SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs9626 | snp | C/T | 0.419305 | 0.183945 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011825 | CCCCGAGTTCCCGCC[C/T]GCCGCGGCACAGGTG | 138151 |
rs9753 | snp | C/T | 0.31352 | 0.241796 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011789 | GCAACGCATCTACGC[C/T]GAGCGGCGGGGCGAC | 138151 |
rs871093 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | NACC2 | GRCh38.p7 | 9:136063057 | TCACTGTTTTCTTCT[A/G]ATTTTTGTTCTCGTT | 138151 |
rs871094 | snp | C/T | 0.156319 | 0.231784 | intron-variant | NACC2 | GRCh38.p7 | 9:136062849 | CTAAGCCTGGGAGGC[C/T]GAGGCCGCAGTGTGC | 138151 |
rs871095 | snp | A/G | 0.432944 | 0.170387 | intron-variant | NACC2 | GRCh38.p7 | 9:136063400 | GCTTCTGCAATGTAC[A/G]TGACCTCTTTCCTGG | 138151 |
rs884558 | snp | A/G | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136047756 | GCTGCGGTCCTGCTG[A/G]CTCCCCAAAAACCCA | 138151 |
rs884559 | snp | C/T | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136047816 | CTCACGAAGTCCAGG[C/T]GATGTGAGGGCTTAA | 138151 |
rs939612 | snp | C/T | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136048701 | CCTGTGCAGCGTCTG[C/T]CACCACAGCCGGGAC | 138151 |
rs939613 | snp | G/T | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136048451 | GGTAGGGCTTGATTT[G/T]TCCTGAGACTGGGAG | 138151 |
rs1007411 | snp | C/T | 0.040671 | 0.13668 | intron-variant | NACC2 | GRCh38.p7 | 9:136043730 | CAGGGTAACATTCTA[C/T]AGGAGGGAACTGTTC | 138151 |
rs1107549 | snp | C/T | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136049174 | CTCGGCTCAGCACAC[C/T]GGGCGCTTCCTGGCC | 138151 |
rs1164962 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NACC2 | GRCh38.p7 | 9:136024184 | cacacacacacactc[C/T]gtcctcacacacaca | 138151 |
rs1183712 | snp | C/T | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136024454 | CTCTGTCCTCACACA[C/T]ACCCTCTGTCCTCAC | 138151 |
rs1335098 | snp | A/C | 0.251014 | 0.249998 | intron-variant | NACC2 | GRCh38.p7 | 9:136035262 | accacctggcagaga[A/C]cacctgcaccaaacc | 138151 |
rs1335099 | snp | C/T | 0.0926964 | 0.194308 | intron-variant | NACC2 | GRCh38.p7 | 9:136035337 | ACTCCTGTGACGCAC[C/T]GAGAAGGTTCCGCTG | 138151 |
rs1402643 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136028184 | TCTCTCTGTCACtca[A/G]gctggatgctcctgc | 138151 |
rs1464424 | snp | A/G | 0.375 | 0.216506 | intron-variant | NACC2 | GRCh38.p7 | 9:136046947 | TCCACCCTCTCTCGC[A/G]TTAAGAACCATGGAC | 138151 |
rs1464425 | snp | C/T | 0.375 | 0.216506 | intron-variant | NACC2 | GRCh38.p7 | 9:136046760 | CCTCCCTCCAGGTCC[C/T]GCGTCACCACCCGTC | 138151 |
rs1521444 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136043727 | CCCCAGGGTAACATT[C/G]TACAGGAGGGAACTG | 138151 |
rs1572290 | snp | A/G | 0.417359 | 0.185718 | intron-variant | NACC2 | GRCh38.p7 | 9:136032006 | GGGGTGCTGCCGAGG[A/G]CGACCCTTGCCCCCC | 138151 |
rs1572291 | snp | A/C | 0.173965 | 0.238157 | intron-variant | NACC2 | GRCh38.p7 | 9:136032003 | GTGCTGCCGAGGACG[A/C]CCCTTGCCCCCCATT | 138151 |
rs1615391 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | NACC2 | GRCh38.p7 | 9:136090916 | CACTTTCAGGCCCCT[C/T]TGTTCCCCGCCCCCA | 138151 |
rs1717416 | snp | C/T | 0.499154 | 0.0205497 | intron-variant | NACC2 | GRCh38.p7 | 9:136090835 | TCCCAAGCCCAGGGC[C/T]GGCCGGCCCCAGCTC | 138151 |
rs1717417 | snp | A/G | 0.0995161 | 0.199636 | intron-variant | NACC2 | GRCh38.p7 | 9:136090548 | TGGGTGCCTGCTGAG[A/G]GAAGACTTGCTAGCA | 138151 |
rs1717418 | snp | A/C | 0.489376 | 0.0721049 | intron-variant | NACC2 | GRCh38.p7 | 9:136090247 | GGACCCCTGAGGCAT[A/C]CCCTCTGGCCAGGGC | 138151 |
rs1717451 | snp | A/G | 0.304688 | 0.243945 | intron-variant | NACC2 | GRCh38.p7 | 9:136093846 | CCTAGAGTTAGGTCA[A/G]GGTTCAGGCAGCCCC | 138151 |
rs1717452 | snp | C/T | 0.305436 | 0.243776 | intron-variant | NACC2 | GRCh38.p7 | 9:136093715 | AAAGAGGCCTCTTGG[C/T]GTTTTCCCCTGGGGT | 138151 |
rs1717453 | snp | A/G | 0.304937 | 0.243889 | intron-variant | NACC2 | GRCh38.p7 | 9:136093588 | TGGAATGGGCACAGA[A/G]AGTGGAACAAGATAT | 138151 |
rs1717454 | snp | G/T | 0.305186 | 0.243833 | intron-variant | NACC2 | GRCh38.p7 | 9:136093381 | GGCTGCTGGAAGGGT[G/T]CGCAGGGCTGCTCTG | 138151 |
rs1717455 | snp | C/T | 0.305186 | 0.243833 | intron-variant | NACC2 | GRCh38.p7 | 9:136093295 | TTTCCAATTAAAGCA[C/T]GAGGCTGCATTATTC | 138151 |
rs1717456 | snp | A/G | 0.305186 | 0.243833 | intron-variant | NACC2 | GRCh38.p7 | 9:136093230 | TTCTTCCAGGCCTGC[A/G]CTCCTCTTGGCCTCT | 138151 |
rs1717457 | snp | C/T | 0.304937 | 0.243889 | intron-variant | NACC2 | GRCh38.p7 | 9:136093127 | AAGGTGTTGTCCTTT[C/T]CGGGATGTTGAGTTC | 138151 |
rs1996743 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136052929 | CCTGGGCTCATACCA[C/G]CCTCTCTGCGTGGGG | 138151 |
rs2139881 | snp | C/T | 0.301681 | 0.2446 | intron-variant | NACC2 | GRCh38.p7 | 9:136021694 | ATGCCCCAGGCTAGA[C/T]GCAGCCCGGATGTCC | 138151 |
rs2139882 | snp | A/G | 0.284209 | 0.247648 | intron-variant | NACC2 | GRCh38.p7 | 9:136029992 | ACAGAGGTTTCTGGC[A/G]GGTGAAGCGACACCC | 138151 |
rs2275107 | snp | A/G | 0.248847 | 0.250004 | synonymous-codon, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016404 | GCCTGAGCCAGTGCC[A/G]CTGGAGAGCCGCTCC | 138151 |
rs2275108 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015933 | AGTTGCAGCCTTTGA[C/G]GGTAACGGCCAGGTT | 138151 |
rs2280484 | snp | C/G | 0.241053 | 0.24984 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012994 | ATCACACTTGGAAAC[C/G]TACCAAGAACGTTAA | 138151 |
rs2280485 | snp | C/T | 0.494624 | 0.051568 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013151 | CCTCAGGCTGGGATC[C/T]GAACCCAGCCCCGGC | 138151 |
rs2280486 | snp | C/T | 0.491337 | 0.0652412 | synonymous-codon, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013290 | GCAGCTGTTGGCCAG[C/T]GTGTTCCTGGTGGAG | 138151 |
rs2280487 | snp | C/G | 0.40263 | 0.198 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013368 | GGCGACCCGCCCGCA[C/G]GAATGCCCTGCTGGG | 138151 |
rs2385188 | snp | C/T | 0.472522 | 0.113946 | intron-variant | NACC2 | GRCh38.p7 | 9:136063355 | GAGGGGCTCGAGTCC[C/T]GTGCCTATTGGTCAT | 138151 |
rs3004014 | snp | C/T | 0.0685596 | 0.171987 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096229 | TCGGGACCACTGAGG[C/T]GGTATCACTCCATTC | 138151 |
rs3811129 | snp | C/T | 0.221737 | 0.248397 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009832 | CCCCTCCGGTGTGCA[C/T]ACAGGCCAGTGAGCG | 138151 |
rs3811130 | snp | A/G | 0.331179 | 0.236453 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009810 | CAGTGAGCGGTGGCC[A/G]ACCAGCGCACCCCAC | 138151 |
rs3811131 | snp | G/T | 0.331411 | 0.236373 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009737 | TAGGGGAGGACCATG[G/T]GCTGCACCCTGGCCT | 138151 |
rs3841030 | in-del | -/C | 0.471768 | 0.115407 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009844 | GCCCATCAGCACCCC[-/C]TCCGGTGTGCACACA | 138151 |
rs3922922 | snp | A/G | 0.360421 | 0.224293 | intron-variant | NACC2 | GRCh38.p7 | 9:136074866 | TCGGCTGGGAAGGCC[A/G]CGCTTCCTGCCGCTC | 138151 |
rs4384058 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | NACC2 | GRCh38.p7 | 9:136075305 | AGAGCTGGCTGCGGC[C/T]GCCTGGCTGGGATAC | 138151 |
rs4409473 | snp | C/T | 0.462034 | 0.132445 | intron-variant | NACC2 | GRCh38.p7 | 9:136031934 | CACAGCTGATGTGTA[C/T]GGGCAGCTGTTAACA | 138151 |
rs4419885 | snp | C/G | 0.493477 | 0.0567349 | intron-variant | NACC2 | GRCh38.p7 | 9:136074588 | ATTAACACAGACGGA[C/G]AGGTCAAAACCATTC | 138151 |
rs4454361 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136052544 | CAGGCAGTGGGTGGG[C/T]GAGGCGGCACCCCAG | 138151 |
rs4500151 | snp | C/G | 0.277778 | 0.248452 | intron-variant | NACC2 | GRCh38.p7 | 9:136047135 | AGAGACAGCTACCTG[C/G]CTCCACTCCTGCACG | 138151 |
rs4562408 | snp | A/G | 0.236724 | 0.249647 | intron-variant | NACC2 | GRCh38.p7 | 9:136075365 | GAGGCTGGCTGCTGC[A/G]AACTGACTGAAGCGC | 138151 |
rs4601410 | snp | A/G | 0.237882 | 0.249706 | intron-variant | NACC2 | GRCh38.p7 | 9:136075422 | GGCTTGGAACTCGGA[A/G]GCGAATGTCTCCCCG | 138151 |
rs4841905 | snp | C/T | 0.361053 | 0.22398 | intron-variant | NACC2 | GRCh38.p7 | 9:136020203 | GAACAAATGAACGAA[C/T]GTCAGAAGGAGGGGG | 138151 |
rs4841906 | snp | A/G | 0.434543 | 0.168653 | intron-variant | NACC2 | GRCh38.p7 | 9:136023175 | CTCTGGGTCTCCTGG[A/G]AACCCGGATGGAAAG | 138151 |
rs4841907 | snp | A/G | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136046087 | GGGGCTCCCGCTCAG[A/G]CCACAGCACCACCAA | 138151 |
rs4841908 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136053757 | CTTCGCCCCAAGGAC[A/G]GGGGGGTAGGGATGT | 138151 |
rs4841909 | snp | A/G | 0.394538 | 0.203982 | intron-variant | NACC2 | GRCh38.p7 | 9:136064874 | GACAGACTTAGATCA[A/G]TGGAACAGATGAGTC | 138151 |
rs4841910 | snp | A/G | 0.413083 | 0.189483 | intron-variant | NACC2 | GRCh38.p7 | 9:136076100 | ACAGGCACCCTTCGC[A/G]GCCTCTGCCTGATTT | 138151 |
rs4841911 | snp | C/T | 0.41325 | 0.18934 | intron-variant | NACC2 | GRCh38.p7 | 9:136076137 | CAGTAGTGATGACAC[C/T]CCATACCCCGTGACA | 138151 |
rs4841912 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | NACC2 | GRCh38.p7 | 9:136077048 | agccgggtgtggtgg[C/T]gggcgcctgtagtcc | 138151 |
rs4841913 | snp | C/G/T | 0.117188 | 0.211804 | intron-variant | NACC2 | GRCh38.p7 | 9:136077050 | ccgggtgtggtggcg[C/G/T]gcgcctgtagtccca | 138151 |
rs4841914 | snp | C/G | 0.0807149 | 0.183963 | intron-variant | NACC2 | GRCh38.p7 | 9:136077063 | cgggcgcctgtagtc[C/G]cagccacttgggagg | 138151 |
rs4841915 | snp | C/T | 0.393065 | 0.205018 | intron-variant | NACC2 | GRCh38.p7 | 9:136077067 | cgcctgtagtcccag[C/T]cacttgggaggctga | 138151 |
rs4841916 | snp | C/G | 0.316726 | 0.240931 | intron-variant | NACC2 | GRCh38.p7 | 9:136077545 | CAAAGGGCGTGTGGT[C/G]AGAGTATGGAAAGAA | 138151 |
rs4842070 | snp | C/G | 0.0879971 | 0.190408 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007047 | CAGTGCCATCCAAAT[C/G]TTCAAGTCAAAAATA | 138151 |
rs4842071 | snp | A/G | 0.26326 | 0.249648 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010451 | ACTAGTCGCCCACCC[A/G]GGACCCCCTTTTTCC | 138151 |
rs4842072 | snp | A/G | 0.221439 | 0.248363 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010746 | CACGTCCCACAGTGG[A/G]CCCGGGCGGGACAGT | 138151 |
rs4842073 | snp | A/C | 0.499996 | 0.00139776 | intron-variant | NACC2 | GRCh38.p7 | 9:136021468 | acccccaagtgctgg[A/C]gaggacacggggcag | 138151 |
rs4842074 | snp | A/G | 0.376791 | 0.215463 | intron-variant | NACC2 | GRCh38.p7 | 9:136021558 | gcttggtggcttctt[A/G]tcaagttcaacatac | 138151 |
rs4842075 | snp | C/T | 0.364609 | 0.222182 | intron-variant | NACC2 | GRCh38.p7 | 9:136021837 | CTGTTACACAGAAGA[C/T]GTAAAATGATTACAT | 138151 |
rs4842076 | snp | C/T | 0.495963 | 0.0447464 | intron-variant | NACC2 | GRCh38.p7 | 9:136021943 | CCAGGGGCTGGGGTG[C/T]GGACAAGCCTCAAGG | 138151 |
rs4842077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136022757 | CAGAAAGACCAGAAA[C/T]GACTTCCACGCTGTA | 138151 |
rs4842078 | snp | C/G | 0.284209 | 0.247648 | intron-variant | NACC2 | GRCh38.p7 | 9:136028032 | tgggaggccaaggtg[C/G]gtggatcacttgagg | 138151 |
rs4842079 | snp | G/T | 0.498589 | 0.02652 | intron-variant | NACC2 | GRCh38.p7 | 9:136031992 | CTGCATAAATGAATG[G/T]GGGGCAAGGGTCGTC | 138151 |
rs4842080 | snp | A/T | 0.464309 | 0.12873 | intron-variant | NACC2 | GRCh38.p7 | 9:136032177 | AAAGGAGGGGAAGGA[A/T]TATCAGCGAGCTGCA | 138151 |
rs4842081 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136033940 | GTGTGTGTGTGTGTG[A/T]GAGATATTTGGCAAT | 138151 |
rs4842083 | snp | A/G | 0.375 | 0.216506 | intron-variant | NACC2 | GRCh38.p7 | 9:136036983 | agataaaagcagcct[A/G]agaagaagacacaat | 138151 |
rs4842084 | snp | A/G | 0.375399 | 0.216275 | intron-variant | NACC2 | GRCh38.p7 | 9:136043624 | GGTCTCACGCACAGG[A/G]ATCCTATGAGAAGCA | 138151 |
rs4842085 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136045333 | TGTGGCCAGAGCTGT[C/T]CCCTGCCAGGAAAGG | 138151 |
rs4842086 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136045340 | AGAGCTGTCCCCTGC[C/T]AGGAAAGGGTTACCG | 138151 |
rs4842087 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136045341 | GAGCTGTCCCCTGCC[A/G]GGAAAGGGTTACCGT | 138151 |
rs4842088 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136045353 | GCCAGGAAAGGGTTA[C/T]CGTCACGGGCCCACG | 138151 |
rs4842089 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136045417 | AGGGTTACCGTGGAA[A/G]TGTGCAGCTGGTGTC | 138151 |
rs4842090 | snp | A/C | 0.489796 | 0.070696 | intron-variant | NACC2 | GRCh38.p7 | 9:136049080 | TCTCCAATTAGGGCA[A/C]CCTGGGTTTGTGGGG | 138151 |
rs4842091 | snp | A/G | 0.378372 | 0.214524 | intron-variant | NACC2 | GRCh38.p7 | 9:136055321 | AAGGACACAGGTTAC[A/G]AGGTTGGTGCCAGGC | 138151 |
rs4842092 | snp | A/G | 0.481932 | 0.0933148 | intron-variant | NACC2 | GRCh38.p7 | 9:136055860 | GTGAGGACATCTCCT[A/G]AAAGGTCAATCGAAG | 138151 |
rs4842093 | snp | A/T | 0.427727 | 0.175821 | intron-variant | NACC2 | GRCh38.p7 | 9:136055985 | AGTCTGGGGGCTGCT[A/T]CCCCGTGGACCTTGC | 138151 |
rs4842095 | snp | C/G | 0.29278 | 0.246313 | intron-variant | NACC2 | GRCh38.p7 | 9:136057028 | CCCAGCCCCCACCCC[C/G]AGGGTGGGCCTCCAG | 138151 |
rs4842096 | snp | A/G | 0.294832 | 0.245947 | intron-variant | NACC2 | GRCh38.p7 | 9:136064784 | TTAAAAAAGAGGAGC[A/G]AAGTTAGAGCAGTCA | 138151 |
rs4842097 | snp | A/G | 0.41023 | 0.191902 | intron-variant | NACC2 | GRCh38.p7 | 9:136067844 | tctcaaaaacacaga[A/G]acaaaaccaaagcca | 138151 |
rs4842098 | snp | A/T | 0.231111 | 0.249285 | intron-variant | NACC2 | GRCh38.p7 | 9:136072256 | aaagaaaaaaaaaaa[A/T]acccaaaggcagggc | 138151 |
rs4842099 | snp | C/T | 0.21875 | 0.248039 | intron-variant | NACC2 | GRCh38.p7 | 9:136075689 | GCTCCCTGTGCCCGG[C/T]CTTCCACACGCGGGG | 138151 |
rs4842100 | snp | A/G | 0.155325 | 0.23138 | intron-variant | NACC2 | GRCh38.p7 | 9:136076140 | TAGTGATGACACCCC[A/G]TACCCCGTGACATCC | 138151 |
rs4842101 | snp | A/G | 0.41325 | 0.18934 | intron-variant | NACC2 | GRCh38.p7 | 9:136076182 | TATGCAACCAAAAGA[A/G]AAGCAAATGATTTCC | 138151 |
rs4842102 | snp | C/T | 0.396 | 0.202938 | intron-variant | NACC2 | GRCh38.p7 | 9:136076351 | GAGCCAGGTTTCCTG[C/T]CCATACCACGACAAA | 138151 |
rs4842103 | snp | C/T | 0.481319 | 0.0948228 | intron-variant | NACC2 | GRCh38.p7 | 9:136076541 | CAGGGGCTGGGGGAC[C/T]GCGGAGGGGAGTTGG | 138151 |
rs4842104 | snp | C/T | 0.404559 | 0.196498 | intron-variant | NACC2 | GRCh38.p7 | 9:136076697 | GAATTTCATGTTGTG[C/T]ATATTTGACTACAAT | 138151 |
rs4842105 | snp | A/G | 0.38555 | 0.210062 | intron-variant | NACC2 | GRCh38.p7 | 9:136076940 | gaacccaggaggcag[A/G]gcctgcagtgagccg | 138151 |
rs4842106 | snp | G/T | 0.408871 | 0.193029 | intron-variant | NACC2 | GRCh38.p7 | 9:136076985 | CACTCCAGCCTGGGC[G/T]ACAGAGCGAGACTCT | 138151 |
rs4842107 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | NACC2 | GRCh38.p7 | 9:136077518 | AGACCTTTGCAACAT[A/G]TGTATCTTCAGCAAA | 138151 |
rs4842108 | snp | C/T | 0.416708 | 0.186302 | intron-variant | NACC2 | GRCh38.p7 | 9:136080258 | TCCCAGCAGGGCCCC[C/T]GCACCCATCTCTGTG | 138151 |
rs4842109 | snp | A/G | 0.0988009 | 0.199095 | intron-variant | NACC2 | GRCh38.p7 | 9:136088556 | CACTTGGGGCTCGTG[A/G]GGACCCAGGTCCGGT | 138151 |
rs4842110 | snp | A/G | 0.214541 | 0.247473 | intron-variant | NACC2 | GRCh38.p7 | 9:136088640 | AACCACGATGGCCTC[A/G]TTGAGGCCCCCACCC | 138151 |
rs5019677 | snp | A/G | 0.289424 | 0.246872 | intron-variant | NACC2 | GRCh38.p7 | 9:136030479 | gccaggcatggtggc[A/G]ggcgcctgtagtccc | 138151 |
rs5901094 | in-del | -/A | 0.290718 | 0.246662 | intron-variant | NACC2 | GRCh38.p7 | 9:136030610 | GCAAGACTCCGTCTC[-/A]AAAAAAAAATAAAAA | 138151 |
rs5901095 | in-del | -/A | 0.409721 | 0.192325 | intron-variant | NACC2 | GRCh38.p7 | 9:136073654 | CAAGAATGTTTGCAG[-/A]AAAGTCGACTTGATT | 138151 |
rs6537926 | snp | A/G | 0.283947 | 0.247685 | intron-variant | NACC2 | GRCh38.p7 | 9:136030338 | CTGGAggccgggcgc[A/G]gtggctcacgcctgt | 138151 |
rs7018676 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | NACC2 | GRCh38.p7 | 9:136090793 | CCCCCAGCCCAGGGC[C/T]GGGCTGCCCTCGGGG | 138151 |
rs7019243 | snp | C/T | 0.459914 | 0.13578 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096722 | GTTCTGAGTGCCTCC[C/T]ACACCCAGGGCATGA | 138151 |
rs7023817 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136055115 | AGGCTGAGATCCAGG[C/T]CTGCCCTGCCCTGGG | 138151 |
rs7024676 | snp | A/G | 0.397813 | 0.201621 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010944 | TGCACACACACGCAC[A/G]CACACACACTCGTGC | 138151 |
rs7024715 | snp | C/T | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136033598 | gaggttggagtgagc[C/T]gagatctgccactgc | 138151 |
rs7025705 | snp | C/T | 0.00639321 | 0.0561759 | synonymous-codon, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013230 | GACCCGGCTGTCCAG[C/T]GGCTTCCGGCTGGGG | 138151 |
rs7025716 | snp | C/T | 0.43655 | 0.16643 | intron-variant | NACC2 | GRCh38.p7 | 9:136043330 | AAAAGTTATAAAGTA[C/T]GGCTTATTCAACCTG | 138151 |
rs7026190 | snp | G/T | 0.49706 | 0.0382258 | intron-variant | NACC2 | GRCh38.p7 | 9:136068583 | ATTTTTCAGCTCTAT[G/T]ATAATCTCATGAGAG | 138151 |
rs7027118 | snp | C/T | 0.497091 | 0.0380279 | intron-variant | NACC2 | GRCh38.p7 | 9:136068551 | TTATGATGGCTACAT[C/T]GTCACTAGGCAATAG | 138151 |
rs7028313 | snp | C/T | 0.499776 | 0.0105807 | intron-variant | NACC2 | GRCh38.p7 | 9:136071388 | TCTCTACTAAAGATA[C/T]GAAAATTAGTTGAGC | 138151 |
rs7028545 | snp | C/T | 0.487368 | 0.0784625 | intron-variant | NACC2 | GRCh38.p7 | 9:136071524 | CTCCAGCCTGGATGA[C/T]AGAGTGAGACTCCAT | 138151 |
rs7029290 | snp | A/G | 0.405255 | 0.195948 | intron-variant | NACC2 | GRCh38.p7 | 9:136065017 | CATGCAAAAGAATGA[A/G]GCAGGACCCTTCCCT | 138151 |
rs7029928 | snp | G/T | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136059356 | CGGAGCAGGGCCCTA[G/T]GACATGCCAGCTCAG | 138151 |
rs7032673 | snp | A/T | 0.394538 | 0.203982 | intron-variant | NACC2 | GRCh38.p7 | 9:136065063 | AATTAACTTAAAATA[A/T]TTCAAAGACCTAAAT | 138151 |
rs7033408 | snp | A/G | | | intron-variant, upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136052451 | CCAGGGGGAGGGGGT[A/G]AGGGGGTCAGGACAG | 138151 |
rs7034427 | snp | C/T | 0.379158 | 0.214052 | intron-variant | NACC2 | GRCh38.p7 | 9:136083284 | TGCTTCACCCCAACC[C/T]GAGCCTAGGCACGCG | 138151 |
rs7034930 | snp | A/G | 0.293807 | 0.246132 | intron-variant | NACC2 | GRCh38.p7 | 9:136063191 | TCCCATTACGTGGCG[A/G]GGACCAGGGATGAGC | 138151 |
rs7035807 | snp | A/G | 0.0872718 | 0.189788 | intron-variant | NACC2 | GRCh38.p7 | 9:136087993 | CTGCTGGGAAGTTCC[A/G]GGAGGTGACCTGGGG | 138151 |
rs7035831 | snp | A/G | 0.498034 | 0.0312882 | intron-variant | NACC2 | GRCh38.p7 | 9:136088045 | GGTGACCTGGAAGAC[A/G]GGCACCCCCAGTGGC | 138151 |
rs7035843 | snp | A/G | 0.0858192 | 0.188533 | intron-variant | NACC2 | GRCh38.p7 | 9:136088076 | TGTCATCTCATGCAC[A/G]GAGGTCAGCAGTATT | 138151 |
rs7035997 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | NACC2 | GRCh38.p7 | 9:136084675 | gacagccaagaggca[A/G]gtggccccagggtcc | 138151 |
rs7036100 | snp | A/C | 0.380919 | 0.21298 | intron-variant | NACC2 | GRCh38.p7 | 9:136033364 | AAAATGAACTTCTGG[A/C]CGGGCACGGTGGCTC | 138151 |
rs7036473 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136079044 | TGTTAATTTGACTTC[A/G]ATCATAGCTTCTTCT | 138151 |
rs7037215 | snp | C/G | 0.030278 | 0.119257 | intron-variant | NACC2 | GRCh38.p7 | 9:136088440 | TCCCAGCAGCTGCCC[C/G]TGAGCCCCTGGAAGC | 138151 |
rs7037873 | snp | A/C | 0.497613 | 0.0344622 | intron-variant | NACC2 | GRCh38.p7 | 9:136075755 | GACCCACCCAACACC[A/C]ACAGGCCCTGTCGGT | 138151 |
rs7039648 | snp | C/T | 0.490119 | 0.0695896 | intron-variant | NACC2 | GRCh38.p7 | 9:136071173 | GGGAGGCAGACGTTG[C/T]GGTGAGCCAAGATCA | 138151 |
rs7040209 | snp | A/G | 0.5 | 0.000399361 | intron-variant | NACC2 | GRCh38.p7 | 9:136028950 | tggatgttgggcacc[A/G]tcgagcacaagaggg | 138151 |
rs7040738 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | NACC2 | GRCh38.p7 | 9:136029377 | cttgagagctgtact[A/G]tccctcaataaagca | 138151 |
rs7041423 | snp | A/G | 0.489259 | 0.0724914 | intron-variant | NACC2 | GRCh38.p7 | 9:136080565 | CAACAGCGAAACTCC[A/G]TCTCCCCACTACCCT | 138151 |
rs7041980 | snp | C/T | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136037428 | ACCAcagTTTGCATA[C/T]TCATTACTAATTACT | 138151 |
rs7042368 | snp | A/T | 0.498437 | 0.0279115 | intron-variant | NACC2 | GRCh38.p7 | 9:136068031 | ATAGGATAAAAGATT[A/T]AAAATGGTACAACTC | 138151 |
rs7043846 | snp | C/T | 0.0259836 | 0.11098 | missense | NACC2 | GRCh38.p7 | 9:136011824 | ACACCTGTGCCGCGG[C/T]AGGCGGGAACTCGGG | 138151 |
rs7044271 | snp | C/T | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136035011 | AGGCAGGAGAATCAC[C/T]TGAACCCAGGAGGCA | 138151 |
rs7044622 | snp | A/C | 0.0678174 | 0.1712 | intron-variant | NACC2 | GRCh38.p7 | 9:136093037 | GGGCCACTGGGCACT[A/C]GGTGCCCTGTGCGTT | 138151 |
rs7044661 | snp | A/T | 0.0744748 | 0.178019 | intron-variant | NACC2 | GRCh38.p7 | 9:136080588 | ACTACCCTGCTCCAA[A/T]AAAAAAACTCCAACG | 138151 |
rs7044770 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136080811 | ATGCAGGGAGAGCAG[A/T]CGGCAGATGACCACA | 138151 |
rs7046402 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136053526 | CTCCACCCTCAGGTC[C/T]CCACTTAGTTTCTGC | 138151 |
rs7048213 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136094160 | GGAACGCGCAGCAGA[C/G]AACACAGCTCAGGGC | 138151 |
rs7048852 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136053692 | TCACAGACCCACTGC[A/G]CCCACCACCAGGAGC | 138151 |
rs7388909 | snp | C/T | 0.399611 | 0.200291 | intron-variant | NACC2 | GRCh38.p7 | 9:136027362 | CTGAGGTGGCTCTGC[C/T]GTGGCCAACACAAGA | 138151 |
rs7468351 | snp | C/T | 0.499933 | 0.00579035 | intron-variant | NACC2 | GRCh38.p7 | 9:136083043 | ATGAAAGCGACCAGA[C/T]TGATCTCCTGACGAC | 138151 |
rs7468849 | snp | C/T | 0.49949 | 0.0159663 | intron-variant | NACC2 | GRCh38.p7 | 9:136088270 | CTGTACCACTGCCCA[C/T]ATCAGGCCCAGATGG | 138151 |
rs7470255 | snp | C/T | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136073502 | CAGGGGGTGTGAGCG[C/T]GGATCCAGCTGTATC | 138151 |
rs7847679 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136048824 | CCCATCAGGGCACAG[G/T]GATATGCGTGGTGGG | 138151 |
rs7847985 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136045494 | CTGCCAGCTGCAATT[A/T]AACATCTGCCCGCCC | 138151 |
rs7848231 | snp | C/T | 0.259951 | 0.249802 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009473 | GTGGGCCCTGAGGAA[C/T]GGGTGGAGGGGCCGA | 138151 |
rs7848991 | snp | A/C | 0.495891 | 0.0451408 | intron-variant | NACC2 | GRCh38.p7 | 9:136070477 | gcgccactgcactcc[A/C]gcctgggcgacagag | 138151 |
rs7849117 | snp | C/T | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136049258 | ACTCTCTAGACCTGG[C/T]CGGGTGAGGCGCAGA | 138151 |
rs7851532 | snp | C/T | 0.118584 | 0.212673 | intron-variant | NACC2 | GRCh38.p7 | 9:136062107 | CTCCAGCCTGGGCAA[C/T]AGAGCGAGACAGGAC | 138151 |
rs7851993 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | NACC2 | GRCh38.p7 | 9:136032393 | cgaggaaaaaaaaaa[A/C]cctcttaacctagga | 138151 |
rs7852302 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | NACC2 | GRCh38.p7 | 9:136080353 | CAAAACCCAACCCAG[C/G]TTCTAGGAAAATCCG | 138151 |
rs7852562 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | NACC2 | GRCh38.p7 | 9:136079819 | GGCCACCAGGACAGG[C/G]AGCAGCCGGGGAAGT | 138151 |
rs7853694 | snp | A/G | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136095861 | ACGGGAGCGCCCTTG[A/G]GCGAACGTCTGCGGG | 138151 |
rs7857221 | snp | C/T | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136021064 | agaatgaaaaacttc[C/T]gatctctgaatgaag | 138151 |
rs7859516 | snp | A/T | 0.107694 | 0.205546 | intron-variant | NACC2 | GRCh38.p7 | 9:136077971 | tagagacggggtttc[A/T]ccatgttagccaggc | 138151 |
rs7859644 | snp | A/G | 0.225005 | 0.248747 | intron-variant | NACC2 | GRCh38.p7 | 9:136078052 | GCTGGGATTATAGGC[A/G]TGAGCCACCGCGTCC | 138151 |
rs7860379 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | NACC2 | GRCh38.p7 | 9:136027190 | agatagcgccactgc[A/C]ctccagcctggacga | 138151 |
rs7860750 | snp | C/T | 0.103794 | 0.20279 | intron-variant | NACC2 | GRCh38.p7 | 9:136081744 | CTGGGGCACCATCCC[C/T]ACCAAGTGGCGGCAG | 138151 |
rs7861922 | snp | C/T | 0.499999 | 0.000599041 | intron-variant | NACC2 | GRCh38.p7 | 9:136030419 | tcgagaccatcccgg[C/T]gaacacagtgaaacc | 138151 |
rs7861958 | snp | C/T | 0.279991 | 0.248195 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015322 | GGCAGCCCAGCACTG[C/T]GCTCGCCATCCAGAA | 138151 |
rs7862055 | snp | A/G | 0.375 | 0.216506 | intron-variant | NACC2 | GRCh38.p7 | 9:136030731 | cagtggtgtcatctc[A/G]gctcactacaacctg | 138151 |
rs7862443 | snp | C/T | 0.25801 | 0.249872 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009754 | ATGGTCCTCCCCTAG[C/T]GGAGGCGGCCTCCGC | 138151 |
rs7862513 | snp | A/G | 0.207253 | 0.246318 | intron-variant | NACC2 | GRCh38.p7 | 9:136084068 | GAAGAGCGGGGAGGT[A/G]GGGAAGGTGGTGCTC | 138151 |
rs7864518 | snp | A/G | 0.375 | 0.216506 | intron-variant | NACC2 | GRCh38.p7 | 9:136049571 | GTGGCCTCCTGAGCC[A/G]CCCGGGTCCCAGGCA | 138151 |
rs7866192 | snp | A/C | 0.138886 | 0.22395 | intron-variant | NACC2 | GRCh38.p7 | 9:136061859 | GCGCGGTGGCTCACA[A/C]CTGTAATCCCAGCAC | 138151 |
rs7868482 | snp | C/T | 0.030278 | 0.119257 | intron-variant | NACC2 | GRCh38.p7 | 9:136089388 | GAAACCTAGCACCCG[C/T]GAAGGCCTGACTTCC | 138151 |
rs7868493 | snp | A/G | 0.0898077 | 0.191933 | intron-variant | NACC2 | GRCh38.p7 | 9:136076867 | CAAAAAAAATTAGCC[A/G]GGCGTGGTGGCGGGC | 138151 |
rs7869604 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | NACC2 | GRCh38.p7 | 9:136077003 | agagcgagactctgt[C/T]tcaaaaataaataaa | 138151 |
rs7872620 | snp | C/G | 0.5 | 0.00019968 | intron-variant | NACC2 | GRCh38.p7 | 9:136030061 | CGTAATTTTAGTAGA[C/G]ATGGAGTTTCACCAT | 138151 |
rs7873344 | snp | C/T | 0.0497397 | 0.151144 | intron-variant | NACC2 | GRCh38.p7 | 9:136083558 | caggtccagaggtgt[C/T]ttctgagaagggaaa | 138151 |
rs7874868 | snp | A/G | 0.198014 | 0.244535 | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006157 | TTGGGTGGCAGGTGA[A/G]GCAGATGAAGGGGCT | 138151 |
rs7875893 | snp | C/T | 0.201418 | 0.245234 | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006217 | TCCCGAAAAGGAGAC[C/T]CCCCGACCCTGGCAG | 138151 |
rs7876016 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | NACC2 | GRCh38.p7 | 9:136091365 | CAGCCTGGGCTGGGC[A/G]TTCTCCCAGGAGACC | 138151 |
rs9792601 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NACC2 | GRCh38.p7 | 9:136069158 | tgatctgcccgcctc[A/G]gcctcccaaagtgct | 138151 |
rs10114701 | snp | C/T | 0.280785 | 0.248097 | intron-variant | NACC2 | GRCh38.p7 | 9:136067443 | CGTGTTGATTAACGA[C/T]GGGGATATATCCTGA | 138151 |
rs10114772 | snp | A/G | 0.0861826 | 0.188849 | intron-variant | NACC2 | GRCh38.p7 | 9:136025167 | CCTGGAAGGGCTACA[A/G]GCTACGGTGTGAGGC | 138151 |
rs10115368 | snp | C/G | 0.497387 | 0.0360476 | intron-variant | NACC2 | GRCh38.p7 | 9:136067802 | ATCGCGGCACTGCCT[C/G]CAGTCTGGCAACAGG | 138151 |
rs10115486 | snp | A/G | 0.499477 | 0.0161657 | intron-variant | NACC2 | GRCh38.p7 | 9:136089587 | GCCCTCCCTCCTCTG[A/G]GGCTCCCCCAACTCA | 138151 |
rs10116108 | snp | A/G | 0.421368 | 0.182025 | intron-variant | NACC2 | GRCh38.p7 | 9:136035550 | aatgtgtgattctgg[A/G]ttaaataccacatca | 138151 |
rs10116614 | snp | C/T | 0.375 | 0.216506 | intron-variant | NACC2 | GRCh38.p7 | 9:136034851 | GTAACCCCAGCATTT[C/T]GGAAGGCACTGGCGG | 138151 |
rs10117001 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136045389 | TGTGGCCAGAGCTGT[C/T]CCCTGCTGGGAAAGG | 138151 |
rs10117908 | snp | C/G | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136046595 | GGGCCTGCCTCGCTG[C/G]GGGTGGGGGGGCTTG | 138151 |
rs10118673 | snp | A/C | 0.165853 | 0.235413 | intron-variant | NACC2 | GRCh38.p7 | 9:136047084 | GAGGAGCTCAGCCTG[A/C]AGGGACCTTAGAACA | 138151 |
rs10119505 | snp | A/T | 0.444666 | 0.15686 | intron-variant | NACC2 | GRCh38.p7 | 9:136069387 | aaccccttctctact[A/T]aaaatacaaaaatta | 138151 |
rs10122351 | snp | A/G | 0.496905 | 0.0392151 | intron-variant | NACC2 | GRCh38.p7 | 9:136069406 | ATACAAAAATTAGCC[A/G]GGCGTGGTGGCAGGC | 138151 |
rs10122618 | snp | C/T | 0.487368 | 0.0784625 | intron-variant | NACC2 | GRCh38.p7 | 9:136071730 | gtgatcaagactgtg[C/T]ggtatggacagaggg | 138151 |
rs10122801 | snp | A/C | 0.499767 | 0.0107802 | intron-variant | NACC2 | GRCh38.p7 | 9:136087343 | TGGATACCCTGCCCC[A/C]CTCCAACACACCCCA | 138151 |
rs10122974 | snp | A/G | 0.209084 | 0.246629 | intron-variant | NACC2 | GRCh38.p7 | 9:136045368 | CCGTCACGGGCCCAC[A/G]GGCCCTGTGGCCAGA | 138151 |
rs10125064 | snp | A/C | 0.499999 | 0.000599041 | intron-variant | NACC2 | GRCh38.p7 | 9:136026104 | cagcactttgggagg[A/C]cgaggtgggcagatc | 138151 |
rs10125541 | snp | A/G | 0.370974 | 0.218781 | intron-variant | NACC2 | GRCh38.p7 | 9:136018263 | GCTGAGCCTCGGGGC[A/G]TGGGGGGGCTGCCAA | 138151 |
rs10481726 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136043688 | CGTGGGGCCAGGATG[A/G]GGTAGACGACTCTGT | 138151 |
rs10481730 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136043985 | gtgcatcaccacacc[C/T]ggctaatttttgtat | 138151 |
rs10540260 | in-del | -/T | 0.49423 | 0.0534032 | intron-variant | NACC2 | GRCh38.p7 | 9:136079059 | AATCATAGCTTCTTC[-/T]TTTTTTTTTTTTTAA | 138151 |
rs10597829 | in-del | -/CAGGA | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136062172 | CAGGACAGGACAGGA[-/CAGGA]AAGGAAAGAGAGAGA | 138151 |
rs10623394 | snp | C/G | 0.5 | 0 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007544 | AGACGTGCACACACA[C/G]ACACGCACACACACA | 138151 |
rs10735244 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136081068 | AGGGTCACGGATCAC[A/G]AACGGCTGCGGGGAG | 138151 |
rs10745379 | snp | A/G | 0.498794 | 0.0245311 | intron-variant | NACC2 | GRCh38.p7 | 9:136019638 | GTGCACCAGGGTCAC[A/G]ACGAGAGGGCCCGGA | 138151 |
rs10745380 | snp | C/T | 0.143622 | 0.226238 | intron-variant | NACC2 | GRCh38.p7 | 9:136081015 | GATTAACAGAGGTGA[C/T]GGAGGAGGAAGTTTT | 138151 |
rs10776866 | snp | A/G | 0.49928 | 0.018956 | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006326 | CCTTGTAAAACACTG[A/G]GGAGAGCAAGAGATG | 138151 |
rs10776867 | snp | A/G | 0.331411 | 0.236373 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007784 | TGCCAAGATGTTTCC[A/G]TAAAAATTTCCCTTT | 138151 |
rs10776868 | snp | A/G | 0.266 | 0.249487 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009424 | CACTGAGCCACCTGC[A/G]GCCCTAGGAATGCAG | 138151 |
rs10776870 | snp | C/T | 0.364609 | 0.222182 | intron-variant | NACC2 | GRCh38.p7 | 9:136019585 | GAGCAATGAGCTAAC[C/T]GCATGGAGGTGAACA | 138151 |
rs10776871 | snp | A/G | 0.293551 | 0.246177 | intron-variant | NACC2 | GRCh38.p7 | 9:136062665 | CATGCCTGTAATCCC[A/G]ACATTTTGGGAGGTC | 138151 |
rs10776872 | snp | A/G | 0.41325 | 0.18934 | intron-variant | NACC2 | GRCh38.p7 | 9:136062692 | GGTCAGCGGGGGTGG[A/G]CTGCTTGAGCCCAGC | 138151 |
rs10776873 | snp | C/T | 0.321292 | 0.23962 | intron-variant | NACC2 | GRCh38.p7 | 9:136062740 | GGCAACATGGCGAAA[C/T]CCCATCTCTACAAAA | 138151 |
rs10776874 | snp | G/T | 0.296109 | 0.245711 | intron-variant | NACC2 | GRCh38.p7 | 9:136062844 | ATCACCTAAGCCTGG[G/T]AGGCCGAGGCCGCAG | 138151 |
rs10776875 | snp | A/G | 0.499918 | 0.00638925 | intron-variant | NACC2 | GRCh38.p7 | 9:136073046 | CTCAGCACAAGACAC[A/G]GGTAATGGGATGAAA | 138151 |
rs10776876 | snp | C/T | 0.391954 | 0.205789 | intron-variant | NACC2 | GRCh38.p7 | 9:136073424 | GACAGAGCAAGACTG[C/T]CTCAAAAAAAAAATT | 138151 |
rs10776877 | snp | C/T | 0.409552 | 0.192466 | intron-variant | NACC2 | GRCh38.p7 | 9:136074022 | AAAAAAATTAAGATC[C/T]TGGCCGGGCACAGTG | 138151 |
rs10776878 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074464 | TCTCAAAAAAAAAAA[A/G]AAAAAAGAAGAAAAA | 138151 |
rs10776879 | snp | A/C | 0.486984 | 0.079614 | intron-variant | NACC2 | GRCh38.p7 | 9:136081329 | CCTGCACACCACACA[A/C]CCCCAACCAAGATGA | 138151 |
rs10776880 | snp | G/T | 0.499968 | 0.00399348 | intron-variant | NACC2 | GRCh38.p7 | 9:136083360 | TCCCAGGCTGGGTTG[G/T]GGGGGAGGCAGCCAC | 138151 |
rs10776881 | snp | C/T | 0.0995161 | 0.199636 | intron-variant | NACC2 | GRCh38.p7 | 9:136087034 | GGGTGGACCCTAACA[C/T]GCATCCTTACAGAAG | 138151 |
rs10858200 | snp | A/G | 0.16618 | 0.23553 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008993 | CGGGACATTGTGCGG[A/G]CCTGAACAGCAGTCA | 138151 |
rs10858201 | snp | A/G | 0.336245 | 0.234652 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015268 | CGCGTGGGCACCTGC[A/G]CCCCAGAGCCCAACC | 138151 |
rs10858202 | snp | C/T | 0.38821 | 0.208322 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015345 | ATCCAGAAGCAGTGC[C/T]GGGGCAGGGTGGGAG | 138151 |
rs10858203 | snp | C/T | 0.322721 | 0.23919 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015383 | CACAGCAAGGTGGGC[C/T]CCTACCCCTCCTGGC | 138151 |
rs10858204 | snp | A/G | 0.42574 | 0.177808 | intron-variant | NACC2 | GRCh38.p7 | 9:136016858 | GGAGGACGGCTTGGC[A/G]GGGCCAGCAGGGCAG | 138151 |
rs10858205 | snp | A/G | 0.498774 | 0.02473 | intron-variant | NACC2 | GRCh38.p7 | 9:136017523 | TTGCCCCCCACCCCC[A/G]CCACCCTGAGTCCCA | 138151 |
rs10858206 | snp | C/T | 0.279991 | 0.248195 | intron-variant | NACC2 | GRCh38.p7 | 9:136025829 | TGGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG | 138151 |
rs10858207 | snp | C/T | 0.378962 | 0.21417 | intron-variant | NACC2 | GRCh38.p7 | 9:136027288 | CCCAAGAGAAAACCT[C/T]AAACAAGAGGACAAA | 138151 |
rs10858208 | snp | C/T | 0.36955 | 0.219562 | intron-variant | NACC2 | GRCh38.p7 | 9:136028970 | GCACAAGAGGGAGGC[C/T]GAGGTGGGGCTAACA | 138151 |
rs10858209 | snp | A/G | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136035355 | GAAGGTTCCGCTGCT[A/G]TGAATTGCAGCTGAA | 138151 |
rs10858212 | snp | G/T | 0.48 | 0.0979796 | intron-variant | NACC2 | GRCh38.p7 | 9:136038594 | TTGTACATCAAAGAG[G/T]AAATGTTATAATATG | 138151 |
rs10858213 | snp | C/T | 0.41325 | 0.18934 | intron-variant | NACC2 | GRCh38.p7 | 9:136063059 | ACTGTTTTCTTCTAA[C/T]TTTTGTTCTCGTTGT | 138151 |
rs10858214 | snp | A/G | 0.294832 | 0.245947 | intron-variant | NACC2 | GRCh38.p7 | 9:136063867 | ccagcctgggaaaca[A/G]agcgagactccatct | 138151 |
rs10858215 | snp | A/G | 0.309648 | 0.24278 | intron-variant | NACC2 | GRCh38.p7 | 9:136063871 | cctgggaaacagagc[A/G]agactccatctcaaa | 138151 |
rs10858216 | snp | A/G | 0.43655 | 0.16643 | intron-variant | NACC2 | GRCh38.p7 | 9:136066494 | TATAATCAAAAAGAC[A/G]GAAAACAAAGGTTGG | 138151 |
rs10858218 | snp | A/G | 0.474363 | 0.110278 | intron-variant | NACC2 | GRCh38.p7 | 9:136071145 | GGTTGAGGCAGGAGA[A/G]TCGCTTGAACCTGGG | 138151 |
rs10858220 | snp | A/T | 0.465996 | 0.12588 | intron-variant | NACC2 | GRCh38.p7 | 9:136073438 | GTCTCAAAAAAAAAA[A/T]TTTTAATAAAAAATA | 138151 |
rs10858221 | snp | A/T | 0.31503 | 0.241394 | intron-variant | NACC2 | GRCh38.p7 | 9:136077917 | ATAATATCAGTCCAA[A/T]CATAGTTTTGTTTTG | 138151 |
rs10858222 | snp | A/G | 0.387832 | 0.208572 | intron-variant | NACC2 | GRCh38.p7 | 9:136093795 | CGGTGGCCGGGAGAA[A/G]AAGGGGTGGGTGGCT | 138151 |
rs11103262 | snp | A/G | 0.232943 | 0.249417 | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006408 | AGCTGGCCTGGGGAC[A/G]CCGCTAACAGGGACG | 138151 |
rs11103263 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007453 | gacgcgcacacacac[A/G]cgcacacagacgcac | 138151 |
rs11103264 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007513 | cacatgcacagacgc[A/G]cacacacagacgcac | 138151 |
rs11103265 | snp | A/G | 0 | 0 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007533 | cacagacgcacagac[A/G]tgcacacacagacac | 138151 |
rs11103266 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007534 | acagacgcacagacg[C/T]gcacacacagacacg | 138151 |
rs11103268 | snp | C/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007546 | ACGTGCACACACAGA[C/G]ACGCACACACACACA | 138151 |
rs11103269 | snp | C/T | 0.49823 | 0.0296997 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007554 | ACACAGACACGCACA[C/T]ACACACAGACACGCG | 138151 |
rs11103270 | snp | A/T | 0.0879971 | 0.190408 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007616 | GGCTGACATGACAAA[A/T]GTATGCAGCAGCAAC | 138151 |
rs11103271 | snp | A/G | 0.0138799 | 0.0821421 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007752 | GGTTCATGGGCCATA[A/G]ATCTTTTTCCACTTG | 138151 |
rs11103272 | snp | C/T | 0.349671 | 0.229272 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010929 | CCCTCACCACACCCC[C/T]GCACACACACGCACA | 138151 |
rs11103273 | snp | C/T | 0.0490535 | 0.14873 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014038 | GAAGAGGCGCACAGA[C/T]GGGTGAGGGGGAGGG | 138151 |
rs11103274 | snp | A/G | 0.295599 | 0.245806 | intron-variant | NACC2 | GRCh38.p7 | 9:136017111 | CCAATAGCCAGGCTG[A/G]CCGACACGCCACCGC | 138151 |
rs11103275 | snp | A/G | 0.266819 | 0.249434 | intron-variant | NACC2 | GRCh38.p7 | 9:136018748 | AGCCCAGAATTACCC[A/G]AGTGCTCAGGGAACA | 138151 |
rs11103277 | snp | C/G | 0.303187 | 0.244277 | intron-variant | NACC2 | GRCh38.p7 | 9:136020588 | CCCTAAAAGTGTATA[C/G]CATTTGTTAAAATGC | 138151 |
rs11103278 | snp | C/G | 0.0599851 | 0.162463 | intron-variant | NACC2 | GRCh38.p7 | 9:136023652 | CTGATCTGATGGCAT[C/G]CCTTTCCTGCTCTAC | 138151 |
rs11103279 | snp | G/T | 0.302324 | 0.24856 | intron-variant | NACC2 | GRCh38.p7 | 9:136032011 | GCAAGGGTCGTCCTC[G/T]GCAGCACCCCTGGTG | 138151 |
rs11103281 | snp | C/T | 0.111928 | 0.208413 | intron-variant | NACC2 | GRCh38.p7 | 9:136038210 | TGTTCTATATCTTGA[C/T]TGGGGAGGTGACTAC | 138151 |
rs11103282 | snp | C/T | 0.220544 | 0.248259 | intron-variant | NACC2 | GRCh38.p7 | 9:136038351 | GACCAGCCTGGGCAA[C/T]GTGCTGAAATCCTGT | 138151 |
rs11103283 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136042741 | ACACAGACACACACA[C/G]ACACAGAGACAGAGA | 138151 |
rs11103284 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136042757 | ACACAGAGACAGAGA[C/G]ACACACACAGAGACA | 138151 |
rs11103285 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136042767 | AGAGACACACACACA[C/G]AGACACACAGACACA | 138151 |
rs11103286 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136042771 | ACACACACACAGAGA[C/G]ACACAGACACACACA | 138151 |
rs11103287 | snp | C/G | 0.0637235 | 0.166737 | intron-variant | NACC2 | GRCh38.p7 | 9:136042777 | ACACAGAGACACACA[C/G]ACACACACACACATA | 138151 |
rs11103288 | snp | A/G | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136044585 | TGGGTGGTGGTGGGG[A/G]GGCTCTAACAGTGCG | 138151 |
rs11103289 | snp | A/G | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136047043 | CCTCTCACTCAACAG[A/G]TAGGGAGACTGAGGC | 138151 |
rs11103291 | snp | A/G | 0.372592 | 0.217879 | intron-variant | NACC2 | GRCh38.p7 | 9:136055953 | GTCAGCAGGAGCACA[A/G]GGGGTGTTAGGAATA | 138151 |
rs11103292 | snp | C/T | 0.108048 | 0.20579 | intron-variant | NACC2 | GRCh38.p7 | 9:136058724 | CACGTATCTCTGAAT[C/T]GAAAATAAAAGTTGA | 138151 |
rs11103293 | snp | A/G | 0.434253 | 0.168969 | intron-variant | NACC2 | GRCh38.p7 | 9:136058771 | AACTCACACAGCACC[A/G]GAGATTCGGAATAGC | 138151 |
rs11103294 | snp | C/T | 0.292008 | 0.246445 | intron-variant | NACC2 | GRCh38.p7 | 9:136059167 | TTTAGCTGGGACATC[C/T]GGGGGCAAAACTGCC | 138151 |
rs11103295 | snp | C/T | 0.279461 | 0.248258 | intron-variant | NACC2 | GRCh38.p7 | 9:136060771 | TCAGAGCCCTGGGCA[C/T]GTCCCCACCAGCCTG | 138151 |
rs11103296 | snp | C/G | 0.279726 | 0.248226 | intron-variant | NACC2 | GRCh38.p7 | 9:136060921 | GTCCCTGAGAGACTG[C/G]GTACAGGGGTCCGGG | 138151 |
rs11103297 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | NACC2 | GRCh38.p7 | 9:136061110 | ATGCCAGGTAAGGGG[C/T]TCCTCTTCTGCCTCC | 138151 |
rs11103298 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | NACC2 | GRCh38.p7 | 9:136061153 | CCCCTAAACCCCATC[C/T]GGGTCTGCACAGCCC | 138151 |
rs11103299 | snp | G/T | 0.279726 | 0.248226 | intron-variant | NACC2 | GRCh38.p7 | 9:136061156 | CTAAACCCCATCCGG[G/T]TCTGCACAGCCCCCA | 138151 |
rs11103302 | snp | A/G | 0.424503 | 0.179021 | intron-variant | NACC2 | GRCh38.p7 | 9:136066706 | CTAGCAGTATCATTT[A/G]CAATAGCCAAGAAGT | 138151 |
rs11103305 | snp | C/T | 0.393619 | 0.204631 | intron-variant | NACC2 | GRCh38.p7 | 9:136069590 | aaacaaaaaaaacaC[C/T]Tcacttcaaatataa | 138151 |
rs11103306 | snp | A/G | 0.381308 | 0.21274 | intron-variant | NACC2 | GRCh38.p7 | 9:136069876 | CTAGTAGAGACTTCA[A/G]CAGCCTTCTCTAAAC | 138151 |
rs11103307 | snp | C/T | 0.495891 | 0.0451408 | intron-variant | NACC2 | GRCh38.p7 | 9:136070608 | TATAGCATTAATGGA[C/T]GTATTAGAAAAAAGG | 138151 |
rs11103309 | snp | C/T | 0.496616 | 0.0409947 | intron-variant | NACC2 | GRCh38.p7 | 9:136071859 | TCAGGGGAGAAGAGC[C/T]GGCCTTTGAAGCCAA | 138151 |
rs11103310 | snp | C/T | 0.496649 | 0.0407971 | intron-variant | NACC2 | GRCh38.p7 | 9:136072155 | AGGCAGGAGAATTAC[C/T]TGAAACCGGGAGGCG | 138151 |
rs11103311 | snp | A/G | 0.375 | 0.216506 | intron-variant | NACC2 | GRCh38.p7 | 9:136074177 | CAGGCATGGCCAGGC[A/G]CGGTGGCTCATGCCT | 138151 |
rs11103312 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | NACC2 | GRCh38.p7 | 9:136074216 | agcactttgggaggc[C/T]gaggagggcagatca | 138151 |
rs11103313 | snp | G/T | 0.420415 | 0.182917 | intron-variant | NACC2 | GRCh38.p7 | 9:136077923 | TCAGTCCAATCATAG[G/T]TTTGTTTTGGGTTTT | 138151 |
rs11103314 | snp | C/T | 0.419936 | 0.183362 | intron-variant | NACC2 | GRCh38.p7 | 9:136077975 | GACGGGGTTTCACCA[C/T]GTTAGCCAGGCTGGT | 138151 |
rs11103315 | snp | A/G | 0.499918 | 0.00638925 | intron-variant | NACC2 | GRCh38.p7 | 9:136079395 | CACAGGATGCCAACT[A/G]CAGAAGCCAATGCGT | 138151 |
rs11103316 | snp | C/G | 0.229723 | 0.249176 | intron-variant | NACC2 | GRCh38.p7 | 9:136079653 | GCTCCTTCCTGGGGC[C/G]CTGCCGTGGCCGGCA | 138151 |
rs11103317 | snp | A/G | 0.229723 | 0.249176 | intron-variant | NACC2 | GRCh38.p7 | 9:136079665 | GGCCCTGCCGTGGCC[A/G]GCACTCCCCGAATGC | 138151 |
rs11103318 | snp | A/T | 0.499961 | 0.0043928 | intron-variant | NACC2 | GRCh38.p7 | 9:136080858 | GCGCAAACTCCAGCC[A/T]GCTGCATCAGGCCCC | 138151 |
rs11103319 | snp | A/C | 0.499859 | 0.0083854 | intron-variant | NACC2 | GRCh38.p7 | 9:136082017 | GCCAATCTGCCCTGG[A/C]CAGGGCCTCCAACCT | 138151 |
rs11103320 | snp | A/G | 0.412583 | 0.189912 | intron-variant | NACC2 | GRCh38.p7 | 9:136082246 | CATCGGTGTGGCCAC[A/G]CCACGGCCTGATGGA | 138151 |
rs11103321 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136085164 | ttttttttttttttt[G/T]gcgagactgagtttc | 138151 |
rs11103322 | snp | A/C | 0.490007 | 0.0699769 | intron-variant | NACC2 | GRCh38.p7 | 9:136088374 | CTCTCCCCTAGGGCA[A/C]AAATTTGAGTCCACA | 138151 |
rs11103323 | snp | C/T | 0.490007 | 0.0699769 | intron-variant | NACC2 | GRCh38.p7 | 9:136088431 | CCACATCTTTCCCAG[C/T]AGCTGCCCCTGAGCC | 138151 |
rs11103324 | snp | C/T | 0.372794 | 0.217765 | intron-variant | NACC2 | GRCh38.p7 | 9:136089200 | GCCCCCACCCAGAGC[C/T]TCCCCCTGCCAGGGG | 138151 |
rs11103325 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136089528 | TTAGCCCCTCCCCCA[C/G]CGCTGGGGGCCTCTC | 138151 |
rs11103326 | snp | C/T | 0.422787 | 0.180679 | intron-variant | NACC2 | GRCh38.p7 | 9:136091600 | ATACTTCCAGACAGA[C/T]GCCTTCACGCCTGCC | 138151 |
rs11103327 | snp | A/G | 0.0755793 | 0.179102 | intron-variant | NACC2 | GRCh38.p7 | 9:136094952 | gcgggcgcctccgcc[A/G]ggaccccccggcccc | 138151 |
rs11103328 | snp | G/T | 0.289165 | 0.246913 | intron-variant | NACC2 | GRCh38.p7 | 9:136094968 | ggaccccccggcccc[G/T]cccggcccccctccg | 138151 |
rs11273841 | in-del | -/AAACCCCTACT | 0.302435 | 0.244439 | intron-variant | NACC2 | GRCh38.p7 | 9:136033465 | CCAGCGAACATGGTG[-/AAACCCCTACT]AAACCCCTACTAAAC | 138151 |
rs11286661 | in-del | -/C | 0.25214 | 0.249991 | intron-variant | NACC2 | GRCh38.p7 | 9:136032018 | TCGTCCTCGGCAGCA[-/C]CCCTGGTGATCACTG | 138151 |
rs11301582 | in-del | -/G | 0.370365 | 0.219117 | intron-variant | NACC2 | GRCh38.p7 | 9:136083359 | TTCCCAGGCTGGGTT[-/G]GGGGGGAGGCAGCCA | 138151 |
rs11315582 | in-del | -/A | 0.490063 | 0.0697833 | intron-variant | NACC2 | GRCh38.p7 | 9:136063884 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAACA | 138151 |
rs11375504 | in-del | -/T | 0.095934 | 0.196885 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014994 | TGTCCTGAAGGACAC[-/T]GATGTCCAGGTGCGC | 138151 |
rs11442793 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136089996 | ATCCAAAAAAAAAAA[-/A]GAATAAACTGCTGAC | 138151 |
rs11507053 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136041001 | AAGGAAAGGAAGGAA[A/G]GAAAGGAAGGAAGGA | 138151 |
rs11515614 | snp | A/C | 0.31721 | 0.240796 | intron-variant | NACC2 | GRCh38.p7 | 9:136068659 | GACTATATACTAAAA[A/C]CCACTAAATTATACA | 138151 |
rs11562367 | snp | C/T | 0.494187 | 0.0535994 | intron-variant | NACC2 | GRCh38.p7 | 9:136068877 | TCCATTAAATGTAAA[C/T]GATCTAAATACACCC | 138151 |
rs11787554 | snp | A/T | | | intron-variant, upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136051919 | aggaggagatggtgg[A/T]ggaggaggaggagga | 138151 |
rs11789434 | snp | G/T | 0.499866 | 0.0081858 | intron-variant | NACC2 | GRCh38.p7 | 9:136082642 | CCACCCGCCAGGCCC[G/T]CGCTGCCTCCACGGA | 138151 |
rs11792837 | snp | A/C | 0.231189 | 0.249291 | intron-variant | NACC2 | GRCh38.p7 | 9:136080936 | AGTAGGTCGGGGGGA[A/C]ACAGGCCTGGGACAG | 138151 |
rs11793070 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | NACC2 | GRCh38.p7 | 9:136083009 | CATAACTTCTGCCCC[A/C]TTAGACATCTACACT | 138151 |
rs11999397 | snp | C/G | 0.131723 | 0.220251 | intron-variant | NACC2 | GRCh38.p7 | 9:136079824 | CCAGGACAGGCAGCA[C/G]CCGGGGAAGTCTCAA | 138151 |
rs12000338 | snp | A/C/T | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136069380 | atggtgaaacccctt[A/C/T]tctactaaaaataca | 138151 |
rs12003436 | snp | A/G | 0.0663309 | 0.169604 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013433 | GTGTCCCAGTGGCAG[A/G]AGCCGGCCCAGCCAC | 138151 |
rs12003954 | snp | C/T | 0.093777 | 0.195178 | intron-variant | NACC2 | GRCh38.p7 | 9:136081154 | GAAGCCCAGACCAAA[C/T]GGACCCTCAGTGGCC | 138151 |
rs12003965 | snp | C/T | 0.130351 | 0.219509 | intron-variant | NACC2 | GRCh38.p7 | 9:136081256 | GGGCACTGGGGGCTC[C/T]GCAGGACAGGGCAGG | 138151 |
rs12004030 | snp | C/G | 0.23846 | 0.249734 | intron-variant | NACC2 | GRCh38.p7 | 9:136039044 | gcagactgttagact[C/G]cataaaaatgcaaat | 138151 |
rs12004973 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | NACC2 | GRCh38.p7 | 9:136019032 | GCACCAGAGCGGCCA[A/G]AAAAGCCTCTTCTAT | 138151 |
rs12006463 | snp | G/T | 0.148326 | 0.228391 | intron-variant | NACC2 | GRCh38.p7 | 9:136081234 | ACCAGGTGGACTCAG[G/T]CCCGACGGGCACTGG | 138151 |
rs12115575 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | NACC2 | GRCh38.p7 | 9:136037827 | ttttcatttctattg[G/T]gtcaattaacctaag | 138151 |
rs12235121 | snp | G/T | 0.252702 | 0.249985 | intron-variant | NACC2 | GRCh38.p7 | 9:136024181 | GTGTGTGTGTGTGAG[G/T]ACGGAGTGTGTGTGT | 138151 |
rs12337512 | snp | C/T | 0.130008 | 0.219321 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013374 | CCGCCCGCACGAATG[C/T]CCTGCTGGGAGGCCA | 138151 |
rs12337940 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | NACC2 | GRCh38.p7 | 9:136056159 | TGCCCAGCTCCGGAT[A/G]TGCCAGGGCCTCAGG | 138151 |
rs12338232 | snp | C/G | 0.0577344 | 0.159793 | intron-variant | NACC2 | GRCh38.p7 | 9:136081000 | CCCCAAGCACATTCT[C/G]ATTAACAGAGGTGAT | 138151 |
rs12338792 | snp | C/G/T | 0.444444 | 0.157135 | intron-variant | NACC2 | GRCh38.p7 | 9:136074427 | CACTGCACTCCAGCC[C/G/T]GGGCGACAGAGCAAG | 138151 |
rs12340397 | snp | A/G | 0.29175 | 0.246489 | intron-variant | NACC2 | GRCh38.p7 | 9:136057703 | CCGGCTCGGCCGGGT[A/G]GAAGCTGAGATTGGG | 138151 |
rs12342424 | snp | A/T | 0.11228 | 0.208646 | intron-variant | NACC2 | GRCh38.p7 | 9:136037938 | tcataattattaaaa[A/T]cctaatgtcctttaa | 138151 |
rs12343487 | snp | A/C | 0.492188 | 0.0620098 | intron-variant | NACC2 | GRCh38.p7 | 9:136074369 | GAGGCAGGAGAATGG[A/C]GTGAACCCGGGAGGC | 138151 |
rs12344535 | snp | G/T | 0.492188 | 0.0620098 | intron-variant | NACC2 | GRCh38.p7 | 9:136074391 | CCGGGAGGCGGAGCT[G/T]GCAGTGAGCCGAGGT | 138151 |
rs12345528 | snp | A/G | 0.22263 | 0.248497 | intron-variant | NACC2 | GRCh38.p7 | 9:136067610 | tgggaagccaaggcg[A/G]gcagatcacgaggtc | 138151 |
rs12346383 | snp | C/T | 0.220567 | 0.248261 | intron-variant | NACC2 | GRCh38.p7 | 9:136019795 | GGGACCCAGAAGGAG[C/T]CCCCGCCGTACCTTC | 138151 |
rs12349022 | snp | A/G | 0.0611083 | 0.163768 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015476 | CCTGGCAGCTGGAAG[A/G]CGAGGCCAGCCCAGG | 138151 |
rs12349461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136062865 | gaggccgcagtgtgc[C/T]gtgatcgtgccactg | 138151 |
rs12350140 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136046046 | AATGAAGGCGGGTAC[A/G]CGAGGAAGAGGGCCC | 138151 |
rs12375829 | snp | C/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007556 | acagacacgcacaca[C/G]acacagacacgcgca | 138151 |
rs12376241 | snp | C/G | 0.372592 | 0.217879 | intron-variant | NACC2 | GRCh38.p7 | 9:136026294 | GTTGCAGTGAACCAA[C/G]ATGGCACCACTGCAC | 138151 |
rs12376616 | snp | C/T | 0.342806 | 0.232136 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009203 | ACTCCAGAGGGAACT[C/T]AAGTGCAGCTCAACC | 138151 |
rs12377266 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007517 | tgcacagacgcgcac[A/G]cacagacgcacagac | 138151 |
rs12377357 | snp | A/T | 0.27893 | 0.24832 | intron-variant | NACC2 | GRCh38.p7 | 9:136032433 | AATTTCCTTAATCTG[A/T]TAAAATGTATCACAG | 138151 |
rs12378498 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007549 | tgcacacacagacac[A/G]cacacacacacagac | 138151 |
rs12378820 | snp | C/G | 0 | 0 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007823 | CCCAGGCAGTACACG[C/G]CTGGGTGGGGTGGGG | 138151 |
rs12380336 | snp | C/T | 0.355525 | 0.226637 | intron-variant | NACC2 | GRCh38.p7 | 9:136085125 | gcaacataggaagac[C/T]ccatttctacaattt | 138151 |
rs12552062 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136044720 | CCCCAAACAACAGTC[C/T]TGAGTTTTGAGCTGC | 138151 |
rs12553218 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136048203 | GACAGAGCTCCTTCC[C/G]AACAGGGGCCCTGGG | 138151 |
rs12682934 | snp | C/T | 0.181659 | 0.240478 | intron-variant | NACC2 | GRCh38.p7 | 9:136067559 | cgatgctcgatgggc[C/T]gggcgcggtggctca | 138151 |
rs12685144 | snp | A/G | 0.337158 | 0.234315 | intron-variant | NACC2 | GRCh38.p7 | 9:136067790 | cggtgagccgagatc[A/G]cggcactgcctccag | 138151 |
rs12685145 | snp | A/G | 0.276534 | 0.248588 | intron-variant | NACC2 | GRCh38.p7 | 9:136067825 | gcaacagggcgagac[A/G]ccatctcaaaaacac | 138151 |
rs13283561 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | NACC2 | GRCh38.p7 | 9:136083725 | gcttttggcctccac[C/T]gctgtgcaagaagaa | 138151 |
rs13285151 | snp | C/T | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136054664 | CAGACATCAGGGCAT[C/T]CCCACCCTCCCCTGC | 138151 |
rs13286979 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136075782 | CGGTGAAACCTCAGA[G/T]ACAGGGGTCTTGGGT | 138151 |
rs13290816 | snp | C/T | 0.0456336 | 0.143994 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011111 | TCAGTGACGCACAGC[C/T]CAGCCCCCTCGCCAC | 138151 |
rs13293625 | snp | A/G | 0.323434 | 0.238972 | intron-variant | NACC2 | GRCh38.p7 | 9:136017185 | CGACAAACCACTGCT[A/G]GGGCAGATGACGGCC | 138151 |
rs13296635 | snp | C/G | | | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014057 | tgagggggagggggg[C/G]aggtggagggggagg | 138151 |
rs13296783 | snp | C/G | | | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014092 | gCTGGAAGCTTCTAG[C/G]ACTTTTTTTGGGGAG | 138151 |
rs13298848 | snp | A/G | 0.429087 | 0.174436 | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014299 | CTCAGCTCCCTCCCC[A/G]AGAACACACTTTGTT | 138151 |
rs13302142 | snp | C/T | 0.401392 | 0.198948 | intron-variant | NACC2 | GRCh38.p7 | 9:136057686 | GTAGGGTCTCCCCTG[C/T]ACCGGCTCGGCCGGG | 138151 |
rs13302701 | snp | C/G/T | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136074321 | AGCCGGGCATGGTGG[C/G/T]GGGCGCCTGTAGTCC | 138151 |
rs13439890 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136054380 | CAGGCCACCTGCACC[A/G]GTGAGGCTGCAGCCC | 138151 |
rs17040637 | snp | C/T | 0.046775 | 0.145601 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015870 | TTCTGGACTCGGACG[C/T]GTTTGTTCTGCCAGA | 138151 |
rs17040643 | snp | C/G | 0.321769 | 0.239477 | intron-variant | NACC2 | GRCh38.p7 | 9:136025310 | CTGCTTACGACTCCT[C/G]ACCTGTTTTCACACG | 138151 |
rs28436969 | snp | A/C | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007536 | AGACGCACAGACGTG[A/C]ACACACAGACACGCA | 138151 |
rs28488209 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | NACC2 | GRCh38.p7 | 9:136025614 | GGGATTAAGTCCTAT[C/T]AAAAAAAAAAAAAAC | 138151 |
rs28573817 | snp | A/G/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007575 | CAGACACGCGCACAC[A/G/T]CACACTCTCACCCAC | 138151 |
rs28608535 | snp | G/T | 0.0611083 | 0.163768 | intron-variant | NACC2 | GRCh38.p7 | 9:136017384 | TCATGGAGGGCCAGG[G/T]CTGAGACCCCTCATC | 138151 |
rs28688660 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NACC2 | GRCh38.p7 | 9:136081357 | TGAAGCCAGCCACCC[A/G]CTGGGCTCCCCATGG | 138151 |
rs28802304 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136041089 | AGGAAAGGAAGGAAG[C/G]AAAGGAAAGGAAAGG | 138151 |
rs28865956 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136041077 | AGGAAGGAAGGAAGG[A/G]AAGGAAGGAAGCAAA | 138151 |
rs28871643 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136041075 | AAAGGAAGGAAGGAA[A/G]GAAAGGAAGGAAGCA | 138151 |
rs28885459 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136070680 | TCAGAAAAAAAAAAA[A/C]CAAAAACCAAAAACT | 138151 |
rs28886130 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136041038 | AGGAAAGAAGGAAAG[A/G]AAAGGAAGGAAGGAA | 138151 |
rs33916861 | in-del | -/T | 0.483272 | 0.0899109 | intron-variant | NACC2 | GRCh38.p7 | 9:136090870 | TCTCTGCAGCATGGC[-/T]TTGCCGTTCACCCCA | 138151 |
rs34024892 | in-del | -/A | 0.392303 | 0.220134 | intron-variant | NACC2 | GRCh38.p7 | 9:136065811 | AGAGACCCTGTCTCC[-/A]AAAAAAAAAAAAGAA | 138151 |
rs34055916 | in-del | -/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136073538 | TAGTCCTGCCCATCA[-/G]GGGGAGAAGAGGCGC | 138151 |
rs34087690 | in-del | -/A | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136071544 | TGAGACTCCATCTCA[-/A]AAAAAAAAAAAAAAA | 138151 |
rs34114062 | in-del | -/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136027277 | TAAAACAAAACCCAA[-/G]GAGAAAACCTCAAAC | 138151 |
rs34315455 | in-del | -/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136019774 | GGCGCGGGGTTGGGG[-/C]CTTCAGGGACCCAGA | 138151 |
rs34514433 | in-del | -/AAA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136026365 | AAAAAAAAAAAAAAA[-/AAA]GATAAAAGAATAGAA | 138151 |
rs34645891 | in-del | -/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136071962 | TACCCAAAGGCCAGG[-/C]CACGGTGGCTCGAGT | 138151 |
rs34696092 | snp | C/T | 0.078151 | 0.181571 | intron-variant | NACC2 | GRCh38.p7 | 9:136065680 | GAGTGGTGGCACATG[C/T]CTGTAGTCCCAGCTA | 138151 |
rs34755994 | in-del | -/A | 0.214239 | 0.247429 | intron-variant | NACC2 | GRCh38.p7 | 9:136070669 | ATCTCAAGGAATCAG[-/A]AAAAAAAAAAACAAA | 138151 |
rs34846745 | in-del | -/AATC | 0.498734 | 0.0251279 | intron-variant | NACC2 | GRCh38.p7 | 9:136017809 | CTGCCTTCACTAGGG[-/AATC]AATCCCACTGCCCTG | 138151 |
rs34877631 | in-del | -/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136081393 | CCCACCCGCTCACAG[-/T]CCATGGTTCCCATCC | 138151 |
rs34902301 | in-del | -/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136065344 | AATAATTAGGCTGGG[-/C]CGTGGTGGCTCACAC | 138151 |
rs34933502 | in-del | -/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136022467 | GGGCCGGCTGTGGGG[-/C]CAACTGGTGCAGACG | 138151 |
rs34934470 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136090143 | TTCAGCAAAGATGGT[-/A]CTTCCCCTTTCTTGG | 138151 |
rs34955493 | in-del | -/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136060546 | ACACTGGGGCCGGGT[-/G]GGGGGGTGCCACTCT | 138151 |
rs35009638 | in-del | -/T/TTT | 0.484701 | 0.0861117 | intron-variant | NACC2 | GRCh38.p7 | 9:136068919 | AGATTGAAAGAATAC[-/T/TTT]TTTTTTTTTTTTTTA | 138151 |
rs35027341 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136073428 | GAGCAAGACTGTCTC[-/A]AAAAAAAAAATTTTA | 138151 |
rs35034816 | snp | C/T | 0.39214 | 0.205661 | intron-variant | NACC2 | GRCh38.p7 | 9:136064286 | AGAGTGAGGCCCTGC[C/T]TCAAAAAAAAGACAA | 138151 |
rs35046824 | in-del | -/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136029861 | TCTGTGCCTGGCTCA[-/C]CCTCAGAGGTGTGGG | 138151 |
rs35160466 | snp | A/G | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136023061 | GAAGGAGGGAGGAAG[A/G]AGGGAAGAGGGAGGG | 138151 |
rs35237048 | in-del | -/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136059976 | ACGGGGAGCCGCCTC[-/G]GGGGGACCTGCAGGA | 138151 |
rs35317169 | in-del | -/T | 0.499992 | 0.00199679 | intron-variant | NACC2 | GRCh38.p7 | 9:136022924 | GCCACACCGTGCCTG[-/T]TAAGACACAGCCCGT | 138151 |
rs35455166 | in-del | -/TG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024504 | TGTGTGAGGACAGAA[-/TG]TGTGTGTGTGTGTGT | 138151 |
rs35501494 | in-del | -/CT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136064395 | AAATCACAAGTATTT[-/CT]CTCTACACTTGCAAT | 138151 |
rs35535099 | in-del | -/T | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136097207 | AGCTCTGTTTATTCC[-/T]TTTTTTTTTTTTTTT | 138151 |
rs35564918 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136066193 | GTGAAACCCCATCTC[-/A]AAAAAAAAAAAAGAA | 138151 |
rs35675747 | snp | C/T | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136077726 | GGGACCCCAAGGACT[C/T]TGGCCACCCCCACAC | 138151 |
rs35709910 | in-del | -/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136032329 | CAGAGGAAAACCACA[-/G]GGACTGTTACAATGC | 138151 |
rs35734501 | in-del | -/A | 0.348574 | 0.229746 | intron-variant | NACC2 | GRCh38.p7 | 9:136067618 | CAAGGCGGGCAGATC[-/A]CGAGGTCAAGAGATC | 138151 |
rs35735912 | in-del | -/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136059963 | CTCCTCAGGGCGCAC[-/G]GGGGAGCCGCCTCGG | 138151 |
rs35761033 | in-del | -/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136090593 | CCATGAGGGACCCCA[-/G]GCAGCTCTGGCCAAC | 138151 |
rs35835119 | in-del | -/A | 0.282632 | 0.247861 | intron-variant | NACC2 | GRCh38.p7 | 9:136074452 | TCTCAAAAAAAAAAA[-/A]GAAAAAAGAAGAAAA | 138151 |
rs35881908 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136026367 | AAAAAAAAAAAAAAA[-/A]GATAAAAGAATAGAA | 138151 |
rs35899937 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136083229 | CTGGTGGGGGTCAGA[A/G]CCCCTGGGGAGCTGC | 138151 |
rs35947673 | snp | A/G | 0.323908 | 0.238825 | intron-variant | NACC2 | GRCh38.p7 | 9:136019067 | GCCTTGCCGTGCACC[A/G]GGTGCTGCTGGCTAA | 138151 |
rs35963075 | in-del | -/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136027472 | ATATACAGGGGCTCA[-/G]GGGAAAGTCTCAACA | 138151 |
rs36038386 | in-del | -/T | | | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014995 | GTCCTGAAGGACACG[-/T]ATGTCCAGGTGCGCC | 138151 |
rs55702496 | snp | A/C | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136066619 | TCCTACATGACCCAG[A/C]AATTCCAACCCTAGG | 138151 |
rs55705101 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | NACC2 | GRCh38.p7 | 9:136081095 | GGAGAAGAAACGCGC[A/G]TTTCCCATATTTCTC | 138151 |
rs55730735 | snp | A/C | 0.17654 | 0.238964 | intron-variant | NACC2 | GRCh38.p7 | 9:136063907 | AAAAAACAAAAAAAA[A/C]AAAAATCACTTAAAC | 138151 |
rs55737177 | snp | A/G | 0.185472 | 0.241529 | intron-variant | NACC2 | GRCh38.p7 | 9:136078954 | GCCCTTAGCACCGTC[A/G]CCGGCATGATGCCGC | 138151 |
rs55752144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136087037 | TGGACCCTAACATGC[A/G]TCCTTACAGAAGGGA | 138151 |
rs55772391 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078495 | AGAAATACCATTACC[C/T]TACTGTACAGATGAG | 138151 |
rs55789925 | snp | A/C | 0.375 | 0.216506 | intron-variant | NACC2 | GRCh38.p7 | 9:136063904 | AAAAAAAAACAAAAA[A/C]AACAAAAATCACTTA | 138151 |
rs55795218 | snp | A/G | 0.030278 | 0.119257 | intron-variant | NACC2 | GRCh38.p7 | 9:136067704 | GCCGAGCGTGGTGGC[A/G]GGCACCTGTAGTCCC | 138151 |
rs55818000 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | NACC2 | GRCh38.p7 | 9:136088414 | TGGATCCAAGCCACC[A/G]TCCACATCTTTCCCA | 138151 |
rs55876239 | snp | C/T | 0.0376258 | 0.131898 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013637 | TTCATTTTTCTGTTG[C/T]GGGGGTTGCATCCAC | 138151 |
rs55929946 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136089486 | TCCATGTCACCCCCC[A/C]CAACCCCACCTGGTG | 138151 |
rs55939904 | in-del | -/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009550 | AAAGCAACGTATTTT[-/T]CTGGAGGGCAGGCAT | 138151 |
rs56027452 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | NACC2 | GRCh38.p7 | 9:136072956 | ATATTTGTAGAATCC[A/G]GGGCTAGGCAGAGAG | 138151 |
rs56033139 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | NACC2 | GRCh38.p7 | 9:136081023 | GAGGTGATGGAGGAG[A/G]AAGTTTTCATCCCAG | 138151 |
rs56035900 | in-del | -/ATTC/ATTCATTCATTC | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031354 | TTCATTCATTCATTC[-/ATTC/ATTCATTCATTC]TGAGATAGAGTCTTG | 138151 |
rs56053365 | snp | C/T | 0.101301 | 0.200969 | intron-variant | NACC2 | GRCh38.p7 | 9:136083420 | TTTGGCCTTCACCCC[C/T]GTACTAGGAATAGCA | 138151 |
rs56085853 | snp | A/C | 0.0452528 | 0.143452 | intron-variant | NACC2 | GRCh38.p7 | 9:136076641 | CATGGGAATGTTCTT[A/C]CTGCCACTGAACTGT | 138151 |
rs56102761 | in-del | -/CA | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007466 | ACAGACGCACACACA[-/CA]GACGCACACACGCAC | 138151 |
rs56111648 | snp | A/G | 0.425432 | 0.178112 | intron-variant | NACC2 | GRCh38.p7 | 9:136066206 | TCAAAAAAAAAAAAA[A/G]AAAGAAAGAAAAAGA | 138151 |
rs56146602 | in-del | -/GACGCACATACA | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007557 | AGACACGCACACACA[-/GACGCACATACA]CACAGACACGCGCAC | 138151 |
rs56151742 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136063897 | CAAAAAAAAAAAAAA[-/A]CAAAAAAAACAAAAA | 138151 |
rs56162840 | in-del | -/CA | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007407 | AGAGACACGCACGTG[-/CA]CACACAGACGCGCGT | 138151 |
rs56188305 | in-del | -/CA | 0.466308 | 0.125343 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007456 | GCGCACACACACGCG[-/CA]CACAGACGCACACAC | 138151 |
rs56258735 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | NACC2 | GRCh38.p7 | 9:136089317 | TTCCTGAGGTCCCCA[C/T]GGCCCTAGGAGGGAG | 138151 |
rs56279831 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NACC2 | GRCh38.p7 | 9:136057841 | GGTTGTGGAAGCGGT[C/T]GGATCCCAGGCACCG | 138151 |
rs56335898 | in-del | -/ACACACAG/CA | 0 | 0 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007514 | ACAGACGCGCACACA[-/ACACACAG/CA]GACGCACAGACGTGC | 138151 |
rs56678073 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NACC2 | GRCh38.p7 | 9:136072955 | AATATTTGTAGAATC[C/T]GGGGCTAGGCAGAGA | 138151 |
rs56969554 | snp | C/T | 0.379354 | 0.213933 | intron-variant | NACC2 | GRCh38.p7 | 9:136068196 | CACTACATTTATCTT[C/T]TTTAAAAAAGTAATT | 138151 |
rs57189326 | snp | C/T | 0.040671 | 0.13668 | intron-variant | NACC2 | GRCh38.p7 | 9:136043169 | CTGGTCTTTGAGAGT[C/T]ACCATTACAATAATG | 138151 |
rs57193817 | snp | A/T | 0.367091 | 0.220884 | intron-variant | NACC2 | GRCh38.p7 | 9:136066948 | TCATTTAAAAAGATT[A/T]AAAAAAAAAAAAAAA | 138151 |
rs57318567 | snp | A/G | 0.472803 | 0.113397 | intron-variant | NACC2 | GRCh38.p7 | 9:136061065 | CTGGAACGGACGGAC[A/G]CCCCCTCAGTGGCTA | 138151 |
rs57460855 | in-del | -/TG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136033940 | GTGTGTGTGTGTGTG[-/TG]AGATATTTGGCAATC | 138151 |
rs57478602 | snp | A/G | 0.0391387 | 0.134304 | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016572 | AGGCCACTCTGTGCC[A/G]CTCTCCTGCTGGCCT | 138151 |
rs57617664 | snp | C/T | 0.112983 | 0.209108 | intron-variant | NACC2 | GRCh38.p7 | 9:136064211 | GGAGAATCACTTGAG[C/T]CCAGGCGATCGAGGC | 138151 |
rs57714320 | snp | A/G | 0.0807149 | 0.183963 | intron-variant | NACC2 | GRCh38.p7 | 9:136022626 | CCAGTGCTTCTGGCA[A/G]TGAGGGGGGCTCACC | 138151 |
rs57801994 | in-del | -/TGTG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136033938 | GTGTGTGTGTGTGTG[-/TGTG]AGATATTTGGCAATC | 138151 |
rs57990545 | in-del | -/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136079072 | CTTTTTTTTTTTTTT[-/T]AAGTGCACACGGTAT | 138151 |
rs58130370 | in-del | -/CCTACTAAACC | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136033481 | AACCCCTACTAAACC[-/CCTACTAAACC]TCTACTAAAAATACA | 138151 |
rs58132081 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067286 | AAAAAAAAAAAAAAA[-/A]TTGTTGTTGCCTAGA | 138151 |
rs58207305 | in-del | -/GA | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007396 | AGACACGCGTGCAGA[-/GA]CACGCACGTGCACAC | 138151 |
rs58299663 | snp | A/G | 0.150667 | 0.229419 | intron-variant | NACC2 | GRCh38.p7 | 9:136027013 | GCAGGGGGATCACCC[A/G]AGGTCAGGAGTTCAA | 138151 |
rs58484124 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136034870 | AGGCACTGGCGGGCC[C/G]ATCACCTGAGGTCAG | 138151 |
rs58499836 | in-del | -/GA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136042777 | ACACAGAGACACACA[-/GA]CACACACACACATAG | 138151 |
rs58509588 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | NACC2 | GRCh38.p7 | 9:136022536 | CCTTCCCTGCTGTTG[C/T]CCCTTCCACCCAGCT | 138151 |
rs58590758 | snp | A/G | 0.046775 | 0.145601 | intron-variant | NACC2 | GRCh38.p7 | 9:136069347 | TGAGGTCAGGAGGTC[A/G]AGACCAGCCTGGCCA | 138151 |
rs58765981 | in-del | -/CAGAGACA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136042863 | ACACACACAGAGACA[-/CAGAGACA]AACAGACACACACAC | 138151 |
rs58780352 | in-del | -/A/AA | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136068499 | AAAAAAAAAAAAAAA[-/A/AA]GTAATTGTGCAATGA | 138151 |
rs58787166 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136050674 | TCCCCCGCCGGGGGC[G/T]TACAAAGAGCGAGCC | 138151 |
rs58832474 | in-del | -/CA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136053894 | CAGGGCTGACACAGA[-/CA]GCAAGGGACAATGTA | 138151 |
rs58998041 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136041176 | CCTGTAATCCCAGCA[C/T]TTTGGAAGGCCAAGA | 138151 |
rs59062927 | snp | A/C | 0.112983 | 0.209108 | intron-variant | NACC2 | GRCh38.p7 | 9:136063211 | CAGGGATGAGCAGCT[A/C]CCGGGACCCCTGGGC | 138151 |
rs59105066 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NACC2 | GRCh38.p7 | 9:136086417 | TGGTCTGGATGGCAC[C/T]GGGCCTGGCTCTTGA | 138151 |
rs59205470 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | NACC2 | GRCh38.p7 | 9:136084742 | GCACACACACACATA[C/T]ATCACGCAGCCTGGA | 138151 |
rs59717576 | snp | C/T | 0.101658 | 0.201233 | intron-variant | NACC2 | GRCh38.p7 | 9:136083133 | CCTCGATGCCAGAAA[C/T]GGGGCCACCCTGCTG | 138151 |
rs59801729 | snp | C/G | 0.0295035 | 0.117819 | intron-variant | NACC2 | GRCh38.p7 | 9:136088662 | CCCCCACCCAGCCGG[C/G]CAGGAGGCATCGTGG | 138151 |
rs59820091 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136065817 | CCTGTCTCCAAAAAA[-/A]AAAAAAGAAAAGGAA | 138151 |
rs59908825 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | NACC2 | GRCh38.p7 | 9:136029317 | GAGCTGAGCAGATGT[C/T]GAGGAGACCTGCCTG | 138151 |
rs59998878 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136054767 | GTGAGATTCAACACA[C/G]TCATTCACTTATGGA | 138151 |
rs60013069 | in-del | -/ACACACAC | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096512 | CACACACACACACAC[-/ACACACAC]TTCACTCCCTGGCTT | 138151 |
rs60119969 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | NACC2 | GRCh38.p7 | 9:136075814 | TGGGCTCTGAGGCTC[A/G]GGACACAAGATTCAA | 138151 |
rs60257854 | snp | C/T | 0.144632 | 0.226711 | intron-variant | NACC2 | GRCh38.p7 | 9:136065004 | GACTGGATAGCCACA[C/T]GCAAAAGAATGAAGC | 138151 |
rs60290292 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | NACC2 | GRCh38.p7 | 9:136080812 | TGCAGGGAGAGCAGA[C/T]GGCAGATGACCACAG | 138151 |
rs60298224 | in-del | -/AC | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007451 | CAGACGCGCACACAC[-/AC]GCGCACACAGACGCA | 138151 |
rs60320127 | in-del | -/TGTGTGTGTGTGTG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136033928 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGTGTG]AGATATTTGGCAATC | 138151 |
rs60355850 | in-del | -/A | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136070680 | TCAGAAAAAAAAAAA[-/A]CAAAAACCAAAAACT | 138151 |
rs60426293 | snp | C/T | 0.0829062 | 0.185956 | intron-variant | NACC2 | GRCh38.p7 | 9:136088829 | GGCTGGGCTGTCCCA[C/T]AAAGGGACCTACCCC | 138151 |
rs60431955 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136035712 | AATGTCCTTGTTTGT[A/T]AAAAAAAAAAAAAAG | 138151 |
rs60459680 | snp | A/G | 0.132409 | 0.220618 | intron-variant | NACC2 | GRCh38.p7 | 9:136025514 | CAACTAGCAGACACC[A/G]AATTTAAAATAACAA | 138151 |
rs60463941 | in-del | -/T | 0.409041 | 0.192888 | intron-variant | NACC2 | GRCh38.p7 | 9:136058380 | GCCAGGGACCCGGGA[-/T]TTCCCATCCTCAGGG | 138151 |
rs60537556 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | NACC2 | GRCh38.p7 | 9:136019257 | ATGGCAGAGACAGGA[C/T]GGCTCATCCCTCGTG | 138151 |
rs60666107 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031551 | CTGTGTCGGCCAGGC[C/T]GGTCTCGAACTCCTG | 138151 |
rs60751608 | in-del | -/A | 0.420415 | 0.182917 | intron-variant | NACC2 | GRCh38.p7 | 9:136091832 | AGCAAGGATTTGCTT[-/A]AAAAAAAAAACCAAC | 138151 |
rs60843730 | snp | C/T | 0.105924 | 0.204309 | intron-variant | NACC2 | GRCh38.p7 | 9:136088783 | GGGCTCAGGCCTGGG[C/T]GTGGAGGGCGGGATG | 138151 |
rs60904172 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136033668 | AAAAAAAAAAAAAAA[-/A]GAACTTCTAGGAATA | 138151 |
rs60945683 | in-del | -/AG | 0.495483 | 0.0473088 | intron-variant | NACC2 | GRCh38.p7 | 9:136066205 | TCAAAAAAAAAAAAA[-/AG]GAAAGAAAGAAAAAG | 138151 |
rs61106331 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136040356 | TCTCAAAAAAAAAAA[-/A]TCAACTTTATTCCTA | 138151 |
rs61208098 | in-del | -/ATAA | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136072872 | TAAATAAATAAATAA[-/ATAA]CCCCAAAATGAATTG | 138151 |
rs61360488 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136066944 | CAGATCATTTAAAAA[G/T]ATTAAAAAAAAAAAA | 138151 |
rs61508838 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | NACC2 | GRCh38.p7 | 9:136033510 | CAAAAATTAGCCAGG[C/T]GTGGTGGCGGGTGCC | 138151 |
rs61742050 | snp | C/T | 0.032955 | 0.124062 | missense | NACC2 | GRCh38.p7 | 9:136011887 | TGACCGTGCGGTACA[C/T]CTCCACGCCCTCCGG | 138151 |
rs62583479 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | NACC2 | GRCh38.p7 | 9:136079485 | CTGTACAGGCTGGAC[A/G]CCAGCAGGTGGGGCA | 138151 |
rs62583482 | snp | A/C | 0.179105 | 0.239737 | intron-variant | NACC2 | GRCh38.p7 | 9:136080619 | CTACTGCCAGCACAC[A/C]ATCCCCCACCCCACA | 138151 |
rs62583484 | snp | C/T | 0.49263 | 0.0602539 | intron-variant | NACC2 | GRCh38.p7 | 9:136082664 | CTCCACGGACCTGCC[C/T]CCCAAGAAGCACCCC | 138151 |
rs62583485 | snp | A/G | 0.499866 | 0.0081858 | intron-variant | NACC2 | GRCh38.p7 | 9:136082669 | CGGACCTGCCTCCCA[A/G]GAAGCACCCCTCCTG | 138151 |
rs62583532 | snp | A/G | 0.397994 | 0.201489 | intron-variant | NACC2 | GRCh38.p7 | 9:136091824 | GCTGGTGAGAGCAAG[A/G]ATTTGCTTAAAAAAA | 138151 |
rs62585067 | snp | C/T | 0.0599851 | 0.162463 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007574 | ACAGACACGCGCACA[C/T]GCACACTCTCACCCA | 138151 |
rs62585076 | snp | C/T | 0.170733 | 0.237101 | intron-variant | NACC2 | GRCh38.p7 | 9:136019100 | ACACCCCGCCCCGAG[C/T]GGAAGCTCGTCCGCA | 138151 |
rs62989061 | snp | A/C | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136071546 | AGACTCCATCTCAAA[A/C]AAAAAAAAAAAAAAA | 138151 |
rs66778034 | snp | A/C | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136062172 | CAGGACAGGACAGGA[A/C]AGGAAAGGAAAGAGA | 138151 |
rs66834324 | in-del | -/AC | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096494 | AGCTCTGCGTCCAGA[-/AC]ACACACACACACACA | 138151 |
rs66977117 | in-del | -/GT/GTGC | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024249 | GTGTGAGGACAGAGG[-/GT/GTGC]GTGTGTGTGAGGACA | 138151 |
rs67068252 | in-del | -/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136073438 | GTCTCAAAAAAAAAA[-/T]TTTTAATAAAAAATA | 138151 |
rs67277453 | in-del | -/TGTGTGTGAGGACAGAGGGTGTGTGTGAGGACAGAGGG | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136024231 | TGTGAGGACAGAGGG[lengthTooLong]TGTGTGTGAGGACAG | 138151 |
rs67775385 | snp | C/G | 0.0494327 | 0.149241 | intron-variant | NACC2 | GRCh38.p7 | 9:136083359 | TTCCCAGGCTGGGTT[C/G]GGGGGGAGGCAGCCA | 138151 |
rs71384044 | in-del | -/TGGTACAGCTG | 0.368938 | 0.219895 | intron-variant | NACC2 | GRCh38.p7 | 9:136029712 | TGCTTGAGGTATGCC[-/TGGTACAGCTG]CAGCCCTGCAGGGAG | 138151 |
rs71384047 | in-del | -/T/TTT | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136068933 | CTTTTTTTTTTTTTT[-/T/TTT]AAAGATGGAGTTTTA | 138151 |
rs71492103 | in-del | -/A | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136093842 | GGCGGGGGCTGCCTG[-/A]ACCCTGACCTAACTC | 138151 |
rs71507095 | in-del | -/GTGTGT | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136024156 | GTGTGTGGGGACAGA[-/GTGTGT]GTGTGTGTGTGTGTG | 138151 |
rs71507097 | in-del | -/A | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136091833 | AGCAAGGATTTGCTT[-/A]AAAAAAAAACCAACA | 138151 |
rs71508836 | snp | C/T | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136069029 | CTCCTGCCTTAGCCT[C/T]CCAAGTAGCCAGGAT | 138151 |
rs71663452 | in-del | -/ACACACAG | 0.342806 | 0.232136 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007515 | CATGCACAGACGCGC[-/ACACACAG]ACGCACAGACGTGCA | 138151 |
rs71706881 | in-del | -/CA | 0.121717 | 0.214577 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007444 | ATACACACAGACGCG[-/CA]CACACACGCGCACAC | 138151 |
rs71709921 | in-del | -/CA | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007408 | GAGACACGCACGTGC[-/CA]ACACAGACGCGCGTG | 138151 |
rs71759303 | in-del | -/ACAC | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007431 | CGCGCGTGCACACAT[-/ACAC]ACAGACGCGCACACA | 138151 |
rs71922437 | in-del | -/AA/ACACACACACACACACAC | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096493 | AGCTCTGCGTCCAGA[-/AA/ACACACACACACACACAC]ACACACACACACACA | 138151 |
rs72168571 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136071543 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 138151 |
rs72275644 | in-del | -/ACAGG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136062126 | GCGAGACAGGACAGG[-/ACAGG]ACAGGACAGGACAGG | 138151 |
rs72413718 | in-del | -/AG | 0.105214 | 0.203807 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007393 | CACAGACACGCGTGC[-/AG]AGACACGCACGTGCA | 138151 |
rs72549966 | in-del | -/T | | | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014993 | ATGTCCTGAAGGACA[-/T]CGATGTCCAGGTGCG | 138151 |
rs72656977 | snp | G/T | 0.5 | 0 | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014061 | GGGGAGGGGGGGAGG[G/T]GGAGGGGGAGGAGGA | 138151 |
rs72656978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136018247 | AAACTCTACAGGGGT[A/G]GCTGAGCCTCGGGGC | 138151 |
rs72773707 | snp | C/G | 0.0471551 | 0.14613 | intron-variant | NACC2 | GRCh38.p7 | 9:136070076 | ACTTCAAGAACTTTA[C/G]AAGACTTAAAATTAC | 138151 |
rs72773710 | snp | C/G | 0.0471551 | 0.14613 | intron-variant | NACC2 | GRCh38.p7 | 9:136075628 | GGTCCTGCGGGAGCA[C/G]AGCCTGCAGGGCCCC | 138151 |
rs72773711 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | NACC2 | GRCh38.p7 | 9:136075754 | AGACCCACCCAACAC[C/T]CACAGGCCCTGTCGG | 138151 |
rs72773712 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | NACC2 | GRCh38.p7 | 9:136077493 | AGAGAAAAAACAAGC[C/T]GAGAAGGACAGACCT | 138151 |
rs72773713 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | NACC2 | GRCh38.p7 | 9:136078666 | CGGGACAGAAAGGGG[C/T]GTGGGAATGGCTGGG | 138151 |
rs72773715 | snp | G/T | 0.0444908 | 0.142359 | intron-variant | NACC2 | GRCh38.p7 | 9:136078854 | AGGGCAGGGCCTCTC[G/T]CCCCTTGTCCAGGCG | 138151 |
rs72773717 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | NACC2 | GRCh38.p7 | 9:136080301 | GAGCCCAGGCCCCTT[C/T]GCTGCCCCTACATGG | 138151 |
rs72773719 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | NACC2 | GRCh38.p7 | 9:136081016 | ATTAACAGAGGTGAT[A/G]GAGGAGGAAGTTTTC | 138151 |
rs72773720 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | NACC2 | GRCh38.p7 | 9:136081047 | ATCCCAGAACCCCAC[A/G]GGCCCAGGGTCACGG | 138151 |
rs72773721 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | NACC2 | GRCh38.p7 | 9:136081979 | CAGGGTGGAGCTGAC[A/G]CGAGAGCCAGGCTGC | 138151 |
rs72773723 | snp | C/T | 0.097727 | 0.198275 | intron-variant | NACC2 | GRCh38.p7 | 9:136082326 | CCCCAAGGCCAAGTC[C/T]GGGCTCTGCCCCGCC | 138151 |
rs72773725 | snp | C/T | 0.100944 | 0.200705 | intron-variant | NACC2 | GRCh38.p7 | 9:136083877 | ATCTTCTCAGACAGA[C/T]GATGTCCACCAAGAA | 138151 |
rs72773726 | snp | C/T | 0.101301 | 0.200969 | intron-variant | NACC2 | GRCh38.p7 | 9:136083957 | CTGAGAAAGCCTCTC[C/T]GCCTCACCCCAACTT | 138151 |
rs72773727 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | NACC2 | GRCh38.p7 | 9:136084441 | CAACGTCCAAGAAGG[C/T]GGTATCTCTGACGTC | 138151 |
rs72773728 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | NACC2 | GRCh38.p7 | 9:136084835 | AATGAGCCAGTCACA[C/T]GAGGACACCCCCTGT | 138151 |
rs72773729 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | NACC2 | GRCh38.p7 | 9:136086322 | CAGAGCTGGGAGGGG[C/T]TTGGGGGGTGGGGGT | 138151 |
rs72773730 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | NACC2 | GRCh38.p7 | 9:136086900 | ACTAAAGGCTTTCTG[C/T]CCCTCCCACACCACA | 138151 |
rs72773731 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | NACC2 | GRCh38.p7 | 9:136087476 | AGAGCGGCATTCGCA[A/G]GGGTCGGGCCAGCCC | 138151 |
rs72773735 | snp | C/G | 0.0562307 | 0.157967 | intron-variant | NACC2 | GRCh38.p7 | 9:136091691 | AGCAAACGCAGGAAG[C/G]CCACAGCTGAGGGAG | 138151 |
rs72773737 | snp | A/T | 0.0463947 | 0.145069 | intron-variant | NACC2 | GRCh38.p7 | 9:136093685 | GGACTCTGGCCCAGC[A/T]ACCACCCAACAGTGA | 138151 |
rs72773739 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096216 | GGTCCTTGCAGGAGA[A/G]TGGAGTGATACCGCC | 138151 |
rs73551123 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NACC2 | GRCh38.p7 | 9:136017367 | GAGCCCCTCTAGAGC[A/G]TTCATGGAGGGCCAG | 138151 |
rs73551126 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | NACC2 | GRCh38.p7 | 9:136020761 | GACAGACAGGTCAAT[A/G]GCACAGAATAGGAGA | 138151 |
rs73551132 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | NACC2 | GRCh38.p7 | 9:136022938 | GTTAAGACACAGCCC[A/G]TTTCGTGGATGCTGA | 138151 |
rs73551133 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | NACC2 | GRCh38.p7 | 9:136022957 | CGTGGATGCTGACAC[A/G]TGGGGAAATGCAGAA | 138151 |
rs73551135 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | NACC2 | GRCh38.p7 | 9:136023896 | ACGGGATGCCACCCA[C/T]ACAAGTGTGTACCCA | 138151 |
rs73551137 | snp | C/G | 0.079617 | 0.182947 | intron-variant | NACC2 | GRCh38.p7 | 9:136024277 | ACAGAGGGTGTGTGT[C/G]AGGACAGAGGGTGCG | 138151 |
rs73551148 | snp | C/T | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136031342 | ATTCATTCATTCATT[C/T]ATTCATTCATTCTGA | 138151 |
rs73551172 | snp | C/T | 0.112983 | 0.209108 | intron-variant | NACC2 | GRCh38.p7 | 9:136065302 | CCAGCCTCGGCAACA[C/T]AGTGGGACCTCGTAT | 138151 |
rs73552954 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | NACC2 | GRCh38.p7 | 9:136075187 | AGGCTGCAACGCCCC[C/T]CACACACAGACTTGG | 138151 |
rs73552962 | snp | G/T | 0.0352966 | 0.128072 | intron-variant | NACC2 | GRCh38.p7 | 9:136077772 | GGGGCAACAAAATTG[G/T]GCTTAAAATTATTTA | 138151 |
rs73552968 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | NACC2 | GRCh38.p7 | 9:136080232 | CTGCACCCCCAGCCT[A/G]TACAGCCTCATCCCA | 138151 |
rs73552971 | snp | A/G | 0.031825 | 0.122064 | intron-variant | NACC2 | GRCh38.p7 | 9:136080505 | TCAACCTGGGAGGCA[A/G]AGGTTGTGTGCTGAG | 138151 |
rs73552988 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | NACC2 | GRCh38.p7 | 9:136085047 | TTCCACTGAAAAAGC[C/T]AAAACGGTAAATTTT | 138151 |
rs73554858 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NACC2 | GRCh38.p7 | 9:136088790 | GGCCTGGGCGTGGAG[A/G]GCGGGATGGGCAGAA | 138151 |
rs73554868 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | NACC2 | GRCh38.p7 | 9:136092891 | ACCCACTGCGTGACC[C/G]TGCAAAGGGGATGGA | 138151 |
rs73554872 | snp | A/G | 0.0256215 | 0.110247 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136097105 | GCACCTTTTAAAGCA[A/G]ACCCTGCATCCCTAC | 138151 |
rs73568816 | snp | C/T | 0.0667028 | 0.170006 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010462 | ACCCGGGACCCCCTT[C/T]TTCCCCCAGTGGGAG | 138151 |
rs73568818 | snp | C/T | 0.0803491 | 0.183626 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010985 | CACAGGTGGAAGGCC[C/T]GGTGGGCCTGGCCCC | 138151 |
rs73568821 | snp | C/T | 0.0146672 | 0.084371 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012310 | AGGCCTGTTTTTAAT[C/T]TCTCCGGGCTTCCGT | 138151 |
rs73668053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015477 | CTGGCAGCTGGAAGG[C/T]GAGGCCAGCCCAGGC | 138151 |
rs73668054 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136057341 | ACTGTCAACAGGGAT[A/G]GCTCAGAGGAAGAGA | 138151 |
rs73668055 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | NACC2 | GRCh38.p7 | 9:136058479 | CATATTTTACCCTCT[A/G]GACATTCCTGTCTGG | 138151 |
rs73668056 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | NACC2 | GRCh38.p7 | 9:136060433 | CAACTTCTACAGCTC[A/G]GGAATGGCAACTGTG | 138151 |
rs73668057 | snp | A/G | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136060713 | TCCCAGGTGAAGAGC[A/G]TGAGAAACATAGCCG | 138151 |
rs73668058 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NACC2 | GRCh38.p7 | 9:136061389 | TAGAGGGGTCCCCTC[C/T]CTCCAGGCCCAGATG | 138151 |
rs73668059 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NACC2 | GRCh38.p7 | 9:136062330 | ACCTGCCATCTACCC[A/G]GACCCTGGAAAGTTA | 138151 |
rs73668060 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NACC2 | GRCh38.p7 | 9:136062434 | AGTGAGGTTTTGGCC[C/T]GTGGGGCATTAACCA | 138151 |
rs73668061 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | NACC2 | GRCh38.p7 | 9:136063175 | GTGGTTTGAGCCGCA[A/T]TCCCATTACGTGGCG | 138151 |
rs73668069 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | NACC2 | GRCh38.p7 | 9:136086574 | GGCTCCACTGTGACC[C/T]ACACGCTGTCATTTC | 138151 |
rs73668070 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | NACC2 | GRCh38.p7 | 9:136087653 | ACCCCATTCGGAGCT[C/T]ACAGCGGGAAAACTG | 138151 |
rs73668071 | snp | A/G | 0.029116 | 0.117091 | intron-variant | NACC2 | GRCh38.p7 | 9:136087659 | TTCGGAGCTCACAGC[A/G]GGAAAACTGAGACCC | 138151 |
rs73668072 | snp | C/T | 0.111224 | 0.207945 | intron-variant | NACC2 | GRCh38.p7 | 9:136088208 | GTGCTCTGTCCGGCT[C/T]CCTTCCAGTGGGACG | 138151 |
rs73668073 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | NACC2 | GRCh38.p7 | 9:136089562 | AAGAAGGTGAACCCA[C/G]CCTCGGGGTGCCCTC | 138151 |
rs73668074 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | NACC2 | GRCh38.p7 | 9:136093615 | TCCAAGTGGCTTTGC[C/T]GAAAGGACAGGGGGC | 138151 |
rs74312194 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NACC2 | GRCh38.p7 | 9:136061833 | GGCCATTACGAAAAG[C/T]TGGTGGCCGGGCGCG | 138151 |
rs74344950 | snp | A/C | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136087190 | GGCATGTGACAAAGT[A/C]TCCCTCAAAGCCTCT | 138151 |
rs74362000 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | NACC2 | GRCh38.p7 | 9:136076731 | TAAAAAATGTATTGG[C/T]CTGGTGGTGGCTCAT | 138151 |
rs74432124 | snp | A/C | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136060387 | AAGGTAATTACCGAT[A/C]TGAAAAATAAAGACC | 138151 |
rs74443815 | snp | A/G | 0.304688 | 0.243945 | intron-variant | NACC2 | GRCh38.p7 | 9:136094520 | GTTTCTTAGAGAAGG[A/G]GCTGGGGCCCCCCGA | 138151 |
rs74443985 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | NACC2 | GRCh38.p7 | 9:136074817 | GCGGGGCTCGGGGAT[A/G]TATCACTCAGCCTCG | 138151 |
rs74480615 | snp | A/G | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136075738 | CTGCGCCCAGGGGAG[A/G]AGACCCACCCAACAC | 138151 |
rs74653792 | snp | A/C | 0.040671 | 0.13668 | intron-variant | NACC2 | GRCh38.p7 | 9:136059910 | AGCCAAGACCCACCC[A/C]GATGTCCTGACCAGC | 138151 |
rs74688457 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136023417 | CTTCTCGACCAGCTC[A/T]ACAGTCCCATCAAAC | 138151 |
rs74690390 | snp | C/T | 0.118235 | 0.212457 | intron-variant | NACC2 | GRCh38.p7 | 9:136081046 | CATCCCAGAACCCCA[C/T]GGGCCCAGGGTCACG | 138151 |
rs74745514 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | NACC2 | GRCh38.p7 | 9:136061806 | CAGGTACAATGGCCC[A/G]GGTACAGAGCAGGCC | 138151 |
rs74893449 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | NACC2 | GRCh38.p7 | 9:136078869 | GCCCCTTGTCCAGGC[A/G]ACCTTGTGGGTAAGC | 138151 |
rs74900143 | snp | A/T | 0.375598 | 0.21616 | intron-variant | NACC2 | GRCh38.p7 | 9:136024407 | GGTGTGTGAGGACAG[A/T]GTGTGTGTGTGTGAG | 138151 |
rs74915977 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136032542 | TAAGAAGTTCTGGCC[A/C]GTTCAATGAGGCAAG | 138151 |
rs74924858 | snp | G/T | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136097227 | TTTTTTTTTTTTTTT[G/T]AGTCCGAGTCTCACA | 138151 |
rs74975533 | snp | A/C | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136056346 | AGGAACTCCCCCCAA[A/C]CCCGAGGCCCCCACA | 138151 |
rs75186387 | snp | A/C | 0.0240643 | 0.107019 | intron-variant | NACC2 | GRCh38.p7 | 9:136065722 | GAGGTGTGAGAATCA[A/C]TTTAACCTAGGAGGT | 138151 |
rs75219704 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NACC2 | GRCh38.p7 | 9:136056253 | AGAGCTGGGCTGCCC[A/G]GAGGCCTGGCTGCTA | 138151 |
rs75319824 | snp | A/C | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136064289 | GTGAGGCCCTGCCTC[A/C]AAAAAAAGACAAAAG | 138151 |
rs75369019 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136089915 | TCAAAAGTTGTGTGA[C/T]ACGGATTTCATTAAC | 138151 |
rs75386418 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | NACC2 | GRCh38.p7 | 9:136082103 | TCTCCACCTGAACAC[A/G]ACCTGCCGGGGCCCT | 138151 |
rs75389515 | snp | C/T | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136089368 | CACAGCCACCCCCCT[C/T]GCTAGAAACCTAGCA | 138151 |
rs75391192 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136097135 | CTGAATTCCAGGCCC[G/T]TGCTACTGAGTATGT | 138151 |
rs75536718 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | NACC2 | GRCh38.p7 | 9:136017314 | CCATGGTGCCACCCC[A/G]AGGTCCCTGGGCAGG | 138151 |
rs75596264 | snp | A/C | 0.208169 | 0.246476 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096493 | CAGCTCTGCGTCCAG[A/C]ACACACACACACACA | 138151 |
rs75640440 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136027548 | GAAATTTAATTCAGA[A/G]TTCATAACAAAAAAG | 138151 |
rs75905441 | snp | A/T | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136074303 | ATAAAATACAAAAAA[A/T]TTAGCCGGGCATGGT | 138151 |
rs75908384 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | NACC2 | GRCh38.p7 | 9:136022767 | AGAAACGACTTCCAC[A/G]CTGTACTTGGTGGGA | 138151 |
rs75956170 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | NACC2 | GRCh38.p7 | 9:136029608 | AGGAGGTCCGTGAGC[C/T]GGGGCTGTGACACCT | 138151 |
rs75959523 | snp | A/C | 0.407502 | 0.194147 | intron-variant | NACC2 | GRCh38.p7 | 9:136094743 | CCGGGAGGGGTGGGT[A/C]CCTCCGCCCTGGCCC | 138151 |
rs75969216 | snp | A/G | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136025021 | GATGGAGCAAAATCA[A/G]CTGCCAAGAAACGAA | 138151 |
rs76082936 | snp | C/T | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136089772 | TATTTTCTTAAAAGC[C/T]TTTTTTTTTTCTTTT | 138151 |
rs76096877 | snp | C/T | 0.0858192 | 0.188533 | intron-variant | NACC2 | GRCh38.p7 | 9:136090047 | AAAATTTAACAAAGG[C/T]GCTTAGCTGTGCAAT | 138151 |
rs76145142 | snp | A/T | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136066946 | GATCATTTAAAAAGA[A/T]TAAAAAAAAAAAAAA | 138151 |
rs76205308 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | NACC2 | GRCh38.p7 | 9:136057515 | AAGGTTTCCAAAGAA[C/T]TAAGCTGTGTTTCGA | 138151 |
rs76213437 | snp | A/G | 0.132751 | 0.2208 | intron-variant | NACC2 | GRCh38.p7 | 9:136024200 | GAGTGTGTGTGTGTG[A/G]GGACAGAGTGTGTGT | 138151 |
rs76353438 | snp | A/G | 0.030278 | 0.119257 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009368 | GCTCCCTCTAGGCTG[A/G]GTGGTTCTTAGTTCA | 138151 |
rs76384747 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | NACC2 | GRCh38.p7 | 9:136080088 | CAGAGACACACAGTC[C/T]CTACCCCGGGCGTGG | 138151 |
rs76386759 | snp | C/G | 0.0437281 | 0.141251 | intron-variant | NACC2 | GRCh38.p7 | 9:136061258 | GACACCCCAGCTGGA[C/G]TGGTCACCAAACCCA | 138151 |
rs76429456 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | NACC2 | GRCh38.p7 | 9:136083692 | GCAGGCGGGGGCCCC[A/G]AGACACTGTGGCCTG | 138151 |
rs76446261 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024066 | ACAGCGTGTGTGTGT[A/G]AGGCCAGAGTGTGAG | 138151 |
rs76465012 | snp | C/G | 0.0670745 | 0.170406 | intron-variant | NACC2 | GRCh38.p7 | 9:136078352 | GGACAGGCACATCTG[C/G]GGGCAGGTTCTCCAA | 138151 |
rs76516475 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | NACC2 | GRCh38.p7 | 9:136094007 | CGACCTGGAGGGACA[C/G]GGACTCTGGCAGGAG | 138151 |
rs76537856 | snp | A/G | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136030787 | CCATCTCAGCCTCCC[A/G]AGTAGCTGGGACCTC | 138151 |
rs76622527 | snp | A/G | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136023135 | AGGAGGGAGGGAGGA[A/G]GGACCTGTACGCATA | 138151 |
rs76628624 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | NACC2 | GRCh38.p7 | 9:136059281 | ACACGCACAGGGGCC[C/T]GCAGAGCTAAGCAAG | 138151 |
rs76632018 | snp | A/G | 0.116838 | 0.211584 | intron-variant | NACC2 | GRCh38.p7 | 9:136086075 | CAGGGCAGCTCCGAC[A/G]GGCAGGAGCCGCCTC | 138151 |
rs76763287 | snp | C/T | 0.0333695 | 0.124785 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012481 | AGCCCAGGCCAAGGC[C/T]GGGTCATTCCTCCCA | 138151 |
rs76807903 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NACC2 | GRCh38.p7 | 9:136080207 | CACCAGGGATGGTGC[C/T]AGAGCGGTACTGCAC | 138151 |
rs76913198 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | NACC2 | GRCh38.p7 | 9:136075675 | TGATGCTGTCCTGAG[C/T]TCCCTGTGCCCGGTC | 138151 |
rs77006359 | snp | C/G | 0.0667028 | 0.170006 | intron-variant | NACC2 | GRCh38.p7 | 9:136079733 | AAGCCAGATGGGTCT[C/G]AGGCCTCCCACTACC | 138151 |
rs77040220 | snp | C/T | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136085778 | ATCTTTTACCTTTTT[C/T]CTTAAACATCTGAAG | 138151 |
rs77087194 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136018599 | GGGAGCTTCCCAAGG[C/G]CCAGGGACACCCAAG | 138151 |
rs77095802 | snp | C/T | 0.0759472 | 0.179459 | intron-variant | NACC2 | GRCh38.p7 | 9:136091682 | ACCGTAAACAGCAAA[C/T]GCAGGAAGGCCACAG | 138151 |
rs77109164 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | NACC2 | GRCh38.p7 | 9:136026940 | CCAGTAGAAAATAAC[A/G]TTTGTTGGCCGGGTG | 138151 |
rs77129267 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | NACC2 | GRCh38.p7 | 9:136085939 | GGGCTGGCAGAGCCC[A/G]GAGGCTGGGCACTGC | 138151 |
rs77185897 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NACC2 | GRCh38.p7 | 9:136066355 | GGCATCTGAAAAGGT[A/G]TTTCTCCAAATACTA | 138151 |
rs77198708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136027575 | AAAGATGACCAGAAA[A/G]TCCAAAAAGGTTTGT | 138151 |
rs77268538 | snp | A/G | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136030755 | CAACCTGCGCCTCCC[A/G]GGTTCAAGCGATCCT | 138151 |
rs77350949 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136069118 | TCGCCATGTTTACCA[G/T]GTTGGTCTCTAACTC | 138151 |
rs77387780 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NACC2 | GRCh38.p7 | 9:136063502 | AGTTCTCTGCATGTC[C/T]ATCACCAGGACCAGG | 138151 |
rs77393854 | snp | A/C | 0.0444908 | 0.142359 | intron-variant | NACC2 | GRCh38.p7 | 9:136075497 | CCTGCCGTCTCCTAC[A/C]TCGCGGTACAGTTTC | 138151 |
rs77423920 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | NACC2 | GRCh38.p7 | 9:136061700 | GAAAGAGGCAGATCG[A/G]AGGTCTAGCAGGCTC | 138151 |
rs77618929 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136063642 | TAATCCCAGCACTTG[A/G]GAGGCCAAGGCGGGT | 138151 |
rs77731760 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136094020 | CACGGACTCTGGCAG[A/G]AGAGTGCGGCCGCGC | 138151 |
rs77769653 | snp | C/T | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136074266 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 138151 |
rs77863522 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136066394 | TGTCCAATATACACA[C/T]GCAAAAATACTCAGC | 138151 |
rs77882719 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | NACC2 | GRCh38.p7 | 9:136017706 | CCAGCACAGCCACCC[C/T]GCTCAGGTGAGGGCG | 138151 |
rs78000312 | snp | A/C | 0.0539704 | 0.155153 | intron-variant | NACC2 | GRCh38.p7 | 9:136079347 | GAACGGGGTGCCATC[A/C]TCTGGCTTCCAGGCA | 138151 |
rs78012349 | snp | A/G | 0.102014 | 0.201495 | intron-variant | NACC2 | GRCh38.p7 | 9:136061057 | GTCACATACTGGAAC[A/G]GACGGACGCCCCCTC | 138151 |
rs78045426 | snp | A/G | 0.030278 | 0.119257 | intron-variant | NACC2 | GRCh38.p7 | 9:136094321 | CCTTCAGACCCACAG[A/G]TTTAAGCGGCTCCAC | 138151 |
rs78149338 | snp | C/T | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136074409 | AGTGAGCCGAGGTTG[C/T]GCCACTGCACTCCAG | 138151 |
rs78151781 | snp | A/C | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136025628 | TTAAAAAAAAAAAAA[A/C]CGCAGCCGGGCGCAG | 138151 |
rs78163854 | snp | A/C/T | 0.0166424 | 0.0896896 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014927 | ACCCTCTGGGAACAA[A/C/T]GGGGAGGGAATGCTT | 138151 |
rs78238245 | snp | A/C | 0.0411519 | 0.137414 | missense | NACC2 | GRCh38.p7 | 9:136011677 | GGATGACCGAGCCAG[A/C]CCCGTCCACCTCCTC | 138151 |
rs78251394 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | NACC2 | GRCh38.p7 | 9:136071661 | GACAATTTTGAGAGA[G/T]AATTAAGTGGGAGAA | 138151 |
rs78282156 | snp | C/T | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136077655 | ACAGAGGAGAAGGTC[C/T]CCAGGCGGTGACACC | 138151 |
rs78307828 | snp | C/T | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136030754 | ACAACCTGCGCCTCC[C/T]AGGTTCAAGCGATCC | 138151 |
rs78334615 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | NACC2 | GRCh38.p7 | 9:136087830 | AACGAGGCCCCAAGC[G/T]CCCTGTCCTCCCCGG | 138151 |
rs78345272 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | NACC2 | GRCh38.p7 | 9:136084938 | TGGGGCAAGGATGGG[G/T]AGTTTGTGTCTAATG | 138151 |
rs78557910 | snp | G/T | 0.0463947 | 0.145069 | intron-variant | NACC2 | GRCh38.p7 | 9:136077672 | CAGGCGGTGACACCT[G/T]AGCAGGGGGCAGCTG | 138151 |
rs78686109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136063498 | TGCAAGTTCTCTGCA[C/T]GTCCATCACCAGGAC | 138151 |
rs78706561 | snp | C/T | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136074407 | GCAGTGAGCCGAGGT[C/T]GTGCCACTGCACTCC | 138151 |
rs78732787 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136022090 | AGGCTGACCTGGCAC[A/T]TGCCCTGCACTATCT | 138151 |
rs78750824 | snp | C/T | 0.238749 | 0.249747 | intron-variant | NACC2 | GRCh38.p7 | 9:136019300 | GCCATTCAGAGGCCC[C/T]GTGAGTCGGGGCCAG | 138151 |
rs78859699 | snp | A/C | 0.0479149 | 0.147179 | intron-variant | NACC2 | GRCh38.p7 | 9:136029228 | GAAGGCCATAAAAAC[A/C]CCAGACTCAGCCAGA | 138151 |
rs78892281 | snp | A/G | 0.0792508 | 0.182605 | intron-variant | NACC2 | GRCh38.p7 | 9:136089163 | GAGAACCAGCGGGGC[A/G]GCAGCCACAGGCTAC | 138151 |
rs78938811 | snp | G/T | 0.0372196 | 0.131242 | intron-variant | NACC2 | GRCh38.p7 | 9:136060198 | TAATTGTCCTCGTGC[G/T]CCAGTGTGAGAATCT | 138151 |
rs78957971 | snp | C/T | 0.0337553 | 0.125452 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015834 | AGGTAAATTCCTGAG[C/T]GAGGCCCGGCCCCCA | 138151 |
rs78985728 | snp | A/G | 0.498369 | 0.0285077 | intron-variant | NACC2 | GRCh38.p7 | 9:136024370 | GTGTGTGAGGACAGA[A/G]GGTGTGTGTGTGAGG | 138151 |
rs79020547 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136089916 | CAAAAGTTGTGTGAT[A/C]CGGATTTCATTAACA | 138151 |
rs79105125 | snp | C/T | 0.416055 | 0.186885 | intron-variant | NACC2 | GRCh38.p7 | 9:136079374 | GGCAGGAGACACTCC[C/T]ACAAGCACAGGATGC | 138151 |
rs79106207 | snp | C/G | 0.0539704 | 0.155153 | intron-variant | NACC2 | GRCh38.p7 | 9:136074926 | GCGGGAATGGGTTCT[C/G]GCACGGCCTCCTTCT | 138151 |
rs79175912 | snp | A/G | 0.0531888 | 0.15416 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011699 | CACCTCCTCGCCGGC[A/G]TCGAAGGCGGGGTTG | 138151 |
rs79248116 | snp | A/G | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136024503 | GTGTGTGAGGACAGA[A/G]TGTGTGTGTGTGTGT | 138151 |
rs79306851 | snp | A/G | 0.029116 | 0.117091 | intron-variant | NACC2 | GRCh38.p7 | 9:136059856 | AGTCCCTACCTCGCC[A/G]TCAAAAGGACCCCAA | 138151 |
rs79335843 | snp | A/G | 0.0770498 | 0.180522 | intron-variant | NACC2 | GRCh38.p7 | 9:136075526 | TCTCAAACAGATCGC[A/G]CAGCTGGGGCCAAGC | 138151 |
rs79358346 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | NACC2 | GRCh38.p7 | 9:136059168 | TTAGCTGGGACATCT[A/G]GGGGCAAAACTGCCA | 138151 |
rs79410157 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136082665 | CCACGGACCTGCCTC[-/A]CCAAGAAGCACCCCT | 138151 |
rs79494322 | snp | A/T | 0.5 | 0 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007529 | CACACACAGACGCAC[A/T]GACGTGCACACACAG | 138151 |
rs79498013 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007535 | CAGACGCACAGACGT[A/G]CACACACAGACACGC | 138151 |
rs79557243 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | NACC2 | GRCh38.p7 | 9:136018795 | GTGGTATTTTAAAAC[A/G]TAATTACACACCCCC | 138151 |
rs79563230 | snp | A/G | 0.00636936 | 0.0560724 | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006471 | CCACCCCTGCCTTCA[A/G]TAGCCCAAGCTTGGC | 138151 |
rs79577435 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NACC2 | GRCh38.p7 | 9:136084641 | AGACGCGCACGCCAC[A/G]TCCATAGCGGCAGCA | 138151 |
rs79639146 | snp | A/C | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136089054 | AAAGGTGTTGCAAAA[A/C]CACACAGACACGAAA | 138151 |
rs79653069 | snp | C/T | 0.280256 | 0.248162 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010144 | CAGCCTCAAACCAAA[C/T]AGCCCCATCTTCCAT | 138151 |
rs79654328 | snp | G/T | 0.0279526 | 0.114869 | intron-variant | NACC2 | GRCh38.p7 | 9:136031222 | TAATTCTCAATTCAT[G/T]TAATGAGGCCAGATA | 138151 |
rs79659145 | snp | A/G | 0.0858192 | 0.188533 | intron-variant | NACC2 | GRCh38.p7 | 9:136089408 | GCCTGACTTCCAGGC[A/G]AAGGGTAGGGGGTAC | 138151 |
rs79695129 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136077190 | ACAAAAATTAGCTGG[C/G]CGTGGTGGCGGGCGC | 138151 |
rs79696449 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136063622 | AGCACGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 138151 |
rs79764491 | snp | A/G | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096491 | TTCAGCTCTGCGTCC[A/G]GAACACACACACACA | 138151 |
rs79804304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136080845 | CGGCCTGTGCCCGGC[A/G]CAAACTCCAGCCAGC | 138151 |
rs79872970 | snp | C/G | 0.0524604 | 0.153226 | intron-variant | NACC2 | GRCh38.p7 | 9:136089485 | CTCCATGTCACCCCC[C/G]ACAACCCCACCTGGT | 138151 |
rs79926189 | snp | A/T | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136025615 | GGATTAAGTCCTATT[A/T]AAAAAAAAAAAAACG | 138151 |
rs80055556 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | NACC2 | GRCh38.p7 | 9:136074314 | AAAAATTAGCCGGGC[A/G]TGGTGGTGGGCGCCT | 138151 |
rs80075748 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | NACC2 | GRCh38.p7 | 9:136091999 | CAGTCACATCTCCTC[C/T]GTGACTCTGGACAGG | 138151 |
rs80095305 | snp | A/C | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136069114 | TCAAGACCAGCCTGG[A/C]CAACATGGTGAAACC | 138151 |
rs80154253 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NACC2 | GRCh38.p7 | 9:136058459 | TCCCCAGGGCCCTGG[C/T]CATCCATATTTTACC | 138151 |
rs80231595 | snp | A/C | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136071542 | AGTGAGACTCCATCT[A/C]AAAAAAAAAAAAAAA | 138151 |
rs80260282 | snp | A/G | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136074405 | TTGCAGTGAGCCGAG[A/G]TTGTGCCACTGCACT | 138151 |
rs80337119 | snp | A/G | 0.0991586 | 0.199366 | intron-variant | NACC2 | GRCh38.p7 | 9:136091953 | GTAACCTCGCTCCCC[A/G]GCCCCCACAGCCAAG | 138151 |
rs111306879 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016580 | CTGTGCCGCTCTCCT[G/T]CTGGCCTGGGTCAGA | 138151 |
rs111384865 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136036036 | ATAAACTTCACTATA[A/T]AAAATTATATTAACA | 138151 |
rs111385168 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136040076 | TCCAGCTGGGCACAG[G/T]GGCTCACTCCTGTAA | 138151 |
rs111403208 | snp | A/T | 0.144632 | 0.226711 | intron-variant | NACC2 | GRCh38.p7 | 9:136063048 | ACTTTGCCGTCACTG[A/T]TTTCTTCTAATTTTT | 138151 |
rs111423151 | snp | C/T | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136016674 | GGAAGCTCTTGTGAA[C/T]GAGTGAGCAGAAGAT | 138151 |
rs111425367 | snp | C/T | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136030886 | CAGGCTGGTCTTAAA[C/T]TCCCAAGTTCAAGTG | 138151 |
rs111471024 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NACC2 | GRCh38.p7 | 9:136087402 | CTGGCCTGTCACCTG[C/T]ACAGCTGCAAATAGA | 138151 |
rs111498238 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136056361 | CCCCGAGGCCCCCAC[A/G]AAAGCCAGGATGGCG | 138151 |
rs111510851 | snp | C/G | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136024427 | GTGTGTGTGAGGACA[C/G]AGTGTGTGTGTGTGA | 138151 |
rs111529898 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136041197 | AAGGCCAAGACAGGC[A/G]GATCACTTGAGGTCA | 138151 |
rs111577093 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012657 | GCCTCACAAGGTTTT[G/T]TTTTTTTTTTTTTTT | 138151 |
rs111590353 | in-del | -/AAAT | 0.500314 | 0.0437912 | intron-variant | NACC2 | GRCh38.p7 | 9:136072850 | GTGAAACTCCGTCTC[-/AAAT]AAATAAATAAATAAA | 138151 |
rs111601271 | snp | G/T | 0.0825414 | 0.185628 | intron-variant | NACC2 | GRCh38.p7 | 9:136026206 | ATTAGCCAGGTGTGG[G/T]GGTGCGCACCTGTAA | 138151 |
rs111608425 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067284 | AAAAAAAAAAAAAAA[A/C]AATTGTTGTTGCCTA | 138151 |
rs111640894 | snp | G/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008016 | GAGGCCAGGCAGCCG[G/T]CTCCTATGTTCTAGG | 138151 |
rs111749974 | snp | C/G | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136028760 | GGGAAGCCCCCCTGC[C/G]TGCACAGGCTCAGAA | 138151 |
rs111780094 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | NACC2 | GRCh38.p7 | 9:136017072 | CTGTGCTGGCCTGAC[A/G]AGGAGCAACTCCATA | 138151 |
rs111782876 | snp | A/G | 0.015052 | 0.0854368 | synonymous-codon, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013248 | CTTCCGGCTGGGGTC[A/G]CTGGTGGACGAGCGG | 138151 |
rs111824453 | snp | C/T | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136067565 | TCGATGGGCCGGGCG[C/T]GGTGGCTCACGCCTG | 138151 |
rs111852401 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136084442 | AACGTCCAAGAAGGC[A/G]GTATCTCTGACGTCC | 138151 |
rs111909442 | snp | G/T | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136066536 | AGAGATGTAGCGATC[G/T]GGAATGCAAAATGTT | 138151 |
rs111923676 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | NACC2 | GRCh38.p7 | 9:136074007 | CTTGACTATTTTTTT[A/T]AAAAAATTAAGATCT | 138151 |
rs111932824 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015869 | CTTCTGGACTCGGAC[A/G]TGTTTGTTCTGCCAG | 138151 |
rs111966498 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | NACC2 | GRCh38.p7 | 9:136089355 | GGCTCCCCCTCCCCA[C/T]AGCCACCCCCCTTGC | 138151 |
rs112012143 | snp | A/C | 0.021333 | 0.101051 | intron-variant | NACC2 | GRCh38.p7 | 9:136066080 | TGCCTGTAACCCCAG[A/C]TACTCGGGAGGCTGA | 138151 |
rs112037548 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136039604 | AGTTGAATCTAGCAA[C/T]ATATGTAAACACTGT | 138151 |
rs112071544 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | NACC2 | GRCh38.p7 | 9:136077165 | GCCTGGGTGACAGAG[A/G]AAAAAACAAACAAAA | 138151 |
rs112125936 | in-del | -/TC | 0.394354 | 0.204112 | intron-variant | NACC2 | GRCh38.p7 | 9:136064394 | AAAATCACAAGTATT[-/TC]TCTCTACACTTGCAA | 138151 |
rs112168981 | snp | C/T | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136077825 | AAGTAGTTTGAAAAG[C/T]GAATAAGGAATCAGT | 138151 |
rs112176367 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136046762 | CGGGTGGTGACGCGG[G/T]ACCTGGAGGGAGGGA | 138151 |
rs112191177 | snp | C/T | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136077218 | CGCCTGTAGTCCCAG[C/T]CACTTGGGAGGCTGA | 138151 |
rs112256215 | snp | C/T | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136064043 | CCTATAATCCCAGCA[C/T]TTTGGGAGGTCAAGG | 138151 |
rs112337563 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | NACC2 | GRCh38.p7 | 9:136067060 | GTTCGAGACCAGCCT[C/T]GGCAAGCAACATGTC | 138151 |
rs112379752 | in-del | -/C | 0.00557542 | 0.0525036 | intron-variant | NACC2 | GRCh38.p7 | 9:136021609 | ACTTCTAGGTATTTG[-/C]CCAAGAAAAATGGGA | 138151 |
rs112400539 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136061885 | AGCACTTTGGGAGGC[C/G]AAGGCGGGCGGATCA | 138151 |
rs112413089 | snp | C/T | 0.0490535 | 0.14873 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009859 | GGGGGTGCTGATGGG[C/T]GCAGGGCTGCACTTG | 138151 |
rs112433274 | snp | A/C | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136074221 | TTTGGGAGGCCGAGG[A/C]GGGCAGATCACGAGG | 138151 |
rs112444508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136088102 | GTATTCGGGGACTGT[C/T]GGGCTTGTACGGTCG | 138151 |
rs112451021 | snp | C/T | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136074188 | AGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 138151 |
rs112453020 | snp | A/G | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136019619 | GCGCCCCCACACAGG[A/G]AAGGTGCACCAGGGT | 138151 |
rs112467449 | snp | A/T | 0.5 | 0 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007579 | CACGCGCACACGCAC[A/T]CTCTCACCCACGGAG | 138151 |
rs112468788 | snp | A/G | 0.496937 | 0.0390173 | intron-variant | NACC2 | GRCh38.p7 | 9:136069145 | ACTCCTGACCTTGTG[A/G]TCTGCCCGCCTCGGC | 138151 |
rs112519476 | in-del | -/A | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136072245 | CTCTGTCTCAAAAAG[-/A]AAAAAAAAAAAACCC | 138151 |
rs112554424 | in-del | -/GA | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136060916 | AGCCAGTCCCTGAGA[-/GA]CTGGGTACAGGGGTC | 138151 |
rs112597232 | in-del | -/C | 0.241627 | 0.24986 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096074 | GGCACGGAAATAAAA[-/C]ACGGCCACACACCCG | 138151 |
rs112609160 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NACC2 | GRCh38.p7 | 9:136091199 | TTCAGTGGCTTCACT[A/G]GCCCAACAGCCCCCA | 138151 |
rs112611816 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | NACC2 | GRCh38.p7 | 9:136057824 | TCACCACTGGGGCCG[A/G]GGGTTGTGGAAGCGG | 138151 |
rs112625863 | snp | A/G | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136074217 | GCACTTTGGGAGGCC[A/G]AGGAGGGCAGATCAC | 138151 |
rs112731206 | snp | C/G | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136095353 | GCGGGGGAGGTGCCC[C/G]CGGGCCGTTAAAGGG | 138151 |
rs112734024 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136037792 | AGGATTACAGGCATG[A/G]ACTACTGTGCTTGGC | 138151 |
rs112758206 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136044326 | TTCGAGGCCACCTGG[A/G]CAATATAGCGAGACC | 138151 |
rs112797608 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136076784 | GAGGCTGAGGTGGGT[A/G]GATCATGAGGTCAGG | 138151 |
rs112810032 | snp | C/G | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136070013 | TGTTCTTTTCACGTG[C/G]CTGTGGAACATATGC | 138151 |
rs112818454 | snp | C/T | 0.0158469 | 0.0875917 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008857 | CTGGCCCGCCCGGGG[C/T]GCAGGGAGAGCTCAG | 138151 |
rs112870461 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | NACC2 | GRCh38.p7 | 9:136020149 | TCACTGCAACGGCCC[C/T]TCTCACGTCCACTTT | 138151 |
rs112887766 | snp | C/T | 0.00526906 | 0.0510565 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012074 | GCCTGCCGGGAGGCC[C/T]GCCCCTCCCCAAGGC | 138151 |
rs112916066 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NACC2 | GRCh38.p7 | 9:136025629 | TAAAAAAAAAAAAAA[C/T]GCAGCCGGGCGCAGT | 138151 |
rs112977995 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136075487 | TCCGTGTGAACCTGC[C/T]GTCTCCTACATCGCG | 138151 |
rs112991719 | snp | G/T | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136023747 | CCTTTGCAAGAGCTT[G/T]TCCAGCCATAGGCAC | 138151 |
rs113024062 | snp | C/G | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136060486 | TTTCCAGAAGACAGG[C/G]CCAGGCCCAGGCCCC | 138151 |
rs113035890 | snp | A/T | 0.5 | 0 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007545 | GACGTGCACACACAG[A/T]CACGCACACACACAC | 138151 |
rs113069509 | snp | A/G | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136073195 | CTACACGGGAGGCTG[A/G]GGTGGGAGGATCACT | 138151 |
rs113093361 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | NACC2 | GRCh38.p7 | 9:136082798 | AGCGGATCCCACAGA[A/C]GCCCCGTTCTCTGGG | 138151 |
rs113106016 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136069410 | AAAAATTAGCCGGGC[A/G]TGGTGGCAGGCACCT | 138151 |
rs113126811 | snp | A/G | 0.00676609 | 0.0577691 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010371 | GGCCCAGCCCTGGCC[A/G]CTGCCTCCTGCCCGA | 138151 |
rs113130936 | snp | A/G | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136017042 | CTCAGTGCATCCAAG[A/G]ACACAGCCCTGGGAC | 138151 |
rs113153235 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NACC2 | GRCh38.p7 | 9:136082339 | TCCGGGCTCTGCCCC[A/G]CCTGTGCCACGTGCT | 138151 |
rs113156938 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NACC2 | GRCh38.p7 | 9:136090683 | CTGACTATGGAGGGC[C/T]GGGGGGACTTTTATT | 138151 |
rs113185846 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | NACC2 | GRCh38.p7 | 9:136071168 | AACCTGGGAGGCAGA[C/T]GTTGCGGTGAGCCAA | 138151 |
rs113240000 | snp | C/T | 0.5 | 0 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014924 | TGAACCCTCTGGGAA[C/T]AATGGGGAGGGAATG | 138151 |
rs113247036 | snp | A/G | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136066530 | ATGTAAAGAGATGTA[A/G]CGATCGGGAATGCAA | 138151 |
rs113271630 | snp | C/G | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136077214 | CGGGCGCCTGTAGTC[C/G]CAGCCACTTGGGAGG | 138151 |
rs113355235 | snp | G/T | 0.0341408 | 0.126114 | intron-variant | NACC2 | GRCh38.p7 | 9:136089537 | CCCCCAGCGCTGGGG[G/T]CCTCTCCCCAAGAAG | 138151 |
rs113360983 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136044929 | GGGGGATGGACGGGG[C/T]CAGTGCTGACCTTGC | 138151 |
rs113383777 | snp | A/G | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136066893 | GTCACAAGAGGGCAC[A/G]TATTATGAGATTCCA | 138151 |
rs113398630 | snp | A/G | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136074211 | ATCCCAGCACTTTGG[A/G]AGGCCGAGGAGGGCA | 138151 |
rs113410268 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009818 | CGCTGGTCGGCCACC[A/G]CTCACTGGCCTGTGT | 138151 |
rs113433532 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | NACC2 | GRCh38.p7 | 9:136062714 | GAGCCCAGCAGTTCA[A/C]GACTAGCCTGGGCAA | 138151 |
rs113507139 | in-del | -/ATTC/ATTCATTCATTA/ATTT | 0.0659589 | 0.169201 | intron-variant | NACC2 | GRCh38.p7 | 9:136031342 | TTCATTCATTCATTC[-/ATTC/ATTCATTCATTA/ATTT]ATTCATTCATTCTGA | 138151 |
rs113512697 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136023102 | GAAGGAGGGAAGAGG[A/G]AGGGAGGAGGGAGGG | 138151 |
rs113522629 | snp | A/C | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136069857 | TAAAGACAAACCCAC[A/C]ATTCTAGTAGAGACT | 138151 |
rs113598056 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NACC2 | GRCh38.p7 | 9:136075999 | AACTCCGAGACACCC[A/G]CTTCTCAAAGCCCTG | 138151 |
rs113609675 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136023140 | GGAGGGAGGAAGGAC[C/T]TGTACGCATATCCTG | 138151 |
rs113673685 | snp | C/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007460 | ACACACACGCGCACA[C/G]AGACGCACACACACA | 138151 |
rs113697589 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136087874 | AGGGAGGGCAAGCCC[C/T]CCCCGTCCCTTGTCT | 138151 |
rs113709326 | snp | C/T | 0 | 0 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009409 | TGGATGCCTCTGCAC[C/T]ACTGAGCCACCTGCA | 138151 |
rs113735259 | snp | C/G | 0.0482946 | 0.147699 | intron-variant | NACC2 | GRCh38.p7 | 9:136069099 | TTTTAGTAGAGACGG[C/G]GTTTCACCAAGTTGG | 138151 |
rs113750818 | in-del | -/T | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136079058 | AATCATAGCTTCTTC[-/T]TTTTTTTTTTTTTTA | 138151 |
rs113770855 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136034913 | AGCCTGGCCAACATG[C/G]TGAAACCCCATCTCT | 138151 |
rs113816024 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | NACC2 | GRCh38.p7 | 9:136071273 | AAAAAGGCTGGGCGC[A/G]GTGGCTCACGCCTAT | 138151 |
rs113825490 | snp | A/G | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136063058 | CACTGTTTTCTTCTA[A/G]TTTTTGTTCTCGTTG | 138151 |
rs113867040 | snp | C/T | 0.5 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136074232 | GAGGAGGGCAGATCA[C/T]GAGGTCAGGAGATCC | 138151 |
rs113891218 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NACC2 | GRCh38.p7 | 9:136056875 | AGCTTTCTTCCCAGA[C/T]GGAGAAGGGCAGTAC | 138151 |
rs113914268 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136016609 | GACTGGCTTCAGCCT[A/G]CCCCATCCCTACTTG | 138151 |
rs113919820 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | NACC2 | GRCh38.p7 | 9:136084393 | CCATCACACAGACAC[C/T]TCCTACGCAATGTCC | 138151 |
rs113972374 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NACC2 | GRCh38.p7 | 9:136066044 | ACTAAAAATACAAAA[C/T]TAGCCGGGTGTGGTG | 138151 |
rs114018130 | snp | C/G | 0.0517044 | 0.152246 | intron-variant | NACC2 | GRCh38.p7 | 9:136080736 | GTCTCCTCCTCTCCA[C/G]ACACGTGGAGACGGG | 138151 |
rs114186415 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | NACC2 | GRCh38.p7 | 9:136083136 | CGATGCCAGAAACGG[A/G]GCCACCCTGCTGGAG | 138151 |
rs114187237 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | NACC2 | GRCh38.p7 | 9:136071914 | AGACGCAAATGTGCT[A/G]AACTCCACCCAAGCC | 138151 |
rs114192884 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | NACC2 | GRCh38.p7 | 9:136017197 | GCTGGGGCAGATGAC[A/G]GCCAGGCGCCCTGCA | 138151 |
rs114272216 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | NACC2 | GRCh38.p7 | 9:136087936 | CCCAGTTTCCCACCC[C/T]GGGGACTCTGCTGGG | 138151 |
rs114300341 | snp | C/T | 0.0337553 | 0.125452 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015971 | CGCGGGGCGGGGGGA[C/T]TGGCAACTATACGTG | 138151 |
rs114303995 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012396 | CCCCTCCCCGTCCCA[A/G]TCCCAGCCTGGAGGA | 138151 |
rs114329830 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NACC2 | GRCh38.p7 | 9:136059612 | CGTCCAGGTCAGCAG[A/G]CCCAGCAAGGAACCT | 138151 |
rs114372821 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | NACC2 | GRCh38.p7 | 9:136088607 | GTTAACCATCAGCAG[A/G]GGCTTCACTGCCATC | 138151 |
rs114393934 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | NACC2 | GRCh38.p7 | 9:136029308 | CTCAGCTGAGAGCTG[A/G]GCAGATGTTGAGGAG | 138151 |
rs114459358 | snp | A/T | 0.0341408 | 0.126114 | intron-variant | NACC2 | GRCh38.p7 | 9:136092026 | CAGGCTGAAAGGGAA[A/T]CGAGATCCACCTGGG | 138151 |
rs114476111 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | NACC2 | GRCh38.p7 | 9:136086293 | AGGGCACATGCCCCC[C/T]GAGGCCTCCCACTCA | 138151 |
rs114494920 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | NACC2 | GRCh38.p7 | 9:136023416 | GCTTCTCGACCAGCT[C/T]AACAGTCCCATCAAA | 138151 |
rs114501032 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | NACC2 | GRCh38.p7 | 9:136049081 | CTCCAATTAGGGCAA[C/T]CTGGGTTTGTGGGGC | 138151 |
rs114515730 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | NACC2 | GRCh38.p7 | 9:136080603 | TAAAAAAACTCCAAC[A/G]CTACTGCCAGCACAC | 138151 |
rs114516920 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NACC2 | GRCh38.p7 | 9:136063927 | ATCACTTAAACAGCT[A/G]TGCCCTCATCGGCTA | 138151 |
rs114577364 | snp | A/G | 0.030278 | 0.119257 | intron-variant | NACC2 | GRCh38.p7 | 9:136091815 | AGAGCCAGGGCTGGT[A/G]AGAGCAAGGATTTGC | 138151 |
rs114697501 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | NACC2 | GRCh38.p7 | 9:136056655 | GGGTCACAGAGGTAC[A/G]GGGGGTCTCTGGGAT | 138151 |
rs114766248 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | NACC2 | GRCh38.p7 | 9:136086193 | GAATGTGGCCAGGAC[C/T]CTCCATGGGCCTTCA | 138151 |
rs114769230 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | NACC2 | GRCh38.p7 | 9:136087742 | GCTCGAATCCCAAGA[C/G]AACACTTGCTCTCCA | 138151 |
rs114799500 | snp | G/T | 0.030278 | 0.119257 | intron-variant | NACC2 | GRCh38.p7 | 9:136084650 | CGCCACGTCCATAGC[G/T]GCAGCACCAGACAGC | 138151 |
rs114824679 | snp | A/G | 0.304688 | 0.243945 | intron-variant | NACC2 | GRCh38.p7 | 9:136094736 | AGATGCGCCGGGAGG[A/G]GTGGGTACCTCCGCC | 138151 |
rs114908852 | snp | A/C | 0.0479149 | 0.147179 | intron-variant | NACC2 | GRCh38.p7 | 9:136021797 | CAAATGATTGGCACA[A/C]AACCTGGATGGATCT | 138151 |
rs114916546 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | NACC2 | GRCh38.p7 | 9:136030252 | TACAAAAACAGGACA[C/T]GGGACAGATCTGCCA | 138151 |
rs114977604 | snp | C/G | 0.0414363 | 0.137845 | intron-variant | NACC2 | GRCh38.p7 | 9:136029837 | GCTCGCTCACACACC[C/G]CTTGCTGCTCTGTGC | 138151 |
rs114989873 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | NACC2 | GRCh38.p7 | 9:136082709 | AACCCCAACAGGGGC[A/G]CAGCCCTCAATCCAG | 138151 |
rs114997172 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136060077 | CGCATCTGCCCTGGC[A/G]GCATGCCCAGACCTA | 138151 |
rs115035716 | snp | A/G | 0.021333 | 0.101051 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007943 | CCCTCCCTACCTTCC[A/G]CCTTCCTCCTGGCTC | 138151 |
rs115081918 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | NACC2 | GRCh38.p7 | 9:136088384 | GGGCAAAAATTTGAG[C/T]CCACACAGCAATGCT | 138151 |
rs115089740 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | NACC2 | GRCh38.p7 | 9:136085596 | GGTGTAAGGCCAGGA[A/G]GGGCCTGGGAGGCGG | 138151 |
rs115183972 | snp | C/T | 0.0596104 | 0.162024 | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006241 | CTGGCAGGTTGCCTG[C/T]GGGTCCGGACAGGGC | 138151 |
rs115186399 | snp | A/T | 0.030278 | 0.119257 | intron-variant | NACC2 | GRCh38.p7 | 9:136094497 | CGGCGGGCCCCGGGC[A/T]CCGCTGAGTTTCTTA | 138151 |
rs115235702 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | NACC2 | GRCh38.p7 | 9:136086221 | TCAGAGCAGCAAAGC[A/G]CAGTGCCTGCCTTCC | 138151 |
rs115308744 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | NACC2 | GRCh38.p7 | 9:136075459 | TTTCCCTTTCGTAGA[C/T]GTCGGCAGCGGCTCC | 138151 |
rs115339046 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136021665 | AGGAACGCTTATCCC[A/G]TCTCTACTCTTGAAT | 138151 |
rs115372382 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NACC2 | GRCh38.p7 | 9:136055752 | CGTGGTAGAGGAAGG[A/G]GAGAGGCGGGGCACG | 138151 |
rs115374734 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | NACC2 | GRCh38.p7 | 9:136017189 | AAACCACTGCTGGGG[C/T]AGATGACGGCCAGGC | 138151 |
rs115422425 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | NACC2 | GRCh38.p7 | 9:136081712 | AGGAACACACACAGC[C/T]CCTCCTGGCTCGGGC | 138151 |
rs115579596 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | NACC2 | GRCh38.p7 | 9:136084531 | ATCAAATCTGTCAAA[C/T]TGGCCCAGACCCCGG | 138151 |
rs115625941 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | NACC2 | GRCh38.p7 | 9:136084750 | ACACATACATCACGC[A/C]GCCTGGAGAAGGGAC | 138151 |
rs115757377 | snp | C/T | 0.0711525 | 0.174681 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015738 | TGGCGTGGGTCAGAC[C/T]GGCTTTAGCCTGCCC | 138151 |
rs115869428 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | NACC2 | GRCh38.p7 | 9:136023370 | CAGCTCTCGGAGAAC[A/G]TGGGATCCCCGAGTG | 138151 |
rs115921483 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | NACC2 | GRCh38.p7 | 9:136020581 | GCCTACTCCCTAAAA[C/G]TGTATACCATTTGTT | 138151 |
rs116020496 | snp | A/G | 0.030278 | 0.119257 | intron-variant | NACC2 | GRCh38.p7 | 9:136082402 | TTCACCTGCCTCCCC[A/G]CCATGCCTGTGAGAG | 138151 |
rs116032001 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NACC2 | GRCh38.p7 | 9:136031899 | TCTAACTGTGAGGTT[C/T]TGGCATCTGCACCAA | 138151 |
rs116080954 | snp | C/T | 0.0142736 | 0.0832652 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096614 | TAGACCTAAATGCAG[C/T]CCCAGGTCCCACACC | 138151 |
rs116085000 | snp | C/G | 0.0221141 | 0.102801 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015187 | CAAACAGAGGCCACA[C/G]CTGCTGGAGGCTGGG | 138151 |
rs116096125 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NACC2 | GRCh38.p7 | 9:136084729 | AATGGCGGCGGGCGC[A/G]CACACACACATACAT | 138151 |
rs116130720 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | NACC2 | GRCh38.p7 | 9:136085180 | GCGAGACTGAGTTTC[A/G]CTCTTGTCGCCCAGG | 138151 |
rs116170565 | snp | C/G/T | 0.0490732 | 0.148853 | intron-variant | NACC2 | GRCh38.p7 | 9:136019271 | ACGGCTCATCCCTCG[C/G/T]GGCCCCCGGAAGGGC | 138151 |
rs116247903 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NACC2 | GRCh38.p7 | 9:136094337 | TTTAAGCGGCTCCAC[A/G]ACGAGAGTCCAAGAC | 138151 |
rs116275071 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NACC2 | GRCh38.p7 | 9:136084430 | CGCTGGTGGGGCAAC[A/G]TCCAAGAAGGCGGTA | 138151 |
rs116282806 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | NACC2 | GRCh38.p7 | 9:136056132 | CGGAGGTTAACCCTG[G/T]GGGGTAGAGGCTGCC | 138151 |
rs116287392 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007335 | TGCTCCGGTGGTGAC[A/G]TGCACGCGCGTGCAC | 138151 |
rs116339818 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | NACC2 | GRCh38.p7 | 9:136073734 | TGTGTGCTACAATTT[C/T]GGCACAATTTGCTCA | 138151 |
rs116419192 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | NACC2 | GRCh38.p7 | 9:136023315 | CCCGACGCGAGGGGC[C/T]GGCATGACCCTGCAG | 138151 |
rs116454509 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | NACC2 | GRCh38.p7 | 9:136085052 | CTGAAAAAGCTAAAA[C/T]GGTAAATTTTATGTA | 138151 |
rs116563169 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | NACC2 | GRCh38.p7 | 9:136067392 | AAGATGTTCTAAAAT[C/T]CACGATGGTAATGGT | 138151 |
rs116563828 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | NACC2 | GRCh38.p7 | 9:136017620 | ATCAGCTCCCCTGAG[C/T]GGGCCCCCGGTGCTC | 138151 |
rs116567265 | snp | A/G | 0.0829062 | 0.185956 | intron-variant | NACC2 | GRCh38.p7 | 9:136073204 | AGGCTGGGGTGGGAG[A/G]ATCACTTGAGCCCAA | 138151 |
rs116622687 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NACC2 | GRCh38.p7 | 9:136087829 | CAACGAGGCCCCAAG[C/T]GCCCTGTCCTCCCCG | 138151 |
rs116647079 | snp | A/G | 0.0763149 | 0.179815 | intron-variant | NACC2 | GRCh38.p7 | 9:136075270 | ATTCTGGTCCAGTCC[A/G]GCACTGACCGGGATG | 138151 |
rs116674318 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | NACC2 | GRCh38.p7 | 9:136083301 | AGCCTAGGCACGCGG[A/T]GGTCATCTCCTTGCT | 138151 |
rs116676200 | snp | C/T | 0.16911 | 0.236552 | intron-variant | NACC2 | GRCh38.p7 | 9:136048904 | CTGGCATTATGCACC[C/T]GCACCCAGGCCCAGG | 138151 |
rs116736338 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136023108 | GGGAAGAGGGAGGGA[C/G]GAGGGAGGGGGAGGA | 138151 |
rs116819366 | snp | C/G | 0.0279526 | 0.114869 | intron-variant | NACC2 | GRCh38.p7 | 9:136030629 | AAAAAATAAAAAGAG[C/G]GTACTGGAACAATTT | 138151 |
rs116866113 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | NACC2 | GRCh38.p7 | 9:136062871 | GCAGTGTGCCGTGAT[C/T]GTGCCACTGTACTCC | 138151 |
rs116973826 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | NACC2 | GRCh38.p7 | 9:136077991 | GTTAGCCAGGCTGGT[C/G]TCAAACTCCTGACCT | 138151 |
rs117022226 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | NACC2 | GRCh38.p7 | 9:136067814 | CCTCCAGTCTGGCAA[C/T]AGGGCGAGACGCCAT | 138151 |
rs117076996 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136085000 | AGTTCTAGAGATGGT[A/G]CTGAGGGCAGCGCAA | 138151 |
rs117083962 | snp | A/G | 0.00953873 | 0.0683987 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007632 | GTATGCAGCAGCAAC[A/G]TTCTGAAACAGTAGT | 138151 |
rs117100567 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009863 | GTGCTGATGGGCGCA[A/G]GGCTGCACTTGTTTT | 138151 |
rs117116359 | snp | C/T | 0.00874735 | 0.0655527 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011057 | GCCTGAGCCCTGCCC[C/T]GTCGCCCCAGAGAGG | 138151 |
rs117162508 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NACC2 | GRCh38.p7 | 9:136060383 | ATAAAAGGTAATTAC[C/T]GATATGAAAAATAAA | 138151 |
rs117259715 | snp | A/G | 0.0103295 | 0.0711199 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096247 | TCAGTGGTCCCGAGC[A/G]AGGGCGCTGGGAGAA | 138151 |
rs117363221 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NACC2 | GRCh38.p7 | 9:136064711 | TTTGCCAACATTGTC[A/G]AGCTGATGCTAAAAA | 138151 |
rs117411421 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | NACC2 | GRCh38.p7 | 9:136081983 | GTGGAGCTGACGCGA[A/G]AGCCAGGCTGCAGCA | 138151 |
rs117422905 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | NACC2 | GRCh38.p7 | 9:136092689 | AGGTGGACTGGGCCG[C/G]AGGAGCAGCAGAGTC | 138151 |
rs117522807 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | NACC2 | GRCh38.p7 | 9:136066218 | AAAGAAAGAAAGAAA[A/G]AGAAACCAAAGAATA | 138151 |
rs117654243 | snp | A/G | 0.00597247 | 0.0543191 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009330 | ACCTGTGCCCAAGAC[A/G]GGGGAGGAAGAGGCA | 138151 |
rs117660618 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136078346 | TGAGGGGGACAGGCA[C/T]ATCTGGGGGCAGGTT | 138151 |
rs117675937 | snp | A/G | 0.079617 | 0.182947 | intron-variant | NACC2 | GRCh38.p7 | 9:136073289 | AAATAAACTAGCTGG[A/G]CATGGTGGAGCGCAC | 138151 |
rs117711787 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NACC2 | GRCh38.p7 | 9:136084146 | TGGATCCAGCCAGGA[A/G]GGGACCCGTCTTTCC | 138151 |
rs117815158 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | NACC2 | GRCh38.p7 | 9:136074935 | GGTTCTCGCACGGCC[A/T]CCTTCTGGGAGCCCG | 138151 |
rs117956982 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | NACC2 | GRCh38.p7 | 9:136070233 | CAAATACGGGCCGGG[C/T]GTGGTGGCTCACGCC | 138151 |
rs117986720 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136066580 | GAAAACAGTCTGGAA[C/T]TTCCTCAAAAGGTCA | 138151 |
rs118065742 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | NACC2 | GRCh38.p7 | 9:136063158 | TCTCTCCTGTCAAAC[A/G]TGTGGTTTGAGCCGC | 138151 |
rs118080101 | snp | A/G | 0.0279526 | 0.114869 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008033 | TCCTATGTTCTAGGA[A/G]CCCCGACCCGCAGTC | 138151 |
rs118111405 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NACC2 | GRCh38.p7 | 9:136087949 | CCCGGGGACTCTGCT[A/G]GGAAGTTCCGGGAGG | 138151 |
rs118189089 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | NACC2 | GRCh38.p7 | 9:136056252 | CAGAGCTGGGCTGCC[C/T]GGAGGCCTGGCTGCT | 138151 |
rs118191653 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136093235 | CCAAGAGGAGTGCAG[A/G]CCTGGAAGAACCGCT | 138151 |
rs137862968 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NACC2 | GRCh38.p7 | 9:136088703 | CTGAGACACAGGGAG[A/G]CAAAGGACTTGGTCT | 138151 |
rs137902208 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NACC2 | GRCh38.p7 | 9:136017027 | CAAGGACACGGGGGA[C/T]TCAGTGCATCCAAGA | 138151 |
rs137948502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136020493 | TGTGCGGATGTGGGC[A/G]GCAGTGGCGAGTGGT | 138151 |
rs137977258 | snp | A/G | 0.0154538 | 0.0865337 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008071 | CCGGCACCCCCAGGC[A/G]GGTCCTGCTGACCTC | 138151 |
rs138080451 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136083521 | AAGATCAAGTTCACA[C/T]GAGAGCTTCCCAGAT | 138151 |
rs138082541 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136056524 | GCCAGAGAGGATGCC[C/T]GGCCCCGCCCAACAG | 138151 |
rs138183467 | snp | C/G/T | 0.0150606 | 0.0854603 | intron-variant | NACC2 | GRCh38.p7 | 9:136075324 | TGGCTGGGATACTTG[C/G/T]GGGGAAAGCCCTCCC | 138151 |
rs138208625 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NACC2 | GRCh38.p7 | 9:136059937 | CAGCAGAGAGGGGCC[A/G]CACCCTGTCCCCTCC | 138151 |
rs138209225 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NACC2 | GRCh38.p7 | 9:136032483 | CCTACTTAAAGAGGA[A/G]CAGTGGAAGCTTTTC | 138151 |
rs138226073 | in-del | -/C/GC | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010896 | ACCCCGAGGGGTGGG[-/C/GC]CCACAGCCATCACTG | 138151 |
rs138257259 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136093130 | CTCAACATCCCGAAA[A/T]GGACAACACCTTGGT | 138151 |
rs138390772 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | NACC2 | GRCh38.p7 | 9:136070203 | CATATGTCAAAGAAG[A/T]AGTCTCAAGAAAATC | 138151 |
rs138472176 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136084766 | GCCTGGAGAAGGGAC[A/G]GGCTCCGCCACTCCC | 138151 |
rs138498900 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | NACC2 | GRCh38.p7 | 9:136072169 | CTTGAAACCGGGAGG[C/T]GGAGGTTGCAGTTAG | 138151 |
rs138500528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136021763 | ACATGACGTGTTACC[A/G]CTTGGCTGTGAAAAG | 138151 |
rs138543194 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NACC2 | GRCh38.p7 | 9:136065577 | GTGAGCCAAGATTGC[A/G]CCACTGCACTCCAGC | 138151 |
rs138560606 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | NACC2 | GRCh38.p7 | 9:136024727 | GAGATTCCCACTGTG[C/G]ATATGAGGGAGCAGC | 138151 |
rs138586269 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016172 | TTTTTTGACTGATTG[A/G]TGATGAGTACATTGT | 138151 |
rs138608019 | in-del | -/CA | 0.0130921 | 0.0798413 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007348 | ACGTGCACGCGCGTG[-/CA]CACACACAGACACAC | 138151 |
rs138748334 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NACC2 | GRCh38.p7 | 9:136072785 | AACTCAGGAGGCGGA[C/G]GCTGTGGTGAGCCTA | 138151 |
rs138803627 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NACC2 | GRCh38.p7 | 9:136074832 | GTATCACTCAGCCTC[A/G]GCGTCTACACCTCAC | 138151 |
rs138863603 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136062638 | AAATTATACAGGCTG[G/T]GCACAGTGGCTCATG | 138151 |
rs138896616 | in-del | -/GA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136066206 | TCAAAAAAAAAAAAA[-/GA]AAGAAAGAAAAAGAA | 138151 |
rs138911367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136029742 | CCTGCAGGGAGCCGG[C/T]GCCTGTGCCAGTGCC | 138151 |
rs138946605 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | NACC2 | GRCh38.p7 | 9:136017329 | GAGGTCCCTGGGCAG[C/G]ACTCTCTGCTGTCAG | 138151 |
rs139012191 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NACC2 | GRCh38.p7 | 9:136063234 | CCCTGGGCTGGTCTC[A/G]GCCATGCTGTGCAGA | 138151 |
rs139013265 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NACC2 | GRCh38.p7 | 9:136092685 | GTGAAGGTGGACTGG[A/G]CCGGAGGAGCAGCAG | 138151 |
rs139020800 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136089389 | AAACCTAGCACCCGC[A/G]AAGGCCTGACTTCCA | 138151 |
rs139120385 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136094450 | GAAACTCCGTCGGAA[A/G]GCCTCGGTCCGCCCT | 138151 |
rs139182963 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NACC2 | GRCh38.p7 | 9:136071213 | ACTCCATCCAGCCTG[A/G]GAGACAGAGCAAGAC | 138151 |
rs139236528 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NACC2 | GRCh38.p7 | 9:136026156 | ACCAGCTTGGCTAAC[A/G]TGGCAAAACTCCGTC | 138151 |
rs139277052 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074028 | ATTAAGATCTTGGCC[A/G]GGCACAGTGGCTCAT | 138151 |
rs139294414 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136061743 | GAAGCCAGGTGGGTG[A/G]GCGGGGACAAGCACA | 138151 |
rs139351456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136070063 | GGCCAGAAAGAAAAC[C/T]TCAAGAACTTTACAA | 138151 |
rs139399777 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | NACC2 | GRCh38.p7 | 9:136057262 | CCAACACGCTCATCT[C/G]TAACCTTCACTTGCA | 138151 |
rs139408567 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NACC2 | GRCh38.p7 | 9:136030253 | ACAAAAACAGGACAC[A/G]GGACAGATCTGCCAT | 138151 |
rs139420339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136026720 | TCTAACTCAGGATGA[A/G]TGCTGAAATCCCTAA | 138151 |
rs139485529 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136026173 | GGCAAAACTCCGTCT[C/T]TACTAAAAATACAAA | 138151 |
rs139503832 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136076245 | GTTTCCCGGCCCTGC[A/G]GAACTCGAAGAAGTG | 138151 |
rs139534285 | snp | A/G/T | 0.000128403 | 0.00801155 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011861 | GGGCACGCTGGCGGC[A/G/T]GCGGAGCCCATGACC | 138151 |
rs139550655 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NACC2 | GRCh38.p7 | 9:136030920 | TGCCCACCTCAGCCT[C/T]GCAGTGCTGGGATTA | 138151 |
rs139555936 | in-del | -/TGTG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024504 | TGTGTGAGGACAGAA[-/TGTG]TGTGTGTGTGTGTGT | 138151 |
rs139577741 | in-del | -/TC | 0.0322114 | 0.122752 | intron-variant | NACC2 | GRCh38.p7 | 9:136060423 | TACAAACACCCAACT[-/TC]TACAGCTCGGGAATG | 138151 |
rs139665301 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NACC2 | GRCh38.p7 | 9:136091182 | GTGAGCCTTACATGG[A/G]ATTCAGTGGCTTCAC | 138151 |
rs139677488 | in-del | -/CA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136077600 | AAGAAAAGGGAAACG[-/CA]CAGAGGAGGGAGGGG | 138151 |
rs139755169 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010385 | CGCTGCCTCCTGCCC[A/G]AGCGGAGTCCCCCGC | 138151 |
rs139764759 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009811 | TGGGGTGCGCTGGTC[A/G]GCCACCGCTCACTGG | 138151 |
rs139782132 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136081484 | CCAGGAAGGCGGTGC[C/T]GGGCGTCCGCTTCCA | 138151 |
rs139822183 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136063955 | CTAGAAGATACTGTG[A/C]AACTTTACAAATCTA | 138151 |
rs139916490 | snp | A/G | 0.000307953 | 0.0124049 | synonymous-codon, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013209 | CTTACATTTCACAGC[A/G]TTCAGGACCCGGCTG | 138151 |
rs139930326 | in-del | -/ACAGACGCACAT | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007554 | CACAGACACGCACAC[-/ACAGACGCACAT]ACACACAGACACGCG | 138151 |
rs139971892 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136078110 | GGTTTGCCGTACTAT[C/T]TTTAAACAATCCATG | 138151 |
rs139974646 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NACC2 | GRCh38.p7 | 9:136017962 | CTGGACCTTGCTTGC[C/T]GAGGGCACGGCATGG | 138151 |
rs139987488 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136068167 | GACTGTATAAACACC[A/G]AACATTTAGGCTACA | 138151 |
rs139987717 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015144 | TCATAAACTGAAGCA[C/T]GTCTCCAATCCCATC | 138151 |
rs140004205 | in-del | -/CACAGACGCA | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007455 | GCGCACACACACGCG[-/CACAGACGCA]CACACAGACGCACAC | 138151 |
rs140067700 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | NACC2 | GRCh38.p7 | 9:136082086 | AGCCATTCTCCAAAG[A/C]CTCTCCACCTGAACA | 138151 |
rs140114982 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136057587 | TAACGTAAGCTTGAA[A/G]AGCGTCTCCCTCGGG | 138151 |
rs140186110 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | NACC2 | GRCh38.p7 | 9:136061202 | GTGCCGGCTACCGGG[C/G]TCTCCCACTGCCTGG | 138151 |
rs140213572 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136067178 | AGAATCGCTTGAACC[C/T]GGGAGGCGGACGTTG | 138151 |
rs140264366 | in-del | -/GACAGGACAGGACAGGACAG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136062115 | TGGGCAACAGAGCGA[-/GACAGGACAGGACAGGACAG]GACAGGACAGGACAG | 138151 |
rs140270572 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | NACC2 | GRCh38.p7 | 9:136037965 | TTAACCAGTGAATGC[A/G]TACACAAATTGTGGT | 138151 |
rs140280601 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136019951 | GCGGCCCCCAGAGTC[G/T]TCAGGTCCACAGAGG | 138151 |
rs140311661 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NACC2 | GRCh38.p7 | 9:136062671 | TGTAATCCCAACATT[C/T]TGGGAGGTCAGCGGG | 138151 |
rs140314660 | snp | A/C/T | 6.80172e-05 | 0.00583135 | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016474 | GGGCATCTGGGGGGC[A/C/T]GGGCTGCTCTGTGCC | 138151 |
rs140314787 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136069273 | TTCTATTGACTGGGC[A/G]CGGTGGCTCACACCT | 138151 |
rs140414618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136066598 | CCTCAAAAGGTCAAA[C/T]AGAATTCCTACATGA | 138151 |
rs140512407 | in-del | -/TACA | 0.030278 | 0.119257 | intron-variant | NACC2 | GRCh38.p7 | 9:136073129 | GACTAATATCTAGGC[-/TACA]TAAAGAATTAATTGG | 138151 |
rs140527098 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136032262 | CCAGGAATACGAAGT[C/T]ATTTCAATATTTGGA | 138151 |
rs140631283 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | NACC2 | GRCh38.p7 | 9:136057911 | CTGGGCCCCGCTGCT[G/T]GTCACCCAGCCCATT | 138151 |
rs140651085 | in-del | -/TCAT/TCATTCATTCAT/TCATTCATTCATTCAT | 0.179744 | 0.239925 | intron-variant | NACC2 | GRCh38.p7 | 9:136031324 | CTTTACTCCACAGCC[lengthTooLong]TCATTCATTCATTCA | 138151 |
rs140664773 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136090184 | AGCTGGGTGGTAGAA[G/T]GGAGATGGGCACAGC | 138151 |
rs140676815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136018463 | GCAGCAGGTGTTCCA[C/T]TCCTGAGAACCATGC | 138151 |
rs140757727 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136092045 | GATCCACCTGGGGAT[C/T]AGGGGGCGCCTCAGG | 138151 |
rs140800141 | snp | A/G | 0.040671 | 0.13668 | intron-variant | NACC2 | GRCh38.p7 | 9:136065395 | GAGGCCGAGGCGGGC[A/G]GATCACTTGAGGTCA | 138151 |
rs140817607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136022314 | GGAGATGACCACACT[C/T]TCCACATGGGGCTGT | 138151 |
rs140861612 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136093251 | CCTGGAAGAACCGCT[C/G]AGCACCAAGATCGTC | 138151 |
rs140886814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067025 | GGAGGTCAAGGCAGG[C/T]GGATCACCTGAGGTC | 138151 |
rs140905837 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136019391 | TGCCGGTCACACTGA[C/G]GTCCCTCCTGAGCCT | 138151 |
rs140951439 | snp | G/T | 0.021333 | 0.101051 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096374 | CAAGGTCATTCCCTG[G/T]ACAAATCATCAGAAG | 138151 |
rs141050138 | in-del | -/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008108 | ACAGCTTTGTCCACA[-/T]TCAGGGGCAAAGTAC | 138151 |
rs141146386 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136057086 | AGGACGCTCCATCCT[C/T]GGCAGCAGCAGGCTC | 138151 |
rs141201668 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | NACC2 | GRCh38.p7 | 9:136047132 | CAGAGAGACAGCTAC[C/T]TGCCTCCACTCCTGC | 138151 |
rs141201857 | in-del | -/TAAA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136072858 | CCGTCTCAAATAAAT[-/TAAA]AAATAAATAAATAAC | 138151 |
rs141321337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136079120 | CCTGAAATCTACTCA[C/T]GTATGTCTGTGCGTC | 138151 |
rs141410972 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NACC2 | GRCh38.p7 | 9:136072511 | GATCACACCACTGCA[A/G]TCCAGCCTGCACAAC | 138151 |
rs141413948 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015637 | GTGGCCAAGGAAAGC[A/G]CCTGAGGGCCCAAGC | 138151 |
rs141470306 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | NACC2 | GRCh38.p7 | 9:136083142 | CAGAAACGGGGCCAC[A/C]CTGCTGGAGCGGAGG | 138151 |
rs141485195 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136026088 | CTCACACCTGTAACC[C/T]CAGCACTTTGGGAGG | 138151 |
rs141490860 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012788 | TTCCACATCTGGGGC[G/T]CGGGCCGGGGGCGGC | 138151 |
rs141516373 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010997 | GCCCGGTGGGCCTGG[C/T]CCCGAGTCTCCGAAA | 138151 |
rs141544649 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009291 | GTCCAGGTTCCCAGC[A/G]GGCCCCATGGGGGCT | 138151 |
rs141544810 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136065606 | GCCTGGGTGACAAAG[C/T]GAGACGCGGTTTCAG | 138151 |
rs141590268 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136092886 | TCGGAACCCACTGCG[C/T]GACCCTGCAAAGGGG | 138151 |
rs141601183 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NACC2 | GRCh38.p7 | 9:136021531 | AAAGTGGCATGGCCA[C/T]TCTGGAAAACTGCTT | 138151 |
rs141640551 | snp | C/G | 0.030278 | 0.119257 | intron-variant | NACC2 | GRCh38.p7 | 9:136060663 | ATGCTTAGCCCCGTC[C/G]GGTCTCAAAGGTGCC | 138151 |
rs141661559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136077832 | TTGAAAAGTGAATAA[A/G]GAATCAGTGATGAAT | 138151 |
rs141673364 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012203 | ACGTTTCTCACTGCT[C/T]GGCCTGGGAGGCCTC | 138151 |
rs141729475 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136076037 | GTTACGTGTGGTCAC[A/G]AAGAGATCCTGCAAA | 138151 |
rs141766835 | in-del | -/GAGGGAGGGAAGAGA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136023078 | GGAAGAGGGAGGGAG[-/GAGGGAGGGAAGAGA]GAGGGAGGGAAGGAG | 138151 |
rs141875132 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NACC2 | GRCh38.p7 | 9:136089880 | GACATGACACAGGCA[A/G]GATTAATGCCTAAAG | 138151 |
rs141905309 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | NACC2 | GRCh38.p7 | 9:136070204 | ATATGTCAAAGAAGA[A/C]GTCTCAAGAAAATCA | 138151 |
rs141906123 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | NACC2 | GRCh38.p7 | 9:136072110 | GGGCATGGTGATGTG[C/T]GCCTATAATCCCAGC | 138151 |
rs142200223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136094062 | AACACCAAGGTGCAC[A/G]CGCTCCCGGAGGCAG | 138151 |
rs142221492 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078152 | AGACACAGTGGTAGA[C/G]AGTGGGATGGACCAG | 138151 |
rs142239181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136023765 | CAGCCATAGGCACAG[A/G]TTGAATCAATCCCAC | 138151 |
rs142259185 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | NACC2 | GRCh38.p7 | 9:136064257 | CTGCACTACTGCACT[C/G]CAGCCTGGGTGACAG | 138151 |
rs142283292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136018584 | GTCAGTCCCAGGAAG[A/G]GGAGCTTCCCAAGGC | 138151 |
rs142351213 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | NACC2 | GRCh38.p7 | 9:136087917 | CGGCCGTGGCCCAGG[A/C]AGGCCCAGTTTCCCA | 138151 |
rs142370299 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NACC2 | GRCh38.p7 | 9:136017239 | TGCAGCTGTGCAGCG[C/T]GACCCCGATGGCACC | 138151 |
rs142405584 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | NACC2 | GRCh38.p7 | 9:136086825 | GCGGCTGCTGTCTGT[C/G]CCTGGCTCCTCCCAC | 138151 |
rs142415911 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014880 | CCACCAGGGTCTGGG[C/T]GAGCGAGGGCATGGA | 138151 |
rs142611363 | in-del | -/CT | 0.0562307 | 0.157967 | intron-variant | NACC2 | GRCh38.p7 | 9:136090377 | GCCCACAGCTGCCCC[-/CT]GACTCTAGGCAGTGC | 138151 |
rs142626219 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136031877 | CTGGCTCTGCATTCC[C/T]ACCTCCTCTAACTGT | 138151 |
rs142646916 | in-del | -/TTT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136068920 | GATTGAAAGAATACT[-/TTT]TTTTTTTTTTTTTAA | 138151 |
rs142663387 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136029375 | TCCTTGAGAGCTGTA[A/C]TGTCCCTCAATAAAG | 138151 |