| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs570463355 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49573054 | TCATAACACCTCAAA[C/T]GGTCGAATATCACAA | 51070 |
| rs570493988 | snp | A/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49569839 | CAACAACAACAACAA[A/C]AAAGAACACTTGCAG | 51070 |
| rs570542313 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575991 | AAAAACAAAATTAGC[C/G]GGGCGTGGTGGCGGG | 51070 |
| rs570626339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49576744 | ACAAAATTAGCTGGG[C/T]GTGGTGGTGCATACC | 51070 |
| rs570689699 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49569292 | TCCACCTCCCAGGTT[C/T]ACACCATTCTCCTGC | 51070 |
| rs571032834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49567455 | AATTTACTAGTTGCT[C/T]TCCATACAGACTGCA | 51070 |
| rs571056551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49560095 | ACAGGAGACATGTCC[A/G]TCTCCAAAGCCCCAG | 51070 |
| rs571146662 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49581477 | GTGCTCACATTTCTG[A/G]GCAGGTAAGTGAATG | 51070 |
| rs571156348 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | NOSIP | GRCh38.p7 | 19:49574647 | CTACCAGCATTGTGG[A/G]GTTCTGGTGACACCC | 51070 |
| rs571209711 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NOSIP | GRCh38.p7 | 19:49573979 | ATTCTCCTGCCTCAG[A/C]CTCCCAAGTAGCTGG | 51070 |
| rs571264174 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NOSIP | GRCh38.p7 | 19:49566311 | AGGCGTGAGCCACTG[A/C]GCCCGGCCTTTTCTT | 51070 |
| rs571306778 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565602 | AAAAAATATATATAT[A/T]TAAAAATTTGCTGGG | 51070 |
| rs571501440 | in-del | -/A | 0.0115144 | 0.0749975 | intron-variant | NOSIP | GRCh38.p7 | 19:49561884 | GGCTCTGTCACAATT[-/A]AAAAAAAAAAAAAAA | 51070 |
| rs571545810 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580756 | TGGTGGGAATATGGG[G/T]AACGCTTACTATGTA | 51070 |
| rs571602809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49559133 | GCTGTTATACTCATG[A/G]TGATAGTTTACTGCA | 51070 |
| rs571629871 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49558351 | CCTCATGGGTTCAAG[A/C]GATTCTCCTGCCTCA | 51070 |
| rs571801371 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NOSIP, PRRG2 | GRCh38.p7 | 19:49579145 | AATTACTTAACTATA[C/T]CCTGATTCCAACAAA | 51070 |
| rs571833455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49570685 | ACCCCCAAGCTTCTC[A/G]GTGAACGTCCAACAC | 51070 |
| rs571897289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577294 | CGGGGCGCGGTGGCT[C/T]ATGCCTGTAATCCCA | 51070 |
| rs571942861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49568280 | GGTGTGGGGTGGAGG[A/G]AGCGCCTTGTGAATT | 51070 |
| rs571979680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565730 | GCCACTGCTCTCCAG[C/T]CTGGGCAATAGAGTG | 51070 |
| rs572137247 | in-del | -/AAAAG | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577553 | TCAAAAAAAGAAAAA[-/AAAAG]AAAAGAAGTATATCT | 51070 |
| rs572182396 | snp | C/T | 6.99729e-05 | 0.00591452 | utr-variant-3-prime | NOSIP | GRCh38.p7 | 19:49555714 | GGCGCCACGTCGTTG[C/T]GCACCCAAGCCGGTT | 51070 |
| rs572318868 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49574894 | TTGAGACGGAGTTTC[A/G]CTCTGTCACCCAGGC | 51070 |
| rs572390762 | snp | A/G | | | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49581486 | TTTCTGGGCAGGTAA[A/G]TGAATGTCCCTGGAG | 51070 |
| rs572426945 | in-del | -/A | | | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49578937 | TATTTTTAAATACTT[-/A]AAAAAAAAAAAGAAA | 51070 |
| rs572626381 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564529 | CCACAAGGGTTGCAA[C/T]TAGACAGAGGGGTGC | 51070 |
| rs572660925 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49574969 | CAGGGTTCATGCCAT[C/T]CTCCTGCCTCAGCCT | 51070 |
| rs572692006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575788 | GAATCACATATAATT[A/G]TCATAGGTCACCAAA | 51070 |
| rs572723644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49567185 | TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG | 51070 |
| rs572801549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49568187 | GTTTCACACGGGCTA[A/G]GTGGTTAAGACATAC | 51070 |
| rs572824018 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576330 | AAACCCTGTCTCTAC[C/G]AAAAAAAAGCAGCAG | 51070 |
| rs573047945 | snp | A/G | | | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49581685 | TGGGTGGATGTGACA[A/G]TGAGCACAGAAAGAG | 51070 |
| rs573050232 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NOSIP | GRCh38.p7 | 19:49574174 | GTCTTGCTCATTTAA[G/T]AGGTAGGAAAATTGA | 51070 |
| rs573164464 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580294 | GAGTTTATAGTGAGA[A/G]AGAGAGACAAAGAGA | 51070 |
| rs573241652 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580926 | CTGCATCTTAAAACA[A/G]TTGAGAAGAGACAAC | 51070 |
| rs573361643 | in-del | -/AT | | | intron-variant | NOSIP | GRCh38.p7 | 19:49571367 | ACCAAGGGTGGAAGA[-/AT]AGCCAGTTTCAGGAT | 51070 |
| rs573604465 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565249 | CTGCACTCCAGCCTG[C/G]GAGTCAGAGTGAGAC | 51070 |
| rs573853118 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577929 | TAGCAGAGTAGTGGC[A/T]GCCAAAGACTGGGGT | 51070 |
| rs573968290 | snp | C/G/T | 0.000115033 | 0.00758327 | intron-variant | NOSIP | GRCh38.p7 | 19:49557022 | AAGGGACTCAGATGC[C/G/T]GCCCCCTGGGCCCGC | 51070 |
| rs574031031 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49571545 | TCAGCATAATCCCTA[A/C]CTCACAGCACAGGAA | 51070 |
| rs574062883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49556460 | GGGAGACTCTGATCA[A/G]GGGCCTTCCTGGGGA | 51070 |
| rs574100228 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NOSIP | GRCh38.p7 | 19:49568221 | CATACTCCAAAAATA[C/T]GGCAGTTGACCTTGA | 51070 |
| rs574100813 | snp | A/G | | | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555322 | GAAGTGCAATGGTGC[A/G]ATCTTGGCTCACTGC | 51070 |
| rs574110097 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49569765 | GTGAGCCAAGATCGC[A/C/G]CCATCGCACTCCAGC | 51070 |
| rs574173368 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49563234 | AGGCTGGAGTGCAGT[A/G]GTACAATCACAGCTC | 51070 |
| rs574238591 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577155 | AACCCTTATACATTG[C/G]TGGTAGAAATGTAAA | 51070 |
| rs574288559 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49559209 | GGCAGAATCTAGTAG[A/G]GACTAGATTTGAGCT | 51070 |
| rs574308825 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49563820 | TGCTTTAGTGATCAC[C/G]CTGTTATATGTCTCT | 51070 |
| rs574309722 | snp | G/T | 0.00358779 | 0.0422022 | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555380 | TCTCCTGCCTCAGCC[G/T]CTGGAGTAGCTGGGA | 51070 |
| rs574528441 | snp | A/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49569178 | TGTAGGCACAGGAAA[A/T]CTACTGTGCATACAA | 51070 |
| rs574659560 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49570348 | ACTTGAAACACAAAC[C/T]TCTGGGAGCTATGGA | 51070 |
| rs574695892 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49578800 | TACAGGTGCCTGCCA[C/T]CATGCCCGGCTAAGG | 51070 |
| rs575054262 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580822 | TGGTTCCCAGGTTTT[G/T]AGTCTCTCCAAGCCC | 51070 |
| rs575168114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49582013 | GGGAGGCCGAGGCGG[A/G]TGGATCACTTGAGGT | 51070 |
| rs575258001 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575032 | CATGCCCGGCTAATT[A/T]TTTTGTATTTTTAGT | 51070 |
| rs575293406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49559436 | GGCAGGAGGATCACC[C/T]GAGCCTGGGATATCA | 51070 |
| rs575368724 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOSIP | GRCh38.p7 | 19:49574051 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 51070 |
| rs576303833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578122 | AGGTAAATCATATCC[C/T]ACTAATGCTTTTTTT | 51070 |
| rs576496446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49563032 | TGGAATCTAAATACT[A/G]TAATAATTTGAGACC | 51070 |
| rs576508124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49563766 | TCCCAAAGTGCTGGG[A/G]TTACAGGTGTGAGCC | 51070 |
| rs576513404 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576450 | GGCATAGTGGCATGC[A/G]CCTGTGGTCCCAGCT | 51070 |
| rs576563990 | snp | A/G | 3.59667e-05 | 0.00424052 | intron-variant | NOSIP | GRCh38.p7 | 19:49556302 | CTGGGGGAAGGGGAG[A/G]GGTGGGACTCTTACC | 51070 |
| rs576595393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577085 | TCACACCCCCTAGAA[C/T]GACTATAATCAAAAA | 51070 |
| rs576618425 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49567943 | TTGGCTTCTCAAAGT[C/G]CTGGGATTACAGGCA | 51070 |
| rs576651178 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49560514 | CCATCAGTGTATATC[A/G]GGGGCGGGAGAGAGA | 51070 |
| rs576701508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49569686 | GGTGGCAGGCGCCTG[C/T]AATCTCAGCTACTCA | 51070 |
| rs576709958 | snp | C/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49568838 | AGACAGAGTCTTGCT[C/G]TGTCACCAGGCTGGA | 51070 |
| rs576747374 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49567106 | TAGGCATGAGCCACC[A/G]TGCCCAGCCAAAAAA | 51070 |
| rs576770634 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555315 | CCAGGCTGAAGTGCA[A/G]TGGTGCGATCTTGGC | 51070 |
| rs576921957 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NOSIP | GRCh38.p7 | 19:49566383 | GTACAATCATAGCTC[A/G]CTGCAGCCTCAAACT | 51070 |
| rs576953499 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49567289 | CACCACACCGTATAA[C/T]TTTTTGTATTTTTAG | 51070 |
| rs577090472 | in-del | -/T | 0.185155 | 0.241444 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49566027 | TTTCTTTTCTTCTTC[-/T]TTTTTTTTTTTTGAG | 51070 |
| rs577117968 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49581994 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG | 51070 |
| rs577122963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49574193 | TAGGAAAATTGAAGC[C/T]TGGAGAAATTGGCCT | 51070 |
| rs577250530 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49578623 | CCAGCCTGGGCAACA[C/T]AGTGACACCTTGTCT | 51070 |
| rs577286186 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575055 | TTTTTAGTAGAGAGG[A/G]GGTTTCACCACGTTA | 51070 |
| rs577294932 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575566 | GGAAATTTAATCAAG[A/T]CTTTACATTCAATTT | 51070 |
| rs577510515 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49581100 | CTAGAGACCTAGATA[C/T]TAATTTTTCTAGCTC | 51070 |
| rs577516162 | in-del | -/TTTAT/TTTATTTTATTTTATG/TTTATTTTATTTTATTT | 0.0284343 | 0.116392 | intron-variant | NOSIP | GRCh38.p7 | 19:49573778 | CCCACGTTCTGCCCA[lengthTooLong]TTTATTTTATTTTAT | 51070 |
| rs577701495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565871 | GGTCTTTATGTGGCT[A/G]CAGATTCATCCCTGA | 51070 |
| rs577737426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49558767 | GAGAAGGATTTGGCC[A/G]GAAGCAGGGGAGGGG | 51070 |
| rs577774739 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580049 | AGGGGCTGTCAAAAA[A/G]GTGAAGAGAAGGTGG | 51070 |
| rs577927145 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NOSIP | GRCh38.p7 | 19:49572267 | CCCGCCACCATGCCT[A/G]GCTAATTTTTTGTAT | 51070 |
| rs577945426 | in-del | -/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579727 | TGTTGCAATTTTGTC[-/T]TTTGACAATCCTTAA | 51070 |
| rs578126932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49556493 | TACTGGCCCCAAAGC[C/T]GGACCGCCCCGCAGG | 51070 |
| rs578168985 | snp | C/G | 2.48889e-05 | 0.00352758 | intron-variant, missense | NOSIP | GRCh38.p7 | 19:49557085 | AGAAGCCCAACCTGA[C/G]TCACCTGGGCTGGTG | 51070 |
| rs578236776 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49563003 | AATTTCCAGCAACGT[A/G]AATGTGTAGCTGATG | 51070 |
| rs745440688 | snp | A/C | 0.00103805 | 0.0227584 | intron-variant | NOSIP | GRCh38.p7 | 19:49557033 | ATGCCGCCCCCTGGG[A/C]CCGCCCAGCCCGCGG | 51070 |
| rs745449754 | snp | C/T | | | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49581885 | TGCACACTGTGTGAC[C/T]TTCGGCAAGCTATAT | 51070 |
| rs745590059 | snp | A/G | 4.96849e-05 | 0.00498397 | intron-variant | NOSIP | GRCh38.p7 | 19:49559004 | AGGGTGCAATGAGAA[A/G]GAAAGAAAGTGATCC | 51070 |
| rs745595685 | in-del | -/AAAG | | | intron-variant | NOSIP | GRCh38.p7 | 19:49570111 | CTCATCTCAAAAAAT[-/AAAG]AAAGAATAAAATATA | 51070 |
| rs745601268 | snp | C/G | 1.76204e-05 | 0.00296814 | intron-variant | NOSIP | GRCh38.p7 | 19:49555862 | AGGTAGAGGCCGGCC[C/G]GGGGGTGACCAGTGG | 51070 |
| rs745611921 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49573493 | CAGCCTGGGTCCCAG[C/T]ATTGCCTGGCACCTG | 51070 |
| rs745664817 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575261 | GCCTTGGCCTCCCAC[A/G]GTGCTGGGATTATAG | 51070 |
| rs745689341 | in-del | -/TCTT | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579773 | CGATTTGTTTTAATC[-/TCTT]TAAGTTTAAAAAAAT | 51070 |
| rs745726047 | snp | C/T | 2.68539e-05 | 0.00366418 | intron-variant | NOSIP | GRCh38.p7 | 19:49556311 | GGGGAGGGGTGGGAC[C/T]CTTACCCGCTGCAGC | 51070 |
| rs745886518 | snp | A/G | 1.71655e-05 | 0.00292958 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49556578 | AGCGCAGGGGGTGGC[A/G]TTGCTCAGGCTGTCG | 51070 |
| rs746184028 | snp | A/T | | | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555125 | TGGCAAAAATCCGGG[A/T]ACCCTAACAAAGAAC | 51070 |
| rs746284308 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49578747 | TGCCTCCCGGGTTCA[C/T]GCAATTCTCCTGCCT | 51070 |
| rs746303854 | snp | A/G | 5.74399e-05 | 0.00535879 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49559948 | CGTGACAACAGGATC[A/G]TGGCAAGGCTGCAGG | 51070 |
| rs746353105 | snp | A/G | 1.70595e-05 | 0.00292052 | intron-variant | NOSIP | GRCh38.p7 | 19:49556506 | GCCGGACCGCCCCGC[A/G]GGTTCCCGAGTGGTC | 51070 |
| rs746455698 | snp | C/T | 1.64784e-05 | 0.00287035 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49557103 | ACCTGGGCTGGTGCC[C/T]GAGAGGGCCTTGGCT | 51070 |
| rs746528767 | snp | A/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49569887 | ATGCCTGAGGTGAGC[A/C]GATCACCTGAGGTCA | 51070 |
| rs746554130 | snp | C/T | | | intron-variant, utr-variant-5-prime | NOSIP | GRCh38.p7 | 19:49564162 | AAACGCACATTAAAA[C/T]TTCACTGAAGGCCGA | 51070 |
| rs746590664 | snp | A/G | 1.93571e-05 | 0.00311098 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555692 | GGGCGCCCACGCCGC[A/G]AATGAAGGCGCCACG | 51070 |
| rs746623559 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49570627 | CCCCAACTTGACCCA[A/G]GGTCCCCTCCACATG | 51070 |
| rs746645712 | snp | C/G | 1.66821e-05 | 0.00288804 | missense | NOSIP | GRCh38.p7 | 19:49555770 | GCCTGCATCACCGGC[C/G]GTGATTTCTCCGCTT | 51070 |
| rs746708642 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49561137 | GGACCAGCCCAGTGA[C/T]TGGCTCAAGGCTGGG | 51070 |
| rs746709394 | in-del | -/AGCTGGGC | 1.87623e-05 | 0.00306281 | frameshift-variant | NOSIP | GRCh38.p7 | 19:49556928 | GCGACGGGATCCAGA[-/AGCTGGGC]AGCACTTTGTCCTTG | 51070 |
| rs746815258 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49560789 | ATCTGCCCCCCTTGA[C/T]GGGAAAGCGGAGGCG | 51070 |
| rs746940610 | snp | C/T | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579943 | CCAAGTTCACAGAAT[C/T]AGCAGCACAATCAGA | 51070 |
| rs746981590 | snp | A/C | | | missense | NOSIP | GRCh38.p7 | 19:49556878 | GTGGGGGCTCACCGG[A/C]TTCTCCAGCTTGGTG | 51070 |
| rs747207194 | snp | A/C | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575482 | ATTTCACTACCCCTG[A/C]AAATGGGGCACCCAG | 51070 |
| rs747287256 | snp | C/T | 3.29924e-05 | 0.00406142 | intron-variant | NOSIP | GRCh38.p7 | 19:49558858 | CTCAGACTCAAAAGC[C/T]CCTGCCTCCGTGTGC | 51070 |
| rs747310901 | snp | A/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49560090 | GAGCAACAGGAGACA[A/T]GTCCGTCTCCAAAGC | 51070 |
| rs747435533 | snp | C/G | 5.49043e-05 | 0.00523919 | intron-variant | NOSIP | GRCh38.p7 | 19:49560708 | CTAGGGAGGAAGGGA[C/G]AGTGGCAGGACTGTG | 51070 |
| rs747441040 | snp | C/G | 3.8096e-05 | 0.00436423 | missense | NOSIP | GRCh38.p7 | 19:49556690 | ACGGGCGTCAGGTCC[C/G]ACATGCGCAGGGGCT | 51070 |
| rs747444141 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | PRRG2, NOSIP | GRCh38.p7 | 19:49580586 | AAGGAGCACTATTTT[C/T]CCCCTCCGCTCCGCC | 51070 |
| rs747462873 | snp | C/G/T | 6.89352e-05 | 0.00587058 | missense | NOSIP | GRCh38.p7 | 19:49556592 | CGTTGCTCAGGCTGT[C/G/T]GCGGGTCACGGCACA | 51070 |
| rs747614779 | snp | A/G | 3.3994e-05 | 0.0041226 | intron-variant | NOSIP | GRCh38.p7 | 19:49555838 | CTGGGGGAGGTAGAG[A/G]GAAGGACGAGGTAGA | 51070 |
| rs747640817 | snp | C/T | 1.67265e-05 | 0.00289188 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49555790 | TTTCTCCGCTTGCAG[C/T]TTCACTCCGGAGCCC | 51070 |
| rs747743679 | snp | C/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49557305 | TGGGGGTATCTTCCT[C/G]CCATTTCACAGGTAG | 51070 |
| rs747784159 | snp | C/T | 6.21949e-05 | 0.00557616 | intron-variant | NOSIP | GRCh38.p7 | 19:49560719 | GGGACAGTGGCAGGA[C/T]TGTGGTTACCGGAGG | 51070 |
| rs747871503 | in-del | -/TTTTTT | | | intron-variant | NOSIP | GRCh38.p7 | 19:49558248 | CACGTAGCACATCTT[-/TTTTTT]TTTTTTTTTTTTTGA | 51070 |
| rs747936839 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49562652 | TTGGGAAGCCGAGGC[A/G]GGGGCGGATCACGAG | 51070 |
| rs747954571 | snp | A/G | 4.06727e-05 | 0.0045094 | missense | NOSIP | GRCh38.p7 | 19:49557119 | GAGAGGGCCTTGGCT[A/G]TGAAAGGGTTGAGGG | 51070 |
| rs748001133 | snp | C/G | 1.86093e-05 | 0.0030503 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555699 | CACGCCGCGAATGAA[C/G]GCGCCACGTCGTTGC | 51070 |
| rs748092110 | snp | C/T | 2.41327e-05 | 0.00347358 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49557172 | CTTCTCCAGGAAGCC[C/T]CGCACATGGTCCTGC | 51070 |
| rs748168484 | in-del | -/TC | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577995 | ATGAGTACCAGGGTT[-/TC]TTTTTGGGTGATGAA | 51070 |
| rs748244489 | snp | A/G | | | intron-variant, utr-variant-5-prime | NOSIP | GRCh38.p7 | 19:49576777 | TAATCCCAGCTACTC[A/G]GGAGGCTGAAATGGG | 51070 |
| rs748280866 | snp | A/G | 1.65726e-05 | 0.00287855 | intron-variant | NOSIP | GRCh38.p7 | 19:49559012 | ATGAGAAAGAAAGAA[A/G]GTGATCCTCCCGCCT | 51070 |
| rs748368742 | in-del | -/AAC | | | intron-variant | NOSIP | GRCh38.p7 | 19:49569819 | GTCTCAAAAAACAAA[-/AAC]AACAACAACAACAAC | 51070 |
| rs748374339 | snp | C/T | 1.88649e-05 | 0.00307117 | missense | NOSIP | GRCh38.p7 | 19:49556331 | CCCGCTGCAGCACGA[C/T]GATGTCGCGGTCTGT | 51070 |
| rs748380393 | snp | G/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578031 | TTCTTAAAATGATAG[G/T]GTTGATGGTTGCACA | 51070 |
| rs748461813 | snp | A/G | 1.99209e-05 | 0.00315596 | missense | NOSIP | GRCh38.p7 | 19:49556717 | GGCTTCCCTGACATG[A/G]GGCAGGTCACCGTGC | 51070 |
| rs748769108 | snp | A/G | 6.76636e-05 | 0.00581612 | intron-variant | NOSIP | GRCh38.p7 | 19:49560730 | AGGACTGTGGTTACC[A/G]GAGGCAGGCAGCACA | 51070 |
| rs748863883 | snp | C/T | 1.84944e-05 | 0.00304086 | splice-donor-variant | NOSIP | GRCh38.p7 | 19:49556874 | CGCTGTGGGGGCTCA[C/T]CGGCTTCTCCAGCTT | 51070 |
| rs749163653 | snp | G/T | 6.43521e-05 | 0.00567203 | intron-variant | NOSIP | GRCh38.p7 | 19:49557265 | CTGCGTCGGGGAAAG[G/T]GGGCTGAGCATCTGC | 51070 |
| rs749174097 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49571390 | TTTCAGGATTTACAA[A/G]CTCTGAAAGCTGAGC | 51070 |
| rs749256234 | in-del | -/TT | | | intron-variant | NOSIP | GRCh38.p7 | 19:49561970 | TTTGATCATTTTAAC[-/TT]TTACTTTTTGAGTTA | 51070 |
| rs749330884 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578274 | GATTATAGGTGCCAG[C/T]CACCATGACCAGCCA | 51070 |
| rs749382696 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49562774 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAAACAGG | 51070 |
| rs749491556 | snp | C/G | 1.71493e-05 | 0.0029282 | missense | NOSIP | GRCh38.p7 | 19:49556570 | CGCAGCACAGCGCAG[C/G]GGGTGGCGTTGCTCA | 51070 |
| rs749617125 | snp | G/T | 2.53431e-05 | 0.00355962 | intron-variant | NOSIP | GRCh38.p7 | 19:49557002 | ACATCATCTGTGGGG[G/T]AAGGAAGGGACTCAG | 51070 |
| rs749742910 | in-del | -/AGAG | 4.40854e-05 | 0.00469476 | intron-variant | NOSIP | GRCh38.p7 | 19:49556748 | GGGACTGCAAGGGGC[-/AGAG]AGAGGCGGGCTCAGT | 51070 |
| rs749747891 | in-del | -/AAGGCAGGAAGATTGCTT | | | intron-variant | NOSIP | GRCh38.p7 | 19:49568711 | ACACTTTGGGAAACC[-/AAGGCAGGAAGATTGCTT]AAGGCCAGGAGTTCA | 51070 |
| rs749782359 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577071 | TAAAAGACACCAGTT[C/T]ACACCCCCTAGAATG | 51070 |
| rs749829794 | snp | C/G | 1.65891e-05 | 0.00287998 | intron-variant | NOSIP | GRCh38.p7 | 19:49559019 | AGAAAGAAAGTGATC[C/G]TCCCGCCTCGGCCTC | 51070 |
| rs749909012 | snp | C/T | 6.8417e-05 | 0.0058484 | intron-variant | NOSIP | GRCh38.p7 | 19:49556535 | TCCCTTCCCTCCCCT[C/T]CCAGGTGACTCACGA | 51070 |
| rs749947844 | in-del | -/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49572654 | CCATCAGATGCTAAA[-/T]TTTCATTGGAGATAC | 51070 |
| rs750047416 | in-del | -/TTT | | | intron-variant | NOSIP | GRCh38.p7 | 19:49568798 | AAAAAAAAAAAATAG[-/TTT]TTTGTTTGTTTGTTT | 51070 |
| rs750295905 | snp | A/C | 7.34754e-05 | 0.00606072 | intron-variant | NOSIP | GRCh38.p7 | 19:49559899 | GTTCCCTTGCTCTCC[A/C]CACCCAGACCTACCC | 51070 |
| rs750366685 | snp | C/G | 1.70084e-05 | 0.00291615 | missense | NOSIP | GRCh38.p7 | 19:49556415 | CGCATTCGAGGGTGA[C/G]CACAGCCCCACTACG | 51070 |
| rs750412036 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49560467 | CCACATGGGGTCATG[A/G]GATCACCCAGCTGTT | 51070 |
| rs750427177 | snp | C/G | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580494 | CCCAGCAACACTCTT[C/G]CTGCACCGCCTCGAA | 51070 |
| rs750493022 | in-del | -/CCCTC | 5.1343e-05 | 0.00506645 | intron-variant | NOSIP | GRCh38.p7 | 19:49556525 | CCCGAGTGGTCCCTT[-/CCCTC]CCCTCCCCTCCCAGG | 51070 |
| rs750523631 | snp | A/T | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49581383 | GCGCCCCTCCTCCTT[A/T]TCCCCTCCCCTCTTC | 51070 |
| rs750561273 | snp | C/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49562848 | TTGCACCACTACACT[C/G]CAGCCTGGTGACAGA | 51070 |
| rs750571557 | in-del | -/CCTCCCGCCTCGG | 1.65963e-05 | 0.0028806 | intron-variant | NOSIP | GRCh38.p7 | 19:49559018 | AAGAAAGAAAGTGAT[-/CCTCCCGCCTCGG]CCTCCCGAAGTGCTG | 51070 |
| rs750581523 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49559409 | GTGGTTCCAGCTACT[C/T]GTGGGGGCTGAGGCA | 51070 |
| rs750587774 | snp | C/T | 1.9078e-05 | 0.00308847 | intron-variant | NOSIP | GRCh38.p7 | 19:49556830 | GGACGGTGGGGAACC[C/T]TGGCGCCCTGGCACC | 51070 |
| rs750654408 | snp | G/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49568583 | TCAAAATAAGCATTA[G/T]AGCAGAACTGATGGT | 51070 |
| rs750671321 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49570434 | TATTTACACAGAATC[A/G]AAGCAAAGACCTTTA | 51070 |
| rs750758902 | snp | C/T | 6.67757e-05 | 0.00577784 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49555757 | CGCACACACTCAGGC[C/T]TGCATCACCGGCCGT | 51070 |
| rs750826206 | snp | C/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49558608 | AGGGTGGGAAAACTC[C/G]AAGTCCATAAGGGAA | 51070 |
| rs750845058 | in-del | -/CCT | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575297 | AGCCACCATGCGCAG[-/CCT]CCTCCTATTATAAGG | 51070 |
| rs750931959 | snp | A/G | 0.000118398 | 0.00769319 | intron-variant | NOSIP | GRCh38.p7 | 19:49555828 | CGGTACCGCCCTGGG[A/G]GAGGTAGAGAGAAGG | 51070 |
| rs751077357 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49567774 | CCTCCTGTGTTCAAG[C/T]GATTCTCCTGCCTCA | 51070 |
| rs751092563 | snp | C/G/T | 6.66161e-05 | 0.00577099 | missense | NOSIP | GRCh38.p7 | 19:49557158 | ACGATAGCCGACTCC[C/G/T]TCTCCAGGAAGCCCC | 51070 |
| rs751223804 | in-del | -/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49566526 | GGTTGGTCTTGAACT[-/C]CTGGGCTCAAGTGGT | 51070 |
| rs751309826 | snp | C/T | 0.000149699 | 0.00865027 | intron-variant | NOSIP | GRCh38.p7 | 19:49560065 | AGATGGGCAGAGTGA[C/T]GGAGGGGCGGAGCAA | 51070 |
| rs751319487 | snp | C/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577709 | GGTTGAGGCTGCAGT[C/G]AGCCATGATCGAACC | 51070 |
| rs751353745 | in-del | -/CTT | 1.64814e-05 | 0.00287061 | cds-indel | NOSIP | GRCh38.p7 | 19:49558918 | CTGCCGGGCAATCTC[-/CTT]CTTCTGGTGCAGAAT | 51070 |
| rs751378014 | snp | C/G | 1.71452e-05 | 0.00292785 | splice-donor-variant | NOSIP | GRCh38.p7 | 19:49556548 | CTCCCAGGTGACTCA[C/G]GAGGGCCGCAGCACA | 51070 |
| rs751441811 | snp | C/T | 5.20278e-05 | 0.00510012 | missense | NOSIP | GRCh38.p7 | 19:49556610 | GGGTCACGGCACACA[C/T]GTAGCGCTCGCTGCG | 51070 |
| rs751475250 | in-del | -/ATATATATATAC | | | intron-variant | NOSIP | GRCh38.p7 | 19:49566806 | TACATATATATATAT[-/ATATATATATAC]ACACACATACTATTT | 51070 |
| rs751487958 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49562403 | TGCTGGGATTACAGG[C/T]GTGAGTCACTGTGCC | 51070 |
| rs751556299 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49567721 | GTCGCCCAGGTTGGA[A/G]TGTAGTAGCATGATC | 51070 |
| rs751605503 | snp | C/T | 1.87852e-05 | 0.00306467 | intron-variant | NOSIP | GRCh38.p7 | 19:49556853 | CTGGCACCGTGCGTG[C/T]CGGGGCGCTGTGGGG | 51070 |
| rs751659630 | snp | C/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49559415 | CCAGCTACTCGTGGG[C/G]GCTGAGGCAGGAGGA | 51070 |
| rs751675122 | snp | A/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49568780 | CTAGACCCCATCTCT[A/T]AAAAAAAAAAAAAAA | 51070 |
| rs751690144 | snp | G/T | 2.31516e-05 | 0.00340225 | missense | NOSIP | GRCh38.p7 | 19:49556983 | CACACTGGGCCCAGG[G/T]TGGACATCATCTGTG | 51070 |
| rs751786349 | snp | G/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49556048 | GCCTTGGGAGGGAGC[G/T]TGTGGAGGGGGTGGA | 51070 |
| rs751845796 | in-del | -/G | 1.70705e-05 | 0.00292147 | intron-variant | NOSIP | GRCh38.p7 | 19:49556471 | ATCAGGGGCCTTCCT[-/G]GGGACCTACTGGCCC | 51070 |
| rs751917687 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578267 | TAGCTGGGATTATAG[A/G]TGCCAGCCACCATGA | 51070 |
| rs751972779 | snp | C/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49574344 | AGACTAAGTGTAAGA[C/G]AAATGGGAGAATAGG | 51070 |
| rs752043030 | snp | A/G | | | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49581511 | CTGGAGGAAGAGCCT[A/G]GCTTGGGGACCCAGG | 51070 |
| rs752257192 | snp | C/T | 1.64819e-05 | 0.00287066 | missense | NOSIP | GRCh38.p7 | 19:49558920 | GCCGGGCAATCTCCT[C/T]CTTCTGGTGCAGAAT | 51070 |
| rs752354604 | in-del | -/TTTTTTTT | | | intron-variant | NOSIP | GRCh38.p7 | 19:49558246 | TTCACGTAGCACATC[-/TTTTTTTT]TTTTTTTTTTTTTGA | 51070 |
| rs752379701 | snp | A/G | 5.39011e-05 | 0.00519111 | intron-variant | NOSIP | GRCh38.p7 | 19:49556291 | GCCTTGGAGTGCTGG[A/G]GGAAGGGGAGGGGTG | 51070 |
| rs752395532 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49579093 | GGAGTGGAAGGGGGA[A/G]CAGTTCTAAATTAAG | 51070 |
| rs752427783 | snp | C/T | | | synonymous-codon | NOSIP | GRCh38.p7 | 19:49558963 | GGCCTCACGCTCATA[C/T]AGGTAGCCATCTGGG | 51070 |
| rs752439711 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575771 | TTTTAGACTCTGACA[C/T]GGAATCACATATAAT | 51070 |
| rs752451382 | snp | G/T | 1.74732e-05 | 0.00295572 | missense | NOSIP | GRCh38.p7 | 19:49556627 | TAGCGCTCGCTGCGG[G/T]TGATGAGCCCCACGC | 51070 |
| rs752502677 | snp | A/G | 0.000251913 | 0.0112202 | intron-variant | NOSIP | GRCh38.p7 | 19:49556780 | GTAGGCAGGGCTGGC[A/G]CAGGTGGAGAGCGCG | 51070 |
| rs752530522 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49567424 | CCGTGCCCGGCCCCA[A/G]AAATTTTTTTGTTAG | 51070 |
| rs752580744 | in-del | -/T | 6.46559e-05 | 0.0056854 | intron-variant | NOSIP | GRCh38.p7 | 19:49556288 | GGGGCCTTGGAGTGC[-/T]GGGGGAAGGGGAGGG | 51070 |
| rs752675890 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565388 | GGGTGCTGGTTACAT[A/G]GGTGTGTTTGCTCTG | 51070 |
| rs752822524 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49570191 | ATTCAGGAAAGATTG[C/T]CTCCTGCTCTCAAGT | 51070 |
| rs752836348 | snp | A/C/T | 4.25044e-05 | 0.00460981 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555669 | CATCCTCGCCTGCCC[A/C/T]GTCCCCGGGGCGCCC | 51070 |
| rs753007400 | in-del | -/A | | | intron-variant | NOSIP | GRCh38.p7 | 19:49572973 | TCAAGACTGTGTCTC[-/A]AAAAAAAAAAAAAAA | 51070 |
| rs753088731 | snp | A/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49570093 | CAGCCTGGGTGACAG[A/T]CACTCATCTCAAAAA | 51070 |
| rs753236913 | snp | G/T | 2.40769e-05 | 0.00346957 | missense | NOSIP | GRCh38.p7 | 19:49556993 | CCAGGTTGGACATCA[G/T]CTGTGGGGGAAGGAA | 51070 |
| rs753242658 | snp | C/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49570409 | GAAGCCACTCTTTGG[C/G]TTTTAGGTATATTTA | 51070 |
| rs753349099 | snp | A/G | 1.66114e-05 | 0.00288192 | intron-variant | NOSIP | GRCh38.p7 | 19:49559029 | TGATCCTCCCGCCTC[A/G]GCCTCCCGAAGTGCT | 51070 |
| rs753350769 | snp | A/G | 3.49046e-05 | 0.00417745 | intron-variant | NOSIP | GRCh38.p7 | 19:49556303 | TGGGGGAAGGGGAGG[A/G]GTGGGACTCTTACCC | 51070 |
| rs753574120 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49561884 | GGCTCTGTCACAATT[A/G]AAAAAAAAAAAAAAA | 51070 |
| rs753806135 | snp | C/T | 1.65111e-05 | 0.0028732 | missense | NOSIP | GRCh38.p7 | 19:49558967 | TCACGCTCATACAGG[C/T]AGCCATCTGGGCTGC | 51070 |
| rs753970548 | snp | G/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NOSIP, PRRG2 | GRCh38.p7 | 19:49579249 | GTGTGATGATGGTAT[G/T]GTGGTCATATCAGCA | 51070 |
| rs754038546 | snp | C/T | 0.000139247 | 0.0083429 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49560662 | GGTGTAGACGGCCCC[C/T]GCGGTGCAGTTCTTG | 51070 |
| rs754099438 | snp | A/G | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580208 | CCCTTGGGACCACCA[A/G]CAAATAGCCATCATC | 51070 |
| rs754158524 | snp | A/C/G/T | 0.000365075 | 0.0135066 | intron-variant, splice-donor-variant | NOSIP | GRCh38.p7 | 19:49557079 | CCCACAAGAAGCCCA[A/C/G/T]CCTGAGTCACCTGGG | 51070 |
| rs754345292 | in-del | -/CTT | 0.000277277 | 0.0117712 | cds-indel | NOSIP | GRCh38.p7 | 19:49560629 | CCCTGCACCTGTGTC[-/CTT]CTTCTTCTCGTGGTA | 51070 |
| rs754347770 | snp | A/C/T | 4.26596e-05 | 0.00461826 | missense | NOSIP | GRCh38.p7 | 19:49557147 | GGGGCCGGCTCACGA[A/C/T]AGCCGACTCCTTCTC | 51070 |
| rs754491390 | snp | G/T | 4.63704e-05 | 0.00481488 | missense | NOSIP | GRCh38.p7 | 19:49557240 | GGGTGCCCCGCTGCT[G/T]CTCGTAGGCCTGCGT | 51070 |
| rs754527587 | snp | C/T | 1.66935e-05 | 0.00288903 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49555781 | CGGCCGTGATTTCTC[C/T]GCTTGCAGCTTCACT | 51070 |
| rs754728597 | snp | G/T | 1.71305e-05 | 0.00292659 | missense | NOSIP | GRCh38.p7 | 19:49556553 | AGGTGACTCACGAGG[G/T]CCGCAGCACAGCGCA | 51070 |
| rs754801252 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577888 | TCATTTGTGCAAAAT[A/G]CCCAGATTAGGCAAA | 51070 |
| rs754857064 | in-del | -/CTTTTT | | | intron-variant | NOSIP | GRCh38.p7 | 19:49558245 | ATTCACGTAGCACAT[-/CTTTTT]TTTTTTTTTTTTTTT | 51070 |
| rs754875154 | in-del | -/CA | | | intron-variant | NOSIP | GRCh38.p7 | 19:49560351 | TCCCTCTTTGGGCCT[-/CA]GTTTCTTCCTCTGGA | 51070 |
| rs754946456 | snp | C/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49569008 | GGCTTTCACCACGTT[C/G]GTCACGATGGTCTCG | 51070 |
| rs754987466 | in-del | -/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49568779 | GCTAGACCCCATCTC[-/T]AAAAAAAAAAAAAAA | 51070 |
| rs755108331 | snp | C/T | 2.36521e-05 | 0.00343882 | missense | NOSIP | GRCh38.p7 | 19:49556988 | TGGGCCCAGGTTGGA[C/T]ATCATCTGTGGGGGA | 51070 |
| rs755229511 | snp | C/G | 1.65627e-05 | 0.00287769 | intron-variant | NOSIP | GRCh38.p7 | 19:49559005 | GGGTGCAATGAGAAA[C/G]AAAGAAAGTGATCCT | 51070 |
| rs755343511 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49568424 | AAGTGCCGTGTATGT[A/G]TGCTTTGTGTATTCC | 51070 |
| rs755368002 | snp | A/G | 5.55942e-05 | 0.005272 | intron-variant | NOSIP | GRCh38.p7 | 19:49560710 | AGGGAGGAAGGGACA[A/G]TGGCAGGACTGTGGT | 51070 |
| rs755532915 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49567722 | TCGCCCAGGTTGGAG[C/T]GTAGTAGCATGATCT | 51070 |
| rs755552712 | snp | C/G | 1.87682e-05 | 0.00306329 | intron-variant | NOSIP | GRCh38.p7 | 19:49556855 | GGCACCGTGCGTGCC[C/G]GGGCGCTGTGGGGGC | 51070 |
| rs755682821 | snp | A/G | 1.64833e-05 | 0.00287078 | missense | NOSIP | GRCh38.p7 | 19:49558929 | TCTCCTTCTTCTGGT[A/G]CAGAATGTACTCCAG | 51070 |
| rs755707045 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49557306 | GGGGGTATCTTCCTC[C/T]CATTTCACAGGTAGG | 51070 |
| rs755919783 | snp | A/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565453 | CTTCTCTGTACATGT[A/T]ATAAAAAGAAATTGG | 51070 |
| rs756135878 | snp | A/C/G | 0.000240592 | 0.0109657 | intron-variant | NOSIP | GRCh38.p7 | 19:49557257 | TCGTAGGCCTGCGTC[A/C/G]GGGAAAGTGGGCTGA | 51070 |
| rs756236611 | in-del | -/GCAGAGTGATGGAGGGGCGGA | 3.29484e-05 | 0.00405871 | intron-variant | NOSIP | GRCh38.p7 | 19:49560055 | TGGGGACAGAGATGG[-/GCAGAGTGATGGAGGGGCGGA]GCAGAGTGATGGAGG | 51070 |
| rs756292820 | snp | C/T | 2.86981e-05 | 0.00378791 | intron-variant | NOSIP | GRCh38.p7 | 19:49559918 | CCAGACCTACCCATC[C/T]CTGTTCCCAGCTCAC | 51070 |
| rs756303741 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578076 | CTAAACACCACTGAA[C/T]TGTATATTTTCAATG | 51070 |
| rs756346141 | snp | A/G | 2.19551e-05 | 0.00331317 | intron-variant | NOSIP | GRCh38.p7 | 19:49560069 | GGGCAGAGTGATGGA[A/G]GGGCGGAGCAACAGG | 51070 |
| rs756382131 | in-del | -/AAG | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577560 | AAGAAAAAAAAAGAA[-/AAG]AAGTATATCTTGGGT | 51070 |
| rs756603189 | snp | A/C | 1.64939e-05 | 0.0028717 | intron-variant | NOSIP | GRCh38.p7 | 19:49557072 | CCCCCAACCCACAAG[A/C]AGCCCAACCTGAGTC | 51070 |
| rs756619279 | in-del | -/AG | 3.42255e-05 | 0.00413661 | intron-variant | NOSIP | GRCh38.p7 | 19:49556538 | CTTCCCTCCCCTCCC[-/AG]GTGACTCACGAGGGC | 51070 |
| rs756689789 | in-del | -/TCCTGTG | | | intron-variant | NOSIP | GRCh38.p7 | 19:49567761 | TGCAACCTCTCTGCC[-/TCCTGTG]TTCAAGCGATTCTCC | 51070 |
| rs756719408 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575967 | AAACCCCGTCTCTAC[C/T]AATAATACAAAAACA | 51070 |
| rs756824747 | snp | A/T | 1.69864e-05 | 0.00291426 | missense | NOSIP | GRCh38.p7 | 19:49556404 | CAGCTTCTCCACGCA[A/T]TCGAGGGTGACCACA | 51070 |
| rs756846939 | snp | G/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49560138 | AGACAACGCGGTGGT[G/T]GGGGTGGGGGACTCA | 51070 |
| rs757162441 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575155 | GGCGTGAGCCACTGC[A/G]CCCGGCCTCATTTTT | 51070 |
| rs757220647 | snp | A/G | 3.3077e-05 | 0.00406662 | intron-variant | NOSIP | GRCh38.p7 | 19:49558989 | CTGGGCTGCAAAGAC[A/G]GGGTGCAATGAGAAA | 51070 |
| rs757270984 | snp | A/G | 2.37437e-05 | 0.00344547 | intron-variant | NOSIP | GRCh38.p7 | 19:49560074 | GAGTGATGGAGGGGC[A/G]GAGCAACAGGAGACA | 51070 |
| rs757271965 | snp | A/G | 7.77756e-05 | 0.00623552 | intron-variant | NOSIP | GRCh38.p7 | 19:49559883 | CAGCCTCCTCCTGGC[A/G]GTTCCCTTGCTCTCC | 51070 |
| rs757274147 | snp | A/C/G | 6.7607e-05 | 0.00581376 | intron-variant | NOSIP | GRCh38.p7 | 19:49556304 | GGGGGAAGGGGAGGG[A/C/G]TGGGACTCTTACCCG | 51070 |
| rs757369043 | snp | C/G | 1.71578e-05 | 0.00292893 | missense | NOSIP | GRCh38.p7 | 19:49556571 | GCAGCACAGCGCAGG[C/G]GGTGGCGTTGCTCAG | 51070 |
| rs757408096 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NOSIP, PRRG2 | GRCh38.p7 | 19:49579252 | TGATGATGGTATTGT[A/G]GTCATATCAGCAATG | 51070 |
| rs757493593 | snp | A/G | 1.76107e-05 | 0.00296733 | missense | NOSIP | GRCh38.p7 | 19:49556634 | CGCTGCGGGTGATGA[A/G]CCCCACGCGGTCCAC | 51070 |
| rs757494584 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49570542 | TAAATACCCCCTCAC[A/G]CCCCTTCCCGATCAA | 51070 |
| rs757495143 | in-del | -/C | 3.41119e-05 | 0.00412975 | intron-variant | NOSIP | GRCh38.p7 | 19:49556499 | CCCAAAGCCGGACCG[-/C]CCCCGCAGGTTCCCG | 51070 |
| rs757635376 | snp | A/G | | | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555087 | GGAAGACACGTTCCT[A/G]GGCATTTCCTGTTCT | 51070 |
| rs757681576 | snp | A/C | 2.06031e-05 | 0.00320953 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555682 | CCTGTCCCCGGGGCG[A/C]CCACGCCGCGAATGA | 51070 |
| rs757747143 | snp | C/G | 3.70851e-05 | 0.00430595 | missense | NOSIP | GRCh38.p7 | 19:49556676 | GCGGTGTGAAGTGCA[C/G]GGGCGTCAGGTCCGA | 51070 |
| rs758003362 | snp | A/G | 2.43442e-05 | 0.00348877 | splice-donor-variant, synonymous-codon | NOSIP | GRCh38.p7 | 19:49557088 | AGCCCAACCTGAGTC[A/G]CCTGGGCTGGTGCCC | 51070 |
| rs758056354 | snp | G/T | 2.16537e-05 | 0.00329035 | stop-gained | NOSIP | GRCh38.p7 | 19:49557152 | CGGCTCACGATAGCC[G/T]ACTCCTTCTCCAGGA | 51070 |
| rs758084194 | in-del | -/GACAGC | | | intron-variant | NOSIP | GRCh38.p7 | 19:49558638 | AGTGGGCATGTGTCA[-/GACAGC]GACAGCCACATGTAC | 51070 |
| rs758088578 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49569782 | CATCGCACTCCAGCC[C/T]GGGGGACAAGAGTGA | 51070 |
| rs758112608 | snp | C/G | 3.31724e-05 | 0.00407248 | intron-variant | NOSIP | GRCh38.p7 | 19:49559909 | TCTCCCCACCCAGAC[C/G]TACCCATCCCTGTTC | 51070 |
| rs758171611 | snp | A/G | 1.70513e-05 | 0.00291982 | intron-variant | NOSIP | GRCh38.p7 | 19:49556430 | CCACAGCCCCACTAC[A/G]GTGAGGCCGAAGGCG | 51070 |
| rs758218064 | snp | A/G | | | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49582420 | GTTGGGATTACAGGC[A/G]CCCACAACCACGCCT | 51070 |
| rs758236080 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576433 | ATTTAAAAAATTAGC[C/T]GGGCATAGTGGCATG | 51070 |
| rs758337740 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49567591 | CTGCACCATGCTGTG[A/G]AAAATGTGCCATCAG | 51070 |
| rs758358551 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577489 | TCAAACCTGGGAGCC[A/G]AGATCACGCCACTGC | 51070 |
| rs758374592 | snp | A/G | 1.71187e-05 | 0.00292559 | intron-variant | NOSIP | GRCh38.p7 | 19:49556539 | TTCCCTCCCCTCCCA[A/G]GTGACTCACGAGGGC | 51070 |
| rs758504138 | snp | A/C | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565661 | TACTCAGGAGGCTGA[A/C]GCAGGAGGACTGCTT | 51070 |
| rs758542969 | snp | C/T | 3.78723e-05 | 0.00435141 | intron-variant | NOSIP | GRCh38.p7 | 19:49556844 | CCTGGCGCCCTGGCA[C/T]CGTGCGTGCCGGGGC | 51070 |
| rs758747462 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49573470 | TTGGTGGGGCCTGGG[C/T]TGAACTTCAGCCTGG | 51070 |
| rs758815992 | snp | G/T | 1.6922e-05 | 0.00290873 | intron-variant | NOSIP | GRCh38.p7 | 19:49555829 | GGTACCGCCCTGGGG[G/T]AGGTAGAGAGAAGGA | 51070 |
| rs758910788 | snp | A/G | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49581037 | ACTGCGGCACTGCCC[A/G]GCTGTCCCAGGGACT | 51070 |
| rs758963880 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime | PRRG2, NOSIP | GRCh38.p7 | 19:49580527 | CACCTCACTAACGAC[G/T]CCCAGTCCCTCGGTC | 51070 |
| rs758989822 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565179 | TACTTGGGAGTCTGA[A/G]ATGGATCACCTGAGC | 51070 |
| rs758989830 | snp | A/G | 1.83998e-05 | 0.00303308 | missense | NOSIP | GRCh38.p7 | 19:49556918 | TCGGGCGTCAGCGAC[A/G]GGATCCAGAAGCTGG | 51070 |
| rs759059897 | in-del | -/C | 0.000149014 | 0.00863045 | frameshift-variant | NOSIP | GRCh38.p7 | 19:49557143 | TGAGGGGCCGGCTCA[-/C]CGATAGCCGACTCCT | 51070 |
| rs759090020 | in-del | -/TCTTTTTT | | | intron-variant | NOSIP | GRCh38.p7 | 19:49558244 | AATTCACGTAGCACA[-/TCTTTTTT]TTTTTTTTTTTTTTT | 51070 |
| rs759230633 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555655 | TTTGCACGGCCCTGC[A/G]TCCTCGCCTGCCCTG | 51070 |
| rs759258487 | snp | G/T | | | missense | NOSIP | GRCh38.p7 | 19:49558914 | TCATCTGCCGGGCAA[G/T]CTCCTTCTTCTGGTG | 51070 |
| rs759325179 | snp | C/T | 4.65625e-05 | 0.00482484 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49560659 | GTAGGTGTAGACGGC[C/T]CCTGCGGTGCAGTTC | 51070 |
| rs759426411 | snp | C/G | 3.48384e-05 | 0.00417348 | missense | NOSIP | GRCh38.p7 | 19:49556619 | CACACACGTAGCGCT[C/G]GCTGCGGGTGATGAG | 51070 |
| rs759453364 | in-del | -/CA | 3.34902e-05 | 0.00409194 | utr-variant-3-prime | NOSIP | GRCh38.p7 | 19:49555744 | TTATTTGGTCTCCCG[-/CA]CACACTCAGGCCTGC | 51070 |
| rs759502889 | snp | G/T | 6.33714e-05 | 0.00562865 | intron-variant | NOSIP | GRCh38.p7 | 19:49556774 | GGCTCAGTAGGCAGG[G/T]CTGGCGCAGGTGGAG | 51070 |
| rs759670667 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49570365 | CTGGGAGCTATGGAG[C/T]TCTCTCTCCCCCTAC | 51070 |
| rs759704726 | snp | A/C | 2.13045e-05 | 0.00326371 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555667 | TGCATCCTCGCCTGC[A/C]CTGTCCCCGGGGCGC | 51070 |
| rs759723566 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49571676 | CAGTTTTCCTAGGAA[A/G]GTCACAATCTCAGAA | 51070 |
| rs759741798 | snp | A/C | 0.00022193 | 0.0105317 | intron-variant | NOSIP | GRCh38.p7 | 19:49557056 | GCCCGCGGCGCCCCG[A/C]CCCCCAACCCACAAG | 51070 |
| rs759763761 | snp | G/T | | | missense | NOSIP | GRCh38.p7 | 19:49558949 | ATGTACTCCAGGATG[G/T]CCTCACGCTCATACA | 51070 |
| rs759827174 | snp | A/G | 5.74828e-05 | 0.00536079 | intron-variant | NOSIP | GRCh38.p7 | 19:49556289 | GGGCCTTGGAGTGCT[A/G]GGGGAAGGGGAGGGG | 51070 |
| rs759871943 | snp | C/G | 2.08644e-05 | 0.00322983 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49557133 | TGTGAAAGGGTTGAG[C/G]GGCCGGCTCACGATA | 51070 |
| rs759887594 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577160 | TTATACATTGGTGGT[A/G]GAAATGTAAAATGGT | 51070 |
| rs759921161 | snp | C/T | 4.56506e-05 | 0.00477737 | intron-variant | NOSIP | GRCh38.p7 | 19:49560073 | AGAGTGATGGAGGGG[C/T]GGAGCAACAGGAGAC | 51070 |
| rs760052107 | snp | C/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49568327 | AAGAGGGTTATTTGA[C/G]ATCTGATGGAAAGTC | 51070 |
| rs760203365 | in-del | -/GA | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580291 | CTGAGTTTATAGTGA[-/GA]GAGAGAGAGACAAAG | 51070 |
| rs760275027 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575781 | TGACACGGAATCACA[C/T]ATAATTGTCATAGGT | 51070 |
| rs760309836 | in-del | -/AAA | | | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49582239 | AGCGAGACTCTGTCT[-/AAA]AAAAAAAAAAAAAAA | 51070 |
| rs760314903 | in-del | -/C | 2.13952e-05 | 0.00327065 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555666 | CTGCATCCTCGCCTG[-/C]CCTGTCCCCGGGGCG | 51070 |
| rs760406810 | snp | A/C/T | 0.000101938 | 0.00713859 | missense | NOSIP | GRCh38.p7 | 19:49556400 | GAATCAGCTTCTCCA[A/C/T]GCATTCGAGGGTGAC | 51070 |
| rs760425715 | snp | A/G | 3.50607e-05 | 0.00418678 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49559981 | GAGACAACAGCAGTC[A/G]AAGTCCTTCACGGCA | 51070 |
| rs760457647 | snp | A/G | 3.06556e-05 | 0.00391495 | intron-variant | NOSIP | GRCh38.p7 | 19:49556784 | GCAGGGCTGGCGCAG[A/G]TGGAGAGCGCGTGGT | 51070 |
| rs760478690 | snp | C/T | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579983 | CATGACTGCCTGACC[C/T]CGAAGCTCCACACAA | 51070 |
| rs760603713 | snp | C/T | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49581158 | AGAGCGGGTAGGGGT[C/T]GGGAGGGAGGAGGAG | 51070 |
| rs760627706 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49566539 | CTCCTGGGCTCAAGT[A/G]GTCCTCCTGCTTTGG | 51070 |
| rs760725593 | snp | A/G | 0.000218815 | 0.0104575 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49557202 | CGAGGCCGCCCGCTG[A/G]AGCTCCTTCTGCTCC | 51070 |
| rs760841677 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49557918 | GACCACCAGGCTGTG[C/T]GGAGGACATGGGCAC | 51070 |
| rs761009026 | snp | A/G | 1.68468e-05 | 0.00290226 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49555814 | GGAGCCCGCGAAGCC[A/G]GTACCGCCCTGGGGG | 51070 |
| rs761155161 | snp | C/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49556820 | TGCGTGAGGAGGACG[C/G]TGGGGAACCCTGGCG | 51070 |
| rs761430952 | snp | C/T | 0.000148434 | 0.00861365 | intron-variant | NOSIP | GRCh38.p7 | 19:49560596 | GACACAGCCATGTCC[C/T]GCCTCTTCCCACCCC | 51070 |
| rs761460943 | snp | C/T | 1.71021e-05 | 0.00292416 | intron-variant | NOSIP | GRCh38.p7 | 19:49556523 | GTTCCCGAGTGGTCC[C/T]TTCCCTCCCCTCCCA | 51070 |
| rs761570807 | in-del | -/CTT | | | intron-variant, cds-indel | NOSIP | GRCh38.p7 | 19:49574721 | GCTCTCTGGTGTCTC[-/CTT]CTGTTTTTTGGGAGG | 51070 |
| rs761598646 | snp | A/C | 1.66849e-05 | 0.00288828 | intron-variant | NOSIP | GRCh38.p7 | 19:49557046 | GGCCCGCCCAGCCCG[A/C]GGCGCCCCGCCCCCC | 51070 |
| rs761781172 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49558588 | TTACTAAGGACCTAA[A/G]CTACAGGGTGGGAAA | 51070 |
| rs761858743 | snp | A/G | 1.76974e-05 | 0.00297462 | intron-variant | NOSIP | GRCh38.p7 | 19:49555867 | GAGGCCGGCCCGGGG[A/G]TGACCAGTGGGGCTC | 51070 |
| rs761898984 | snp | G/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575648 | GAGAGTAAATGTTTT[G/T]AACTTTGCAGGCCAA | 51070 |
| rs761989429 | in-del | -/AGAA | 0.000165551 | 0.00909659 | intron-variant | NOSIP | GRCh38.p7 | 19:49559000 | AGACAGGGTGCAATG[-/AGAA]AGAAAGAAAGTGATC | 51070 |
| rs762021851 | snp | A/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49559620 | TGCCTGGACTCAGCA[A/C]CTGTTAAGCCTTTGC | 51070 |
| rs762155305 | snp | C/G | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49581296 | CCTTACCTGAGTCCC[C/G]CCCAGGGCAGGTAAT | 51070 |
| rs762261541 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49574274 | TGGAAGTTTGATTAA[A/G]TCACTCTCTTCAACT | 51070 |
| rs762403392 | snp | A/C | 3.46891e-05 | 0.00416453 | missense | NOSIP | GRCh38.p7 | 19:49557211 | CCGCTGAAGCTCCTT[A/C]TGCTCCTCGCGCCGG | 51070 |
| rs762510311 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49563771 | AAGTGCTGGGATTAC[A/G]GGTGTGAGCCACTGT | 51070 |
| rs762575134 | in-del | -/ATAT | | | intron-variant | NOSIP | GRCh38.p7 | 19:49572676 | TGGAGATACTTTAAA[-/ATAT]ATATATATATATGGC | 51070 |
| rs762823521 | snp | C/T | 1.65293e-05 | 0.00287479 | missense | NOSIP | GRCh38.p7 | 19:49560631 | CTGCACCTGTGTCCT[C/T]CTTCTTCTCGTGGTA | 51070 |
| rs762843467 | snp | A/G | 3.84445e-05 | 0.00438415 | missense | NOSIP | GRCh38.p7 | 19:49560039 | CCATAGCCCGAGGCC[A/G]CTGGGGACAGAGATG | 51070 |
| rs762872976 | in-del | -/G | 1.71277e-05 | 0.00292635 | intron-variant | NOSIP | GRCh38.p7 | 19:49556445 | GGTGAGGCCGAAGGC[-/G]GGAGACTCTGATCAG | 51070 |
| rs762928085 | in-del | -/CTGCC | 1.6908e-05 | 0.00290753 | intron-variant | NOSIP | GRCh38.p7 | 19:49557277 | AAGTGGGCTGAGCAT[-/CTGCC]CGTGGGGCTGGGGGT | 51070 |
| rs762934206 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555562 | CCGTGCCTGGCCAGA[G/T]TTTGTTCTTAATGTG | 51070 |
| rs762959254 | snp | A/G | 3.61083e-05 | 0.00424886 | missense | NOSIP | GRCh38.p7 | 19:49556340 | GCACGATGATGTCGC[A/G]GTCTGTGAGTTTGTC | 51070 |
| rs763103809 | snp | A/G | 4.19164e-05 | 0.00457782 | missense | NOSIP | GRCh38.p7 | 19:49556961 | CCTTGTCCTTACTTG[A/G]AGGACCCACACTGGG | 51070 |
| rs763223523 | in-del | -/C | | | frameshift-variant | NOSIP | GRCh38.p7 | 19:49557205 | GGCCGCCCGCTGAAG[-/C]TCCTTCTGCTCCTCG | 51070 |
| rs763270571 | snp | C/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49568600 | GCAGAACTGATGGTA[C/G]ATGAAACTCCAGCAA | 51070 |
| rs763344114 | snp | A/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49574471 | CACAGGATGCTAATT[A/C]TTGCTACTGGAAAAT | 51070 |
| rs763487028 | snp | A/G | 1.66524e-05 | 0.00288547 | intron-variant | NOSIP | GRCh38.p7 | 19:49556281 | GAGGGGCGGGGCCTT[A/G]GAGTGCTGGGGGAAG | 51070 |
| rs763577662 | in-del | -/AAAG | | | intron-variant | NOSIP | GRCh38.p7 | 19:49570114 | TCTCAAAAAATAAAG[-/AAAG]AAAGAATAAAATATA | 51070 |
| rs763728144 | snp | C/T | 0.000166088 | 0.00911134 | intron-variant | NOSIP | GRCh38.p7 | 19:49559028 | GTGATCCTCCCGCCT[C/T]GGCCTCCCGAAGTGC | 51070 |
| rs763763680 | snp | C/T | 2.06909e-05 | 0.00321637 | missense | NOSIP | GRCh38.p7 | 19:49556957 | TTGTCCTTGTCCTTA[C/T]TTGGAGGACCCACAC | 51070 |
| rs763832392 | in-del | -/AAGG | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565782 | AAAAAGAAAGAAAGA[-/AAGG]AAGAAATTAATGGCG | 51070 |
| rs763841499 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49560129 | GAGGCACAGAGACAA[C/T]GCGGTGGTGGGGGTG | 51070 |
| rs763895142 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49566583 | TAGGATGAAGGGTAT[A/G]AGCTACTGCACCCAA | 51070 |
| rs763906860 | snp | C/T | 1.70874e-05 | 0.00292291 | intron-variant | NOSIP | GRCh38.p7 | 19:49556520 | CAGGTTCCCGAGTGG[C/T]CCCTTCCCTCCCCTC | 51070 |
| rs763926501 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565459 | TGTACATGTTATAAA[A/G]AGAAATTGGCTGGGT | 51070 |
| rs763933444 | in-del | -/CT | 1.70854e-05 | 0.00292274 | intron-variant | NOSIP | GRCh38.p7 | 19:49556451 | GCCGAAGGCGGGAGA[-/CT]CTGATCAGGGGCCTT | 51070 |
| rs763988310 | in-del | -/CTC | 1.64815e-05 | 0.00287063 | cds-indel | NOSIP | GRCh38.p7 | 19:49558915 | CATCTGCCGGGCAAT[-/CTC]CTTCTTCTGGTGCAG | 51070 |
| rs764184868 | snp | A/G | 4.95013e-05 | 0.00497475 | missense | NOSIP | GRCh38.p7 | 19:49558956 | CCAGGATGGCCTCAC[A/G]CTCATACAGGTAGCC | 51070 |
| rs764246231 | snp | C/T | 1.69795e-05 | 0.00291367 | utr-variant-3-prime | NOSIP | GRCh38.p7 | 19:49555725 | GTTGCGCACCCAAGC[C/T]GGTTTATTTGGTCTC | 51070 |
| rs764358157 | snp | C/T | 4.63575e-05 | 0.00481421 | missense | NOSIP | GRCh38.p7 | 19:49560660 | TAGGTGTAGACGGCC[C/T]CTGCGGTGCAGTTCT | 51070 |
| rs764364369 | snp | C/T | 1.68607e-05 | 0.00290346 | missense | NOSIP | GRCh38.p7 | 19:49555816 | AGCCCGCGAAGCCGG[C/T]ACCGCCCTGGGGGAG | 51070 |
| rs764533959 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49570485 | AATGTATACACCCTT[A/G]TGACCACGACCCTAT | 51070 |
| rs764663766 | snp | C/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49571892 | CGGGAGGCTGAGGCA[C/G]AAGAATCGCTTGAAC | 51070 |
| rs764702712 | snp | C/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577425 | AGCTAGGCGTGGTAG[C/G]GCATGCCTGTAGCCC | 51070 |
| rs764747040 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49559254 | CCCAATAGAGCTGCA[A/G]GGAAAGTGCTTCATT | 51070 |
| rs764812182 | snp | C/T | 1.71091e-05 | 0.00292476 | intron-variant | NOSIP | GRCh38.p7 | 19:49556532 | TGGTCCCTTCCCTCC[C/T]CTCCCAGGTGACTCA | 51070 |
| rs764826192 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49578808 | CCTGCCATCATGCCC[A/G]GCTAAGGGGTTTCAC | 51070 |
| rs764930641 | snp | G/T | 1.7238e-05 | 0.00293576 | missense | NOSIP | GRCh38.p7 | 19:49556597 | CTCAGGCTGTCGCGG[G/T]TCACGGCACACACGT | 51070 |
| rs765015778 | snp | C/T | 0.000112244 | 0.00749062 | intron-variant | NOSIP | GRCh38.p7 | 19:49559897 | CGGTTCCCTTGCTCT[C/T]CCCACCCAGACCTAC | 51070 |
| rs765027612 | in-del | -/AAAA | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565762 | AACCTGTCTCAAAAG[-/AAAA]AAAAAAAAAAGAAAG | 51070 |
| rs765049931 | snp | A/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49566923 | AGGTTCAAGCAAATT[A/C]TCCTGCCTCAGCCTC | 51070 |
| rs765106549 | snp | A/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49568553 | TATCAACTGCATTGG[A/C]ATAAATTCACATTTT | 51070 |
| rs765221661 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576029 | AGTCCCAGCTACTCC[A/G]GAAGCTGAGGCAGGA | 51070 |
| rs765492626 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49572557 | AACTGGAATTCCAGG[C/T]GTGTGCCACCATGCC | 51070 |
| rs765495920 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49568940 | CCTGAGTAGCTGGGA[C/T]TACAGGCCTGCACCA | 51070 |
| rs765551872 | snp | A/G | 5.70304e-05 | 0.00533966 | intron-variant | NOSIP | GRCh38.p7 | 19:49556824 | TGAGGAGGACGGTGG[A/G]GAACCCTGGCGCCCT | 51070 |
| rs765556758 | snp | A/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49566690 | TGGGCTGAGTGCAGC[A/C]ATGTTTACAACTAAT | 51070 |
| rs765719587 | snp | C/T | 3.33929e-05 | 0.00408599 | missense | NOSIP | GRCh38.p7 | 19:49555756 | CCGCACACACTCAGG[C/T]CTGCATCACCGGCCG | 51070 |
| rs765728130 | snp | C/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49574319 | ACTCAAGACAAAAAC[C/G]AAATTATTCAGACTA | 51070 |
| rs765836266 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49558595 | GGACCTAAGCTACAG[A/G]GTGGGAAAACTCGAA | 51070 |
| rs765855612 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49563882 | TTTTAAACATTTCCC[A/G]TTGTTCCTAGGCTAT | 51070 |
| rs766173976 | snp | C/G | 3.42507e-05 | 0.00413814 | intron-variant | NOSIP | GRCh38.p7 | 19:49556544 | TCCCCTCCCAGGTGA[C/G]TCACGAGGGCCGCAG | 51070 |
| rs766324573 | in-del | -/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49558220 | GCCCAGAAAAAATGA[-/G]GTGATGTCAATTCAC | 51070 |
| rs766561412 | snp | A/C | 2.16574e-05 | 0.00329063 | missense | NOSIP | GRCh38.p7 | 19:49556967 | CCTTACTTGGAGGAC[A/C]CACACTGGGCCCAGG | 51070 |
| rs766573027 | snp | C/T | 3.2467e-05 | 0.00402895 | intron-variant | NOSIP | GRCh38.p7 | 19:49557049 | CCGCCCAGCCCGCGG[C/T]GCCCCGCCCCCCAAC | 51070 |
| rs766703222 | snp | C/T | 1.64808e-05 | 0.00287057 | missense | NOSIP | GRCh38.p7 | 19:49558907 | ATCACCTTCATCTGC[C/T]GGGCAATCTCCTTCT | 51070 |
| rs766703408 | snp | A/G | 5.08023e-05 | 0.0050397 | intron-variant | NOSIP | GRCh38.p7 | 19:49555832 | ACCGCCCTGGGGGAG[A/G]TAGAGAGAAGGACGA | 51070 |
| rs766818099 | snp | A/T | 1.65897e-05 | 0.00288003 | intron-variant | NOSIP | GRCh38.p7 | 19:49556285 | GGCGGGGCCTTGGAG[A/T]GCTGGGGGAAGGGGA | 51070 |
| rs766907529 | in-del | -/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49563182 | CGTTTTTTCTTTTTG[-/T]TTTTTTTTTTTGAGA | 51070 |
| rs767023635 | snp | G/T | 1.64814e-05 | 0.00287061 | missense | NOSIP | GRCh38.p7 | 19:49558916 | ATCTGCCGGGCAATC[G/T]CCTTCTTCTGGTGCA | 51070 |
| rs767140155 | snp | C/G | 5.56127e-05 | 0.00527288 | intron-variant | NOSIP | GRCh38.p7 | 19:49556290 | GGCCTTGGAGTGCTG[C/G]GGGAAGGGGAGGGGT | 51070 |
| rs767244251 | snp | C/T | | | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555325 | GTGCAATGGTGCGAT[C/T]TTGGCTCACTGCAAC | 51070 |
| rs767268699 | snp | A/G/T | 8.30246e-05 | 0.00644253 | intron-variant | NOSIP | GRCh38.p7 | 19:49559024 | GAAAGTGATCCTCCC[A/G/T]CCTCGGCCTCCCGAA | 51070 |
| rs767271460 | snp | A/G | 3.49412e-05 | 0.00417964 | missense | NOSIP | GRCh38.p7 | 19:49556625 | CGTAGCGCTCGCTGC[A/G]GGTGATGAGCCCCAC | 51070 |
| rs767361105 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565383 | GATCTGGGTGCTGGT[C/T]ACATGGGTGTGTTTG | 51070 |
| rs767394385 | snp | C/T | 3.20446e-05 | 0.00400266 | intron-variant | NOSIP | GRCh38.p7 | 19:49556779 | AGTAGGCAGGGCTGG[C/T]GCAGGTGGAGAGCGC | 51070 |
| rs767622716 | in-del | -/CT | | | intron-variant | NOSIP | GRCh38.p7 | 19:49559502 | GCAACAAAGTGAAGA[-/CT]CTGTCTCAAAAAAAA | 51070 |
| rs767674972 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49559589 | AAAATATACCACTAA[C/T]TGAGCACGTATTTAG | 51070 |
| rs767677003 | snp | C/T | 3.11473e-05 | 0.00394622 | intron-variant | NOSIP | GRCh38.p7 | 19:49557057 | CCCGCGGCGCCCCGC[C/T]CCCCAACCCACAAGA | 51070 |
| rs767684564 | snp | A/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49571775 | GTGGATCACAAGGTC[A/C]AGATGTTGAGACCAT | 51070 |
| rs767747125 | in-del | -/AGAA | 0.000165551 | 0.00909659 | intron-variant | NOSIP | GRCh38.p7 | 19:49558999 | AGACAGGGTGCAATG[-/AGAA]AGAAAGAAAGAAAGT | 51070 |
| rs767763627 | in-del | -/TATG | | | intron-variant | NOSIP | GRCh38.p7 | 19:49573798 | TTTATTTTATGTATG[-/TATG]TATGTATGTATGTAT | 51070 |
| rs767795573 | snp | C/T | 2.12895e-05 | 0.00326256 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555668 | GCATCCTCGCCTGCC[C/T]TGTCCCCGGGGCGCC | 51070 |
| rs767839416 | snp | C/T | 3.98502e-05 | 0.00446357 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555689 | CCGGGGCGCCCACGC[C/T]GCGAATGAAGGCGCC | 51070 |
| rs767900611 | snp | C/T | 0.000102617 | 0.00716225 | missense | NOSIP | GRCh38.p7 | 19:49556370 | CTCCAGTCACAGGGT[C/T]CACCATGTCCTTCCG | 51070 |
| rs767958854 | in-del | -/AG | | | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49578670 | TTTTTTTTTTGAGAC[-/AG]AGTCTCACTCTGTCG | 51070 |
| rs767979826 | in-del | -/TG | | | intron-variant | NOSIP | GRCh38.p7 | 19:49567322 | GAAACGGGTTTTCAC[-/TG]TGTTAGCCAGGATGG | 51070 |
| rs768200508 | snp | C/G | 2.39426e-05 | 0.00345988 | missense | NOSIP | GRCh38.p7 | 19:49556991 | GCCCAGGTTGGACAT[C/G]ATCTGTGGGGGAAGG | 51070 |
| rs768342574 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49571822 | AAACCCCATCTCTAC[C/T]AAAAATACAAAAATT | 51070 |
| rs768366062 | snp | C/T | 1.75167e-05 | 0.0029594 | missense | NOSIP | GRCh38.p7 | 19:49559992 | AGTCGAAGTCCTTCA[C/T]GGCATCCCGGCTCAG | 51070 |
| rs768439156 | snp | C/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49560960 | GAGGGTGAGAGACCA[C/G]AGTTCAAATTCTAGC | 51070 |
| rs768477864 | snp | A/G | 4.35531e-05 | 0.00466633 | missense | NOSIP | GRCh38.p7 | 19:49557104 | CCTGGGCTGGTGCCC[A/G]AGAGGGCCTTGGCTG | 51070 |
| rs768488927 | snp | C/G | 7.75164e-05 | 0.00622512 | intron-variant | NOSIP | GRCh38.p7 | 19:49560588 | GACTCCAAGACACAG[C/G]CATGTCCCGCCTCTT | 51070 |
| rs768587376 | snp | G/T | 3.17758e-05 | 0.00398584 | intron-variant | NOSIP | GRCh38.p7 | 19:49557041 | CCCTGGGCCCGCCCA[G/T]CCCGCGGCGCCCCGC | 51070 |
| rs768749037 | snp | C/G | 3.30584e-05 | 0.00406548 | missense | NOSIP | GRCh38.p7 | 19:49557208 | CGCCCGCTGAAGCTC[C/G]TTCTGCTCCTCGCGC | 51070 |
| rs768766004 | snp | A/G | 1.76359e-05 | 0.00296945 | intron-variant | NOSIP | GRCh38.p7 | 19:49555863 | GGTAGAGGCCGGCCC[A/G]GGGGTGACCAGTGGG | 51070 |
| rs768886022 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575502 | GGGGCACCCAGGCAG[C/T]ATGCAACATGAAGCG | 51070 |
| rs768943864 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565883 | GCTACAGATTCATCC[C/T]TGAATGAACACAACT | 51070 |
| rs768969666 | snp | C/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575872 | CGCAGTGGCTCACGC[C/G]TGTAATCCCAGCACT | 51070 |
| rs768998032 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | PRRG2, NOSIP | GRCh38.p7 | 19:49580670 | TGCCTCGCCTGGCTT[C/G]CTCAAGTCCTCTCTT | 51070 |
| rs769018498 | in-del | -/AG | 0.444444 | 0.157135 | intron-variant | NOSIP | GRCh38.p7 | 19:49556748 | GGGACTGCAAGGGGC[-/AG]AGAGAGGCGGGCTCA | 51070 |
| rs769055597 | snp | A/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564689 | TTCGTCTCCCACGTA[A/T]ACACCTAACAGAAGG | 51070 |
| rs769158626 | snp | G/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565625 | TTGCTGGGTGTGGTG[G/T]CACACGCCTGTAATC | 51070 |
| rs769242681 | snp | A/G | 1.93575e-05 | 0.00311101 | missense | NOSIP | GRCh38.p7 | 19:49556702 | TCCGACATGCGCAGG[A/G]GCTTCCCTGACATGG | 51070 |
| rs769306276 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49566106 | CTCAGTGCAACCTCT[A/G]CCACCCGGGTTCACG | 51070 |
| rs769389639 | in-del | -/A | 4.25999e-05 | 0.00461499 | frameshift-variant | NOSIP | GRCh38.p7 | 19:49557146 | AGGGGCCGGCTCACG[-/A]TAGCCGACTCCTTCT | 51070 |
| rs769441938 | snp | C/T | 0.000131182 | 0.00809776 | intron-variant | NOSIP | GRCh38.p7 | 19:49560726 | TGGCAGGACTGTGGT[C/T]ACCGGAGGCAGGCAG | 51070 |
| rs769578558 | snp | A/G | 2.02263e-05 | 0.00318006 | missense | NOSIP | GRCh38.p7 | 19:49556723 | CCTGACATGGGGCAG[A/G]TCACCGTGCGGGACT | 51070 |
| rs769613583 | snp | A/C/G | 0.000123825 | 0.00786765 | missense, synonymous-codon | NOSIP | GRCh38.p7 | 19:49557127 | CTTGGCTGTGAAAGG[A/C/G]TTGAGGGGCCGGCTC | 51070 |
| rs769628946 | snp | C/T | 3.37154e-05 | 0.00410568 | missense | NOSIP | GRCh38.p7 | 19:49555798 | CTTGCAGCTTCACTC[C/T]GGAGCCCGCGAAGCC | 51070 |
| rs769752004 | snp | C/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49559660 | AGAGGTAGGTCATGG[C/G]AAGTGTCCAAAGGTG | 51070 |
| rs769802587 | in-del | -/CCTT | | | intron-variant | NOSIP | GRCh38.p7 | 19:49570513 | TATGGAGATACAGAA[-/CCTT]CCTATCACGCTAAAT | 51070 |
| rs769816512 | snp | A/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49569982 | CCAGTCGTGGTGGCC[A/C]CCTGTAATCCCAGCT | 51070 |
| rs769816516 | snp | A/G | 4.91232e-05 | 0.00495572 | missense | NOSIP | GRCh38.p7 | 19:49557174 | TCTCCAGGAAGCCCC[A/G]CACATGGTCCTGCGA | 51070 |
| rs769838519 | snp | A/G | 1.65767e-05 | 0.00287891 | intron-variant | NOSIP | GRCh38.p7 | 19:49559015 | AGAAAGAAAGAAAGT[A/G]ATCCTCCCGCCTCGG | 51070 |
| rs769867919 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49571311 | TTTTTAAAACTCAGT[A/G]ATTTTTAAGATCCTG | 51070 |
| rs769870703 | snp | C/T | 3.71872e-05 | 0.00431187 | missense | NOSIP | GRCh38.p7 | 19:49556334 | GCTGCAGCACGATGA[C/T]GTCGCGGTCTGTGAG | 51070 |
| rs769904794 | snp | A/C | | | intron-variant, utr-variant-5-prime | NOSIP | GRCh38.p7 | 19:49576822 | CTGGGAGGCGAAGGT[A/C]GTGATGAGCCAAGAT | 51070 |
| rs769958131 | snp | A/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49561212 | CTGCCTGCCAGTCCA[A/C]TAGCGACTGGATCTA | 51070 |
| rs769959838 | in-del | -/AAC | | | intron-variant | NOSIP | GRCh38.p7 | 19:49569821 | TCAAAAAACAAAAAC[-/AAC]AACAACAACAACAAC | 51070 |
| rs770143835 | in-del | -/TGTTGGCCAGGCTGGCC | | | intron-variant | NOSIP | GRCh38.p7 | 19:49558460 | GACAGGGTTTCACCA[-/TGTTGGCCAGGCTGGCC]TCTAACTGTTGACCT | 51070 |
| rs770210878 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575694 | ACTCCACTCAGCCCC[C/T]GTAGCATAAAAGCAG | 51070 |
| rs770273311 | snp | A/G | 1.84154e-05 | 0.00303436 | intron-variant | NOSIP | GRCh38.p7 | 19:49556867 | GCCGGGGCGCTGTGG[A/G]GGCTCACCGGCTTCT | 51070 |
| rs770327606 | snp | A/C | 2.11835e-05 | 0.00325443 | missense | NOSIP | GRCh38.p7 | 19:49556732 | GGGCAGGTCACCGTG[A/C]GGGACTGCAAGGGGC | 51070 |
| rs770349642 | snp | A/G | 3.29669e-05 | 0.00405984 | intron-variant | NOSIP | GRCh38.p7 | 19:49558875 | CTGCCTCCGTGTGCC[A/G]CCTCCTCCCCATCCC | 51070 |
| rs770354102 | in-del | -/G | 2.12592e-05 | 0.00326024 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555676 | GCCTGCCCTGTCCCC[-/G]GGGCGCCCACGCCGC | 51070 |
| rs770454476 | snp | C/T | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579612 | CTCTGAAAACAACCT[C/T]TGCTCAGCTCATCGG | 51070 |
| rs770579527 | snp | C/T | 1.84606e-05 | 0.00303808 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49556875 | GCTGTGGGGGCTCAC[C/T]GGCTTCTCCAGCTTG | 51070 |
| rs770607837 | in-del | -/GGAA | 2.52742e-05 | 0.00355478 | intron-variant | NOSIP | GRCh38.p7 | 19:49557001 | GACATCATCTGTGGG[-/GGAA]GGAAGGGACTCAGAT | 51070 |
| rs770771042 | snp | A/C | | | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49582482 | AAAATGAGTTGAGGC[A/C]GGGCACAGTGGCTCA | 51070 |
| rs770774515 | in-del | -/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49569838 | CAACAACAACAACAA[-/C]AAAAGAACACTTGCA | 51070 |
| rs770799889 | snp | G/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49573426 | ACAGCCCGTCCCTCG[G/T]TATTTCGGCTCCAGA | 51070 |
| rs770835468 | snp | A/C | 1.6918e-05 | 0.00290839 | missense | NOSIP | GRCh38.p7 | 19:49555807 | TCACTCCGGAGCCCG[A/C]GAAGCCGGTACCGCC | 51070 |
| rs770837422 | snp | A/G | 0.000147471 | 0.00858567 | intron-variant | NOSIP | GRCh38.p7 | 19:49557273 | GGGAAAGTGGGCTGA[A/G]CATCTGCCCGTGGGG | 51070 |
| rs770888757 | snp | A/C/T | 5.25945e-05 | 0.00512786 | intron-variant | NOSIP | GRCh38.p7 | 19:49555860 | CGAGGTAGAGGCCGG[A/C/T]CCGGGGGTGACCAGT | 51070 |
| rs770924214 | in-del | -/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49566818 | TATACACACATACTA[-/T]TTTTTTTTTTTTTTT | 51070 |
| rs770951202 | snp | A/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49557546 | TACCCACCTCAGCGG[A/C]TCACTGAAGGGTTAC | 51070 |
| rs770999602 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49568696 | ATGCCTGTAATCCCA[A/G]CACTTTGGGAAACCA | 51070 |
| rs771109884 | in-del | -/T | | | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49578652 | TCTATCTATTTTTTC[-/T]TTTTTTTTTTTTGAG | 51070 |
| rs771296306 | snp | C/T | 1.65974e-05 | 0.0028807 | intron-variant | NOSIP | GRCh38.p7 | 19:49559022 | AAGAAAGTGATCCTC[C/T]CGCCTCGGCCTCCCG | 51070 |
| rs771428805 | snp | A/G | 0.000197463 | 0.00993442 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49556341 | CACGATGATGTCGCG[A/G]TCTGTGAGTTTGTCT | 51070 |
| rs771520943 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49568208 | TAAGACATACCAACA[C/T]ACTCCAAAAATATGG | 51070 |
| rs771615227 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49558782 | GGAAGCAGGGGAGGG[A/G]AATGGTGTACCAGGC | 51070 |
| rs771637719 | snp | C/G/T | 5.88395e-05 | 0.00542373 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555691 | GGGGCGCCCACGCCG[C/G/T]GAATGAAGGCGCCAC | 51070 |
| rs771700754 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49557813 | CAGCAGTTGCCTGGG[C/T]GGTGCTGCAGTTCCA | 51070 |
| rs771847643 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575268 | CCTCCCACAGTGCTG[A/G]GATTATAGGCATGAG | 51070 |
| rs771889659 | snp | C/T | 4.97946e-05 | 0.00498947 | intron-variant | NOSIP | GRCh38.p7 | 19:49556314 | GAGGGGTGGGACTCT[C/T]ACCCGCTGCAGCACG | 51070 |
| rs771926441 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49559434 | GAGGCAGGAGGATCA[C/T]CTGAGCCTGGGATAT | 51070 |
| rs771996511 | snp | G/T | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579497 | CACCTGATAAAGGAA[G/T]TCCCCTCTACTTTAA | 51070 |
| rs772064230 | snp | A/G | 1.84589e-05 | 0.00303794 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49556920 | GGGCGTCAGCGACGG[A/G]ATCCAGAAGCTGGGC | 51070 |
| rs772302123 | snp | C/T | 1.83488e-05 | 0.00302887 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49559957 | AGGATCGTGGCAAGG[C/T]TGCAGGGAGAGACAA | 51070 |
| rs772360990 | snp | C/G | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579341 | GATTGAGCTCCTGCA[C/G]TAGGTTCAACAGACC | 51070 |
| rs772372595 | snp | C/T | 4.20292e-05 | 0.00458397 | missense | NOSIP | GRCh38.p7 | 19:49557137 | AAAGGGTTGAGGGGC[C/T]GGCTCACGATAGCCG | 51070 |
| rs772418014 | snp | G/T | 0.000238818 | 0.0109248 | intron-variant | NOSIP | GRCh38.p7 | 19:49556508 | CGGACCGCCCCGCAG[G/T]TTCCCGAGTGGTCCC | 51070 |
| rs772430481 | snp | C/G | 0.000114692 | 0.00757185 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49557190 | CACATGGTCCTGCGA[C/G]GCCGCCCGCTGAAGC | 51070 |
| rs772465910 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49578751 | TCCCGGGTTCACGCA[A/G]TTCTCCTGCCTCAGC | 51070 |
| rs772474892 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564311 | TACAAAAAGTTAGCT[A/G]GTCGTGGTGGTGTGC | 51070 |
| rs772580114 | snp | A/C | 0.0002945 | 0.0121311 | intron-variant | NOSIP | GRCh38.p7 | 19:49560081 | GGAGGGGCGGAGCAA[A/C]AGGAGACATGTCCGT | 51070 |
| rs772601944 | snp | C/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49562972 | TCTCCCAAGCTTAAA[C/G]AGTTGCAAAGGATAC | 51070 |
| rs772613732 | snp | C/T | 6.83597e-05 | 0.00584595 | intron-variant | NOSIP | GRCh38.p7 | 19:49560729 | CAGGACTGTGGTTAC[C/T]GGAGGCAGGCAGCAC | 51070 |
| rs772637224 | snp | C/T | 1.71746e-05 | 0.00293036 | missense | NOSIP | GRCh38.p7 | 19:49556579 | GCGCAGGGGGTGGCG[C/T]TGCTCAGGCTGTCGC | 51070 |
| rs772788289 | snp | C/T | 3.45328e-05 | 0.00415514 | missense | NOSIP | GRCh38.p7 | 19:49556601 | GGCTGTCGCGGGTCA[C/T]GGCACACACGTAGCG | 51070 |
| rs772852060 | snp | C/T | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579501 | TGATAAAGGAAGTCC[C/T]CTCTACTTTAACCTT | 51070 |
| rs772903062 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564736 | GACACATACACTGCC[C/T]TATTCACAATGGCTC | 51070 |
| rs773083998 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49570188 | TGCATTCAGGAAAGA[C/T]TGTCTCCTGCTCTCA | 51070 |
| rs773197628 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49561251 | GATTATGTCTCAGAT[C/T]GACCGATCAGAGGGC | 51070 |
| rs773298711 | snp | A/C | 1.81464e-05 | 0.00301212 | missense | NOSIP | GRCh38.p7 | 19:49556339 | AGCACGATGATGTCG[A/C]GGTCTGTGAGTTTGT | 51070 |
| rs773311071 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49566382 | GGTACAATCATAGCT[C/T]GCTGCAGCCTCAAAC | 51070 |
| rs773635699 | snp | C/T | 0.000154895 | 0.00879905 | intron-variant | NOSIP | GRCh38.p7 | 19:49556280 | GGAGGGGCGGGGCCT[C/T]GGAGTGCTGGGGGAA | 51070 |
| rs773691874 | snp | G/T | 3.2963e-05 | 0.00405961 | intron-variant | NOSIP | GRCh38.p7 | 19:49558878 | CCTCCGTGTGCCGCC[G/T]CCTCCCCATCCCCAT | 51070 |
| rs773752957 | snp | A/G | 1.65784e-05 | 0.00287905 | intron-variant | NOSIP | GRCh38.p7 | 19:49559016 | GAAAGAAAGAAAGTG[A/G]TCCTCCCGCCTCGGC | 51070 |
| rs773758100 | snp | C/T | 0.00276977 | 0.0371108 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49556881 | GGGGCTCACCGGCTT[C/T]TCCAGCTTGGTGGCC | 51070 |
| rs773820122 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49559702 | TGGCCTCGGCAATGC[C/T]CTGAGAGCCCTACAC | 51070 |
| rs773874012 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564966 | TTCAAAAACTCACAA[A/G]GTAATTACTACACCA | 51070 |
| rs773926907 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49566388 | ATCATAGCTCGCTGC[A/G]GCCTCAAACTCCTGG | 51070 |
| rs773936403 | snp | A/G | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580992 | TTGAAAATCAAAGCC[A/G]TTCAAGTCGCTCTCA | 51070 |
| rs773998497 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49581561 | TCCGAGACCCAGAAG[-/TT]TGGGGCTCCTAGGCC | 51070 |
| rs774144400 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49557698 | GGGGGATGTAGACTT[C/T]AGATCTAAGGGAATG | 51070 |
| rs774195777 | snp | C/T | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579648 | TCACGCTATTTTCCA[C/T]AATTAGATGTTGTTT | 51070 |
| rs774254385 | snp | G/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576005 | CCGGGCGTGGTGGCG[G/T]GCGCCTGTAGTCCCA | 51070 |
| rs774259604 | snp | A/G | 1.69367e-05 | 0.00290999 | intron-variant | NOSIP | GRCh38.p7 | 19:49560732 | GACTGTGGTTACCGG[A/G]GGCAGGCAGCACAGG | 51070 |
| rs774329916 | in-del | -/AG | | | intron-variant | NOSIP | GRCh38.p7 | 19:49568797 | AAAAAAAAAAAAAAT[-/AG]TTTGTTTGTTTGTTT | 51070 |
| rs774388893 | snp | A/G | 0.000142542 | 0.008441 | intron-variant | NOSIP | GRCh38.p7 | 19:49556756 | AAGGGGCAGAGAGAG[A/G]CGGGCTCAGTAGGCA | 51070 |
| rs774682615 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49571478 | GACTGCTGCCATCTG[C/T]TGTCACCAGCATTTC | 51070 |
| rs774706194 | snp | G/T | 0.000225265 | 0.0106105 | intron-variant | NOSIP | GRCh38.p7 | 19:49557055 | AGCCCGCGGCGCCCC[G/T]CCCCCCAACCCACAA | 51070 |
| rs774833205 | snp | G/T | 1.75915e-05 | 0.00296571 | missense | NOSIP | GRCh38.p7 | 19:49556349 | TGTCGCGGTCTGTGA[G/T]TTTGTCTCCAGTCAC | 51070 |
| rs774876103 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577157 | CCCTTATACATTGGT[A/G]GTAGAAATGTAAAAT | 51070 |
| rs774886527 | snp | A/G | 1.70563e-05 | 0.00292025 | intron-variant | NOSIP | GRCh38.p7 | 19:49556499 | CCCCAAAGCCGGACC[A/G]CCCCGCAGGTTCCCG | 51070 |
| rs775053930 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49562828 | CAGGTTGCAGGGAGT[A/G]GAGATTGCACCACTA | 51070 |
| rs775141887 | snp | C/T | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580375 | GCTTCAAACTTGGGG[C/T]GCCCGGACAGCTGTA | 51070 |
| rs775323843 | snp | C/T | 1.75631e-05 | 0.00296332 | missense | NOSIP | GRCh38.p7 | 19:49559980 | AGAGACAACAGCAGT[C/T]GAAGTCCTTCACGGC | 51070 |
| rs775562171 | in-del | -/GA | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580290 | GACTGAGTTTATAGT[-/GA]GAGAGAGAGACAAAG | 51070 |
| rs775591748 | in-del | -/CCAGGAAGC | 2.19051e-05 | 0.00330939 | cds-indel | NOSIP | GRCh38.p7 | 19:49557155 | TCACGATAGCCGACT[-/CCAGGAAGC]CCTTCTCCAGGAAGC | 51070 |
| rs775620713 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49574110 | TCAGGTGATCTACTA[C/T]CTCGGCCTCCCAAAG | 51070 |
| rs775632337 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49571466 | AACTACAAAGCAGAC[C/T]GCTGCCATCTGCTGT | 51070 |
| rs775704908 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49557869 | TGAGGAGGTAACAGT[A/G]ACAGTGATGGATGCT | 51070 |
| rs775726917 | snp | A/G | 2.10458e-05 | 0.00324383 | missense | NOSIP | GRCh38.p7 | 19:49557138 | AAGGGTTGAGGGGCC[A/G]GCTCACGATAGCCGA | 51070 |
| rs775828579 | snp | A/G | | | missense | NOSIP | GRCh38.p7 | 19:49555771 | CCTGCATCACCGGCC[A/G]TGATTTCTCCGCTTG | 51070 |
| rs775851227 | snp | C/T | 2.94131e-05 | 0.0038348 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49557193 | ATGGTCCTGCGAGGC[C/T]GCCCGCTGAAGCTCC | 51070 |
| rs775855155 | snp | C/T | 1.72116e-05 | 0.00293351 | missense | NOSIP | GRCh38.p7 | 19:49556588 | GTGGCGTTGCTCAGG[C/T]TGTCGCGGGTCACGG | 51070 |
| rs775904295 | snp | C/G | 5.05582e-05 | 0.00502758 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49555811 | TCCGGAGCCCGCGAA[C/G]CCGGTACCGCCCTGG | 51070 |
| rs775979942 | snp | A/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49561921 | TGCCTAAGCCAAGAT[A/T]ATGCACATTTATTCC | 51070 |
| rs776003625 | snp | C/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564599 | TCAGGGGAGTGCAGA[C/G]CAGCACAACCACTTT | 51070 |
| rs776057381 | in-del | -/TGG | 0.000439444 | 0.0148165 | cds-indel | NOSIP | GRCh38.p7 | 19:49557095 | CTGAGTCACCTGGGC[-/TGG]TGGTGCCCGAGAGGG | 51070 |
| rs776203889 | in-del | -/G | 0.000101071 | 0.00710813 | utr-variant-3-prime | NOSIP | GRCh38.p7 | 19:49555731 | ACCCAAGCCGGTTTA[-/G]TTTGGTCTCCCGCAC | 51070 |
| rs776300944 | snp | G/T | 1.66899e-05 | 0.00288871 | intron-variant | NOSIP | GRCh38.p7 | 19:49557045 | GGGCCCGCCCAGCCC[G/T]CGGCGCCCCGCCCCC | 51070 |
| rs776338954 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577391 | GCGAAACCCCATCTC[C/T]ACTAAAAATACAAAA | 51070 |
| rs776406609 | snp | C/G | 1.67514e-05 | 0.00289403 | intron-variant | NOSIP | GRCh38.p7 | 19:49560594 | AAGACACAGCCATGT[C/G]CCGCCTCTTCCCACC | 51070 |
| rs776411101 | snp | C/G | 1.71056e-05 | 0.00292446 | intron-variant | NOSIP | GRCh38.p7 | 19:49556521 | AGGTTCCCGAGTGGT[C/G]CCTTCCCTCCCCTCC | 51070 |
| rs776444209 | snp | C/T | 4.15239e-05 | 0.00455634 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49556959 | GTCCTTGTCCTTACT[C/T]GGAGGACCCACACTG | 51070 |
| rs776460161 | snp | A/G | 5.1721e-05 | 0.00508506 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49556593 | GTTGCTCAGGCTGTC[A/G]CGGGTCACGGCACAC | 51070 |
| rs776532299 | snp | C/T | 3.36434e-05 | 0.00410129 | missense | NOSIP | GRCh38.p7 | 19:49557210 | CCCGCTGAAGCTCCT[C/T]CTGCTCCTCGCGCCG | 51070 |
| rs776589503 | snp | A/G | 1.68852e-05 | 0.00290557 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49555820 | CGCGAAGCCGGTACC[A/G]CCCTGGGGGAGGTAG | 51070 |
| rs776603339 | snp | C/T | 1.8936e-05 | 0.00307695 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555695 | CGCCCACGCCGCGAA[C/T]GAAGGCGCCACGTCG | 51070 |
| rs776619966 | in-del | -/CA | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564782 | CCCCATGCCTGTCAG[-/CA]CAGAGTAGATAAAGA | 51070 |
| rs776622991 | snp | C/T | 4.14353e-05 | 0.00455148 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49557112 | GGTGCCCGAGAGGGC[C/T]TTGGCTGTGAAAGGG | 51070 |
| rs776791602 | snp | G/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49568756 | TCAAGACCAGCCTGG[G/T]CAATATAGCTAGACC | 51070 |
| rs776825041 | in-del | -/CATGTTGGCCAGGCTGGT | | | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555458 | GAGACAAGGTTTCAC[-/CATGTTGGCCAGGCTGGT]CTCGAACTCCTGACC | 51070 |
| rs776826256 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49559608 | GCACGTATTTAGTGC[C/T]TGGACTCAGCACCTG | 51070 |
| rs777030068 | snp | C/T | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49581200 | ATCCCCCAGGTATCC[C/T]ATGGTATTCGACACC | 51070 |
| rs777226139 | snp | C/T | | | missense | NOSIP | GRCh38.p7 | 19:49560655 | CGTGGTAGGTGTAGA[C/T]GGCCCCTGCGGTGCA | 51070 |
| rs777239097 | snp | G/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49574244 | ACAAACCAGCCTCAG[G/T]GGGGCTTTTCAGAAT | 51070 |
| rs777369364 | in-del | -/AAT | | | intron-variant | NOSIP | GRCh38.p7 | 19:49564117 | GTAATTTGTTACAAC[-/AAT]GATAGGAAACTAATA | 51070 |
| rs777451837 | snp | C/T | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580812 | TTTTCCTGCTTGGTT[C/T]CCAGGTTTTGAGTCT | 51070 |
| rs777545441 | snp | A/C | 1.6604e-05 | 0.00288127 | intron-variant | NOSIP | GRCh38.p7 | 19:49559026 | AAGTGATCCTCCCGC[A/C]TCGGCCTCCCGAAGT | 51070 |
| rs777824901 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49573347 | TGCCTCCTCCAAGAA[A/G]CCTGCCTCTCCGGGA | 51070 |
| rs777856646 | snp | C/T | 2.56987e-05 | 0.00358451 | intron-variant | NOSIP | GRCh38.p7 | 19:49559924 | CTACCCATCCCTGTT[C/T]CCAGCTCACGTGACA | 51070 |
| rs777908323 | snp | A/G | 2.22457e-05 | 0.00333502 | intron-variant | NOSIP | GRCh38.p7 | 19:49560071 | GCAGAGTGATGGAGG[A/G]GCGGAGCAACAGGAG | 51070 |
| rs777923016 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49564087 | GAGGTGTGACACTGC[A/G]ACACTAAATTAGTAG | 51070 |
| rs777934946 | in-del | -/A | | | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49579296 | CACACGCACCCTGTT[-/A]GATAAAATTTATAGA | 51070 |
| rs778031868 | snp | C/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49557000 | GGACATCATCTGTGG[C/G]GGAAGGAAGGGACTC | 51070 |
| rs778081799 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NOSIP, PRRG2 | GRCh38.p7 | 19:49579239 | TTCTTTTAAAGTGTG[A/G]TGATGGTATTGTGGT | 51070 |
| rs778260941 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49560165 | CTCAGAGAGAAACAG[A/G]CAGTTGGGAGCCGCT | 51070 |
| rs778360862 | snp | C/T | | | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49581833 | TGCTTTCTTCTCTGG[C/T]GGACACTGCCTTCAC | 51070 |
| rs778490568 | snp | C/G | 2.11616e-05 | 0.00325274 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555674 | TCGCCTGCCCTGTCC[C/G]CGGGGCGCCCACGCC | 51070 |
| rs778604132 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49573480 | CTGGGTTGAACTTCA[A/G]CCTGGGTCCCAGCAT | 51070 |
| rs778662088 | snp | C/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576238 | TGTGGCTCATACCTG[C/G]ATAGGGTGCTTTGGG | 51070 |
| rs778790721 | snp | A/G | 1.65509e-05 | 0.00287666 | intron-variant | NOSIP | GRCh38.p7 | 19:49558996 | GCAAAGACAGGGTGC[A/G]ATGAGAAAGAAAGAA | 51070 |
| rs778892261 | snp | C/T | 4.62332e-05 | 0.00480775 | missense | NOSIP | GRCh38.p7 | 19:49560675 | CCTGCGGTGCAGTTC[C/T]TGCCATGCCGCGTCA | 51070 |
| rs778917118 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49559176 | AGATTAAAATCAGCA[A/G]AGGAAAAAGGCACAT | 51070 |
| rs779040890 | snp | C/T | 3.55676e-05 | 0.00421693 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49556647 | GAGCCCCACGCGGTC[C/T]ACGGAGCTGTCTAGC | 51070 |
| rs779054554 | snp | A/G | 1.69986e-05 | 0.0029153 | missense | NOSIP | GRCh38.p7 | 19:49556409 | TCTCCACGCATTCGA[A/G]GGTGACCACAGCCCC | 51070 |
| rs779102066 | snp | C/T | | | intron-variant, utr-variant-5-prime | NOSIP | GRCh38.p7 | 19:49564223 | CTTTGGAGGCTGAAG[C/T]GGGCAGATCACTTGA | 51070 |
| rs779180325 | in-del | -/CCCTGGCG | 0.000152326 | 0.00872581 | intron-variant | NOSIP | GRCh38.p7 | 19:49556828 | GAGGACGGTGGGGAA[-/CCCTGGCG]CCCTGGCACCGTGCG | 51070 |
| rs779224510 | snp | C/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565628 | CTGGGTGTGGTGGCA[C/G]ACGCCTGTAATCCCA | 51070 |
| rs779285289 | snp | C/T | 7.73709e-05 | 0.00621928 | missense | NOSIP | GRCh38.p7 | 19:49559947 | ACGTGACAACAGGAT[C/T]GTGGCAAGGCTGCAG | 51070 |
| rs779292378 | snp | A/T | | | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555117 | TTCAAACCTGGCAAA[A/T]ATCCGGGAACCCTAA | 51070 |
| rs779342579 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49579311 | AGATAAAATTTATAG[A/G]AGGTCATTGGTTTGG | 51070 |
| rs779473110 | in-del | -/TT | | | intron-variant | NOSIP | GRCh38.p7 | 19:49572406 | TCACTGCACCCAGCC[-/TT]TTTTTTTTTTTTTTT | 51070 |
| rs779512621 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49569871 | TGGGGCGAGGTGGCT[C/T]ATGCCTGAGGTGAGC | 51070 |
| rs779524635 | snp | C/G/T | 2.36225e-05 | 0.00343667 | intron-variant | NOSIP | GRCh38.p7 | 19:49560075 | AGTGATGGAGGGGCG[C/G/T]AGCAACAGGAGACAT | 51070 |
| rs779613179 | snp | A/T | 4.34358e-05 | 0.00466004 | missense | NOSIP | GRCh38.p7 | 19:49557153 | GGCTCACGATAGCCG[A/T]CTCCTTCTCCAGGAA | 51070 |
| rs779819318 | snp | A/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49570617 | TGATCAAACACCCCA[A/C]CTTGACCCAGGGTCC | 51070 |
| rs779933869 | snp | C/T | 1.71032e-05 | 0.00292426 | intron-variant | NOSIP | GRCh38.p7 | 19:49556438 | CCACTACGGTGAGGC[C/T]GAAGGCGGGAGACTC | 51070 |
| rs780026225 | snp | C/G | 1.89106e-05 | 0.00307489 | intron-variant | NOSIP | GRCh38.p7 | 19:49556846 | TGGCGCCCTGGCACC[C/G]TGCGTGCCGGGGCGC | 51070 |
| rs780047341 | in-del | -/GTCC | 2.65837e-05 | 0.0036457 | intron-variant | NOSIP | GRCh38.p7 | 19:49560091 | AGCAACAGGAGACAT[-/GTCC]GTCTCCAAAGCCCCA | 51070 |
| rs780153499 | snp | A/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49567661 | ACAAGGGACTAATAT[A/C]ATTTTCATTTTTATT | 51070 |
| rs780178647 | snp | C/T | 1.70662e-05 | 0.00292109 | intron-variant | NOSIP | GRCh38.p7 | 19:49557282 | GGCTGAGCATCTGCC[C/T]GTGGGGCTGGGGGTA | 51070 |
| rs780361501 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | PRRG2, NOSIP | GRCh38.p7 | 19:49580558 | GCTTCTTCAACTGTG[C/T]CCCGACACCGGAAAG | 51070 |
| rs780566627 | in-del | -/CTC | 3.42369e-05 | 0.0041373 | intron-variant | NOSIP | GRCh38.p7 | 19:49556539 | TCCCTCCCCTCCCAG[-/CTC]GTGACTCACGAGGGC | 51070 |
| rs780577591 | snp | A/G | 2.48364e-05 | 0.00352386 | intron-variant | NOSIP | GRCh38.p7 | 19:49560083 | AGGGGCGGAGCAACA[A/G]GAGACATGTCCGTCT | 51070 |
| rs780594414 | snp | A/G | 1.6696e-05 | 0.00288924 | missense | NOSIP | GRCh38.p7 | 19:49555782 | GGCCGTGATTTCTCC[A/G]CTTGCAGCTTCACTC | 51070 |
| rs780658210 | snp | A/G | 0.0001114 | 0.00746241 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49556677 | CGGTGTGAAGTGCAC[A/G]GGCGTCAGGTCCGAC | 51070 |
| rs780692498 | snp | C/T | | | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555405 | CTGGGAATACAAGTG[C/T]GCACCACCATGCCCG | 51070 |
| rs780836275 | snp | A/G | 1.69954e-05 | 0.00291503 | intron-variant | NOSIP | GRCh38.p7 | 19:49555837 | CCTGGGGGAGGTAGA[A/G]AGAAGGACGAGGTAG | 51070 |
| rs780882340 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49571045 | GCAGTGGTGTGATCT[C/T]GGCTCACTGCAACCT | 51070 |
| rs780935407 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49568180 | GAGAACAGTTTCACA[C/T]GGGCTAGGTGGTTAA | 51070 |
| rs780937363 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49573183 | GTGTTTGATCCAAGC[A/G]CCTGTGGCTTTGACC | 51070 |
| rs781185665 | in-del | -/C | 1.70822e-05 | 0.00292247 | intron-variant | NOSIP | GRCh38.p7 | 19:49556504 | AGCCGGACCGCCCCG[-/C]CAGGTTCCCGAGTGG | 51070 |
| rs781263509 | snp | A/G | 1.65663e-05 | 0.002878 | intron-variant | NOSIP | GRCh38.p7 | 19:49559009 | GCAATGAGAAAGAAA[A/G]AAAGTGATCCTCCCG | 51070 |
| rs781321147 | snp | A/G | 3.85052e-05 | 0.00438761 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49556329 | TACCCGCTGCAGCAC[A/G]ATGATGTCGCGGTCT | 51070 |
| rs781412238 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576682 | CTGAGGTTGGGAATT[C/T]GAGACCAGCCTGACC | 51070 |
| rs781518095 | snp | A/C | | | missense | NOSIP | GRCh38.p7 | 19:49556555 | GTGACTCACGAGGGC[A/C]GCAGCACAGCGCAGG | 51070 |
| rs781534464 | in-del | -/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49568779 | CTAGACCCCATCTCT[-/T]AAAAAAAAAAAAAAA | 51070 |
| rs781568147 | snp | C/T | | | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49581667 | CGTAATCTTTGTTGT[C/T]TGTGGGTGGATGTGA | 51070 |
| rs781734698 | snp | A/G | 7.46673e-05 | 0.00610967 | intron-variant | NOSIP | GRCh38.p7 | 19:49556857 | CACCGTGCGTGCCGG[A/G]GCGCTGTGGGGGCTC | 51070 |
| rs796070643 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49563719 | AGGCTGGCCTTGAAC[C/T]CCTGACCTCAGGTGA | 51070 |
| rs796091959 | in-del | -/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49572102 | AGATGCTAAATTTTC[-/T]TTTTTTTTTCTTTTT | 51070 |
| rs796107690 | in-del | -/A | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576146 | TCTTATAAAAAAAAA[-/A]TGTTAAAAACCATTT | 51070 |
| rs796231386 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49569319 | CTGCCTCAGCCTCCT[A/G]AGTAGCTGGGACTAC | 51070 |
| rs796309180 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49569444 | ACCTCGTGATCTGCC[C/T]GCCTCGGCCTTCCAA | 51070 |
| rs796399047 | snp | C/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49555825 | AGCCGGTACCGCCCT[C/G]GGGGAGGTAGAGAGA | 51070 |
| rs796562156 | snp | A/C/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564477 | AAAAAAAAAAAAAAA[A/C/T]AAAATAAAACTTCAT | 51070 |
| rs796688435 | in-del | -/TTTTTT | | | intron-variant | NOSIP | GRCh38.p7 | 19:49558246 | TTCACGTAGCACATC[-/TTTTTT]TTTTTTTTTTTTTTT | 51070 |
| rs796787073 | snp | C/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49559410 | TGGTTCCAGCTACTC[C/G]TGGGGGCTGAGGCAG | 51070 |