| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs142723650 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | NACC2 | GRCh38.p7 | 9:136030047 | ACCTGCTTAATTTTC[G/T]TAATTTTAGTAGACA | 138151 |
| rs142724330 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NACC2 | GRCh38.p7 | 9:136068878 | CCATTAAATGTAAAT[A/G]ATCTAAATACACCCA | 138151 |
| rs142770266 | in-del | -/A | 0.0558544 | 0.157504 | intron-variant | NACC2 | GRCh38.p7 | 9:136089689 | GGGGACCCCAGCCCC[-/A]AACAGAGTGAGTCAT | 138151 |
| rs142780360 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007831 | GTACACGGCTGGGTG[C/G]GGTGGGGGGACTGGG | 138151 |
| rs142782445 | snp | A/G/T | 0.00199529 | 0.0315338 | intron-variant | NACC2 | GRCh38.p7 | 9:136080368 | GTTCTAGGAAAATCC[A/G/T]CCCAGCAGCCCACTG | 138151 |
| rs142787602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136075667 | ACCTGTGCTGATGCT[A/G]TCCTGAGCTCCCTGT | 138151 |
| rs142805270 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NACC2 | GRCh38.p7 | 9:136082923 | CCTCTCTACGCCTAG[G/T]ATTTTGTGCTGCCTG | 138151 |
| rs142998446 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136093252 | CTGGAAGAACCGCTC[A/G]GCACCAAGATCGTCA | 138151 |
| rs143032327 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NACC2 | GRCh38.p7 | 9:136020806 | CACATGGCCATGCTC[A/G]ATTGGCTTTTGACAA | 138151 |
| rs143094913 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NACC2 | GRCh38.p7 | 9:136086344 | GGTGGGGGTGCCTCT[A/G]TTTTCCTGCATCATC | 138151 |
| rs143123200 | snp | C/T | 0.030665 | 0.119967 | intron-variant | NACC2 | GRCh38.p7 | 9:136077291 | GCCAAGATTGCGCCA[C/T]TGCACTCCAGCCTGG | 138151 |
| rs143132047 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015960 | AACTGGACCCTCGCG[G/T]GGCGGGGGGACTGGC | 138151 |
| rs143148205 | snp | G/T | 0.370162 | 0.219229 | intron-variant | NACC2 | GRCh38.p7 | 9:136024350 | TGTGTGAGGACAGAG[G/T]GTGTGTGTGTGAGGA | 138151 |
| rs143155060 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | NACC2 | GRCh38.p7 | 9:136088266 | GGAACTGTACCACTG[A/C]CCACATCAGGCCCAG | 138151 |
| rs143168542 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136070081 | AAGAACTTTACAAGA[A/C]TTAAAATTACACAGT | 138151 |
| rs143236878 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136067775 | GGGAGGCGGAGGTTG[C/T]GGTGAGCCGAGATCG | 138151 |
| rs143237316 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007095 | TAGTTCTTTTTTTTG[C/T]CTGCTAAAAATAGTA | 138151 |
| rs143274115 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NACC2 | GRCh38.p7 | 9:136072351 | AGGAGTTTGAGATCA[A/G]AATGGCCAACACAGT | 138151 |
| rs143285248 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024547 | TGGACAGTGTGTGTG[A/T]GGACAGTGTGTGTAA | 138151 |
| rs143380205 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136069673 | ATAAAAGAAAGCAAG[C/G]GTTGTTTTACTTCAA | 138151 |
| rs143429869 | in-del | -/CCTACTAAACC | | | intron-variant | NACC2 | GRCh38.p7 | 9:136033471 | AACATGGTGAAACCC[-/CCTACTAAACC]CTACTAAACCTCTAC | 138151 |
| rs143468635 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136067566 | CGATGGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 138151 |
| rs143537747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136056034 | TTCCCTTTCCCATAC[A/G]GTGCAGGCTCCAGGA | 138151 |
| rs143556166 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136064739 | AAATTCATATGGAAA[C/T]GCAAGGGACCCAGGA | 138151 |
| rs143563094 | in-del | -/CTGT | 0.0221141 | 0.102801 | intron-variant | NACC2 | GRCh38.p7 | 9:136086817 | TCCCAGCAGCGGCTG[-/CTGT]CTGTGCCTGGCTCCT | 138151 |
| rs143588317 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136059971 | GGGCGCACGGGGAGC[C/T]GCCTCGGGGGACCTG | 138151 |
| rs143627408 | in-del | -/T | | | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016162 | TTAAGATTTTTTTTT[-/T]GACTGATTGGTGATG | 138151 |
| rs143653445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136057936 | CCCATTAGAGACGGC[A/G]ACTTCGCGGCACACT | 138151 |
| rs143655110 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136056640 | AGGCCCCCAGCTTCA[C/G]GGTCACAGAGGTACG | 138151 |
| rs143695971 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | NACC2 | GRCh38.p7 | 9:136029826 | GCCTGGAGCTTGCTC[A/G]CTCACACACCCCTTG | 138151 |
| rs143793428 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136097161 | TATGTACACCTTACC[A/G]CATTTAACGTTCACA | 138151 |
| rs143801089 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136057800 | CCTGGAGCAGCTGTG[A/G]CCTGATCATCACCAC | 138151 |
| rs143829835 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024249 | TGTGTGAGGACAGAG[G/T]GTGTGTGTGAGGACA | 138151 |
| rs143886952 | in-del | -/GGAGGGAA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136023082 | AGAGGGAGGGAGGAG[-/GGAGGGAA]GGAGGGAAGAGGGAG | 138151 |
| rs143917631 | in-del | -/GTCTGCA | 0.0287284 | 0.116357 | intron-variant | NACC2 | GRCh38.p7 | 9:136092266 | GACCCAGGGAGCTGG[-/GTCTGCA]GACACTCACCGCCGG | 138151 |
| rs143919572 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | NACC2 | GRCh38.p7 | 9:136074146 | GTCTCCACAAATAAT[C/T]TGTTAAAAAATTAGC | 138151 |
| rs143940034 | in-del | -/AC | 0.0236746 | 0.106192 | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014595 | CACCTGGCCTAGGGA[-/AC]ACACACTCTGAAGGG | 138151 |
| rs143941402 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136025211 | ACCGGCCTTGGAGAA[C/T]GTGGGCACGGGCGCT | 138151 |
| rs143962061 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NACC2 | GRCh38.p7 | 9:136080928 | GCCGCTCGAGTAGGT[C/T]GGGGGGACACAGGCC | 138151 |
| rs144006650 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136021905 | TAAACTTGGGGGACA[C/G]AGAATCATTTCCATT | 138151 |
| rs144092806 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136026876 | ATGGACAAGACGGTA[A/G]ATTAACCCAGCAAAG | 138151 |
| rs144101846 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | NACC2 | GRCh38.p7 | 9:136071038 | AGTTCAAGACCAGTC[C/T]GGCCAACACAGTGAA | 138151 |
| rs144102100 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136094762 | CCGCCCTGGCCCCGG[C/G]CCAGTCCTGCCCCGG | 138151 |
| rs144153703 | snp | A/G | 2.4829e-05 | 0.00352333 | synonymous-codon, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136011978 | GTCCGCGGCGATCAC[A/G]TTCATCTCGCTCTCC | 138151 |
| rs144258402 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136068622 | TATACGCTGTCCCCT[G/T]AACTGCTGTTATGCA | 138151 |
| rs144322602 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | NACC2 | GRCh38.p7 | 9:136032987 | CACACCACTGAACTC[C/T]AGCCTGGGCAACAGA | 138151 |
| rs144330473 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014327 | GTTGTTGTTTAGAGA[C/T]GGGGTCTTGCTCTGT | 138151 |
| rs144342264 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136076553 | GACTGCGGAGGGGAG[C/T]TGGTGTTCAATGGGT | 138151 |
| rs144392807 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010218 | ACCCTCTGTCCCCTA[C/T]CAGTGCCCATACCTC | 138151 |
| rs144398886 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136081525 | TAACAGAATTCCCTC[A/G]TGACGTTTCTTGGAA | 138151 |
| rs144407098 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136006569 | TTATTATTTTGTAAA[C/T]GTGAATTTTACAAAG | 138151 |
| rs144434032 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | NACC2 | GRCh38.p7 | 9:136060547 | ACACTGGGGCCGGGT[G/T]GGGGGTGCCACTCTG | 138151 |
| rs144469434 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136031462 | CGTGCTTCAGCCTCC[C/T]GAGCAGCTGGGATTA | 138151 |
| rs144481834 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136064265 | CTGCACTCCAGCCTG[A/G]GTGACAGAGTGAGGC | 138151 |
| rs144589097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136065488 | AGCCAGATGTGGTGG[C/T]GCACGCCAGTAGTCC | 138151 |
| rs144590966 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096918 | AGGACCCGTGGCCCT[C/T]CAGGGATGGGAATGA | 138151 |
| rs144615877 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | NACC2 | GRCh38.p7 | 9:136064015 | AACTGTAGGCCAGGC[A/G]TGGTAACTCAGGCCT | 138151 |
| rs144626715 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NACC2 | GRCh38.p7 | 9:136092350 | CACAGGTTCCCAAGA[C/T]CCCTCATCAGCCCCC | 138151 |
| rs144630488 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NACC2 | GRCh38.p7 | 9:136090340 | GACTCCCTCCAAGAC[C/T]GCCGCAGAAGAACCA | 138151 |
| rs144639006 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NACC2 | GRCh38.p7 | 9:136067049 | TGAGGTCGGGAGTTC[A/G]AGACCAGCCTCGGCA | 138151 |
| rs144689610 | in-del | -/AATA | | | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016200 | TGTTCAGAGCTCTCC[-/AATA]AATAAATAAATAAAT | 138151 |
| rs144705338 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | NACC2 | GRCh38.p7 | 9:136023369 | TCAGCTCTCGGAGAA[C/T]GTGGGATCCCCGAGT | 138151 |
| rs144799681 | snp | G/T | 0.148326 | 0.228391 | intron-variant | NACC2 | GRCh38.p7 | 9:136046574 | CACCTGATGGGGACC[G/T]AGACGGGGCCTGCCT | 138151 |
| rs144807871 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136017692 | AGCCTGGTAGGCTGC[C/T]AGCACAGCCACCCTG | 138151 |
| rs144810746 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136089675 | TCCCCATTCAGAATG[A/G]GGGACCCCAGCCCCA | 138151 |
| rs144894041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136032083 | CCGCCAGACTCCTGG[A/G]ATCCCACCGGCCTTT | 138151 |
| rs144942302 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136023119 | GGGAGGAGGGAGGGG[A/G]AGGAGGGAGGGAGGA | 138151 |
| rs144964240 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | NACC2 | GRCh38.p7 | 9:136079132 | TCACGTATGTCTGTG[A/C]GTCCCGTCCTTAACA | 138151 |
| rs144964330 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136033022 | GATTCCATCTCAAAA[A/C]AAAATAAGTTGGGCA | 138151 |
| rs145014448 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | NACC2 | GRCh38.p7 | 9:136066796 | CAATGTCATTCAGCA[A/G]TGATAGGAATGAAGT | 138151 |
| rs145014859 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136031665 | TTAAGACAAAGAAAA[A/C]AGAACAAGAAAACAC | 138151 |
| rs145029601 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | NACC2 | GRCh38.p7 | 9:136076868 | AAAAAAAATTAGCCG[C/G]GCGTGGTGGCGGGCG | 138151 |
| rs145036292 | snp | A/G | 0.185155 | 0.241444 | intron-variant | NACC2 | GRCh38.p7 | 9:136045397 | ACGGTAACCCTTTCC[A/G]AGCAGGGGACAGCTC | 138151 |
| rs145086010 | in-del | -/GAG | 0.11963 | 0.213316 | intron-variant | NACC2 | GRCh38.p7 | 9:136077643 | AACAGGCCCTTCACA[-/GAG]GAGAAGGTCCCCAGG | 138151 |
| rs145102796 | in-del | -/G | 0.00676609 | 0.0577691 | intron-variant | NACC2 | GRCh38.p7 | 9:136022107 | CCCTGCACTATCTCT[-/G]GCAGCTGCCGGCTTG | 138151 |
| rs145106079 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015802 | GGAGCTATGACGCCA[A/G]AGGAATCCAACACAA | 138151 |
| rs145220059 | snp | A/G | 0.000613298 | 0.0175007 | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016475 | GGCATCTGGGGGGCC[A/G]GGCTGCTCTGTGCCT | 138151 |
| rs145227448 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136006668 | ACGCTTGAAGCCCTC[A/G]GTTTCCCTGTTCGCT | 138151 |
| rs145265487 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | NACC2 | GRCh38.p7 | 9:136061940 | GCCTGGCCACCATGG[C/T]GAAATCCCATCCCTA | 138151 |
| rs145281981 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NACC2 | GRCh38.p7 | 9:136087972 | CCGGGAGGTGACCTG[A/G]GGACTCTGCTGGGAA | 138151 |
| rs145312777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136020454 | ACCATCAGAGACCAC[A/G]CAGGCAGCCCCACCA | 138151 |
| rs145316556 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NACC2 | GRCh38.p7 | 9:136091784 | GGCATATTTTACAAA[C/T]GATCTCATCTCACCA | 138151 |
| rs145351080 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NACC2 | GRCh38.p7 | 9:136066419 | CTCAGCATCATTAGC[C/T]GTCAGGGAAATCCAA | 138151 |
| rs145443330 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096962 | TTTTATTTTCTAAAT[A/G]TTAAAGACATTCTTC | 138151 |
| rs145477778 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | NACC2 | GRCh38.p7 | 9:136017971 | GCTTGCCGAGGGCAC[A/G]GCATGGTCCCCTCGG | 138151 |
| rs145582312 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136091380 | GTTCTCCCAGGAGAC[A/C]TGAGCCCAGGGTTCT | 138151 |
| rs145631701 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136075024 | TCACGAAACAGTGAC[A/G]TGAGGCCCAGTAGAG | 138151 |
| rs145646514 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NACC2 | GRCh38.p7 | 9:136064439 | ATAAAATCAAGTAAA[C/T]AATTCCATTTACAAC | 138151 |
| rs145877082 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NACC2 | GRCh38.p7 | 9:136078487 | AGCGCAGGAGAAATA[C/T]CATTACCCTACTGTA | 138151 |
| rs145923373 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136062487 | ATCTGGTAGCACTTC[A/G]TCTTCAGTGCCTAGG | 138151 |
| rs145984931 | snp | C/T | 5.15198e-05 | 0.00507516 | missense, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012007 | CCTTGAAGCTGGGGG[C/T]GAAGTTCTGACAGTA | 138151 |
| rs146037208 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136060063 | AGATGCCGGCTGCCC[A/G]CATCTGCCCTGGCGG | 138151 |
| rs146074020 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | NACC2 | GRCh38.p7 | 9:136030239 | AGTTTGCAGGCTGTA[A/C]AAAAACAGGACACGG | 138151 |
| rs146079614 | in-del | -/G | 0.25912 | 0.249834 | intron-variant | NACC2 | GRCh38.p7 | 9:136064191 | TACTCAGGAGGCTGA[-/G]AGGGGGGAGAATCAC | 138151 |
| rs146086352 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007726 | ACAGAGGGTTCTTGG[A/G]GTTTTCAGTTGGTTC | 138151 |
| rs146089445 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136056048 | CGGTGCAGGCTCCAG[A/G]AGGATTTGCTTTGAC | 138151 |
| rs146138823 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NACC2 | GRCh38.p7 | 9:136089178 | GGCAGCCACAGGCTA[C/T]CCCCGGGCCCCCACC | 138151 |
| rs146157065 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | NACC2 | GRCh38.p7 | 9:136086523 | AGCTTCCCGACAGCC[A/G]TCTGCCTGCCAGCAC | 138151 |
| rs146277575 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136074005 | TCCTTGACTATTTTT[G/T]TAAAAAAATTAAGAT | 138151 |
| rs146359201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136063612 | AAAAAGGCCGAGCAC[A/G]GTGGCTCACGCCTGT | 138151 |
| rs146384679 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009458 | TTGGTCCCCCTGGAC[A/G]TGGGCCCTGAGGAAT | 138151 |
| rs146578251 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | NACC2 | GRCh38.p7 | 9:136077127 | GAGGTTGCAGTGAGC[C/T]GAGATTGCGCCACTA | 138151 |
| rs146692835 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | NACC2 | GRCh38.p7 | 9:136069152 | ACCTTGTGATCTGCC[C/T]GCCTCGGCCTCCCAA | 138151 |
| rs146696749 | snp | C/T | 0.0763149 | 0.179815 | intron-variant | NACC2 | GRCh38.p7 | 9:136067083 | AACATGTCGAAACCC[C/T]GTCTCTACTAAAAAT | 138151 |
| rs146735292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136019509 | CTGTGAAGAAACTCA[A/G]GTGCCAGGACGGTGC | 138151 |
| rs146761497 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136024023 | GTGTGCCAGCTGTGA[A/G]TTCCTCTGGGAGACA | 138151 |
| rs146841501 | snp | G/T | 0.0119091 | 0.0762411 | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006419 | GGACGCCGCTAACAG[G/T]GACGGGGTCCTGAGG | 138151 |
| rs146860589 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NACC2 | GRCh38.p7 | 9:136061646 | CCCAGCCCCCAGCCT[C/T]AGCCCTCACACGGCC | 138151 |
| rs146931386 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NACC2 | GRCh38.p7 | 9:136028509 | GCCTCCTGCGTAACT[A/G]TGACTACAGGTGATG | 138151 |
| rs146979790 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NACC2 | GRCh38.p7 | 9:136083297 | CCTGAGCCTAGGCAC[A/G]CGGAGGTCATCTCCT | 138151 |
| rs146986006 | snp | C/T | 0.00993419 | 0.0697739 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008057 | CGCAGTCACCAACGC[C/T]GGCACCCCCAGGCGG | 138151 |
| rs146994018 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136080475 | TACTCGGGAGGCTGA[C/G]ACAGGAGAATTGCTT | 138151 |
| rs147037086 | snp | C/G | 0.0217236 | 0.101931 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011175 | CAGGAGGAGCAGGAA[C/G]GGCAGGGAGGAAGGG | 138151 |
| rs147098678 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136070151 | ACAAAGGTAACAGGG[A/G/T]AATCTAGAAATGGAA | 138151 |
| rs147154652 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136056742 | TGCAGGGCTGGGCCC[A/C]GGCCGGGCTCTCTCC | 138151 |
| rs147171392 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | NACC2 | GRCh38.p7 | 9:136037961 | TCCTTTAACCAGTGA[A/G]TGCGTACACAAATTG | 138151 |
| rs147240977 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | NACC2 | GRCh38.p7 | 9:136018185 | ACCTGGCCATGCTGT[A/C]CCTGTTCCCAGTCCC | 138151 |
| rs147261299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136093210 | GAAAGCAGGACTCCG[A/G]AGGCAGAGGCCAAGA | 138151 |
| rs147264094 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136022292 | CCCCACATGCAGTGG[G/T]CCTCGGGGAGATGAC | 138151 |
| rs147278505 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136090102 | CTCTGTTAAAGCTGA[C/T]TTTTTAACAGCACAA | 138151 |
| rs147365643 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136077742 | TGGCCACCCCCACAC[C/T]GGGGAGCAGGCAAGG | 138151 |
| rs147381915 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136076709 | GTGTATATTTGACTA[C/T]AATTTTTAAAAAATG | 138151 |
| rs147465198 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136093675 | TCCTCCCCTTGGACT[A/C]TGGCCCAGCTACCAC | 138151 |
| rs147470910 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136068077 | ATGAATGGAACTTGC[A/G]GGACTGGGCATTGCT | 138151 |
| rs147487728 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | NACC2 | GRCh38.p7 | 9:136066341 | TTAAAAATAGGCAAG[A/G]CATCTGAAAAGGTAT | 138151 |
| rs147503855 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | NACC2 | GRCh38.p7 | 9:136021556 | CTGCTTGGTGGCTTC[G/T]TGTCAAGTTCAACAT | 138151 |
| rs147574080 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | NACC2 | GRCh38.p7 | 9:136031800 | TGATCTCATCCCATA[C/G]AGCTAGTGGCCACTC | 138151 |
| rs147639511 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | NACC2 | GRCh38.p7 | 9:136090341 | ACTCCCTCCAAGACC[A/G]CCGCAGAAGAACCAA | 138151 |
| rs147679373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015631 | CAGGCTGTGGCCAAG[A/G]AAAGCGCCTGAGGGC | 138151 |
| rs147734110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136028885 | TGGCCAGGTGTATGT[A/G]CGCTCAGGGCAGTGC | 138151 |
| rs147814280 | in-del | -/AAAC | 0.0479149 | 0.147179 | intron-variant | NACC2 | GRCh38.p7 | 9:136077380 | ACATGGCCTTTGGCA[-/AAAC]AAACAAACAAACAAC | 138151 |
| rs147823523 | in-del | -/T | 0.0228947 | 0.104514 | intron-variant | NACC2 | GRCh38.p7 | 9:136028460 | AGCTCACTGCAACTC[-/T]TGCCTACTGGGTTCA | 138151 |
| rs147839541 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011251 | GAAGGGGGAGGGAAG[A/C]TACACTTGGAGGCTG | 138151 |
| rs147851028 | in-del | -/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136060897 | CAGGAAGCCCCCCAA[-/C]CACAGCCAGTCCCTG | 138151 |
| rs147884279 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136064222 | TGAGCCCAGGCGATC[A/G]AGGCTGCAGTGAACT | 138151 |
| rs147954078 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | NACC2 | GRCh38.p7 | 9:136072064 | CCAACATGGTGAAAC[C/T]CCGTCTGTACTAGAA | 138151 |
| rs148005007 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NACC2 | GRCh38.p7 | 9:136064989 | ATGTGGTGCTGGGAC[A/G]ACTGGATAGCCACAT | 138151 |
| rs148063324 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | NACC2 | GRCh38.p7 | 9:136076013 | CGCTTCTCAAAGCCC[C/T]GCATGAAGGTTACGT | 138151 |
| rs148114627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136029827 | CCTGGAGCTTGCTCG[C/T]TCACACACCCCTTGC | 138151 |
| rs148142440 | in-del | -/AC | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007537 | ACGCACAGACGTGCA[-/AC]CACACAGACACGCAC | 138151 |
| rs148160660 | in-del | -/C | 0.0263992 | 0.111815 | intron-variant | NACC2 | GRCh38.p7 | 9:136058004 | CATGCCATAAATAGT[-/C]GAGGCGAGGTAAGAC | 138151 |
| rs148166809 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136067575 | GGGCGCGGTGGCTCA[C/G/T]GCCTGTAATCCCAGC | 138151 |
| rs148220005 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NACC2 | GRCh38.p7 | 9:136088443 | CAGCAGCTGCCCCTG[A/G]GCCCCTGGAAGCTGC | 138151 |
| rs148236702 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | NACC2 | GRCh38.p7 | 9:136077293 | CAAGATTGCGCCATT[A/G]CACTCCAGCCTGGGC | 138151 |
| rs148273197 | snp | C/T | 0.031825 | 0.122064 | intron-variant | NACC2 | GRCh38.p7 | 9:136035332 | ACGTGACTCCTGTGA[C/T]GCACTGAGAAGGTTC | 138151 |
| rs148325313 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | NACC2 | GRCh38.p7 | 9:136072452 | TGAGAGGCTGAGGCA[C/T]AAGAATTGCTTGAAC | 138151 |
| rs148374200 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NACC2 | GRCh38.p7 | 9:136020844 | CCAGCCTTTGTCAAC[A/G]GAGGAGGCAGCAGCC | 138151 |
| rs148393527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136060662 | CATGCTTAGCCCCGT[C/T]GGGTCTCAAAGGTGC | 138151 |
| rs148431230 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | NACC2 | GRCh38.p7 | 9:136031542 | GGGGTTTCACTGTGT[C/T]GGCCAGGCTGGTCTC | 138151 |
| rs148472581 | snp | A/G | 0.000153988 | 0.00877327 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011894 | GCGGTACATCTCCAC[A/G]CCCTCCGGCAGCATG | 138151 |
| rs148547965 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136078570 | GGAACCGTACCTGGA[A/T]GCATAGACGGGACTC | 138151 |
| rs148553326 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | NACC2 | GRCh38.p7 | 9:136063818 | AACCCGAGAGGTGGA[A/G]GTTGCAGTGAGCCGA | 138151 |
| rs148604423 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NACC2 | GRCh38.p7 | 9:136081061 | CGGGCCCAGGGTCAC[A/G]GATCACGAACGGCTG | 138151 |
| rs148620238 | snp | C/G | 0.00478085 | 0.0486577 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009167 | TAAAGTGCAAATTTG[C/G]GTGTGGGGCAGATGA | 138151 |
| rs148681918 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136056657 | GTCACAGAGGTACGG[G/T]GGGTCTCTGGGATGA | 138151 |
| rs148685656 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | NACC2 | GRCh38.p7 | 9:136023575 | AAGCCTGGTCCTGGA[A/G]ACTCAAGAAGTCCCC | 138151 |
| rs148719586 | in-del | -/A | 0.110167 | 0.207236 | intron-variant | NACC2 | GRCh38.p7 | 9:136029865 | CCTGGCTCACCCTCA[-/A]GAGGTGTGGGATCCG | 138151 |
| rs148738045 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NACC2 | GRCh38.p7 | 9:136066056 | AAACTAGCCGGGTGT[A/G]GTGGTGGGTGCCTGT | 138151 |
| rs148761504 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014482 | TTAATTTTGATGAAG[C/T]CTCCCTATGTTGCCC | 138151 |
| rs148829954 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136097068 | TCTGTGTGCCTATAC[A/G]TATGTACACCAACAT | 138151 |
| rs148863961 | snp | C/T | 0.030665 | 0.119967 | intron-variant | NACC2 | GRCh38.p7 | 9:136064617 | TATTAAAGTCTTCCT[C/T]AATAATGTTAATTAA | 138151 |
| rs148880246 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | NACC2 | GRCh38.p7 | 9:136091677 | CCCAAACCGTAAACA[A/G]CAAACGCAGGAAGGC | 138151 |
| rs148916693 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136082899 | TGCTCATTTCCCACC[A/G]TGCATGGCCCTCTCT | 138151 |
| rs148963116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136074840 | CAGCCTCGGCGTCTA[C/T]ACCTCACACAGAGCG | 138151 |
| rs148985009 | in-del | -/G | 0.378372 | 0.214524 | intron-variant | NACC2 | GRCh38.p7 | 9:136021344 | CCCACCTCCCAGTGC[-/G]GGAAACGTAAAAACA | 138151 |
| rs149126392 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136062162 | CAGGACAGGACAGGA[C/T]AGGACAGGACAGGAA | 138151 |
| rs149176311 | snp | G/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136006693 | TTCGCTTTTGAATGT[G/T]TCAGTTTTAGTTATT | 138151 |
| rs149187611 | in-del | -/AA/CA | 0.584326 | 0.126918 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007535 | AGACGCACAGACGTG[-/AA/CA]CACACACAGACACGC | 138151 |
| rs149195026 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NACC2 | GRCh38.p7 | 9:136072210 | GCCATTGCACTCTAG[C/T]CTGGGCAACAAGAGT | 138151 |
| rs149238913 | snp | C/G | 0.000431287 | 0.0146785 | missense | NACC2 | GRCh38.p7 | 9:136011875 | CGGCGGAGCCCATGA[C/G]CGTGCGGTACATCTC | 138151 |
| rs149243179 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NACC2 | GRCh38.p7 | 9:136084874 | ACTCACATGCAGTCC[C/T]GGAAGCAGGCCTACA | 138151 |
| rs149279095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136060368 | CTTTAAGCCGGGGCC[A/G]TAAAAGGTAATTACC | 138151 |
| rs149335753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136055617 | AATTTCTGCAGGATC[A/G]CCACCAGCAAGGGGA | 138151 |
| rs149355918 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136070527 | GAAAATCAAATACAA[G/T]GAAAAGAAAAATACA | 138151 |
| rs149408609 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NACC2 | GRCh38.p7 | 9:136029778 | CTGCCCACCCCACTG[C/T]AGCCAGTGTGCCTGG | 138151 |
| rs149446745 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | NACC2 | GRCh38.p7 | 9:136063127 | TCTGGTTGTGGGCCA[A/G]GTCTGTCGATCTGTC | 138151 |
| rs149495917 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008348 | CAGGGCAGGAGAGGC[A/G]GCTAGATCCCAGGCC | 138151 |
| rs149543742 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | NACC2 | GRCh38.p7 | 9:136077287 | GTGAGCCAAGATTGC[A/G]CCATTGCACTCCAGC | 138151 |
| rs149612979 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136065771 | CTGGAGCCGTGATCA[C/T]GCCACTGTCCTCCAG | 138151 |
| rs149615636 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136093193 | CACTGCCCACAAACC[A/G]GGAAAGCAGGACTCC | 138151 |
| rs149668688 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NACC2 | GRCh38.p7 | 9:136071674 | GAGAATTAAGTGGGA[A/G]AAATCAGGCTACCTG | 138151 |
| rs149719036 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136019487 | GCCACCTTCACCCTC[A/G]ACAGCCCTGTGAAGA | 138151 |
| rs149724751 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136030987 | ACTTTAGACGGAGCC[A/G]ATGAACTTCCAGATA | 138151 |
| rs149760496 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | NACC2 | GRCh38.p7 | 9:136023030 | AGAGGGACATTCACA[A/T]CAGGAAGGAGGGAGG | 138151 |
| rs149765167 | snp | A/G | 8.31069e-05 | 0.00644566 | synonymous-codon, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016365 | GGCAGGTAGGGCCAC[A/G]AGGTCGCGGCGGATG | 138151 |
| rs149788615 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136082088 | CCATTCTCCAAAGAC[G/T]CTCCACCTGAACACG | 138151 |
| rs149807944 | snp | C/T | 0.0111196 | 0.0737302 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010395 | TGCCCGAGCGGAGTC[C/T]CCCGCTCCCCAGGTC | 138151 |
| rs149843310 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NACC2 | GRCh38.p7 | 9:136078246 | GGACCCCCACCCCCC[A/G]CAACCTTGTGGCCAG | 138151 |
| rs149932256 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NACC2 | GRCh38.p7 | 9:136074118 | AGAGACCAGGAGAGA[C/T]GGTAAGATTATAGTC | 138151 |
| rs149965872 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015700 | CCAGAAAATGGCCCA[A/G]TAGTCACCAAAGAAG | 138151 |
| rs150102788 | snp | C/G/T | 0.00398564 | 0.0444627 | intron-variant | NACC2 | GRCh38.p7 | 9:136084544 | AACTGGCCCAGACCC[C/G/T]GGAGTCAGGGTCACG | 138151 |
| rs150104701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012275 | CCAGCAGCCTTGGCC[A/G]TCCGCCAGCTGTGAG | 138151 |
| rs150158832 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136080237 | CCCCCAGCCTGTACA[A/G]CCTCATCCCAGCAGG | 138151 |
| rs150241294 | snp | G/T | 0.0475351 | 0.146656 | intron-variant | NACC2 | GRCh38.p7 | 9:136067672 | AAACCCTGTCTCTAC[G/T]GAAAATACAAAAATT | 138151 |
| rs150256253 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NACC2 | GRCh38.p7 | 9:136074811 | TCACCTGCGGGGCTC[A/G]GGGATGTATCACTCA | 138151 |
| rs150271697 | in-del | -/A | 0.207559 | 0.246371 | intron-variant | NACC2 | GRCh38.p7 | 9:136019246 | GACTTGTTCATGGCA[-/A]GAGACAGGACGGCTC | 138151 |
| rs150315783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136062673 | TAATCCCAACATTTT[A/G]GGAGGTCAGCGGGGG | 138151 |
| rs150369320 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NACC2 | GRCh38.p7 | 9:136059802 | CATGAGCATGTCACC[C/T]GGCTTCCCCAGCCCT | 138151 |
| rs150458921 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NACC2 | GRCh38.p7 | 9:136032289 | TGGAAAAGCAGTCAA[C/T]GCAACTAAGCACATT | 138151 |
| rs150483615 | in-del | -/CT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136064398 | TCACAAGTATTTCTC[-/CT]TACACTTGCAATGAA | 138151 |
| rs150487549 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | NACC2 | GRCh38.p7 | 9:136093087 | GCACAGACCTCAGAG[A/G]AAGGGGCACAAGGTG | 138151 |
| rs150517710 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | NACC2 | GRCh38.p7 | 9:136078068 | TGAGCCACCGCGTCC[A/G]GCCCAATCATACTTT | 138151 |
| rs150558167 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | NACC2 | GRCh38.p7 | 9:136030753 | TACAACCTGCGCCTC[C/T]CAGGTTCAAGCGATC | 138151 |
| rs150574701 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NACC2 | GRCh38.p7 | 9:136076244 | CGTTTCCCGGCCCTG[C/T]GGAACTCGAAGAAGT | 138151 |
| rs150610325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136070230 | AATCAAATACGGGCC[A/G]GGCGTGGTGGCTCAC | 138151 |
| rs150685853 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NACC2 | GRCh38.p7 | 9:136017313 | CCCATGGTGCCACCC[C/T]GAGGTCCCTGGGCAG | 138151 |
| rs150731093 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NACC2 | GRCh38.p7 | 9:136057159 | TGCCGGGGGTCTGGT[C/T]CAGGGGCCTGTGTGA | 138151 |
| rs150775172 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | NACC2 | GRCh38.p7 | 9:136081072 | TCACGGATCACGAAC[A/G]GCTGCGGGGAGAAGA | 138151 |
| rs150840253 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136087099 | TGGCCGTGTGAGGAC[A/G]GAGGCAGAGACTGGG | 138151 |
| rs150894510 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136081479 | GGTGCCCAGGAAGGC[A/G]GTGCCGGGCGTCCGC | 138151 |
| rs150963596 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136071354 | TTGAGACCAGCCTGG[C/T]CAACATGGTGAAACC | 138151 |
| rs150965817 | in-del | -/GGGGG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136082991 | CCGTGTTTTACGGCT[-/GGGGG]GTCATAACTTCTGCC | 138151 |
| rs150997105 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136018969 | TGTGCTTGGAACACC[C/T]GCCCCTCCCCAGCCC | 138151 |
| rs151013764 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NACC2 | GRCh38.p7 | 9:136068987 | TAATGGCACAATCTC[A/G]GCTCTGTCTCCCAGG | 138151 |
| rs151043451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136058276 | CTACAGGGCAGACAC[C/T]CGCAGCACCTCATGG | 138151 |
| rs151173295 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136027932 | AATGGAAACTCTCTA[G/T]CAAGTCTGAACAAAG | 138151 |
| rs151211222 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136066420 | TCAGCATCATTAGCC[A/G]TCAGGGAAATCCAAA | 138151 |
| rs151219276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136083055 | AGATTGATCTCCTGA[C/T]GACCGAGCACTTCAC | 138151 |
| rs151219465 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013544 | TGTCCTCAGGGACTC[C/T]GGGGACGTCTGAGGA | 138151 |
| rs151227217 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136094157 | GAAGGAACGCGCAGC[A/G]GAGAACACAGCTCAG | 138151 |
| rs151255833 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007325 | AAACCCTAAATGCTC[C/T]GGTGGTGACGTGCAC | 138151 |
| rs151256927 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136079529 | CACCCGCAGGCATGG[A/G]CACCCCATGGCCTGC | 138151 |
| rs151262042 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015069 | GGCCCGTCTCCTGCC[C/T]CACCACTCCCACAGG | 138151 |
| rs180754759 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008435 | AGGTGTGGAGATAAC[C/G]TAGCTCTGTAATAGA | 138151 |
| rs180901713 | snp | A/G/T | 0.00318978 | 0.0398085 | intron-variant | NACC2 | GRCh38.p7 | 9:136066833 | AGAGCACGGATGAGC[A/G/T]CTACGCTAAGCGAAA | 138151 |
| rs180923615 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136090987 | GGCCCAGGAGCTCGC[A/G]GCCGCCCATGGCCCT | 138151 |
| rs180943730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136029439 | GCATACCTCATTTTC[C/T]TGGATGCGGAACAAG | 138151 |
| rs180965533 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NACC2 | GRCh38.p7 | 9:136079927 | TGTTCCCCAAGGAAA[A/G]CTTTTGGAGCTGTTC | 138151 |
| rs181089758 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | NACC2 | GRCh38.p7 | 9:136090322 | AAAGGCAGGGCCAAC[A/G]CTGACTCCCTCCAAG | 138151 |
| rs181160695 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136028705 | TGCAGTTGCCCAGCT[C/G]TGGCTGCAGACCTGA | 138151 |
| rs181176060 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136066722 | CAATAGCCAAGAAGT[A/G]GAAATACACAAATGT | 138151 |
| rs181177597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136079366 | GGCTTCCAGGCAGGA[A/G]ACACTCCTACAAGCA | 138151 |
| rs181257885 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136018478 | CTCCTGAGAACCATG[C/T]GGGGTCTGAAACCAC | 138151 |
| rs181270107 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136071966 | CCAAAGGCCAGGCAC[A/G]GTGGCTCGAGTCCGT | 138151 |
| rs181283007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136024952 | TCAGGGTGCAATTTC[A/G]GAACTGTCCCTTGGA | 138151 |
| rs181284019 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | NACC2 | GRCh38.p7 | 9:136063011 | GCCTGTCTTCTTGTG[G/T]CTCCCCAAGAGAAGA | 138151 |
| rs181334548 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136057637 | AAGCCAGCGCCAGCT[C/T]CAGCGCAGGGCCCCC | 138151 |
| rs181642240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136032782 | TCATGCCTGTAATCC[A/G]CCACTTTGGGAGGCT | 138151 |
| rs181647913 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136068360 | AAAAATTAGTTGGGC[A/G]TAGTGGTGTGTGCCT | 138151 |
| rs181657212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136085167 | TTTTTTTTTTTTGGC[A/G]AGACTGAGTTTCGCT | 138151 |
| rs181705636 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136017441 | ATGCACCAGGTGCGC[A/G]GGGCCAAGGAAACAC | 138151 |
| rs181732280 | snp | C/T | 0.0463947 | 0.145069 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136095760 | GCAGTCGCGTCCGCA[C/T]GGTGCAGCCTCCGGG | 138151 |
| rs181748237 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136062321 | GCACCTTTGACCTGC[C/T]ATCTACCCGGACCCT | 138151 |
| rs181752503 | snp | C/T | 0.000327861 | 0.0127993 | missense | NACC2 | GRCh38.p7 | 9:136011743 | GGTCAACATTCACGG[C/T]GTCAGTTCTCAGAGC | 138151 |
| rs181767641 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | NACC2 | GRCh38.p7 | 9:136093872 | CTAGGCGCCCCTGCT[G/T]GGGGGTGCTACAGGC | 138151 |
| rs181904725 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010715 | GCAGAGGGCAGCGTG[C/T]GCTACATCAGCTGTG | 138151 |
| rs181905092 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136032432 | AAATTTCCTTAATCT[C/G]ATAAAATGTATCACA | 138151 |
| rs181913986 | snp | A/C/G | 0.00159649 | 0.0282165 | intron-variant | NACC2 | GRCh38.p7 | 9:136068002 | TCGAAACATAGTAAA[A/C/G]GTTCAGTAAAAATAT | 138151 |
| rs181920180 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136077006 | GCGAGACTCTGTCTC[A/G]AAAATAAATAAATAA | 138151 |
| rs181969795 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | NACC2 | GRCh38.p7 | 9:136024095 | AGTGAGGGCCAGAGT[C/G]TGTGTGTGTGTGGGT | 138151 |
| rs181997059 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136057188 | GACTGAGCCGAGCCC[C/T]GCGCTTATGGGGAAT | 138151 |
| rs182011867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136071298 | GCCTATAATCCCAGC[A/G]CTTTGGGAGGTCAAG | 138151 |
| rs182016963 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136076254 | CCCTGCGGAACTCGA[A/G]GAAGTGCTGTAACTA | 138151 |
| rs182018806 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136089361 | CCCTCCCCACAGCCA[A/C]CCCCCTTGCTAGAAA | 138151 |
| rs182018875 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NACC2 | GRCh38.p7 | 9:136030482 | AGGCATGGTGGCAGG[C/T]GCCTGTAGTCCCAGC | 138151 |
| rs182101539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136025287 | GTCCCCAGACCCTTT[A/G]AGGAGTGCTGCTTAC | 138151 |
| rs182245175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136020302 | CTGATTGGGTTCTGA[A/G]GTGCTCCACGTCCTC | 138151 |
| rs182255098 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136080421 | CTATTAAAAATACAA[A/G]ATTAGCTGGGCGTGG | 138151 |
| rs182258617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136059047 | GGGAAGGTGCTGGGT[C/T]AGGGGCAGGGGAGAA | 138151 |
| rs182260107 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NACC2 | GRCh38.p7 | 9:136073122 | AACAAAGGACTAATA[C/T]CTAGGCTACATAAAG | 138151 |
| rs182387542 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136084594 | AGAATACACCAGGCT[A/G]GAAGAGCCCAGAGAC | 138151 |
| rs182396169 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136063225 | TCCCGGGACCCCTGG[C/G]CTGGTCTCGGCCATG | 138151 |
| rs182498596 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136030921 | GCCCACCTCAGCCTC[A/G]CAGTGCTGGGATTAC | 138151 |
| rs182508552 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136067020 | CTTTGGGAGGTCAAG[A/G]CAGGCGGATCACCTG | 138151 |
| rs182511744 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136081340 | CACACCCCCAACCAA[C/G]ATGAAGCCAGCCACC | 138151 |
| rs182661325 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067395 | ATGTTCTAAAATTCA[C/G]GATGGTAATGGTTGC | 138151 |
| rs182790456 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NACC2 | GRCh38.p7 | 9:136022117 | ATCTCTGCAGCTGCC[A/G]GCTTGGCACAGACCA | 138151 |
| rs182801520 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136069836 | TGAAGCACAAACCAA[C/T]AGAACTAAAGACAAA | 138151 |
| rs182802830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136073995 | CTCCGTCATGTCCTT[A/G]ACTATTTTTTTAAAA | 138151 |
| rs182805233 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136027082 | AAAAATAGAAACAGC[C/T]GGTGTGGTGGCACAT | 138151 |
| rs182807570 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NACC2 | GRCh38.p7 | 9:136087157 | CCAGGACAGTGGCAG[C/T]CTTGGGAGCTGGAGG | 138151 |
| rs182815589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136064534 | GAAAGCTTCAAAATT[C/T]TGTTGAAAGAAATGA | 138151 |
| rs182818376 | snp | A/C/G/T | 0.00358938 | 0.0422398 | intron-variant | NACC2 | GRCh38.p7 | 9:136077661 | GAGAAGGTCCCCAGG[A/C/G/T]GGTGACACCTGAGCA | 138151 |
| rs182927693 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031137 | TTTGCCTATGACATT[A/T]TTTCAAAGGTTTAAG | 138151 |
| rs182949413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136082360 | GCCACGTGCTGAGCC[A/G]GCGGATGGGCCTCCG | 138151 |
| rs183069943 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013649 | TTGTGGGGGTTGCAT[C/G]CACAAGCCCGTTTGA | 138151 |
| rs183083474 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NACC2 | GRCh38.p7 | 9:136060938 | TACAGGGGTCCGGGG[A/G]AAGGTGAAAGGGGGA | 138151 |
| rs183089440 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | NACC2 | GRCh38.p7 | 9:136086445 | TGAGGTCCCAGGTCT[G/T]CGAGCGGCTGGGCTT | 138151 |
| rs183090176 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136026106 | GCACTTTGGGAGGAC[A/G]AGGTGGGCAGATCAC | 138151 |
| rs183115133 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136091570 | GAGTTCATGTCCCCA[A/C]ATGACAAGCAACCAA | 138151 |
| rs183155081 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | NACC2 | GRCh38.p7 | 9:136085640 | GGTACAGGCGGGTGG[C/T]GGGCAGCCCTCTGCC | 138151 |
| rs183385557 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013114 | AGGTGGCCGGGAGCA[A/C]CCCCGCGGCCCACCC | 138151 |
| rs183404829 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NACC2 | GRCh38.p7 | 9:136069142 | CAAACTCCTGACCTT[A/G]TGATCTGCCCGCCTC | 138151 |
| rs183424540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136091279 | AGCCTCCAGCTCCTC[A/G]GAGGAGGCAGAGGAT | 138151 |
| rs183427819 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067492 | ATTTTGTTGTTCTCT[G/T]AACACCGCAGGTGAT | 138151 |
| rs183519787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014632 | GTGGCCCTGGGTTTG[A/G]GAAACACTCATGTCT | 138151 |
| rs183533452 | snp | A/T | 0.0221141 | 0.102801 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096215 | GGGTCCTTGCAGGAG[A/T]ATGGAGTGATACCGC | 138151 |
| rs183693700 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136061603 | GTTGAGACCCTGTGC[A/G]GCTCACACCTGGACC | 138151 |
| rs183707556 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136074586 | CAATTAACACAGACG[C/G]ACAGGTCAAAACCAT | 138151 |
| rs183710785 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136092732 | AGTCAAGTTCCCAAA[C/T]GTGTTCGTTACACTG | 138151 |
| rs183761755 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | NACC2 | GRCh38.p7 | 9:136055460 | GCAGCCCAACAGGAG[A/G]AGCCCTTTTCCTGGG | 138151 |
| rs183837028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136031741 | ACATGGTGACACAAA[C/T]CCTAAAGAAGTTCTA | 138151 |
| rs183842061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067661 | CCAACATGGTGAAAC[C/T]CTGTCTCTACTGAAA | 138151 |
| rs183854860 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136083627 | CCGAGACTGGCACGA[A/G]ACGGGCATGAGCCCA | 138151 |
| rs183882420 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136022808 | CACAATTATAAGGCA[G/T]GCCATTCTCTCATGT | 138151 |
| rs183989786 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136079484 | GCTGTACAGGCTGGA[C/T]GCCAGCAGGTGGGGC | 138151 |
| rs184047300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136060537 | GGTCAGCTCCACACT[A/G]GGGCCGGGTGGGGGG | 138151 |
| rs184148199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136028953 | ATGTTGGGCACCGTC[A/G]AGCACAAGAGGGAGG | 138151 |
| rs184168409 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136066745 | ACAAATGTCTATCAC[A/G]GGCTGAATGGGTAAG | 138151 |
| rs184180533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136021655 | CAGCCTGCACAGGAA[C/T]GCTTATCCCGTCTCT | 138151 |
| rs184218893 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008855 | GCCTGGCCCGCCCGG[A/G]GCGCAGGGAGAGCTC | 138151 |
| rs184244984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067767 | TTGAACCCGGGAGGC[A/G]GAGGTTGCGGTGAGC | 138151 |
| rs184259216 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136028624 | GCTGGCAGGAGCCGG[C/G]AACAGGTAGAAATCT | 138151 |
| rs184261365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136066493 | CTATAATCAAAAAGA[C/T]AGAAAACAAAGGTTG | 138151 |
| rs184389645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136032310 | TAAGCACATTAGCAG[A/G]GCAGCAGAGGAAAAC | 138151 |
| rs184404818 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NACC2 | GRCh38.p7 | 9:136083840 | GCTGAGGGGACCCCC[A/G]GCCTGGCTGGGTTGA | 138151 |
| rs184623335 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136076370 | TACCACGACAAAAAT[C/G]AAATGAAATTCTGAT | 138151 |
| rs184719009 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008127 | GGGGCAAAGTACAAC[A/C]ACCAAATCCAATGCA | 138151 |
| rs184748988 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NACC2 | GRCh38.p7 | 9:136062610 | TTCACACCAGCCTCA[C/T]TTATCACTCTAAAAA | 138151 |
| rs184766376 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136057117 | TGCGTCCGATAGGGC[C/T]TTGTGGGGTGCCCGT | 138151 |
| rs184767764 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | NACC2 | GRCh38.p7 | 9:136094306 | GACCCGGCCTCGCGG[A/C]CTTCAGACCCACAGG | 138151 |
| rs184769354 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136070868 | AAATTAATTTTAGTA[C/T]CAGAAATGAAACAGG | 138151 |
| rs184841688 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007838 | GCTGGGTGGGGTGGG[A/G]GGACTGGGCCAGCGC | 138151 |
| rs184841870 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | NACC2 | GRCh38.p7 | 9:136031571 | TCGAACTCCTGAGCT[C/T]AAGTGATCCACCCGC | 138151 |
| rs184947951 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136055912 | GTGTGGGGATGGGGC[A/G]GGCCTGCTGTGCCAG | 138151 |
| rs184958068 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024313 | GTGAGGACAGAGGGT[G/T]TGTGTGAGGACAGAG | 138151 |
| rs184962335 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136088630 | CTGCCATCCCAACCA[C/T]GATGGCCTCATTGAG | 138151 |
| rs185016266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136025067 | TAGAATTTGGCATCT[C/T]GTGTATTGGAGAGAT | 138151 |
| rs185020580 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136063184 | GCCGCATTCCCATTA[C/T]GTGGCGGGGACCAGG | 138151 |
| rs185032615 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | NACC2 | GRCh38.p7 | 9:136076879 | GCCGGGCGTGGTGGC[A/G]GGCGCCTGTAGTCCC | 138151 |
| rs185043138 | snp | A/G | 0.235564 | 0.249583 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136095608 | CGGCGCAGAGGACGG[A/G]GCTCGGCGGCCGGGT | 138151 |
| rs185060994 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136070485 | GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC | 138151 |
| rs185179567 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136091132 | TGCCTCTTGTTCTCC[C/T]GGGAGACTCCATGGC | 138151 |
| rs185206604 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078536 | CTTGGAGGTGGGACG[C/T]GGCCCGCTCACTGGC | 138151 |
| rs185320783 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136024882 | GGCAGGGCCTAAAGG[C/T]GGCAGTGGCTGACAG | 138151 |
| rs185394421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136027581 | GACCAGAAAATCCAA[A/G]AAGGTTTGTAAATTA | 138151 |
| rs185409915 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NACC2 | GRCh38.p7 | 9:136077984 | TCACCATGTTAGCCA[A/G]GCTGGTCTCAAACTC | 138151 |
| rs185473471 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136019165 | CCCCGGCCCCCAGCT[A/C]ACCCTCTGCAGGAGC | 138151 |
| rs185521487 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136065657 | ACAAATAATAAAAAA[C/T]TAGCCAGGAGTGGTG | 138151 |
| rs185558461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136093321 | GGAAAACAAAGGGAG[A/G]ATTGAAGAATTTTTT | 138151 |
| rs185601428 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136085310 | GTGAACCACTGTGCC[C/T]GACCCAAAAAAATTT | 138151 |
| rs185740758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136062237 | AGCAACTAAGCAACA[C/T]GATGACTGCAAATAC | 138151 |
| rs185747676 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136081370 | CCGCTGGGCTCCCCA[A/T]GGCCCAGCCCCACCC | 138151 |
| rs185867625 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136023883 | TGAAGGGCAATGCAC[A/G]GGATGCCACCCACAC | 138151 |
| rs185878496 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NACC2 | GRCh38.p7 | 9:136075485 | GCTCCGTGTGAACCT[A/G]CCGTCTCCTACATCG | 138151 |
| rs185912061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013498 | GCTGAGAAGATGACC[A/G]GGTGATGGGGCTGCA | 138151 |
| rs186041097 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136030567 | GTGAGCCGAGACTGC[A/G]CCACTGCACTCCAGC | 138151 |
| rs186045851 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | NACC2 | GRCh38.p7 | 9:136037859 | GTAGGTTATATGGTT[A/T]AAAAAAAAATGAAAA | 138151 |
| rs186047087 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136067040 | CGGATCACCTGAGGT[C/T]GGGAGTTCGAGACCA | 138151 |
| rs186059168 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136080844 | CCGGCCTGTGCCCGG[C/T]GCAAACTCCAGCCAG | 138151 |
| rs186061859 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136085764 | AGTTTAATTACTTTA[A/T]CTTTTACCTTTTTTC | 138151 |
| rs186144624 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136020759 | TGGACAGACAGGTCA[A/G]TGGCACAGAATAGGA | 138151 |
| rs186146760 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NACC2 | GRCh38.p7 | 9:136059299 | AGAGCTAAGCAAGGG[A/G]CACAGCCATGCTTGG | 138151 |
| rs186154954 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | NACC2 | GRCh38.p7 | 9:136073132 | TAATATCTAGGCTAC[A/T]TAAAGAATTAATTGG | 138151 |
| rs186230856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136033149 | CCATTGCACTCCAGC[C/T]GGGGCAACAGAGTGA | 138151 |
| rs186356809 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136058560 | GACATAAACATGGGA[A/C]TGACAGACTCTAGGA | 138151 |
| rs186367997 | snp | A/G | 0.000264767 | 0.0115028 | missense | NACC2 | GRCh38.p7 | 9:136011829 | TGTGCCGCGGCAGGC[A/G]GGAACTCGGGGTCGA | 138151 |
| rs186375831 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136090347 | TCCAAGACCGCCGCA[A/G]AAGAACCAAGGAAGG | 138151 |
| rs186408997 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136068468 | CACACCATTGCACTC[C/T]GGCCTGGGCAACAAG | 138151 |
| rs186448144 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136068076 | CATGAATGGAACTTG[C/T]GGGACTGGGCATTGC | 138151 |
| rs186451860 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136084614 | AGCCCAGAGACACAG[A/C]AAGACTCAAACAGAC | 138151 |
| rs186578913 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | NACC2 | GRCh38.p7 | 9:136072203 | AGATCGTGCCATTGC[A/C]CTCTAGCCTGGGCAA | 138151 |
| rs186594020 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136032593 | GTGGTTATGAGCAGA[C/T]GACATGTCTGTATCC | 138151 |
| rs186595482 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010943 | CTGCACACACACGCA[C/T]ACACACACACTCGTG | 138151 |
| rs186674396 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136018068 | CAGCTGTGCAGAGGG[A/C]GGGGTGGGGTGGAAC | 138151 |
| rs186693815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136071377 | GTGAAACCCCGTCTC[C/T]ACTAAAGATATGAAA | 138151 |
| rs186783865 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136064935 | TAATTTAACAAGGGT[A/G]CCAAGACCATTCAAT | 138151 |
| rs186787764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136077768 | CAAGGGGGCAACAAA[A/G]TTGTGCTTAAAATTA | 138151 |
| rs186900955 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136057419 | TTGAGCCCCAGATCC[A/G]CCCTATGGCCCCACC | 138151 |
| rs186916179 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136061896 | AGGCCAAGGCGGGCG[C/G]ATCACCTGAGGTCAG | 138151 |
| rs186926138 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136074850 | GTCTACACCTCACAC[A/C]GAGCGGCAGGAAGCG | 138151 |
| rs186938073 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136092738 | GTTCCCAAATGTGTT[C/T]GTTACACTGGGGTCT | 138151 |
| rs187014591 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024108 | GTGTGTGTGTGTGTG[G/T]GTGAGGACAGAGGGT | 138151 |
| rs187054215 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136030336 | TACTGGAGGCCGGGC[A/G]CGGTGGCTCACGCCT | 138151 |
| rs187072298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136026427 | GAACACATAGGACTT[A/G]GGGAAAGCCTAACAT | 138151 |
| rs187079095 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136080008 | ATGGGGCTGCCTGGG[A/C]CAGGCCTGGGGCTGA | 138151 |
| rs187196536 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136063511 | CATGTCCATCACCAG[C/G]ACCAGGACGAGCCTT | 138151 |
| rs187200112 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | NACC2 | GRCh38.p7 | 9:136067063 | CGAGACCAGCCTCGG[C/T]AAGCAACATGTCGAA | 138151 |
| rs187205938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136022345 | GTCCCACCCCCGAAA[A/G]CACACAGGTGTGGAC | 138151 |
| rs187206507 | snp | C/G/T | 0.0232938 | 0.105441 | intron-variant | NACC2 | GRCh38.p7 | 9:136083361 | CCCAGGCTGGGTTGG[C/G/T]GGGGAGGCAGCCACA | 138151 |
| rs187217978 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096100 | CCCGGAAAGACCCAG[A/G]GACCCCTCCTCAGCT | 138151 |
| rs187226331 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136061004 | GCCATGGTTTGTTCT[A/G]CACCATCACAGGGTG | 138151 |
| rs187255201 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NACC2 | GRCh38.p7 | 9:136066852 | CGCTAAGCGAAACAT[C/T]ACGCTAAGTGTGAAA | 138151 |
| rs187352468 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136031682 | GAACAAGAAAACACA[C/G/T]AACTTTTCCTTAAAG | 138151 |
| rs187354022 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007871 | AACAGTTTCAGCTGT[C/T]GAATGAGGACAGGTC | 138151 |
| rs187363112 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NACC2 | GRCh38.p7 | 9:136067545 | AGAATGCACTTAAAC[A/G]ATGCTCGATGGGCCG | 138151 |
| rs187410112 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136025635 | AAAAAAAAACGCAGC[C/T]GGGCGCAGTGGCTCA | 138151 |
| rs187425394 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NACC2 | GRCh38.p7 | 9:136077036 | AATAAATAAAATAGC[C/T]GGGTGTGGTGGCGGG | 138151 |
| rs187571525 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136027324 | GAAAGAGATGTACCA[C/G]GTAAATATTAAACAA | 138151 |
| rs187609589 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136077200 | GCTGGGCGTGGTGGC[A/G]GGCGCCTGTAGTCCC | 138151 |
| rs187688036 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031447 | GGTTCGAGCAATTCT[C/T]GTGCTTCAGCCTCCC | 138151 |
| rs187701638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136082964 | GCCAGATATCAGGGC[A/G]AGGGGGAAGACGCCG | 138151 |
| rs187792134 | snp | A/C/T | 0.0059581 | 0.0542557 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014008 | GGCTCGTGGCCTTCC[A/C/T]GGGCCATAGGGTCCG | 138151 |
| rs187800763 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NACC2 | GRCh38.p7 | 9:136069420 | CGGGCGTGGTGGCAG[C/G]CACCTGTAATCTCAG | 138151 |
| rs187814467 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136086585 | GACCCACACGCTGTC[A/C]TTTCCAGGCCACTTC | 138151 |
| rs187823542 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024470 | TGTGTGAGGACAGAG[G/T]GTGCGTGTGAGGACA | 138151 |
| rs187985681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136079659 | TCCTGGGGCCCTGCC[A/G]TGGCCGGCACTCCCC | 138151 |
| rs187986086 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067400 | CTAAAATTCACGATG[C/G]TAATGGTTGCATAAC | 138151 |
| rs188046968 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136092665 | CAGGGACATGTGCTA[C/T]CAAGGTGAAGGTGGA | 138151 |
| rs188279015 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136016053 | GCCAATCAGGAATGC[A/G]ACCAGCCCAGGGGAT | 138151 |
| rs188280621 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NACC2 | GRCh38.p7 | 9:136056305 | AGATGAGATGCAGCA[A/G]CTCTGGGCCAGGGCC | 138151 |
| rs188292717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136031007 | ACTTCCAGATATACA[C/T]AACTTACCAAACCTG | 138151 |
| rs188325023 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | NACC2 | GRCh38.p7 | 9:136074006 | CCTTGACTATTTTTT[A/T]AAAAAAATTAAGATC | 138151 |
| rs188333959 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NACC2 | GRCh38.p7 | 9:136021710 | GCAGCCCGGATGTCC[C/T]GCAATGGGCATGCAG | 138151 |
| rs188354849 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136073587 | CACAATTGGTCTCGA[A/C]TGCCAAAGAGAACAG | 138151 |
| rs188403322 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | NACC2 | GRCh38.p7 | 9:136022882 | AACTGGGAAGGCAAA[A/C]CATCACCAATTACCA | 138151 |
| rs188412228 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009244 | GCCCCTGCTCCACCC[C/T]GCGGCTTCCTCCCAT | 138151 |
| rs188489907 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136055706 | TCTAATAAGAGGTTC[C/T]GGACCTCAGCAAATG | 138151 |
| rs188511893 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136087907 | TGCCCAAGGCCGGCC[A/G]TGGCCCAGGAAGGCC | 138151 |
| rs188626263 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136083633 | CTGGCACGAGACGGG[C/T]ATGAGCCCAGGGCAC | 138151 |
| rs188630350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136024883 | GCAGGGCCTAAAGGC[A/G]GCAGTGGCTGACAGA | 138151 |
| rs188635077 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136060543 | CTCCACACTGGGGCC[A/G]GGTGGGGGGTGCCAC | 138151 |
| rs188641698 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136076613 | TCTGCAAACAGAGGT[A/G]AGGGTTGACAGCCAT | 138151 |
| rs188649685 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136091553 | GGTGAGTGCCGGTCC[C/T]GGAGTTCATGTCCCC | 138151 |
| rs188762994 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015673 | GCTTCCTGGAAAACC[A/G]GGAAGAAATCCCCAG | 138151 |
| rs188780116 | snp | C/T | 0.0115144 | 0.0749975 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096671 | ACTTCCAAACCCGCC[C/T]CGCAGTCTACTGTGG | 138151 |
| rs188789136 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136069886 | CTTCAACAGCCTTCT[C/T]TAAACAAGGATAGAA | 138151 |
| rs188842335 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136066072 | GTGGTGGGTGCCTGT[A/T]ACCCCAGCTACTCGG | 138151 |
| rs188903690 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | NACC2 | GRCh38.p7 | 9:136032716 | AGCCCATCCAACATG[A/G]TGAAACCCCATCTCT | 138151 |
| rs188905566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136068093 | GGACTGGGCATTGCT[C/T]TGGGTGAGTGAGTAG | 138151 |
| rs188915674 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136085032 | AATGTGCATGCTTCA[G/T]TCCACTGAAAAAGCT | 138151 |
| rs188947995 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007007 | CCAAACATTCCATCC[A/G]AAGGATGGATGCTCT | 138151 |
| rs188983526 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136070486 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCG | 138151 |
| rs188991657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136029022 | ATAAGCAGGTTAATG[A/G]TGGCAGGAGGCAGAC | 138151 |
| rs189068704 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136028645 | GTAGAAATCTTGCCC[A/G]CTTCCAAGTTGGAGG | 138151 |
| rs189074624 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136066551 | GGGAATGCAAAATGT[G/T]AGGGCCACTTATGGA | 138151 |
| rs189085662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136078988 | GCCGCCGCCCCTCTC[C/T]GATTCCCTAACGGTT | 138151 |
| rs189106430 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136028403 | TTTTTTTGAGACAGG[G/T]TCTCTTTCTGTCACC | 138151 |
| rs189125609 | snp | A/G/T | 0.0126979 | 0.078662 | intron-variant | NACC2 | GRCh38.p7 | 9:136078019 | CCTCGTGATCCACCC[A/G/T]CCTCGGCCTCCCAAA | 138151 |
| rs189129633 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136093359 | ACCACTAGCCCCCTG[C/T]CCAGGGCAGAGCAGC | 138151 |
| rs189275779 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136088631 | TGCCATCCCAACCAC[G/T]ATGGCCTCATTGAGG | 138151 |
| rs189279420 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NACC2 | GRCh38.p7 | 9:136066832 | GAGAGCACGGATGAG[C/T]GCTACGCTAAGCGAA | 138151 |
| rs189338755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136084536 | ATCTGTCAAACTGGC[C/T]CAGACCCCGGAGTCA | 138151 |
| rs189479610 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136094690 | GACCGGGAGGGCGAG[A/G]CGCGGGCCCGGCTGG | 138151 |
| rs189538300 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | NACC2 | GRCh38.p7 | 9:136017366 | AGAGCCCCTCTAGAG[A/C]GTTCATGGAGGGCCA | 138151 |
| rs189540441 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | NACC2 | GRCh38.p7 | 9:136057161 | CCGGGGGTCTGGTCC[A/G]GGGGCCTGTGTGACT | 138151 |
| rs189546843 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136019603 | ATGGAGGTGAACAAC[C/T]GCGCCCCCACACAGG | 138151 |
| rs189547796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136070923 | TAGCAAAAGGATAAC[A/G]TGGAAATAGTAAGAA | 138151 |
| rs189558091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136088970 | AATGATCTCGGCATC[A/G]CGTGGAGCGGCTGAG | 138151 |
| rs189561132 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | NACC2 | GRCh38.p7 | 9:136058801 | CCCCCACCTGCACAC[A/T]TCGGGCAATGCCTCA | 138151 |
| rs189567742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136072529 | CAGCCTGCACAACAG[A/G]GCAAGACTCTGTCTC | 138151 |
| rs189606378 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067929 | CTATAAACCTATAGA[G/T]CATGTTACTGTACTG | 138151 |
| rs189633271 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008185 | TGGACAGACACAATG[C/T]GGAAAACAAGACAGA | 138151 |
| rs189654515 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136067692 | ATACAAAAATTAGCC[A/G]AGCGTGGTGGCGGGC | 138151 |
| rs189796320 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136023908 | CCACACAAGTGTGTA[C/T]CCACCGCCATACACA | 138151 |
| rs189883704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136063190 | TTCCCATTACGTGGC[A/G]GGGACCAGGGATGAG | 138151 |
| rs189896375 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NACC2 | GRCh38.p7 | 9:136038235 | GACTACATGACTATA[C/T]GTATTTTTTTAAACA | 138151 |
| rs189900599 | snp | C/T | 0.0528381 | 0.153711 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136095644 | AAGGACCTGGAGCGC[C/T]GCCCTCCGCCCTCCC | 138151 |
| rs189910015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136031766 | GTTCTAAAGAAAATA[C/T]TAGCAAATAAGAAAT | 138151 |
| rs190049892 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136062289 | CACCCAGCAGTCACT[C/T]GCTTACCTAGGAGGA | 138151 |
| rs190069681 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136093722 | GGGAAAACGCCAAGA[A/G]GCCTCTTTAAGGGAG | 138151 |
| rs190148203 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136057559 | TCTCCCTCACCCATA[G/T]TTGTAATTTAAATAA | 138151 |
| rs190164775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136090218 | CGAGGCAGATGCCCA[A/G]GGCCTGGGTGGGGGC | 138151 |
| rs190168410 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136026660 | AAATGACAAAGGCAC[A/G]TCTAGTGGTGCTTAC | 138151 |
| rs190173871 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136064454 | CAATTCCATTTACAA[C/T]GGCATCAAAAAGCAT | 138151 |
| rs190186563 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NACC2 | GRCh38.p7 | 9:136077279 | AGGTTGCAGTGAGCC[A/G]AGATTGCGCCATTGC | 138151 |
| rs190382683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136018341 | CCCAGAGTCACCTTT[A/G]CACCCAGCGCCTGTC | 138151 |
| rs190401754 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136071900 | GCAACTGAACGTCCA[C/G]ACGCAAATGTGCTGA | 138151 |
| rs190464875 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011017 | AGTCTCCGAAAGAAG[C/G]AAAAACGAGGAGTTA | 138151 |
| rs190528131 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136023070 | AGGAAGGAGGGAAGA[A/G]GGAGGGAGGAGGGAG | 138151 |
| rs190635576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136031036 | TGACACAAGAGGAAA[C/T]AGATTATGTGAACTA | 138151 |
| rs190782625 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136085962 | GGCACTGCACAGAAC[A/G]GCTCTGATGGGAGGG | 138151 |
| rs190804585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136030702 | AGTCTCGCTCTGTCA[C/T]CCAGGTTGGAGTGCA | 138151 |
| rs190808964 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | NACC2 | GRCh38.p7 | 9:136060472 | GCAGCAGGCGCTTCT[C/T]TCCAGAAGACAGGGC | 138151 |
| rs190820630 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067048 | CTGAGGTCGGGAGTT[C/T]GAGACCAGCCTCGGC | 138151 |
| rs190823291 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136073389 | GAGCTGTGGTCTTAC[C/T]GCTGCACTCCAGCCT | 138151 |
| rs190828903 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136081078 | ATCACGAACGGCTGC[A/G]GGGAGAAGAAACGCG | 138151 |
| rs190829705 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136091147 | CGGGAGACTCCATGG[C/T]GGCCTCCTCTTAAAG | 138151 |
| rs190894418 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067152 | CCGGCTACTCGGGAG[C/G]CTGAGGCAGGAGAAT | 138151 |
| rs191097644 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136068612 | AGCAACACTGTATAC[A/G]CTGTCCCCTGAACTG | 138151 |
| rs191183769 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136025266 | ACTGCAGACCTTCAC[A/G]CAACAGTCCCCAGAC | 138151 |
| rs191223629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136069264 | TAAAATGTATTCTAT[C/T]GACTGGGCGCGGTGG | 138151 |
| rs191274284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012332 | GGCTTCCGTAGCCCC[A/G]ACGGCTAACGGGAAC | 138151 |
| rs191289002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136022350 | ACCCCCGAAAGCACA[C/T]AGGTGTGGACTCAAC | 138151 |
| rs191308422 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136061602 | GGTTGAGACCCTGTG[C/T]GGCTCACACCTGGAC | 138151 |
| rs191324418 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | NACC2 | GRCh38.p7 | 9:136033409 | AGCACTTTGGGAGGC[C/T]GATGTGGGCGGATCA | 138151 |
| rs191325135 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136092711 | AGCAGAGTCAGGGGG[A/C]CCCATAGTCAAGTTC | 138151 |
| rs191348643 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | NACC2 | GRCh38.p7 | 9:136085503 | CAGAGCAAGACTCTC[A/C]AAAAAAAAAAAAGTT | 138151 |
| rs191421530 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136026065 | AAAGAATAGGCCAGG[C/T]GTGGTGGCTCACACC | 138151 |
| rs191437758 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | NACC2 | GRCh38.p7 | 9:136077053 | GGTGTGGTGGCGGGC[A/G]CCTGTAGTCCCAGCC | 138151 |
| rs191443169 | snp | C/G | 0.00366891 | 0.0426731 | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016460 | CAACCTGGTCAGATG[C/G]GCATCTGGGGGGCCG | 138151 |
| rs191457713 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136056467 | GGCCAGGCCCCTAGC[C/T]ATCATCCTTCCTGGG | 138151 |
| rs191465040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136070830 | GTTGACAAACATCTA[C/G]CAAGACTGACAAGAG | 138151 |
| rs191593011 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136091555 | TGAGTGCCGGTCCCG[G/T]AGTTCATGTCCCCAA | 138151 |
| rs191686574 | snp | A/C | 0.0322114 | 0.122752 | intron-variant | NACC2 | GRCh38.p7 | 9:136063902 | AAAAAAAAAAACAAA[A/C]AAAACAAAAATCACT | 138151 |
| rs191702715 | snp | A/G | 0.0221141 | 0.102801 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096214 | AGGGTCCTTGCAGGA[A/G]AATGGAGTGATACCG | 138151 |
| rs191882725 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136073820 | CAAGTACTGCATTTG[C/T]GTCCAAGCAGGATTT | 138151 |
| rs191885649 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | NACC2 | GRCh38.p7 | 9:136066909 | TATTATGAGATTCCA[A/T]TTATATAAAATGTCC | 138151 |
| rs191890413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136020933 | CCTCCGTCTCAGCCT[C/T]GCACCCTACACAAAA | 138151 |
| rs191930920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014397 | GTAGCCTCGACCTCC[C/T]GGGCTCCAGTGATCC | 138151 |
| rs191951312 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136069594 | AAAAAAAACACCTCA[A/C]TTCAAATATAATGAT | 138151 |
| rs191964820 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136086908 | CTTTCTGCCCCTCCC[A/C]CACCACACCGGGGGT | 138151 |
| rs192105880 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007944 | CCTCCCTACCTTCCG[A/C]CTTCCTCCTGGCTCT | 138151 |
| rs192112318 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136031696 | AGAACTTTTCCTTAA[A/G]GCAAAATTAGAGGGC | 138151 |
| rs192120280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067563 | GCTCGATGGGCCGGG[C/T]GCGGTGGCTCACGCC | 138151 |
| rs192124313 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136083394 | GAAGAGGGAGTGGGG[C/T]AGGTGGACACTTTGG | 138151 |
| rs192196036 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136080100 | GTCCCTACCCCGGGC[A/G]TGGCTGCCAGCCAAA | 138151 |
| rs192213670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136032216 | CATGTATAACAGAAG[A/G]CTGCCACAGCACAAC | 138151 |
| rs192328569 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136065564 | GGCAGAGGTTGTGGT[A/C/G]AGCCAAGATTGCGCC | 138151 |
| rs192364612 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136088673 | CCGGCCAGGAGGCAT[C/T]GTGGTCTGGGGTCAC | 138151 |
| rs192413702 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007396 | AGACACGCGTGCAGA[A/G]ACACGCACGTGCACA | 138151 |
| rs192429598 | snp | A/G | 0.021333 | 0.101051 | intron-variant | NACC2 | GRCh38.p7 | 9:136031559 | GCCAGGCTGGTCTCG[A/G]ACTCCTGAGCTCAAG | 138151 |
| rs192495682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136075345 | AAGCCCTCCCTAGCT[C/T]CCCCGAGGCTGGCTG | 138151 |
| rs192498945 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136092947 | AGAGAGGCAGCCTGG[A/G]GACAGTGTGTGGAGG | 138151 |
| rs192648864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015783 | CAGTTGTAAAAATCT[A/G]CAAGGAGCTATGACG | 138151 |
| rs192668331 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NACC2 | GRCh38.p7 | 9:136070463 | AGTGAGCCGAGATCG[C/T]GCCACTGCACTCCAG | 138151 |
| rs192715857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136027522 | AGGCTGAGTGCATTC[C/T]ATGTCCACTGGAAAT | 138151 |
| rs192760770 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NACC2 | GRCh38.p7 | 9:136083790 | CTGTTAGTGGTGGCA[C/T]GTTCCGGCCGCCCAC | 138151 |
| rs192841895 | snp | A/C/G | 0.0756104 | 0.179257 | intron-variant | NACC2 | GRCh38.p7 | 9:136028530 | ACAGGTGATGGCAGC[A/C/G]GTGGCCCGTCTGGAC | 138151 |
| rs192853301 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136078475 | ATCCTTAAAGTAAGC[A/G]CAGGAGAAATACCAT | 138151 |
| rs192888342 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NACC2 | GRCh38.p7 | 9:136055804 | GAGTCCCTCTACCCC[A/G]AGCCCCGGCCCCTGG | 138151 |
| rs192896096 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136088117 | CGGGCTTGTACGGTC[A/G]CCAGGTGGACAGTGG | 138151 |
| rs192965016 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067758 | GAGAATCACTTGAAC[C/T]CGGGAGGCGGAGGTT | 138151 |
| rs192999372 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136060712 | CTCCCAGGTGAAGAG[A/C]GTGAGAAACATAGCC | 138151 |
| rs193056824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136066392 | AATGTCCAATATACA[C/T]ACGCAAAAATACTCA | 138151 |
| rs193071094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067473 | AGAAATGCATCATTA[A/G]GTGATTTTGTTGTTC | 138151 |
| rs193074774 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136023779 | GGTTGAATCAATCCC[A/G]CCTATCACAGCACAT | 138151 |
| rs193202381 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136021771 | TGTTACCGCTTGGCT[A/G]TGAAAAGGAACAAAT | 138151 |
| rs193241832 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NACC2 | GRCh38.p7 | 9:136083086 | ACGGCAGAACCTTTC[C/T]GGCACCGCAACAGAA | 138151 |
| rs199561268 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136068210 | TTTTTAAAAAAGTAA[G/T]TGTGTGGCTGGGCGC | 138151 |
| rs199561711 | in-del | -/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136061895 | GAGGCCAAGGCGGGC[-/G]GATCACCTGAGGTCA | 138151 |
| rs199603200 | in-del | -/A | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096070 | CAAGGGCACGGAAAT[-/A]AAAACGGCCACACAC | 138151 |
| rs199608621 | in-del | -/AC | 0.0150606 | 0.0854603 | intron-variant | NACC2 | GRCh38.p7 | 9:136042684 | CAGACACACAGACAT[-/AC]ACACACAGACACACA | 138151 |
| rs199631130 | in-del | -/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136082664 | CTCCACGGACCTGCC[-/T]CCCAAGAAGCACCCC | 138151 |
| rs199689833 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136023059 | GGGAAGGAGGGAGGA[A/G]GGAGGGAAGAGGGAG | 138151 |
| rs199758836 | in-del | -/GAAA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074474 | AAAAAGAAAAAAGAA[-/GAAA]AAGAAAACAAAGTTC | 138151 |
| rs199880815 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074471 | AAAAAAAAGAAAAAA[C/T]AAGAAAAAGAAAACA | 138151 |
| rs200022708 | in-del | -/G | 0.0248432 | 0.108648 | intron-variant | NACC2 | GRCh38.p7 | 9:136032026 | GGCAGCACCCCTGGT[-/G]ATCACTGCCCAGGTT | 138151 |
| rs200110796 | snp | C/T | 0.000347939 | 0.0131852 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011464 | TGTTTGTATTAGTAA[C/T]GCATGCAAGCAGCTC | 138151 |
| rs200115582 | in-del | -/TAAAG | 0.0205511 | 0.0992634 | intron-variant | NACC2 | GRCh38.p7 | 9:136076077 | TCGAAAACTTGGAAA[-/TAAAG]TAAACAGGCACCCTT | 138151 |
| rs200119603 | in-del | -/TCAT | 0.0640965 | 0.167152 | intron-variant | NACC2 | GRCh38.p7 | 9:136031325 | CTTTACTCCACAGCC[-/TCAT]TCATTCATTCATTCA | 138151 |
| rs200120710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136073245 | CCAGCCTAGGCAACA[C/T]AGGGAGACTCTGTCT | 138151 |
| rs200168413 | snp | C/T | 1.71105e-05 | 0.00292489 | missense, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013219 | ACAGCGTTCAGGACC[C/T]GGCTGTCCAGCGGCT | 138151 |
| rs200181236 | in-del | -/G | 0.0611083 | 0.163768 | intron-variant | NACC2 | GRCh38.p7 | 9:136033102 | AATCACTTGAGCCCA[-/G]GAGGTGGAGACTGCA | 138151 |
| rs200241344 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136023117 | AGGGAGGAGGGAGGG[-/A]GGAGGAGGGAGGGAG | 138151 |
| rs200303683 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136070668 | CATCTCAAGGAATCA[A/G]AAAAAAAAAAAACAA | 138151 |
| rs200353628 | snp | A/C | | | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014994 | ATGTCCTGAAGGACA[A/C]GATGTCCAGGTGCGC | 138151 |
| rs200424009 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136035799 | TGAAAAACCTCTACA[A/T]GTAAAAAGAATGACA | 138151 |
| rs200428878 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074345 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 138151 |
| rs200462467 | in-del | -/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136063907 | AAAAAACAAAAAAAA[-/C]AAAAATCACTTAAAC | 138151 |
| rs200484680 | in-del | -/GGAA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136017807 | AGCTGCCTTCACTAG[-/GGAA]TCAATCCCACTGCCC | 138151 |
| rs200603351 | in-del | -/ACAG | 0.0267878 | 0.112589 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007489 | CAGACGCACACACGC[-/ACAG]ACACACACATGCACA | 138151 |
| rs200762626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136021344 | CCCACCTCCCAGTGC[A/G]GGAAACGTAAAAACA | 138151 |
| rs200789223 | in-del | -/GG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024207 | GTGTGTGAGGACAGA[-/GG]GTGTGTGTGTGTGAG | 138151 |
| rs200812799 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136069793 | ATCCTAAATGTCCAT[C/G]TACCAGACAACGGAA | 138151 |
| rs200840399 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136057576 | TGTAATTTAAATAAC[G/T]TAAGCTTGAAGAGCG | 138151 |
| rs200883203 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136089771 | CTATTTTCTTAAAAG[C/T]TTTTTTTTTTTCTTT | 138151 |
| rs200910441 | snp | A/C/G | 0.000926461 | 0.0215065 | missense, synonymous-codon | NACC2 | GRCh38.p7 | 9:136011744 | GTCAACATTCACGGC[A/C/G]TCAGTTCTCAGAGCC | 138151 |
| rs200945106 | in-del | -/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136023954 | CACACAAATGCACAA[-/C]CCCCCCCCACACACA | 138151 |
| rs200995189 | in-del | -/ACTCTG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031419 | CTCGGCTCACTGCAA[-/ACTCTG]CCTCCCGGGTTCGAG | 138151 |
| rs201082185 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136090870 | TCTCTGCAGCATGGC[A/G]TTGCCGTTCACCCCA | 138151 |
| rs201106932 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136075145 | GCGGCAGGCCAGGAA[C/G]TGGGGAGCCCCAGGT | 138151 |
| rs201139083 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136034635 | CGCCTGGAATGTTTT[A/G]CTGAAAGCAAGAAAA | 138151 |
| rs201142837 | in-del | -/C | 0.0236746 | 0.106192 | intron-variant | NACC2 | GRCh38.p7 | 9:136032034 | CCCTGGTGATCACTG[-/C]CCAGGTTTGACCACA | 138151 |
| rs201143571 | snp | C/T | 3.91144e-05 | 0.00442218 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136013973 | AGACCCCAGAGCCTG[C/T]AGCCACCAAACAGAA | 138151 |
| rs201177147 | in-del | -/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136022923 | CGCCACACCGTGCCT[-/G]TTAAGACACAGCCCG | 138151 |
| rs201203750 | snp | C/T | 0.000483582 | 0.0155421 | missense | NACC2 | GRCh38.p7 | 9:136011740 | TCAGGTCAACATTCA[C/T]GGCGTCAGTTCTCAG | 138151 |
| rs201244064 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074358 | CTCGGGAGGCTGAGG[C/G]AGGAGAATGGAGTGA | 138151 |
| rs201301524 | snp | A/C | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096633 | AGGTCCCACACCCCA[A/C]CCCCCCTCCCCCCAC | 138151 |
| rs201308280 | snp | A/G | 0.000844555 | 0.020532 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011702 | CTCCTCGCCGGCGTC[A/G]AAGGCGGGGTTGGCG | 138151 |
| rs201366112 | in-del | -/TG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024018 | GGGATGTGTGCCAGC[-/TG]TGAGTTCCTCTGGGA | 138151 |
| rs201390426 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136022925 | CCACACCGTGCCTGT[A/T]AAGACACAGCCCGTT | 138151 |
| rs201420540 | in-del | -/AAGAAGAAAAA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074469 | AAAAAAAAAAGAAAA[-/AAGAAGAAAAA]GAAAACAAAGTTCTT | 138151 |
| rs201501438 | in-del | -/A | 0.021333 | 0.101051 | intron-variant | NACC2 | GRCh38.p7 | 9:136060746 | GAGCACGGAGCCATC[-/A]GGGGGACCCTCAGAG | 138151 |
| rs201540990 | in-del | -/GGTA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024451 | TGTGTGAGGACAGAG[-/GGTA]TGTGTGAGGACAGAG | 138151 |
| rs201607376 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136084794 | CCCTGCAACCCGGAG[A/G]AGCCGTGGGGAGAGG | 138151 |
| rs201703395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136017246 | GTGCAGCGCGACCCC[A/G]ATGGCACCACGCGTC | 138151 |
| rs201754345 | in-del | -/ATGGCCAGGC | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074167 | AAAAATTAGCCAGGC[-/ATGGCCAGGC]GCGGTGGCTCATGCC | 138151 |
| rs201758739 | snp | C/T | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012674 | TTTTTTTTTTTTTTT[C/T]TTTTTTTTAGGAAGA | 138151 |
| rs201847833 | snp | C/T | 0.0030048 | 0.0386442 | missense | NACC2 | GRCh38.p7 | 9:136011701 | CCTCCTCGCCGGCGT[C/T]GAAGGCGGGGTTGGC | 138151 |
| rs201870181 | in-del | -/A | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136006813 | AAAGGCTTCCTCCTT[-/A]AAAAAAAAGACAAAA | 138151 |
| rs201966386 | snp | C/T | 0.187053 | 0.241946 | intron-variant | NACC2 | GRCh38.p7 | 9:136045396 | AGAGCTGTCCCCTGC[C/T]GGGAAAGGGTTACCG | 138151 |
| rs201972803 | in-del | -/ATG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074314 | AAAAATTAGCCGGGC[-/ATG]GTGGTGGGCGCCTGT | 138151 |
| rs202049171 | snp | G/T | 7.03594e-05 | 0.00593083 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013857 | CAGCACTCCTGCCCC[G/T]ACCTACCTGTCAAAG | 138151 |
| rs202068902 | in-del | -/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136090869 | ATCTCTGCAGCATGG[-/C]TTTGCCGTTCACCCC | 138151 |
| rs202149748 | in-del | -/G | 0.0193772 | 0.0965046 | intron-variant | NACC2 | GRCh38.p7 | 9:136032381 | ATGCAACACTTACGA[-/G]GAAAAAAAAAACCCT | 138151 |
| rs202211813 | snp | A/C | 0.261056 | 0.249755 | intron-variant | NACC2 | GRCh38.p7 | 9:136043424 | CTGATATTCCACCCA[A/C]GAGGAAGGGCTGAAA | 138151 |
| rs202227807 | snp | A/G | 0.00199801 | 0.0315438 | missense, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016346 | CGATCTGGCTGATGA[A/G]GCTGGCAGGTAGGGC | 138151 |
| rs367559509 | snp | C/T | 0.00119048 | 0.0243684 | missense | NACC2 | GRCh38.p7 | 9:136011632 | GGCTCTGGCCATCGG[C/T]GGGCAGCGGCTCGGG | 138151 |
| rs367637968 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136068720 | TGTCTCAATAAAGAT[A/G]TCATTTCAAAAATAA | 138151 |
| rs367644383 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074416 | CGAGGTTGTGCCACT[A/G]CACTCCAGCCCGGGC | 138151 |
| rs367758869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136090398 | CTAGGCAGTGCCCAG[A/G]AGTGAGAAGGTAACT | 138151 |
| rs367796125 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136067955 | TACTGAATAGCATAG[A/G]CAACTGTAACACAAT | 138151 |
| rs367930828 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136032394 | GAGGAAAAAAAAAAC[C/G]CTCTTAACCTAGGAA | 138151 |
| rs367965156 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136075998 | AAACTCCGAGACACC[C/T]GCTTCTCAAAGCCCT | 138151 |
| rs368006746 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136021273 | AAATTAGCACATGAA[A/G]AGACACTCAAGCATC | 138151 |
| rs368012198 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | NACC2 | GRCh38.p7 | 9:136034824 | GGGGGCCAGGCACAG[C/T]GGCTCATGCCTGTAA | 138151 |
| rs368014583 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009626 | GTAGAGGCGGCCCCA[C/T]GGGAGGTCTCCTAGG | 138151 |
| rs368024897 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031039 | CACAAGAGGAAATAG[A/G]TTATGTGAACTATTC | 138151 |
| rs368034978 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078369 | GGCAGGTTCTCCAAA[A/T]AATTCTGGCTCTCTC | 138151 |
| rs368053570 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136093734 | AGAGGCCTCTTTAAG[A/G]GAGGGGCTGGGAAAG | 138151 |
| rs368084532 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NACC2 | GRCh38.p7 | 9:136088660 | GGCCCCCACCCAGCC[A/G]GCCAGGAGGCATCGT | 138151 |
| rs368119183 | snp | C/T | 0.000203842 | 0.0100935 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011900 | CATCTCCACGCCCTC[C/T]GGCAGCATGGACTTG | 138151 |
| rs368136544 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136027568 | TAACAAAAAAGATGA[C/T]CAGAAAATCCAAAAA | 138151 |
| rs368228767 | snp | C/T | 0.000284981 | 0.0119335 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012039 | ACTGTGAGGACGGGG[C/T]GGCGTGAGCTCAGCC | 138151 |
| rs368259178 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136018496 | GGTCTGAAACCACCC[A/T]CCCTGGAGTCACCCT | 138151 |
| rs368320280 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136082359 | TGCCACGTGCTGAGC[C/T]GGCGGATGGGCCTCC | 138151 |
| rs368358989 | in-del | -/TTT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136085164 | TTTTTTTTTTTTTTG[-/TTT]GCGAGACTGAGTTTC | 138151 |
| rs368439258 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011156 | CCCTGCTTCGTCTTC[C/T]GGGCAGGAGGAGCAG | 138151 |
| rs368547500 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007822 | GCCCAGGCAGTACAC[A/G]GCTGGGTGGGGTGGG | 138151 |
| rs368564118 | in-del | -/CT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136060424 | ACAAACACCCAACTT[-/CT]ACAGCTCGGGAATGG | 138151 |
| rs368617797 | snp | G/T | 1.69827e-05 | 0.00291394 | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016230 | AAATAAATGAGGACA[G/T]TTGCATACAATAGAT | 138151 |
| rs368635269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136061485 | CCATGGCATTTGGCC[A/G]CAGGAAGGGGCTGGA | 138151 |
| rs368665247 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136018017 | GGGAAGTCCCCCGGT[C/G]GGGGGCGGGGGGCAG | 138151 |
| rs368672274 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136086085 | CCGACGGGCAGGAGC[C/T]GCCTCCAGGCCCTTC | 138151 |
| rs368687607 | snp | C/T | 4.07623e-05 | 0.00451436 | missense | NACC2 | GRCh38.p7 | 9:136011781 | GTGGCGGCGTCGCCC[C/T]GCCGCTCGGCGTAGA | 138151 |
| rs368710459 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136090562 | CCCTCAGCAGGCACC[C/T]AGCTCCCAACGCCCT | 138151 |
| rs368759413 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136092460 | CAGACGGGCTAGCGC[C/T]ACTTCTCTCCTGCCT | 138151 |
| rs368814974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136076883 | GGCGTGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT | 138151 |
| rs368837411 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136020781 | AGAATAGGAGACCCA[C/T]AGACAGACCCACATG | 138151 |
| rs368860808 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136090869 | ATCTCTGCAGCATGG[C/G]TTTGCCGTTCACCCC | 138151 |
| rs368882369 | snp | A/C | 0.00016072 | 0.00896293 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012046 | GGACGGGGCGGCGTG[A/C]GCTCAGCCACCTGCC | 138151 |
| rs368954254 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136087703 | TGTTTGCCCAGCTTC[C/T]ACCGCAGCACGGGGG | 138151 |
| rs369005252 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136086336 | GTTTGGGGGGTGGGG[A/G]TGCCTCTGTTTTCCT | 138151 |
| rs369052213 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136083948 | CAGTCAAAGCTGAGA[A/C]AGCCTCTCCGCCTCA | 138151 |
| rs369086792 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136076729 | TTTAAAAAATGTATT[A/G]GCCTGGTGGTGGCTC | 138151 |
| rs369095175 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136076962 | AGTGAGCCGAGATCG[C/T]GCCACTGCACTCCAG | 138151 |
| rs369099560 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136056323 | CTGGGCCAGGGCCCT[C/T]GGCGGCCAGGAACTC | 138151 |
| rs369104493 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136067450 | ATTAACGACGGGGAT[A/G]TATCCTGAGAAATGC | 138151 |
| rs369124718 | snp | C/T | 1.83296e-05 | 0.00302729 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013832 | CCCTCCGCAGCTCCA[C/T]TGTGCCCTCCAGCAC | 138151 |
| rs369136359 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078109 | AGGTTTGCCGTACTA[A/T]CTTTAAACAATCCAT | 138151 |
| rs369181243 | in-del | -/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136082196 | CTGAGGGATGCCCCC[-/T]CTGCCCGTCTCCCCA | 138151 |
| rs369219429 | snp | A/G | 3.64957e-05 | 0.00427159 | missense | NACC2 | GRCh38.p7 | 9:136011796 | CGCCGCTCGGCGTAG[A/G]TGCGTTGCTCGAACA | 138151 |
| rs369250148 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136028039 | CCAAGGTGGGTGGAT[C/T]ACTTGAGGTCAGAAG | 138151 |
| rs369266798 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013364 | TGGAGGCGACCCGCC[C/T]GCACGAATGCCCTGC | 138151 |
| rs369288682 | in-del | -/TGTG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024503 | TGTGTGAGGACAGAA[-/TGTG]TGTGTGTGTGTGTGT | 138151 |
| rs369293144 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010434 | AGCTCAGCTTCACAC[A/G]TACTAGTCGCCCACC | 138151 |
| rs369453396 | snp | C/T | | | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015526 | CACACCTGAGGCACT[C/T]GTCCTGCTGGGAGGG | 138151 |
| rs369457873 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136028425 | TCTGTCACCCATGCT[G/T]GAGTGCAGTGGTGCG | 138151 |
| rs369495886 | snp | C/G | 6.79013e-05 | 0.00582632 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013310 | TCCTGGTGGAGGGAC[C/G]GGAAAGGCAGGCAGG | 138151 |
| rs369520848 | snp | A/G | 3.39737e-05 | 0.00412137 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013311 | CCTGGTGGAGGGACC[A/G]GAAAGGCAGGCAGGG | 138151 |
| rs369541947 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136083778 | CCACCTCTCCACCTG[C/T]TAGTGGTGGCACGTT | 138151 |
| rs369560703 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136064644 | TTAAGGAATATGTCC[C/T]GAATTTATCTACAGA | 138151 |
| rs369568496 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136085435 | GAGGCGGGGAGATCA[C/T]CTGAGCCCGAGTTTG | 138151 |
| rs369574111 | snp | A/G | 0.000153988 | 0.00877327 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012075 | CCTGCCGGGAGGCCC[A/G]CCCCTCCCCAAGGCC | 138151 |
| rs369612531 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067352 | ATGAGAATGACTACT[A/G]AAGGGTGTGGTTTTT | 138151 |
| rs369624085 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136055990 | GGGGGCTGCTACCCC[A/G]TGGACCTTGCCCACC | 138151 |
| rs369634660 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024190 | TGTGAGGACGGAGTG[A/T]GTGTGTGTGAGGACA | 138151 |
| rs369686530 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136085165 | TTTTTTTTTTTTTTG[G/T]CGAGACTGAGTTTCG | 138151 |
| rs369708109 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136092887 | CGGAACCCACTGCGT[A/G]ACCCTGCAAAGGGGA | 138151 |
| rs369756002 | in-del | -/AATTA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136055662 | AATTAAATTAAATTA[-/AATTA]TCTTGCAGGATTTAA | 138151 |
| rs369766382 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078950 | AGATGCCCTTAGCAC[C/T]GTCGCCGGCATGATG | 138151 |
| rs369920810 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074436 | CCAGCCCGGGCGACA[A/G]AGCAAGACTCCGTCT | 138151 |
| rs369947295 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024423 | GTGTGTGTGTGTGAG[A/G]ACAGAGTGTGTGTGT | 138151 |
| rs369970881 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136071864 | GGAGAAGAGCCGGCC[G/T]TTGAAGCCAATGGAG | 138151 |
| rs370065758 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136090529 | TGTGGGGTGGGGGCT[A/G]GGTTGCTAGCAAGTC | 138151 |
| rs370069995 | snp | C/T | 0.000156941 | 0.00885696 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011828 | CTGTGCCGCGGCAGG[C/T]GGGAACTCGGGGTCG | 138151 |
| rs370072274 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136081317 | TAACCGGAACGACCT[A/G]CACACCACACACCCC | 138151 |
| rs370088069 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136080444 | GGGCGTGGTGGCGCA[C/T]GCCTGCAATCCCAGC | 138151 |
| rs370131635 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136067993 | ATTTGTGTATCGAAA[C/T]ATAGTAAAGGTTCAG | 138151 |
| rs370189464 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136018679 | GCACAGCCCCTGCCC[A/G]GCCACTACAGGGGTC | 138151 |
| rs370237187 | snp | A/G | 4.99297e-05 | 0.00499623 | missense, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016394 | TGAGGACGCAGGAGC[A/G]GCTCTCCAGCGGCAC | 138151 |
| rs370261079 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136062157 | CAGGACAGGACAGGA[A/C]AGGACAGGACAGGAC | 138151 |
| rs370308985 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136084844 | GTCACACGAGGACAC[C/G]CCCTGTGGGACTCCA | 138151 |
| rs370331292 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136058883 | GGGGACGCAGGGGCC[A/G]GGGCAGGATGGTCTC | 138151 |
| rs370414917 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136057832 | GGGGCCGGGGGTTGT[A/G]GAAGCGGTCGGATCC | 138151 |
| rs370495318 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136062987 | TACATGGCCTGTGCT[C/G]AACCCCATGCCTGTC | 138151 |
| rs370502522 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | NACC2 | GRCh38.p7 | 9:136083715 | GTGGCCTGGGGCTTT[G/T]GGCCTCCACCGCTGT | 138151 |
| rs370517161 | in-del | -/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136058113 | CTGGGGGCGGGGGGG[-/G]CCCAATGACGCCTGG | 138151 |
| rs370547554 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136029885 | GTGTGGGATCCGGGC[C/T]GGTAGTGCAAACCTG | 138151 |
| rs370548537 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136071004 | GGAGGCTGAGGTAGG[C/T]GGATCTCTTGAGGTC | 138151 |
| rs370606186 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136068919 | GAGATTGAAAGAATA[C/T]TTTTTTTTTTTTTTA | 138151 |
| rs370695059 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136077040 | AATAAAATAGCCGGG[C/T]GTGGTGGCGGGCGCC | 138151 |
| rs370706352 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074976 | CCCCCACTCACTGTC[A/G]CGTATGGGGCTGGGG | 138151 |
| rs370738262 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136084496 | GAGGCCACAGACAAA[C/G]CTACCTCGAGGGTCC | 138151 |
| rs370759738 | snp | C/T | 7.1945e-05 | 0.00599728 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136013997 | AACAGAAAAAGGGCT[C/T]GTGGCCTTCCCGGGC | 138151 |
| rs370786089 | snp | A/G | 1.66125e-05 | 0.00288201 | synonymous-codon, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016338 | GCGGTATCCGATCTG[A/G]CTGATGAGGCTGGCA | 138151 |
| rs370805684 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136017204 | CAGATGACGGCCAGG[C/T]GCCCTGCATCCTCAG | 138151 |
| rs370890324 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | NACC2 | GRCh38.p7 | 9:136018039 | GGGGGGCAGCTTGCA[A/G]GACCTGCTGGTCTCA | 138151 |
| rs370926252 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136020851 | TTGTCAACGGAGGAG[C/G]CAGCAGCCTTCACAA | 138151 |
| rs370932641 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136079149 | TCCCGTCCTTAACAA[G/T]AGAAAGCTTGAGCTC | 138151 |
| rs370934253 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136091453 | ACACTGGGGATGTGG[C/T]GGGGCCCCAGGAGCC | 138151 |
| rs370936392 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011104 | GGAAGGGTCAGTGAC[A/G]CACAGCCCAGCCCCC | 138151 |
| rs370938188 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136023333 | CATGACCCTGCAGCC[C/T]GCCAGGGCACCTGGG | 138151 |
| rs371007926 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136075637 | GGAGCAGAGCCTGCA[C/G]GGCCCCCTCAGGAAA | 138151 |
| rs371043563 | snp | A/C/T | 0.00285188 | 0.0376544 | missense | NACC2 | GRCh38.p7 | 9:136011550 | GTGCCCTCCGGCCTC[A/C/T]GGGCCGCGGCCGCCG | 138151 |
| rs371098224 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136025640 | AAAACGCAGCCGGGC[A/G]CAGTGGCTCATGCCT | 138151 |
| rs371116437 | in-del | -/ACAG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136042774 | CACACACAGAGACAC[-/ACAG]ACACACACACACATA | 138151 |
| rs371219779 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011305 | CCCTGGGAACTTCCT[C/T]GCAGGAGGCTGCCAG | 138151 |
| rs371243506 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136087225 | GAACCAGCCCTGAAG[A/C]TGCACAGAGTGTCAA | 138151 |
| rs371251905 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136076993 | CCTGGGCGACAGAGC[A/G]AGACTCTGTCTCAAA | 138151 |
| rs371275959 | snp | C/T | 1.71502e-05 | 0.00292827 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013336 | GCAGGGTGAGGATGA[C/T]GGGGAGGGTACCTGG | 138151 |
| rs371313320 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | NACC2 | GRCh38.p7 | 9:136085358 | TGGTGGTGCACAAAA[A/T]TTTTTTTTAAATCAG | 138151 |
| rs371324767 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136033372 | CTTCTGGCCGGGCAC[A/G]GTGGCTCACGCCTGT | 138151 |
| rs371351661 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136028470 | CAACTCTGCCTACTG[A/G]GTTCAAGCAATTTTT | 138151 |
| rs371424969 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136084155 | CCAGGAGGGGACCCG[C/T]CTTTCCAGGAGCAGT | 138151 |
| rs371520638 | snp | C/T | | | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015983 | GGACTGGCAACTATA[C/T]GTGACATGGTTTTAT | 138151 |
| rs371539423 | in-del | -/T | 0.0111196 | 0.0737302 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007086 | TTTTATACTTAGTTC[-/T]TTTTTTTGTCTGCTA | 138151 |
| rs371550693 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136037253 | TTTTTTGAGATGGAA[G/T]CTCACTCTTGCCCAG | 138151 |
| rs371591795 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136094032 | CAGGAGAGTGCGGCC[A/G]CGCTGGCGGGCGGGA | 138151 |
| rs371636029 | snp | C/T | 0.000422119 | 0.0145218 | missense | NACC2 | GRCh38.p7 | 9:136011821 | CGAACACCTGTGCCG[C/T]GGCAGGCGGGAACTC | 138151 |
| rs371667221 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031560 | CCAGGCTGGTCTCGA[A/C]CTCCTGAGCTCAAGT | 138151 |
| rs371687186 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136066844 | GAGCGCTACGCTAAG[C/T]GAAACATTACGCTAA | 138151 |
| rs371692340 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074422 | TGTGCCACTGCACTC[C/T]AGCCCGGGCGACAGA | 138151 |
| rs371743540 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012054 | CGGCGTGAGCTCAGC[C/T]ACCTGCCTGCCGGGA | 138151 |
| rs371773981 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074475 | AAAAGAAAAAAGAAG[-/A]AAAAGAAAACAAAGT | 138151 |
| rs371800379 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | NACC2 | GRCh38.p7 | 9:136093756 | CTGGGAAAGGCCCCA[C/G]AGAGGACCAGAGGGG | 138151 |
| rs371804370 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007197 | GGAATACGAGCCGGT[C/T]GTCCAGTCTGAATGC | 138151 |
| rs371829811 | in-del | -/CATA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136073131 | CTAATATCTAGGCTA[-/CATA]AAGAATTAATTGGCC | 138151 |
| rs371860236 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136092225 | GAACGAAATGCTGGG[C/G]AGAGGGCACTTCGGG | 138151 |
| rs371871870 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074445 | GCGACAGAGCAAGAC[C/T]CCGTCTCAAAAAAAA | 138151 |
| rs371915737 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136091864 | ACAACAACAAACAAA[A/C]AAACAGAGGTCACCA | 138151 |
| rs371917354 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024233 | GTGAGGACAGAGGGT[A/G]TGTGTGAGGACAGAG | 138151 |
| rs371919636 | snp | A/C | 0.000587159 | 0.0171241 | missense | NACC2 | GRCh38.p7 | 9:136011754 | ACGGCGTCAGTTCTC[A/C]GAGCCACGATGGTGG | 138151 |
| rs371921763 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136056155 | AGGCTGCCCAGCTCC[A/G]GATGTGCCAGGGCCT | 138151 |
| rs371939982 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136088612 | CCATCAGCAGGGGCT[G/T]CACTGCCATCCCAAC | 138151 |
| rs371958879 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136059169 | TAGCTGGGACATCTG[C/G]GGGCAAAACTGCCAC | 138151 |
| rs371991121 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136082424 | CTGTGAGAGGTCTGG[A/G]CAGGTGTGCACAGGG | 138151 |
| rs371993268 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136027679 | TTTATCTGAATGATA[A/T]TGAAAATCTGACATG | 138151 |
| rs372000174 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136021378 | ACGCCAAGTGCCGGC[A/G]AGGATGCGGGGCAGC | 138151 |
| rs372000175 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136090919 | TTTCAGGCCCCTCTG[C/T]TCCCCGCCCCCAGCC | 138151 |
| rs372014191 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136070395 | CGCCTATAATCCCAG[A/C]CACTGGGGAGGCTGA | 138151 |
| rs372014780 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136064896 | AGATGAGTCTACAAA[C/T]GTATTCATGTGTCTG | 138151 |
| rs372021525 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136022271 | CGGGTGATGAGGTAA[C/T]GGGTGCCCCACATGC | 138151 |
| rs372042034 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136076455 | GCACACACAGACAAC[A/G]CCACGGGGTTCCACT | 138151 |
| rs372089311 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074364 | AGGCTGAGGCAGGAG[A/G]ATGGAGTGAACCCGG | 138151 |
| rs372124678 | in-del | -/GAGTGTGTGTGTGTGTGTGAGGACG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024153 | GTGTGTGTGGGGACA[-/GAGTGTGTGTGTGTGTGTGAGGACG]GAGTGTGTGTGTGTG | 138151 |
| rs372250714 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NACC2 | GRCh38.p7 | 9:136067139 | CATGCCTGTAATCCC[A/G]GCTACTCGGGAGGCT | 138151 |
| rs372286891 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136093394 | CGAACCCTTCCAGCA[A/G]CCGGTGGTAAAGAAC | 138151 |
| rs372287644 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136088485 | GGTCAGTCAGCAGGA[C/T]GAGCCACTGCGCATG | 138151 |
| rs372452714 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | NACC2 | GRCh38.p7 | 9:136038495 | TAGTGAGTTGAGATC[A/G]TGCCACTGCATTCCA | 138151 |
| rs372536167 | snp | A/G | 0.000157988 | 0.00888644 | missense | NACC2 | GRCh38.p7 | 9:136011715 | TCGAAGGCGGGGTTG[A/G]CGGCGGCACTCAGGT | 138151 |
| rs372539528 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008714 | CTGAGCCCGGGCCGC[C/T]GCCCCCGCCCCACGG | 138151 |
| rs372579798 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136076887 | TGGTGGCGGGCGCCT[A/G]TAGTCCCAGCTACTT | 138151 |
| rs372586453 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136032635 | GGCCTGGTGGCTCAC[A/G]TAGGTAATCCCAGCA | 138151 |
| rs372616168 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136067506 | TGAACACCGCAGGTG[A/T]TTTTGTCGTTCTGTG | 138151 |
| rs372676988 | snp | A/C | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096933 | CCAGGGATGGGAATG[A/C]TTGTTTTAATCACTT | 138151 |
| rs372692346 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | NACC2 | GRCh38.p7 | 9:136023961 | AATGCACAACCCCCC[A/C]CACACACACGTGCAC | 138151 |
| rs372730442 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136022577 | GTCCATGGTCCCAGC[G/T]CGCTGCCTCCTGGCC | 138151 |
| rs372818779 | snp | C/T | 0.00033862 | 0.0130075 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012042 | GTGAGGACGGGGCGG[C/T]GTGAGCTCAGCCACC | 138151 |
| rs372848464 | snp | G/T | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096043 | TCCTGAGGACAGAGG[G/T]GCAGTTTTAAAACAA | 138151 |
| rs372891353 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NACC2 | GRCh38.p7 | 9:136086019 | CGCGCAGGGCAGCTC[C/T]GATGGGAGGGGTTGG | 138151 |
| rs372904249 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136071874 | CGGCCTTTGAAGCCA[A/G]TGGAGCTGGGGCAAC | 138151 |
| rs372940309 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136075264 | GGACACATTCTGGTC[C/G]AGTCCGGCACTGACC | 138151 |
| rs372945711 | in-del | -/TTTT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136079069 | AATCATAGCTTCTTC[-/TTTT]TTTTTTTTTTAAGTG | 138151 |
| rs372958421 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136017275 | TCAGAGACGGGCCCC[C/T]CGGAGGCTCCTGGGC | 138151 |
| rs373001530 | snp | A/G | | | intron-variant, upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136053353 | CGTGGAGGTGGCTTC[A/G]TGCCTAGTGTTTTCT | 138151 |
| rs373053577 | snp | C/G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078541 | AGGTGGGACGTGGCC[C/G/T]GCTCACTGGCCCTGG | 138151 |
| rs373073394 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136056653 | CAGGGTCACAGAGGT[A/G]CGGGGGGTCTCTGGG | 138151 |
| rs373119143 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136093279 | GTCACTGTTGTTTCA[C/T]GAATAATGCAGCCTC | 138151 |
| rs373243132 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136060934 | TGGGTACAGGGGTCC[A/G]GGGGAAGGTGAAAGG | 138151 |
| rs373315695 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136085166 | TTTTTTTTTTTTTGG[C/T]GAGACTGAGTTTCGC | 138151 |
| rs373434925 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136070538 | ACAATGAAAAGAAAA[A/C]TACAACATACCAAAG | 138151 |
| rs373445858 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136029921 | GCCTGCTGGGCCGAA[C/T]GGGTGGAATGAGCCC | 138151 |
| rs373447394 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136018187 | CTGGCCATGCTGTCC[C/T]TGTTCCCAGTCCCTC | 138151 |
| rs373493803 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136076963 | GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC | 138151 |
| rs373558694 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136055877 | AAGGTCAATCGAAGG[C/T]GCTCCTGGAGCGTGA | 138151 |
| rs373614816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136030089 | CATGATAGCCAGGCT[A/G]GTCTTGAACTCCTGA | 138151 |
| rs373620315 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136019640 | GCACCAGGGTCACGA[C/T]GAGAGGGCCCGGAGC | 138151 |
| rs373662995 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010360 | ACTCTCGCCCTGGCC[C/T]AGCCCTGGCCGCTGC | 138151 |
| rs373673385 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074297 | CTACTAATAAAATAC[-/A]AAAAAATTAGCCGGG | 138151 |
| rs373675906 | snp | A/C/G | 5.83856e-05 | 0.00540272 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011843 | CGGGAACTCGGGGTC[A/C/G]AGGGGCACGCTGGCG | 138151 |
| rs373684771 | snp | A/G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136029181 | CACTCATGGCTGCCC[A/G/T]TGGACAAATCAGCAT | 138151 |
| rs373702627 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136017749 | CCTCATTCCTGTGTC[C/G]CAGCACAAAAGGCAA | 138151 |
| rs373719720 | snp | C/T | 3.6901e-05 | 0.00429525 | missense | NACC2 | GRCh38.p7 | 9:136011799 | CGCTCGGCGTAGATG[C/T]GTTGCTCGAACACCT | 138151 |
| rs373753510 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024161 | TGGGGACAGAGTGTG[A/T]GTGTGTGTGTGTGTG | 138151 |
| rs373770922 | in-del | -/C | 0.00438332 | 0.0466095 | intron-variant | NACC2 | GRCh38.p7 | 9:136087875 | GGGAGGGCAAGCCCT[-/C]CCCGTCCCTTGTCTG | 138151 |
| rs373823003 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136058403 | CTCAGGGGTGTCCGG[C/T]GGAAGCAGCAGGCAC | 138151 |
| rs373855199 | snp | A/G | 0.000144113 | 0.00848739 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136013998 | ACAGAAAAAGGGCTC[A/G]TGGCCTTCCCGGGCC | 138151 |
| rs373909556 | in-del | -/GACA | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007358 | GCGTGCACACACACA[-/GACA]CACGCGTGCACACAT | 138151 |
| rs373960778 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136090321 | CAAAGGCAGGGCCAA[C/T]GCTGACTCCCTCCAA | 138151 |
| rs374008297 | snp | A/C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067633 | ACGAGGTCAAGAGAT[A/C/T]GAGACCATCTGGCCA | 138151 |
| rs374009705 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136087720 | CCGCAGCACGGGGGG[A/G]AATGAGGCTCGAATC | 138151 |
| rs374063401 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015667 | CTTGGGGCTTCCTGG[A/G]AAACCGGGAAGAAAT | 138151 |
| rs374065564 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074415 | CCGAGGTTGTGCCAC[C/T]GCACTCCAGCCCGGG | 138151 |
| rs374068338 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NACC2 | GRCh38.p7 | 9:136032379 | CAATGCAACACTTAC[C/G]AGGAAAAAAAAAACC | 138151 |
| rs374112287 | snp | A/G | 4.98393e-05 | 0.00499171 | synonymous-codon, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016344 | TCCGATCTGGCTGAT[A/G]AGGCTGGCAGGTAGG | 138151 |
| rs374130943 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136066899 | AGAGGGCACATATTA[C/T]GAGATTCCATTTATA | 138151 |
| rs374136855 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NACC2 | GRCh38.p7 | 9:136023629 | GATCCCAGCGATGAT[C/T]TTTATTGCTGATCTG | 138151 |
| rs374142120 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136068326 | AACATGGCAAAACCC[C/T]GTCTCTACCAAAAAA | 138151 |
| rs374163314 | in-del | -/AATA | 0.0115144 | 0.0749975 | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016199 | TGTTCAGAGCTCTCC[-/AATA]AATAAATAAATAAAT | 138151 |
| rs374188526 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136089515 | TGGGGGGCTCCTGTT[A/G]GCCCCTCCCCCAGCG | 138151 |
| rs374199854 | snp | C/T | 1.7081e-05 | 0.00292237 | synonymous-codon, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013887 | GAAGGTGGCCAGGAG[C/T]CTCCGCAGCAAGACC | 138151 |
| rs374306772 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136093094 | CCTCAGAGGAAGGGG[A/C]ACAAGGTGGAACCTT | 138151 |
| rs374326830 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136084330 | CCCCATGCACACCTG[C/G]GGCCTTCACCAAAGG | 138151 |
| rs374330158 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136071218 | ATCCAGCCTGGGAGA[C/G]AGAGCAAGACTACGT | 138151 |
| rs374380984 | snp | C/T | 7.27974e-05 | 0.0060327 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013839 | CAGCTCCATTGTGCC[C/T]TCCAGCACTCCTGCC | 138151 |
| rs374397833 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136077204 | GGCGTGGTGGCGGGC[A/G]CCTGTAGTCCCAGCC | 138151 |
| rs374423616 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014727 | CCTGGCTGGAGGGTA[C/T]GGCTGGAGCTTTGCA | 138151 |
| rs374441210 | in-del | A/GC | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096074 | GGGCACGGAAATAAA[A/GC]CGGCCACACACCCGG | 138151 |
| rs374470072 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067319 | CGGGAGCAGTGGGGG[G/T]GGGGGAGGGATGGGG | 138151 |
| rs374481610 | snp | A/G | 0.000993834 | 0.0222695 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011594 | GCTGGGGCCGCCCCC[A/G]CCCTGCTCAAAGGGC | 138151 |
| rs374498308 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136079848 | GTCTCAACTTTCCAG[A/G]ACCCCAAGGCCCCAG | 138151 |
| rs374503830 | snp | G/T | 0.000153988 | 0.00877328 | missense, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016405 | GAGCGGCTCTCCAGC[G/T]GCACTGGCTCAGGCT | 138151 |
| rs374604758 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136062862 | GCCGAGGCCGCAGTG[C/T]GCCGTGATCGTGCCA | 138151 |
| rs374608905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013580 | CTGTGTCCTCGGGAA[A/G]GGTTCTGTTGGCCCA | 138151 |
| rs374613499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136024818 | AACCCTGAGGGGCTG[C/T]GATCCTGAGAACTGG | 138151 |
| rs374636242 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136093532 | GAGCCCTGGGTGTGA[C/T]CACTGCGAAAGGATC | 138151 |
| rs374636348 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NACC2 | GRCh38.p7 | 9:136026419 | GACACATGGAACACA[C/T]AGGACTTGGGGAAAG | 138151 |
| rs374639559 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136059010 | TCCTGTCTGCAGGGA[A/G]AGGCAGTGTGGGGGC | 138151 |
| rs374646636 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136006607 | CAATTAATGATCACA[A/T]CCTTTTGTTTGTCAT | 138151 |
| rs374658951 | snp | A/C/G | 5.82082e-05 | 0.00539456 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011496 | AGTACTCGGTCCCTC[A/C/G]CGCAGCCACCCAGCT | 138151 |
| rs374676439 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136087550 | CTGGGGAAGGGCCCC[A/G]CAGCTTCTGGGGCCG | 138151 |
| rs374742031 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136084937 | CTGGGGCAAGGATGG[A/G]GAGTTTGTGTCTAAT | 138151 |
| rs374767905 | in-del | -/TG | 0.00517822 | 0.0506191 | intron-variant | NACC2 | GRCh38.p7 | 9:136061186 | ACCGTGAGCTCAGAC[-/TG]TGCCGGCTACCGGGG | 138151 |
| rs374811879 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136029609 | GGAGGTCCGTGAGCC[A/G]GGGCTGTGACACCTT | 138151 |
| rs374817927 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136092237 | GGGGAGAGGGCACTT[C/T]GGGGAAGGCCCAGGA | 138151 |
| rs374880013 | snp | C/T | 2.59939e-05 | 0.00360504 | synonymous-codon, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136011966 | GTTGGTGCACATGTC[C/T]GCGGCGATCACGTTC | 138151 |
| rs374882109 | in-del | -/C | 0.0158469 | 0.0875917 | intron-variant | NACC2 | GRCh38.p7 | 9:136058979 | GAGGCGTGACTCTGG[-/C]CCCTGGGCCCCGCCC | 138151 |
| rs374973105 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136086736 | CCCGTTTCCCTCCCA[C/T]GACCCCCGCTCAGCT | 138151 |
| rs374987310 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136090867 | GCATCTCTGCAGCAT[G/T]GCTTTGCCGTTCACC | 138151 |
| rs375032771 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136021105 | AAGCTAGCCACAGAC[C/T]GGAGGAAGATGCTTG | 138151 |
| rs375060163 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136022373 | GACTCAACACCCTCC[C/T]GCCCGATGCCCAGCA | 138151 |
| rs375064292 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010366 | GCCCTGGCCCAGCCC[C/T]GGCCGCTGCCTCCTG | 138151 |
| rs375095423 | in-del | -/CTT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136079058 | CAATCATAGCTTCTT[-/CTT]TTTTTTTTTTTTAAG | 138151 |
| rs375105093 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136077963 | CTTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 138151 |
| rs375170933 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136067304 | GTTGTTGCCTAGAGC[C/T]GGGAGCAGTGGGGGT | 138151 |
| rs375180565 | snp | C/G | 0.000153988 | 0.00877327 | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016476 | GCATCTGGGGGGCCG[C/G]GCTGCTCTGTGCCTG | 138151 |
| rs375193762 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012793 | CATCTGGGGCGCGGG[C/T]CGGGGGCGGCGGTCT | 138151 |
| rs375196105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136024056 | GTGTGTGGGGACAGC[A/G]TGTGTGTGTGAGGCC | 138151 |
| rs375220509 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136075652 | GGGCCCCCTCAGGAA[A/G]CCTGTGCTGATGCTG | 138151 |
| rs375254993 | in-del | -/AAAAAAAGAAAG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136066199 | CCCCATCTCAAAAAA[-/AAAAAAAGAAAG]AAAGAAAAAGAAACC | 138151 |
| rs375316402 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074378 | GAATGGAGTGAACCC[A/G]GGAGGCGGAGCTTGC | 138151 |
| rs375322155 | in-del | -/TATT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031345 | ATTCATTCATTCATT[-/TATT]CATTCATTCTGAGAT | 138151 |
| rs375342097 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136023363 | GCCTGCTCAGCTCTC[A/G]GAGAACGTGGGATCC | 138151 |
| rs375344385 | snp | A/G | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096172 | GTCCTCAGAGGCTAA[A/G]CCAGCCTCACTCCCA | 138151 |
| rs375345873 | snp | A/C | | | intron-variant, upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136051984 | CGCAGCTCAGCTGCA[A/C]CCAGGCCGGCCCTCC | 138151 |
| rs375385645 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136032383 | GCAACACTTACGAGG[-/A]AAAAAAAAACCCTCT | 138151 |
| rs375401401 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136018815 | TACACACCCCCACCC[C/G]CGGTGCAGCCTGCTG | 138151 |
| rs375421138 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136085023 | CAGCGCAAAAATGTG[C/T]ATGCTTCATTCCACT | 138151 |
| rs375433873 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015497 | CCAGCCCAGGCAACC[C/T]TCAGGCAGTGGCTCA | 138151 |
| rs375436694 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136084545 | ACTGGCCCAGACCCC[A/G]GAGTCAGGGTCACGA | 138151 |
| rs375468718 | in-del | -/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136092429 | TGCATCAGACGGCGG[-/G]CTCAGGTCCAGCGTC | 138151 |
| rs375471451 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136075170 | CCAGGTGTGGGTGCA[A/G]CAGGCTGCAACGCCC | 138151 |
| rs375473583 | in-del | -/TGTGTG | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136024173 | GTGTGTGTGTGTGTG[-/TGTGTG]AGGACGGAGTGTGTG | 138151 |
| rs375488431 | in-del | -/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136006912 | GAAAATTTATTTTTT[-/T]AACAGTCGTGAGTTA | 138151 |
| rs375507871 | snp | A/G | 0.00118927 | 0.0243561 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011720 | GGCGGGGTTGGCGGC[A/G]GCACTCAGGTCAACA | 138151 |
| rs375569462 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136058990 | CTGGCCCCTGGGCCC[C/T]GCCCTCCTGTCTGCA | 138151 |
| rs375578792 | snp | A/G | 0.000119144 | 0.00771737 | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016226 | AAATAAATAAATGAG[A/G]ACATTTGCATACAAT | 138151 |
| rs375612974 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136025705 | AGTCACTTGAGGTTA[C/G]GAGTTCGAGACAGCC | 138151 |
| rs375617609 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136032845 | ACATGGTGAAACCCC[A/G]TCTCTATTAAAAATA | 138151 |
| rs375620069 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | NACC2 | GRCh38.p7 | 9:136057871 | GACAGTCAGAGGTGG[A/G]CAATGGGAGGCGGTC | 138151 |
| rs375621673 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136073501 | ACAGGGGGTGTGAGC[A/G]TGGATCCAGCTGTAT | 138151 |
| rs375628768 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008960 | AGACGGCGATTACAA[A/G]CGAGTGAGGAAGGGG | 138151 |
| rs375648026 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136088515 | GGACATGGCCCAGTC[C/T]GTGGCCAGGGACTCT | 138151 |
| rs375649024 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136058437 | CTCAGGAGGGGGCTC[C/T]GGAGGCTCCCCAGGG | 138151 |
| rs375669294 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011009 | TGGCCCCGAGTCTCC[A/G]AAAGAAGGAAAAACG | 138151 |
| rs375780125 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136080813 | GCAGGGAGAGCAGAC[A/G]GCAGATGACCACAGG | 138151 |
| rs375824838 | snp | A/G | 1.7364e-05 | 0.00294647 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013346 | GATGATGGGGAGGGT[A/G]CCTGGAGGCGACCCG | 138151 |
| rs375836658 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136092040 | AACGAGATCCACCTG[A/G]GGATTAGGGGGCGCC | 138151 |
| rs375889911 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078802 | TGGTCCCCAGTAAGC[A/G]CCCCCAGCGTGGTCC | 138151 |
| rs375898119 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136065340 | AAATAAATAATTAGG[C/T]TGGGCGTGGTGGCTC | 138151 |
| rs375909972 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136022604 | GGCCAGTGAGCCTGT[C/T]CTGGGTCCAGTGCTT | 138151 |
| rs375911881 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136045196 | GGTGCCTGACCCCCA[G/T]GCCCTGCAGAGAGGC | 138151 |
| rs375916395 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136063901 | AAAAAAAAAAAACAA[A/C]AAAAACAAAAATCAC | 138151 |
| rs376063171 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136059993 | GGGGACCTGCAGGAG[A/G]CACAGGGCCGAGGGA | 138151 |
| rs376063836 | in-del | -/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136085164 | TTTTTTTTTTTTTTT[-/G]GCGAGACTGAGTTTC | 138151 |
| rs376075642 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136056919 | AATCCACAATTCCGT[G/T]TATCAGCCCTTCCTC | 138151 |
| rs376082371 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136079880 | GGCCAGGCCACAGCC[A/G]TGCTGTGGAAGGAGC | 138151 |
| rs376086348 | snp | A/G | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096475 | CCAACTTTAGGTTCT[A/G]TTCAGCTCTGCGTCC | 138151 |
| rs376139565 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136018417 | TCTGAGGACCCCACA[C/T]CCTGAATCCACAGCG | 138151 |
| rs376168251 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136081237 | AGGTGGACTCAGTCC[C/T]GACGGGCACTGGGGG | 138151 |
| rs376186611 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136071132 | CAGCTACTCGGGAGG[C/T]TGAGGCAGGAGAATC | 138151 |
| rs376189095 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136062120 | AACAGAGCGAGACAG[C/G]ACAGGACAGGACAGG | 138151 |
| rs376218340 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136084089 | GGTGGTGCTCGCTGA[A/G]GGTGTCCCTCACTCA | 138151 |
| rs376263540 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136071403 | TGAAAATTAGTTGAG[C/T]GTGGAGGCAGGTGCC | 138151 |
| rs376299919 | in-del | -/TC | 0.0236746 | 0.106192 | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006064 | GCCCACCTGCACTTG[-/TC]TCTCTGTTCACCTGG | 138151 |
| rs376326157 | in-del | -/CT | | | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006069 | CCTGCACTTGTCTCT[-/CT]GTTCACCTGGGGGCA | 138151 |
| rs376340850 | snp | A/G | 3.34717e-05 | 0.00409081 | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016250 | ATACAATAGATGGGT[A/G]GGAGGCAGCCTCACC | 138151 |
| rs376342687 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136033648 | AGCAAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 138151 |
| rs376347231 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136083689 | GAGGCAGGCGGGGGC[C/G]CCGAGACACTGTGGC | 138151 |
| rs376363425 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031634 | TGAGCCACTGTGCCC[A/G]GCCCACGGCCCCATT | 138151 |
| rs376454160 | in-del | -/GGACA | 0.239902 | 0.249796 | intron-variant | NACC2 | GRCh38.p7 | 9:136024533 | TGTGTGTGTGTGTGT[-/GGACA]GTGTGTGTGAGGACA | 138151 |
| rs376479362 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074447 | GACAGAGCAAGACTC[C/T]GTCTCAAAAAAAAAA | 138151 |
| rs376481808 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136068499 | AGTGAAACTCCGTCT[A/C]AAAAAAAAAAAAAAA | 138151 |
| rs376607254 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136019768 | GCCCGGGGCGCGGGG[C/T]TGGGGCCTTCAGGGA | 138151 |
| rs376624793 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136021491 | CGGGGCAGCTGGGAC[A/G]TCCTGACCTCACTGG | 138151 |
| rs376648504 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136093797 | TGGCCGGGAGAAGAA[-/A]GGGGTGGGTGGCTGA | 138151 |
| rs376720345 | snp | A/G | 0.000991042 | 0.0222382 | missense | NACC2 | GRCh38.p7 | 9:136011811 | ATGCGTTGCTCGAAC[A/G]CCTGTGCCGCGGCAG | 138151 |
| rs376746335 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136091471 | GGCCCCAGGAGCCCT[A/G]GGTCAGGGTCCCAAA | 138151 |
| rs376753531 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136089359 | CCCCCTCCCCACAGC[C/T]ACCCCCCTTGCTAGA | 138151 |
| rs376759098 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136060834 | TCCCTCCCACCAGAC[A/G]TGGCTATCCAGGGAT | 138151 |
| rs376817116 | in-del | -/CA | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007543 | AGACGTGCACACACA[-/CA]GACACGCACACACAC | 138151 |
| rs376848319 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136082407 | CTGCCTCCCCACCAT[A/G]CCTGTGAGAGGTCTG | 138151 |
| rs376853390 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136072578 | AAAAAAAGGCTGGGT[A/G]TGGTGGCTTATGCCT | 138151 |
| rs376853537 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009883 | GCACTTGTTTTGCAA[G/T]TGAAGATGGGGAAGC | 138151 |
| rs376940773 | snp | C/T | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136097067 | TTCTGTGTGCCTATA[C/T]GTATGTACACCAACA | 138151 |
| rs376979126 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136065925 | GAGGCCGGGCATGGT[A/G]GCTCACGCTTGTAAT | 138151 |
| rs376979711 | snp | A/G | 1.66355e-05 | 0.002884 | missense, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016382 | GGTCGCGGCGGATGA[A/G]GACGCAGGAGCGGCT | 138151 |
| rs377138089 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136017512 | CCACTTCCCTGTTGC[C/T]CCCCACCCCCACCAC | 138151 |
| rs377184452 | snp | A/G | 3.83502e-05 | 0.00437877 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012043 | TGAGGACGGGGCGGC[A/G]TGAGCTCAGCCACCT | 138151 |
| rs377190587 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074432 | CACTCCAGCCCGGGC[C/G]ACAGAGCAAGACTCC | 138151 |
| rs377191066 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136032311 | AAGCACATTAGCAGG[A/G]CAGCAGAGGAAAACC | 138151 |
| rs377195201 | snp | A/G/T | 0.0134861 | 0.0810011 | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014067 | GGGGGGAGGTGGAGG[A/G/T]GGAGGAGGAGCTGGA | 138151 |
| rs377208587 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136071995 | GTAATCCCAGCACTT[C/G]GGGAGGCCCAGGTGG | 138151 |
| rs377229780 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136092883 | ATCTCGGAACCCACT[G/T]CGTGACCCTGCAAAG | 138151 |
| rs377249114 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136094102 | ATGGGAGTCCGGGCT[A/G]CCTTGGGCACCCCCG | 138151 |
| rs377299219 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136028920 | ATGCCAGGCCCCTGC[C/T]GCCTTGGCCCCCTCT | 138151 |
| rs377302423 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136060513 | CCCCATCCCTCTCCC[C/T]TCCCTGAGGGTCAGC | 138151 |
| rs377306711 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074909 | AGGGCCGGGGGATGC[G/T]GGCGGGAATGGGTTC | 138151 |
| rs377344825 | in-del | -/AG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024205 | TGTGTGTGTGAGGAC[-/AG]AGTGTGTGTGTGTGA | 138151 |
| rs377361847 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136088852 | CCTACCCCAAGCCCC[A/G]AGGGGAGCCAGCCCA | 138151 |
| rs377383622 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136056383 | AGGATGGCGTGTGCC[A/G]TGTGCTCACCTCCCC | 138151 |
| rs377394262 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136084468 | CGTCCCTGCCCAAGA[C/G]GCCAATCACCAGGAG | 138151 |
| rs377428585 | in-del | -/AAAAC | | | intron-variant | NACC2 | GRCh38.p7 | 9:136069548 | GTGAAACTCTGTCAA[-/AAAAC]AAAACAAAACAAAAC | 138151 |
| rs377445619 | snp | A/C | 0.00493601 | 0.0494332 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014021 | CCCGGGCCATAGGGT[A/C]CGAAGAGGCGCACAG | 138151 |
| rs377501198 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136075530 | AAACAGATCGCGCAG[C/G]TGGGGCCAAGCCCAG | 138151 |
| rs377510894 | snp | A/G | 0.000256951 | 0.0113318 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011792 | GCCCCGCCGCTCGGC[A/G]TAGATGCGTTGCTCG | 138151 |
| rs377537078 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136091114 | AACCTCTGGAGAAAA[A/G]CCTGCCTCTTGTTCT | 138151 |
| rs377539016 | snp | C/T | 2.02517e-05 | 0.00318205 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011543 | TGCATAGGTGCCCTC[C/T]GGCCTCCGGGCCGCG | 138151 |
| rs377617408 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136070349 | CGTCTCTACTAAAAA[C/T]GCAAAAAAATTAGCC | 138151 |
| rs377618210 | snp | C/G | 0.144296 | 0.226554 | intron-variant | NACC2 | GRCh38.p7 | 9:136048876 | CCCCTCGGGGTCCAC[C/G]ACCTGCCCGTGGCTG | 138151 |
| rs377620515 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136078991 | GCCGCCCCTCTCCGA[G/T]TCCCTAACGGTTCCC | 138151 |
| rs377620677 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136060981 | ACCCCAGGATGCCCT[C/G]GCCTGAGGCCATGGT | 138151 |
| rs377620956 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011024 | GAAAGAAGGAAAAAC[A/G]AGGAGTTAGGCCCTG | 138151 |
| rs377621182 | snp | C/G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136023196 | GGATGGAAAGGGGCT[C/G/T]GCTGGTCTCTCGAGT | 138151 |
| rs377649244 | in-del | -/C | 0.00358779 | 0.0422022 | intron-variant | NACC2 | GRCh38.p7 | 9:136090199 | GGGAGATGGGCACAG[-/C]CCCCGAGGCAGATGC | 138151 |
| rs377690198 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136084223 | TGCAGCCTCCCCGCT[A/C]CCAGGTCAAAGACCT | 138151 |
| rs377753442 | snp | C/T | 7.06327e-05 | 0.00594234 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013856 | CCAGCACTCCTGCCC[C/T]GACCTACCTGTCAAA | 138151 |
| rs386416446 | in-del | -/CA | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007536 | GACGCACAGACGTGC[-/CA]ACACACAGACACGCA | 138151 |
| rs386739527 | in-del | ACACA/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010944 | TGCACACACACGCAC[ACACA/G]CACACTCGTGCACAC | 138151 |
| rs386739528 | multinucleotide-polymorphism | CA/TG | | | missense | NACC2 | GRCh38.p7 | 9:136011824 | ACACCTGTGCCGCGG[CA/TG]GGCGGGAACTCGGGG | 138151 |
| rs386739529 | multinucleotide-polymorphism | CA/TG | | | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014298 | CCTCAGCTCCCTCCC[CA/TG]AGAACACACTTTGTT | 138151 |
| rs386739530 | in-del | A/GTGTGTG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024164 | GGACAGAGTGTGTGT[A/GTGTGTG]TGTGTGTGAGGACGG | 138151 |
| rs386739531 | in-del | AGT/TGTGTGAGG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024173 | GTGTGTGTGTGTGTG[AGT/TGTGTGAGG]ACGGAGTGTGTGTGT | 138151 |
| rs386739532 | multinucleotide-polymorphism | CGC/TGG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031934 | CACAGCTGATGTGTA[CGC/TGG]GCAGCTGTTAACAGC | 138151 |
| rs386739533 | multinucleotide-polymorphism | AAT/GAC | | | intron-variant | NACC2 | GRCh38.p7 | 9:136063057 | TCACTGTTTTCTTCT[AAT/GAC]TTTTGTTCTCGTTGT | 138151 |
| rs386739534 | multinucleotide-polymorphism | CA/TG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136066493 | CTATAATCAAAAAGA[CA/TG]GAAAACAAAGGTTGG | 138151 |
| rs386739535 | multinucleotide-polymorphism | CA/TG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136068318 | GCCTGGTCAACATGG[CA/TG]AAACCCTGTCTCTAC | 138151 |
| rs386739536 | multinucleotide-polymorphism | AA/TC | | | intron-variant | NACC2 | GRCh38.p7 | 9:136070203 | CATATGTCAAAGAAG[AA/TC]GTCTCAAGAAAATCA | 138151 |
| rs386739537 | multinucleotide-polymorphism | ATCGCTTGAACCTGGGAGGCAGACGTTGC/GTCGCTTGAACCTGGGAGGCAGACGTTGT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136071145 | GGTTGAGGCAGGAGA[lengthTooLong]GGTGAGCCAAGATCA | 138151 |
| rs386739538 | in-del | AAGAAAAGAAAACAGTTCGGGCA/TTAGCCAGGCATGGCCAGGCG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074157 | TAATTTGTTAAAAAA[lengthTooLong]CGGTGGCTCATGCCT | 138151 |
| rs386739539 | multinucleotide-polymorphism | CA/TG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074225 | GGAGGCCGAGGAGGG[CA/TG]GATCACGAGGTCAGG | 138151 |
| rs386739540 | multinucleotide-polymorphism | CA/TG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074321 | AGCCGGGCATGGTGG[CA/TG]GGCGCCTGTAGTCCC | 138151 |
| rs386739541 | in-del | CCA/TC | | | intron-variant | NACC2 | GRCh38.p7 | 9:136082664 | CTCCACGGACCTGCC[CCA/TC]CCAAGAAGCACCCCT | 138151 |
| rs397705028 | in-del | -/CT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136064399 | CACAAGTATTTCTCT[-/CT]ACACTTGCAATGAAC | 138151 |
| rs397768743 | in-del | -/G | 0.375 | 0.216506 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009848 | TGCACACCGGAGGGG[-/G]TGCTGATGGGCGCAG | 138151 |
| rs397789617 | in-del | -/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136089782 | AAGCTTTTTTTTTTT[-/T]CTTTTTTATTAAAAA | 138151 |
| rs397800783 | in-del | -/CA | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007413 | ACGCACGTGCACACA[-/CA]GACGCGCGTGCACAC | 138151 |
| rs397803392 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136068518 | AAAAAAAAAAAAAAA[-/A]GTAATTGTGCAATGA | 138151 |
| rs397804921 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136073657 | GAATGTTTGCAGAAA[-/A]GTCGACTTGATTTCC | 138151 |
| rs397819370 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136091842 | TGCTTAAAAAAAAAA[-/A]CCAACAACAACAACA | 138151 |
| rs397960076 | in-del | -/AAA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136065823 | TCCAAAAAAAAAAAA[-/AAA]GAAAAGGAAAGAAAA | 138151 |
| rs398012572 | in-del | -/T | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136079072 | TCTTTTTTTTTTTTT[-/T]AAGTGCACACGGTAT | 138151 |
| rs398069062 | in-del | -/AA | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136006834 | AAAGACAAAAAAAAA[-/AA]GCTAAGCATCTGTGG | 138151 |
| rs398069063 | in-del | -/AATC | | | intron-variant | NACC2 | GRCh38.p7 | 9:136017813 | CTTCACTAGGGAATC[-/AATC]CCACTGCCCTGGGCT | 138151 |
| rs527299249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136039073 | ATCCCAACCATATGC[C/T]GTCTCTAAAAAATAC | 138151 |
| rs527391062 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136019320 | GTCGGGGCCAGAGCT[A/G]GGTTCCAGGGTGGCA | 138151 |
| rs527398916 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136077699 | GCTGTGTGGTCACCC[G/T]GGAAATGCGAGGGGA | 138151 |
| rs527403056 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136082496 | GTGTGTGCAGGGCGG[A/C]GCTGACAGTGGCCCT | 138151 |
| rs527418786 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136030079 | GGAGTTTCACCATGA[C/T]AGCCAGGCTGGTCTT | 138151 |
| rs527421615 | in-del | -/AA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136068500 | TGAAACTCCGTCTCA[-/AA]AAAAAAAAAAAAAAA | 138151 |
| rs527433282 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136077367 | AAGCAGAAGAGAAAC[A/G]TGGCCTTTGGCAAAA | 138151 |
| rs527443402 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136059563 | CGAAGTCGGCTAGAC[A/G]TTAAACAAAAGGCAA | 138151 |
| rs527506771 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136024569 | TGTGTGTAAGGACAG[A/T]GTGTGTGTGTAAGGA | 138151 |
| rs527508125 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136076477 | GGTTCCACTCACACG[C/T]GGGCACAGAGCAGGA | 138151 |
| rs527534312 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136073979 | CAGGGATTTGCACAG[A/G]CTCCGTCATGTCCTT | 138151 |
| rs527546178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014705 | AACGATGAGGGAGAC[A/G]GAATCCCCTGGCTGG | 138151 |
| rs527547967 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136068740 | TTCAAAAATAAAAAC[A/C]CAGATAAACCAAAAG | 138151 |
| rs527566991 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136097282 | GGCGCGATCTCAGCT[C/T]ACTGTAACCTCTGCC | 138151 |
| rs527568054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136091649 | CCCTATACAAGGGTG[C/T]GTGCTTCCAAAACCC | 138151 |
| rs527592089 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014226 | AGCCACAGCGCCCCC[C/G]ACCCTCCCCAACGAG | 138151 |
| rs527607083 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136092863 | ACCGGCCACAGTCCA[A/G]CTGGATCTCGGAACC | 138151 |
| rs527633872 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096698 | GTGGGAAGGAGGTGG[A/G]GTAGGAGGGTTCTGA | 138151 |
| rs527649683 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136023679 | CTACATCCATCCACA[A/C]GTTTCTCAGACTTGC | 138151 |
| rs527680399 | in-del | -/AAAA | 0.499933 | 0.00579035 | intron-variant | NACC2 | GRCh38.p7 | 9:136071543 | GTGAGACTCCATCTC[-/AAAA]AAAAAAAAAAAAAAA | 138151 |
| rs527680886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136058803 | CCCACCTGCACACTT[C/T]GGGCAATGCCTCACG | 138151 |
| rs527683123 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136064254 | TGACTGCACTACTGC[A/T]CTCCAGCCTGGGTGA | 138151 |
| rs527763610 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136022175 | TGAACTTGGTGGCAT[A/C]AGGCGCAGAGCAGGT | 138151 |
| rs527782614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136083072 | ACCGAGCACTTCACA[C/T]GGCAGAACCTTTCTG | 138151 |
| rs527837336 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136031398 | GCTGGGGTGCAGTGG[C/T]ACAATCTCGGCTCAC | 138151 |
| rs527838586 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136025222 | AGAATGTGGGCACGG[G/T]CGCTGCTGGATGGCA | 138151 |
| rs527893118 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136030748 | CTCACTACAACCTGC[A/G]CCTCCCAGGTTCAAG | 138151 |
| rs527899954 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136047158 | CCTGCACGGCCTGGC[A/G]AGGGCAGCAGCCAGC | 138151 |
| rs527907052 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136078663 | CATCGGGACAGAAAG[C/G]GGCGTGGGAATGGCT | 138151 |
| rs527922055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136083396 | AGAGGGAGTGGGGCA[A/G]GTGGACACTTTGGCC | 138151 |
| rs527932879 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NACC2 | GRCh38.p7 | 9:136075105 | ATTCCACCTTGTCCT[C/T]AATGGCGGCTTCTGC | 138151 |
| rs528000117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136079103 | TAGTTTAGGGCACGT[A/G]ACCTGAAATCTACTC | 138151 |
| rs528030369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136025663 | TCATGCCTGTAATCC[C/T]GGCACTCTGGGAGGC | 138151 |
| rs528039997 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136065001 | GACGACTGGATAGCC[A/G]CATGCAAAAGAATGA | 138151 |
| rs528062909 | in-del | -/AAATT | 0.0031936 | 0.0398322 | intron-variant | NACC2 | GRCh38.p7 | 9:136055646 | GAAGGGAGGCGAGAA[-/AAATT]AAATTAAATTAAATT | 138151 |
| rs528072301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012261 | TGGCCTGGTCAGGCC[C/T]AGCAGCCTTGGCCGT | 138151 |
| rs528072579 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007345 | GTGACGTGCACGCGC[A/G]TGCACACACACAGAC | 138151 |
| rs528162472 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136056342 | GGCCAGGAACTCCCC[C/G]CAACCCCGAGGCCCC | 138151 |
| rs528169697 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136084790 | CACTCCCTGCAACCC[A/G]GAGGAGCCGTGGGGA | 138151 |
| rs528170029 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136090031 | AAAAGTATCAATATA[C/T]AAAATTTAACAAAGG | 138151 |
| rs528237706 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008037 | ATGTTCTAGGAGCCC[C/T]GACCCGCAGTCACCA | 138151 |
| rs528239035 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007666 | AGCTGAGGACAGCTA[C/T]GAGCTCTGGATTCTG | 138151 |
| rs528274587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136034818 | ATAATTGGGGGCCAG[A/G]CACAGTGGCTCATGC | 138151 |
| rs528303782 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136080670 | GGAAGGACACTCCAC[A/G]GAGCTCTTGCTTATC | 138151 |
| rs528343225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136076824 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCTTCT | 138151 |
| rs528352433 | snp | A/G/T | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136028887 | GCCAGGTGTATGTGC[A/G/T]CTCAGGGCAGTGCTG | 138151 |
| rs528415049 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NACC2 | GRCh38.p7 | 9:136067296 | AAAAAATTGTTGTTG[C/T]CTAGAGCCGGGAGCA | 138151 |
| rs528425777 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136026746 | CCTAACCTACAAGAA[C/T]AGTATACAAACTTTT | 138151 |
| rs528430789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136028664 | CCAAGTTGGAGGGGT[A/G]GGAGTTCCACCCTCC | 138151 |
| rs528454710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136023512 | CAGGCCTGGCAGGTG[C/T]TGTCATTTTATCTCC | 138151 |
| rs528473043 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067291 | AAAAAAAAAAATTGT[A/T]GTTGCCTAGAGCCGG | 138151 |
| rs528476574 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136017616 | GAAGATCAGCTCCCC[A/T]GAGCGGGCCCCCGGT | 138151 |
| rs528519656 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136077049 | GCCGGGTGTGGTGGC[A/G]GGCGCCTGTAGTCCC | 138151 |
| rs528530739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136071934 | CCACCCAAGCCTCAC[A/G]CCCCATTCAAAATTA | 138151 |
| rs528562972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067500 | GTTCTCTGAACACCG[C/T]AGGTGATTTTGTCGT | 138151 |
| rs528580702 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136017896 | AGCCTCCACCTGCCC[A/G]ATTGCACGAGGGCAG | 138151 |
| rs528589419 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012869 | GAGGCAGAAGCCGGC[C/T]GAACAGATGGCAAAG | 138151 |
| rs528630640 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136095648 | ACCTGGAGCGCCGCC[C/T]TCCGCCCTCCCCGGG | 138151 |
| rs528638668 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008379 | CACCACCTGCCAGGC[A/G]GCAGCTCCAACACGG | 138151 |
| rs528731711 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136057248 | ATGGCCCCTGGCCAC[C/G]AACACGCTCATCTCT | 138151 |
| rs528790971 | snp | C/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011477 | AACGCATGCAAGCAG[C/G]TCTAGTACTCGGTCC | 138151 |
| rs528809606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136037857 | GAGTAGGTTATATGG[C/T]TAAAAAAAAAATGAA | 138151 |
| rs528950868 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015307 | CCACCCAGCCGCCCC[A/G]GCAGCCCAGCACTGC | 138151 |
| rs528955565 | in-del | -/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136053611 | GACACAACCCGGGCA[-/G]GGGGGGTACAAGAGA | 138151 |
| rs528955593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136069565 | AAACAAAACAAAACA[A/G]AACAAAACAAAACAA | 138151 |
| rs528988661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136020243 | TCTGGAGGGAAACCG[A/G]GTCTCATTGGCCTCA | 138151 |
| rs529049094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136092688 | AAGGTGGACTGGGCC[A/G]GAGGAGCAGCAGAGT | 138151 |
| rs529081151 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136065629 | GGTTTCAGATACATA[A/C]ATAAGTAAATAAACA | 138151 |
| rs529095791 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136084436 | TGGGGCAACGTCCAA[C/G]AAGGCGGTATCTCTG | 138151 |
| rs529106114 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006410 | CTGGCCTGGGGACGC[C/T]GCTAACAGGGACGGG | 138151 |
| rs529191649 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011171 | CGGGCAGGAGGAGCA[C/G]GAAGGGCAGGGAGGA | 138151 |
| rs529197967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136093022 | CACTGACGGTGGCTG[A/G]GGCCACTGGGCACTC | 138151 |
| rs529248516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136031935 | ACAGCTGATGTGTAT[A/G]GGCAGCTGTTAACAG | 138151 |
| rs529300098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136052455 | GGGGAGGGGGTGAGG[A/G]GGTCAGGACAGCTAG | 138151 |
| rs529338253 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136083748 | AAGAAGAAATTCCTG[C/G]TGTTTCAGGCCTCCC | 138151 |
| rs529351320 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136028429 | TCACCCATGCTGGAG[G/T]GCAGTGGTGCGATCT | 138151 |
| rs529379947 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136032206 | CATCCAGAGGCATGT[A/G]TAACAGAAGGCTGCC | 138151 |
| rs529382257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136026522 | AGGGGTCCCCAGACC[A/G]ACCAAGGACATGGAG | 138151 |
| rs529399634 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | NACC2 | GRCh38.p7 | 9:136080098 | CAGTCCCTACCCCGG[G/T]CGTGGCTGCCAGCCA | 138151 |
| rs529412272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136084386 | GACTCATCCATCACA[C/T]AGACACCTCCTACGC | 138151 |
| rs529466198 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136027005 | AGGCTGAAGCAGGGG[C/G]ATCACCCAAGGTCAG | 138151 |
| rs529486294 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NACC2 | GRCh38.p7 | 9:136021065 | GAATGAAAAACTTCC[A/G]ATCTCTGAATGAAGA | 138151 |
| rs529527853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136016877 | CCAGCAGGGCAGCCA[C/T]TTCTGGGGCCACAAA | 138151 |
| rs529542312 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136093373 | GCCCAGGGCAGAGCA[A/G]CCCTGCGAACCCTTC | 138151 |
| rs529636874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136037610 | CCTCCTAGGTTCAAG[C/T]GATTCTCCTGTCTCA | 138151 |
| rs529664723 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | NACC2 | GRCh38.p7 | 9:136057512 | TAGAAGGTTTCCAAA[A/G]AATTAAGCTGTGTTT | 138151 |
| rs529680444 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | NACC2 | GRCh38.p7 | 9:136085932 | ATGGGAGGGGCTGGC[A/G]GAGCCCGGAGGCTGG | 138151 |
| rs529771354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136029240 | AACCCCAGACTCAGC[C/T]AGACAACAGGATGGC | 138151 |
| rs529795136 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031138 | TTGCCTATGACATTT[C/T]TTCAAAGGTTTAAGA | 138151 |
| rs529805488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136081980 | AGGGTGGAGCTGACG[C/T]GAGAGCCAGGCTGCA | 138151 |
| rs529807664 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136024003 | ATGGAGGAAGCTCCC[A/G]GGATGTGTGCCAGCT | 138151 |
| rs529823296 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136060256 | CTCTTTTGCAACACC[A/G]AAGAATCTTGTGTAA | 138151 |
| rs529858800 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136029825 | GGCCTGGAGCTTGCT[C/T]GCTCACACACCCCTT | 138151 |
| rs529862131 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136062636 | AAAAATTATACAGGC[C/T]GGGCACAGTGGCTCA | 138151 |
| rs529920149 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136023616 | GGCCTCCGACAGGGA[A/T]CCCAGCGATGATTTT | 138151 |
| rs529959478 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136073883 | TGGAGTATCTGGTCT[A/G]CCCAGAAGCAGGGTC | 138151 |
| rs529970156 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136018926 | ACCACCTCGTCTCGA[A/G]ATGTTTTTCTAAACA | 138151 |
| rs529984831 | snp | A/C | 0.0221141 | 0.102801 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136095822 | CCGCCCTGGACGCTC[A/C]GGCGGGCCGTGAAAG | 138151 |
| rs530024334 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136063627 | GGTGGCTCACGCCTG[C/T]AATCCCAGCACTTGG | 138151 |
| rs530095657 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009292 | TCCAGGTTCCCAGCG[A/G]GCCCCATGGGGGCTC | 138151 |
| rs530097458 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014203 | GGAACTAAGCAGGGG[G/T]TGGGGAAAGCCACAG | 138151 |
| rs530114717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136086922 | CACACCACACCGGGG[A/G]TTCGCATCTACCTGA | 138151 |
| rs530176342 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136091588 | GACAAGCAACCAATA[A/C]TTCCAGACAGATGCC | 138151 |
| rs530200625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136087391 | CTTCCCTCCTCCTGG[C/T]CTGTCACCTGCACAG | 138151 |
| rs530200688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136082633 | GGAGACCCTCCACCC[A/G]CCAGGCCCGCGCTGC | 138151 |
| rs530263946 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009761 | TCCCCTAGCGGAGGC[A/G]GCCTCCGCTTGATGG | 138151 |
| rs530309210 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136045486 | AGTGACATCTGCCAG[C/G]TGCAATTAAACATCT | 138151 |
| rs530322401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136078561 | ACTGGCCCTGGAACC[A/G]TACCTGGATGCATAG | 138151 |
| rs530325054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136043361 | TGAAACGTGCTCAGC[A/G]TTACTGACCATCAGG | 138151 |
| rs530381195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136093112 | AAGGTGGAACCTTGG[A/G]AACTCAACATCCCGA | 138151 |
| rs530411338 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136060906 | CCCCCAACACAGCCA[A/G]TCCCTGAGAGACTGG | 138151 |
| rs530452023 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136030605 | ACAGAGCAAGACTCC[A/G]TCTCAAAAAAAAAAT | 138151 |
| rs530471169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136065764 | GAAGGGGCTGGAGCC[A/G]TGATCACGCCACTGT | 138151 |
| rs530489757 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136068539 | TGTGCAATGACATTA[C/T]GATGGCTACATCGTC | 138151 |
| rs530495431 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136029165 | TTGCCTTTTCCGGGC[C/G]CACTCATGGCTGCCC | 138151 |
| rs530500602 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011329 | CTGCCAGTGGCCTAA[C/T]TGTTTACAGTATAAT | 138151 |
| rs530502570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016169 | TTTTTTTTTGACTGA[C/T]TGGTGATGAGTACAT | 138151 |
| rs530503064 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136088876 | CAGCCCAGCCCCCGG[C/G]ATCCTGGGGGAAGGT | 138151 |
| rs530510555 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136066265 | AACCATACAAGAGAC[G/T]TATATCTAGAATGTA | 138151 |
| rs530565452 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136006538 | CAAGTCCAGGAAACT[C/T]AGGTTTGAACTGACT | 138151 |
| rs530583638 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007286 | ACACGAAAAACCTTT[C/G]CCATTTTAGAACCAT | 138151 |
| rs530600580 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136061384 | TCAGATAGAGGGGTC[A/C]CCTCCCTCCAGGCCC | 138151 |
| rs530670194 | snp | C/T | 0.000429507 | 0.0146482 | missense | NACC2 | GRCh38.p7 | 9:136011776 | CGATGGTGGCGGCGT[C/T]GCCCCGCCGCTCGGC | 138151 |
| rs530672155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136093346 | TTTTTTAAAAGTCAC[C/T]ACTAGCCCCCTGCCC | 138151 |
| rs530708780 | snp | G/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009804 | GGGGGAGTGGGGTGC[G/T]CTGGTCGGCCACCGC | 138151 |
| rs530719248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136084753 | CATACATCACGCAGC[C/T]TGGAGAAGGGACGGG | 138151 |
| rs530721919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136056326 | GGCCAGGGCCCTCGG[C/T]GGCCAGGAACTCCCC | 138151 |
| rs530734331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136055849 | CAGTTAGTTAAGTGA[A/G]GACATCTCCTAAAAG | 138151 |
| rs530746532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136027174 | AGGTTGCAGTGAGCC[A/G]AGATAGCGCCACTGC | 138151 |
| rs530767834 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136028586 | AGTGGGTGAGGCGTG[C/G]CCAGGGCTGCACGCT | 138151 |
| rs530845699 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008238 | CCAGGCGCGGCCCGC[C/T]GGGCTCACAGTATCT | 138151 |
| rs530859158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136032690 | TCACTTGAGATCAGG[A/G]GTTCGAGACCAGCCC | 138151 |
| rs530874193 | snp | C/T | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012851 | CCACACGCCCAAGAG[C/T]GGGAGGCAGAAGCCG | 138151 |
| rs530919152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136017119 | CAGGCTGGCCGACAC[A/G]CCACCGCCACCGCCA | 138151 |
| rs530931037 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136076781 | TGGGAGGCTGAGGTG[G/T]GTGGATCATGAGGTC | 138151 |
| rs530932411 | snp | C/G/T | 0.00637319 | 0.05614 | intron-variant | NACC2 | GRCh38.p7 | 9:136058112 | ACTGGGGGCGGGGGG[C/G/T]GCCCAATGACGCCTG | 138151 |
| rs530954217 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136027931 | TAATGGAAACTCTCT[A/C]GCAAGTCTGAACAAA | 138151 |
| rs530969763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136076448 | CCACCAGGCACACAC[A/G]GACAACGCCACGGGG | 138151 |
| rs531071315 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008336 | GGAAGAGGAAGGCAG[A/G]GCAGGAGAGGCGGCT | 138151 |
| rs531085736 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136062762 | TCTACAAAAAAATAC[A/G]AAGACTTAGCCAAGT | 138151 |
| rs531088696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136094159 | AGGAACGCGCAGCAG[A/G]GAACACAGCTCAGGG | 138151 |
| rs531151177 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136094701 | CGAGGCGCGGGCCCG[A/G]CTGGGCCAGGCAGCT | 138151 |
| rs531163018 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136024731 | TTCCCACTGTGGATA[G/T]GAGGGAGCAGCCAAT | 138151 |
| rs531179066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067189 | AACCCGGGAGGCGGA[C/T]GTTGCGGTGAGCCAA | 138151 |
| rs531209874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136090556 | AGTCTTCCCTCAGCA[A/G]GCACCCAGCTCCCAA | 138151 |
| rs531211903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136085425 | TCCAGAGGCTGAGGC[A/G]GGGAGATCACCTGAG | 138151 |
| rs531224189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136030235 | CCTTAGTTTGCAGGC[C/T]GTACAAAAACAGGAC | 138151 |
| rs531244760 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136078008 | CAAACTCCTGACCTC[C/G]TGATCCACCCGCCTC | 138151 |
| rs531276116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014306 | CCCTCCCCAAGAACA[C/T]ACTTTGTTGTTGTTT | 138151 |
| rs531277886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136019519 | ACTCAGGTGCCAGGA[C/T]GGTGCCCTCCAAACC | 138151 |
| rs531284424 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007951 | ACCTTCCGCCTTCCT[C/T]CTGGCTCTAAACACA | 138151 |
| rs531313949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014318 | ACACACTTTGTTGTT[A/G]TTTAGAGACGGGGTC | 138151 |
| rs531396446 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136074663 | ATCTCTGGTTCAACA[C/T]TGACTCAATACTGAC | 138151 |
| rs531429832 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136016682 | TTGTGAACGAGTGAG[C/T]AGAAGATGTGAGGCG | 138151 |
| rs531472520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136059471 | AGCCCAAGGGGAGTG[A/G]CCTGAACTCTGGCTG | 138151 |
| rs531490064 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136092248 | ACTTCGGGGAAGGCC[A/C]AGGACCCAGGGAGCT | 138151 |
| rs531590054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136047831 | CGATGTGAGGGCTTA[A/G]GGCTGACCCAGCACC | 138151 |
| rs531594987 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010840 | ACGGATCGGGCAGAA[C/T]AAGGACAGGGTGTGG | 138151 |
| rs531599019 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136064966 | GGGGAAAGAACAGTC[G/T]TTTCAAAATGTGGTG | 138151 |
| rs531605131 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | NACC2 | GRCh38.p7 | 9:136059765 | GGGGACTGTTGGGCC[-/T]TGTGTGTGTATCCGT | 138151 |
| rs531611599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136092683 | AGGTGAAGGTGGACT[A/G]GGCCGGAGGAGCAGC | 138151 |
| rs531709358 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136019728 | CTGGACCACACGGGG[C/T]GAAGCAAACACAAGG | 138151 |
| rs531713847 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136083457 | CAAAATCCACATGCA[A/C]CCCAAACTCGAATGT | 138151 |
| rs531722348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136031463 | GTGCTTCAGCCTCCC[A/G]AGCAGCTGGGATTAC | 138151 |
| rs531735234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136060055 | GGATGCAGAGATGCC[A/G]GCTGCCCGCATCTGC | 138151 |
| rs531740152 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136091066 | TTAGAGAGACCCGGA[C/G]CCAGCCTCTCCTCCC | 138151 |
| rs531795174 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136070137 | ACTAGAAATCGTAAC[-/A]AAAGGTAACAGGGAA | 138151 |
| rs531803709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136031890 | CCCACCTCCTCTAAC[C/T]GTGAGGTTTTGGCAT | 138151 |
| rs531823486 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NACC2 | GRCh38.p7 | 9:136075181 | TGCAGCAGGCTGCAA[C/T]GCCCCCCACACACAG | 138151 |
| rs531844727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136070202 | CCATATGTCAAAGAA[A/G]AAGTCTCAAGAAAAT | 138151 |
| rs531877820 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136076288 | CAACAATCTATCCAG[A/C]CTCCTCTCCTCAGTG | 138151 |
| rs531891006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136021469 | CCCCCAAGTGCTGGC[A/G]AGGACACGGGGCAGC | 138151 |
| rs531949797 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024932 | CAGGATCCTGAGAGC[C/T]GGCCTCAGGGTGCAA | 138151 |
| rs531959959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136079588 | TCACTGAGTGGAAAG[A/G]CCACTTGGCCCTCAA | 138151 |
| rs531973634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136057054 | TCCAGCAGCCAGTAC[C/T]TCGAGGGAGGGCTGG | 138151 |
| rs531985783 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136056376 | AAAAGCCAGGATGGC[A/G]TGTGCCGTGTGCTCA | 138151 |
| rs532034182 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007926 | AGAGGGGGACCAGCC[C/T]TCCCTCCCTACCTTC | 138151 |
| rs532097998 | snp | C/G | | | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014117 | GGGGAGGAGCAATTT[C/G]AGGTCCCACCTGCTG | 138151 |
| rs532110311 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136090095 | AGCAAAACTCTGTTA[A/G]AGCTGATTTTTTAAC | 138151 |
| rs532118919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136033371 | ACTTCTGGCCGGGCA[C/T]GGTGGCTCACGCCTG | 138151 |
| rs532159934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136029126 | CCAGGCTGTCAGTTC[C/T]GCAGACTGGAGTGAG | 138151 |
| rs532211112 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136042755 | AGACACAGAGACAGA[C/G]ACACACACACAGAGA | 138151 |
| rs532225075 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136072409 | AATTAGCCGGGCGTG[C/G]TGGTGTACACCTATA | 138151 |
| rs532275620 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136063654 | TTGGGAGGCCAAGGC[A/G]GGTGGATCACCTGAG | 138151 |
| rs532287989 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136077052 | GGGTGTGGTGGCGGG[C/T]GCCTGTAGTCCCAGC | 138151 |
| rs532323858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136094794 | TTCCCCACCCGGAGG[A/G]CTGGATCGGCCAGTC | 138151 |
| rs532352718 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136028756 | GCCTGGGAAGCCCCC[A/C]TGCCTGCACAGGCTC | 138151 |
| rs532380293 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136067766 | CTTGAACCCGGGAGG[C/T]GGAGGTTGCGGTGAG | 138151 |
| rs532420100 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136017942 | GGCCCTTGGGCCACC[C/T]GGGGCTGGACCTTGC | 138151 |
| rs532515224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136062866 | AGGCCGCAGTGTGCC[A/G]TGATCGTGCCACTGT | 138151 |
| rs532533577 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136091567 | CCGGAGTTCATGTCC[C/T]CAAATGACAAGCAAC | 138151 |
| rs532536612 | snp | A/C | 0.00993419 | 0.0697739 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136095722 | GCCCCCCTACCCCGC[A/C]CCCGGCGCGCGCCCT | 138151 |
| rs532544912 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013732 | TCCTGGGGCCGACCG[C/G]CCACGGCTGAAGTCA | 138151 |
| rs532578037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067551 | CACTTAAACGATGCT[C/T]GATGGGCCGGGCGCG | 138151 |
| rs532636680 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136075189 | GCTGCAACGCCCCCC[A/C]CACACAGACTTGGCC | 138151 |
| rs532667725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136086884 | CCAGTGCCCTCTACG[C/T]ACTAAAGGCTTTCTG | 138151 |
| rs532683395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136082556 | ACTGGGTCTGGCCCT[C/T]GGAGCCCGACAAACA | 138151 |
| rs532688298 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008498 | AGGCTTAGGGATAAA[C/G]GTGCAGACATCTCAT | 138151 |
| rs532700630 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136089887 | CACAGGCAAGATTAA[C/T]GCCTAAAGGGTTTCA | 138151 |
| rs532742268 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007821 | AGCCCAGGCAGTACA[C/T]GGCTGGGTGGGGTGG | 138151 |
| rs532743646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136042443 | TAGGCCTGCAGGTAC[A/G]TATTCGACTGATTCT | 138151 |
| rs532758632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136057904 | GAGCGTGCTGGGCCC[C/T]GCTGCTGGTCACCCA | 138151 |
| rs532767546 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136065243 | GTAATCCAACACTTT[A/G]GGAGGCTGAGGCAGG | 138151 |
| rs532777699 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015330 | AGCACTGCGCTCGCC[A/T]TCCAGAAGCAGTGCC | 138151 |
| rs532804545 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136075475 | GTCGGCAGCGGCTCC[G/T]TGTGAACCTGCCGTC | 138151 |
| rs532838934 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136019533 | ACGGTGCCCTCCAAA[C/T]CTCTCAGCATGGTGA | 138151 |
| rs532848692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136093050 | CTCGGTGCCCTGTGC[A/G]TTCCAGGGACACAGG | 138151 |
| rs532867941 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136029886 | TGTGGGATCCGGGCC[A/G]GTAGTGCAAACCTGG | 138151 |
| rs532932617 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010955 | GCACACACACACACT[C/T]GTGCACACACCCCAC | 138151 |
| rs532935101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136093304 | AGCCTCATGCTTTAA[C/T]TGGAAAACAAAGGGA | 138151 |
| rs532935237 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136063140 | CAGGTCTGTCGATCT[C/G]TCTCTCTCCTGTCAA | 138151 |
| rs532939249 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006438 | GGGGTCCTGAGGGTG[C/T]CCCTGGGGGACCATT | 138151 |
| rs533009708 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011217 | CACCAGGGGCCTGGC[A/G]GCCTCCCACCCTCCC | 138151 |
| rs533043073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136078976 | TGATGCCGCGCCGCC[A/G]CCGCCCCTCTCCGAT | 138151 |
| rs533047703 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015727 | GAAGATGCCCATGGC[A/G]TGGGTCAGACTGGCT | 138151 |
| rs533087059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136083805 | CGTTCCGGCCGCCCA[C/T]GACATTCATCTCGAC | 138151 |
| rs533097588 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007182 | TGGAAGCGACTGATC[A/G]GAATACGAGCCGGTC | 138151 |
| rs533102514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136031958 | GTTAACAGCTTTCCC[A/G]ATGCTAGGGCCTGGT | 138151 |
| rs533148432 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136055203 | GGAGCCCGCGGGGAG[A/G]ACAGGGGCTCACTGG | 138151 |
| rs533228863 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136022044 | GGGGGCAGCCTGCAC[A/G]ACTCTAGGTGGCCTC | 138151 |
| rs533267291 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136088840 | CCCACAAAGGGACCT[A/C]CCCCAAGCCCCGAGG | 138151 |
| rs533290551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136021582 | AACATACACTTATGA[C/T]CCAGCAATTATACTT | 138151 |
| rs533291424 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136055801 | GGAGAGTCCCTCTAC[C/T]CCGAGCCCCGGCCCC | 138151 |
| rs533292055 | in-del | -/AC | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136042756 | GACACAGAGACAGAG[-/AC]ACACACACAGAGACA | 138151 |
| rs533298190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136085609 | GAGGGGCCTGGGAGG[C/T]GGCTGCCAGGGGGTG | 138151 |
| rs533311280 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136027149 | AGAATTGCTAGAACC[C/G/T]GGGAGGCGGAGGTTG | 138151 |
| rs533410752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136061894 | GGAGGCCAAGGCGGG[C/T]GGATCACCTGAGGTC | 138151 |
| rs533417430 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136076355 | CAGGTTTCCTGCCCA[A/T]ACCACGACAAAAATG | 138151 |
| rs533420269 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012719 | TTCTTGGGCCGAGGG[A/C]CACAGGAGGCTGTGC | 138151 |
| rs533426786 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136020665 | AACTTAAATGCAAAT[A/G]GACAGAACAGTGCTG | 138151 |
| rs533433801 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136081407 | AGCCATGGTTCCCAT[C/T]CTCCACGCGTCCTCC | 138151 |
| rs533493766 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | NACC2 | GRCh38.p7 | 9:136059595 | TCCCTCCTCCAGCAA[C/T]GCGTCCAGGTCAGCA | 138151 |
| rs533543610 | snp | C/G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074255 | GGAGATCCAGACCAT[C/G/T]CTGGCTAACACGGTG | 138151 |
| rs533600682 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136090832 | GCTGAGCTGGGGCCG[C/G]CCAGCCCTGGGCTTG | 138151 |
| rs533603127 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136067608 | TTTGGGAAGCCAAGG[C/T]GGGCAGATCACGAGG | 138151 |
| rs533613994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136071349 | GGAGTTTGAGACCAG[C/T]CTGGCCAACATGGTG | 138151 |
| rs533645730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136089444 | TCAGAGAACTCAAGG[C/T]CCTTCAGGTTCTGCT | 138151 |
| rs533645843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136094116 | TGCCTTGGGCACCCC[C/T]GGGTCAGCACCCCCG | 138151 |
| rs533663162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136018014 | GATGGGAAGTCCCCC[A/G]GTGGGGGGCGGGGGG | 138151 |
| rs533663494 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136090101 | CTCTGTTAAAGCTGA[-/T]TTTTTTAACAGCACA | 138151 |
| rs533665345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136072563 | AAAGAAAAGAAAAGA[A/G]AAAAAAGGCTGGGTG | 138151 |
| rs533701378 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136059626 | GGCCCAGCAAGGAAC[C/G]TGAGCAGGCCGCAGG | 138151 |
| rs533758517 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | NACC2 | GRCh38.p7 | 9:136074950 | TCCTTCTGGGAGCCC[-/G]GGAGCTCTGTCCCCC | 138151 |
| rs533782111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136017729 | TGAGGGCGGAGCACC[A/G]CCTCCCTCATTCCTG | 138151 |
| rs533799382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136058137 | CGCCTGGAGCCACAC[A/G]CCTCTAGGCCCTGGC | 138151 |
| rs533890533 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136091249 | GAAGGCAGAAAGGCC[A/G]GGCTGCCCACATTCA | 138151 |
| rs533906191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136082250 | GGTGTGGCCACGCCA[C/T]GGCCTGATGGAAGGG | 138151 |
| rs533941260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136042679 | ACACACAGACACACA[A/G]ACATACACACACAGA | 138151 |
| rs533948588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136090924 | GGCCCCTCTGTTCCC[C/T]GCCCCCAGCCCTGCC | 138151 |
| rs533964498 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008778 | TCCGCTCAGCAGCCA[C/T]GCACGTCCACAGACA | 138151 |
| rs533999165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136095093 | GCGCCAAGTTGGGCG[A/G]CCGCGGAGTTTGCGG | 138151 |
| rs534029184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136077887 | GGTGTGCCTTTGGGA[A/G]TGAAAACCACGTAAA | 138151 |
| rs534120629 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136075574 | AGGACGCATCTTCTT[G/T]TATCGGGCATAGGCC | 138151 |
| rs534156895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136074147 | TCTCCACAAATAATT[C/T]GTTAAAAAATTAGCC | 138151 |
| rs534173093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136086994 | ATATCATTAGTGAAA[A/G]GTAAGATGAGATATC | 138151 |
| rs534186203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136043616 | CGCTGCACGGTCTCA[C/T]GCACAGGGATCCTAT | 138151 |
| rs534237508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014431 | CACCTCAGCCCCCTG[A/G]GTAGCCGGGACCACA | 138151 |
| rs534248724 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136097134 | ACTGAATTCCAGGCC[C/T]GTGCTACTGAGTATG | 138151 |
| rs534263218 | in-del | -/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007903 | GGTCAGGCACTAGAG[-/C]CCCCCTCAGAGGGGG | 138151 |
| rs534292469 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136084015 | AAGACCTGGCCACAA[C/T]CCCATCTCCTAGTTC | 138151 |
| rs534292771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136088963 | CTCTGATAATGATCT[C/T]GGCATCGCGTGGAGC | 138151 |
| rs534314934 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | NACC2 | GRCh38.p7 | 9:136024223 | GTGTGTGTGTGTGAG[A/G]ACAGAGGGTGTGTGT | 138151 |
| rs534328727 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136020119 | CTTAGCATCACCGAA[C/T]CACGCACGTAAAAGT | 138151 |
| rs534329610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136030331 | GAGGGTACTGGAGGC[C/T]GGGCGCGGTGGCTCA | 138151 |
| rs534393136 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136032375 | GTTACAATGCAACAC[C/T]TACGAGGAAAAAAAA | 138151 |
| rs534406063 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136063433 | ACACCTCCCTCTGAG[A/G]TAAGAAGAGGGGCCA | 138151 |
| rs534407937 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136024821 | CCTGAGGGGCTGCGA[G/T]CCTGAGAACTGGGAC | 138151 |
| rs534408930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136080327 | CATGGGATGCCACCT[C/T]TCAGGGCATCCAAAA | 138151 |
| rs534418971 | snp | A/C | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136095853 | ACGAGGATACGGGAG[A/C]GCCCTTGGGCGAACG | 138151 |
| rs534422413 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136079879 | GGGCCAGGCCACAGC[C/T]GTGCTGTGGAAGGAG | 138151 |
| rs534478953 | snp | A/G | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096892 | GGGCAGGCCTCAAGG[A/G]GCTACCCACTAGGAC | 138151 |
| rs534481062 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015025 | CTGCTTCCAGGAGCC[C/T]GTGAGTGCCCATGAC | 138151 |
| rs534522950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136074835 | TCACTCAGCCTCGGC[A/G]TCTACACCTCACACA | 138151 |
| rs534583725 | snp | A/G | | | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006206 | TAAAACCAAGGTCCC[A/G]AAAAGGAGACCCCCC | 138151 |
| rs534614272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136055503 | AGCTCCATGGTCTGA[A/G]GGCCTCGCCCAGAGT | 138151 |
| rs534628993 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136076517 | GACAGGAAGCAGAAC[A/G]GAGGTTTCCAGGGGC | 138151 |
| rs534660558 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136083007 | GTCATAACTTCTGCC[C/T]CATTAGACATCTACA | 138151 |
| rs534696613 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012341 | AGCCCCAACGGCTAA[A/C]GGGAACTGGTCAGAG | 138151 |
| rs534723390 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012034 | AGTACACTGTGAGGA[A/C]GGGGCGGCGTGAGCT | 138151 |
| rs534763881 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136062270 | CCCCCCAACGCCAAG[G/T]GACCACCCAGCAGTC | 138151 |
| rs534796019 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007772 | TTTTCCACTTGCTGC[A/C]AAGATGTTTCCATAA | 138151 |
| rs534822703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136027182 | GTGAGCCGAGATAGC[A/G]CCACTGCCCTCCAGC | 138151 |
| rs534846772 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136076133 | AACTCAGTAGTGATG[A/C]CACCCCATACCCCGT | 138151 |
| rs534871378 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136066535 | AAGAGATGTAGCGAT[C/T]GGGAATGCAAAATGT | 138151 |
| rs534878897 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136085556 | CAACAAGTAACTGTA[C/G]TGAGGGGTCTGCACT | 138151 |
| rs534896715 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136035441 | CATTCTACAAAATAA[C/T]GAACTGCGCTTTTCA | 138151 |
| rs534908413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136057148 | GGCGTTGGCTCTGCC[A/G]GGGGTCTGGTCCAGG | 138151 |
| rs534916977 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078530 | CTGAGGCTTGGAGGT[A/G]GGACGTGGCCCGCTC | 138151 |
| rs534930483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136016610 | ACTGGCTTCAGCCTG[C/T]CCCATCCCTACTTGG | 138151 |
| rs534978812 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NACC2 | GRCh38.p7 | 9:136065931 | GGGCATGGTGGCTCA[C/T]GCTTGTAATCCTAAC | 138151 |
| rs534996096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136062024 | ACTCAGGAGGCTGAG[A/G]CAGGAGAATCGCTTG | 138151 |
| rs535054632 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136067776 | GGAGGCGGAGGTTGC[A/G]GTGAGCCGAGATCGC | 138151 |
| rs535075517 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014384 | ATCATGGCTCACTGT[A/G]GCCTCGACCTCCCGG | 138151 |
| rs535086698 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136062586 | TACATAATACCTGTT[A/C]TCTGTACGTTCACAC | 138151 |
| rs535098765 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136060377 | GGGGCCATAAAAGGT[A/G]ATTACCGATATGAAA | 138151 |
| rs535102420 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136084952 | GGAGTTTGTGTCTAA[A/T]GGGGAAAGGGGTTCA | 138151 |
| rs535108273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014043 | GGCGCACAGATGGGT[A/G]AGGGGGAGGGGGGGA | 138151 |
| rs535146647 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010460 | CCACCCGGGACCCCC[C/T]TTTTCCCCCAGTGGG | 138151 |
| rs535162239 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136059065 | GGGCAGGGGAGAAGC[C/G]TGATCTGGAACCCAC | 138151 |
| rs535191603 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031921 | CTGCACCAACACCCA[C/T]AGCTGATGTGTATGG | 138151 |
| rs535242221 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136091706 | GCCACAGCTGAGGGA[C/G]CTAGGGCTCCCAGCA | 138151 |
| rs535337936 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136045065 | CAGGGTCCAGGATGT[C/G]GGCAGCTGGTCTGAG | 138151 |
| rs535355046 | in-del | -/A | 0.030278 | 0.119257 | intron-variant | NACC2 | GRCh38.p7 | 9:136027632 | ACAAGGGCAAAAGGG[-/A]AAAAAAAAATCACAA | 138151 |
| rs535380459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136078834 | CTCCAGGAACTGAGG[C/T]TCTCAGGGCAGGGCC | 138151 |
| rs535403100 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136022679 | CCTGGCACACAGCAT[A/G]CGCCTAACACACAGG | 138151 |
| rs535435723 | in-del | -/AAAAC | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136025436 | TAGACCAAATGATAA[-/AAAAC]AAAACAAAACAAAAC | 138151 |
| rs535455780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136026045 | CCAGATTGATGCAGA[A/G]TAAGAAAGAATAGGC | 138151 |
| rs535462068 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136019119 | AGCTCGTCCGCAAAG[C/G]TGCCTCAATGTCTTC | 138151 |
| rs535467894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136025302 | GAGGAGTGCTGCTTA[C/T]GACTCCTCACCTGTT | 138151 |
| rs535476765 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136068288 | AGATGACCTGAGGTC[A/T]GGAGTTCAAGACCAG | 138151 |
| rs535481671 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136064904 | CTACAAATGTATTCA[G/T]GTGTCTGCAGCCAAT | 138151 |
| rs535510113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136074891 | AGCCGAGGCGGAGTC[A/G]GCAGGGCCGGGGGAT | 138151 |
| rs535512580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136069835 | ATGAAGCACAAACCA[A/G]TAGAACTAAAGACAA | 138151 |
| rs535515927 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136092142 | CGCTGGCCAAGCTCC[A/C]CCACCCAAGGCCCGA | 138151 |
| rs535526112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136087158 | CAGGACAGTGGCAGC[C/T]TTGGGAGCTGGAGGG | 138151 |
| rs535614631 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136087672 | GCGGGAAAACTGAGA[C/G]CCAGGGAGGCCATGG | 138151 |
| rs535622675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136046606 | GCTGCGGGTGGGGGG[A/G]CTTGAACTCGGCCCC | 138151 |
| rs535632276 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136065826 | CAAAAAAAAAAAAGA[A/G]AAGGAAAGAAAACCC | 138151 |
| rs535634928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136092809 | CCTGGGGTAAGGGGT[A/G]CCACCTGCTGCCCCC | 138151 |
| rs535651625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136060499 | GGGCCAGGCCCAGGC[C/T]CCATCCCTCTCCCCT | 138151 |
| rs535661555 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015850 | GAGGCCCGGCCCCCA[A/C]GGGCTTCTGGACTCG | 138151 |
| rs535685299 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136065499 | GTGGCGCACGCCAGT[A/G]GTCCCAGCTACTCAG | 138151 |
| rs535709797 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136066520 | GTTGGTGGAAATGTA[A/C]AGAGATGTAGCGATC | 138151 |
| rs535712823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136070224 | CAAGAAAATCAAATA[C/T]GGGCCGGGCGTGGTG | 138151 |
| rs535773580 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NACC2 | GRCh38.p7 | 9:136019683 | GGCAGCAGGGCCCAG[C/T]TACTGAGGGTAGGCA | 138151 |
| rs535833280 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136080147 | CCCACAAAAGCCAAC[G/T]GTTTGACCACAAGGG | 138151 |
| rs535840492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136081052 | AGAACCCCACGGGCC[C/T]AGGGTCACGGATCAC | 138151 |
| rs535841362 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136028883 | CCTGGCCAGGTGTAT[C/G]TGCGCTCAGGGCAGT | 138151 |
| rs535884456 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136079244 | CACTCTCTGAGCTGA[G/T]GGGGAGACCAGGGAG | 138151 |
| rs535949239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136071639 | GCAAAGGAATGAAAA[C/T]AGCTAAGACAATTTT | 138151 |
| rs535959338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136020567 | AGGGAGACGGGGAGG[C/T]CTACTCCCTAAAAGT | 138151 |
| rs535997826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136022936 | CTGTTAAGACACAGC[C/T]CGTTTCGTGGATGCT | 138151 |
| rs536031943 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136092214 | TGCCAGGAAAGGAAC[A/G]AAATGCTGGGGAGAG | 138151 |
| rs536047519 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136084415 | GCAATGTCCGGTCTC[C/T]GCTGGTGGGGCAACG | 138151 |
| rs536080421 | in-del | -/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136018265 | TGAGCCTCGGGGCGT[-/G]GGGGGGCTGCCAAGG | 138151 |
| rs536086098 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136017699 | TAGGCTGCCAGCACA[A/G]CCACCCTGCTCAGGT | 138151 |
| rs536119251 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136006628 | TGTTTGTCATGGATT[C/T]CCACTGTCTGAAACG | 138151 |
| rs536141017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136090812 | CTGCCCTCGGGGCCC[C/T]GGTGGCTGAGCTGGG | 138151 |
| rs536157857 | snp | C/T | 5.82033e-05 | 0.00539428 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011487 | AGCAGCTCTAGTACT[C/T]GGTCCCTCGCGCAGC | 138151 |
| rs536194217 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136093203 | AAACCAGGAAAGCAG[A/G]ACTCCGGAGGCAGAG | 138151 |
| rs536198940 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136094956 | GCGCCTCCGCCGGGA[C/G]CCCCCGGCCCCGCCC | 138151 |
| rs536214438 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136086059 | GAGTCCGGGCGCCAC[A/G]CAGGGCAGCTCCGAC | 138151 |
| rs536244924 | in-del | -/AAAC | 0.00199481 | 0.0315187 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007261 | TTTTCCAAAGAAACA[-/AAAC]AAACAAACACGAAAA | 138151 |
| rs536247143 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031255 | CTTGATATCAAAACA[C/T]TGGGAAGGTAAAGAG | 138151 |
| rs536340647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136082130 | CCCTGGGTCAGCTCA[C/T]CACTAAAGCAGGTGA | 138151 |
| rs536354652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136081615 | TGGTGTAATTATTAC[A/G]AAAGCACACTTAAAG | 138151 |
| rs536395954 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136029650 | CTGCAGTTCCTGGCA[C/T]CTCCAAGCTTCCAGG | 138151 |
| rs536395986 | snp | C/T | | | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006502 | TTCTCTGTGTCTCCC[C/T]CAAACCCCACAGGGC | 138151 |
| rs536404714 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136094513 | CCGCTGAGTTTCTTA[C/G]AGAAGGAGCTGGGGC | 138151 |
| rs536439208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136017975 | GCCGAGGGCACGGCA[C/T]GGTCCCCTCGGCAGC | 138151 |
| rs536441541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013076 | CAATCAGACCATGCT[C/T]GGCCCCCAGGGACGG | 138151 |
| rs536476913 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136077833 | TGAAAAGTGAATAAG[A/G]AATCAGTGATGAATA | 138151 |
| rs536517118 | snp | G/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008721 | CGGGCCGCCGCCCCC[G/T]CCCCACGGTACATTC | 138151 |
| rs536555781 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008183 | GGTGGACAGACACAA[C/T]GCGGAAAACAAGACA | 138151 |
| rs536557427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013386 | ATGCCCTGCTGGGAG[A/G]CCACTTGGCCTCACC | 138151 |
| rs536560029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136018719 | TTCCCGGTGGGGCAG[A/G]GCATCGCAGGATAAG | 138151 |
| rs536587073 | snp | A/G | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012804 | CGGGCCGGGGGCGGC[A/G]GTCTGCCCTGGAGAT | 138151 |
| rs536616862 | snp | C/T | | | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006407 | CAGCTGGCCTGGGGA[C/T]GCCGCTAACAGGGAC | 138151 |
| rs536619195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136091184 | GAGCCTTACATGGGA[C/T]TCAGTGGCTTCACTG | 138151 |
| rs536716587 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136029549 | CCACCACGTTGTGGG[A/C]AATGAGGAGAGAAGA | 138151 |
| rs536718390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136042615 | GCAAAACTGTTAAGA[C/T]TTTTGCAAGAAAACA | 138151 |
| rs536727740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136083893 | GATGTCCACCAAGAA[C/T]CTGGCTGGCCCAGGC | 138151 |
| rs536771047 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136086856 | TGTCCTGGGCAAGTG[C/G]AGAGCCAGCCCCCCA | 138151 |
| rs536789931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136083624 | AGGCCGAGACTGGCA[C/T]GAGACGGGCATGAGC | 138151 |
| rs536794540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136088559 | TTGGGGCTCGTGGGG[A/G]CCCAGGTCCGGTGAC | 138151 |
| rs536848047 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136029945 | TGAGCCCAGCAGGCA[A/C]GAGCAAAACTTGGGT | 138151 |
| rs536947781 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136074027 | AATTAAGATCTTGGC[C/T]GGGCACAGTGGCTCA | 138151 |
| rs536986757 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136024769 | TAACTCCCTCATCAA[A/C]AACAACTACCAAAAT | 138151 |
| rs537026684 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136049143 | AGGAACGGAGAGGAG[C/G]GGGAGCGACTGCTCA | 138151 |
| rs537066321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136092774 | AGGCCTTGGTTCTCC[A/G]GAGAAACATGCTGGT | 138151 |
| rs537082714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136066049 | AAATACAAAACTAGC[C/T]GGGTGTGGTGGTGGG | 138151 |
| rs537118472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012325 | CTCTCCGGGCTTCCG[C/T]AGCCCCAACGGCTAA | 138151 |
| rs537216479 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136079808 | GTAAGATTTCAGGCC[A/C]CCAGGACAGGCAGCA | 138151 |
| rs537229715 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NACC2 | GRCh38.p7 | 9:136056399 | TGTGCTCACCTCCCC[A/G]CTACTGGACATACAG | 138151 |
| rs537229760 | in-del | -/A | 0.0460142 | 0.144533 | intron-variant | NACC2 | GRCh38.p7 | 9:136034657 | GCAAGAAAATGCTTT[-/A]AAAAAAAAAAAAAGT | 138151 |
| rs537245332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136026764 | TATACAAACTTTTAA[C/T]AGGCATATACAGGGG | 138151 |
| rs537296685 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136056114 | AGGGGGCGGCAGGGG[A/G]CCCGGAGGTTAACCC | 138151 |
| rs537338661 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NACC2 | GRCh38.p7 | 9:136070364 | TGCAAAAAAATTAGC[C/T]GGGCGTGGTGGTGGG | 138151 |
| rs537383942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136021361 | GAAACGTAAAAACAC[C/T]GACGCCAAGTGCCGG | 138151 |
| rs537438646 | snp | A/C | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096554 | TGTATGGGGGTGAGT[A/C]TGGAACCCCGCAGGG | 138151 |
| rs537442098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013557 | TCCGGGGACGTCTGA[A/G]GAAGCCGCTGTGTCC | 138151 |
| rs537476269 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NACC2 | GRCh38.p7 | 9:136071005 | GAGGCTGAGGTAGGC[A/G]GATCTCTTGAGGTCA | 138151 |
| rs537512352 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009457 | CTTGGTCCCCCTGGA[C/T]GTGGGCCCTGAGGAA | 138151 |
| rs537518978 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007478 | ACGCACACACACAGA[C/T]GCACACACGCACAGA | 138151 |
| rs537525916 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NACC2 | GRCh38.p7 | 9:136089149 | GCACTGCAGCCCGGG[A/G]GAACCAGCGGGGCGG | 138151 |
| rs537556743 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014030 | TAGGGTCCGAAGAGG[C/T]GCACAGATGGGTGAG | 138151 |
| rs537597996 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136093491 | GCTCCTCCCCGCCTT[A/C]CCGCCAGGCCAGGGC | 138151 |
| rs537633759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136058941 | GCGCTGCCCCTGGAT[A/G]GGTAGCAGAGGCCCA | 138151 |
| rs537633865 | in-del | -/T | 0.125449 | 0.216765 | intron-variant | NACC2 | GRCh38.p7 | 9:136089772 | TATTTTCTTAAAAGC[-/T]TTTTTTTTTTCTTTT | 138151 |
| rs537633895 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136042773 | ACACACACAGAGACA[C/T]ACAGACACACACACA | 138151 |
| rs537694008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136058278 | ACAGGGCAGACACCC[A/G]CAGCACCTCATGGCC | 138151 |
| rs537728247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136082728 | CCCTCAATCCAGCGT[A/G]TGCACCATCAGATCA | 138151 |
| rs537729568 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136080755 | CGTGGAGACGGGGGG[C/T]CGTGACACACACCCA | 138151 |
| rs537768131 | in-del | -/TCA | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136056493 | CTGGGTGGTCTCTGG[-/TCA]TCAAGTCACAAGAGC | 138151 |
| rs537775493 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NACC2 | GRCh38.p7 | 9:136086517 | GCCCCCAGCTTCCCG[A/G]CAGCCATCTGCCTGC | 138151 |
| rs537782493 | snp | A/G | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012279 | CAGCCTTGGCCGTCC[A/G]CCAGCTGTGAGGCTC | 138151 |
| rs537783150 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136084894 | GCAGGCCTACAGAGA[C/T]AGGAAGTAGAAAGGT | 138151 |
| rs537822454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136078272 | GCCAGCCCCACTCGC[C/T]TGCAGGCCAGAAGAC | 138151 |
| rs537835878 | snp | A/C/T | 0.00755907 | 0.0610114 | intron-variant | NACC2 | GRCh38.p7 | 9:136070493 | GCCTGGGCGACAGAG[A/C/T]GAGACTCGTCTCAAA | 138151 |
| rs537846644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136024866 | GTGGAGCAGCTGAGG[C/T]GGCAGGGCCTAAAGG | 138151 |
| rs537859159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136030345 | CCGGGCGCGGTGGCT[C/T]ACGCCTGTAATCCCA | 138151 |
| rs537864281 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136024177 | GTGTGTGTGTGTGTG[A/T]GAGGACGGAGTGTGT | 138151 |
| rs537877962 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136073457 | TAATAAAAAATAAAA[A/T]ATGAGGACCCCAGTA | 138151 |
| rs537884661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067634 | CGAGGTCAAGAGATC[A/G]AGACCATCTGGCCAA | 138151 |
| rs537935825 | in-del | -/GGATTTCCACTGTCTGAAACGG | 0.00597247 | 0.0543191 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136006623 | CCTTTTGTTTGTCAT[-/GGATTTCCACTGTCTGAAACGG]CTCTGAGCACGCTTG | 138151 |
| rs537957310 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136074215 | CAGCACTTTGGGAGG[C/G]CGAGGAGGGCAGATC | 138151 |
| rs537992696 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136086618 | ATGACATGGACTCAC[C/T]GCCTAAACTGGGTTA | 138151 |
| rs537994000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136091685 | GTAAACAGCAAACGC[A/G]GGAAGGCCACAGCTG | 138151 |
| rs538057218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136091337 | GAGGACGGGTTCCTC[A/G]CTCAAGGTCACACAG | 138151 |
| rs538058367 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136091619 | TTCACGCCTGCCCAC[C/T]GCGCTCTGCTGAGAC | 138151 |
| rs538091476 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136063890 | CTCCATCTCAAAAAA[A/C]AAAAAAACAAAAAAA | 138151 |
| rs538113087 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136059885 | AACCCCTCCACCCTA[A/C]CTCAATTGCAGCCAA | 138151 |
| rs538169406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136069764 | TTAAAGCATCAATCC[A/G]CTAAGACACAGCAAT | 138151 |
| rs538171636 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136088553 | GGGCACTTGGGGCTC[A/G]TGGGGACCCAGGTCC | 138151 |
| rs538181085 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136064710 | CTTTGCCAACATTGT[C/T]GAGCTGATGCTAAAA | 138151 |
| rs538181746 | in-del | -/AC | 0.426201 | 0.177351 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007545 | GACGTGCACACACAG[-/AC]ACGCACACACACACA | 138151 |
| rs538204380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136083121 | GAGGGCCCTCTTCCT[C/T]GATGCCAGAAACGGG | 138151 |
| rs538219411 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136084846 | CACACGAGGACACCC[C/G]CTGTGGGACTCCACT | 138151 |
| rs538230984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136030764 | CCTCCCAGGTTCAAG[C/T]GATCCTCCCATCTCA | 138151 |
| rs538249494 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136033017 | AGCAAGATTCCATCT[A/C]AAAAAAAAATAAGTT | 138151 |
| rs538297091 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136018900 | CCAACAGAAATAATT[-/C]CCCATCCACAACCAC | 138151 |
| rs538346199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136078732 | AGCTGAGCAAAGCGA[A/G]CCCCTCAGGCAGGGC | 138151 |
| rs538383619 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136057616 | GGCATAGTTTAATAA[C/G]TTAAAAAGCCAGCGC | 138151 |
| rs538384499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136028221 | ATCTCCAAAAAAAAA[A/G]AAAAAAAATTGACAC | 138151 |
| rs538436458 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015137 | GAGGAGCTCATAAAC[A/T]GAAGCACGTCTCCAA | 138151 |
| rs538473162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136019800 | CCAGAAGGAGCCCCC[A/G]CCGTACCTTCCAGGC | 138151 |
| rs538481748 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136071490 | GGAGGTTGTACTGAG[A/C]TGAAACCATGCCAAT | 138151 |
| rs538509583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067305 | TTGTTGCCTAGAGCC[A/G]GGAGCAGTGGGGGTG | 138151 |
| rs538544890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015391 | GGTGGGCCCCTACCC[C/T]TCCTGGCCAGGGCAG | 138151 |
| rs538559756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136072009 | TCGGGAGGCCCAGGT[A/G]GGTGGATCACCTGAG | 138151 |
| rs538576297 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136093963 | CAGGAGCCTGCCAGA[A/C]GAAAAGAGGGGTGGG | 138151 |
| rs538619161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136027315 | CAAATGATAGAAAGA[A/G]ATGTACCAGGTAAAT | 138151 |
| rs538635188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136032405 | AAACCCTCTTAACCT[A/G]GGAAATGAAATAAAT | 138151 |
| rs538642643 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008092 | TGCTGACCTCTTGCC[C/T]ACAGCTTTGTCCACA | 138151 |
| rs538660998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136094412 | TGACCTCCGACCCCA[C/T]ACGATCCCAGCAAGA | 138151 |
| rs538736318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136086020 | GCGCAGGGCAGCTCC[A/G]ATGGGAGGGGTTGGC | 138151 |
| rs538749155 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009900 | GAAGATGGGGAAGCC[A/G]AGTTCTGGAGGGACA | 138151 |
| rs538805571 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136037485 | ATGAACATGTGCATA[C/T]GTGATTTTGTATGCA | 138151 |
| rs538850954 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136029447 | CATTTTCCTGGATGC[A/G]GAACAAGAACTCGGG | 138151 |
| rs538852200 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136022299 | TGCAGTGGGCCTCGG[A/G]GAGATGACCACACTC | 138151 |
| rs538860008 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136086990 | ACAGATATCATTAGT[A/G]AAAGGTAAGATGAGA | 138151 |
| rs538886613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136062081 | GCCGAGATTGCACCA[C/T]TGTACCTGTACTCCA | 138151 |
| rs538893174 | in-del | -/T | 0.0123036 | 0.0774623 | intron-variant | NACC2 | GRCh38.p7 | 9:136024056 | TGTGTGGGGACAGCG[-/T]TGTGTGTGTGAGGCC | 138151 |
| rs538896251 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007807 | TTCCCTTTGAGGGGA[G/T]CCCAGGCAGTACACG | 138151 |
| rs538932354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012394 | CACCCCTCCCCGTCC[C/T]AGTCCCAGCCTGGAG | 138151 |
| rs538945280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136017660 | GGTGGACACCAGTCC[A/G]GCACTCCTCACACCC | 138151 |
| rs539003453 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136057845 | GTGGAAGCGGTCGGA[G/T]CCCAGGCACCGACAG | 138151 |
| rs539079958 | in-del | -/AA | 0.00953873 | 0.0683987 | intron-variant | NACC2 | GRCh38.p7 | 9:136092114 | GCCCAGTGGGGAGAC[-/AA]GAGTAGAGAAACGCT | 138151 |
| rs539083881 | in-del | -/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136093021 | CCACTGACGGTGGCT[-/G]GGGCCACTGGGCACT | 138151 |
| rs539103177 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NACC2 | GRCh38.p7 | 9:136035608 | ATATTGAGACAACTG[A/G]AAAAAGGTACAGTCT | 138151 |
| rs539110122 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136055065 | CTGTGGTGTCGGAGT[G/T]GGGGGTCTCTCCTCT | 138151 |
| rs539128890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136046788 | AGGGAGGAGAGGCAC[A/G]AGACAGACACCGCAT | 138151 |
| rs539161842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136085607 | AGGAGGGGCCTGGGA[A/G]GCGGCTGCCAGGGGG | 138151 |
| rs539187660 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136092714 | AGAGTCAGGGGGCCC[C/G]ATAGTCAAGTTCCCA | 138151 |
| rs539228372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136028952 | GATGTTGGGCACCGT[C/T]GAGCACAAGAGGGAG | 138151 |
| rs539350773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136077248 | AGGCAGGAGAATTGC[C/T]TGAACCCGGAGGTGG | 138151 |
| rs539393629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136060138 | AATTAAAGGAAGTAC[A/G]GATAATGTAGTAAGA | 138151 |
| rs539401625 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136021184 | TCTCGATACTCAACA[G/T]TTAAAAACCAACAAT | 138151 |
| rs539404505 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010503 | CCTGGCCCTGGGCGG[A/G]GGAGCAGGGGGACGC | 138151 |
| rs539420891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136059851 | GTCAGAGTCCCTACC[C/T]CGCCGTCAAAAGGAC | 138151 |
| rs539447861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015605 | ACAGGACAGGGCTAC[A/G]CAGAACTGCTCAGGC | 138151 |
| rs539496473 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136088050 | CCTGGAAGACGGGCA[A/C]CCCCAGTGGCTGTCA | 138151 |
| rs539502634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136060241 | CCAAATCTCCCAAAG[C/T]TCTTTTGCAACACCG | 138151 |
| rs539594343 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136083589 | ACGCGGACACCTGTG[A/T]AGAGCGCCGTGCAGA | 138151 |
| rs539608955 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136031630 | GGTGTGAGCCACTGT[G/T]CCCGGCCCACGGCCC | 138151 |
| rs539634443 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NACC2 | GRCh38.p7 | 9:136017237 | CCTGCAGCTGTGCAG[C/T]GCGACCCCGATGGCA | 138151 |
| rs539643330 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136068372 | GGCATAGTGGTGTGT[C/G]CCTGTAATCCCAGCT | 138151 |
| rs539683636 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136061089 | GTGGCTAGGGGAGGA[C/G]GAACAATGCCAGGTA | 138151 |
| rs539700511 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136020312 | TCTGAGGTGCTCCAC[A/G]TCCTCACCAGGCAAA | 138151 |
| rs539733795 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136075325 | GGCTGGGATACTTGG[G/T]GGGAAAGCCCTCCCT | 138151 |
| rs539772178 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136020018 | GAACGGGGAGGGACC[A/G]TTTCATGGGGATGAG | 138151 |
| rs539792251 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007440 | ACACATACACACAGA[C/T]GCGCACACACACGCG | 138151 |
| rs539815119 | snp | A/G | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096668 | GCCACTTCCAAACCC[A/G]CCCCGCAGTCTACTG | 138151 |
| rs539847083 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012659 | CTCACAAGGTTTTTT[G/T]TTTTTTTTTTTTTTC | 138151 |
| rs539869584 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136033232 | TGCAGGTAGACTCTC[-/A]AGAGTAAATCAGTGA | 138151 |
| rs539875824 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136065899 | AAAGAATACCATAAA[C/G]AAAGTAAAAAGAGGC | 138151 |
| rs539888871 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136067641 | AGAGATCGAGACCAT[-/C]CTGGCCAACATGGTG | 138151 |
| rs539894081 | snp | C/T | 0.000798403 | 0.0199641 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011561 | CCTCCGGGCCGCGGC[C/T]GCCGGCGTCTGGGGC | 138151 |
| rs539933579 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015907 | CCGCCTTGACTGCTG[C/T]TGCCACTTGGAACCT | 138151 |
| rs539935701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136070234 | AAATACGGGCCGGGC[A/G]TGGTGGCTCACGCCT | 138151 |
| rs539952842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136062317 | GGATGCACCTTTGAC[C/T]TGCCATCTACCCGGA | 138151 |
| rs539956812 | in-del | -/GTGC | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136024288 | GTGTGAGGACAGAGG[-/GTGC]GTGTGTGTGAGGACA | 138151 |
| rs539961069 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136072526 | ATCCAGCCTGCACAA[C/T]AGGGCAAGACTCTGT | 138151 |
| rs539991487 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136093398 | CCCTTCCAGCAGCCG[G/T]TGGTAAAGAACAGAG | 138151 |
| rs540004400 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136085759 | CTGTAAGTTTAATTA[C/G]TTTATCTTTTACCTT | 138151 |
| rs540033182 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136035989 | AATTTCTTTAAATAG[C/G]ATATAAAAACTGCTA | 138151 |
| rs540080914 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136057327 | CAAACACAGCACAGA[C/G]TGTCAACAGGGATGG | 138151 |
| rs540123274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136081742 | CCCTGGGGCACCATC[C/T]CCACCAAGTGGCGGC | 138151 |
| rs540168430 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078216 | TGCATACCCACCACC[A/T]GGCAGGGGTCCCCAG | 138151 |
| rs540174052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136081312 | TAGAGTAACCGGAAC[A/G]ACCTGCACACCACAC | 138151 |
| rs540176401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136088971 | ATGATCTCGGCATCG[C/T]GTGGAGCGGCTGAGG | 138151 |
| rs540183894 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136055767 | AGAGAGGCGGGGCAC[A/G]GGAAACGTTCTGCGG | 138151 |
| rs540187044 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136038352 | ACCAGCCTGGGCAAC[A/G]TGCTGAAATCCTGTC | 138151 |
| rs540265549 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136075003 | GGGGGAACAGCAATC[A/G]GATCCTCACGAAACA | 138151 |
| rs540277404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136056936 | ATCAGCCCTTCCTCT[C/T]GGCCACCCGTGGGCA | 138151 |
| rs540279008 | in-del | -/TT | 0.491936 | 0.0629843 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012653 | ATTTGCCTCACAAGG[-/TT]TTTTTTTTTTTTTTT | 138151 |
| rs540305054 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008230 | GCACCCAGCCAGGCG[C/T]GGCCCGCCGGGCTCA | 138151 |
| rs540334446 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013119 | GCCGGGAGCACCCCC[A/G]CGGCCCACCCAGTCC | 138151 |
| rs540336425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067429 | ACTCTGAATACAGAC[A/G]TGTTGATTAACGACG | 138151 |
| rs540340071 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007872 | ACAGTTTCAGCTGTC[A/G]AATGAGGACAGGTCA | 138151 |
| rs540357322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136094614 | CCCAGTTTCTCCCCA[A/G]GCTGGGGCCCGAGTG | 138151 |
| rs540388659 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136019373 | GAGCAAGGAAGAGGC[A/C]CCTGCCGGTCACACT | 138151 |
| rs540415326 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096481 | TTAGGTTCTATTCAG[C/G]TCTGCGTCCAGAACA | 138151 |
| rs540427451 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136095713 | AGCCCCCGGGCCCCC[C/T]TACCCCGCCCCCGGC | 138151 |
| rs540442966 | snp | C/T | | | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015981 | GGGGACTGGCAACTA[C/T]ACGTGACATGGTTTT | 138151 |
| rs540483829 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136038245 | CTATACGTATTTTTT[C/T]AAACACCAGGCTGGG | 138151 |
| rs540499215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136029051 | ACAGGCTCCTGGATG[A/G]AAAGGGGTGGGTCCT | 138151 |
| rs540506544 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013661 | CATCCACAAGCCCGT[C/T]TGAGAAAGGCCACGA | 138151 |
| rs540569427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136086128 | AGAAAACCAAGTCAC[C/T]CCTGGGGACCCTTGT | 138151 |
| rs540580613 | snp | C/G/T | 0.00239393 | 0.0345281 | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014047 | CACAGATGGGTGAGG[C/G/T]GGAGGGGGGGAGGTG | 138151 |
| rs540621178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136023944 | ATGCCCCCAACCACA[C/T]AAATGCACAACCCCC | 138151 |
| rs540635273 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136023535 | TTATCTCCTGCAAAT[C/G]CCAGCACCCACTCCT | 138151 |
| rs540709623 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136073699 | ATACCTGGAAATAAG[G/T]AGTATGAAAAGCAGC | 138151 |
| rs540752954 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136018201 | CCTGTTCCCAGTCCC[A/T]CCATGACCCCCACCT | 138151 |
| rs540818698 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014048 | ACAGATGGGTGAGGG[G/T]GAGGGGGGGAGGTGG | 138151 |
| rs540819349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136016052 | TGCCAATCAGGAATG[C/T]GACCAGCCCAGGGGA | 138151 |
| rs540849483 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136067989 | AAGCATTTGTGTATC[A/G]AAACATAGTAAAGGT | 138151 |
| rs540858323 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136093031 | TGGCTGGGGCCACTG[C/G]GCACTCGGTGCCCTG | 138151 |
| rs540880731 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136021408 | CTGGGACGTCCTGAC[G/T]ACGTGGTCTCACCTC | 138151 |
| rs540907351 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136079567 | GACACGAAGGAACAG[A/C/G]CTGACTCACTGAGTG | 138151 |
| rs540942857 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136063565 | TTTCCTACCTGGGAA[A/G]GGTATGCACAAACAA | 138151 |
| rs541017974 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007524 | ACGCGCACACACAGA[C/T]GCACAGACGTGCACA | 138151 |
| rs541028875 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NACC2 | GRCh38.p7 | 9:136025630 | AAAAAAAAAAAAAAC[C/G]CAGCCGGGCGCAGTG | 138151 |
| rs541029694 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136025830 | GGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 138151 |
| rs541042395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136056234 | TTTTAAAATGCCAGA[A/G]AGCAGAGCTGGGCTG | 138151 |
| rs541054703 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007113 | GCTAAAAATAGTATT[A/G]CAAGTTTTGGCTTCT | 138151 |
| rs541123512 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136075454 | GCCTGTTTCCCTTTC[A/G]TAGACGTCGGCAGCG | 138151 |
| rs541145739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136020805 | CCACATGGCCATGCT[C/T]GATTGGCTTTTGACA | 138151 |
| rs541256701 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015688 | GGGAAGAAATCCCCA[C/G]AAAATGGCCCAATAG | 138151 |
| rs541284176 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136061236 | GGAGGGACAGGCCAG[C/G]ACTCCTGACACCCCA | 138151 |
| rs541351468 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136022384 | CTCCTGCCCGATGCC[C/G]AGCAAGGCTGGGACC | 138151 |
| rs541451339 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008978 | AGTGAGGAAGGGGCA[C/T]GGGACATTGTGCGGG | 138151 |
| rs541465928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136087714 | CTTCCACCGCAGCAC[A/G]GGGGGAAATGAGGCT | 138151 |
| rs541479771 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136061698 | CAGAAAGAGGCAGAT[C/T]GGAGGTCTAGCAGGC | 138151 |
| rs541483392 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136091044 | CACTGGGGGAGGGGA[G/T]ATTCCTTTAGAGAGA | 138151 |
| rs541503403 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136066085 | GTAACCCCAGCTACT[C/T]GGGAGGCTGAAACAG | 138151 |
| rs541524559 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136080447 | CGTGGTGGCGCACGC[C/T]TGCAATCCCAGCTAC | 138151 |
| rs541528608 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136031386 | TCCATCACCCAGGCT[-/G]GGGTGCAGTGGCACA | 138151 |
| rs541554365 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136058157 | TAGGCCCTGGCTGGC[A/G]AGGGGGCTGCTGGCA | 138151 |
| rs541610916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136030370 | ATCCCAGCACTTTGC[A/G]AGGCCAAGGCAGGCA | 138151 |
| rs541610981 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136024559 | GTGAGGACAGTGTGT[G/T]TAAGGACAGAGTGTG | 138151 |
| rs541612261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136080824 | AGACGGCAGATGACC[A/G]CAGGCCGGCCTGTGC | 138151 |
| rs541626308 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136077962 | TCTTTTTAGTAGAGA[A/C]GGGGTTTCACCATGT | 138151 |
| rs541693921 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136024900 | CAGTGGCTGACAGAG[C/G]CGGGAGCCTCGGGGC | 138151 |
| rs541727573 | snp | C/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007217 | AGTCTGAATGCTTGC[C/G]ATTCTGCATGATTTT | 138151 |
| rs541733995 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136018943 | TGTTTTTCTAAACAG[C/T]AGAAGTTGTTTGTGC | 138151 |
| rs541748007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136076658 | TGCCACTGAACTGTG[C/T]GCTTAAAAAATGGTT | 138151 |
| rs541757745 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136027872 | TATATAAATACATAC[A/G]TAAGAGAAAAAATCC | 138151 |
| rs541762650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136073918 | GTAAGCGGTGATCCT[C/T]CCCTCTGCCCTGAAA | 138151 |
| rs541807128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136086294 | GGGCACATGCCCCCC[A/G]AGGCCTCCCACTCAG | 138151 |
| rs541860812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136078729 | CAGAGCTGAGCAAAG[C/T]GAGCCCCTCAGGCAG | 138151 |
| rs541870009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136042992 | GACGCAGACACACAG[A/G]CACAGTGTTGCCCCA | 138151 |
| rs541880386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136017776 | GCAAGGCCCTGAGAG[A/G]GCCACCTGCCCAGTC | 138151 |
| rs541909750 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NACC2 | GRCh38.p7 | 9:136059341 | ATGCACCAGCCCATC[C/T]GGAGCAGGGCCCTAT | 138151 |
| rs541931257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136058401 | TCCTCAGGGGTGTCC[A/G]GCGGAAGCAGCAGGC | 138151 |
| rs541973278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015172 | ATCAGCCCCACACCC[C/T]AAACAGAGGCCACAG | 138151 |
| rs541984274 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136093770 | ACAGAGGACCAGAGG[A/G]GTGCTCCAACGGTGG | 138151 |
| rs541991209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136086710 | TAGGAAAACCCTCCC[C/T]GACCAGTGGCCCCGT | 138151 |
| rs542017664 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136082786 | TGGCTCTTGGCCAGC[A/G]GATCCCACAGACGCC | 138151 |
| rs542069860 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136078158 | AGTGGTAGAGAGTGG[A/G]ATGGACCAGGCACCC | 138151 |
| rs542095869 | snp | C/G | 0.204803 | 0.245881 | intron-variant | NACC2 | GRCh38.p7 | 9:136045587 | TGTGGGCGCAGGTCC[C/G]GGCAGCCCCCTCCCC | 138151 |
| rs542124283 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136050811 | GCTGCAGATCCCCGG[C/G]GTGCTGCCCGGCAGG | 138151 |
| rs542132959 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136057529 | ATTAAGCTGTGTTTC[A/G]AAAAGAGCCGACAAT | 138151 |
| rs542156332 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014638 | CTGGGTTTGGGAAAC[A/C]CTCATGTCTTTGCCT | 138151 |
| rs542208598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136088199 | GCTCTAAACGTGCTC[C/T]GTCCGGCTCCCTTCC | 138151 |
| rs542240036 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136097272 | GGGGTGCAGTGGCGC[A/G]ATCTCAGCTCACTGT | 138151 |
| rs542282650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014216 | GGGTGGGGAAAGCCA[C/T]AGCGCCCCCCACCCT | 138151 |
| rs542358398 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010335 | GGGGAGCCCAGCACC[A/G]GGAGGACCGACTCTC | 138151 |
| rs542371722 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136087879 | GGGCAAGCCCTCCCC[A/G]TCCCTTGTCTGCTGC | 138151 |
| rs542403879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136028529 | TACAGGTGATGGCAG[C/T]GGTGGCCCGTCTGGA | 138151 |
| rs542449233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136059916 | GACCCACCCCGATGT[C/T]CTGACCAGCAGAGAG | 138151 |
| rs542466924 | snp | A/C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010733 | TACATCAGCTGTGCA[A/C/T]GTCCCACAGTGGGCC | 138151 |
| rs542476463 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136094003 | GGGGCGACCTGGAGG[C/G]ACACGGACTCTGGCA | 138151 |
| rs542485295 | in-del | -/CA | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136080631 | CACCATCCCCCACCC[-/CA]CAGACCGCACAGAAT | 138151 |
| rs542490851 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136062152 | CAGGACAGGACAGGA[A/C]AGGACAGGACAGGAC | 138151 |
| rs542497886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136085638 | TGGGTACAGGCGGGT[A/G]GCGGGCAGCCCTCTG | 138151 |
| rs542503728 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136031247 | CAGATAATCTTGATA[C/T]CAAAACATTGGGAAG | 138151 |
| rs542521321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136081994 | GCGAGAGCCAGGCTG[C/T]AGCAAAGGCCAATCT | 138151 |
| rs542559427 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136085109 | TGAATTTATAGCCTG[G/T]GCAACATAGGAAGAC | 138151 |
| rs542566301 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136023183 | CTCCTGGAAACCCGG[A/T]TGGAAAGGGGCTCGC | 138151 |
| rs542598345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136016776 | CAGAGCCTGCTTGCC[A/G]GGCAGGAGTGACAGC | 138151 |
| rs542703526 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136061827 | AGAGCAGGCCATTAC[A/G]AAAAGTTGGTGGCCG | 138151 |
| rs542731470 | in-del | -/A | 0.0448719 | 0.142907 | intron-variant | NACC2 | GRCh38.p7 | 9:136037858 | GTAGGTTATATGGTT[-/A]AAAAAAAAAATGAAA | 138151 |
| rs542739972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136093708 | AACAGTGACCCCAGG[A/G]GAAAACGCCAAGAGG | 138151 |
| rs542811398 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136085311 | TGAACCACTGTGCCC[C/G]ACCCAAAAAAATTTT | 138151 |
| rs542842438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136056339 | GGCGGCCAGGAACTC[C/T]CCCCAACCCCGAGGC | 138151 |
| rs542872179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012482 | GCCCAGGCCAAGGCC[A/G]GGTCATTCCTCCCAA | 138151 |
| rs542891969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136017840 | CTGGGCTCCTGCACA[C/T]CCTACCGAGCGCAAG | 138151 |
| rs542902821 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136033684 | GAACTTCTAGGAATA[A/C]ATCTTTTTAAAAAAA | 138151 |
| rs542918526 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136027528 | AGTGCATTCTATGTC[A/C]ACTGGAAATTTAATT | 138151 |
| rs543034975 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136025133 | GGGTTCTGGGGAACA[C/G]CAGGCTTTCAGCTGA | 138151 |
| rs543090940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136035677 | TGAATTTTGCACAGC[A/G]TACTGTGATTATATA | 138151 |
| rs543137247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136072288 | TGGTGGCTCATGTCT[A/G]TAATCCCAGCACATT | 138151 |
| rs543158733 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136018143 | CACCTGCGGCCGCAC[C/T]GCACCAGGACGCTCA | 138151 |
| rs543166439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015275 | GCACCTGCGCCCCAG[A/G]GCCCAACCCCAGGGG | 138151 |
| rs543206904 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136020708 | TTAAGACTTCCTGTA[C/G]AGCTACAGTCATGAA | 138151 |
| rs543231212 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136046618 | GGGGCTTGAACTCGG[-/C]CCCATCAACCTCACA | 138151 |
| rs543236095 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136072923 | GAGGGGAAAGAAAAA[A/C]ACACACAAGAGAATA | 138151 |
| rs543255877 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136080532 | TGAGATCGTGCCACT[G/T]CACTCCAGCCTGGGT | 138151 |
| rs543297986 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136063172 | CGTGTGGTTTGAGCC[A/G]CATTCCCATTACGTG | 138151 |
| rs543322245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136062777 | AAAGACTTAGCCAAG[C/T]GTGGTGGTGTGTGAC | 138151 |
| rs543330133 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010886 | CCCTTTTCTCCACCC[C/T]GAGGGGTGGGCCACA | 138151 |
| rs543360123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136064975 | ACAGTCTTTTCAAAA[C/T]GTGGTGCTGGGACGA | 138151 |
| rs543411012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136093254 | GGAAGAACCGCTCAG[C/T]ACCAAGATCGTCACT | 138151 |
| rs543426339 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136031042 | AAGAGGAAATAGATT[A/C]TGTGAACTATTCCTG | 138151 |
| rs543428261 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136028331 | TACTTTAGGTAGGCT[C/G]ACCACATGTACTTTC | 138151 |
| rs543488717 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136047027 | CAATCGCTCAGGCCC[A/G]CCTCTCACTCAACAG | 138151 |
| rs543488824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136030558 | GAGCTTGCAGTGAGC[C/T]GAGACTGCGCCACTG | 138151 |
| rs543526242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136074978 | CCCACTCACTGTCGC[A/G]TATGGGGCTGGGGGA | 138151 |
| rs543533862 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136051055 | AGGGAGGGGGGTCTC[C/T]GGAGCTGTGCAGTTT | 138151 |
| rs543538104 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136066476 | CATACCCACTAGGAT[G/T]GCTATAATCAAAAAG | 138151 |
| rs543540208 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136026137 | TTGAGGTTAGGAGTT[C/T]GAGACCAGCTTGGCT | 138151 |
| rs543596351 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136081814 | CCTGGCCCAGGTAAC[C/T]AGGCAACACCAGGCT | 138151 |
| rs543609833 | snp | G/T | | | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011765 | TCTCAGAGCCACGAT[G/T]GTGGCGGCGTCGCCC | 138151 |
| rs543611612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136069442 | TAATCTCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 138151 |
| rs543644448 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136020178 | TTACCACAATAACAA[C/T]GCTCAGAAAGAACAA | 138151 |
| rs543658335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136032184 | GGGAAGGAATATCAG[C/T]GAGCTGCATCCAGAG | 138151 |
| rs543731420 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014704 | CAACGATGAGGGAGA[C/T]GGAATCCCCTGGCTG | 138151 |
| rs543746854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136070010 | ATATGTTCTTTTCAC[A/G]TGCCTGTGGAACATA | 138151 |
| rs543753319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136076248 | TCCCGGCCCTGCGGA[A/G]CTCGAAGAAGTGCTG | 138151 |
| rs543791000 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006374 | CCCCACAGCCAGATC[A/C]CTGCCCTGTTGTGTG | 138151 |
| rs543832517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136060633 | TCCCTGGCCAAGGCC[A/G]CACCCCAGCACCACA | 138151 |
| rs543842871 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136032192 | ATATCAGCGAGCTGC[A/G]TCCAGAGGCATGTAT | 138151 |
| rs543859801 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008270 | TCACACCTCCGGTCC[C/T]TCCTGGACCTCTCCA | 138151 |
| rs543862240 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136057820 | ATCATCACCACTGGG[G/T]CCGGGGGTTGTGGAA | 138151 |
| rs543868420 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | NACC2 | GRCh38.p7 | 9:136094672 | CACGAACGGGCCCAC[C/G]TGGACCGGGAGGGCG | 138151 |
| rs543899120 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013181 | CCCCACCCACCCGAG[A/C]GACCCCCAGGCTCTT | 138151 |
| rs543915954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136084341 | CCTGGGGCCTTCACC[A/G]AAGGCGGGTTGCTGG | 138151 |
| rs543921731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136057403 | GCTGGGGTGGCTCCT[A/G]TTGAGCCCCAGATCC | 138151 |
| rs543923365 | snp | C/G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136029098 | AAGCCAGGAATGGCC[C/G/T]GAAGCCCAGGGCCCA | 138151 |
| rs543965560 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136080067 | CTGTAGTCATGGCCC[A/T]GCTGGCAGAGACACA | 138151 |
| rs543979618 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136088733 | TTTCCTGACCCACTG[C/T]TTCATGCCTCCTAGG | 138151 |
| rs543981982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136026972 | AGTAGCTCATGCCTG[C/T]AATCCCAGCACTCTG | 138151 |
| rs544032465 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136081841 | GGCTGAGGGCAAGGC[A/G]GGGAGGGCAGCCAGC | 138151 |
| rs544065415 | in-del | -/GTGTGTGT | 0.0711525 | 0.174681 | intron-variant | NACC2 | GRCh38.p7 | 9:136024156 | GTGTGTGGGGACAGA[-/GTGTGTGT]GTGTGTGTGTGTGTG | 138151 |
| rs544149170 | snp | A/C/G/T | 0.00279242 | 0.0372774 | intron-variant | NACC2 | GRCh38.p7 | 9:136023980 | ACACACGTGCACATG[A/C/G/T]GTCAGACATGGAGGA | 138151 |
| rs544187417 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136095447 | GGGTCCGGGGGCCGG[C/G]AGGGTCCCCAGTGGG | 138151 |
| rs544218621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136090469 | CAGTAGGGGTGGGGA[A/G]GGAGCATCTGAAGTG | 138151 |
| rs544225560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136077551 | GCGTGTGGTCAGAGT[A/G]TGGAAAGAATTCTAC | 138151 |
| rs544262404 | in-del | -/ACAT | 0.0023933 | 0.0345097 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007373 | GACACACGCGTGCAC[-/ACAT]ACACAGACACGCGTG | 138151 |
| rs544324541 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136085836 | AGCCAGGTGGGGTAG[G/T]TCCCTCCACAATCCT | 138151 |
| rs544358549 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136091823 | GGCTGGTGAGAGCAA[C/G]GATTTGCTTAAAAAA | 138151 |
| rs544373916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136063606 | TCTCTTAAAAAGGCC[A/G]AGCACGGTGGCTCAC | 138151 |
| rs544390695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136056439 | CTGAGACCTCACAGT[C/T]GGGAGGCAGCGGGGC | 138151 |
| rs544412354 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096583 | GGACTCTGGGCTCTC[C/T]CCACAGAGTCCCATC | 138151 |
| rs544464454 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136030046 | CACCTGCTTAATTTT[C/T]GTAATTTTAGTAGAC | 138151 |
| rs544468135 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136075805 | TCTTGGGTTTGGGCT[C/G]TGAGGCTCGGGACAC | 138151 |
| rs544516758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136058586 | TAGGAACAACAGGAT[A/G]AGGGAGGGAAGAGGG | 138151 |
| rs544548757 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136032508 | CTTTTCCTGAGTTTA[C/G]AAATGAGACAGGGAT | 138151 |
| rs544572693 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136080487 | TGAGACAGGAGAATT[C/G]CTTCAACCTGGGAGG | 138151 |
| rs544573027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136018844 | TGTGATTACACACGC[A/G]GAGAAGCCGCACGGT | 138151 |
| rs544577744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136075698 | GCCCGGTCTTCCACA[C/T]GCGGGGAGGACACCC | 138151 |
| rs544684517 | snp | C/T | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136026902 | CAAAGTCAGTAACCA[C/T]GTGAAATGAAAGTCA | 138151 |
| rs544796419 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136093664 | CTCCTTTTATTTCCT[C/T]CCCTTGGACTCTGGC | 138151 |
| rs544821744 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136064193 | ACTCAGGAGGCTGAG[C/G]GGGGAGAATCACTTG | 138151 |
| rs544881333 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136045411 | TGGGAAAGGGTTACC[A/G]TGGAAGTGTGCAGCT | 138151 |
| rs544914108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136059280 | CACACGCACAGGGGC[C/T]CGCAGAGCTAAGCAA | 138151 |
| rs544981130 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007559 | GACACGCACACACAC[A/G]CAGACACGCGCACAC | 138151 |
| rs545013175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136021430 | TCTCACCTCCCAGTG[C/T]GGCGAAACATAAAAA | 138151 |
| rs545057480 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136033419 | GAGGCTGATGTGGGC[A/G]GATCATCTGAGGTCA | 138151 |
| rs545141456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136028582 | CTGTAGTGGGTGAGG[C/T]GTGGCCAGGGCTGCA | 138151 |
| rs545144907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136016097 | TAAATTAATTCAATT[A/G]AATAACTTCTCTTAA | 138151 |
| rs545145974 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136032269 | TACGAAGTTATTTCA[A/C/G]TATTTGGAAAAGCAG | 138151 |
| rs545184747 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007189 | GACTGATCGGAATAC[G/T]AGCCGGTCGTCCAGT | 138151 |
| rs545191512 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136089119 | CCAGCTTTCAGTTAC[A/G]CGGTTACGTTTGCAG | 138151 |
| rs545191555 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | NACC2 | GRCh38.p7 | 9:136072470 | GAATTGCTTGAACCC[A/T]GAAGGCAGAGATTGC | 138151 |
| rs545203715 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136022576 | GGTCCATGGTCCCAG[A/C]TCGCTGCCTCCTGGC | 138151 |
| rs545244977 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136069994 | TCAACAACAGCAGAA[C/T]ATATGTTCTTTTCAC | 138151 |
| rs545257216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136016669 | CACAGGGAAGCTCTT[A/G]TGAACGAGTGAGCAG | 138151 |
| rs545259471 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136061334 | CATGGCGGCAGCTCC[A/G]TTTCCCGGGCACTCA | 138151 |
| rs545340684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136080564 | ACAACAGCGAAACTC[C/T]ATCTCCCCACTACCC | 138151 |
| rs545341651 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136020402 | CCTGTTCCTGTCCCC[-/A]AGGCAGAGTGTGTCA | 138151 |
| rs545355929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136068224 | ATTGTGTGGCTGGGC[A/G]CAGTAGCTCATGCCT | 138151 |
| rs545367420 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136027587 | AAAATCCAAAAAGGT[G/T]TGTAAATTAAGCAGT | 138151 |
| rs545434989 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136082524 | CCTCATCTCAACGGG[G/T]TCACCATCCATGAAG | 138151 |
| rs545496288 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136086731 | GTGGCCCCGTTTCCC[C/T]CCCACGACCCCCGCT | 138151 |
| rs545522511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136043114 | CACTAGCCGTAAAAT[A/G]CAACTTTAATAAATT | 138151 |
| rs545528240 | snp | A/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010669 | AACCTAAAAAAAACA[A/T]GACAAGCATAATCCC | 138151 |
| rs545551838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136019458 | ACCCCAGGACTGGCC[A/G]CTGTAGCAGAACTGC | 138151 |
| rs545584424 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136025447 | ATAAAAAACAAAACA[A/G]AACAAAACAACAAAA | 138151 |
| rs545591052 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136076987 | CTCCAGCCTGGGCGA[C/T]AGAGCGAGACTCTGT | 138151 |
| rs545598532 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136025029 | AAAATCAACTGCCAA[A/G]AAACGAAAAAAACAA | 138151 |
| rs545627656 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136028077 | CCAGCCTGGCCAACA[C/T]GGTGAAACCCCCATC | 138151 |
| rs545691650 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136067179 | GAATCGCTTGAACCC[A/G]GGAGGCGGACGTTGC | 138151 |
| rs545704085 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012720 | TCTTGGGCCGAGGGC[A/C]ACAGGAGGCTGTGCT | 138151 |
| rs545713309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136020144 | AAAAGTCACTGCAAC[A/G]GCCCCTCTCACGTCC | 138151 |
| rs545734567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136087228 | CCAGCCCTGAAGATG[C/T]ACAGAGTGTCAACTC | 138151 |
| rs545788519 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136068810 | AAAGAAACAAAAGAT[A/G]GAACAGAATCAAAAA | 138151 |
| rs545800585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014714 | GGAGACGGAATCCCC[C/T]GGCTGGAGGGTATGG | 138151 |
| rs545804362 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136055911 | GGTGTGGGGATGGGG[C/T]GGGCCTGCTGTGCCA | 138151 |
| rs545823195 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136018962 | AGTTGTTTGTGCTTG[C/G]AACACCCGCCCCTCC | 138151 |
| rs545850862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136047732 | GGGACTCCACAGAGC[C/T]GCTTCCTGGCTGCGG | 138151 |
| rs545858090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136059198 | ACCCAGTGAGCCCAG[A/G]AGCAGGGCCATTCCC | 138151 |
| rs545901235 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136078442 | AATGGCAATCCTTAA[A/T]ACAGGTTTTTCCATT | 138151 |
| rs545969658 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136056282 | TAATGGAACCACCAG[C/T]TCCATGCAGATGAGA | 138151 |
| rs545983223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136078951 | GATGCCCTTAGCACC[A/G]TCGCCGGCATGATGC | 138151 |
| rs545995349 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136074613 | CCATTCCTCGTTCTG[A/T]CACAGCAAGGCTGCC | 138151 |
| rs545996600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136065529 | GGTGGTTGAGGCAGG[A/G]TAATTGCTTGAACCT | 138151 |
| rs546028932 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | NACC2 | GRCh38.p7 | 9:136051029 | CGCGCTGGAGCAGCG[A/G]GGAAGGAGGGAGGGA | 138151 |
| rs546032977 | snp | G/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007878 | TCAGCTGTCGAATGA[G/T]GACAGGTCAGGGTCA | 138151 |
| rs546077341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136069409 | CAAAAATTAGCCGGG[C/T]GTGGTGGCAGGCACC | 138151 |
| rs546112224 | in-del | -/G | 0.00755907 | 0.0610114 | intron-variant | NACC2 | GRCh38.p7 | 9:136059049 | GAAGGTGCTGGGTCA[-/G]GGGCAGGGGAGAAGC | 138151 |
| rs546131207 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136074931 | AATGGGTTCTCGCAC[A/G]GCCTCCTTCTGGGAG | 138151 |
| rs546173692 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010753 | CACAGTGGGCCCGGG[C/T]GGGACAGTGGGAGGC | 138151 |
| rs546212452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015267 | CCGCGTGGGCACCTG[C/T]GCCCCAGAGCCCAAC | 138151 |
| rs546212914 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136092549 | GGAAGCCCAGCCCCA[C/G]GTTTCCTCAGCCCAG | 138151 |
| rs546214369 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136064803 | TTAGAGCAGTCATAC[C/T]TCCCAATTTCTGCTA | 138151 |
| rs546216490 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136061860 | CGCGGTGGCTCACAA[C/T]TGTAATCCCAGCACT | 138151 |
| rs546246666 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136092039 | AAACGAGATCCACCT[C/G]GGGATTAGGGGGCGC | 138151 |
| rs546330451 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | NACC2 | GRCh38.p7 | 9:136083683 | GCTGCGGAGGCAGGC[A/G]GGGGCCCCGAGACAC | 138151 |
| rs546332063 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136032926 | GGGAGGCTGAGGCAG[A/G]AGAATCACTAGAACT | 138151 |
| rs546357220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136031853 | GGCTTTTACTGCTGC[C/T]TCCAGGCCCTGGCTC | 138151 |
| rs546395213 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NACC2 | GRCh38.p7 | 9:136056356 | CCCAACCCCGAGGCC[C/T]CCACAAAAGCCAGGA | 138151 |
| rs546402681 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136080680 | TCCACGGAGCTCTTG[C/T]TTATCTGATTTGGAG | 138151 |
| rs546405665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136084815 | TGGGGAGAGGGTGCG[A/G]AGCAAATGAGCCAGT | 138151 |
| rs546444751 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136026277 | ACCCAGCGGGGGTGG[A/G]GGTTGCAGTGAACCA | 138151 |
| rs546539332 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136076866 | ACAAAAAAAATTAGC[A/C]GGGCGTGGTGGCGGG | 138151 |
| rs546565639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136084543 | AAACTGGCCCAGACC[C/T]CGGAGTCAGGGTCAC | 138151 |
| rs546575876 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136088968 | ATAATGATCTCGGCA[A/T]CGCGTGGAGCGGCTG | 138151 |
| rs546580738 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011045 | TTAGGCCCTGGAGCC[C/T]GAGCCCTGCCCCGTC | 138151 |
| rs546617794 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007667 | GCTGAGGACAGCTAC[A/G]AGCTCTGGATTCTGC | 138151 |
| rs546619748 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136093723 | GGAAAACGCCAAGAG[G/T]CCTCTTTAAGGGAGG | 138151 |
| rs546636481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012898 | AGGCTCAAAATAACC[A/G]CAAAATGTAAATAAG | 138151 |
| rs546642223 | snp | A/G/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009860 | GGGGTGCTGATGGGC[A/G/T]CAGGGCTGCACTTGT | 138151 |
| rs546657967 | snp | C/T | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136094783 | CCTGCCCCGGCTTCC[C/T]CACCCGGAGGGCTGG | 138151 |
| rs546780025 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136091119 | CTGGAGAAAAGCCTG[A/C]CTCTTGTTCTCCCGG | 138151 |
| rs546792720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136061597 | TCGGGGGTTGAGACC[C/T]TGTGCGGCTCACACC | 138151 |
| rs546795132 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136028695 | CAGGCGCAGCTGCAG[C/T]TGCCCAGCTGTGGCT | 138151 |
| rs546796924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136022256 | ACGGGTGACCAGGCC[C/T]GGGTGATGAGGTAAC | 138151 |
| rs546858227 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136028147 | GTGCCTGTAATCCCA[C/G]CTACTTGAGAGGCTG | 138151 |
| rs546867681 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | NACC2 | GRCh38.p7 | 9:136086005 | CAGAGACTGGGCACC[A/G]CGCAGGGCAGCTCCG | 138151 |
| rs546879796 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136090702 | GGGACTTTTATTTTC[A/C]ATCAACAAACATTTC | 138151 |
| rs546882960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136022833 | TCATGTGCCACAGGG[C/T]AAAGGTGCCACCAAT | 138151 |
| rs546946859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136072377 | ACAGTGAAATCCTGT[C/T]GCTAATGAAAATACA | 138151 |
| rs546971451 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136046425 | TCTCCCGAGGCTGCC[A/G]GCCACAGGGCCAGGA | 138151 |
| rs546972314 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136092893 | CCACTGCGTGACCCT[A/G]CAAAGGGGATGGAGT | 138151 |
| rs547014667 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136056673 | GGGTCTCTGGGATGA[C/T]GGGCCCCCTCGGACT | 138151 |
| rs547085653 | in-del | -/AAAAC | 0.0660681 | 0.169319 | intron-variant | NACC2 | GRCh38.p7 | 9:136069549 | GTGAAACTCTGTCAA[-/AAAAC]AAAACAAAACAAAAC | 138151 |
| rs547087284 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136088311 | GGGGGCAGGGGACAC[A/C]CTGTACTCAGCAGGG | 138151 |
| rs547092669 | snp | A/G | 1.71956e-05 | 0.00293215 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013341 | GTGAGGATGATGGGG[A/G]GGGTACCTGGAGGCG | 138151 |
| rs547127977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136082441 | AGGTGTGCACAGGGC[C/T]GAGCTGATGGTGGCC | 138151 |
| rs547141562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136092156 | CCCCACCCAAGGCCC[A/G]ACTGCCCACCTCTGG | 138151 |
| rs547227135 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | NACC2 | GRCh38.p7 | 9:136042343 | ACAACCTGACTTCAA[G/T]AATTAAAGCTACAGT | 138151 |
| rs547268370 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136061572 | TACCCAAGAGGATGC[A/G]TGTACACGTTCGGGG | 138151 |
| rs547329227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014965 | GCAGCCAGTCTCAAT[A/G]ACCATGAGATGTCAT | 138151 |
| rs547330610 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136052927 | ATCCTGGGCTCATAC[C/T]AGCCTCTCTGCGTGG | 138151 |
| rs547345635 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136081488 | GAAGGCGGTGCCGGG[A/C/T]GTCCGCTTCCACCTC | 138151 |
| rs547366577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136026604 | AGACAGTGAAAAGCA[C/T]GGGGAAAAAATGTGC | 138151 |
| rs547511184 | in-del | -/AAG | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136072549 | GACTCTGTCTCAAAA[-/AAG]AAAAGAAAAGAAAAA | 138151 |
| rs547517330 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136031955 | GCTGTTAACAGCTTT[C/G]CCGATGCTAGGGCCT | 138151 |
| rs547518320 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136064609 | CCTAACATTATTAAA[C/G]TCTTCCTTAATAATG | 138151 |
| rs547549898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136065850 | AAAACCCAGATACAT[C/T]AGACTTCCTCAAAAT | 138151 |
| rs547560795 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136088018 | CTGGGGACTCTGCTG[A/G]GAAGTTCCAGAGGTG | 138151 |
| rs547606622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136022242 | TGGGGGCACCACAGA[C/T]GGGTGACCAGGCCCG | 138151 |
| rs547674719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136061534 | GGGGTAGGGGAAGGC[A/G]GATGGATGGGCCGTG | 138151 |
| rs547688305 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136048922 | ACCCAGGCCCAGGCC[A/G]CTGCACACAGGCCCT | 138151 |
| rs547742858 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136084896 | AGGCCTACAGAGACA[-/G]GAAGTAGAAAGGTGC | 138151 |
| rs547789334 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136023846 | GTGTGCTGAGAAGGA[C/T]GACCAGGACACTAAG | 138151 |
| rs547797219 | snp | G/T | 0.000399281 | 0.0141238 | missense | NACC2 | GRCh38.p7 | 9:136011807 | GTAGATGCGTTGCTC[G/T]AACACCTGTGCCGCG | 138151 |
| rs547822587 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | NACC2 | GRCh38.p7 | 9:136037796 | TTACAGGCATGAACT[A/G]CTGTGCTTGGCCAAG | 138151 |
| rs547826031 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136079263 | GAGACCAGGGAGAGG[C/G]AGGGCACTTGCCCAG | 138151 |
| rs547919352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136075552 | CAAGCCCAGGCTGTC[A/G]TGCCTGAGGACGCAT | 138151 |
| rs547983254 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136063899 | AAAAAAAAAAAAAAC[-/A]AAAAAAACAAAAATC | 138151 |
| rs548007813 | in-del | -/T | 0.117491 | 0.211994 | intron-variant | NACC2 | GRCh38.p7 | 9:136089772 | ATTTTCTTAAAAGCT[-/T]TTTTTTTTTTCTTTT | 138151 |
| rs548068455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136063265 | GCACCTGGGAGCAAC[A/G]CACCAGCGAGGGGGC | 138151 |
| rs548072477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136093380 | GCAGAGCAGCCCTGC[A/G]AACCCTTCCAGCAGC | 138151 |
| rs548081095 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136067784 | AGGTTGCGGTGAGCC[A/G]AGATCGCGGCACTGC | 138151 |
| rs548132979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136017985 | CGGCATGGTCCCCTC[A/G]GCAGCCTCAGTGTGA | 138151 |
| rs548151538 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136095976 | GCGCACTGGGGCGTT[A/G]ACAGTCATTCCGGCA | 138151 |
| rs548156752 | snp | A/G | 0.00029144 | 0.0120679 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011514 | CAGCCACCCAGCTCC[A/G]CTTACAAGGTCCCTG | 138151 |
| rs548166081 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136086547 | CCAGCACCCAGCCAC[A/G]GTCCCACCCCGGGCT | 138151 |
| rs548169211 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136081446 | AACTCAGCACTCGGA[C/T]CTGCTCTCTGAGCGC | 138151 |
| rs548208827 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136063750 | TAGCCAGGTGTGGTG[A/G]TGGGCGCCTATTATC | 138151 |
| rs548230075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136085938 | GGGGCTGGCAGAGCC[C/T]GGAGGCTGGGCACTG | 138151 |
| rs548252111 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011137 | GCCACAGACCACCGC[C/T]GGCCCCTGCTTCGTC | 138151 |
| rs548328781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136018426 | CCCACATCCTGAATC[C/T]ACAGCGGGCGCCCCA | 138151 |
| rs548366835 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013416 | CCTTGGCTGGTCTGC[A/G]TGTGTCCCAGTGGCA | 138151 |
| rs548403409 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136057674 | CCCAGGGCTGCAGTA[C/G]GGTCTCCCCTGCACC | 138151 |
| rs548410880 | snp | A/C | 0.00279385 | 0.0372709 | intron-variant | NACC2 | GRCh38.p7 | 9:136042661 | ACACACACACACAGA[A/C]ACACACACAGACACA | 138151 |
| rs548444211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136078103 | ATCACGAGGTTTGCC[A/G]TACTATCTTTAAACA | 138151 |
| rs548528109 | snp | C/T | 1.70206e-05 | 0.00291719 | synonymous-codon, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013908 | CAGCAAGACCTTATG[C/T]TTCACCCCTGCACAC | 138151 |
| rs548555091 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009770 | GGAGGCGGCCTCCGC[C/T]TGATGGGTTGTGGAG | 138151 |
| rs548585694 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136019220 | CTGGGCTTTAACGGA[A/G]AACCCGCAGAGAGAC | 138151 |
| rs548611835 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096667 | TGCCACTTCCAAACC[C/G]GCCCCGCAGTCTACT | 138151 |
| rs548704307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136088897 | GGGGGAAGGTTTCCC[A/G]GAGGAGACAGCAGGC | 138151 |
| rs548726778 | snp | A/G/T | 0.00199481 | 0.0315187 | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006118 | GGTGGGGGAGGGGGA[A/G/T]GGAAAGAAGGAGCCA | 138151 |
| rs548778111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136024803 | CAAAAGACCAACTAC[A/G]ACCCTGAGGGGCTGC | 138151 |
| rs548788308 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136026217 | GTGGTGGTGCGCACC[A/T]GTAATCCCAGCTACT | 138151 |
| rs548788399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136084504 | AGACAAACCTACCTC[A/G]AGGGTCCATCTATCA | 138151 |
| rs548808997 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136072325 | CCACGGTGAGCAGAT[C/T]ACTTGAGGCCAGGAG | 138151 |
| rs548945061 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136085608 | GGAGGGGCCTGGGAG[G/T]CGGCTGCCAGGGGGT | 138151 |
| rs548951828 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011777 | GATGGTGGCGGCGTC[A/G]CCCCGCCGCTCGGCG | 138151 |
| rs549037622 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011347 | TTTACAGTATAATGA[A/G]TGCATTTGTTTCCTT | 138151 |
| rs549101350 | in-del | -/AC | 0.0178098 | 0.0926698 | intron-variant | NACC2 | GRCh38.p7 | 9:136053893 | CCAGGGCTGACACAG[-/AC]AGCAAGGGACAATGT | 138151 |
| rs549118135 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007994 | TGACTCTTCCTGGAG[A/G]AGAAAGGAGGCCAGG | 138151 |
| rs549157602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136022184 | TGGCATCAGGCGCAG[A/G]GCAGGTGCACAGGGA | 138151 |
| rs549174865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136027177 | TTGCAGTGAGCCGAG[A/G]TAGCGCCACTGCCCT | 138151 |
| rs549175465 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136083900 | ACCAAGAACCTGGCT[A/G]GCCCAGGCAGCTCTG | 138151 |
| rs549203683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012824 | GCCCTGGAGATGGAC[C/T]GGGCTCCGCCCCCAC | 138151 |
| rs549204041 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007733 | GTTCTTGGAGTTTTC[A/C]GTTGGTTCATGGGCC | 138151 |
| rs549299005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136076064 | CAAAGAACAGTCATC[A/G]AAAACTTGGAAATAA | 138151 |
| rs549322793 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136094214 | CCCACCAGCACGTGG[A/G]TGAAACACCTCCAAT | 138151 |
| rs549330751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136019091 | TGGCTAAAAACACCC[C/T]GCCCCGAGTGGAAGC | 138151 |
| rs549355807 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136020917 | GTGGCACCAAAACCA[C/T]CCTCCGTCTCAGCCT | 138151 |
| rs549364764 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136071372 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAGATA | 138151 |
| rs549384464 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136082916 | GCATGGCCCTCTCTA[C/T]GCCTAGGATTTTGTG | 138151 |
| rs549425149 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136057105 | AGCAGCAGGCTCTGC[A/G]TCCGATAGGGCCTTG | 138151 |
| rs549429705 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136093863 | GACCTAACTCTAGGC[C/G]CCCCTGCTGGGGGGT | 138151 |
| rs549433752 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136017522 | GTTGCCCCCCACCCC[C/T]ACCACCCTGAGTCCC | 138151 |
| rs549450179 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136061948 | ACCATGGCGAAATCC[C/T]ATCCCTACTAAAAAT | 138151 |
| rs549492371 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136067190 | ACCCGGGAGGCGGAC[A/G]TTGCGGTGAGCCAAG | 138151 |
| rs549494219 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136060592 | GTTCAGTCCCTGGCC[C/T]GAGAAGGCCAAGCCC | 138151 |
| rs549502768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136071909 | CGTCCAGACGCAAAT[A/G]TGCTGAACTCCACCC | 138151 |
| rs549551522 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136094612 | ACCCCAGTTTCTCCC[A/C]AGGCTGGGGCCCGAG | 138151 |
| rs549571159 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136063160 | TCTCCTGTCAAACGT[A/G]TGGTTTGAGCCGCAT | 138151 |
| rs549590043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136019570 | GGAACAGCTCATAAA[A/G]AGCAATGAGCTAACT | 138151 |
| rs549602329 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | NACC2 | GRCh38.p7 | 9:136063897 | TCAAAAAAAAAAAAA[A/C]CAAAAAAAACAAAAA | 138151 |
| rs549606150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014854 | GGAAACTTGACCACA[C/T]CCCAGGTGTCCCACC | 138151 |
| rs549612580 | in-del | -/GTGT | 0.00358779 | 0.0422022 | intron-variant | NACC2 | GRCh38.p7 | 9:136024486 | GTGCGTGTGAGGACA[-/GTGT]GTGTGAGGACAGAAT | 138151 |
| rs549630553 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078983 | GCGCCGCCGCCGCCC[C/T]TCTCCGATTCCCTAA | 138151 |
| rs549663157 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NACC2 | GRCh38.p7 | 9:136046582 | GGGGACCGAGACGGG[A/G]CCTGCCTCGCTGCGG | 138151 |
| rs549687349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136090572 | GCACCCAGCTCCCAA[C/T]GCCCTCCATGAGGGA | 138151 |
| rs549795465 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136024742 | GATATGAGGGAGCAG[A/C]CAATATTAGACTAAC | 138151 |
| rs549798476 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136048823 | TCCCATCAGGGCACA[G/T]GGATATGCGTGGTGG | 138151 |
| rs549798887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136030815 | CTCAGGCACACACCT[C/T]CATGCCTGGCTAACT | 138151 |
| rs549849209 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136077957 | GTACTTCTTTTTAGT[A/G]GAGACGGGGTTTCAC | 138151 |
| rs549886755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136031501 | CGCCACCACACCAGG[C/T]TAATTTTTGTATTTT | 138151 |
| rs549920092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136064312 | GACAAAAGTAAATCC[C/T]AATCCTTAAAAACTA | 138151 |
| rs549927641 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136069780 | CTAAGACACAGCAAT[C/G]CTAAATGTCCATGTA | 138151 |
| rs549942677 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136092092 | CCACACACAGCTCTG[A/G]ACTGGGGCCCAGTGG | 138151 |
| rs549947252 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136074768 | ACTCCCAGAGGGCCC[A/G]TGTCGGTGGTCACAT | 138151 |
| rs549989344 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136079625 | GCAGAAGAGAGGCCA[C/G]AGGCCCCCCAGAGCT | 138151 |
| rs550058433 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136059498 | GCTGGGAAACCCCAC[C/T]CGGGCCGCCTCCTTG | 138151 |
| rs550074936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136075500 | GCCGTCTCCTACATC[A/G]CGGTACAGTTTCTCA | 138151 |
| rs550093775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136021029 | CCACAATGGAAATGA[C/T]TGACGAGCTAGAATT | 138151 |
| rs550192703 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136057083 | GGGAGGACGCTCCAT[C/T]CTCGGCAGCAGCAGG | 138151 |
| rs550209619 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136025855 | AGGAGGCAGAGGTTG[C/T]AGTGAGCTGAGATTG | 138151 |
| rs550218163 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136087985 | TGGGGACTCTGCTGG[C/G]AAGTTCCGGGAGGTG | 138151 |
| rs550280736 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136035274 | AGACCACCTGCACCA[A/C]ACCATCAAAGGAACA | 138151 |
| rs550319225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136072036 | TGAGGTCAGGAGTTT[A/G]AGACCAGCCTGGCCA | 138151 |
| rs550351400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136020543 | CAGCAGAGCCTCGGC[A/G]GGGGTAGGAGGGAGA | 138151 |
| rs550360820 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015402 | ACCCCTCCTGGCCAG[A/G]GCAGCCCAACACTGC | 138151 |
| rs550363249 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136028832 | CCTGCTCCGATTTTG[A/G]AGCAAAGTTGTAGCT | 138151 |
| rs550373056 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136065130 | ACAGGATAAATCTTT[C/G]TGGTCTTGGGTTAAA | 138151 |
| rs550380488 | snp | C/G | 0.0260105 | 0.111035 | intron-variant | NACC2 | GRCh38.p7 | 9:136076878 | AGCCGGGCGTGGTGG[C/G]GGGCGCCTGTAGTCC | 138151 |
| rs550555105 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136090804 | GGGCCGGGCTGCCCT[C/T]GGGGCCCCGGTGGCT | 138151 |
| rs550570835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136084865 | TGGGACTCCACTCAC[A/G]TGCAGTCCCGGAAGC | 138151 |
| rs550588526 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136030954 | GAGTGAACCACCGTG[C/T]CCGGCCAATACATCT | 138151 |
| rs550598993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136090098 | AAAACTCTGTTAAAG[C/T]TGATTTTTTAACAGC | 138151 |
| rs550655797 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008604 | GATTCTAGAATTAGT[C/T]ATCTTGTAAACAAAG | 138151 |
| rs550694946 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136091156 | CCATGGCGGCCTCCT[A/C]TTAAAGGGTAGTGAG | 138151 |
| rs550705816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136094878 | CGGCGGGGAGCGCCC[C/T]GGGACGCCCGGAGCC | 138151 |
| rs550735187 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136023578 | CCTGGTCCTGGAGAC[G/T]CAAGAAGTCCCCAAG | 138151 |
| rs550740385 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136058393 | GATTCCCATCCTCAG[A/G]GGTGTCCGGCGGAAG | 138151 |
| rs550760564 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136017676 | GCACTCCTCACACCC[A/C]AGCCTGGTAGGCTGC | 138151 |
| rs550798619 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136029148 | TGGAGTGAGAACTTA[C/T]GTTGCCTTTTCCGGG | 138151 |
| rs550948387 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136095750 | CCTGCCCGCGGCAGT[C/T]GCGTCCGCACGGTGC | 138151 |
| rs550949921 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013754 | CTGAAGTCAGGAATG[C/T]GAGAGGGCTTTCAAT | 138151 |
| rs551059406 | in-del | -/AAAC | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136065640 | CATAAATAAGTAAAT[-/AAAC]AAATAATAAAAAATT | 138151 |
| rs551061039 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136016834 | ACGGCGCAAGACAGG[A/G]TGGAGGATGGAGGAC | 138151 |
| rs551151873 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136088841 | CCACAAAGGGACCTA[A/C]CCCAAGCCCCGAGGG | 138151 |
| rs551232627 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136042449 | TGCAGGTACGTATTC[A/G]ACTGATTCTTGTCAA | 138151 |
| rs551301060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136082563 | CTGGCCCTCGGAGCC[C/T]GACAAACAAAACCAG | 138151 |
| rs551319120 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006459 | GGGGACCATTGGCCA[C/T]CCCTGCCTTCAATAG | 138151 |
| rs551320272 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136043277 | TAAAATCTAATTTTT[A/T]AAAAATGGACAAAAG | 138151 |
| rs551329424 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136088677 | CCAGGAGGCATCGTG[G/T]TCTGGGGTCACTGAG | 138151 |
| rs551331530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136065265 | TGAGGCAGGAGTATC[A/G]CTTGAGCCCAGGAGT | 138151 |
| rs551342561 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136083977 | CACCCCAACTTCTCC[C/T]GCATCACTGGGTGGG | 138151 |
| rs551382929 | snp | C/T | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096580 | CAGGGACTCTGGGCT[C/T]TCCCCACAGAGTCCC | 138151 |
| rs551388878 | in-del | -/AGTT | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136055835 | TGGAGACTGCCTGGC[-/AGTT]AGTTAAGTGAGGACA | 138151 |
| rs551408560 | in-del | -/CACACATA | 0.0607341 | 0.163335 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007424 | ACACAGACGCGCGTG[-/CACACATA]CACACAGACGCGCAC | 138151 |
| rs551427540 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136063632 | CTCACGCCTGTAATC[C/T]CAGCACTTGGGAGGC | 138151 |
| rs551442310 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016540 | TTAGACCCACTCTGC[C/T]CACCTGGGCCCAGGT | 138151 |
| rs551499904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136060789 | CCCCACCAGCCTGCC[A/G]GTCTCCAGGCTTCAG | 138151 |
| rs551513910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136060361 | GGGCTGCCTTTAAGC[C/T]GGGGCCATAAAAGGT | 138151 |
| rs551529346 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136027169 | GGCGGAGGTTGCAGT[A/G]AGCCGAGATAGCGCC | 138151 |
| rs551610830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136026682 | GGTGCTTACAACATA[C/T]ACAGAATTAACACAC | 138151 |
| rs551627203 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136085800 | CATCTGAAGCAAAGT[C/T]CCCACCTGCCAATGC | 138151 |
| rs551634702 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136055235 | ACTGCAGCCAGACGC[A/G]CACACAGGGGTTGGG | 138151 |
| rs551637935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012316 | GTTTTTAATCTCTCC[A/G]GGCTTCCGTAGCCCC | 138151 |
| rs551653849 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136066887 | ATGCTGGTCACAAGA[C/G]GGCACATATTATGAG | 138151 |
| rs551673893 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136031986 | GGTGCTCTGCATAAA[C/T]GAATGGGGGGCAAGG | 138151 |
| rs551684220 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136079753 | CTCCCACTACCCATT[C/T]TGCGACTAGGAATAG | 138151 |
| rs551720574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136055803 | AGAGTCCCTCTACCC[C/T]GAGCCCCGGCCCCTG | 138151 |
| rs551741355 | in-del | -/CTC | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013045 | GAGAGCTGCTCTTTT[-/CTC]CTCATCTTCCCCTCA | 138151 |
| rs551793786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136061895 | GAGGCCAAGGCGGGC[A/G]GATCACCTGAGGTCA | 138151 |
| rs551803926 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007694 | CTGCGCTTAGGACTC[A/G]CTGCTGGCAGAGGCA | 138151 |
| rs551804875 | in-del | -/GTGTGAGGACAGTGT | 0.0263992 | 0.111815 | intron-variant | NACC2 | GRCh38.p7 | 9:136024475 | GAGGACAGAGGGTGC[-/GTGTGAGGACAGTGT]GTGTGAGGACAGAAT | 138151 |
| rs551823253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136024596 | AGGACAGAGTGTGCA[C/T]GTGAGGACCAGCAGG | 138151 |
| rs551888615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136071351 | AGTTTGAGACCAGCC[C/T]GGCCAACATGGTGAA | 138151 |
| rs551907381 | snp | C/T | | | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014181 | CAGCAGGTCCCAAAT[C/T]ACACATGGAACTAAG | 138151 |
| rs551998445 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136019059 | CTATTTCTGCCTTGC[C/T]GTGCACCGGGTGCTG | 138151 |
| rs552001007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136093781 | GAGGGGTGCTCCAAC[A/G]GTGGCCGGGAGAAGA | 138151 |
| rs552047799 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136058882 | AGGGGACGCAGGGGC[C/T]GGGGCAGGATGGTCT | 138151 |
| rs552051072 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136062351 | TGGAAAGTTACAGGT[A/G]TACATGTCAGCTTTT | 138151 |
| rs552068691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136094149 | ACACACAGGAAGGAA[C/T]GCGCAGCAGAGAACA | 138151 |
| rs552136062 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136089452 | CTCAAGGCCCTTCAG[C/G]TTCTGCTCTGCCTGA | 138151 |
| rs552186216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136059373 | ACATGCCAGCTCAGC[A/G]CCTCCAGAGAGAAGC | 138151 |
| rs552189185 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007843 | GTGGGGTGGGGGGAC[C/T]GGGCCAGCGCTTAAC | 138151 |
| rs552189240 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136063790 | CAGGAGGCTGAGGTA[C/G]GAGAATCACTTGAAC | 138151 |
| rs552192741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136029876 | CCCTCAGAGGTGTGG[A/G]ATCCGGGCCGGTAGT | 138151 |
| rs552273925 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136046431 | GAGGCTGCCGGCCAC[A/G]GGGCCAGGAGGAAGG | 138151 |
| rs552291979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136087020 | ATATCCCGGATTTAG[A/G]GTGGACCCTAACATG | 138151 |
| rs552306544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136079104 | AGTTTAGGGCACGTA[A/G]CCTGAAATCTACTCA | 138151 |
| rs552307743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014239 | CCCACCCTCCCCAAC[A/G]AGCCCCAAACTCCAA | 138151 |
| rs552315895 | in-del | -/AAAT | 0.0260105 | 0.111035 | intron-variant | NACC2 | GRCh38.p7 | 9:136072851 | GTGAAACTCCGTCTC[-/AAAT]AAATAAATAAATAAA | 138151 |
| rs552321726 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136068152 | CTATATGCTACTAAA[A/G]ACTGTATAAACACCG | 138151 |
| rs552378755 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136073488 | GGAGCTGCAGTGGAC[-/A]GGGGGTGTGAGCGTG | 138151 |
| rs552464852 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009829 | CACCGCTCACTGGCC[G/T]GTGTGCACACCGGAG | 138151 |
| rs552476254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136025722 | AGTTCGAGACAGCCT[A/G]GCCAAAACGGCAAGA | 138151 |
| rs552499320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136075149 | CAGGCCAGGAAGTGG[A/G]GAGCCCCAGGTGTGG | 138151 |
| rs552536372 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136017435 | CCCAGCATGCACCAG[C/G]TGCGCGGGGCCAAGG | 138151 |
| rs552536583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136087549 | GCTGGGGAAGGGCCC[C/T]GCAGCTTCTGGGGCC | 138151 |
| rs552540339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136031429 | TGCAAACTCTGCCTC[C/T]CGGGTTCGAGCAATT | 138151 |
| rs552540569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136079896 | TGCTGTGGAAGGAGC[C/T]GCTAGCCCTGCCACC | 138151 |
| rs552677632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136080332 | GATGCCACCTCTCAG[A/G]GCATCCAAAACCCAA | 138151 |
| rs552772666 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136019723 | CCTCCCTGGACCACA[C/T]GGGGCGAAGCAAACA | 138151 |
| rs552803592 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136093616 | CCAAGTGGCTTTGCC[G/T]AAAGGACAGGGGGCC | 138151 |
| rs552820827 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NACC2 | GRCh38.p7 | 9:136069736 | AGAGATAGAGTAGGA[C/T]GTGACATAATAATTA | 138151 |
| rs552848231 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136025223 | GAATGTGGGCACGGG[C/T]GCTGCTGGATGGCAC | 138151 |
| rs552862180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136016627 | CCATCCCTACTTGGT[A/G]CCCTCTTGCCCACCT | 138151 |
| rs552906506 | snp | C/T | 0.00636936 | 0.0560724 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007783 | CTGCCAAGATGTTTC[C/T]ATAAAAATTTCCCTT | 138151 |
| rs552910783 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136038146 | GGAGTCAGGGGAAGC[-/G]GGGGGGAAATGACCA | 138151 |
| rs552919540 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136068448 | AGGTTGCAGTGAGCC[A/G]AGATCACACCATTGC | 138151 |
| rs552935804 | in-del | -/ATC | | | intron-variant | NACC2 | GRCh38.p7 | 9:136068059 | CTCTATAGGACACTT[-/ATC]ATGAATGGAACTTGC | 138151 |
| rs552943437 | snp | A/G | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012967 | TATTAAAATAGTTTC[A/G]CAGCTGAATTCATCA | 138151 |
| rs552957475 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010626 | AAAGTTTCCAAACCA[C/T]ATATGAAATAGATCT | 138151 |
| rs552992277 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136093928 | TGAGTGTCCCACTGG[A/G]GAACAGGAGGGAAGG | 138151 |
| rs552996367 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007548 | GTGCACACACAGACA[C/T]GCACACACACACAGA | 138151 |
| rs553060692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136021410 | GGGACGTCCTGACGA[C/T]GTGGTCTCACCTCCC | 138151 |
| rs553099407 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136035811 | ACATGTAAAAAGAAT[C/G]ACAGAGCAGATGTGG | 138151 |
| rs553116838 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136073059 | ACAGGTAATGGGATG[A/G]AAAGACAAGACACAG | 138151 |
| rs553136429 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008798 | GTCCACAGACACTCC[C/T]GACTCACGCCCACCG | 138151 |
| rs553187321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136033381 | GGGCACGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 138151 |
| rs553238701 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | NACC2 | GRCh38.p7 | 9:136017904 | CCTGCCCGATTGCAC[C/G]AGGGCAGCCTGCAGG | 138151 |
| rs553246870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136021754 | GAACCATCCACATGA[C/T]GTGTTACCGCTTGGC | 138151 |
| rs553261245 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136083416 | ACACTTTGGCCTTCA[A/C]CCCTGTACTAGGAAT | 138151 |
| rs553313530 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009899 | TGAAGATGGGGAAGC[A/C]GAGTTCTGGAGGGAC | 138151 |
| rs553333788 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136075579 | GCATCTTCTTTTATC[C/G]GGCATAGGCCCACAT | 138151 |
| rs553372264 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136089271 | TCTGGCCAGGGCCCA[C/G]GGCCTCAAAGGAGGA | 138151 |
| rs553377019 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136062035 | TGAGGCAGGAGAATC[A/G]CTTGAACTGGGGAGG | 138151 |
| rs553378335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012342 | GCCCCAACGGCTAAC[A/G]GGAACTGGTCAGAGG | 138151 |
| rs553398810 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136090251 | TGGCCAGAGGGGATG[A/C]CTCAGGGGTCCCTGG | 138151 |
| rs553399380 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009528 | ATGGTCCCCCACCTC[A/C]TTCTGGAAAGCAACG | 138151 |
| rs553452387 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136091081 | GCCAGCCTCTCCTCC[C/T]TGTGGGTCCCTGCAA | 138151 |
| rs553501617 | snp | A/G/T | 0.00358891 | 0.0422285 | intron-variant | NACC2 | GRCh38.p7 | 9:136057152 | TTGGCTCTGCCGGGG[A/G/T]TCTGGTCCAGGGGCC | 138151 |
| rs553512053 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136056636 | GCAAAGGCCCCCAGC[C/T]TCAGGGTCACAGAGG | 138151 |
| rs553535636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136085568 | GTACTGAGGGGTCTG[C/T]ACTGGATCTGCTGGT | 138151 |
| rs553581224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136030391 | AAGGCAGGCAGATCA[C/T]GAGGTCAGGAGATCG | 138151 |
| rs553608242 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136080825 | GACGGCAGATGACCA[A/C/T]AGGCCGGCCTGTGCC | 138151 |
| rs553649464 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136028942 | GCCCCCTCTGGATGT[C/T]GGGCACCGTCGAGCA | 138151 |
| rs553667623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136024933 | AGGATCCTGAGAGCC[A/G]GCCTCAGGGTGCAAT | 138151 |
| rs553704571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136091723 | TAGGGCTCCCAGCAA[A/G]TGGGCAGCTGCAGGT | 138151 |
| rs553714175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136046609 | GCGGGTGGGGGGGCT[C/T]GAACTCGGCCCCATC | 138151 |
| rs553737754 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136076980 | CACTGCACTCCAGCC[C/T]GGGCGACAGAGCGAG | 138151 |
| rs553754801 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136057776 | CTCGCTCACCCCCTC[C/T]CTTGATGGCCTGGAG | 138151 |
| rs553794867 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136087219 | CTGGAGGAACCAGCC[C/G]TGAAGATGCACAGAG | 138151 |
| rs553821490 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136045225 | GCACACAGGGGACAC[A/C]GGGTGGACCCCAGAG | 138151 |
| rs553895948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136064755 | GCAAGGGACCCAGGA[A/G]AGCCAAAACAATATT | 138151 |
| rs553997572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136083268 | GTCCAGGTACAGTCA[A/G]TGCTTCACCCCAACC | 138151 |
| rs554010570 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136083644 | CGGGCATGAGCCCAG[C/G]GCACCACAGGCGGCT | 138151 |
| rs554080667 | in-del | -/T | | | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016152 | AGAGGAAATTTAAGA[-/T]TTTTTTTTTTGACTG | 138151 |
| rs554104284 | in-del | -/A | 0.497241 | 0.037038 | intron-variant | NACC2 | GRCh38.p7 | 9:136067268 | GGGAAACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 138151 |
| rs554145554 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136020058 | TGGGGAAGATGGGAA[C/G]TTCTGGAGCCGATGG | 138151 |
| rs554161034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136055542 | ACCCTGCCCCCTCCA[C/T]CCCTAGATTGTAAAG | 138151 |
| rs554162050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136074912 | GCCGGGGGATGCTGG[C/T]GGGAATGGGTTCTCG | 138151 |
| rs554178932 | in-del | -/CCC | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136023932 | ATACACACGTGCATG[-/CCC]CCAACCACACAAATG | 138151 |
| rs554218361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136071654 | TAGCTAAGACAATTT[C/T]GAGAGAGAATTAAGT | 138151 |
| rs554233290 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136073670 | AAGTCGACTTGATTT[-/C]CCCTCGGTTCATAAT | 138151 |
| rs554281743 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136076649 | TGTTCTTACTGCCAC[C/T]GAACTGTGCGCTTAA | 138151 |
| rs554284412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067115 | CAAAATTAGCCAGGC[A/G]TGGTGGTTCATGCCT | 138151 |
| rs554363136 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006125 | GAGGGGGAGGGAAAG[A/G]AGGAGCCACGCACCT | 138151 |
| rs554448922 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078049 | AGTGCTGGGATTATA[A/G]GCATGAGCCACCGCG | 138151 |
| rs554450978 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011061 | GAGCCCTGCCCCGTC[A/G]CCCCAGAGAGGTTCC | 138151 |
| rs554456491 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136050995 | AGTTCCAGCCCGCAC[A/T]GGAGCTCCCGGGAGG | 138151 |
| rs554461272 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136077022 | AAAATAAATAAATAA[A/G]TAAATAAAATAGCCG | 138151 |
| rs554501267 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136076912 | CTACTTGGGACTAGG[C/T]GGAGAATGGCGTGAA | 138151 |
| rs554522533 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136093417 | TAAAGAACAGAGCCT[A/G]TTCTCGCAGCCTGTA | 138151 |
| rs554530348 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136006649 | GTCTGAAACGGCTCT[C/G]AGCACGCTTGAAGCC | 138151 |
| rs554531351 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136081708 | GGCCAGGAACACACA[C/G]AGCCCCTCCTGGCTC | 138151 |
| rs554561622 | snp | A/G | 0.030278 | 0.119257 | intron-variant | NACC2 | GRCh38.p7 | 9:136035742 | GTTCAGCCTTTTGAT[A/G]TAAAGGGCATAATAT | 138151 |
| rs554572105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136057191 | TGAGCCGAGCCCTGC[A/G]CTTATGGGGAATGAC | 138151 |
| rs554572123 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015844 | CTGAGCGAGGCCCGG[-/C]CCCCACGGGCTTCTG | 138151 |
| rs554599313 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136087398 | CCTCCTGGCCTGTCA[C/G]CTGCACAGCTGCAAA | 138151 |
| rs554680612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136082212 | CTGCCCGTCTCCCCA[A/G]GGTCTTCACCCTCAG | 138151 |
| rs554689455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136072067 | ACATGGTGAAACCCC[A/G]TCTGTACTAGAAATA | 138151 |
| rs554690383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012499 | GTCATTCCTCCCAAC[A/G]GCATCAAACCCAGAG | 138151 |
| rs554783011 | in-del | -/CA | 0.473966 | 0.111081 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007468 | GCGCACACAGACGCA[-/CA]CACACAGACGCACAC | 138151 |
| rs554793108 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096346 | GGGCTACAGCCCTTC[G/T]GGCACAGTCAGCCAA | 138151 |
| rs554801031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015794 | ATCTACAAGGAGCTA[C/T]GACGCCAAAGGAATC | 138151 |
| rs554815042 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136055532 | GTCCCCAGAAACCCT[A/G]CCCCCTCCACCCCTA | 138151 |
| rs554840927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136057689 | GGGTCTCCCCTGCAC[C/T]GGCTCGGCCGGGTGG | 138151 |
| rs554853979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013096 | CCCAGGGACGGAAGC[C/T]GCAGGTGGCCGGGAG | 138151 |
| rs554873905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136018157 | CCGCACCAGGACGCT[C/G]AGAGGCAGGTGCACC | 138151 |
| rs554876513 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NACC2 | GRCh38.p7 | 9:136038342 | GGCGTTCCAGACCAG[C/G]CTGGGCAACGTGCTG | 138151 |
| rs554926445 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008764 | GAGCACACAGCAGGT[C/T]CGCTCAGCAGCCACG | 138151 |
| rs554940505 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136022908 | TACCACGCCATGCCA[C/T]GCCACACCGTGCCTG | 138151 |
| rs554954749 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136088164 | GCAGCCCCTTGGCTG[C/T]GCAGGGTCAGCGGAA | 138151 |
| rs554978486 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136038218 | ATCTTGACTGGGGAG[G/T]TGACTACATGACTAT | 138151 |
| rs555039435 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078651 | GCCCAGCCCCGACAT[C/T]GGGACAGAAAGGGGC | 138151 |
| rs555052710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136029972 | GGGTAAAGGCACCAC[C/T]GGCCACAGAGGTTTC | 138151 |
| rs555097076 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136073650 | CAACCCAAGAATGTT[G/T]GCAGAAAGTCGACTT | 138151 |
| rs555108877 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006037 | GAAGGCCAACCCCGC[A/G]GGCCCAGCTCTGCCC | 138151 |
| rs555117973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136029585 | AGCCCTTCGGGGATC[C/T]CAGACCCAGGAGGTC | 138151 |
| rs555156726 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136077839 | GTGAATAAGGAATCA[C/G]TGATGAATACTGACT | 138151 |
| rs555223621 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136075646 | CCTGCAGGGCCCCCT[C/G]AGGAAACCTGTGCTG | 138151 |
| rs555242684 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136024206 | GTGTGTGTGAGGACA[C/G]AGTGTGTGTGTGTGA | 138151 |
| rs555247810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136021362 | AAACGTAAAAACACC[A/G]ACGCCAAGTGCCGGC | 138151 |
| rs555259149 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008898 | CATTAAATTATTATT[A/G]TTTAAGTTTTATCTA | 138151 |
| rs555305438 | snp | C/T | 0.000218091 | 0.0104402 | missense | NACC2 | GRCh38.p7 | 9:136011893 | TGCGGTACATCTCCA[C/T]GCCCTCCGGCAGCAT | 138151 |
| rs555310789 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136026791 | GGGGAAAATGGAATA[A/C]CTGATTAATCAGAAA | 138151 |
| rs555314958 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136022017 | AAGGTCGGGCTACAC[A/C]CCTGTCCCCACGGGG | 138151 |
| rs555341030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067938 | TATAGAGCATGTTAC[C/T]GTACTGAATAGCATA | 138151 |
| rs555352505 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136062177 | CAGGACAGGACAGGA[A/C]AGGAAAGAGAGAGAA | 138151 |
| rs555369658 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NACC2 | GRCh38.p7 | 9:136020587 | TCCCTAAAAGTGTAT[A/G]CCATTTGTTAAAATG | 138151 |
| rs555391004 | snp | A/G | 0.000152172 | 0.00872141 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011696 | GTCCACCTCCTCGCC[A/G]GCGTCGAAGGCGGGG | 138151 |
| rs555391715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136026168 | AACATGGCAAAACTC[C/T]GTCTCTACTAAAAAT | 138151 |
| rs555395538 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NACC2 | GRCh38.p7 | 9:136020542 | CCAGCAGAGCCTCGG[C/T]GGGGGTAGGAGGGAG | 138151 |
| rs555429032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136049154 | GGAGGGGGAGCGACT[A/G]CTCACTCGGCTCAGC | 138151 |
| rs555437072 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136025922 | ATCTCGAAAACAAAC[-/A]AAAAAAAATCCAACA | 138151 |
| rs555455237 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136032005 | TGGGGGGCAAGGGTC[A/G]TCCTCGGCAGCACCC | 138151 |
| rs555457857 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136016667 | CTCACAGGGAAGCTC[C/T]TGTGAACGAGTGAGC | 138151 |
| rs555514620 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136031704 | TCCTTAAAGCAAAAT[G/T]AGAGGGCAATCTCTC | 138151 |
| rs555556219 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007479 | CGCACACACACAGAC[A/G]CACACACGCACAGAC | 138151 |
| rs555567707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136032473 | GAGCAAACATCCTAC[C/T]TAAAGAGGAACAGTG | 138151 |
| rs555594182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136028502 | TGCCTCAGCCTCCTG[C/T]GTAACTGTGACTACA | 138151 |
| rs555640283 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067195 | GGAGGCGGACGTTGC[A/G]GTGAGCCAAGATCGC | 138151 |
| rs555655611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136027425 | TTCCTTATCAGCACC[A/G]TTTATGCTATTTCTT | 138151 |
| rs555677558 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136066051 | ATACAAAACTAGCCG[G/T]GTGTGGTGGTGGGTG | 138151 |
| rs555696083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136061173 | CTGCACAGCCCCCAC[C/T]GTGAGCTCAGACTGT | 138151 |
| rs555705394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014032 | GGGTCCGAAGAGGCG[C/T]ACAGATGGGTGAGGG | 138151 |
| rs555715758 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136060311 | GGGAGGCCTGCACTT[G/T]GCTTTGGGATCACGG | 138151 |
| rs555738614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136070432 | GAACTACTTGAACCC[A/G]GGAAGCGGAGGTTGC | 138151 |
| rs555742126 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136018634 | GGCTGCAACAGAACA[C/G]AGGCCAGAAAGGGGG | 138151 |
| rs555771860 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136093265 | TCAGCACCAAGATCG[G/T]CACTGTTGTTTCATG | 138151 |
| rs555778910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136057893 | GAGGCGGTCTGGAGC[A/G]TGCTGGGCCCCGCTG | 138151 |
| rs555780705 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136076683 | ATGGTTAAAATGGTG[A/C]ATTTCATGTTGTGTA | 138151 |
| rs555781713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016575 | CCACTCTGTGCCGCT[C/T]TCCTGCTGGCCTGGG | 138151 |
| rs555849416 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008952 | AACAAAACAGACGGC[A/G]ATTACAAACGAGTGA | 138151 |
| rs555853360 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136063157 | CTCTCTCCTGTCAAA[C/T]GTGTGGTTTGAGCCG | 138151 |
| rs555927686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136080438 | TTAGCTGGGCGTGGT[A/G]GCGCACGCCTGCAAT | 138151 |
| rs555935059 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136095453 | GGGGGCCGGGAGGGT[A/C]CCCAGTGGGGGCCGG | 138151 |
| rs555937880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136089530 | AGCCCCTCCCCCAGC[A/G]CTGGGGGCCTCTCCC | 138151 |
| rs555990181 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007041 | TGCACCCAGTGCCAT[C/T]CAAATCTTCAAGTCA | 138151 |
| rs555991480 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136030348 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 138151 |
| rs555998846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136091482 | CCCTGGGTCAGGGTC[C/T]CAAATGCCCTCCCCT | 138151 |
| rs555999268 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136065566 | CAGAGGTTGTGGTGA[C/G]CCAAGATTGCGCCAC | 138151 |
| rs556020609 | in-del | -/CGCG | 0.0023933 | 0.0345097 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136095382 | GGACAGCGCGCCGGC[-/CGCG]CGCGCGCGCGCACTG | 138151 |
| rs556054170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136043750 | GGGAACTGTTCTGTA[C/T]GTTGATTGCAACATT | 138151 |
| rs556113144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136059028 | GCAGTGTGGGGGCTG[C/T]AGAGGGAAGGTGCTG | 138151 |
| rs556132810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136080757 | TGGAGACGGGGGGCC[A/G]TGACACACACCCAGA | 138151 |
| rs556147673 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136020335 | CAGGCAAAACACCCC[A/G]AGATCCCTGCCCACG | 138151 |
| rs556171166 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136056025 | CGCAACGCCTTCCCT[A/T]TCCCATACGGTGCAG | 138151 |
| rs556214041 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136058315 | ATCCCTGCCCCACCC[C/T]ATCCTGCCCGGTCCC | 138151 |
| rs556228516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136063402 | AGGAAAGAGGTCACG[C/T]ACATTGCAGAAGCAA | 138151 |
| rs556281175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136074868 | GCGGCAGGAAGCGTG[A/G]CCTTCCCAGCCGAGG | 138151 |
| rs556370666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136019835 | CTGCTCCCAGCCGGG[C/T]GACACCAGGGGAGCT | 138151 |
| rs556403797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136086668 | TGTTCCCAAACTTAC[A/G]TAACCGCAGATGACA | 138151 |
| rs556407383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136025277 | TCACGCAACAGTCCC[C/T]AGACCCTTTGAGGAG | 138151 |
| rs556456131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136082759 | CAGCCCCCTCTCCCC[A/G]GCGGGTGGGGCTGGC | 138151 |
| rs556537553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136078302 | CGCCAGAATTCCACG[A/G]AGCTCAGTCCCTCGG | 138151 |
| rs556553308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136092784 | TCTCCGGAGAAACAT[A/G]CTGGTGTATCCTGGG | 138151 |
| rs556584394 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136065312 | CAACATAGTGGGACC[G/T]CGTATCTACAAAAAA | 138151 |
| rs556618742 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136071514 | TGCCAATGCACTCCA[A/G]CCTGGATGATAGAGT | 138151 |
| rs556643944 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136019308 | GAGGCCCCGTGAGTC[A/G]GGGCCAGAGCTGGGT | 138151 |
| rs556682088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136076569 | TGGTGTTCAATGGGT[A/G]CAGTTTCGGTCAGGG | 138151 |
| rs556683387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014540 | GCAATCTTCCCACTT[C/T]GGCCTCCCAAAGTGC | 138151 |
| rs556703337 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136092379 | CCAGTGAGACCAGAC[A/C]CAGTCAGACCTCACA | 138151 |
| rs556716612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136027320 | GATAGAAAGAGATGT[A/G]CCAGGTAAATATTAA | 138151 |
| rs556760813 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010699 | CAAAGTGGCTGAGGC[A/G]GCAGAGGGCAGCGTG | 138151 |
| rs556771229 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136025265 | CACTGCAGACCTTCA[C/T]GCAACAGTCCCCAGA | 138151 |
| rs556807147 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136089731 | TTCCCTCTTCATTTA[A/G]GAGCCACGGCCGACC | 138151 |
| rs556817614 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136059891 | TCCACCCTAACTCAA[A/T]TGCAGCCAAGACCCA | 138151 |
| rs556845284 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136067061 | TTCGAGACCAGCCTC[A/G]GCAAGCAACATGTCG | 138151 |
| rs556865626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136093973 | CCAGACGAAAAGAGG[A/G]GTGGGTGAGAAGAAG | 138151 |
| rs556872770 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136080747 | TCCAGACACGTGGAG[A/G]CGGGGGGCCGTGACA | 138151 |
| rs556873542 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011008 | CTGGCCCCGAGTCTC[C/T]GAAAGAAGGAAAAAC | 138151 |
| rs556883687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136047042 | GCCTCTCACTCAACA[A/G]GTAGGGAGACTGAGG | 138151 |
| rs556918619 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136075903 | CCTACAAAGCGCCCA[G/T]GAGCAGCCCCGCAGC | 138151 |
| rs556943928 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136090328 | AGGGCCAACGCTGAC[C/T]CCCTCCAAGACCGCC | 138151 |
| rs557042917 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136028311 | TGGGAGGGCCAGAGA[A/G]TAAATACTTTAGGTA | 138151 |
| rs557057030 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136027098 | GGTGTGGTGGCACAT[A/G]CCTGTAGTCCCAACT | 138151 |
| rs557057276 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009419 | TGCACCACTGAGCCA[C/T]CTGCAGCCCTAGGAA | 138151 |
| rs557066812 | snp | C/G/T | 0.00239401 | 0.0345304 | intron-variant | NACC2 | GRCh38.p7 | 9:136086058 | GGAGTCCGGGCGCCA[C/G/T]GCAGGGCAGCTCCGA | 138151 |
| rs557195883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136017288 | CCTCGGAGGCTCCTG[A/G]GCCACACAGCCCATG | 138151 |
| rs557205119 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136062650 | CTGGGCACAGTGGCT[A/C]ATGCCTGTAATCCCA | 138151 |
| rs557220109 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | NACC2 | GRCh38.p7 | 9:136018089 | GGGGTGGAACCTGCA[A/C]GTCCAGCAGGCTCGG | 138151 |
| rs557268365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067322 | GAGCAGTGGGGGTGG[A/G]GGAGGGATGGGGAAA | 138151 |
| rs557271675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013015 | AGAACGTTAACACCT[C/T]GAGACCTGGCTTCTG | 138151 |
| rs557277780 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136056687 | ACGGGCCCCCTCGGA[C/G]TATCACTGTCGCCCC | 138151 |
| rs557340449 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136092283 | CTGCAGACACTCACC[A/G/T]CCGGGGAGCCTGACC | 138151 |
| rs557356845 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136070910 | CAGACCCTGCAGATA[G/T]CAAAAGGATAACGTG | 138151 |
| rs557483320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136077255 | AGAATTGCTTGAACC[C/T]GGAGGTGGAGGTTGC | 138151 |
| rs557500798 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | NACC2 | GRCh38.p7 | 9:136070776 | ACAGAGGAGGAAAAA[A/C]ATCAATGAAACAGCT | 138151 |
| rs557501798 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NACC2 | GRCh38.p7 | 9:136035629 | GGTACAGTCTGTAGT[C/T]ACATGAGGATGATGG | 138151 |
| rs557510936 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010557 | ACCCCAAGCCATGGT[G/T]GGCTGGGGACAGGGA | 138151 |
| rs557552102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136081566 | GTAATCACAGCTGCC[A/G]AATCTCTGCAAAGGC | 138151 |
| rs557557939 | in-del | -/AC | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136035835 | ATGTGGTAAATTCCT[-/AC]ACCAATTGTGAAGGG | 138151 |
| rs557570218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136029468 | AGAACTCGGGACCTG[C/T]CAAATGGCAGGATTA | 138151 |
| rs557597141 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010433 | GAGCTCAGCTTCACA[C/T]GTACTAGTCGCCCAC | 138151 |
| rs557658517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136023792 | CCACCTATCACAGCA[C/T]ATGGCACGGGTCACT | 138151 |
| rs557668959 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136073465 | AATAAAAAATGAGGA[A/C]CCCAGTAGGAGCTGC | 138151 |
| rs557672374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136083593 | GGACACCTGTGAAGA[A/G]CGCCGTGCAGAGGCC | 138151 |
| rs557728164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136072821 | TGCCATTGCACTCCA[A/G]CCTGGGCAACAAGAG | 138151 |
| rs557731169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136087796 | GAGGACAGCCCAGGA[C/T]GGCACCGGCAAGATC | 138151 |
| rs557734921 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015625 | ACTGCTCAGGCTGTG[A/G]CCAAGGAAAGCGCCT | 138151 |
| rs557761081 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136059853 | CAGAGTCCCTACCTC[A/G]CCGTCAAAAGGACCC | 138151 |
| rs557775881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136021325 | AATCAAGCCATGTTG[C/T]GGTCCCACCTCCCAG | 138151 |
| rs557829496 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136032487 | CTTAAAGAGGAACAG[C/T]GGAAGCTTTTCCTGA | 138151 |
| rs557847325 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136080454 | GCGCACGCCTGCAAT[A/C]CCAGCTACTCGGGAG | 138151 |
| rs557848194 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136028025 | AGCACTTTGGGAGGC[C/G]AAGGTGGGTGGATCA | 138151 |
| rs557881670 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136049135 | TGAAAGAAAGGAACG[C/G]AGAGGAGGGGGAGCG | 138151 |
| rs557898057 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136046824 | CCCTTGCCGTGAGGC[C/G]ACACAGACCATGGGG | 138151 |
| rs557904477 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136055626 | AGGATCACCACCAGC[A/G]AGGGGAAGGGAGGCG | 138151 |
| rs557949538 | snp | A/G | 0.000798403 | 0.0199641 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011582 | CGTCTGGGGCCTGCT[A/G]GGGCCGCCCCCGCCC | 138151 |
| rs557967072 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136025463 | AACAAAACAACAAAA[A/C]AAAACCAACAATTTA | 138151 |
| rs558029714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136032422 | GAAATGAAATAAATT[C/T]CCTTAATCTGATAAA | 138151 |
| rs558041873 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136056052 | GCAGGCTCCAGGAGG[A/G]TTTGCTTTGACCCTA | 138151 |
| rs558059183 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009974 | TCTGGCCACACCTGG[A/G]AAGGAGGGCTGCCCC | 138151 |
| rs558100445 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011134 | CTCGCCACAGACCAC[A/C]GCCGGCCCCTGCTTC | 138151 |
| rs558111892 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136006776 | CAGCACAAAAACAGA[A/G]TGAGGGCTCAGGAAA | 138151 |
| rs558115278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136075335 | CTTGGGGGGAAAGCC[C/T]TCCCTAGCTCCCCCG | 138151 |
| rs558135969 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136017736 | GGAGCACCGCCTCCC[C/T]CATTCCTGTGTCCCA | 138151 |
| rs558139892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136070273 | AGCATTTTGGGAGGC[C/T]GGGGCGGGTGGATCA | 138151 |
| rs558151634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136069962 | CAGGATCTAACTGAC[A/G]TTACAGAACTCTCCA | 138151 |
| rs558163152 | in-del | -/AA | 0.046621 | 0.146521 | intron-variant | NACC2 | GRCh38.p7 | 9:136033648 | GCAAGACTCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 138151 |
| rs558174715 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136023759 | CTTGTCCAGCCATAG[G/T]CACAGGTTGAATCAA | 138151 |
| rs558224616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067441 | GACGTGTTGATTAAC[A/G]ACGGGGATATATCCT | 138151 |
| rs558234827 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013131 | CCCGCGGCCCACCCA[C/G]TCCTCCTCAGGCTGG | 138151 |
| rs558284450 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007445 | TACACACAGACGCGC[A/G]CACACACGCGCACAC | 138151 |
| rs558289781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136072163 | GAATTACTTGAAACC[A/G]GGAGGCGGAGGTTGC | 138151 |
| rs558299754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136057738 | CCCAGGCGGAGCGGC[C/T]GGGAGGGGAAGCACC | 138151 |
| rs558300726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136061598 | CGGGGGTTGAGACCC[C/T]GTGCGGCTCACACCT | 138151 |
| rs558303847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136063389 | TGTTCTTCAATCCAG[A/G]AAAGAGGTCACGTAC | 138151 |
| rs558327136 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136084153 | AGCCAGGAGGGGACC[A/C]GTCTTTCCAGGAGCA | 138151 |
| rs558380315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136089065 | AAAAACACACAGACA[C/T]GAAATCTGTCTGTTG | 138151 |
| rs558392454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136093472 | GCAGGAGATCTCCCG[A/G]GTGGCTCCTCCCCGC | 138151 |
| rs558426383 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009417 | TCTGCACCACTGAGC[C/T]ACCTGCAGCCCTAGG | 138151 |
| rs558435696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136058161 | CCCTGGCTGGCAAGG[A/G]GGCTGCTGGCACCAC | 138151 |
| rs558437930 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136032090 | ACTCCTGGGATCCCA[C/G]CGGCCTTTTCTGTCT | 138151 |
| rs558453813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136086135 | CAAGTCACCCCTGGG[A/G]ACCCTTGTTGGACAT | 138151 |
| rs558571847 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136094633 | GGGGCCCGAGTGGGG[C/G]AGGCGCGGGAGGCGG | 138151 |
| rs558582455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136038314 | GCCAAGGCCGGTGGA[C/T]TGCTTGAGCCCAGGC | 138151 |
| rs558602674 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013506 | GATGACCGGGTGATG[A/G]GGCTGCAAGGTGACC | 138151 |
| rs558607842 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136077144 | AGATTGCGCCACTAC[A/G]CTCCAGCCTGGGTGA | 138151 |
| rs558640237 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136095390 | CGCCGGCCGCGCGCG[C/G]GCGCGCACTGGCAGC | 138151 |
| rs558659369 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136078204 | CCCAAGGCCGGGTGC[A/G]TACCCACCACCTGGC | 138151 |
| rs558667937 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136067609 | TTGGGAAGCCAAGGC[A/G]GGCAGATCACGAGGT | 138151 |
| rs558685091 | snp | A/G | | | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015323 | GCAGCCCAGCACTGC[A/G]CTCGCCATCCAGAAG | 138151 |
| rs558698048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136037553 | AGCTCTGTCACTCAG[A/G]CTGGAGTACAGTGGT | 138151 |
| rs558748212 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136074152 | ACAAATAATTTGTTA[A/C]AAAATTAGCCAGGCA | 138151 |
| rs558761721 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008809 | CTCCCGACTCACGCC[C/T]ACCGTGGGACACATT | 138151 |
| rs558797402 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136091791 | TTTACAAATGATCTC[A/C]TCTCACCAAGAGCCA | 138151 |
| rs558809463 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136042743 | ACAGACACACACAGA[C/G]ACAGAGACAGAGACA | 138151 |
| rs558828723 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096194 | TCACTCCCACAGCAC[C/G]CTCAAGGGTCCTTGC | 138151 |
| rs558828726 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136072012 | GGAGGCCCAGGTGGG[C/T]GGATCACCTGAGGTC | 138151 |
| rs558830342 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136090980 | CTGGGCGGGCCCAGG[A/T]GCTCGCGGCCGCCCA | 138151 |
| rs558834812 | in-del | -/CACA | 0.00776185 | 0.0618116 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007466 | ACGCGCACACAGACG[-/CACA]CACACAGACGCACAC | 138151 |
| rs558840904 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136070046 | AGACAGACAATATTC[G/T]GGGCCAGAAAGAAAA | 138151 |
| rs558906272 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136084632 | GACTCAAACAGACGC[A/G]CACGCCACGTCCATA | 138151 |
| rs558945314 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136030010 | TGAAGCGACACCCCA[A/G]GGATCCTGTGACACA | 138151 |
| rs558965724 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015055 | CCTCTTCCTGCCATG[C/G]CCCGTCTCCTGCCCC | 138151 |
| rs559051601 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136024827 | GGGCTGCGATCCTGA[C/G]AACTGGGACCTGCCA | 138151 |
| rs559054896 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136084298 | CATGCCCCAGCCCCT[C/G]CTGTGTCCAGCCCTG | 138151 |
| rs559062999 | in-del | -/GGCCT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136055112 | GAAGGCTGAGATCCA[-/GGCCT]GGCCTGCCCTGCCCT | 138151 |
| rs559076043 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014437 | AGCCCCCTGAGTAGC[C/T]GGGACCACAGGCGCC | 138151 |
| rs559085228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136018816 | ACACACCCCCACCCC[C/T]GGTGCAGCCTGCTGT | 138151 |
| rs559092849 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006423 | GCCGCTAACAGGGAC[A/G]GGGTCCTGAGGGTGC | 138151 |
| rs559182636 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010162 | CCCCATCTTCCATGG[G/T]CCCTTCCTCCACTGT | 138151 |
| rs559205522 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007151 | TAAAAATCACAATCG[C/T]GTACGATGCTAACAA | 138151 |
| rs559238769 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136093297 | ATAATGCAGCCTCAT[C/G]CTTTAATTGGAAAAC | 138151 |
| rs559247873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136064036 | ACTCAGGCCTATAAT[C/T]CCAGCACTTTGGGAG | 138151 |
| rs559266771 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136030566 | AGTGAGCCGAGACTG[C/T]GCCACTGCACTCCAG | 138151 |
| rs559280357 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136059214 | AGCAGGGCCATTCCC[C/T]GGGACTAGGGACACC | 138151 |
| rs559291430 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011216 | GCACCAGGGGCCTGG[C/T]GGCCTCCCACCCTCC | 138151 |
| rs559309581 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136075042 | AGGCCCAGTAGAGGA[C/T]GTGACCTCCTCCAGG | 138151 |
| rs559368477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136055798 | AGGGGAGAGTCCCTC[C/T]ACCCCGAGCCCCGGC | 138151 |
| rs559394262 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009517 | AGTGCCTGCCCATGG[C/T]CCCCCACCTCCTTCT | 138151 |
| rs559409393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136020427 | GTGTCATCGGGGACT[C/T]GCCCAGGTGACACCA | 138151 |
| rs559416809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136021579 | TTCAACATACACTTA[C/T]GACCCAGCAATTATA | 138151 |
| rs559422017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136026212 | CAGGTGTGGTGGTGC[A/G]CACCTGTAATCCCAG | 138151 |
| rs559428515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015326 | GCCCAGCACTGCGCT[C/T]GCCATCCAGAAGCAG | 138151 |
| rs559430781 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136027014 | CAGGGGGATCACCCA[A/C]GGTCAGGAGTTCAAG | 138151 |
| rs559457921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136032256 | TTTATTCCAGGAATA[C/T]GAAGTTATTTCAATA | 138151 |
| rs559549449 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NACC2 | GRCh38.p7 | 9:136057104 | CAGCAGCAGGCTCTG[C/T]GTCCGATAGGGCCTT | 138151 |
| rs559551401 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136085633 | GGGGGTGGGTACAGG[C/T]GGGTGGCGGGCAGCC | 138151 |
| rs559553660 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NACC2 | GRCh38.p7 | 9:136021989 | TTGGCGAGGGAGCCA[C/T]TGTGAATGAGGAAAG | 138151 |
| rs559557420 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136066895 | CACAAGAGGGCACAT[A/G]TTATGAGATTCCATT | 138151 |
| rs559606815 | snp | C/G | 0.00279162 | 0.0372561 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009076 | GTCCTGGCCAAGGGT[C/G]GGGGGGCACCCACTT | 138151 |
| rs559612337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136065668 | AAAATTAGCCAGGAG[C/T]GGTGGCACATGCCTG | 138151 |
| rs559640392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136022421 | TGCTTCCCAGCTCCC[C/T]GCCCAGGTGCCTCCT | 138151 |
| rs559643300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136055195 | GGGTGAGAGGAGCCC[A/G]CGGGGAGGACAGGGG | 138151 |
| rs559679965 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136084690 | AGTGGCCCCAGGGTC[C/T]GCCAATGGGTGACAG | 138151 |
| rs559687760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136071330 | CTGGCAGATCACGAG[A/G]TCAGGAGTTTGAGAC | 138151 |
| rs559704700 | in-del | -/C | 0.00517822 | 0.0506191 | intron-variant | NACC2 | GRCh38.p7 | 9:136082016 | GCCAATCTGCCCTGG[-/C]CCAGGGCCTCCAACC | 138151 |
| rs559734403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136061243 | CAGGCCAGGACTCCT[A/G]ACACCCCAGCTGGAG | 138151 |
| rs559762892 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136080148 | CCACAAAAGCCAACG[C/G]TTTGACCACAAGGGC | 138151 |
| rs559789615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012295 | CCAGCTGTGAGGCTC[A/G]GGCCTGTTTTTAATC | 138151 |
| rs559803160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136032493 | GAGGAACAGTGGAAG[C/T]TTTTCCTGAGTTTAG | 138151 |
| rs559808587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136030071 | GTAGACATGGAGTTT[C/T]ACCATGATAGCCAGG | 138151 |
| rs559808686 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136024040 | TCCTCTGGGAGACAG[A/T]GTGTGTGGGGACAGC | 138151 |
| rs559826318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136017009 | GGCCACCTGACTCAG[A/G]GGCAAGGACACGGGG | 138151 |
| rs559826644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136066838 | ACGGATGAGCGCTAC[A/G]CTAAGCGAAACATTA | 138151 |
| rs559855968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136075925 | CCCCGCAGCCCTCCA[C/T]GTGCTCAGTGCCTGT | 138151 |
| rs559871010 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136086715 | AAACCCTCCCCGACC[A/G]GTGGCCCCGTTTCCC | 138151 |
| rs559945813 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136024568 | GTGTGTGTAAGGACA[C/G]AGTGTGTGTGTAAGG | 138151 |
| rs559996505 | snp | C/T | 0.0788843 | 0.182262 | intron-variant | NACC2 | GRCh38.p7 | 9:136043101 | AGGCTACAAAAAGCA[C/T]TAGCCGTAAAATACA | 138151 |
| rs559997481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136076352 | AGCCAGGTTTCCTGC[C/T]CATACCACGACAAAA | 138151 |
| rs560065520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136039068 | TGCAAATCCCAACCA[C/T]ATGCCGTCTCTAAAA | 138151 |
| rs560076952 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | NACC2 | GRCh38.p7 | 9:136064224 | AGCCCAGGCGATCGA[C/G]GCTGCAGTGAACTAT | 138151 |
| rs560169081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136081985 | GGAGCTGACGCGAGA[A/G]CCAGGCTGCAGCAAA | 138151 |
| rs560183531 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136019413 | CCTGAGCCTGGGTCT[C/T]GGGTACTGGGGGACC | 138151 |
| rs560196994 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136059918 | CCCACCCCGATGTCC[C/T]GACCAGCAGAGAGGG | 138151 |
| rs560210419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136070816 | AAAAGATCAATAAAG[C/T]TGACAAACATCTAGC | 138151 |
| rs560255589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136082493 | CAGGTGTGTGCAGGG[C/T]GGAGCTGACAGTGGC | 138151 |
| rs560258451 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136059342 | TGCACCAGCCCATCC[A/G]GAGCAGGGCCCTATG | 138151 |
| rs560293873 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136073940 | GCCCTGAAAGCAGAC[C/T]CTGGCTCTCACCGAA | 138151 |
| rs560309634 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136068726 | AATAAAGATGTCATT[A/T]CAAAAATAAAAACAC | 138151 |
| rs560339963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136092490 | TTGGAGGGCGCTCCA[C/T]GGCCTCACACCACAG | 138151 |
| rs560343815 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NACC2 | GRCh38.p7 | 9:136083915 | GGCCCAGGCAGCTCT[C/G]GGGCCCAGAGACAGA | 138151 |
| rs560362774 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136090379 | CCACAGCTGCCCCCT[A/G]ACTCTAGGCAGTGCC | 138151 |
| rs560380154 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136079098 | GGTATTAGTTTAGGG[A/C/T]ACGTAACCTGAAATC | 138151 |
| rs560389766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014220 | GGGGAAAGCCACAGC[A/G]CCCCCCACCCTCCCC | 138151 |
| rs560420596 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136020827 | CTTTTGACAAAGGTG[C/T]ACCAGCCTTTGTCAA | 138151 |
| rs560452546 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NACC2 | GRCh38.p7 | 9:136047149 | GCCTCCACTCCTGCA[C/T]GGCCTGGCGAGGGCA | 138151 |
| rs560561118 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136089743 | TTAGGAGCCACGGCC[A/G]ACCACTCAACCTCTA | 138151 |
| rs560573557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136066347 | ATAGGCAAGGCATCT[A/G]AAAAGGTATTTCTCC | 138151 |
| rs560587716 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136087429 | TAGACACCCTGCCCT[A/C]CTGGAGCTGGCAGAC | 138151 |
| rs560618633 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136045691 | ACCTCAGCGGTCTGC[C/T]ATGCCACAGGTGCCC | 138151 |
| rs560629263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136031375 | TAGAGTCTTGCTCCA[C/T]CACCCAGGCTGGGGT | 138151 |
| rs560716557 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136021431 | CTCACCTCCCAGTGC[A/G]GCGAAACATAAAAAC | 138151 |
| rs560782193 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136085003 | TCTAGAGATGGTGCT[A/G]AGGGCAGCGCAAAAA | 138151 |
| rs560787397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136084772 | AGAAGGGACGGGCTC[C/T]GCCACTCCCTGCAAC | 138151 |
| rs560799853 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136056341 | CGGCCAGGAACTCCC[A/C]CCAACCCCGAGGCCC | 138151 |
| rs560840461 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012223 | TGGGAGGCCTCCCCA[C/G]CCCATTCCTCTGGAA | 138151 |
| rs560865911 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007076 | TATTTATACATTTTA[C/T]ACTTAGTTCTTTTTT | 138151 |
| rs560913937 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136030972 | GGCCAATACATCTCA[A/G]CTTTAGACGGAGCCG | 138151 |
| rs560947890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136081241 | GGACTCAGTCCCGAC[A/G]GGCACTGGGGGCTCC | 138151 |
| rs561059813 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136083779 | CACCTCTCCACCTGT[A/T]AGTGGTGGCACGTTC | 138151 |
| rs561103628 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136056763 | GGCTCTCTCCGTTCA[C/G]CCAGGTCCCTAGGCG | 138151 |
| rs561114900 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008355 | GGAGAGGCGGCTAGA[A/T]CCCAGGCCCACCACC | 138151 |
| rs561132914 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136058263 | CCCAAAGGGCGAACT[A/G]CAGGGCAGACACCCG | 138151 |
| rs561136608 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136076786 | GGCTGAGGTGGGTGG[A/C]TCATGAGGTCAGGAG | 138151 |
| rs561169167 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136033723 | GAGAACTACAAAATA[G/T]TCCTAAGAAAAAATT | 138151 |
| rs561174651 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136089917 | AAAAGTTGTGTGATA[C/T]GGATTTCATTAACAT | 138151 |
| rs561190617 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136056471 | AGGCCCCTAGCCATC[A/G]TCCTTCCTGGGTGGT | 138151 |
| rs561227930 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008990 | GCACGGGACATTGTG[C/T]GGGCCTGAACAGCAG | 138151 |
| rs561295419 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136028971 | CACAAGAGGGAGGCC[A/G]AGGTGGGGCTAACAG | 138151 |
| rs561295921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013652 | TGGGGGTTGCATCCA[C/T]AAGCCCGTTTGAGAA | 138151 |
| rs561380538 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136074890 | CAGCCGAGGCGGAGT[C/T]GGCAGGGCCGGGGGA | 138151 |
| rs561427701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136062796 | GTGGTGTGTGACTGT[A/G]GTCCCAGCTGCTTGG | 138151 |
| rs561428700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136017843 | GGCTCCTGCACACCC[C/T]ACCGAGCGCAAGGCC | 138151 |
| rs561429274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067696 | AAAAATTAGCCGAGC[A/G]TGGTGGCGGGCACCT | 138151 |
| rs561441830 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136090637 | TTCCAGCCTCCAGAT[G/T]CCAACATCAGCTCCT | 138151 |
| rs561470286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136072337 | GATCACTTGAGGCCA[A/G]GAGTTTGAGATCAGA | 138151 |
| rs561489607 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136067498 | TTGTTCTCTGAACAC[C/T]GCAGGTGATTTTGTC | 138151 |
| rs561502690 | in-del | -/CACT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067793 | GAGCCGAGATCGCGG[-/CACT]CACTGCCTCCAGTCT | 138151 |
| rs561520461 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010915 | CAGCCATCACTGCCC[C/T]CTCACCACACCCCTG | 138151 |
| rs561555348 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015298 | CCCAGGGGCCCACCC[A/C]GCCGCCCCGGCAGCC | 138151 |
| rs561610915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136057838 | GGGGGTTGTGGAAGC[A/G]GTCGGATCCCAGGCA | 138151 |
| rs561633820 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011162 | TTCGTCTTCCGGGCA[A/G]GAGGAGCAGGAAGGG | 138151 |
| rs561693455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136031043 | AGAGGAAATAGATTA[C/T]GTGAACTATTCCTGC | 138151 |
| rs561713962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136074802 | GTTCCCAGCTCACCT[A/G]CGGGGCTCGGGGATG | 138151 |
| rs561724507 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136078511 | TACTGTACAGATGAG[A/G]AAACTGAGGCTTGGA | 138151 |
| rs561751112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136025138 | CTGGGGAACACCAGG[C/T]TTTCAGCTGAGGCCC | 138151 |
| rs561787002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136093018 | GCCCCACTGACGGTG[A/G]CTGGGGCCACTGGGC | 138151 |
| rs561811507 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136060659 | CCACATGCTTAGCCC[C/T]GTCGGGTCTCAAAGG | 138151 |
| rs561837726 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136026438 | ACTTGGGGAAAGCCT[A/C]ACATACATGTAACTG | 138151 |
| rs561839696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136032198 | GCGAGCTGCATCCAG[A/G]GGCATGTATAACAGA | 138151 |
| rs561877615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136069481 | TTGAAACCAGAAGGC[A/G]GAGGTTGCAGTGAGC | 138151 |
| rs561892505 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136057694 | TCCCCTGCACCGGCT[C/T]GGCCGGGTGGAAGCT | 138151 |
| rs561902503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136051888 | GGCAAGGAGGAGGAG[A/G]AGGAGGAGGAGGAGG | 138151 |
| rs561973851 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136026985 | TGTAATCCCAGCACT[C/G]TGGGAGGCTGAAGCA | 138151 |
| rs562029761 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136092687 | GAAGGTGGACTGGGC[C/T]GGAGGAGCAGCAGAG | 138151 |
| rs562037702 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136083726 | CTTTTGGCCTCCACC[A/G]CTGTGCAAGAAGAAA | 138151 |
| rs562039715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136088771 | GGCCACAGATGAGGG[C/T]TCAGGCCTGGGCGTG | 138151 |
| rs562056662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136060076 | CCGCATCTGCCCTGG[C/T]GGCATGCCCAGACCT | 138151 |
| rs562080079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136070549 | AAAAATACAACATAC[C/T]AAAGTTTGTGGGACA | 138151 |
| rs562108406 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136057470 | GTCCACACACTGTGG[G/T]ATGCTCCCTCACACC | 138151 |
| rs562109628 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136021956 | TGCGGACAAGCCTCA[A/C]GGGCAGCATGGAGGG | 138151 |
| rs562127955 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136084350 | TTCACCAAAGGCGGG[C/T]TGCTGGAGGGCTGCT | 138151 |
| rs562142720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136075813 | TTGGGCTCTGAGGCT[C/T]GGGACACAAGATTCA | 138151 |
| rs562175876 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136079626 | CAGAAGAGAGGCCAG[A/T]GGCCCCCCAGAGCTC | 138151 |
| rs562213736 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136071245 | ACGTCTCAAAAAAAA[-/T]AAAGTAAAATTTAAA | 138151 |
| rs562217158 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136055718 | TTCTGGACCTCAGCA[A/C]ATGCACAGCCATTAA | 138151 |
| rs562234053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136038401 | AAAAATTAGCTGGGT[A/G]TGGTGGCATGTGCTT | 138151 |
| rs562240139 | snp | C/T | 3.33222e-05 | 0.00408167 | synonymous-codon, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016275 | CTCACCTGCCACCAG[C/T]TCCAGCTTCTCCCCG | 138151 |
| rs562397527 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136078803 | GGTCCCCAGTAAGCA[A/C]CCCCAGCGTGGTCCC | 138151 |
| rs562430203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136076253 | GCCCTGCGGAACTCG[A/G]AGAAGTGCTGTAACT | 138151 |
| rs562444984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136057822 | CATCACCACTGGGGC[C/T]GGGGGTTGTGGAAGC | 138151 |
| rs562455431 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NACC2 | GRCh38.p7 | 9:136090992 | AGGAGCTCGCGGCCG[C/T]CCATGGCCCTGTGCC | 138151 |
| rs562455596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136085897 | AGCCCAGAGGCCGGG[C/T]GCCGTGCAGGGCAGC | 138151 |
| rs562470497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136073216 | GAGGATCACTTGAGC[C/T]CAAGAGTCCAAAACC | 138151 |
| rs562507235 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008278 | CCGGTCCCTCCTGGA[A/C]CTCTCCATGCAACCC | 138151 |
| rs562541082 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136086222 | CAGAGCAGCAAAGCG[C/T]AGTGCCTGCCTTCCT | 138151 |
| rs562556482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136073860 | TCTGCTAAAATGCTG[C/T]CTGGTCTTGGAGTAT | 138151 |
| rs562654440 | in-del | -/AG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136059530 | GTGTGTGGTCCACTC[-/AG]GGAGCTGGGGGGTTG | 138151 |
| rs562668527 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136077934 | ATAGTTTTGTTTTGG[G/T]TTTTTTTGTACTTCT | 138151 |
| rs562692787 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136077639 | CCAGAACAGGCCCTT[C/T]ACAGAGGAGAAGGTC | 138151 |
| rs562729361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136087384 | AAAGCCCCTTCCCTC[C/T]TCCTGGCCTGTCACC | 138151 |
| rs562750200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136018901 | CAACAGAAATAATTC[C/T]CCATCCACAACCACC | 138151 |
| rs562770381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136018268 | GCCTCGGGGCGTGGG[A/G]GGGCTGCCAAGGGGG | 138151 |
| rs562781428 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136086918 | CTCCCACACCACACC[A/G]GGGGTTCGCATCTAC | 138151 |
| rs562800216 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136097232 | TTTTTTTTTTGAGTC[C/T]GAGTCTCACACTGTT | 138151 |
| rs562816907 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136082967 | AGATATCAGGGCGAG[A/G]GGGAAGACGCCGTGT | 138151 |
| rs562843587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014150 | CACCAGGAGAGGCCA[C/T]GGCCAAGGCCAGCCC | 138151 |
| rs562865530 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136092181 | CTCTGGGAGGACCAA[A/G]GGCGTGCCCAGAGAG | 138151 |
| rs562882468 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013784 | TGCCACAACCCTGGA[C/T]GATCAGACAGCTCAT | 138151 |
| rs562896137 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136077044 | AAATAGCCGGGTGTG[A/G]TGGCGGGCGCCTGTA | 138151 |
| rs562900699 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136070490 | CCAGCCTGGGCGACA[A/G]AGCGAGACTCGTCTC | 138151 |
| rs562918512 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136058958 | GTAGCAGAGGCCCAG[A/G]TGTGGGAGGCGTGAC | 138151 |
| rs562952829 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136091586 | ATGACAAGCAACCAA[C/T]ACTTCCAGACAGATG | 138151 |
| rs562962184 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136075727 | CCCCGTGCAGACTGC[A/G]CCCAGGGGAGGAGAC | 138151 |
| rs562966752 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024922 | CCTCGGGGCCCAGGA[C/T]CCTGAGAGCCGGCCT | 138151 |
| rs562981408 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136058626 | AAAACTAACCCACCG[G/T]GTACCATGCTCACCA | 138151 |
| rs563006813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136093323 | AAAACAAAGGGAGGA[C/T]TGAAGAATTTTTTAA | 138151 |
| rs563015492 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096600 | CACAGAGTCCCATCT[A/G]GACCTAAATGCAGTC | 138151 |
| rs563021979 | in-del | -/CGC | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136078969 | GCCGGCATGATGCCG[-/CGC]CGCCGCCGCCCCTCT | 138151 |
| rs563075105 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010260 | GCCCAGGCCTGTCCC[A/G]GTCATCCCCTGCCTG | 138151 |
| rs563088328 | in-del | -/AAAAC | 0.073099 | 0.176652 | intron-variant | NACC2 | GRCh38.p7 | 9:136069553 | ACTCTGTCAAAAAAC[-/AAAAC]AAAACAAAACAAAAC | 138151 |
| rs563127798 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136026165 | GCTAACATGGCAAAA[C/T]TCCGTCTCTACTAAA | 138151 |
| rs563129577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136089318 | TCCTGAGGTCCCCAC[A/G]GCCCTAGGAGGGAGA | 138151 |
| rs563176985 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136045444 | TGTCAATACCCAGGC[A/G]TGGCTTTGTCTCTGC | 138151 |
| rs563190853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136064645 | TAAGGAATATGTCCC[A/G]AATTTATCTACAGAC | 138151 |
| rs563216187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136061372 | GAGGCACAGCCCTCA[A/G]ATAGAGGGGTCCCCT | 138151 |
| rs563218672 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136027774 | AGGCTGAGGTATCAA[C/T]GATCTACAGATCTCT | 138151 |
| rs563228054 | snp | A/C/T | 0.000102464 | 0.00715693 | missense | NACC2 | GRCh38.p7 | 9:136011770 | GAGCCACGATGGTGG[A/C/T]GGCGTCGCCCCGCCG | 138151 |
| rs563338628 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007280 | AAACAAACACGAAAA[A/C]CCTTTGCCATTTTAG | 138151 |
| rs563375977 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136066700 | AGTGTCCTAGCAGTA[A/T]CATTTGCAATAGCCA | 138151 |
| rs563399076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016141 | TAAAAGGAAATTAGA[A/G]GAAATTTAAGATTTT | 138151 |
| rs563413727 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136028398 | TTTTTTTTTTTTGAG[A/G]CAGGGTCTCTTTCTG | 138151 |
| rs563448003 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014838 | TGTGCTGTTTACCCT[C/T]GGAAACTTGACCACA | 138151 |
| rs563458064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136079336 | CAGGCCTGATGGAAC[A/G]GGGTGCCATCCTCTG | 138151 |
| rs563461739 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007562 | ACGCACACACACACA[A/G]ACACGCGCACACGCA | 138151 |
| rs563463782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136061746 | GCCAGGTGGGTGGGC[A/G]GGGACAAGCACATGA | 138151 |
| rs563495910 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136052881 | CAGGACTTGTGGTGG[-/C]CCCGGGACCCCTCCA | 138151 |
| rs563500101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012122 | CTGGATGAGCCTCCC[C/T]GGCCGCTCCTGGGGC | 138151 |
| rs563554030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136017440 | CATGCACCAGGTGCG[C/T]GGGGCCAAGGAAACA | 138151 |
| rs563564826 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136032645 | CTCACGTAGGTAATC[C/G]CAGCAGTTTGGGAGG | 138151 |
| rs563637647 | in-del | -/TT | 0.425894 | 0.177655 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136097208 | AGCTCTGTTTATTCC[-/TT]TTTTTTTTTTTTTTT | 138151 |
| rs563662297 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136076372 | CCACGACAAAAATGA[A/G]ATGAAATTCTGATGC | 138151 |
| rs563664772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136017819 | TAGGGAATCAATCCC[A/G]CTGCCCTGGGCTCCT | 138151 |
| rs563686102 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136067185 | CTTGAACCCGGGAGG[C/T]GGACGTTGCGGTGAG | 138151 |
| rs563692279 | snp | A/C | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007270 | GAAACAAAACAAACA[A/C]ACACGAAAAACCTTT | 138151 |
| rs563801514 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136076746 | CCTGGTGGTGGCTCA[C/T]GCCTGTAATCTCAGC | 138151 |
| rs563815057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136028583 | TGTAGTGGGTGAGGC[A/G]TGGCCAGGGCTGCAC | 138151 |
| rs563869187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136062370 | ATGTCAGCTTTTGTC[C/T]AGGAAACATGCAAAG | 138151 |
| rs563888706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136071894 | GCTGGGGCAACTGAA[C/T]GTCCAGACGCAAATG | 138151 |
| rs563919694 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136082944 | GTGCTGCCTGCCTCA[A/C]TCCTGCCAGATATCA | 138151 |
| rs563932143 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136087238 | AGATGCACAGAGTGT[C/T]AACTCCGGGCCTGCA | 138151 |
| rs563969538 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078969 | GCCGGCATGATGCCG[C/T]GCCGCCGCCGCCCCT | 138151 |
| rs563987757 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136062753 | AACCCCATCTCTACA[A/T]AAAAATACAAAGACT | 138151 |
| rs564014943 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136067459 | GGGGATATATCCTGA[A/G]AAATGCATCATTAGG | 138151 |
| rs564023698 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136025041 | CAAGAAACGAAAAAA[A/T]CAAGGAAATCTAGAA | 138151 |
| rs564036326 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136030481 | CAGGCATGGTGGCAG[C/G]CGCCTGTAGTCCCAG | 138151 |
| rs564067829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136020148 | GTCACTGCAACGGCC[C/T]CTCTCACGTCCACTT | 138151 |
| rs564081584 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136030100 | GGCTGGTCTTGAACT[C/T]CTGACCTCAAGTGAG | 138151 |
| rs564115959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136082548 | CATGAAGCACTGGGT[C/T]TGGCCCTCGGAGCCC | 138151 |
| rs564200531 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136078443 | ATGGCAATCCTTAAT[A/T]CAGGTTTTTCCATTT | 138151 |
| rs564217810 | in-del | -/AC | 0.00716266 | 0.059414 | intron-variant | NACC2 | GRCh38.p7 | 9:136042714 | CACACAGACACAGAG[-/AC]ACACACACAGACACA | 138151 |
| rs564260981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136068831 | GAATCAAAAACTAAA[A/G]TAGGAGACAAGGCCT | 138151 |
| rs564288980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136047786 | ATCAAGGCAGGTGGG[C/T]GTGAGGGCTTCTAGC | 138151 |
| rs564290636 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136074620 | TCGTTCTGTCACAGC[A/G]AGGCTGCCTGCCTTC | 138151 |
| rs564328739 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010826 | GCTGCAGAGCCGAGA[C/T]GGATCGGGCAGAACA | 138151 |
| rs564349163 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136081307 | AACTGTAGAGTAACC[A/G]GAACGACCTGCACAC | 138151 |
| rs564393999 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010388 | TGCCTCCTGCCCGAG[C/T]GGAGTCCCCCGCTCC | 138151 |
| rs564429383 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136069141 | TCAAACTCCTGACCT[G/T]GTGATCTGCCCGCCT | 138151 |
| rs564437943 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136018678 | TGCACAGCCCCTGCC[C/T]GGCCACTACAGGGGT | 138151 |
| rs564441990 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067759 | AGAATCACTTGAACC[C/T]GGGAGGCGGAGGTTG | 138151 |
| rs564519271 | in-del | -/G/GGG | 0.0327262 | 0.124425 | intron-variant | NACC2 | GRCh38.p7 | 9:136058105 | TCAGCCACTGGGGGC[-/G/GGG]GGGGGGGGCCCAATG | 138151 |
| rs564559357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136061876 | TGTAATCCCAGCACT[C/T]TGGGAGGCCAAGGCG | 138151 |
| rs564574858 | snp | A/T | 0 | 0 | intron-variant | NACC2 | GRCh38.p7 | 9:136083431 | CCCCTGTACTAGGAA[A/T]AGCATCTCTCCAAAA | 138151 |
| rs564581043 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136085210 | GCTGGAGTGCAGTGG[C/T]GCCATCTCAGCTCAC | 138151 |
| rs564710041 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136090082 | ATGAAATTAAATGAG[C/G]AAAACTCTGTTAAAG | 138151 |
| rs564721695 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136020882 | ATGGGGCTTGAGCAA[C/G]TGGCCATCCGCACCC | 138151 |
| rs564743540 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136081022 | AGAGGTGATGGAGGA[G/T]GAAGTTTTCATCCCA | 138151 |
| rs564806730 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136077051 | CGGGTGTGGTGGCGG[A/G]CGCCTGTAGTCCCAG | 138151 |
| rs564815463 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136034856 | CCCAGCATTTTGGAA[G/T]GCACTGGCGGGCCGA | 138151 |
| rs564841109 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007923 | CTCAGAGGGGGACCA[A/G]CCCTCCCTCCCTACC | 138151 |
| rs564877339 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007677 | GCTACGAGCTCTGGA[A/T]TCTGCGCTTAGGACT | 138151 |
| rs564899616 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067376 | GGTTTTTGGAGTGAT[A/G]AAGATGTTCTAAAAT | 138151 |
| rs564903119 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012714 | AGTGCTTCTTGGGCC[A/G]AGGGCCACAGGAGGC | 138151 |
| rs564904411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136028727 | CAGACCTGAGCATCT[C/T]TGCACTCTTGGGGGC | 138151 |
| rs564914965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067168 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCGGGAG | 138151 |
| rs564919740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136094072 | TGCACGCGCTCCCGG[A/G]GGCAGCTCCACGGGA | 138151 |
| rs564944378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136090413 | GAGTGAGAAGGTAAC[C/T]CCTCCAGAAAACACC | 138151 |
| rs564995304 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136095721 | GGCCCCCCTACCCCG[C/T]CCCCGGCGCGCGCCC | 138151 |
| rs565029502 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136029673 | CTTCCAGGTGCCACC[A/G]TGTTTCCCAGTGTCA | 138151 |
| rs565056730 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136077756 | CCGGGGAGCAGGCAA[A/G]GGGGCAACAAAATTG | 138151 |
| rs565060809 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136037230 | TATTTTTATATAAAG[A/T]TTTTTCTTTTTTTGA | 138151 |
| rs565096086 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136085762 | TAAGTTTAATTACTT[C/T]ATCTTTTACCTTTTT | 138151 |
| rs565131486 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009755 | TGGTCCTCCCCTAGC[A/G]GAGGCGGCCTCCGCT | 138151 |
| rs565138034 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136030824 | ACACCTCCATGCCTG[C/G]CTAACTTTTTGTATT | 138151 |
| rs565143254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136072405 | ACAAAATTAGCCGGG[C/T]GTGCTGGTGTACACC | 138151 |
| rs565175170 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136023556 | ACCCACTCCTACCAG[A/C]ACCAAGCCTGGTCCT | 138151 |
| rs565193934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136029070 | GGGGTGGGTCCTGGT[A/G]AGCCCTACCTTCAAG | 138151 |
| rs565265483 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013356 | AGGGTACCTGGAGGC[C/G]ACCCGCCCGCACGAA | 138151 |
| rs565294401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136063566 | TTCCTACCTGGGAAG[A/G]GTATGCACAAACAAG | 138151 |
| rs565295879 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136017908 | CCCGATTGCACGAGG[A/G]CAGCCTGCAGGTGGG | 138151 |
| rs565302442 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009627 | TAGAGGCGGCCCCAC[A/G]GGAGGTCTCCTAGGG | 138151 |
| rs565341272 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014053 | TGGGTGAGGGGGAGG[G/T]GGGGAGGTGGAGGGG | 138151 |
| rs565370792 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013731 | GTCCTGGGGCCGACC[A/G]GCCACGGCTGAAGTC | 138151 |
| rs565379757 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074079 | GGGAGGCTGAAGCAG[A/G]AGGATCACTTGAGTC | 138151 |
| rs565408050 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136018237 | AGTCACAGAAAAACT[A/C]TACAGGGGTGGCTGA | 138151 |
| rs565411435 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067745 | AAGGCTGAGGCAGGA[C/G]AATCACTTGAACCCG | 138151 |
| rs565467227 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010480 | CCCCCAGTGGGAGAC[A/G]AGTGGTCCCTGGCCC | 138151 |
| rs565486834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136042442 | ATAGGCCTGCAGGTA[C/T]GTATTCGACTGATTC | 138151 |
| rs565557123 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015023 | GCCTGCTTCCAGGAG[C/G]CTGTGAGTGCCCATG | 138151 |
| rs565564711 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | NACC2 | GRCh38.p7 | 9:136043121 | CGTAAAATACAACTT[C/T]AATAAATTGATCTTC | 138151 |
| rs565629492 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136062264 | ATACTTCCCCCCAAC[A/G]CCAAGGGACCACCCA | 138151 |
| rs565687845 | in-del | -/AAAAT | 0.0341408 | 0.126114 | intron-variant | NACC2 | GRCh38.p7 | 9:136033176 | TGAGACCCTGTCTCA[-/AAAAT]AAAATAAAATAAAAT | 138151 |
| rs565698454 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136048951 | CTGCATGCAGACCAG[C/G]CAGGTGGCCAGCCCA | 138151 |
| rs565703272 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136081315 | AGTAACCGGAACGAC[C/G]TGCACACCACACACC | 138151 |
| rs565707319 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136026615 | AGCATGGGGAAAAAA[G/T]GTGCAGATAAATATA | 138151 |
| rs565719049 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136083588 | AACGCGGACACCTGT[G/T]AAGAGCGCCGTGCAG | 138151 |
| rs565788350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136092222 | AAGGAACGAAATGCT[A/G]GGGAGAGGGCACTTC | 138151 |
| rs565826123 | in-del | -/AG | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136055206 | GCCCGCGGGGAGGAC[-/AG]GGGCTCACTGGAACT | 138151 |
| rs565844287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136021173 | ATATAAAGAAATCTC[A/G]ATACTCAACAGTTAA | 138151 |
| rs565882583 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136031597 | CCCGCCTCGGCCTCC[C/G]AAAGTGCTAGGATTA | 138151 |
| rs565892091 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | NACC2 | GRCh38.p7 | 9:136046655 | TGCATGGCGCCTTCT[C/T]GCAGCTTTGCTCCTG | 138151 |
| rs565947292 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136031957 | TGTTAACAGCTTTCC[A/C]GATGCTAGGGCCTGG | 138151 |
| rs565949254 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136083402 | AGTGGGGCAGGTGGA[C/T]ACTTTGGCCTTCACC | 138151 |
| rs565949752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136079331 | ACCTTCAGGCCTGAT[A/G]GAACGGGGTGCCATC | 138151 |
| rs566060876 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136075567 | GTGCCTGAGGACGCA[G/T]CTTCTTTTATCGGGC | 138151 |
| rs566065595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136061547 | GCGGATGGATGGGCC[A/G]TGCTGATTGTACCCA | 138151 |
| rs566149802 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136065880 | TTTAAAAATCTTGTG[C/T]TTCAAAGAATACCAT | 138151 |
| rs566236883 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136023649 | TTGCTGATCTGATGG[A/C]ATCCCTTTCCTGCTC | 138151 |
| rs566293621 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136029946 | GAGCCCAGCAGGCAC[A/G]AGCAAAACTTGGGTA | 138151 |
| rs566300681 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136094291 | GAGGCCAACTCCAGG[A/G]ACCCGGCCTCGCGGC | 138151 |
| rs566329398 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136067789 | GCGGTGAGCCGAGAT[C/G]GCGGCACTGCCTCCA | 138151 |
| rs566337555 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136067576 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 138151 |
| rs566369100 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007419 | CGTGCACACAGACGC[A/G]CGTGCACACATACAC | 138151 |
| rs566390912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136076913 | TACTTGGGACTAGGC[A/G]GAGAATGGCGTGAAC | 138151 |
| rs566445776 | in-del | -/GGTGAGGCCACTCTGTGCCG | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016553 | GCCCACCTGGGCCCA[-/GGTGAGGCCACTCTGTGCCG]CTCTCCTGCTGGCCT | 138151 |
| rs566446968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136077095 | TGAGGCAGGAGAATC[A/G]CTTGAACCCGGAGGT | 138151 |
| rs566466069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136063272 | GGAGCAACGCACCAG[C/T]GAGGGGGCCCTGGAG | 138151 |
| rs566518847 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NACC2 | GRCh38.p7 | 9:136017995 | CCCTCGGCAGCCTCA[A/G]TGTGATGGGAAGTCC | 138151 |
| rs566520511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136070133 | ATCAAACTAGAAATC[A/G]TAACAAAGGTAACAG | 138151 |
| rs566559727 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136073344 | CTGAGGTGGGAGGAT[C/T]GCTTGAGCCTAGGAG | 138151 |
| rs566569540 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136018435 | TGAATCCACAGCGGG[C/T]GCCCCACTGAAGGCA | 138151 |
| rs566581428 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136082654 | CCCGCGCTGCCTCCA[A/C]GGACCTGCCTCCCAA | 138151 |
| rs566585183 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008949 | CAGAACAAAACAGAC[A/G]GCGATTACAAACGAG | 138151 |
| rs566636718 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136086944 | TCTACCTGACCCTTT[G/T]AATGCGGCCTTATTT | 138151 |
| rs566685645 | snp | C/T | 0.00101881 | 0.022547 | missense, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013955 | GCTGGCCGCGTGTGA[C/T]GTAGACCCCAGAGCC | 138151 |
| rs566690872 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136063032 | CAAGAGAAGAAGCCC[A/G]ACTTTGCCGTCACTG | 138151 |
| rs566706635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136078652 | CCCAGCCCCGACATC[A/G]GGACAGAAAGGGGCG | 138151 |
| rs566707517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136094971 | CCCCCCGGCCCCGCC[C/T]GGCCCCCCTCCGCGG | 138151 |
| rs566722365 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136086054 | GCCCGGAGTCCGGGC[A/G]CCACGCAGGGCAGCT | 138151 |
| rs566750282 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136091206 | GCTTCACTGGCCCAA[C/G]AGCCCCCAGGCCAGC | 138151 |
| rs566754273 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136018881 | CATTTACATAAAGAG[A/T]TCACCAACAGAAATA | 138151 |
| rs566754520 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136018999 | CCTGCCCAGCTCCCC[A/T]AGAGCCAGAGACTGT | 138151 |
| rs566768771 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009367 | GGCTCCCTCTAGGCT[C/G]GGTGGTTCTTAGTTC | 138151 |
| rs566776901 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136095978 | GCACTGGGGCGTTGA[C/T]AGTCATTCCGGCACC | 138151 |
| rs566780454 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136091646 | AGACCCTATACAAGG[G/T]TGTGTGCTTCCAAAA | 138151 |
| rs566801643 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008765 | AGCACACAGCAGGTC[C/T]GCTCAGCAGCCACGC | 138151 |
| rs566816363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136042667 | ACACACAGAAACACA[C/T]ACAGACACACAGACA | 138151 |
| rs566870697 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136086956 | TTTGAATGCGGCCTT[A/T]TTTGGAAACAGGGTC | 138151 |
| rs566888426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136086557 | GCCACGGTCCCACCC[C/T]GGGCTCCACTGTGAC | 138151 |
| rs566895386 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136043601 | ATATACAGGATCTAC[C/T]GCTGCACGGTCTCAC | 138151 |
| rs566944779 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136037293 | CAGTGGTGTGATCTC[A/G]GCTCATTGCAACCTC | 138151 |
| rs566954519 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136030286 | TCAGAGGAGGCTCAT[A/C]CCTGTTGTAGACATT | 138151 |
| rs567008551 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136019650 | CACGACGAGAGGGCC[C/T]GGAGCAGCAGCCTCC | 138151 |
| rs567016026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136029973 | GGTAAAGGCACCACC[A/G]GCCACAGAGGTTTCT | 138151 |
| rs567106975 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014426 | CCTCCCACCTCAGCC[C/T]CCTGAGTAGCCGGGA | 138151 |
| rs567111597 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136055490 | GGCCCAGCCAGGCAG[A/C]TCCATGGTCTGAGGG | 138151 |
| rs567125163 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136068380 | GGTGTGTGCCTGTAA[A/T]CCCAGCTACACAAGA | 138151 |
| rs567177986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136025216 | CCTTGGAGAATGTGG[A/G]CACGGGCGCTGCTGG | 138151 |
| rs567213021 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136061479 | AGGGGCCCATGGCAT[G/T]TGGCCGCAGGAAGGG | 138151 |
| rs567284612 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136093363 | CTAGCCCCCTGCCCA[C/G]GGCAGAGCAGCCCTG | 138151 |
| rs567298659 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008711 | CCTCTGAGCCCGGGC[C/T]GCCGCCCCCGCCCCA | 138151 |
| rs567349003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136032367 | AAGCTTTTGTTACAA[C/T]GCAACACTTACGAGG | 138151 |
| rs567368853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136088901 | GAAGGTTTCCCGGAG[A/G]AGACAGCAGGCAATT | 138151 |
| rs567387914 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136027235 | GTCTCAAAACAAACA[A/C]AAAAAATTAATGTTT | 138151 |
| rs567421571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136071043 | AAGACCAGTCTGGCC[A/G]ACACAGTGAAACCCA | 138151 |
| rs567436742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136027181 | AGTGAGCCGAGATAG[C/T]GCCACTGCCCTCCAG | 138151 |
| rs567453476 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012334 | CTTCCGTAGCCCCAA[A/C]GGCTAACGGGAACTG | 138151 |
| rs567454329 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136021702 | GGCTAGACGCAGCCC[A/G]GATGTCCTGCAATGG | 138151 |
| rs567524429 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136076493 | GGGCACAGAGCAGGA[C/G]AGTTCAGAGACAGGA | 138151 |
| rs567544617 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136022238 | AATGTGGGGGCACCA[A/C]AGACGGGTGACCAGG | 138151 |
| rs567564725 | snp | C/G | | | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014569 | GCTGGGATTACAGGA[C/G]GAGGGGCACTGCACC | 138151 |
| rs567578132 | snp | C/G | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012233 | CCCCACCCCATTCCT[C/G]TGGAACAGTCTCTGG | 138151 |
| rs567601013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136028886 | GGCCAGGTGTATGTG[C/T]GCTCAGGGCAGTGCT | 138151 |
| rs567639458 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136035427 | CCTAAAGAGAGGGAC[A/G]TTCTACAAAATAATG | 138151 |
| rs567658636 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136093866 | CTAACTCTAGGCGCC[C/G]CTGCTGGGGGGTGCT | 138151 |
| rs567741758 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136094239 | TCCAATCCGGAGGCC[A/C]CGCGCGGGGGTTGGG | 138151 |
| rs567756359 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136084406 | ACCTCCTACGCAATG[G/T]CCGGTCTCCGCTGGT | 138151 |
| rs567783705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136056440 | TGAGACCTCACAGTC[A/G]GGAGGCAGCGGGGCC | 138151 |
| rs567786845 | in-del | -/A/AA | 0.215144 | 0.247558 | intron-variant | NACC2 | GRCh38.p7 | 9:136089985 | AATGGATTTATATCC[-/A/AA]AAAAAAAAAAAGAAT | 138151 |
| rs567796331 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067232 | ATCGCACACAGCCAA[G/T]AGCTAGCCTAAGCAA | 138151 |
| rs567796755 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136061979 | ACAAAAATTAACTGA[C/G]CGTGGTGGTGTGCAC | 138151 |
| rs567881947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136062576 | ATGAGTTAAATACAT[A/G]ATACCTGTTCTCTGT | 138151 |
| rs567975522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136085553 | ACTCAACAAGTAACT[A/G]TACTGAGGGGTCTGC | 138151 |
| rs567994837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136030849 | TGTATTTTTGGTAGA[A/G]ATGGGGTTTTGCCAT | 138151 |
| rs567995539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136035349 | CACTGAGAAGGTTCC[A/G]CTGCTGTGAATTGCA | 138151 |
| rs568021346 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136090528 | TTGTGGGGTGGGGGC[C/T]GGGTTGCTAGCAAGT | 138151 |
| rs568052128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136068225 | TTGTGTGGCTGGGCG[C/T]AGTAGCTCATGCCTG | 138151 |
| rs568054966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136046600 | TGCCTCGCTGCGGGT[A/G]GGGGGGCTTGAACTC | 138151 |
| rs568116137 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136059555 | GGGGTTGCCGAAGTC[A/G]GCTAGACGTTAAACA | 138151 |
| rs568136696 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136091700 | AGGAAGGCCACAGCT[A/G]AGGGAGCTAGGGCTC | 138151 |
| rs568147266 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136097040 | CGGATAAGCAGAAAT[A/C]AATTCCCCAATTTCT | 138151 |
| rs568189373 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NACC2 | GRCh38.p7 | 9:136092133 | GTAGAGAAACGCTGG[C/G]CAAGCTCCCCCACCC | 138151 |
| rs568277084 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136076476 | GGGTTCCACTCACAC[A/G]CGGGCACAGAGCAGG | 138151 |
| rs568310893 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136087992 | TCTGCTGGGAAGTTC[C/T]GGGAGGTGACCTGGG | 138151 |
| rs568314000 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136065386 | GCACTTTGGGAGGCC[A/G]AGGCGGGCAGATCAC | 138151 |
| rs568328512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136069792 | AATCCTAAATGTCCA[C/T]GTACCAGACAACGGA | 138151 |
| rs568340234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136079230 | CAGGGTGGGAACTGC[A/G]CTCTCTGAGCTGAGG | 138151 |
| rs568413268 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136086558 | CCACGGTCCCACCCC[A/G]GGCTCCACTGTGACC | 138151 |
| rs568420369 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136020560 | GGGTAGGAGGGAGAC[A/G]GGGAGGCCTACTCCC | 138151 |
| rs568436710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136075242 | CAGGGAGGTGGCCAG[A/G]ACTCCAGGACACATT | 138151 |
| rs568450671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136065806 | GGTGACAGAGACCCT[A/G]TCTCCAAAAAAAAAA | 138151 |
| rs568462120 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012832 | GATGGACCGGGCTCC[C/G]CCCCCACACGCCCAA | 138151 |
| rs568464997 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136092873 | GTCCAACTGGATCTC[A/G]GAACCCACTGCGTGA | 138151 |
| rs568465541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136025948 | CAACAACTAACAATA[C/T]GAACTCAAAAGAATT | 138151 |
| rs568476894 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136035296 | AAAGGAACATCACCA[A/G]TATTGAGCCAAAGTG | 138151 |
| rs568490290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136078832 | CCCTCCAGGAACTGA[A/G]GCTCTCAGGGCAGGG | 138151 |
| rs568507272 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136083556 | GGCAGGTCCAGAGGT[A/G]TCTTCTGAGAAGGGA | 138151 |
| rs568525181 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136019989 | CAGAGGGTGGGTGCC[A/G]GGGCTGGGTGGGGGA | 138151 |
| rs568598857 | in-del | -/G | 0.00122075 | 0.0246756 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013637 | TCATTTTTCTGTTGT[-/G]GGGGGTTGCATCCAC | 138151 |
| rs568638020 | snp | A/G | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136095849 | AAAGACGAGGATACG[A/G]GAGCGCCCTTGGGCG | 138151 |
| rs568649529 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136075523 | GTTTCTCAAACAGAT[A/C]GCGCAGCTGGGGCCA | 138151 |
| rs568653851 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136093195 | CTGCCCACAAACCAG[C/G]AAAGCAGGACTCCGG | 138151 |
| rs568667696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136021033 | AATGGAAATGATTGA[C/T]GAGCTAGAATTCATC | 138151 |
| rs568691515 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015441 | GCCCAGGAGGCCACT[A/C]TCCCATGAGGACCGA | 138151 |
| rs568712555 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136072057 | AGCCTGGCCAACATG[G/T]TGAAACCCCGTCTGT | 138151 |
| rs568723780 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136028389 | TCCTTTTTTTTTTTT[G/T]TTTTTGAGACAGGGT | 138151 |
| rs568764514 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011415 | TTTCTCAGGCAACAG[G/T]AGCAGTTCAGTAGGT | 138151 |
| rs568810167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136080749 | CAGACACGTGGAGAC[A/G]GGGGGCCGTGACACA | 138151 |
| rs568921855 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136085400 | GATCCACACCTATAG[G/T]CCCAGCTACTCCAGA | 138151 |
| rs568923506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136022930 | CCGTGCCTGTTAAGA[C/T]ACAGCCCGTTTCGTG | 138151 |
| rs568935602 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136028833 | CTGCTCCGATTTTGG[A/G]GCAAAGTTGTAGCTG | 138151 |
| rs568939006 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136090805 | GGCCGGGCTGCCCTC[A/G]GGGCCCCGGTGGCTG | 138151 |
| rs568958762 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136077062 | GCGGGCGCCTGTAGT[C/T]CCAGCCACTTGGGAG | 138151 |
| rs568983343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136023614 | CAGGCCTCCGACAGG[A/G]ATCCCAGCGATGATT | 138151 |
| rs569055223 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136088468 | AGCTGCAAAGCCACA[C/G]TGGTCAGTCAGCAGG | 138151 |
| rs569085607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136082592 | AGGTAGAGCCGAGGC[A/G]TCTTAGCAGGTGCTG | 138151 |
| rs569096424 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136017678 | ACTCCTCACACCCCA[C/G]CCTGGTAGGCTGCCA | 138151 |
| rs569101856 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136068154 | ATATGCTACTAAAGA[C/T]TGTATAAACACCGAA | 138151 |
| rs569110694 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136073574 | TCAAAGTGAAATGCA[C/T]AATTGGTCTCGAATG | 138151 |
| rs569115432 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136086504 | AGGGACGTCGCATGC[C/G]CCCAGCTTCCCGACA | 138151 |
| rs569144048 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136087310 | ACCTGTGGGCTCTGT[C/T]GTGGTGGCCCCAGGA | 138151 |
| rs569209163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013056 | TTTTCTCCTCATCTT[C/T]CCCTCAATCAGACCA | 138151 |
| rs569245053 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008637 | GGGAAGGGTCCGGCT[A/T]TCTTAATTGGTTTCC | 138151 |
| rs569247456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136062989 | CATGGCCTGTGCTCA[A/G]CCCCATGCCTGTCTT | 138151 |
| rs569263444 | in-del | -/CCAAGATCGCA | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136067200 | GGACGTTGCGGTGAG[-/CCAAGATCGCA]CCAAGATCGCACCAA | 138151 |
| rs569323071 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136021175 | ATAAAGAAATCTCGA[C/T]ACTCAACAGTTAAAA | 138151 |
| rs569354698 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | NACC2 | GRCh38.p7 | 9:136042500 | GGAGACCTGGTGCTG[C/T]AATGACTGGACGTCC | 138151 |
| rs569396642 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136055174 | CATACCCAGCAACCT[A/G]CCGATGGGTGAGAGG | 138151 |
| rs569417119 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136038037 | GAATCAATGCTAATA[A/C]AACATGAATGAATCT | 138151 |
| rs569434591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136088093 | AGGTCAGCAGTATTC[A/G]GGGACTGTCGGGCTT | 138151 |
| rs569441347 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136029922 | CCTGCTGGGCCGAAC[A/G]GGTGGAATGAGCCCA | 138151 |
| rs569441876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136024758 | CAATATTAGACTAAC[C/T]CCCTCATCAAAAACA | 138151 |
| rs569471856 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136082114 | ACACGACCTGCCGGG[A/G]CCCTGGGTCAGCTCA | 138151 |
| rs569493597 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136018696 | CCACTACAGGGGTCA[C/G]GCAGCATTTCCCGGT | 138151 |
| rs569544929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136073585 | TGCACAATTGGTCTC[A/G]AATGCCAAAGAGAAC | 138151 |
| rs569563668 | in-del | -/GT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024092 | TGAGTGAGGGCCAGA[-/GT]GTGTGTGTGTGTGTG | 138151 |
| rs569564781 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010989 | GGTGGAAGGCCCGGT[A/G]GGCCTGGCCCCGAGT | 138151 |
| rs569568523 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136065300 | GACCAGCCTCGGCAA[C/T]ATAGTGGGACCTCGT | 138151 |
| rs569575444 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136030245 | CAGGCTGTACAAAAA[C/T]AGGACACGGGACAGA | 138151 |
| rs569590568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136065755 | AGGCTGCAGGAAGGG[A/G]CTGGAGCCGTGATCA | 138151 |
| rs569639575 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136062167 | CAGGACAGGACAGGA[A/C]AGGACAGGAAAGGAA | 138151 |
| rs569650785 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007682 | GAGCTCTGGATTCTG[C/T]GCTTAGGACTCGCTG | 138151 |
| rs569661152 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136093184 | GGGAGACCACACTGC[C/T]CACAAACCAGGAAAG | 138151 |
| rs569696328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136083597 | ACCTGTGAAGAGCGC[C/T]GTGCAGAGGCCAGGC | 138151 |
| rs569710881 | in-del | -/TT | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136097225 | TTTTTTTTTTTTTTT[-/TT]GAGTCCGAGTCTCAC | 138151 |
| rs569737776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136079792 | CGAAATCTTGAAGCC[C/T]GTAAGATTTCAGGCC | 138151 |
| rs569744030 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136055305 | CCGGCAGGATTCACA[C/T]AAGGACACAGGTTAC | 138151 |
| rs569759545 | snp | A/G | 0.00438332 | 0.0466095 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011263 | AAGCTACACTTGGAG[A/G]CTGACCTTGTGAATA | 138151 |
| rs569775476 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136060822 | CTCCCCTGCTCATCC[C/G]TCCCACCAGACATGG | 138151 |
| rs569806719 | snp | C/G | 0.193966 | 0.243639 | intron-variant | NACC2 | GRCh38.p7 | 9:136049137 | AAAGAAAGGAACGGA[C/G]AGGAGGGGGAGCGAC | 138151 |
| rs569814052 | snp | C/T | 0.000117021 | 0.00764831 | missense | NACC2 | GRCh38.p7 | 9:136011842 | GCGGGAACTCGGGGT[C/T]GAGGGGCACGCTGGC | 138151 |
| rs569850888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016570 | TGAGGCCACTCTGTG[C/T]CGCTCTCCTGCTGGC | 138151 |
| rs569905114 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136080235 | CACCCCCAGCCTGTA[A/C/T]AGCCTCATCCCAGCA | 138151 |
| rs569921606 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136027173 | GAGGTTGCAGTGAGC[C/T]GAGATAGCGCCACTG | 138151 |
| rs569926438 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012324 | TCTCTCCGGGCTTCC[A/G]TAGCCCCAACGGCTA | 138151 |
| rs569931330 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136075631 | CCTGCGGGAGCAGAG[A/C]CTGCAGGGCCCCCTC | 138151 |
| rs569968396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136032270 | ACGAAGTTATTTCAA[C/T]ATTTGGAAAAGCAGT | 138151 |
| rs569990452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136033074 | CCAGCTACTTGGGAG[A/G]CTGAGGTAGGAGAAT | 138151 |
| rs570042493 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136093485 | CGGGTGGCTCCTCCC[C/T]GCCTTCCCGCCAGGC | 138151 |
| rs570057215 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136056398 | GTGTGCTCACCTCCC[C/T]GCTACTGGACATACA | 138151 |
| rs570058229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136021664 | CAGGAACGCTTATCC[C/T]GTCTCTACTCTTGAA | 138151 |
| rs570077135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136066489 | ATGGCTATAATCAAA[A/G]AGACAGAAAACAAAG | 138151 |
| rs570077588 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136075618 | CGGGGTCGCAGGTCC[C/T]GCGGGAGCAGAGCCT | 138151 |
| rs570079616 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136093015 | TCTGCCCCACTGACG[C/G]TGGCTGGGGCCACTG | 138151 |
| rs570088083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136024126 | GAGGACAGAGGGTGC[A/G]TGTGAGGACAGTGTG | 138151 |
| rs570089903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136018067 | TCAGCTGTGCAGAGG[A/G]AGGGGTGGGGTGGAA | 138151 |
| rs570163688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136019066 | TGCCTTGCCGTGCAC[C/T]GGGTGCTGCTGGCTA | 138151 |
| rs570165241 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007464 | ACACGCGCACACAGA[C/T]GCACACACACAGACG | 138151 |
| rs570190451 | snp | C/G/T | 0.00199529 | 0.0315338 | intron-variant | NACC2 | GRCh38.p7 | 9:136071371 | AACATGGTGAAACCC[C/G/T]GTCTCTACTAAAGAT | 138151 |
| rs570203611 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007724 | AGACAGAGGGTTCTT[A/G]GAGTTTTCAGTTGGT | 138151 |
| rs570251472 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136018500 | TGAAACCACCCACCC[G/T]GGAGTCACCCTGACA | 138151 |
| rs570390137 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136059445 | GCGCTCCTGAGAAAG[G/T]GGACAGCGGCAGCCC | 138151 |
| rs570391787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136043649 | GAAGCAAAAGGGCAG[C/T]AGGAGGCAGCAGGGT | 138151 |
| rs570417419 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136076563 | GGGAGTTGGTGTTCA[A/G]TGGGTGCAGTTTCGG | 138151 |
| rs570454089 | in-del | -/CT | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136085498 | GGCGACAGAGCAAGA[-/CT]CTCAAAAAAAAAAAA | 138151 |
| rs570466984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136072622 | TTTGGGATGCCGAGG[C/T]GGGCGGATCACCTGA | 138151 |
| rs570467013 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136077761 | GAGCAGGCAAGGGGG[C/T]AACAAAATTGTGCTT | 138151 |
| rs570478104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136046439 | CGGCCACAGGGCCAG[A/G]AGGAAGGTCCCTGCC | 138151 |
| rs570643010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136063396 | CAATCCAGGAAAGAG[A/G]TCACGTACATTGCAG | 138151 |
| rs570694565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136091312 | TACTCTGTAGCAGGA[C/T]GGCCTCAGGGAGGAC | 138151 |
| rs570696428 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096809 | GATCTCTCAGTGAGC[A/G]TAGCTACCCCAAGCC | 138151 |
| rs570720763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136092042 | CGAGATCCACCTGGG[A/G]ATTAGGGGGCGCCTC | 138151 |
| rs570741598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136083092 | GAACCTTTCTGGCAC[C/T]GCAACAGAAACCTGA | 138151 |
| rs570838297 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136069756 | CATAATAATTAAAGC[A/G]TCAATCCACTAAGAC | 138151 |
| rs570858050 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136030756 | AACCTGCGCCTCCCA[A/G]GTTCAAGCGATCCTC | 138151 |
| rs570904897 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136017222 | CCTGCATCCTCAGGA[C/T]CTGCAGCTGTGCAGC | 138151 |
| rs570907872 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136087552 | GGGGAAGGGCCCCGC[A/G]GCTTCTGGGGCCGCC | 138151 |
| rs570909572 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136059504 | AAACCCCACCCGGGC[A/C]GCCTCCTTGGGTGTG | 138151 |
| rs570924087 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136024854 | GCCAGCCCTGGGGTG[A/G]AGCAGCTGAGGCGGC | 138151 |
| rs570925140 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136090204 | ATGGGCACAGCCCCC[A/G]AGGCAGATGCCCAGG | 138151 |
| rs570933268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136056011 | CTTGCCCACCTCCGC[A/G]CAACGCCTTCCCTTT | 138151 |
| rs570979972 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136080718 | AGTGTGGGTTAGCTG[G/T]GGGTCTCCTCCTCTC | 138151 |
| rs570997332 | snp | C/T | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012347 | AACGGCTAACGGGAA[C/T]TGGTCAGAGGGTCCC | 138151 |
| rs570999548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136025797 | GTATGCACTTGTAGT[C/T]CCGGCTACTCAGGAA | 138151 |
| rs571013902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136069186 | GCTGGGATCATAGGC[A/G]TGAACTGCCGTGCCC | 138151 |
| rs571034119 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136079113 | CACGTAACCTGAAAT[C/G]TACTCACGTATGTCT | 138151 |
| rs571068937 | snp | A/C | | | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015720 | CACCAAAGAAGATGC[A/C]CATGGCGTGGGTCAG | 138151 |
| rs571076272 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136032541 | GTAAGAAGTTCTGGC[A/C]AGTTCAATGAGGCAA | 138151 |
| rs571080885 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136019727 | CCTGGACCACACGGG[C/G]CGAAGCAAACACAAG | 138151 |
| rs571153538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136064685 | TCTCTATCAAAATTC[C/T]GGTTAATTTCTTTGC | 138151 |
| rs571243485 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024578 | GGACAGAGTGTGTGT[G/T]TAAGGACAGAGTGTG | 138151 |
| rs571248457 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136026966 | GGGTGCAGTAGCTCA[C/T]GCCTGTAATCCCAGC | 138151 |
| rs571267015 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136089440 | GACTTCAGAGAACTC[A/G]AGGCCCTTCAGGTTC | 138151 |
| rs571305074 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136028173 | GGCTGAGTGGCAGGA[C/G]CCACTCCAGCCTGAG | 138151 |
| rs571346693 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136071483 | GGGAGGTGGAGGTTG[C/T]ACTGAGCTGAAACCA | 138151 |
| rs571365237 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136090751 | GAGGCTGATGCTCTA[C/T]CCCTTCACAGACTAC | 138151 |
| rs571367034 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136063855 | ACCACCTGCACCCCA[A/G]CCTGGGAAACAGAGC | 138151 |
| rs571403929 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012383 | CGGGAATAACACACC[A/C]CTCCCCGTCCCAGTC | 138151 |
| rs571426730 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NACC2 | GRCh38.p7 | 9:136094789 | CCGGCTTCCCCACCC[C/G]GAGGGCTGGATCGGC | 138151 |
| rs571431013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136090302 | ACTTCCTTCTGCTCC[A/G]ATCCAAAGGCAGGGC | 138151 |
| rs571518930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136017645 | GTGCTCACATGCCAC[A/G]GTGGACACCAGTCCG | 138151 |
| rs571534890 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136033482 | AACCCCTACTAAACC[C/T]CTACTAAAAATACAA | 138151 |
| rs571547831 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136071979 | ACGGTGGCTCGAGTC[C/T]GTAATCCCAGCACTT | 138151 |
| rs571575110 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136022857 | CACCAATTTAATCAT[G/T]CCACGCCATAACTGG | 138151 |
| rs571589537 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136084060 | AGCCTGAGGAAGAGC[A/G]GGGAGGTAGGGAAGG | 138151 |
| rs571621136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136062618 | AGCCTCATTTATCAC[C/T]CTAAAAATTATACAG | 138151 |
| rs571627492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136035563 | GGATTAAATACCACA[C/T]CAGGGAAAAAACCAC | 138151 |
| rs571630005 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012925 | TAAGGGGTTTTGTTC[A/C]AAAAGGAAAATTAGA | 138151 |
| rs571630821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136069233 | CTTTTAGATAGCATA[C/T]AGCTGAGTCATATTT | 138151 |
| rs571643747 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008445 | ATAACGTAGCTCTGT[A/G]ATAGATTCTATATAG | 138151 |
| rs571797034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136081493 | CGGTGCCGGGCGTCC[A/G]CTTCCACCTCGGGCT | 138151 |
| rs571800819 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136021191 | ACTCAACAGTTAAAA[A/C]CCAACAATCCAGTTC | 138151 |
| rs571824150 | in-del | -/CGG | 0.00597247 | 0.0543191 | intron-variant | NACC2 | GRCh38.p7 | 9:136056323 | CTGGGCCAGGGCCCT[-/CGG]CGGCCAGGAACTCCC | 138151 |
| rs571836305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136029881 | AGAGGTGTGGGATCC[A/G]GGCCGGTAGTGCAAA | 138151 |
| rs571870270 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031963 | CAGCTTTCCCGATGC[C/T]AGGGCCTGGTGCTCT | 138151 |
| rs571891857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136057590 | CGTAAGCTTGAAGAG[C/T]GTCTCCCTCGGGCAT | 138151 |
| rs571974144 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136020081 | GCCGATGGCAGTGAT[C/G]CTCACAAAACAGTGG | 138151 |
| rs571978870 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136091769 | CCCAGCCAGCCAGGA[C/G]GCATATTTTACAAAT | 138151 |
| rs572005555 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NACC2 | GRCh38.p7 | 9:136043107 | CAAAAAGCACTAGCC[A/G]TAAAATACAACTTTA | 138151 |
| rs572010825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136019414 | CTGAGCCTGGGTCTC[A/G]GGTACTGGGGGACCC | 138151 |
| rs572040172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136086724 | CCGACCAGTGGCCCC[A/G]TTTCCCTCCCACGAC | 138151 |
| rs572057640 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136025440 | CCAAATGATAAAAAA[A/C]AAAACAAAACAAAAC | 138151 |
| rs572080529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136058453 | GGAGGCTCCCCAGGG[C/T]CCTGGCCATCCATAT | 138151 |
| rs572166065 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136030980 | CATCTCAACTTTAGA[C/T]GGAGCCGATGAACTT | 138151 |
| rs572186463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136074594 | ACAGACGGACAGGTC[A/G]AAACCATTCCTCGTT | 138151 |
| rs572234706 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | NACC2 | GRCh38.p7 | 9:136059926 | GATGTCCTGACCAGC[A/G]GAGAGGGGCCGCACC | 138151 |
| rs572312571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136078389 | CTGGCTCTCTCATTT[C/T]AGGAACTAAAGGCCC | 138151 |
| rs572313044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136083270 | CCAGGTACAGTCAAT[A/G]CTTCACCCCAACCTG | 138151 |
| rs572321460 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136060525 | CCCCTCCCTGAGGGT[C/G]AGCTCCACACTGGGG | 138151 |
| rs572326278 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015256 | AGCACCAGGGCCCGC[A/G]TGGGCACCTGCGCCC | 138151 |
| rs572363308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136079519 | AGCCCCTCCTCACCC[A/G]CAGGCATGGGCACCC | 138151 |
| rs572455250 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011065 | CCTGCCCCGTCGCCC[C/G]AGAGAGGTTCCATGG | 138151 |
| rs572485169 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010750 | TCCCACAGTGGGCCC[A/G]GGCGGGACAGTGGGA | 138151 |
| rs572550786 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | NACC2 | GRCh38.p7 | 9:136051021 | GGAGGGGCCGCGCTG[A/G]AGCAGCGGGGAAGGA | 138151 |
| rs572572585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067401 | TAAAATTCACGATGG[C/T]AATGGTTGCATAACT | 138151 |
| rs572582163 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136027629 | AACACAAGGGCAAAA[-/G]GGGAAAAAAAAATCA | 138151 |
| rs572584271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136092522 | GCTTTGCTTCTCCTT[C/T]GAGCCACGCCTGGAA | 138151 |
| rs572585054 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136088263 | CTGGGAACTGTACCA[A/C]TGCCCACATCAGGCC | 138151 |
| rs572643439 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136027473 | ATATACAGGGGCTCA[C/G]GGAAAGTCTCAACAA | 138151 |
| rs572671839 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136083672 | GCTGGCACCACGCTG[A/C]GGAGGCAGGCGGGGG | 138151 |
| rs572685866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136031819 | TAGTGGCCACTCATG[A/G]AACCGATTTAACCCA | 138151 |
| rs572733329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136055578 | TCTAAGCCCAGCACA[A/G]CAAACCAGAGGAATG | 138151 |
| rs572894695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136017728 | GTGAGGGCGGAGCAC[C/T]GCCTCCCTCATTCCT | 138151 |
| rs572898910 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067514 | GCAGGTGATTTTGTC[A/G]TTCTGTGAACACCAC | 138151 |
| rs572907892 | in-del | -/AC | 0.0015984 | 0.0282249 | intron-variant | NACC2 | GRCh38.p7 | 9:136042662 | CACACACACACAGAA[-/AC]ACACACAGACACACA | 138151 |
| rs572959041 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136077857 | ATGAATACTGACTTG[G/T]GCTTTATACGCAAAG | 138151 |
| rs572970575 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136094607 | GCCGGACCCCAGTTT[A/C]TCCCCAGGCTGGGGC | 138151 |
| rs572988925 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010636 | AACCATATATGAAAT[A/G]GATCTAAATTACAAC | 138151 |
| rs573012237 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136086103 | CTCCAGGCCCTTCAC[C/T]TCGGGCTGGAGAAAA | 138151 |
| rs573015103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012584 | TCGGCTGCCACCCCA[C/T]ACTTGGGGACTGTAA | 138151 |
| rs573028033 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136090351 | AGACCGCCGCAGAAG[A/C]ACCAAGGAAGGCCCA | 138151 |
| rs573041243 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | NACC2 | GRCh38.p7 | 9:136020463 | GACCACGCAGGCAGC[C/G]CCACCAGGGGAGTCT | 138151 |
| rs573052153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136087647 | TACGGTACCCCATTC[A/G]GAGCTCACAGCGGGA | 138151 |
| rs573090540 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008229 | GGCACCCAGCCAGGC[A/G]CGGCCCGCCGGGCTC | 138151 |
| rs573092114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136057690 | GGTCTCCCCTGCACC[A/G]GCTCGGCCGGGTGGA | 138151 |
| rs573109620 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NACC2 | GRCh38.p7 | 9:136075013 | CAATCGGATCCTCAC[A/G]AAACAGTGACGTGAG | 138151 |
| rs573111411 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136085670 | CCACACTGGAACAAG[A/T]CACACAGGTATGCAG | 138151 |
| rs573129654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136035866 | GATACAGAAGTTCTC[C/T]GTACTTATCTTACAA | 138151 |
| rs573156054 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009583 | GCTGGGCCTGGCTGG[A/C]GGCAGCCCAGGAGGC | 138151 |
| rs573196231 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136097107 | ACCTTTTAAAGCAAA[C/T]CCTGCATCCCTACTG | 138151 |
| rs573329822 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136083629 | GAGACTGGCACGAGA[C/T]GGGCATGAGCCCAGG | 138151 |
| rs573335471 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136018783 | AAAACAACCCGGGTG[G/T]TATTTTAAAACATAA | 138151 |
| rs573359615 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136024207 | TGTGTGTGAGGACAG[A/T]GTGTGTGTGTGTGAG | 138151 |
| rs573364993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013658 | TTGCATCCACAAGCC[C/T]GTTTGAGAAAGGCCA | 138151 |
| rs573402507 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136073660 | ATGTTTGCAGAAAGT[C/T]GACTTGATTTCCCTC | 138151 |
| rs573430146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067703 | AGCCGAGCGTGGTGG[C/T]GGGCACCTGTAGTCC | 138151 |
| rs573443705 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136091974 | CACAGCCAAGGCCCA[A/G]ACAACCTTCCAGTCA | 138151 |
| rs573602442 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136050731 | CCTGGCTGGGACACT[A/C]CAGAGAAGGGACACG | 138151 |
| rs573716696 | snp | C/T | 0.000399281 | 0.0141238 | missense, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136011971 | TGCACATGTCCGCGG[C/T]GATCACGTTCATCTC | 138151 |
| rs573749546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136021375 | CCGACGCCAAGTGCC[A/G]GCGAGGATGCGGGGC | 138151 |
| rs573762851 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136026869 | GAGACCAATGGACAA[A/G]ACGGTAGATTAACCC | 138151 |
| rs573825044 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136026172 | TGGCAAAACTCCGTC[G/T]CTACTAAAAATACAA | 138151 |
| rs573825544 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136075666 | AACCTGTGCTGATGC[C/T]GTCCTGAGCTCCCTG | 138151 |
| rs573830218 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007510 | ACACACATGCACAGA[C/T]GCGCACACACAGACG | 138151 |
| rs573849894 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136093273 | AAGATCGTCACTGTT[A/G]TTTCATGAATAATGC | 138151 |
| rs573863648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136070455 | GAGGTTGCAGTGAGC[C/T]GAGATCGCGCCACTG | 138151 |
| rs573876012 | in-del | -/GACAGGACAG | 0.49655 | 0.04139 | intron-variant | NACC2 | GRCh38.p7 | 9:136062115 | TGGGCAACAGAGCGA[-/GACAGGACAG]GACAGGACAGGACAG | 138151 |
| rs573916590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136032477 | AAACATCCTACTTAA[A/G]GAGGAACAGTGGAAG | 138151 |
| rs573921455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136016043 | TGCAGCCCCTGCCAA[C/T]CAGGAATGCGACCAG | 138151 |
| rs573928562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136070055 | ATATTCTGGGCCAGA[A/G]AGAAAACTTCAAGAA | 138151 |
| rs573944070 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136093601 | CTCTCTGTGCCCATT[C/G]CAAGTGGCTTTGCCG | 138151 |
| rs573950641 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NACC2 | GRCh38.p7 | 9:136055729 | AGCAAATGCACAGCC[A/G]TTAAACACGTGGTAG | 138151 |
| rs573978086 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136061658 | CCTCAGCCCTCACAC[A/G]GCCAGGTGGCAACAT | 138151 |
| rs574107002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136033365 | AAATGAACTTCTGGC[C/T]GGGCACGGTGGCTCA | 138151 |
| rs574174229 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136084662 | AGCGGCAGCACCAGA[C/G]AGCCAAGAGGCAAGT | 138151 |
| rs574231341 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136076651 | TTCTTACTGCCACTG[A/T]ACTGTGCGCTTAAAA | 138151 |
| rs574247062 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NACC2 | GRCh38.p7 | 9:136043774 | CAACATTGCACTTGA[C/T]TGCACAGTGAACTCA | 138151 |
| rs574250968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136030049 | CTGCTTAATTTTCGT[A/G]ATTTTAGTAGACATG | 138151 |
| rs574257907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136022377 | CAACACCCTCCTGCC[C/T]GATGCCCAGCAAGGC | 138151 |
| rs574298273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136021935 | TGTGGCCACCAGGGG[C/T]TGGGGTGCGGACAAG | 138151 |
| rs574313717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136042791 | AGACACACACACACA[C/T]AGACACAGTGTTGCC | 138151 |
| rs574343502 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136091001 | CGGCCGCCCATGGCC[A/C]TGTGCCCTCCTGGAT | 138151 |
| rs574348505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136063478 | GTTTGACCTGTGGCC[A/G]AGCCTGCAAGTTCTC | 138151 |
| rs574429348 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136087399 | CTCCTGGCCTGTCAC[C/G]TGCACAGCTGCAAAT | 138151 |
| rs574434801 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136030351 | GCGGTGGCTCACGCC[G/T]GTAATCCCAGCACTT | 138151 |
| rs574482086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136058368 | AGGCCCTTCCCAGCC[A/G]GGGACCCGGGATTCC | 138151 |
| rs574495330 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067904 | TATGGCATAGCCTAG[A/T]GCTCCTGGGCTATAA | 138151 |
| rs574516399 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136085284 | CCTCCTGTGTAGCTG[C/G]GATTACAGGTGTGAA | 138151 |
| rs574526561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136063260 | GCAGAGCACCTGGGA[A/G]CAACGCACCAGCGAG | 138151 |
| rs574567063 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136064215 | AATCACTTGAGCCCA[A/G]GCGATCGAGGCTGCA | 138151 |
| rs574576998 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136086704 | GACTCCTAGGAAAAC[C/T]CTCCCCGACCAGTGG | 138151 |
| rs574604711 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136078335 | TGCAGAATTCATGAG[A/G]GGGACAGGCACATCT | 138151 |
| rs574698544 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136077956 | TGTACTTCTTTTTAG[A/T]AGAGACGGGGTTTCA | 138151 |
| rs574703409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136064735 | CTAAAAATTCATATG[A/G]AAACGCAAGGGACCC | 138151 |
| rs574712700 | snp | A/G | | | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015930 | TGGAACCTGGCCGTT[A/G]CCCTCAAAGGCTGCA | 138151 |
| rs574720495 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NACC2 | GRCh38.p7 | 9:136024505 | GTGTGAGGACAGAAT[A/G]TGTGTGTGTGTGTGT | 138151 |
| rs574724106 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136019318 | GAGTCGGGGCCAGAG[C/T]TGGGTTCCAGGGTGG | 138151 |
| rs574776231 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136055601 | GAGGAATGCGGCACT[A/G]AATTTCTGCAGGATC | 138151 |
| rs574785082 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NACC2 | GRCh38.p7 | 9:136088176 | CTGTGCAGGGTCAGC[A/G]GAATTTTGCTCTAAA | 138151 |
| rs574787724 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136074467 | CAAAAAAAAAAAGAA[A/T]AAAGAAGAAAAAGAA | 138151 |
| rs574795305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136087858 | CGGTCTGAGCTGCTC[A/G]AGGGAGGGCAAGCCC | 138151 |
| rs574799066 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136082776 | CGGGTGGGGCTGGCT[C/G]TTGGCCAGCGGATCC | 138151 |
| rs574902423 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136092427 | ACATGCATCAGACGG[C/T]GGCTCAGGTCCAGCG | 138151 |
| rs574917630 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136097269 | GCTGGGGTGCAGTGG[C/T]GCGATCTCAGCTCAC | 138151 |
| rs574942998 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015170 | CCATCAGCCCCACAC[C/G]CCAAACAGAGGCCAC | 138151 |
| rs574944889 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010294 | CCTCAGGCACCCTCC[A/G]TCCATGCACACCCCT | 138151 |
| rs575072228 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006048 | CCGCGGGCCCAGCTC[C/T]GCCCACCTGCACTTG | 138151 |
| rs575082554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136092787 | CCGGAGAAACATGCT[A/G]GTGTATCCTGGGGTA | 138151 |
| rs575142870 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136021818 | GGATGGATCTCAAAT[C/T]GTGCTGTTACACAGA | 138151 |
| rs575181326 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136089810 | AAAAAAATCCAATTA[C/T]AGCACAAATCTCTCA | 138151 |
| rs575206290 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NACC2 | GRCh38.p7 | 9:136026880 | ACAAGACGGTAGATT[A/G]ACCCAGCAAAGTCAG | 138151 |
| rs575247993 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136091704 | AGGCCACAGCTGAGG[G/T]AGCTAGGGCTCCCAG | 138151 |
| rs575248397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136022321 | ACCACACTCTCCACA[C/T]GGGGCTGTGTCCCAC | 138151 |
| rs575294031 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136020576 | GGGAGGCCTACTCCC[C/T]AAAAGTGTATACCAT | 138151 |
| rs575358857 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136093989 | GTGGGTGAGAAGAAG[A/G]GGCGACCTGGAGGGA | 138151 |
| rs575369429 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012127 | TGAGCCTCCCCGGCC[A/G]CTCCTGGGGCCCATG | 138151 |
| rs575371449 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136017310 | CAGCCCATGGTGCCA[A/C]CCCGAGGTCCCTGGG | 138151 |
| rs575387300 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136062109 | CCAGCCTGGGCAACA[A/G]AGCGAGACAGGACAG | 138151 |
| rs575414821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136017830 | TCCCACTGCCCTGGG[C/T]TCCTGCACACCCTAC | 138151 |
| rs575450097 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008167 | GACGACAGAGAACTC[G/T]GGTGGACAGACACAA | 138151 |
| rs575457874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136016707 | GAGGCGAGAGATGCC[C/T]GCTCAGGCCCAGGGA | 138151 |
| rs575556861 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NACC2 | GRCh38.p7 | 9:136016993 | AGGGGCAGTGGGGCA[C/T]GGCCACCTGACTCAG | 138151 |
| rs575566069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136057181 | CCTGTGTGACTGAGC[C/T]GAGCCCTGCGCTTAT | 138151 |
| rs575600539 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136081571 | CACAGCTGCCGAATC[G/T]CTGCAAAGGCCTCTC | 138151 |
| rs575638759 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | NACC2 | GRCh38.p7 | 9:136056704 | ATCACTGTCGCCCCA[G/T]CCTGGGAGGTGGAGG | 138151 |
| rs575663498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136035633 | CAGTCTGTAGTTACA[C/T]GAGGATGATGGATTG | 138151 |
| rs575668343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136087823 | GATCCCCAACGAGGC[C/T]CCAAGCGCCCTGTCC | 138151 |
| rs575707495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136081174 | CCTCAGTGGCCACTC[A/G]GGGACTCTCCAGCCA | 138151 |
| rs575715203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136023847 | TGTGCTGAGAAGGAC[A/G]ACCAGGACACTAAGG | 138151 |
| rs575726043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136033624 | ACTGCACTCCAGCCC[A/G]GGGGACAGAGCAAGA | 138151 |
| rs575726927 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136058074 | CATGTAAATCAGAGC[C/G]ACACAGAAACACTAC | 138151 |
| rs575787095 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136029540 | GCCCCTTGCCCACCA[C/T]GTTGTGGGCAATGAG | 138151 |
| rs575850631 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136028966 | TCGAGCACAAGAGGG[A/T]GGCCGAGGTGGGGCT | 138151 |
| rs575874144 | snp | C/G | 0.0310518 | 0.120672 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136095606 | CGCGGCGCAGAGGAC[C/G]GAGCTCGGCGGCCGG | 138151 |
| rs575883573 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136080099 | AGTCCCTACCCCGGG[C/T]GTGGCTGCCAGCCAA | 138151 |
| rs575893083 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136072892 | AAAATGAATTGGAGA[C/G]TTAAACATAAAACTA | 138151 |
| rs575894057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136018100 | TGCACGTCCAGCAGG[C/T]TCGGGGCAGGCAGCT | 138151 |
| rs575957211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136072267 | AAAAAACCCAAAGGC[A/G]GGGCATGGTGGCTCA | 138151 |
| rs575977327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136020675 | CAAATGGACAGAACA[A/G]TGCTGAATCAACTGA | 138151 |
| rs575977427 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015274 | GGCACCTGCGCCCCA[C/G]AGCCCAACCCCAGGG | 138151 |
| rs576013086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136082955 | CTCACTCCTGCCAGA[C/T]ATCAGGGCGAGGGGG | 138151 |
| rs576017463 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136078972 | GGCATGATGCCGCGC[C/T]GCCGCCGCCCCTCTC | 138151 |
| rs576033133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136025505 | CAGATCAGACAACTA[A/G]CAGACACCGAATTTA | 138151 |
| rs576052719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015940 | CCGTTACCCTCAAAG[A/G]CTGCAACTGGACCCT | 138151 |
| rs576058429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136046958 | TTAACGCGAGAGAGG[A/G]TGGAACAGGCACACG | 138151 |
| rs576158139 | snp | A/C | 0.0554779 | 0.157039 | intron-variant | NACC2 | GRCh38.p7 | 9:136051052 | GGGAGGGAGGGGGGT[A/C]TCTGGAGCTGTGCAG | 138151 |
| rs576184868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136056105 | GGGAGGACAAGGGGG[C/T]GGCAGGGGGCCCGGA | 138151 |
| rs576236544 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | NACC2 | GRCh38.p7 | 9:136079360 | TCCTCTGGCTTCCAG[G/T]CAGGAGACACTCCTA | 138151 |
| rs576247805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136055640 | CAAGGGGAAGGGAGG[C/T]GAGAAAAATTAAATT | 138151 |
| rs576280295 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136075343 | GAAAGCCCTCCCTAG[C/T]TCCCCCGAGGCTGGC | 138151 |
| rs576315604 | in-del | -/T | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012673 | TTTTTTTTTTTTTTT[-/T]CTTTTTTTTAGGAAG | 138151 |
| rs576342600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136074950 | TCCTTCTGGGAGCCC[A/G]GGAGCTCTGTCCCCC | 138151 |
| rs576382652 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011145 | CCACCGCCGGCCCCT[A/G]CTTCGTCTTCCGGGC | 138151 |
| rs576464663 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136097277 | GCAGTGGCGCGATCT[C/T]AGCTCACTGTAACCT | 138151 |
| rs576469606 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136092920 | GAGTGACCCCAAGGG[C/G]CTGTGAGATGCAGAG | 138151 |
| rs576505917 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074647 | CTTCCTCAAGGAACC[C/T]ATCTCTGGTTCAACA | 138151 |
| rs576508029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136070313 | GAGTTCAAGACCAGC[C/T]TGGCCAAGATGGTGA | 138151 |
| rs576517890 | snp | C/T | 0.000798403 | 0.0199641 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011669 | CACCTCCTGGATGAC[C/T]GAGCCAGCCCCGTCC | 138151 |
| rs576526278 | in-del | -/G | 0.00120749 | 0.0245415 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014928 | CCCTCTGGGAACAAT[-/G]GGGAGGGAATGCTTT | 138151 |
| rs576555263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136057359 | TCAGAGGAAGAGAAT[A/G]ACTCGAAGGGTGGGG | 138151 |
| rs576569254 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136072356 | TTTGAGATCAGAATG[A/G]CCAACACAGTGAAAT | 138151 |
| rs576569261 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136088890 | GCATCCTGGGGGAAG[A/G]TTTCCCGGAGGAGAC | 138151 |
| rs576586803 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NACC2 | GRCh38.p7 | 9:136084315 | TGTGTCCAGCCCTGT[C/T]CCCATGCACACCTGG | 138151 |
| rs576602053 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136088727 | TTGGTCTTTCCTGAC[A/C]CACTGCTTCATGCCT | 138151 |
| rs576612117 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136088347 | GGGACCCTCAGACCC[C/T]ACTCCCTGCCTCTCT | 138151 |
| rs576627261 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136080402 | TGGGGTATTAAAAAC[A/G]TCTCTATTAAAAATA | 138151 |
| rs576643146 | in-del | -/AC | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007377 | CACGCGTGCACACAT[-/AC]ACAGACACGCGTGCA | 138151 |
| rs576661957 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136075991 | TGTGACAAAACTCCG[A/C]GACACCCGCTTCTCA | 138151 |
| rs576677703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136080012 | GGCTGCCTGGGCCAG[A/G]CCTGGGGCTGACCTG | 138151 |
| rs576713519 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031638 | CCACTGTGCCCGGCC[C/G]ACGGCCCCATTTTAA | 138151 |
| rs576727205 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136073794 | AAAGGTGCTTATGCA[C/T]CCTCTACTGCCAAGT | 138151 |
| rs576737501 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136089126 | TCAGTTACGCGGTTA[C/T]GTTTGCAGCACTGCA | 138151 |
| rs576766538 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136062727 | CAAGACTAGCCTGGG[A/C]AACATGGCGAAACCC | 138151 |
| rs576767602 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136042749 | ACACACAGACACAGA[C/G]ACAGAGACACACACA | 138151 |
| rs576802624 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136063935 | AACAGCTGTGCCCTC[A/G]TCGGCTAGAAGATAC | 138151 |
| rs576804031 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136073738 | TGCTACAATTTTGGC[A/C]CAATTTGCTCAGTTT | 138151 |
| rs576817153 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008852 | TCGGCCTGGCCCGCC[C/T]GGGGCGCAGGGAGAG | 138151 |
| rs576818206 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136062782 | CTTAGCCAAGTGTGG[G/T]GGTGTGTGACTGTAG | 138151 |
| rs576822378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136084640 | CAGACGCGCACGCCA[C/T]GTCCATAGCGGCAGC | 138151 |
| rs576865710 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136077918 | TAATATCAGTCCAAT[C/T]ATAGTTTTGTTTTGG | 138151 |
| rs576879308 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136094666 | ACGACCCACGAACGG[C/G]CCCACCTGGACCGGG | 138151 |
| rs576890927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136074179 | GGCATGGCCAGGCGC[A/G]GTGGCTCATGCCTGT | 138151 |
| rs576895806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136063070 | CTAATTTTTGTTCTC[A/G]TTGTTGTTGTTGAGC | 138151 |
| rs576910863 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008265 | ATCTGTCACACCTCC[A/G]GTCCCTCCTGGACCT | 138151 |
| rs576964143 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136063078 | TGTTCTCGTTGTTGT[G/T]GTTGAGCCCTTTCAC | 138151 |
| rs577009572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136090986 | GGGCCCAGGAGCTCG[C/T]GGCCGCCCATGGCCC | 138151 |
| rs577024534 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136095392 | CCGGCCGCGCGCGCG[C/G]GCGCACTGGCAGCCA | 138151 |
| rs577024541 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NACC2 | GRCh38.p7 | 9:136090441 | ACCAGCCCACTGGGC[A/G]GAAGCCCCAGGACAG | 138151 |
| rs577037757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136030031 | CTGTGACACACACTG[C/T]ACCTGCTTAATTTTC | 138151 |
| rs577043350 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136023966 | ACAACCCCCCCCACA[A/C]ACACGTGCACATGCG | 138151 |
| rs577055570 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136018918 | CATCCACAACCACCT[C/T]GTCTCGAGATGTTTT | 138151 |
| rs577067372 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067209 | CGGTGAGCCAAGATC[A/G]CACCAAGATCGCACA | 138151 |
| rs577090381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136081755 | TCCCCACCAAGTGGC[A/G]GCAGCAGCTGGCCCC | 138151 |
| rs577107650 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136029739 | AGCCCTGCAGGGAGC[C/T]GGCGCCTGTGCCAGT | 138151 |
| rs577110442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136087311 | CCTGTGGGCTCTGTC[A/G]TGGTGGCCCCAGGAG | 138151 |
| rs577118198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136092286 | CAGACACTCACCGCC[A/G]GGGAGCCTGACCGGA | 138151 |
| rs577230954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136067997 | GTGTATCGAAACATA[A/G]TAAAGGTTCAGTAAA | 138151 |
| rs577244650 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096542 | CCTGGCTTGCCTTGT[A/G]TGGGGGTGAGTATGG | 138151 |
| rs577264430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136079908 | AGCCGCTAGCCCTGC[C/T]ACCTGTTCCCCAAGG | 138151 |
| rs577331500 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136097146 | GCCCGTGCTACTGAG[C/G/T]ATGTACACCTTACCG | 138151 |
| rs577355174 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136064082 | TCACTTGAGTCCAGG[A/C]GTTTGAGACAAGCCT | 138151 |
| rs577367046 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136068568 | TCACTAGGCAATAGA[A/C]TTTTTCAGCTCTATG | 138151 |
| rs577370593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136063605 | ATCTCTTAAAAAGGC[C/T]GAGCACGGTGGCTCA | 138151 |
| rs577373711 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014066 | GGGGGGGAGGTGGAG[A/G]GGGAGGAGGAGCTGG | 138151 |
| rs577373758 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136019284 | CGTGGCCCCCGGAAG[C/G]GCCATTCAGAGGCCC | 138151 |
| rs577389471 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136080524 | TTGTGTGCTGAGATC[A/G]TGCCACTGCACTCCA | 138151 |
| rs577391078 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009695 | CGCCCAGTGGGAATG[A/C]GTCTAACCCACACCC | 138151 |
| rs577403379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136092028 | GGCTGAAAGGGAAAC[A/G]AGATCCACCTGGGGA | 138151 |
| rs577418392 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010628 | AGTTTCCAAACCATA[C/T]ATGAAATAGATCTAA | 138151 |
| rs577462638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136018842 | GCTGTGATTACACAC[A/G]CGGAGAAGCCGCACG | 138151 |
| rs577465323 | snp | A/C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136060933 | CTGGGTACAGGGGTC[A/C/T]GGGGGAAGGTGAAAG | 138151 |
| rs577478787 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136062684 | TTTTGGGAGGTCAGC[C/G]GGGGTGGACTGCTTG | 138151 |
| rs577495131 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136069528 | ATTCCAGCCTGGGTG[-/A]AAAGAGTGAAACTCT | 138151 |
| rs577501723 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010204 | CAACATGATCCCTAA[A/C]CCTCTGTCCCCTACC | 138151 |
| rs577515186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136093950 | GAGGGAAGGAGGTCA[A/G]GAGCCTGCCAGACGA | 138151 |
| rs577528064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136093662 | AGCTCCTTTTATTTC[C/T]TCCCCTTGGACTCTG | 138151 |
| rs577536909 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014469 | CCACCATGCCCAGTT[A/C]ATTTTGATGAAGTCT | 138151 |
| rs577588598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136032023 | CTCGGCAGCACCCCT[A/G]GTGATCACTGCCCAG | 138151 |
| rs577623566 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136077037 | ATAAATAAAATAGCC[A/G]GGTGTGGTGGCGGGC | 138151 |
| rs577628425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136016061 | GGAATGCGACCAGCC[C/T]AGGGGATTCAATTAA | 138151 |
| rs577642163 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NACC2 | GRCh38.p7 | 9:136059241 | CACCCTCAGGGCTAA[A/G]GCCAAAGGTGCCCAG | 138151 |
| rs577643318 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136071156 | GAGAATCGCTTGAAC[A/C]TGGGAGGCAGACGTT | 138151 |
| rs577651394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136089594 | CTCCTCTGAGGCTCC[C/T]CCAACTCATGTACCT | 138151 |
| rs577674670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136026884 | GACGGTAGATTAACC[C/T]AGCAAAGTCAGTAAC | 138151 |
| rs577702019 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136055737 | CACAGCCATTAAACA[C/T]GTGGTAGAGGAAGGA | 138151 |
| rs577737690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136026268 | ATTGCTTGAACCCAG[C/T]GGGGGTGGAGGTTGC | 138151 |
| rs577743974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136016663 | TGCCCTCACAGGGAA[A/G]CTCTTGTGAACGAGT | 138151 |
| rs577768531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136066167 | CACTGCACTCTAGCC[C/T]GGGCAATAGAGTGAA | 138151 |
| rs577771323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136071151 | GGCAGGAGAATCGCT[C/T]GAACCTGGGAGGCAG | 138151 |
| rs577860068 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136089292 | CAAAGGAGGACCCAC[A/G]GGCCACGTCTTCCTG | 138151 |
| rs577861788 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NACC2 | GRCh38.p7 | 9:136021411 | GGACGTCCTGACGAC[A/G]TGGTCTCACCTCCCA | 138151 |
| rs577879219 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136017745 | CCTCCCTCATTCCTG[C/T]GTCCCAGCACAAAAG | 138151 |
| rs577909605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012065 | CAGCCACCTGCCTGC[C/T]GGGAGGCCCGCCCCT | 138151 |
| rs577911511 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136032530 | GACAGGGATATGTAA[A/G]AAGTTCTGGCCAGTT | 138151 |
| rs578021156 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136061716 | AGGTCTAGCAGGCTC[A/C]GGAACCAGCGAGAAG | 138151 |
| rs578028756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136023306 | GAGCTTGCTCCCGAC[A/G]CGAGGGGCCGGCATG | 138151 |
| rs578028815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136017376 | TAGAGCGTTCATGGA[A/G]GGCCAGGGCTGAGAC | 138151 |
| rs578065822 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NACC2 | GRCh38.p7 | 9:136085012 | GGTGCTGAGGGCAGC[A/G]CAAAAATGTGCATGC | 138151 |
| rs578079065 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136090208 | GCACAGCCCCCGAGG[C/T]AGATGCCCAGGGCCT | 138151 |
| rs578083028 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136062049 | CGCTTGAACTGGGGA[C/G]GTGGAGGTTGCAATG | 138151 |
| rs578093145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136071731 | TGATCAAGACTGTGT[A/G]GTATGGACAGAGGGA | 138151 |
| rs578111522 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | NACC2 | GRCh38.p7 | 9:136028266 | CCATTACACAACAGG[-/T]TCTACAGAACAGGGC | 138151 |
| rs578144965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NACC2 | GRCh38.p7 | 9:136081093 | GGGGAGAAGAAACGC[A/G]CGTTTCCCATATTTC | 138151 |
| rs745366824 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136018095 | GAACCTGCACGTCCA[C/G]CAGGCTCGGGGCAGG | 138151 |
| rs745377046 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136017404 | GACCCCTCATCTGAC[A/G]ACCACCTGCTGGACA | 138151 |
| rs745432587 | snp | C/T | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096027 | CTGCCCAAGGCCACG[C/T]TCCTGAGGACAGAGG | 138151 |
| rs745447465 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136083073 | CCGAGCACTTCACAC[C/G]GCAGAACCTTTCTGG | 138151 |
| rs745474326 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136077539 | CTTCAGCAAAGGGCG[C/T]GTGGTCAGAGTATGG | 138151 |
| rs745480538 | snp | A/G | 2.74865e-05 | 0.00370709 | synonymous-codon, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136011957 | GCGGCGGGCGTTGGT[A/G]CACATGTCCGCGGCG | 138151 |
| rs745557843 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136072913 | CATAAAACTAGAGGG[C/G]AAAGAAAAAAACACA | 138151 |
| rs745559057 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136061993 | AGCGTGGTGGTGTGC[A/C]CCTGTAATCCCAGCT | 138151 |
| rs745566491 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136016950 | CAGGTACTGTGGCCC[C/T]CAACTCTTCTCCCAG | 138151 |
| rs745585982 | in-del | -/ATGCACACACAG | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007546 | CGTGCACACACAGAC[-/ATGCACACACAG]ACGCACACACACACA | 138151 |
| rs745659864 | in-del | -/AACT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136058613 | AGGGCAAAGGCTGAA[-/AACT]AACCCACCGGGTACC | 138151 |
| rs745662854 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136022708 | GGGCCCATCAACTAC[A/C]AGTGCTGGCTGGGGC | 138151 |
| rs745743553 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078358 | GCACATCTGGGGGCA[A/G]GTTCTCCAAATAATT | 138151 |
| rs745771934 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136088295 | AGATGGAAGGGATGA[C/T]GGGGGCAGGGGACAC | 138151 |
| rs745785649 | snp | A/G | 8.73096e-05 | 0.0066066 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014009 | GCTCGTGGCCTTCCC[A/G]GGCCATAGGGTCCGA | 138151 |
| rs745793432 | snp | C/T | | | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006134 | GGAAAGAAGGAGCCA[C/T]GCACCTTTTGGGTGG | 138151 |
| rs745843180 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007188 | CGACTGATCGGAATA[C/T]GAGCCGGTCGTCCAG | 138151 |
| rs745861172 | snp | C/T | 8.04149e-05 | 0.00634043 | missense | NACC2 | GRCh38.p7 | 9:136011707 | CGCCGGCGTCGAAGG[C/T]GGGGTTGGCGGCGGC | 138151 |
| rs745873586 | snp | G/T | 6.65303e-05 | 0.00576721 | missense, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016300 | TCCCCGGGGTCCCCT[G/T]CCGAGTAGAGCTTGG | 138151 |
| rs745875455 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136089417 | CCAGGCGAAGGGTAG[A/G]GGGTACAGACTTCAG | 138151 |
| rs746031247 | in-del | -/GAGTGT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024154 | GTGTGTGTGGGGACA[-/GAGTGT]GTGTGTGTGTGTGTG | 138151 |
| rs746064200 | snp | A/G | | | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014390 | GCTCACTGTAGCCTC[A/G]ACCTCCCGGGCTCCA | 138151 |
| rs746067177 | snp | A/C | 8.65763e-05 | 0.0065788 | missense, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013199 | CCCCCAGGCTCTTAC[A/C]TTTCACAGCGTTCAG | 138151 |
| rs746084341 | in-del | -/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136065079 | TCAAAGACCTAAATG[-/T]TAAGAGCTAAAACTA | 138151 |
| rs746129217 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067617 | CAAGGCGGGCAGATC[-/A]ACGAGGTCAAGAGAT | 138151 |
| rs746129331 | snp | C/T | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013497 | GGCTGAGAAGATGAC[C/T]GGGTGATGGGGCTGC | 138151 |
| rs746159757 | snp | A/C/T | 3.39289e-05 | 0.00411868 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013309 | TTCCTGGTGGAGGGA[A/C/T]CGGAAAGGCAGGCAG | 138151 |
| rs746230039 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067488 | GGTGATTTTGTTGTT[C/T]TCTGAACACCGCAGG | 138151 |
| rs746256447 | snp | A/G | 9.29282e-05 | 0.00681582 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011606 | CCCGCCCTGCTCAAA[A/G]GGCTGTGGGGGGCTC | 138151 |
| rs746308207 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136076520 | AGGAAGCAGAACGGA[A/G]GTTTCCAGGGGCTGG | 138151 |
| rs746432687 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136018930 | CCTCGTCTCGAGATG[G/T]TTTTCTAAACAGCAG | 138151 |
| rs746453944 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136093810 | GAAGGGGTGGGTGGC[G/T]GAGAGGTGGCGGGTG | 138151 |
| rs746475671 | snp | A/G | 4.99156e-05 | 0.00499553 | synonymous-codon, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016386 | GCGGCGGATGAGGAC[A/G]CAGGAGCGGCTCTCC | 138151 |
| rs746515923 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136026814 | ATCAGAAAGGAGGGA[C/T]AAGAAAGGAGAAGCA | 138151 |
| rs746526186 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136059972 | GGCGCACGGGGAGCC[A/G]CCTCGGGGGACCTGC | 138151 |
| rs746565582 | in-del | -/TG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136060453 | TGGCAACTGTGAAAC[-/TG]TGGCAGCAGGCGCTT | 138151 |
| rs746604875 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007149 | CATAAAAATCACAAT[C/T]GTGTACGATGCTAAC | 138151 |
| rs746624435 | snp | C/T | 1.70866e-05 | 0.00292284 | missense | NACC2 | GRCh38.p7 | 9:136011836 | CGGCAGGCGGGAACT[C/T]GGGGTCGAGGGGCAC | 138151 |
| rs746630514 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136075229 | TGTCACATGGCACCA[C/G]GGAGGTGGCCAGGAC | 138151 |
| rs746690198 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136079992 | ATGGGCTCTGCTGGC[A/C]ATGGGGCTGCCTGGG | 138151 |
| rs746728669 | snp | A/G | 0.00012751 | 0.00798367 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011864 | CACGCTGGCGGCGGC[A/G]GAGCCCATGACCGTG | 138151 |
| rs746773427 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136077712 | CCGGGAAATGCGAGG[A/G]GACCCCAAGGACTCT | 138151 |
| rs746801239 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136032807 | GAGGCTGAGGTGGGT[A/G]GATCACGAGACTAGC | 138151 |
| rs746888983 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136064968 | GGAAAGAACAGTCTT[C/T]TCAAAATGTGGTGCT | 138151 |
| rs746945465 | in-del | -/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136069587 | ACAAAACAAAAAAAA[-/C]ACCTCACTTCAAATA | 138151 |
| rs746983431 | snp | C/T | 1.7067e-05 | 0.00292117 | synonymous-codon, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013890 | GGTGGCCAGGAGCCT[C/T]CGCAGCAAGACCTTA | 138151 |
| rs747023202 | snp | A/G | 0.00095701 | 0.0218538 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011771 | AGCCACGATGGTGGC[A/G]GCGTCGCCCCGCCGC | 138151 |
| rs747042312 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136091596 | ACCAATACTTCCAGA[A/C]AGATGCCTTCACGCC | 138151 |
| rs747084247 | snp | C/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010212 | TCCCTAACCCTCTGT[C/G]CCCTACCAGTGCCCA | 138151 |
| rs747163150 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136028047 | GGTGGATCACTTGAG[G/T]TCAGAAGTTCGAGAC | 138151 |
| rs747214378 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136068063 | ATAGGACACTTATCA[A/T]GAATGGAACTTGCGG | 138151 |
| rs747240805 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136021755 | AACCATCCACATGAC[A/G]TGTTACCGCTTGGCT | 138151 |
| rs747291922 | snp | A/G | 1.74708e-05 | 0.00295552 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013191 | CCGAGAGACCCCCAG[A/G]CTCTTACATTTCACA | 138151 |
| rs747345379 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136033542 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 138151 |
| rs747374884 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136018777 | CACAGCAAAACAACC[C/T]GGGTGGTATTTTAAA | 138151 |
| rs747471609 | in-del | -/GTGA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024077 | GTGTGAGGCCAGAGT[-/GTGA]GTGAGGGCCAGAGTG | 138151 |
| rs747477091 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136083010 | ATAACTTCTGCCCCA[C/T]TAGACATCTACACTC | 138151 |
| rs747508877 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136061941 | CCTGGCCACCATGGC[A/G]AAATCCCATCCCTAC | 138151 |
| rs747512710 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136017846 | TCCTGCACACCCTAC[C/T]GAGCGCAAGGCCTGC | 138151 |
| rs747523822 | snp | A/G | 1.6914e-05 | 0.00290805 | synonymous-codon, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013275 | GCGGATGCCAGTCCC[A/G]CAGCTGTTGGCCAGC | 138151 |
| rs747524588 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136064504 | TAACAAAAGTAGTGT[-/A]AAAACTCATACTTTG | 138151 |
| rs747553428 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136028824 | TTCCAGGACCTGCTC[C/T]GATTTTGGAGCAAAG | 138151 |
| rs747604133 | snp | C/T | 1.93654e-05 | 0.00311164 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011468 | TGTATTAGTAACGCA[C/T]GCAAGCAGCTCTAGT | 138151 |
| rs747616058 | snp | C/T | 1.9488e-05 | 0.00312148 | missense | NACC2 | GRCh38.p7 | 9:136011526 | TCCGCTTACAAGGTC[C/T]CTGCATAGGTGCCCT | 138151 |
| rs747622899 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136079777 | GGAATAGGAAAGTTA[C/T]GAAATCTTGAAGCCT | 138151 |
| rs747668286 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136088391 | AATTTGAGTCCACAC[A/G]GCAATGCTGGATCCA | 138151 |
| rs747674670 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136075043 | GGCCCAGTAGAGGAC[A/G]TGACCTCCTCCAGGC | 138151 |
| rs747724155 | in-del | -/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136059353 | TCCGGAGCAGGGCCC[-/T]TATGACATGCCAGCT | 138151 |
| rs747778508 | snp | C/G | 1.66233e-05 | 0.00288295 | missense, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016316 | CCGAGTAGAGCTTGG[C/G]ATGGCAGCGGTATCC | 138151 |
| rs747829791 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136066731 | AGAAGTGGAAATACA[C/G]AAATGTCTATCACGG | 138151 |
| rs747831572 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136056679 | CTGGGATGACGGGCC[A/C]CCTCGGACTATCACT | 138151 |
| rs747874602 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136088044 | AGGTGACCTGGAAGA[C/T]GGGCACCCCCAGTGG | 138151 |
| rs747874789 | snp | A/G | 3.32563e-05 | 0.00407763 | missense, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016376 | CCACGAGGTCGCGGC[A/G]GATGAGGACGCAGGA | 138151 |
| rs747907398 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136083796 | GTGGTGGCACGTTCC[A/G]GCCGCCCACGACATT | 138151 |
| rs747912467 | in-del | -/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067267 | AGGGAAACTCTGTCT[-/C]AAAAAAAAAAAAAAA | 138151 |
| rs747937655 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136020199 | GAAAGAACAAATGAA[C/T]GAACGTCAGAAGGAG | 138151 |
| rs747965335 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031387 | CCATCACCCAGGCTG[A/G]GGTGCAGTGGCACAA | 138151 |
| rs748003135 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078989 | CCGCCGCCCCTCTCC[A/G]ATTCCCTAACGGTTC | 138151 |
| rs748055458 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136063214 | GGATGAGCAGCTCCC[A/G]GGACCCCTGGGCTGG | 138151 |
| rs748077807 | snp | A/C | | | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015398 | CCCTACCCCTCCTGG[A/C]CAGGGCAGCCCAACA | 138151 |
| rs748102919 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136071335 | AGATCACGAGGTCAG[C/G]AGTTTGAGACCAGCC | 138151 |
| rs748113732 | snp | C/G | 0.00285714 | 0.0376883 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011645 | GGCGGGCAGCGGCTC[C/G]GGGGCGGCCACCTCC | 138151 |
| rs748164354 | snp | C/G | 2.74789e-05 | 0.00370658 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014007 | GGGCTCGTGGCCTTC[C/G]CGGGCCATAGGGTCC | 138151 |
| rs748165790 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136025336 | ACACGATGTCCGGCC[A/G]TCCATAAGAAAGGGC | 138151 |
| rs748168189 | in-del | -/AAA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031657 | GCCCCATTTTAAGAC[-/AAA]GAAAAAAGAACAAGA | 138151 |
| rs748185485 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136075359 | TCCCCCGAGGCTGGC[G/T]GCTGCGAACTGACTG | 138151 |
| rs748330705 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136020901 | CCATCCGCACCCACA[C/T]GTGGCACCAAAACCA | 138151 |
| rs748437334 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024986 | CTGCTGACTACTAAG[C/T]AGCCATGCATGCAGG | 138151 |
| rs748446765 | in-del | -/AC | | | intron-variant | NACC2 | GRCh38.p7 | 9:136021902 | AACTAAACTTGGGGG[-/AC]AGAGAATCATTTCCA | 138151 |
| rs748465703 | snp | C/T | 4.9884e-05 | 0.00499395 | missense, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016372 | AGGGCCACGAGGTCG[C/T]GGCGGATGAGGACGC | 138151 |
| rs748479729 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136081485 | CAGGAAGGCGGTGCC[A/G]GGCGTCCGCTTCCAC | 138151 |
| rs748490409 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136073988 | GCACAGACTCCGTCA[C/T]GTCCTTGACTATTTT | 138151 |
| rs748509864 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136028777 | GCACAGGCTCAGAAG[C/T]GCCTGCTCCTGCTGC | 138151 |
| rs748580287 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136081247 | AGTCCCGACGGGCAC[C/T]GGGGGCTCCGCAGGA | 138151 |
| rs748585142 | in-del | -/G | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013118 | GCCGGGAGCACCCCC[-/G]GCGGCCCACCCAGTC | 138151 |
| rs748620304 | snp | A/C | 0.000167865 | 0.00915993 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012055 | GGCGTGAGCTCAGCC[A/C]CCTGCCTGCCGGGAG | 138151 |
| rs748638881 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136068668 | CTAAAAACCACTAAA[A/T]TATACAGTGTATGAG | 138151 |
| rs748670981 | snp | A/G | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136095988 | GTTGACAGTCATTCC[A/G]GCACCGGCCACGCAG | 138151 |
| rs748708037 | snp | C/T | 0.000845985 | 0.0205494 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013177 | CCGGCCCCACCCACC[C/T]GAGAGACCCCCAGGC | 138151 |
| rs748736914 | snp | C/G/T | 9.44967e-05 | 0.00687322 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012053 | GCGGCGTGAGCTCAG[C/G/T]CACCTGCCTGCCGGG | 138151 |
| rs748759904 | snp | G/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008802 | ACAGACACTCCCGAC[G/T]CACGCCCACCGTGGG | 138151 |
| rs748843063 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136086737 | CCGTTTCCCTCCCAC[A/G]ACCCCCGCTCAGCTT | 138151 |
| rs748911275 | in-del | -/CA | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010941 | CCCTGCACACACACG[-/CA]CACACACACACTCGT | 138151 |
| rs748939471 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136019670 | CAGCAGCCTCCCGGG[C/T]AGCAGGGCCCAGCTA | 138151 |
| rs748993740 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136065086 | ACCTAAATGTAAGAG[C/T]TAAAACTATAAAACT | 138151 |
| rs749012971 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136071271 | TTAAAAAGGCTGGGC[A/G]CGGTGGCTCACGCCT | 138151 |
| rs749018104 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136017644 | GGTGCTCACATGCCA[C/T]GGTGGACACCAGTCC | 138151 |
| rs749063168 | snp | A/G | 1.66266e-05 | 0.00288323 | synonymous-codon, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016305 | GGGGTCCCCTTCCGA[A/G]TAGAGCTTGGGATGG | 138151 |
| rs749070989 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136062594 | ACCTGTTCTCTGTAC[A/G]TTCACACCAGCCTCA | 138151 |
| rs749103915 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136079702 | GGGTCACCAGAGCCC[C/T]GGAGCGTGGCTGCAG | 138151 |
| rs749105945 | in-del | -/TGT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024526 | GTGTGTGTGTGTGTG[-/TGT]GTGTGGACAGTGTGT | 138151 |
| rs749147235 | snp | A/G | 1.66263e-05 | 0.00288321 | synonymous-codon, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016371 | TAGGGCCACGAGGTC[A/G]CGGCGGATGAGGACG | 138151 |
| rs749172185 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136070278 | TTTGGGAGGCCGAGG[C/T]GGGCGGATGATGAGG | 138151 |
| rs749227087 | snp | G/T | 5.35518e-05 | 0.00517427 | missense | NACC2 | GRCh38.p7 | 9:136011775 | ACGATGGTGGCGGCG[G/T]CGCCCCGCCGCTCGG | 138151 |
| rs749243326 | snp | G/T | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136095705 | CCCGGGAGAGCCCCC[G/T]GGCCCCCCTACCCCG | 138151 |
| rs749254418 | in-del | -/GGCT | 1.6643e-05 | 0.00288465 | frameshift-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016393 | TGAGGACGCAGGAGC[-/GGCT]GGCTCTCCAGCGGCA | 138151 |
| rs749261928 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136079138 | ATGTCTGTGCGTCCC[A/G]TCCTTAACAAGAGAA | 138151 |
| rs749284408 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009939 | CAACAGACATTTCAA[A/G]TCTTGGGATGGGGGG | 138151 |
| rs749290498 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136057218 | TGACCCAAGCAGCCA[C/T]GGCTCACCTGAGGCA | 138151 |
| rs749334664 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136076577 | AATGGGTGCAGTTTC[A/G]GTCAGGGATGATGAA | 138151 |
| rs749383559 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136019920 | AGAAGGACACATCCC[A/G]GGGCTCCACTCGCAG | 138151 |
| rs749460898 | snp | G/T | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013799 | CGATCAGACAGCTCA[G/T]AGCTAAAGGAGCCAG | 138151 |
| rs749479698 | in-del | -/TGT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024528 | GTGTGTGTGTGTGTG[-/TGT]GTGGACAGTGTGTGT | 138151 |
| rs749493803 | snp | A/G | 1.71082e-05 | 0.00292469 | synonymous-codon, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013883 | CAAAGAAGGTGGCCA[A/G]GAGCCTCCGCAGCAA | 138151 |
| rs749580981 | in-del | -/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136066945 | GATCATTTAAAAAGA[-/T]TTAAAAAAAAAAAAA | 138151 |
| rs749582911 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136081415 | TTCCCATCCTCCACG[C/T]GTCCTCCCAGCTGGG | 138151 |
| rs749591024 | snp | A/G | 5.34645e-05 | 0.00517005 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011630 | GGGGCTCTGGCCATC[A/G]GCGGGCAGCGGCTCG | 138151 |
| rs749730449 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067942 | GAGCATGTTACTGTA[C/T]TGAATAGCATAGGCA | 138151 |
| rs749809138 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136020750 | TCAGGGAAGTGGACA[A/G]ACAGGTCAATGGCAC | 138151 |
| rs749850290 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136033028 | ATCTCAAAAAAAAAT[A/G]AGTTGGGCATGGTGG | 138151 |
| rs749858062 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009688 | AAGGAGCCGCCCAGT[A/G]GGAATGCGTCTAACC | 138151 |
| rs749858972 | snp | A/G | 5.02437e-05 | 0.00501192 | synonymous-codon, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136011972 | GCACATGTCCGCGGC[A/G]ATCACGTTCATCTCG | 138151 |
| rs749931223 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136082856 | GGAAAGACAGACACC[A/G]TCTTCCATAAGCAGC | 138151 |
| rs749941648 | snp | A/G | 0.000853323 | 0.0206382 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011741 | CAGGTCAACATTCAC[A/G]GCGTCAGTTCTCAGA | 138151 |
| rs749956560 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136029295 | CTGTGGGTCTCCTCT[C/T]AGCTGAGAGCTGAGC | 138151 |
| rs750042760 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136092261 | CCCAGGACCCAGGGA[C/G]CTGGGTCTGCAGACA | 138151 |
| rs750108386 | snp | C/G | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012752 | TTGGCCACCTGGTGC[C/G]AGCCGGCAGCAGTCA | 138151 |
| rs750112846 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136069871 | CAATTCTAGTAGAGA[A/C]TTCAACAGCCTTCTC | 138151 |
| rs750119761 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010734 | ACATCAGCTGTGCAC[A/G]TCCCACAGTGGGCCC | 138151 |
| rs750179756 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136029841 | GCTCACACACCCCTT[A/G]CTGCTCTGTGCCTGG | 138151 |
| rs750232117 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067128 | GCGTGGTGGTTCATG[C/G]CTGTAATCCCGGCTA | 138151 |
| rs750271882 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136066405 | CACACGCAAAAATAC[G/T]CAGCATCATTAGCCG | 138151 |
| rs750296103 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136019305 | TCAGAGGCCCCGTGA[A/G]TCGGGGCCAGAGCTG | 138151 |
| rs750342472 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136083318 | GTCATCTCCTTGCTC[A/G]GGGAGGCAGCACCGC | 138151 |
| rs750357641 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136075551 | CCAAGCCCAGGCTGT[C/T]GTGCCTGAGGACGCA | 138151 |
| rs750426295 | snp | A/G | 1.94094e-05 | 0.00311517 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011498 | TACTCGGTCCCTCGC[A/G]CAGCCACCCAGCTCC | 138151 |
| rs750449108 | snp | C/G | 6.43687e-05 | 0.00567276 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011855 | GTCGAGGGGCACGCT[C/G]GCGGCGGCGGAGCCC | 138151 |
| rs750452032 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136056338 | CGGCGGCCAGGAACT[A/C]CCCCCAACCCCGAGG | 138151 |
| rs750489805 | snp | G/T | 4.57467e-05 | 0.00478239 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011909 | GCCCTCCGGCAGCAT[G/T]GACTTGATCTTGGGC | 138151 |
| rs750496294 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136058868 | AGCTCAAGCCATGGA[A/G]GGGACGCAGGGGCCG | 138151 |
| rs750516040 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136072130 | ATAATCCCAGCCACT[A/C]GGGAGGCTGAGGCAG | 138151 |
| rs750543283 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136080367 | GGTTCTAGGAAAATC[C/T]GCCCAGCAGCCCACT | 138151 |
| rs750604904 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136025219 | TGGAGAATGTGGGCA[C/T]GGGCGCTGCTGGATG | 138151 |
| rs750685956 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136057032 | GCCCCCACCCCCAGG[C/G]TGGGCCTCCAGCAGC | 138151 |
| rs750762560 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136032378 | ACAATGCAACACTTA[C/G]GAGGAAAAAAAAAAC | 138151 |
| rs750846436 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136065180 | ACACCAAAGAGCAAA[A/G]CAACAAAAGGAAAGA | 138151 |
| rs750864160 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136084356 | AAAGGCGGGTTGCTG[C/G]AGGGCTGCTTCCGAG | 138151 |
| rs750895009 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031876 | CCTGGCTCTGCATTC[C/T]CACCTCCTCTAACTG | 138151 |
| rs750951779 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136083656 | CAGGGCACCACAGGC[A/G]GCTGGCACCACGCTG | 138151 |
| rs750973982 | snp | C/G | 3.35385e-05 | 0.00409489 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011588 | GGGCCTGCTGGGGCC[C/G]CCCCCGCCCTGCTCA | 138151 |
| rs751005537 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136021494 | GGCAGCTGGGACGTC[C/T]TGACCTCACTGGGGA | 138151 |
| rs751006959 | snp | C/T | | | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015958 | GCAACTGGACCCTCG[C/T]GGGGCGGGGGGACTG | 138151 |
| rs751009609 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136063807 | AGAATCACTTGAACC[C/T]GAGAGGTGGAGGTTG | 138151 |
| rs751015206 | snp | A/G | 3.76442e-05 | 0.00433828 | synonymous-codon, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136013965 | TGTGATGTAGACCCC[A/G]GAGCCTGCAGCCACC | 138151 |
| rs751016791 | in-del | -/AA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136026344 | GCAAAACTCCATCTC[-/AA]AAAAAAAAAAAAAAA | 138151 |
| rs751080085 | in-del | -/CA | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007350 | GTGCACGCGCGTGCA[-/CA]CACACAGACACACGC | 138151 |
| rs751093179 | snp | A/G | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012533 | GGTCCCAGGGGCCAC[A/G]TCCACCTCGGTCCCT | 138151 |
| rs751110342 | snp | G/T | 0.000493462 | 0.0156999 | missense | NACC2 | GRCh38.p7 | 9:136011682 | ACCGAGCCAGCCCCG[G/T]CCACCTCCTCGCCGG | 138151 |
| rs751116780 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136059665 | TTCCAGCCGGCCACG[A/G]GGACACCCTGCATAC | 138151 |
| rs751154205 | in-del | -/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136093090 | CAGACCTCAGAGGAA[-/G]GGGCACAAGGTGGAA | 138151 |
| rs751155641 | snp | C/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136006822 | CCTCCTTAAAAAAAA[C/G]ACAAAAAAAAAAAGC | 138151 |
| rs751167313 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136068351 | AAAAAATACAAAAAT[G/T]AGTTGGGCATAGTGG | 138151 |
| rs751229260 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136021376 | CGACGCCAAGTGCCG[G/T]CGAGGATGCGGGGCA | 138151 |
| rs751257183 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136083742 | TGTGCAAGAAGAAAT[-/A]TCCTGCTGTTTCAGG | 138151 |
| rs751273308 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010255 | CCCCAGCCCAGGCCT[A/G]TCCCGGTCATCCCCT | 138151 |
| rs751285949 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136090652 | TCCAACATCAGCTCC[C/T]GAAATGTCCTCAAGC | 138151 |
| rs751344427 | snp | A/G/T | 0.000315329 | 0.0125531 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011942 | CCAGCGCTTGCGAAC[A/G/T]CGGCGGGCGTTGGTG | 138151 |
| rs751350803 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136065533 | GTTGAGGCAGGATAA[C/T]TGCTTGAACCTGAGA | 138151 |
| rs751355540 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136075503 | GTCTCCTACATCGCG[C/G]TACAGTTTCTCAAAC | 138151 |
| rs751434243 | snp | A/G | 7.19373e-05 | 0.00599695 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012040 | CTGTGAGGACGGGGC[A/G]GCGTGAGCTCAGCCA | 138151 |
| rs751484706 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136081529 | AGAATTCCCTCGTGA[C/T]GTTTCTTGGAAATCA | 138151 |
| rs751503519 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136029168 | CCTTTTCCGGGCCCA[C/T]TCATGGCTGCCCATG | 138151 |
| rs751580569 | snp | C/T | 0.000182862 | 0.00956022 | missense, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016364 | TGGCAGGTAGGGCCA[C/T]GAGGTCGCGGCGGAT | 138151 |
| rs751597757 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136023576 | AGCCTGGTCCTGGAG[A/G]CTCAAGAAGTCCCCA | 138151 |
| rs751600124 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136027674 | ATACCTTTATCTGAA[C/T]GATAATGAAAATCTG | 138151 |
| rs751667210 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136021377 | GACGCCAAGTGCCGG[C/T]GAGGATGCGGGGCAG | 138151 |
| rs751676083 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136079536 | AGGCATGGGCACCCC[A/G]TGGCCTGCTGAGAAT | 138151 |
| rs751779484 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136072260 | AAAAAAAAAAAAACC[C/T]AAAGGCAGGGCATGG | 138151 |
| rs751819701 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136066278 | ACTTATATCTAGAAT[A/G]TATAAATAATTCTGA | 138151 |
| rs751829597 | snp | A/G | 1.7067e-05 | 0.00292117 | missense | NACC2 | GRCh38.p7 | 9:136011848 | ACTCGGGGTCGAGGG[A/G]CACGCTGGCGGCGGC | 138151 |
| rs751851288 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136083541 | GCTTCCCAGATTTAG[C/G]GCAGGTCCAGAGGTG | 138151 |
| rs751874029 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136063598 | TTAGGAAATCTCTTA[A/C]AAAGGCCGAGCACGG | 138151 |
| rs751881554 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008211 | ACAGAATTCAAGTAC[C/T]GAGGCACCCAGCCAG | 138151 |
| rs751883614 | in-del | -/G | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013107 | AAGCTGCAGGTGGCC[-/G]GGAGCACCCCCGCGG | 138151 |
| rs751891781 | in-del | -/A | 3.36922e-05 | 0.00410426 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012035 | TACACTGTGAGGACG[-/A]GGGCGGCGTGAGCTC | 138151 |
| rs751940842 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136019528 | CCAGGACGGTGCCCT[C/T]CAAACCTCTCAGCAT | 138151 |
| rs751987387 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136093331 | GGGAGGATTGAAGAA[G/T]TTTTTAAAAGTCACC | 138151 |
| rs752054450 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136063024 | TGTCTCCCCAAGAGA[A/G]GAAGCCCGACTTTGC | 138151 |
| rs752059608 | in-del | -/GTGT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024502 | GTGTGTGAGGACAGA[-/GTGT]ATGTGTGTGTGTGTG | 138151 |
| rs752063963 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136061840 | ACGAAAAGTTGGTGG[C/T]CGGGCGCGGTGGCTC | 138151 |
| rs752067988 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078211 | CCGGGTGCATACCCA[C/T]CACCTGGCAGGGGTC | 138151 |
| rs752094797 | snp | A/G | 1.70165e-05 | 0.00291684 | missense, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013258 | GGGTCGCTGGTGGAC[A/G]AGCGGATGCCAGTCC | 138151 |
| rs752097153 | snp | C/T | | | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006203 | CAATAAAACCAAGGT[C/T]CCGAAAAGGAGACCC | 138151 |
| rs752120950 | in-del | -/AAAAAAAAAAAAAAAG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136033654 | ACTCTGTCTCAAAAA[-/AAAAAAAAAAAAAAAG]AACTTCTAGGAATAA | 138151 |
| rs752147481 | in-del | -/AAAAT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136033181 | CCCTGTCTCAAAAAT[-/AAAAT]AAAATAAAATAAAAT | 138151 |
| rs752170986 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136025148 | CCAGGCTTTCAGCTG[A/G]GGCCCTGGAAGGGCT | 138151 |
| rs752189354 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136062751 | AAACCCCATCTCTAC[-/A]AAAAAAATACAAAGA | 138151 |
| rs752222509 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010033 | AAGGGAGGGACACCT[A/G]GGTAGGTGGCCACAC | 138151 |
| rs752234543 | snp | C/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136006920 | TATTTTTTAACAGTC[C/G]TGAGTTACAGTACTT | 138151 |
| rs752287451 | snp | C/T | 1.8392e-05 | 0.00303243 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013830 | AACCCTCCGCAGCTC[C/T]ATTGTGCCCTCCAGC | 138151 |
| rs752312569 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136020559 | GGGGTAGGAGGGAGA[C/T]GGGGAGGCCTACTCC | 138151 |
| rs752337612 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067396 | TGTTCTAAAATTCAC[A/G]ATGGTAATGGTTGCA | 138151 |
| rs752348350 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031641 | CTGTGCCCGGCCCAC[A/G]GCCCCATTTTAAGAC | 138151 |
| rs752383989 | snp | C/G | 2.82187e-05 | 0.00375614 | missense | NACC2 | GRCh38.p7 | 9:136011570 | CGCGGCCGCCGGCGT[C/G]TGGGGCCTGCTGGGG | 138151 |
| rs752390138 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136023194 | CCGGATGGAAAGGGG[A/C]TCGCTGGTCTCTCGA | 138151 |
| rs752426411 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136084192 | CGATGAGACCCTCAA[C/T]ACCCACTCACCAACC | 138151 |
| rs752442192 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136081164 | CCAAACGGACCCTCA[A/G]TGGCCACTCGGGGAC | 138151 |
| rs752478360 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136073491 | GCTGCAGTGGACAGG[G/T]GGTGTGAGCGTGGAT | 138151 |
| rs752519453 | snp | A/G | | | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014693 | GAGCCCTCAGGCAAC[A/G]ATGAGGGAGACGGAA | 138151 |
| rs752534164 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136026649 | ACAATGATGTAAAAT[A/G]ACAAAGGCACGTCTA | 138151 |
| rs752649411 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136093916 | AGAATGCTGAGCTGA[A/G]TGTCCCACTGGAGAA | 138151 |
| rs752725060 | snp | A/C | 3.59176e-05 | 0.00423763 | missense | NACC2 | GRCh38.p7 | 9:136011931 | ATCTTGGGCAGCCAG[A/C]GCTTGCGAACGCGGC | 138151 |
| rs752870946 | in-del | -/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136057648 | AGCTCCAGCGCAGGG[-/C]CCCCTCCTCCCCCAG | 138151 |
| rs752889119 | snp | A/G | 1.66466e-05 | 0.00288496 | synonymous-codon, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016290 | CTCCAGCTTCTCCCC[A/G]GGGTCCCCTTCCGAG | 138151 |
| rs752909226 | in-del | -/ATCA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136017810 | TGCCTTCACTAGGGA[-/ATCA]ATCCCACTGCCCTGG | 138151 |
| rs752911225 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136032712 | GACCAGCCCATCCAA[C/T]ATGGTGAAACCCCAT | 138151 |
| rs752924990 | snp | C/G | 0.000657061 | 0.0181135 | missense | NACC2 | GRCh38.p7 | 9:136011762 | AGTTCTCAGAGCCAC[C/G]ATGGTGGCGGCGTCG | 138151 |
| rs752971717 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136092523 | CTTTGCTTCTCCTTC[C/G]AGCCACGCCTGGAAG | 138151 |
| rs752978966 | snp | C/T | 4.99255e-05 | 0.00499603 | synonymous-codon, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016356 | GATGAGGCTGGCAGG[C/T]AGGGCCACGAGGTCG | 138151 |
| rs753025661 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136017247 | TGCAGCGCGACCCCG[A/G]TGGCACCACGCGTCA | 138151 |
| rs753039323 | in-del | -/AGTG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024155 | TGTGTGTGGGGACAG[-/AGTG]TGTGTGTGTGTGTGT | 138151 |
| rs753162522 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136091639 | TCTGCTGAGACCCTA[C/T]ACAAGGGTGTGTGCT | 138151 |
| rs753193316 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136069957 | ATCAGCAGGATCTAA[A/C]TGACATTACAGAACT | 138151 |
| rs753216369 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136090520 | CTAGCATTTTGTGGG[A/G]TGGGGGCTGGGTTGC | 138151 |
| rs753222545 | snp | A/G | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013107 | AAGCTGCAGGTGGCC[A/G]GGAGCACCCCCGCGG | 138151 |
| rs753266857 | in-del | -/CAGACGCACA | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007457 | GCACACACACGCGCA[-/CAGACGCACA]CACAGACGCACACAC | 138151 |
| rs753310693 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136022319 | TGACCACACTCTCCA[C/G]ATGGGGCTGTGTCCC | 138151 |
| rs753375913 | snp | A/C | 0.000111045 | 0.00745052 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013170 | CCCAGCCCCGGCCCC[A/C]CCCACCCGAGAGACC | 138151 |
| rs753401574 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136019456 | TCACCCCAGGACTGG[C/T]CGCTGTAGCAGAACT | 138151 |
| rs753445442 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136030364 | CCTGTAATCCCAGCA[C/T]TTTGCGAGGCCAAGG | 138151 |
| rs753449087 | in-del | -/GGAT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136021380 | GCCAAGTGCCGGCGA[-/GGAT]GCGGGGCAGCTGGGA | 138151 |
| rs753461006 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136083487 | TGACTGTATTTGGAA[C/G]TAGGGTCTTTGCAGA | 138151 |
| rs753477800 | snp | C/T | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013118 | GGCCGGGAGCACCCC[C/T]GCGGCCCACCCAGTC | 138151 |
| rs753535322 | snp | A/G | 1.70638e-05 | 0.00292089 | synonymous-codon, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013251 | CCGGCTGGGGTCGCT[A/G]GTGGACGAGCGGATG | 138151 |
| rs753535381 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136029501 | AGAGATGAAAGAGCT[A/G]TAACACAAACAGGGC | 138151 |
| rs753565129 | snp | A/C | 1.9418e-05 | 0.00311587 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011505 | TCCCTCGCGCAGCCA[A/C]CCAGCTCCGCTTACA | 138151 |
| rs753603600 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136080445 | GGCGTGGTGGCGCAC[A/G]CCTGCAATCCCAGCT | 138151 |
| rs753666364 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136058203 | GTTGGGCAGCAGGGA[A/G]CCCAGGCTATGTCCT | 138151 |
| rs753783294 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136088296 | GATGGAAGGGATGAC[A/G]GGGGCAGGGGACACA | 138151 |
| rs753863355 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067186 | TTGAACCCGGGAGGC[A/G]GACGTTGCGGTGAGC | 138151 |
| rs753878775 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009404 | AGGTCTGGATGCCTC[C/T]GCACCACTGAGCCAC | 138151 |
| rs753978367 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136082564 | TGGCCCTCGGAGCCC[A/G]ACAAACAAAACCAGG | 138151 |
| rs754097854 | snp | A/C | | | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015389 | AAGGTGGGCCCCTAC[A/C]CCTCCTGGCCAGGGC | 138151 |
| rs754162071 | snp | A/T | 1.66696e-05 | 0.00288696 | missense, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016270 | GCAGCCTCACCTGCC[A/T]CCAGCTCCAGCTTCT | 138151 |
| rs754191859 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136068611 | GAGCAACACTGTATA[C/T]GCTGTCCCCTGAACT | 138151 |
| rs754243688 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011058 | CCTGAGCCCTGCCCC[A/G]TCGCCCCAGAGAGGT | 138151 |
| rs754265404 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136022179 | CTTGGTGGCATCAGG[C/T]GCAGAGCAGGTGCAC | 138151 |
| rs754289446 | in-del | -/CTT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136080279 | CATCTCTGTGCTCTC[-/CTT]CTCTGAGCCCAGGCC | 138151 |
| rs754330400 | in-del | -/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136056463 | GCGGGGCCAGGCCCC[-/T]AGCCATCATCCTTCC | 138151 |
| rs754359075 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136021530 | CAAAGTGGCATGGCC[A/C]CTCTGGAAAACTGCT | 138151 |
| rs754363654 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136077599 | CAAGAAAAGGGAAAC[A/G]CACAGAGGAGGGAGG | 138151 |
| rs754398812 | in-del | -/C | | | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006215 | GTCCCGAAAAGGAGA[-/C]CCCCCCGACCCTGGC | 138151 |
| rs754409552 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136057266 | CACGCTCATCTCTAA[C/T]CTTCACTTGCAGAAT | 138151 |
| rs754417153 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136088356 | AGACCCCACTCCCTG[C/T]CTCTCTCCCCTAGGG | 138151 |
| rs754430292 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009405 | GGTCTGGATGCCTCT[A/G]CACCACTGAGCCACC | 138151 |
| rs754432661 | snp | A/G | 7.31823e-05 | 0.00604862 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011795 | CCGCCGCTCGGCGTA[A/G]ATGCGTTGCTCGAAC | 138151 |
| rs754519858 | snp | C/T | 1.82667e-05 | 0.00302209 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013171 | CCAGCCCCGGCCCCA[C/T]CCACCCGAGAGACCC | 138151 |
| rs754574288 | in-del | -/AG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024346 | TGTGTGTGTGAGGAC[-/AG]AGTGTGTGTGTGTGA | 138151 |
| rs754609505 | snp | A/G | 1.70598e-05 | 0.00292055 | missense, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013252 | CGGCTGGGGTCGCTG[A/G]TGGACGAGCGGATGC | 138151 |
| rs754642389 | snp | C/G | 1.94245e-05 | 0.00311638 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011510 | CGCGCAGCCACCCAG[C/G]TCCGCTTACAAGGTC | 138151 |
| rs754648236 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136030369 | AATCCCAGCACTTTG[C/T]GAGGCCAAGGCAGGC | 138151 |
| rs754706322 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136026439 | CTTGGGGAAAGCCTA[A/G]CATACATGTAACTGG | 138151 |
| rs754717945 | in-del | -/CGCCGC | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078968 | GCCGGCATGATGCCG[-/CGCCGC]CGCCGCCGCCGCCCC | 138151 |
| rs754759517 | in-del | -/AA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136066203 | ATCTCAAAAAAAAAA[-/AA]AGAAAGAAAGAAAAA | 138151 |
| rs754840000 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136071272 | TAAAAAGGCTGGGCG[C/T]GGTGGCTCACGCCTA | 138151 |
| rs754866813 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136025324 | TCACCTGTTTTCACA[A/C]GATGTCCGGCCGTCC | 138151 |
| rs754873925 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136092761 | TGGGGTCTGTAGAAG[A/G]CCTTGGTTCTCCGGA | 138151 |
| rs754883808 | snp | C/T | 0.000130141 | 0.00806556 | missense | NACC2 | GRCh38.p7 | 9:136011857 | CGAGGGGCACGCTGG[C/T]GGCGGCGGAGCCCAT | 138151 |
| rs754895578 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136088851 | ACCTACCCCAAGCCC[C/T]GAGGGGAGCCAGCCC | 138151 |
| rs754937337 | snp | A/G | 8.44523e-05 | 0.00649762 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011822 | GAACACCTGTGCCGC[A/G]GCAGGCGGGAACTCG | 138151 |
| rs754938896 | in-del | -/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009948 | TTCAAGTCTTGGGAT[-/G]GGGGGGTTCTTCTGG | 138151 |
| rs754952261 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136086133 | ACCAAGTCACCCCTG[A/G]GGACCCTTGTTGGAC | 138151 |
| rs755026968 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136077616 | ACAGAGGAGGGAGGG[A/G]CAAGAGCCCAGAACA | 138151 |
| rs755055335 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136082590 | CCAGGTAGAGCCGAG[A/G]CGTCTTAGCAGGTGC | 138151 |
| rs755075541 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136032694 | TTGAGATCAGGAGTT[C/T]GAGACCAGCCCATCC | 138151 |
| rs755096254 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136068319 | CCTGGTCAACATGGC[A/G]AAACCCTGTCTCTAC | 138151 |
| rs755116853 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136084454 | GGCGGTATCTCTGAC[A/G]TCCCTGCCCAAGACG | 138151 |
| rs755139596 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136064728 | GCTGATGCTAAAAAT[G/T]CATATGGAAACGCAA | 138151 |
| rs755148968 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136069463 | CTGAGGCAGGAGAAT[C/T]GCTTGAAACCAGAAG | 138151 |
| rs755165066 | snp | C/G | 9.99917e-05 | 0.00707007 | synonymous-codon, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016272 | AGCCTCACCTGCCAC[C/G]AGCTCCAGCTTCTCC | 138151 |
| rs755168408 | snp | C/G | | | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015396 | GCCCCTACCCCTCCT[C/G]GCCAGGGCAGCCCAA | 138151 |
| rs755221201 | snp | A/G | 2.61414e-05 | 0.00361525 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014000 | AGAAAAAGGGCTCGT[A/G]GCCTTCCCGGGCCAT | 138151 |
| rs755223596 | snp | A/G | | | synonymous-codon, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016293 | CAGCTTCTCCCCGGG[A/G]TCCCCTTCCGAGTAG | 138151 |
| rs755235737 | snp | C/T | 0.000130796 | 0.00808584 | missense | NACC2 | GRCh38.p7 | 9:136011698 | CCACCTCCTCGCCGG[C/T]GTCGAAGGCGGGGTT | 138151 |
| rs755265435 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136049318 | TCCCGTACACCGCGT[A/G]GCGCCAGGCCCTTCA | 138151 |
| rs755276369 | in-del | -/TT | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136097209 | GCTCTGTTTATTCCT[-/TT]TTTTTTTTTTTTTTT | 138151 |
| rs755299048 | snp | C/G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136091635 | GCGCTCTGCTGAGAC[C/G/T]CTATACAAGGGTGTG | 138151 |
| rs755311226 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136057579 | AATTTAAATAACGTA[A/G]GCTTGAAGAGCGTCT | 138151 |
| rs755338366 | in-del | -/AC | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007433 | CGCGTGCACACATAC[-/AC]ACAGACGCGCACACA | 138151 |
| rs755473827 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067988 | GAAGCATTTGTGTAT[C/T]GAAACATAGTAAAGG | 138151 |
| rs755476015 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136022180 | TTGGTGGCATCAGGC[A/G]CAGAGCAGGTGCACA | 138151 |
| rs755534705 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136088873 | AGCCAGCCCAGCCCC[C/T]GGCATCCTGGGGGAA | 138151 |
| rs755558133 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136018436 | GAATCCACAGCGGGC[A/G]CCCCACTGAAGGCAG | 138151 |
| rs755654172 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008694 | AGGCACTCTGGAAGG[C/T]CCCTCTGAGCCCGGG | 138151 |
| rs755716518 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136017439 | GCATGCACCAGGTGC[A/G]CGGGGCCAAGGAAAC | 138151 |
| rs755718730 | snp | C/T | 4.26867e-05 | 0.00461969 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012048 | ACGGGGCGGCGTGAG[C/T]TCAGCCACCTGCCTG | 138151 |
| rs755721510 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136082875 | TCCATAAGCAGCTGA[A/G]TGTATTTCTGCTCAT | 138151 |
| rs755729839 | in-del | -/C | 1.86485e-05 | 0.00305351 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013817 | CTAAAGGAGCCAGAA[-/C]CCTCCGCAGCTCCAT | 138151 |
| rs755804128 | snp | A/C | 5.57927e-05 | 0.0052814 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013162 | GATCTGAACCCAGCC[A/C]CGGCCCCACCCACCC | 138151 |
| rs755813704 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136081747 | GGGCACCATCCCCAC[C/T]AAGTGGCGGCAGCAG | 138151 |
| rs755837397 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136057932 | CCAGCCCATTAGAGA[C/T]GGCGACTTCGCGGCA | 138151 |
| rs755859241 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136091101 | GGTCCCTGCAAACAA[A/C]CTCTGGAGAAAAGCC | 138151 |
| rs755989525 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136027556 | ATTCAGAATTCATAA[C/T]AAAAAAGATGACCAG | 138151 |
| rs756007174 | in-del | -/TT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136028376 | TTTGCCTTTGCTTCC[-/TT]TTTTTTTTTTTTTTT | 138151 |
| rs756078697 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136094142 | CCCCGCCACACACAG[G/T]AAGGAACGCGCAGCA | 138151 |
| rs756107345 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136070781 | GGAGGAAAAAAATCA[A/G]TGAAACAGCTGGGTT | 138151 |
| rs756119205 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136058873 | AAGCCATGGAGGGGA[C/T]GCAGGGGCCGGGGCA | 138151 |
| rs756175440 | snp | C/G | 1.65701e-05 | 0.00287833 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011921 | CATGGACTTGATCTT[C/G]GGCAGCCAGCGCTTG | 138151 |
| rs756265081 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136072131 | TAATCCCAGCCACTC[G/T]GGAGGCTGAGGCAGG | 138151 |
| rs756333106 | in-del | A/CAGGACAGGACAGGAC | | | intron-variant | NACC2 | GRCh38.p7 | 9:136062157 | CAGGACAGGACAGGA[A/CAGGACAGGACAGGAC]AGGAAAGGAAAGAGA | 138151 |
| rs756426218 | snp | A/C | 1.75019e-05 | 0.00295815 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013859 | GCACTCCTGCCCCGA[A/C]CTACCTGTCAAAGAA | 138151 |
| rs756450258 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010293 | GCCTCAGGCACCCTC[C/T]ATCCATGCACACCCC | 138151 |
| rs756506730 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136020597 | TGTATACCATTTGTT[A/G]AAATGCACCACAAGA | 138151 |
| rs756585405 | snp | G/T | 2.28621e-05 | 0.00338091 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136013994 | CCAAACAGAAAAAGG[G/T]CTCGTGGCCTTCCCG | 138151 |
| rs756595930 | snp | A/G | 1.95502e-05 | 0.00312645 | missense | NACC2 | GRCh38.p7 | 9:136011616 | TCAAAGGGCTGTGGG[A/G]GGCTCTGGCCATCGG | 138151 |
| rs756602931 | in-del | -/AA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136028212 | AGAAACTCCATCTCC[-/AA]AAAAAAAAAAAAAAA | 138151 |
| rs756667826 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136077395 | AACAAACAAACAAAC[-/A]AACAAAAACCCTAAC | 138151 |
| rs756668265 | in-del | -/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136089500 | ACAACCCCACCTGGT[-/G]GGGGGGCTCCTGTTA | 138151 |
| rs756672168 | snp | C/T | 1.77704e-05 | 0.00298075 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011684 | CGAGCCAGCCCCGTC[C/T]ACCTCCTCGCCGGCG | 138151 |
| rs756673993 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136073822 | AGTACTGCATTTGCG[C/T]CCAAGCAGGATTTGG | 138151 |
| rs756685962 | snp | A/G | 0.000637823 | 0.0178467 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011693 | CCCGTCCACCTCCTC[A/G]CCGGCGTCGAAGGCG | 138151 |
| rs756744495 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136081549 | CTTGGAAATCAGTGG[C/T]TGTAATCACAGCTGC | 138151 |
| rs756757910 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136081112 | TTCCCATATTTCTCG[A/T]AACACAGGAAACCAT | 138151 |
| rs756856733 | snp | G/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136006966 | CTCTTTAAAACAACC[G/T]TCTCCTTTTTAAAAG | 138151 |
| rs756872149 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008236 | AGCCAGGCGCGGCCC[A/G]CCGGGCTCACAGTAT | 138151 |
| rs756880419 | in-del | -/CAGC | 0.00021347 | 0.0103291 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012050 | GGGGCGGCGTGAGCT[-/CAGC]CACCTGCCTGCCGGG | 138151 |
| rs756881037 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008468 | CTATATAGGATATGC[A/G]TATTGCTAATAGTCA | 138151 |
| rs756888238 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136026865 | AGCAGAGACCAATGG[A/G]CAAGACGGTAGATTA | 138151 |
| rs756940764 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136059803 | ATGAGCATGTCACCC[A/G]GCTTCCCCAGCCCTC | 138151 |
| rs756963940 | in-del | -/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136094289 | GGGAGGCCAACTCCA[-/G]GGACCCGGCCTCGCG | 138151 |
| rs756967298 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011041 | GGAGTTAGGCCCTGG[A/G]GCCTGAGCCCTGCCC | 138151 |
| rs757007781 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136056355 | CCCCAACCCCGAGGC[C/T]CCCACAAAAGCCAGG | 138151 |
| rs757098766 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136027206 | CTCCAGCCTGGACGA[C/T]GGAGCAAGACTCTGT | 138151 |
| rs757101639 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136065545 | TAATTGCTTGAACCT[C/G]AGAGGCAGAGGTTGT | 138151 |
| rs757115494 | in-del | -/AA/ACAG | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007542 | CAGACGTGCACACAC[-/AA/ACAG]AGACACGCACACACA | 138151 |
| rs757243019 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136043477 | CGGCTGCCGTAAGGC[C/T]GTGGGGCGCCTGCTG | 138151 |
| rs757245991 | in-del | -/AC | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007359 | CGTGCACACACACAG[-/AC]ACACGCGTGCACACA | 138151 |
| rs757261180 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136092674 | GTGCTACCAAGGTGA[A/G]GGTGGACTGGGCCGG | 138151 |
| rs757286030 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136017355 | GTCAGGGTCACAGAG[C/T]CCCTCTAGAGCGTTC | 138151 |
| rs757307448 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136056717 | CAGCCTGGGAGGTGG[A/G]GGAGAGCCATGCAGG | 138151 |
| rs757368830 | snp | C/T | 4.26267e-05 | 0.00461644 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011819 | CTCGAACACCTGTGC[C/T]GCGGCAGGCGGGAAC | 138151 |
| rs757373414 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136071092 | TTAAAAATTCGCCAG[A/G]CATGGTGGCTCATGC | 138151 |
| rs757437292 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136022661 | TGGTCAGTGTCCCCA[A/G]GGCCTGGCACACAGC | 138151 |
| rs757456963 | snp | C/T | 6.19138e-05 | 0.00556355 | missense | NACC2 | GRCh38.p7 | 9:136011851 | CGGGGTCGAGGGGCA[C/T]GCTGGCGGCGGCGGA | 138151 |
| rs757463479 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136079560 | TGAGAATGACACGAA[C/G]GAACAGGCTGACTCA | 138151 |
| rs757549701 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078979 | TGCCGCGCCGCCGCC[A/G]CCCCTCTCCGATTCC | 138151 |
| rs757613602 | snp | A/G | 1.68826e-05 | 0.00290534 | synonymous-codon, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013289 | CGCAGCTGTTGGCCA[A/G]CGTGTTCCTGGTGGA | 138151 |
| rs757659835 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136085709 | TACCTCAAATCGTTC[A/G]GGAAAATGTTCTTTG | 138151 |
| rs757749581 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136093345 | ATTTTTTAAAAGTCA[A/C]CACTAGCCCCCTGCC | 138151 |
| rs757785927 | snp | C/T | 3.4219e-05 | 0.00413622 | missense | NACC2 | GRCh38.p7 | 9:136011589 | GGCCTGCTGGGGCCG[C/T]CCCCGCCCTGCTCAA | 138151 |
| rs757791112 | in-del | -/GACAG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136062120 | AACAGAGCGAGACAG[-/GACAG]GACAGGACAGGACAG | 138151 |
| rs757791455 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136080517 | GCAGAGGTTGTGTGC[C/T]GAGATCGTGCCACTG | 138151 |
| rs757836239 | snp | A/C | 5.43739e-05 | 0.00521383 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013842 | CTCCATTGTGCCCTC[A/C]AGCACTCCTGCCCCG | 138151 |
| rs757946382 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136025348 | GCCGTCCATAAGAAA[A/G]GGCCAGGAATCCCAG | 138151 |
| rs757949755 | snp | C/T | 1.94448e-05 | 0.00311802 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011519 | ACCCAGCTCCGCTTA[C/T]AAGGTCCCTGCATAG | 138151 |
| rs758027527 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136023229 | CCATGCCCACACTCA[C/T]GGGTGCAGCTGCGGG | 138151 |
| rs758074494 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009496 | GGGGCCGAGGTTAGC[A/G]TCCACAGTGCCTGCC | 138151 |
| rs758146244 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136064800 | AAGTTAGAGCAGTCA[G/T]ACTTCCCAATTTCTG | 138151 |
| rs758154109 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136081229 | AAGGAACCAGGTGGA[C/T]TCAGTCCCGACGGGC | 138151 |
| rs758224137 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067753 | GGCAGGAGAATCACT[C/T]GAACCCGGGAGGCGG | 138151 |
| rs758240411 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136073504 | GGGGGTGTGAGCGTG[A/G]ATCCAGCTGTATCAG | 138151 |
| rs758410673 | snp | G/T | 1.65573e-05 | 0.00287721 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011936 | GGGCAGCCAGCGCTT[G/T]CGAACGCGGCGGGCG | 138151 |
| rs758429315 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136026703 | ATTAACACACAGAAC[A/G]TTCTAACTCAGGATG | 138151 |
| rs758440247 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136072187 | AGGTTGCAGTTAGCC[A/G]AGATCGTGCCATTGC | 138151 |
| rs758450895 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136068676 | CACTAAATTATACAG[C/T]GTATGAGTGAATTGT | 138151 |
| rs758505184 | snp | C/G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078961 | GCACCGTCGCCGGCA[C/G/T]GATGCCGCGCCGCCG | 138151 |
| rs758524818 | snp | C/T | 3.32718e-05 | 0.00407858 | missense, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016295 | GCTTCTCCCCGGGGT[C/T]CCCTTCCGAGTAGAG | 138151 |
| rs758548971 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078167 | GAGTGGGATGGACCA[A/G]GCACCCACTCAAACC | 138151 |
| rs758561239 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136072266 | AAAAAACCCAAAGGC[-/A]AGGGCATGGTGGCTC | 138151 |
| rs758564791 | snp | A/G | 7.3373e-05 | 0.00605649 | missense | NACC2 | GRCh38.p7 | 9:136011800 | GCTCGGCGTAGATGC[A/G]TTGCTCGAACACCTG | 138151 |
| rs758618102 | snp | C/G | 1.66225e-05 | 0.00288287 | missense, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016358 | TGAGGCTGGCAGGTA[C/G]GGCCACGAGGTCGCG | 138151 |
| rs758627605 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136061206 | CGGCTACCGGGGTCT[C/T]CCACTGCCTGGTCGG | 138151 |
| rs758632051 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136065492 | AGATGTGGTGGCGCA[C/T]GCCAGTAGTCCCAGC | 138151 |
| rs758699733 | in-del | -/AAA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067268 | GGGAAACTCTGTCTC[-/AAA]AAAAAAAAAAAAAAA | 138151 |
| rs758712563 | in-del | -/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136032536 | GATATGTAAGAAGTT[-/C]TGGCCAGTTCAATGA | 138151 |
| rs758715347 | in-del | -/TCAA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136017811 | GCCTTCACTAGGGAA[-/TCAA]TCCCACTGCCCTGGG | 138151 |
| rs758728161 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136029586 | GCCCTTCGGGGATCC[A/C]AGACCCAGGAGGTCC | 138151 |
| rs758755804 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136062872 | CAGTGTGCCGTGATC[A/G]TGCCACTGTACTCCA | 138151 |
| rs758782409 | in-del | -/GT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024161 | GGGGACAGAGTGTGT[-/GT]GTGTGTGTGTGTGTG | 138151 |
| rs758821182 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136092644 | GGTCAGCCTGGGCCA[C/T]TGAGGCAGGGACATG | 138151 |
| rs758823741 | snp | A/G | 3.58584e-05 | 0.00423413 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013178 | CGGCCCCACCCACCC[A/G]AGAGACCCCCAGGCT | 138151 |
| rs758836259 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136069968 | CTAACTGACATTACA[A/G]AACTCTCCACTCAAC | 138151 |
| rs758913203 | snp | C/T | | | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014280 | CCATGCTGCGGTCCC[C/T]GGCCTCAGCTCCCTC | 138151 |
| rs758939313 | in-del | -/G | 5.86826e-05 | 0.00541644 | frameshift-variant | NACC2 | GRCh38.p7 | 9:136011612 | TGCTCAAAGGGCTGT[-/G]GGGGGGCTCTGGCCA | 138151 |
| rs758971834 | snp | A/G | 1.70003e-05 | 0.00291545 | synonymous-codon, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013260 | GTCGCTGGTGGACGA[A/G]CGGATGCCAGTCCCG | 138151 |
| rs759025778 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136070213 | AGAAGAAGTCTCAAG[-/A]AAATCAAATACGGGC | 138151 |
| rs759028905 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136020536 | TGGAGCCCAGCAGAG[C/T]CTCGGCGGGGGTAGG | 138151 |
| rs759109375 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136083492 | GTATTTGGAACTAGG[A/G]TCTTTGCAGATGTAA | 138151 |
| rs759120815 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031606 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGTGTGA | 138151 |
| rs759184252 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136093923 | TGAGCTGAGTGTCCC[A/C]CTGGAGAACAGGAGG | 138151 |
| rs759190087 | snp | C/T | 3.7246e-05 | 0.00431528 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013822 | GGAGCCAGAACCCTC[C/T]GCAGCTCCATTGTGC | 138151 |
| rs759192166 | in-del | -/AAAA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136071544 | TGAGACTCCATCTCA[-/AAAA]AAAAAAAAAAAAAAA | 138151 |
| rs759195071 | in-del | -/CA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067267 | AGGGAAACTCTGTCT[-/CA]AAAAAAAAAAAAAAA | 138151 |
| rs759225614 | snp | C/T | | | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014516 | CTGGTCTTGAACACC[C/T]GGCCTCAAGCAATCT | 138151 |
| rs759280151 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136091062 | TCCTTTAGAGAGACC[C/T]GGAGCCAGCCTCTCC | 138151 |
| rs759289836 | snp | A/G | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096859 | AGAGACAGATGCCTG[A/G]AGCTGCTTCCAGCCC | 138151 |
| rs759290503 | snp | A/G | 2.41987e-05 | 0.00347833 | missense | NACC2 | GRCh38.p7 | 9:136011565 | CGGGCCGCGGCCGCC[A/G]GCGTCTGGGGCCTGC | 138151 |
| rs759290558 | snp | A/C | 1.6507e-05 | 0.00287284 | missense, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013941 | GTGGCAGTTCATCAG[A/C]TGGCCGCGTGTGATG | 138151 |
| rs759312287 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136059432 | GAGCCCAGACCTGGC[A/G]CTCCTGAGAAAGTGG | 138151 |
| rs759338805 | snp | A/C | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010878 | GTAAAGTACCCTTTT[A/C]TCCACCCCGAGGGGT | 138151 |
| rs759364169 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136089581 | CGGGGTGCCCTCCCT[C/T]CTCTGAGGCTCCCCC | 138151 |
| rs759382659 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136060342 | GGAGGCCCTGGAGCC[A/G]GCTGGGCTGCCTTTA | 138151 |
| rs759406380 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136077879 | TACGCAAAGGTGTGC[C/T]TTTGGGAGTGAAAAC | 138151 |
| rs759435250 | snp | C/T | 4.25188e-05 | 0.0046106 | missense | NACC2 | GRCh38.p7 | 9:136011659 | CGGGGGCGGCCACCT[C/T]CTGGATGACCGAGCC | 138151 |
| rs759466935 | in-del | -/GCCG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136029736 | GCAGCCCTGCAGGGA[-/GCCG]GCCGGCGCCTGTGCC | 138151 |
| rs759468793 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136068140 | ACTGGGATATTACTA[C/T]ATGCTACTAAAGACT | 138151 |
| rs759500139 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136065449 | ACATGGTAAGATCCC[A/G]TCTCTACTAAAAATA | 138151 |
| rs759670775 | in-del | -/GACG | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007462 | ACACACGCGCACACA[-/GACG]CACACACACAGACGC | 138151 |
| rs759718194 | snp | A/C | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096965 | TATTTTCTAAATATT[A/C]AAGACATTCTTCCTT | 138151 |
| rs759830776 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136027424 | CTTCCTTATCAGCAC[C/T]GTTTATGCTATTTCT | 138151 |
| rs759868500 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136087861 | TCTGAGCTGCTCGAG[A/G]GAGGGCAAGCCCTCC | 138151 |
| rs759991882 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078864 | CTCTCGCCCCTTGTC[C/T]AGGCGACCTTGTGGG | 138151 |
| rs760049815 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136056723 | GGGAGGTGGAGGAGA[A/G]CCATGCAGGGCTGGG | 138151 |
| rs760081992 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136086925 | ACCACACCGGGGGTT[C/T]GCATCTACCTGACCC | 138151 |
| rs760227949 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136092299 | CCGGGGAGCCTGACC[A/G]GAGATGGGGTGAGAG | 138151 |
| rs760269236 | in-del | -/GT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024094 | AGTGAGGGCCAGAGT[-/GT]GTGTGTGTGTGTGGG | 138151 |
| rs760271960 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136093209 | GGAAAGCAGGACTCC[A/G]GAGGCAGAGGCCAAG | 138151 |
| rs760323209 | snp | C/T | | | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014758 | GGGCCCAGTGCTGAC[C/T]TCCTCTGGGTATGTG | 138151 |
| rs760344701 | snp | C/T | 3.4191e-05 | 0.00413453 | missense, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013247 | GCTTCCGGCTGGGGT[C/T]GCTGGTGGACGAGCG | 138151 |
| rs760440213 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024725 | CAGAGATTCCCACTG[C/T]GGATATGAGGGAGCA | 138151 |
| rs760448840 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067146 | GTAATCCCGGCTACT[C/T]GGGAGGCTGAGGCAG | 138151 |
| rs760471291 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136020204 | AACAAATGAACGAAC[A/G]TCAGAAGGAGGGGGC | 138151 |
| rs760500139 | snp | C/G | 1.94082e-05 | 0.00311508 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011501 | TCGGTCCCTCGCGCA[C/G]CCACCCAGCTCCGCT | 138151 |
| rs760566961 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136073623 | GACAAAAGACTCCAG[C/T]GGATGTATGGACAAC | 138151 |
| rs760628798 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136073150 | AAGAATTAATTGGCC[A/G]GGTATGGTGGCACGT | 138151 |
| rs760713638 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136080998 | CACCCCAAGCACATT[C/G]TGATTAACAGAGGTG | 138151 |
| rs760726545 | snp | C/T | 0.000347194 | 0.013171 | missense | NACC2 | GRCh38.p7 | 9:136011557 | CCGGCCTCCGGGCCG[C/T]GGCCGCCGGCGTCTG | 138151 |
| rs760728055 | in-del | -/AAAAAAAAAAAA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136066193 | GTGAAACCCCATCTC[-/AAAAAAAAAAAA]AGAAAGAAAGAAAAA | 138151 |
| rs760729364 | snp | C/G | | | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015964 | GGACCCTCGCGGGGC[C/G]GGGGGACTGGCAACT | 138151 |
| rs760766016 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136061056 | TGTCACATACTGGAA[C/T]GGACGGACGCCCCCT | 138151 |
| rs760782903 | snp | G/T | 2.45432e-05 | 0.003503 | missense, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136011994 | TTCATCTCGCTCTCC[G/T]TGAAGCTGGGGGCGA | 138151 |
| rs760791290 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136089804 | TATTAAAAAAAAATC[A/C]AATTATAGCACAAAT | 138151 |
| rs760805359 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007683 | AGCTCTGGATTCTGC[A/G]CTTAGGACTCGCTGC | 138151 |
| rs760870290 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136075635 | CGGGAGCAGAGCCTG[C/T]AGGGCCCCCTCAGGA | 138151 |
| rs760882601 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136089522 | CTCCTGTTAGCCCCT[C/T]CCCCAGCGCTGGGGG | 138151 |
| rs760945676 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136080405 | GGTATTAAAAACGTC[C/T]CTATTAAAAATACAA | 138151 |
| rs760959919 | snp | A/G | 7.08717e-05 | 0.00595238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012066 | AGCCACCTGCCTGCC[A/G]GGAGGCCCGCCCCTC | 138151 |
| rs761102710 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136055878 | AGGTCAATCGAAGGC[A/G]CTCCTGGAGCGTGAG | 138151 |
| rs761110170 | in-del | -/AGA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136025480 | AAACCAACAATTTAC[-/AGA]AGGACATCAGATCAG | 138151 |
| rs761228627 | snp | C/T | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096574 | ACCCCGCAGGGACTC[C/T]GGGCTCTCCCCACAG | 138151 |
| rs761264046 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136093572 | TAAGAAGTGACAAGT[A/G]ATATCTTGTTCCACT | 138151 |
| rs761264382 | snp | C/T | 1.66123e-05 | 0.00288199 | missense, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016331 | GATGGCAGCGGTATC[C/T]GATCTGGCTGATGAG | 138151 |
| rs761279066 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136070369 | AAAAATTAGCCGGGC[A/G]TGGTGGTGGGCGCCT | 138151 |
| rs761280512 | snp | A/G | 4.69473e-05 | 0.00484473 | missense | NACC2 | GRCh38.p7 | 9:136011742 | AGGTCAACATTCACG[A/G]CGTCAGTTCTCAGAG | 138151 |
| rs761314757 | snp | A/T | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012563 | TCCCAGAATCTTCCC[A/T]GAGCCTCGGCTGCCA | 138151 |
| rs761324169 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010711 | GGCGGCAGAGGGCAG[C/T]GTGTGCTACATCAGC | 138151 |
| rs761332799 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136092182 | TCTGGGAGGACCAAG[C/G]GCGTGCCCAGAGAGG | 138151 |
| rs761346092 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136092213 | GTGCCAGGAAAGGAA[C/T]GAAATGCTGGGGAGA | 138151 |
| rs761347730 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136029164 | GTTGCCTTTTCCGGG[C/T]CCACTCATGGCTGCC | 138151 |
| rs761359161 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136061361 | CTCACCACACAGAGG[C/T]ACAGCCCTCAGATAG | 138151 |
| rs761366565 | snp | C/T | 6.78956e-05 | 0.00582608 | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016231 | AATAAATGAGGACAT[C/T]TGCATACAATAGATG | 138151 |
| rs761381683 | snp | A/G | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013727 | CACCGTCCTGGGGCC[A/G]ACCGGCCACGGCTGA | 138151 |
| rs761405056 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136022088 | GGAGGCTGACCTGGC[A/T]CATGCCCTGCACTAT | 138151 |
| rs761431532 | snp | A/G | 8.08571e-05 | 0.00635783 | missense | NACC2 | GRCh38.p7 | 9:136011782 | TGGCGGCGTCGCCCC[A/G]CCGCTCGGCGTAGAT | 138151 |
| rs761471702 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074278 | ACACGGTGAAACCCC[A/G]TCTCTACTAATAAAA | 138151 |
| rs761496309 | snp | A/G | 5.22889e-05 | 0.0051129 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011728 | TGGCGGCGGCACTCA[A/G]GTCAACATTCACGGC | 138151 |
| rs761500544 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136071989 | GAGTCCGTAATCCCA[A/G]CACTTCGGGAGGCCC | 138151 |
| rs761562203 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136075522 | AGTTTCTCAAACAGA[A/T]CGCGCAGCTGGGGCC | 138151 |
| rs761638613 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136083200 | AGAGCCAGTGGCCAC[A/G]GGGCTCAGGGGAGCT | 138151 |
| rs761643992 | snp | A/G | 3.73937e-05 | 0.00432382 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013152 | CTCAGGCTGGGATCT[A/G]AACCCAGCCCCGGCC | 138151 |
| rs761689478 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136019279 | TCCCTCGTGGCCCCC[A/G]GAAGGGCCATTCAGA | 138151 |
| rs761711564 | in-del | -/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136018530 | CTCCCTCCCCAGGGA[-/C]CCCACTGGCCCAGGA | 138151 |
| rs761728486 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136084666 | GCAGCACCAGACAGC[C/T]AAGAGGCAAGTGGCC | 138151 |
| rs761729437 | in-del | -/CGCCAC | | | intron-variant | NACC2 | GRCh38.p7 | 9:136017117 | CCAGGCTGGCCGACA[-/CGCCAC]CGCCACCGCCACCGC | 138151 |
| rs761762875 | in-del | -/CAAAAAAAAAAA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136066192 | AGTGAAACCCCATCT[-/CAAAAAAAAAAA]AAGAAAGAAAGAAAA | 138151 |
| rs761781018 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136025162 | GAGGCCCTGGAAGGG[A/C]TACAGGCTACGGTGT | 138151 |
| rs761815237 | snp | A/G | 1.70883e-05 | 0.00292299 | synonymous-codon, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013224 | GTTCAGGACCCGGCT[A/G]TCCAGCGGCTTCCGG | 138151 |
| rs761818703 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074360 | CGGGAGGCTGAGGCA[A/G]GAGAATGGAGTGAAC | 138151 |
| rs761850439 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136088684 | GCATCGTGGTCTGGG[G/T]TCACTGAGACACAGG | 138151 |
| rs761934620 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136080263 | GCAGGGCCCCCGCAC[C/T]CATCTCTGTGCTCTC | 138151 |
| rs761949355 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136057881 | GGTGGGCAATGGGAG[A/G]CGGTCTGGAGCGTGC | 138151 |
| rs761991164 | snp | G/T | 1.69867e-05 | 0.00291429 | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016472 | ATGGGCATCTGGGGG[G/T]CCGGGCTGCTCTGTG | 138151 |
| rs761994754 | in-del | -/CC | | | intron-variant | NACC2 | GRCh38.p7 | 9:136090800 | CCCAGGGCCGGGCTG[-/CC]CTCGGGGCCCCGGTG | 138151 |
| rs762025449 | snp | A/G | 0.000100477 | 0.00708721 | missense | NACC2 | GRCh38.p7 | 9:136011901 | ATCTCCACGCCCTCC[A/G]GCAGCATGGACTTGA | 138151 |
| rs762113867 | snp | A/C | 2.46843e-05 | 0.00351306 | stop-gained, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136011986 | CGATCACGTTCATCT[A/C]GCTCTCCTTGAAGCT | 138151 |
| rs762167796 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136020122 | AGCATCACCGAACCA[C/T]GCACGTAAAAGTCAC | 138151 |
| rs762209647 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136093970 | CTGCCAGACGAAAAG[A/C]GGGGTGGGTGAGAAG | 138151 |
| rs762261266 | snp | A/G | | | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015209 | GAGGCTGGGATGACC[A/G]AGAGCATCTTCCTGG | 138151 |
| rs762284601 | in-del | -/AG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136042776 | CACACAGAGACACAC[-/AG]ACACACACACACATA | 138151 |
| rs762296997 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136063611 | TAAAAAGGCCGAGCA[C/T]GGTGGCTCACGCCTG | 138151 |
| rs762328696 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078618 | AGGCCATAAACCTGT[C/G]CGAGGCAAGAGGGGC | 138151 |
| rs762425128 | snp | C/G | 1.90119e-05 | 0.00308312 | synonymous-codon, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136013968 | GATGTAGACCCCAGA[C/G]CCTGCAGCCACCAAA | 138151 |
| rs762440693 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136021900 | GAAACTAAACTTGGG[G/T]GACAGAGAATCATTT | 138151 |
| rs762518973 | snp | A/G | 1.70682e-05 | 0.00292127 | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016223 | AATAAATAAATAAAT[A/G]AGGACATTTGCATAC | 138151 |
| rs762530437 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136021365 | CGTAAAAACACCGAC[A/G]CCAAGTGCCGGCGAG | 138151 |
| rs762599790 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136055731 | CAAATGCACAGCCAT[G/T]AAACACGTGGTAGAG | 138151 |
| rs762606198 | snp | A/C | | | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006216 | GTCCCGAAAAGGAGA[A/C]CCCCCGACCCTGGCA | 138151 |
| rs762621658 | in-del | -/AAAAA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136071543 | GTGAGACTCCATCTC[-/AAAAA]AAAAAAAAAAAAAAA | 138151 |
| rs762640494 | in-del | -/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024935 | GATCCTGAGAGCCGG[-/C]CTCAGGGTGCAATTT | 138151 |
| rs762654841 | snp | A/G | 1.80117e-05 | 0.00300092 | synonymous-codon, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136013956 | CTGGCCGCGTGTGAT[A/G]TAGACCCCAGAGCCT | 138151 |
| rs762695132 | snp | C/T | 0.000131596 | 0.00811054 | missense | NACC2 | GRCh38.p7 | 9:136011716 | CGAAGGCGGGGTTGG[C/T]GGCGGCACTCAGGTC | 138151 |
| rs762736640 | in-del | -/CTATA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136070382 | CGTGGTGGTGGGCGC[-/CTATA]CTATAATCCCAGCCA | 138151 |
| rs762787484 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012654 | TTTGCCTCACAAGGT[-/TT]TTTTTTTTTTTTTTT | 138151 |
| rs762798551 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136091248 | TGAAGGCAGAAAGGC[C/T]GGGCTGCCCACATTC | 138151 |
| rs762822426 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136029127 | CAGGCTGTCAGTTCC[G/T]CAGACTGGAGTGAGA | 138151 |
| rs762864293 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136060874 | GACTAGAGCCTTCTC[C/T]TCTGCATCCAGGAAG | 138151 |
| rs762917499 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136056917 | CAAATCCACAATTCC[A/G]TGTATCAGCCCTTCC | 138151 |
| rs762941856 | in-del | -/CCCAGCACTTTGGGAGGTCAAGGCTGGAAGATCACTTGAG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136064036 | ACTCAGGCCTATAAT[lengthTooLong]TCCAGGAGTTTGAGA | 138151 |
| rs763001327 | snp | A/G | 6.7382e-05 | 0.00580401 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012035 | GTACACTGTGAGGAC[A/G]GGGCGGCGTGAGCTC | 138151 |
| rs763032271 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136019092 | GGCTAAAAACACCCC[A/G]CCCCGAGTGGAAGCT | 138151 |
| rs763078824 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136087970 | TTCCGGGAGGTGACC[G/T]GGGGACTCTGCTGGG | 138151 |
| rs763098394 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136022289 | GTGCCCCACATGCAG[C/T]GGGCCTCGGGGAGAT | 138151 |
| rs763126842 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136087334 | CCCAGGAGATGGATA[A/C]CCTGCCCCCCTCCAA | 138151 |
| rs763176371 | snp | A/G | 1.67309e-05 | 0.00289226 | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016436 | TCTCTTGCACTGTGG[A/G]CCCAGAACCAACCTG | 138151 |
| rs763242651 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136028213 | GAAACTCCATCTCCA[-/A]AAAAAAAAAAAAAAA | 138151 |
| rs763338858 | snp | A/G/T | 0.000118301 | 0.00769003 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011846 | GAACTCGGGGTCGAG[A/G/T]GGCACGCTGGCGGCG | 138151 |
| rs763344027 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078062 | TAGGCATGAGCCACC[A/G]CGTCCGGCCCAATCA | 138151 |
| rs763399541 | snp | A/G | | | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015059 | TTCCTGCCATGGCCC[A/G]TCTCCTGCCCCACCA | 138151 |
| rs763409492 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009696 | GCCCAGTGGGAATGC[A/G]TCTAACCCACACCCT | 138151 |
| rs763411528 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031431 | CAAACTCTGCCTCCC[G/T]GGTTCGAGCAATTCT | 138151 |
| rs763429097 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008103 | TGCCCACAGCTTTGT[C/T]CACATTCAGGGGCAA | 138151 |
| rs763435175 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136070592 | GGCTGAGAGGAAAAT[G/T]TATAGCATTAATGGA | 138151 |
| rs763453389 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024992 | ACTACTAAGTAGCCA[C/T]GCATGCAGGCAGAGA | 138151 |
| rs763469504 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136080146 | CCCCACAAAAGCCAA[C/T]GGTTTGACCACAAGG | 138151 |
| rs763490832 | in-del | -/GCT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136090596 | GAGGGACCCCAGGCA[-/GCT]GCTCTGGCCAACAGC | 138151 |
| rs763499694 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010479 | TCCCCCAGTGGGAGA[C/T]GAGTGGTCCCTGGCC | 138151 |
| rs763535570 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136068290 | ATGACCTGAGGTCAG[A/G]AGTTCAAGACCAGCC | 138151 |
| rs763539467 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136057744 | CGGAGCGGCCGGGAG[A/G]GGAAGCACCCTCCTC | 138151 |
| rs763563271 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136088579 | GGTCCGGTGACCACC[A/G]CAGTCAGCCATGGTT | 138151 |
| rs763579786 | snp | A/C | 3.68759e-05 | 0.00429378 | synonymous-codon, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136013962 | GCGTGTGATGTAGAC[A/C]CCAGAGCCTGCAGCC | 138151 |
| rs763585766 | snp | A/G | 0.00108637 | 0.023281 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011681 | GACCGAGCCAGCCCC[A/G]TCCACCTCCTCGCCG | 138151 |
| rs763632352 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136060468 | TGTGGCAGCAGGCGC[C/T]TCTTTCCAGAAGACA | 138151 |
| rs763641322 | snp | A/G | 0.000146234 | 0.00854959 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013836 | CCGCAGCTCCATTGT[A/G]CCCTCCAGCACTCCT | 138151 |
| rs763661420 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136070464 | GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC | 138151 |
| rs763715218 | snp | C/T | 3.30967e-05 | 0.00406783 | missense | NACC2 | GRCh38.p7 | 9:136011587 | GGGGCCTGCTGGGGC[C/T]GCCCCCGCCCTGCTC | 138151 |
| rs763753314 | in-del | -/CACA | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007536 | AGACGCACAGACGTG[-/CACA]CACAGACACGCACAC | 138151 |
| rs763772865 | in-del | -/AG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024939 | CTGAGAGCCGGCCTC[-/AG]GGTGCAATTTCGGAA | 138151 |
| rs763801109 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136021374 | ACCGACGCCAAGTGC[C/T]GGCGAGGATGCGGGG | 138151 |
| rs763811452 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136075501 | CCGTCTCCTACATCG[C/T]GGTACAGTTTCTCAA | 138151 |
| rs763873665 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136077441 | TTGTTGATAAGTCGT[A/G]CTTCATTAAAATATT | 138151 |
| rs763935288 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136018103 | ACGTCCAGCAGGCTC[A/G]GGGCAGGCAGCTCCA | 138151 |
| rs764117075 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136027639 | GCAAAAGGGAAAAAA[A/C]AATCACAAATGACTA | 138151 |
| rs764154553 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136091388 | AGGAGACCTGAGCCC[A/G]GGGTTCTGGCTGCCA | 138151 |
| rs764163937 | snp | A/G | 1.66219e-05 | 0.00288283 | synonymous-codon, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016359 | GAGGCTGGCAGGTAG[A/G]GCCACGAGGTCGCGG | 138151 |
| rs764253749 | snp | A/T | 5.04147e-05 | 0.00502044 | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016453 | CCAGAACCAACCTGG[A/T]CAGATGGGCATCTGG | 138151 |
| rs764273096 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136057014 | TGGACAGCACAGCCC[C/T]CAGCCCCCACCCCCA | 138151 |
| rs764286597 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136066277 | GACTTATATCTAGAA[C/T]GTATAAATAATTCTG | 138151 |
| rs764359339 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008166 | TGACGACAGAGAACT[C/T]GGGTGGACAGACACA | 138151 |
| rs764369740 | in-del | -/TGCTCGAACACCTGTGCC | 3.65344e-05 | 0.00427386 | cds-indel | NACC2 | GRCh38.p7 | 9:136011801 | TCGGCGTAGATGCGT[-/TGCTCGAACACCTGTGCC]TGCTCGAACACCTGT | 138151 |
| rs764384359 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136030416 | AGATCGAGACCATCC[C/T]GGTGAACACAGTGAA | 138151 |
| rs764396241 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136062948 | TAAAATTATACGTTC[A/G]CAGGACATCCCAGAA | 138151 |
| rs764449731 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136093302 | GCAGCCTCATGCTTT[A/C]ATTGGAAAACAAAGG | 138151 |
| rs764461276 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136063567 | TCCTACCTGGGAAGG[G/T]TATGCACAAACAAGA | 138151 |
| rs764508454 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136025144 | AACACCAGGCTTTCA[C/G]CTGAGGCCCTGGAAG | 138151 |
| rs764513821 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136063152 | TCTGTCTCTCTCCTG[A/T]CAAACGTGTGGTTTG | 138151 |
| rs764548786 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136064154 | ATGAGCTGGGCGTTG[C/T]GTTGTGTACCTGTGG | 138151 |
| rs764551170 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136072049 | TTGAGACCAGCCTGG[C/T]CAACATGGTGAAACC | 138151 |
| rs764665835 | in-del | -/TA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024393 | TGTGAGGACAGAGGG[-/TA]TGTGTGAGGACAGAG | 138151 |
| rs764680546 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136021277 | TAGCACATGAAAAGA[C/T]ACTCAAGCATCCTTA | 138151 |
| rs764690567 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136068766 | AAAAGGAAATTTTAA[A/C]AATCGAGTGGCTCAC | 138151 |
| rs764697999 | snp | A/G | | | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014281 | CATGCTGCGGTCCCC[A/G]GCCTCAGCTCCCTCC | 138151 |
| rs764715897 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078102 | AATCACGAGGTTTGC[C/T]GTACTATCTTTAAAC | 138151 |
| rs764760811 | in-del | -/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024687 | CTATGCAAAAATAAA[-/T]ATATTTAACTTTTAA | 138151 |
| rs764774213 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136020540 | GCCCAGCAGAGCCTC[A/G]GCGGGGGTAGGAGGG | 138151 |
| rs764791272 | snp | C/T | 1.70443e-05 | 0.00291923 | synonymous-codon, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013257 | GGGGTCGCTGGTGGA[C/T]GAGCGGATGCCAGTC | 138151 |
| rs764824061 | snp | A/G | 0.000111468 | 0.0074647 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013823 | GAGCCAGAACCCTCC[A/G]CAGCTCCATTGTGCC | 138151 |
| rs764915657 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136076318 | GACTCTAAACACCCA[G/T]TTCCTCAAATGTTCT | 138151 |
| rs764990519 | snp | C/T | 0.000511154 | 0.0159786 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011567 | GGCCGCGGCCGCCGG[C/T]GTCTGGGGCCTGCTG | 138151 |
| rs765116290 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136026583 | GAGGGAGTGAGGTAA[C/T]GCAGGAGACAGTGAA | 138151 |
| rs765163736 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136060345 | GGCCCTGGAGCCGGC[A/T]GGGCTGCCTTTAAGC | 138151 |
| rs765170922 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136066120 | ATCACCTGAGCCCGG[A/G]AGGCAGAGGTTGCAA | 138151 |
| rs765256271 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136019078 | CACCGGGTGCTGCTG[A/G]CTAAAAACACCCCGC | 138151 |
| rs765300133 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136056010 | CCTTGCCCACCTCCG[C/T]GCAACGCCTTCCCTT | 138151 |
| rs765350783 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136064771 | AGCCAAAACAATATT[A/G]AAAAAGAGGAGCGAA | 138151 |
| rs765359680 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136086276 | AGCTGGGGACAGGAC[A/G]AAGGGCACATGCCCC | 138151 |
| rs765378458 | snp | C/G | 1.70711e-05 | 0.00292152 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012076 | CTGCCGGGAGGCCCG[C/G]CCCTCCCCAAGGCCA | 138151 |
| rs765387897 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136065469 | TACTAAAAATACAAA[A/G]GTCAGCCAGATGTGG | 138151 |
| rs765426041 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074562 | ATTTAAAATTATGTA[C/T]CATCCCTTCAATTAA | 138151 |
| rs765479115 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136070932 | GATAACGTGGAAATA[G/T]TAAGAACAATTTGAC | 138151 |
| rs765499165 | snp | C/G | 1.66142e-05 | 0.00288216 | missense, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016347 | GATCTGGCTGATGAG[C/G]CTGGCAGGTAGGGCC | 138151 |
| rs765504532 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136062923 | CCCTGTCTCTAAATA[A/G]GTAAATAAATAAAAT | 138151 |
| rs765505458 | snp | C/T | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136097025 | GTGTTTAGAAGATAG[C/T]GGATAAGCAGAAATC | 138151 |
| rs765590998 | snp | C/T | 7.30807e-05 | 0.00604442 | missense | NACC2 | GRCh38.p7 | 9:136011797 | GCCGCTCGGCGTAGA[C/T]GCGTTGCTCGAACAC | 138151 |
| rs765656983 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136056777 | AGCCAGGTCCCTAGG[C/T]GGCTTCTACCCCAGA | 138151 |
| rs765677937 | snp | C/T | | | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006452 | GCCCCTGGGGGACCA[C/T]TGGCCACCCCTGCCT | 138151 |
| rs765730794 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136028747 | CTCTTGGGGGCCTGG[C/G]AAGCCCCCCTGCCTG | 138151 |
| rs765743843 | snp | C/T | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013080 | CAGACCATGCTCGGC[C/T]CCCAGGGACGGAAGC | 138151 |
| rs765786676 | in-del | -/CAC | | | intron-variant | NACC2 | GRCh38.p7 | 9:136058637 | ACCGGGTACCATGCT[-/CAC]CACCTGAGTGACGAG | 138151 |
| rs765822874 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031486 | GGGATTACAGGTGTG[C/T]GCCACCACACCAGGT | 138151 |
| rs765946822 | snp | A/G | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013086 | ATGCTCGGCCCCCAG[A/G]GACGGAAGCTGCAGG | 138151 |
| rs765966407 | snp | A/G | 3.72523e-05 | 0.00431564 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013164 | TCTGAACCCAGCCCC[A/G]GCCCCACCCACCCGA | 138151 |
| rs765968470 | in-del | -/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136088900 | GGAAGGTTTCCCGGA[-/G]GAGACAGCAGGCAAT | 138151 |
| rs765996935 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136083452 | CTCTCCAAAATCCAC[A/G]TGCACCCCAAACTCG | 138151 |
| rs766010114 | in-del | -/AA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136026346 | AAAACTCCATCTCAA[-/AA]AAAAAAAAAAAAAAA | 138151 |
| rs766026966 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136059308 | CAAGGGGCACAGCCA[C/T]GCTTGGTGTCCAGAT | 138151 |
| rs766085755 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136082914 | GTGCATGGCCCTCTC[C/T]ACGCCTAGGATTTTG | 138151 |
| rs766138829 | snp | C/T | | | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014868 | ACCCCAGGTGTCCCA[C/T]CAGGGTCTGGGTGAG | 138151 |
| rs766172062 | snp | A/G | 9.17158e-05 | 0.00677122 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011558 | CGGCCTCCGGGCCGC[A/G]GCCGCCGGCGTCTGG | 138151 |
| rs766231038 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009374 | TCTAGGCTGGGTGGT[C/T]CTTAGTTCAGCAGAA | 138151 |
| rs766266919 | snp | C/G | 1.72728e-05 | 0.00293872 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011502 | CGGTCCCTCGCGCAG[C/G]CACCCAGCTCCGCTT | 138151 |
| rs766335400 | snp | A/G | 3.59202e-05 | 0.00423778 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011930 | GATCTTGGGCAGCCA[A/G]CGCTTGCGAACGCGG | 138151 |
| rs766342892 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136020295 | TGGGTTACTGATTGG[A/G]TTCTGAGGTGCTCCA | 138151 |
| rs766357889 | snp | C/T | | | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006396 | TGTTGTGTGGACAGC[C/T]GGCCTGGGGACGCCG | 138151 |
| rs766404531 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136017114 | ATAGCCAGGCTGGCC[A/G]ACACGCCACCGCCAC | 138151 |
| rs766440652 | in-del | -/AC | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096495 | CTCTGCGTCCAGAAC[-/AC]ACACACACACACACA | 138151 |
| rs766473940 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136094295 | CCAACTCCAGGGACC[C/G]GGCCTCGCGGCCTTC | 138151 |
| rs766486429 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136076201 | CAAATGATTTCCATC[C/T]AGTAGCAAAGAGAAC | 138151 |
| rs766500023 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136073165 | GGGTATGGTGGCACG[G/T]GCTTGTAGTCTCAGC | 138151 |
| rs766504570 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136064700 | CGGTTAATTTCTTTG[C/T]CAACATTGTCGAGCT | 138151 |
| rs766534773 | snp | C/G | 3.30978e-05 | 0.0040679 | synonymous-codon, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012002 | GCTCTCCTTGAAGCT[C/G]GGGGCGAAGTTCTGA | 138151 |
| rs766547318 | in-del | -/GGGTGACCCCTGTCCCCATTCAGAATGG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136089648 | GTTGGGGGAGGCCCT[-/GGGTGACCCCTGTCCCCATTCAGAATGG]GGGACCCCAGCCCCA | 138151 |
| rs766572651 | in-del | -/CA | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007480 | GCACACACACAGACG[-/CA]CACACGCACAGACAC | 138151 |
| rs766580988 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136026273 | TTGAACCCAGCGGGG[A/G]TGGAGGTTGCAGTGA | 138151 |
| rs766786235 | in-del | -/GG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136023115 | GGGAGGGAGGAGGGA[-/GG]GGGAGGAGGGAGGGA | 138151 |
| rs766833020 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136090002 | AAAAAAAAAAGAATA[A/G]ACTGCTGACAACAAA | 138151 |
| rs766849471 | snp | A/G | 4.98335e-05 | 0.00499142 | synonymous-codon, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016332 | ATGGCAGCGGTATCC[A/G]ATCTGGCTGATGAGG | 138151 |
| rs766862581 | in-del | -/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031422 | GCTCACTGCAAACTC[-/T]TGCCTCCCGGGTTCG | 138151 |
| rs766893804 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136055889 | AGGCGCTCCTGGAGC[A/G]TGAGAAGGTGTGGGG | 138151 |
| rs766944800 | in-del | -/AATA | | | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016203 | CAGAGCTCTCCAATA[-/AATA]AATAAATAAATAAAT | 138151 |
| rs766970546 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136061420 | CTGGAGGTCACCAGG[A/C]CCAGCTCCCAGGCTG | 138151 |
| rs766983862 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136065313 | AACATAGTGGGACCT[C/T]GTATCTACAAAAAAT | 138151 |
| rs766993274 | snp | A/C | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013730 | CGTCCTGGGGCCGAC[A/C]GGCCACGGCTGAAGT | 138151 |
| rs766998878 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136062736 | CCTGGGCAACATGGC[A/G]AAACCCCATCTCTAC | 138151 |
| rs767031555 | snp | C/G/T | 1.74393e-05 | 0.00295286 | missense | NACC2 | GRCh38.p7 | 9:136011692 | CCCCGTCCACCTCCT[C/G/T]GCCGGCGTCGAAGGC | 138151 |
| rs767104682 | snp | A/G | 1.68035e-05 | 0.00289853 | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016244 | ATTTGCATACAATAG[A/G]TGGGTGGGAGGCAGC | 138151 |
| rs767119401 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136079805 | CCTGTAAGATTTCAG[G/T]CCACCAGGACAGGCA | 138151 |
| rs767132479 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136069709 | GCATATTTCAGAGCA[A/C]ATAAAATTATCAGAG | 138151 |
| rs767203184 | snp | C/T | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012749 | CTCTTGGCCACCTGG[C/T]GCGAGCCGGCAGCAG | 138151 |
| rs767214415 | in-del | -/CA | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007409 | AGACACGCACGTGCA[-/CA]CACAGACGCGCGTGC | 138151 |
| rs767220475 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078806 | CCCCAGTAAGCACCC[C/G]CAGCGTGGTCCCCTC | 138151 |
| rs767232957 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136057075 | GGAGGGCTGGGAGGA[C/T]GCTCCATCCTCGGCA | 138151 |
| rs767368791 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136066384 | TATACACAAATGTCC[A/C]ATATACACACGCAAA | 138151 |
| rs767386545 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136070559 | CATACCAAAGTTTGT[A/G]GGACACCACTTAGGT | 138151 |
| rs767413634 | snp | A/C/T | 3.74302e-05 | 0.00432597 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013155 | AGGCTGGGATCTGAA[A/C/T]CCAGCCCCGGCCCCA | 138151 |
| rs767474392 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136072020 | AGGTGGGTGGATCAC[C/T]TGAGGTCAGGAGTTT | 138151 |
| rs767492843 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136082355 | CCTGTGCCACGTGCT[A/G]AGCCGGCGGATGGGC | 138151 |
| rs767560321 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136018286 | GCTGCCAAGGGGGCT[A/G]CTGGGGAGCAGCCTG | 138151 |
| rs767586735 | snp | C/T | 1.94026e-05 | 0.00311463 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011497 | GTACTCGGTCCCTCG[C/T]GCAGCCACCCAGCTC | 138151 |
| rs767604407 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136079616 | CAACCGAGGGCAGAA[A/G]AGAGGCCAGAGGCCC | 138151 |
| rs767649876 | snp | A/G | 1.7088e-05 | 0.00292296 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011852 | GGGGTCGAGGGGCAC[A/G]CTGGCGGCGGCGGAG | 138151 |
| rs767720161 | snp | A/G | 4.81406e-05 | 0.00490591 | missense | NACC2 | GRCh38.p7 | 9:136011904 | TCCACGCCCTCCGGC[A/G]GCATGGACTTGATCT | 138151 |
| rs767743810 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136088469 | GCTGCAAAGCCACAG[C/T]GGTCAGTCAGCAGGA | 138151 |
| rs767804688 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031684 | ACAAGAAAACACAGA[A/G]CTTTTCCTTAAAGCA | 138151 |
| rs767865825 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136032335 | GAAAACCACAGGACT[A/G]TTACAATGCTTAGAG | 138151 |
| rs767883288 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136084346 | GGCCTTCACCAAAGG[C/T]GGGTTGCTGGAGGGC | 138151 |
| rs767940499 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136087444 | CCTGGAGCTGGCAGA[C/T]TCCCACGGGGACCCC | 138151 |
| rs768007392 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136086564 | TCCCACCCCGGGCTC[C/T]ACTGTGACCCACACG | 138151 |
| rs768087637 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136079219 | AGACATCCTCCCAGG[A/G]TGGGAACTGCACTCT | 138151 |
| rs768088065 | snp | C/T | 3.8546e-05 | 0.00438994 | missense, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136013969 | ATGTAGACCCCAGAG[C/T]CTGCAGCCACCAAAC | 138151 |
| rs768114687 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136073117 | CATTTAACAAAGGAC[A/T]AATATCTAGGCTACA | 138151 |
| rs768115036 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136063666 | GGCGGGTGGATCACC[C/T]GAGGCCAGGAGTTCT | 138151 |
| rs768116528 | in-del | -/AC | | | intron-variant | NACC2 | GRCh38.p7 | 9:136042694 | GACATACACACACAG[-/AC]ACACACACAGACACA | 138151 |
| rs768138064 | in-del | -/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136089771 | TATTTTCTTAAAAGC[-/T]TTTTTTTTTTTCTTT | 138151 |
| rs768173461 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136087564 | CGCAGCTTCTGGGGC[C/T]GCCTGGGAGCCCTCT | 138151 |
| rs768193531 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136055850 | AGTTAGTTAAGTGAG[C/G]ACATCTCCTAAAAGG | 138151 |
| rs768202210 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031496 | GTGTGCGCCACCACA[A/C]CAGGTTAATTTTTGT | 138151 |
| rs768204715 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136072111 | GGCATGGTGATGTGC[A/G]CCTATAATCCCAGCC | 138151 |
| rs768206923 | in-del | -/AAAT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136072854 | AACTCCGTCTCAAAT[-/AAAT]AAATAAATAAATAAA | 138151 |
| rs768223968 | snp | C/T | 1.66263e-05 | 0.00288321 | missense, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016306 | GGGTCCCCTTCCGAG[C/T]AGAGCTTGGGATGGC | 138151 |
| rs768263511 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136086798 | CACGCCCATCCAGGT[G/T]CCATCCCAGCAGCGG | 138151 |
| rs768339919 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136019802 | AGAAGGAGCCCCCGC[C/T]GTACCTTCCAGGCCC | 138151 |
| rs768375247 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136018275 | GGCGTGGGGGGGCTG[C/T]CAAGGGGGCTGCTGG | 138151 |
| rs768376865 | snp | C/T | 6.11191e-05 | 0.00552773 | missense | NACC2 | GRCh38.p7 | 9:136011719 | AGGCGGGGTTGGCGG[C/T]GGCACTCAGGTCAAC | 138151 |
| rs768390486 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136062694 | TCAGCGGGGGTGGAC[C/T]GCTTGAGCCCAGCAG | 138151 |
| rs768423302 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136065844 | GGAAAGAAAACCCAG[A/G]TACATTAGACTTCCT | 138151 |
| rs768449125 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136092058 | ATTAGGGGGCGCCTC[A/G]GGGAGGCCGGTGTGG | 138151 |
| rs768506082 | snp | C/T | | | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014496 | GTCTCCCTATGTTGC[C/T]CAGACTGGTCTTGAA | 138151 |
| rs768588138 | snp | C/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009733 | CCCCAGGCCAGGGTG[C/G]AGCACATGGTCCTCC | 138151 |
| rs768665680 | snp | C/G | 1.70988e-05 | 0.00292389 | synonymous-codon, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013884 | AAAGAAGGTGGCCAG[C/G]AGCCTCCGCAGCAAG | 138151 |
| rs768862069 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136026950 | ATAACGTTTGTTGGC[C/T]GGGTGCAGTAGCTCA | 138151 |
| rs768900172 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136076030 | CATGAAGGTTACGTG[C/T]GGTCACGAAGAGATC | 138151 |
| rs768971029 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136049036 | TGCCCAGCAAAGCCT[A/G]AACAGTCTCCAGAGG | 138151 |
| rs768997125 | in-del | -/CT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136029325 | AGATGTTGAGGAGAC[-/CT]CTGCCTGCAGAGAGG | 138151 |
| rs769001544 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136081465 | CTCTCTGAGCGCGGG[A/G]TGCCCAGGAAGGCGG | 138151 |
| rs769027101 | snp | C/T | | | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015784 | AGTTGTAAAAATCTA[C/T]AAGGAGCTATGACGC | 138151 |
| rs769061257 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136059896 | CCTAACTCAATTGCA[G/T]CCAAGACCCACCCCG | 138151 |
| rs769073034 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136081201 | GCCACCCAGGCCGCT[A/G]GAAACCCAGGGGAAG | 138151 |
| rs769083696 | snp | C/T | 2.49336e-05 | 0.00353075 | missense, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136011977 | TGTCCGCGGCGATCA[C/T]GTTCATCTCGCTCTC | 138151 |
| rs769116980 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136025912 | AGAGCAAGACCATCT[C/T]GAAAACAAACAAAAA | 138151 |
| rs769157710 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136034705 | AAATAGTAACAATAA[A/G]TGAAGGAATAAAACC | 138151 |
| rs769175289 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136080674 | GGACACTCCACGGAG[C/T]TCTTGCTTATCTGAT | 138151 |
| rs769251092 | in-del | -/CGT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078949 | AGATGCCCTTAGCAC[-/CGT]CGTCGCCGGCATGAT | 138151 |
| rs769265273 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136080176 | GGCCTCCTGGCAGGG[A/C]CCTGTAGCCACGCCA | 138151 |
| rs769266927 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136089378 | CCCCTTGCTAGAAAC[C/T]TAGCACCCGCGAAGG | 138151 |
| rs769308954 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136083021 | CCCATTAGACATCTA[C/T]ACTCACATGAAAGCG | 138151 |
| rs769325978 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136064346 | GAAGAATGAACAAGC[A/C]CAGCAAGATTGCAAA | 138151 |
| rs769335254 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136032173 | TCCAAAAGGAGGGGA[A/G]GGAATATCAGCGAGC | 138151 |
| rs769396661 | snp | A/G | 0.000158625 | 0.00890435 | synonymous-codon, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136011963 | GGCGTTGGTGCACAT[A/G]TCCGCGGCGATCACG | 138151 |
| rs769408824 | snp | C/G | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096197 | CTCCCACAGCACGCT[C/G]AAGGGTCCTTGCAGG | 138151 |
| rs769409904 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008991 | CACGGGACATTGTGC[A/G]GGCCTGAACAGCAGT | 138151 |
| rs769538445 | snp | C/T | 3.59965e-05 | 0.00424228 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014020 | TCCCGGGCCATAGGG[C/T]CCGAAGAGGCGCACA | 138151 |
| rs769548655 | snp | A/G | 0.000105558 | 0.00726414 | synonymous-codon, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013947 | GTTCATCAGCTGGCC[A/G]CGTGTGATGTAGACC | 138151 |
| rs769570025 | in-del | -/AG | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007381 | CGTGCACACATACAC[-/AG]ACACGCGTGCAGAGA | 138151 |
| rs769606627 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078566 | CCCTGGAACCGTACC[C/T]GGATGCATAGACGGG | 138151 |
| rs769624660 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136056579 | CTGCCAGGGCCCTAA[G/T]GACTCTGTGGCAGAG | 138151 |
| rs769638581 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136022713 | CATCAACTACCAGTG[C/T]TGGCTGGGGCAGTGC | 138151 |
| rs769652692 | in-del | -/AAAACAAAAC | | | intron-variant | NACC2 | GRCh38.p7 | 9:136069549 | GTGAAACTCTGTCAA[-/AAAACAAAAC]AAAACAAAACAAAAC | 138151 |
| rs769659085 | snp | A/G | 5.08772e-05 | 0.00504341 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011708 | GCCGGCGTCGAAGGC[A/G]GGGTTGGCGGCGGCA | 138151 |
| rs769730167 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136021855 | AAAATGATTACATAC[C/T]GGTGATCCCATTTGT | 138151 |
| rs769744686 | in-del | -/CA | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010942 | CTGCACACACACGCA[-/CA]CACACACACACTCGT | 138151 |
| rs769752637 | snp | C/T | 3.42027e-05 | 0.00413523 | missense | NACC2 | GRCh38.p7 | 9:136011773 | CCACGATGGTGGCGG[C/T]GTCGCCCCGCCGCTC | 138151 |
| rs769752881 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136069274 | TCTATTGACTGGGCG[C/T]GGTGGCTCACACCTG | 138151 |
| rs769757842 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007230 | GCGATTCTGCATGAT[C/T]TTCCTTTCCTTTTCT | 138151 |
| rs769761948 | in-del | -/AAAAT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136033177 | TGAGACCCTGTCTCA[-/AAAAT]AAAATAAAATAAAAT | 138151 |
| rs769873658 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007094 | TTAGTTCTTTTTTTT[A/G]TCTGCTAAAAATAGT | 138151 |
| rs769889195 | snp | A/C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136092824 | GCCACCTGCTGCCCC[A/C/G]CTGTGGACTCCGACC | 138151 |
| rs769895404 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136075349 | CCTCCCTAGCTCCCC[C/T]GAGGCTGGCTGCTGC | 138151 |
| rs770058675 | snp | C/T | 1.72219e-05 | 0.00293439 | missense, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013208 | TCTTACATTTCACAG[C/T]GTTCAGGACCCGGCT | 138151 |
| rs770087523 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136030932 | CCTCGCAGTGCTGGG[A/C]TTACAGGAGTGAACC | 138151 |
| rs770121568 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136091968 | GGCCCCCACAGCCAA[A/G]GCCCAAACAACCTTC | 138151 |
| rs770136526 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136062493 | TAGCACTTCGTCTTC[A/G]GTGCCTAGGCCCAGA | 138151 |
| rs770171184 | snp | A/G | 2.06311e-05 | 0.00321172 | missense | NACC2 | GRCh38.p7 | 9:136011544 | GCATAGGTGCCCTCC[A/G]GCCTCCGGGCCGCGG | 138151 |
| rs770214275 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009646 | GGTCTCCTAGGGCCT[C/T]GCCACAGGGGTGGGC | 138151 |
| rs770237318 | snp | A/G | 6.13064e-05 | 0.0055362 | missense | NACC2 | GRCh38.p7 | 9:136011877 | GCGGAGCCCATGACC[A/G]TGCGGTACATCTCCA | 138151 |
| rs770302515 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009063 | CGGCTCCCTCCCTGT[C/T]CTGGCCAAGGGTGGG | 138151 |
| rs770305973 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136088540 | GACTCTTTCTCGGGG[A/G]CACTTGGGGCTCGTG | 138151 |
| rs770340949 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136093151 | ACACCTTGGTTCCCC[A/G]TTCCATCCCTCGGGC | 138151 |
| rs770419876 | in-del | -/AA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067269 | GGAAACTCTGTCTCA[-/AA]AAAAAAAAAAAAAAA | 138151 |
| rs770465837 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136063529 | CAGGACGAGCCTTTC[C/T]CTCCCATAAAGTATA | 138151 |
| rs770484345 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136081847 | GGGCAAGGCGGGGAG[A/G]GCAGCCAGCCCCCAC | 138151 |
| rs770487853 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136049603 | GCCCCGCTTCCCAGC[A/C]AGGTGGTGTGGGGCT | 138151 |
| rs770512196 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136060325 | TGGCTTTGGGATCAC[A/G]GGGAGGCCCTGGAGC | 138151 |
| rs770538755 | snp | A/C | | | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016530 | GGGGCCTGTGTTAGA[A/C]CCACTCTGCCCACCT | 138151 |
| rs770592946 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136088250 | GAGAATCTTCAATCT[A/G]GGAACTGTACCACTG | 138151 |
| rs770597309 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010725 | GCGTGTGCTACATCA[A/G]CTGTGCACGTCCCAC | 138151 |
| rs770627109 | snp | A/G | 5.70044e-05 | 0.00533844 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011837 | GGCAGGCGGGAACTC[A/G]GGGTCGAGGGGCACG | 138151 |
| rs770628840 | snp | A/G | | | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015552 | GAGGGAAGACCCCGA[A/G]ACGCTGCCCAAGGTA | 138151 |
| rs770718688 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136025539 | TAACAATTTTTAATG[C/T]GTACAAGAAATACAG | 138151 |
| rs770726423 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136021762 | CACATGACGTGTTAC[A/C]GCTTGGCTGTGAAAA | 138151 |
| rs770770265 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136032905 | CGCCTGTAATCCCAG[C/T]TACTCGGGAGGCTGA | 138151 |
| rs770784582 | snp | C/T | 1.7033e-05 | 0.00291826 | synonymous-codon, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013896 | CAGGAGCCTCCGCAG[C/T]AAGACCTTATGCTTC | 138151 |
| rs770796316 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078351 | GGGACAGGCACATCT[C/G]GGGGCAGGTTCTCCA | 138151 |
| rs770842535 | snp | C/T | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136095933 | CTGGACTGGGCCTGG[C/T]GCTGCCTTCAGGCCT | 138151 |
| rs770871255 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136028870 | GGCACTGTCATGACC[C/T]GGCCAGGTGTATGTG | 138151 |
| rs770889920 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136022007 | TGAATGAGGAAAGGT[C/T]GGGCTACACACCTGT | 138151 |
| rs770900690 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136075245 | GGAGGTGGCCAGGAC[G/T]CCAGGACACATTCTG | 138151 |
| rs770936995 | snp | A/G | 5.28332e-05 | 0.00513944 | missense | NACC2 | GRCh38.p7 | 9:136011646 | GCGGGCAGCGGCTCG[A/G]GGGCGGCCACCTCCT | 138151 |
| rs770973895 | in-del | -/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136064950 | CCAAGACCATTCAAT[-/G]GGGGAAAGAACAGTC | 138151 |
| rs770978573 | in-del | -/TGGG/TGTA/TGTGGA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024533 | GTGTGTGTGTGTGTG[-/TGGG/TGTA/TGTGGA]GACAGTGTGTGTGAG | 138151 |
| rs771002452 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136092986 | ACAGGGCTGGCTGAG[A/G]AAGGAACATGGGCTC | 138151 |
| rs771004089 | snp | G/T | 7.30273e-05 | 0.00604221 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012068 | CCACCTGCCTGCCGG[G/T]AGGCCCGCCCCTCCC | 138151 |
| rs771149049 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136066744 | CACAAATGTCTATCA[C/T]GGGCTGAATGGGTAA | 138151 |
| rs771218991 | snp | C/T | 1.74452e-05 | 0.00295335 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013192 | CGAGAGACCCCCAGG[C/T]TCTTACATTTCACAG | 138151 |
| rs771260814 | snp | G/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008973 | AAACGAGTGAGGAAG[G/T]GGCACGGGACATTGT | 138151 |
| rs771327029 | snp | A/G | 1.96134e-05 | 0.00313151 | missense | NACC2 | GRCh38.p7 | 9:136011533 | ACAAGGTCCCTGCAT[A/G]GGTGCCCTCCGGCCT | 138151 |
| rs771347057 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136018780 | AGCAAAACAACCCGG[C/G]TGGTATTTTAAAACA | 138151 |
| rs771364209 | snp | C/T | 3.8795e-05 | 0.00440409 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011491 | GCTCTAGTACTCGGT[C/T]CCTCGCGCAGCCACC | 138151 |
| rs771369822 | snp | C/G | 4.99214e-05 | 0.00499582 | synonymous-codon, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016389 | GCGGATGAGGACGCA[C/G]GAGCGGCTCTCCAGC | 138151 |
| rs771370905 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136056684 | ATGACGGGCCCCCTC[A/G]GACTATCACTGTCGC | 138151 |
| rs771458870 | snp | C/G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136066059 | CTAGCCGGGTGTGGT[C/G/T]GTGGGTGCCTGTAAC | 138151 |
| rs771481002 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136029644 | GGGGCTCTGCAGTTC[C/G]TGGCATCTCCAAGCT | 138151 |
| rs771578843 | snp | A/G | | | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014663 | TTGCCTTTCTGCTCC[A/G]TCCCAGATACCAGAG | 138151 |
| rs771648612 | snp | C/G | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012734 | CCACAGGAGGCTGTG[C/G]TCTTGGCCACCTGGT | 138151 |
| rs771657268 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136075084 | GGTTCTGCGTGAAAT[G/T]AGCCGATTCCACCTT | 138151 |
| rs771699533 | snp | C/T | 8.00544e-05 | 0.0063262 | missense | NACC2 | GRCh38.p7 | 9:136011784 | GCGGCGTCGCCCCGC[C/T]GCTCGGCGTAGATGC | 138151 |
| rs771765166 | snp | C/T | 1.66219e-05 | 0.00288283 | missense, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016324 | AGCTTGGGATGGCAG[C/T]GGTATCCGATCTGGC | 138151 |
| rs771765524 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024671 | AGTGAACACACATTA[G/T]CTATGCAAAAATAAA | 138151 |
| rs771779799 | snp | G/T | 4.98923e-05 | 0.00499436 | missense, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016379 | CGAGGTCGCGGCGGA[G/T]GAGGACGCAGGAGCG | 138151 |
| rs771809394 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031406 | GCAGTGGCACAATCT[C/T]GGCTCACTGCAAACT | 138151 |
| rs771812535 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136051278 | TCTCCCGTGCTCTCC[C/T]GGCTCGGACCAGACC | 138151 |
| rs771851191 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136057583 | TAAATAACGTAAGCT[C/T]GAAGAGCGTCTCCCT | 138151 |
| rs771856554 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007326 | AACCCTAAATGCTCC[A/G]GTGGTGACGTGCACG | 138151 |
| rs771888790 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136021909 | CTTGGGGGACAGAGA[A/G]TCATTTCCATTGTGG | 138151 |
| rs771918231 | in-del | -/TTT | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136097208 | AGCTCTGTTTATTCC[-/TTT]TTTTTTTTTTTTTTT | 138151 |
| rs771921992 | snp | A/G | | | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015448 | AGGCCACTCTCCCAT[A/G]AGGACCGAAGTCCCT | 138151 |
| rs771946911 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136064023 | GCCAGGCGTGGTAAC[C/T]CAGGCCTATAATCCC | 138151 |
| rs771951421 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136020146 | AAGTCACTGCAACGG[C/T]CCCTCTCACGTCCAC | 138151 |
| rs772075736 | snp | A/C | 1.70956e-05 | 0.00292361 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013329 | AAGGCAGGCAGGGTG[A/C]GGATGATGGGGAGGG | 138151 |
| rs772087549 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136068004 | GAAACATAGTAAAGG[C/T]TCAGTAAAAATATAG | 138151 |
| rs772093160 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136059959 | GTCCCCTCCTCAGGG[C/T]GCACGGGGAGCCGCC | 138151 |
| rs772102819 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136093788 | GCTCCAACGGTGGCC[A/G]GGAGAAGAAGGGGTG | 138151 |
| rs772177028 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136069707 | AAGCATATTTCAGAG[A/C]AAATAAAATTATCAG | 138151 |
| rs772182057 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136066824 | AGTACTGGGAGAGCA[C/T]GGATGAGCGCTACGC | 138151 |
| rs772184701 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136059053 | GTGCTGGGTCAGGGG[C/T]AGGGGAGAAGCGTGA | 138151 |
| rs772195023 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136076475 | GGGGTTCCACTCACA[C/T]GCGGGCACAGAGCAG | 138151 |
| rs772212070 | snp | A/G | 4.92514e-05 | 0.00496218 | synonymous-codon, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136011987 | GATCACGTTCATCTC[A/G]CTCTCCTTGAAGCTG | 138151 |
| rs772223427 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007641 | AGCAACATTCTGAAA[C/T]AGTAGTTACAGCTGA | 138151 |
| rs772293535 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136017654 | TGCCACGGTGGACAC[C/T]AGTCCGGCACTCCTC | 138151 |
| rs772328865 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067592 | CCTGTAATCCCAGCA[A/C]TTTGGGAAGCCAAGG | 138151 |
| rs772343752 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010504 | CTGGCCCTGGGCGGG[A/G]GAGCAGGGGGACGCA | 138151 |
| rs772357953 | in-del | -/T | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136097073 | GTGCCTATACGTATG[-/T]ACACCAACATATATT | 138151 |
| rs772394588 | in-del | -/GTGTGTGTGAGGACAGAGGGTGTGTGTGAGGACAGAGG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024212 | GTGAGGACAGAGTGT[lengthTooLong]GTGTGTGTGAGGACA | 138151 |
| rs772436764 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136020902 | CATCCGCACCCACAC[A/G]TGGCACCAAAACCAC | 138151 |
| rs772440496 | snp | A/G | | | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014263 | ACTCCAAGCTCTCCC[A/G]GCCATGCTGCGGTCC | 138151 |
| rs772482133 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136028783 | GCTCAGAAGTGCCTG[C/T]TCCTGCTGCCTGGCC | 138151 |
| rs772502404 | snp | C/T | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096369 | TCAGCCAAGGTCATT[C/T]CCTGGACAAATCATC | 138151 |
| rs772510076 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136065100 | GCTAAAACTATAAAA[C/T]TCTTACAAGAAAAGA | 138151 |
| rs772532771 | snp | C/G | 0.000116884 | 0.00764384 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012060 | GAGCTCAGCCACCTG[C/G]CTGCCGGGAGGCCCG | 138151 |
| rs772547055 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136017021 | CAGGGGCAAGGACAC[C/G]GGGGACTCAGTGCAT | 138151 |
| rs772570804 | snp | A/G | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012757 | CACCTGGTGCGAGCC[A/G]GCAGCAGTCAGCATC | 138151 |
| rs772574338 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136027088 | AGAAACAGCCGGTGT[A/G]GTGGCACATGCCTGT | 138151 |
| rs772576387 | snp | C/T | 1.93763e-05 | 0.00311252 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011474 | AGTAACGCATGCAAG[C/T]AGCTCTAGTACTCGG | 138151 |
| rs772681140 | in-del | -/CCCACTCTG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136060019 | GGGACACAGGGTGAC[-/CCCACTCTG]CCCACTCTGCCATGA | 138151 |
| rs772693604 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136079826 | AGGACAGGCAGCAGC[C/T]GGGGAAGTCTCAACT | 138151 |
| rs772698554 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136090734 | TGAGGCATGACTATG[C/T]GGAGGCTGATGCTCT | 138151 |
| rs772755992 | in-del | -/AAA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136026345 | CAAAACTCCATCTCA[-/AAA]AAAAAAAAAAAAAAA | 138151 |
| rs772815791 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136020918 | TGGCACCAAAACCAC[C/T]CTCCGTCTCAGCCTC | 138151 |
| rs772841098 | snp | G/T | 1.66349e-05 | 0.00288395 | stop-gained, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016326 | CTTGGGATGGCAGCG[G/T]TATCCGATCTGGCTG | 138151 |
| rs772855459 | snp | A/T | 3.91888e-05 | 0.00442638 | missense | NACC2 | GRCh38.p7 | 9:136011787 | GCGTCGCCCCGCCGC[A/T]CGGCGTAGATGCGTT | 138151 |
| rs772896751 | snp | C/T | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013736 | GGGGCCGACCGGCCA[C/T]GGCTGAAGTCAGGAA | 138151 |
| rs772972587 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024706 | TTTAACTTTTAAAAC[A/G]CCCCAGAGATTCCCA | 138151 |
| rs773063704 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136019060 | TATTTCTGCCTTGCC[A/G]TGCACCGGGTGCTGC | 138151 |
| rs773081706 | snp | C/T | 0.000368508 | 0.013569 | synonymous-codon, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013236 | GCTGTCCAGCGGCTT[C/T]CGGCTGGGGTCGCTG | 138151 |
| rs773127107 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067270 | GAAACTCTGTCTCAA[-/A]AAAAAAAAAAAAAAA | 138151 |
| rs773159958 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136020450 | TGACACCATCAGAGA[C/T]CACGCAGGCAGCCCC | 138151 |
| rs773167548 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031430 | GCAAACTCTGCCTCC[C/T]GGGTTCGAGCAATTC | 138151 |
| rs773223558 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136083878 | TCTTCTCAGACAGAC[A/G]ATGTCCACCAAGAAC | 138151 |
| rs773294875 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136026205 | AATTAGCCAGGTGTG[A/G]TGGTGCGCACCTGTA | 138151 |
| rs773330501 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136084852 | AGGACACCCCCTGTG[C/G]GACTCCACTCACATG | 138151 |
| rs773359608 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067600 | CCCAGCAATTTGGGA[A/G]GCCAAGGCGGGCAGA | 138151 |
| rs773513060 | snp | C/G | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096371 | AGCCAAGGTCATTCC[C/G]TGGACAAATCATCAG | 138151 |
| rs773521472 | snp | C/T | 2.45293e-05 | 0.00350201 | synonymous-codon, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136011993 | GTTCATCTCGCTCTC[C/T]TTGAAGCTGGGGGCG | 138151 |
| rs773529858 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136089694 | ACCCCAGCCCCAACA[C/G]AGTGAGTCATGTTCT | 138151 |
| rs773542242 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007658 | GTAGTTACAGCTGAG[A/G]ACAGCTACGAGCTCT | 138151 |
| rs773542491 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136085961 | GGGCACTGCACAGAA[C/T]GGCTCTGATGGGAGG | 138151 |
| rs773595833 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136017898 | CCTCCACCTGCCCGA[C/T]TGCACGAGGGCAGCC | 138151 |
| rs773727737 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136069577 | ACAAAACAAAACAAA[A/C]CAAAAAAAACACCTC | 138151 |
| rs773758242 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136023002 | AAGCCAGGAGGAAGA[A/T]AAATGAAGGCAGAGA | 138151 |
| rs773783983 | snp | C/T | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013694 | GACAGCCCCTCCCTC[C/T]CTCCCTGGGAGCCTC | 138151 |
| rs773826196 | in-del | -/C | 0.00018485 | 0.00961201 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013166 | TGAACCCAGCCCCGG[-/C]CCCACCCACCCGAGA | 138151 |
| rs773843162 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136079307 | GGAAGGGCTGCCTGG[C/T]ACCCAGCCACCTTCA | 138151 |
| rs773848074 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136056674 | GGTCTCTGGGATGAC[A/G]GGCCCCCTCGGACTA | 138151 |
| rs773895511 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136073321 | TGTGGTCCCAGCTAC[G/T]TGGGAGACTGAGGTG | 138151 |
| rs773903009 | snp | A/C/G | 3.35049e-05 | 0.00409286 | intron-variant, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016248 | GCATACAATAGATGG[A/C/G]TGGGAGGCAGCCTCA | 138151 |
| rs773929338 | snp | A/G | | | synonymous-codon | NACC2 | GRCh38.p7 | 9:136049856 | GGGCACCCCGTAGTA[A/G]GAGACACGGGGCAGT | 138151 |
| rs773935076 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078683 | TGGGAATGGCTGGGG[A/G]ACAGGTCAGGCACCT | 138151 |
| rs774001670 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136083285 | GCTTCACCCCAACCT[A/G]AGCCTAGGCACGCGG | 138151 |
| rs774020276 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136086811 | GTGCCATCCCAGCAG[C/T]GGCTGCTGTCTGTGC | 138151 |
| rs774094405 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136084591 | CACAGAATACACCAG[A/G]CTGGAAGAGCCCAGA | 138151 |
| rs774160820 | in-del | -/TTGT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024530 | TGTGTGTGTGTGTGT[-/TTGT]GTGGACAGTGTGTGT | 138151 |
| rs774170627 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136018312 | GCCTGAGGAGGGCAG[A/G]AGGCAGGGAGGGTCC | 138151 |
| rs774186619 | snp | C/T | 1.66228e-05 | 0.0028829 | synonymous-codon, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016311 | CCCTTCCGAGTAGAG[C/T]TTGGGATGGCAGCGG | 138151 |
| rs774291926 | snp | A/G | 0.00027859 | 0.011799 | missense | NACC2 | GRCh38.p7 | 9:136011556 | TCCGGCCTCCGGGCC[A/G]CGGCCGCCGGCGTCT | 138151 |
| rs774298668 | snp | A/C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136062735 | GCCTGGGCAACATGG[A/C/T]GAAACCCCATCTCTA | 138151 |
| rs774331806 | snp | A/G | | | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014541 | CAATCTTCCCACTTC[A/G]GCCTCCCAAAGTGCT | 138151 |
| rs774360983 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136092905 | CCTGCAAAGGGGATG[C/G]AGTGACCCCAAGGGG | 138151 |
| rs774393050 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136070365 | GCAAAAAAATTAGCC[A/G]GGCGTGGTGGTGGGC | 138151 |
| rs774416331 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009264 | CTTCCTCCCATCTCC[A/G]AGGAAGGCTTGGTCC | 138151 |
| rs774420984 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067569 | TGGGCCGGGCGCGGT[C/G]GCTCACGCCTGTAAT | 138151 |
| rs774464877 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136092106 | GAACTGGGGCCCAGT[A/G]GGGAGACAAGAGTAG | 138151 |
| rs774467500 | in-del | -/CGGA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136090733 | TGAGGCATGACTATG[-/CGGA]CGGAGGCTGATGCTC | 138151 |
| rs774506728 | snp | C/T | 2.74427e-05 | 0.00370414 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011639 | GCCATCGGCGGGCAG[C/T]GGCTCGGGGGCGGCC | 138151 |
| rs774548718 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024867 | TGGAGCAGCTGAGGC[A/G]GCAGGGCCTAAAGGC | 138151 |
| rs774603289 | snp | A/G | | | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015831 | AAAAGGTAAATTCCT[A/G]AGCGAGGCCCGGCCC | 138151 |
| rs774680007 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136093946 | ACAGGAGGGAAGGAG[A/G]TCAGGAGCCTGCCAG | 138151 |
| rs774694094 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136020102 | AAAACAGTGGGAATG[C/T]GCTTAGCATCACCGA | 138151 |
| rs774744937 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136022413 | CCACAACTTGCTTCC[C/T]AGCTCCCCGCCCAGG | 138151 |
| rs774748714 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136089384 | GCTAGAAACCTAGCA[C/T]CCGCGAAGGCCTGAC | 138151 |
| rs774765022 | snp | A/C | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136095855 | GAGGATACGGGAGCG[A/C]CCTTGGGCGAACGTC | 138151 |
| rs774784072 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031279 | TAAAGAGATGAGAAC[A/G]TCGGTATCAATGTTA | 138151 |
| rs774851388 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136073034 | TAAAAACTTTTGCTC[A/G]GCACAAGACACAGGT | 138151 |
| rs774859836 | snp | C/T | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012293 | CGCCAGCTGTGAGGC[C/T]CAGGCCTGTTTTTAA | 138151 |
| rs774877231 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136055689 | GGATTTAATTTCACC[A/G]ATCTAATAAGAGGTT | 138151 |
| rs774897007 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136058934 | GTGGATAGCGCTGCC[C/G]CTGGATGGGTAGCAG | 138151 |
| rs774906386 | in-del | -/AAA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136071545 | GAGACTCCATCTCAA[-/AAA]AAAAAAAAAAAAAAA | 138151 |
| rs774939416 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136080779 | ACACCCAGACCCCAG[C/T]GGAGTCACTGCAGAG | 138151 |
| rs774965277 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011411 | CATTTTTCTCAGGCA[A/G]CAGTAGCAGTTCAGT | 138151 |
| rs774968364 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136070332 | CCAAGATGGTGAAAC[C/T]CCGTCTCTACTAAAA | 138151 |
| rs774978742 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136086688 | CGCAGATGACAACGC[C/T]GACTCCTAGGAAAAC | 138151 |
| rs774996955 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136021324 | AAATCAAGCCATGTT[A/G]CGGTCCCACCTCCCA | 138151 |
| rs775041280 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136079707 | ACCAGAGCCCTGGAG[C/T]GTGGCTGCAGAAGCC | 138151 |
| rs775237061 | in-del | -/TGTT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136039035 | AAATAAAAGGCAGAC[-/TGTT]AGACTGCATAAAAAT | 138151 |
| rs775250253 | snp | A/G | 3.85356e-05 | 0.00438934 | missense | NACC2 | GRCh38.p7 | 9:136011670 | ACCTCCTGGATGACC[A/G]AGCCAGCCCCGTCCA | 138151 |
| rs775256535 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136081471 | GAGCGCGGGGTGCCC[A/G]GGAAGGCGGTGCCGG | 138151 |
| rs775258927 | snp | A/C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136064584 | CATCCATATTCATGG[A/C/G]ATGGGAAGACCTAAC | 138151 |
| rs775267093 | snp | A/G | 7.08893e-05 | 0.00595312 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011711 | GGCGTCGAAGGCGGG[A/G]TTGGCGGCGGCACTC | 138151 |
| rs775337815 | snp | A/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136068208 | CTTTTTTAAAAAAGT[A/T]ATTGTGTGGCTGGGC | 138151 |
| rs775386001 | snp | G/T | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012371 | GGGTCCCCCTTTCGG[G/T]AATAACACACCCCTC | 138151 |
| rs775433115 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136091133 | GCCTCTTGTTCTCCC[A/G]GGAGACTCCATGGCG | 138151 |
| rs775438301 | snp | A/C | | | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006205 | ATAAAACCAAGGTCC[A/C]GAAAAGGAGACCCCC | 138151 |
| rs775477660 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136021878 | CCATTTGTATGACAT[C/T]GTCCAGGAAACTAAA | 138151 |
| rs775493550 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136017092 | GCAACTCCATAAACA[A/C]TTGCCAATAGCCAGG | 138151 |
| rs775548118 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136018071 | CTGTGCAGAGGGAGG[A/G]GTGGGGTGGAACCTG | 138151 |
| rs775576477 | snp | A/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009149 | CCCCAGGGATGGTCA[A/T]ATTAAAGTGCAAATT | 138151 |
| rs775642053 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136066202 | CATCTCAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 138151 |
| rs775742373 | snp | A/G/T | 3.41268e-05 | 0.00413064 | missense | NACC2 | GRCh38.p7 | 9:136011845 | GGAACTCGGGGTCGA[A/G/T]GGGCACGCTGGCGGC | 138151 |
| rs775766074 | snp | G/T | 1.66893e-05 | 0.00288867 | missense, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016421 | GCACTGGCTCAGGCT[G/T]CTCTTGCACTGTGGG | 138151 |
| rs775806391 | snp | C/T | 2.08827e-05 | 0.00323124 | missense | NACC2 | GRCh38.p7 | 9:136011547 | TAGGTGCCCTCCGGC[C/T]TCCGGGCCGCGGCCG | 138151 |
| rs775807756 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136079409 | TGCAGAAGCCAATGC[A/G]TGGACTCCGGGGGCC | 138151 |
| rs775850647 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009665 | ACAGGGGTGGGCTTC[A/G]GGGCAGAAAGGAGCC | 138151 |
| rs775892739 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136027040 | TCAAGACCAGCCTGG[C/G]CAACATGGTGAAACC | 138151 |
| rs775911054 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136028921 | TGCCAGGCCCCTGCC[A/G]CCTTGGCCCCCTCTG | 138151 |
| rs775911365 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136071711 | AGGCTTATTATAAAC[C/T]ATAGTGATCAAGACT | 138151 |
| rs775956223 | in-del | -/GGGGACTCTGCTGGGAAGTTCCGGGAGGTGACCT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136087937 | CCAGTTTCCCACCCC[lengthTooLong]GGGGACTCTGCTGGG | 138151 |
| rs776001055 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136030951 | CAGGAGTGAACCACC[A/G]TGCCCGGCCAATACA | 138151 |
| rs776020672 | snp | C/G/T | 6.12051e-05 | 0.00553162 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011876 | GGCGGAGCCCATGAC[C/G/T]GTGCGGTACATCTCC | 138151 |
| rs776083604 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136093908 | CACCCTGCAGAATGC[G/T]GAGCTGAGTGTCCCA | 138151 |
| rs776085496 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136009559 | TATTTTTCTGGAGGG[C/T]AGGCATGTGCTGGGC | 138151 |
| rs776105952 | snp | C/T | 6.01124e-05 | 0.00548202 | missense | NACC2 | GRCh38.p7 | 9:136011880 | GAGCCCATGACCGTG[C/T]GGTACATCTCCACGC | 138151 |
| rs776115584 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136081931 | CCTGCAGCAGCACCC[C/T]GAAACCCCAGGGCTC | 138151 |
| rs776122234 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136056824 | GCATCAGCCATCAGA[A/G]CCGGCGGTAACTGCA | 138151 |
| rs776172444 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136087951 | CGGGGACTCTGCTGG[C/G]AAGTTCCGGGAGGTG | 138151 |
| rs776189272 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136091952 | GGTAACCTCGCTCCC[C/G]GGCCCCCACAGCCAA | 138151 |
| rs776199701 | in-del | -/CC | | | intron-variant | NACC2 | GRCh38.p7 | 9:136070013 | TGTTCTTTTCACGTG[-/CC]TGTGGAACATATGCC | 138151 |
| rs776204107 | snp | A/G | 1.70796e-05 | 0.00292224 | missense | NACC2 | GRCh38.p7 | 9:136011838 | GCAGGCGGGAACTCG[A/G]GGTCGAGGGGCACGC | 138151 |
| rs776224924 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136063536 | AGCCTTTCCCTCCCA[C/T]AAAGTATAGAGTTTT | 138151 |
| rs776359801 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136058379 | AGCCAGGGACCCGGG[-/A]TTCCCATCCTCAGGG | 138151 |
| rs776386910 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136089566 | AGGTGAACCCACCCT[C/T]GGGGTGCCCTCCCTC | 138151 |
| rs776401831 | snp | C/T | 3.71837e-05 | 0.00431167 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013820 | AAGGAGCCAGAACCC[C/T]CCGCAGCTCCATTGT | 138151 |
| rs776413634 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136025799 | ATGCACTTGTAGTCC[C/G]GGCTACTCAGGAAGT | 138151 |
| rs776475603 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136073893 | GGTCTGCCCAGAAGC[A/G]GGGTCAGCAGTAAGC | 138151 |
| rs776477960 | snp | A/G | 2.5288e-05 | 0.00355575 | missense | NACC2 | GRCh38.p7 | 9:136011649 | GGCAGCGGCTCGGGG[A/G]CGGCCACCTCCTGGA | 138151 |
| rs776493584 | snp | A/G | 2.34778e-05 | 0.00342612 | missense | NACC2 | GRCh38.p7 | 9:136011562 | CTCCGGGCCGCGGCC[A/G]CCGGCGTCTGGGGCC | 138151 |
| rs776556172 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136056046 | TACGGTGCAGGCTCC[A/G]GGAGGATTTGCTTTG | 138151 |
| rs776570125 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136068126 | AGAGAATGTGAAGGA[C/G]TGGGATATTACTATA | 138151 |
| rs776606575 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136021052 | CTAGAATTCATCAGA[A/C]TGAAAAACTTCCGAT | 138151 |
| rs776615683 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136032058 | GACCACAGAAGGGAT[A/G]ATTTCCCTCCCGCCA | 138151 |
| rs776664299 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136077803 | TAAAGTAATAAAAGG[C/T]AAGTGAAAGTAGTTT | 138151 |
| rs776666832 | in-del | -/GT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024093 | TGAGTGAGGGCCAGA[-/GT]GTGTGTGTGTGTGGG | 138151 |
| rs776691233 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136082109 | CCTGAACACGACCTG[A/C]CGGGGCCCTGGGTCA | 138151 |
| rs776713725 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136017171 | TCTGGGGCTGTTCCC[A/G]ACAAACCACTGCTGG | 138151 |
| rs776771870 | snp | G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136060170 | TCCTAGGGGCCAAAT[G/T]AAAGCTGCCACATAA | 138151 |
| rs776779291 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136081356 | ATGAAGCCAGCCACC[C/T]GCTGGGCTCCCCATG | 138151 |
| rs776790982 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136028903 | CTCAGGGCAGTGCTG[A/C]CATGCCAGGCCCCTG | 138151 |
| rs776839744 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136028622 | GAGCTGGCAGGAGCC[A/G]GGAACAGGTAGAAAT | 138151 |
| rs776852080 | snp | A/C/G/T | 0.000135791 | 0.00823895 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011495 | TAGTACTCGGTCCCT[A/C/G/T]GCGCAGCCACCCAGC | 138151 |
| rs776871678 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136090984 | GCGGGCCCAGGAGCT[C/T]GCGGCCGCCCATGGC | 138151 |
| rs776876720 | snp | A/G | 1.72922e-05 | 0.00294038 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012071 | CCTGCCTGCCGGGAG[A/G]CCCGCCCCTCCCCAA | 138151 |
| rs776928304 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010384 | CCGCTGCCTCCTGCC[C/T]GAGCGGAGTCCCCCG | 138151 |
| rs777016842 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008980 | TGAGGAAGGGGCACG[A/G]GACATTGTGCGGGCC | 138151 |
| rs777036441 | snp | C/T | 1.73339e-05 | 0.00294392 | splice-donor-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013198 | ACCCCCAGGCTCTTA[C/T]ATTTCACAGCGTTCA | 138151 |
| rs777048853 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136069185 | TGCTGGGATCATAGG[C/T]GTGAACTGCCGTGCC | 138151 |
| rs777067805 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136082954 | CCTCACTCCTGCCAG[A/G]TATCAGGGCGAGGGG | 138151 |
| rs777215151 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008334 | GGGGAAGAGGAAGGC[A/G]GGGCAGGAGAGGCGG | 138151 |
| rs777231402 | snp | A/G | 1.946e-05 | 0.00311923 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011521 | CCAGCTCCGCTTACA[A/G]GGTCCCTGCATAGGT | 138151 |
| rs777241121 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136065391 | TTGGGAGGCCGAGGC[A/G]GGCAGATCACTTGAG | 138151 |
| rs777276264 | snp | A/G | | | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136015505 | GGCAACCCTCAGGCA[A/G]TGGCTCACACCTGAG | 138151 |
| rs777401667 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010211 | ATCCCTAACCCTCTG[C/T]CCCCTACCAGTGCCC | 138151 |
| rs777453209 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136025464 | ACAAAACAACAAAAC[A/C]AAACCAACAATTTAC | 138151 |
| rs777455202 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136059637 | GAACCTGAGCAGGCC[A/G]CAGGGCCGGGACTTC | 138151 |
| rs777487033 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136094793 | CTTCCCCACCCGGAG[A/G]GCTGGATCGGCCAGT | 138151 |
| rs777508734 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136088115 | GTCGGGCTTGTACGG[C/T]CGCCAGGTGGACAGT | 138151 |
| rs777545372 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136058770 | CAACTCACACAGCAC[C/T]AGAGATTCGGAATAG | 138151 |
| rs777557085 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136032770 | GGGCATGGTGGCTCA[C/T]GCCTGTAATCCGCCA | 138151 |
| rs777598365 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136075097 | ATGAGCCGATTCCAC[C/T]TTGTCCTCAATGGCG | 138151 |
| rs777604854 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136023242 | CATGGGTGCAGCTGC[A/G]GGGGAAGATGTGGGG | 138151 |
| rs777620477 | snp | C/T | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136097160 | GTATGTACACCTTAC[C/T]GCATTTAACGTTCAC | 138151 |
| rs777634880 | in-del | -/CACA | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007348 | ACGTGCACGCGCGTG[-/CACA]CACACAGACACACGC | 138151 |
| rs777654144 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136064057 | ACTTTGGGAGGTCAA[A/G]GCTGGAAGATCACTT | 138151 |
| rs777658233 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136073720 | GAAAAGCAGCTGCGT[A/G]TGTGCTACAATTTTG | 138151 |
| rs777684386 | snp | C/T | 0.000129299 | 0.00803946 | missense | NACC2 | GRCh38.p7 | 9:136011863 | GCACGCTGGCGGCGG[C/T]GGAGCCCATGACCGT | 138151 |
| rs777704575 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136084836 | ATGAGCCAGTCACAC[A/G]AGGACACCCCCTGTG | 138151 |
| rs777719020 | snp | C/T | 3.19412e-05 | 0.0039962 | missense | NACC2 | GRCh38.p7 | 9:136011941 | GCCAGCGCTTGCGAA[C/T]GCGGCGGGCGTTGGT | 138151 |
| rs777748410 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136072482 | CCCAGAAGGCAGAGA[C/T]TGCAGTGAGCCAAGA | 138151 |
| rs777819800 | snp | C/T | 1.66352e-05 | 0.00288398 | synonymous-codon, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016296 | CTTCTCCCCGGGGTC[C/T]CCTTCCGAGTAGAGC | 138151 |
| rs777821979 | snp | G/T | 1.69908e-05 | 0.00291463 | missense | NACC2 | GRCh38.p7 | 9:136011706 | TCGCCGGCGTCGAAG[G/T]CGGGGTTGGCGGCGG | 138151 |
| rs777924546 | snp | A/C | 1.6838e-05 | 0.0029015 | stop-gained | NACC2 | GRCh38.p7 | 9:136011806 | CGTAGATGCGTTGCT[A/C]GAACACCTGTGCCGC | 138151 |
| rs777971070 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136032146 | AGAAGGATCCATGGC[C/T]CTGGAGAGCCGTCCA | 138151 |
| rs778040250 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136021725 | TGCAATGGGCATGCA[C/G]ATAAAGACACTGTGA | 138151 |
| rs778060017 | in-del | -/ATGT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024503 | GTGTGTGAGGACAGA[-/ATGT]GTGTGTGTGTGTGTG | 138151 |
| rs778105259 | snp | C/T | 1.69977e-05 | 0.00291523 | missense, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013261 | TCGCTGGTGGACGAG[C/T]GGATGCCAGTCCCGC | 138151 |
| rs778106172 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136078300 | GACGCCAGAATTCCA[C/T]GAAGCTCAGTCCCTC | 138151 |
| rs778162876 | in-del | -/AAT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136017813 | CTTCACTAGGGAATC[-/AAT]CCCACTGCCCTGGGC | 138151 |
| rs778185340 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136082762 | CCCCCTCTCCCCGGC[A/G]GGTGGGGCTGGCTCT | 138151 |
| rs778186223 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136077708 | TCACCCGGGAAATGC[A/G]AGGGGACCCCAAGGA | 138151 |
| rs778192077 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136086342 | GGGGTGGGGGTGCCT[A/C]TGTTTTCCTGCATCA | 138151 |
| rs778200827 | snp | C/G | 1.93924e-05 | 0.00311381 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011482 | ATGCAAGCAGCTCTA[C/G]TACTCGGTCCCTCGC | 138151 |
| rs778205126 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136092646 | TCAGCCTGGGCCACT[A/G]AGGCAGGGACATGTG | 138151 |
| rs778216406 | snp | A/G | 0.000124121 | 0.00787688 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013182 | CCCACCCACCCGAGA[A/G]ACCCCCAGGCTCTTA | 138151 |
| rs778229608 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136028793 | GCCTGCTCCTGCTGC[C/T]TGGCCCTCTCCTCAC | 138151 |
| rs778290803 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136091683 | CCGTAAACAGCAAAC[A/G]CAGGAAGGCCACAGC | 138151 |
| rs778332179 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136006778 | GCACAAAAACAGAGT[A/G]AGGGCTCAGGAAAAC | 138151 |
| rs778368786 | snp | A/C | 1.80523e-05 | 0.0030043 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013176 | CCCGGCCCCACCCAC[A/C]CGAGAGACCCCCAGG | 138151 |
| rs778424156 | snp | A/G | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008853 | CGGCCTGGCCCGCCC[A/G]GGGCGCAGGGAGAGC | 138151 |
| rs778441542 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136061839 | TACGAAAAGTTGGTG[A/G]CCGGGCGCGGTGGCT | 138151 |
| rs778474896 | snp | C/T | 1.94294e-05 | 0.00311678 | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136011513 | GCAGCCACCCAGCTC[C/T]GCTTACAAGGTCCCT | 138151 |
| rs778494953 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136058435 | TGCTCAGGAGGGGGC[C/T]CCGGAGGCTCCCCAG | 138151 |
| rs778508108 | snp | A/C | | | downstream-variant-500B | NACC2 | GRCh38.p7 | 9:136006509 | TGTCTCCCCCAAACC[A/C]CACAGGGCCAAGCCA | 138151 |
| rs778528179 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136019551 | CTCAGCATGGTGACA[C/T]CTGGGAACAGCTCAT | 138151 |
| rs778584889 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136057376 | CTCGAAGGGTGGGGA[A/G]GGACAGCTGGGGCTG | 138151 |
| rs778637297 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136021819 | GATGGATCTCAAATC[A/G]TGCTGTTACACAGAA | 138151 |
| rs778694384 | in-del | -/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136021651 | AAGACAGCCTGCACA[-/G]GAACGCTTATCCCGT | 138151 |
| rs778702051 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136025325 | CACCTGTTTTCACAC[A/G]ATGTCCGGCCGTCCA | 138151 |
| rs778717189 | snp | C/T | 1.66319e-05 | 0.00288369 | | | GRCh38.p7 | 9:136016302 | CCCGGGGTCCCCTTC[C/T]GAGTAGAGCTTGGGA | 138151 |
| rs778804669 | in-del | -/C | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096184 | TAAGCCAGCCTCACT[-/C]CCACAGCACGCTCAA | 138151 |
| rs778837970 | snp | A/G | 1.66275e-05 | 0.00288331 | missense, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016373 | GGGCCACGAGGTCGC[A/G]GCGGATGAGGACGCA | 138151 |
| rs778848186 | in-del | -/T | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136097062 | CAATTTCTGTGTGCC[-/T]TATACGTATGTACAC | 138151 |
| rs778858211 | snp | A/G | 6.41581e-05 | 0.00566347 | missense | NACC2 | GRCh38.p7 | 9:136011859 | AGGGGCACGCTGGCG[A/G]CGGCGGAGCCCATGA | 138151 |
| rs778859454 | snp | C/T | 2.62988e-05 | 0.00362612 | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014002 | AAAAAGGGCTCGTGG[C/T]CTTCCCGGGCCATAG | 138151 |
| rs778888010 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136032695 | TGAGATCAGGAGTTC[A/G]AGACCAGCCCATCCA | 138151 |
| rs779031306 | in-del | -/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136082661 | GCCTCCACGGACCTG[-/C]CCTCCCAAGAAGCAC | 138151 |
| rs779075499 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136021657 | GCCTGCACAGGAACG[C/T]TTATCCCGTCTCTAC | 138151 |
| rs779113994 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136069539 | GGGTGAAAGAGTGAA[A/G]CTCTGTCAAAAAACA | 138151 |
| rs779125321 | in-del | -/TTT | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012653 | ATTTGCCTCACAAGG[-/TTT]TTTTTTTTTTTTTTT | 138151 |
| rs779274514 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136060703 | TGCAGGACGCTCCCA[A/G]GTGAAGAGCGTGAGA | 138151 |
| rs779308256 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136067878 | GGTACAGCCTAACTG[C/T]GGTTAGGCTATATGG | 138151 |
| rs779620527 | snp | C/T | 0.000359454 | 0.0134014 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012050 | GGGGCGGCGTGAGCT[C/T]AGCCACCTGCCTGCC | 138151 |
| rs779653679 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136018460 | AAGGCAGCAGGTGTT[A/C]CACTCCTGAGAACCA | 138151 |
| rs779702181 | in-del | -/C | 1.78039e-05 | 0.00298356 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013852 | CCTCCAGCACTCCTG[-/C]CCCCGACCTACCTGT | 138151 |
| rs779727559 | snp | A/G | 6.65159e-05 | 0.00576659 | missense, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016303 | CCGGGGTCCCCTTCC[A/G]AGTAGAGCTTGGGAT | 138151 |
| rs779741475 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136029362 | CCACTCCAGGGTCTC[C/T]TTGAGAGCTGTACTG | 138151 |
| rs779767108 | snp | A/C | | | intron-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014480 | AGTTAATTTTGATGA[A/C]GTCTCCCTATGTTGC | 138151 |
| rs779805424 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136079137 | TATGTCTGTGCGTCC[C/T]GTCCTTAACAAGAGA | 138151 |
| rs779810814 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136075076 | ACGCTCTTGGTTCTG[C/T]GTGAAATGAGCCGAT | 138151 |
| rs779900721 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136081749 | GCACCATCCCCACCA[A/G]GTGGCGGCAGCAGCT | 138151 |
| rs779903083 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136079700 | CAGGGTCACCAGAGC[C/T]CTGGAGCGTGGCTGC | 138151 |
| rs779916515 | snp | A/G | 1.70909e-05 | 0.00292321 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011774 | CACGATGGTGGCGGC[A/G]TCGCCCCGCCGCTCG | 138151 |
| rs779931922 | in-del | -/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136058716 | ACCTGTACACGTATC[-/T]TCTGAATCGAAAATA | 138151 |
| rs779945143 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136022766 | CAGAAACGACTTCCA[C/T]GCTGTACTTGGTGGG | 138151 |
| rs780002314 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136091224 | CCCCCAGGCCAGCCC[C/T]AGCCGGCATGAAGGC | 138151 |
| rs780003174 | snp | C/T | 3.32491e-05 | 0.00407719 | missense, downstream-variant-500B | NACC2, LOC105376322 | GRCh38.p7 | 9:136016370 | GTAGGGCCACGAGGT[C/T]GCGGCGGATGAGGAC | 138151 |
| rs780003963 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136083698 | GGGGGCCCCGAGACA[C/T]TGTGGCCTGGGGCTT | 138151 |
| rs780004279 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136087524 | ACAGAGCCAGTCCTC[A/G]CAGGGCCCGGCTGGG | 138151 |
| rs780032206 | in-del | -/TGTGTGT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024526 | GTGTGTGTGTGTGTG[-/TGTGTGT]GGACAGTGTGTGTGA | 138151 |
| rs780098827 | snp | A/G | 1.7336e-05 | 0.00294409 | synonymous-codon, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013866 | TGCCCCGACCTACCT[A/G]TCAAAGAAGGTGGCC | 138151 |
| rs780151927 | in-del | -/CA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136066192 | AGTGAAACCCCATCT[-/CA]AAAAAAAAAAAAGAA | 138151 |
| rs780221211 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136031879 | GGCTCTGCATTCCCA[C/T]CTCCTCTAACTGTGA | 138151 |
| rs780266546 | snp | C/T | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136013690 | GAAAGACAGCCCCTC[C/T]CTCCCTCCCTGGGAG | 138151 |
| rs780361596 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136086356 | TCTGTTTTCCTGCAT[A/C]ATCAGGAGCCTGGTG | 138151 |
| rs780380241 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136071221 | CAGCCTGGGAGACAG[A/G]GCAAGACTACGTCTC | 138151 |
| rs780393663 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136063134 | GTGGGCCAGGTCTGT[C/T]GATCTGTCTCTCTCC | 138151 |
| rs780458970 | in-del | -/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136080928 | CCGCTCGAGTAGGTC[-/G]GGGGGGACACAGGCC | 138151 |
| rs780482338 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136058852 | CAAAAGTCCTTGGCA[A/G]AGCTCAAGCCATGGA | 138151 |
| rs780509140 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136010331 | AGACGGGGAGCCCAG[C/T]ACCGGGAGGACCGAC | 138151 |
| rs780527656 | snp | C/G/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136080464 | GCAATCCCAGCTACT[C/G/T]GGGAGGCTGAGACAG | 138151 |
| rs780536659 | snp | C/T | 0.000339041 | 0.0130156 | missense | NACC2 | GRCh38.p7 | 9:136011629 | GGGGGCTCTGGCCAT[C/T]GGCGGGCAGCGGCTC | 138151 |
| rs780568662 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136073167 | GTATGGTGGCACGTG[A/C]TTGTAGTCTCAGCTA | 138151 |
| rs780598885 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136020658 | AATATACAACTTAAA[C/T]GCAAATGGACAGAAC | 138151 |
| rs780624769 | snp | C/T | 0.00119342 | 0.0243985 | missense | NACC2 | GRCh38.p7 | 9:136011695 | CGTCCACCTCCTCGC[C/T]GGCGTCGAAGGCGGG | 138151 |
| rs780740210 | snp | A/G | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136095998 | ATTCCGGCACCGGCC[A/G]CGCAGCTCTCCATCT | 138151 |
| rs780766846 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136073892 | TGGTCTGCCCAGAAG[C/G]AGGGTCAGCAGTAAG | 138151 |
| rs780774457 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136059855 | GAGTCCCTACCTCGC[C/T]GTCAAAAGGACCCCA | 138151 |
| rs780789333 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136027915 | TTTGAAAAGACAAAT[A/G]TAATGGAAACTCTCT | 138151 |
| rs780794293 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136017373 | CTCTAGAGCGTTCAT[A/G]GAGGGCCAGGGCTGA | 138151 |
| rs780858805 | snp | A/G | 5.74119e-05 | 0.00535748 | synonymous-codon | NACC2 | GRCh38.p7 | 9:136011951 | GCGAACGCGGCGGGC[A/G]TTGGTGCACATGTCC | 138151 |
| rs780924701 | in-del | -/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007161 | AATCGTGTACGATGC[-/T]AACAATGGAAGCGAC | 138151 |
| rs780946226 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136086451 | CCCAGGTCTGCGAGC[A/G]GCTGGGCTTCCCTGA | 138151 |
| rs780949483 | in-del | -/GGA | 7.08717e-05 | 0.00595238 | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012066 | GCCACCTGCCTGCCG[-/GGA]GGAGGCCCGCCCCTC | 138151 |
| rs780953619 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136081143 | TCCCAGAGGAGGAAG[C/G]CCAGACCAAACGGAC | 138151 |
| rs781043643 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136090343 | TCCCTCCAAGACCGC[C/T]GCAGAAGAACCAAGG | 138151 |
| rs781047513 | in-del | -/GGTCAGGAGTT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136061906 | GGGCGGATCACCTGA[-/GGTCAGGAGTT]CGAGACTAGCCTGGC | 138151 |
| rs781064745 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136029790 | CTGCAGCCAGTGTGC[C/G]TGGCTGTGCACAGTG | 138151 |
| rs781154352 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136062290 | ACCCAGCAGTCACTC[A/G]CTTACCTAGGAGGAT | 138151 |
| rs781227410 | snp | A/G | 3.42366e-05 | 0.00413729 | missense | NACC2 | GRCh38.p7 | 9:136011820 | TCGAACACCTGTGCC[A/G]CGGCAGGCGGGAACT | 138151 |
| rs781303648 | in-del | -/GTGA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136068097 | TGGGCATTGCTCTGG[-/GTGA]GTGAGTAGTGAGAGA | 138151 |
| rs781356635 | in-del | -/AACA | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096493 | CAGCTCTGCGTCCAG[-/AACA]CACACACACACACAC | 138151 |
| rs781382111 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136023851 | CTGAGAAGGACGACC[A/G]GGACACTAAGGACAA | 138151 |
| rs781384760 | in-del | -/TGTG/TGTGTG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024507 | TGAGGACAGAATGTG[-/TGTG/TGTGTG]TGTGTGTGTGTGTGT | 138151 |
| rs781409475 | in-del | -/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136094272 | GGGAGTGGAACGGCC[-/T]TGGGAGGCCAACTCC | 138151 |
| rs781446471 | in-del | -/GAAAGGAAGGAAG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136041001 | AGGAAAGGAAGGAAA[-/GAAAGGAAGGAAG]GAAAGGAAGGAAGGA | 138151 |
| rs781491160 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136068318 | GCCTGGTCAACATGG[C/T]AAAACCCTGTCTCTA | 138151 |
| rs781543534 | in-del | -/AAAA | | | intron-variant | NACC2 | GRCh38.p7 | 9:136026344 | GCAAAACTCCATCTC[-/AAAA]AAAAAAAAAAAAAAA | 138151 |
| rs781581129 | in-del | -/CA | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007539 | GCACAGACGTGCACA[-/CA]CACAGACACGCACAC | 138151 |
| rs781605664 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136093013 | GCTCTGCCCCACTGA[C/T]GGTGGCTGGGGCCAC | 138151 |
| rs781629246 | snp | G/T | 2.0255e-05 | 0.00318231 | missense | NACC2 | GRCh38.p7 | 9:136011541 | CCTGCATAGGTGCCC[G/T]CCGGCCTCCGGGCCG | 138151 |
| rs781635636 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136083598 | CCTGTGAAGAGCGCC[A/G]TGCAGAGGCCAGGCC | 138151 |
| rs781653855 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136049516 | ACCTCCTCCAGGCTT[A/G]GTGGGGGGCTCCCCT | 138151 |
| rs781671944 | snp | A/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136030559 | AGCTTGCAGTGAGCC[A/G]AGACTGCGCCACTGC | 138151 |
| rs781765934 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136019587 | GCAATGAGCTAACTG[C/T]ATGGAGGTGAACAAC | 138151 |
| rs796163838 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136035581 | GGGAAAAAACCACTG[C/T]TCTAAAGAACAATAT | 138151 |
| rs796200581 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136063883 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAC | 138151 |
| rs796234014 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136066963 | AAAAAAAAAAAAAAA[-/A]GATTTAGCTGGACGC | 138151 |
| rs796257245 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136006952 | AACCCCTAAACAGAC[C/T]CTTTAAAACAACCGT | 138151 |
| rs796282353 | in-del | -/AA | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096493 | CAGCTCTGCGTCCAG[-/AA]CACACACACACACAC | 138151 |
| rs796336302 | multinucleotide-polymorphism | CA/TG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136081015 | ATTAACAGAGGTGAT[CA/TG]AGGAGGAAGTTTTCA | 138151 |
| rs796377665 | in-del | -/AT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074288 | ACCCCGTCTCTACTA[-/AT]AAAATACAAAAAAAT | 138151 |
| rs796399142 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136088255 | TCTTCAATCTGGGAA[C/T]TGTACCACTGCCCAC | 138151 |
| rs796412348 | in-del | -/CA | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007460 | ACACACACGCGCACA[-/CA]GACGCACACACACAG | 138151 |
| rs796414294 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136028229 | AAAAAAAAAAAAAAA[-/A]TTGACACCATTAAGG | 138151 |
| rs796458597 | in-del | A/GC | | | upstream-variant-2KB | NACC2 | GRCh38.p7 | 9:136096073 | GGCACGGAAATAAAA[A/GC]GGCCACACACCCGGA | 138151 |
| rs796459067 | in-del | -/GA | | | intron-variant, nc-transcript-variant | NACC2, LOC105376322 | GRCh38.p7 | 9:136014995 | TGTCCTGAAGGACAC[-/GA]TGTCCAGGTGCGCCT | 138151 |
| rs796492752 | snp | A/T | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012599 | CACTTGGGGACTGTA[A/T]TTCCTGGCTGCAAAG | 138151 |
| rs796524893 | in-del | -/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136058381 | CCAGGGACCCGGGAT[-/T]CCCATCCTCAGGGGT | 138151 |
| rs796544088 | in-del | -/AAGGAAAGGAAGG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136041095 | GAAGGAAGCAAAGGA[-/AAGGAAAGGAAGG]AAGGAAAGGAAGGAA | 138151 |
| rs796561896 | in-del | -/CA | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007520 | ACAGACGCGCACACA[-/CA]GACGCACAGACGTGC | 138151 |
| rs796563117 | multinucleotide-polymorphism | GTA/TTG | | | intron-variant | NACC2 | GRCh38.p7 | 9:136021556 | TGCTTGGTGGCTTCT[GTA/TTG]CAAGTTCAACATACA | 138151 |
| rs796588393 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136020883 | TGGGGCTTGAGCAAC[C/T]GGCCATCCGCACCCA | 138151 |
| rs796591690 | multinucleotide-polymorphism | CGG/TGT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136077048 | GCCGGGTGTGGTGGC[CGG/TGT]CGCCTGTAGTCCCAG | 138151 |
| rs796596986 | in-del | -/TTTTTT | | | intron-variant, upstream-variant-2KB | NACC2, LOC105376322 | GRCh38.p7 | 9:136012653 | ATTTGCCTCACAAGG[-/TTTTTT]TTTTTTTTTTTTTTT | 138151 |
| rs796634787 | in-del | -/CA | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007514 | ACATGCACAGACGCG[-/CA]CACACAGACGCACAG | 138151 |
| rs796637523 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136045154 | GTTCAGACCGCCCCA[C/T]GGAAGTGGGTACCCA | 138151 |
| rs796672791 | in-del | -/CA | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007408 | AGAGACACGCACGTG[-/CA]CACAGACGCGCGTGC | 138151 |
| rs796716647 | snp | C/G | | | intron-variant | NACC2 | GRCh38.p7 | 9:136081462 | CTGCTCTCTGAGCGC[C/G]GGGTGCCCAGGAAGG | 138151 |
| rs796759177 | in-del | AC/GCACAGACGT | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007525 | GCGCACACACAGACG[AC/GCACAGACGT]CACACACAGACACGC | 138151 |
| rs796775504 | in-del | -/A | | | intron-variant | NACC2 | GRCh38.p7 | 9:136093795 | GGTGGCCGGGAGAAG[-/A]AAGGGGTGGGTGGCT | 138151 |
| rs796784310 | in-del | CAGACGCACAGACGTG/GACGTGCA | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007520 | CAGACGCGCACACAC[CAGACGCACAGACGTG/GACGTGCA]ACACACAGACACGCA | 138151 |
| rs796866362 | multinucleotide-polymorphism | ATCGC/GTTGT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136074405 | TGCAGTGAGCCGAGG[ATCGC/GTTGT]CCACTGCACTCCAGC | 138151 |
| rs796868874 | snp | C/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136061841 | CGAAAAGTTGGTGGC[C/T]GGGCGCGGTGGCTCA | 138151 |
| rs796874843 | in-del | GACAGTGTGTGTGA/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136024534 | TGTGTGTGTGTGTGG[GACAGTGTGTGTGA/T]GACAGTGTGTGTAAG | 138151 |
| rs796904623 | in-del | -/CA | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136007474 | ACAGACGCACACACA[-/CA]GACGCACACACGCAC | 138151 |
| rs796948754 | snp | A/C | | | intron-variant | NACC2 | GRCh38.p7 | 9:136080800 | CACTGCAGAGGATGC[A/C]GGGAGAGCAGACGGC | 138151 |
| rs796956588 | in-del | -/T | | | intron-variant | NACC2 | GRCh38.p7 | 9:136090872 | TCTGCAGCATGGCTT[-/T]GCCGTTCACCCCAGT | 138151 |
| rs796975929 | in-del | -/TTTT | | | intron-variant | NACC2 | GRCh38.p7 | 9:136079059 | AATCATAGCTTCTTC[-/TTTT]TTTTTTTTTTAAGTG | 138151 |
| rs796986255 | snp | C/T | | | utr-variant-3-prime | NACC2 | GRCh38.p7 | 9:136008961 | GACGGCGATTACAAA[C/T]GAGTGAGGAAGGGGC | 138151 |