SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs149845444 | snp | G/T | 0.375 | 0.216506 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600833 | ATGCCTGGCAAATTT[G/T]TGTATTTTTAGTAGA | 6709 |
rs149862852 | snp | A/G | 3.29837e-05 | 0.00406088 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128583795 | TTCCATAGGAATAAA[A/G]CTTCGTGAAGCCAAC | 6709 |
rs149899658 | snp | A/G/T | 0.000132069 | 0.00812517 | missense | SPTAN1 | GRCh38.p7 | 9:128608925 | CAGCTCATCGCTGCC[A/G/T]GCCATTATGCCAAGG | 6709 |
rs150006796 | in-del | -/ATATA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570326 | TATATATATATATAT[-/ATATA]TTTTTTTTTTTTTTT | 6709 |
rs150008982 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630568 | ATGGAATCTCTCTCT[C/T]GCCCAGGCTGGAGTG | 6709 |
rs150023098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578693 | AGTTAGCTGGTCATG[A/G]TGGCACGCGCCTGTA | 6709 |
rs150074139 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599778 | TATTACCCCTTTGCA[A/G]ACAATCTTATGAGTA | 6709 |
rs150084377 | in-del | -/GGGG | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588963 | GCACAGAGAGTGGCT[-/GGGG]GTGTGTTTGTTCCAC | 6709 |
rs150097844 | snp | C/T | 0.000115343 | 0.0075933 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128607944 | CGGACACTATGCCAG[C/T]CCTGAGATCAAGCAG | 6709 |
rs150107885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572777 | ACACCATACCGGACA[A/G]CGTGGCGCCCCATAG | 6709 |
rs150119450 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628751 | GAAATAGACCCATCC[A/G]GCCGGGCCACACATT | 6709 |
rs150149688 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613802 | TGAGGTCAGGAGTTC[A/G]AGACCACTCCGGCCA | 6709 |
rs150275002 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564159 | TGCGTGGTGGCTCAC[A/G]CCTGTAATCTTAGCA | 6709 |
rs150276985 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590182 | TTTATCCTTGTCATG[A/G]TAATTTGAGGAAACC | 6709 |
rs150287999 | snp | C/T | 3.29679e-05 | 0.00405991 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128578218 | GGCTGGGGCTGAAGC[C/T]CTGCTAGATAGACAC | 6709 |
rs150323605 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595929 | GCTTACTGCAGCCTC[C/T]GCTTCCTGGGCTCAA | 6709 |
rs150338566 | snp | G/T | 1.64732e-05 | 0.0028699 | missense | SPTAN1 | GRCh38.p7 | 9:128584783 | TTACAAGCAGAAATT[G/T]CTGGACATGAACCAC | 6709 |
rs150339907 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582424 | TACTTTTCTCCAGAG[C/G]CCAAGCTTGGGACTA | 6709 |
rs150387180 | in-del | -/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626818 | TTTCATCAGAAGTTT[-/C]CATTTCTTTTTGTGT | 6709 |
rs150413188 | snp | A/G/T | 0.00358779 | 0.0422022 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587111 | CAGGCGTGAGGCACC[A/G/T]CGCTCGTTCTGTCGC | 6709 |
rs150427953 | snp | A/G | 1.6476e-05 | 0.00287014 | missense | SPTAN1 | GRCh38.p7 | 9:128615768 | TGGCGGCCTCCCGGC[A/G]AGCCAAGCTGAATGA | 6709 |
rs150489136 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623754 | GCTAGGATTACAGGC[A/G]TTAGCCACTGCGCCT | 6709 |
rs150522117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621697 | CTAGATCAAACAGCC[A/G]CAGACTCCCGTTTAA | 6709 |
rs150585404 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602697 | CTGGAGTGCAGTGGC[A/G]CAATCTCAGCTCACT | 6709 |
rs150595456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565346 | TTGGGAGTGGCATGG[C/T]GAAGAATGTTTCCTT | 6709 |
rs150632298 | in-del | -/AGG | 0.0368353 | 0.130617 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586034 | ACTGAGAAGGAAGTT[-/AGG]AGAAGTAGTGATGCG | 6709 |
rs150679083 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585492 | ACTAGTCTTTATGAT[A/G]CTATCACTAATGCCA | 6709 |
rs150731568 | snp | A/G | 0.00079272 | 0.019893 | SPTAN1 | 9 | allele_origin=G(germline)/A(germline) | 9:128588817 | TTTTTAGCAACAAGT[A/G]GCCCCCACGGATGAT | 6709 |
rs150793549 | snp | G/T | 0.000399281 | 0.0141238 | missense | SPTAN1 | GRCh38.p7 | 9:128568839 | GAGCCATTGTTAAGC[G/T]GGATGAAACTGGAAA | 6709 |
rs150801649 | snp | C/T | 0.000627622 | 0.0177036 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128625780 | TCAGGAAACTTTTGA[C/T]GCTGGGCTGCAGGCC | 6709 |
rs150870424 | snp | G/T | 0.000148245 | 0.00860815 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128591512 | GAACGATCGTCAGGG[G/T]TTTGTGCCGGCTGCG | 6709 |
rs150891208 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616681 | CTGAGGCAGGATAAT[C/T]GCTTGAACCAGGGAG | 6709 |
rs150902677 | snp | C/T | 0.00100464 | 0.0223899 | SPTAN1 | 9 | allele_origin=T(germline)/C(germline) | 9:128625858 | TCTCGCCGCCAAACA[C/T]GTTCAGTCCAAGGCC | 6709 |
rs150944593 | snp | C/T | 6.58892e-05 | 0.00573936 | missense | SPTAN1 | GRCh38.p7 | 9:128607632 | TGGATCAATGGAATA[C/T]GGGGGTTGGTGTCCT | 6709 |
rs150960451 | snp | C/T | 1.648e-05 | 0.0028705 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128618982 | CAGCGAAGATTATGG[C/T]GACACTCTTGCCGCC | 6709 |
rs150991904 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586643 | TGTACATACCAGTGC[A/G]CACATATACCCACAT | 6709 |
rs151012062 | snp | C/G | 3.29473e-05 | 0.00405864 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128630324 | TTCCACGTTTAGGTC[C/G]TGTATGGTGGAAGAG | 6709 |
rs151065983 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596946 | AGGCAGATCACCTAA[G/T]GTCAGGAGTTCGAGA | 6709 |
rs151150353 | snp | C/T | 4.94629e-05 | 0.00497283 | missense | SPTAN1 | GRCh38.p7 | 9:128576946 | GCAGCAGAAGTTCAG[C/T]GCTTTAACAGGTGTC | 6709 |
rs151161562 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575033 | AATGCCGTGAACTCA[A/G]CCTCTTAACTTTCTG | 6709 |
rs151191878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630491 | TATTATTGTACCCTT[C/T]TCCCTTGGCCTAAAG | 6709 |
rs151206158 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618307 | TTCATCTGGACCCAC[A/T]GTATGAGTCCAGAAT | 6709 |
rs151215019 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582098 | CTTAATGGAAACCTC[C/G]AAACTTCTTTAAGTT | 6709 |
rs151318628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603697 | CGGGTGACCTGTGAC[A/G]TATCTCACTCTATTG | 6709 |
rs180835590 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573308 | CTGGGAAGTGAATAC[A/G]TTTGACCCTGTGGCT | 6709 |
rs180843381 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563627 | GATTCGTTATGGAGC[C/T]CTCTCCCTACCCCTT | 6709 |
rs180864378 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587884 | AGAGTCTCACTCCGT[C/T]GCCTAGGCTGGAGTG | 6709 |
rs180940724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629482 | TAACCCTGGCTCGCC[A/G]GGTTTTAAAAGGGTA | 6709 |
rs181077220 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561098 | ATGTCGGCCAGGCAC[A/G]GTGGTTCACGCCTGT | 6709 |
rs181093445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612957 | TTTTTTAATAATTGC[A/G]TAAGTTTATCATAGA | 6709 |
rs181105962 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567839 | AATCTCAGCTCACTG[C/G]AACCTCTGCCTCCCA | 6709 |
rs181117376 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591362 | TGAGCCACTGTGGCC[A/G]GCCGTTTTGGACCTC | 6709 |
rs181157159 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624653 | AGGAGGAGACAGTGT[A/C]CTGAGGCCAGAACTG | 6709 |
rs181165486 | snp | A/G | 0.000149881 | 0.00865553 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581936 | AATGACCCTTATAGT[A/G]AGCCAGAGTCTTTTT | 6709 |
rs181169105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604489 | ACAGCCCCCAAGCTT[A/G]CTGACTGAGATCCTA | 6709 |
rs181176570 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633632 | AATCTGTTTTCATGT[A/G]AAAGACAAATAAATG | 6709 |
rs181327424 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562882 | AGGCAGGAGAATGGC[A/G]TGAACCCAGGAGGTG | 6709 |
rs181382502 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628901 | CTCCGTGAGGTGCCA[C/T]GCTCCCCTCACCTTA | 6709 |
rs181384727 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586772 | ATAGTTCCTGTACCT[A/G]GCTCTTACCACTCTT | 6709 |
rs181391744 | snp | A/C/T | 3.29538e-05 | 0.00405904 | missense | SPTAN1 | GRCh38.p7 | 9:128607927 | CAGCAGCTGTTGGCT[A/C/T]ACGGACACTATGCCA | 6709 |
rs181397898 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621312 | GACACCCACGTGTTG[G/T]TACCACAGAGGTCCC | 6709 |
rs181402160 | snp | C/G | 4.94491e-05 | 0.00497213 | missense | SPTAN1 | GRCh38.p7 | 9:128574690 | ACCCGTTTGATGGAG[C/G]TGCACCGCCAGTGGG | 6709 |
rs181507041 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592469 | TAGTAGAGATGGGGT[A/T]TCACTGTGTTGGCCA | 6709 |
rs181510468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597738 | ACTGTAACCTCTGCC[A/G]CACCCCGGTTCAAGC | 6709 |
rs181554749 | snp | A/C | 0.00159617 | 0.0282053 | utr-variant-5-prime | SPTAN1 | GRCh38.p7 | 9:128552594 | GCGTCGCCGCCACTA[A/C]CCGCTGCGGAGTGAA | 6709 |
rs181578150 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616403 | GTGCTGTGATCACAG[G/T]CATGAGCCACTGCGC | 6709 |
rs181597099 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560107 | TTTTTTTTAAGAGAC[A/T]GAGTCTCGCTCTGTC | 6709 |
rs181699065 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603325 | ACTCTTCATCAGATA[A/C]AATTAATTACTCAGT | 6709 |
rs181700435 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569087 | ATGCAAGCGTTTGTA[C/T]ACTCAGTGAGGAAAT | 6709 |
rs181729340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596345 | GCAGTGGCGCAATCT[C/T]GGCTCACTGCAACCT | 6709 |
rs181782458 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624137 | AAAGTAGAATTGTCA[A/G]TACGTGTATTTGTGT | 6709 |
rs181793891 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564627 | AAATATTAGGTTGCT[C/T]GGTGTAATCATACCT | 6709 |
rs181796543 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620893 | GATGACAAAGGGTTT[G/T]ACCCTTCCCAAAGGT | 6709 |
rs181799534 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588625 | CAAAATGAGATTTTT[A/T]TTTTAAAGATACCAA | 6709 |
rs181863978 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581215 | TTCTCTCAGCTCTGC[C/T]AGCATCTCTCCCTGC | 6709 |
rs181963662 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630463 | CTGGCTTAAAGTCAG[A/G]AACCAGATGTGCTAT | 6709 |
rs181982235 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592182 | GAATAGTGAAATTTT[G/T]GGGCTCCAGTGATCC | 6709 |
rs181989946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615518 | AGAGGTCCACATAAC[A/G]GACTTTGAGAATATC | 6709 |
rs181992677 | snp | C/T | 0.000793926 | 0.0199081 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568740 | GATGCTGTGTGGTTG[C/T]GTCTGAGGCTCACTT | 6709 |
rs182199405 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573676 | GGCCAGGCTGGTCTC[A/G]AACTCCCGACCTCCT | 6709 |
rs182226889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624825 | CCACCCAGCTCCTGG[A/G]TGAGGGAAAACTGGG | 6709 |
rs182254267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128555018 | TCCTGGGATCCTCAG[A/G]AGGAAGGCATGTTTA | 6709 |
rs182256701 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575557 | TTGGGCAGGAAGGGC[A/C]GAGTTCATTTGATCT | 6709 |
rs182272113 | snp | A/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128608959 | ACATTTCTAGCCGGC[A/G]CAATGAGGTCTTGGA | 6709 |
rs182324989 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621818 | GAGAAAAAATAAAGG[C/G]GCTTGGTGCTTTCTC | 6709 |
rs182403113 | snp | A/G | 0.00024707 | 0.0111119 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584688 | ACTTTTCTCTTCATG[A/G]TTGGATAACTGGGGA | 6709 |
rs182410884 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606114 | CGGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 6709 |
rs182414615 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561759 | CATATTCTGGGAACC[A/G]GAGGATCCCAGGTCA | 6709 |
rs182480392 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626817 | GTTTCATCAGAAGTT[C/T]CATTTCTTTTTGTGT | 6709 |
rs182490893 | snp | A/G | 0.00178214 | 0.0297976 | downstream-variant-500B, utr-variant-3-prime | SPTAN1, WDR34 | GRCh38.p7 | 9:128633729 | CGAAGGCTTGCACCC[A/G]CCTCCCGGGACCCCT | 6709 |
rs182591461 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610784 | CAGTAAAATAAATTC[A/C]TTCCTGCAGTCAAGC | 6709 |
rs182623553 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589690 | ACGCCATTCTCCTGC[C/T]TCAGCCTCCCGAGCA | 6709 |
rs182626203 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558038 | TCAATCTCCTGACCT[C/T]GTGATCCATCTGCCT | 6709 |
rs182641854 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565322 | AAACAAAAAAAAGCC[A/G]TAAAAGATTTGGGAG | 6709 |
rs182692245 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630980 | TCCCAAAGTGCTGGG[A/G]TTACAAGCGTGAGCC | 6709 |
rs182701478 | snp | C/T | 0.00117353 | 0.0241948 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609326 | CTTGATGTAGCCTTA[C/T]GTTATTGAGTAGATT | 6709 |
rs182851964 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593289 | TGGTGTTGGTTCTCC[C/T]TCCTGTTGGTTTTTG | 6709 |
rs182875801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631360 | GCTACTCAGGAGGCT[A/G]AGGCAGGAGAATCAC | 6709 |
rs182887964 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590679 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAATAC | 6709 |
rs182918077 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561482 | TCCTGGCTAATATGG[G/T]GAAACCCCATCTCTG | 6709 |
rs182926833 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583593 | TTATATCTCAAGGGG[A/G]TTAGAATGCTTCCAG | 6709 |
rs183044273 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618765 | TGGGATTGCAGGCAT[G/T]AGCCACCATGCCCAG | 6709 |
rs183144590 | snp | G/T | 0.000329679 | 0.0128348 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617948 | ACAGAAGCACCAGAA[G/T]AGCTACCTGCTGTTA | 6709 |
rs183149137 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569466 | ATTTTAGTGCGAGTT[C/T]ATTGGAGCTGAGGTA | 6709 |
rs183177675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623160 | TCCCGGGTTTCAGCA[A/G]TTCTCCCACCTGAGC | 6709 |
rs183262348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622541 | TGACCTCAGGTGATC[C/T]GCCCTCCTCGGCCTC | 6709 |
rs183443928 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601461 | GCTAGGTGTTGTGGC[C/T]CACACCTGTAATCCC | 6709 |
rs183467947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605533 | CTTCTTTGTAGGGGT[C/T]ATTTTTATTGTGAAA | 6709 |
rs183488000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620290 | CACCTTCCTCACCAT[A/G]GGAAGCATCCTCCCG | 6709 |
rs183502405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570275 | ACTTTATTCATGTCT[A/G]TTAGTACCCTCTGCC | 6709 |
rs183550589 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618357 | GTCCAGAATCACACA[C/T]GAATCACACATGAAT | 6709 |
rs183566381 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593906 | TGTGGTTGTGTTGTT[A/C]TAAGTGCAGAATCGG | 6709 |
rs183627578 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602638 | GTTTTTATTTGTATT[G/T]TATTTATTTATTTTC | 6709 |
rs183633533 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558703 | TCTCTGTGAAGTCGG[C/T]CTTATCAGTCTGCTG | 6709 |
rs183637774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579322 | TCTATAAAATCATAG[C/T]AAACAAGTCCATTTG | 6709 |
rs183695592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626100 | AGTGCAGAGCTTTCA[A/G]ACATGGGTGTGGCTG | 6709 |
rs183699823 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594608 | GCTAATTTTTGTATT[C/T]TTTGGTAGAGACAGG | 6709 |
rs183701883 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623321 | CTCAAGTGATTCTCT[C/T]GCCTTGTGCTGAAAT | 6709 |
rs183713949 | snp | C/T | 3.29511e-05 | 0.00405887 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600136 | AACTCCTTTGCAAAT[C/T]ATTGTTTTCAAGAGT | 6709 |
rs183734316 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557133 | TATGAATTTTTCCAT[A/T]ACCAAATGACCAAAC | 6709 |
rs183925733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577690 | TCATGTGTAGTATAC[A/G]TATGGTATTTACAAC | 6709 |
rs184011016 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582240 | GCCAGGAGATCGTGC[C/G]ACAACTAATGTCTCC | 6709 |
rs184068161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608500 | GGGATGGAAAACAAA[C/T]GTGTGGGTAGGTAAG | 6709 |
rs184078955 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628946 | CCCTGCCCATCTTGC[C/G]CATTCCTAGTGTGAG | 6709 |
rs184085066 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587315 | GTCTTGAACTCCTGG[A/G]CTCAAGCTGTCTGCC | 6709 |
rs184156355 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604855 | AGAATCACTTGAACC[C/T]GGTGGGGGCGGAGGT | 6709 |
rs184184506 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561313 | GGAGGCGGAGGTTGC[A/G]GTGAGTCAAGATCGC | 6709 |
rs184307340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612429 | GGGAGTGAATGTTAA[A/G]AGAGCTGACTTGTAG | 6709 |
rs184324003 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591278 | TCACTGTGTTGGCCA[G/T]GATGGTCTCCATCTC | 6709 |
rs184431265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614539 | AGGTTGCAGTGAGCC[A/G]AGATTGTGTAACTGT | 6709 |
rs184440576 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567855 | AACCTCTGCCTCCCA[C/G]ATTCAAGTGATTCTC | 6709 |
rs184532140 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633633 | ATCTGTTTTCATGTA[A/G]AAGACAAATAAATGA | 6709 |
rs184535963 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562788 | GCTAGCACGGTGAAA[A/C]GCCATCTCTACTAAA | 6709 |
rs184544691 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586642 | ATGTACATACCAGTG[C/G/T]GCACATATACCCACA | 6709 |
rs184577750 | snp | A/G | 4.95618e-05 | 0.00497779 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591637 | ATCAGTAAGGATGAC[A/G]CTGGGGGCCGCAAGG | 6709 |
rs184626371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607202 | AGAGACAGGGTTGCA[C/T]CACATTGCCCAAACT | 6709 |
rs184675224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595293 | TTTTGTATTTTTAGT[A/G]CAACCGGGATTTTGC | 6709 |
rs184764990 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566417 | ACAGTTGCTGTTTCC[A/T]CTGAATCCTTGAAGC | 6709 |
rs184821048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619446 | ATGTTCTGCAAACCT[A/G]TAGGGGAGGATCTTT | 6709 |
rs184824782 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572140 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCACCC | 6709 |
rs184842514 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596272 | TGTTTTGTTCGTTTT[G/T]TTTGTTTGTTTGTTT | 6709 |
rs184850735 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573486 | CCCGAGATGGATTCT[C/T]GTTCTGTTGCCCAAA | 6709 |
rs184854265 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591123 | CTGGAGTGCAGTGGC[A/G]CAATCTCAGCTCACT | 6709 |
rs184863049 | snp | A/C | 0.000399281 | 0.0141238 | missense | SPTAN1 | GRCh38.p7 | 9:128611716 | TTGGTATTTTTAGAG[A/C]AAGCACCAGAAGCAC | 6709 |
rs185066020 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567503 | TGCCATGTTGGCCAG[G/T]CTGGTCTTGAACTGA | 6709 |
rs185118570 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622085 | CAACAATGTAGCTAA[A/C]ATCCACTTCACTGGA | 6709 |
rs185133273 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599599 | TTATAGCCTACTGCA[G/T]CCTCGAACTCTTGGC | 6709 |
rs185139756 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128556057 | AAACCCCATCTCTAC[C/T]AAAAATACAAAAAAT | 6709 |
rs185148066 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575875 | AGCTGCTTCCACTAC[A/G]AGTCCAAAGGGTTCC | 6709 |
rs185186184 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570931 | CTCCCAAAGTGCTGC[A/G]ATTACAGGCATGAGC | 6709 |
rs185363868 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628556 | GAGCAGGGCTGGGCT[A/G]TCCCGCCCAGTCCCG | 6709 |
rs185369614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624750 | ATGGCATAATGTGAC[A/G]TCATGGCATGAACAA | 6709 |
rs185379907 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582229 | GTTTGACCCCTGCCA[A/G]GAGATCGTGCCACAA | 6709 |
rs185387751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604524 | AACTGCTGGCTCTTA[C/T]TGATGTTTATTTGTG | 6709 |
rs185389294 | snp | C/T | 0.029116 | 0.117091 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561144 | GGAGGCCGAGGCGGG[C/T]GGACCACAAGGTCGA | 6709 |
rs185471840 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603033 | TGAAAGCTAATTCAC[A/T]GCTTTATTTTTTCCC | 6709 |
rs185501795 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631920 | CCAGCTGCTTTGGAA[A/C]CCTCACATTGAAAGT | 6709 |
rs185504943 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559363 | CAGATGGAACCTTTG[C/T]GATATTATGATGGAG | 6709 |
rs185610118 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623737 | CCTCAGCCTCCCAGA[A/G]TGCTAGGATTACAGG | 6709 |
rs185614333 | snp | C/T | 8.24695e-05 | 0.0064209 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128580936 | GCTGACCGTCCTTTC[C/T]GAGGAGAGAGCGGCG | 6709 |
rs185616033 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574953 | GTGGGGTTGCTGTCT[C/G]TCCAGCTGCTCTCTA | 6709 |
rs185624147 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554107 | AAAAAAAAGTGCTGC[A/G]GTAAAGGCCTCTGTG | 6709 |
rs185688203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616631 | AATTAGCCAGGTGTG[A/G]TAGCAGGCGCCTGTG | 6709 |
rs185728615 | snp | A/G | 0.00174047 | 0.0294484 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628053 | CTTCCTGCCCAGGGC[A/G]GGCTGCACTTCCCCT | 6709 |
rs185736929 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585173 | GGACACACCACCATA[C/G]CCAGCTAATTTTTGT | 6709 |
rs185769071 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629572 | ACCGTGTGATTCGTC[C/G]CTGCACGTAACCCTA | 6709 |
rs185797321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587960 | AAGCGATTTTCCTGA[C/T]TCAGCCTCCTGAGTA | 6709 |
rs185852502 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581734 | TCACAGTCTTAGAAG[A/T]TCAAAGGAATAGGAC | 6709 |
rs185854695 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606593 | GGTTCAAGCGATTCT[C/T]CTGCCTCAGCCTCCC | 6709 |
rs185883819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562109 | TTGGACTCAGAGATC[C/T]GTATGATTTGTTTTT | 6709 |
rs185915717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608819 | TCAAGACTGGCAGTC[C/T]AGGCAGGGCCCAGCC | 6709 |
rs185917355 | snp | C/T | 0.000704183 | 0.0187509 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588978 | TGTGTGTTTGTTCCA[C/T]GCTGGCACCTCCACG | 6709 |
rs185925523 | snp | G/T | 0.000461566 | 0.0151845 | SPTAN1 | 9 | allele_origin=G(germline)/T(germline) | 9:128608981 | GGTCTTGGACAGGTG[G/T]GTGTCCTGTGGCACT | 6709 |
rs185926700 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564158 | GTGCGTGGTGGCTCA[C/T]GCCTGTAATCTTAGC | 6709 |
rs185995000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630744 | GTTTCACTCTTGTTG[C/T]CCAGGCTGGAGTGCA | 6709 |
rs186100440 | snp | C/T | 3.29717e-05 | 0.00406015 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617979 | ACCTCCTCGTCCTTG[C/T]CTGTCAGGGTGTCCT | 6709 |
rs186163057 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592253 | TTACTATAGAGATAA[A/G]AATGGGAGGTTTTGG | 6709 |
rs186180680 | snp | A/C | 1.64803e-05 | 0.00287052 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568907 | ATACGGGTGAGTATG[A/C]GTAGCTCGTGGAGTG | 6709 |
rs186245014 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615970 | CTTGGGCACACAGTC[A/G]TGGGATGCCTCAGTG | 6709 |
rs186293166 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562943 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC | 6709 |
rs186340527 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597929 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCACCC | 6709 |
rs186552628 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621404 | CCATTCCTGTGTTTC[A/G]TGACAAGTTGGATAT | 6709 |
rs186562810 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624580 | TGCAGAGAAGAAACT[A/G]ATCAATTGTGGGCAT | 6709 |
rs186574182 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592516 | CTGACCTCGTGATCC[A/G]CCCGCCTTGGCCTCC | 6709 |
rs186753752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606141 | CTTTGGGAAGTCAAA[A/G]CAGGTGGATCACGAG | 6709 |
rs186760576 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627240 | ACCAAGTGCTCTGAG[C/G]CGGCCTCATGTCTCC | 6709 |
rs186769459 | snp | A/G | 0.00228925 | 0.0337548 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584879 | ACATGGCTTGGTGCT[A/G]CTCCTCGTGTCTCCC | 6709 |
rs186795271 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569271 | GACACTATAAAGAAG[G/T]TTATCTGTGGGAAAG | 6709 |
rs186805427 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128556198 | TGCACTCCAGCCCAG[A/G]TGACAGTGCGAGACT | 6709 |
rs186836922 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620930 | ACTGTCCCTGCTGAA[G/T]CCTGTCCCACCACTG | 6709 |
rs186963184 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631042 | TAGAGACAGTGTTTT[A/G]CCTTGTTGGCCAGGC | 6709 |
rs186965508 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602008 | TTACCCCCTCAACAG[A/T]ATGTTTCTGATAACA | 6709 |
rs186974727 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609408 | GTGAGAAATATTTCA[A/G]TAAGCCCAGCCAGTG | 6709 |
rs186978001 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558276 | GCATTACTTGCTGAA[C/T]GATGCAGCTAACGTT | 6709 |
rs186987404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578955 | ATTTTTAAAAATACT[A/G]CTTATTAGAGCAGAA | 6709 |
rs187051071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596364 | TCACTGCAACCTCCA[C/T]CTCCCAGGTTCACGC | 6709 |
rs187054577 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128550609 | AGCAGCAGAACCCCC[A/G]GTTCACTATGGGGCC | 6709 |
rs187102260 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561338 | GATCGCACCACTGCA[A/G]TCCAGCCTGGCGACA | 6709 |
rs187163498 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604907 | ATTGTGCTCCAGCCT[A/G]GGTGACAAGAATGAA | 6709 |
rs187206562 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605821 | ACATGGCGAAATGCC[C/G]TCTCTACCAAAAGTA | 6709 |
rs187218555 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561612 | AGCTTGCAGTGAGCC[A/G]AAATTGCACCACTGC | 6709 |
rs187221412 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583720 | CACTAAGATACTACT[A/G]TTCATGGGCAGTGTT | 6709 |
rs187278754 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626215 | AGGGTAGGAAGGGGA[A/G]AAAAGGCTGGTGAAG | 6709 |
rs187375163 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624954 | CCTGGGTGCAGGGAG[G/T]GGCCTGCTAATGTGG | 6709 |
rs187383340 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582640 | AAGTCTCTTCAACTG[G/T]ATATCCCTTTGGGAG | 6709 |
rs187440376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591000 | GTGACCCTCTGCAGG[C/T]ATGGCAGGTGAGGAA | 6709 |
rs187515853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631490 | GCATGGTGGCCTACA[C/T]CTGCTCAAAGTCCAG | 6709 |
rs187613754 | snp | C/G/T | 0.000743712 | 0.0192703 | SPTAN1 | 9 | allele_origin=T(germline)/C(germline) | 9:128632799 | GGCTCTTGCTTCCCC[C/G/T]GCTCCTAGAGATGGC | 6709 |
rs187615303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591242 | AATTTTTTTTGTATC[C/T]TTTTTAGTAGAGACG | 6709 |
rs187618515 | snp | C/T | 0.000494805 | 0.0157212 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611890 | GAGGAAGATGACCAC[C/T]GTCACTGTCAACCTG | 6709 |
rs187627393 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566422 | TGCTGTTTCCTCTGA[A/T]TCCTTGAAGCCTTTG | 6709 |
rs187639125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569567 | CAGTGAGGTGTGCAC[A/G]TTGAGTTTCTTATAA | 6709 |
rs187686066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565839 | TGTTCTGCTTCCTTA[A/G]TGAACTCAAAAACCT | 6709 |
rs187763623 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611260 | CGATTGCTTGAGCTC[A/G]GGAGTTCAAGACCAG | 6709 |
rs187848379 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618705 | AGCCAGGATGGTCTC[A/G]ATCTCCTGATCTCGT | 6709 |
rs187860797 | snp | C/G | 0.000380842 | 0.0137941 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594127 | ATGTTAGCATCTACA[C/G]CTAACTGCCTTCCTT | 6709 |
rs187876904 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570432 | AACCTCCACCTCCTG[A/G]GTTCAAGCAATTCTC | 6709 |
rs187974678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565741 | TAAAGGAAAGAACTC[C/T]CAGATGTTTCCAGGG | 6709 |
rs188005683 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593515 | TTCGTGTTCAAAGAT[A/T]ATATTTCAGCCTTTT | 6709 |
rs188013732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561835 | ACTTAATTATAAAAC[A/G]ATGGCAGTTTCTTTA | 6709 |
rs188015502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568560 | GTGAGGACCATTGAT[A/G]GCCCTCGCTGGCCAG | 6709 |
rs188021276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623427 | AAATAATACTAATGA[A/G]TATATCATCTTAACT | 6709 |
rs188033225 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579429 | GTGACCTGAAAAGCC[A/G]TTTGGAAAGGATTTC | 6709 |
rs188040592 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602650 | ATTTTATTTATTTAT[A/T]TTCGAGTCGGAGTCT | 6709 |
rs188247443 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589732 | AGGTGCCTGCCACCA[C/T]GCCCGGCTAATTTTT | 6709 |
rs188273512 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573194 | CATTGAGGTTGGATT[A/G]GAATACCAGAATGCA | 6709 |
rs188277043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594649 | GTTGGCCAGACTGGT[C/T]TCAAACTCCTGACCT | 6709 |
rs188302998 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623227 | ACACCTGGCTAATTT[C/T]TTTCTTTTTTTCTTT | 6709 |
rs188465709 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, missense | SPTAN1 | GRCh38.p7 | 9:128629139 | GCATAGCATATCGTC[A/G]GGTCATTCGTGTCTA | 6709 |
rs188511918 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622607 | CCCGGCCAGCGAGCC[A/G]GCTGCTTTGTCCTCA | 6709 |
rs188514436 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578332 | TGAGGCCTATAGTCG[C/G]CGTTGGTACCATGTT | 6709 |
rs188544996 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619258 | GGCAGCGCTGTGGGC[C/T]TGAGTCTTCATATCA | 6709 |
rs188555057 | snp | A/G/T | 0.00318978 | 0.0398085 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571156 | TTAGTGGGGCGTGGT[A/G/T]GTGCACACCTGTAGC | 6709 |
rs188680809 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624611 | GGCAGAGAACCTACT[A/C]CCAGGGCAGACCACT | 6709 |
rs188688870 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633483 | GTGCTTCACTAACCC[A/G]CTTCCGGTCCAGTCA | 6709 |
rs188698554 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603938 | CTCTTCCCAGGCCTG[C/G]TCTGGCCTGAGAGTC | 6709 |
rs188709020 | snp | G/T | 4.94173e-05 | 0.00497053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581769 | TTCTGAACACTTTGT[G/T]TCCTTTGGCAAGGCG | 6709 |
rs188719496 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557196 | CTTTCTTGCAAAACT[C/G/T]TATGTCTAGTGGTGT | 6709 |
rs188785098 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600293 | TGCTTAATATACAAA[A/T]GCAGAGTGTCTGTCA | 6709 |
rs188816972 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606737 | GTGATCCACCCACCT[C/T]GGCCTCCCAAAGTGC | 6709 |
rs188930473 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628808 | GGGATCGCAGTTTCC[A/G]GCCTGTGCCCGTAGG | 6709 |
rs188938153 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586716 | ACTGGTTATCTGTTT[C/T]TTGACTAAAATTCTC | 6709 |
rs188946441 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607788 | CCCTTTGTGGTGAGT[C/T]GGTGGTTGACGTCAG | 6709 |
rs189011481 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585320 | AGCCATGAGCCACCG[C/T]GCCTGGCTCCGAGCC | 6709 |
rs189027301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591773 | TTGAGCCCACAGACC[C/T]CCCTGTGTGGGTCTC | 6709 |
rs189060902 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558875 | AATTCTTAATGATAT[C/T]TATGAGAATTTTCCT | 6709 |
rs189082273 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628362 | GGCAGTGCTGGGGGC[C/T]CAGGCAGGGTACAGT | 6709 |
rs189104921 | snp | C/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633658 | AAATGATGACTTCCC[C/G]CAAAGCTTTGCTTTT | 6709 |
rs189284010 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619783 | ATACTCCCTAAATTG[A/G]TTAACTGTTGCTACA | 6709 |
rs189317937 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615282 | AACTTTCACTGCCTT[C/T]TTAAGGACATTTTTA | 6709 |
rs189339906 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620365 | CCATCCTCTGCATAG[G/T]TGAGTTCCCTGGAAG | 6709 |
rs189355116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596338 | CTGGAGTGCAGTGGC[A/G]CAATCTCGGCTCACT | 6709 |
rs189363458 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587882 | ACAGAGTCTCACTCC[A/G]TCGCCTAGGCTGGAG | 6709 |
rs189368182 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573556 | CCACCTCCCAGGTTC[A/G]AGCAATTCTCCTGCC | 6709 |
rs189529449 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567765 | ATTATATATTTAAAA[C/G]TTTTTTTTTTTTGAG | 6709 |
rs189557556 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595491 | ATGCTATGTTCTCTA[C/T]ATGTTGTTATAAGAA | 6709 |
rs189564884 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563406 | GGCAACAGAGTGAGA[A/C]CCTGCCAAAAAACAA | 6709 |
rs189600485 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612857 | TTGAACCTGGGAGGT[A/G]GAGGTTGCAGTGAGC | 6709 |
rs189634683 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608709 | AATGAAATCAAGCTT[G/T]CTTTTGGCATTTTAC | 6709 |
rs189759548 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593708 | AGATAAAACATCCTA[C/T]ATGAGGATATTTTAA | 6709 |
rs189780459 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624808 | TGCCCTGGTCAGGGG[C/T]GCCACCCAGCTCCTG | 6709 |
rs189782393 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569580 | ACGTTGAGTTTCTTA[A/T]AACTGGATGTACTTA | 6709 |
rs189795391 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604620 | TAGCCACAGACAAAT[A/G]TACAAATGTCAGCTA | 6709 |
rs189888960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591323 | CACCCGCCTCGGTCT[C/T]CCAAAGTGCTGGGAT | 6709 |
rs189996830 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621532 | TATTTCTCAAGCAAT[A/G]CAGTCTCTTTATAGG | 6709 |
rs190012740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597968 | TTGTTTTGTTTTTGA[A/G]ATGGAGTTTCGCTCT | 6709 |
rs190026506 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554513 | AAGTTGGGGGTCAAC[C/T]GCAGATCCTGAAAAG | 6709 |
rs190033447 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575411 | TTAGTATATTCAGGA[A/T]AAAATTTTGATGATT | 6709 |
rs190095230 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574588 | TCAGCGCTCCATAAG[G/T]TCTCTAACTTGTCTA | 6709 |
rs190096460 | snp | A/G/T | 0.000941456 | 0.0216763 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581101 | TGGTGGGAGAAGAAG[A/G/T]GCCTGTGTTTTGCCT | 6709 |
rs190171359 | snp | A/G | 1.65913e-05 | 0.00288017 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626341 | CTCCTGCACTGCGTC[A/G]GCACGTCCAGCCCTG | 6709 |
rs190185343 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623903 | CCAGCCTGACCAACA[C/T]GGTGAAACCCCCATC | 6709 |
rs190190098 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606099 | CTCTGCAGCCGGGCA[C/T]GGTGGCTCACGCCTG | 6709 |
rs190341376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562227 | TCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGGCTA | 6709 |
rs190358523 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560029 | TGTGAGCCACCCTGC[C/G]TGGCCGATAATTTTG | 6709 |
rs190403400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630835 | TCAACCTCCCAAGTA[A/G]CTGGGATTACAGGCG | 6709 |
rs190423154 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603134 | GATGAAAGTGATTAT[C/T]AGAGCTCCTGGCTGT | 6709 |
rs190430347 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589549 | CCAAAGTGCTGGGAT[C/T]ACAGGCATGAGCCGC | 6709 |
rs190436926 | snp | A/G | 1.70942e-05 | 0.00292349 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609320 | GTTGGTCTTGATGTA[A/G]CCTTATGTTATTGAG | 6709 |
rs190447429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565208 | CTCGGGAGGCTGAGG[C/T]AGGAGAATCACTTGA | 6709 |
rs190643546 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561278 | CTCGGGAGGCTGAGG[C/G]AGGAGAATTGCTTGA | 6709 |
rs190661516 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615998 | GTGTCTTCTGCTTTC[C/T]GGGTTTACAGTGATG | 6709 |
rs190676025 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592350 | TGTGATCTTGGCTTA[C/G]TGCAACCTCTGCCTC | 6709 |
rs190696993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569079 | CAGCATGAATGCAAG[C/T]GTTTGTATACTCAGT | 6709 |
rs190939297 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590222 | TATCTTTCTATTGAG[A/T]CTAATTTAAACCTAA | 6709 |
rs190959808 | snp | C/G | 0.000636641 | 0.0178302 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618157 | AGTGGAAGGCCAGCA[C/G]CCAAGGGCAGACTCT | 6709 |
rs190969635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582236 | CCCTGCCAGGAGATC[A/G]TGCCACAACTAATGT | 6709 |
rs191029857 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631140 | ATGAGCCACCACTCC[C/T]GGCCGAGGGCTCTTC | 6709 |
rs191112872 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622330 | TTGCGACGGAGTTTC[A/G]CTCTTGTTGCCCAGG | 6709 |
rs191186256 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569316 | TCTTGGCTTGCCCTG[A/G]GAGGGGTTTACGTCT | 6709 |
rs191196129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565762 | GTTTCCAGGGTAACA[C/T]AATTTTATACCTTTT | 6709 |
rs191245287 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619797 | GGTTAACTGTTGCTA[C/T]ATAACAACCCGCCTA | 6709 |
rs191259998 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596133 | ACAGGTGTGAGCCAC[C/T]GCACCCGGCCCATAA | 6709 |
rs191265660 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609499 | AAAACTATTTCTGCT[A/G]TAATAAAAGTCTATA | 6709 |
rs191278313 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616682 | TGAGGCAGGATAATC[A/G]CTTGAACCAGGGAGG | 6709 |
rs191281147 | snp | A/C/G | 0.000230621 | 0.0107359 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628005 | GTGCGCTTGCCCCTC[A/C/G]TGGCCTGGCTTGTGG | 6709 |
rs191432357 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592603 | ACCAGTAGTCTGGGT[C/T]ATAAATATAAGAGGA | 6709 |
rs191456019 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128551613 | ATCTCATAAAATTAT[G/T]GCAAAGATTAAGAAA | 6709 |
rs191494910 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623294 | TGCCCAGGCTGGTCT[C/T]CAACTCCTGGGCTCA | 6709 |
rs191513085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602406 | ATTTTTAGTAGAGAC[A/G]GGGTTTCGCCAAGTT | 6709 |
rs191519416 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558661 | AAAAGGCGTTAATCC[C/G]ATATGGCTGGGAACA | 6709 |
rs191522386 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579205 | TCTTTTTGCAATGAG[A/G]TAAGCTGATTCCAAA | 6709 |
rs191713922 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559986 | GTGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC | 6709 |
rs191761167 | snp | C/T | | | missense | SPTAN1 | GRCh38.p7 | 9:128583934 | AACCTCCAGAAGAAA[C/T]ATGCACTGCTAGAGG | 6709 |
rs191761343 | snp | A/G/T | 3.33424e-05 | 0.00408293 | missense | SPTAN1 | GRCh38.p7 | 9:128583227 | GAAGTGGCAGCTCGT[A/G/T]TGAATGAGGTGATCA | 6709 |
rs191771342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561758 | CCATATTCTGGGAAC[C/T]GGAGGATCCCAGGTC | 6709 |
rs191971169 | snp | A/T | 0.00319242 | 0.0398249 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608847 | GCCACAGGCCCACCT[A/T]GATCTCATGCCTTTG | 6709 |
rs191980199 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564344 | GAATTGCTTGAACCC[A/G]GGATGCAGAGGTTTC | 6709 |
rs192037681 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576174 | CAAGAACCCTGAAAT[C/G]CTTCATTTTATTACT | 6709 |
rs192041016 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128605457 | CTCCCACGACCTGCA[A/G]CGCTTCCTTAGCGAT | 6709 |
rs192070244 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567419 | GCCTCAGCCTCCCAG[A/G]TTGCTGGGATTACAG | 6709 |
rs192070654 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561429 | AGCTCTTTTGGAGGC[C/T]GAGGCAGGCAGATCA | 6709 |
rs192132955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612384 | CCTTATTATATATGA[A/G]TTGCATGCTGTAAGG | 6709 |
rs192147350 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128633047 | GGTAACAGGCCCTGC[A/G]CTGGGTATTCTCCCC | 6709 |
rs192148384 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591256 | CTTTTTTAGTAGAGA[C/T]GGGGTTTCACTGTGT | 6709 |
rs192243990 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562025 | TTATAAGATGAATGA[C/T]AGAGGTGGGTGGTCA | 6709 |
rs192292804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128556751 | AATGTGGTTTAAGCA[A/G]AAATATTTGTTGTTT | 6709 |
rs192303313 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606515 | GGGGGGAAGCGTTTC[A/G]CTTTTGTGCCCAGGC | 6709 |
rs192312974 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570535 | TAGAGATGGGGTTTC[A/G]TCATGTTGACCAGGC | 6709 |
rs192317563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588601 | CACGTATGAGCCACC[A/G]TGCCCAGACAAAATG | 6709 |
rs192376190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618735 | TGATCTGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 6709 |
rs192376464 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562570 | AACTGGAAGGTGACT[A/G]AGTGAAGTCTTGTTT | 6709 |
rs192387303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630256 | CTCTCTCTGAGAGAA[A/G]GTTCATTCTGAGCTC | 6709 |
rs192392431 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594496 | AGTGCAGTGGTATGA[C/G]TTCGGCTCACTGCAA | 6709 |
rs192569008 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591092 | TATGAGACAGAGTCT[C/T]GCTCTGACGCCCAGG | 6709 |
rs192577703 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566106 | TTGTCACCCAGGGCG[G/T]AGCGCAGTGGTGCAA | 6709 |
rs192634051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584941 | CACAAACCAGGCTCT[A/G]GGGCTGAATACCATC | 6709 |
rs192649200 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623524 | GCAGTGGCATGATCT[C/T]GGCTCACTGCAGCCT | 6709 |
rs192734104 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619375 | GAGGACAACAGAGAT[G/T]TATTGCTTCTCAGTT | 6709 |
rs192736333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571458 | AGCGTGGTGTTGCGT[A/G]CCTGTAATCCCAGCT | 6709 |
rs192854168 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601082 | TCTGCTTCCCAGATT[C/T]AAGCGATCCTCCTTC | 6709 |
rs192870506 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557624 | AATGAAAATTCCCCA[A/G]ATACCAAGAACTGCC | 6709 |
rs192948837 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594849 | TTTTTTCCTTTTGAG[A/G]CAGAGTCTCTCTTTT | 6709 |
rs193003386 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628549 | CAGGGAGGAGCAGGG[C/T]TGGGCTGTCCCGCCC | 6709 |
rs193019880 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586327 | TAGTAGAGACAGGGT[C/T]TCGCTATGTTGTCCC | 6709 |
rs193065306 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623126 | AGTGGCACGATCTCG[A/G]CTCACTGTAGCCTCT | 6709 |
rs193067321 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578358 | ATGTTATTCACAGGT[A/G]TTTCTCATCATGAGG | 6709 |
rs193111526 | snp | C/T | 1.64974e-05 | 0.00287201 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128580927 | TGCCCCCAAGCTGAC[C/T]GTCCTTTCCGAGGAG | 6709 |
rs193116500 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611579 | ACAAACTCCAATTGC[C/G]TTCTGTTAAAAACGT | 6709 |
rs193209273 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606949 | ATTCCTTAACTAATC[A/G]CCCCCTCTTCTCTCT | 6709 |
rs193268426 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602897 | CACTTTGGTCCCCCA[A/G]AGTGCTGGGATTACA | 6709 |
rs193270705 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631880 | CGTACTTGTCCTTGG[C/T]GTGCACTGCCCTCTG | 6709 |
rs193271808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559060 | GAAAATTCTGAATGC[C/T]GACTGCAGTGGGAGC | 6709 |
rs199532672 | snp | A/G | 0.00564116 | 0.0528087 | missense | SPTAN1 | GRCh38.p7 | 9:128618885 | GGGGTCAGCGGCTGG[A/G]AGAGTCCTTGGAATA | 6709 |
rs199561983 | snp | A/G | 0.00199804 | 0.031544 | missense, intron-variant | SPTAN1 | GRCh38.p7 | 9:128593021 | GCAGTGTATCTCTGC[A/G]TATGAAGCAGGTGGA | 6709 |
rs199569281 | snp | A/G | 3.30688e-05 | 0.00406612 | missense, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633326 | ACCCGCTCGCTTTTC[A/G]TGAACTGAGCCACTC | 6709 |
rs199588859 | snp | A/G | 4.96767e-05 | 0.00498356 | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633375 | CGCTGCTTGCCCTGC[A/G]TCGCCTTGCTGCATG | 6709 |
rs199588924 | snp | A/G/T | 8.73028e-05 | 0.00660645 | missense | SPTAN1 | GRCh38.p7 | 9:128604345 | TGAATGAGCGCTGGC[A/G/T]GTCCCTACAGCAGCT | 6709 |
rs199620607 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624914 | GGGCTGCAGGGAGCT[C/G]GTCATGGCACAGATG | 6709 |
rs199629769 | in-del | -/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599480 | AAGACAAAAAAAGTT[-/G]GGTTTTTTTTTTTTT | 6709 |
rs199660054 | snp | G/T | 3.30836e-05 | 0.00406702 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604987 | GTGTCCTGTAATCAA[G/T]GCAGTTGTACTTGGC | 6709 |
rs199707663 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589709 | GCCTCCCGAGCAGCT[A/G]GGACTACAGGTGCCT | 6709 |
rs199720383 | snp | A/G | 0.000214942 | 0.0103646 | missense | SPTAN1 | GRCh38.p7 | 9:128584432 | AAGCAGAAGCTGGCC[A/G]ATTCTCTGCGGTTGC | 6709 |
rs199728041 | in-del | -/AATT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624114 | AAAAAAAAAAAAAAG[-/AATT]CCTAAAAGTAGAATT | 6709 |
rs199733653 | snp | G/T | 0.00199804 | 0.031544 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578100 | AATGTCTTCCTTTGG[G/T]TTTCCCTAGGCTTCA | 6709 |
rs199777847 | snp | C/T | 0.00199802 | 0.0315439 | missense | SPTAN1 | GRCh38.p7 | 9:128576926 | GGCAGGGGAAGCTCT[C/T]TGGGGCAGCAGAAGT | 6709 |
rs199779269 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589279 | TGGTTCTTTTTTTTT[C/T]TTTTTCTTTTCTTTT | 6709 |
rs199794676 | snp | A/C/T | 3.29594e-05 | 0.00405941 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599036 | TGAGAAGGACTTAAA[A/C/T]CTTGGGAAGAATATC | 6709 |
rs199802986 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598391 | GTTATTATGGCTTTT[G/T]CTTTAAAGGACCTGA | 6709 |
rs199821592 | in-del | -/A | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623959 | TGGTGGTGTTCGCCT[-/A]TTAGTCCCAGCTACT | 6709 |
rs199833624 | snp | A/G | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128555301 | TCATGATTTTGTTCC[A/G]TTTGCCCTTAGAAGC | 6709 |
rs199839122 | snp | C/G | 0.000181475 | 0.00952389 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580909 | CCCTGACCATGTCTC[C/G]TATGCCCCCAAGCTG | 6709 |
rs199866550 | snp | A/G | 0.000198298 | 0.00995538 | missense, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633266 | AAGCCCTACGTGGAC[A/G]GCAAGGGCCGCGAGC | 6709 |
rs199866820 | in-del | -/TGAG | 0.0360663 | 0.129354 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569327 | CTGGGAGGGGTTTAC[-/TGAG]GTCTAGGCAGCAAGC | 6709 |
rs199902257 | snp | A/G | 0.00199792 | 0.0315431 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128605100 | CACAGACAATTATGG[A/G]CATGATCTCGCCAGT | 6709 |
rs199926005 | snp | C/T | 0.00199799 | 0.0315437 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626375 | ACTCCGCCAACTCAG[C/T]CTCTTCTGCTTCCAG | 6709 |
rs199930602 | snp | C/G | 0.000791687 | 0.0198801 | missense | SPTAN1 | GRCh38.p7 | 9:128626519 | CAAAGCTTTGCGCGA[C/G]GCCCACGACGCCTTC | 6709 |
rs199946535 | in-del | -/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615309 | TTAAGTGAAACAGCA[-/T]TTTTTTTTTCACTGT | 6709 |
rs199946916 | in-del | -/GTGTATGT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574970 | CCAGCTGCTCTCTAG[-/GTGTATGT]GCTATTCTGTAACTC | 6709 |
rs199955815 | snp | C/G | 0.00225926 | 0.0335434 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632518 | GCCCTGGCTGGGTGG[C/G]GGGTGTTCGGCAGCA | 6709 |
rs199973563 | snp | A/G | 0.00199802 | 0.0315439 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625981 | TCACTTCCGCAAGGT[A/G]AGGATGGGGCCACGT | 6709 |
rs199981833 | snp | A/C/T | 0.00166282 | 0.0287866 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607735 | GCTGAGTAGCAAAGA[A/C/T]GTGGCTGCTCTGCAG | 6709 |
rs199983545 | snp | A/G | 0.000181194 | 0.00951651 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591438 | ATTCTCCCTCTCAGA[A/G]AAGGAATTTACTTTC | 6709 |
rs199996370 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570330 | TATATATATATATAT[A/T]TTTTTTTTTTTTTTT | 6709 |
rs200002602 | in-del | -/AAATATATATATACATGTATGTGTAT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562970 | ACTCCGTCTAAAAAA[-/AAATATATATATACATGTATGTGTAT]ATATATATATATATA | 6709 |
rs200025488 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562715 | ATCATTAAATATTAC[A/T]AAACTTTGGGAGGCC | 6709 |
rs200128608 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603188 | TTGTTAAATTTAGGG[G/T]TTTTTTTTTTCCGGA | 6709 |
rs200128928 | in-del | -/C | 0.0498117 | 0.149749 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589294 | TTTTTCTTTTCTTTT[-/C]TTTTTTTTTTTTGAG | 6709 |
rs200130829 | snp | C/G/T | 4.95916e-05 | 0.00497933 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581107 | GAGAAGAAGGGCCTG[C/G/T]GTTTTGCCTCCTCGG | 6709 |
rs200155297 | snp | C/T | 6.60012e-05 | 0.00574423 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632550 | GGCTGCCTGCTGAGC[C/T]GCCCTCGGCTTTGTG | 6709 |
rs200180598 | snp | C/T | 0.000329495 | 0.0128312 | SPTAN1 | 9 | allele_origin=T(germline)/C(germline) | 9:128607929 | GCAGCTGTTGGCTCA[C/T]GGACACTATGCCAGC | 6709 |
rs200241514 | snp | G/T | 1.65061e-05 | 0.00287277 | missense | SPTAN1 | GRCh38.p7 | 9:128584309 | GGCATCACCATTCAG[G/T]CCCGCCAGTTCCAAG | 6709 |
rs200243332 | snp | C/G/T | 3.29453e-05 | 0.00405854 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128577180 | GGAGCAGTTAATGGC[C/G/T]TCTGATGATTTTGGC | 6709 |
rs200248814 | snp | A/G | 0.000296482 | 0.0121718 | missense | SPTAN1 | GRCh38.p7 | 9:128618918 | AGCAGTTTGTAGCCA[A/G]TGTGGAAGAGGAAGA | 6709 |
rs200321068 | in-del | -/GA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606499 | ATATTTTTTTTTTGG[-/GA]GGGGGGAAGCGTTTC | 6709 |
rs200338619 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572330 | TTCCACATGTTTATG[A/G]AGTGCACCTGCCTCC | 6709 |
rs200372004 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627863 | TTCTCTCTGTCCCCC[C/T]GATTGCTGCTGTTGT | 6709 |
rs200399458 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631677 | CTAAAAATACAAAAA[G/T]TAGGCAGGTGTGGTG | 6709 |
rs200409125 | snp | C/T | 0.00199802 | 0.0315439 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567011 | GATTCCTGCCAAAAT[C/T]CAAGAGCCCAAATGT | 6709 |
rs200409897 | snp | A/G | 1.65811e-05 | 0.00287929 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575358 | CAGGTAAATAGCAAA[A/G]TGCTGTATGCTTCTC | 6709 |
rs200434729 | snp | C/G | 2.93638e-05 | 0.00383159 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593079 | CAGAGCACCAATGTC[C/G]ACTGCTACCCTATCC | 6709 |
rs200456378 | snp | A/G | 0.00102334 | 0.0225969 | SPTAN1 | 9 | allele_origin=G(germline)/A(germline) | 9:128632713 | GGACACGGTGGATCC[A/G]AACAGGTAAATTAAT | 6709 |
rs200468422 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565124 | CCTGGCCAACATGGT[A/G]AAACCCCATCTCTAC | 6709 |
rs200471801 | snp | A/T | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128553406 | CTCAAATCAAATAAC[A/T]TAATAGCTTAGCGTT | 6709 |
rs200475859 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584615 | AGGATGGGCAGGGTC[A/G]AATTTAAATTATTGA | 6709 |
rs200476822 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561580 | AGGCAGGAGAATGGC[A/T]TGAACCGGGGAGGCG | 6709 |
rs200500840 | snp | A/G | 1.68462e-05 | 0.00290221 | downstream-variant-500B, missense | SPTAN1, WDR34 | GRCh38.p7 | 9:128633766 | GCCACCTCTGCTGCC[A/G]GGCAGTCCAGGTCCT | 6709 |
rs200531434 | snp | A/G | 4.95765e-05 | 0.00497853 | missense, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633278 | GACGGCAAGGGCCGC[A/G]AGCTCCCCACCGCGT | 6709 |
rs200543425 | snp | G/T | 0.00266886 | 0.0364322 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605029 | TGAATGTGTCTCGCC[G/T]TTAGAGATGCTGATG | 6709 |
rs200580276 | snp | C/G | 5.30645e-05 | 0.00515067 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593064 | AGGCTGAGAGTCTTG[C/G]AGAGCACCAATGTCC | 6709 |
rs200590385 | snp | C/T | 0.000296609 | 0.0121744 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598925 | GAGAGATGTGTATTT[C/T]TTCTAATAATAAAAC | 6709 |
rs200597008 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589285 | TTTTTTTTTCTTTTT[C/T]TTTTCTTTTTTTTTT | 6709 |
rs200641770 | snp | A/G | 9.88631e-05 | 0.00703006 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128615784 | AGCCAAGCTGAATGA[A/G]TCCCATCGCCTGCAC | 6709 |
rs200666012 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562717 | CATTAAATATTACAA[A/C]ACTTTGGGAGGCCAA | 6709 |
rs200685538 | snp | C/T | 4.94173e-05 | 0.00497053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603496 | GCTCAGATCTCTAAT[C/T]GCCAGACACTTGATT | 6709 |
rs200699396 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601564 | CCGGCTCTACAAATA[A/C]AAATAAAAATGTTTT | 6709 |
rs200702768 | snp | C/G | 0.000767218 | 0.0195709 | downstream-variant-500B, missense | SPTAN1, WDR34 | GRCh38.p7 | 9:128633930 | CTGGGTTTGCTTGAT[C/G]AAAACTGTGGGTTTC | 6709 |
rs200711426 | snp | A/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128579730 | GCCTCAGATGAAGTG[A/G]GGGAGAAGGTAAGAG | 6709 |
rs200725239 | in-del | -/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606497 | ATATATTTTTTTTTT[-/T]GGGGGGGGAAGCGTT | 6709 |
rs200728087 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584876 | GTGACATGGCTTGGT[G/T]CTGCTCCTCGTGTCT | 6709 |
rs200728908 | snp | A/C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558092 | ACAGGCGTGAGCCAC[A/C/T]GCGCCCAGCTGTATA | 6709 |
rs200732747 | snp | A/G | 0.00199792 | 0.0315431 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604994 | GTAATCAAGGCAGTT[A/G]TACTTGGCATTTCTT | 6709 |
rs200733545 | in-del | -/A | 0.0337553 | 0.125452 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625012 | GATTTATCTGTACAC[-/A]AAAAAATGGTTTGTC | 6709 |
rs200736013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633153 | GAGACCTGGGAGGTC[A/G]GGTTTGAAGTGGGTG | 6709 |
rs200749390 | snp | G/T | 0.000132474 | 0.00813755 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608321 | CTGGATTTTTCCTGA[G/T]TGACATCTGTTTCTT | 6709 |
rs200751769 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572477 | GGCCTTGCCCTAGTT[C/T]TTTCTTGAGGGTGTA | 6709 |
rs200798924 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582329 | CTCAAAAGTTATGAG[A/G]AAAAATGTCATCACC | 6709 |
rs200827350 | snp | C/T | 0.00199791 | 0.0315431 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128580955 | GAGAGAGCGGCGCTG[C/T]TGGAGCTGTGGGAGC | 6709 |
rs200834733 | snp | A/G | 1.73441e-05 | 0.00294478 | missense | SPTAN1 | GRCh38.p7 | 9:128626608 | AGATCAAGAGCTTCC[A/G]CGTAGCCTCCAACCC | 6709 |
rs200844958 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602065 | AGGTACCTTTATAAA[C/T]CCCAGTACCTCTTAT | 6709 |
rs200872929 | snp | C/T | 0.000399281 | 0.0141238 | missense, intron-variant | SPTAN1 | GRCh38.p7 | 9:128592987 | CCTCTGTGCAGGACA[C/T]GCATAACTAAGGAGG | 6709 |
rs200948972 | snp | A/G | 8.24287e-05 | 0.00641931 | missense | SPTAN1 | GRCh38.p7 | 9:128581016 | ACCTGCAGCTCTTCT[A/G]CCGGGACACTGAGCA | 6709 |
rs200959763 | snp | A/G | 0.00488448 | 0.049177 | SPTAN1 | 9 | allele_origin=G(germline)/A(germline) | 9:128611865 | GGCCCACCAGCTCCC[A/G]GTGCCCAGGGAGGAA | 6709 |
rs200973042 | snp | C/G | 1.64917e-05 | 0.00287151 | missense | SPTAN1 | GRCh38.p7 | 9:128581891 | AGGAGGAAAAGATTA[C/G]AGTAAGACCCCTTCT | 6709 |
rs200978151 | snp | C/T | 0.00013202 | 0.00812357 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574656 | TGATCTGATTAAAAC[C/T]CTGATTTGAAACTTT | 6709 |
rs201020114 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589282 | TTCTTTTTTTTTCTT[C/T]TTCTTTTCTTTTTTT | 6709 |
rs201064387 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560634 | GATCTGCCCGCCTCG[C/G]CTCCCAAAGTATTGG | 6709 |
rs201080196 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620725 | CTCCGTCTCAAAAAG[A/G]AAAAAAAAAGACATG | 6709 |
rs201100247 | snp | A/G | 4.9498e-05 | 0.00497459 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632557 | TGCTGAGCCGCCCTC[A/G]GCTTTGTGCTGCAGA | 6709 |
rs201100676 | in-del | -/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128556301 | GTCGGACCTTTTTCA[-/C]AAAAAAAAAATTTAG | 6709 |
rs201136631 | snp | A/G | 0.000399281 | 0.0141238 | missense | SPTAN1 | GRCh38.p7 | 9:128600080 | TCTTTCTTTGAATAG[A/G]ATGAAACTGATTCCA | 6709 |
rs201168391 | snp | A/G | 3.29506e-05 | 0.00405884 | missense | SPTAN1 | GRCh38.p7 | 9:128582734 | ACGAGAGAGCCATGC[A/G]TCGCCGGGCCCAGCT | 6709 |
rs201203115 | snp | A/G | 0.00199806 | 0.0315443 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128594310 | CGCTCTGACAAGTGA[A/G]GAGGTCGGAGCAGAC | 6709 |
rs201203777 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606373 | GAGCAAGACTCTGCC[C/T]CAAAAAAAAAAAAAA | 6709 |
rs201215315 | in-del | -/A | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606488 | TATATATATATATAT[-/A]TTTTTTTTTGGGGGG | 6709 |
rs201249013 | snp | C/T | 0.000131791 | 0.00811655 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128574791 | ACGAGAATGTGAGGA[C/T]GTGATGGACTGGATC | 6709 |
rs201268986 | snp | C/T | 0.0029955 | 0.0385847 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626332 | GCACCCCACCTCCTG[C/T]ACTGCGTCGGCACGT | 6709 |
rs201272649 | in-del | -/CTCACACCTGTAAT | 0.00874735 | 0.0655527 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601460 | GGCTAGGTGTTGTGG[-/CTCACACCTGTAAT]CCCAGCATTGTGGGA | 6709 |
rs201319189 | snp | A/G | 0.000148247 | 0.00860822 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584706 | GGATAACTGGGGACT[A/G]GTGTCTGCTTTCAGG | 6709 |
rs201329295 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624113 | AAAAAAAAAAAAAAA[C/T]AATTCCTAAAAGTAG | 6709 |
rs201330555 | snp | G/T | | | missense | SPTAN1 | GRCh38.p7 | 9:128626587 | AGCTGGCCGAGCTGG[G/T]CCGCCAGATCAAGAG | 6709 |
rs201330964 | snp | A/G | | | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128579726 | CTATGCCTCAGATGA[A/G]GTGAGGGAGAAGGTA | 6709 |
rs201336861 | snp | A/G | 0.000124408 | 0.00788597 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588993 | CGCTGGCACCTCCAC[A/G]TATGCTCAGTTGGGT | 6709 |
rs201348060 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578835 | TCACTCTGTCTCAAA[A/G]AAAAAAAAAAAAAAA | 6709 |
rs201348505 | snp | C/T | 0.000434754 | 0.0147373 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632931 | AGAGGGAAAGCCTTA[C/T]GTGACCAAGGAGGAG | 6709 |
rs201348797 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623955 | TGCATGGTGGTGTTC[A/G]CCTATTAGTCCCAGC | 6709 |
rs201363088 | snp | A/G/T | 1.69324e-05 | 0.00290962 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615866 | TCAGCCCTCTAGAAG[A/G/T]CCCCTTACGCCTGTA | 6709 |
rs201371607 | in-del | -/T | 0.0142736 | 0.0832652 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569361 | TTAAAGCTCCAGCTC[-/T]AAGGAATGATGTGTG | 6709 |
rs201411901 | snp | A/G | 0.000988386 | 0.0222085 | missense | SPTAN1 | GRCh38.p7 | 9:128625889 | ATCGAGGCCCGGCAC[A/G]CCTCCCTCATGAAGA | 6709 |
rs201450015 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581604 | TCATGATATGGCTGG[A/G]TTGATTTTAAGAAAA | 6709 |
rs201463905 | snp | A/G | 0.000488162 | 0.0156155 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585985 | CCAGGCGTGGGAAGC[A/G]TCTCACCTGCCAGGG | 6709 |
rs201555611 | snp | C/T | 4.94173e-05 | 0.00497053 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128581847 | GCTTCTTAAGAAGCA[C/T]GAAGACTTTGAGAAA | 6709 |
rs201561438 | snp | C/T | 0.000132004 | 0.0081231 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632537 | TGTTCGGCAGCAGGG[C/T]TGCCTGCTGAGCCGC | 6709 |
rs201566226 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | SPTAN1, WDR34 | GRCh38.p7 | 9:128633743 | CGCCTCCCGGGACCC[C/T]TCAGGCCGCCACCTC | 6709 |
rs201587446 | snp | A/T | 1.64931e-05 | 0.00287163 | missense | SPTAN1 | GRCh38.p7 | 9:128609269 | TGAGTCGTACAAGGA[A/T]CCCACCAACATCCAG | 6709 |
rs201598809 | in-del | -/GAT | | | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128550882 | TTTCTCTACATAGAA[-/GAT]TGCAGGAAATGCCTC | 6709 |
rs201641556 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562714 | TATCATTAAATATTA[C/T]AAAACTTTGGGAGGC | 6709 |
rs201645927 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576123 | TTGAGCTTGAGAAAA[A/G]TAGTCAGGCCAAACC | 6709 |
rs201693154 | snp | A/G | 0.000399281 | 0.0141238 | missense | SPTAN1 | GRCh38.p7 | 9:128632128 | CCCCACCCCTGCAGC[A/G]CAAGCACCAGGAAAT | 6709 |
rs201716851 | snp | A/G | 6.59848e-05 | 0.00574352 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128608264 | AGACTTTGACAAAGC[A/G]ATTAACGTCCAGGTG | 6709 |
rs201755611 | snp | C/T | 0.000115307 | 0.00759211 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608116 | TTTTCTCACCTGCCT[C/T]TTGCCCTCTTTAGCT | 6709 |
rs201757065 | snp | G/T | 0.000181826 | 0.00953309 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581106 | GGAGAAGAAGGGCCT[G/T]TGTTTTGCCTCCTCG | 6709 |
rs201763197 | snp | G/T | 1.65108e-05 | 0.00287317 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574639 | TCCCACAGAGCCAGT[G/T]GTGATCTGATTAAAA | 6709 |
rs201796563 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577886 | AATGTGGGACAGGAT[A/C]GGGGCATTATAGTGA | 6709 |
rs201804053 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561689 | AAAAAAAAAAAAAAA[C/T]AATATGTCAATATGT | 6709 |
rs201923046 | snp | A/G | 4.94645e-05 | 0.00497291 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607811 | GACGTCAGAGTGGGC[A/G]TCTGCTGCCAGTTAC | 6709 |
rs201947293 | snp | A/G/T | 0.000133776 | 0.0081775 | missense | SPTAN1 | GRCh38.p7 | 9:128577494 | GACATGCACGGCTCA[A/G/T]TGATTCATACAGGTG | 6709 |
rs201948749 | snp | A/G | 0.00011541 | 0.00759549 | missense | SPTAN1 | GRCh38.p7 | 9:128580974 | AGCTGTGGGAGCTGC[A/G]CAGGCAGCAGTACGA | 6709 |
rs201981160 | in-del | -/AC | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626779 | CTGAGTCACGACAAG[-/AC]ACGAGCAGGATGGAG | 6709 |
rs201988969 | snp | C/G/T | 6.90536e-05 | 0.00587555 | downstream-variant-500B, intron-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128634002 | AAAGAGAGACAGATA[C/G/T]GTGGAGTAAGAGAAA | 6709 |
rs201997683 | snp | A/G | 8.24858e-05 | 0.00642153 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574860 | CTTTACTCAAAGAAA[A/G]GGGAAGAGACTCCTC | 6709 |
rs202015283 | snp | C/G | 0.00159798 | 0.0282212 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617951 | GAAGCACCAGAAGAG[C/G]TACCTGCTGTTAACC | 6709 |
rs202041478 | snp | A/G | 0.000379961 | 0.0137781 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605003 | GCAGTTGTACTTGGC[A/G]TTTCTTAACCTGAAT | 6709 |
rs202050820 | in-del | -/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590554 | ATTTATATTAAAAAA[-/G]AAAAAAAAAAAAAAG | 6709 |
rs202081762 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128555625 | TTTGCAAAGCCTTTT[C/T]TTTTTTTTTTTTTTT | 6709 |
rs202099793 | snp | C/T | 1.6483e-05 | 0.00287076 | missense | SPTAN1 | GRCh38.p7 | 9:128577394 | CGCCTGCAACAGTCC[C/T]ACCCTCTGAGTGCAA | 6709 |
rs202115736 | snp | A/G | 0.00199792 | 0.0315431 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128566767 | TGGGGTCAAAGTGCT[A/G]GAAACAGCAGAGGAC | 6709 |
rs202120121 | in-del | -/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606496 | TATATATTTTTTTTT[-/G]TGGGGGGGGAAGCGT | 6709 |
rs202129574 | snp | C/T | 3.29451e-05 | 0.00405851 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128591500 | GAAAGTGGAAGTGAA[C/T]GATCGTCAGGGTTTT | 6709 |
rs202149029 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572778 | CACCATACCGGACAG[C/T]GTGGCGCCCCATAGT | 6709 |
rs202161153 | snp | C/G | 0.00299544 | 0.0385843 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608858 | ACCTTGATCTCATGC[C/G]TTTGTTTTCTGACAG | 6709 |
rs202180736 | snp | A/G | 0.000198383 | 0.00995752 | SPTAN1 | 9 | allele_origin=G(germline)/A(germline) | 9:128632800 | GCTCTTGCTTCCCCC[A/G]CTCCTAGAGATGGCC | 6709 |
rs202188303 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564600 | AAATAAATAAATAAA[A/T]ATCTGGTATACAAAT | 6709 |
rs202200323 | snp | A/C | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128553405 | GCTCAAATCAAATAA[A/C]TTAATAGCTTAGCGT | 6709 |
rs202220208 | snp | A/G | 6.65901e-05 | 0.0057698 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621129 | CATAGCAGGCTCTCA[A/G]TAGTGTGCCTTGGCT | 6709 |
rs202239487 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631818 | GTGAGACTCCATCTC[G/T]AAAAAATTTATAAAA | 6709 |
rs267602137 | snp | C/T | | | missense | SPTAN1 | GRCh38.p7 | 9:128621212 | ACCGTCCACAAGGAT[C/T]GCGTGAATGATGTCT | 6709 |
rs367605322 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631998 | CCACTATTCCTATTC[C/T]AGAATGTTCTTGTTT | 6709 |
rs367614873 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622275 | GTGTCCTTCAGCCTC[C/T]TGGCAACGAGCCAGC | 6709 |
rs367629442 | snp | C/G | 1.64803e-05 | 0.00287052 | missense | SPTAN1 | GRCh38.p7 | 9:128625888 | CATCGAGGCCCGGCA[C/G]GCCTCCCTCATGAAG | 6709 |
rs367630152 | snp | A/G | 0.000364806 | 0.0135007 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591660 | CCGCAAGGGCTAGGC[A/G]TCCCATAGGCATACT | 6709 |
rs367635991 | snp | A/G | 1.64773e-05 | 0.00287026 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128607902 | TTTCCAGGCATTTGA[A/G]CAGTTTGGACAGCAG | 6709 |
rs367637995 | snp | A/G | 1.65806e-05 | 0.00287924 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582877 | TAGTGTTGCCATGTA[A/G]CACTCGATTAGTAAG | 6709 |
rs367654110 | snp | A/G | 6.71276e-05 | 0.00579304 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630199 | GGCCAGTTGCAGTTA[A/G]GTTTGGTTTCCTTAA | 6709 |
rs367678277 | snp | A/G/T | 0.000130215 | 0.00806799 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593057 | TGTGAGTAGGCTGAG[A/G/T]GTCTTGCAGAGCACC | 6709 |
rs367686263 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128584770 | GAAACATCAAGCCTT[A/G]CAAGCAGAAATTGCT | 6709 |
rs367687143 | snp | C/T | 3.30349e-05 | 0.00406403 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568763 | GCTCACTTCAAGGTC[C/T]GCCAACAGGGAAAGC | 6709 |
rs367696535 | snp | A/G | 1.67536e-05 | 0.00289423 | intron-variant, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633160 | GGGAGGTCGGGTTTG[A/G]AGTGGGTGCAGCTGG | 6709 |
rs367706466 | snp | A/C/T | 0.000115347 | 0.00759358 | SPTAN1 | 9 | allele_origin=A(germline)/C(germline) | 9:128630385 | ACCAAAGTAAGTGCC[A/C/T]GTGGGGCTCTGGCCC | 6709 |
rs367718622 | snp | C/G | 4.94238e-05 | 0.00497086 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578106 | TTCCTTTGGTTTTCC[C/G]TAGGCTTCAACGCTT | 6709 |
rs367737604 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591077 | TGGACCTTTTTTTTT[A/T]ATGAGACAGAGTCTC | 6709 |
rs367760545 | snp | A/G | 0.000911011 | 0.0213231 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584016 | GTGAATGCAGAAACT[A/G]TAGGAGGGAGGAAAA | 6709 |
rs367772623 | snp | C/T | 0.000610828 | 0.0174654 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128608918 | TGCCGACCAGCTCAT[C/T]GCTGCCGGCCATTAT | 6709 |
rs367776636 | snp | A/C/G | 0.00033045 | 0.0128499 | missense, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633296 | CTCCCCACCGCGTTC[A/C/G]ACTACGTGGAGTTCA | 6709 |
rs367832791 | snp | G/T | 0.000461141 | 0.0151775 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577112 | GCTGTGGATTAACTG[G/T]TGCCTTTGTTCTGTA | 6709 |
rs367863141 | snp | A/G | 0.000137514 | 0.00829084 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611683 | AACCTAGCAGGAACT[A/G]GTTTGGAAAAAATTT | 6709 |
rs367870535 | snp | C/T | 4.94173e-05 | 0.00497053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627963 | TATTGTTTTCTTCCT[C/T]CTCTGGGCTTGTCAT | 6709 |
rs367875946 | snp | A/G | 1.66214e-05 | 0.00288278 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591669 | CTAGGCGTCCCATAG[A/G]CATACTCTGTTCCAC | 6709 |
rs367910307 | in-del | -/GCTGGGAACAGCCTGGAA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558667 | CGTTAATCCCATATG[-/GCTGGGAACAGCCTGGAA]CGTTCTCTGTGAAGT | 6709 |
rs367925255 | snp | A/T | 1.65059e-05 | 0.00287275 | missense | SPTAN1 | GRCh38.p7 | 9:128584326 | CCGCCAGTTCCAAGA[A/T]GCTGGCCATTTTGAT | 6709 |
rs367979122 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591810 | CTGACTGATGACTTA[C/T]ATTGCTTTGTTTTTT | 6709 |
rs367989148 | snp | C/T | 0.000364238 | 0.0134902 | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633380 | CTTGCCCTGCGTCGC[C/T]TTGCTGCATGTCCGC | 6709 |
rs368047576 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562813 | ACTAAAAAATAGAAA[A/G]TATTAGCCGGGCGTG | 6709 |
rs368100790 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583533 | CATTGCTGAAAATCA[A/G]AGTTCAGCTGAGAGC | 6709 |
rs368131682 | snp | A/G | 1.66696e-05 | 0.00288696 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621120 | CCCACAACACATAGC[A/G]GGCTCTCAATAGTGT | 6709 |
rs368309008 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570528 | TATTTAGTAGAGATG[C/G]GGTTTCATCATGTTG | 6709 |
rs368313840 | snp | C/T | 3.29457e-05 | 0.00405854 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603621 | CAGCTCCTCTGATCT[C/T]CCCTGGTTTTCTCCA | 6709 |
rs368321814 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128578185 | CCTCATCAATGCAGA[C/T]GAGCTTGCCAGTGAT | 6709 |
rs368329742 | snp | A/C/T | 6.60342e-05 | 0.00574573 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632502 | GAGTTCAGCCTTACT[A/C/T]GCCCTGGCTGGGTGG | 6709 |
rs368330278 | snp | A/C | 1.64969e-05 | 0.00287196 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583779 | AATTAAACTTGTTTT[A/C]TTCCATAGGAATAAA | 6709 |
rs368348802 | snp | A/C | 0.000646825 | 0.017972 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581927 | GTGCTTTCAAATGAC[A/C]CTTATAGTAAGCCAG | 6709 |
rs368402085 | snp | C/T | 1.64768e-05 | 0.00287021 | missense | SPTAN1 | GRCh38.p7 | 9:128615759 | TCAAGAGCATGGCGG[C/T]CTCCCGGCGAGCCAA | 6709 |
rs368406599 | snp | A/G | 1.64833e-05 | 0.00287078 | missense | SPTAN1 | GRCh38.p7 | 9:128591604 | GCAGCATAGCACTGC[A/G]GCAGGAGCAGATTGA | 6709 |
rs368470565 | snp | C/T | 6.62241e-05 | 0.00575392 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566720 | TGGTACTTATCTCAG[C/T]GCATTTTGTCATTTC | 6709 |
rs368482631 | snp | A/G | 1.65168e-05 | 0.00287369 | missense | SPTAN1 | GRCh38.p7 | 9:128566871 | AGCTGGAAGATTCCT[A/G]TCGATTCCAGTTCTT | 6709 |
rs368483063 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610331 | GGATTTGAACCAAAG[A/G]GTGATCAGAACAAGG | 6709 |
rs368517483 | snp | A/C | 0.000153988 | 0.00877328 | missense | SPTAN1 | GRCh38.p7 | 9:128605419 | GGGAAACGTGCAGAT[A/C]AGCGCAAGGCAAAGT | 6709 |
rs368533485 | snp | A/G | 9.88647e-05 | 0.00703012 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607564 | AAGATCTCCTTACCA[A/G]GTAATATAATAGCTA | 6709 |
rs368551564 | snp | A/G | 3.3151e-05 | 0.00407117 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584232 | TTTTTCTCTGTATAC[A/G]ATAAAACCACACCCA | 6709 |
rs368584313 | in-del | -/ATCACACATGA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618371 | ATGAATCACACATGA[-/ATCACACATGA]TTCTCCAGAAATCAA | 6709 |
rs368586914 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571144 | AAAATTTAAAAATTA[A/G]TGGGGCGTGGTGGTG | 6709 |
rs368593108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605813 | CCTGGCCAACATGGC[A/G]AAATGCCGTCTCTAC | 6709 |
rs368596995 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568704 | GGGGAGGAACACGGG[C/G]AACAGCGGGGACAAA | 6709 |
rs368627372 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559782 | TTTCGTCGCCCAGGC[C/T]AGAGTGCAGTGGTGC | 6709 |
rs368690134 | snp | C/G/T | 3.34645e-05 | 0.0040904 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566986 | CTTGCAGGTACGTCT[C/G/T]ATCTCCTGGGATTCC | 6709 |
rs368739408 | in-del | -/TC | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557798 | ATTAAATTAGAAATT[-/TC]TTTTTTTTTTTTTTT | 6709 |
rs368776146 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586887 | CAGTGGCATGATCTC[A/G]GATAACTGCAACCTC | 6709 |
rs368786971 | snp | C/T | 0.00904082 | 0.0666234 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128555350 | CCCTCCCTCTTTAGA[C/T]TCCACATTCCTCCAT | 6709 |
rs368814792 | snp | A/C | 0.000131963 | 0.00812183 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594156 | TTGTCCCTCTTGTCA[A/C]CCTCTTGAATTCCAT | 6709 |
rs368833096 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625534 | CAGAGCTGGCAGGGA[C/T]CCCTGGGGCGGGAGA | 6709 |
rs368864898 | snp | A/G | 8.37149e-05 | 0.00646919 | downstream-variant-500B, missense | SPTAN1, WDR34 | GRCh38.p7 | 9:128633791 | GGTCCTCAGCTTCCC[A/G]GGGCCCTTGTTCCGT | 6709 |
rs368867002 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622119 | CTTTTCTTCCTTGCT[C/G]TGATCTGCAAATAAA | 6709 |
rs368876195 | snp | C/T | 1.65375e-05 | 0.0028755 | missense | SPTAN1 | GRCh38.p7 | 9:128579701 | GACAGGCACTGCTTG[C/T]TGCTGGTCACTATGC | 6709 |
rs368903432 | snp | A/G | 6.6346e-05 | 0.00575922 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626346 | GCACTGCGTCGGCAC[A/G]TCCAGCCCTGGCGAC | 6709 |
rs368931647 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575838 | ACAACCCTTCCCCAG[A/T]GCCCACGTGTACAAT | 6709 |
rs368949860 | snp | A/G | 1.64942e-05 | 0.00287173 | missense | SPTAN1 | GRCh38.p7 | 9:128615824 | CGGGACATGGATGAC[A/G]AGGAGTCCTGGATCA | 6709 |
rs368986406 | snp | C/G | 1.66142e-05 | 0.00288216 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582440 | CCAAGCTTGGGACTA[C/G]TGTGCTTACCAATGA | 6709 |
rs369002707 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581435 | CTATGATCGTACCAC[C/T]GCACTCTAGCCTGTG | 6709 |
rs369036039 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610691 | ATTTCAGTACCTTCT[A/G]TTTCTTTATGGATTC | 6709 |
rs369069640 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607005 | CTGCTTTCTATGTCT[A/G]TGGATTTGCCTCTTC | 6709 |
rs369081760 | snp | A/C/G | 0.000232522 | 0.0107802 | downstream-variant-500B, utr-variant-3-prime | SPTAN1, WDR34 | GRCh38.p7 | 9:128633707 | AGAAACACAAGGCTC[A/C/G]GCACAGCGAAGGCTT | 6709 |
rs369106919 | snp | A/C/T | 5.01772e-05 | 0.00500864 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585975 | GCTGAGGTAACCAGG[A/C/T]GTGGGAAGCGTCTCA | 6709 |
rs369108363 | snp | C/G | 4.59802e-05 | 0.00479458 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604432 | GGTGAGGGGTCAGCC[C/G]TGGGCTGGGAGAGGG | 6709 |
rs369187088 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564248 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 6709 |
rs369248888 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603271 | GTATTTTTCTGTCCA[A/G]CTAGCTGCTAGAATT | 6709 |
rs369283624 | snp | C/G | 0.000105893 | 0.00727566 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627371 | GCACAGCATCTGCCC[C/G]CCTTTGGCCCTCAGG | 6709 |
rs369311209 | in-del | -/CAAAAAAAAAA | 0.02016 | 0.0983543 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614589 | AATGAGACTACGTCT[-/CAAAAAAAAAA]CAAAAAAAAAACACA | 6709 |
rs369353631 | snp | A/G | 0.00069187 | 0.0185865 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582596 | CCTCCTTTTTGGTAC[A/G]TGAATGTCTCTTCTA | 6709 |
rs369370023 | snp | A/G | 1.64732e-05 | 0.0028699 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612293 | GGGGGATTTCTAGTC[A/G]TTTGGCACAGTGGGT | 6709 |
rs369402864 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596560 | GGATTACAGGCGTGA[A/G]CCACCACGCCCGGCC | 6709 |
rs369412335 | snp | A/C | 6.58903e-05 | 0.00573941 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584679 | TCAGTGCTGACTTTT[A/C]TCTTCATGGTTGGAT | 6709 |
rs369452745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587467 | GAAAATGATATTAGC[A/G]CTGTAAGAAGGGCAG | 6709 |
rs369456354 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598198 | GGTGATCCGCCCACT[A/T]GGGCCTCCCAAAGTG | 6709 |
rs369480626 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581608 | GATATGGCTGGATTG[A/G]TTTTAAGAAAATCCA | 6709 |
rs369508829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564621 | GTATACAAATATTAG[A/G]TTGCTCGGTGTAATC | 6709 |
rs369531936 | snp | C/T | 0.000100432 | 0.00708561 | synonymous-codon, intron-variant | SPTAN1 | GRCh38.p7 | 9:128593004 | CATAACTAAGGAGGC[C/T]GGCAGTGTATCTCTG | 6709 |
rs369536703 | snp | A/G | 1.64749e-05 | 0.00287005 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600046 | GTTTCATGGTCAATT[A/G]CTTGGCTGCCTAAAT | 6709 |
rs369538623 | snp | A/G | 0.000307953 | 0.0124049 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609016 | TAGTCACCAGCCCTG[A/G]GAGGATGCATCCCCT | 6709 |
rs369543563 | snp | C/T | 8.24355e-05 | 0.00641957 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625056 | TTTTCCTTTCTAATC[C/T]ATCTCCACTGAGGAG | 6709 |
rs369543961 | snp | A/G | 0.000144112 | 0.00848734 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621306 | CACTGGGACACCCAC[A/G]TGTTGGTACCACAGA | 6709 |
rs369547180 | snp | A/C/G | 1.65007e-05 | 0.00287229 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580906 | TCTCCCTGACCATGT[A/C/G]TCCTATGCCCCCAAG | 6709 |
rs369549261 | snp | A/G | 4.98062e-05 | 0.00499005 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587576 | GGCTTCAGCCCCTGC[A/G]CAGTGCTCCATGTGT | 6709 |
rs369571747 | snp | C/T | 1.65244e-05 | 0.00287436 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626378 | CCGCCAACTCAGTCT[C/T]TTCTGCTTCCAGGTG | 6709 |
rs369611161 | snp | A/G | 8.23676e-05 | 0.00641693 | missense | SPTAN1 | GRCh38.p7 | 9:128594207 | AACTGGGTGAGAAGC[A/G]TAAAGGCATGTTGGA | 6709 |
rs369615023 | snp | C/T | 4.98442e-05 | 0.00499196 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617773 | CAGGTAAGGAGGCCG[C/T]CTTCTGGCCAAGAGG | 6709 |
rs369617693 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578892 | CTAGATACAAAATCA[A/G]TATACTGAAAGTCAA | 6709 |
rs369663978 | snp | C/T | 0.000115845 | 0.00760981 | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633360 | GGGTCACCCACCCCT[C/T]GCTGCTTGCCCTGCG | 6709 |
rs369670539 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128613428 | CAAAGACCTAGCTTC[C/T]GTGAACAACCTGCTG | 6709 |
rs369670645 | snp | A/G | 0.000307953 | 0.0124049 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568927 | CTCGTGGAGTGGATG[A/G]CTTCATCTGGGTGGA | 6709 |
rs369671684 | snp | C/G | | | downstream-variant-500B, intron-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128634100 | AGTGGCTTTGAGTTG[C/G]GTTGCTGGAGGGAAG | 6709 |
rs369710857 | snp | A/G | 6.59174e-05 | 0.00574059 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128583885 | AGGTCACTTGGCTTC[A/G]GATGATTACGGCAAA | 6709 |
rs369731494 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595336 | CCTGGTCTTGAACTC[C/G]TGGCCTCAAGTGATC | 6709 |
rs369747612 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128553046 | GGTGGGTGGGGGCTC[C/T]CTCGTCGGGATCTTC | 6709 |
rs369769925 | in-del | -/GA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594428 | AGATTTGAGTCTCTT[-/GA]TTTTTTTTTTTTTTT | 6709 |
rs369772583 | snp | C/T | 1.66076e-05 | 0.00288158 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585730 | TTTTGTTATCCTCTT[C/T]CCCTACCCATCTTCC | 6709 |
rs369773602 | snp | A/G | 1.67295e-05 | 0.00289214 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587710 | CCGGGTAAACTTGTA[A/G]CAGTTTATGGGTTAC | 6709 |
rs369789806 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128607995 | GGAGCGTGCAGACCT[A/G]GAGAAGGCCTGGGTT | 6709 |
rs369792563 | snp | C/G/T | 8.25076e-05 | 0.00642238 | missense, synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632686 | ACCTGACCCTGAGTT[C/G/T]GAGGCAATCCTGGAC | 6709 |
rs369842319 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560649 | CCTCCCAAAGTATTG[A/G]GATTACAGGTGTGAG | 6709 |
rs369870029 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617318 | TTGATATATTAATAC[A/G]TATTTAGTATACATG | 6709 |
rs369911727 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564071 | TTGAGCCCAGGAGTT[C/G]AAGACCAGCCTAGGC | 6709 |
rs370055104 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128551547 | CCTGGGCCAAGAGAC[G/T]TAGCCTACATGAGCA | 6709 |
rs370061810 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568545 | AGTTCTCAATGGTGA[A/G]TGAGGACCATTGATG | 6709 |
rs370062384 | snp | A/G | 8.33507e-05 | 0.00645511 | missense | SPTAN1 | GRCh38.p7 | 9:128583225 | ATGAAGTGGCAGCTC[A/G]TATGAATGAGGTGAT | 6709 |
rs370102482 | snp | C/T | 4.96989e-05 | 0.00498467 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128625969 | GGAGGCTCAGAGTCA[C/T]TTCCGCAAGGTGAGG | 6709 |
rs370108676 | snp | C/T | 1.64741e-05 | 0.00286998 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608099 | CTTGCTGAAGGGCCT[C/T]ATTTTCTCACCTGCC | 6709 |
rs370113838 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128626645 | CTGGTTTACCATGGA[A/G]GCCCTGGAGGAGACC | 6709 |
rs370135036 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629483 | AACCCTGGCTCGCCG[A/G]GTTTTAAAAGGGTAG | 6709 |
rs370219110 | snp | A/G | 0.000642795 | 0.017916 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617950 | AGAAGCACCAGAAGA[A/G]CTACCTGCTGTTAAC | 6709 |
rs370227601 | snp | A/G | 4.98401e-05 | 0.00499175 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615593 | AGCAGATAGCTGTGG[A/G]AGACCCAGTTTCTGA | 6709 |
rs370233387 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598530 | CCATCTTGGAGTGAG[G/T]CTCTGTTGCTGTAAG | 6709 |
rs370248959 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566087 | TTTCGGTTTTTGTTT[A/T]GTTTTGTCACCCAGG | 6709 |
rs370260978 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601235 | TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGTT | 6709 |
rs370304886 | snp | A/C/G | 0.000153988 | 0.00877328 | SPTAN1 | 9 | allele_origin=G(germline)/A(germline)/C(germline) | 9:128582740 | GAGCCATGCGTCGCC[A/C/G]GGCCCAGCTAGCCGA | 6709 |
rs370324040 | in-del | -/GAG | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586036 | TGAGAAGGAAGTTAG[-/GAG]AAGTAGTGATGCGCG | 6709 |
rs370351285 | snp | A/G/T | 0.000362348 | 0.0134555 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575162 | TTGTTAACAAATGTT[A/G/T]GTTGGTGACTCTGGC | 6709 |
rs370362654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614514 | AGAATTGCTTGAGCC[C/T]GGGAGGCAGAGGTTG | 6709 |
rs370404365 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590645 | TCATGTGGTCAGGAG[A/G]TTGAGACCATCCTGG | 6709 |
rs370415417 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631848 | AATCTTTGGCCACTG[C/T]TTCCTGGAGTCCTCG | 6709 |
rs370432744 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606500 | ATATTTTTTTTTTGG[G/T]GGGGGAAGCGTTTCG | 6709 |
rs370433340 | snp | A/C | 1.66685e-05 | 0.00288686 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632361 | AGGCTCAGCCCAGAG[A/C]AGGGGGAGGAAAAGA | 6709 |
rs370435310 | snp | C/T | 1.64901e-05 | 0.00287137 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128605169 | GGACCTTGCGGCTCT[C/T]GGTGACAAGGTGAGA | 6709 |
rs370439128 | snp | A/G | 1.64732e-05 | 0.0028699 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584699 | CATGGTTGGATAACT[A/G]GGGACTGGTGTCTGC | 6709 |
rs370450528 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597808 | GGCGCCTGCCACCGC[A/G]CCTAGCTAATTTTTG | 6709 |
rs370479127 | in-del | -/A | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597537 | AAAAAAGACAAAAAA[-/A]CTACAGTTAATGAAG | 6709 |
rs370483624 | in-del | -/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602396 | AATTTTTATATTTTT[-/T]AGTAGAGACGGGGTT | 6709 |
rs370501393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571572 | CTTGGGCAACAAGAG[C/T]GAAATTCTGTCTGAA | 6709 |
rs370508568 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569946 | ATTACTAATAATGAT[A/G]ATTGTAAATAGGAAA | 6709 |
rs370609436 | snp | C/T | 3.30284e-05 | 0.00406363 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128611740 | GAAGCACCAGGCTTT[C/T]GAAGCAGAGCTGCAT | 6709 |
rs370618630 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601608 | AAAAAAGTAGGCCTT[C/G]TCCTCATTAGTACAG | 6709 |
rs370624702 | snp | C/G | 1.65086e-05 | 0.00287298 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128626411 | GGACCTCTTCCTGAC[C/G]TTCGCCAAAAAGGCT | 6709 |
rs370640807 | snp | A/G | 9.89201e-05 | 0.00703209 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128609260 | AGCGAGTGATGAGTC[A/G]TACAAGGATCCCACC | 6709 |
rs370654629 | snp | A/G | 0.000132059 | 0.00812478 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632503 | AGTTCAGCCTTACTC[A/G]CCCTGGCTGGGTGGG | 6709 |
rs370695453 | snp | C/T | 1.66944e-05 | 0.0028891 | missense | SPTAN1 | GRCh38.p7 | 9:128577487 | GCAGAGAGACATGCA[C/T]GGCTCAATGATTCAT | 6709 |
rs370704701 | snp | C/T | 0.00021543 | 0.0103763 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605481 | TAGCGATTTCCGGTA[C/T]GGAGCCATGTTCACT | 6709 |
rs370705867 | snp | C/T | 0.000433825 | 0.0147216 | SPTAN1, WDR34 | 9 | allele_origin=T(germline)/C(germline) | 9:128633194 | AGGCACCAGGTGCCA[C/T]CTCTTACCCCACAGA | 6709 |
rs370711288 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595581 | AATTCACAAAGCTAG[C/G]CATTTTAAACTGTAC | 6709 |
rs370720243 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586183 | GACTGCAATGTTACA[A/G]TTGTGGCTCACTGCA | 6709 |
rs370734664 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605660 | ACCAGCCTGGGCTAC[A/G]TGGCGAAACCCTATT | 6709 |
rs370741251 | snp | C/T | 3.31131e-05 | 0.00406884 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615617 | TTTCTGACCCTCTTA[C/T]GTCCCCTGCCCCAGG | 6709 |
rs370748662 | snp | C/T | 3.29451e-05 | 0.00405851 | missense | SPTAN1 | GRCh38.p7 | 9:128591520 | GTCAGGGTTTTGTGC[C/T]GGCTGCGTACGTGAA | 6709 |
rs370750940 | snp | A/C | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554246 | GGAGGATTTTTGCTT[A/C]ATCCTGGACAAGTGT | 6709 |
rs370754689 | snp | C/G/T | 3.30274e-05 | 0.0040636 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605259 | CTGCAGAGCATACCC[C/G/T]CTTACTGCAAGCTCA | 6709 |
rs370762046 | in-del | -/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606508 | TTTTTGGGGGGGGAA[-/G]CGTTTCGCTTTTGTG | 6709 |
rs370762542 | snp | C/T | 6.60753e-05 | 0.00574746 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632401 | CTGCTGTGTGGAGGG[C/T]CTGTTCCCTAATTTC | 6709 |
rs370765693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601026 | TCTCGCTCTGTTGCC[C/T]AGGCTGGAGTGCAGT | 6709 |
rs370807034 | snp | C/T | 4.95029e-05 | 0.00497484 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128575297 | AGATATGGCTGCTCA[C/T]GAAGAAAGAGTTAAT | 6709 |
rs370818235 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128553103 | CCCGCACCGCCCCCG[A/G]TCCCTTCCCTCGGCC | 6709 |
rs370824213 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626338 | CACCTCCTGCACTGC[A/G]TCGGCACGTCCAGCC | 6709 |
rs370827330 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570707 | TGTTGCCCCGGCTGG[A/G]GTGGAATGGCACGAT | 6709 |
rs370856065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607418 | TTCCTCTGAGAAATT[C/T]GGACTTTTAAAAAAA | 6709 |
rs370866131 | in-del | -/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567463 | GCCCAGCTAATTTTT[-/T]GTATTTTTAGTAGAG | 6709 |
rs370884916 | snp | A/G | 4.94181e-05 | 0.00497057 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577294 | TTTTACAAGCAGCTG[A/G]TTCTGTAAATAAGTT | 6709 |
rs370897530 | snp | C/T | 6.84463e-05 | 0.00584965 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626029 | CAGCTCAAGGAAGGA[C/T]GCCCACCTTCTGTCT | 6709 |
rs370956360 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611875 | CTCCCGGTGCCCAGG[A/G]AGGAAGATGACCACC | 6709 |
rs370989926 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625723 | AGGAAGAGCAAGTTC[C/T]AGTCCTGTGGAGTCA | 6709 |
rs371017342 | snp | A/G | 4.95282e-05 | 0.00497611 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128566848 | ACTCTCAACCCTTAG[A/G]CGTCAGAAGCTGGAA | 6709 |
rs371055930 | snp | C/T | 3.29565e-05 | 0.00405921 | missense | SPTAN1 | GRCh38.p7 | 9:128615791 | CTGAATGAATCCCAT[C/T]GCCTGCACCAGTTCT | 6709 |
rs371083626 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600766 | CTCCCCAGTTCGAGC[A/G]ATTCTCCTGCCTCAG | 6709 |
rs371095095 | snp | A/G | 6.96901e-05 | 0.00590256 | missense | SPTAN1 | GRCh38.p7 | 9:128626610 | ATCAAGAGCTTCCGC[A/G]TAGCCTCCAACCCCT | 6709 |
rs371100708 | snp | C/T | 6.60829e-05 | 0.00574779 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128608906 | TCTGCAGGCCTTTGC[C/T]GACCAGCTCATCGCT | 6709 |
rs371105225 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609827 | CATTCAAGTGTCCCT[G/T]TGGGATGTGGCTTTT | 6709 |
rs371107458 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600961 | AGTCACAGCACACAG[C/T]CAGGGAGAAAGTCTT | 6709 |
rs371148094 | snp | A/G/T | 3.30509e-05 | 0.00406504 | missense | SPTAN1 | GRCh38.p7 | 9:128576887 | ATGCAGCCTGGCAGC[A/G/T]GCTGAAGGGCCTGGC | 6709 |
rs371177004 | snp | C/T | 1.65299e-05 | 0.00287483 | missense, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633318 | TGGAGTTCACCCGCT[C/T]GCTTTTCGTGAACTG | 6709 |
rs371178746 | snp | G/T | 4.94279e-05 | 0.00497107 | missense | SPTAN1 | GRCh38.p7 | 9:128582554 | GCCACTCGCCGAGAT[G/T]CTGTAAGTTTGTAGG | 6709 |
rs371182687 | snp | C/T | 1.64977e-05 | 0.00287203 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619016 | CAGGTGAGACAGAAA[C/T]CAAAGGTGTCACCTG | 6709 |
rs371221363 | snp | A/G | 3.30513e-05 | 0.00406504 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608293 | TGAGGCCTCTGGACC[A/G]TGGAGTTGGAGTCTG | 6709 |
rs371231421 | snp | A/C/G | 4.98114e-05 | 0.00499035 | missense | SPTAN1 | GRCh38.p7 | 9:128587697 | AAGCACAGTCCTGCC[A/C/G]GGTAAACTTGTAACA | 6709 |
rs371267756 | snp | C/T | 1.64917e-05 | 0.00287151 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630414 | CCAGCAGAGACCCTT[C/T]ACCCAGCCACCCCCC | 6709 |
rs371275512 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559695 | AAATAAATAAGTCTA[A/C]CCCTAATTGTTTACC | 6709 |
rs371292507 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606762 | AAGTGCTGGGATTAC[A/C]GGCGTGAGCCACTGC | 6709 |
rs371322683 | snp | C/T | 1.65351e-05 | 0.00287528 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584263 | AAGTAAAGTCTGCTC[C/T]GTCCTTTTGCATTCC | 6709 |
rs371347837 | in-del | -/CTTAA | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128553405 | GCTCAAATCAAATAA[-/CTTAA]TAGCTTAGCGTTCTT | 6709 |
rs371350283 | snp | C/T | 0.000283908 | 0.0119111 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566981 | ACCAACTTGCAGGTA[C/T]GTCTGATCTCCTGGG | 6709 |
rs371366167 | snp | A/C | 3.45238e-05 | 0.0041546 | downstream-variant-500B, intron-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128634001 | CAAAGAGAGACAGAT[A/C]CGTGGAGTAAGAGAA | 6709 |
rs371372049 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592951 | TAACCCCACTAATTC[A/G]TGCATGCTTTTGCTG | 6709 |
rs371512732 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612470 | ACTACAGGTCACTCA[C/T]ATCCATAGGGAAGGC | 6709 |
rs371515405 | snp | A/G | 0.000167229 | 0.00914256 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593074 | TCTTGCAGAGCACCA[A/G]TGTCCACTGCTACCC | 6709 |
rs371568849 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128555415 | GTATTTGACGAGCAT[A/G]CAGAAAACGGGTTGC | 6709 |
rs371600732 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592612 | CTGGGTCATAAATAT[A/G]AGAGGAAAAAGATCA | 6709 |
rs371641680 | snp | C/T | 3.29973e-05 | 0.00406172 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580910 | CCTGACCATGTCTCC[C/T]ATGCCCCCAAGCTGA | 6709 |
rs371647052 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627726 | GTTGTTAGAGATCCC[A/G]GATTGAGTGGGACCA | 6709 |
rs371671054 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571965 | AGGCTCAAGTGGTTC[A/T]CCCACCTCAGCCTCC | 6709 |
rs371673291 | snp | C/T | 9.39011e-05 | 0.0068514 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592970 | ATGCTTTTGCTGTGC[C/T]CCCTCTGTGCAGGAC | 6709 |
rs371679251 | snp | A/G | 6.60012e-05 | 0.00574423 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632551 | GCTGCCTGCTGAGCC[A/G]CCCTCGGCTTTGTGC | 6709 |
rs371679323 | snp | G/T | 0.000153988 | 0.00877328 | missense | SPTAN1 | GRCh38.p7 | 9:128612118 | CCCCAGGCCCGCCTG[G/T]CTGCCTTAGCTGACC | 6709 |
rs371687713 | snp | A/G | 1.66518e-05 | 0.00288542 | missense | SPTAN1 | GRCh38.p7 | 9:128621215 | GTCCACAAGGATCGC[A/G]TGAATGATGTCTGCA | 6709 |
rs371689420 | in-del | -/AGGGCTCTTC | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631146 | CACCACTCCCGGCCG[-/AGGGCTCTTC]ACTTTAAAGAAAGTC | 6709 |
rs371745652 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602212 | TTTTGTTTTTTTTGG[G/T]TTTTTTTTGTTTTTT | 6709 |
rs371751060 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562835 | CCGGGCGTGATGGCA[A/G]GCGCCTGTGGTCCCA | 6709 |
rs371770815 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567427 | CTCCCAGGTTGCTGG[A/G]ATTACAGGCGCCTGC | 6709 |
rs371776794 | snp | A/G | 1.64743e-05 | 0.00287 | missense | SPTAN1 | GRCh38.p7 | 9:128584831 | CAGAAGGGGAATGCC[A/G]TGGTGGAGGAAGGTG | 6709 |
rs371781354 | snp | A/G | 3.29592e-05 | 0.00405938 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568904 | ACCATACGGGTGAGT[A/G]TGAGTAGCTCGTGGA | 6709 |
rs371795692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616893 | GCCAAGATCGTGCCA[C/T]TGCACTCCATCCTAG | 6709 |
rs371871130 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589650 | GCATGATCTCAGCTC[A/C]CTACAAGCTCCACCT | 6709 |
rs371874064 | snp | A/C/G | 0.000495659 | 0.015735 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630234 | AATGTGAGGTTGCCA[A/C/G]GCATTGCTCTCTCTG | 6709 |
rs371912740 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610725 | AAAACCATATCAGGC[A/G]CCCAGGATCAGGAGC | 6709 |
rs371920094 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128633147 | CATCCTGAGACCTGG[A/G]AGGTCGGGTTTGAAG | 6709 |
rs371984764 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620585 | TAGCTGGGTGTGGTG[A/G]TGCACACCTGTAATC | 6709 |
rs371990099 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602785 | GGATTACAGGCTCAC[A/G]CCACCGTGCCCAGCT | 6709 |
rs371997163 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565763 | TTTCCAGGGTAACAC[A/G]ATTTTATACCTTTTA | 6709 |
rs372062686 | snp | A/G | 3.3065e-05 | 0.00406588 | missense | SPTAN1 | GRCh38.p7 | 9:128584375 | AAACAGGAAGCCCTC[A/G]TGGCTCGCTATGAGG | 6709 |
rs372100664 | snp | C/T | 6.59435e-05 | 0.00574172 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609007 | GCACTGACATAGTCA[C/T]CAGCCCTGAGAGGAT | 6709 |
rs372102532 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557265 | ATGTCTCTTACATCC[A/G]GTGCATTCAACTTGC | 6709 |
rs372157740 | snp | C/T | 6.58989e-05 | 0.00573978 | missense | SPTAN1 | GRCh38.p7 | 9:128578117 | TTCCCTAGGCTTCAA[C/T]GCTTCCTTGCTGACT | 6709 |
rs372185670 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560233 | GGATTACAGGCGCAC[A/G]CCGCCACACCTGGCT | 6709 |
rs372196146 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575685 | TGCTAAGTTAGTATT[A/G]GCAGATGTCCACCAA | 6709 |
rs372198447 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561329 | GTGAGTCAAGATCGC[A/G]CCACTGCAATCCAGC | 6709 |
rs372203791 | snp | G/T | 0.000397456 | 0.0140915 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582864 | AGTAATGTACTGTTA[G/T]TGTTGCCATGTAGCA | 6709 |
rs372206605 | snp | A/G | 1.65362e-05 | 0.00287538 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591644 | AGGATGACACTGGGG[A/G]CCGCAAGGGCTAGGC | 6709 |
rs372214130 | snp | A/C/G | 1.64841e-05 | 0.00287085 | missense | SPTAN1 | GRCh38.p7 | 9:128625910 | CTCATGAAGAGGTGG[A/C/G]GCCAGCTTCTGGCCA | 6709 |
rs372231764 | snp | C/T | 6.63229e-05 | 0.00575822 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582880 | TGTTGCCATGTAGCA[C/T]TCGATTAGTAAGCTA | 6709 |
rs372260439 | snp | G/T | 1.65386e-05 | 0.00287559 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578274 | TAGAATCTTCCAGAA[G/T]TGAAGATTTTAGCTT | 6709 |
rs372292829 | snp | A/G | 1.65138e-05 | 0.00287343 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617615 | GTGCAGAGACTGACT[A/G]TGCTGTTTCCCATCT | 6709 |
rs372294933 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567223 | CCTTGATACTACTGG[C/T]GAGCTTTAAACATTT | 6709 |
rs372307294 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593934 | CGGCCTGGGGATAAG[C/T]GTGCCTGGCTGTTCT | 6709 |
rs372367076 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623792 | ATTTCTTTAGAATTA[A/C]TTCCTTGGACCGGCT | 6709 |
rs372399781 | snp | A/C/T | 3.29795e-05 | 0.00406065 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611883 | GCCCAGGGAGGAAGA[A/C/T]GACCACCGTCACTGT | 6709 |
rs372522169 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609554 | CAAATGCTGAGCTTC[C/T]TGGGGGAAGTATGAC | 6709 |
rs372552458 | snp | G/T | 0.0926964 | 0.194308 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599482 | AGACAAAAAAAGTTG[G/T]TTTTTTTTTTTTTCG | 6709 |
rs372559841 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606040 | TAGTACATAATCAAT[A/G]TAAAATAGTCAAACT | 6709 |
rs372621227 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617549 | CAGAAAGATTAGTAG[A/G]TGTCTGTGAGGTCCA | 6709 |
rs372629136 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597947 | AGCCACCGCACCCGG[A/C]CTGTTTTGTTTTGTT | 6709 |
rs372649788 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595419 | CTGGCCTGTGTAGCT[A/G]TTTTTAAAAGACTTT | 6709 |
rs372663864 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561857 | GTTTCTTTATTTCCA[A/G]GCTCTGAATATAATT | 6709 |
rs372664308 | snp | C/T | 4.9788e-05 | 0.00498914 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626340 | CCTCCTGCACTGCGT[C/T]GGCACGTCCAGCCCT | 6709 |
rs372752614 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583465 | TTTGGTAAATGTGGT[C/T]GAGCATACTGGTTGG | 6709 |
rs372776563 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613335 | TTTCCAGAATGCTGA[A/G]TATACACCACACAGT | 6709 |
rs372779649 | snp | C/T | 0.000109828 | 0.00740958 | missense | SPTAN1 | GRCh38.p7 | 9:128632127 | TCCCCACCCCTGCAG[C/T]GCAAGCACCAGGAAA | 6709 |
rs372782253 | snp | C/T | 3.3173e-05 | 0.00407252 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128624375 | GATGAAGGGCCTGAA[C/T]GGGAAAGTGTCAGAC | 6709 |
rs372785209 | snp | A/G | 1.65195e-05 | 0.00287393 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128585788 | GGCCAAGCTTCACGA[A/G]CTGAACCAAAAGTGG | 6709 |
rs372798743 | snp | A/G | 1.66613e-05 | 0.00288623 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624292 | GTAACCACAGCAGGT[A/G]AGGCTGACCAGTGTG | 6709 |
rs372807389 | snp | A/T | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant | SPTAN1 | GRCh38.p7 | 9:128593013 | GGAGGCCGGCAGTGT[A/T]TCTCTGCGTATGAAG | 6709 |
rs372819699 | snp | A/G | 0.000115868 | 0.00761056 | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633361 | GGTCACCCACCCCTC[A/G]CTGCTTGCCCTGCGT | 6709 |
rs372824493 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563504 | TTTAGTCATTAGGTT[A/G]ACACCTAGTTGTGTA | 6709 |
rs372825476 | snp | C/T | 0.000201633 | 0.0100387 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128627463 | GGAGTTTGCCCAGCA[C/T]GCCAACGCCTTCCAC | 6709 |
rs372826052 | snp | A/G | 1.65767e-05 | 0.00287891 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588782 | GGACGTGTTTTTACC[A/G]TGTTTGCCCTTCCTT | 6709 |
rs372827106 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573362 | AAACCTCACTTGAGA[G/T]GTACCACAAACTGTC | 6709 |
rs372831978 | snp | C/G/T | 0.000105935 | 0.00727725 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128604364 | CCTACAGCAGCTGGC[C/G/T]GAGGAACGGAGCCAG | 6709 |
rs372851633 | snp | A/G | 0.00102642 | 0.0226308 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604447 | CTGGGCTGGGAGAGG[A/G]AGAAACAGGTGACTG | 6709 |
rs372860106 | snp | A/G | 0.000280156 | 0.0118321 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582677 | CTAGAGACTCACAGG[A/G]GATCCTTGTCTTTCA | 6709 |
rs372877240 | snp | C/G | 4.97929e-05 | 0.00498939 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581928 | TGCTTTCAAATGACC[C/G]TTATAGTAAGCCAGA | 6709 |
rs372887620 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604279 | GTCTGACTGGGGGCA[C/T]GACAGGAGAGGGAGT | 6709 |
rs372896131 | snp | A/G | 0.000167853 | 0.0091596 | SPTAN1 | 9 | allele_origin=G(germline)/A(germline) | 9:128585983 | AACCAGGCGTGGGAA[A/G]CGTCTCACCTGCCAG | 6709 |
rs372907681 | snp | C/T | 0.000214124 | 0.0103449 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575185 | ACTCTGGCTCTCTTA[C/T]GGTCCCTGAATAGGA | 6709 |
rs372920597 | in-del | -/TATTTTTTTTT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570329 | ATATATATATATATA[-/TATTTTTTTTT]TTTTTTTTTTTTTTT | 6709 |
rs372937374 | snp | C/T | 0.000132033 | 0.00812398 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580876 | TCTGCCTCGGAGGCA[C/T]TGGGGCTGACCTCAT | 6709 |
rs372969086 | snp | C/T | 3.29875e-05 | 0.00406112 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594157 | TGTCCCTCTTGTCAC[C/T]CTCTTGAATTCCATC | 6709 |
rs373006510 | snp | A/G/T | 0.000131776 | 0.00811621 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603508 | AATTGCCAGACACTT[A/G/T]ATTAGTTTTGCCTTC | 6709 |
rs373012192 | snp | C/G | 1.64993e-05 | 0.00287218 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580908 | TCCCTGACCATGTCT[C/G]CTATGCCCCCAAGCT | 6709 |
rs373016934 | snp | C/T | 1.654e-05 | 0.00287571 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587587 | CTGCACAGTGCTCCA[C/T]GTGTGGTTTTGGTTT | 6709 |
rs373018123 | snp | A/C | 4.99563e-05 | 0.00499756 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583044 | GACGTTCTCAGGTTC[A/C]AGATAGAAAGAACCC | 6709 |
rs373021914 | in-del | -/GGG | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602210 | TTTTTTGTTTTTTTT[-/GGG]TTTTTTTTGTTTTTT | 6709 |
rs373022604 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619204 | AACAAAATTGGTATG[A/G]CTTTGTCAGTCTCAG | 6709 |
rs373030015 | snp | A/G | 1.6483e-05 | 0.00287076 | missense | SPTAN1 | GRCh38.p7 | 9:128582784 | CAGCAGTTTTTCCGT[A/G]ATTCTGATGAGCTCA | 6709 |
rs373031760 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588994 | GCTGGCACCTCCACG[C/T]ATGCTCAGTTGGGTT | 6709 |
rs373033857 | snp | C/T | 9.88468e-05 | 0.00702948 | missense | SPTAN1 | GRCh38.p7 | 9:128608014 | AAGGCCTGGGTTCAG[C/T]GCAGGATGATGCTGG | 6709 |
rs373069514 | snp | A/G | | | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128550737 | GGGAGCTACAATTGT[A/G]TTAGCCATTTTGTAC | 6709 |
rs373072698 | snp | C/G | 0.000195981 | 0.00989706 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609618 | GTCCACATCAGTGTA[C/G]TGAACTCTTGTTCTT | 6709 |
rs373224130 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613811 | GAGTTCGAGACCACT[C/T]CGGCCAACGTGGTGA | 6709 |
rs373259652 | snp | A/G/T | 1.64985e-05 | 0.0028721 | missense | SPTAN1 | GRCh38.p7 | 9:128626515 | AAATCAAAGCTTTGC[A/G/T]CGAGGCCCACGACGC | 6709 |
rs373286978 | snp | A/G | 1.64754e-05 | 0.00287009 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609104 | CTCATGTTGGATCTC[A/G]TGGTTTCACTCTTTC | 6709 |
rs373307608 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558437 | CTTAGCACTTCATTT[C/T]CCCTCCTTCAGTCTC | 6709 |
rs373315870 | snp | C/T | 1.67399e-05 | 0.00289304 | downstream-variant-500B, synonymous-codon | SPTAN1, WDR34 | GRCh38.p7 | 9:128633819 | CGTGAACTCTGTGCT[C/T]AGCTGCCACACCTTC | 6709 |
rs373344051 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589526 | CGTGATCCACCCACC[C/T]CAGCCTCCCAAAGTG | 6709 |
rs373387372 | snp | G/T | 0.000131796 | 0.00811668 | SPTAN1 | 9 | allele_origin=G(germline)/T(germline) | 9:128598944 | TAATAATAAAACTGG[G/T]TTCTCTCTCTCCTTG | 6709 |
rs373416195 | snp | C/T | 6.62943e-05 | 0.00575698 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626361 | GTCCAGCCCTGGCGA[C/T]TCCGCCAACTCAGTC | 6709 |
rs373418441 | snp | C/T | 8.37626e-05 | 0.00647104 | downstream-variant-500B, missense | SPTAN1, WDR34 | GRCh38.p7 | 9:128633790 | AGGTCCTCAGCTTCC[C/T]GGGGCCCTTGTTCCG | 6709 |
rs373426828 | snp | C/T | 1.65985e-05 | 0.00288079 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128624408 | GGAGAAAGCTGCAGC[C/T]CAGAGAAAGGCGAAG | 6709 |
rs373441301 | snp | G/T | 1.64947e-05 | 0.00287177 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605195 | TGAGAGGACCCAAAG[G/T]CATCTTCTGTCTGGC | 6709 |
rs373455470 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612797 | CAGGCGTGGTGGCAC[A/G]CTCCTGTAATCCCAG | 6709 |
rs373460078 | snp | A/G | 0.000361393 | 0.0134375 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588979 | GTGTGTTTGTTCCAC[A/G]CTGGCACCTCCACGT | 6709 |
rs373491498 | snp | A/G | 0.000214272 | 0.0103484 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128613443 | TGTGAACAACCTGCT[A/G]AAAAAGCATCAACTG | 6709 |
rs373503519 | snp | C/G | 1.65094e-05 | 0.00287305 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574647 | AGCCAGTTGTGATCT[C/G]ATTAAAACTCTGATT | 6709 |
rs373506212 | snp | A/G | 9.98668e-05 | 0.00706565 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617789 | CTTCTGGCCAAGAGG[A/G]CAGAGGTGTTTGAGT | 6709 |
rs373542926 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582672 | GAACACTAGAGACTC[A/G]CAGGGGATCCTTGTC | 6709 |
rs373543501 | snp | A/G/T | 8.63336e-05 | 0.00656968 | downstream-variant-500B, intron-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128634003 | AAGAGAGACAGATAC[A/G/T]TGGAGTAAGAGAAAC | 6709 |
rs373558927 | snp | A/C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603886 | GCAGTGAGCGGCTTC[A/C/T]TTGCCGCCTGCAGTG | 6709 |
rs373596450 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626122 | GTGTGGCTGGCATCA[A/G]TTAAAACCAGGGCAA | 6709 |
rs373650761 | snp | A/C/G | 3.29464e-05 | 0.00405861 | synonymous-codon, missense | SPTAN1 | GRCh38.p7 | 9:128609156 | CAGATGATTGAGAAA[A/C/G]GGTCAAAGCTAGGAG | 6709 |
rs373652697 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572238 | CTGCTTCTCTGAAGG[C/T]TCCTGTTGCTTGCTT | 6709 |
rs373682033 | in-del | -/AT | 0.00636936 | 0.0560724 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614969 | TCTATATGTTGACAC[-/AT]GTGATTATATGATAT | 6709 |
rs373714851 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581489 | CAAAAAAAAAAAAAA[A/C]AAACAAAAAAAACAA | 6709 |
rs373772795 | snp | A/G | 1.68496e-05 | 0.0029025 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632962 | CTCTACCAGGTATGG[A/G]CCTCAGGAGGTGGGT | 6709 |
rs373795702 | in-del | CC/GAA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623178 | CTCCCACCTGAGCTT[CC/GAA]CTAGCTAGCTGGGAC | 6709 |
rs373857333 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128608222 | AGACTCACTGGACAG[C/T]GTAGAGGCTCTGATC | 6709 |
rs373933792 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590374 | TAAGCCCTTAAAATA[C/T]GGCTAGTACAACTGG | 6709 |
rs373935353 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625413 | CACTGCAGGAGCACT[C/T]ACTCAGTTTTCAGCA | 6709 |
rs373940620 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594867 | GAGTCTCTCTTTTGT[C/T]GCCCAGGCTGGAGTG | 6709 |
rs373952081 | snp | C/T | | | downstream-variant-500B, missense | SPTAN1, WDR34 | GRCh38.p7 | 9:128633812 | CTTGTTCCGTGAACT[C/T]TGTGCTCAGCTGCCA | 6709 |
rs373973880 | snp | G/T | 0.000164742 | 0.00907435 | missense | SPTAN1 | GRCh38.p7 | 9:128582732 | TCACGAGAGAGCCAT[G/T]CGTCGCCGGGCCCAG | 6709 |
rs373986338 | snp | C/T | 1.79277e-05 | 0.00299392 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609331 | TGTAGCCTTATGTTA[C/T]TGAGTAGATTTTGTT | 6709 |
rs373988544 | snp | C/T | 4.94336e-05 | 0.00497135 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128605118 | TGATCTCGCCAGTGT[C/T]CAGGCCCTGCAACGC | 6709 |
rs373990901 | snp | A/G | 6.69232e-05 | 0.00578421 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632330 | CCAGGCCAGGTACCC[A/G]GGAGGGCTGTGGGCC | 6709 |
rs374053890 | in-del | -/AAAATACAAA | 0.0150606 | 0.0854603 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590688 | AACCCCGTCTCTACT[-/AAAATACAAA]AAAATTAGCTGTGCG | 6709 |
rs374077887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595492 | TGCTATGTTCTCTAC[A/G]TGTTGTTATAAGAAC | 6709 |
rs374088892 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620067 | TCAGACAGGCAAAGG[A/C]AGGAGCTGCAAGATG | 6709 |
rs374094161 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600972 | ACAGCCAGGGAGAAA[A/G]TCTTTTTTTTTTTTT | 6709 |
rs374104296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581992 | GATGAAAGATTCATA[C/T]GCAGAGTACTCCTGT | 6709 |
rs374110210 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578790 | GCCAAGATCACACCA[G/T]TCCACTCCCGTCCGG | 6709 |
rs374110359 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563628 | ATTCGTTATGGAGCT[C/T]TCTCCCTACCCCTTA | 6709 |
rs374129834 | in-del | -/AG | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128555498 | GAATGATCCAAAGAA[-/AG]GGGGAAAAAAACCCT | 6709 |
rs374135919 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558082 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 6709 |
rs374186379 | snp | A/G | 9.89348e-05 | 0.00703261 | missense | SPTAN1 | GRCh38.p7 | 9:128591615 | CTGCGGCAGGAGCAG[A/G]TTGACAATCAGTAAG | 6709 |
rs374241065 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560741 | AGAGGGAGTGAAGGC[A/C]GGGTGCTGTGGCTCA | 6709 |
rs374248187 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577959 | TTGCTTTCCTTCACA[A/G]TCTAGATTGGGAAAT | 6709 |
rs374248373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560129 | CGCTCTGTCGCCCAG[A/G]CTGGAGTGCAAAGGC | 6709 |
rs374295471 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566405 | TATTTGAATACCACA[G/T]TTGCTGTTTCCTCTG | 6709 |
rs374320973 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615191 | CCGAGTATCTGTGAG[A/G]TACCAAGTCTGAATG | 6709 |
rs374391741 | snp | A/G | 0.000307953 | 0.0124049 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608826 | TGGCAGTCCAGGCAG[A/G]GCCCAGCCACAGGCC | 6709 |
rs374394049 | snp | A/G | 3.29451e-05 | 0.00405851 | missense | SPTAN1 | GRCh38.p7 | 9:128608140 | TTTAGCTGTTCCATC[A/G]GGACTGTGAGCAAGC | 6709 |
rs374405583 | snp | C/T | 9.9295e-05 | 0.0070454 | synonymous-codon, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633238 | ACAAGCCGACTACTG[C/T]GTCTCCCACATGAAG | 6709 |
rs374443036 | snp | G/T | 1.67809e-05 | 0.00289658 | missense | SPTAN1 | GRCh38.p7 | 9:128583253 | GATCAGTTTGTGGAA[G/T]AAACTGCTAGAGGCC | 6709 |
rs374470645 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557848 | TCGCTCTGTCGCCCA[C/G]GCTGGAGTGCAGTGG | 6709 |
rs374478564 | snp | A/G | 4.94776e-05 | 0.00497357 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128580948 | TTCCGAGGAGAGAGC[A/G]GCGCTGCTGGAGCTG | 6709 |
rs374482693 | snp | C/T | 2.93483e-05 | 0.00383057 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626698 | TCAAGGTACACCTCC[C/T]GCTGCCCTCAGGAGC | 6709 |
rs374485499 | snp | A/G | 1.64836e-05 | 0.0028708 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576963 | CTTTAACAGGTGTCA[A/G]GCCAGAGTGGGCTTT | 6709 |
rs374489181 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578081 | GAACCTCCGCTGGAA[A/G]CATAATGTCTTCCTT | 6709 |
rs374500733 | snp | A/T | 0.000153988 | 0.00877328 | missense | SPTAN1 | GRCh38.p7 | 9:128608917 | TTGCCGACCAGCTCA[A/T]CGCTGCCGGCCATTA | 6709 |
rs374506067 | snp | A/G | 1.64765e-05 | 0.00287019 | missense | SPTAN1 | GRCh38.p7 | 9:128583947 | AACATGCACTGCTAG[A/G]GGCAGATGTGGCTGC | 6709 |
rs374511397 | snp | C/T | 1.64784e-05 | 0.00287035 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128625876 | TCAGTCCAAGGCCAT[C/T]GAGGCCCGGCACGCC | 6709 |
rs374524469 | snp | C/T | 0.000153988 | 0.00877328 | missense | SPTAN1 | GRCh38.p7 | 9:128580947 | TTTCCGAGGAGAGAG[C/T]GGCGCTGCTGGAGCT | 6709 |
rs374574349 | snp | C/G/T | 0.000382145 | 0.0138178 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594407 | CTCAGCTGAAAATTT[C/G/T]TTTAAAGATTTGAGT | 6709 |
rs374578900 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128566858 | CTTAGGCGTCAGAAG[C/T]TGGAAGATTCCTATC | 6709 |
rs374583857 | snp | A/C | 3.29544e-05 | 0.00405908 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578063 | AGGCCATTTTCCACC[A/C]TGGAACCTCCGCTGG | 6709 |
rs374586176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616749 | TCCAGAGCAAGACTC[C/T]GTCTCAAAAAAATAA | 6709 |
rs374625039 | snp | A/G | 1.64787e-05 | 0.00287038 | missense | SPTAN1 | GRCh38.p7 | 9:128615792 | TGAATGAATCCCATC[A/G]CCTGCACCAGTTCTT | 6709 |
rs374654113 | snp | A/C | 0.000437904 | 0.0147905 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593107 | TCCATTCTCCCTCTG[A/C]CGCTTCTCTTGAAGG | 6709 |
rs374682395 | snp | G/T | 4.94189e-05 | 0.00497062 | missense | SPTAN1 | GRCh38.p7 | 9:128591569 | GTCAGCCTCCCGGGA[G/T]AATCTCCTGGAGGAG | 6709 |
rs374718055 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630423 | ACCCTTCACCCAGCC[A/G]CCCCCCAGGGTACCC | 6709 |
rs374723711 | snp | A/C/T | 4.94184e-05 | 0.00497063 | missense | SPTAN1 | GRCh38.p7 | 9:128612161 | TGGTGCAAAAGTCAG[A/C/T]GGAAAAGAGCCAGAA | 6709 |
rs374756919 | snp | A/G/T | 0.000127528 | 0.00798437 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592968 | GCATGCTTTTGCTGT[A/G/T]CCCCCTCTGTGCAGG | 6709 |
rs374760508 | snp | C/G | 4.94173e-05 | 0.00497053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627952 | CGATGGGTTAATATT[C/G]TTTTCTTCCTTCTCT | 6709 |
rs374801331 | snp | A/G | 4.94915e-05 | 0.00497426 | missense | SPTAN1 | GRCh38.p7 | 9:128608940 | GGCCATTATGCCAAG[A/G]GAGACATTTCTAGCC | 6709 |
rs374805926 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593108 | CCATTCTCCCTCTGC[C/T]GCTTCTCTTGAAGGC | 6709 |
rs374831136 | snp | A/C/G/T | 4.97504e-05 | 0.00498732 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591659 | GCCGCAAGGGCTAGG[A/C/G/T]GTCCCATAGGCATAC | 6709 |
rs374834326 | snp | C/G | 4.9458e-05 | 0.00497258 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607839 | TACCTAATCCCTTCC[C/G]TCCTTTTGGCAGGAA | 6709 |
rs374838123 | snp | A/G | 0.000281641 | 0.0118634 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582872 | ACTGTTAGTGTTGCC[A/G]TGTAGCACTCGATTA | 6709 |
rs374856374 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589741 | CCACCACGCCCGGCT[A/G]ATTTTTTGTATTTTT | 6709 |
rs374877320 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630928 | CAGGCAGGCTGGTCT[C/T]GAACTCCTGACCTCG | 6709 |
rs374893683 | snp | C/T | 3.29979e-05 | 0.00406175 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632648 | TCCCTGGGCTATGAC[C/T]TGCCCATGGTGGAGG | 6709 |
rs374954536 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564191 | TTTGGGAGGCCAAGG[C/T]GGGTGGATCACGAGG | 6709 |
rs374968240 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601098 | AAGCGATCCTCCTTC[C/T]TCAGCTCCCCTAGTA | 6709 |
rs374977921 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625194 | GGTCTGCCCTGGCCC[C/T]TTCACTGGTTGAAAT | 6709 |
rs375003647 | snp | A/G/T | 0.000176294 | 0.00938711 | downstream-variant-500B, utr-variant-3-prime | SPTAN1, WDR34 | GRCh38.p7 | 9:128633715 | AAGGCTCGGCACAGC[A/G/T]AAGGCTTGCACCCGC | 6709 |
rs375016371 | snp | A/G | | | missense, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633315 | ACGTGGAGTTCACCC[A/G]CTCGCTTTTCGTGAA | 6709 |
rs375026050 | snp | C/G/T | 3.30306e-05 | 0.00406377 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128608915 | CTTTGCCGACCAGCT[C/G/T]ATCGCTGCCGGCCAT | 6709 |
rs375037363 | snp | C/G | 1.66651e-05 | 0.00288657 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585973 | CTGCTGAGGTAACCA[C/G]GCGTGGGAAGCGTCT | 6709 |
rs375051910 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128556692 | CAAGTTGAAATGAAT[C/T]AATCAGTTTGAAGGC | 6709 |
rs375056054 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596276 | TGTTCGTTTTTTTTG[-/T]TTTGTTTGTTTGTTT | 6709 |
rs375104532 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616154 | GGAGTTGCTTTTTTT[C/T]TTATTCTCTATCTGT | 6709 |
rs375107644 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560369 | GATTACAGGTGTAAG[A/C]CACCGTGCCCGCCTT | 6709 |
rs375111710 | snp | A/G | 6.59489e-05 | 0.00574196 | missense | SPTAN1 | GRCh38.p7 | 9:128585835 | AAGCTTCCCAGCGTC[A/G]GCAGGACCTGGAGGA | 6709 |
rs375134079 | in-del | -/AGGC | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631679 | AAAAATACAAAAATT[-/AGGC]AGGTGTGGTGATGGG | 6709 |
rs375135650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568230 | GAAGAACACTGCTTT[A/G]GGTACAATCCCTGCC | 6709 |
rs375171402 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561087 | CAATAAATAATATGT[C/T]GGCCAGGCACGGTGG | 6709 |
rs375172350 | snp | C/T | 9.95091e-05 | 0.00705299 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582882 | TTGCCATGTAGCACT[C/T]GATTAGTAAGCTAAA | 6709 |
rs375175883 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593977 | GTGAACAGTACAGTG[C/T]GCGCATATCTCTCAG | 6709 |
rs375181223 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584866 | ATTGGTATCAGTGAC[A/G]TGGCTTGGTGCTGCT | 6709 |
rs375195855 | snp | G/T | 6.60066e-05 | 0.00574447 | missense | SPTAN1 | GRCh38.p7 | 9:128615654 | TGAAGGACCTGAACA[G/T]CCAGGCAGACAGCCT | 6709 |
rs375199636 | snp | A/G | 6.58903e-05 | 0.00573941 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128612153 | GCAGTTCTTGGTGCA[A/G]AAGTCAGCGGAAAAG | 6709 |
rs375222598 | snp | C/T | 3.30251e-05 | 0.00406343 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605290 | TTCACCACTTTCTTC[C/T]CATAGGTAAACTCCC | 6709 |
rs375244012 | snp | C/T | 1.66849e-05 | 0.00288828 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613360 | CACAGTAGCCTTTGC[C/T]TTTTGTGTTTTCATT | 6709 |
rs375244907 | snp | A/G/T | 8.41696e-05 | 0.00648683 | missense | SPTAN1 | GRCh38.p7 | 9:128632190 | GAGGACCTGGGGGCC[A/G/T]CCATGGAGGAGGCCC | 6709 |
rs375294332 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128553105 | CGCACCGCCCCCGGT[C/G]CCTTCCCTCGGCCGG | 6709 |
rs375340239 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631896 | GTGCACTGCCCTCTG[A/G]CAGGTCTACCAGCTG | 6709 |
rs375343189 | snp | A/C | 0.000153988 | 0.00877328 | missense | SPTAN1 | GRCh38.p7 | 9:128581840 | TGGAAGCGCTTCTTA[A/C]GAAGCACGAAGACTT | 6709 |
rs375345721 | in-del | -/TA | 0.0119091 | 0.0762411 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580313 | TAAAAATAAAATATG[-/TA]TATATATATACATAT | 6709 |
rs375352590 | in-del | -/TTTG | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599501 | TTTTTTTTTCGGTCT[-/TTTG]TTTGTTTGTTTGTTT | 6709 |
rs375359818 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590204 | GAGGAAACCTGTGAT[C/T]CTTATCTTTCTATTG | 6709 |
rs375407120 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610036 | ACTTGCTATGAGCTC[A/G]TGGTGTTCGGTGGCC | 6709 |
rs375441905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630638 | AGGTCAAGCAATTCT[C/T]CTGCCTCAGCCTCCC | 6709 |
rs375481019 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562417 | AGATCTGTATGATAT[C/T]AGATGGTAGGGTTGG | 6709 |
rs375528151 | snp | C/T | 1.64868e-05 | 0.00287109 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617952 | AAGCACCAGAAGAGC[C/T]ACCTGCTGTTAACCT | 6709 |
rs375529649 | snp | A/C | 0.000149871 | 0.00865524 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605501 | CCATGTTCACTCAGA[A/C]TTCTGGAACATAGAG | 6709 |
rs375529819 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595221 | CTCAAGTGATTCTCA[G/T]GCCTCAGCCACCCGA | 6709 |
rs375540423 | in-del | -/C | 0 | 0 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128555622 | AATTTGCAAAGCCTT[-/C]TTTTTTTTTTTTTTT | 6709 |
rs375602967 | snp | C/T | 8.41163e-05 | 0.00648468 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567012 | ATTCCTGCCAAAATT[C/T]AAGAGCCCAAATGTT | 6709 |
rs375619488 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600726 | GGAGTGCAGTGGCAC[A/G]ATCTCGGCTCACTGC | 6709 |
rs375620332 | in-del | -/AG | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618121 | CCGGTGAGTAGTCAG[-/AG]GCAGGAGCTCCCGGG | 6709 |
rs375623472 | snp | C/T | 6.60458e-05 | 0.00574618 | missense | SPTAN1 | GRCh38.p7 | 9:128588825 | AACAAGTGGCCCCCA[C/T]GGATGATGAGACTGG | 6709 |
rs375636579 | snp | A/T | 4.94597e-05 | 0.00497266 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609014 | CATAGTCACCAGCCC[A/T]GAGAGGATGCATCCC | 6709 |
rs375648005 | snp | C/G | 0.00205793 | 0.0320114 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628022 | GGCCTGGCTTGTGGA[C/G]GATCCCGGGATGGGC | 6709 |
rs375649697 | snp | A/G | 9.91736e-05 | 0.00704109 | synonymous-codon, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633319 | GGAGTTCACCCGCTC[A/G]CTTTTCGTGAACTGA | 6709 |
rs375663540 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610614 | TGCATTTCTTACCCA[C/G]CCAATTGTTTTTCCC | 6709 |
rs375665107 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596185 | TTGTAGCACATACCA[C/G]TACTCCATTCCTTTT | 6709 |
rs375667545 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565859 | CTCAAAAACCTCTCT[A/G]TAGGCTGTAATTTTG | 6709 |
rs375682115 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572811 | CCGCCACCCACATCG[A/G]GTCCCACATCCGAGT | 6709 |
rs375684704 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591259 | TTTTAGTAGAGACGG[A/G]GTTTCACTGTGTTGG | 6709 |
rs375698853 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624728 | GTAAACGCTGCTGCA[C/T]GCAGAGATGGCATAA | 6709 |
rs375701844 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603643 | TTTTCTCCACTATCT[A/T]CCTTCCCTGTCTACA | 6709 |
rs375749920 | snp | C/T | 1.75471e-05 | 0.00296197 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604310 | GCAGTGGAGCTGATG[C/T]TTTGCTGTCCTGCAG | 6709 |
rs375765139 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609830 | TCAAGTGTCCCTGTG[A/G]GATGTGGCTTTTTCT | 6709 |
rs375771110 | snp | C/T | 6.58913e-05 | 0.00573945 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627978 | TCTCTGGGCTTGTCA[C/T]GTGGGGGTCTCGTGC | 6709 |
rs375772117 | snp | A/G | 0.000115311 | 0.00759224 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630315 | TCACTGTCCTTCCAC[A/G]TTTAGGTCCTGTATG | 6709 |
rs375843859 | snp | C/T | | | downstream-variant-500B, missense | SPTAN1, WDR34 | GRCh38.p7 | 9:128633902 | ACTCCAGACAGTAGA[C/T]AGGGCTTTCATCCTG | 6709 |
rs375865924 | snp | A/C | 6.60295e-05 | 0.00574547 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580887 | GGCATTGGGGCTGAC[A/C]TCATCTCCCTGACCA | 6709 |
rs375905397 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593155 | AGATGAGGTGGTGGG[A/G]GGAACTGCCTGTCCG | 6709 |
rs375941925 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617308 | CAGACATATATTGAT[A/T]TATTAATACATATTT | 6709 |
rs375943639 | snp | C/T | 1.6588e-05 | 0.00287988 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626345 | TGCACTGCGTCGGCA[C/T]GTCCAGCCCTGGCGA | 6709 |
rs375983687 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578512 | AAGTGCTACTACTTG[G/T]CACATTGATCCTTTG | 6709 |
rs376019489 | snp | A/G | 4.94425e-05 | 0.0049718 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568915 | GAGTATGAGTAGCTC[A/G]TGGAGTGGATGGCTT | 6709 |
rs376022494 | snp | C/T | 0.00016214 | 0.00900244 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128555331 | CTTGTTATCTTGCTC[C/T]TCCCCCTCCCTCTTT | 6709 |
rs376127976 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594429 | GATTTGAGTCTCTTG[A/T]TTTTTTTTTTTTTTT | 6709 |
rs376147583 | snp | C/G/T | 4.94828e-05 | 0.00497387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594158 | GTCCCTCTTGTCACC[C/G/T]TCTTGAATTCCATCA | 6709 |
rs376149683 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601086 | CTTCCCAGATTCAAG[C/T]GATCCTCCTTCCTCA | 6709 |
rs376164380 | snp | A/G | 5.1656e-05 | 0.00508186 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624510 | CTGTCAGCAAGGCCC[A/G]GAAGAGCCTTCCCAG | 6709 |
rs376196799 | snp | A/C/G | 0.00064442 | 0.0179386 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632757 | TGTGAGCCTCTGCCC[A/C/G]GGGCACCCACCTGCC | 6709 |
rs376208532 | snp | C/T | 1.65729e-05 | 0.00287857 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128626564 | CTCTGCCCAGGCTGA[C/T]TTCAACCAGCTGGCC | 6709 |
rs376228888 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564238 | AGCCTGGCCAACATG[A/G]TGAAACCCCGTCTCT | 6709 |
rs376238795 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600859 | GTAGAGACAGGGTTT[C/T]GCCATGTTGGCCAGG | 6709 |
rs376240538 | snp | G/T | 1.70188e-05 | 0.00291704 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626027 | CACAGCTCAAGGAAG[G/T]ACGCCCACCTTCTGT | 6709 |
rs376241751 | snp | C/T | 0.000145672 | 0.00853315 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592942 | CCTGTGGATTAACCC[C/T]ACTAATTCGTGCATG | 6709 |
rs376246064 | snp | A/G | 6.58924e-05 | 0.0057395 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627994 | GTGGGGGTCTCGTGC[A/G]CTTGCCCCTCGTGGC | 6709 |
rs376255893 | snp | C/G | 1.64776e-05 | 0.00287028 | missense | SPTAN1 | GRCh38.p7 | 9:128609240 | ATCAGTGAAAAATTG[C/G]AAACAGCGAGTGATG | 6709 |
rs376278535 | snp | C/T | 6.63647e-05 | 0.00576003 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588764 | ACTTAGATGACTCAG[C/T]GCGGACGTGTTTTTA | 6709 |
rs376280897 | snp | A/G | 4.95413e-05 | 0.00497677 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128577432 | TCAAGTGAAGCGAGA[A/G]GAACTGATTACAAAC | 6709 |
rs376308583 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613927 | GGAGAATCACTTGAG[C/T]CCAGGAGGCGGAGGT | 6709 |
rs376322897 | in-del | -/AAAAAT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601569 | TCTACAAATAAAAAT[-/AAAAAT]GTTTTAAAAAGAAGA | 6709 |
rs376334112 | snp | C/G | 5.01329e-05 | 0.00500639 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598369 | TGGCTTGCTATTTTG[C/G]GTTTTAGTTATTATG | 6709 |
rs376357226 | snp | C/T | 1.64814e-05 | 0.00287061 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625091 | GTATATTTTCCACAC[C/T]TCGTTTTCTAGGTGA | 6709 |
rs376385475 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614672 | AGTTACTTGGAGGCC[A/G]AGGCGGGAGGTTCAC | 6709 |
rs376433063 | in-del | -/TT/TTT/TTTT | 0.111224 | 0.207945 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560084 | CACATCCACCTCACC[-/TT/TTT/TTTT]TTTTTTTTTTTTTTT | 6709 |
rs376436027 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626006 | CCACGTGAAGCTTAG[C/G]TGGCCCACAGCTCAA | 6709 |
rs376453109 | snp | A/G | 8.23716e-05 | 0.00641709 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608079 | GGTTTCTGACCAAGT[A/G]TTTCCTTGCTGAAGG | 6709 |
rs376482975 | snp | A/G | 1.64735e-05 | 0.00286993 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598998 | CAGGGTAAGTTTCGG[A/G]TGCTGTGTGTGGATC | 6709 |
rs376500539 | snp | A/G | | | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632231 | CAACAAGTACACGGA[A/G]CACAGCACCGTGGGC | 6709 |
rs376500906 | snp | A/G | | | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128552332 | CCTTGCGCGCGCCCC[A/G]TTTCCCCATCCTCCC | 6709 |
rs376519190 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561889 | GATCTATAATATGTG[C/T]CAAGTCCTGAGTTCT | 6709 |
rs376531572 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560872 | AGTACAAAAATTAGT[C/T]GCGTGTGGTGGCGGG | 6709 |
rs376544506 | snp | C/T | 0.00118064 | 0.0242678 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627195 | GCCTCTTCCTTGAAG[C/T]CCCTGGGGGGTGGGA | 6709 |
rs376560470 | snp | C/T | 2.05874e-05 | 0.00320831 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621305 | CCACTGGGACACCCA[C/T]GTGTTGGTACCACAG | 6709 |
rs376572315 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633351 | CCACTCCCTGGGTCA[C/T]CCACCCCTCGCTGCT | 6709 |
rs376626869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583721 | ACTAAGATACTACTG[C/T]TCATGGGCAGTGTTG | 6709 |
rs376637069 | in-del | -/TTT | 0 | 0 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560099 | TTTTTTTTTTTTTTT[-/TTT]AAGAGACAGAGTCTC | 6709 |
rs376726449 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625205 | GCCCCTTCACTGGTT[A/G]AAATGTATGCAGATA | 6709 |
rs376751145 | snp | A/C | 0.000181565 | 0.00952624 | SPTAN1 | 9 | allele_origin=A(germline)/C(germline) | 9:128581073 | AGGTAATCTGTGAGC[A/C]AAGCCTTGCCAGTGG | 6709 |
rs376756489 | snp | A/C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607380 | GGAGGGTGAAAAGAT[A/C/G]TTAATTATAAGCCTA | 6709 |
rs376768655 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567618 | GAGGAAGGCATAATA[A/G]TGATGTTGCTGGCAA | 6709 |
rs376812195 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602144 | AATGTCACCTAGGGA[C/T]GCCATGAGGACATCT | 6709 |
rs376859845 | snp | A/G/T | 3.33379e-05 | 0.00408265 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632360 | CAGGCTCAGCCCAGA[A/G/T]CAGGGGGAGGAAAAG | 6709 |
rs376861805 | snp | G/T | 1.65337e-05 | 0.00287517 | missense | SPTAN1 | GRCh38.p7 | 9:128584449 | TTCTCTGCGGTTGCA[G/T]CAGCTCTTCCGGGAT | 6709 |
rs376873836 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623881 | ACCTGAGGTCAGGAG[C/T]TCGAGACCAGCCTGA | 6709 |
rs376897533 | snp | A/G | 6.58979e-05 | 0.00573974 | missense | SPTAN1 | GRCh38.p7 | 9:128582737 | AGAGAGCCATGCGTC[A/G]CCGGGCCCAGCTAGC | 6709 |
rs376931503 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566403 | ATTATTTGAATACCA[A/C]AGTTGCTGTTTCCTC | 6709 |
rs376940683 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624711 | TCAATAAACAAAAGC[C/T]TGTAAACGCTGCTGC | 6709 |
rs376955753 | snp | A/G | 0.000131885 | 0.00811942 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609025 | GCCCTGAGAGGATGC[A/G]TCCCCTCATACGAAG | 6709 |
rs376957536 | snp | C/T | 1.6661e-05 | 0.00288621 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128583223 | GGATGAAGTGGCAGC[C/T]CGTATGAATGAGGTG | 6709 |
rs376973101 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557993 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 6709 |
rs376994715 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595732 | AACCCCAGTGGCCCA[C/T]GCAGCCACTCATCTG | 6709 |
rs377007713 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596750 | AGGGTAGAGGGCAGT[A/G]GATGATCATAGCTCA | 6709 |
rs377029920 | snp | C/T | | | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128550983 | TCCACTCCAATGGAG[C/T]GAGTGGGTAGGGAAA | 6709 |
rs377029946 | snp | C/G | 0.000347939 | 0.0131852 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605244 | GCAGAGTCTTCTGTT[C/G]TGCAGAGCATACCCC | 6709 |
rs377071017 | snp | C/G | 1.64874e-05 | 0.00287113 | missense | SPTAN1 | GRCh38.p7 | 9:128581003 | GAGCAGTGCATGGAC[C/G]TGCAGCTCTTCTACC | 6709 |
rs377113325 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578700 | TGGTCATGGTGGCAC[A/G]CGCCTGTAGTCCCAG | 6709 |
rs377119413 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597973 | TTGTTTTTGAGATGG[A/G]GTTTCGCTCTTGTTG | 6709 |
rs377129746 | snp | A/T | 3.29451e-05 | 0.00405851 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575195 | TCTTATGGTCCCTGA[A/T]TAGGAAGCAATTGTT | 6709 |
rs377163231 | snp | A/G | 0.000149042 | 0.00863128 | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633378 | TGCTTGCCCTGCGTC[A/G]CCTTGCTGCATGTCC | 6709 |
rs377172374 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557929 | CTGCCTCAGCCTCCC[A/G]AATAGCTGGGACTAC | 6709 |
rs377194470 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624309 | GGCTGACCAGTGTGT[A/G]CCTCTCTCCATGGCC | 6709 |
rs377221007 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595069 | CCTGCCTCAGCCTCC[C/T]AAAGTACTGGGATAA | 6709 |
rs377222137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622897 | AGCTGGGGTTACAGG[C/T]GCCTGCCACCACGCC | 6709 |
rs377241159 | snp | C/T | 1.66178e-05 | 0.00288247 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585724 | CGTAGTTTTTGTTAT[C/T]CTCTTTCCCTACCCA | 6709 |
rs377253398 | snp | A/G | 0.000214569 | 0.0103556 | missense | SPTAN1 | GRCh38.p7 | 9:128625934 | CTGGCCAACTCAGCC[A/G]CCCGCAAGAAGAAGC | 6709 |
rs377258326 | snp | A/G | 1.64779e-05 | 0.00287031 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574820 | TCAATGACAAGGCAC[A/G]TTTTGGGAAGAAGGG | 6709 |
rs377269806 | in-del | -/TTGGG | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602208 | TTTTTTTTGTTTTTT[-/TTGGG]TTTTTTTTGTTTTTT | 6709 |
rs377281314 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620035 | AAGCTGGCTAGACCA[A/G]CCTCCTTCAGCAGCA | 6709 |
rs377310637 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560580 | GAGACAGAATTTTAT[C/G]ACGTTGGCCAGGCTG | 6709 |
rs377318517 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128587686 | TTTGCGAGAACAAGC[A/G]CAGTCCTGCCGGGTA | 6709 |
rs377363051 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632391 | ACACAGTCACCTGCT[G/T]TGTGGAGGGTCTGTT | 6709 |
rs377366729 | snp | C/G | 1.64836e-05 | 0.0028708 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611856 | TCAAGGTATGGCCCA[C/G]CAGCTCCCGGTGCCC | 6709 |
rs377378707 | snp | A/G | 0.000153988 | 0.00877328 | missense | SPTAN1 | GRCh38.p7 | 9:128582845 | CCACAGATGAAGCTT[A/G]TAAAGTAATGTACTG | 6709 |
rs377381640 | snp | A/C | 1.64727e-05 | 0.00286986 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591461 | TTACTTTCAGTTCTC[A/C]CTCTTTTTTCCTTAG | 6709 |
rs377387388 | snp | A/C/T | 0.00102094 | 0.0225707 | missense | SPTAN1 | GRCh38.p7 | 9:128582731 | TTCACGAGAGAGCCA[A/C/T]GCGTCGCCGGGCCCA | 6709 |
rs377395236 | snp | C/T | 1.65149e-05 | 0.00287353 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605247 | GAGTCTTCTGTTCTG[C/T]AGAGCATACCCCCTT | 6709 |
rs377424316 | snp | A/G | 0.00036242 | 0.0134566 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578074 | CACCCTGGAACCTCC[A/G]CTGGAAACATAATGT | 6709 |
rs377437879 | snp | A/G | 0.000157198 | 0.00886422 | SPTAN1 | 9 | allele_origin=G(germline)/A(germline) | 9:128583291 | TGAAAGGTAAGAGAT[A/G]TTCCATTGAATTGTG | 6709 |
rs377443767 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565274 | CCATTGCACTCCAGC[C/G]TGGTGACTGAGCGAG | 6709 |
rs377444045 | snp | A/G | 3.29451e-05 | 0.00405851 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575153 | TGGAAGCCATTGTTA[A/G]CAAATGTTGGTTGGT | 6709 |
rs377449636 | snp | A/G | 0.000477984 | 0.015452 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617972 | GCTGTTAACCTCCTC[A/G]TCCTTGCCTGTCAGG | 6709 |
rs377452105 | snp | C/T | 0.000921575 | 0.0214462 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588992 | ACGCTGGCACCTCCA[C/T]GTATGCTCAGTTGGG | 6709 |
rs377488277 | snp | A/G | 1.66801e-05 | 0.00288787 | intron-variant, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633190 | GCTCAGGCACCAGGT[A/G]CCATCTCTTACCCCA | 6709 |
rs377521527 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630949 | CCTGACCTCGGCTGA[C/T]CTGCCCGCCTCGGCC | 6709 |
rs377553021 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571116 | AACATAGTGAGACCT[C/T]GTCTCTACAAAAAAA | 6709 |
rs377553316 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608111 | CCTCATTTTCTCACC[G/T]GCCTCTTGCCCTCTT | 6709 |
rs377593851 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567391 | CCACCTCCCAGGTTC[A/G]AGTGATTCTCCAGCC | 6709 |
rs377595045 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613688 | TGTAGGTTTTATCAA[C/T]GCTCACCATTATTAA | 6709 |
rs377595888 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574868 | AAAGAAAAGGGAAGA[A/G]ACTCCTCTGTGATCT | 6709 |
rs377597259 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595576 | GGGTAAATTCACAAA[A/G]CTAGCCATTTTAAAC | 6709 |
rs377659187 | in-del | -/AG | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606500 | TATTTTTTTTTTGGG[-/AG]GGGGGAAGCGTTTCG | 6709 |
rs377662829 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128552392 | CGCATTGTCGCTTCG[G/T]CTCCTTCCGGGATCG | 6709 |
rs377664159 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570567 | GGTCTTGAACTTCTG[A/T]CCTCAGGTGATCCAC | 6709 |
rs377690550 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612484 | ACATCCATAGGGAAG[A/G]CAAATAGGAAGAGAT | 6709 |
rs377714035 | in-del | -/TA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600288 | GTGATGCTTAATATA[-/TA]CAAAAGCAGAGTGTC | 6709 |
rs386416283 | in-del | -/TTT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560085 | ACATCCACCTCACCT[-/TTT]TTTTTTTTTTTTTTA | 6709 |
rs386416284 | in-del | -/TTT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560097 | CCTTTTTTTTTTTTT[-/TTT]TTAAGAGACAGAGTC | 6709 |
rs386416286 | in-del | -/TTT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588311 | ACTTTAAAATGAGAT[-/TTT]TTTTTTTTTTTTTTT | 6709 |
rs386416287 | in-del | -/TTT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588326 | TTTTTTTTTTTTTTT[-/TTT]TTGAGATGGAGTTTC | 6709 |
rs386416288 | in-del | -/TTT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594430 | TTTGAGTCTCTTGAT[-/TTT]TTTTTTTTTTTTTTT | 6709 |
rs386416289 | in-del | -/TTT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594448 | TTTTTTTTTTTTTTT[-/TTT]TTGAGATGGATTCTC | 6709 |
rs386738723 | multinucleotide-polymorphism | CT/TC | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578595 | CAGCACTTTGGAAGG[CT/TC]GAGGCGGGTGGATCA | 6709 |
rs386738724 | multinucleotide-polymorphism | CA/TG | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579363 | GACAGAGCCCTGGAA[CA/TG]AAAGAGAGCTCAGAC | 6709 |
rs386738725 | multinucleotide-polymorphism | AG/TT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624116 | AAAAAAAAAAAAGAA[AG/TT]CCTAAAAGTAGAATT | 6709 |
rs397703368 | in-del | -/A | 0 | 0 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571302 | AAAGAAAAAAAAAAA[-/A]GGCCAGGCACAGTGG | 6709 |
rs397733958 | in-del | -/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577890 | GGGACAGGATTGGGG[-/G]CATTATAGTGATGGA | 6709 |
rs397759299 | in-del | -/A | 0 | 0 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599706 | AAAAAAAAAAAAAAA[-/A]GTCTTCTGTCTCTTC | 6709 |
rs397779794 | in-del | -/AGA | 0 | 0 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128550881 | TTTTCTCTACATAGA[-/AGA]TTGCAGGAAATGCCT | 6709 |
rs397817905 | in-del | -/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630626 | CTCCACCTCCCAGGT[-/T]CAAGCAATTCTCCTG | 6709 |
rs398012350 | in-del | -/A | 0 | 0 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581488 | CAAAAAAAAAAAAAA[-/A]CAAACAAAAAAAACA | 6709 |
rs398012351 | in-del | -/T | 0 | 0 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592292 | CTTTTTTTTTTTTTT[-/T]GAGACAGATTCTCGC | 6709 |
rs398012352 | in-del | -/A | 0 | 0 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606007 | CAAAAAAAAAAAAAA[-/A]TTAAAAACAGAAAAA | 6709 |
rs398113914 | in-del | -/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586833 | TTTCTTTTTTTTTTT[-/T]CTGAGACAGAGTCTC | 6709 |
rs398122865 | in-del | -/AGC | | | cds-indel | SPTAN1 | GRCh38.p7 | 9:128627414 | AGCTGCAGAAGGAAC[-/AGC]GGCGGCAGGAGGAGA | 6709 |
rs431905519 | in-del | -/TG | 3.34703e-05 | 0.00409072 | SPTAN1, WDR34 | 9 | allele_origin=G(germline)/(germline) | 9:128633813 | TTGTTCCGTGAACTC[-/TG]TGCTCAGCTGCCACA | 6709 |
rs527246009 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565692 | CTCTTAGCCTACTCA[-/C]CCTTTTCTTTCTGTC | 6709 |
rs527280059 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588207 | TTCACTATGTTGGCC[A/G]GGCTGGTCTTGAATT | 6709 |
rs527295113 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557154 | ATGACCAAACGACCC[A/G]TTCATCCTGTTAGTC | 6709 |
rs527376488 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622060 | AGACTAGGGTTTGAT[A/C]CATAGGCAGCAACAA | 6709 |
rs527389671 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568597 | AGAGGACCAGGAGAA[A/C]TGCAGTCAGAGTATT | 6709 |
rs527496623 | snp | A/G | 4.94556e-05 | 0.00497246 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628029 | CTTGTGGAGGATCCC[A/G]GGATGGGCCTTCCTG | 6709 |
rs527530951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583480 | CGAGCATACTGGTTG[A/G]TGAGGGAGTCTGAGT | 6709 |
rs527545517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588516 | GGGTTTCTCCATGTT[A/G]GTCAGGCTGGTCTCG | 6709 |
rs527551774 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595261 | ATTACAGGTACGCAC[A/G]ACCACATCTGGCAAA | 6709 |
rs527570862 | snp | C/T | 1.68071e-05 | 0.00289884 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632952 | CAAGGAGGAGCTCTA[C/T]CAGGTATGGGCCTCA | 6709 |
rs527584454 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621933 | ACTCAGGTGCAGTGA[C/T]GCACCTGGAGTGCCT | 6709 |
rs527608187 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589082 | TCCTCACCAATCCCC[C/G]ACGTGACATACATTT | 6709 |
rs527638561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628988 | GAACCACTGGGCCTG[C/T]TGCCTCCAGGTACCC | 6709 |
rs527640924 | in-del | -/TTTA | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602637 | TGTTTTTATTTGTAT[-/TTTA]TTTATTTATTTTCGA | 6709 |
rs527664774 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584904 | TCTCCCCTTCTTGCC[A/G]AGGGCATGGCCACGT | 6709 |
rs527701297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623414 | TTTTTTCTATCAAAA[A/G]TAATACTAATGAATA | 6709 |
rs527742392 | snp | C/T | 0 | 0 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590524 | ACCTGGGGCACATAG[C/T]GAGACCTCATCTCTA | 6709 |
rs527776270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628511 | GCACCCGTTATGTGA[C/T]AGACAGGACGTGGGA | 6709 |
rs527909305 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625515 | GCAGGGCGAGTGTTC[-/T]GGGCAGAGCTGGCAG | 6709 |
rs527910558 | snp | C/G | 1.68279e-05 | 0.00290064 | downstream-variant-500B, missense | SPTAN1, WDR34 | GRCh38.p7 | 9:128633880 | AGCTGAGTCTGCTGG[C/G]TGTTGAACTCCAGAC | 6709 |
rs527956773 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602225 | GGGTTTTTTTTGTTT[G/T]TTTTTTTTTGAGACA | 6709 |
rs527972851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128555504 | TCCAAAGAAAGGGGG[A/G]AAAAAACCCTGCCTG | 6709 |
rs528020478 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622331 | TGCGACGGAGTTTCG[C/T]TCTTGTTGCCCAGGC | 6709 |
rs528070932 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591772 | TTTGAGCCCACAGAC[C/G]TCCCTGTGTGGGTCT | 6709 |
rs528142436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604148 | CTGTCAAGCACAGCT[A/G]GTTTTGGCTTGGCTC | 6709 |
rs528155510 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | SPTAN1, WDR34 | GRCh38.p7 | 9:128633677 | AGCTTTGCTTTTCTT[C/T]ATTTGGCTTGCGTCA | 6709 |
rs528191002 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557866 | TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG | 6709 |
rs528243910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563686 | ATCTGCAACATTCAG[C/T]ATGGACTTGATCATT | 6709 |
rs528258943 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571360 | GAGGCTGAGATGGGC[A/G]GATCATCTGAGGTCA | 6709 |
rs528275412 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | SPTAN1 | GRCh38.p7 | 9:128603543 | TTCCTCCCTACCTAG[C/T]CTGCTCGTCTGATGG | 6709 |
rs528354428 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617363 | ATATAATTTGATAGG[G/T]CTCCTCAGGGCAGCA | 6709 |
rs528406698 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570604 | CAGCCTCCCGAAGTG[C/G]TGGGATTACAGGCTT | 6709 |
rs528428177 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606086 | GTTAAAAATAAGTCT[A/C]TGCAGCCGGGCACGG | 6709 |
rs528453768 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626874 | GGCTTCAGTGCAGTG[C/G]TGCTACCATGGCTCC | 6709 |
rs528488428 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629278 | CCTGACTAACCTGCC[A/G]CCCTCGGCTGCTTGG | 6709 |
rs528499842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605686 | CTATTTCTATTATAA[A/G]ATTTTAATTTAAAAA | 6709 |
rs528500533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559643 | ATGTTTTTCCATCTT[A/G]ACTGTTTCCTGAGGG | 6709 |
rs528589042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565257 | AGTGAGCTGAGATCA[C/T]GCCATTGCACTCCAG | 6709 |
rs528654766 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598244 | TGAGCCACCATGCCC[C/T]CAGCCATAGCTTATT | 6709 |
rs528670071 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563528 | TTGTGTAGCTTTAGT[A/C/G]AGCACATTCTTTATT | 6709 |
rs528670255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625244 | GAGATGACTGGTGGC[A/G]TCTTTCACTGAGGCA | 6709 |
rs528686294 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618455 | CCATGGACGGCCTGA[C/G]TGACTGTGAGGGCTC | 6709 |
rs528691072 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566292 | GAACTCCTGGAGTCA[A/G]GCAGTCTGCCACTTT | 6709 |
rs528729187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572304 | AGGCTTGCTTGTCCA[C/T]CCCGTCAGCTTTCCA | 6709 |
rs528752928 | snp | C/G | 8.26644e-05 | 0.00642848 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128585776 | AGAGGATGTGAAGGC[C/G]AAGCTTCACGAGCTG | 6709 |
rs528805392 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624709 | GGTCAATAAACAAAA[A/G]CCTGTAAACGCTGCT | 6709 |
rs528814536 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586372 | TCCTGGCCTCAAACA[A/T]TCCTCCTGCCAAAGC | 6709 |
rs528840223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581974 | AGGATTCCAAACAGA[C/T]TTGATGAAAGATTCA | 6709 |
rs528844053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573777 | CTTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGTC | 6709 |
rs528904599 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620817 | TGGGTGTATATCTTC[A/T]GCTTGCTTTGTGTCA | 6709 |
rs528905272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574557 | TTTAGGGATTATCTT[C/T]TAAAAATATTTTTAT | 6709 |
rs528914856 | in-del | -/TTTG | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630697 | CACATTTGGCTAATT[-/TTTG]TTTATTTTTAATTAT | 6709 |
rs528966219 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560843 | CCAATATGGTGAAAC[C/T]CAATCTCTACAAAAG | 6709 |
rs528967269 | snp | C/T | 1.67217e-05 | 0.00289147 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632315 | CCTGGAGCAGCAGAT[C/T]CAGGCCAGGTACCCG | 6709 |
rs528987011 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588791 | TTTACCATGTTTGCC[C/T]TTCCTTTGGATTTTT | 6709 |
rs529000922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588206 | TTTCACTATGTTGGC[C/T]GGGCTGGTCTTGAAT | 6709 |
rs529043556 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626897 | ATGGCTCCCTGTAGC[C/G]TCAACCTCCCAGGCT | 6709 |
rs529078876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593908 | TGGTTGTGTTGTTCT[A/G]AGTGCAGAATCGGCC | 6709 |
rs529125437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631862 | GCTTCCTGGAGTCCT[C/T]GCCGTACTTGTCCTT | 6709 |
rs529147617 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128551794 | GAATGTAAGAAATTA[C/T]TATTTTGCCGCTGCC | 6709 |
rs529205496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593219 | CGGTGCAGCTGTGTC[A/G]GTCGATGACTGCTTA | 6709 |
rs529246569 | in-del | -/TT/TTT/TTTT | 0.255224 | 0.249945 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588310 | TACTTTAAAATGAGA[-/TT/TTT/TTTT]TTTTTTTTTTTTTTT | 6709 |
rs529264666 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128555155 | GACCTGGGAACCTTG[C/G]TTCTCCTTCCACATT | 6709 |
rs529303564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601436 | TGACTTTATAAAAGT[A/G]GATCTTTTGGCTAGG | 6709 |
rs529363918 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595299 | ATTTTTAGTACAACC[A/G]GGATTTTGCCATGTT | 6709 |
rs529403611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554397 | TGTAAGCCTGTCAAG[C/T]AATATGATGAAGAGG | 6709 |
rs529441302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568415 | TTGAGAAAACTGTTG[A/G]TATGGTTCTGTATTT | 6709 |
rs529458809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607206 | ACAGGGTTGCACCAC[A/G]TTGCCCAAACTGATC | 6709 |
rs529462203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561134 | CAGCACTTTGGGAGG[C/T]CGAGGCGGGCGGACC | 6709 |
rs529492181 | in-del | -/TTTG | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596273 | GTTTTGTTCGTTTTT[-/TTTG]TTTGTTTGTTTGTTT | 6709 |
rs529552362 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565898 | AGAGACTTGAGAGCA[C/T]GTCGTTTTTCCTGAC | 6709 |
rs529559638 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614077 | AGTTTTACACAGGTA[A/G]GTAGGTAGAAAAGGG | 6709 |
rs529575375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606659 | CGGCTAATTTTGTAT[C/T]TTTTTTAGTAGAGGC | 6709 |
rs529583158 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621372 | AACCAAGGTCTGCGT[C/G]GAGACCAGCAGCAAT | 6709 |
rs529592062 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614613 | AACAAAAAAAAAACA[A/C]AAAAATTAATTAGCC | 6709 |
rs529632119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562801 | AACGCCATCTCTACT[A/G]AAAAATAGAAAATAT | 6709 |
rs529693203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128556505 | AACTTAAATACCTCT[C/T]ATCTGAATTTTGCAG | 6709 |
rs529701289 | snp | A/G | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128553431 | AGCGTTCTTGTTTGT[A/G]TGTGTGTTTCCTGGG | 6709 |
rs529723191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616553 | GGGCAGATCACTTGA[A/G]GTCAGGAGTTCGAGA | 6709 |
rs529785438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608683 | TTGAGTTAAACTCTA[C/T]TCTAGTAATGAATGA | 6709 |
rs529798313 | in-del | -/AAAAAAA/AAAAAAAA | 0.0581099 | 0.160244 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606374 | GCAAGACTCTGCCTC[-/AAAAAAA/AAAAAAAA]AAAAAAAAAAAAAAA | 6709 |
rs529809477 | in-del | -/AAACAAAT | 0.371582 | 0.218444 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564576 | AAGGTCCTGTCTCAA[-/AAACAAAT]AAACAAATAAATAAA | 6709 |
rs529825622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569939 | ATTAACTATTACTAA[C/T]AATGATGATTGTAAA | 6709 |
rs529827109 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610650 | TGTGGCATAGCTGCT[A/G]TGTCCTTGCAATTGT | 6709 |
rs529846719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622738 | TGACTTGTAGTATGG[C/T]TTATTTATTTATTTA | 6709 |
rs529854221 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580309 | ATAAATAAAAATAAA[A/G]TATGTATATATATAC | 6709 |
rs529881462 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584190 | GCAGAAAGAATCCTC[G/T]CAGGAATGGAAAAAA | 6709 |
rs529891767 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575798 | GGCTCTCCACTCTGG[C/T]GCTGGAGCCCATTAA | 6709 |
rs529904905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589749 | CCCGGCTAATTTTTT[A/G]TATTTTTAGTAGAGA | 6709 |
rs529925824 | snp | C/T | 1.6786e-05 | 0.00289702 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628065 | GGCGGGCTGCACTTC[C/T]CCTCCCACCCTTCTC | 6709 |
rs529962403 | snp | C/T | 0.000691984 | 0.018588 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576976 | CAAGCCAGAGTGGGC[C/T]TTGGGGAATGGGTCT | 6709 |
rs529964955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569199 | AGATGGCAGAGCATA[C/T]TAGTGAAATTGGCAA | 6709 |
rs529981376 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622169 | AGCTACAGCCATGTA[G/T]AGATGTAGACGTGGC | 6709 |
rs529985786 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628469 | GGGAGGGTAACAAGA[C/G]TGTCCGCCCTAATAG | 6709 |
rs530123587 | in-del | -/TA | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602345 | CCTCAGCCTCCCGTG[-/TA]GCTAGGATTACAGGC | 6709 |
rs530212688 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616802 | CTGGGCATGGTGGCA[C/T]GTGCCTGTAATCCCA | 6709 |
rs530213914 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591187 | CTGCATCAGCCTCCC[G/T]AGTAGCTGGGGCTAC | 6709 |
rs530216170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585514 | CTAATGCCAACTTGC[A/G]ATATCTGCTTCTTAG | 6709 |
rs530252227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629081 | AGTGTGCTCTTGCCT[C/T]CCCTCCCTTTGGTGT | 6709 |
rs530272601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584964 | ATACCATCCCCATTC[C/T]TTCCTAACTGTATGA | 6709 |
rs530361602 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128591530 | TGTGCCGGCTGCGTA[C/T]GTGAAGAAATTGGAC | 6709 |
rs530372325 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596512 | TGATCTCCTGACCTC[A/G]TGATCCACCCGCCTC | 6709 |
rs530405234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586466 | ATGAAAATGTAATCA[C/T]ACCTAAAGGAGAGAG | 6709 |
rs530473527 | snp | C/T | 1.64743e-05 | 0.00287 | missense | SPTAN1 | GRCh38.p7 | 9:128600087 | TTGAATAGGATGAAA[C/T]TGATTCCAAGACAGC | 6709 |
rs530477553 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598148 | GGACAGGGTTTCTCC[A/G]TGTTGGTTAGGTTGG | 6709 |
rs530479372 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128551455 | TCCTATTTGAAGGCA[A/G]TACACATACGGTTGC | 6709 |
rs530548615 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631034 | ATTTTTAGTAGAGAC[A/C]GTGTTTTGCCTTGTT | 6709 |
rs530571534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558083 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 6709 |
rs530641724 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610154 | AGAACTGTAGAGAGA[C/T]GGATGGTCTATTAAT | 6709 |
rs530689469 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610365 | AGAAGAAGAGGGTAA[G/T]GGGACTTTTGTCAGG | 6709 |
rs530723680 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572003 | CCGGCACCACAGGAA[A/C]GCACAAGCACACTGA | 6709 |
rs530747985 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604219 | TTGGAAACAGGAAAT[G/T]ATATATGCCCTAGCA | 6709 |
rs530770826 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558595 | GGCTGGTAAGATTGG[A/T]GTTTGTTTTTTAATG | 6709 |
rs530774464 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596433 | AGGCACCCGCCACCA[C/T]GCCCGGCTAATTTTT | 6709 |
rs530795999 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618194 | TGGGGGTCCAGTGGG[A/C]CCTCCTACTGTCTCC | 6709 |
rs530807829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606570 | CTCACCGCAACCTCC[A/G]CCTCCTGGGTTCAAG | 6709 |
rs530861133 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575440 | TTGGTCCCCTAATTT[C/T]TGAGTGAGCAAGTTT | 6709 |
rs530868477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611261 | GATTGCTTGAGCTCG[A/G]GAGTTCAAGACCAGC | 6709 |
rs530884909 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560236 | TTACAGGCGCACGCC[A/G]CCACACCTGGCTAAT | 6709 |
rs530890772 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562740 | GAGGCCAAGGTGGGC[A/G]GATCACGAGGTCAGG | 6709 |
rs530895735 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633401 | GCATGTCCGCTCCTC[C/T]GTGTGCTCTCACTTT | 6709 |
rs530917745 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599771 | GTTCATTTATTACCC[C/G]TTTGCAGACAATCTT | 6709 |
rs530931678 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596239 | TTTGATACACTACAC[A/G]TTGTTTTTGGGTTTT | 6709 |
rs530946071 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566504 | TTCCTTGCCGTGTGT[A/G]GGTTAGGCATCTTCT | 6709 |
rs530949690 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128552580 | GAGGCGGGGCGCGCG[C/T]GTCGCCGCCACTACC | 6709 |
rs530979806 | snp | A/G | 1.6513e-05 | 0.00287336 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581085 | AGCAAAGCCTTGCCA[A/G]TGGTGGGAGAAGAAG | 6709 |
rs531007000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613318 | CACTGGGCAACCTGA[A/G]TTTTCCAGAATGCTG | 6709 |
rs531021078 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619742 | ACTTCACCATCTCTT[C/G]AGGGGGACACAGTTC | 6709 |
rs531070254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606094 | TAAGTCTCTGCAGCC[A/G]GGCACGGTGGCTCAC | 6709 |
rs531119989 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128552070 | ACGCACTCGGGTGAT[C/G]TCACCCTTTGGGACT | 6709 |
rs531154956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573675 | TGGCCAGGCTGGTCT[C/T]GAACTCCCGACCTCC | 6709 |
rs531156296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619122 | AGCACACAGGGCCAG[C/T]AGCCAAGGCCTCAGT | 6709 |
rs531209471 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585429 | AAAGAGCTGATAGAG[C/T]GCCTGCACGTGCCAG | 6709 |
rs531242026 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580503 | TGTCATTAGTAGCTT[C/T]GGAGCCTAAAGTCTA | 6709 |
rs531269734 | snp | A/C | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128553355 | TGTGATTTGCTTGTA[A/C]ATAATAGGTAAATGC | 6709 |
rs531279503 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620714 | TAGAGCAAGAACTCC[A/G]TCTCAAAAAGAAAAA | 6709 |
rs531312126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574583 | TTTATTCAGCGCTCC[A/G]TAAGGTCTCTAACTT | 6709 |
rs531323333 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593898 | CAGTCCCTTGTGGTT[G/T]TGTTGTTCTAAGTGC | 6709 |
rs531329976 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580132 | ATCCTGAACAACATA[A/G]TGAGACCCCCATCTG | 6709 |
rs531344103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614768 | TGACAGAGCAAGGAA[A/G]AAAAAGTTGTTGGGG | 6709 |
rs531469849 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588152 | ACTGGCGCCCGCCAC[C/T]ACGCCCAGCTAATTT | 6709 |
rs531482649 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128553328 | TAATAAACATTTTTC[G/T]TTCTTCCTAGTTGTG | 6709 |
rs531487423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632400 | CCTGCTGTGTGGAGG[A/G]TCTGTTCCCTAATTT | 6709 |
rs531510310 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588389 | TGATCTTGGCTCACC[A/G]CAACCTCCGCCTCCC | 6709 |
rs531548428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626962 | TGGGACTACAAGCAC[A/G]TGCCACCACGCCTGG | 6709 |
rs531584960 | in-del | -/A | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617238 | ATGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAGT | 6709 |
rs531625763 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628501 | AGGCAAAAATGCACC[C/T]GTTATGTGATAGACA | 6709 |
rs531644861 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595925 | CTCGGCTTACTGCAG[C/G]CTCCGCTTCCTGGGC | 6709 |
rs531646475 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584208 | GGAATGGAAAAAAGA[C/G]CTTATCAATTTTTCT | 6709 |
rs531687124 | snp | G/T | 0.000503501 | 0.0158587 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628096 | GTCACCTGATGAGGA[G/T]TGTGTGCCTTGCCCC | 6709 |
rs531810938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602208 | TTTTTTTTGTTTTTT[C/T]TGGGTTTTTTTTGTT | 6709 |
rs531818719 | in-del | -/C | 0.0142736 | 0.0832652 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588088 | CTGCAACCTCTGCCT[-/C]CCAGGTTGAAGCAAT | 6709 |
rs531872531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569026 | GAATTTATGAAGTCT[C/T]CTTAAGAAGTTACCC | 6709 |
rs531885782 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554556 | ATAGTCCCCCATGTC[C/G/T]TGTCACTGCTGAATC | 6709 |
rs531938626 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611199 | TTTTGGCCAGGCTTG[C/G]TGGCTCATGCTTGTA | 6709 |
rs532012044 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596976 | ACTAGCCTGGCCAAC[A/G]TGGCAAAACCCCATC | 6709 |
rs532022297 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561611 | GAGCTTGCAGTGAGC[C/T]GAAATTGCACCACTG | 6709 |
rs532057870 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615444 | GTGCAAATGTCCACA[C/T]GGTAAAAAATAATAA | 6709 |
rs532133375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603473 | GGACCTAATCAATGA[C/T]ACTTGCAGCTCAGAT | 6709 |
rs532134180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604019 | GCTGTGACTTAGGAA[A/G]CAGTTGCTACCTGCC | 6709 |
rs532216090 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128553033 | TCCGGCTGCGGCAGG[G/T]GGGTGGGGGCTCCCT | 6709 |
rs532282547 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622765 | TTTATTTATTTATTT[A/T]TTTTTTAGACGGAGT | 6709 |
rs532297319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577820 | AGGATTAGAAAGGAA[A/G]AGAATCCTTGCTAGC | 6709 |
rs532313408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570047 | AATTAAATACAGATA[C/T]TTATCTTCCCATCTT | 6709 |
rs532379181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570755 | TCCACCTCCCAGTTT[C/T]AAGTGATTCTCCTGC | 6709 |
rs532399096 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565185 | GTGCAGGCCTGTAGT[C/G]CCCGCTACTCGGGAG | 6709 |
rs532503316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571518 | TGAACTCAGGAGGCG[A/G]AGGTTGAAGTGAGCC | 6709 |
rs532504205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572159 | GCCACTGCACCCAGC[C/T]TGTGTGCTTTATTTT | 6709 |
rs532532127 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572801 | CCCATAGTCACCGCC[A/T]CCCACATCGGGTCCC | 6709 |
rs532552554 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629715 | GCTCCCTCCCTGGCT[G/T]TGTCTAGAGGATGGA | 6709 |
rs532553801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611427 | GTGAGCTGAGATTAC[A/G]CCACTGCACTCCAGC | 6709 |
rs532597370 | in-del | -/T | 0.26518 | 0.249539 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563716 | TTATTCAACCATTTC[-/T]TTTTTTTTTTTTTTT | 6709 |
rs532628384 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617834 | AGACAAACCCCTTGC[A/G]CTTATTTCACTGAGG | 6709 |
rs532729245 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585641 | GGGCACAGCTCACCA[A/C]AACATAGTAATGAAA | 6709 |
rs532747651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625543 | CAGGGATCCCTGGGG[C/T]GGGAGAGCGGAAGGC | 6709 |
rs532777504 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580601 | GTCCCTACTCCATTT[A/C]TACTCCATTAAACTC | 6709 |
rs532791007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597694 | TGCTCTGTTGCCCAG[A/G]ATGGAGTGCAGTGGC | 6709 |
rs532826227 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593169 | GAGGAACTGCCTGTC[C/T]GTGCAGCAGCTTTGG | 6709 |
rs532868933 | snp | A/G | 9.97175e-05 | 0.00706037 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591671 | AGGCGTCCCATAGGC[A/G]TACTCTGTTCCACAT | 6709 |
rs532907911 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631776 | CAGTGAGCGTGATTG[C/T]GCCACTGCACTCTAG | 6709 |
rs532908765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593829 | CAGCAAGTTCATCTC[A/G]TCTCTCCACTGTAGT | 6709 |
rs532915283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559617 | AAACAAATTAGATGC[A/G]TAATTTCTCAATGTT | 6709 |
rs532938793 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128550626 | TTCACTATGGGGCCA[C/G]GGTGATTTAATAGAA | 6709 |
rs532953851 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559932 | TAGAGATGGGGTTTC[A/G]CCATGTTGGCCAGGC | 6709 |
rs532966260 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562422 | TGTATGATATTAGAT[A/G]GTAGGGTTGGGAGTG | 6709 |
rs533042543 | snp | A/G | 0.000362528 | 0.0134585 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128605076 | TGAAGAGAAGAATCA[A/G]GCTCTAAACACAGAC | 6709 |
rs533149499 | snp | C/T | 0.000131802 | 0.00811688 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599021 | TGTGGATCTTGAACA[C/T]GAGAAGGACTTAAAT | 6709 |
rs533168287 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128551654 | ACACGAAATACTTAG[C/T]ATAGTGCCTAGTACA | 6709 |
rs533170856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601240 | CACCTGCCTCGGCCT[C/T]CCAAAGTGTTGGGAT | 6709 |
rs533225969 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612306 | TCATTTGGCACAGTG[A/G]GTCCATCAGTGCCCA | 6709 |
rs533266050 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565693 | TCTTAGCCTACTCAC[A/C]CTTTTCTTTCTGTCT | 6709 |
rs533283721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605586 | CAATGGCTCACACCT[A/G]TAATCCAAGCACTTT | 6709 |
rs533315137 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128553639 | GTTAAAAGTTGAATA[A/T]GTTTTAAATGAAAAG | 6709 |
rs533329807 | in-del | -/A | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612924 | GCGAGACTTCATCTC[-/A]AAAAAAAAAAAATTT | 6709 |
rs533351094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614006 | CAAGACTCCATCTCA[A/G]AAAAAAAAAAAAATG | 6709 |
rs533353031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606110 | GGCACGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 6709 |
rs533360315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594733 | TTCTGCGCCTGGCCA[A/G]AGTCTCTTGATTTCT | 6709 |
rs533383147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554311 | ACTGATTCTCTGATA[C/T]GCTTTGGTCTTGGCA | 6709 |
rs533390578 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567454 | CTGCCACTGTGCCCA[C/G]CTAATTTTTGTATTT | 6709 |
rs533458316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561097 | TATGTCGGCCAGGCA[C/T]GGTGGTTCACGCCTG | 6709 |
rs533502812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600496 | GCCTGGCCTCTTTAT[C/T]CTGTGGCCTAAGAAA | 6709 |
rs533528213 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622814 | CTGGAGTGCACTGGC[A/G]CAATCTCACCTCACT | 6709 |
rs533556414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128556289 | TTTGTTTTCTAAGTC[A/G]GACCTTTTTCACAAA | 6709 |
rs533589980 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589085 | TCACCAATCCCCCAC[A/G]TGACATACATTTATG | 6709 |
rs533591966 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577996 | ATTTCCCAGAATTAG[A/C]ATTTATATAGTTTGT | 6709 |
rs533599225 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626264 | AGACAGGAGCAGAGG[C/G]GAGCTAAGCTCCCAG | 6709 |
rs533650456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561304 | CTTGACCCTGGAGGC[A/G]GAGGTTGCAGTGAGT | 6709 |
rs533653202 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616767 | TCAAAAAAATAAAAA[-/AT]ATAAAAATATAAAAA | 6709 |
rs533686948 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573725 | TTCCAAAGTGCTGGG[A/T]TTACAGGAGTGAGCC | 6709 |
rs533716443 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557641 | TACCAAGAACTGCCT[C/T]AAACAGCTGTCTCTT | 6709 |
rs533717545 | snp | C/T | 4.94564e-05 | 0.0049725 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128568819 | TGAAGTGCAGGCCAA[C/T]TCAGGAGCCATTGTT | 6709 |
rs533790008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594989 | TAGTTTTTGTATTTT[C/T]AGTAGAGATGAGGTT | 6709 |
rs533790991 | snp | A/T | 0.0368353 | 0.130617 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568068 | CACTCGGCCAAAACT[A/T]TTTTTATAAAAAGGG | 6709 |
rs533803132 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597005 | TCTCTGCTGAAAATA[C/T]AAAAATTAGCTGGGC | 6709 |
rs533819057 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620759 | TGGAAGGCCTTTTCT[A/G]AGATGTGTTCAAGTT | 6709 |
rs533851962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606878 | TTTAATGTATTCACG[A/G]TGTTGTGCAGCCACC | 6709 |
rs533930456 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613711 | ATTATTAAAAATTAC[A/G]TAAATTTTAAGGCCA | 6709 |
rs533931801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600854 | TTTTAGTAGAGACAG[A/G]GTTTCGCCATGTTGG | 6709 |
rs533995158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614452 | AAAAAATTAGCAGGG[C/T]GTGGCATGTGCCTAT | 6709 |
rs534019227 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622323 | TTTTTTTTTGCGACG[G/T]AGTTTCGCTCTTGTT | 6709 |
rs534057878 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576419 | CAGGGACAAACTCTT[C/G]AGCCCCGAAAATTAT | 6709 |
rs534112706 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573946 | TTTTAGTAGAGATGG[C/G]GTTTCACCATGCTGG | 6709 |
rs534232787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562393 | GGCGTGAGCCACCGC[A/G]CCCAGCCGAGATCTG | 6709 |
rs534242435 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570152 | CCCAGAGTGAATGAG[A/G]CACCTCTGTAGTAGA | 6709 |
rs534260962 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575680 | GTGAATGCTAAGTTA[A/G]TATTGGCAGATGTCC | 6709 |
rs534281965 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629283 | CTAACCTGCCGCCCT[A/C/T]GGCTGCTTGGGAAGG | 6709 |
rs534336752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623702 | TGGTCTTGAACCCCT[A/G]GCCTCAAATGATCTG | 6709 |
rs534337161 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612378 | AGAAACCCTTATTAT[A/T]TATGAGTTGCATGCT | 6709 |
rs534349825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627779 | AGCCATGACTTGGTG[A/G]CAGACGATGCAGGGT | 6709 |
rs534477720 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564821 | GCAAAGAAGAGTCAT[A/G]GGACATTCTAAACAA | 6709 |
rs534497861 | snp | A/T | 8.51013e-05 | 0.00652253 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611696 | CTGGTTTGGAAAAAA[A/T]TTTTTTGGTATTTTT | 6709 |
rs534525127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596599 | TACACATTGTTTATC[C/T]ATTCCACCACTTAAA | 6709 |
rs534541618 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629062 | CTTTGTGTGTGTCTG[C/T]TGCAGTGTGCTCTTG | 6709 |
rs534551977 | snp | C/T | 0.00398564 | 0.0444627 | downstream-variant-500B, intron-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128634144 | CATGTGTGGTCTTTT[C/T]CCCAACCCAGAACCC | 6709 |
rs534573048 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628127 | ATAGCCCATGGTCCC[C/T]GGTCCCCGATAGAGC | 6709 |
rs534597852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585226 | TAGAGACAGGGTTTC[A/G]CCATATTGGTCAGGC | 6709 |
rs534670019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589614 | AATGTCTTGCTCTGT[C/T]GTCCAGGTTGCAGTG | 6709 |
rs534684507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597028 | AGCTGGGCGTGGTAG[C/T]GCCTGCCTGTAGACC | 6709 |
rs534728242 | in-del | -/AC | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558364 | ATTTTGCAAATATAT[-/AC]CTTTTTTTTTAAGTT | 6709 |
rs534731851 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128550909 | TGCCTCTCAGCTCCT[A/G]CGTTTCTCCTACACA | 6709 |
rs534742497 | snp | A/G | 0.000345875 | 0.013146 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584685 | CTGACTTTTCTCTTC[A/G]TGGTTGGATAACTGG | 6709 |
rs534747627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591318 | TAATCCACCCGCCTC[A/G]GTCTCCCAAAGTGCT | 6709 |
rs534755304 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597208 | AGAGATAGGGGTCTG[G/T]TTATGTTGCCCTAAG | 6709 |
rs534765749 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599857 | TTTCTTCTACTGGAT[-/A]AAAAAATTGGAATTT | 6709 |
rs534890676 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564105 | CTATCAAAACCCTGT[C/G]TCTACAAAAAAAATT | 6709 |
rs534923448 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563111 | GTTTTAAGGACTTGA[C/T]GTCTGTTTTAAGAAT | 6709 |
rs534969892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624259 | AGTTTAGAGCCTTTC[C/T]AGGGAGGGCATAGTC | 6709 |
rs534989164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617513 | GGCTTTTGTTGTTCA[A/G]AAAACTGGCAAGGAT | 6709 |
rs535010803 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598342 | AGTTTGTGACTATGT[C/G]TCCTTTGACTTTGGC | 6709 |
rs535031542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571113 | GGCAACATAGTGAGA[C/T]CTCGTCTCTACAAAA | 6709 |
rs535037140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592508 | TCAAACTCCTGACCT[C/T]GTGATCCGCCCGCCT | 6709 |
rs535052909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609766 | TCACACGGTTTGCTG[A/G]TGTCTCTTCATCCAT | 6709 |
rs535113572 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613554 | ACTCCTAAGGAAAAC[A/G]AGCGTGTTTGAGAAA | 6709 |
rs535138339 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580804 | TCCCCTTTTGCAAAT[C/T]GGAAAAAAGGCCTGA | 6709 |
rs535152254 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567092 | ATTGGACAAGAAGAA[C/T]ATAATAAGGAAGGAC | 6709 |
rs535196413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573390 | GTCTTTTCACAGAAG[A/G]TCCAAAGTTTTTTCT | 6709 |
rs535207456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571581 | CAAGAGCGAAATTCT[A/G]TCTGAAAAAAGTAAA | 6709 |
rs535272801 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564572 | AAAATAAGGTCCTGT[C/T]TCAAAAACAAATAAA | 6709 |
rs535286853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587110 | ACAGGCGTGAGGCAC[C/T]GCGCTCGTTCTGTCG | 6709 |
rs535380082 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567569 | GCTGGGATTACAGGC[A/G]TGAGCCACCACACCT | 6709 |
rs535438808 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620066 | TTCAGACAGGCAAAG[C/G]CAGGAGCTGCAAGAT | 6709 |
rs535534592 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594871 | CTCTCTTTTGTCGCC[C/T]AGGCTGGAGTGCAAT | 6709 |
rs535552825 | snp | C/T | 4.36958e-05 | 0.00467397 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626724 | GGAGCTGCTCGGCCT[C/T]CCAGAGCCCTCTCTG | 6709 |
rs535572913 | snp | A/G | 0.00296608 | 0.0383959 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632548 | AGGGCTGCCTGCTGA[A/G]CCGCCCTCGGCTTTG | 6709 |
rs535582336 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612937 | CTCAAAAAAAAAAAA[A/T]TTTTTTTTTTAATAA | 6709 |
rs535592754 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630733 | TTTGAGATGGAGTTT[C/T]ACTCTTGTTGCCCAG | 6709 |
rs535606844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624892 | AATAGCAACTGAACT[A/G]GAAGACGGGCTGCAG | 6709 |
rs535621149 | snp | C/T | 0.000164715 | 0.0090736 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603495 | AGCTCAGATCTCTAA[C/T]TGCCAGACACTTGAT | 6709 |
rs535656251 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596894 | GCCGGGCCCAGTGGC[G/T]CATGCCTGTAATCCC | 6709 |
rs535695259 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592765 | GCATGGCAGACCCGC[C/T]AGGAAAATGAAGGTG | 6709 |
rs535719471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606169 | GAGGTCAGGAATTCA[A/G]GACCAGCCTGGCCAA | 6709 |
rs535774917 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600009 | GAAACTAGAGTCATT[A/C]GCTGGAAAGGCCAGG | 6709 |
rs535892685 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582903 | GTAAGCTAAACACAG[C/T]TCTCACAAATAAATT | 6709 |
rs535902014 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633557 | CAGCTGCCCTCATTC[C/G]GACTTCAGAAAATCG | 6709 |
rs535930696 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554769 | AGGACTGCATAGCTC[A/G]TCACTGGGGGCCACT | 6709 |
rs536031465 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128552743 | GAGCGGGGCCCCGGG[C/G]AGCCGACCCCCGGGT | 6709 |
rs536046545 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557965 | CCCGCCACCACGCCC[A/G]GCTAATTTTTTGTAT | 6709 |
rs536067607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607382 | AGGGTGAAAAGATCT[C/T]AATTATAAGCCTACT | 6709 |
rs536079066 | snp | A/G/T | 0.000208891 | 0.010218 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632089 | GGTGACTGAGCTGAG[A/G/T]GCCCCCGTCTGAGCA | 6709 |
rs536198298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603031 | GTTGAAAGCTAATTC[A/G]CTGCTTTATTTTTTC | 6709 |
rs536215257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563147 | ATAGGCCAGTGCAGT[A/G]GCTCATGCTTGTAAT | 6709 |
rs536232856 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589562 | ATTACAGGCATGAGC[C/T]GCCGTGCCCGGCCTT | 6709 |
rs536243836 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567330 | GAGTTGCGCTCATGT[C/T]GCCCAGGCTGGAGTG | 6709 |
rs536244564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596139 | GTGAGCCACCGCACC[C/T]GGCCCATAATGTTTT | 6709 |
rs536258519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603148 | TTAGAGCTCCTGGCT[A/G]TTAAACAGTCTCAGC | 6709 |
rs536263217 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571583 | AGAGCGAAATTCTGT[C/G]TGAAAAAAGTAAAAA | 6709 |
rs536380741 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595560 | CTTTTTTTTTTAATT[G/T]GGGTAAATTCACAAA | 6709 |
rs536386915 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602317 | TGCCTCCTGGGTTCA[A/G]GCAATTCTCCCACCT | 6709 |
rs536395557 | snp | C/T | 6.60338e-05 | 0.00574566 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128608924 | CCAGCTCATCGCTGC[C/T]GGCCATTATGCCAAG | 6709 |
rs536409153 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561361 | TGGCGACAGAGCAAG[A/G]CTCCATCTCAAAAAA | 6709 |
rs536429546 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623510 | GCCCAGGCTGGGGTG[C/T]AGTGGCATGATCTCG | 6709 |
rs536499425 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589969 | CAGGCTTTGTCTTCT[G/T]TAGGCTAAATAATGA | 6709 |
rs536532548 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614486 | TCCCGGCTACTTGGG[A/T]GGCTGAGGCAGGAGA | 6709 |
rs536550863 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568202 | ATTGATTACAGTAAC[C/G]TAAGAAGAGAATGAA | 6709 |
rs536562365 | snp | G/T | 1.64955e-05 | 0.00287184 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583984 | GGTAGTGTGAACTGG[G/T]GGCTGTGGTTGGGCA | 6709 |
rs536623480 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609537 | CCTTCTATTACTGTT[C/G]CCAAATGCTGAGCTT | 6709 |
rs536659221 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609549 | GTTCCCAAATGCTGA[G/T]CTTCCTGGGGGAAGT | 6709 |
rs536670955 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624749 | GATGGCATAATGTGA[C/T]GTCATGGCATGAACA | 6709 |
rs536677804 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563813 | CATGCCTGGATAATT[G/T]TTTTTTTAGAGCCAG | 6709 |
rs536691004 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579445 | TTTGGAAAGGATTTC[A/G]TCAGTGAGTGATACT | 6709 |
rs536700139 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591797 | GGGTCTCAGACCCCT[A/G]ACTGATGACTTATAT | 6709 |
rs536774145 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602661 | TTATTTTCGAGTCGG[A/C]GTCTTGCTCCGTTGC | 6709 |
rs536793039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617415 | CAGTGCATCCCCAAC[C/T]CTCCAGAATCCGGAC | 6709 |
rs536834252 | snp | G/T | 0.000181853 | 0.0095338 | missense | SPTAN1 | GRCh38.p7 | 9:128584390 | GTGGCTCGCTATGAG[G/T]CACTCAAGGAGCCCA | 6709 |
rs536837745 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597775 | CCTGCCTCAACCTCC[A/C/T]GAACAGCTGGGATTA | 6709 |
rs536873019 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616232 | AAACATTTTTTTTTC[G/T]GAGATGGAGTCTCGC | 6709 |
rs536942346 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628279 | CCTGTCCAGCCACCG[A/G]GCTCTGTTGGGCTCT | 6709 |
rs536968453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590625 | GGGAGGCTGAGGTGG[A/G]TGGATCATGTGGTCA | 6709 |
rs536976023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597091 | CTTGAACCCGGGAGG[C/T]GGAGGTTGCAGTGAG | 6709 |
rs537053201 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128633084 | AAATCAAACTCAGTA[C/T]GGACAGAAGTCCCGG | 6709 |
rs537059480 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600392 | TGTTGTTGGCAGGGT[C/G]CCACCAGTAAGAGGC | 6709 |
rs537072995 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563895 | CGCCCACCTCAGCCT[A/C]CCAAAGTGCTGGGAT | 6709 |
rs537086195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571713 | TAAGTGTGCAAGGTG[A/G]CCATTATTTCCCTAT | 6709 |
rs537123386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605720 | AAAACGGCCAGGCAC[A/G]GTGGCTCACGTCTAT | 6709 |
rs537140352 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629900 | CCAGGGTTTCTGTGG[C/G]GAGGCTGTCAGGTTC | 6709 |
rs537232075 | snp | A/C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570767 | TTTCAAGTGATTCTC[A/C/T]TGCCTCAGCCTCCCG | 6709 |
rs537333974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618625 | AGTAGCTGGGACTAC[A/G]GGCACCCGCCACCAA | 6709 |
rs537339173 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557532 | GAGCTATATATCCCA[C/T]AAATACCCCCCAATT | 6709 |
rs537382602 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631751 | AGAATCACTTGAACC[C/T]GGGAGGTTGCAGTGA | 6709 |
rs537431187 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593391 | ATATGCTTCTCTTAA[A/C]GTGCTCTGATTCTTG | 6709 |
rs537438113 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582066 | GACATAATACAACTT[C/T]ATGGAAAAATGATTT | 6709 |
rs537473264 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561146 | AGGCCGAGGCGGGCG[G/T]ACCACAAGGTCGAGA | 6709 |
rs537552739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567158 | GTGGAATCTTAGAGG[C/T]ATTAATTGTCTTTTC | 6709 |
rs537568307 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592791 | AGGTGAACTAACCCT[A/C]TAATTTTCCTGCTAT | 6709 |
rs537568513 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599139 | AAACTCCAAAAATTG[A/G]TTTCTTTTTTTTTGA | 6709 |
rs537595625 | snp | A/C/T | 4.9513e-05 | 0.00497538 | missense, synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128626525 | TTTGCGCGAGGCCCA[A/C/T]GACGCCTTCCGCTCC | 6709 |
rs537620068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581569 | GTAAGAGAAGTTTCA[A/G]TAGAATGTGGAATAG | 6709 |
rs537629785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573468 | TTCTACTTTTTTATT[C/T]TTCCCGAGATGGATT | 6709 |
rs537663540 | snp | A/G/T | 3.29768e-05 | 0.00406048 | missense | SPTAN1 | GRCh38.p7 | 9:128605411 | GCAGCCTGGGGAAAC[A/G/T]TGCAGATCAGCGCAA | 6709 |
rs537687332 | in-del | -/TTTTG | 0.00517822 | 0.0506191 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567277 | TCTTGGAATGAGGTT[-/TTTTG]TTTTGTTTTGTTTTG | 6709 |
rs537763253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587546 | GGCAGGTTGGCGAGG[C/T]AGTGGAGGATGGGAG | 6709 |
rs537775797 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571947 | CTGCAACCTCCTTCC[A/G]CCAGGCTCAAGTGGT | 6709 |
rs537815189 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560672 | GGTGTGAGCCACTGT[C/G]TCTGCCTCACTGTTT | 6709 |
rs537864584 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615160 | GAAGTGACAGGCTCA[C/G]TTTATTTATTCTGGA | 6709 |
rs537915089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613665 | GGGCTCTTGAGAGAT[C/T]TTTATTATGTAGGTT | 6709 |
rs537916469 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625628 | GCAGGAAAGGGGGCA[A/T]GTGTGACTGAGTCTC | 6709 |
rs537946397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627752 | GACCATGCAGGGCGC[A/G]TGGTCAGCCCCAGCC | 6709 |
rs537969066 | snp | C/T | 0.000183271 | 0.00957088 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583031 | TGCAAGGGAACTTGA[C/T]GTTCTCAGGTTCAAG | 6709 |
rs538053471 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620115 | CATCCTCACTGCCTT[C/G]TGGCCAAAGCAAGTC | 6709 |
rs538068744 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611953 | CTAAATGGATTATAG[A/G]AGACTTTAGGCTGAA | 6709 |
rs538085253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128633112 | CGGATCTGCTTGTAG[A/G]AGCAGCTCCGAGCCC | 6709 |
rs538095966 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587131 | CGTTCTGTCGCTAGG[C/G]CTGGAGTACAGTGAT | 6709 |
rs538147929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128553815 | CTGTTCGGGAAGAAC[A/G]GGAGAGAGGCCATAT | 6709 |
rs538156861 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580869 | TGTTCTGTCTGCCTC[A/G]GAGGCATTGGGGCTG | 6709 |
rs538173384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594906 | CGATCTCGGCTCACT[A/G]CAACTCCTCCTCCCA | 6709 |
rs538213819 | in-del | -/TGTT | 0.00358779 | 0.0422022 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577653 | TACCTATGTTCTCTC[-/TGTT]TGGAGACTGGCAACT | 6709 |
rs538280421 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628740 | CGGCCAGGGGAGAAA[C/T]AGACCCATCCAGCCG | 6709 |
rs538283243 | snp | C/T | 9.9226e-05 | 0.00704295 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568743 | GCTGTGTGGTTGCGT[C/T]TGAGGCTCACTTCAA | 6709 |
rs538402865 | snp | C/T | 3.29919e-05 | 0.00406138 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632626 | GGAGTTCAAATCTTG[C/T]CTGCGCTCCCTGGGC | 6709 |
rs538458062 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627242 | CAAGTGCTCTGAGCC[A/G]GCCTCATGTCTCCCA | 6709 |
rs538479900 | in-del | -/TACGTTGTTGAAATG | 0.0182019 | 0.0936463 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602965 | GTTTTTAGAAGTAGC[-/TACGTTGTTGAAATG]TACGTTGTTGAAATG | 6709 |
rs538486469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128555770 | AACCAAGGGACTAAA[C/T]ATATTATCCTAGATA | 6709 |
rs538594808 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608124 | CCTGCCTCTTGCCCT[C/T]TTTAGCTGTTCCATC | 6709 |
rs538614125 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564466 | GTGTGCACCCATAGT[C/G]ACAGCAAGTGGGAGG | 6709 |
rs538666272 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597161 | TGAGACTGAGTCTCA[G/T]TAGAGAAAAAAAAGA | 6709 |
rs538678256 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558105 | ACCGCGCCCAGCTGT[A/G]TATTAGAAATTTCTA | 6709 |
rs538752394 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563934 | TGAGCCATGGCGCCC[A/G]GCCTATTCAACCAAC | 6709 |
rs538803396 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562352 | GTGATCCACCTGCCT[C/T]GGCTTCCCAAAGTGC | 6709 |
rs538832027 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570482 | AGCTGGGATTACAGG[C/T]GCCCACCACCATGCC | 6709 |
rs538924531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584611 | TGTCAGGATGGGCAG[A/G]GTCGAATTTAAATTA | 6709 |
rs538937597 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569383 | TGATGTGTGGCACCT[A/G]TTGGTCAATGACCAT | 6709 |
rs538985892 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577628 | TCACCTACAAATGCA[A/C]ATCACTTCTTACCTA | 6709 |
rs539026038 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614741 | TCATGATCACACCAC[C/T]GCACTCTTGGATGAC | 6709 |
rs539026080 | snp | A/G | 0.000117073 | 0.00765001 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604434 | TGAGGGGTCAGCCCT[A/G]GGCTGGGAGAGGGAG | 6709 |
rs539062498 | snp | C/T | 3.29843e-05 | 0.00406092 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128611761 | AGAGCTGCATGCCAA[C/T]GCTGACCGGATCCGT | 6709 |
rs539079831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619240 | GGGCCCTGTCATTCA[C/T]CAGGCAGCGCTGTGG | 6709 |
rs539108471 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573379 | TACCACAAACTGTCT[G/T]TTCACAGAAGGTCCA | 6709 |
rs539111821 | snp | A/T | 0.000331364 | 0.0128675 | SPTAN1 | 9 | allele_origin=T(germline)/A(germline) | 9:128609678 | CTGGTAAGTTTTTAA[A/T]TTTTTTAAGAGTTGT | 6709 |
rs539122936 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579048 | AAAACTTTGTTAAAA[A/G]GCATTAAATAAAAAC | 6709 |
rs539173896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623538 | TCGGCTCACTGCAGC[C/T]TCCACCTCCCAGGTT | 6709 |
rs539174609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610573 | TGTTTTTTTTTTGCC[C/T]CCCAAATAACACTCC | 6709 |
rs539211594 | in-del | -/TG | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625028 | AAAAAATGGTTTGTC[-/TG]GGTTTTGATGTTTTT | 6709 |
rs539248965 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592738 | TTTTCAGCACAGGAA[A/T]ATCTGCCTTAAGCAT | 6709 |
rs539262247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570989 | AAAGCAACATTAACA[A/G]TACTGTTAACTGGCC | 6709 |
rs539363143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585095 | TCTCAGCTCAGTGGA[A/G]CCTCTGCTTCCCTAG | 6709 |
rs539373936 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618684 | GAGACGGGGTTTCAC[C/T]GTCTTAGCCAGGATG | 6709 |
rs539387896 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600848 | TTGTATTTTTAGTAG[A/G]GACAGGGTTTCGCCA | 6709 |
rs539397575 | snp | G/T | 6.06594e-05 | 0.00550691 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593082 | AGCACCAATGTCCAC[G/T]GCTACCCTATCCATT | 6709 |
rs539407438 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564229 | TTCGAGACCAGCCTG[A/G]CCAACATGGTGAAAC | 6709 |
rs539521282 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599928 | CTTGTAGTTTGTTAC[A/C]AGCCAAACTATGGAG | 6709 |
rs539543374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631476 | AAAAAATTACTTGGG[C/T]ATGGTGGCCTACACC | 6709 |
rs539544825 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime | SPTAN1 | GRCh38.p7 | 9:128552626 | GGTGTGGAGCGGAGG[C/T]CGCGGAGGCTCCTCG | 6709 |
rs539584638 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594115 | TGGTTTGCCTTTATG[G/T]TAGCATCTACAGCTA | 6709 |
rs539608348 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630075 | TGGCCTTGGGAGCAA[C/G]ACGAGTGGGCTCAGC | 6709 |
rs539667519 | snp | C/G | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554041 | TCCCTTTCATTGCAG[C/G]TAACTAATGTCTTAG | 6709 |
rs539670231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630589 | GGCTGGAGTGCAGTG[A/G]TGCGATATTGGCTCA | 6709 |
rs539704545 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627266 | TCTCCCAGCCTCCTC[C/T]TCTCATCTTTGGGGA | 6709 |
rs539724071 | snp | A/G | 4.957e-05 | 0.00497821 | missense | SPTAN1 | GRCh38.p7 | 9:128605459 | CCCACGACCTGCAGC[A/G]CTTCCTTAGCGATTT | 6709 |
rs539769508 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593728 | GGATATTTTAAAGCT[C/G]AGTGTACCCTCCCCC | 6709 |
rs539784925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605764 | TGGTAGGCCAAGGCG[A/G]GCAGATCACCTGAGG | 6709 |
rs539891996 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593526 | AGATAATATTTCAGC[A/C]TTTTGTATTTTAGTT | 6709 |
rs539925228 | in-del | -/AGCT | 0.00438332 | 0.0466095 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617123 | CACACCTGTGGTCCC[-/AGCT]AGCTACTCCGGAGGC | 6709 |
rs539932966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600278 | AACTCTAAAATGTGA[C/T]GCTTAATATACAAAA | 6709 |
rs539948774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128553180 | CGGCCAGCCGTAGAG[A/G]GAGGAAGAGCCCGGG | 6709 |
rs539984997 | snp | C/T | | | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128550957 | TCTGGGGTGTGGTCA[C/T]TGCTTTTCTCTCCAC | 6709 |
rs539985611 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582980 | TGTAAGCCAACTGTT[C/T]TATACATTCCTCCAT | 6709 |
rs539987635 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619852 | CATTTCTTACTTCCA[A/G]TGGATCTGTGGATCA | 6709 |
rs539998293 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594587 | AGATGTGCGTCACCA[C/T]GCCCTGCTAATTTTT | 6709 |
rs540146141 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565957 | ATGGAGAGGGAAGGT[G/T]GCTAGTGTGAGGTCA | 6709 |
rs540207495 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128552290 | CAGGGCGTAGGCAGT[A/G]ACCTCACTGCACCAT | 6709 |
rs540238625 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602048 | TTTCAGAAATTTATT[G/T]TAGGTACCTTTATAA | 6709 |
rs540268290 | snp | C/T | 0.00186529 | 0.0304822 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632744 | TAAGGCCAGGTGCTG[C/T]GAGCCTCTGCCCGGG | 6709 |
rs540312297 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607186 | TTTTTCTTTTTTTTT[A/T]AGAGACAGGGTTGCA | 6709 |
rs540329107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568393 | TTTCAAGAGTAAGCA[C/T]TGAATGTTGAGAAAA | 6709 |
rs540410478 | in-del | -/CTGCT | 0.000131884 | 0.00811939 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617954 | CACCAGAAGAGCTAC[-/CTGCT]CTGCTGTTAACCTCC | 6709 |
rs540428033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599550 | TCTTGCTTTGTTGCC[C/T]AGACTGGAGGTCAGT | 6709 |
rs540428981 | snp | C/G | 1.84578e-05 | 0.00303786 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621278 | CCAGCCCATTGGTAA[C/G]ACCTCCATCGCCCAC | 6709 |
rs540467515 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128552376 | CGCTCACCTCTTCCC[A/C]CGCATTGTCGCTTCG | 6709 |
rs540515499 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613122 | GTTTCCTTGAACTAG[G/T]ATTGCTGTGCATTTT | 6709 |
rs540565147 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587321 | AACTCCTGGGCTCAA[A/G]CTGTCTGCCTGCCTC | 6709 |
rs540590446 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605948 | AGTGAGCCAAGATCG[C/T]GCCACTGCACTCCAG | 6709 |
rs540616975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561987 | GGGAGAACACAATAA[C/T]TTCATGGCAGAATGT | 6709 |
rs540628075 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616492 | ACGTTTGTGGCCGGG[C/T]GCAGTGGCTCACGCC | 6709 |
rs540705561 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615184 | TTCTGGACCGAGTAT[C/G]TGTGAGATACCAAGT | 6709 |
rs540745425 | snp | A/T | 0.000399281 | 0.0141238 | missense | SPTAN1 | GRCh38.p7 | 9:128568842 | CCATTGTTAAGCTGG[A/T]TGAAACTGGAAACCT | 6709 |
rs540752828 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561466 | CAAGAGATCGAGACC[A/G]TCCTGGCTAATATGG | 6709 |
rs540764031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622625 | TGCTTTGTCCTCAGC[A/G]ACAGCCTGTTTCCTC | 6709 |
rs540797387 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633662 | GATGACTTCCCCCAA[A/G]GCTTTGCTTTTCTTC | 6709 |
rs540849072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578026 | TTAGACATTTGAGAA[C/T]ATAGAATTCAGAGCT | 6709 |
rs540858728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628392 | TAAGTCCACAGCTGA[A/G]AAGGGCTGGGCACTG | 6709 |
rs540885853 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611168 | ATAGCTAGCATAGCT[A/C]CTGCAAGAATTGATT | 6709 |
rs540922784 | snp | A/C/G | 0.000422671 | 0.0145321 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627372 | CACAGCATCTGCCCC[A/C/G]CTTTGGCCCTCAGGA | 6709 |
rs540957603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574459 | GAGTAGATCTACCTA[C/T]TTGTAACTTGAAGAC | 6709 |
rs540978337 | snp | A/C | 0.0391387 | 0.134304 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623179 | TCCCACCTGAGCTTC[A/C]CTAGCTAGCTGGGAC | 6709 |
rs541002273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628306 | CTCTCACCTCTGCTT[C/T]CCCAGCGAGTCCAAC | 6709 |
rs541027484 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584658 | GTGGTAGCTAAGAAT[A/G]ACAAATCAGTGCTGA | 6709 |
rs541041474 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616980 | TGGTGGCTCACGCCT[A/G]TAATCCCAACACTTT | 6709 |
rs541049143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608598 | TGACAGCATTTTCCT[A/G]TTATCAGGCTTAATT | 6709 |
rs541058868 | in-del | -/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597003 | CATCTCTGCTGAAAA[-/T]ACAAAAATTAGCTGG | 6709 |
rs541081920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584095 | ATTTTCTTAGATCGC[C/T]CTGTGCTGCATGTGC | 6709 |
rs541114531 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595450 | AATTGAAACCTTTTT[A/G]GACAAATTTAGTTTT | 6709 |
rs541168430 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561911 | CTGAGTTCTGTGCCC[A/G]GAGAGTAAGAGTAAA | 6709 |
rs541218799 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583512 | AGAAGGAACTGAATT[A/G]GGCCTCATTGCTGAA | 6709 |
rs541238258 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615068 | GGCTCCTGGTGGTGG[A/G]TGTAAGTTTTCTAAA | 6709 |
rs541270442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596820 | CTCAGCCACCCGAGT[A/G]GCTGGGACTATGCAC | 6709 |
rs541275925 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557689 | CAAAGATATTCATGT[C/T]TAATCTATTTTGTAG | 6709 |
rs541407778 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629558 | CCAAGGCCACACGCA[C/T]CGTGTGATTCGTCCC | 6709 |
rs541428783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598862 | TTTCCATTTGTCCTT[C/T]TGGAATTATCTCCTG | 6709 |
rs541469452 | snp | A/G | 0.000230217 | 0.0107264 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630131 | TCCCATCTCTAAAAC[A/G]GGAGAAATGCTCCCT | 6709 |
rs541482514 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597381 | ATAAAATTATTTGCT[G/T]GGCATAGTGGTGTGT | 6709 |
rs541540141 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588154 | TGGCGCCCGCCACCA[C/T]GCCCAGCTAATTTTT | 6709 |
rs541564632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598092 | TAGCTGGGATTACAG[A/G]CATGGACCCCCACAC | 6709 |
rs541570752 | snp | A/G | 0.00132556 | 0.0257103 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605482 | AGCGATTTCCGGTAC[A/G]GAGCCATGTTCACTC | 6709 |
rs541580366 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559327 | AAATCAGCAAGCTGG[A/G]CCCAAGCAGGGGGAC | 6709 |
rs541584952 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575856 | CCACGTGTACAATCC[C/T]GTAAGCTGCTTCCAC | 6709 |
rs541629946 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562634 | TCAGGGTCCTCATCA[C/G]AAATCAGCCTTCTCC | 6709 |
rs541652702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603820 | GTGGAGCAAGCCTTC[C/T]CTCTGATTTCCAGTA | 6709 |
rs541671129 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596120 | AAGTGCTGGGATTAC[A/C]GGTGTGAGCCACCGC | 6709 |
rs541676041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578516 | GCTACTACTTGGCAC[A/G]TTGATCCTTTGTGAT | 6709 |
rs541689566 | in-del | -/G | 0.00206237 | 0.0320458 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617794 | GGCCAAGAGGGCAGA[-/G]GTGTTTGAGTGGGCC | 6709 |
rs541729297 | snp | C/T | 8.23839e-05 | 0.00641757 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609077 | CCACTTCCTTCTCCA[C/T]GGTAAGATATGCTCA | 6709 |
rs541896960 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128551281 | GCCCAGCTGTCACCG[G/T]AATGGGGATAGGGAA | 6709 |
rs541918337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619712 | TTTCCACATTCATGG[A/G]TACCAGAAGTTAGGA | 6709 |
rs541948030 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558536 | GCATTCCTAGGAAGT[C/T]GTCTCTGTTGTGGTT | 6709 |
rs541960678 | in-del | -/TTTTTTTTTTT | 0.405429 | 0.195811 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570331 | ATATATATATATATA[-/TTTTTTTTTTT]TTTTTTTTTTTTTGA | 6709 |
rs541970022 | snp | A/G | 0.000118278 | 0.00768929 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618135 | GAGGCAGGAGCTCCC[A/G]GGAACAAGTGGAAGG | 6709 |
rs541971435 | in-del | -/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578835 | TCACTCTGTCTCAAA[-/G]AAAAAAAAAAAAAAA | 6709 |
rs541986331 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571982 | CCACCTCAGCCTCCC[A/G]AGTAGCCGGCACCAC | 6709 |
rs541991860 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625247 | ATGACTGGTGGCGTC[A/T]TTCACTGAGGCATTT | 6709 |
rs542028439 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631552 | AAAATAAGGCTGGGT[G/T]CAGTGGCTCATGCCT | 6709 |
rs542031370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611246 | AGGCCAATGTGGCTC[A/G]ATTGCTTGAGCTCGG | 6709 |
rs542050918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587272 | GTATTTTCTGTAGAG[A/G]TGAGGTTTCAGTATG | 6709 |
rs542116995 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632976 | GGCCTCAGGAGGTGG[A/G]TGAAGAGGTGTCCTT | 6709 |
rs542144327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624542 | GCTGCTCTTTGTCTC[C/T]TTCCGTGTCATTGGT | 6709 |
rs542162290 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583364 | TTTTAGGGACATATA[C/T]CCCCCAAGAAAGGTG | 6709 |
rs542168540 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613228 | GCCGGGCAGGCTGAT[G/T]GGGGTGGCTAGGAAT | 6709 |
rs542188247 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593617 | ATACTCAGTACTGTG[C/T]CTGATTTTCCTTCTG | 6709 |
rs542200221 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612911 | GCCTGGGCAACAGAG[C/T]GAGACTTCATCTCAA | 6709 |
rs542214677 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568627 | TTGAGGAATTGAGCA[A/G]GTAAGAGAATGGGCA | 6709 |
rs542248962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560176 | GCAACCTCAGCCTCC[C/T]GGGTTCTGGCAATTC | 6709 |
rs542260546 | snp | C/G | | | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128551643 | ATGAAAAGGTAACAC[C/G]AAATACTTAGCATAG | 6709 |
rs542266768 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606082 | TATTGTTAAAAATAA[G/T]TCTCTGCAGCCGGGC | 6709 |
rs542269412 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572022 | CAAGCACACTGAGCT[A/G]TTTTTTTTGTATTTT | 6709 |
rs542356556 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573649 | TTTAGTAGAGACGGG[G/T]TTCACCATGTTGGCC | 6709 |
rs542361260 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615969 | GCTTGGGCACACAGT[C/T]GTGGGATGCCTCAGT | 6709 |
rs542384324 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588966 | ACAGAGAGTGGCTGT[C/G]TGTTTGTTCCACGCT | 6709 |
rs542394532 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619172 | GATCTCACACTAGGG[A/G]ACATCACCCTTCAGT | 6709 |
rs542558608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560911 | ATCCCAGCTACTGGG[A/G]AGGCTGAGGCAGGAG | 6709 |
rs542757208 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128555236 | ACTGAAAAAATATCT[A/G]AAATTGGATTTTTAA | 6709 |
rs542762132 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602653 | TTATTTATTTATTTT[C/T]GAGTCGGAGTCTTGC | 6709 |
rs542784568 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632398 | CACCTGCTGTGTGGA[A/G]GGTCTGTTCCCTAAT | 6709 |
rs542788794 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568974 | CATACATGTCAGTTT[G/T]GGTTCCCAAAAAGAT | 6709 |
rs542845652 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601046 | TGGAGTGCAGTGGCA[C/T]GATCTCAGCTCACTG | 6709 |
rs542848685 | snp | C/T | 0.00013392 | 0.00818182 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632329 | TCCAGGCCAGGTACC[C/T]GGGAGGGCTGTGGGC | 6709 |
rs542868662 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575111 | AGCTAACATGGCTCC[A/G]TCCCTAATGTGTCTG | 6709 |
rs542875829 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607781 | ATTCCCACCCTTTGT[C/G]GTGAGTCGGTGGTTG | 6709 |
rs542891929 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561998 | ATAATTTCATGGCAG[A/T]ATGTGGCAGTGTTAT | 6709 |
rs542966508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617551 | GAAAGATTAGTAGAT[A/G]TCTGTGAGGTCCACA | 6709 |
rs543063864 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603346 | ATTACTCAGTTGAGT[C/G]TAATTGTGCACTTTG | 6709 |
rs543092105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557172 | CATCCTGTTAGTCCC[C/T]AAAAATCCCTTTCTT | 6709 |
rs543177130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622745 | TAGTATGGTTTATTT[A/G]TTTATTTATTTATTT | 6709 |
rs543227930 | snp | A/C | 0.00052911 | 0.0162565 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632121 | CTGTGCTCCCCACCC[A/C]TGCAGCGCAAGCACC | 6709 |
rs543315120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590350 | GTAACTACTAGCTAC[A/G]TGTGATAGTAAGCCC | 6709 |
rs543419438 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630827 | CTCCTGCCTCAACCT[C/G]CCAAGTAGCTGGGAT | 6709 |
rs543494879 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577769 | GGAATGTCCCTTTAA[C/G]TATCTGAGTATCACA | 6709 |
rs543556144 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578404 | GCCTTTGGAGACCTG[G/T]TCTACCTGCTTCTGA | 6709 |
rs543560351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570648 | CAGCCCAGATGGCTT[A/G]TTTATTTATTTATTT | 6709 |
rs543569770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628879 | TGTCTGCTGGTCTTG[C/T]TCTTGTCTCCGTGAG | 6709 |
rs543615028 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626333 | CACCCCACCTCCTGC[A/G]CTGCGTCGGCACGTC | 6709 |
rs543619314 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624959 | GTGCAGGGAGGGGCC[C/T]GCTAATGTGGGTTCT | 6709 |
rs543631449 | snp | G/T | 1.64814e-05 | 0.00287061 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576977 | AAGCCAGAGTGGGCT[G/T]TGGGGAATGGGTCTC | 6709 |
rs543727650 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590882 | AACTCAATGAAAGTT[A/C]AGTGGGCACATGTGA | 6709 |
rs543779093 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588550 | CCCCGACCTCAGGTG[A/G]TCTGCCTGCCTCAGC | 6709 |
rs543790625 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579319 | GGTTCTATAAAATCA[G/T]AGTAAACAAGTCCAT | 6709 |
rs543817788 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593748 | TACCCTCCCCCACCT[A/C]ACCCCAGCCTGGGGG | 6709 |
rs543863459 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618227 | GACCTTTGGCCTCAC[A/G]TGTGCCATAGTCGGT | 6709 |
rs543922756 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586287 | CTACCTGCCTAGCTA[C/T]GCTTTTTAATTTTAA | 6709 |
rs543947812 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605915 | GAGAATCGCTTGAAC[C/G]TGGGAGGCGGAGGTT | 6709 |
rs543982760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565633 | CCTTCTGTTTACCTG[C/T]TAGGTGGATGTGGGG | 6709 |
rs544004598 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564914 | TACTTCTATCCGCCA[C/T]AAGGGTAGGGGTCAC | 6709 |
rs544030213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597978 | TTTGAGATGGAGTTT[C/T]GCTCTTGTTGCACAG | 6709 |
rs544042080 | snp | C/G/T | 4.94192e-05 | 0.00497067 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128591563 | CGCCCAGTCAGCCTC[C/G/T]CGGGAGAATCTCCTG | 6709 |
rs544055404 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572086 | GCTGGTCTTGAACTC[C/T]GGAGCTCAAGCAATC | 6709 |
rs544070220 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628864 | CCTGCCCCATGCCTG[A/T]GTCTGCTGGTCTTGC | 6709 |
rs544100460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557805 | TAGAAATTTCTTTTT[C/T]TTTTTTTTTTTTTTT | 6709 |
rs544130260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580147 | GTGAGACCCCCATCT[A/G]GACAAAAAATTAATA | 6709 |
rs544152141 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614569 | TATTCCAGCCTGGGC[A/G]ACAGAATGAGACTAC | 6709 |
rs544234739 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631655 | ATGCAGTGAAACATC[A/G]CCTCTACTAAAAATA | 6709 |
rs544291305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613950 | GCGGAGGTTGCGGTA[A/G]GCCAAGATCGCGCCA | 6709 |
rs544342083 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570016 | AACCCATTTGGGCAA[C/T]GTAATATGTGTTTGC | 6709 |
rs544362052 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610479 | GCTGAATTGAGCCAG[A/G]TGGCTCCATCCTTTG | 6709 |
rs544375267 | snp | G/T | 3.29946e-05 | 0.00406155 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612076 | CGATTCTTCATAGAT[G/T]TCATCTCTTTTTGGC | 6709 |
rs544409892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605573 | GCTCAGCAGGGTACA[A/G]TGGCTCACACCTATA | 6709 |
rs544415266 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574572 | TTAAAAATATTTTTA[C/T]TCAGCGCTCCATAAG | 6709 |
rs544418154 | in-del | -/TAAA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604935 | GAAACTCCATCTCAG[-/TAAA]TAAATAAATAAATAA | 6709 |
rs544432822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620444 | ACCTGGGGCCAGGTG[C/T]GGTGGCTCACACCTG | 6709 |
rs544447518 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626777 | TAACTGAGTCACGAC[A/T]AGACGAGCAGGATGG | 6709 |
rs544475693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587360 | AAAGTGCTGGGATTA[C/T]AGGCATAAGCCTCTG | 6709 |
rs544477435 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594550 | GTTCTCCTGCCTCAG[C/G]ATCCTGAGTTGCTGG | 6709 |
rs544570655 | snp | A/T | 0.097727 | 0.198275 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606485 | GACATATATATATAT[A/T]TATTTTTTTTTTGGG | 6709 |
rs544617296 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576668 | TAGAAACTCTTTGGA[A/G]TTGTAGTTCACTTTG | 6709 |
rs544645672 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621991 | TTCCTGTCACACACA[A/C]ATCATGAGTAAGATT | 6709 |
rs544660849 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561422 | TAATCCCAGCTCTTT[C/T]GGAGGCCGAGGCAGG | 6709 |
rs544674143 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575984 | TAAATCTGCTTATAG[G/T]CTGGTACTTGTTTCC | 6709 |
rs544709386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574957 | GGTTGCTGTCTCTCC[A/G]GCTGCTCTCTAGGTG | 6709 |
rs544738830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567432 | AGGTTGCTGGGATTA[C/T]AGGCGCCTGCCACTG | 6709 |
rs544812511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583402 | TGACTTTGGCGTTAG[A/G]GATAATTTCCTGTGT | 6709 |
rs544843583 | snp | A/G | 0.000198304 | 0.00995555 | missense, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633290 | CGCGAGCTCCCCACC[A/G]CGTTCGACTACGTGG | 6709 |
rs544843840 | snp | C/T | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128553814 | GCTGTTCGGGAAGAA[C/T]AGGAGAGAGGCCATA | 6709 |
rs544894986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626273 | CAGAGGGGAGCTAAG[C/T]TCCCAGCAGGCTGTG | 6709 |
rs544926032 | snp | A/G | 6.60786e-05 | 0.0057476 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581091 | GCCTTGCCAGTGGTG[A/G]GAGAAGAAGGGCCTG | 6709 |
rs544952934 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628358 | AGATGGCAGTGCTGG[G/T]GGCTCAGGCAGGGTA | 6709 |
rs544960333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601181 | AGAGATAGGGTTTCC[C/T]TGTGTTAGCCAGGCT | 6709 |
rs544981004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554224 | ACCTTGATGGAGAGA[C/T]TGGAAAGGAGGATTT | 6709 |
rs544987394 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584062 | CTAAATGAATTTTGG[A/G]AGGGATGAAATGTGT | 6709 |
rs545019546 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622601 | ACCACCCCCGGCCAG[C/T]GAGCCGGCTGCTTTG | 6709 |
rs545050150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615578 | GAGTTCTTATGTTCA[A/G]GCAGATAGCTGTGGG | 6709 |
rs545097306 | snp | A/G | 1.69611e-05 | 0.00291209 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632983 | GGAGGTGGGTGAAGA[A/G]GTGTCCTTTGGAAAA | 6709 |
rs545169220 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601382 | CCAGCTCTTCAGGAA[C/T]ACATCACTTGAGTTA | 6709 |
rs545233119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595652 | ACCACCTCTAGTTCC[A/G]AAACATTTGTGTCAC | 6709 |
rs545235128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589012 | GCTCAGTTGGGTTTC[C/T]GTGGGTTGCATGTCT | 6709 |
rs545251518 | in-del | -/CTC | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590974 | TGGCAGGCGGCATTG[-/CTC]TTCTGCCTGTGACCC | 6709 |
rs545288699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602696 | GCTGGAGTGCAGTGG[C/T]GCAATCTCAGCTCAC | 6709 |
rs545349364 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611156 | CTTCACTCCCAAATA[A/G]CTAGCATAGCTACTG | 6709 |
rs545420772 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575452 | TTTCTGAGTGAGCAA[A/G]TTTTTGTAAGCATGT | 6709 |
rs545424690 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571986 | CTCAGCCTCCCGAGT[A/G]GCCGGCACCACAGGA | 6709 |
rs545437421 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604099 | CTGCTGCCTCAGAGA[C/G]GATGCCTAGGTCAGG | 6709 |
rs545470751 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618539 | CCCAGGCTGGAGTGC[A/G]GTGGCACAATCTCGG | 6709 |
rs545486328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610008 | AGCTTTTTCTGTGTA[A/G]ACATTGGCTCAGACT | 6709 |
rs545491424 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557067 | GGTTCTGACTAAGCA[A/G]CAAAAGCAACTGATG | 6709 |
rs545530374 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596781 | CTGTAACCTCAAACT[C/T]CTGTGCTCAAGTGAT | 6709 |
rs545545681 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587541 | AGGATGGCAGGTTGG[C/T]GAGGCAGTGGAGGAT | 6709 |
rs545593354 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606890 | ACGGTGTTGTGCAGC[C/T]ACCCCTCTCTAGTTT | 6709 |
rs545640892 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576677 | TTTGGAGTTGTAGTT[C/T]ACTTTGTATCATGTT | 6709 |
rs545666174 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591410 | TGTGTGTGTATACAC[A/G]TGACCTCCTTGGATT | 6709 |
rs545741634 | in-del | -/GCTGTA | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558836 | AGTTTCGGGTGAGAG[-/GCTGTA]GCACCTTTGGATGGC | 6709 |
rs545754581 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573713 | CCCACCTCAGCCTTC[C/T]AAAGTGCTGGGATTA | 6709 |
rs545775956 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623396 | TAAGTGATATGATTC[A/C]GTTTTTTTCTATCAA | 6709 |
rs545797428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564728 | GGAACATTGGGTACA[A/G]TTTAGTAAAGAGTCA | 6709 |
rs545799327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557852 | TCTGTCGCCCAGGCT[A/G]GAGTGCAGTGGCGCG | 6709 |
rs545810711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578002 | CAGAATTAGAATTTA[C/T]ATAGTTTGTTAGACA | 6709 |
rs545819659 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562166 | GGAGTGCAGTGACGC[A/G]ATCTGGGCTCATCAC | 6709 |
rs545860528 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558448 | ATTTCCCCTCCTTCA[G/T]TCTCTATGTGAACAG | 6709 |
rs545900385 | in-del | -/CAT | 0.00161338 | 0.0283564 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578082 | AACCTCCGCTGGAAA[-/CAT]AATGTCTTCCTTTGG | 6709 |
rs545948305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623857 | TTGGGAAGCCGAGGT[A/G]GGCAAATCACCTGAG | 6709 |
rs545948970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570496 | GCGCCCACCACCATG[C/T]CCGGCTAATTTTTGT | 6709 |
rs545977603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578470 | CTGTGGTCCATAAAA[A/G]CAAACAGACAAGCTC | 6709 |
rs546049999 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128551185 | CTTGGTAACCAGGAG[C/G]CTGAAGCCTTCCTAA | 6709 |
rs546089356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592924 | GAGCTGCTGCCTTTC[A/G]TCCCTGTGGATTAAC | 6709 |
rs546120713 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595817 | ATGTCACTTTTTGTG[A/C/G]CTGGCTTCTTTTGTT | 6709 |
rs546138632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618781 | AGCCACCATGCCCAG[C/T]TTTTGTGACTGTTTT | 6709 |
rs546177701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573024 | TGTTGACTGTCACAT[A/G]GTTTTCAGGTTTTCA | 6709 |
rs546192604 | snp | C/G/T | 8.38075e-05 | 0.00647277 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575386 | CTCACAACATTATTA[C/G/T]GTTAACTTTTTAGTA | 6709 |
rs546203862 | in-del | -/TTAT | 0.00597247 | 0.0543191 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570645 | CCCAGCCCAGATGGC[-/TTAT]TTATTTATTTATTTA | 6709 |
rs546225589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598727 | GGCTTCTGTCTTCTC[C/T]GTAAGCTCATTAAAT | 6709 |
rs546239559 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612321 | GGTCCATCAGTGCCC[A/C]AAACCACGAAAAGGC | 6709 |
rs546248042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626322 | GAACCACCCCGCACC[C/T]CACCTCCTGCACTGC | 6709 |
rs546275119 | snp | G/T | 1.68303e-05 | 0.00290084 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625221 | AAATGTATGCAGATA[G/T]CATCTGTGAGATGAC | 6709 |
rs546289940 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610771 | CCCTTTCATTTCCCA[A/G]TAAAATAAATTCCTT | 6709 |
rs546304880 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578802 | CCATTCCACTCCCGT[C/T]CGGACAACAAGAGTG | 6709 |
rs546316885 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580649 | TTTTAAATGGATGCC[C/T]TATTTCTTCTACCTG | 6709 |
rs546334998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587459 | AAAACTTTGAAAATG[A/G]TATTAGCACTGTAAG | 6709 |
rs546389394 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575844 | CTTCCCCAGTGCCCA[C/T]GTGTACAATCCTGTA | 6709 |
rs546449592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558685 | GGGAACAGCCTGGAA[C/T]GTTCTCTGTGAAGTC | 6709 |
rs546557618 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603723 | TATTGGGTCCAAGCA[C/T]GTCCTAAGTAAACAT | 6709 |
rs546565541 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573385 | AAACTGTCTTTTCAC[A/G]GAAGGTCCAAAGTTT | 6709 |
rs546598575 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563200 | GCATGTGTATCACTT[A/G]AGTCCAGGAGTTCGA | 6709 |
rs546637639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627117 | TGTACCCAGCCAGAA[A/G]TTTCCATTTCTGACA | 6709 |
rs546750051 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557835 | TTGAGACGGAGTCTC[A/G]CTCTGTCGCCCAGGC | 6709 |
rs546757260 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600530 | TTCAGAGATGCCCAA[A/T]ACAGAGATGTAAAGG | 6709 |
rs546860426 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631200 | TGGTGACTTACACCT[G/T]TAATCCCAGCACTTT | 6709 |
rs546895909 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128550706 | TTTGCTGGAGCAGAA[A/G]GTCTTGGAAATTTTA | 6709 |
rs546949505 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573745 | AGGAGTGAGCCACTG[C/T]GCCCAGCCCTTTTCT | 6709 |
rs546979258 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595278 | CCACATCTGGCAAAT[G/T]TTTGTATTTTTAGTA | 6709 |
rs547012864 | snp | C/T | 6.60666e-05 | 0.00574708 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128566866 | TCAGAAGCTGGAAGA[C/T]TCCTATCGATTCCAG | 6709 |
rs547022499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588531 | GGTCAGGCTGGTCTC[A/G]AACCCCCGACCTCAG | 6709 |
rs547027952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128555536 | ATGACGTTTCTGTTA[A/G]ACAAATTGGTTAGGA | 6709 |
rs547078927 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | SPTAN1 | GRCh38.p7 | 9:128552638 | AGGCCGCGGAGGCTC[C/T]TCGGTCCTTCAGCAC | 6709 |
rs547129870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614032 | AAATGCTGAATTCAG[A/G]TTGTGGTGTTTTGCA | 6709 |
rs547131014 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568614 | GCAGTCAGAGTATTT[C/G]AGGAATTGAGCAGGT | 6709 |
rs547188736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599934 | GTTTGTTACCAGCCA[A/G]ACTATGGAGGGAAAA | 6709 |
rs547200980 | in-del | -/ACTA | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559001 | AGGGGGGAAACTCTC[-/ACTA]ACCCATAATGTTTTT | 6709 |
rs547250238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621646 | TGTCTGACCTGCCAG[A/G]CCTTTCTTTTCTCTC | 6709 |
rs547264696 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575480 | TGTCTGAGAGTTTTG[C/T]TTAGATGTGAGGCAC | 6709 |
rs547286889 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623149 | TAGCCTCTGCCTCCC[A/G]GGTTTCAGCAGTTCT | 6709 |
rs547293141 | snp | C/G | 0.00316956 | 0.0396829 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627202 | CCTTGAAGCCCCTGG[C/G]GGGTGGGAACAGAGA | 6709 |
rs547300818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627672 | GGAGTGGGGGCATAG[A/G]TGGAGCAGCCTCTCA | 6709 |
rs547343059 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557364 | CTCTCTTTTGGGATT[C/T]CATAGAGAAACTGAC | 6709 |
rs547401060 | in-del | -/C | 0.0607341 | 0.163335 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626817 | TTTCATCAGAAGTTT[-/C]CATTTCTTTTTGTGT | 6709 |
rs547444256 | in-del | -/AGAC | 1.72228e-05 | 0.00293447 | downstream-variant-500B, intron-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128633993 | GTCACCTGCAAAGAG[-/AGAC]AGATACGTGGAGTAA | 6709 |
rs547447240 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616706 | AGGGAGGCGGAGGTT[G/T]CAATGAGCCAAGATC | 6709 |
rs547467703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576073 | TTCCACAGTGACAGA[C/T]GTGTTGCTTTTCCAA | 6709 |
rs547483474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569145 | AATGTGATTATACTT[C/T]AAAGAAAACTGTGAA | 6709 |
rs547512661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607360 | TAGCTAGAACTTGTT[A/G]TTCTGGAGGGTGAAA | 6709 |
rs547516794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584933 | GTGGGCATCACAAAC[C/T]AGGCTCTGGGGCTGA | 6709 |
rs547594503 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614436 | GTTTCTACTGAAATA[C/G]AAAAAATTAGCAGGG | 6709 |
rs547636172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589246 | CCAAAGTTTGCTTTC[C/T]GTATAACTTGGACCT | 6709 |
rs547682941 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582134 | CCTTCATTAAAAGTA[C/G]GTCAGGGTTAATATT | 6709 |
rs547751442 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596088 | AGCTCAGGCCGTCTG[C/T]CCAGCTTGCCCTCCC | 6709 |
rs547771502 | snp | A/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128585916 | GGATGCGGGAGAAGG[A/G]ACCCATTGTGGGCAG | 6709 |
rs547822778 | snp | C/T | 1.65154e-05 | 0.00287358 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630427 | TTCACCCAGCCACCC[C/T]CCAGGGTACCCCTTC | 6709 |
rs547858679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597744 | ACCTCTGCCGCACCC[C/T]GGTTCAAGCGATTCT | 6709 |
rs547879640 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592602 | TACCAGTAGTCTGGG[C/T]CATAAATATAAGAGG | 6709 |
rs547919901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629004 | TGCCTCCAGGTACCC[A/G]CCGGGCACCAGGTTG | 6709 |
rs547921727 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622909 | AGGCGCCTGCCACCA[C/T]GCCCAGCTAATTTTT | 6709 |
rs547974297 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590548 | ATCTCTATTTATATT[A/T]AAAAAGAAAAAAAAA | 6709 |
rs547995280 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597053 | TAGACCCAGCTACTC[A/G]GTACACTGAGGCATG | 6709 |
rs548005480 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604197 | CTAATTTATTCAGCG[A/G]GGAAGGTTGGAAACA | 6709 |
rs548039378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610279 | TCAAAGTTACTTAAG[C/T]GGGTGGAAGAAATGA | 6709 |
rs548056671 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628520 | ATGTGATAGACAGGA[C/T]GTGGGAGGAGCCCCA | 6709 |
rs548094775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602842 | GGTTTCACCATGTTG[A/G]TCAGGCTGGTCTCAA | 6709 |
rs548108686 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622488 | ATTGTTAGTAGAGAT[A/G]GGGTTTCTCCATGTT | 6709 |
rs548109418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596477 | GAGATGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 6709 |
rs548197086 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559612 | GAAGCAAACAAATTA[-/G]ATGCATAATTTCTCA | 6709 |
rs548217261 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128551856 | GAAATTAACTCTCCA[A/T]ATCCCAGAATGACAG | 6709 |
rs548278706 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590067 | GAAGCATGCACAGAT[G/T]GACTGATCCTGAAAG | 6709 |
rs548383055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557485 | AACGCAGTGGGATTC[C/T]CACCCACTGCCTCTG | 6709 |
rs548394247 | in-del | -/A | 0.480823 | 0.0960254 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571294 | ACTGGGAAAAAGAAA[-/A]AAAAAAAAGGCCAGG | 6709 |
rs548416338 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570907 | CTCAGGTGATCTGCC[C/T]GCCTTGGCCTCCCAA | 6709 |
rs548434026 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621812 | TTTTGGGAGAAAAAA[G/T]AAAGGGGCTTGGTGC | 6709 |
rs548442578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557890 | CTCACTGCAAGCTCC[A/G]CCTCCCAGGTTCACG | 6709 |
rs548477218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563782 | GTACAGTAGTGTGAC[C/T]ACGGGCGCATGCCAC | 6709 |
rs548562094 | snp | A/G/T | 0.00319098 | 0.0398384 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574578 | ATATTTTTATTCAGC[A/G/T]CTCCATAAGGTCTCT | 6709 |
rs548564730 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605717 | TCAAAAACGGCCAGG[C/T]ACAGTGGCTCACGTC | 6709 |
rs548564853 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586432 | ACCACCCCTTCTGGC[C/G]CATTTTTCACTTTTT | 6709 |
rs548597771 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615923 | GACTGTTGAGTGGTG[A/T]GGCTGGAAACCCTGC | 6709 |
rs548615710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599118 | TTGTGTGTAAAGATT[C/T]GTGGAAAACTCCAAA | 6709 |
rs548632596 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581441 | TCGTACCACCGCACT[A/C]TAGCCTGTGCAACAG | 6709 |
rs548689317 | snp | C/G | 0.000131983 | 0.00812243 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605221 | CTGGCATTTTTGCCC[C/G]AGAAAGAGCAGAGTC | 6709 |
rs548715919 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561008 | GCAACAGAGCAAGAC[C/G]CCATCTCAAAAAAAA | 6709 |
rs548728129 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614106 | GGAGGAATATTTTGA[G/T]TCGGGTAAGTGTGAA | 6709 |
rs548864403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578754 | GAATCGCTTGAACCC[A/G]GGAGGCAGAGGTTGC | 6709 |
rs548868118 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128552423 | CTCGGCCCTTTCCGC[C/T]GGGCGGTCGGGCGGC | 6709 |
rs548928580 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613586 | GAGAGTGACTTCTTT[C/T]ACTTAAAGCAGCCAT | 6709 |
rs548941964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627747 | AGTGGGACCATGCAG[A/G]GCGCGTGGTCAGCCC | 6709 |
rs548964301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620887 | TTGATGGATGACAAA[A/G]GGTTTGACCCTTCCC | 6709 |
rs549003751 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621752 | ATCAAAAACCTCGAG[C/G]CTGTACAGGGCATTT | 6709 |
rs549045614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593938 | CTGGGGATAAGTGTG[C/T]CTGGCTGTTCTAGCC | 6709 |
rs549061995 | snp | A/G | 0.00104345 | 0.0228174 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592979 | CTGTGCCCCCTCTGT[A/G]CAGGACACGCATAAC | 6709 |
rs549100883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619984 | TGTCATCCAGCCTGG[A/G]CATCTCTGTTCCCCT | 6709 |
rs549128114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600732 | CAGTGGCACAATCTC[A/G]GCTCACTGCAACCTC | 6709 |
rs549189455 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594897 | GCAATGGTGCGATCT[C/T]GGCTCACTGCAACTC | 6709 |
rs549230068 | snp | C/G | | | downstream-variant-500B, missense | SPTAN1, WDR34 | GRCh38.p7 | 9:128633822 | GAACTCTGTGCTCAG[C/G]TGCCACACCTTCACT | 6709 |
rs549235701 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593275 | CTGTGTGTTCAGAGT[A/G]GTGTTGGTTCTCCCT | 6709 |
rs549237171 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623766 | GGCGTTAGCCACTGC[A/G]CCTGGCCCATATTTC | 6709 |
rs549268133 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567631 | TAGTGATGTTGCTGG[C/G]AAAAATTTATAGTTA | 6709 |
rs549278392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631284 | CCAACATGGGGAAAC[C/T]CCATCTCTACTAAAA | 6709 |
rs549360347 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589810 | TCGATCTCCTGACCT[C/T]GTGATCCACCCGCCT | 6709 |
rs549394239 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562765 | GTCAGGAGATCGAGA[C/T]CATCCTGGCTAGCAC | 6709 |
rs549464710 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592136 | CACTTGGGAAATATC[C/T]AGGAAATACATTCCC | 6709 |
rs549528366 | snp | C/T | 0.000313265 | 0.0125114 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128615823 | CCGGGACATGGATGA[C/T]GAGGAGTCCTGGATC | 6709 |
rs549534037 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561524 | AAAAATTAGCCGGGC[A/G]AGGTGGTGGATGCTT | 6709 |
rs549567531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562264 | CGTGCCACCACACCC[A/G]GCTAATTTTTGTATT | 6709 |
rs549578399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128553796 | GAAAAACTTACCATC[A/G]TGGCTGTTCGGGAAG | 6709 |
rs549601680 | in-del | -/AAA | 0.00396038 | 0.0443227 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571292 | AAGACTGGGAAAAAG[-/AAA]AAAAAAAAGGCCAGG | 6709 |
rs549627187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128555736 | CTGACTTTTTATTGG[C/T]GGCTACTTGGTTTTT | 6709 |
rs549701686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602938 | AGCATGCCTAGCCCT[A/G]AGGGACTTTAGGTTT | 6709 |
rs549736000 | snp | C/T | 6.58935e-05 | 0.00573955 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608114 | CATTTTCTCACCTGC[C/T]TCTTGCCCTCTTTAG | 6709 |
rs549761259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563914 | AAGTGCTGGGATTGC[A/G]GATGTGAGCCATGGC | 6709 |
rs549761287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571486 | GCTAGTTGGGAGGCT[A/G]AAGCAGGAGAATTGC | 6709 |
rs549824811 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596522 | ACCTCGTGATCCACC[C/T]GCCTCGGTCTCCCAA | 6709 |
rs549855620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569954 | TAATGATGATTGTAA[A/G]TAGGAAATAAAAGTG | 6709 |
rs549874619 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609569 | CTGGGGGAAGTATGA[A/C]AAAATGAGTTTCTAT | 6709 |
rs549892132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602359 | GTAGCTAGGATTACA[A/G]GCACCCGCCACCATG | 6709 |
rs549896768 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570946 | GATTACAGGCATGAG[A/C]CGCCGCTCCTGGCCT | 6709 |
rs549979206 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585568 | GAGGAGGCAAAAAAT[C/G]AAACAGTCCATTAGA | 6709 |
rs549980014 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585216 | GTATTTTTAATAGAG[A/T]CAGGGTTTCACCATA | 6709 |
rs549999505 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620033 | TCAAGCTGGCTAGAC[C/T]AACCTCCTTCAGCAG | 6709 |
rs550041757 | in-del | -/TTTC | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630538 | ACTATCTCTCTCTCT[-/TTTC]TTTCTTTCTTCATGG | 6709 |
rs550128217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576179 | ACCCTGAAATGCTTC[A/G]TTTTATTACTTTGTA | 6709 |
rs550166982 | snp | C/T | 3.34096e-05 | 0.00408702 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617808 | AGGTGTTTGAGTGGG[C/T]CCCAGGGGACAGACA | 6709 |
rs550178651 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610414 | CCCTTTTCCTTCTTG[G/T]CTTTGGGATCAGGCG | 6709 |
rs550202632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618641 | GGCACCCGCCACCAA[A/G]CCCAGCTAATTTTTT | 6709 |
rs550221689 | snp | C/T | 4.9423e-05 | 0.00497082 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578097 | CATAATGTCTTCCTT[C/T]GGTTTTCCCTAGGCT | 6709 |
rs550254434 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623002 | ATGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 6709 |
rs550303572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624059 | CTGCATTCCAGCCTG[A/G]GCGACGGAGTGAAAT | 6709 |
rs550346968 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625455 | AAGGGGCAAGTTCTC[A/C]TAAGCGAAATCATGA | 6709 |
rs550359608 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585077 | TGGAGTGCAGTGGCG[C/T]GGTCTCAGCTCAGTG | 6709 |
rs550382864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598168 | GGTTAGGTTGGTCTC[A/G]AACTCCCGACCTCAG | 6709 |
rs550419366 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564361 | GATGCAGAGGTTTCA[A/T]TGAGCCAAGATCATG | 6709 |
rs550440285 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623497 | GTCTTGCTGTGTTGC[C/T]CAGGCTGGGGTGCAG | 6709 |
rs550474373 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557709 | CTATTTTGTAGGAAT[A/C]CATTTTCAGTTGATA | 6709 |
rs550477431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565079 | GGAGGCTGAGGCAGG[C/T]AGATCACGAGGTCAA | 6709 |
rs550535403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560122 | AGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 6709 |
rs550640554 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566584 | ATAAAGAAATAGGAT[C/G]TGGGCTTCATTGTTC | 6709 |
rs550700587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586470 | AAATGTAATCATACC[C/T]AAAGGAGAGAGAAGA | 6709 |
rs550715223 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559413 | TGTTCCCAAATGTGA[-/T]TTTAATTTCTGTAGC | 6709 |
rs550790163 | snp | C/T | 0.000247119 | 0.011113 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128613420 | GATTATGGCAAAGAC[C/T]TAGCTTCTGTGAACA | 6709 |
rs550815828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560303 | TGCCCAGGCTTGTCT[C/T]GAACTCCTGAGCTAA | 6709 |
rs550872320 | in-del | -/TATA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575468 | TTTTGTAAGCATGTC[-/TATA]TGAGAGTTTTGTTTA | 6709 |
rs550979846 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620722 | GAACTCCGTCTCAAA[A/C]AGAAAAAAAAAAGAC | 6709 |
rs550997455 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128553385 | CAGTGCTTGCATGGT[A/T]TGTGGCTCAAATCAA | 6709 |
rs551015397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594098 | ATCTTGGAGACACCT[C/T]GTGGTTTGCCTTTAT | 6709 |
rs551092720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567886 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGAATGT | 6709 |
rs551184557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605744 | CGTCTATAACCCCAG[C/T]ACTTTGGTAGGCCAA | 6709 |
rs551252780 | in-del | -/AAG | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607438 | TTTTAAAAAAATAAC[-/AAG]AAGTTTTTTAACACT | 6709 |
rs551363501 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614832 | AGTAAACTTTTTATA[C/G]TGGATTATATTAAAA | 6709 |
rs551368964 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584210 | AATGGAAAAAAGACC[A/T]TATCAATTTTTCTCT | 6709 |
rs551415122 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595206 | CTTCTGCCTCCCAGG[C/T]TCAAGTGATTCTCAT | 6709 |
rs551426543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607295 | AGGCATGAGCCACCA[C/T]GCCTGGCCAACAAAA | 6709 |
rs551460536 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621459 | GTTATTCTGCAGTGC[C/T]TATTTTTTCTGCATT | 6709 |
rs551506018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614259 | CAGGAGTTCAAGACC[A/G]GCCTGGGCAACATGA | 6709 |
rs551506340 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590483 | CCGAGACAGGAGGAT[C/T]GCTTGAGCCCAGGAG | 6709 |
rs551516462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595341 | TCTTGAACTCCTGGC[C/T]TCAAGTGATCTGCCC | 6709 |
rs551546029 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608551 | AGGAAGATGTAAAAC[A/T]GTTTGATTTATACGT | 6709 |
rs551594202 | snp | A/G | 0.000265475 | 0.0115181 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627643 | TGGCAACGCCTGGTC[A/G]GGCTCTGGAGCCGGG | 6709 |
rs551595039 | in-del | -/GA | 0.00115536 | 0.0240072 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593054 | AACTGTGAGTAGGCT[-/GA]GAGTCTTGCAGAGCA | 6709 |
rs551595660 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628144 | GTCCCCGATAGAGCC[G/T]TCAAGCCAGGGGGAG | 6709 |
rs551658063 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566339 | GGGATTACAAGTGTG[C/T]GCCACCGCACCCCCT | 6709 |
rs551663711 | snp | C/T | 3.35965e-05 | 0.00409843 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128626579 | CTTCAACCAGCTGGC[C/T]GAGCTGGACCGCCAG | 6709 |
rs551677049 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570621 | GGGATTACAGGCTTG[A/G]GCCACCGTGCCCAGC | 6709 |
rs551679491 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562059 | AGTGGAGACTTCTGA[A/T]TCAGAAAGACTTCAT | 6709 |
rs551683341 | snp | C/T | 6.59467e-05 | 0.00574187 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128587653 | AGATCTCAGTGCCTA[C/T]GGCAGCAGCATCCAG | 6709 |
rs551685155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594697 | TCAGGCTCCCAAAGT[A/G]CTGGGATTATAGGCA | 6709 |
rs551719041 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577041 | TGCTGGTGAGCTGTC[A/G]AGGCTGACTAGGCCT | 6709 |
rs551719057 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614905 | GCATGATTTTGCAAC[A/G]TCATGCATGGCTCAT | 6709 |
rs551723819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628502 | GGCAAAAATGCACCC[A/G]TTATGTGATAGACAG | 6709 |
rs551786950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622776 | ATTTATTTTTTAGAC[A/G]GAGTCTCACTCTGTG | 6709 |
rs551805031 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629202 | GGTTTTTCTCCTTAT[C/T]TCTCTTCTTACCTCA | 6709 |
rs551831313 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581280 | TTTCAGATTAGTGTG[A/T]TGTAAAATGTTTTAT | 6709 |
rs551905640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597711 | TGGAGTGCAGTGGCA[C/T]GATTTTGGCTCACTG | 6709 |
rs551906043 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602209 | TTTTTTTGTTTTTTT[G/T]GGGTTTTTTTTGTTT | 6709 |
rs551915056 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, missense | SPTAN1, WDR34 | GRCh38.p7 | 9:128633757 | CCTCAGGCCGCCACC[G/T]CTGCTGCCAGGCAGT | 6709 |
rs551932814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128555408 | AGTCCAGGTATTTGA[C/T]GAGCATGCAGAAAAC | 6709 |
rs551984635 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569178 | TAACATTTATAAGTG[A/G]CAGTGAGATGGCAGA | 6709 |
rs552021457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566345 | ACAAGTGTGCGCCAC[C/T]GCACCCCCTGCTTGA | 6709 |
rs552049481 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616651 | AGGCGCCTGTGGTCC[C/T]AGCTGCTTGTGAGGC | 6709 |
rs552051951 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633461 | GAATAAGACTTAGGA[A/G]AAAATGGTGCTTCAC | 6709 |
rs552085576 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570806 | GGATTACAGGCATGC[A/G]CTGTGCCACCACAGC | 6709 |
rs552202114 | in-del | -/A | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614600 | TCTCAAAAAAAAAAC[-/A]AAAAAAAAAACACAA | 6709 |
rs552260526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563635 | ATGGAGCTCTCTCCC[C/T]ACCCCTTACAAATGA | 6709 |
rs552262522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128556611 | TCTGGATTTTGATGC[A/G]ATGCAGTATGAATCT | 6709 |
rs552288164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564506 | AAGCATCACTTGAAC[C/T]AGGGAGGTCGAGGTT | 6709 |
rs552299495 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128553141 | ACTTCTGCAGCTCGT[G/T]CTTCCGAATCGCACC | 6709 |
rs552321659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557281 | GTGCATTCAACTTGC[C/T]GAAAGAATGGCAATC | 6709 |
rs552386079 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618362 | GAATCACACATGAAT[C/G]ACACATGAATCACAC | 6709 |
rs552426805 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572196 | CTGTACTTCATTCCT[G/T]TCTTCTTTGCTTAAT | 6709 |
rs552452166 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611501 | AGTTCATCTACTCCT[C/G]AGCTAGTACATTTCC | 6709 |
rs552462646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629755 | TGGGGTTTAGTCACA[A/G]CCATCTCTCTCCTTT | 6709 |
rs552481525 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570064 | TATCTTCCCATCTTC[A/T]CACTATTTTATATAC | 6709 |
rs552561302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611450 | ACTCCAGCCTGGGCA[A/G]CTGAGCAAGACCCTG | 6709 |
rs552585180 | snp | A/G | 3.31378e-05 | 0.00407036 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605480 | TTAGCGATTTCCGGT[A/G]CGGAGCCATGTTCAC | 6709 |
rs552613874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571534 | AGGTTGAAGTGAGCC[A/G]AGATCCTGCCATTGC | 6709 |
rs552623597 | snp | A/G | 6.59152e-05 | 0.00574049 | missense | SPTAN1 | GRCh38.p7 | 9:128605093 | CTCTAAACACAGACA[A/G]TTATGGACATGATCT | 6709 |
rs552731312 | in-del | -/AG | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571754 | TAGAAACTGAGTCTC[-/AG]AGAATTTGAGTAACT | 6709 |
rs552805006 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618697 | ACCGTCTTAGCCAGG[A/C]TGGTCTCGATCTCCT | 6709 |
rs552819333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572586 | TTGAGCAGGAGCTCT[C/T]ATTTAATCTTTTACT | 6709 |
rs552923565 | snp | A/G | 0.00557542 | 0.0525036 | downstream-variant-500B, intron-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128634094 | AGCCACAGTGGCTTT[A/G]AGTTGGGTTGCTGGA | 6709 |
rs552950593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585683 | ACACAGAGAAAACTT[A/G]TTTTTGTCCTTCTGT | 6709 |
rs552970547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591931 | TTTCAGATACTCTAC[A/G]CCCCTACAGCTCTGT | 6709 |
rs553072219 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632068 | GCAGTAAGTGGCTCC[C/T]GGGCTGGTGACTGAG | 6709 |
rs553118492 | snp | C/T | 0.00134852 | 0.0259315 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624529 | GAGCCTTCCCAGAGC[C/T]GCTCTTTGTCTCCTT | 6709 |
rs553135496 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128556253 | AACAGCTCTCTTTAT[A/G]TGTTTTCTTTGTGTA | 6709 |
rs553140191 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620285 | TGAGCCACCTTCCTC[A/T]CCATGGGAAGCATCC | 6709 |
rs553327813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554659 | ATCCCACTAGTTACG[C/T]ACTCATCTGTTGCAG | 6709 |
rs553442880 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595012 | ATGAGGTTTCACCAT[A/G]TTGGTCAGGCTGGTC | 6709 |
rs553483624 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587174 | CCCTACAGCTTTGAC[C/G]TCCTGTGCTCAGCAG | 6709 |
rs553523917 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569042 | CTTAAGAAGTTACCC[A/G]AATCCTGCCTTTGTA | 6709 |
rs553540351 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560875 | ACAAAAATTAGTCGC[G/T]TGTGGTGGCGGGTGC | 6709 |
rs553560692 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597939 | CAGGCGTGAGCCACC[A/G]CACCCGGCCTGTTTT | 6709 |
rs553577211 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620766 | CCTTTTCTGAGATGT[A/G/T]TTCAAGTTAAACCTT | 6709 |
rs553590994 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601187 | AGGGTTTCCCTGTGT[C/T]AGCCAGGCTGGTCTC | 6709 |
rs553640705 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624039 | AGTGAGCCGAGATCA[C/T]GCCACTGCATTCCAG | 6709 |
rs553640938 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587383 | AGCCTCTGTGCCTAG[A/G]CCAGGATGAGTAAGC | 6709 |
rs553715609 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128551218 | TGCAGAGCTCCCCGT[C/T]TGCCTGACTGCACAG | 6709 |
rs553715700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559982 | TCAGGTGATCCACCC[A/G]CCTTGGCCTCCCAAA | 6709 |
rs553754499 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601664 | AACAAAAAGTAAAAA[A/G]AAATTTTAAAAGTGT | 6709 |
rs553807725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567331 | AGTTGCGCTCATGTC[A/G]CCCAGGCTGGAGTGC | 6709 |
rs553876747 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626337 | CCACCTCCTGCACTG[C/T]GTCGGCACGTCCAGC | 6709 |
rs553945609 | snp | A/G | 1.64808e-05 | 0.00287057 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128583879 | AGTAGAAGGTCACTT[A/G]GCTTCGGATGATTAC | 6709 |
rs553951462 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575737 | CTTTTTTATTTGAAG[C/G]TTCCCTGGGCTCTCT | 6709 |
rs553976503 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578616 | CGGGTGGATCATGAG[A/G]TCAAGAGATCAAGAC | 6709 |
rs553983141 | snp | G/T | 0.0364509 | 0.129988 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606498 | ATATATTTTTTTTTT[G/T]GGGGGGGAAGCGTTT | 6709 |
rs554045370 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621041 | CCTCTTCCCCAGCTA[G/T]ACTGTAATGTGTGCA | 6709 |
rs554046432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606893 | GTGTTGTGCAGCCAC[C/T]CCTCTCTAGTTTTGG | 6709 |
rs554125355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562450 | GTGGGAGAGGAGAGT[A/G]CACTCCTGGGAAAGG | 6709 |
rs554161838 | in-del | -/AATT | 0.000577934 | 0.0169892 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632722 | GGATCCGAACAGGTA[-/AATT]AATTAAGGCCAGGTG | 6709 |
rs554198533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628789 | CAGAGCAGCTGGGGA[C/T]GTAGGGATCGCAGTT | 6709 |
rs554257149 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590863 | TCCAATAAAAAAGAG[A/T]TCTAACTCAATGAAA | 6709 |
rs554257792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623204 | TGGGACCACAGGTGG[A/G]TGTCAACACACCTGG | 6709 |
rs554266542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569518 | CGTTTCACATATCTA[A/G]TATGAAGATATTAAG | 6709 |
rs554297600 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612598 | AGTCATGTATTCTCC[A/G]TGGAGAATGTTTGGA | 6709 |
rs554384831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622461 | TGTGCCACTATGCCC[A/G]GCTAATTTTGTATTG | 6709 |
rs554385332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628261 | GCCCTAAGAACCCCC[A/G]TGCCTGTCCAGCCAC | 6709 |
rs554408202 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585278 | AGGTGATCCACCTAC[C/G]TCGGCCTCCCAAAGT | 6709 |
rs554421767 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589521 | GACCTCGTGATCCAC[A/C]CACCTCAGCCTCCCA | 6709 |
rs554446121 | snp | A/G | | | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128550681 | TGCCCCTCAGTCCCA[A/G]GGTGCTTTCTTTGCT | 6709 |
rs554491722 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629481 | CTAACCCTGGCTCGC[C/T]GGGTTTTAAAAGGGT | 6709 |
rs554518701 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563142 | AGAAAATAGGCCAGT[A/G]CAGTGGCTCATGCTT | 6709 |
rs554521382 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128550953 | AGCTTCTGGGGTGTG[A/G]TCACTGCTTTTCTCT | 6709 |
rs554522191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627836 | CTTTTGTTTTCCTTT[C/T]TTTCTTGTGTCTTCT | 6709 |
rs554555578 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596273 | GTTTTGTTCGTTTTT[G/T]TTGTTTGTTTGTTTG | 6709 |
rs554589403 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617526 | CAGAAAACTGGCAAG[G/T]ATTTTCCCAGAAAGA | 6709 |
rs554601689 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595234 | CATGCCTCAGCCACC[C/T]GAGTAGCTGGGATTA | 6709 |
rs554679769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592777 | CGCCAGGAAAATGAA[A/G]GTGAACTAACCCTCT | 6709 |
rs554701451 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596695 | AAATTTTATCTCGTT[C/T]TTATTTATTTTTTAG | 6709 |
rs554720557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558223 | TTTATTACAATAGAG[A/G]ACATAGTTGTAATTC | 6709 |
rs554731574 | in-del | -/A | 0.000741125 | 0.0192357 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607722 | GTGGACCTGCCTGCT[-/A]GAGTAGCAAAGACGT | 6709 |
rs554745428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577736 | ATTCTGCATCACTGC[A/G]TTATGATTGATAGAA | 6709 |
rs554762887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590815 | AAGATCGTGCCACTG[C/T]ACTCCAGCCTGGCAA | 6709 |
rs554774594 | in-del | -/A | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574910 | AGTGTTAGCACAGAT[-/A]ACGGCCATTTTAAGT | 6709 |
rs554828882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610783 | CCAGTAAAATAAATT[C/T]CTTCCTGCAGTCAAG | 6709 |
rs554856232 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128555976 | CCTGTAATCCCAGCG[A/C]TTTGGGAGGCTAAGG | 6709 |
rs554867323 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620434 | TAAGGAAAAGACCTG[A/G]GGCCAGGTGCGGTGG | 6709 |
rs554868364 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624809 | GCCCTGGTCAGGGGC[A/G]CCACCCAGCTCCTGG | 6709 |
rs554911638 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592242 | TATAGATTCTGTTAC[G/T]ATAGAGATAAGAATG | 6709 |
rs554916533 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128556874 | AGTTAATTTTGTTTG[A/G]TCTGAGAATCAACTG | 6709 |
rs554935935 | snp | C/T | 3.43979e-05 | 0.00414702 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630168 | CCTCGATCCCTGGGG[C/T]CCATTAGGTAAAGAT | 6709 |
rs554971766 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586175 | CCAGGCTGGACTGCA[A/G]TGTTACAATTGTGGC | 6709 |
rs554979989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599469 | GCCATTCTCCAAAAG[A/C]CAAAAAAAGTTGGTT | 6709 |
rs555026903 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605828 | GAAATGCCGTCTCTA[A/C]CAAAAGTACAAAAAT | 6709 |
rs555061899 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560035 | CCACCCTGCCTGGCC[G/T]ATAATTTTGATTTTT | 6709 |
rs555145124 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580862 | GGATAGCTGTTCTGT[C/T]TGCCTCGGAGGCATT | 6709 |
rs555147079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572664 | GTCCCCTAACTCAGT[A/G]CCTTAGTTTGGCAGA | 6709 |
rs555165162 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603879 | CAGTAATGCAGTGAG[C/T]GGCTTCCTTGCCGCC | 6709 |
rs555169578 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598843 | CTGGACATTTGGACT[A/G]GCATTTCCATTTGTC | 6709 |
rs555172473 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612938 | TCAAAAAAAAAAAAT[G/T]TTTTTTTTTAATAAT | 6709 |
rs555178787 | snp | C/G | | | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128612114 | TGTTCCCCAGGCCCG[C/G]CTGGCTGCCTTAGCT | 6709 |
rs555199099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566166 | GGCTCAGGTGATCCT[C/T]CTGCCTTAGCCTCCT | 6709 |
rs555226649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604531 | GGCTCTTACTGATGT[C/T]TATTTGTGACATGGG | 6709 |
rs555244439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609772 | GGTTTGCTGGTGTCT[C/T]TTCATCCATCCTTTT | 6709 |
rs555281416 | in-del | -/TTTTGTTTTGT | 0.00953873 | 0.0683987 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597641 | AGCTTTTTTTGTTTG[-/TTTTGTTTTGT]TTTTGTTTTGTTTTT | 6709 |
rs555282281 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580039 | TTTATAAAATGATAC[A/G]TAGGCCAGGTGTGGT | 6709 |
rs555321645 | snp | A/G/T | 0.000116401 | 0.00762811 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621136 | GGCTCTCAATAGTGT[A/G/T]CCTTGGCTGCTTCTA | 6709 |
rs555367144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606310 | GAACCTGGAGGCGGA[A/G]GTTGCAGTGAGCCGA | 6709 |
rs555372194 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564250 | ATGGTGAAACCCCGT[C/G]TCTACTAAAAATACA | 6709 |
rs555397115 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626743 | GAGCCCTCTCTGGGC[C/G]CTGCTCAGAGCCCAC | 6709 |
rs555407895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565487 | TCTACACTTCTCCAG[A/G]AAGGTGGTCTCTTAG | 6709 |
rs555451095 | snp | C/T | 1.66804e-05 | 0.00288789 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625994 | GTGAGGATGGGGCCA[C/T]GTGAAGCTTAGCTGG | 6709 |
rs555459234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620441 | AAGACCTGGGGCCAG[A/G]TGCGGTGGCTCACAC | 6709 |
rs555463680 | in-del | -/GAG | 5.43907e-05 | 0.00521463 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628091 | TTCTCGTCACCTGAT[-/GAG]GAGTGTGTGCCTTGC | 6709 |
rs555464416 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594982 | GCCTGGCTAGTTTTT[A/G]TATTTTTAGTAGAGA | 6709 |
rs555480308 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573022 | CATGTTGACTGTCAC[A/G]TGGTTTTCAGGTTTT | 6709 |
rs555574401 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589433 | AGCTGGGACTACAGG[C/T]GCCCACCACTGCACC | 6709 |
rs555637426 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593657 | AAACTTTCTGAGAGC[C/T]GAATGTATCATTTTA | 6709 |
rs555670579 | snp | C/T | 6.83519e-05 | 0.00584562 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632095 | TGAGCTGAGGGCCCC[C/T]GTCTGAGCATCTGTG | 6709 |
rs555704820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587948 | CCTCCTGGGTTCAAG[C/T]GATTTTCCTGACTCA | 6709 |
rs555763619 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587170 | GACTCCCTACAGCTT[C/T]GACCTCCTGTGCTCA | 6709 |
rs555806176 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574912 | GTGTTAGCACAGATA[C/T]GGCCATTTTAAGTAA | 6709 |
rs555820599 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604176 | CTCTTACTGGAATAT[G/T]GTATACTAATTTATT | 6709 |
rs555847475 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589566 | CAGGCATGAGCCGCC[A/G]TGCCCGGCCTTTTTT | 6709 |
rs555942992 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574008 | TCTGCCCGCCTCGGC[C/G]TCCCAAAGTGCTGGA | 6709 |
rs555969051 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589953 | CTGTGACCTCACCCC[A/G]CAGGCTTTGTCTTCT | 6709 |
rs556030395 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594402 | TCAGGCTCAGCTGAA[A/C]ATTTGTTTAAAGATT | 6709 |
rs556044801 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561430 | GCTCTTTTGGAGGCC[A/G]AGGCAGGCAGATCAC | 6709 |
rs556051376 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128552302 | AGTGACCTCACTGCA[C/T]CATCACCCCTCACCC | 6709 |
rs556112512 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128552752 | CCCGGGCAGCCGACC[C/G]CCGGGTGGGAGCTGG | 6709 |
rs556114232 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633585 | TCGAAGCAGCTGGCT[A/C]CTCCCCTTGTTCTCT | 6709 |
rs556114897 | snp | A/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128627434 | CGGCAGGAGGAGAAC[A/G]ACAAGCTGCGCCAGG | 6709 |
rs556146771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590137 | CTTGGCCATTTTTAA[A/G]AGCAAGTTTATTCCC | 6709 |
rs556155724 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596140 | TGAGCCACCGCACCC[A/G]GCCCATAATGTTTTC | 6709 |
rs556179611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554782 | TCATCACTGGGGGCC[A/G]CTTGACTGGAGCAGC | 6709 |
rs556188544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606975 | TCTCTTCCCCACCCA[C/T]TAGGAATCCTTTATC | 6709 |
rs556217182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561378 | TCCATCTCAAAAAAA[A/G]AAAGGCCAGGCGCGG | 6709 |
rs556344772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569566 | ACAGTGAGGTGTGCA[C/T]GTTGAGTTTCTTATA | 6709 |
rs556348899 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577588 | AGTTAAGGGTCTGTT[C/G]TGTGTTCTGTGAAAG | 6709 |
rs556354274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562572 | CTGGAAGGTGACTGA[A/G]TGAAGTCTTGTTTAC | 6709 |
rs556365639 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601053 | CAGTGGCACGATCTC[A/G]GCTCACTGCAACCTC | 6709 |
rs556425169 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615047 | TCACATATTAGGAAG[C/G]CTTCAGGCTCCTGGT | 6709 |
rs556432318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601863 | ACTATTCTCCTCATT[A/G]AGTAGATTTCTAACT | 6709 |
rs556484844 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576606 | TTATAGACTAACCAC[A/G]CTACTCCAAAAGATA | 6709 |
rs556488594 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603163 | GTTAAACAGTCTCAG[A/C]TGCCAGCATTTGTTA | 6709 |
rs556522946 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608450 | TCTGAGATTTTAATA[A/T]TGGGGGTGCCACAGG | 6709 |
rs556581163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610972 | TATGAATTTTGCTTA[A/G]TGGTGATTTCTGCTT | 6709 |
rs556644627 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578636 | GAGATCAAGACCATC[C/T]ATGCCAACATGGTGA | 6709 |
rs556652224 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563173 | GTAATCCCAGCACTT[G/T]GGGAGACTGAGGCAT | 6709 |
rs556685444 | in-del | -/G | 0.00358779 | 0.0422022 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628484 | CTGTCCGCCCTAATA[-/G]AAGGCAAAAATGCAC | 6709 |
rs556696621 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591366 | CCACTGTGGCCGGCC[A/G]TTTTGGACCTCTTAA | 6709 |
rs556699460 | in-del | -/TT | | | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128551547 | CCTGGGCCAAGAGAC[-/TT]AGCCTACATGAGCAT | 6709 |
rs556734889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629947 | CCTGAGGTCTCCTGT[C/T]TGTCAGGTGTCAGGG | 6709 |
rs556761229 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554142 | AAATTAACAATAAGC[C/G]TTTTTTAGTAACTGG | 6709 |
rs556767629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586010 | CCAGGGAAGTGGAAC[A/G]GGGCTTGTACTGAGA | 6709 |
rs556768672 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628291 | CCGGGCTCTGTTGGG[C/G]TCTCACCTCTGCTTC | 6709 |
rs556773400 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616243 | TTTCTGAGATGGAGT[C/G]TCGCTCTGTCACCAG | 6709 |
rs556775430 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623030 | TGCTGGGATTACAGG[C/T]GTGAGCTACTGTACC | 6709 |
rs556784804 | in-del | -/T/TT | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572022 | AAGCACACTGAGCTA[-/T/TT]TTTTTTTTGTATTTT | 6709 |
rs556796231 | snp | A/G | 6.66145e-05 | 0.00577086 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128624438 | GCTGGATGAGAACTC[A/G]GCCTTCCTTCAGTTC | 6709 |
rs556933371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557563 | TTTTTTATTTTTATA[C/T]TCCCAAATTTTATGC | 6709 |
rs557000201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578422 | TACCTGCTTCTGATA[A/G]AGGCTTAACTGGGTT | 6709 |
rs557045933 | in-del | -/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560630 | GGTGATCTGCCCGCC[-/T]TCGCCTCCCAAAGTA | 6709 |
rs557097779 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570897 | AACTCCCAACCTCAG[A/G]TGATCTGCCCGCCTT | 6709 |
rs557103045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629366 | GGGGGGCATTTTCCC[C/T]GGGGGGACATGGCGT | 6709 |
rs557133201 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128551080 | GGAAAGAAGCCAAAC[G/T]GCAGAGGGCCAGGAA | 6709 |
rs557139634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585331 | ACCGCGCCTGGCTCC[A/G]AGCCTGAATTTCTTA | 6709 |
rs557241146 | snp | A/G | 3.30142e-05 | 0.00406276 | missense | SPTAN1 | GRCh38.p7 | 9:128605449 | TTGGGTGACTCCCAC[A/G]ACCTGCAGCGCTTCC | 6709 |
rs557269857 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558933 | CCTTTTAGGAGCAAA[A/C]AGAAACTGGAACTCG | 6709 |
rs557304515 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598676 | ACTTCTTTATACCCA[C/T]ATCCCTCACTTTCAC | 6709 |
rs557306645 | snp | A/G | 1.65048e-05 | 0.00287265 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128625158 | AGACCTGTCTTCTGT[A/G]CAGACGCTCCTCACC | 6709 |
rs557326282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561197 | ATAGTGAAAGCCTGT[C/T]TCTTAAAAAGAAGAG | 6709 |
rs557339353 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128555541 | GTTTCTGTTAAACAA[A/G]TTGGTTAGGATTTGT | 6709 |
rs557348808 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594579 | GGGATTACAGATGTG[C/T]GTCACCACGCCCTGC | 6709 |
rs557351249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586722 | TATCTGTTTTTTGAC[C/T]AAAATTCTCAAATTT | 6709 |
rs557406262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567173 | TATTAATTGTCTTTT[C/T]TGGATGCTTTAAACT | 6709 |
rs557425310 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600175 | ATCATGAAATATGTC[A/C]TTTTCTGGTGTGCCT | 6709 |
rs557448338 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128552084 | TCTCACCCTTTGGGA[C/T]TGGGCGTTTTTCCGG | 6709 |
rs557452447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630831 | TGCCTCAACCTCCCA[A/G]GTAGCTGGGATTACA | 6709 |
rs557465841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560742 | GAGGGAGTGAAGGCC[A/G]GGTGCTGTGGCTCAC | 6709 |
rs557466141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128552976 | CCGGGTCCCTCCCAA[C/T]CACCCCCAAGCCTGG | 6709 |
rs557485405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592877 | CTCCATAGTTTCCCA[A/G]CATTAAGCATCCACC | 6709 |
rs557545175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566244 | TGTATTTTTAGTAGA[A/G]ACGGTGTTTCACCTT | 6709 |
rs557558599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598051 | CCTACCGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 6709 |
rs557561912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606458 | TGCCATATGACATTA[C/T]ATTTTTCCCTAGACA | 6709 |
rs557633372 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567845 | AGCTCACTGCAACCT[C/G]TGCCTCCCAGATTCA | 6709 |
rs557639946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604800 | GCTGGGCATGGTGGT[A/G]GGCGCCTGTAATCCT | 6709 |
rs557656395 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598031 | TCAGCTCACCGCAAC[C/T]TCTGCCTACCGGGTT | 6709 |
rs557656915 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564628 | AATATTAGGTTGCTC[A/G]GTGTAATCATACCTT | 6709 |
rs557702290 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615177 | TTATTTATTCTGGAC[C/T]GAGTATCTGTGAGAT | 6709 |
rs557766209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600828 | CCACCATGCCTGGCA[A/G]ATTTTTGTATTTTTA | 6709 |
rs557839079 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614573 | CCAGCCTGGGCGACA[A/G]AATGAGACTACGTCT | 6709 |
rs557873720 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597211 | GATAGGGGTCTGGTT[A/G]TGTTGCCCTAAGCTG | 6709 |
rs557947514 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561108 | GGCACGGTGGTTCAC[A/G]CCTGTAATCCCAGCA | 6709 |
rs557953381 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613094 | TCCACACTGCTGATT[A/C]TTTCCTAGGGGGGTT | 6709 |
rs557955177 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620188 | AAAGGAGATGCTGCA[A/G]AGTATCATGGTCAGA | 6709 |
rs557964933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605924 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 6709 |
rs558009277 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587966 | TTTTCCTGACTCAGC[C/T]TCCTGAGTAGGTGGG | 6709 |
rs558024865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562390 | ACAGGCGTGAGCCAC[C/T]GCGCCCAGCCGAGAT | 6709 |
rs558025507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594909 | TCTCGGCTCACTGCA[A/G]CTCCTCCTCCCAGGT | 6709 |
rs558075977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581597 | TAGGATTTCATGATA[C/T]GGCTGGATTGATTTT | 6709 |
rs558089748 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582324 | AAAATCTCAAAAGTT[A/T]TGAGAAAAAATGTCA | 6709 |
rs558096311 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558602 | AAGATTGGAGTTTGT[G/T]TTTTAATGGCACGTT | 6709 |
rs558154123 | snp | G/T | 0.000922084 | 0.0214521 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607590 | AGCTATTTTTCTGGG[G/T]TGCTGGTTTCCAGGG | 6709 |
rs558190565 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626019 | AGCTGGCCCACAGCT[C/T]AAGGAAGGACGCCCA | 6709 |
rs558239344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621892 | TGAAGGCAGTGTGTC[C/T]GTGGGTCGGGAATTC | 6709 |
rs558250544 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128634125 | GGGAAGCCGTCCTTA[C/T]CCCCATGTGTGGTCT | 6709 |
rs558280047 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575652 | TCAGGGTTTCTCAGA[C/G/T]GAGGGTGTGGTGGTG | 6709 |
rs558351110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596542 | CGGTCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 6709 |
rs558370339 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128633117 | CTGCTTGTAGAAGCA[G/T]CTCCGAGCCCCCAGC | 6709 |
rs558378872 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627765 | GCGTGGTCAGCCCCA[G/T]CCATGACTTGGTGAC | 6709 |
rs558389009 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128553847 | AAGTATTTTCATAAT[A/G]TGTTGAGAAATTGCG | 6709 |
rs558449802 | snp | C/T | 3.38101e-05 | 0.00411143 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632174 | TCAGCTCAAAAAGAT[C/T]GAGGACCTGGGGGCC | 6709 |
rs558527631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558120 | ATATTAGAAATTTCT[A/G]GCCAAGATTCATATA | 6709 |
rs558590143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584627 | GTCGAATTTAAATTA[C/T]TGAACTGGAACCATG | 6709 |
rs558595036 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613255 | GAATCACAGTAACAC[A/G]TTGTGATGGAGAAGT | 6709 |
rs558661631 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557656 | CAAACAGCTGTCTCT[C/T]GGCGTTCATCAATAA | 6709 |
rs558666887 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590224 | TCTTTCTATTGAGTC[A/T]AATTTAAACCTAAAC | 6709 |
rs558676225 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602426 | TTCGCCAAGTTGGCC[A/C]GGCTGGTATTGATCT | 6709 |
rs558734853 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596247 | ACTACACATTGTTTT[G/T]GGGTTTTTTTGTTTT | 6709 |
rs558756418 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604430 | CAGGTGAGGGGTCAG[C/T]CCTGGGCTGGGAGAG | 6709 |
rs558816645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571989 | AGCCTCCCGAGTAGC[C/T]GGCACCACAGGAACG | 6709 |
rs558826774 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574288 | TTAATAGTATCAATT[A/G]TGTACCTATTATTAT | 6709 |
rs558865577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569397 | TATTGGTCAATGACC[A/G]TGGTGATGGGACTGA | 6709 |
rs558867199 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561854 | GCAGTTTCTTTATTT[C/G]CAAGCTCTGAATATA | 6709 |
rs558894945 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571003 | AATACTGTTAACTGG[C/G]CGGGCATGGGGCTCA | 6709 |
rs558897278 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604853 | GGAGAATCACTTGAA[C/G]CCGGTGGGGGCGGAG | 6709 |
rs558993543 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623560 | TCCCAGGTTCAAGCA[A/G]TTCTCATCCCTCAGC | 6709 |
rs559032935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578302 | CTTATAATGCACCAG[C/T]TTATCAGTGTTGGGT | 6709 |
rs559102357 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611011 | GAAATGTCCATATGT[A/G]TCTCATTCATTACAG | 6709 |
rs559113494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598073 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 6709 |
rs559172835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610144 | GAACAGCTAGAGAAC[C/T]GTAGAGAGACGGATG | 6709 |
rs559182169 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599143 | CCAAAAATTGATTTC[-/T]TTTTTTTTTGAGACG | 6709 |
rs559227271 | snp | A/T | 0.000365965 | 0.0135222 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609691 | AATTTTTTTAAGAGT[A/T]GTAGTTAAATGAGCT | 6709 |
rs559283575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571311 | AAAAAAAGGCCAGGC[A/G]CAGTGGCTCATGCCT | 6709 |
rs559374138 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629255 | TTGACATCCCCAGGC[A/G]GCTCCACCCTGACTA | 6709 |
rs559374182 | snp | A/G | 1.7042e-05 | 0.00291903 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625231 | AGATAGCATCTGTGA[A/G]ATGACTGGTGGCGTC | 6709 |
rs559378879 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558454 | CCTCCTTCAGTCTCT[A/C/G]TGTGAACAGACTTGA | 6709 |
rs559411147 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623883 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC | 6709 |
rs559431424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578483 | AAGCAAACAGACAAG[C/T]TCTGGCGAGATAGAA | 6709 |
rs559454365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564235 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCGTC | 6709 |
rs559474506 | in-del | -/ATTCCACCACTTAAAAGG | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596600 | ACACATTGTTTATCC[-/ATTCCACCACTTAAAAGG]ATTCTTACAACAAAT | 6709 |
rs559504750 | in-del | -/G | 1.65015e-05 | 0.00287237 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632533 | GGGTGTTCGGCAGCA[-/G]GGGCTGCCTGCTGAG | 6709 |
rs559517959 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564736 | GGGTACAGTTTAGTA[A/T]AGAGTCAGGATCCTG | 6709 |
rs559517970 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557865 | CTGGAGTGCAGTGGC[A/G]CGATCTCGGCTCACT | 6709 |
rs559605940 | snp | A/C | 1.64727e-05 | 0.00286986 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618826 | CTATCACAATCAAAG[A/C]TGGAGGAGATTATGG | 6709 |
rs559637016 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570880 | TAGTCAAGCTGGTCT[C/G]AAACTCCCAACCTCA | 6709 |
rs559699073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573617 | GTGTGCCACCATGCC[C/T]GGCTAATTTATGTAT | 6709 |
rs559731941 | snp | C/G | 1.67242e-05 | 0.00289168 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581944 | TTATAGTAAGCCAGA[C/G]TCTTTTTCCCTGGAA | 6709 |
rs559743360 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598099 | GATTACAGGCATGGA[A/C]CCCCACACCCAGCTA | 6709 |
rs559757395 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565920 | TTTCCTGACATTTTT[A/G]GTCACTTTAGGAAAT | 6709 |
rs559760483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612329 | AGTGCCCAAAACCAC[A/G]AAAAGGCAGGGCTCA | 6709 |
rs559837602 | in-del | -/TT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594822 | TTTTTTTTTTTTTTT[-/TT]CAATTTTTTTTTTTT | 6709 |
rs559839676 | snp | C/G | 0.000543527 | 0.0164763 | missense | SPTAN1 | GRCh38.p7 | 9:128594194 | CATTCTCTGCTGGAA[C/G]TGGGTGAGAAGCGTA | 6709 |
rs559860463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580327 | TGTATATATATACAT[A/G]TTTTATTTTACTTTT | 6709 |
rs559887729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624674 | GCCAGAACTGCCACC[C/T]GGAACTGGGCTGGCA | 6709 |
rs559938189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586369 | AACTCCTGGCCTCAA[A/G]CAATCCTCCTGCCAA | 6709 |
rs559981894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559628 | ATGCATAATTTCTCA[A/G]TGTTTTTCCATCTTA | 6709 |
rs560001826 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579375 | GAATGAAAGAGAGCT[C/G]AGACCCATGTGAATG | 6709 |
rs560004787 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581121 | GTGTTTTGCCTCCTC[A/G]GGTAGTGTGCTTGTT | 6709 |
rs560019135 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568759 | TGAGGCTCACTTCAA[A/G]GTCCGCCAACAGGGA | 6709 |
rs560047591 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588155 | GGCGCCCGCCACCAC[A/G]CCCAGCTAATTTTTG | 6709 |
rs560064469 | in-del | -/A | 0.354665 | 0.227036 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599685 | ACAAAGCACAGCTCT[-/A]AAAAAAAAAAAAAAA | 6709 |
rs560088870 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602053 | GAAATTTATTTTAGG[A/T]ACCTTTATAAATCCC | 6709 |
rs560179258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626893 | TACCATGGCTCCCTG[C/T]AGCCTCAACCTCCCA | 6709 |
rs560180275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594605 | CCTGCTAATTTTTGT[A/G]TTTTTTGGTAGAGAC | 6709 |
rs560187917 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128555935 | TGTTTAAAAAATAGC[G/T]CTCGGGCTGGGTGCG | 6709 |
rs560213432 | snp | C/G | 0.000741125 | 0.0192357 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607723 | GTGGACCTGCCTGCT[C/G]AGTAGCAAAGACGTG | 6709 |
rs560224958 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601404 | CTTGAGTTACAGGCA[A/T]GTTAGACAGCAGATT | 6709 |
rs560257877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631842 | TATAAAAATCTTTGG[C/T]CACTGCTTCCTGGAG | 6709 |
rs560282977 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568670 | ATGTATCCCTAACTA[C/G]AGGGAGCAGGATTGA | 6709 |
rs560311263 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572616 | TTTCATGCTCACAGT[C/T]ACTATGGTGATCTTG | 6709 |
rs560319155 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632300 | GCGCATGCAGCACAA[C/T]CTGGAGCAGCAGATC | 6709 |
rs560320788 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584030 | TATAGGAGGGAGGAA[A/G]AGCCAGTAATTTGAG | 6709 |
rs560351895 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599583 | CTTTTCACAGCTGCA[C/G]TTATAGCCTACTGCA | 6709 |
rs560385756 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128552975 | GCCGGGTCCCTCCCA[A/G]CCACCCCCAAGCCTG | 6709 |
rs560390110 | snp | G/T | 8.23988e-05 | 0.00641815 | missense | SPTAN1 | GRCh38.p7 | 9:128582508 | TGCAACCAAGCTAAT[G/T]CAGAACAACCACTAT | 6709 |
rs560411565 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561994 | CACAATAATTTCATG[C/G]CAGAATGTGGCAGTG | 6709 |
rs560468561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606050 | TCAATGTAAAATAGT[C/T]AAACTACTGAATGCC | 6709 |
rs560488097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128555148 | CTGCCAAGACCTGGG[A/G]ACCTTGGTTCTCCTT | 6709 |
rs560499917 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609339 | TATGTTATTGAGTAG[A/G]TTTTGTTAAATAAAG | 6709 |
rs560570709 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595718 | TTGCCATTCTCCCTA[A/C]CCCCAGTGGCCCACG | 6709 |
rs560598487 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554381 | ATGTCACAGGCTGCA[G/T]TGTAAGCCTGTCAAG | 6709 |
rs560599711 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622694 | CCCCCTTTCCACAGG[G/T]GTTAAAGAATTTCTC | 6709 |
rs560603134 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574480 | ACTTGAAGACCACCA[A/G]AAAACCACTGTGAAC | 6709 |
rs560631765 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578803 | CATTCCACTCCCGTC[C/T]GGACAACAAGAGTGT | 6709 |
rs560637424 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614038 | TGAATTCAGGTTGTG[G/T]TGTTTTGCATTGGAT | 6709 |
rs560664312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567670 | TCAGATATCAAAGAA[C/T]AAGTACTTAAAGTTA | 6709 |
rs560697300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616993 | CTATAATCCCAACAC[C/T]TTGGGAGACCGAGGT | 6709 |
rs560717208 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614257 | CCCAGGAGTTCAAGA[C/T]CAGCCTGGGCAACAT | 6709 |
rs560719289 | snp | A/G | 0.000103869 | 0.00720582 | missense | SPTAN1 | GRCh38.p7 | 9:128627417 | TGCAGAAGGAACAGC[A/G]GCGGCAGGAGGAGAA | 6709 |
rs560742709 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628427 | CCCCTAAGTAGCTGA[A/G]GCTGCCACTTTACTT | 6709 |
rs560761835 | snp | A/G | 8.23784e-05 | 0.00641735 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609078 | CACTTCCTTCTCCAC[A/G]GTAAGATATGCTCAT | 6709 |
rs560870587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590300 | GTAGAACTTTCTGTG[A/G]TGGTGGAAATGTAAG | 6709 |
rs560916394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608646 | TCTAACACCTGCCCC[A/G]CCTGAGTGACCTGGA | 6709 |
rs561051992 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616494 | GTTTGTGGCCGGGCG[C/T]AGTGGCTCACGCCTG | 6709 |
rs561079045 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584098 | TTCTTAGATCGCTCT[G/T]TGCTGCATGTGCTTC | 6709 |
rs561080096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569860 | GTCTCACGTTTGCTT[A/G]GCAATACTCTACAGT | 6709 |
rs561088530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576076 | CACAGTGACAGATGT[A/G]TTGCTTTTCCAAACC | 6709 |
rs561169602 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601763 | GTCCACCTTTGAACC[C/T]GCTCAGTCACCTTGT | 6709 |
rs561184891 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613967 | CCAAGATCGCGCCAC[A/G]GCACTCCAGCCTAGG | 6709 |
rs561198845 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580191 | TGGTGGCACATTCCT[A/G]TAGTCCGAGCTACTT | 6709 |
rs561200872 | snp | C/T | 4.9666e-05 | 0.00498302 | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633369 | ACCCCTCGCTGCTTG[C/T]CCTGCGTCGCCTTGC | 6709 |
rs561215397 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128556487 | GTCATAGTAACAATA[A/T]GGAACTTAAATACCT | 6709 |
rs561258898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623959 | TGGTGGTGTTCGCCT[A/G]TTAGTCCCAGCTACT | 6709 |
rs561276856 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557141 | TTTCCATAACCAAAT[C/G]ACCAAACGACCCGTT | 6709 |
rs561330541 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629016 | CCCGCCGGGCACCAG[A/G]TTGCCCTTGCCTGCG | 6709 |
rs561393353 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629568 | ACGCACCGTGTGATT[C/T]GTCCCTGCACGTAAC | 6709 |
rs561408615 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128556866 | TGGTTTTGAGTTAAT[A/T]TTGTTTGATCTGAGA | 6709 |
rs561439486 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596831 | GAGTGGCTGGGACTA[C/T]GCACATAGGCTACCA | 6709 |
rs561468959 | in-del | -/CA | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613998 | AACAGAGCAAGACTC[-/CA]CATCTCAAAAAAAAA | 6709 |
rs561501723 | snp | G/T | 0 | 0 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597438 | TTGAGGTAGGAGGAT[G/T]GCTTGAGCCTGGGAG | 6709 |
rs561564501 | snp | A/C/G | 0.000164084 | 0.00905638 | missense, intron-variant | SPTAN1 | GRCh38.p7 | 9:128592988 | CTCTGTGCAGGACAC[A/C/G]CATAACTAAGGAGGC | 6709 |
rs561569193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603302 | GTGGTTTTTACCATT[C/T]TTTTTTCACTCTTCA | 6709 |
rs561598177 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558537 | CATTCCTAGGAAGTC[C/G]TCTCTGTTGTGGTTT | 6709 |
rs561661030 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128551421 | CCCCAGCAGCCACCC[A/G]CATCAAAATGCCTCC | 6709 |
rs561721665 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564669 | TACAATTGCTTTGCA[A/T]ATCTATAGAGAAGTG | 6709 |
rs561742043 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565000 | AAGAGGTGGGTTCTT[G/T]CTTCTGTCTGAAGGA | 6709 |
rs561771165 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588160 | CCGCCACCACGCCCA[A/G]CTAATTTTTGTATTT | 6709 |
rs561909965 | in-del | -/TGTT | 0.0011988 | 0.0244533 | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633620 | ACCCTCCCCCAAATC[-/TGTT]TGTTTTCATGTAAAA | 6709 |
rs561920573 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624546 | CTCTTTGTCTCCTTC[C/T]GTGTCATTGGTTTTC | 6709 |
rs561937921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619070 | CTGGTCATCATTTCC[C/T]TGTTGGTTTGTTAGA | 6709 |
rs561945197 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562668 | ATAGGCTGACAGACT[C/T]AGGGCAGCAGTGTAA | 6709 |
rs561973288 | snp | C/T | 1.65603e-05 | 0.00287747 | missense | SPTAN1 | GRCh38.p7 | 9:128617750 | TGGCTGCGCATGAGC[C/T]GGCTATTCAGGTAAG | 6709 |
rs562031925 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610332 | GATTTGAACCAAAGG[A/G]TGATCAGAACAAGGA | 6709 |
rs562060048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613230 | CGGGCAGGCTGATTG[A/G]GGTGGCTAGGAATCA | 6709 |
rs562060787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564329 | GAGGCTGAGGCAGGA[A/G]AATTGCTTGAACCCG | 6709 |
rs562073675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625343 | GACTAACTGGGGAAG[C/T]AGACACAGAACCAGG | 6709 |
rs562080368 | snp | C/T | | | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128550651 | ATAGAAAAACCCTCC[C/T]TTTTGAACAGCTCCT | 6709 |
rs562099639 | snp | G/T | | | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128552088 | ACCCTTTGGGACTGG[G/T]CGTTTTTCCGGCCGG | 6709 |
rs562146491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573658 | GACGGGTTTCACCAT[A/G]TTGGCCAGGCTGGTC | 6709 |
rs562153855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606532 | TTTTGTGCCCAGGCT[A/G]GAGTGCAGTGGTGCG | 6709 |
rs562170240 | snp | A/G | 0.000164718 | 0.00907368 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575149 | TTTCTGGAAGCCATT[A/G]TTAACAAATGTTGGT | 6709 |
rs562210218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631008 | GCCACCACATCTGGC[C/T]TAGTTTTTATATTTT | 6709 |
rs562211193 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579969 | CCTACTTACAGGGAC[C/T]TTCTGTAGGGAGCTG | 6709 |
rs562226126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580463 | GTTTTTTAGTATTAC[A/G]TAGAGTAAAGACATT | 6709 |
rs562242266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586892 | GCATGATCTCGGATA[A/G]CTGCAACCTCCACCT | 6709 |
rs562247339 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616164 | TTTTTCTTATTCTCT[A/G]TCTGTCCCCGAAAAT | 6709 |
rs562248463 | in-del | -/AG | 0.0150606 | 0.0854603 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596300 | TTTGTTTTTCGAGAC[-/AG]AGTCTCTCTCTGTTG | 6709 |
rs562263423 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128553155 | TTCTTCCGAATCGCA[C/T]CAGCAATGCCGGCCA | 6709 |
rs562263500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588069 | GTGGCACTATCTTGG[C/T]TCACTGCAACCTCTG | 6709 |
rs562271310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587310 | GGCTGGTCTTGAACT[C/T]CTGGGCTCAAGCTGT | 6709 |
rs562413044 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128552440 | GGCGGTCGGGCGGCG[A/G]GCCGGCGGGAGCACC | 6709 |
rs562432173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631582 | TATAATCCCAGAACT[C/T]TGGGAGGCCAAGACA | 6709 |
rs562433894 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611181 | TACTGCAAGAATTGA[-/T]TTTTTTGGCCAGGCT | 6709 |
rs562514071 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589821 | ACCTCGTGATCCACC[C/T]GCCTCAGCCTCCCAA | 6709 |
rs562573656 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588290 | TATGAGCACTGTGCC[C/T]GGCCCTACTTTAAAA | 6709 |
rs562574544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590390 | GGCTAGTACAACTGG[A/G]TGTTTTATTTAATTA | 6709 |
rs562584290 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619833 | AGTGGTTGAAAGCAG[C/T]ACCCATTTCTTACTT | 6709 |
rs562624725 | snp | C/T | 0.000209358 | 0.0102291 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128627496 | GTGGATCCAAGAGAC[C/T]AGGTGCCAGCCCGCT | 6709 |
rs562644651 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594654 | CCAGACTGGTCTCAA[A/C]CTCCTGACCTCAGGT | 6709 |
rs562649547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595879 | TGAGACAAGGTGTTC[C/T]GTTGCCCAGGCTGGA | 6709 |
rs562706009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595098 | AACAGGCGTAAGCCA[C/T]CGTGCCCGGCCTCAG | 6709 |
rs562771052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560913 | CCCAGCTACTGGGGA[A/G]GCTGAGGCAGGAGAG | 6709 |
rs562824814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575907 | AAGACATCAAGTACT[C/T]GGAACCAGAGAGTTT | 6709 |
rs562834156 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128553320 | TTTCCTTGTAATAAA[C/G]ATTTTTCTTTCTTCC | 6709 |
rs562846988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602672 | TCGGAGTCTTGCTCC[A/G]TTGCCCAGGCTGGAG | 6709 |
rs562875476 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128556133 | AGCTGAGGCAGGAGA[A/C]TCGCTTTAACCGAGG | 6709 |
rs562879010 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633417 | GTGTGCTCTCACTTT[A/C]CACTGTAACCTTAAG | 6709 |
rs562890268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569017 | CTTTTAAAAGAATTT[A/G]TGAAGTCTCCTTAAG | 6709 |
rs562907376 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128633033 | AGAGCTGAGTCTGGG[G/T]TAACAGGCCCTGCGC | 6709 |
rs563056775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607237 | TTGAATTCCTGAGCT[C/T]AAGCGATCCTCCTGC | 6709 |
rs563108421 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609986 | TTGAAGATGGAACAT[C/G]AGCTTCAGCTTTTTC | 6709 |
rs563125604 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623276 | GGTCTCACTATGTTA[G/T]GTTGCCCAGGCTGGT | 6709 |
rs563129888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621934 | CTCAGGTGCAGTGAC[A/G]CACCTGGAGTGCCTC | 6709 |
rs563189066 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617163 | AGGATCACTTGAACC[A/G]GAGTGGCGGAGGTTG | 6709 |
rs563191579 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615459 | CGGTAAAAAATAATA[A/G]TGTCTTATAATGTTA | 6709 |
rs563263700 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603378 | GTATTTTCATGACAT[G/T]CTAGTACTTGACACT | 6709 |
rs563264781 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622759 | TATTTATTTATTTAT[G/T]TATTTATTTTTTAGA | 6709 |
rs563357151 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577784 | GTATCTGAGTATCAC[A/C]TGAAATATCTTATTA | 6709 |
rs563393542 | snp | C/G | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128553719 | CATCTAATCAGATCT[C/G]TTTTATATAATAGAT | 6709 |
rs563422540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563616 | GCAAACTGAAAGATT[C/T]GTTATGGAGCTCTCT | 6709 |
rs563455550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577040 | GTGCTGGTGAGCTGT[C/G]GAGGCTGACTAGGCC | 6709 |
rs563559487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628487 | TCCGCCCTAATAGAA[A/G]GCAAAAATGCACCCG | 6709 |
rs563573561 | in-del | -/ATG | | | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633644 | GTAAAAGACAAATAA[-/ATG]ATGATGACTTCCCCC | 6709 |
rs563650979 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624581 | GCAGAGAAGAAACTG[A/C]TCAATTGTGGGCATG | 6709 |
rs563691394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586975 | GGCGCCCGCCACCAC[A/G]CCCAGCTAACTTTTT | 6709 |
rs563693374 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593810 | CCTCTGTATACATTC[C/T]GCCCAGCAAGTTCAT | 6709 |
rs563717201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618749 | CGGCCTCCCAAAGTG[C/T]TGGGATTGCAGGCAT | 6709 |
rs563719341 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611426 | AGTGAGCTGAGATTA[C/T]GCCACTGCACTCCAG | 6709 |
rs563756462 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587398 | ACCAGGATGAGTAAG[C/G]TATAATCATAATATA | 6709 |
rs563759263 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624065 | TCCAGCCTGGGCGAC[A/G]GAGTGAAATTCACTC | 6709 |
rs563802436 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557825 | TTTTTTTTTTTTGAG[A/G]CGGAGTCTCGCTCTG | 6709 |
rs563831727 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593121 | GCCGCTTCTCTTGAA[C/G]GCCTTTGTCCATCCA | 6709 |
rs563940869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585626 | AATGGAATTATGAAA[A/G]GGCACAGCTCACCAA | 6709 |
rs563948453 | snp | C/T | 0.000347685 | 0.0131803 | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633374 | TCGCTGCTTGCCCTG[C/T]GTCGCCTTGCTGCAT | 6709 |
rs563964306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597524 | GAGACCCCGTCTCCA[A/G]AAAAGACAAAAAACT | 6709 |
rs564024771 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565163 | CAAAAATTAGCTGGG[A/C/T]GTGGTGGTGCAGGCC | 6709 |
rs564135257 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599069 | GCCAAGAACTTCTTC[A/G]TCAGAATTGCTGTTC | 6709 |
rs564136613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559542 | TGTGCAGTGTCGTTA[C/T]TGTTCCATGTGTAAC | 6709 |
rs564155435 | snp | A/T | 1.6473e-05 | 0.00286988 | missense | SPTAN1 | GRCh38.p7 | 9:128598979 | AAGTGTATGGCATGA[A/T]GCCCAGGGTAAGTTT | 6709 |
rs564201202 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599484 | ACAAAAAAAGTTGGT[G/T]TTTTTTTTTTTCGGT | 6709 |
rs564238649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631058 | CCTTGTTGGCCAGGC[C/T]GGTCTGGAACTCCTG | 6709 |
rs564242568 | snp | C/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128552362 | CGCGGCCCGCCCCTC[C/G]CTCACCTCTTCCCCC | 6709 |
rs564248439 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606608 | CCTGCCTCAGCCTCC[C/G]AAGTAGCTGGGATCA | 6709 |
rs564289926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600407 | CCCACCAGTAAGAGG[C/T]GGTCCAAAGGGAAAT | 6709 |
rs564300550 | in-del | -/AAAA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599471 | CATTCTCCAAAAGAC[-/AAAA]AAAGTTGGTTTTTTT | 6709 |
rs564384696 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613980 | ACGGCACTCCAGCCT[A/G]GGCAACAGAGCAAGA | 6709 |
rs564433796 | in-del | -/TT | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633454 | AGCTTGGAATAAGAC[-/TT]TTAGGAGAAAATGGT | 6709 |
rs564462555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619807 | TGCTACATAACAACC[C/T]GCCTAAATGTAGTGG | 6709 |
rs564499693 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621423 | CAAGTTGGATATTTC[C/T]CCCTTTTTGAAGCCA | 6709 |
rs564557794 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567452 | GCCTGCCACTGTGCC[C/T]AGCTAATTTTTGTAT | 6709 |
rs564569351 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128555409 | GTCCAGGTATTTGAC[A/G]AGCATGCAGAAAACG | 6709 |
rs564586129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626292 | CAGCAGGCTGTGTGC[A/G]CCTCTGATTCCCAGG | 6709 |
rs564602973 | snp | A/G | 8.25934e-05 | 0.00642572 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581095 | TGCCAGTGGTGGGAG[A/G]AGAAGGGCCTGTGTT | 6709 |
rs564667478 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573719 | TCAGCCTTCCAAAGT[G/T]CTGGGATTACAGGAG | 6709 |
rs564670933 | snp | G/T | 1.6599e-05 | 0.00288084 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566697 | TTTTCATCTATTTTG[G/T]TGCCTATTGGTACTT | 6709 |
rs564712311 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622612 | CCAGCGAGCCGGCTG[C/G]TTTGTCCTCAGCGAC | 6709 |
rs564725857 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626204 | GACAAGGGCAAAGGG[G/T]AGGAAGGGGAAAAAA | 6709 |
rs564728653 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576707 | TGACCATTATTTCTT[A/C/G]TGATTCTCTTCAGAG | 6709 |
rs564752745 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577658 | ATGTTCTCTCTGTTT[A/G]GAGACTGGCAACTGT | 6709 |
rs564788652 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621587 | AAACATAAAATAAAA[A/G]TTACCCATAAAGCCC | 6709 |
rs564861038 | snp | A/G | 1.6631e-05 | 0.00288362 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615581 | TTCTTATGTTCAAGC[A/G]GATAGCTGTGGGAGA | 6709 |
rs564884135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595659 | CTAGTTCCGAAACAT[C/T]TGTGTCACTTCAGAA | 6709 |
rs564930682 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627660 | GCTCTGGAGCCGGGA[C/G]TGGGGGCATAGGTGG | 6709 |
rs564951495 | snp | C/T | 1.64852e-05 | 0.00287094 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628028 | GCTTGTGGAGGATCC[C/T]GGGATGGGCCTTCCT | 6709 |
rs564955343 | snp | C/T | 1.65143e-05 | 0.00287348 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584892 | CTGCTCCTCGTGTCT[C/T]CCCTTCTTGCCGAGG | 6709 |
rs565012343 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557078 | AGCAACAAAAGCAAC[C/T]GATGAATGGTTTCTA | 6709 |
rs565165102 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569520 | TTTCACATATCTAGT[A/G]TGAAGATATTAAGGG | 6709 |
rs565175857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595253 | TAGCTGGGATTACAG[A/G]TACGCACGACCACAT | 6709 |
rs565176130 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128633121 | TTGTAGAAGCAGCTC[C/T]GAGCCCCCAGCATCC | 6709 |
rs565224976 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596788 | CTCAAACTCCTGTGC[A/T]CAAGTGATCCTCCCA | 6709 |
rs565341958 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629260 | ATCCCCAGGCGGCTC[A/C]ACCCTGACTAACCTG | 6709 |
rs565369914 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606934 | TTGCCCTAGAATAAC[A/G]TTCCTTAACTAATCA | 6709 |
rs565402790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569695 | TTTTCTAGTCTTTTA[C/T]CTGTCAAAGCAGTCC | 6709 |
rs565417733 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128634127 | GAAGCCGTCCTTACC[C/G]CCATGTGTGGTCTTT | 6709 |
rs565450433 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602213 | TTTGTTTTTTTTGGG[G/T]TTTTTTTGTTTTTTT | 6709 |
rs565472246 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573772 | TTCTACTTTTTTTTT[C/G]AGACGGAGTCTCGCT | 6709 |
rs565503203 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591313 | CCTCGTAATCCACCC[A/G]CCTCGGTCTCCCAAA | 6709 |
rs565514244 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603050 | CTTTATTTTTTCCCT[C/G]TGGTAAAGCCGTTGC | 6709 |
rs565590476 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | SPTAN1 | GRCh38.p7 | 9:128608172 | GAGAACTGGATGGCT[A/G]CCCGGGAGGCCTTCT | 6709 |
rs565706107 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585204 | ATTTTTATTTTTGTA[G/T]TTTTAATAGAGACAG | 6709 |
rs565783033 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590773 | GGGGAATCACTTAAA[C/T]CCAGGAGGCAGAGGT | 6709 |
rs565816663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570091 | ATACAGTCTTAGAGT[A/G]AATGAAATCAGTCTG | 6709 |
rs565854328 | snp | C/G | | | downstream-variant-500B, missense | SPTAN1, WDR34 | GRCh38.p7 | 9:128633873 | AGCCAAGAGCTGAGT[C/G]TGCTGGCTGTTGAAC | 6709 |
rs565877313 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558159 | CCACTCTTCTTCCGA[G/T]ATCTGGTAGTATTGT | 6709 |
rs565885424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128556672 | CCTCTGCAAAATTGC[A/G]CTAACAAGTTGAAAT | 6709 |
rs565918853 | snp | A/T | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128553902 | AAAACAGAATGTATC[A/T]AAGATGGAAGGGTGG | 6709 |
rs565979192 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582443 | AGCTTGGGACTAGTG[G/T]GCTTACCAATGAAGA | 6709 |
rs565989180 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598256 | CCCCCAGCCATAGCT[G/T]ATTTTTTTAATCCCC | 6709 |
rs566021791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562960 | ACAGAGTGAGACTCC[A/G]TCTAAAAAAAAATAT | 6709 |
rs566054817 | snp | C/T | 3.29582e-05 | 0.00405931 | missense | SPTAN1 | GRCh38.p7 | 9:128605101 | ACAGACAATTATGGA[C/T]ATGATCTCGCCAGTG | 6709 |
rs566084355 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581127 | TGCCTCCTCGGGTAG[G/T]GTGCTTGTTTTGTTT | 6709 |
rs566103184 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589495 | GGGTTTCACCGTGGT[C/G]TCTATCTCCTGACCT | 6709 |
rs566117604 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558361 | AATATTTTGCAAATA[C/T]ATACCTTTTTTTTTA | 6709 |
rs566117672 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618412 | GACATGAGAGTCTGG[A/C]ATCACAGAGTGGGTG | 6709 |
rs566132111 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610758 | ATCCTTCTCCTAGCC[C/G]TTTCATTTCCCAGTA | 6709 |
rs566144228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572204 | CATTCCTGTCTTCTT[C/T]GCTTAATGTTTCCAC | 6709 |
rs566173681 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610918 | AGAGGGAAAAGACTG[A/T]CCATCAAATATTATT | 6709 |
rs566191396 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611465 | ACTGAGCAAGACCCT[A/G]TCTCAAAAAAAAGGA | 6709 |
rs566226873 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580796 | GTTGTTTTTCCCCTT[C/G/T]TGCAAATCGGAAAAA | 6709 |
rs566269345 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624166 | GTGAAGCCTTTGACC[A/G/T]CATTGCTCTTACAAA | 6709 |
rs566298255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573389 | TGTCTTTTCACAGAA[A/G]GTCCAAAGTTTTTTC | 6709 |
rs566304729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586617 | TACCTACAAACATAC[C/T]AGCATACACATGTAC | 6709 |
rs566326562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623575 | GTTCTCATCCCTCAG[C/T]CTCCTGGGTCACTGG | 6709 |
rs566366732 | snp | C/G | 1.66399e-05 | 0.00288438 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585697 | TATTTTTGTCCTTCT[C/G]TGATGTGTCAACGTA | 6709 |
rs566387921 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617498 | CATTTGGGAAGTAGA[C/G]GCTTTTGTTGTTCAG | 6709 |
rs566396366 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128550710 | CTGGAGCAGAAGGTC[C/T]TGGAAATTTTAGGGA | 6709 |
rs566457818 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128551780 | AGCTTTTGTTGCAGG[A/T]ATGTAAGAAATTATT | 6709 |
rs566479163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573776 | ACTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 6709 |
rs566516976 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576032 | TAAGAGAAAGATACC[C/T]GGCATTCCTCAGAAA | 6709 |
rs566548909 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559786 | GTCGCCCAGGCTAGA[A/G]TGCAGTGGTGCGATC | 6709 |
rs566633513 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593203 | ACAAGGGAAGAGGTC[A/G]CGGTGCAGCTGTGTC | 6709 |
rs566665608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592763 | AAGCATGGCAGACCC[A/G]CCAGGAAAATGAAGG | 6709 |
rs566672621 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631224 | GCACTTTGGGAAGCC[A/G]AGGCGGGTGGATTGC | 6709 |
rs566701114 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606658 | CCGGCTAATTTTGTA[G/T]TTTTTTTAGTAGAGG | 6709 |
rs566708764 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599961 | AAAATGCTGTTTTGG[C/T]TAATGTATTAGTATC | 6709 |
rs566735758 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601589 | TGTTTTAAAAAGAAG[A/G]AGAAAAAAAGTAGGC | 6709 |
rs566771857 | snp | C/T | 6.59772e-05 | 0.00574319 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599056 | GGAAGAATATCAAGC[C/T]AAGAACTTCTTCATC | 6709 |
rs566772447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600633 | GAATGGGCCATCCCT[A/G]ACCAAGAATACAGGG | 6709 |
rs566907855 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582159 | AATATTAAGAGGTAC[G/T]CTTCCCATTGAAAAT | 6709 |
rs566938344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128553784 | CATGTTATTTTAGAA[A/G]AACTTACCATCATGG | 6709 |
rs567000546 | snp | C/T | 0.000399281 | 0.0141238 | missense | SPTAN1 | GRCh38.p7 | 9:128594258 | TGTTGTTCCGTGAAG[C/T]GAATGAACTACAGCA | 6709 |
rs567066075 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554768 | GAGGACTGCATAGCT[C/T]ATCACTGGGGGCCAC | 6709 |
rs567074262 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602886 | GGTGATCCACCCACT[G/T]TGGTCCCCCAAAGTG | 6709 |
rs567075126 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128552742 | GGAGCGGGGCCCCGG[A/G]CAGCCGACCCCCGGG | 6709 |
rs567076921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561110 | CACGGTGGTTCACGC[C/T]TGTAATCCCAGCACT | 6709 |
rs567092577 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594891 | TGGAGTGCAATGGTG[C/T]GATCTCGGCTCACTG | 6709 |
rs567106525 | snp | C/G | 1.69424e-05 | 0.00291048 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613527 | CGAGTGCCTGGGACA[C/G]AGCTCTGCCTGACTC | 6709 |
rs567133281 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567062 | AGGAAAGTTACTTAA[A/T]TATGACCTTGAGAGA | 6709 |
rs567160596 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602824 | TATTTTTAGTGGAGA[C/T]GGGGTTTCACCATGT | 6709 |
rs567164772 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623236 | TAATTTCTTTCTTTT[C/T]TTCTTTTTTTTTTTT | 6709 |
rs567191510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627725 | AGTTGTTAGAGATCC[C/T]GGATTGAGTGGGACC | 6709 |
rs567205255 | snp | A/G | 1.64773e-05 | 0.00287026 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128615739 | CAACGGGCGCTTCCA[A/G]AAGATCAAGAGCATG | 6709 |
rs567214619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560466 | GCTCACTGCAAACTC[C/T]GCCTCCCAGGCTCAA | 6709 |
rs567249249 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602313 | CCTCTGCCTCCTGGG[G/T]TCAAGCAATTCTCCC | 6709 |
rs567283571 | snp | C/T | 6.59033e-05 | 0.00573997 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578073 | CCACCCTGGAACCTC[C/T]GCTGGAAACATAATG | 6709 |
rs567295117 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562215 | TCAAGCGATTCTTCT[C/G]CCTCAGCCTCCCGAG | 6709 |
rs567336345 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561761 | TATTCTGGGAACCGG[A/C]GGATCCCAGGTCATC | 6709 |
rs567343417 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570921 | CCGCCTTGGCCTCCC[A/G]AAGTGCTGCGATTAC | 6709 |
rs567370036 | snp | C/T | 3.31373e-05 | 0.00407032 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566714 | GCCTATTGGTACTTA[C/T]CTCAGCGCATTTTGT | 6709 |
rs567417206 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621095 | GTCACTCTCTGTCCC[A/C]GGGGCCTAGCCCACA | 6709 |
rs567426858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575531 | TGGAAAATGCTTTTC[A/G]ATGTGTTGCCTTGGG | 6709 |
rs567446498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614915 | GCAACATCATGCATG[A/G]CTCATTTGGTAAATA | 6709 |
rs567546193 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617382 | CTCAGGGCAGCACTA[G/T]TGATGCCTCCCATCC | 6709 |
rs567607738 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570269 | AAGCTGACTTTATTC[A/C]TGTCTATTAGTACCC | 6709 |
rs567671139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563144 | AAAATAGGCCAGTGC[A/G]GTGGCTCATGCTTGT | 6709 |
rs567730112 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622910 | GGCGCCTGCCACCAC[A/G]CCCAGCTAATTTTTG | 6709 |
rs567765056 | snp | C/T | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128553752 | TAAAATATTTAAGCC[C/T]TTTGTTCTGTCTTCA | 6709 |
rs567896938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597082 | TGAAGATCGCTTGAA[C/T]CCGGGAGGCGGAGGT | 6709 |
rs567903460 | snp | A/G | 1.70898e-05 | 0.00292311 | downstream-variant-500B, synonymous-codon | SPTAN1, WDR34 | GRCh38.p7 | 9:128633939 | CTTGATCAAAACTGT[A/G]GGTTTCTGGGAGCTT | 6709 |
rs567925858 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633555 | AGCAGCTGCCCTCAT[C/T]CCGACTTCAGAAAAT | 6709 |
rs567933253 | snp | A/G | 0.000399281 | 0.0141238 | missense | SPTAN1 | GRCh38.p7 | 9:128585960 | AAGGACGAAGACTCT[A/G]CTGAGGTAACCAGGC | 6709 |
rs567949333 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585640 | AGGGCACAGCTCACC[A/G]AAACATAGTAATGAA | 6709 |
rs567960292 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597763 | TCAAGCGATTCTCCT[C/G]CCTCAACCTCCCGAA | 6709 |
rs567969348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596478 | AGATGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 6709 |
rs567999992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628278 | GCCTGTCCAGCCACC[A/G]GGCTCTGTTGGGCTC | 6709 |
rs568094941 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578810 | CTCCCGTCCGGACAA[C/T]AAGAGTGTTTCACTC | 6709 |
rs568122669 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128551877 | AGAATGACAGCTTTA[C/T]GCCCCAAATTAGTCG | 6709 |
rs568178078 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595260 | GATTACAGGTACGCA[C/T]GACCACATCTGGCAA | 6709 |
rs568196549 | in-del | -/TGTC | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625024 | ACACAAAAAATGGTT[-/TGTC]TGGGTTTTGATGTTT | 6709 |
rs568218179 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609541 | CTATTACTGTTCCCA[A/T]ATGCTGAGCTTCCTG | 6709 |
rs568248781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563789 | AGTGTGACTACGGGC[A/G]CATGCCACCATGCCT | 6709 |
rs568261872 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128551021 | TCAGTATCATGGCTA[C/T]AGCCAGGACAGCTTA | 6709 |
rs568307655 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557517 | CTGTACAAGAAGATA[C/G]AGCTATATATCCCAT | 6709 |
rs568373026 | snp | A/C | 0.000313203 | 0.0125101 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617949 | CAGAAGCACCAGAAG[A/C]GCTACCTGCTGTTAA | 6709 |
rs568381051 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624718 | ACAAAAGCCTGTAAA[C/T]GCTGCTGCACGCAGA | 6709 |
rs568418347 | snp | A/C | 1.64887e-05 | 0.00287125 | missense | SPTAN1 | GRCh38.p7 | 9:128605390 | CAGAGTTAAACCAGG[A/C]CTGGAGCAGCCTGGG | 6709 |
rs568476470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567125 | ACTCATTGTTTTCCT[C/G]TATTAGTGAGGGTGA | 6709 |
rs568496894 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612400 | TTGCATGCTGTAAGG[A/G]ATTTATGAGCAAAGG | 6709 |
rs568553002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611523 | TACATTTCCTTCCTC[C/T]TTTGCTAACTCCCCA | 6709 |
rs568581000 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565287 | GCCTGGTGACTGAGC[A/G]AGACTCCGTCTCAAA | 6709 |
rs568586720 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559787 | TCGCCCAGGCTAGAG[C/T]GCAGTGGTGCGATCT | 6709 |
rs568678002 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616082 | TGCCTTTTAGATTCC[C/T]GTGAAAGTTAGTGAG | 6709 |
rs568743023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606414 | TCTACTTTCCTATCC[A/G]AGTATGGGCATACTC | 6709 |
rs568770416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571648 | GTTTGTTGAGTAGGT[A/G]TTAGGAGCTATTTAT | 6709 |
rs568783589 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560533 | CTACAGGCATGTGCC[A/C]CCACACCCAGCTAAT | 6709 |
rs568791402 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561083 | CCATCAATAAATAAT[A/G]TGTCGGCCAGGCACG | 6709 |
rs568817946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614198 | AGTGGCTCACACCTG[C/T]AATCCCAGCACTTTG | 6709 |
rs568821010 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604820 | CCTGTAATCCTAGCT[A/T]CTTGGGAGGTTGAGG | 6709 |
rs568877997 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613610 | CAGCCATTCTCAAAG[A/G]TTGTGGCCTCAGGAT | 6709 |
rs568882666 | in-del | -/ATT | 0.00517822 | 0.0506191 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557031 | CCACGGAAAAAAGAC[-/ATT]GTTGGTTCTGCACAT | 6709 |
rs568906829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621778 | CATTTTAGAAATGAA[C/T]CTACTTCATTCGCAG | 6709 |
rs568930393 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580868 | CTGTTCTGTCTGCCT[C/T]GGAGGCATTGGGGCT | 6709 |
rs568931979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620011 | CCCTCCACATGGCCT[A/G]TTGTCCTCAAGCTGG | 6709 |
rs569030288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631329 | CTGGGTGTGGTGGCA[A/G]GCACCTGTAATCCCA | 6709 |
rs569065100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587125 | CGCGCTCGTTCTGTC[A/G]CTAGGGCTGGAGTAC | 6709 |
rs569077485 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594903 | GTGCGATCTCGGCTC[A/G]CTGCAACTCCTCCTC | 6709 |
rs569153259 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595323 | CCATGTTGGCCAGCC[G/T]GGTCTTGAACTCCTG | 6709 |
rs569156901 | snp | G/T | 0.000238819 | 0.0109249 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628093 | CTCGTCACCTGATGA[G/T]GAGTGTGTGCCTTGC | 6709 |
rs569168004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631873 | TCCTCGCCGTACTTG[C/T]CCTTGGCGTGCACTG | 6709 |
rs569190941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583628 | ACCTTGAGAAGGTAG[A/G]GCAGAGGCTGCAATT | 6709 |
rs569205795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583012 | AAGATAAGTATGAAG[A/G]TAGTGCAAGGGAACT | 6709 |
rs569214868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600761 | TCCGCCTCCCCAGTT[C/T]GAGCAATTCTCCTGC | 6709 |
rs569240602 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599942 | CCAGCCAAACTATGG[-/A]GGGAAAATGCTGTTT | 6709 |
rs569309089 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575592 | CCTCTACCCACTTTT[C/G]GGTAGGGCTGGGTGA | 6709 |
rs569317594 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128634070 | CCCGGGTTCAATCCT[G/T]TTGTGTGCAGCCACA | 6709 |
rs569353227 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625384 | GCAGCCTGCTGGGTG[C/T]TGACGGGACTGGGCA | 6709 |
rs569358182 | snp | C/T | 0.000197977 | 0.00994733 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632559 | CTGAGCCGCCCTCGG[C/T]TTTGTGCTGCAGACA | 6709 |
rs569371380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627750 | GGGACCATGCAGGGC[A/G]CGTGGTCAGCCCCAG | 6709 |
rs569380220 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588700 | AGAATTCTCATGAGT[A/G]TATATTTGGTACATT | 6709 |
rs569571884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622199 | CTCCTGCACACTTAA[C/T]CCCCTGACACACACC | 6709 |
rs569659031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603007 | ATGTACGTTGTTGAA[A/G]TGTACGTTGTTGAAA | 6709 |
rs569674959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571507 | GGAGAATTGCTTGAA[C/T]TCAGGAGGCGGAGGT | 6709 |
rs569718670 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128555768 | AGAACCAAGGGACTA[A/C]ACATATTATCCTAGA | 6709 |
rs569791769 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570948 | TTACAGGCATGAGCC[A/G]CCGCTCCTGGCCTAG | 6709 |
rs569795061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608695 | CTACTCTAGTAATGA[A/G]TGAAATCAAGCTTTC | 6709 |
rs569854825 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563933 | GTGAGCCATGGCGCC[C/T]GGCCTATTCAACCAA | 6709 |
rs569877920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602405 | TATTTTTAGTAGAGA[C/T]GGGGTTTCGCCAAGT | 6709 |
rs569997507 | snp | C/T | 5.34107e-05 | 0.00516745 | missense | SPTAN1 | GRCh38.p7 | 9:128604371 | CAGCTGGCCGAGGAA[C/T]GGAGCCAGCTCTTGG | 6709 |
rs570017499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603709 | GACATATCTCACTCT[A/G]TTGGGTCCAAGCATG | 6709 |
rs570022109 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623006 | TCCGCCTGCCTCGGC[C/T]TCCCAAAGTGCTGGG | 6709 |
rs570033690 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557588 | TTATGCCCCCAAATA[C/G]CCCCAAATTTTTATT | 6709 |
rs570104855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585078 | GGAGTGCAGTGGCGC[A/G]GTCTCAGCTCAGTGG | 6709 |
rs570111238 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618673 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTCT | 6709 |
rs570126068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617434 | CAGAATCCGGACACA[C/T]AGCAGGGCTCATAGA | 6709 |
rs570170415 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617263 | AAAAGTGTGTATATA[G/T]GTATATATATAAATA | 6709 |
rs570171059 | snp | A/G | 3.29495e-05 | 0.00405877 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128578116 | TTTCCCTAGGCTTCA[A/G]CGCTTCCTTGCTGAC | 6709 |
rs570184267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617824 | CCCAGGGGACAGACA[A/G]ACCCCTTGCGCTTAT | 6709 |
rs570186441 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609598 | ATTTAATAGCTGATA[C/T]GTGTGTCCACATCAG | 6709 |
rs570206241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586485 | TAAAGGAGAGAGAAG[A/G]TGACTTCTCACTCAC | 6709 |
rs570245370 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589351 | TAGAGTGCAGTGGCA[C/T]GATTTCAGCTCACTG | 6709 |
rs570247500 | snp | C/T | 0.000857746 | 0.0206915 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128608933 | CGCTGCCGGCCATTA[C/T]GCCAAGGGAGACATT | 6709 |
rs570263778 | in-del | -/ATATATATA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570322 | TATATATATATATAT[-/ATATATATA]TTTTTTTTTTTTTTT | 6709 |
rs570278215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591894 | TTTGCCTTTTGGTTC[A/G]AGATGCTTTTTGAAA | 6709 |
rs570286951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629117 | TTTGGTTTCTTTTCT[C/T]TGAATAGCATAGCAT | 6709 |
rs570299569 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628726 | CAAGCCTGTATAGGC[A/G]GCCAGGGGAGAAATA | 6709 |
rs570308267 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557826 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 6709 |
rs570308532 | snp | A/G | 1.70866e-05 | 0.00292284 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579586 | CAGCACCTTGTTTTT[A/G]TTTTGTAAGATGCTG | 6709 |
rs570322773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560138 | GCCCAGGCTGGAGTG[C/T]AAAGGCGTGATCTTG | 6709 |
rs570341745 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592656 | ATTGCCTGTTAGCAC[G/T]CAGTAAAATTTCTTT | 6709 |
rs570342041 | snp | A/G/T | 0.00138198 | 0.026251 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586013 | GGGAAGTGGAACAGG[A/G/T]CTTGTACTGAGAAGG | 6709 |
rs570356219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591264 | GTAGAGACGGGGTTT[C/T]ACTGTGTTGGCCAGG | 6709 |
rs570363044 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623095 | AGTCTTGCTCTTGTC[A/G]CCCAGGCTGGAGTGT | 6709 |
rs570366035 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572514 | AAATATGTGAGATGG[A/G]CAATTGACTTGAATG | 6709 |
rs570426240 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625529 | CTGGGCAGAGCTGGC[A/G]GGGATCCCTGGGGCG | 6709 |
rs570516394 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631946 | AAAGTCTCTCCCTCT[A/G]TTGAGGTGGTTGGGA | 6709 |
rs570593613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598190 | CGACCTCAGGTGATC[C/T]GCCCACTTGGGCCTC | 6709 |
rs570634710 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630070 | CATCCTGGCCTTGGG[A/C]GCAAGACGAGTGGGC | 6709 |
rs570658699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597860 | TTCACCATATTGGCC[C/T]GGCTGGTCTTGGACT | 6709 |
rs570772614 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619196 | CTTCAGTAAACAAAA[C/T]TGGTATGGCTTTGTC | 6709 |
rs570821078 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128552104 | CGTTTTTCCGGCCGG[A/G]GCGCGCAGCATCCCC | 6709 |
rs570824675 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594112 | TCGTGGTTTGCCTTT[A/G]TGTTAGCATCTACAG | 6709 |
rs570832082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612560 | TTAGAAACCAAGATA[A/G]TAGCATCTGGGAAGC | 6709 |
rs570885419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587772 | TCAGCAGGTGTTCCT[A/G]TCATAGGCCCCATTT | 6709 |
rs570912876 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561755 | GTGCCATATTCTGGG[A/T]ACCGGAGGATCCCAG | 6709 |
rs570922185 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560315 | TCTCGAACTCCTGAG[C/G]TAAGGCAATCCACCC | 6709 |
rs570927856 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599908 | CTTAATTTTTCTTAA[C/G]CAGCCTTGTAGTTTG | 6709 |
rs570950377 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | SPTAN1 | GRCh38.p7 | 9:128552623 | AACGGTGTGGAGCGG[A/G]GGCCGCGGAGGCTCC | 6709 |
rs570986219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567909 | GGGAATGTAGGCACG[C/T]GACACCACGCCCAGC | 6709 |
rs570996919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599202 | TGCAGTGGTGTGATC[C/T]TGGCTCACTGCAACC | 6709 |
rs571036778 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619838 | TTGAAAGCAGCACCC[A/T]TTTCTTACTTCCAAT | 6709 |
rs571056774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559883 | GGGACTACAGGCGTG[C/T]GCCACTATGCTTGGC | 6709 |
rs571069538 | snp | A/C | 0.00222289 | 0.0332642 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627108 | GTGAGCCACTGTACC[A/C]AGCCAGAAGTTTCCA | 6709 |
rs571073374 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606109 | GGGCACGGTGGCTCA[A/C]GCCTGTAATCCCAGC | 6709 |
rs571135782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565331 | AAAGCCATAAAAGAT[C/T]TGGGAGTGGCATGGC | 6709 |
rs571145675 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563017 | ATATATATATATATA[C/T]ATATATATATGTATA | 6709 |
rs571201891 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565950 | TTGAGGCATGGAGAG[A/G]GAAGGTGGCTAGTGT | 6709 |
rs571230679 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596895 | CCGGGCCCAGTGGCG[A/C]ATGCCTGTAATCCCA | 6709 |
rs571249823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607332 | TCATTTGAAGCTATC[A/G]AAGACTTAATTGTAG | 6709 |
rs571298225 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616099 | TGAAAGTTAGTGAGT[C/T]TGTTTCTGAGCTTCT | 6709 |
rs571368691 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128553789 | ATTTTAGAAAAACTT[-/A]ACCATCATGGCTGTT | 6709 |
rs571389510 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614886 | GAATGTAGCTCTTAC[A/C]TGTGCATGATTTTGC | 6709 |
rs571417223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621009 | ATTCTCTATTTATTA[A/G]TGTTCCTCTTTATTA | 6709 |
rs571433254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574606 | TCTAACTTGTCTAAA[C/T]TCTATGGAAGAGCCA | 6709 |
rs571439823 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581718 | CAAAATACCCTTTGC[C/T]TCACAGTCTTAGAAG | 6709 |
rs571451003 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602659 | ATTTATTTTCGAGTC[A/G]GAGTCTTGCTCCGTT | 6709 |
rs571473649 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589424 | CTCCCGAGTAGCTGG[G/T]ACTACAGGCGCCCAC | 6709 |
rs571478742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620256 | GTGTGCACTCCCAGG[A/G]ATCGAGTTAGCTTTG | 6709 |
rs571524862 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573369 | ACTTGAGATGTACCA[C/T]AAACTGTCTTTTCAC | 6709 |
rs571529341 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613833 | ACGTGGTGAGACCTC[C/T]GTCTCTACTAAAAAT | 6709 |
rs571532516 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589875 | CCACCGCGCCTGGCC[C/G]ACCTGTTGGTTCTTA | 6709 |
rs571532593 | snp | C/T | 1.66023e-05 | 0.00288113 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583074 | CCCTTCTTTTATTCA[C/T]AGGATCCATCCAACC | 6709 |
rs571542017 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622791 | GGAGTCTCACTCTGT[C/G]GCCCAGGCTGGAGTG | 6709 |
rs571551626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626976 | CGTGCCACCACGCCT[A/G]GCTAATTATTTTAAT | 6709 |
rs571572081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576414 | AAAGCCAGGGACAAA[C/T]TCTTGAGCCCCGAAA | 6709 |
rs571606934 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563822 | ATAATTTTTTTTTTA[A/G]AGCCAGGGTTTAGCC | 6709 |
rs571634122 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569457 | GTCTGGCTGATTTTA[G/T]TGCGAGTTTATTGGA | 6709 |
rs571634565 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128555469 | AGTGAAGGCATATTC[C/G]TGTCAAAGAGGTTGA | 6709 |
rs571656803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561145 | GAGGCCGAGGCGGGC[A/G]GACCACAAGGTCGAG | 6709 |
rs571714900 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596001 | GGTATGCACCACTAT[C/G]CTCAGCTAATTTTTG | 6709 |
rs571739945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622321 | TTTTTTTTTTTGCGA[C/T]GGAGTTTCGCTCTTG | 6709 |
rs571752722 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627773 | AGCCCCAGCCATGAC[G/T]TGGTGACAGACGATG | 6709 |
rs571852822 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628755 | TAGACCCATCCAGCC[G/T]GGCCACACATTCTGA | 6709 |
rs571859220 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633349 | AGCCACTCCCTGGGT[C/T]ACCCACCCCTCGCTG | 6709 |
rs571874466 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554597 | ATGGACAAGTGTGTT[C/G]AAGGCTGGCCTGCCT | 6709 |
rs571946563 | snp | A/C | 0.0391387 | 0.134304 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623178 | CTCCCACCTGAGCTT[A/C]CCTAGCTAGCTGGGA | 6709 |
rs572012067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616488 | AAAGACGTTTGTGGC[C/T]GGGCGCAGTGGCTCA | 6709 |
rs572014219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128633122 | TGTAGAAGCAGCTCC[A/G]AGCCCCCAGCATCCT | 6709 |
rs572024054 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590793 | GAGGCAGAGGTTGCA[A/G]TGAGCCAAGATCGTG | 6709 |
rs572040089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569760 | CAGCTAGAACTGTTT[C/T]GTCTCCTACTCTTCC | 6709 |
rs572134185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596267 | TTTTTTGTTTTGTTC[A/G]TTTTTTTTGTTTGTT | 6709 |
rs572149560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622624 | CTGCTTTGTCCTCAG[C/T]GACAGCCTGTTTCCT | 6709 |
rs572157016 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585488 | TGTTACTAGTCTTTA[A/T]GATACTATCACTAAT | 6709 |
rs572181991 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584087 | ATGTGTTGATTTTCT[G/T]AGATCGCTCTGTGCT | 6709 |
rs572195712 | in-del | -/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594827 | TTTTTTTTTTTTCAA[-/T]TTTTTTTTTTTTCCT | 6709 |
rs572254140 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589686 | GTTCACGCCATTCTC[C/G]TGCCTCAGCCTCCCG | 6709 |
rs572259819 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563331 | TGAGGCGGGAGGATC[A/G]CTGGAGCCCAGGAGG | 6709 |
rs572264560 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602459 | TAACCTCACCTGATC[C/T]ACCCGCCTTGGCCTC | 6709 |
rs572323435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557110 | GATCTTTTGCTTTGG[A/G]TGATGTTTATGAATT | 6709 |
rs572325963 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587291 | GGTTTCAGTATGTTG[C/T]CCAGGCTGGTCTTGA | 6709 |
rs572410813 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128555811 | ATAATCTGAAAATAC[A/T]TAGTAAAAATTGTGT | 6709 |
rs572453314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592057 | TCTAGCTGAGCCCCC[A/G]TATTGCCCTGTGTCC | 6709 |
rs572471199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597366 | AAAAGTCTCTATTTG[A/G]TAAAATTATTTGCTG | 6709 |
rs572487840 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629554 | CCCACCAAGGCCACA[C/G]GCACCGTGTGATTCG | 6709 |
rs572524876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603819 | AGTGGAGCAAGCCTT[C/T]CCTCTGATTTCCAGT | 6709 |
rs572614457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616972 | GCTGGGTGTGGTGGC[C/T]CACGCCTATAATCCC | 6709 |
rs572632348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604854 | GAGAATCACTTGAAC[C/T]CGGTGGGGGCGGAGG | 6709 |
rs572667316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609728 | TTTGTGTTACTCTGC[A/G]TAGATTATTGTTATT | 6709 |
rs572675082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579102 | AGTACACAGATGGAA[C/T]GATCTTCTGTGAAGG | 6709 |
rs572736018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579840 | GAGAACGCATTCACC[A/G]TGATATGTGAGAAAC | 6709 |
rs572776196 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571794 | GTCACACAGTTGATA[A/G]ATGACTGAACTGGAA | 6709 |
rs572803488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609036 | ATGCATCCCCTCATA[C/T]GAAGGCCCAGGCCTG | 6709 |
rs572811873 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586122 | ACTTGGTTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 6709 |
rs572812215 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578490 | CAGACAAGCTCTGGC[A/G]AGATAGAAGTGCTAC | 6709 |
rs572832203 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558530 | TTGATTGCATTCCTA[C/G]GAAGTCGTCTCTGTT | 6709 |
rs572841021 | in-del | -/TAAA | 0.00795532 | 0.062565 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604934 | GAAACTCCATCTCAG[-/TAAA]TAAATAAATAAATAA | 6709 |
rs572863471 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618704 | TAGCCAGGATGGTCT[C/T]GATCTCCTGATCTCG | 6709 |
rs572890447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572590 | GCAGGAGCTCTCATT[C/T]AATCTTTTACTTTCA | 6709 |
rs572958583 | snp | A/G | 0.000148609 | 0.00861873 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128618052 | AGAGGAGATCCAGCA[A/G]CGGCTGGCGCAGTTT | 6709 |
rs572980957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626149 | GCAAATGAGAGGGCC[C/T]TGTGAGATCGCCATT | 6709 |
rs572986011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571977 | TTCACCCACCTCAGC[C/T]TCCCGAGTAGCCGGC | 6709 |
rs573017269 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570930 | CCTCCCAAAGTGCTG[C/T]GATTACAGGCATGAG | 6709 |
rs573080395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624866 | GGGGTCCACGTGTCC[C/T]GGGTAGTAGTAATAG | 6709 |
rs573105285 | snp | G/T | 0 | 0 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601210 | CTGGTCTCAAACTCC[G/T]GACCTCGGGTGATCC | 6709 |
rs573109975 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562316 | CCATGTTGGCCAGGC[A/T]GGTCTGGAGCTCATG | 6709 |
rs573117012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631501 | TACACCTGCTCAAAG[C/T]CCAGCATGGGCAATA | 6709 |
rs573132440 | in-del | -/TT | 0.209693 | 0.246729 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557800 | TAAATTAGAAATTTC[-/TT]TTTTTTTTTTTTTTT | 6709 |
rs573150948 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630124 | AGCAGCTTCCCATCT[C/G]TAAAACGGGAGAAAT | 6709 |
rs573161912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613204 | GACCGAGTGGAGAGA[A/G]TGTCTCAGGCCGGGC | 6709 |
rs573169501 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603408 | TTGTACTGATGTCTC[C/T]GTTAAGAATGTTGAC | 6709 |
rs573218149 | snp | C/T | 8.82745e-05 | 0.006643 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624531 | GCCTTCCCAGAGCTG[C/T]TCTTTGTCTCCTTCC | 6709 |
rs573370991 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593606 | GAATGGCACAGATAC[A/T]CAGTACTGTGCCTGA | 6709 |
rs573384428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554091 | AATGTGCTGCGGAGG[A/G]AAAAAAAAGTGCTGC | 6709 |
rs573432554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587231 | CTTGGACTACAGGCA[C/T]GCACCATCACATCTG | 6709 |
rs573458217 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586806 | AAAAACTAGAATGAG[A/T]TGAATTTTTCCTTTT | 6709 |
rs573520889 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128553244 | TTAATTTCATCCTGC[A/C]TGGCGAATCTCTGCC | 6709 |
rs573539800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595536 | AACTACAATAGATGT[A/G]AAAGTACTCTTTTTT | 6709 |
rs573558478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559990 | TCCACCCGCCTTGGC[C/T]TCCCAAAGTGCTGGG | 6709 |
rs573558759 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128551237 | CTGACTGCACAGGAA[C/T]GATCTGGGTGTTACT | 6709 |
rs573559899 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600872 | TTCGCCATGTTGGCC[A/G]GGGTGGTCTTTAACT | 6709 |
rs573564088 | snp | A/G | 1.66228e-05 | 0.0028829 | missense | SPTAN1 | GRCh38.p7 | 9:128588929 | ATCCTTACCTTACTC[A/G]ACAGCACCAACAAGG | 6709 |
rs573623459 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128552266 | GTGAGGCGGGAGCGT[C/G]TCTACCGCCAGGGCG | 6709 |
rs573630377 | in-del | -/ATTT | 0.0107246 | 0.0724382 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587838 | AGAGTTTAAAATAAG[-/ATTT]ATTTATTTATTTATT | 6709 |
rs573702134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595065 | TCCGCCTGCCTCAGC[C/T]TCCCAAAGTACTGGG | 6709 |
rs573739962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560890 | GTGTGGTGGCGGGTG[C/T]CTGTAATCCCAGCTA | 6709 |
rs573848432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613801 | CTGAGGTCAGGAGTT[C/T]GAGACCACTCCGGCC | 6709 |
rs573871245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575783 | ACCTTGTCGTGAATA[A/G]GCTCTCCACTCTGGC | 6709 |
rs573880731 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614464 | GGGCGTGGCATGTGC[C/G]TATAAATCCCGGCTA | 6709 |
rs573907913 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605734 | CAGTGGCTCACGTCT[A/G]TAACCCCAGCACTTT | 6709 |
rs574014330 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606499 | TATATTTTTTTTTTG[G/T]GGGGGGAAGCGTTTC | 6709 |
rs574017017 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616210 | CCAGTTGATGTGGCA[C/G]GTAAACAAACATTTT | 6709 |
rs574080395 | snp | A/G | 8.26535e-05 | 0.00642806 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608298 | CCTCTGGACCATGGA[A/G]TTGGAGTCTGGATTT | 6709 |
rs574164340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623212 | CAGGTGGGTGTCAAC[A/G]CACCTGGCTAATTTC | 6709 |
rs574171577 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617548 | CCAGAAAGATTAGTA[A/G]ATGTCTGTGAGGTCC | 6709 |
rs574181722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631226 | ACTTTGGGAAGCCGA[A/G]GCGGGTGGATTGCTT | 6709 |
rs574212968 | snp | A/G | 3.29647e-05 | 0.00405971 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568923 | GTAGCTCGTGGAGTG[A/G]ATGGCTTCATCTGGG | 6709 |
rs574226287 | snp | C/T | 0 | 0 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623731 | TGCCCACCTCAGCCT[C/T]CCAGAGTGCTAGGAT | 6709 |
rs574288711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622518 | TGGTCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 6709 |
rs574349039 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596303 | GTTTTTCGAGACAGA[A/G]TCTCTCTCTGTTGCC | 6709 |
rs574420086 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621907 | CGTGGGTCGGGAATT[C/T]ACCAGCAATCACTCA | 6709 |
rs574448108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629303 | GCTTGGGAAGGAGGG[A/G]TCTGTCCTCCCACTG | 6709 |
rs574458883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570631 | GCTTGAGCCACCGTG[C/T]CCAGCCCAGATGGCT | 6709 |
rs574506181 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617039 | ATCCAAGAGTTTGAG[A/T]CCAGCCTGGGCAACA | 6709 |
rs574639076 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583667 | CTTTCTCTTTGTGAC[A/C]TAAGTGAAGGAATAA | 6709 |
rs574661935 | snp | C/T | 5.20395e-05 | 0.00510069 | downstream-variant-500B, utr-variant-3-prime | SPTAN1, WDR34 | GRCh38.p7 | 9:128633728 | GCGAAGGCTTGCACC[C/T]GCCTCCCGGGACCCC | 6709 |
rs574696443 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590346 | TGCAGTAACTACTAG[A/C]TACGTGTGATAGTAA | 6709 |
rs574740801 | snp | A/G | 8.27041e-05 | 0.00643002 | missense | SPTAN1 | GRCh38.p7 | 9:128605470 | CAGCGCTTCCTTAGC[A/G]ATTTCCGGTACGGAG | 6709 |
rs574768274 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128556889 | ATCTGAGAATCAACT[A/G]GTATACAATTTTATG | 6709 |
rs574768316 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588457 | GCTGGGATTACAGGC[A/T]CGCACCACCACGCCT | 6709 |
rs574821774 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586644 | GTACATACCAGTGCG[C/G]ACATATACCCACATA | 6709 |
rs574867513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592788 | TGAAGGTGAACTAAC[C/T]CTCTAATTTTCCTGC | 6709 |
rs574872602 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599479 | AAAAGACAAAAAAAG[A/T]TGGTTTTTTTTTTTT | 6709 |
rs574880089 | snp | A/T | 0.000134046 | 0.00818566 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630201 | CCAGTTGCAGTTAGG[A/T]TTGGTTTCCTTAAAA | 6709 |
rs574894574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557782 | CATGCTGTATCTTTG[A/G]ATTAAATTAGAAATT | 6709 |
rs574954259 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574976 | GCTCTCTAGGTGTAT[A/G]TGCTATTCTGTAACT | 6709 |
rs574958192 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604608 | AGTTATTGGTGGTAG[C/T]CACAGACAAATATAC | 6709 |
rs574990297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609929 | ACAGTGTTTGATTTG[C/T]GGGGCAGTAATTGAC | 6709 |
rs574999355 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558255 | TGCTTTATCCCCCTG[A/T]GATTCGCATTACTTG | 6709 |
rs575068892 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572710 | AAGGTGGGTGGCATG[A/T]GAGGGCATGTCTGTG | 6709 |
rs575132798 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573411 | AGTTTTTTCTATCAG[G/T]GATCCTTTTTGATAG | 6709 |
rs575138747 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560067 | AGAAATGATTAATAC[A/G]TCCACATCCACCTCA | 6709 |
rs575218520 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128552308 | CTCACTGCACCATCA[C/T]CCCTCACCCCTTGCG | 6709 |
rs575246585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559368 | GGAACCTTTGCGATA[C/T]TATGATGGAGATTTT | 6709 |
rs575341120 | snp | A/G | 1.64974e-05 | 0.00287201 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611891 | AGGAAGATGACCACC[A/G]TCACTGTCAACCTGA | 6709 |
rs575368320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613945 | AGGAGGCGGAGGTTG[C/T]GGTAAGCCAAGATCG | 6709 |
rs575370160 | snp | C/T | 1.66109e-05 | 0.00288187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621143 | AATAGTGTGCCTTGG[C/T]TGCTTCTACTCCAGG | 6709 |
rs575384807 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565567 | CAATGAGAACTGCTT[C/G]AATCCCTACAGAGCT | 6709 |
rs575432805 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604902 | TGTGCATTGTGCTCC[A/T]GCCTGGGTGACAAGA | 6709 |
rs575440405 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564909 | AAGAATACTTCTATC[C/T]GCCACAAGGGTAGGG | 6709 |
rs575503127 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580105 | ATTGCTTGAGGCCAG[C/G]AATGGGAGACCATCC | 6709 |
rs575530162 | in-del | -/TT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613367 | CCTTTGCTTTTTGTG[-/TT]TTTTCATTGCCAGGT | 6709 |
rs575539535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594547 | GTGGTTCTCCTGCCT[C/T]AGCATCCTGAGTTGC | 6709 |
rs575579565 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624970 | GGCCTGCTAATGTGG[G/T]TTCTGAGGCTGTAGT | 6709 |
rs575582407 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604869 | CCGGTGGGGGCGGAG[G/T]TTGCAGTGAGCTGAG | 6709 |
rs575591355 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573954 | GAGATGGGGTTTCAC[C/T]ATGCTGGCCAGACTG | 6709 |
rs575642896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618730 | TCTCGTGATCTGCCC[A/G]CCTCGGCCTCCCAAA | 6709 |
rs575724057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568237 | ACTGCTTTAGGTACA[A/G]TCCCTGCCTGGCAGG | 6709 |
rs575760850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587949 | CTCCTGGGTTCAAGC[A/G]ATTTTCCTGACTCAG | 6709 |
rs575834494 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128552922 | AGGCTCGGCGCCGCC[C/G]CTGGAATGTCACTGA | 6709 |
rs575960602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583397 | GTGGATGACTTTGGC[A/G]TTAGGGATAATTTCC | 6709 |
rs576006336 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596757 | AGGGCAGTGGATGAT[A/C]ATAGCTCACTGTAAC | 6709 |
rs576010789 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621707 | CAGCCGCAGACTCCC[A/G]TTTAATAGGATCATA | 6709 |
rs576013207 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575970 | AAATTTTAAGTGTAT[A/T]AATCTGCTTATAGGC | 6709 |
rs576091601 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625206 | CCCCTTCACTGGTTG[A/T]AATGTATGCAGATAG | 6709 |
rs576096822 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128633048 | GTAACAGGCCCTGCG[C/G]TGGGTATTCTCCCCA | 6709 |
rs576102049 | snp | C/T | 0.00239473 | 0.03452 | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633620 | CACCCTCCCCCAAAT[C/T]TGTTTTCATGTAAAA | 6709 |
rs576106278 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563225 | GTTCGAGACTAGCCT[A/G]GGCAACATGGTGAAA | 6709 |
rs576117747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621971 | GAGGTTTTAACAGCT[A/G]TGGTTTCCTGTCACA | 6709 |
rs576118286 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561813 | CTAAATTACCTGTCT[C/G]CCAACTACTTAATTA | 6709 |
rs576136459 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601871 | CCTCATTAAGTAGAT[A/T]TCTAACTGGGCCAGG | 6709 |
rs576149656 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554155 | GCCTTTTTTAGTAAC[G/T]GGGCCAATAATTACT | 6709 |
rs576155124 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589962 | CACCCCACAGGCTTT[A/G]TCTTCTTTAGGCTAA | 6709 |
rs576183398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554946 | TCTACTTTGTGGCAA[C/T]TTCATGAAGTCATGC | 6709 |
rs576211164 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589604 | TTTTTGAGACAATGT[A/C]TTGCTCTGTCGTCCA | 6709 |
rs576224099 | in-del | -/T | 0.0174175 | 0.0916809 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602222 | TTTGGGTTTTTTTTG[-/T]TTTTTTTTTTTTGAG | 6709 |
rs576241909 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562619 | TTATAGTGATCCTTG[A/T]CAGGGTCCTCATCAG | 6709 |
rs576263230 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561391 | AAAAAAGGCCAGGCG[C/T]GGTGGCTCACGCCTG | 6709 |
rs576279414 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607444 | AAAAATAACAAGAAG[A/T]TTTTTAACACTTTGC | 6709 |
rs576282467 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595105 | GTAAGCCACCGTGCC[C/T]GGCCTCAGTTTTTTT | 6709 |
rs576419070 | snp | A/G | 3.29984e-05 | 0.00406179 | missense | SPTAN1 | GRCh38.p7 | 9:128608937 | GCCGGCCATTATGCC[A/G]AGGGAGACATTTCTA | 6709 |
rs576423643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597121 | GCCATGATCACGCCA[C/T]TGCACTCCAGTCTGG | 6709 |
rs576430741 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611083 | TACAAGCAGATTCAA[A/T]ACTGAAGTTGGCCAT | 6709 |
rs576442406 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602691 | CCCAGGCTGGAGTGC[A/T]GTGGCGCAATCTCAG | 6709 |
rs576482607 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603187 | TTTGTTAAATTTAGG[G/T]TTTTTTTTTTTCCGG | 6709 |
rs576499039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128556942 | GTTTGTTCTTAGGGA[A/G]GCCCTTCCACATCCA | 6709 |
rs576516530 | snp | A/C | | | missense | SPTAN1 | GRCh38.p7 | 9:128583194 | AAGCTGATTGATGTC[A/C]ACCACTATGCCAAGG | 6709 |
rs576561502 | in-del | -/GAATCACACAT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618347 | TTCTGTATGAGTCCA[-/GAATCACACAT]GAATCACACATGAAT | 6709 |
rs576572420 | in-del | -/CTA | 0.00517822 | 0.0506191 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572260 | TGCTTGCTTATGTCC[-/CTA]CTGAGAAATCCACCT | 6709 |
rs576636314 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624675 | CCAGAACTGCCACCC[A/G]GAACTGGGCTGGCAC | 6709 |
rs576636320 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587473 | GATATTAGCACTGTA[A/C]GAAGGGCAGGAGGTG | 6709 |
rs576694834 | snp | C/G | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554204 | GTGTTAACTGTTATC[C/G]AGGGACCTTGATGGA | 6709 |
rs576697679 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589736 | GCCTGCCACCACGCC[C/T]GGCTAATTTTTTGTA | 6709 |
rs576723855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571731 | ATTATTTCCCTATTA[C/T]GTGAGAGTAGAAACT | 6709 |
rs576843851 | snp | A/C | 8.57479e-05 | 0.00654726 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624508 | CACTGTCAGCAAGGC[A/C]CGGAAGAGCCTTCCC | 6709 |
rs576858834 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564195 | GGAGGCCAAGGCGGG[G/T]GGATCACGAGGTCAG | 6709 |
rs576864516 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579008 | GTCTAACAAAAGAGT[A/G]TAAGACACTTCTGGA | 6709 |
rs576905399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630833 | CCTCAACCTCCCAAG[C/T]AGCTGGGATTACAGG | 6709 |
rs576930189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585404 | GGGGAGTAAGTGAAA[C/T]CAAGTAGGAAAAGAG | 6709 |
rs576966005 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631446 | CCTGGGTGACAAGAG[C/G]AAAACTCCCTCTGAA | 6709 |
rs576995498 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578450 | GTTCAGTGTCAAGAG[A/G]TTCACTGTGGTCCAT | 6709 |
rs577001164 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571162 | GGGCGTGGTGGTGCA[C/T]ACCTGTAGCCCCAGC | 6709 |
rs577072603 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587157 | GTGATGCAATCACGA[C/T]TCCCTACAGCTTTGA | 6709 |
rs577128759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580209 | GTCCGAGCTACTTGA[A/G]TTCAAGGTTATAATG | 6709 |
rs577176123 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575128 | CCCTAATGTGTCTGT[C/T]TGATGTTTCTGGAAG | 6709 |
rs577258071 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588038 | TTTTTTTGAGATGGA[A/G]TCTTGCTAGAGTGCA | 6709 |
rs577295584 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560842 | GCCAATATGGTGAAA[C/T]CCAATCTCTACAAAA | 6709 |
rs577306590 | snp | C/T | 1.6679e-05 | 0.00288777 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625197 | CTGCCCTGGCCCCTT[C/T]ACTGGTTGAAATGTA | 6709 |
rs577370564 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128551131 | CCAGATTCTGGTGCA[C/G]TGTCCAATGACTTTA | 6709 |
rs577372283 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566310 | AGTCTGCCACTTTGG[A/C]CTCCCAAAGTGTTGG | 6709 |
rs577417059 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586755 | TTCATAAAGGTCTAG[G/T]TATAGTTCCTGTACC | 6709 |
rs577428232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604819 | GCCTGTAATCCTAGC[C/T]ACTTGGGAGGTTGAG | 6709 |
rs577481625 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598052 | CTACCGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 6709 |
rs577494787 | in-del | -/A | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128556220 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAATTAA | 6709 |
rs577541510 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594580 | GGATTACAGATGTGC[A/G]TCACCACGCCCTGCT | 6709 |
rs577553241 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592887 | TCCCAACATTAAGCA[G/T]CCACCATCATGGCAC | 6709 |
rs577603661 | snp | A/G | 0.000399281 | 0.0141238 | missense | SPTAN1 | GRCh38.p7 | 9:128607611 | GTTTCCAGGGACCTC[A/G]TGTCTTGGATCAATG | 6709 |
rs577644334 | snp | A/C | 0.0126979 | 0.078662 | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128552373 | CCTCGCTCACCTCTT[A/C]CCCCGCATTGTCGCT | 6709 |
rs577681658 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614602 | CTCAAAAAAAAAACA[A/C]AAAAAAAACACAAAA | 6709 |
rs577707381 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596056 | GCCATGTTGCCCAGT[C/G]TGGTCTCAAACTCCT | 6709 |
rs577730526 | snp | A/G | 5.02871e-05 | 0.00501408 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632228 | GGACAACAAGTACAC[A/G]GAGCACAGCACCGTG | 6709 |
rs577739348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615182 | TATTCTGGACCGAGT[A/G]TCTGTGAGATACCAA | 6709 |
rs577861477 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573550 | CAACCTCCACCTCCC[A/T]GGTTCAAGCAATTCT | 6709 |
rs577894230 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568099 | AAAGCCTTTCTTCTC[A/G]CTTATTTCAGTGAAA | 6709 |
rs577900415 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605975 | CCAGCCCGGGCAACA[A/G]GAGTGAAACTCCATC | 6709 |
rs577910841 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613708 | ACCATTATTAAAAAT[G/T]ACATAAATTTTAAGG | 6709 |
rs577918700 | snp | C/T | 6.63372e-05 | 0.00575884 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588770 | ATGACTCAGCGCGGA[C/T]GTGTTTTTACCATGT | 6709 |
rs577918713 | snp | A/G | 4.99654e-05 | 0.00499802 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581933 | TCAAATGACCCTTAT[A/G]GTAAGCCAGAGTCTT | 6709 |
rs578008227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621899 | AGTGTGTCCGTGGGT[C/T]GGGAATTCACCAGCA | 6709 |
rs578034901 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627293 | GGGAGGTTCCTTGTG[A/G]GGAGGCCACCACCAC | 6709 |
rs578124150 | snp | A/G | 0.00025365 | 0.0112588 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128621241 | CTGCACCAATGGACA[A/G]GACCTCATTAAGAAG | 6709 |
rs578145741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574982 | TAGGTGTATGTGCTA[C/T]TCTGTAACTCTGAAG | 6709 |
rs578253313 | snp | A/G | 0.00164622 | 0.0286427 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609092 | CGGTAAGATATGCTC[A/G]TGTTGGATCTCATGG | 6709 |
rs587784431 | snp | C/T | 1.64868e-05 | 0.00287109 | SPTAN1 | 9 | allele_origin=T(germline)/C(germline) | 9:128580987 | GCGCAGGCAGCAGTA[C/T]GAGCAGTGCATGGAC | 6709 |
rs587784432 | snp | C/G/T | 1.64743e-05 | 0.00287 | SPTAN1 | 9 | allele_origin=G(germline)/C(germline) | 9:128582720 | CCGCAATGCCCTTCA[C/G/T]GAGAGAGCCATGCGT | 6709 |
rs587784433 | snp | A/G | | | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128583840 | TAATCGCAATGTTGA[A/G]GATATTGAATTGTGG | 6709 |
rs587784434 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584708 | ATAACTGGGGACTGG[G/T]GTCTGCTTTCAGGTA | 6709 |
rs587784435 | snp | G/T | | | missense | SPTAN1 | GRCh38.p7 | 9:128585861 | GAGGACTCTCTGCAG[G/T]CCCAGCAGTACTTTG | 6709 |
rs587784436 | snp | C/T | | | missense, intron-variant | SPTAN1 | GRCh38.p7 | 9:128593020 | GGCAGTGTATCTCTG[C/T]GTATGAAGCAGGTGG | 6709 |
rs587784437 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615622 | GACCCTCTTATGTCC[C/T]CTGCCCCAGGATCGC | 6709 |
rs587784438 | in-del | -/GAG | | | cds-indel | SPTAN1 | GRCh38.p7 | 9:128627428 | CAGCGGCGGCAGGAG[-/GAG]AACGACAAGCTGCGC | 6709 |
rs587784439 | snp | C/T | 1.90015e-05 | 0.00308227 | SPTAN1 | 9 | allele_origin=T(germline)/C(germline) | 9:128632120 | TCTGTGCTCCCCACC[C/T]CTGCAGCGCAAGCAC | 6709 |
rs587784440 | in-del | -/GGACCAGCT | | | cds-indel | SPTAN1 | GRCh38.p7 | 9:128632278 | CAGTGGGACCAGCTG[-/GGACCAGCT]TGGGCATGCGCATGC | 6709 |
rs587784441 | in-del | -/ACCAGCTGG | | | cds-indel | SPTAN1 | GRCh38.p7 | 9:128632280 | AGCTGGACCAGCTGG[-/ACCAGCTGG]GCATGCGCATGCAGC | 6709 |
rs587784442 | snp | C/T | 0.000329663 | 0.0128344 | SPTAN1 | 9 | allele_origin=T(germline)/C(germline) | 9:128577400 | CAACAGTCCCACCCT[C/T]TGAGTGCAACACAGA | 6709 |
rs745319868 | snp | A/C | 1.64895e-05 | 0.00287132 | missense | SPTAN1 | GRCh38.p7 | 9:128609265 | GTGATGAGTCGTACA[A/C]GGATCCCACCAACAT | 6709 |
rs745379624 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626730 | GCTCGGCCTCCCAGA[A/G]CCCTCTCTGGGCCCT | 6709 |
rs745384778 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632090 | GTGACTGAGCTGAGG[A/G]CCCCCGTCTGAGCAT | 6709 |
rs745394212 | snp | A/G | 1.64746e-05 | 0.00287002 | missense | SPTAN1 | GRCh38.p7 | 9:128609130 | CTTTCAGGTGGCGAC[A/G]TCTGAAAGCCCAGAT | 6709 |
rs745402857 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613819 | GACCACTCCGGCCAA[C/T]GTGGTGAGACCTCCG | 6709 |
rs745430813 | snp | C/G/T | 4.94184e-05 | 0.00497063 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591455 | AGGAATTTACTTTCA[C/G/T]TTCTCCCTCTTTTTT | 6709 |
rs745436802 | snp | C/T | 3.30622e-05 | 0.00406571 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128584374 | GAAACAGGAAGCCCT[C/T]GTGGCTCGCTATGAG | 6709 |
rs745454196 | snp | A/G | 1.6476e-05 | 0.00287014 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582565 | AGATGCTGTAAGTTT[A/G]TAGGTTCTTCATGCT | 6709 |
rs745456138 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628790 | AGAGCAGCTGGGGAC[A/G]TAGGGATCGCAGTTT | 6709 |
rs745471364 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599273 | CTGAGTAGCTGGAAT[G/T]CCACGCATGTGGCAC | 6709 |
rs745477060 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592597 | ATTCTTACCAGTAGT[A/C]TGGGTCATAAATATA | 6709 |
rs745483287 | snp | C/T | 1.73966e-05 | 0.00294924 | downstream-variant-500B, intron-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128634034 | TCTAGAGACCAACCA[C/T]ATGGCAGGAGGAGGC | 6709 |
rs745494941 | snp | C/T | 0.000125329 | 0.0079151 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626703 | GTACACCTCCCGCTG[C/T]CCTCAGGAGCTGCTC | 6709 |
rs745514857 | snp | A/G | 1.64882e-05 | 0.00287121 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128619003 | TCTTGCCGCCATCCA[A/G]GTGAGACAGAAACCA | 6709 |
rs745529207 | snp | C/T | 3.30136e-05 | 0.00406273 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128605448 | GTTGGGTGACTCCCA[C/T]GACCTGCAGCGCTTC | 6709 |
rs745538318 | snp | C/G | 1.6646e-05 | 0.00288491 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582430 | TCTCCAGAGGCCAAG[C/G]TTGGGACTAGTGTGC | 6709 |
rs745542418 | in-del | -/T | 5.1989e-05 | 0.00509822 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576786 | TGGAGGAGCCAGAAG[-/T]TGTGTACAAATCCAG | 6709 |
rs745544548 | snp | C/G | 3.30415e-05 | 0.00406444 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584560 | GTAGGAATCAACTTG[C/G]GAAAGGCTGTGCTAT | 6709 |
rs745580923 | snp | C/G | 1.67587e-05 | 0.00289466 | missense | SPTAN1 | GRCh38.p7 | 9:128632219 | CCTCATCCTGGACAA[C/G]AAGTACACGGAGCAC | 6709 |
rs745582924 | snp | A/G | 1.68224e-05 | 0.00290016 | missense | SPTAN1 | GRCh38.p7 | 9:128626590 | TGGCCGAGCTGGACC[A/G]CCAGATCAAGAGCTT | 6709 |
rs745625336 | snp | G/T | 1.64764e-05 | 0.00287018 | splice-donor-variant | SPTAN1 | GRCh38.p7 | 9:128600117 | CCTCCCCGTGGAAGG[G/T]AAGAACTCCTTTGCA | 6709 |
rs745633888 | snp | A/C | 1.64743e-05 | 0.00287 | missense | SPTAN1 | GRCh38.p7 | 9:128578134 | CTTCCTTGCTGACTT[A/C]CGTGACCTCACCAGC | 6709 |
rs745668882 | snp | C/G/T | 3.32515e-05 | 0.00407736 | missense, synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128624424 | CAGAGAAAGGCGAAG[C/G/T]TGGATGAGAACTCGG | 6709 |
rs745670418 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605774 | AGGCGGGCAGATCAC[C/T]TGAGGTCAAGAGTTC | 6709 |
rs745673891 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587782 | TTCCTATCATAGGCC[C/T]CATTTGACTCTGCTA | 6709 |
rs745682285 | snp | C/G | 1.64738e-05 | 0.00286995 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627981 | CTGGGCTTGTCATGT[C/G]GGGGTCTCGTGCGCT | 6709 |
rs745697305 | snp | C/G | 1.64765e-05 | 0.00287019 | missense | SPTAN1 | GRCh38.p7 | 9:128607948 | CACTATGCCAGCCCT[C/G]AGATCAAGCAGAAAC | 6709 |
rs745720603 | snp | A/C | 1.65405e-05 | 0.00287576 | missense | SPTAN1 | GRCh38.p7 | 9:128582842 | CTGCCACAGATGAAG[A/C]TTATAAAGTAATGTA | 6709 |
rs745729487 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562248 | GCTGGGGCTACAGGC[C/G]CGTGCCACCACACCC | 6709 |
rs745746027 | snp | C/G | 1.64798e-05 | 0.00287047 | missense | SPTAN1 | GRCh38.p7 | 9:128585883 | AGTACTTTGCTGATG[C/G]TAACGAGGCTGAATC | 6709 |
rs745750589 | snp | A/G | 0.000164728 | 0.00907398 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128630339 | CTGTATGGTGGAAGA[A/G]TCGGGGACCCTCGAA | 6709 |
rs745751324 | snp | C/T | 1.65255e-05 | 0.00287445 | missense, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633281 | GGCAAGGGCCGCGAG[C/T]TCCCCACCGCGTTCG | 6709 |
rs745772162 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600330 | CAGTACAGTTAGGTT[A/G]CATTGATTACCCATG | 6709 |
rs745775253 | snp | C/G | 1.66866e-05 | 0.00288842 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615852 | TCAAGTATGTCTTCT[C/G]AGCCCTCTAGAAGGC | 6709 |
rs745793103 | snp | A/C | | | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128550586 | GTCTCCATTTTGCAT[A/C]CAGCAAAAGCAGCAG | 6709 |
rs745798632 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | SPTAN1 | GRCh38.p7 | 9:128603562 | CTCGTCTGATGGTTC[A/G]CACCGTGGCCACCTT | 6709 |
rs745798837 | in-del | -/CTCT | 8.25191e-05 | 0.00642283 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630241 | GGTTGCCAGGCATTG[-/CTCT]CTCTGAGAGAAGGTT | 6709 |
rs745819476 | snp | C/T | 1.67449e-05 | 0.00289347 | splice-donor-variant | SPTAN1 | GRCh38.p7 | 9:128588945 | ACAGCACCAACAAGG[C/T]AAGGCACAGAGAGTG | 6709 |
rs745828218 | snp | A/G | 3.3173e-05 | 0.00407252 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578297 | TTTAGCTTATAATGC[A/G]CCAGTTTATCAGTGT | 6709 |
rs745841634 | snp | C/T | 4.94189e-05 | 0.00497062 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630287 | TCGGCCAGCTGGGAG[C/T]AGGCCCCTTTCCTCA | 6709 |
rs745887395 | snp | A/G | 4.95086e-05 | 0.00497512 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128611749 | GGCTTTTGAAGCAGA[A/G]CTGCATGCCAACGCT | 6709 |
rs745910160 | snp | C/T | 3.04298e-05 | 0.00390051 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592973 | CTTTTGCTGTGCCCC[C/T]TCTGTGCAGGACACG | 6709 |
rs745921302 | snp | A/C | 1.6473e-05 | 0.00286988 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612250 | TGGCTGTCTGAGGTA[A/C]CACTGAGTGGTTCCT | 6709 |
rs745928422 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581766 | TTATTCTGAACACTT[C/T]GTTTCCTTTGGCAAG | 6709 |
rs745946054 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597959 | CGGCCTGTTTTGTTT[C/T]GTTTTTGAGATGGAG | 6709 |
rs745968866 | snp | C/T | 4.97418e-05 | 0.00498682 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626358 | CACGTCCAGCCCTGG[C/T]GACTCCGCCAACTCA | 6709 |
rs745995736 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567823 | TGGAGTGCAATGGTG[C/T]AATCTCAGCTCACTG | 6709 |
rs745997127 | snp | A/G | 6.59196e-05 | 0.00574068 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128605130 | TGTCCAGGCCCTGCA[A/G]CGCAAGCATGAGGGC | 6709 |
rs745999155 | snp | A/G | 4.97929e-05 | 0.00498939 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591665 | AGGGCTAGGCGTCCC[A/G]TAGGCATACTCTGTT | 6709 |
rs746027373 | in-del | -/AG | 1.73111e-05 | 0.00294198 | downstream-variant-500B, intron-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128634019 | GGAGTAAGAGAAACT[-/AG]CTAGAGACCAACCAC | 6709 |
rs746030790 | snp | C/T | 3.29451e-05 | 0.00405851 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627880 | ATTGCTGCTGTTGTC[C/T]GGACACCACCTTGTC | 6709 |
rs746049622 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579528 | TTCATTTTGTTTCTC[A/G]TTTTAGATGTCATAG | 6709 |
rs746051866 | snp | A/C | 1.64961e-05 | 0.00287189 | missense | SPTAN1 | GRCh38.p7 | 9:128632604 | AGTCTGGCAGGCTGA[A/C]CCATCAGGAGTTCAA | 6709 |
rs746073412 | snp | C/G | 1.64849e-05 | 0.00287092 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607841 | CCTAATCCCTTCCCT[C/G]CTTTTGGCAGGAACA | 6709 |
rs746096234 | snp | C/T | 1.65548e-05 | 0.002877 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128585758 | TCCAGGCCATTTTGC[C/T]GCAGAGGATGTGAAG | 6709 |
rs746115051 | snp | C/T | 1.65119e-05 | 0.00287327 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128576897 | GCAGCGGCTGAAGGG[C/T]CTGGCTCTGCAGAGG | 6709 |
rs746115201 | snp | A/C/G | 4.9504e-05 | 0.00497493 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632535 | GGTGTTCGGCAGCAG[A/C/G]GCTGCCTGCTGAGCC | 6709 |
rs746125020 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625254 | GTGGCGTCTTTCACT[A/G]AGGCATTTATCTTCT | 6709 |
rs746126982 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566637 | ATTCATTTGTCTCCT[A/G]GGTTTATCTGATAAT | 6709 |
rs746152161 | snp | C/T | 1.65162e-05 | 0.00287365 | missense | SPTAN1 | GRCh38.p7 | 9:128608914 | CCTTTGCCGACCAGC[C/T]CATCGCTGCCGGCCA | 6709 |
rs746165535 | in-del | -/G | 1.66432e-05 | 0.00288467 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583050 | CTCAGGTTCAAGATA[-/G]AAAGAACCCCCTTCT | 6709 |
rs746188119 | snp | A/T | 1.65847e-05 | 0.0028796 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588769 | GATGACTCAGCGCGG[A/T]CGTGTTTTTACCATG | 6709 |
rs746207210 | snp | A/G | 1.64849e-05 | 0.00287092 | missense | SPTAN1 | GRCh38.p7 | 9:128583833 | AGCAATTTAATCGCA[A/G]TGTTGAGGATATTGA | 6709 |
rs746212419 | in-del | -/ATAT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606473 | TATTTTTCCCTAGAC[-/ATAT]ATATATATATATTTT | 6709 |
rs746219199 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606629 | GCTGGGATCACAGGC[A/G]TGCACCACCAAGCCC | 6709 |
rs746222854 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560885 | GTCGCGTGTGGTGGC[A/G]GGTGCCTGTAATCCC | 6709 |
rs746224717 | snp | A/G | 3.34594e-05 | 0.00409006 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566987 | TTGCAGGTACGTCTG[A/G]TCTCCTGGGATTCCT | 6709 |
rs746241176 | snp | A/G | 1.68957e-05 | 0.00290647 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632974 | TGGGCCTCAGGAGGT[A/G]GGTGAAGAGGTGTCC | 6709 |
rs746241694 | snp | C/T | 3.36905e-05 | 0.00410416 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613516 | CGGGCCAGGCCCGAG[C/T]GCCTGGGACACAGCT | 6709 |
rs746247011 | snp | A/G | 7.06739e-05 | 0.00594407 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628176 | CGTCCTTGCCTCACT[A/G]GGCGATTCCAAGGGC | 6709 |
rs746280203 | snp | C/T | 8.23649e-05 | 0.00641683 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598995 | GCCCAGGGTAAGTTT[C/T]GGGTGCTGTGTGTGG | 6709 |
rs746285126 | snp | C/G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623982 | CAGCTACTCGGGAGG[C/G/T]TGAGGCAGGAGAATC | 6709 |
rs746307611 | snp | C/G | 1.65239e-05 | 0.00287431 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581097 | CCAGTGGTGGGAGAA[C/G]AAGGGCCTGTGTTTT | 6709 |
rs746309277 | snp | C/G/T | 8.59197e-05 | 0.00655391 | downstream-variant-500B, utr-variant-3-prime | SPTAN1, WDR34 | GRCh38.p7 | 9:128633735 | CTTGCACCCGCCTCC[C/G/T]GGGACCCCTCAGGCC | 6709 |
rs746311922 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591085 | TTTTTTTTATGAGAC[A/G]GAGTCTCGCTCTGAC | 6709 |
rs746335136 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603081 | CCTTCAACGGGGATA[C/T]GGTTAAAAAGAACAG | 6709 |
rs746345701 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585506 | TACTATCACTAATGC[C/T]AACTTGCGATATCTG | 6709 |
rs746364511 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612487 | TCCATAGGGAAGGCA[A/T]ATAGGAAGAGATTAT | 6709 |
rs746367287 | snp | G/T | 1.65239e-05 | 0.00287431 | missense | SPTAN1 | GRCh38.p7 | 9:128625945 | AGCCGCCCGCAAGAA[G/T]AAGCTTCTGGAGGCT | 6709 |
rs746369946 | snp | C/T | 1.65042e-05 | 0.0028726 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605020 | TTCTTAACCTGAATG[C/T]GTCTCGCCTTTAGAG | 6709 |
rs746373075 | snp | A/G | 3.29881e-05 | 0.00406115 | missense | SPTAN1 | GRCh38.p7 | 9:128608956 | GAGACATTTCTAGCC[A/G]GCGCAATGAGGTCTT | 6709 |
rs746376242 | in-del | -/CTG | 1.68927e-05 | 0.00290622 | downstream-variant-500B, cds-indel | SPTAN1, WDR34 | GRCh38.p7 | 9:128633758 | CTCAGGCCGCCACCT[-/CTG]CTGCCAGGCAGTCCA | 6709 |
rs746382393 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559538 | CTCGTGTGCAGTGTC[A/G]TTATTGTTCCATGTG | 6709 |
rs746443349 | snp | A/C | 3.52355e-05 | 0.0041972 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630141 | AAAACGGGAGAAATG[A/C]TCCCTGCCATCCCTC | 6709 |
rs746448578 | snp | C/T | 1.64863e-05 | 0.00287104 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608996 | GGTGTCCTGTGGCAC[C/T]GACATAGTCACCAGC | 6709 |
rs746490684 | snp | A/G/T | 3.29561e-05 | 0.00405921 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128568873 | GATGATCTCAGAAGG[A/G/T]CATTTTGCATCTGAA | 6709 |
rs746501410 | snp | A/G | 1.65416e-05 | 0.00287586 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578276 | GAATCTTCCAGAAGT[A/G]AAGATTTTAGCTTAT | 6709 |
rs746521266 | snp | A/C/T | 4.9433e-05 | 0.00497137 | missense | SPTAN1 | GRCh38.p7 | 9:128615731 | GACACCATCAACGGG[A/C/T]GCTTCCAGAAGATCA | 6709 |
rs746532292 | snp | A/C/T | 8.29874e-05 | 0.00644109 | missense, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633216 | CCCCACAGAACCTGA[A/C/T]CCGGGAACAAGCCGA | 6709 |
rs746536511 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626086 | GAAGCTGTGAGCTCA[A/G]TGCAGAGCTTTCAAA | 6709 |
rs746548283 | snp | A/C | 3.29495e-05 | 0.00405877 | missense | SPTAN1 | GRCh38.p7 | 9:128600084 | TCTTTGAATAGGATG[A/C]AACTGATTCCAAGAC | 6709 |
rs746555665 | snp | A/C | 0.000121647 | 0.007798 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624522 | CCCGGAAGAGCCTTC[A/C]CAGAGCTGCTCTTTG | 6709 |
rs746570112 | snp | A/C | 1.65501e-05 | 0.00287659 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588801 | TTGCCCTTCCTTTGG[A/C]TTTTTAGCAACAAGT | 6709 |
rs746575696 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625551 | CCTGGGGCGGGAGAG[C/T]GGAAGGCTGGGGTCA | 6709 |
rs746651127 | snp | A/T | 0.000346892 | 0.0131653 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626386 | TCAGTCTCTTCTGCT[A/T]CCAGGTGGAGGACCT | 6709 |
rs746658912 | snp | C/G | 3.295e-05 | 0.00405881 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609115 | TCTCATGGTTTCACT[C/G]TTTCAGGTGGCGACG | 6709 |
rs746674327 | snp | A/G | 9.91441e-05 | 0.00704004 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128584365 | CATCAAGAAGAAACA[A/G]GAAGCCCTCGTGGCT | 6709 |
rs746712451 | snp | A/T | 1.65064e-05 | 0.00287279 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574649 | CCAGTTGTGATCTGA[A/T]TAAAACTCTGATTTG | 6709 |
rs746716379 | in-del | -/C | | | downstream-variant-500B, utr-variant-3-prime | SPTAN1, WDR34 | GRCh38.p7 | 9:128633676 | AGCTTTGCTTTTCTT[-/C]CATTTGGCTTGCGTC | 6709 |
rs746720655 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585104 | AGTGGAACCTCTGCT[C/T]CCCTAGTTCAAGCAG | 6709 |
rs746757640 | snp | C/T | 1.64879e-05 | 0.00287118 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607827 | TCTGCTGCCAGTTAC[C/T]TAATCCCTTCCCTCC | 6709 |
rs746784415 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598814 | AAGTTTATATATAAA[A/T]ACTTGAAGCTCTGCT | 6709 |
rs746824729 | snp | A/G | 0.000115905 | 0.00761176 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128611725 | TTAGAGCAAGCACCA[A/G]AAGCACCAGGCTTTT | 6709 |
rs746833835 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613311 | GAATAGCCACTGGGC[A/G]ACCTGAATTTTCCAG | 6709 |
rs746834111 | snp | A/G | 6.59076e-05 | 0.00574016 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584846 | ATGGTGGAGGAAGGT[A/G]AGTGATTGGTATCAG | 6709 |
rs746886442 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572797 | GCGCCCCATAGTCAC[C/G]GCCACCCACATCGGG | 6709 |
rs746905318 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597802 | ATTACAGGCGCCTGC[C/T]ACCGCGCCTAGCTAA | 6709 |
rs746913959 | snp | A/G | 1.64776e-05 | 0.00287028 | missense | SPTAN1 | GRCh38.p7 | 9:128607930 | CAGCTGTTGGCTCAC[A/G]GACACTATGCCAGCC | 6709 |
rs746914596 | in-del | -/A | 1.64904e-05 | 0.00287139 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607802 | TCGGTGGTTGACGTC[-/A]GAGTGGGCATCTGCT | 6709 |
rs746956582 | snp | A/G | 4.94271e-05 | 0.00497102 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599020 | GTGTGGATCTTGAAC[A/G]TGAGAAGGACTTAAA | 6709 |
rs746961427 | snp | C/G | 3.29881e-05 | 0.00406115 | missense | SPTAN1 | GRCh38.p7 | 9:128582808 | GAGCTCAAGAGTTGG[C/G]TCAATGAGAAGATGA | 6709 |
rs746969548 | in-del | -/T | 1.64734e-05 | 0.00286992 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618851 | TTATGGCTGATTTTC[-/T]TCCTGTCTCCTGTAA | 6709 |
rs746979666 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598928 | AGATGTGTATTTCTT[C/T]TAATAATAAAACTGG | 6709 |
rs746993013 | snp | A/G | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554191 | GGACCCTCAAAGTGT[A/G]TTAACTGTTATCCAG | 6709 |
rs747006735 | snp | C/T | 9.34973e-05 | 0.00683666 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627642 | CTGGCAACGCCTGGT[C/T]GGGCTCTGGAGCCGG | 6709 |
rs747039864 | snp | C/T | 1.65209e-05 | 0.00287405 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605006 | GTTGTACTTGGCATT[C/T]CTTAACCTGAATGTG | 6709 |
rs747085191 | snp | A/G | 1.64874e-05 | 0.00287113 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128580978 | GTGGGAGCTGCGCAG[A/G]CAGCAGTACGAGCAG | 6709 |
rs747129367 | snp | C/G | 1.76993e-05 | 0.00297478 | missense | SPTAN1 | GRCh38.p7 | 9:128604367 | ACAGCAGCTGGCCGA[C/G]GAACGGAGCCAGCTC | 6709 |
rs747147414 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565842 | TCTGCTTCCTTAGTG[A/C]ACTCAAAAACCTCTC | 6709 |
rs747171460 | snp | G/T | 0.000277098 | 0.0117674 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609643 | GTTCTTTTAATCTGT[G/T]TTTGTAGCTTTCCAA | 6709 |
rs747172506 | snp | C/T | 1.66418e-05 | 0.00288455 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575378 | GTATGCTTCTCACAA[C/T]ATTATTATGTTAACT | 6709 |
rs747183463 | snp | C/G | 1.64879e-05 | 0.00287118 | missense | SPTAN1 | GRCh38.p7 | 9:128583817 | GAAGCCAACCAGCAA[C/G]AGCAATTTAATCGCA | 6709 |
rs747186260 | snp | A/G | 1.65015e-05 | 0.00287237 | missense | SPTAN1 | GRCh38.p7 | 9:128632463 | CTGAGGAGGCCCTCA[A/G]AGAATTCAGCATGAT | 6709 |
rs747206756 | snp | A/G/T | 3.29779e-05 | 0.00406055 | missense | SPTAN1 | GRCh38.p7 | 9:128618017 | GGCAAGAAGCTGTCC[A/G/T]ATGACAACACCATCG | 6709 |
rs747220460 | in-del | -/AG | 1.72414e-05 | 0.00293605 | downstream-variant-500B, intron-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128633997 | CCTGCAAAGAGAGAC[-/AG]ATACGTGGAGTAAGA | 6709 |
rs747221955 | in-del | -/T | 1.69934e-05 | 0.00291486 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632999 | TGTCCTTTGGAAAAC[-/T]TAAAGCCAAATTTGT | 6709 |
rs747239106 | in-del | -/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564532 | GGTTGCAGTGAGCCG[-/T]TGACTGCACTCCAGC | 6709 |
rs747276507 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589489 | GAGATGGGGTTTCAC[C/T]GTGGTCTCTATCTCC | 6709 |
rs747281260 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622198 | GCTCCTGCACACTTA[A/G]CCCCCTGACACACAC | 6709 |
rs747282086 | snp | C/G | 1.66161e-05 | 0.00288232 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613365 | TAGCCTTTGCTTTTT[C/G]TGTTTTCATTGCCAG | 6709 |
rs747335429 | snp | C/T | 1.66308e-05 | 0.00288359 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587572 | GGGAGGCTTCAGCCC[C/T]TGCACAGTGCTCCAT | 6709 |
rs747335659 | snp | C/G | 1.91867e-05 | 0.00309725 | missense | SPTAN1 | GRCh38.p7 | 9:128598403 | TTTGCTTTAAAGGAC[C/G]TGAAGGCCAATGAGT | 6709 |
rs747409698 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581451 | GCACTCTAGCCTGTG[C/T]AACAGACCGAGATCC | 6709 |
rs747412785 | in-del | -/TG | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607586 | TAATAGCTATTTTTC[-/TG]GGGTGCTGGTTTCCA | 6709 |
rs747419719 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558686 | GGAACAGCCTGGAAC[A/G]TTCTCTGTGAAGTCG | 6709 |
rs747442396 | in-del | -/TAAAT | | | splice-donor-variant | SPTAN1 | GRCh38.p7 | 9:128632719 | GTGGATCCGAACAGG[-/TAAAT]TAAATTAATTAAGGC | 6709 |
rs747453186 | in-del | -/A | 1.64757e-05 | 0.00287012 | frameshift-variant | SPTAN1 | GRCh38.p7 | 9:128574775 | GTTGGTGCAGTACTT[-/A]ACGAGAATGTGAGGA | 6709 |
rs747480352 | snp | A/G | 1.71764e-05 | 0.00293051 | missense | SPTAN1 | GRCh38.p7 | 9:128583281 | GCCACTGAACTGAAA[A/G]GTAAGAGATGTTCCA | 6709 |
rs747501430 | snp | A/G | 1.67061e-05 | 0.00289011 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566982 | CCAACTTGCAGGTAC[A/G]TCTGATCTCCTGGGA | 6709 |
rs747510615 | snp | A/G | 1.65056e-05 | 0.00287272 | missense | SPTAN1 | GRCh38.p7 | 9:128566823 | TAGACCGATACCACC[A/G]CTTCAAGGAACTCTC | 6709 |
rs747529580 | snp | C/G | 1.64895e-05 | 0.00287132 | missense | SPTAN1 | GRCh38.p7 | 9:128587661 | GTGCCTACGGCAGCA[C/G]CATCCAGGCTTTGCG | 6709 |
rs747533383 | snp | A/C | | | downstream-variant-500B, intron-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128633999 | TGCAAAGAGAGACAG[A/C]TACGTGGAGTAAGAG | 6709 |
rs747546777 | snp | C/G/T | 6.73316e-05 | 0.0058019 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613512 | GAGGCGGGCCAGGCC[C/G/T]GAGTGCCTGGGACAC | 6709 |
rs747552940 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615115 | AAAAGTTTGAATTTT[A/G]TCATTAGTAACAAAC | 6709 |
rs747582018 | snp | C/T | 1.65575e-05 | 0.00287724 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632868 | CCGCGAAACTGAGAA[C/T]GTCAAGTCCAGCGAG | 6709 |
rs747590672 | snp | A/G | 1.69223e-05 | 0.00290876 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577524 | GCAAATAATGCTCCA[A/G]GTCTTAACCAGTATC | 6709 |
rs747612780 | in-del | -/ATAAAA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599855 | CATTTCTTCTACTGG[-/ATAAAA]AAATTGGAATTTTTC | 6709 |
rs747620583 | snp | C/T | 1.64741e-05 | 0.00286998 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599002 | GTAAGTTTCGGGTGC[C/T]GTGTGTGGATCTTGA | 6709 |
rs747645046 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603136 | TGAAAGTGATTATTA[A/G]AGCTCCTGGCTGTTA | 6709 |
rs747701235 | snp | C/T | | | missense | SPTAN1 | GRCh38.p7 | 9:128604393 | AGCTCTTGGGCAGCG[C/T]CCATGAAGTACAGAG | 6709 |
rs747710094 | snp | C/T | 1.64901e-05 | 0.00287137 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607814 | GTCAGAGTGGGCATC[C/T]GCTGCCAGTTACCTA | 6709 |
rs747717370 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573671 | ATGTTGGCCAGGCTG[C/G]TCTCGAACTCCCGAC | 6709 |
rs747719265 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559678 | GAACAAAGGAAATAT[A/G]TAAATAAATAAGTCT | 6709 |
rs747723552 | in-del | -/AT | 1.6477e-05 | 0.00287024 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607573 | TTACCAGGTAATATA[-/AT]AGCTATTTTTCTGGG | 6709 |
rs747787899 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581218 | TCTCAGCTCTGCCAG[C/T]ATCTCTCCCTGCTGA | 6709 |
rs747791505 | snp | C/T | 3.48141e-05 | 0.00417203 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630156 | CTCCCTGCCATCCCT[C/T]GATCCCTGGGGCCCA | 6709 |
rs747794736 | snp | C/T | 3.29554e-05 | 0.00405914 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128615727 | GAGGGACACCATCAA[C/T]GGGCGCTTCCAGAAG | 6709 |
rs747796809 | snp | A/G | 4.95381e-05 | 0.0049766 | missense | SPTAN1 | GRCh38.p7 | 9:128608919 | GCCGACCAGCTCATC[A/G]CTGCCGGCCATTATG | 6709 |
rs747798323 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616976 | GGTGTGGTGGCTCAC[A/G]CCTATAATCCCAACA | 6709 |
rs747830535 | snp | C/T | 0.00015159 | 0.00870472 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567019 | CCAAAATTCAAGAGC[C/T]CAAATGTTCTTACCC | 6709 |
rs747869001 | snp | A/C | 4.94271e-05 | 0.00497102 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578093 | GAAACATAATGTCTT[A/C]CTTTGGTTTTCCCTA | 6709 |
rs747871167 | snp | A/G | 1.69243e-05 | 0.00290893 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632980 | TCAGGAGGTGGGTGA[A/G]GAGGTGTCCTTTGGA | 6709 |
rs747907795 | snp | A/G | 3.62102e-05 | 0.00425486 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609601 | TAATAGCTGATATGT[A/G]TGTCCACATCAGTGT | 6709 |
rs747909190 | snp | A/G | 1.65622e-05 | 0.00287764 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591652 | ACTGGGGGCCGCAAG[A/G]GCTAGGCGTCCCATA | 6709 |
rs747912590 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627966 | TGTTTTCTTCCTTCT[C/T]TGGGCTTGTCATGTG | 6709 |
rs747920481 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610694 | TCAGTACCTTCTGTT[A/T]CTTTATGGATTCATA | 6709 |
rs747928279 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | SPTAN1 | GRCh38.p7 | 9:128575203 | TCCCTGAATAGGAAG[C/T]AATTGTTACTTCTGA | 6709 |
rs747954026 | snp | C/T | 3.50988e-05 | 0.00418905 | downstream-variant-500B, utr-variant-3-prime | SPTAN1, WDR34 | GRCh38.p7 | 9:128633720 | TCGGCACAGCGAAGG[C/T]TTGCACCCGCCTCCC | 6709 |
rs747954042 | snp | C/T | 1.67368e-05 | 0.00289277 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632277 | GACCAGCTGGACCAG[C/T]TGGGCATGCGCATGC | 6709 |
rs747955504 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596910 | CATGCCTGTAATCCC[A/G]GCACTTTGGGAGGCC | 6709 |
rs747986519 | snp | A/G | | | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128552063 | GGAAGAGACGCACTC[A/G]GGTGATCTCACCCTT | 6709 |
rs747994166 | snp | A/C | 4.94654e-05 | 0.00497295 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617942 | TTCGAGACAGAAGCA[A/C]CAGAAGAGCTACCTG | 6709 |
rs748011302 | snp | G/T | 0.000225759 | 0.0106221 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627338 | TGAAGGAGGGGCTGG[G/T]GTCACTGCCACAGCA | 6709 |
rs748019516 | snp | C/T | 1.69732e-05 | 0.00291313 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611698 | GGTTTGGAAAAAATT[C/T]TTTTGGTATTTTTAG | 6709 |
rs748045045 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583580 | TTCTCCAGTGTCCTT[A/C]TATCTCAAGGGGGTT | 6709 |
rs748059445 | snp | A/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128578153 | GACCTCACCAGCTGG[A/G]TGACTGAGATGAAAG | 6709 |
rs748076414 | snp | A/G | 0.000148245 | 0.00860815 | missense | SPTAN1 | GRCh38.p7 | 9:128607624 | TCATGTCTTGGATCA[A/G]TGGAATACGGGGGTT | 6709 |
rs748110014 | snp | C/T | 1.64754e-05 | 0.00287009 | missense | SPTAN1 | GRCh38.p7 | 9:128584835 | AGGGGAATGCCATGG[C/T]GGAGGAAGGTGAGTG | 6709 |
rs748113883 | snp | A/G | 9.90851e-05 | 0.00703795 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608282 | TAACGTCCAGGTGAG[A/G]CCTCTGGACCATGGA | 6709 |
rs748149636 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565708 | CCTTTTCTTTCTGTC[C/T]TGGGATAGACGACAG | 6709 |
rs748154034 | snp | C/T | 1.65081e-05 | 0.00287293 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632424 | CTAATTTCTGTTTTT[C/T]TTCCAGGAACACAAC | 6709 |
rs748161340 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622731 | TTCAATGTGACTTGT[A/T]GTATGGTTTATTTAT | 6709 |
rs748193081 | snp | C/T | 1.66835e-05 | 0.00288816 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128583232 | GGCAGCTCGTATGAA[C/T]GAGGTGATCAGTTTG | 6709 |
rs748212863 | snp | G/T | 1.64727e-05 | 0.00286986 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603613 | GCAGTGACCAGCTCC[G/T]CTGATCTCCCCTGGT | 6709 |
rs748214653 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588157 | CGCCCGCCACCACGC[C/T]CAGCTAATTTTTGTA | 6709 |
rs748232676 | snp | A/C | 1.65067e-05 | 0.00287282 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128566795 | GACATCCAGGAGAGG[A/C]GGCAGCAGGTCCTAG | 6709 |
rs748240922 | snp | C/T | 5.03647e-05 | 0.00501795 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628067 | CGGGCTGCACTTCCC[C/T]TCCCACCCTTCTCGT | 6709 |
rs748242562 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576468 | TTAACAGCCTCATGA[A/G]CATCTGAAATACCAA | 6709 |
rs748252362 | snp | C/T | 1.68878e-05 | 0.00290579 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613345 | GCTGAGTATACACCA[C/T]ACAGTAGCCTTTGCT | 6709 |
rs748252690 | snp | C/T | 4.94686e-05 | 0.00497311 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574845 | GAAGGGTTTGCTAAG[C/T]TTTACTCAAAGAAAA | 6709 |
rs748258817 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587914 | GCAGTGGCACAACCT[C/T]GGCTCACTGCAACCT | 6709 |
rs748281012 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622140 | TGCAAATAAACTTGC[A/G]TGAAACTAATTTCAG | 6709 |
rs748287344 | snp | C/T | 1.64953e-05 | 0.00287182 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128617700 | AACCGGCGTGCAGAA[C/T]CTGAGGAAGAAGCAC | 6709 |
rs748303045 | snp | C/T | 1.64732e-05 | 0.0028699 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608125 | CTGCCTCTTGCCCTC[C/T]TTAGCTGTTCCATCG | 6709 |
rs748317084 | snp | C/G/T | 3.32996e-05 | 0.00408031 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587568 | GGATGGGAGGCTTCA[C/G/T]CCCCTGCACAGTGCT | 6709 |
rs748332117 | snp | C/G | 3.31148e-05 | 0.00406894 | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633368 | CACCCCTCGCTGCTT[C/G]CCCTGCGTCGCCTTG | 6709 |
rs748338558 | snp | A/G | 1.64901e-05 | 0.00287137 | missense | SPTAN1 | GRCh38.p7 | 9:128583800 | TAGGAATAAAGCTTC[A/G]TGAAGCCAACCAGCA | 6709 |
rs748379097 | in-del | -/C | 2.32472e-05 | 0.00340926 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632091 | TGACTGAGCTGAGGG[-/C]CCCCGTCTGAGCATC | 6709 |
rs748383650 | in-del | -/AA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603733 | AAGCATGTCCTAAGT[-/AA]ACATCAGCACATTCA | 6709 |
rs748410014 | snp | A/G | 1.65436e-05 | 0.00287602 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594134 | CATCTACAGCTAACT[A/G]CCTTCCTTGTCCCTC | 6709 |
rs748421270 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631737 | GAGATTGAGGCAGGA[C/G]AATCACTTGAACCCG | 6709 |
rs748437388 | snp | G/T | 4.51518e-05 | 0.0047512 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628155 | AGCCTTCAAGCCAGG[G/T]GGAGCCGTCCTTGCC | 6709 |
rs748450616 | snp | A/G | 3.29554e-05 | 0.00405914 | missense | SPTAN1 | GRCh38.p7 | 9:128618971 | ACCCTGGTGGCCAGC[A/G]AAGATTATGGCGACA | 6709 |
rs748451019 | snp | A/G | 3.41166e-05 | 0.00413003 | downstream-variant-500B, missense | SPTAN1, WDR34 | GRCh38.p7 | 9:128633931 | TGGGTTTGCTTGATC[A/G]AAACTGTGGGTTTCT | 6709 |
rs748472114 | snp | A/G | 1.64901e-05 | 0.00287137 | missense | SPTAN1 | GRCh38.p7 | 9:128605425 | CGTGCAGATCAGCGC[A/G]AGGCAAAGTTGGGTG | 6709 |
rs748479231 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568160 | GTGGAACAGTAGTTG[A/G]GCCCATGGATTTTTT | 6709 |
rs748490066 | snp | A/G | 1.66827e-05 | 0.00288809 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128626576 | TGACTTCAACCAGCT[A/G]GCCGAGCTGGACCGC | 6709 |
rs748531242 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600691 | GTTTTGAGATGGAGT[A/G]TTGCCCTGTCACCCA | 6709 |
rs748540221 | snp | A/G | 1.70845e-05 | 0.00292267 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618153 | AACAAGTGGAAGGCC[A/G]GCACCCAAGGGCAGA | 6709 |
rs748547880 | in-del | -/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581076 | TAATCTGTGAGCAAA[-/G]CCTTGCCAGTGGTGG | 6709 |
rs748559698 | snp | C/T | 1.65141e-05 | 0.00287346 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605264 | GAGCATACCCCCTTA[C/T]TGCAAGCTCATTCAC | 6709 |
rs748606170 | snp | A/C | 1.64933e-05 | 0.00287165 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128585929 | GGAACCCATTGTGGG[A/C]AGCACTGACTATGGC | 6709 |
rs748615499 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128581815 | GACTTGGGAGATTCC[C/T]TGGATAGTGTGGAAG | 6709 |
rs748642362 | snp | A/C | 1.65162e-05 | 0.00287365 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632727 | CGAACAGGTAAATTA[A/C]TTAAGGCCAGGTGCT | 6709 |
rs748646482 | snp | A/C/G | 3.29458e-05 | 0.00405857 | missense | SPTAN1 | GRCh38.p7 | 9:128612144 | TGACCAGTGGCAGTT[A/C/G]TTGGTGCAAAAGTCA | 6709 |
rs748647375 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591175 | CATGCCATTCTCCTG[A/C]ATCAGCCTCCCGAGT | 6709 |
rs748698544 | snp | A/G | 3.29647e-05 | 0.00405971 | missense | SPTAN1 | GRCh38.p7 | 9:128594317 | ACAAGTGAGGAGGTC[A/G]GAGCAGACTTGGAGC | 6709 |
rs748724744 | snp | G/T | 1.64773e-05 | 0.00287026 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582583 | GGTTCTTCATGCTCC[G/T]CCTTTTTGGTACATG | 6709 |
rs748734080 | snp | C/G | 1.72946e-05 | 0.00294058 | downstream-variant-500B, intron-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128634014 | ATACGTGGAGTAAGA[C/G]AAACTCTAGAGACCA | 6709 |
rs748748920 | snp | C/T | 1.64768e-05 | 0.00287021 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607577 | CAGGTAATATAATAG[C/T]TATTTTTCTGGGGTG | 6709 |
rs748813503 | snp | C/T | 4.33924e-05 | 0.00465772 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626722 | CAGGAGCTGCTCGGC[C/T]TCCCAGAGCCCTCTC | 6709 |
rs748818790 | snp | G/T | 1.65181e-05 | 0.00287381 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584577 | AAAGGCTGTGCTATT[G/T]TAGCATAAAGGGGAT | 6709 |
rs748859810 | in-del | -/G | 1.64732e-05 | 0.0028699 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584699 | CATGGTTGGATAACT[-/G]GGGACTGGTGTCTGC | 6709 |
rs748879524 | snp | G/T | 6.60306e-05 | 0.00574551 | missense | SPTAN1 | GRCh38.p7 | 9:128566844 | AGGAACTCTCAACCC[G/T]TAGGCGTCAGAAGCT | 6709 |
rs748880239 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605651 | GAGCCGGAGACCAGC[C/G]TGGGCTACATGGCGA | 6709 |
rs748881611 | snp | A/G | 1.67391e-05 | 0.00289297 | missense | SPTAN1 | GRCh38.p7 | 9:128577497 | ATGCACGGCTCAATG[A/G]TTCATACAGGTGCAA | 6709 |
rs748889468 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571187 | CCCAGCTACTGGGGA[C/G]GCTGAGGTGGGAGGA | 6709 |
rs748891230 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587562 | AGTGGAGGATGGGAG[A/G]CTTCAGCCCCTGCAC | 6709 |
rs748942344 | snp | C/T | 1.6486e-05 | 0.00287102 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128613390 | TGCCAGGTGGAGGCC[C/T]TGCTGGCATCCGAAG | 6709 |
rs748964931 | in-del | -/TATA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570305 | CCTGTTTAGACAGCT[-/TATA]TATATATATATATAT | 6709 |
rs748991679 | in-del | -/AA | 0.00018121 | 0.00951695 | splice-donor-variant | SPTAN1 | GRCh38.p7 | 9:128600117 | CTCCCCGTGGAAGGT[-/AA]AAGAACTCCTTTGCA | 6709 |
rs749001794 | snp | C/T | 1.64762e-05 | 0.00287016 | missense | SPTAN1 | GRCh38.p7 | 9:128582706 | CAGCTGTTGAGCCGC[C/T]GCAATGCCCTTCACG | 6709 |
rs749009632 | snp | C/G | 3.31115e-05 | 0.00406874 | missense | SPTAN1 | GRCh38.p7 | 9:128621164 | CTACTCCAGGGCTTA[C/G]TGAAGAAACATGAAG | 6709 |
rs749088637 | snp | C/T | 1.65075e-05 | 0.00287289 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580877 | CTGCCTCGGAGGCAT[C/T]GGGGCTGACCTCATC | 6709 |
rs749094320 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579826 | TCCTTAAATATCCAG[A/G]GAACGCATTCACCAT | 6709 |
rs749113807 | snp | A/G | 5.11592e-05 | 0.00505737 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615875 | TAGAAGGCCCCTTAC[A/G]CCTGTAATAGTGGGC | 6709 |
rs749144327 | in-del | -/AGGTATGGGCCTCAGGAGGTGGGTGAAGAGGT | 3.3627e-05 | 0.00410029 | frameshift-variant | SPTAN1 | GRCh38.p7 | 9:128632953 | AGGAGGAGCTCTACC[lengthTooLong]AGGTATGGGCCTCAG | 6709 |
rs749166998 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575399 | TATGTTAACTTTTTA[A/G]TATATTCAGGATAAA | 6709 |
rs749218036 | snp | C/T | 1.64944e-05 | 0.00287175 | missense | SPTAN1 | GRCh38.p7 | 9:128609270 | GAGTCGTACAAGGAT[C/T]CCACCAACATCCAGG | 6709 |
rs749251486 | snp | C/G | 1.6473e-05 | 0.00286988 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128591551 | GAAATTGGACCCCGC[C/G]CAGTCAGCCTCCCGG | 6709 |
rs749252791 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563855 | ATTACCTAGGCTGTT[C/G]TCGAACTTCTGGGCT | 6709 |
rs749258451 | snp | C/T | 1.64819e-05 | 0.00287066 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612104 | GGCTCCCTTCTGTTC[C/T]CCAGGCCCGCCTGGC | 6709 |
rs749263783 | snp | C/T | 1.65269e-05 | 0.00287457 | missense | SPTAN1 | GRCh38.p7 | 9:128584481 | TTGAGGATGAGGAGA[C/T]GTGGATTCGAGAGAA | 6709 |
rs749280114 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576391 | AAAAAAAGAAATGTC[A/G]TCAGTCTAAAGCCAG | 6709 |
rs749280573 | snp | C/G | 1.64792e-05 | 0.00287042 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574825 | GACAAGGCACGTTTT[C/G]GGAAGAAGGGTTTGC | 6709 |
rs749286316 | snp | A/G | 2.07626e-05 | 0.00322194 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632108 | CCCGTCTGAGCATCT[A/G]TGCTCCCCACCCCTG | 6709 |
rs749296938 | snp | A/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128580999 | GTACGAGCAGTGCAT[A/G]GACCTGCAGCTCTTC | 6709 |
rs749333383 | snp | G/T | 3.29538e-05 | 0.00405904 | missense | SPTAN1 | GRCh38.p7 | 9:128607966 | ATCAAGCAGAAACTT[G/T]ATATTCTTGACCAGG | 6709 |
rs749336810 | snp | A/G | 1.64857e-05 | 0.00287099 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128585911 | ATCCTGGATGCGGGA[A/G]AAGGAACCCATTGTG | 6709 |
rs749366280 | snp | A/G | 3.29462e-05 | 0.00405857 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577114 | TGTGGATTAACTGGT[A/G]CCTTTGTTCTGTAGG | 6709 |
rs749366800 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630410 | TGGCCCAGCAGAGAC[C/G]CTTCACCCAGCCACC | 6709 |
rs749376164 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619942 | CTGGGCTGAGAGATC[C/T]ATCACACACTGGCAG | 6709 |
rs749388739 | snp | A/G | 1.64955e-05 | 0.00287184 | missense | SPTAN1 | GRCh38.p7 | 9:128632612 | AGGCTGAACCATCAG[A/G]AGTTCAAATCTTGCC | 6709 |
rs749391487 | snp | A/C | 1.64751e-05 | 0.00287007 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128618958 | CAATGAGAAAATGAC[A/C]CTGGTGGCCAGCGAA | 6709 |
rs749402652 | snp | G/T | 3.39582e-05 | 0.00412043 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579598 | TTTATTTTGTAAGAT[G/T]CTGGGCACAAATCAT | 6709 |
rs749406261 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613144 | GTGCATTTTGCCTTA[C/G]CTGTAGTATTTACTA | 6709 |
rs749408098 | snp | C/T | 1.64947e-05 | 0.00287177 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611887 | AGGGAGGAAGATGAC[C/T]ACCGTCACTGTCAAC | 6709 |
rs749417587 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631470 | CTCTGAAAAAAATTA[C/T]TTGGGCATGGTGGCC | 6709 |
rs749433827 | in-del | -/GG | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597199 | TTTTCTGTAGAGATA[-/GG]GGGGTCTGGTTATGT | 6709 |
rs749451493 | snp | A/C | 1.64871e-05 | 0.00287111 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625052 | ATGTTTTTCCTTTCT[A/C]ATCCATCTCCACTGA | 6709 |
rs749461128 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567870 | GATTCAAGTGATTCT[C/G]CTGCCTCAGCCTCCC | 6709 |
rs749484552 | snp | C/T | 0.000148707 | 0.00862158 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613377 | TTTGTGTTTTCATTG[C/T]CAGGTGGAGGCCCTG | 6709 |
rs749486029 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599155 | TTTCTTTTTTTTTGA[A/G]ACGGAGTCTCACTCT | 6709 |
rs749534578 | snp | C/G | 3.32105e-05 | 0.00407482 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583072 | CCCCCTTCTTTTATT[C/G]ACAGGATCCATCCAA | 6709 |
rs749543704 | snp | A/G | 1.64732e-05 | 0.0028699 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627990 | TCATGTGGGGGTCTC[A/G]TGCGCTTGCCCCTCG | 6709 |
rs749590351 | in-del | -/CTCC | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631938 | TCACATTGAAAGTCT[-/CTCC]CTCTATTGAGGTGGT | 6709 |
rs749595393 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625405 | GGACTGGGCACTGCA[A/G]GAGCACTCACTCAGT | 6709 |
rs749639256 | snp | A/G | 3.30557e-05 | 0.00406531 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581102 | GGTGGGAGAAGAAGG[A/G]CCTGTGTTTTGCCTC | 6709 |
rs749672064 | snp | C/T | 1.64912e-05 | 0.00287147 | stop-gained | SPTAN1 | GRCh38.p7 | 9:128588887 | CAGGAGAAGAGTCCC[C/T]GAGAGGTCACCATGA | 6709 |
rs749674291 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567078 | TATGACCTTGAGAGA[C/T]TGGACAAGAAGAATA | 6709 |
rs749747503 | snp | A/G | 1.64969e-05 | 0.00287196 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128576921 | GCAGAGGCAGGGGAA[A/G]CTCTTTGGGGCAGCA | 6709 |
rs749760692 | snp | A/G | 1.70067e-05 | 0.002916 | downstream-variant-500B, missense | SPTAN1, WDR34 | GRCh38.p7 | 9:128633919 | GGGCTTTCATCCTGG[A/G]TTTGCTTGATCAAAA | 6709 |
rs749763206 | snp | C/T | 5.08789e-05 | 0.0050435 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618144 | GCTCCCGGGAACAAG[C/T]GGAAGGCCAGCACCC | 6709 |
rs749768274 | snp | A/G | 5.62588e-05 | 0.00530342 | synonymous-codon, intron-variant | SPTAN1 | GRCh38.p7 | 9:128592983 | GCCCCCTCTGTGCAG[A/G]ACACGCATAACTAAG | 6709 |
rs749809951 | snp | A/G | 1.65141e-05 | 0.00287346 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605255 | TGTTCTGCAGAGCAT[A/G]CCCCCTTACTGCAAG | 6709 |
rs749835470 | snp | A/G | 4.94173e-05 | 0.00497053 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128581784 | TTCCTTTGGCAAGGC[A/G]TTCCTGTTGAATGAA | 6709 |
rs749878606 | in-del | -/AAAC | 1.70586e-05 | 0.00292045 | downstream-variant-500B, frameshift-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128633931 | GGGTTTGCTTGATCA[-/AAAC]AAACTGTGGGTTTCT | 6709 |
rs749896543 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566643 | TTGTCTCCTGGGTTT[A/G]TCTGATAATTATTTC | 6709 |
rs749921643 | snp | A/C | 3.29451e-05 | 0.00405851 | missense | SPTAN1 | GRCh38.p7 | 9:128591539 | TGCGTACGTGAAGAA[A/C]TTGGACCCCGCCCAG | 6709 |
rs749923214 | snp | C/T | 2.31795e-05 | 0.0034043 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604433 | GTGAGGGGTCAGCCC[C/T]GGGCTGGGAGAGGGA | 6709 |
rs750007543 | snp | A/G | 5.23876e-05 | 0.00511772 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128604337 | GCAGGAGCTGAATGA[A/G]CGCTGGCGGTCCCTA | 6709 |
rs750012433 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565051 | GGCTCACACCTGTAA[A/T]TCCAGCCCTTTGGGA | 6709 |
rs750014146 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576014 | CATTTTCTGGCCAGT[A/G]ATTAAGAGAAAGATA | 6709 |
rs750019133 | snp | C/G | 1.65674e-05 | 0.00287809 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608848 | CCACAGGCCCACCTT[C/G]ATCTCATGCCTTTGT | 6709 |
rs750031205 | snp | C/T | 1.84561e-05 | 0.00303772 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609341 | TGTTATTGAGTAGAT[C/T]TTGTTAAATAAAGCA | 6709 |
rs750048080 | snp | A/G | 1.65436e-05 | 0.00287602 | missense | SPTAN1 | GRCh38.p7 | 9:128575331 | GTGAACCAGTTTGCT[A/G]CCAAACTCATACAGG | 6709 |
rs750065393 | snp | C/T | 1.65206e-05 | 0.00287403 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591636 | AATCAGTAAGGATGA[C/T]ACTGGGGGCCGCAAG | 6709 |
rs750076377 | snp | A/G | 1.66435e-05 | 0.0028847 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632367 | AGCCCAGAGCAGGGG[A/G]AGGAAAAGACACAGT | 6709 |
rs750100416 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577626 | TATCACCTACAAATG[C/G]AAATCACTTCTTACC | 6709 |
rs750120519 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630997 | TACAAGCGTGAGCCA[C/G]CACATCTGGCCTAGT | 6709 |
rs750155023 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601459 | TGGCTAGGTGTTGTG[G/T]CTCACACCTGTAATC | 6709 |
rs750180930 | in-del | -/ATT | 6.58897e-05 | 0.00573938 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581750 | TCAAAGGAATAGGAC[-/ATT]ATTCTGAACACTTTG | 6709 |
rs750201178 | snp | C/T | 3.29457e-05 | 0.00405854 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612270 | GAGTGGTTCCTCTTC[C/T]TACCAGTGGGGGATT | 6709 |
rs750230911 | snp | C/T | 1.65446e-05 | 0.00287612 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619052 | TCTCTTGGCAACTGC[C/T]TGCTGGTCATCATTT | 6709 |
rs750246766 | in-del | -/ACAAAT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608484 | AAAAATATTATCAAA[-/ACAAAT]GGGATGGAAAACAAA | 6709 |
rs750256276 | in-del | -/ATG | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580428 | AACATTAGATAAATA[-/ATG]ATTTATATGATTTAT | 6709 |
rs750267810 | snp | C/T | 2.03238e-05 | 0.00318771 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579779 | GAGGAGCAAATTACA[C/T]CTTTCACTAAGTCTC | 6709 |
rs750280087 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614429 | AAACCCCGTTTCTAC[G/T]GAAATACAAAAAATT | 6709 |
rs750280372 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587510 | TCATTGTGCAACTGA[A/G]AAAGGCTGTTGAGGC | 6709 |
rs750290385 | snp | A/C | 1.64741e-05 | 0.00286998 | missense | SPTAN1 | GRCh38.p7 | 9:128594206 | GAACTGGGTGAGAAG[A/C]GTAAAGGCATGTTGG | 6709 |
rs750291281 | snp | C/T | 1.64876e-05 | 0.00287116 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612092 | TCATCTCTTTTTGGC[C/T]CCCTTCTGTTCCCCA | 6709 |
rs750291744 | snp | A/G | 8.37809e-05 | 0.00647174 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632222 | CATCCTGGACAACAA[A/G]TACACGGAGCACAGC | 6709 |
rs750293826 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602492 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCATCA | 6709 |
rs750322980 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606734 | CAGGTGATCCACCCA[C/T]CTCGGCCTCCCAAAG | 6709 |
rs750333664 | snp | A/C/T | 3.32051e-05 | 0.00407451 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625185 | CACCAAACAGGTCTG[A/C/T]CCTGGCCCCTTCACT | 6709 |
rs750346901 | snp | A/G | 2.82554e-05 | 0.00375858 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628129 | AGCCCATGGTCCCTG[A/G]TCCCCGATAGAGCCT | 6709 |
rs750347402 | in-del | -/C | 1.65321e-05 | 0.00287502 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632794 | CTCAGGCTCTTGCTT[-/C]CCCCCGCTCCTAGAG | 6709 |
rs750359826 | snp | A/G | 3.32928e-05 | 0.00407987 | missense | SPTAN1 | GRCh38.p7 | 9:128583218 | GCCAAGGATGAAGTG[A/G]CAGCTCGTATGAATG | 6709 |
rs750378015 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633409 | GCTCCTCTGTGTGCT[C/G]TCACTTTCCACTGTA | 6709 |
rs750388353 | snp | C/T | 0.000116072 | 0.00761725 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628052 | CCTTCCTGCCCAGGG[C/T]GGGCTGCACTTCCCC | 6709 |
rs750393039 | snp | A/G | 0.000132286 | 0.00813176 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587588 | TGCACAGTGCTCCAT[A/G]TGTGGTTTTGGTTTC | 6709 |
rs750399428 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128556634 | ATGAATCTTTTGCTT[G/T]CTTAAAGCTAAGTCC | 6709 |
rs750424658 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604545 | TTTATTTGTGACATG[A/G]GGTGGGTGCTCAGTA | 6709 |
rs750428546 | snp | C/T | 3.30611e-05 | 0.00406565 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632789 | TCCCTGCTCAGGCTC[C/T]TGCTTCCCCCGCTCC | 6709 |
rs750455967 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575387 | TCACAACATTATTAT[A/G]TTAACTTTTTAGTAT | 6709 |
rs750465466 | snp | C/T | 1.64738e-05 | 0.00286995 | missense | SPTAN1 | GRCh38.p7 | 9:128609198 | CTCCAACAGTTCAGC[C/T]GGGATGTGGATGAGA | 6709 |
rs750471165 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626116 | ACATGGGTGTGGCTG[G/T]CATCAATTAAAACCA | 6709 |
rs750506396 | snp | A/G | 1.64757e-05 | 0.00287012 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609084 | CTTCTCCACGGTAAG[A/G]TATGCTCATGTTGGA | 6709 |
rs750518161 | snp | A/C | 1.65329e-05 | 0.0028751 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128584392 | GGCTCGCTATGAGGC[A/C]CTCAAGGAGCCCATG | 6709 |
rs750521661 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613216 | AGAGTGTCTCAGGCC[A/G]GGCAGGCTGATTGGG | 6709 |
rs750533648 | in-del | -/TT/TTT/TTTT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594429 | ATTTGAGTCTCTTGA[-/TT/TTT/TTTT]TTTTTTTTTTTTTTT | 6709 |
rs750537498 | snp | A/C | 3.29652e-05 | 0.00405974 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630403 | GGGGCTCTGGCCCAG[A/C]AGAGACCCTTCACCC | 6709 |
rs750553315 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591872 | AGAATTTTTCTAATC[A/G]TTGCCATTTGCCTTT | 6709 |
rs750564748 | snp | G/T | | | missense | SPTAN1 | GRCh38.p7 | 9:128581792 | GCAAGGCGTTCCTGT[G/T]GAATGAAGACTTGGG | 6709 |
rs750595740 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627164 | CTTGACTGACCAGTC[A/G]CTTCCCTCCAGGTCC | 6709 |
rs750596137 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627801 | ATGCAGGGTCTGTGC[A/G]TTGGGTACTGATGTT | 6709 |
rs750603114 | snp | A/G | 1.64795e-05 | 0.00287045 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577003 | GTCTCAACCTGGAGG[A/G]GAGTTGTGAAGCACA | 6709 |
rs750606387 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563112 | TTTTAAGGACTTGAC[A/G]TCTGTTTTAAGAATA | 6709 |
rs750616250 | snp | G/T | 1.64825e-05 | 0.00287071 | missense | SPTAN1 | GRCh38.p7 | 9:128582494 | GCATTAGATGAATTT[G/T]CAACCAAGCTAATTC | 6709 |
rs750635508 | snp | A/G | 3.73274e-05 | 0.00431999 | missense | SPTAN1 | GRCh38.p7 | 9:128626640 | TACACCTGGTTTACC[A/G]TGGAGGCCCTGGAGG | 6709 |
rs750692902 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593218 | GCGGTGCAGCTGTGT[C/T]GGTCGATGACTGCTT | 6709 |
rs750705450 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588343 | TGAGATGGAGTTTCA[C/G]TCTTGTTGCCCAGGT | 6709 |
rs750706032 | snp | C/T | 1.65094e-05 | 0.00287305 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581902 | ATTACAGTAAGACCC[C/T]TTCTTGTCAGTGCTT | 6709 |
rs750714061 | snp | A/G | 1.68832e-05 | 0.00290539 | downstream-variant-500B, missense | SPTAN1, WDR34 | GRCh38.p7 | 9:128633896 | TGTTGAACTCCAGAC[A/G]GTAGACAGGGCTTTC | 6709 |
rs750735256 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619495 | TTGCTGGCACCAGGC[A/G]CCCTTGGCATGTGGC | 6709 |
rs750746952 | snp | A/G | 1.67206e-05 | 0.00289137 | missense | SPTAN1 | GRCh38.p7 | 9:128624461 | TTCAGTTCAACTGGA[A/G]GGCGGACGTGGTGGA | 6709 |
rs750748842 | snp | A/G | 1.64792e-05 | 0.00287042 | missense | SPTAN1 | GRCh38.p7 | 9:128615707 | ACCTCCCAAGTAAAG[A/G]ACAAGAGGGACACCA | 6709 |
rs750772716 | snp | A/C | 1.64751e-05 | 0.00287007 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600035 | CCAGGTGCTTTGTTT[A/C]ATGGTCAATTGCTTG | 6709 |
rs750773935 | snp | C/T | 1.6476e-05 | 0.00287014 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578087 | CCGCTGGAAACATAA[C/T]GTCTTCCTTTGGTTT | 6709 |
rs750784854 | snp | C/T | 1.65682e-05 | 0.00287817 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582871 | TACTGTTAGTGTTGC[C/T]ATGTAGCACTCGATT | 6709 |
rs750819513 | snp | C/T | 4.94173e-05 | 0.00497053 | synonymous-codon, intron-variant | SPTAN1 | GRCh38.p7 | 9:128627937 | CAGGACATACCTCCT[C/T]GATGGGTTAATATTG | 6709 |
rs750847756 | snp | A/G | 1.64779e-05 | 0.00287031 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128607914 | TGAGCAGTTTGGACA[A/G]CAGCTGTTGGCTCAC | 6709 |
rs750853937 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581182 | CTGAATCCATTGAAG[A/T]GGGGGAATTGAGCAA | 6709 |
rs750855679 | snp | G/T | | | missense | SPTAN1 | GRCh38.p7 | 9:128605413 | AGCCTGGGGAAACGT[G/T]CAGATCAGCGCAAGG | 6709 |
rs750894293 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585438 | ATAGAGTGCCTGCAC[A/G]TGCCAGTCTCAGTAA | 6709 |
rs750900657 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578077 | CCTGGAACCTCCGCT[A/G]GAAACATAATGTCTT | 6709 |
rs750904635 | snp | C/T | 4.9588e-05 | 0.00497911 | missense, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633255 | TCTCCCACATGAAGC[C/T]CTACGTGGACGGCAA | 6709 |
rs750909666 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629833 | CTGCAGGGTCGTGCT[C/T]TCATTCCCCCTAGAA | 6709 |
rs750917350 | snp | A/G | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554776 | CATAGCTCATCACTG[A/G]GGGCCACTTGACTGG | 6709 |
rs750918353 | snp | A/G | 1.648e-05 | 0.0028705 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600163 | GAGTTTTGCGAGATC[A/G]TGAAATATGTCCTTT | 6709 |
rs750918991 | in-del | -/TTG | 3.29489e-05 | 0.00405874 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599013 | TGCTGTGTGTGGATC[-/TTG]TTGAACATGAGAAGG | 6709 |
rs750958035 | in-del | -/A | 3.37225e-05 | 0.00410611 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613513 | GGCGGGCCAGGCCCG[-/A]AGTGCCTGGGACACA | 6709 |
rs750970258 | snp | A/G | 3.30437e-05 | 0.00406457 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568764 | CTCACTTCAAGGTCC[A/G]CCAACAGGGAAAGCT | 6709 |
rs750970364 | snp | A/G | 3.29891e-05 | 0.00406122 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128578239 | AGATAGACACCAAGA[A/G]CACAAGGTAATGGTA | 6709 |
rs750990425 | snp | C/T | 1.67225e-05 | 0.00289154 | intron-variant, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633182 | TGCAGCTGGCTCAGG[C/T]ACCAGGTGCCATCTC | 6709 |
rs751012803 | snp | C/T | 1.6522e-05 | 0.00287414 | missense | SPTAN1 | GRCh38.p7 | 9:128625168 | TCTGTGCAGACGCTC[C/T]TCACCAAACAGGTCT | 6709 |
rs751032951 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607015 | TGTCTATGGATTTGC[C/G]TCTTCTGGACATGTC | 6709 |
rs751040631 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603535 | CTTCTGCTTTCCTCC[C/T]TACCTAGTCTGCTCG | 6709 |
rs751051882 | in-del | -/G | 6.0596e-05 | 0.00550403 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628135 | TGGTCCCTGGTCCCC[-/G]ATAGAGCCTTCAAGC | 6709 |
rs751058174 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620516 | GAGGTCAGGAGTCCG[A/G]GACCAACCTGGCCAA | 6709 |
rs751083948 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575709 | CCACCAATGCATTAG[G/T]GCTCTTGCCTTCCTT | 6709 |
rs751095961 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588305 | CGGCCCTACTTTAAA[A/G]TGAGATTTTTTTTTT | 6709 |
rs751104914 | snp | C/T | 1.66092e-05 | 0.00288172 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128583199 | GATTGATGTCAACCA[C/T]TATGCCAAGGATGAA | 6709 |
rs751128580 | snp | C/G | 1.6476e-05 | 0.00287014 | missense | SPTAN1 | GRCh38.p7 | 9:128608034 | GATGATGCTGGATCA[C/G]TGCCTTGAACTGCAG | 6709 |
rs751171934 | snp | A/G | 1.65018e-05 | 0.00287239 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128617640 | CCATCTCTCATTCAG[A/G]GAGAAGAAGCTGCTG | 6709 |
rs751184113 | snp | A/G | 1.77852e-05 | 0.00298199 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604285 | CTGGGGGCATGACAG[A/G]AGAGGGAGTGCAGTG | 6709 |
rs751209815 | snp | G/T | 1.65059e-05 | 0.00287275 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128625786 | AACTTTTGACGCTGG[G/T]CTGCAGGCCTTCCAG | 6709 |
rs751209866 | in-del | -/TTCCT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128555620 | AAAATTTGCAAAGCC[-/TTCCT]TTTTTTTTTTTTTTT | 6709 |
rs751220762 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615416 | CCCCTCCTCCATTGC[A/T]TTTGTACTATCAGTG | 6709 |
rs751247659 | in-del | -/A | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583746 | TGTTGGCAGAAGGGT[-/A]AATGCTAAGCAGTAC | 6709 |
rs751291380 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630829 | CCTGCCTCAACCTCC[C/T]AAGTAGCTGGGATTA | 6709 |
rs751295099 | snp | A/G | 1.6904e-05 | 0.00290719 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128579729 | TGCCTCAGATGAAGT[A/G]AGGGAGAAGGTAAGA | 6709 |
rs751323441 | snp | A/G | 3.36344e-05 | 0.00410074 | downstream-variant-500B, stop-gained | SPTAN1, WDR34 | GRCh38.p7 | 9:128633875 | CCAAGAGCTGAGTCT[A/G]CTGGCTGTTGAACTC | 6709 |
rs751323903 | snp | A/G | 1.65274e-05 | 0.00287462 | missense, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633276 | TGGACGGCAAGGGCC[A/G]CGAGCTCCCCACCGC | 6709 |
rs751333951 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618860 | ATTTTCTTCCTGTCT[C/T]CTGTAATTAGGGGTC | 6709 |
rs751336135 | snp | C/G | 1.64846e-05 | 0.0028709 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611863 | ATGGCCCACCAGCTC[C/G]CGGTGCCCAGGGAGG | 6709 |
rs751337586 | snp | C/T | 1.64974e-05 | 0.00287201 | missense | SPTAN1 | GRCh38.p7 | 9:128626514 | GAAATCAAAGCTTTG[C/T]GCGAGGCCCACGACG | 6709 |
rs751346515 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578377 | CTCATCATGAGGATT[A/G]TGGTTGGTTTTGCCT | 6709 |
rs751409455 | snp | A/C/G | 6.5895e-05 | 0.00573967 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603639 | CTGGTTTTCTCCACT[A/C/G]TCTTCCTTCCCTGTC | 6709 |
rs751423380 | snp | C/G | 1.64784e-05 | 0.00287035 | missense | SPTAN1 | GRCh38.p7 | 9:128625877 | CAGTCCAAGGCCATC[C/G]AGGCCCGGCACGCCT | 6709 |
rs751426251 | snp | C/G | 1.66807e-05 | 0.00288792 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618116 | GCTGCCCGGTGAGTA[C/G]TCAGAGGCAGGAGCT | 6709 |
rs751444203 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568460 | ATGTTCACATAAAGG[C/G]TAATTTTCTGATAGC | 6709 |
rs751451527 | snp | A/G | 5.01811e-05 | 0.00500879 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585976 | CTGAGGTAACCAGGC[A/G]TGGGAAGCGTCTCAC | 6709 |
rs751473819 | snp | C/T | | | missense | SPTAN1 | GRCh38.p7 | 9:128566849 | CTCTCAACCCTTAGG[C/T]GTCAGAAGCTGGAAG | 6709 |
rs751477608 | snp | A/C/T | 4.94192e-05 | 0.00497067 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627977 | TTCTCTGGGCTTGTC[A/C/T]TGTGGGGGTCTCGTG | 6709 |
rs751517664 | snp | A/G | 1.65012e-05 | 0.00287234 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632565 | CGCCCTCGGCTTTGT[A/G]CTGCAGACACTTTGA | 6709 |
rs751532108 | snp | C/T | 1.65002e-05 | 0.00287225 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612069 | AGAGGGACGATTCTT[C/T]ATAGATTTCATCTCT | 6709 |
rs751535998 | in-del | -/GTGAGGCTCTGTTGCT | 5.91593e-05 | 0.0054384 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598525 | TGTCTCCATCTTGGA[-/GTGAGGCTCTGTTGCT]GTAAGGATGCAGCTT | 6709 |
rs751539530 | snp | C/T | 1.64792e-05 | 0.00287042 | missense | SPTAN1 | GRCh38.p7 | 9:128594176 | TTGAATTCCATCAGA[C/T]ATCATTCTCTGCTGG | 6709 |
rs751547120 | snp | A/C | 4.94425e-05 | 0.0049718 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576990 | CTTTGGGGAATGGGT[A/C]TCAACCTGGAGGGGA | 6709 |
rs751573290 | snp | C/G | 4.94727e-05 | 0.00497332 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583975 | TGCTCACCAGGTAGT[C/G]TGAACTGGGGGCTGT | 6709 |
rs751573694 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567729 | TTATCAAAAGCAAAG[A/C]CTGAATCTTATGGTA | 6709 |
rs751573713 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581710 | ATTTTGGCCAAAATA[C/T]CCTTTGCTTCACAGT | 6709 |
rs751584176 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628731 | CTGTATAGGCGGCCA[A/G]GGGAGAAATAGACCC | 6709 |
rs751593832 | snp | A/G | 3.30628e-05 | 0.00406575 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568748 | GTGGTTGCGTCTGAG[A/G]CTCACTTCAAGGTCC | 6709 |
rs751600620 | snp | A/T | 1.64955e-05 | 0.00287184 | missense | SPTAN1 | GRCh38.p7 | 9:128608949 | GCCAAGGGAGACATT[A/T]CTAGCCGGCGCAATG | 6709 |
rs751627937 | snp | A/G/T | 8.2485e-05 | 0.00642157 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605211 | CATCTTCTGTCTGGC[A/G/T]TTTTTGCCCCAGAAA | 6709 |
rs751640888 | snp | G/T | 3.29707e-05 | 0.00406008 | missense | SPTAN1 | GRCh38.p7 | 9:128615678 | ACAGCCTGATGACCA[G/T]CAGTGCCTTCGACAC | 6709 |
rs751671825 | snp | C/T | 1.64863e-05 | 0.00287104 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128588859 | GGAGCTGGTCTTGGC[C/T]CTCTACGACTATCAG | 6709 |
rs751721701 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591696 | CCACATGGGCCGAAG[C/T]TTAGGCGTGTCCTGA | 6709 |
rs751744467 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581749 | ATCAAAGGAATAGGA[C/T]ATTATTCTGAACACT | 6709 |
rs751759623 | snp | A/G | 9.95372e-05 | 0.00705398 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588765 | CTTAGATGACTCAGC[A/G]CGGACGTGTTTTTAC | 6709 |
rs751774320 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559351 | GGGGGACTTGCTCAG[A/G]TGGAACCTTTGCGAT | 6709 |
rs751775065 | snp | A/C | 8.29263e-05 | 0.00643865 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626350 | TGCGTCGGCACGTCC[A/C]GCCCTGGCGACTCCG | 6709 |
rs751784689 | snp | C/T | 1.64781e-05 | 0.00287033 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128605115 | ACATGATCTCGCCAG[C/T]GTCCAGGCCCTGCAA | 6709 |
rs751793555 | in-del | -/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574592 | GCTCCATAAGGTCTC[-/T]TAACTTGTCTAAACT | 6709 |
rs751794755 | snp | C/T | 3.29516e-05 | 0.00405891 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609075 | CCCCACTTCCTTCTC[C/T]ACGGTAAGATATGCT | 6709 |
rs751842367 | snp | A/G | 1.65217e-05 | 0.00287412 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584274 | GCTCTGTCCTTTTGC[A/G]TTCCCAGGACCGAAT | 6709 |
rs751852536 | in-del | -/TT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627545 | ATGTCCCTGCTGTAC[-/TT]TTAAGCCCTGGGGAG | 6709 |
rs751886085 | in-del | -/A | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606485 | GACATATATATATAT[-/A]TATTTTTTTTTTGGG | 6709 |
rs751897772 | snp | C/T | 5.67725e-05 | 0.00532757 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621287 | TGGTAAGACCTCCAT[C/T]GCCCACTGGGACACC | 6709 |
rs751909640 | snp | C/T | 1.64811e-05 | 0.00287059 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582686 | CACAGGGGATCCTTG[C/T]CTTTCAGCTGTTGAG | 6709 |
rs751916872 | snp | A/G | 5.1202e-05 | 0.00505948 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627509 | ACCAGGTGCCAGCCC[A/G]CTGGGGCCGGGGAGC | 6709 |
rs751917324 | snp | C/T | 1.64798e-05 | 0.00287047 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607553 | TTCCTGGGCAGAAGA[C/T]CTCCTTACCAGGTAA | 6709 |
rs751921459 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585357 | TCTTATCTGTGAAAC[A/G]GGGATGACAGCACCT | 6709 |
rs751936849 | in-del | -/TTTGTTTTGTTTTGTT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597638 | TTATAGCTTTTTTTG[-/TTTGTTTTGTTTTGTT]TTTGTTTTGTTTTGA | 6709 |
rs751993867 | snp | A/G | 1.72546e-05 | 0.00293718 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611673 | GAAAAGACATAACCT[A/G]GCAGGAACTGGTTTG | 6709 |
rs751996724 | snp | C/G | | | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128551241 | CTGCACAGGAATGAT[C/G]TGGGTGTTACTCCCA | 6709 |
rs752000519 | snp | C/T | 1.65072e-05 | 0.00287286 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632504 | GTTCAGCCTTACTCG[C/T]CCTGGCTGGGTGGGG | 6709 |
rs752006624 | snp | C/G | 0.000430015 | 0.0146568 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627175 | AGTCGCTTCCCTCCA[C/G]GTCCGCCTCTTCCTT | 6709 |
rs752007873 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572181 | CTTTATTTTTCCAAC[C/G]TGTACTTCATTCCTG | 6709 |
rs752009009 | snp | A/C | 1.65875e-05 | 0.00287984 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128624369 | TTCAAAGATGAAGGG[A/C]CTGAACGGGAAAGTG | 6709 |
rs752012743 | snp | A/T | 1.68315e-05 | 0.00290094 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632958 | GGAGCTCTACCAGGT[A/T]TGGGCCTCAGGAGGT | 6709 |
rs752055865 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597542 | AAGACAAAAAACTAC[A/G]GTTAATGAAGTAAAT | 6709 |
rs752072982 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573513 | CAAAGCTGGAGTTCA[A/G]TGGCACAATCTTGGC | 6709 |
rs752091618 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566113 | CCAGGGCGGAGCGCA[A/G]TGGTGCAATGATGGC | 6709 |
rs752102155 | snp | C/G | 1.64751e-05 | 0.00287007 | missense | SPTAN1 | GRCh38.p7 | 9:128582747 | GCGTCGCCGGGCCCA[C/G]CTAGCCGATTCTTTC | 6709 |
rs752113454 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599841 | TTCTTTATTCTCTCC[A/G]TTTCTTCTACTGGAT | 6709 |
rs752127383 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128598965 | TCTCTCCTTGTAGGA[A/G]GTGTATGGCATGATG | 6709 |
rs752146614 | snp | C/G | 1.67033e-05 | 0.00288987 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128577489 | AGAGAGACATGCACG[C/G]CTCAATGATTCATAC | 6709 |
rs752207276 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586563 | TATGTGTGCTTACAT[A/G]CATACTAACATACCA | 6709 |
rs752229124 | snp | C/T | 1.64887e-05 | 0.00287125 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128585827 | GAAAGCCAAAGCTTC[C/T]CAGCGTCGGCAGGAC | 6709 |
rs752281557 | snp | A/T | 5.43375e-05 | 0.00521208 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627615 | CAGAGGCAGCCTGGG[A/T]ATAAAGCTGGGCTGG | 6709 |
rs752294331 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613016 | TTGTTGGACATTGAG[G/T]TGTTCCCAGCCTTTT | 6709 |
rs752304112 | snp | C/T | 3.29707e-05 | 0.00406008 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611852 | GCTGTCAAGGTATGG[C/T]CCACCAGCTCCCGGT | 6709 |
rs752318149 | snp | A/G | 2.44556e-05 | 0.00349674 | synonymous-codon, intron-variant | SPTAN1 | GRCh38.p7 | 9:128593028 | ATCTCTGCGTATGAA[A/G]CAGGTGGAAGAACTG | 6709 |
rs752321315 | snp | C/T | 1.66194e-05 | 0.00288261 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585718 | TGTCAACGTAGTTTT[C/T]GTTATCCTCTTTCCC | 6709 |
rs752330996 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608771 | ATCCTGCCACCAGCT[A/G]GTTCTCAGTCACCCA | 6709 |
rs752335613 | snp | A/G | 1.65718e-05 | 0.00287848 | missense | SPTAN1 | GRCh38.p7 | 9:128583164 | CGAATTGATGCCTTG[A/G]AGAAAGCTGGCCAAA | 6709 |
rs752342805 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598507 | TGTGCAACAACAGGT[A/G]GGTGTCTCCATCTTG | 6709 |
rs752345517 | snp | A/G | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554108 | AAAAAAAGTGCTGCA[A/G]TAAAGGCCTCTGTGC | 6709 |
rs752347538 | snp | A/G | 0.000214159 | 0.0103457 | missense | SPTAN1 | GRCh38.p7 | 9:128608015 | AGGCCTGGGTTCAGC[A/G]CAGGATGATGCTGGA | 6709 |
rs752349221 | snp | A/G | 8.23703e-05 | 0.00641704 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600050 | CATGGTCAATTGCTT[A/G]GCTGCCTAAATTCCT | 6709 |
rs752364883 | snp | C/G/T | 3.29746e-05 | 0.00406035 | synonymous-codon, missense | SPTAN1 | GRCh38.p7 | 9:128618011 | GACACTGGCAAGAAG[C/G/T]TGTCCGATGACAACA | 6709 |
rs752387544 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567649 | AAATTTATAGTTATT[C/T]TGGAGTCAGATATCA | 6709 |
rs752391374 | snp | A/C/T | 8.23928e-05 | 0.00641801 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128605109 | TTATGGACATGATCT[A/C/T]GCCAGTGTCCAGGCC | 6709 |
rs752395675 | in-del | -/CC | 0.00021543 | 0.0103763 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626363 | CCAGCCCTGGCGACT[-/CC]GCCAACTCAGTCTCT | 6709 |
rs752424279 | snp | C/T | 1.654e-05 | 0.00287571 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584261 | CAAAGTAAAGTCTGC[C/T]CTGTCCTTTTGCATT | 6709 |
rs752428807 | in-del | -/AA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620725 | CTCCGTCTCAAAAAG[-/AA]AAAAAAAAGACATGA | 6709 |
rs752435451 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624716 | AAACAAAAGCCTGTA[A/G]ACGCTGCTGCACGCA | 6709 |
rs752480020 | snp | A/C | 3.30164e-05 | 0.00406289 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581074 | GGTAATCTGTGAGCA[A/C]AGCCTTGCCAGTGGT | 6709 |
rs752487210 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566246 | TATTTTTAGTAGAGA[C/T]GGTGTTTCACCTTGT | 6709 |
rs752548837 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561885 | ATTGGATCTATAATA[C/T]GTGCCAAGTCCTGAG | 6709 |
rs752549070 | in-del | -/TGATTCA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618426 | GAATCACAGAGTGGG[-/TGATTCA]TGATGTTCCATGGAC | 6709 |
rs752560514 | snp | C/G | 1.65031e-05 | 0.00287251 | missense | SPTAN1 | GRCh38.p7 | 9:128625927 | CCAGCTTCTGGCCAA[C/G]TCAGCCGCCCGCAAG | 6709 |
rs752569422 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128633038 | TGAGTCTGGGGTAAC[A/G]GGCCCTGCGCTGGGT | 6709 |
rs752570908 | snp | C/G | 1.66197e-05 | 0.00288263 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630218 | TGGTTTCCTTAAAAG[C/G]AATGTGAGGTTGCCA | 6709 |
rs752578570 | snp | A/G | 4.96512e-05 | 0.00498228 | missense | SPTAN1 | GRCh38.p7 | 9:128576872 | AGCAGGATGAAGTCA[A/G]TGCAGCCTGGCAGCG | 6709 |
rs752581960 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580305 | ATAAATAAATAAAAA[C/T]AAAATATGTATATAT | 6709 |
rs752581974 | snp | A/G | 3.30846e-05 | 0.00406709 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604986 | AGTGTCCTGTAATCA[A/G]GGCAGTTGTACTTGG | 6709 |
rs752585555 | snp | C/T | 3.42883e-05 | 0.0041404 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592956 | CCACTAATTCGTGCA[C/T]GCTTTTGCTGTGCCC | 6709 |
rs752604075 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579295 | GCCAGGGAGGGACTC[A/G]CCCTACCAGGTTCTA | 6709 |
rs752608993 | snp | A/G | 1.67756e-05 | 0.00289612 | downstream-variant-500B, missense | SPTAN1, WDR34 | GRCh38.p7 | 9:128633859 | TGGGCATCGCCCGCA[A/G]CCAAGAGCTGAGTCT | 6709 |
rs752613364 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560272 | GTATTTTAATAGAGA[C/T]GAGGTTCCACCGTGT | 6709 |
rs752668137 | snp | A/T | 1.64727e-05 | 0.00286986 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581744 | AGAAGATCAAAGGAA[A/T]AGGACATTATTCTGA | 6709 |
rs752674281 | snp | C/G | 1.65976e-05 | 0.00288072 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575367 | AGCAAAGTGCTGTAT[C/G]CTTCTCACAACATTA | 6709 |
rs752677999 | snp | A/G | 1.65291e-05 | 0.00287476 | missense | SPTAN1 | GRCh38.p7 | 9:128618068 | CGGCTGGCGCAGTTT[A/G]TGGAGCACTGGAAAG | 6709 |
rs752683769 | snp | C/T | 1.64857e-05 | 0.00287099 | missense | SPTAN1 | GRCh38.p7 | 9:128587649 | TGTCAGATCTCAGTG[C/T]CTACGGCAGCAGCAT | 6709 |
rs752702804 | snp | C/G/T | 3.35229e-05 | 0.00409396 | downstream-variant-500B, missense | SPTAN1, WDR34 | GRCh38.p7 | 9:128633785 | AGTCCAGGTCCTCAG[C/G/T]TTCCCGGGGCCCTTG | 6709 |
rs752710398 | snp | A/G | 1.66101e-05 | 0.0028818 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128577471 | GATCCGCACCTTGGC[A/G]GCAGAGAGACATGCA | 6709 |
rs752726334 | snp | A/G | 1.65389e-05 | 0.00287562 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632832 | TGTCTCCTTGCAAGA[A/G]TACATGGCTTTCATG | 6709 |
rs752726486 | snp | A/T | | | missense | SPTAN1 | GRCh38.p7 | 9:128575311 | ATGAAGAAAGAGTTA[A/T]TGAAGTGAACCAGTT | 6709 |
rs752734266 | in-del | -/A | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572928 | ACAGTGGTGGAAGTG[-/A]AATTGTGTGAGCATG | 6709 |
rs752791475 | snp | C/T | 1.6476e-05 | 0.00287014 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598947 | TAATAAAACTGGTTT[C/T]TCTCTCTCCTTGTAG | 6709 |
rs752797760 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602738 | CCTCCCAGGTTCAAG[C/T]GATTCTCATGCCTCA | 6709 |
rs752851473 | in-del | -/A | 1.65244e-05 | 0.00287436 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582464 | CAATGAAGAACTCTT[-/A]ATCTTCCTTCCTAGG | 6709 |
rs752865964 | snp | A/C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559334 | CAAGCTGGGCCCAAG[A/C/T]AGGGGGACTTGCTCA | 6709 |
rs752878085 | snp | C/T | 0.000132183 | 0.0081286 | synonymous-codon, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633295 | GCTCCCCACCGCGTT[C/T]GACTACGTGGAGTTC | 6709 |
rs752881438 | snp | A/G | 2.5562e-05 | 0.00357496 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598363 | TGACTTTGGCTTGCT[A/G]TTTTGGGTTTTAGTT | 6709 |
rs752891394 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603861 | CTGGAAGGAGCACAG[C/T]CTCAGTAATGCAGTG | 6709 |
rs752892851 | snp | A/T | 1.64757e-05 | 0.00287012 | missense | SPTAN1 | GRCh38.p7 | 9:128583944 | AGAAACATGCACTGC[A/T]AGAGGCAGATGTGGC | 6709 |
rs752934340 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579806 | TCTCTGAAAGCTATT[A/G]TTCATCCTTAAATAT | 6709 |
rs752936396 | snp | C/G | 2.61859e-05 | 0.00361832 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628236 | CGAAGGCCAGAGCTG[C/G]AGTCCAGAGGCCCTA | 6709 |
rs752954055 | snp | A/G | 3.31087e-05 | 0.00406857 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608870 | TGCCTTTGTTTTCTG[A/G]CAGGAAGAGAAGATT | 6709 |
rs752982738 | snp | C/T | 1.6591e-05 | 0.00288015 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588761 | TGTACTTAGATGACT[C/T]AGCGCGGACGTGTTT | 6709 |
rs753016149 | snp | A/G | 1.66427e-05 | 0.00288462 | missense | SPTAN1 | GRCh38.p7 | 9:128566966 | AATTATAAAGACCCA[A/G]CCAACTTGCAGGTAC | 6709 |
rs753021419 | snp | G/T | 8.39243e-05 | 0.00647728 | missense | SPTAN1 | GRCh38.p7 | 9:128632946 | CGTGACCAAGGAGGA[G/T]CTCTACCAGGTATGG | 6709 |
rs753034226 | snp | G/T | 4.95667e-05 | 0.00497804 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584536 | CAGAGGTCAGTCTGC[G/T]TCCCTCAGGTAGGAA | 6709 |
rs753042080 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627328 | AGCCCATCTGTGAAG[A/G]AGGGGCTGGTGTCAC | 6709 |
rs753047744 | snp | C/T | 2.85898e-05 | 0.00378075 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626696 | CATCAAGGTACACCT[C/T]CCGCTGCCCTCAGGA | 6709 |
rs753053330 | in-del | -/TAAG | 1.65002e-05 | 0.00287225 | frameshift-variant | SPTAN1 | GRCh38.p7 | 9:128632481 | ATTCAGCATGATGTT[-/TAAG]TAAGTGAGTTCAGCC | 6709 |
rs753055605 | snp | C/T | 1.64819e-05 | 0.00287066 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128609251 | ATTGCAAACAGCGAG[C/T]GATGAGTCGTACAAG | 6709 |
rs753063757 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628286 | AGCCACCGGGCTCTG[C/T]TGGGCTCTCACCTCT | 6709 |
rs753090619 | snp | C/T | 1.64825e-05 | 0.00287071 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582673 | AACACTAGAGACTCA[C/T]AGGGGATCCTTGTCT | 6709 |
rs753106083 | snp | C/T | 0.000181292 | 0.0095191 | missense | SPTAN1 | GRCh38.p7 | 9:128611790 | GTGGGGTTATCGACA[C/T]GGGCAACTCCCTCAT | 6709 |
rs753109393 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575158 | GCCATTGTTAACAAA[C/T]GTTGGTTGGTGACTC | 6709 |
rs753193156 | snp | A/G | 3.29489e-05 | 0.00405874 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577337 | GAGAATAGTTCTGAC[A/G]GAGTTCATTTCTAGG | 6709 |
rs753195760 | snp | C/G | 1.66371e-05 | 0.00288414 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621134 | CAGGCTCTCAATAGT[C/G]TGCCTTGGCTGCTTC | 6709 |
rs753197188 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608052 | CCTTGAACTGCAGGT[A/G]TGTGTGCTCCTGGTT | 6709 |
rs753236636 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128584752 | GGTCCAGAATCTGCT[A/G]AAGAAACATCAAGCC | 6709 |
rs753248165 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594381 | TCCAGAAGGTATGGG[C/T]AGTCTTCAGGCTCAG | 6709 |
rs753260036 | snp | C/T | | | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128611803 | CATGGGCAACTCCCT[C/T]ATTGAACGTGGAGCC | 6709 |
rs753283021 | snp | A/G | 1.64765e-05 | 0.00287019 | missense | SPTAN1 | GRCh38.p7 | 9:128582549 | ATGTGGCCACTCGCC[A/G]AGATGCTGTAAGTTT | 6709 |
rs753289161 | in-del | -/TTT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589576 | CCGCCGTGCCCGGCC[-/TTT]TTTTTTTTTTTTTTT | 6709 |
rs753299378 | in-del | -/TCTT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621538 | TCAAGCAATACAGTC[-/TCTT]TATAGGGACAGTAGA | 6709 |
rs753344059 | snp | A/G | | | intron-variant, synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128629164 | TGTCTATCAGTATGA[A/G]GTTGGGGATGATCTG | 6709 |
rs753364453 | snp | C/T | 3.29549e-05 | 0.00405911 | missense | SPTAN1 | GRCh38.p7 | 9:128582775 | TTCCATCTGCAGCAG[C/T]TTTTCCGTGATTCTG | 6709 |
rs753365170 | snp | A/T | 0.000403514 | 0.0141984 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592937 | TCATCCCTGTGGATT[A/T]ACCCCACTAATTCGT | 6709 |
rs753368707 | snp | G/T | 1.64738e-05 | 0.00286995 | missense | SPTAN1 | GRCh38.p7 | 9:128584811 | CACGCATCAAAGCAG[G/T]TACACAGAAGGGGAA | 6709 |
rs753371567 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597626 | TTGAACAGATCCTTA[C/T]AGCTTTTTTTGTTTG | 6709 |
rs753385129 | snp | A/G | 1.65773e-05 | 0.00287895 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575356 | TACAGGTAAATAGCA[A/G]AGTGCTGTATGCTTC | 6709 |
rs753397209 | snp | A/G | 0.000111093 | 0.00745211 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627531 | CCGGGGAGCAGCAGC[A/G]TGTCCCTGCTGTACT | 6709 |
rs753429285 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633558 | AGCTGCCCTCATTCC[A/G]ACTTCAGAAAATCGA | 6709 |
rs753436491 | snp | G/T | 3.29723e-05 | 0.00406018 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617983 | CCTCGTCCTTGCCTG[G/T]CAGGGTGTCCTGGAC | 6709 |
rs753454105 | snp | A/T | 1.66275e-05 | 0.00288331 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585707 | CTTCTGTGATGTGTC[A/T]ACGTAGTTTTTGTTA | 6709 |
rs753457145 | snp | C/T | 3.31505e-05 | 0.00407113 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584231 | ATTTTTCTCTGTATA[C/T]GATAAAACCACACCC | 6709 |
rs753469846 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612956 | TTTTTTTAATAATTG[C/T]GTAAGTTTATCATAG | 6709 |
rs753483573 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610520 | CCTCTGAAATGAAAC[A/G]TTTGATGCAGAATTC | 6709 |
rs753484447 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565510 | TCTCTTAGAAAGGCA[A/G]TCTTCAGATCTGATC | 6709 |
rs753496482 | snp | C/G | 8.23893e-05 | 0.00641778 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607739 | AGTAGCAAAGACGTG[C/G]CTGCTCTGCAGGGCC | 6709 |
rs753515426 | snp | A/G | 0.000345995 | 0.0131483 | missense | SPTAN1 | GRCh38.p7 | 9:128625832 | AACATCACTGCCCTC[A/G]AAGATCAGCTTCTCG | 6709 |
rs753517436 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621908 | GTGGGTCGGGAATTC[A/G]CCAGCAATCACTCAG | 6709 |
rs753523782 | snp | A/C | 1.65633e-05 | 0.00287774 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608857 | CACCTTGATCTCATG[A/C]CTTTGTTTTCTGACA | 6709 |
rs753568549 | snp | C/T | | | intron-variant, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633163 | AGGTCGGGTTTGAAG[C/T]GGGTGCAGCTGGCTC | 6709 |
rs753607645 | snp | C/G | 1.71755e-05 | 0.00293044 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587734 | GGGTTACTGGAGGGA[C/G]GCCTTGAAGGACTCA | 6709 |
rs753613973 | snp | A/G | 1.65053e-05 | 0.0028727 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128613461 | AAAGCATCAACTGCT[A/G]GAAGCAGATATATCT | 6709 |
rs753626416 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577791 | AGTATCACATGAAAT[A/G]TCTTATTAAAACCAG | 6709 |
rs753683495 | in-del | -/AG | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586316 | AATTTTATTTTTAGT[-/AG]AGACAGGGTCTCGCT | 6709 |
rs753691473 | snp | A/T | 1.65318e-05 | 0.002875 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128566899 | CTTTCAAAGAGATGC[A/T]GAAGAGCTGGAGAAA | 6709 |
rs753698426 | snp | A/G | 1.64844e-05 | 0.00287087 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128587632 | GAAACACGAAGCTTT[A/G]ATGTCAGATCTCAGT | 6709 |
rs753713040 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571760 | CTGAGTCTCAGAGAA[C/T]TTGAGTAACTTGCCC | 6709 |
rs753713488 | snp | A/G | 1.66983e-05 | 0.00288944 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617805 | CAGAGGTGTTTGAGT[A/G]GGCCCCAGGGGACAG | 6709 |
rs753713783 | snp | A/G | 0.000100947 | 0.00710376 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628139 | CCCTGGTCCCCGATA[A/G]AGCCTTCAAGCCAGG | 6709 |
rs753717192 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583596 | TATCTCAAGGGGGTT[A/G]GAATGCTTCCAGTTC | 6709 |
rs753735712 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559068 | TGAATGCTGACTGCA[C/G]TGGGAGCACATTGGT | 6709 |
rs753751750 | in-del | -/AAAG | 1.72077e-05 | 0.00293318 | downstream-variant-500B, intron-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128633987 | CTGCACGTCACCTGC[-/AAAG]AGAGACAGATACGTG | 6709 |
rs753753168 | snp | A/G | 1.64985e-05 | 0.0028721 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128581056 | CTGGATGAGCAAGCA[A/G]GAGGTAATCTGTGAG | 6709 |
rs753802828 | snp | C/T | 3.29538e-05 | 0.00405904 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128583912 | CAAAGATCTTACCAA[C/T]GTGCAGAACCTCCAG | 6709 |
rs753804658 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632385 | GAAAAGACACAGTCA[A/C]CTGCTGTGTGGAGGG | 6709 |
rs753811545 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558301 | AACGTTTGACTGCTG[C/T]GTTGCAGCATTTATA | 6709 |
rs753820910 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608487 | AAATATTATCAAAGG[G/T]ATGGAAAACAAATGT | 6709 |
rs753847805 | snp | C/G | 3.33128e-05 | 0.00408109 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621125 | AACACATAGCAGGCT[C/G]TCAATAGTGTGCCTT | 6709 |
rs753874178 | in-del | -/GAGATGGAG | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588329 | TTTTTTTTTTTTTTT[-/GAGATGGAG]TTTCACTCTTGTTGC | 6709 |
rs753881190 | snp | C/T | | | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128578206 | TGCCAGTGATGTGGC[C/T]GGGGCTGAAGCCCTG | 6709 |
rs753935525 | snp | A/G | 2.25365e-05 | 0.00335674 | missense | SPTAN1 | GRCh38.p7 | 9:128626674 | CCTGGAGGAACCTAC[A/G]GAAAATCATCAAGGT | 6709 |
rs753948032 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614737 | TGTGTCATGATCACA[C/T]CACCGCACTCTTGGA | 6709 |
rs753973885 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627244 | AGTGCTCTGAGCCGG[A/C]CTCATGTCTCCCAGC | 6709 |
rs753997982 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595520 | AACTTTTCTAAGCCT[A/G]AACTACAATAGATGT | 6709 |
rs754000036 | snp | A/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128581858 | AGCACGAAGACTTTG[A/G]GAAATCCCTTAGTGC | 6709 |
rs754015780 | snp | C/T | 1.70496e-05 | 0.00291967 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609318 | GTGTTGGTCTTGATG[C/T]AGCCTTATGTTATTG | 6709 |
rs754037849 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568960 | ATTGTAGATTCATGC[A/G]TACATGTCAGTTTGG | 6709 |
rs754042321 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615519 | GAGGTCCACATAACA[G/T]ACTTTGAGAATATCA | 6709 |
rs754042405 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601673 | TAAAAAGAAATTTTA[A/T]AAGTGTGTCCCCAGA | 6709 |
rs754044992 | snp | A/G | 1.68579e-05 | 0.00290321 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128621238 | TGTCTGCACCAATGG[A/G]CAAGACCTCATTAAG | 6709 |
rs754066930 | snp | C/T | 1.65891e-05 | 0.00287998 | missense | SPTAN1 | GRCh38.p7 | 9:128577460 | AACTGGGAGCAGATC[C/T]GCACCTTGGCGGCAG | 6709 |
rs754100852 | snp | C/G | 9.56755e-05 | 0.00691582 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594423 | TTTAAAGATTTGAGT[C/G]TCTTGATTTTTTTTT | 6709 |
rs754114979 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588363 | GTTGCCCAGGTTGAA[A/G]TGCATTGGCCTGATC | 6709 |
rs754135461 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600619 | ATATGGCTTAACCAG[A/G]ATGGGCCATCCCTGA | 6709 |
rs754156968 | snp | C/T | 0.000543465 | 0.0164753 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577298 | ACAAGCAGCTGATTC[C/T]GTAAATAAGTTACCA | 6709 |
rs754183499 | snp | C/T | 3.30224e-05 | 0.00406326 | missense | SPTAN1 | GRCh38.p7 | 9:128632706 | CAATCCTGGACACGG[C/T]GGATCCGAACAGGTA | 6709 |
rs754198819 | snp | A/G | 1.7354e-05 | 0.00294563 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588983 | GTTTGTTCCACGCTG[A/G]CACCTCCACGTATGC | 6709 |
rs754203830 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592553 | GCTGGGATTACAGGC[A/G]TGAGCCACCACGCCT | 6709 |
rs754211900 | snp | C/T | 1.64757e-05 | 0.00287012 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609093 | GGTAAGATATGCTCA[C/T]GTTGGATCTCATGGT | 6709 |
rs754212051 | snp | A/T | 8.25498e-05 | 0.00642402 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617622 | GACTGACTGTGCTGT[A/T]TCCCATCTCTCATTC | 6709 |
rs754228048 | snp | C/T | 3.30458e-05 | 0.0040647 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128584518 | CATTGCCGCATCTAC[C/T]AACAGAGGTCAGTCT | 6709 |
rs754254447 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605626 | AGGCAAGCGAATTGC[C/T]TGAACTCAGGAGCCG | 6709 |
rs754265582 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593828 | CCAGCAAGTTCATCT[C/T]GTCTCTCCACTGTAG | 6709 |
rs754276364 | snp | A/G | 8.24056e-05 | 0.00641841 | missense | SPTAN1 | GRCh38.p7 | 9:128625124 | AGGAGAACAGCTTGA[A/G]GACAGATGATTATGG | 6709 |
rs754297888 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564038 | AGCACTTTGGAAGAC[C/T]GGAGGTGGGAGGATC | 6709 |
rs754299854 | snp | A/G | 1.64836e-05 | 0.0028708 | missense | SPTAN1 | GRCh38.p7 | 9:128615810 | TGCACCAGTTCTTCC[A/G]GGACATGGATGACGA | 6709 |
rs754343710 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620396 | CAACCAAAAAGGCAT[C/G]GTCTGCAGTGCTTAA | 6709 |
rs754355974 | in-del | -/T | 0.000699464 | 0.018688 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627561 | TAAGCCCTGGGGAGC[-/T]TTCCAGCCCCAAGGA | 6709 |
rs754362594 | snp | A/G | 9.9149e-05 | 0.00704022 | missense, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633302 | ACCGCGTTCGACTAC[A/G]TGGAGTTCACCCGCT | 6709 |
rs754390638 | snp | A/T | 1.65356e-05 | 0.00287533 | missense | SPTAN1 | GRCh38.p7 | 9:128584421 | TGGTTGCCCGGAAGC[A/T]GAAGCTGGCCGATTC | 6709 |
rs754416258 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575532 | GGAAAATGCTTTTCA[A/G]TGTGTTGCCTTGGGC | 6709 |
rs754419719 | snp | C/G | 1.64765e-05 | 0.00287019 | missense | SPTAN1 | GRCh38.p7 | 9:128574744 | GAAAAAGGAATCAAA[C/G]TGCTGCAGGCCCAGA | 6709 |
rs754423586 | snp | A/C | 1.64923e-05 | 0.00287156 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630415 | CAGCAGAGACCCTTC[A/C]CCCAGCCACCCCCCA | 6709 |
rs754451902 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608490 | TATTATCAAAGGGAT[C/G]GAAAACAAATGTGTG | 6709 |
rs754477004 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128584821 | AGCAGTTACACAGAA[A/G]GGGAATGCCATGGTG | 6709 |
rs754477832 | snp | A/G | 6.65082e-05 | 0.00576625 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585708 | TTCTGTGATGTGTCA[A/G]CGTAGTTTTTGTTAT | 6709 |
rs754486480 | snp | A/T | 1.71484e-05 | 0.00292812 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611686 | CTAGCAGGAACTGGT[A/T]TGGAAAAAATTTTTT | 6709 |
rs754488910 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629239 | CTTTACTGATGCACT[C/G]TTGACATCCCCAGGC | 6709 |
rs754528571 | in-del | -/CCTA | 9.88321e-05 | 0.00702896 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603534 | CCTTCTGCTTTCCTC[-/CCTA]CCTAGTCTGCTCGTC | 6709 |
rs754586969 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566239 | TTTTTTGTATTTTTA[A/G]TAGAGACGGTGTTTC | 6709 |
rs754607337 | snp | A/C/G/T | 9.88613e-05 | 0.00703016 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128607920 | GTTTGGACAGCAGCT[A/C/G/T]TTGGCTCACGGACAC | 6709 |
rs754628228 | in-del | -/ATG | | | utr-variant-3-prime, downstream-variant-500B, cds-indel | SPTAN1, WDR34 | GRCh38.p7 | 9:128633645 | GTAAAAGACAAATAA[-/ATG]ATGACTTCCCCCAAA | 6709 |
rs754633182 | snp | C/G | 1.65888e-05 | 0.00287996 | missense | SPTAN1 | GRCh38.p7 | 9:128624391 | GGGAAAGTGTCAGAC[C/G]TGGAGAAAGCTGCAG | 6709 |
rs754641622 | snp | A/G | 1.64735e-05 | 0.00286993 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598996 | CCCAGGGTAAGTTTC[A/G]GGTGCTGTGTGTGGA | 6709 |
rs754695482 | snp | C/T | 4.94711e-05 | 0.00497324 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607810 | TGACGTCAGAGTGGG[C/T]ATCTGCTGCCAGTTA | 6709 |
rs754705047 | snp | A/G | 2.04275e-05 | 0.00319583 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627584 | CCCAAGGAGGTGGTG[A/G]TGCTTTGTGTAAAAC | 6709 |
rs754740906 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579143 | CACCAGGATATATAC[C/T]GTTAATGCAGTTCCA | 6709 |
rs754747878 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608608 | TTCCTATTATCAGGC[A/T]TAATTTTGTTCTGTT | 6709 |
rs754757547 | snp | C/G | 2.93432e-05 | 0.00383024 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604453 | TGGGAGAGGGAGAAA[C/G]AGGTGACTGCTGGTT | 6709 |
rs754781456 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565674 | GACAGGTTTCATTCC[G/T]AACTCTTAGCCTACT | 6709 |
rs754784949 | snp | A/G | 1.64781e-05 | 0.00287033 | missense | SPTAN1 | GRCh38.p7 | 9:128625839 | CTGCCCTCAAAGATC[A/G]GCTTCTCGCCGCCAA | 6709 |
rs754805906 | in-del | -/AA | | | downstream-variant-500B, intron-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128633987 | CTGCACGTCACCTGC[-/AA]AGAGAGACAGATACG | 6709 |
rs754818571 | snp | C/T | 1.65091e-05 | 0.00287303 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632417 | CTGTTCCCTAATTTC[C/T]GTTTTTCTTCCAGGA | 6709 |
rs754818642 | snp | C/G | 9.89136e-05 | 0.00703186 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128617992 | TGCCTGTCAGGGTGT[C/G]CTGGACACTGGCAAG | 6709 |
rs754829676 | snp | C/T | 1.65592e-05 | 0.00287738 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608861 | TTGATCTCATGCCTT[C/T]GTTTTCTGACAGGAA | 6709 |
rs754854820 | snp | A/G | 3.37661e-05 | 0.00410876 | downstream-variant-500B, missense | SPTAN1, WDR34 | GRCh38.p7 | 9:128633760 | CAGGCCGCCACCTCT[A/G]CTGCCAGGCAGTCCA | 6709 |
rs754860866 | snp | C/G | 1.6501e-05 | 0.00287232 | missense | SPTAN1 | GRCh38.p7 | 9:128632476 | CAAAGAATTCAGCAT[C/G]ATGTTTAAGTGAGTT | 6709 |
rs754868327 | in-del | -/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603278 | TCTGTCCAACTAGCT[-/G]CTAGAATTGTGGTTT | 6709 |
rs754888795 | snp | G/T | 1.65663e-05 | 0.002878 | missense | SPTAN1 | GRCh38.p7 | 9:128566937 | AGGAAAAACTTCAGA[G/T]TGCATCTGATGAGAA | 6709 |
rs754897168 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622416 | ACGATGCTTCTGCCT[C/T]AGCCTCCCTAGTAGC | 6709 |
rs754910706 | snp | C/G | 3.29707e-05 | 0.00406008 | missense | SPTAN1 | GRCh38.p7 | 9:128625912 | CATGAAGAGGTGGAG[C/G]CAGCTTCTGGCCAAC | 6709 |
rs754912001 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621999 | ACACACACATCATGA[A/G]TAAGATTTCTCATCA | 6709 |
rs754916401 | snp | A/G | 3.30038e-05 | 0.00406212 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581062 | GAGCAAGCAGGAGGT[A/G]ATCTGTGAGCAAAGC | 6709 |
rs754940960 | snp | A/C/G | 3.31089e-05 | 0.00406861 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591647 | ATGACACTGGGGGCC[A/C/G]CAAGGGCTAGGCGTC | 6709 |
rs754942248 | snp | G/T | 2.5903e-05 | 0.00359873 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598354 | TGTCTCCTTTGACTT[G/T]GGCTTGCTATTTTGG | 6709 |
rs754990249 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589067 | TCAAAGACATGAGTT[C/T]CCTCACCAATCCCCC | 6709 |
rs755016797 | snp | A/G | 1.74099e-05 | 0.00295037 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586017 | AGTGGAACAGGGCTT[A/G]TACTGAGAAGGAAGT | 6709 |
rs755038076 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587885 | GAGTCTCACTCCGTC[A/G]CCTAGGCTGGAGTGC | 6709 |
rs755046868 | snp | A/G | 1.64757e-05 | 0.00287012 | missense | SPTAN1 | GRCh38.p7 | 9:128615765 | GCATGGCGGCCTCCC[A/G]GCGAGCCAAGCTGAA | 6709 |
rs755073572 | snp | C/G | 1.64735e-05 | 0.00286993 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577316 | AAATAAGTTACCAAG[C/G]GTCAGGAGAATAGTT | 6709 |
rs755081860 | snp | C/T | 1.65135e-05 | 0.00287341 | missense | SPTAN1 | GRCh38.p7 | 9:128632712 | TGGACACGGTGGATC[C/T]GAACAGGTAAATTAA | 6709 |
rs755104724 | snp | C/G | 1.6473e-05 | 0.00286988 | missense | SPTAN1 | GRCh38.p7 | 9:128594266 | CGTGAAGCGAATGAA[C/G]TACAGCAATGGATCA | 6709 |
rs755106605 | in-del | -/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588664 | AGTTCTTGGATCAGA[-/T]TTTATTGGTAGCTTC | 6709 |
rs755110850 | snp | A/T | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128553745 | TAGATCCTAAAATAT[A/T]TAAGCCCTTTGTTCT | 6709 |
rs755130187 | snp | A/G | 1.65045e-05 | 0.00287263 | missense | SPTAN1 | GRCh38.p7 | 9:128608271 | GACAAAGCGATTAAC[A/G]TCCAGGTGAGGCCTC | 6709 |
rs755137553 | snp | C/T | 3.29587e-05 | 0.00405934 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128582523 | TCAGAACAACCACTA[C/T]GCAATGGAAGATGTG | 6709 |
rs755140657 | snp | A/G | 3.29679e-05 | 0.00405991 | missense | SPTAN1 | GRCh38.p7 | 9:128587633 | AAACACGAAGCTTTG[A/G]TGTCAGATCTCAGTG | 6709 |
rs755147540 | snp | A/G | 1.72746e-05 | 0.00293888 | downstream-variant-500B, intron-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128634006 | AGAGACAGATACGTG[A/G]AGTAAGAGAAACTCT | 6709 |
rs755161447 | snp | A/T | 3.29451e-05 | 0.00405851 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577124 | CTGGTGCCTTTGTTC[A/T]GTAGGGATGTGGATG | 6709 |
rs755165878 | snp | A/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128578207 | GCCAGTGATGTGGCT[A/G]GGGCTGAAGCCCTGC | 6709 |
rs755166792 | snp | C/T | 1.65449e-05 | 0.00287614 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128613476 | GGAAGCAGATATATC[C/T]GCCCATGAGGTAAGC | 6709 |
rs755181773 | snp | C/G | 3.49803e-05 | 0.00418198 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628141 | CTGGTCCCCGATAGA[C/G]CCTTCAAGCCAGGGG | 6709 |
rs755220170 | snp | C/G | 1.69513e-05 | 0.00291125 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613331 | GAATTTTCCAGAATG[C/G]TGAGTATACACCACA | 6709 |
rs755232081 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582894 | ACTCGATTAGTAAGC[C/T]AAACACAGCTCTCAC | 6709 |
rs755265765 | snp | A/C | 1.65138e-05 | 0.00287343 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128566749 | TCAGAAAATGGACCC[A/C]AGTGGGGTCAAAGTG | 6709 |
rs755266481 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593874 | GTTACTGTGCTAAGC[A/G]CTTGGTTTCAGTCCC | 6709 |
rs755269821 | snp | C/G | 1.67657e-05 | 0.00289527 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628064 | GGGCGGGCTGCACTT[C/G]CCCTCCCACCCTTCT | 6709 |
rs755273355 | snp | A/G | 1.64991e-05 | 0.00287215 | missense | SPTAN1 | GRCh38.p7 | 9:128626517 | ATCAAAGCTTTGCGC[A/G]AGGCCCACGACGCCT | 6709 |
rs755356541 | snp | C/G | 1.64749e-05 | 0.00287005 | missense | SPTAN1 | GRCh38.p7 | 9:128581870 | TTGAGAAATCCCTTA[C/G]TGCCCAGGAGGAAAA | 6709 |
rs755362291 | in-del | -/TCACTATGTTGGCCAGGCTAGTCTC | 1.65233e-05 | 0.00287426 | frameshift-variant | SPTAN1 | GRCh38.p7 | 9:128617730 | AAGCGGCTGGAAGCA[-/TCACTATGTTGGCCAGGCTAGTCTC]GAACTGGCTGCGCAT | 6709 |
rs755376100 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564122 | CTACAAAAAAAATTT[A/G]AAAATTAGCCAGTCA | 6709 |
rs755394501 | snp | G/T | 3.29511e-05 | 0.00405887 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609098 | GATATGCTCATGTTG[G/T]ATCTCATGGTTTCAC | 6709 |
rs755431637 | snp | C/G | 1.65086e-05 | 0.00287298 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574645 | AGAGCCAGTTGTGAT[C/G]TGATTAAAACTCTGA | 6709 |
rs755434212 | snp | C/T | 3.29516e-05 | 0.00405891 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128618959 | AATGAGAAAATGACC[C/T]TGGTGGCCAGCGAAG | 6709 |
rs755436331 | snp | A/G | 2.34844e-05 | 0.00342661 | missense | SPTAN1 | GRCh38.p7 | 9:128626679 | AGGAACCTACAGAAA[A/G]TCATCAAGGTACACC | 6709 |
rs755450955 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618724 | TCCTGATCTCGTGAT[C/T]TGCCCGCCTCGGCCT | 6709 |
rs755502313 | snp | A/G | 1.65225e-05 | 0.00287419 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584529 | CTACCAACAGAGGTC[A/G]GTCTGCTTCCCTCAG | 6709 |
rs755525111 | snp | C/G | 3.30415e-05 | 0.00406444 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584566 | ATCAACTTGGGAAAG[C/G]CTGTGCTATTGTAGC | 6709 |
rs755534131 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592142 | GGAAATATCCAGGAA[A/T]TACATTCCCACTAGA | 6709 |
rs755556784 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593133 | GAAGGCCTTTGTCCA[C/T]CCAGAAAGATGAGGT | 6709 |
rs755559513 | snp | C/T | 1.68371e-05 | 0.00290143 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632189 | CGAGGACCTGGGGGC[C/T]GCCATGGAGGAGGCC | 6709 |
rs755570414 | in-del | -/TG | 0.000170783 | 0.00923916 | downstream-variant-500B, frameshift-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128633936 | TTGCTTGATCAAAAC[-/TG]TGGGTTTCTGGGAGC | 6709 |
rs755597469 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565402 | TGGAAAAACAATAAT[A/G]CAACAAAAATACATG | 6709 |
rs755612920 | snp | A/G | 1.64776e-05 | 0.00287028 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128609242 | CAGTGAAAAATTGCA[A/G]ACAGCGAGTGATGAG | 6709 |
rs755615190 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128591545 | CGTGAAGAAATTGGA[C/T]CCCGCCCAGTCAGCC | 6709 |
rs755632323 | snp | A/G | 1.66452e-05 | 0.00288484 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617787 | GCCTTCTGGCCAAGA[A/G]GGCAGAGGTGTTTGA | 6709 |
rs755637148 | snp | C/T | 1.65444e-05 | 0.00287609 | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633342 | TGAACTGAGCCACTC[C/T]CTGGGTCACCCACCC | 6709 |
rs755647836 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575172 | ATGTTGGTTGGTGAC[C/T]CTGGCTCTCTTATGG | 6709 |
rs755657649 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567500 | TTTTGCCATGTTGGC[C/T]AGGCTGGTCTTGAAC | 6709 |
rs755709175 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597618 | GATACCTGTTGAACA[G/T]ATCCTTATAGCTTTT | 6709 |
rs755714453 | snp | A/G | | | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128551515 | AATCCTAGCTCTTCC[A/G]ATTGGTAGCTGCCTG | 6709 |
rs755726052 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577663 | CTCTCTGTTTGGAGA[C/T]TGGCAACTGTATCAT | 6709 |
rs755740619 | snp | A/G | 6.89192e-05 | 0.00586982 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611677 | AGACATAACCTAGCA[A/G]GAACTGGTTTGGAAA | 6709 |
rs755742062 | snp | C/T | 3.29538e-05 | 0.00405904 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574819 | ATCAATGACAAGGCA[C/T]GTTTTGGGAAGAAGG | 6709 |
rs755756880 | snp | C/G | 1.64768e-05 | 0.00287021 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582578 | TTGTAGGTTCTTCAT[C/G]CTCCTCCTTTTTGGT | 6709 |
rs755764317 | snp | A/G | 0.000476304 | 0.0154248 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627180 | CTTCCCTCCAGGTCC[A/G]CCTCTTCCTTGAAGC | 6709 |
rs755810489 | snp | A/G | 1.66358e-05 | 0.00288402 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632369 | CCCAGAGCAGGGGGA[A/G]GAAAAGACACAGTCA | 6709 |
rs755830467 | snp | A/G | 3.8384e-05 | 0.0043807 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609354 | ATTTTGTTAAATAAA[A/G]CATTTATAAAACAAT | 6709 |
rs755841718 | snp | A/C/T | 1.67323e-05 | 0.00289239 | missense, synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632273 | GTGGGACCAGCTGGA[A/C/T]CAGCTGGGCATGCGC | 6709 |
rs755854403 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565164 | AAAAATTAGCTGGGC[A/G]TGGTGGTGCAGGCCT | 6709 |
rs755854784 | snp | C/T | 4.10635e-05 | 0.00453101 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626718 | CCCTCAGGAGCTGCT[C/T]GGCCTCCCAGAGCCC | 6709 |
rs755915287 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620770 | TTCTGAGATGTGTTC[A/G]AGTTAAACCTTAAAA | 6709 |
rs755933560 | snp | C/T | 1.64852e-05 | 0.00287094 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128587623 | TCTACTGAAGAAACA[C/T]GAAGCTTTGATGTCA | 6709 |
rs755936007 | in-del | -/AAG | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601583 | TAAAAATGTTTTAAA[-/AAG]AAGAAGAAAAAAAGT | 6709 |
rs755941670 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612271 | AGTGGTTCCTCTTCC[C/T]ACCAGTGGGGGATTT | 6709 |
rs755945299 | snp | A/G | 1.70023e-05 | 0.00291563 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586000 | GTCTCACCTGCCAGG[A/G]AAGTGGAACAGGGCT | 6709 |
rs755962640 | snp | C/G | 1.648e-05 | 0.0028705 | missense | SPTAN1 | GRCh38.p7 | 9:128625827 | TTGCCAACATCACTG[C/G]CCTCAAAGATCAGCT | 6709 |
rs755993933 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557292 | TTGCTGAAAGAATGG[C/T]AATCCCAATGCTTTG | 6709 |
rs756006714 | snp | A/G | 1.64901e-05 | 0.00287137 | missense | SPTAN1 | GRCh38.p7 | 9:128617674 | GGCTCAGAGGACTAC[A/G]GCCGGGACCTAACCG | 6709 |
rs756009905 | snp | A/C | 1.65143e-05 | 0.00287348 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583332 | TTGGGGAACTAAATA[A/C]CCCTTTCTATTAAGT | 6709 |
rs756019238 | in-del | -/T | 1.65485e-05 | 0.00287645 | frameshift-variant | SPTAN1 | GRCh38.p7 | 9:128632855 | TTTCATGATCAGCCG[-/T]CGAAACTGAGAACGT | 6709 |
rs756058913 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628134 | ATGGTCCCTGGTCCC[C/T]GATAGAGCCTTCAAG | 6709 |
rs756081844 | snp | C/T | 4.24511e-05 | 0.00460693 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579783 | AGCAAATTACACCTT[C/T]CACTAAGTCTCTGAA | 6709 |
rs756084170 | snp | A/G | 1.64874e-05 | 0.00287113 | missense | SPTAN1 | GRCh38.p7 | 9:128605396 | TAAACCAGGCCTGGA[A/G]CAGCCTGGGGAAACG | 6709 |
rs756086104 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627250 | CTGAGCCGGCCTCAT[A/G]TCTCCCAGCCTCCTC | 6709 |
rs756096724 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586789 | CTCTTACCACTCTTC[A/C]CAAAAACTAGAATGA | 6709 |
rs756099218 | snp | C/T | 3.49516e-05 | 0.00418026 | missense | SPTAN1 | GRCh38.p7 | 9:128604338 | CAGGAGCTGAATGAG[C/T]GCTGGCGGTCCCTAC | 6709 |
rs756176825 | snp | A/T | 1.64972e-05 | 0.00287199 | missense | SPTAN1 | GRCh38.p7 | 9:128608265 | GACTTTGACAAAGCG[A/T]TTAACGTCCAGGTGA | 6709 |
rs756177348 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | SPTAN1 | GRCh38.p7 | 9:128576916 | GCTCTGCAGAGGCAG[A/G]GGAAGCTCTTTGGGG | 6709 |
rs756189269 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128603563 | TCGTCTGATGGTTCA[C/T]ACCGTGGCCACCTTT | 6709 |
rs756215461 | snp | A/G | 1.65364e-05 | 0.0028754 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581911 | AGACCCCTTCTTGTC[A/G]GTGCTTTCAAATGAC | 6709 |
rs756233569 | in-del | -/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577038 | ATGTGCTGGTGAGCT[-/G]TCGAGGCTGACTAGG | 6709 |
rs756236236 | snp | A/G | 1.68952e-05 | 0.00290642 | downstream-variant-500B, missense | SPTAN1, WDR34 | GRCh38.p7 | 9:128633899 | TGAACTCCAGACAGT[A/G]GACAGGGCTTTCATC | 6709 |
rs756241253 | snp | C/T | 3.29734e-05 | 0.00406025 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612094 | ATCTCTTTTTGGCTC[C/T]CTTCTGTTCCCCAGG | 6709 |
rs756242826 | snp | A/C | 1.6513e-05 | 0.00287336 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605250 | TCTTCTGTTCTGCAG[A/C]GCATACCCCCTTACT | 6709 |
rs756290749 | snp | C/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128575343 | GCTGCCAAACTCATA[C/G]AGGTAAATAGCAAAG | 6709 |
rs756296483 | snp | A/G | 1.64727e-05 | 0.00286986 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577107 | TCATTGCTGTGGATT[A/G]ACTGGTGCCTTTGTT | 6709 |
rs756311537 | snp | G/T | 1.64727e-05 | 0.00286986 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581767 | TATTCTGAACACTTT[G/T]TTTCCTTTGGCAAGG | 6709 |
rs756318195 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600260 | TTTCTTTCTGAATCT[C/G]TTAACTCTAAAATGT | 6709 |
rs756329176 | snp | A/G | 4.94205e-05 | 0.0049707 | missense | SPTAN1 | GRCh38.p7 | 9:128618924 | TTGTAGCCAATGTGG[A/G]AGAGGAAGAAGCCTG | 6709 |
rs756342577 | snp | C/T | 1.65053e-05 | 0.0028727 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632696 | GAGTTCGAGGCAATC[C/T]TGGACACGGTGGATC | 6709 |
rs756354801 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625257 | GCGTCTTTCACTGAG[A/G]CATTTATCTTCTGTT | 6709 |
rs756370704 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593349 | CTGAAGGCCTGTTCT[A/G]TAGTTTTCCTTAGTA | 6709 |
rs756378105 | snp | C/T | 4.94556e-05 | 0.00497246 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128588865 | GGTCTTGGCTCTCTA[C/T]GACTATCAGGAGAAG | 6709 |
rs756409693 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626306 | CGCCTCTGATTCCCA[G/T]GAACCACCCCGCACC | 6709 |
rs756431715 | snp | A/G | 1.64909e-05 | 0.00287144 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128568795 | TCAGAAGCATCAAGC[A/G]TTTGAAGCTGAAGTG | 6709 |
rs756434171 | snp | A/T | 1.64955e-05 | 0.00287184 | missense | SPTAN1 | GRCh38.p7 | 9:128632608 | TGGCAGGCTGAACCA[A/T]CAGGAGTTCAAATCT | 6709 |
rs756468298 | snp | A/G | 1.64746e-05 | 0.00287002 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600043 | TTTGTTTCATGGTCA[A/G]TTGCTTGGCTGCCTA | 6709 |
rs756497209 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591923 | AATTGGATTTTCAGA[A/T]ACTCTACGCCCCTAC | 6709 |
rs756506424 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563195 | CTGAGGCATGTGTAT[C/T]ACTTGAGTCCAGGAG | 6709 |
rs756509408 | in-del | -/C | 1.65526e-05 | 0.00287681 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599084 | ATCAGAATTGCTGTT[-/C]CTGAACCTCAGATGC | 6709 |
rs756542362 | snp | A/G | 1.64833e-05 | 0.00287078 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630406 | GCTCTGGCCCAGCAG[A/G]GACCCTTCACCCAGC | 6709 |
rs756550173 | snp | A/G | 0.000215498 | 0.010378 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626359 | ACGTCCAGCCCTGGC[A/G]ACTCCGCCAACTCAG | 6709 |
rs756557495 | snp | A/G | 1.69117e-05 | 0.00290785 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632975 | GGGCCTCAGGAGGTG[A/G]GTGAAGAGGTGTCCT | 6709 |
rs756560952 | snp | A/G | 1.64779e-05 | 0.00287031 | missense | SPTAN1 | GRCh38.p7 | 9:128615719 | AAGGACAAGAGGGAC[A/G]CCATCAACGGGCGCT | 6709 |
rs756562877 | in-del | -/GACT | 1.65143e-05 | 0.00287348 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617607 | GCAGGGAGGTGCAGA[-/GACT]GACTGTGCTGTTTCC | 6709 |
rs756590509 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619537 | AGTCTCTGCCTGTCT[G/T]CACGTAGCCATCTTC | 6709 |
rs756619034 | snp | C/T | 4.94246e-05 | 0.0049709 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609085 | TTCTCCACGGTAAGA[C/T]ATGCTCATGTTGGAT | 6709 |
rs756627870 | snp | C/T | 1.64914e-05 | 0.00287149 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568946 | CATCTGGGTGGAGCA[C/T]TGTAGATTCATGCAT | 6709 |
rs756640376 | snp | C/T | 1.64732e-05 | 0.0028699 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630280 | TGAGCTCTCGGCCAG[C/T]TGGGAGCAGGCCCCT | 6709 |
rs756673120 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604107 | TCAGAGAGGATGCCT[A/G]GGTCAGGTGTTTGTG | 6709 |
rs756685826 | snp | A/C | 4.95119e-05 | 0.00497529 | missense | SPTAN1 | GRCh38.p7 | 9:128584310 | GCATCACCATTCAGG[A/C]CCGCCAGTTCCAAGA | 6709 |
rs756687144 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591451 | GAGAAGGAATTTACT[C/T]TCAGTTCTCCCTCTT | 6709 |
rs756721547 | snp | G/T | 1.76646e-05 | 0.00297186 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604298 | AGGAGAGGGAGTGCA[G/T]TGGAGCTGATGTTTT | 6709 |
rs756748057 | snp | G/T | 1.65263e-05 | 0.00287452 | missense | SPTAN1 | GRCh38.p7 | 9:128625169 | CTGTGCAGACGCTCC[G/T]CACCAAACAGGTCTG | 6709 |
rs756767736 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607106 | TACAGCTGTGAGAAA[C/G]TGGATCAAATGTATG | 6709 |
rs756768219 | snp | A/G | 1.66161e-05 | 0.00288232 | missense | SPTAN1 | GRCh38.p7 | 9:128583203 | GATGTCAACCACTAT[A/G]CCAAGGATGAAGTGG | 6709 |
rs756769947 | in-del | -/TAAAT | 6.60557e-05 | 0.0057466 | splice-donor-variant | SPTAN1 | GRCh38.p7 | 9:128632720 | GTGGATCCGAACAGG[-/TAAAT]TAATTAAGGCCAGGT | 6709 |
rs756784077 | snp | A/C/G | 3.63876e-05 | 0.00426529 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579753 | GGTAAGAGAAGAGAA[A/C/G]TGGAGCTTTTGAGGA | 6709 |
rs756791394 | in-del | -/T | 1.67649e-05 | 0.0028952 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630201 | CCAGTTGCAGTTAGG[-/T]TTGGTTTCCTTAAAA | 6709 |
rs756794652 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588341 | TTTGAGATGGAGTTT[C/T]ACTCTTGTTGCCCAG | 6709 |
rs756798259 | snp | C/T | 1.65263e-05 | 0.00287452 | synonymous-codon, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633277 | GGACGGCAAGGGCCG[C/T]GAGCTCCCCACCGCG | 6709 |
rs756812781 | snp | A/G | 1.66015e-05 | 0.00288105 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617768 | CTATTCAGGTAAGGA[A/G]GCCGCCTTCTGGCCA | 6709 |
rs756822433 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594000 | TCTCTCAGGCTGTGG[C/T]GTGGGTACTTGGGAT | 6709 |
rs756859299 | snp | A/C | 0.000115313 | 0.0075923 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608100 | TTGCTGAAGGGCCTC[A/C]TTTTCTCACCTGCCT | 6709 |
rs756871934 | snp | A/G | 1.65636e-05 | 0.00287776 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578292 | AAGATTTTAGCTTAT[A/G]ATGCACCAGTTTATC | 6709 |
rs756886883 | snp | A/G | 1.6534e-05 | 0.00287519 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128584440 | GCTGGCCGATTCTCT[A/G]CGGTTGCAGCAGCTC | 6709 |
rs756887523 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598884 | TATCTCCTGTGTTTC[C/T]AGGTTTGGCCATAAT | 6709 |
rs756887707 | snp | A/C | 1.64868e-05 | 0.00287109 | stop-gained | SPTAN1 | GRCh38.p7 | 9:128609259 | CAGCGAGTGATGAGT[A/C]GTACAAGGATCCCAC | 6709 |
rs756893011 | snp | A/G | 3.29451e-05 | 0.00405851 | missense | SPTAN1 | GRCh38.p7 | 9:128591531 | GTGCCGGCTGCGTAC[A/G]TGAAGAAATTGGACC | 6709 |
rs756896679 | snp | C/T | 1.65293e-05 | 0.00287479 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128575321 | AGTTAATGAAGTGAA[C/T]CAGTTTGCTGCCAAA | 6709 |
rs756912451 | snp | A/C | 1.67925e-05 | 0.00289758 | missense | SPTAN1 | GRCh38.p7 | 9:128632200 | GGGCCGCCATGGAGG[A/C]GGCCCTCATCCTGGA | 6709 |
rs756977702 | snp | A/G | 1.65004e-05 | 0.00287227 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128617643 | TCTCTCATTCAGGGA[A/G]AAGAAGCTGCTGGTG | 6709 |
rs756980032 | snp | C/T | 1.64749e-05 | 0.00287005 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128574800 | TGAGGACGTGATGGA[C/T]TGGATCAATGACAAG | 6709 |
rs757000395 | snp | G/T | 1.65302e-05 | 0.00287486 | missense, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633323 | TTCACCCGCTCGCTT[G/T]TCGTGAACTGAGCCA | 6709 |
rs757022404 | snp | A/G | 1.64857e-05 | 0.00287099 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128585845 | GCGTCGGCAGGACCT[A/G]GAGGACTCTCTGCAG | 6709 |
rs757036070 | snp | C/T | 1.66023e-05 | 0.00288113 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585733 | TGTTATCCTCTTTCC[C/T]TACCCATCTTCCAGG | 6709 |
rs757043214 | snp | A/G | 1.64808e-05 | 0.00287057 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576994 | GGGGAATGGGTCTCA[A/G]CCTGGAGGGGAGTTG | 6709 |
rs757045012 | snp | C/T | 1.64977e-05 | 0.00287203 | missense | SPTAN1 | GRCh38.p7 | 9:128632573 | GCTTTGTGCTGCAGA[C/T]ACTTTGACAAGGACA | 6709 |
rs757049204 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630251 | CATTGCTCTCTCTGA[A/G]AGAAGGTTCATTCTG | 6709 |
rs757053083 | in-del | -/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589394 | CCTGCGTTCACCCCA[-/T]TCTCCTGCCTCAGCC | 6709 |
rs757064772 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586694 | ACATAGATGTACTTG[G/T]TTTTTTACTGGTTAT | 6709 |
rs757093848 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578496 | AGCTCTGGCGAGATA[A/G]AAGTGCTACTACTTG | 6709 |
rs757109566 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | SPTAN1 | GRCh38.p7 | 9:128612194 | TGAAAGAAGCCAACA[A/G]GCAGCAGAACTTCAA | 6709 |
rs757121963 | snp | A/G | 1.73936e-05 | 0.00294898 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624524 | CGGAAGAGCCTTCCC[A/G]GAGCTGCTCTTTGTC | 6709 |
rs757122103 | snp | C/T | 1.65015e-05 | 0.00287237 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628039 | ATCCCGGGATGGGCC[C/T]TCCTGCCCAGGGCGG | 6709 |
rs757140291 | snp | A/G | 8.38919e-05 | 0.00647603 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585982 | TAACCAGGCGTGGGA[A/G]GCGTCTCACCTGCCA | 6709 |
rs757162652 | snp | A/G | 3.30049e-05 | 0.00406219 | missense | SPTAN1 | GRCh38.p7 | 9:128632687 | CCTGACCCTGAGTTC[A/G]AGGCAATCCTGGACA | 6709 |
rs757178508 | snp | A/C | 0.000115661 | 0.00760377 | missense | SPTAN1 | GRCh38.p7 | 9:128625946 | GCCGCCCGCAAGAAG[A/C]AGCTTCTGGAGGCTC | 6709 |
rs757217441 | snp | A/G | 1.65926e-05 | 0.00288028 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582888 | TGTAGCACTCGATTA[A/G]TAAGCTAAACACAGC | 6709 |
rs757218211 | in-del | CTGATCTTGG/TCTTCCGATCT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588373 | TTGAAGTGCATTGGC[CTGATCTTGG/TCTTCCGATCT]CTCACCGCAACCTCC | 6709 |
rs757222917 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603648 | TCCACTATCTTCCTT[C/G]CCTGTCTACAGCAGA | 6709 |
rs757235715 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629858 | CTAGAATGGGGCTCC[C/G]TCCCTCAGGAACCTT | 6709 |
rs757274632 | snp | C/G | 1.6477e-05 | 0.00287024 | missense | SPTAN1 | GRCh38.p7 | 9:128607943 | ACGGACACTATGCCA[C/G]CCCTGAGATCAAGCA | 6709 |
rs757276587 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613159 | GCTGTAGTATTTACT[A/G]TGAATAGACTCTGGA | 6709 |
rs757335986 | in-del | -/A | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571124 | AGACCTCGTCTCTAC[-/A]AAAAAAAATTTAAAA | 6709 |
rs757354191 | snp | A/C | 1.65119e-05 | 0.00287327 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128625939 | CAACTCAGCCGCCCG[A/C]AAGAAGAAGCTTCTG | 6709 |
rs757363973 | snp | C/T | 4.95143e-05 | 0.00497541 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632526 | TGGGTGGGGGGTGTT[C/T]GGCAGCAGGGCTGCC | 6709 |
rs757364107 | in-del | -/A | 0.000693029 | 0.018602 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574651 | AGTTGTGATCTGATT[-/A]AAACTCTGATTTGAA | 6709 |
rs757364140 | snp | C/T | 1.6495e-05 | 0.0028718 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128608951 | CAAGGGAGACATTTC[C/T]AGCCGGCGCAATGAG | 6709 |
rs757365265 | snp | C/T | 1.65102e-05 | 0.00287312 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128584284 | TTTGCATTCCCAGGA[C/T]CGAATTGATGGCATC | 6709 |
rs757423491 | snp | C/T | 1.65318e-05 | 0.002875 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568749 | TGGTTGCGTCTGAGG[C/T]TCACTTCAAGGTCCG | 6709 |
rs757430734 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580599 | GAGTCCCTACTCCAT[C/T]TATACTCCATTAAAC | 6709 |
rs757432512 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595177 | TACAGTGGCTCGATC[G/T]CAGCTCACTGCAACT | 6709 |
rs757444230 | in-del | -/A | 0.000120797 | 0.00777071 | downstream-variant-500B, intron-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128634000 | CAAAGAGAGACAGAT[-/A]ACGTGGAGTAAGAGA | 6709 |
rs757448779 | snp | A/G | 3.2994e-05 | 0.00406152 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605228 | TTTTGCCCCAGAAAG[A/G]GCAGAGTCTTCTGTT | 6709 |
rs757450107 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560758 | GGTGCTGTGGCTCAC[A/G]TCTGTAATCCCAGCA | 6709 |
rs757453262 | snp | C/T | 1.64855e-05 | 0.00287097 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128588862 | GCTGGTCTTGGCTCT[C/T]TACGACTATCAGGAG | 6709 |
rs757455339 | snp | A/G | 1.64904e-05 | 0.00287139 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583977 | CTCACCAGGTAGTGT[A/G]AACTGGGGGCTGTGG | 6709 |
rs757456517 | in-del | -/CTCTAG | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574977 | TCTCTAGGTGTATGT[-/CTCTAG]GCTATTCTGTAACTC | 6709 |
rs757470089 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605258 | TCTGCAGAGCATACC[C/T]CCTTACTGCAAGCTC | 6709 |
rs757474026 | snp | A/G | 1.65831e-05 | 0.00287945 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626356 | GGCACGTCCAGCCCT[A/G]GCGACTCCGCCAACT | 6709 |
rs757485409 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622146 | TAAACTTGCGTGAAA[C/T]TAATTTCAGCTACAG | 6709 |
rs757496950 | snp | A/G | 1.6473e-05 | 0.00286988 | missense | SPTAN1 | GRCh38.p7 | 9:128598975 | TAGGAAGTGTATGGC[A/G]TGATGCCCAGGGTAA | 6709 |
rs757504801 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602920 | GGATTACAGGCGTGA[A/G]CCAGCATGCCTAGCC | 6709 |
rs757514658 | snp | C/G | 1.68156e-05 | 0.00289957 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618129 | TAGTCAGAGGCAGGA[C/G]CTCCCGGGAACAAGT | 6709 |
rs757550644 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572358 | TCCCTGCCCACTCAC[A/G]CTCTCAAATAATAGT | 6709 |
rs757552510 | snp | A/G | 5.70641e-05 | 0.00534123 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621288 | GGTAAGACCTCCATC[A/G]CCCACTGGGACACCC | 6709 |
rs757578154 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128582750 | TCGCCGGGCCCAGCT[A/G]GCCGATTCTTTCCAT | 6709 |
rs757586939 | snp | A/C/G | 9.88642e-05 | 0.00703022 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607736 | CTGAGTAGCAAAGAC[A/C/G]TGGCTGCTCTGCAGG | 6709 |
rs757621519 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559029 | GTTTTTTGGTGTCTC[C/T]TGTAATTGCACAAAT | 6709 |
rs757646933 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573465 | CTTTTCTACTTTTTT[A/G]TTTTTCCCGAGATGG | 6709 |
rs757657944 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577054 | TCGAGGCTGACTAGG[A/C]CTTGGTCCCATGGGG | 6709 |
rs757663569 | snp | A/G | 1.866e-05 | 0.00305445 | missense | SPTAN1 | GRCh38.p7 | 9:128598409 | TTAAAGGACCTGAAG[A/G]CCAATGAGTCACGGT | 6709 |
rs757669740 | snp | A/G | 1.6477e-05 | 0.00287024 | missense | SPTAN1 | GRCh38.p7 | 9:128582701 | TCTTTCAGCTGTTGA[A/G]CCGCCGCAATGCCCT | 6709 |
rs757700590 | snp | A/G | 3.35003e-05 | 0.00409256 | intron-variant, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633168 | GGGTTTGAAGTGGGT[A/G]CAGCTGGCTCAGGCA | 6709 |
rs757712954 | in-del | -/C | 1.65926e-05 | 0.00288028 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582888 | GTAGCACTCGATTAG[-/C]TAAGCTAAACACAGC | 6709 |
rs757714696 | snp | A/G | 1.65211e-05 | 0.00287407 | missense | SPTAN1 | GRCh38.p7 | 9:128608907 | CTGCAGGCCTTTGCC[A/G]ACCAGCTCATCGCTG | 6709 |
rs757734927 | snp | C/T | 0.000131852 | 0.00811842 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128615688 | GACCAGCAGTGCCTT[C/T]GACACCTCCCAAGTA | 6709 |
rs757748474 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584209 | GAATGGAAAAAAGAC[C/T]TTATCAATTTTTCTC | 6709 |
rs757766253 | in-del | -/CT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598531 | CATCTTGGAGTGAGG[-/CT]CTGTTGCTGTAAGGA | 6709 |
rs757829826 | snp | C/T | 3.31824e-05 | 0.00407309 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588766 | TTAGATGACTCAGCG[C/T]GGACGTGTTTTTACC | 6709 |
rs757881199 | snp | A/G | 1.65847e-05 | 0.0028796 | missense | SPTAN1 | GRCh38.p7 | 9:128624374 | AGATGAAGGGCCTGA[A/G]CGGGAAAGTGTCAGA | 6709 |
rs757916963 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586583 | CTAACATACCAACAT[A/G]CACACATACATATAT | 6709 |
rs757950995 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611419 | AGGCTGCAGTGAGCT[A/G]AGATTACGCCACTGC | 6709 |
rs758017157 | snp | C/T | 1.64836e-05 | 0.0028708 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128615814 | CCAGTTCTTCCGGGA[C/T]ATGGATGACGAGGAG | 6709 |
rs758019827 | snp | A/G | 8.24463e-05 | 0.00642 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128582801 | TTCTGATGAGCTCAA[A/G]AGTTGGGTCAATGAG | 6709 |
rs758023451 | snp | C/T | 1.64999e-05 | 0.00287222 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128588898 | TCCCCGAGAGGTCAC[C/T]ATGAAGAAGGGAGAT | 6709 |
rs758034806 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585529 | GATATCTGCTTCTTA[C/G]AGTCTAGATAGAGGT | 6709 |
rs758075445 | in-del | -/CCCATAG | 2.0969e-05 | 0.00323791 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628109 | GAGTGTGTGCCTTGC[-/CCCATAG]CCCATGGTCCCTGGT | 6709 |
rs758078340 | snp | C/G | 0.000413247 | 0.0143685 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578269 | ATCTCTAGAATCTTC[C/G]AGAAGTGAAGATTTT | 6709 |
rs758082477 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612274 | GGTTCCTCTTCCTAC[C/T]AGTGGGGGATTTCTA | 6709 |
rs758102864 | snp | C/T | 1.66302e-05 | 0.00288355 | intron-variant, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633204 | TGCCATCTCTTACCC[C/T]ACAGAACCTGACCCG | 6709 |
rs758109367 | snp | C/T | 1.64746e-05 | 0.00287002 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600056 | CAATTGCTTGGCTGC[C/T]TAAATTCCTCTTTCT | 6709 |
rs758124433 | snp | C/T | 8.857e-05 | 0.00665411 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630130 | TTCCCATCTCTAAAA[C/T]GGGAGAAATGCTCCC | 6709 |
rs758127988 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612042 | TTAGAAGTTCTCAAA[C/T]TGAGCTTTAGGAGAG | 6709 |
rs758128817 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567713 | AGAGACTTGGTAAAT[A/C]TTATCAAAAGCAAAG | 6709 |
rs758133621 | snp | A/G | 1.64762e-05 | 0.00287016 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128608019 | CTGGGTTCAGCGCAG[A/G]ATGATGCTGGATCAG | 6709 |
rs758145570 | snp | C/G | 3.23546e-05 | 0.00402197 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592966 | GTGCATGCTTTTGCT[C/G]TGCCCCCTCTGTGCA | 6709 |
rs758146178 | snp | C/G | 1.64727e-05 | 0.00286986 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581746 | AAGATCAAAGGAATA[C/G]GACATTATTCTGAAC | 6709 |
rs758152378 | snp | C/T | 9.96396e-05 | 0.00705761 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575371 | AAGTGCTGTATGCTT[C/T]TCACAACATTATTAT | 6709 |
rs758200512 | snp | C/T | 0.000333426 | 0.0129074 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627634 | AAGCTGGGCTGGCAA[C/T]GCCTGGTCGGGCTCT | 6709 |
rs758224715 | snp | C/T | 1.64836e-05 | 0.0028708 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611854 | TGTCAAGGTATGGCC[C/T]ACCAGCTCCCGGTGC | 6709 |
rs758240689 | in-del | -/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574079 | ACTTTTCCACCAAGA[-/T]TTTCCTGTTGTGCCT | 6709 |
rs758242330 | snp | A/G | 1.65091e-05 | 0.00287303 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581076 | TAATCTGTGAGCAAA[A/G]CCTTGCCAGTGGTGG | 6709 |
rs758250566 | snp | A/C | 8.71103e-05 | 0.00659906 | downstream-variant-500B, utr-variant-3-prime | SPTAN1, WDR34 | GRCh38.p7 | 9:128633725 | ACAGCGAAGGCTTGC[A/C]CCCGCCTCCCGGGAC | 6709 |
rs758304958 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598781 | ACTAATGGTAATTTC[A/G]TAAGTTCCTCAAAGA | 6709 |
rs758341534 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603867 | GGAGCACAGTCTCAG[A/T]AATGCAGTGAGCGGC | 6709 |
rs758342554 | snp | A/G | 1.65307e-05 | 0.0028749 | missense | SPTAN1 | GRCh38.p7 | 9:128576884 | TCAATGCAGCCTGGC[A/G]GCGGCTGAAGGGCCT | 6709 |
rs758356697 | snp | A/G | 1.65056e-05 | 0.00287272 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632519 | CCCTGGCTGGGTGGG[A/G]GGTGTTCGGCAGCAG | 6709 |
rs758379487 | snp | C/T | 4.96948e-05 | 0.00498447 | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633384 | CCCTGCGTCGCCTTG[C/T]TGCATGTCCGCTCCT | 6709 |
rs758392226 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610724 | AAAAACCATATCAGG[C/T]GCCCAGGATCAGGAG | 6709 |
rs758392650 | snp | G/T | 1.66158e-05 | 0.0028823 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585723 | ACGTAGTTTTTGTTA[G/T]CCTCTTTCCCTACCC | 6709 |
rs758401244 | in-del | -/ATCTC | 4.97146e-05 | 0.00498546 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566713 | TGCCTATTGGTACTT[-/ATCTC]AGCGCATTTTGTCAT | 6709 |
rs758404011 | snp | C/G | 1.65809e-05 | 0.00287926 | missense | SPTAN1 | GRCh38.p7 | 9:128611722 | TTTTTAGAGCAAGCA[C/G]CAGAAGCACCAGGCT | 6709 |
rs758405090 | snp | C/T | 1.67928e-05 | 0.0028976 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632949 | GACCAAGGAGGAGCT[C/T]TACCAGGTATGGGCC | 6709 |
rs758436409 | in-del | -/AT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606475 | TTTTTCCCTAGACAT[-/AT]ATATATATATATTTT | 6709 |
rs758447673 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579333 | ATAGTAAACAAGTCC[A/G]TTTGGCACAAAGAAG | 6709 |
rs758453647 | snp | A/G | 1.65321e-05 | 0.00287502 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128618070 | GCTGGCGCAGTTTGT[A/G]GAGCACTGGAAAGAG | 6709 |
rs758477426 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591186 | CCTGCATCAGCCTCC[C/T]GAGTAGCTGGGGCTA | 6709 |
rs758484724 | snp | A/G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589100 | GTGACATACATTTAT[A/G/T]CAGTACTGTGTATGA | 6709 |
rs758490204 | snp | A/G | 5.02542e-05 | 0.00501244 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613502 | TAAGCAAAGGGAGGC[A/G]GGCCAGGCCCGAGTG | 6709 |
rs758499840 | snp | C/G | 4.64134e-05 | 0.00481711 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628157 | CCTTCAAGCCAGGGG[C/G]AGCCGTCCTTGCCTC | 6709 |
rs758521158 | snp | C/G | 1.66463e-05 | 0.00288494 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128566968 | TTATAAAGACCCAAC[C/G]AACTTGCAGGTACGT | 6709 |
rs758557229 | in-del | -/CTTC | 4.95487e-05 | 0.00497714 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582467 | ATGAAGAACTCTTAT[-/CTTC]CTTCCTAGGCATTAG | 6709 |
rs758563834 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619308 | AATAAGTACCACAAA[C/T]GGAGTGGCACGAACG | 6709 |
rs758571561 | snp | C/T | | | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128578200 | TGAGCTTGCCAGTGA[C/T]GTGGCTGGGGCTGAA | 6709 |
rs758573213 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590712 | AAAAATTAGCTGTGC[C/G]TGGTGGCGTGCACCT | 6709 |
rs758583178 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558533 | ATTGCATTCCTAGGA[A/G]GTCGTCTCTGTTGTG | 6709 |
rs758588166 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128556773 | TTGTTGTTTTTATTT[A/G]TGGTGTTCAGTCATC | 6709 |
rs758597056 | snp | A/C | 0.000273785 | 0.0116969 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628237 | GAAGGCCAGAGCTGG[A/C]GTCCAGAGGCCCTAA | 6709 |
rs758607934 | snp | A/G | 3.3012e-05 | 0.00406262 | missense | SPTAN1 | GRCh38.p7 | 9:128566799 | TCCAGGAGAGGCGGC[A/G]GCAGGTCCTAGACCG | 6709 |
rs758689464 | snp | A/G | 3.30918e-05 | 0.00406753 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128608879 | TTTCTGACAGGAAGA[A/G]AAGATTGCTGCTCTG | 6709 |
rs758696932 | snp | C/G | 1.75351e-05 | 0.00296095 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609327 | TTGATGTAGCCTTAT[C/G]TTATTGAGTAGATTT | 6709 |
rs758733662 | snp | A/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128591538 | CTGCGTACGTGAAGA[A/G]ATTGGACCCCGCCCA | 6709 |
rs758735687 | snp | A/G/T | 3.3899e-05 | 0.00411686 | downstream-variant-500B, missense | SPTAN1, WDR34 | GRCh38.p7 | 9:128633751 | GGGACCCCTCAGGCC[A/G/T]CCACCTCTGCTGCCA | 6709 |
rs758740577 | snp | A/G | 1.7324e-05 | 0.00294307 | downstream-variant-500B, intron-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128634023 | GTAAGAGAAACTCTA[A/G]AGACCAACCACATGG | 6709 |
rs758760557 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570818 | TGCGCTGTGCCACCA[C/T]AGCCAGCTAATTTTG | 6709 |
rs758800502 | snp | G/T | | | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128551000 | AGTGGGTAGGGAAAT[G/T]TTTCCTCAGTATCAT | 6709 |
rs758806011 | snp | G/T | 1.65195e-05 | 0.00287393 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584549 | GCTTCCCTCAGGTAG[G/T]AATCAACTTGGGAAA | 6709 |
rs758830664 | snp | A/G | 1.64754e-05 | 0.00287009 | missense | SPTAN1 | GRCh38.p7 | 9:128577352 | GGAGTTCATTTCTAG[A/G]TCAAAGCCCTGTGTG | 6709 |
rs758845025 | snp | A/G | 1.64928e-05 | 0.00287161 | missense | SPTAN1 | GRCh38.p7 | 9:128605428 | GCAGATCAGCGCAAG[A/G]CAAAGTTGGGTGACT | 6709 |
rs758865259 | snp | C/T | 6.74752e-05 | 0.00580802 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613347 | TGAGTATACACCACA[C/T]AGTAGCCTTTGCTTT | 6709 |
rs758876893 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595958 | AAGTGATCCTCCTGC[C/T]TCAGCCTCCTGAGTA | 6709 |
rs758898666 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612854 | CGCTTGAACCTGGGA[A/G]GTGGAGGTTGCAGTG | 6709 |
rs758898865 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575160 | CATTGTTAACAAATG[C/T]TGGTTGGTGACTCTG | 6709 |
rs758899410 | snp | A/C | 5.57191e-05 | 0.00527792 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621280 | AGCCCATTGGTAAGA[A/C]CTCCATCGCCCACTG | 6709 |
rs758943661 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581194 | AAGAGGGGGAATTGA[A/G]CAAGCTTCTCTCAGC | 6709 |
rs758950723 | snp | C/T | 2.53778e-05 | 0.00356206 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598364 | GACTTTGGCTTGCTA[C/T]TTTGGGTTTTAGTTA | 6709 |
rs758951665 | snp | A/G | 1.6483e-05 | 0.00287076 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582676 | ACTAGAGACTCACAG[A/G]GGATCCTTGTCTTTC | 6709 |
rs758975554 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627355 | TCACTGCCACAGCAG[C/T]GCACAGCATCTGCCC | 6709 |
rs758994692 | snp | G/T | 0.00086145 | 0.020736 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627151 | CAGCAACTCCCTGCT[G/T]GACTGACCAGTCGCT | 6709 |
rs759040222 | snp | G/T | 1.66576e-05 | 0.00288592 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605502 | CATGTTCACTCAGAC[G/T]TCTGGAACATAGAGC | 6709 |
rs759046858 | snp | A/G | 3.3534e-05 | 0.00409461 | downstream-variant-500B, synonymous-codon | SPTAN1, WDR34 | GRCh38.p7 | 9:128633852 | TGTGCCCTGGGCATC[A/G]CCCGCAGCCAAGAGC | 6709 |
rs759054756 | snp | A/T | 2.4406e-05 | 0.0034932 | missense, intron-variant | SPTAN1 | GRCh38.p7 | 9:128593014 | GAGGCCGGCAGTGTA[A/T]CTCTGCGTATGAAGC | 6709 |
rs759057926 | snp | A/G | 1.67396e-05 | 0.00289301 | missense | SPTAN1 | GRCh38.p7 | 9:128576830 | TTGTTTAGGAGCAGC[A/G]CCCTGAGGAGGAACT | 6709 |
rs759068430 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627950 | CTCGATGGGTTAATA[C/T]TGTTTTCTTCCTTCT | 6709 |
rs759088264 | snp | A/G | 1.65241e-05 | 0.00287433 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128618061 | CCAGCAGCGGCTGGC[A/G]CAGTTTGTGGAGCAC | 6709 |
rs759091303 | snp | A/G | 1.65015e-05 | 0.00287237 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612058 | TGAGCTTTAGGAGAG[A/G]GACGATTCTTCATAG | 6709 |
rs759108378 | snp | A/C/G | 3.29453e-05 | 0.00405854 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581736 | ACAGTCTTAGAAGAT[A/C/G]AAAGGAATAGGACAT | 6709 |
rs759115075 | snp | C/T | 1.64955e-05 | 0.00287184 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605201 | GACCCAAAGTCATCT[C/T]CTGTCTGGCATTTTT | 6709 |
rs759116624 | snp | A/T | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554789 | TGGGGGCCACTTGAC[A/T]GGAGCAGCTGTGCTG | 6709 |
rs759120249 | snp | A/G | 1.6501e-05 | 0.00287232 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128626423 | GACCTTCGCCAAAAA[A/G]GCTTCTGCCTTCAAC | 6709 |
rs759162715 | snp | C/T | 1.65015e-05 | 0.00287237 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632555 | CCTGCTGAGCCGCCC[C/T]CGGCTTTGTGCTGCA | 6709 |
rs759166749 | snp | A/T | 1.64727e-05 | 0.00286986 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618824 | AACTATCACAATCAA[A/T]GCTGGAGGAGATTAT | 6709 |
rs759186785 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580029 | GAAACAAATTTTTAT[A/G]AAATGATACATAGGC | 6709 |
rs759204260 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625724 | GGAAGAGCAAGTTCC[A/G]GTCCTGTGGAGTCAC | 6709 |
rs759235351 | snp | C/G/T | 5.1274e-05 | 0.00506308 | downstream-variant-500B, missense | SPTAN1, WDR34 | GRCh38.p7 | 9:128633938 | GCTTGATCAAAACTG[C/G/T]GGGTTTCTGGGAGCT | 6709 |
rs759240730 | snp | C/T | 1.69824e-05 | 0.00291392 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632990 | GGTGAAGAGGTGTCC[C/T]TTGGAAAACTAAAGC | 6709 |
rs759241143 | snp | C/T | 0.000131843 | 0.00811815 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128611824 | ACGTGGAGCCTGTGC[C/T]GGCAGTGAGGATGCT | 6709 |
rs759256279 | snp | A/G | 1.64993e-05 | 0.00287218 | missense | SPTAN1 | GRCh38.p7 | 9:128585807 | AACCAAAAGTGGGAG[A/G]CACTGAAAGCCAAAG | 6709 |
rs759274173 | snp | A/T | 1.64768e-05 | 0.00287021 | missense | SPTAN1 | GRCh38.p7 | 9:128583935 | ACCTCCAGAAGAAAC[A/T]TGCACTGCTAGAGGC | 6709 |
rs759328515 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586363 | GTTTCAAACTCCTGG[A/C]CTCAAACAATCCTCC | 6709 |
rs759365509 | snp | A/G | 1.648e-05 | 0.0028705 | missense | SPTAN1 | GRCh38.p7 | 9:128605096 | TAAACACAGACAATT[A/G]TGGACATGATCTCGC | 6709 |
rs759390847 | snp | A/G | 4.29923e-05 | 0.00463619 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628207 | TCACTTTGGGTAGGG[A/G]AGGTGATGAAGCACG | 6709 |
rs759397261 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604794 | AAATTAGCTGGGCAT[G/T]GTGGTGGGCGCCTGT | 6709 |
rs759411880 | snp | A/C | 1.6473e-05 | 0.00286988 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587737 | TTACTGGAGGGAGGC[A/C]TTGAAGGACTCAGAT | 6709 |
rs759416621 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618447 | ATGATGTTCCATGGA[C/T]GGCCTGACTGACTGT | 6709 |
rs759466862 | snp | C/T | 5.12571e-05 | 0.0050622 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577554 | CATTTGGCTTCTTTT[C/T]TGGAAGCAGGAATAG | 6709 |
rs759470235 | snp | C/G | 6.62581e-05 | 0.0057554 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584245 | ACGATAAAACCACAC[C/G]CAAAGTAAAGTCTGC | 6709 |
rs759471270 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559315 | ATTGGCAGGATCAAA[A/T]CAGCAAGCTGGGCCC | 6709 |
rs759490192 | snp | A/G | 1.64836e-05 | 0.0028708 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582654 | GGATATCCCTTTGGG[A/G]GTGAACACTAGAGAC | 6709 |
rs759547368 | snp | C/T | 0.000218555 | 0.0104513 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627053 | CCTGGCCTCAAGCAG[C/T]CCTCCTGCCCAGGCC | 6709 |
rs759573145 | snp | C/T | 3.29587e-05 | 0.00405934 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128568891 | TTTTGCATCTGAAAC[C/T]ATACGGGTGAGTATG | 6709 |
rs759580317 | snp | A/G | 1.6473e-05 | 0.00286988 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584713 | TGGGGACTGGTGTCT[A/G]CTTTCAGGTAAGGAT | 6709 |
rs759585366 | snp | C/T | 1.6676e-05 | 0.00288751 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630211 | TTAGGTTTGGTTTCC[C/T]TAAAAGGAATGTGAG | 6709 |
rs759591341 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603781 | TGGTGGCTTTCCTGG[G/T]CAAGAGCCTGCCAGT | 6709 |
rs759595099 | snp | C/T | | | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128583891 | CTTGGCTTCGGATGA[C/T]TACGGCAAAGATCTT | 6709 |
rs759613428 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585016 | CTGAGCCTGAATTTC[C/T]TTTTTTTTTTTTTTT | 6709 |
rs759619994 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128607700 | ATTGCTGGAGCGACA[C/T]CAGGTGGGTGGACCT | 6709 |
rs759624358 | snp | G/T | 1.6492e-05 | 0.00287154 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584884 | GCTTGGTGCTGCTCC[G/T]CGTGTCTCCCCTTCT | 6709 |
rs759648854 | snp | A/G | 4.95078e-05 | 0.00497508 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632494 | GTTTAAGTGAGTTCA[A/G]CCTTACTCGCCCTGG | 6709 |
rs759651022 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628801 | GGACGTAGGGATCGC[A/C]GTTTCCGGCCTGTGC | 6709 |
rs759686128 | snp | A/G/T | 0.0001628 | 0.00902073 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628213 | TGGGTAGGGAAGGTG[A/G/T]TGAAGCACGAAGGCC | 6709 |
rs759707900 | snp | C/T | 1.66023e-05 | 0.00288113 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605487 | TTTCCGGTACGGAGC[C/T]ATGTTCACTCAGACT | 6709 |
rs759713935 | snp | C/T | | | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128607869 | ACACCGGACAGAAAT[C/T]GATGCCAGGGCTGGC | 6709 |
rs759717081 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597309 | ACACCTGGCCTCATC[A/G]CATTTTTAAAACATT | 6709 |
rs759724971 | snp | A/G | 1.9359e-05 | 0.00311113 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609692 | ATTTTTTTAAGAGTT[A/G]TAGTTAAATGAGCTC | 6709 |
rs759733391 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617394 | CTAGTGATGCCTCCC[A/G]TCCTCCAGTGCATCC | 6709 |
rs759778130 | snp | C/T | | | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128550784 | GATCAAACATTTTAC[C/T]GCAACCTGCTGGAGA | 6709 |
rs759789796 | snp | A/G | 6.59076e-05 | 0.00574016 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598938 | TTCTTCTAATAATAA[A/G]ACTGGTTTCTCTCTC | 6709 |
rs759794341 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623271 | GATGGGGTCTCACTA[C/T]GTTATGTTGCCCAGG | 6709 |
rs759822213 | snp | A/C/T | 8.23749e-05 | 0.00641728 | missense | SPTAN1 | GRCh38.p7 | 9:128582733 | CACGAGAGAGCCATG[A/C/T]GTCGCCGGGCCCAGC | 6709 |
rs759833805 | snp | A/G/T | 0.000329407 | 0.0128297 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128591527 | TTTTGTGCCGGCTGC[A/G/T]TACGTGAAGAAATTG | 6709 |
rs759836116 | snp | C/T | 1.80188e-05 | 0.00300151 | missense | SPTAN1 | GRCh38.p7 | 9:128604380 | GAGGAACGGAGCCAG[C/T]TCTTGGGCAGCGCCC | 6709 |
rs759839253 | in-del | -/T | 4.94205e-05 | 0.0049707 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581751 | CAAAGGAATAGGACA[-/T]TATTCTGAACACTTT | 6709 |
rs759842941 | snp | A/C | 2.84079e-05 | 0.0037687 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128627416 | CTGCAGAAGGAACAG[A/C]GGCGGCAGGAGGAGA | 6709 |
rs759847363 | in-del | -/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566156 | GAACTCCTGGGCTCA[-/G]GGTGATCCTCCTGCC | 6709 |
rs759853722 | snp | C/T | 1.65891e-05 | 0.00287998 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128577462 | CTGGGAGCAGATCCG[C/T]ACCTTGGCGGCAGAG | 6709 |
rs759861156 | in-del | -/TGTGTAACTGGTTGCC | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601303 | ATTTATAACTGTGAT[-/TGTGTAACTGGTTGCC]TGTGTAACTGGTTGC | 6709 |
rs759865868 | snp | A/G | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128553504 | ATACCACTGTTGAAT[A/G]ATAGAACAGTCTTTT | 6709 |
rs759866080 | in-del | -/G | 3.29462e-05 | 0.00405857 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627981 | CTGGGCTTGTCATGT[-/G]GGGGTCTCGTGCGCT | 6709 |
rs759890585 | snp | C/G | 0.00210681 | 0.0323877 | missense | SPTAN1 | GRCh38.p7 | 9:128575293 | AAACAGATATGGCTG[C/G]TCATGAAGAAAGAGT | 6709 |
rs759910131 | snp | A/G | 1.64969e-05 | 0.00287196 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128580924 | CTATGCCCCCAAGCT[A/G]ACCGTCCTTTCCGAG | 6709 |
rs759921453 | snp | C/T | 1.67024e-05 | 0.0028898 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632344 | CGGGAGGGCTGTGGG[C/T]CAGGCTCAGCCCAGA | 6709 |
rs759953755 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593707 | GAGATAAAACATCCT[A/G]TATGAGGATATTTTA | 6709 |
rs759959490 | snp | C/G | 1.6525e-05 | 0.00287441 | missense | SPTAN1 | GRCh38.p7 | 9:128625778 | GTTCAGGAAACTTTT[C/G]ACGCTGGGCTGCAGG | 6709 |
rs759969257 | snp | A/G | 4.96989e-05 | 0.00498467 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608326 | TTTTTCCTGATTGAC[A/G]TCTGTTTCTTGGCTT | 6709 |
rs759975874 | snp | C/T | 1.65288e-05 | 0.00287474 | missense, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633314 | TACGTGGAGTTCACC[C/T]GCTCGCTTTTCGTGA | 6709 |
rs760027935 | in-del | -/AG | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560570 | ATTTTTAGTAGAGAC[-/AG]AATTTTATCACGTTG | 6709 |
rs760039527 | snp | C/T | 1.75687e-05 | 0.00296379 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583292 | GAAAGGTAAGAGATG[C/T]TCCATTGAATTGTGA | 6709 |
rs760049403 | in-del | -/AC | 0.000132897 | 0.00815051 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632376 | CAGGGGGAGGAAAAG[-/AC]ACAGTCACCTGCTGT | 6709 |
rs760049572 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565183 | TGGTGCAGGCCTGTA[G/T]TCCCCGCTACTCGGG | 6709 |
rs760062256 | snp | A/C | 1.6638e-05 | 0.00288422 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584021 | TGCAGAAACTATAGG[A/C]GGGAGGAAAAGCCAG | 6709 |
rs760071427 | snp | C/G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558827 | GTAACTGACAGTTTC[C/G/T]GGTGAGAGGCTGTAG | 6709 |
rs760127971 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611599 | GTTAAAAACGTTGGC[A/G]TTTACCCCAGTTCTT | 6709 |
rs760137388 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621438 | CCCCTTTTTGAAGCC[A/G]GTAAAGTTATTCTGC | 6709 |
rs760156963 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578690 | AACAGTTAGCTGGTC[A/G]TGGTGGCACGCGCCT | 6709 |
rs760175003 | snp | G/T | 1.65091e-05 | 0.00287303 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632511 | CTTACTCGCCCTGGC[G/T]GGGTGGGGGGTGTTC | 6709 |
rs760181440 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579850 | TCACCATGATATGTG[A/G]GAAACTTTCCTTTCT | 6709 |
rs760192480 | snp | A/G | 1.64866e-05 | 0.00287106 | missense | SPTAN1 | GRCh38.p7 | 9:128581024 | CTCTTCTACCGGGAC[A/G]CTGAGCAGGTGGACA | 6709 |
rs760242561 | snp | A/G | 1.65187e-05 | 0.00287386 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592933 | CCTTTCATCCCTGTG[A/G]ATTAACCCCACTAAT | 6709 |
rs760243298 | snp | C/T | 1.64811e-05 | 0.00287059 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128625894 | GGCCCGGCACGCCTC[C/T]CTCATGAAGAGGTGG | 6709 |
rs760255841 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570012 | ATTTAACCCATTTGG[C/G]CAATGTAATATGTGT | 6709 |
rs760281970 | snp | C/T | 6.59141e-05 | 0.00574045 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128583894 | GGCTTCGGATGATTA[C/T]GGCAAAGATCTTACC | 6709 |
rs760282548 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596301 | TTGTTTTTCGAGACA[A/G]AGTCTCTCTCTGTTG | 6709 |
rs760298084 | snp | A/G | 0.000132089 | 0.00812572 | missense | SPTAN1 | GRCh38.p7 | 9:128618054 | AGGAGATCCAGCAGC[A/G]GCTGGCGCAGTTTGT | 6709 |
rs760310956 | snp | A/G | 1.67295e-05 | 0.00289214 | downstream-variant-500B, missense | SPTAN1, WDR34 | GRCh38.p7 | 9:128633835 | AGCTGCCACACCTTC[A/G]CTGTGCCCTGGGCAT | 6709 |
rs760332947 | snp | C/T | | | downstream-variant-500B, synonymous-codon | SPTAN1, WDR34 | GRCh38.p7 | 9:128633855 | GCCCTGGGCATCGCC[C/T]GCAGCCAAGAGCTGA | 6709 |
rs760385888 | snp | C/T | 1.6486e-05 | 0.00287102 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617973 | CTGTTAACCTCCTCG[C/T]CCTTGCCTGTCAGGG | 6709 |
rs760386687 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623020 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCGTGAG | 6709 |
rs760387334 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602534 | TTGTTCTTTACTCAA[A/G]GGGTTGTGAGCATTA | 6709 |
rs760401725 | snp | A/T | 5.16151e-05 | 0.00507985 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588981 | GTGTTTGTTCCACGC[A/T]GGCACCTCCACGTAT | 6709 |
rs760402274 | snp | C/T | 1.67928e-05 | 0.0028976 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598553 | GCTGTAAGGATGCAG[C/T]TTTGTTCCTCTTGTG | 6709 |
rs760403309 | snp | C/G | 1.64917e-05 | 0.00287151 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605181 | TCTCGGTGACAAGGT[C/G]AGAGGACCCAAAGTC | 6709 |
rs760414043 | snp | A/G | 3.29451e-05 | 0.00405851 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128607664 | AGATGAGCTAGCCAA[A/G]GATGTCACCGGAGCT | 6709 |
rs760414636 | snp | A/G | 1.65288e-05 | 0.00287474 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587590 | CACAGTGCTCCATGT[A/G]TGGTTTTGGTTTCAG | 6709 |
rs760419507 | snp | A/G | 4.96471e-05 | 0.00498208 | missense | SPTAN1 | GRCh38.p7 | 9:128575335 | ACCAGTTTGCTGCCA[A/G]ACTCATACAGGTAAA | 6709 |
rs760476702 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617199 | AGCAGAGATCATGCC[A/G]TTGCACTTTAGCCTG | 6709 |
rs760489531 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608485 | AAAAATATTATCAAA[A/G]GGATGGAAAACAAAT | 6709 |
rs760494676 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610525 | GAAATGAAACATTTG[A/C]TGCAGAATTCCCCAA | 6709 |
rs760519581 | snp | A/T | 3.30617e-05 | 0.00406568 | missense | SPTAN1 | GRCh38.p7 | 9:128577445 | GAGGAACTGATTACA[A/T]ACTGGGAGCAGATCC | 6709 |
rs760535542 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603721 | TCTATTGGGTCCAAG[C/T]ATGTCCTAAGTAAAC | 6709 |
rs760552878 | snp | A/G | 3.30338e-05 | 0.00406397 | missense | SPTAN1 | GRCh38.p7 | 9:128566874 | TGGAAGATTCCTATC[A/G]ATTCCAGTTCTTTCA | 6709 |
rs760571561 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572357 | CTCCCTGCCCACTCA[C/T]GCTCTCAAATAATAG | 6709 |
rs760576677 | snp | A/G | 1.64732e-05 | 0.0028699 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577293 | GTTTTACAAGCAGCT[A/G]ATTCTGTAAATAAGT | 6709 |
rs760597106 | snp | C/T | 1.65455e-05 | 0.00287619 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568730 | ACAAAATGCTGATGC[C/T]GTGTGGTTGCGTCTG | 6709 |
rs760600514 | snp | A/G | 1.69367e-05 | 0.00290999 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587721 | TGTAACAGTTTATGG[A/G]TTACTGGAGGGAGGC | 6709 |
rs760603381 | in-del | -/TGTT | 1.70041e-05 | 0.00291577 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588967 | CAGAGAGTGGCTGTG[-/TGTT]TGTTCCACGCTGGCA | 6709 |
rs760607569 | snp | C/T | 1.64779e-05 | 0.00287031 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582597 | CTCCTTTTTGGTACA[C/T]GAATGTCTCTTCTAA | 6709 |
rs760617530 | snp | C/T | 1.89166e-05 | 0.00307538 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628185 | CTCACTGGGCGATTC[C/T]AAGGGCTCACTTTGG | 6709 |
rs760620533 | snp | C/T | 1.65239e-05 | 0.00287431 | missense | SPTAN1 | GRCh38.p7 | 9:128584505 | GAGAGAAAGAGCCCA[C/T]TGCCGCATCTACCAA | 6709 |
rs760625641 | snp | A/G | 1.70653e-05 | 0.00292102 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613534 | CTGGGACACAGCTCT[A/G]CCTGACTCCTAAGGA | 6709 |
rs760646885 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602319 | CCTCCTGGGTTCAAG[C/T]AATTCTCCCACCTCA | 6709 |
rs760654962 | snp | C/T | 0.000198768 | 0.00996716 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608853 | GGCCCACCTTGATCT[C/T]ATGCCTTTGTTTTCT | 6709 |
rs760697173 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128609206 | GTTCAGCCGGGATGT[A/G]GATGAGATTGAGGCT | 6709 |
rs760712681 | snp | C/T | 1.69942e-05 | 0.00291493 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577532 | TGCTCCAGGTCTTAA[C/T]CAGTATCATTTGGCT | 6709 |
rs760717733 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620633 | TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG | 6709 |
rs760722637 | snp | C/T | 1.662e-05 | 0.00288266 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624324 | GCCTCTCTCCATGGC[C/T]TAGAACAATCACCAT | 6709 |
rs760723694 | in-del | -/CCTGCTCC | 1.66801e-05 | 0.00288787 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632353 | GTGGGCCAGGCTCAG[-/CCTGCTCC]CCCAGAGCAGGGGGA | 6709 |
rs760737365 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595407 | GAGCTACCATGCCTG[A/G]CCTGTGTAGCTATTT | 6709 |
rs760746122 | in-del | -/CA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595110 | CACCGTGCCCGGCCT[-/CA]CAGTTTTTTTTTTGT | 6709 |
rs760747143 | snp | G/T | 1.68196e-05 | 0.00289992 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609312 | GACTGGGTGTTGGTC[G/T]TGATGTAGCCTTATG | 6709 |
rs760748641 | snp | C/T | 1.66463e-05 | 0.00288494 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632907 | GAGCGCCTTCCGGGC[C/T]CTCAGCTCAGAGGGA | 6709 |
rs760754037 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597085 | AGATCGCTTGAACCC[A/G]GGAGGCGGAGGTTGC | 6709 |
rs760755333 | snp | A/T | 3.29457e-05 | 0.00405854 | missense | SPTAN1 | GRCh38.p7 | 9:128591572 | AGCCTCCCGGGAGAA[A/T]CTCCTGGAGGAGCAA | 6709 |
rs760762327 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564000 | ATACAGGACCGGACA[C/T]GGTGGCTTACACCTG | 6709 |
rs760764559 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629242 | TACTGATGCACTCTT[A/G]ACATCCCCAGGCGGC | 6709 |
rs760791147 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566092 | GTTTTTGTTTTGTTT[C/T]GTCACCCAGGGCGGA | 6709 |
rs760815035 | snp | A/G | 1.64765e-05 | 0.00287019 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128574734 | GAAGATGCGAGAAAA[A/G]GGAATCAAACTGCTG | 6709 |
rs760820851 | snp | C/G | 1.65542e-05 | 0.00287695 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582855 | AGCTTATAAAGTAAT[C/G]TACTGTTAGTGTTGC | 6709 |
rs760837405 | snp | C/T | 0.00285469 | 0.0376722 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626973 | GCACGTGCCACCACG[C/T]CTGGCTAATTATTTT | 6709 |
rs760865353 | snp | A/G | 1.65135e-05 | 0.00287341 | missense | SPTAN1 | GRCh38.p7 | 9:128617720 | GGAAGAAGCACAAGC[A/G]GCTGGAAGCAGAACT | 6709 |
rs760898575 | snp | C/T | 1.66804e-05 | 0.00288789 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621112 | GGGCCTAGCCCACAA[C/T]ACATAGCAGGCTCTC | 6709 |
rs760925342 | snp | A/G | 1.97252e-05 | 0.00314042 | missense | SPTAN1 | GRCh38.p7 | 9:128626653 | CCATGGAGGCCCTGG[A/G]GGAGACCTGGAGGAA | 6709 |
rs760928451 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576716 | TTTCTTGTGATTCTC[C/T]TCAGAGTGGTGATTT | 6709 |
rs760931553 | snp | A/T | | | missense | SPTAN1 | GRCh38.p7 | 9:128607667 | TGAGCTAGCCAAGGA[A/T]GTCACCGGAGCTGAG | 6709 |
rs760955571 | snp | G/T | 3.29457e-05 | 0.00405854 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584702 | GGTTGGATAACTGGG[G/T]ACTGGTGTCTGCTTT | 6709 |
rs760960101 | snp | C/G | 6.58903e-05 | 0.00573941 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128608141 | TTAGCTGTTCCATCG[C/G]GACTGTGAGCAAGCT | 6709 |
rs760963985 | snp | C/T | 0.0012367 | 0.0248359 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628150 | GATAGAGCCTTCAAG[C/T]CAGGGGGAGCCGTCC | 6709 |
rs760984212 | snp | A/G | 1.64825e-05 | 0.00287071 | missense | SPTAN1 | GRCh38.p7 | 9:128582497 | TTAGATGAATTTGCA[A/G]CCAAGCTAATTCAGA | 6709 |
rs761013466 | in-del | -/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574976 | CTCTCTAGGTGTATG[-/C]TGCTATTCTGTAACT | 6709 |
rs761046056 | snp | A/G | 1.64754e-05 | 0.00287009 | missense | SPTAN1 | GRCh38.p7 | 9:128608008 | CTGGAGAAGGCCTGG[A/G]TTCAGCGCAGGATGA | 6709 |
rs761056993 | snp | A/C | 1.65592e-05 | 0.00287738 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128583151 | AGCAAACCAGAGCCG[A/C]ATTGATGCCTTGGAG | 6709 |
rs761062286 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128555950 | TCTCGGGCTGGGTGC[A/G]GTGGCTCATGCCTGT | 6709 |
rs761085721 | snp | C/T | 0.000162272 | 0.00900608 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128555449 | TTTGGTTTTGCCTGG[C/T]TTGCAGTGAAGGCAT | 6709 |
rs761088426 | in-del | -/AG | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618668 | TTTTGTATTTTTAGT[-/AG]AGACGGGGTTTCACC | 6709 |
rs761093460 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620277 | GTTAGCTTTGAGCCA[C/T]CTTCCTCACCATGGG | 6709 |
rs761106919 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587142 | TAGGGCTGGAGTACA[A/G]TGATGCAATCACGAC | 6709 |
rs761107143 | snp | A/G | | | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128574770 | CCAGAAGTTGGTGCA[A/G]TACTTACGAGAATGT | 6709 |
rs761115830 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128552980 | GTCCCTCCCAACCAC[C/T]CCCAAGCCTGGCTGC | 6709 |
rs761152561 | snp | C/G | 1.64732e-05 | 0.0028699 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603632 | ATCTCCCCTGGTTTT[C/G]TCCACTATCTTCCTT | 6709 |
rs761166458 | snp | C/T | 4.95528e-05 | 0.00497734 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128585950 | TGACTATGGCAAGGA[C/T]GAAGACTCTGCTGAG | 6709 |
rs761170802 | in-del | -/C/CCC | 0.000426274 | 0.0145939 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627367 | AGCGCACAGCATCTG[-/C/CCC]CCCCCCTTTGGCCCT | 6709 |
rs761239748 | snp | G/T | 1.6593e-05 | 0.00288031 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625733 | AGTTCCAGTCCTGTG[G/T]AGTCACCACAAATTG | 6709 |
rs761261114 | snp | G/T | 1.65015e-05 | 0.00287237 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128579672 | AGACAGCTTCAAATC[G/T]GCAGATGAATCTGGA | 6709 |
rs761301676 | snp | C/T | 4.40859e-05 | 0.00469478 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628113 | GTGTGCCTTGCCCCA[C/T]AGCCCATGGTCCCTG | 6709 |
rs761303153 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586512 | TCACCTTCAACCGTT[A/G]ACATTTGTCACTCTT | 6709 |
rs761308461 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606224 | AAAATACAAACCAGC[C/T]GGGCGTGGTGGCACA | 6709 |
rs761321966 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589954 | TGTGACCTCACCCCA[C/T]AGGCTTTGTCTTCTT | 6709 |
rs761329975 | snp | A/G | 4.94425e-05 | 0.0049718 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625094 | TATTTTCCACACTTC[A/G]TTTTCTAGGTGAAAA | 6709 |
rs761348166 | snp | C/T | 1.65784e-05 | 0.00287905 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608828 | GCAGTCCAGGCAGGG[C/T]CCAGCCACAGGCCCA | 6709 |
rs761359644 | snp | C/G | 4.22386e-05 | 0.00459538 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604422 | AGGTTCCACAGGTGA[C/G]GGGTCAGCCCTGGGC | 6709 |
rs761383095 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620512 | ACCTGAGGTCAGGAG[G/T]CCGAGACCAACCTGG | 6709 |
rs761409296 | snp | A/G | 3.29598e-05 | 0.00405941 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128625885 | GGCCATCGAGGCCCG[A/G]CACGCCTCCCTCATG | 6709 |
rs761414918 | snp | A/G | | | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128552196 | GCGGAGTGGTGCGAT[A/G]CAGACGACTGTCCGC | 6709 |
rs761438413 | snp | C/G | 1.6477e-05 | 0.00287024 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128613413 | ATCCGAAGATTATGG[C/G]AAAGACCTAGCTTCT | 6709 |
rs761455344 | snp | G/T | 3.29881e-05 | 0.00406115 | missense | SPTAN1 | GRCh38.p7 | 9:128577414 | TCTGAGTGCAACACA[G/T]ATTCAAGTGAAGCGA | 6709 |
rs761469673 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557500 | CCACCCACTGCCTCT[A/G]CCTGTACAAGAAGAT | 6709 |
rs761476736 | in-del | -/T | 1.69375e-05 | 0.00291006 | downstream-variant-500B, frameshift-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128633908 | GACAGTAGACAGGGC[-/T]TTCATCCTGGGTTTG | 6709 |
rs761480637 | snp | A/G | 3.44145e-05 | 0.00414802 | downstream-variant-500B, intron-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128633988 | TGCACGTCACCTGCA[A/G]AGAGAGACAGATACG | 6709 |
rs761482297 | snp | C/T | 3.2987e-05 | 0.00406108 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582476 | TCTTATCTTCCTTCC[C/T]AGGCATTAGATGAAT | 6709 |
rs761490801 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582632 | TTCCAGTTAAGTCTC[C/T]TCAACTGGATATCCC | 6709 |
rs761497374 | snp | C/T | 3.54522e-05 | 0.00421009 | downstream-variant-500B, utr-variant-3-prime | SPTAN1, WDR34 | GRCh38.p7 | 9:128633705 | TCAGAAACACAAGGC[C/T]CGGCACAGCGAAGGC | 6709 |
rs761497643 | snp | A/G | 1.65002e-05 | 0.00287225 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128625789 | TTTTGACGCTGGGCT[A/G]CAGGCCTTCCAGCAG | 6709 |
rs761497732 | snp | A/G | 7.93116e-05 | 0.00629678 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628180 | CTTGCCTCACTGGGC[A/G]ATTCCAAGGGCTCAC | 6709 |
rs761499644 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571544 | GAGCCGAGATCCTGC[C/T]ATTGCACTCTGGCTT | 6709 |
rs761533526 | snp | C/T | 3.31011e-05 | 0.0040681 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609291 | AACATCCAGGTAAGC[C/T]GAAGTGACTGGGTGT | 6709 |
rs761538979 | snp | C/T | 1.64787e-05 | 0.00287038 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128594178 | GAATTCCATCAGATA[C/T]CATTCTCTGCTGGAA | 6709 |
rs761540895 | snp | A/G | 1.65433e-05 | 0.002876 | missense | SPTAN1 | GRCh38.p7 | 9:128605471 | AGCGCTTCCTTAGCG[A/G]TTTCCGGTACGGAGC | 6709 |
rs761615254 | in-del | -/T | 3.33394e-05 | 0.00408272 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579621 | CAAATCATGGCTTTG[-/T]TTTTTTCTCCTGTAG | 6709 |
rs761619635 | snp | C/T | | | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632898 | GGAGATTGAGAGCGC[C/T]TTCCGGGCCCTCAGC | 6709 |
rs761620444 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601443 | ATAAAAGTAGATCTT[C/T]TGGCTAGGTGTTGTG | 6709 |
rs761628910 | snp | A/G | 1.64969e-05 | 0.00287196 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128605346 | CCAGTCCCATCCCGA[A/G]TCAGCAGAAGACCTG | 6709 |
rs761669609 | snp | C/T | 1.65932e-05 | 0.00288034 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566701 | CATCTATTTTGGTGC[C/T]TATTGGTACTTATCT | 6709 |
rs761676912 | snp | A/T | 1.64727e-05 | 0.00286986 | missense | SPTAN1 | GRCh38.p7 | 9:128577252 | GGGTCTGGAGAGAGA[A/T]CTTGCTGCTCTAGAA | 6709 |
rs761725793 | snp | C/T | 1.65351e-05 | 0.00287528 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619049 | TTCTCTCTTGGCAAC[C/T]GCCTGCTGGTCATCA | 6709 |
rs761739036 | snp | A/G | 3.32237e-05 | 0.00407563 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128594370 | GTTTGATGACTTCCA[A/G]AAGGTATGGGCAGTC | 6709 |
rs761739761 | snp | C/T | 3.30579e-05 | 0.00406544 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632776 | CACCCACCTGCCCTC[C/T]CTGCTCAGGCTCTTG | 6709 |
rs761758977 | snp | A/G | 1.65269e-05 | 0.00287457 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128584494 | GACGTGGATTCGAGA[A/G]AAAGAGCCCATTGCC | 6709 |
rs761778002 | snp | G/T | 4.9552e-05 | 0.0049773 | missense | SPTAN1 | GRCh38.p7 | 9:128566864 | CGTCAGAAGCTGGAA[G/T]ATTCCTATCGATTCC | 6709 |
rs761784727 | snp | A/G | 3.32187e-05 | 0.00407532 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128621208 | CTTCACCGTCCACAA[A/G]GATCGCGTGAATGAT | 6709 |
rs761805865 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581753 | AAGGAATAGGACATT[A/C]TTCTGAACACTTTGT | 6709 |
rs761819410 | in-del | -/CCTT | 4.97022e-05 | 0.00498484 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588790 | TTTTACCATGTTTGC[-/CCTT]CCTTTGGATTTTTAG | 6709 |
rs761842461 | snp | C/T | 1.64806e-05 | 0.00287054 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600156 | TTTTCAAGAGTTTTG[C/T]GAGATCATGAAATAT | 6709 |
rs761851622 | snp | C/T | 1.65594e-05 | 0.0028774 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579632 | TTTGTTTTTTTCTCC[C/T]GTAGGGTGAAATTGA | 6709 |
rs761874094 | snp | A/G | 1.65329e-05 | 0.0028751 | missense, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633250 | CTGCGTCTCCCACAT[A/G]AAGCCCTACGTGGAC | 6709 |
rs761893162 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574434 | AGTAAATCTACCTGT[G/T]AAAGAACTAGAGTAG | 6709 |
rs761923297 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575421 | CAGGATAAAATTTTG[A/G]TGATTGGTCCCCTAA | 6709 |
rs761936734 | snp | C/T | 1.70761e-05 | 0.00292194 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588971 | GAGTGGCTGTGTGTT[C/T]GTTCCACGCTGGCAC | 6709 |
rs761937499 | snp | G/T | 1.65471e-05 | 0.00287633 | missense | SPTAN1 | GRCh38.p7 | 9:128583120 | AGAAGCATCAGGCTT[G/T]TGAGGCTGAGCTCTC | 6709 |
rs761939413 | snp | C/T | 1.6476e-05 | 0.00287014 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128578197 | AGATGAGCTTGCCAG[C/T]GATGTGGCTGGGGCT | 6709 |
rs761941262 | in-del | -/G | 6.7706e-05 | 0.00581794 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613333 | ATTTTCCAGAATGCT[-/G]AGTATACACCACACA | 6709 |
rs761966553 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593109 | CATTCTCCCTCTGCC[A/G]CTTCTCTTGAAGGCC | 6709 |
rs761978444 | snp | C/T | 3.82629e-05 | 0.00437378 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632119 | ATCTGTGCTCCCCAC[C/T]CCTGCAGCGCAAGCA | 6709 |
rs761985691 | snp | A/G | 1.64817e-05 | 0.00287064 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625076 | CCACTGAGGAGGGCA[A/G]TATATTTTCCACACT | 6709 |
rs762018589 | in-del | -/A | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563426 | CAAAAAACAAAAAAC[-/A]AAAAAAACGCCACTT | 6709 |
rs762062651 | snp | A/C | 1.6473e-05 | 0.00286988 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128609167 | GAAAAGGTCAAAGCT[A/C]GGAGAATCTCAAACC | 6709 |
rs762105382 | snp | A/G | 1.64953e-05 | 0.00287182 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611894 | AAGATGACCACCGTC[A/G]CTGTCAACCTGATAT | 6709 |
rs762152171 | snp | A/G/T | 3.30334e-05 | 0.00406397 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617602 | TGAAAGCAGGGAGGT[A/G/T]CAGAGACTGACTGTG | 6709 |
rs762156669 | in-del | -/AAAAAAAAAAAAA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561662 | GCGAGACTCCGTCTC[-/AAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 6709 |
rs762172535 | snp | A/T | 8.23825e-05 | 0.00641751 | missense | SPTAN1 | GRCh38.p7 | 9:128607906 | CAGGCATTTGAGCAG[A/T]TTGGACAGCAGCTGT | 6709 |
rs762186941 | snp | A/G | 1.65138e-05 | 0.00287343 | missense | SPTAN1 | GRCh38.p7 | 9:128585792 | AAGCTTCACGAGCTG[A/G]ACCAAAAGTGGGAGG | 6709 |
rs762216368 | snp | A/G | 9.885e-05 | 0.0070296 | missense | SPTAN1 | GRCh38.p7 | 9:128607985 | TTCTTGACCAGGAGC[A/G]TGCAGACCTGGAGAA | 6709 |
rs762259676 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599371 | AACTCCCAACCTCAG[A/G]TGATCTGCCCACCTC | 6709 |
rs762274238 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586433 | CCACCCCTTCTGGCC[A/C]ATTTTTCACTTTTTA | 6709 |
rs762335564 | snp | C/T | 3.45979e-05 | 0.00415906 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576793 | GCCAGAAGTTGTGTA[C/T]AAATCCAGTCTCTTC | 6709 |
rs762341171 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569852 | TGTTTGTTGTCTCAC[G/T]TTTGCTTGGCAATAC | 6709 |
rs762357753 | snp | C/T | 1.64751e-05 | 0.00287007 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628004 | CGTGCGCTTGCCCCT[C/T]GTGGCCTGGCTTGTG | 6709 |
rs762358113 | snp | C/T | 1.6664e-05 | 0.00288647 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128624444 | TGAGAACTCGGCCTT[C/T]CTTCAGTTCAACTGG | 6709 |
rs762368762 | snp | C/G/T | 4.96942e-05 | 0.00498448 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599084 | ATCAGAATTGCTGTT[C/G/T]CTGAACCTCAGATGC | 6709 |
rs762425781 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612645 | AACATAGAGGTTTTG[G/T]CCAGGTGCAGTGGCT | 6709 |
rs762426669 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557376 | ATTCCATAGAGAAAC[C/T]GACTGCACTCACTGC | 6709 |
rs762428150 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128577219 | GGCAAGTGTTCAGGC[C/T]CTGCTTCGGAAGCAC | 6709 |
rs762436806 | snp | A/G | 1.64985e-05 | 0.0028721 | missense | SPTAN1 | GRCh38.p7 | 9:128632654 | GGCTATGACCTGCCC[A/G]TGGTGGAGGAAGGGG | 6709 |
rs762445932 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627897 | GACACCACCTTGTCT[C/T]CCGGCTGCTTGGATC | 6709 |
rs762453909 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598164 | TGTTGGTTAGGTTGG[G/T]CTCGAACTCCCGACC | 6709 |
rs762490011 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128608187 | GCCCGGGAGGCCTTC[C/T]TGAATACCGAAGACA | 6709 |
rs762495898 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630098 | GGCTCAGCCCTGGCC[C/T]ACACCAAGGCAGCAG | 6709 |
rs762532087 | snp | A/G | 1.65018e-05 | 0.00287239 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612062 | CTTTAGGAGAGGGAC[A/G]ATTCTTCATAGATTT | 6709 |
rs762562063 | snp | A/G | 3.30049e-05 | 0.00406219 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619021 | GAGACAGAAACCAAA[A/G]GTGTCACCTGCTTTC | 6709 |
rs762562811 | snp | C/G | 8.2445e-05 | 0.00641995 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594160 | CCCTCTTGTCACCCT[C/G]TTGAATTCCATCAGA | 6709 |
rs762571659 | snp | A/G | 1.6473e-05 | 0.00286988 | missense | SPTAN1 | GRCh38.p7 | 9:128612163 | GTGCAAAAGTCAGCG[A/G]AAAAGAGCCAGAAAC | 6709 |
rs762572882 | in-del | -/TGT | | | intron-variant, cds-indel | SPTAN1 | GRCh38.p7 | 9:128555368 | CACATTCCTCCATCA[-/TGT]TGTCATCGTTTCGTA | 6709 |
rs762593308 | in-del | -/AT | 1.65021e-05 | 0.00287241 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578083 | ACCTCCGCTGGAAAC[-/AT]AATGTCTTCCTTTGG | 6709 |
rs762618494 | snp | C/T | 1.65337e-05 | 0.00287517 | missense | SPTAN1 | GRCh38.p7 | 9:128584381 | GAAGCCCTCGTGGCT[C/T]GCTATGAGGCACTCA | 6709 |
rs762641891 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614221 | GCACTTTGGGAGGCC[A/G]AGGCAGGCAGATCAT | 6709 |
rs762644827 | snp | C/T | 3.29495e-05 | 0.00405877 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128630351 | AGAGTCGGGGACCCT[C/T]GAATCCCAGCTTGAA | 6709 |
rs762645157 | snp | A/G | 4.94295e-05 | 0.00497115 | missense | SPTAN1 | GRCh38.p7 | 9:128625847 | AAAGATCAGCTTCTC[A/G]CCGCCAAACACGTTC | 6709 |
rs762698933 | in-del | -/T | 1.65086e-05 | 0.00287298 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632515 | CTCGCCCTGGCTGGG[-/T]GGGGGGTGTTCGGCA | 6709 |
rs762702600 | snp | A/T | 3.31164e-05 | 0.00406904 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587583 | GCCCCTGCACAGTGC[A/T]CCATGTGTGGTTTTG | 6709 |
rs762702979 | snp | A/G | 1.65723e-05 | 0.00287852 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128583169 | TGATGCCTTGGAGAA[A/G]GCTGGCCAAAAGCTG | 6709 |
rs762764873 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613025 | ATTGAGGTGTTCCCA[C/G]CCTTTTGGTGTATAT | 6709 |
rs762784302 | snp | A/G | 2.47307e-05 | 0.00351636 | synonymous-codon, intron-variant | SPTAN1 | GRCh38.p7 | 9:128593037 | TATGAAGCAGGTGGA[A/G]GAACTGTGAGTAGGC | 6709 |
rs762808132 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629560 | AAGGCCACACGCACC[A/G]TGTGATTCGTCCCTG | 6709 |
rs762817564 | snp | A/C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564292 | GGCACCATGATGGGC[A/C/G]CCTGTAATCCCAGCT | 6709 |
rs762817568 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562477 | AAGGGAACTTTTTGA[A/G]CTTTCAAATGGACCC | 6709 |
rs762823170 | snp | C/T | 3.35847e-05 | 0.00409771 | downstream-variant-500B, missense | SPTAN1, WDR34 | GRCh38.p7 | 9:128633868 | CCCGCAGCCAAGAGC[C/T]GAGTCTGCTGGCTGT | 6709 |
rs762830545 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592907 | CATCATGGCACCAGT[C/T]GGAGCTGCTGCCTTT | 6709 |
rs762884049 | snp | A/G | 1.71243e-05 | 0.00292607 | downstream-variant-500B, synonymous-codon | SPTAN1, WDR34 | GRCh38.p7 | 9:128633951 | TGTGGGTTTCTGGGA[A/G]CTTTTCTGGAGATCA | 6709 |
rs762887917 | snp | C/T | 9.88321e-05 | 0.00702896 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128581856 | GAAGCACGAAGACTT[C/T]GAGAAATCCCTTAGT | 6709 |
rs762893360 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572919 | AGTTTTGCCAACAGT[A/G]GTGGAAGTGAATTGT | 6709 |
rs762893514 | snp | G/T | 1.69815e-05 | 0.00291384 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588964 | GCACAGAGAGTGGCT[G/T]TGTGTTTGTTCCACG | 6709 |
rs762909288 | snp | A/G | 1.64773e-05 | 0.00287026 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578065 | GCCATTTTCCACCCT[A/G]GAACCTCCGCTGGAA | 6709 |
rs762933433 | snp | C/G | 1.64991e-05 | 0.00287215 | missense | SPTAN1 | GRCh38.p7 | 9:128605336 | AGCGCCTGATCCAGT[C/G]CCATCCCGAGTCAGC | 6709 |
rs762938535 | snp | C/T | 4.94181e-05 | 0.00497057 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618854 | TGGCTGATTTTCTTC[C/T]TGTCTCCTGTAATTA | 6709 |
rs762948878 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588197 | GAGATGGGGTTTCAC[C/T]ATGTTGGCCGGGCTG | 6709 |
rs762956214 | snp | A/G | 1.65927e-05 | 0.00288029 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128624366 | CTCTTCAAAGATGAA[A/G]GGCCTGAACGGGAAA | 6709 |
rs762972879 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558974 | CAAGAGACAGCTCCC[C/T]GTCAGGTTAAGAGGG | 6709 |
rs762990214 | snp | A/T | 1.65548e-05 | 0.002877 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582857 | CTTATAAAGTAATGT[A/T]CTGTTAGTGTTGCCA | 6709 |
rs763025631 | snp | A/G | 1.64887e-05 | 0.00287125 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128626480 | CTTAACAGACCCCGT[A/G]CGCTGCAACTCCTTG | 6709 |
rs763048781 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585318 | ACAGCCATGAGCCAC[C/T]GCGCCTGGCTCCGAG | 6709 |
rs763048947 | in-del | -/GT | 2.57198e-05 | 0.00358598 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598508 | TGCAACAACAGGTAG[-/GT]GTGTCTCCATCTTGG | 6709 |
rs763070314 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586201 | GTGGCTCACTGCAGC[C/T]TCAAACTCCTGGGCT | 6709 |
rs763070641 | snp | G/T | 1.64963e-05 | 0.00287192 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599063 | TATCAAGCCAAGAAC[G/T]TCTTCATCAGAATTG | 6709 |
rs763106093 | snp | A/G | 1.65367e-05 | 0.00287543 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568745 | TGTGTGGTTGCGTCT[A/G]AGGCTCACTTCAAGG | 6709 |
rs763110402 | snp | A/G | 1.64727e-05 | 0.00286986 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627888 | TGTTGTCCGGACACC[A/G]CCTTGTCTCCCGGCT | 6709 |
rs763114925 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604865 | GAACCCGGTGGGGGC[A/G]GAGGTTGCAGTGAGC | 6709 |
rs763156575 | snp | A/G | 3.2956e-05 | 0.00405918 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128607893 | GGCTGGCACTTTCCA[A/G]GCATTTGAGCAGTTT | 6709 |
rs763166606 | in-del | -/TAT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606486 | ACATATATATATATA[-/TAT]TTTTTTTTTGGGGGG | 6709 |
rs763169784 | snp | A/G | 1.65485e-05 | 0.00287645 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630230 | AAGGAATGTGAGGTT[A/G]CCAGGCATTGCTCTC | 6709 |
rs763177607 | in-del | -/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603039 | TAATTCACTGCTTTA[-/T]TTTTTTCCCTCTGGT | 6709 |
rs763178321 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629591 | CACGTAACCCTAACT[C/T]GTTTGTTGTCTTTGT | 6709 |
rs763201456 | snp | C/T | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554433 | ATGGGGAGAGCTGTT[C/T]TAAGTATGTCTTTTG | 6709 |
rs763209520 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582945 | ACGAAATAAGGGATT[C/T]CAGAAACCCCACTAC | 6709 |
rs763235552 | snp | A/G | 3.29783e-05 | 0.00406055 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128588847 | TGAGACTGGGAAGGA[A/G]CTGGTCTTGGCTCTC | 6709 |
rs763242463 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598024 | CGCAATCTCAGCTCA[C/T]CGCAACCTCTGCCTA | 6709 |
rs763250092 | in-del | -/C | 3.29679e-05 | 0.00405991 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611861 | TATGGCCCACCAGCT[-/C]CCCGGTGCCCAGGGA | 6709 |
rs763256328 | snp | A/T | 1.64751e-05 | 0.00287007 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128578158 | CACCAGCTGGGTGAC[A/T]GAGATGAAAGCCCTC | 6709 |
rs763258194 | snp | A/G | 1.70049e-05 | 0.00291585 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128633004 | CTTTGGAAAACTAAA[A/G]CCAAATTTGTGGCAG | 6709 |
rs763259317 | snp | C/G | 1.64732e-05 | 0.0028699 | missense | SPTAN1 | GRCh38.p7 | 9:128584762 | CTGCTAAAGAAACAT[C/G]AAGCCTTACAAGCAG | 6709 |
rs763263796 | snp | C/T | 3.29522e-05 | 0.00405894 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600138 | CTCCTTTGCAAATTA[C/T]TGTTTTCAAGAGTTT | 6709 |
rs763268864 | snp | A/G | 1.64996e-05 | 0.0028722 | missense | SPTAN1 | GRCh38.p7 | 9:128591622 | AGGAGCAGATTGACA[A/G]TCAGTAAGGATGACA | 6709 |
rs763306155 | snp | C/T | 1.66477e-05 | 0.00288506 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128624435 | GAAGCTGGATGAGAA[C/T]TCGGCCTTCCTTCAG | 6709 |
rs763343284 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565962 | GAGGGAAGGTGGCTA[A/G]TGTGAGGTCACATGT | 6709 |
rs763381873 | snp | G/T | 1.64863e-05 | 0.00287104 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617962 | AGAGCTACCTGCTGT[G/T]AACCTCCTCGTCCTT | 6709 |
rs763383640 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627231 | GAAAGAACTACCAAG[C/T]GCTCTGAGCCGGCCT | 6709 |
rs763385120 | snp | A/T | 1.65154e-05 | 0.00287358 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128575309 | TCATGAAGAAAGAGT[A/T]AATGAAGTGAACCAG | 6709 |
rs763416763 | snp | C/T | 1.65021e-05 | 0.00287241 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605025 | AACCTGAATGTGTCT[C/T]GCCTTTAGAGATGCT | 6709 |
rs763458645 | snp | C/T | 4.94784e-05 | 0.00497361 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584889 | GTGCTGCTCCTCGTG[C/T]CTCCCCTTCTTGCCG | 6709 |
rs763473288 | in-del | -/TGT | 1.68279e-05 | 0.00290064 | downstream-variant-500B, cds-indel | SPTAN1, WDR34 | GRCh38.p7 | 9:128633880 | GCTGAGTCTGCTGGC[-/TGT]TGTTGAACTCCAGAC | 6709 |
rs763477441 | snp | C/G | 1.64866e-05 | 0.00287106 | missense | SPTAN1 | GRCh38.p7 | 9:128581009 | TGCATGGACCTGCAG[C/G]TCTTCTACCGGGACA | 6709 |
rs763496889 | snp | A/T | 1.64762e-05 | 0.00287016 | missense | SPTAN1 | GRCh38.p7 | 9:128608020 | TGGGTTCAGCGCAGG[A/T]TGATGCTGGATCAGT | 6709 |
rs763507558 | snp | C/G | 1.64993e-05 | 0.00287218 | missense | SPTAN1 | GRCh38.p7 | 9:128618038 | AACACCATCGGGAAA[C/G]AGGAGATCCAGCAGC | 6709 |
rs763532438 | snp | C/T | 1.64762e-05 | 0.00287016 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607726 | GACCTGCCTGCTGAG[C/T]AGCAAAGACGTGGCT | 6709 |
rs763542381 | snp | C/T | 1.65982e-05 | 0.00288077 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566698 | TTTCATCTATTTTGG[C/T]GCCTATTGGTACTTA | 6709 |
rs763546613 | snp | A/G/T | 9.89273e-05 | 0.00703242 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628031 | TGTGGAGGATCCCGG[A/G/T]ATGGGCCTTCCTGCC | 6709 |
rs763556214 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615402 | AAGCACCAGCATGTC[C/G]CCTCCTCCATTGCTT | 6709 |
rs763573910 | snp | A/G | 1.96593e-05 | 0.00313517 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609709 | AGTTAAATGAGCTCC[A/G]GTATTTGTGTTACTC | 6709 |
rs763575678 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624233 | GGGGAGCAAGTGGCC[C/T]ATTTTATAGAAGTTT | 6709 |
rs763577865 | snp | A/G | 1.74117e-05 | 0.00295052 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576775 | GGGTAACTAGTTGGA[A/G]GAGCCAGAAGTTGTG | 6709 |
rs763603522 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609756 | ATTATTGTGGTCACA[C/T]GGTTTGCTGGTGTCT | 6709 |
rs763633690 | snp | C/G | 1.65018e-05 | 0.00287239 | missense | SPTAN1 | GRCh38.p7 | 9:128632681 | GGGGAACCTGACCCT[C/G]AGTTCGAGGCAATCC | 6709 |
rs763633945 | snp | C/G | 1.64727e-05 | 0.00286986 | missense | SPTAN1 | GRCh38.p7 | 9:128577220 | GCAAGTGTTCAGGCT[C/G]TGCTTCGGAAGCACG | 6709 |
rs763653587 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557398 | ACTCACTGCAGGTGC[C/G]AGGTTTACAGAGTCC | 6709 |
rs763685096 | snp | G/T | 1.78497e-05 | 0.00298739 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604280 | TCTGACTGGGGGCAT[G/T]ACAGGAGAGGGAGTG | 6709 |
rs763698404 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128556326 | ATTTAGTATCTTGAT[A/G]TCCCAAAATAAAAAA | 6709 |
rs763721835 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614244 | CAGATCATGTGAGCC[C/T]AGGAGTTCAAGACCA | 6709 |
rs763722502 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632016 | AATGTTCTTGTTTTA[C/T]GAGGTCTCAGGCCAG | 6709 |
rs763723561 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600206 | TTCTCTGAATATTCA[C/G]CTTAAGTCTTTAGTC | 6709 |
rs763738330 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601345 | TTGCCTGTGTCTCAG[C/T]TCTAGCATCTTCCCT | 6709 |
rs763741137 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590932 | CACAGCTCTGGAGCA[C/T]CTAAGCAGAGAGAAG | 6709 |
rs763742200 | snp | A/T | 3.80554e-05 | 0.00436191 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628097 | TCACCTGATGAGGAG[A/T]GTGTGCCTTGCCCCA | 6709 |
rs763775093 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603510 | TTGCCAGACACTTGA[C/T]TAGTTTTGCCTTCTG | 6709 |
rs763806998 | snp | C/T | 4.95962e-05 | 0.00497952 | missense | SPTAN1 | GRCh38.p7 | 9:128576886 | AATGCAGCCTGGCAG[C/T]GGCTGAAGGGCCTGG | 6709 |
rs763812488 | snp | C/T | 1.66713e-05 | 0.0028871 | missense | SPTAN1 | GRCh38.p7 | 9:128579719 | CTGGTCACTATGCCT[C/T]AGATGAAGTGAGGGA | 6709 |
rs763815198 | snp | G/T | 1.64727e-05 | 0.00286986 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581747 | AGATCAAAGGAATAG[G/T]ACATTATTCTGAACA | 6709 |
rs763832522 | snp | A/G | 1.64849e-05 | 0.00287092 | missense | SPTAN1 | GRCh38.p7 | 9:128611775 | ACGCTGACCGGATCC[A/G]TGGGGTTATCGACAT | 6709 |
rs763846832 | snp | A/T | 1.6473e-05 | 0.00286988 | missense | SPTAN1 | GRCh38.p7 | 9:128608191 | GGGAGGCCTTCTTGA[A/T]TACCGAAGACAAAGG | 6709 |
rs763871077 | snp | C/T | 1.64996e-05 | 0.0028722 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605218 | TGTCTGGCATTTTTG[C/T]CCCAGAAAGAGCAGA | 6709 |
rs763879792 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128581862 | CGAAGACTTTGAGAA[A/G]TCCCTTAGTGCCCAG | 6709 |
rs763880835 | snp | C/G | 1.65018e-05 | 0.00287239 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612066 | AGGAGAGGGACGATT[C/G]TTCATAGATTTCATC | 6709 |
rs763896071 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567714 | GAGACTTGGTAAATC[A/T]TATCAAAAGCAAAGC | 6709 |
rs763900906 | snp | C/T | 1.64885e-05 | 0.00287123 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594161 | CCTCTTGTCACCCTC[C/T]TGAATTCCATCAGAT | 6709 |
rs763909010 | snp | A/G | 1.65899e-05 | 0.00288005 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128583184 | AGCTGGCCAAAAGCT[A/G]ATTGATGTCAACCAC | 6709 |
rs763910617 | in-del | -/G | 0.000280757 | 0.0118448 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632515 | TCGCCCTGGCTGGGT[-/G]GGGGGGTGTTCGGCA | 6709 |
rs763914085 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613039 | AGCCTTTTGGTGTAT[A/G]TATTTTGCTGTAGTG | 6709 |
rs763923412 | snp | A/C | 5.14372e-05 | 0.00507109 | downstream-variant-500B, missense | SPTAN1, WDR34 | GRCh38.p7 | 9:128633961 | TGGGAGCTTTTCTGG[A/C]GATCAAACAGCTGCA | 6709 |
rs763926939 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581644 | ACTTTAGACTTCCTA[A/G]AAGAGATCTTAGAAG | 6709 |
rs763927126 | snp | A/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128632287 | ACCAGCTGGGCATGC[A/G]CATGCAGCACAACCT | 6709 |
rs763928650 | snp | A/G | 3.29772e-05 | 0.00406048 | missense | SPTAN1 | GRCh38.p7 | 9:128626482 | TAACAGACCCCGTGC[A/G]CTGCAACTCCTTGGA | 6709 |
rs763937763 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624872 | CACGTGTCCTGGGTA[A/G]TAGTAATAGCAACTG | 6709 |
rs763963734 | snp | A/G | 3.31219e-05 | 0.00406938 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128618088 | GCACTGGAAAGAGCT[A/G]AAGCAGCTGGCAGCT | 6709 |
rs763975559 | snp | A/G | 1.65329e-05 | 0.0028751 | missense | SPTAN1 | GRCh38.p7 | 9:128584385 | CCCTCGTGGCTCGCT[A/G]TGAGGCACTCAAGGA | 6709 |
rs764018700 | snp | A/G | 1.6476e-05 | 0.00287014 | missense | SPTAN1 | GRCh38.p7 | 9:128630374 | AGCTTGAAGCTACCA[A/G]AGTAAGTGCCCGTGG | 6709 |
rs764024471 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590117 | GTTAAGGCTGGAGAA[A/G]TGTCCTTGGCCATTT | 6709 |
rs764049905 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629701 | GTCCTAGAGAGGAGG[C/T]TCCCTCCCTGGCTGT | 6709 |
rs764068403 | snp | C/T | 3.30191e-05 | 0.00406306 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619033 | AAAGGTGTCACCTGC[C/T]TTCTCTCTTGGCAAC | 6709 |
rs764069090 | snp | C/G | 1.64985e-05 | 0.0028721 | missense | SPTAN1 | GRCh38.p7 | 9:128605341 | CTGATCCAGTCCCAT[C/G]CCGAGTCAGCAGAAG | 6709 |
rs764099271 | snp | A/G | | | downstream-variant-500B, intron-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128634118 | TGCTGGAGGGAAGCC[A/G]TCCTTACCCCCATGT | 6709 |
rs764106606 | in-del | -/T | 1.64806e-05 | 0.00287054 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582644 | CTCTTCAACTGGATA[-/T]CCCTTTGGGAGTGAA | 6709 |
rs764140002 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593053 | GAACTGTGAGTAGGC[C/T]GAGAGTCTTGCAGAG | 6709 |
rs764156958 | in-del | -/T | 0.375 | 0.216506 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612084 | CATAGATTTCATCTC[-/T]TTTTGGCTCCCTTCT | 6709 |
rs764158233 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618855 | GGCTGATTTTCTTCC[C/T]GTCTCCTGTAATTAG | 6709 |
rs764160643 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592908 | ATCATGGCACCAGTC[A/G]GAGCTGCTGCCTTTC | 6709 |
rs764175244 | snp | A/G | 1.6531e-05 | 0.00287493 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568747 | TGTGGTTGCGTCTGA[A/G]GCTCACTTCAAGGTC | 6709 |
rs764203560 | snp | C/G | 1.64882e-05 | 0.00287121 | missense | SPTAN1 | GRCh38.p7 | 9:128615668 | AGCCAGGCAGACAGC[C/G]TGATGACCAGCAGTG | 6709 |
rs764216482 | snp | C/T | 1.64825e-05 | 0.00287071 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568914 | TGAGTATGAGTAGCT[C/T]GTGGAGTGGATGGCT | 6709 |
rs764235299 | snp | C/T | 4.94271e-05 | 0.00497102 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609072 | TCTCCCCACTTCCTT[C/T]TCCACGGTAAGATAT | 6709 |
rs764235462 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629674 | CCAGAGCCCATCTGC[C/T]CTCAGAACTTGGTCC | 6709 |
rs764236974 | snp | C/T | 3.30699e-05 | 0.00406618 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630232 | GGAATGTGAGGTTGC[C/T]AGGCATTGCTCTCTC | 6709 |
rs764247109 | snp | C/T | 1.64765e-05 | 0.00287019 | missense | SPTAN1 | GRCh38.p7 | 9:128615764 | AGCATGGCGGCCTCC[C/T]GGCGAGCCAAGCTGA | 6709 |
rs764260912 | in-del | -/AT | 5.53695e-05 | 0.00526134 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598517 | CAGGTAGGTGTCTCC[-/AT]CTTGGAGTGAGGCTC | 6709 |
rs764263105 | snp | G/T | 1.64762e-05 | 0.00287016 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578071 | TTCCACCCTGGAACC[G/T]CCGCTGGAAACATAA | 6709 |
rs764276461 | snp | A/T | 1.65397e-05 | 0.00287569 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599077 | CTTCTTCATCAGAAT[A/T]GCTGTTCCTGAACCT | 6709 |
rs764281706 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618804 | ACTGTTTTTAAGCAT[A/T]TGTTAACTATCACAA | 6709 |
rs764295713 | snp | G/T | 1.6588e-05 | 0.00287988 | missense | SPTAN1 | GRCh38.p7 | 9:128624368 | CTTCAAAGATGAAGG[G/T]CCTGAACGGGAAAGT | 6709 |
rs764312862 | snp | A/G | 4.96413e-05 | 0.00498179 | missense, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633239 | CAAGCCGACTACTGC[A/G]TCTCCCACATGAAGC | 6709 |
rs764323424 | snp | A/G | 4.94858e-05 | 0.00497398 | missense | SPTAN1 | GRCh38.p7 | 9:128608946 | TATGCCAAGGGAGAC[A/G]TTTCTAGCCGGCGCA | 6709 |
rs764350590 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585329 | CCACCGCGCCTGGCT[C/T]CGAGCCTGAATTTCT | 6709 |
rs764363326 | snp | C/T | 1.72573e-05 | 0.00293741 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611672 | TGAAAAGACATAACC[C/T]AGCAGGAACTGGTTT | 6709 |
rs764384012 | snp | C/G/T | 3.33351e-05 | 0.00408248 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591676 | TCCCATAGGCATACT[C/G/T]TGTTCCACATGGGCC | 6709 |
rs764384954 | snp | C/T | 1.70072e-05 | 0.00291605 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588967 | CAGAGAGTGGCTGTG[C/T]GTTTGTTCCACGCTG | 6709 |
rs764402438 | snp | A/C | 1.70211e-05 | 0.00291724 | downstream-variant-500B, stop-lost | SPTAN1, WDR34 | GRCh38.p7 | 9:128633745 | CCTCCCGGGACCCCT[A/C]AGGCCGCCACCTCTG | 6709 |
rs764415592 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583000 | CATTCCTCCATAAAG[A/G]TAAGTATGAAGGTAG | 6709 |
rs764436806 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573393 | TTTTCACAGAAGGTC[C/T]AAAGTTTTTTCTATC | 6709 |
rs764460035 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128584764 | GCTAAAGAAACATCA[A/G]GCCTTACAAGCAGAA | 6709 |
rs764487156 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623645 | TTTTTTTTTTTTTTT[G/T]TATTTTTTAGAAGAG | 6709 |
rs764505727 | snp | C/T | 0.000359131 | 0.0133954 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627163 | GCTTGACTGACCAGT[C/T]GCTTCCCTCCAGGTC | 6709 |
rs764534295 | in-del | -/AGAC | 1.68972e-05 | 0.0029066 | downstream-variant-500B, frameshift-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128633898 | TGAACTCCAGACAGT[-/AGAC]AGACAGGGCTTTCAT | 6709 |
rs764645623 | snp | A/G | 1.64849e-05 | 0.00287092 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611850 | ATGCTGTCAAGGTAT[A/G]GCCCACCAGCTCCCG | 6709 |
rs764648739 | snp | C/T | 1.64757e-05 | 0.00287012 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598952 | AAACTGGTTTCTCTC[C/T]CTCCTTGTAGGAAGT | 6709 |
rs764666733 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611037 | TACAGCCTGTCTCCA[A/G]TAAGGAGAAAGCCAT | 6709 |
rs764685545 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609869 | TAGCCTGCAACGCCT[C/T]ACTCCCCCTTCTCTC | 6709 |
rs764688062 | snp | A/G | 1.66407e-05 | 0.00288446 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128576843 | GCACCCTGAGGAGGA[A/G]CTGATCAAGACTAAG | 6709 |
rs764704129 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597496 | AATACTCCACTCCAG[C/T]GTGGGTGACAGTGAG | 6709 |
rs764709605 | snp | A/G | | | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128551087 | AGCCAAACTGCAGAG[A/G]GCCAGGAAGCTCAGG | 6709 |
rs764709722 | snp | A/G | 1.64849e-05 | 0.00287092 | missense | SPTAN1 | GRCh38.p7 | 9:128611777 | GCTGACCGGATCCGT[A/G]GGGTTATCGACATGG | 6709 |
rs764734051 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568351 | AAGTGAAAGAAAGTC[C/T]CATGTGTGAGTGAAT | 6709 |
rs764744093 | snp | C/T | 1.64844e-05 | 0.00287087 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576965 | TTAACAGGTGTCAAG[C/T]CAGAGTGGGCTTTGG | 6709 |
rs764760515 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599820 | TTGGTGGTTTTCTTA[C/T]TAAATTTCTTTATTC | 6709 |
rs764791404 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608491 | ATTATCAAAGGGATG[A/G]AAAACAAATGTGTGG | 6709 |
rs764844675 | snp | A/G | 1.64743e-05 | 0.00287 | missense, intron-variant | SPTAN1 | GRCh38.p7 | 9:128593023 | AGTGTATCTCTGCGT[A/G]TGAAGCAGGTGGAAG | 6709 |
rs764853521 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567640 | TGCTGGCAAAAATTT[A/G]TAGTTATTCTGGAGT | 6709 |
rs764875307 | snp | A/G | 1.64974e-05 | 0.00287201 | missense | SPTAN1 | GRCh38.p7 | 9:128632643 | TGCGCTCCCTGGGCT[A/G]TGACCTGCCCATGGT | 6709 |
rs764909398 | snp | C/T | 3.31428e-05 | 0.00407066 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582873 | CTGTTAGTGTTGCCA[C/T]GTAGCACTCGATTAG | 6709 |
rs764933292 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564054 | GGAGGTGGGAGGATC[A/G]TTTGAGCCCAGGAGT | 6709 |
rs764968693 | snp | C/G/T | 4.95081e-05 | 0.00497514 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612061 | GCTTTAGGAGAGGGA[C/G/T]GATTCTTCATAGATT | 6709 |
rs765023796 | snp | G/T | 1.65258e-05 | 0.00287448 | missense | SPTAN1 | GRCh38.p7 | 9:128618065 | CAGCGGCTGGCGCAG[G/T]TTGTGGAGCACTGGA | 6709 |
rs765034111 | snp | C/G | 1.64969e-05 | 0.00287196 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605204 | CCAAAGTCATCTTCT[C/G]TCTGGCATTTTTGCC | 6709 |
rs765036919 | snp | A/G | 1.64955e-05 | 0.00287184 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128585812 | AAAGTGGGAGGCACT[A/G]AAAGCCAAAGCTTCC | 6709 |
rs765075763 | snp | A/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128591565 | CCCAGTCAGCCTCCC[A/G]GGAGAATCTCCTGGA | 6709 |
rs765079561 | snp | C/G | 3.29995e-05 | 0.00406185 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128608936 | TGCCGGCCATTATGC[C/G]AAGGGAGACATTTCT | 6709 |
rs765102345 | snp | G/T | 1.66288e-05 | 0.00288343 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630217 | TTGGTTTCCTTAAAA[G/T]GAATGTGAGGTTGCC | 6709 |
rs765146912 | snp | A/C | 1.69856e-05 | 0.00291419 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632995 | AGAGGTGTCCTTTGG[A/C]AAACTAAAGCCAAAT | 6709 |
rs765186868 | in-del | -/TC | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615182 | ATTCTGGACCGAGTA[-/TC]TCTGTGAGATACCAA | 6709 |
rs765221735 | snp | A/C | 3.31131e-05 | 0.00406884 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584252 | AACCACACCCAAAGT[A/C]AAGTCTGCTCTGTCC | 6709 |
rs765239795 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571860 | TTTGTTTTATTTTAA[G/T]TTATTATTATTTTTG | 6709 |
rs765268035 | in-del | -/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561141 | TTGGGAGGCCGAGGC[-/G]GGCGGACCACAAGGT | 6709 |
rs765268242 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604803 | GGGCATGGTGGTGGG[C/T]GCCTGTAATCCTAGC | 6709 |
rs765270030 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590641 | TGGATCATGTGGTCA[A/G]GAGATTGAGACCATC | 6709 |
rs765271749 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560235 | ATTACAGGCGCACGC[C/T]GCCACACCTGGCTAA | 6709 |
rs765272010 | in-del | -/C | 1.65943e-05 | 0.00288043 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625727 | AGAGCAAGTTCCAGT[-/C]CTGTGGAGTCACCAC | 6709 |
rs765334240 | snp | A/T | 1.65916e-05 | 0.00288019 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588758 | CTCTGTACTTAGATG[A/T]CTCAGCGCGGACGTG | 6709 |
rs765337732 | snp | C/T | 1.66065e-05 | 0.00288149 | missense | SPTAN1 | GRCh38.p7 | 9:128577470 | AGATCCGCACCTTGG[C/T]GGCAGAGAGACATGC | 6709 |
rs765351281 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128556519 | TCATCTGAATTTTGC[A/G]GGTTAAAAGGTAAGT | 6709 |
rs765351333 | snp | G/T | 5.15039e-05 | 0.00507438 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598358 | TCCTTTGACTTTGGC[G/T]TGCTATTTTGGGTTT | 6709 |
rs765359174 | snp | C/T | 1.70889e-05 | 0.00292304 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577555 | ATTTGGCTTCTTTTT[C/T]GGAAGCAGGAATAGC | 6709 |
rs765385842 | snp | A/G | 1.64833e-05 | 0.00287078 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582657 | TATCCCTTTGGGAGT[A/G]AACACTAGAGACTCA | 6709 |
rs765389348 | snp | C/G | 1.66029e-05 | 0.00288117 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615598 | ATAGCTGTGGGAGAC[C/G]CAGTTTCTGACCCTC | 6709 |
rs765393647 | snp | A/G | 6.70747e-05 | 0.00579076 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632943 | TTACGTGACCAAGGA[A/G]GAGCTCTACCAGGTA | 6709 |
rs765401061 | snp | A/G | 1.64754e-05 | 0.00287009 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607712 | ACACCAGGTGGGTGG[A/G]CCTGCCTGCTGAGTA | 6709 |
rs765419678 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582932 | TTGTAGCTAAAGGAC[A/G]AAATAAGGGATTCCA | 6709 |
rs765426245 | snp | A/G | 0.00142784 | 0.0266811 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627091 | GTGCTGGGATTACAG[A/G]TGTGAGCCACTGTAC | 6709 |
rs765426333 | in-del | -/CTT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594804 | CCATCATGTATGTAG[-/CTT]TTTTTTTTTTTTTTT | 6709 |
rs765474158 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597397 | GGCATAGTGGTGTGT[G/T]CCTATAGTCCAAGCT | 6709 |
rs765475658 | snp | G/T | 1.65902e-05 | 0.00288008 | missense | SPTAN1 | GRCh38.p7 | 9:128624360 | GAACATCTCTTCAAA[G/T]ATGAAGGGCCTGAAC | 6709 |
rs765477570 | snp | A/C/T | 3.34965e-05 | 0.00409235 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613501 | GTAAGCAAAGGGAGG[A/C/T]GGGCCAGGCCCGAGT | 6709 |
rs765478546 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595654 | CACCTCTAGTTCCGA[A/G]ACATTTGTGTCACTT | 6709 |
rs765490751 | in-del | -/CTCTCCAGCTCTCC | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574972 | GCTGCTCTCTAGGTG[-/CTCTCCAGCTCTCC]TATGTGCTATTCTGT | 6709 |
rs765496388 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628247 | GCTGGAGTCCAGAGG[C/T]CCTAAGAACCCCCGT | 6709 |
rs765514904 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615902 | GGGCAGCAGGAACCA[C/T]AGGCTGACTGTTGAG | 6709 |
rs765540595 | snp | A/T | 1.65743e-05 | 0.00287869 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128566941 | AAAACTTCAGATTGC[A/T]TCTGATGAGAATTAT | 6709 |
rs765543947 | in-del | -/TC | 1.65102e-05 | 0.00287312 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632415 | GTCTGTTCCCTAATT[-/TC]TGTTTTTCTTCCAGG | 6709 |
rs765556356 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593836 | TTCATCTCGTCTCTC[A/C]ACTGTAGTTGCATGA | 6709 |
rs765589582 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606560 | GCGATCTCAGCTCAC[C/T]GCAACCTCCGCCTCC | 6709 |
rs765591653 | snp | A/T | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128553506 | ACCACTGTTGAATGA[A/T]AGAACAGTCTTTTGT | 6709 |
rs765594683 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609528 | TAGAATCCCCCTTCT[A/G]TTACTGTTCCCAAAT | 6709 |
rs765606539 | in-del | -/CTCGTGCGCTTGCCC | 4.94181e-05 | 0.00497057 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627986 | TTGTCATGTGGGGGT[-/CTCGTGCGCTTGCCC]CTCGTGCGCTTGCCC | 6709 |
rs765619208 | in-del | -/CTT | 1.65051e-05 | 0.00287267 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581902 | ATTACAGTAAGACCC[-/CTT]CTTGTCAGTGCTTTC | 6709 |
rs765625528 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596716 | TATTTTTTAGAGATA[A/G]GGTCTCACTCTCTCA | 6709 |
rs765627152 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565200 | CCCCGCTACTCGGGA[A/G]GCTGAGGCAGGAGAA | 6709 |
rs765662528 | snp | A/G | 1.64751e-05 | 0.00287007 | missense | SPTAN1 | GRCh38.p7 | 9:128574784 | AGTACTTACGAGAAT[A/G]TGAGGACGTGATGGA | 6709 |
rs765667007 | snp | C/G | 2.8245e-05 | 0.00375789 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626694 | ATCATCAAGGTACAC[C/G]TCCCGCTGCCCTCAG | 6709 |
rs765673050 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558835 | CAGTTTCGGGTGAGA[A/G]GCTGTAGCACCTTTG | 6709 |
rs765681529 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621444 | TTTGAAGCCAGTAAA[A/G]TTATTCTGCAGTGCT | 6709 |
rs765693336 | snp | A/G | 1.65067e-05 | 0.00287282 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617634 | TGTTTCCCATCTCTC[A/G]TTCAGGGAGAAGAAG | 6709 |
rs765706270 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128584747 | ATTGGGGTCCAGAAT[C/T]TGCTAAAGAAACATC | 6709 |
rs765715399 | snp | C/T | | | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128550834 | AGCTGTTCTCAGAAA[C/T]GCACACTCCAGGGAG | 6709 |
rs765718120 | snp | C/T | 8.26139e-05 | 0.00642652 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584535 | ACAGAGGTCAGTCTG[C/T]TTCCCTCAGGTAGGA | 6709 |
rs765721940 | in-del | -/TAAA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604938 | CTCCATCTCAGTAAA[-/TAAA]TAAATAAATAAATAA | 6709 |
rs765740646 | snp | A/T | 1.65638e-05 | 0.00287778 | missense | SPTAN1 | GRCh38.p7 | 9:128575344 | CTGCCAAACTCATAC[A/T]GGTAAATAGCAAAGT | 6709 |
rs765774330 | snp | A/G | 0.000123969 | 0.00787206 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609695 | TTTTTAAGAGTTGTA[A/G]TTAAATGAGCTCCAG | 6709 |
rs765778684 | snp | A/G | 1.66029e-05 | 0.00288117 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605488 | TTCCGGTACGGAGCC[A/G]TGTTCACTCAGACTT | 6709 |
rs765787174 | snp | A/G | 3.33656e-05 | 0.00408432 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632346 | GGAGGGCTGTGGGCC[A/G]GGCTCAGCCCAGAGC | 6709 |
rs765788448 | snp | C/T | 1.64901e-05 | 0.00287137 | missense | SPTAN1 | GRCh38.p7 | 9:128591616 | TGCGGCAGGAGCAGA[C/T]TGACAATCAGTAAGG | 6709 |
rs765814431 | snp | A/G | 1.65367e-05 | 0.00287543 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591642 | TAAGGATGACACTGG[A/G]GGCCGCAAGGGCTAG | 6709 |
rs765818630 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566137 | TGATGGCTCACTGCA[G/T]TCTTGAACTCCTGGG | 6709 |
rs765830586 | snp | C/T | 1.64901e-05 | 0.00287137 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128581041 | TGAGCAGGTGGACAA[C/T]TGGATGAGCAAGCAG | 6709 |
rs765853252 | snp | A/C/T | 0.000106219 | 0.00728696 | downstream-variant-500B, utr-variant-3-prime | SPTAN1, WDR34 | GRCh38.p7 | 9:128633714 | CAAGGCTCGGCACAG[A/C/T]GAAGGCTTGCACCCG | 6709 |
rs765859324 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570131 | TTCCTTGATAGAAGT[C/T]GTTTTCCCAGAGTGA | 6709 |
rs765870145 | snp | C/G | 1.7141e-05 | 0.0029275 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609321 | TTGGTCTTGATGTAG[C/G]CTTATGTTATTGAGT | 6709 |
rs765876891 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611648 | CTGCCTCTGAGAACC[C/T]CTTCCCCCTGAAAAG | 6709 |
rs765881182 | snp | C/T | 1.67854e-05 | 0.00289697 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626010 | GTGAAGCTTAGCTGG[C/T]CCACAGCTCAAGGAA | 6709 |
rs765946226 | snp | A/G | 1.64808e-05 | 0.00287057 | missense | SPTAN1 | GRCh38.p7 | 9:128611793 | GGGTTATCGACATGG[A/G]CAACTCCCTCATTGA | 6709 |
rs765985014 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577719 | ACTTCATAAATTCTT[C/T]TATTCTGCATCACTG | 6709 |
rs766025318 | snp | A/G | 1.66316e-05 | 0.00288367 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585704 | GTCCTTCTGTGATGT[A/G]TCAACGTAGTTTTTG | 6709 |
rs766038302 | snp | G/T | | | missense | SPTAN1 | GRCh38.p7 | 9:128625907 | TCCCTCATGAAGAGG[G/T]GGAGCCAGCTTCTGG | 6709 |
rs766040138 | snp | A/C | 0.000103215 | 0.0071831 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611681 | ATAACCTAGCAGGAA[A/C]TGGTTTGGAAAAAAT | 6709 |
rs766043087 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603722 | CTATTGGGTCCAAGC[A/G]TGTCCTAAGTAAACA | 6709 |
rs766045686 | snp | A/G | 1.7243e-05 | 0.00293619 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576796 | AGAAGTTGTGTACAA[A/G]TCCAGTCTCTTCTCT | 6709 |
rs766064385 | snp | C/G/T | 4.95531e-05 | 0.0049774 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632516 | TCGCCCTGGCTGGGT[C/G/T]GGGGGTGTTCGGCAG | 6709 |
rs766086907 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578918 | GTCAAACATGTTTCT[C/T]TACACTAGCAACAGA | 6709 |
rs766111201 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624509 | ACTGTCAGCAAGGCC[C/G]GGAAGAGCCTTCCCA | 6709 |
rs766122940 | snp | A/C/G | 3.30957e-05 | 0.0040678 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566721 | GGTACTTATCTCAGC[A/C/G]CATTTTGTCATTTCA | 6709 |
rs766126763 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610728 | ACCATATCAGGCGCC[C/G]AGGATCAGGAGCCCA | 6709 |
rs766133425 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559053 | CACAAATGAAAATTC[C/T]GAATGCTGACTGCAG | 6709 |
rs766141611 | snp | A/G | 3.30387e-05 | 0.00406427 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128566881 | TTCCTATCGATTCCA[A/G]TTCTTTCAAAGAGAT | 6709 |
rs766144097 | snp | A/G | 0.000124154 | 0.00787792 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628135 | TGGTCCCTGGTCCCC[A/G]ATAGAGCCTTCAAGC | 6709 |
rs766158980 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592515 | CCTGACCTCGTGATC[C/T]GCCCGCCTTGGCCTC | 6709 |
rs766187559 | snp | A/G | 1.64931e-05 | 0.00287163 | missense | SPTAN1 | GRCh38.p7 | 9:128613451 | ACCTGCTGAAAAAGC[A/G]TCAACTGCTGGAAGC | 6709 |
rs766194537 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570694 | GGAGTTTTGCTCTTG[G/T]TGCCCCGGCTGGAGT | 6709 |
rs766194986 | snp | C/T | 3.67195e-05 | 0.00428467 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592935 | TTTCATCCCTGTGGA[C/T]TAACCCCACTAATTC | 6709 |
rs766229112 | snp | C/G | 3.88131e-05 | 0.00440512 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628191 | GGGCGATTCCAAGGG[C/G]TCACTTTGGGTAGGG | 6709 |
rs766229911 | snp | C/G | 1.6676e-05 | 0.00288751 | missense | SPTAN1 | GRCh38.p7 | 9:128632919 | GGCCCTCAGCTCAGA[C/G]GGAAAGCCTTACGTG | 6709 |
rs766238221 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583426 | CCTGTGTAGGAATTA[C/T]TTGGCTTAAGTTCTT | 6709 |
rs766258097 | in-del | -/G | 1.76585e-05 | 0.00297135 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588993 | CGCTGGCACCTCCAC[-/G]TATGCTCAGTTGGGT | 6709 |
rs766264348 | in-del | -/A | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559432 | ATTTCTGTAGCAGGT[-/A]AAAGGATTTTAGAAA | 6709 |
rs766271485 | snp | A/G | 1.64773e-05 | 0.00287026 | missense | SPTAN1 | GRCh38.p7 | 9:128583911 | GCAAAGATCTTACCA[A/G]TGTGCAGAACCTCCA | 6709 |
rs766273505 | snp | A/C/G | 1.65124e-05 | 0.00287331 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583758 | GGGTAATGCTAAGCA[A/C/G]TACAAAATTAAACTT | 6709 |
rs766313282 | snp | A/C | 1.65622e-05 | 0.00287764 | missense | SPTAN1 | GRCh38.p7 | 9:128577454 | ATTACAAACTGGGAG[A/C]AGATCCGCACCTTGG | 6709 |
rs766361381 | snp | C/T | 1.69321e-05 | 0.0029096 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587722 | GTAACAGTTTATGGG[C/T]TACTGGAGGGAGGCC | 6709 |
rs766361461 | in-del | -/AGCTTTTCTGGAGATCAAAC | 1.71211e-05 | 0.00292579 | downstream-variant-500B, frameshift-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128633950 | CTGTGGGTTTCTGGG[-/AGCTTTTCTGGAGATCAAAC]AGCTGCACGTCACCT | 6709 |
rs766361565 | snp | G/T | 1.6516e-05 | 0.00287362 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583752 | GCAGAAGGGTAATGC[G/T]AAGCAGTACAAAATT | 6709 |
rs766362867 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608486 | AAAATATTATCAAAG[C/G]GATGGAAAACAAATG | 6709 |
rs766370044 | snp | C/T | | | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128550695 | AAGGTGCTTTCTTTG[C/T]TGGAGCAGAAGGTCT | 6709 |
rs766372742 | snp | A/G | 5.15743e-05 | 0.00507784 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604443 | AGCCCTGGGCTGGGA[A/G]AGGGAGAAACAGGTG | 6709 |
rs766385606 | snp | G/T | 1.65633e-05 | 0.00287774 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608855 | CCCACCTTGATCTCA[G/T]GCCTTTGTTTTCTGA | 6709 |
rs766409577 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615490 | TGAAAATAGTGTGAG[C/T]TGATAGAATGCCAGA | 6709 |
rs766446488 | in-del | -/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602934 | AGCCAGCATGCCTAG[-/C]CCTAAGGGACTTTAG | 6709 |
rs766452202 | snp | C/G | 1.6473e-05 | 0.00286988 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612281 | CTTCCTACCAGTGGG[C/G]GATTTCTAGTCATTT | 6709 |
rs766460093 | snp | A/G | 3.25887e-05 | 0.00403649 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594421 | TGTTTAAAGATTTGA[A/G]TCTCTTGATTTTTTT | 6709 |
rs766471063 | in-del | -/GTG | | | cds-indel | SPTAN1 | GRCh38.p7 | 9:128578201 | GAGCTTGCCAGTGAT[-/GTG]GCTGGGGCTGAAGCC | 6709 |
rs766479818 | snp | C/T | 1.64874e-05 | 0.00287113 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128605397 | AAACCAGGCCTGGAG[C/T]AGCCTGGGGAAACGT | 6709 |
rs766488215 | in-del | -/A | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624831 | GCTCCTGGGTGAGGG[-/A]AAAACTGGGTCCGGA | 6709 |
rs766491965 | snp | A/G | 4.95855e-05 | 0.00497899 | missense | SPTAN1 | GRCh38.p7 | 9:128584510 | AAAGAGCCCATTGCC[A/G]CATCTACCAACAGAG | 6709 |
rs766529811 | snp | A/G | 1.67947e-05 | 0.00289777 | missense | SPTAN1 | GRCh38.p7 | 9:128621234 | ATGATGTCTGCACCA[A/G]TGGACAAGACCTCAT | 6709 |
rs766550915 | snp | A/C | 1.70441e-05 | 0.0029192 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632154 | GAAATCCGAGCCATG[A/C]GAAGTCAGCTCAAAA | 6709 |
rs766566121 | snp | A/G | 1.70441e-05 | 0.0029192 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609315 | TGGGTGTTGGTCTTG[A/G]TGTAGCCTTATGTTA | 6709 |
rs766568389 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593373 | CTTAGTAGGAAGGAA[A/G]TCATATGCTTCTCTT | 6709 |
rs766608970 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614568 | GTATTCCAGCCTGGG[C/T]GACAGAATGAGACTA | 6709 |
rs766616293 | snp | A/G | 0.000247854 | 0.0111295 | missense, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633260 | CACATGAAGCCCTAC[A/G]TGGACGGCAAGGGCC | 6709 |
rs766617537 | snp | A/G | 0.000247555 | 0.0111228 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627013 | AGACAGGGTGTTGCT[A/G]TGTTGCCCAGGCTGG | 6709 |
rs766620145 | snp | C/T | 1.64808e-05 | 0.00287057 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128625116 | AGGTGAAAAGGAGAA[C/T]AGCTTGAAGACAGAT | 6709 |
rs766673044 | snp | A/G | 8.28246e-05 | 0.00643471 | missense | SPTAN1 | GRCh38.p7 | 9:128583158 | CAGAGCCGAATTGAT[A/G]CCTTGGAGAAAGCTG | 6709 |
rs766688827 | snp | A/G | 1.64781e-05 | 0.00287033 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582600 | CTTTTTGGTACATGA[A/G]TGTCTCTTCTAAGAT | 6709 |
rs766693290 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606915 | TAGTTTTGGAACATT[C/T]TCATTGCCCTAGAAT | 6709 |
rs766711939 | snp | A/C | 1.64819e-05 | 0.00287066 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628026 | TGGCTTGTGGAGGAT[A/C]CCGGGATGGGCCTTC | 6709 |
rs766776503 | snp | C/G | 1.64817e-05 | 0.00287064 | missense | SPTAN1 | GRCh38.p7 | 9:128582503 | GAATTTGCAACCAAG[C/G]TAATTCAGAACAACC | 6709 |
rs766776858 | in-del | -/A | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590550 | TCTATTTATATTAAA[-/A]AAAGAAAAAAAAAAA | 6709 |
rs766779966 | in-del | -/TG | 8.25655e-05 | 0.00642463 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617614 | GGTGCAGAGACTGAC[-/TG]TGCTGTTTCCCATCT | 6709 |
rs766790804 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575484 | TGAGAGTTTTGTTTA[G/T]ATGTGAGGCACAATA | 6709 |
rs766792989 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563213 | TTGAGTCCAGGAGTT[C/T]GAGACTAGCCTGGGC | 6709 |
rs766802455 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621392 | CCAGCAGCAATTCCA[G/T]TCCTGTGTTTCGTGA | 6709 |
rs766824948 | snp | C/G | 1.68218e-05 | 0.00290011 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128624480 | GGACGTGGTGGAGTC[C/G]TGGATCGGTGAGCAC | 6709 |
rs766843757 | snp | A/G | 0.000120732 | 0.00776863 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588982 | TGTTTGTTCCACGCT[A/G]GCACCTCCACGTATG | 6709 |
rs766849839 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620305 | GGGAAGCATCCTCCC[A/G]CTGGTCAGGGTGATT | 6709 |
rs766860881 | snp | A/C | 1.64754e-05 | 0.00287009 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128574737 | GATGCGAGAAAAAGG[A/C]ATCAAACTGCTGCAG | 6709 |
rs766883905 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564023 | TACACCTGTAATCTT[A/G]GCACTTTGGAAGACC | 6709 |
rs766886425 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586528 | ACATTTGTCACTCTT[A/G]TTTCATCTATGTGAA | 6709 |
rs766916217 | snp | A/G | 1.64732e-05 | 0.0028699 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603636 | CCCCTGGTTTTCTCC[A/G]CTATCTTCCTTCCCT | 6709 |
rs766922699 | snp | G/T | 1.64746e-05 | 0.00287002 | missense | SPTAN1 | GRCh38.p7 | 9:128609226 | AGATTGAGGCTTGGA[G/T]CAGTGAAAAATTGCA | 6709 |
rs766924448 | snp | G/T | 4.95471e-05 | 0.00497705 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128617721 | GAAGAAGCACAAGCG[G/T]CTGGAAGCAGAACTG | 6709 |
rs766927132 | snp | C/T | 0.000115669 | 0.00760402 | synonymous-codon, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633301 | CACCGCGTTCGACTA[C/T]GTGGAGTTCACCCGC | 6709 |
rs766946262 | in-del | -/G | 1.69433e-05 | 0.00291056 | downstream-variant-500B, frameshift-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128633909 | CAGTAGACAGGGCTT[-/G]TCATCCTGGGTTTGC | 6709 |
rs766960383 | snp | A/G | 7.33972e-05 | 0.00605749 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583313 | TGAATTGTGACATGC[A/G]TGTTTGGGGAACTAA | 6709 |
rs766986604 | snp | C/T | 1.64808e-05 | 0.00287057 | missense | SPTAN1 | GRCh38.p7 | 9:128583881 | TAGAAGGTCACTTGG[C/T]TTCGGATGATTACGG | 6709 |
rs767012741 | snp | A/G | 1.65111e-05 | 0.0028732 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617620 | GAGACTGACTGTGCT[A/G]TTTCCCATCTCTCAT | 6709 |
rs767056326 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602441 | AGGCTGGTATTGATC[G/T]CCTAACCTCACCTGA | 6709 |
rs767057757 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574875 | AGGGAAGAGACTCCT[C/T]TGTGATCTGTAGTGA | 6709 |
rs767067922 | snp | A/G | 8.24708e-05 | 0.00642095 | missense | SPTAN1 | GRCh38.p7 | 9:128580937 | CTGACCGTCCTTTCC[A/G]AGGAGAGAGCGGCGC | 6709 |
rs767082746 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565369 | GTTTCCTTTTATAGT[A/G]TAAAACATTTTGGAC | 6709 |
rs767084828 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622817 | GAGTGCACTGGCGCA[A/G]TCTCACCTCACTGCC | 6709 |
rs767100168 | snp | C/T | 3.29717e-05 | 0.00406015 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617966 | CTACCTGCTGTTAAC[C/T]TCCTCGTCCTTGCCT | 6709 |
rs767158342 | snp | C/G | 1.65102e-05 | 0.00287312 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591631 | TTGACAATCAGTAAG[C/G]ATGACACTGGGGGCC | 6709 |
rs767171688 | in-del | -/TCC | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128555621 | AAATTTGCAAAGCCT[-/TCC]TTTTTTTTTTTTTTT | 6709 |
rs767175912 | snp | C/T | 0.000132004 | 0.0081231 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128608270 | TGACAAAGCGATTAA[C/T]GTCCAGGTGAGGCCT | 6709 |
rs767231674 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588342 | TTGAGATGGAGTTTC[A/G]CTCTTGTTGCCCAGG | 6709 |
rs767246459 | snp | A/T | 1.648e-05 | 0.0028705 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577000 | TGGGTCTCAACCTGG[A/T]GGGGAGTTGTGAAGC | 6709 |
rs767265808 | snp | C/T | 1.64863e-05 | 0.00287104 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128581014 | GGACCTGCAGCTCTT[C/T]TACCGGGACACTGAG | 6709 |
rs767275278 | snp | G/T | 1.64732e-05 | 0.0028699 | missense | SPTAN1 | GRCh38.p7 | 9:128618910 | GGAATATCAGCAGTT[G/T]GTAGCCAATGTGGAA | 6709 |
rs767276957 | snp | A/C | 1.64727e-05 | 0.00286986 | missense | SPTAN1 | GRCh38.p7 | 9:128577253 | GGTCTGGAGAGAGAT[A/C]TTGCTGCTCTAGAAG | 6709 |
rs767301092 | snp | A/G | 1.65048e-05 | 0.00287265 | missense | SPTAN1 | GRCh38.p7 | 9:128632690 | GACCCTGAGTTCGAG[A/G]CAATCCTGGACACGG | 6709 |
rs767309611 | snp | C/T | 3.30868e-05 | 0.00406723 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619051 | CTCTCTTGGCAACTG[C/T]CTGCTGGTCATCATT | 6709 |
rs767310956 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618406 | AATCAAGACATGAGA[A/G]TCTGGAATCACAGAG | 6709 |
rs767352041 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128556589 | TTTCTCAATATTGCT[C/G]TGCATTTCTGGATTT | 6709 |
rs767367080 | snp | A/G | 1.65299e-05 | 0.00287483 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632785 | GCCCTCCCTGCTCAG[A/G]CTCTTGCTTCCCCCG | 6709 |
rs767370900 | in-del | -/A | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590547 | ATCTCTATTTATATT[-/A]AAAAAAGAAAAAAAA | 6709 |
rs767387665 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581134 | TCGGGTAGTGTGCTT[A/G]TTTTGTTTTAGGACA | 6709 |
rs767399516 | snp | C/T | 8.79562e-05 | 0.00663101 | missense | SPTAN1 | GRCh38.p7 | 9:128626614 | AGAGCTTCCGCGTAG[C/T]CTCCAACCCCTACAC | 6709 |
rs767424166 | in-del | -/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610559 | ACTGCCTTTTAGTTG[-/T]TTTTTTTTTTGCCCC | 6709 |
rs767431284 | snp | C/T | 6.63614e-05 | 0.00575989 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566704 | CTATTTTGGTGCCTA[C/T]TGGTACTTATCTCAG | 6709 |
rs767437952 | in-del | -/G | 9.48578e-05 | 0.00688621 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579766 | AAATGGAGCTTTTGA[-/G]GAGCAAATTACACCT | 6709 |
rs767443717 | snp | A/G | 6.59348e-05 | 0.00574135 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128582490 | CTAGGCATTAGATGA[A/G]TTTGCAACCAAGCTA | 6709 |
rs767451067 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593200 | CTCACAAGGGAAGAG[A/G]TCGCGGTGCAGCTGT | 6709 |
rs767460630 | snp | A/G | 1.66407e-05 | 0.00288446 | missense | SPTAN1 | GRCh38.p7 | 9:128583215 | TATGCCAAGGATGAA[A/G]TGGCAGCTCGTATGA | 6709 |
rs767468489 | snp | C/G | 1.72502e-05 | 0.0029368 | downstream-variant-500B, intron-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128633998 | CTGCAAAGAGAGACA[C/G]ATACGTGGAGTAAGA | 6709 |
rs767470484 | in-del | -/A | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606486 | CATATATATATATAT[-/A]ATTTTTTTTTTGGGG | 6709 |
rs767495066 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627146 | CAGTCCAGCAACTCC[C/G]TGCTTGACTGACCAG | 6709 |
rs767504664 | snp | A/G | 1.689e-05 | 0.00290598 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594390 | TATGGGCAGTCTTCA[A/G]GCTCAGCTGAAAATT | 6709 |
rs767505153 | snp | A/G | 6.59055e-05 | 0.00574007 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128608228 | ACTGGACAGCGTAGA[A/G]GCTCTGATCAAAAAA | 6709 |
rs767505478 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614315 | ACAAAAATTAGGCTG[C/G]GCATGGTGAGTCATG | 6709 |
rs767505862 | snp | C/G | 1.65081e-05 | 0.00287293 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628041 | CCCGGGATGGGCCTT[C/G]CTGCCCAGGGCGGGC | 6709 |
rs767513681 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128633097 | TATGGACAGAAGTCC[C/T]GGATCTGCTTGTAGA | 6709 |
rs767527240 | snp | C/T | 1.64776e-05 | 0.00287028 | missense | SPTAN1 | GRCh38.p7 | 9:128574724 | TACTTTTGGAGAAGA[C/T]GCGAGAAAAAGGAAT | 6709 |
rs767550664 | snp | A/G | 3.29511e-05 | 0.00405887 | missense | SPTAN1 | GRCh38.p7 | 9:128582704 | TTCAGCTGTTGAGCC[A/G]CCGCAATGCCCTTCA | 6709 |
rs767551759 | in-del | -/C | 1.6777e-05 | 0.00289624 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613505 | GCAAAGGGAGGCGGG[-/C]CAGGCCCGAGTGCCT | 6709 |
rs767610379 | in-del | -/TCCTC | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584185 | AGATAGCAGAAAGAA[-/TCCTC]TCAGGAATGGAAAAA | 6709 |
rs767610692 | snp | A/G | 1.64895e-05 | 0.00287132 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128581892 | GGAGGAAAAGATTAC[A/G]GTAAGACCCCTTCTT | 6709 |
rs767617004 | snp | A/C/G | 6.59287e-05 | 0.00574113 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568924 | TAGCTCGTGGAGTGG[A/C/G]TGGCTTCATCTGGGT | 6709 |
rs767620941 | snp | A/C | 1.65312e-05 | 0.00287495 | missense, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633254 | GTCTCCCACATGAAG[A/C]CCTACGTGGACGGCA | 6709 |
rs767640999 | snp | C/T | 8.24926e-05 | 0.0064218 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128626516 | AATCAAAGCTTTGCG[C/T]GAGGCCCACGACGCC | 6709 |
rs767657282 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624700 | TGGCACCAGGGTCAA[G/T]AAACAAAAGCCTGTA | 6709 |
rs767666209 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620246 | GGAAGCAGGAGTGTG[A/C]ACTCCCAGGAATCGA | 6709 |
rs767678599 | snp | A/G | 4.94752e-05 | 0.00497344 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128605367 | AGAAGACCTGCAGGA[A/G]AAGTGCACAGAGTTA | 6709 |
rs767679923 | snp | A/G | 3.29468e-05 | 0.00405861 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128609188 | ATCTCAAACCCTCCA[A/G]CAGTTCAGCCGGGAT | 6709 |
rs767701707 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627737 | TCCCGGATTGAGTGG[A/G]ACCATGCAGGGCGCG | 6709 |
rs767728151 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626058 | CTGCCCAGCTCTGCC[A/G]CTCCCCCTTGAGGAA | 6709 |
rs767768465 | snp | A/G | 8.24872e-05 | 0.00642159 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605229 | TTTGCCCCAGAAAGA[A/G]CAGAGTCTTCTGTTC | 6709 |
rs767771821 | snp | G/T | 1.64779e-05 | 0.00287031 | missense | SPTAN1 | GRCh38.p7 | 9:128607907 | AGGCATTTGAGCAGT[G/T]TGGACAGCAGCTGTT | 6709 |
rs767815914 | snp | A/C/G | 3.30498e-05 | 0.00406497 | synonymous-codon, missense | SPTAN1 | GRCh38.p7 | 9:128584500 | GATTCGAGAGAAAGA[A/C/G]CCCATTGCCGCATCT | 6709 |
rs767918528 | snp | C/T | 1.65321e-05 | 0.00287502 | missense | SPTAN1 | GRCh38.p7 | 9:128584391 | TGGCTCGCTATGAGG[C/T]ACTCAAGGAGCCCAT | 6709 |
rs767919324 | snp | A/G | | | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128552288 | GCCAGGGCGTAGGCA[A/G]TGACCTCACTGCACC | 6709 |
rs767937125 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616030 | TAATTGGCGGTGGTG[A/G]TGATCCATGCTGGCT | 6709 |
rs767942809 | in-del | -/GC | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574974 | TGCTCTCTAGGTGTA[-/GC]TGTGCTATTCTGTAA | 6709 |
rs767958437 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629733 | TCTAGAGGATGGAAC[C/T]GGGATCTGGGGTTTA | 6709 |
rs767960483 | snp | C/T | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554695 | CAGCTGCGGCTGTAC[C/T]GTAGAAGAATGCAAC | 6709 |
rs767967588 | snp | C/T | 3.29451e-05 | 0.00405851 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627899 | CACCACCTTGTCTCC[C/T]GGCTGCTTGGATCTG | 6709 |
rs767974935 | snp | C/T | 4.96915e-05 | 0.0049843 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582867 | AATGTACTGTTAGTG[C/T]TGCCATGTAGCACTC | 6709 |
rs767995880 | snp | C/T | 1.6727e-05 | 0.00289193 | intron-variant, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633178 | TGGGTGCAGCTGGCT[C/T]AGGCACCAGGTGCCA | 6709 |
rs768027782 | in-del | -/CTTC | 0.000164742 | 0.00907435 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578090 | CTGGAAACATAATGT[-/CTTC]CTTTGGTTTTCCCTA | 6709 |
rs768031366 | snp | A/G | 1.64814e-05 | 0.00287061 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600157 | TTTCAAGAGTTTTGC[A/G]AGATCATGAAATATG | 6709 |
rs768062334 | snp | C/T | | | intron-variant, missense | SPTAN1 | GRCh38.p7 | 9:128629138 | AGCATAGCATATCGT[C/T]GGGTCATTCGTGTCT | 6709 |
rs768065593 | snp | A/G | 2.53322e-05 | 0.00355885 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627518 | CAGCCCGCTGGGGCC[A/G]GGGAGCAGCAGCATG | 6709 |
rs768081397 | in-del | -/TTTC | 1.64808e-05 | 0.00287057 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598922 | CTTGAGAGATGTGTA[-/TTTC]TTCTAATAATAAAAC | 6709 |
rs768098501 | snp | C/G/T | 3.29708e-05 | 0.00406011 | missense | SPTAN1 | GRCh38.p7 | 9:128588863 | CTGGTCTTGGCTCTC[C/G/T]ACGACTATCAGGAGA | 6709 |
rs768103982 | snp | C/G | 1.65247e-05 | 0.00287438 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632759 | TGAGCCTCTGCCCGG[C/G]GCACCCACCTGCCCT | 6709 |
rs768104125 | snp | C/T | 1.64849e-05 | 0.00287092 | missense | SPTAN1 | GRCh38.p7 | 9:128577398 | TGCAACAGTCCCACC[C/T]TCTGAGTGCAACACA | 6709 |
rs768107932 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602100 | GACAGTGGGTCCACC[C/T]TCTGACTCCTATAAA | 6709 |
rs768119148 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598211 | CTTGGGCCTCCCAAA[G/T]TGCTGGGATTACAGG | 6709 |
rs768154577 | snp | A/G | 1.65773e-05 | 0.00287895 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608825 | CTGGCAGTCCAGGCA[A/G]GGCCCAGCCACAGGC | 6709 |
rs768161923 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611656 | GAGAACCCCTTCCCC[C/G]TGAAAAGACATAACC | 6709 |
rs768166158 | snp | A/G | 1.66977e-05 | 0.00288939 | missense | SPTAN1 | GRCh38.p7 | 9:128624455 | CCTTCCTTCAGTTCA[A/G]CTGGAAGGCGGACGT | 6709 |
rs768169689 | snp | G/T | 1.64743e-05 | 0.00287 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607586 | TAATAGCTATTTTTC[G/T]GGGGTGCTGGTTTCC | 6709 |
rs768183025 | snp | C/T | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554314 | GATTCTCTGATATGC[C/T]TTGGTCTTGGCAGTG | 6709 |
rs768195496 | snp | A/T | 1.65776e-05 | 0.00287898 | missense | SPTAN1 | GRCh38.p7 | 9:128632882 | ACGTCAAGTCCAGCG[A/T]GGAGATTGAGAGCGC | 6709 |
rs768225874 | snp | A/G | 3.29794e-05 | 0.00406061 | missense | SPTAN1 | GRCh38.p7 | 9:128594329 | GTCGGAGCAGACTTG[A/G]AGCAGGTTGAGGTGC | 6709 |
rs768243872 | in-del | -/A | 1.64768e-05 | 0.00287021 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584851 | GGAGGAAGGTGAGTG[-/A]TTGGTATCAGTGACA | 6709 |
rs768252290 | snp | A/T | 1.64773e-05 | 0.00287026 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582588 | TTCATGCTCCTCCTT[A/T]TTGGTACATGAATGT | 6709 |
rs768271102 | snp | A/G | 4.95872e-05 | 0.00497907 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128584482 | TGAGGATGAGGAGAC[A/G]TGGATTCGAGAGAAA | 6709 |
rs768276579 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568566 | ACCATTGATGGCCCT[C/T]GCTGGCCAGGCTTTC | 6709 |
rs768278537 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571324 | GCACAGTGGCTCATG[C/T]CTGTAATCCTAGCAC | 6709 |
rs768280253 | snp | A/T | 3.31131e-05 | 0.00406884 | missense | SPTAN1 | GRCh38.p7 | 9:128621165 | TACTCCAGGGCTTAC[A/T]GAAGAAACATGAAGC | 6709 |
rs768283186 | snp | G/T | 0.00133755 | 0.025826 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566988 | TGCAGGTACGTCTGA[G/T]CTCCTGGGATTCCTG | 6709 |
rs768287672 | snp | A/G | 1.64838e-05 | 0.00287083 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574835 | GTTTTGGGAAGAAGG[A/G]TTTGCTAAGCTTTAC | 6709 |
rs768293591 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629457 | TTTGAACCTGGGGAG[A/G]TTGCAGAGCTAACCC | 6709 |
rs768294119 | snp | C/T | 1.67497e-05 | 0.00289389 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128577498 | TGCACGGCTCAATGA[C/T]TCATACAGGTGCAAA | 6709 |
rs768299032 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627800 | GATGCAGGGTCTGTG[C/T]GTTGGGTACTGATGT | 6709 |
rs768302291 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615213 | GTCTGAATGAGCATA[A/G]TTTGTTCGGTGGTTG | 6709 |
rs768305579 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578675 | CTCTACTAAAAATGC[A/G]ACAGTTAGCTGGTCA | 6709 |
rs768310260 | snp | C/T | 2.03938e-05 | 0.00319319 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632111 | GTCTGAGCATCTGTG[C/T]TCCCCACCCCTGCAG | 6709 |
rs768322079 | snp | C/T | 1.64942e-05 | 0.00287173 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128617691 | CCGGGACCTAACCGG[C/T]GTGCAGAACCTGAGG | 6709 |
rs768377240 | snp | C/T | 3.30142e-05 | 0.00406276 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580882 | TCGGAGGCATTGGGG[C/T]TGACCTCATCTCCCT | 6709 |
rs768382412 | snp | C/T | 5.06017e-05 | 0.00502974 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613518 | GGCCAGGCCCGAGTG[C/T]CTGGGACACAGCTCT | 6709 |
rs768426112 | snp | A/C/G/T | 4.96319e-05 | 0.00498138 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587586 | CCTGCACAGTGCTCC[A/C/G/T]TGTGTGGTTTTGGTT | 6709 |
rs768426829 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564495 | GGCTGAGGTGGAAGC[A/G]TCACTTGAACCAGGG | 6709 |
rs768426868 | snp | A/G | 1.64732e-05 | 0.0028699 | missense | SPTAN1 | GRCh38.p7 | 9:128609157 | AGATGATTGAGAAAA[A/G]GTCAAAGCTAGGAGA | 6709 |
rs768426871 | in-del | -/G | 1.68635e-05 | 0.0029037 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632968 | CAGGTATGGGCCTCA[-/G]GAGGTGGGTGAAGAG | 6709 |
rs768430374 | in-del | -/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591845 | ACCAGTGTTCATGAG[-/T]TTTTCCTAACCAGAA | 6709 |
rs768463272 | snp | A/C | 1.65351e-05 | 0.00287528 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582459 | GCTTACCAATGAAGA[A/C]CTCTTATCTTCCTTC | 6709 |
rs768467017 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595894 | TGTTGCCCAGGCTGG[A/G]GTGCAGTGGCCCAGT | 6709 |
rs768470278 | snp | C/T | 1.66751e-05 | 0.00288744 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624284 | ATAGTCAGGTAACCA[C/T]AGCAGGTAAGGCTGA | 6709 |
rs768474357 | snp | C/T | 1.64825e-05 | 0.00287071 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128613393 | CAGGTGGAGGCCCTG[C/T]TGGCATCCGAAGATT | 6709 |
rs768474578 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569926 | ATGATGAATAATTAT[C/T]AACTATTACTAATAA | 6709 |
rs768483935 | in-del | -/AGGACATTTGCAA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619676 | ATCTTACCTTTGCAG[-/AGGACATTTGCAA]AGATCTTGTTTCCAC | 6709 |
rs768500975 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | SPTAN1 | GRCh38.p7 | 9:128591553 | AATTGGACCCCGCCC[A/G]GTCAGCCTCCCGGGA | 6709 |
rs768529983 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621132 | AGCAGGCTCTCAATA[C/G]TGTGCCTTGGCTGCT | 6709 |
rs768532064 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128596674 | TCCTATAGTAACTGT[C/G]CATTAAAATTTTATC | 6709 |
rs768538310 | snp | A/T | 1.64825e-05 | 0.00287071 | missense | SPTAN1 | GRCh38.p7 | 9:128574691 | CCCGTTTGATGGAGC[A/T]GCACCGCCAGTGGGA | 6709 |
rs768542176 | snp | C/T | 3.30759e-05 | 0.00406655 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128605469 | GCAGCGCTTCCTTAG[C/T]GATTTCCGGTACGGA | 6709 |
rs768594714 | snp | A/T | 1.64727e-05 | 0.00286986 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591463 | ACTTTCAGTTCTCCC[A/T]CTTTTTTCCTTAGGA | 6709 |
rs768606839 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582102 | ATGGAAACCTCCAAA[A/C]TTCTTTAAGTTTGTA | 6709 |
rs768619495 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563881 | GGGCTCAAGCAATCC[A/G]CCCACCTCAGCCTCC | 6709 |
rs768619719 | snp | C/T | 1.65051e-05 | 0.00287267 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128609278 | CAAGGATCCCACCAA[C/T]ATCCAGGTAAGCTGA | 6709 |
rs768665374 | snp | A/G | 1.67379e-05 | 0.00289287 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632267 | CCAGCAGTGGGACCA[A/G]CTGGACCAGCTGGGC | 6709 |
rs768716077 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586983 | CCACCACGCCCAGCT[A/G]ACTTTTTTTGTATTT | 6709 |
rs768756400 | snp | C/T | 1.65603e-05 | 0.00287747 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582861 | TAAAGTAATGTACTG[C/T]TAGTGTTGCCATGTA | 6709 |
rs768756536 | snp | C/T | 1.64887e-05 | 0.00287125 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128585920 | GCGGGAGAAGGAACC[C/T]ATTGTGGGCAGCACT | 6709 |
rs768791824 | snp | C/T | 3.29462e-05 | 0.00405857 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128612129 | CCTGGCTGCCTTAGC[C/T]GACCAGTGGCAGTTC | 6709 |
rs768804390 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575405 | AACTTTTTAGTATAT[G/T]CAGGATAAAATTTTG | 6709 |
rs768855213 | snp | C/T | 3.43778e-05 | 0.00414581 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615883 | CCCTTACGCCTGTAA[C/T]AGTGGGCAGCAGGAA | 6709 |
rs768910504 | snp | C/G | 1.68584e-05 | 0.00290326 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579606 | GTAAGATGCTGGGCA[C/G]AAATCATGGCTTTGT | 6709 |
rs768911375 | snp | A/G | 1.64961e-05 | 0.00287189 | missense | SPTAN1 | GRCh38.p7 | 9:128632619 | ACCATCAGGAGTTCA[A/G]ATCTTGCCTGCGCTC | 6709 |
rs768919498 | snp | A/G | 4.94173e-05 | 0.00497053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627893 | TCCGGACACCACCTT[A/G]TCTCCCGGCTGCTTG | 6709 |
rs768925077 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567892 | CAGCCTCCCGAGTAG[C/T]TGGGAATGTAGGCAC | 6709 |
rs768933627 | snp | C/T | 1.65302e-05 | 0.00287486 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581104 | TGGGAGAAGAAGGGC[C/T]TGTGTTTTGCCTCCT | 6709 |
rs768940761 | snp | A/G/T | 6.59646e-05 | 0.00574269 | missense | SPTAN1 | GRCh38.p7 | 9:128580946 | CTTTCCGAGGAGAGA[A/G/T]CGGCGCTGCTGGAGC | 6709 |
rs768953216 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610117 | GGCATCCAGAGGTGC[C/T]AGTCAGGAGAGGAAC | 6709 |
rs768968917 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599238 | CTCCCAGGTTCAAGC[A/G]ATTCTCCCATCTCAG | 6709 |
rs768972771 | snp | A/G | 1.64727e-05 | 0.00286986 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603603 | AAGGTAAGAAGCAGT[A/G]ACCAGCTCCTCTGAT | 6709 |
rs768986492 | snp | C/T | | | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128624402 | AGACCTGGAGAAAGC[C/T]GCAGCCCAGAGAAAG | 6709 |
rs768999930 | snp | A/G | 8.26358e-05 | 0.00642737 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626369 | CTGGCGACTCCGCCA[A/G]CTCAGTCTCTTCTGC | 6709 |
rs769008515 | snp | C/T | 4.94173e-05 | 0.00497053 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128581787 | CTTTGGCAAGGCGTT[C/T]CTGTTGAATGAAGAC | 6709 |
rs769025158 | snp | C/T | 3.11105e-05 | 0.00394389 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593084 | CACCAATGTCCACTG[C/T]TACCCTATCCATTCT | 6709 |
rs769045630 | snp | C/T | 0.000170271 | 0.00922531 | downstream-variant-500B, synonymous-codon | SPTAN1, WDR34 | GRCh38.p7 | 9:128633924 | TTCATCCTGGGTTTG[C/T]TTGATCAAAACTGTG | 6709 |
rs769058539 | snp | G/T | 0.000131804 | 0.00811695 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600140 | CCTTTGCAAATTATT[G/T]TTTTCAAGAGTTTTG | 6709 |
rs769059325 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628902 | TCCGTGAGGTGCCAC[A/G]CTCCCCTCACCTTAT | 6709 |
rs769061614 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567112 | TAAGGAAGGACAAAC[C/T]CATTGTTTTCCTGTA | 6709 |
rs769062571 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600375 | GCTGCAGCAGGGAGC[A/G]CTGTTGTTGGCAGGG | 6709 |
rs769081903 | snp | A/G | 1.64912e-05 | 0.00287147 | missense | SPTAN1 | GRCh38.p7 | 9:128605170 | GACCTTGCGGCTCTC[A/G]GTGACAAGGTGAGAG | 6709 |
rs769085429 | snp | C/T | 1.7327e-05 | 0.00294333 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576786 | TGGAGGAGCCAGAAG[C/T]TGTGTACAAATCCAG | 6709 |
rs769094437 | snp | A/C | 0.00120403 | 0.0245065 | missense | SPTAN1 | GRCh38.p7 | 9:128584321 | CAGGCCCGCCAGTTC[A/C]AAGATGCTGGCCATT | 6709 |
rs769095281 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612622 | GTTTGGAAAGCACAG[A/T]CTATAAAAACATAGA | 6709 |
rs769115531 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582061 | TTGAAGACATAATAC[A/C]ACTTTATGGAAAAAT | 6709 |
rs769130912 | snp | A/G | 1.65302e-05 | 0.00287486 | missense | SPTAN1 | GRCh38.p7 | 9:128585778 | AGGATGTGAAGGCCA[A/G]GCTTCACGAGCTGAA | 6709 |
rs769200048 | snp | A/G | 5.09359e-05 | 0.00504632 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618145 | CTCCCGGGAACAAGT[A/G]GAAGGCCAGCACCCA | 6709 |
rs769232867 | snp | C/G | 1.66145e-05 | 0.00288218 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582437 | AGGCCAAGCTTGGGA[C/G]TAGTGTGCTTACCAA | 6709 |
rs769251271 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613820 | ACCACTCCGGCCAAC[A/G]TGGTGAGACCTCCGT | 6709 |
rs769263723 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627508 | GACCAGGTGCCAGCC[C/T]GCTGGGGCCGGGGAG | 6709 |
rs769272029 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625463 | AGTTCTCCTAAGCGA[A/G]ATCATGAGGGGTGAA | 6709 |
rs769281608 | snp | A/C | 3.29766e-05 | 0.00406045 | missense | SPTAN1 | GRCh38.p7 | 9:128576938 | TCTTTGGGGCAGCAG[A/C]AGTTCAGCGCTTTAA | 6709 |
rs769287410 | snp | C/T | 1.65018e-05 | 0.00287239 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632542 | GGCAGCAGGGCTGCC[C/T]GCTGAGCCGCCCTCG | 6709 |
rs769291812 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611525 | CATTTCCTTCCTCCT[C/T]TGCTAACTCCCCAAG | 6709 |
rs769308461 | snp | A/C | 1.64909e-05 | 0.00287144 | missense | SPTAN1 | GRCh38.p7 | 9:128609268 | ATGAGTCGTACAAGG[A/C]TCCCACCAACATCCA | 6709 |
rs769320860 | snp | A/G | 1.6473e-05 | 0.00286988 | missense | SPTAN1 | GRCh38.p7 | 9:128581848 | CTTCTTAAGAAGCAC[A/G]AAGACTTTGAGAAAT | 6709 |
rs769338215 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599282 | TGGAATTCCACGCAT[A/G]TGGCACCACACCCAG | 6709 |
rs769349794 | snp | A/T | 1.65116e-05 | 0.00287324 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605292 | CACCACTTTCTTCCC[A/T]TAGGTAAACTCCCTT | 6709 |
rs769356785 | snp | A/G | 1.64966e-05 | 0.00287194 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619015 | CCAGGTGAGACAGAA[A/G]CCAAAGGTGTCACCT | 6709 |
rs769380003 | in-del | -/TAAA | 0.000148249 | 0.00860829 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577300 | AAGCAGCTGATTCTG[-/TAAA]TAAGTTACCAAGGGT | 6709 |
rs769380398 | snp | A/C | 1.65348e-05 | 0.00287526 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128584459 | TTGCAGCAGCTCTTC[A/C]GGGATGTTGAGGATG | 6709 |
rs769416159 | in-del | -/AT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587364 | GCTGGGATTACAGGC[-/AT]ATAAGCCTCTGTGCC | 6709 |
rs769425571 | snp | C/T | 1.66065e-05 | 0.00288149 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621144 | ATAGTGTGCCTTGGC[C/T]GCTTCTACTCCAGGG | 6709 |
rs769426014 | snp | C/T | 1.65622e-05 | 0.00287764 | synonymous-codon, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633229 | GACCCGGGAACAAGC[C/T]GACTACTGCGTCTCC | 6709 |
rs769468805 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562291 | TATTTTTAGTAGAGA[G/T]GTGGTTTCACCATGT | 6709 |
rs769471750 | in-del | -/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581640 | AAGGACTTTAGACTT[-/C]CTAGAAGAGATCTTA | 6709 |
rs769488004 | snp | C/T | 3.29908e-05 | 0.00406132 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128626432 | CAAAAAGGCTTCTGC[C/T]TTCAACAGCTGGTTT | 6709 |
rs769496710 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626795 | ACGAGCAGGATGGAG[A/G]AGCATGGTTTCATCA | 6709 |
rs769505700 | in-del | -/C | 0.000808607 | 0.020091 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630424 | CCCTTCACCCAGCCA[-/C]CCCCCAGGGTACCCC | 6709 |
rs769518627 | in-del | -/TATGTGCT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574973 | GCTGCTCTCTAGGTG[-/TATGTGCT]ATTCTGTAACTCTGA | 6709 |
rs769519842 | snp | C/G | 1.6623e-05 | 0.00288292 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583061 | GATAGAAAGAACCCC[C/G]TTCTTTTATTCACAG | 6709 |
rs769549817 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579585 | TCAGCACCTTGTTTT[C/T]ATTTTGTAAGATGCT | 6709 |
rs769575186 | snp | A/T | 1.67826e-05 | 0.00289673 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575389 | ACAACATTATTATGT[A/T]AACTTTTTAGTATAT | 6709 |
rs769577034 | in-del | -/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619600 | GTGTGTCTATTCACA[-/T]TTCTGTGTTCTGTTG | 6709 |
rs769628464 | in-del | -/TC | 0.000808601 | 0.020091 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617628 | CTGTGCTGTTTCCCA[-/TC]TCTCATTCAGGGAGA | 6709 |
rs769642034 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563823 | TAATTTTTTTTTTAG[A/G]GCCAGGGTTTAGCCA | 6709 |
rs769659893 | snp | A/G | 1.64789e-05 | 0.0028704 | missense | SPTAN1 | GRCh38.p7 | 9:128568894 | TGCATCTGAAACCAT[A/G]CGGGTGAGTATGAGT | 6709 |
rs769663978 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605838 | CTCTACCAAAAGTAC[A/C]AAAATTAGCCAGGTG | 6709 |
rs769668578 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128578137 | CCTTGCTGACTTCCG[C/T]GACCTCACCAGCTGG | 6709 |
rs769690020 | snp | A/G | 1.6912e-05 | 0.00290787 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588958 | GGCAAGGCACAGAGA[A/G]TGGCTGTGTGTTTGT | 6709 |
rs769726464 | snp | G/T | 1.64754e-05 | 0.00287009 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600128 | AAGGTAAGAACTCCT[G/T]TGCAAATTATTGTTT | 6709 |
rs769732902 | in-del | -/TT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586114 | CATTTTTCACTTGGT[-/TT]TTTTTTTTTTTTTTT | 6709 |
rs769733032 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128609140 | GCGACGTCTGAAAGC[C/T]CAGATGATTGAGAAA | 6709 |
rs769772229 | snp | A/C | 1.65258e-05 | 0.00287448 | missense, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633288 | GCCGCGAGCTCCCCA[A/C]CGCGTTCGACTACGT | 6709 |
rs769801752 | snp | A/G | 1.65471e-05 | 0.00287633 | missense | SPTAN1 | GRCh38.p7 | 9:128585765 | CATTTTGCTGCAGAG[A/G]ATGTGAAGGCCAAGC | 6709 |
rs769831605 | snp | C/T | 1.65056e-05 | 0.00287272 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632495 | TTTAAGTGAGTTCAG[C/T]CTTACTCGCCCTGGC | 6709 |
rs769854111 | snp | A/G | 1.64735e-05 | 0.00286993 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627984 | GGCTTGTCATGTGGG[A/G]GTCTCGTGCGCTTGC | 6709 |
rs769855749 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599116 | TTTTGTGTGTAAAGA[C/T]TTGTGGAAAACTCCA | 6709 |
rs769857503 | snp | C/T | 1.64893e-05 | 0.0028713 | missense | SPTAN1 | GRCh38.p7 | 9:128574678 | TGAAACTTTCAGACC[C/T]GTTTGATGGAGCTGC | 6709 |
rs769859369 | snp | C/T | 4.94222e-05 | 0.00497078 | missense | SPTAN1 | GRCh38.p7 | 9:128630341 | GTATGGTGGAAGAGT[C/T]GGGGACCCTCGAATC | 6709 |
rs769949608 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629553 | CCCCACCAAGGCCAC[A/G]CGCACCGTGTGATTC | 6709 |
rs769952674 | snp | A/T | | | missense | SPTAN1 | GRCh38.p7 | 9:128566771 | GTCAAAGTGCTGGAA[A/T]CAGCAGAGGACATCC | 6709 |
rs769980005 | snp | A/G | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554380 | TATGTCACAGGCTGC[A/G]GTGTAAGCCTGTCAA | 6709 |
rs769985964 | in-del | -/AG | | | downstream-variant-500B, intron-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128634022 | AGTAAGAGAAACTCT[-/AG]AGACCAACCACATGG | 6709 |
rs769996442 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128555529 | TGCCTGCATGACGTT[C/T]CTGTTAAACAAATTG | 6709 |
rs770015410 | snp | C/G | 1.6483e-05 | 0.00287076 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599040 | AAGGACTTAAATCTT[C/G]GGAAGAATATCAAGC | 6709 |
rs770046688 | snp | A/G | 0.000413705 | 0.0143764 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582853 | GAAGCTTATAAAGTA[A/G]TGTACTGTTAGTGTT | 6709 |
rs770066601 | snp | A/G | 0.000100376 | 0.00708365 | downstream-variant-500B, missense | SPTAN1, WDR34 | GRCh38.p7 | 9:128633805 | CGGGGCCCTTGTTCC[A/G]TGAACTCTGTGCTCA | 6709 |
rs770086897 | snp | A/G | 1.64727e-05 | 0.00286986 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627882 | TGCTGCTGTTGTCCG[A/G]ACACCACCTTGTCTC | 6709 |
rs770101520 | snp | A/G | 3.29527e-05 | 0.00405898 | missense | SPTAN1 | GRCh38.p7 | 9:128607955 | CCAGCCCTGAGATCA[A/G]GCAGAAACTTGATAT | 6709 |
rs770116373 | snp | C/T | 8.79871e-05 | 0.00663218 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630143 | AACGGGAGAAATGCT[C/T]CCTGCCATCCCTCGA | 6709 |
rs770133448 | snp | A/G | 3.29897e-05 | 0.00406125 | missense | SPTAN1 | GRCh38.p7 | 9:128618032 | GATGACAACACCATC[A/G]GGAAAGAGGAGATCC | 6709 |
rs770141127 | in-del | -/CTT | 1.66237e-05 | 0.00288298 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583061 | GATAGAAAGAACCCC[-/CTT]CTTTTATTCACAGGA | 6709 |
rs770171975 | snp | C/T | 1.64885e-05 | 0.00287123 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128605160 | CTTCGAGAGGGACCT[C/T]GCGGCTCTCGGTGAC | 6709 |
rs770187977 | in-del | -/ATA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606485 | GACATATATATATAT[-/ATA]TTTTTTTTTTGGGGG | 6709 |
rs770189298 | snp | C/T | 4.94482e-05 | 0.00497209 | missense | SPTAN1 | GRCh38.p7 | 9:128607858 | TTTTGGCAGGAACAC[C/T]GGACAGAAATCGATG | 6709 |
rs770204355 | snp | G/T | 1.8253e-05 | 0.00302096 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628177 | GTCCTTGCCTCACTG[G/T]GCGATTCCAAGGGCT | 6709 |
rs770224141 | snp | A/G | 4.94605e-05 | 0.0049727 | missense | SPTAN1 | GRCh38.p7 | 9:128581007 | AGTGCATGGACCTGC[A/G]GCTCTTCTACCGGGA | 6709 |
rs770228127 | snp | C/T | 1.65067e-05 | 0.00287282 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583993 | AACTGGGGGCTGTGG[C/T]TGGGCAAGTGAATGC | 6709 |
rs770257194 | snp | A/G | 6.64529e-05 | 0.00576386 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591668 | GCTAGGCGTCCCATA[A/G]GCATACTCTGTTCCA | 6709 |
rs770295290 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560965 | ATGTTGCTGTGAACC[C/G]AGATAGCATCACTGC | 6709 |
rs770295291 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559591 | TTTCTTTACAAGAAA[A/G]TTTTGGAAGCAAACA | 6709 |
rs770301872 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565921 | TTCCTGACATTTTTA[A/G]TCACTTTAGGAAATT | 6709 |
rs770303060 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574650 | CAGTTGTGATCTGAT[C/T]AAAACTCTGATTTGA | 6709 |
rs770311257 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625552 | CTGGGGCGGGAGAGC[A/G]GAAGGCTGGGGTCAG | 6709 |
rs770314406 | snp | C/T | 1.64825e-05 | 0.00287071 | missense | SPTAN1 | GRCh38.p7 | 9:128583845 | GCAATGTTGAGGATA[C/T]TGAATTGTGGCTATA | 6709 |
rs770329771 | snp | A/C | 3.30011e-05 | 0.00406195 | missense | SPTAN1 | GRCh38.p7 | 9:128575296 | CAGATATGGCTGCTC[A/C]TGAAGAAAGAGTTAA | 6709 |
rs770356488 | snp | C/T | 1.64874e-05 | 0.00287113 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617954 | GCACCAGAAGAGCTA[C/T]CTGCTGTTAACCTCC | 6709 |
rs770358940 | snp | A/G | 4.95103e-05 | 0.00497521 | missense | SPTAN1 | GRCh38.p7 | 9:128632693 | CCTGAGTTCGAGGCA[A/G]TCCTGGACACGGTGG | 6709 |
rs770359554 | snp | A/C/T | 3.30536e-05 | 0.00406521 | missense | SPTAN1 | GRCh38.p7 | 9:128584370 | AGAAGAAACAGGAAG[A/C/T]CCTCGTGGCTCGCTA | 6709 |
rs770378486 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581152 | TTGTTTTAGGACATC[A/T]GTACCATGTTAGTTC | 6709 |
rs770385653 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587431 | TGATTGTCCCAAAAG[A/G]TGAGAATCCTGAAAA | 6709 |
rs770391198 | snp | A/G | 3.30071e-05 | 0.00406232 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605021 | TCTTAACCTGAATGT[A/G]TCTCGCCTTTAGAGA | 6709 |
rs770393431 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589898 | GGTTCTTACTCCAGA[C/G]TACAAGCTACATCTC | 6709 |
rs770419563 | snp | C/T | 1.72338e-05 | 0.00293541 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618155 | CAAGTGGAAGGCCAG[C/T]ACCCAAGGGCAGACT | 6709 |
rs770447296 | snp | A/C | 1.65927e-05 | 0.00288029 | missense | SPTAN1 | GRCh38.p7 | 9:128588926 | GATATCCTTACCTTA[A/C]TCAACAGCACCAACA | 6709 |
rs770483554 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633508 | CAGTCACAATCATCA[G/T]GTCACTGTGGGGACC | 6709 |
rs770505302 | snp | A/G | 1.67343e-05 | 0.00289255 | downstream-variant-500B, synonymous-codon | SPTAN1, WDR34 | GRCh38.p7 | 9:128633840 | CCACACCTTCACTGT[A/G]CCCTGGGCATCGCCC | 6709 |
rs770511577 | snp | A/G | 1.65203e-05 | 0.002874 | missense | SPTAN1 | GRCh38.p7 | 9:128626391 | CTCTTCTGCTTCCAG[A/G]TGGAGGACCTCTTCC | 6709 |
rs770532796 | snp | A/T | 6.58935e-05 | 0.00573955 | missense | SPTAN1 | GRCh38.p7 | 9:128630322 | CCTTCCACGTTTAGG[A/T]CCTGTATGGTGGAAG | 6709 |
rs770533632 | snp | A/T | 3.29495e-05 | 0.00405877 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609117 | TCATGGTTTCACTCT[A/T]TCAGGTGGCGACGTC | 6709 |
rs770557345 | in-del | -/TC | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598946 | ATAATAAAACTGGTT[-/TC]TCTCTCTCCTTGTAG | 6709 |
rs770562548 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572972 | CTTTCTCCTTTCAAG[G/T]AAAACATCCACACTT | 6709 |
rs770631178 | in-del | -/TTTA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622738 | TGACTTGTAGTATGG[-/TTTA]TTTATTTATTTATTT | 6709 |
rs770634123 | snp | C/T | 3.29739e-05 | 0.00406028 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607834 | CCAGTTACCTAATCC[C/T]TTCCCTCCTTTTGGC | 6709 |
rs770641858 | snp | C/T | 1.64874e-05 | 0.00287113 | missense | SPTAN1 | GRCh38.p7 | 9:128585834 | AAAGCTTCCCAGCGT[C/T]GGCAGGACCTGGAGG | 6709 |
rs770656741 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559995 | CCGCCTTGGCCTCCC[A/G]AAGTGCTGGGATTAC | 6709 |
rs770663882 | snp | A/G | 2.49554e-05 | 0.00353229 | missense, intron-variant | SPTAN1 | GRCh38.p7 | 9:128593005 | ATAACTAAGGAGGCC[A/G]GCAGTGTATCTCTGC | 6709 |
rs770665518 | snp | A/T | 1.65124e-05 | 0.00287331 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605274 | CCTTACTGCAAGCTC[A/T]TTCACCACTTTCTTC | 6709 |
rs770681406 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591341 | AAAGTGCTGGGATTA[C/T]AGGTGTGAGCCACTG | 6709 |
rs770681890 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604671 | GCGTGGTGGCTCATG[C/T]CTGTAATCCCAGCAC | 6709 |
rs770707043 | snp | A/G | 3.31945e-05 | 0.00407383 | missense | SPTAN1 | GRCh38.p7 | 9:128624346 | AATCACCATGAGGAG[A/G]ACATCTCTTCAAAGA | 6709 |
rs770719996 | in-del | -/AGAAAA | 1.64732e-05 | 0.0028699 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618851 | TATGGCTGATTTTCT[-/AGAAAA]TCCTGTCTCCTGTAA | 6709 |
rs770771886 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605730 | GGCACAGTGGCTCAC[A/G]TCTATAACCCCAGCA | 6709 |
rs770772851 | snp | G/T | 3.30972e-05 | 0.00406786 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568731 | CAAAATGCTGATGCT[G/T]TGTGGTTGCGTCTGA | 6709 |
rs770777758 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573868 | CAAGTGATTCTCCTG[C/T]CTCAGCCTTCTGAGT | 6709 |
rs770796388 | snp | G/T | 1.70374e-05 | 0.00291863 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577538 | AGGTCTTAACCAGTA[G/T]CATTTGGCTTCTTTT | 6709 |
rs770796456 | snp | C/T | 1.64963e-05 | 0.00287192 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128582810 | GCTCAAGAGTTGGGT[C/T]AATGAGAAGATGAAA | 6709 |
rs770834334 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629463 | CCTGGGGAGATTGCA[C/G]AGCTAACCCTGGCTC | 6709 |
rs770884419 | in-del | -/G | 1.64743e-05 | 0.00287 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608087 | ACCAAGTGTTTCCTT[-/G]CTGAAGGGCCTCATT | 6709 |
rs770897817 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606307 | TTTGAACCTGGAGGC[A/G]GAGGTTGCAGTGAGC | 6709 |
rs770908801 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581078 | ATCTGTGAGCAAAGC[C/G]TTGCCAGTGGTGGGA | 6709 |
rs770928578 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128591581 | GGAGAATCTCCTGGA[A/G]GAGCAAGGCAGCATA | 6709 |
rs770946272 | snp | A/T | 1.64792e-05 | 0.00287042 | missense | SPTAN1 | GRCh38.p7 | 9:128575260 | TAGAGGTTTTACAGA[A/T]GAAATTTGAAGAGTT | 6709 |
rs770948927 | in-del | -/TC | 0.00154873 | 0.0277843 | intron-variant, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633194 | AGGCACCAGGTGCCA[-/TC]TCTTACCCCACAGAA | 6709 |
rs770983670 | snp | C/T | 3.31181e-05 | 0.00406914 | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633377 | CTGCTTGCCCTGCGT[C/T]GCCTTGCTGCATGTC | 6709 |
rs771003904 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622224 | CACACCCAGACAACA[C/T]TCTCTGTTCTTCAAG | 6709 |
rs771009235 | snp | C/T | | | missense | SPTAN1 | GRCh38.p7 | 9:128574693 | CGTTTGATGGAGCTG[C/T]ACCGCCAGTGGGAAT | 6709 |
rs771011759 | snp | C/T | 1.65198e-05 | 0.00287395 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605008 | TGTACTTGGCATTTC[C/T]TAACCTGAATGTGTC | 6709 |
rs771016112 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568713 | CACGGGGAACAGCGG[G/T]GACAAAATGCTGATG | 6709 |
rs771019045 | in-del | -/G | 1.66676e-05 | 0.00288679 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632362 | GCTCAGCCCAGAGCA[-/G]GGGGGAGGAAAAGAC | 6709 |
rs771122318 | snp | A/G | 1.6473e-05 | 0.00286988 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584703 | GTTGGATAACTGGGG[A/G]CTGGTGTCTGCTTTC | 6709 |
rs771123623 | snp | A/G | | | downstream-variant-500B, intron-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128634008 | AGACAGATACGTGGA[A/G]TAAGAGAAACTCTAG | 6709 |
rs771159949 | snp | C/T | 3.29554e-05 | 0.00405914 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584852 | GAGGAAGGTGAGTGA[C/T]TGGTATCAGTGACAT | 6709 |
rs771165521 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585248 | TGGTCAGGCTGGTCT[G/T]GAACTCCTGACCTCA | 6709 |
rs771194437 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566182 | CTGCCTTAGCCTCCT[C/G]AGTAGCTGGTACCAT | 6709 |
rs771249131 | snp | A/C | 1.66032e-05 | 0.0028812 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566689 | CTAATTACTTTTCAT[A/C]TATTTTGGTGCCTAT | 6709 |
rs771251003 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558781 | GTGGAAGGAATGTGG[C/G]ACGCCCAGGCCGAGC | 6709 |
rs771256002 | snp | A/G | 1.73357e-05 | 0.00294407 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583288 | AACTGAAAGGTAAGA[A/G]ATGTTCCATTGAATT | 6709 |
rs771262997 | snp | C/G/T | 4.96909e-05 | 0.00498432 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632871 | CGAAACTGAGAACGT[C/G/T]AAGTCCAGCGAGGAG | 6709 |
rs771266011 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588706 | CTCATGAGTGTATAT[G/T]TGGTACATTTGGTAC | 6709 |
rs771268974 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558701 | GTTCTCTGTGAAGTC[A/G]GCCTTATCAGTCTGC | 6709 |
rs771282535 | snp | A/T | 1.65059e-05 | 0.00287275 | missense | SPTAN1 | GRCh38.p7 | 9:128566832 | ACCACCGCTTCAAGG[A/T]ACTCTCAACCCTTAG | 6709 |
rs771286283 | snp | A/G | 1.64768e-05 | 0.00287021 | missense | SPTAN1 | GRCh38.p7 | 9:128625859 | CTCGCCGCCAAACAC[A/G]TTCAGTCCAAGGCCA | 6709 |
rs771294979 | snp | A/G | 1.79686e-05 | 0.00299733 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628089 | CCTTCTCGTCACCTG[A/G]TGAGGAGTGTGTGCC | 6709 |
rs771356826 | snp | A/G | 1.65021e-05 | 0.00287241 | missense | SPTAN1 | GRCh38.p7 | 9:128587676 | GCATCCAGGCTTTGC[A/G]AGAACAAGCACAGTC | 6709 |
rs771370468 | in-del | -/AAAG | 1.64933e-05 | 0.00287165 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574853 | TGCTAAGCTTTACTC[-/AAAG]AAAAGGGAAGAGACT | 6709 |
rs771373881 | snp | A/C | 3.51253e-05 | 0.00419063 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628164 | GCCAGGGGGAGCCGT[A/C]CTTGCCTCACTGGGC | 6709 |
rs771387723 | in-del | -/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606008 | AAAAAAAAAAAAAAA[-/T]TAAAAACAGAAAAAA | 6709 |
rs771404039 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615140 | ACAAACTGTCAGTAT[G/T]CTTTGAAGTGACAGG | 6709 |
rs771417146 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581552 | GAAGCAACAAAAACT[A/G]TGTAAGAGAAGTTTC | 6709 |
rs771431868 | in-del | -/AGAG | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128555210 | GCTATACAGAATGTC[-/AGAG]AGAAGACACTGAAAA | 6709 |
rs771450682 | snp | C/T | 5.1873e-05 | 0.00509253 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576791 | GAGCCAGAAGTTGTG[C/T]ACAAATCCAGTCTCT | 6709 |
rs771456936 | snp | C/T | 3.2994e-05 | 0.00406152 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632632 | CAAATCTTGCCTGCG[C/T]TCCCTGGGCTATGAC | 6709 |
rs771460214 | snp | A/G | 1.64991e-05 | 0.00287215 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580911 | CTGACCATGTCTCCT[A/G]TGCCCCCAAGCTGAC | 6709 |
rs771464146 | snp | A/G | 1.69347e-05 | 0.00290982 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632981 | CAGGAGGTGGGTGAA[A/G]AGGTGTCCTTTGGAA | 6709 |
rs771469654 | snp | C/T | 1.65529e-05 | 0.00287683 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608317 | GAGTCTGGATTTTTC[C/T]TGATTGACATCTGTT | 6709 |
rs771489152 | snp | C/T | 1.65671e-05 | 0.00287807 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625757 | CAAATTGGCTTGTCA[C/T]TCCTTGTTCAGGAAA | 6709 |
rs771512726 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633571 | CCGACTTCAGAAAAT[A/C]GAAGCAGCTGGCTCC | 6709 |
rs771555109 | snp | A/G | 1.64876e-05 | 0.00287116 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128583819 | AGCCAACCAGCAACA[A/G]CAATTTAATCGCAAT | 6709 |
rs771562394 | snp | A/G | 3.37041e-05 | 0.00410498 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567022 | AAATTCAAGAGCCCA[A/G]ATGTTCTTACCCAAA | 6709 |
rs771572025 | in-del | -/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621283 | CATTGGTAAGACCTC[-/G]CATCGCCCACTGGGA | 6709 |
rs771580135 | snp | C/G | 1.64743e-05 | 0.00287 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599010 | CGGGTGCTGTGTGTG[C/G]ATCTTGAACATGAGA | 6709 |
rs771588342 | snp | A/G | 6.59957e-05 | 0.005744 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605026 | ACCTGAATGTGTCTC[A/G]CCTTTAGAGATGCTG | 6709 |
rs771593254 | snp | C/G/T | 0.000162206 | 0.00900426 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628182 | TGCCTCACTGGGCGA[C/G/T]TCCAAGGGCTCACTT | 6709 |
rs771600903 | snp | A/G | 1.65979e-05 | 0.00288074 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584018 | GAATGCAGAAACTAT[A/G]GGAGGGAGGAAAAGC | 6709 |
rs771618221 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631865 | TCCTGGAGTCCTCGC[C/T]GTACTTGTCCTTGGC | 6709 |
rs771631539 | snp | A/G | 1.6483e-05 | 0.00287076 | missense | SPTAN1 | GRCh38.p7 | 9:128568832 | AACTCAGGAGCCATT[A/G]TTAAGCTGGATGAAA | 6709 |
rs771636267 | snp | A/G | 1.68035e-05 | 0.00289853 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587713 | GGTAAACTTGTAACA[A/G]TTTATGGGTTACTGG | 6709 |
rs771649957 | snp | A/G | 0.000173653 | 0.00931646 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630157 | TCCCTGCCATCCCTC[A/G]ATCCCTGGGGCCCAT | 6709 |
rs771651648 | snp | C/T | 3.31526e-05 | 0.00407127 | missense | SPTAN1 | GRCh38.p7 | 9:128625973 | GCTCAGAGTCACTTC[C/T]GCAAGGTGAGGATGG | 6709 |
rs771654389 | snp | C/G | 1.69481e-05 | 0.00291098 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577525 | CAAATAATGCTCCAG[C/G]TCTTAACCAGTATCA | 6709 |
rs771675198 | snp | C/T | 1.66322e-05 | 0.00288371 | missense | SPTAN1 | GRCh38.p7 | 9:128632902 | ATTGAGAGCGCCTTC[C/T]GGGCCCTCAGCTCAG | 6709 |
rs771695175 | snp | A/G | 1.64735e-05 | 0.00286993 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630302 | CAGGCCCCTTTCCTC[A/G]CTGTCCTTCCACGTT | 6709 |
rs771695666 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622735 | ATGTGACTTGTAGTA[C/T]GGTTTATTTATTTAT | 6709 |
rs771700745 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578749 | CAGGAGAATCGCTTG[A/G]ACCCGGGAGGCAGAG | 6709 |
rs771729069 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581262 | TCAGAAAAGGCCCCA[C/G]CTTTTCAGATTAGTG | 6709 |
rs771736269 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616997 | AATCCCAACACTTTG[A/G]GAGACCGAGGTGGGC | 6709 |
rs771746797 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620605 | CACCTGTAATCCCAG[C/G]TACTTGGGAGGCTGA | 6709 |
rs771776226 | snp | A/G | 1.65745e-05 | 0.00287871 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588784 | ACGTGTTTTTACCAT[A/G]TTTGCCCTTCCTTTG | 6709 |
rs771798239 | snp | C/T | 3.2975e-05 | 0.00406035 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608986 | TGGACAGGTGGGTGT[C/T]CTGTGGCACTGACAT | 6709 |
rs771825373 | snp | C/T | 3.30136e-05 | 0.00406273 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632428 | TTTCTGTTTTTCTTC[C/T]AGGAACACAACAGGT | 6709 |
rs771827974 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600026 | CTGGAAAGGCCAGGT[G/T]CTTTGTTTCATGGTC | 6709 |
rs771828238 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603206 | TTTTTTTTCCGGAAT[G/T]TTCTCCTGTAGTATA | 6709 |
rs771838658 | snp | A/C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597776 | CTGCCTCAACCTCCC[A/C/G]AACAGCTGGGATTAC | 6709 |
rs771856455 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572187 | TTTTCCAACCTGTAC[G/T]TCATTCCTGTCTTCT | 6709 |
rs771862017 | snp | C/T | 6.62405e-05 | 0.00575464 | missense | SPTAN1 | GRCh38.p7 | 9:128605476 | TTCCTTAGCGATTTC[C/T]GGTACGGAGCCATGT | 6709 |
rs771886198 | snp | A/G | 0.000148298 | 0.00860971 | missense | SPTAN1 | GRCh38.p7 | 9:128615728 | AGGGACACCATCAAC[A/G]GGCGCTTCCAGAAGA | 6709 |
rs771890978 | snp | C/G | 1.64991e-05 | 0.00287215 | missense | SPTAN1 | GRCh38.p7 | 9:128577418 | AGTGCAACACAGATT[C/G]AAGTGAAGCGAGAGG | 6709 |
rs771898438 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572771 | ACTTTCACACCATAC[C/T]GGACAGCGTGGCGCC | 6709 |
rs771900336 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558988 | CTGTCAGGTTAAGAG[A/G]GGGGAAACTCTCACT | 6709 |
rs771906889 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | SPTAN1 | GRCh38.p7 | 9:128575205 | CCTGAATAGGAAGCA[A/G]TTGTTACTTCTGAAG | 6709 |
rs771921943 | snp | A/G | 1.66346e-05 | 0.00288393 | missense | SPTAN1 | GRCh38.p7 | 9:128621213 | CCGTCCACAAGGATC[A/G]CGTGAATGATGTCTG | 6709 |
rs771925044 | snp | A/G | 1.64765e-05 | 0.00287019 | missense | SPTAN1 | GRCh38.p7 | 9:128584840 | AATGCCATGGTGGAG[A/G]AAGGTGAGTGATTGG | 6709 |
rs771927052 | snp | A/G | 3.29565e-05 | 0.00405921 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582594 | CTCCTCCTTTTTGGT[A/G]CATGAATGTCTCTTC | 6709 |
rs771948130 | in-del | -/AA/AAA/AAAA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561015 | GCAAGACCCCATCTC[-/AA/AAA/AAAA]AAAAAAAAAAAAAAA | 6709 |
rs771968361 | snp | A/G | 3.05535e-05 | 0.00390843 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598525 | TGTCTCCATCTTGGA[A/G]TGAGGCTCTGTTGCT | 6709 |
rs771973581 | snp | C/G | 1.66308e-05 | 0.00288359 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624313 | GACCAGTGTGTGCCT[C/G]TCTCCATGGCCTAGA | 6709 |
rs771987118 | in-del | -/TTTCT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629107 | GGTGTATTCATTTGG[-/TTTCT]TTTCTTTGAATAGCA | 6709 |
rs772001965 | snp | C/T | 0.000296741 | 0.0121771 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607820 | GTGGGCATCTGCTGC[C/T]AGTTACCTAATCCCT | 6709 |
rs772014766 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584689 | CTTTTCTCTTCATGG[C/T]TGGATAACTGGGGAC | 6709 |
rs772060922 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603619 | ACCAGCTCCTCTGAT[C/T]TCCCCTGGTTTTCTC | 6709 |
rs772065617 | in-del | -/AGAG | 1.68472e-05 | 0.0029023 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588953 | AACAAGGCAAGGCAC[-/AGAG]AGTGGCTGTGTGTTT | 6709 |
rs772073109 | snp | A/C | 1.67203e-05 | 0.00289134 | missense | SPTAN1 | GRCh38.p7 | 9:128583242 | ATGAATGAGGTGATC[A/C]GTTTGTGGAAGAAAC | 6709 |
rs772119238 | snp | A/G | 3.29495e-05 | 0.00405877 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128582726 | TGCCCTTCACGAGAG[A/G]GCCATGCGTCGCCGG | 6709 |
rs772123932 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631745 | GGCAGGAGAATCACT[A/T]GAACCCGGGAGGTTG | 6709 |
rs772148883 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128601894 | GGGCCAGGCATGGGT[A/G]TACACCTTTCCTTCT | 6709 |
rs772158389 | in-del | -/T | 0.00162118 | 0.0284247 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627188 | AGGTCCGCCTCTTCC[-/T]TTGAAGCCCCTGGGG | 6709 |
rs772211512 | in-del | -/C | 7.81616e-05 | 0.00625098 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632118 | CATCTGTGCTCCCCA[-/C]CCCTGCAGCGCAAGC | 6709 |
rs772272532 | snp | G/T | 1.65949e-05 | 0.00288048 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625725 | GAAGAGCAAGTTCCA[G/T]TCCTGTGGAGTCACC | 6709 |
rs772281075 | snp | C/T | 1.64887e-05 | 0.00287125 | missense | SPTAN1 | GRCh38.p7 | 9:128580973 | GAGCTGTGGGAGCTG[C/T]GCAGGCAGCAGTACG | 6709 |
rs772281155 | snp | A/G | 1.64961e-05 | 0.00287189 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574857 | AAGCTTTACTCAAAG[A/G]AAAGGGAAGAGACTC | 6709 |
rs772283250 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617397 | GTGATGCCTCCCATC[C/T]TCCAGTGCATCCCCA | 6709 |
rs772294529 | snp | A/T | 1.65872e-05 | 0.00287981 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609298 | AGGTAAGCTGAAGTG[A/T]CTGGGTGTTGGTCTT | 6709 |
rs772344436 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621345 | AAAGTTCACTTCCTG[A/G]GATGTTCACCAAACC | 6709 |
rs772367229 | snp | A/G | 3.29734e-05 | 0.00406025 | missense | SPTAN1 | GRCh38.p7 | 9:128576947 | CAGCAGAAGTTCAGC[A/G]CTTTAACAGGTGTCA | 6709 |
rs772382171 | snp | C/T | 3.30147e-05 | 0.00406279 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128617715 | CCTGAGGAAGAAGCA[C/T]AAGCGGCTGGAAGCA | 6709 |
rs772399471 | snp | C/T | 1.6968e-05 | 0.00291268 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628071 | CTGCACTTCCCCTCC[C/T]ACCCTTCTCGTCACC | 6709 |
rs772409000 | snp | A/C/G | 4.94942e-05 | 0.00497444 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128611897 | ATGACCACCGTCACT[A/C/G]TCAACCTGATATAAT | 6709 |
rs772419280 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569358 | CTGTTAAAGCTCCAG[C/G]TCTAAGGAATGATGT | 6709 |
rs772423453 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128556169 | GAGGTTGCAATGAGC[C/T]GAGATTGCACCATTG | 6709 |
rs772423730 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579294 | GGCCAGGGAGGGACT[C/T]GCCCTACCAGGTTCT | 6709 |
rs772435490 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128577132 | TTTGTTCTGTAGGGA[C/T]GTGGATGAGACTATC | 6709 |
rs772442030 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557181 | AGTCCCTAAAAATCC[A/C]TTTCTTGCAAAACTG | 6709 |
rs772463904 | snp | C/T | 1.64963e-05 | 0.00287192 | missense | SPTAN1 | GRCh38.p7 | 9:128632630 | TTCAAATCTTGCCTG[C/T]GCTCCCTGGGCTATG | 6709 |
rs772488907 | snp | C/T | 1.6517e-05 | 0.00287372 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632734 | GTAAATTAATTAAGG[C/T]CAGGTGCTGTGAGCC | 6709 |
rs772513871 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600703 | AGTATTGCCCTGTCA[C/T]CCAGGCTGGAGTGCA | 6709 |
rs772516765 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630488 | TGCTATTATTGTACC[C/G]TTTTCCCTTGGCCTA | 6709 |
rs772530985 | snp | A/G | 1.67097e-05 | 0.00289043 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581942 | CCTTATAGTAAGCCA[A/G]AGTCTTTTTCCCTGG | 6709 |
rs772533230 | snp | C/G | 6.58892e-05 | 0.00573936 | missense | SPTAN1 | GRCh38.p7 | 9:128608136 | CCTCTTTAGCTGTTC[C/G]ATCGGGACTGTGAGC | 6709 |
rs772554445 | in-del | -/AG | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614757 | GCACTCTTGGATGAC[-/AG]AGCAAGGAAAAAAAA | 6709 |
rs772557668 | snp | A/G | 1.70589e-05 | 0.00292047 | downstream-variant-500B, synonymous-codon | SPTAN1, WDR34 | GRCh38.p7 | 9:128633932 | GGGTTTGCTTGATCA[A/G]AACTGTGGGTTTCTG | 6709 |
rs772560297 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569932 | AATAATTATTAACTA[C/T]TACTAATAATGATGA | 6709 |
rs772575290 | snp | G/T | 1.65364e-05 | 0.0028754 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594138 | TACAGCTAACTGCCT[G/T]CCTTGTCCCTCTTGT | 6709 |
rs772576047 | snp | A/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128626620 | TCCGCGTAGCCTCCA[A/G]CCCCTACACCTGGTT | 6709 |
rs772608327 | snp | A/C | 1.65471e-05 | 0.00287633 | missense | SPTAN1 | GRCh38.p7 | 9:128583126 | ATCAGGCTTTTGAGG[A/C]TGAGCTCTCAGCAAA | 6709 |
rs772615544 | snp | A/G | 1.64735e-05 | 0.00286993 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568725 | CGGGGACAAAATGCT[A/G]ATGCTGTGTGGTTGC | 6709 |
rs772615772 | snp | C/T | 8.26617e-05 | 0.00642838 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628184 | CCTCACTGGGCGATT[C/T]CAAGGGCTCACTTTG | 6709 |
rs772660788 | snp | A/G | 1.69516e-05 | 0.00291127 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613528 | GAGTGCCTGGGACAC[A/G]GCTCTGCCTGACTCC | 6709 |
rs772665724 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631566 | TGCAGTGGCTCATGC[C/T]TATAATCCCAGAACT | 6709 |
rs772694787 | snp | A/G | 1.65696e-05 | 0.00287828 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588788 | GTTTTTACCATGTTT[A/G]CCCTTCCTTTGGATT | 6709 |
rs772707499 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632959 | GAGCTCTACCAGGTA[C/T]GGGCCTCAGGAGGTG | 6709 |
rs772708633 | snp | C/T | 5.19422e-05 | 0.00509592 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630161 | TGCCATCCCTCGATC[C/T]CTGGGGCCCATTAGG | 6709 |
rs772724247 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572772 | CTTTCACACCATACC[A/G]GACAGCGTGGCGCCC | 6709 |
rs772728946 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633664 | TGACTTCCCCCAAAG[C/T]TTTGCTTTTCTTCAT | 6709 |
rs772771772 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128594283 | ACAGCAATGGATCAA[C/T]GAGAAGGAAGCCGCT | 6709 |
rs772780483 | snp | C/G/T | 8.30922e-05 | 0.00644516 | missense | SPTAN1 | GRCh38.p7 | 9:128624419 | CAGCCCAGAGAAAGG[C/G/T]GAAGCTGGATGAGAA | 6709 |
rs772834217 | in-del | -/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610359 | AGGAACAGAAGAAGA[-/G]GGTAATGGGACTTTT | 6709 |
rs772861283 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592418 | TAGCTGGGACTGCTG[A/G]CACATGCCACCATGC | 6709 |
rs772861546 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622807 | GCCCAGGCTGGAGTG[C/T]ACTGGCGCAATCTCA | 6709 |
rs772874810 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590297 | CCAGTAGAACTTTCT[G/T]TGATGGTGGAAATGT | 6709 |
rs772875751 | snp | A/G | 1.69438e-05 | 0.00291061 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632982 | AGGAGGTGGGTGAAG[A/G]GGTGTCCTTTGGAAA | 6709 |
rs772894632 | snp | C/T | 0.000339357 | 0.0130216 | downstream-variant-500B, synonymous-codon | SPTAN1, WDR34 | GRCh38.p7 | 9:128633750 | CGGGACCCCTCAGGC[C/T]GCCACCTCTGCTGCC | 6709 |
rs772902568 | snp | C/T | 1.66632e-05 | 0.0028864 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625991 | AAGGTGAGGATGGGG[C/T]CACGTGAAGCTTAGC | 6709 |
rs772912310 | in-del | -/AAAC | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569537 | GAAGATATTAAGGGA[-/AAAC]AAACCTCTTGACAGT | 6709 |
rs772937581 | snp | A/G | 1.64912e-05 | 0.00287147 | missense | SPTAN1 | GRCh38.p7 | 9:128605177 | CGGCTCTCGGTGACA[A/G]GGTGAGAGGACCCAA | 6709 |
rs772942037 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617147 | CGGAGGCTGAGGTGG[A/G]AGGATCACTTGAACC | 6709 |
rs772942960 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604493 | CCCCCAAGCTTGCTG[A/G]CTGAGATCCTAGAGC | 6709 |
rs772957209 | snp | A/G | 1.65993e-05 | 0.00288086 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584019 | AATGCAGAAACTATA[A/G]GAGGGAGGAAAAGCC | 6709 |
rs772963154 | in-del | -/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621605 | ACCCATAAAGCCCCA[-/C]CCTGACACCACACAT | 6709 |
rs772985392 | snp | C/T | 1.69657e-05 | 0.00291248 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577529 | TAATGCTCCAGGTCT[C/T]AACCAGTATCATTTG | 6709 |
rs772994758 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620713 | ATAGAGCAAGAACTC[C/T]GTCTCAAAAAGAAAA | 6709 |
rs772995493 | snp | A/G | 3.32707e-05 | 0.00407851 | missense | SPTAN1 | GRCh38.p7 | 9:128632903 | TTGAGAGCGCCTTCC[A/G]GGCCCTCAGCTCAGA | 6709 |
rs773019990 | snp | C/T | 1.64749e-05 | 0.00287005 | missense | SPTAN1 | GRCh38.p7 | 9:128582739 | AGAGCCATGCGTCGC[C/T]GGGCCCAGCTAGCCG | 6709 |
rs773023641 | snp | C/T | 8.24899e-05 | 0.00642169 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605027 | CCTGAATGTGTCTCG[C/T]CTTTAGAGATGCTGA | 6709 |
rs773027341 | snp | A/G | 1.64866e-05 | 0.00287106 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608989 | ACAGGTGGGTGTCCT[A/G]TGGCACTGACATAGT | 6709 |
rs773036348 | snp | A/G | 1.6623e-05 | 0.00288292 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624322 | GTGCCTCTCTCCATG[A/G]CCTAGAACAATCACC | 6709 |
rs773037255 | snp | A/G | 0.000587371 | 0.0171272 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626972 | AGCACGTGCCACCAC[A/G]CCTGGCTAATTATTT | 6709 |
rs773065786 | snp | A/G | 1.68599e-05 | 0.00290338 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587717 | AACTTGTAACAGTTT[A/G]TGGGTTACTGGAGGG | 6709 |
rs773097197 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628570 | TGTCCCGCCCAGTCC[C/T]GGCAGGGACTTCTCT | 6709 |
rs773099952 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571629 | AAAAAACCTATTAAA[C/T]ATAGTTTGTTGAGTA | 6709 |
rs773113715 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631752 | GAATCACTTGAACCC[A/G]GGAGGTTGCAGTGAG | 6709 |
rs773114282 | snp | A/G | 8.96499e-05 | 0.00669454 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609620 | CCACATCAGTGTACT[A/G]AACTCTTGTTCTTTT | 6709 |
rs773128134 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564954 | ATAATACCAGGCAGG[C/G]ATGTTGGGCCAGATT | 6709 |
rs773140619 | snp | A/G | 5.30556e-05 | 0.00515024 | missense | SPTAN1 | GRCh38.p7 | 9:128604365 | CTACAGCAGCTGGCC[A/G]AGGAACGGAGCCAGC | 6709 |
rs773153524 | snp | A/G | 3.40594e-05 | 0.00412656 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598535 | TTGGAGTGAGGCTCT[A/G]TTGCTGTAAGGATGC | 6709 |
rs773214983 | in-del | -/G | 0.000272517 | 0.0116698 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627200 | TTCCTTGAAGCCCCT[-/G]GGGGGTGGGAACAGA | 6709 |
rs773260096 | snp | A/G | 7.03589e-05 | 0.00593081 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628119 | CTTGCCCCATAGCCC[A/G]TGGTCCCTGGTCCCC | 6709 |
rs773270953 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128553114 | CCCGGTCCCTTCCCT[C/T]GGCCGGGAGCGACTT | 6709 |
rs773275366 | in-del | -/AG | 0.5 | 0 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588953 | AACAAGGCAAGGCAC[-/AG]AGAGTGGCTGTGTGT | 6709 |
rs773288283 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563806 | ATGCCACCATGCCTG[A/G]ATAATTTTTTTTTTA | 6709 |
rs773288631 | snp | A/G | 3.29533e-05 | 0.00405901 | missense | SPTAN1 | GRCh38.p7 | 9:128574727 | TTTTGGAGAAGATGC[A/G]AGAAAAAGGAATCAA | 6709 |
rs773306747 | snp | C/T | 1.68196e-05 | 0.00289992 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609311 | TGACTGGGTGTTGGT[C/T]TTGATGTAGCCTTAT | 6709 |
rs773328719 | snp | G/T | 3.29489e-05 | 0.00405874 | missense | SPTAN1 | GRCh38.p7 | 9:128582727 | GCCCTTCACGAGAGA[G/T]CCATGCGTCGCCGGG | 6709 |
rs773332005 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595373 | CCTCAGCTTCCCAAG[A/G]TGCTGGGATTACAGG | 6709 |
rs773333330 | snp | A/G | 1.64732e-05 | 0.0028699 | missense | SPTAN1 | GRCh38.p7 | 9:128591571 | CAGCCTCCCGGGAGA[A/G]TCTCCTGGAGGAGCA | 6709 |
rs773334557 | in-del | -/AA | 1.64765e-05 | 0.00287019 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607733 | TGCTGAGTAGCAAAG[-/AA]ACGTGGCTGCTCTGC | 6709 |
rs773345967 | snp | C/T | | | intron-variant, synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128629167 | CTATCAGTATGAAGT[C/T]GGGGATGATCTGTCT | 6709 |
rs773365387 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128553896 | TTAAGTAAAACAGAA[-/TG]TATCAAAGATGGAAG | 6709 |
rs773418092 | in-del | -/CA | 1.66757e-05 | 0.00288749 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632350 | GCTGTGGGCCAGGCT[-/CA]CAGCCCAGAGCAGGG | 6709 |
rs773435271 | snp | A/G | 6.60491e-05 | 0.00574632 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128585947 | CACTGACTATGGCAA[A/G]GACGAAGACTCTGCT | 6709 |
rs773459701 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128577150 | GGATGAGACTATCAG[C/T]TGGATTAAGGAAAAG | 6709 |
rs773461609 | snp | A/G | 1.65154e-05 | 0.00287358 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617604 | AAAGCAGGGAGGTGC[A/G]GAGACTGACTGTGCT | 6709 |
rs773465512 | snp | C/G | 1.65946e-05 | 0.00288046 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625730 | GCAAGTTCCAGTCCT[C/G]TGGAGTCACCACAAA | 6709 |
rs773466651 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621369 | CCAAACCAAGGTCTG[C/T]GTGGAGACCAGCAGC | 6709 |
rs773474201 | snp | A/G | 1.64977e-05 | 0.00287203 | missense | SPTAN1 | GRCh38.p7 | 9:128632631 | TCAAATCTTGCCTGC[A/G]CTCCCTGGGCTATGA | 6709 |
rs773485341 | snp | A/C/G | 9.89714e-05 | 0.00703398 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574859 | GCTTTACTCAAAGAA[A/C/G]AGGGAAGAGACTCCT | 6709 |
rs773492406 | snp | A/G | 8.24151e-05 | 0.00641878 | missense | SPTAN1 | GRCh38.p7 | 9:128618995 | GGCGACACTCTTGCC[A/G]CCATCCAGGTGAGAC | 6709 |
rs773501997 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581423 | GGCTGCAGCAAGCTA[A/T]GATCGTACCACCGCA | 6709 |
rs773503642 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128555938 | TTAAAAAATAGCTCT[C/T]GGGCTGGGTGCGGTG | 6709 |
rs773529609 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613813 | GTTCGAGACCACTCC[A/G]GCCAACGTGGTGAGA | 6709 |
rs773558073 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606123 | ACGCCTGTAATCCCA[A/G]CACTTTGGGAAGTCA | 6709 |
rs773621155 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600712 | CTGTCACCCAGGCTG[A/G]AGTGCAGTGGCACAA | 6709 |
rs773628261 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579296 | CCAGGGAGGGACTCG[C/T]CCTACCAGGTTCTAT | 6709 |
rs773639656 | in-del | -/A | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571841 | CTTTGTCCAGTCACC[-/A]CTATTTGTTTTATTT | 6709 |
rs773657969 | snp | A/G | 0.000162167 | 0.00900316 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128555354 | CCCTCTTTAGACTCC[A/G]CATTCCTCCATCATG | 6709 |
rs773663318 | snp | A/G | 4.95062e-05 | 0.004975 | missense | SPTAN1 | GRCh38.p7 | 9:128579662 | ATGCCCATGAAGACA[A/G]CTTCAAATCTGCAGA | 6709 |
rs773684837 | in-del | -/G | 3.43755e-05 | 0.00414567 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586011 | CAGGGAAGTGGAACA[-/G]GGCTTGTACTGAGAA | 6709 |
rs773754706 | snp | C/T | 6.95096e-05 | 0.00589491 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628080 | CCCTCCCACCCTTCT[C/T]GTCACCTGATGAGGA | 6709 |
rs773759802 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587113 | GGCGTGAGGCACCGC[A/G]CTCGTTCTGTCGCTA | 6709 |
rs773764220 | snp | C/T | 1.65288e-05 | 0.00287474 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632773 | GGGCACCCACCTGCC[C/T]TCCCTGCTCAGGCTC | 6709 |
rs773794297 | snp | A/G | 4.32779e-05 | 0.00465157 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628112 | TGTGTGCCTTGCCCC[A/G]TAGCCCATGGTCCCT | 6709 |
rs773801018 | snp | G/T | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554438 | GAGAGCTGTTTTAAG[G/T]ATGTCTTTTGGTTCC | 6709 |
rs773841175 | snp | C/T | 2.02472e-05 | 0.0031817 | missense | SPTAN1 | GRCh38.p7 | 9:128598473 | AGTCTGAAGGTCTCA[C/T]GGCAGAGGAGGTGCA | 6709 |
rs773841663 | snp | C/G | 1.64811e-05 | 0.00287059 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625093 | ATATTTTCCACACTT[C/G]GTTTTCTAGGTGAAA | 6709 |
rs773854405 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578862 | AAAAAAAACCTTCTG[A/G]GAGGTTTTAATGTGC | 6709 |
rs773861549 | snp | A/G | 1.65987e-05 | 0.00288082 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566699 | TTCATCTATTTTGGT[A/G]CCTATTGGTACTTAT | 6709 |
rs773878824 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557410 | TGCCAGGTTTACAGA[A/G]TCCAGAGCATTTGAC | 6709 |
rs773917839 | in-del | -/AG | 1.69115e-05 | 0.00290782 | downstream-variant-500B, frameshift-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128633903 | CTCCAGACAGTAGAC[-/AG]GGCTTTCATCCTGGG | 6709 |
rs773992218 | snp | C/T | 7.57949e-05 | 0.00615562 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628179 | CCTTGCCTCACTGGG[C/T]GATTCCAAGGGCTCA | 6709 |
rs774026314 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602111 | CACCTTCTGACTCCT[A/G]TAAACACACGGGTTG | 6709 |
rs774045397 | snp | C/T | 6.58892e-05 | 0.00573936 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128612219 | CTTCAACACAGGGAT[C/T]AAGGACTTTGACTTC | 6709 |
rs774051017 | snp | A/T | 1.65111e-05 | 0.0028732 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128566851 | CTCAACCCTTAGGCG[A/T]CAGAAGCTGGAAGAT | 6709 |
rs774056435 | snp | A/G | 1.65798e-05 | 0.00287917 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608827 | GGCAGTCCAGGCAGG[A/G]CCCAGCCACAGGCCC | 6709 |
rs774059444 | in-del | -/TT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589577 | CGCCGTGCCCGGCCT[-/TT]TTTTTTTTTTTTTTT | 6709 |
rs774089510 | snp | A/G | 1.65078e-05 | 0.00287291 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128594343 | GGAGCAGGTTGAGGT[A/G]CTCCAGAAGAAGTTT | 6709 |
rs774094821 | snp | A/G | 1.66868e-05 | 0.00288845 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587707 | CTGCCGGGTAAACTT[A/G]TAACAGTTTATGGGT | 6709 |
rs774100497 | snp | A/T | 1.64811e-05 | 0.00287059 | missense | SPTAN1 | GRCh38.p7 | 9:128583860 | TTGAATTGTGGCTAT[A/T]TGAAGTAGAAGGTCA | 6709 |
rs774108521 | snp | A/C | 6.61157e-05 | 0.00574922 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609287 | CACCAACATCCAGGT[A/C]AGCTGAAGTGACTGG | 6709 |
rs774115997 | snp | G/T | 3.29554e-05 | 0.00405914 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582589 | TCATGCTCCTCCTTT[G/T]TGGTACATGAATGTC | 6709 |
rs774135440 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570179 | TAGAATATGTAACCA[C/G]CTTACAGATGGGGAA | 6709 |
rs774146471 | snp | C/G | 1.66258e-05 | 0.00288316 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626725 | GAGCTGCTCGGCCTC[C/G]CAGAGCCCTCTCTGG | 6709 |
rs774153565 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571456 | CAAGCGTGGTGTTGC[A/G]TGCCTGTAATCCCAG | 6709 |
rs774156565 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587730 | TTATGGGTTACTGGA[G/T]GGAGGCCTTGAAGGA | 6709 |
rs774198117 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128609158 | GATGATTGAGAAAAG[A/G]TCAAAGCTAGGAGAA | 6709 |
rs774198198 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569376 | TAAGGAATGATGTGT[A/G]GCACCTATTGGTCAA | 6709 |
rs774209726 | snp | G/T | 0.000313188 | 0.0125098 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574836 | TTTTGGGAAGAAGGG[G/T]TTGCTAAGCTTTACT | 6709 |
rs774215534 | snp | C/T | 0.000157894 | 0.0088838 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632115 | GAGCATCTGTGCTCC[C/T]CACCCCTGCAGCGCA | 6709 |
rs774249310 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563897 | CCCACCTCAGCCTCC[C/G]AAAGTGCTGGGATTG | 6709 |
rs774252764 | snp | A/G | 4.94588e-05 | 0.00497262 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625057 | TTTCCTTTCTAATCC[A/G]TCTCCACTGAGGAGG | 6709 |
rs774280374 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607493 | TCAGTAGATCAGATT[A/T]ACCCAAGATAACTTT | 6709 |
rs774283264 | snp | A/G | 1.65282e-05 | 0.00287469 | missense | SPTAN1 | GRCh38.p7 | 9:128584490 | AGGAGACGTGGATTC[A/G]AGAGAAAGAGCCCAT | 6709 |
rs774303070 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128577234 | TCTGCTTCGGAAGCA[C/T]GAGGGTCTGGAGAGA | 6709 |
rs774323431 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592045 | TGTCCTCTTTCCTCT[A/G]GCTGAGCCCCCATAT | 6709 |
rs774367720 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627292 | GGGGAGGTTCCTTGT[C/G]GGGAGGCCACCACCA | 6709 |
rs774379865 | snp | A/G | 1.65334e-05 | 0.00287514 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128584389 | CGTGGCTCGCTATGA[A/G]GCACTCAAGGAGCCC | 6709 |
rs774384865 | in-del | -/C | 0.000413158 | 0.0143669 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578268 | TATCTCTAGAATCTT[-/C]CAGAAGTGAAGATTT | 6709 |
rs774394963 | snp | A/G | 1.6522e-05 | 0.00287414 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582465 | CAATGAAGAACTCTT[A/G]TCTTCCTTCCTAGGC | 6709 |
rs774397953 | snp | A/G | 3.29603e-05 | 0.00405944 | missense | SPTAN1 | GRCh38.p7 | 9:128574697 | TGATGGAGCTGCACC[A/G]CCAGTGGGAATTACT | 6709 |
rs774410639 | snp | A/G | 1.65688e-05 | 0.00287821 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128583091 | GGATCCATCCAACCT[A/G]CAAGGAAAAGTACAG | 6709 |
rs774447298 | snp | G/T | 1.65184e-05 | 0.00287384 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617600 | CTTGAAAGCAGGGAG[G/T]TGCAGAGACTGACTG | 6709 |
rs774451164 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587067 | CTCAAGTGATCTGCC[G/T]GCCTCAGCCTCGCAA | 6709 |
rs774470705 | snp | A/G | 3.29533e-05 | 0.00405901 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600147 | AAATTATTGTTTTCA[A/G]GAGTTTTGCGAGATC | 6709 |
rs774472270 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603611 | AAGCAGTGACCAGCT[C/T]CTCTGATCTCCCCTG | 6709 |
rs774488815 | in-del | -/CT | 0.000190812 | 0.00976575 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626733 | CGGCCTCCCAGAGCC[-/CT]CTCTGGGCCCTGCTC | 6709 |
rs774527953 | snp | A/G | 1.64836e-05 | 0.0028708 | missense | SPTAN1 | GRCh38.p7 | 9:128611786 | ATCCGTGGGGTTATC[A/G]ACATGGGCAACTCCC | 6709 |
rs774532821 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630445 | AGGGTACCCCTTCCC[G/T]TCCTGGCTTAAAGTC | 6709 |
rs774541647 | snp | G/T | 1.66635e-05 | 0.00288643 | missense | SPTAN1 | GRCh38.p7 | 9:128624443 | ATGAGAACTCGGCCT[G/T]CCTTCAGTTCAACTG | 6709 |
rs774559979 | snp | C/T | 1.64762e-05 | 0.00287016 | missense | SPTAN1 | GRCh38.p7 | 9:128607984 | ATTCTTGACCAGGAG[C/T]GTGCAGACCTGGAGA | 6709 |
rs774604729 | snp | C/T | 1.6752e-05 | 0.00289408 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579613 | GCTGGGCACAAATCA[C/T]GGCTTTGTTTTTTTC | 6709 |
rs774607395 | snp | A/C | 1.6708e-05 | 0.00289028 | downstream-variant-500B, synonymous-codon | SPTAN1, WDR34 | GRCh38.p7 | 9:128633828 | TGTGCTCAGCTGCCA[A/C]ACCTTCACTGTGCCC | 6709 |
rs774610766 | snp | A/G | 1.65343e-05 | 0.00287521 | missense, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633248 | TACTGCGTCTCCCAC[A/G]TGAAGCCCTACGTGG | 6709 |
rs774611049 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128556036 | ACCAGCCTGGCCAAC[A/G]TAGTGAAACCCCATC | 6709 |
rs774618446 | snp | C/T | 1.64735e-05 | 0.00286993 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627997 | GGGGTCTCGTGCGCT[C/T]GCCCCTCGTGGCCTG | 6709 |
rs774629616 | in-del | -/TT | 1.64943e-05 | 0.00287174 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612084 | CATAGATTTCATCTC[-/TT]TTTGGCTCCCTTCTG | 6709 |
rs774632692 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561389 | AAAAAAAAGGCCAGG[C/T]GCGGTGGCTCACGCC | 6709 |
rs774649396 | snp | A/G | 1.70067e-05 | 0.002916 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618148 | CCGGGAACAAGTGGA[A/G]GGCCAGCACCCAAGG | 6709 |
rs774657717 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568137 | AAAGAAAATTGTTTC[A/G]GTAGCAAGTGGAACA | 6709 |
rs774659049 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128591497 | GTGGAAAGTGGAAGT[A/G]AACGATCGTCAGGGT | 6709 |
rs774683959 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586042 | GGAAGTTAGGAGAAG[C/T]AGTGATGCGCGGGAG | 6709 |
rs774703790 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625501 | GGTCAGGGAGAGAGG[C/G]AGGGCGAGTGTTCTG | 6709 |
rs774737956 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577788 | CTGAGTATCACATGA[A/G]ATATCTTATTAAAAC | 6709 |
rs774745286 | snp | A/G | 6.80874e-05 | 0.0058343 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588968 | AGAGAGTGGCTGTGT[A/G]TTTGTTCCACGCTGG | 6709 |
rs774792328 | snp | A/T | 1.65619e-05 | 0.00287762 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582863 | AAGTAATGTACTGTT[A/T]GTGTTGCCATGTAGC | 6709 |
rs774839238 | in-del | -/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567282 | GAATGAGGTTTTTTG[-/T]TTTGTTTTGTTTTGT | 6709 |
rs774862492 | snp | A/G | 1.64887e-05 | 0.00287125 | missense | SPTAN1 | GRCh38.p7 | 9:128585921 | CGGGAGAAGGAACCC[A/G]TTGTGGGCAGCACTG | 6709 |
rs774930310 | snp | A/G | 1.6504e-05 | 0.00287258 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128605322 | TGGTGAAACAGCAGA[A/G]CGCCTGATCCAGTCC | 6709 |
rs774947865 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613919 | CTGAGGTAGGAGAAT[C/T]ACTTGAGCCCAGGAG | 6709 |
rs774982401 | snp | C/G | 1.64827e-05 | 0.00287073 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576968 | ACAGGTGTCAAGCCA[C/G]AGTGGGCTTTGGGGA | 6709 |
rs774982753 | snp | A/C | 1.66073e-05 | 0.00288156 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582439 | GCCAAGCTTGGGACT[A/C]GTGTGCTTACCAATG | 6709 |
rs774998332 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627895 | CGGACACCACCTTGT[C/T]TCCCGGCTGCTTGGA | 6709 |
rs774998542 | snp | C/G | 1.64961e-05 | 0.00287189 | missense | SPTAN1 | GRCh38.p7 | 9:128632622 | ATCAGGAGTTCAAAT[C/G]TTGCCTGCGCTCCCT | 6709 |
rs775028350 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569749 | CCCTTAAGCCCCAGC[C/T]AGAACTGTTTTGTCT | 6709 |
rs775031314 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612625 | TGGAAAGCACAGACT[A/G]TAAAAACATAGAGGT | 6709 |
rs775091220 | snp | C/T | 1.6525e-05 | 0.00287441 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632756 | CTGTGAGCCTCTGCC[C/T]GGGGCACCCACCTGC | 6709 |
rs775177064 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | SPTAN1 | GRCh38.p7 | 9:128577211 | CGAGACCTGGCAAGT[A/G]TTCAGGCTCTGCTTC | 6709 |
rs775177320 | snp | A/G | 1.66023e-05 | 0.00288113 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566691 | AATTACTTTTCATCT[A/G]TTTTGGTGCCTATTG | 6709 |
rs775190610 | snp | C/T | 3.46795e-05 | 0.00416396 | missense | SPTAN1 | GRCh38.p7 | 9:128626607 | CAGATCAAGAGCTTC[C/T]GCGTAGCCTCCAACC | 6709 |
rs775192555 | snp | A/G | 0.000725641 | 0.019034 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618845 | AGGAGATTATGGCTG[A/G]TTTTCTTCCTGTCTC | 6709 |
rs775213765 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563839 | GCCAGGGTTTAGCCA[C/T]ATTACCTAGGCTGTT | 6709 |
rs775217886 | snp | C/T | 5.10417e-05 | 0.00505156 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615874 | CTAGAAGGCCCCTTA[C/T]GCCTGTAATAGTGGG | 6709 |
rs775219507 | snp | A/G | 1.64874e-05 | 0.00287113 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609023 | CAGCCCTGAGAGGAT[A/G]CATCCCCTCATACGA | 6709 |
rs775224497 | snp | A/G | 6.58903e-05 | 0.00573941 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128612162 | GGTGCAAAAGTCAGC[A/G]GAAAAGAGCCAGAAA | 6709 |
rs775227647 | snp | C/G/T | 1.65985e-05 | 0.00288079 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587577 | GCTTCAGCCCCTGCA[C/G/T]AGTGCTCCATGTGTG | 6709 |
rs775240859 | snp | A/G | 1.64776e-05 | 0.00287028 | missense | SPTAN1 | GRCh38.p7 | 9:128594306 | AAGCCGCTCTGACAA[A/G]TGAGGAGGTCGGAGC | 6709 |
rs775245294 | snp | A/G | 3.30589e-05 | 0.00406551 | missense | SPTAN1 | GRCh38.p7 | 9:128584465 | CAGCTCTTCCGGGAT[A/G]TTGAGGATGAGGAGA | 6709 |
rs775274851 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581288 | TAGTGTGATGTAAAA[C/T]GTTTTATTAAAGAGA | 6709 |
rs775279108 | snp | C/T | 3.295e-05 | 0.00405881 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128594295 | CAATGAGAAGGAAGC[C/T]GCTCTGACAAGTGAG | 6709 |
rs775282851 | snp | A/G | 6.77469e-05 | 0.00581969 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632096 | GAGCTGAGGGCCCCC[A/G]TCTGAGCATCTGTGC | 6709 |
rs775305903 | snp | A/G | 1.64762e-05 | 0.00287016 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128615757 | GATCAAGAGCATGGC[A/G]GCCTCCCGGCGAGCC | 6709 |
rs775332792 | snp | C/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128625822 | AGGCATTGCCAACAT[C/G]ACTGCCCTCAAAGAT | 6709 |
rs775345372 | snp | G/T | 3.38221e-05 | 0.00411216 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588959 | GCAAGGCACAGAGAG[G/T]GGCTGTGTGTTTGTT | 6709 |
rs775368190 | snp | G/T | 5.10634e-05 | 0.00505263 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579589 | CACCTTGTTTTTATT[G/T]TGTAAGATGCTGGGC | 6709 |
rs775368425 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627887 | CTGTTGTCCGGACAC[C/T]ACCTTGTCTCCCGGC | 6709 |
rs775396061 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574039 | ATTACAGGCATGAGC[C/T]GCTGCACCCAGCCTC | 6709 |
rs775398517 | snp | C/T | 1.81404e-05 | 0.00301162 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624539 | AGAGCTGCTCTTTGT[C/T]TCCTTCCGTGTCATT | 6709 |
rs775408148 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562444 | TTGGGAGTGGGAGAG[A/G]AGAGTGCACTCCTGG | 6709 |
rs775473151 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592805 | TCTAATTTTCCTGCT[A/G]TTTCTTTACTGTCAT | 6709 |
rs775486293 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619937 | CGTGGCTGGGCTGAG[A/G]GATCCATCACACACT | 6709 |
rs775505553 | snp | C/T | 1.64955e-05 | 0.00287184 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128588838 | CACGGATGATGAGAC[C/T]GGGAAGGAGCTGGTC | 6709 |
rs775527593 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605853 | AAAAATTAGCCAGGT[C/G]TGGTGGCAGGCATCT | 6709 |
rs775533851 | snp | A/G | 1.64757e-05 | 0.00287012 | missense | SPTAN1 | GRCh38.p7 | 9:128578156 | CTCACCAGCTGGGTG[A/G]CTGAGATGAAAGCCC | 6709 |
rs775544430 | snp | A/G | 1.70035e-05 | 0.00291572 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128633003 | CCTTTGGAAAACTAA[A/G]GCCAAATTTGTGGCA | 6709 |
rs775545003 | snp | C/G | 1.65367e-05 | 0.00287543 | missense | SPTAN1 | GRCh38.p7 | 9:128585775 | CAGAGGATGTGAAGG[C/G]CAAGCTTCACGAGCT | 6709 |
rs775553506 | snp | A/G | 1.64792e-05 | 0.00287042 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630386 | CCAAAGTAAGTGCCC[A/G]TGGGGCTCTGGCCCA | 6709 |
rs775566979 | snp | C/T | 1.64887e-05 | 0.00287125 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128626477 | GGACTTAACAGACCC[C/T]GTGCGCTGCAACTCC | 6709 |
rs775574271 | snp | G/T | 1.65908e-05 | 0.00288012 | missense | SPTAN1 | GRCh38.p7 | 9:128624363 | CATCTCTTCAAAGAT[G/T]AAGGGCCTGAACGGG | 6709 |
rs775634580 | snp | A/G | 0.000296751 | 0.0121773 | missense | SPTAN1 | GRCh38.p7 | 9:128574679 | GAAACTTTCAGACCC[A/G]TTTGATGGAGCTGCA | 6709 |
rs775643068 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585538 | TTCTTAGAGTCTAGA[C/T]AGAGGTCATGGTTTG | 6709 |
rs775675004 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565928 | CATTTTTAGTCACTT[C/T]AGGAAATTGAGGCAT | 6709 |
rs775677327 | snp | C/T | 1.64863e-05 | 0.00287104 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617961 | AAGAGCTACCTGCTG[C/T]TAACCTCCTCGTCCT | 6709 |
rs775679777 | snp | C/G | 1.64798e-05 | 0.00287047 | missense | SPTAN1 | GRCh38.p7 | 9:128607890 | CAGGGCTGGCACTTT[C/G]CAGGCATTTGAGCAG | 6709 |
rs775697554 | snp | C/G | 1.65021e-05 | 0.00287241 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605023 | TTAACCTGAATGTGT[C/G]TCGCCTTTAGAGATG | 6709 |
rs775707176 | snp | A/G | 1.64928e-05 | 0.00287161 | missense | SPTAN1 | GRCh38.p7 | 9:128611762 | GAGCTGCATGCCAAC[A/G]CTGACCGGATCCGTG | 6709 |
rs775715661 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598009 | GCTGGAGTGCAATGG[C/T]GCAATCTCAGCTCAC | 6709 |
rs775754130 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628849 | CACCTGACTCCCCTC[C/T]CTGCCCCATGCCTGT | 6709 |
rs775771416 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609614 | GTGTGTCCACATCAG[G/T]GTACTGAACTCTTGT | 6709 |
rs775794646 | snp | A/G | 1.65353e-05 | 0.00287531 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128625957 | GAAGAAGCTTCTGGA[A/G]GCTCAGAGTCACTTC | 6709 |
rs775805555 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585161 | CTGGGACTACAGGGA[C/T]ACACCACCATACCCA | 6709 |
rs775811166 | snp | A/G | 1.64928e-05 | 0.00287161 | missense | SPTAN1 | GRCh38.p7 | 9:128591618 | CGGCAGGAGCAGATT[A/G]ACAATCAGTAAGGAT | 6709 |
rs775828981 | snp | A/G | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128553619 | ATATTTTAAATAAGC[A/G]CCTTGTTAAAAGTTG | 6709 |
rs775840579 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633550 | CTTGAAGCAGCTGCC[C/G]TCATTCCGACTTCAG | 6709 |
rs775877243 | snp | A/G | 1.94498e-05 | 0.00311841 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609698 | TTAAGAGTTGTAGTT[A/G]AATGAGCTCCAGTAT | 6709 |
rs775885056 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579562 | GGCTTATAATGCTTA[C/T]GTAAAATTCAGCACC | 6709 |
rs775886527 | snp | C/T | 3.29598e-05 | 0.00405941 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128625882 | CAAGGCCATCGAGGC[C/T]CGGCACGCCTCCCTC | 6709 |
rs775887133 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599342 | GTTTCACCATGTTGT[C/T]CAGGCTGGTCTCGAA | 6709 |
rs775919119 | snp | G/T | 2.83499e-05 | 0.00376486 | splice-acceptor-variant, intron-variant | SPTAN1 | GRCh38.p7 | 9:128592982 | TGCCCCCTCTGTGCA[G/T]GACACGCATAACTAA | 6709 |
rs775920857 | snp | A/G | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554409 | AAGCAATATGATGAA[A/G]AGGTGCACATGGGGA | 6709 |
rs775921579 | snp | A/G | 1.64901e-05 | 0.00287137 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584888 | GGTGCTGCTCCTCGT[A/G]TCTCCCCTTCTTGCC | 6709 |
rs775953883 | in-del | -/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588619 | CCAGACAAAATGAGA[-/T]TTTTTTTTTTAAAGA | 6709 |
rs775957658 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624007 | AGAATCTCTTGAACC[C/T]GGGAGGCGGAGGTTG | 6709 |
rs775974591 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623444 | ATATCATCTTAACTT[C/T]AAATTTCAGCCCATT | 6709 |
rs775991212 | snp | C/T | 1.85352e-05 | 0.00304421 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128604394 | GCTCTTGGGCAGCGC[C/T]CATGAAGTACAGAGG | 6709 |
rs776000538 | snp | A/G | 1.77565e-05 | 0.00297958 | downstream-variant-500B, utr-variant-3-prime | SPTAN1, WDR34 | GRCh38.p7 | 9:128633703 | CGTCAGAAACACAAG[A/G]CTCGGCACAGCGAAG | 6709 |
rs776000581 | snp | A/G | 1.64866e-05 | 0.00287106 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128581008 | GTGCATGGACCTGCA[A/G]CTCTTCTACCGGGAC | 6709 |
rs776004002 | snp | C/T | 3.29451e-05 | 0.00405851 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581735 | CACAGTCTTAGAAGA[C/T]CAAAGGAATAGGACA | 6709 |
rs776064912 | snp | C/T | 1.64781e-05 | 0.00287033 | missense | SPTAN1 | GRCh38.p7 | 9:128577364 | TAGGTCAAAGCCCTG[C/T]GTGCTGAGGCTGACC | 6709 |
rs776075636 | snp | A/G | 1.64866e-05 | 0.00287106 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609009 | ACTGACATAGTCACC[A/G]GCCCTGAGAGGATGC | 6709 |
rs776079416 | snp | A/G | 1.64977e-05 | 0.00287203 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128618037 | CAACACCATCGGGAA[A/G]GAGGAGATCCAGCAG | 6709 |
rs776108784 | snp | A/G | 1.74564e-05 | 0.0029543 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576772 | CCAGGGTAACTAGTT[A/G]GAGGAGCCAGAAGTT | 6709 |
rs776118703 | snp | A/G | 0.000179719 | 0.00947771 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626727 | GCTGCTCGGCCTCCC[A/G]GAGCCCTCTCTGGGC | 6709 |
rs776119131 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622720 | TTCTCTTTAAATTCA[A/G]TGTGACTTGTAGTAT | 6709 |
rs776141354 | in-del | -/G | 1.67826e-05 | 0.00289673 | downstream-variant-500B, frameshift-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128633866 | CGCCCGCAGCCAAGA[-/G]CTGAGTCTGCTGGCT | 6709 |
rs776156589 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567568 | TGCTGGGATTACAGG[C/T]GTGAGCCACCACACC | 6709 |
rs776169787 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579886 | GAGGTTTAAAAAGAA[G/T]GTATATGTATAGTGT | 6709 |
rs776197142 | snp | A/G | 5.14584e-05 | 0.00507214 | downstream-variant-500B, utr-variant-3-prime | SPTAN1, WDR34 | GRCh38.p7 | 9:128633736 | TTGCACCCGCCTCCC[A/G]GGACCCCTCAGGCCG | 6709 |
rs776213553 | in-del | -/G | | | downstream-variant-500B, frameshift-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128633790 | GGTCCTCAGCTTCCC[-/G]GGGGCCCTTGTTCCG | 6709 |
rs776239183 | snp | A/G | 1.70807e-05 | 0.00292234 | downstream-variant-500B, missense | SPTAN1, WDR34 | GRCh38.p7 | 9:128633937 | TGCTTGATCAAAACT[A/G]TGGGTTTCTGGGAGC | 6709 |
rs776244007 | in-del | -/AAGCACCAG | 1.66323e-05 | 0.00288373 | cds-indel | SPTAN1 | GRCh38.p7 | 9:128611717 | TGGTATTTTTAGAGC[-/AAGCACCAG]AAGCACCAGGCTTTT | 6709 |
rs776246263 | snp | C/T | 1.64947e-05 | 0.00287177 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605198 | GAGGACCCAAAGTCA[C/T]CTTCTGTCTGGCATT | 6709 |
rs776267211 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612787 | AAAAATTAGCCAGGC[C/G]TGGTGGCACGCTCCT | 6709 |
rs776279771 | snp | A/G | 1.65002e-05 | 0.00287225 | missense | SPTAN1 | GRCh38.p7 | 9:128585804 | CTGAACCAAAAGTGG[A/G]AGGCACTGAAAGCCA | 6709 |
rs776310053 | snp | C/T | 6.59359e-05 | 0.00574139 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576961 | CGCTTTAACAGGTGT[C/T]AAGCCAGAGTGGGCT | 6709 |
rs776318564 | snp | C/T | 1.65012e-05 | 0.00287234 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632554 | GCCTGCTGAGCCGCC[C/T]TCGGCTTTGTGCTGC | 6709 |
rs776327242 | snp | C/T | 0.00011738 | 0.00766003 | downstream-variant-500B, missense | SPTAN1, WDR34 | GRCh38.p7 | 9:128633851 | CTGTGCCCTGGGCAT[C/T]GCCCGCAGCCAAGAG | 6709 |
rs776353163 | snp | A/G | 1.64787e-05 | 0.00287038 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598930 | ATGTGTATTTCTTCT[A/G]ATAATAAAACTGGTT | 6709 |
rs776441600 | snp | C/T | 7.33936e-05 | 0.00605734 | synonymous-codon, intron-variant | SPTAN1 | GRCh38.p7 | 9:128593010 | TAAGGAGGCCGGCAG[C/T]GTATCTCTGCGTATG | 6709 |
rs776441728 | snp | C/T | 1.65121e-05 | 0.00287329 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605277 | TACTGCAAGCTCATT[C/T]ACCACTTTCTTCCCA | 6709 |
rs776448694 | snp | C/T | 1.65979e-05 | 0.00288074 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128624348 | TCACCATGAGGAGAA[C/T]ATCTCTTCAAAGATG | 6709 |
rs776449256 | snp | C/G | 1.64776e-05 | 0.00287028 | missense | SPTAN1 | GRCh38.p7 | 9:128615736 | CATCAACGGGCGCTT[C/G]CAGAAGATCAAGAGC | 6709 |
rs776473267 | snp | A/C/T | 1.6817e-05 | 0.0028997 | downstream-variant-500B, missense | SPTAN1, WDR34 | GRCh38.p7 | 9:128633874 | GCCAAGAGCTGAGTC[A/C/T]GCTGGCTGTTGAACT | 6709 |
rs776493422 | snp | A/T | 4.94254e-05 | 0.00497094 | missense | SPTAN1 | GRCh38.p7 | 9:128574757 | AACTGCTGCAGGCCC[A/T]GAAGTTGGTGCAGTA | 6709 |
rs776507647 | snp | A/T | 3.30049e-05 | 0.00406219 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632491 | GATGTTTAAGTGAGT[A/T]CAGCCTTACTCGCCC | 6709 |
rs776512074 | snp | A/G | 1.69622e-05 | 0.00291219 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632986 | GGTGGGTGAAGAGGT[A/G]TCCTTTGGAAAACTA | 6709 |
rs776529646 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618234 | GGCCTCACATGTGCC[A/G]TAGTCGGTTTGCTCC | 6709 |
rs776538429 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607821 | TGGGCATCTGCTGCC[A/G]GTTACCTAATCCCTT | 6709 |
rs776576977 | snp | C/T | 1.65173e-05 | 0.00287374 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128588820 | TTAGCAACAAGTGGC[C/T]CCCACGGATGATGAG | 6709 |
rs776597765 | snp | C/T | 1.72024e-05 | 0.00293273 | downstream-variant-500B, utr-variant-3-prime | SPTAN1, WDR34 | GRCh38.p7 | 9:128633734 | GCTTGCACCCGCCTC[C/T]CGGGACCCCTCAGGC | 6709 |
rs776612890 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629499 | GTTTTAAAAGGGTAG[A/G]TTGGGGTGAATGTGG | 6709 |
rs776623472 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604677 | TGGCTCATGCCTGTA[A/T]TCCCAGCACTTTGGG | 6709 |
rs776625840 | snp | G/T | 0.000229358 | 0.0107064 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627024 | TGCTATGTTGCCCAG[G/T]CTGGTCTTCAACTCC | 6709 |
rs776641301 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128573049 | TTTTCATTTTGCTAG[A/G]AGTGACATCTCAATC | 6709 |
rs776647691 | snp | C/G | 1.65078e-05 | 0.00287291 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128608927 | GCTCATCGCTGCCGG[C/G]CATTATGCCAAGGGA | 6709 |
rs776648566 | snp | A/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128605372 | ACCTGCAGGAAAAGT[A/G]CACAGAGTTAAACCA | 6709 |
rs776675967 | snp | A/G | 1.64779e-05 | 0.00287031 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128568882 | AGAAGGGCATTTTGC[A/G]TCTGAAACCATACGG | 6709 |
rs776677188 | snp | C/T | 1.65866e-05 | 0.00287976 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591662 | GCAAGGGCTAGGCGT[C/T]CCATAGGCATACTCT | 6709 |
rs776692287 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617377 | GGCTCCTCAGGGCAG[C/T]ACTAGTGATGCCTCC | 6709 |
rs776704955 | snp | C/G | 1.65954e-05 | 0.00288053 | missense, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633218 | CCACAGAACCTGACC[C/G]GGGAACAAGCCGACT | 6709 |
rs776714593 | in-del | -/AA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600263 | CTTTCTGAATCTGTT[-/AA]CTCTAAAATGTGATG | 6709 |
rs776725656 | in-del | -/AC | 1.73528e-05 | 0.00294552 | downstream-variant-500B, utr-variant-3-prime | SPTAN1, WDR34 | GRCh38.p7 | 9:128633696 | TGGCTTGCGTCAGAA[-/AC]ACAAGGCTCGGCACA | 6709 |
rs776728710 | snp | C/T | 1.64735e-05 | 0.00286993 | missense | SPTAN1 | GRCh38.p7 | 9:128607690 | GAGCTGAGGCATTGC[C/T]GGAGCGACACCAGGT | 6709 |
rs776729506 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579596 | TTTTTATTTTGTAAG[A/T]TGCTGGGCACAAATC | 6709 |
rs776740448 | snp | C/T | | | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128583856 | GATATTGAATTGTGG[C/T]TATATGAAGTAGAAG | 6709 |
rs776747224 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610879 | CCAATGTCTGTAGTA[C/G]CTGTAGATTTCTCCT | 6709 |
rs776765827 | snp | C/G | 1.65449e-05 | 0.00287614 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568736 | TGCTGATGCTGTGTG[C/G]TTGCGTCTGAGGCTC | 6709 |
rs776782747 | snp | A/C | 1.64876e-05 | 0.00287116 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128575282 | TGAAGAGTTTCAAAC[A/C]GATATGGCTGCTCAT | 6709 |
rs776789116 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606408 | CAAGTCTCTACTTTC[C/T]TATCCAAGTATGGGC | 6709 |
rs776794393 | snp | C/T | 4.95782e-05 | 0.00497862 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128625777 | TGTTCAGGAAACTTT[C/T]GACGCTGGGCTGCAG | 6709 |
rs776795375 | snp | C/T | 5.00981e-05 | 0.00500465 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632338 | GGTACCCGGGAGGGC[C/T]GTGGGCCAGGCTCAG | 6709 |
rs776816439 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621394 | AGCAGCAATTCCATT[C/T]CTGTGTTTCGTGACA | 6709 |
rs776820062 | snp | A/G | 0.000103386 | 0.00718904 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128627403 | GAGGGAGCTGGAGCT[A/G]CAGAAGGAACAGCGG | 6709 |
rs776859484 | snp | A/G | 1.65414e-05 | 0.00287583 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568741 | ATGCTGTGTGGTTGC[A/G]TCTGAGGCTCACTTC | 6709 |
rs776878433 | snp | A/G | 4.95193e-05 | 0.00497566 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128566833 | CCACCGCTTCAAGGA[A/G]CTCTCAACCCTTAGG | 6709 |
rs776914977 | snp | C/G | 0.00013777 | 0.00829854 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628174 | GCCGTCCTTGCCTCA[C/G]TGGGCGATTCCAAGG | 6709 |
rs776918499 | snp | C/T | | | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128550759 | ATTTTGTACCCAGAG[C/T]TGAATATCTGATCAA | 6709 |
rs776918984 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128560503 | CTCCAGCCCCAGCCT[C/T]CTGAGTAGATGGGAC | 6709 |
rs776926300 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600802 | CAAGTAGCTGGGACT[A/G]CAGGCATGTGCCACC | 6709 |
rs776927572 | snp | C/T | 1.64874e-05 | 0.00287113 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128613389 | TTGCCAGGTGGAGGC[C/T]CTGCTGGCATCCGAA | 6709 |
rs776933801 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602069 | ACCTTTATAAATCCC[A/G]GTACCTCTTATTGGA | 6709 |
rs776955235 | snp | C/G | 1.64808e-05 | 0.00287057 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582645 | TCTTCAACTGGATAT[C/G]CCTTTGGGAGTGAAC | 6709 |
rs776960254 | snp | C/T | 3.29468e-05 | 0.00405861 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575148 | GTTTCTGGAAGCCAT[C/T]GTTAACAAATGTTGG | 6709 |
rs776983295 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578373 | GTTTCTCATCATGAG[G/T]ATTATGGTTGGTTTT | 6709 |
rs776993477 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565899 | GAGACTTGAGAGCAC[G/T]TCGTTTTTCCTGACA | 6709 |
rs776999454 | snp | A/G | 1.65089e-05 | 0.00287301 | missense | SPTAN1 | GRCh38.p7 | 9:128611744 | CACCAGGCTTTTGAA[A/G]CAGAGCTGCATGCCA | 6709 |
rs777023504 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128588751 | GAATCTGCTCTGTAC[G/T]TAGATGACTCAGCGC | 6709 |
rs777029919 | in-del | -/CTT/CTTT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128555619 | GAAAATTTGCAAAGC[-/CTT/CTTT]CTTTTTTTTTTTTTT | 6709 |
rs777042103 | in-del | -/AA | 1.66327e-05 | 0.00288376 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632371 | CAGAGCAGGGGGAGG[-/AA]AAGACACAGTCACCT | 6709 |
rs777050169 | snp | C/G | 3.29968e-05 | 0.00406169 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580917 | ATGTCTCCTATGCCC[C/G]CAAGCTGACCGTCCT | 6709 |
rs777061288 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622376 | GTGATCTGGGCTCAC[C/T]GCAACCTCCACCTCC | 6709 |
rs777089739 | snp | C/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128632634 | AATCTTGCCTGCGCT[C/G]CCTGGGCTATGACCT | 6709 |
rs777110211 | snp | G/T | 3.29451e-05 | 0.00405851 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128608177 | CTGGATGGCTGCCCG[G/T]GAGGCCTTCTTGAAT | 6709 |
rs777123766 | snp | A/G | 1.72003e-05 | 0.00293255 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624511 | TGTCAGCAAGGCCCG[A/G]AAGAGCCTTCCCAGA | 6709 |
rs777143536 | snp | A/G | 1.78274e-05 | 0.00298553 | missense | SPTAN1 | GRCh38.p7 | 9:128604372 | AGCTGGCCGAGGAAC[A/G]GAGCCAGCTCTTGGG | 6709 |
rs777153325 | snp | A/G | 1.64871e-05 | 0.00287111 | missense | SPTAN1 | GRCh38.p7 | 9:128580988 | CGCAGGCAGCAGTAC[A/G]AGCAGTGCATGGACC | 6709 |
rs777182182 | snp | A/G | 1.64773e-05 | 0.00287026 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128625870 | ACACGTTCAGTCCAA[A/G]GCCATCGAGGCCCGG | 6709 |
rs777193357 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605709 | TTTAAAAATCAAAAA[C/T]GGCCAGGCACAGTGG | 6709 |
rs777249849 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562044 | GGTGGGTGGTCAGGG[A/T]GTGGAGACTTCTGAT | 6709 |
rs777267488 | snp | C/G | 3.30715e-05 | 0.00406628 | missense | SPTAN1 | GRCh38.p7 | 9:128617737 | CTGGAAGCAGAACTG[C/G]CTGCGCATGAGCCGG | 6709 |
rs777299280 | snp | A/T | 1.64887e-05 | 0.00287125 | missense | SPTAN1 | GRCh38.p7 | 9:128615822 | TCCGGGACATGGATG[A/T]CGAGGAGTCCTGGAT | 6709 |
rs777312802 | snp | C/G | 1.64776e-05 | 0.00287028 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128615730 | GGACACCATCAACGG[C/G]CGCTTCCAGAAGATC | 6709 |
rs777328879 | snp | A/G | 1.64868e-05 | 0.00287109 | missense | SPTAN1 | GRCh38.p7 | 9:128583830 | AACAGCAATTTAATC[A/G]CAATGTTGAGGATAT | 6709 |
rs777352630 | snp | C/T | 6.58946e-05 | 0.0057396 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591430 | CTCCTTGGATTCTCC[C/T]TCTCAGAGAAGGAAT | 6709 |
rs777355476 | snp | A/C | 1.66239e-05 | 0.00288299 | intron-variant, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633206 | CCATCTCTTACCCCA[A/C]AGAACCTGACCCGGG | 6709 |
rs777361183 | snp | C/T | 1.64749e-05 | 0.00287005 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578105 | CTTCCTTTGGTTTTC[C/T]CTAGGCTTCAACGCT | 6709 |
rs777372084 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128561932 | TAAGAGTAAAATATG[G/T]TCTTCTTTAGAGTTC | 6709 |
rs777375392 | snp | C/T | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554181 | TTACTCAAAGGGACC[C/T]TCAAAGTGTGTTAAC | 6709 |
rs777380509 | in-del | -/TTTC | 1.64727e-05 | 0.00286986 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618847 | GAGATTATGGCTGAT[-/TTTC]TTCCTGTCTCCTGTA | 6709 |
rs777407223 | snp | C/G | 1.66125e-05 | 0.00288201 | missense | SPTAN1 | GRCh38.p7 | 9:128624417 | TGCAGCCCAGAGAAA[C/G]GCGAAGCTGGATGAG | 6709 |
rs777409812 | in-del | -/GCGGAGGCC | | | utr-variant-5-prime | SPTAN1 | GRCh38.p7 | 9:128552618 | AGTGAACGGTGTGGA[-/GCGGAGGCC]GCGGAGGCCGCGGAG | 6709 |
rs777412539 | snp | C/T | 1.65723e-05 | 0.00287852 | stop-gained | SPTAN1 | GRCh38.p7 | 9:128611723 | TTTTAGAGCAAGCAC[C/T]AGAAGCACCAGGCTT | 6709 |
rs777439095 | in-del | -/GGTCCCC | 5.4308e-05 | 0.00521067 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628127 | TAGCCCATGGTCCCT[-/GGTCCCC]GGTCCCCGATAGAGC | 6709 |
rs777441722 | snp | C/G/T | 4.96959e-05 | 0.00498456 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128588922 | GGGAGATATCCTTAC[C/G/T]TTACTCAACAGCACC | 6709 |
rs777467378 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585609 | CTGAGCCTCTCAAAA[A/C]AAATGGAATTATGAA | 6709 |
rs777468752 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584612 | GTCAGGATGGGCAGG[A/G]TCGAATTTAAATTAT | 6709 |
rs777478835 | snp | C/T | 8.37991e-05 | 0.00647244 | downstream-variant-500B, synonymous-codon | SPTAN1, WDR34 | GRCh38.p7 | 9:128633786 | GTCCAGGTCCTCAGC[C/T]TCCCGGGGCCCTTGT | 6709 |
rs777505164 | snp | A/G/T | 4.95179e-05 | 0.00497563 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632521 | CTGGCTGGGTGGGGG[A/G/T]TGTTCGGCAGCAGGG | 6709 |
rs777551155 | snp | C/T | 1.64781e-05 | 0.00287033 | missense | SPTAN1 | GRCh38.p7 | 9:128568857 | ATGAAACTGGAAACC[C/T]GATGATCTCAGAAGG | 6709 |
rs777555495 | snp | A/C | 1.6525e-05 | 0.00287441 | missense, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633269 | CCCTACGTGGACGGC[A/C]AGGGCCGCGAGCTCC | 6709 |
rs777559634 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617930 | TTTCCTGGGAGCTTC[A/G]AGACAGAAGCACCAG | 6709 |
rs777564337 | snp | A/G | 1.66352e-05 | 0.00288398 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575377 | TGTATGCTTCTCACA[A/G]CATTATTATGTTAAC | 6709 |
rs777571266 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576312 | TCTACTCAGACTCAG[A/G]CTGACAAGACAGGAT | 6709 |
rs777591131 | snp | A/C | 1.64876e-05 | 0.00287116 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607826 | ATCTGCTGCCAGTTA[A/C]CTAATCCCTTCCCTC | 6709 |
rs777596672 | snp | C/T | 1.65002e-05 | 0.00287225 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632458 | TGTGACTGAGGAGGC[C/T]CTCAAAGAATTCAGC | 6709 |
rs777617281 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610756 | CCATCCTTCTCCTAG[C/T]CCTTTCATTTCCCAG | 6709 |
rs777617542 | snp | A/G | 4.94254e-05 | 0.00497094 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128599016 | CTGTGTGTGGATCTT[A/G]AACATGAGAAGGACT | 6709 |
rs777632874 | in-del | -/TT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623622 | ACCAAACCTGGCTAA[-/TT]TTTTTTTTTTTTTTT | 6709 |
rs777652619 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568392 | TTTTCAAGAGTAAGC[A/G]CTGAATGTTGAGAAA | 6709 |
rs777687384 | in-del | -/T | 1.64781e-05 | 0.00287033 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582586 | TCTTCATGCTCCTCC[-/T]TTTTGGTACATGAAT | 6709 |
rs777701049 | snp | A/G | 0.000107521 | 0.00733137 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627635 | AGCTGGGCTGGCAAC[A/G]CCTGGTCGGGCTCTG | 6709 |
rs777702782 | snp | A/G | 1.6476e-05 | 0.00287014 | missense | SPTAN1 | GRCh38.p7 | 9:128584841 | ATGCCATGGTGGAGG[A/G]AGGTGAGTGATTGGT | 6709 |
rs777707442 | snp | A/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128612113 | CTGTTCCCCAGGCCC[A/G]CCTGGCTGCCTTAGC | 6709 |
rs777716023 | snp | A/G | 1.64871e-05 | 0.00287111 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128583813 | TCGTGAAGCCAACCA[A/G]CAACAGCAATTTAAT | 6709 |
rs777747098 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565765 | TCCAGGGTAACACAA[C/T]TTTATACCTTTTATT | 6709 |
rs777754916 | snp | C/T | 1.7433e-05 | 0.00295232 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628161 | CAAGCCAGGGGGAGC[C/T]GTCCTTGCCTCACTG | 6709 |
rs777780283 | snp | C/G | 1.64885e-05 | 0.00287123 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128618016 | TGGCAAGAAGCTGTC[C/G]GATGACAACACCATC | 6709 |
rs777801455 | snp | C/T | 3.30502e-05 | 0.00406497 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128608900 | TGCTGCTCTGCAGGC[C/T]TTTGCCGACCAGCTC | 6709 |
rs777809136 | snp | A/G | 1.64906e-05 | 0.00287142 | missense | SPTAN1 | GRCh38.p7 | 9:128582803 | CTGATGAGCTCAAGA[A/G]TTGGGTCAATGAGAA | 6709 |
rs777816678 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633439 | AACCTTAAGCCTGCT[G/T]AGCTTGGAATAAGAC | 6709 |
rs777827536 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128598875 | TTTTGGAATTATCTC[C/G]TGTGTTTCCAGGTTT | 6709 |
rs777852931 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128602790 | ACAGGCTCACACCAC[C/T]GTGCCCAGCTAATTT | 6709 |
rs777869857 | snp | A/G | 2.62292e-05 | 0.00362131 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628238 | AAGGCCAGAGCTGGA[A/G]TCCAGAGGCCCTAAG | 6709 |
rs777872032 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633394 | CCTTGCTGCATGTCC[A/G]CTCCTCTGTGTGCTC | 6709 |
rs777889951 | snp | C/T | 1.65272e-05 | 0.0028746 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608294 | GAGGCCTCTGGACCA[C/T]GGAGTTGGAGTCTGG | 6709 |
rs777891526 | snp | C/G | 1.6819e-05 | 0.00289987 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613511 | GGAGGCGGGCCAGGC[C/G]CGAGTGCCTGGGACA | 6709 |
rs777912157 | snp | A/G | 1.64776e-05 | 0.00287028 | missense | SPTAN1 | GRCh38.p7 | 9:128605113 | GGACATGATCTCGCC[A/G]GTGTCCAGGCCCTGC | 6709 |
rs777926067 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623803 | ATTAATTCCTTGGAC[C/T]GGCTGGGCACTATGG | 6709 |
rs777942959 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128575207 | TGAATAGGAAGCAAT[C/T]GTTACTTCTGAAGAG | 6709 |
rs777950008 | snp | A/G | 4.94303e-05 | 0.00497119 | missense | SPTAN1 | GRCh38.p7 | 9:128625850 | GATCAGCTTCTCGCC[A/G]CCAAACACGTTCAGT | 6709 |
rs777952957 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128619541 | TCTGCCTGTCTTCAC[A/G]TAGCCATCTTCCCTC | 6709 |
rs777957971 | snp | C/T | 6.60426e-05 | 0.00574604 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578253 | AGCACAAGGTAATGG[C/T]ATCTCTAGAATCTTC | 6709 |
rs778017183 | in-del | -/AG | 0.000135333 | 0.00822485 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632980 | TCAGGAGGTGGGTGA[-/AG]AGGTGTCCTTTGGAA | 6709 |
rs778020180 | snp | C/G | 1.65081e-05 | 0.00287293 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581077 | AATCTGTGAGCAAAG[C/G]CTTGCCAGTGGTGGG | 6709 |
rs778023109 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559340 | GGGCCCAAGCAGGGG[A/G]ACTTGCTCAGATGGA | 6709 |
rs778038290 | in-del | -/CAAAAAA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563412 | AGAGTGAGACCCTGC[-/CAAAAAA]CAAAAAACAAAAAAA | 6709 |
rs778052773 | snp | A/C | 3.48123e-05 | 0.00417192 | downstream-variant-500B, utr-variant-3-prime | SPTAN1, WDR34 | GRCh38.p7 | 9:128633726 | CAGCGAAGGCTTGCA[A/C]CCGCCTCCCGGGACC | 6709 |
rs778117550 | snp | A/G | 1.66969e-05 | 0.00288932 | missense | SPTAN1 | GRCh38.p7 | 9:128577488 | CAGAGAGACATGCAC[A/G]GCTCAATGATTCATA | 6709 |
rs778118274 | snp | G/T | 1.64787e-05 | 0.00287038 | missense | SPTAN1 | GRCh38.p7 | 9:128583958 | CTAGAGGCAGATGTG[G/T]CTGCTCACCAGGTAG | 6709 |
rs778121117 | snp | C/T | 1.6476e-05 | 0.00287014 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128582556 | CACTCGCCGAGATGC[C/T]GTAAGTTTGTAGGTT | 6709 |
rs778125604 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582047 | GACATGCTATCTCGT[C/T]GAAGACATAATACAA | 6709 |
rs778129817 | snp | C/T | 1.65488e-05 | 0.00287647 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632856 | TTTCATGATCAGCCG[C/T]GAAACTGAGAACGTC | 6709 |
rs778134606 | snp | C/T | 1.65217e-05 | 0.00287412 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632742 | ATTAAGGCCAGGTGC[C/T]GTGAGCCTCTGCCCG | 6709 |
rs778145394 | snp | A/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557139 | TTTTTCCATAACCAA[A/T]TGACCAAACGACCCG | 6709 |
rs778148136 | snp | C/T | 0.000185808 | 0.00963688 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621281 | GCCCATTGGTAAGAC[C/T]TCCATCGCCCACTGG | 6709 |
rs778185606 | snp | G/T | 1.67911e-05 | 0.00289746 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605520 | TGGAACATAGAGCCT[G/T]CTTTGTAGGGGTCAT | 6709 |
rs778234195 | snp | A/G | 1.81721e-05 | 0.00301425 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627614 | CCAGAGGCAGCCTGG[A/G]AATAAAGCTGGGCTG | 6709 |
rs778253971 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569446 | GGAACTCTTTGGTCT[C/G]GCTGATTTTAGTGCG | 6709 |
rs778305895 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617829 | GGGACAGACAAACCC[C/T]TTGCGCTTATTTCAC | 6709 |
rs778308337 | snp | G/T | | | downstream-variant-500B, missense | SPTAN1, WDR34 | GRCh38.p7 | 9:128633956 | GTTTCTGGGAGCTTT[G/T]CTGGAGATCAAACAG | 6709 |
rs778320434 | snp | C/G | 1.65053e-05 | 0.0028727 | missense | SPTAN1 | GRCh38.p7 | 9:128566810 | CGGCAGCAGGTCCTA[C/G]ACCGATACCACCGCT | 6709 |
rs778328513 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595979 | CTCCTGAGTAGCTGG[C/G]ATTATAGGTATGCAC | 6709 |
rs778341217 | in-del | -/AAA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590548 | ATCTCTATTTATATT[-/AAA]AAAGAAAAAAAAAAA | 6709 |
rs778371814 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128614967 | GTTCTATATGTTGAC[A/C]CATGTGATTATATGA | 6709 |
rs778372200 | snp | A/G | 1.64876e-05 | 0.00287116 | missense | SPTAN1 | GRCh38.p7 | 9:128587654 | GATCTCAGTGCCTAC[A/G]GCAGCAGCATCCAGG | 6709 |
rs778373476 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128570846 | TTGTATTTTTAGTAG[A/G]GACAGGGTTTCTCCA | 6709 |
rs778379868 | snp | C/G | 1.66635e-05 | 0.00288643 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587569 | GATGGGAGGCTTCAG[C/G]CCCTGCACAGTGCTC | 6709 |
rs778399884 | snp | A/T | 4.94262e-05 | 0.00497098 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578092 | GGAAACATAATGTCT[A/T]CCTTTGGTTTTCCCT | 6709 |
rs778408492 | snp | C/G | 1.6477e-05 | 0.00287024 | missense | SPTAN1 | GRCh38.p7 | 9:128577358 | CATTTCTAGGTCAAA[C/G]CCCTGTGTGCTGAGG | 6709 |
rs778422165 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632979 | CTCAGGAGGTGGGTG[A/G]AGAGGTGTCCTTTGG | 6709 |
rs778430625 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558075 | CCCAAAGTGCTGGGA[G/T]TACAGGCGTGAGCCA | 6709 |
rs778485437 | in-del | -/GGCC | 1.65952e-05 | 0.00288051 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617767 | CTATTCAGGTAAGGA[-/GGCC]GGCCGCCTTCTGGCC | 6709 |
rs778485732 | snp | C/G | 0.000115368 | 0.00759412 | missense | SPTAN1 | GRCh38.p7 | 9:128582782 | TGCAGCAGTTTTTCC[C/G]TGATTCTGATGAGCT | 6709 |
rs778486203 | in-del | -/AG | 1.64987e-05 | 0.00287212 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605231 | TGCCCCAGAAAGAGC[-/AG]AGTCTTCTGTTCTGC | 6709 |
rs778489951 | snp | A/G | 3.29506e-05 | 0.00405884 | missense | SPTAN1 | GRCh38.p7 | 9:128582710 | TGTTGAGCCGCCGCA[A/G]TGCCCTTCACGAGAG | 6709 |
rs778507284 | snp | C/T | | | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128551944 | CTCTCACCACCTCCT[C/T]AAACCCGGGGCCCCA | 6709 |
rs778513605 | in-del | -/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607120 | ACTGGATCAAATGTA[-/T]GCCCAGGCCTAGGGC | 6709 |
rs778514973 | snp | A/G | 1.66621e-05 | 0.00288631 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624290 | AGGTAACCACAGCAG[A/G]TAAGGCTGACCAGTG | 6709 |
rs778518443 | in-del | -/TAACT | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128553401 | GTGGCTCAAATCAAA[-/TAACT]TAACTTAATAGCTTA | 6709 |
rs778521010 | snp | A/G | 8.82729e-05 | 0.00664294 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627204 | TTGAAGCCCCTGGGG[A/G]GTGGGAACAGAGAAA | 6709 |
rs778546731 | snp | C/T | 0.000100246 | 0.00707904 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617810 | GTGTTTGAGTGGGCC[C/T]CAGGGGACAGACAAA | 6709 |
rs778555189 | snp | A/G | 3.10304e-05 | 0.00393881 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604456 | GAGAGGGAGAAACAG[A/G]TGACTGCTGGTTTCC | 6709 |
rs778570395 | snp | A/G | 4.98865e-05 | 0.00499407 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128585710 | CTGTGATGTGTCAAC[A/G]TAGTTTTTGTTATCC | 6709 |
rs778595535 | snp | A/G | | | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128554086 | AATTGAATGTGCTGC[A/G]GAGGAAAAAAAAAGT | 6709 |
rs778612773 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628521 | TGTGATAGACAGGAC[A/G]TGGGAGGAGCCCCAG | 6709 |
rs778617132 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597753 | GCACCCCGGTTCAAG[C/T]GATTCTCCTGCCTCA | 6709 |
rs778630836 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128595899 | CCCAGGCTGGAGTGC[A/G]GTGGCCCAGTCTCGG | 6709 |
rs778659956 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616921 | TAGGCGACAGAGCAA[G/T]ACTTTGTCTCAAAAA | 6709 |
rs778684585 | snp | C/T | 1.68066e-05 | 0.00289879 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577510 | TGATTCATACAGGTG[C/T]AAATAATGCTCCAGG | 6709 |
rs778695725 | snp | A/G | 3.29832e-05 | 0.00406085 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128580951 | CGAGGAGAGAGCGGC[A/G]CTGCTGGAGCTGTGG | 6709 |
rs778699458 | snp | C/T | 1.65512e-05 | 0.00287669 | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633367 | CCACCCCTCGCTGCT[C/T]GCCCTGCGTCGCCTT | 6709 |
rs778709187 | snp | A/T | 1.65894e-05 | 0.00288 | | | GRCh38.p7 | 9:128624399 | GTCAGACCTGGAGAA[A/T]GCTGCAGCCCAGAGA | 6709 |
rs778711282 | snp | G/T | 0.000151974 | 0.00871574 | | | GRCh38.p7 | 9:128613520 | CCAGGCCCGAGTGCC[G/T]GGGACACAGCTCTGC | 6709 |
rs778720590 | snp | A/G | 0.000362402 | 0.0134562 | | | GRCh38.p7 | 9:128578088 | CGCTGGAAACATAAT[A/G]TCTTCCTTTGGTTTT | 6709 |
rs778743322 | snp | A/G | 6.44406e-05 | 0.00567593 | | | GRCh38.p7 | 9:128609376 | TAAAACAATCTCCTT[A/G]CACCCATGGGAAGTC | 6709 |
rs778787847 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | SPTAN1 | GRCh38.p7 | 9:128575202 | GTCCCTGAATAGGAA[A/G]CAATTGTTACTTCTG | 6709 |
rs778813056 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128610560 | ACTGCCTTTTAGTTG[G/T]TTTTTTTTTGCCCCC | 6709 |
rs778825447 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625021 | TGTACACAAAAAATG[C/G]TTTGTCTGGGTTTTG | 6709 |
rs778853648 | snp | G/T | 1.66679e-05 | 0.00288681 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587564 | TGGAGGATGGGAGGC[G/T]TCAGCCCCTGCACAG | 6709 |
rs778867130 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128623461 | AATTTCAGCCCATTC[A/G]TTTTTTTTGTTTGAG | 6709 |
rs778891011 | snp | C/T | 1.65875e-05 | 0.00287984 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575362 | TAAATAGCAAAGTGC[C/T]GTATGCTTCTCACAA | 6709 |
rs778905676 | in-del | -/CT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558252 | TCCTGCTTTATCCCC[-/CT]GAGATTCGCATTACT | 6709 |
rs778917848 | snp | C/T | 3.29538e-05 | 0.00405904 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128625846 | CAAAGATCAGCTTCT[C/T]GCCGCCAAACACGTT | 6709 |
rs778922622 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128631652 | TCAATGCAGTGAAAC[A/G]TCGCCTCTACTAAAA | 6709 |
rs778930540 | snp | A/T | 1.69109e-05 | 0.00290778 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613339 | CAGAATGCTGAGTAT[A/T]CACCACACAGTAGCC | 6709 |
rs778937633 | snp | A/G | 3.29745e-05 | 0.00406031 | missense | SPTAN1 | GRCh38.p7 | 9:128617999 | CAGGGTGTCCTGGAC[A/G]CTGGCAAGAAGCTGT | 6709 |
rs778949349 | snp | C/T | 3.3112e-05 | 0.00406877 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608866 | CTCATGCCTTTGTTT[C/T]CTGACAGGAAGAGAA | 6709 |
rs778979270 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589076 | TGAGTTTCCTCACCA[A/G]TCCCCCACGTGACAT | 6709 |
rs778996907 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128558355 | TCTAATAATATTTTG[C/T]AAATATATACCTTTT | 6709 |
rs779020422 | snp | A/G | 1.64732e-05 | 0.0028699 | missense | SPTAN1 | GRCh38.p7 | 9:128612130 | CTGGCTGCCTTAGCT[A/G]ACCAGTGGCAGTTCT | 6709 |
rs779020642 | snp | C/T | 3.32784e-05 | 0.00407898 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621133 | GCAGGCTCTCAATAG[C/T]GTGCCTTGGCTGCTT | 6709 |
rs779071125 | snp | A/G | 6.60251e-05 | 0.00574528 | missense | SPTAN1 | GRCh38.p7 | 9:128566789 | GCAGAGGACATCCAG[A/G]AGAGGCGGCAGCAGG | 6709 |
rs779072307 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557020 | GGCATCCTAAGCCAC[A/G]GAAAAAAGACATTGT | 6709 |
rs779083749 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128569080 | AGCATGAATGCAAGC[A/G]TTTGTATACTCAGTG | 6709 |
rs779106921 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633657 | TAAATGATGACTTCC[C/G]CCAAAGCTTTGCTTT | 6709 |
rs779143018 | snp | A/G | 0.000193086 | 0.00982373 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128604361 | GTCCCTACAGCAGCT[A/G]GCCGAGGAACGGAGC | 6709 |
rs779152265 | snp | C/T | 3.29451e-05 | 0.00405851 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128581796 | GGCGTTCCTGTTGAA[C/T]GAAGACTTGGGAGAT | 6709 |
rs779157129 | snp | A/C | 0.00016214 | 0.00900244 | intron-variant, upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128555330 | GCTTGTTATCTTGCT[A/C]TTCCCCCTCCCTCTT | 6709 |
rs779164586 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627274 | CCTCCTCCTCTCATC[G/T]TTGGGGAGGTTCCTT | 6709 |
rs779214627 | snp | A/G | 3.30246e-05 | 0.0040634 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608279 | GATTAACGTCCAGGT[A/G]AGGCCTCTGGACCAT | 6709 |
rs779226167 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128594274 | GAATGAACTACAGCA[A/G]TGGATCAATGAGAAG | 6709 |
rs779243551 | snp | C/T | 1.64849e-05 | 0.00287092 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128587647 | GATGTCAGATCTCAG[C/T]GCCTACGGCAGCAGC | 6709 |
rs779260779 | snp | C/T | 1.6477e-05 | 0.00287024 | missense | SPTAN1 | GRCh38.p7 | 9:128582545 | GAAGATGTGGCCACT[C/T]GCCGAGATGCTGTAA | 6709 |
rs779263212 | snp | C/T | | | downstream-variant-500B, missense | SPTAN1, WDR34 | GRCh38.p7 | 9:128633833 | TCAGCTGCCACACCT[C/T]CACTGTGCCCTGGGC | 6709 |
rs779275704 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600646 | CTGACCAAGAATACA[A/G]GGAGAAGGTGTGTTT | 6709 |
rs779281086 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592171 | GAGTTTGGGTAGAAT[A/G]GTGAAATTTTTGGGC | 6709 |
rs779287362 | snp | C/G | 1.72901e-05 | 0.0029402 | downstream-variant-500B, intron-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128634012 | AGATACGTGGAGTAA[C/G]AGAAACTCTAGAGAC | 6709 |
rs779287600 | snp | A/G | 1.68559e-05 | 0.00290304 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625223 | ATGTATGCAGATAGC[A/G]TCTGTGAGATGACTG | 6709 |
rs779362940 | snp | A/G | | | upstream-variant-2KB | SPTAN1 | GRCh38.p7 | 9:128551519 | CTAGCTCTTCCAATT[A/G]GTAGCTGCCTGACCT | 6709 |
rs779363037 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128606869 | CCAATGACATTTAAT[A/G]TATTCACGGTGTTGT | 6709 |
rs779387603 | snp | A/G | 1.65209e-05 | 0.00287405 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632384 | GGAAAAGACACAGTC[A/G]CCTGCTGTGTGGAGG | 6709 |
rs779393161 | snp | C/T | 8.23852e-05 | 0.00641762 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128618970 | GACCCTGGTGGCCAG[C/T]GAAGATTATGGCGAC | 6709 |
rs779393978 | snp | A/C | 1.64795e-05 | 0.00287045 | missense | SPTAN1 | GRCh38.p7 | 9:128609247 | AAAAATTGCAAACAG[A/C]GAGTGATGAGTCGTA | 6709 |
rs779444978 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628485 | TGTCCGCCCTAATAG[A/G]AGGCAAAAATGCACC | 6709 |
rs779464651 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128567964 | ACAGGATTTCATCAT[G/T]TTTGCCAGGCTGGTT | 6709 |
rs779472865 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613614 | CATTCTCAAAGGTTG[G/T]GGCCTCAGGATCATT | 6709 |
rs779483712 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593969 | ACCTGGTTGTGAACA[A/G]TACAGTGTGCGCATA | 6709 |
rs779508833 | snp | C/G | 0.000186079 | 0.00964391 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128609370 | CATTTATAAAACAAT[C/G]TCCTTGCACCCATGG | 6709 |
rs779534151 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128563477 | TGGTCAATCCAAGAT[G/T]GGTAATTCAGATTTA | 6709 |
rs779536006 | snp | A/G/T | 3.29453e-05 | 0.00405854 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128577125 | TGGTGCCTTTGTTCT[A/G/T]TAGGGATGTGGATGA | 6709 |
rs779587514 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565444 | GAGAATAATTTAAAG[A/G]AATGGTGATATGACT | 6709 |
rs779604771 | snp | G/T | 1.64773e-05 | 0.00287026 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128607571 | CCTTACCAGGTAATA[G/T]AATAGCTATTTTTCT | 6709 |
rs779622426 | snp | A/G | 3.30382e-05 | 0.00406423 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584574 | GGGAAAGGCTGTGCT[A/G]TTGTAGCATAAAGGG | 6709 |
rs779633188 | snp | A/G | 1.64738e-05 | 0.00286995 | missense | SPTAN1 | GRCh38.p7 | 9:128584799 | CTGGACATGAACCAC[A/G]CATCAAAGCAGTTAC | 6709 |
rs779640676 | snp | C/G | 3.29451e-05 | 0.00405851 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575179 | TTGGTGACTCTGGCT[C/G]TCTTATGGTCCCTGA | 6709 |
rs779648483 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564421 | AAGAGTCCTTCTCAG[A/G]AAAAAAAAAAAAATT | 6709 |
rs779648804 | snp | A/T | 6.59283e-05 | 0.00574106 | missense | SPTAN1 | GRCh38.p7 | 9:128577391 | GACCGCCTGCAACAG[A/T]CCCACCCTCTGAGTG | 6709 |
rs779668439 | snp | A/G | 1.66252e-05 | 0.00288311 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625189 | AAACAGGTCTGCCCT[A/G]GCCCCTTCACTGGTT | 6709 |
rs779671606 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128597620 | TACCTGTTGAACAGA[C/T]CCTTATAGCTTTTTT | 6709 |
rs779673690 | snp | A/G | 1.65954e-05 | 0.00288053 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626719 | CCTCAGGAGCTGCTC[A/G]GCCTCCCAGAGCCCT | 6709 |
rs779675620 | snp | A/G | 3.80098e-05 | 0.0043593 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583322 | ACATGCATGTTTGGG[A/G]AACTAAATACCCCTT | 6709 |
rs779682224 | snp | A/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128605344 | ATCCAGTCCCATCCC[A/G]AGTCAGCAGAAGACC | 6709 |
rs779728504 | in-del | -/A | 1.65179e-05 | 0.00287379 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584547 | CTGCTTCCCTCAGGT[-/A]GGAATCAACTTGGGA | 6709 |
rs779738397 | snp | G/T | 3.29533e-05 | 0.00405901 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582580 | GTAGGTTCTTCATGC[G/T]CCTCCTTTTTGGTAC | 6709 |
rs779753950 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608527 | TAAGGGAATAATGAA[C/T]AAACAACAAGGAAGA | 6709 |
rs779758358 | snp | C/G | 1.66454e-05 | 0.00288486 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128628058 | TGCCCAGGGCGGGCT[C/G]CACTTCCCCTCCCAC | 6709 |
rs779759134 | snp | A/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128591549 | AAGAAATTGGACCCC[A/G]CCCAGTCAGCCTCCC | 6709 |
rs779773139 | in-del | -/C | 0.000808607 | 0.020091 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630423 | CCCTTCACCCAGCCA[-/C]CCCCCCAGGGTACCC | 6709 |
rs779777414 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576381 | CTCAAAAAAGAAAAA[A/C]AGAAATGTCGTCAGT | 6709 |
rs779824616 | in-del | -/AAACTGAGAACGTCAA | 1.65509e-05 | 0.00287666 | frameshift-variant | SPTAN1 | GRCh38.p7 | 9:128632858 | TCATGATCAGCCGCG[-/AAACTGAGAACGTCAA]GTCCAGCGAGGAGAT | 6709 |
rs779831676 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622261 | GATCACCAGTGTGAG[C/T]GTCCTTCAGCCTCCT | 6709 |
rs779838514 | snp | C/G | 4.99913e-05 | 0.00499931 | missense | SPTAN1 | GRCh38.p7 | 9:128583224 | GATGAAGTGGCAGCT[C/G]GTATGAATGAGGTGA | 6709 |
rs779860810 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128587825 | ACACAAAGATTTACA[A/G]AGTTTAAAATAAGAT | 6709 |
rs779869876 | snp | C/T | 4.97574e-05 | 0.00498761 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128621149 | GTGCCTTGGCTGCTT[C/T]TACTCCAGGGCTTAC | 6709 |
rs779870022 | snp | G/T | 0.000980873 | 0.0221241 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627183 | CCCTCCAGGTCCGCC[G/T]CTTCCTTGAAGCCCC | 6709 |
rs779878893 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580772 | TTGAACATGCACATA[C/G]AAGTGAATGTTGTTT | 6709 |
rs779895535 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620793 | CCTTAAAAATGTGTC[A/G]TTTTTGTTTGGGTGT | 6709 |
rs779899640 | snp | C/T | 3.29451e-05 | 0.00405851 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591458 | AATTTACTTTCAGTT[C/T]TCCCTCTTTTTTCCT | 6709 |
rs779973472 | snp | C/T | 1.64866e-05 | 0.00287106 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128617682 | GGACTACGGCCGGGA[C/T]CTAACCGGCGTGCAG | 6709 |
rs779982346 | snp | A/C/T | 4.94176e-05 | 0.00497059 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128603566 | TCTGATGGTTCACAC[A/C/T]GTGGCCACCTTTAAT | 6709 |
rs779988474 | snp | C/T | 1.64991e-05 | 0.00287215 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128608267 | CTTTGACAAAGCGAT[C/T]AACGTCCAGGTGAGG | 6709 |
rs779993051 | snp | C/T | 0.000115305 | 0.00759205 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128591548 | GAAGAAATTGGACCC[C/T]GCCCAGTCAGCCTCC | 6709 |
rs780033700 | snp | C/T | 1.65452e-05 | 0.00287616 | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633344 | AACTGAGCCACTCCC[C/T]GGGTCACCCACCCCT | 6709 |
rs780037227 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128557320 | TTGTTTTTAATAGAG[A/G]CTCCTTTCAGCTTCA | 6709 |
rs780043888 | snp | C/T | 1.64792e-05 | 0.00287042 | missense | SPTAN1 | GRCh38.p7 | 9:128625830 | CCAACATCACTGCCC[C/T]CAAAGATCAGCTTCT | 6709 |
rs780063023 | snp | A/G | 1.68986e-05 | 0.00290672 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618139 | CAGGAGCTCCCGGGA[A/G]CAAGTGGAAGGCCAG | 6709 |
rs780098694 | in-del | -/GGT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627576 | TTCCAGCCCCAAGGA[-/GGT]GGTGGTGGTGCTTTG | 6709 |
rs780109573 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128556869 | TTTTGAGTTAATTTT[A/G]TTTGATCTGAGAATC | 6709 |
rs780119206 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580824 | AAAAGGCCTGAAGAT[C/T]AGCACTAGGATTAGG | 6709 |
rs780124719 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128568720 | AACAGCGGGGACAAA[A/G]TGCTGATGCTGTGTG | 6709 |
rs780150883 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575445 | CCCCTAATTTCTGAG[C/T]GAGCAAGTTTTTGTA | 6709 |
rs780159478 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128618931 | CAATGTGGAAGAGGA[A/G]GAAGCCTGGATCAAT | 6709 |
rs780165307 | in-del | -/TTT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586113 | CCATTTTTCACTTGG[-/TTT]TTTTTTTTTTTTTTT | 6709 |
rs780184944 | snp | A/G | 5.23894e-05 | 0.00511781 | missense | SPTAN1 | GRCh38.p7 | 9:128604339 | AGGAGCTGAATGAGC[A/G]CTGGCGGTCCCTACA | 6709 |
rs780213263 | snp | A/G | 1.6495e-05 | 0.0028718 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632611 | CAGGCTGAACCATCA[A/G]GAGTTCAAATCTTGC | 6709 |
rs780217401 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612766 | TCCTGTCTCTACTAA[A/G]AATACAAAAATTAGC | 6709 |
rs780225297 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128555725 | TGTAGTGTTTGCTGA[C/G]TTTTTATTGGTGGCT | 6709 |
rs780240670 | in-del | -/T | 1.64746e-05 | 0.00287002 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600070 | CTAAATTCCTCTTTC[-/T]TTTGAATAGGATGAA | 6709 |
rs780286059 | snp | A/G | 1.65405e-05 | 0.00287576 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584009 | TGGGCAAGTGAATGC[A/G]GAAACTATAGGAGGG | 6709 |
rs780295590 | snp | A/G | 0.000250294 | 0.0111841 | missense | SPTAN1 | GRCh38.p7 | 9:128576919 | CTGCAGAGGCAGGGG[A/G]AGCTCTTTGGGGCAG | 6709 |
rs780295648 | snp | G/T | 1.65455e-05 | 0.00287619 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581913 | ACCCCTTCTTGTCAG[G/T]GCTTTCAAATGACCC | 6709 |
rs780303413 | snp | G/T | 3.2969e-05 | 0.00405998 | missense | SPTAN1 | GRCh38.p7 | 9:128585907 | CTGAATCCTGGATGC[G/T]GGAGAAGGAACCCAT | 6709 |
rs780312780 | snp | A/C | 1.64732e-05 | 0.0028699 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627989 | GTCATGTGGGGGTCT[A/C]GTGCGCTTGCCCCTC | 6709 |
rs780333914 | snp | C/T | 1.65184e-05 | 0.00287384 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574629 | AAGAGCCAGATCCCA[C/T]AGAGCCAGTTGTGAT | 6709 |
rs780351957 | snp | C/G | 1.64806e-05 | 0.00287054 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612103 | TGGCTCCCTTCTGTT[C/G]CCCAGGCCCGCCTGG | 6709 |
rs780352316 | snp | A/G | 1.64732e-05 | 0.0028699 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630283 | GCTCTCGGCCAGCTG[A/G]GAGCAGGCCCCTTTC | 6709 |
rs780356981 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612330 | GTGCCCAAAACCACG[A/G]AAAGGCAGGGCTCAC | 6709 |
rs780358723 | snp | G/T | 1.64738e-05 | 0.00286995 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608102 | GCTGAAGGGCCTCAT[G/T]TTCTCACCTGCCTCT | 6709 |
rs780369680 | snp | A/G | 1.65141e-05 | 0.00287346 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605253 | TCTGTTCTGCAGAGC[A/G]TACCCCCTTACTGCA | 6709 |
rs780374369 | snp | C/G | 1.6473e-05 | 0.00286988 | missense | SPTAN1 | GRCh38.p7 | 9:128594221 | CGTAAAGGCATGTTG[C/G]AGAAGAGTTGCAAGA | 6709 |
rs780417994 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626331 | CGCACCCCACCTCCT[G/T]CACTGCGTCGGCACG | 6709 |
rs780419601 | snp | A/G | 1.64866e-05 | 0.00287106 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128568807 | AGCATTTGAAGCTGA[A/G]GTGCAGGCCAACTCA | 6709 |
rs780433514 | snp | A/G | 1.64912e-05 | 0.00287147 | missense | SPTAN1 | GRCh38.p7 | 9:128608964 | TCTAGCCGGCGCAAT[A/G]AGGTCTTGGACAGGT | 6709 |
rs780450163 | snp | C/T | 3.50109e-05 | 0.00418381 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630149 | AGAAATGCTCCCTGC[C/T]ATCCCTCGATCCCTG | 6709 |
rs780460157 | snp | C/T | 1.64846e-05 | 0.0028709 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128588868 | CTTGGCTCTCTACGA[C/T]TATCAGGAGAAGAGT | 6709 |
rs780477971 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584918 | CGAGGGCATGGCCAC[A/G]TGGGCATCACAAACC | 6709 |
rs780506377 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128629985 | TCCCCCACATGGCTG[C/G]AGAGAGGATGCTCAG | 6709 |
rs780506791 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564285 | TTAGCTAGGCACCAT[C/G]ATGGGCGCCTGTAAT | 6709 |
rs780519517 | snp | A/G | | | intron-variant, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633193 | CAGGCACCAGGTGCC[A/G]TCTCTTACCCCACAG | 6709 |
rs780530803 | snp | C/T | 6.59217e-05 | 0.00574078 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128615805 | TCGCCTGCACCAGTT[C/T]TTCCGGGACATGGAT | 6709 |
rs780535734 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562837 | GGGCGTGATGGCAGG[C/T]GCCTGTGGTCCCAGC | 6709 |
rs780538141 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604198 | TAATTTATTCAGCGA[A/G]GAAGGTTGGAAACAG | 6709 |
rs780579546 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128625353 | GGAAGCAGACACAGA[A/G]CCAGGCATCTCTGCA | 6709 |
rs780606741 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594066 | TCATCATTACAAACT[C/T]GTAGCCTGGAATCCA | 6709 |
rs780622472 | snp | A/G | 4.94328e-05 | 0.00497131 | missense | SPTAN1 | GRCh38.p7 | 9:128615722 | GACAAGAGGGACACC[A/G]TCAACGGGCGCTTCC | 6709 |
rs780641212 | snp | C/T | 1.64991e-05 | 0.00287215 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128605439 | CAAGGCAAAGTTGGG[C/T]GACTCCCACGACCTG | 6709 |
rs780658554 | snp | C/T | 8.25021e-05 | 0.00642217 | missense | SPTAN1 | GRCh38.p7 | 9:128584312 | ATCACCATTCAGGCC[C/T]GCCAGTTCCAAGATG | 6709 |
rs780658978 | snp | A/G | 3.2987e-05 | 0.00406108 | missense | SPTAN1 | GRCh38.p7 | 9:128617659 | AAGAAGCTGCTGGTG[A/G]GCTCAGAGGACTACG | 6709 |
rs780675617 | snp | A/G | 1.6727e-05 | 0.00289193 | downstream-variant-500B, synonymous-codon | SPTAN1, WDR34 | GRCh38.p7 | 9:128633807 | GGGCCCTTGTTCCGT[A/G]AACTCTGTGCTCAGC | 6709 |
rs780696613 | snp | C/T | 3.35937e-05 | 0.00409826 | missense | SPTAN1 | GRCh38.p7 | 9:128626589 | CTGGCCGAGCTGGAC[C/T]GCCAGATCAAGAGCT | 6709 |
rs780733897 | snp | C/T | 4.94214e-05 | 0.00497074 | missense | SPTAN1 | GRCh38.p7 | 9:128609129 | TCTTTCAGGTGGCGA[C/T]GTCTGAAAGCCCAGA | 6709 |
rs780737544 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128562665 | AAAATAGGCTGACAG[A/G]CTTAGGGCAGCAGTG | 6709 |
rs780746382 | snp | A/C | 1.64727e-05 | 0.00286986 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128591454 | AAGGAATTTACTTTC[A/C]GTTCTCCCTCTTTTT | 6709 |
rs780750895 | snp | A/G | 1.65542e-05 | 0.00287695 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128625176 | GACGCTCCTCACCAA[A/G]CAGGTCTGCCCTGGC | 6709 |
rs780759979 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | SPTAN1 | GRCh38.p7 | 9:128591534 | CCGGCTGCGTACGTG[A/G]AGAAATTGGACCCCG | 6709 |
rs780780077 | snp | C/T | 1.65318e-05 | 0.002875 | synonymous-codon, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633325 | CACCCGCTCGCTTTT[C/T]GTGAACTGAGCCACT | 6709 |
rs780782090 | snp | A/G | 1.64751e-05 | 0.00287007 | missense | SPTAN1 | GRCh38.p7 | 9:128574804 | GACGTGATGGACTGG[A/G]TCAATGACAAGGCAC | 6709 |
rs780787520 | snp | A/C | 1.65181e-05 | 0.00287381 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128584550 | CTTCCCTCAGGTAGG[A/C]ATCAACTTGGGAAAG | 6709 |
rs780803421 | snp | C/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128564984 | TGTGAAGGTCCTGCT[C/G]AAGAGGTGGGTTCTT | 6709 |
rs780825737 | snp | C/T | 1.66629e-05 | 0.00288638 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128615851 | ATCAAGTATGTCTTC[C/T]CAGCCCTCTAGAAGG | 6709 |
rs780858157 | snp | C/T | 1.64798e-05 | 0.00287047 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128585875 | GGCCCAGCAGTACTT[C/T]GCTGATGCTAACGAG | 6709 |
rs780867742 | snp | C/T | 1.65037e-05 | 0.00287256 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574655 | GTGATCTGATTAAAA[C/T]TCTGATTTGAAACTT | 6709 |
rs780875433 | snp | A/G | 3.30764e-05 | 0.00406659 | missense | SPTAN1 | GRCh38.p7 | 9:128584442 | TGGCCGATTCTCTGC[A/G]GTTGCAGCAGCTCTT | 6709 |
rs780891902 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128575977 | AAGTGTATAAATCTG[C/T]TTATAGGCTGGTACT | 6709 |
rs780897019 | snp | C/G | 1.64966e-05 | 0.00287194 | missense | SPTAN1 | GRCh38.p7 | 9:128632592 | TTGACAAGGACAAGT[C/G]TGGCAGGCTGAACCA | 6709 |
rs780923276 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605742 | CACGTCTATAACCCC[A/G]GCACTTTGGTAGGCC | 6709 |
rs780963968 | in-del | -/AG | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586841 | TTTTTTTTCTGAGAC[-/AG]AGTCTCACTCTGTCA | 6709 |
rs780978085 | snp | C/T | 3.35689e-05 | 0.00409674 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128632204 | CGCCATGGAGGAGGC[C/T]CTCATCCTGGACAAC | 6709 |
rs780987125 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613215 | GAGAGTGTCTCAGGC[C/T]GGGCAGGCTGATTGG | 6709 |
rs781014486 | snp | A/G | 1.7063e-05 | 0.00292082 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627644 | GGCAACGCCTGGTCG[A/G]GCTCTGGAGCCGGGA | 6709 |
rs781021400 | snp | A/G | 4.94214e-05 | 0.00497074 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128600109 | CAAGACAGCCTCCCC[A/G]TGGAAGGTAAGAACT | 6709 |
rs781048881 | snp | G/T | 1.65015e-05 | 0.00287237 | missense | SPTAN1 | GRCh38.p7 | 9:128582813 | CAAGAGTTGGGTCAA[G/T]GAGAAGATGAAAACT | 6709 |
rs781052329 | in-del | -/CT | 0.277778 | 0.248452 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630241 | GGTTGCCAGGCATTG[-/CT]CTCTCTGAGAGAAGG | 6709 |
rs781083220 | snp | A/G | 3.29875e-05 | 0.00406112 | missense | SPTAN1 | GRCh38.p7 | 9:128618029 | TCCGATGACAACACC[A/G]TCGGGAAAGAGGAGA | 6709 |
rs781104763 | snp | A/C | 1.64879e-05 | 0.00287118 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128612091 | TTCATCTCTTTTTGG[A/C]TCCCTTCTGTTCCCC | 6709 |
rs781122568 | snp | C/G | 1.74233e-05 | 0.0029515 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624525 | GGAAGAGCCTTCCCA[C/G]AGCTGCTCTTTGTCT | 6709 |
rs781124530 | snp | C/G | 1.64727e-05 | 0.00286986 | missense | SPTAN1 | GRCh38.p7 | 9:128603550 | CTACCTAGTCTGCTC[C/G]TCTGATGGTTCACAC | 6709 |
rs781138053 | in-del | -/CTC | 1.73033e-05 | 0.00294132 | downstream-variant-500B, intron-variant | SPTAN1, WDR34 | GRCh38.p7 | 9:128634017 | GTGGAGTAAGAGAAA[-/CTC]CTCTAGAGACCAACC | 6709 |
rs781164969 | in-del | -/TTTA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128622741 | TTGTAGTATGGTTTA[-/TTTA]TTTATTTATTTATTT | 6709 |
rs781170748 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578517 | CTACTACTTGGCACA[C/T]TGATCCTTTGTGATG | 6709 |
rs781171208 | snp | A/C | 1.65119e-05 | 0.00287327 | missense | SPTAN1 | GRCh38.p7 | 9:128625940 | AACTCAGCCGCCCGC[A/C]AGAAGAAGCTTCTGG | 6709 |
rs781242300 | snp | G/T | 3.31461e-05 | 0.00407086 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128578294 | GATTTTAGCTTATAA[G/T]GCACCAGTTTATCAG | 6709 |
rs781274054 | snp | C/T | 1.67293e-05 | 0.00289212 | downstream-variant-500B, synonymous-codon | SPTAN1, WDR34 | GRCh38.p7 | 9:128633798 | AGCTTCCCGGGGCCC[C/T]TGTTCCGTGAACTCT | 6709 |
rs781277719 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128579520 | CCTAATCTTTCATTT[C/T]GTTTCTCATTTTAGA | 6709 |
rs781287793 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128580742 | GATTAATTAAAACAG[G/T]CCATCCCTTTTATAT | 6709 |
rs781287844 | snp | A/G | 1.65798e-05 | 0.00287917 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128626357 | GCACGTCCAGCCCTG[A/G]CGACTCCGCCAACTC | 6709 |
rs781288268 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571184 | AGCCCCAGCTACTGG[A/G]GAGGCTGAGGTGGGA | 6709 |
rs781297255 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128576513 | AGGGTAGATGAGTAC[A/G]TTGATAAAGTTACCA | 6709 |
rs781309417 | snp | A/C | 1.64743e-05 | 0.00287 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128608088 | CCAAGTGTTTCCTTG[A/C]TGAAGGGCCTCATTT | 6709 |
rs781333852 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128555501 | TGATCCAAAGAAAGG[A/G]GGAAAAAAACCCTGC | 6709 |
rs781343185 | snp | G/T | 2.62836e-05 | 0.00362507 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593062 | GTAGGCTGAGAGTCT[G/T]GCAGAGCACCAATGT | 6709 |
rs781368589 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128566604 | CTTCATTGTTCCTAA[A/G]AAGGGGCTGTCTTCT | 6709 |
rs781381237 | snp | C/T | | | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128612204 | CAACAAGCAGCAGAA[C/T]TTCAACACAGGGATC | 6709 |
rs781428639 | snp | A/G | 1.65748e-05 | 0.00287874 | missense | SPTAN1 | GRCh38.p7 | 9:128585748 | CTACCCATCTTCCAG[A/G]CCATTTTGCTGCAGA | 6709 |
rs781434997 | snp | A/C | 3.06847e-05 | 0.00391681 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592972 | GCTTTTGCTGTGCCC[A/C]CTCTGTGCAGGACAC | 6709 |
rs781437907 | snp | C/T | 1.65012e-05 | 0.00287234 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128584293 | CCAGGACCGAATTGA[C/T]GGCATCACCATTCAG | 6709 |
rs781453058 | snp | C/G | 3.30246e-05 | 0.0040634 | missense | SPTAN1 | GRCh38.p7 | 9:128576896 | GGCAGCGGCTGAAGG[C/G]CCTGGCTCTGCAGAG | 6709 |
rs781467795 | snp | C/T | 1.689e-05 | 0.00290598 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632973 | ATGGGCCTCAGGAGG[C/T]GGGTGAAGAGGTGTC | 6709 |
rs781471335 | snp | A/G | 6.60186e-05 | 0.00574499 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632527 | GGGTGGGGGGTGTTC[A/G]GCAGCAGGGCTGCCT | 6709 |
rs781481694 | snp | A/C/T | 8.4357e-05 | 0.00649405 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618134 | AGAGGCAGGAGCTCC[A/C/T]GGGAACAAGTGGAAG | 6709 |
rs781494631 | snp | C/T | 8.24681e-05 | 0.00642085 | synonymous-codon | SPTAN1 | GRCh38.p7 | 9:128608954 | GGGAGACATTTCTAG[C/T]CGGCGCAATGAGGTC | 6709 |
rs781500513 | in-del | -/A | 0.000132002 | 0.00812304 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128574863 | ACTCAAAGAAAAGGG[-/A]AAGAGACTCCTCTGT | 6709 |
rs781531725 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128571185 | GCCCCAGCTACTGGG[G/T]AGGCTGAGGTGGGAG | 6709 |
rs781542898 | snp | A/G | 1.64727e-05 | 0.00286986 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128581760 | AGGACATTATTCTGA[A/G]CACTTTGTTTCCTTT | 6709 |
rs781551452 | in-del | -/AACAC | 1.65913e-05 | 0.00288017 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582890 | AGCACTCGATTAGTA[-/AACAC]AGCTAAACACAGCTC | 6709 |
rs781560583 | snp | A/G | 1.68352e-05 | 0.00290126 | downstream-variant-500B, synonymous-codon | SPTAN1, WDR34 | GRCh38.p7 | 9:128633882 | CTGAGTCTGCTGGCT[A/G]TTGAACTCCAGACAG | 6709 |
rs781561128 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559532 | CAGGAGCTCGTGTGC[A/G]GTGTCGTTATTGTTC | 6709 |
rs781577911 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128604011 | TCCACGCAGCTGTGA[C/T]TTAGGAAGCAGTTGC | 6709 |
rs781578848 | snp | C/T | 1.64798e-05 | 0.00287047 | missense | SPTAN1 | GRCh38.p7 | 9:128615693 | GCAGTGCCTTCGACA[C/T]CTCCCAAGTAAAGGA | 6709 |
rs781600183 | snp | A/G | 1.68616e-05 | 0.00290353 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128613513 | AGGCGGGCCAGGCCC[A/G]AGTGCCTGGGACACA | 6709 |
rs781612682 | snp | A/T | 1.65151e-05 | 0.00287355 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128605011 | ACTTGGCATTTCTTA[A/T]CCTGAATGTGTCTCG | 6709 |
rs781636957 | snp | A/C | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128592878 | TCCATAGTTTCCCAA[A/C]ATTAAGCATCCACCA | 6709 |
rs781645028 | in-del | -/AA | 3.29457e-05 | 0.00405854 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128618865 | CTTCCTGTCTCCTGT[-/AA]TTAGGGGTCAGCGGC | 6709 |
rs781657651 | snp | C/G | 1.76596e-05 | 0.00297144 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128630133 | CCATCTCTAAAACGG[C/G]AGAAATGCTCCCTGC | 6709 |
rs781678941 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128603061 | CCCTCTGGTAAAGCC[A/G]TTGCCCTTCAACGGG | 6709 |
rs781689993 | snp | C/T | 1.6585e-05 | 0.00287962 | missense | SPTAN1 | GRCh38.p7 | 9:128587696 | CAAGCACAGTCCTGC[C/T]GGGTAAACTTGTAAC | 6709 |
rs781693339 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633488 | TCACTAACCCGCTTC[C/T]GGTCCAGTCACAATC | 6709 |
rs781751951 | snp | A/G | 3.29886e-05 | 0.00406118 | intron-variant | SPTAN1 | GRCh38.p7 | 9:128583982 | CAGGTAGTGTGAACT[A/G]GGGGCTGTGGTTGGG | 6709 |
rs781757667 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128572438 | ACACATCAGCAATGG[A/G]ACAATGGTTCCAGTA | 6709 |
rs794727023 | snp | C/T | | | missense | SPTAN1 | GRCh38.p7 | 9:128580935 | AGCTGACCGTCCTTT[C/T]CGAGGAGAGAGCGGC | 6709 |
rs794727356 | snp | C/T | | | missense | SPTAN1 | GRCh38.p7 | 9:128591603 | GGCAGCATAGCACTG[C/T]GGCAGGAGCAGATTG | 6709 |
rs794727389 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594377 | GACTTCCAGAAGGTA[C/T]GGGCAGTCTTCAGGC | 6709 |
rs794727784 | snp | A/C | | | missense | SPTAN1 | GRCh38.p7 | 9:128576932 | GGAAGCTCTTTGGGG[A/C]AGCAGAAGTTCAGCG | 6709 |
rs794727910 | snp | C/T | | | missense | SPTAN1 | GRCh38.p7 | 9:128577379 | TGTGCTGAGGCTGAC[C/T]GCCTGCAACAGTCCC | 6709 |
rs796053298 | snp | C/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128577205 | TTTGGCCGAGACCTG[C/G]CAAGTGTTCAGGCTC | 6709 |
rs796053299 | snp | A/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128585847 | GTCGGCAGGACCTGG[A/G]GGACTCTCTGCAGGC | 6709 |
rs796053300 | snp | G/T | | | missense | SPTAN1 | GRCh38.p7 | 9:128587684 | GCTTTGCGAGAACAA[G/T]CACAGTCCTGCCGGG | 6709 |
rs796053301 | snp | A/C | | | missense | SPTAN1 | GRCh38.p7 | 9:128587688 | TGCGAGAACAAGCAC[A/C]GTCCTGCCGGGTAAA | 6709 |
rs796053302 | snp | A/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128591588 | CTCCTGGAGGAGCAA[A/G]GCAGCATAGCACTGC | 6709 |
rs796053303 | in-del | -/AG | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128593057 | TGTGAGTAGGCTGAG[-/AG]TCTTGCAGAGCACCA | 6709 |
rs796053304 | snp | C/T | | | missense | SPTAN1 | GRCh38.p7 | 9:128600108 | CCAAGACAGCCTCCC[C/T]GTGGAAGGTAAGAAC | 6709 |
rs796053305 | snp | C/T | | | missense | SPTAN1 | GRCh38.p7 | 9:128600110 | AAGACAGCCTCCCCG[C/T]GGAAGGTAAGAACTC | 6709 |
rs796053306 | snp | G/T | | | missense | SPTAN1 | GRCh38.p7 | 9:128604362 | TCCCTACAGCAGCTG[G/T]CCGAGGAACGGAGCC | 6709 |
rs796053307 | snp | A/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128605398 | AACCAGGCCTGGAGC[A/G]GCCTGGGGAAACGTG | 6709 |
rs796053308 | snp | C/G | | | utr-variant-5-prime | SPTAN1 | GRCh38.p7 | 9:128552666 | CACCCCTCGGCCCGA[C/G]GCACCCACGCCCCTC | 6709 |
rs796053309 | snp | C/T | | | missense | SPTAN1 | GRCh38.p7 | 9:128615833 | GATGACGAGGAGTCC[C/T]GGATCAAGTATGTCT | 6709 |
rs796053310 | snp | A/C | | | missense | SPTAN1 | GRCh38.p7 | 9:128625165 | TCTTCTGTGCAGACG[A/C]TCCTCACCAAACAGG | 6709 |
rs796053311 | snp | C/T | | | missense | SPTAN1 | GRCh38.p7 | 9:128625892 | GAGGCCCGGCACGCC[C/T]CCCTCATGAAGAGGT | 6709 |
rs796053312 | snp | A/C | | | missense | SPTAN1 | GRCh38.p7 | 9:128626527 | TGCGCGAGGCCCACG[A/C]CGCCTTCCGCTCCTC | 6709 |
rs796053313 | in-del | -/CT | | | intron-variant, downstream-variant-500B | SPTAN1, WDR34 | GRCh38.p7 | 9:128633197 | CACCAGGTGCCATCT[-/CT]TACCCCACAGAACCT | 6709 |
rs796053314 | snp | A/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128577461 | ACTGGGAGCAGATCC[A/G]CACCTTGGCGGCAGA | 6709 |
rs796053315 | snp | A/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128582527 | AACAACCACTATGCA[A/G]TGGAAGATGTGGCCA | 6709 |
rs796053316 | snp | A/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128598475 | TCTGAAGGTCTCATG[A/G]CAGAGGAGGTGCAGG | 6709 |
rs796053317 | snp | C/T | | | missense | SPTAN1 | GRCh38.p7 | 9:128608958 | GACATTTCTAGCCGG[C/T]GCAATGAGGTCTTGG | 6709 |
rs796053318 | snp | A/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128609199 | TCCAACAGTTCAGCC[A/G]GGATGTGGATGAGAT | 6709 |
rs796053319 | snp | A/G | | | utr-variant-5-prime | SPTAN1 | GRCh38.p7 | 9:128552696 | CACCCCCCGAGAGCC[A/G]GTGAGAGGGGCAGCC | 6709 |
rs796053320 | snp | A/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128617752 | GCTGCGCATGAGCCG[A/G]CTATTCAGGTAAGGA | 6709 |
rs796053321 | snp | A/C | | | missense | SPTAN1 | GRCh38.p7 | 9:128618934 | TGTGGAAGAGGAAGA[A/C]GCCTGGATCAATGAG | 6709 |
rs796053322 | snp | A/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128626419 | TCCTGACCTTCGCCA[A/G]AAAGGCTTCTGCCTT | 6709 |
rs796053323 | snp | C/T | | | missense | SPTAN1 | GRCh38.p7 | 9:128626535 | GCCCACGACGCCTTC[C/T]GCTCCTCCCTCAGCT | 6709 |
rs796053324 | snp | A/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128626536 | CCCACGACGCCTTCC[A/G]CTCCTCCCTCAGCTC | 6709 |
rs796053325 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128627908 | GTCTCCCGGCTGCTT[A/G]GATCTGCTCTCCACA | 6709 |
rs796053326 | snp | C/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128632158 | TCCGAGCCATGAGAA[C/G]TCAGCTCAAAAAGAT | 6709 |
rs796053327 | snp | A/T | | | missense | SPTAN1 | GRCh38.p7 | 9:128632263 | TCGCCCAGCAGTGGG[A/T]CCAGCTGGACCAGCT | 6709 |
rs796053328 | snp | C/T | | | missense | SPTAN1 | GRCh38.p7 | 9:128632286 | GACCAGCTGGGCATG[C/T]GCATGCAGCACAACC | 6709 |
rs796053329 | snp | C/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128632660 | GACCTGCCCATGGTG[C/G]AGGAAGGGGAACCTG | 6709 |
rs796053330 | snp | C/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128632679 | AAGGGGAACCTGACC[C/G]TGAGTTCGAGGCAAT | 6709 |
rs796053331 | snp | C/T | | | missense | SPTAN1 | GRCh38.p7 | 9:128632703 | AGGCAATCCTGGACA[C/T]GGTGGATCCGAACAG | 6709 |
rs796053332 | in-del | -/CTC | | | cds-indel | SPTAN1 | GRCh38.p7 | 9:128585853 | AGGACCTGGAGGACT[-/CTC]TGCAGGCCCAGCAGT | 6709 |
rs796053333 | multinucleotide-polymorphism | CC/TT | | | missense | SPTAN1 | GRCh38.p7 | 9:128625972 | GGCTCAGAGTCACTT[CC/TT]GCAAGGTGAGGATGG | 6709 |
rs796053334 | in-del | -/CAGCTGGGC | | | cds-indel | SPTAN1 | GRCh38.p7 | 9:128632282 | CTGGACCAGCTGGGC[-/CAGCTGGGC]ATGCGCATGCAGCAC | 6709 |
rs796053335 | in-del | -/GCATGC | | | cds-indel | SPTAN1 | GRCh38.p7 | 9:128632292 | TGGGCATGCGCATGC[-/GCATGC]AGCACAACCTGGAGC | 6709 |
rs796053336 | multinucleotide-polymorphism | AGGT/CGGC | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128632556 | CTGCTGAGCCGCCCT[AGGT/CGGC]TTTGTGCTGCAGACA | 6709 |
rs796053337 | snp | A/C | | | missense | SPTAN1 | GRCh38.p7 | 9:128621233 | AATGATGTCTGCACC[A/C]ATGGACAAGACCTCA | 6709 |
rs796053338 | snp | C/T | | | missense | SPTAN1 | GRCh38.p7 | 9:128632302 | GCATGCAGCACAACC[C/T]GGAGCAGCAGATCCA | 6709 |
rs796053339 | snp | A/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128632583 | GCAGACACTTTGACA[A/G]GGACAAGTCTGGCAG | 6709 |
rs796053340 | in-del | -/ACCAGCTGG | | | cds-indel | SPTAN1 | GRCh38.p7 | 9:128632272 | AGTGGGACCAGCTGG[-/ACCAGCTGG]GCATGCGCATGCAGC | 6709 |
rs796067298 | multinucleotide-polymorphism | CC/TT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128555623 | ATTTGCAAAGCCTTT[CC/TT]TTTTTTTTTTTTTTT | 6709 |
rs796193505 | in-del | -/A | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128620734 | AAAAAGAAAAAAAAA[-/A]GACATGACTTGGAAG | 6709 |
rs796221692 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128616538 | TTGGGAGGCTGAGGC[A/G]GGCAGATCACTTGAG | 6709 |
rs796262635 | snp | G/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128590977 | CAGGCGGCATTGCTC[G/T]TCTGCCTGTGACCCT | 6709 |
rs796307714 | snp | A/G | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128565232 | CACTTGAACCCTGAA[A/G]GCAGAGGGCAGTGAG | 6709 |
rs796349434 | in-del | -/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128559735 | CTTAAATAATTTTGA[-/T]TTTTTTTTTTTTTTG | 6709 |
rs796424572 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128617444 | ACACACAGCAGGGCT[C/T]ATAGATGCATAGATG | 6709 |
rs796473465 | in-del | -/CT | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128594804 | CCATCATGTATGTAG[-/CT]TTTTTTTTTTTTTTT | 6709 |
rs796630862 | snp | C/T | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128586606 | ACATATATACATACC[C/T]ACAAACATACCAGCA | 6709 |
rs796636948 | in-del | -/TTTC | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128589276 | TGTTGGTTCTTTTTT[-/TTTC]TTTTTCTTTTCTTTT | 6709 |
rs796749122 | in-del | -/A | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128582334 | AAGTTATGAGAAAAA[-/A]TGTCATCACCAACCT | 6709 |
rs796792491 | in-del | -/AAAAAAAAAAA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128624102 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAA]GAATTCCTAAAAGTA | 6709 |
rs796930106 | snp | A/G | | | missense | SPTAN1 | GRCh38.p7 | 9:128577428 | AGATTCAAGTGAAGC[A/G]AGAGGAACTGATTAC | 6709 |
rs797046004 | in-del | -/AA | | | intron-variant | SPTAN1 | GRCh38.p7 | 9:128600119 | CCCCGTGGAAGGTAA[-/AA]GAACTCCTTTGCAAA | 6709 |