SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2303761 | snp | C/T | | | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660341 | GGCGCGGGGTGTACG[C/T]GGGCGGGGCCTCCTC | 50855 |
rs3178281 | snp | G/T | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662758 | CTGGGGAACATTAAA[G/T]GTTTTCTACAAATAC | 50855 |
rs3179914 | snp | A/C | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662773 | GGTTTTCTACAAATA[A/C]AGTCATGGTCCTTGT | 50855 |
rs7204371 | snp | A/G | | | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659894 | CCAGAGCCGCGCGGG[A/G]CCTCTCACCAGTCCG | 50855 |
rs8058187 | snp | C/T | 0.095531 | 0.196569 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659534 | GGCGGAGGCATCACT[C/T]ACCAACCAGGCACCC | 50855 |
rs11555862 | snp | C/T | 0 | 0 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661046 | GGAGTCCTCTGCGGC[C/T]GGGCCATGGCGGGGC | 50855 |
rs13331943 | snp | A/T | 0.0043906 | 0.0466478 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659180 | TAAGGTTAAGGCTGG[A/T]GAGATCACTGCACAG | 50855 |
rs28521023 | snp | C/T | 0.20111 | 0.245173 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660685 | TACACAGTGCACGGT[C/T]TTGTAAGGCCAGTGG | 50855 |
rs35356834 | snp | A/G | 0.0615833 | 0.164314 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662462 | GACAGCAGTGACCTG[A/G]TCATTGAGAACCGCC | 50855 |
rs59443695 | snp | A/G | 0.0249278 | 0.108823 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659099 | GGACAGGGGACCATG[A/G]GATGAGTCAAGGCTT | 50855 |
rs61741302 | snp | C/T | 0.00259399 | 0.0359203 | downstream-variant-500B, missense, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663277 | CTCTCAGTGAGTCTG[C/T]CCCAGCAGGCAGCAG | 50855 |
rs72547496 | snp | C/T | 0.0298908 | 0.118541 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660703 | GTGTGTGTGCTCTTA[C/T]TTCCACTGGCCTTAC | 50855 |
rs72547497 | snp | A/C | 0.0102561 | 0.0708723 | upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67660841 | GAAACGGAGCCGTGG[A/C]TGGAGAGGAGCCGTC | 50855 |
rs73597595 | snp | A/G | 0.0031125 | 0.0393264 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660317 | CTCCTTCGCTGGGCG[A/G]GGCCGGAGGAGGAGG | 50855 |
rs75040366 | snp | C/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663030 | TGACTGGGAAGAGTG[C/G]TCTAGGGACACTGGC | 50855 |
rs79241223 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661882 | ATCTCAACATCCCCC[C/T]TCTTCTGCAGCAGAA | 50855 |
rs112282767 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662707 | GCAGGGACTTCACAG[C/T]GGGGGTTTTTAGCTG | 50855 |
rs112600026 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB, missense | PARD6A, ACD | GRCh38.p7 | 16:67661701 | GGGTACAGTGGGCAG[C/T]CTCTGTGGGGTAAGG | 50855 |
rs112770259 | snp | A/G | 0.0119091 | 0.0762411 | upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67660909 | TGCCCCCTTGACGTC[A/G]CGCTCCGGATGGGAA | 50855 |
rs115108685 | snp | C/T | 0.0117731 | 0.0758153 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662443 | TGAGCCTGATAGTGA[C/T]GATGACAGCAGTGAC | 50855 |
rs115805613 | snp | C/G | 0.0225045 | 0.103662 | upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67660912 | CCCCTTGACGTCACG[C/G]TCCGGATGGGAAGGC | 50855 |
rs116715291 | snp | C/T | 0.00201345 | 0.031665 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663144 | TGGAGCTCCTTGCCA[C/T]TGTCCCCCAAAGGGG | 50855 |
rs138202882 | snp | A/T | 0.000153988 | 0.00877328 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662616 | GCTGGGGGAGTCGCA[A/T]TCGAGGAGATGGTAG | 50855 |
rs138527794 | snp | A/G | 0.00497694 | 0.0496357 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660013 | AGGGGCGTGGGATGG[A/G]CCCGCGACCGCGGCC | 50855 |
rs139372052 | snp | C/T | 0.00333756 | 0.0407141 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661580 | ACTTGGCTATACGGA[C/T]GCTCATGGCGACCTG | 50855 |
rs139438549 | snp | C/T | 0.00295464 | 0.0383222 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67658960 | AGGCAGCCCAGTGGG[C/T]GACAGGGGGTGCTGT | 50855 |
rs139574276 | snp | C/G | 0.000181685 | 0.00952939 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662029 | CCAAGATTTCCGCCA[C/G]GTTTCCTCAGTCATA | 50855 |
rs140078781 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661837 | TACAGTGCCCCCTGT[A/G]AACAGCCCAAGTCGG | 50855 |
rs140546833 | snp | A/G | 0.00206004 | 0.0320277 | synonymous-codon, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662515 | GTCTCAGGGGCCCCC[A/G]TGCTGGGACCTGCAC | 50855 |
rs141113896 | snp | C/G | 1.68303e-05 | 0.00290084 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659607 | CCTGGAGATAGAACT[C/G]TGCGGGCTGGAGGAG | 50855 |
rs141258993 | snp | A/G | 0.000396242 | 0.01407 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662236 | TACAGGGCTGCTGGC[A/G]GTCAGTGATGAGATC | 50855 |
rs142115585 | snp | A/G | 3.29516e-05 | 0.00405891 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659257 | GGTGGACTCTGAAAG[A/G]TGCTCCCTACAGGAA | 50855 |
rs142507451 | snp | C/T | 0.00499192 | 0.0497096 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660141 | AGCAGCTGCCCGGCT[C/T]GTGGACTGGAGGGTG | 50855 |
rs142662151 | snp | C/T | 0.000761367 | 0.0194963 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660036 | CCGCGGCCTCGGCGT[C/T]CTGTAGTACCTGACG | 50855 |
rs142762905 | snp | A/G/T | 9.86818e-05 | 0.00702374 | upstream-variant-2KB, missense, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660401 | TGTGTGCAGACTCCC[A/G/T]CTGGTCCACCCCGCT | 50855 |
rs142866742 | snp | C/T | 1.65151e-05 | 0.00287355 | downstream-variant-500B, missense, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663234 | ACCTGCACCAGCTTC[C/T]GGTCCAGCTCAGCAC | 50855 |
rs143279803 | in-del | -/C | | | frameshift-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661635 | TGCACCGGGCCCTGG[-/C]CCAGCGGGCCCCCGC | 50855 |
rs144087853 | snp | A/G | 1.65168e-05 | 0.00287369 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67658992 | CAAGGGCCCTCCAGT[A/G]TCAGGCAGCTTTCAG | 50855 |
rs144160135 | snp | A/C/T | 0.000177925 | 0.00943042 | missense, synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661909 | AGAAGCTGACTCCAG[A/C/T]GGCCTGGCTTTTGCC | 50855 |
rs144415548 | snp | A/C | | | upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67660942 | CGGGGCGTGTGCTAC[A/C]GCCAGGGGCGGGGCG | 50855 |
rs145007645 | snp | A/C/T | 0.00016513 | 0.00908522 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659046 | TGCTCCTGGTCCTCC[A/C/T]GCATTTCATCCAGAA | 50855 |
rs145012859 | snp | C/T | 6.61813e-05 | 0.00575207 | stop-gained, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662375 | CGCAATAACGTGGTG[C/T]GAGGGGCATCTGGGC | 50855 |
rs145510507 | snp | C/G/T | 0.00102335 | 0.0225973 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662154 | GCGTGCGTGTGGCTC[C/G/T]CCAGGGCCTGGAGCG | 50855 |
rs146071407 | snp | A/G | 0.00082434 | 0.0202852 | synonymous-codon, upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67661095 | CATCGTCGAGGTGAA[A/G]AGCAAAGTAAGGGCT | 50855 |
rs146598152 | snp | A/G | 0.00303032 | 0.0388069 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661447 | TCTCCCCCAACCCCG[A/G]CTTCCAGTTTGACGC | 50855 |
rs146699133 | snp | C/T | 5.56798e-05 | 0.00527606 | upstream-variant-2KB, missense, splice-acceptor-variant, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660038 | GCGGCCTCGGCGTCC[C/T]GTAGTACCTGACGGC | 50855 |
rs146942923 | snp | A/C/T | 1.7042e-05 | 0.00291903 | upstream-variant-2KB, synonymous-codon, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659783 | CCCGCGGAAGCCGAA[A/C/T]TCCTTCTCCTCCCTG | 50855 |
rs147566572 | snp | A/G/T | 0.000364127 | 0.0134883 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662388 | TGCGAGGGGCATCTG[A/G/T]GCGTTTGACAGGTCC | 50855 |
rs148124985 | snp | A/G | 5.21698e-05 | 0.00510707 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660240 | ACGGCTACACCCAGC[A/G]GATGCAACGGGCCCG | 50855 |
rs148341217 | snp | A/G | 0.000233528 | 0.0108032 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662493 | AGCCTCCCAGTTCCA[A/G]TGGGCTGTCTCAGGG | 50855 |
rs149051014 | snp | A/C/G | 0.000378888 | 0.0137588 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659240 | GTACCTGCATTGGAC[A/C/G]AGGTGGACTCTGAAA | 50855 |
rs149365469 | snp | C/T | 0.00162346 | 0.0284446 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660199 | TCCAGGGCCGTAGGA[C/T]CAGCCTCCCCGAACC | 50855 |
rs149729712 | snp | A/C/G | 4.95473e-05 | 0.00497711 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662145 | ATGGCATGAGCGTGC[A/C/G]TGTGGCTCCCCAGGG | 50855 |
rs150549185 | snp | A/G | 0.000153988 | 0.00877328 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661941 | CCAACTCTCTGCAGC[A/G]GCGCAAGAAAGGGCT | 50855 |
rs151132164 | snp | A/C/G | 0.000577558 | 0.0169839 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659389 | CTCAAGGCAGTCATA[A/C/G]AGCTTTTTCTGAACA | 50855 |
rs181609307 | snp | A/C | | | upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67660940 | GGCGGGGCGTGTGCT[A/C]CCGCCAGGGGCGGGG | 50855 |
rs184089323 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661156 | TCCCTCTTTCTCCCC[C/T]TCCCAGCTCCTTGGT | 50855 |
rs184418769 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663094 | TGGGATTGGGTCCAA[C/T]CCTGTCCTTTGCAGC | 50855 |
rs185153202 | snp | C/G | | | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661364 | GCTGCCGCAAAAGCG[C/G]CAGCCGCATCTTTCC | 50855 |
rs187837649 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660586 | GGCCGAGTGCCGTCC[A/G]AGCGAGTTGACTCGA | 50855 |
rs187847017 | snp | A/G | 0.00278067 | 0.0371834 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659290 | GAGTGGCCAGGACTC[A/G]GGAACCATGCTGAGG | 50855 |
rs188017607 | snp | C/T | | | synonymous-codon, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662638 | AGATGGTAGTGGCTT[C/T]AGCCTCTGACAGTCA | 50855 |
rs188685722 | snp | C/G | | | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661643 | GGCCCTGGCCAGCGG[C/G]CCCCCGCCACTGCGC | 50855 |
rs189195547 | snp | C/T | 0.000270316 | 0.0116226 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662648 | GGCTTCAGCCTCTGA[C/T]AGTCAGGATGAAGCC | 50855 |
rs192207041 | snp | A/G | 0.0178422 | 0.092751 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662668 | AGGATGAAGCCCCAT[A/G]CCACTCCACACTGCT | 50855 |
rs192803767 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660643 | GAACGGTTCAGCACA[C/G/T]ATTTATTATGACTCA | 50855 |
rs193208247 | snp | A/C/T | 6.66711e-05 | 0.00577331 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659694 | CCCAAGGCAGTCTCA[A/C/T]CACTCACCGCGCCGC | 50855 |
rs199612237 | snp | C/T | 4.04253e-05 | 0.00449566 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660363 | CCCCGCGCCTGCGCA[C/T]GAGGGCGTCCTGCTC | 50855 |
rs199626332 | snp | A/G | 0.0002636 | 0.0114774 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659222 | CACTGGTCAAGCTCT[A/G]CAGTACCTGCATTGG | 50855 |
rs199739793 | snp | A/G | 0.000103075 | 0.00717822 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662556 | GACATCCTGGTACCC[A/G]CAGCTCTCTGCCCTC | 50855 |
rs200163503 | snp | A/G | 4.95593e-05 | 0.00497767 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662127 | TGGGCTTCTACATCC[A/G]AGATGGCATGAGCGT | 50855 |
rs200365807 | snp | C/G/T | 0.000190308 | 0.00975295 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660175 | CTGACCCCAGAATCA[C/G/T]CTCCCGAATCCAGGG | 50855 |
rs200880184 | snp | A/G | 3.30704e-05 | 0.00406622 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662351 | GTCACTGTCAAGCCC[A/G]CCAACCAGCGCAATA | 50855 |
rs200909340 | snp | C/G/T | 8.25258e-05 | 0.00642315 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659387 | CACTCAAGGCAGTCA[C/G/T]AGAGCTTTTTCTGAA | 50855 |
rs201069165 | snp | C/T | 1.65282e-05 | 0.00287469 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662093 | GTGCGGCTGCACAAG[C/T]ATGGTTCAGACCGCC | 50855 |
rs201232409 | snp | C/G | 0.00199797 | 0.0315435 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661045 | GGCCCCGCCATGGCC[C/G]GGCCGCAGAGGACTC | 50855 |
rs201234158 | snp | C/T | 0.000105264 | 0.00725404 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662612 | TCTGGCTGGGGGAGT[C/T]GCATTCGAGGAGATG | 50855 |
rs201635871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661871 | GCAGGTCTCTGATCT[C/T]AACATCCCCCCTCTT | 50855 |
rs201685459 | snp | C/G | 0.000106502 | 0.00729655 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660470 | GTCACTCTGACAGCG[C/G]CCAGGCATTTGGGCC | 50855 |
rs201736719 | snp | C/G | 0.000632953 | 0.0177785 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662484 | AGAACCGCCAGCCTC[C/G]CAGTTCCAATGGGCT | 50855 |
rs201948166 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659617 | GAACTCTGCGGGCTG[A/G]AGGAGTTCGGGGGGA | 50855 |
rs367821436 | snp | A/C/G | 3.29534e-05 | 0.00405904 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659268 | AAAGGTGCTCCCTAC[A/C/G]GGAAGAGAGTGGCCA | 50855 |
rs367827389 | snp | C/T | 1.83646e-05 | 0.00303018 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661869 | GAGCAGGTCTCTGAT[C/T]TCAACATCCCCCCTC | 50855 |
rs367886829 | snp | A/G | 1.65224e-05 | 0.00287418 | downstream-variant-500B, synonymous-codon, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663251 | GTCCAGCTCAGCACG[A/G]TGGCTCTGGGCTCTC | 50855 |
rs368053306 | snp | C/G | | | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661114 | AAAGTAAGGGCTCCT[C/G]CGGCCTCGGCCCTAG | 50855 |
rs368080665 | snp | C/T | 8.26685e-05 | 0.00642864 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662350 | TGTCACTGTCAAGCC[C/T]GCCAACCAGCGCAAT | 50855 |
rs368191589 | snp | A/G | 3.3042e-05 | 0.00406447 | downstream-variant-500B, missense, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663250 | GGTCCAGCTCAGCAC[A/G]GTGGCTCTGGGCTCT | 50855 |
rs368212170 | snp | C/T | 0.000153988 | 0.00877327 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659707 | CACCACTCACCGCGC[C/T]GCCCTCAGCGACCTG | 50855 |
rs368387402 | snp | A/C/G | 7.33777e-05 | 0.00605677 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659970 | TCCCGTCAGACACAA[A/C/G]CAGCGTGGCCCCGAC | 50855 |
rs368510441 | snp | C/T | 5.66963e-05 | 0.005324 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659896 | AGAGCCGCGCGGGGC[C/T]TCTCACCAGTCCGAG | 50855 |
rs368511393 | snp | A/G | 1.77647e-05 | 0.00298027 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67660101 | TCCGCCTCGGTCTCC[A/G]GGCCCTGAATGGGGG | 50855 |
rs368752643 | snp | A/G | 0.000153988 | 0.00877327 | intron-variant, upstream-variant-2KB, missense | PARD6A, ACD | GRCh38.p7 | 16:67661699 | AGGGGTACAGTGGGC[A/G]GCCTCTGTGGGGTAA | 50855 |
rs368882788 | snp | A/G | 1.6534e-05 | 0.00287519 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659090 | TAGGCCTGGGGACAG[A/G]GGACCATGGGATGAG | 50855 |
rs368923570 | snp | A/T | 1.65501e-05 | 0.00287659 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659106 | GGACCATGGGATGAG[A/T]CAAGGCTTAAAGGGG | 50855 |
rs369005864 | snp | A/C/G | 5.14146e-05 | 0.00507002 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663118 | TTGCAGCCATGTGGC[A/C/G]ATCCTCAGCATGGAG | 50855 |
rs369026483 | snp | C/T | 3.37747e-05 | 0.00410928 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661430 | GCTGTCCTGACTCCT[C/T]CTCTCCCCCAACCCC | 50855 |
rs369046068 | snp | C/T | 0.000460348 | 0.0151645 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67660104 | GCCTCGGTCTCCGGG[C/T]CCTGAATGGGGGCTC | 50855 |
rs369086013 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67660830 | CAAGAGCGGAGGACG[A/G]CTCCTCTCCATCCAC | 50855 |
rs369698525 | snp | A/G | 1.92084e-05 | 0.00309901 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660414 | CCGCTGGTCCACCCC[A/G]CTGGTGCACGGGATG | 50855 |
rs369703324 | snp | A/G | | | downstream-variant-500B | PARD6A, ENKD1 | GRCh38.p7 | 16:67662891 | GCAATCAAGCAGCAG[A/G]AGGGCCACCAGGCTT | 50855 |