SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2379086 | snp | G/T | 0.0333695 | 0.124785 | intron-variant, utr-variant-5-prime | NOSIP | GRCh38.p7 | 19:49574615 | ccagttcctgaggct[G/T]gaagtctaagttcag | 51070 |
rs2379087 | snp | C/T | 0.492582 | 0.0604491 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575019 | AGGCGCCCGCCACCA[C/T]GCCCGGCTAATTTTT | 51070 |
rs3760705 | snp | C/G | 0 | 0 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580720 | CGTGAGTAGCTAATC[C/G]AAAGTTCCGGATATT | 51070 |
rs3760706 | snp | A/C | 0.0908922 | 0.192833 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49581115 | TTAATTTTTCTAGCT[A/C]GGACAGACGAACTCC | 51070 |
rs3760707 | snp | C/T | 0.419936 | 0.183362 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49581197 | CTAATCCCCCAGGTA[C/T]CCCATGGTATTCGAC | 51070 |
rs3760708 | snp | C/G | 0.487746 | 0.0773096 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49581339 | CCACCTGCCAGAAAC[C/G]GGGATCAGGCCTGGT | 51070 |
rs4316869 | snp | C/G | 0.27008 | 0.249192 | intron-variant | NOSIP | GRCh38.p7 | 19:49571900 | tgaggcagaagaatc[C/G]cttgaacccaggagg | 51070 |
rs4426453 | snp | C/T | 0.267636 | 0.249377 | intron-variant | NOSIP | GRCh38.p7 | 19:49559223 | gagactagatttgag[C/T]ttccagctgtcctct | 51070 |
rs4594362 | snp | C/G | 0.203532 | 0.245643 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49556725 | TGACATGGGGCAGGT[C/G]ACCGTGCGGGACTGC | 51070 |
rs5023762 | snp | A/T | 0.415399 | 0.187465 | intron-variant | NOSIP | GRCh38.p7 | 19:49568797 | AAAAAAAAAAAAAAT[A/T]GTTTGTTTGTTTGTT | 51070 |
rs5023763 | snp | G/T | 0.495174 | 0.0488838 | intron-variant | NOSIP | GRCh38.p7 | 19:49568810 | ATAGTTTGTTTGTTT[G/T]TTTTTTTTTTTGAGA | 51070 |
rs5828405 | in-del | -/A | | | intron-variant | NOSIP | GRCh38.p7 | 19:49572985 | TCAAGACTGTGTCTC[-/A]AAAAAAAAAAAAAAA | 51070 |
rs6509437 | snp | A/G | 0.317433 | 0.240734 | intron-variant | NOSIP | GRCh38.p7 | 19:49556461 | GGAGACTCTGATCAG[A/G]GGCCTTCCTGGGGAC | 51070 |
rs6509438 | snp | A/G | 0.254105 | 0.249966 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576194 | caaaaacaggtagcA[A/G]TTACAAAAGTCAGAT | 51070 |
rs7250216 | snp | A/G | 0.242488 | 0.249887 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575912 | caaggcgggcagatc[A/G]tgaggtcaggagatt | 51070 |
rs7254718 | snp | A/G | 0.495855 | 0.045338 | intron-variant | NOSIP | GRCh38.p7 | 19:49569969 | atacaaaaatgagcc[A/G]gtcgtggtggccacc | 51070 |
rs7254831 | snp | C/G | 0.435263 | 0.167862 | intron-variant | NOSIP | GRCh38.p7 | 19:49569980 | agccagtcgtggtgg[C/G]cacctgtaatcccag | 51070 |
rs7255842 | snp | C/T | 0.251014 | 0.249998 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NOSIP, PRRG2 | GRCh38.p7 | 19:49579209 | GTAATGGATAGTAGT[C/T]TAGAATTACGGTTGT | 51070 |
rs7255971 | snp | A/G | 0.251578 | 0.249995 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579373 | AACCAAAATGGAGAC[A/G]CTCATGCTAAAGTTC | 51070 |
rs7257088 | snp | C/T | 0.251014 | 0.249998 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579450 | TCAGGAGAGAGATAA[C/T]AGCCAAATCCCCAAA | 51070 |
rs7258960 | snp | C/T | 0.250168 | 0.25 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578115 | atatgttaggtaaat[C/T]atatcccactaatgc | 51070 |
rs8102979 | snp | A/G | 0.435407 | 0.167703 | intron-variant | NOSIP | GRCh38.p7 | 19:49566637 | AAAGTGGAATAACTG[A/G]TTCAAAGGGTGTGTG | 51070 |
rs8103289 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49566790 | atataaatacatata[C/T]atacatatatatata | 51070 |
rs8103293 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49566794 | aaatacatatacata[C/T]atatatatatataca | 51070 |
rs8103904 | snp | C/T | 0.435407 | 0.167703 | intron-variant | NOSIP | GRCh38.p7 | 19:49566587 | atgaagggtatgagc[C/T]actgcacccaaccCT | 51070 |
rs9304689 | snp | G/T | 0.383439 | 0.21141 | intron-variant | NOSIP | GRCh38.p7 | 19:49571361 | CCTCCAACCAAGGGT[G/T]GAAGAATAGCCAGTT | 51070 |
rs10401626 | snp | A/G | 0.435263 | 0.167862 | intron-variant | NOSIP | GRCh38.p7 | 19:49566490 | attttttatccaggc[A/G]gggtcttgctatgtt | 51070 |
rs10402160 | snp | C/G | 0.118933 | 0.212888 | intron-variant | NOSIP | GRCh38.p7 | 19:49566511 | ttgctatgttgtcca[C/G]gttggtcttgaactc | 51070 |
rs10409856 | snp | C/T | 0.437965 | 0.164831 | intron-variant | NOSIP | GRCh38.p7 | 19:49559783 | CTAGGATCATGCCCA[C/T]GTCCCATGTGAGAAT | 51070 |
rs10410923 | snp | A/G | 0.256897 | 0.249905 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576504 | atcacttgatcccag[A/G]aggttgaggctgcag | 51070 |
rs10412446 | snp | A/G | 0.495891 | 0.0451408 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NOSIP | GRCh38.p7 | 19:49564251 | tgaggtcaggagttc[A/G]agtccagcctggcca | 51070 |
rs10414207 | snp | C/T | 0.121022 | 0.21416 | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49581829 | TCCTTGCTTTCTTCT[C/T]TGGCGGACactgcct | 51070 |
rs10416310 | snp | A/G | 0.495708 | 0.0461266 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576589 | gaccttgtctctggg[A/G]aaaaaaaaaaaaaTg | 51070 |
rs10418031 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | NOSIP | GRCh38.p7 | 19:49570363 | CTCTGGGAGCTATGG[A/C]GCTCTCTCTCCCCCT | 51070 |
rs10418197 | snp | A/G | 0.40086 | 0.199352 | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49578903 | gctgggattacaggc[A/G]tgagccactgtgtct | 51070 |
rs10426466 | snp | C/G | 0.471578 | 0.115772 | intron-variant | NOSIP | GRCh38.p7 | 19:49557428 | CGTTGTATAGCCAGA[C/G]TGCCAGGGCTCAAAG | 51070 |
rs10544127 | in-del | -/AT | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49572676 | TGGAGATACTTTAAA[-/AT]ATATATATATATATG | 51070 |
rs10677626 | in-del | -/TT | | | intron-variant | NOSIP | GRCh38.p7 | 19:49558266 | TTTTTTTTTTTTTTT[-/TT]GAAACAGAATCTCGC | 51070 |
rs11442470 | in-del | -/A | 0.267091 | 0.249415 | intron-variant | NOSIP | GRCh38.p7 | 19:49558210 | GAAACTGAGGCCCAG[-/A]AAAAAATGAGGTGAT | 51070 |
rs11667596 | snp | A/G | 0.00975586 | 0.0691575 | intron-variant | NOSIP | GRCh38.p7 | 19:49573024 | AGACCCTGGCTCTAA[A/G]CATTTTACTGAATAT | 51070 |
rs11879680 | snp | A/G | 0.268724 | 0.249298 | intron-variant | NOSIP | GRCh38.p7 | 19:49561164 | TGGGCACTTAGCTAA[A/G]GCTTGACACTTAGCT | 51070 |
rs11879685 | snp | A/G | 0.268452 | 0.249318 | intron-variant | NOSIP | GRCh38.p7 | 19:49561196 | AGGCTTGACCCAATC[A/G]CTGCCTGCCAGTCCA | 51070 |
rs12610368 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575846 | gtaaaaacgttaaaa[A/C]ccaggccaggcgcag | 51070 |
rs12973615 | snp | A/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49569635 | caacatggtgaaacc[A/C]cgtctctactaaaaa | 51070 |
rs12982495 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NOSIP | GRCh38.p7 | 19:49562224 | cctcccaagttaaag[C/T]gattctcctgcctca | 51070 |
rs12985108 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564476 | aaaaaaaaaaaaaaa[A/C]caaaataaaacttca | 51070 |
rs13346402 | snp | A/G | 0.119281 | 0.213102 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576993 | acctaacacaatttg[A/G]aaatgggtaaaggat | 51070 |
rs17310289 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580364 | AGTGTAGTTCAGCTT[C/G]AAACTTGGGGCGCCC | 51070 |
rs17850728 | snp | A/G | 0 | 0 | missense | NOSIP | GRCh38.p7 | 19:49556909 | GCCTTGGCTTCGGGC[A/G]TCAGCGACGGGATCC | 51070 |
rs34554388 | in-del | -/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564381 | TCGCTTGAACCTGGG[-/T]AGGCGGAGGTTGCAG | 51070 |
rs34789987 | in-del | -/T | | | frameshift-variant | NOSIP | GRCh38.p7 | 19:49556689 | ACGGGCGTCAGGTCC[-/T]GACATGCGCAGGGGC | 51070 |
rs34852716 | in-del | -/A | | | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49578969 | AAAACAGAAGCAGGT[-/A]AAATGAGACCACAAA | 51070 |
rs34899368 | in-del | -/A | 0.5 | 0 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565284 | CTCAAAAAAAAAAAA[-/A]GTCAGGTGCCTTTGG | 51070 |
rs35018027 | in-del | -/A | | | intron-variant | NOSIP | GRCh38.p7 | 19:49561883 | GGCTCTGTCACAATT[-/A]AAAAAAAAAAAAAAA | 51070 |
rs35076085 | in-del | -/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49563496 | TGTGCTTGAAAATTC[-/T]TTTTTTTTTTTTTTG | 51070 |
rs35209614 | in-del | -/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49572407 | TCACTGCACCCAGCC[-/T]TTTTTTTTTTTTTTT | 51070 |
rs35346144 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49574758 | TCACTTTGTCACCTA[A/G]GTTGGAGTGCAGCGG | 51070 |
rs35460081 | in-del | -/A | 0.269267 | 0.249256 | intron-variant | NOSIP | GRCh38.p7 | 19:49559353 | CCTCTCTACAAAAAA[-/A]CAAACAAAAACGCCA | 51070 |
rs35647076 | in-del | -/T | | | frameshift-variant | NOSIP | GRCh38.p7 | 19:49559978 | GAGAGACAACAGCAG[-/T]TCGAAGTCCTTCACG | 51070 |
rs35870721 | in-del | -/AA | | | intron-variant | NOSIP | GRCh38.p7 | 19:49571983 | GTGAGACTCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 51070 |
rs36073675 | in-del | -/G | | | splice-acceptor-variant | NOSIP | GRCh38.p7 | 19:49555824 | AGCCGGTACCGCCCT[-/G]GGGGGAGGTAGAGAG | 51070 |
rs36092424 | in-del | -/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49574732 | CTCCTTCTGTTTTTT[-/G]GGGAGGAGTCTCACT | 51070 |
rs55756060 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49578624 | CAGCCTGGGCAACAT[A/G]GTGACACCTTGTCTC | 51070 |
rs55796141 | snp | A/C | 0.0810805 | 0.184299 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565641 | CACACGCCTGTAATC[A/C]CAGCTACTCAGGAGG | 51070 |
rs56393493 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49578720 | GGCGTGATCTCGGCT[C/T]ACTGCAAGCTCTGCC | 51070 |
rs57705521 | snp | A/G | 0.0123036 | 0.0774623 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579885 | TTTGAACATTTTCGT[A/G]AGAAAACATTAACAT | 51070 |
rs57971225 | in-del | -/CT | | | intron-variant | NOSIP | GRCh38.p7 | 19:49566345 | ACAGGGTCTCACTCT[-/CT]GTCATCTAGGCTGAA | 51070 |
rs58002203 | snp | A/G | 0.266819 | 0.249434 | intron-variant | NOSIP | GRCh38.p7 | 19:49561541 | CCCCCACCCTTTTAA[A/G]TGACTTTATTGAGAC | 51070 |
rs58136999 | in-del | -/A | 0.264084 | 0.249603 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576137 | GAGACTCCATCTTAT[-/A]AAAAAAAAATGTTAA | 51070 |
rs58373948 | in-del | -/TT | | | intron-variant | NOSIP | GRCh38.p7 | 19:49572427 | TTTTTTTTTTTTTTT[-/TT]GAGACAGAGTCTCGC | 51070 |
rs58441193 | in-del | -/AAAA | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576906 | AAAAAAAAAAAAAAA[-/AAAA]TCAGGATATCTGATA | 51070 |
rs58927171 | snp | A/G | 0.27278 | 0.24896 | intron-variant | NOSIP | GRCh38.p7 | 19:49561838 | CAGTGAGCCGACATC[A/G]TGCCACTGCACTCCA | 51070 |
rs58944304 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49562390 | CAGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 51070 |
rs59279440 | snp | C/G/T | 0.299611 | 0.259817 | intron-variant | NOSIP | GRCh38.p7 | 19:49559036 | CCCGCCTCGGCCTCC[C/G/T]GAAGTGCTGGGATTA | 51070 |
rs59474246 | snp | A/G/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49556175 | CAGGAGAAAGCGGGG[A/G/T]GGGGGGGCGGCCTTA | 51070 |
rs59738377 | in-del | -/A | | | intron-variant | NOSIP | GRCh38.p7 | 19:49572993 | AAAAAAAAAAAAAAA[-/A]GCCCGGCTCTGAAGC | 51070 |
rs59880917 | snp | G/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49562389 | TCAGCCTCCCAAAGT[G/T]CTGGGATTACAGGCG | 51070 |
rs59969387 | snp | C/T | 0.0622301 | 0.165053 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564675 | CTATGAGCCAGCAAT[C/T]CGTCTCCCACGTATA | 51070 |
rs60259512 | snp | A/C | 0.00368809 | 0.0427837 | intron-variant | NOSIP | GRCh38.p7 | 19:49556872 | GGCGCTGTGGGGGCT[A/C]ACCGGCTTCTCCAGC | 51070 |
rs60284187 | snp | C/T | 0.17138 | 0.237316 | intron-variant | NOSIP | GRCh38.p7 | 19:49558279 | TTTGAAACAGAATCT[C/T]GCTCGGTTACCCAGG | 51070 |
rs60637720 | in-del | -/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49571156 | TTTTTTTTTTTTTTT[-/T]GTATTTTTTAGTAGA | 51070 |
rs60792250 | snp | A/G | | | intron-variant, utr-variant-5-prime | NOSIP | GRCh38.p7 | 19:49574625 | AGGCTGGAAGTCTAA[A/G]TTCAGGCTACCAGCA | 51070 |
rs61138558 | snp | A/G | 0.17332 | 0.23795 | intron-variant | NOSIP | GRCh38.p7 | 19:49563989 | TAGACAGTCTGCAAG[A/G]TCAAAACTGTTGTCT | 51070 |
rs61302412 | in-del | -/A/AA | 0.49753 | 0.0350569 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577767 | AAAAAAAAAAAAAAA[-/A/AA]GAAGTATTGATACAT | 51070 |
rs62128115 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565000 | GTTATGTGTGGGTGG[G/T]TGTGGTGGCTCACAC | 51070 |
rs62128116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575096 | TCTCTATCTCCTGAC[C/T]TCGTGATCTGCCCAC | 51070 |
rs67179000 | snp | C/T | 0.172674 | 0.237741 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575731 | ACACACAAACGGGCA[C/T]GGCTGTGTTCCAATA | 51070 |
rs67224830 | in-del | -/AGAG | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580305 | GAGAGAGAGAGACAA[-/AGAG]AGAGAGAACTGCCCG | 51070 |
rs67546213 | snp | A/G | 0.263809 | 0.249618 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579330 | TCATTGGTTTGGATT[A/G]AGCTCCTGCACTAGG | 51070 |
rs71180641 | in-del | -/A | 0 | 0 | intron-variant | NOSIP | GRCh38.p7 | 19:49569216 | GCGAGATAACGTCTC[-/A]AAAAAAAAAAAAAAA | 51070 |
rs71294384 | in-del | -/A/G | 0.5 | 0 | intron-variant | NOSIP | GRCh38.p7 | 19:49563510 | GCAAAACTCGATCTC[-/A/G]AAAAAAAAAAAAAAG | 51070 |
rs71294385 | in-del | -/A | 0.5 | 0 | intron-variant | NOSIP | GRCh38.p7 | 19:49563193 | GTGAGTCCCTGTCTC[-/A]AAAAAAAAAAACAAA | 51070 |
rs71735570 | in-del | -/AAAG | | | intron-variant | NOSIP | GRCh38.p7 | 19:49570111 | TCATCTCAAAAAATA[-/AAAG]AAGAAAGAATAAAAT | 51070 |
rs72083126 | in-del | -/TA | | | intron-variant | NOSIP | GRCh38.p7 | 19:49572679 | AGATACTTTAAAATA[-/TA]TATATATATATGGCT | 51070 |
rs72498468 | in-del | -/GAGA | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580312 | AGAGACAAAGAGAGA[-/GAGA]ACTGCCCGATGGACG | 51070 |
rs73057960 | snp | C/T | 0.084728 | 0.187577 | intron-variant | NOSIP | GRCh38.p7 | 19:49561422 | ACAAAACCAGAATAG[C/T]ATAAGGAACCCCCAT | 51070 |
rs73934005 | snp | C/T | 0.268724 | 0.249298 | intron-variant | NOSIP | GRCh38.p7 | 19:49564019 | TTAATAATACTAAGA[C/T]ATTATTTGCCTTTCT | 51070 |
rs73934006 | snp | C/T | 0.264084 | 0.249603 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564949 | ATCCCATTCATGTGA[C/T]GTTCAAAAACTCACA | 51070 |
rs73934007 | snp | C/T | 0.269809 | 0.249214 | intron-variant | NOSIP | GRCh38.p7 | 19:49568440 | TGCTTTGTGTATTCC[C/T]ACACACACACTTATA | 51070 |
rs73934010 | snp | A/T | 0.103438 | 0.202533 | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49579049 | TTAGTTTCTTCAATG[A/T]ATCGATTACACCAAG | 51070 |
rs74182059 | in-del | -/C | 0.5 | 0 | intron-variant | NOSIP | GRCh38.p7 | 19:49567115 | CCACCGTGCCCAGCC[-/C]AAAAAACTTTTTTTT | 51070 |
rs74325716 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | NOSIP | GRCh38.p7 | 19:49558567 | CCCGACCCATTTAGC[A/G]TATCTTTACTAAGGA | 51070 |
rs74491170 | snp | A/G | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49581063 | GGACTAAGGCATATC[A/G]TTCCCGCTAGTTTCT | 51070 |
rs74638421 | snp | G/T | 0.25214 | 0.249991 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577760 | ACAGAGCAAGGCCGT[G/T]TCTCGGGAAAAAAAA | 51070 |
rs74683502 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | NOSIP | GRCh38.p7 | 19:49570205 | GTCTCCTGCTCTCAA[A/G]TAGCCTGCAAGTAGG | 51070 |
rs74861709 | snp | A/G | 0.0901694 | 0.192235 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577955 | GGGGTGGGAAGGATT[A/G]GGAGGAAATAGGGAA | 51070 |
rs74963443 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | NOSIP | GRCh38.p7 | 19:49563903 | CCTAGGCTATAAGAG[G/T]CCAATACTCTTCTAG | 51070 |
rs75150263 | snp | A/C/G | 0.00478085 | 0.0486577 | intron-variant | NOSIP | GRCh38.p7 | 19:49559597 | CCACTAATTGAGCAC[A/C/G]TATTTAGTGCCTGGA | 51070 |
rs75175380 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | NOSIP | GRCh38.p7 | 19:49557794 | CTCAGCCCTGCCTGG[C/T]GCACAGCAGTTGCCT | 51070 |
rs75276320 | snp | A/T | 0.5 | 0 | intron-variant | NOSIP | GRCh38.p7 | 19:49566818 | ATATACACACATACT[A/T]TTTTTTTTTTTTTTT | 51070 |
rs75391587 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564977 | ACAAAGTAATTACTA[C/T]ACCAGAAGTTATGTG | 51070 |
rs75392409 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577143 | TGGAGAAACTGGAAC[A/C]CTTATACATTGGTGG | 51070 |
rs75600346 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565769 | TCTCAAAAGAAAAAA[A/G]AAAGAAAGAAAGAAA | 51070 |
rs75792756 | snp | A/G | 0.250732 | 0.249999 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577625 | AGTAGCTGGCTGGGC[A/G]CCGATGGCTCACACC | 51070 |
rs75917276 | snp | A/G | 0.5 | 0 | intron-variant | NOSIP | GRCh38.p7 | 19:49561901 | AAAAAAAAAAAAAAA[A/G]ACATTGCCTAAGCCA | 51070 |
rs76104237 | snp | A/C | 0 | 0 | intron-variant | NOSIP | GRCh38.p7 | 19:49571983 | AGTGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 51070 |
rs76138951 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49578938 | TATTTTTAAATACTT[A/C]AAAAAAAAAAGAAAG | 51070 |
rs76329048 | snp | A/T | 0.5 | 0 | intron-variant | NOSIP | GRCh38.p7 | 19:49568795 | AAAAAAAAAAAAAAA[A/T]TAGTTTGTTTGTTTG | 51070 |
rs76387200 | snp | C/T | 0.0501905 | 0.150254 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580957 | TACGCTCCCATTTTA[C/T]AGACAGAGCCATTGG | 51070 |
rs76392215 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | NOSIP | GRCh38.p7 | 19:49570522 | ACAGAACCTTCCTAT[A/C]ACGCTAAATACCCCC | 51070 |
rs76452014 | snp | A/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49573788 | TGCCCATTTATTTTA[A/T]TTTATGTATGTATGT | 51070 |
rs76713826 | snp | G/T | 0.5 | 0 | intron-variant | NOSIP | GRCh38.p7 | 19:49568822 | TTTGTTTTTTTTTTT[G/T]AGACAGAGTCTTGCT | 51070 |
rs76791046 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578141 | AATGCTTTTTTTTTT[G/T]GAGAGGGAGTTATGC | 51070 |
rs76892655 | snp | A/T | 0.5 | 0 | intron-variant | NOSIP | GRCh38.p7 | 19:49573857 | CACCAGGACTGAAGT[A/T]TTTTTTTTTTTTTTT | 51070 |
rs77035369 | snp | G/T | 0.5 | 0 | intron-variant | NOSIP | GRCh38.p7 | 19:49573878 | TTTTTTTTTTTTTTG[G/T]AGACGGAGTCTCACT | 51070 |
rs77080188 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | NOSIP | GRCh38.p7 | 19:49568487 | TGGATTCACCTTGGA[C/T]GCACATAAGCAAATG | 51070 |
rs77104982 | snp | C/T | 0.046775 | 0.145601 | intron-variant | NOSIP | GRCh38.p7 | 19:49564078 | AGGCTCCATGAGGTG[C/T]GACACTGCAACACTA | 51070 |
rs77124124 | snp | C/T | 0.0644693 | 0.167566 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577148 | AAACTGGAACCCTTA[C/T]ACATTGGTGGTAGAA | 51070 |
rs77164262 | snp | C/T | 0.00557542 | 0.0525036 | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555080 | GCAGCCCGGAAGACA[C/T]GTTCCTGGGCATTTC | 51070 |
rs77192141 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | NOSIP | GRCh38.p7 | 19:49561195 | AAGGCTTGACCCAAT[C/T]GCTGCCTGCCAGTCC | 51070 |
rs77591237 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | NOSIP | GRCh38.p7 | 19:49573210 | GACCATCCACTGTGC[C/T]AGCTGGCTGCAGGCG | 51070 |
rs77632193 | snp | C/T | 0.0134861 | 0.0810011 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579817 | TGGCAAAAATAATCA[C/T]TGGTGATTTGGGTGA | 51070 |
rs77834683 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | NOSIP | GRCh38.p7 | 19:49560358 | TTGGGCCTCAGTTTC[C/T]TCCTCTGGAACATGG | 51070 |
rs77958165 | snp | C/T | 0.5 | 0 | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555269 | GTTTTTTTTTTTTTT[C/T]CTTCTTTGAGATGGA | 51070 |
rs78063993 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | NOSIP | GRCh38.p7 | 19:49573204 | GGCTTTGACCATCCA[C/T]TGTGCCAGCTGGCTG | 51070 |
rs78161006 | snp | G/T | 0.5 | 0 | intron-variant | NOSIP | GRCh38.p7 | 19:49568821 | GTTTGTTTTTTTTTT[G/T]GAGACAGAGTCTTGC | 51070 |
rs78535027 | snp | A/T | 0.268724 | 0.249298 | intron-variant | NOSIP | GRCh38.p7 | 19:49562923 | GTAACATTATATACT[A/T]GTCTCACTCATCTCT | 51070 |
rs78655382 | snp | A/T | 0.5 | 0 | intron-variant | NOSIP | GRCh38.p7 | 19:49568796 | AAAAAAAAAAAAAAA[A/T]AGTTTGTTTGTTTGT | 51070 |
rs78936857 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576949 | CAGTGAGAATATATT[A/T]AAAACTTACAACTCA | 51070 |
rs79151664 | snp | C/T | 0.0422918 | 0.139132 | intron-variant | NOSIP | GRCh38.p7 | 19:49559023 | AGAAAGTGATCCTCC[C/T]GCCTCGGCCTCCCGA | 51070 |
rs79563605 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576331 | AACCCTGTCTCTACC[A/C]AAAAAAAGCAGCAGC | 51070 |
rs79657469 | snp | C/T | 0.0460142 | 0.144533 | upstream-variant-2KB, utr-variant-5-prime | PRRG2, NOSIP | GRCh38.p7 | 19:49580699 | TTCTCTTTCTCTCTC[C/T]GGAAACGTGAGTAGC | 51070 |
rs79796602 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565969 | GTACCCAATGTCTAG[C/T]ACGTGTCCAAGGATG | 51070 |
rs79903573 | snp | A/G | 0.269267 | 0.249256 | intron-variant | NOSIP | GRCh38.p7 | 19:49556010 | AGGGCGCAGAGAAGA[A/G]GGTAGAGAGTGGCAG | 51070 |
rs80099527 | snp | A/C | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577221 | AAAAGGTTAAATAGT[A/C]ACCTTTTGACCCAGC | 51070 |
rs80132158 | snp | G/T | 0 | 0 | intron-variant | NOSIP | GRCh38.p7 | 19:49573876 | TTTTTTTTTTTTTTT[G/T]GGAGACGGAGTCTCA | 51070 |
rs80273146 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NOSIP | GRCh38.p7 | 19:49571500 | CAGCATTTCAGAGAG[A/G]AAACAGGCAAAGAGC | 51070 |
rs80316078 | snp | A/T | 0 | 0 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576910 | AAAAAAAAAAAAAAA[A/T]CAGGATATCTGATAA | 51070 |
rs111261691 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | NOSIP | GRCh38.p7 | 19:49566316 | TGAGCCACTGCGCCC[A/G]GCCTTTTCTTTAAGA | 51070 |
rs111299973 | snp | C/T | 0.0133292 | 0.0805416 | intron-variant | NOSIP | GRCh38.p7 | 19:49558867 | AAAAGCTCCTGCCTC[C/T]GTGTGCCGCCTCCTC | 51070 |
rs111310942 | in-del | -/AAAG | 0.495927 | 0.0449436 | intron-variant | NOSIP | GRCh38.p7 | 19:49570110 | CTCATCTCAAAAAAT[-/AAAG]AAAGAAAGAATAAAA | 51070 |
rs111347791 | snp | A/T | 0.5 | 0 | intron-variant | NOSIP | GRCh38.p7 | 19:49572601 | TATTTTTATATTTGT[A/T]TTTTTAGCACAGATG | 51070 |
rs111381088 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49578829 | GGGGTTTCACCGTGT[C/T]AGCCAGGATGGTCTT | 51070 |
rs111412602 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | NOSIP | GRCh38.p7 | 19:49561943 | ATTTATTCCTATGTT[C/T]TCTTCTAGGGGTTTG | 51070 |
rs111502023 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576562 | TGCACTCCAGACTGA[A/G]TGACAGAGTGAGACC | 51070 |
rs111522016 | snp | A/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49557040 | CCCCTGGGCCCGCCC[A/C]GCCCGCGGCGCCCCG | 51070 |
rs111544701 | snp | C/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580252 | TAACTCTCAGGAGAA[C/G]TGGCCGATGCTAGCT | 51070 |
rs111549729 | in-del | -/TTC | 0.5 | 0 | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555265 | CAGGTTTTTTTTTTT[-/TTC]TTTTCTTCTTTGAGA | 51070 |
rs111764736 | snp | C/G | 0 | 0 | splice-donor-variant | NOSIP | GRCh38.p7 | 19:49560621 | CACCCCAGCCCTGCA[C/G]CTGTGTCCTTCTTCT | 51070 |
rs111899615 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NOSIP | GRCh38.p7 | 19:49555928 | AAGGTGAAGCGGGTT[G/T]CTGGCTAAGGAGTAG | 51070 |
rs111914751 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSIP | GRCh38.p7 | 19:49569002 | GAGATGGGCTTTCAC[C/T]ACGTTGGTCACGATG | 51070 |
rs111915322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49560132 | GCACAGAGACAACGC[A/G]GTGGTGGGGGTGGGG | 51070 |
rs111964820 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49581258 | TAAGTCCTTTATCCC[A/C]AGGTCCCTTTAAATA | 51070 |
rs111967252 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | NOSIP | GRCh38.p7 | 19:49567936 | GGCCACCTTGGCTTC[C/T]CAAAGTGCTGGGATT | 51070 |
rs112071722 | snp | A/G | 0.5 | 0 | intron-variant | NOSIP | GRCh38.p7 | 19:49556052 | TGGGAGGGAGCGTGT[A/G]GAGGGGGTGGAGCCG | 51070 |
rs112120564 | snp | G/T | 0.272511 | 0.248984 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555652 | CTGTTTGCACGGCCC[G/T]GCATCCTCGCCTGCC | 51070 |
rs112203383 | snp | G/T | 0.5 | 0 | intron-variant | NOSIP | GRCh38.p7 | 19:49570110 | ACTCATCTCAAAAAA[G/T]AAAGAAAGAATAAAA | 51070 |
rs112278233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49568381 | TGGCTCCTAACACCC[A/G]GGGAACTGCGGTGGT | 51070 |
rs112364244 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | NOSIP | GRCh38.p7 | 19:49558417 | TGCCCGGCTCAATTT[A/T]TTTTTTTATTTTTTT | 51070 |
rs112390792 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | NOSIP | GRCh38.p7 | 19:49567097 | CTGGGATTATAGGCA[C/G/T]GAGCCACCGTGCCCA | 51070 |
rs112494970 | in-del | -/A | 0.5 | 0 | intron-variant | NOSIP | GRCh38.p7 | 19:49559511 | TGAAGACTCTGTCTC[-/A]AAAAAAAAAAAAGAA | 51070 |
rs112559857 | snp | C/T | 0.268724 | 0.249298 | intron-variant | NOSIP | GRCh38.p7 | 19:49562242 | TTCTCCTGCCTCAGC[C/T]TCCCAAATAGCAGGG | 51070 |
rs112673105 | snp | A/G | 0.153 | 0.230415 | intron-variant | NOSIP | GRCh38.p7 | 19:49569018 | ACGTTGGTCACGATG[A/G]TCTCGAACTCCTGAC | 51070 |
rs112795659 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NOSIP | GRCh38.p7 | 19:49557526 | TAAAACAGCCTAACA[A/G]TGGTTACCCACCTCA | 51070 |
rs112845138 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576936 | GATAAGGGAATTGCA[C/G]TGAGAATATATTAAA | 51070 |
rs112911651 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49574839 | TAGCTGGGATTACAG[A/G]CGTCCACCACCATGC | 51070 |
rs112971713 | snp | C/G | 0.267636 | 0.249377 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49566155 | CTCCCGAGTAGCTGG[C/G]ACTACAGGCGCTCGC | 51070 |
rs113004387 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49560430 | GAGTTCATGCGCAGA[A/C]GGCAGAGAACACAGT | 51070 |
rs113017910 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580219 | ACCAGCAAATAGCCA[A/T]CATCTACAGCAGAAC | 51070 |
rs113086320 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NOSIP | GRCh38.p7 | 19:49562793 | GGCTGAAACAGGAGA[C/T]TCATTGAACCTGGGA | 51070 |
rs113205442 | snp | A/G | 0.437824 | 0.164991 | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49582170 | CGCTTGAACCCAGGA[A/G]GCAGAGGTCACAGTG | 51070 |
rs113221080 | snp | G/T | | | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49581575 | GTTTGGGGCTCCTAG[G/T]CCCAGGAGTCCAGGG | 51070 |
rs113238098 | snp | A/C/G | 1.88848e-05 | 0.00307279 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49560035 | GGTCCCATAGCCCGA[A/C/G]GCCGCTGGGGACAGA | 51070 |
rs113342714 | snp | A/G | 0.00557542 | 0.0525036 | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555464 | AGGTTTCACCATGTT[A/G]GCCAGGCTGGTCTCG | 51070 |
rs113359421 | snp | A/T | 0.5 | 0 | intron-variant | NOSIP | GRCh38.p7 | 19:49570106 | AGACACTCATCTCAA[A/T]AAATAAAGAAAGAAT | 51070 |
rs113413023 | snp | C/T | 0.242201 | 0.249878 | intron-variant | NOSIP | GRCh38.p7 | 19:49566808 | ACATATATATATATA[C/T]ACACATACTATTTTT | 51070 |
rs113485844 | in-del | -/T | 0.5 | 0 | intron-variant | NOSIP | GRCh38.p7 | 19:49563497 | TGTGCTTGAAAATTC[-/T]TTTTTTTTTTTTTGA | 51070 |
rs113616249 | snp | A/T | 0.172351 | 0.237636 | intron-variant | NOSIP | GRCh38.p7 | 19:49569746 | CCGGGAGGTGGAGGT[A/T]GCAGTGAGCCAAGAT | 51070 |
rs113646831 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NOSIP | GRCh38.p7 | 19:49557449 | GGGCTCAAAGCCCAT[C/T]TCTGTCACTCTGTGG | 51070 |
rs113671571 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576580 | ACAGAGTGAGACCTT[A/G]TCTCTGGGGAAAAAA | 51070 |
rs113710641 | snp | A/G | 0.172351 | 0.237636 | intron-variant | NOSIP | GRCh38.p7 | 19:49569582 | GAGGCCGAGGTGGGC[A/G]GATCACTTGAGGTCA | 51070 |
rs113717609 | snp | C/T | 0.5 | 0 | intron-variant | NOSIP | GRCh38.p7 | 19:49560177 | CAGGCAGTTGGGAGC[C/T]GCTGCCTGTGTGCTG | 51070 |
rs113772423 | in-del | -/AAAGG/AAGG | 0.164368 | 0.245579 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565770 | TCAAAAGAAAAAAAA[-/AAAGG/AAGG]AAGAAAGAAAGAAAG | 51070 |
rs113801859 | snp | C/T | 0.000401274 | 0.0141589 | intron-variant | NOSIP | GRCh38.p7 | 19:49555857 | GGACGAGGTAGAGGC[C/T]GGCCCGGGGGTGACC | 51070 |
rs113980263 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NOSIP | GRCh38.p7 | 19:49567599 | TGCTGTGGAAAATGT[A/G]CCATCAGTGAGAGAC | 51070 |
rs114181391 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | NOSIP | GRCh38.p7 | 19:49560423 | GAGGAGTGAGTTCAT[G/T]CGCAGAAGGCAGAGA | 51070 |
rs114223209 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | NOSIP | GRCh38.p7 | 19:49555923 | GGGTCAAGGTGAAGC[C/G]GGTTGCTGGCTAAGG | 51070 |
rs114470680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49574019 | CACACACCACCATGC[C/T]TAGATACTTTTTTTG | 51070 |
rs114505227 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565465 | TGTTATAAAAAGAAA[C/T]TGGCTGGGTGCCATG | 51070 |
rs114815845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49560144 | CGCGGTGGTGGGGGT[A/G]GGGGACTCAGAGAGA | 51070 |
rs114856668 | snp | C/G | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579654 | TATTTTCCATAATTA[C/G]ATGTTGTTTGATTGT | 51070 |
rs114999509 | snp | C/T | 0.0513262 | 0.151752 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564848 | AATGAGACACAACAG[C/T]CTACTGTCATACCCA | 51070 |
rs115161823 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | NOSIP | GRCh38.p7 | 19:49567423 | ACCGTGCCCGGCCCC[A/C]AAAATTTTTTTGTTA | 51070 |
rs115172993 | snp | A/G | 0.27008 | 0.249192 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565762 | GAACCTGTCTCAAAA[A/G]AAAAAAAAAAGAAAG | 51070 |
rs115716398 | snp | G/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580829 | CAGGTTTTGAGTCTC[G/T]CCAAGCCCAAATTTA | 51070 |
rs115929576 | snp | A/G | 0.0748431 | 0.178382 | intron-variant | NOSIP | GRCh38.p7 | 19:49561775 | TAATCCCAACTACTC[A/G]GGAGGCTGAGGCACT | 51070 |
rs117317756 | snp | A/G | 0.118933 | 0.212888 | intron-variant | NOSIP | GRCh38.p7 | 19:49562658 | AGCCGAGGCGGGGGC[A/G]GATCACGAGATCAAG | 51070 |
rs117515856 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NOSIP | GRCh38.p7 | 19:49557589 | TTTACAGCATGGAGA[C/G]CCTCACCTGGCACTC | 51070 |
rs117679843 | snp | C/T | 0.0209421 | 0.100162 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564911 | GCGAGACACCAGACA[C/T]GCAAAAGAAAACTTA | 51070 |
rs117807116 | snp | C/T | 0.0126979 | 0.078662 | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555173 | AGCTCATTAAAGTGG[C/T]GCACTCACACGGTCT | 51070 |
rs118134875 | snp | A/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49570744 | TCCCCAGCCCCCACA[A/C]CTGCCACTCATGAAG | 51070 |
rs137962315 | snp | C/G | 0.0490535 | 0.14873 | intron-variant | NOSIP | GRCh38.p7 | 19:49571224 | CTCCTGATCTCAAGT[C/G]ATCCGCCCACCTCAG | 51070 |
rs138001141 | snp | A/G | 2.65968e-05 | 0.0036466 | missense | NOSIP | GRCh38.p7 | 19:49557180 | GGAAGCCCCGCACAT[A/G]GTCCTGCGAGGCCGC | 51070 |
rs138047585 | snp | A/C/T | 0.000557134 | 0.016681 | intron-variant | NOSIP | GRCh38.p7 | 19:49557253 | CTTCTCGTAGGCCTG[A/C/T]GTCGGGGAAAGTGGG | 51070 |
rs138157240 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSIP | GRCh38.p7 | 19:49563272 | CCTTGACCTCCTGGG[C/T]TCAAGTGATTCTCCT | 51070 |
rs138256115 | snp | A/G | 5.2515e-05 | 0.00512394 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49559993 | GTCGAAGTCCTTCAC[A/G]GCATCCCGGCTCAGT | 51070 |
rs138525847 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | NOSIP | GRCh38.p7 | 19:49576745 | CAAAATTAGCTGGGC[A/G]TGGTGGTGCATACCT | 51070 |
rs138559475 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579915 | TCAAACTGCCTCAAG[C/G]ACCGTTCAAGCCCCA | 51070 |
rs138800920 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NOSIP | GRCh38.p7 | 19:49557898 | CTCATGAGGGCCTCC[A/G]ACATGACCACCAGGC | 51070 |
rs138827072 | in-del | -/G | 0.190519 | 0.242821 | intron-variant | NOSIP | GRCh38.p7 | 19:49560513 | CCATCAGTGTATATC[-/G]GGGGGCGGGAGAGAG | 51070 |
rs139174033 | snp | C/T | 0.0368353 | 0.130617 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577417 | CAAAAATTAGCTAGG[C/T]GTGGTAGCGCATGCC | 51070 |
rs139242177 | snp | C/G | 0.046775 | 0.145601 | intron-variant | NOSIP | GRCh38.p7 | 19:49563607 | CAAGCAATTCTCCTG[C/G]CTCAGCCTCCTAAGT | 51070 |
rs139308491 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49566210 | ATTTTTTAGTGAAAA[C/T]GGGGTTTCACCGTGT | 51070 |
rs139530582 | snp | C/T | 0.00835141 | 0.0640778 | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555082 | AGCCCGGAAGACACG[C/T]TCCTGGGCATTTCCT | 51070 |
rs139745113 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49573746 | CATGTGAACACATTC[A/G]GTCCTCATGACAACC | 51070 |
rs139830739 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | NOSIP | GRCh38.p7 | 19:49571885 | AGCTGCTCGGGAGGC[C/T]GAGGCAGAAGAATCG | 51070 |
rs140256795 | in-del | -/AGAC | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564531 | ACAAGGGTTGCAATT[-/AGAC]AGAGGGGTGCAGGCG | 51070 |
rs140289673 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580091 | TGCACAATCTAGTAT[C/T]GCCCGCCGTCCCACC | 51070 |
rs140289937 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NOSIP | GRCh38.p7 | 19:49559074 | AAGTCATCATGATCA[A/G]TCCCAAGTTCAATTA | 51070 |
rs140329218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49568579 | ATTTTCAAAATAAGC[A/G]TTATAGCAGAACTGA | 51070 |
rs140348821 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564625 | ACTTTGGAAAGCAAC[C/T]GTCAGTATCTACTGA | 51070 |
rs140544290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577992 | CTAATGAGTACCAGG[A/G]TTTCTTTTTGGGTGA | 51070 |
rs140688649 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NOSIP, PRRG2 | GRCh38.p7 | 19:49579172 | CAAACCCACAGTTAC[A/C]CTGGACTTGACTCTG | 51070 |
rs140793974 | snp | A/G | 0.00111898 | 0.023627 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49557220 | CTCCTTCTGCTCCTC[A/G]CGCCGGGTGCCCCGC | 51070 |
rs140956669 | snp | A/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49558578 | TAGCATATCTTTACT[A/T]AGGACCTAAGCTACA | 51070 |
rs141037707 | snp | A/G | 0.27278 | 0.24896 | intron-variant | NOSIP | GRCh38.p7 | 19:49561680 | TGAGTTCAGGAGTTC[A/G]AGATCAGCCTGGCCA | 51070 |
rs141077974 | snp | A/G | 0.000375223 | 0.013692 | missense | NOSIP | GRCh38.p7 | 19:49556714 | AGGGGCTTCCCTGAC[A/G]TGGGGCAGGTCACCG | 51070 |
rs141572954 | snp | C/T | 0.0901694 | 0.192235 | intron-variant, utr-variant-5-prime | NOSIP | GRCh38.p7 | 19:49576846 | CCAAGATCGCACCAT[C/T]GCACTCCAGCCTAGG | 51070 |
rs141576321 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSIP | GRCh38.p7 | 19:49574452 | CTGATGGGGCCTGGA[C/T]AGTCACAGGATGCTA | 51070 |
rs141824166 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSIP | GRCh38.p7 | 19:49570277 | GATGTAAAAAGCAAC[C/T]TCATCTCTATCGCCC | 51070 |
rs141972101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49570726 | CCCTCACCTGCCATC[C/T]GCTCCCCAGCCCCCA | 51070 |
rs142124376 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564663 | CATATGCCAGTCCTA[G/T]GAGCCAGCAATTCGT | 51070 |
rs142202252 | snp | C/G | 6.79521e-05 | 0.0058285 | missense | NOSIP | GRCh38.p7 | 19:49556395 | CTTCCGAATCAGCTT[C/G]TCCACGCATTCGAGG | 51070 |
rs142459483 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOSIP | GRCh38.p7 | 19:49571429 | CCCACACTATATTGT[C/T]TCTTTGGTAGGTCCA | 51070 |
rs142712662 | in-del | -/CA | 0.0271762 | 0.113356 | intron-variant | NOSIP | GRCh38.p7 | 19:49568440 | TGCTTTGTGTATTCC[-/CA]CACACACACTTATAG | 51070 |
rs142755455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578582 | AGGCCAAGGCAGGAG[A/G]ATCGCTTAAGCCCAG | 51070 |
rs142865904 | in-del | -/TATGTATG | | | intron-variant | NOSIP | GRCh38.p7 | 19:49573791 | CCATTTATTTTATTT[-/TATGTATG]TATGTATGTATGTAT | 51070 |
rs143185235 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555625 | CAAACTCCAGCGTGC[A/G]CTGTAGGAGCACTGT | 51070 |
rs143317407 | snp | C/T | 0.239037 | 0.24976 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575118 | TCTGCCCACCTCGGC[C/T]TCCCAAAGTGCTGGG | 51070 |
rs143322951 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NOSIP | GRCh38.p7 | 19:49566302 | TGGGATTACAGGCGT[A/G]AGCCACTGCGCCCGG | 51070 |
rs143333070 | snp | A/C | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565796 | GAAAGAAATTAATGG[A/C]GGGGGAACCCCCACT | 51070 |
rs143429751 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49581615 | ACTTAGGTCCCTAGA[C/T]CCAATAATATAACTA | 51070 |
rs143501055 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | NOSIP | GRCh38.p7 | 19:49568092 | CTTACAGAGAAAACA[A/G]GATTGTGTCACAATC | 51070 |
rs144005571 | snp | A/C | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577932 | CAGAGTAGTGGCTGC[A/C]AAAGACTGGGGTGGG | 51070 |
rs144010181 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NOSIP | GRCh38.p7 | 19:49567748 | GATCTCGGCTCACTG[A/C]AACCTCTCTGCCTCC | 51070 |
rs144210466 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | NOSIP | GRCh38.p7 | 19:49562678 | ACGAGATCAAGAGAT[C/T]GAGACCATCCTGGCC | 51070 |
rs144456712 | in-del | -/T | | | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555254 | TGCGTTCTATTCAGG[-/T]TTTTTTTTTTTTTTT | 51070 |
rs144509743 | snp | C/T | 0.107341 | 0.205301 | intron-variant | NOSIP | GRCh38.p7 | 19:49566962 | CTGGGATTACAGGCG[C/T]GCACCACCATGCCCA | 51070 |
rs144663719 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NOSIP, PRRG2 | GRCh38.p7 | 19:49579285 | TCTGGTTTTTACACA[C/T]GCACCCTGTTAGATA | 51070 |
rs144701378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578180 | CCAGGCTGGAGTGAA[A/G]TGGCATGATCTCAGC | 51070 |
rs144739901 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | NOSIP | GRCh38.p7 | 19:49573814 | TATGTATGTATGTAT[G/T]TATTTATTTTGGAGA | 51070 |
rs144834585 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NOSIP | GRCh38.p7 | 19:49558154 | CTCCCAGGTGCCCTG[C/T]TGTGTCCTCTGATTT | 51070 |
rs145052569 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49562240 | GATTCTCCTGCCTCA[G/T]CTTCCCAAATAGCAG | 51070 |
rs145072172 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOSIP | GRCh38.p7 | 19:49557737 | CCCATGTCTATGGAC[A/G]GACAGTGAGTGAGGA | 51070 |
rs145166031 | snp | A/G | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580308 | AGAGAGAGACAAAGA[A/G]AGAGAGAACTGCCCG | 51070 |
rs145430655 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49574921 | AGGCTGGAGTGCAGT[A/G]GCGTGATCTCGGCTC | 51070 |
rs145461288 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NOSIP | GRCh38.p7 | 19:49559553 | CCTTGGGGGCCCTGA[C/T]CATTAATTACTGTCT | 51070 |
rs145685401 | in-del | -/G | 0.0475351 | 0.146656 | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49581574 | AGTTTGGGGCTCCTA[-/G]GCCCAGGAGTCCAGG | 51070 |
rs145801748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49579099 | GAAGGGGGAACAGTT[C/T]TAAATTAAGAGAGAT | 51070 |
rs145929707 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NOSIP | GRCh38.p7 | 19:49571637 | AGGCTCTGGAGCCAT[A/T]CCTTTTAACTAGGTG | 51070 |
rs146278155 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | NOSIP | GRCh38.p7 | 19:49569709 | GCTACTCAGGAGGCT[A/G]AGGCAAGAGAATTGC | 51070 |
rs146481382 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NOSIP | GRCh38.p7 | 19:49561289 | AGTAGGGCTCTGTGT[C/T]TAGGGGAAGAGCTAC | 51070 |
rs146506884 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49574082 | GGCCAGGCTGGGTCT[C/T]GAACTCCTGACCTCA | 51070 |
rs146521136 | snp | A/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49570741 | CGCTCCCCAGCCCCC[A/C]CAACTGCCACTCATG | 51070 |
rs146531011 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565487 | GGTGCCATGGTGCAC[A/G]CCTGTAATCTCAGCA | 51070 |
rs146638349 | in-del | -/T | 0.159292 | 0.232964 | intron-variant | NOSIP | GRCh38.p7 | 19:49558413 | CCATGCCCGGCTCAA[-/T]TTTTTTTTTTTATTT | 51070 |
rs146732618 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565894 | ATCCCTGAATGAACA[C/G]AACTCTTGGATTTGA | 51070 |
rs147065466 | snp | A/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49570743 | CTCCCCAGCCCCCAC[A/C]ACTGCCACTCATGAA | 51070 |
rs147179302 | in-del | -/AAAG/AAAGAAAGAAAG | 0.271694 | 0.251751 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565769 | CTCAAAAGAAAAAAA[-/AAAG/AAAGAAAGAAAG]AAAGAAAGAAAGAAA | 51070 |
rs147333823 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NOSIP | GRCh38.p7 | 19:49563579 | GCTCACTACAACCTC[C/T]GCCTCTTGGGTTCAA | 51070 |
rs147513478 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564410 | AGTGAGCCAAGATCA[C/T]GCCACGGCACTCTAG | 51070 |
rs147558794 | snp | A/C | 0.0279526 | 0.114869 | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555344 | GCTCACTGCAACCTC[A/C]GCCTCCTGGGTTCAA | 51070 |
rs147601481 | snp | A/G | 0.000955739 | 0.0218393 | intron-variant | NOSIP | GRCh38.p7 | 19:49558868 | AAAGCTCCTGCCTCC[A/G]TGTGCCGCCTCCTCC | 51070 |
rs147738108 | in-del | -/ATAT | | | intron-variant | NOSIP | GRCh38.p7 | 19:49566794 | AATACATATACATAC[-/ATAT]ATATATATATATACA | 51070 |
rs147853428 | snp | A/G | 0.00205248 | 0.03197 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49556602 | GCTGTCGCGGGTCAC[A/G]GCACACACGTAGCGC | 51070 |
rs147873215 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NOSIP | GRCh38.p7 | 19:49574202 | TGAAGCTTGGAGAAA[C/T]TGGCCTCTTCCTCAG | 51070 |
rs147916365 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578257 | GCCTCCTGAGTAGCT[C/G]GGATTATAGGTGCCA | 51070 |
rs147984831 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49581808 | AAAGAAAGATAAGCT[C/G]CCTGCTCCTTGCTTT | 51070 |
rs148081494 | snp | G/T | 0.266819 | 0.249434 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49566059 | CAGTCTCGCTCTGTC[G/T]TCCAGGCTGGAGTGC | 51070 |
rs148134920 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49570621 | CAAACACCCCAACTT[C/G]ACCCAGGGTCCCCTC | 51070 |
rs148356584 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575508 | CCCAGGCAGTATGCA[A/C]CATGAAGCGACCAGC | 51070 |
rs148452499 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOSIP | GRCh38.p7 | 19:49572558 | ACTGGAATTCCAGGC[A/G]TGTGCCACCATGCCC | 51070 |
rs148573881 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NOSIP | GRCh38.p7 | 19:49558306 | CAGGCTGAAGTGCAG[C/T]GGTGCCATCTCAGCT | 51070 |
rs148894998 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49559568 | TCATTAATTACTGTC[G/T]TCTACAAAATATACC | 51070 |
rs148946256 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565926 | ACCTGTGGACAGACA[A/T]CCTTGTCCACTATGA | 51070 |
rs149091874 | snp | C/G/T | 6.76594e-05 | 0.00581599 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49555805 | CTTCACTCCGGAGCC[C/G/T]GCGAAGCCGGTACCG | 51070 |
rs149266629 | snp | C/T | 0.26326 | 0.249648 | intron-variant | NOSIP | GRCh38.p7 | 19:49566960 | AGCTGGGATTACAGG[C/T]GCGCACCACCATGCC | 51070 |
rs149362918 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NOSIP | GRCh38.p7 | 19:49557927 | GCTGTGTGGAGGACA[C/T]GGGCACAGGGGGAGC | 51070 |
rs149541537 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577627 | TAGCTGGCTGGGCGC[C/T]GATGGCTCACACCTG | 51070 |
rs149618546 | snp | A/C | 0.00114188 | 0.023867 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49560038 | CCCATAGCCCGAGGC[A/C]GCTGGGGACAGAGAT | 51070 |
rs149636671 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NOSIP | GRCh38.p7 | 19:49563333 | GGCATGTGCCACCAC[A/G]CCCAGCTAATTTTTA | 51070 |
rs149656652 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NOSIP | GRCh38.p7 | 19:49559394 | TGGTAGTGCACACCC[A/G]TGGTTCCAGCTACTC | 51070 |
rs149951413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565302 | CAGGTGCCTTTGGGA[A/G]GCAGAAGGTGGGGGT | 51070 |
rs150009238 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NOSIP | GRCh38.p7 | 19:49568680 | CTGGGTGCCGTGGCT[C/T]ATGCCTGTAATCCCA | 51070 |
rs150046263 | snp | A/C/G | 0.00716625 | 0.0594738 | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555019 | TAGTCCGGGTGCTGC[A/C/G]CACTTTTTCACAGAA | 51070 |
rs150321437 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NOSIP | GRCh38.p7 | 19:49570975 | CATTTAAACTTTTTT[A/T]AATTTAATTTGTTTT | 51070 |
rs150449733 | snp | C/T | 4.36929e-05 | 0.00467382 | splice-donor-variant | NOSIP | GRCh38.p7 | 19:49559933 | CCTGTTCCCAGCTCA[C/T]GTGACAACAGGATCG | 51070 |
rs150597059 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49581889 | CACTGTGTGACCTTC[A/G]GCAAGCTATATTACC | 51070 |
rs150658505 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NOSIP | GRCh38.p7 | 19:49558554 | GTGAGCCACCACCCC[C/T]GACCCATTTAGCATA | 51070 |
rs150709250 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564718 | GGGTACACCTGTTTA[C/T]AAGACACATACACTG | 51070 |
rs150720822 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577287 | ATGCAGGCGGGGCGC[A/G]GTGGCTCATGCCTGT | 51070 |
rs150983984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49573407 | GCCCTGAGCTACCTC[C/T]GTTACAGCCCGTCCC | 51070 |
rs151017072 | snp | C/G/T | 0.000416514 | 0.0144258 | NOSIP | 19 | allele_origin=T(somatic)/C(germline) | 19:49557219 | GCTCCTTCTGCTCCT[C/G/T]GCGCCGGGTGCCCCG | 51070 |
rs151037512 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49578621 | GACCAGCCTGGGCAA[C/T]ATAGTGACACCTTGT | 51070 |
rs151233389 | snp | C/G/T | 0.00030027 | 0.0122495 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49555766 | TCAGGCCTGCATCAC[C/G/T]GGCCGTGATTTCTCC | 51070 |
rs151278421 | snp | C/G | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580306 | AGAGAGAGAGACAAA[C/G]AGAGAGAGAACTGCC | 51070 |
rs180915534 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | NOSIP | GRCh38.p7 | 19:49571174 | ATTTTTTAGTAGAGA[C/G]AGGGTTTCACCATGT | 51070 |
rs181192547 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49562385 | TGCCTCAGCCTCCCA[A/T]AGTGCTGGGATTACA | 51070 |
rs181315057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49570185 | AGTTGCATTCAGGAA[A/G]GATTGTCTCCTGCTC | 51070 |
rs181358097 | snp | A/C/G | 0.00551284 | 0.0522179 | intron-variant | NOSIP | GRCh38.p7 | 19:49555826 | GCCGGTACCGCCCTG[A/C/G]GGGAGGTAGAGAGAA | 51070 |
rs181401946 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NOSIP | GRCh38.p7 | 19:49566662 | TGTGTGCATTTAAAA[C/T]GTGGTTAGAGGCTGG | 51070 |
rs181579414 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49566263 | CTGACCTCGTGATCC[A/G]CCCACCTCGGCTTCC | 51070 |
rs181793044 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NOSIP | GRCh38.p7 | 19:49576848 | AAGATCGCACCATTG[A/C]ACTCCAGCCTAGGCA | 51070 |
rs181909789 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49556094 | AGGCAGGGAAGGGGC[A/G]GGGCCTTGAAAAGGA | 51070 |
rs182029327 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NOSIP | GRCh38.p7 | 19:49571345 | CCAGAAAGCGTGAGC[A/G]CCTCCAACCAAGGGT | 51070 |
rs182040384 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | NOSIP | GRCh38.p7 | 19:49556139 | CCTAGGAGAGCGGAG[G/T]GGGGGAAGGGCGGGG | 51070 |
rs182199119 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NOSIP | GRCh38.p7 | 19:49566969 | TACAGGCGCGCACCA[C/T]CATGCCCAGCTAATT | 51070 |
rs182230145 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49561094 | CTTCCCCTCTCATAT[C/T]TGTAAGCTCTGACTG | 51070 |
rs182279802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49574781 | TGCAGCGGCGGATCT[C/T]GCCTCCCAGGCCCAA | 51070 |
rs182524965 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565431 | TTAGACAGTTATGCT[G/T]TCTGTACTTCTCTGT | 51070 |
rs182657161 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSIP | GRCh38.p7 | 19:49557974 | AAAGCCCAATAAGCA[C/T]GTGACCTGTAGTGTT | 51070 |
rs182662183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578058 | CACAACTCTGTCAAC[A/G]TACTAAACACCACTG | 51070 |
rs182926210 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NOSIP | GRCh38.p7 | 19:49564093 | TGACACTGCAACACT[A/G]AATTAGTAGTAATTT | 51070 |
rs183080182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49558179 | TGATTTGGCCGTCAG[C/T]CCGTTTTACAGACGA | 51070 |
rs183080864 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NOSIP | GRCh38.p7 | 19:49572927 | GCAGTGAGCCAAGAT[C/T]GGGCCACTGCACTCC | 51070 |
rs183087991 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49578951 | TTAAAAAAAAAAAGA[A/C]AGAAAACAGAAGCAG | 51070 |
rs183108776 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | NOSIP | GRCh38.p7 | 19:49567364 | CTGACCTCGTGATCC[A/G]CCCGCCTCGGCCTCC | 51070 |
rs183177634 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOSIP | GRCh38.p7 | 19:49568313 | TGTGATGTGGTGGAA[A/G]GAGGGTTATTTGAGA | 51070 |
rs183334011 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580022 | GAATCCCTGCACCAA[C/T]CCCGAAAGGGAAGGG | 51070 |
rs183570803 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49558749 | ATCTGGGCTGAAATC[A/G]GTGAGAAGGATTTGG | 51070 |
rs183715696 | snp | C/T | 0.00257143 | 0.0357645 | intron-variant | NOSIP | GRCh38.p7 | 19:49555833 | CCGCCCTGGGGGAGG[C/T]AGAGAGAAGGACGAG | 51070 |
rs183724242 | snp | A/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576100 | AGATCACGCCACTGC[A/T]CTCCAGCCTGAGCGA | 51070 |
rs183866174 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | NOSIP | GRCh38.p7 | 19:49566421 | TCAAGTGATCCTCCC[A/C]CCATAGCTTCCCAAG | 51070 |
rs184048993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565044 | ACTTGGGGAGGCCAA[A/G]GCAGGAGGATTGTTT | 51070 |
rs184270268 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | NOSIP | GRCh38.p7 | 19:49569848 | CAACAAAAAAGAACA[A/C]TTGCAGGTGGGGCGA | 51070 |
rs184331064 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49559371 | AAAACAAACAAAAAC[A/G]CCAGGTGTGGTAGTG | 51070 |
rs184337172 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49581809 | AAGAAAGATAAGCTG[C/T]CTGCTCCTTGCTTTC | 51070 |
rs184596678 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555602 | TCAATATGCTTAGCC[C/G]GCTCTTTCAAACTCC | 51070 |
rs184742006 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575711 | TAGCATAAAAGCAGC[C/G]ACAGACACACAAACG | 51070 |
rs184778036 | snp | C/T | | | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49582163 | GGAGAATCGCTTGAA[C/T]CCAGGAGGCAGAGGT | 51070 |
rs184849064 | snp | A/G | 0.00358779 | 0.0422022 | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555184 | GTGGCGCACTCACAC[A/G]GTCTTGGCTTAGACT | 51070 |
rs184855346 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575065 | AGAGGGGGTTTCACC[A/G]CGTTAGCCAGGATGG | 51070 |
rs185048862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49557986 | GCATGTGACCTGTAG[C/T]GTTTCCTGAGCGCCA | 51070 |
rs185055513 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578146 | TTTTTTTTTTTGAGA[G/T]GGAGTTATGCTCTTT | 51070 |
rs185489835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49563797 | ACTGTGCCCAGCCTG[A/G]AAATACTTGCTTTAG | 51070 |
rs185744970 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49566050 | TTTTTGAGACAGTCT[C/T]GCTCTGTCGTCCAGG | 51070 |
rs186035287 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49566768 | CTTCACTTGACCAGC[C/G]TTAAAAATATAAATA | 51070 |
rs186061137 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | NOSIP | GRCh38.p7 | 19:49572183 | TGATCTCGGCTCACT[G/T]CAACCTTCACCTCCC | 51070 |
rs186237221 | snp | C/T | 0.00220056 | 0.0330974 | intron-variant | NOSIP | GRCh38.p7 | 19:49556465 | ACTCTGATCAGGGGC[C/T]TTCCTGGGGACCTAC | 51070 |
rs186342728 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSIP | GRCh38.p7 | 19:49571305 | CTTTGATTTTTAAAA[C/T]TCAGTGATTTTTAAG | 51070 |
rs186412155 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577041 | CAAAGATCTACAAAT[A/G]GCCAATAAGCATGTT | 51070 |
rs186451361 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576664 | CCGAGGTGGGCGGAT[C/G]ACCTGAGGTTGGGAA | 51070 |
rs186461575 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49567272 | GGACTACAGGCACCC[A/G]CCACCACACCGTATA | 51070 |
rs187087200 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564411 | GTGAGCCAAGATCAC[A/G]CCACGGCACTCTAGC | 51070 |
rs187205198 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575066 | GAGGGGGTTTCACCA[C/T]GTTAGCCAGGATGGT | 51070 |
rs187228088 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565593 | ATCTCTACAAAAAAA[A/T]ATATATATATAAAAA | 51070 |
rs187392025 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49556102 | AAGGGGCGGGGCCTT[A/G]AAAAGGAAGGAGGAG | 51070 |
rs187609513 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49567854 | TTTTTTTGCATTTTT[A/T]TTTTAGTAGAGACAG | 51070 |
rs187824466 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NOSIP | GRCh38.p7 | 19:49569487 | ACAGGTGTGAGCCAC[C/T]GTGCCTGGCCTACAA | 51070 |
rs187859021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49568435 | ATGTGTGCTTTGTGT[A/G]TTCCCACACACACAC | 51070 |
rs188025895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49573130 | AGAGAGGCACAGAGG[C/T]GGTGCCCTAGGTTAT | 51070 |
rs188099064 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49560017 | GCTCAGTCGAATGTT[C/T]TGGGTCCCATAGCCC | 51070 |
rs188103413 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49582011 | TTGGGAGGCCGAGGC[A/G]GGTGGATCACTTGAG | 51070 |
rs188373996 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555485 | GCTGGTCTCGAACTC[C/T]TGACCTCAAGTGATA | 51070 |
rs188435487 | snp | A/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49556087 | GGGCTGGAGGCAGGG[A/C]AGGGGCGGGGCCTTG | 51070 |
rs188443215 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576210 | TTACAAAAGTCAGAT[A/C]TCTCCTGGCTGTTGT | 51070 |
rs188502013 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NOSIP | GRCh38.p7 | 19:49559214 | AATCTAGTAGAGACT[A/G]GATTTGAGCTTCCAG | 51070 |
rs188639582 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565186 | GAGTCTGAGATGGAT[C/G]ACCTGAGCCCAGGGA | 51070 |
rs188640068 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NOSIP | GRCh38.p7 | 19:49566427 | GATCCTCCCACCATA[C/G]CTTCCCAAGTAGCTG | 51070 |
rs188763601 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49566220 | GAAAACGGGGTTTCA[C/G]CGTGTTAGCCAGGAT | 51070 |
rs188793066 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580038 | CCCGAAAGGGAAGGG[A/G]CTGTCAAAAAGGTGA | 51070 |
rs188830230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49579328 | GGTCATTGGTTTGGA[C/T]TGAGCTCCTGCACTA | 51070 |
rs189087320 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49570151 | TCTTGCAGACAAAAG[C/G]CTCCACATGACACAT | 51070 |
rs189101222 | snp | A/G/T | 0.00597247 | 0.0543191 | intron-variant | NOSIP | GRCh38.p7 | 19:49562284 | CTGCCACCACGCCTG[A/G/T]CTAATTTTTTTGTAT | 51070 |
rs189104424 | snp | G/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49558370 | TCTCCTGCCTCAGCT[G/T]CCTGAGTAGCTGGGA | 51070 |
rs189287888 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49570524 | AGAACCTTCCTATCA[C/T]GCTAAATACCCCCTC | 51070 |
rs189312617 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565892 | TCATCCCTGAATGAA[C/T]ACAACTCTTGGATTT | 51070 |
rs189562646 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NOSIP | GRCh38.p7 | 19:49563900 | GTTCCTAGGCTATAA[C/G]AGTCCAATACTCTTC | 51070 |
rs189664765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575720 | AGCAGCCACAGACAC[A/G]CAAACGGGCATGGCT | 51070 |
rs189714624 | snp | G/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578168 | ATGCTCTTTTGCCCA[G/T]GCTGGAGTGAAGTGG | 51070 |
rs189822945 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49556120 | AAGGAAGGAGGAGGC[A/G]GGGCCTAGGAGAGCG | 51070 |
rs189908122 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NOSIP | GRCh38.p7 | 19:49558165 | CCTGCTGTGTCCTCT[A/G]ATTTGGCCGTCAGCC | 51070 |
rs189918179 | snp | C/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555646 | GGAGCACTGTTTGCA[C/G]GGCCCTGCATCCTCG | 51070 |
rs190086467 | snp | G/T | | | intron-variant, utr-variant-5-prime | NOSIP | GRCh38.p7 | 19:49576824 | GGGAGGCGAAGGTCG[G/T]GATGAGCCAAGATCG | 51070 |
rs190494985 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NOSIP | GRCh38.p7 | 19:49567315 | TTTAGTGGAAACGGG[G/T]TTTCACTGTGTTAGC | 51070 |
rs190722493 | snp | C/G | 6.95822e-05 | 0.00589799 | intron-variant | NOSIP | GRCh38.p7 | 19:49560731 | GGACTGTGGTTACCG[C/G]AGGCAGGCAGCACAG | 51070 |
rs190905080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49573412 | GAGCTACCTCCGTTA[C/T]AGCCCGTCCCTCGGT | 51070 |
rs190947295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49571344 | ACCAGAAAGCGTGAG[C/T]GCCTCCAACCAAGGG | 51070 |
rs191102020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577308 | TCATGCCTGTAATCC[C/T]AGCACTTTGGGAGGC | 51070 |
rs191315069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565736 | GCTCTCCAGCCTGGG[C/T]AATAGAGTGAGAACC | 51070 |
rs191362534 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NOSIP | GRCh38.p7 | 19:49568090 | GGCTTACAGAGAAAA[C/G]AGGATTGTGTCACAA | 51070 |
rs191469119 | snp | A/C/G/T | 0.0027921 | 0.0372689 | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49582133 | GTAATCTCAACTACC[A/C/G/T]GGGAGGCTGAGTCAG | 51070 |
rs191741403 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | NOSIP | GRCh38.p7 | 19:49559293 | AACAATGTGTGCCAC[A/G]TATTGTTGCAGCCAC | 51070 |
rs191775218 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NOSIP | GRCh38.p7 | 19:49572795 | CCTGGCCAATGTGGC[A/G]AAACCCTGTCTCTAC | 51070 |
rs191985623 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOSIP | GRCh38.p7 | 19:49569535 | CATTTGGCCGGGCAC[A/G]GTGGCTCACACCTGT | 51070 |
rs192157865 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565199 | ATCACCTGAGCCCAG[G/T]GAGGTCAAGGCTGCA | 51070 |
rs192211350 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564467 | TCAAAAAAAAAAAAA[A/C]AAAAAAAAACAAAAT | 51070 |
rs192444963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575024 | CCCGCCACCATGCCC[A/G]GCTAATTTTTTTGTA | 51070 |
rs192840375 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NOSIP | GRCh38.p7 | 19:49558660 | CACATGTACAGCTAC[A/G]ACTATGCTAAGTGCT | 51070 |
rs192917416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575586 | ACATTCAATTTCCTG[A/G]TTCTAGGAAGTCAGA | 51070 |
rs192968076 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575919 | GGCAGATCGTGAGGT[C/G]AGGAGATTGAGACCA | 51070 |
rs193050797 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579593 | GATTTTCTCAGCCCT[C/T]TGTCTCTGAAAACAA | 51070 |
rs193159348 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555525 | CGGCCTCCGAAAGTG[C/T]TGGGATTACAGGCGT | 51070 |
rs193244408 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565899 | TGAATGAACACAACT[A/C]TTGGATTTGACACCT | 51070 |
rs199508401 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49568621 | ACTCCAGCAAATCAA[A/G]AAGAAAATTACAGCC | 51070 |
rs199548969 | snp | C/T | 0.000182788 | 0.00955826 | intron-variant | NOSIP | GRCh38.p7 | 19:49556288 | GGGGCCTTGGAGTGC[C/T]GGGGGAAGGGGAGGG | 51070 |
rs199597353 | snp | C/T | 0.000520788 | 0.0161283 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49560623 | CCCCAGCCCTGCACC[C/T]GTGTCCTTCTTCTTC | 51070 |
rs199639083 | in-del | -/TG | | | intron-variant | NOSIP | GRCh38.p7 | 19:49568809 | AATAGTTTGTTTGTT[-/TG]TTTTTTTTTTTGAGA | 51070 |
rs199644035 | in-del | -/A | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579784 | AATCTCTTTAAGTTT[-/A]AAAAAATACAGCAAG | 51070 |
rs199673125 | in-del | -/GG | | | intron-variant | NOSIP | GRCh38.p7 | 19:49556134 | GGGGCCTAGGAGAGC[-/GG]GGAGGGGGGGAAGGG | 51070 |
rs199677305 | snp | C/T | | | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555270 | TTTTTTTTTTTTTTT[C/T]TTCTTTGAGATGGAG | 51070 |
rs199751614 | snp | A/C | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564465 | TCTCAAAAAAAAAAA[A/C]AAAAAAAAAAACAAA | 51070 |
rs199755418 | in-del | -/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577764 | GCAAGGCCGTGTCTC[-/G]GGGAAAAAAAAAAAA | 51070 |
rs199804285 | snp | A/G | 0.000199706 | 0.00999065 | missense | NOSIP | GRCh38.p7 | 19:49557188 | CGCACATGGTCCTGC[A/G]AGGCCGCCCGCTGAA | 51070 |
rs199918553 | in-del | -/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49568806 | AAAAATAGTTTGTTT[-/G]TTTGTTTTTTTTTTT | 51070 |
rs200035568 | in-del | -/GCGCAGA | 0.00795532 | 0.062565 | intron-variant | NOSIP | GRCh38.p7 | 19:49555997 | TGGACAGGGCGCAGG[-/GCGCAGA]GCGCAGAGAAGAGGG | 51070 |
rs200095228 | snp | A/C/G | 6.26964e-05 | 0.00559866 | intron-variant | NOSIP | GRCh38.p7 | 19:49557035 | GCCGCCCCCTGGGCC[A/C/G]GCCCAGCCCGCGGCG | 51070 |
rs200191784 | in-del | -/GGGCCTTAAAAATAGGGCAGGGGCA | 0.26518 | 0.249539 | intron-variant | NOSIP | GRCh38.p7 | 19:49556094 | GGCAGGGAAGGGGCG[-/GGGCCTTAAAAATAGGGCAGGGGCA]GGGCCTTGAAAAGGA | 51070 |
rs200238455 | snp | A/C/G | 0.000365897 | 0.0135213 | missense | NOSIP | GRCh38.p7 | 19:49557225 | TCTGCTCCTCGCGCC[A/C/G]GGTGCCCCGCTGCTT | 51070 |
rs200288824 | in-del | -/A | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565757 | GTGAGAACCTGTCTC[-/A]AAAAGAAAAAAAAAA | 51070 |
rs200291402 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49570122 | AAATAAAGAAAGAAT[C/T]AAATATAAAGAACTC | 51070 |
rs200454878 | snp | C/T | 1.71563e-05 | 0.0029288 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49556557 | GACTCACGAGGGCCG[C/T]AGCACAGCGCAGGGG | 51070 |
rs200491222 | snp | A/G | 0.00449352 | 0.0471865 | intron-variant | NOSIP | GRCh38.p7 | 19:49555843 | GGAGGTAGAGAGAAG[A/G]ACGAGGTAGAGGCCG | 51070 |
rs200554064 | in-del | -/GA | | | intron-variant | NOSIP | GRCh38.p7 | 19:49556136 | GGGCCTAGGAGAGCG[-/GA]GGGGGGGAAGGGCGG | 51070 |
rs200565147 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565770 | CTCAAAAGAAAAAAA[A/G]AAGAAAGAAAGAAAG | 51070 |
rs200609465 | in-del | -/TTC | | | intron-variant | NOSIP | GRCh38.p7 | 19:49563494 | TTTTGTGCTTGAAAA[-/TTC]TTTTTTTTTTTTTTG | 51070 |
rs200657042 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577767 | AAGGCCGTGTCTCGG[A/G]AAAAAAAAAAAAAAA | 51070 |
rs200660249 | in-del | -/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49568810 | ATAGTTTGTTTGTTT[-/G]TTTTTTTTTTTGAGA | 51070 |
rs200746730 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NOSIP | GRCh38.p7 | 19:49568814 | TTTGTTTGTTTGTTT[G/T]TTTTTTTGAGACAGA | 51070 |
rs200860162 | snp | C/G/T | 0.000117807 | 0.00767405 | utr-variant-3-prime | NOSIP | GRCh38.p7 | 19:49555732 | ACCCAAGCCGGTTTA[C/G/T]TTGGTCTCCCGCACA | 51070 |
rs201030429 | in-del | -/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49568806 | AAAATAGTTTGTTTG[-/T]TTTGTTTTTTTTTTT | 51070 |
rs201090674 | snp | A/G | 0.000415245 | 0.0144031 | intron-variant | NOSIP | GRCh38.p7 | 19:49560716 | GAAGGGACAGTGGCA[A/G]GACTGTGGTTACCGG | 51070 |
rs201096061 | in-del | -/TTTAT | | | intron-variant | NOSIP | GRCh38.p7 | 19:49573793 | TTTATTTTATTTTAT[-/TTTAT]GTATGTATGTATGTA | 51070 |
rs201132953 | snp | A/G | 0.00119558 | 0.0244205 | intron-variant | NOSIP | GRCh38.p7 | 19:49560698 | CCGCGTCATCCTAGG[A/G]AGGAAGGGACAGTGG | 51070 |
rs201174800 | snp | A/C | | | synonymous-codon | NOSIP | GRCh38.p7 | 19:49556383 | GTCCACCATGTCCTT[A/C]CGAATCAGCTTCTCC | 51070 |
rs201226996 | in-del | -/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576586 | TGAGACCTTGTCTCT[-/G]GGGAAAAAAAAAAAA | 51070 |
rs201414407 | snp | A/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564361 | GGGGAGGCTGAGGCA[A/T]GAGAATCGCTTGAAC | 51070 |
rs201434699 | snp | C/T | | | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49582219 | GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC | 51070 |
rs201590783 | in-del | -/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565762 | GAACCTGTCTCAAAA[-/G]AAAAAAAAAAGAAAG | 51070 |
rs201805026 | in-del | -/AGAA | | | intron-variant | NOSIP | GRCh38.p7 | 19:49570120 | AAAATAAAGAAAGAA[-/AGAA]TAAAATATAAAGAAC | 51070 |
rs201833397 | snp | A/G | 0.000291523 | 0.0120696 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49556572 | CAGCACAGCGCAGGG[A/G]GTGGCGTTGCTCAGG | 51070 |
rs201855238 | in-del | -/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49568802 | AAAAAAAAATAGTTT[-/G]TTTGTTTGTTTTTTT | 51070 |
rs201976944 | snp | C/G | 2.13108e-05 | 0.00326419 | missense | NOSIP | GRCh38.p7 | 19:49557144 | TGAGGGGCCGGCTCA[C/G]GATAGCCGACTCCTT | 51070 |
rs202035964 | in-del | -/A | | | intron-variant | NOSIP | GRCh38.p7 | 19:49556137 | GGCCTAGGAGAGCGG[-/A]GGGGGGGAAGGGCGG | 51070 |
rs202134417 | in-del | -/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49556137 | GCCTAGGAGAGCGGA[-/G]GGGGGGGAAGGGCGG | 51070 |
rs202157014 | in-del | -/AAT | | | intron-variant | NOSIP | GRCh38.p7 | 19:49574050 | ATTTTTAGTAGAGAC[-/AAT]GGGGTTTCACCATGT | 51070 |
rs202224889 | in-del | -/TC | | | intron-variant | NOSIP | GRCh38.p7 | 19:49563495 | TTTGTGCTTGAAAAT[-/TC]TTTTTTTTTTTTTTG | 51070 |
rs367544457 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555517 | GCTAGCCTCGGCCTC[C/T]GAAAGTGCTGGGATT | 51070 |
rs367578345 | snp | G/T | 3.41869e-05 | 0.00413428 | intron-variant | NOSIP | GRCh38.p7 | 19:49556449 | AGGCCGAAGGCGGGA[G/T]ACTCTGATCAGGGGC | 51070 |
rs367745420 | snp | G/T | | | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555258 | GTTCTATTCAGGTTT[G/T]TTTTTTTTTTTCTTC | 51070 |
rs367755887 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49566687 | GGCTGGGCTGAGTGC[A/G]GCAATGTTTACAACT | 51070 |
rs367797286 | in-del | -/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579802 | AAAATACAGCAAGTA[-/T]GGCAAAAATAATCAT | 51070 |
rs367819669 | in-del | -/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49568225 | TCCAAAAATATGGCA[-/G]GTTGACCTTGACAAA | 51070 |
rs367897337 | snp | A/G | 1.69507e-05 | 0.0029112 | intron-variant | NOSIP | GRCh38.p7 | 19:49555834 | CGCCCTGGGGGAGGT[A/G]GAGAGAAGGACGAGG | 51070 |
rs367946353 | multinucleotide-polymorphism | AA/GG | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565769 | TCTCAAAAGAAAAAA[AA/GG]AAGAAAGAAAGAAAG | 51070 |
rs368191756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49572188 | TCGGCTCACTGCAAC[C/T]TTCACCTCCCCGATT | 51070 |
rs368395117 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49572199 | CAACCTTCACCTCCC[C/T]GATTCAAGTGATTCT | 51070 |
rs368425907 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49570384 | CTCTCCCCCTACTGG[C/T]GTCTTCTCAGAAGCC | 51070 |
rs368503120 | snp | A/C | 4.03519e-05 | 0.00449158 | missense | NOSIP | GRCh38.p7 | 19:49556947 | GGGCAGCACTTTGTC[A/C]TTGTCCTTACTTGGA | 51070 |
rs368607204 | snp | A/G | | | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49582449 | CTGGCTAATTTTTGT[A/G]TGACTCCTGTGAAAA | 51070 |
rs368634753 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NOSIP | GRCh38.p7 | 19:49562684 | TCAAGAGATCGAGAC[C/T]ATCCTGGCCAACATG | 51070 |
rs368721012 | snp | C/T | 0.000155988 | 0.00883004 | intron-variant | NOSIP | GRCh38.p7 | 19:49557034 | TGCCGCCCCCTGGGC[C/T]CGCCCAGCCCGCGGC | 51070 |
rs368759917 | snp | A/C/G | 3.41952e-05 | 0.00413481 | intron-variant | NOSIP | GRCh38.p7 | 19:49556514 | GCCCCGCAGGTTCCC[A/C/G]AGTGGTCCCTTCCCT | 51070 |
rs368973496 | in-del | -/TT | | | intron-variant | NOSIP | GRCh38.p7 | 19:49572110 | AATTTTCTTTTTTTT[-/TT]CTTTTTTTTTTGAGA | 51070 |
rs368976284 | snp | A/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49569339 | GCTGGGACTACAGGC[A/C]CCTGCCACCACACCC | 51070 |
rs369009521 | snp | A/G | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49581027 | ACAGGGATTTACTGC[A/G]GCACTGCCCAGCTGT | 51070 |
rs369170296 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOSIP | GRCh38.p7 | 19:49558232 | TGAGGTGATGTCAAT[C/T]CACGTAGCACATCTT | 51070 |
rs369266633 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49567085 | CCTCCCAAAGTGCTG[A/G]GATTATAGGCATGAG | 51070 |
rs369276743 | snp | A/G | 0.030278 | 0.119257 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49574988 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 51070 |
rs369833126 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575085 | AGCCAGGATGGTCTC[C/G/T]ATCTCCTGACTTCGT | 51070 |
rs369839191 | snp | C/T | 1.72392e-05 | 0.00293586 | missense | NOSIP | GRCh38.p7 | 19:49556594 | TTGCTCAGGCTGTCG[C/T]GGGTCACGGCACACA | 51070 |
rs369863958 | snp | A/G | 0.000146431 | 0.00855535 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49560644 | CTTCTTCTTCTCGTG[A/G]TAGGTGTAGACGGCC | 51070 |
rs369949420 | snp | C/T | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579782 | TTAATCTCTTTAAGT[C/T]TAAAAAAATACAGCA | 51070 |
rs370045117 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | NOSIP | GRCh38.p7 | 19:49556865 | GTGCCGGGGCGCTGT[G/T]GGGGCTCACCGGCTT | 51070 |
rs370070206 | snp | A/G | 0.00011536 | 0.00759387 | missense | NOSIP | GRCh38.p7 | 19:49558908 | TCACCTTCATCTGCC[A/G]GGCAATCTCCTTCTT | 51070 |
rs370113967 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555560 | CACCGTGCCTGGCCA[C/G]ATTTTGTTCTTAATG | 51070 |
rs370166035 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | NOSIP | GRCh38.p7 | 19:49570842 | GCAGTATTTGGCTCT[-/G]GGCACCTCGGCTTTC | 51070 |
rs370541246 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49570552 | CTCACGCCCCTTCCC[A/G]ATCAATGTGCCCCCT | 51070 |
rs370691509 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | NOSIP | GRCh38.p7 | 19:49561168 | CACTTAGCTAAGGCT[G/T]GACACTTAGCTAAGG | 51070 |
rs370740006 | snp | A/G | 1.85675e-05 | 0.00304687 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555700 | ACGCCGCGAATGAAG[A/G]CGCCACGTCGTTGCG | 51070 |
rs370833946 | snp | C/G | 2.13509e-05 | 0.00326726 | missense | NOSIP | GRCh38.p7 | 19:49559934 | CTGTTCCCAGCTCAC[C/G]TGACAACAGGATCGT | 51070 |
rs371060180 | snp | A/G | 0.000230455 | 0.0107319 | intron-variant | NOSIP | GRCh38.p7 | 19:49557254 | TTCTCGTAGGCCTGC[A/G]TCGGGGAAAGTGGGC | 51070 |
rs371390647 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49555952 | GGAGTAGGAGTTGGG[A/G]AGGGGGCGAGGCGAC | 51070 |
rs371482842 | snp | A/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49573986 | TGCCTCAGCCTCCCA[A/C]GTAGCTGGGATTACA | 51070 |
rs371655480 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49571616 | GGGACTCAGACCCAG[A/G]CAGCCAGGCTCTGGA | 51070 |
rs371866715 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49562599 | AACAAAGAAGTTGAT[A/G]GCCAGGTGCAGTGGC | 51070 |
rs371941851 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49557145 | GAGGGGCCGGCTCAC[A/G]ATAGCCGACTCCTTC | 51070 |
rs372098818 | snp | C/T | 9.40689e-05 | 0.00685752 | intron-variant | NOSIP | GRCh38.p7 | 19:49559913 | CCCACCCAGACCTAC[C/T]CATCCCTGTTCCCAG | 51070 |
rs372106102 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49556704 | CGACATGCGCAGGGG[C/T]TTCCCTGACATGGGG | 51070 |
rs372577019 | snp | C/T | 3.29701e-05 | 0.00406005 | intron-variant | NOSIP | GRCh38.p7 | 19:49558874 | CCTGCCTCCGTGTGC[C/T]GCCTCCTCCCCATCC | 51070 |
rs372589310 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49567373 | TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 51070 |
rs372658148 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49578795 | GGGACTACAGGTGCC[C/T]GCCATCATGCCCGGC | 51070 |
rs372934271 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576060 | GAATGGCATGAACCC[A/G]GGAGGTGGAGCTTGC | 51070 |
rs372998588 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578287 | AGCCACCATGACCAG[C/T]CAATTTTTGTATTTT | 51070 |
rs373028786 | snp | C/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564308 | AAATACAAAAAGTTA[C/G]CTGGTCGTGGTGGTG | 51070 |
rs373153641 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49562428 | TGTGCCTGGCCCCTG[C/T]AGGCTTTTTTATCCC | 51070 |
rs373160388 | snp | A/C | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580861 | GGACTAATCACTTCC[A/C]CTAGAGATCGGGAAG | 51070 |
rs373372386 | snp | A/G | 4.66103e-05 | 0.00482731 | missense | NOSIP | GRCh38.p7 | 19:49560657 | TGGTAGGTGTAGACG[A/G]CCCCTGCGGTGCAGT | 51070 |
rs373447628 | in-del | AAA/GG | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565768 | GTCTCAAAAGAAAAA[AAA/GG]AAGAAAGAAAGAAAG | 51070 |
rs373563128 | snp | A/T | 0.000340245 | 0.0130387 | intron-variant | NOSIP | GRCh38.p7 | 19:49560064 | GAGATGGGCAGAGTG[A/T]TGGAGGGGCGGAGCA | 51070 |
rs373729460 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49569836 | CAACAACAACAACAA[C/T]AAAAAAGAACACTTG | 51070 |
rs373787198 | snp | A/T | | | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555250 | GCATTTGCGTTCTAT[A/T]CAGGTTTTTTTTTTT | 51070 |
rs373825269 | snp | C/G | 0.000423293 | 0.0145419 | intron-variant | NOSIP | GRCh38.p7 | 19:49557060 | GCGGCGCCCCGCCCC[C/G]CAACCCACAAGAAGC | 51070 |
rs373851057 | snp | A/G | 3.54126e-05 | 0.00420774 | intron-variant | NOSIP | GRCh38.p7 | 19:49555866 | AGAGGCCGGCCCGGG[A/G]GTGACCAGTGGGGCT | 51070 |
rs373984549 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NOSIP | GRCh38.p7 | 19:49561170 | CTTAGCTAAGGCTTG[A/G]CACTTAGCTAAGGCT | 51070 |
rs374216100 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49581351 | AACGGGGATCAGGCC[G/T]GGTTACCGGGAGTGG | 51070 |
rs374281185 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49571419 | GCTCTCCTGCCCCAC[A/G]CTATATTGTCTCTTT | 51070 |
rs374288879 | snp | A/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49555953 | GAGTAGGAGTTGGGG[A/T]GGGGGCGAGGCGACC | 51070 |
rs374367134 | snp | A/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49562196 | GCATGATCTTGGCTC[A/C]CTGAAACCTCTGCCT | 51070 |
rs374814242 | snp | C/T | 1.64808e-05 | 0.00287057 | intron-variant | NOSIP | GRCh38.p7 | 19:49558889 | CGCCTCCTCCCCATC[C/T]CCATCACCTTCATCT | 51070 |
rs375018982 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49569480 | TGGGATTACAGGTGT[A/G]AGCCACCGTGCCTGG | 51070 |
rs375041684 | snp | C/G | 3.52877e-05 | 0.00420031 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555710 | TGAAGGCGCCACGTC[C/G]TTGCGCACCCAAGCC | 51070 |
rs375086867 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578025 | AAAATATTCTTAAAA[C/T]GATAGTGTTGATGGT | 51070 |
rs375284673 | snp | A/G | 1.71466e-05 | 0.00292797 | intron-variant | NOSIP | GRCh38.p7 | 19:49556439 | CACTACGGTGAGGCC[A/G]AAGGCGGGAGACTCT | 51070 |
rs375469093 | snp | G/T | | | missense | NOSIP | GRCh38.p7 | 19:49557132 | CTGTGAAAGGGTTGA[G/T]GGGCCGGCTCACGAT | 51070 |
rs375479704 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49568336 | ATTTGAGATCTGATG[A/G]AAAGTCCTAGTACCA | 51070 |
rs375781457 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NOSIP | GRCh38.p7 | 19:49558030 | GGAAGAGGGGGACAG[A/G]CCCACTGTGCCTCAA | 51070 |
rs375841154 | snp | A/G | 0.0001561 | 0.0088332 | intron-variant | NOSIP | GRCh38.p7 | 19:49560704 | CATCCTAGGGAGGAA[A/G]GGACAGTGGCAGGAC | 51070 |
rs376009859 | snp | A/C | 3.41332e-05 | 0.00413103 | intron-variant | NOSIP | GRCh38.p7 | 19:49556476 | GGGCCTTCCTGGGGA[A/C]CTACTGGCCCCAAAG | 51070 |
rs376259890 | snp | A/C/G | 2.11031e-05 | 0.00324824 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555676 | GCCTGCCCTGTCCCC[A/C/G]GGGCGCCCACGCCGC | 51070 |
rs376400410 | snp | A/G | 0.000147048 | 0.00857335 | missense | NOSIP | GRCh38.p7 | 19:49556729 | ATGGGGCAGGTCACC[A/G]TGCGGGACTGCAAGG | 51070 |
rs376440318 | snp | C/G | 0.000253192 | 0.0112486 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49556662 | CACGGAGCTGTCTAG[C/G]GGTGTGAAGTGCACG | 51070 |
rs376489455 | snp | C/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49562993 | CAAAGGATACAATTT[C/G]CAGCAACGTAAATGT | 51070 |
rs376513824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49561742 | CAAAAATTAGCTGGG[C/T]GTGGTGGCACACGCC | 51070 |
rs376575345 | snp | A/C/G | 4.93778e-05 | 0.00496855 | intron-variant | NOSIP | GRCh38.p7 | 19:49556998 | TTGGACATCATCTGT[A/C/G]GGGGAAGGAAGGGAC | 51070 |
rs376597835 | snp | C/T | 4.82812e-05 | 0.00491307 | splice-donor-variant, missense | NOSIP | GRCh38.p7 | 19:49557089 | GCCCAACCTGAGTCA[C/T]CTGGGCTGGTGCCCG | 51070 |
rs376666447 | snp | C/T | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580830 | AGGTTTTGAGTCTCT[C/T]CAAGCCCAAATTTAA | 51070 |
rs376672989 | in-del | -/GT | 0.475081 | 0.108804 | intron-variant | NOSIP | GRCh38.p7 | 19:49556174 | CAGGAGAAAGCGGGG[-/GT]GGGGGGGGCGGCCTT | 51070 |
rs377166551 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOSIP | GRCh38.p7 | 19:49563406 | GCCTTGAACTCCTGG[A/G]CTCAAGTGAACTCCT | 51070 |
rs377181535 | snp | A/G | 0.000658882 | 0.0181385 | intron-variant | NOSIP | GRCh38.p7 | 19:49560597 | ACACAGCCATGTCCC[A/G]CCTCTTCCCACCCCA | 51070 |
rs377235405 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | NOSIP | GRCh38.p7 | 19:49558393 | AGCTGGGATTACAGG[C/G]GCCCGCCATGCCCGG | 51070 |
rs377266050 | snp | A/T | 3.01391e-05 | 0.00388183 | intron-variant | NOSIP | GRCh38.p7 | 19:49559915 | CACCCAGACCTACCC[A/T]TCCCTGTTCCCAGCT | 51070 |
rs377270334 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49581358 | ATCAGGCCTGGTTAC[C/T]GGGAGTGGGGCGCCC | 51070 |
rs377297387 | in-del | -/CAGA | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564534 | AGGGTTGCAATTAGA[-/CAGA]GGGGTGCAGGCGAGG | 51070 |
rs377305328 | snp | C/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49562069 | CCTGAACCCACAGAG[C/G]CTGGGCAGCTTTCAC | 51070 |
rs377403094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49557682 | AGCCCGTGTTTGGGA[C/T]GGGGGATGTAGACTT | 51070 |
rs377407415 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | PRRG2, NOSIP | GRCh38.p7 | 19:49580582 | CGGAAAGGAGCACTA[C/T]TTTCCCCCTCCGCTC | 51070 |
rs377420219 | snp | A/G | | | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49582278 | CCTGTGAAAAGTTTT[A/G]TTTTGTTTTGTTTTT | 51070 |
rs377494105 | snp | G/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49570831 | CTTGACCCTCTGCAG[G/T]ATTTGGCTCTGGGCA | 51070 |
rs377562965 | snp | C/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564626 | CTTTGGAAAGCAACT[C/G]TCAGTATCTACTGAA | 51070 |
rs386810152 | multinucleotide-polymorphism | GA/TT | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565789 | AAAGAAAGAAAGAAA[GA/TT]AATGGCGGGGGAACC | 51070 |
rs397734674 | in-del | -/A | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577784 | AAAAAAAAAAAAAAA[-/A]GAAGTATTGATACAT | 51070 |
rs398034946 | in-del | -/T | 0 | 0 | intron-variant | NOSIP | GRCh38.p7 | 19:49561900 | GGCTTAGGCAATGTC[-/T]TTTTTTTTTTTTTTT | 51070 |
rs398059802 | in-del | -/AT | | | intron-variant | NOSIP | GRCh38.p7 | 19:49572690 | AATATATATATATAT[-/AT]GGCTGGGAGCAGTGG | 51070 |
rs527238181 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49569224 | TTTTTTTTGAGACGT[A/T]ATCTCGCTCTTTCAC | 51070 |
rs527304525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49562477 | AGGCTCAGGGCTCAC[A/G]CCTGTAATCCCAAAA | 51070 |
rs527304544 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49569818 | TGTCTCAAAAAACAA[A/C]AACAACAACAACAAC | 51070 |
rs527381552 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOSIP | GRCh38.p7 | 19:49572784 | TTCAAGACCAGCCTG[A/G]CCAATGTGGCGAAAC | 51070 |
rs527411661 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49563303 | GCCTCAGCCTCTCGA[C/G]TAGCTGGGACTACAG | 51070 |
rs527567706 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575948 | CATCCTGACTAACAC[G/T]GTGAAACCCCGTCTC | 51070 |
rs527708744 | snp | C/G | 0.000798403 | 0.0199641 | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49554975 | CAGGCTGCCACAGGT[C/G]GGGGCGTGATGCTCC | 51070 |
rs527838483 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NOSIP | GRCh38.p7 | 19:49566854 | CAGAGTCTCGCTGTC[A/G]CCCAGGCTGGAGTGC | 51070 |
rs527902187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49567411 | CAGGCGTGAGCCACC[A/G]TGCCCGGCCCCAAAA | 51070 |
rs528025199 | snp | C/T | 0.000901435 | 0.021211 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49560686 | GTTCTTGCCATGCCG[C/T]GTCATCCTAGGGAGG | 51070 |
rs528236761 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant, utr-variant-5-prime | NOSIP | GRCh38.p7 | 19:49574640 | GTTCAGGCTACCAGC[A/C]TTGTGGGGTTCTGGT | 51070 |
rs528334068 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49574152 | CAGGCATGAGCTACC[A/G/T]CGCCCAGTCTTGCTC | 51070 |
rs528357107 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49564054 | CTCATTCTCTCACAA[A/G]TACACCAGAGGCTCC | 51070 |
rs528425276 | snp | C/T | | | synonymous-codon | NOSIP | GRCh38.p7 | 19:49555793 | CTCCGCTTGCAGCTT[C/T]ACTCCGGAGCCCGCG | 51070 |
rs528454594 | snp | A/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49567933 | TCTGGCCACCTTGGC[A/T]TCTCAAAGTGCTGGG | 51070 |
rs528552573 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49573440 | GGTATTTCGGCTCCA[C/G]AGTAGGGGCCCTGGT | 51070 |
rs528619280 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49569455 | TGCCCGCCTCGGCCT[C/T]CCAAAGTGCTGGGAT | 51070 |
rs528680663 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49573931 | GTGGCACGATCTTGA[C/T]TCACTGCAACCTCCA | 51070 |
rs528843802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564685 | GCAATTCGTCTCCCA[C/T]GTATACACCTAACAG | 51070 |
rs528844653 | snp | C/G | 0.000399281 | 0.0141238 | missense | NOSIP | GRCh38.p7 | 19:49556664 | CGGAGCTGTCTAGCG[C/G]TGTGAAGTGCACGGG | 51070 |
rs528855553 | snp | C/T | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580014 | GAAAACGTGAATCCC[C/T]GCACCAACCCCGAAA | 51070 |
rs528912357 | in-del | -/TT | | | intron-variant | NOSIP | GRCh38.p7 | 19:49558423 | GCTCAATTTTTTTTT[-/TT]ATTTTTTTATTTTTA | 51070 |
rs529022611 | snp | G/T | | | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49582447 | GCCTGGCTAATTTTT[G/T]TATGACTCCTGTGAA | 51070 |
rs529071128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578199 | CATGATCTCAGCTCA[C/T]TGCAACCTCTGTCCC | 51070 |
rs529190303 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49570892 | CTGTTTTGTGGCCAA[C/G]AACTGAGGTTTCTAC | 51070 |
rs529416640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577471 | CTGAGGCAGGAGAGT[C/T]GCTCAAACCTGGGAG | 51070 |
rs529448992 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49562359 | GAGCTCCTGACCTCA[C/G]GTGATCCACCTGCCT | 51070 |
rs529514287 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555563 | CGTGCCTGGCCAGAT[G/T]TTGTTCTTAATGTGA | 51070 |
rs529739152 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49568343 | ATCTGATGGAAAGTC[C/G]TAGTACCAGATGTGG | 51070 |
rs529779077 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49561684 | TTCAGGAGTTCAAGA[G/T]CAGCCTGGCCAACAT | 51070 |
rs529845520 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NOSIP | GRCh38.p7 | 19:49569052 | GTGATCTGCCCGCCT[C/T]GGCCTCCCAGAGTGC | 51070 |
rs529936013 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49582345 | CAGTGGCACAGTCTC[A/G]GCTCACTGCAACCTC | 51070 |
rs530003857 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49559873 | CCCACGCACACAGCC[G/T]CCTCCTGGCGGTTCC | 51070 |
rs530062638 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49567365 | TGACCTCGTGATCCG[C/G]CCGCCTCGGCCTCCC | 51070 |
rs530108425 | snp | C/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575537 | GCTCTGAAGTAATCA[C/G]CTGACAGCTGAATGG | 51070 |
rs530111660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49560542 | AGACAGGGACAGAGG[A/G]AGCAAAACCTGGGGC | 51070 |
rs530112413 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | NOSIP | GRCh38.p7 | 19:49570670 | CCGACTTCCCCCTGA[-/C]CCCCCAAGCTTCTCA | 51070 |
rs530277692 | snp | G/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49569855 | AAAGAACACTTGCAG[G/T]TGGGGCGAGGTGGCT | 51070 |
rs530352669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49572286 | AATTTTTTGTATTTT[C/T]AGTAGAGATGGGGTT | 51070 |
rs530379193 | snp | G/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49559916 | ACCCAGACCTACCCA[G/T]CCCTGTTCCCAGCTC | 51070 |
rs530577676 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565547 | TGAGCTCAGGAGTTT[C/G]AGACTAGTCTGGGCA | 51070 |
rs530634904 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | PRRG2, NOSIP | GRCh38.p7 | 19:49580572 | GCCCCGACACCGGAA[A/G]GGAGCACTATTTTCC | 51070 |
rs530951128 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NOSIP | GRCh38.p7 | 19:49572544 | CAGCCTCCCAAGTAA[A/C]TGGAATTCCAGGCGT | 51070 |
rs531019250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49571652 | TCCTTTTAACTAGGT[A/G]ACAACTGTCAGTTTT | 51070 |
rs531060526 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564549 | CAGAGGGGTGCAGGC[A/G]AGGACATGGAGCTAC | 51070 |
rs531117133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578365 | CTGACCTCAGATGAT[C/T]CACCTGCCTTCACCT | 51070 |
rs531163244 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NOSIP | GRCh38.p7 | 19:49570734 | TGCCATCCGCTCCCC[A/C]GCCCCCACAACTGCC | 51070 |
rs531213394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49556008 | GCAGGGCGCAGAGAA[A/G]AGGGTAGAGAGTGGC | 51070 |
rs531335683 | snp | A/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576638 | ACCTGTAATCCCAGC[A/T]CTTTGGGAGGCCGAG | 51070 |
rs531488859 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49569300 | CCAGGTTCACACCAT[G/T]CTCCTGCCTCAGCCT | 51070 |
rs531617257 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577377 | TCCTGGCCAACATGG[C/T]GAAACCCCATCTCTA | 51070 |
rs531756027 | in-del | -/TTC | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49566019 | TTTTCTTTCTTTCTT[-/TTC]TTCTTCTTTTTTTTT | 51070 |
rs531948748 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49582181 | AGGAGGCAGAGGTCA[C/G]AGTGAGCTGAGATAG | 51070 |
rs532074008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49562261 | CAAATAGCAGGGATT[A/G]CAGGTGCCTGCCACC | 51070 |
rs532089791 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575099 | CTATCTCCTGACTTC[C/G]TGATCTGCCCACCTC | 51070 |
rs532131822 | snp | A/C | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564464 | ATCTCAAAAAAAAAA[A/C]AAAAAAAAAAAACAA | 51070 |
rs532259861 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NOSIP | GRCh38.p7 | 19:49572111 | ATTTTCTTTTTTTTT[C/T]CTTTTTTTTTTGAGA | 51070 |
rs532274629 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575879 | GCTCACGCCTGTAAT[A/C]CCAGCACTTTGGGAG | 51070 |
rs532287899 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | NOSIP | GRCh38.p7 | 19:49567467 | GCTCTCCATACAGAC[G/T]GCACAGGTCTATATA | 51070 |
rs532326283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49566177 | GGCGCTCGCCACCAC[A/G]CCTGGCTAATTTTTT | 51070 |
rs532378653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49559148 | GTGATAGTTTACTGC[A/G]GTGAAAGGATGCAGA | 51070 |
rs532494024 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49571858 | GGTGTGTTGGTGCGC[A/G]CCTGTGGTCCCAGCT | 51070 |
rs532516099 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49559663 | GGTAGGTCATGGGAA[A/G]TGTCCAAAGGTGAGC | 51070 |
rs532524642 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NOSIP | GRCh38.p7 | 19:49573112 | AATAGTTGCTATAAA[C/T]GAAGAGAGGCACAGA | 51070 |
rs532675195 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580438 | AAATCTTGCCCCAGT[A/C]TCCCTCAAGACCCCA | 51070 |
rs532705387 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579803 | AAATACAGCAAGTAT[A/G]GCAAAAATAATCATT | 51070 |
rs532731994 | snp | A/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49568297 | GCGCCTTGTGAATTA[A/C]TGTGATGTGGTGGAA | 51070 |
rs532734480 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49573613 | GCCATGACATCATGC[A/C]ATTAATACACTAATA | 51070 |
rs532775813 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49558142 | ATCTGCGTGTACCTC[C/T]CAGGTGCCCTGCTGT | 51070 |
rs532822500 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49572867 | TAGTCCCAGCTACTC[C/G]GGAGGCTGAGGCAGG | 51070 |
rs533114418 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564292 | ACCCCATCTGTACTA[A/C]AAATACAAAAAGTTA | 51070 |
rs533114520 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49571587 | GCATGTCCCAGCTGG[G/T]AAATGGCAGAGCTGG | 51070 |
rs533177357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564825 | ATCACATAATGGAAA[C/T]ACCCAGCAATGAGAC | 51070 |
rs533445779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578304 | AATTTTTGTATTTTT[A/G]GTAGAGATGAGGTTT | 51070 |
rs533507798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49571033 | CGAAGCTGGAGTGCA[A/G]TGGTGTGATCTCGGC | 51070 |
rs533555667 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSIP | GRCh38.p7 | 19:49555917 | CTAAGCGGGTCAAGG[C/T]GAAGCGGGTTGCTGG | 51070 |
rs533672724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49569972 | CAAAAATGAGCCAGT[C/T]GTGGTGGCCACCTGT | 51070 |
rs533793982 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555207 | CTTAGACTTGGACTT[C/T]CGGCCACTCAACCAA | 51070 |
rs533815092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49567879 | AGACAGGGTTCACCA[C/T]GTTGGCCAGGCTGAT | 51070 |
rs533876814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49561123 | TGAGGCCAAGGCGTG[A/G]ACCAGCCCAGTGATT | 51070 |
rs534305994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49582594 | CAACATGGTGAAACC[C/T]CATCTCTACTAAAAA | 51070 |
rs534313579 | snp | C/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565191 | TGAGATGGATCACCT[C/G]AGCCCAGGGAGGTCA | 51070 |
rs534329271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49561754 | GGGCGTGGTGGCACA[C/T]GCCAGTAATCCCAAC | 51070 |
rs534415595 | snp | C/T | 0.000149209 | 0.00863611 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49560032 | CTGGGTCCCATAGCC[C/T]GAGGCCGCTGGGGAC | 51070 |
rs534479255 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSIP | GRCh38.p7 | 19:49557413 | GTGTGAACCTTACTG[C/T]GTTGTATAGCCAGAC | 51070 |
rs534514457 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | NOSIP | GRCh38.p7 | 19:49556808 | CGTGGTCCCTGTGCG[-/T]TGAGGAGGACGGTGG | 51070 |
rs534563668 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NOSIP | GRCh38.p7 | 19:49573184 | TGTTTGATCCAAGCA[A/C]CTGTGGCTTTGACCA | 51070 |
rs534594993 | in-del | -/AT | | | intron-variant | NOSIP | GRCh38.p7 | 19:49572678 | GAGATACTTTAAAAT[-/AT]ATATATATATATGGC | 51070 |
rs534613832 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580035 | AACCCCGAAAGGGAA[C/G]GGGCTGTCAAAAAGG | 51070 |
rs534661672 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564967 | TCAAAAACTCACAAA[C/G]TAATTACTACACCAG | 51070 |
rs534685197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49573882 | TTTTTTTTTTGGAGA[C/T]GGAGTCTCACTCTGT | 51070 |
rs534748674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49566271 | GTGATCCGCCCACCT[C/T]GGCTTCCCAAAGTGC | 51070 |
rs534854577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578509 | TGGCATGAGGAAACA[A/G]GTAAAATGAGGCCGG | 51070 |
rs535351142 | snp | A/G | 3.80793e-05 | 0.00436328 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555694 | GCGCCCACGCCGCGA[A/G]TGAAGGCGCCACGTC | 51070 |
rs535367092 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564466 | CTCAAAAAAAAAAAA[A/C]AAAAAAAAAACAAAA | 51070 |
rs535373639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49563433 | TCCTGGCCTCCCAAA[A/G]TGTTGGGATTACAGG | 51070 |
rs535410051 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49556026 | GGTAGAGAGTGGCAG[G/T]GGAGGAGCCTTGGGA | 51070 |
rs535430320 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49581422 | CTTTCACAGCTGGCT[C/G]TAGCTGGCCAAGGAG | 51070 |
rs535554454 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49568793 | CTAAAAAAAAAAAAA[A/T]AATAGTTTGTTTGTT | 51070 |
rs535657832 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575996 | CAAAATTAGCCGGGC[A/G]TGGTGGCGGGCGCCT | 51070 |
rs535685725 | snp | C/G/T | 8.63602e-05 | 0.00657067 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49557151 | CCGGCTCACGATAGC[C/G/T]GACTCCTTCTCCAGG | 51070 |
rs535824161 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49560189 | AGCCGCTGCCTGTGT[G/T]CTGGGGCCACGGGCT | 51070 |
rs535929213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NOSIP | GRCh38.p7 | 19:49576828 | GGCGAAGGTCGTGAT[A/G]AGCCAAGATCGCACC | 51070 |
rs536154229 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575292 | GCATGAGCCACCATG[C/T]GCAGCCTCCTCCTAT | 51070 |
rs536334860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49561052 | ACCAAGGGGGCCACT[A/G]TTGTTGATGAATCCA | 51070 |
rs536428893 | in-del | -/TGTT | 0.0023933 | 0.0345097 | intron-variant | NOSIP | GRCh38.p7 | 19:49562119 | AACAGCCTGCATGCC[-/TGTT]TGTTTGTTTGTTTTT | 51070 |
rs536696612 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NOSIP | GRCh38.p7 | 19:49558555 | TGAGCCACCACCCCC[A/G]ACCCATTTAGCATAT | 51070 |
rs536756566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49572937 | AAGATCGGGCCACTG[C/T]ACTCCAGCCTGGCCA | 51070 |
rs536887253 | in-del | -/A/AAA | 0.102014 | 0.201495 | intron-variant | NOSIP | GRCh38.p7 | 19:49559510 | TGAAGACTCTGTCTC[-/A/AAA]AAAAAAAAAAAAGAA | 51070 |
rs537021503 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49571129 | TAACAGGCGCCCACG[C/T]CCAGCTAATTTTTTT | 51070 |
rs537142842 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579892 | ATTTTCGTAAGAAAA[C/T]ATTAACATCAAACTG | 51070 |
rs537146524 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49572050 | AATCCAGAATGTATT[C/T]TACTCTTTCAGCACA | 51070 |
rs537209616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49557597 | ATGGAGAGCCTCACC[C/T]GGCACTCAGCTAAGC | 51070 |
rs537347941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577739 | CACTGCACTCCAGCC[C/T]GGGTAACAGAGCAAG | 51070 |
rs537534103 | snp | C/T | 0.00139152 | 0.0263405 | missense | NOSIP | GRCh38.p7 | 19:49556355 | GGTCTGTGAGTTTGT[C/T]TCCAGTCACAGGGTC | 51070 |
rs537759894 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49570461 | TTTACAGTTGGATGC[A/G]ATCTGACAAATGTAT | 51070 |
rs537813373 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49573275 | CAGACAGCTAGTGTG[C/T]GTCTTGTCCTCCCCT | 51070 |
rs537960946 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOSIP | GRCh38.p7 | 19:49567982 | CACACCCAACCAACA[A/G]GGGACTAATATGTAG | 51070 |
rs537993424 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49578673 | TTTTTTTGAGACAGA[A/G]TCTCACTCTGTCGCC | 51070 |
rs538015674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49568623 | TCCAGCAAATCAAGA[A/G]GAAAATTACAGCCAC | 51070 |
rs538235510 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49558173 | GTCCTCTGATTTGGC[C/T]GTCAGCCCGTTTTAC | 51070 |
rs538343901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576011 | GTGGTGGCGGGCGCC[C/T]GTAGTCCCAGCTACT | 51070 |
rs538554384 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580761 | GGAATATGGGGAACG[C/T]TTACTATGTACGAGG | 51070 |
rs538563025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49574016 | AAGCACACACCACCA[C/T]GCCTAGATACTTTTT | 51070 |
rs538598650 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49574775 | TTGGAGTGCAGCGGC[A/G]GATCTCGCCTCCCAG | 51070 |
rs538608316 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49566315 | GTGAGCCACTGCGCC[C/T]GGCCTTTTCTTTAAG | 51070 |
rs538729933 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOSIP | GRCh38.p7 | 19:49559393 | GTGGTAGTGCACACC[C/T]GTGGTTCCAGCTACT | 51070 |
rs538769686 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOSIP | GRCh38.p7 | 19:49560130 | AGGCACAGAGACAAC[A/G]CGGTGGTGGGGGTGG | 51070 |
rs538824019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49571940 | CAGTGAGCCCAGATC[A/G]CACCACTGCACTTCA | 51070 |
rs538842947 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49562601 | CAAAGAAGTTGATGG[C/T]CAGGTGCAGTGGCTG | 51070 |
rs538927162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565105 | ACATAGCAAAACCTT[A/G]TCACTACAAAACATA | 51070 |
rs538978638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49557887 | AGTGATGGATGCTCA[C/T]GAGGGCCTCCGACAT | 51070 |
rs538989001 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565605 | AAATATATATATATA[A/T]AAATTTGCTGGGTGT | 51070 |
rs539145435 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577990 | TGCTAATGAGTACCA[C/G]GGTTTCTTTTTGGGT | 51070 |
rs539202983 | snp | A/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565985 | ACGTGTCCAAGGATG[A/T]TTTTCAGATAAATTC | 51070 |
rs539285884 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49561546 | ACCCTTTTAAATGAC[C/T]TTATTGAGACACAAT | 51070 |
rs539590423 | snp | A/G | 9.63623e-05 | 0.0069406 | intron-variant | NOSIP | GRCh38.p7 | 19:49556268 | AGGGGGTGAAGGGGA[A/G]GGGCGGGGCCTTGGA | 51070 |
rs539612426 | snp | A/C | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578260 | TCCTGAGTAGCTGGG[A/C]TTATAGGTGCCAGCC | 51070 |
rs539776329 | snp | A/T | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580410 | TAATGATTGACAGGG[A/T]ATCGGGAATCCAAAA | 51070 |
rs539811953 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSIP | GRCh38.p7 | 19:49569556 | TCACACCTGTAATCC[C/T]AGCACTTTAGGAGGC | 51070 |
rs539907057 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49582134 | TAATCTCAACTACCC[A/G]GGAGGCTGAGTCAGG | 51070 |
rs539920923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49562986 | ACAGTTGCAAAGGAT[A/G]CAATTTCCAGCAACG | 51070 |
rs540006660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49567215 | GCAAGCTCCACCTCC[C/T]GGGTTCACGCCATTC | 51070 |
rs540179853 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | NOSIP | GRCh38.p7 | 19:49564163 | AACGCACATTAAAAC[C/T]TCACTGAAGGCCGAG | 51070 |
rs540261779 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49573547 | AGAATCAATGAACCA[A/C]CTCCAATCCTAGGGC | 51070 |
rs540322853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49574176 | CTTGCTCATTTAATA[A/G]GTAGGAAAATTGAAG | 51070 |
rs540587697 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580332 | CTGCCCGATGGACGG[G/T]TGGCCACCTCCAGCA | 51070 |
rs541008645 | snp | C/T | | | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49582456 | ATTTTTGTATGACTC[C/T]TGTGAAAAGTAAAAT | 51070 |
rs541324168 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49571582 | TCACAGCATGTCCCA[C/G]CTGGGAAATGGCAGA | 51070 |
rs541339960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49563851 | GCAAGAAATAAAAAA[C/T]ATGGATAGGAAATCC | 51070 |
rs541512816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577279 | ATACATCCATGCAGG[C/T]GGGGCGCGGTGGCTC | 51070 |
rs541526885 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49569773 | AGATCGCGCCATCGC[A/G]CTCCAGCCTGGGGGA | 51070 |
rs541578743 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSIP | GRCh38.p7 | 19:49563244 | GCAGTGGTACAATCA[C/T]AGCTCACTGCAGCCT | 51070 |
rs541598736 | snp | C/T | 0.00318978 | 0.0398085 | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555419 | GCGCACCACCATGCC[C/T]GGCTAATTTTTGTAT | 51070 |
rs541621388 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555469 | TCACCATGTTGGCCA[A/G]GCTGGTCTCGAACTC | 51070 |
rs541669040 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49569281 | TCACTGCAAGCTCCA[C/T]CTCCCAGGTTCACAC | 51070 |
rs541708409 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49555895 | CTCCAGGTGGTAGTG[G/T]GGATTCCTAAGCGGG | 51070 |
rs541728959 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564944 | GTATGATCCCATTCA[C/T]GTGACGTTCAAAAAC | 51070 |
rs541995835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49561963 | CTAGGGGTTTGATCA[C/T]TTTAACTTTTACTTT | 51070 |
rs542161485 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575894 | CCCAGCACTTTGGGA[A/G]GCCAAGGCGGGCAGA | 51070 |
rs542449069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49574151 | ACAGGCATGAGCTAC[C/T]GCGCCCAGTCTTGCT | 51070 |
rs542466981 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49582068 | AACATGGTGAAACCC[A/C]ATCTCTACTAAAAAT | 51070 |
rs542639743 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579486 | CAGTTTTAGCCCACC[C/T]GATAAAGGAAGTCCC | 51070 |
rs542701043 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580257 | CTCAGGAGAACTGGC[C/T]GATGCTAGCTACCAC | 51070 |
rs542757741 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49581174 | GGGAGGGAGGAGGAG[G/T]GTCGAATCTAATCCC | 51070 |
rs542764441 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NOSIP | GRCh38.p7 | 19:49557911 | CCGACATGACCACCA[A/G]GCTGTGTGGAGGACA | 51070 |
rs542920248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49559456 | CTGGGATATCAGTGA[A/G]CCAAGATGTCCCCAT | 51070 |
rs543052467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49568736 | GATTGCTTAAGGCCA[A/G]GAGTTCAAGACCAGC | 51070 |
rs543494536 | snp | A/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49571907 | GAAGAATCGCTTGAA[A/C]CCAGGAGGTGGAGGT | 51070 |
rs543640534 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49559580 | GTCTTCTACAAAATA[C/T]ACCACTAATTGAGCA | 51070 |
rs543723946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49570823 | TCAACTCCCTTGACC[C/T]TCTGCAGTATTTGGC | 51070 |
rs543762601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49578685 | AGAGTCTCACTCTGT[C/T]GCCCAGGCTAGAGTG | 51070 |
rs543931497 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575897 | AGCACTTTGGGAGGC[C/G]AAGGCGGGCAGATCG | 51070 |
rs544052971 | snp | A/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49567225 | CCTCCCGGGTTCACG[A/C]CATTCTCCTGCCTCA | 51070 |
rs544137457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49563127 | TTGAACTTGTATTTC[C/T]GTTCCACTTCCCTCT | 51070 |
rs544315661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49560449 | AGAGAACACAGTGCC[A/G]GGCCACATGGGGTCA | 51070 |
rs544534025 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49568905 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 51070 |
rs544570498 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575200 | GACAGAGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 51070 |
rs544627616 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575021 | GCGCCCGCCACCATG[A/C]CCGGCTAATTTTTTT | 51070 |
rs544641789 | snp | A/G | | | synonymous-codon | NOSIP | GRCh38.p7 | 19:49556700 | GGTCCGACATGCGCA[A/G]GGGCTTCCCTGACAT | 51070 |
rs544881259 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49581112 | ATATTAATTTTTCTA[A/G]CTCGGACAGACGAAC | 51070 |
rs544941429 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49582010 | TTTGGGAGGCCGAGG[C/T]GGGTGGATCACTTGA | 51070 |
rs545166856 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564471 | AAAAAAAAAAAAAAA[A/C]AAAAACAAAATAAAA | 51070 |
rs545190493 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579439 | CTTCTGAGATATCAG[C/G]AGAGAGATAATAGCC | 51070 |
rs545284931 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49573257 | TGAACTCTGGGAGTG[G/T]ATCAGACAGCTAGTG | 51070 |
rs545442649 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49578865 | CCTGATCTCATGATC[C/T]GCCCGCCTTGGCCTC | 51070 |
rs545488538 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49570701 | GTGAACGTCCAACAC[C/G]TGTTGCCTCCCCTCA | 51070 |
rs545540288 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49556495 | CTGGCCCCAAAGCCG[C/G]ACCGCCCCGCAGGTT | 51070 |
rs545621588 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | NOSIP | GRCh38.p7 | 19:49563585 | TACAACCTCCGCCTC[-/T]TGGGTTCAAGCAATT | 51070 |
rs545649258 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NOSIP | GRCh38.p7 | 19:49572303 | GTAGAGATGGGGTTT[C/T]GCCATGTTGGGCAGG | 51070 |
rs546026022 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49574963 | TGCCTCCAGGGTTCA[C/T]GCCATTCTCCTGCCT | 51070 |
rs546100141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577301 | CGGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT | 51070 |
rs546260512 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580725 | GTAGCTAATCGAAAG[C/T]TCCGGATATTGAAAC | 51070 |
rs546288056 | in-del | -/CTGCTGCCAT | 0.00119737 | 0.0244387 | intron-variant | NOSIP | GRCh38.p7 | 19:49571464 | AAACTACAAAGCAGA[-/CTGCTGCCAT]CTGCTGCCATCTGCT | 51070 |
rs546369747 | snp | C/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49560783 | GAGCTGATCTGCCCC[C/G]CTTGATGGGAAAGCG | 51070 |
rs546407959 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575798 | TAATTGTCATAGGTC[A/C]CCAAATTCATTCTTT | 51070 |
rs546513223 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49568190 | TCACACGGGCTAGGT[A/C/G]GTTAAGACATACCAA | 51070 |
rs546619394 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565595 | CTCTACAAAAAAATA[A/T]ATATATATAAAAATT | 51070 |
rs546674882 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | NOSIP | GRCh38.p7 | 19:49574645 | GGCTACCAGCATTGT[A/G]GGGTTCTGGTGACAC | 51070 |
rs546679072 | snp | A/G | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579431 | TATCTGATCTTCTGA[A/G]ATATCAGGAGAGAGA | 51070 |
rs546737851 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49566938 | CTCCTGCCTCAGCCT[A/C]CTGAGTAGCTGGGAT | 51070 |
rs546759345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49558307 | AGGCTGAAGTGCAGC[A/G]GTGCCATCTCAGCTC | 51070 |
rs546847506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49571899 | CTGAGGCAGAAGAAT[C/T]GCTTGAACCCAGGAG | 51070 |
rs546906822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49572794 | GCCTGGCCAATGTGG[C/T]GAAACCCTGTCTCTA | 51070 |
rs546924582 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49579124 | AGAGATGTAAAAGAC[A/G]ATAGCAATTACTTAA | 51070 |
rs547090881 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49559099 | CAATTATTTGCTAGA[A/T]TTCACAGAACTCAGC | 51070 |
rs547227113 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579690 | CACGAATAAATGCCA[A/G]TTAAGATCTTCTCAC | 51070 |
rs547367674 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NOSIP | GRCh38.p7 | 19:49564170 | ATTAAAACTTCACTG[A/C]AGGCCGAGCACCGTG | 51070 |
rs547439747 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555543 | GGATTACAGGCGTGA[A/G]CCACCGTGCCTGGCC | 51070 |
rs547599009 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NOSIP | GRCh38.p7 | 19:49563505 | AAAATTCTTTTTTTT[G/T]TTTTTGAGATCGAGT | 51070 |
rs547635548 | snp | G/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555567 | CCTGGCCAGATTTTG[G/T]TCTTAATGTGAGACC | 51070 |
rs547640814 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49570970 | GGGAGCATTTAAACT[C/T]TTTTTAATTTAATTT | 51070 |
rs547671187 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577426 | GCTAGGCGTGGTAGC[A/C/G]CATGCCTGTAGCCCC | 51070 |
rs547866314 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577505 | AGATCACGCCACTGC[A/T]CTCCAGCCTGGGTGA | 51070 |
rs547873131 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49569069 | GCCTCCCAGAGTGCT[A/G]GGATTACAGGTGTGA | 51070 |
rs548024117 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49582419 | AGTTGGGATTACAGG[C/G]GCCCACAACCACGCC | 51070 |
rs548034329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575360 | TTTCACCTTAATTAT[C/T]TCCACAAAGGCCCTA | 51070 |
rs548097426 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575927 | GTGAGGTCAGGAGAT[G/T]GAGACCATCCTGACT | 51070 |
rs548204036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49567835 | TGCCACCAGGCCCGG[C/T]TAATTTTTTTGCATT | 51070 |
rs548251020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49561711 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 51070 |
rs548393022 | snp | A/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49569938 | TCAACATGGTAAAAC[A/C]CTGTCTCTACCAAAA | 51070 |
rs548425632 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49574812 | GTGAATCTCCTGCTT[C/T]AGCCTCCTAAGTAGC | 51070 |
rs548467293 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | NOSIP | GRCh38.p7 | 19:49574192 | GTAGGAAAATTGAAG[C/G]TTGGAGAAATTGGCC | 51070 |
rs548526705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49566242 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT | 51070 |
rs548585453 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | NOSIP | GRCh38.p7 | 19:49559260 | AGAGCTGCAGGGAAA[C/G]TGCTTCATTCTCTCA | 51070 |
rs548662653 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49566052 | TTTGAGACAGTCTCG[-/CT]CTGTCGTCCAGGCTG | 51070 |
rs548827694 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49574537 | CTGCCACCTGTCTCA[C/G]TCTGCTCCAGCTGCC | 51070 |
rs548885685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49559880 | ACACAGCCTCCTCCT[A/G]GCGGTTCCCTTGCTC | 51070 |
rs549050157 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | PRRG2, NOSIP | GRCh38.p7 | 19:49580623 | CGCCCAGCAGAAGGC[A/G]CCGGAAGTAGAGCTG | 51070 |
rs549136921 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49571669 | CAACTGTCAGTTTTC[C/G]TAGGAAAGTCACAAT | 51070 |
rs549216099 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578430 | TGCCTGCCCAATGGG[G/T]ATTTTTAAAACAGGT | 51070 |
rs549458270 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565568 | AGTCTGGGCAACATA[C/T]TGAGACCCCATCTCT | 51070 |
rs549501439 | snp | G/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49567528 | CAACTTTGCCCCAGG[G/T]CTTCCTGGGACTGGC | 51070 |
rs549523171 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49557672 | TGCATGCCCCAGCCC[A/G]TGTTTGGGACGGGGG | 51070 |
rs549659448 | snp | C/G | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579869 | CTCACTTTTATATAA[C/G]TTTGAACATTTTCGT | 51070 |
rs549973669 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | NOSIP | GRCh38.p7 | 19:49569370 | AGCTAATTTTTTTTA[A/T]TTTTTTTTTAGTAGA | 51070 |
rs550145869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49582205 | GAGATAGCGCCACTG[C/T]ACTCCAGCCTGGGTG | 51070 |
rs550234533 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576126 | AGCGACAGAGCGAGA[C/T]TCCATCTTATAAAAA | 51070 |
rs550313534 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | NOSIP | GRCh38.p7 | 19:49576770 | ATACCTGTAATCCCA[A/G]CTACTCGGGAGGCTG | 51070 |
rs550413375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49581805 | GGGAAAGAAAGATAA[A/G]CTGCCTGCTCCTTGC | 51070 |
rs550436307 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49561584 | CCATAAAATTAACCC[A/T]TTTAAAGTGGTTTCA | 51070 |
rs550471947 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555072 | ATCACACTGCAGCCC[A/G]GAAGACACGTTCCTG | 51070 |
rs550599549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575115 | TGATCTGCCCACCTC[A/G]GCCTCCCAAAGTGCT | 51070 |
rs550600095 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49559210 | GCAGAATCTAGTAGA[C/G]ACTAGATTTGAGCTT | 51070 |
rs550613133 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSIP | GRCh38.p7 | 19:49567471 | TCCATACAGACTGCA[C/T]AGGTCTATATACCTC | 51070 |
rs550638826 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49559710 | GCAATGCTCTGAGAG[A/C]CCTACACCCCATTAG | 51070 |
rs550695690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49560769 | CTCTGCAGCCCTCAG[A/G]GCTGATCTGCCCCCC | 51070 |
rs550765873 | snp | A/C | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564468 | CAAAAAAAAAAAAAA[A/C]AAAAAAAACAAAATA | 51070 |
rs550942833 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSIP | GRCh38.p7 | 19:49572916 | GGGCAGAGGTTGCAG[C/T]GAGCCAAGATCGGGC | 51070 |
rs551205113 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580447 | CCCAGTCTCCCTCAA[A/G]ACCCCAGGCCTCTAG | 51070 |
rs551215360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49573641 | ATAATTCATTAGTAA[C/T]ATGTGAATCACAGAA | 51070 |
rs551533402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578324 | AGATGAGGTTTTACC[A/G]TGTTGGCCAGGCTGG | 51070 |
rs551542286 | snp | A/C | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580453 | CTCCCTCAAGACCCC[A/C]GGCCTCTAGCCCGCA | 51070 |
rs551545032 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOSIP | GRCh38.p7 | 19:49571113 | TCCCAAGTAGCTGAG[A/G]TAACAGGCGCCCACG | 51070 |
rs551642728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49556817 | CTGTGCGTGAGGAGG[A/G]CGGTGGGGAACCCTG | 51070 |
rs551679270 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49557530 | ACAGCCTAACAGTGG[A/T]TACCCACCTCAGCGG | 51070 |
rs551739793 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577628 | AGCTGGCTGGGCGCC[G/T]ATGGCTCACACCTGT | 51070 |
rs551788581 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NOSIP | GRCh38.p7 | 19:49562532 | CTGTTGAGCCCAGGA[A/G]ATGGAGATGAGCCTA | 51070 |
rs551850057 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49563329 | TACAGGCATGTGCCA[A/C]CACGCCCAGCTAATT | 51070 |
rs551927374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564326 | GGTCGTGGTGGTGTG[C/T]GCCTGTAATCCCAGC | 51070 |
rs552074359 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NOSIP | GRCh38.p7 | 19:49569230 | TTGAGACGTTATCTC[A/G]CTCTTTCACCCAGGC | 51070 |
rs552144592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576714 | ACATGGAGAAACCCC[A/G]TCTCTACTAAAAATA | 51070 |
rs552246672 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555016 | TCCTAGTCCGGGTGC[G/T]GCGCACTTTTTCACA | 51070 |
rs552393462 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575970 | CCCCGTCTCTACTAA[A/T]AATACAAAAACAAAA | 51070 |
rs552416093 | in-del | -/G | 0.0123036 | 0.0774623 | intron-variant | NOSIP | GRCh38.p7 | 19:49569367 | CCAGCTAATTTTTTT[-/G]TATTTTTTTTTTAGT | 51070 |
rs552475202 | in-del | -/TTTTTTTGCATTT | 0.00358779 | 0.0422022 | intron-variant | NOSIP | GRCh38.p7 | 19:49567839 | ACCAGGCCCGGCTAA[-/TTTTTTTGCATTT]TTTTTTTAGTAGAGA | 51070 |
rs552513559 | in-del | -/T | 0.0123036 | 0.0774623 | intron-variant | NOSIP | GRCh38.p7 | 19:49569370 | AGCTAATTTTTTTTA[-/T]TTTTTTTTTAGTAGA | 51070 |
rs552759917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49558766 | TGAGAAGGATTTGGC[C/T]GGAAGCAGGGGAGGG | 51070 |
rs553036907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49559327 | TTCGAGACCAGCCTG[A/G]GCAACAAAGTGAGCT | 51070 |
rs553039478 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49581347 | CAGAAACGGGGATCA[C/G]GCCTGGTTACCGGGA | 51070 |
rs553050416 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565850 | CAGCCCACCAGGCAC[A/G]TCCTTGGTCTTTATG | 51070 |
rs553050734 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | NOSIP | GRCh38.p7 | 19:49573883 | TTTTTTTTTGGAGAC[A/G]GAGTCTCACTCTGTC | 51070 |
rs553194756 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49571333 | AAGATCCTGAGACCA[C/G]AAAGCGTGAGCGCCT | 51070 |
rs553270459 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564992 | CACCAGAAGTTATGT[G/T]TGGGTGGGTGTGGTG | 51070 |
rs553374373 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49557793 | GCTCAGCCCTGCCTG[C/G]CGCACAGCAGTTGCC | 51070 |
rs553396014 | snp | A/G | 2.72572e-05 | 0.0036916 | intron-variant | NOSIP | GRCh38.p7 | 19:49557074 | CCCAACCCACAAGAA[A/G]CCCAACCTGAGTCAC | 51070 |
rs553515304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578523 | AAGTAAAATGAGGCC[A/G]GGCTCAATGGCTCAC | 51070 |
rs553629696 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49559240 | TCCAGCTGTCCTCTC[C/T]CAATAGAGCTGCAGG | 51070 |
rs553728144 | snp | A/C/G/T | 0.000144131 | 0.00848809 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555706 | CGAATGAAGGCGCCA[A/C/G/T]GTCGTTGCGCACCCA | 51070 |
rs553777938 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49581465 | GAGGAAGGGGCAGTG[C/T]TCACATTTCTGGGCA | 51070 |
rs553992874 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49562852 | ACCACTACACTCCAG[C/G]CTGGTGACAGACAGA | 51070 |
rs554194849 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49562221 | CTGCCTCCCAAGTTA[A/C]AGCGATTCTCCTGCC | 51070 |
rs554475351 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575747 | GGCTGTGTTCCAATA[A/C]AACTTTACTTTTAGA | 51070 |
rs554605837 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49568548 | TGATATATCAACTGC[A/G]TTGGAATAAATTCAC | 51070 |
rs554611053 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580918 | TTTTCTTGCTGCATC[G/T]TAAAACAATTGAGAA | 51070 |
rs554803903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49567183 | GCTGGAGTGCAGTGG[C/T]GCGATCTCGGCTCAC | 51070 |
rs554856886 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOSIP | GRCh38.p7 | 19:49560287 | TGGTGGAGGGGCTGA[C/T]GGCTGACTCCCCTCC | 51070 |
rs554955782 | in-del | -/T | 0.0130921 | 0.0798413 | intron-variant | NOSIP | GRCh38.p7 | 19:49569602 | ACTTGAGGTCAGGAG[-/T]TTTGAGACCAGCCTG | 51070 |
rs555123388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565202 | ACCTGAGCCCAGGGA[A/G]GTCAAGGCTGCAGTG | 51070 |
rs555383743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NOSIP, PRRG2 | GRCh38.p7 | 19:49579218 | AGTAGTCTAGAATTA[C/T]GGTTGTTCTTTTAAA | 51070 |
rs555455108 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565731 | CCACTGCTCTCCAGC[A/C]TGGGCAATAGAGTGA | 51070 |
rs555667236 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49578731 | GGCTCACTGCAAGCT[C/G]TGCCTCCCGGGTTCA | 51070 |
rs555735689 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSIP | GRCh38.p7 | 19:49570492 | ACACCCTTGTGACCA[C/T]GACCCTATGGAGATA | 51070 |
rs555751419 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49562480 | CTCAGGGCTCACGCC[C/T]GTAATCCCAAAACTT | 51070 |
rs555759446 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564420 | GATCACGCCACGGCA[C/G]TCTAGCCTAGGGGAC | 51070 |
rs555844856 | snp | A/G | 8.49842e-05 | 0.00651804 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49556401 | AATCAGCTTCTCCAC[A/G]CATTCGAGGGTGACC | 51070 |
rs555883614 | snp | C/T | 5.81897e-05 | 0.00539365 | missense | NOSIP | GRCh38.p7 | 19:49556940 | AGAAGCTGGGCAGCA[C/T]TTTGTCCTTGTCCTT | 51070 |
rs555908707 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49573408 | CCCTGAGCTACCTCC[A/G]TTACAGCCCGTCCCT | 51070 |
rs555966804 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | NOSIP | GRCh38.p7 | 19:49561900 | AAAAAAAAAAAAAAA[A/T]GACATTGCCTAAGCC | 51070 |
rs556026189 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555357 | TCCGCCTCCTGGGTT[C/G]AAGCGATTCTCCTGC | 51070 |
rs556250350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49561183 | TGACACTTAGCTAAG[A/G]CTTGACCCAATCGCT | 51070 |
rs556335833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576091 | AGTGAGCGGAGATCA[C/T]GCCACTGCACTCCAG | 51070 |
rs556382589 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49570239 | CAGAAGTTGGGGTGG[A/G]GAGCACAACCAAGGG | 51070 |
rs556539069 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49557626 | GCATTTAATTAATGT[C/T]ACCTGCTGGCCAATT | 51070 |
rs556572548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49568022 | TTCTACTATAAGGCA[C/T]GCATTCATAGAAATC | 51070 |
rs556691373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49559324 | GAGTTCGAGACCAGC[C/T]TGGGCAACAAAGTGA | 51070 |
rs556715159 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580181 | ACCCCCAGCAATCCC[A/C]GTCCACTCCTTCCCT | 51070 |
rs556742907 | snp | A/G/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49563742 | TCAGGTGATCCACCC[A/G/T]CCTCGGCCTCCCAAA | 51070 |
rs556776512 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580763 | AATATGGGGAACGCT[G/T]ACTATGTACGAGGCA | 51070 |
rs556914694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49573359 | GAAGCCTGCCTCTCC[A/G]GGATCAGTTAGGTTC | 51070 |
rs557119869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564497 | TAAAACTTCATTGAG[A/G]TACCTCCCCACACGC | 51070 |
rs557181130 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565142 | TTAGCTGGGCATGGT[G/T]GTGCATGCCTGTAGT | 51070 |
rs557195535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49557897 | GCTCATGAGGGCCTC[C/T]GACATGACCACCAGG | 51070 |
rs557478722 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578588 | AGGCAGGAGGATCGC[A/T]TAAGCCCAGGAGTTT | 51070 |
rs557517926 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49571954 | CGCACCACTGCACTT[C/T]AGCCTGGCGACAGAG | 51070 |
rs557554204 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49566025 | TTCTTTCTTTTCTTC[C/T]TCTTTTTTTTTTTTG | 51070 |
rs557692802 | snp | A/C | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578491 | ACATAATTAGCTGAT[A/C]CCTGGCATGAGGAAA | 51070 |
rs557718425 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49558501 | TGACCTCAAGTGATC[C/T]GCCTGCCTCGGCCTC | 51070 |
rs557807129 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NOSIP, PRRG2 | GRCh38.p7 | 19:49579190 | GGACTTGACTCTGCA[A/C]CACGTAATGGATAGT | 51070 |
rs557974024 | snp | G/T | 5.0755e-05 | 0.00503735 | intron-variant | NOSIP | GRCh38.p7 | 19:49556293 | CTTGGAGTGCTGGGG[G/T]AAGGGGAGGGGTGGG | 51070 |
rs558231718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49563007 | TCCAGCAACGTAAAT[A/G]TGTAGCTGATGGAAT | 51070 |
rs558310552 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555278 | TTTTTTTCTTCTTTG[A/T]GATGGAGTCTCGCTC | 51070 |
rs558340195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576443 | TTAGCCGGGCATAGT[A/G]GCATGCGCCTGTGGT | 51070 |
rs558425234 | in-del | -/A | | | intron-variant | NOSIP | GRCh38.p7 | 19:49561884 | GCTCTGTCACAATTA[-/A]AAAAAAAAAAAAAAA | 51070 |
rs558853020 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578323 | GAGATGAGGTTTTAC[C/T]ATGTTGGCCAGGCTG | 51070 |
rs558921247 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49581988 | CTCACACCTGTAATC[C/G]CAGCACTTTGGGAGG | 51070 |
rs558982818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575011 | GGGACTACAGGCGCC[C/T]GCCACCATGCCCGGC | 51070 |
rs559011828 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49561619 | AGGTGTAGTGGCTCA[C/T]GCCTGTAATCTCAGC | 51070 |
rs559135116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49563781 | ATTACAGGTGTGAGC[C/T]ACTGTGCCCAGCCTG | 51070 |
rs559157704 | in-del | -/A | 0.286564 | 0.247312 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565272 | GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAAGTC | 51070 |
rs559374808 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565332 | TGACTAGGAGGGGCA[C/T]AGGTAGCATCTGGGA | 51070 |
rs559429819 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49582508 | GCTCACGCCTGTAAT[C/G]CCAGCACCAGCACTT | 51070 |
rs559456339 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555521 | GCCTCGGCCTCCGAA[A/G]GTGCTGGGATTACAG | 51070 |
rs559498056 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49578824 | GCTAAGGGGTTTCAC[A/C]GTGTTAGCCAGGATG | 51070 |
rs559514289 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49573768 | ATGACAACCTCCCCA[C/T]GTTCTGCCCATTTAT | 51070 |
rs559598820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49571585 | CAGCATGTCCCAGCT[A/G]GGAAATGGCAGAGCT | 51070 |
rs559627386 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578298 | CCAGCCAATTTTTGT[A/C]TTTTTAGTAGAGATG | 51070 |
rs559656556 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49572232 | TGCCTCAGCCTTCCA[C/G]GTAGCTGGGATTACA | 51070 |
rs559658425 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564819 | GGCCATATCACATAA[C/T]GGAAACACCCAGCAA | 51070 |
rs559712229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576651 | GCACTTTGGGAGGCC[A/G]AGGTGGGCGGATCAC | 51070 |
rs559725529 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49555908 | TGGGGATTCCTAAGC[C/G]GGTCAAGGTGAAGCG | 51070 |
rs559725758 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49569084 | GGGATTACAGGTGTG[A/C]GCCCACTGCGCCCGG | 51070 |
rs559788582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49569797 | TGGGGGACAAGAGTG[A/G]GACTTTGTCTCAAAA | 51070 |
rs560163953 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49562440 | CTGCAGGCTTTTTTA[A/T]CCCTTAAAATGATTT | 51070 |
rs560191336 | in-del | -/T | 0.323197 | 0.239044 | intron-variant | NOSIP | GRCh38.p7 | 19:49573858 | ACCAGGACTGAAGTA[-/T]TTTTTTTTTTTTTTT | 51070 |
rs560315596 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOSIP | GRCh38.p7 | 19:49561274 | CAGAGGGCAGGTCAG[A/G]GTAGGGCTCTGTGTC | 51070 |
rs560414930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576434 | TTTAAAAAATTAGCC[A/G]GGCATAGTGGCATGC | 51070 |
rs560485711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49568122 | CCTCGTAAACTTTGT[C/T]GGTGATGCTTAAAGA | 51070 |
rs560509221 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565434 | GACAGTTATGCTTTC[C/T]GTACTTCTCTGTACA | 51070 |
rs560531956 | snp | A/G | 9.25626e-05 | 0.00680241 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49560665 | GTAGACGGCCCCTGC[A/G]GTGCAGTTCTTGCCA | 51070 |
rs560737588 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49567410 | ACAGGCGTGAGCCAC[C/T]GTGCCCGGCCCCAAA | 51070 |
rs560955689 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580285 | CACTTGACTGAGTTT[A/G]TAGTGAGAGAGAGAG | 51070 |
rs560969411 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49564038 | ATTTGCCTTTCTGAT[C/T]CTCATTCTCTCACAA | 51070 |
rs560990784 | snp | A/C | | | intron-variant | NOSIP | GRCh38.p7 | 19:49560427 | AGTGAGTTCATGCGC[A/C]GAAGGCAGAGAACAC | 51070 |
rs561013810 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49573416 | TACCTCCGTTACAGC[A/C]CGTCCCTCGGTATTT | 51070 |
rs561117451 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565971 | ACCCAATGTCTAGCA[C/T]GTGTCCAAGGATGTT | 51070 |
rs561194068 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565580 | ATATTGAGACCCCAT[C/G]TCTACAAAAAAATAT | 51070 |
rs561290897 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565593 | ATCTCTACAAAAAAA[-/T]ATATATATATAAAAA | 51070 |
rs561332523 | snp | A/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49569422 | CCAGGATGGTCTTGA[A/T]CTCCTGACCTCGTGA | 51070 |
rs561416894 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49557393 | GTAACTGCCACCCTG[C/G]GTGGGTGTGAACCTT | 51070 |
rs561506895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, splice-donor-variant | NOSIP | GRCh38.p7 | 19:49564154 | CACCAGGGAAACGCA[C/T]ATTAAAACTTCACTG | 51070 |
rs561596287 | snp | C/G | | | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49582362 | CTCACTGCAACCTCT[C/G]TCTCCCCTTTCAAGT | 51070 |
rs561705860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49571525 | AAGAGCAGGAGCGAC[C/T]GATGTCAGCATAATC | 51070 |
rs561803435 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49570867 | GCTTTCCCAGAGATG[A/T]GCTTGCTTGCTGTTT | 51070 |
rs561826638 | snp | C/T | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579981 | TCCATGACTGCCTGA[C/T]CCCGAAGCTCCACAC | 51070 |
rs562120387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49569048 | CCTCGTGATCTGCCC[A/G]CCTTGGCCTCCCAGA | 51070 |
rs562185806 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NOSIP | GRCh38.p7 | 19:49562294 | GCCTGGCTAATTTTT[G/T]TGTATTTTTAGTAGA | 51070 |
rs562213174 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49576521 | GGTTGAGGCTGCAGT[C/G]AGTTATGATCGTGCC | 51070 |
rs562360537 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49563147 | CACTTCCCTCTCTGC[C/T]ACCCATTTTTAATCT | 51070 |
rs562377697 | snp | A/G | 0.000102611 | 0.00716207 | intron-variant | NOSIP | GRCh38.p7 | 19:49555846 | GGTAGAGAGAAGGAC[A/G]AGGTAGAGGCCGGCC | 51070 |
rs562570076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49568323 | TGGAAAGAGGGTTAT[C/T]TGAGATCTGATGGAA | 51070 |
rs562615128 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49560519 | AGTGTATATCGGGGG[A/C/T]GGGAGAGAGACAGGG | 51070 |
rs562878937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49566692 | GGCTGAGTGCAGCAA[C/T]GTTTACAACTAATTG | 51070 |
rs563026951 | snp | C/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49569093 | GGTGTGAGCCCACTG[C/T]GCCCGGCCTGGGAGG | 51070 |
rs563065693 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | PRRG2, NOSIP | GRCh38.p7 | 19:49580531 | TCACTAACGACTCCC[A/C]GTCCCTCGGTCGCTT | 51070 |
rs563079083 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49581113 | TATTAATTTTTCTAG[C/T]TCGGACAGACGAACT | 51070 |
rs563163551 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49574307 | TTCTTGGACATGACT[C/G]AAGACAAAAACCAAA | 51070 |
rs563165645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49571960 | ACTGCACTTCAGCCT[A/G]GCGACAGAGTGAGAC | 51070 |
rs563429552 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49559649 | GCCCTACCATCAGAG[A/G]TAGGTCATGGGAAGT | 51070 |
rs563596587 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49571649 | CATTCCTTTTAACTA[C/G]GTGACAACTGTCAGT | 51070 |
rs563776688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49563332 | AGGCATGTGCCACCA[C/T]GCCCAGCTAATTTTT | 51070 |
rs563804023 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSIP | GRCh38.p7 | 19:49572576 | TGCCACCATGCCCAG[C/T]TCATTTTTGTATTTT | 51070 |
rs564349495 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555487 | TGGTCTCGAACTCCT[A/G]ACCTCAAGTGATACG | 51070 |
rs564523585 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575816 | AAATTCATTCTTTTG[G/T]TTTTTTCCAGTTATG | 51070 |
rs564560762 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579466 | AGCCAAATCCCCAAA[C/T]AACCCAGTTTTAGCC | 51070 |
rs564720030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49561455 | TGTACCCATGTCCTG[C/T]GGTCCAGCAGCTGTC | 51070 |
rs564727577 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49559606 | GAGCACGTATTTAGT[C/G]CCTGGACTCAGCACC | 51070 |
rs564744454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49568874 | GTGGCGCAATCTCGG[C/T]TCACTGCAACCTCCG | 51070 |
rs564765771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49560424 | AGGAGTGAGTTCATG[C/T]GCAGAAGGCAGAGAA | 51070 |
rs564936577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49573575 | GGCCAGGGGAGGTGG[A/G]TTAGCAATGAACTAA | 51070 |
rs565278868 | snp | G/T | | | intron-variant | NOSIP | GRCh38.p7 | 19:49571839 | AAAATACAAAAATTA[G/T]CTGGGTGTGTTGGTG | 51070 |
rs565361585 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49579738 | TGTCTTTTGACAATC[C/T]TTAAGTGTCATGATG | 51070 |
rs565664417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578571 | AGCACTTTGGGAGGC[C/T]AAGGCAGGAGGATCG | 51070 |
rs565751129 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49556195 | GGGCGGCCTTACAGA[C/G]CAGAGAAGAAGGCGG | 51070 |
rs565879533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49563575 | CTCAGCTCACTACAA[C/T]CTCCGCCTCTTGGGT | 51070 |
rs565885266 | in-del | -/GA | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580289 | GACTGAGTTTATAGT[-/GA]GAGAGAGAGAGACAA | 51070 |
rs565992298 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577757 | GTAACAGAGCAAGGC[C/T]GTGTCTCGGGAAAAA | 51070 |
rs566103793 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49569552 | TGGCTCACACCTGTA[A/T]TCCCAGCACTTTAGG | 51070 |
rs566214205 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49570271 | CCCACCGATGTAAAA[A/C]GCAACTTCATCTCTA | 51070 |
rs566253568 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555583 | TCTTAATGTGAGACC[A/T]CATTCAATATGCTTA | 51070 |
rs566275307 | snp | A/C | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580896 | CTTTCCCAAATATAT[A/C]ATCCACTTTTCTTGC | 51070 |
rs566351638 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575479 | TGAATTTCACTACCC[A/C]TGAAAATGGGGCACC | 51070 |
rs566440835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49561120 | GACTGAGGCCAAGGC[A/G]TGGACCAGCCCAGTG | 51070 |
rs566465936 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575940 | ATTGAGACCATCCTG[A/G]CTAACACGGTGAAAC | 51070 |
rs566624929 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575913 | AAGGCGGGCAGATCG[C/T]GAGGTCAGGAGATTG | 51070 |
rs566764113 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49572741 | CACTTTGGGAGCCCA[A/G]GGCGGGCAGATCACC | 51070 |
rs566959771 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49566823 | CACACATACTATTTT[G/T]TTTTTTTTTTTGAGA | 51070 |
rs567002797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49581836 | TTTCTTCTCTGGCGG[A/G]CACTGCCTTCACTGA | 51070 |
rs567290356 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | PRRG2, NOSIP | GRCh38.p7 | 19:49580662 | TGCGGAAGTGCCTCG[C/T]CTGGCTTGCTCAAGT | 51070 |
rs567316144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49571883 | CCAGCTGCTCGGGAG[A/G]CTGAGGCAGAAGAAT | 51070 |
rs567402214 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NOSIP | GRCh38.p7 | 19:49573818 | TATGTATGTATGTAT[G/T]TATTTTGGAGACAGT | 51070 |
rs567539018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578455 | ACAGGTAGCTGGCAG[A/G]ATTTGAGTTTGGTCT | 51070 |
rs567548217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564447 | GGACAGAGCGAGACT[C/T]CATCTCAAAAAAAAA | 51070 |
rs567556755 | snp | C/T | 0.000134938 | 0.00821283 | synonymous-codon | NOSIP | GRCh38.p7 | 19:49557160 | GATAGCCGACTCCTT[C/T]TCCAGGAAGCCCCGC | 51070 |
rs567558545 | in-del | -/CTGA | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575937 | GAGATTGAGACCATC[-/CTGA]CTAACACGGTGAAAC | 51070 |
rs567601029 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | NOSIP | GRCh38.p7 | 19:49561025 | CATTTAATGGAGGGG[-/A]AAAAAAAAGACACCA | 51070 |
rs567653408 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP, PRRG2 | GRCh38.p7 | 19:49579094 | GAGTGGAAGGGGGAA[C/G]AGTTCTAAATTAAGA | 51070 |
rs567658934 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564964 | CGTTCAAAAACTCAC[A/T]AAGTAATTACTACAC | 51070 |
rs567673721 | snp | A/G | | | intron-variant | NOSIP | GRCh38.p7 | 19:49556137 | GGCCTAGGAGAGCGG[A/G]GGGGGGGAAGGGCGG | 51070 |
rs567692378 | snp | C/G | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565242 | TGGGCCACTGCACTC[C/G]AGCCTGGGAGTCAGA | 51070 |
rs567714099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49556012 | GGCGCAGAGAAGAGG[A/G]TAGAGAGTGGCAGGG | 51070 |
rs567970278 | snp | A/G | 8.08456e-05 | 0.00635738 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555687 | CCCCGGGGCGCCCAC[A/G]CCGCGAATGAAGGCG | 51070 |
rs568156507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49569433 | TTGATCTCCTGACCT[C/T]GTGATCTGCCCGCCT | 51070 |
rs568168516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49562702 | CCTGGCCAACATGGT[A/G]AAACCCTGTCTCTAC | 51070 |
rs568313266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49563421 | ACTCAAGTGAACTCC[C/T]GGCCTCCCAAAGTGT | 51070 |
rs568323517 | in-del | -/AT | | | intron-variant | NOSIP | GRCh38.p7 | 19:49573642 | TAATTCATTAGTAAC[-/AT]GTGAATCACAGAAGC | 51070 |
rs568409474 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49575504 | GGCACCCAGGCAGTA[C/T]GCAACATGAAGCGAC | 51070 |
rs568602303 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NOSIP | GRCh38.p7 | 19:49576808 | ACAATCACTTGAACC[G/T]GGGAGGCGAAGGTCG | 51070 |
rs568828368 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49567082 | CGGCCTCCCAAAGTG[C/G]TGGGATTATAGGCAT | 51070 |
rs568840203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PRRG2, NOSIP | GRCh38.p7 | 19:49582264 | AAAAAAAAAAAACTC[C/T]TGTGAAAAGTTTTGT | 51070 |
rs568930075 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSIP | GRCh38.p7 | 19:49560845 | GGGAGGGCATGTGGT[C/T]GCCAGGCCTCCTCCA | 51070 |
rs569356041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49573745 | ACATGTGAACACATT[C/T]GGTCCTCATGACAAC | 51070 |
rs569415542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49566213 | TTTTAGTGAAAACGG[A/G]GTTTCACCGTGTTAG | 51070 |
rs569438774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49565648 | CTGTAATCCCAGCTA[C/T]TCAGGAGGCTGAAGC | 51070 |
rs569524961 | in-del | -/T | | | downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555255 | GCGTTCTATTCAGGT[-/T]TTTTTTTTTTTTTTC | 51070 |
rs569684905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NOSIP, PRRG2 | GRCh38.p7 | 19:49579193 | CTTGACTCTGCACCA[C/T]GTAATGGATAGTAGT | 51070 |
rs569795325 | snp | C/T | | | upstream-variant-2KB, intron-variant | PRRG2, NOSIP | GRCh38.p7 | 19:49580882 | GATCGGGAAGCCCAC[C/T]TTCCCAAATATATCA | 51070 |
rs569864356 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSIP | GRCh38.p7 | 19:49556845 | CTGGCGCCCTGGCAC[C/T]GTGCGTGCCGGGGCG | 51070 |
rs569943136 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | NOSIP | GRCh38.p7 | 19:49570376 | GGAGCTCTCTCTCCC[A/C/T]CTACTGGCGTCTTCT | 51070 |
rs570021559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49578343 | TGGCCAGGCTGGTTT[C/T]GAACTCCTGACCTCA | 51070 |
rs570022188 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49564469 | AAAAAAAAAAAAAAA[A/T]AAAAAAACAAAATAA | 51070 |
rs570033984 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSIP | GRCh38.p7 | 19:49571127 | GATAACAGGCGCCCA[C/T]GCCCAGCTAATTTTT | 51070 |
rs570143135 | snp | A/T | | | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577727 | CCATGATCGAACCAC[A/T]GCACTCCAGCCTGGG | 51070 |
rs570150676 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | NOSIP | GRCh38.p7 | 19:49555643 | GTAGGAGCACTGTTT[C/G]CACGGCCCTGCATCC | 51070 |
rs570285071 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NOSIP | GRCh38.p7 | 19:49577640 | GCCGATGGCTCACAC[C/T]TGTAATCCCAGTACT | 51070 |
rs570377790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSIP | GRCh38.p7 | 19:49561831 | GGGGTTGCAGTGAGC[C/T]GACATCATGCCACTG | 51070 |