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 |