGTTCAGTCAAATCC[C/G]CTTTATTAAATTCAT | 5663 |
rs201612328 | snp | A/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219482 | GCCTATAGAAAACGA[A/T]TTTGAACATACTTCA | 5663 |
rs201613234 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136552 | ACCTGAGCTACGAGC[C/T]GCGGCGGCAGCGGGG | 5663 |
rs201617571 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73137095 | ATGCATGTCCAGTGA[C/T]TCTTGTGTTTGCTGC | 5663 |
rs201617677 | snp | G/T | 0.000131843 | 0.00811815 | missense | PSEN1 | GRCh38.p7 | 14:73173698 | TCTGTATAAATACAG[G/T]TGCTATAAGGTGAGC | 5663 |
rs201641438 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73186872 | TCCATGCCTGGCTTA[C/T]TATATCATCTCTATT | 5663 |
rs201644344 | snp | C/T | 8.23608e-05 | 0.00641667 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73173593 | ATTCACAGAAGATAC[C/T]GAGACTGTGGGCCAG | 5663 |
rs201653628 | snp | C/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73137152 | GTTGTGGTCAGCTCT[C/G]CTTTAGGCATATTAA | 5663 |
rs201663656 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73204314 | TTTTTTTTTTTTTTA[A/T]TTTAAACGAAATCTG | 5663 |
rs201664286 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219847 | CTTCCCTTTGATTTT[C/T]TGCTGCAGACTCATC | 5663 |
rs201690864 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136572 | CGGCAGCGGGGCGGC[A/G]GGGAAGCGTATGTGC | 5663 |
rs201709970 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73147766 | AGGATTTAACTAACA[A/G]TGGATGACCTGGTGA | 5663 |
rs201724748 | snp | C/T | 0.000116176 | 0.00762066 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192625 | TACATCTTTTAAAAT[C/T]TGTGTAATTTTTTTT | 5663 |
rs201726198 | snp | A/C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219603 | CATCAGCAGCTTGAC[A/C/G]CGTGGTCACAGGACG | 5663 |
rs201742793 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73137215 | TGAGGTGACTTTTCC[A/G]TAATTCAGGTGAGAT | 5663 |
rs201752111 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219946 | TCTTCTTCTCAAGCA[C/T]TGACACTCATTACCG | 5663 |
rs201759335 | snp | C/T | 4.97426e-05 | 0.00498686 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73170805 | CTTATAGAATGACAA[C/T]AGAGAACGGCAGGAG | 5663 |
rs201762901 | snp | C/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73136961 | AAACTCCGCGCCTCA[C/G]GCCCCGGGTGTGTCC | 5663 |
rs201775747 | snp | A/G | 3.68189e-05 | 0.00429046 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73198035 | TCTTTTTCTAGATTT[A/G]GTGGCTGTTTTGTGT | 5663 |
rs201776669 | snp | A/G | 0.00080687 | 0.0200695 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73211830 | CGGGTTCAGTGAGGA[A/G]TGGGAAGCCCAGAGG | 5663 |
rs201782907 | snp | C/T | 1.65132e-05 | 0.00287339 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173736 | ACAGATCTTTGCTTT[C/T]CACCCTGTTCTTCTT | 5663 |
rs201787759 | snp | C/T | 8.60089e-05 | 0.00655722 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206352 | CATACTTTGTGTGTC[C/T]AGTGCTTACCTGGAA | 5663 |
rs201788203 | snp | A/C | | | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137269 | GGTGGCAGAGGCTTA[A/C]AAGAAACACTAACGG | 5663 |
rs201789400 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219714 | ATCTTAAACTACACG[C/T]TGAAAATCAACCCAA | 5663 |
rs201790978 | snp | A/C | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73137050 | AGACGGGGTCTGATG[A/C]TTTCTCCTTGGTCGG | 5663 |
rs201813306 | snp | C/G/T | 6.85002e-05 | 0.00585196 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197993 | CAAGTTTAGCCCATA[C/G/T]ATTTTATTAGATGTC | 5663 |
rs201813672 | snp | A/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73137024 | TCCGCACGCCTCTTG[A/T]TCGAGGCGGAAGACG | 5663 |
rs201823720 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73204526 | AAAATGCTTTTTACA[A/T]TTAAAAAAAAAAAAA | 5663 |
rs201839481 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167847 | TTTTTTTTTTTTTTT[A/C]CTTCGAAGAATGATT | 5663 |
rs201868017 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73136939 | GGGTCTGCTTGAGCA[A/G]CTGGTGAAACTCCGC | 5663 |
rs201871244 | snp | C/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220046 | CAGGTTCCAAATTCA[C/G]TAAATTTTGGAAACA | 5663 |
rs201890140 | snp | A/G | | | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136791 | GGCGCGGCCGGGTGG[A/G]GAGAGATTCCGGGGA | 5663 |
rs201900780 | snp | C/T | 3.30622e-05 | 0.00406571 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73170826 | ACGGCAGGAGCACAA[C/T]GACAGACGGAGCCTT | 5663 |
rs201908084 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219408 | TTCCCGGCTGGACTT[C/T]TGCAGCTTCCTTCCA | 5663 |
rs201940545 | snp | A/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220291 | TGTATGATGAAAAGA[A/T]TGTGTTATGAATCGG | 5663 |
rs201945418 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73148093 | ACCACCTGAGCAATA[C/T]TGTACGTAGCCAGGT | 5663 |
rs201977851 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73186933 | GGGGTAAGTTGTGAA[A/G]TTTTTGGTCTGTCTT | 5663 |
rs201992645 | snp | A/T | 0.000126057 | 0.00793806 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198166 | TGAATTAGTAATCAG[A/T]GTAGAATTTATCGGA | 5663 |
rs201998552 | snp | C/T | | | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73170886 | ACCCCAGGGTAACTC[C/T]CGGCAGGTGGTGGAG | 5663 |
rs202004275 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136464 | GTGAGGGTTCTCGGG[C/T]GGGGCCTGGGACAGG | 5663 |
rs202021763 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73136848 | CGAAGACGTCTCAGG[A/G]CGCAGGTGCCTTGGG | 5663 |
rs202022163 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136453 | TGACGACAACGGTGA[A/G]GGTTCTCGGGCGGGG | 5663 |
rs202072789 | snp | A/G/T | | | utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73147833 | GACAACAGCCTTTGC[A/G/T]GTCCTTAGACAGCTT | 5663 |
rs202083888 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220096 | ATTCTCTATCATGTT[A/G]AAGTCAAATTTGGAT | 5663 |
rs202088076 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73174640 | GATATAATGGTCCCT[A/C]TAAAATACGGTATAA | 5663 |
rs202090424 | snp | C/T | 0.00199792 | 0.0315431 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73173662 | CAGTGTCATTGTTGT[C/T]ATGACTATCCTCCTG | 5663 |
rs202093573 | snp | G/T | | | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136810 | AGATTCCGGGGAGCC[G/T]TGGTCCGGAAATGCT | 5663 |
rs202094415 | snp | A/T | 1.69143e-05 | 0.00290807 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171068 | TATGAGTTTTGTTTT[A/T]TTATTCTCAAAGCCA | 5663 |
rs202109608 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219435 | TCCAAGTCTTCCTGA[C/T]CACCTTGCACTATTG | 5663 |
rs202123666 | in-del | -/TTAT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73138192 | CTAATAAACATACTA[-/TTAT]TTATTTATTTATTTA | 5663 |
rs202134342 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220380 | CGGTAGAATTAAAGA[A/G]GAGTAAAATGGCTGT | 5663 |
rs202164767 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73137000 | GGGCGACGAGCATTC[C/T]GGGCGAAGTCCGCAC | 5663 |
rs202172481 | in-del | -/ATTTATTTATTT | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134488 | AATTTATTGTACCAC[-/ATTTATTTATTT]ATTTATTTATTTATT | 5663 |
rs202175306 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73215542 | ACTTAAAAAAAAAAA[-/A]GGAAAATAAGCTACC | 5663 |
rs202176028 | snp | A/C | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219649 | CGAACTCTCAGGACT[A/C]CCGTTACCAAGAGGT | 5663 |
rs202195241 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219992 | TCTTCCCAAGGCCAG[C/T]CTGAACCTGAGGTTG | 5663 |
rs202198961 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73173714 | TGCTATAAGGTGAGC[A/G]TGAGACACAGATCTT | 5663 |
rs202199267 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220351 | CCACAGCAAATGAGA[C/T]GTATGCCCAAAGACG | 5663 |
rs202203280 | snp | G/T | 0.164546 | 0.234942 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154434 | ACGATCTTGTCTCTA[G/T]AAAAAAAAAAGTGAA | 5663 |
rs202209472 | snp | A/G | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136421 | GGGCCGGCCGCCAAC[A/G]ACGCCAGAGCCGGAA | 5663 |
rs202211178 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73211721 | ATTTTCTTAAAGGTA[C/T]TAAATTTTTCTAAAT | 5663 |
rs267606983 | snp | C/G | | | missense | PSEN1 | GRCh38.p7 | 14:73192744 | TCCATTCACTGGAAA[C/G]GTCCACTTCGACTCC | 5663 |
rs281875357 | multinucleotide-polymorphism | GC/TG | | | missense | PSEN1 | GRCh38.p7 | 14:73219185 | AAGAAAGCATTGCCA[GC/TG]TCTTCCAATCTCCAT | 5663 |
rs367775281 | snp | A/G/T | 9.90945e-05 | 0.00703841 | missense | PSEN1 | GRCh38.p7 | 14:73170834 | AGCACAACGACAGAC[A/G/T]GAGCCTTGGCCACCC | 5663 |
rs367800884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201244 | AGGCACACGCCGCCA[C/T]GCCCGGCTAATTTTT | 5663 |
rs367820243 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73168287 | TTGAACCTGGGCGGC[A/G]GAGGTTACAGTGAGC | 5663 |
rs367826892 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222390 | TTATTACTTGTTATT[C/T]ACGTGGCCTCAGACA | 5663 |
rs367896299 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193198 | ACCTGTAGTTCCAGC[C/T]ACTTAGGAGGCTGAG | 5663 |
rs367901180 | in-del | -/CCT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73193901 | GGCTCAAGCAATCCT[-/CCT]ACCTTGGCCTCTCAA | 5663 |
rs367937261 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220077 | GTACAGCTATTTCTC[A/G]TCAATTCTCTATCAT | 5663 |
rs367946310 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209957 | ACCCACTAAATGCCA[A/G]TAATGGCTTTAAGGC | 5663 |
rs367954742 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73157288 | GCACCACCACACCCA[G/T]CTAATTTTTTTGTAT | 5663 |
rs367954967 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222669 | AGAAAACAAGAGATT[A/G]TAACTACATTCTGAG | 5663 |
rs367957067 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73138402 | TTTTTTGTATTTTTA[G/T]TAGACACGGGGTTTC | 5663 |
rs367964042 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73168598 | AGAATAGGCCCAGCC[A/G]GAGATGGCCTGGCTT | 5663 |
rs367986036 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73215242 | CTGGGATTACAGGTG[G/T]GAGCCACTGTGCCCG | 5663 |
rs367996212 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73187040 | TAATTGTTTCCACAT[A/G]TAGGTCATACTTGGT | 5663 |
rs368006623 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73143732 | TCTTTTAAAATGACC[A/G]GTGGCTGCAGTGGCT | 5663 |
rs368033780 | in-del | -/TTTG | 0.222381 | 0.24847 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201076 | AAAAGAGAATATCTT[-/TTTG]TTTGTTTGTTTGTTT | 5663 |
rs368080237 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197176 | CTGACCTTGTGATCC[A/G]CCCACCTCGGCCTCC | 5663 |
rs368081586 | snp | C/T | 6.68159e-05 | 0.00577957 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211962 | GTGCATTTCTCTATG[C/T]TGCAAAGTCATGGAT | 5663 |
rs368122537 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73206076 | TCAACTAGTCCAGCT[A/G]TTGTTTCAGTGGAAT | 5663 |
rs368170929 | snp | A/G | 0.000131846 | 0.00811822 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219299 | ATCTAGCATATTTGC[A/G]GTTAGAATCCCATGG | 5663 |
rs368187678 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73188221 | GCCTGAGCCACCGCA[C/T]CCTGCCATAATAATA | 5663 |
rs368271347 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73198838 | GAGTACAGTAGTGTG[A/G]TCATGGCTCACTGCA | 5663 |
rs368301116 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73199966 | TGACCAGGCTGGTCT[C/T]GAACTCCTGACTTCA | 5663 |
rs368329004 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221397 | ATTTATTTGTGTAAG[A/G]ATCCCAAATGTGTTG | 5663 |
rs368422748 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197308 | GTGGTATAAACAGGA[A/G]TAACAGGCATGTTGT | 5663 |
rs368437028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73174529 | ATGAGCCACTGCGCC[C/T]GGCCCTAAGTGGTTT | 5663 |
rs368482128 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73186122 | GTGCGGTGGCAACCT[A/G]TAATCCTAGCACTTT | 5663 |
rs368499173 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73142307 | AAATCACAAGCTCAT[C/T]GGCACTTGAAACTTA | 5663 |
rs368520145 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73198436 | CCTTTGAGTGACTGG[C/T]TTAGATGTCTTTCTG | 5663 |
rs368562320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148848 | TGAGCCAGGAGAATC[A/G]CTGGAACCCAGGAGG | 5663 |
rs368575250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162815 | TTGTATTTGCTTGCA[C/T]ATGTAGAAAGAAACT | 5663 |
rs368643965 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200825 | GGAGGCCTAGGTGGG[C/T]GGATCACTTGAGGTC | 5663 |
rs368768865 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73149796 | GTTGACATTGTTGTT[C/T]AACTTCGAGTACTAT | 5663 |
rs368830324 | snp | C/T | 3.29544e-05 | 0.00405908 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73211893 | TGAGTCACGAGCTGC[C/T]GTCCAGGAACTTTCC | 5663 |
rs368867688 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73205794 | AAAATGTGGTAGAGA[C/T]GCACATGTGTATATC | 5663 |
rs368908264 | snp | A/G | 1.64917e-05 | 0.00287151 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73192650 | TTTTTTCAGGGAAGT[A/G]TTTAAAACCTATAAC | 5663 |
rs368913315 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73207710 | CTGAGATTTGCTCAG[C/G]CCCACTGGGCTCATT | 5663 |
rs368921134 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73165743 | ACAAGAGTGAAACTC[C/T]GTCTTAAAAAAAAAA | 5663 |
rs368943066 | in-del | -/TGCT | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179845 | TCTTTTGCAACCAGC[-/TGCT]TGCTGCCTGCTTTCT | 5663 |
rs368987122 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73198946 | GCCTGGCTAATTTTT[C/T]TGTGTTGTGTGTAGA | 5663 |
rs369020581 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73212142 | TTTGAGACAGAGTCT[C/T]GCTCTGTCGCCAGGT | 5663 |
rs369050931 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201311 | CAGGATGGTCTCGAT[C/T]TCCTGACCTTGTGAT | 5663 |
rs369075999 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PSEN1 | GRCh38.p7 | 14:73182817 | GCACTCCAGCCTGGG[C/T]GACAAAGTGAGGCTT | 5663 |
rs369084415 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73150851 | GAGGAGGGCGGATCA[C/T]GAGGTCAAGAGACAG | 5663 |
rs369089435 | in-del | -/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73140188 | AACTAAAAGGTTTTT[-/C]TTTTTTTGCTATTCT | 5663 |
rs369102324 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192914 | GAATGCCCCACTGGA[C/G]TGTTTTCTTTCCTCA | 5663 |
rs369122709 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139567 | ACTGGGCTACAGAGC[A/G]AGACTCCATAAGAAA | 5663 |
rs369127262 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73216046 | CAAATTGAAAACAAT[C/T]CAGATGTCCATCAAC | 5663 |
rs369131111 | snp | A/G | 0.000461893 | 0.0151899 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186839 | TAATTATATTGAAAT[A/G]CTTTCTTTTCTAGGT | 5663 |
rs369148418 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73212260 | GGACTACAGGCGTGC[A/G]CCACCACGCCTGGAT | 5663 |
rs369169349 | in-del | -/GA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73162644 | CAGCCTAGTGACAGA[-/GA]ATCTGTCTCAAAGAT | 5663 |
rs369279041 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73205352 | GGCATGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT | 5663 |
rs369457786 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73212233 | CTCCTGCCTCAGCCT[A/C]CCAAGTAGCTGGGAC | 5663 |
rs369503109 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PSEN1 | GRCh38.p7 | 14:73159676 | AGTCATGGGTCAAAG[A/G]CTGTTCTCATGGGGA | 5663 |
rs369531201 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194143 | AGCTTTCAGGTACGT[A/C]CTCTGTGGCTGTTGC | 5663 |
rs369540718 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223384 | ATTTCCCAGAAAGCA[A/G]TTTTCCTTTTGAAAT | 5663 |
rs369648040 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73196973 | AGTCTCGCTGTATTG[C/T]CCAGGCTGGAGTGCA | 5663 |
rs369654241 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156493 | TTTATGAAGGAAATG[A/T]TATATCTAAGATTTG | 5663 |
rs369657165 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73199515 | TGGTGGGTATCCTCA[C/T]TGATAGACATTTAGA | 5663 |
rs369663854 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167772 | TTCATTTCTGGTGGG[G/T]TTGGATAAGAAAAGT | 5663 |
rs369675790 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73177165 | TTTTTCGTCTCTCCC[A/G]TTACTTCTTGGGAAA | 5663 |
rs369724140 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145955 | CTACTAAAAATACAA[A/G]AATTAGCTGGACATG | 5663 |
rs369737143 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73175079 | TAATCCCAGCACTTT[A/G]GGAGGCCAAGGCAGG | 5663 |
rs369744477 | snp | C/T | 1.6585e-05 | 0.00287962 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211950 | AGAGGAAAGTATGTG[C/T]ATTTCTCTATGTTGC | 5663 |
rs369750792 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73183826 | GGCACACCTCCCAGA[C/T]GGGGTGGTGGCCGGG | 5663 |
rs369765449 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210502 | GTTATGGCACAATGA[A/G]CATGCTACTTATAAT | 5663 |
rs369767425 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73207110 | TCACTTGAGCTAAGG[A/T]GTTCCGGATTACCCT | 5663 |
rs369880711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73164375 | TTTATATGCAGTTTC[A/G]TCTGGACAATACCCT | 5663 |
rs369914882 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73160839 | TTGAGATGGAGTCTC[G/T]CTCTGTCGCCCATCC | 5663 |
rs369995753 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154592 | GGCAGCAAAGTGAGA[A/C]CCTGCCTCAAAAAAA | 5663 |
rs370225053 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73160474 | TTTTGAGGAACCTCC[A/G]TATTGTTTTCCATGG | 5663 |
rs370229001 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73203632 | CAGTTTGCAAAATGC[C/T]CTTACTGACAGGAAA | 5663 |
rs370229040 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73141764 | CATTCCAGCCTGGGC[A/G]ACAAGAGTGAAACTA | 5663 |
rs370231392 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73215776 | TAATCAGAGTGGCTA[A/G]AATGAAAAAGGCTAA | 5663 |
rs370273229 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73184992 | GGCAGAGGCGCTCCC[C/T]ACATCTCAGACGATG | 5663 |
rs370315616 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | PSEN1 | GRCh38.p7 | 14:73161729 | TGGTGTCCGGGTCAC[A/T]CATGGCTGACCTCAG | 5663 |
rs370352758 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197005 | TGGCGCAATCTCGGC[G/T]CACTGCAAGCTCCGC | 5663 |
rs370487918 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73153681 | TTTTTTTTTTTGCCC[A/C]TTAAGTCTTAAAGGA | 5663 |
rs370528248 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222135 | GTTCTCAGTAGGTTC[A/G]TGTGTGTTCCTAGAA | 5663 |
rs370623087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143482 | TGAGTTTTTTTTTAC[A/G]TGTCAGTACAGATTC | 5663 |
rs370673457 | in-del | -/ATTT | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134488 | AATTTATTGTACCAC[-/ATTT]ATTTATTTATTTATT | 5663 |
rs370699052 | in-del | -/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73146184 | CTAGTTTTAAAAAAT[-/C]TTTTTTTTTTTTTTT | 5663 |
rs370754072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162615 | GGTAAGCTGTTGACT[A/G]TGCCACTGCACTGCA | 5663 |
rs370786580 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73200438 | CCACGCCTGGCTGAT[C/T]TTTGTATTTTTAGTA | 5663 |
rs370900918 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73147614 | TTTGGTGTCTCAGGC[A/G]GTTCTACTTATTGCT | 5663 |
rs370939265 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212612 | GTACATTATTATTCC[G/T]TTTGTTGACAAGTGC | 5663 |
rs370947651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73172231 | TAGTTCCATCTCTAC[A/G]ACTCTCATGGGGTCC | 5663 |
rs370951231 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73151934 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 5663 |
rs370972528 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73178490 | ACCATGCCTGGCTCT[C/T]TACCCTCTTCTGGGA | 5663 |
rs370996267 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73168651 | ATACCATCCCTTTTT[-/T]CAACTCCCCATTCTG | 5663 |
rs371011840 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217253 | ATTAATTGTAAGTAT[A/C]CACTAATAAGAATGT | 5663 |
rs371102043 | snp | A/G | 3.3012e-05 | 0.00406262 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219328 | GGATGTTTCTTCTTT[A/G]ACTATAACAAAATCT | 5663 |
rs371112119 | snp | C/T | 3.31785e-05 | 0.00407286 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73148034 | AATGACAGAGTTACC[C/T]GCACCGTTGTCCTAC | 5663 |
rs371182331 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73178777 | CCCTTACTTCTTGGA[C/G]CATTTTTATGCTCCA | 5663 |
rs371208067 | in-del | -/TCATT | 0.00119737 | 0.0244387 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221296 | CTAGCATGGGTATTA[-/TCATT]GAGAAAGCACAGCTA | 5663 |
rs371274554 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSEN1 | GRCh38.p7 | 14:73165860 | CAGGAGTTCGAGACC[A/G]GCCTGGCCAACATGG | 5663 |
rs371377351 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73199869 | TCCTGCCTCAGCCTC[C/T]GGAGTGGCTGGGATT | 5663 |
rs371435042 | snp | A/G | 0.000178301 | 0.00944026 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208905 | TGCCAAAGGGTGCCT[A/G]CAGGCCCACGGTAAG | 5663 |
rs371437655 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73154853 | TAAAAATTAAAACTT[C/T]ACTTCTTACCTATCA | 5663 |
rs371489327 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145283 | GCTTTGCTTCTGAGG[G/T]ATTATATGAGAGTTC | 5663 |
rs371540312 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | PSEN1 | GRCh38.p7 | 14:73182371 | GGTGGTGTACCCACG[A/C]CTATAGTCCTAGGTA | 5663 |
rs371552722 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158365 | TTTGCTCCATCTGGA[A/G]CAAAGGCTGGAGTGC | 5663 |
rs371556256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73191538 | TTCCAAAATACGTAC[A/G]TATATTTTTTTTTTC | 5663 |
rs371559217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151855 | ATTACAGGTGTGAGC[C/T]ACTGCGCCCAACCTA | 5663 |
rs371559631 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209459 | TGAGCATGTAGGTAT[A/T]TATGTATGTGAGTGA | 5663 |
rs371580884 | multinucleotide-polymorphism | CC/TT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73151512 | TGATCTTGGTGATTT[CC/TT]CCCTTTCATTTTCTA | 5663 |
rs371588222 | in-del | -/GA | 0.302826 | 0.244355 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162474 | TCTCTCCATGAGAAG[-/GA]GAGAGAGAGAGAGAG | 5663 |
rs371718090 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222488 | AGGGTTAGATGACTG[C/T]GGGAAGCCTTTGATC | 5663 |
rs371755869 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73149257 | AGGAACTCAGGAGGC[C/T]GAGGTACGAGGATTG | 5663 |
rs371765981 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73140532 | TTATAACTAATTTAA[A/C]AGCAAAATCTGGCCT | 5663 |
rs371847680 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73174296 | TGAAGTGCAGTGGCA[C/T]GATTTTGGCTCACTG | 5663 |
rs371858400 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSEN1 | GRCh38.p7 | 14:73215283 | TTTTTTTTAAATACC[A/G]TTAAGAAGTGGAAAA | 5663 |
rs371870381 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73174608 | ATGAATCTCCTCATT[C/T]ACAAATAACACTGTA | 5663 |
rs371951157 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205066 | GGTGGTCGTTCAGCT[G/T]CTTTGATTGTGTGTT | 5663 |
rs371982343 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73138689 | AAAAAGGCCGAGCGC[A/G]GTGGCTCACCCCTGT | 5663 |
rs371983982 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73163722 | GTCAGGTGGGAGAAG[G/T]GCATTCCAGATGAAC | 5663 |
rs372038674 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73149803 | TTGTTGTTTAACTTC[A/G]AGTACTATTACAGTT | 5663 |
rs372072966 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73188228 | CCACCGCACCCTGCC[A/G]TAATAATACATTTGA | 5663 |
rs372207900 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73163353 | GAGGCCAAGGCAGGA[A/G]GATTGCTTGAGCCCA | 5663 |
rs372234096 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193874 | ATTGCCTAGGCTGGT[-/C]TTGAACTCTTGGGCT | 5663 |
rs372245637 | in-del | -/AAGAATGCTCCCGCACAGCATA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73218653 | CTCCCACACAGCATA[-/AAGAATGCTCCCGCACAGCATA]GAGAATGCCCCCGCA | 5663 |
rs372248761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145657 | ATGCAATTTATTGAC[C/T]ACTTCACTGAAAGTG | 5663 |
rs372322502 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73180884 | CAAGATTAGTCTTTT[A/T]TGTCAAGTAACTAAG | 5663 |
rs372333965 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73170191 | CTTGGTTTTGGTGGG[-/T]TTTGGCCAGCTTCTT | 5663 |
rs372349684 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73187813 | AATTTTATGAAGCCA[C/G]CATAACATTAATAAC | 5663 |
rs372357057 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194681 | TCATGCCGTTCTCCT[A/G]CCTCAGCCTCCCAAG | 5663 |
rs372358531 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73169610 | ATTCATTGCCACTCA[A/G]TCAAGTTTGCTAAAA | 5663 |
rs372414758 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73179478 | AAAATTAGCCAGGCA[-/A]TGGTGGTGGGCACCT | 5663 |
rs372423679 | in-del | -/GTA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73180810 | TGTGTGTATAACATA[-/GTA]ATAAAAGAAATGCAT | 5663 |
rs372427463 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222134 | GGTTCTCAGTAGGTT[C/T]GTGTGTGTTCCTAGA | 5663 |
rs372430923 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73185011 | TCTCAGACGATGGGC[A/G]GCCGGGCAGAGACGC | 5663 |
rs372434939 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73160695 | GAGCATCTTTTCATG[C/T]GCTTGTTGGCTATTT | 5663 |
rs372439319 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73141770 | AGCCTGGGCGACAAG[A/T]GTGAAACTACATCTT | 5663 |
rs372523987 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73170669 | TGCATACTTCCTGTA[C/G]ATTGTTTTTTCTTGC | 5663 |
rs372539617 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73165331 | TCTCACTACATTCCC[C/T]GGCTCAAACGATTCT | 5663 |
rs372541398 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73188268 | GTTTGTTTGCAGAAT[C/T]GTTCATTATAAGTTG | 5663 |
rs372551103 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73146554 | ACATGGTACATAAAA[A/G]CATGTATGATAAAGT | 5663 |
rs372660395 | in-del | -/GCA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167153 | TATATGGTACCAGCA[-/GCA]CCTGATTATGCCATG | 5663 |
rs372716222 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73193550 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAG | 5663 |
rs372764513 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73197894 | TGCCATTTATTTCAT[A/T]TTCATTCAACGTCTT | 5663 |
rs372871130 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73175586 | GTGTAATCAATATGT[A/G]TCCTTTTACTTTGGT | 5663 |
rs372925839 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73200901 | ACTAAAAATATAAAA[A/G]TCAGCTGGGTGTGGT | 5663 |
rs372933281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157671 | CCATGTTTTGTCACC[A/G]CGCGCAGCCATTTAC | 5663 |
rs372935430 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73189181 | AAGAAATACGAACTA[C/T]ATAATTTGGAAAAGA | 5663 |
rs373003664 | snp | C/T | 0.0528381 | 0.153711 | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73223929 | GGCGACAGAGCAAGA[C/T]TCTGTCTCAAAAAAA | 5663 |
rs373009033 | in-del | -/AGC | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73144028 | AAAGATTTGCATTAT[-/AGC]TTATCTTTTTTTTTT | 5663 |
rs373075170 | in-del | -/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73140202 | TCTTTTTTTGCTATT[-/C]TTTTTTTTTTTTTTT | 5663 |
rs373105605 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168122 | GCACTTTGGGAGACC[A/G]AGGCAGGTGGATCAC | 5663 |
rs373248333 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217741 | CCATGCATGACCCCA[C/T]ATAGATCTTGCTGAT | 5663 |
rs373319061 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73201851 | TCCCAAGTTCAAGCA[A/G]TGGTCCTGTCTCAGC | 5663 |
rs373410370 | in-del | -/C | 0.00517822 | 0.0506191 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135988 | AGAAAGACTGGTTGT[-/C]AAAGTTGGAGTCCAA | 5663 |
rs373410824 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186963 | TTCAGAATTAACTAC[A/C]TTTGTGCTGTGTAGC | 5663 |
rs373424819 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73200027 | GCCAGGATTATAGCT[A/G]TGAGCCACCATGCCC | 5663 |
rs373483727 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200777 | GGAGAGAGGCTGGGC[A/G]TGGTGGCTAACACCT | 5663 |
rs373513040 | in-del | -/GTT | 0.00358779 | 0.0422022 | intron-variant | PSEN1 | GRCh38.p7 | 14:73155716 | TAGAGCTGGGGTCTC[-/GTT]ATGTTGCCCAGGCCG | 5663 |
rs373522479 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73184769 | CACCTCCCTCCCGGA[C/T]GGGGTGGCTGCCGGG | 5663 |
rs373536018 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73141485 | TTAAATTAGTTTAAA[A/C]ATTTTTTTTATTAAT | 5663 |
rs373544899 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73182301 | CTTGGGCAACAGAGT[C/G]AGACCCCCACCTCTA | 5663 |
rs373580421 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73155845 | TCATGGAAACCTGTC[A/C]TTATCTGTTTATACA | 5663 |
rs373588204 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173929 | CTGAGGCAGGAGGAT[C/T]ACTTGGGCCCAGGAG | 5663 |
rs373600610 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73146038 | CTTAAACCCAGGAGT[C/T]AGAGGTTCCAGTGAG | 5663 |
rs373628918 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162687 | GGATATTCTTTATGT[A/T]CTGATGTGTAGAAAA | 5663 |
rs373648722 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73160789 | TGTTTTTTTCCAATT[G/T]TTTAATTGTAGGACT | 5663 |
rs373665430 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73140878 | AACTCAGCAGTTCAG[A/G]GCATGTATTCTCACT | 5663 |
rs373672675 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73210403 | AAGACAGGAAGAGTT[-/A]ACATTTGCGTGCACT | 5663 |
rs373743373 | in-del | GG/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73216069 | CCATCAACTGGTAAA[GG/T]GGATAAGCAAACCAT | 5663 |
rs373744985 | in-del | -/GC | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73193565 | AAAAAAAAAAAAAAA[-/GC]AAAAAAAAAAAAGCA | 5663 |
rs373752770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212259 | GGGACTACAGGCGTG[C/T]GCCACCACGCCTGGA | 5663 |
rs373808154 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73146184 | CTAGTTTTAAAAAAT[C/T]TTTTTTTTTTTTTTT | 5663 |
rs373894154 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217714 | GCAAGCATCTAGTGA[C/G]AGGAGCTGGTGCCAT | 5663 |
rs373992281 | snp | C/T | 1.64784e-05 | 0.00287035 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73219286 | CCATCAATTTTATAT[C/T]TAGCATATTTGCGGT | 5663 |
rs373997886 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73138821 | AAAAAAAAAAAATTA[G/T]CCGGGCGTGATGGCG | 5663 |
rs374005545 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73153917 | TGGGGTTTCACCATG[C/T]TGGTCAGGCTGGTCT | 5663 |
rs374005824 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73204339 | AATCTGCTTATTTTC[C/T]TGTTGATGTAAGGTG | 5663 |
rs374012398 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73185840 | AGGCATGAGTCACTG[C/T]GCCCGATCTCTCAGT | 5663 |
rs374033381 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73202816 | GTCTGTGCTCGCTTT[A/C]GCAGCACATAATAGT | 5663 |
rs374039699 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73199777 | TGGAGACTGAGTCTC[A/G]CTCTGTCATGCAGGC | 5663 |
rs374047525 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73191912 | TGTCCTAGCTATAAA[A/G]TTTGTTAGCACATGT | 5663 |
rs374053908 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73177717 | CTTTCAGCCTCCATG[C/G]TTTCTCATAAAAATC | 5663 |
rs374061412 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219960 | ACTGACACTCATTAC[C/T]GTCTGTGATTGCCAT | 5663 |
rs374072277 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156031 | AGTTTTGCTGTGGAT[C/T]TAAGTTTGCATTTAA | 5663 |
rs374072714 | in-del | -/TT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73177976 | TTACTCTTTTTTTTT[-/TT]GAAACAGAGTGGCGC | 5663 |
rs374073959 | snp | G/T | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135471 | CTCACGGGTTCAAGC[G/T]ATTCTCCTGCTGCAG | 5663 |
rs374082928 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73180511 | AACCCTGAGGATTTT[C/T]CATATCAGTGGTTGG | 5663 |
rs374086244 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73164325 | ATTCCATAGTGCCGA[C/T]GATTTTCTATTGATA | 5663 |
rs374092535 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73195588 | AGAACAATGTCTATC[A/C]GTAAATTTTTTTCTG | 5663 |
rs374096090 | snp | A/T | | | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73138037 | AGATTATGCCACTGC[A/T]CTGCAGCCTGGGCAA | 5663 |
rs374118745 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73178872 | TCAAAGCCTTTGCAG[C/T]GTTGCTCAGATCTGC | 5663 |
rs374155053 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73200618 | AGGATAAACATTACA[G/T]ATAAAAATAAATTTC | 5663 |
rs374155429 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73197018 | GCGCACTGCAAGCTC[C/T]GCTTCCCGGGTTCAC | 5663 |
rs374161910 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73151336 | AGTCTGTGTGCACTT[C/G]TGTGAGTTTCTCAAA | 5663 |
rs374165145 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73208350 | TGAAAAGGTGCTTTA[C/T]TGAGCAACAGTACAG | 5663 |
rs374165198 | in-del | -/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73144065 | TTTTTTTTGAGATGG[-/G]AGTCTCACTCTGTCA | 5663 |
rs374167415 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73159411 | AACTTTGGCCTACTT[A/C]AAGTTCTCAGGAGTT | 5663 |
rs374168443 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73183391 | TGGAGGGAAGGTCAG[C/T]AGATAAACAAGTGAA | 5663 |
rs374169411 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73157431 | GGCGTGAGTCACCAC[A/G]CCCAGCCCAAGAAAG | 5663 |
rs374179523 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73153070 | AATACATAGACAAAA[A/T]GCAAACCTATGAGCT | 5663 |
rs374184263 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73165920 | CATTAAGCCGGCGCA[A/G]TGGTGGATGCCGATA | 5663 |
rs374276284 | snp | A/G | 2.54547e-05 | 0.00356745 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198167 | GAATTAGTAATCAGT[A/G]TAGAATTTATCGGAA | 5663 |
rs374520741 | snp | A/G | 3.30306e-05 | 0.00406377 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186972 | AACTACCTTTGTGCT[A/G]TGTAGCTATCATTTA | 5663 |
rs374546705 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222291 | GAGGCAGTGTTTTTA[C/T]TTTCAGACTCCGGGA | 5663 |
rs374615740 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73218923 | AGGGATAAAATAACA[A/G]TGTGTGCATAATGAA | 5663 |
rs374649890 | in-del | -/C | 0.0221141 | 0.102801 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179803 | CTAGTACTTCTAATT[-/C]CCCAGCCCACCTACC | 5663 |
rs374700409 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73142434 | AGCCCTTTGTGCTAG[A/G]GATCATGGTTAAAAG | 5663 |
rs374705731 | in-del | -/ATTC | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73140199 | TTTTCTTTTTTTGCT[-/ATTC]TTTTTTTTTTTTTTT | 5663 |
rs374741068 | snp | A/G | | | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137682 | AGGGTCGCCAGAGCT[A/G]AGGAAGGGGAGGGAA | 5663 |
rs374781022 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73175439 | CCGAGGTCAGGGGTT[G/T]GAGACCAGCCTGAGC | 5663 |
rs374805610 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217278 | GAATGTGTCAGAGCT[C/T]TTAATGTCAAAACTT | 5663 |
rs374865202 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168556 | CTATGGATGGGACGT[G/T]GCTAACTTCAGATGG | 5663 |
rs374871200 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73200332 | TGGAGTACAGTGGCG[C/T]AATCTCAACTCACTG | 5663 |
rs374891121 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73202438 | TATATATATATATAT[A/T]TATATATATATATAT | 5663 |
rs374964495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154051 | ATTATTGAAAAAATG[C/T]ATTTTAAGTAAATAT | 5663 |
rs375056492 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73148792 | ACAAAAATTAGCCGG[C/G]CTTGGTGGCAGGTGC | 5663 |
rs375096624 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73215851 | ATTGTTGCTGGTGGA[A/G]ATTCAGACTGGTACA | 5663 |
rs375314975 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222602 | TGTTCAGTGTTTTCT[A/G]TGTTCCCGTAGGTTC | 5663 |
rs375376095 | snp | A/G | 6.59935e-05 | 0.0057439 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173724 | TGAGCATGAGACACA[A/G]ATCTTTGCTTTCCAC | 5663 |
rs375383291 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73169709 | CACCCATAGTGGCAC[C/G]ATCTCTGCTCACTGC | 5663 |
rs375419545 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73166620 | GGCAGATGACTTAGT[A/C]ACCTCCTTCTGTGGA | 5663 |
rs375420006 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73140895 | CATGTATTCTCACTC[A/G]GGGCTCTGCTTCCTT | 5663 |
rs375489593 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73174876 | TCTCCTCCCCTAGCT[C/T]GCTCTTTTGCCAAAG | 5663 |
rs375590666 | snp | A/G | 3.295e-05 | 0.00405881 | intron-variant | PSEN1 | GRCh38.p7 | 14:73219108 | TAATTATGTGTGAAT[A/G]TGTGTCTTTCCCATC | 5663 |
rs375593838 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73204609 | CCATTTACAGAAAAA[G/T]TTAGCTGGACATTGA | 5663 |
rs375610238 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162647 | CCTAGTGACAGAGAA[A/T]CTGTCTCAAAGATAA | 5663 |
rs375724267 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73153949 | GAACTCCTGACCTCA[A/C]GTGATCTGACCACCT | 5663 |
rs375819380 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73165706 | TGAGCCGAGATCGCA[C/T]CATTGCACTCCAGCC | 5663 |
rs375837203 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157779 | GGAGGTCGAGGTGGG[C/T]GATGACTTGAGGCCA | 5663 |
rs375912087 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | PSEN1 | GRCh38.p7 | 14:73188009 | TCTCGGCTCACTGCA[A/G]CCCCCACCTCCTGGA | 5663 |
rs375987607 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73204172 | CCGGGCTAATTTTGT[A/G]TTTTTAGTAGAGACA | 5663 |
rs376000184 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73185098 | GGGATGGCGGCCGGG[C/T]GGAGACGCTCCTCAC | 5663 |
rs376000642 | in-del | -/CTGT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209441 | AAATCAAATGATTGT[-/CTGT]GAGCATGTAGGTATA | 5663 |
rs376050447 | snp | C/T | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134848 | TACCATATTTAGTTT[C/T]CCAATTTTTTGCTAT | 5663 |
rs376071858 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73187479 | GGCAGTCAAACTAAT[A/G]AATAAATTGGAGAGT | 5663 |
rs376093562 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209241 | GTTCCTGGCTCCTGC[C/T]AGCTCACAGAGCATG | 5663 |
rs376100145 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73191374 | GTGTATTAAAAAATG[C/T]ATTTGTATATATGTG | 5663 |
rs376100443 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73166189 | TCAGCCTTGGGCAGG[G/T]CAGGGTTGAGTTGGC | 5663 |
rs376105993 | snp | A/G | | | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73224177 | GTACAGTGCAGATAT[A/G]TGCTGGAGGATTTTT | 5663 |
rs376196437 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136673 | TGTGGCCGCCCGGGC[C/T]GCGAAGCCGGTGTCC | 5663 |
rs376241733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73161609 | AGGCTCAAGCTGTCA[A/G]TAGTCCTCTCCCAGT | 5663 |
rs376307406 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73159429 | GTTCTCAGGAGTTTT[C/T]TCCTGCATTTTCTTC | 5663 |
rs376316327 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73179233 | TCCAGTCAGAGTAAG[A/G]ATTCCCTCCCTCTGA | 5663 |
rs376331004 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137716 | TCAGGAAGGAAAAGG[C/T]TGGCAGGGATTTTGA | 5663 |
rs376338548 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73191552 | CATATATTTTTTTTT[-/T]CTTTTCTTTTTTAGT | 5663 |
rs376393791 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73162941 | TTTCTTTGAGACCAT[A/G]TGAATGTTTTACCTA | 5663 |
rs376400981 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186707 | GCTTGAACCCAGGAG[A/G]CAGAGGTTGTGGTGA | 5663 |
rs376433615 | snp | C/T | 4.9423e-05 | 0.00497082 | missense | PSEN1 | GRCh38.p7 | 14:73211876 | CCTCATCGCTCTACA[C/T]CTGAGTCACGAGCTG | 5663 |
rs376484059 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73162199 | AAAAAAAAAAGTTAA[A/G]TAGAAAAAGGACATA | 5663 |
rs376510924 | in-del | -/TCTA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73158283 | TATTTAACTTTTTTT[-/TCTA]TCTATCTATCTATCT | 5663 |
rs376532187 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73150534 | TTTGGGAGGCCGAGG[A/C]TGGTGGATCACAAGG | 5663 |
rs376549150 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73195716 | CCTGTCTCAGCCTCC[C/T]GAGTAGATAAGACTA | 5663 |
rs376560207 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151097 | AAAAAACTTTATGTG[A/G]TTTATGTCTGAAAGT | 5663 |
rs376746568 | in-del | -/CTTT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73188773 | GGTTTTCTTTTCTTT[-/CTTT]TGTTTGTTTGTTTTT | 5663 |
rs376753943 | in-del | -/TGCTGTCAGCCC | 0.00119737 | 0.0244387 | utr-variant-3-prime, cds-indel | PSEN1 | GRCh38.p7 | 14:73220307 | TGTGTTATGAATCGG[-/TGCTGTCAGCCC]TGCTGTCAGACCTTC | 5663 |
rs376820395 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73200925 | GTGTGGTGGTGCACA[C/T]TTGTAATCCCAGTTA | 5663 |
rs376825259 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209450 | GATTGTCTGTGAGCA[G/T]GTAGGTATATATGTA | 5663 |
rs376883976 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73201290 | ACGGGGTTTCACCAT[C/G]TTAGCCAGGATGGTC | 5663 |
rs376893399 | snp | C/T | 1.65534e-05 | 0.00287688 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173753 | ACCCTGTTCTTCTTA[C/T]GGTTGGGTATTCTTG | 5663 |
rs376897161 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | PSEN1 | GRCh38.p7 | 14:73182372 | GTGGTGTACCCACGC[A/C]TATAGTCCTAGGTAC | 5663 |
rs376920764 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73155355 | GCAATTAACTTAGAG[A/T]TTTATTTAAATTAAA | 5663 |
rs376923743 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73181697 | ACAGTACACTAGTTG[A/G]TTCTCACTGTTAAGG | 5663 |
rs376967558 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73183641 | ATCAACAGGATCCCA[A/C]GGCAGAAGAAGTTTT | 5663 |
rs376992376 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156257 | GGTACTTGGGAGGCT[A/G]AGGTCGGAGGATGAC | 5663 |
rs377040096 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206477 | TAATGCAGAAAGTAG[A/G]TAACTTTTATTAGAT | 5663 |
rs377053325 | snp | A/G | 8.30792e-05 | 0.00644459 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73206426 | GGCAGAAGGAGACCC[A/G]GAAGCTCAAAGGAGA | 5663 |
rs377086298 | in-del | -/CCCC | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220213 | AGCAGTCTTTTTCTA[-/CCCC]CAGCCAGTAAGGCAG | 5663 |
rs377090228 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156833 | ATGCCCAGCTAATTT[G/T]TTGTAATTTTAGTAG | 5663 |
rs377137048 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73189550 | CTGGGAGATGGAGGT[A/T]GCTGTGAGCCGAGAT | 5663 |
rs377151507 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223118 | ACCAACAAAGCTGTC[A/G]TCGGGCTCACAGCTC | 5663 |
rs377193019 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212256 | GCTGGGACTACAGGC[A/G]TGCGCCACCACGCCT | 5663 |
rs377358533 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73142558 | GCAGGAGTTTGAGGT[C/T]TTGTTGTTACATTGG | 5663 |
rs377365367 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73165908 | TAAAAATACAAACAT[-/T]AAGCCGGCGCAGTGG | 5663 |
rs377422461 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73193566 | AAAAAAAAAAAAAAG[C/G]AAAAAAAAAAAAGCA | 5663 |
rs377462613 | snp | A/G | | | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73224142 | GTCAGAAGAAACTGT[A/G]AACTTATAAGACGTA | 5663 |
rs377464253 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73184926 | TCCTCACCTCCCAGA[C/T]GGGGTCGCGGCCGGG | 5663 |
rs377475251 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73141734 | AAGTTGCAGTGAGCC[A/G]TGATCGTGGCATTGC | 5663 |
rs377504261 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208536 | CCACAAGCAGGTCAT[C/T]CCATCATCTCTGCAG | 5663 |
rs377527557 | snp | C/T | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135492 | CCTGCTGCAGCCTCC[C/T]GAGTAGCTGGGATTA | 5663 |
rs377532245 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73155918 | AACTGTGGACTGTCA[A/G]TGTAGGTTCATCTGT | 5663 |
rs377538528 | snp | C/T | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135234 | GCTAATGGAAAATAT[C/T]ACTTTTGTTCTTAAA | 5663 |
rs377706684 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73212895 | CAAGAGTGAAACTTG[A/C]TTAAAACATTACAAC | 5663 |
rs386778764 | multinucleotide-polymorphism | AGTTTC/CAAAAT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73161415 | TAGCAATATTTTGTA[AGTTTC/CAAAAT]ATTGTACAGGATATT | 5663 |
rs386778765 | multinucleotide-polymorphism | CT/TG | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73162097 | GGCAGGAGAATCACT[CT/TG]AACCTGGGAGGCCAA | 5663 |
rs397810471 | in-del | -/CTAT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73158335 | TATCTATCTATCTAT[-/CTAT]TTTTAAGACGGAGTT | 5663 |
rs397824012 | in-del | -/T | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73202221 | GCTAATTTTTTTTTT[-/T]CCATATTTTTAGTTG | 5663 |
rs398025626 | in-del | -/A | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73140228 | GGGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 5663 |
rs398025627 | in-del | -/A | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73159196 | AGACTCTGTCTCTTT[-/A]AAAAAAAAAAAAAAA | 5663 |
rs398025628 | in-del | -/A | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73183304 | AATAAAAAATAAATT[-/A]AAAAAAAAAAATACA | 5663 |
rs398025630 | in-del | -/A | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196499 | GTAAGACCGTGCCTC[-/A]AAAAAAAAAAAAAAA | 5663 |
rs398025631 | in-del | -/T | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204543 | TATTCTTCCTTGTTC[-/T]TTTTTTTTTTTTTTA | 5663 |
rs398025632 | in-del | -/T | 0 | 0 | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73223949 | CATTTGTTTCTAAAC[-/T]TTTTTTTTTTTGAGA | 5663 |
rs398057232 | in-del | -/ACTCA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73161487 | TGCTAGAAAGACTCA[-/ACTCA]GAGAATGTTTTATAC | 5663 |
rs527255223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212321 | TCACCATCTTGGGCA[A/G]GCTGGTCTTGAACTC | 5663 |
rs527281456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212798 | GCTCAGTCATCTCTT[C/T]AGTTAGTCTTAGAGA | 5663 |
rs527304815 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204387 | TGAAAAGTGATTTTT[A/T]AAAAAATATTATTTT | 5663 |
rs527356802 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160448 | TTGCTGGGTCATATG[G/T]TAGTTTAATTTTTTG | 5663 |
rs527363702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152665 | CTTTGAGAGCATTCT[C/T]ATGTTCTTATTGGTA | 5663 |
rs527377893 | in-del | -/AATTATA | 0.00398564 | 0.0444627 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154296 | TATTCAACTACACAC[-/AATTATA]AACTTAATTGCAGAG | 5663 |
rs527401508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73153607 | CCTGTCCTACAGAGC[A/G]GGCTTAGAGCCCCAC | 5663 |
rs527420098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206078 | AACTAGTCCAGCTAT[C/T]GTTTCAGTGGAATCT | 5663 |
rs527437767 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73146071 | AGATCGTGCCACTAC[A/G]TTGCAGCCTGGGTGA | 5663 |
rs527460659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73199685 | CCTCCTAAAAAAGCT[A/G]TGCCTGTTTACATTC | 5663 |
rs527495440 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200432 | ATGCCACCACGCCTG[G/T]CTGATTTTTGTATTT | 5663 |
rs527508398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193138 | AACATGGCAAAACCT[C/T]GTATCTACAGAAAAT | 5663 |
rs527534196 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73219044 | AATATTCAGTTAACT[A/G]TGTTAAAAACCAAGA | 5663 |
rs527574235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73146880 | CTGTGAAAAGGAAGA[A/G]TTGAAATCATAAAGA | 5663 |
rs527611632 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139289 | CTTCGTTTTTTTTTT[A/T]AAAAAAGGCTGGGCA | 5663 |
rs527641069 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210852 | AAATGAAGGAAGAAT[-/A]AAAAGTACTTTGAAC | 5663 |
rs527679831 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73218022 | TGAACTCCTGACCTC[A/G]AGTGATGTGCCTGCC | 5663 |
rs527717823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73182259 | CTGAGACCAGAGGAT[C/T]ACTTGAAGCCAGGAG | 5663 |
rs527752957 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169073 | GGAATTATCCAGTCT[C/T]ATCTCAATCCGACTT | 5663 |
rs527753334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73178481 | ACGTGAGCCACCATG[C/T]CTGGCTCTTTACCCT | 5663 |
rs527791186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169565 | TGTTCCTTATCTCTA[C/T]CAATGCTAGTTCCTT | 5663 |
rs527792108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73161569 | ACAGAAAAAGACACA[C/T]AGGGCAGGGTCCAGG | 5663 |
rs527811026 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221881 | ACACGGGACAGGCGG[A/T]GGTTATAGAGTCGGG | 5663 |
rs527814167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73213810 | CCACTTCATACTCAC[C/T]AGATTGGCTATAATA | 5663 |
rs527840440 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73156829 | ACCATGCCCAGCTAA[-/T]TTTTTTGTAATTTTA | 5663 |
rs527844386 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73161240 | TTAGCCTCCCAAACT[G/T]CTGGGGTTGTAGATG | 5663 |
rs527884534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73207939 | AGGCATTACCTAAGC[A/G]GCTTTGACTACAGGC | 5663 |
rs528019788 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201139 | TGTCGCCCAGGCTGG[A/G]GTTCAGTGGGGCGAT | 5663 |
rs528028120 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73153471 | TCCAGGGAATCACAA[A/G]GCTTGGTCAGATGCT | 5663 |
rs528100291 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181085 | TACAGATTCCATGCA[A/T]AAGGCAAAGGTTCAA | 5663 |
rs528174184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73172724 | CAACTGGTTTAAATA[A/G]TGCACATACTTTCTC | 5663 |
rs528191966 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73164768 | CAAATTTCACACACT[A/G]TGATTTCACCCATAA | 5663 |
rs528192709 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208395 | TATCTGCAGGCAGGT[C/T]GTCCCATTGTCTCTG | 5663 |
rs528215754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217011 | CTAATTTTGTATATC[A/G]TTTACTGACTTCTCT | 5663 |
rs528374682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158033 | GCTTCTTTCTTTCAG[C/T]ATAATTATTTTGAAA | 5663 |
rs528408119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204453 | AACATGGGGTTAGCA[A/G]ACTACTGCTTGAAGC | 5663 |
rs528464186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197184 | GTGATCCGCCCACCT[C/T]GGCCTCCCAAAGTGC | 5663 |
rs528490070 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197661 | TAGAAGTGACTTCTC[C/T]CTGTTTCTGCTCACT | 5663 |
rs528527616 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73191282 | TCTCACACTACTTTG[C/T]ATAAATGGGATCATA | 5663 |
rs528605874 | in-del | -/TTTTTTTG | 0.00438332 | 0.0466095 | intron-variant | PSEN1 | GRCh38.p7 | 14:73175116 | CTTGAGGTCAGGAGT[-/TTTTTTTG]TTTTTTTGTTTTTTT | 5663 |
rs528614543 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73150138 | TGTAATAGGCACCCA[G/T]GTACCTATCACCCAG | 5663 |
rs528631438 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73146002 | ATCCCAGTTATTCGG[A/G]GGGCTGAGACACGAA | 5663 |
rs528650126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137792 | GCTAGCCAATAGAAA[C/T]AAAATGTGAGGCCCG | 5663 |
rs528685006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192185 | GCTCATGCTTGTAAT[C/T]CCAGCACTTTGGGAG | 5663 |
rs528782446 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | PSEN1 | GRCh38.p7 | 14:73167882 | TTACCTTCTCAGTTC[A/T]CAGTTATTTTCCAGC | 5663 |
rs528833403 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73147078 | GCAACCTCCACCTCC[C/T]GGGTTCAAGCTTTTC | 5663 |
rs528845963 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73207830 | GGAGTGCATGAGCAA[G/T]TGAGTGCAGGGTCCA | 5663 |
rs528847035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154735 | AAAGGAACATGAACA[A/G]CTTAACTCAGTAGCA | 5663 |
rs528869171 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200660 | CATCTCTAATCTTAA[G/T]GCCTTATCAAGTACT | 5663 |
rs529009573 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73140474 | TCAGCCTCCCAAAGT[A/G]CTGGGATTACAGGTG | 5663 |
rs529043789 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141135 | TCATGCCCAAAGACT[G/T]AGGAGTGGGTAGTAG | 5663 |
rs529075455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194958 | TTTGATTGACGAAGA[A/G]GTCTGTGGAAATAGG | 5663 |
rs529089245 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187014 | TTTGTTGATGAATTA[A/C]TCTGAAGTTTTAATT | 5663 |
rs529182430 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73199937 | TTTTTAGTGGAGACA[C/T]GGTTTCACCATGTTG | 5663 |
rs529270650 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73215854 | GTTGCTGGTGGAAAT[G/T]CAGACTGGTACAGCC | 5663 |
rs529348747 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73216401 | GCTCTATTAATTTTC[C/T]ACAATCATTGAATCA | 5663 |
rs529349172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73163630 | TTAAAACCAGATCAA[C/T]GTAGAGAAAGGCTTC | 5663 |
rs529361965 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194833 | TCGGCCTCCCAAAGT[G/T]TTGGGATTACAGGCA | 5663 |
rs529398491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73149346 | TTTTAATTTTCCCAC[A/G]GTTATGGTACATCTG | 5663 |
rs529409183 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73218060 | CCCAAAGTGCTGGGA[C/T]TACAGGCGTGAGCCA | 5663 |
rs529495032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73188677 | CTAACATTATAAAAT[A/G]TATGCATCTCATTCT | 5663 |
rs529530986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73150130 | GCACATAATGTAATA[A/G]GCACCCATGTACCTA | 5663 |
rs529619657 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134917 | GATTGTTTCTAAGAA[C/T]AGTTCATCAGCATTT | 5663 |
rs529684611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73218751 | CATAGAGAAGCCCCC[A/G]CACAGCATAGAGAAT | 5663 |
rs529776058 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73167802 | TTTTTCAAGTTAAAT[C/T]ACTCTCTATTGCAAG | 5663 |
rs529787423 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73160773 | AAAAAATCTGATGAT[A/T]TGTTTTTTTCCAATT | 5663 |
rs529791989 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152549 | GACTCAGAGGTTGCA[A/G]TGAGCTGAGATTGTG | 5663 |
rs529794579 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73158259 | ATATGATCCAATATG[A/G]TAGGTGTATATTTAA | 5663 |
rs529870326 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198672 | AGCAATCAAGGGAAA[G/T]AGTTGATCAGAGGAT | 5663 |
rs529920130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205904 | GTTTATTGCTTTTAA[C/T]GTTTTTTCTCACGCC | 5663 |
rs530034503 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193071 | ATCTTAGCACTTTGG[G/T]AGGCTGAGGCGGGCA | 5663 |
rs530065336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73185321 | CCTGGGCACCATTGA[A/G]CACTGAGTGAACGAG | 5663 |
rs530112898 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73180703 | GATACTGTTGTGTAC[C/T]ATAAAACAGCAGGGC | 5663 |
rs530216042 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73177021 | ACCTAATTTTTTCTG[G/T]ACCTTATTGCCATTT | 5663 |
rs530235019 | in-del | -/AA | 0.499 | 0.0223418 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143989 | GAGACCTTGTCTCTT[-/AA]AAAAAAAAAAAAAAA | 5663 |
rs530241839 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73213588 | TTGTGGGTACTTACC[A/G]AAAGGTTCAGTTGAC | 5663 |
rs530381844 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73205807 | GATGCACATGTGTAT[A/G]TCTAGATCTAGATTG | 5663 |
rs530430417 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148752 | AGCTTGGCCAACATG[A/G]AGAAACCCCATCTCT | 5663 |
rs530431091 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154348 | CATGTCTGTATTCCT[A/G]GTACTTTGGGAGGCT | 5663 |
rs530433528 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73161946 | GATCACCTGAGGTCA[A/G]GAGTTTGAGACCAGC | 5663 |
rs530439259 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73210549 | TACCAAAAGGGATGG[C/T]TAAAAGAGTTTAAGG | 5663 |
rs530593705 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73155136 | TTTATAACAGTGAGA[A/G]TGTGGCAGTAATCTC | 5663 |
rs530596157 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73180236 | GTGATCCACTGGTTT[C/T]GGCCTCCCAAAGTGC | 5663 |
rs530620059 | snp | A/C/T | 0.00676609 | 0.0577691 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134692 | ACCACGCCTGGCTAA[A/C/T]TTTTTTTGTATTTTT | 5663 |
rs530626195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216907 | GATAAATAACAGCAG[C/T]ATCTACAGTTAAGAC | 5663 |
rs530634518 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171502 | AGGCAAGTTACTTCT[A/G]TATAGAAGGGTGCAC | 5663 |
rs530797909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73164686 | TTGGGCTAATTACCA[C/T]TATATAATACAGTGT | 5663 |
rs530833971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73165336 | CTACATTCCCTGGCT[C/T]AAACGATTCTGGCTC | 5663 |
rs530854984 | in-del | -/TTTG | 0.0954501 | 0.196505 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201079 | GAGAATATCTTTTTG[-/TTTG]TTTGTTTGTTTGTTT | 5663 |
rs530879045 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210138 | TAAGGAAAAAACAAA[C/G]AAAAGAACTGAGAGA | 5663 |
rs530905734 | in-del | -/AAAAT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73146106 | GCAAGACTGTGTCTC[-/AAAAT]AAAGACAGGAACAAA | 5663 |
rs530918030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73203653 | TGACAGGAAATGTAT[A/G]AGCATTTTTGTTTTT | 5663 |
rs530940565 | in-del | -/TTG | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73143026 | TAACTGTTGTTGTTT[-/TTG]TTGTTCACAGGGCTA | 5663 |
rs530970418 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136378 | CGGAGGCCCCGCCCC[C/G]TTCCTCCTGGCTCCT | 5663 |
rs530981722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73150460 | GCATTATGTAATACA[C/T]TTGGCATGTTTTAAA | 5663 |
rs531093092 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73144338 | AGCCACTGCGCCCAG[A/C]CAGCTTATCCTTTTT | 5663 |
rs531119127 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73190546 | AGTAGAAAAGTATAT[A/G]TATGACATGTATAGA | 5663 |
rs531128279 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197534 | TAAAAAGGAGAAGGG[A/C]TGAATTTCTTCTACT | 5663 |
rs531161523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73191250 | GAATTAATATATCAA[C/T]TTCTCATCTACTCTT | 5663 |
rs531192385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206160 | TGAAGAGTTTTGTGA[C/T]AGCAGGTGCAGTTTG | 5663 |
rs531258859 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73153679 | TTTTTTTTTTTTTGC[C/G]CATTAAGTCTTAAAG | 5663 |
rs531341012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206996 | GATCAAATATTCTAG[A/G]TGGATATGACTTTTT | 5663 |
rs531417490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154287 | CTAAATTCATATTCA[A/G]CTACACACAATTATA | 5663 |
rs531426036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186282 | TACTTGGGGGGCTGA[A/G]GCAGGAGAATTGCTT | 5663 |
rs531455353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73146960 | CTAGGAGGGTGAACT[C/T]TGAGAGACACAGTCA | 5663 |
rs531476444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200521 | TCAGACTCCCAAAGC[A/G]TTAGTATTACAGGTG | 5663 |
rs531496532 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73199800 | ATGCAGGCTGGAGTG[C/T]AGTGGTGCGATCTCG | 5663 |
rs531554610 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194288 | ACAGGATCTCTCTCT[C/G]TCATCCACGCTAGAG | 5663 |
rs531561881 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73216197 | GGCGAGGCATGTATT[A/G]TATGAGTCATATGAA | 5663 |
rs531592504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186713 | ACCCAGGAGGCAGAG[A/G]TTGTGGTGAGCTGAG | 5663 |
rs531608522 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PSEN1 | GRCh38.p7 | 14:73155497 | CATAGAATCAAATAT[A/G]TATTATCATTATTAT | 5663 |
rs531663806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73170091 | CTGTCATGGTGTTGG[C/T]GGGGAGTGTCTTTTA | 5663 |
rs531711335 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221948 | CTGCTTAATAAAAAG[A/T]TGGAAGACAGTAAGG | 5663 |
rs531725305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73178575 | CCAATTTTTTTCACT[A/G]TTGTTCTGGTTAGAT | 5663 |
rs531744215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73214862 | GGATGGACGATGGTA[A/G]TGGTAGCACAATGAT | 5663 |
rs531842642 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195215 | TCTCGCTTTGTTGCC[C/T]AGGCTGGAGTGCAGT | 5663 |
rs531844391 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73176577 | ATTTAATTTTTCTGT[A/G]TTTTCATATTTTCAC | 5663 |
rs531887849 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73215739 | ATGGCTAAAAAGCAC[A/G]TGAAAAGATGCTCAA | 5663 |
rs531897493 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156442 | CAAATGCAAAAGGCT[A/T]CAAGTTCCTATCTTT | 5663 |
rs531913061 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73138168 | GTGATTATCCCTATT[C/T]TAAATTTTCTAATAA | 5663 |
rs531935146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73149179 | GGCAATAAGGTCTGG[A/G]TCAATAAAAAGAACT | 5663 |
rs531943525 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73163865 | GTTTTGATTTTGTTA[C/T]GAGCATGACAAGAAG | 5663 |
rs531950592 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73139455 | GTGTGTTGGCGTGTA[C/G]CTGTTATCCCAGCTA | 5663 |
rs531951903 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201643 | AGTAAATGTCATGTA[A/C]TACATCAAAGATTCC | 5663 |
rs531952945 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73157951 | AGATTGTGCCACTGC[A/T]CTCCAGCCTGGGCAA | 5663 |
rs532015003 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73172792 | GTACGGTGGCTTCAC[A/G/T]TTCATCAAGGACTCA | 5663 |
rs532018326 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73143470 | TTCACCTTTTCTGAG[-/T]TTTTTTTTTACATGT | 5663 |
rs532019276 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73175150 | TTTTTCCCCGAGACG[A/G]AGTCTCGCTCTTGTC | 5663 |
rs532094184 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | PSEN1 | GRCh38.p7 | 14:73178355 | ACCATGCCCAGCTAA[-/T]TTTTGTATTTTTATT | 5663 |
rs532141814 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73187361 | GGATCTAGTCTGTCA[A/G]AGAGAATAGTGAAGC | 5663 |
rs532167328 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181970 | GTAGAGACGGGGTTT[G/T]GGCATGTTGGTCAGG | 5663 |
rs532179026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204911 | ATCCATAAACCTCAT[A/G]CTTGGTGGTTGCCCT | 5663 |
rs532225222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217928 | GAGTAGCTGGGATTA[C/T]AGGTGCCTGCCACCA | 5663 |
rs532242398 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210412 | AAGAGTTACATTTGC[A/G]TGCACTAAAGGATGA | 5663 |
rs532251056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158471 | GCTGGGATTACAGGC[A/G]CCTGCCACCACACCC | 5663 |
rs532273338 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PSEN1 | GRCh38.p7 | 14:73218661 | CAGCATAAAGAATGC[C/T]CCCGCACAGCATAGA | 5663 |
rs532339312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212204 | CAAGCTCCACCTCCC[A/G]GGTTCAAGTGATTCT | 5663 |
rs532353470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198490 | TGAGATTGTTGAGCA[C/G]AAGGGTAATGTGAGC | 5663 |
rs532414960 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219921 | AAATATGTAGATTGC[C/T]TTTGGCAATTCTTCT | 5663 |
rs532424970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193002 | AATCATTAATTAGCT[A/G]TAGTAACTTTTTCAT | 5663 |
rs532437215 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73153628 | AGAGCCCCACATTTG[C/T]CATTGTAGAAATTCA | 5663 |
rs532459056 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73183443 | GGCAGAGGACCCTGC[G/T]GCCTTCCGCAGTGTT | 5663 |
rs532504935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145115 | CCAGGCTGGTCTCGA[A/G]CTCCTGGCCTCAAAT | 5663 |
rs532545478 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73174649 | GTCCCTATAAAATAC[A/G]GTATAACTAAAATCA | 5663 |
rs532577464 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220173 | CCCCAGATGCCTCCT[C/T]TGTCCTCATTCTTCT | 5663 |
rs532698728 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73208718 | CCCAGAAAATGCACC[-/A]TAAGTTCTCACTGTG | 5663 |
rs532735673 | snp | G/T | 0.0803491 | 0.183626 | intron-variant | PSEN1 | GRCh38.p7 | 14:73185045 | TCACTTCCTAGATGT[G/T]ATGGCAGCCGGGCAG | 5663 |
rs532744811 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201564 | CATGTCTCTGTGTTT[C/T]GCCAGTGCTGGCAGT | 5663 |
rs532750138 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73175190 | GGAGTGTGACAGCGC[C/G]ATCTTGGCTCACTGC | 5663 |
rs532910305 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148561 | AACGTAATCTGTGCT[G/T]TCGGACAAAGAGATT | 5663 |
rs532912129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73140543 | TTAACAGCAAAATCT[A/G]GCCTAGTTATCGTCT | 5663 |
rs532957791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195038 | GAAGTCATATACTCT[C/T]TCTGACTTTCATAAT | 5663 |
rs532981113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73188363 | TCAGATTCCTTAATA[A/G]ATAGACGGGGTCGGG | 5663 |
rs533005474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187925 | GAGAATTCAGCAATA[A/G]ATGAAAAGAATAATA | 5663 |
rs533047073 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223367 | TCTGTGTAGCAGGGA[C/T]GATTTCCCAGAAAGC | 5663 |
rs533052159 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141415 | CTGGAGAAATGATTT[G/T]CTCCTAGTCTCTTAA | 5663 |
rs533198551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73170448 | TGGTCTGAAATCACA[A/G]AAAGCTGAATTTGAA | 5663 |
rs533246140 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73197140 | GGGTTTCACCGTGTT[A/G]GCCAGGATGGTCTTG | 5663 |
rs533252285 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157235 | GGTTCAAGCGATTCT[C/T]CTGCCTCAGCCTCCT | 5663 |
rs533269170 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73163698 | GAGGGAACTGAGTGA[C/G]AAGGAACAGTCAGGT | 5663 |
rs533272380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73150384 | CTGAATTGGGTATTT[A/G]CCATGTTTAATAAAA | 5663 |
rs533284425 | in-del | -/AAG | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211125 | CAGTTGCCTTAAACA[-/AAG]AAGAAATTTATTCTT | 5663 |
rs533287554 | snp | A/G | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216277 | CTTAAGGCCTAGGGT[A/G]GGAGTGGGGATTAAC | 5663 |
rs533368800 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73202674 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATTG | 5663 |
rs533409791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156650 | GTTTGAACTTTTTCC[A/G]TAATAAAAAGTTTTG | 5663 |
rs533439082 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73142680 | TTGCTCCTGTGATAA[C/T]TTCTGAAGTGCTGAT | 5663 |
rs533441105 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143185 | TCTAGCTTTGCCTGC[C/G]CCTTTCTTTGTACCA | 5663 |
rs533487738 | snp | C/G | 0.0322114 | 0.122752 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136373 | CAGGCCGGAGGCCCC[C/G]CCCCCTTCCTCCTGG | 5663 |
rs533506110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73203470 | GTAAGAAAACCACAA[C/T]GCAATGCCGATGAGT | 5663 |
rs533543407 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196728 | GATCTGCTGCCTCAG[C/G]CTCCCCAAAGTGCTG | 5663 |
rs533545267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204132 | GCCTCCCGAGTCGCC[A/G]GGATTATAGACATGC | 5663 |
rs533595318 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73189604 | GCAACAAGAGTGAAA[C/G]TCCATTTCAAAAAAA | 5663 |
rs533622849 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73144910 | TTTTATTTTATTTTT[C/T]GAGATGCAGTCTTGC | 5663 |
rs533632372 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181113 | CAATTGTGGGTTTAT[C/T]CGTATGAGTAGACTA | 5663 |
rs533690128 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73191817 | CCTCCCAAATTGCTG[C/G]GATTAGAGTGTGAGC | 5663 |
rs533740952 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139753 | AGAAGTAATACCTGA[G/T]TAATTAGAATTCCCA | 5663 |
rs533761451 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73184396 | GGGCGGGGGGCTGAC[C/T]CCCCCACCTCCCTCT | 5663 |
rs533810469 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73214699 | AAGTGAAATAAGCTA[C/G]TTACAAAAAGAAAAA | 5663 |
rs533848084 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73193224 | CTGAGGTGGGAGGAT[C/T]GATTGAGCCCAGGAG | 5663 |
rs533857724 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219726 | ACGTTGAAAATCAAC[C/G]CAATAATTCTGTATT | 5663 |
rs533944404 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73138234 | TTTATTTATTTATTT[A/T]TTGAGACGGAGTCTG | 5663 |
rs533966057 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192540 | GGTAAAATTATAAAG[G/T]TGGGATATTAATATC | 5663 |
rs534033409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195299 | TGCCTCAGCCTTCCG[A/G]GTAGCTGGGACTACA | 5663 |
rs534036598 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209098 | ATCGGAGCCTGCAGA[C/T]GCAAGGGGCTTCCTG | 5663 |
rs534094973 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73207554 | ATACTTTCAACCAGG[A/C]ATTCCTATTTGGAAC | 5663 |
rs534099483 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PSEN1 | GRCh38.p7 | 14:73161164 | ATTTTTTGTAGAGAC[A/G]GAGTTTCACCATGTT | 5663 |
rs534134716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193342 | TCAAGCTTTTTGAGG[C/T]TTTGACAAGCTGGCC | 5663 |
rs534147887 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73220618 | GGGGCCTCCAGCAGC[A/G]AAGGGGATACAGTGA | 5663 |
rs534173940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154420 | TTGGGTAACATAGCA[C/T]GATCTTGTCTCTACA | 5663 |
rs534192266 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73161077 | CCTCCCAGGCTCAAG[C/T]AGTCCTTCCACCTCA | 5663 |
rs534234017 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168762 | GACACTGGAAGAGAA[A/C]CTGGGTGCCAAGAGG | 5663 |
rs534272069 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160680 | TATTACACAGATGTA[C/G]AGCATCTTTTCATGT | 5663 |
rs534278679 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223622 | TTTCAAATTCTTGGT[A/G]AGATATAATTTTGAT | 5663 |
rs534289847 | in-del | -/AAC | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73180836 | AATGCATATGAAAAT[-/AAC]AAATTAACATATTTG | 5663 |
rs534299312 | in-del | -/TTTC | 0.021333 | 0.101051 | intron-variant | PSEN1 | GRCh38.p7 | 14:73188766 | AGATGGAGGTTTTCT[-/TTTC]TTTCTTTTGTTTGTT | 5663 |
rs534307684 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PSEN1 | GRCh38.p7 | 14:73180445 | CCAGTATAACTAAAA[A/G]GATCTTTTGAGTCAG | 5663 |
rs534344531 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73202536 | GGAGTGCAGTAGCGT[A/G]ATCTCGACTCACTGC | 5663 |
rs534349859 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171551 | GGCAAGCGCACATTT[C/G]GACAAGGGAGGGGAA | 5663 |
rs534389257 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73176935 | GTGGGTTCTCTTTTC[A/G]TGCCTCCATGGAAAC | 5663 |
rs534401313 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73149172 | GTTACCAGGCAATAA[C/G]GTCTGGATCAATAAA | 5663 |
rs534430626 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73151166 | AAAGAGACATTCCTA[A/T]GTAGAATTTTGGGCA | 5663 |
rs534436924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73209654 | ACAGTTGTGATAGGT[A/G]CTACAAAGAAGACGT | 5663 |
rs534475356 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73156806 | TAGCTGCGACTACAG[A/G]CGTCCGCCACCATGC | 5663 |
rs534475682 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171414 | TCCCCCTCCTCTTGG[-/T]GTTATATATAAAGTT | 5663 |
rs534476110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73202944 | AAACAGTTCAACATA[C/T]GTGGGAAAATAGGAG | 5663 |
rs534479670 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73147156 | ACACCCGGCTAATTT[G/T]TGTATTTTTAGTAGA | 5663 |
rs534504185 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73192527 | GATATAGGTTATGGT[-/A]AAAATTATAAAGGTG | 5663 |
rs534510400 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73203785 | TAGAAGGGAAACTAA[A/C]AATTCCTTGAGGTAG | 5663 |
rs534513313 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73178430 | TGGCCTCAAGTGATC[C/T]GTCTGCCTCAGCCTC | 5663 |
rs534551192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193849 | TTTTGTAGAGAGAAC[A/G]TCTTGCTATATTGCC | 5663 |
rs534560557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216110 | ACCATTCAGCTTCCA[A/G]TAACTTCCAAGAAAC | 5663 |
rs534641411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73163247 | GTGCTTCATTTTCAG[C/T]GAACTACAAATCTCT | 5663 |
rs534665707 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136090 | TGGTGGGAGAGGGCA[A/G]AGATATTTGCGATTT | 5663 |
rs534712738 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156944 | TGGGATTACAGGCAT[C/G]AGCCACCACGCCTGG | 5663 |
rs534734279 | snp | C/T | | | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73223894 | AGTGAGCCGAGATCT[C/T]ACCACTGCACTCCAG | 5663 |
rs534818845 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73216502 | GTGGTGGCTCACGTC[G/T]GTAATCCCAGCACTT | 5663 |
rs534855792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73149840 | TGTTATAGTTCAAAT[A/G]GAAGATAACATCTAA | 5663 |
rs534856111 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157486 | TGTGGTATAATTGAC[A/G]TAAAATGTACATACT | 5663 |
rs534856914 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73218173 | CTCACTGCAACTTCT[C/G]CCTCCTAGGTTCAAG | 5663 |
rs534925418 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73174020 | AATATTGGAAGTATT[A/T]TATATGCATGGAATC | 5663 |
rs534944908 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73204790 | GCCTGTAATCCTAGC[A/C]CTTTGGGAGGCTGAG | 5663 |
rs534994389 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151490 | AATAAGAGAAGAAAA[A/G]CATGGGTGATCTTGG | 5663 |
rs535039283 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137326 | GAATAAAGTGTGAAG[C/T]TGACTAGGAGGTTTT | 5663 |
rs535041629 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73190759 | AAGAGGGGAACCATG[A/G]GGCACAGTGGGGAGA | 5663 |
rs535041966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181262 | CTGACCAACATGGAG[A/G]AATCCTGTCTCTACT | 5663 |
rs535079355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73172447 | GTATTATAGAACAAA[C/T]ATTGGCAAGCTACAG | 5663 |
rs535082253 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181779 | GGTTTTATTTTGTTT[C/T]GTATTTTTTTTTGAG | 5663 |
rs535128038 | snp | C/G/T | 0.00159649 | 0.0282165 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193788 | CAGCCTCTCAAGTAG[C/G/T]TAGAACTACAGGTGT | 5663 |
rs535154650 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73176879 | CACACATAGCTATTA[C/T]GTAAGATTCCTCTCA | 5663 |
rs535165738 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73217415 | CTACCCTGGCCACAC[A/G]TTAGAATCACTTGGG | 5663 |
rs535289882 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73166966 | AGTTCCTTTTGTATT[G/T]CTATAACAGAATACC | 5663 |
rs535320926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73218820 | TCACAGAGGCCAACA[C/T]ATCATTTAAGATAGA | 5663 |
rs535350728 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169806 | ATGTGCCACCATGCC[C/T]GACTAATTTTTATAT | 5663 |
rs535366599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154577 | CTGCACTTCAACCTG[A/G]GCAGCAAAGTGAGAC | 5663 |
rs535370013 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204630 | TGGACATTGATTTTC[A/T]TGTTACTATTAACTG | 5663 |
rs535378042 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222232 | GGAAGAAAACAGTCA[G/T]AAGTAAGCAATTTGT | 5663 |
rs535382685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139022 | GGCGCAGCGGCTCAC[A/G]CCTGTAAACCCAGCA | 5663 |
rs535386492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162397 | AATTGGTGCAATCCA[C/T]AGGGAGGGCAATTTG | 5663 |
rs535398796 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73141707 | GGAGAATTGCTTGAA[C/T]CCAGGAGGTGGAAGT | 5663 |
rs535429353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193296 | GCCTGGGTGATAGAA[C/T]AAGACCTTGTCTCAA | 5663 |
rs535435008 | snp | C/G | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136272 | GCAGCCTCAGAACCC[C/G]GACAACCCACGCCAG | 5663 |
rs535534919 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73191983 | CCAAAGTATAGTATG[A/G]CATTTTAGGTATGAT | 5663 |
rs535557692 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73199733 | GTATCAATTTCCTTA[A/C]CCCTTTGGTGTTTTG | 5663 |
rs535571420 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148687 | CCTGTAATCCCAGCA[C/G]TTTGGGAGGCTGAGG | 5663 |
rs535590491 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221450 | CTCTGAAGAGGGTAC[A/G]TGGGGTGTGTGTATT | 5663 |
rs535592152 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73161826 | ATTAGCGGAAACTTG[C/T]TGGCATGACCCAATG | 5663 |
rs535664961 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169309 | CTGGTTAAGCTTAGG[G/T]GTTATTTACACTTCT | 5663 |
rs535702249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179541 | AGTATTGCTTGAACC[C/T]GGGAGGCAGAGGTTG | 5663 |
rs535775729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73214989 | TTATTTTTTGAGACA[A/G]TTTCGCTCGTTGCCT | 5663 |
rs535775960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73207689 | TGTGGCTGGTGGCAC[C/T]TTTTCCTGAGATTTG | 5663 |
rs535814233 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73159334 | CTACAGATGTGTGCC[A/G]CTGCACCCAGCTAAT | 5663 |
rs535866588 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73168354 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAACA | 5663 |
rs535879353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204585 | AAACCTGAAATGTTT[A/G]CTCCCTGGCCATTTA | 5663 |
rs535883087 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158170 | GATAGTGGCTGTTAC[A/G]GATATTCATGTACAG | 5663 |
rs535941925 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151401 | ACTATTTTAGAGATT[G/T]CTAGGATTCTTCCAA | 5663 |
rs535981857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194643 | GCGTGATCTTGGCTC[A/G]CTGCAAGCTTCGCCT | 5663 |
rs536015171 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73191038 | TTTCTCCTCAGTTAC[C/G]TCAGGCATCTTCTAC | 5663 |
rs536064987 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73191699 | CTGCAGGCATGTGCC[A/G]TCAACTTTAGCTAAT | 5663 |
rs536083442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73214255 | CAACTATTGCTGGGC[A/G]CAGTGGCTCAAGCAC | 5663 |
rs536085327 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73189061 | CTCCCAAAATGCTGG[A/G]ATTACAGGCGTGAGC | 5663 |
rs536093631 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73182599 | CTATAATCCCAGCAC[C/T]GTGGGAGGCTAAGGA | 5663 |
rs536136523 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73138755 | CATGAGGTCAGGAGA[G/T]CGAGACATCCTGGCT | 5663 |
rs536165041 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223095 | TGTGAAATGGCTGGC[C/G]AGAGTGTACCAACAA | 5663 |
rs536170695 | snp | A/G | 0.00234255 | 0.0341436 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208818 | GAACTTCCCCTTTCC[A/G]CCTAGGAGCCTGTCT | 5663 |
rs536201818 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73173112 | GAAGATGGATATGTG[A/G]CATTATCTTAAGACA | 5663 |
rs536227799 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210973 | ATGAAATGACTGGCC[A/C]ATAAAGACATTCACT | 5663 |
rs536235404 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73183521 | AGCATGCTGCCTTCA[A/T]GCATCTGTTTAACAA | 5663 |
rs536241716 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PSEN1 | GRCh38.p7 | 14:73174525 | AGGCATGAGCCACTG[C/T]GCCCGGCCCTAAGTG | 5663 |
rs536276222 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73167356 | AAAGGAAATGCTTAT[G/T]GGAGTGTTTTAGATT | 5663 |
rs536396813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73144679 | GGGAATATCATAAAT[C/T]AGTTTGTTAAGCCTT | 5663 |
rs536402442 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136569 | CGGCGGCAGCGGGGC[C/G]GCGGGGAAGCGTATG | 5663 |
rs536418266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205636 | TTCCAAAATGTAATA[C/T]TGCTGGGTTAAAGGA | 5663 |
rs536419768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73213072 | GAACTTTCACTGGGC[A/G]TGTTCATGACTTTAC | 5663 |
rs536521777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145587 | CAAGTAGTAACACCC[A/G]TCTCAGCCTCCCACA | 5663 |
rs536539336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73137116 | TGTTTGCTGCTGCTT[C/T]CCTCTCAGATTCTTC | 5663 |
rs536642389 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187977 | GCTGTTGCCCAGGCT[A/G]GAGTGCAGTGGCATG | 5663 |
rs536677504 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73175468 | GCAACATAGTAAGAC[C/T]TATCTCTACCAAAAA | 5663 |
rs536678798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179406 | CAGATTGCCTGAGCT[C/T]ATGAGTTTATGACCA | 5663 |
rs536732471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171818 | ATTGAACATACTGGC[A/G]TATTAATTCTTTGAA | 5663 |
rs536733676 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73202762 | CAGGCGTGAGCCACC[A/G]TGCCCAGCCTATCAT | 5663 |
rs536786517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216035 | CAGAATAGCCCCAAA[C/T]TGAAAACAATCCAGA | 5663 |
rs536865221 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73209558 | GGATATAGCACTGAA[A/C]AAGATTTCCCCTGCC | 5663 |
rs536945572 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73150938 | CTGGGCGTGGTGACA[C/T]GCGCCTGTAGTCCCA | 5663 |
rs536961202 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73149665 | GGTTCTAGAACACAG[G/T]ACTTTCAGTTTTAAA | 5663 |
rs536966268 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73146286 | TCTAATTCCTGGACT[C/T]AAGCCATCCCCCCAC | 5663 |
rs536986616 | in-del | -/TGTTTT | 0.135784 | 0.222384 | intron-variant | PSEN1 | GRCh38.p7 | 14:73177397 | TTGTGTGTGTGTTTT[-/TGTTTT]TGTTTTTGTTTTTGT | 5663 |
rs536997863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73142210 | CAGCCCATTCATAAC[A/G]TTAGAAGTTGGGCCG | 5663 |
rs537001338 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200113 | TCTGAGAGAGAAAGA[C/G]ATCTAATAGGCAAAA | 5663 |
rs537073971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169989 | TGAGTTTTCTGGGAA[A/G]GAGGTGGGCAATTCC | 5663 |
rs537147204 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73141267 | TATTGGCTGAATAAT[A/G]ATCTAATCTACCACA | 5663 |
rs537176908 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73220831 | AACAGCCATCAGCCT[A/G]TGTGGGCTCAGGGCA | 5663 |
rs537193344 | in-del | -/TCT | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73213394 | TTTGTGTCCTCCTCC[-/TCT]TCGTCTCCAACTTTT | 5663 |
rs537212470 | in-del | -/TGTTTT | 0.00515682 | 0.0505155 | intron-variant | PSEN1 | GRCh38.p7 | 14:73177392 | GTTTTTTTGTGTGTG[-/TGTTTT]TGTTTTTGTTTTTGT | 5663 |
rs537239950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181166 | TAGTTTCAGCTGGGC[A/G]TGGTGGCTCACGCAT | 5663 |
rs537259989 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73202030 | GGGATTACAGACGTG[A/G/T]GCCACTGCACCCGAC | 5663 |
rs537277555 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73172412 | TATTATCCATATAGG[A/T]TAGGGTTAGGTTTGG | 5663 |
rs537282584 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156103 | ACTTTGGAAGGCTGA[A/G/T]GCGGGTGGATCACTT | 5663 |
rs537330564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148889 | AGTGAGCTGACGTCG[C/T]GCCATTGCACTCCAG | 5663 |
rs537372871 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194863 | ATGAGCCACCGTGCC[C/T]GGCCTGGCCATACAC | 5663 |
rs537458003 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73189117 | TTTCTTTATCACCAA[G/T]TATCTAGCATTGCTC | 5663 |
rs537462773 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73197748 | TTAAACTAGGAAGAC[A/T]TGTTCCTATACCCCA | 5663 |
rs537464120 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196798 | AATTTTTAAATGTAA[A/T]TGCATTTAAGTGACA | 5663 |
rs537496980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145350 | TTTATTATTTGTTTT[C/T]TTGAGACAGGGTCTC | 5663 |
rs537497099 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73189877 | CTTGACCTTTACCAT[A/G]TGTTGGTCTCCCTTG | 5663 |
rs537533737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73146133 | GGAACAAAGGTATCG[A/G]TAACTCTTAAGTATA | 5663 |
rs537572186 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73138860 | TAGTCCCAGCTACTC[G/T]GGAGGCTGAGGCAGG | 5663 |
rs537575886 | in-del | -/GGA | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179158 | CAGGGCCAAAATGTG[-/GGA]GGAGAGAGAGAAATA | 5663 |
rs537706540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73177389 | GGGGTTTTTTTGTGT[A/G]TGTGTTTTTGTTTTT | 5663 |
rs537774701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73218068 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCACCT | 5663 |
rs537844381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169160 | AGGGTCTTTTTAGCT[C/T]TCATCCTGCCAGACT | 5663 |
rs537949425 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PSEN1 | GRCh38.p7 | 14:73214993 | TTTTTGAGACAATTT[C/T]GCTCGTTGCCTAGGG | 5663 |
rs537964773 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73155007 | ACATGCCTTTTGGAA[A/G]TAATTTAGCAATTAA | 5663 |
rs537979644 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73188344 | ATAAGATTCCTGTTC[C/T]TGATCAGATTCCTTA | 5663 |
rs537997868 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208133 | CTGGCTTAGGGAACT[C/T]CTGAGTCTGGACTCC | 5663 |
rs538178628 | snp | A/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221306 | TATTATCATTGAGAA[A/T]GCACAGCTACAGCAA | 5663 |
rs538211657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73213899 | ACTGCTGGTGGGAAT[A/G]TAAAATAGTATAGTG | 5663 |
rs538237623 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73202118 | GGCGCAATCTCAGCT[C/T]ACTGCAACCTCCATC | 5663 |
rs538242853 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73164271 | AGTTCTAGGAGAGGT[C/G]AGAGATGGAGATCAA | 5663 |
rs538245906 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73207638 | GTTAGACTCTCACGG[G/T]ATCCTTAGGGTGTGA | 5663 |
rs538277889 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73164946 | CCAACACTTCTGTCA[A/C]AAAATTGTACTTTTT | 5663 |
rs538309317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154540 | TAGGAGGTCGAGGCT[A/G]CAGTGAGCTGTAATC | 5663 |
rs538343022 | in-del | -/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73153803 | CTGCAGCCTCTGCCT[-/C]CCAGGTTCAAGCGAT | 5663 |
rs538347986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73147224 | CTCCTGACCTCGTGA[C/T]CCGCCCGCCTTGGCC | 5663 |
rs538412782 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204494 | CCATGGCTTGTTTTT[G/T]TACAGCTTATAAGCT | 5663 |
rs538428827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196997 | GAGTGCAGTGGCGCA[A/G]TCTCGGCGCACTGCA | 5663 |
rs538453194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197229 | TGAGCCACTGCGCCC[A/G]GCCTATATGCTGAAT | 5663 |
rs538454686 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212405 | TGAGCCACTGTACCT[C/G]GCCTCCCTTCAGACT | 5663 |
rs538525201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73140704 | ACAAAATCCAAAAAA[A/G]TCTGAATTCTAAACA | 5663 |
rs538525600 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73161748 | GGCTGACCTCAGTTC[C/T]CTGGCCCCTTCAGAG | 5663 |
rs538569614 | snp | A/G | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135173 | TGAAGAATTTTAAAA[A/G]CATCTTTTTTCGTTC | 5663 |
rs538638546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181798 | TTTTTTTTTGAGACA[A/G]TGTCTCACTTTGTCA | 5663 |
rs538665754 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156970 | CCTGGCCTTTTTTTT[A/T]AAATGGTCTTACAGG | 5663 |
rs538733113 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158071 | ATGTTATGTGGTTCC[A/T]TTTTATTGCTGAGTT | 5663 |
rs538745966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73218342 | TCTGCCTGCCTCAGC[C/T]GCATAAAGTGCTGGG | 5663 |
rs538784834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73218999 | CCAGATTGAATGAAC[A/G]TCTGTTCTAAAATTT | 5663 |
rs538805943 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73151356 | AGTTTCTCAAAGATA[C/G]TTGCTGTGATTGGAT | 5663 |
rs538817677 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73179952 | TAATATATTTTTTGT[C/T]GCATTTGTACATCTT | 5663 |
rs538822200 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219615 | GACGCGTGGTCACAG[G/T]ACGATTTCACTGACA | 5663 |
rs538827744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212001 | GTAGCTACATTATCA[A/G]CCTTTTTGAGAATAA | 5663 |
rs538845486 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73190211 | AGAATTTTAAGGCTG[A/G]GTGTGGTGGCTCACA | 5663 |
rs538871034 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151353 | GTGAGTTTCTCAAAG[A/T]TAGTTGCTGTGATTG | 5663 |
rs538883913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143098 | GTCTTTTGCCACGCT[A/G]CCTGAACAGTGGGGT | 5663 |
rs538895089 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158911 | TTAGCTCTTATAAAA[A/T]GGTATATAGTTACAT | 5663 |
rs538936668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152112 | GAGGCGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 5663 |
rs538961286 | in-del | -/T | 0.260227 | 0.249791 | intron-variant | PSEN1 | GRCh38.p7 | 14:73147044 | AGGAGTCAGCCATTC[-/T]TTTTTTTTTTTTTTT | 5663 |
rs539042845 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73182378 | TACCCACGCCTATAG[C/T]CCTAGGTACTAGGGA | 5663 |
rs539055952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173427 | TTAAAAATTCTTAGC[C/T]AGATTGGTGAGTTGG | 5663 |
rs539160906 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222358 | CCTTTTGCAATAGAT[A/G]CCCAAACAGATGATG | 5663 |
rs539230182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212466 | TTGGCATTTATTTTA[C/T]AAAGTAAAAGATTTG | 5663 |
rs539231782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73167177 | TATGCCATGGTGGAT[A/G]GACAGAACGGCAAGA | 5663 |
rs539268753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168170 | AGACCAGCCTGGCCA[A/G]CATGGCAAAACCGTA | 5663 |
rs539289799 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73159900 | TGATCTTGGCTCATG[C/G]CAGCCTTCACCTCCT | 5663 |
rs539356191 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148201 | GGGGCTAGGCAGGCT[G/T]TCTCTACTTTACCAC | 5663 |
rs539359790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156033 | TTTTGCTGTGGATCT[A/G]AGTTTGCATTTAAAA | 5663 |
rs539387360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198230 | GTACTTGTTCTCATC[C/T]TAAATGCACAGCATT | 5663 |
rs539401985 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73140431 | GGCCAGGCTGGTCTC[C/G]AACTCCTGACCTCGT | 5663 |
rs539460923 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73177801 | CTTTCAAAATTTTCT[A/T]TTTCTTTTCAGCAGT | 5663 |
rs539491442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148847 | CTGAGCCAGGAGAAT[C/T]GCTGGAACCCAGGAG | 5663 |
rs539500632 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73178794 | ATTTTTATGCTCCAA[A/G]GATTTTGATATTTTT | 5663 |
rs539531000 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141679 | AATCCTAGCTACTCA[A/G]GAGGCTGAGGCAGGA | 5663 |
rs539557983 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73188911 | CTCCTGCATCAAGGC[C/T]TCCCAAGTAGCTGGG | 5663 |
rs539572755 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | PSEN1 | GRCh38.p7 | 14:73215268 | GCCCGGCCAAAAAAA[A/T]TTTTTTTAAATACCG | 5663 |
rs539576682 | in-del | -/AGA/GA | 0.00147059 | 0.0270764 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162473 | TCTCTCCATGAGAAG[-/AGA/GA]GAGAGAGAGAGAGAG | 5663 |
rs539627812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73189025 | CAAACTCTTGACCTC[A/G]GGTGATCCACCTGCC | 5663 |
rs539634168 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192346 | CTTAGGAGGCTGAGC[A/T]GGGAAGACCACCTGA | 5663 |
rs539668175 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73143930 | GGAGTTCAAGGCTGC[A/C]GTGAGCTATGATTGC | 5663 |
rs539688018 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73155290 | GATCTTTGGCAAATT[A/T]ACTGGCCTCGCTAAA | 5663 |
rs539692479 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220147 | TGTAGACATACTTGT[A/G]CGCTCACTTGCCCCA | 5663 |
rs539701676 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171736 | AGGTAACTGGAATGA[G/T]GGTGGAGCAGGTAAT | 5663 |
rs539760205 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73147547 | CCTTAAGATTACTCA[A/G]CTCCCTTTGCTGGAA | 5663 |
rs539774357 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201277 | ATTTTTAGTAGCAAC[A/G]GGGTTTCACCATGTT | 5663 |
rs539810377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201962 | ACATTGGCCAGGCTG[A/G]CCTTGAACTCCCCAC | 5663 |
rs539817972 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73190362 | GGCGTGGTGGTGCAT[G/T]CCTGTAGCCCCAGCT | 5663 |
rs539851961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181478 | CAATCATAGTTTCAC[A/G]CCAGGTGCAGTGGCA | 5663 |
rs539886832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73144102 | CAGGAATGCAGTGGC[A/G]TAATCTCAGCTGACT | 5663 |
rs539893163 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136344 | GCTCTGGGTTCTCCC[C/T]GCAATCGTTTCTCCA | 5663 |
rs539981128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195916 | GGTAAATTATTTGCC[C/T]AAGCCTAAACTCTGA | 5663 |
rs539983327 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73162179 | GCAAAACTCCATCTC[-/A]AAAAAAAAAAAAAAG | 5663 |
rs540019509 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73198457 | TGTCTTTCTGCTATT[C/T]GGTGACCACTGGGGA | 5663 |
rs540119262 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157674 | TGTTTTGTCACCGCG[C/T]GCAGCCATTTACTAT | 5663 |
rs540125111 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73202619 | CTGGGACTCTAGGCG[C/T]CCGCCACCATGCCTG | 5663 |
rs540159238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216499 | TGTGTGGTGGCTCAC[A/G]TCTGTAATCCCAGCA | 5663 |
rs540189613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205228 | ACGCCTGTAATCCCA[A/G]CACTTTGGGAGGCTG | 5663 |
rs540226718 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73191152 | CATTCATTGTTTTTT[A/T]AAAAAAGACATTATA | 5663 |
rs540297726 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208573 | GTGGAGAGGAGACCC[A/G]GAGTGGGTAGCTTCT | 5663 |
rs540305623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136620 | CAAGCCAGGAAGGCA[C/T]CGCGGACATGGGCGG | 5663 |
rs540402394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192263 | GGCAACATGTTGAAA[C/T]CCTATCTGTACAAAA | 5663 |
rs540423054 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151428 | CCAAAGTGTATATTG[C/T]AGGCCAGGCATGGTG | 5663 |
rs540481709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73167514 | AGGCAGAGTCCTCAT[A/G]ACCCAGTCACCTCCT | 5663 |
rs540505960 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73189522 | GAGGCTGAGGCAGGA[G/T]AGTGGCGTGAACCTG | 5663 |
rs540540587 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73169915 | CCTCCCAAAGTGCTG[C/G]GATTTCAGGCGCCTG | 5663 |
rs540579405 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208501 | CAGTGGAGAGGAGAC[C/G]CGGAATGGGTATCTC | 5663 |
rs540661641 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152438 | AACCCCATTTCTACT[A/T]AGAAAAAAAAAAAAA | 5663 |
rs540696305 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73178162 | TGGCCTTAAGTATTC[C/T]GCCTGCCTGGGCCTC | 5663 |
rs540700392 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145092 | TGGACAGGGCTTCAC[A/C]ATGTTGGCCAGGCTG | 5663 |
rs540700493 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73153057 | CCTGTCTCAAATAAA[A/T]ACATAGACAAAAAGC | 5663 |
rs540734444 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73152004 | GCAAGTTCTGCATCC[C/T]GGGTTCACGCCATTC | 5663 |
rs540736753 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145713 | CAGTTTGTATTGAAT[A/G]CATATTGTTTTTGCA | 5663 |
rs540754290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73202109 | GAGTGCAGTGGCGCA[A/G]TCTCAGCTCACTGCA | 5663 |
rs540788268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192962 | AGAGAAAATGGTAAC[A/G]TGTACATCCCATAAC | 5663 |
rs540828972 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PSEN1 | GRCh38.p7 | 14:73184764 | CCCCCCACCTCCCTC[C/T]CGGACGGGGTGGCTG | 5663 |
rs540867989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73138546 | TTTTAGAGATGGGAG[C/T]CTCACTATGTTGCCC | 5663 |
rs540911355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141795 | CATCTTGGCCGGGTG[C/T]CGTGGCTCACGCCTG | 5663 |
rs540971598 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73175946 | GTACCCCACCAGTGC[C/T]GAATTTCTTTTTTAA | 5663 |
rs541094037 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156215 | ATAGTAATTAACTGG[G/T]TGTGGTGGCATGTGC | 5663 |
rs541105674 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73224093 | ACATCCTGAAAGATA[C/T]TTTTTCTAATAACTT | 5663 |
rs541118026 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73218189 | CCTCCTAGGTTCAAG[C/T]GATCCTCCTGTCTCA | 5663 |
rs541127729 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141268 | ATTGGCTGAATAATA[A/C]TCTAATCTACCACAG | 5663 |
rs541149866 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194973 | AGTCTGTGGAAATAG[A/G]ATTGAACTGGTTCTG | 5663 |
rs541221438 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157201 | CATGATCTTGGCTCA[C/T]TGCAACGTCTGCCTC | 5663 |
rs541233946 | in-del | -/AAG | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200757 | TGGAAAAGCAGTTTC[-/AAG]AAGGAGAGAGGCTGG | 5663 |
rs541274268 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73175149 | TTTTTTCCCCGAGAC[A/G]AAGTCTCGCTCTTGT | 5663 |
rs541293066 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73169131 | ACCCTTGATGAACTT[C/T]CCATTGTCAATTCAG | 5663 |
rs541333271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143153 | TTGTTTTCAGCTGAT[A/G]CTGGACCGAAATCAA | 5663 |
rs541335089 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135302 | TGTTTTTGAACAAGG[G/T]TGGCAGTGGGTTGGG | 5663 |
rs541385514 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179953 | AATATATTTTTTGTC[A/G/T]CATTTGTACATCTTT | 5663 |
rs541419804 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73165837 | CCAAGGTGGGCGGAT[C/T]ATGAGGTCAGGAGTT | 5663 |
rs541446557 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73174995 | TTATCACAAGTCATG[C/G]ACCTTTTAAGGTCAT | 5663 |
rs541461417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171830 | GGCGTATTAATTCTT[C/T]GAAATTTAGAACTCA | 5663 |
rs541503488 | snp | C/G | | | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137665 | GAGAACCACCACAGC[C/G]CAGGGTCGCCAGAGC | 5663 |
rs541577396 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73220706 | TTTGTGGTCTCTGCC[C/T]GCGTTACCTTTCCTC | 5663 |
rs541594136 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73203427 | GTAAGAATTTTTTCT[C/T]ACATTTTTCTTACAT | 5663 |
rs541611365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73165242 | ATTACAGGCATGAGC[C/T]ACCACGCCCGGCCCA | 5663 |
rs541614893 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160364 | GTGGCTATGCACATA[G/T]CTGTTTGAGGTCTTG | 5663 |
rs541649420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168859 | CGCGTTGAAGGAGCA[C/T]TGATTGTAACACACT | 5663 |
rs541649786 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160951 | TGGATATTAATCTCT[G/T]ACCAGATATATGATT | 5663 |
rs541821580 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73184720 | ACCTCCCTCCCGGAT[G/T]GGGCGGCTGGCCTGG | 5663 |
rs541821858 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200856 | AGGAGTTTGAAACCA[C/G]CCTGGCCAACATGGT | 5663 |
rs541823068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73175877 | CAAAATCTCGTTTTC[A/G]AAAAGCTTATATCAA | 5663 |
rs541832456 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186205 | ACCAACATGGAGAAA[A/C]TGTGTCTCTACTAAA | 5663 |
rs541855799 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145278 | TACTTGCTTTGCTTC[G/T]GAGGGATTATATGAG | 5663 |
rs541861671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168539 | CAGGTGAGCGTTGGA[A/G]ACTATGGATGGGACG | 5663 |
rs541884802 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73165340 | ATTCCCTGGCTCAAA[C/T]GATTCTGGCTCAAAC | 5663 |
rs541890226 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219952 | TCTCAAGCACTGACA[C/G]TCATTACCGTCTGTG | 5663 |
rs541936634 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139846 | TTAATACTCTTGCTT[A/G]GATGAGAGTGAGGAA | 5663 |
rs541967718 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186648 | CTAGCGTGGTGGCGC[A/G]CACGCGTGGTTCCAC | 5663 |
rs541997106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205962 | GAACATTCTAAAAAT[A/G]AGACATAATATGAAG | 5663 |
rs541997274 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73213382 | CTGAGAGGGCTCTTT[G/T]TGTCCTCCTCCTCTT | 5663 |
rs542041380 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179006 | TACTCACTCACCTTG[A/G]GAATGGACCCACAAG | 5663 |
rs542044921 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73213184 | TGCTCTTACAGCAGG[A/C]TTTAGCTTGCCTTTG | 5663 |
rs542084378 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73139143 | AAAAAATTAGCCAGA[C/T]ATGGTGCCAGGCACT | 5663 |
rs542134050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206732 | AAAGGTTCAGGCTGA[A/G]GTTATGATTTTGTTT | 5663 |
rs542134889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73215485 | CTATTCGAGAGGCTG[C/T]GGCAGGATAATTGCT | 5663 |
rs542291905 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73215752 | ACATGAAAAGATGCT[C/G]AACATCATTAATCAG | 5663 |
rs542352787 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73190275 | GGAGGATCCTTTGAG[C/T]CCAGGGGTTCTAGAC | 5663 |
rs542413495 | in-del | -/AAAT | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73166078 | ATAATAATAAAATAA[-/AAAT]AAAAGTAGTATCCAG | 5663 |
rs542428553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181858 | GGCTCACTGCACCCT[A/G]TACCTCCTGGGTTCA | 5663 |
rs542431035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169539 | CCTGTTTATCTTATT[A/G]TGTTCCATTGTGTTC | 5663 |
rs542469850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162016 | AAAAAAAAAAAAAAA[A/G]TAGAAAAAGAAACCA | 5663 |
rs542481543 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209678 | AAGACGTATAAGTTG[C/T]TATGAAAGTTTATAA | 5663 |
rs542493893 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217797 | TTTCAAAACTATGAT[A/T]TTTTTTTTTTTTTTT | 5663 |
rs542582661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204070 | ATGGCACGATCTCGG[C/T]TCACCACAGCCTCCG | 5663 |
rs542609279 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73216758 | GCAAAACTCCATCTC[-/A]AAAAAAAAAAAAAAT | 5663 |
rs542619466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197033 | CGCTTCCCGGGTTCA[C/T]GCCGTTCTCCTGCCT | 5663 |
rs542684946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143118 | AACAGTGGGGTCATT[A/G]ACCGCCATGCAATCC | 5663 |
rs542702916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212081 | TTTGGATATATCAGT[A/G]ATAGTGCTTTTTTTT | 5663 |
rs542722769 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135516 | GGGATTACAGGAGCG[C/T]GCCACCACACCCGGC | 5663 |
rs542759036 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73144492 | ACTAGTAATCAAAAT[A/C]GCTTCAAAATACCGT | 5663 |
rs542907969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73155386 | TGAGATAAACTGAAT[A/G]ATTAGTACACTACCT | 5663 |
rs542930566 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73151588 | GAAAAAGTAATCTCA[C/T]GCTGTCACCAAAGCT | 5663 |
rs542965719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73138452 | TCTCGATCTCCTGAC[C/T]TCGTGATCCGCCCGC | 5663 |
rs543011582 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73138804 | TCTACTAAAAAATAC[-/A]AAAAAAAAAAAAATT | 5663 |
rs543086429 | in-del | -/CTTT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73177698 | AAAAATGCTCTTCTG[-/CTTT]CTTTCAGCCTCCATG | 5663 |
rs543112247 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73174927 | AAGTGACCTACTGCT[A/G]AGTTTCAGCCAACTA | 5663 |
rs543113110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151662 | CTTGAGACCAGGGTG[A/G]TCTCAAGTGATCCTG | 5663 |
rs543148169 | in-del | -/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73203003 | GTAGGTTCAAGATTG[-/C]CATCTGTTCTTTTGT | 5663 |
rs543243254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192075 | TTTATATGAATGATA[C/T]AGAGCTTCCTATTAA | 5663 |
rs543248009 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145033 | TAGTAGCTGGGATTA[C/T]AGGCACGAGCTACCA | 5663 |
rs543285205 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137622 | GGAAGAAGAGCAAGG[A/T]GCCAGCTGAGGAGAA | 5663 |
rs543325928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141714 | TGCTTGAACCCAGGA[A/G]GTGGAAGTTGCAGTG | 5663 |
rs543391977 | snp | G/T | 1.6473e-05 | 0.00286988 | missense | PSEN1 | GRCh38.p7 | 14:73192717 | TGGAATTTTGGTGTG[G/T]TGGGAATGATTTCCA | 5663 |
rs543425886 | in-del | -/AGG | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197524 | ATACTGCTTTTAAAA[-/AGG]AGAAGGGATGAATTT | 5663 |
rs543440369 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73218039 | GTGATGTGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 5663 |
rs543469755 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154698 | GATATATCCCAATAT[A/C]CATAGAATTCTTATG | 5663 |
rs543471703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73161881 | GTTTATAGGCCGGGC[A/G]CAGTGGCTCACGCCT | 5663 |
rs543504374 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73147652 | TCTACCTTGAGCTTA[C/T]AGTAAATTTGTCAGT | 5663 |
rs543540913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201011 | AGCCATGATCGTGCC[A/G]CTGCACTCCAGCCTG | 5663 |
rs543568436 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73179195 | AAGGGCTATTTGCCC[C/T]ACTCTCTCGGGACTG | 5663 |
rs543599749 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73141805 | GGGTGCCGTGGCTCA[C/T]GCCTGTAATCCCAGC | 5663 |
rs543633439 | snp | A/G | | | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73224101 | AAAGATATTTTTTCT[A/G]ATAACTTTCACATTA | 5663 |
rs543640004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73164334 | TGCCGACGATTTTCT[A/G]TTGATAGACTAAAAA | 5663 |
rs543670801 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157178 | TTGCCCAGGCTGGAG[A/T]GCAGTGGCATGATCT | 5663 |
rs543710533 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73198666 | GGCAGTAGCAATCAA[A/G]GGAAAGAGTTGATCA | 5663 |
rs543759822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73149987 | TGCATAATCTCATTC[A/G]TAGTAAAGGGATTTG | 5663 |
rs543787152 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195329 | AAGTGCGCACCACCA[C/T]GCCCAGCTAATTTTT | 5663 |
rs543797875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73203244 | CCACCACGCCCAGCT[A/G]ATTTTTTGTATTTTT | 5663 |
rs543841936 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73182043 | CCTCCCAAACTGCTG[C/G]GATAACAGGCGTGAG | 5663 |
rs543854037 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137533 | GTTGATGTTGGAGCA[G/T]TGGAGAAGTCTAAGC | 5663 |
rs543882851 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173965 | AAGCAGCTTGGGCAA[A/C]GTAGCAAGACCCTGC | 5663 |
rs543920424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160645 | TAGTGATGTTGAGCA[C/T]CTTTTCTTTTTTCCC | 5663 |
rs543948769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216206 | TGTATTGTATGAGTC[A/G]TATGAAATGTCTAGA | 5663 |
rs543993486 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216556 | ATGAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC | 5663 |
rs544030867 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168512 | CAAGTGGCTGAGCAG[C/T]GAGCAGAGAATCAGG | 5663 |
rs544031190 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73159594 | AAAAAAGACTATTTT[A/C]TCCACTGAAGTGCCT | 5663 |
rs544038608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212226 | AGTGATTCTCCTGCC[C/T]CAGCCTCCCAAGTAG | 5663 |
rs544174377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73199488 | ATAGTGTTCTCTTAC[A/G]TAGATATTCAGTGGT | 5663 |
rs544210287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73191970 | AAACTAATATTTCCC[A/G]AAGTATAGTATGGCA | 5663 |
rs544213758 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73183042 | TCTTGGCCAAGACAG[A/T]CAAGTTTTAAAGAGT | 5663 |
rs544251391 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73174745 | ACTGGTCACACCTTG[C/T]CTAAACTGGTAGCCA | 5663 |
rs544254690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206658 | ACTCAAAACCCAACA[A/G]TACAGTCAAAGCATC | 5663 |
rs544352893 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73146638 | TAGTTAAGGGTTATT[C/T]TGAACTTGATACCTT | 5663 |
rs544365839 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73154718 | GAATTCTTATGAAAT[G/T]AAAAGGAACATGAAC | 5663 |
rs544379511 | snp | C/G | 0 | 0 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219810 | GCAGAATGGGGAATG[C/G]AGAGGTGGGCAGGGG | 5663 |
rs544420200 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73185095 | GGTGGGATGGCGGCC[A/G]GGCGGAGACGCTCCT | 5663 |
rs544487832 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221022 | TGATATGATATGACC[C/T]GGTTTGGGGCTGTCT | 5663 |
rs544494673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186552 | GAGTCTGAGGCGGGC[A/G]GATCACTTGAGGTCA | 5663 |
rs544494971 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212690 | AATGCAAGTATTTCT[G/T]CAGTGTCTAAGATGT | 5663 |
rs544612439 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195592 | CAATGTCTATCAGTA[A/C]ATTTTTTTCTGTTTT | 5663 |
rs544807309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73177003 | ATCTGCTGACCTTTT[C/T]GAACCTAATTTTTTC | 5663 |
rs544816722 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73162832 | TGTAGAAAGAAACTT[C/T]GAAAGGATTCACCAA | 5663 |
rs544893380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73180822 | ATAGTAATAAAAGAA[A/G]TGCATATGAAAATAA | 5663 |
rs544908520 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73208184 | ACTCCTCTCTTCTCT[C/T]CTTCTCGCCACCTGC | 5663 |
rs545059941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73149168 | GGAAGTTACCAGGCA[A/G]TAAGGTCTGGATCAA | 5663 |
rs545097747 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141841 | GGGAGGCAGAGGCTG[G/T]CAGATCACGAGGTCA | 5663 |
rs545098875 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134684 | CATGCGCCACCACGC[C/T]TGGCTAACTTTTTTT | 5663 |
rs545121002 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73203225 | CTGGGATTACAGACG[C/T]CTGCCACCACGCCCA | 5663 |
rs545131315 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157726 | TAGTATCATACAGGC[C/T]GGGCACGGTGGCTCA | 5663 |
rs545131607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73188376 | TAAATAGACGGGGTC[A/G]GGTGTGGTGGCTCAT | 5663 |
rs545232576 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143230 | TTCACCAGGCCTGAC[G/T]GAAGACCTAGCCCTG | 5663 |
rs545244095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181310 | AGCTGGGCGTGGTGG[C/T]GAGTGCCTGTAATCC | 5663 |
rs545260276 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205440 | GCCGAGATCATGCCA[C/T]TGTACTCCAGCCTGG | 5663 |
rs545270090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151002 | GAACCTGGGAGGCGG[A/G]GCTTGCAGTGAGCCG | 5663 |
rs545271126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73144202 | CACGTCACCATGCCT[A/G]GCTAATTTTTGTATT | 5663 |
rs545283399 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73145999 | GTAATCCCAGTTATT[C/T]GGGGGGCTGAGACAC | 5663 |
rs545308120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73144956 | GCGGTGCAGTGGCGC[A/G]ATCTTGCTTCACTGC | 5663 |
rs545439814 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73165306 | AGTATTTTTTTCCTT[A/T]AAGATGGTGTCTCAC | 5663 |
rs545488948 | snp | C/T | | | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73223930 | GCGACAGAGCAAGAC[C/T]CTGTCTCAAAAAAAA | 5663 |
rs545491272 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73201697 | TGACCTGACAGGAGA[A/T]CAGGTTTCAGGAAAG | 5663 |
rs545515859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211158 | TCACGTGACAGGAAG[A/G]CCTGAGGTGTAGGCA | 5663 |
rs545619962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151537 | TTTTCTAAATGTTCT[A/G]TAATACAGTTATTTA | 5663 |
rs545627699 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197411 | ATATTTGTGACCAAA[C/G]AGTAAAGAAGTAATA | 5663 |
rs545666290 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73147543 | CATTCCTTAAGATTA[C/T]TCAGCTCCCTTTGCT | 5663 |
rs545673812 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73161799 | CACAAGGCCCTCACC[A/G]TAGATCACATTATTA | 5663 |
rs545716734 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154647 | CCATGAACAAAGTCC[A/C]AAACAAACTAGGACA | 5663 |
rs545731488 | in-del | -/CA | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73183812 | CAATGAGCTGTTGGG[-/CA]CACACCTCCCAGACG | 5663 |
rs545794136 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73179533 | GAGGCAGGAGTATTG[C/T]TTGAACCCGGGAGGC | 5663 |
rs545833750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168893 | ATGCTGCTGCGGGGC[C/T]GCATAGAGCCTGCGC | 5663 |
rs545838429 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73140911 | GGGCTCTGCTTCCTT[G/T]TAGGTAGATGTGTGG | 5663 |
rs545840983 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73161012 | GGTTTTACTGTGTCA[A/C]CCAGGCTGGAGTAAA | 5663 |
rs545847431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194660 | TGCAAGCTTCGCCTC[C/T]CAGGTTCATGCCGTT | 5663 |
rs545884446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187438 | TACAGTTTGTAAACA[A/G]TTGCACTAGCTCTTA | 5663 |
rs545927835 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73141725 | AGGAGGTGGAAGTTG[C/T]AGTGAGCCATGATCG | 5663 |
rs545951029 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212714 | AAGATGTGTTGCCAC[C/T]TGATGGATTTAAGTT | 5663 |
rs545971793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73170056 | AGGTAACTTCCGGAC[A/G]TTGCCATGGCATCTG | 5663 |
rs545991340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73207722 | CAGGCCCACTGGGCT[C/T]ATTCCACCTACTCAG | 5663 |
rs546035164 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73175301 | CCGGCTAATTTTTGT[A/G]TTTTTAGTAGAGACT | 5663 |
rs546052493 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221614 | TTTTTAAAGGACAGG[A/G]TTTTGCTGTGTTGCC | 5663 |
rs546148878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186685 | AGGAGGCTTAAGCAC[A/G]AGAATTGCTTGAACC | 5663 |
rs546154623 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73215751 | CACATGAAAAGATGC[C/T]CAACATCATTAATCA | 5663 |
rs546160228 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181086 | ACAGATTCCATGCAT[A/T]AGGCAAAGGTTCAAT | 5663 |
rs546175191 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216184 | ATTAAGTAAAATAGG[C/T]GAGGCATGTATTGTA | 5663 |
rs546195102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73172239 | TCTCTACGACTCTCA[C/T]GGGGTCCAAAGAAGA | 5663 |
rs546211854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73209056 | GGTCATGACAGCACC[C/T]AGCCTCAGCCACAAC | 5663 |
rs546300429 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73182731 | GTAATCCCAGCTACT[C/T]GGGAGGCTAAGGCAG | 5663 |
rs546336401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73215559 | AAAAAAAAAGGAAAA[C/T]AAGCTACCAGCTGAG | 5663 |
rs546349237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210825 | TGCTCTGAACATGTA[C/T]TACTTTTATAAAAAA | 5663 |
rs546360831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217026 | ATTTACTGACTTCTC[C/T]CATTCATTGTGGGGT | 5663 |
rs546391770 | in-del | -/T | 0.171057 | 0.237209 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204298 | CCACCATGCCTGGCC[-/T]TTTTTTTTTTTTTTA | 5663 |
rs546422149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73164769 | AAATTTCACACACTA[C/T]GATTTCACCCATAAA | 5663 |
rs546471309 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208519 | GAATGGGTATCTCCT[A/G]TCCACAAGCAGGTCA | 5663 |
rs546487937 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73217820 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCTGTCACC | 5663 |
rs546609932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197207 | CAAAGTGCTGGGATT[A/G]CAGGCGTGAGCCACT | 5663 |
rs546698281 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217844 | TGTCACCCAGGCTGG[A/C]GTGGTGCAATCTCGG | 5663 |
rs546778993 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73147567 | CTTTGCTGGAAATCA[A/G]AAGTCATTAAGTATC | 5663 |
rs546797618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158052 | ATTATTTTGAAATTC[A/G]TCCATGTTATGTGGT | 5663 |
rs546849116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73183181 | GGAGTGCAATGGTGC[A/G]ATCTCAGCTCTCCAC | 5663 |
rs546876974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151236 | TTCTCTTGTGAATAT[A/G]TAAAAATAATTCTGT | 5663 |
rs546900251 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73182267 | AGAGGATCACTTGAA[-/G]CCAGGAGTTCAAAAC | 5663 |
rs547011941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151708 | AAGTAGCTGGGACCA[C/T]AGGCTCATGCCACCA | 5663 |
rs547014327 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143529 | TCTTTAAGACTCAAA[G/T]GGAAGAATAGATGTG | 5663 |
rs547031331 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201120 | TTGTGGCAGAGTCTT[G/T]CTGTGTCGCCCAGGC | 5663 |
rs547042060 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73136944 | TGCTTGAGCAACTGG[C/T]GAAACTCCGCGCCTC | 5663 |
rs547147441 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73140514 | GCACCTGGCCAAGGT[G/T]TTTTATAACTAATTT | 5663 |
rs547185521 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73174221 | AGCACAATCTAAGTG[A/G]GTTTTTGTTTGTTTG | 5663 |
rs547378176 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73215860 | GGTGGAAATTCAGAC[G/T]GGTACAGCCAGTGTG | 5663 |
rs547412673 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154831 | TGATCAGCCTTACTA[A/C]TAGGGATAAAAATTA | 5663 |
rs547443814 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148716 | GGCGGGCAGATCACC[A/T]GAGGTTAGGAGTTCA | 5663 |
rs547502849 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73138756 | ATGAGGTCAGGAGAT[C/G]GAGACATCCTGGCTA | 5663 |
rs547549246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187085 | TCAGTATTACTAATT[A/G]AGACATTCTTCTGTT | 5663 |
rs547579643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73149353 | TTTCCCACAGTTATG[A/G]TACATCTGGGCTGCC | 5663 |
rs547617537 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222242 | AGTCATAAGTAAGCA[A/C]TTTGTTGATTTTACT | 5663 |
rs547623041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179325 | GAGAATGGAGAAAAG[C/T]GGAAAAGAATGCCGG | 5663 |
rs547689473 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73189095 | TGTGCCTGGCTGAGA[A/T]GAAGGTTTTCTTTAT | 5663 |
rs547708731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73142052 | AGCCTGGGCGACAGA[A/G]GGAGACTCCGTCTCA | 5663 |
rs547723723 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73173099 | TGAGAAACAAGGGGA[A/G]GATGGATATGTGACA | 5663 |
rs547743578 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134923 | TTCTAAGAATAGTTC[A/C]TCAGCATTTTAAGAC | 5663 |
rs547767835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73188735 | GCTAGAAGCTTGCCT[A/G]TTAAGGTCAGGAATG | 5663 |
rs547838673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152029 | CCATTCTCCTGCCTC[A/G]GCCTCCCAAGTAGCT | 5663 |
rs547850078 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221388 | TCTAGAGTAATTTAT[C/T]TGTGTAAGGATCCCA | 5663 |
rs547891259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201850 | CTCCCAAGTTCAAGC[A/G]ATGGTCCTGTCTCAG | 5663 |
rs547900252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73167816 | TCACTCTCTATTGCA[A/G]GCCTCTTCCACCTTT | 5663 |
rs547974493 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73176187 | ATGTGTGATGATGAC[A/G]GGTTGTTACCAACAC | 5663 |
rs548020172 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73157129 | TTGAGAAAGATACCT[-/T]TTTTTTTTTTTGCGA | 5663 |
rs548037624 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73140169 | CAGAGTTCTGAAATC[C/T]GAAAACTAAAAGGTT | 5663 |
rs548061503 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196705 | GTCTCAAACTCCTGA[A/G]CACAAGTGATCTGCT | 5663 |
rs548077451 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135599 | GGTCTAGAACTCCCA[A/G]CCTCATGATCCGCCT | 5663 |
rs548113870 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73183635 | TCACAGATCAACAGG[A/C]TCCCAAGGCAGAAGA | 5663 |
rs548150697 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73185425 | CCTGGCCAACACAGC[C/G]AAACCCCGTCTCCAC | 5663 |
rs548176898 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73199573 | CAGCACTTACAGAGT[A/G]CATCCATGAACTTAT | 5663 |
rs548193365 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73138709 | CTCACCCCTGTAATC[C/T]CAGCACTTTGGGAGG | 5663 |
rs548215897 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193072 | TCTTAGCACTTTGGG[A/G/T]GGCTGAGGCGGGCAG | 5663 |
rs548244295 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179138 | GGACTTTATCTTCCT[A/C]AAGTCAGGGCCAAAA | 5663 |
rs548251656 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73211773 | TTCTCTTGAAGGCAC[A/G]GAAAGGGAGTCACAA | 5663 |
rs548288002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212298 | GTATTTTTAGTAGAG[A/G]TGGGGTTTCACCATC | 5663 |
rs548322586 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205395 | GAGGCAGGAGAATGG[C/T]GTGAACCCAGGAGAC | 5663 |
rs548383164 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223312 | TGGGTCCACCCTGAG[C/T]CCTGACATGTGGTGG | 5663 |
rs548394117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145222 | TTTTGCTTGCATTAC[C/T]CTTTCTTTGCCTTGT | 5663 |
rs548417229 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73213709 | GGATCTGAATGTTTA[G/T]TTCTCCCAAGAAAAT | 5663 |
rs548453832 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73207129 | CCGGATTACCCTGGG[A/C]AACTTATACCTTACC | 5663 |
rs548481843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168944 | GCTGGTTCCCGCATT[C/T]GTTTGCTCTGATTCC | 5663 |
rs548489616 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73207870 | CACAGCCAGGCATGC[G/T]GGCTGCAGCAGGGCA | 5663 |
rs548529166 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73158300 | TATCTATCTATCTAT[C/G]TATCTATCTATCTAT | 5663 |
rs548544310 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73188640 | TGACTCAGTCTCTAA[A/C]AATAAATAAATAACT | 5663 |
rs548558400 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73176837 | GGTCAGAATGGACAT[C/T]TGAGTCCAGAGTTTG | 5663 |
rs548565070 | in-del | -/TT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73146184 | TAGTTTTAAAAAATC[-/TT]TTTTTTTTTTTTTTT | 5663 |
rs548594211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179690 | CCTGATCCTCAAGCC[A/G]GAACTAGAGGTCTTC | 5663 |
rs548607017 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158389 | GGAGTGCAGTGGCAT[G/T]ATCTTGGCTCACTGC | 5663 |
rs548617542 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209024 | AGTGCTGCCCCAAGC[A/G]CCCGCACACCCGGCC | 5663 |
rs548627655 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73220463 | CAGAATTTGAACAAA[C/T]AGCCAAAAGCTGGTG | 5663 |
rs548712900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168704 | AATACAATCTTCTGC[A/G]TATACTACCCTTCAA | 5663 |
rs548767297 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223416 | CGTAATTGTTGAGAC[C/T]AGGCAGTTTCAAAGT | 5663 |
rs548786883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160657 | GCATCTTTTCTTTTT[C/T]CCCCCCATATTACAC | 5663 |
rs548789138 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73188163 | CGATCTCCTGACCTC[C/G]TGATCCGCCCGCCTT | 5663 |
rs548841684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210175 | GATGTGGTTGAGCTC[C/T]GTCAGAGCATTTCAG | 5663 |
rs548852417 | in-del | -/TTAA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73210882 | CTTCACTTATATATT[-/TTAA]TTATTTTTAATGTAT | 5663 |
rs548852446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73185798 | TCATGATCCGCCTGC[C/T]GTGGCCTCCCAAAGT | 5663 |
rs548858449 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154355 | GTATTCCTAGTACTT[G/T]GGGAGGCTGAGGCAG | 5663 |
rs548878380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210588 | AGTATCAGAAGTGAG[A/G]AGGGAGGGGGTAGAA | 5663 |
rs548879419 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200664 | TCTAATCTTAATGCC[A/T]TATCAAGTACTTACC | 5663 |
rs548975697 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73153176 | TAGCCTTTGACAGTG[G/T]TGTTGTATCATTATA | 5663 |
rs549022777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73203699 | ACAGAAAAAATATAC[A/G]CCTACTCTTTGAGCT | 5663 |
rs549039988 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134693 | CCACGCCTGGCTAAC[A/T]TTTTTTGTATTTTTA | 5663 |
rs549059248 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196802 | TTTAAATGTAAATGC[A/G]TTTAAGTGACAATAA | 5663 |
rs549099953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73150501 | GGGTGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 5663 |
rs549100609 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73180985 | GATATATTCTAAAGA[A/C]GGAATTAGAAATGCA | 5663 |
rs549137642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73172136 | CTCTCTAGACTCCTG[A/G]GGGGCTATCATGTGG | 5663 |
rs549173450 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73172586 | ACATTGTCTGTGGCT[A/G]CTTTCACACTACAGT | 5663 |
rs549176770 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73163974 | GTGGAGAATGGACTA[C/G]GGGAGCATAAAAGCA | 5663 |
rs549210403 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73146292 | TCCTGGACTCAAGCC[A/G]TCCCCCCACCTCAGC | 5663 |
rs549252467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157402 | CCTCGATCTCCCAAA[A/G]TGCTGGGATTACAGG | 5663 |
rs549320940 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173132 | ATCTTAAGACAACTC[C/T]AGTTGCAATTACTCT | 5663 |
rs549421462 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143095 | AGTGTCTTTTGCCAC[A/G/T]CTGCCTGAACAGTGG | 5663 |
rs549432238 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73138992 | AAAAAAATGTAAAAA[A/G]AGGCTGGGTGGCCGG | 5663 |
rs549467030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139442 | AAAAATTAGCCGGGT[A/G]TGTTGGCGTGTACCT | 5663 |
rs549535330 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73190605 | TAGTAGTGCTTTCCA[A/G]TCAGGCACGGTGGCT | 5663 |
rs549536983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154288 | TAAATTCATATTCAA[C/T]TACACACAATTATAA | 5663 |
rs549562229 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73191277 | TCTTCTCTCACACTA[C/T]TTTGCATAAATGGGA | 5663 |
rs549575619 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73147029 | TCTGAGGCTGGGAGT[A/C]AGGAGTCAGCCATTC | 5663 |
rs549584473 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73159338 | AGATGTGTGCCACTG[C/T]ACCCAGCTAATTCCG | 5663 |
rs549604209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73140140 | AAAGGTATATAGGAC[C/T]ATAGTCTCATATCCA | 5663 |
rs549608770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200635 | TAAAAATAAATTTCA[C/T]GGTAACTATCATCTC | 5663 |
rs549609306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73182223 | AAGCAAGACTGGGCA[C/T]GGTGACTCTCACCAG | 5663 |
rs549699559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73174065 | AAATTAGTGTAAAAT[A/G]TATATATTATGATTA | 5663 |
rs549701546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73199890 | GGCTGGGATTACAGG[C/T]GTGTGCCACCACACC | 5663 |
rs549742690 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73153751 | GGAGCCTCCCTCTGT[C/T]GCCCAGGCTGGAGTT | 5663 |
rs549792430 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194608 | GAGTCTGGCTCTGTC[A/G]CCCAGACTGGAGTGC | 5663 |
rs549815187 | in-del | -/T | 0.342806 | 0.232136 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194567 | TGCCTGGCCATACAC[-/T]TTTTTTTTTTTTTTT | 5663 |
rs549816415 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219607 | AGCAGCTTGACGCGT[A/G]GTCACAGGACGATTT | 5663 |
rs549817184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73155036 | AAATCTAACCTAATC[C/T]GATCTCACCTAGCAT | 5663 |
rs549819043 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73213820 | CTCACTAGATTGGCT[A/G]TAATAAAAAAGATAG | 5663 |
rs549884966 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169737 | TGCAGCCTCCACCAC[C/T]CAGGTTCAGGTGATT | 5663 |
rs549901137 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73191543 | AAATACGTACATATA[-/T]TTTTTTTTTCTTTTC | 5663 |
rs549933935 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73161779 | GCCAAGCTGATACTG[A/T]GTGACACAAGGCCCT | 5663 |
rs549939146 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193735 | AGTCATAGCTCACTG[A/C]AACCTTGAACTCCCT | 5663 |
rs549955841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73155904 | TGAACCCTAAGGTAA[A/G]CTGTGGACTGTCAAT | 5663 |
rs549972328 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135478 | GTTCAAGCGATTCTC[C/T]TGCTGCAGCCTCCCG | 5663 |
rs549973396 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73170131 | TGTATTATAATTAGC[A/G]TATAGTGAGCAGTGA | 5663 |
rs549975849 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194342 | CTGCAGCCTCAAACC[C/G]TTGTCCTGGGCTCAA | 5663 |
rs549994029 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73199808 | TGGAGTGCAGTGGTG[C/T]GATCTCGGCTCACTG | 5663 |
rs550002014 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186768 | GGCGACAAAGTGAGA[A/C]CCTGTCTCAAAAAAG | 5663 |
rs550022048 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208718 | CCCAGAAAATGCACC[A/G]TAAGTTCTCACTGTG | 5663 |
rs550055242 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222419 | CAGTGTATGTATTCT[C/T]GATATAACTTGTAGA | 5663 |
rs550067518 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221308 | TTATCATTGAGAAAG[C/G]ACAGCTACAGCAAAG | 5663 |
rs550086496 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195655 | GGAGTGAAGTGGCAC[A/G]ATTATAGCTCACTGT | 5663 |
rs550089025 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169256 | TTCCTTCTCCTCTAT[A/T]CTCTTAATCTCGTTT | 5663 |
rs550138815 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148657 | GAGAGCAGAGGCCAG[A/G]CACGGTGGCTCATGC | 5663 |
rs550141411 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73172869 | GTCCAGGCTGGAGCC[C/G]TAGCCTTCATTCTGA | 5663 |
rs550147039 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73139685 | TCAATATCTAACCAG[C/T]ATAAAAATTTACTTG | 5663 |
rs550162338 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73170197 | TTTGGTGGGTTTTGG[C/G]CAGCTTCTTTATTGC | 5663 |
rs550173655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141530 | GAGCACAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 5663 |
rs550223893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208150 | TGAGTCTGGACTCCC[C/T]GAAGGGCCACATCTC | 5663 |
rs550238427 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73214909 | TCTTTGAACGGTGAA[C/G]TTAAAAAGGGTTAAG | 5663 |
rs550275535 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PSEN1 | GRCh38.p7 | 14:73215780 | CAGAGTGGCTAGAAT[A/G]AAAAAGGCTAACAAT | 5663 |
rs550343284 | snp | C/T | 5.13062e-05 | 0.00506463 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73148083 | TCTGAGGACAACCAC[C/T]TGAGCAATACTGTAC | 5663 |
rs550355231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158108 | CACAGTTTTTGATCT[A/G]TTTACTTGTTGGTAG | 5663 |
rs550369474 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73156123 | GTGGATCACTTGAGT[G/T]CAGGAGTTTGAGACC | 5663 |
rs550413121 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73164087 | AGAAGCAGATAGATC[C/G]AGGAGATGTTTTGGA | 5663 |
rs550426619 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204504 | TTTTTGTACAGCTTA[G/T]AAGCTAAAAATGCTT | 5663 |
rs550534396 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192359 | GCTGGGAAGACCACC[G/T]GATCTCCGGAGGTAA | 5663 |
rs550609806 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73218193 | CTAGGTTCAAGCGAT[-/C]CTCCTGTCTCAGCCT | 5663 |
rs550665245 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219618 | GCGTGGTCACAGGAC[A/G]ATTTCACTGACACTG | 5663 |
rs550679159 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73218699 | CCCGCACAGCATAGA[A/G]AAGCCCCCGCACAGC | 5663 |
rs550739639 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158649 | TATTTTTTATAGAAG[A/T]TGGAGTCTTCCTATG | 5663 |
rs550871423 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73176144 | ATAATCTATTAGTAA[G/T]GTATGGAGACCATTA | 5663 |
rs550932939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195069 | TACCTTATGTTGTAT[A/G]GTACTTGATGGTTTG | 5663 |
rs550939871 | in-del | -/TTTG | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73175121 | AGGTCAGGAGTTTTT[-/TTTG]TTTTTTTGTTTTTTT | 5663 |
rs550954569 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73183457 | CGGCCTTCCGCAGTG[G/T]TTGTGTCCCTGGGTA | 5663 |
rs551035471 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73158209 | TTGTATGGGCATATG[C/G]TTTAATTTATCTTGG | 5663 |
rs551070046 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222968 | CTTGGGCTGGAAACT[A/G]TCATATAATCATAAG | 5663 |
rs551094056 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187953 | ATACTTTTTTTTTTT[G/T]AGTCTCACGCTGTTG | 5663 |
rs551170718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168209 | AAAAATACAAAAATT[A/G]GTTGGGCATGGTGGT | 5663 |
rs551207332 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223398 | AATTTTCCTTTTGAA[A/T]TACGTAATTGTTGAG | 5663 |
rs551209945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160012 | ATTTTTTTGTAGAGA[C/T]GAGTTCTCGCCATAT | 5663 |
rs551210001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168657 | ATCCCTTTTTCAACT[C/T]CCCATTCTGCTGAGA | 5663 |
rs551228949 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179396 | CCAAGGCGGGCAGAT[G/T]GCCTGAGCTCATGAG | 5663 |
rs551246692 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160632 | TTTTTCTAATGATTA[C/G]TGATGTTGAGCATCT | 5663 |
rs551248965 | in-del | -/AT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73206811 | AAACTCTCTCCAAAC[-/AT]GTAAAAGTAAGAATC | 5663 |
rs551270493 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206276 | TTGTTGAACAGTCTT[A/G]AGGCAGCATTAGGAA | 5663 |
rs551352249 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73202673 | GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATT | 5663 |
rs551390846 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73173464 | GTGACTTATAAGATA[C/T]GAATTGAATTAAGAA | 5663 |
rs551393986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148617 | GAAATTTGACTGCAA[C/T]TCTACTAGCTAATCA | 5663 |
rs551395826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73140655 | AGACCCTGTAGGGGC[A/G]TTATATAACTTCTGG | 5663 |
rs551462990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73142924 | GTTTGCAGCAGGTGA[C/G]CAGAGAGCAAAAACA | 5663 |
rs551474326 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156732 | CAGTGGCATGATCTC[A/G]GCTCACTGCAAGCTC | 5663 |
rs551512952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73149442 | CAGCAAGATCTGTAG[A/G]GGATTAGTCCGTGAA | 5663 |
rs551583095 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73170475 | TGAAAAAGGTGCTTG[C/G]AGCTGCAGCCAGTAA | 5663 |
rs551597008 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135737 | CATGTACCGTTAATT[C/T]CATTTTCGGTTTTTT | 5663 |
rs551618275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171334 | TCAGGGCCATTGGGC[A/G]CCCATTGCTCTTCTG | 5663 |
rs551633086 | snp | C/G | 0.031825 | 0.122064 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136374 | AGGCCGGAGGCCCCG[C/G]CCCCTTCCTCCTGGC | 5663 |
rs551648073 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73189607 | ACAAGAGTGAAACTC[C/T]ATTTCAAAAAAATAA | 5663 |
rs551657220 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200124 | AGAGATCTAATAGGC[-/A]AAAAAAATAACATCT | 5663 |
rs551696111 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73172371 | GCAGGTGAAGGGCAG[A/G]GGTTAGAACTAGAGG | 5663 |
rs551710381 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73150626 | CAAAATTTAGCCAGG[C/T]GTGATGGCAGGCACC | 5663 |
rs551780641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157322 | TTTTTTTTTTTAAGT[A/G]CAGATGGGGTTTCAC | 5663 |
rs551817377 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73150397 | TTACCATGTTTAATA[A/T]AATTGAGTATTAGGC | 5663 |
rs551902966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73203484 | ACGCAATGCCGATGA[A/G]TACTTTTTCCCTGAA | 5663 |
rs551903081 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195920 | AATTATTTGCCTAAG[A/C]CTAAACTCTGATCTC | 5663 |
rs551905698 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160597 | AGTGGCCATCCTAAC[A/G]GGTGTAGTTTTTTTT | 5663 |
rs551932772 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73172031 | TTTATTGCAAGGCCT[A/G]TGAGGGTACTGAGTC | 5663 |
rs551939737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196736 | GCCTCAGCCTCCCCA[A/G]AGTGCTGGAATTACA | 5663 |
rs551953411 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73146078 | GCCACTACATTGCAG[C/G]CTGGGTGACAGAGCA | 5663 |
rs552050128 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73164270 | GAGTTCTAGGAGAGG[A/T]CAGAGATGGAGATCA | 5663 |
rs552092749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181521 | CCCAGTTACTTGGGA[C/T]CCTGAGACGAGATGA | 5663 |
rs552133556 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73159819 | TATAACATGGACTAC[C/T]TGAGTTTTTTTCTTT | 5663 |
rs552224682 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73142285 | ATACTTTTGTAAAAT[A/G]AAGAATAAATCACAA | 5663 |
rs552237363 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154541 | AGGAGGTCGAGGCTG[C/T]AGTGAGCTGTAATCA | 5663 |
rs552320571 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73188301 | ATATTACTAGATCAT[C/T]ATCTCTGTATGTGCT | 5663 |
rs552354541 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | PSEN1 | GRCh38.p7 | 14:73185536 | TTGCAGTGAGCCGAG[A/G]TGGCAGCAGTACAGT | 5663 |
rs552448113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201158 | CAGTGGGGCGATCTC[A/G]GCTCACTGCAAGCTC | 5663 |
rs552451936 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73207996 | AAGTAAGAAATATAC[G/T]GGAAAGAATTGCCAC | 5663 |
rs552481597 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73144310 | TCCCAAAGTGCTGGG[-/A]ATTACAGGCGTGAGC | 5663 |
rs552485032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201588 | TGGCAGTGGAAGTGA[C/T]GGTGTAGGCAGAGAA | 5663 |
rs552515125 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154432 | CACGATCTTGTCTCT[-/A]ACAAAAAAAAAAGTG | 5663 |
rs552573824 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73213399 | GTCCTCCTCCTCTTC[G/T]TCTCCAACTTTTAAA | 5663 |
rs552586362 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73181453 | AAAATCAATCAATCA[A/G]TCAGTCAATCAATCA | 5663 |
rs552595280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73209023 | CAGTGCTGCCCCAAG[C/T]GCCCGCACACCCGGC | 5663 |
rs552620225 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73151311 | TGCTGCAGTGACATA[C/T]TAATTCATTAGTCTG | 5663 |
rs552627930 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73213812 | ACTTCATACTCACTA[A/G]ATTGGCTATAATAAA | 5663 |
rs552662940 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73207609 | CAGTAAGCAAGGCAG[C/G]AGAACAAGGTCATGT | 5663 |
rs552691012 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221912 | CAAAACCAGCAGTAG[A/G]GTATGACCAGCCAAG | 5663 |
rs552718246 | in-del | -/T | 0.417196 | 0.185864 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160970 | AGATATATGATTTGC[-/T]TTTTTTTTTTTTTTT | 5663 |
rs552810428 | in-del | -/GT | 0.078151 | 0.181571 | intron-variant | PSEN1 | GRCh38.p7 | 14:73191398 | TATGTGTATGTATAA[-/GT]GTGTGTGTGTGTGTA | 5663 |
rs552851649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196166 | ATTTTCAAAGCAAAA[A/G]CAATTTTAATTTAAT | 5663 |
rs552864532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73147888 | AAAGGTTTGTTTCTG[C/T]TTAATGTAATCTATG | 5663 |
rs552941035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73164240 | ATGGAGAAGACAGAG[A/G]AGAAGCTTAGAATAG | 5663 |
rs552954017 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135389 | TTATTTTTTAATTTT[A/T]ATTTTTATTTTTTGA | 5663 |
rs552975700 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73182879 | AAAAGAAATAAATAA[A/G]AACATCTCCTTCTTC | 5663 |
rs552984671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73189360 | TCATGCCTGTAATCC[C/T]AGCACTTTGGGAGGC | 5663 |
rs552985147 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73139981 | TACAAATTAATTAGA[C/T]GTAAATAATCATTTT | 5663 |
rs553013941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156218 | GTAATTAACTGGGTG[C/T]GGTGGCATGTGCCTA | 5663 |
rs553079999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156953 | AGGCATGAGCCACCA[C/T]GCCTGGCCTTTTTTT | 5663 |
rs553188425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73176954 | CTCCATGGAAACTGC[A/G]TATCATGTGGTTACC | 5663 |
rs553189487 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73149849 | TCAAATAGAAGATAA[C/T]ATCTAAAGCATTTCT | 5663 |
rs553228618 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73150590 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAA | 5663 |
rs553261933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73189911 | GGGTGGGCACTGAGC[A/G]GTAGCAGGTGTAGAC | 5663 |
rs553263464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143092 | CCTAGTGTCTTTTGC[C/T]ACGCTGCCTGAACAG | 5663 |
rs553271052 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73151844 | AAAGTGCTGGGATTA[C/T]AGGTGTGAGCTACTG | 5663 |
rs553312969 | snp | C/T | | | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73223916 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 5663 |
rs553331021 | snp | A/G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136159 | AATAGGTACCCTAAA[A/G/T]AAATGACAGGTGTTA | 5663 |
rs553348480 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73203039 | TAAATGTCTGGTGAA[C/G]ATTTGAGGATTTTAT | 5663 |
rs553408002 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181782 | TTTATTTTGTTTCGT[A/T]TTTTTTTTTGAGACA | 5663 |
rs553511016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73165913 | ATACAAACATTAAGC[C/T]GGCGCAGTGGTGGAT | 5663 |
rs553546038 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158277 | GGTGTATATTTAACT[A/T]TTTTTTCTATCTATC | 5663 |
rs553580587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211054 | TTGTCACCAAATCCA[A/G]GGATGAGTGCCAACA | 5663 |
rs553582848 | in-del | -/A | 0.0130921 | 0.0798413 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179477 | AAAAATTAGCCAGGC[-/A]ATGGTGGTGGGCACC | 5663 |
rs553596502 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221581 | CAGTGTACAGAGAAC[C/T]TATCTTTCCTTTTTT | 5663 |
rs553688923 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204670 | AGGAGCTTGTAGCTA[G/T]ATTTTTTCATACTTG | 5663 |
rs553691585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73161794 | TGTGACACAAGGCCC[C/T]CACCGTAGATCACAT | 5663 |
rs553723390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205113 | CAAGAAGCCTGAGTA[C/T]TAGAAACATGGATAA | 5663 |
rs553723699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197378 | TTCAGCACCACATAC[A/G]TATGTTCTGAGACCT | 5663 |
rs553736950 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73155153 | GTGGCAGTAATCTCA[A/G]TCTTTATCATTAATT | 5663 |
rs553773636 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148189 | AGAAATGCTGAGGGG[A/G]CTAGGCAGGCTTTCT | 5663 |
rs553797300 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73165385 | AAACGATTCTCCTGC[A/G]TTAGCCTCCTGAGTA | 5663 |
rs553801418 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73197812 | TCAAACCCAAATGAA[A/G]TTTTTACAGATGTTC | 5663 |
rs553804789 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73220712 | GTCTCTGCCCGCGTT[A/G]CCTTTCCTCTCAATG | 5663 |
rs553820765 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162489 | GAGAGAGAGAGAGAG[A/C]GAGAGCACGCGAACA | 5663 |
rs553898801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73176880 | ACACATAGCTATTAC[A/G]TAAGATTCCTCTCAA | 5663 |
rs553968596 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194657 | CACTGCAAGCTTCGC[C/T]TCCCAGGTTCATGCC | 5663 |
rs553973095 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162996 | GCTTTGCCTGCTTTT[A/G]AACAAATAAATTGTA | 5663 |
rs554020121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139821 | GTAAATGTTTGTTGA[C/T]TGAAAGATATTAATA | 5663 |
rs554039014 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179542 | GTATTGCTTGAACCC[A/G]GGAGGCAGAGGTTGC | 5663 |
rs554041116 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PSEN1 | GRCh38.p7 | 14:73203899 | CCAGGCATGACTATA[A/G]TCCCAGGACTTTGGG | 5663 |
rs554092907 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73207696 | GGTGGCACCTTTTCC[G/T]GAGATTTGCTCAGGC | 5663 |
rs554126878 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158254 | GTAGAATATGATCCA[A/G]TATGGTAGGTGTATA | 5663 |
rs554175516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216132 | CCAAGAAACTGTAGA[C/T]ACATGCAGTATCATG | 5663 |
rs554248045 | snp | A/G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136404 | CTCCTCCCCTCCTCC[A/G/T]TGGGCCGGCCGCCAA | 5663 |
rs554259970 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195270 | CTCTCCCTCCCGGGA[G/T]CAAGCGATTCTCCTG | 5663 |
rs554265638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73191101 | TTTGCCTCCCCAGAA[C/T]TAAAATAGCATTTTC | 5663 |
rs554298277 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73191717 | AACTTTAGCTAATTT[A/T]AAAATTTTTTTGTAG | 5663 |
rs554299058 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187991 | TGGAGTGCAGTGGCA[G/T]GATCTCGGCTCACTG | 5663 |
rs554310525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197034 | GCTTCCCGGGTTCAC[A/G]CCGTTCTCCTGCCTC | 5663 |
rs554368425 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73217430 | ATTAGAATCACTTGG[G/T]AGCTTTTAAAACTGT | 5663 |
rs554376378 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73159831 | ACTTGAGTTTTTTTC[-/T]TTTTTTTTGATGACA | 5663 |
rs554458653 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223662 | CAGATTTTCTGTATT[C/T]GTCAGATTAATAAAG | 5663 |
rs554461749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73144708 | TTAGTTTAATAATGT[C/T]TCTAAGTTTTACATA | 5663 |
rs554590654 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212151 | GAGTCTCGCTCTGTC[A/G]CCAGGTTGGAGTGCA | 5663 |
rs554605830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143851 | CTTTCTCTAAATAAA[A/G]AACTAGCCACCCATG | 5663 |
rs554628070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197283 | AAAGTGCAGTTGATC[A/G]AAAGAAATGGTGGTA | 5663 |
rs554647962 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205788 | TGAACTAAAATGTGG[A/T]AGAGATGCACATGTG | 5663 |
rs554677652 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168362 | TCTGTCTCAAAAAAA[A/C]AAAAACAAAAACAAA | 5663 |
rs554744599 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136586 | CGGGGAAGCGTATGT[G/T]CGTGATGGGGAGTCC | 5663 |
rs554783173 | snp | A/C/G/T | 6.67497e-05 | 0.0057768 | synonymous-codon, missense | PSEN1 | GRCh38.p7 | 14:73206438 | CCCGGAAGCTCAAAG[A/C/G/T]AGAGTATCCAAAAAT | 5663 |
rs554858864 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219395 | AACAAAGTCAAGATT[C/T]CCGGCTGGACTTTTG | 5663 |
rs554919330 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73167430 | AAATATTCCAAAATG[A/C]AAAATCTGAAACACT | 5663 |
rs554921039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73146296 | GGACTCAAGCCATCC[C/T]CCCACCTCAGCCTCC | 5663 |
rs554974712 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73215475 | GTAATCCCAGCTATT[C/T]GAGAGGCTGCGGCAG | 5663 |
rs554982388 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194687 | CGTTCTCCTGCCTCA[A/G]CCTCCCAAGTAGCTG | 5663 |
rs554996321 | in-del | -/AAAGG | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173874 | ATTCAAAAAATACAA[-/AAAGG]AAAGGAAGCCAGGTG | 5663 |
rs554999774 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73177932 | TTTTTCAACCATTAT[G/T]TCTTCAAAATTTTTC | 5663 |
rs555030615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200861 | TTTGAAACCAGCCTG[A/G]CCAACATGGTGAAAC | 5663 |
rs555049436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208988 | CCAGAGGGGGCCAAG[A/G]TGGCAGGGGGCTGGC | 5663 |
rs555056057 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222489 | GGGTTAGATGACTGC[A/G]GGAAGCCTTTGATCC | 5663 |
rs555136184 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73156663 | CCATAATAAAAAGTT[G/T]TGTTTGTTTTTTTTT | 5663 |
rs555150760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160129 | ATGCCCAGCTGGCTA[A/G]ATATTTCATGTAAGT | 5663 |
rs555183416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152964 | AAGAGGATTGGTTTC[A/G]AGGTTCACCTGGGAG | 5663 |
rs555187174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73199196 | GTTTAGAAATGAAAT[A/G]CTAGAGCTTGGGAAA | 5663 |
rs555201705 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73138523 | CCTGCCCGGCCGGCT[A/G]TTTATTTTTTTAGAG | 5663 |
rs555292516 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148890 | GTGAGCTGACGTCGC[A/G]CCATTGCACTCCAGC | 5663 |
rs555314845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73202077 | TTGAGGTAAGTCTTG[C/T]TCTGTTGCCCAGGCT | 5663 |
rs555329078 | in-del | -/TC | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73181270 | CATGGAGAAATCCTG[-/TC]TCTACTAAAAATACA | 5663 |
rs555344557 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73165916 | CAAACATTAAGCCGG[C/T]GCAGTGGTGGATGCC | 5663 |
rs555351933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195352 | TAATTTTTGTATTTT[C/T]AGTAGAGACGAGGTT | 5663 |
rs555548728 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73163227 | CTCCCAGGCACACCT[A/T]CATGGTGCTTCATTT | 5663 |
rs555555713 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73202826 | GCTTTAGCAGCACAT[A/G]ATAGTAAAATTGGAA | 5663 |
rs555608494 | in-del | -/A | 0.295088 | 0.245901 | intron-variant | PSEN1 | GRCh38.p7 | 14:73214531 | GCGAAACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 5663 |
rs555616411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156863 | GAGATGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 5663 |
rs555617277 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171773 | ACATTGCTTTACGAG[C/G]AAGTTAAGTTTAAAA | 5663 |
rs555648829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195972 | TATTCTTTTCACCGT[A/G]TTACAATATTTTTAC | 5663 |
rs555656308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73164335 | GCCGACGATTTTCTA[C/T]TGATAGACTAAAAAT | 5663 |
rs555685027 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157656 | CCCATCCCCAGGCAA[C/G]CATGTTTTGTCACCG | 5663 |
rs555731901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137577 | GAGGAGGCCAAGGCA[A/G]ACACTTAGGAACACT | 5663 |
rs555859211 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73201535 | TCCAAAGGGAAGGTG[C/T]GTATGTGTGCATGCA | 5663 |
rs555895778 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73189879 | TGACCTTTACCATGT[G/T]TTGGTCTCCCTTGAC | 5663 |
rs555895920 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73180622 | TATACATAATTTGTT[A/T]TAAAAGGAACTATAA | 5663 |
rs555932531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181175 | CTGGGCGTGGTGGCT[C/T]ACGCATGTAATCCCA | 5663 |
rs555938026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73165123 | CACCACACTGGCTAA[C/T]TTTTGTATTTTTAAT | 5663 |
rs555987907 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216576 | CCAGCCTGACCAACA[G/T]GGTGAAACCCTGTCT | 5663 |
rs556049537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73176724 | GCCTTGTTTTAATTA[A/G]ACACTAGTTCTTTGA | 5663 |
rs556059607 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73218131 | GAGTCTTGCTCTGTC[A/G]CCCAAACTAGAGTGC | 5663 |
rs556061647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210310 | GTATATTCTGGCTAT[A/G]GCAAAGTAGTTTAGT | 5663 |
rs556078383 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167929 | ACCTTGATACAGAAG[A/G]GCTGGGCTCCTGGCT | 5663 |
rs556100454 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210989 | ATAAAGACATTCACT[A/C]CCCGCTCCTTTCCCA | 5663 |
rs556147068 | snp | A/G | 3.29527e-05 | 0.00405898 | missense | PSEN1 | GRCh38.p7 | 14:73192661 | AAGTGTTTAAAACCT[A/G]TAACGTTGCTGTGGA | 5663 |
rs556171721 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73217332 | AGTTCTGTTTTAACC[C/G]CAGGTGGGTTAAATA | 5663 |
rs556193070 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73165907 | CTAAAAATACAAACA[-/T]TAAGCCGGCGCAGTG | 5663 |
rs556254447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193896 | TCTTGGGCTCAAGCA[A/G]TCCTCCTACCTTGGC | 5663 |
rs556259919 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73175839 | GGGCAAATTATCTAC[A/G]TATTTATAACTGTCT | 5663 |
rs556287832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73165410 | TGAGTACCTGGGACT[A/G]TAGGTATGTGCCACT | 5663 |
rs556289551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194629 | ACTGGAGTGCAGTGG[C/T]GTGATCTTGGCTCAC | 5663 |
rs556299654 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186553 | AGTCTGAGGCGGGCG[G/T]ATCACTTGAGGTCAG | 5663 |
rs556326451 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73142486 | CAGTAGAAATTTTGT[G/T]TATATTTATGTCTGA | 5663 |
rs556332591 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73215257 | TGAGCCACTGTGCCC[A/G]GCCAAAAAAATTTTT | 5663 |
rs556401968 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195298 | CTGCCTCAGCCTTCC[A/G]AGTAGCTGGGACTAC | 5663 |
rs556460917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73213310 | ATAATAGTTGTTGAC[C/T]AGAGCAGCAGCATAA | 5663 |
rs556537775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73146750 | TCCTGATGTTAAAAG[C/T]GAAAATGAAATAGGA | 5663 |
rs556560166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200328 | AAGCTGGAGTACAGT[A/G]GCGCAATCTCAACTC | 5663 |
rs556576532 | in-del | -/TAA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73188358 | CTTGATCAGATTCCT[-/TAA]TAAATAGACGGGGTC | 5663 |
rs556660751 | in-del | -/TTTTTTT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73212123 | TTTTTTTTTTTTTTT[-/TTTTTTT]GAGACAGAGTCTCGC | 5663 |
rs556688457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73190220 | AGGCTGGGTGTGGTG[A/G]CTCACACTTGTAATC | 5663 |
rs556789528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139815 | AACCCAGTAAATGTT[C/T]GTTGATTGAAAGATA | 5663 |
rs556813523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73178108 | AATTTTTAGTAGAGA[C/T]GGGGTTTTACCACAT | 5663 |
rs556896277 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73186717 | AGGAGGCAGAGGTTG[C/T]GGTGAGCTGAGATCG | 5663 |
rs557003107 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73219050 | CAGTTAACTATGTTA[A/T]AAACCAAGACTTGTG | 5663 |
rs557032981 | in-del | -/AAT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73207149 | ATACCTTACCTCAAA[-/AAT]AATAATAATAATAAT | 5663 |
rs557077759 | in-del | -/TTTTTCTTACA | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73203419 | ACAGAATGTAAGAAT[-/TTTTTCTTACA]TTTTTCTTACATTTT | 5663 |
rs557139255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211177 | GAGGTGTAGGCATTT[A/G]AAATTTGTAGGGTTG | 5663 |
rs557189118 | in-del | -/AGT | 0.00358779 | 0.0422022 | intron-variant | PSEN1 | GRCh38.p7 | 14:73175811 | GGGTAAAATCCTAGA[-/AGT]AGAATTTTTGGGGCA | 5663 |
rs557220442 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136205 | TCGCTTGTATGCCGG[A/G]AGAAGCACACGCTGG | 5663 |
rs557236926 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73139157 | ACATGGTGCCAGGCA[C/T]TTGTAGTCCCAGCTA | 5663 |
rs557247957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181804 | TTTGAGACAATGTCT[C/T]ACTTTGTCAGTCAGG | 5663 |
rs557288733 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173470 | TATAAGATACGAATT[C/G]AATTAAGAAAAAGAA | 5663 |
rs557305252 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73203331 | GACCTCAGGTGATCT[A/G]CCCGCCTCACCCTCC | 5663 |
rs557343419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73174732 | AAACTCACTGGTGAC[C/T]GGTCACACCTTGCCT | 5663 |
rs557402516 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222392 | ATTACTTGTTATTTA[C/T]GTGGCCTCAGACAGT | 5663 |
rs557409892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205157 | AAAAGCCAGAGAGAC[A/G]TAAATGTCAAGTATC | 5663 |
rs557458255 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73171197 | AGCAGTTGAGAGAGC[A/G]AGGGGTTATTACTTC | 5663 |
rs557521528 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200826 | GAGGCCTAGGTGGGC[A/G]GATCACTTGAGGTCA | 5663 |
rs557528526 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PSEN1 | GRCh38.p7 | 14:73167227 | AAAGTCACTCCCATG[A/G]TAACTAACCTACTCC | 5663 |
rs557572509 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205170 | ACATAAATGTCAAGT[A/T]TCTTGTTTAAAATTA | 5663 |
rs557577799 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73196933 | TCTTTCTTTCTTTCT[-/T]TTTTTTTTTTTTTTT | 5663 |
rs557581715 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148207 | AGGCAGGCTTTCTCT[A/G]CTTTACCACATTTAT | 5663 |
rs557586590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73144983 | CTGCAACCTCCACCT[C/T]CCAGGTTCAAGCGAT | 5663 |
rs557649513 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162454 | GCTCGCGCGCTCTCT[A/C/T]TCTCTCTCTCCATGA | 5663 |
rs557701527 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192039 | ATTTTTATAGTTATG[G/T]CCTGTGCAACTGGTT | 5663 |
rs557715058 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208266 | CAATCCTGCCATTCA[A/G]TGGGTCCCAAGTTCT | 5663 |
rs557739432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73178831 | TTGGCCAATTGATCT[A/G]ATTGGGCTAGGTCCA | 5663 |
rs557753040 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73177830 | GTTTAATTATGGGAC[C/T]GTGTGAGGATTTCTT | 5663 |
rs557755410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141683 | CTAGCTACTCAGGAG[A/G]CTGAGGCAGGAGAAT | 5663 |
rs557786557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168836 | GCACCTGGCCATCCC[C/T]GAATGGCCGCGTTGA | 5663 |
rs557806863 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73214264 | CTGGGCGCAGTGGCT[C/G]AAGCACCTGTAATCC | 5663 |
rs557831165 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134994 | TTCACAAATAGATGG[A/G]TTTTAGCCTGTATTT | 5663 |
rs557878381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73161820 | CACATTATTAGCGGA[A/G]ACTTGTTGGCATGAC | 5663 |
rs557910624 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220223 | TTTCTACAGCCAGTA[A/G]GGCAGCTCTGTCGTG | 5663 |
rs557927352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169873 | CTGGTCTCAAACTCC[C/T]GACCTCAAGTGATCT | 5663 |
rs557959863 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73188055 | TGCCTCAGCCCCCTG[A/T]GTAACCGGGACTACA | 5663 |
rs557998511 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179676 | TAGGAGACCTCTTTC[C/G]TGATCCTCAAGCCAG | 5663 |
rs558018349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208912 | GGGTGCCTGCAGGCC[C/T]ACGGTAAGCTGCCTT | 5663 |
rs558107191 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194729 | ATCTGCCACCACGCC[A/C]GGCTATTTTTTTGTA | 5663 |
rs558115765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152088 | GGCTAATTTTTTGTA[C/T]TTTTCATAGAGGCGG | 5663 |
rs558115853 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73144186 | GCTGGGACTACAGGT[C/G]CACGTCACCATGCCT | 5663 |
rs558169263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73209758 | AGTGGTAATAGGGGA[C/T]GGCCCGCTGAAGGAT | 5663 |
rs558296580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73180535 | TGGTTGGTTATGCAA[C/T]GTCTGTGGCAAGCCC | 5663 |
rs558328183 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162529 | GTGAGAGAGAGAGCA[C/T]GTATCTGCAGTCTCA | 5663 |
rs558360296 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73174062 | AAAAATTAGTGTAAA[-/AT]ATATATATATTATGA | 5663 |
rs558401935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192557 | GGGATATTAATATCT[A/G]ATGTTTGGGAGCCAT | 5663 |
rs558418546 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73223861 | GAGAATCGCTTGAAC[C/T]CAGGAGGCAGAGGTT | 5663 |
rs558434473 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73184421 | CCCTCTCCGACGGGG[C/T]GGCTGGCCTGGCAGA | 5663 |
rs558466146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168428 | CTGACGTCAGGGATA[C/T]AAATGGCTGTGTGTT | 5663 |
rs558471553 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73138307 | CACTGCAAGCTCCGC[C/T]TCCCGGGTTCACGCC | 5663 |
rs558507613 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168763 | ACACTGGAAGAGAAC[A/C]TGGGTGCCAAGAGGA | 5663 |
rs558529343 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73177060 | TATTGCCTCCCACTT[C/G]ACACTGATTCTGGCT | 5663 |
rs558544799 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73214843 | AAGATGAAAAGAGTT[A/C]TGTGGATGGACGATG | 5663 |
rs558584625 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137285 | AAGAAACACTAACGG[A/G]ACATGGGAACCAATT | 5663 |
rs558647571 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73182853 | CCCAAAAATAAATAA[A/G]TAAAATTAAAAAAAG | 5663 |
rs558733563 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73153983 | CCTCTCAAAGTGTTG[A/G]GATTACAGGCATGAA | 5663 |
rs558739735 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73180873 | ATTGACTTTGTCAAG[A/G]TTAGTCTTTTTTGTC | 5663 |
rs558825875 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212641 | GCTATATTTTATTTT[A/T]AAGAAAATCAAAGGG | 5663 |
rs558898126 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73220627 | AGCAGCGAAGGGGAT[A/T]CAGTGAGCTAATGAT | 5663 |
rs558906462 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186271 | TAATCCCAGCTACTT[-/G]GGGGGGCTGAGGCAG | 5663 |
rs558969058 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201444 | AAGTAAAACCATACA[C/G]TATTTGCTGTCTAAG | 5663 |
rs559015884 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186513 | CGGGCATAGTGGTGC[A/T]CATCTGTAATCTCAG | 5663 |
rs559021045 | in-del | -/ACTC | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179506 | CCTGTAGTTCCAGTT[-/ACTC]AGGAGGCTGAGGCAG | 5663 |
rs559028030 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73156827 | GCCACCATGCCCAGC[C/T]AATTTTTTGTAATTT | 5663 |
rs559067827 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193359 | TTGACAAGCTGGCCA[A/G]TATGGTGAAACCCCG | 5663 |
rs559193105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73185902 | CTAATGGATGAGGAG[C/T]TAGACAGAAATTTTA | 5663 |
rs559221214 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73147198 | GCCATGTTGGTCAGG[A/C]TGGTTTCGAACTCCT | 5663 |
rs559232223 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141318 | TGGGATGGAAGGAGA[A/G]AAAAAAAAAATCACC | 5663 |
rs559257889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139595 | AAAAAAAGAAAAAAA[A/G]GGGGGGCAAAAAGAA | 5663 |
rs559343267 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223363 | TGTGTCTGTGTAGCA[A/G]GGACGATTTCCCAGA | 5663 |
rs559345960 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73169141 | AACTTCCCATTGTCA[A/G]TTCAGGGTCTTTTTA | 5663 |
rs559364832 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73155511 | TATATTATCATTATT[A/T]TTTTTTTTTTGAGAC | 5663 |
rs559453059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73188312 | TCATCATCTCTGTAT[A/G]TGCTAAAAGGCATTT | 5663 |
rs559455884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73163632 | AAAACCAGATCAACG[C/T]AGAGAAAGGCTTCCT | 5663 |
rs559485868 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141806 | GGTGCCGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 5663 |
rs559498366 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73150302 | AGTTATATGACAAAA[A/C]ATTGCAGATAAAATT | 5663 |
rs559535261 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73150928 | CAAAAATTAGCTGGG[C/T]GTGGTGACACGCGCC | 5663 |
rs559538102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148994 | GAAAAGAGAGAGAGC[A/G]TGGATGTCCTGTGAG | 5663 |
rs559571258 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73175229 | CCTCCTGGGTTCAAG[C/T]GATTCTTCTGCCTCA | 5663 |
rs559580270 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73142489 | TAGAAATTTTGTTTA[C/T]ATTTATGTCTGAGAG | 5663 |
rs559608553 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73178999 | ATATCCATACTCACT[C/T]ACCTTGGGAATGGAC | 5663 |
rs559637505 | snp | G/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221284 | CTCAGACATGTGCTA[G/T]CATGGGTATTATCAT | 5663 |
rs559715028 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73180774 | GGGATTTTTGCAAGA[C/T]GAGAAAGGCCTGTTG | 5663 |
rs559715033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171209 | AGCGAGGGGTTATTA[C/T]TTCATGTTTTAAGTG | 5663 |
rs559722991 | in-del | -/TG | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73175965 | TTTCTTTTTTAAAAC[-/TG]TGCTGGTTTTTATAG | 5663 |
rs559836384 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157224 | TCTGCCTCCTGGGTT[C/T]AAGCGATTCTCCTGC | 5663 |
rs559895662 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73203457 | TTTTTAACAGAATGT[A/G]AGAAAACCACAACGC | 5663 |
rs559925690 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73139267 | CAGCCTGGGCAACAG[A/C]GTGAGACTTCGTTTT | 5663 |
rs559988409 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168553 | AGACTATGGATGGGA[C/T]GTGGCTAACTTCAGA | 5663 |
rs560052122 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73167879 | CCTTTACCTTCTCAG[C/T]TCTCAGTTATTTTCC | 5663 |
rs560079238 | in-del | -/A | 0.257732 | 0.24988 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152441 | CCCATTTCTACTAAG[-/A]AAAAAAAAAAAAAAA | 5663 |
rs560091980 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137685 | GTCGCCAGAGCTGAG[A/G]AAGGGGAGGGAAGCT | 5663 |
rs560207075 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186653 | GTGGTGGCGCGCACG[C/T]GTGGTTCCACCTACT | 5663 |
rs560207155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73177055 | TTATTTATTGCCTCC[C/T]ACTTGACACTGATTC | 5663 |
rs560208504 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193536 | GCCTGGGTGACAGAG[C/T]GAGACTCTGTCTCAA | 5663 |
rs560242968 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73178468 | GCTGGGATTACAGAC[A/G]TGAGCCACCATGCCT | 5663 |
rs560259805 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212781 | AAAGCCCTTTGGTTA[C/G]GGCTCAGTCATCTCT | 5663 |
rs560265370 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160998 | TTTTTTCGATACAAG[G/T]TTTTACTGTGTCACC | 5663 |
rs560296547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205970 | TAAAAATGAGACATA[A/G]TATGAAGGAAATTTA | 5663 |
rs560337173 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151677 | GTCTCAAGTGATCCT[A/G]CCACCTCAGCCTCCC | 5663 |
rs560342467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73199675 | TGCCATATTGCCTCC[C/T]AAAAAAGCTGTGCCT | 5663 |
rs560387944 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73207903 | CAGCCTCAGGTACTA[G/T]CTCCCTGCTGCAGCT | 5663 |
rs560420877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208502 | AGTGGAGAGGAGACC[C/T]GGAATGGGTATCTCC | 5663 |
rs560433382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206818 | CTCCAAACATGTAAA[A/G]GTAAGAATCTCCTAA | 5663 |
rs560448251 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169555 | TGTTCCATTGTGTTC[C/T]TTATCTCTACCAATG | 5663 |
rs560449246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73174577 | GTATACTGAAGAAAT[A/G]TACTCTAAGACCTTT | 5663 |
rs560455045 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193975 | ATTCACTTTTAAAAT[C/G]AAAATTAGGTTACCT | 5663 |
rs560556392 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139872 | AGGAAAAAGGTATTA[G/T]TATTGGCTTTTCACA | 5663 |
rs560558938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73214586 | AAAAATGTCTTACAT[C/T]TCTAATTAAAATTTT | 5663 |
rs560595334 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PSEN1 | GRCh38.p7 | 14:73189495 | TGGGTGCCTGTAATT[C/T]CAGCTACTCTGGAGG | 5663 |
rs560630555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181055 | ATTAAAATTGGGGAA[A/G]GAAAGGGAAAACAAT | 5663 |
rs560650416 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73191149 | TAACATTCATTGTTT[C/T]TTTAAAAAAGACATT | 5663 |
rs560693858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205818 | GTATATCTAGATCTA[A/G]ATTGATATATTGATA | 5663 |
rs560741389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73170047 | GACCATACAAGGTAA[C/T]TTCCGGACGTTGCCA | 5663 |
rs560757645 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73163426 | CTACAAAAAATTAGC[C/T]GAGCTTCACAAACAA | 5663 |
rs560780088 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136238 | CCAATTTATATAGGG[G/T]CTTTCGTCCTCAGCT | 5663 |
rs560820843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210625 | CTGCTGTTTTCATTT[A/G]TAAATCTTATTCTTA | 5663 |
rs560857524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211413 | TTTCCCAGGAATCCC[A/G]GTGGACTTTGCTTCA | 5663 |
rs560885666 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73213274 | CTTTTCTCACAGGCA[A/C]CAGGAGCCAGAGGAA | 5663 |
rs560887568 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135529 | CGCGCCACCACACCC[A/G]GCTAATTTTTTTGTA | 5663 |
rs560998577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73218569 | TCATAAATAAACTTT[C/T]AGTTTATTTTATTTT | 5663 |
rs561032572 | snp | A/C | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204415 | TTTAGGACTATTTAA[A/C]AAATATACTATTTAT | 5663 |
rs561056495 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73214998 | GAGACAATTTCGCTC[A/G]TTGCCTAGGGTGGAG | 5663 |
rs561060686 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73166151 | CTGTTAAGTTAAACA[C/G]TGTTCTAGTATCCAT | 5663 |
rs561093474 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73172618 | GCACAGTTGAGTGTT[C/T]GCACTGGAGACCATA | 5663 |
rs561102761 | in-del | -/TT | 0.0376037 | 0.131863 | intron-variant | PSEN1 | GRCh38.p7 | 14:73177967 | CCACATTCTTTACTC[-/TT]TTTTTTTTTGAAACA | 5663 |
rs561172541 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217828 | TTTGAGACGGAGTCT[C/G]TGTCACCCAGGCTGG | 5663 |
rs561240559 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158360 | GGAGTTTTGCTCCAT[A/C]TGGAGCAAAGGCTGG | 5663 |
rs561326452 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73175124 | CAGGAGTTTTTTTTG[-/T]TTTTTTTGTTTTTTT | 5663 |
rs561339071 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73214355 | AACCAACATGGAGAA[A/T]CCCCACCTCTACTAA | 5663 |
rs561413591 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PSEN1 | GRCh38.p7 | 14:73147201 | ATGTTGGTCAGGCTG[A/G]TTTCGAACTCCTGAC | 5663 |
rs561417189 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152164 | TGATTCGCCCGTCTC[A/G]GCCTCCCAAAGTTTT | 5663 |
rs561453067 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73191281 | CTCTCACACTACTTT[G/T]CATAAATGGGATCAT | 5663 |
rs561480637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73144493 | CTAGTAATCAAAATC[A/G]CTTCAAAATACCGTA | 5663 |
rs561587777 | snp | G/T | 0.0333695 | 0.124785 | intron-variant | PSEN1 | GRCh38.p7 | 14:73184741 | GCTGGCCTGGCGGGG[G/T]GCTGACCCCCCCCAC | 5663 |
rs561638393 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154306 | CACACAATTATAAAC[G/T]TAATTGCAGAGCTAG | 5663 |
rs561642378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73161892 | GGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 5663 |
rs561649636 | snp | A/C | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135133 | GAACAAACTAAAATC[A/C]CTACTCTTGTTAAAG | 5663 |
rs561674765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154727 | TGAAATTAAAAGGAA[C/T]ATGAACAACTTAACT | 5663 |
rs561715468 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73140388 | GCTAATTTTTGTATT[C/T]TTAGTAGAGGTGGGG | 5663 |
rs561732998 | in-del | -/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73218040 | TGATGTGCCTGCCTC[-/G]GCCTCCCAAAGTGCT | 5663 |
rs561769663 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73196994 | CTGGAGTGCAGTGGC[A/G]CAATCTCGGCGCACT | 5663 |
rs561770478 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194395 | CAAAGTAGATAGAAC[G/T]ACAGGCATGCACTAC | 5663 |
rs561787836 | in-del | -/C | 0.0603597 | 0.1629 | intron-variant | PSEN1 | GRCh38.p7 | 14:73184852 | CACTTCCCAGACGGG[-/C]GCGGCTGCCGGGCGG | 5663 |
rs561824740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201377 | AGGCGTGAGCCACCG[C/T]GCCTGGCCGAGAATA | 5663 |
rs561840061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162821 | TTGCTTGCATATGTA[A/G]AAAGAAACTTTGAAA | 5663 |
rs561884041 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73172734 | AAATAATGCACATAC[G/T]TTCTCTCTCATAGAG | 5663 |
rs561892265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73170275 | TTCCTATCTCATCCC[A/G]TAACTAAGAGTACCT | 5663 |
rs561893572 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73216338 | CAATGGACATGTGGA[C/T]TGTGATGATAGTTAA | 5663 |
rs561905167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148324 | ATATCACCACCTCAG[C/T]TGAAGCCTTCTCCAG | 5663 |
rs561932540 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222817 | AGAAATCAATCCATT[C/G]AGTAAAGTACTCCTT | 5663 |
rs561946279 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187619 | CTAAAGAGAGAATAT[A/C]TAAACAGAGTAAAGA | 5663 |
rs561962337 | snp | G/T | 1.65146e-05 | 0.0028735 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192910 | ACAGGAATGCCCCAC[G/T]GGAGTGTTTTCTTTC | 5663 |
rs562065835 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73149714 | AGTAGGATCAAGTCA[A/G]TTGTCTACCAGAGTA | 5663 |
rs562067703 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216346 | ATGTGGATTGTGATG[A/T]TAGTTAAATTGTACA | 5663 |
rs562099274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73215835 | AAAACTGGAACTCTC[A/G]ATTGTTGCTGGTGGA | 5663 |
rs562136139 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216210 | TTGTATGAGTCATAT[A/G]AAATGTCTAGAAAAG | 5663 |
rs562147547 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223232 | TGCTGAAATGAACCC[C/T]TTTCTTGAACATCAA | 5663 |
rs562149399 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73146341 | TACAGATGCATCCCA[A/C]CTGCACCCAGCTAAT | 5663 |
rs562150930 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | PSEN1 | GRCh38.p7 | 14:73149323 | AGAGAGGTTCTGTGT[G/T]TTTTTTTTTTTAATT | 5663 |
rs562173745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73202565 | GCAAGCTCCACCTCC[C/T]GGGTTCACGCCATTC | 5663 |
rs562239623 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73204044 | GCTCTCATTGCCCAG[C/G]CTGGAGTGCAATGGC | 5663 |
rs562258439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73209286 | CCTCCCCTGCTGCAG[C/T]TGCCATCTTTGCAGC | 5663 |
rs562277793 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73167764 | TTTTTGTCTTCATTT[A/C]TGGTGGGGTTGGATA | 5663 |
rs562290636 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141936 | GCCAGGCGTGGTGGC[A/G]GGCACCTGTAGTCCC | 5663 |
rs562315927 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73159613 | ACTGAAGTGCCTTTG[A/T]ACCTTTGCAAAAATC | 5663 |
rs562353206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160307 | AGTAGACATTTGGGT[C/T]ACTTCCACTTCGTGG | 5663 |
rs562374809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73203316 | TGGTCTCAAACTTGT[A/G]ACCTCAGGTGATCTA | 5663 |
rs562376197 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157740 | CCGGGCACGGTGGCT[C/G/T]ATGCCTGTAATCCCA | 5663 |
rs562411635 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196553 | ATCTTGGCTCACTGC[A/C]GCCTCCACCTCCAGG | 5663 |
rs562425953 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73149321 | TAGAGAGGTTCTGTG[-/T]TTTTTTTTTTTTTAA | 5663 |
rs562450338 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73150115 | CATACAGAAAGTATG[G/T]CACATAATGTAATAG | 5663 |
rs562481752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73218750 | GCATAGAGAAGCCCC[C/T]GCACAGCATAGAGAA | 5663 |
rs562484429 | in-del | -/TCTT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73158187 | ATATTCATGTACAGA[-/TCTT]TCTTTGTATGGGCAT | 5663 |
rs562584657 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193039 | ATTTCGGCTGGGCAT[C/G]GTAGCTCATGCCTGT | 5663 |
rs562608051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205888 | TGACTATCCCTATTA[C/T]GTTTATTGCTTTTAA | 5663 |
rs562619386 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193404 | ACAAAAATTAGCTGG[C/G]TGTGGTGGCGTACCC | 5663 |
rs562625477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73185313 | CACTCCAGCCTGGGC[A/G]CCATTGAGCACTGAG | 5663 |
rs562635464 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73176512 | CCTGTGTAGTTGGAT[A/G]GGTGGAGCTCTGGAC | 5663 |
rs562644299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73199498 | CTTACGTAGATATTC[A/G]GTGGTGGGTATCCTC | 5663 |
rs562664224 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186106 | TTCAAATGTTGGCTA[C/G]GTGCGGTGGCAACCT | 5663 |
rs562686985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73153352 | AGGCTTAAGCCTAAC[A/G]TAACAGCCCCATAAG | 5663 |
rs562710736 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152533 | AATTGCTTGAACCCA[C/G]GACTCAGAGGTTGCA | 5663 |
rs562733261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205351 | AGGCATGGTGGCGGG[C/T]GCCTGTAGTCCCAGC | 5663 |
rs562889925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73138611 | TCCCGCCTTGGCCTC[C/T]CAGAGTGGTGGGATA | 5663 |
rs562909101 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73204426 | TTAACAAATATACTA[C/T]TTATGATAATTAACA | 5663 |
rs562924906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139252 | CGCGCCACTGCACTC[C/T]AGCCTGGGCAACAGA | 5663 |
rs562945570 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73205690 | GATGTTACCAAATTT[C/T]CCTCCAGTGGGGATT | 5663 |
rs563018986 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196472 | CCACTTTGAGGCATG[A/C]AATTTTTTTTTTTTT | 5663 |
rs563021515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73176227 | CAAAAAGCAAGTGAT[A/G]TAAACCCATGCTGGG | 5663 |
rs563035600 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73210531 | ATTAATTATGGAGGT[A/T]AATACCAAAAGGGAT | 5663 |
rs563102078 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73215403 | AGCCTGGCCAACATG[A/G]TAAAACCTCATATCT | 5663 |
rs563166016 | in-del | -/AAAG | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73142078 | TCTCAAAAAAAAAAA[-/AAAG]AAAAGAAACTACATC | 5663 |
rs563199097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216886 | TTATTACTTATTATT[A/G]TTATTGATAAATAAC | 5663 |
rs563211565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73161182 | GTTTCACCATGTTGC[C/T]CAGGCTGGCCTTGAA | 5663 |
rs563262762 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73184929 | TCACCTCCCAGACGG[C/G]GTCGCGGCCGGGCAG | 5663 |
rs563263950 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73180183 | AGAGATGAGGGTTCC[C/G]CATGTTGCCCAGGCT | 5663 |
rs563304655 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73174886 | TAGCTCGCTCTTTTG[C/T]CAAAGTGACCTACTG | 5663 |
rs563327348 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134691 | CACCACGCCTGGCTA[A/T]CTTTTTTTGTATTTT | 5663 |
rs563330043 | snp | A/C | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217752 | CCCACATAGATCTTG[A/C]TGATAGTGCTACAGC | 5663 |
rs563422732 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73189388 | GGCCGAGGCGGGTGG[A/T]TCACCTGAGGTTAGG | 5663 |
rs563459557 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73180859 | AACATATTTGACATA[C/T]TGACTTTGTCAAGAT | 5663 |
rs563472748 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179324 | CGAGAATGGAGAAAA[G/T]CGGAAAAGAATGCCG | 5663 |
rs563474000 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73181595 | AGACCCCAGTCTCTT[-/A]AAAAAAAAATCATAT | 5663 |
rs563525383 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210065 | AAATCACTGTGTTAA[C/T]GGAACTAGAAGTTAC | 5663 |
rs563558461 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136377 | CCGGAGGCCCCGCCC[C/T]CTTCCTCCTGGCTCC | 5663 |
rs563573153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73172099 | GTTAATTGAAAGGAT[A/G]AACAACTAATTCAAG | 5663 |
rs563574480 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73191406 | ATGTATAAGTGTGTG[C/T]GTGTGTATGATGATT | 5663 |
rs563660334 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73145646 | AGCCCGGCCTCATGC[A/G]ATTTATTGACTACTT | 5663 |
rs563710386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151557 | ACAGTTATTTAATAA[C/T]TTAAAAAGCTATTTT | 5663 |
rs563734399 | in-del | -/TTTGTTTG | 0.0263992 | 0.111815 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201075 | AAAAGAGAATATCTT[-/TTTGTTTG]TTTGTTTGTTTGTTT | 5663 |
rs563749233 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73144319 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGCC | 5663 |
rs563773430 | in-del | -/ACAG | 0.00159617 | 0.0282053 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221156 | TTATATTAGGCAGTC[-/ACAG]ACAGGAAAAATAAGA | 5663 |
rs563912898 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197502 | AAGTACTTCTCAGTA[G/T]TACGTAATACTGCTT | 5663 |
rs563953471 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73147545 | TTCCTTAAGATTACT[C/T]AGCTCCCTTTGCTGG | 5663 |
rs563956596 | in-del | -/AG | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162641 | CTGCAGCCTAGTGAC[-/AG]AGAATCTGTCTCAAA | 5663 |
rs563989315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206950 | AATAACTGAAATATG[A/G]TTTGAGATGTGCTGA | 5663 |
rs563992088 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73140044 | CTCAGAATTTTAGAC[A/C]ATGATTTTGAATAAT | 5663 |
rs564069007 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154266 | CTGTTTTCTTTATAA[A/G]ATTACCTAAATTCAT | 5663 |
rs564097663 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212879 | GGTTGTCTTGTTTTT[G/T]CAAGAGTGAAACTTG | 5663 |
rs564123399 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73139450 | GCCGGGTGTGTTGGC[A/G]TGTACCTGTTATCCC | 5663 |
rs564218908 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73207747 | ACTCAGCCTAGCTGG[A/C]TATGCTTGGCTTTCT | 5663 |
rs564268652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73170067 | GGACGTTGCCATGGC[A/G]TCTGTAAACTGTCAT | 5663 |
rs564281625 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154671 | TAGGACAAAGGCTTG[A/C]AATATATGACAGATA | 5663 |
rs564306044 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73199469 | CAGCACATGAAATGG[C/G]TGCATAGTGTTCTCT | 5663 |
rs564310984 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193654 | TTTATATCTTACTGC[A/G]GAAGCTTTTTTCTTT | 5663 |
rs564321511 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200995 | GGCGGAGGTTACAGT[C/G]AGCCATGATCGTGCC | 5663 |
rs564331549 | snp | G/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223087 | TAGTGCGTTGTGAAA[G/T]GGCTGGCCAGAGTGT | 5663 |
rs564404577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201635 | AGAGGTATAGTAAAT[A/G]TCATGTACTACATCA | 5663 |
rs564440047 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73202366 | TAAACATGTATGTTA[A/C]TTTAATACTCAGAAA | 5663 |
rs564490926 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221922 | AGTAGAGTATGACCA[C/G]CCAAGCCAATCTGCT | 5663 |
rs564555126 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73157920 | GAACCCAGGAGGCAG[A/C]GGTTGCAGTGAGCTG | 5663 |
rs564591921 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168646 | TTCCCATACCATCCC[-/T]TTTTTCAACTCCCCA | 5663 |
rs564592962 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179148 | TTCCTAAAGTCAGGG[C/G]CAAAATGTGGGAGGA | 5663 |
rs564626869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73172737 | TAATGCACATACTTT[C/T]TCTCTCATAGAGTAG | 5663 |
rs564677663 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73163800 | GAGAGGAGGAACAGT[C/T]TGTGGTCAGAGCAAG | 5663 |
rs564729161 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216193 | AATAGGCGAGGCATG[G/T]ATTGTATGAGTCATA | 5663 |
rs564743486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73167530 | ACCCAGTCACCTCCT[A/G]AAGGCCTCACCTCTT | 5663 |
rs564840699 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194433 | AATTTTTTAAAAAAA[A/C]ATTTTTTTTCAGAGA | 5663 |
rs564842245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156263 | TGGGAGGCTGAGGTC[A/G]GAGGATGACTTGAGC | 5663 |
rs564845554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205251 | GGAGGCTGAGGCGGG[C/T]GGATCACGAGGTCAG | 5663 |
rs564885012 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136361 | CAATCGTTTCTCCAG[A/G]CCGGAGGCCCCGCCC | 5663 |
rs564987355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198433 | ATTCCTTTGAGTGAC[C/T]GGTTTAGATGTCTTT | 5663 |
rs565006875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212184 | GGTGCGATCTTGGCT[C/T]ACTGCAAGCTCCACC | 5663 |
rs565033937 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210227 | AATATAAAATTCATC[A/C]GTGGAAAAAAATGAG | 5663 |
rs565086696 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PSEN1 | GRCh38.p7 | 14:73218653 | CTCCCACACAGCATA[A/G]AGAATGCTCCCGCAC | 5663 |
rs565216273 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151830 | TGTCTTGGCCTCCCA[A/G]AGTGCTGGGATTACA | 5663 |
rs565259238 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192987 | CATAACTCTTCAGTA[A/T]ATCATTAATTAGCTA | 5663 |
rs565288158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73185024 | GCGGCCGGGCAGAGA[C/T]GCTCCTCACTTCCTA | 5663 |
rs565338924 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152034 | CTCCTGCCTCAGCCT[C/T]CCAAGTAGCTGGGAC | 5663 |
rs565341355 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73208673 | GGGAGGAAGTACATG[A/C]TGATGGGTCCATGGG | 5663 |
rs565393164 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | PSEN1 | GRCh38.p7 | 14:73183304 | TGTATTTTTTTTTTT[A/T]AATTTATTTTTTATT | 5663 |
rs565456669 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73217533 | TTCTGTTTAGGAACC[A/G]CTGCCTCAAGCCTAG | 5663 |
rs565502483 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73214130 | GTATATTCATACAAT[G/T]GAATATTACTTGGTT | 5663 |
rs565579294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186464 | TTGCCAAATTGTACT[A/G]TTTTATAAAGTTGTT | 5663 |
rs565674846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73202574 | ACCTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC | 5663 |
rs565681598 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73170739 | ATCCCAGGTCTAACC[G/T]TTACCTTGATTCTGC | 5663 |
rs565745883 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187100 | GAGACATTCTTCTGT[G/T]GCTCCTTGCTTATAA | 5663 |
rs565751266 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73215143 | TTTTTATATTTTTAG[A/T]AGAGACAAGGTTTCA | 5663 |
rs565758357 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73140336 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 5663 |
rs565795309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73178704 | ATTCCTATATAGCCC[A/G]TCTTTACATTTTTTT | 5663 |
rs565824536 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162449 | CGCTCGCTCGCGCGC[G/T]CTCTCTCTCTCTCTC | 5663 |
rs565888917 | in-del | -/C | 0.00159617 | 0.0282053 | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73223937 | AGCAAGACTCTGTCT[-/C]AAAAAAAAAAAAGTT | 5663 |
rs565926375 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73215862 | TGGAAATTCAGACTG[C/G]TACAGCCAGTGTGGA | 5663 |
rs565942079 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156590 | ATAATTATTGAAGTT[G/T]AATAAATTGCACATG | 5663 |
rs565972477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73170409 | AAGTCTTATTAATTA[A/G]GGTAAGATAGTTCCT | 5663 |
rs565976568 | in-del | -/TA | 0.00438332 | 0.0466095 | intron-variant | PSEN1 | GRCh38.p7 | 14:73190540 | TGTCAAGTAGAAAAG[-/TA]TATATATATGACATG | 5663 |
rs565996594 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162974 | TATTTATTTATTTTT[A/C]ATTTTTGCTTTGCCT | 5663 |
rs566008136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73180513 | CCCTGAGGATTTTTC[A/G]TATCAGTGGTTGGTT | 5663 |
rs566015579 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195293 | TTCTCCTGCCTCAGC[A/C]TTCCGAGTAGCTGGG | 5663 |
rs566019935 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73173203 | TCTGACAACCACTTG[G/T]CAGCCCACGTGGTTT | 5663 |
rs566047498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181089 | GATTCCATGCATAAG[A/G]CAAAGGTTCAATTGT | 5663 |
rs566077284 | snp | A/G | 0.0109552 | 0.0731956 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208858 | TGCCATCAACCTGCT[A/G]TCTATAGCTCCCATG | 5663 |
rs566113957 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73209387 | TGGAAAGAATTGCCA[A/C]AAGCCTGGCTCTTGT | 5663 |
rs566115873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201958 | CGCCACATTGGCCAG[A/G]CTGGCCTTGAACTCC | 5663 |
rs566176713 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195877 | TATCCCTGTTTTACT[G/T]CTAAGAAACTTGAAG | 5663 |
rs566194421 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135676 | CCCGGCCGCTTGGGG[A/G]TGGATTTTTAAAGAA | 5663 |
rs566296887 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73193155 | TATCTACAGAAAATA[C/G]AAAAATTAGCCGGGC | 5663 |
rs566301886 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73188884 | ACTTCTGCCTCCTGG[G/T]TTCAAGCGATTCTCC | 5663 |
rs566406990 | snp | C/T | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134557 | TTTGAGACATAGTTT[C/T]GCTCTTGTTGCCCAG | 5663 |
rs566408509 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PSEN1 | GRCh38.p7 | 14:73184079 | CACCTCCCTCCCAGA[C/T]GGGGCGGCTGGCCGG | 5663 |
rs566447360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73185461 | CCAGTCAGGCGTGGC[A/G]GCGTGAGTCTGCAAT | 5663 |
rs566456126 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194255 | TTTTTTTTTTCTTTT[A/T]GTTTTTTTCTTCCAA | 5663 |
rs566481953 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73176437 | AGGGTGGAATTCTAC[A/T]TTTTCTTTCTTATAA | 5663 |
rs566510310 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205082 | CTTTGATTGTGTGTT[G/T]CTTTCATAAGTTCTT | 5663 |
rs566520853 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145227 | CTTGCATTACCCTTT[A/C]TTTGCCTTGTTTCAT | 5663 |
rs566542756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205396 | AGGCAGGAGAATGGC[A/G]TGAACCCAGGAGACG | 5663 |
rs566558589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73159724 | AACTGAAACTCTATA[C/T]TCATTGGACAACTTT | 5663 |
rs566596264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192535 | GTTATGGTAAAATTA[C/T]AAAGGTGGGATATTA | 5663 |
rs566600750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73144856 | TGCTCATATTTAACC[C/T]ATAAGCATAATATAG | 5663 |
rs566742120 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193126 | ACCAGCCTGGGCAAC[A/G]TGGCAAAACCTCGTA | 5663 |
rs566760377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73207413 | ATCTGAAAAACAACA[A/G]GCACAGTAAATATTG | 5663 |
rs566795256 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200711 | TGTATATCCTTGTAG[A/G]TTTTTTTTGCCAATT | 5663 |
rs566808180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73138715 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGTGG | 5663 |
rs566830634 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209071 | CAGCCTCAGCCACAA[C/T]TTTGCTCTGAAATCG | 5663 |
rs566833862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201128 | GAGTCTTGCTGTGTC[A/G]CCCAGGCTGGAGTTC | 5663 |
rs566842842 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219719 | AAACTACACGTTGAA[A/T]ATCAACCCAATAATT | 5663 |
rs566845589 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168719 | ATATACTACCCTTCA[A/G]TCTGTTCATGTGATC | 5663 |
rs566914706 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221212 | TAAAGTAGTAGGTTC[C/T]ATCATCTCAATTCAT | 5663 |
rs566968209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73180429 | TTGTTTACTTTGACA[C/T]CCAGTATAACTAAAA | 5663 |
rs566979881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216370 | TTGTACAGCTCTCTC[C/T]ATATATAGTTGTACA | 5663 |
rs566984378 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168974 | CCACACTCACTCACT[C/T]GCTTGCACACTGCCT | 5663 |
rs567021449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73161540 | CATTGAAATGATATG[A/G]ATTAAATTTAGCAAC | 5663 |
rs567072770 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154365 | TACTTTGGGAGGCTG[A/G]GGCAGGAGGATCCCT | 5663 |
rs567090489 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200174 | TGTCTAATGCTTTGG[G/T]TGATTATTTGAACTT | 5663 |
rs567118609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217005 | TGAAGCCTAATTTTG[C/T]ATATCATTTACTGAC | 5663 |
rs567118665 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73209606 | CTATTTGGAGAGATA[A/G]ATGGTCAACAAATTA | 5663 |
rs567134128 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223055 | AAGAGATTAAAAACA[C/G]AGGTTTCAGCTCTTC | 5663 |
rs567154919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210199 | ATTTCAGGATAAATT[A/G]GTCATAGATAATAAT | 5663 |
rs567207657 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73208465 | TGTCTGCAGGCAGGT[C/T]ATCCTGATGTCTGTA | 5663 |
rs567210692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73147135 | GGATTACAGATGCGC[A/G]CCACCACACCCGGCT | 5663 |
rs567218734 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73156803 | GAGTAGCTGCGACTA[C/T]AGGCGTCCGCCACCA | 5663 |
rs567228074 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200188 | GGTGATTATTTGAAC[-/T]TTTTTTCATGTGTTT | 5663 |
rs567524016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73203701 | AGAAAAAATATACAC[C/T]TACTCTTTGAGCTAA | 5663 |
rs567560768 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196893 | CAGTGTTTAAAATTA[C/T]TTTTATATTTTTATA | 5663 |
rs567626419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143030 | TGTTGTTGTTTTTGT[C/T]GTTCACAGGGCTAAG | 5663 |
rs567645483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158265 | TCCAATATGGTAGGT[A/G]TATATTTAACTTTTT | 5663 |
rs567663120 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136077 | TTGATTCATTGAGTG[A/G]TGGGAGAGGGCAGAG | 5663 |
rs567725268 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73138996 | AAATGTAAAAAGAGG[C/G]TGGGTGGCCGGGCGC | 5663 |
rs567742195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181201 | TCCCAGCACTTTAGG[A/G]GGCTGAGGTGGGCGG | 5663 |
rs567780627 | in-del | -/CTAAA | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145750 | TAAAGCTGAACAGTT[-/CTAAA]CTGAACTGTCATCAG | 5663 |
rs567817615 | in-del | -/T | 0.0607341 | 0.163335 | intron-variant | PSEN1 | GRCh38.p7 | 14:73138385 | ACCACGCCCGGCTAA[-/T]TTTTTTTGTATTTTT | 5663 |
rs567820463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73218793 | CTGGGTTTTTAACCA[G/T]CCAAACTAAAATCAC | 5663 |
rs567855571 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73174085 | TATTATGATTAGTTA[C/T]CAAGATTTAGTGATA | 5663 |
rs567868905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73218162 | AGTGACATTAGCTCA[C/T]TGCAACTTCTGCCTC | 5663 |
rs567918923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210992 | AAGACATTCACTCCC[C/T]GCTCCTTTCCCAATC | 5663 |
rs567933217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73146248 | GGCTGAGTACAGTGA[C/T]GAGATCTTGGCTCAC | 5663 |
rs567940282 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73165831 | GTGAGGCCAAGGTGG[A/G]CGGATCATGAGGTCA | 5663 |
rs568059744 | snp | G/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222640 | TGAGGATGCAAAGAT[G/T]AATAAGATAAATTCT | 5663 |
rs568074659 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73197488 | TGCCCTCTTACTTCA[A/G]GTACTTCTCAGTAGT | 5663 |
rs568093198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193288 | GTATTCCAGCCTGGG[C/T]GATAGAACAAGACCT | 5663 |
rs568129871 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193787 | TCAGCCTCTCAAGTA[G/T]CTAGAACTACAGGTG | 5663 |
rs568131652 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73185613 | AGGGAGACCGTGGGG[A/G]GAGAGAGGGAGAGGG | 5663 |
rs568168329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186320 | GGAGGCGGAGGTTGC[A/G]GTGAGCCGAGATTGC | 5663 |
rs568181348 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143121 | AGTGGGGTCATTGAC[C/T]GCCATGCAATCCTCA | 5663 |
rs568194142 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139449 | AGCCGGGTGTGTTGG[C/G]GTGTACCTGTTATCC | 5663 |
rs568214900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73155073 | TCTGAAAGTTTATCC[C/T]ATAAAAATATTACCA | 5663 |
rs568227981 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141651 | TTAGCTGGGCATGGT[C/G/T]GTGGGCGTCTGTAAT | 5663 |
rs568230975 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73182079 | GTGCCTGGCCTGAAA[A/G]GGAAATGTTGGTATT | 5663 |
rs568248682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169268 | TATTCTCTTAATCTC[A/G]TTTTCTGGTTTTCTC | 5663 |
rs568251929 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73155932 | AATGTAGGTTCATCT[C/G]TTGTAACGGTTTACC | 5663 |
rs568262304 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73191829 | CTGGGATTAGAGTGT[C/G]AGCCACTGTGCCTAG | 5663 |
rs568318853 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73214057 | TAATATTGTTCATAA[A/C]AGGTAAAAACAGAAA | 5663 |
rs568329384 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73178674 | GTTTTTGGTTATTTT[A/T]TTTTTAGTTCTAAAA | 5663 |
rs568351546 | snp | A/G | | | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73138018 | AGGAGGTTGCAGTAA[A/G]CCAAGATTATGCCAC | 5663 |
rs568363633 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169760 | AGGTGATTCTCCTGC[C/T]GTAGCCTCATGAGTA | 5663 |
rs568382889 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73164160 | AAGGAAAAGAATCAA[G/T]AATAATTCCTAGATT | 5663 |
rs568420160 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73188654 | AAAATAAATAAATAA[A/C]TAAATCTCTAACATT | 5663 |
rs568432296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179469 | TAAAATACAAAAAAT[C/T]AGCCAGGCATGGTGG | 5663 |
rs568455702 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73179991 | CCTTCATTTTATTTT[A/T]TTTTTTTTTTTGAGA | 5663 |
rs568460425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73214941 | TGTTAAACTTGATGG[A/G]TATCTTACCACAGTT | 5663 |
rs568469551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194633 | GAGTGCAGTGGCGTG[A/G]TCTTGGCTCACTGCA | 5663 |
rs568497767 | snp | A/G | 5.14637e-05 | 0.0050724 | missense | PSEN1 | GRCh38.p7 | 14:73148087 | AGGACAACCACCTGA[A/G]CAATACTGTACGTAG | 5663 |
rs568532621 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73140761 | GGGATTCTGGACTTG[C/G/T]GATTCTAAGTCTTTG | 5663 |
rs568547787 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201756 | TTATTTTATTTATTT[A/T]TTTTTTTTGAAACAG | 5663 |
rs568619097 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73138739 | GCCGTGGCGGGCGGA[G/T]CATGAGGTCAGGAGA | 5663 |
rs568681560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195233 | GCTGGAGTGCAGTGG[C/T]GTGATCTCAGCTCAC | 5663 |
rs568720978 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73213846 | GATAGACAATAACAG[A/G]TGTTGGTGAGGATGC | 5663 |
rs568722981 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73188405 | ATGTTTATAATCTCA[A/G]TACTCTGGGAGGCTA | 5663 |
rs568741200 | snp | C/G | 1.83731e-05 | 0.00303087 | missense | PSEN1 | GRCh38.p7 | 14:73198036 | CTTTTTCTAGATTTA[C/G]TGGCTGTTTTGTGTC | 5663 |
rs568814612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211676 | AAGGGCCAGCTAGTT[A/G]CAATGACAGCTAGTT | 5663 |
rs568887817 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204528 | AATGCTTTTTACATT[A/T]AAAAAAAAAAAAAAA | 5663 |
rs568930445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151974 | TGGAGTGCAGTGGCA[C/T]GATCTCGGCTCACTG | 5663 |
rs568952237 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204981 | GTATTGCCTGCCTGG[A/T]TTCTGTTAACTTTTG | 5663 |
rs568966020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151388 | TATGGATCTTAGAAC[C/T]ATTTTAGAGATTGCT | 5663 |
rs569005122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143767 | CCTGTAATCCTGGCT[A/G]GTTGGGAGACTGAAG | 5663 |
rs569037477 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73154959 | AAGTTAGTATTTATT[G/T]GGAGGCAAGCTCTTA | 5663 |
rs569141866 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73182516 | AATAATTAAAAAAAA[A/T]ATATTTGGGGGCTCC | 5663 |
rs569218791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73137007 | GAGCATTCTGGGCGA[A/G]GTCCGCACGCCTCTT | 5663 |
rs569235299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73175379 | TGATCCACCCACCTC[A/G]GCCTCGCAAGGGCTG | 5663 |
rs569258375 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73138026 | GCAGTAAGCCAAGAT[C/T]ATGCCACTGCACTGC | 5663 |
rs569280213 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73174416 | TTTTTGTATTTTTAG[A/T]AGAGACAGGGTTTCA | 5663 |
rs569321656 | in-del | -/CTC | 0.00557542 | 0.0525036 | intron-variant | PSEN1 | GRCh38.p7 | 14:73182885 | AATAAATAAGAACAT[-/CTC]CTTCTTCCTTTGCCA | 5663 |
rs569393568 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168230 | GCATGGTGGTGGGCA[C/T]CATAATCCCAGCTAC | 5663 |
rs569418473 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73183492 | AGATTAGGGAGTGGT[A/G]ATGACTCTTAACGAG | 5663 |
rs569431165 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160021 | TAGAGACGAGTTCTC[G/T]CCATATTGGCCAGGC | 5663 |
rs569450712 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222990 | AATCATAAGTTTGAG[C/T]CTAGAAGTGATCCTT | 5663 |
rs569467597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205619 | TGTATCTTCAGGATA[A/G]GTTCCAAAATGTAAT | 5663 |
rs569482154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73153799 | CTCACTGCAGCCTCT[A/G]CCTCCCAGGTTCAAG | 5663 |
rs569493344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73215975 | GAAATGAAAACAGTC[C/T]GTCCCCACAGAGACA | 5663 |
rs569533437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152861 | CAGCCTGGCCATCAC[A/G]GTGAAACCCTGTCTC | 5663 |
rs569571306 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160644 | TTAGTGATGTTGAGC[A/T]TCTTTTCTTTTTTCC | 5663 |
rs569579430 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73163672 | TAGTCAGGAAATTCT[C/T]TCTCTACCAGGAGGG | 5663 |
rs569597522 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73178836 | CAATTGATCTGATTG[C/G]GCTAGGTCCAGCCAG | 5663 |
rs569601680 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73195647 | CCCAGGCTGGAGTGA[A/T]GTGGCACGATTATAG | 5663 |
rs569649989 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141487 | AAATTAGTTTAAAAA[A/T]TTTTTTTATTAATTT | 5663 |
rs569682048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187961 | TTTTTTTGAGTCTCA[C/T]GCTGTTGCCCAGGCT | 5663 |
rs569722047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73142120 | AATAATAATTTCAAT[C/T]ATAGGTTGGAATTTA | 5663 |
rs569769165 | snp | C/T | 0.000362253 | 0.0134535 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208914 | GTGCCTGCAGGCCCA[C/T]GGTAAGCTGCCTTCA | 5663 |
rs569857101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73142938 | ACCAGAGAGCAAAAA[C/T]ACCAGAGTAGATTCT | 5663 |
rs569858965 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135036 | AACTATTGTATGTAT[C/T]AGGCACTGTTATGTA | 5663 |
rs569867055 | snp | G/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223201 | CCTCAGATTTGCATA[G/T]AAAAAAGCACCCTGG | 5663 |
rs569886286 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73209519 | AGATGTTGACTGAGC[A/T]CCTGACTATGTGCTA | 5663 |
rs570130617 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196767 | AGCATAAGCCACTGT[A/G]CCTGGCAAGACATGA | 5663 |
rs570172362 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73189687 | ATAATAAAAGGATAA[G/T]TCCCATTTATGATAG | 5663 |
rs570238489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181703 | CACTAGTTGATTCTC[A/G]CTGTTAAGGTCTTTA | 5663 |
rs570255516 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73146122 | AAATAAAGACAGGAA[A/C]AAAGGTATCGATAAC | 5663 |
rs570278810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181165 | ATAGTTTCAGCTGGG[C/T]GTGGTGGCTCACGCA | 5663 |
rs570290867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73138859 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 5663 |
rs570393716 | snp | A/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221609 | TTTTTTTTTTAAAGG[A/T]CAGGATTTTGCTGTG | 5663 |
rs570400503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73176611 | TAAAAGAGAAAACAC[C/T]ATTTCTAAACTACCT | 5663 |
rs570404012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217300 | TCAAAACTTTGATTA[C/T]ACAGTCCCTTTAAGG | 5663 |
rs570447127 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73188709 | AAGGCCAATGTCATC[C/T]TCATAGGGAAGCTAG | 5663 |
rs570454514 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206159 | ATGAAGAGTTTTGTG[A/G]TAGCAGGTGCAGTTT | 5663 |
rs570457259 | snp | C/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223575 | TGTACTTAATTCAGA[C/G]AGACTGTGAATACAC | 5663 |
rs570474027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169099 | GACTTCCCTCTTCAC[C/T]GTTTTACTTTTGTAA | 5663 |
rs570560360 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167173 | TGATTATGCCATGGT[A/G]GATAGACAGAACGGC | 5663 |
rs570563162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193194 | GCACACCTGTAGTTC[C/T]AGCTACTTAGGAGGC | 5663 |
rs570584451 | in-del | -/AGGTCA | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193238 | TCGATTGAGCCCAGG[-/AGGTCA]AGGCTGCAGTGAGCC | 5663 |
rs570593680 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73164965 | TTGTACTTTTTTTTG[-/T]TTTTTTTTTGAGACG | 5663 |
rs570604592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73185559 | AGTACAGTCCAGCTT[C/T]GGCTCAGCATGAGAG | 5663 |
rs570623283 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204398 | TTTAAAAAAATATTA[-/TT]TTTTAGGACTATTTA | 5663 |
rs570642073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73164140 | GCTGACTAGACAGAG[A/G]TACTAAGGAAAAGAA | 5663 |
rs570749341 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73216868 | ATATTCAATAGATGA[C/T]GATTATTACTTATTA | 5663 |
rs570774605 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194499 | CTCCTGGCCTCAAGC[G/T]ATCCTCCCACCTTGG | 5663 |
rs570775798 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73146901 | ATCATAAAGAATTGG[C/T]TGATGGAAATTAAGG | 5663 |
rs570787560 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73188318 | TCTCTGTATGTGCTA[A/G]AAGGCATTTGATAAG | 5663 |
rs570804355 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73190066 | AGAGCTGCTAGTGCA[A/G]GCTGTGCAGAGGAAG | 5663 |
rs570808816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73207635 | CATGTTAGACTCTCA[C/T]GGGATCCTTAGGGTG | 5663 |
rs570834943 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221279 | CCTCTCTCAGACATG[G/T]GCTAGCATGGGTATT | 5663 |
rs570845595 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209180 | GCAGCTGTGGGAGTG[C/T]GGGACTTCTGCCCCA | 5663 |
rs570864982 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158708 | CTCAAGTGATCCTCC[A/C/T]GCCTTGGCTTCCCAA | 5663 |
rs570945059 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73160936 | CTTTTTAATGTATTC[-/T]GGATATTAATCTCTT | 5663 |
rs570991268 | snp | C/T | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154920 | GGGAAATAGGCTTTC[C/T]TGTATGCTGTGTTCT | 5663 |
rs571028225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73147924 | GTTTTTTATAACAGT[A/G]TAATTGTAGTGCACA | 5663 |
rs571068935 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187127 | ATAATAAGTAGAACT[A/G]AAAGAACTTAAGACT | 5663 |
rs571099005 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73203925 | TTGGGAGGTAGAAGC[A/C]GGAGGATTGCTTGAG | 5663 |
rs571218451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197756 | GGAAGACTTGTTCCT[A/G]TACCCCAGTAACGAT | 5663 |
rs571236187 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73217143 | GGAGTAAAACTTGGA[C/T]TGGGAGATTTCATTT | 5663 |
rs571279658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73165562 | ACCAGCCTGACCAAC[A/G]TGGATAAGACTCCAT | 5663 |
rs571344413 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210861 | GAAGAATAAAAGTAC[G/T]TTGAACTTCACTTAT | 5663 |
rs571434401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73150593 | ATGGTGAAACCCTGT[C/T]TCTACTAAAAAAAAA | 5663 |
rs571524399 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219604 | ATCAGCAGCTTGACG[C/T]GTGGTCACAGGACGA | 5663 |
rs571600800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73191310 | ATAAATGGGATCCTA[C/T]ATTTTTTCAAGCAAC | 5663 |
rs571652765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181794 | CGTATTTTTTTTTGA[C/G]ACAATGTCTCACTTT | 5663 |
rs571701901 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73164324 | AATTCCATAGTGCCG[A/G]CGATTTTCTATTGAT | 5663 |
rs571773400 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73172078 | TAATAAATGGCCAAA[C/T]GAATTGTTAATTGAA | 5663 |
rs571815825 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73179911 | GAGTGGAAGGTACTT[-/A]ACTCCATCTTATCTG | 5663 |
rs571825723 | snp | C/T | 0.000115313 | 0.0075923 | missense | PSEN1 | GRCh38.p7 | 14:73211867 | CATCTAGGGCCTCAT[C/T]GCTCTACACCTGAGT | 5663 |
rs571873003 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73159889 | GTGCAGTGGCATGAT[C/T]TTGGCTCATGGCAGC | 5663 |
rs571899169 | in-del | -/TTGTTT | 0.00359567 | 0.0422482 | intron-variant | PSEN1 | GRCh38.p7 | 14:73190852 | AGATTAATAAATAGA[-/TTGTTT]TTGTTTTTGTTTTTT | 5663 |
rs571900892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158858 | TCCAGTTCCTCCACA[C/T]CCTGTCAGTACTTGA | 5663 |
rs571993003 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73202294 | GAGTCCGTGGCAAAA[A/G]TGTGAGTACAGAGAT | 5663 |
rs572002708 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154596 | GCAAAGTGAGACCCT[C/G]CCTCAAAAAAAGAAA | 5663 |
rs572022100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168890 | TGGATGCTGCTGCGG[A/G]GCCGCATAGAGCCTG | 5663 |
rs572033004 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73139310 | AGGCTGGGCACAGTG[A/G]CTCACACCTGTAATC | 5663 |
rs572034792 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73168767 | TGGAAGAGAACCTGG[G/T]TGCCAAGAGGAGAGG | 5663 |
rs572073455 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73141797 | TCTTGGCCGGGTGCC[A/G]TGGCTCACGCCTGTA | 5663 |
rs572085113 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | PSEN1 | GRCh38.p7 | 14:73213411 | TTCGTCTCCAACTTT[A/T]AAAAAAAAAAAAGTG | 5663 |
rs572119311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169374 | CACAGCTATTTCATC[C/T]ATTTCTGAGGCCTGA | 5663 |
rs572121460 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73174218 | AATAGCACAATCTAA[G/T]TGGGTTTTTGTTTGT | 5663 |
rs572145921 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221647 | GGCTAGACTTGAACT[C/G]CTGGGCTCAAGTAAT | 5663 |
rs572149208 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73177754 | TCGAATCACTGTTCT[G/T]CTAAAAGTAATACAT | 5663 |
rs572182689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73214245 | ACTAAAAGACCAACT[A/G]TTGCTGGGCGCAGTG | 5663 |
rs572198095 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73165716 | TCGCACCATTGCACT[C/T]CAGCCTGGGCAACAA | 5663 |
rs572275227 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73155181 | ATTGCTTATGGTTTA[C/G]CCAGTTAGTAGTGTA | 5663 |
rs572284686 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73207704 | CTTTTCCTGAGATTT[C/G]CTCAGGCCCACTGGG | 5663 |
rs572329394 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208223 | AAGTGGGGGGCACGT[G/T]TCAGCCCTGTTTGTC | 5663 |
rs572337768 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194021 | ATGTATAGAATTATT[C/T]TTTTAAAAATAAAAC | 5663 |
rs572343288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179602 | AGCCTGAGCTACAGT[A/G]CGAGACTCTGTCTCC | 5663 |
rs572343601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73170052 | TACAAGGTAACTTCC[A/G]GACGTTGCCATGGCA | 5663 |
rs572439776 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194658 | ACTGCAAGCTTCGCC[G/T]CCCAGGTTCATGCCG | 5663 |
rs572448841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187998 | CAGTGGCATGATCTC[A/G]GCTCACTGCAACCCC | 5663 |
rs572470222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201276 | TATTTTTAGTAGCAA[C/T]GGGGTTTCACCATGT | 5663 |
rs572503215 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73217538 | TTTAGGAACCGCTGC[C/G]TCAAGCCTAGCAGCA | 5663 |
rs572666729 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73159982 | TGCACTCTATCATGC[C/G]TCGCTAATTTTTTAA | 5663 |
rs572712899 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73163349 | TCGGGAGGCCAAGGC[A/C]GGAGGATTGCTTGAG | 5663 |
rs572716851 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73215641 | GATATATAAAGGATG[A/C]TTACAACTTAATACG | 5663 |
rs572734554 | snp | G/T | 3.6404e-05 | 0.00426623 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206483 | AGAAAGTAGGTAACT[G/T]TTATTAGATAATATC | 5663 |
rs572751839 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209963 | TAAATGCCAATAATG[C/G]CTTTAAGGCTTTGCA | 5663 |
rs572770137 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73189254 | TTGTTTTAGAACTAA[A/C]TGAAAACCAATTCAA | 5663 |
rs572786054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197296 | TCGAAAGAAATGGTG[A/G]TATAAACAGGAATAA | 5663 |
rs572798051 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136325 | GTGGGGAAGGCCAGG[C/T]GGAGCTCTGGGTTCT | 5663 |
rs572822828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73190321 | GGTTGAAACTCCATC[C/T]CTACAAAAAATACAA | 5663 |
rs572830535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73189247 | GTTTACTTTGTTTTA[A/G]AACTAACTGAAAACC | 5663 |
rs572888932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136614 | TCCGGGCAAGCCAGG[A/G]AGGCACCGCGGACAT | 5663 |
rs572924331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212601 | GATACAACCTTGTAC[A/G]TTATTATTCCTTTTG | 5663 |
rs573045170 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73212427 | CTTCAGACTTTTTAA[A/G]TTGGCATTTTACAGC | 5663 |
rs573181284 | in-del | -/GGGCGGATCCTT | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137853 | CTTTGGGAGGCCGCG[-/GGGCGGATCCTT]GAGCTGAGGAGTTCG | 5663 |
rs573250391 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198396 | AACCTGTTAGGAGTT[C/G]TTGATTAGGGCAAGC | 5663 |
rs573325637 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208500 | TCAGTGGAGAGGAGA[A/C]CCGGAATGGGTATCT | 5663 |
rs573325852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216076 | CTGGTAAATGGATAA[A/G]CAAACCATATAATGG | 5663 |
rs573357205 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73199200 | AGAAATGAAATACTA[C/G]AGCTTGGGAAAAAGT | 5663 |
rs573358981 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73152246 | AGGAATATCTCTGGA[A/C]AGGGATCAAGCATTC | 5663 |
rs573362065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152336 | CCAAAAAAGGCCAGG[C/T]ATGGTGGCTCACACA | 5663 |
rs573456804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193340 | TTTCAAGCTTTTTGA[A/G]GTTTTGACAAGCTGG | 5663 |
rs573542085 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73184747 | CTGGCGGGGGGCTGA[C/G]CCCCCCCACCTCCCT | 5663 |
rs573614525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201386 | CCACCGCGCCTGGCC[A/G]AGAATATCATTTTTT | 5663 |
rs573769917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73155496 | GCATAGAATCAAATA[C/T]ATATTATCATTATTA | 5663 |
rs573778278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73202105 | GCTGGAGTGCAGTGG[C/T]GCAATCTCAGCTCAC | 5663 |
rs573808461 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156177 | CCATCTCTATGAAAT[A/T]AAAAAAAAAGTAAAT | 5663 |
rs573862587 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73161382 | TGTCTATTTTTGTTT[C/T]TGTTCTTTAATTTCT | 5663 |
rs573869351 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73171947 | TCATAGCAACTTGTC[A/C]TTTCTCACTTGTCAC | 5663 |
rs573888348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73142224 | CATTAGAAGTTGGGC[C/T]GCCTGTCCAGGGAGA | 5663 |
rs573926508 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135215 | ACAACTTATCTTTCA[C/T]TCTGCTAATGGAAAA | 5663 |
rs573948801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73188185 | GCCCGCCTTGGCCTC[C/T]CAAAGTGCTGGAATT | 5663 |
rs573987880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179913 | AGTGGAAGGTACTTA[C/T]TCCATCTTATCTGGA | 5663 |
rs574030149 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73169026 | TGGTGGCCGAGTAAA[C/T]GAGCCACGCTCCGAG | 5663 |
rs574067615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73138451 | GTCTCGATCTCCTGA[C/T]CTCGTGATCCGCCCG | 5663 |
rs574069889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73172432 | GTTAGGTTTGGCAAC[A/G]TATTATAGAACAAAC | 5663 |
rs574106702 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73165189 | TTGAACTCCTGACCT[C/T]GGGTGATCCGCCCGC | 5663 |
rs574123715 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73180685 | AGTTTAGGGTTTAGA[A/G]AAGATACTGTTGTGT | 5663 |
rs574138476 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217546 | CCGCTGCCTCAAGCC[A/T]AGCAGCACAGATATG | 5663 |
rs574270215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73209990 | TGCAATAATCAAAAA[C/T]TCCTCCATCCTAGTT | 5663 |
rs574271978 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223656 | TGATTGCAGATTTTC[C/T]GTATTTGTCAGATTA | 5663 |
rs574349536 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73163441 | CGAGCTTCACAAACA[A/G]TCTTACAGGAGTCAT | 5663 |
rs574374227 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160936 | CTTTTTAATGTATTC[C/T]GGATATTAATCTCTT | 5663 |
rs574386740 | snp | A/G | | | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137344 | ACTAGGAGGTTTTCA[A/G]TTTAGAACATGGCAG | 5663 |
rs574429300 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73175843 | AAATTATCTACATAT[G/T]TATAACTGTCTTGGT | 5663 |
rs574451985 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154566 | TAATCATGCCACTGC[A/C]CTTCAACCTGGGCAG | 5663 |
rs574457327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168533 | GAGAATCAGGTGAGC[A/G]TTGGAGACTATGGAT | 5663 |
rs574525529 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193415 | CTGGGTGTGGTGGCG[G/T]ACCCTTGTATTCCCA | 5663 |
rs574528005 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73184670 | CACCTCCCTCCCGGA[C/T]GGAGCGGCTGGCGGG | 5663 |
rs574566198 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73179078 | CTTTCTGTGATCTCC[A/G]TGTGGTTTCTTGGGC | 5663 |
rs574596967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186633 | AATACAAAAATTAGC[C/T]TAGCGTGGTGGCGCG | 5663 |
rs574602588 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206715 | ACAGAATACCAGCAT[A/G]GAAAGGTTCAGGCTG | 5663 |
rs574617831 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73193760 | CTCCCTGGCTCATGC[A/G]ATCCTCCCACTTCAG | 5663 |
rs574666941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212759 | CTTAGGAACATTATC[A/G]GCCACTAAAGCCCTT | 5663 |
rs574671310 | snp | A/C | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73220704 | GCTTTGTGGTCTCTG[A/C]CCGCGTTACCTTTCC | 5663 |
rs574703741 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73213369 | ACGATTCCCTCTCCT[C/G]AGAGGGCTCTTTGTG | 5663 |
rs574837074 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139282 | AGTGAGACTTCGTTT[G/T]TTTTTTAAAAAAAGG | 5663 |
rs574881861 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73159549 | CATTTTTCTGCATAT[G/T]GATATTCAATTGTTT | 5663 |
rs574926076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196504 | TTTTTTTTTTTGAGG[C/T]ACGGTCTTACTTTGT | 5663 |
rs574941431 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221818 | CATGAAAAATAGATT[G/T]TCACTGGAAAGAACA | 5663 |
rs574950495 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197032 | CCGCTTCCCGGGTTC[A/G]CGCCGTTCTCCTGCC | 5663 |
rs574976324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73178243 | TTTTTTTTTTGAGAC[C/G]GAGTCTCGCTTTGTC | 5663 |
rs575002423 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167661 | TTTAATCCCCACTTT[G/T]TCTCTTCCTCTAATC | 5663 |
rs575016434 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73145342 | TTTATTATTTTATTA[C/T]TTGTTTTTTTGAGAC | 5663 |
rs575046416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73213152 | TTCACACTCCTGGAA[A/G]AGTAGACGTATCTGC | 5663 |
rs575070944 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73186775 | AAGTGAGACCCTGTC[C/T]CAAAAAAGAAAAAAA | 5663 |
rs575111367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210283 | TTGCTCAAAAAAGCA[A/G]ATGTAATTATAGTAT | 5663 |
rs575122322 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222608 | GTGTTTTCTGTGTTC[C/T]CGTAGGTTCTGGAGT | 5663 |
rs575138549 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73149965 | GTTTTCCTTTTGTGG[C/G]CTGCTGTGCATAATC | 5663 |
rs575148584 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204061 | TGGAGTGCAATGGCA[C/T]GATCTCGGCTCACCA | 5663 |
rs575179549 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73208220 | GGCAAGTGGGGGGCA[C/T]GTTTCAGCCCTGTTT | 5663 |
rs575188803 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73181890 | GCAATCCTCCCACCT[C/T]AACCTCCATGGTAGC | 5663 |
rs575190108 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209338 | GCTGCCATCAAGACC[A/G]CTAGTAAACCTGATA | 5663 |
rs575244414 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73150627 | AAAATTTAGCCAGGC[A/G]TGATGGCAGGCACCT | 5663 |
rs575408589 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73142433 | AAGCCCTTTGTGCTA[G/T]AGATCATGGTTAAAA | 5663 |
rs575428437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181409 | GCCATTGCCCTCCAG[C/T]CTGGGCAACAAGAGC | 5663 |
rs575482072 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136222 | GAAGCACACGCTGGG[C/T]CCAATTTATATAGGG | 5663 |
rs575568437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137621 | TGGAAGAAGAGCAAG[A/G]AGCCAGCTGAGGAGA | 5663 |
rs575605579 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73177630 | ACCTTTATTACTGAA[G/T]GATATTGTTACTGGG | 5663 |
rs575633921 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222393 | TTACTTGTTATTTAC[A/G]TGGCCTCAGACAGTG | 5663 |
rs575652870 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204769 | AGGCTGGGTGCAGTG[G/T]CTCATGCCTGTAATC | 5663 |
rs575677810 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73199345 | TTTGTCAACTACTGT[A/G]TTTAGAGAATGAGAC | 5663 |
rs575717623 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151640 | AACTCACTGCAACCT[C/T]GACCTCCTTGAGACC | 5663 |
rs575745672 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205201 | CTGTGACCAGGCCGG[A/G]CGTGGTGGCTCACGC | 5663 |
rs575754374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73166036 | TAGGCGACAGAATGA[A/G]ACTCTGTCTCCAAAA | 5663 |
rs575779932 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198280 | TCTTTGTTTCCTTGC[A/G]AGCAATTGTCTTCTA | 5663 |
rs575795137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158334 | TCTATCTATCTATCT[A/G]TTTTTAAGACGGAGT | 5663 |
rs575801257 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73156233 | TGGTGGCATGTGCCT[A/T]TAGTCCCAGGTACTT | 5663 |
rs575813631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201992 | CCTCAAGTGATCCAC[C/T]TGCCTCGGCCTCCCA | 5663 |
rs575844523 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73203359 | TCCCAAAGTGCTGGG[A/T]TTACAGGCATGAGCC | 5663 |
rs575845029 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145022 | CTCAGCCTCCTTAGT[A/T]GCTGGGATTACAGGC | 5663 |
rs575908720 | in-del | -/TCTATCTATCTA | 0.0248432 | 0.108648 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158283 | TATTTAACTTTTTTT[-/TCTATCTATCTA]TCTATCTATCTATCT | 5663 |
rs575930008 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145503 | CCCACACCCAGCCAA[A/T]TTTTTTTGTATTTTT | 5663 |
rs575947856 | in-del | -/A | 0.0123036 | 0.0774623 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186783 | CCTGTCTCAAAAAAG[-/A]AAAAAAAAAATCTGT | 5663 |
rs575952097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73214280 | AAGCACCTGTAATCC[C/T]AGCACTTTGGAAGGC | 5663 |
rs576014151 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73183113 | ATGTACAGATGTTCT[C/T]AGCTTACCTTTTTTG | 5663 |
rs576074610 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145040 | TGGGATTACAGGCAC[A/G]AGCTACCATGCCCAG | 5663 |
rs576082851 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73143129 | CATTGACCGCCATGC[A/C]ATCCTCAATTGTTTT | 5663 |
rs576127513 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | PSEN1 | GRCh38.p7 | 14:73165786 | TGTGTGGCCGGGCGC[G/T]GTGGCTCACGCCTGT | 5663 |
rs576143828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73155381 | TTAAATGAGATAAAC[C/T]GAATGATTAGTACAC | 5663 |
rs576192890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169925 | TGCTGGGATTTCAGG[C/T]GCCTGGCCTGTTACT | 5663 |
rs576210394 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73202016 | CCTCCCAAAGTGCTG[C/G]GATTACAGACGTGAG | 5663 |
rs576249794 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73142022 | CAGTGAGCTGAGATT[A/G]TGCCACTGCACTCCA | 5663 |
rs576310779 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73164333 | GTGCCGACGATTTTC[A/T]ATTGATAGACTAAAA | 5663 |
rs576322359 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201333 | CCTTGTGATCCGCCC[A/G]CCTCGGCCTCCCAAA | 5663 |
rs576325374 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73217908 | ATTCTCTGCCTCAGC[C/T]TCCCGAGTAGCTGGG | 5663 |
rs576360731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194758 | TATTTGTAGTAGAGA[C/T]GGGGTTTCACCATGT | 5663 |
rs576398303 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73144954 | CTGCGGTGCAGTGGC[G/T]CAATCTTGCTTCACT | 5663 |
rs576398340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136735 | GGGCTGGGGAACCCC[A/G]TGTGGGAAACCAGGA | 5663 |
rs576433476 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73215527 | GGTGGAGGTTTCAGT[A/G]AGCCGAGATCACTTA | 5663 |
rs576434645 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137502 | TGAAAACAGGAATCA[A/T]TTCCATAGATTTCCA | 5663 |
rs576468207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73180584 | ACCTTAAAATGTTAA[A/G]AACAGGAAAGGCAGT | 5663 |
rs576496602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195320 | TGGGACTACAAGTGC[A/G]CACCACCACGCCCAG | 5663 |
rs576515346 | in-del | -/TT | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194250 | ACTCTTTTTTTTTTC[-/TT]TTTTTGTTTTTTTCT | 5663 |
rs576634775 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73209777 | CCGCTGAAGGATGGA[A/G]GAAGAGCTTTCCAAG | 5663 |
rs576671368 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186378 | GAGCGAAACTCCGTC[-/T]CAGAAAAAAAAAAAG | 5663 |
rs576694761 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73223922 | CAGCCTGGGCGACAG[A/G]GCAAGACTCTGTCTC | 5663 |
rs576713567 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73213747 | TGATCTGTAAACACA[C/T]AAAAAGATACTCAGC | 5663 |
rs576731507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216553 | ATCATGAGGTCAGGA[A/G]TTCGAGACCAGCCTG | 5663 |
rs576762765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73191162 | TTTTTTAAAAAAGAC[A/G]TTATATAAGATTATA | 5663 |
rs576790776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73191931 | GTTAGCACATGTTTA[A/G]TTTTTTCTAATTTCA | 5663 |
rs576843157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73199358 | GTGTTTAGAGAATGA[A/G]ACAAGAGAGGATACT | 5663 |
rs576860699 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73214855 | GTTCTGTGGATGGAC[A/G]ATGGTAATGGTAGCA | 5663 |
rs576871155 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73179271 | GCTTCTGCCACCCAC[A/G]TTACCATCACCACAG | 5663 |
rs576880310 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200280 | AAATTAATCTTTTTT[G/T]TGTGTGTGTGAGACA | 5663 |
rs576882779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73184534 | TGACCCCCCCACCTC[C/T]CTCTCGGACAGGGCG | 5663 |
rs576982865 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141692 | CAGGAGGCTGAGGCA[A/G]GAGAATTGCTTGAAC | 5663 |
rs576988530 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73145832 | GGAACAGGGCTGGTT[C/T]GTGGTGGCTCACACC | 5663 |
rs577050496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193872 | ATATTGCCTAGGCTG[A/G]TCTTGAACTCTTGGG | 5663 |
rs577059307 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160395 | TTTGTAATTCAGTTC[A/G]TTTTTATATATACTC | 5663 |
rs577113601 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219785 | CTGTGAGGAAGAGCA[A/G]GCACCAGCAGCAGAA | 5663 |
rs577121712 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73153171 | CTGGTTAGCCTTTGA[C/G]AGTGTTGTTGTATCA | 5663 |
rs577128548 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160704 | TTCATGTGCTTGTTG[G/T]CTATTTGTATATCTT | 5663 |
rs577161171 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204126 | GCCTCAGCCTCCCGA[A/G]TCGCCGGGATTATAG | 5663 |
rs577264909 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154050 | AATTATTGAAAAAAT[C/G]TATTTTAAGTAAATA | 5663 |
rs577269096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73203062 | GATTTTATATAAATC[A/G]TTGAGTTTGAGAGGT | 5663 |
rs577277883 | in-del | -/CCA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73156947 | GATTACAGGCATGAG[-/CCA]CCACGCCTGGCCTTT | 5663 |
rs577297639 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73197940 | CAAAAAACATTAAAC[-/T]TTTTTTCCTTCGTTA | 5663 |
rs577398268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73185972 | TGATATATGGGTGTT[C/T]ACTGTAAAATTAATT | 5663 |
rs577412933 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145759 | ACAGTTCTAAACTGA[A/T]CTGTCATCAGGGACC | 5663 |
rs577441009 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196993 | GCTGGAGTGCAGTGG[C/T]GCAATCTCGGCGCAC | 5663 |
rs577444348 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73154407 | GTTTGAGACTAGCTT[C/G]GGTAACATAGCACGA | 5663 |
rs577446560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73146595 | CTTGGTTAAAAATGT[A/G]TAATGATTTGAATGA | 5663 |
rs577518529 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139681 | TATTTCAATATCTAA[A/C]CAGTATAAAAATTTA | 5663 |
rs577543709 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216487 | GATGATAGGCCATGT[A/G]TGGTGGCTCACGTCT | 5663 |
rs577618419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195560 | ATGATCCATTTAATA[C/T]AATAATACACTTAGA | 5663 |
rs577656915 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156969 | GCCTGGCCTTTTTTT[A/T]AAAATGGTCTTACAG | 5663 |
rs577718050 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73208151 | GAGTCTGGACTCCCC[A/G]AAGGGCCACATCTCT | 5663 |
rs577771481 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135392 | TTTTTTAATTTTAAT[A/T]TTTATTTTTTGAGAT | 5663 |
rs577778596 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73149309 | AGCATGGGCAACATA[C/G]AGAGGTTCTGTGTTT | 5663 |
rs577804115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73189381 | TTTGGGAGGCCGAGG[C/T]GGGTGGTTCACCTGA | 5663 |
rs577833879 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73189975 | CCAGTTGTAGGCCAA[C/T]AACGGGGTGGAGGGG | 5663 |
rs577837150 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73209604 | GTCTATTTGGAGAGA[-/T]AGATGGTCAACAAAT | 5663 |
rs577874674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205427 | GAGCTTGCAGTGAGC[C/T]GAGATCATGCCACTG | 5663 |
rs577947701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73144190 | GGACTACAGGTGCAC[A/G]TCACCATGCCTGGCT | 5663 |
rs577975097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217736 | TGGTGCCATGCATGA[C/T]CCCACATAGATCTTG | 5663 |
rs577980368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73180802 | TTGAAATGTGTGTGT[A/G]TAACATAGTAATAAA | 5663 |
rs578030993 | in-del | -/A/AA | 0.190473 | 0.257119 | intron-variant | PSEN1 | GRCh38.p7 | 14:73215541 | GAGCCGAGATCACTT[-/A/AA]AAAAAAAAAAAGGAA | 5663 |
rs578068582 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73218267 | AATTTTTGTATTTTT[A/C]GTGGAGATGAGGTTT | 5663 |
rs578076171 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158290 | CTTTTTTTTCTATCT[A/G]TCTATCTATCTATCT | 5663 |
rs578106130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73172488 | GATCTGTCTGCTACC[C/T]TTCCACAAAGGTGTA | 5663 |
rs578187684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73203195 | GCGATTCTCCTGCCT[C/T]GGCCTCCTGAGTAGC | 5663 |
rs578218136 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152091 | TAATTTTTTGTATTT[G/T]TCATAGAGGCGGGGT | 5663 |
rs578226242 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204694 | ATACTTGCATAAAGA[A/T]AGAAAACCTAATAAA | 5663 |
rs578237909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197380 | CAGCACCACATACAT[A/G]TGTTCTGAGACCTGA | 5663 |
rs745312823 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73202285 | ACTCAAAGTGAGTCC[A/G]TGGCAAAAGTGTGAG | 5663 |
rs745315765 | in-del | -/GGATAT | 3.78294e-05 | 0.00434894 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198145 | GTAAGTATTTGAGAA[-/GGATAT]TGAATTAGTAATCAG | 5663 |
rs745393397 | in-del | -/A | 1.68883e-05 | 0.00290584 | utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73147997 | TGTTTTCTGTGAAAC[-/A]GTATTTCTATACAGT | 5663 |
rs745433204 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73190994 | GATGGTACCTGAAAC[A/T]GAAAGTTTATGCCTA | 5663 |
rs745495564 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73175513 | TTTCCAAATGTAGGA[C/G]TCTACTCTGTTTCCT | 5663 |
rs745515181 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73144710 | AGTTTAATAATGTCT[C/T]TAAGTTTTACATATA | 5663 |
rs745553779 | snp | G/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221692 | GTAGCTGAGACTACA[G/T]CCCATCTTATTTCTT | 5663 |
rs745577576 | in-del | -/ATTA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73214166 | AAGAAACAATCTATC[-/ATTA]GTACACTTAGGATGA | 5663 |
rs745579862 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222911 | CTGCCTTCCAACATT[A/G]AATTTGGAAGGAGAC | 5663 |
rs745596002 | in-del | -/AA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73199361 | TTTAGAGAATGAGAC[-/AA]GAGAGGATACTACAG | 5663 |
rs745620212 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73176982 | ACCAGTTTTTCCTTT[A/G]GTCGTATCTGCTGAC | 5663 |
rs745668592 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73202761 | ACAGGCGTGAGCCAC[C/T]GTGCCCAGCCTATCA | 5663 |
rs745688217 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73158074 | TTATGTGGTTCCTTT[A/T]TATTGCTGAGTTGTA | 5663 |
rs745694325 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | PSEN1 | GRCh38.p7 | 14:73211784 | GCACAGAAAGGGAGT[C/T]ACAAGACACTGTTGC | 5663 |
rs745710786 | in-del | -/AAA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73150765 | GTAAGACTCTGTCTC[-/AAA]AAAAAAAAAAAAAAA | 5663 |
rs745727034 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73151255 | AAATAATTCTGTTTA[C/T]AAACATTTGGTAGGT | 5663 |
rs745772998 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73198652 | TGAATTATGGTAGTG[A/G]CAGTAGCAATCAAGG | 5663 |
rs745799898 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73166102 | TAGTATCCAGCGTAC[A/T]ACAAAGAGGAAGAGT | 5663 |
rs745808202 | snp | C/T | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134807 | TGCTGGAATTACAGG[C/T]GTGAGCCACCGCACC | 5663 |
rs745845857 | snp | A/T | 0.000175269 | 0.0093597 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208840 | AGCCTGTCTGCCTCC[A/T]GCTGCCATCAACCTG | 5663 |
rs745872346 | in-del | -/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73206819 | TCCAAACATGTAAAA[-/G]TAAGAATCTCCTAAA | 5663 |
rs745891286 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73199985 | CTCCTGACTTCAGGT[A/G]ATCCGCCTGCCTAGG | 5663 |
rs745897051 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73186286 | TGGGGGGCTGAGGCA[A/G]GAGAATTGCTTGAAC | 5663 |
rs745897387 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73186998 | ATTTAAAGCCATGTA[A/C]TTTGTTGATGAATTA | 5663 |
rs745966144 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73171839 | ATTCTTTGAAATTTA[G/T]AACTCACATCTAACA | 5663 |
rs745993276 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73216842 | TAGTACAAGTGCTGG[A/G]TATAAACTATATATT | 5663 |
rs746025433 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73143821 | CAAGACCAGCCTGGG[C/T]GATACAGCAAGACCC | 5663 |
rs746032670 | snp | A/T | 1.64787e-05 | 0.00287038 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217281 | TGTGTCAGAGCTCTT[A/T]ATGTCAAAACTTTGA | 5663 |
rs746086700 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73156108 | GGAAGGCTGAGGCGG[A/G]TGGATCACTTGAGTT | 5663 |
rs746087815 | snp | G/T | 1.64819e-05 | 0.00287066 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186929 | ACTTGGGGTAAGTTG[G/T]GAAATTTTTGGTCTG | 5663 |
rs746115413 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73159893 | AGTGGCATGATCTTG[G/T]CTCATGGCAGCCTTC | 5663 |
rs746122555 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73205698 | CAAATTTCCCTCCAG[G/T]GGGGATTATACCATT | 5663 |
rs746164478 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73193708 | GTCACCCAGGCTGGG[A/G]TGCAGTGGCACAGTC | 5663 |
rs746202334 | in-del | -/CCTATAATCCCA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73168095 | GTGCGGTGGCTCACT[-/CCTATAATCCCA]GCACTTTGGGAGACC | 5663 |
rs746270612 | snp | C/T | 3.29951e-05 | 0.00406159 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217095 | GCAAAGAGTGACCAA[C/T]TTTTTAATATTTGTA | 5663 |
rs746315817 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194475 | TGTGTTTCCCAGGCT[C/T]GTCCGGAACTCCTGG | 5663 |
rs746347339 | snp | C/T | 1.71971e-05 | 0.00293227 | utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73147969 | TTTCCCTTTTCAGAA[C/T]CTCAAGAGGCTTTGT | 5663 |
rs746365175 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73180391 | CAAGTCTTAGCACAC[A/G]CAAACAATTATATAG | 5663 |
rs746371742 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73148357 | TCCCAAGGTGTGCAG[C/T]GCCTCATAGTTCATG | 5663 |
rs746388216 | snp | A/G | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134808 | GCTGGAATTACAGGC[A/G]TGAGCCACCGCACCC | 5663 |
rs746441580 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73170632 | TTCAGTGAACAATGA[C/T]AGATAATCTAGACTT | 5663 |
rs746478880 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73168217 | AAAAATTAGTTGGGC[A/G]TGGTGGTGGGCACCA | 5663 |
rs746495189 | in-del | -/TT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73217795 | CTTTCAAAACTATGA[-/TT]TTTTTTTTTTTTTTT | 5663 |
rs746538194 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73198994 | TGCCCAGGCTGGTCT[C/T]GAACTCCTCGGCTTA | 5663 |
rs746560184 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73201127 | AGAGTCTTGCTGTGT[C/T]GCCCAGGCTGGAGTT | 5663 |
rs746575037 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73154033 | ATTTTCTTACAAATA[C/T]TAATTATTGAAAAAA | 5663 |
rs746593540 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73154923 | AAATAGGCTTTCTTG[C/T]ATGCTGTGTTCTTTG | 5663 |
rs746616948 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73204008 | TTTATTTTTTATTTT[-/A]TTTTTTTGAGACAGA | 5663 |
rs746638387 | snp | A/C | 2.1688e-05 | 0.00329295 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148150 | TGCCAGACTGGATTC[A/C]CTTATCATCTCCCCT | 5663 |
rs746663657 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73173234 | CTGTGGCAGAATCTG[G/T]TTCTATAACAAGTTC | 5663 |
rs746691776 | snp | C/T | 0.000115956 | 0.00761346 | missense | PSEN1 | GRCh38.p7 | 14:73170812 | AATGACAATAGAGAA[C/T]GGCAGGAGCACAACG | 5663 |
rs746698332 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73142989 | CTCAATTCGGGTCCC[A/G]TGAAAGATCCTCAGA | 5663 |
rs746828281 | snp | C/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221548 | AAGTTTGAGCCACAT[C/G]TCAGCCACATTGTTA | 5663 |
rs746839057 | snp | G/T | 1.66432e-05 | 0.00288467 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73206432 | AGGAGACCCGGAAGC[G/T]CAAAGGAGAGTATCC | 5663 |
rs746928210 | in-del | -/GTTT | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134491 | TATTGTACCACATTT[-/GTTT]ATTTATTTATTTATT | 5663 |
rs746937343 | snp | A/C | 1.64784e-05 | 0.00287035 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73186906 | GCTGTTCTTTTTTTC[A/C]TTCATTTACTTGGGG | 5663 |
rs746937948 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73176891 | TTACGTAAGATTCCT[A/C]TCAAATTCAGTCCTC | 5663 |
rs746975769 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209279 | AGCTGCACCTCCCCT[A/G]CTGCAGCTGCCATCT | 5663 |
rs747007019 | in-del | -/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73138939 | GCCACTGCACTCCAG[-/C]CTGGGCGACAGAGCC | 5663 |
rs747009241 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73164398 | AATACCCTAAGAGGA[A/G]ATCAGTTATACCTTG | 5663 |
rs747050462 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73206531 | CTGTTATAAGCTAAC[A/G]GTATAGCAATGTTTT | 5663 |
rs747058379 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73141265 | AATATTGGCTGAATA[A/C]TAATCTAATCTACCA | 5663 |
rs747095806 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73139055 | TTGGGAGGCCGAGGC[C/G]GGTGGATAACCAGAT | 5663 |
rs747136729 | in-del | -/TATTTATTTATTTTTA | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134523 | ATTTATTTATTTATT[-/TATTTATTTATTTTTA]TTTTTTGAGACATAG | 5663 |
rs747153673 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73198458 | GTCTTTCTGCTATTC[A/G]GTGACCACTGGGGAA | 5663 |
rs747160889 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73150892 | TCAACATGGTGAAAC[A/C]CCGTCTCTACTAAAA | 5663 |
rs747190647 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73160111 | TTATGGGTGTGAGCC[A/G]TCATGCCCAGCTGGC | 5663 |
rs747213199 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73170610 | TAAAAGAGAGGACCT[C/G]AATGCCTTCAGTGAA | 5663 |
rs747224464 | snp | C/T | 1.64982e-05 | 0.00287208 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217091 | CATAGCAAAGAGTGA[C/T]CAACTTTTTAATATT | 5663 |
rs747228477 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73215848 | TCAATTGTTGCTGGT[A/G]GAAATTCAGACTGGT | 5663 |
rs747249772 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73139611 | GGGGGGCAAAAAGAA[A/G]CAGATGAAACCAATG | 5663 |
rs747277987 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73204466 | CAAACTACTGCTTGA[A/G]GCCAAATATGGCCCA | 5663 |
rs747281728 | in-del | -/CCTT | 4.9552e-05 | 0.0049773 | frameshift-variant | PSEN1 | GRCh38.p7 | 14:73170830 | AGGAGCACAACGACA[-/CCTT]GACGGAGCCTTGGCC | 5663 |
rs747296392 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73171765 | ATGGAAAAACATTGC[C/T]TTACGAGGAAGTTAA | 5663 |
rs747311586 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73195197 | ATTTTTTTTGAGATA[C/G]AGTCTCGCTTTGTTG | 5663 |
rs747330597 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73216659 | ACCTACTCAGGAGGC[G/T]GAGACAGGAAAGTCG | 5663 |
rs747363386 | snp | A/G | 1.64738e-05 | 0.00286995 | missense | PSEN1 | GRCh38.p7 | 14:73173669 | ATTGTTGTCATGACT[A/G]TCCTCCTGGTGGTTC | 5663 |
rs747429980 | snp | A/C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73157900 | CTGAGACATGAGGAT[A/C/T]GCTTGAACCCAGGAG | 5663 |
rs747493312 | in-del | -/AG | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167152 | GTATATGGTACCAGC[-/AG]CACCTGATTATGCCA | 5663 |
rs747495809 | snp | A/G | 1.65176e-05 | 0.00287376 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192911 | CAGGAATGCCCCACT[A/G]GAGTGTTTTCTTTCC | 5663 |
rs747512101 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73159759 | CCATTGAACAACTCC[C/G]CATTTTCCATTTCTC | 5663 |
rs747539170 | in-del | -/CTT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73164850 | TACTTTAGGAACTTG[-/CTT]CTTTTATTTTCATAT | 5663 |
rs747615518 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73178989 | GTTGAGGATCATATC[C/T]ATACTCACTCACCTT | 5663 |
rs747620948 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73166328 | ATGGCTGTGGTGCCA[C/T]AGAAAGAAAACAAGT | 5663 |
rs747622052 | in-del | -/AG | 1.65217e-05 | 0.00287412 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211739 | ATTTTTCTAAATATT[-/AG]AGAGCTGTAACTTCC | 5663 |
rs747628009 | in-del | -/GTAATC | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73163320 | CGATGGCTCATGCCT[-/GTAATC]CCAGCACTTCGGGAG | 5663 |
rs747670633 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73180237 | TGATCCACTGGTTTC[A/G]GCCTCCCAAAGTGCT | 5663 |
rs747690556 | snp | A/C | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221540 | CTTTCTCCAAGTTTG[A/C]GCCACATCTCAGCCA | 5663 |
rs747715229 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73193551 | CGAGACTCTGTCTCA[-/A]AAAAAAAAAAAAAGC | 5663 |
rs747750345 | snp | G/T | 5.44549e-05 | 0.00521771 | missense, intron-variant | PSEN1 | GRCh38.p7 | 14:73148106 | TACTGTACGTAGCCA[G/T]GTACAGTGTCAGTCT | 5663 |
rs747751530 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167524 | CTCATGACCCAGTCA[C/G]CTCCTAAAGGCCTCA | 5663 |
rs747826221 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73168126 | TTTGGGAGACCGAGG[C/T]AGGTGGATCACCTGG | 5663 |
rs747828797 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73212889 | TTTTTGCAAGAGTGA[A/G]ACTTGATTAAAACAT | 5663 |
rs747830239 | in-del | -/CCCA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73198864 | CTGCAGCCTCGACCT[-/CCCA]GGCTCAGGTGATCCA | 5663 |
rs747835539 | snp | A/G | 1.66026e-05 | 0.00288115 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73206414 | GTTGGTGAATATGGC[A/G]GAAGGAGACCCGGAA | 5663 |
rs747869511 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73180609 | GGCAGTTAATTATTA[C/T]ACATAATTTGTTATA | 5663 |
rs747926350 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73188367 | ATTCCTTAATAAATA[A/G]ACGGGGTCGGGTGTG | 5663 |
rs747951311 | in-del | -/AGA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73198439 | TTGAGTGACTGGTTT[-/AGA]TGTCTTTCTGCTATT | 5663 |
rs747982416 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73141449 | CCAGAGGAGTCTTTT[G/T]AGGATGTATTCCTAA | 5663 |
rs748072584 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73142875 | TGAGATTAAGAAAAT[A/G]GATGTCAGTGAATTC | 5663 |
rs748115292 | snp | A/C | 1.64963e-05 | 0.00287192 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173721 | AGGTGAGCATGAGAC[A/C]CAGATCTTTGCTTTC | 5663 |
rs748202007 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73162995 | TGCTTTGCCTGCTTT[C/T]AAACAAATAAATTGT | 5663 |
rs748202331 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73161123 | GGAACTATAGGCACT[C/T]GCCACCATACCCACC | 5663 |
rs748260962 | in-del | -/AGA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73183645 | ACAGGATCCCAAGGC[-/AGA]AGAAGTTTTCTTAGT | 5663 |
rs748310681 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73149491 | GCACTGAATGGCGTG[A/G]AACTTCCTTTTACAC | 5663 |
rs748327218 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73195758 | TGGTGTTGACCTCCT[A/G]GCTTCAAGCAGCCTC | 5663 |
rs748336712 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73136987 | TGTCCTTGTCCAGGG[A/G]CGACGAGCATTCTGG | 5663 |
rs748344184 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73181684 | AAGCAGAATGTAAAC[A/G]GTACACTAGTTGATT | 5663 |
rs748397927 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73214153 | ACTTGGTTATAAAAA[G/T]AAACAATCTATCATT | 5663 |
rs748399922 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73214079 | AAACAGAAACAACCC[-/A]CATGTCTATTAACTG | 5663 |
rs748402429 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73150658 | GTAATCCCAGCTACT[C/T]CAGAAACTGAGGCAG | 5663 |
rs748427941 | in-del | -/TTG | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167065 | TTGAAATTCTTTTCA[-/TTG]TTGTTGTTGTTTTGA | 5663 |
rs748469097 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73182910 | CTTTGCCAAAAAACC[A/G]AGGTGAAAAGCATCT | 5663 |
rs748488045 | in-del | -/C | 4.94572e-05 | 0.00497254 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217112 | TTTTAATATTTGTAA[-/C]CTTTCCTTTTTAGGG | 5663 |
rs748522107 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73170452 | CTGAAATCACAGAAA[C/G]CTGAATTTGAAAAAG | 5663 |
rs748595733 | snp | C/T | 1.64974e-05 | 0.00287201 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219319 | GAATCCCATGGATGT[C/T]TCTTCTTTGACTATA | 5663 |
rs748605328 | snp | C/T | 3.30049e-05 | 0.00406219 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192905 | TTGTCACAGGAATGC[C/T]CCACTGGAGTGTTTT | 5663 |
rs748608184 | snp | C/G | 1.6473e-05 | 0.00286988 | missense | PSEN1 | GRCh38.p7 | 14:73192701 | TGTTGCACTCCTGAT[C/G]TGGAATTTTGGTGTG | 5663 |
rs748644735 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73171509 | TTACTTCTATATAGA[A/G]GGGTGCACCCTTACA | 5663 |
rs748692360 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219340 | TTTGACTATAACAAA[A/G]TCTGGGGAGGACAAA | 5663 |
rs748708439 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73152338 | AAAAAAGGCCAGGCA[-/T]GGTGGCTCACACATG | 5663 |
rs748715516 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73144889 | TATTTATATACCATT[A/T]ATTTATTTTATTTTA | 5663 |
rs748758065 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73205193 | TAAAATTACTGTGAC[A/C]AGGCCGGGCGTGGTG | 5663 |
rs748758205 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73192367 | GACCACCTGATCTCC[A/G]GAGGTAAAGACTGCA | 5663 |
rs748796275 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73145681 | GAAAGTGAACTTGTA[C/T]GGATACTCAAAAAGT | 5663 |
rs748809392 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73193381 | GAAACCCCGTCTCTA[C/G]TAAAAATACAAAAAT | 5663 |
rs748812628 | in-del | -/TTTTTTTTTTTTTTTT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73212089 | TATCAGTAATAGTGC[-/TTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 5663 |
rs748848893 | snp | A/G/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222958 | TGGTTTTGCCCTTGG[A/G/T]CTGGAAACTATCATA | 5663 |
rs748891711 | snp | A/T | 1.73751e-05 | 0.00294742 | missense | PSEN1 | GRCh38.p7 | 14:73198088 | TGGTTGAAACAGCTC[A/T]GGAGAGAAATGAAAC | 5663 |
rs748954676 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73178824 | TGTTTTATTGGCCAA[C/T]TGATCTGATTGGGCT | 5663 |
rs748966974 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221169 | TCACAGACAGGAAAA[A/G]TAAGAGCTATGCAAA | 5663 |
rs748973875 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73210457 | TCTTCTCTATAGGAG[A/G]TGAATAAGTACCTCA | 5663 |
rs748973954 | snp | A/T | | | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73224000 | CATAAGAAAGTGGTA[A/T]GGATTATAGCACACC | 5663 |
rs749014459 | in-del | -/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73147046 | GAGTCAGCCATTCTT[-/C]TTTTTTTTTTTTTTC | 5663 |
rs749054041 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167976 | CCTGGAACTGCAACC[C/T]TAAGTGAAAACAGCT | 5663 |
rs749063698 | in-del | -/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167847 | TTTTTTTTTTTTTTT[-/G]CTTCGAAGAATGATT | 5663 |
rs749093893 | snp | A/C | 1.70194e-05 | 0.00291709 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171077 | TGTTTTATTATTCTC[A/C]AAGCCAGTGTGGCTT | 5663 |
rs749201327 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73216975 | TAGAAAACCAAAAAA[G/T]AAAGAAAACACAGCT | 5663 |
rs749242671 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73141356 | ATGTATCACTACCCT[C/T]GCTCTTTTTAGCGTC | 5663 |
rs749249788 | snp | A/C | 1.64798e-05 | 0.00287047 | missense | PSEN1 | GRCh38.p7 | 14:73170959 | GCCAAGCATGTGATC[A/C]TGCTCTTTGTCCCTG | 5663 |
rs749312688 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73190595 | ATGAAATTAATAGTA[A/G]TGCTTTCCAATCAGG | 5663 |
rs749346953 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73189362 | ATGCCTGTAATCCCA[A/G]CACTTTGGGAGGCCG | 5663 |
rs749390584 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73159984 | CACTCTATCATGCCT[C/T]GCTAATTTTTTAATT | 5663 |
rs749432898 | in-del | -/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73208049 | TTGTGTTAACCTGGG[-/G]AACACAGGGGCACCC | 5663 |
rs749479033 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194725 | AGGCATCTGCCACCA[C/T]GCCCGGCTATTTTTT | 5663 |
rs749502194 | snp | A/G | 4.94189e-05 | 0.00497062 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73192674 | CTATAACGTTGCTGT[A/G]GACTACATTACTGTT | 5663 |
rs749513549 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73160733 | TTCTTTGAAGAAATA[C/T]CTGTTCAAGTCCTTT | 5663 |
rs749613267 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73144449 | TTTTTGAAGTTTAAG[A/G]TCTCATTTACTTCTA | 5663 |
rs749658027 | snp | C/G | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135112 | CAAGCATGAGCACTT[C/G]TAAATGAACAAACTA | 5663 |
rs749666911 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73181515 | TGTAGACCCAGTTAC[G/T]TGGGACCCTGAGACG | 5663 |
rs749768065 | in-del | -/TC | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73214894 | CGATTATACCTAGTG[-/TC]TTTGAACGGTGAACT | 5663 |
rs749784719 | snp | C/T | 1.64787e-05 | 0.00287038 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217292 | TCTTAATGTCAAAAC[C/T]TTGATTACACAGTCC | 5663 |
rs749796948 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73170368 | AGAGTTGCTCTGGTC[C/T]AAACGCCTCTGACAC | 5663 |
rs749839564 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73214080 | AACAGAAACAACCCA[C/T]ATGTCTATTAACTGA | 5663 |
rs749845608 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73155225 | ACAGTAGGGTCTCTT[A/G]ACTAAACAGTTGGAC | 5663 |
rs749898897 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73215256 | GTGAGCCACTGTGCC[C/T]GGCCAAAAAAATTTT | 5663 |
rs749914221 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73139898 | TCACAACGCCTTGTA[C/G]GGTTTCTTGTTTAAG | 5663 |
rs750074618 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73205074 | TTCAGCTTCTTTGAT[G/T]GTGTGTTTCTTTCAT | 5663 |
rs750080931 | snp | C/T | 1.64742e-05 | 0.00286999 | missense | PSEN1 | GRCh38.p7 | 14:73211864 | AGTCATCTAGGGCCT[C/T]ATCGCTCTACACCTG | 5663 |
rs750141128 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73193209 | CAGCTACTTAGGAGG[C/T]TGAGGTGGGAGGATC | 5663 |
rs750183379 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73160187 | GACTTGCTTATTTTG[C/T]TTAGCATAATGTCCT | 5663 |
rs750201190 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73206177 | GCAGGTGCAGTTTGA[A/G]TACTACAGTAAACAT | 5663 |
rs750231525 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73178649 | TGTTGGTAAACCTAT[C/T]CAGTAAAATGTTTTT | 5663 |
rs750273239 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73190254 | CCTATTTGGGAGGCC[A/G]AGGTGGGAGGATCCT | 5663 |
rs750293732 | snp | G/T | | | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73223802 | AATTAGCCAGGCGTG[G/T]TGGTGGGCGCCTGTA | 5663 |
rs750299814 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73158309 | TCTATCTATCTATCT[-/A]ATCTATCTATCTATC | 5663 |
rs750348634 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73211257 | TACCATCACTAGTTT[A/G]TAGGCTTGGTCTTCA | 5663 |
rs750352441 | snp | C/T | 8.23608e-05 | 0.00641667 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73192806 | CATGGCCCTGGTGTT[C/T]ATCAAGTACCTCCCT | 5663 |
rs750387288 | snp | C/T | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134453 | AATTTTCATGACATT[C/T]TGTGAGGTGGGTGGA | 5663 |
rs750407129 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167299 | GTCTGAAATTCAAAG[G/T]GCTCCCAAATCTGAA | 5663 |
rs750455936 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73147034 | GGCTGGGAGTCAGGA[A/G]TCAGCCATTCTTTTT | 5663 |
rs750585566 | snp | A/G | 1.64738e-05 | 0.00286995 | missense | PSEN1 | GRCh38.p7 | 14:73192666 | TTTAAAACCTATAAC[A/G]TTGCTGTGGACTACA | 5663 |
rs750602143 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73141105 | AGATTGCATTGACCA[A/G]AGCAAGTCACATGAT | 5663 |
rs750657073 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73189236 | ATAAAATGATTGTTT[A/C]CTTTGTTTTAGAACT | 5663 |
rs750657232 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73201536 | CCAAAGGGAAGGTGC[A/G]TATGTGTGCATGCAT | 5663 |
rs750705611 | snp | C/T | 0.000118793 | 0.007706 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208963 | TCCCATGCTTGTCAG[C/T]ACCCAAAGTCCAGAG | 5663 |
rs750708163 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73219268 | TATGGACCAATTAGC[A/G]TTCCATCAATTTTAT | 5663 |
rs750710235 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73190613 | CTTTCCAATCAGGCA[C/T]GGTGGCTCACACCTG | 5663 |
rs750726999 | snp | A/G/T | 3.34522e-05 | 0.00408965 | intron-variant | PSEN1 | GRCh38.p7 | 14:73170793 | GTTTTTCTTGTGCTT[A/G/T]TAGAATGACAATAGA | 5663 |
rs750774944 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73174526 | GGCATGAGCCACTGC[A/G]CCCGGCCCTAAGTGG | 5663 |
rs750821984 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73156961 | CCACCACGCCTGGCC[-/T]TTTTTTTTAAAATGG | 5663 |
rs750839144 | in-del | -/TTTAT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73144890 | TTTATATACCATTTA[-/TTTAT]TTTATTTTATTTTAT | 5663 |
rs750857788 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220914 | AGCTATGCTGATCAG[A/G]CCGTAAGCGTTTATG | 5663 |
rs750857858 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73208132 | CCTGGCTTAGGGAAC[C/T]CCTGAGTCTGGACTC | 5663 |
rs750870919 | snp | C/G | 1.70519e-05 | 0.00291987 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206362 | GTGTCCAGTGCTTAC[C/G]TGGAATTTTGTCTTT | 5663 |
rs750927923 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73200683 | CAAGTACTTACCCCT[A/G]TTGTCAGTTTGTTGT | 5663 |
rs750981436 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73211848 | GGAAGCCCAGAGGGA[C/T]AGTCATCTAGGGCCT | 5663 |
rs751032088 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73150439 | TTTATGTACATAAAT[C/T]GTATCGCATTATGTA | 5663 |
rs751033946 | snp | C/T | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136245 | ATATAGGGGCTTTCG[C/T]CCTCAGCTCGAGCAG | 5663 |
rs751038491 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73196406 | TTATATTATAGTTCT[A/G]TATATACTATATTAT | 5663 |
rs751092037 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73182287 | GAGTTCAAAACCAGC[C/T]TGGGCAACAGAGTGA | 5663 |
rs751112429 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73189478 | TTAGCCGGGCGTGGT[A/G]GTGGGTGCCTGTAAT | 5663 |
rs751134123 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73159858 | GACAAGATCTCACTC[C/T]GTTGCCCAGGCTAGA | 5663 |
rs751137344 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73214799 | GGGAAATGAAGGGTC[A/G]TTTAATGGGTGTAGA | 5663 |
rs751244435 | snp | C/G | | | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137515 | CAATTCCATAGATTT[C/G]CAGTTGATGTTGGAG | 5663 |
rs751246420 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73203223 | AGCTGGGATTACAGA[C/T]GCCTGCCACCACGCC | 5663 |
rs751252276 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73169974 | GGGGTGGATTATTCA[G/T]GAGTTTTCTGGGAAA | 5663 |
rs751258598 | snp | C/G/T | 3.29491e-05 | 0.00405877 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211760 | TGTAACTTCCACTTT[C/G/T]TCTTGAAGGCACAGA | 5663 |
rs751268000 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73203809 | GAGGTAGATCATTTT[A/G]TCTAAAGCTTTTTGA | 5663 |
rs751291382 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73143989 | GAGACCTTGTCTCTT[-/A]AAAAAAAAAAAAAAA | 5663 |
rs751321652 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73179991 | CTTCATTTTATTTTA[-/T]TTTTTTTTTTTGAGA | 5663 |
rs751378088 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73205058 | AATAACAAGGTGGTC[A/G]TTCAGCTTCTTTGAT | 5663 |
rs751422740 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73211069 | GGGATGAGTGCCAAC[A/G]GTTAGGAAGCTTTCA | 5663 |
rs751432648 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73147664 | TATAGTAAATTTGTC[-/A]AGTTAGTTGAAAGTC | 5663 |
rs751442372 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73157469 | TTTAAAAACAGCTTT[A/G]TTGTGGTATAATTGA | 5663 |
rs751468503 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73189973 | AGCCAGTTGTAGGCC[A/C]ACAACGGGGTGGAGG | 5663 |
rs751481989 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73193129 | AGCCTGGGCAACATG[A/G]CAAAACCTCGTATCT | 5663 |
rs751542268 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73168837 | CACCTGGCCATCCCC[A/G]AATGGCCGCGTTGAA | 5663 |
rs751557514 | in-del | -/CTAAT | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221369 | ATTCTTGAGGGATCC[-/CTAAT]CTAGAGTAATTTATT | 5663 |
rs751659957 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73179388 | TTGGGAGGCCAAGGC[A/G]GGCAGATTGCCTGAG | 5663 |
rs751736200 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73177978 | ACTCTTTTTTTTTTT[G/T]AAACAGAGTGGCGCA | 5663 |
rs751800891 | snp | A/G | 1.77798e-05 | 0.00298154 | intron-variant | PSEN1 | GRCh38.p7 | 14:73170759 | CTTGATTCTGCTGAG[A/G]ATCTGATTTACTGAA | 5663 |
rs751806512 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73212441 | AGTTGGCATTTTACA[A/G]CCTGACCTTTTGGCA | 5663 |
rs751812693 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73199713 | TTCCCTTCAGTAATA[C/T]GAAAGTATCAATTTC | 5663 |
rs751858492 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220921 | CTGATCAGACCGTAA[A/G]CGTTTATGAGAAACT | 5663 |
rs751916030 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73187929 | ATTCAGCAATAGATG[A/C]AAAGAATAATACTTT | 5663 |
rs751937012 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73200563 | TCCCAGCCCTGTAAA[A/C]TTAATCTTAATTATA | 5663 |
rs751974771 | snp | C/T | 1.7227e-05 | 0.00293482 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206346 | TCTATGCATACTTTG[C/T]GTGTCCAGTGCTTAC | 5663 |
rs752037124 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73152147 | CGGATCTCCTGACCT[C/T]GTGATTCGCCCGTCT | 5663 |
rs752088586 | in-del | -/TTTTT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73158071 | ATGTTATGTGGTTCC[-/TTTTT]ATTGCTGAGTTGTAT | 5663 |
rs752156635 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73174417 | TTTTGTATTTTTAGT[A/T]GAGACAGGGTTTCAC | 5663 |
rs752158054 | in-del | -/GCGGCCCGTTTCTCGGGCTTCGGGC | | | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136754 | GGGAAACCAGGAGGG[-/GCGGCCCGTTTCTCGGGCTTCGGGC]GCGGCCGGGTGGAGA | 5663 |
rs752205606 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73208022 | GCCACAAGCCTGGCT[C/G]TTGTGTTAACCTTGT | 5663 |
rs752229499 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194882 | CTGGCCATACACTTT[C/T]GTCATTATTTACATA | 5663 |
rs752259177 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73195150 | GAGACAGAATGTCTG[C/G]GTTCAAATTCTACTC | 5663 |
rs752283032 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73196179 | AAGCAATTTTAATTT[A/G]ATTGCTCTAAAAAAT | 5663 |
rs752304817 | snp | A/G | 1.99118e-05 | 0.00315523 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206512 | TCTTGATTTTTCAGG[A/G]TCACTGTTATAAGCT | 5663 |
rs752333150 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73148973 | AATAGAGAAAAAGAA[A/C]GAAAAGAAAAGAGAG | 5663 |
rs752418925 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73208243 | CCCTGTTTGTCTTAC[A/G]GTTCTTTCAATCCTG | 5663 |
rs752431117 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73213772 | CTCAGCATCATTAGC[C/T]ATCAAGGAAATGCAA | 5663 |
rs752439716 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73181964 | TTTTTAGTAGAGACG[A/G]GGTTTTGGCATGTTG | 5663 |
rs752488170 | snp | A/G | | | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137623 | GAAGAAGAGCAAGGA[A/G]CCAGCTGAGGAGAAT | 5663 |
rs752515599 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73143316 | GCTCACCTTGTAGCA[C/T]TGTGATCTTTGGAAG | 5663 |
rs752574021 | in-del | -/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73210739 | AATTGTGAGGGCTCT[-/C]CCCAGAGGAAGCCAT | 5663 |
rs752589792 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73157272 | CTGGGATTACAGGCA[C/T]GCACCACCACACCCA | 5663 |
rs752615160 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73210645 | TCTTATTCTTATATT[A/T]TTTCATAAACTCCAA | 5663 |
rs752659541 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73190761 | GAGGGGAACCATGGG[A/G]CACAGTGGGGAGAAA | 5663 |
rs752665713 | snp | A/G | 3.43218e-05 | 0.00414243 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211988 | TGGATTCCTTTAGGT[A/G]GCTACATTATCAACC | 5663 |
rs752675583 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73196506 | TTTTTTTTTGAGGCA[C/G]GGTCTTACTTTGTCA | 5663 |
rs752679562 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73191811 | CCTCAGCCTCCCAAA[C/T]TGCTGGGATTAGAGT | 5663 |
rs752692203 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73143874 | CACCCATGTAGTCCC[A/G]CCTGCTTGGGAGGCT | 5663 |
rs752737031 | in-del | -/A | 1.72689e-05 | 0.00293839 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173816 | AATGTTTTGTCTTCT[-/A]GAGATAAGTTAATTT | 5663 |
rs752833058 | snp | A/T | 3.5014e-05 | 0.00418399 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73198059 | TTTGTGTCCGAAAGG[A/T]CCACTTCGTATGCTG | 5663 |
rs752868093 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194694 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 5663 |
rs752881318 | snp | C/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222511 | CTTTGATCCCAACCC[C/G]CAAGGCTTTGTATAT | 5663 |
rs752960190 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73177479 | TTACAGGCGTGAGCC[A/G]CTATGCCAGGACAGC | 5663 |
rs752965443 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73164255 | GAGAAGCTTAGAATA[G/T]AGTTCTAGGAGAGGT | 5663 |
rs752980679 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73197700 | ACAACTGCTTAAAAT[A/C]GTCTATCTCATCATT | 5663 |
rs752988760 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73168355 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAACAA | 5663 |
rs753010568 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73199236 | TTTGAGATAGAGACT[C/T]GAAGAACATTAGCAG | 5663 |
rs753057990 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73198313 | TGATGTTGATTCAAG[A/C]GAGTTTTCAATATGA | 5663 |
rs753131102 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73139528 | GAGGTTGCAGTGAGC[C/T]GAGATCATGCCACTG | 5663 |
rs753147329 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73175269 | GTAGCTGGGATTACA[A/G]GCGCCTGCCACCACA | 5663 |
rs753155164 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73205350 | CAGGCATGGTGGCGG[C/G]CGCCTGTAGTCCCAG | 5663 |
rs753191324 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73187766 | AATACTAAGTGTTCC[A/G]AACATATAAAAAGAA | 5663 |
rs753239924 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73216994 | GAAAACACAGCTGAA[A/G]CCTAATTTTGTATAT | 5663 |
rs753243035 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73153320 | GCACAAATATTAATA[A/C]TATGTTAAGAAACTT | 5663 |
rs753246918 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73172343 | TTAGCCTTTTGGGAG[A/C]GCATCTAAGACAGCA | 5663 |
rs753259560 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73140797 | TTTTATTGCATTTTC[C/T]GAGCCAACATAACCA | 5663 |
rs753297180 | in-del | -/TTTATTTATTTATTTAT | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134489 | ATTTATTGTACCACA[-/TTTATTTATTTATTTAT]TTATTTATTTATTTA | 5663 |
rs753340509 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73217949 | CCTGCCACCACGCCC[A/G]GCTAATTTTTGTATT | 5663 |
rs753402219 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73206344 | TGTCTATGCATACTT[C/T]GTGTGTCCAGTGCTT | 5663 |
rs753413086 | in-del | -/AAACCTATAACGTTGC | 1.64876e-05 | 0.00287116 | frameshift-variant | PSEN1 | GRCh38.p7 | 14:73192655 | TCAGGGAAGTGTTTA[-/AAACCTATAACGTTGC]TGTGGACTACATTAC | 5663 |
rs753444183 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73147932 | TAACAGTATAATTGT[A/G]GTGCACAAAGTTCTG | 5663 |
rs753457678 | snp | G/T | 1.64768e-05 | 0.00287021 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73173686 | CCTCCTGGTGGTTCT[G/T]TATAAATACAGGTGC | 5663 |
rs753510892 | snp | A/G | 1.64836e-05 | 0.0028708 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186818 | TTTAAGGGTTGTGGG[A/G]CCTGTTAATTATATT | 5663 |
rs753522012 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73146714 | AGAAGAAAAAAAATG[C/G]AATATTTAGAGGAAA | 5663 |
rs753526685 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194349 | CTCAAACCCTTGTCC[C/T]GGGCTCAAACAATCC | 5663 |
rs753606005 | in-del | -/ATTT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73166994 | ACCGCAGACTGGGTG[-/ATTT]ATTTATTTATTTATT | 5663 |
rs753641146 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73165606 | ACAAAAAATTAGCCA[A/G]GCATGGTGGCGCATG | 5663 |
rs753648250 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194996 | TGGTTCTGTTCTTGT[A/G]TTTGAGTAATCAGTT | 5663 |
rs753667906 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73185015 | AGACGATGGGCGGCC[A/G]GGCAGAGACGCTCCT | 5663 |
rs753684066 | snp | A/G | 1.68131e-05 | 0.00289935 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211974 | ATGTTGCAAAGTCAT[A/G]GATTCCTTTAGGTAG | 5663 |
rs753702410 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73212734 | GGATTTAAGTTAACA[C/G]TTAGGGCTTCTTAGG | 5663 |
rs753727542 | in-del | -/ATAGGACC | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73140133 | ATTATACAAAGGTAT[-/ATAGGACC]ATAGTCTCATATCCA | 5663 |
rs753753730 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73213567 | TGTGAGCATGTTAAA[C/T]CAGACTTGTGGGTAC | 5663 |
rs753772341 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73169570 | CTTATCTCTACCAAT[C/G]CTAGTTCCTTATGCT | 5663 |
rs753790723 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73200832 | TAGGTGGGCGGATCA[C/T]TTGAGGTCAGGAGTT | 5663 |
rs753804016 | snp | C/T | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135968 | TCTCAGCTAGCTTGC[C/T]ACCTAGAAAGACTGG | 5663 |
rs753813529 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73168627 | TTCAGGGAAAGATCA[C/G]CTTCTTCCCATACCA | 5663 |
rs753821973 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73201798 | GTTGCTCGGGCTAGA[A/G]TGCAGTGGTGTGATC | 5663 |
rs753839679 | in-del | -/GC | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73140196 | GGTTTTTCTTTTTTT[-/GC]TATTCTTTTTTTTTT | 5663 |
rs753875361 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73190657 | TTTGGAGGTGGAGAC[A/G]GGAGGACTGCTTGAG | 5663 |
rs753894928 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73151827 | ACATGTCTTGGCCTC[A/C]CAAAGTGCTGGGATT | 5663 |
rs753950364 | in-del | -/CT | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219952 | TCTCAAGCACTGACA[-/CT]CATTACCGTCTGTGA | 5663 |
rs753954632 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73142598 | AGAGAAGAAAACGTA[C/T]TAATTCTTTTCTGTT | 5663 |
rs753956530 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73155756 | ACTCCTGGGCTCAAG[C/T]GATTCTCCCGTCTCG | 5663 |
rs753958763 | in-del | -/GA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73162476 | TCTCCATGAGAAGGA[-/GA]GAGAGAGAGAGAGAG | 5663 |
rs753988847 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73149398 | GTACATTTCACTACA[A/G]ACAGTCACAAAAGGC | 5663 |
rs754037857 | snp | C/T | 1.64749e-05 | 0.00287005 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73192848 | GTGGCTCATCTTGGC[C/T]GTGATTTCAGTATAT | 5663 |
rs754063709 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221002 | CTGTTTTCTCTCCCA[A/G]TCTATGATATGATAT | 5663 |
rs754080097 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73191544 | AATACGTACATATAT[A/T]TTTTTTTTCTTTTCT | 5663 |
rs754084958 | snp | A/G | 1.64819e-05 | 0.00287066 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73171015 | GGCTACCATTAAGTC[A/G]GTCAGCTTTTATACC | 5663 |
rs754103115 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222289 | AAGAGGCAGTGTTTT[C/T]ACTTTCAGACTCCGG | 5663 |
rs754146691 | in-del | -/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73202418 | AATATCTATCACATA[-/C]TATATATATATATAT | 5663 |
rs754156805 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73176226 | CCAAAAAGCAAGTGA[C/T]ATAAACCCATGCTGG | 5663 |
rs754180265 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209035 | AAGCGCCCGCACACC[C/T]GGCCAGGTCATGACA | 5663 |
rs754379992 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73186429 | GTACCAATATCTAGG[C/T]AAAGCCATTCTGTTG | 5663 |
rs754391762 | snp | A/G | 1.64836e-05 | 0.0028708 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211746 | CTAAATATTAGAGCT[A/G]TAACTTCCACTTTCT | 5663 |
rs754392688 | snp | A/G | 3.29794e-05 | 0.00406061 | missense | PSEN1 | GRCh38.p7 | 14:73170876 | CTAATGGACGACCCC[A/G]GGGTAACTCCCGGCA | 5663 |
rs754432497 | snp | A/G | | | missense | PSEN1 | GRCh38.p7 | 14:73206442 | GAAGCTCAAAGGAGA[A/G]TATCCAAAAATTCCA | 5663 |
rs754448863 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73182355 | AAAATTAGCCAGGCA[G/T]GGTGGTGTACCCACG | 5663 |
rs754450453 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73146800 | TGTAAATGTGTATAT[A/G]GTAATGTATTAATTA | 5663 |
rs754537407 | snp | C/T | 1.67961e-05 | 0.00289789 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206380 | GAATTTTGTCTTTCC[C/T]AACAGCAACAATGGT | 5663 |
rs754550518 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73160340 | ATACTGAATAATGCT[A/G]TGGTGAAAGTGGCTA | 5663 |
rs754576920 | snp | A/G | | | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73224063 | TATAAAAGCCCCAAA[A/G]CAGCTATCCTTAATA | 5663 |
rs754577660 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194389 | AGCCTTCAAAGTAGA[C/T]AGAACTACAGGCATG | 5663 |
rs754698746 | in-del | -/GAGA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73162474 | TCTCTCCATGAGAAG[-/GAGA]GAGAGAGAGAGAGAG | 5663 |
rs754739855 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73168083 | CAGCTGGGCTGGGTG[C/T]GGTGGCTCACTCCTA | 5663 |
rs754748239 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73140250 | GAGTCTCCCTCTGTC[A/G]CCCAGGCTGGAGTGC | 5663 |
rs754756568 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73212825 | GAGATGTGGTTCATT[A/G]AATAAGACTTTAGCA | 5663 |
rs754757663 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73181284 | GTCTCTACTAAAAAT[A/G]CAAAAAAATTAGCTG | 5663 |
rs754807877 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73213728 | TCCCAAGAAAATGTA[A/C]AAATGATCTGTAAAC | 5663 |
rs754858106 | in-del | -/TTC | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167031 | TTGTTGTCATTTGTT[-/TTC]TTCTTTTTTGTATCT | 5663 |
rs754892375 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73189440 | ACGTGGTGAAAACCC[A/G]CCTCTACTAAAAATA | 5663 |
rs754906715 | in-del | -/GT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73191400 | TGTGTATGTATAAGT[-/GT]GTGTGTGTGTGTATG | 5663 |
rs754947622 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73205866 | AAGGGGCACAGAGGA[A/G]GCCTCTTGACTATCC | 5663 |
rs754965610 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73201900 | TATAGGCACCCACCA[C/T]CACATCCGGCTAATG | 5663 |
rs755016826 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73190717 | ATAGCAAGACCCCAT[C/T]TCAAGAAAAAGTAGT | 5663 |
rs755074105 | in-del | -/TT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73147599 | TTGTGGTTGAAAATG[-/TT]TGGTGTCTCAGGCGG | 5663 |
rs755161318 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73174764 | AACTGGTAGCCACCA[A/T]GCATCCTCTCACCAT | 5663 |
rs755161885 | snp | C/T | 1.64762e-05 | 0.00287016 | missense | PSEN1 | GRCh38.p7 | 14:73192850 | GGCTCATCTTGGCTG[C/T]GATTTCAGTATATGG | 5663 |
rs755184558 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73208236 | GTTTCAGCCCTGTTT[A/G]TCTTACGGTTCTTTC | 5663 |
rs755230833 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73162750 | AAAATGCTGCATGGT[A/G]CATTTACTGTACTAC | 5663 |
rs755281395 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73149408 | CTACAAACAGTCACA[A/T]AAGGCTGAAAGGCCA | 5663 |
rs755286234 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73162694 | CTTTATGTACTGATG[C/T]GTAGAAAAATCTCTA | 5663 |
rs755316785 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194621 | TCGCCCAGACTGGAG[C/T]GCAGTGGCGTGATCT | 5663 |
rs755341146 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73164253 | AGGAGAAGCTTAGAA[C/T]AGAGTTCTAGGAGAG | 5663 |
rs755366428 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209764 | AATAGGGGACGGCCC[A/G]CTGAAGGATGGAGGA | 5663 |
rs755381181 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73182732 | TAATCCCAGCTACTC[A/G]GGAGGCTAAGGCAGG | 5663 |
rs755398046 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73213993 | GGTATATACTCAAGA[G/T]AATTTTAAAACATAT | 5663 |
rs755402092 | snp | A/G | 1.64898e-05 | 0.00287135 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73170877 | TAATGGACGACCCCA[A/G]GGTAACTCCCGGCAG | 5663 |
rs755426929 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73192005 | AGGTATGATATGATC[-/T]TTTTTCCTCTTCGTA | 5663 |
rs755460394 | snp | G/T | | | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137941 | GGCGTGGGGGCGCGC[G/T]CCTGTAGTCCCAGCT | 5663 |
rs755507479 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73186446 | AAGCCATTCTGTTGG[C/G]CTTTGCCAAATTGTA | 5663 |
rs755522921 | in-del | -/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73195345 | GCCCAGCTAATTTTT[-/G]TATTTTTAGTAGAGA | 5663 |
rs755634855 | snp | C/G | 1.64754e-05 | 0.00287009 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73173680 | GACTATCCTCCTGGT[C/G]GTTCTGTATAAATAC | 5663 |
rs755660573 | in-del | -/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73182304 | GGCAACAGAGTGAGA[-/C]CCCCCACCTCTACAA | 5663 |
rs755710446 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73172222 | AATGTCATCTAGTTC[C/G]ATCTCTACGACTCTC | 5663 |
rs755765273 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73159481 | TTTTACATTAGGTCT[G/T]TGATCCTTTTGAAGT | 5663 |
rs755782675 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73145374 | GGGTCTCACTCTGTC[A/G]CTCAGGCTGGAGTGT | 5663 |
rs755798506 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194104 | CCTGAACAGTTAGAA[C/G]ATACTCCAGCCATTA | 5663 |
rs755804951 | in-del | -/T | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134883 | TATTCCATGAATATC[-/T]TTGCCCAAAATTTTT | 5663 |
rs755812612 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73193275 | TGATTGCATCACTGT[A/G]TTCCAGCCTGGGTGA | 5663 |
rs755855885 | in-del | -/T | 3.30074e-05 | 0.00406234 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186964 | TCAGAATTAACTACC[-/T]TTGTGCTGTGTAGCT | 5663 |
rs755878292 | snp | A/C | 1.64746e-05 | 0.00287002 | missense | PSEN1 | GRCh38.p7 | 14:73211865 | GTCATCTAGGGCCTC[A/C]TCGCTCTACACCTGA | 5663 |
rs755883961 | snp | A/G | | | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73223903 | AGATCTCACCACTGC[A/G]CTCCAGCCTGGGCGA | 5663 |
rs755917507 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73179710 | TAGAGGTCTTCTGGA[A/G]CTCCCATTGTCTTGC | 5663 |
rs755937539 | snp | A/C | 1.64727e-05 | 0.00286986 | missense | PSEN1 | GRCh38.p7 | 14:73211792 | AGGGAGTCACAAGAC[A/C]CTGTTGCAGAGAATG | 5663 |
rs755946947 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73146565 | AAAAGCATGTATGAT[A/G]AAGTGGAATGTCACC | 5663 |
rs755957699 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73166165 | AGTGTTCTAGTATCC[A/G]TCTCATTATCAGCCT | 5663 |
rs755968905 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73211286 | CAGCCCACTGCTCTT[C/T]GTGGTCATGACAGCT | 5663 |
rs755989181 | in-del | -/TTTT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73146185 | TAGTTTTAAAAAATC[-/TTTT]TTTTTTTTTTTTTTT | 5663 |
rs756010683 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167322 | AATCTGAAGCTTTCT[A/G]AGTATCAATGTGATG | 5663 |
rs756014036 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73200045 | AGCCACCATGCCCGG[C/T]CACTGCTTTGTTAAT | 5663 |
rs756015747 | in-del | -/AG | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73166974 | TTGTATTGCTATAAC[-/AG]AATACCGCAGACTGG | 5663 |
rs756031631 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73203772 | TGGGAGCTTAACTAG[-/A]AAGGGAAACTAACAA | 5663 |
rs756093611 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73212703 | CTTCAGTGTCTAAGA[C/T]GTGTTGCCACTTGAT | 5663 |
rs756168158 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73153648 | GTAGAAATTCAAACA[A/G]TATCCATTAAGTCAT | 5663 |
rs756211906 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73200775 | AAGGAGAGAGGCTGG[A/G]CGTGGTGGCTAACAC | 5663 |
rs756239069 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73142535 | GAATCAATAAGTAAC[C/T]ATGTTCTGCAGGAGT | 5663 |
rs756256461 | snp | A/G | 1.64732e-05 | 0.0028699 | missense | PSEN1 | GRCh38.p7 | 14:73192669 | AAAACCTATAACGTT[A/G]CTGTGGACTACATTA | 5663 |
rs756257939 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73154453 | AAAAAAAGTGAAAAT[C/T]AGTGGGGTGTGGTAG | 5663 |
rs756276340 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73218894 | TTTCAGATTCTATTT[C/G]TTTACTAGAATTAAG | 5663 |
rs756287473 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73141195 | ACAGAGCCAAGCCTA[C/T]AACATCACTGGAGAG | 5663 |
rs756309757 | snp | A/G | 4.94189e-05 | 0.00497062 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73192833 | CCCTGAATGGACTGC[A/G]TGGCTCATCTTGGCT | 5663 |
rs756373976 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73160684 | ACACAGATGTAGAGC[A/G]TCTTTTCATGTGCTT | 5663 |
rs756378615 | in-del | -/TTTCT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73196929 | AATTTTCTTTCTTTC[-/TTTCT]TTTTTTTTTTTTTTT | 5663 |
rs756405565 | in-del | -/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73184746 | CTGGCGGGGGGCTGA[-/C]CCCCCCCCACCTCCC | 5663 |
rs756436189 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73173465 | TGACTTATAAGATAC[A/G]AATTGAATTAAGAAA | 5663 |
rs756436265 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73190625 | GCACGGTGGCTCACA[C/T]CTGTAATCTCAACAT | 5663 |
rs756473262 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73213340 | ATTCTTTCATGACTG[C/T]CTTTTCTAATTTGAC | 5663 |
rs756485522 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73174617 | CTCATTCACAAATAA[C/G]ACTGTAGGATATAAT | 5663 |
rs756539660 | snp | A/T | 1.6477e-05 | 0.00287024 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206503 | TAGATAATATCTTGA[A/T]TTTTCAGGGTCACTG | 5663 |
rs756576165 | snp | C/T | 3.49394e-05 | 0.00417953 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73148094 | CCACCTGAGCAATAC[C/T]GTACGTAGCCAGGTA | 5663 |
rs756593202 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73143921 | CTGAGGCCAGGAGTT[A/C]AAGGCTGCAGTGAGC | 5663 |
rs756634054 | in-del | -/TTTT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73176301 | CCTTTTCTTTATCCC[-/TTTT]TTTGTCTGCACGTGT | 5663 |
rs756653817 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73182593 | TCACGCCTATAATCC[C/T]AGCACTGTGGGAGGC | 5663 |
rs756664503 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73181489 | TCACGCCAGGTGCAG[C/T]GGCACGGACCTGTAG | 5663 |
rs756696586 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73213901 | TGCTGGTGGGAATGT[A/G]AAATAGTATAGTGAT | 5663 |
rs756733594 | snp | C/T | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136275 | GCCTCAGAACCCCGA[C/T]AACCCACGCCAGCGC | 5663 |
rs756764981 | snp | A/G | 1.64735e-05 | 0.00286993 | missense | PSEN1 | GRCh38.p7 | 14:73211850 | AAGCCCAGAGGGACA[A/G]TCATCTAGGGCCTCA | 5663 |
rs756816679 | snp | A/G | 1.64841e-05 | 0.00287085 | missense | PSEN1 | GRCh38.p7 | 14:73170912 | TGGAGCAAGATGAGG[A/G]AGAAGATGAGGAGCT | 5663 |
rs756871556 | snp | C/T | 1.66524e-05 | 0.00288547 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171053 | ATGGGCAGCTGTACG[C/T]ATGAGTTTTGTTTTA | 5663 |
rs756889718 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73214881 | TAGCACAATGATACG[A/T]TTATACCTAGTGTCT | 5663 |
rs756920958 | in-del | -/AAT | 1.64982e-05 | 0.00287208 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192900 | TTTGTTTGTCACAGG[-/AAT]GCCCCACTGGAGTGT | 5663 |
rs757041405 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73203285 | TAGAGAGAGGGTTTC[A/G]CCATGTTGGCCAGGC | 5663 |
rs757096200 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73144322 | TGGGATTACAGGCGT[A/G]AGCCACTGCGCCCAG | 5663 |
rs757147759 | snp | C/T | 3.29527e-05 | 0.00405898 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73192662 | AGTGTTTAAAACCTA[C/T]AACGTTGCTGTGGAC | 5663 |
rs757154639 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73159925 | CCTCCTGGGCTCAAG[C/T]TGTCTTCCCACCTCA | 5663 |
rs757203995 | in-del | -/AAAG | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73148967 | TAAATAAATAGAGAA[-/AAAG]AAAGAAAAGAAAAGA | 5663 |
rs757221245 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223628 | ATTCTTGGTAAGATA[C/T]AATTTTGATAGCTGA | 5663 |
rs757234377 | in-del | -/TATCTATG | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73158300 | ATCTATCTATCTATC[-/TATCTATG]TATCTATCTATCTAT | 5663 |
rs757280377 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73190063 | CTCAGAGCTGCTAGT[A/G]CAGGCTGTGCAGAGG | 5663 |
rs757303271 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73165961 | CTCGGGAGGCTGACG[C/T]GGGAGAATTGCTTGA | 5663 |
rs757386254 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73196732 | TGCTGCCTCAGCCTC[C/T]CCAAAGTGCTGGAAT | 5663 |
rs757393518 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167251 | CTACTCCTGTGATAA[C/T]GACATTGCAGGTTCA | 5663 |
rs757395951 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73211186 | GCATTTGAAATTTGT[A/G]GGGTTGGTTAATTTG | 5663 |
rs757412529 | in-del | -/CT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73197662 | AGAAGTGACTTCTCC[-/CT]GTTTCTGCTCACTGT | 5663 |
rs757428219 | snp | C/T | 1.75394e-05 | 0.00296132 | intron-variant | PSEN1 | GRCh38.p7 | 14:73170771 | GAGAATCTGATTTAC[C/T]GAAAATGTTTTTCTT | 5663 |
rs757498785 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73172463 | ATTGGCAAGCTACAG[C/T]CACAGGCCAGATCTG | 5663 |
rs757506602 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73139621 | AAGAAACAGATGAAA[C/T]CAATGTGAATAATTT | 5663 |
rs757572307 | in-del | -/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73202048 | CACTGCACCCGACCT[-/G]TTTTATTTTATTTTT | 5663 |
rs757594313 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73218784 | TCTTCACCTCTGGGT[C/T]TTTAACCAGCCAAAC | 5663 |
rs757610546 | snp | C/T | 1.72018e-05 | 0.00293268 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206351 | GCATACTTTGTGTGT[C/T]CAGTGCTTACCTGGA | 5663 |
rs757637085 | snp | A/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221071 | GTTTTCTGTCCCAGG[A/T]TATTTCTTATAAGAA | 5663 |
rs757677948 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73159813 | TGTTTCTATAACATG[C/G]ACTACTTGAGTTTTT | 5663 |
rs757681015 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73166220 | TAATGTTCATTATAA[A/T]CCAGATCATCCAGTT | 5663 |
rs757697857 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73173430 | AAAATTCTTAGCTAG[A/T]TTGGTGAGTTGGGGA | 5663 |
rs757698754 | snp | G/T | 1.73579e-05 | 0.00294596 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73198074 | TCCACTTCGTATGCT[G/T]GTTGAAACAGCTCAG | 5663 |
rs757705689 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73211695 | TGACAGCTAGTTACT[A/G]TTTCCATGTAATTTT | 5663 |
rs757721893 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73208064 | GAACACAGGGGCACC[A/C]AGAAGCTTGGAGATG | 5663 |
rs757729385 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73160522 | ATTCCCACCAACAAT[A/G]CATAGTGGTTCCAAT | 5663 |
rs757744941 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73206560 | TTTATCGTCTTTCTT[A/T]GGTCATAGACTCCTT | 5663 |
rs757776517 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73175479 | AGACCTATCTCTACC[-/A]AAAAAAAAAAAAATT | 5663 |
rs757846618 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73195176 | TACTCATCACTTTTT[A/C]TTTTTATTTTTTTTG | 5663 |
rs757882529 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73148221 | TACTTTACCACATTT[A/G]TAATATATTTGGTGA | 5663 |
rs757938634 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73212956 | CACCTAGGTTCCTTA[A/G]CATCTTTAATCATTA | 5663 |
rs757999622 | in-del | -/CC | 1.70796e-05 | 0.00292224 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206360 | TGTGTCCAGTGCTTA[-/CC]CCTGGAATTTTGTCT | 5663 |
rs758024838 | in-del | -/GCTC | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73198869 | GCCTCGACCTCCCAG[-/GCTC]AGGTGATCCACCCAC | 5663 |
rs758038439 | snp | C/T | 1.64819e-05 | 0.00287066 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211747 | TAAATATTAGAGCTG[C/T]AACTTCCACTTTCTC | 5663 |
rs758116694 | in-del | -/ATTT | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134496 | GTACCACATTTATTT[-/ATTT]ATTTATTTATTTATT | 5663 |
rs758201010 | snp | A/G | 1.64779e-05 | 0.00287031 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73186885 | TATTATATCATCTCT[A/G]TTGTTGCTGTTCTTT | 5663 |
rs758210200 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73169766 | TTCTCCTGCCGTAGC[C/T]TCATGAGTAGCTGGG | 5663 |
rs758230211 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73190809 | TCTGTTGTGAATTTT[A/G]TATCTTATTCATGTG | 5663 |
rs758232241 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73203236 | GACGCCTGCCACCAC[A/G]CCCAGCTAATTTTTT | 5663 |
rs758294283 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73175054 | GGCCAGGCATGGTGG[C/G]TCATGCCTGTAATCC | 5663 |
rs758305644 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73187450 | ACAATTGCACTAGCT[C/G]TTAAATTCGAAGAGG | 5663 |
rs758415163 | snp | G/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221458 | AGGGTACGTGGGGTG[G/T]GTGTATTTAAATCCA | 5663 |
rs758419639 | snp | A/G | 1.75727e-05 | 0.00296412 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211994 | CCTTTAGGTAGCTAC[A/G]TTATCAACCTTTTTG | 5663 |
rs758424415 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73210705 | TGGATAATAAAAAGA[A/T]TACAAAACTATCAAT | 5663 |
rs758438382 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73176788 | GAGGCACTGAGGCAG[C/G]GGTCACACAGCTAGT | 5663 |
rs758473349 | in-del | -/TG | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73197828 | TTTTTACAGATGTTC[-/TG]TGTCATTTTATTTTG | 5663 |
rs758475342 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73145142 | AAATGATCTGTGTGC[C/T]TCAGCCTCCCATAGT | 5663 |
rs758513966 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73196539 | TAGGCAGTGGCGCCA[A/T]CTTGGCTCACTGCAG | 5663 |
rs758527602 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222587 | CACTATGAAAAAATT[C/T]GTTCAGTGTTTTCTG | 5663 |
rs758529628 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209195 | CGGGACTTCTGCCCC[A/T]CCAACTCAGAAGGGG | 5663 |
rs758562722 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73198414 | GATTAGGGCAAGCTC[A/G]AGGATTCCTTTGAGT | 5663 |
rs758564824 | snp | A/G | 1.65919e-05 | 0.00288022 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73148043 | GTTACCTGCACCGTT[A/G]TCCTACTTCCAGAAT | 5663 |
rs758582084 | in-del | -/ATTT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73166997 | CAGACTGGGTGATTT[-/ATTT]ATTTATTTATTTATT | 5663 |
rs758759034 | snp | A/G | 1.65067e-05 | 0.00287282 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192908 | TCACAGGAATGCCCC[A/G]CTGGAGTGTTTTCTT | 5663 |
rs758786670 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73199506 | GATATTCAGTGGTGG[A/G]TATCCTCATTGATAG | 5663 |
rs758812568 | snp | A/G | | | intron-variant, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73138148 | CAGACTGGGAGAACC[A/G]CAAGGTGATTATCCC | 5663 |
rs758812787 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73151768 | GAAATGAGGTTTCAC[C/T]GTGTTGCACAGTCTG | 5663 |
rs758814165 | snp | A/G | 3.4915e-05 | 0.00417807 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73198062 | GTGTCCGAAAGGTCC[A/G]CTTCGTATGCTGGTT | 5663 |
rs758833776 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73218240 | TACATGTGTGCACCA[C/T]CATGCCTGGCTAATT | 5663 |
rs758879057 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73190486 | ACCTTGTCTCTATTT[-/A]AAAAAAAAAAAAAAA | 5663 |
rs758898832 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73139558 | GCACTCCAGACTGGG[C/T]TACAGAGCGAGACTC | 5663 |
rs759013690 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73162017 | AAAAAAAAAAAAAAA[-/T]AGAAAAAGAAACCAA | 5663 |
rs759031467 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73190114 | CCAGCAGTCCCTGCT[C/T]CTGCTTCTGAAGAAA | 5663 |
rs759076775 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73189538 | AGTGGCGTGAACCTG[A/G]GAGATGGAGGTTGCT | 5663 |
rs759101530 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73157128 | CTTGAGAAAGATACC[-/T]TTTTTTTTTTTTGCG | 5663 |
rs759114801 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73174336 | CCCACCAGTTTCAAG[C/T]GATTCTCCTGCCTCT | 5663 |
rs759120634 | snp | A/G | 9.88435e-05 | 0.00702937 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73219148 | GGGTTTGTGCCTTAC[A/G]TTATTACTCCTTGCC | 5663 |
rs759199292 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73157111 | AAGCACCTACACACT[C/T]CCTTGAGAAAGATAC | 5663 |
rs759284725 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73195021 | TCAGTTGTGGAACTA[C/T]AGAAGTCATATACTC | 5663 |
rs759306043 | snp | C/G | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136121 | TAACAGCATTCTCTT[C/G]ATTGTGATGCAGCTG | 5663 |
rs759384156 | snp | A/G | 1.64743e-05 | 0.00287 | missense | PSEN1 | GRCh38.p7 | 14:73217218 | GACTGGAACACAACC[A/G]TAGCCTGTTTCGTAG | 5663 |
rs759437122 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73196985 | TTGCCCAGGCTGGAG[C/T]GCAGTGGCGCAATCT | 5663 |
rs759453005 | snp | A/G | | | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137550 | GGAGAAGTCTAAGCT[A/G]AGGAAGGGGAAGAGG | 5663 |
rs759466597 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73197327 | CAGGCATGTTGTTTC[C/G]TCTCTGATTTATTAT | 5663 |
rs759482396 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73214328 | CTGAGATCAGGAGTT[C/T]GAGACCAGCCCAACC | 5663 |
rs759499223 | snp | A/G | 1.65891e-05 | 0.00287998 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73148037 | GACAGAGTTACCTGC[A/G]CCGTTGTCCTACTTC | 5663 |
rs759538127 | in-del | -/ACG | 0.00036345 | 0.0134756 | cds-indel | PSEN1 | GRCh38.p7 | 14:73170825 | AACGGCAGGAGCACA[-/ACG]ACAGACGGAGCCTTG | 5663 |
rs759550651 | in-del | -/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73172320 | ATGGTGTTCTGAAAG[-/C]CAAACTTTTAGCCTT | 5663 |
rs759584427 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73191574 | TTTTTTAGTTTTAGG[C/G]TCTTGCTGTGTTGCC | 5663 |
rs759600407 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73157207 | CTTGGCTCACTGCAA[C/T]GTCTGCCTCCTGGGT | 5663 |
rs759607383 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73203183 | TCCCAGGTTCAAGCG[A/T]TTCTCCTGCCTCGGC | 5663 |
rs759694931 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73145101 | CTTCACCATGTTGGC[C/T]AGGCTGGTCTCGAAC | 5663 |
rs759784749 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73146014 | CGGGGGGCTGAGACA[C/T]GAAAATTACTTAAAC | 5663 |
rs759820143 | snp | G/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222382 | GATGATGTTTATTAC[G/T]TGTTATTTACGTGGC | 5663 |
rs759834354 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73192571 | TAATGTTTGGGAGCC[A/G]TCACATTATTCTAAA | 5663 |
rs759858141 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73210670 | CTCCAAACCAGAGAA[G/T]ATTCAGGTTTTTGGA | 5663 |
rs759864136 | snp | A/G | | | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136795 | CGGCCGGGTGGAGAG[A/G]GATTCCGGGGAGCCT | 5663 |
rs759884745 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73179204 | TTGCCCCACTCTCTC[A/G]GGACTGACATTCTTC | 5663 |
rs759891729 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73177335 | TCAAATGAATTATCC[C/T]TCATACCATTTCATT | 5663 |
rs759979983 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73202896 | AAGTCTATTTAATAA[A/C]CACAGAATATGAGAC | 5663 |
rs760051592 | snp | C/G/T | 3.29464e-05 | 0.00405861 | missense | PSEN1 | GRCh38.p7 | 14:73211838 | GTGAGGAATGGGAAG[C/G/T]CCAGAGGGACAGTCA | 5663 |
rs760061527 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73178250 | TTTGAGACCGAGTCT[C/T]GCTTTGTCACCCAGG | 5663 |
rs760098851 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73166597 | TCAATTGCAGATATA[A/G]CATTCTTGGCAGATG | 5663 |
rs760125838 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73140023 | TAGTTGTATTCTGTC[C/T]ATTTCCTCAGAATTT | 5663 |
rs760139599 | snp | A/G | 3.29783e-05 | 0.00406055 | missense | PSEN1 | GRCh38.p7 | 14:73211921 | TCCAGCAGTATCCTC[A/G]CTGGTGAAGACCCAG | 5663 |
rs760141976 | snp | A/G | 1.64855e-05 | 0.00287097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186815 | CTTTTTAAGGGTTGT[A/G]GGACCTGTTAATTAT | 5663 |
rs760158803 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73217211 | CAGTGGAGACTGGAA[C/T]ACAACCATAGCCTGT | 5663 |
rs760163162 | in-del | -/AA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73193550 | GCGAGACTCTGTCTC[-/AA]AAAAAAAAAAAAAGC | 5663 |
rs760165585 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73200343 | GGCGCAATCTCAACT[C/T]ACTGCAACCTCCATC | 5663 |
rs760169591 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73142544 | AGTAACCATGTTCTG[C/T]AGGAGTTTGAGGTTT | 5663 |
rs760176852 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73141789 | AAACTACATCTTGGC[C/T]GGGTGCCGTGGCTCA | 5663 |
rs760217898 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73172997 | CCCTTACTTGTTCTC[A/G]TAGCCATCCTAAATA | 5663 |
rs760229806 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73153123 | AAAAAATAAATGAAA[C/T]GGGTGATCTAAATTT | 5663 |
rs760244944 | snp | A/G | 1.64751e-05 | 0.00287007 | intron-variant | PSEN1 | GRCh38.p7 | 14:73219112 | TATGTGTGAATGTGT[A/G]TCTTTCCCATCTTCT | 5663 |
rs760283723 | snp | A/G | 3.34778e-05 | 0.00409119 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211964 | GCATTTCTCTATGTT[A/G]CAAAGTCATGGATTC | 5663 |
rs760324444 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73199224 | AAAAGTTGATATTTG[-/T]AGATAGAGACTTGAA | 5663 |
rs760342305 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73160179 | CTTTTAGTGACTTGC[G/T]TATTTTGCTTAGCAT | 5663 |
rs760343722 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73181999 | GGCTGGTCTTGAACT[C/T]CTGACCTCAGGCAAT | 5663 |
rs760479085 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73207436 | AAATATTGGTGAGGA[A/T]AAAAAGGCCTTAATT | 5663 |
rs760499969 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73165304 | ACAGTATTTTTTTCC[G/T]TAAAGATGGTGTCTC | 5663 |
rs760525569 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73161644 | TTGTGCACACAGTGC[C/T]TAATTTTTCCAGCAA | 5663 |
rs760593463 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136486 | TGGGACAGGCAGCTC[C/T]GGGGTCCGCGGTTTC | 5663 |
rs760601237 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73148778 | TCTCTACTAACAATA[C/T]AAAAATTAGCCGGGC | 5663 |
rs760611656 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73147742 | TTGATTGGTTTAAAT[A/G]AATTTACTAGGATTT | 5663 |
rs760615714 | snp | C/T | 1.66402e-05 | 0.00288441 | utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73148017 | TTCTATACAGTTGCT[C/T]CAATGACAGAGTTAC | 5663 |
rs760627634 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73181151 | GTCATTTAAAAATCA[C/T]AGTTTCAGCTGGGCG | 5663 |
rs760648712 | snp | G/T | 8.97159e-05 | 0.00669701 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73198044 | AGATTTAGTGGCTGT[G/T]TTGTGTCCGAAAGGT | 5663 |
rs760656723 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73197212 | TGCTGGGATTGCAGG[C/T]GTGAGCCACTGCGCC | 5663 |
rs760690068 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73149302 | TGAGTCCAGCATGGG[C/G]AACATAGAGAGGTTC | 5663 |
rs760715744 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73201624 | GGTGAAGAAGGAGAG[A/G]TATAGTAAATGTCAT | 5663 |
rs760760368 | snp | C/T | 1.648e-05 | 0.0028705 | missense | PSEN1 | GRCh38.p7 | 14:73171008 | TGGTCGTGGCTACCA[C/T]TAAGTCAGTCAGCTT | 5663 |
rs760766616 | in-del | -/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73145345 | ATTATTTTATTATTT[-/G]TTTTTTTGAGACAGG | 5663 |
rs760776475 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73174648 | GGTCCCTATAAAATA[C/T]GGTATAACTAAAATC | 5663 |
rs760815228 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73169537 | AGCCTGTTTATCTTA[C/T]TGTGTTCCATTGTGT | 5663 |
rs760833733 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73155703 | TTCACTTTTTTTGTA[G/T]AGCTGGGGTCTCGTT | 5663 |
rs760886723 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73151567 | AATAATTTAAAAAGC[C/T]ATTTTGAAAAAGTAA | 5663 |
rs760972818 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73159419 | CCTACTTCAAGTTCT[C/G]AGGAGTTTTTTCCTG | 5663 |
rs760987526 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73202895 | CAAGTCTATTTAATA[A/G]CCACAGAATATGAGA | 5663 |
rs760999979 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73145019 | TGCCTCAGCCTCCTT[A/T]GTAGCTGGGATTACA | 5663 |
rs761010563 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73211824 | TGATGGCGGGTTCAG[C/T]GAGGAATGGGAAGCC | 5663 |
rs761036625 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73161075 | CGCCTCCCAGGCTCA[A/G]GCAGTCCTTCCACCT | 5663 |
rs761061377 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73163737 | GGCATTCCAGATGAA[C/G]CAGCCCTGAGCGGGG | 5663 |
rs761079214 | snp | A/C | 1.66255e-05 | 0.00288314 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211723 | TTTCTTAAAGGTATT[A/C]AATTTTTCTAAATAT | 5663 |
rs761091686 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220938 | GTTTATGAGAAACTT[A/G]GTTTCCTCCTGTGGC | 5663 |
rs761108253 | in-del | -/CT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73162449 | GCTCGCTCGCGCGCT[-/CT]CTCTCTCTCTCTCTC | 5663 |
rs761186483 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73175949 | CCCCACCAGTGCTGA[A/G]TTTCTTTTTTAAAAC | 5663 |
rs761186752 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73192390 | AGACTGCAGTGAGCC[A/G]TGATTGCACCACTTT | 5663 |
rs761195349 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209604 | GTCTATTTGGAGAGA[G/T]AGATGGTCAACAAAT | 5663 |
rs761235726 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73177222 | TTTCATCCTTAAATA[A/T]AACTTTTAATGTAGT | 5663 |
rs761329407 | in-del | -/GT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73191399 | TATGTGTATGTATAA[-/GT]GTGTGTGTGTGTATG | 5663 |
rs761357795 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73206007 | GCATCTTTTGAATTA[A/T]AATCACCATCTGAGG | 5663 |
rs761369156 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73198951 | GCTAATTTTTTTGTG[C/T]TGTGTGTAGAGACTG | 5663 |
rs761376196 | snp | A/G | 1.68661e-05 | 0.00290392 | utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73147997 | TGTTTTCTGTGAAAC[A/G]GTATTTCTATACAGT | 5663 |
rs761395518 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73139336 | TAATCTGCCAGCACT[G/T]TGGGAGGCCGAGGCA | 5663 |
rs761410242 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73195851 | ATCCTATGAAGTATC[A/G]AGGCAGTTATTATCC | 5663 |
rs761450049 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73151386 | TATATGGATCTTAGA[A/G]CTATTTTAGAGATTG | 5663 |
rs761496722 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73192797 | TAGTGCCCTCATGGC[C/T]CTGGTGTTTATCAAG | 5663 |
rs761574956 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73216397 | TACAGCTCTATTAAT[C/T]TTCCACAATCATTGA | 5663 |
rs761670085 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73172772 | GAGGTAGGCAGTCCA[A/G]ATTAGTACGGTGGCT | 5663 |
rs761684988 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73207252 | CACAAGTTAGAAGTT[A/G]TTATTAGATGGAGTT | 5663 |
rs761701837 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73159329 | TAGGACTACAGATGT[A/G]TGCCACTGCACCCAG | 5663 |
rs761708452 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73144033 | TTTGCATTATAGCTT[-/A]TCTTTTTTTTTTTTT | 5663 |
rs761714829 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73206149 | ACTAAAAATGATGAA[C/G]AGTTTTGTGATAGCA | 5663 |
rs761740204 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194752 | TTTTTGTATTTGTAG[G/T]AGAGACGGGGTTTCA | 5663 |
rs761787391 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73146358 | TGCACCCAGCTAATT[A/G]TTTTTTTGTAGAGAT | 5663 |
rs761876896 | snp | G/T | 0.000188733 | 0.0097124 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208942 | TCAGCCCCTCCTCAG[G/T]CTCCCTCCCATGCTT | 5663 |
rs761877415 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73147565 | CCCTTTGCTGGAAAT[C/T]AGAAGTCATTAAGTA | 5663 |
rs761912772 | in-del | -/TATCTAATC | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73200656 | TATCATCTCTAATCT[-/TATCTAATC]TAATGCCTTATCAAG | 5663 |
rs761943550 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73180697 | AGAGAAGATACTGTT[A/G]TGTACTATAAAACAG | 5663 |
rs762025703 | snp | C/T | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135558 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 5663 |
rs762114375 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73186803 | AAAAAATCTGTACTT[C/T]TTAAGGGTTGTGGGA | 5663 |
rs762121676 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73169196 | TAACACCTCTGATTT[C/G]TGCTCCACTTTTGGC | 5663 |
rs762141719 | in-del | -/T | 1.6473e-05 | 0.00286988 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171059 | AGCTGTACGTATGAG[-/T]TTTGTTTTATTATTC | 5663 |
rs762146589 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73155474 | ATGAGGTATATTTAT[A/G]TGTCTAGCATAGAAT | 5663 |
rs762151664 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73200631 | CAGATAAAAATAAAT[C/T]TCACGGTAACTATCA | 5663 |
rs762193829 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73174426 | TTTAGTAGAGACAGG[A/G]TTTCACCATGTTGAC | 5663 |
rs762317859 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73220709 | GTGGTCTCTGCCCGC[A/G]TTACCTTTCCTCTCA | 5663 |
rs762374300 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73191181 | TATAAGATTATAAAG[A/G]AGAAAAATGACCAGA | 5663 |
rs762387542 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73159822 | AACATGGACTACTTG[A/G]GTTTTTTTCTTTTTT | 5663 |
rs762407109 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73158728 | TGGCTTCCCAAAGTG[C/T]TGGGATTATAGGCAT | 5663 |
rs762410961 | in-del | -/CT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73143425 | CTGGCATTGTTTACA[-/CT]CTCTCTGTAACTCTG | 5663 |
rs762414700 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209504 | TTTCATTCATTTTAC[A/T]GATGTTGACTGAGCA | 5663 |
rs762468297 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73175405 | GGCTGGGATTACAGG[C/T]GTGAGCCACCATACC | 5663 |
rs762475015 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73175858 | TTATAACTGTCTTGG[G/T]ATTCAAAATCTCGTT | 5663 |
rs762499499 | in-del | -/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73142158 | GTTACATTTACTATT[-/G]GATGTGATCCTTTAA | 5663 |
rs762541377 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73197506 | ACTTCTCAGTAGTAC[A/G]TAATACTGCTTTTAA | 5663 |
rs762575275 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73196279 | GCAGAATCAAACAAG[C/T]TGAAAATCTCATCAC | 5663 |
rs762602739 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73203884 | CTGCATATTTTCCAG[A/C]CAGGCATGACTATAA | 5663 |
rs762627641 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73151310 | GTGCTGCAGTGACAT[A/G]CTAATTCATTAGTCT | 5663 |
rs762700122 | snp | G/T | 1.64966e-05 | 0.00287194 | missense | PSEN1 | GRCh38.p7 | 14:73192648 | TTTTTTTTCAGGGAA[G/T]TGTTTAAAACCTATA | 5663 |
rs762780217 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73212866 | CCAAGTTATTTTTGG[C/T]TGTCTTGTTTTTGCA | 5663 |
rs762843550 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73216303 | TTAACTGTAAACGGG[C/T]ACAAGGTACCTGACT | 5663 |
rs762900904 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73158616 | CGTGAGCCATCACAC[C/T]TGGCCAGTTTTTATT | 5663 |
rs762907738 | snp | C/G | | | missense | PSEN1 | GRCh38.p7 | 14:73170922 | TGAGGAAGAAGATGA[C/G]GAGCTGACATTGAAA | 5663 |
rs762957128 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73192871 | CAGTATATGGTAAAA[C/T]CCAAGACTGATAATT | 5663 |
rs762959076 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73205867 | AGGGGCACAGAGGAG[G/T]CCTCTTGACTATCCC | 5663 |
rs762961061 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73171906 | TGTTTCTCCTAACAC[A/G]ATTAAGTCCTTCTTG | 5663 |
rs763001979 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73146125 | TAAAGACAGGAACAA[A/C]GGTATCGATAACTCT | 5663 |
rs763004238 | in-del | -/AAAAT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73166077 | AATAATAATAAAATA[-/AAAAT]AAAAGTAGTATCCAG | 5663 |
rs763006524 | in-del | -/TG | 1.64754e-05 | 0.00287009 | intron-variant | PSEN1 | GRCh38.p7 | 14:73219106 | ATAATTATGTGTGAA[-/TG]TGTGTGTCTTTCCCA | 5663 |
rs763024617 | in-del | -/AC | 1.64925e-05 | 0.00287158 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173719 | TAAGGTGAGCATGAG[-/AC]ACAGATCTTTGCTTT | 5663 |
rs763028645 | snp | C/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223300 | TAGTGGATGTGCTGG[C/G]TCCACCCTGAGCCCT | 5663 |
rs763051015 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73168835 | GGCACCTGGCCATCC[C/G]CGAATGGCCGCGTTG | 5663 |
rs763077064 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73177107 | CTTTGGTCCTTTTTG[C/T]AGTTTTCTAAAGCTA | 5663 |
rs763091433 | snp | A/G | 0.000175516 | 0.00936627 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208885 | CATGGCACCCAGGCT[A/G]TTCATGCCAAAGGGT | 5663 |
rs763180479 | snp | C/T | 1.68849e-05 | 0.00290554 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73206453 | GAGAGTATCCAAAAA[C/T]TCCAAGTATAATGCA | 5663 |
rs763204855 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73179310 | GAGGACTGGGCATAC[A/G]AGAATGGAGAAAAGC | 5663 |
rs763206634 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73200042 | GTGAGCCACCATGCC[C/T]GGCCACTGCTTTGTT | 5663 |
rs763232042 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73168394 | AAGATTTCAGCAGCT[G/T]GGAGAACAATATAAG | 5663 |
rs763279216 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73200433 | TGCCACCACGCCTGG[A/C]TGATTTTTGTATTTT | 5663 |
rs763328798 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73166877 | GAAGAGAAATCCTGA[C/T]CTCCAGACTGAAGGA | 5663 |
rs763332706 | in-del | AGATTTGCATTATAGCTTATCTTTTT/TTTTCATTTAACC | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73144015 | AAAAAAAAAAAAAAA[lengthTooLong]TTTTTTTTTTTTTTT | 5663 |
rs763399179 | in-del | -/AA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73200850 | GAGGTCAGGAGTTTG[-/AA]ACCAGCCTGGCCAAC | 5663 |
rs763403691 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73212384 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACTG | 5663 |
rs763404921 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73188770 | GGAGGTTTTCTTTTC[C/T]TTCTTTTGTTTGTTT | 5663 |
rs763426257 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73142067 | GGGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAGA | 5663 |
rs763453503 | snp | G/T | 1.64743e-05 | 0.00287 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73217175 | CTACAGTGTTCTGGT[G/T]GGTAAAGCCTCAGCA | 5663 |
rs763478394 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73196399 | TACTATATTATATTA[C/T]AGTTCTATATATACT | 5663 |
rs763479305 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73153440 | TTGGCATTAGAGGAA[C/T]GGTTAAACCTCTGAC | 5663 |
rs763497864 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73140833 | TAAAAACAAGTTGCT[A/G]TAGTAACTCTACATT | 5663 |
rs763505170 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73163666 | ATTCGATAGTCAGGA[A/G]ATTCTCTCTCTACCA | 5663 |
rs763528319 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73149045 | ATTTTTAGAGGTGGA[C/T]CCAGAATAGAGGAAA | 5663 |
rs763560607 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209554 | CTGGGGATATAGCAC[C/T]GAACAAGATTTCCCC | 5663 |
rs763561530 | in-del | -/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73207963 | TACAGGCCACTACCA[-/C]TAGTAAACCTGATAG | 5663 |
rs763587458 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73142217 | TTCATAACATTAGAA[G/T]TTGGGCCGCCTGTCC | 5663 |
rs763602334 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73182254 | TATGGCTGAGACCAG[A/G]GGATCACTTGAAGCC | 5663 |
rs763638380 | snp | A/C | 3.29603e-05 | 0.00405944 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211749 | AATATTAGAGCTGTA[A/C]CTTCCACTTTCTCTT | 5663 |
rs763772976 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73161548 | TGATATGGATTAAAT[G/T]TAGCAACAGAAAAAG | 5663 |
rs763831389 | snp | A/G | 3.29462e-05 | 0.00405857 | missense | PSEN1 | GRCh38.p7 | 14:73192754 | GGAAAGGTCCACTTC[A/G]ACTCCAGCAGGCATA | 5663 |
rs763853152 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73214734 | GTATGATTCCACTTA[A/C]ATCAGAGTAGTCAGA | 5663 |
rs763882941 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73205043 | TTGGTTGACCTCAGA[A/T]ATAACAAGGTGGTCG | 5663 |
rs763977353 | in-del | -/AA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73158075 | ATGTGGTTCCTTTTT[-/AA]ATTGCTGAGTTGTAT | 5663 |
rs763991845 | in-del | -/T | 9.95107e-05 | 0.00705305 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192633 | TTAAAATCTGTGTAA[-/T]TTTTTTTCAGGGAAG | 5663 |
rs764012315 | in-del | -/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73179950 | CTTAATATATTTTTT[-/G]TCGCATTTGTACATC | 5663 |
rs764013084 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73157450 | AGCCCAAGAAAGATA[C/T]ATTTTTAAAAACAGC | 5663 |
rs764054413 | snp | A/G | 1.79168e-05 | 0.00299301 | intron-variant | PSEN1 | GRCh38.p7 | 14:73170747 | TCTAACCGTTACCTT[A/G]ATTCTGCTGAGAATC | 5663 |
rs764087851 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73192897 | TAATTTGTTTGTCAC[A/C]GGAATGCCCCACTGG | 5663 |
rs764117621 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73212925 | CAAGAATATTAAGTA[A/G]TTTTAAGGAAACAAA | 5663 |
rs764128019 | snp | C/G | 1.64743e-05 | 0.00287 | missense | PSEN1 | GRCh38.p7 | 14:73219215 | ATCACCTTTGGGCTT[C/G]TTTTCTACTTTGCCA | 5663 |
rs764133235 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73193848 | TTTTTGTAGAGAGAA[C/T]GTCTTGCTATATTGC | 5663 |
rs764139115 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73177884 | TGAGCTTTTTGAATC[C/T]CTAGGTTTATGTCTT | 5663 |
rs764179760 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73171556 | GCGCACATTTGGACA[A/G]GGGAGGGGAAAGGGT | 5663 |
rs764232011 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73146288 | TAATTCCTGGACTCA[A/G]GCCATCCCCCCACCT | 5663 |
rs764234798 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73166998 | CAGACTGGGTGATTT[A/C]TTTATTTATTTATTT | 5663 |
rs764257984 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73179387 | TTTGGGAGGCCAAGG[C/T]GGGCAGATTGCCTGA | 5663 |
rs764283892 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73199575 | GCACTTACAGAGTGC[A/G]TCCATGAACTTATGA | 5663 |
rs764290885 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223381 | ACGATTTCCCAGAAA[A/G]CAATTTTCCTTTTGA | 5663 |
rs764300161 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73153458 | TTAAACCTCTGACTC[C/G]AGGGAATCACAAAGC | 5663 |
rs764368535 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73143541 | AAATGGAAGAATAGA[A/T]GTGAAAAGAACTTTG | 5663 |
rs764451732 | snp | C/T | 3.46242e-05 | 0.00416064 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206337 | TTGTTGTTGTCTATG[C/T]ATACTTTGTGTGTCC | 5663 |
rs764516732 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73190288 | AGCCCAGGGGTTCTA[A/G]ACCATCCTGGGCAAC | 5663 |
rs764538573 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73152113 | AGGCGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 5663 |
rs764542252 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73181945 | CGCCTAGCTAATGTT[C/G]GTATTTTTAGTAGAG | 5663 |
rs764563967 | snp | G/T | 1.64882e-05 | 0.00287121 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186808 | ATCTGTACTTTTTAA[G/T]GGTTGTGGGACCTGT | 5663 |
rs764616438 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73189029 | CTCTTGACCTCAGGT[G/T]ATCCACCTGCCTCCG | 5663 |
rs764686202 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73207797 | CCTGCCAAAGGCAAG[A/C]CAGGCATGGAGCAGC | 5663 |
rs764715036 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73160394 | GTTTGTAATTCAGTT[C/T]GTTTTTATATATACT | 5663 |
rs764907374 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73159444 | TTCCTGCATTTTCTT[C/T]TGGAAGCTTTATAGT | 5663 |
rs764915777 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73189569 | GTGAGCCGAGATCGC[A/G]CCATTGCACTCCCAC | 5663 |
rs764926435 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73195031 | AACTATAGAAGTCAT[A/G]TACTCTCTCTGACTT | 5663 |
rs764930114 | snp | A/G | 1.66305e-05 | 0.00288357 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192620 | TATTGTACATCTTTT[A/G]AAATCTGTGTAATTT | 5663 |
rs764956038 | snp | A/G | | | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137558 | CTAAGCTAAGGAAGG[A/G]GAAGAGGAGGCCAAG | 5663 |
rs764971634 | snp | A/G | 1.64743e-05 | 0.00287 | missense | PSEN1 | GRCh38.p7 | 14:73219194 | TTGCCAGCTCTTCCA[A/G]TCTCCATCACCTTTG | 5663 |
rs765021336 | snp | A/G | 3.29592e-05 | 0.00405938 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186835 | CTGTTAATTATATTG[A/G]AATGCTTTCTTTTCT | 5663 |
rs765039431 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73213731 | CAAGAAAATGTAAAA[A/G]TGATCTGTAAACACA | 5663 |
rs765046445 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73169627 | CAAGTTTGCTAAAAA[C/T]GAAACATCTGATTGT | 5663 |
rs765053487 | snp | A/G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73181303 | AAAAATTAGCTGGGC[A/G/T]TGGTGGCGAGTGCCT | 5663 |
rs765069538 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73172508 | CAAAGGTGTAATAAC[-/A]AAAGTTATTCACAAA | 5663 |
rs765079294 | snp | A/G | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136149 | CTGGTTCGCAAATAG[A/G]TACCCTAAAGAAATG | 5663 |
rs765102624 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73181946 | GCCTAGCTAATGTTC[G/T]TATTTTTAGTAGAGA | 5663 |
rs765167125 | snp | C/T | 0.000145402 | 0.00852524 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160025 | GACGAGTTCTCGCCA[C/T]ATTGGCCAGGCTGAT | 5663 |
rs765219293 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73203186 | CAGGTTCAAGCGATT[C/G]TCCTGCCTCGGCCTC | 5663 |
rs765247843 | in-del | -/TT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73158276 | AGGTGTATATTTAAC[-/TT]TTTTTTCTATCTATC | 5663 |
rs765294054 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73157208 | TTGGCTCACTGCAAC[A/G]TCTGCCTCCTGGGTT | 5663 |
rs765328424 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73192604 | ATGTTTTGGTGAAAA[G/T]TATTGTACATCTTTT | 5663 |
rs765330647 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73191763 | GTGTTGCCCAGGCTC[G/T]TCTGGAATTCCTGGC | 5663 |
rs765338998 | in-del | -/ATATATATATATATATATA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73202420 | TATCTATCACATACT[-/ATATATATATATATATATA]TATATATATATATAT | 5663 |
rs765383344 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73177430 | TTGTTTTGAGATAAA[A/G]TCTTGCTTTGTCACC | 5663 |
rs765462902 | in-del | -/T | 1.64735e-05 | 0.00286993 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173551 | CCTAGGGCTTTTGTG[-/T]TTGTTTTATTGTAGA | 5663 |
rs765502166 | in-del | -/AT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73164865 | TTCTTTTATTTTCAT[-/AT]ATATATATATGTTCA | 5663 |
rs765670175 | snp | A/T | 3.29451e-05 | 0.00405851 | missense | PSEN1 | GRCh38.p7 | 14:73173646 | ATGCTGCCATCATGA[A/T]CAGTGTCATTGTTGT | 5663 |
rs765739473 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73166688 | GTATGTTCTGGTCCC[A/G]TTGGCCTCACCTTCC | 5663 |
rs765750017 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73160969 | AGATATATGATTTGC[-/T]TTTTTTTTTTTTTTT | 5663 |
rs765802323 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73187652 | AGGTACAGAAAGTTA[C/G]TGAAGAAGTTTCCAC | 5663 |
rs765838715 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73217948 | GCCTGCCACCACGCC[C/T]GGCTAATTTTTGTAT | 5663 |
rs765853639 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73188465 | TGGATACCAACCTGC[A/G]CAACATAACAAGACT | 5663 |
rs765890474 | snp | C/G | 1.6504e-05 | 0.00287258 | missense | PSEN1 | GRCh38.p7 | 14:73211930 | ATCCTCGCTGGTGAA[C/G]ACCCAGAGGAAAGTA | 5663 |
rs765891278 | snp | C/G | 1.64836e-05 | 0.0028708 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186817 | TTTTAAGGGTTGTGG[C/G]ACCTGTTAATTATAT | 5663 |
rs765969198 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73182078 | TGTGCCTGGCCTGAA[A/G]GGGAAATGTTGGTAT | 5663 |
rs765979077 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73173061 | GAATATTGGCACCTG[A/G]AATAAAAATGTTTTT | 5663 |
rs766060557 | snp | C/G | 1.64743e-05 | 0.00287 | missense | PSEN1 | GRCh38.p7 | 14:73217216 | GAGACTGGAACACAA[C/G]CATAGCCTGTTTCGT | 5663 |
rs766071159 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73206314 | GATTTGTGTGGAGAA[A/G]TGATGGCTTGTTGTT | 5663 |
rs766076313 | in-del | -/TG | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73210147 | AACAAACAAAAGAAC[-/TG]AGAGATTACCTGATG | 5663 |
rs766108467 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73148825 | GTAATCCCAGCTACT[C/T]AGGAGGCTGAGCCAG | 5663 |
rs766164212 | in-del | -/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73184698 | GGGGCGGGGGGCTGA[-/C]CCCCCCACCTCCCTC | 5663 |
rs766180385 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73181159 | AAAATCATAGTTTCA[C/G]CTGGGCGTGGTGGCT | 5663 |
rs766185838 | snp | A/G | 1.67461e-05 | 0.00289357 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211966 | ATTTCTCTATGTTGC[A/G]AAGTCATGGATTCCT | 5663 |
rs766199156 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194140 | GGCAGCTTTCAGGTA[C/T]GTACTCTGTGGCTGT | 5663 |
rs766248021 | snp | A/G | 1.66228e-05 | 0.0028829 | missense | PSEN1 | GRCh38.p7 | 14:73148020 | TATACAGTTGCTCCA[A/G]TGACAGAGTTACCTG | 5663 |
rs766295174 | snp | C/G | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134601 | GGCGCAATCTCGGTT[C/G]ACTGCAACCTCTGCC | 5663 |
rs766384019 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73154570 | CATGCCACTGCACTT[C/T]AACCTGGGCAGCAAA | 5663 |
rs766389888 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73165579 | GGATAAGACTCCATC[C/T]CTACTAAAAATACAA | 5663 |
rs766432705 | in-del | -/CAGCCT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73218594 | ATTTTTTAAACACTG[-/CAGCCT]CAGCCTCATCATGCT | 5663 |
rs766458748 | snp | C/G | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135913 | AAGAGCAGGCAGATG[C/G]AAAAATCAAGTGACC | 5663 |
rs766482390 | snp | C/T | 2.29713e-05 | 0.00338897 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198150 | TATTTGAGAAGGATA[C/T]TGAATTAGTAATCAG | 5663 |
rs766630576 | snp | C/T | 3.29859e-05 | 0.00406102 | missense | PSEN1 | GRCh38.p7 | 14:73170872 | TTATCTAATGGACGA[C/T]CCCAGGGTAACTCCC | 5663 |
rs766633762 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73143502 | AGTACAGATTCCTTT[C/G]CTCATGAGGTTTCTT | 5663 |
rs766649827 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194463 | ATGAGATCTCACTGT[A/G]TTTCCCAGGCTTGTC | 5663 |
rs766798700 | snp | A/G | 1.64803e-05 | 0.00287052 | missense | PSEN1 | GRCh38.p7 | 14:73171010 | GTCGTGGCTACCATT[A/G]AGTCAGTCAGCTTTT | 5663 |
rs766802547 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73163769 | ACTAGAAGGCCAGTT[G/T]GAGAAAAGGAATGGA | 5663 |
rs766815842 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209681 | ACGTATAAGTTGCTA[C/T]GAAAGTTTATAATAG | 5663 |
rs766834989 | snp | A/G | 1.64735e-05 | 0.00286993 | missense | PSEN1 | GRCh38.p7 | 14:73211826 | ATGGCGGGTTCAGTG[A/G]GGAATGGGAAGCCCA | 5663 |
rs766846755 | in-del | -/CTT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73182888 | AAATAAGAACATCTC[-/CTT]CTTCCTTTGCCAAAA | 5663 |
rs766866661 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73151389 | ATGGATCTTAGAACT[A/G]TTTTAGAGATTGCTA | 5663 |
rs766886713 | in-del | -/TAA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73180600 | AACAGGAAAGGCAGT[-/TAA]TTATTATACATAATT | 5663 |
rs766901431 | in-del | -/TTTTTTTTTTT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73144036 | GCATTATAGCTTATC[-/TTTTTTTTTTT]TTTTTTTTTTTTGAG | 5663 |
rs766911262 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73186336 | GTGAGCCGAGATTGC[A/G]CCATTGCACTCCATT | 5663 |
rs766938313 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73197967 | GTTAATTCCTCCCTA[C/T]CACCCATTTACAAGT | 5663 |
rs766944659 | snp | A/G | | | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137850 | GCACTTTGGGAGGCC[A/G]CGGGGCGGATCCTTG | 5663 |
rs766954548 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73139353 | GGGAGGCCGAGGCAG[A/G]TAGATCACCTGAGGT | 5663 |
rs766955269 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73177312 | TCAGATACCTGGTAG[C/T]ATATAAATCAAATGA | 5663 |
rs766991666 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73199072 | GAGCTACCACGCCTG[A/G]CCATGTTTTCTTGTG | 5663 |
rs766998814 | snp | A/G | 1.6676e-05 | 0.00288751 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211959 | TATGTGCATTTCTCT[A/G]TGTTGCAAAGTCATG | 5663 |
rs767032985 | snp | C/G | 1.64939e-05 | 0.0028717 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211743 | TTTCTAAATATTAGA[C/G]CTGTAACTTCCACTT | 5663 |
rs767034217 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73171166 | GCTGGAGAGCCCATC[C/T]TCTGTGATGGTCAGG | 5663 |
rs767054124 | snp | A/C/T | 3.29491e-05 | 0.00405877 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73173671 | TGTTGTCATGACTAT[A/C/T]CTCCTGGTGGTTCTG | 5663 |
rs767122506 | in-del | -/GAAA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73191441 | TCCCGCTTTGAAGGT[-/GAAA]GAAAGCACACCTTTA | 5663 |
rs767131587 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73207194 | CTTAGGATAAGAGAG[-/T]TGAAAGGCCCTCTAA | 5663 |
rs767146336 | snp | A/T | 1.64738e-05 | 0.00286995 | missense | PSEN1 | GRCh38.p7 | 14:73211854 | CCAGAGGGACAGTCA[A/T]CTAGGGCCTCATCGC | 5663 |
rs767156303 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73187220 | ATGTTTTAAGAAAGG[A/G]TTTTAAGAATGTATA | 5663 |
rs767183297 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73206172 | TGATAGCAGGTGCAG[A/T]TTGAGTACTACAGTA | 5663 |
rs767210641 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73179360 | GGTGGCTCACGCCTG[C/T]AATCCTAACACTTTG | 5663 |
rs767214001 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73190225 | GGTGTGGTGGCTCAC[-/A]ACTTGTAATCTCACC | 5663 |
rs767216787 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73216404 | CTATTAATTTTCCAC[A/G]ATCATTGAATCATGT | 5663 |
rs767235902 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73140593 | TGATTTAAAACTATT[C/G]ATTTGTTTCACTATA | 5663 |
rs767254296 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73205067 | GTGGTCGTTCAGCTT[C/T]TTTGATTGTGTGTTT | 5663 |
rs767304099 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73193998 | GGTTACCTACTTTTT[A/G]TAAGGTAATGTATAG | 5663 |
rs767384146 | in-del | -/TTC | 8.26241e-05 | 0.00642692 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173744 | TTGCTTTCCACCCTG[-/TTC]TTCTTATGGTTGGGT | 5663 |
rs767412975 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73159351 | TGCACCCAGCTAATT[C/T]CGTTTGTATTTCATT | 5663 |
rs767417421 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73216188 | AGTAAAATAGGCGAG[A/G]CATGTATTGTATGAG | 5663 |
rs767446120 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73146432 | CCTGGCCTTAAGCTC[G/T]TTATTTTTTAAGCAA | 5663 |
rs767447252 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73179669 | TGGGTGTTAGGAGAC[C/G]TCTTTCCTGATCCTC | 5663 |
rs767448600 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73161926 | TTGGGAGGCTGAGGC[A/G]GGCGGATCACCTGAG | 5663 |
rs767464461 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73160139 | GGCTAGATATTTCAT[A/G]TAAGTGGAATCATAC | 5663 |
rs767531472 | in-del | -/GAGACAGAGTC | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73212130 | TTTTTTTTTTTTTTT[-/GAGACAGAGTC]TCGCTCTGTCGCCAG | 5663 |
rs767568126 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167281 | AGTATCCCTGATTTG[A/G]AAGTCTGAAATTCAA | 5663 |
rs767609242 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73147600 | TGTGGTTGAAAATGT[C/T]TGGTGTCTCAGGCGG | 5663 |
rs767621281 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73168523 | GCAGCGAGCAGAGAA[A/T]CAGGTGAGCGTTGGA | 5663 |
rs767625974 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | PSEN1 | GRCh38.p7 | 14:73192805 | TCATGGCCCTGGTGT[C/T]TATCAAGTACCTCCC | 5663 |
rs767684177 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73154319 | ACTTAATTGCAGAGC[C/T]AGGTGTGGTGGCTCA | 5663 |
rs767718789 | snp | A/G | 3.76102e-05 | 0.00433632 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206494 | AACTTTTATTAGATA[A/G]TATCTTGATTTTTCA | 5663 |
rs767775901 | in-del | -/TCTA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73158286 | TAACTTTTTTTTCTA[-/TCTA]TCTATCTATCTATCT | 5663 |
rs767871228 | snp | G/T | 1.69407e-05 | 0.00291034 | intron-variant | PSEN1 | GRCh38.p7 | 14:73170787 | GAAAATGTTTTTCTT[G/T]TGCTTATAGAATGAC | 5663 |
rs767914657 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73189222 | ACCAATATTTGGAGA[C/T]AAAATGATTGTTTAC | 5663 |
rs767919571 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73175883 | CTCGTTTTCAAAAAG[C/T]TTATATCAATTTGTA | 5663 |
rs767923360 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73155529 | TTTTTTTTGAGACAG[G/T]GTCTCCTTCTATCAC | 5663 |
rs767946544 | in-del | -/TACT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73200672 | TAATGCCTTATCAAG[-/TACT]TACCCCTGTTGTCAG | 5663 |
rs768027634 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73174508 | CAAAGTGCTGGGATT[A/G]CAGGCATGAGCCACT | 5663 |
rs768069021 | snp | C/T | 1.72047e-05 | 0.00293293 | utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73147970 | TTCCCTTTTCAGAAC[C/T]TCAAGAGGCTTTGTT | 5663 |
rs768075288 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73208979 | ACCCAAAGTCCAGAG[A/G]GGGCCAAGGTGGCAG | 5663 |
rs768080539 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73162429 | CATGCTCTCGTTCTC[C/T]CTCTCGCTCGCTCGC | 5663 |
rs768097566 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73178914 | GCCACCCAGTCACCA[A/G]TCTGGGACTGGTATA | 5663 |
rs768105824 | in-del | -/ATTA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73142597 | GAGAGAAGAAAACGT[-/ATTA]ATTCTTTTCTGTTGG | 5663 |
rs768195092 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73145774 | ACTGTCATCAGGGAC[C/T]GTCTGTATTGTGAAA | 5663 |
rs768205004 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73177069 | CCACTTGACACTGAT[G/T]CTGGCTTTTGCTTTT | 5663 |
rs768220257 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73166232 | TAAACCAGATCATCC[A/G]GTTGGGGACTCTGAA | 5663 |
rs768247019 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73164545 | TTACAACAACCCTAT[C/G]AGGAGATACTTTTTT | 5663 |
rs768251331 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73210523 | TACTTATAATTAATT[A/G]TGGAGGTAAATACCA | 5663 |
rs768275156 | in-del | -/TT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73191295 | GCATAAATGGGATCA[-/TT]TAAATGGGATCCTAT | 5663 |
rs768304317 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73211471 | ACCCCACAACCTTAG[A/G]GCTTTTGTTAGGAAG | 5663 |
rs768337488 | in-del | -/TG | | | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73224139 | TATGTCAGAAGAAAC[-/TG]TAAACTTATAAGACG | 5663 |
rs768409524 | snp | A/T | 2.2188e-05 | 0.00333069 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198005 | ATACATTTTATTAGA[A/T]GTCTTTTATGTTTTT | 5663 |
rs768433317 | snp | A/G | 1.70994e-05 | 0.00292394 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171083 | ATTATTCTCAAAGCC[A/G]GTGTGGCTTTTCTTT | 5663 |
rs768453759 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73204279 | CTGGGATTACAGGTG[G/T]GAGCCACCATGCCTG | 5663 |
rs768482010 | in-del | -/T/TT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167742 | AAATAACGTTTTCTG[-/T/TT]TTTTTTTTTTTGTCT | 5663 |
rs768483219 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73200215 | GTTTCTTAGTTACAG[A/G]TCTGAATTTATTTTG | 5663 |
rs768509574 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73173938 | GAGGATCACTTGGGC[C/T]CAGGAGTTCACAAGC | 5663 |
rs768521549 | snp | A/C | 3.29614e-05 | 0.00405951 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73170964 | GCATGTGATCATGCT[A/C]TTTGTCCCTGTGACT | 5663 |
rs768536282 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73188340 | TTTGATAAGATTCCT[C/G]TTCTTGATCAGATTC | 5663 |
rs768538003 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73141369 | CTTGCTCTTTTTAGC[A/G]TCTGCTGCTTTCACA | 5663 |
rs768542962 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73176890 | ATTACGTAAGATTCC[G/T]CTCAAATTCAGTCCT | 5663 |
rs768634772 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73147359 | TCTCTGGATTCCCTT[C/G]TCCTTTTGTAAAATA | 5663 |
rs768639296 | in-del | -/A | | | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73138069 | GAGTGAGACTGTCTC[-/A]AAAAAAAAAAAAAAC | 5663 |
rs768667211 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73198428 | AAGGATTCCTTTGAG[-/T]TGACTGGTTTAGATG | 5663 |
rs768701900 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73206036 | GGCTTTTGTGAGCTC[A/C]AGTTTGTCCTGGAAT | 5663 |
rs768730001 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | PSEN1 | GRCh38.p7 | 14:73211796 | AGTCACAAGACACTG[C/T]TGCAGAGAATGATGA | 5663 |
rs768733489 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73172605 | TCACACTACAGTAGC[A/G]CAGTTGAGTGTTTGC | 5663 |
rs768786711 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73160013 | TTTTTTTGTAGAGAC[A/G]AGTTCTCGCCATATT | 5663 |
rs768786722 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73173849 | AGTTTTCTTCCTCCT[C/T]ACTGTGGAACATTCA | 5663 |
rs768822103 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194726 | GGCATCTGCCACCAC[A/G]CCCGGCTATTTTTTT | 5663 |
rs768878052 | in-del | -/A | 1.64742e-05 | 0.00286999 | frameshift-variant | PSEN1 | GRCh38.p7 | 14:73211864 | GTCATCTAGGGCCTC[-/A]ATCGCTCTACACCTG | 5663 |
rs768879192 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73180515 | CTGAGGATTTTTCAT[A/G]TCAGTGGTTGGTTAT | 5663 |
rs768887785 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73148486 | AATATTCATTATGAT[C/T]GTACAATGCAAGGAT | 5663 |
rs768890711 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209885 | GTATTTTGGGGGGCA[C/T]AGTTCTTTGTGGGAC | 5663 |
rs768923334 | snp | A/T | 1.64727e-05 | 0.00286986 | missense | PSEN1 | GRCh38.p7 | 14:73192688 | TGGACTACATTACTG[A/T]TGCACTCCTGATCTG | 5663 |
rs768963474 | in-del | -/TA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73151879 | CAACCTAAAATATTT[-/TA]TATATATATATATAT | 5663 |
rs769003980 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73181529 | CTTGGGACCCTGAGA[C/T]GAGATGATTGCTTGA | 5663 |
rs769014163 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73144532 | TGCTGTAAACTCCTA[C/T]GGGGCAGGTTTGGAG | 5663 |
rs769045370 | snp | C/T | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135252 | TTTTGTTCTTAAATA[C/T]GAAGCTTTTGTGTGT | 5663 |
rs769059465 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73168466 | CAAGCAGCTGATTGT[C/T]GGAAATACAAGCCAC | 5663 |
rs769110935 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73176756 | TAACCCCTACTATTA[-/T]TCCCAGTTTTATGGA | 5663 |
rs769125155 | in-del | -/GCC | 4.95544e-05 | 0.00497742 | cds-indel | PSEN1 | GRCh38.p7 | 14:73170831 | GGAGCACAACGACAG[-/GCC]ACGGAGCCTTGGCCA | 5663 |
rs769248198 | in-del | -/AAT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73207150 | ATACCTTACCTCAAA[-/AAT]AATAATAATAATGAA | 5663 |
rs769265539 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | PSEN1 | GRCh38.p7 | 14:73192725 | TGGTGTGGTGGGAAT[A/G]ATTTCCATTCACTGG | 5663 |
rs769268606 | snp | A/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221706 | AGCCCATCTTATTTC[A/T]TTAAATCATTCATCT | 5663 |
rs769287839 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73212423 | CTCCCTTCAGACTTT[C/T]TAAGTTGGCATTTTA | 5663 |
rs769318960 | snp | A/C | 8.26043e-05 | 0.00642615 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192913 | GGAATGCCCCACTGG[A/C]GTGTTTTCTTTCCTC | 5663 |
rs769326615 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73186551 | GGAGTCTGAGGCGGG[C/T]GGATCACTTGAGGTC | 5663 |
rs769331360 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73191124 | GCATTTTCTTCATTA[C/T]AAAAATACTTAACAT | 5663 |
rs769384496 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73175536 | TGTTTCCTTCTAGTA[A/T]TTATTTCTGTATACT | 5663 |
rs769400575 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73192164 | ATTAATTGGCCAGGC[A/C]CCGTGGCTCATGCTT | 5663 |
rs769403471 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209341 | GCCATCAAGACCACT[A/T]GTAAACCTGATAGAA | 5663 |
rs769421795 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73205478 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 5663 |
rs769436966 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73144785 | TTTAATAGTATCTCT[A/G]CTAAATTTATTGTGT | 5663 |
rs769511346 | in-del | -/TAATC | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73141266 | ATATTGGCTGAATAA[-/TAATC]TAATCTACCACAGAT | 5663 |
rs769591585 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73151258 | TAATTCTGTTTACAA[A/G]CATTTGGTAGGTTCC | 5663 |
rs769615276 | in-del | -/TTAT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73138196 | TAAACATACTATTAT[-/TTAT]TTATTTATTTATTTA | 5663 |
rs769650189 | snp | A/G | 1.64825e-05 | 0.00287071 | missense | PSEN1 | GRCh38.p7 | 14:73170944 | ACATTGAAATATGGC[A/G]CCAAGCATGTGATCA | 5663 |
rs769743835 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73139889 | ATTGGCTTTTCACAA[A/C]GCCTTGTACGGTTTC | 5663 |
rs769758013 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73171866 | AACATTGGCTTAAAT[A/G]TTAAATCCTCAAAGA | 5663 |
rs769779308 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73215976 | AAATGAAAACAGTCC[A/G]TCCCCACAGAGACAT | 5663 |
rs769816332 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73186142 | CCTAGCACTTTGGGA[A/G]GCCAAGGCAGGTGGA | 5663 |
rs769864994 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73187042 | ATTGTTTCCACATAT[A/G]GGTCATACTTGGTAT | 5663 |
rs769889869 | in-del | -/A | | | frameshift-variant | PSEN1 | GRCh38.p7 | 14:73171018 | ACCATTAAGTCAGTC[-/A]AGCTTTTATACCCGG | 5663 |
rs769933787 | in-del | -/T | 1.64765e-05 | 0.00287019 | frameshift-variant | PSEN1 | GRCh38.p7 | 14:73217225 | CACAACCATAGCCTG[-/T]TTTCGTAGCCATATT | 5663 |
rs770011616 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73207080 | AGTCCCAGCTACATG[A/G]CCAAGGCAAGAGGAT | 5663 |
rs770033578 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73158143 | TTGGATTTTCAGTTC[G/T]GAAGCATTACAGATA | 5663 |
rs770044488 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73146049 | GAGTTAGAGGTTCCA[A/G]TGAGCGAGATCGTGC | 5663 |
rs770044935 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194661 | GCAAGCTTCGCCTCC[C/T]AGGTTCATGCCGTTC | 5663 |
rs770064198 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73193712 | CCCAGGCTGGGGTGC[A/G]GTGGCACAGTCATAG | 5663 |
rs770073474 | in-del | -/CTA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73168189 | GGCAAAACCGTATCT[-/CTA]CTAAAAATACAAAAA | 5663 |
rs770079295 | snp | A/C | 1.64827e-05 | 0.00287073 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186931 | TTGGGGTAAGTTGTG[A/C]AATTTTTGGTCTGTC | 5663 |
rs770084762 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73159896 | GGCATGATCTTGGCT[C/T]ATGGCAGCCTTCACC | 5663 |
rs770098364 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73180418 | ATAGAAACAAGTTGT[A/T]TACTTTGACACCCAG | 5663 |
rs770183013 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73146994 | CTGTAAATAAGGCTG[C/T]GCCAAGATCAAAGGA | 5663 |
rs770291603 | snp | A/G | 1.64803e-05 | 0.00287052 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217288 | GAGCTCTTAATGTCA[A/G]AACTTTGATTACACA | 5663 |
rs770310070 | snp | G/T | 3.31609e-05 | 0.00407177 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173760 | TCTTCTTATGGTTGG[G/T]TATTCTTGTCACAGT | 5663 |
rs770380350 | snp | C/G | 1.67517e-05 | 0.00289406 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192596 | TCTAAATAATGTTTT[C/G]GTGAAAATTATTGTA | 5663 |
rs770414902 | snp | C/G | 6.58957e-05 | 0.00573964 | intron-variant | PSEN1 | GRCh38.p7 | 14:73219126 | TGTCTTTCCCATCTT[C/G]TCCACAGGGTTTGTG | 5663 |
rs770447155 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73168290 | AACCTGGGCGGCGGA[C/G]GTTACAGTGAGCCCA | 5663 |
rs770452158 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73143036 | TGTTTTTGTTGTTCA[C/G]AGGGCTAAGAATGTT | 5663 |
rs770454911 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73201137 | TGTGTCGCCCAGGCT[A/G]GAGTTCAGTGGGGCG | 5663 |
rs770477463 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73207105 | GAGGATCACTTGAGC[G/T]AAGGAGTTCCGGATT | 5663 |
rs770502950 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73212255 | AGCTGGGACTACAGG[C/T]GTGCGCCACCACGCC | 5663 |
rs770547949 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73220643 | CAGTGAGCTAATGAT[A/G]TCAAGGAGGAGTTTC | 5663 |
rs770567204 | in-del | -/AAT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73207152 | CCTTACCTCAAAAAT[-/AAT]AATAATAATAATGAA | 5663 |
rs770579760 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73154986 | CTTAATTGAATCTAC[A/G]GATACACATGCCTTT | 5663 |
rs770584574 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73174208 | ATTTCCATATAATAG[C/T]ACAATCTAAGTGGGT | 5663 |
rs770586574 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73190953 | CTATTTTGGAATTTC[A/G]AAGTGGGAGAGGAAT | 5663 |
rs770625924 | snp | A/G | 1.66765e-05 | 0.00288756 | missense | PSEN1 | GRCh38.p7 | 14:73206437 | ACCCGGAAGCTCAAA[A/G]GAGAGTATCCAAAAA | 5663 |
rs770629885 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73161721 | CTGAGCCTTGGTGTC[C/T]GGGTCACACATGGCT | 5663 |
rs770710955 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73175165 | AAGTCTCGCTCTTGT[C/T]CCGCAGGCTGGAGTG | 5663 |
rs770751157 | in-del | -/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222080 | TGGAAGATTTGCAGA[-/T]TTTTTTTTCAGAGAG | 5663 |
rs770764192 | in-del | -/CTAA | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134688 | CGCCACCACGCCTGG[-/CTAA]CTTTTTTTGTATTTT | 5663 |
rs770771372 | snp | C/G | 0.000175824 | 0.0093745 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208834 | CCTAGGAGCCTGTCT[C/G]CCTCCTGCTGCCATC | 5663 |
rs770805752 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73164494 | TATGTGCCAGACACC[A/G]TGAGATACGTCTTTG | 5663 |
rs770874103 | snp | C/T | 2.28094e-05 | 0.00337701 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148156 | ACTGGATTCACTTAT[C/T]ATCTCCCCTCACCTC | 5663 |
rs770899694 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73206662 | AAAACCCAACAATAC[A/G]GTCAAAGCATCCTAG | 5663 |
rs770906089 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73185931 | TATAAACCAAGTACT[A/G]CAAAATATGAATGGT | 5663 |
rs770941176 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73149821 | TACTATTACAGTTCT[A/G]TATTGTTATAGTTCA | 5663 |
rs770945562 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209306 | ATCTTTGCAGCAGCC[A/G]CTCCAGATGGGCCGC | 5663 |
rs770945609 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73196031 | ATACAAATGAGTATC[C/T]CTACAGAGCTTTGAG | 5663 |
rs770959119 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73170644 | TGATAGATAATCTAG[A/T]CTTTTAAACTGCATA | 5663 |
rs770968582 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73214270 | GCAGTGGCTCAAGCA[C/T]CTGTAATCCCAGCAC | 5663 |
rs771002035 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | PSEN1 | GRCh38.p7 | 14:73173597 | ACAGAAGATACCGAG[A/G]CTGTGGGCCAGAGAG | 5663 |
rs771041272 | snp | C/T | 1.65184e-05 | 0.00287384 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173740 | ATCTTTGCTTTCCAC[C/T]CTGTTCTTCTTATGG | 5663 |
rs771083153 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73215873 | ACTGGTACAGCCAGT[A/G]TGGAATGTGATTTGG | 5663 |
rs771086445 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73186669 | GTGGTTCCACCTACT[C/G]AGGAGGCTTAAGCAC | 5663 |
rs771106628 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73184889 | TCCTCACTTCTCAGA[C/T]GGGGCGGCCGGGCAG | 5663 |
rs771139491 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73186215 | AGAAACTGTGTCTCT[A/G]CTAAAAATACAGAAT | 5663 |
rs771207081 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73171808 | AAGGCAAAGAATTGA[A/G]CATACTGGCGTATTA | 5663 |
rs771225789 | snp | A/T | 1.64974e-05 | 0.00287201 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217093 | TAGCAAAGAGTGACC[A/T]ACTTTTTAATATTTG | 5663 |
rs771260260 | in-del | -/AT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73164864 | GCTTCTTTTATTTTC[-/AT]ATATATATATGTTCA | 5663 |
rs771305231 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73192440 | AATGAGACCCTGGCT[C/G]AAAAACAAAAACAAA | 5663 |
rs771387543 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73146833 | GTTAGGTATGTACAC[A/G]GATTTTTGCCTTCTA | 5663 |
rs771477972 | snp | A/G | 7.39878e-05 | 0.00608181 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148111 | TACGTAGCCAGGTAC[A/G]GTGTCAGTCTCTGAA | 5663 |
rs771496092 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73210601 | AGGAGGGAGGGGGTA[G/T]AAAAGGGACTGCTGT | 5663 |
rs771515240 | snp | A/C | 0.000183158 | 0.00956793 | missense | PSEN1 | GRCh38.p7 | 14:73217191 | GGTAAAGCCTCAGCA[A/C]CAGCCAGTGGAGACT | 5663 |
rs771578178 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73170051 | ATACAAGGTAACTTC[C/T]GGACGTTGCCATGGC | 5663 |
rs771581579 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73179110 | TCCCTTTTCCATTCC[A/T]GCAGCCAAAAGTGGA | 5663 |
rs771589097 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73212189 | GATCTTGGCTCACTG[A/C]AAGCTCCACCTCCCG | 5663 |
rs771631822 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73153072 | TACATAGACAAAAAG[C/T]AAACCTATGAGCTAT | 5663 |
rs771665727 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73142424 | ACAAGCCACAAGCCC[-/T]TTGTGCTAGAGATCA | 5663 |
rs771671834 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73200331 | CTGGAGTACAGTGGC[A/G]CAATCTCAACTCACT | 5663 |
rs771695417 | snp | A/G | 8.42666e-05 | 0.00649047 | utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73147998 | GTTTTCTGTGAAACA[A/G]TATTTCTATACAGTT | 5663 |
rs771706232 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73166555 | TTAATCAGCCAATCA[A/G]GTTGTTCAGACTTGT | 5663 |
rs771754083 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73172854 | CTAGCTTACTTCAGG[A/G]TCCAGGCTGGAGCCC | 5663 |
rs771759149 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73168150 | CACCTGGGGTCAGGA[A/G]TTCAAGACCAGCCTG | 5663 |
rs771788247 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73203737 | TCTTACCTAGTGGTC[-/A]TTAGTAGAAGTGGTT | 5663 |
rs771797588 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167608 | GGGATCATTCAAACT[A/G]TAGCACCCTCCTTTA | 5663 |
rs771903795 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73142937 | GACCAGAGAGCAAAA[A/G]CACCAGAGTAGATTC | 5663 |
rs771910895 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73198520 | AGAGCCGTGCCTTTG[-/A]TAAGCTGGCAGCACT | 5663 |
rs771944685 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73173932 | AGGCAGGAGGATCAC[G/T]TGGGCCCAGGAGTTC | 5663 |
rs771981071 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73163060 | CGATTATCATCTGTA[A/G]ATTCTTATGTCACAT | 5663 |
rs772022929 | snp | C/T | 1.81155e-05 | 0.00300955 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73198125 | TCCAGCTCTCATTTA[C/T]TCCTGTAAGTATTTG | 5663 |
rs772073286 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73161126 | ACTATAGGCACTCGC[C/G]ACCATACCCACCTAA | 5663 |
rs772162506 | snp | C/G | 1.75449e-05 | 0.00296178 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171095 | GCCAGTGTGGCTTTT[C/G]TTTACAGCATGTCAT | 5663 |
rs772244037 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73177279 | TGGTTTGTTTTCTCC[-/T]TTGCATATCTCTTCT | 5663 |
rs772270177 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73148551 | TCAGGAAAAGAACGT[A/T]ATCTGTGCTGTCGGA | 5663 |
rs772286610 | snp | C/T | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136341 | GGAGCTCTGGGTTCT[C/T]CCCGCAATCGTTTCT | 5663 |
rs772288566 | snp | C/G | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135587 | GTTGGTTAGGCTGGT[C/G]TAGAACTCCCAACCT | 5663 |
rs772299592 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73169267 | CTATTCTCTTAATCT[C/T]GTTTTCTGGTTTTCT | 5663 |
rs772342582 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73156845 | TTTTTTGTAATTTTA[A/G]TAGAGATGGGGTTTC | 5663 |
rs772355448 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73182928 | GTGAAAAGCATCTCT[A/C]AAGAATGATGAGAAT | 5663 |
rs772408538 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73214254 | CCAACTATTGCTGGG[C/T]GCAGTGGCTCAAGCA | 5663 |
rs772554429 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73153098 | GCTATTTAAAGGACC[C/T]TGAGGAGAAAAAAAA | 5663 |
rs772556547 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73212203 | GCAAGCTCCACCTCC[C/T]GGGTTCAAGTGATTC | 5663 |
rs772573771 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | PSEN1 | GRCh38.p7 | 14:73192709 | TCCTGATCTGGAATT[C/T]TGGTGTGGTGGGAAT | 5663 |
rs772584138 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73160912 | TGCCGGGTTCATGCT[A/G]TTGTAGGACTTTTTA | 5663 |
rs772604841 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73157780 | GAGGTCGAGGTGGGC[A/G]ATGACTTGAGGCCAC | 5663 |
rs772667148 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73191255 | AATATATCAATTTCT[C/T]ATCTACTCTTCTCTC | 5663 |
rs772667522 | in-del | -/A | 1.6531e-05 | 0.00287493 | frameshift-variant | PSEN1 | GRCh38.p7 | 14:73170819 | ATAGAGAACGGCAGG[-/A]GCACAACGACAGACG | 5663 |
rs772717651 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73140735 | CATTTAGTCCTAAAA[C/G]TTACAGATAAGGGAT | 5663 |
rs772723346 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73200340 | AGTGGCGCAATCTCA[A/G]CTCACTGCAACCTCC | 5663 |
rs772731175 | snp | G/T | 1.64741e-05 | 0.00286998 | missense | PSEN1 | GRCh38.p7 | 14:73217194 | AAAGCCTCAGCAACA[G/T]CCAGTGGAGACTGGA | 5663 |
rs772866279 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73144683 | ATATCATAAATTAGT[A/T]TGTTAAGCCTTAGTT | 5663 |
rs772896889 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73153990 | AAGTGTTGGGATTAC[A/C]GGCATGAACCACCGT | 5663 |
rs772968643 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73161219 | GGCTCAAGCAATCCA[C/T]CTGCCTTAGCCTCCC | 5663 |
rs772978584 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73217532 | TTTCTGTTTAGGAAC[C/T]GCTGCCTCAAGCCTA | 5663 |
rs772982631 | in-del | -/AA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73150766 | TAAGACTCTGTCTCA[-/AA]AAAAAAAAAAAAAAA | 5663 |
rs772984560 | snp | C/T | 1.67874e-05 | 0.00289714 | utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73148003 | CTGTGAAACAGTATT[C/T]CTATACAGTTGCTCC | 5663 |
rs773049659 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73151543 | AAATGTTCTATAATA[A/C]AGTTATTTAATAATT | 5663 |
rs773069081 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73181036 | GATGTTCATTTTAAT[A/G]TAAATTAAAATTGGG | 5663 |
rs773074564 | snp | C/G | 1.83326e-05 | 0.00302754 | splice-donor-variant | PSEN1 | GRCh38.p7 | 14:73198130 | CTCTCATTTACTCCT[C/G]TAAGTATTTGAGAAG | 5663 |
rs773094162 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73160171 | TTATTTCTCTTTTAG[C/T]GACTTGCTTATTTTG | 5663 |
rs773099222 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219669 | TACCAAGAGGTTAGG[C/T]GAAGTGGTTTAAACC | 5663 |
rs773103376 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219528 | TCCCTCGGTGCAGAA[A/G]CTACCAGATTTGAGG | 5663 |
rs773126194 | snp | A/T | 1.64738e-05 | 0.00286995 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173559 | TTTTGTGTTTGTTTT[A/T]TTGTAGAATCTATAC | 5663 |
rs773154039 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73207435 | TAAATATTGGTGAGG[A/G]AAAAAAGGCCTTAAT | 5663 |
rs773231702 | in-del | -/ATT | 1.64727e-05 | 0.00286986 | cds-indel | PSEN1 | GRCh38.p7 | 14:73173654 | ATCATGATCAGTGTC[-/ATT]GTTGTCATGACTATC | 5663 |
rs773249325 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73195765 | GACCTCCTAGCTTCA[A/G]GCAGCCTCCCAAAGT | 5663 |
rs773277617 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73208420 | TCTCTGCAGCTCTCA[A/G]TGGAGAGGAGACCTG | 5663 |
rs773293119 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73204569 | GAATATGTGACACAC[A/G]AAACCTGAAATGTTT | 5663 |
rs773295728 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221893 | CGGTGGTTATAGAGT[C/T]GGGCAAAACCAGCAG | 5663 |
rs773295865 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73196032 | TACAAATGAGTATCT[C/G]TACAGAGCTTTGAGT | 5663 |
rs773348117 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73213462 | TGCTAACTTCAGATC[A/G]GTATTTTCTTTCTCT | 5663 |
rs773370438 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73181843 | TAGTGGCACTGTCTC[A/G]GCTCACTGCACCCTA | 5663 |
rs773375606 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73149730 | TTGTCTACCAGAGTA[G/T]AATCAAATTGAAATA | 5663 |
rs773415447 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73217696 | GCAGTGTTACTTAAG[-/A]CAGCAAGCATCTAGT | 5663 |
rs773432199 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73155669 | CCACCATGCCTGGCT[A/G]ATTTTTTTTGCTGTT | 5663 |
rs773436137 | in-del | -/A | 6.59141e-05 | 0.00574045 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217287 | AGAGCTCTTAATGTC[-/A]AAACTTTGATTACAC | 5663 |
rs773522234 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73156883 | TAGCCAGGATGATCT[C/T]GATCTCCTGACCTTG | 5663 |
rs773607443 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73159319 | TCCAAACAGCTAGGA[A/C]TACAGATGTGTGCCA | 5663 |
rs773609090 | in-del | -/TTTTTTTTTTTTTTT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73140203 | CTTTTTTTGCTATTC[-/TTTTTTTTTTTTTTT]TTTTTTTTTTTGAGA | 5663 |
rs773627483 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73161060 | GCTCACTGCAACTTC[C/T]GCCTCCCAGGCTCAA | 5663 |
rs773691733 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221894 | GGTGGTTATAGAGTC[A/G]GGCAAAACCAGCAGT | 5663 |
rs773742540 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73144919 | ATTTTTTGAGATGCA[A/G]TCTTGCTCTGTCACC | 5663 |
rs773743795 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73197768 | CCTATACCCCAGTAA[C/T]GATACACTGTACACT | 5663 |
rs773786642 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73192388 | AAAGACTGCAGTGAG[A/C]CGTGATTGCACCACT | 5663 |
rs773808222 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209602 | TAGTCTATTTGGAGA[A/G]ATAGATGGTCAACAA | 5663 |
rs773862128 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73153714 | ATACATTTTCTTTCC[-/T]TTTTTTTTTTTTTTT | 5663 |
rs773871073 | snp | A/G | 1.70133e-05 | 0.00291657 | utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73147990 | GAGGCTTTGTTTTCT[A/G]TGAAACAGTATTTCT | 5663 |
rs773894710 | in-del | -/ACC | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73157547 | ATGTATACTCTTGAA[-/ACC]ACCACCACAGTTAAA | 5663 |
rs773933271 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73139244 | GCCGAGATCGCGCCA[C/T]TGCACTCCAGCCTGG | 5663 |
rs774025917 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73217323 | CTTTAAGGCAGTTCT[A/G]TTTTAACCCCAGGTG | 5663 |
rs774033846 | snp | A/C/T | 0.000230599 | 0.0107357 | missense | PSEN1 | GRCh38.p7 | 14:73211793 | GGGAGTCACAAGACA[A/C/T]TGTTGCAGAGAATGA | 5663 |
rs774052358 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73152894 | TTAAAAATACAAAAA[G/T]TAGCCAGGTGTGGTG | 5663 |
rs774071224 | in-del | -/TA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73174093 | TTAGTTATCAAGATT[-/TA]GTGATAATTTATGTT | 5663 |
rs774081621 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73140292 | CTCAGCTCACTGCAA[C/T]GTCCGCCTCCCAGGT | 5663 |
rs774257366 | snp | C/T | 1.64808e-05 | 0.00287057 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73170970 | GATCATGCTCTTTGT[C/T]CCTGTGACTCTCTGC | 5663 |
rs774315727 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73171944 | TTCTCATAGCAACTT[G/T]TCCTTTCTCACTTGT | 5663 |
rs774380907 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73171428 | GTGTTATATATAAAG[-/T]TTTGGTGCCGCAAAA | 5663 |
rs774382919 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73207218 | CCTCTAAGGATACTA[C/T]AGAACATATTAAGGA | 5663 |
rs774433313 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194740 | CGCCCGGCTATTTTT[C/T]TGTATTTGTAGTAGA | 5663 |
rs774501327 | snp | A/G | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135493 | CTGCTGCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 5663 |
rs774610514 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73181585 | GAAACATAGTGAGAC[C/G]CCAGTCTCTTAAAAA | 5663 |
rs774672464 | in-del | -/TAGCAACTTGTCCTTTCTC | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73171935 | TGGTATCTTTTCTCA[-/TAGCAACTTGTCCTTTCTC]ACTTGTCACAATTTG | 5663 |
rs774687713 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73148537 | TTCAAAGGAGGGATT[C/G]AGGAAAAGAACGTAA | 5663 |
rs774691383 | snp | A/G | 1.64754e-05 | 0.00287009 | intron-variant | PSEN1 | GRCh38.p7 | 14:73219110 | ATTATGTGTGAATGT[A/G]TGTCTTTCCCATCTT | 5663 |
rs774724179 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73189043 | TGATCCACCTGCCTC[C/T]GCCTCCCAAAATGCT | 5663 |
rs774744015 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73169125 | TGTAAAACCCTTGAT[C/G]AACTTCCCATTGTCA | 5663 |
rs774769033 | snp | C/T | 1.65034e-05 | 0.00287253 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186966 | AGAATTAACTACCTT[C/T]GTGCTGTGTAGCTAT | 5663 |
rs774839177 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73163930 | GATCTCATTTTGTTT[-/A]AAAAAAAAAAAATCA | 5663 |
rs774873715 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73214117 | GATAATAAATGTGGT[A/G]TATTCATACAATGGA | 5663 |
rs774881214 | in-del | -/AA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73214531 | GCGAAACTCCATCTC[-/AA]AAAAAAAAAAAAAAA | 5663 |
rs774903216 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73155389 | GATAAACTGAATGAT[A/T]AGTACACTACCTAGC | 5663 |
rs774915811 | snp | C/G | 1.64874e-05 | 0.00287113 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186809 | TCTGTACTTTTTAAG[C/G]GTTGTGGGACCTGTT | 5663 |
rs774927657 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73189771 | CACTGGTGAAGCAGA[C/G]ATGCCAGCTGAGGTC | 5663 |
rs775004563 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73156607 | ATAAATTGCACATGG[A/G]CTTCATTGTACATTT | 5663 |
rs775064441 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73163568 | CTAAGAATAGTCAAG[G/T]GACAAACAGGAGCTA | 5663 |
rs775081461 | in-del | -/T | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136065 | CACCAGAAGTTTTGA[-/T]TTCATTGAGTGGTGG | 5663 |
rs775084558 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73144846 | TAATCACTTCTGCTC[A/G]TATTTAACCTATAAG | 5663 |
rs775130003 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73150044 | GCTGAAGTTGTGTTT[C/G]TTTTTTTAGCCCAAA | 5663 |
rs775131890 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73192167 | AATTGGCCAGGCACC[A/G]TGGCTCATGCTTGTA | 5663 |
rs775150562 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73177012 | CCTTTTTGAACCTAA[A/T]TTTTTCTGGACCTTA | 5663 |
rs775165798 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73198714 | ATCAATAGTTCTAGC[A/G]ACTGAGGAGAGAAGT | 5663 |
rs775187206 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73164875 | TTTCATATATATATA[C/T]GTTCATTCATAAATT | 5663 |
rs775199656 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209435 | TAAAGAAAATCAAAT[A/G]ATTGTCTGTGAGCAT | 5663 |
rs775219738 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73151284 | GTTCCAGTTTTTCAC[A/G]ATAACTGACAGTGCT | 5663 |
rs775379696 | snp | A/G | 0.000349528 | 0.0132152 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208862 | ATCAACCTGCTGTCT[A/G]TAGCTCCCATGGCAC | 5663 |
rs775450575 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73186187 | GAGTTCGAGACCAGC[A/C]TGACCAACATGGAGA | 5663 |
rs775509900 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73148789 | AATACAAAAATTAGC[C/T]GGGCTTGGTGGCAGG | 5663 |
rs775543665 | snp | A/G | 1.65277e-05 | 0.00287464 | missense | PSEN1 | GRCh38.p7 | 14:73170827 | CGGCAGGAGCACAAC[A/G]ACAGACGGAGCCTTG | 5663 |
rs775595014 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73216968 | CCTATTGTAGAAAAC[A/C]AAAAAAGAAAGAAAA | 5663 |
rs775607010 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73156349 | CAACACAGCCAGACT[C/T]GGTCTCAAAAAATAA | 5663 |
rs775607266 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73158470 | AGCTGGGATTACAGG[C/T]GCCTGCCACCACACC | 5663 |
rs775624520 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73171885 | AATCCTCAAAGATAA[C/T]ATTCCTGTTTCTCCT | 5663 |
rs775688144 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73193768 | CTCATGCGATCCTCC[C/T]ACTTCAGCCTCTCAA | 5663 |
rs775735358 | snp | A/C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194672 | CTCCCAGGTTCATGC[A/C/T]GTTCTCCTGCCTCAG | 5663 |
rs775771736 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73186344 | AGATTGCGCCATTGC[A/G]CTCCATTCTGGGCAA | 5663 |
rs775818382 | in-del | -/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73140335 | TCTGCCTCAGCCTCC[-/C]GAGTAGCTGGGACTA | 5663 |
rs775822513 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223321 | CCTGAGCCCTGACAT[A/G]TGGTGGCAGCATTGC | 5663 |
rs775877656 | snp | A/G | 0.000115328 | 0.0075928 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73217136 | TTTAGGGGGAGTAAA[A/G]CTTGGATTGGGAGAT | 5663 |
rs775926772 | snp | C/T | 1.66377e-05 | 0.00288419 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173772 | TGGGTATTCTTGTCA[C/T]AGTAACTTAACTGAT | 5663 |
rs775952558 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73180446 | CAGTATAACTAAAAG[G/T]ATCTTTTGAGTCAGA | 5663 |
rs776021459 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73188658 | TAAATAAATAACTAA[A/G]TCTCTAACATTATAA | 5663 |
rs776030866 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73189927 | GTAGCAGGTGTAGAC[G/T]GAGCTGGCCTCTAAC | 5663 |
rs776052794 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73200426 | AGGCGCATGCCACCA[A/C]GCCTGGCTGATTTTT | 5663 |
rs776054093 | snp | A/G | 1.67298e-05 | 0.00289217 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192599 | AAATAATGTTTTGGT[A/G]AAAATTATTGTACAT | 5663 |
rs776071448 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219579 | ATAGGCCCGGAAGTT[A/G]CTGTGCCCCATCAGC | 5663 |
rs776076782 | snp | A/C/G | 8.2549e-05 | 0.00642406 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219332 | GTTTCTTCTTTGACT[A/C/G]TAACAAAATCTGGGG | 5663 |
rs776078701 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73210202 | TCAGGATAAATTAGT[C/T]ATAGATAATAATATA | 5663 |
rs776123451 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73213159 | TCCTGGAAAAGTAGA[C/T]GTATCTGCCTGCTCT | 5663 |
rs776145632 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73154190 | TTGTAAACACAACTA[C/T]GTATACCTGTGTGTA | 5663 |
rs776191347 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73173668 | CATTGTTGTCATGAC[C/T]ATCCTCCTGGTGGTT | 5663 |
rs776233959 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73155083 | TATCCTATAAAAATA[C/T]TACCATAGAAGTGCC | 5663 |
rs776233980 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73142125 | TAATTTCAATTATAG[G/T]TTGGAATTTAGAGTT | 5663 |
rs776265311 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73142601 | GAAGAAAACGTATTA[A/G]TTCTTTTCTGTTGGT | 5663 |
rs776278107 | snp | C/T | 1.64746e-05 | 0.00287002 | missense | PSEN1 | GRCh38.p7 | 14:73219143 | CCACAGGGTTTGTGC[C/T]TTACATTATTACTCC | 5663 |
rs776305367 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209319 | CCACTCCAGATGGGC[C/T]GCTGCTGCCATCAAG | 5663 |
rs776307607 | in-del | -/AT | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134524 | TTTATTTATTTATTT[-/AT]TTATTTATTTTTATT | 5663 |
rs776322523 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73220657 | TGTCAAGGAGGAGTT[A/T]CAGGTTATTCTCGTC | 5663 |
rs776343736 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73170762 | GATTCTGCTGAGAAT[C/T]TGATTTACTGAAAAT | 5663 |
rs776378886 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73163482 | ACTCAACAAATATTT[A/G]TAGAGTACAGGAGAC | 5663 |
rs776392455 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73143080 | GTTAAAAAGTCTCCT[A/G]GTGTCTTTTGCCACG | 5663 |
rs776410239 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73149908 | CTTCATTTCTTCAAC[C/T]CTAAGCAAATACTGT | 5663 |
rs776429004 | snp | A/T | 4.72367e-05 | 0.00485964 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198154 | TGAGAAGGATATTGA[A/T]TTAGTAATCAGTGTA | 5663 |
rs776454017 | in-del | -/TG | | | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73223735 | ATCATAATGTATAAC[-/TG]TAACTCACAGAACTG | 5663 |
rs776497303 | snp | G/T | | | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137514 | TCAATTCCATAGATT[G/T]CCAGTTGATGTTGGA | 5663 |
rs776529193 | snp | A/T | 0.000302297 | 0.0122905 | intron-variant | PSEN1 | GRCh38.p7 | 14:73159995 | GCCTCGCTAATTTTT[A/T]AATTTTTTTGTAGAG | 5663 |
rs776529290 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73208587 | CGGAGTGGGTAGCTT[C/T]TTTCTGCAGGCAGGT | 5663 |
rs776584385 | snp | C/G | 1.65414e-05 | 0.00287583 | missense | PSEN1 | GRCh38.p7 | 14:73170815 | GACAATAGAGAACGG[C/G]AGGAGCACAACGACA | 5663 |
rs776645110 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73178216 | GAGCCACCACACCCG[A/G]CCCTTTTTTTTTTTT | 5663 |
rs776652612 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73214306 | AAGGCCAAGGCAGGC[A/G]GACCACCTGAGATCA | 5663 |
rs776680562 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73186024 | CATTTTTGTAACAAA[A/G]TGTTGGAAAATTTTT | 5663 |
rs776683638 | in-del | -/CC | 4.95487e-05 | 0.00497714 | frameshift-variant | PSEN1 | GRCh38.p7 | 14:73170832 | GAGCACAACGACAGA[-/CC]CGGAGCCTTGGCCAC | 5663 |
rs776759540 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73192568 | ATCTAATGTTTGGGA[G/T]CCATCACATTATTCT | 5663 |
rs776855719 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73185786 | GAACTCCTGGCCTCA[C/T]GATCCGCCTGCCGTG | 5663 |
rs776865810 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73153809 | CCTCTGCCTCCCAGG[C/T]TCAAGCGATTCTCCT | 5663 |
rs776902006 | snp | A/C | 1.64727e-05 | 0.00286986 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73173605 | TACCGAGACTGTGGG[A/C]CAGAGAGCCCTGCAC | 5663 |
rs777002360 | in-del | -/TCG | 3.29487e-05 | 0.00405872 | cds-indel | PSEN1 | GRCh38.p7 | 14:73211865 | TCATCTAGGGCCTCA[-/TCG]TCGCTCTACACCTGA | 5663 |
rs777033516 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73161436 | ATTGTACAGGATATT[A/T]GGGGATCTGTAAGAC | 5663 |
rs777059591 | snp | G/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223150 | GAGACATCTGCATGT[G/T]ATCATCTGCATAGTC | 5663 |
rs777093611 | snp | A/T | 1.64836e-05 | 0.0028708 | missense | PSEN1 | GRCh38.p7 | 14:73211914 | GGAACTTTCCAGCAG[A/T]ATCCTCGCTGGTGAA | 5663 |
rs777162837 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73177330 | ATAAATCAAATGAAT[C/T]ATCCTTCATACCATT | 5663 |
rs777182161 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73210628 | CTGTTTTCATTTATA[A/C]ATCTTATTCTTATAT | 5663 |
rs777198993 | snp | C/T | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134716 | TATTTTTAGTAGAGA[C/T]GGGGTTTCTCCATGT | 5663 |
rs777214326 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73165252 | TGAGCCACCACGCCC[A/G]GCCCAAACTGTGCTT | 5663 |
rs777308508 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73181429 | GCAACAAGAGCAAAA[C/T]TCCATCTCAAAATCA | 5663 |
rs777338735 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73166573 | TGTTCAGACTTGTAC[C/T]GCTGAACATCAATTG | 5663 |
rs777354891 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73154911 | GAGGTTGTAGGGAAA[C/T]AGGCTTTCTTGTATG | 5663 |
rs777371921 | snp | C/G | 1.65754e-05 | 0.00287879 | missense | PSEN1 | GRCh38.p7 | 14:73170807 | TATAGAATGACAATA[C/G]AGAACGGCAGGAGCA | 5663 |
rs777388604 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73168159 | TCAGGAGTTCAAGAC[C/T]AGCCTGGCCAACATG | 5663 |
rs777427451 | snp | C/T | 1.64914e-05 | 0.00287149 | missense | PSEN1 | GRCh38.p7 | 14:73170887 | CCCCAGGGTAACTCC[C/T]GGCAGGTGGTGGAGC | 5663 |
rs777452039 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73202040 | ACGTGAGCCACTGCA[C/T]CCGACCTGTTTTATT | 5663 |
rs777504271 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73143008 | AAGATCCTCAGATCT[A/G]GGTAACTGTTGTTGT | 5663 |
rs777545298 | snp | G/T | 1.66391e-05 | 0.00288431 | missense | PSEN1 | GRCh38.p7 | 14:73206430 | GAAGGAGACCCGGAA[G/T]CTCAAAGGAGAGTAT | 5663 |
rs777599148 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73181147 | TTTTGTCATTTAAAA[A/G]TCATAGTTTCAGCTG | 5663 |
rs777633668 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73191880 | ATGACTGCTAAATCT[C/T]ATTGTATGAAAATTT | 5663 |
rs777640525 | snp | A/G | 4.94328e-05 | 0.00497131 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73186894 | ATCTCTATTGTTGCT[A/G]TTCTTTTTTTCATTC | 5663 |
rs777657015 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73144200 | TGCACGTCACCATGC[C/T]TGGCTAATTTTTGTA | 5663 |
rs777707569 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73166143 | GTATGTTACTGTTAA[A/G]TTAAACAGTGTTCTA | 5663 |
rs777708529 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73175059 | GGCATGGTGGCTCAT[A/G]CCTGTAATCCCAGCA | 5663 |
rs777725110 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220349 | TTCCACAGCAAATGA[A/G]ATGTATGCCCAAAGA | 5663 |
rs777734426 | snp | A/T | 1.64746e-05 | 0.00287002 | missense | PSEN1 | GRCh38.p7 | 14:73217236 | GCCTGTTTCGTAGCC[A/T]TATTAATTGTAAGTA | 5663 |
rs777738696 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73197197 | CTCGGCCTCCCAAAG[C/T]GCTGGGATTGCAGGC | 5663 |
rs777835081 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73163427 | TACAAAAAATTAGCC[A/G]AGCTTCACAAACAAT | 5663 |
rs777839620 | snp | A/C | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221472 | GTGTGTATTTAAATC[A/C]ATCCTATGTATTACT | 5663 |
rs777923890 | snp | C/T | 1.65029e-05 | 0.00287248 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173727 | GCATGAGACACAGAT[C/T]TTTGCTTTCCACCCT | 5663 |
rs777972216 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73187901 | TTCAAAAGCATAACA[A/G]AATATTAAGAGAATT | 5663 |
rs777972716 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73169664 | ATTCAACCTTACCAA[-/T]TTTTTTTTTTTTTTT | 5663 |
rs778020454 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73210031 | ACTCCCCGGAAGGGA[C/G]GTGCTATCCCTAGTT | 5663 |
rs778021679 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73216575 | ACCAGCCTGACCAAC[A/G]TGGTGAAACCCTGTC | 5663 |
rs778082529 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73171737 | GGTAACTGGAATGAG[A/G]GTGGAGCAGGTAATG | 5663 |
rs778115998 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73186646 | GCCTAGCGTGGTGGC[A/G]CGCACGCGTGGTTCC | 5663 |
rs778174421 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73214319 | GCGGACCACCTGAGA[A/T]CAGGAGTTCGAGACC | 5663 |
rs778187959 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73141239 | CCTTGGCCAGGCTGG[A/G]GGAGGGAGTGAATAT | 5663 |
rs778204949 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73172363 | CTAAGACAGCAGGTG[A/G]AGGGCAGGGGTTAGA | 5663 |
rs778214742 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73139591 | TAAGAAAAAAAGAAA[A/G]AAAAGGGGGGCAAAA | 5663 |
rs778227735 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73157838 | TAAAAATGCAAAAAT[C/T]AGCCAGGGGTGGTGG | 5663 |
rs778244504 | snp | G/T | 1.66059e-05 | 0.00288144 | missense | PSEN1 | GRCh38.p7 | 14:73206412 | TGGTTGGTGAATATG[G/T]CAGAAGGAGACCCGG | 5663 |
rs778258373 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73159633 | TTGCAAAAATCAGTT[G/T]TCCATATATGTGTCA | 5663 |
rs778289613 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73163269 | CAAATCTCTGAAACC[C/G]AAAACTGCAATCTAA | 5663 |
rs778329014 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73190522 | TAAAATATGCTATCA[C/T]TTGTGTCAAGTAGAA | 5663 |
rs778426900 | snp | A/C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73146821 | GTATTAATTAGCGTT[A/C/T]GGTATGTACACGGAT | 5663 |
rs778465743 | snp | G/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221527 | AATTATTCTGTCTCT[G/T]TCTCCAAGTTTGAGC | 5663 |
rs778482194 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73155434 | TAAATATTAACATTT[C/T]TTATCAAAATTGCCA | 5663 |
rs778499746 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73168096 | TGCGGTGGCTCACTC[C/T]TATAATCCCAGCACT | 5663 |
rs778520389 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73153937 | CAGGCTGGTCTCGAA[C/G]TCCTGACCTCAAGTG | 5663 |
rs778599229 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73178960 | TAATTCGGTTGTCAG[C/G]GTCGGTGTGTACTGT | 5663 |
rs778610057 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73199319 | AGAGAAGAGGAAGAC[A/C]AGGGTCAAACTTTGT | 5663 |
rs778630379 | snp | A/G | 1.6483e-05 | 0.00287076 | missense | PSEN1 | GRCh38.p7 | 14:73173703 | ATAAATACAGGTGCT[A/G]TAAGGTGAGCATGAG | 5663 |
rs778710007 | snp | A/G | | | | | GRCh38.p7 | 14:73200983 | TTGAACCCAGGAGGC[A/G]GAGGTTACAGTGAGC | 5663 |
rs778740074 | in-del | -/CCCACTGGAGT | 1.65037e-05 | 0.00287256 | | | GRCh38.p7 | 14:73192905 | TTGTCACAGGAATGC[-/CCCACTGGAGT]GTTTTCTTTCCTCAT | 5663 |
rs778756870 | snp | C/T | | | | | GRCh38.p7 | 14:73201907 | ACCCACCACCACATC[C/T]GGCTAATGTTTGTAT | 5663 |
rs778762943 | in-del | -/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73182394 | CCTAGGTACTAGGGA[-/G]GCTGAGGTGGGAGTA | 5663 |
rs778775855 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73190756 | CTAAAGAGGGGAACC[A/G]TGGGGCACAGTGGGG | 5663 |
rs778783858 | snp | C/T | 1.7164e-05 | 0.00292945 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211987 | ATGGATTCCTTTAGG[C/T]AGCTACATTATCAAC | 5663 |
rs778787403 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73141432 | TCCTAGTCTCTTAAA[A/G]ACCAGAGGAGTCTTT | 5663 |
rs778800054 | snp | A/G | 6.58989e-05 | 0.00573978 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73211884 | CTCTACACCTGAGTC[A/G]CGAGCTGCTGTCCAG | 5663 |
rs778830763 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73174889 | CTCGCTCTTTTGCCA[A/G]AGTGACCTACTGCTG | 5663 |
rs778850133 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73189486 | GCGTGGTGGTGGGTG[C/T]CTGTAATTCCAGCTA | 5663 |
rs778861365 | snp | G/T | 1.71466e-05 | 0.00292797 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171085 | TATTCTCAAAGCCAG[G/T]GTGGCTTTTCTTTAC | 5663 |
rs778876451 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73154780 | TATTTATGGAGTAAG[A/G]AATAGAAATGGCAAT | 5663 |
rs778879417 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73142787 | TTAAAATCTCTTTGT[A/G]TATAATAGATAAATG | 5663 |
rs778894976 | in-del | -/TTTTTCTTACA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73203420 | ACAGAATGTAAGAAT[-/TTTTTCTTACA]TTTTTCTTACATTTT | 5663 |
rs778988601 | in-del | -/CA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73176844 | ATGGACATTTGAGTC[-/CA]GAGTTTGGCCTGGAT | 5663 |
rs779040789 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73195687 | GCTTCAAAAGCCTGG[A/G]CTCAAGCAGTCCTCC | 5663 |
rs779105967 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73160871 | GGAATGCAGTGGCGC[A/G]ATCTTGGCTCACTGC | 5663 |
rs779123784 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209093 | CTGAAATCGGAGCCT[A/G]CAGACGCAAGGGGCT | 5663 |
rs779144093 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73147579 | TCAGAAGTCATTAAG[C/T]ATCTTTGTGGTTGAA | 5663 |
rs779158922 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221247 | TTCCATGAAATCCCT[C/T]CTTCCAAGATTCATT | 5663 |
rs779160409 | snp | A/G | 1.64798e-05 | 0.00287047 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73192860 | GGCTGTGATTTCAGT[A/G]TATGGTAAAACCCAA | 5663 |
rs779172731 | snp | A/C/G | | | intron-variant, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73138112 | TCTTTTGGAGAAAAG[A/C/G]CATACAAATTTATTA | 5663 |
rs779215109 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73182800 | GCCAAGACCATGCTA[C/T]TGCACTCCAGCCTGG | 5663 |
rs779296437 | snp | A/T | 1.6473e-05 | 0.00286988 | missense | PSEN1 | GRCh38.p7 | 14:73192699 | ACTGTTGCACTCCTG[A/T]TCTGGAATTTTGGTG | 5663 |
rs779339899 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73170399 | AAGGATTTTAAAGTC[C/T]TATTAATTAAGGTAA | 5663 |
rs779341876 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73186474 | GTACTATTTTATAAA[G/T]TTGTTTTAAAGAGAG | 5663 |
rs779358938 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73156830 | ACCATGCCCAGCTAA[G/T]TTTTTGTAATTTTAG | 5663 |
rs779466339 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73171485 | CCTTTTAATTCTCAG[C/T]AAGGCAAGTTACTTC | 5663 |
rs779479373 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73214035 | GACACATATACAATG[A/G]TCATAGTAATATTGT | 5663 |
rs779524422 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73216493 | AGGCCATGTGTGGTG[G/T]CTCACGTCTGTAATC | 5663 |
rs779526477 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73149585 | GAAAATTCTTTCCCA[C/G]CTGGGAAGTTTTGAT | 5663 |
rs779562506 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73215394 | TTTGAGACCAGCCTG[G/T]CCAACATGGTAAAAC | 5663 |
rs779628997 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73146686 | CTTTATGCATTTTTG[A/G]TGAAAAATCATTAGA | 5663 |
rs779635524 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73178810 | GATTTTGATATTTTT[A/G]TTTTATTGGCCAATT | 5663 |
rs779723081 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73145676 | TCACTGAAAGTGAAC[G/T]TGTATGGATACTCAA | 5663 |
rs779741460 | in-del | -/AA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73151415 | TGCTAGGATTCTTCC[-/AA]AGTGTATATTGCAGG | 5663 |
rs779764234 | snp | C/T | | | stop-gained | PSEN1 | GRCh38.p7 | 14:73219275 | CAATTAGCATTCCAT[C/T]AATTTTATATCTAGC | 5663 |
rs779797170 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73176257 | GAAGCATTCACCTCC[C/T]CCACTTTAAAAATGC | 5663 |
rs779896806 | snp | G/T | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135154 | CTTGTTAAAGTGGGG[G/T]AGGTGAAGAATTTTA | 5663 |
rs779909280 | snp | C/T | 1.69565e-05 | 0.00291169 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171072 | AGTTTTGTTTTATTA[C/T]TCTCAAAGCCAGTGT | 5663 |
rs779925337 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73211438 | GCTTCACCACTCATA[A/G]GTTCATACCAAGTTA | 5663 |
rs779934292 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73141284 | TCTAATCTACCACAG[A/G]TGGTTAACAGAGGTG | 5663 |
rs779938793 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73152734 | TTCAGTTATGTTTCT[C/T]AGTCTCCATTTGAAA | 5663 |
rs779946625 | in-del | -/T | | | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137725 | AAAGGTTGGCAGGGA[-/T]TTTTGAGTGTTAGGC | 5663 |
rs779972537 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73200162 | TTTTTTATTGTTTGT[C/T]TAATGCTTTGGGTGA | 5663 |
rs779985031 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73205504 | AAAAAAAAAAAAATT[A/T]CTGTGACCAGATTGG | 5663 |
rs780007791 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73218975 | TAGGTTTTTTTCATA[A/G]CTCTTCTTCCAGATT | 5663 |
rs780028694 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73153782 | CAGTTGTGCGATCTC[A/G]GCTCACTGCAGCCTC | 5663 |
rs780119074 | snp | A/G | 1.64768e-05 | 0.00287021 | missense | PSEN1 | GRCh38.p7 | 14:73219273 | ACCAATTAGCATTCC[A/G]TCAATTTTATATCTA | 5663 |
rs780136568 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73142594 | AGTGAGAGAAGAAAA[C/T]GTATTAATTCTTTTC | 5663 |
rs780188948 | in-del | -/TCC | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73213384 | AGAGGGCTCTTTGTG[-/TCC]TCCTCCTCCTCTTCG | 5663 |
rs780194755 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73188248 | AATACATTTGACCAA[C/G]TGGAGTTTGTTTGCA | 5663 |
rs780199521 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73150765 | GTAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 5663 |
rs780232050 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73192839 | ATGGACTGCGTGGCT[C/T]ATCTTGGCTGTGATT | 5663 |
rs780250515 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73189325 | AATTAAACAAAAGTC[C/T]CCTGTCTGGGTGCCG | 5663 |
rs780265274 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73162510 | CACGCGAACAAGCGA[A/T]TGAGTGAGAGAGAGA | 5663 |
rs780318337 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73149295 | AAGAGTTTGAGTCCA[G/T]CATGGGCAACATAGA | 5663 |
rs780323099 | snp | A/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219813 | GAATGGGGAATGGAG[A/T]GGTGGGCAGGGGTTC | 5663 |
rs780340603 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73211464 | AGTTACAACCCCACA[A/G]CCTTAGAGCTTTTGT | 5663 |
rs780354109 | in-del | -/TTTA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73176400 | ACTTTTGTTCTTCTG[-/TTTA]TTTCTCAGATTTTAT | 5663 |
rs780371151 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73173716 | CTATAAGGTGAGCAT[C/G]AGACACAGATCTTTG | 5663 |
rs780407573 | in-del | -/CACT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73168962 | TTGCTCTGATTCCCA[-/CACT]CACTCACTCGCTTGC | 5663 |
rs780407685 | snp | C/G | 3.29897e-05 | 0.00406125 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186950 | TTTTGGTCTGTCTTT[C/G]AGAATTAACTACCTT | 5663 |
rs780411078 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73148402 | ACCTATCTTGCTCTT[A/T]TTCTTCTACGGCTGA | 5663 |
rs780414593 | in-del | -/C | 1.80153e-05 | 0.00300122 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206481 | GCAGAAAGTAGGTAA[-/C]TTTTATTAGATAATA | 5663 |
rs780429161 | snp | C/T | 1.64798e-05 | 0.00287047 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217291 | CTCTTAATGTCAAAA[C/T]TTTGATTACACAGTC | 5663 |
rs780461228 | snp | G/T | 1.64732e-05 | 0.0028699 | missense | PSEN1 | GRCh38.p7 | 14:73192673 | CCTATAACGTTGCTG[G/T]GGACTACATTACTGT | 5663 |
rs780461288 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73217336 | CTGTTTTAACCCCAG[G/T]TGGGTTAAATATTCC | 5663 |
rs780472853 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73147151 | CCACCACACCCGGCT[A/G]ATTTTTGTATTTTTA | 5663 |
rs780591217 | snp | A/G | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136289 | ACAACCCACGCCAGC[A/G]CTCTGGGCGGATTCC | 5663 |
rs780639187 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73149973 | TTTGTGGGCTGCTGT[A/G]CATAATCTCATTCAT | 5663 |
rs780676862 | snp | C/T | 1.66969e-05 | 0.00288932 | intron-variant | PSEN1 | GRCh38.p7 | 14:73170794 | TTTTTCTTGTGCTTA[C/T]AGAATGACAATAGAG | 5663 |
rs780676930 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73182699 | AAAAATCACCTGGGC[A/G]TTGGTGGTGGGTGCC | 5663 |
rs780723983 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73203377 | ACAGGCATGAGCCAC[C/T]GCACCTGGCCTTCGT | 5663 |
rs780729803 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73170328 | GTAGGTCTTGGCCTT[A/C]TTTTACCCAGCCCCT | 5663 |
rs780743099 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73213920 | TAGTATAGTGATTTT[C/G]GAAAACAGTTCGGTA | 5663 |
rs780763938 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73192096 | TTCCTATTAAGAAAA[A/T]GTTCAGCTTGGGAAA | 5663 |
rs780780565 | snp | C/T | 0.000175762 | 0.00937285 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208835 | CTAGGAGCCTGTCTG[C/T]CTCCTGCTGCCATCA | 5663 |
rs780796290 | snp | A/G | 1.68066e-05 | 0.00289879 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171063 | GTACGTATGAGTTTT[A/G]TTTTATTATTCTCAA | 5663 |
rs780806907 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221691 | AGTAGCTGAGACTAC[A/G]GCCCATCTTATTTCT | 5663 |
rs780832310 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73190967 | CAAAGTGGGAGAGGA[A/G]TCATCTTTTTGGATG | 5663 |
rs780856298 | in-del | -/AT | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223319 | ACCCTGAGCCCTGAC[-/AT]GTGGTGGCAGCATTG | 5663 |
rs780875908 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73214905 | AGTGTCTTTGAACGG[C/T]GAACTTAAAAAGGGT | 5663 |
rs780917786 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73148084 | CTGAGGACAACCACC[C/T]GAGCAATACTGTACG | 5663 |
rs780973605 | in-del | -/TAAT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73140615 | TTCACTATAGCTTAA[-/TAAT]TTGTTTGCTTTTCTG | 5663 |
rs781032617 | in-del | -/TTT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73158071 | ATGTTATGTGGTTCC[-/TTT]TTATTGCTGAGTTGT | 5663 |
rs781049812 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73144511 | TCAAAATACCGTAAT[A/C]CTCATTGCTGTAAAC | 5663 |
rs781067422 | snp | C/T | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134770 | TGACCTCAGATGAGC[C/T]GCCCACCTTGGCCTC | 5663 |
rs781076758 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73152266 | ATCAAGCATTCGAGG[G/T]TTTCTGTGATGACTG | 5663 |
rs781136392 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73207136 | ACCCTGGGCAACTTA[C/T]ACCTTACCTCAAAAA | 5663 |
rs781182079 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73210287 | TCAAAAAAGCAAATG[C/T]AATTATAGTATATTC | 5663 |
rs781376659 | snp | G/T | 1.64795e-05 | 0.00287045 | missense | PSEN1 | GRCh38.p7 | 14:73186919 | TCATTCATTTACTTG[G/T]GGTAAGTTGTGAAAT | 5663 |
rs781386633 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73173460 | AAAAGTGACTTATAA[G/T]ATACGAATTGAATTA | 5663 |
rs781401368 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209027 | GCTGCCCCAAGCGCC[C/T]GCACACCCGGCCAGG | 5663 |
rs781429135 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73218822 | ACAGAGGCCAACACA[G/T]CATTTAAGATAGAAA | 5663 |
rs781431904 | snp | A/G | 1.64751e-05 | 0.00287007 | missense | PSEN1 | GRCh38.p7 | 14:73192663 | GTGTTTAAAACCTAT[A/G]ACGTTGCTGTGGACT | 5663 |
rs781435448 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73206621 | CAGTAAATACACAGA[C/T]AAGTATTTAAGGAGT | 5663 |
rs781456476 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73186755 | GCACTCCAGTCTGGG[C/T]GACAAAGTGAGACCC | 5663 |
rs781456602 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73199938 | TTTTAGTGGAGACAC[A/G]GTTTCACCATGTTGA | 5663 |
rs781506717 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73196771 | TAAGCCACTGTGCCT[C/G]GCAAGACATGAAATT | 5663 |
rs781509628 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73187989 | GCTGGAGTGCAGTGG[C/T]ATGATCTCGGCTCAC | 5663 |
rs781511032 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73160536 | TGCATAGTGGTTCCA[A/G]TTTCTTCACAACTTT | 5663 |
rs781530411 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73141093 | CCACATCTGCTAAGA[A/T]TGCATTGACCAAAGC | 5663 |
rs781538426 | snp | A/G | 1.6498e-05 | 0.00287206 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217094 | AGCAAAGAGTGACCA[A/G]CTTTTTAATATTTGT | 5663 |
rs781598110 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73159821 | TAACATGGACTACTT[G/T]AGTTTTTTTCTTTTT | 5663 |
rs781599648 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73211231 | TTTTCAAGTAGCCCA[A/G]CTTCCTACTCTACCA | 5663 |
rs781612675 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73168912 | TAGAGCCTGCGCCTG[C/T]CAGAGAGGAGCAACT | 5663 |
rs781616831 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73208071 | GGGGCACCCAGAAGC[C/T]TGGAGATGCCAGGAA | 5663 |
rs781642175 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73146873 | AAACCTTCTGTGAAA[A/T]GGAAGAGTTGAAATC | 5663 |
rs781675066 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73141850 | AGGCTGGCAGATCAC[A/G]AGGTCAGGAGATCGA | 5663 |
rs781707702 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73148339 | TTGAAGCCTTCTCCA[C/G]CTTCCCAAGGTGTGC | 5663 |
rs781753488 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73195209 | ATAGAGTCTCGCTTT[A/G]TTGCCCAGGCTGGAG | 5663 |
rs781779373 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73180340 | CCAGATCTCCACATT[A/T]ACTTGTTCATTTGTG | 5663 |
rs796195803 | snp | C/T | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134740 | TCCATGTTGATCAGG[C/T]TGGTCTCGAACTCCT | 5663 |
rs796272672 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73197620 | GAGTAATCTTTTTAA[C/T]TTGTAGTTCATATCC | 5663 |
rs796273986 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73156669 | AAAAAGTTTTGTTTG[-/T]TTTTTTTTTTTGAGA | 5663 |
rs796355955 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73213141 | AGCCTGTGACTTTCA[C/T]ACTCCTGGAAAAGTA | 5663 |
rs796521224 | in-del | -/ATGTATTACTG | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221478 | ATTTAAATCCATCCT[-/ATGTATTACTG]ATTGTCCTGTGTAGA | 5663 |
rs796521780 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73202735 | CCTCGGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 5663 |
rs796578215 | in-del | -/GG | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73185608 | GGAGAGGGAGACCGT[-/GG]GGGGAGAGAGAGGGA | 5663 |
rs796663872 | in-del | -/TCT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73177289 | TCTCCTTTGCATATC[-/TCT]TCTACTCAGATACCT | 5663 |
rs796671031 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73170181 | TCCTCACCATCTTGG[-/T]TTTGGTGGGTTTTGG | 5663 |
rs796710298 | snp | A/G | | | utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73148008 | AAACAGTATTTCTAT[A/G]CAGTTGCTCCAATGA | 5663 |
rs796748577 | in-del | -/TTT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167829 | CAAGCCTCTTCCACC[-/TTT]TTTTTTTTTTTTTTT | 5663 |
rs796753851 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73200392 | CTCCTCTCTCAGCCT[A/C]CCAAGTAGCTGGAAT | 5663 |
rs796777090 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73193567 | AAAAAAAAAAAAAGC[-/A]AAAAAAAAAAAGCAC | 5663 |
rs796823546 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73171671 | ATTGGCTAATTTAAA[A/G]AGAATGATGGGGTGA | 5663 |
rs796833402 | in-del | -/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194531 | CTGCCAAAGTGTTGG[-/G]ATTACAGGCATGAGC | 5663 |
rs796836842 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73201998 | GTGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 5663 |
rs796848793 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73197853 | TATTTTGTTTATGTT[G/T]TCTCCCCCACCCCCA | 5663 |
rs796902297 | in-del | -/CT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73162448 | TCGCTCGCTCGCGCG[-/CT]CTCTCTCTCTCTCTC | 5663 |
rs796933435 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73166136 | TGAATGTGTATGTTA[A/C]TGTTAAGTTAAACAG | 5663 |
rs796989470 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73192109 | AAAGTTCAGCTTGGG[-/A]AAAAAAAAGTGAATT | 5663 |