SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs661 | snp | A/G/T | 9.88509e-05 | 0.00702963 | PSEN1 | 14 | allele_origin=G(germline)/A(germline) | 14:73217225 | ACACAACCATAGCCT[A/G/T]TTTCGTAGCCATATT | 5663 |
rs7523 | snp | A/G | 0.24932 | 0.249999 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220236 | TAAGGCAGCTCTGTC[A/G]TGGTAGCAGATGGTC | 5663 |
rs14428 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223268 | GAGGCACCCTGCTGC[C/T]CAAGGCTGTGGGAGA | 5663 |
rs165931 | snp | C/T | 0.442113 | 0.159977 | intron-variant | PSEN1 | GRCh38.p7 | 14:73163562 | CTGTTTGTCACTTGA[C/T]TATTCTTAGAATATA | 5663 |
rs165932 | snp | A/C | 0.467238 | 0.123725 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198145 | TACTAATTCAATATC[A/C]TTCTCAAATACTTAC | 5663 |
rs165933 | snp | C/T | 0.35207 | 0.228214 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198646 | TTGCTACTGCCACTA[C/T]CATAATTCAAACCCC | 5663 |
rs165934 | snp | A/C | 0.441158 | 0.161117 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206123 | GTTTTCCTTCTGGTT[A/C]CTTTTCAGGGACTAA | 5663 |
rs165935 | snp | A/G | 0.441977 | 0.16014 | utr-variant-3-prime, downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73220436 | TCTGAGCTACTGTGT[A/G]GCAAAAGCAAAAACA | 5663 |
rs177286 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73184195 | ggggtcagccccccg[C/G]ccggccagccgcccc | 5663 |
rs177412 | snp | A/T | 0.00874735 | 0.0655527 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221080 | CCCAGGATATTTCTT[A/T]TAAGAACCTAACTTC | 5663 |
rs177413 | snp | A/G | 0.297128 | 0.245518 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216486 | gacgtgagccaccac[A/G]catggccTATCATCT | 5663 |
rs177414 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216260 | ccctaggccttaagc[A/G]accagtgatctgctt | 5663 |
rs177415 | snp | A/C | 0.441021 | 0.161279 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211255 | AAGACCAAGCCTATA[A/C]ACTAGTGATGGTAGA | 5663 |
rs177416 | snp | C/T | 0.00253558 | 0.0355156 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206498 | TTTATTAGATAATAT[C/T]TTGATTTTTCAGGGT | 5663 |
rs177417 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205372 | cctgcctcagcctcc[C/T]gagtagctgggacta | 5663 |
rs177418 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | PSEN1 | GRCh38.p7 | 14:73202628 | aaaattagccaggca[C/T]ggtggcgggcgccta | 5663 |
rs183338 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73184180 | gccggccagccgccc[C/T]gtccgggagggaggt | 5663 |
rs184193 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73184146 | ggggtcagccccccg[C/G]ccggccagccgccct | 5663 |
rs184194 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73184107 | gagggaggtgggggg[A/G]tcagccccccgcccg | 5663 |
rs184195 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73184093 | GATCAGCCCCCCGCc[C/T]ggccagccgccccgt | 5663 |
rs214260 | snp | A/G | 0.332337 | 0.236052 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195921 | CGAGATCAGAGTTTA[A/G]Gcttaggcaaataat | 5663 |
rs214261 | snp | A/G | 0.298651 | 0.24522 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195761 | tgggaggctgcttga[A/G]gctaggaggtcaaca | 5663 |
rs214262 | snp | C/T | 0.297382 | 0.245469 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195457 | ggctgggcgcagtgg[C/T]tcaagcctgtaatcc | 5663 |
rs214263 | snp | C/G | 0.332568 | 0.235971 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186207 | TTTTTAGTAGAGACA[C/G]AGTTTCTCCATGTTG | 5663 |
rs214264 | snp | A/C/G | 0.00636936 | 0.0560724 | intron-variant | PSEN1 | GRCh38.p7 | 14:73184543 | caggccagccgccct[A/C/G]tccgagagggaggtg | 5663 |
rs214265 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73184076 | gccagccgccccgtc[C/T]gggagggaggtgggg | 5663 |
rs214266 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73183996 | cctctgcccggccgc[C/T]cctactgggaagtga | 5663 |
rs214267 | snp | C/G | 0.332568 | 0.235971 | intron-variant | PSEN1 | GRCh38.p7 | 14:73180466 | CTCTGGCAAGTTACT[C/G]AATCTCTGACTCAAA | 5663 |
rs214268 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PSEN1 | GRCh38.p7 | 14:73176251 | TTAAAGTGGGGGAGG[C/T]GAATGCTTCCCAGCA | 5663 |
rs214269 | snp | C/T | 0.298651 | 0.24522 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173930 | actcctgggcccaag[C/T]gatcctcctgcctca | 5663 |
rs214270 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | PSEN1 | GRCh38.p7 | 14:73166914 | AAGACCGAGGCTGGC[A/G]TTATAAAGGCATGGT | 5663 |
rs214271 | snp | C/T | 0.299158 | 0.245119 | intron-variant | PSEN1 | GRCh38.p7 | 14:73165962 | ttcaagcaattctcc[C/T]gcgtcagcctcccga | 5663 |
rs214272 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | PSEN1 | GRCh38.p7 | 14:73163850 | ataacaaaatcaaaa[C/G]ttcttaggctcatga | 5663 |
rs214273 | snp | C/T | 0.298398 | 0.245271 | intron-variant | PSEN1 | GRCh38.p7 | 14:73149416 | TGCTGGAGTGGCCTT[C/T]CAGCCTTTTGTGACT | 5663 |
rs214274 | snp | C/G | 0.299158 | 0.245119 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148902 | CTCGTCGCCCAGGCT[C/G]GAGTGCAATGGCGCG | 5663 |
rs214275 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | PSEN1 | GRCh38.p7 | 14:73144546 | GCCTCTTTATAAAAC[G/T]CCAAACCTGCCCCGT | 5663 |
rs214276 | snp | C/T | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73142943 | GGGACAGAATCTACT[C/T]TGGTGTTTTTGCTCT | 5663 |
rs214277 | snp | A/T | 0.100231 | 0.200173 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139288 | gcccagccTTTTTTT[A/T]AAAAAAaaacgaagt | 5663 |
rs214278 | snp | C/T | 0.298651 | 0.24522 | intron-variant | PSEN1 | GRCh38.p7 | 14:73138787 | attttttagtagaga[C/T]ggggtttcaccgtgt | 5663 |
rs214279 | snp | C/G | 0.298144 | 0.245321 | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137870 | tggtctcgaactcct[C/G]agctcaaggatccgc | 5663 |
rs214280 | snp | C/T | 0.0614824 | 0.164198 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134956 | AATCTGATTGCAGTC[C/T]GCTAATATTAATAGG | 5663 |
rs362339 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | PSEN1 | GRCh38.p7 | 14:73147679 | CAGTTAGTTGAAAGT[C/T]GTGACAAATTAATAC | 5663 |
rs362340 | snp | A/G | 0.178465 | 0.239547 | intron-variant | PSEN1 | GRCh38.p7 | 14:73172430 | GGGTTAGGTTTGGCA[A/G]CGTATTATAGAACAA | 5663 |
rs362341 | snp | A/T | 0.21875 | 0.248039 | intron-variant | PSEN1 | GRCh38.p7 | 14:73174750 | TCACACCTTGCCTAA[A/T]CTGGTAGCCACCATG | 5663 |
rs362342 | snp | C/G | 0.149665 | 0.228982 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196049 | ACAGAGCTTTGAGTT[C/G]CTTTTAAACAAAAGA | 5663 |
rs362343 | snp | C/T | 0.179425 | 0.239831 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212852 | AGCATATTTTCCAAC[C/T]AAGTTATTTTTGGTT | 5663 |
rs362344 | snp | C/T | 0.415891 | 0.18703 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223011 | AGTGATCCTTGTGAT[C/T]TTCTCACCTCTTTAA | 5663 |
rs362347 | snp | A/C | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73146606 | ATGTGTAATGATTTG[A/C]ATGATACAAATATAA | 5663 |
rs362348 | snp | C/G | 0.0633504 | 0.166319 | intron-variant | PSEN1 | GRCh38.p7 | 14:73147509 | AATTTGGTCAGCATA[C/G]AAAAAGGAATGTTGA | 5663 |
rs362349 | snp | G/T | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73147606 | TGAAAATGTTTGGTG[G/T]CTCAGGCGGTTCTAC | 5663 |
rs362350 | snp | A/G | 0.162581 | 0.234218 | intron-variant | PSEN1 | GRCh38.p7 | 14:73164384 | AGTTTCATCTGGACA[A/G]TACCCTAAGAGGAGA | 5663 |
rs362351 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | PSEN1 | GRCh38.p7 | 14:73164900 | TAAATTAAATCTGGA[A/C]AGCCAGTGAATCTGC | 5663 |
rs362352 | snp | A/G | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73166249 | TTGGGGACTCTGAAT[A/G]AGCATATGATTGCCC | 5663 |
rs362353 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | PSEN1 | GRCh38.p7 | 14:73166789 | TGATGGGTGGTATAT[A/G]TATTTCTACCTTTTA | 5663 |
rs362354 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | PSEN1 | GRCh38.p7 | 14:73170486 | CTTGGAGCTGCAGCC[A/G]GTAAACAAGTTTTCA | 5663 |
rs362355 | snp | C/T | 0.189576 | 0.242588 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171253 | CTGCAGAAGTATGTT[C/T]CCTGTATGGTATTAC | 5663 |
rs362356 | snp | C/G | 0.0517044 | 0.152246 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171921 | GATTAAGTCCTTCTT[C/G]GTATCTTTTCTCATA | 5663 |
rs362357 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171994 | TTTATTTACATTGTT[C/T]ATTTAATGCCTAATT | 5663 |
rs362358 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73172215 | TGATTCAAATGTCAT[C/G]TAGTTCCATCTCTAC | 5663 |
rs362359 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | PSEN1 | GRCh38.p7 | 14:73172399 | AGGGATTGAAGAATA[C/T]TATCCATATAGGTTA | 5663 |
rs362360 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | PSEN1 | GRCh38.p7 | 14:73172486 | CAGATCTGTCTGCTA[C/T]CTTTCCACAAAGGTG | 5663 |
rs362361 | snp | A/G | 0.10237 | 0.201756 | intron-variant | PSEN1 | GRCh38.p7 | 14:73176351 | TCCCTGCTTTAGTAG[A/G]CTGACCTTGTGACTT | 5663 |
rs362362 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | PSEN1 | GRCh38.p7 | 14:73176911 | ATTCAGTCCTCAGCT[C/G]CCTGAAGTGTGGGTT | 5663 |
rs362363 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | PSEN1 | GRCh38.p7 | 14:73176960 | GGAAACTGCGTATCA[C/T]GTGGTTACCAGTTTT | 5663 |
rs362364 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194073 | CACATTCTGTAACCA[C/T]CAGTGTGACATGGGT | 5663 |
rs362365 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194995 | CTGGTTCTGTTCTTG[C/T]ATTTGAGTAATCAGT | 5663 |
rs362366 | snp | A/T | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195030 | GAACTATAGAAGTCA[A/T]ATACTCTCTCTGACT | 5663 |
rs362367 | snp | C/G | 0.198634 | 0.244666 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198709 | GTAGAATCAATAGTT[C/G]TAGCAACTGAGGAGA | 5663 |
rs362368 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | PSEN1 | GRCh38.p7 | 14:73199180 | GACATTGCTAGCAGA[C/T]GTTTAGAAATGAAAT | 5663 |
rs362369 | snp | C/T | 0.147321 | 0.227941 | intron-variant | PSEN1 | GRCh38.p7 | 14:73203577 | AATCAATAAATAATT[C/T]TTTCATGCATTTTAA | 5663 |
rs362370 | snp | A/C/T | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73203768 | CACTCTGGGAGCTTA[A/C/T]CTAGAAGGGAAACTA | 5663 |
rs362371 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204695 | TACTTGCATAAAGAA[A/G]GAAAACCTAATAAAT | 5663 |
rs362372 | snp | A/T | 0.110872 | 0.20771 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205135 | CATGGATAAAATTAT[A/T]GTGATAAAAAGCCAG | 5663 |
rs362374 | snp | C/T | 0.095934 | 0.196885 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206672 | AATACAGTCAAAGCA[C/T]CCTAGGTTAAGACAC | 5663 |
rs362375 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206926 | GAACCTCTTGTCTAA[C/T]ATGGCCAGAATAACT | 5663 |
rs362376 | snp | C/G | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211458 | ATACCAAGTTACAAC[C/G]CCACAACCTTAGAGC | 5663 |
rs362377 | snp | A/G | 0.125182 | 0.216612 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211505 | cttggtgggattacc[A/G]tgcttggcttggctt | 5663 |
rs362378 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212509 | TTCCAGTAAGCCTTC[A/G]TGGCCGTAATACATT | 5663 |
rs362379 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212775 | GCCACTAAAGCCCTT[A/T]GGTTAGGGCTCAGTC | 5663 |
rs362380 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212993 | AATTATTATGACCTT[A/G]ACATATCCATCAGTT | 5663 |
rs362381 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | PSEN1 | GRCh38.p7 | 14:73213500 | ATGCAAAGTAATAAC[A/G]GACGTGCTTCATCAT | 5663 |
rs362382 | snp | C/T | 0.0101465 | 0.0705004 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217252 | TATTAATTGTAAGTA[C/T]ACACTAATAAGAATG | 5663 |
rs362383 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219471 | TGGAAGGAGGTGCCT[A/G]TAGAAAACGATTTTG | 5663 |
rs362384 | snp | A/C | 0.0858192 | 0.188533 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219602 | CCATCAGCAGCTTGA[A/C]GCGTGGTCACAGGAC | 5663 |
rs362385 | snp | C/T | 0.0414363 | 0.137845 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219653 | CTCTCAGGACTACCG[C/T]TACCAAGAGGTTAGG | 5663 |
rs362387 | snp | A/G | 0.00716266 | 0.059414 | utr-variant-3-prime, downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73220670 | TTTCAGGTTATTCTC[A/G]TCAGCTCCACAAATG | 5663 |
rs362388 | snp | C/T | 0.0444908 | 0.142359 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221719 | TCTTTAAATCATTCA[C/T]CTCAGGCAGAGAACT | 5663 |
rs362389 | snp | A/C | 0.145305 | 0.227022 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222153 | TGTGTTCCTAGAATC[A/C]CAGCTCTGACTCCAA | 5663 |
rs362390 | snp | A/G | 0.0441095 | 0.141807 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222649 | AAAGATGAATAAGAT[A/G]AATTCTCAGAATGTA | 5663 |
rs362391 | snp | A/G | 0.0441095 | 0.141807 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222814 | TTCAGAAATCAATCC[A/G]TTCAGTAAAGTACTC | 5663 |
rs362392 | snp | C/G | 0.0228947 | 0.104514 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222827 | CCATTCAGTAAAGTA[C/G]TCCTTCTCTAAATTT | 5663 |
rs362393 | snp | A/G | 0.111224 | 0.207945 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222921 | ACATTGAATTTGGAA[A/G]GAGACGTGAAAATTG | 5663 |
rs362394 | snp | A/G | 0.0441095 | 0.141807 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223112 | GAGTGTACCAACAAA[A/G]CTGTCATCGGGCTCA | 5663 |
rs362395 | snp | C/T | 0.0185938 | 0.0946107 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223120 | CAACAAAGCTGTCAT[C/T]GGGCTCACAGCTCAG | 5663 |
rs362396 | snp | G/T | 0.0633504 | 0.166319 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223436 | AGTTTCAAAGTCAGC[G/T]GCATATAGTAGCAAG | 5663 |
rs362397 | snp | A/T | 0.00279162 | 0.0372561 | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73223726 | CATGAAAGTATCATA[A/T]TGTATAACTGTAACT | 5663 |
rs362457 | snp | A/G | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143044 | TTGTTCACAGGGCTA[A/G]GAATGTTCATGGCTA | 5663 |
rs362458 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143161 | AGCTGATACTGGACC[A/G]AAATCAAATCTAGCT | 5663 |
rs362459 | snp | G/T | 0.0501905 | 0.150254 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143456 | GTGCAGGCAAAATCT[G/T]TCACCTTTTCTGAGT | 5663 |
rs362460 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143492 | TTTACATGTCAGTAC[A/G]GATTCCTTTCCTCAT | 5663 |
rs405202 | snp | A/C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73151898 | TATATATATATATTT[A/C/T]TTTTTTTTTTTTTTT | 5663 |
rs1000008 | snp | C/T | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73191183 | AATCTGGTCATTTTT[C/T]TTCTTTATAATCTTA | 5663 |
rs1042864 | snp | G/T | 0 | 0 | missense | PSEN1 | GRCh38.p7 | 14:73192710 | CCTGATCTGGAATTT[G/T]GGTGTGGTGGGAATG | 5663 |
rs1057852 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141056 | GCCAACTGCATAAGC[A/G]TAGTTCAAATGTCTG | 5663 |
rs1203310 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73138837 | tgggactacaggcgc[C/G]cgccatcacgcccgg | 5663 |
rs1203311 | snp | A/G/T | 0.143284 | 0.226079 | intron-variant | PSEN1 | GRCh38.p7 | 14:73138823 | cccgccatcacgccc[A/G/T]gctaatttttttttt | 5663 |
rs1639669 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73138903 | ctccgctcactgcaa[C/G]ctccttctcccgggt | 5663 |
rs1735120 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73138897 | gcgtgaacccgggag[A/G]cggagcttgcagtga | 5663 |
rs1735121 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73152563 | agtgagctgagattg[A/T]gccactgcaccccag | 5663 |
rs1800839 | snp | C/T | 0.0517044 | 0.152246 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136423 | GCCGGCCGCCAACGA[C/T]GCCAGAGCCGGAAAT | 5663 |
rs1800840 | snp | A/G | 0.415235 | 0.18761 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134682 | GGCATGCGCCACCAC[A/G]CCTGGCTAACTTTTT | 5663 |
rs1800844 | snp | C/G | 0.327445 | 0.237702 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73136992 | TTGTCCAGGGGCGAC[C/G]AGCATTCTGGGCGAA | 5663 |
rs2272585 | snp | G/T | 0.185155 | 0.241444 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216933 | AAGACTCCAGAGTCA[G/T]TCACATAGAATCTGG | 5663 |
rs2280791 | snp | C/T | 0.417034 | 0.18601 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208242 | GCCCTGTTTGTCTTA[C/T]GGTTCTTTCAATCCT | 5663 |
rs2283427 | snp | A/T | 0.235273 | 0.249566 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168791 | GGAGAGGGCAGGGGC[A/T]GCCACCCTGACCCTC | 5663 |
rs2333030 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179230 | TCTTCCAGTCAGAGT[A/G]AGGATTCCCTCCCTC | 5663 |
rs2735781 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73202462 | tatatatatatatat[A/T]ttttttttttttttt | 5663 |
rs2735783 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73138508 | acaggcgtgagccac[C/T]ctgcccggccGGCTA | 5663 |
rs2738226 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73138454 | tcgatctcctgacct[C/G]gtgatccgcccgcct | 5663 |
rs3025773 | snp | A/G | 0.0879971 | 0.190408 | intron-variant | PSEN1 | GRCh38.p7 | 14:73142299 | TAAAGAATAAATCAC[A/G]AGCTCATTGGCACTT | 5663 |
rs3025774 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143556 | TGTGAAAAGAACTTT[C/G]AAGATAGTATTGGAA | 5663 |
rs3025776 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148548 | GATTCAGGAAAAGAA[C/T]GTAATCTGTGCTGTC | 5663 |
rs3025777 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | PSEN1 | GRCh38.p7 | 14:73163447 | TCACAAACAATCTTA[C/T]AGGAGTCATTCATTA | 5663 |
rs3025778 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PSEN1 | GRCh38.p7 | 14:73163631 | TAAAACCAGATCAAC[A/G]TAGAGAAAGGCTTCC | 5663 |
rs3025779 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | PSEN1 | GRCh38.p7 | 14:73163706 | TGAGTGACAAGGAAC[A/G]GTCAGGTGGGAGAAG | 5663 |
rs3025780 | snp | G/T | 0.235564 | 0.249583 | intron-variant | PSEN1 | GRCh38.p7 | 14:73167758 | TTTTTTTTTTTGTCT[G/T]CATTTCTGGTGGGGT | 5663 |
rs3025781 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173170 | AGAGGCACTAATTAT[A/G]AGCCATATTACCTTT | 5663 |
rs3025782 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | PSEN1 | GRCh38.p7 | 14:73177010 | GACCTTTTTGAACCT[A/G]ATTTTTTCTGGACCT | 5663 |
rs3025783 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196100 | AGAGTAGTGATTCTC[A/G]GCTCCATTTTTACAA | 5663 |
rs3025784 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197636 | TTGTAGTTCATATCC[A/G]TGATTAGTTTAGAAG | 5663 |
rs3025785 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197833 | ACAGATGTTCTGTGT[C/T]ATTTTATTTTGTTTA | 5663 |
rs3025786 | snp | C/T | 0.0847223 | 0.187572 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198010 | TTTTATTAGATGTCT[C/T]TTATGTTTTTCTTTT | 5663 |
rs3025787 | snp | C/G | 0.148326 | 0.228391 | intron-variant | PSEN1 | GRCh38.p7 | 14:73213398 | TGTCCTCCTCCTCTT[C/G]GTCTCCAACTTTTAA | 5663 |
rs3025788 | snp | A/G | 0.0448719 | 0.142907 | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73224069 | AGCCCCAAAGCAGCT[A/G]TCCTTAATACATCCT | 5663 |
rs3025789 | snp | C/T | 0.0441095 | 0.141807 | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73224106 | TATTTTTTCTAATAA[C/T]TTTCACATTAATGTA | 5663 |
rs3182301 | snp | A/C | 0 | 0 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219337 | TTCTTTGACTATAAC[A/C]AAATCTGGGGAGGAC | 5663 |
rs4899458 | snp | A/C | 0.0898077 | 0.191933 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181493 | gccaggtgcagtggc[A/C]cggacctgtagaccc | 5663 |
rs7143491 | snp | A/C | 0.0437281 | 0.141251 | intron-variant | PSEN1 | GRCh38.p7 | 14:73213259 | CTCTTCTACTTTCCT[A/C]TTTTCTCACAGGCAC | 5663 |
rs7145968 | snp | G/T | 0.166506 | 0.235645 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141839 | ttgggaggcagaggc[G/T]ggcagatcacgaggt | 5663 |
rs7147079 | snp | A/G | 0.185155 | 0.241444 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217833 | gacggagtctctgtc[A/G]cccaggctggagtgg | 5663 |
rs7147896 | snp | C/G | 0.021333 | 0.101051 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198833 | ggatggagtacagta[C/G]tgtgatcatggctca | 5663 |
rs7148656 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217864 | tgcaatctcggctca[C/T]tgcaacctctgcctc | 5663 |
rs7152131 | snp | A/C | 0.142609 | 0.225759 | intron-variant | PSEN1 | GRCh38.p7 | 14:73190472 | AGGGTGACAGTCAGA[A/C]CTTGTCTCTATTTAA | 5663 |
rs7153378 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169525 | CTTCTCTCTTCCAGC[C/T]TGTTTATCTTATTGT | 5663 |
rs7154061 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | PSEN1 | GRCh38.p7 | 14:73199832 | CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG | 5663 |
rs7154168 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73175212 | gctcactgcaagctg[G/T]gcctcctgggttcaa | 5663 |
rs7154312 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169336 | TTCTCTCCTTGGTCA[G/T]CTTTTTACTGTATTT | 5663 |
rs7156668 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187980 | gttgcccaggctgga[A/G]tgcagtggcatgatc | 5663 |
rs7158911 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PSEN1 | GRCh38.p7 | 14:73184603 | gcggccgggcagagg[C/T]gcccctcacctcccg | 5663 |
rs7159873 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200636 | AAAAATAAATTTCAC[A/G]GTAACTATCATCTCT | 5663 |
rs7160427 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193922 | ttggcctctcaaggt[A/G]ttgggattataggtg | 5663 |
rs7161030 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200729 | TTTTTTGCCAATTTT[C/T]CTGTTGAGTTACTGG | 5663 |
rs7161398 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200929 | ggtggtgcacacttg[C/T]aatcccagttacttg | 5663 |
rs7359038 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | PSEN1 | GRCh38.p7 | 14:73142079 | ctcaaaaaaaaaaaa[A/G]agaaaagaaaCTACA | 5663 |
rs8006221 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | PSEN1 | GRCh38.p7 | 14:73146433 | ctggccttaagcTCT[C/T]TATTTTTTAAGCAAA | 5663 |
rs8006497 | snp | A/G | 0.144296 | 0.226554 | intron-variant | PSEN1 | GRCh38.p7 | 14:73163024 | GTACTTTTTTTGAAG[A/G]GCTCTATTTTTATTT | 5663 |
rs8008686 | snp | A/G | 0.184838 | 0.241358 | intron-variant | PSEN1 | GRCh38.p7 | 14:73150808 | ggtgcggtggctcac[A/G]cctgtaatcccaaca | 5663 |
rs8011335 | snp | A/T | 0.211819 | 0.247067 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160197 | TTTTGCTTAGCATAA[A/T]GTCCTCAAGGTTCAT | 5663 |
rs8011748 | snp | A/G | 0.186737 | 0.241863 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186275 | TCCCAGCTACTTGGG[A/G]GGCTGAGGCAGGAGA | 5663 |
rs8018725 | snp | C/T | 0.281049 | 0.248064 | intron-variant | PSEN1 | GRCh38.p7 | 14:73149020 | GTGAGACAGTTGGAG[C/T]ATCTATAGGATTTTT | 5663 |
rs8018739 | snp | C/T | 0.221141 | 0.248329 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196663 | tatttttggtagaga[C/T]ggggttttgccatct | 5663 |
rs8020594 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | PSEN1 | GRCh38.p7 | 14:73161596 | caggagacaccccag[A/G]ctcaagctgtcaata | 5663 |
rs8021006 | snp | A/T | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73175733 | agtgtttcactattt[A/T]aaaaaacagtaatat | 5663 |
rs8023183 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179447 | cacagtgaaaacctg[C/T]ctctactaaaataca | 5663 |
rs9743635 | snp | A/T | 0.19459 | 0.243782 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169735 | actgcagcctccacc[A/T]cccaggttcaggtga | 5663 |
rs10130116 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216542 | aaggtgggtggatca[C/T]gaggtcaggagttcg | 5663 |
rs10131037 | snp | C/G | 0.0341408 | 0.126114 | intron-variant | PSEN1 | GRCh38.p7 | 14:73185591 | gagaccgtggaaaga[C/G]agggagagggagacc | 5663 |
rs10131356 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210284 | TGCTCAAAAAAGCAA[A/G]TGTAATTATAGTATA | 5663 |
rs10131938 | snp | G/T | 0.0441095 | 0.141807 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194439 | ttaaaaaaaaatttt[G/T]tttcagagatgagat | 5663 |
rs10132644 | snp | C/G | 0.0441095 | 0.141807 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204111 | tcaagcaattctcct[C/G]cctcagcctcccgag | 5663 |
rs10134564 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | PSEN1 | GRCh38.p7 | 14:73214518 | ctgggcaacaagagc[A/G]aaactccatctcaaa | 5663 |
rs10134874 | snp | C/T | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73178220 | caccacacccggccc[C/T]ttttttttttttttt | 5663 |
rs10135273 | snp | C/T | 0.0898077 | 0.191933 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151684 | gtgatcctgccacct[C/T]agcctcccaagtagc | 5663 |
rs10136281 | snp | A/T | 0.0444908 | 0.142359 | intron-variant | PSEN1 | GRCh38.p7 | 14:73190543 | TCAAGTAGAAAAGTA[A/T]ATATATGACATGTAT | 5663 |
rs10136911 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | PSEN1 | GRCh38.p7 | 14:73153829 | gcgattctcctgcct[C/T]agtctcccgagtagt | 5663 |
rs10140990 | snp | C/G | 0.180064 | 0.240019 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216418 | caatcattgaatcat[C/G]tcttccagttttatg | 5663 |
rs10141217 | snp | A/T | 0.424037 | 0.179474 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179996 | ATTTTATTTTATTTT[A/T]TTTTTTGAGACGGAG | 5663 |
rs10142471 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | PSEN1 | GRCh38.p7 | 14:73207116 | gagctaaggagttcc[A/G]gattaccctgggcaa | 5663 |
rs10142485 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73147068 | TTTTTTTTctgcaac[C/T]tccacctcctgggtt | 5663 |
rs10143618 | snp | C/T | 0.0441095 | 0.141807 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73220979 | CCAGCTTTTTCTTCT[C/T]TTGCCTGCTGTTTTC | 5663 |
rs10143704 | snp | A/T | 0.0901694 | 0.192235 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156055 | catttaaaaataTTT[A/T]ATggcttggtggctc | 5663 |
rs10145927 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | PSEN1 | GRCh38.p7 | 14:73172573 | CTCCTTGGTTTATAC[A/G]TTGTCTGTGGCTGCT | 5663 |
rs10146467 | snp | G/T | 0.179744 | 0.239925 | intron-variant | PSEN1 | GRCh38.p7 | 14:73214389 | tacaaaattagccca[G/T]tgtggtggcacatgc | 5663 |
rs10146743 | snp | G/T | 0.184838 | 0.241358 | intron-variant | PSEN1 | GRCh38.p7 | 14:73214673 | tgaataaatcttgag[G/T]actttgtgctaagtg | 5663 |
rs10147873 | snp | C/T | 0.198634 | 0.244666 | intron-variant | PSEN1 | GRCh38.p7 | 14:73153962 | caagtgatctgacca[C/T]ctaggcctctcaaag | 5663 |
rs10148612 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | PSEN1 | GRCh38.p7 | 14:73209040 | cccgcacacccggcc[A/G]ggtcatgacagcacc | 5663 |
rs10151436 | snp | A/T | 0.312104 | 0.242163 | intron-variant | PSEN1 | GRCh38.p7 | 14:73149387 | taggcttgtgtgtac[A/T]tttcactacaaacag | 5663 |
rs10564849 | in-del | -/CAG | 0.29789 | 0.24537 | intron-variant | PSEN1 | GRCh38.p7 | 14:73167148 | AAGAGTATATGGTAC[-/CAG]CAGCACCTGATTATG | 5663 |
rs10701455 | in-del | -/TGTTTT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73177391 | TTTTGTTTTTGTTTT[-/TGTTTT]GAGATAAAGTCTTGC | 5663 |
rs11379162 | in-del | -/C | 0.263535 | 0.249633 | intron-variant | PSEN1 | GRCh38.p7 | 14:73175314 | TATTTTTAGTAGAGA[-/C]CTGGGTTTTACCGTG | 5663 |
rs11552351 | snp | C/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219597 | GTGCCCCATCAGCAG[C/T]TTGACGCGTGGTCAC | 5663 |
rs11623963 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73215389 | tggagtttgagacca[A/G]cctggccaacatggt | 5663 |
rs11626604 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73204006 | tatttattttttatt[G/T]tatttttttgagaca | 5663 |
rs11848943 | snp | A/T | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134532 | tttatttatttattt[A/T]tttttattttttgag | 5663 |
rs11850179 | snp | G/T | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135429 | ttgctctgtctccca[G/T]gctggagtgcagtgg | 5663 |
rs12184969 | snp | C/T | 0.223225 | 0.248562 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186335 | GGTGAGCCGAGATTG[C/T]GCCATTGCACTCCAT | 5663 |
rs12323830 | snp | A/T | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151896 | tatatatatatatat[A/T]ttttttttttttttt | 5663 |
rs12432944 | snp | A/T | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73202464 | tatatatatatatat[A/T]ttttttttttttttt | 5663 |
rs12432960 | snp | A/G | 0.160609 | 0.233472 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204251 | GATCCACCCACCTCC[A/G]ACTCCCAAAGTGCTG | 5663 |
rs12433115 | snp | G/T | 0.21875 | 0.248039 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204805 | actttgggaggctga[G/T]gcgggaggattgctt | 5663 |
rs12435869 | snp | A/G | 0.147321 | 0.227941 | intron-variant | PSEN1 | GRCh38.p7 | 14:73202829 | TTAGCAGCACATAAT[A/G]GTAAAATTGGAATGA | 5663 |
rs12586604 | snp | C/G/T | 0.105366 | 0.204441 | intron-variant | PSEN1 | GRCh38.p7 | 14:73146946 | GGAATGTGGCCCCCC[C/G/T]AGGAGGGTGAACTCT | 5663 |
rs12587333 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181441 | aaactccatctcaaa[A/G]tcaatcaatcaatca | 5663 |
rs12587379 | snp | A/G | 0.116838 | 0.211584 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204474 | TGCTTGAAGCCAAAT[A/G]TGGCCCATGGCTTGT | 5663 |
rs12587473 | snp | C/T | 0.10237 | 0.201756 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195660 | GAAGTGGCACGATTA[C/T]AGCTCACTGTAGCTT | 5663 |
rs12588591 | snp | C/T | 0.320575 | 0.239832 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158659 | agaagatggagtctt[C/T]ctatgtttcacaggc | 5663 |
rs12878362 | snp | A/C | 0.253824 | 0.249971 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158834 | tacatttctaccagc[A/C]gtatgagttccagtt | 5663 |
rs12882076 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73180272 | ctacaggcctgagcc[A/C]ccacgcccagccTTA | 5663 |
rs12882210 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73180265 | gctgggactacaggc[C/G]tgagccaccacgccc | 5663 |
rs12882830 | snp | A/G | 0.225893 | 0.248835 | intron-variant | PSEN1 | GRCh38.p7 | 14:73180525 | TTCATATCAGTGGTT[A/G]GTTATGCAATGTCTG | 5663 |
rs12883075 | snp | C/T | 0.254385 | 0.249962 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156000 | gttatgtgggaactc[C/T]gtgtactttctgctc | 5663 |
rs12884515 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73138382 | cgccaccacgcccgg[A/C]taatttttttgtatt | 5663 |
rs12885237 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73218171 | agctcactgcaactt[C/G]tgcctcctaggttca | 5663 |
rs12890801 | snp | G/T | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205076 | CAGCTTCTTTGATTG[G/T]GTGTTTCTTTCATAA | 5663 |
rs12894420 | snp | A/G | 0.242488 | 0.249887 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205411 | GTGAACCCAGGAGAC[A/G]GAGCTTGCAGTGAGC | 5663 |
rs12896793 | snp | A/G | 0.252983 | 0.249982 | intron-variant | PSEN1 | GRCh38.p7 | 14:73209334 | CGCTGCTGCCATCAA[A/G]ACCACTAGTAAACCT | 5663 |
rs13379148 | snp | C/T | 0.162909 | 0.23434 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204321 | tttttttaatttaaa[C/T]GAAATCTGCTTATTT | 5663 |
rs17124867 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151372 | TTGCTGTGATTGGAT[A/G]TATGGATCTTAGAAC | 5663 |
rs17124882 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | PSEN1 | GRCh38.p7 | 14:73155089 | ATAAAAATATTACCA[C/T]AGAAGTGCCAAGAAT | 5663 |
rs17125150 | snp | A/C/G | 0.0345262 | 0.126772 | intron-variant | PSEN1 | GRCh38.p7 | 14:73172243 | TACGACTCTCATGGG[A/C/G]TCCAAAGAAGAGTTT | 5663 |
rs17125152 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | PSEN1 | GRCh38.p7 | 14:73172360 | CATCTAAGACAGCAG[A/G]TGAAGGGCAGGGGTT | 5663 |
rs17125457 | snp | C/T | 0.327914 | 0.237549 | intron-variant | PSEN1 | GRCh38.p7 | 14:73191429 | TGATGATTCTTCTCC[C/T]GCTTTGAAGGTGAAA | 5663 |
rs17125555 | snp | G/T | 0.187369 | 0.242028 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197238 | GCGCCCGGCCTATAT[G/T]CTGAATTTTCATGAC | 5663 |
rs17125721 | snp | A/G | 0.030139 | 0.119001 | PSEN1 | 14 | allele_origin=G(unknown)/A(germline) | 14:73206470 | CCAAGTATAATGCAG[A/G]AAGTAGGTAACTTTT | 5663 |
rs17125952 | snp | A/G | 0.0345262 | 0.126772 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223178 | GTCCTCTCCTCTAAC[A/G]GGAAACACCTCAGAT | 5663 |
rs17182181 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73191291 | ACTTTGCATAAATGG[G/T]ATCATAAATGGGATC | 5663 |
rs17408630 | snp | A/G | 0.415235 | 0.18761 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193584 | AAAAAAAAAAGCACA[A/G]GCAGAGTGGTAGACA | 5663 |
rs17781788 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | PSEN1 | GRCh38.p7 | 14:73140063 | ATTTTGAATAATCAT[A/G]TCTCCCTTATAGAGT | 5663 |
rs17781801 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | PSEN1 | GRCh38.p7 | 14:73149927 | AGCAAATACTGTGAC[A/G]AGCTGCTATAGCCTG | 5663 |
rs17781809 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154207 | TATACCTGTGTGTAT[A/G]TATTGAAAAACGTTA | 5663 |
rs17781841 | snp | G/T | 0.0528381 | 0.153711 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216815 | TATCTCAGAATTCTT[G/T]TAAGGATTTCTTAGT | 5663 |
rs28431180 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181461 | TCAATCAATCAGTCA[A/G]TCAATCATAGTTTCA | 5663 |
rs28451346 | snp | A/T | 0.185155 | 0.241444 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194425 | CCATGCCTAATTTTT[A/T]AAAAAAAAATTTTTT | 5663 |
rs28482166 | snp | C/T | 0.189261 | 0.242509 | intron-variant | PSEN1 | GRCh38.p7 | 14:73202418 | AATATCTATCACATA[C/T]TATATATATATATAT | 5663 |
rs28506983 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73185477 | GCGTGAGTCTGCAAT[C/T]GCAGGCACTCGGCAG | 5663 |
rs28532025 | snp | A/G | 0.0898077 | 0.191933 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208995 | GGGCCAAGGTGGCAG[A/G]GGGCTGGCATGTCAG | 5663 |
rs28607501 | snp | G/T | 0.284733 | 0.247575 | intron-variant | PSEN1 | GRCh38.p7 | 14:73207750 | CAGCCTAGCTGGCTA[G/T]GCTTGGCTTTCTCTA | 5663 |
rs28613010 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201248 | ACACGCCGCCACGCC[C/T]GGCTAATTTTTGTAT | 5663 |
rs28660183 | snp | A/G | 0.179744 | 0.239925 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212167 | CCAGGTTGGAGTGCA[A/G]TGGTGCGATCTTGGC | 5663 |
rs28713521 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201240 | CTACAGGCACACGCC[A/G]CCACGCCCGGCTAAT | 5663 |
rs28719583 | snp | A/G | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169313 | TTAAGCTTAGGGGTT[A/G]TTTACACTTCTCTCC | 5663 |
rs33930642 | in-del | -/A | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154434 | CGATCTTGTCTCTAC[-/A]AAAAAAAAAAAGTGA | 5663 |
rs34006824 | in-del | -/AAT/AATAAT/T | 0.446132 | 0.167135 | intron-variant | PSEN1 | GRCh38.p7 | 14:73166049 | AGACTCTGTCTCCAA[-/AAT/AATAAT/T]AATAATAATAATAAT | 5663 |
rs34023728 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73178219 | CACCACACCCGGCCC[-/T]TTTTTTTTTTTTTTT | 5663 |
rs34048372 | in-del | -/T/TT | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160803 | TTTAATTGTAGGACT[-/T/TT]TTTTTTTTTTTTTTT | 5663 |
rs34062286 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73163871 | ATTTTGTTATGAGCA[-/T]GACAAGAAGCCATTG | 5663 |
rs34069665 | in-del | -/AA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73166047 | TGAGACTCTGTCTCC[-/AA]AAAATAATAATAATA | 5663 |
rs34086577 | snp | C/G | 0.00597247 | 0.0543191 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136191 | ATTTAGGATGGCCAT[C/G]GCTTGTATGCCGGGA | 5663 |
rs34138587 | in-del | -/A | 0 | 0 | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73223938 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAGTTT | 5663 |
rs34194809 | in-del | -/T | 0.499994 | 0.00179711 | intron-variant | PSEN1 | GRCh38.p7 | 14:73183293 | TGGCTAATTTTTGTA[-/T]TTTTTTTTTTTAATT | 5663 |
rs34291816 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73209071 | AGCCTCAGCCACAAC[-/T]TTTGCTCTGAAATCG | 5663 |
rs34315326 | in-del | -/T | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194585 | TGCCTGGCCATACAC[-/T]TTTTTTTTTTTTTTT | 5663 |
rs34365321 | in-del | -/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73170662 | TTAAACTGCATACTT[-/C]CCTGTACATTGTTTT | 5663 |
rs34369135 | in-del | -/T | 0.488965 | 0.0734569 | intron-variant | PSEN1 | GRCh38.p7 | 14:73153662 | ATATCCATTAAGTCA[-/T]TTTTTTTTTTTTTTG | 5663 |
rs34420638 | in-del | -/AGC | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167149 | AGAGTATATGGTACC[-/AGC]AGCACCTGATTATGC | 5663 |
rs34450796 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194603 | GACGGAGTCTGGCTC[-/T]TGTCGCCCAGACTGG | 5663 |
rs34456935 | in-del | -/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73163349 | CGGGAGGCCAAGGCA[-/G]GGAGGATTGCTTGAG | 5663 |
rs34514951 | in-del | -/T/TT | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217796 | TTTCAAAACTATGAT[-/T/TT]TTTTTTTTTTTTTTT | 5663 |
rs34528538 | in-del | -/A | 0.329317 | 0.237084 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204529 | ATGCTTTTTACATTT[-/A]AAAAAAAAAAAAAAG | 5663 |
rs34545469 | in-del | -/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73174029 | GTATTTTATATGCAT[-/G]GGAATCTATATGTCA | 5663 |
rs34558745 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73196426 | TACTATATTATATTG[G/T]ACATATATATTATTA | 5663 |
rs34576363 | in-del | -/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73170421 | TAAGGTAAGATAGTT[-/C]CCTTGCATATGTGGT | 5663 |
rs34601398 | in-del | -/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73155760 | TGGGCTCAAGCGATT[-/C]CTCCCGTCTCGGCCT | 5663 |
rs34623110 | snp | A/G | 0.0970103 | 0.197722 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148358 | CCCAAGGTGTGCAGC[A/G]CCTCATAGTTCATGT | 5663 |
rs34667801 | in-del | -/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73155039 | CTAACCTAATCTGAT[-/G]CTCACCTAGCATTTC | 5663 |
rs34669034 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167829 | CAAGCCTCTTCCACC[-/T]TTTTTTTTTTTTTTT | 5663 |
rs34683189 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73168156 | GGTCAGGAGTTCAAG[-/A]ACCAGCCTGGCCAAC | 5663 |
rs34700665 | in-del | -/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73147273 | CAGGCATGAGCCACC[-/G]GCTCCTGGCTGAGTC | 5663 |
rs34773764 | in-del | -/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73171959 | TCCTTTCTCACTTGT[-/C]CACAATTTGCAAATA | 5663 |
rs34815990 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73158611 | CAGGCGTGAGCCATC[-/A]ACACCTGGCCAGTTT | 5663 |
rs34823740 | in-del | -/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73140906 | CTCAGGGCTCTGCTT[-/C]CCTTGTAGGTAGATG | 5663 |
rs34826717 | in-del | -/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73205698 | AAATTTCCCTCCAGT[-/G]GGGGATTATACCATT | 5663 |
rs34940341 | in-del | -/T | 0.134802 | 0.221877 | intron-variant | PSEN1 | GRCh38.p7 | 14:73177012 | CCTTTTTGAACCTAA[-/T]TTTTTCTGGACCTTA | 5663 |
rs34989261 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73155966 | TGGTGCAGGATGTTG[-/A]ATAGAGGCTGTTGGA | 5663 |
rs34992040 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73205491 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 5663 |
rs35050681 | in-del | -/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167542 | CTAAAGGCCTCACCT[-/C]CTTGATACTACCACA | 5663 |
rs35093253 | in-del | -/T | 0.466204 | 0.125522 | intron-variant | PSEN1 | GRCh38.p7 | 14:73202211 | GCTAATTTTTTTTTT[-/T]CCATATTTTTAGTTG | 5663 |
rs35152004 | in-del | -/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73174600 | GACCTTTATGAATCT[-/G]CCTCATTCACAAATA | 5663 |
rs35223948 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73140203 | CTTTTTTTGCTATTC[-/T]TTTTTTTTTTTTTTT | 5663 |
rs35230037 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194425 | CATGCCTAATTTTTT[-/A]AAAAAAAAATTTTTT | 5663 |
rs35294154 | in-del | -/T | 0.243633 | 0.249919 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196475 | CTTTGAGGCATGAAA[-/T]TTTTTTTTTTTTTTT | 5663 |
rs35364450 | in-del | -/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73204754 | GGAAATCCATAAACA[-/G]GGCTGGGTGCAGTGG | 5663 |
rs35383831 | in-del | -/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73206928 | CCTCTTGTCTAACAT[-/G]GGCCAGAATAACTGA | 5663 |
rs35472128 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73139860 | TGGATGAGAGTGAGG[-/A]AAAAGGTATTAGTAT | 5663 |
rs35515618 | in-del | -/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167691 | TTCAGTCTACACTGT[-/G]GACATGATAGGTATG | 5663 |
rs35573180 | in-del | -/CT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73162447 | TCGCTCGCTCGCGCG[-/CT]CTCTCTCTCTCTCTC | 5663 |
rs35581508 | snp | A/G | 0.224412 | 0.248687 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139378 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTCGCCA | 5663 |
rs35601589 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73211140 | AGAAGAAATTTATTC[-/T]TTTCACGTGACAGGA | 5663 |
rs35614354 | in-del | -/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73144543 | CTACGGGGCAGGTTT[-/G]GGAGTTTTATAAAGA | 5663 |
rs35615325 | in-del | -/T | 0.426813 | 0.17674 | intron-variant | PSEN1 | GRCh38.p7 | 14:73159180 | TTTTTGAAGGGCAGA[-/T]TTTTTTTTTTTTTTT | 5663 |
rs35632933 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73150600 | AACCCTGTCTCTACT[-/A]AAAAAAAATGCAAAA | 5663 |
rs35642104 | in-del | -/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73216583 | ACCAACATGGTGAAA[-/C]CCCTGTCTCCATCAA | 5663 |
rs35643620 | in-del | -/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73156167 | GGTGAAACCCCATCT[-/C]CTATGAAATAAAAAA | 5663 |
rs35671551 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73173444 | ATTGGTGAGTTGGGG[-/A]AAAAGTGACTTATAA | 5663 |
rs35684204 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222613 | TTCTGTGTTCCCGTA[A/G]GTTCTGGAGTCTGAG | 5663 |
rs35710852 | in-del | -/C | 0.0479149 | 0.147179 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168090 | CTGGGTGCGGTGGCT[-/C]CACTCCTATAATCCC | 5663 |
rs35747435 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73150765 | GTAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 5663 |
rs35891140 | snp | A/G | 0.223522 | 0.248594 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145185 | GGCATGAGCCACTGC[A/G]TCCGGCCTACTTACC | 5663 |
rs35983175 | in-del | -/T | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73147061 | TTTTTTTTTTTTTTT[-/T]CTGCAACCTCCACCT | 5663 |
rs36008515 | in-del | -/A | 0.190519 | 0.242821 | intron-variant | PSEN1 | GRCh38.p7 | 14:73180015 | TTGAGACGGAGTCTC[-/A]AGTCTCTCGCCCAGG | 5663 |
rs36023515 | in-del | -/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73174607 | ATGAATCTCCTCATT[-/G]CACAAATAACACTGT | 5663 |
rs41345849 | snp | C/G | | | missense | PSEN1 | GRCh38.p7 | 14:73173634 | ACTCAATTCTGAATG[C/G]TGCCATCATGATCAG | 5663 |
rs45456295 | snp | C/G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73174267 | AGGGCCTTGCCCTGT[C/G/T]ACCCAGGCTGGAGTG | 5663 |
rs45511501 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73137128 | CTTCCCTCTCAGATT[C/G/T]TTCTCACCGTTGTGG | 5663 |
rs55657666 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | PSEN1 | GRCh38.p7 | 14:73183158 | AGTCTCGCTCTGTTG[C/T]TCAGGCTGGAGTGCA | 5663 |
rs55709619 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73200817 | GCACTTTGGGAGGCC[G/T]AGGTGGGCGGATCAC | 5663 |
rs55730237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73218890 | TTATTTTCAGATTCT[A/G]TTTCTTTACTAGAAT | 5663 |
rs55812918 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216231 | TCTAGAAAAGGCAAA[C/T]TTATTGAGATAGAAA | 5663 |
rs55850750 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139890 | TTGGCTTTTCACAAC[A/G]CCTTGTACGGTTTCT | 5663 |
rs55853751 | in-del | -/G | 0.151334 | 0.229706 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194529 | GCCTGCCAAAGTGTT[-/G]GGATTACAGGCATGA | 5663 |
rs55975913 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194613 | TGGCTCTGTCGCCCA[A/G]ACTGGAGTGCAGTGG | 5663 |
rs56008848 | snp | A/G | 0.253264 | 0.249979 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201079 | AGAGAATATCTTTTT[A/G]TTTGTTTGTTTGTTT | 5663 |
rs56121216 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73139182 | CAGCTACTCGGGAGG[C/G]TGAGGCAGGACAATG | 5663 |
rs56240305 | in-del | -/CTATCTAT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73158328 | TATCTATCTATCTAT[-/CTATCTAT]TTTTAAGACGGAGTT | 5663 |
rs56349203 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73177378 | ACTGCTTTGCTGGGG[G/T]TTTTTTGTGTGTGTG | 5663 |
rs56381527 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73154435 | CTTGTCTCTACAAAA[-/A]AAAAAAGTGAAAATT | 5663 |
rs56383209 | in-del | -/TC | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162464 | CTCTCTCTCTCTCTC[-/TC]CATGAGAAGGAGAGA | 5663 |
rs56754992 | in-del | -/TTT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73151927 | TTTTTTTTTTTTTTT[-/TTT]GAGACGGAGTCTCGC | 5663 |
rs57050244 | snp | C/T | 0.135825 | 0.222405 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162920 | GTACTCTATACCTTT[C/T]AATACTTTCTTTGAG | 5663 |
rs57196093 | in-del | -/CTAT/TCTA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73158283 | TATCTATCTATCTAT[-/CTAT/TCTA]TTTTAAGACGGAGTT | 5663 |
rs57307382 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212885 | CTTGTTTTTGCAAGA[A/G]TGAAACTTGATTAAA | 5663 |
rs57524406 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73162016 | AAAAAAAAAAAAAAA[-/A]TAGAAAAAGAAACCA | 5663 |
rs57815955 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | PSEN1 | GRCh38.p7 | 14:73146231 | TCTCACTCTGTTGCC[C/T]AGGCTGAGTACAGTG | 5663 |
rs57895054 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186548 | TTGGGAGTCTGAGGC[A/G]GGCGGATCACTTGAG | 5663 |
rs58317194 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217511 | ATTCCCCAGGAAATT[A/C/T]TGGTATTTCTGTTTA | 5663 |
rs58458484 | snp | C/T | 0.162581 | 0.234218 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151046 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC | 5663 |
rs58497887 | in-del | -/A | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73216772 | TCAAAAAAAAAAAAA[-/A]TATTAATTAATATGA | 5663 |
rs58637970 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73218108 | TTTTTTTTTTTTTTT[-/T]GGAGACAGAGTCTTG | 5663 |
rs59013584 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167852 | TTTTTTTTTTGCTTC[A/G]AAGAATGATTGCCTT | 5663 |
rs59194960 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | PSEN1 | GRCh38.p7 | 14:73155875 | AAACCCATAGACTGT[A/G]TAACACCAAAAAGTG | 5663 |
rs59341951 | snp | A/G | 0.416871 | 0.186156 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205421 | GAGACGGAGCTTGCA[A/G]TGAGCCGAGATCATG | 5663 |
rs59962242 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | PSEN1 | GRCh38.p7 | 14:73175511 | ACTTTCCAAATGTAG[A/G]AGTCTACTCTGTTTC | 5663 |
rs59966121 | snp | A/T | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223047 | CACAACACAAGAGAT[A/T]AAAAACAGAGGTTTC | 5663 |
rs60208626 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | PSEN1 | GRCh38.p7 | 14:73218190 | CTCCTAGGTTCAAGC[A/G]ATCCTCCTGTCTCAG | 5663 |
rs60308291 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151465 | GGCTGTATTACATCT[A/G]TCTCAGAAAAATAAG | 5663 |
rs60320273 | snp | C/T | 0.162581 | 0.234218 | intron-variant | PSEN1 | GRCh38.p7 | 14:73146060 | TCCAGTGAGCGAGAT[C/T]GTGCCACTACATTGC | 5663 |
rs60369636 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | PSEN1 | GRCh38.p7 | 14:73142974 | TACTCCCACCTACTC[C/T]TCAATTCGGGTCCCA | 5663 |
rs60619903 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | PSEN1 | GRCh38.p7 | 14:73147250 | TGGCCTCCCAAAGTG[C/G]TGGGATTACAGGCAT | 5663 |
rs60898691 | in-del | -/AA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73150787 | AAAAAAAAAAAAAAA[-/AA]GCCAGGTGCGGTGGC | 5663 |
rs60922931 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167846 | TTTTTTTTTTTTTTT[-/T]GCTTCGAAGAATGAT | 5663 |
rs60926424 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PSEN1 | GRCh38.p7 | 14:73176666 | GTAAAGGTTTTCCCA[A/G]TCTTGGGCAGTGACA | 5663 |
rs61141098 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | PSEN1 | GRCh38.p7 | 14:73174283 | ACCCAGGCTGGAGTG[A/G]AGTGCAGTGGCACGA | 5663 |
rs61986861 | snp | C/G | 0.0517044 | 0.152246 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139080 | CCAGATCAGGAGATG[C/G]AGACCATCCTGGCTC | 5663 |
rs61986862 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139082 | AGATCAGGAGATGGA[A/G]ACCATCCTGGCTCAC | 5663 |
rs61986863 | snp | A/T | 0.0517044 | 0.152246 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139123 | CCCGTCTCTACTAAA[A/T]GTACAAAAAATTAGC | 5663 |
rs61986865 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141851 | GGCTGGCAGATCACG[A/G]GGTCAGGAGATCGAG | 5663 |
rs61986866 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145048 | CAGGCACGAGCTACC[A/G]TGCCCAGCTAATTTT | 5663 |
rs61986877 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151860 | AGGTGTGAGCTACTG[C/T]GCCCAACCTAAAATA | 5663 |
rs61986878 | snp | A/G | 0.320575 | 0.239832 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152598 | GTGTGACAGAGTGAG[A/G]CTGTCTCAAAAAAAG | 5663 |
rs61986879 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | PSEN1 | GRCh38.p7 | 14:73153945 | TCTCGAACTCCTGAC[C/T]TCAAGTGATCTGACC | 5663 |
rs61986880 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154195 | AACACAACTATGTAT[A/G]CCTGTGTGTATATAT | 5663 |
rs61986881 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158345 | ATCTATTTTTAAGAC[A/G]GAGTTTTGCTCCATC | 5663 |
rs61986882 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | PSEN1 | GRCh38.p7 | 14:73159589 | TTTTTAAAAAAGACT[A/G]TTTTCTCCACTGAAG | 5663 |
rs61986883 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160900 | GCAAGCTCCACCTGC[C/T]GGGTTCATGCTATTG | 5663 |
rs61986884 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | PSEN1 | GRCh38.p7 | 14:73161798 | ACACAAGGCCCTCAC[C/T]GTAGATCACATTATT | 5663 |
rs61986885 | snp | A/C | 0.143284 | 0.226079 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168337 | TCCAGCCTGGGCAAC[A/C]GAGTGAGACTCTGTC | 5663 |
rs61986886 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PSEN1 | GRCh38.p7 | 14:73175144 | TTTGTTTTTTTCCCC[A/G]AGACGAAGTCTCGCT | 5663 |
rs61986887 | snp | A/C | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73175477 | TAAGACCTATCTCTA[A/C]CAAAAAAAAAAAAAA | 5663 |
rs61986888 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181907 | ACCTCCATGGTAGCT[A/G]GGACTACAGGCACCT | 5663 |
rs61986889 | snp | A/G | 0.132409 | 0.220618 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181919 | GCTGGGACTACAGGC[A/G]CCTGCCACCACGCCT | 5663 |
rs61986891 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73185429 | GCCAACACAGCGAAA[C/T]CCCGTCTCCACCAAA | 5663 |
rs61986892 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187769 | ACTAAGTGTTCCGAA[C/T]ATATAAAAAGAAAAA | 5663 |
rs61986893 | snp | A/T | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73190483 | CAGACCTTGTCTCTA[A/T]TTAAAAAAAAAAAAA | 5663 |
rs61986894 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194637 | GCAGTGGCGTGATCT[C/T]GGCTCACTGCAAGCT | 5663 |
rs61986895 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194673 | TCCCAGGTTCATGCC[A/G]TTCTCCTGCCTCAGC | 5663 |
rs61986896 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194819 | ATGATTCACCTGCCT[C/T]GGCCTCCCAAAGTGT | 5663 |
rs61986897 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201249 | CACGCCGCCACGCCC[A/G]GCTAATTTTTGTATT | 5663 |
rs61986898 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204471 | TACTGCTTGAAGCCA[A/G]ATATGGCCCATGGCT | 5663 |
rs61986899 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205272 | ACGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 5663 |
rs61986900 | snp | A/T | 0.0517044 | 0.152246 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205407 | TGGCGTGAACCCAGG[A/T]GACGGAGCTTGCAGT | 5663 |
rs61986901 | snp | G/T | 0.107341 | 0.205301 | intron-variant | PSEN1 | GRCh38.p7 | 14:73207652 | GGATCCTTAGGGTGT[G/T]ACTTTGCTAGCCAGA | 5663 |
rs61986902 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | PSEN1 | GRCh38.p7 | 14:73207669 | CTTTGCTAGCCAGAA[A/G]CCTCTGTGGCTGGTG | 5663 |
rs61986903 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | PSEN1 | GRCh38.p7 | 14:73209008 | AGGGGGCTGGCATGT[C/T]AGTGCTGCCCCAAGC | 5663 |
rs61986904 | snp | C/T | 0.112631 | 0.208878 | intron-variant | PSEN1 | GRCh38.p7 | 14:73215299 | TTAAGAAGTGGAAAA[C/T]AAGGCCAGGTGTGGT | 5663 |
rs61986928 | snp | G/T | 0.118991 | 0.214262 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216688 | CGCTTGAACCTGGGC[G/T]GCAGAGTCTGCAGTG | 5663 |
rs63749805 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73173577 | GTAGAATCTATACCC[C/T]ATTCACAGAAGATAC | 5663 |
rs63749806 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73186902 | TGTTGCTGTTCTTTT[C/T]TTCATTCATTTACTT | 5663 |
rs63749824 | snp | C/T | 1.64814e-05 | 0.00287061 | PSEN1 | 14 | allele_origin=T(germline)/C(germline) | 14:73170945 | CATTGAAATATGGCG[C/T]CAAGCATGTGATCAT | 5663 |
rs63749835 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73192799 | GTGCCCTCATGGCCC[C/T]GGTGTTTATCAAGTA | 5663 |
rs63749836 | snp | A/G | | | missense | PSEN1 | GRCh38.p7 | 14:73192786 | CTCATTATGATTAGT[A/G]CCCTCATGGCCCTGG | 5663 |
rs63749860 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73217153 | TTGGATTGGGAGATT[C/T]CATTTTCTACAGTGT | 5663 |
rs63749880 | snp | A/G | | | missense | PSEN1 | GRCh38.p7 | 14:73192720 | AATTTTGGTGTGGTG[A/G]GAATGATTTCCATTC | 5663 |
rs63749885 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73186859 | CTTTTCTAGGTCATC[C/T]ATGCCTGGCTTATTA | 5663 |
rs63749891 | snp | C/G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73198094 | AAACAGCTCAGGAGA[C/G/T]AAATGAAACGCTTTT | 5663 |
rs63749911 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73186901 | TTGTTGCTGTTCTTT[C/T]TTTCATTCATTTACT | 5663 |
rs63749925 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73219191 | GCATTGCCAGCTCTT[C/T]CAATCTCCATCACCT | 5663 |
rs63749937 | snp | C/G | | | missense | PSEN1 | GRCh38.p7 | 14:73198105 | GAGAGAAATGAAACG[C/G]TTTTTCCAGCTCTCA | 5663 |
rs63749961 | snp | G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73192772 | TCCAGCAGGCATATC[G/T]CATTATGATTAGTGC | 5663 |
rs63749962 | snp | G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73173570 | TTTTATTGTAGAATC[G/T]ATACCCCATTCACAG | 5663 |
rs63749967 | snp | C/G | | | missense | PSEN1 | GRCh38.p7 | 14:73170953 | TATGGCGCCAAGCAT[C/G]TGATCATGCTCTTTG | 5663 |
rs63749970 | snp | A/T | | | missense | PSEN1 | GRCh38.p7 | 14:73192780 | GCATATCTCATTATG[A/T]TTAGTGCCCTCATGG | 5663 |
rs63749987 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73192750 | CACTGGAAAGGTCCA[C/T]TTCGACTCCAGCAGG | 5663 |
rs63750001 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73219188 | AAAGCATTGCCAGCT[C/T]TTCCAATCTCCATCA | 5663 |
rs63750004 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73173655 | TCATGATCAGTGTCA[C/T]TGTTGTCATGACTAT | 5663 |
rs63750009 | snp | A/G | | | missense | PSEN1 | GRCh38.p7 | 14:73192760 | GTCCACTTCGACTCC[A/G]GCAGGCATATCTCAT | 5663 |
rs63750050 | snp | G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73198106 | AGAGAAATGAAACGC[G/T]TTTTCCAGCTCTCAT | 5663 |
rs63750053 | snp | G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73192721 | ATTTTGGTGTGGTGG[G/T]AATGATTTCCATTCA | 5663 |
rs63750082 | snp | C/G/T | 1.6473e-05 | 0.00286988 | PSEN1 | 14 | allele_origin=G(germline)/T(germline)/C(germline) | 14:73192712 | TGATCTGGAATTTTG[C/G/T]TGTGGTGGGAATGAT | 5663 |
rs63750083 | snp | A/C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73219177 | CCATTTTCAAGAAAG[A/C/T]ATTGCCAGCTCTTCC | 5663 |
rs63750155 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73186904 | TTGCTGTTCTTTTTT[C/T]CATTCATTTACTTGG | 5663 |
rs63750218 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73217171 | TTTTCTACAGTGTTC[C/T]GGTTGGTAAAGCCTC | 5663 |
rs63750219 | snp | G/T | | | splice-acceptor-variant | PSEN1 | GRCh38.p7 | 14:73206385 | TTGTCTTTCCCAACA[G/T]CAACAATGGTGTGGT | 5663 |
rs63750227 | snp | A/G | | | missense | PSEN1 | GRCh38.p7 | 14:73217221 | TGGAACACAACCATA[A/G]CCTGTTTCGTAGCCA | 5663 |
rs63750231 | snp | A/C/G | | | missense | PSEN1 | GRCh38.p7 | 14:73198100 | CTCAGGAGAGAAATG[A/C/G]AACGCTTTTTCCAGC | 5663 |
rs63750248 | snp | A/C/G/T | 8.92553e-05 | 0.00667987 | PSEN1 | 14 | allele_origin=G(germline)/C(unknown) | 14:73198047 | TTTAGTGGCTGTTTT[A/C/G/T]TGTCCGAAAGGTCCA | 5663 |
rs63750249 | snp | A/G | | | missense | PSEN1 | GRCh38.p7 | 14:73219200 | GCTCTTCCAATCTCC[A/G]TCACCTTTGGGCTTG | 5663 |
rs63750265 | snp | C/G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73186869 | TCATCCATGCCTGGC[C/G/T]TATTATATCATCTCT | 5663 |
rs63750284 | snp | C/G | | | missense | PSEN1 | GRCh38.p7 | 14:73198082 | GTATGCTGGTTGAAA[C/G]AGCTCAGGAGAGAAA | 5663 |
rs63750298 | snp | A/C | | | missense | PSEN1 | GRCh38.p7 | 14:73206388 | TCTTTCCCAACAGCA[A/C]CAATGGTGTGGTTGG | 5663 |
rs63750299 | snp | G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73186890 | TATCATCTCTATTGT[G/T]GCTGTTCTTTTTTTC | 5663 |
rs63750301 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73198052 | TGGCTGTTTTGTGTC[C/T]GAAAGGTCCACTTCG | 5663 |
rs63750306 | snp | A/C/G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73173663 | AGTGTCATTGTTGTC[A/C/G/T]TGACTATCCTCCTGG | 5663 |
rs63750307 | in-del | -/ATCATG | | | cds-indel | PSEN1 | GRCh38.p7 | 14:73170956 | GGCGCCAAGCATGTG[-/ATCATG]CTCTTTGTCCCTGTG | 5663 |
rs63750311 | snp | A/C | | | missense | PSEN1 | GRCh38.p7 | 14:73192647 | ATTTTTTTTCAGGGA[A/C]GTGTTTAAAACCTAT | 5663 |
rs63750321 | snp | G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73171024 | TAAGTCAGTCAGCTT[G/T]TATACCCGGAAGGAT | 5663 |
rs63750322 | snp | A/T | | | missense | PSEN1 | GRCh38.p7 | 14:73173654 | ATCATGATCAGTGTC[A/T]TTGTTGTCATGACTA | 5663 |
rs63750323 | snp | C/G/T | 1.64779e-05 | 0.00287031 | PSEN1 | 14 | allele_origin=G(germline)/T(unknown) | 14:73217129 | TTTCCTTTTTAGGGG[C/G/T]AGTAAAACTTGGATT | 5663 |
rs63750324 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73198111 | AATGAAACGCTTTTT[C/T]CAGCTCTCATTTACT | 5663 |
rs63750325 | snp | A/T | | | missense | PSEN1 | GRCh38.p7 | 14:73171022 | ATTAAGTCAGTCAGC[A/T]TTTATACCCGGAAGG | 5663 |
rs63750353 | snp | A/G | | | missense | PSEN1 | GRCh38.p7 | 14:73173630 | CTGCACTCAATTCTG[A/G]ATGCTGCCATCATGA | 5663 |
rs63750378 | snp | A/G | | | missense | PSEN1 | GRCh38.p7 | 14:73173594 | TTCACAGAAGATACC[A/G]AGACTGTGGGCCAGA | 5663 |
rs63750391 | snp | A/G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73173665 | TGTCATTGTTGTCAT[A/G/T]ACTATCCTCCTGGTG | 5663 |
rs63750418 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73186877 | GCCTGGCTTATTATA[C/T]CATCTCTATTGTTGC | 5663 |
rs63750444 | snp | A/G | | | missense | PSEN1 | GRCh38.p7 | 14:73192745 | CCATTCACTGGAAAG[A/G]TCCACTTCGACTCCA | 5663 |
rs63750450 | snp | A/G | | | missense | PSEN1 | GRCh38.p7 | 14:73173571 | TTTATTGTAGAATCT[A/G]TACCCCATTCACAGA | 5663 |
rs63750470 | in-del | -/ACC | | | cds-indel | PSEN1 | GRCh38.p7 | 14:73219203 | CTTCCAATCTCCATC[-/ACC]TTTGGGCTTGTTTTC | 5663 |
rs63750487 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73192771 | CTCCAGCAGGCATAT[C/T]TCATTATGATTAGTG | 5663 |
rs63750522 | snp | A/G | | | missense | PSEN1 | GRCh38.p7 | 14:73173644 | GAATGCTGCCATCAT[A/G]ATCAGTGTCATTGTT | 5663 |
rs63750524 | snp | A/C | | | missense | PSEN1 | GRCh38.p7 | 14:73198095 | AACAGCTCAGGAGAG[A/C]AATGAAACGCTTTTT | 5663 |
rs63750526 | snp | A/C | | | missense | PSEN1 | GRCh38.p7 | 14:73192832 | TCCCTGAATGGACTG[A/C]GTGGCTCATCTTGGC | 5663 |
rs63750543 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73198048 | TTAGTGGCTGTTTTG[C/T]GTCCGAAAGGTCCAC | 5663 |
rs63750550 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73173576 | TGTAGAATCTATACC[C/T]CATTCACAGAAGATA | 5663 |
rs63750569 | snp | A/G | | | missense | PSEN1 | GRCh38.p7 | 14:73192711 | CTGATCTGGAATTTT[A/G]GTGTGGTGGGAATGA | 5663 |
rs63750577 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73186881 | GGCTTATTATATCAT[C/T]TCTATTGTTGCTGTT | 5663 |
rs63750588 | snp | A/T | | | missense | PSEN1 | GRCh38.p7 | 14:73173687 | CTCCTGGTGGTTCTG[A/T]ATAAATACAGGTGCT | 5663 |
rs63750590 | snp | A/G | | | missense | PSEN1 | GRCh38.p7 | 14:73186860 | TTTTCTAGGTCATCC[A/G]TGCCTGGCTTATTAT | 5663 |
rs63750592 | snp | A/G | 0.000347501 | 0.0131769 | PSEN1 | 14 | allele_origin=G(germline)/A(unknown) | 14:73170813 | ATGACAATAGAGAAC[A/G]GCAGGAGCACAACGA | 5663 |
rs63750599 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73170963 | AGCATGTGATCATGC[C/T]CTTTGTCCCTGTGAC | 5663 |
rs63750601 | snp | G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73170995 | CTCTGCATGGTGGTG[G/T]TCGTGGCTACCATTA | 5663 |
rs63750631 | in-del | -/TTATAT | | | cds-indel | PSEN1 | GRCh38.p7 | 14:73173693 | TGGTTCTGTATAAAT[-/TTATAT]ACAGGTGCTATAAGG | 5663 |
rs63750634 | snp | G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73192843 | ACTGCGTGGCTCATC[G/T]TGGCTGTGATTTCAG | 5663 |
rs63750646 | snp | C/G | | | missense | PSEN1 | GRCh38.p7 | 14:73217147 | TAAAACTTGGATTGG[C/G]AGATTTCATTTTCTA | 5663 |
rs63750680 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73198076 | CACTTCGTATGCTGG[C/T]TGAAACAGCTCAGGA | 5663 |
rs63750687 | snp | C/G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73217137 | TTAGGGGGAGTAAAA[C/G/T]TTGGATTGGGAGATT | 5663 |
rs63750730 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73173574 | ATTGTAGAATCTATA[C/T]CCCATTCACAGAAGA | 5663 |
rs63750761 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73192751 | ACTGGAAAGGTCCAC[C/T]TCGACTCCAGCAGGC | 5663 |
rs63750762 | in-del | -/TCG | | | cds-indel | PSEN1 | GRCh38.p7 | 14:73211868 | TCTAGGGCCTCATCG[-/TCG]CTCTACACCTGAGTC | 5663 |
rs63750771 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73186896 | CTCTATTGTTGCTGT[C/T]CTTTTTTTCATTCAT | 5663 |
rs63750772 | snp | A/C | | | missense | PSEN1 | GRCh38.p7 | 14:73198079 | TTCGTATGCTGGTTG[A/C]AACAGCTCAGGAGAG | 5663 |
rs63750779 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73198061 | TGTGTCCGAAAGGTC[C/T]ACTTCGTATGCTGGT | 5663 |
rs63750799 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73192787 | TCATTATGATTAGTG[C/T]CCTCATGGCCCTGGT | 5663 |
rs63750800 | snp | A/G | | | missense | PSEN1 | GRCh38.p7 | 14:73173585 | TATACCCCATTCACA[A/G]AAGATACCGAGACTG | 5663 |
rs63750802 | snp | G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73219144 | CACAGGGTTTGTGCC[G/T]TACATTATTACTCCT | 5663 |
rs63750815 | snp | G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73170974 | ATGCTCTTTGTCCCT[G/T]TGACTCTCTGCATGG | 5663 |
rs63750831 | snp | A/G | 1.64792e-05 | 0.00287042 | PSEN1 | 14 | allele_origin=G(germline)/A(unknown) | 14:73170989 | GTGACTCTCTGCATG[A/G]TGGTGGTCGTGGCTA | 5663 |
rs63750852 | snp | A/G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73170998 | TGCATGGTGGTGGTC[A/G/T]TGGCTACCATTAAGT | 5663 |
rs63750858 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73192804 | CTCATGGCCCTGGTG[C/T]TTATCAAGTACCTCC | 5663 |
rs63750861 | snp | A/C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73192732 | GTGGGAATGATTTCC[A/C/T]TTCACTGGAAAGGTC | 5663 |
rs63750863 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73198112 | ATGAAACGCTTTTTC[C/T]AGCTCTCATTTACTC | 5663 |
rs63750879 | in-del | -/TAT | | | cds-indel | PSEN1 | GRCh38.p7 | 14:73186870 | CATCCATGCCTGGCT[-/TAT]TATATCATCTCTATT | 5663 |
rs63750883 | snp | G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73217165 | ATTTCATTTTCTACA[G/T]TGTTCTGGTTGGTAA | 5663 |
rs63750886 | snp | C/G | | | missense | PSEN1 | GRCh38.p7 | 14:73198072 | GGTCCACTTCGTATG[C/G]TGGTTGAAACAGCTC | 5663 |
rs63750888 | snp | A/C | | | missense | PSEN1 | GRCh38.p7 | 14:73192828 | TACCTCCCTGAATGG[A/C]CTGCGTGGCTCATCT | 5663 |
rs63750900 | snp | A/G | 1.74027e-05 | 0.00294975 | PSEN1 | 14 | allele_origin=G(germline)/A(unknown) | 14:73198067 | CGAAAGGTCCACTTC[A/G]TATGCTGGTTGAAAC | 5663 |
rs63750907 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73173667 | TCATTGTTGTCATGA[C/T]TATCCTCCTGGTGGT | 5663 |
rs63750929 | snp | G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73217177 | ACAGTGTTCTGGTTG[G/T]TAAAGCCTCAGCAAC | 5663 |
rs63750941 | snp | A/C | | | missense | PSEN1 | GRCh38.p7 | 14:73211907 | CTGTCCAGGAACTTT[A/C]CAGCAGTATCCTCGC | 5663 |
rs63750963 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73186884 | TTATTATATCATCTC[C/T]ATTGTTGCTGTTCTT | 5663 |
rs63750964 | snp | G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73198042 | CTAGATTTAGTGGCT[G/T]TTTTGTGTCCGAAAG | 5663 |
rs63751003 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73192735 | GGAATGATTTCCATT[C/T]ACTGGAAAGGTCCAC | 5663 |
rs63751010 | snp | G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73186865 | TAGGTCATCCATGCC[G/T]GGCTTATTATATCAT | 5663 |
rs63751019 | snp | C/G | | | missense | PSEN1 | GRCh38.p7 | 14:73198066 | CCGAAAGGTCCACTT[C/G]GTATGCTGGTTGAAA | 5663 |
rs63751024 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73192793 | TGATTAGTGCCCTCA[C/T]GGCCCTGGTGTTTAT | 5663 |
rs63751025 | snp | G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73186893 | CATCTCTATTGTTGC[G/T]GTTCTTTTTTTCATT | 5663 |
rs63751032 | snp | G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73219156 | GCCTTACATTATTAC[G/T]CCTTGCCATTTTCAA | 5663 |
rs63751037 | snp | A/G | | | missense | PSEN1 | GRCh38.p7 | 14:73173642 | CTGAATGCTGCCATC[A/G]TGATCAGTGTCATTG | 5663 |
rs63751051 | snp | G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73217126 | ACCTTTCCTTTTTAG[G/T]GGGAGTAAAACTTGG | 5663 |
rs63751066 | snp | G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73217167 | TTCATTTTCTACAGT[G/T]TTCTGGTTGGTAAAG | 5663 |
rs63751068 | snp | G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73186920 | CATTCATTTACTTGG[G/T]GTAAGTTGTGAAATT | 5663 |
rs63751071 | snp | G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73173656 | CATGATCAGTGTCAT[G/T]GTTGTCATGACTATC | 5663 |
rs63751072 | snp | C/G | | | missense | PSEN1 | GRCh38.p7 | 14:73192761 | TCCACTTCGACTCCA[C/G]CAGGCATATCTCATT | 5663 |
rs63751102 | snp | G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73198049 | TAGTGGCTGTTTTGT[G/T]TCCGAAAGGTCCACT | 5663 |
rs63751106 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73173643 | TGAATGCTGCCATCA[C/T]GATCAGTGTCATTGT | 5663 |
rs63751130 | snp | C/G | | | missense | PSEN1 | GRCh38.p7 | 14:73192798 | AGTGCCCTCATGGCC[C/G]TGGTGTTTATCAAGT | 5663 |
rs63751139 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73198115 | AAACGCTTTTTCCAG[C/T]TCTCATTTACTCCTG | 5663 |
rs63751141 | snp | C/G | | | missense | PSEN1 | GRCh38.p7 | 14:73170984 | TCCCTGTGACTCTCT[C/G]CATGGTGGTGGTCGT | 5663 |
rs63751144 | snp | A/C | | | missense | PSEN1 | GRCh38.p7 | 14:73186892 | TCATCTCTATTGTTG[A/C]TGTTCTTTTTTTCAT | 5663 |
rs63751163 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73192844 | CTGCGTGGCTCATCT[C/T]GGCTGTGATTTCAGT | 5663 |
rs63751164 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73211874 | GGCCTCATCGCTCTA[C/T]ACCTGAGTCACGAGC | 5663 |
rs63751174 | snp | A/G | 4.94279e-05 | 0.00497107 | PSEN1 | 14 | allele_origin=G(germline)/A(unknown) | 14:73211886 | CTACACCTGAGTCAC[A/G]AGCTGCTGTCCAGGA | 5663 |
rs63751210 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73186878 | CCTGGCTTATTATAT[C/T]ATCTCTATTGTTGCT | 5663 |
rs63751223 | snp | C/G | | | missense | PSEN1 | GRCh38.p7 | 14:73219161 | ACATTATTACTCCTT[C/G]CCATTTTCAAGAAAG | 5663 |
rs63751229 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73198060 | TTGTGTCCGAAAGGT[C/T]CACTTCGTATGCTGG | 5663 |
rs63751235 | snp | C/G | | | missense | PSEN1 | GRCh38.p7 | 14:73198117 | ACGCTTTTTCCAGCT[C/G]TCATTTACTCCTGTA | 5663 |
rs63751254 | snp | A/G | | | missense | PSEN1 | GRCh38.p7 | 14:73217210 | CCAGTGGAGACTGGA[A/G]CACAACCATAGCCTG | 5663 |
rs63751272 | snp | A/T | | | missense | PSEN1 | GRCh38.p7 | 14:73173587 | TACCCCATTCACAGA[A/T]GATACCGAGACTGTG | 5663 |
rs63751278 | snp | A/G | | | missense | PSEN1 | GRCh38.p7 | 14:73173631 | TGCACTCAATTCTGA[A/G]TGCTGCCATCATGAT | 5663 |
rs63751287 | snp | A/G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73192792 | ATGATTAGTGCCCTC[A/G/T]TGGCCCTGGTGTTTA | 5663 |
rs63751292 | snp | A/G | | | missense | PSEN1 | GRCh38.p7 | 14:73173688 | TCCTGGTGGTTCTGT[A/G]TAAATACAGGTGCTA | 5663 |
rs63751309 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73192733 | TGGGAATGATTTCCA[C/T]TCACTGGAAAGGTCC | 5663 |
rs63751316 | snp | G/T | | | missense | PSEN1 | GRCh38.p7 | 14:73219139 | TTCTCCACAGGGTTT[G/T]TGCCTTACATTATTA | 5663 |
rs63751320 | snp | A/C | | | missense | PSEN1 | GRCh38.p7 | 14:73192862 | CTGTGATTTCAGTAT[A/C]TGGTAAAACCCAAGA | 5663 |
rs63751399 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73171047 | GGAAGGATGGGCAGC[C/T]GTACGTATGAGTTTT | 5663 |
rs63751416 | snp | C/G | | | missense | PSEN1 | GRCh38.p7 | 14:73217170 | ATTTTCTACAGTGTT[C/G]TGGTTGGTAAAGCCT | 5663 |
rs63751420 | snp | C/T | | | missense | PSEN1 | GRCh38.p7 | 14:73198040 | TTCTAGATTTAGTGG[C/T]TGTTTTGTGTCCGAA | 5663 |
rs63751441 | snp | C/G/T | 6.59044e-05 | 0.00574002 | PSEN1 | 14 | allele_origin=G(unknown)/C(germline) | 14:73173684 | ATCCTCCTGGTGGTT[C/G/T]TGTATAAATACAGGT | 5663 |
rs63751458 | in-del | -/CTT | | | cds-indel | PSEN1 | GRCh38.p7 | 14:73186868 | GTCATCCATGCCTGG[-/CTT]ATTATATCATCTCTA | 5663 |
rs63751475 | in-del | -/G | | | splice-donor-variant | PSEN1 | GRCh38.p7 | 14:73171048 | GAAGGATGGGCAGCT[-/G]TACGTATGAGTTTTG | 5663 |
rs63751479 | snp | C/G | | | missense | PSEN1 | GRCh38.p7 | 14:73192794 | GATTAGTGCCCTCAT[C/G]GCCCTGGTGTTTATC | 5663 |
rs63751484 | snp | C/G | | | missense | PSEN1 | GRCh38.p7 | 14:73186867 | GGTCATCCATGCCTG[C/G]CTTATTATATCATCT | 5663 |
rs66748161 | in-del | -/A | 0.211516 | 0.24702 | intron-variant | PSEN1 | GRCh38.p7 | 14:73188201 | CAAAGTGCTGGAATT[-/A]ACAGGCCTGAGCCAC | 5663 |
rs67647403 | snp | C/T | 0.32768 | 0.237625 | intron-variant | PSEN1 | GRCh38.p7 | 14:73155770 | GCGATTCTCCCGTCT[C/T]GGCCTCCTGAAGCAT | 5663 |
rs67735228 | in-del | -/A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73147060 | AAAAAAAAAAAAAAA[-/A/C]AGAATGGCTGACTCC | 5663 |
rs68084031 | snp | A/G | 0.328382 | 0.237395 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154868 | CACTTCTTACCTATC[A/G]GTGAGTTAAAATTGA | 5663 |
rs71112708 | in-del | -/ATAG | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158332 | AACTCCGTCTTAAAA[-/ATAG]ATAGATAGATAGATA | 5663 |
rs71427179 | snp | A/G | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73161159 | TTTGTATTTTTTGTA[A/G]AGACGGAGTTTCACC | 5663 |
rs71427180 | snp | C/T | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73161747 | TGGCTGACCTCAGTT[C/T]TCTGGCCCCTTCAGA | 5663 |
rs71427181 | snp | A/C | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196811 | AAATGCATTTAAGTG[A/C]CAATAATGTGAATAC | 5663 |
rs71450213 | in-del | -/C | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158489 | TGCCACCACACCCAG[-/C]TAATTTTTGTATTTG | 5663 |
rs72098080 | in-del | -/CT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73162448 | CTCGCGCGCTCTCTC[-/CT]TCTCTCTCTCCATGA | 5663 |
rs72734454 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143433 | GTTTACACTCTCTCT[C/G]TAACTCTGTGCAGGC | 5663 |
rs72734455 | snp | C/T | 0.327211 | 0.237778 | intron-variant | PSEN1 | GRCh38.p7 | 14:73165247 | AGGCATGAGCCACCA[C/T]GCCCGGCCCAAACTG | 5663 |
rs72734456 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173851 | TTTTCTTCCTCCTCA[C/T]TGTGGAACATTCAAA | 5663 |
rs72734460 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PSEN1 | GRCh38.p7 | 14:73199208 | AATACTAGAGCTTGG[A/G]AAAAAGTTGATATTT | 5663 |
rs73305007 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136745 | ACCCCGTGTGGGAAA[C/T]CAGGAGGGGCGGCCC | 5663 |
rs73305016 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143063 | TGTTCATGGCTAAGA[A/C]TGTTAAAAAGTCTCC | 5663 |
rs73305034 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PSEN1 | GRCh38.p7 | 14:73167619 | AACTATAGCACCCTC[C/T]TTTATCCCTTACCCT | 5663 |
rs73305038 | snp | A/T | 0.0807149 | 0.183963 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168916 | GCCTGCGCCTGCCAG[A/T]GAGGAGCAACTGGCT | 5663 |
rs73305043 | snp | C/G | 0.0810805 | 0.184299 | intron-variant | PSEN1 | GRCh38.p7 | 14:73172512 | AGGTGTAATAACAAA[C/G]TTATTCACAAATTTG | 5663 |
rs73305051 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PSEN1 | GRCh38.p7 | 14:73178699 | CTAAAATTCCTATAT[A/G]GCCCGTCTTTACATT | 5663 |
rs73305053 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192446 | ACCCTGGCTCAAAAA[C/G]AAAAACAAAAACAAA | 5663 |
rs73305061 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193859 | AGAACGTCTTGCTAT[A/G]TTGCCTAGGCTGGTC | 5663 |
rs73305064 | snp | G/T | 0.162581 | 0.234218 | intron-variant | PSEN1 | GRCh38.p7 | 14:73207128 | TCCGGATTACCCTGG[G/T]CAACTTATACCTTAC | 5663 |
rs74061003 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208191 | TCTTCTCTCCTTCTC[A/G]CCACCTGCAACGTGG | 5663 |
rs74061004 | snp | C/T | 0.039522 | 0.134904 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211001 | ACTCCCCGCTCCTTT[C/T]CCAATCCACCCTCCA | 5663 |
rs74061005 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212055 | TAATTCTATATCACA[C/T]GTAACTTTTATTTGG | 5663 |
rs74061006 | snp | A/G | 0.0154538 | 0.0865337 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222647 | GCAAAGATGAATAAG[A/G]TAAATTCTCAGAATG | 5663 |
rs74061007 | snp | A/G | 0.0154538 | 0.0865337 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222855 | TTTGCTGTTATGTCT[A/G]TAAGGAACAGTTTGA | 5663 |
rs74062647 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162498 | AGAGAGAGAGAGCAC[A/G]CGAACAAGCGATTGA | 5663 |
rs74062651 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204847 | TTTGAGTCTGGCCTG[A/G]GCAACGTAGTGAGAC | 5663 |
rs74062653 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205802 | GTAGAGATGCACATG[A/T]GTATATCTAGATCTA | 5663 |
rs74424999 | snp | G/T | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169680 | TTTTTTTTTTTTTTT[G/T]AGCCTTGCTTTGTCA | 5663 |
rs74458740 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73156488 | AAATATTTATGAAGG[A/T]AATGATATATCTAAG | 5663 |
rs74653211 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157587 | AAATGTCCATTACCT[C/T]CAGAAGTTTCTTCAT | 5663 |
rs74676595 | snp | A/C | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73140995 | GGGCAGTGGCTATCC[A/C]TGATAAGCTTTTCTC | 5663 |
rs74714816 | snp | A/C | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157568 | ACCACAGTTAAAATA[A/C]TGAAAATGTCCATTA | 5663 |
rs74727279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141658 | GGCATGGTGGTGGGC[A/G]TCTGTAATCCTAGCT | 5663 |
rs74820432 | snp | A/C | 0.0633504 | 0.166319 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156559 | GGAGTAGATGAAACA[A/C]GATTAGCATGAGTTC | 5663 |
rs74828099 | snp | A/C | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216758 | AGCAAAACTCCATCT[A/C]AAAAAAAAAAAAAAT | 5663 |
rs74856884 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158961 | ACATTTCTCTATTGA[A/G]TAATGATGTTGAGTT | 5663 |
rs74981834 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | PSEN1 | GRCh38.p7 | 14:73146334 | TTGGGACTACAGATG[C/T]ATCCCACCTGCACCC | 5663 |
rs75051290 | snp | C/T | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157306 | AATTTTTTTGTATAC[C/T]TTTTTTTTTTTAAGT | 5663 |
rs75057334 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154865 | CTTCACTTCTTACCT[A/G]TCAGTGAGTTAAAAT | 5663 |
rs75151660 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73193891 | TGAACTCTTGGGCTC[A/C]AGCAATCCTCCTACC | 5663 |
rs75179141 | snp | A/T | 0.0244538 | 0.107838 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134536 | TTTATTTATTTATTT[A/T]TATTTTTTGAGACAT | 5663 |
rs75181239 | snp | G/T | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200719 | CTTGTAGATTTTTTT[G/T]GCCAATTTTTCTGTT | 5663 |
rs75227261 | in-del | -/TTTT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73147057 | TTCTTTTTTTTTTTT[-/TTTT]CTGCAACCTCCACCT | 5663 |
rs75233854 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | PSEN1 | GRCh38.p7 | 14:73153854 | AGTAGTTGGGATTAA[C/T]AGGGTTGTGCCACCA | 5663 |
rs75234948 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210007 | CCTCCATCCTAGTTA[C/T]TTCCAAACACTCCCC | 5663 |
rs75266743 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151330 | TTCATTAGTCTGTGT[A/G]CACTTGTGTGAGTTT | 5663 |
rs75331149 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73156490 | ATATTTATGAAGGAA[A/C]TGATATATCTAAGAT | 5663 |
rs75363802 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160701 | CTTTTCATGTGCTTG[C/T]TGGCTATTTGTATAT | 5663 |
rs75389647 | snp | C/T | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160986 | TTTTTTTTTTTTTTT[C/T]TTCGATACAAGGTTT | 5663 |
rs75467834 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PSEN1 | GRCh38.p7 | 14:73176780 | TTATGGATGAGGCAC[C/T]GAGGCAGGGGTCACA | 5663 |
rs75527985 | snp | A/C | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73175479 | AGACCTATCTCTACC[A/C]AAAAAAAAAAAAATT | 5663 |
rs75563122 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168697 | ATCGTGCAATACAAT[C/T]TTCTGCATATACTAC | 5663 |
rs75650982 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73193894 | ACTCTTGGGCTCAAG[C/T]AATCCTCCTACCTTG | 5663 |
rs75659473 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | PSEN1 | GRCh38.p7 | 14:73202804 | TTAAAACTCAACGTC[C/T]GTGCTCGCTTTAGCA | 5663 |
rs75783609 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PSEN1 | GRCh38.p7 | 14:73166982 | CTATAACAGAATACC[A/G]CAGACTGGGTGATTT | 5663 |
rs75834438 | snp | A/C | | | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73223698 | ATGAATCCAGCTGTG[A/C]TAGTGTTTTTTACAT | 5663 |
rs75894497 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192366 | AGACCACCTGATCTC[C/T]GGAGGTAAAGACTGC | 5663 |
rs75903964 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208309 | AGGAAGAATGAAGTA[C/T]GTGGACAGCTGGAGG | 5663 |
rs75975162 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | PSEN1 | GRCh38.p7 | 14:73170372 | TTGCTCTGGTCCAAA[C/T]GCCTCTGACACAAGG | 5663 |
rs76018359 | snp | A/C | 0.5 | 0 | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73223938 | GCAAGACTCTGTCTC[A/C]AAAAAAAAAAAGTTT | 5663 |
rs76081140 | in-del | -/AA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73138816 | ATACAAAAAAAAAAA[-/AA]TTAGCCGGGCGTGAT | 5663 |
rs76193270 | snp | A/G | 0.147656 | 0.228091 | intron-variant | PSEN1 | GRCh38.p7 | 14:73215518 | AAATCGGGAGGTGGA[A/G]GTTTCAGTGAGCCGA | 5663 |
rs76339996 | snp | C/T | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73159830 | CTACTTGAGTTTTTT[C/T]CTTTTTTTTGATGAC | 5663 |
rs76356675 | snp | A/G | 0.147656 | 0.228091 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200196 | TTTGAACTTTTTTTC[A/G]TGTGTTTCTTAGTTA | 5663 |
rs76389699 | snp | A/G | 0.130694 | 0.219696 | intron-variant | PSEN1 | GRCh38.p7 | 14:73165780 | AGGTAGTGTGTGGCC[A/G]GGCGCGGTGGCTCAC | 5663 |
rs76426658 | snp | A/G | 0.147321 | 0.227941 | intron-variant | PSEN1 | GRCh38.p7 | 14:73182105 | GTATTAATTTTGGTT[A/G]TCACTGGCCTTTAGA | 5663 |
rs76480544 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73193892 | GAACTCTTGGGCTCA[A/T]GCAATCCTCCTACCT | 5663 |
rs76614784 | snp | C/G | 0.5 | 0 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135157 | GTTAAAGTGGGGGAG[C/G]TGAAGAATTTTAAAA | 5663 |
rs76804037 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | PSEN1 | GRCh38.p7 | 14:73189036 | CCTCAGGTGATCCAC[C/G]TGCCTCCGCCTCCCA | 5663 |
rs76809297 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187618 | CCTAAAGAGAGAATA[C/T]CTAAACAGAGTAAAG | 5663 |
rs76892416 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | PSEN1 | GRCh38.p7 | 14:73175937 | GTATCTGTCGTACCC[C/T]ACCAGTGCTGAATTT | 5663 |
rs76966559 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73172609 | ACTACAGTAGCACAG[C/T]TGAGTGTTTGCACTG | 5663 |
rs77002412 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73159272 | CTGCAGCCTCAAACT[A/C]CTGAGCTCAAAGAAT | 5663 |
rs77029422 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160195 | TATTTTGCTTAGCAT[A/G]ATGTCCTCAAGGTTC | 5663 |
rs77119530 | snp | C/T | 0.21695 | 0.247806 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157126 | CCCTTGAGAAAGATA[C/T]CTTTTTTTTTTTTTG | 5663 |
rs77162241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73142744 | GCACATCTGAGCTTC[A/G]AGATTATTTGTAGTT | 5663 |
rs77244626 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | PSEN1 | GRCh38.p7 | 14:73153313 | CTCTTAGGCACAAAT[A/G]TTAATAATATGTTAA | 5663 |
rs77267908 | snp | C/G | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168093 | GGGTGCGGTGGCTCA[C/G]TCCTATAATCCCAGC | 5663 |
rs77427123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73166834 | TTCCTTTCCATTTCT[C/T]ATAGGGTTTGGATCT | 5663 |
rs77462509 | snp | A/G | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139295 | TTTTTTTTTAAAAAA[A/G]GGCTGGGCACAGTGG | 5663 |
rs77566396 | snp | G/T | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156680 | GTTTGTTTTTTTTTT[G/T]GAGATGGAGTCTTGC | 5663 |
rs77586895 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141419 | AGAAATGATTTGCTC[C/T]TAGTCTCTTAAAAAC | 5663 |
rs77594272 | snp | G/T | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171214 | GGGGTTATTACTTCA[G/T]GTTTTAAGTGGAGAA | 5663 |
rs77609029 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179397 | CAAGGCGGGCAGATT[A/G]CCTGAGCTCATGAGT | 5663 |
rs77628843 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73163231 | CAGGCACACCTACAT[C/G]GTGCTTCATTTTCAG | 5663 |
rs77685348 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73180611 | CAGTTAATTATTATA[C/T]ATAATTTGTTATAAA | 5663 |
rs77778105 | snp | G/T | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157140 | ACCTTTTTTTTTTTT[G/T]GCGAGGGAGTTTCAC | 5663 |
rs77983620 | snp | A/T | 0.040671 | 0.13668 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187132 | AAGTAGAACTGAAAG[A/T]ACTTAAGACTACAGT | 5663 |
rs78132128 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181115 | ATTGTGGGTTTATCC[A/G]TATGAGTAGACTATT | 5663 |
rs78213646 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73163232 | AGGCACACCTACATG[A/G/T]TGCTTCATTTTCAGT | 5663 |
rs78265930 | snp | A/T | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73163942 | GTTTAAAAAAAAAAA[A/T]TCATCCTGGCTGTAG | 5663 |
rs78267161 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | PSEN1 | GRCh38.p7 | 14:73150164 | CCCAGCTTTATTAAA[C/T]CTTAACATCTTATTT | 5663 |
rs78284376 | snp | A/T | 0.0460142 | 0.144533 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194426 | CATGCCTAATTTTTT[A/T]AAAAAAAATTTTTTT | 5663 |
rs78304949 | snp | C/T | 0.163236 | 0.234461 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156466 | TATCTTTTAGAAATA[C/T]ATACTAAAATATTTA | 5663 |
rs78317792 | snp | A/T | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141328 | GGAGAAAAAAAAAAA[A/T]TCACCAAATGGGATG | 5663 |
rs78344413 | in-del | -/TT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73157316 | TATACTTTTTTTTTT[-/TT]AAGTACAGATGGGGT | 5663 |
rs78362186 | snp | G/T | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196949 | TTTTTTTTTTTTTTT[G/T]TGAGACGGAGTCTCG | 5663 |
rs78403601 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145644 | CGAGCCCGGCCTCAT[A/G]CAATTTATTGACTAC | 5663 |
rs78537135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217761 | ATCTTGCTGATAGTG[C/T]TACAGCATGAACCCT | 5663 |
rs78558172 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | PSEN1 | GRCh38.p7 | 14:73189895 | TTGGTCTCCCTTGAC[C/T]GGGTGGGCACTGAGC | 5663 |
rs78560838 | in-del | -/TTGT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73201105 | TGTTTGTTTGTTTGT[-/TTGT]GGCAGAGTCTTGCTG | 5663 |
rs78603551 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157430 | AGGCGTGAGTCACCA[C/T]GCCCAGCCCAAGAAA | 5663 |
rs78682030 | in-del | -/AAAA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73190502 | AAAAAAAAAAAAAAA[-/AAAA]TTAAAATATGCTATC | 5663 |
rs78782780 | snp | A/G | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73172459 | AAACATTGGCAAGCT[A/G]CAGCCACAGGCCAGA | 5663 |
rs78840950 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73151225 | TAGCATTTGTTTTCT[C/G]TTGTGAATATATAAA | 5663 |
rs78841957 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73140897 | TGTATTCTCACTCAG[G/T]GCTCTGCTTCCTTGT | 5663 |
rs78854576 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73193893 | AACTCTTGGGCTCAA[A/G]CAATCCTCCTACCTT | 5663 |
rs78871133 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | PSEN1 | GRCh38.p7 | 14:73215660 | CAACTTAATACGAAG[A/G]CGATAGCCCAAATTT | 5663 |
rs78876005 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73156487 | AAAATATTTATGAAG[C/G]AAATGATATATCTAA | 5663 |
rs78922928 | snp | G/T | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73183127 | TCAGCTTACCTTTTT[G/T]GTTTTTTTGAGATGG | 5663 |
rs78957227 | snp | A/C | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162179 | AGCAAAACTCCATCT[A/C]AAAAAAAAAAAAAAG | 5663 |
rs78959774 | snp | A/C/G | 0.0174175 | 0.0916809 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181724 | AAGGTCTTTACACAC[A/C/G]CCTATACGTGCAGAT | 5663 |
rs79125817 | snp | A/G | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152442 | CCATTTCTACTAAGA[A/G]AAAAAAAAAAAAAAA | 5663 |
rs79252718 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158056 | TTTTGAAATTCGTCC[A/C]TGTTATGTGGTTCCT | 5663 |
rs79282794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73163456 | ATCTTACAGGAGTCA[C/T]TCATTAATTAACTCA | 5663 |
rs79330921 | snp | A/C/G | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73136983 | GGTGTGTCCTTGTCC[A/C/G]GGGGCGACGAGCATT | 5663 |
rs79330923 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73171124 | ATCATCACCTTGAAG[C/G]CCTCTGCATTGAAGG | 5663 |
rs79335076 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139327 | TCACACCTGTAATCT[A/G]CCAGCACTTTGGGAG | 5663 |
rs79362212 | in-del | -/ATTT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73201078 | AGAGAATATCTTTTT[-/ATTT]GTTTGTTTGTTTGTT | 5663 |
rs79480249 | snp | A/T | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73190486 | ACCTTGTCTCTATTT[A/T]AAAAAAAAAAAAAAA | 5663 |
rs79505171 | snp | G/T | 0.173965 | 0.238157 | intron-variant | PSEN1 | GRCh38.p7 | 14:73190634 | CTCACACCTGTAATC[G/T]CAACATTTTTGGAGG | 5663 |
rs79524837 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | PSEN1 | GRCh38.p7 | 14:73191153 | ATTCATTGTTTTTTT[A/T]AAAAAGACATTATAT | 5663 |
rs79620182 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162286 | CAAGATTCCATATTT[C/G]TCCCATCAGATTGGT | 5663 |
rs79668701 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | PSEN1 | GRCh38.p7 | 14:73161731 | GTGTCCGGGTCACAC[A/G]TGGCTGACCTCAGTT | 5663 |
rs79729083 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | PSEN1 | GRCh38.p7 | 14:73213746 | ATGATCTGTAAACAC[A/C]TAAAAAGATACTCAG | 5663 |
rs79769235 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73144705 | GCCTTAGTTTAATAA[C/T]GTCTCTAAGTTTTAC | 5663 |
rs79789313 | snp | G/T | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160987 | TTTTTTTTTTTTTTT[G/T]TCGATACAAGGTTTT | 5663 |
rs79916673 | in-del | -/ACTCA | 0.0517044 | 0.152246 | intron-variant | PSEN1 | GRCh38.p7 | 14:73161482 | TAATTTGCTAGAAAG[-/ACTCA]ACTCAGAGAATGTTT | 5663 |
rs79976215 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162200 | AAAAAAAAAGTTAAA[A/C/T]AGAAAAAGGACATAA | 5663 |
rs80024836 | snp | C/T | 0.17332 | 0.23795 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145134 | CTGGCCTCAAATGAT[C/T]TGTGTGCCTCAGCCT | 5663 |
rs80030711 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73178703 | AATTCCTATATAGCC[C/T]GTCTTTACATTTTTT | 5663 |
rs80043006 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73140780 | TCTAAGTCTTTGTTC[A/G]TTTTTATTGCATTTT | 5663 |
rs80078500 | snp | A/G | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162021 | AAAAAAAAAAATAGA[A/G]AAAGAAACCAAACCA | 5663 |
rs80094658 | snp | C/T | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73147061 | TTTTTTTTTTTTTTT[C/T]TGCAACCTCCACCTC | 5663 |
rs80099383 | in-del | -/ATC | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73188302 | TATTACTAGATCATC[-/ATC]TCTGTATGTGCTAAA | 5663 |
rs80233728 | in-del | -/AAAA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73204540 | ATTTAAAAAAAAAAA[-/AAAA]GAACAAGGAAGAATA | 5663 |
rs80255040 | snp | A/G/T | 0.0244538 | 0.107838 | intron-variant | PSEN1 | GRCh38.p7 | 14:73188378 | AATAGACGGGGTCGG[A/G/T]TGTGGTGGCTCATGT | 5663 |
rs80331025 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173321 | GCACCCACTAGATGG[A/G]GCCAGTGTCTGCTTC | 5663 |
rs111240255 | snp | C/T | 0.021333 | 0.101051 | intron-variant | PSEN1 | GRCh38.p7 | 14:73199228 | AGTTGATATTTGAGA[C/T]AGAGACTTGAAGAAC | 5663 |
rs111319748 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73161594 | TCCAGGAGACACCCC[A/T]GGCTCAAGCTGTCAA | 5663 |
rs111323647 | snp | C/T | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210431 | ACTAAAGGATGAGAC[C/T]TAATGCTTTATCTTC | 5663 |
rs111444007 | snp | A/C | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73144627 | TAAGCAAGTGAACTT[A/C]TGTGTGCCACACTGT | 5663 |
rs111470957 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73184151 | GGCTGGCCGGCCGGG[A/G]GGCTGACCCCCCCAC | 5663 |
rs111471856 | snp | C/T | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73149931 | AATACTGTGACGAGC[C/T]GCTATAGCCTGGAAA | 5663 |
rs111475952 | snp | A/G | 0.17461 | 0.238362 | intron-variant | PSEN1 | GRCh38.p7 | 14:73165744 | CAAGAGTGAAACTCC[A/G]TCTTAAAAAAAAAAA | 5663 |
rs111557056 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197058 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 5663 |
rs111607475 | snp | A/T | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73216773 | CAAAAAAAAAAAAAA[A/T]ATTAATTAATATGAT | 5663 |
rs111650497 | in-del | -/T | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160604 | TCCTAACGGGTGTAG[-/T]TTTTTTTTTGCATTT | 5663 |
rs111657154 | snp | A/C | 0 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217010 | CCTAATTTTGTATAT[A/C]ATTTACTGACTTCTC | 5663 |
rs111694806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152675 | ATTCTTATGTTCTTA[C/T]TGGTAATTGGAGTTT | 5663 |
rs111704578 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141619 | TGAAACCCCCATCTC[A/T]ACTAAAAATACAAAA | 5663 |
rs111759355 | snp | C/T | 0.5 | 0 | missense | PSEN1 | GRCh38.p7 | 14:73211883 | GCTCTACACCTGAGT[C/T]ACGAGCTGCTGTCCA | 5663 |
rs111840015 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135553 | TTTTGTATTTTTAGT[A/G]GAGACGGGGTTTCAC | 5663 |
rs111945130 | snp | A/G | 0.0240643 | 0.107019 | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136715 | GGGCGGGGCGCGGCC[A/G]GTTGGGGCTGGGGAA | 5663 |
rs112024830 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200278 | TGAAATTAATCTTTT[G/T]TGTGTGTGTGTGAGA | 5663 |
rs112089114 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73205404 | GAATGGCGTGAACCC[A/T]GGAGACGGAGCTTGC | 5663 |
rs112101802 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | PSEN1 | GRCh38.p7 | 14:73164985 | TTTTTGAGACGGAGT[C/G]TCATTCTGTCACCCA | 5663 |
rs112249292 | snp | C/G | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157842 | AATGCAAAAATTAGC[C/G]AGGGGTGGTGGCGTG | 5663 |
rs112287075 | snp | C/T | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141388 | GCTGCTTTCACAAAG[C/T]CTTTTATAGGGCTGG | 5663 |
rs112451138 | snp | C/T | 0.5 | 0 | missense | PSEN1 | GRCh38.p7 | 14:73192667 | TTAAAACCTATAACG[C/T]TGCTGTGGACTACAT | 5663 |
rs112456911 | snp | A/T | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73217413 | CTCTACCCTGGCCAC[A/T]CATTAGAATCACTTG | 5663 |
rs112516950 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73183024 | TCCCACTGGTATTGT[G/T]TGTCTTGGCCAAGAC | 5663 |
rs112549106 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PSEN1 | GRCh38.p7 | 14:73161141 | CACCATACCCACCTA[A/G]TTTTTGTATTTTTTG | 5663 |
rs112560505 | snp | A/G | 0.0810805 | 0.184299 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193491 | TGAAGTGGAGGTTGC[A/G]GTGAGCCGAGATGGT | 5663 |
rs112592871 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73197180 | CCTTGTGATCCGCCC[A/G]CCTCGGCCTCCCAAA | 5663 |
rs112724703 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186252 | GGTGTGGTGGCACAT[G/T]TCTGTAATCCCAGCT | 5663 |
rs112850015 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73183921 | GGCGGCTGGCCGGGC[G/T]GGGGGCTGACCCCCC | 5663 |
rs112890654 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148321 | CACATATCACCACCT[C/T]AGTTGAAGCCTTCTC | 5663 |
rs112911413 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219738 | AACCCAATAATTCTG[C/T]ATTAACTGAATTCTG | 5663 |
rs113020306 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73193547 | AGAGCGAGACTCTGT[C/G]TCAAAAAAAAAAAAA | 5663 |
rs113071478 | snp | A/C | 0.5 | 0 | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73224054 | AAATCTGTTTATAAA[A/C]GCCCCAAAGCAGCTA | 5663 |
rs113074873 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134674 | GGATTACAGGCATGC[A/G]CCACCACGCCTGGCT | 5663 |
rs113120089 | snp | A/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73201085 | TATCTTTTTGTTTGT[A/T]TGTTTGTTTGTTTGT | 5663 |
rs113149216 | snp | A/G | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73155928 | TGTCAATGTAGGTTC[A/G]TCTGTTGTAACGGTT | 5663 |
rs113170743 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73140345 | CCTCCCGAGTAGCTG[A/G]GACTACAGGCGTGTG | 5663 |
rs113270982 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198748 | AAGCTTGAAGGAAAG[G/T]TGATGAAGAAAAAAT | 5663 |
rs113332832 | snp | A/T | 0.0322114 | 0.122752 | intron-variant | PSEN1 | GRCh38.p7 | 14:73146844 | ACACGGATTTTTGCC[A/T]TCTATATTTCTGAAA | 5663 |
rs113386556 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141717 | TTGAACCCAGGAGGT[A/G]GAAGTTGCAGTGAGC | 5663 |
rs113426609 | snp | A/G | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201669 | ATTCCTGTCTCACAG[A/G]CAGAGCAGGTGGTGA | 5663 |
rs113449244 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186654 | TGGTGGCGCGCACGC[A/C/G]TGGTTCCACCTACTC | 5663 |
rs113485120 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171139 | GCCTCTGCATTGAAG[A/G]GGCATGACTTAGCTG | 5663 |
rs113494605 | snp | C/T | 0.00676609 | 0.0577691 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134955 | TCCTATTAATATTAG[C/T]GGACTGCAATCAGAT | 5663 |
rs113643130 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73191608 | GCTGGAGTGCAGTAG[C/T]GTGATCATAGCTCAC | 5663 |
rs113733863 | snp | A/G | | | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134586 | AGGCTGGAATGCAAT[A/G]GCGCAATCTCGGTTC | 5663 |
rs113749630 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136680 | GCCCGGGCCGCGAAG[C/T]CGGTGTCCTAAAAGA | 5663 |
rs113774566 | snp | C/T | 0.147991 | 0.228242 | intron-variant | PSEN1 | GRCh38.p7 | 14:73189070 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGTGCC | 5663 |
rs113832178 | in-del | -/TTCA | 0.5 | 0 | intron-variant | PSEN1 | GRCh38.p7 | 14:73164877 | TCATATATATATATG[-/TTCA]TTCATAAATTAAATC | 5663 |
rs113901631 | snp | A/G | 0.147656 | 0.228091 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208221 | GCAAGTGGGGGGCAC[A/G]TTTCAGCCCTGTTTG | 5663 |
rs113937326 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205209 | AGGCCGGGCGTGGTG[G/T]CTCACGCCTGTAATC | 5663 |
rs113972466 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167116 | TTCAGCTCATGGTTC[G/T]TGAGGCTGGAAAGCC | 5663 |
rs113991031 | snp | A/G | 0 | 0 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219652 | ACTCTCAGGACTACC[A/G]TTACCAAGAGGTTAG | 5663 |
rs113994990 | snp | C/T | 0.0441095 | 0.141807 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135732 | GATACCATGTACCGT[C/T]AATTTCATTTTCGGT | 5663 |
rs114000457 | snp | C/T | 0.0444908 | 0.142359 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222926 | GAATTTGGAAGGAGA[C/T]GTGAAAATTGGACAT | 5663 |
rs114004599 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158169 | AGATAGTGGCTGTTA[C/T]GGATATTCATGTACA | 5663 |
rs114014192 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204597 | TTTACTCCCTGGCCA[C/T]TTACAGAAAAAGTTA | 5663 |
rs114017123 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210738 | AAAATTGTGAGGGCT[C/T]TCCCAGAGGAAGCCA | 5663 |
rs114229922 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143130 | ATTGACCGCCATGCA[A/G]TCCTCAATTGTTTTC | 5663 |
rs114285804 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204382 | TGAAATGAAAAGTGA[C/T]TTTTAAAAAAATATT | 5663 |
rs114317083 | snp | A/G/T | 1.73851e-05 | 0.00294826 | missense | PSEN1 | GRCh38.p7 | 14:73198069 | AAAGGTCCACTTCGT[A/G/T]TGCTGGTTGAAACAG | 5663 |
rs114336572 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | PSEN1 | GRCh38.p7 | 14:73159352 | GCACCCAGCTAATTC[C/T]GTTTGTATTTCATTG | 5663 |
rs114378630 | snp | C/T | 5.28062e-05 | 0.00513812 | missense | PSEN1 | GRCh38.p7 | 14:73198103 | AGGAGAGAAATGAAA[C/T]GCTTTTTCCAGCTCT | 5663 |
rs114386278 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198725 | TAGCAACTGAGGAGA[A/G]AAGTTGTAAGCTTGA | 5663 |
rs114445862 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201059 | ATCCCCACCCTCCCA[A/G]AAAAAGAGAATATCT | 5663 |
rs114467135 | snp | C/G | 0.0345262 | 0.126772 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212512 | CAGTAAGCCTTCATG[C/G]CCGTAATACATTTGT | 5663 |
rs114498425 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160362 | AAGTGGCTATGCACA[G/T]ATCTGTTTGAGGTCT | 5663 |
rs114499894 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198349 | AAGAAAGAAAATGTT[C/T]AGATATTGGGGAACC | 5663 |
rs114576149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157511 | CATACTTAAAGTATA[C/T]AGTGTGATGTTTTGA | 5663 |
rs114615055 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186071 | AACAACTTTGTTGTA[C/T]CTGGATATAATTTAG | 5663 |
rs114616749 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | PSEN1 | GRCh38.p7 | 14:73215957 | CCAGGAGTCTACCCA[A/G]TGGAAATGAAAACAG | 5663 |
rs114634160 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73209708 | ATAGGGGAATTTTAC[A/G]TATCCTGGAAAGTCA | 5663 |
rs114653436 | snp | A/C | 0.0345262 | 0.126772 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210894 | ATTTTAATTATTTTT[A/C]ATGTATGGAAGTTTT | 5663 |
rs114679458 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171433 | ATATATAAAGTTTTG[A/G]TGCCGCAAAAGAAGT | 5663 |
rs114776088 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | PSEN1 | GRCh38.p7 | 14:73150445 | TACATAAATCGTATC[A/G]CATTATGTAATACAC | 5663 |
rs114782352 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154909 | CTGAGGTTGTAGGGA[A/G]ATAGGCTTTCTTGTA | 5663 |
rs114944042 | snp | A/G | 0.183942 | 0.241115 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160035 | CGCCATATTGGCCAG[A/G]CTGATCTCAAACTCC | 5663 |
rs114952061 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197273 | AATGAAAGAAAAAGT[A/G]CAGTTGATCGAAAGA | 5663 |
rs115076395 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195651 | GGCTGGAGTGAAGTG[A/G]CACGATTATAGCTCA | 5663 |
rs115123722 | snp | A/G | 0.185472 | 0.241529 | intron-variant | PSEN1 | GRCh38.p7 | 14:73150610 | CTACTAAAAAAAAAT[A/G]CAAAATTTAGCCAGG | 5663 |
rs115164402 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | PSEN1 | GRCh38.p7 | 14:73190233 | TGGCTCACACTTGTA[A/G]TCTCACCTATTTGGG | 5663 |
rs115322640 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PSEN1 | GRCh38.p7 | 14:73193822 | CCACCATGCCTGACT[A/G]ACTTGTTTATTTTTT | 5663 |
rs115334263 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PSEN1 | GRCh38.p7 | 14:73175168 | TCTCGCTCTTGTCCC[A/G]CAGGCTGGAGTGTGA | 5663 |
rs115376785 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211461 | CCAAGTTACAACCCC[A/G]CAACCTTAGAGCTTT | 5663 |
rs115546755 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212504 | AATTGTTCCAGTAAG[C/G]CTTCATGGCCGTAAT | 5663 |
rs115555746 | snp | A/C/G | 0.0452528 | 0.143452 | intron-variant | PSEN1 | GRCh38.p7 | 14:73140921 | TCCTTGTAGGTAGAT[A/C/G]TGTGGATCGGTGAGG | 5663 |
rs115620087 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PSEN1 | GRCh38.p7 | 14:73142248 | AGGGAGAAGCTTTCA[A/G]AGTAACACTGAGGCT | 5663 |
rs115697938 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171770 | AAAACATTGCTTTAC[A/G]AGGAAGTTAAGTTTA | 5663 |
rs115702167 | snp | C/T | 0.0966517 | 0.197444 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196712 | ACTCCTGAGCACAAG[C/T]GATCTGCTGCCTCAG | 5663 |
rs115717679 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169384 | TCATCCATTTCTGAG[A/G]CCTGAGATTTCATCC | 5663 |
rs115739628 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PSEN1 | GRCh38.p7 | 14:73214089 | AACCCACATGTCTAT[C/T]AACTGATAAGTGGAT | 5663 |
rs115760359 | snp | A/G | 0.000362337 | 0.013455 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73192749 | TCACTGGAAAGGTCC[A/G]CTTCGACTCCAGCAG | 5663 |
rs115865530 | snp | A/G | 0.000268939 | 0.011593 | missense | PSEN1 | GRCh38.p7 | 14:73206449 | AAAGGAGAGTATCCA[A/G]AAATTCCAAGTATAA | 5663 |
rs115882151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73218627 | ACGGAGGAGCCTGTG[C/T]GGGAAGAATGCTCCC | 5663 |
rs115891135 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205820 | ATATCTAGATCTAGA[C/T]TGATATATTGATATA | 5663 |
rs115909396 | snp | A/C/G | 0.0520825 | 0.152737 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152769 | AAATATTCGCTGGGC[A/C/G]TGGTGGCTCACGCCT | 5663 |
rs116061552 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198859 | GCTCACTGCAGCCTC[A/G]ACCTCCCAGGCTCAG | 5663 |
rs116107724 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | PSEN1 | GRCh38.p7 | 14:73177030 | TTTCTGGACCTTATT[A/G]CCATTTGACTTATTT | 5663 |
rs116226928 | snp | A/G | 0.102726 | 0.202016 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152946 | TACCTGGGAGGCTGA[A/G]GCAAGAGGATTGGTT | 5663 |
rs116296065 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PSEN1 | GRCh38.p7 | 14:73146764 | GTGAAAATGAAATAG[A/G]ACATTGAGAAAATTT | 5663 |
rs116300507 | snp | A/G | 0.0444908 | 0.142359 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73136226 | CACACGCTGGGCCCA[A/G]TTTATATAGGGGCTT | 5663 |
rs116314689 | snp | A/G | 1.64857e-05 | 0.00287099 | missense | PSEN1 | GRCh38.p7 | 14:73170893 | GGTAACTCCCGGCAG[A/G]TGGTGGAGCAAGATG | 5663 |
rs116321567 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | PSEN1 | GRCh38.p7 | 14:73164503 | GACACCGTGAGATAC[A/G]TCTTTGAAGTACTAT | 5663 |
rs116395726 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208202 | TCTCGCCACCTGCAA[C/T]GTGGCAAGTGGGGGG | 5663 |
rs116426584 | snp | A/G | 0.0444908 | 0.142359 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135761 | GTTTTTTGAATACCC[A/G]TGTTTGACATTTCTC | 5663 |
rs116442941 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152762 | AAAAAAGAAATATTC[A/G]CTGGGCATGGTGGCT | 5663 |
rs116443630 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210214 | AGTCATAGATAATAA[C/T]ATAAAATTCATCAGT | 5663 |
rs116466962 | snp | A/G/T | 0.000215693 | 0.0103831 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73148040 | AGAGTTACCTGCACC[A/G/T]TTGTCCTACTTCCAG | 5663 |
rs116521228 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141761 | TTGCATTCCAGCCTG[A/G]GCGACAAGAGTGAAA | 5663 |
rs116616518 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PSEN1 | GRCh38.p7 | 14:73209992 | CAATAATCAAAAACT[A/C]CTCCATCCTAGTTAT | 5663 |
rs116640707 | snp | C/T | 0.000445276 | 0.0149144 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73211815 | AGAGAATGATGATGG[C/T]GGGTTCAGTGAGGAA | 5663 |
rs116825425 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73202231 | TTTTTTCCATATTTT[C/T]AGTTGAGCCACAGGT | 5663 |
rs116882898 | snp | C/T | 0.000297044 | 0.0121833 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73170847 | ACGGAGCCTTGGCCA[C/T]CCTGAGCCATTATCT | 5663 |
rs117170264 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | PSEN1 | GRCh38.p7 | 14:73166183 | TCATTATCAGCCTTG[A/G]GCAGGGCAGGGTTGA | 5663 |
rs117236337 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PSEN1 | GRCh38.p7 | 14:73215476 | TAATCCCAGCTATTC[A/G]AGAGGCTGCGGCAGG | 5663 |
rs117394753 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221869 | GTGCCTTCACTCACA[C/T]GGGACAGGCGGTGGT | 5663 |
rs117414600 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198270 | CCTGCAGATCTCTTT[G/T]TTTCCTTGCAAGCAA | 5663 |
rs117484602 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PSEN1 | GRCh38.p7 | 14:73175694 | TTACTTCTCAAATGT[C/T]CCTGATGTTGGACAT | 5663 |
rs117490301 | snp | G/T | 0.0633504 | 0.166319 | intron-variant | PSEN1 | GRCh38.p7 | 14:73153528 | GCATGTTCCCTATGA[G/T]TAATAAATGTTTTCA | 5663 |
rs117563918 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PSEN1 | GRCh38.p7 | 14:73149199 | TAAAAAGAACTTTCT[C/T]ATAGCCTGGCATGGT | 5663 |
rs117636016 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | PSEN1 | GRCh38.p7 | 14:73202191 | TTGAGATTACAAGCA[C/T]GCGCCACTATACCTG | 5663 |
rs117643810 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187219 | AATGTTTTAAGAAAG[A/G]GTTTTAAGAATGTAT | 5663 |
rs117826622 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73209118 | GGGGCTTCCTGGACC[C/T]CTGAGAGCACAGGGA | 5663 |
rs117869781 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | PSEN1 | GRCh38.p7 | 14:73202224 | TAATTTTTTTTTTCC[A/G]TATTTTTAGTTGAGC | 5663 |
rs117973146 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186490 | TTGTTTTAAAGAGAG[A/G]TGTGGGCCGGGCATA | 5663 |
rs118079222 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168847 | TCCCCGAATGGCCGC[A/G]TTGAAGGAGCATTGA | 5663 |
rs118140704 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | PSEN1 | GRCh38.p7 | 14:73176728 | TGTTTTAATTAAACA[C/T]TAGTTCTTTGAGGTA | 5663 |
rs118144727 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | PSEN1 | GRCh38.p7 | 14:73149802 | ATTGTTGTTTAACTT[A/C]GAGTACTATTACAGT | 5663 |
rs121917807 | snp | A/G | | | missense | PSEN1 | GRCh38.p7 | 14:73198057 | GTTTTGTGTCCGAAA[A/G]GTCCACTTCGTATGC | 5663 |
rs121917808 | snp | A/C | | | missense | PSEN1 | GRCh38.p7 | 14:73219192 | CATTGCCAGCTCTTC[A/C]AATCTCCATCACCTT | 5663 |
rs121917809 | snp | A/G | 0.000230597 | 0.0107352 | PSEN1 | 14 | allele_origin=G(germline)/A(germline) | 14:73211811 | TTGCAGAGAATGATG[A/G]TGGCGGGTTCAGTGA | 5663 |
rs137863233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73161372 | TAGGCCCATTTGTCT[A/G]TTTTTGTTTTTGTTC | 5663 |
rs137920817 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157499 | ACGTAAAATGTACAT[A/C]CTTAAAGTATACAGT | 5663 |
rs137921477 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201005 | ACAGTGAGCCATGAT[C/T]GTGCCACTGCACTCC | 5663 |
rs137925118 | in-del | -/CACAA | 0.00119737 | 0.0244387 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223032 | ACCTCTTTAAATTCC[-/CACAA]CACAAGAGATTAAAA | 5663 |
rs137925179 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194122 | ACTCCAGCCATTAAC[C/T]CAGGCAGCTTTCAGG | 5663 |
rs137926268 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148629 | CAACTCTACTAGCTA[A/G]TCATCATAAAGTGAG | 5663 |
rs138061744 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135757 | TTCGGTTTTTTGAAT[A/C]CCCATGTTTGACATT | 5663 |
rs138119474 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211498 | GAAGAGGCTTGGTGG[G/T]ATTACCGTGCTTGGC | 5663 |
rs138178179 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169412 | TCCATTTCTGAGGCT[A/G]TAGAGACCAGTGACT | 5663 |
rs138181695 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198544 | CAGCACTGTGTGAGA[C/T]GAATTGGTGGGTTGG | 5663 |
rs138205623 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201760 | TTTATTTATTTATTT[A/T]TTTTGAAACAGAGTC | 5663 |
rs138245461 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148192 | AATGCTGAGGGGGCT[A/G]GGCAGGCTTTCTCTA | 5663 |
rs138247564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143110 | GCTGCCTGAACAGTG[A/G]GGTCATTGACCGCCA | 5663 |
rs138311229 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PSEN1 | GRCh38.p7 | 14:73183146 | TTTTTGAGATGGAGT[C/G]TCGCTCTGTTGCTCA | 5663 |
rs138312917 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73172915 | GGGGAGAAAAGAACA[C/T]AGGACATGTCAGCAG | 5663 |
rs138396026 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195218 | CGCTTTGTTGCCCAG[A/G]CTGGAGTGCAGTGGC | 5663 |
rs138425111 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73189561 | AGGTTGCTGTGAGCC[A/G]AGATCGCACCATTGC | 5663 |
rs138479907 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | PSEN1 | GRCh38.p7 | 14:73212347 | AACTCCTGACATCAT[A/G]ATCTGCCTGCCTTAG | 5663 |
rs138527450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73178565 | TGTTTATTTTCCAAT[C/T]TTTTTCACTATTGTT | 5663 |
rs138601588 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73199181 | ACATTGCTAGCAGAC[A/G]TTTAGAAATGAAATA | 5663 |
rs138620990 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221832 | TGTCACTGGAAAGAA[C/T]AGTAGCAATTTCCAT | 5663 |
rs138638872 | snp | A/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135206 | CCTTCTCCCACAACT[A/T]ATCTTTCATTCTGCT | 5663 |
rs138678883 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PSEN1 | GRCh38.p7 | 14:73165081 | CCTGCCTCAGCCTCC[C/T]AAGTAGCTGAGATTA | 5663 |
rs138683430 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PSEN1 | GRCh38.p7 | 14:73177495 | CTATGCCAGGACAGC[C/T]GTTTTCTTCTAGTAT | 5663 |
rs138686510 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168938 | CAACTGGCTGGTTCC[C/T]GCATTCGTTTGCTCT | 5663 |
rs138803782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139921 | TGTTTAAGTTGATCA[A/G]AGCAAAAGAAAGACT | 5663 |
rs138852262 | in-del | -/TAC | 0.0103295 | 0.0711199 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196252 | ATAAAACTGAAATAG[-/TAC]TACTGAATGTGGCAG | 5663 |
rs138855796 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PSEN1 | GRCh38.p7 | 14:73165727 | CACTCCAGCCTGGGC[A/G]ACAAGAGTGAAACTC | 5663 |
rs138871096 | snp | A/G | 3.29908e-05 | 0.00406132 | missense | PSEN1 | GRCh38.p7 | 14:73211816 | GAGAATGATGATGGC[A/G]GGTTCAGTGAGGAAT | 5663 |
rs138902912 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221685 | AGCCTGAGTAGCTGA[A/G]ACTACAGCCCATCTT | 5663 |
rs138907808 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205203 | GTGACCAGGCCGGGC[A/G]TGGTGGCTCACGCCT | 5663 |
rs138923281 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162175 | CAGGAGCAAAACTCC[A/G]TCTCAAAAAAAAAAA | 5663 |
rs138972350 | in-del | -/TA | 0.0444908 | 0.142359 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197704 | CTGCTTAAAATAGTC[-/TA]TCTCATCATTATCTC | 5663 |
rs138973092 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152780 | GGGCATGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 5663 |
rs139004553 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73177384 | TTGCTGGGGTTTTTT[-/T]GTGTGTGTGTTTTTG | 5663 |
rs139048521 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PSEN1 | GRCh38.p7 | 14:73144943 | TGTCACCCAGGCTGC[A/G]GTGCAGTGGCGCAAT | 5663 |
rs139058678 | in-del | -/T | 0.0807149 | 0.183963 | intron-variant | PSEN1 | GRCh38.p7 | 14:73164658 | TAAATCCTGGTAGTC[-/T]TGACCCCAGAACTTG | 5663 |
rs139071886 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73147616 | TGGTGTCTCAGGCGG[G/T]TCTACTTATTGCTAA | 5663 |
rs139085364 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | PSEN1 | GRCh38.p7 | 14:73175213 | CTCACTGCAAGCTGT[A/G]CCTCCTGGGTTCAAG | 5663 |
rs139112977 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | PSEN1 | GRCh38.p7 | 14:73142423 | AACAAGCCACAAGCC[A/C]TTTGTGCTAGAGATC | 5663 |
rs139222371 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | PSEN1 | GRCh38.p7 | 14:73150605 | TGTCTCTACTAAAAA[A/G]AAATGCAAAATTTAG | 5663 |
rs139224866 | snp | A/G | | | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219574 | ATATGATAGGCCCGG[A/G]AGTTGCTGTGCCCCA | 5663 |
rs139255158 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197057 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 5663 |
rs139391117 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PSEN1 | GRCh38.p7 | 14:73209591 | TGTGGAGCTTATAGT[C/T]TATTTGGAGAGATAG | 5663 |
rs139392169 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73180283 | AGCCACCACGCCCAG[A/C]CTTATCCTTCATTTT | 5663 |
rs139503683 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | PSEN1 | GRCh38.p7 | 14:73142045 | GCACTCCAGCCTGGG[C/T]GACAGAGGGAGACTC | 5663 |
rs139521885 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204084 | GCTCACCACAGCCTC[C/T]GCCTCCTGGATTCAA | 5663 |
rs139537733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73166341 | CATAGAAAGAAAACA[A/G]GTTTTGAGGCAAGAG | 5663 |
rs139574327 | snp | A/C/G | 0.00279162 | 0.0372561 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223121 | AACAAAGCTGTCATC[A/C/G]GGCTCACAGCTCAGA | 5663 |
rs139669544 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192072 | CCATTTATATGAATG[A/G]TACAGAGCTTCCTAT | 5663 |
rs139695161 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73159354 | ACCCAGCTAATTCCG[C/T]TTGTATTTCATTGAT | 5663 |
rs139756175 | in-del | -/G | | | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73223801 | AATTAGCCAGGCGTG[-/G]GTGGTGGGCGCCTGT | 5663 |
rs139863395 | snp | C/G | 0.000939532 | 0.0216537 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73171030 | AGTCAGCTTTTATAC[C/G]CGGAAGGATGGGCAG | 5663 |
rs139870552 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant | PSEN1 | GRCh38.p7 | 14:73155287 | ATGATCTTTGGCAAA[-/T]TTAACTGGCCTCGCT | 5663 |
rs139941526 | snp | C/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73187313 | TCAAATGAAATCTTA[C/T]ATGAAATTTTCATAT | 5663 |
rs139953121 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73213884 | CTGGAATCCTCATAC[A/G]CTGCTGGTGGGAATG | 5663 |
rs139961867 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169835 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 5663 |
rs139964536 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145686 | TGAACTTGTATGGAT[A/T]CTCAAAAAGTACAGT | 5663 |
rs140012487 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223401 | TTTCCTTTTGAAATA[C/T]GTAATTGTTGAGACT | 5663 |
rs140027376 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | PSEN1 | GRCh38.p7 | 14:73202693 | TAGCCAGGATTGTCT[C/T]GATCTCTTGACCTCG | 5663 |
rs140064975 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | PSEN1 | GRCh38.p7 | 14:73192748 | TTCACTGGAAAGGTC[C/T]ACTTCGACTCCAGCA | 5663 |
rs140082086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198323 | TCAAGAGAGTTTTCA[A/G]TATGAATAGAAAGAA | 5663 |
rs140089088 | snp | A/G | 0.00525956 | 0.0510109 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171086 | ATTCTCAAAGCCAGT[A/G]TGGCTTTTCTTTACA | 5663 |
rs140164309 | snp | C/G | 0.0955749 | 0.196603 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200377 | CAGGTTCAAGCAATT[C/G]TCCTCTCTCAGCCTC | 5663 |
rs140169796 | snp | C/T | 1.64743e-05 | 0.00287 | missense | PSEN1 | GRCh38.p7 | 14:73219248 | GATTATCTTGTACAG[C/T]CTTTTATGGACCAAT | 5663 |
rs140189461 | snp | C/G/T | 6.60715e-05 | 0.00574736 | missense | PSEN1 | GRCh38.p7 | 14:73170833 | GAGCACAACGACAGA[C/G/T]GGAGCCTTGGCCACC | 5663 |
rs140238059 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | PSEN1 | GRCh38.p7 | 14:73174337 | CCACCAGTTTCAAGC[A/G]ATTCTCCTGCCTCTG | 5663 |
rs140346058 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73172593 | CTGTGGCTGCTTTCA[C/T]ACTACAGTAGCACAG | 5663 |
rs140366572 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | PSEN1 | GRCh38.p7 | 14:73209988 | TTTGCAATAATCAAA[A/C]ACTCCTCCATCCTAG | 5663 |
rs140372057 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206883 | ATAAGTAAACAAAAA[A/C]AGCAAAATATAAACA | 5663 |
rs140447679 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205873 | ACAGAGGAGGCCTCT[C/T]GACTATCCCTATTAT | 5663 |
rs140461257 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157670 | ACCATGTTTTGTCAC[C/T]GCGCGCAGCCATTTA | 5663 |
rs140481942 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210884 | TCACTTATATATTTT[A/C]ATTATTTTTAATGTA | 5663 |
rs140525811 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PSEN1 | GRCh38.p7 | 14:73155299 | CAAATTAACTGGCCT[C/T]GCTAAACTTCAGTTT | 5663 |
rs140584670 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73147698 | ACAAATTAATACATT[A/C]CTGGTTTACAAATTG | 5663 |
rs140628433 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73209099 | TCGGAGCCTGCAGAC[A/G]CAAGGGGCTTCCTGG | 5663 |
rs140669416 | snp | G/T | 0.0948562 | 0.196037 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157196 | AGTGGCATGATCTTG[G/T]CTCACTGCAACGTCT | 5663 |
rs140707110 | in-del | -/ATC | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73144033 | TTTGCATTATAGCTT[-/ATC]TTTTTTTTTTTTTTT | 5663 |
rs140710323 | snp | A/T | 0.0221141 | 0.102801 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134697 | GCCTGGCTAACTTTT[A/T]TTGTATTTTTAGTAG | 5663 |
rs140717635 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PSEN1 | GRCh38.p7 | 14:73209208 | CCACCAACTCAGAAG[A/G]GGGCAGGACTCCCGC | 5663 |
rs140746584 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73159512 | TGATTGTTATACGTG[A/G]TCCAAGGTATGGATC | 5663 |
rs140763414 | in-del | -/TC | 0.0337553 | 0.125452 | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73224042 | GAGTGTAATATTAAA[-/TC]TGTTTATAAAAGCCC | 5663 |
rs140797307 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PSEN1 | GRCh38.p7 | 14:73196274 | ATGTGGCAGAATCAA[A/G]CAAGTTGAAAATCTC | 5663 |
rs140863358 | snp | C/T | 0.00175238 | 0.0295486 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192607 | TTTTGGTGAAAATTA[C/T]TGTACATCTTTTAAA | 5663 |
rs140865740 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73172135 | ACTCTCTAGACTCCT[A/G]GGGGGCTATCATGTG | 5663 |
rs140943336 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PSEN1 | GRCh38.p7 | 14:73138161 | CCACAAGGTGATTAT[C/T]CCTATTTTAAATTTT | 5663 |
rs140971082 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73176978 | GGTTACCAGTTTTTC[C/G]TTTGGTCGTATCTGC | 5663 |
rs141000002 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208051 | GTGTTAACCTGGGGA[A/G]CACAGGGGCACCCAG | 5663 |
rs141114226 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152531 | AGAATTGCTTGAACC[C/T]AGGACTCAGAGGTTG | 5663 |
rs141117435 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221163 | AGGCAGTCACAGACA[G/T]GAAAAATAAGAGCTA | 5663 |
rs141138081 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168500 | GTGTTGGTGATACAA[C/G]TGGCTGAGCAGCGAG | 5663 |
rs141145106 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210369 | TAAAGCTGAATTTAA[C/T]ATAAGGTTATGGCAC | 5663 |
rs141165471 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PSEN1 | GRCh38.p7 | 14:73142648 | TTTTTAATAAACTTA[C/T]TGTGAGATTCTGAAC | 5663 |
rs141187583 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | PSEN1 | GRCh38.p7 | 14:73144647 | TGCCACACTGTTTTC[A/T]TCTGTAAAAGGATAA | 5663 |
rs141253181 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PSEN1 | GRCh38.p7 | 14:73201268 | AATTTTTGTATTTTT[A/G]GTAGCAACGGGGTTT | 5663 |
rs141287499 | in-del | -/ATTT | 0.0908922 | 0.192833 | intron-variant | PSEN1 | GRCh38.p7 | 14:73166993 | TTTATTTATTTATTT[-/ATTT]TGTTGTTGTCATTTG | 5663 |
rs141365251 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73190912 | AATATAAATATCTAC[A/G]TCGTCCAGAAATTTC | 5663 |
rs141411304 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PSEN1 | GRCh38.p7 | 14:73136878 | GCCGGGATTAGTAGC[C/G]GTCTGAACTGGAGTG | 5663 |
rs141457172 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197154 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTTG | 5663 |
rs141535751 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73220821 | AAAACACACAAACAG[C/T]CATCAGCCTGTGTGG | 5663 |
rs141545983 | in-del | -/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73138975 | CTGTCAAGAAAAAAA[-/G]AAAAAAAATGTAAAA | 5663 |
rs141552089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73174039 | ATGCATGGAATCTAT[A/G]TGTCATGAAAAAATT | 5663 |
rs141585352 | in-del | -/GGGGGGGGGA | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73158164 | TTACAGATAGTGGCT[-/GGGGGGGGGA]GTTACGGATATTCAT | 5663 |
rs141603925 | snp | C/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73189758 | TGCAAGCCCTGGACA[C/G]TGGTGAAGCAGAGAT | 5663 |
rs141655641 | in-del | -/A | 0.0437281 | 0.141251 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211552 | AGAGTCATGTGGGAG[-/A]GGGGTGGGAACCCAA | 5663 |
rs141656976 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73179069 | AGTTTCTTTCTTTCT[C/G]TGATCTCCATGTGGT | 5663 |
rs141675857 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | PSEN1 | GRCh38.p7 | 14:73182792 | TGCAGTGAGCCAAGA[C/G]CATGCTACTGCACTC | 5663 |
rs141689717 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73218473 | GCCGGGTGAAGACTT[C/T]CTAGTGTTTCCGTAA | 5663 |
rs141730494 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PSEN1 | GRCh38.p7 | 14:73165355 | CGATTCTGGCTCAAA[C/T]GAATTCCTAGGCTCA | 5663 |
rs141799841 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73222784 | TTATACATTGGTGTT[A/G]TAAAAGTGACTTGAT | 5663 |
rs141804925 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73219397 | CAAAGTCAAGATTCC[C/T]GGCTGGACTTTTGCA | 5663 |
rs141822345 | snp | C/G | 0.000153988 | 0.00877328 | missense | PSEN1 | GRCh38.p7 | 14:73211922 | CCAGCAGTATCCTCG[C/G]TGGTGAAGACCCAGA | 5663 |
rs141833880 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169438 | TGACTTCCTCTGACT[C/T]TTCTGAGCTTGAAAT | 5663 |
rs141974188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73209432 | AGCTAAAGAAAATCA[A/G]ATGATTGTCTGTGAG | 5663 |
rs142010550 | snp | C/G/T | 0.00318978 | 0.0398085 | intron-variant | PSEN1 | GRCh38.p7 | 14:73169083 | AGTCTCATCTCAATC[C/G/T]GACTTCCCTCTTCAC | 5663 |
rs142030001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168387 | AACAAAAAAGATTTC[A/G]GCAGCTGGGAGAACA | 5663 |
rs142053866 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73206322 | TGGAGAAATGATGGC[G/T]TGTTGTTGTCTATGC | 5663 |
rs142093869 | snp | C/G | 0.000153988 | 0.00877328 | missense | PSEN1 | GRCh38.p7 | 14:73173681 | ACTATCCTCCTGGTG[C/G]TTCTGTATAAATACA | 5663 |
rs142112766 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSEN1 | GRCh38.p7 | 14:73164600 | ACTGAAGTTCAAAGA[A/G]GTTAAATAACTCGCC | 5663 |
rs142189156 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73181939 | CCACCACGCCTAGCT[A/G]ATGTTCGTATTTTTA | 5663 |
rs142195160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73149521 | CTCTGAAGATTTAGG[A/G]TTCTTCACTTTTCCC | 5663 |
rs142207090 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PSEN1 | GRCh38.p7 | 14:73202991 | CTGTGTAGATCAGGT[A/T]GGTTCAAGATTGCAT | 5663 |
rs142234263 | in-del | -/AT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73175677 | TTCAAGTGCCTTGTA[-/AT]TTACTTCTCAAATGT | 5663 |
rs142323671 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73139587 | TCCATAAGAAAAAAA[A/G]AAAAAAAAGGGGGGC | 5663 |
rs142346467 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187984 | CCCAGGCTGGAGTGC[A/G]GTGGCATGATCTCGG | 5663 |
rs142355580 | in-del | -/T | 0.197082 | 0.244335 | intron-variant | PSEN1 | GRCh38.p7 | 14:73194239 | GCCATGGCCATACTC[-/T]TTTTTTTTTTCTTTT | 5663 |
rs142405996 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221733 | ATCTCAGGCAGAGAA[C/T]TTTTCCCTCAAACAT | 5663 |
rs142413545 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PSEN1 | GRCh38.p7 | 14:73150929 | AAAAATTAGCTGGGC[A/G]TGGTGACACGCGCCT | 5663 |
rs142429755 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152967 | AGGATTGGTTTCAAG[A/G]TTCACCTGGGAGGTC | 5663 |
rs142457921 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73224154 | TGTAAACTTATAAGA[C/T]GTATGTTGTACAGTG | 5663 |
rs142482786 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73147453 | TTGCAAAATTAAAAG[C/T]GCTAGACAAATGATT | 5663 |
rs142494111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73148660 | AGCAGAGGCCAGGCA[C/T]GGTGGCTCATGCCTG | 5663 |
rs142499364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73171656 | GCTAAACTAATTCCA[A/G]TTGGCTAATTTAAAG | 5663 |
rs142533546 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210230 | ATAAAATTCATCAGT[A/G]GAAAAAAATGAGGCA | 5663 |
rs142625534 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PSEN1 | GRCh38.p7 | 14:73186311 | TTGAACCCTGGAGGC[A/G]GAGGTTGCGGTGAGC | 5663 |
rs142638003 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PSEN1 | GRCh38.p7 | 14:73215952 | CACCCCCAGGAGTCT[A/G]CCCAATGGAAATGAA | 5663 |
rs142799518 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157917 | CTTGAACCCAGGAGG[C/T]AGAGGTTGCAGTGAG | 5663 |
rs142823714 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204937 | GCCCTTCAGTTTTTC[G/T]TCTTTAGATCTGGAT | 5663 |
rs142849869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73146480 | TTAATATGAATTTGC[A/G]TTTCGCTGATCTCAT | 5663 |
rs142868766 | snp | A/G | 0.163236 | 0.234461 | intron-variant | PSEN1 | GRCh38.p7 | 14:73202131 | CTCACTGCAACCTCC[A/G]TCTCCTGGGTTCAGG | 5663 |
rs142880209 | snp | A/C | 0.0441095 | 0.141807 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158720 | TCCCGCCTTGGCTTC[A/C]CAAAGTGCTGGGATT | 5663 |
rs142910718 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | PSEN1 | GRCh38.p7 | 14:73203319 | TCTCAAACTTGTGAC[C/T]TCAGGTGATCTACCC | 5663 |
rs142982254 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73163981 | ATGGACTAGGGGAGC[A/T]TAAAAGCAGAAAGAC | 5663 |
rs143121060 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PSEN1 | GRCh38.p7 | 14:73142861 | TTGAGCAAGTGTCTT[C/G]AGATTAAGAAAATGG | 5663 |
rs143124022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168685 | AGAACCACTTCCATC[A/G]TGCAATACAATCTTC | 5663 |
rs143206356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73209743 | GTGCTTCCCTGAGGA[A/G]GTGGTAATAGGGGAC | 5663 |
rs143229105 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73173865 | ACTGTGGAACATTCA[A/G]AAAATACAAAAAGGA | 5663 |
rs143258167 | snp | C/G | 0.0356815 | 0.128715 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187987 | AGGCTGGAGTGCAGT[C/G]GCATGATCTCGGCTC | 5663 |
rs143344129 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143676 | GTTTCTTGTAATAAC[C/T]GAACAGATCCTGTTA | 5663 |
rs143357125 | snp | C/G/T | 0.00279258 | 0.0372817 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210514 | TGAGCATGCTACTTA[C/G/T]AATTAATTATGGAGG | 5663 |
rs143439617 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73176019 | CATTTAGTTGGTTAC[C/T]AGTAATATCACATAC | 5663 |
rs143503368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73213948 | GTAGTTCTTTGAAAG[A/G]TTAAATATGACCCGG | 5663 |
rs143537248 | in-del | -/GGTGG | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73194153 | ACGTACTCTGTGGCT[-/GGTGG]GTTGCCTTGTATGAA | 5663 |
rs143587069 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162928 | TACCTTTTAATACTT[C/T]CTTTGAGACCATGTG | 5663 |
rs143606369 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PSEN1 | GRCh38.p7 | 14:73165270 | CCAAACTGTGCTTTT[A/T]TTAAATAAAGAAATT | 5663 |
rs143622535 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | PSEN1 | GRCh38.p7 | 14:73195611 | TTTTTCTGTTTTAAG[A/T]AACAGGATCTCACTC | 5663 |
rs143648541 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PSEN1 | GRCh38.p7 | 14:73140747 | AAAGTTACAGATAAG[A/G]GATTCTGGACTTGCG | 5663 |
rs143683769 | snp | A/C | 0.000153988 | 0.00877328 | missense | PSEN1 | GRCh38.p7 | 14:73211880 | ATCGCTCTACACCTG[A/C]GTCACGAGCTGCTGT | 5663 |
rs143702018 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73157500 | CGTAAAATGTACATA[C/G]TTAAAGTATACAGTG | 5663 |
rs143763464 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PSEN1 | GRCh38.p7 | 14:73198914 | GAGTAGCTGTGACTA[C/T]AGGCACGCACTACCA | 5663 |
rs143782428 | snp | C/T | 0.000313126 | 0.0125086 | synonymous-codon | PSEN1 | GRCh38.p7 | 14:73170943 | GACATTGAAATATGG[C/T]GCCAAGCATGTGATC | 5663 |
rs143783639 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | PSEN1 | GRCh38.p7 | 14:73197224 | AGGCGTGAGCCACTG[C/T]GCCCGGCCTATATGC | 5663 |
rs143795534 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152158 | ACCTCGTGATTCGCC[C/T]GTCTCGGCCTCCCAA | 5663 |
rs143844465 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PSEN1 | GRCh38.p7 | 14:73143436 | TACACTCTCTCTGTA[A/G]CTCTGTGCAGGCAAA | 5663 |
rs143856904 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73175609 | ACTTTGGTGTGAACA[G/T]TTTTTCTATTATAAA | 5663 |
rs143861413 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73159443 | TTTCCTGCATTTTCT[G/T]CTGGAAGCTTTATAG | 5663 |
rs143891048 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73190460 | TGCCCTCTATCCAGG[G/T]TGACAGTCAGACCTT | 5663 |
rs143926761 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200475 | GGATTTCACCACGTT[A/G]GCCAGGCTGGTCTCA | 5663 |
rs143988789 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145324 | TCCATAATGGAGTGT[A/C]CTTTTATTATTTTAT | 5663 |
rs143989467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73174738 | ACTGGTGACTGGTCA[C/T]ACCTTGCCTAAACTG | 5663 |
rs144066042 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73141035 | GCAGAAGTACAAGAA[C/G]TCAAGGCCAACTGCA | 5663 |
rs144084598 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73176490 | CCTGCCTTTCCCTTA[A/C]AAAATACCTGTGTAG | 5663 |
rs144123666 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73142530 | AAATGGAATCAATAA[A/G]TAACCATGTTCTGCA | 5663 |
rs144133432 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73137265 | CGGTGGTGGCAGAGG[C/G]TTACAAGAAACACTA | 5663 |
rs144157631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73180734 | TGTTTTCTTTCATAC[C/T]CTTTAGCACAGGAAA | 5663 |
rs144291400 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73162655 | CAGAGAATCTGTCTC[A/C]AAGATAAGAAGAATG | 5663 |
rs144330235 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PSEN1 | GRCh38.p7 | 14:73168422 | AAGCAGCTGACGTCA[A/G]GGATATAAATGGCTG | 5663 |
rs144330434 | in-del | -/T | 0.0633504 | 0.166319 | intron-variant | PSEN1 | GRCh38.p7 | 14:73211360 | GAAGGGGACTGTTTA[-/T]TTTTTTCCTTTAGTC | 5663 |
rs144396262 | snp | A/C | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73167222 | GTAACAAAGTCACTC[A/C]CATGATAACTAACCT | 5663 |
rs144417985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73210023 | TTCCAAACACTCCCC[A/G]GAAGGGAGGTGCTAT | 5663 |
rs144455736 | snp | A/C | 0.00636936 | 0.0560724 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73223230 | GGTGCTGAAATGAAC[A/C]CCTTTCTTGAACATC | 5663 |
rs144459293 | in-del | -/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73218860 | ATCTTTTAATTTTTT[-/T]CAAAGTAGTTTTACT | 5663 |
rs144466165 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | PSEN1 | GRCh38.p7 | 14:73189896 | TGGTCTCCCTTGACC[A/G]GGTGGGCACTGAGCA | 5663 |
rs144467541 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PSEN1 | GRCh38.p7 | 14:73154122 | CCACGTAGGCATGTT[A/G]ACTGCTTACATGCGT | 5663 |
rs144522334 | in-del | -/ATC | 0.0517044 | 0.152246 | intron-variant | PSEN1 | GRCh38.p7 | 14:73188296 | TTGCCATATTACTAG[-/ATC]ATCATCTCTGTATGT | 5663 |
rs144572101 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PSEN1 | GRCh38.p7 | 14:73158298 | TCTATCTATCTATCT[A/G]TCTATCTATCTATCT | 5663 |
rs144669072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73155723 | GGGGTCTCGTTATGT[C/T]GCCCAGGCCGGTCTT | 5663 |
rs144677677 | snp | G/T | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73153546 | ATAAATGTTTTCAAG[G/T]TTTCCACTTAACTTG | 5663 |
rs144680586 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | PSEN1 | GRCh38.p7 | 14:73221805 | GCTAGTCTTCCACCA[C/T]GAAAAATAGATTGTC | 5663 |
rs144725513 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73220687 | CAGCTCCACAAATGG[A/G]TGCTTTGTGGTCTCT | 5663 |
rs144737303 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PSEN1 | GRCh38.p7 | 14:73199967 | GACCAGGCTGGTCTC[A/G]AACTCCTGACTTCAG | 5663 |
rs144777325 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | PSEN1 | GRCh38.p7 | 14:73144528 | TCATTGCTGTAAACT[A/C]CTACGGGGCAGGTTT | 5663 |
rs144829044 | snp | C/T | 0.00398367 | 0.0444518 | intron-variant | PSEN1 | GRCh38.p7 | 14:73208945 | GCCCCTCCTCAGTCT[C/T]CCTCCCATGCTTGTC | 5663 |
rs144940990 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73164532 | ATCCCAGTAGAATTT[A/G]CAACAACCCTATCAG | 5663 |
rs144980869 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73207812 | CCAGGCATGGAGCAG[C/T]GAGGAGTGCATGAGC | 5663 |
rs145022303 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | PSEN1 | GRCh38.p7 | 14:73220593 | AACCAACTGCCAAGG[A/G]GAAAGAGAAGGGGCC | 5663 |
rs145060922 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73205008 | TTTGATCATTTGGTT[A/G]GGTTATCCTATAATG | 5663 |
rs145082857 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSEN1 | GRCh38.p7 | 14:73138380 | TCCGCCACCACGCCC[A/G]GCTAATTTTTTTGTA | 5663 |
rs145088047 | snp | A/G | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73168536 | AATCAGGTGAGCGTT[A/G]GAGACTATGGATGGG | 5663 |
rs145101663 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | PSEN1 | GRCh38.p7 | 14:73152574 | ATTGTGCCACTGCAC[C/T]CCAGTGCAGTGTGAC | 5663 |
rs145148407 | snp | A/C/T | 0.0448899 | 0.143025 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73134615 | TCACTGCAACCTCTG[A/C/T]CTTCCAGGCTCAAGC | 5663 |
rs145154229 | snp | C/G | 0.0345262 | 0.126772 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204097 | TCCGCCTCCTGGATT[C/G]AAGCAATTCTCCTGC | 5663 |
rs145175423 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156262 | TTGGGAGGCTGAGGT[C/T]GGAGGATGACTTGAG | 5663 |
rs145214439 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | PSEN1 | GRCh38.p7 | 14:73156040 | GTGGATCTAAGTTTG[C/T]ATTTAAAAATATTTT | 5663 |
rs145353205 | in-del | -/GT | | | intron-variant | PSEN1 | GRCh38.p7 | 14:73191412 | AGTGTGTGTGTGTGT[-/GT]ATGATGATTCTTCTC | 5663 |
rs145370761 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PSEN1 | GRCh38.p7 | 14:73160664 | TTCTTTTTTCCCCCC[A/G]TATTACACAGATGTA | 5663 |
rs145406041 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73192180 | CCGTGGCTCATGCTT[A/G]TAATCCCAGCACTTT | 5663 |
rs145412152 | in-del | -/GAGAGG | 0.0517044 | 0.152246 | intron-variant | PSEN1 | GRCh38.p7 | 14:73185616 | GAGACCGTGGGGAGA[-/GAGAGG]GAGAGGGAGAGGGAG | 5663 |
rs145427499 | snp | C/T | 0.0260105 | 0.111035 | upstream-variant-2KB | PSEN1 | GRCh38.p7 | 14:73135487 | ATTCTCCTGCTGCAG[C/T]CTCCCGAGTAGCTGG | 5663 |
rs145441531 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSEN1 | GRCh38.p7 | 14:73142404 | AGTAGCTTAGAGACA[C/T]TAAAACAAGCCACAA | 5663 |
rs145472990 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187765 | TAATACTAAGTGTTC[C/T]GAACATATAAAAAGA | 5663 |
rs145496879 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73172735 | AATAATGCACATACT[G/T]TCTCTCTCATAGAGT | 5663 |
rs145510210 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PSEN1 | GRCh38.p7 | 14:73200724 | AGATTTTTTTTGCCA[A/G]TTTTTCTGTTGAGTT | 5663 |
rs145551368 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | PSEN1 | GRCh38.p7 | 14:73145880 | GGGAGGCTGAGGTGG[A/G]TGGATCACTTGTGGT | 5663 |
rs145575064 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PSEN1 | GRCh38.p7 | 14:73139490 | GGAGGTGAGGCAGGA[G/T]AATCGCTTGAACCCA | 5663 |
rs145583388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSEN1 | GRCh38.p7 | 14:73187117 | CTCCTTGCTTATAAT[A/G]AGTAGAACTGAAAGA | 5663 |
rs145607385 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | PSEN1 | GRCh38.p7 | 14:73204794 | GTAATCCTAGCACTT[C/T]GGGAGGCTGAGGCGG | 5663 |