SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs183693623 | snp | C/G | | | | | GRCh38.p7 | 7:95464812 | TAAATGACTGGTGCA[C/G]AAGTTCTGTGCACCA | 51666 |
rs183701086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95522326 | AATGATGCTCGTGGT[A/G]TTTGAATTACAATAT | 51666 |
rs183724249 | snp | C/T | | | downstream-variant-500B | LOC107986823 | GRCh38.p7 | 7:95474662 | GAGTAGCTGAAACTA[C/T]GGGCACATGCCACCA | 51666 |
rs183730758 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95499996 | CTCCTGCCTCAGCCT[C/G]CCAAGTAGCTGGGAG | 51666 |
rs183732290 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95483289 | ACACGTGGTCTGGCC[A/G]TACTGGTAATTTATG | 51666 |
rs183733535 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539959 | GATTGCTTGCTGCCC[C/T]GCATCTTAAGGCGTA | 51666 |
rs183752611 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASB4 | GRCh38.p7 | 7:95498607 | TAGTCATTTATCAGA[C/T]ACATAGTTTGCACGT | 51666 |
rs183769517 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95459753 | TTTCCTCATCCTCTG[G/T]CTAGAGAAAGCTGAC | 51666 |
rs183853909 | snp | A/G | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:95479112 | AAGCCCTAAAGGCTG[A/G]GGAGTGTGTCTAGTA | 51666 |
rs183896329 | snp | C/T | 0.0763149 | 0.179815 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484955 | TTCTATTTACACACA[C/T]ATATATATATGTGTG | 51666 |
rs184123519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95523332 | TAGCAATTATGATAG[C/T]ATAAGCTTATATCTT | 51666 |
rs184155673 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | ASB4 | GRCh38.p7 | 7:95534073 | TGAATGGCTGGGCGC[A/G]GTGGCTTACACCTGT | 51666 |
rs184195541 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95534497 | CTGATTAGTATTAAG[C/T]CCTATACTTGTTTCT | 51666 |
rs184240566 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95493139 | GTGTCTGGAATCTCA[A/C]AGTAATATATTAGAA | 51666 |
rs184257715 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95506841 | ATTTCCTGGGTGAGT[G/T]CTTTTCTTCTGCTTT | 51666 |
rs184270076 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95528806 | TGTTATAAGCATTTT[G/T]TATGTCTTCATTTAA | 51666 |
rs184277991 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95487218 | CAGGCTAGTTACTAT[G/T]TTTATGATTTTTACT | 51666 |
rs184289266 | snp | C/T | | | | | GRCh38.p7 | 7:95468487 | CAATGGTTTCACAAA[C/T]AAATGTGGACACCTG | 51666 |
rs184310819 | snp | A/C/T | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:95461412 | TGCCCTATTGGATTT[A/C/T]GGACTTGCATGGGAC | 51666 |
rs184384727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95511115 | ATAGGGGAAATGATG[A/G]AAGCTCAGAATTGGA | 51666 |
rs184386600 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | ASB4 | GRCh38.p7 | 7:95488191 | CTAAAAATACAAAAA[A/G]TTAGCCAGGCGCGGT | 51666 |
rs184388461 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95511971 | TGCTGTTTTTGCCTT[A/C/G]TTCTGTGGATCTCAT | 51666 |
rs184404117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472961 | ACTGCTAAATCCTCT[A/G]TTTCCTCTCTCCACG | 51666 |
rs184410580 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95492262 | TCACATAATACACGA[A/G]CAGGATAGAGTCTTT | 51666 |
rs184417197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95516236 | ATATGGTCTGATTTC[A/G]TGAGCCCAACAGATT | 51666 |
rs184512548 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95537190 | TGCTACTTATTGGCT[C/G]TGTTACTTTTAAAAG | 51666 |
rs184528269 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASB4 | GRCh38.p7 | 7:95495643 | GTCATCCCCTCTCCA[C/T]CCCACTTTTATAAAT | 51666 |
rs184530481 | snp | C/T | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469520 | ACAGGAATGAGAAAA[C/T]TTTCCATTTTTTATC | 51666 |
rs184557318 | snp | A/G | 0.00159617 | 0.0282053 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95474023 | TCAGCCTTAACATTC[A/G]ATGAATCTCGATCTT | 51666 |
rs184950073 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASB4 | GRCh38.p7 | 7:95511856 | CAGTGACCTCAATAC[A/G]GAGCTCTCGTTTTGT | 51666 |
rs184962598 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASB4 | GRCh38.p7 | 7:95503044 | AGTATGGACTGTATA[A/G]ATGTATTTTTCTGAA | 51666 |
rs184971592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95494580 | TCAGCCCTAAAGTAA[C/T]TTCTACGCTGTGACT | 51666 |
rs184981458 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ASB4 | GRCh38.p7 | 7:95523866 | TAAGAGTAATATAAA[A/G]GCATTGTTGGTCAGT | 51666 |
rs185064872 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95537889 | AACACTTTACAAACA[C/T]TGCCATTAATCCTAG | 51666 |
rs185074323 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ASB4 | GRCh38.p7 | 7:95492596 | AGCGCTAACATTCTG[C/T]GTTTCTTTGATTTTA | 51666 |
rs185105573 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95517366 | TATGTATTCTAGACA[C/T]GAGTCTTTTATCATA | 51666 |
rs185106918 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95480677 | CTTTTAAAGGGGATT[G/T]TCTAACCCCCGACCT | 51666 |
rs185107626 | snp | A/G | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:95479365 | CAATATGCAAAGTAC[A/G]TTTATATACGTTGTT | 51666 |
rs185111999 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASB4 | GRCh38.p7 | 7:95496705 | CAAAAAAAATTAGCC[A/G]GGCATGGTGGCATGC | 51666 |
rs185115121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95498277 | GGAGTTTGAGTTCAG[C/T]GTGGGCAACATCAGT | 51666 |
rs185203147 | snp | A/C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95522982 | CTCTGCCCACTTAGA[A/C/G]TGAAAACTGCTACAA | 51666 |
rs185223617 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95483939 | TGAGGAAGTATTTCC[A/G]TATATGGCTCTTTTT | 51666 |
rs185349554 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95500664 | GCATATTCTCCTTCT[G/T]CTTTGGTTCACTTGT | 51666 |
rs185351845 | snp | A/G | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:95461970 | TCTCCTTCTGCCATG[A/G]TTATAAGTTTCCTGA | 51666 |
rs185380583 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95506301 | TTCAGACCTGCTCCA[A/G]TGAGTTTCAGGTTGA | 51666 |
rs185386882 | snp | A/C/G | 0.00517822 | 0.0506191 | | | GRCh38.p7 | 7:95466972 | GGGAGCTACAATTCA[A/C/G]GATGAGATTTGGGTG | 51666 |
rs185489033 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95486729 | TGAATTCAGCAAAAC[C/G]AAAAAGTTAACTTTT | 51666 |
rs185629696 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95501195 | TGCCCACTTTACTCT[A/G]CATGAAGCAAATCCT | 51666 |
rs185650131 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484483 | TCAATGTTGATTACA[C/T]GAGTTTGTTCACTAA | 51666 |
rs185668856 | snp | C/G | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:95462354 | GCCCCCTTTGTAATA[C/G]CTTTTTCCTATTTAT | 51666 |
rs185829294 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASB4 | GRCh38.p7 | 7:95535635 | TCTAAATGTTAAAGC[C/T]AAATCTTTCTATCTC | 51666 |
rs185855797 | snp | A/G | 0.00199481 | 0.0315187 | | | GRCh38.p7 | 7:95462730 | AAAAATGTATGCATC[A/G]AGTAGTATTAGCATT | 51666 |
rs185867484 | snp | A/G | 0.00186246 | 0.0304591 | missense | ASB4 | GRCh38.p7 | 7:95528221 | AGGTCACCTCCGTGC[A/G]CCCTGCTGCCCAGCC | 51666 |
rs185942287 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ASB4 | GRCh38.p7 | 7:95514378 | AAACTTACCAAAGCC[C/G]TTTAGCAATAGCTAT | 51666 |
rs185959549 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ASB4 | GRCh38.p7 | 7:95530009 | GAACCAAAGGCCTTC[A/G]TGAAAGATACTTTCT | 51666 |
rs185960430 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95519305 | TAATTCCAGAACATG[C/G]AGAAAATGAAAAGCC | 51666 |
rs185986287 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant, intron-variant | LOC107986823 | GRCh38.p7 | 7:95471108 | TCTGTCCCCTTGGCT[C/T]ATTTCTAAGTGTGTT | 51666 |
rs185988422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95508672 | AGATAATTGGGCTCA[C/T]GCAGGTTTAGGGTCA | 51666 |
rs185993686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95490244 | AGCTCTTATTTCCAC[C/T]CTCTGAATGAATAAT | 51666 |
rs185995291 | snp | C/T | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484732 | AATGCAATTTATTTG[C/T]ATTCTCTTTAGAACT | 51666 |
rs186101699 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ASB4 | GRCh38.p7 | 7:95534894 | TCGTTAAGAGTGTAT[A/T]ATAGCCTCTTCTTGC | 51666 |
rs186107954 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538846 | TCTTTTTATGTAGCA[A/G]ACTGACATTTCATAG | 51666 |
rs186118038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95493955 | GTTGTTTAACCATTC[A/G]AACAATGCTGTAGTG | 51666 |
rs186134857 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ASB4 | GRCh38.p7 | 7:95513022 | TTTAAAATCAGGGAC[A/C]TTTTTTGGCTATAGT | 51666 |
rs186134908 | snp | C/T | 0 | 0 | | | GRCh38.p7 | 7:95475224 | AGGCTGTCAATAGAA[C/T]AGGTAGGGTCATATA | 51666 |
rs186404522 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95498487 | GATTTGCCATCTGTA[C/T]ATTATTTACTTTGGT | 51666 |
rs186406501 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539005 | AGTTAGTGGATTGCA[A/G]AAAGAAAAATGTAGG | 51666 |
rs186414720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95520919 | CTTTTCTTTCCATCT[C/T]ATTCTTTTTTAATTT | 51666 |
rs186423481 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95481447 | AAAGGGATGTCAGAC[C/T]ACTTAATCATCCATT | 51666 |
rs186495673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95513464 | TCTGTTGCCAGAGCC[C/T]TTCCTTGCTTGTGGG | 51666 |
rs186516943 | snp | A/G | 0.0115144 | 0.0749975 | | | GRCh38.p7 | 7:95475531 | TGGGACTACAGGTGC[A/G]TGCCACCACACCTGG | 51666 |
rs186552973 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95476334 | AGCTGTGTGAGGTAG[A/G]TGCGTATTGCATGCT | 51666 |
rs186630255 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538385 | ACATTTGAACCAGAC[A/G]TCACTGAGCCAGAGA | 51666 |
rs186631246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95525733 | TCCATTTCACTCCAG[A/G]GCAAAGACGAGCTGA | 51666 |
rs186670996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95497072 | AGAGGGTAGAGGGGA[A/G]TGTTACAAGATGACA | 51666 |
rs186698133 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95535361 | AGGCATGCCTCTCTT[A/C]TAATGCCTCACCTAA | 51666 |
rs186734281 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95494299 | TCTAGATTTCTTATG[A/G]CCTTATCTAATCAGT | 51666 |
rs186772101 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95524410 | TATTCAAAGTTCAAA[A/T]ATTGGAAAATGGAAG | 51666 |
rs186801218 | snp | C/T | | | | | GRCh38.p7 | 7:95460881 | TCCAGGGCCCCCGTG[C/T]TCTGTGCAGCCTAGA | 51666 |
rs186852578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95518374 | GTGGGGCAAGCCTCA[A/G]GTAGAGATGGCGAAG | 51666 |
rs186886818 | snp | A/C | 0.0103295 | 0.0711199 | | | GRCh38.p7 | 7:95480214 | CTTTTCTTGGTAGCA[A/C]ATATTACCATGTGAC | 51666 |
rs186968879 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ASB4 | GRCh38.p7 | 7:95503401 | AGCTTCTTGGACAGC[C/G]CTTGGCACATAGAAA | 51666 |
rs187001160 | snp | A/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95464910 | AGGTAAGACATTTTA[A/T]GTTTATTGACAACAA | 51666 |
rs187136949 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95530555 | CTAAGGAAAAGCAGG[C/T]GCAAGGGTCCTGAGG | 51666 |
rs187143585 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95521797 | CAAAATAATAGTATA[C/T]TTTTTAAATGGATAC | 51666 |
rs187172064 | snp | C/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95482928 | GGACACTGAGGTTAG[C/T]GGCTCAGCATTAGAG | 51666 |
rs187175477 | snp | G/T | 0.0391387 | 0.134304 | intron-variant | ASB4 | GRCh38.p7 | 7:95499913 | GAGTCTCGCTTTGTC[G/T]CCTGGGCTGGAGTGC | 51666 |
rs187225950 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95511277 | CCACCAAGAAGTGAA[A/C]GCTGCAGGGAAGGCC | 51666 |
rs187243126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95533833 | ACAGTCCCTTGCACA[C/T]AGTAAGTCCTCGAAA | 51666 |
rs187249642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473447 | GCCACAGGTTTATCC[A/G]GGACAATAACAAGCA | 51666 |
rs187257110 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95492411 | GAAGCAGGCTTGGAG[A/G]TAATTCTATTCTGCT | 51666 |
rs187279080 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95525194 | ATTCTCCTCCAAAGT[A/C]TCTGGAAGAAACCAA | 51666 |
rs187308064 | snp | A/G | 0.00755907 | 0.0610114 | upstream-variant-2KB, utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485486 | TGGTTGATTTTACAA[A/G]CTCATATTGCAAAAT | 51666 |
rs187308184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95504596 | GAGTACCACCTGTGC[A/G]ATATGAATTTAATGT | 51666 |
rs187318320 | snp | C/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95466137 | ATTTAATGTCCCCTG[C/T]TTTTTATATAATTCA | 51666 |
rs187368040 | snp | A/G | 0.00318978 | 0.0398085 | | | GRCh38.p7 | 7:95477145 | GCAGCTGTTCTTCCG[A/G]GTTCATTTATCGAGG | 51666 |
rs187393809 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95508334 | AGCTTCCCTTTGAAG[A/G]GCATTTTTTATGTAA | 51666 |
rs187405957 | snp | G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95470512 | AATGAACAAACACTT[G/T]TAGACAGGGCCACTT | 51666 |
rs187489685 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASB4 | GRCh38.p7 | 7:95505615 | TAAGTAGCAATAGAA[A/G]CAGCTTTATGAGAAT | 51666 |
rs187489831 | snp | A/C | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95466811 | TACATGGAGGCAGGC[A/C]AGAGAGCATGGTGCA | 51666 |
rs187596116 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASB4 | GRCh38.p7 | 7:95490559 | GTGTGTAACCTTTGG[C/T]TGTAATAACAGAGGC | 51666 |
rs187646199 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95529759 | AACTGTCCTGTGTTG[A/T]GCTCTAAATAGGTTT | 51666 |
rs187649727 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | ASB4 | GRCh38.p7 | 7:95488774 | AGCTTGATTACTTTT[C/G]ACAAAATAACAAACC | 51666 |
rs187737713 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95514536 | GAGGAAGAGGTTGAC[C/T]GACATGTTCAGTGTC | 51666 |
rs187746935 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95494776 | TGCAGATTTATAGAA[A/T]AAAGACCAGCTCAGC | 51666 |
rs187750349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95536660 | AGAATGCCTTTAAAG[C/T]GTACTCAAATGCAAT | 51666 |
rs187753074 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95467223 | TTATTAATGTTAGAG[A/G]CAGTGGTTTTTGTGG | 51666 |
rs187879335 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95510207 | GTCGATGTTTCTTCC[A/G]AAATGAGTCCCATCA | 51666 |
rs187883431 | snp | G/T | 0.00318978 | 0.0398085 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471390 | AAGGAAAAATGAGGA[G/T]GATCAAGAGTGGTTG | 51666 |
rs187901096 | snp | A/G | 0.000798403 | 0.0199641 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95472023 | AAACATAAGGATCAG[A/G]GGAGGAGTGTGAGTG | 51666 |
rs188102891 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515867 | GCTGCCACTCAAAAA[A/T]GTAGGCTCACTGTTG | 51666 |
rs188114449 | snp | A/G | 0.00358779 | 0.0422022 | | | GRCh38.p7 | 7:95478196 | GCAAATGCTGCCTGG[A/G]GTACAATTGTGAGGT | 51666 |
rs188129360 | snp | C/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95479248 | AGTCTGACGGTCTTT[C/T]ACCATAACACCACTT | 51666 |
rs188133392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95516863 | CATCTGAACTCAAAC[C/T]TGTGTGATCCCATCT | 51666 |
rs188208515 | snp | A/C | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95540067 | TCGCCCAGGGAAATG[A/C]AAACTTTTCTTATTC | 51666 |
rs188217272 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95540225 | ATAAAGCTCTTCTGT[C/T]TCCTTTCATCTTTGT | 51666 |
rs188229512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95498904 | TGTTGAAAAGAATAT[C/T]CTTTCACCATCAAAC | 51666 |
rs188257682 | snp | C/T | 0.00517822 | 0.0506191 | | | GRCh38.p7 | 7:95459882 | AGTTCTCATAATCCC[C/T]ACATGTTGTGGGAGG | 51666 |
rs188368353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95495371 | AACTCTCAATGATTG[A/G]AAGTTTTTTAAAAAA | 51666 |
rs188378370 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95536886 | CCAGAATATTAAAGC[A/G]TTTTGTGTAGATTAT | 51666 |
rs188473900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95523380 | AGTGCAAACAAAGCC[A/G]AACGATTTCACCTAA | 51666 |
rs188504385 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484629 | TCTAAGAATCAAATA[G/T]TATCATTGTAAGTTT | 51666 |
rs188518754 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95462602 | GAGAAGATAATGAAT[A/G]TTTTTCCTGTGACCT | 51666 |
rs188525972 | snp | A/C | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95481607 | AAGTGATTGTGGCTT[A/C]GTAGCATCAAATTCA | 51666 |
rs188534524 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95521465 | TTTAAACTCTACTGA[A/T]GGACATATACATTGA | 51666 |
rs188626144 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95506975 | TTATTCTCTACTTGC[C/T]GGGAGATCTTTTCTA | 51666 |
rs188641924 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ASB4 | GRCh38.p7 | 7:95529142 | TTTAATATGCTGTGG[C/T]AAATGACAAGGTAGA | 51666 |
rs188645987 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95468869 | TGACAGTTCAATTTA[A/G]TCTTTTGTTGCTTTG | 51666 |
rs188652881 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95487225 | GTTACTATGTTTATG[A/T]TTTTTACTCAAGGGC | 51666 |
rs188726133 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ASB4 | GRCh38.p7 | 7:95528651 | CATCTTTTAAACAGA[A/C]TGACTGATCTAAAGA | 51666 |
rs188754957 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ASB4 | GRCh38.p7 | 7:95486832 | GGAAAACAAAAATTA[A/G]ACCAATTTTTTTTTA | 51666 |
rs188883551 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95510869 | TGAAGTTTCCTTAGG[A/C]CTGTACTTCTTTATT | 51666 |
rs188889220 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95513142 | GGAGGCCATGGTCAC[A/G]AAATGTGGGAAGCCT | 51666 |
rs188974705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95507411 | CTTCTACTCCTGTGC[A/G]AAGTCTTAGTTCAGA | 51666 |
rs188981125 | snp | C/G/T | 0.000300157 | 0.0122471 | missense, intron-variant | ASB4 | GRCh38.p7 | 7:95537595 | GATTTTTACCACTCT[C/G/T]TCTTTACTGTGTGCT | 51666 |
rs189001920 | snp | A/T | 0.0513262 | 0.151752 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95470427 | CTTTTATGCTTTTTT[A/T]AAAAAAAACTCTTAA | 51666 |
rs189017407 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95506576 | TAGCATGGTGAAGGC[A/T]TTGCCCCATTGCCTT | 51666 |
rs189158839 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95532108 | AGATGCTTCAAAGTG[A/G]TTTAGAACAACTACT | 51666 |
rs189188677 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95492052 | TTCAGCTCCCCAGAG[A/G]CAGCAGCTAAGGTGT | 51666 |
rs189247483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95534967 | TGCTGCCAGCTGGCT[C/T]CATCTTACCAGCTCT | 51666 |
rs189272957 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASB4 | GRCh38.p7 | 7:95488294 | TGCAGTGAGCCCAGA[C/T]GGCGCCACTGCACTC | 51666 |
rs189273154 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95529554 | ACTTTCAAATGAAGA[A/T]TTGATGGGTTCAGCA | 51666 |
rs189393227 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95537902 | CACTGCCATTAATCC[C/T]AGAATATCATGGTAT | 51666 |
rs189404092 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95517737 | TGAGCAGTTCCAGTG[C/G]AGTGTGGGGACAGAG | 51666 |
rs189437084 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95496898 | CAAATGGGAAGGAGA[C/T]AGCCATTAAAAAAGA | 51666 |
rs189527307 | snp | A/G | 0.00676609 | 0.0577691 | | | GRCh38.p7 | 7:95480688 | GATTGTCTAACCCCC[A/G]ACCTTTGTGTCTTTA | 51666 |
rs189537239 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95492635 | TGGTGTTTTCTTAAT[C/T]AGCTCTCTGCTGCTT | 51666 |
rs189539164 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95534106 | TCCCAGCACTTTCAG[A/G]TGCCTAGGCGGGCGG | 51666 |
rs189549903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95522360 | ACACCTCTATCAGTT[C/T]GAATATGTAGCTGTT | 51666 |
rs189552049 | snp | A/T | 0.0182019 | 0.0936463 | downstream-variant-500B | LOC107986823 | GRCh38.p7 | 7:95474701 | TAATTTAAAAAAAAA[A/T]TTTTTTTAGAGATGG | 51666 |
rs189560176 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95493827 | GTAATATATCTTGAG[A/C]TCTTTCCATTTCAGT | 51666 |
rs189581260 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95500036 | TTTTAAGAAGCGGGA[C/G]AAAGTAAAAGATGGT | 51666 |
rs189641294 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95518701 | AGTCCAACAAGATGA[C/T]GTACAAATCTTTAAC | 51666 |
rs189658740 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95480431 | AAAATCCTCTCTCAC[C/T]CTGAATCAGTGCTAG | 51666 |
rs189819700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95511887 | CCACTAGGTGGTGCT[A/G]CCTTCCCTTTGCTAC | 51666 |
rs189829208 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95500971 | TTTCTATGTGTAGCC[A/G]TCACCACTCTTCACA | 51666 |
rs189829361 | snp | A/G | 0.00557542 | 0.0525036 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95474084 | TTTGCTAAAAGTTGG[A/G]GCGCACCCTTACTTG | 51666 |
rs189833003 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95461993 | TTTCCTGAGGCCTCC[C/T]GTGCCATGTGGAACT | 51666 |
rs189887706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95519536 | TGTTTTGTACTGAGG[C/T]AGGTGCAGGTCAAGG | 51666 |
rs189898348 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASB4 | GRCh38.p7 | 7:95498289 | CAGCGTGGGCAACAT[C/T]AGTTTGCAATCATTA | 51666 |
rs189908200 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538848 | TTTTTATGTAGCAGA[C/T]TGACATTTCATAGCA | 51666 |
rs189916177 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538566 | AGTTGTGTTTCTGAC[A/G]TGAAGTGTGATTTTT | 51666 |
rs189937108 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95498043 | TTATATAAATACCTA[G/T]GAGTGGGATGATGGC | 51666 |
rs190045767 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95522996 | AATGAAAACTGCTAC[A/G]AATTTTATAGGGTAT | 51666 |
rs190071570 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484121 | TCGCTTAAACTTAGG[A/T]GTCGGAGATCAGCCG | 51666 |
rs190133105 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASB4 | GRCh38.p7 | 7:95525217 | GAAACCAACCCTAGA[C/T]ACTTTAATTTTGGAC | 51666 |
rs190166421 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95504947 | GTAAAGCATGTTCCA[C/T]GAAAAATCATACCAC | 51666 |
rs190168232 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485693 | AAATAATTGTGACAT[A/T]TCATGCCTGGAAATG | 51666 |
rs190277901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95530293 | AACACGGTGAAACCC[C/T]GTCTCTAATAAAATA | 51666 |
rs190307452 | snp | A/T | 0.00119737 | 0.0244387 | nc-transcript-variant, intron-variant | LOC107986823 | GRCh38.p7 | 7:95471115 | CCTTGGCTCATTTCT[A/T]AGTGTGTTTTCTAAT | 51666 |
rs190309581 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95508752 | GTTCCAGCAAAAGAG[A/T]TATTAAAATGATAAA | 51666 |
rs190318177 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ASB4 | GRCh38.p7 | 7:95490366 | AAACTTTTTTCTTTT[A/C]CATTTTACACTTCAA | 51666 |
rs190449061 | snp | C/T | | | | | GRCh38.p7 | 7:95465166 | AAATATGACTTTATA[C/T]CTAGCATTTCAACAT | 51666 |
rs190461059 | snp | C/G | 0.00398564 | 0.0444627 | | | GRCh38.p7 | 7:95475357 | TATTGGCAGTGGTCA[C/G]TGACTCCCCATTGCA | 51666 |
rs190465956 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95494041 | CATTTCACAGAGTAC[A/C]ATGCAAATGTTGTTT | 51666 |
rs190479585 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95512440 | TGTTGTCTAGAAATG[C/T]GTTTCCCAAAGTCCA | 51666 |
rs190508720 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95483793 | CAAATGGTAGATACT[C/T]GATGGGTATTTGTGG | 51666 |
rs190605864 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95479946 | TCTGCTGCTCCCATG[A/G]CCTAGAAATCTCTTT | 51666 |
rs190697470 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95534785 | TAAAGACAAAAAACA[G/T]GTCATAAATCTCCCA | 51666 |
rs190751224 | snp | C/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95461513 | ATTGTATCTAGGAAG[C/T]AACTAACTTGCTTTT | 51666 |
rs190811092 | snp | G/T | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539499 | AATTATTCACATAAA[G/T]CTTGATCTTTCAAAA | 51666 |
rs190817427 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95520983 | CTTTTCCAAAATTGA[C/T]TTATTTTTGCTCTTT | 51666 |
rs190921220 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95514447 | GGTGAAATTTCTATT[A/C]ATTACATCATAAAAA | 51666 |
rs190933174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95536084 | TTTTTCACTTGCTCG[G/T]GGAAGGTGAAAGAAA | 51666 |
rs190940664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95510360 | ATTTGCTCCAACAAG[A/G]GTGTAGATAAGTGAT | 51666 |
rs190941240 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95476563 | CCAGGGCTGGGAAAC[G/T]GGAACAATATCTTTG | 51666 |
rs190956399 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95494598 | CTACGCTGTGACTGT[G/T]GAAGAACTATCTCTT | 51666 |
rs190961905 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASB4 | GRCh38.p7 | 7:95523983 | TAAAATTAAATAGAC[A/G]GAAAATACCAATGTT | 51666 |
rs190977521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471525 | GTTTACACCTATTAG[C/T]AATTATATTTGTATG | 51666 |
rs190979154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95488904 | CAATGCACAAAACCT[A/G]TAACGAATCTCATGC | 51666 |
rs190998401 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95470553 | TGTGCAATAAAAGTA[C/T]ATTTTTATCAATAAA | 51666 |
rs191081700 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95535392 | CACCAAGTGAAAGGG[A/G]CTTTAGGAGGACCCC | 51666 |
rs191123043 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95494337 | ACAATGTTTACTTCT[C/T]TTGTTCTGGACACTA | 51666 |
rs191181783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95531032 | GAATGAGTATACCCT[A/G]AATTTATGCCTTGGC | 51666 |
rs191205949 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95490822 | CACACACGCGCACGC[A/G/T]TGCACACACACACGA | 51666 |
rs191334386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95513652 | AATAGCTAAGCAGCA[C/T]GGCCCAGCCAAGTTG | 51666 |
rs191370738 | snp | A/G | 0.00159617 | 0.0282053 | | | GRCh38.p7 | 7:95476058 | ATCTTTCCTTTTTAT[A/G]ATGCCAGCTCCCTGT | 51666 |
rs191411461 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95537841 | CTAAATAAAATGGTA[C/T]TTGGGTTGATTATAA | 51666 |
rs191432586 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95540102 | TGCTTGTGCTTAAAC[A/T]CTTATGTTCATCTAG | 51666 |
rs191551498 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ASB4 | GRCh38.p7 | 7:95540234 | TTCTGTCTCCTTTCA[C/T]CTTTGTGTTTACTTA | 51666 |
rs191587374 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95521948 | TTTTCTGTAAAACTC[A/G]TAGGACAGAAGAAAA | 51666 |
rs191592363 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95483114 | TCAGAATCACACACT[C/G]TAGTAGCCAGATAGG | 51666 |
rs191593948 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASB4 | GRCh38.p7 | 7:95499942 | GCAGTGGTGCGATCT[C/T]GGCTCACTGCAAGCT | 51666 |
rs191605720 | snp | A/C | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95461115 | GGTGGAGACCCCTCA[A/C]AGAGTCCCCACTGGG | 51666 |
rs191682386 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ASB4 | GRCh38.p7 | 7:95511350 | TTCTTTGTTTTCTTG[A/C]GGCCTCAGAATTCTG | 51666 |
rs191694848 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95492595 | CAGCGCTAACATTCT[A/G]TGTTTCTTTGATTTT | 51666 |
rs191701909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95533892 | TCTCTCGTGCCTATT[A/G]GGATTTCTGAAGCTG | 51666 |
rs191704887 | snp | A/G | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:95466559 | TATGGTTGTGCAAAG[A/G]AAGACATTTTTATCT | 51666 |
rs191784830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95503504 | GGGACCCACTGCCAC[C/T]TAATAAATGAAAACT | 51666 |
rs191829070 | snp | A/G | 0.00438332 | 0.0466095 | | | GRCh38.p7 | 7:95460242 | CCTCAAAATGTGAAA[A/G]CAACTTTGGAACTGG | 51666 |
rs191888260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95498595 | TATTCCGAATACTAG[C/T]CATTTATCAGATACA | 51666 |
rs191915990 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95529779 | TAAATAGGTTTTATA[C/T]AGACTATTTCATTTT | 51666 |
rs192034404 | snp | C/T | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484762 | TTGCTATTATAATTT[C/T]CCTAATTTTTAATGA | 51666 |
rs192075576 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ASB4 | GRCh38.p7 | 7:95524513 | TAAAAAAAACTGTAC[A/G]TATATATTTTATATA | 51666 |
rs192220179 | snp | G/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95481477 | TTCTGTAATAGCAAG[G/T]ACATCTAATTCAGCT | 51666 |
rs192235142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95506758 | GGTAGGTTTATCTTC[A/G]TCCTTTGTACTGAGT | 51666 |
rs192236054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95508530 | GAAACACTGGGTTTC[C/T]GAGCAGTCTGGAGGG | 51666 |
rs192249837 | snp | C/T | 0.187685 | 0.242109 | intron-variant | ASB4 | GRCh38.p7 | 7:95515340 | CTTCCTTCCTTTCTT[C/T]CTTTCTTTCTTTTTC | 51666 |
rs192255191 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95486966 | GTTAGATCATCTGGC[A/G]AGCATACTGCAAACA | 51666 |
rs192257229 | snp | A/C/T | 0.00199529 | 0.0315338 | intron-variant | ASB4 | GRCh38.p7 | 7:95495174 | GAGTTGCCTTAAATT[A/C/T]GTCTTTGGAAAGCGA | 51666 |
rs192265538 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASB4 | GRCh38.p7 | 7:95536797 | AAGTATATAAAGGTG[C/G]CAGTTTTCCTTTCTT | 51666 |
rs192351191 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASB4 | GRCh38.p7 | 7:95503091 | GCATATCAAAATAAT[A/G]TTTAAAATATCAGAG | 51666 |
rs192377556 | snp | C/T | 0.00318978 | 0.0398085 | | | GRCh38.p7 | 7:95463282 | AAGTGACCCTCCTGC[C/T]TCTGCTTCCCAAAGT | 51666 |
rs192377968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95511097 | AACCAAGAAAACATA[C/T]AAATAGGGGAAATGA | 51666 |
rs192398345 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472782 | CTAGCCCCAAGGAGC[A/C]CTCCTCAGGAGCAAC | 51666 |
rs192406233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95492087 | TTACCACCTACCTAC[A/G]CACATTCCTATCTTA | 51666 |
rs192529920 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95517043 | GTCCAGAAAGAAAGT[A/G]TTTCCTATCCCTGTG | 51666 |
rs192531525 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95479306 | TCTATTAGTCCACTG[A/G]TATGAACAACAGTAA | 51666 |
rs192538663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95496347 | AGTCAATGAAAAAGA[A/G]AAAATACTCCTGCCC | 51666 |
rs192579940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95537053 | ACCAGTCCTTCCCAC[C/T]GAACACCCTTGGTTC | 51666 |
rs192600962 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ASB4 | GRCh38.p7 | 7:95495380 | TGATTGAAAGTTTTT[A/T]AAAAAAATATCCTTG | 51666 |
rs192729764 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95481728 | TGGGACTTTGTGCCT[A/G]CTGTCTCAGCCATGG | 51666 |
rs192730089 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95521707 | AAAAAAAACAGTTCT[C/G]TATTCAAAGACATGT | 51666 |
rs192784779 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95534227 | GCATGATTTGTAATC[C/T]CAGCTACTTGGGAGG | 51666 |
rs192860729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95516214 | AAAACACCTTTCTGA[C/T]CATAATATATGGTCT | 51666 |
rs192869060 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95478574 | TAGCATCGTGCCAGC[C/G]ACCAAGATTCTCCGG | 51666 |
rs192926278 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95499794 | ACAGCTGAAGATGCA[C/T]GAGACAGGATAACTG | 51666 |
rs192928283 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473574 | TTGGTCTCCCTTGCT[C/T]TTGCAACCTGAAAGA | 51666 |
rs192993155 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95477668 | GCAATTTTGTGCAAA[C/T]ATGTAAGTGAGATGG | 51666 |
rs193046016 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95461710 | GAATGATATGGTTTG[G/T]TTGTGTCCCCACTCA | 51666 |
rs193047817 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95500039 | TAAGAAGCGGGACAA[A/G]GTAAAAGATGGTTTT | 51666 |
rs193051414 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95532346 | ATTACATAAGCGGGG[G/T]AAAAAAGAATTATAG | 51666 |
rs193098028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95526426 | CCCTTCTCTGCTGTG[C/T]TGCCGGTTGCAACTT | 51666 |
rs193104226 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95486366 | TCTCTCCTTTTCTTT[G/T]CCCACCCTTGGGCCT | 51666 |
rs193186184 | snp | C/T | | | intron-variant, utr-variant-3-prime | ASB4 | GRCh38.p7 | 7:95528740 | TTTAATGAAAGCTAA[C/T]GTTTATTAAGTACTA | 51666 |
rs193218085 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95522638 | CTTATCTGTGTTGGT[C/G]CTCCCGTTTAGTACC | 51666 |
rs193228845 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95483821 | TGGAAAGAATCATAA[C/T]AATAGCATAAAACAG | 51666 |
rs193263491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95506256 | GTATTTTATCAATGT[C/T]ATTTTCTTGAAAAAG | 51666 |
rs193263638 | snp | A/G | 0.00279162 | 0.0372561 | | | GRCh38.p7 | 7:95466815 | TGGAGGCAGGCAAGA[A/G]AGCATGGTGCAGGGG | 51666 |
rs199517534 | snp | C/T | 3.31362e-05 | 0.00407026 | missense | ASB4 | GRCh38.p7 | 7:95536518 | AGATGGAACACAAAG[C/T]GGAGAAGAGCTATCC | 51666 |
rs199528876 | in-del | -/GTGTGT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95493362 | AAAAAAGAGATGAAA[-/GTGTGT]GTGTGTGTGTGTGTG | 51666 |
rs199548926 | in-del | -/A | | | intron-variant | ASB4 | GRCh38.p7 | 7:95504349 | ACAGTGACACAAGTC[-/A]ACCACATGTTAGGAA | 51666 |
rs199549666 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95534274 | CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAG | 51666 |
rs199567239 | in-del | -/TGTG | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484984 | GTATATATGTATATA[-/TGTG]TGTGTATATATGTAT | 51666 |
rs199595000 | in-del | -/TTTC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515365 | TTTTTCTTTCTTTCT[-/TTTC]TTTCTTTCTTTTCTT | 51666 |
rs199663510 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95518195 | CTCTTCCACTCCAGG[C/T]TCATGGAAGACCACG | 51666 |
rs199681056 | snp | C/T | 0.289683 | 0.24683 | intron-variant | ASB4 | GRCh38.p7 | 7:95502389 | AAATAGGTACCAGCC[C/T]GCGGGGGGGGGGCAA | 51666 |
rs199762204 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95530103 | ATGGAGAAAAAGCAG[A/G]GCAAAAAAAAAAAAA | 51666 |
rs199960620 | in-del | -/A | | | | | GRCh38.p7 | 7:95476397 | TTCTTTTTTATATTT[-/A]AAAAAAAAATTTATA | 51666 |
rs200028108 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515167 | TCTTTCTTTCTCTTT[C/T]TCTTTCTTTCTTTCT | 51666 |
rs200166210 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515308 | CTTTCTTTCTTTCTT[C/T]CTTTCTTTCTTCCTT | 51666 |
rs200197495 | in-del | -/TGTG | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513294 | ATCGAGCCAATAGAA[-/TGTG]TGTGTGTGTGTGTGT | 51666 |
rs200204859 | in-del | -/AG | 0.02016 | 0.0983543 | intron-variant | ASB4 | GRCh38.p7 | 7:95502116 | ACAACTAAAAAAAAA[-/AG]AGAGAGAAAGAGGTA | 51666 |
rs200311462 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95527898 | CCTTTCGGAGCTGGT[A/G]GCCTTCTACGTGGAA | 51666 |
rs200333444 | in-del | -/AGT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95518708 | AAGATGATGTACAAA[-/AGT]TCTTTAACAGGGATT | 51666 |
rs200367853 | snp | A/G | | | | | GRCh38.p7 | 7:95481359 | AAGAATAGCAAAAAA[A/G]GGAAAAAAAAACAAC | 51666 |
rs200445929 | in-del | -/T | 0.0126979 | 0.078662 | intron-variant | ASB4 | GRCh38.p7 | 7:95516340 | AATTTTAATCAATGG[-/T]TTTTTTGGAATTAAA | 51666 |
rs200451840 | in-del | -/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95529634 | AAGATTAACTAATTC[-/T]TTTTTTAAAAAATTA | 51666 |
rs200479854 | in-del | -/AAT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95522404 | TGGGCTTAAGCAAAT[-/AAT]ATTTCATTATATCAT | 51666 |
rs200592595 | in-del | -/A | | | intron-variant | ASB4 | GRCh38.p7 | 7:95521699 | TTAAAAAAAAAAAAA[-/A]CAGTTCTCTATTCAA | 51666 |
rs200684162 | in-del | -/TATA | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484989 | ATATGTATATATGTG[-/TATA]TATGTATATATGTGT | 51666 |
rs200738090 | snp | G/T | 0.289683 | 0.24683 | intron-variant | ASB4 | GRCh38.p7 | 7:95502390 | AATAGGTACCAGCCT[G/T]CGGGGGGGGGGCAAA | 51666 |
rs200753139 | snp | A/G | | | | | GRCh38.p7 | 7:95465655 | CAGGCACATGCCACT[A/G]TGCCTGGCTAATTTT | 51666 |
rs200791137 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95518557 | AATTAAGTTTATTCT[A/G]ACTAAATCCTAACCT | 51666 |
rs200806128 | in-del | -/AACT | 0.0142736 | 0.0832652 | intron-variant | ASB4 | GRCh38.p7 | 7:95487404 | AATGTCTGAATGCTA[-/AACT]AATTTTTAAGATGTT | 51666 |
rs200892706 | snp | C/G | 0.000264774 | 0.0115029 | missense | ASB4 | GRCh38.p7 | 7:95495764 | TTTTTTCAGGTTACT[C/G]GTTGCCTAGCTATAA | 51666 |
rs200922744 | in-del | -/AT | | | | | GRCh38.p7 | 7:95462236 | TTCTCTGTGATATAA[-/AT]ATATATATATTTTTG | 51666 |
rs200972163 | in-del | -/TGTGTG | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513294 | ATCGAGCCAATAGAA[-/TGTGTG]TGTGTGTGTGTGTGT | 51666 |
rs200976599 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95502116 | ACAACTAAAAAAAAA[A/G]GAGAGAGAAAGAGGT | 51666 |
rs200980319 | in-del | -/A | 0.0252325 | 0.109451 | intron-variant | ASB4 | GRCh38.p7 | 7:95535704 | TATTTTTGGTTGGTT[-/A]ATAAACTATTAAACA | 51666 |
rs200981404 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95490552 | GAGCAGTGTGTGTAA[A/C/T]CTTTGGCTGTAATAA | 51666 |
rs201031563 | in-del | -/AT | 0.0528381 | 0.153711 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484953 | TTTCTATTTACACAC[-/AT]ACATATATATATGTG | 51666 |
rs201104760 | snp | C/T | 0.000165451 | 0.00909384 | missense, intron-variant | ASB4 | GRCh38.p7 | 7:95537728 | CATTGAAAAAGTACT[C/T]GCTTTTAGAGCCAGA | 51666 |
rs201119405 | snp | C/T | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484957 | CTATTTACACACACA[C/T]ATATATATGTGTGTA | 51666 |
rs201127545 | in-del | -/T | 0.486266 | 0.0817214 | intron-variant | ASB4 | GRCh38.p7 | 7:95506687 | GGGGAATTTAGATTC[-/T]TTTTTTTTTTTTTTT | 51666 |
rs201242200 | in-del | -/AAAT | | | | | GRCh38.p7 | 7:95467040 | TTTTCTAGAACCACA[-/AAAT]AAATAATGATTTTTT | 51666 |
rs201243855 | in-del | -/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95502386 | GTAAATAGGTACCAG[-/C]CCTGCGGGGGGGGGG | 51666 |
rs201275152 | snp | C/G | 1.64765e-05 | 0.00287019 | missense | ASB4 | GRCh38.p7 | 7:95486086 | AAGGCTATTTTGATC[C/G]AAAGGCAAATAGATG | 51666 |
rs201286478 | in-del | -/CTC | 0.00557542 | 0.0525036 | | | GRCh38.p7 | 7:95479332 | AGTAATAATATGTAA[-/CTC]TCCTATAATGCTTCA | 51666 |
rs201545170 | in-del | -/TGTGTATATATGTATATA | 0.0134861 | 0.0810011 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484967 | ACACATATATATATG[-/TGTGTATATATGTATATA]TGTGTATATATGTAT | 51666 |
rs201556151 | snp | A/G | 6.5975e-05 | 0.0057431 | missense | ASB4 | GRCh38.p7 | 7:95528008 | AGGAGCAGGAGTACA[A/G]CACGGAGCACCACCT | 51666 |
rs201560464 | snp | G/T | | | downstream-variant-500B | LOC107986823 | GRCh38.p7 | 7:95474971 | AGGAGGGATTCAGGA[G/T]ATACTTTTGCAATAT | 51666 |
rs201590732 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95488346 | ACTCCGTCTCAAAAA[A/G]AAAAAAAAAAAGAAG | 51666 |
rs201716402 | in-del | -/CGGTGGC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95534071 | ATGAATGGCTGGGCG[-/CGGTGGC]CGGTGGCTTACACCT | 51666 |
rs201717744 | in-del | -/T | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95470421 | TAGGAACTTTTATGC[-/T]TTTTTTAAAAAAAAC | 51666 |
rs201770734 | in-del | -/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95510858 | AAATTGAAGGATGAA[-/G]TTTCCTTAGGCCTGT | 51666 |
rs201781804 | in-del | -/A | 0.00755907 | 0.0610114 | intron-variant | ASB4 | GRCh38.p7 | 7:95488446 | AGGAATGGAAATGAC[-/A]AATAGAATCCTAGCT | 51666 |
rs201880296 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95493386 | TGTGTGTGTGTGTGT[A/G]TGTGTATGTGTGTGT | 51666 |
rs201931788 | in-del | -/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515424 | CTCTCTTTTTTTTTT[-/T]AAGACAGAGTCTCAT | 51666 |
rs201999530 | snp | A/G | 1.8479e-05 | 0.0030396 | intron-variant | ASB4 | GRCh38.p7 | 7:95536585 | CTAATAGTTTTCACT[A/G]TCAAGTACTTCCAGA | 51666 |
rs202006482 | in-del | -/ATC | 0.0667028 | 0.170006 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484126 | AAACTTAGGAGTCGG[-/ATC]AGATCAGCCGGGGGA | 51666 |
rs202069739 | in-del | -/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515425 | CCTTTCTCTCTCTCT[-/C]TTTTTTTTTAAGACA | 51666 |
rs202149475 | snp | A/G | | | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95473890 | ACTCACTGGCTGTGG[A/G]GTTAGGTCAGAAGGG | 51666 |
rs202221772 | snp | A/G | 4.94597e-05 | 0.00497266 | missense | ASB4 | GRCh38.p7 | 7:95495971 | GTGGGGCAAAGCTCA[A/G]TTGCTACTCCTTAAG | 51666 |
rs207468303 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95517913 | AGTATGCTTAGAAAA[C/T]GAGGGCAAAGAGTCC | 51666 |
rs267601648 | snp | C/T | | | missense, intron-variant | ASB4 | GRCh38.p7 | 7:95537691 | TGCCATAGAGCAATT[C/T]CTTTGCTTTCCCTCC | 51666 |
rs267601649 | snp | C/T | | | missense, intron-variant | ASB4 | GRCh38.p7 | 7:95537707 | CTTTGCTTTCCCTCC[C/T]ATTGTCATTGAAAAA | 51666 |
rs367544749 | snp | C/G | 4.94637e-05 | 0.00497287 | missense | ASB4 | GRCh38.p7 | 7:95528089 | ACGACTTTAAATCTC[C/G]CCTCCACAAGGCAGC | 51666 |
rs367594192 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95520758 | CACTGCCACACCTGT[C/G]ATTACAGATGCTTTC | 51666 |
rs367602513 | in-del | -/TTTC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515232 | CTTTCTTTCTTTCTT[-/TTTC]TTTCTTTCTTTCTTT | 51666 |
rs367605593 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95529265 | TGAAAATAAATCAAA[C/T]AATACTATACTTAGG | 51666 |
rs367607454 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95500160 | AAAAATGAGAGGAGA[C/G]CAGAAAGCATAGACA | 51666 |
rs367716657 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95517835 | TTTCAAGGAGTTCAA[A/G]CAAAAAGCAATAGAA | 51666 |
rs367792654 | snp | G/T | | | | | GRCh38.p7 | 7:95463435 | ATGTCATGTCCAGTT[G/T]TAATCCCCAATGTTG | 51666 |
rs367808314 | in-del | -/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95506686 | TGGGGAATTTAGATT[-/C]TTTTTTTTTTTTTTT | 51666 |
rs367888288 | snp | C/T | | | | | GRCh38.p7 | 7:95481553 | TCTAGTTTCCAATTC[C/T]AGCTGGCTTCAAATT | 51666 |
rs367947916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95523982 | CTAAAATTAAATAGA[C/T]GGAAAATACCAATGT | 51666 |
rs367995356 | in-del | A/GGCCATATG | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472232 | CATTCTTTCCCCAAA[A/GGCCATATG]ATGTGTCCAAAATTG | 51666 |
rs368004682 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95511195 | AAGCTAATGGGGACA[G/T]AATAACGGTGGACCC | 51666 |
rs368018093 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95489789 | GATATAACATTAATT[A/G]TGAGCCAACCACTGA | 51666 |
rs368032394 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95504426 | GCCTTCATTTTAATC[C/T]GAAATAGATATGCCT | 51666 |
rs368213573 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95524597 | CACACACACACAAAG[A/T]TACGTTCAAGTTCCA | 51666 |
rs368236107 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515690 | AAAGTGCTGGGACTA[C/T]AGGCGTGAGCCACTG | 51666 |
rs368285522 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95534170 | ACCAACATGGTGAAA[A/C]CTCGTCTCTGCTAAA | 51666 |
rs368375362 | snp | C/T | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539418 | AGTTTTACTCAGATA[C/T]TTTGGTGGAGATATT | 51666 |
rs368450255 | snp | C/T | 1.64944e-05 | 0.00287175 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95528022 | AGCACGGAGCACCAC[C/T]TGGTCTGCCGCATGC | 51666 |
rs368495010 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95530378 | GCTGAGGCAGGAGAA[C/T]GGCTTGAACCCGGGA | 51666 |
rs368514560 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | ASB4 | GRCh38.p7 | 7:95536387 | TGTGAGCAGAATGAA[G/T]GAACCATATATGTGC | 51666 |
rs368532581 | snp | A/C | 1.6501e-05 | 0.00287232 | missense | ASB4 | GRCh38.p7 | 7:95527900 | TTTCGGAGCTGGTGG[A/C]CTTCTACGTGGAACA | 51666 |
rs368540825 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95532573 | TATATGAAGGTAGGC[A/G]GTTCTCTTTGATCAT | 51666 |
rs368555891 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95503417 | CTTGGCACATAGAAA[A/G]TGCTCAATAAATAGT | 51666 |
rs368557843 | snp | A/G | | | | | GRCh38.p7 | 7:95464025 | TTAAGTAGTTGAGAC[A/G]AATTATTTTATCTGA | 51666 |
rs368613220 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95499936 | TGGAGTGCAGTGGTG[C/T]GATCTCGGCTCACTG | 51666 |
rs368628140 | snp | C/T | 0.000115398 | 0.00759512 | synonymous-codon, intron-variant | ASB4 | GRCh38.p7 | 7:95537678 | ATTACACAACAGATG[C/T]CATAGAGCAATTCCT | 51666 |
rs368641449 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95509908 | TGTCAGATTCAAGCA[A/G]ATCAAATTTTATTTG | 51666 |
rs368653439 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95495306 | AAAAGATTTTGGATA[G/T]AATAAAAATTATAAG | 51666 |
rs368661684 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASB4 | GRCh38.p7 | 7:95503770 | CCAATGCCATGGCAA[C/G]TGAAAACCGATGTAA | 51666 |
rs368682001 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95522382 | GTAGCTGTTCAAATT[C/T]TACACATGGGCTTAA | 51666 |
rs368850830 | in-del | -/T | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539077 | TCAATTTTGCTTCAC[-/T]TTTTTTTTTTGTTCT | 51666 |
rs368855987 | snp | A/G | | | | | GRCh38.p7 | 7:95467428 | AAAAAAAGAAAACTC[A/G]GTAGTAAGCACTTGA | 51666 |
rs368906583 | snp | C/T | | | | | GRCh38.p7 | 7:95463010 | AGACTTTCTTTTTTT[C/T]TTTTTCTTAAGAGAC | 51666 |
rs368907823 | in-del | -/A | | | intron-variant | ASB4 | GRCh38.p7 | 7:95492525 | CTAGCAGGCTGAAAA[-/A]GTGGCAGTTTTCTCA | 51666 |
rs368957943 | in-del | -/TGTG | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95485003 | GTATATATGTATATA[-/TGTG]TGTGTATATATGTGT | 51666 |
rs369056781 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95504178 | AAATGAAAGCTGCCC[A/G]CTTTACTCTGCATGA | 51666 |
rs369148134 | snp | A/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95462286 | GATTAGTGGGAGGAA[A/T]AAAATGGAATGTGTT | 51666 |
rs369180508 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95517128 | TCCATTTTTAAATTG[G/T]GTTATTTGGCTTTTT | 51666 |
rs369296773 | snp | C/T | | | | | GRCh38.p7 | 7:95481349 | TAACCTATAAAAGAA[C/T]AGCAAAAAAAGGAAA | 51666 |
rs369303946 | in-del | -/A | 0.495999 | 0.0445491 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484026 | TTAACATTAAAAAGT[-/A]AAAAAAAAAAAAAAA | 51666 |
rs369304240 | snp | G/T | | | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95474344 | AGTTGATAATAACTT[G/T]TGTGCTTTGATTTTT | 51666 |
rs369453233 | snp | C/T | | | | | GRCh38.p7 | 7:95465985 | TGAATGCAAGTCTTC[C/T]CAATTAGAATAGTGC | 51666 |
rs369457395 | snp | A/C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95501155 | TTTGTCTCACTTTTC[A/C/G]TAATAATGAAATGAA | 51666 |
rs369486879 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95497645 | TTGTGAAACTATCAT[C/G]CCAATCATCTTAAAA | 51666 |
rs369494091 | snp | A/C | | | | | GRCh38.p7 | 7:95460723 | AAGCCAGCTGCAGAA[A/C]GTTGCACAAGTAATG | 51666 |
rs369829532 | snp | A/G | | | | | GRCh38.p7 | 7:95475261 | ACTCACTACACTATA[A/G]CCAATGACCATCTTT | 51666 |
rs369846638 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95501607 | ATCTTCAGAACTTAT[C/T]CATCATCCGGTGTAA | 51666 |
rs369854893 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95521264 | TAAATAAGAAAAGCC[A/C]AACCCAATGAAAAAT | 51666 |
rs369899206 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95512019 | TATGTCAGTCAGCAA[A/C]CCTGCCACTCCCTCA | 51666 |
rs369922408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95521124 | AAAACTTTCCATTTA[C/T]TGAGTCTTTTGCCTT | 51666 |
rs369976009 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95531570 | TGGTAACCATTAAAC[A/G]AATGATGGCTATGAC | 51666 |
rs369983394 | snp | C/T | 0.00211107 | 0.0324203 | intron-variant | ASB4 | GRCh38.p7 | 7:95486182 | ATATAGGTGTTATTG[C/T]AGAACTGTTAGAAAA | 51666 |
rs370000146 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515231 | TCTTTCTTTCTTTCT[C/T]TTTCTTTCTTTCTTT | 51666 |
rs370042858 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95487456 | GTGCCTAGGGTGAAA[C/T]AACTCAGGTTCAAGT | 51666 |
rs370082531 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95517817 | GGAAAACAGAGACCA[C/T]CCTTTCAAGGAGTTC | 51666 |
rs370098195 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95500158 | CAAAAAATGAGAGGA[C/G]AGCAGAAAGCATAGA | 51666 |
rs370098783 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95497860 | GTTGCATGGACCAAT[A/G]AATTAGACCTTTTTA | 51666 |
rs370146871 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95493603 | GCAATACATGCACAG[C/G]ATACTAAATTTAGAA | 51666 |
rs370213105 | snp | A/G | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95537940 | TAAAGAAGAAGTAAA[A/G]TTAAGGAATTTTCAA | 51666 |
rs370231750 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95506059 | GGCCGTGCCTGGCTA[A/C]TTTTTAAAAAATTAT | 51666 |
rs370333866 | snp | C/G/T | 6.63178e-05 | 0.00575805 | missense, stop-gained | ASB4 | GRCh38.p7 | 7:95527842 | ATGAAGACCAACAAC[C/G/T]AAGATGAGGAGACGC | 51666 |
rs370378408 | snp | C/G | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538347 | GAGAAAGAAACATCA[C/G]TCCAGTTAATAGTCA | 51666 |
rs370439830 | snp | C/G | | | | | GRCh38.p7 | 7:95479003 | GGCTGCCACAGGGAA[C/G]ACTTTCAAAAAATCT | 51666 |
rs370459286 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95512714 | TTTGGGTAATGCTGG[C/T]TTAGAAGAATGAAAT | 51666 |
rs370598365 | snp | A/G | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95485161 | TTTATCCCTTAATGT[A/G]TCACTTAAGAGTAAG | 51666 |
rs370622004 | snp | A/G | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95483766 | TCTGCAGTGCCCAGA[A/G]TAAGTGTCTGACAAA | 51666 |
rs370663407 | snp | A/T | 0.000153988 | 0.00877328 | missense | ASB4 | GRCh38.p7 | 7:95495917 | TTCACGTGGCTTGTG[A/T]AATGGCCAATGTGGA | 51666 |
rs370793680 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95523442 | AACTAAAAAAGAAAT[A/G]CCATTAGTTAATAAT | 51666 |
rs370801824 | snp | A/T | | | | | GRCh38.p7 | 7:95467828 | GGGTCACCATTCACA[A/T]CTCAAGAGGCTTGAC | 51666 |
rs370867451 | snp | A/G | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472620 | TACTCTCACTAATAG[A/G]GGTTTTAATGATGCT | 51666 |
rs370883820 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95522737 | TCTGCTGAAATTCTT[A/G]TCTTATCTGTCCTGT | 51666 |
rs370908721 | in-del | -/TTTT | | | intron-variant, nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471873 | ACTATTATTATCTGC[-/TTTT]TTTTTTTAACAGATG | 51666 |
rs370924699 | in-del | -/TGTGTGTG | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513294 | ATCGAGCCAATAGAA[-/TGTGTGTG]TGTGTGTGTGTGTGT | 51666 |
rs370935035 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95519675 | CTTCTCAAATCCTTA[C/T]GAATAAACCATGATA | 51666 |
rs370956898 | snp | A/C | | | | | GRCh38.p7 | 7:95479935 | GGGTCTTAGAATCTG[A/C]TGCTCCCATGGCCTA | 51666 |
rs370984717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95536107 | GAAAGAAATTGGTTT[A/G]ATTTTATTAATCTAT | 51666 |
rs371005051 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95495739 | AAACTTTCCTTTTCC[C/T]TTTTTTTTTTTTTTT | 51666 |
rs371010160 | snp | A/T | | | | | GRCh38.p7 | 7:95467072 | CTGTGAACTTATATA[A/T]ACGTAAACAGCTTAC | 51666 |
rs371253714 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95503851 | AAGGCTAATTGAGGC[A/G]AAAAATTGCACCCAA | 51666 |
rs371414898 | snp | C/T | 3.29962e-05 | 0.00406165 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95527943 | GGACAGCGTGAATGC[C/T]CACATGGAGACCCCC | 51666 |
rs371416391 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95478171 | AATTTGTCAAAAGTA[A/G]AAAGAGGATGCAAAT | 51666 |
rs371417017 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | ASB4 | GRCh38.p7 | 7:95536598 | CTATCAAGTACTTCC[A/G]GACTGCTCTAGAAGT | 51666 |
rs371840691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95500458 | GTATTCCTAGCTACT[C/T]GAAAGGCTGAGGCAG | 51666 |
rs371982870 | snp | A/C/G | 4.94779e-05 | 0.00497362 | missense | ASB4 | GRCh38.p7 | 7:95528034 | CACCTGGTCTGCCGC[A/C/G]TGCTGCTTGACTACA | 51666 |
rs371984012 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95501244 | TGTTACTGCAGGAAA[A/G]CCATAAAAATTCAAA | 51666 |
rs372143715 | snp | C/T | | | | | GRCh38.p7 | 7:95463016 | TCTTTTTTTCTTTTT[C/T]TTAAGAGACAAGTTC | 51666 |
rs372162562 | in-del | -/TCTT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515162 | TTCTTTCTTTCTTTC[-/TCTT]TCTCTTTCTTTCTTT | 51666 |
rs372178163 | snp | A/G | 0.00438332 | 0.0466095 | | | GRCh38.p7 | 7:95460463 | CTGAGGTGGCCTCAG[A/G]TGGAGATGAGGAACT | 51666 |
rs372193846 | snp | C/G | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538472 | AGCAGAGGATCCAGA[C/G]ATACACACAGCTAAC | 51666 |
rs372221616 | snp | A/G | 0.00159617 | 0.0282053 | | | GRCh38.p7 | 7:95466344 | GAATGTTTATAGTGC[A/G]TGATCACTGTGTAGG | 51666 |
rs372305782 | snp | C/T | | | downstream-variant-500B, intron-variant | ASB4 | GRCh38.p7 | 7:95540426 | TGGCCAAAACACAAA[C/T]ACAATGCAGCCTCTT | 51666 |
rs372379082 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95525513 | GGAACTCCTATTCAG[A/G]AAAGGAAACCATGTA | 51666 |
rs372425293 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95505766 | TTGTGGTCAACTATG[A/G]TAGTTTCTTTTTTTG | 51666 |
rs372429965 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95524986 | TTTGCCAAATAAATT[C/T]TGTAACCACTCACCC | 51666 |
rs372446229 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485882 | TGGGATAAAATTAGC[C/T]GACAGTTTGTGGACT | 51666 |
rs372500270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95495127 | CTTATTTTCTAAATC[A/G]TTTAAAAAATCTTTA | 51666 |
rs372596566 | snp | A/G | | | | | GRCh38.p7 | 7:95461664 | TGTGTTTTGAAATGT[A/G]AGTACATGAGATTTG | 51666 |
rs372612418 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95522529 | TCTACATGTTAGGCA[A/G]GGCATTGTATTTATT | 51666 |
rs372614332 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95516375 | TAAAAAATAAAATAA[A/T]TACAGGGTGACTGAG | 51666 |
rs372727644 | snp | A/G | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539749 | GGGAAGCTTGAGAGT[A/G]GGGTGAGGGATAAAA | 51666 |
rs372735197 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95490724 | CAAAAGAAGGCCCAA[A/G]CACTTTGCTCCTTGC | 51666 |
rs372838435 | in-del | -/TG/TGTG | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513293 | ATCGAGCCAATAGAA[-/TG/TGTG]TGTGTGTGTGTGTGT | 51666 |
rs372903179 | snp | A/G | 1.69619e-05 | 0.00291216 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95537776 | CCTTATGAGACAGCA[A/G]TTCCCAATCCTAGGT | 51666 |
rs372920590 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95497047 | GGTGTGGGGTAGGGT[A/G]GGAAGGACAAGAGGG | 51666 |
rs372932698 | snp | A/G/T | 0.000131894 | 0.00811981 | missense | ASB4 | GRCh38.p7 | 7:95495961 | CTCTGTGATCGTGGG[A/G/T]CAAAGCTCAATTGCT | 51666 |
rs372946531 | in-del | -/A | | | | | GRCh38.p7 | 7:95460844 | AGAGGCCTAGGAGGG[-/A]AAAATGGTTTCCTGG | 51666 |
rs373079716 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95532050 | AGGAGAGCTGGCCCC[C/G]CTCCAAAGGAAAAGT | 51666 |
rs373079972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95531380 | TTTCTGCATATTGTC[A/G]TTCAAAGACTACTTT | 51666 |
rs373085799 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95501991 | TTCAACTTCAGAAGG[G/T]CAAACACCATAAAAT | 51666 |
rs373101368 | snp | A/G | 3.29821e-05 | 0.00406078 | missense | ASB4 | GRCh38.p7 | 7:95495887 | TCAACTGTAGACCCA[A/G]TGGGAAAACCCCTCT | 51666 |
rs373117388 | snp | A/T | 0.0232847 | 0.105357 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469076 | TTTGGAGCTGGGCAG[A/T]TTTAAATTATATAAG | 51666 |
rs373139899 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95507707 | CTAGCACTAGGGAAA[A/G]GAGTGCAGTTGAACC | 51666 |
rs373153333 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95517597 | AAGCACACCCAAGGA[A/G]ACTGAAAAAAAAAAA | 51666 |
rs373161514 | snp | A/C | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95477571 | ATAGAAAACTACAGA[A/C]AGGCAGCGTTGTGTA | 51666 |
rs373244916 | snp | A/G | 1.65682e-05 | 0.00287817 | missense | ASB4 | GRCh38.p7 | 7:95536516 | TCAGATGGAACACAA[A/G]GTGGAGAAGAGCTAT | 51666 |
rs373298545 | snp | A/G | 9.95504e-05 | 0.00705445 | missense | ASB4 | GRCh38.p7 | 7:95486008 | GTCACTAAATCTGGA[A/G]CTGCCAAGTTAGTTA | 51666 |
rs373343989 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95492916 | GCATGACATACAGCT[G/T]AGGAACTCTGCTCGG | 51666 |
rs373500105 | snp | C/T | 1.66499e-05 | 0.00288525 | intron-variant, synonymous-codon | ASB4 | GRCh38.p7 | 7:95528324 | GCTCTGCCCAGTGGT[C/T]AGCAGGTTGAGGAAG | 51666 |
rs373592830 | snp | A/T | | | | | GRCh38.p7 | 7:95462701 | AATTATATGCAAAAA[A/T]TACTAATTTTAGCAA | 51666 |
rs373633493 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95510214 | TTTCTTCCGAAATGA[G/T]TCCCATCAAGGCAAT | 51666 |
rs373652126 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASB4 | GRCh38.p7 | 7:95537353 | TATTTTATCTTATCT[C/T]CTGGGTTCTGAATTG | 51666 |
rs373668393 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95520305 | TTCAGCTGATCTCTC[C/T]AACTCTTCCAGCCAA | 51666 |
rs373671266 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95532708 | GCAGGAAGACTTACC[C/T]TGAATCTCTTTTTTA | 51666 |
rs373720740 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95518718 | TACAAATCTTTAACA[A/G]GGATTCCACTGCAGG | 51666 |
rs373800497 | snp | A/G | | | | | GRCh38.p7 | 7:95464928 | TTATTGACAACAATA[A/G]GTTATTTTTCTCAAT | 51666 |
rs374098922 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515171 | TCTTTCTCTTTCTCT[C/T]TCTTTCTTTCTTTCT | 51666 |
rs374198751 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95509329 | AGAACACCCAGCTAT[A/G]TACCACAGGCCAGAG | 51666 |
rs374232847 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473389 | CCCAAGGCACAGAGA[G/T]GGTAAGCAGTTAAGT | 51666 |
rs374245657 | snp | A/G | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95483964 | CTTTTTGTTGTTGCT[A/G]TTTTTCAAAAATTAT | 51666 |
rs374257962 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95489188 | CTAAATAGTGCTTCC[C/G]AAATTTACAATCTAC | 51666 |
rs374337159 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95530105 | GGAGAAAAAGCAGGG[A/C]AAAAAAAAAAAAAAA | 51666 |
rs374374969 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95521341 | CCTGTAAACATATGA[A/G]AATACACTTTACTGG | 51666 |
rs374408307 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95519703 | ATAATATTTTCTCCA[C/T]GGTCTTTCTGACCTG | 51666 |
rs374424842 | snp | A/C | | | nc-transcript-variant, intron-variant | LOC107986823 | GRCh38.p7 | 7:95471045 | ATGATTTAGTTGATG[A/C]CATATTGATTTCGTT | 51666 |
rs374521090 | snp | C/G/T | 4.99541e-05 | 0.0049975 | synonymous-codon, intron-variant | ASB4 | GRCh38.p7 | 7:95537597 | TTTTTACCACTCTCT[C/G/T]TTTACTGTGTGCTGT | 51666 |
rs374577381 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515906 | ATTCCTTCTCATACA[A/G]TTGGCTTCTAATAAC | 51666 |
rs374582285 | snp | C/T | | | | | GRCh38.p7 | 7:95475508 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 51666 |
rs374593546 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95534615 | TCCACTCTCTGCCCT[C/T]GATGCACTTGTCTTC | 51666 |
rs374615498 | snp | A/C | | | | | GRCh38.p7 | 7:95479622 | TTAAATATTGAATAT[A/C]CACTGATAAAATATG | 51666 |
rs374627639 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASB4 | GRCh38.p7 | 7:95517614 | CTGAAAAAAAAAAAG[A/G]ATTTCAAGAAATGAG | 51666 |
rs374703583 | snp | C/T | | | | | GRCh38.p7 | 7:95465024 | ATGTCTTTAGGAATA[C/T]TGCTACCTTCTGAAT | 51666 |
rs374759323 | snp | C/T | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95470289 | CATTTAAATACAGAT[C/T]GCCTTTTCATTCTGA | 51666 |
rs374770337 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95510605 | TGGTCTCACCTATAC[A/G]ACAATTTTAGGTCAA | 51666 |
rs374771827 | in-del | -/T | 0.0111196 | 0.0737302 | intron-variant | ASB4 | GRCh38.p7 | 7:95511965 | TGGGTGACTTTGCTG[-/T]TTTTGCCTTATTCTG | 51666 |
rs374777901 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95530390 | GAATGGCTTGAACCC[A/G]GGAGGCAGAGGTTGC | 51666 |
rs374787597 | snp | C/T | | | | | GRCh38.p7 | 7:95463002 | TCTCAGGGAGACTTT[C/T]TTTTTTTCTTTTTCT | 51666 |
rs374824064 | snp | C/T | | | | | GRCh38.p7 | 7:95475582 | AGAGATGGGGTTTCA[C/T]CATGTTGGCCAGGCT | 51666 |
rs374846311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95504427 | CCTTCATTTTAATCC[A/G]AAATAGATATGCCTG | 51666 |
rs374853362 | snp | C/G | 0.00318978 | 0.0398085 | | | GRCh38.p7 | 7:95468103 | TGCTGACACATCTAT[C/G]AGCTTTGAGTGGCCT | 51666 |
rs374921893 | snp | C/T | | | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95472031 | GGATCAGAGGAGGAG[C/T]GTGAGTGTCCTCATA | 51666 |
rs374939644 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95531456 | CAGAGAAACATACTC[A/T]ATCACTTTATCCATG | 51666 |
rs374971595 | snp | C/T | 0.000347939 | 0.0131852 | utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485920 | ATGCGCCTGTTTGCT[C/T]GGTGCTGTTCTCTCG | 51666 |
rs374986166 | snp | A/G | | | | | GRCh38.p7 | 7:95483235 | TCACCATGAGGTCTC[A/G]TAAGCTGCACTCTTA | 51666 |
rs375103279 | snp | A/C | | | | | GRCh38.p7 | 7:95465896 | GCAACTATGAGTAAC[A/C]ACTGTACTCCAGCCT | 51666 |
rs375110950 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95522800 | TTCTTTTGCCCACAG[A/G]TGAAATCTGAAAATT | 51666 |
rs375112778 | snp | C/T | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538705 | TGGTTTCTTGGTTAG[C/T]ATTAATACTTTCCCA | 51666 |
rs375120035 | snp | C/G | 0.000153988 | 0.00877328 | missense | ASB4 | GRCh38.p7 | 7:95527959 | CACATGGAGACCCCC[C/G]TGGCCATCGCCGCCT | 51666 |
rs375238419 | snp | C/T | | | | | GRCh38.p7 | 7:95463031 | CTTAAGAGACAAGTT[C/T]TTGTCTTTTTTTTTT | 51666 |
rs375286869 | snp | A/G/T | 3.29855e-05 | 0.00406102 | missense | ASB4 | GRCh38.p7 | 7:95528035 | ACCTGGTCTGCCGCA[A/G/T]GCTGCTTGACTACAA | 51666 |
rs375334971 | snp | C/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95476629 | AGCTGCTGCTTTAAC[C/T]TCCATCTGTGGCTTC | 51666 |
rs375358155 | in-del | -/TCT | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95504489 | CGTTCCATCTTTTCA[-/TCT]TCTGCGTTATACATT | 51666 |
rs375476932 | in-del | -/GAAACACACTT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95487942 | ACTCATGTGTAGAAA[-/GAAACACACTT]GAAACACACTTCTCC | 51666 |
rs375588892 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515616 | AGACGGGGTTTCCCC[A/G]TGTTGACCAGGATGG | 51666 |
rs375768854 | snp | A/G | 0.000134692 | 0.00820535 | utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485921 | TGCGCCTGTTTGCTC[A/G]GTGCTGTTCTCTCGA | 51666 |
rs375785435 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95487298 | AAGACAAAGAAGGGA[A/T]CTATTTTTTAAAAAG | 51666 |
rs375907091 | snp | C/T | 3.30104e-05 | 0.00406252 | missense | ASB4 | GRCh38.p7 | 7:95527888 | CCCACTTCGGCCTTT[C/T]GGAGCTGGTGGCCTT | 51666 |
rs376002645 | snp | C/T | | | | | GRCh38.p7 | 7:95481187 | AGAGCCTTGTTGACA[C/T]TGAGAACTTCTGGAT | 51666 |
rs376007087 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95507209 | ATCTCTGACATAGTC[A/T]CTTATGAATTTTTTT | 51666 |
rs376194640 | snp | C/T | | | | | GRCh38.p7 | 7:95462466 | CCTCATATTTACTTC[C/T]TTTAAAAAAAAAATT | 51666 |
rs376263930 | snp | A/C | | | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95474339 | GTAGCAGTTGATAAT[A/C]ACTTGTGTGCTTTGA | 51666 |
rs376276476 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95502863 | AAAAATTGCTTGATT[A/C]CTATTTGCCCTCAGA | 51666 |
rs376281193 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ASB4 | GRCh38.p7 | 7:95523244 | TGGTACAAAGGAAAA[G/T]GCAAGGGAAAACTTG | 51666 |
rs376356803 | in-del | -/CG | | | intron-variant | ASB4 | GRCh38.p7 | 7:95502391 | ATAGGTACCAGCCTG[-/CG]GGGGGGGGGCAAATT | 51666 |
rs376367154 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, synonymous-codon | ASB4 | GRCh38.p7 | 7:95528333 | AGTGGTCAGCAGGTT[A/G]AGGAAGATTCAAATG | 51666 |
rs376382733 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95535389 | TAACACCAAGTGAAA[A/G]GGGCTTTAGGAGGAC | 51666 |
rs376415383 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95527617 | TGGTTGTCCAGGAGA[C/T]GGCACTGTTGCTTCA | 51666 |
rs376417128 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95530812 | AATGGTCCTTTTGAC[C/T]GCCTTTCAGAGAATA | 51666 |
rs376423884 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95491279 | TAGTGGAGCTTCTTA[A/T]TCAAACAGAACTCTT | 51666 |
rs376429814 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95508632 | ACACAGCACTCAGCT[G/T]CTTGGGTGCAGGCAC | 51666 |
rs376515296 | snp | C/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95463426 | CCCACCCAAATGTCA[C/T]GTCCAGTTGTAATCC | 51666 |
rs376518954 | snp | A/G | 5.01685e-05 | 0.00500817 | missense | ASB4 | GRCh38.p7 | 7:95536536 | AGAAGAGCTATCCCC[A/G]ATGATGACTTGGAGG | 51666 |
rs376530311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95519030 | TTGCTCTAGAAGAAG[A/G]TAGTTCTCAACCCCA | 51666 |
rs376645768 | snp | C/G | | | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95473966 | TTTAGGCTTCACCTT[C/G]CTTAACTGAAAATAA | 51666 |
rs376729208 | snp | A/T | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472368 | AATCTCAATACTATT[A/T]GAACAAATCTCAATA | 51666 |
rs376790701 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95527342 | CTTGCATCAAACTTT[C/T]AGGTTTATCTGCTAT | 51666 |
rs376814974 | snp | A/G | 0.000329799 | 0.0128371 | missense | ASB4 | GRCh38.p7 | 7:95495916 | CTTCACGTGGCTTGT[A/G]AAATGGCCAATGTGG | 51666 |
rs376854036 | snp | C/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95462635 | TTTACACGTAAAAGG[C/T]TTACATAACATGGAA | 51666 |
rs376857538 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95497775 | TCATATACATTAAAA[C/T]ATAAAATATGTAGGC | 51666 |
rs376873570 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95502069 | AAGGGCTTACTATAC[A/G]CAGAAGTTTTTCAAT | 51666 |
rs376899631 | snp | G/T | 3.36355e-05 | 0.00410081 | missense | ASB4 | GRCh38.p7 | 7:95527820 | CTTTATAGGGGCGAA[G/T]GTGAACATGAAGACC | 51666 |
rs376940552 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95497333 | GGCAAGCTCAGATAG[A/G]AAGTTTAGGAGATGG | 51666 |
rs376983454 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513950 | ATTTCGATGCTGGCA[A/T]AAATTACCAGTCCAA | 51666 |
rs377034414 | snp | A/G | | | | | GRCh38.p7 | 7:95460666 | AATTTGCAGCTTTAC[A/G]ATACAGTAGAAAAGA | 51666 |
rs377035609 | snp | A/G | 0.000605919 | 0.0173952 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95537801 | CTAGGTATTTAAGTG[A/G]ACTTGCTGGGTAGAC | 51666 |
rs377108131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95515508 | GCAACCTCTGCATCC[C/T]GTGTTCAAGTGATTC | 51666 |
rs377108178 | snp | C/T | 0.00199481 | 0.0315187 | | | GRCh38.p7 | 7:95475179 | AGGACTCTGAAGTAC[C/T]GAAAAATTTGAGAAG | 51666 |
rs377148648 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95529992 | GCTGGAGGTAGAGCA[A/G]TGAACCAAAGGCCTT | 51666 |
rs377150505 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95511537 | TAATTAATAATAACC[C/G]TGTAATCACAGCTAC | 51666 |
rs377180698 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538714 | GGTTAGTATTAATAC[C/T]TTCCCAGACTCCTTG | 51666 |
rs377360378 | snp | C/G | | | | | GRCh38.p7 | 7:95466767 | CTCACAATCATGGCA[C/G]AAGACAAAGGAAGAA | 51666 |
rs377396501 | snp | C/T | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469808 | TTGGCATACTTTATA[C/T]GCTCAGAATTGAGTA | 51666 |
rs377433205 | snp | C/T | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95483664 | TATGGGAAATGGAGG[C/T]GATCTAGGGATTCCC | 51666 |
rs377446498 | snp | A/G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95518540 | TGTCTTTACAACAGC[A/G/T]TAATTAAGTTTATTC | 51666 |
rs377521071 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95493029 | CACACACATACACAC[A/G]AGGCGTGGAGTTGAT | 51666 |
rs377737508 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95521824 | ATACACATATAAATA[A/C/G]TAAAAAGAACAAAAA | 51666 |
rs377747955 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515229 | TTTCTTTCTTTCTTT[C/T]TTTTTCTTTCTTTCT | 51666 |
rs386715891 | multinucleotide-polymorphism | CTG/TGC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95502389 | AAATAGGTACCAGCC[CTG/TGC]GGGGGGGGGGCAAAT | 51666 |
rs386715892 | in-del | CTA/T | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539085 | TTTTTTTTGTTCTTG[CTA/T]TAATCACTTTTAGAT | 51666 |
rs397714601 | in-del | -/A | 0 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95521699 | ATTAAAAAAAAAAAA[-/A]CAGTTCTCTATTCAA | 51666 |
rs397736683 | in-del | -/G | 0 | 0 | | | GRCh38.p7 | 7:95468151 | ATTGGGTTGGGGGGG[-/G]CCCCATTCAACCTAA | 51666 |
rs397795565 | in-del | -/C | 0.5 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95505698 | GTGTCCCCCCCCCCC[-/C]AAATACTTATTCATT | 51666 |
rs397819099 | in-del | -/T | | | | | GRCh38.p7 | 7:95477931 | TGCAATTTTTTTTTT[-/T]CCTGCAATATCCCAT | 51666 |
rs397824565 | in-del | -/T | | | | | GRCh38.p7 | 7:95462400 | AAGTTCTTTTTTTTT[-/T]CTAAGACATCTTGTT | 51666 |
rs397829188 | in-del | -/T | 0 | 0 | | | GRCh38.p7 | 7:95477750 | CTTTTTTTTTTTTTT[-/T]GCTATAATTCTGTGA | 51666 |
rs397888943 | in-del | -/A | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484044 | AAAAAAAAAAAAAAA[-/A]TTGTCAGGCATAGTG | 51666 |
rs397889675 | in-del | -/AT | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484964 | CACACACATATATAT[-/AT]GTGTGTATATATGTA | 51666 |
rs397890366 | in-del | -/A | | | intron-variant | ASB4 | GRCh38.p7 | 7:95524506 | CAATAATTAAAAAAA[-/A]CTGTACATATATATT | 51666 |
rs398005491 | in-del | -/T | 0 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95502116 | ACCTCTTTCTCTCTC[-/T]TTTTTTTTTAGTTGT | 51666 |
rs398085987 | in-del | -/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95486845 | TAGACCAATTTTTTT[-/T]TACCAAGGAATTTTC | 51666 |
rs398085988 | in-del | -/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95520647 | CCCACTCCCCACCCC[-/C]CATCCCCATCCACAC | 51666 |
rs398095243 | in-del | -/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95502401 | GCCTGCGGGGGGGGG[-/G]CAAATTGATAACACA | 51666 |
rs398111599 | in-del | -/T | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473655 | TTTTTTTTTTTTTTT[-/T]AATCAACGGAATAAT | 51666 |
rs398111600 | in-del | -/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95521802 | AATAGTATATTTTTT[-/T]AAATGGATACACATA | 51666 |
rs527280854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95502919 | GAAAAATGCTTACAT[A/G]TCTAATAGAAAATTT | 51666 |
rs527417595 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95503634 | GTCACAGATACTCTG[G/T]GGGAGAACTCAAATA | 51666 |
rs527430788 | snp | C/G | 1.6537e-05 | 0.00287545 | missense | ASB4 | GRCh38.p7 | 7:95495769 | TCAGGTTACTGGTTG[C/G]CTAGCTATAAATTGA | 51666 |
rs527454501 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95482060 | GGCATTGCTTCCTAT[C/G]TTAGAAGGACTTTGA | 51666 |
rs527460930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95517753 | AGTGTGGGGACAGAG[A/G]CAAGGTTTGATGGAC | 51666 |
rs527465543 | snp | A/G | 0.000399281 | 0.0141238 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95473983 | TTAACTGAAAATAAA[A/G]CCATAAGTTACCTCC | 51666 |
rs527548004 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95518306 | CCAGGCTTAGACAAT[G/T]AAAAGTCCATGAGGA | 51666 |
rs527578755 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95466928 | CAATTACCTCCCACC[A/G]GGTCCCTCCCATGAC | 51666 |
rs527598302 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95466483 | TAGTTTGGGAAAATG[C/G]ATATTTGTAAACATA | 51666 |
rs527661867 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95491993 | ATACACTTCAGTATA[C/T]CCTAAGCTATAGCCT | 51666 |
rs527750979 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95512465 | AGTCCACTGTATTAA[A/G]CAATGATGCTGGAGC | 51666 |
rs527779842 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95460836 | ACAGGCCCAGAGGCC[C/T]AGGAGGGAAAAATGG | 51666 |
rs527792370 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95468975 | CATTTCTTTATCAGT[A/T]CAAAAAATAATTTAT | 51666 |
rs527909979 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95496626 | CTAAGGTGAGAGGAT[A/C]ACTTGAGCCCAGGAG | 51666 |
rs527916760 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539553 | TATTAGAACACATCC[A/T]AAAACAGAATGAAAT | 51666 |
rs528023633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95490567 | CCTTTGGCTGTAATA[A/G]CAGAGGCTTCTCATG | 51666 |
rs528023669 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95482920 | AAGTTCGAGGACACT[A/G]AGGTTAGCGGCTCAG | 51666 |
rs528053262 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484312 | GCTCCAGTCTGGTGA[C/G]AGAGTGAGATCCTGT | 51666 |
rs528094904 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95498750 | AAATTTGTTTCATAT[A/G]TTTATTTCTAGAGGT | 51666 |
rs528120623 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95534976 | CTGGCTTCATCTTAC[A/C]AGCTCTGACCTTTAG | 51666 |
rs528176783 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95478162 | TGCATCATAAATTTG[C/T]CAAAAGTAAAAAGAG | 51666 |
rs528189404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95535327 | AGAAATGTCTTTGGA[A/G]AAAGTTGTTTAAGTG | 51666 |
rs528238693 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95527094 | CATTTTCTCTCTTTC[A/G]ATGAATATTTCTACT | 51666 |
rs528251024 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95494028 | AAGTCCAGGAGCACA[A/T]TTCACAGAGTACAAT | 51666 |
rs528265318 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ASB4 | GRCh38.p7 | 7:95505693 | TATCCGTGTCCCCCC[C/G]CCCCCAAATACTTAT | 51666 |
rs528279379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95504889 | TGAAATGAGTTTGCA[A/G]TCCCTATCTCACACC | 51666 |
rs528515665 | in-del | -/A | 0.157972 | 0.232445 | intron-variant | ASB4 | GRCh38.p7 | 7:95510126 | TTAAAGGCTTTTCTT[-/A]AAAAAAAAAATGAGA | 51666 |
rs528620629 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95493304 | ATAAAGGGAAAGGTG[G/T]GAGAGAGAGAAAGCA | 51666 |
rs528655468 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95491941 | CAAAAATCCCTAGCC[C/T]CACATTACCACCAAA | 51666 |
rs528655996 | snp | A/G/T | 0.000399281 | 0.0141238 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471213 | TACAGGAAAAAAGAC[A/G/T]CACGTCCCCTTCAAA | 51666 |
rs528666194 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95514193 | CTCACCCTCTCTTAA[C/T]GTCATTTCTTTCTCT | 51666 |
rs528667301 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95479008 | CCACAGGGAAGACTT[C/T]CAAAAAATCTCAGCA | 51666 |
rs528699335 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95509848 | TATTTAAAAAATGAG[A/G]AATCGGAGACTCAGA | 51666 |
rs528702857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95529442 | GGGACTTGTCTGAAG[C/T]CCTGCAGTGTGAGGC | 51666 |
rs528776208 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95462955 | AGGTGAGAATCCTAA[C/G]GGAAACCCAGAGAAA | 51666 |
rs528790416 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471622 | AAATAAACAATAATT[A/G]TCTAATTTTGGCCCT | 51666 |
rs528859810 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95505673 | GGATCTGGCTCCTTT[A/T]CCTCTATCCGTGTCC | 51666 |
rs528883686 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95540229 | AGCTCTTCTGTCTCC[C/T]TTCATCTTTGTGTTT | 51666 |
rs528897184 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95497561 | TTTTTTAAAAAGTCA[C/G]TTTATGGAGGTATAA | 51666 |
rs528931496 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95478087 | AGAACGTTACAGAGG[A/G]CAGTCCAATTTCTTT | 51666 |
rs528949238 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95529777 | TCTAAATAGGTTTTA[A/T]ACAGACTATTTCATT | 51666 |
rs529066780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95520406 | AACAAGCTCAACTGG[C/T]GGAAGAATAAAAAAA | 51666 |
rs529073810 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95526340 | CGCACAATGACCTCC[C/T]TCAGCACAGCAGCTC | 51666 |
rs529129757 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95460035 | CTCTCCTGATACCTT[C/G]TGAAGAAGGATGTAT | 51666 |
rs529213995 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95504611 | AATATGAATTTAATG[C/T]TGTCATCAAATTGAT | 51666 |
rs529218860 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95460667 | ATTTGCAGCTTTACA[A/G]TACAGTAGAAAAGAA | 51666 |
rs529279707 | snp | A/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95462382 | TATGCTCTTTTATTT[A/T]AAAAAGTTCTTTTTT | 51666 |
rs529292459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95514956 | TCACCTAAGGGGCTG[C/T]TCTAAACCTTTATGT | 51666 |
rs529411192 | snp | A/T | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95483788 | TCTGACAAATGGTAG[A/T]TACTCGATGGGTATT | 51666 |
rs529448814 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95514645 | AGATAGTCTCAGATG[A/G]TTAGTCACTACCTGT | 51666 |
rs529456268 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95477524 | TTATTTTTTCTTTAC[A/G]CTATCAGTTTAGGGA | 51666 |
rs529532225 | snp | A/C | 1.64974e-05 | 0.00287201 | missense | ASB4 | GRCh38.p7 | 7:95527934 | GGCCATAGTGGACAG[A/C]GTGAATGCCCACATG | 51666 |
rs529535026 | snp | A/C | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95461687 | GAGATTTGGGAGGGA[A/C]CAGGGTGGAATGATA | 51666 |
rs529566209 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95478044 | TTGGTAAACAACTTA[C/T]TGGCTTCTGACAACT | 51666 |
rs529585120 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASB4 | GRCh38.p7 | 7:95513492 | GGGAGGTTAGTCTTC[A/G]TTCTATGAAGACTTT | 51666 |
rs529596876 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95470428 | TTTTATGCTTTTTTT[A/T]AAAAAAACTCTTAAT | 51666 |
rs529706141 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95516135 | CTTCTAAAAAAATCA[A/G]TCTTCCTCAGGGTTA | 51666 |
rs529714777 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95535988 | GGGAATGTATTCTGT[A/G]TCCAGTCTGTCTCTA | 51666 |
rs529734179 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95523205 | CAAGATTGTTATGCA[A/G]CTTCTGAAAGGAGTA | 51666 |
rs529756600 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472393 | TCAATAATATTTGAA[C/G]ATTTTGCACTGGGCC | 51666 |
rs529761586 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95524168 | CTGCACGTGAGCACC[A/G]GAGTACAAGAATGTG | 51666 |
rs529786604 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473019 | GATTGCTCACCAGTG[G/T]CAAGTTTCCATGGAG | 51666 |
rs529800000 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95493244 | CCTCAGTCCATTAGA[C/G]CTTAATGTGAAATAA | 51666 |
rs529807096 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95463761 | TCAGGTATTTCTTTA[C/T]AGCAGTGTGGGAACA | 51666 |
rs529954992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95529584 | AATCCTGTGATCTCA[A/G]TAGGAATTTTCTCTT | 51666 |
rs529975560 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95493801 | GTTTGGCTCCCTGCT[C/T]CTCTCATTCAGTAAT | 51666 |
rs530063060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95495000 | TTTTGGCTGCTAGGA[A/G]ATTCAAAGGCAAATT | 51666 |
rs530091482 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95532212 | AAGTGATTCGTTCTT[A/G]TGTGGATGGGGAATT | 51666 |
rs530160577 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASB4 | GRCh38.p7 | 7:95515891 | ACTGTTGCTTGACAA[A/G]TTCCTTCTCATACAA | 51666 |
rs530176967 | snp | A/G | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95540098 | ACCTTGCTTGTGCTT[A/G]AACACTTATGTTCAT | 51666 |
rs530360952 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95501329 | AAAGACTGTTCCCTG[C/T]TACTTTATCTGACAG | 51666 |
rs530412013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95529481 | AAGAAAAGTTCTACT[A/G]GAGAATTTAAGGGTA | 51666 |
rs530471374 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95528840 | TTACAACAATCATAC[A/G]AGGTATATATTATTA | 51666 |
rs530473028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95536020 | ATTGCTTCAATTATG[C/T]ACAAAGGCAAAGTAA | 51666 |
rs530488915 | snp | A/C | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95478182 | AGTAAAAAGAGGATG[A/C]AAATGCTGCCTGGAG | 51666 |
rs530494935 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95523068 | TGTATGTCTGCATGG[A/G]AGGACTCCATACTGT | 51666 |
rs530499091 | in-del | -/A | 0.160938 | 0.233598 | intron-variant | ASB4 | GRCh38.p7 | 7:95517601 | CACCCAAGGAAACTG[-/A]AAAAAAAAAAAGAAT | 51666 |
rs530574425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95498829 | ATTTTTTTATATGGT[A/G]TAAGTTATGGGTTAG | 51666 |
rs530610043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471722 | AGAGGACAGCAGTGG[C/T]GGCAACAGTGGAGTT | 51666 |
rs530636135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95498323 | ACATATTAGAATAGC[C/T]AACATATTGGCTAAC | 51666 |
rs530755913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95492292 | TAGGTGCTACCTGGA[A/G]GTTAGGAGGAGGAAA | 51666 |
rs530826087 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95492242 | AGAGGCCAAGGATGA[C/T]TGACTCACATAATAC | 51666 |
rs530868356 | snp | C/T | 1.67083e-05 | 0.00289031 | missense, intron-variant | ASB4 | GRCh38.p7 | 7:95537593 | GGGATTTTTACCACT[C/T]TCTCTTTACTGTGTG | 51666 |
rs530881871 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95501255 | GAAAGCCATAAAAAT[A/T]CAAATGTTTCTTAGC | 51666 |
rs530890486 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95487435 | GTTTTTAAAAAGCTT[A/G]TATTTGTGCCTAGGG | 51666 |
rs530997897 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95509935 | TTTGTTTTGGGTCCG[A/T]GATGCTCCCACTGTG | 51666 |
rs531009982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95516064 | GAGTCCAGAACAGAC[A/G]GAATTTTGTCCCTGA | 51666 |
rs531020769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95523631 | TATTAATAAAGACTC[C/T]TAACATAGTTCAAAT | 51666 |
rs531072337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95486674 | AGGCACCTTCATGGT[C/T]TTCTTCATTTTAATG | 51666 |
rs531146070 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ASB4 | GRCh38.p7 | 7:95515268 | TTCTTTCTTTCTTTC[C/T]CTTTCTTTCTTTCTT | 51666 |
rs531154862 | snp | A/G | 0.00159617 | 0.0282053 | | | GRCh38.p7 | 7:95463115 | AGTGGCATGATCATA[A/G]CTCACTGGAACCTTG | 51666 |
rs531155064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472241 | CCCAAAAATGTGTCC[A/G]AAATTGAAAGTGCCA | 51666 |
rs531191636 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95487322 | TAAAAAGTTTATGGG[A/G/T]TCTGTTAGAAAATTT | 51666 |
rs531233597 | snp | C/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95466343 | AGAATGTTTATAGTG[C/T]GTGATCACTGTGTAG | 51666 |
rs531245763 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95463690 | AGCCATGCTTCCTGC[A/G]CAGCCTGTGGAACTG | 51666 |
rs531331664 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95502102 | AAGTAATGAGGCTAA[C/G]AACTAAAAAAAAAAG | 51666 |
rs531344017 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95517713 | TACAGGCCACTAGTG[A/C]TCTTCGTCTGAGCAG | 51666 |
rs531353681 | snp | A/G | | | | | GRCh38.p7 | 7:95480050 | TTATTTGAATTTGCA[A/G]TGCTTTCCAGGGCCA | 51666 |
rs531368679 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95480778 | CAGAAACCATGAGAG[A/G]TAATAAATGATGACT | 51666 |
rs531373404 | snp | A/G | | | | | GRCh38.p7 | 7:95477540 | CTATCAGTTTAGGGA[A/G]AGGAGATGCAAAACT | 51666 |
rs531454136 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95531467 | ACTCTATCACTTTAT[C/T]CATGAATAGTAATAG | 51666 |
rs531455252 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95526553 | CAGCTAGTTGCACTC[A/G]TGACAACTAGCTGGT | 51666 |
rs531489726 | snp | C/G | 0.000399281 | 0.0141238 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95473950 | GGGACATTTCTTAAT[C/G]TTTAGGCTTCACCTT | 51666 |
rs531491530 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95465384 | TGTATATAAGTAAAA[C/T]TAATTTCTATGGAAT | 51666 |
rs531503686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473288 | GCCCTAGATACCCTT[A/G]TAAGGGCTTTACACA | 51666 |
rs531518651 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95532133 | ACTACTCCACAGCCC[A/G]ACTTTCCAAAGAGAA | 51666 |
rs531519410 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95524373 | GAAGCAAGTCAAAAG[A/G]ATTTGTGTTTATGAT | 51666 |
rs531575425 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | LOC107986823 | GRCh38.p7 | 7:95474680 | GCACATGCCACCATG[C/T]CAGGCTAATTTAAAA | 51666 |
rs531611463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95517136 | TAAATTGGGTTATTT[G/T]GCTTTTTCTATTGAG | 51666 |
rs531611567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95524952 | AACCCCTCTTACTTT[A/G]CTGAGAGTCTTTTTC | 51666 |
rs531633094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95525715 | GAAGACATTCTCATT[C/T]GTTCCATTTCACTCC | 51666 |
rs531641353 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95505050 | CTCTTTAGAATCACG[A/T]ATGAAACAACTTTTC | 51666 |
rs531699610 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95482872 | CTTTGATGGGATGGG[A/G]GGTGGTTTAGAAACA | 51666 |
rs531741015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95495655 | CCACCCCACTTTTAT[A/G]AATGTGGCCAAAATA | 51666 |
rs531771046 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95533554 | TCTGTCTTCATCTCT[G/T]GATCTTCATGACCCC | 51666 |
rs531834725 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95468210 | GCAATATACACAATA[A/G]GTAATAAATTCTGGG | 51666 |
rs531864748 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95506158 | CCTGCCTAGGCCTAC[A/G]AAGTGCTGGAATTAT | 51666 |
rs531948049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95502672 | ACTAGAAATTAGAGA[C/T]TTTCTCCTAATTCTG | 51666 |
rs531955163 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473129 | GCAGAAACTAGGAGA[C/G]AAAAAAAGTCAAATT | 51666 |
rs531995729 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539311 | TAACTGGTTAATCTC[A/G]GTTGAGACTGTGCTT | 51666 |
rs532018118 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95524269 | AAATTGTGGATTACT[C/T]GTGCTAAAAGACAGA | 51666 |
rs532166029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95486651 | ATAAATGGATAAAGC[A/G]GTGCCACAGGCACCT | 51666 |
rs532169727 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471537 | TAGCAATTATATTTG[C/T]ATGAGAGTTGAAGGC | 51666 |
rs532261575 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472474 | ACTAGTAACTCCAAT[C/T]TGCCGGGGGAAACAA | 51666 |
rs532261636 | snp | C/T | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:95480696 | AACCCCCGACCTTTG[C/T]GTCTTTAGTTTGAGG | 51666 |
rs532318258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95537485 | AGCTGCCATTACGTA[C/T]AGAGGTTAGTTGCAG | 51666 |
rs532331398 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95530315 | AATAAAATACAAAAA[A/C]TTAGCTGGGTGTTGT | 51666 |
rs532353742 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95532906 | CTTCTGTTTTCTGGG[A/C]TGGCAAGGTCAAAAG | 51666 |
rs532355599 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513740 | AACTGTAAATAATCA[A/G]TTTGTGTTGTTTTCA | 51666 |
rs532393398 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95492394 | CTTTCCTTGTGATTT[A/G]TGAAGCAGGCTTGGA | 51666 |
rs532422654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95488443 | GTTAGGAATGGAAAT[A/G]ACAAATAGAATCCTA | 51666 |
rs532476813 | in-del | -/TGCATTTCTGTATACCAG | 0.00358779 | 0.0422022 | intron-variant | ASB4 | GRCh38.p7 | 7:95505296 | TATACAAAAATCAAT[-/TGCATTTCTGTATACCAG]AAATAAGCAGCTAGA | 51666 |
rs532496072 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95489214 | TCTACTGGGCACACC[A/G]GTAATCAAAAGTTTA | 51666 |
rs532518904 | snp | A/G | | | missense | ASB4 | GRCh38.p7 | 7:95536465 | GCCATTCTTGTCCTA[A/G]AGCAATTGAAGTTGT | 51666 |
rs532529910 | snp | A/G | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538806 | GGAAAGAAAGTGTGT[A/G]AGGGGACCTAGTTGA | 51666 |
rs532547471 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95489240 | GTTTAGCTCATAAGC[A/C]AATATGAAATGTGTA | 51666 |
rs532562902 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ASB4 | GRCh38.p7 | 7:95502062 | TATGACAAAGGGCTT[A/C]CTATACGCAGAAGTT | 51666 |
rs532622036 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515600 | TTTGTGTTTTTCATA[G/T]AGACGGGGTTTCCCC | 51666 |
rs532636774 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | LOC107986823 | GRCh38.p7 | 7:95474594 | TGGTGCAATCACGGC[G/T]CACTGCAGCCTTAAC | 51666 |
rs532683878 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95517591 | AGAAGAAAGCACACC[C/T]AAGGAAACTGAAAAA | 51666 |
rs532688184 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95482135 | ATCTGTAAGTTTTAT[C/T]CTTTGCTGCTCAGGT | 51666 |
rs532734105 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ASB4 | GRCh38.p7 | 7:95536651 | TTGGTTTTGAGAATG[A/C]CTTTAAAGCGTACTC | 51666 |
rs532769763 | snp | A/G | | | | | GRCh38.p7 | 7:95481309 | TACTTACAAACAAAG[A/G]CATCTTTATGCTAAG | 51666 |
rs532785078 | snp | A/T | | | | | GRCh38.p7 | 7:95459933 | AATCATGGGGGCGAT[A/T]ACCCTTATGTTGTTC | 51666 |
rs532908741 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539664 | ATATGTTCTCACTTA[C/T]AAGTGGGAGCTAAGC | 51666 |
rs532910102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95496656 | GTTCGAGACCAGTCT[C/T]GGCAACATAGGGAGA | 51666 |
rs532912062 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95504514 | TATACATTGTAATAG[A/C]ATAAATCTGACCATG | 51666 |
rs532967235 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95526109 | AGAGAGTAAACTACA[G/T]AAAAATTTTCCTTCA | 51666 |
rs532974954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95511140 | ATTGGATGCTAAGAA[C/T]CAAGCACATGCCAGC | 51666 |
rs532989465 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95518536 | TGAGTGTCTTTACAA[C/T]AGCATAATTAAGTTT | 51666 |
rs532997329 | in-del | -/A | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:95467413 | GGGTGGGGTGTGGGG[-/A]AAAAAAGAAAACTCA | 51666 |
rs533024979 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASB4 | GRCh38.p7 | 7:95490719 | TCTTCCAAAAGAAGG[C/T]CCAAACACTTTGCTC | 51666 |
rs533060969 | in-del | -/CTT | 0.00119737 | 0.0244387 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95483519 | CAAAATTAAATTGTC[-/CTT]CTTTTTGCCACTGAG | 51666 |
rs533064144 | in-del | -/TTAGCGCTGAA | | | | | GRCh38.p7 | 7:95478894 | TGAATACGCCGAACT[-/TTAGCGCTGAA]GCATCTTAGCAGTTC | 51666 |
rs533102223 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95497444 | GTCCCAAGTATCATT[G/T]CCTGGTTTCAGGTTT | 51666 |
rs533145308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95519521 | ATACCAGCCCAGCAG[C/T]GTTTTGTACTGAGGC | 51666 |
rs533275040 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95468123 | TTGAGTGGCCTCATT[A/G]TTTTTTTATTAAATT | 51666 |
rs533287608 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95511818 | GAGACAAATTGCTTA[A/T]TAGTGAAATCAGGTT | 51666 |
rs533294522 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95514009 | CAATTCTAACAATCT[G/T]CATTTCACTCCAGGT | 51666 |
rs533431062 | snp | A/G | 0.0023933 | 0.0345097 | | | GRCh38.p7 | 7:95477122 | TTTTTTTTTTTCCCC[A/G]GGATACTGCAGCTGT | 51666 |
rs533501525 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484135 | GAGTCGGAGATCAGC[C/T]GGGGGAACATGGCAA | 51666 |
rs533559152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95494699 | CTATGGCTATTGGCA[C/T]TGACATAGAAAGAAG | 51666 |
rs533610731 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95520390 | TATTGGAAAGTATAC[A/G]AACAAGCTCAACTGG | 51666 |
rs533637898 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95527678 | GAGCCTGGGGGCAAA[C/G]GGGTTGAGGGTTGGG | 51666 |
rs533791334 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95496104 | CTGCTTGTACACTCA[C/T]GGTTTCAAGACTTTG | 51666 |
rs533803896 | snp | A/C | 0.00279162 | 0.0372561 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95537931 | ATGGGGAAATAAAGA[A/C]GAAGTAAAGTTAAGG | 51666 |
rs533816782 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASB4 | GRCh38.p7 | 7:95501581 | ACTATAGTCATCCTG[C/T]TATACATTAGATCTT | 51666 |
rs533831268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95532509 | GGAGGAAAAGGTAAC[A/G]CGAGGGTCTGGGAGA | 51666 |
rs533912620 | snp | C/T | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:95468309 | TGAGGCAAAAAAGTC[C/T]CCAGGATAAAGAGGC | 51666 |
rs533912779 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95535091 | ACACACATGCGCACA[A/C]TCTTACTTAGTTGGA | 51666 |
rs533916137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95503158 | TAAGCAATTTCAAAA[A/G]GGCAAATCTGTTATT | 51666 |
rs533925085 | snp | A/G | | | | | GRCh38.p7 | 7:95461262 | CATGAAAACAGCCAG[A/G]ATGGAAGTTGTACCC | 51666 |
rs533957343 | snp | A/C | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95465602 | ACTCCTGGCTTCAAG[A/C]AATCCTCCCTCCTTA | 51666 |
rs533959963 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95509205 | GGAGATTAGGTGGTA[A/T]AGCTGAAAAAGCAAA | 51666 |
rs533998147 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95504130 | TGGCTGCTAAGCAGC[A/G]TATTATTTCTACCTA | 51666 |
rs534021104 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95517147 | ATTTGGCTTTTTCTA[C/T]TGAGTTGTAATAGTT | 51666 |
rs534099968 | in-del | -/AGTGAGAAA | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95527729 | AGTTAAAAGAGAAGC[-/AGTGAGAAA]AGTCTTGTTTAATGA | 51666 |
rs534145359 | snp | A/G | | | | | GRCh38.p7 | 7:95476550 | ACACTAGAAAAGACC[A/G]GGGCTGGGAAACGGG | 51666 |
rs534147426 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95481740 | CCTGCTGTCTCAGCC[A/G]TGGGTCCCCAGAGAG | 51666 |
rs534173598 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95525369 | TCAAAGTTCCCAGGA[A/G]TTGATGTTTCTGGTC | 51666 |
rs534295894 | snp | A/G | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:95460097 | CTCCCCCAGCCATGT[A/G]GAATTGTAGGTCAAT | 51666 |
rs534302628 | in-del | -/A/AA | 0.00358779 | 0.0422022 | intron-variant | ASB4 | GRCh38.p7 | 7:95511662 | GCAAAACTCCGTCTC[-/A/AA]AAAAAAAAAAAATAA | 51666 |
rs534389070 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ASB4 | GRCh38.p7 | 7:95521687 | TCAGCAGTTGAAATT[A/T]AAAAAAAAAAAACAG | 51666 |
rs534485626 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95505658 | TCTAATGGAAAATGA[G/T]GATCTGGCTCCTTTT | 51666 |
rs534511687 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95497633 | GAAATATTGTTTTTG[C/T]GAAACTATCATGCCA | 51666 |
rs534513804 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95526583 | TTGTACTTTTGGCCA[A/G]TTATTAACCTCTCTG | 51666 |
rs534526689 | in-del | -/A | 0.00119737 | 0.0244387 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469227 | TCAAAGTAAAATTAT[-/A]AAACAACTGACATGC | 51666 |
rs534539347 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539853 | ATGTATCCATGTAAC[A/C]AAAAACCACCTGTAC | 51666 |
rs534564358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95534303 | AGCTGAGATTGCACC[A/G]TTGCACTCCAGCCTG | 51666 |
rs534574577 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95522275 | TTAGAACTTTACCAA[C/T]AATTTTTTTTATTTT | 51666 |
rs534633160 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ASB4 | GRCh38.p7 | 7:95540256 | GTTTACTTACCAATA[A/C]GACTCTTTTTCCTAA | 51666 |
rs534701572 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95461051 | TGCTGCAGGGGCAAA[G/T]TCCTCATGGAGAACA | 51666 |
rs534703961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95492574 | TGGACTGGATAATCT[C/T]CCCTCCAGCGCTAAC | 51666 |
rs534759249 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95477638 | GGAGACTTCGCTTTG[C/T]GACTAATTAATTATG | 51666 |
rs534762761 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95530930 | AGAATCATGGACTTT[C/G]GGGTCAAACTTGGAT | 51666 |
rs534803132 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95516198 | TTAATTTCCTTCAAC[A/G]AAAACACCTTTCTGA | 51666 |
rs534841606 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95485363 | ACCTAAAAGAGTCCC[C/T]GCCCCGGACCGTCTC | 51666 |
rs534878883 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95461875 | AAAACCATCAACTAA[C/G]TGGGGCTTAAAAGGG | 51666 |
rs534944573 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95514120 | TCTCAGTTACACTGC[A/G]CCAATTCTTTAATGT | 51666 |
rs534946468 | snp | G/T | | | downstream-variant-500B, intron-variant | ASB4 | GRCh38.p7 | 7:95540304 | AGCAATGACACTGAA[G/T]AACTCTACACATTTC | 51666 |
rs535025066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95499155 | GAAAATGTCAAGGAT[A/G]CACTTTATATAAAAG | 51666 |
rs535034589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95491622 | CAGTTAATTGTGTTT[C/T]TAGCATGCTGTGGTC | 51666 |
rs535077330 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95536196 | GTTTTAGCATTCCAG[A/G]GAGCTTAATAGGTCT | 51666 |
rs535159284 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95468656 | ATGATTATTTTTAAC[C/T]GTCATTTAATTTTGT | 51666 |
rs535161687 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95518919 | GAGTCACTGGGAGTT[A/T]GTAAGATTATAGATA | 51666 |
rs535179102 | snp | A/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95476397 | ATTCTTTTTTATATT[A/T]AAAAAAAAATTTATA | 51666 |
rs535217862 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | ASB4 | GRCh38.p7 | 7:95534304 | GCTGAGATTGCACCA[C/T]TGCACTCCAGCCTGG | 51666 |
rs535219694 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95521562 | ATTTCTTCCTCTCAA[A/G]TAACTACTGCACAGT | 51666 |
rs535223415 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95506232 | TTCTGAAATATTTAA[A/G]CTCAGTGGGTATTTT | 51666 |
rs535339614 | snp | A/G | | | | | GRCh38.p7 | 7:95482483 | AAGGACAATCTGTCC[A/G]TTGATCAGCTTTAAG | 51666 |
rs535358571 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95498546 | AGAAATGGGTTGCCT[A/G]TATTCTTATTGATTT | 51666 |
rs535366669 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539029 | ATGTAGGTGATTAAG[C/T]TCTGGGCCTTGTGGT | 51666 |
rs535405783 | snp | C/T | 0.000798403 | 0.0199641 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95474526 | TTTAAAACTTAGTTT[C/T]TGTTTTTCTTTTTGA | 51666 |
rs535439126 | snp | A/G | | | | | GRCh38.p7 | 7:95478114 | CTTTACCCCTTAAAA[A/G]GGAAGGATAATTTTT | 51666 |
rs535458379 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95490255 | CCACTCTCTGAATGA[A/T]TAATTTCTTTATCAC | 51666 |
rs535459828 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ASB4 | GRCh38.p7 | 7:95533800 | GGCTGAGCAAGTTAA[A/C]GTATATGAAGATTTA | 51666 |
rs535495345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95520025 | TTGTTTGGAGATGAA[A/G]TGGGTAGGTTCAGTT | 51666 |
rs535551361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95526552 | CCAGCTAGTTGCACT[C/T]GTGACAACTAGCTGG | 51666 |
rs535578161 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95475674 | CAGGCATGAGCCACC[A/G]TGCCCGGCCTTGAAT | 51666 |
rs535589108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95491577 | TTGCTGTGGGAAGAA[A/G]GGAGTGTGTAAAAAA | 51666 |
rs535621900 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469295 | TTTTGAGGTCAAAAG[C/G]CCCTCAGATGAGGAA | 51666 |
rs535750860 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95461010 | GCCTTGGCAGCTTAC[A/G]TGTGGAGGATGTCCA | 51666 |
rs535782158 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95489679 | TTGCGTTTACCAGAT[A/G]ATCACTTTAAAATAA | 51666 |
rs535815300 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B, intron-variant | ASB4 | GRCh38.p7 | 7:95540414 | AAAGGGTAACTGTGG[C/T]CAAAACACAAATACA | 51666 |
rs535823355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95515357 | TTTCTTTCTTTTTCT[C/T]TCTTTCTTTTCTTTC | 51666 |
rs535832107 | snp | A/T | 0.00557542 | 0.0525036 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95468908 | GTTCTTTAAAAATTT[A/T]AAAAAATCAGTGCTC | 51666 |
rs535854429 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95497828 | TTAGCATAATACATT[G/T]GAGATCCATCCATAT | 51666 |
rs535871978 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95498278 | GAGTTTGAGTTCAGC[A/G]TGGGCAACATCAGTT | 51666 |
rs535915031 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95507407 | CAAACTTCTACTCCT[C/G]TGCGAAGTCTTAGTT | 51666 |
rs536001493 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95485109 | ATCTGTCTGCATTTC[C/T]GAGCTATTTTTAAAG | 51666 |
rs536038270 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95497545 | ATAATCATTAAATCC[A/G]TTTTTTAAAAAGTCA | 51666 |
rs536043442 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95512775 | TTTGGTGCAGCAAGA[A/G]CTCCATTTAGCCCTG | 51666 |
rs536046765 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95526854 | CCCTAAGGGTCATTT[G/T]GTTCACCTCATTAAA | 51666 |
rs536102901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95512114 | GTAACACTTGATCCT[C/T]CCATGCTGTAGCCTA | 51666 |
rs536118462 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95521840 | TAAAAAGAACAAAAA[C/T]TTACCAAGCAATGAT | 51666 |
rs536158463 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95521898 | CTCTGTGGAGGAAAA[A/G]ATTATGGGAGAAAGA | 51666 |
rs536180651 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95524943 | GTTAACAGGAACCCC[G/T]CTTACTTTGCTGAGA | 51666 |
rs536198827 | snp | A/C | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95478245 | AAATTATGGTAAATT[A/C]TTCCCTCGAGTTGAT | 51666 |
rs536212519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471773 | TAGCAGGTTAATACC[A/G]GCTAACACCTCCAGA | 51666 |
rs536232759 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95520147 | TATCCCTGAGTCAAG[A/G]AATAATTTGAATTCT | 51666 |
rs536316347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95499336 | TCTAACATTTCAATG[C/T]TAGAAGGATGAGGAG | 51666 |
rs536358431 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95463159 | AAGCAATCCTCTTGC[C/T]TCAGTAGGGCCCACA | 51666 |
rs536389618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472743 | AGTATGATAAAACGC[A/G]GTTAACCTCAGCTGG | 51666 |
rs536404986 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95477754 | TTTTTTTTTTTTGCT[A/G]TAATTCTGTGATTCT | 51666 |
rs536446546 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95493546 | TCCCCTCTGGACAGA[G/T]AGACAATAGCTTATT | 51666 |
rs536475768 | snp | A/G | 0.000299058 | 0.0122245 | intron-variant, missense | ASB4 | GRCh38.p7 | 7:95528319 | GTGAGGCTCTGCCCA[A/G]TGGTCAGCAGGTTGA | 51666 |
rs536482343 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95535401 | AAAGGGGCTTTAGGA[G/T]GACCCCCTCAGAAAG | 51666 |
rs536497659 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95490456 | TAAAAAATAGCCAAG[A/C]ATTGTGCTTCAGTCT | 51666 |
rs536539889 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95537038 | TTGCTACCAATGTAT[A/G]CCAGTCCTTCCCACT | 51666 |
rs536575306 | snp | C/G/T | | | | | GRCh38.p7 | 7:95461803 | GTAATTGAATCATGG[C/G/T]GGTGATCCTCATGCT | 51666 |
rs536592573 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95470756 | TGGCTGGTTTCATAA[C/T]AGGACTTTTCAAGGC | 51666 |
rs536607520 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95480382 | CTAAGATGGACCCCA[C/T]TGATTCTCACTTCCT | 51666 |
rs536636425 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95522428 | TTATATCATTTAGGA[A/T]AATCTTTCCTAAATA | 51666 |
rs536663983 | snp | A/C | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:95479594 | TTTTGTGTGTTTGCC[A/C]CACTTTTTTGTGTTA | 51666 |
rs536698897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95516443 | TCTAGAAAGATATCC[C/T]TTCTTTAAGGTTGAG | 51666 |
rs536721502 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95514231 | CTGGGCTTCCTTGTT[C/G]ATTACTTGAATTTCT | 51666 |
rs536770108 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95531604 | TACTATTCTTAAACA[G/T]GTGTTGAGCAGGAGA | 51666 |
rs536807261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95491426 | TCCCCGGTTCTCCCT[C/T]ACCTCTGTCCTTTGT | 51666 |
rs536909102 | snp | C/T | 8.24817e-05 | 0.00642137 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95528216 | GCTGAAGGTCACCTC[C/T]GTGCGCCCTGCTGCC | 51666 |
rs536945120 | in-del | -/TT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513254 | TTTGTTTTTTGTTTG[-/TT]TTTTTTTTTTTTTTT | 51666 |
rs536983946 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484474 | GGTTTAACCTCAATG[C/T]TGATTACATGAGTTT | 51666 |
rs536993367 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95494908 | GTTCTAGGCACATCT[A/G]TGCTTCCCCTGCCCA | 51666 |
rs537009025 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95470658 | AAGCTGTGGTGTCAG[A/C]TCCTTTCTCATTTCC | 51666 |
rs537027038 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASB4 | GRCh38.p7 | 7:95513897 | ATCTGTCTGTCAATT[C/T]TGGTCCATTTCTCTA | 51666 |
rs537076908 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95536258 | TCTTGATGTGTTGCC[A/C]AAGATAGCTTTGAAC | 51666 |
rs537146736 | snp | A/T | 0.000399281 | 0.0141238 | nc-transcript-variant, intron-variant | LOC107986823 | GRCh38.p7 | 7:95471317 | TGCTATTGTCCTCTT[A/T]CCTGCACGCTTCCTC | 51666 |
rs537192714 | snp | C/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95479447 | GTCCACAGAATTGAT[C/G]TGTATTGTTATAAAA | 51666 |
rs537199582 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95483948 | ATTTCCATATATGGC[G/T]CTTTTTGTTGTTGCT | 51666 |
rs537263838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95490936 | TAAACTGCATGTAGC[C/T]TTCGGATCATAGACG | 51666 |
rs537381484 | snp | C/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95476818 | ACACATGGTATGAAA[C/G]ATTTTTAGCTTATTA | 51666 |
rs537401187 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95501301 | GGCAATGTAAAGGGG[A/G/T]CCATGCCTTTTAAAA | 51666 |
rs537430133 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95499589 | GAATGGTATAAAGTG[A/C]AAATGGGTGGTAAGA | 51666 |
rs537437933 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95494071 | TTTTGTGGAGTTGTG[C/T]AATACAGTGGTCCTT | 51666 |
rs537444716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95500794 | GTTATTTCTATGAAT[C/T]ACTTACTTTGGCACA | 51666 |
rs537455735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95493491 | GGATTAATCACTGTG[C/T]ACAACCTTGTAAATA | 51666 |
rs537470011 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95485399 | CTCCTCCCTTCCCAG[C/T]TTTTCATATTAAAAT | 51666 |
rs537495099 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95523383 | GCAAACAAAGCCGAA[A/C]GATTTCACCTAATAA | 51666 |
rs537501882 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95524775 | AAATGAGACAGCCAA[C/G]TATAATCGGGTCCCC | 51666 |
rs537504565 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95530435 | GTGCCACTGCACTTC[A/C]CCCTGGGTGACAGAG | 51666 |
rs537533144 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95480223 | GTAGCACATATTACC[A/G]TGTGACAAACTATAT | 51666 |
rs537577946 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95494629 | CATCTTCTTGCCCTC[A/G]GTATTTTTTCTTTCT | 51666 |
rs537617330 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95463482 | GGAGGTGATTGGTTC[A/G]TGGGAGCAGTTTCTA | 51666 |
rs537617413 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472526 | CTGTGGAACTGCAGT[G/T]CTATAAATCTGCAGT | 51666 |
rs537629243 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95499283 | GGATAAAGAGTATAT[A/T]TAGAGAAAAGTGAAT | 51666 |
rs537772206 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95506468 | CCTCTGGTACATTTC[G/T]GAGAAAGGGTGCATG | 51666 |
rs537825775 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95518640 | ATACCTAGATAAGGG[A/T]AAGATAGAGATTAAA | 51666 |
rs537835880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95501517 | TCATAAATAAGAACA[C/T]TTAAGATCTACTTTC | 51666 |
rs537848014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95508935 | GATATGTGAATCAGT[A/G]ATTTCTGGAGACAGA | 51666 |
rs537887391 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95517921 | TAGAAAATGAGGGCA[A/G]AGAGTCCATGGGAAT | 51666 |
rs537929269 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | ASB4 | GRCh38.p7 | 7:95533758 | ATGGGGATGAATATA[-/G]GGACCAACCTCATAG | 51666 |
rs538009755 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95481032 | TCAAGATCTAGGCTT[C/G]AGTGTTATATCTGCT | 51666 |
rs538026563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95516321 | TATCTATGGTTACTT[C/T]GCAAAATTTTAATCA | 51666 |
rs538064011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95487845 | ACAGTTCCATTCTTA[C/T]GTATGCCAAGTGGAT | 51666 |
rs538076035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95523908 | CGTGTCTAACTTCAT[C/T]GGTAATTAGGGAAAC | 51666 |
rs538079375 | in-del | -/A | | | intron-variant | ASB4 | GRCh38.p7 | 7:95502031 | ATCATAAAACTGGGG[-/A]AAATATTTGAGACTA | 51666 |
rs538081155 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95531988 | AGTTGGCTACTGGTA[G/T]ATGGCTGGTATTACA | 51666 |
rs538197094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473591 | TGCAACCTGAAAGAG[C/T]CTATAGAATACAGAT | 51666 |
rs538209437 | snp | A/T | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:95466633 | AAAAGAAGACATTTT[A/T]TGTTTATTGCCAGTG | 51666 |
rs538238608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95500000 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGAGCATC | 51666 |
rs538239054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95508003 | GAACAAGCCTTTTAA[A/G]GAGTATTTGTGAAGA | 51666 |
rs538251169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95507550 | ATTTTATTTGTTGAA[C/T]TCTTTGATTAGTAAC | 51666 |
rs538311515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95511241 | CAAAACATTTTGTTG[A/G]CAGCCCGCCCCTACC | 51666 |
rs538334179 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95459612 | AGCAGGGCAGAATAC[A/G]ATGCTCTGCCCACTG | 51666 |
rs538346456 | snp | A/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95467323 | GTGACCCTGAGAAAG[A/T]TACTTAATTTCCGAA | 51666 |
rs538388292 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538129 | ATCAGTAATATGTTT[A/G]CATTCTCATTCAAAT | 51666 |
rs538512514 | snp | C/T | 0.000798403 | 0.0199641 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95474173 | CTGACTTCAAATTAG[C/T]GAATATGCATATGTG | 51666 |
rs538544174 | snp | C/T | 0.00159617 | 0.0282053 | | | GRCh38.p7 | 7:95463388 | CTGGAGGATCTGTGA[C/T]TGCTATGGTTTGAAT | 51666 |
rs538572557 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95481618 | GCTTAGTAGCATCAA[A/G]TTCATGTTTAAATGC | 51666 |
rs538600745 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95463989 | GGATTTTAACTAAAG[C/T]GGAAAAGATGCCCTA | 51666 |
rs538629905 | snp | C/T | | | | | GRCh38.p7 | 7:95482910 | ATGCCTGAGGAAGTT[C/T]GAGGACACTGAGGTT | 51666 |
rs538631540 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95525182 | GGTCTGAGGCAGATT[C/T]TCCTCCAAAGTCTCT | 51666 |
rs538640680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95517314 | GCTGGGACTACAGAC[A/G]TTAGCCACCATGCCA | 51666 |
rs538724055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95509262 | TTATTTATCTTTCCA[C/T]GAGAATTAGGGAGTA | 51666 |
rs538787748 | snp | C/G | 0.00318978 | 0.0398085 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471406 | GATCAAGAGTGGTTG[C/G]TTCAGGGACCTTCCA | 51666 |
rs538811398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95486838 | CAAAAATTAGACCAA[C/T]TTTTTTTTACCAAGG | 51666 |
rs538847541 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485724 | TATCACGGGGGCTTT[C/T]GTTCATATTGACACT | 51666 |
rs538871171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95522635 | GCACTTATCTGTGTT[A/G]GTCCTCCCGTTTAGT | 51666 |
rs538879777 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95529663 | TATATGTAAAGCCCA[C/G]AATGTCATGAATTTT | 51666 |
rs538906891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95531893 | AACCAACTTTGTCCA[C/T]GGTTAGCATTTTCTT | 51666 |
rs538955555 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95488295 | GCAGTGAGCCCAGAT[A/G]GCGCCACTGCACTCC | 51666 |
rs538970755 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95530847 | TGAGTGGGGGGCTGG[A/C]AAATTTGCAATAATT | 51666 |
rs539081635 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95534801 | GTCATAAATCTCCCA[A/G]AATTACTGTCATAGT | 51666 |
rs539093848 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95517842 | GAGTTCAAACAAAAA[A/G]CAATAGAAAGAAATT | 51666 |
rs539116910 | snp | C/G | | | downstream-variant-500B | LOC107986823 | GRCh38.p7 | 7:95474717 | TTTTTTTAGAGATGG[C/G]TGTCACCATGTTGTC | 51666 |
rs539124651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95533645 | TGTTTTTTTGACTTT[A/G]GAGTCATGCAGACTT | 51666 |
rs539138439 | snp | A/C | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95483014 | GCCCTAAGAAGATGG[A/C]ACAATAGAAGATGAC | 51666 |
rs539184431 | snp | A/C/G | 0.000798403 | 0.0199641 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95474048 | GATCTTTTCTGTAAA[A/C/G]CTAGATTTTTATGTG | 51666 |
rs539253594 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95533217 | AAATTCAGTTTGGGG[G/T]TAGAATGTTAGAAGC | 51666 |
rs539343126 | snp | G/T | 1.75748e-05 | 0.00296431 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95537810 | TAAGTGGACTTGCTG[G/T]GTAGACACAGTTTGC | 51666 |
rs539349874 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538553 | GCTTATCTTTCAAAG[C/T]TGTGTTTCTGACATG | 51666 |
rs539359532 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95487762 | AGGTGTTTTCATAGT[G/T]TTAGGACTGTGGGAT | 51666 |
rs539379475 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95480471 | CCATAGGATATGATA[A/G]AAACAGTGGTATATG | 51666 |
rs539389492 | snp | C/T | | | | | GRCh38.p7 | 7:95464107 | AAAAAATCATTCTGA[C/T]AGGTTTCCAACAGTC | 51666 |
rs539392477 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95488055 | CTTTCTTAAAAGTTT[C/T]TTCAGGCCGGGAGTG | 51666 |
rs539435635 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515875 | TCAAAAAAGTAGGCT[C/T]ACTGTTGCTTGACAA | 51666 |
rs539436192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95497069 | ACAAGAGGGTAGAGG[A/G]GAGTGTTACAAGATG | 51666 |
rs539439767 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95504980 | TTCAGGAAACACAAC[A/C]TTAAGCAGTGCTTTC | 51666 |
rs539450237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95504153 | TCTACCTATTCCATT[C/T]GTAAGAGGAAAATGA | 51666 |
rs539452116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95512734 | AAGAATGAAATTAGG[A/G]CCTATAGCTAGAAGG | 51666 |
rs539455451 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538919 | GGCTACGAAAAGTAA[A/G]TAGAGAGACTTTTTG | 51666 |
rs539458950 | snp | A/C/T | 0.000296792 | 0.0121783 | missense | ASB4 | GRCh38.p7 | 7:95495896 | GACCCAATGGGAAAA[A/C/T]CCCTCTTCACGTGGC | 51666 |
rs539502539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95525888 | TTACAGAGCAATGTA[C/T]TCTTGGGTACCTTCC | 51666 |
rs539525683 | snp | A/C | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473307 | GGGCTTTACACATGT[A/C]AACTTAGTTAATCCT | 51666 |
rs539609453 | snp | A/G | 0.00159617 | 0.0282053 | | | GRCh38.p7 | 7:95475581 | TAGAGATGGGGTTTC[A/G]CCATGTTGGCCAGGC | 51666 |
rs539623278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95510194 | GATATGAAAAACTGT[C/T]GATGTTTCTTCCGAA | 51666 |
rs539634550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95502322 | ATACAAAAGATAATA[C/T]ATATATGACAAACAC | 51666 |
rs539744745 | snp | A/C | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95468412 | ACTAATTCAGTAAAA[A/C]GTATGTAAAACCACT | 51666 |
rs539772480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95503049 | GGACTGTATAGATGT[A/G]TTTTTCTGAAAATTA | 51666 |
rs539774264 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95495233 | AAAATCTTGGAGTGA[A/T]AATTTTTTTAAAAAG | 51666 |
rs539837556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95487999 | CGCACATGGGCACAA[A/G]GACCTGTCTCTTTAG | 51666 |
rs539850072 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95487192 | AGTTCTGAGGGACAT[A/G]TAGAAGAGCTCAGGC | 51666 |
rs539912502 | snp | C/G | 0.00119737 | 0.0244387 | downstream-variant-500B, intron-variant | ASB4 | GRCh38.p7 | 7:95540314 | CTGAAGAACTCTACA[C/G]ATTTCATTGCTTTTA | 51666 |
rs539973442 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95524181 | CCAGAGTACAAGAAT[G/T]TGCAAGAATGCCCAT | 51666 |
rs539991855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473029 | CAGTGGCAAGTTTCC[A/G]TGGAGTCGGTAGCTC | 51666 |
rs540009396 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95519959 | TTTTGAATATGAACA[A/G]TGTTTCAAAACAGAG | 51666 |
rs540017553 | snp | A/G | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472728 | AGGGAGCTTCTTTGC[A/G]GTATGATAAAACGCG | 51666 |
rs540026938 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95512333 | AAATGGGGCTACGGA[C/T]AATTCAAGTTGATTC | 51666 |
rs540090621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95512003 | TCCACTGTAGACTGT[A/G]TATGTCAGTCAGCAA | 51666 |
rs540096422 | in-del | -/GTG | | | intron-variant | ASB4 | GRCh38.p7 | 7:95527221 | CATGCACAGGCATAT[-/GTG]GTGGTGGTGGTGCTG | 51666 |
rs540098046 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95500048 | GGACAAAGTAAAAGA[A/T]GGTTTTAAATGCCAG | 51666 |
rs540107574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95486543 | TGGTTTAAGAACACG[C/T]TGCTAATTCTCCATT | 51666 |
rs540291550 | in-del | -/A | | | intron-variant | ASB4 | GRCh38.p7 | 7:95488863 | GAATCTTCAGGTTTC[-/A]GTTATTTTTGGCTTA | 51666 |
rs540324665 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95532798 | CTCTCTTCAGTAGTC[A/G]CCACAGTAGAAATAA | 51666 |
rs540331808 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95508252 | AGGAGAACCTCTGTT[C/G]TATCGTAGCCAGAGG | 51666 |
rs540403398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95500993 | CTCTTCACATTTACT[C/T]ATTCATTTATGTTTA | 51666 |
rs540408831 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95509574 | CTTGAGTAAATAATT[A/T]AATATCTTTGTGCGT | 51666 |
rs540451622 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95518029 | GAGGAAGGTGTTGGT[C/G]TTAAATTGGAGGAGA | 51666 |
rs540492500 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95464882 | AATATCTCAATTTCT[A/G]CAAACTAGGGAAAGG | 51666 |
rs540493395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95510670 | TGATTCCCAAGTGCT[C/T]CAGAGGAAAAGTAGT | 51666 |
rs540495505 | snp | A/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538496 | AGCTAACTGCAATAT[A/T]AAGTGATGGGGCAAG | 51666 |
rs540521279 | snp | C/T | 0.00199481 | 0.0315187 | | | GRCh38.p7 | 7:95479160 | AGGAAAAGAAGTCAC[C/T]GAGAGGTATTTTGAA | 51666 |
rs540527734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95537408 | TCCTTGTATACCACC[A/G]CCTCACTGCTCCCAT | 51666 |
rs540540923 | in-del | -/A | 0.00159617 | 0.0282053 | | | GRCh38.p7 | 7:95478738 | TGCCAGGCCACAAAT[-/A]AGAGTTCCAAGCGAA | 51666 |
rs540541709 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95536684 | ATGCAATGAGACAAA[A/G]GGTTATAAAATGCAG | 51666 |
rs540587439 | snp | C/G | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95485424 | TAAAATTTTTCAAGT[C/G]TAGGTCACTTGAAAA | 51666 |
rs540632277 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95468806 | AATAAGTAGCATCCA[C/T]TTTCTGCATCTCATT | 51666 |
rs540817138 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95460443 | TATGGACAATGAAGT[C/T]CAGGCTGAGGTGGCC | 51666 |
rs540845624 | snp | A/G | 0.000399281 | 0.0141238 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95473720 | AGGATTGAAGAAGCG[A/G]TTCCTGTTTTTGAGG | 51666 |
rs540860541 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95533382 | TTCTAACACTCTTCG[A/T]GCTGTGACACCAAGG | 51666 |
rs540866104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95517587 | AGGGAGAAGAAAGCA[C/T]ACCCAAGGAAACTGA | 51666 |
rs540901131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95525614 | TTGTTCCAAGTTGGC[C/T]TGTAAGAATTTCATC | 51666 |
rs540979141 | snp | C/T | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:95477116 | TTGGATTTTTTTTTT[C/T]TCCCCAGGATACTGC | 51666 |
rs540982603 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95459806 | TCGGTGACTACTGGT[A/G]TTTCTAGATTGTGGC | 51666 |
rs541031032 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95535085 | ACATGCACACACATG[C/T]GCACACTCTTACTTA | 51666 |
rs541033075 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95509110 | CCCAAAATAATGTCA[A/G]GAATTTTTGAGGTGA | 51666 |
rs541069596 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | ASB4 | GRCh38.p7 | 7:95511675 | CTCAAAAAAAAAAAA[A/T]AAATAAATAAAAATA | 51666 |
rs541096211 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95504446 | TAGATATGCCTGCTG[C/G]ACAGACGCTGCTCTT | 51666 |
rs541125766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95521976 | AAACTAAAGCAAATA[C/T]GGTAATAATTAAATT | 51666 |
rs541133955 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95501939 | CAAAGGCCGAATTCA[C/T]AAAGAAAATAGAGAT | 51666 |
rs541149952 | snp | C/G | | | | | GRCh38.p7 | 7:95479542 | CAAGATGGCCTCTGG[C/G]AATAGATCATTGAAA | 51666 |
rs541167996 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95533784 | CATAGGATTGTTCAA[C/T]GGCTGAGCAAGTTAA | 51666 |
rs541195883 | snp | G/T | | | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95473748 | AGGCATTTGCAATCA[G/T]TGCTGGAGAGACAGA | 51666 |
rs541225010 | snp | A/G | 0.00159617 | 0.0282053 | | | GRCh38.p7 | 7:95482679 | CTCTGGAGGGAGATC[A/G]ATAGGCTTGCTGACG | 51666 |
rs541225257 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | LOC107986823 | GRCh38.p7 | 7:95474577 | TCCAGGCTGGAGTGC[A/C]GTGGTGCAATCACGG | 51666 |
rs541237436 | snp | A/G | 0.00199481 | 0.0315187 | | | GRCh38.p7 | 7:95482113 | ATTTGCTTTGTAGGT[A/G]CAAATAATCTGTAAG | 51666 |
rs541256414 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95497933 | CTACCCCCCAGTAGA[A/G]GGACATTTGGAATGT | 51666 |
rs541314580 | in-del | -/TTTA | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95510879 | TTAGGCCTGTACTTC[-/TTTA]TTTATTTTCTATCAG | 51666 |
rs541372737 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ASB4 | GRCh38.p7 | 7:95540554 | TTCCTTCATTCTCAC[C/T]GTCCACTAAACCCTG | 51666 |
rs541381842 | snp | A/G | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:95466892 | CATGAGAACAGCATG[A/G]AAAAACCTGCACCCA | 51666 |
rs541389129 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASB4 | GRCh38.p7 | 7:95490953 | TCGGATCATAGACGG[C/T]TATTTAAAGATTTGG | 51666 |
rs541396176 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95516356 | TTTTTTGGAATTAAA[A/G]AGATAAAAAATAAAA | 51666 |
rs541400186 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484585 | TAAAATTATGTTGTG[A/G]TTTGCATCATTTACA | 51666 |
rs541407000 | snp | C/T | | | | | GRCh38.p7 | 7:95476032 | CTTGATTCCTCAAAC[C/T]GAATGGTGTGATCTT | 51666 |
rs541419594 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95475060 | CAAGCTGTTTTTTAT[G/T]TATAGTGCCTAGACC | 51666 |
rs541431160 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95506517 | AGTGCATGAATTCTA[C/T]CCCCGACTTAGAGTA | 51666 |
rs541473204 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95527619 | GTTGTCCAGGAGATG[G/T]CACTGTTGCTTCAAG | 51666 |
rs541506449 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95459793 | GGGCTATTTTCTGTC[A/G]GTGACTACTGGTGTT | 51666 |
rs541537116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95521281 | ACCCAATGAAAAATG[A/G]GCAGAAGCTATGAAG | 51666 |
rs541553413 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469853 | TTATATCAGTCTTAT[C/T]AGATTGATGTAAGAA | 51666 |
rs541559039 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | ASB4 | GRCh38.p7 | 7:95528436 | CCTCTTTGACCTTCC[A/G]TTACATACCTAATCC | 51666 |
rs541587037 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95540107 | GTGCTTAAACACTTA[C/T]GTTCATCTAGTGTAG | 51666 |
rs541592516 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538634 | AAAGTAGAGGGATCT[C/T]CTGCTCTTGTTAGGG | 51666 |
rs541605169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95490682 | TACATCCTCTCCAAA[C/T]GCTGGAGCAGAACCA | 51666 |
rs541617349 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95497401 | CAGAGATGGATTGGA[G/T]GTGGGTGGGGTGTGA | 51666 |
rs541744005 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95534616 | CCACTCTCTGCCCTC[C/G]ATGCACTTGTCTTCT | 51666 |
rs541765328 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95526028 | TACATGGTAAACGGA[-/T]TTTTTTTTAAAGCTA | 51666 |
rs541831092 | snp | A/G | 0.000399281 | 0.0141238 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95474475 | GACAACTGGACACCT[A/G]GTTATGATTGCAGAA | 51666 |
rs541861675 | snp | A/G | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469253 | CATGCAGACAATTTT[A/G]TCTTGTGAGTTCTGG | 51666 |
rs541876572 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95518282 | GAACAAAAGAAATAA[C/G]AGTGGCTTCCAGGCT | 51666 |
rs541905455 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95511634 | GCCATTGCACTCCAG[C/G]CTGGGCAACAAGAGC | 51666 |
rs541912517 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95520443 | TCTGTTGTTTCAGAT[A/C]TCATAGAAGGCTTGG | 51666 |
rs541961128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95534516 | ATACTTGTTTCTTCT[C/T]CCAGCTTCAGCCACC | 51666 |
rs541966721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95510900 | TATTTTCTATCAGCA[C/T]TTTAATTTGTTTCTT | 51666 |
rs542008569 | snp | A/G | | | | | GRCh38.p7 | 7:95466007 | GAATAGTGCAATTTA[A/G]GTATGATAATAAGCT | 51666 |
rs542044063 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95489005 | GAAAAGTAGTACAAT[C/G]AATTCTAAACCATTC | 51666 |
rs542056422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95495304 | AAAAAAGATTTTGGA[C/T]AGAATAAAAATTATA | 51666 |
rs542174491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95533969 | CACTGAACTTCATGG[C/T]TTCTGCCAGCACATA | 51666 |
rs542304867 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95506305 | GACCTGCTCCAATGA[A/G]TTTCAGGTTGATGTG | 51666 |
rs542311881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95535287 | CAGTAATAGGTTGAG[A/G]TTGATACGGTCTGGG | 51666 |
rs542392118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95496517 | TGTATAAAGTCTTCT[C/T]TAAGGATATTATGCT | 51666 |
rs542455489 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95503499 | GGATGGGGACCCACT[C/G]CCACCTAATAAATGA | 51666 |
rs542476561 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95477014 | AGGAAAATATGATCA[G/T]GAAAGATATGGTTTA | 51666 |
rs542549871 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539477 | AATAGAATGCTGAAT[C/T]TGTATGAATTATTCA | 51666 |
rs542652134 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95498259 | GAGAACTGCTTGGGT[C/T]TAGGAGTTTGAGTTC | 51666 |
rs542674401 | snp | C/T | | | | | GRCh38.p7 | 7:95483143 | GGACCAAGTAAGTGA[C/T]GACCCATTCTGCCAC | 51666 |
rs542734147 | snp | G/T | | | utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485962 | CAAAGCTTCCAGAGG[G/T]AGAGGAAGGATGGAC | 51666 |
rs542828302 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95468945 | TTTTTGAACATGTTG[C/T]ACAATCATACTTTCC | 51666 |
rs542846178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95535785 | AAAGGTAAAATACCA[A/G]TAAGTGTGGTTTAGT | 51666 |
rs542925416 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95462097 | ACTAATATAGTGGCC[C/T]TCTCTAGCACCCAGG | 51666 |
rs542988054 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95478866 | GCTCCCAGTATGTAA[C/T]TACAATTGAGAATGA | 51666 |
rs543026887 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95505472 | CAAGGTTTATAATGA[A/G]AAATGTAGTACTAGA | 51666 |
rs543038528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95523474 | ACAGAGAAAGTGTCT[A/G]AACTCTAATAATCAA | 51666 |
rs543100924 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95507768 | TCATGCTCAGTTGTA[C/T]ACATTGCTTCTTTCC | 51666 |
rs543161274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95515626 | TCCCCATGTTGACCA[C/G]GATGGTCTCAATCTC | 51666 |
rs543163185 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95507226 | TTATGAATTTTTTTT[A/T]CCTTGAGATTGGTCA | 51666 |
rs543240237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95526843 | TAGAGTTGGCCCCCT[A/G]AGGGTCATTTGGTTC | 51666 |
rs543249417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95492852 | GAGTATTAAAATGAC[C/T]GATTAAGTATTGAAG | 51666 |
rs543261994 | snp | G/T | 0.00358779 | 0.0422022 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95470914 | ACATAATAACTCTCC[G/T]GGTGGTTCCCTGTTT | 51666 |
rs543319604 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95526139 | AGAAAAGTAATATGA[A/G]GTGGAATAGAACAGT | 51666 |
rs543453779 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95504556 | CAAACCACCCTGAGG[A/T]TTTTTGCCACATCTG | 51666 |
rs543468488 | snp | A/C | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95477943 | TTTTCCTGCAATATC[A/C]CATAGTTTTGGTGTT | 51666 |
rs543491201 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95462753 | TTAGCATTTGAATAA[C/T]TAAAACTGGGATTAT | 51666 |
rs543552825 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95462352 | CAGCCCCCTTTGTAA[C/T]AGCTTTTTCCTATTT | 51666 |
rs543597216 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95475960 | TGAACTTTTCGGTCT[C/G]TATATATCAAGATCC | 51666 |
rs543664913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95512349 | AATTCAAGTTGATTC[C/T]AGGGAACTCCAGCAA | 51666 |
rs543681350 | snp | A/G | 0.00159617 | 0.0282053 | | | GRCh38.p7 | 7:95460473 | CTCAGGTGGAGATGA[A/G]GAACTTGGGAACTGA | 51666 |
rs543725535 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95508399 | AAGAAGTATAAAAGA[C/T]CTGAGGAAAAAAGAG | 51666 |
rs543761448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95535197 | AAAAGGCAATGCTAG[A/G]CCACCTATGAGGAAG | 51666 |
rs543781150 | snp | A/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95468909 | TTCTTTAAAAATTTT[A/T]AAAAATCAGTGCTCT | 51666 |
rs543826717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95529227 | AGCTAGTAATTAATT[C/T]GGAGGCCAAAATGCA | 51666 |
rs543925576 | snp | C/T | | | | | GRCh38.p7 | 7:95465802 | GCAGTGGCACTTACC[C/T]GTAGTCCTAGCTACT | 51666 |
rs543930040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95486940 | ACTGGTTAATTGGGG[A/G]AACGTGAGTAGTTAG | 51666 |
rs543930843 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95527663 | CGAGGCCCAGGAAGA[A/G/T]AGCCTGGGGGCAAAG | 51666 |
rs543946687 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95522673 | TCTTTCCACACAAAG[C/G]CTTTTCAAGAAATCA | 51666 |
rs543986276 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484144 | ATCAGCCGGGGGAAC[A/G]TGGCAAAACCCTGTC | 51666 |
rs544009243 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95479979 | CTAAATATCAGCATA[A/G]CTTATTCCCGCAATT | 51666 |
rs544020297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95491912 | TTTCCTGATATGCTC[A/G]GGGCTGAATTATTCA | 51666 |
rs544073878 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95493162 | TATTAGAATTTAATT[A/C]TATTAGCTGAATATA | 51666 |
rs544090683 | snp | C/G | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473390 | CCAAGGCACAGAGAG[C/G]GTAAGCAGTTAAGTC | 51666 |
rs544099785 | in-del | -/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95495752 | CCTTTTTTTTTTTTT[-/T]CAGGTTACTGGTTGC | 51666 |
rs544116609 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ASB4 | GRCh38.p7 | 7:95528548 | AATTTGTTTTGCCTT[C/G]TGTGAACACCAGTGC | 51666 |
rs544126278 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95507136 | CTACGTAGAGGTTTT[C/T]TGTTTGTTTGTTTGT | 51666 |
rs544361571 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95495208 | TGCATAAATCAACAG[A/G]CAGGCAAATAAAATC | 51666 |
rs544430450 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95524137 | CCACTCATAGATGTA[A/G]AGCCCAGAGAAATCC | 51666 |
rs544468638 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95500031 | CTCATTTTTAAGAAG[C/T]GGGACAAAGTAAAAG | 51666 |
rs544539206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95508568 | GAGTTTTGATGTTTG[C/T]CTTTATGATGCTACT | 51666 |
rs544613139 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95520797 | GGTCTGTTTCTAGGC[G/T]TTACGTTCTATTTCA | 51666 |
rs544672244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95492950 | AGAGATTCAATGTAC[A/G]TAACTCAATAGAAAT | 51666 |
rs544702211 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95529470 | GGCTTAGTTAGAAGA[A/C]AAGTTCTACTAGAGA | 51666 |
rs544714626 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95535978 | CCAGGCAGCTGGGAA[C/T]GTATTCTGTGTCCAG | 51666 |
rs544748298 | snp | A/C | | | | | GRCh38.p7 | 7:95464526 | GTAATTATTAATTAG[A/C]AAACTACTCTTTCAT | 51666 |
rs544783424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95506538 | ACTTAGAGTAGAATT[C/T]TAGATTCATAAACAT | 51666 |
rs544801705 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485473 | ATATGTATGACAATG[G/T]TTGATTTTACAAGCT | 51666 |
rs544807003 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95480553 | GGATCTTTCATTCTG[A/G]GAGAAATCAGTTACC | 51666 |
rs544840313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472311 | CCCTGTGTTCAGAAT[A/G]ACCAGATGCTTAGAC | 51666 |
rs544864494 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95517776 | TGATGGACTGAGGAG[A/T]GTATCGGTGGTGAGA | 51666 |
rs544870229 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95507105 | GTCACTAAAAGCTGA[C/T]TTGGAATCTAATTAT | 51666 |
rs544871858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95498804 | TAGGTGTAGGATTCA[C/T]TTTGAGTTAATTTTT | 51666 |
rs544902578 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95465950 | TCTGAAACAAACAAA[C/T]AAACAAACAAAAAGA | 51666 |
rs544915630 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95513975 | GTCCAAAATCACCCT[C/G]ACAACTCCTGGACCT | 51666 |
rs544964006 | snp | A/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95464720 | ATTTTGTTACAGTTA[A/T]CCTTTTTCCCCATGA | 51666 |
rs545062459 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95535329 | AAATGTCTTTGGAGA[A/C]AGTTGTTTAAGTGCA | 51666 |
rs545117617 | in-del | -/AG | 0.0023933 | 0.0345097 | intron-variant | ASB4 | GRCh38.p7 | 7:95494821 | GATCAGTGGGAGAAA[-/AG]AGAGAGAGAGAGGCA | 51666 |
rs545172409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95514555 | ATGTTCAGTGTCTGG[C/T]TTCAGGGTACACAAA | 51666 |
rs545282064 | in-del | -/A | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95485435 | AGTCTAGGTCACTTG[-/A]AAAACCTCCTGTTTG | 51666 |
rs545284576 | snp | A/C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95533948 | ATTTATACCCATTTA[A/C/G]ACTGTCACTGAACTT | 51666 |
rs545352484 | snp | C/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95463638 | CTCACTTCCCCTTCC[C/T]CCTCCACCATGATTG | 51666 |
rs545399984 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95523563 | TATACTGCTTAGTGA[C/G]GTAATTAGTCTTATG | 51666 |
rs545431825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95516548 | CAATATTCTGTGGAG[C/T]TGGCAGATAAGCTTT | 51666 |
rs545445661 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95536035 | TACAAAGGCAAAGTA[A/G]TTCTTCAATTCTCAT | 51666 |
rs545482940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95501120 | TTAATTTAATCATTA[A/G]CTTTCTAATTAAAAC | 51666 |
rs545548483 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASB4 | GRCh38.p7 | 7:95495098 | TTTTTATTTTCCTAC[C/T]TTTTTATTTTGCCCT | 51666 |
rs545570752 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95479793 | GTTCAAGAAGTAGAA[A/G]AAAGGAAATAAATGC | 51666 |
rs545600021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95486267 | GTTTCTTTAAGTATT[C/T]ATTTAAAAAATATTT | 51666 |
rs545604475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95517659 | AGATATAGTAGAGAG[A/G]TGTGGTAACTGGAAG | 51666 |
rs545618848 | snp | A/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95466152 | CTTTTTATATAATTC[A/T]TACAACAATCTCATG | 51666 |
rs545645296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95537493 | TTACGTATAGAGGTT[A/G]GTTGCAGCATTGCTG | 51666 |
rs545667697 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95487336 | GGTCTGTTAGAAAAT[C/T]TGTATACTATATAAT | 51666 |
rs545684604 | in-del | -/C | 0.00597247 | 0.0543191 | | | GRCh38.p7 | 7:95461493 | TACCCAATGCCTATA[-/C]CCCCATTGTATCTAG | 51666 |
rs545756587 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472099 | TGGGAGGGGACTTAC[A/G]ATATCAATAATGACA | 51666 |
rs545792961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95496468 | AGAAAACAGGAGTTA[C/T]GAATGAGGATGTCAG | 51666 |
rs545796228 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95481360 | AGAATAGCAAAAAAA[A/G]GAAAAAAAAACAACA | 51666 |
rs545844977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95518155 | AGCAATGGTAGAAAT[A/G]ACTAGTTTTCACCAA | 51666 |
rs545852058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95524865 | CCGTTTGCAGTGGGG[A/G]GCAGCCTGGCCTCTC | 51666 |
rs545938294 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ASB4 | GRCh38.p7 | 7:95525446 | AAATAATTGTACTTT[A/C]TATATTTCCTGGAAA | 51666 |
rs545963555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95502601 | TGGGGAGAAAGAAAA[A/G]GAAAGACACTGATCA | 51666 |
rs545984440 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539988 | TATTCTAGCAGCAAA[G/T]CTTGTGATGCACTGA | 51666 |
rs546006888 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95490386 | TTACACTTCAAACTT[C/G]CTTTTATCCCCCCTT | 51666 |
rs546013608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95494731 | TTTATAAAGTCATCA[C/T]AGTTATAGCTTGTCA | 51666 |
rs546025741 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95501845 | TTGTAGGCTGACACT[A/G]ATGAATTAGGCTTAT | 51666 |
rs546087938 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538050 | TTTTTGTAAAACTTC[G/T]TATATCTTATCTCAT | 51666 |
rs546104739 | snp | A/G | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539972 | CCTGCATCTTAAGGC[A/G]TATTCTAGCAGCAAA | 51666 |
rs546110319 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95531146 | TGGTGCCAAACATTT[A/C]TTTCCTCTTTCTCTT | 51666 |
rs546143021 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539269 | ATATTCCAATAGGCT[A/T]TCATTTAATGTTAAC | 51666 |
rs546199168 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95480144 | GCACACCTTGTTCTG[A/G]TCTATACAAGGGTGG | 51666 |
rs546199476 | snp | A/T | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95470167 | TCTCCCAAATTACAG[A/T]TATACAGTTTCAGAG | 51666 |
rs546222848 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95515400 | TCTTTTTTTTCTTTT[C/G]TTTTCTTTTTCCTTT | 51666 |
rs546243204 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95507947 | TGCAGAAGTCAGAGT[C/G]GGGGGGATTGAGAAC | 51666 |
rs546476849 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95497917 | ACATAACAAAATTGA[C/T]CTACCCCCCAGTAGA | 51666 |
rs546502191 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95507070 | TAATCCTTGGCTGTC[G/T]GCCTATATTTAAGAT | 51666 |
rs546564039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95531693 | GTGTGTGAGTCCCTG[C/T]CCAGAGACTAAATGT | 51666 |
rs546573509 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472427 | CAAATTATGTACCTG[A/G]TCCTGTGTGGAATTC | 51666 |
rs546608640 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95523737 | AATTGTAGCATTAAT[A/T]TTAAGATCAAAATTT | 51666 |
rs546700981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95532251 | TTATTTACAAGGAAC[A/G]AGGTCAGAGCTGAAG | 51666 |
rs546712604 | snp | C/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95463889 | CATCTGTTAGAATAA[C/T]TACTATAAGTTATCA | 51666 |
rs546734150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95534430 | CAATCAGTGGCAACT[C/T]TTGTTTGTCCTCTAT | 51666 |
rs546787979 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95524537 | TTATATACTATGTAA[C/G]GTATGTTATGTGTTA | 51666 |
rs546818241 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95493246 | TCAGTCCATTAGACC[G/T]TAATGTGAAATAACT | 51666 |
rs546825622 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95519096 | CTGAAAGGAAATGGT[A/G]CTTCATTTAAGATTT | 51666 |
rs546859498 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95493961 | TAACCATTCGAACAA[C/T]GCTGTAGTGTAGTGC | 51666 |
rs546859750 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513449 | AGGGAATAGATACAG[C/T]CTGTTGCCAGAGCCC | 51666 |
rs546867225 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95530203 | CAGTGGCTCACCCCT[A/G]TAATCCTAGCACTTT | 51666 |
rs546930769 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95531899 | CTTTGTCCATGGTTA[A/G]CATTTTCTTATTCAG | 51666 |
rs547006060 | snp | A/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95480905 | TTGAATGAAGGGCTA[A/T]ATGTGAGCTGATTTC | 51666 |
rs547020455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95487744 | TTTCATTCCCACGAA[C/T]TGAGGTGTTTTCATA | 51666 |
rs547068519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95525163 | CACCAGAAGGTAGGA[A/G]AGAGGTCTGAGGCAG | 51666 |
rs547144403 | snp | G/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95481519 | CAGGAGGCCCAAGGG[G/T]TTCTGTTGCCACAGA | 51666 |
rs547145417 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95496631 | GTGAGAGGATCACTT[A/G]AGCCCAGGAGTTCGA | 51666 |
rs547145791 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95503400 | CAGCTTCTTGGACAG[C/T]GCTTGGCACATAGAA | 51666 |
rs547148697 | snp | A/C | | | missense | ASB4 | GRCh38.p7 | 7:95495883 | ACAATCAACTGTAGA[A/C]CCAATGGGAAAACCC | 51666 |
rs547161928 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539607 | TGGAGCTGGAGGCCA[C/T]TATTCTAAGTGAAGT | 51666 |
rs547187515 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASB4 | GRCh38.p7 | 7:95509933 | TATTTGTTTTGGGTC[C/G]GTGATGCTCCCACTG | 51666 |
rs547237676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95494346 | ACTTCTCTTGTTCTG[A/G]ACACTACACTTTTAT | 51666 |
rs547375420 | in-del | -/T | | | | | GRCh38.p7 | 7:95478125 | AAAAGGGAAGGATAA[-/T]TTTTTTTTCTTACTG | 51666 |
rs547457924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95503036 | TATGGGACAGTATGG[A/G]CTGTATAGATGTATT | 51666 |
rs547500387 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95533234 | AGAATGTTAGAAGCT[G/T]TGTATGGCCCCCTAA | 51666 |
rs547520129 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95466513 | AATTTTTATGGAATC[C/T]AAAAACAACAGTGAA | 51666 |
rs547584288 | snp | A/G | 0.000399281 | 0.0141238 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95473986 | ACTGAAAATAAAGCC[A/G]TAAGTTACCTCCAGA | 51666 |
rs547585869 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95482359 | AAATTTTAAATTTGC[A/G]TCCAGATATTAAAGC | 51666 |
rs547614573 | snp | C/T | 0.00199481 | 0.0315187 | | | GRCh38.p7 | 7:95460877 | TGTGTCCAGGGCCCC[C/T]GTGCTCTGTGCAGCC | 51666 |
rs547623890 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95517901 | TGCAAAAGCTTAAGT[A/G]TGCTTAGAAAATGAG | 51666 |
rs547664614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95502276 | AAAATGACAATTAGC[C/T]ATTTTGTTGTTGTTT | 51666 |
rs547711481 | snp | A/G | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:95483376 | TCCTCCATGTATCCC[A/G]TATTCCCTGAAGCTC | 51666 |
rs547722230 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95460137 | TTCCTTTATAAATTA[C/T]CCAGCCTTGGGTATT | 51666 |
rs547729514 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95510066 | AGAAGCTTAAATGCT[A/G]TATCAGAATCCTATT | 51666 |
rs547785303 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95468349 | ATTCATTGACTTGTA[A/G]AGCATGTGGGGGGGC | 51666 |
rs547823385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95513436 | AGGCTGGAGACCTAG[A/G]GAATAGATACAGTCT | 51666 |
rs547837194 | snp | C/G | | | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471179 | GACCTAGGGAGGACC[C/G]TCATTATGAACTGCA | 51666 |
rs547845412 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95461416 | CTATTGGATTTCGGA[C/G]TTGCATGGGACCTGT | 51666 |
rs547884493 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASB4 | GRCh38.p7 | 7:95510810 | GTCTGGATGTGTTAT[C/T]TTTGTTTTATAACTG | 51666 |
rs547935017 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95502793 | ATTTAAAATGTACCA[C/G]AATTGAAAATATATA | 51666 |
rs547983421 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95533591 | AATCTCACTTTGAAT[A/G]CTTTCTTCATTTGGT | 51666 |
rs548060026 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95524158 | AGAGAAATCCCTGCA[C/T]GTGAGCACCAGAGTA | 51666 |
rs548112043 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95465391 | AAGTAAAACTAATTT[C/T]TATGGAATCTAAAAA | 51666 |
rs548121245 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95534071 | CATGAATGGCTGGGC[A/G]CGGTGGCTTACACCT | 51666 |
rs548122929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95526438 | GTGCTGCCGGTTGCA[A/G]CTTTGCAACGCATTT | 51666 |
rs548184380 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95482877 | ATGGGATGGGGGGTG[A/G]TTTAGAAACAACCAG | 51666 |
rs548208909 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASB4 | GRCh38.p7 | 7:95518645 | TAGATAAGGGTAAGA[C/T]AGAGATTAAACTGGG | 51666 |
rs548222118 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95473957 | TTCTTAATCTTTAGG[C/T]TTCACCTTCCTTAAC | 51666 |
rs548256501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95526335 | CTGTGCGCACAATGA[C/T]CTCCTTCAGCACAGC | 51666 |
rs548281597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95519685 | CCTTACGAATAAACC[A/G]TGATAATATTTTCTC | 51666 |
rs548285193 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95475442 | AGGCTGGAGTGCAGT[A/G]GCTCAATCTTGGCTC | 51666 |
rs548288416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95502153 | AGAAAAAGAACAAAA[C/T]GACCAAGAACAGGAA | 51666 |
rs548289636 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538432 | GAGTCCCATGTGACT[C/T]CTGCCTTCCAGGATC | 51666 |
rs548296606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95489597 | AATGTGCTGGTTGGC[A/G]TTTGAGAGACCTCCC | 51666 |
rs548360289 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473305 | AAGGGCTTTACACAT[A/G]TCAACTTAGTTAATC | 51666 |
rs548369147 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95499264 | GAAATCAATGGAATC[A/G/T]CCTGGATAAAGAGTA | 51666 |
rs548371653 | snp | C/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95480809 | GTTGCTTTAAGCCAA[C/T]ACATTTTGAGGTTAT | 51666 |
rs548373065 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95524394 | TGTTTATGATTCCAT[G/T]TATTCAAAGTTCAAA | 51666 |
rs548383047 | in-del | -/T | 0.0146672 | 0.084371 | intron-variant | ASB4 | GRCh38.p7 | 7:95504574 | TTGCCACATCTGCTG[-/T]TATTGTGAGTACCAC | 51666 |
rs548411252 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | ASB4 | GRCh38.p7 | 7:95540522 | TCACCATCTCTGTCC[C/T]CCTGGGGTTTTTCAT | 51666 |
rs548419427 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95488536 | AGCGTGGAGCTGAGC[A/G]GTCTACAGTGGTTAG | 51666 |
rs548427014 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95468247 | AATCTGTCATCAGTC[C/T]ACTCTTTTACACAAC | 51666 |
rs548435340 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95518389 | GGTAGAGATGGCGAA[G/T]CCATAAGACCAAGGC | 51666 |
rs548508563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95517141 | TGGGTTATTTGGCTT[C/T]TTCTATTGAGTTGTA | 51666 |
rs548539864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95534251 | TGGGAGGTGAGGCAG[A/G]AGAATCGCTTGAACC | 51666 |
rs548576139 | snp | A/T | 0.00119737 | 0.0244387 | downstream-variant-500B | LOC107986823 | GRCh38.p7 | 7:95474691 | CATGCCAGGCTAATT[A/T]AAAAAAAAATTTTTT | 51666 |
rs548641788 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515944 | CCCATTGGTACCACT[C/T]TCCTTCATGCCATGT | 51666 |
rs548767589 | snp | A/G | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484142 | AGATCAGCCGGGGGA[A/G]CATGGCAAAACCCTG | 51666 |
rs548771881 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538828 | CCTAGTTGATTACTT[C/T]GGTCTTTTTATGTAG | 51666 |
rs548790546 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95490498 | GGACTGTGTAAATAC[A/G]TGGACACAGGCAGAG | 51666 |
rs548871253 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95533188 | CCAGGGAGAGGCCTG[A/C]AATTTTAGGGTATAA | 51666 |
rs548965616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95497564 | TTTAAAAAGTCAGTT[C/T]ATGGAGGTATAATTT | 51666 |
rs548982339 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95491334 | AGACTCTAGACATGG[G/T]GTAGCGTGTGAGTGG | 51666 |
rs548984735 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95483683 | CTAGGGATTCCCATC[A/G]CCACTTAAATCTGTT | 51666 |
rs549034835 | snp | A/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95476429 | AAAGCTCACAGCCCA[A/T]GTTTAAAATACAAAA | 51666 |
rs549071893 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95527259 | CAAGAAAGCCTCACA[A/G]ACTTGGGCAGCCCTA | 51666 |
rs549072748 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484290 | TGAGCCCAGATCACA[A/C]CACTGTGCTCCAGTC | 51666 |
rs549087769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95499063 | CAGGTTTGTATCAAG[C/T]CTTGAAATCAGATAG | 51666 |
rs549154065 | snp | C/T | | | missense, intron-variant | ASB4 | GRCh38.p7 | 7:95537739 | TACTTGCTTTTAGAG[C/T]CAGAGGGAATTATTT | 51666 |
rs549415354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95499648 | GTAAAAAGAAGTGAG[A/G]CTGCAGAAGTGAACA | 51666 |
rs549486268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95535434 | TGATTTATGTTCTCC[A/G]AAGTTTCATGGGAAA | 51666 |
rs549597856 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95521225 | AAATGTTTCCTTTTT[A/G]AATATGACCTTTATT | 51666 |
rs549628472 | snp | A/G | | | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95474399 | GGATCTTGCTCACTT[A/G]TCAATTTGTTTTTTT | 51666 |
rs549653650 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95540204 | ACTTTTATTTAGAGA[A/G]CTTAAATAAAGCTCT | 51666 |
rs549654052 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95514158 | ACTCCAGTTCCTTGC[C/G]CCTTTTTGAATACAG | 51666 |
rs549654095 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95506051 | GGCACATGGGCCGTG[A/C]CTGGCTAATTTTTAA | 51666 |
rs549670971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95522322 | TGGCAATGATGCTCG[C/T]GGTGTTTGAATTACA | 51666 |
rs549685409 | snp | C/T | 0.000798403 | 0.0199641 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471178 | TGACCTAGGGAGGAC[C/T]CTCATTATGAACTGC | 51666 |
rs549687405 | in-del | -/A | 0.0197687 | 0.0974348 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484330 | GTGAGATCCTGTCTC[-/A]AAAAAAAAATAACAA | 51666 |
rs549689470 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95510518 | TAGAAATAACTAGGC[A/G]TATGTTAAATATCCC | 51666 |
rs549705733 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539750 | GGAAGCTTGAGAGTG[C/G]GGTGAGGGATAAAAG | 51666 |
rs549750668 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95502668 | GTACACTAGAAATTA[C/G]AGACTTTCTCCTAAT | 51666 |
rs549780466 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95470388 | AGGAAATCAGCTCTC[C/T]TTGATCATTTGCTGC | 51666 |
rs549848407 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95459929 | ATTGAATCATGGGGG[C/T]GATTACCCTTATGTT | 51666 |
rs549942242 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95513461 | CAGTCTGTTGCCAGA[A/G]CCCTTCCTTGCTTGT | 51666 |
rs549955632 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95468144 | TTATTAAATTGGGTT[G/T]GGGGGGGCCCCATTC | 51666 |
rs549983854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95511145 | ATGCTAAGAATCAAG[C/T]ACATGCCAGCTTCTT | 51666 |
rs550018584 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95467241 | GTGGTTTTTGTGGCA[A/G]TAGTATAGCCTACTG | 51666 |
rs550028332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95505937 | TTCACTCTGTCACCC[A/G]GGCTAGAATGCAGTG | 51666 |
rs550045939 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95488136 | CACGAGGTCAGGAGA[C/T]AGAGACCATCCTGCC | 51666 |
rs550099902 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95476337 | TGTGTGAGGTAGGTG[C/T]GTATTGCATGCTTGT | 51666 |
rs550116502 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95483572 | TGGGGGATCAGATCA[A/G]ATGATTAGATATAAA | 51666 |
rs550124085 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95503064 | ATTTTTCTGAAAATT[A/G]TATGTGACTATGCAT | 51666 |
rs550127214 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95522535 | TGTTAGGCAGGGCAT[A/T]GTATTTATTTTTAAA | 51666 |
rs550166684 | snp | A/C | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95460958 | ATAGGGGCCAATGTG[A/C]AGCTCAGGCCATTGC | 51666 |
rs550242398 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513192 | AGGAAATGGACTCTT[C/T]TATACATTCTGGTTG | 51666 |
rs550266154 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95523091 | CATACTGTAAGAATG[A/T]CAATTCTTCCTAAAT | 51666 |
rs550362601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95527115 | TATTTCTACTATACC[A/G]GCTTCTGCCCCTTTT | 51666 |
rs550409428 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95491455 | GTGAAGTCTAAACAC[A/G]TAGTAAAAGGGCAGC | 51666 |
rs550498548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95520877 | TTGCTTTGATATTTG[A/G]TGGGGTAAGTACCCC | 51666 |
rs550571770 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95485036 | TATATATGTATATAT[A/G]TATATATATGTGTAT | 51666 |
rs550582081 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95528909 | TAAGTAGCTTACCTG[A/G]GCTCCCACAGTGCCA | 51666 |
rs550588855 | snp | C/T | 0.00159617 | 0.0282053 | nc-transcript-variant, intron-variant | LOC107986823 | GRCh38.p7 | 7:95471324 | GTCCTCTTTCCTGCA[C/T]GCTTCCTCATTTGCA | 51666 |
rs550655419 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95536935 | TCATGAAGTGACTAT[A/T]AGGCAGGAAAGAGTT | 51666 |
rs550703331 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95499967 | CAAGCTCTGCCTCCC[A/G/T]GGTTCACGCCATTCT | 51666 |
rs550709962 | snp | A/C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515771 | CTGGTATTCCCCCTG[A/C/G]ACTAAAGGACTCCTT | 51666 |
rs550710428 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513771 | GCTGCCCAGTTTGTG[C/G]TAACTTGTGACAGCA | 51666 |
rs550721773 | in-del | -/T | 0.00199481 | 0.0315187 | | | GRCh38.p7 | 7:95466058 | ATGTCCTAGGCCCTA[-/T]TATCAAGTATTACCA | 51666 |
rs550727594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471750 | GTTGACTGCAGCTGG[A/G]GCAAAGGTAGCAGGT | 51666 |
rs550766934 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95480264 | CTGTTTTTTTGTCTG[G/T]TCCCTTGTAGCCCCT | 51666 |
rs550790054 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95516101 | GAAGAAGTCCTTATC[A/C]CTTTATCCAAACTTG | 51666 |
rs550928320 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95507379 | GAATGCTCTGCTCCT[A/C]TTCTTTGCCGAGCAA | 51666 |
rs550954108 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95499093 | GAGTGAGTCCTCCTA[C/G]ATCAGTTTTAAGTAT | 51666 |
rs551032241 | snp | A/G | 0 | 0 | intron-variant | ASB4 | GRCh38.p7 | 7:95531520 | TAATTAAATGAGATA[A/G]CATTTGAGAAGTGGT | 51666 |
rs551038542 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95536659 | GAGAATGCCTTTAAA[A/G]CGTACTCAAATGCAA | 51666 |
rs551092800 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515183 | TCTTTCTTTCTTTCT[C/T]TCTTTCTTTCTTTCT | 51666 |
rs551194970 | snp | A/T | | | | | GRCh38.p7 | 7:95460766 | TTAATCACCAAGACA[A/T]TGGGGAAAATGTCTC | 51666 |
rs551199480 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95497658 | ATGCCAATCATCTTA[A/C]AAAGTTTCCTGATGC | 51666 |
rs551215940 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95463119 | GCATGATCATAGCTC[A/G]CTGGAACCTTGAACT | 51666 |
rs551238370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95534989 | ACCAGCTCTGACCTT[C/T]AGCCCTGCCCTGACT | 51666 |
rs551278704 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95507878 | TAAACAGCTGCTATT[G/T]GATTTAGTGACATGG | 51666 |
rs551475073 | snp | C/T | | | | | GRCh38.p7 | 7:95478926 | TAGCAGTTCTTCCAG[C/T]GCCCCCAACTGCTTG | 51666 |
rs551549174 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485787 | CCAGTTTAAAGGACC[G/T]GAAAATGTAGTGACA | 51666 |
rs551621502 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95536203 | CATTCCAGGGAGCTT[A/C]ATAGGTCTGTGGGTT | 51666 |
rs551635823 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95462498 | CCTCTGTGACAGTAA[A/G]TTTTCAAATGGCTTA | 51666 |
rs551724173 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95514195 | CACCCTCTCTTAACG[G/T]CATTTCTTTCTCTAC | 51666 |
rs551772390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473170 | ACAAAAAGGGAATTT[C/T]TCACCTCTATCCGTC | 51666 |
rs551902451 | snp | A/C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95524251 | ATCTACAGTTGAATG[A/C/G]ATAAATTGTGGATTA | 51666 |
rs551903366 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95464049 | TATCTGATGATTGTG[A/G]GTTTTAGACAGATAG | 51666 |
rs551957955 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471654 | AATTGAGGTCCTAGC[A/T]TAATGCCCTCTTTTC | 51666 |
rs551987815 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95522934 | TGAAGGAACTTCTCC[C/T]ATTAAAAGTCACTTT | 51666 |
rs552019236 | snp | A/G | 0.000399281 | 0.0141238 | nc-transcript-variant, intron-variant | LOC107986823 | GRCh38.p7 | 7:95471278 | GTCTGAGTCAGGTTT[A/G]CTTCCCCAGAGCTCC | 51666 |
rs552028206 | in-del | -/AGATAAAAGGAA | 0.00438332 | 0.0466095 | intron-variant | ASB4 | GRCh38.p7 | 7:95518853 | GTGACTTCAGGACAG[-/AGATAAAAGGAA]GACTTGAGCCAGACA | 51666 |
rs552083868 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95480720 | TTTGAGGCCACAGAC[A/G]TCATAGAGCAGAGAC | 51666 |
rs552104946 | snp | A/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95464930 | ATTGACAACAATAAG[A/T]TATTTTTCTCAATAT | 51666 |
rs552117434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95506896 | CTATTATTTGGATAT[C/T]GAACCTCCCTGGACT | 51666 |
rs552175535 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95516306 | TGAGTTATTCAGTCT[C/T]ATCTATGGTTACTTT | 51666 |
rs552176185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95517066 | TCCCTGTGTTAATGA[C/T]CATTTGCATGGTTTG | 51666 |
rs552252758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95532936 | GGAGGCTGTGGTTTC[C/T]CCCTTTGGGGTCCAC | 51666 |
rs552255715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95525673 | AAATTCTCCAGCATC[C/T]GAAGTGACCCTGCAC | 51666 |
rs552274309 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95508823 | ACATTTAATGGACAA[A/G]GAGAACACAGAGAGG | 51666 |
rs552279778 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95482144 | TTTTATCCTTTGCTG[C/T]TCAGGTAAAATAATC | 51666 |
rs552281420 | snp | A/G | | | | | GRCh38.p7 | 7:95462959 | GAGAATCCTAAGGGA[A/G]ACCCAGAGAAAAGAG | 51666 |
rs552289997 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95489272 | TTTGTGAGGAAGACA[A/G]AATAAAGCTATTGGA | 51666 |
rs552344631 | snp | A/G | | | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95473868 | ATGAGAGCAGGGAAG[A/G]GGATTTACTCACTGG | 51666 |
rs552392415 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95502068 | AAAGGGCTTACTATA[A/C/T]GCAGAAGTTTTTCAA | 51666 |
rs552462995 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95517936 | AAGAGTCCATGGGAA[G/T]GGAGATGTTGGGTAA | 51666 |
rs552493470 | in-del | -/TGTATATATGTGTG | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484995 | ATATATGTGTATATA[-/TGTATATATGTGTG]TGTATATATGTGTAT | 51666 |
rs552572111 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538747 | AAAAATATTGCACAC[C/T]CAATGGCTCCAGTGC | 51666 |
rs552584449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95490774 | CTACCCAGCTATTGG[A/G]GCATATCTCTTTGGT | 51666 |
rs552588887 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95500970 | TTTTCTATGTGTAGC[C/T]ATCACCACTCTTCAC | 51666 |
rs552595984 | snp | G/T | 0.00159617 | 0.0282053 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95474057 | TGTAAAGCTAGATTT[G/T]TATGTGTGGTATTTG | 51666 |
rs552630155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95518587 | TAAGGAAAAAAATTA[A/G]ACTATATTGGCACTC | 51666 |
rs552665536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95507410 | ACTTCTACTCCTGTG[C/T]GAAGTCTTAGTTCAG | 51666 |
rs552674798 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95521178 | TCATAGTAGATCTTT[A/G]TATATTCTGATTATG | 51666 |
rs552675431 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ASB4 | GRCh38.p7 | 7:95505967 | GGCATGACCATGGTT[C/T]ACTGCAGGTTTGACT | 51666 |
rs552676361 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95489730 | AAAGAATGACTTTCT[A/G]ACTGCCAAATGCAAT | 51666 |
rs552706411 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASB4 | GRCh38.p7 | 7:95527430 | TCAAGTGTTGTGACA[C/T]AACATTTGTTTTTAA | 51666 |
rs552737937 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95492126 | GAGTTGTAACCACAA[C/G]TCCATTCTGGGAGTT | 51666 |
rs552749551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95492880 | AAGTTAATGTGATTC[A/G]TTCATCATCAAAAGC | 51666 |
rs552810869 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95499337 | CTAACATTTCAATGT[C/T]AGAAGGATGAGGAGA | 51666 |
rs552850897 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASB4 | GRCh38.p7 | 7:95513930 | TCTGCCATCATCCAC[A/G]AAGGATTTCGATGCT | 51666 |
rs552864170 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95521899 | TCTGTGGAGGAAAAA[A/G]TTATGGGAGAAAGAA | 51666 |
rs552871366 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538343 | AAATGAGAAAGAAAC[A/G]TCAGTCCAGTTAATA | 51666 |
rs552894833 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95477763 | TTTGCTATAATTCTG[C/T]GATTCTACAAGCAAA | 51666 |
rs552987554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95499974 | TGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT | 51666 |
rs553028152 | snp | A/C | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538094 | CAGGTTTTCTTCCAA[A/C]CAATATAATTCTGTG | 51666 |
rs553096882 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95507092 | ATTTAAGATCCGAGT[C/T]ACTAAAAGCTGATTT | 51666 |
rs553106324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95529071 | GACTAAGACATGGGA[C/T]GTATCCTCAAGAAGC | 51666 |
rs553111197 | snp | C/T | 1.9747e-05 | 0.00314215 | intron-variant | ASB4 | GRCh38.p7 | 7:95536394 | AGAATGAATGAACCA[C/T]ATATGTGCATCAAAC | 51666 |
rs553186938 | snp | A/G | | | | | GRCh38.p7 | 7:95463138 | GAACCTTGAACTCCT[A/G]GGCTCAAGCAATCCT | 51666 |
rs553259454 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant, intron-variant | LOC107986823 | GRCh38.p7 | 7:95471357 | ACAATGTGAATTCTG[C/T]TCTTGCCCTTATAAT | 51666 |
rs553279920 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95485426 | AAATTTTTCAAGTCT[A/G]GGTCACTTGAAAACC | 51666 |
rs553328720 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95462098 | CTAATATAGTGGCCT[G/T]CTCTAGCACCCAGGC | 51666 |
rs553333601 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95481300 | TGCTGGTGTTACTTA[C/T]AAACAAAGGCATCTT | 51666 |
rs553341210 | snp | G/T | | | | | GRCh38.p7 | 7:95479864 | AAATATCTGAAAAGA[G/T]GTGCAGGCATCTGAA | 51666 |
rs553377795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95523497 | ATAATCAAATGAATT[C/T]GGATTTTAAAAAATA | 51666 |
rs553415278 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95481771 | TACACCAGGGTCTTA[C/T]GGGCCACTTGCCACA | 51666 |
rs553443457 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95516455 | TCCTTTCTTTAAGGT[G/T]GAGTAAGTTAAAAAT | 51666 |
rs553493632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95508358 | TATGTAAAGTAAGAA[A/G]TGAAGAGAGTTGAGA | 51666 |
rs553526730 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95495227 | GCAAATAAAATCTTG[A/G]AGTGATAATTTTTTT | 51666 |
rs553570348 | snp | A/G | | | intron-variant, utr-variant-3-prime | ASB4 | GRCh38.p7 | 7:95528772 | AATTATATTTATTAT[A/G]TATAATAAATAAGCA | 51666 |
rs553574186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95493571 | CTTATTTTGATTTTA[C/T]TTATTTTTGTTAAAA | 51666 |
rs553585471 | snp | C/T | 0.000197834 | 0.00994373 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95486121 | CACTGTTTTTGAAGT[C/T]GAAGATGAGAATATG | 51666 |
rs553644001 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95491415 | ATGGGCTTGGTTCCC[A/C/G]GGTTCTCCCTCACCT | 51666 |
rs553670467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95486831 | AGGAAAACAAAAATT[A/G]GACCAATTTTTTTTT | 51666 |
rs553725618 | snp | C/T | | | | | GRCh38.p7 | 7:95461304 | AGAGGTGAAGCTGCC[C/T]AAGGCTGTGGGGGCC | 51666 |
rs553754506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95532024 | TTTTGTTGCTACTCA[A/G]CAGACTGTGTAGGAG | 51666 |
rs553756170 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538537 | CAGACTCACTTTTAA[C/T]GCTTATCTTTCAAAG | 51666 |
rs553817885 | snp | A/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95537964 | TTTTCAAAGACAAGG[A/T]TGTATTCAGAATGTA | 51666 |
rs553893461 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95459641 | TGGTTCTGCCACTGC[A/G]GTGCCATTGTGGTGG | 51666 |
rs553912613 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95512387 | TGGATTATGTAAGGC[A/T]CTTTTCCCCCATCCC | 51666 |
rs553947276 | snp | A/T | 0.000399281 | 0.0141238 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95474296 | CCTTTTGGGGAGGTC[A/T]AATATAAAAATAGGA | 51666 |
rs554032744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95511430 | CCTGGGTGGTAAGAG[C/T]AGGAAGTACGTGCAC | 51666 |
rs554036333 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95509239 | CTAAAGAAGTAGGGG[A/T]GTTCTTTTTATTTAT | 51666 |
rs554036558 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95501011 | TCATTTATGTTTAGA[A/T]TTAGTTTTTATCTTT | 51666 |
rs554046256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95525855 | GCCTTCTACAAGTTA[A/G]GAATACAGTCTCAGA | 51666 |
rs554052679 | snp | A/T | | | | | GRCh38.p7 | 7:95479279 | AGTATTTCTCAGGAA[A/T]AATTGTGATGTTCTA | 51666 |
rs554079418 | snp | C/T | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469280 | CTGGAATGATAGAAT[C/T]TTTGAGGTCAAAAGG | 51666 |
rs554190589 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASB4 | GRCh38.p7 | 7:95489760 | TAAGTCATTGAAAGT[C/T]AAGGGATGTCAGTGA | 51666 |
rs554202263 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95487906 | TTACTTTTAGGGTTT[A/T]TGCAGGAAATTTGTG | 51666 |
rs554266566 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539200 | CTTTTATGTGTGTGG[G/T]TCTCCATCATATTTA | 51666 |
rs554266825 | in-del | -/TC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515196 | CTTTCTTTCTTTCTT[-/TC]TTTCTTTCTTTCTTT | 51666 |
rs554339313 | snp | A/C | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95464398 | GAGATTCTGTTAGAC[A/C]TAGATTGATAAATAA | 51666 |
rs554353688 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95463485 | GGTGATTGGTTCATG[A/G]GAGCAGTTTCTAATG | 51666 |
rs554475731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472623 | TCTCACTAATAGGGG[C/T]TTTAATGATGCTCTG | 51666 |
rs554498334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95507710 | GCACTAGGGAAAAGA[A/G]TGCAGTTGAACCAGA | 51666 |
rs554605254 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ASB4 | GRCh38.p7 | 7:95498864 | GTCTTTTTTTATATG[G/T]ATGCCCAGTTGTTTC | 51666 |
rs554746935 | snp | A/C | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95485308 | ATAAAGTTCATTCAC[A/C]TGTTGCATTTAAATG | 51666 |
rs554777972 | snp | C/T | | | | | GRCh38.p7 | 7:95464869 | ATCTTGACTTACAAA[C/T]ATCTCAATTTCTACA | 51666 |
rs554837920 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95517962 | GGTAAATAATAGAGA[C/T]AAATTACTTGTGGAG | 51666 |
rs554841834 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95507945 | GATGCAGAAGTCAGA[G/T]TGGGGGGGATTGAGA | 51666 |
rs554842859 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95500810 | ACTTACTTTGGCACA[A/C]AAGGTTTTCCTCTGA | 51666 |
rs554893601 | snp | C/T | | | | | GRCh38.p7 | 7:95464173 | TGGTTTATTTACTTT[C/T]TTCACCCTTGACTAT | 51666 |
rs554916237 | snp | A/G | 0.00159617 | 0.0282053 | | | GRCh38.p7 | 7:95478480 | AATTCAGGTGGGCCA[A/G]TGCTTGGTTACTGCT | 51666 |
rs554918380 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469047 | ATGGGGCAATACAAA[G/T]TTCATTCCATTTGTT | 51666 |
rs554971275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95525327 | CTTGGAAACTAATAC[A/G]TTGTATTTTCACATT | 51666 |
rs554996360 | snp | G/T | 0.00835141 | 0.0640778 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95485155 | TGACAATTTATCCCT[G/T]AATGTATCACTTAAG | 51666 |
rs555003001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95495359 | TCATTCAAGACAAAC[C/T]CTCAATGATTGAAAG | 51666 |
rs555012085 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95466735 | ATGGACTAACAATTC[C/T]ACATGGCTGGGGAGG | 51666 |
rs555053805 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95475680 | TGAGCCACCGTGCCC[A/G]GCCTTGAATTTATTT | 51666 |
rs555106186 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539079 | TCACTTTTTTTTTTG[C/T]TCTTGCTATAATCAC | 51666 |
rs555115785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95524632 | CCAATACCTCAGCAC[A/G]TGAATTTATTTGGAA | 51666 |
rs555129796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473603 | GAGCCTATAGAATAC[A/G]GATGCCATTGTGAAT | 51666 |
rs555134663 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95459620 | AGAATACGATGCTCT[A/G]CCCACTGGTTCTGCC | 51666 |
rs555143685 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95468670 | CCGTCATTTAATTTT[G/T]TACAAAATTCAATTG | 51666 |
rs555193072 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95481220 | GACCTCTGCTGAAAC[C/T]CAAACACTACAACTG | 51666 |
rs555355936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95533810 | GTTAAAGTATATGAA[A/G]ATTTAACACAGTCCC | 51666 |
rs555389469 | snp | A/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95475062 | AGCTGTTTTTTATGT[A/T]TAGTGCCTAGACCAG | 51666 |
rs555405596 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484608 | CATTTACATGCTTAA[C/G]TAAATTCTAAGAATC | 51666 |
rs555431024 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95533621 | TATCTTTCACTCTGA[C/T]ATGTCTGGTGTTTTT | 51666 |
rs555449411 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95483068 | CCGACGGGCTGCAGC[A/G]TTTGAGAACATCAAA | 51666 |
rs555492446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95512167 | CCAAGGGCTGGCCAG[A/G]AGGCTCGAACATGGC | 51666 |
rs555510672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95520026 | TGTTTGGAGATGAAA[C/T]GGGTAGGTTCAGTTT | 51666 |
rs555554698 | snp | C/T | | | | | GRCh38.p7 | 7:95483158 | CGACCCATTCTGCCA[C/T]GGAGATATCAGGGAG | 51666 |
rs555618161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95525944 | TTGAGCATGCTTGTA[A/G]GAGTTTTGGCTTTCT | 51666 |
rs555682029 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95533376 | TTGGGCTTCTAACAC[A/T]CTTCGTGCTGTGACA | 51666 |
rs555712451 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95491601 | TAAAAAATGAATCTG[A/C]CTCATCAGTTAATTG | 51666 |
rs555739723 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95497863 | GCATGGACCAATAAA[C/T]TAGACCTTTTTATTG | 51666 |
rs555802711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95505173 | AGGAAGCAAAATGGC[C/T]GTTATTTAAAACAGG | 51666 |
rs555811559 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | LOC107986823 | GRCh38.p7 | 7:95474997 | AATATGATCCTTAGG[A/G]TGAGGTGGCTTTCTA | 51666 |
rs555822127 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | ASB4 | GRCh38.p7 | 7:95540509 | TCTCCTCTGCCTCTC[A/G]CCATCTCTGTCCTCC | 51666 |
rs555841430 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95533345 | AGGTCCTACACTAAA[A/T]AGGGAAAATTACTTA | 51666 |
rs555869810 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95482528 | CTTACAAAGACAGCC[A/G]TTGTGAGACTCAAGG | 51666 |
rs555904389 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538953 | ATGGTAAAAGTTTGA[A/G]AAACTTGGGAAGATT | 51666 |
rs555933319 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95489522 | ATAAAATCTGCAGAT[G/T]AAATCATGTTTTATT | 51666 |
rs556136947 | snp | A/C/T | 0.0023933 | 0.0345097 | | | GRCh38.p7 | 7:95479416 | TGGTAATTATTCTTA[A/C/T]GAAATAGTATGCTTA | 51666 |
rs556140646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95532561 | TGAACAATGCTGTAT[A/G]TGAAGGTAGGCAGTT | 51666 |
rs556169157 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95481948 | GCCTGACTAGACAGT[A/G]TGAAACATGACCACT | 51666 |
rs556258601 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95490477 | GCTTCAGTCTGTAAT[C/G]CTTCAGGACTGTGTA | 51666 |
rs556273408 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95526468 | TTCATACATACTTTC[G/T]CTAATAAATCTGCCT | 51666 |
rs556344684 | snp | C/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95467767 | TCCTGAACTTTCCAG[C/T]GGGGCTTGCATAAAT | 51666 |
rs556346629 | snp | C/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95475620 | AACTCCTGACCTCAG[C/G]TGATCCACCCACCTC | 51666 |
rs556432391 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95502339 | TATATGACAAACACA[C/T]AGGGAAGTGCTCTTA | 51666 |
rs556456967 | snp | C/T | 3.29821e-05 | 0.00406078 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95495906 | GAAAACCCCTCTTCA[C/T]GTGGCTTGTGAAATG | 51666 |
rs556480472 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95540008 | TGATGCACTGACTTG[C/G]GGCAAGTAAAACTGA | 51666 |
rs556522383 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95495242 | GAGTGATAATTTTTT[A/T]AAAAAGATTAAATAT | 51666 |
rs556575878 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95504154 | CTACCTATTCCATTC[A/G]TAAGAGGAAAATGAA | 51666 |
rs556610595 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95460202 | AAATTGGTACCACAG[A/G]GAGTGGGATGCTGCT | 51666 |
rs556641676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95514255 | AATTTCTGTCTCACC[A/G]ACACTATAACTTTGC | 51666 |
rs556653353 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95513904 | TGTCAATTCTGGTCC[A/T]TTTCTCTAATTCTGC | 51666 |
rs556692725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95527435 | TGTTGTGACATAACA[C/T]TTGTTTTTAATGATA | 51666 |
rs556730020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95524804 | CCAGAGACCCTCTAA[C/T]CAGCCTGTGCACTGG | 51666 |
rs556757340 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95534481 | TCTTTCTTCCTCCTA[A/T]CTGATTAGTATTAAG | 51666 |
rs556760988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95519978 | TTCAAAACAGAGTAG[A/G]ATAAAAAAAATCTTC | 51666 |
rs556868609 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515193 | TTTCTTTCTTTCTTT[C/T]TTTCTTTCTTTCTTT | 51666 |
rs556991596 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95462009 | GTGCCATGTGGAACT[A/G]TTAGTCAATTGACCC | 51666 |
rs557008242 | snp | G/T | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538170 | CAGGCTTTGCAATTG[G/T]CCTCTTAAACTTGGT | 51666 |
rs557011428 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95480194 | CCTAGACCTTACCCA[A/G]TTTACTTTTCTTGGT | 51666 |
rs557014586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95506927 | GTTTCTCTAATTATC[C/T]TGTATTGTCTCGTCT | 51666 |
rs557070820 | snp | A/G | | | | | GRCh38.p7 | 7:95482993 | CTTAGGTTCATGTCT[A/G]TTCTGGCCCTAAGAA | 51666 |
rs557072171 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95535021 | CATCCAGGTTGGCCT[C/T]TTTACTGTCAACACA | 51666 |
rs557126139 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95462587 | TCTGTCATCTAGAAC[A/G]AGAAGATAATGAATG | 51666 |
rs557190582 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95477702 | CAGTACTTTTTTTCT[C/T]AAATGAGAAGATTTG | 51666 |
rs557310895 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95479474 | AAAAGTATAGTTTTA[A/G]TTGTACTAGCTTGCT | 51666 |
rs557332061 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95485408 | TCCCAGCTTTTCATA[C/T]TAAAATTTTTCAAGT | 51666 |
rs557354434 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95529258 | TTTTACCTGAAAATA[A/C]ATCAAATAATACTAT | 51666 |
rs557392553 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95490984 | GGGCAATGGAGTTTG[A/G]GAGTTAGAGTTGATT | 51666 |
rs557414998 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95535637 | TAAATGTTAAAGCTA[A/C]ATCTTTCTATCTCCT | 51666 |
rs557460091 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469515 | TGTGAACAGGAATGA[G/T]AAAATTTTCCATTTT | 51666 |
rs557471270 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95523947 | TGCAATGAGATATCA[C/T]TCTGCAACCAAGAAA | 51666 |
rs557485409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95515614 | AGAGACGGGGTTTCC[C/T]CATGTTGACCAGGAT | 51666 |
rs557497949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95523448 | AAAAGAAATACCATT[A/G]GTTAATAATTACAGA | 51666 |
rs557500715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95488455 | AATGACAAATAGAAT[C/T]CTAGCTGCTAGTAGA | 51666 |
rs557545240 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95507615 | CAGAGACTGTTTTGC[G/T]TGGCAGAGCCCAGTG | 51666 |
rs557606393 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95527393 | TTTTGTGGAATATTC[G/T]AAACAGTTGATTTTT | 51666 |
rs557644719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95493535 | AAATTATTTTTTCCC[C/T]TCTGGACAGAGAGAC | 51666 |
rs557682312 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539892 | CTATTGAAATCTTAA[A/G]ATAGTAATAATTAAC | 51666 |
rs557682336 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95534931 | AGTCAATCCCAAGCT[C/T]TTCAGGCTGACTTCC | 51666 |
rs557706826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95490360 | ATGTTCAAACTTTTT[C/T]CTTTTACATTTTACA | 51666 |
rs557707694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95492691 | ATTGCAGAAGCAGGC[A/G]CAAATTTCCAATCAG | 51666 |
rs557710379 | snp | A/C | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95477825 | TTCTCTTTAGGTATA[A/C]TATTTTTCTATGGTT | 51666 |
rs557796269 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95478678 | TGGGATCCAAGAAGT[A/G]GGCAGTAGCGGCTAA | 51666 |
rs557821495 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95513747 | AATAATCAATTTGTG[C/T]TGTTTTCAGCTGCCC | 51666 |
rs557885657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95505294 | AATATACAAAAATCA[A/G]TTGCATTTCTGTATA | 51666 |
rs557886798 | in-del | -/TGAT | 0.00279162 | 0.0372561 | intron-variant | ASB4 | GRCh38.p7 | 7:95533301 | TGATATTCTGATCTC[-/TGAT]TGTCATCTTCATTTC | 51666 |
rs557963557 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95483116 | AGAATCACACACTCT[A/G]GTAGCCAGATAGGAC | 51666 |
rs558007952 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95520188 | AGTGTCCCCCCAACA[C/G]GGGCACATGTGCCTC | 51666 |
rs558084067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95535541 | AATGGAAAGAAAGAT[A/G]ATTAAACTGGGAGTC | 51666 |
rs558135706 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95525324 | GCTCTTGGAAACTAA[A/T]ACATTGTATTTTCAC | 51666 |
rs558135746 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | ASB4 | GRCh38.p7 | 7:95528486 | TCCTAGTCTAGGTTT[G/T]CTTGAAATTGGGTGT | 51666 |
rs558155615 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95527416 | TGATTTTTAAAGAGT[C/G]AAGTGTTGTGACATA | 51666 |
rs558196783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95535140 | TCTGTCTCTGTTTTA[C/T]CTGTGATCCCAAGAC | 51666 |
rs558252727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95493685 | CATTTCTGTCCTGAT[C/T]CCCCAACCCCCCAGT | 51666 |
rs558254765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95500717 | ATTCTCTGGATTTCA[C/T]CTCATCTCAACTTCT | 51666 |
rs558269593 | snp | A/G | | | | | GRCh38.p7 | 7:95464568 | AGGCAGCTTCTCTGC[A/G]GTTAATGAAATTATC | 51666 |
rs558306278 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95508004 | AACAAGCCTTTTAAG[A/G]AGTATTTGTGAAGAG | 51666 |
rs558324227 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471861 | TTCTTAGGCAGGTAC[G/T]ATTATTATCTGCTTT | 51666 |
rs558336371 | snp | C/T | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:95479389 | CGTTGTTTCATGTGA[C/T]TTTTACAACCCTGGT | 51666 |
rs558336472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471484 | AATGAAGACATGTCA[A/G]AATAGGTTTCTGTTG | 51666 |
rs558386952 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95519584 | AACCAACATGGATCA[A/G]ACATCTCAGATAAAA | 51666 |
rs558424914 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95498027 | GGACTTTTTATTTCT[C/T]TTATATAAATACCTA | 51666 |
rs558439604 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95507121 | TTGGAATCTAATTAT[A/C]TACGTAGAGGTTTTT | 51666 |
rs558446439 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | ASB4 | GRCh38.p7 | 7:95536121 | TGATTTTATTAATCT[A/C]TCTATTTGCCATGGT | 51666 |
rs558446596 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95499263 | GGAAATCAATGGAAT[C/T]GCCTGGATAAAGAGT | 51666 |
rs558476009 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95501270 | TCAAATGTTTCTTAG[C/T]AGAATGTAGCATGGG | 51666 |
rs558551574 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95502558 | TGTTATCTCTGAACT[A/G]GGTTATACCTAAAGT | 51666 |
rs558757475 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant, intron-variant | LOC107986823 | GRCh38.p7 | 7:95471354 | AAAACAATGTGAATT[C/T]TGTTCTTGCCCTTAT | 51666 |
rs558780702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95510195 | ATATGAAAAACTGTC[A/G]ATGTTTCTTCCGAAA | 51666 |
rs558784721 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95517856 | AGCAATAGAAAGAAA[A/T]TGGAGGTTAGCTAAA | 51666 |
rs558813594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95507604 | TTTCAGGAGACCAGA[A/G]ACTGTTTTGCTTGGC | 51666 |
rs558832691 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95535379 | ATGCCTCACCTAACA[C/T]CAAGTGAAAGGGGCT | 51666 |
rs558848436 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538317 | ACAAGGAGATCTTGG[A/G]GTCAAATTAGAAATG | 51666 |
rs558864325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95524035 | GAAACCCTCACCCAT[A/G]GCTTATCGGAGTGTA | 51666 |
rs558877903 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASB4 | GRCh38.p7 | 7:95517342 | CCAGGTCTAGTTTTA[A/G]TAGTTCTTTATGTAT | 51666 |
rs558984529 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95465830 | ACTCGGGAGATTGGA[A/G]TAAGAGGATTGCTTG | 51666 |
rs559010393 | snp | C/T | | | | | GRCh38.p7 | 7:95483038 | AGATGACTTGTTCTT[C/T]ATCGTCCTTGTCAGC | 51666 |
rs559050233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95535295 | GGTTGAGGTTGATAC[A/G]GTCTGGGAAATTAGG | 51666 |
rs559086512 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95513184 | AAAAGGTAAGGAAAT[G/T]GACTCTTCTATACAT | 51666 |
rs559111734 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95491370 | ATTAGAGGGAGGCAG[A/C]CGCTGCTTCACCTCC | 51666 |
rs559124964 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95537187 | TTCTGCTACTTATTG[G/T]CTGTGTTACTTTTAA | 51666 |
rs559153012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95486852 | ATTTTTTTTTACCAA[A/G]GAATTTTCTGGAACC | 51666 |
rs559211710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95506414 | TGGACCACAAGTCTT[C/T]CTAAATCTTGGTGTG | 51666 |
rs559373747 | snp | A/G | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95483458 | ACTGATCATTTACCT[A/G]AAGAGACTGCTAAAT | 51666 |
rs559412079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95492205 | TGTTTATGATTACAG[A/G]AGATGCAGAAGAAAC | 51666 |
rs559478494 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95463533 | TAGTGCTGCTCTTGC[G/T]GTAGAGTTCTTACAA | 51666 |
rs559499827 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469836 | GTAAGTTCTATTTTC[C/T]GTTATATCAGTCTTA | 51666 |
rs559504216 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95529953 | TTACTTAACACCTCC[A/G]AAGTGTCAGGTACTG | 51666 |
rs559590484 | snp | A/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95460805 | GTCAGAGACCTTCAA[A/T]GTAGCCCCTCTCATC | 51666 |
rs559637515 | snp | A/C | | | | | GRCh38.p7 | 7:95476403 | TTTTATATTTAAAAA[A/C]AAATTTATAGAAAGC | 51666 |
rs559700746 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95462868 | GATTTGGGAACTATT[A/G]TAATGGTTGACTCCA | 51666 |
rs559711498 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | ASB4 | GRCh38.p7 | 7:95528659 | AAACAGAATGACTGA[C/T]CTAAAGATGACTCAG | 51666 |
rs559757801 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95515735 | TGCTCTTTCTGTAAG[A/G/T]CACTGGTTGTAGAAT | 51666 |
rs559783348 | snp | C/T | 0.000798403 | 0.0199641 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95473765 | GCTGGAGAGACAGAA[C/T]CAACAGATGGGGAAC | 51666 |
rs559877873 | snp | A/G | | | intron-variant, utr-variant-3-prime | ASB4 | GRCh38.p7 | 7:95528589 | TCCTGAGGGACTGAG[A/G]TAAGTCTGCCAGAAA | 51666 |
rs559887479 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95507804 | GAAGAGAGTATGTCA[C/G]GAAGGAGGGAGAAGT | 51666 |
rs559961308 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471610 | AAACTCATTTGGAAA[A/T]AAACAATAATTGTCT | 51666 |
rs559962885 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95478978 | TGTGGACAAGGGCAG[C/G]CCATAACATGGCTGC | 51666 |
rs559966260 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95487285 | ATATTTTGATGGGAA[G/T]ACAAAGAAGGGATCT | 51666 |
rs560024224 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95532205 | GAAGATAAAGTGATT[C/T]GTTCTTGTGTGGATG | 51666 |
rs560043657 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95522853 | AAAATTTAATTTTTT[A/T]TCTCTCTCATTTACT | 51666 |
rs560075665 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473030 | AGTGGCAAGTTTCCA[A/T]GGAGTCGGTAGCTCC | 51666 |
rs560076170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95515103 | AGGTACTCCTTCCTC[A/G]TATGAATTCCCAGCA | 51666 |
rs560158345 | snp | A/C | | | | | GRCh38.p7 | 7:95465675 | TGGCTAATTTTTAAA[A/C]ATTTTTTTAGAGATG | 51666 |
rs560200158 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95494145 | CAGGAGTGGCATGTC[G/T]CTAGTGTTTTTCACT | 51666 |
rs560205669 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95531326 | CTAGAAGACAAAAAC[A/G]TCTACCTCTGTAATA | 51666 |
rs560232549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95517015 | TGTTTAGTTATCCTC[G/T]CAAGCTTTCCATGTC | 51666 |
rs560239455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95532825 | ATAACTTTTTTGTCT[A/G]ATTGTTCCTCCATGA | 51666 |
rs560246015 | snp | G/T | 0.00199481 | 0.0315187 | nc-transcript-variant, intron-variant | LOC107986823 | GRCh38.p7 | 7:95471327 | CTCTTTCCTGCACGC[G/T]TCCTCATTTGCAAAA | 51666 |
rs560287544 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASB4 | GRCh38.p7 | 7:95509627 | AGGATAAATGCTTAA[C/T]GGAAAATCTAGCTTA | 51666 |
rs560307337 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95491959 | CATTACCACCAAAGT[C/T]TTGCAACACAGCTTC | 51666 |
rs560322815 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95493846 | TTCCATTTCAGTCTA[A/T]ATAGAACTGCCCCTT | 51666 |
rs560378182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95536686 | GCAATGAGACAAAGG[A/G]TTATAAAATGCAGGT | 51666 |
rs560402470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95502433 | ATCAAAAGCTTAAAA[C/G]TTTCTTGTAACTTAG | 51666 |
rs560424863 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASB4 | GRCh38.p7 | 7:95502044 | GGAAAATATTTGAGA[C/G]TATATGACAAAGGGC | 51666 |
rs560472398 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95537455 | ATTTTTGCCTCACCA[A/G]TAGAGACCCTAGGAA | 51666 |
rs560524918 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95466025 | ATGATAATAAGCTGC[C/G]ATTTACTGGACTCTT | 51666 |
rs560568720 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95488437 | TGGAAAGTTAGGAAT[G/T]GAAATGACAAATAGA | 51666 |
rs560803135 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485599 | TGGATCTCCAGCCAG[C/G]CACCAGATGTTTTTA | 51666 |
rs560803372 | snp | A/G | 6.59348e-05 | 0.00574135 | missense | ASB4 | GRCh38.p7 | 7:95486054 | AGGCGCTAAAGTCCA[A/G]TGACTTCGGAAAATT | 51666 |
rs560845400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95493733 | ACTATAACCAGTTTC[A/G]TGTTCTCAGTGTTTA | 51666 |
rs560864221 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95531278 | TCTTACCTACATCTT[A/G]CTAAGGGCTGGTCAT | 51666 |
rs560886064 | snp | C/T | | | | | GRCh38.p7 | 7:95466396 | GTTTAGATTTATGGA[C/T]TATTCAAATATATTT | 51666 |
rs560898264 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95530180 | ATAAGGATGTGGGGG[A/G]CTGGGTGCAGTGGCT | 51666 |
rs560976733 | snp | G/T | | | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95474548 | TCTTTTTGAGACAGG[G/T]TCTCATTCTGTCATC | 51666 |
rs561081117 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538133 | GTAATATGTTTACAT[A/T]CTCATTCAAATGGCC | 51666 |
rs561116844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95516729 | AAGCATTTATAAAGC[C/T]GAGCTGTTTTCCTAT | 51666 |
rs561239741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95509417 | CATGGTGACCAACGC[C/T]ATGTCTCCGGGCTCA | 51666 |
rs561241204 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95494940 | TCATTTATGTATGGC[G/T]TGTAGACATAGTTAA | 51666 |
rs561297692 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95494296 | TATTCTAGATTTCTT[A/C]TGACCTTATCTAATC | 51666 |
rs561341718 | in-del | -/TTCTTTTC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515361 | TTTCTTTTTCTTTCT[-/TTCTTTTC]TTTCTTTCTTTTCTT | 51666 |
rs561370262 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472995 | CAGCAGTTTGGCAGT[A/G]GAATAAATGATTGCT | 51666 |
rs561455330 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95464788 | TTTTAAATGCATTCA[C/G]AACTCATTTAAATGA | 51666 |
rs561617204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95501313 | GGGGCCATGCCTTTT[A/G]AAAGACTGTTCCCTG | 51666 |
rs561624784 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95529713 | CTACAAATGATTAAG[A/G]TGAGGAATAGAATAA | 51666 |
rs561631291 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ASB4 | GRCh38.p7 | 7:95508574 | TGATGTTTGCCTTTA[A/T]GATGCTACTAGTCTT | 51666 |
rs561638763 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95518989 | TTAAAGAATGAGGTG[C/G]ACAGGTGAGGAATTA | 51666 |
rs561692848 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASB4 | GRCh38.p7 | 7:95532699 | AGAAGAGAGGCAGGA[A/G]GACTTACCTTGAATC | 51666 |
rs561784340 | snp | A/C | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95483274 | TGCTATTCACTTGAT[A/C]CACGTGGTCTGGCCA | 51666 |
rs561824389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95502811 | TTGAAAATATATAGA[C/T]AGGCACTTTTAATTT | 51666 |
rs561827989 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95508537 | TGGGTTTCCGAGCAG[C/T]CTGGAGGGTCCAATT | 51666 |
rs561843418 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95481996 | GAGGTGAGTTGAAGC[A/G]GTGGCTTGGATAGTG | 51666 |
rs561880816 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95525039 | ATTAACCTGGTCATG[G/T]GACAAGAACCCAGAT | 51666 |
rs561896503 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95526952 | AAAACAAAATTCACT[G/T]AAGTTTTCTAGTCTG | 51666 |
rs561899005 | snp | C/T | 0.00358779 | 0.0422022 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95473973 | TTCACCTTCCTTAAC[C/T]GAAAATAAAGCCATA | 51666 |
rs561904482 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95489052 | TACAGCATTTTTATA[C/G]GATTTAAGAAGTAAC | 51666 |
rs561935345 | in-del | -/AAAATT | 0.00159617 | 0.0282053 | | | GRCh38.p7 | 7:95465055 | TTTCTGTTATAGGGG[-/AAAATT]AAATGACACCTCAGA | 51666 |
rs561944880 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95532161 | GAAAGTCATCTTTAC[A/G]ACAAGTAAGTGACTG | 51666 |
rs561996072 | snp | C/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95482889 | GTGGTTTAGAAACAA[C/G]CAGATATGCCTGAGG | 51666 |
rs562017335 | snp | C/T | | | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95470855 | TACTTACATGTTTTA[C/T]TCAAAATTCTTTTAA | 51666 |
rs562063490 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95489931 | AAACTGTTTCCAAAG[C/G]CTTTACCAACTTGAT | 51666 |
rs562082838 | snp | C/T | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473600 | AAAGAGCCTATAGAA[C/T]ACAGATGCCATTGTG | 51666 |
rs562087167 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95534024 | TCTTAGCTTTCTAAT[A/G]GGGAGCATCTATTGT | 51666 |
rs562089935 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95520447 | TTGTTTCAGATCTCA[G/T]AGAAGGCTTGGCTAA | 51666 |
rs562125172 | snp | A/G | 0.000399281 | 0.0141238 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95474383 | CAAAATTTACCAAAA[A/G]GGATCTTGCTCACTT | 51666 |
rs562128917 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95466280 | GTAATGAGATGGGGA[A/G]TTGGGTTTAAAAGGT | 51666 |
rs562166806 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513945 | GAAGGATTTCGATGC[C/T]GGCATAAATTACCAG | 51666 |
rs562177893 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95477080 | GTGGTTTAACCTGGA[C/T]CACGTTTTATCCGCA | 51666 |
rs562189029 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95473930 | GAAGGAACCGGATGG[C/T]TTTGGGGACATTTCT | 51666 |
rs562196753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95521271 | GAAAAGCCCAACCCA[A/G]TGAAAAATGGGCAGA | 51666 |
rs562256770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95527602 | CCTGGGTACCTTTGC[C/T]GGTTGTCCAGGAGAT | 51666 |
rs562403859 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95540089 | TTCTTATTCACCTTG[C/G]TTGTGCTTAAACACT | 51666 |
rs562403949 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASB4 | GRCh38.p7 | 7:95533562 | CATCTCTTGATCTTC[A/G]TGACCCCCTTGATAA | 51666 |
rs562404722 | snp | A/G | | | | | GRCh38.p7 | 7:95479715 | CCTACTATGTATCAG[A/G]CCTAGAACACAGCAG | 51666 |
rs562423056 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASB4 | GRCh38.p7 | 7:95517705 | TAATCAATTACAGGC[C/T]ACTAGTGATCTTCGT | 51666 |
rs562423811 | snp | A/C/T | 0.00199529 | 0.0315338 | intron-variant | ASB4 | GRCh38.p7 | 7:95497313 | AGATGGTGGCTTGCA[A/C/T]CAGGGGCAAGCTCAG | 51666 |
rs562510813 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95524108 | AGATATGCATACCCA[G/T]TGACCCAGCAATTCC | 51666 |
rs562534305 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538091 | ACCCAGGTTTTCTTC[C/G]AACCAATATAATTCT | 51666 |
rs562574830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95489876 | TTCTATTGGTTTTCA[C/T]TGGTTACTTCCATAC | 51666 |
rs562597688 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95481426 | AGAAGTATAACAGAT[A/G]AGAAGAAAGGGATGT | 51666 |
rs562623403 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95519565 | GGTGATGAGAGCAAG[A/T]GTAAACCAACATGGA | 51666 |
rs562647491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95509808 | ATCCTTGCAACAACC[A/G]TGTGAGGTTGCACAT | 51666 |
rs562664664 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95488166 | CTAACACGGTGAAAC[C/T]CCATTTCTACTAAAA | 51666 |
rs562668879 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95532059 | GGCCCCCCTCCAAAG[A/G]AAAAGTAAAGAAAAA | 51666 |
rs562686322 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95526159 | AATAGAACAGTGATA[A/C]GGAATTTCGAAGCCA | 51666 |
rs562697059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95533528 | TTCTAATTCAATCTG[C/T]TGGTATTTAATCTGT | 51666 |
rs562701363 | snp | C/G | | | | | GRCh38.p7 | 7:95460420 | TTTGACCAAAATGCT[C/G]ATAGTGATATGGACA | 51666 |
rs562732841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95525927 | TGAGTTTGTATAGGA[C/T]ATTGAGCATGCTTGT | 51666 |
rs562761650 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539302 | GCAATCACCTAACTG[A/G]TTAATCTCAGTTGAG | 51666 |
rs562833450 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95489504 | GTTATTTTAAGCTTC[A/G]TAATAAAATCTGCAG | 51666 |
rs562982332 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASB4 | GRCh38.p7 | 7:95506521 | CATGAATTCTACCCC[C/T]GACTTAGAGTAGAAT | 51666 |
rs563045574 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95533921 | TGTAGGTAATGATCC[C/T]CTATCTTTTCCATTT | 51666 |
rs563111966 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95520387 | GTTTATTGGAAAGTA[A/T]ACAAACAAGCTCAAC | 51666 |
rs563206160 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95503372 | GTTTTCTTTCCTTTG[C/T]ATTTTTATGCCTCAG | 51666 |
rs563265441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95505505 | ATTCCTTCTTCAGAG[A/G]CAACCACTTTTACTT | 51666 |
rs563456545 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95468915 | AAAAATTTTAAAAAA[C/T]CAGTGCTCTTAGAGT | 51666 |
rs563521750 | snp | C/G | 0.00279162 | 0.0372561 | | | GRCh38.p7 | 7:95468152 | TTGGGTTGGGGGGGG[C/G]CCCATTCAACCTAAA | 51666 |
rs563546504 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95460582 | GACAGAGATGATTTA[A/G]GGTATCTGGTGGAAG | 51666 |
rs563547244 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95475963 | ACTTTTCGGTCTCTA[C/T]ATATCAAGATCCCAA | 51666 |
rs563640508 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95486815 | GTCTTATAACGACCT[A/C]AGGAAAACAAAAATT | 51666 |
rs563641793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95522717 | AGGAAGGGGTCTCCA[C/T]CTTCTCTGCTGAAAT | 51666 |
rs563765571 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484257 | GGATGGCTTGAGCCT[C/G]AGAGGCAAAGGTTGC | 51666 |
rs563779246 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95514937 | AAAAACTTCCCTCTT[C/G]AATTCACCTAAGGGG | 51666 |
rs563863229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95535249 | CTATGGAGAGAAAGT[C/T]GGTTTTGTGATCTTT | 51666 |
rs563873579 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95534009 | CACATAATAACTCCA[A/T]CTTAGCTTTCTAATG | 51666 |
rs563891159 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95526068 | AATGTTATCTTTCTA[C/G]TACTTTCTGGTTTTC | 51666 |
rs563900911 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95509584 | TAATTTAATATCTTT[A/G]TGCGTCAGTCCTCCT | 51666 |
rs563953162 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASB4 | GRCh38.p7 | 7:95533400 | TGTGACACCAAGGGT[C/G]TTAAAGATGAGGACA | 51666 |
rs563953589 | snp | A/T | | | | | GRCh38.p7 | 7:95477158 | CGGGTTCATTTATCG[A/T]GGAACACTGCCATCA | 51666 |
rs563953898 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95522314 | ATTCATGATGGCAAT[G/T]ATGCTCGTGGTGTTT | 51666 |
rs563955195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95525627 | GCCTGTAAGAATTTC[A/G]TCCTGACCCTTTGAT | 51666 |
rs563969298 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95477996 | GAATTAGATACTTCC[A/G]TAGTATAAAATAAAA | 51666 |
rs564029222 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95502520 | GCTGTCATTTACTTA[A/G]GGCCTCAAATTCAGA | 51666 |
rs564083657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95512329 | TACCAAATGGGGCTA[C/T]GGATAATTCAAGTTG | 51666 |
rs564101477 | snp | C/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95460447 | GACAATGAAGTCCAG[C/G]CTGAGGTGGCCTCAG | 51666 |
rs564122819 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469883 | AAAATACTTAAATGG[C/T]GGATTTTCATATAAA | 51666 |
rs564168841 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95497411 | TTGGATGTGGGTGGG[C/G]TGTGAAGGAAAAAGG | 51666 |
rs564208560 | snp | A/G | 0.000798403 | 0.0199641 | nc-transcript-variant, splice-donor-variant | LOC107986823 | GRCh38.p7 | 7:95470935 | TTCCCTGTTTACAAA[A/G]TAAGTTTAACTTTTA | 51666 |
rs564212122 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95531227 | CCTATCCTACATCTA[C/T]ACACATCTCTCTCTT | 51666 |
rs564225808 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95505741 | TGATGTTATATTATA[A/G]CTATGAGGCTTGTGG | 51666 |
rs564277718 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95521351 | TATGAGAATACACTT[C/T]ACTGGTAATCAGGAG | 51666 |
rs564315175 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95482692 | TCAATAGGCTTGCTG[A/G]CGTAGGGAGAAAAAG | 51666 |
rs564337017 | snp | C/T | | | | | GRCh38.p7 | 7:95466870 | TATTGTGAGACTTAT[C/T]CACTATCATGAGAAC | 51666 |
rs564393517 | snp | A/C | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95461460 | TGGCCAATTTCTCCC[A/C]TTTGGAATGAGTGTA | 51666 |
rs564396616 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95476271 | TATGCAGCGGCAAGG[C/T]TTCCAGCCCAGCCCA | 51666 |
rs564469931 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95513442 | GAGACCTAGGGAATA[C/G]ATACAGTCTGTTGCC | 51666 |
rs564489685 | in-del | -/T | 0.0252325 | 0.109451 | intron-variant | ASB4 | GRCh38.p7 | 7:95507218 | ATAGTCTCTTATGAA[-/T]TTTTTTTTCCTTGAG | 51666 |
rs564530361 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95540117 | ACTTATGTTCATCTA[A/G]TGTAGAATACATGGC | 51666 |
rs564560785 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95490683 | ACATCCTCTCCAAAC[A/G]CTGGAGCAGAACCAA | 51666 |
rs564569001 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95516922 | GGTGTTCACTTTCAG[C/T]TTGGTATCTCTAGCT | 51666 |
rs564589229 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95514003 | CCTCCACAATTCTAA[A/C]AATCTGCATTTCACT | 51666 |
rs564608795 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95507838 | AAGTGTTAAATACTA[C/T]GGAGAGATCCAGTAA | 51666 |
rs564646295 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95483536 | TCTTTTTGCCACTGA[G/T]TTAGGTGGGGAGACC | 51666 |
rs564696259 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ASB4 | GRCh38.p7 | 7:95540657 | ATCTACTGTCTTGAA[A/G]AAAAAAACAATCTCT | 51666 |
rs564711243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95506542 | AGAGTAGAATTCTAG[A/G]TTCATAAACATTTTC | 51666 |
rs564730764 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95535335 | CTTTGGAGAAAGTTG[G/T]TTAAGTGCAGAGGCA | 51666 |
rs564746825 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95491485 | CCTGAAGTCTGCAGA[G/T]GTGAGCAGAGGGGGG | 51666 |
rs564788850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95486335 | ATTGTGGGCTGATAT[A/G]TATGTATAAGTCGTG | 51666 |
rs564824464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95490957 | ATCATAGACGGCTAT[C/T]TAAAGATTTGGGGGC | 51666 |
rs564835217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95499437 | AAGGACAAAGAAAGA[A/G]GTAGTAGGTTCCAGA | 51666 |
rs564930092 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95479090 | CTGTGTTCCATAAGG[A/G]AGAAAAAAGCCCTAA | 51666 |
rs564931577 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95492963 | ACATAACTCAATAGA[A/C]ATGTATAAATGAATC | 51666 |
rs565033608 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95492260 | ACTCACATAATACAC[A/G]AACAGGATAGAGTCT | 51666 |
rs565090650 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95523567 | CTGCTTAGTGAGGTA[A/G]TTAGTCTTATGCATC | 51666 |
rs565098847 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95517512 | CAAAGTGAGGCAAAA[A/G]TTTAGGGAGTGAGAA | 51666 |
rs565161084 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95489205 | AATTTACAATCTACT[G/T]GGCACACCAGTAATC | 51666 |
rs565180241 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95489938 | TTCCAAAGGCTTTAC[C/T]AACTTGATCTTCCTT | 51666 |
rs565290350 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASB4 | GRCh38.p7 | 7:95515256 | TTCTTTCTTTCCTTC[C/T]TTCTTTCTTTCTCTT | 51666 |
rs565337596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95534268 | GAATCGCTTGAACCC[A/G]GGAGGTGGAGGTTGC | 51666 |
rs565387494 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95501197 | CCCACTTTACTCTGC[A/C]TGAAGCAAATCCTGA | 51666 |
rs565462010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472130 | CTAGGTGGGGGCTCA[A/G]TAGCTCATGCCATTT | 51666 |
rs565502041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95504846 | CAGAAGACTTGCCTC[C/T]AATCATTCTGCTCTG | 51666 |
rs565514422 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539817 | TGGGTGCACTAAAAT[A/C]TCAAAATTCACCACT | 51666 |
rs565522297 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471678 | TCTTTTCTCATAAAG[G/T]AATGCCCTTACATGA | 51666 |
rs565524311 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95479899 | ATGGCTTCCTGGTGT[C/T]CCTTCCTGTTTCTTG | 51666 |
rs565527599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95527351 | AACTTTTAGGTTTAT[C/T]TGCTATGAAAGAGAA | 51666 |
rs565542852 | snp | A/G | 0.0142736 | 0.0832652 | | | GRCh38.p7 | 7:95463688 | CCAGCCATGCTTCCT[A/G]CGCAGCCTGTGGAAC | 51666 |
rs565546567 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASB4 | GRCh38.p7 | 7:95522064 | TTGACTATTTCATAA[C/T]TCATTAAAGTCTTAG | 51666 |
rs565555483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95507857 | GAGATCCAGTAAGTT[A/G]AGAGTTAAACAGCTG | 51666 |
rs565592991 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469486 | ACCTACATGTGACAA[G/T]GTAAAATGTTAAATG | 51666 |
rs565602760 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ASB4 | GRCh38.p7 | 7:95540255 | TGTTTACTTACCAAT[A/C]AGACTCTTTTTCCTA | 51666 |
rs565656082 | snp | A/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95476518 | TACCCCCTGGAGCAA[A/T]CAAGGGGCAGCTACA | 51666 |
rs565664103 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95520933 | TTATTCTTTTTTAAT[G/T]TTAAGAAAATTTCTT | 51666 |
rs565702542 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ASB4 | GRCh38.p7 | 7:95496866 | ACAAAAAACAAAGAA[A/C]AAAAACAAACAAAAA | 51666 |
rs565735423 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95477632 | TAGGTTGGAGACTTC[A/G]CTTTGCGACTAATTA | 51666 |
rs565797761 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484298 | GATCACACCACTGTG[C/T]TCCAGTCTGGTGACA | 51666 |
rs565953611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95490819 | AAACACACACGCGCA[C/T]GCGTGCACACACACA | 51666 |
rs565981943 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95490321 | CTTTCCCATTTCCAT[C/T]CTAGGGTTCTTTTCC | 51666 |
rs566030510 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95493268 | GAAATAACTGGATTT[A/C]TTTTTAAAGAGGAGA | 51666 |
rs566039532 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95499125 | AGAGTTTTCATATCT[C/G]TTTGAAACTTCAGTG | 51666 |
rs566085116 | snp | A/G | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484104 | TGGCTGAGGCAGGAG[A/G]TTCGCTTAAACTTAG | 51666 |
rs566104535 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95522124 | AGATGCAGTAACACA[A/G]CAGAGTTCTCTCTTT | 51666 |
rs566165431 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95524224 | TGGGATAGCCTGACA[C/T]GGGCAATGCCCATCT | 51666 |
rs566166682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95492461 | ATGAAAACTGCATTG[C/T]GGGTATTCTGAGTCC | 51666 |
rs566216770 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95500659 | GCCCAGCATATTCTC[A/C]TTCTTCTTTGGTTCA | 51666 |
rs566238288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95513607 | CTAGAAAAACAACAT[C/T]ACAGAAACATCCAGA | 51666 |
rs566241785 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95461761 | TTCTCATAAACCCCA[C/T]GTGTCATGGAAGGAA | 51666 |
rs566277211 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95521640 | CTTCATAAAGGAATA[A/G]CTAAACTGTGGTTTA | 51666 |
rs566304056 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95470509 | AAGAATGAACAAACA[A/C]TTGTAGACAGGGCCA | 51666 |
rs566313586 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95503475 | TGGCTCCAGAAGCCC[C/T]GAGTGCATGGATGGG | 51666 |
rs566362867 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95506833 | CCTGAATTATTTCCT[C/G]GGTGAGTTCTTTTCT | 51666 |
rs566378888 | in-del | -/TG | | | intron-variant | ASB4 | GRCh38.p7 | 7:95527194 | GTGTGTGCATGTGTA[-/TG]TGTGTGTGTGCATGC | 51666 |
rs566384889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472446 | TGTGTGGAATTCTGG[A/G]CAATTTGTACACACT | 51666 |
rs566424140 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASB4 | GRCh38.p7 | 7:95506152 | GATCCTCCTGCCTAG[A/G]CCTACAAAGTGCTGG | 51666 |
rs566425975 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95514191 | CTCTCACCCTCTCTT[A/C]ACGTCATTTCTTTCT | 51666 |
rs566477293 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASB4 | GRCh38.p7 | 7:95515407 | TTTCTTTTCTTTTCT[C/T]TTTCCTTTCTCTCTC | 51666 |
rs566521485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95532275 | GCTGAAGATGTTTTC[C/T]TCCAAATACAAAGCC | 51666 |
rs566532822 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95531791 | CTCCTCTCAACATGT[G/T]CTCTTGGTCCAGCAT | 51666 |
rs566573573 | snp | C/T | | | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471229 | CACGTCCCCTTCAAA[C/T]GATGTGGCTTGCCCC | 51666 |
rs566643103 | snp | A/G | | | | | GRCh38.p7 | 7:95464500 | TAATGCTTAAACATC[A/G]CCCATATTTTGTAAT | 51666 |
rs566674351 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95529119 | AGACAAGCAAATAAA[A/G]GGGTAATTTTAATAT | 51666 |
rs566818533 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95489668 | GTAAGCCAAAATTGC[A/G]TTTACCAGATGATCA | 51666 |
rs566827194 | in-del | -/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95495754 | TTTTTTTTTTTTTTT[-/T]CAGGTTACTGGTTGC | 51666 |
rs566849586 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95487985 | TACTCTGTTTAATAC[A/G]CACATGGGCACAAGG | 51666 |
rs566874167 | snp | C/T | | | | | GRCh38.p7 | 7:95461235 | AAAAGCCACAGACAC[C/T]CAATGCCAGCCCATG | 51666 |
rs566879023 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95525169 | AAGGTAGGAGAGAGG[A/T]CTGAGGCAGATTCTC | 51666 |
rs566883723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95523196 | ATAATTAATCAAGAT[C/T]GTTATGCAACTTCTG | 51666 |
rs566914662 | snp | C/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95465818 | GTAGTCCTAGCTACT[C/T]GGGAGATTGGAGTAA | 51666 |
rs566945691 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95522555 | TTATTTTTAAAAGAT[C/T]ATGTGTAGATGATAC | 51666 |
rs566991407 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473487 | TCCCAGCGGAGCCTG[G/T]CTGGGTGTGCAGCTG | 51666 |
rs566993088 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95481564 | ATTCTAGCTGGCTTC[A/G]AATTTCTTCCCTATG | 51666 |
rs567049145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95487758 | ATTGAGGTGTTTTCA[C/T]AGTGTTAGGACTGTG | 51666 |
rs567151111 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484492 | ATTACATGAGTTTGT[G/T]CACTAAAAATTTGAC | 51666 |
rs567320199 | snp | C/G | 0.000131887 | 0.00811949 | missense, intron-variant | ASB4 | GRCh38.p7 | 7:95537674 | GAACATTACACAACA[C/G]ATGCCATAGAGCAAT | 51666 |
rs567332113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95507404 | GAGCAAACTTCTACT[C/T]CTGTGCGAAGTCTTA | 51666 |
rs567332894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95536988 | TACAGAAAACCATTG[A/G]CAGAGTCAAGTTCTC | 51666 |
rs567435117 | snp | G/T | | | missense | ASB4 | GRCh38.p7 | 7:95486082 | ATTGAAGGCTATTTT[G/T]ATCCAAAGGCAAATA | 51666 |
rs567577566 | snp | G/T | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95537831 | CACAGTTTGCCTAAA[G/T]AAAATGGTACTTGGG | 51666 |
rs567587314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95528930 | CACAGTGCCAGTGCC[A/G]GGATTCAACCTTAGA | 51666 |
rs567684386 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95506856 | TCTTTTCTTCTGCTT[C/T]CTATATGCTCTCTTT | 51666 |
rs567702692 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472718 | GTTAACTACAAGGGA[A/G]CTTCTTTGCAGTATG | 51666 |
rs567718250 | snp | A/T | | | | | GRCh38.p7 | 7:95482026 | GGAGGCAGGTCTCAC[A/T]CCTGCTATTAGCATT | 51666 |
rs567724577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95507888 | CTATTGGATTTAGTG[A/G]CATGGATGGAACTGA | 51666 |
rs567762223 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95480282 | CCTTGTAGCCCCTCC[A/G]CTGGTATAAAAGCTC | 51666 |
rs567803474 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95488641 | AAGTTTGTGAGACTT[G/T]ATTAAATCAAAGGAG | 51666 |
rs567868609 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95500484 | GGCAGGAGAATTGCT[G/T]GAGCTCACGAGTTTG | 51666 |
rs567892424 | snp | A/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95465513 | CTTAAAAAAAAAAAA[A/T]TTCTGAGACAGGGTC | 51666 |
rs567928934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95502196 | AAAAAAGAAAAATCA[C/T]ATAAACAGCAAATAA | 51666 |
rs567946132 | snp | G/T | | | | | GRCh38.p7 | 7:95479615 | TTTTGTGTTAAATAT[G/T]GAATATCCACTGATA | 51666 |
rs567952879 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ASB4 | GRCh38.p7 | 7:95493934 | CTCCTATCAATTAAC[A/T]TGGAGGTTGTTTAAC | 51666 |
rs567961119 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95493543 | TTTTCCCCTCTGGAC[A/C]GAGAGACAATAGCTT | 51666 |
rs568127487 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538463 | TCACCATTTAGCAGA[A/G]GATCCAGACATACAC | 51666 |
rs568140507 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95518646 | AGATAAGGGTAAGAT[A/G]GAGATTAAACTGGGT | 51666 |
rs568143208 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95499786 | GAAAGAAAACAGCTG[A/C]AGATGCACGAGACAG | 51666 |
rs568320459 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95510580 | TTTTTTCTCCAAACA[C/T]TAATTGTTTTGGTCT | 51666 |
rs568339549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95509910 | TCAGATTCAAGCAGA[C/T]CAAATTTTATTTGTT | 51666 |
rs568381128 | snp | C/T | 0.00835141 | 0.0640778 | | | GRCh38.p7 | 7:95475810 | TATCTTTTAGTAAAA[C/T]TAGATGGCCATTCTC | 51666 |
rs568403046 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95508985 | CAGTCCAGGTATGAC[C/T]GTGGGTTGGAGTCAT | 51666 |
rs568404302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95519726 | CTGACCTGTCTTAAT[A/G]CCTTTTCTAAGAAAA | 51666 |
rs568411499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95517741 | CAGTTCCAGTGGAGT[A/G]TGGGGACAGAGGCAA | 51666 |
rs568438813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95504101 | TGAATAAAGAGAGTC[A/G]GGGCAGGTTTAGGTG | 51666 |
rs568480475 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95500730 | CATCTCATCTCAACT[G/T]CTGAAAGACTGGAAC | 51666 |
rs568494898 | snp | A/G | 0.00358779 | 0.0422022 | | | GRCh38.p7 | 7:95466738 | GACTAACAATTCCAC[A/G]TGGCTGGGGAGGCCT | 51666 |
rs568531573 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95496664 | CCAGTCTCGGCAACA[G/T]AGGGAGACCCCATCT | 51666 |
rs568550769 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95533210 | AGGGTATAAATTCAG[A/T]TTGGGGGTAGAATGT | 51666 |
rs568557708 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95465172 | GACTTTATACCTAGC[A/G]TTTCAACATACAGAA | 51666 |
rs568560555 | snp | C/T | | | | | GRCh38.p7 | 7:95467173 | CAAAGAAATACTAAT[C/T]TCAACAAAAATATAT | 51666 |
rs568595543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95494628 | TCATCTTCTTGCCCT[C/T]AGTATTTTTTCTTTC | 51666 |
rs568641190 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95532431 | GCGTAATTCAGAAGA[A/C]AGTGACACCCCAGGG | 51666 |
rs568686607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95525759 | GCTGACCTGAAATAA[A/G]ACCTGACCCAGAACT | 51666 |
rs568717255 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95508836 | AAAGAGAACACAGAG[A/G]GGGATCTGATGGAGT | 51666 |
rs568749361 | snp | C/T | 0.00557542 | 0.0525036 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471896 | AACAGATGAAGAAAC[C/T]GAGCCACACAGAGGT | 51666 |
rs568772101 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95464254 | GTTGAAAGCTAACAC[A/G]TAGCCTGCACCATTA | 51666 |
rs568792000 | in-del | -/TT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95519859 | TTTTTTTTCATTGAC[-/TT]TAACTCACTTGATAA | 51666 |
rs568836011 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472518 | TGTGATTCCTGTGGA[A/G]CTGCAGTGCTATAAA | 51666 |
rs568868650 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95525689 | GAAGTGACCCTGCAC[A/G]TGGCTTCTGGGAAGA | 51666 |
rs568880843 | snp | A/G | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95485026 | TATATATGTGTATAT[A/G]TGTATATATGTATAT | 51666 |
rs568941191 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95486870 | ATTTTCTGGAACCCA[C/T]GCTTAATAAATCAGA | 51666 |
rs568990719 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95492500 | GGATTGAGGCAGGCA[A/G]CTCATGGCTCTAGCA | 51666 |
rs568995146 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95480222 | GGTAGCACATATTAC[C/T]ATGTGACAAACTATA | 51666 |
rs569048405 | in-del | -/TGTG | | | intron-variant | ASB4 | GRCh38.p7 | 7:95492994 | TATATGTACATACAT[-/TGTG]TGTGCATATCAATTT | 51666 |
rs569053839 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95518600 | TAGACTATATTGGCA[C/T]TCAAGAAAGAGTTGA | 51666 |
rs569113636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95508168 | GACAGTAGGGATAAT[C/T]TTTGGTGTGAGGATT | 51666 |
rs569148736 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95499966 | GCAAGCTCTGCCTCC[C/T]GGGTTCACGCCATTC | 51666 |
rs569176371 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95516318 | TCTTATCTATGGTTA[C/T]TTTGCAAAATTTTAA | 51666 |
rs569233040 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95511221 | GACCCCTCTCTTTTC[C/G]AAGACAAAACATTTT | 51666 |
rs569263668 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515187 | TCTTTCTTTCTTTCT[C/T]TCTTTCTTTCTTTCT | 51666 |
rs569271613 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95482161 | CAGGTAAAATAATCA[A/G]TTGATTTTTAGCAGA | 51666 |
rs569322124 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539753 | AGCTTGAGAGTGGGG[C/T]GAGGGATAAAAGACT | 51666 |
rs569375507 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95510206 | TGTCGATGTTTCTTC[C/T]GAAATGAGTCCCATC | 51666 |
rs569423549 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95506001 | CAGGCTCAAGCAGTC[C/T]TCCCACCTCAGCCTC | 51666 |
rs569428718 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95531977 | ATTTAGGATAGAGTT[G/T]GCTACTGGTAGATGG | 51666 |
rs569440979 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95537858 | TGGGTTGATTATAAC[A/T]CTTCAGGGATTTCAA | 51666 |
rs569458495 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95488506 | TCTTAAGTCATAAAG[G/T]CATTGTCAGGCAACA | 51666 |
rs569719663 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95503077 | TTATATGTGACTATG[A/C]ATATCAAAATAATAT | 51666 |
rs569728899 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95483635 | TATTTGCAGCTTTGT[A/G]ACAAATTCTAGTGTA | 51666 |
rs569764255 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95461538 | GCTTTTGATTTAACA[A/G]GCTCATAGGCAGAAG | 51666 |
rs569792958 | in-del | -/TG | | | intron-variant | ASB4 | GRCh38.p7 | 7:95537090 | TTAGATGTCAAAGTC[-/TG]TCTGTAACACATGGA | 51666 |
rs569799023 | snp | G/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95459585 | AAGGAGCACCTTCTT[G/T]TTACTGTGAAGAGCA | 51666 |
rs569807941 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95491537 | GAATAAATCACATTC[G/T]AGGTTTCGAAGCCCT | 51666 |
rs569850397 | snp | G/T | 0.00159617 | 0.0282053 | | | GRCh38.p7 | 7:95459967 | TGATGGTGAGTTCTC[G/T]TGAGATCTGATGGTT | 51666 |
rs569938125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95503886 | CTCTTAAAGGATTTT[C/T]CCCTATTTTTTCAGT | 51666 |
rs569976759 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95460989 | TTCAGAGGGTGCAAG[C/T]CCCAAGCCTTGGCAG | 51666 |
rs570038669 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469237 | ATTATAAAACAACTG[A/G]CATGCAGACAATTTT | 51666 |
rs570072726 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95530018 | GCCTTCATGAAAGAT[A/T]CTTTCTAGTGGGAGA | 51666 |
rs570081636 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95496542 | TATGCTAGGTAGGCT[A/G]AAATTTTAAGAATGA | 51666 |
rs570140080 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95498361 | ATGTCCCTCTACTGG[C/G]GGGTAGATCATTAGA | 51666 |
rs570140580 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95499444 | AAGAAAGAGGTAGTA[G/T]GTTCCAGAAGCAGAG | 51666 |
rs570142450 | snp | A/G | | | | | GRCh38.p7 | 7:95468783 | CCTGTTTTTAGCATT[A/G]TTCTTACAATAAGTA | 51666 |
rs570207362 | snp | C/T | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95483717 | GAGCTAAGTTACACA[C/T]GGGCAGGGATTTCTG | 51666 |
rs570208350 | snp | A/C | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95482385 | AAAGCAATGCTTTAA[A/C]ATTTCATTCTGAAGT | 51666 |
rs570232684 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95505109 | TCCTGGAGGTCCTAA[A/C]TGGCACAAAGAGAAG | 51666 |
rs570252269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95527180 | CTAAAGTCGTGTGTG[C/T]GTGTGCATGTGTATG | 51666 |
rs570259145 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95532414 | GATTTTTTTTTCTCC[C/G]AGCGTAATTCAGAAG | 51666 |
rs570316314 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95526486 | AATAAATCTGCCTTT[A/C]TTTACCTACAACTGT | 51666 |
rs570326706 | snp | G/T | 1.64925e-05 | 0.00287158 | missense | ASB4 | GRCh38.p7 | 7:95495821 | TCCATCTCTCTGTCT[G/T]GTTTGGCCATGTGGA | 51666 |
rs570408275 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASB4 | GRCh38.p7 | 7:95521493 | TGATATATACACTGA[C/T]GAATATAATTTAATA | 51666 |
rs570495169 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539651 | AAAGTGAAATACCAT[A/G]TGTTCTCACTTATAA | 51666 |
rs570525272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95489976 | ATGAGCTTTTGCTCA[C/T]AAATGATACAGGCAG | 51666 |
rs570528329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95533270 | CATATGTAATCTATT[C/T]TATCAGTAGTAAAGA | 51666 |
rs570564488 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95518014 | ATGATCAATTGCAAA[A/G]AGGAAGGTGTTGGTC | 51666 |
rs570568984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95517800 | GGTGAGACAGTGGAT[A/G]TGGAAAACAGAGACC | 51666 |
rs570594614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95497727 | CAACCACTGATGTTT[C/T]CTGTCCCTATAATTT | 51666 |
rs570620084 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95510173 | TAGAAGTGTGTTTAA[C/T]GAAAAGATATGAAAA | 51666 |
rs570627221 | snp | C/T | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484706 | TTTGACTTCCACAAA[C/T]GACATATAAAAATGC | 51666 |
rs570628431 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95525271 | GAATAAATTTCAGTT[A/G]TTTTAAGCTACCCAG | 51666 |
rs570695465 | snp | C/T | 0.00199481 | 0.0315187 | | | GRCh38.p7 | 7:95477351 | AAAGGGTCAACTCTA[C/T]GTCACCTTTTGAATT | 51666 |
rs570744462 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95482978 | AACTCCATTCCTTAG[C/T]TTAGGTTCATGTCTA | 51666 |
rs570783479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95512615 | TTGTAAAGATACAAA[A/G]GTACATAAAATCTAC | 51666 |
rs570802545 | snp | A/C | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:95460154 | CAGCCTTGGGTATTT[A/C]TTCACAGTAGCATGA | 51666 |
rs570806027 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95460878 | GTGTCCAGGGCCCCC[A/G]TGCTCTGTGCAGCCT | 51666 |
rs570808372 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASB4 | GRCh38.p7 | 7:95502294 | TTTGTTGTTGTTTGT[C/T]ACGTTAATAAGCATA | 51666 |
rs570840688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95520762 | GCCACACCTGTCATT[A/G]CAGATGCTTTCTGTA | 51666 |
rs570946766 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95492232 | AAACTGACTGAGAGG[A/C]CAAGGATGACTGACT | 51666 |
rs571013352 | snp | C/G | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:95468362 | TAAAGCATGTGGGGG[C/G]GCCTCTTCTATGAAC | 51666 |
rs571041750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95522361 | CACCTCTATCAGTTC[A/G]AATATGTAGCTGTTC | 51666 |
rs571048875 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASB4 | GRCh38.p7 | 7:95526447 | GTTGCAACTTTGCAA[C/T]GCATTTTCATACATA | 51666 |
rs571062711 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95525882 | CAGAGTTTACAGAGC[A/T]ATGTACTCTTGGGTA | 51666 |
rs571082466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95498297 | GCAACATCAGTTTGC[A/G]ATCATTACAAACATA | 51666 |
rs571087357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95519883 | CTTGATAATTGGTGG[A/G]TGGTGAATATTTTAA | 51666 |
rs571285835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95513831 | CACCCTAGGCATCCT[A/G]GGCATTACTATCTGC | 51666 |
rs571295080 | snp | C/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95477695 | ATGGCCTCAGTACTT[C/T]TTTTCTTAAATGAGA | 51666 |
rs571323591 | snp | A/G | 0.000399281 | 0.0141238 | nc-transcript-variant, intron-variant | LOC107986823 | GRCh38.p7 | 7:95471306 | TCCAGGGCCATTGCT[A/G]TTGTCCTCTTTCCTG | 51666 |
rs571323806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95490905 | CTTTTAGCTACAAGT[A/G]ATATCAGTTTGGAGG | 51666 |
rs571333254 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513539 | GCCCACCCACATTAA[A/G]GAGAACAATCTGTTT | 51666 |
rs571383470 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95478181 | AAGTAAAAAGAGGAT[A/G]CAAATGCTGCCTGGA | 51666 |
rs571432270 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95519148 | AGACACAAGAGAATA[C/T]ATTTGCCATAGAATG | 51666 |
rs571486290 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95534997 | TGACCTTTAGCCCTG[C/T]CCTGACTCCATCCAG | 51666 |
rs571493705 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95489805 | TGAGCCAACCACTGA[A/G]TATTTAGAGTGAAGT | 51666 |
rs571512983 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484442 | AGGGGGCTTCAGGTA[A/C]ACTTGAACTAGTCTA | 51666 |
rs571529568 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95491416 | TGGGCTTGGTTCCCC[A/G]GTTCTCCCTCACCTC | 51666 |
rs571566984 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95516531 | TCCCAAAGGATGAGA[A/C]GCAATATTCTGTGGA | 51666 |
rs571581914 | in-del | -/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95536223 | GTCTGTGGGTTCTGG[-/T]TTTTTTTTTACAGAT | 51666 |
rs571611661 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ASB4 | GRCh38.p7 | 7:95536223 | GTCTGTGGGTTCTGG[G/T]TTTTTTTTTACAGAT | 51666 |
rs571640464 | snp | A/G | | | | | GRCh38.p7 | 7:95482753 | TGGACCCTTGTAGCT[A/G]GGAAGGCTAGAAGTC | 51666 |
rs571644081 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95486673 | CAGGCACCTTCATGG[C/T]CTTCTTCATTTTAAT | 51666 |
rs571682985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95536870 | TTATATAGCATTTTT[A/G]CCAGAATATTAAAGC | 51666 |
rs571763938 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95460331 | AAAGTTTGGAACTTC[C/T]TAGCAACTTGGAGGG | 51666 |
rs571768771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95506897 | TATTATTTGGATATC[A/G]AACCTCCCTGGACTG | 51666 |
rs571778247 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95488382 | TCCAATTTTTTTCAC[A/T]TGCTTCCAACCTTAT | 51666 |
rs571802535 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95529717 | AAATGATTAAGATGA[A/G]GAATAGAATAAGAAT | 51666 |
rs571855959 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95462547 | TTATTTAGTATTAAA[A/G]CAAGAGACTTCTACA | 51666 |
rs571886004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95533380 | GCTTCTAACACTCTT[C/T]GTGCTGTGACACCAA | 51666 |
rs571886043 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95531098 | GTTATTCCTACTCAT[A/T]GCACATCACAAATAT | 51666 |
rs571954914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95499860 | GAGACTACGGGATAC[A/G]TCCTCTTTTTTTTTT | 51666 |
rs571975249 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95467938 | CATACATTTTTTTTT[A/G]AGGGAAGAAGAGAGC | 51666 |
rs571996928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95520109 | AATTTCAGTGCTGGG[A/G]CATTATATTCAATGA | 51666 |
rs572035773 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95475744 | TTCTGTCTTTATAAA[A/G]CCAAATCATGTATTC | 51666 |
rs572079674 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484100 | TGGATGGCTGAGGCA[A/G]GAGGTTCGCTTAAAC | 51666 |
rs572123414 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95468755 | CTAATGAGCAGTAAA[C/T]GCATGTCCAAGTCCT | 51666 |
rs572203857 | snp | A/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95477785 | ACAAGCAAAATTAAG[A/T]TCTTTTAAAAAGCAA | 51666 |
rs572206638 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95512227 | TGCTTAAAAGTGAAG[G/T]TTCTGGAGTAAGACG | 51666 |
rs572236945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95489700 | TTTAAAATAAAAACG[A/G]TATAAAGAAAACATA | 51666 |
rs572242297 | snp | A/C | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95475157 | TGTGTTGTAACAAGC[A/C]CACCAGAGGACTCTG | 51666 |
rs572322133 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95491613 | CTGCCTCATCAGTTA[A/G]TTGTGTTTCTAGCAT | 51666 |
rs572345727 | snp | A/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95461034 | ATGTCCAGGCAGAGG[A/T]GTGCTGCAGGGGCAA | 51666 |
rs572362760 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95483077 | TGCAGCGTTTGAGAA[C/G]ATCAAAACTGGAGTC | 51666 |
rs572373338 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95482675 | CCACCTCTGGAGGGA[G/T]ATCAATAGGCTTGCT | 51666 |
rs572382904 | in-del | -/T | 0.0372196 | 0.131242 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539067 | TCAATTTTGCTTCAC[-/T]TTTTTTTTTTGTTCT | 51666 |
rs572527572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95507078 | GGCTGTCTGCCTATA[C/T]TTAAGATCCGAGTCA | 51666 |
rs572615629 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95520363 | TTAACACTCTGTCTA[C/T]AAACTCAGGTTTATT | 51666 |
rs572638933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95505174 | GGAAGCAAAATGGCC[A/G]TTATTTAAAACAGGA | 51666 |
rs572684427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95490951 | CTTCGGATCATAGAC[A/G]GCTATTTAAAGATTT | 51666 |
rs572697238 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASB4 | GRCh38.p7 | 7:95513964 | ATAAATTACCAGTCC[A/G]AAATCACCCTCACAA | 51666 |
rs572698779 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95497868 | GACCAATAAATTAGA[A/C]CTTTTTATTGCTGAG | 51666 |
rs572702168 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95513018 | TCTCTTTAAAATCAG[C/G]GACCTTTTTTGGCTA | 51666 |
rs572943397 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95492903 | TCAAAAGCAAGCTGC[A/G]TGACATACAGCTTAG | 51666 |
rs572956345 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485468 | TTCAGATATGTATGA[C/T]AATGGTTGATTTTAC | 51666 |
rs573015942 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95533279 | TCTATTTTATCAGTA[A/G]TAAAGATGATATTCT | 51666 |
rs573018731 | in-del | -/CAGT | 0.00517822 | 0.0506191 | | | GRCh38.p7 | 7:95478430 | AAACCTTGTCTTTCA[-/CAGT]CAAAGATGACGTGAA | 51666 |
rs573090038 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95535333 | GTCTTTGGAGAAAGT[G/T]GTTTAAGTGCAGAGG | 51666 |
rs573143506 | snp | C/T | 1.67899e-05 | 0.00289736 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95536448 | GCAGGTGATACAGGC[C/T]TGCCATTCTTGTCCT | 51666 |
rs573169639 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95530593 | GGGCTAAGCATGTTT[C/G]AGGGAGAGCAAGGAA | 51666 |
rs573216635 | snp | G/T | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538294 | GAAGGCATATGAGCA[G/T]AGTCAAAACAAGGAG | 51666 |
rs573223708 | snp | C/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95463552 | GAGTTCTTACAAAAT[C/G]TGGTTGTTTAAAAGT | 51666 |
rs573407393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95508427 | GAGGTTTGAAATAAT[C/T]GTTAGAGAGGAAATA | 51666 |
rs573410427 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95537126 | TATCAGGCACAGGGT[A/G]CAAAGTTCACTGGGC | 51666 |
rs573450968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95523510 | TTCGGATTTTAAAAA[A/G]TAAGAATTTTTGCAA | 51666 |
rs573475535 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472091 | TGTGGTGGTGGGAGG[A/G]GACTTACAATATCAA | 51666 |
rs573585230 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95479761 | TGTGGGTTTAGCTTT[A/G]AGAGAATTGGACTTG | 51666 |
rs573666206 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95533637 | ATGTCTGGTGTTTTT[C/T]TGACTTTGGAGTCAT | 51666 |
rs573693583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95506938 | TATCTTGTATTGTCT[C/T]GTCTCTCCTATTTTA | 51666 |
rs573718848 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95498654 | TGGCTTTTCTTTTCA[G/T]TTTCCTAACAGTATC | 51666 |
rs573749356 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95463488 | GATTGGTTCATGGGA[A/G]CAGTTTCTAATGGTT | 51666 |
rs573754567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95491997 | ACTTCAGTATACCCT[A/G]AGCTATAGCCTGCAA | 51666 |
rs573754857 | snp | C/G | 1.64963e-05 | 0.00287192 | missense | ASB4 | GRCh38.p7 | 7:95528223 | GTCACCTCCGTGCGC[C/G]CTGCTGCCCAGCCTG | 51666 |
rs573805027 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95476924 | GTTTAATTTATGTAT[G/T]TGTTAGATACATATT | 51666 |
rs573815088 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95485374 | TCCCTGCCCCGGACC[A/G]TCTCCCCACCTCCTC | 51666 |
rs573866212 | snp | C/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95477728 | ATTTGATACCCTTAA[C/G]AAGAACCTTTTTTTT | 51666 |
rs573873999 | in-del | -/G | 0.00636936 | 0.0560724 | intron-variant | ASB4 | GRCh38.p7 | 7:95488346 | ACTCCGTCTCAAAAA[-/G]AAAAAAAAAAAGAAG | 51666 |
rs573915248 | in-del | -/A | 0.0115144 | 0.0749975 | | | GRCh38.p7 | 7:95480878 | TCATAGTAAGTTCCC[-/A]AAAAATATTTATTGA | 51666 |
rs573924614 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95504185 | AGCTGCCCGCTTTAC[C/T]CTGCATGAAGCAAAT | 51666 |
rs573950579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95523472 | TTACAGAGAAAGTGT[C/T]TAAACTCTAATAATC | 51666 |
rs573967562 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95536367 | CTGTGAATTCTTGAT[C/G]TCTCTGTGAGCAGAA | 51666 |
rs573976648 | snp | A/G | 0.0023933 | 0.0345097 | | | GRCh38.p7 | 7:95479565 | CATTGAAATCCTAAT[A/G]TGGTTTGAAAATTTT | 51666 |
rs573986114 | snp | A/G | | | | | GRCh38.p7 | 7:95475848 | TCTCTAATCCTTGCC[A/G]TGAGCTGGCAAGGTT | 51666 |
rs574059454 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASB4 | GRCh38.p7 | 7:95487170 | AATTTACTGTCCTCC[A/G]ATTGTCAGTTCTGAG | 51666 |
rs574064135 | snp | A/G | 0.000798403 | 0.0199641 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95472000 | TTCTTACTGAATACA[A/G]AGCAAAAAAACATAA | 51666 |
rs574083598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95522750 | TTATCTTATCTGTCC[C/T]GTTCATCCCATTCTC | 51666 |
rs574112798 | snp | A/T | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95483771 | AGTGCCCAGAATAAG[A/T]GTCTGACAAATGGTA | 51666 |
rs574149995 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95506060 | GCCGTGCCTGGCTAA[C/T]TTTTAAAAAATTATT | 51666 |
rs574191751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95535272 | TGATCTTTTGCTCAA[C/T]AGTAATAGGTTGAGG | 51666 |
rs574196615 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95487946 | ATGTGTAGAAAGAAA[C/G]ACACTTGAAACACAC | 51666 |
rs574222089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95515621 | GGGTTTCCCCATGTT[A/G]ACCAGGATGGTCTCA | 51666 |
rs574239361 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95529331 | GAAGAGTTTGAAGTA[A/T]ACAACAACTGACTAA | 51666 |
rs574242131 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95522818 | AAATCTGAAAATTCC[C/T]TCTTCTTTATCATGC | 51666 |
rs574248360 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95492746 | TTGCTGTTAATCAGC[A/G]GGCAAAACACATCCT | 51666 |
rs574279890 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASB4 | GRCh38.p7 | 7:95530561 | AAAAGCAGGTGCAAG[A/G]GTCCTGAGGTAGGAG | 51666 |
rs574301069 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95525549 | TCTAGTTGCACCAAC[A/G]GGTCAAAGATCAATC | 51666 |
rs574332339 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95464422 | TAAATAAATTAAAGT[C/G]ACAATTAGCAGCTTG | 51666 |
rs574342768 | snp | C/T | 0.00022605 | 0.0106289 | intron-variant, synonymous-codon | ASB4 | GRCh38.p7 | 7:95528354 | GATTCAAATGGCAGC[C/T]TTGTCTGAAATCTCC | 51666 |
rs574349833 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95531279 | CTTACCTACATCTTG[A/C]TAAGGGCTGGTCATT | 51666 |
rs574380923 | snp | A/G | 0.000115355 | 0.00759368 | missense | ASB4 | GRCh38.p7 | 7:95486062 | AAGTCCAATGACTTC[A/G]GAAAATTGAAGGCTA | 51666 |
rs574548106 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538685 | GATAGTGTGTCTTTT[G/T]GGTATGGTTTCTTGG | 51666 |
rs574679107 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95508078 | TTTTTTTTTAGATTT[C/T]AGATGATAGAAACCT | 51666 |
rs574697641 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95507721 | AAGAGTGCAGTTGAA[C/T]CAGAGCAATTTCATG | 51666 |
rs574708542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95516437 | AGCATGTCTAGAAAG[A/G]TATCCTTTCTTTAAG | 51666 |
rs574725347 | snp | A/G | | | | | GRCh38.p7 | 7:95465955 | AACAAACAAACAAAC[A/G]AACAAAAAGACAACT | 51666 |
rs574787682 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95520941 | TTTTAATTTTAAGAA[A/C]ATTTCTTTCTCATTC | 51666 |
rs574818729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95518024 | GCAAAGAGGAAGGTG[C/T]TGGTCTTAAATTGGA | 51666 |
rs574883981 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95495362 | TTCAAGACAAACTCT[C/G]AATGATTGAAAGTTT | 51666 |
rs574907908 | snp | A/G | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:95464909 | AAGGTAAGACATTTT[A/G]TGTTTATTGACAACA | 51666 |
rs574915716 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95503133 | ATTATAGCTAATGTT[A/T]AACTGTAGCTAAGCA | 51666 |
rs574935176 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95524697 | GTTAAAATCATACTA[A/G]AGTAAGGTTGTTCCC | 51666 |
rs574964583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95525354 | CATTAAAAATATATT[C/T]CAAAGTTCCCAGGAG | 51666 |
rs574969372 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95530038 | CTAGTGGGAGACAGG[A/C]AACAAACAAAACAAC | 51666 |
rs574970924 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95489068 | GATTTAAGAAGTAAC[G/T]AAATTTTATCCCTAA | 51666 |
rs574998296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95494046 | CACAGAGTACAATGC[A/G]AATGTTGTTTTTTGT | 51666 |
rs575125970 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95506948 | TGTCTCGTCTCTCCT[A/G]TTTTATGTTTTTTAT | 51666 |
rs575146652 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95517167 | TTGTAATAGTTCTAT[A/T]TTTTTTGTTGTTATT | 51666 |
rs575186695 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95463449 | TGTAATCCCCAATGT[G/T]GGAGGTTGGGCCTGG | 51666 |
rs575228635 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95534969 | CTGCCAGCTGGCTTC[A/T]TCTTACCAGCTCTGA | 51666 |
rs575240287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95486934 | AAATCAACTGGTTAA[C/T]TGGGGGAACGTGAGT | 51666 |
rs575253413 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515287 | TCTTTCTTTCTTTCT[A/T]TCTTTCTTTCTTTCT | 51666 |
rs575257654 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95517345 | GGTCTAGTTTTAATA[G/T]TTCTTTATGTATTCT | 51666 |
rs575283550 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485734 | GCTTTCGTTCATATT[A/G]ACACTATATATTACT | 51666 |
rs575303948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95515594 | CTAATTTTTGTGTTT[C/T]TCATAGAGACGGGGT | 51666 |
rs575350938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95507124 | GAATCTAATTATCTA[C/T]GTAGAGGTTTTTTGT | 51666 |
rs575428951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95524104 | TTGAAGATATGCATA[C/T]CCAGTGACCCAGCAA | 51666 |
rs575465833 | snp | G/T | | | | | GRCh38.p7 | 7:95461752 | GAATTGTAGTTCTCA[G/T]AAACCCCACGTGTCA | 51666 |
rs575491713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95507634 | CAGAGCCCAGTGCAT[A/G]GTACATATTGGGTGT | 51666 |
rs575504396 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95509353 | GCCAGAGTTAAGCAT[A/C]CCACATCCGTTGTTT | 51666 |
rs575522557 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538390 | TGAACCAGACATCAC[C/T]GAGCCAGAGACTGGA | 51666 |
rs575530082 | snp | C/T | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95470605 | TCAAGATTCTCTGTC[C/T]GCCCCCACACCTCCA | 51666 |
rs575566465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95516646 | ATGGCTTAAAAAATA[C/T]GAGTAGCTGTTAAAG | 51666 |
rs575611647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95508551 | GTCTGGAGGGTCCAA[C/T]TGAGTTTTGATGTTT | 51666 |
rs575637086 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95507486 | TTAGGTCCCAATGCT[A/G]TGTTCTGTATTCTCA | 51666 |
rs575672926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95502374 | CGCTTAATAGAATGT[A/G]AATAGGTACCAGCCT | 51666 |
rs575690513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95501880 | ATCAAGGAGAGAGAA[C/T]AGAAGTCCATTAAAG | 51666 |
rs575789306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95494792 | AAAGACCAGCTCAGC[A/G]TATAGAAGTCAGAGA | 51666 |
rs575996133 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95497827 | CTTAGCATAATACAT[G/T]TGAGATCCATCCATA | 51666 |
rs576000664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95533347 | GTCCTACACTAAAAA[A/G]GGAAAATTACTTATT | 51666 |
rs576005953 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473578 | TCTCCCTTGCTCTTG[A/C]AACCTGAAAGAGCCT | 51666 |
rs576007840 | snp | A/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95464536 | ATTAGCAAACTACTC[A/T]TTCATAGATTGGATT | 51666 |
rs576018303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472974 | CTATTTCCTCTCTCC[A/G]CGCTCCAGCAGTTTG | 51666 |
rs576035296 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95531298 | GGGCTGGTCATTCTT[C/T]ATGACGTTAGCTCTA | 51666 |
rs576102750 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | LOC107986823 | GRCh38.p7 | 7:95475051 | GCCTATAGACAAGCT[G/T]TTTTTTATGTATAGT | 51666 |
rs576105342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95518197 | CTTCCACTCCAGGCT[C/T]ATGGAAGACCACGCT | 51666 |
rs576105374 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASB4 | GRCh38.p7 | 7:95525898 | ATGTACTCTTGGGTA[C/T]CTTCCTTGGGGACTG | 51666 |
rs576117464 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95525515 | AACTCCTATTCAGAA[A/C]AGGAAACCATGTAGC | 51666 |
rs576126536 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95507929 | AATGAGTTGAGCGAC[A/G]GATGCAGAAGTCAGA | 51666 |
rs576133135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95490945 | TGTAGCCTTCGGATC[A/G]TAGACGGCTATTTAA | 51666 |
rs576142913 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538575 | TCTGACATGAAGTGT[A/G]ATTTTTCTTTTAAGC | 51666 |
rs576205571 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95460218 | GAGTGGGATGCTGCT[A/G]TAAAGATACCTCAAA | 51666 |
rs576232106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95532690 | GTTTGGATGAGAAGA[A/G]AGGCAGGAAGACTTA | 51666 |
rs576239395 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95518828 | GGGCCATCCACAAAG[C/G]TTTTGCAGGGTGACT | 51666 |
rs576266766 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95533534 | TTCAATCTGCTGGTA[C/T]TTAATCTGTCTTCAT | 51666 |
rs576268294 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95468455 | ATGCATGTAATGGAG[A/G]GAGCTTGTGGAACGC | 51666 |
rs576272244 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95495283 | TGGATTGACAACAAC[C/T]ATAGGAAAAAAGATT | 51666 |
rs576308743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95497203 | TTTCCTTTAAAGTCA[C/T]TATTCTGGAGCTATG | 51666 |
rs576337906 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95527578 | GGCACAAATCCTTCC[C/T]TCTCCTCCCCTGGGT | 51666 |
rs576344134 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95533944 | TTCCATTTATACCCA[G/T]TTAGACTGTCACTGA | 51666 |
rs576375495 | snp | A/T | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469088 | CAGATTTAAATTATA[A/T]AAGTTGTGTCTTCAT | 51666 |
rs576404476 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95481336 | TAAGCATTAACACTA[A/G]CCTATAAAAGAATAG | 51666 |
rs576433417 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95526906 | CAGCTTCTTGAGTTG[A/C]CCACTCTCACATTTA | 51666 |
rs576447831 | snp | A/G | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:95476008 | TACCATTTCCTCTGT[A/G]AAATCTTTCTTGATT | 51666 |
rs576460002 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95483249 | CGTAAGCTGCACTCT[C/T]ACTGCTGACTGCTAT | 51666 |
rs576470693 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484024 | TGTTTAACATTAAAA[A/T]GTAAAAAAAAAAAAA | 51666 |
rs576490313 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ASB4 | GRCh38.p7 | 7:95540397 | TGTTTTCAAAAGAAA[A/G]TAAAGGGTAACTGTG | 51666 |
rs576525022 | snp | A/T | 0.000798403 | 0.0199641 | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95474338 | TGTAGCAGTTGATAA[A/T]AACTTGTGTGCTTTG | 51666 |
rs576533969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95512098 | CAGGTTGCTATCTTC[C/T]GTAACACTTGATCCT | 51666 |
rs576536607 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95481772 | ACACCAGGGTCTTAC[A/G]GGCCACTTGCCACAT | 51666 |
rs576576518 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95511622 | AGCCGAGATTGCGCC[A/G]TTGCACTCCAGCCTG | 51666 |
rs576678125 | snp | A/C | | | | | GRCh38.p7 | 7:95475392 | GAATTTAATTAATTA[A/C]TTATTTTTTGAGATG | 51666 |
rs576715424 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95504186 | GCTGCCCGCTTTACT[C/T]TGCATGAAGCAAATC | 51666 |
rs576733255 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95520007 | TCATCTAAAAAACAT[A/G]CCTTGTTTGGAGATG | 51666 |
rs576744119 | snp | A/T | | | | | GRCh38.p7 | 7:95465462 | AGAAGAGTTTAGAAG[A/T]CCAGAGGAATCATCC | 51666 |
rs576813667 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538540 | ACTCACTTTTAATGC[C/T]TATCTTTCAAAGTTG | 51666 |
rs576845571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95503301 | TGCATGAGGAGAAAG[C/T]AAGTGTTTTGCAGGT | 51666 |
rs576873344 | in-del | -/TTTAAA | | | | | GRCh38.p7 | 7:95462466 | CTCATATTTACTTCC[-/TTTAAA]TTTAAAAAAAAAATT | 51666 |
rs576898830 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASB4 | GRCh38.p7 | 7:95533439 | CTAGCTACAACTTTT[C/T]GTTTATCCTTTATTT | 51666 |
rs576903415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95524857 | AGTTCCTGCCGTTTG[C/T]AGTGGGGAGCAGCCT | 51666 |
rs576916359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95532035 | CTCAACAGACTGTGT[A/G]GGAGAGCTGGCCCCC | 51666 |
rs576925179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95494153 | GCATGTCTCTAGTGT[C/T]TTTCACTTAAATGAG | 51666 |
rs576963267 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472981 | CTCTCTCCACGCTCC[A/C]GCAGTTTGGCAGTAG | 51666 |
rs576965020 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95514590 | CCCTCCCTTTAAATT[C/T]ATCATTCTGACAGGC | 51666 |
rs576968123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95497054 | GGTAGGGTGGGAAGG[A/G]CAAGAGGGTAGAGGG | 51666 |
rs577004375 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95504977 | CACTTCAGGAAACAC[A/G]ACCTTAAGCAGTGCT | 51666 |
rs577035251 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95537998 | ATAGAACAGTAATAA[A/C]TAATATGTATAGTGT | 51666 |
rs577043882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95488144 | CAGGAGATAGAGACC[A/G]TCCTGCCTAACACGG | 51666 |
rs577106648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95494705 | CTATTGGCATTGACA[C/T]AGAAAGAAGGTTTAT | 51666 |
rs577133358 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95501040 | TTATTGATTTTTAAA[C/T]TTAATTAGTTTAAAC | 51666 |
rs577170696 | in-del | -/A/AAAAAAA/AAAAAAAA | | | intron-variant | ASB4 | GRCh38.p7 | 7:95530105 | GAGAAAAAGCAGGGC[-/A/AAAAAAA/AAAAAAAA]AAAAAAAAAAAAAAA | 51666 |
rs577362260 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASB4 | GRCh38.p7 | 7:95518705 | CAACAAGATGATGTA[C/G]AAATCTTTAACAGGG | 51666 |
rs577398154 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:95466768 | TCACAATCATGGCAG[A/G]AGACAAAGGAAGAAC | 51666 |
rs577425289 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95533889 | TCCTCTCTCGTGCCT[A/G]TTAGGATTTCTGAAG | 51666 |
rs577486915 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95467539 | CATTGTAAAATTGTG[C/T]GTGTGTGTGTGTGTG | 51666 |
rs577498960 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95511450 | AGTACGTGCACTTCT[C/T]GCAAGCATAGTTGAA | 51666 |
rs577582955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95512330 | ACCAAATGGGGCTAC[A/G]GATAATTCAAGTTGA | 51666 |
rs577613751 | in-del | -/T | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:95476098 | TTCTGGCACAGTAGA[-/T]TCTGGTCTGCCTTAT | 51666 |
rs577690493 | snp | C/G | 0.00318978 | 0.0398085 | | | GRCh38.p7 | 7:95461101 | AGGGAAATGTGGGGG[C/G]TGGAGACCCCTCACA | 51666 |
rs577725419 | snp | A/C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95478750 | AAATAGAGTTCCAAG[A/C/T]GAAGATGTGCTTGCG | 51666 |
rs577727395 | snp | A/G | 0.000399281 | 0.0141238 | nc-transcript-variant, intron-variant | LOC107986823 | GRCh38.p7 | 7:95471038 | GCCTGAAATGATTTA[A/G]TTGATGCCATATTGA | 51666 |
rs577741952 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95483128 | TCTAGTAGCCAGATA[A/G]GACCAAGTAAGTGAC | 51666 |
rs577749291 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469682 | AGAAAAGGAGTAAGT[C/T]ATATGGCTTATTATG | 51666 |
rs577754835 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95514917 | AATGCAAAGGGAGCT[A/G]GAGAAAAAACTTCCC | 51666 |
rs577786291 | in-del | -/AAT | 0.00119737 | 0.0244387 | intron-variant | ASB4 | GRCh38.p7 | 7:95493516 | TAAATAGCTTCTTTA[-/AAT]TAAATTATTTTTTCC | 51666 |
rs577878010 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95488268 | ATGGTGTGAACCCGG[A/G]AGGCGGAGCTTGCAG | 51666 |
rs577923458 | snp | C/T | | | | | GRCh38.p7 | 7:95479888 | ATCTGAATAGGATGG[C/T]TTCCTGGTGTCCCTT | 51666 |
rs577998209 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95476805 | AAAGAATCTGGAGAC[A/G]CATGGTATGAAACAT | 51666 |
rs578007579 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:95475954 | ATCACCTGAACTTTT[C/T]GGTCTCTATATATCA | 51666 |
rs578066433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95522012 | AAATATGGGTATGGT[A/G]TACAGGTGTCAATAT | 51666 |
rs578186908 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95498605 | ACTAGTCATTTATCA[C/G]ATACATAGTTTGCAC | 51666 |
rs578229474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASB4 | GRCh38.p7 | 7:95498032 | TTTTATTTCTCTTAT[A/G]TAAATACCTAGGAGT | 51666 |
rs745325998 | snp | C/G | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472686 | GGCTCAGGACAGGCT[C/G]TGAATTCCACAGCAG | 51666 |
rs745370005 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95517837 | TCAAGGAGTTCAAAC[A/G]AAAAGCAATAGAAAG | 51666 |
rs745412483 | in-del | -/A | | | intron-variant | ASB4 | GRCh38.p7 | 7:95529640 | AACTAATTCTTTTTT[-/A]AAAAAATTATATGTA | 51666 |
rs745417923 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95490788 | GGGCATATCTCTTTG[A/G]TTTCAGATTTAAATT | 51666 |
rs745425172 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95505135 | AGAAGAGAAAAATAC[A/G]TAATGTACGATGATT | 51666 |
rs745439193 | snp | A/G | | | | | GRCh38.p7 | 7:95479349 | CTCCTATAATGCTTC[A/G]CAATATGCAAAGTAC | 51666 |
rs745453915 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95530283 | CAGCCTGGGCAACAC[A/G]GTGAAACCCTGTCTC | 51666 |
rs745483587 | snp | A/G | 6.59533e-05 | 0.00574215 | missense | ASB4 | GRCh38.p7 | 7:95486122 | ACTGTTTTTGAAGTC[A/G]AAGATGAGAATATGG | 51666 |
rs745495163 | snp | A/C | 5.84004e-05 | 0.00540341 | intron-variant | ASB4 | GRCh38.p7 | 7:95536403 | GAACCATATATGTGC[A/C]TCAAACAGATGAAAC | 51666 |
rs745526597 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95506003 | GGCTCAAGCAGTCCT[C/T]CCACCTCAGCCTCCC | 51666 |
rs745536760 | in-del | -/C | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469994 | TATTCAACAGCACTT[-/C]CAGCTTATATAATTA | 51666 |
rs745538348 | in-del | -/CCCA | 1.6498e-05 | 0.00287206 | frameshift-variant | ASB4 | GRCh38.p7 | 7:95527942 | TGGACAGCGTGAATG[-/CCCA]CATGGAGACCCCCCT | 51666 |
rs745539840 | in-del | -/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95534467 | CTTCCAAGTTGTATT[-/C]TTTCTTCCTCCTATC | 51666 |
rs745539936 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95491843 | AAAGTGATGATTGTA[C/T]GCTGATGGCCCTTTT | 51666 |
rs745565907 | snp | A/G | 1.85506e-05 | 0.00304548 | intron-variant | ASB4 | GRCh38.p7 | 7:95495717 | AGAAAGCCTAGGTCA[A/G]GAAGTTAAACTTTCC | 51666 |
rs745594863 | snp | C/G | | | | | GRCh38.p7 | 7:95480151 | TTGTTCTGATCTATA[C/G]AAGGGTGGCTTATGG | 51666 |
rs745639050 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95525025 | GTCTGCGTGCCTAAA[C/T]TAACCTGGTCATGTG | 51666 |
rs745650838 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95511465 | CGCAAGCATAGTTGA[A/C]TTAACCTGGGTGGGG | 51666 |
rs745712354 | snp | C/T | | | | | GRCh38.p7 | 7:95468003 | GAGCCTGATTTGATC[C/T]AGCAAAAGAGATGGG | 51666 |
rs745790588 | snp | C/T | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469084 | TGGGCAGATTTAAAT[C/T]ATATAAGTTGTGTCT | 51666 |
rs745871085 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95531622 | GTTGAGCAGGAGAAT[G/T]GGTGCTCCTGGGCCT | 51666 |
rs745924253 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95532768 | GGGTTGGATGGTGAG[A/G]TGAGGTGTCTAAATC | 51666 |
rs745944956 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95500414 | TTTACTAAAGGAAAA[A/G]TAAATTAACCAGGCA | 51666 |
rs745986024 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95487623 | GGAGAGGTGGGGTTG[G/T]TTCTCCTACTTCCAC | 51666 |
rs746041552 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95524782 | ACAGCCAAGTATAAT[C/T]GGGTCCCCAGAGACC | 51666 |
rs746056768 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95488655 | TTATTAAATCAAAGG[A/G]GAAGTTTTGGACCTT | 51666 |
rs746088353 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95506826 | AAATGTTCCTGAATT[A/T]TTTCCTGGGTGAGTT | 51666 |
rs746097388 | snp | C/G | | | | | GRCh38.p7 | 7:95468395 | AACAGGAAAGGGCCA[C/G]TACTAATTCAGTAAA | 51666 |
rs746108479 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95521527 | TTGAAAATGTTCATA[C/T]ATTACTTCCCAGTAA | 51666 |
rs746118074 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95499234 | GTTGGCCTATAGATT[A/G]TATTTGAAGTCAAGG | 51666 |
rs746119065 | snp | A/C | 1.66651e-05 | 0.00288657 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95536532 | GTGGAGAAGAGCTAT[A/C]CCCGATGATGACTTG | 51666 |
rs746135243 | in-del | -/TC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515266 | CCTTCTTTCTTTCTT[-/TC]TCTTTCTTTCTTTCT | 51666 |
rs746173040 | snp | G/T | 1.64887e-05 | 0.00287125 | missense | ASB4 | GRCh38.p7 | 7:95528064 | AAAGCCGAAGTCAAT[G/T]CCCGAGATGACGACT | 51666 |
rs746182453 | snp | A/C | | | | | GRCh38.p7 | 7:95462344 | CTCCAGAGCAGCCCC[A/C]TTTGTAATAGCTTTT | 51666 |
rs746185282 | in-del | -/C | | | | | GRCh38.p7 | 7:95479772 | TTTGAGAGAATTGGA[-/C]CTTGGGTTCAAGAAG | 51666 |
rs746293351 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95495071 | GTGTATGTATTTGTC[G/T]TACTTTTGACATTTT | 51666 |
rs746305197 | snp | A/G | | | | | GRCh38.p7 | 7:95463298 | TCTGCTTCCCAAAGT[A/G]CTGGGATTACAGGCA | 51666 |
rs746340372 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95526853 | CCCCTAAGGGTCATT[C/T]GGTTCACCTCATTAA | 51666 |
rs746370299 | snp | C/T | 1.64953e-05 | 0.00287182 | missense | ASB4 | GRCh38.p7 | 7:95528031 | CACCACCTGGTCTGC[C/T]GCATGCTGCTTGACT | 51666 |
rs746399357 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95514446 | TGGTGAAATTTCTAT[C/T]AATTACATCATAAAA | 51666 |
rs746402276 | snp | C/T | | | | | GRCh38.p7 | 7:95482796 | GAGAGGATATATAGC[C/T]TGATCCAGGGGTCAG | 51666 |
rs746411715 | in-del | -/TAAAG | | | intron-variant | ASB4 | GRCh38.p7 | 7:95502085 | CAGAAGTTTTTCAAT[-/TAAAG]TAATGAGGCTAACAA | 51666 |
rs746441233 | in-del | -/TT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95495740 | AACTTTCCTTTTCCT[-/TT]TTTTTTTTTTTTTCA | 51666 |
rs746454174 | snp | A/C | | | | | GRCh38.p7 | 7:95460730 | CTGCAGAAAGTTGCA[A/C]AAGTAATGAGGAGCC | 51666 |
rs746459820 | in-del | -/CTTA | | | intron-variant | ASB4 | GRCh38.p7 | 7:95535093 | ACACATGCGCACACT[-/CTTA]CTTAGTTGGATATTA | 51666 |
rs746476613 | snp | C/G | | | missense | ASB4 | GRCh38.p7 | 7:95528245 | CCCAGCCTGAGATCT[C/G]CTACCAGCTCCTGTT | 51666 |
rs746500928 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95491945 | AATCCCTAGCCCCAC[A/G]TTACCACCAAAGTTT | 51666 |
rs746520954 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95506532 | CCCCCGACTTAGAGT[A/G]GAATTCTAGATTCAT | 51666 |
rs746550092 | snp | C/T | | | | | GRCh38.p7 | 7:95480212 | TACTTTTCTTGGTAG[C/T]ACATATTACCATGTG | 51666 |
rs746582005 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95493542 | TTTTTCCCCTCTGGA[A/C]AGAGAGACAATAGCT | 51666 |
rs746595931 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95529905 | CACACAGAGTAAGTG[C/T]CAAGTTCACTCATTT | 51666 |
rs746622505 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95525211 | CTGGAAGAAACCAAC[C/G]CTAGACACTTTAATT | 51666 |
rs746653242 | snp | A/G | | | | | GRCh38.p7 | 7:95460786 | GAAAATGTCTCCAGG[A/G]TATGTCAGAGACCTT | 51666 |
rs746653735 | snp | A/C | 4.94743e-05 | 0.0049734 | missense | ASB4 | GRCh38.p7 | 7:95495837 | GTTTGGCCATGTGGA[A/C]TGTCTTCTGGTGCTA | 51666 |
rs746677778 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95512872 | ACGACCCTCCAAAGA[C/T]GTCTAAGTCCTCATC | 51666 |
rs746708308 | snp | G/T | | | | | GRCh38.p7 | 7:95481290 | CAGTTCCAGTTGCTG[G/T]TGTTACTTACAAACA | 51666 |
rs746737726 | snp | C/T | 5.9288e-05 | 0.00544431 | intron-variant | ASB4 | GRCh38.p7 | 7:95495737 | TTAAACTTTCCTTTT[C/T]CTTTTTTTTTTTTTT | 51666 |
rs746742911 | snp | A/G | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469382 | ATTCAATAACAATTT[A/G]TTGAATGAAAGAATA | 51666 |
rs746873159 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95533049 | TCCCTAACCTTCTCA[C/G]TTCACTTAACAGATT | 51666 |
rs746949175 | in-del | -/TG | | | | | GRCh38.p7 | 7:95479076 | CAATGTCCAGGACAC[-/TG]TGTTCCATAAGGGAG | 51666 |
rs746970337 | snp | C/G | 1.75105e-05 | 0.00295888 | intron-variant | ASB4 | GRCh38.p7 | 7:95536429 | GAAACTCTGTGCTTC[C/G]TCTGCAGGTGATACA | 51666 |
rs747018691 | snp | A/T | 0.00010628 | 0.00728895 | intron-variant | ASB4 | GRCh38.p7 | 7:95527763 | AATGAACCTTAGGAA[A/T]AATGACAAAACATGT | 51666 |
rs747027560 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95488976 | ATTCAACATTTGATA[A/G]TCCTATAGAAAGTGA | 51666 |
rs747150015 | snp | C/T | | | | | GRCh38.p7 | 7:95477030 | GAAAGATATGGTTTA[C/T]GTGGATTAAAACAAA | 51666 |
rs747168525 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95520259 | AGTTACGGACAAAGG[A/G]AGCAGAAACAAAATA | 51666 |
rs747179240 | snp | C/T | | | | | GRCh38.p7 | 7:95466251 | GTCAAAGCCACACAG[C/T]TCTAAGAGGTGAGGT | 51666 |
rs747194594 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95508074 | TTATTTTTTTTTTAG[A/G]TTTTAGATGATAGAA | 51666 |
rs747210437 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95495116 | TTTATTTTGCCCTTA[C/T]TTTCTAAATCGTTTA | 51666 |
rs747216323 | snp | A/C | 1.64874e-05 | 0.00287113 | missense, intron-variant | ASB4 | GRCh38.p7 | 7:95537650 | ACTTATCGAGATGTG[A/C]CATTAGAAGAACATT | 51666 |
rs747249554 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95509345 | TACCACAGGCCAGAG[A/T]TAAGCATCCCACATC | 51666 |
rs747252251 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95522313 | CATTCATGATGGCAA[G/T]GATGCTCGTGGTGTT | 51666 |
rs747253499 | snp | C/T | 4.94597e-05 | 0.00497266 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95495978 | AAAGCTCAATTGCTA[C/T]TCCTTAAGTGGACAC | 51666 |
rs747277384 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95493473 | AGTTCATTCATTCCT[G/T]TGGGATTAATCACTG | 51666 |
rs747301513 | snp | A/G | | | downstream-variant-500B, intron-variant | ASB4 | GRCh38.p7 | 7:95540579 | ACCCTGGGCAAAGCA[A/G]CAGAGGAAATTACAT | 51666 |
rs747338564 | snp | C/G | 1.69344e-05 | 0.00290979 | missense | ASB4 | GRCh38.p7 | 7:95485979 | GAGGAAGGATGGACG[C/G]CACCACTGCCCCTGT | 51666 |
rs747350836 | snp | C/G | | | | | GRCh38.p7 | 7:95466329 | CCCTTTAACATGATA[C/G]AATGTTTATAGTGCG | 51666 |
rs747395810 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95496203 | AAAAAATACATAGTT[C/G]TGTTGATTCAGGTAA | 51666 |
rs747442580 | in-del | -/TTTCTCTT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515158 | GTTTTTCTTTCTTTC[-/TTTCTCTT]TCTCTTTCTTTCTTT | 51666 |
rs747451430 | snp | A/C | 3.29739e-05 | 0.00406028 | missense | ASB4 | GRCh38.p7 | 7:95528084 | AGATGACGACTTTAA[A/C]TCTCCCCTCCACAAG | 51666 |
rs747451691 | snp | A/C | | | | | GRCh38.p7 | 7:95468064 | AAACATCACATTTGC[A/C]TTGATTATAGAGCCT | 51666 |
rs747489765 | in-del | -/CC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515311 | CTTTCTTTCTTTCTT[-/CC]TCTTTCTTCCTTCCT | 51666 |
rs747492561 | in-del | -/TT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515290 | TTCTTTCTTTCTTTC[-/TT]TCTTTCTTTCTTTCT | 51666 |
rs747502429 | snp | C/T | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484713 | TCCACAAACGACATA[C/T]AAAAATGCAATTTAT | 51666 |
rs747511915 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515496 | TCTCTGCTCACTGCA[A/T]CCTCTGCATCCCGTG | 51666 |
rs747581279 | snp | C/T | 1.64944e-05 | 0.00287175 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95528198 | TGCTGCCATCCAGTA[C/T]GTGCTGAAGGTCACC | 51666 |
rs747628738 | snp | A/C | | | | | GRCh38.p7 | 7:95464316 | TTACATTATTTGAAC[A/C]TAAATACATTTATAT | 51666 |
rs747670065 | snp | G/T | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469445 | TGTGTCAGGTAATGA[G/T]CTGTCTCCTACAAGT | 51666 |
rs747760004 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513979 | AAAATCACCCTCACA[A/G]CTCCTGGACCTCCAC | 51666 |
rs747811468 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95514794 | AAATGGCCTTTCTGC[A/T]AGAAACAGACAAAAA | 51666 |
rs747827455 | snp | C/T | 1.64866e-05 | 0.00287106 | missense | ASB4 | GRCh38.p7 | 7:95528104 | CCCTCCACAAGGCAG[C/T]CTGGAACTGTGACCA | 51666 |
rs748032533 | in-del | -/TA | | | intron-variant | ASB4 | GRCh38.p7 | 7:95527192 | GTGTGTGTGCATGTG[-/TA]TGTGTGTGTGTGCAT | 51666 |
rs748069035 | snp | G/T | 1.77609e-05 | 0.00297995 | intron-variant | ASB4 | GRCh38.p7 | 7:95537522 | TGATTTTTATTGATG[G/T]AAACTGTGGGGCCTT | 51666 |
rs748097345 | snp | A/T | 1.65872e-05 | 0.00287981 | stop-gained | ASB4 | GRCh38.p7 | 7:95536524 | AACACAAAGTGGAGA[A/T]GAGCTATCCCCGATG | 51666 |
rs748113428 | snp | C/T | | | | | GRCh38.p7 | 7:95477143 | CTGCAGCTGTTCTTC[C/T]GGGTTCATTTATCGA | 51666 |
rs748145464 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95490190 | GGCAGGTACTCTGTT[G/T]CCTTTACTAAGTAGC | 51666 |
rs748149300 | snp | A/G | 0.000148413 | 0.00861305 | missense | ASB4 | GRCh38.p7 | 7:95495860 | TGGTGCTACTGGACC[A/G]CAATGCTACAATCAA | 51666 |
rs748220169 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95511207 | ACAGAATAACGGTGG[A/T]CCCCTCTCTTTTCCA | 51666 |
rs748244377 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95519773 | TGATGTTAAAAAGGC[A/G]GCCATTAGTGATTTA | 51666 |
rs748348441 | snp | A/G | 1.68661e-05 | 0.00290392 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95537768 | TTATTAAGCCTTATG[A/G]GACAGCAGTTCCCAA | 51666 |
rs748385542 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95529908 | ACAGAGTAAGTGTCA[A/G]GTTCACTCATTTGTT | 51666 |
rs748404594 | snp | C/T | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95483744 | TCTGTGTTTGTTCAC[C/T]GCTGTATCTGCAGTG | 51666 |
rs748489210 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95516896 | TTCTGTGACTTCAAA[G/T]GTCATCAAATGGTGT | 51666 |
rs748523442 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95531383 | CTGCATATTGTCGTT[A/C]AAAGACTACTTTCCC | 51666 |
rs748547154 | snp | A/G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95492671 | CTGGGATCATTTTTC[A/G/T]TCCCATTGCAGAAGC | 51666 |
rs748580432 | snp | C/T | | | | | GRCh38.p7 | 7:95467386 | ACTTTTTGTGAAAGC[C/T]CAGTAGTGGATGGGT | 51666 |
rs748598653 | in-del | -/C | 1.81122e-05 | 0.00300928 | intron-variant, frameshift-variant | ASB4 | GRCh38.p7 | 7:95528367 | CCTTGTCTGAAATCT[-/C]CCAAGTAACTCAAGC | 51666 |
rs748605208 | snp | C/T | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472740 | TGCAGTATGATAAAA[C/T]GCGGTTAACCTCAGC | 51666 |
rs748611858 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95517974 | AGATAAATTACTTGT[G/T]GAGCAATGTTCTACT | 51666 |
rs748655880 | snp | C/T | 1.67181e-05 | 0.00289115 | missense | ASB4 | GRCh38.p7 | 7:95485990 | GACGGCACCACTGCC[C/T]CTGTCACTAAATCTG | 51666 |
rs748671033 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95505209 | TGTCTACATGGAAAA[C/T]CCAAGAAAATCTACA | 51666 |
rs748709125 | snp | C/T | 3.29549e-05 | 0.00405911 | missense | ASB4 | GRCh38.p7 | 7:95486096 | TGATCCAAAGGCAAA[C/T]AGATGTGGACACTGT | 51666 |
rs748736410 | snp | G/T | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95483584 | TCAAATGATTAGATA[G/T]AAACAAACTATATTA | 51666 |
rs748737287 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515367 | TTTCTTTCTTTCTTT[C/T]CTTTCTTTCTTTTCT | 51666 |
rs748752076 | snp | C/T | 6.59294e-05 | 0.00574111 | missense | ASB4 | GRCh38.p7 | 7:95486111 | TAGATGTGGACACTG[C/T]TTTTGAAGTCGAAGA | 51666 |
rs748825244 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95534337 | TAAAAACGTAAAACT[C/G]CATTAAAAAAAAAAA | 51666 |
rs748838993 | snp | A/G | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484246 | CTGAGGTGGGAGGAT[A/G]GCTTGAGCCTGAGAG | 51666 |
rs748911012 | in-del | -/AA | | | intron-variant | ASB4 | GRCh38.p7 | 7:95521687 | TCAGCAGTTGAAATT[-/AA]AAAAAAAAAAACAGT | 51666 |
rs748970495 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95503781 | GCAACTGAAAACCGA[C/T]GTAATTTCATTTGCT | 51666 |
rs749023996 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95490474 | TGTGCTTCAGTCTGT[A/C]ATCCTTCAGGACTGT | 51666 |
rs749061751 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95536428 | TGAAACTCTGTGCTT[C/T]CTCTGCAGGTGATAC | 51666 |
rs749072648 | in-del | -/ACCACTC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95524991 | CAAATAAATTCTGTA[-/ACCACTC]ACCCTTCAAAGTGTC | 51666 |
rs749091769 | snp | C/T | | | | | GRCh38.p7 | 7:95478872 | AGTATGTAATTACAA[C/T]TGAGAATGAATACGC | 51666 |
rs749185566 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95524113 | TGCATACCCAGTGAC[C/G]CAGCAATTCCACTCA | 51666 |
rs749211498 | snp | C/T | 3.43247e-05 | 0.00414261 | intron-variant | ASB4 | GRCh38.p7 | 7:95496085 | GGGTGGCCAACATTG[C/T]TGTCTGCTTGTACAC | 51666 |
rs749258058 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95511297 | CAGGGAAGGCCCAGT[G/T]AGGGAGTCCCCTGAA | 51666 |
rs749337442 | snp | C/G | | | | | GRCh38.p7 | 7:95467841 | CATCTCAAGAGGCTT[C/G]ACCACATTCTTGGAG | 51666 |
rs749368675 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95512721 | AATGCTGGCTTAGAA[G/T]AATGAAATTAGGGCC | 51666 |
rs749392421 | snp | C/T | | | downstream-variant-500B, intron-variant | ASB4 | GRCh38.p7 | 7:95540481 | TAGTAGTAAAGAAAT[C/T]GTACTGAATCATTCT | 51666 |
rs749396510 | snp | A/G | 3.42642e-05 | 0.00413895 | splice-acceptor-variant | ASB4 | GRCh38.p7 | 7:95536436 | TGTGCTTCCTCTGCA[A/G]GTGATACAGGCCTGC | 51666 |
rs749427514 | snp | A/G | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95485293 | AAAAAACAGGATTCA[A/G]TAAAGTTCATTCACA | 51666 |
rs749441976 | in-del | -/AC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95499553 | AATAGTTTTGGTGAA[-/AC]AGTGTTAAAAGCCAG | 51666 |
rs749472207 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95518353 | TCTCCCCATGATATT[A/G]TGATAGTGGGGCAAG | 51666 |
rs749526843 | snp | A/T | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473444 | AGAGCCACAGGTTTA[A/T]CCAGGACAATAACAA | 51666 |
rs749548066 | in-del | -/A | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513341 | TGTGTGTTCAGAGAC[-/A]GGGAATGGAATGATT | 51666 |
rs749548166 | snp | A/C | | | missense | ASB4 | GRCh38.p7 | 7:95486042 | GAAATTTCCTTGAGG[A/C]GCTAAAGTCCAATGA | 51666 |
rs749591453 | snp | C/T | 3.29989e-05 | 0.00406182 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95527907 | GCTGGTGGCCTTCTA[C/T]GTGGAACACGGGGCC | 51666 |
rs749592380 | in-del | -/TC | 1.64953e-05 | 0.00287182 | frameshift-variant | ASB4 | GRCh38.p7 | 7:95527995 | CCCTCCGCTTTAAGG[-/TC]AGCAGGAGTACAGCA | 51666 |
rs749605504 | snp | C/T | | | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95474108 | TTACTTGATCTGGCC[C/T]AGACTATAGATCACA | 51666 |
rs749644546 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95505503 | TTATTCCTTCTTCAG[A/G]GGCAACCACTTTTAC | 51666 |
rs749689564 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95506766 | TATCTTCATCCTTTG[C/T]ACTGAGTCCATTCAA | 51666 |
rs749714567 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95492440 | CTTCCACAAAGACAA[A/T]GACAGATGAAAACTG | 51666 |
rs749733151 | snp | C/T | | | | | GRCh38.p7 | 7:95475406 | AATTATTTTTTGAGA[C/T]GGAGACTGGCTTTGT | 51666 |
rs749816243 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95493688 | TTCTGTCCTGATCCC[C/T]CAACCCCCCAGTTCT | 51666 |
rs749830093 | in-del | -/A | 1.64959e-05 | 0.00287188 | frameshift-variant | ASB4 | GRCh38.p7 | 7:95486131 | GAAGTCGAAGATGAG[-/A]ATATGGTTTTGGCAT | 51666 |
rs749844932 | snp | C/T | 1.64928e-05 | 0.00287161 | missense | ASB4 | GRCh38.p7 | 7:95495812 | CCACAGGCCTCCATC[C/T]CTCTGTCTTGTTTGG | 51666 |
rs749893678 | in-del | -/CA | | | intron-variant | ASB4 | GRCh38.p7 | 7:95510281 | ATTGGAGTTGCAAAG[-/CA]CACTCTCAACACAGA | 51666 |
rs749894902 | snp | A/T | | | upstream-variant-2KB, utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485741 | TTCATATTGACACTA[A/T]ATATTACTGAATGGA | 51666 |
rs749939144 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95519206 | GAAAAAAGCAACCAA[C/T]TGAAAATATGCTTTG | 51666 |
rs749973401 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95534258 | TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 51666 |
rs750015924 | snp | A/G | | | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95473789 | GGGGAACAATGGTCA[A/G]GGACTCCAGGCCTGA | 51666 |
rs750022948 | snp | C/G | | | downstream-variant-500B | LOC107986823 | GRCh38.p7 | 7:95474665 | TAGCTGAAACTACGG[C/G]CACATGCCACCATGC | 51666 |
rs750090665 | snp | A/C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95494791 | AAAAGACCAGCTCAG[A/C/T]GTATAGAAGTCAGAG | 51666 |
rs750176602 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95493060 | GCTCCCCAGCCCAGA[A/C]TGTCTATGACACTAC | 51666 |
rs750196945 | snp | G/T | 1.6495e-05 | 0.0028718 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95528024 | CACGGAGCACCACCT[G/T]GTCTGCCGCATGCTG | 51666 |
rs750221999 | snp | A/C | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538632 | GTAAAGTAGAGGGAT[A/C]TCCTGCTCTTGTTAG | 51666 |
rs750273721 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95512137 | GTAGCCTATTAGACC[A/G]GGGGTGGTGTTCAAC | 51666 |
rs750284203 | snp | C/T | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539604 | GGATGGAGCTGGAGG[C/T]CATTATTCTAAGTGA | 51666 |
rs750285430 | in-del | -/T | 3.34102e-05 | 0.00408705 | frameshift-variant | ASB4 | GRCh38.p7 | 7:95485992 | CGGCACCACTGCCCC[-/T]GTCACTAAATCTGGA | 51666 |
rs750337784 | in-del | -/A | | | intron-variant | ASB4 | GRCh38.p7 | 7:95495441 | AAAATACAATTACAT[-/A]AATGAAGATCCCAAA | 51666 |
rs750339193 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95527182 | AAAGTCGTGTGTGTG[C/T]GTGCATGTGTATGTG | 51666 |
rs750370829 | snp | A/T | 4.95479e-05 | 0.0049771 | missense | ASB4 | GRCh38.p7 | 7:95527866 | GAGACGCCCTTGCAC[A/T]CGGCTGCCCACTTCG | 51666 |
rs750422836 | snp | C/T | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95470201 | TTGTTCCAGTTTTCT[C/T]ATAAGTGTAATGTGA | 51666 |
rs750427927 | snp | C/G/T | 4.94966e-05 | 0.00497456 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95527955 | TGCCCACATGGAGAC[C/G/T]CCCCTGGCCATCGCC | 51666 |
rs750452233 | snp | C/G | 1.6477e-05 | 0.00287024 | missense | ASB4 | GRCh38.p7 | 7:95486074 | TTCGGAAAATTGAAG[C/G]CTATTTTGATCCAAA | 51666 |
rs750487751 | in-del | -/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95523436 | CAATTAACTAAAAAA[-/T]GAAATACCATTAGTT | 51666 |
rs750547646 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95501148 | AACATTTTTTGTCTC[A/G]CTTTTCGTAATAATG | 51666 |
rs750551677 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95501911 | ATCCACTTACTCTTT[C/T]AAGCCATGTCATCAA | 51666 |
rs750558529 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95529072 | ACTAAGACATGGGAC[A/G]TATCCTCAAGAAGCT | 51666 |
rs750589877 | in-del | -/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515612 | ATAGAGACGGGGTTT[-/C]CCCATGTTGACCAGG | 51666 |
rs750596265 | snp | A/G/T | 3.29882e-05 | 0.00406118 | missense | ASB4 | GRCh38.p7 | 7:95528178 | CTCATGGATATCAAC[A/G/T]GCTGTGCTGCCATCC | 51666 |
rs750599766 | in-del | -/TC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515220 | CTTTCTTTCTTTCTT[-/TC]TTTCTTTCTTTTTCT | 51666 |
rs750675982 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95503241 | ATATAAATAAGAAAA[C/T]AAACCTGTGAATCAG | 51666 |
rs750679959 | snp | A/G | 1.72311e-05 | 0.00293518 | utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485968 | TTCCAGAGGGAGAGG[A/G]AGGATGGACGGCACC | 51666 |
rs750695451 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95489754 | ATGCAATAAGTCATT[A/G]AAAGTCAAGGGATGT | 51666 |
rs750696626 | snp | A/G | 0.000115492 | 0.00759819 | missense | ASB4 | GRCh38.p7 | 7:95528251 | CTGAGATCTGCTACC[A/G]GCTCCTGTTGAACCA | 51666 |
rs750745953 | snp | C/T | | | | | GRCh38.p7 | 7:95476706 | GGAATATTTTCAGCC[C/T]AGGAGAAAAATTGTG | 51666 |
rs750751121 | in-del | -/C | | | downstream-variant-500B, intron-variant | ASB4 | GRCh38.p7 | 7:95540665 | TCTTGAAGAAAAAAA[-/C]AATCTCTCTTCTGAA | 51666 |
rs750802109 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95535809 | GTTTAGTACATGACA[A/C]CAGCCCTCTGCAGGC | 51666 |
rs750853468 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95516813 | TGTTTAAATATTTGC[A/G]TGTCCTAGGGCTCAG | 51666 |
rs750902852 | snp | C/G | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472982 | TCTCTCCACGCTCCA[C/G]CAGTTTGGCAGTAGA | 51666 |
rs750962643 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95510634 | AATTTTCTCAAGTTT[A/G]GGTTGCTTACTGCAG | 51666 |
rs750981214 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95497981 | TTTCAAAGAAAGGCT[C/G]ATATAAACATTTGCA | 51666 |
rs751022766 | snp | A/G | 3.29859e-05 | 0.00406102 | missense | ASB4 | GRCh38.p7 | 7:95496015 | TTGCACTTTTGTACA[A/G]CTCCAAGTTCCATTC | 51666 |
rs751027035 | snp | C/T | | | | | GRCh38.p7 | 7:95463754 | CCTAGTCTCAGGTAT[C/T]TCTTTATAGCAGTGT | 51666 |
rs751030770 | snp | G/T | | | | | GRCh38.p7 | 7:95475284 | CCATCTTTCCTTACA[G/T]AGTCCCTCCCCACGC | 51666 |
rs751083682 | snp | A/G | | | | | GRCh38.p7 | 7:95461692 | TTGGGAGGGACCAGG[A/G]TGGAATGATATGGTT | 51666 |
rs751123866 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95507480 | AATCAATTAGGTCCC[A/G]ATGCTATGTTCTGTA | 51666 |
rs751212546 | snp | C/T | 1.84858e-05 | 0.00304016 | intron-variant | ASB4 | GRCh38.p7 | 7:95536584 | TCTAATAGTTTTCAC[C/T]ATCAAGTACTTCCAG | 51666 |
rs751224870 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95491639 | AGCATGCTGTGGTCA[A/T]TGGTGGTTATATTTT | 51666 |
rs751238773 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95508811 | GAGAAGAAAGGAACA[C/T]TTAATGGACAAAGAG | 51666 |
rs751240299 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95519056 | CCCCAGACTCTAGAG[A/C]ATGTGAGTGTTAGAT | 51666 |
rs751253040 | snp | A/T | 1.64933e-05 | 0.00287165 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95495939 | CAATGTGGATTGTGT[A/T]AAGATCCTCTGTGAT | 51666 |
rs751256126 | snp | A/G | | | | | GRCh38.p7 | 7:95482275 | TTAGATACAGTATTT[A/G]TTTATATAGCTATGG | 51666 |
rs751308441 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95495252 | TTTTTTAAAAAGATT[A/G]AATATATTCATATGT | 51666 |
rs751330878 | snp | C/T | 3.79954e-05 | 0.00435847 | utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485932 | GCTCGGTGCTGTTCT[C/T]TCGATAAATCACAAC | 51666 |
rs751383094 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95527364 | ATCTGCTATGAAAGA[A/G]AAGAAAAGTATTATT | 51666 |
rs751394838 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95532333 | AGCCAATGTGTAAAT[C/T]ACATAAGCGGGGGAA | 51666 |
rs751408666 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95514567 | TGGCTTCAGGGTACA[A/C]AAATTCTCCCTCCCT | 51666 |
rs751425272 | in-del | -/A | | | intron-variant | ASB4 | GRCh38.p7 | 7:95511749 | GTCTATGCTTTCACT[-/A]ATCCTCACAACTATC | 51666 |
rs751508144 | in-del | -/AGA | 3.29709e-05 | 0.0040601 | cds-indel, intron-variant | ASB4 | GRCh38.p7 | 7:95537655 | TCGAGATGTGCCATT[-/AGA]AGAACATTACACAAC | 51666 |
rs751531667 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95503366 | CATCTTGTTTTCTTT[C/G]CTTTGCATTTTTATG | 51666 |
rs751560738 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95523438 | AATTAACTAAAAAAG[A/T]AATACCATTAGTTAA | 51666 |
rs751589246 | in-del | -/ATTTGGGG | | | intron-variant | ASB4 | GRCh38.p7 | 7:95517396 | ATATATGATGATAGA[-/ATTTGGGG]ACCTGTCTGTTCACA | 51666 |
rs751647487 | snp | A/C | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472345 | TGATCTGTTGCCGCC[A/C]TCTTGAAAATCTCAA | 51666 |
rs751699028 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95489913 | GACGAAGGACTGTCC[A/G]TAAAACTGTTTCCAA | 51666 |
rs751723769 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95504269 | GTTCCTTAGCAGAAA[A/G]TGACATGGGGGCAAT | 51666 |
rs751728394 | snp | A/T | 3.29533e-05 | 0.00405901 | missense | ASB4 | GRCh38.p7 | 7:95486078 | GAAAATTGAAGGCTA[A/T]TTTGATCCAAAGGCA | 51666 |
rs751752060 | snp | A/T | | | | | GRCh38.p7 | 7:95478400 | CTCTGTGGGGCAGGG[A/T]TGTTTGATCTGAAAA | 51666 |
rs751764899 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95535972 | AGTTTCCCAGGCAGC[C/T]GGGAATGTATTCTGT | 51666 |
rs751814217 | snp | C/G | 3.30169e-05 | 0.00406293 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95528270 | CCTGTTGAACCATGG[C/G]GCTGCCCGAATATAC | 51666 |
rs751816270 | snp | A/G | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472857 | TGCACTTCCCATCCC[A/G]CGGTGTTTGCATAAT | 51666 |
rs751858651 | snp | C/T | 1.67545e-05 | 0.0028943 | intron-variant | ASB4 | GRCh38.p7 | 7:95486170 | CAAGGTAAAAACATA[C/T]AGGTGTTATTGTAGA | 51666 |
rs751861926 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95524648 | TGAATTTATTTGGAA[A/T]TAAGGTTGCTGCAGA | 51666 |
rs751874210 | snp | A/G | | | | | GRCh38.p7 | 7:95467470 | TTTCTTACTATTGGC[A/G]TCAGGGAGTGGGATA | 51666 |
rs751937715 | in-del | -/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95536859 | TTGGAATTGCTTATA[-/T]TAGCATTTTTACCAG | 51666 |
rs751969861 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95510950 | TTATTATCCTCTGAA[C/T]ATTTTAAATACCCAT | 51666 |
rs752063174 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95500745 | TCTGAAAGACTGGAA[C/T]CTTTCAGTTATCCTG | 51666 |
rs752093240 | snp | A/C | | | | | GRCh38.p7 | 7:95468627 | CATATCTGTCATTTT[A/C]AGTGCTCATTACAAT | 51666 |
rs752132995 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95509083 | TGGGTCATTCATGTG[G/T]TATTAAAGACCCCCA | 51666 |
rs752197343 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95518677 | AACTGGAACCACTAA[C/G]TCAAACTGAGTCCAA | 51666 |
rs752256411 | snp | A/T | | | | | GRCh38.p7 | 7:95483370 | TATTGTTCCTCCATG[A/T]ATCCCATATTCCCTG | 51666 |
rs752274771 | snp | A/G | 1.65809e-05 | 0.00287926 | synonymous-codon, intron-variant | ASB4 | GRCh38.p7 | 7:95537735 | AAAGTACTTGCTTTT[A/G]GAGCCAGAGGGAATT | 51666 |
rs752279234 | in-del | -/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95496377 | CTCAAAGAAAGTATA[-/T]TCTAATAAGGGAGAC | 51666 |
rs752314843 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95496828 | ACTCCAGCCTGACTG[A/G]CAGAGTGAGACCCTG | 51666 |
rs752335875 | snp | C/T | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539984 | GGCGTATTCTAGCAG[C/T]AAAGCTTGTGATGCA | 51666 |
rs752383074 | snp | G/T | | | intron-variant, nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471711 | ATTAGGACTTTAGAG[G/T]ACAGCAGTGGTGGCA | 51666 |
rs752392005 | snp | G/T | 3.33289e-05 | 0.00408207 | missense | ASB4 | GRCh38.p7 | 7:95496047 | CTGTGCCAAGCAATT[G/T]GTTTGGAGAGGTAAG | 51666 |
rs752476807 | in-del | -/TT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515209 | TTCTTTCTTTCTTTC[-/TT]TTTCTTTCTTTCTTT | 51666 |
rs752482006 | snp | G/T | 1.64939e-05 | 0.0028717 | missense, intron-variant | ASB4 | GRCh38.p7 | 7:95537637 | AGGACTCTCATGCAC[G/T]TATCGAGATGTGCCA | 51666 |
rs752536989 | snp | G/T | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472499 | AAACAAGGTTCTATC[G/T]CCCTGTGATTCCTGT | 51666 |
rs752539959 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95530634 | CTGAAGTGGAGTGAG[C/T]AAGGGGAAGATAAAT | 51666 |
rs752571067 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95491371 | TTAGAGGGAGGCAGC[A/C]GCTGCTTCACCTCCC | 51666 |
rs752571238 | snp | A/G | 3.78379e-05 | 0.00434943 | utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485935 | CGGTGCTGTTCTCTC[A/G]ATAAATCACAACAAA | 51666 |
rs752580783 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95504488 | GCGTTCCATCTTTTC[A/G]TCTTCTGCGTTATAC | 51666 |
rs752600735 | snp | A/C | | | | | GRCh38.p7 | 7:95462096 | GACTAATATAGTGGC[A/C]TTCTCTAGCACCCAG | 51666 |
rs752605802 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95504522 | GTAATAGCATAAATC[A/T]GACCATGTTAGACAT | 51666 |
rs752612166 | snp | A/G | | | | | GRCh38.p7 | 7:95460100 | CCCCAGCCATGTGGA[A/G]TTGTAGGTCAATTGA | 51666 |
rs752633778 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95536181 | AGACTTCTGAAAATC[A/G]TTTTAGCATTCCAGG | 51666 |
rs752644523 | in-del | -/TT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515219 | CTTTCTTTCTTTCTT[-/TT]TCTTTCTTTCTTTTT | 51666 |
rs752702027 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95524002 | AATACCAATGTTGAT[A/G]AGGATGTAATACAAT | 51666 |
rs752705635 | in-del | -/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95529737 | AGAATAAGAATAATG[-/T]TACAGTAACTGTCCT | 51666 |
rs752758293 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95537466 | ACCAATAGAGACCCT[A/G]GGAAGCTGCCATTAC | 51666 |
rs752765744 | snp | A/G | 1.6498e-05 | 0.00287206 | missense | ASB4 | GRCh38.p7 | 7:95527962 | ATGGAGACCCCCCTG[A/G]CCATCGCCGCCTACT | 51666 |
rs752953066 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95507841 | TGTTAAATACTACGG[A/T]GAGATCCAGTAAGTT | 51666 |
rs752971079 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95511489 | GGTGGGGGCAGGAGG[A/C]AGAGCCGTGAAGAAA | 51666 |
rs752990638 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95512528 | GGAAAAATAAGTCCT[C/G]GAAAATCCATGTTAA | 51666 |
rs753040818 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95499328 | CAATGAATTCTAACA[C/T]TTCAATGTTAGAAGG | 51666 |
rs753065529 | snp | A/G/T | 3.41724e-05 | 0.00413343 | intron-variant | ASB4 | GRCh38.p7 | 7:95486199 | GAACTGTTAGAAAAT[A/G/T]ATTTAAAAAAATGCA | 51666 |
rs753118507 | snp | A/G | 1.65124e-05 | 0.00287331 | missense | ASB4 | GRCh38.p7 | 7:95495785 | CTAGCTATAAATTGA[A/G]GTCTTCCTGGGCCAC | 51666 |
rs753167667 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95500076 | CAGAATATTTATAGA[C/T]TTGATGGTGCTACGA | 51666 |
rs753190984 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95521880 | TTTTAGAACAGTAGT[C/T]ACCTCTGTGGAGGAA | 51666 |
rs753204860 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95536089 | CACTTGCTCGTGGAA[A/G]GTGAAAGAAATTGGT | 51666 |
rs753213929 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95519338 | GAATAGAATAAAAGG[A/G]ATCTAACCTTTGAAT | 51666 |
rs753216940 | snp | C/T | 2.54378e-05 | 0.00356627 | intron-variant, utr-variant-3-prime | ASB4 | GRCh38.p7 | 7:95528422 | TAACTACCTCTGATC[C/T]TCTTTGACCTTCCAT | 51666 |
rs753220748 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95486981 | GAGCATACTGCAAAC[A/T]TGCTGCTCAACATCA | 51666 |
rs753245430 | snp | A/G | 4.95855e-05 | 0.00497899 | missense | ASB4 | GRCh38.p7 | 7:95528293 | GAATATACCCTCCAC[A/G]GTTCCATAAGGTGAG | 51666 |
rs753258514 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95533681 | TAAATCCTGACTCTA[C/T]CATTTCCTAGCTAAA | 51666 |
rs753298617 | snp | A/C | 6.70443e-05 | 0.00578945 | intron-variant, utr-variant-3-prime | ASB4 | GRCh38.p7 | 7:95528409 | TTGAGTCCTGGGCTA[A/C]CTACCTCTGATCCTC | 51666 |
rs753323979 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95496950 | TAGCTATAGGAAATA[C/G]CTTGAGCAAAATTGC | 51666 |
rs753329616 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95531053 | ATGCCTTGGCAATGC[A/G]ATGCAGACTCAGTCC | 51666 |
rs753349775 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95498959 | CAATTGGCAATATAT[A/G]TATGGGTTTATTTCT | 51666 |
rs753406766 | snp | A/G | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484521 | ACAAGCTGTATACCT[A/G]TAACTTGCCAATTTC | 51666 |
rs753535152 | snp | A/C/G/T | 0.00031344 | 0.0125152 | missense | ASB4 | GRCh38.p7 | 7:95527954 | ATGCCCACATGGAGA[A/C/G/T]CCCCCTGGCCATCGC | 51666 |
rs753554353 | snp | A/G | | | stop-gained | ASB4 | GRCh38.p7 | 7:95536508 | TGAACACATCAGATG[A/G]AACACAAAGTGGAGA | 51666 |
rs753611042 | snp | C/T | | | | | GRCh38.p7 | 7:95461542 | TTGATTTAACAGGCT[C/T]ATAGGCAGAAGAGAC | 51666 |
rs753626720 | snp | C/T | 1.65299e-05 | 0.00287483 | missense | ASB4 | GRCh38.p7 | 7:95527858 | AAGATGAGGAGACGC[C/T]CTTGCACACGGCTGC | 51666 |
rs753707347 | snp | A/G | | | | | GRCh38.p7 | 7:95461336 | ACCTCTTGCATCAGC[A/G]TGCCCTGGATGTAAA | 51666 |
rs753730669 | snp | A/T | | | | | GRCh38.p7 | 7:95460375 | AAAATATGGGAAAGT[A/T]TGGAACTTCTTAGAC | 51666 |
rs753742474 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95491606 | AATGAATCTGCCTCA[C/T]CAGTTAATTGTGTTT | 51666 |
rs753744287 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95506068 | TGGCTAATTTTTAAA[A/C]AATTATTTTTAGTAG | 51666 |
rs753769496 | snp | A/C/G | 3.29768e-05 | 0.00406048 | synonymous-codon, intron-variant | ASB4 | GRCh38.p7 | 7:95537642 | TCTCATGCACTTATC[A/C/G]AGATGTGCCATTAGA | 51666 |
rs753855421 | snp | A/G | 1.66418e-05 | 0.00288455 | missense, intron-variant | ASB4 | GRCh38.p7 | 7:95537745 | CTTTTAGAGCCAGAG[A/G]GAATTATTTATTAAG | 51666 |
rs753883890 | in-del | -/AC | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484949 | TCTGTTTCTATTTAC[-/AC]ACACACATATATATA | 51666 |
rs753969029 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513564 | CTGTTTTTAACTCAA[A/G]GTTTGCTGATTTACA | 51666 |
rs753995273 | in-del | -/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95499865 | ACGGGATACATCCTC[-/T]TTTTTTTTTTTTTTT | 51666 |
rs754019007 | snp | A/G | | | | | GRCh38.p7 | 7:95481913 | TTTTTAAGAGCTGAG[A/G]AGACAGGAATTTCTG | 51666 |
rs754072648 | in-del | -/TCTTTCTCTT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515162 | TTCTTTCTTTCTTTC[-/TCTTTCTCTT]TCTTTCTTTCTTTCT | 51666 |
rs754091739 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95514194 | TCACCCTCTCTTAAC[A/G]TCATTTCTTTCTCTA | 51666 |
rs754093096 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95501788 | GGGAGACTACCTAGA[A/G]ATGAGAAGGAAGAAA | 51666 |
rs754102299 | snp | C/T | 1.64925e-05 | 0.00287158 | missense | ASB4 | GRCh38.p7 | 7:95528038 | TGGTCTGCCGCATGC[C/T]GCTTGACTACAAAGC | 51666 |
rs754119158 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95500188 | ACATTTTCATAAGAA[A/T]GGAGAAGGAATGGGA | 51666 |
rs754172375 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95487414 | TGCTAAACTAATTTT[C/T]AAGATGTTTTTAAAA | 51666 |
rs754199106 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95521704 | AAAAAAAAAAACAGT[A/T]CTCTATTCAAAGACA | 51666 |
rs754299731 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95534960 | CCAGATGTGCTGCCA[A/G]CTGGCTTCATCTTAC | 51666 |
rs754308698 | in-del | -/TT | | | | | GRCh38.p7 | 7:95477736 | CCCTTAACAAGAACC[-/TT]TTTTTTTTTTTTTGC | 51666 |
rs754311551 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95487103 | CTATAAATCATCAGT[A/G]TAATACATTTCCAGA | 51666 |
rs754349874 | in-del | -/T | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539091 | TTGTTCTTGCTATAA[-/T]CACTTTTAGATAAGC | 51666 |
rs754354081 | snp | C/T | 4.97269e-05 | 0.00498608 | missense | ASB4 | GRCh38.p7 | 7:95536471 | CTTGTCCTAAAGCAA[C/T]TGAAGTTGTAGTCAA | 51666 |
rs754371535 | snp | A/T | | | | | GRCh38.p7 | 7:95476398 | TTCTTTTTTATATTT[A/T]AAAAAAAATTTATAG | 51666 |
rs754393174 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95519243 | GTTCATGACATACTC[A/G]ACACTGTACAAAATT | 51666 |
rs754394897 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95522143 | AGTTCTCTCTTTTAT[A/G]TATAAACACAAAATA | 51666 |
rs754432763 | snp | C/T | 1.64942e-05 | 0.00287173 | missense | ASB4 | GRCh38.p7 | 7:95495805 | TCCTGGGCCACAGGC[C/T]TCCATCTCTCTGTCT | 51666 |
rs754526569 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95523440 | TTAACTAAAAAAGAA[A/T]TACCATTAGTTAATA | 51666 |
rs754585089 | snp | A/G | 1.64939e-05 | 0.0028717 | missense | ASB4 | GRCh38.p7 | 7:95495940 | AATGTGGATTGTGTT[A/G]AGATCCTCTGTGATC | 51666 |
rs754642300 | snp | A/G | 0.000115587 | 0.00760132 | missense | ASB4 | GRCh38.p7 | 7:95496027 | ACAACTCCAAGTTCC[A/G]TTCTCTGTGCCAAGC | 51666 |
rs754662025 | snp | C/T | | | | | GRCh38.p7 | 7:95482410 | TGAAGTCATGTTCCC[C/T]GTGGCCTTTGACCTT | 51666 |
rs754672011 | snp | G/T | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539920 | AACAAAGTAAAACAA[G/T]ATCACACCCTGGAAC | 51666 |
rs754675055 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95512733 | GAAGAATGAAATTAG[G/T]GCCTATAGCTAGAAG | 51666 |
rs754722368 | in-del | -/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95512626 | CAAAGGTACATAAAA[-/T]CTACACATTTATTTA | 51666 |
rs754752873 | snp | A/T | | | | | GRCh38.p7 | 7:95461556 | TCATAGGCAGAAGAG[A/T]CTTGCCTTGTTTCAG | 51666 |
rs754757355 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95514637 | ATTTGAAAAGATAGT[C/T]TCAGATGATTAGTCA | 51666 |
rs754799002 | snp | A/G | 4.97038e-05 | 0.00498492 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95536517 | CAGATGGAACACAAA[A/G]TGGAGAAGAGCTATC | 51666 |
rs754816658 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95502016 | TAAAATTAAAAGGCA[A/T]TCATAAAACTGGGGA | 51666 |
rs754858043 | snp | A/T | | | intron-variant, nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471640 | TAATTTTGGCCCTTA[A/T]TTGAGGTCCTAGCTT | 51666 |
rs754877074 | snp | C/T | | | | | GRCh38.p7 | 7:95460064 | ATTTGTCCACCATGA[C/T]TGTAAGTTTCCTGAG | 51666 |
rs754882832 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95516197 | ATTAATTTCCTTCAA[C/T]GAAAACACCTTTCTG | 51666 |
rs755007826 | snp | A/C/G | 0.000100865 | 0.00710099 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95537761 | GAATTATTTATTAAG[A/C/G]CTTATGAGACAGCAG | 51666 |
rs755012931 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95503538 | TGGTTCATGGTTAAT[A/G]AAATGCTGCTCTTCA | 51666 |
rs755060721 | snp | A/G | 3.30164e-05 | 0.00406289 | missense | ASB4 | GRCh38.p7 | 7:95527876 | TGCACACGGCTGCCC[A/G]CTTCGGCCTTTCGGA | 51666 |
rs755080092 | snp | C/T | | | | | GRCh38.p7 | 7:95477288 | CTTCGTTATTTGAAG[C/T]TGTGTTTGTTAATAC | 51666 |
rs755106595 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95522637 | ACTTATCTGTGTTGG[A/T]CCTCCCGTTTAGTAC | 51666 |
rs755124294 | snp | C/T | 1.69278e-05 | 0.00290923 | intron-variant | ASB4 | GRCh38.p7 | 7:95486179 | AACATATAGGTGTTA[C/T]TGTAGAACTGTTAGA | 51666 |
rs755129122 | in-del | -/A | | | | | GRCh38.p7 | 7:95466639 | AGACATTTTATGTTT[-/A]TTGCCAGTGTATTAG | 51666 |
rs755154323 | snp | C/T | | | | | GRCh38.p7 | 7:95478633 | CTTTAAATACTCTTA[C/T]ATGAAAGGCAGCTGG | 51666 |
rs755312539 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95511126 | GATGAAAGCTCAGAA[C/T]TGGATGCTAAGAATC | 51666 |
rs755364481 | snp | G/T | | | | | GRCh38.p7 | 7:95467496 | GGATAGGGTATGCTA[G/T]AGGACAGAGATCACA | 51666 |
rs755367793 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95497261 | ATGGAAGCAGGGAGA[A/C]CAGTAGGGAAGCTAT | 51666 |
rs755413103 | snp | A/C | | | | | GRCh38.p7 | 7:95465429 | AGAAATATGTTCAAA[A/C]TACTATGGTAGTGCA | 51666 |
rs755447313 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485755 | ATATATTACTGAATG[A/G]ATCAGTTAATATATA | 51666 |
rs755464525 | snp | G/T | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484731 | AAATGCAATTTATTT[G/T]CATTCTCTTTAGAAC | 51666 |
rs755470845 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95531304 | GTCATTCTTCATGAC[C/G]TTAGCTCTAGAAGAC | 51666 |
rs755490268 | snp | C/G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95519312 | AGAACATGCAGAAAA[C/G/T]GAAAAGCCCTGAATA | 51666 |
rs755494783 | snp | A/G | 1.64947e-05 | 0.00287177 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95528201 | TGCCATCCAGTACGT[A/G]CTGAAGGTCACCTCC | 51666 |
rs755498507 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95499284 | GATAAAGAGTATATA[G/T]AGAGAAAAGTGAATC | 51666 |
rs755525970 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95517858 | CAATAGAAAGAAATT[A/G]GAGGTTAGCTAAAAG | 51666 |
rs755548825 | snp | C/G | 1.65151e-05 | 0.00287355 | missense | ASB4 | GRCh38.p7 | 7:95528277 | AACCATGGGGCTGCC[C/G]GAATATACCCTCCAC | 51666 |
rs755565436 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95501304 | AATGTAAAGGGGGCC[A/G]TGCCTTTTAAAAGAC | 51666 |
rs755599246 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95495646 | ATCCCCTCTCCACCC[C/T]ACTTTTATAAATGTG | 51666 |
rs755679889 | in-del | -/C | 1.64999e-05 | 0.00287222 | frameshift-variant | ASB4 | GRCh38.p7 | 7:95527953 | ATGCCCACATGGAGA[-/C]CCCCCCTGGCCATCG | 51666 |
rs755684754 | snp | C/T | | | | | GRCh38.p7 | 7:95465901 | TATGAGTAACCACTG[C/T]ACTCCAGCCTAGGCA | 51666 |
rs755719954 | snp | C/T | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95483456 | AGACTGATCATTTAC[C/T]TAAAGAGACTGCTAA | 51666 |
rs755737752 | snp | A/C | 1.65869e-05 | 0.00287979 | intron-variant, stop-gained | ASB4 | GRCh38.p7 | 7:95528315 | TAAGGTGAGGCTCTG[A/C]CCAGTGGTCAGCAGG | 51666 |
rs755760140 | snp | A/T | | | | | GRCh38.p7 | 7:95467345 | ATTTCCGAACCCTTA[A/T]TCCTTTTCACGAAAA | 51666 |
rs755810093 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95532658 | GAATGTTTCTGCTGA[A/G]GTGGCTTACAGATGA | 51666 |
rs755923726 | snp | A/C | 1.68596e-05 | 0.00290336 | intron-variant | ASB4 | GRCh38.p7 | 7:95496063 | GTTTGGAGAGGTAAG[A/C]CTTTCTGGGTGGCCA | 51666 |
rs755944858 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95517511 | CCAAAGTGAGGCAAA[A/C]ATTTAGGGAGTGAGA | 51666 |
rs755952574 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95490243 | AAGCTCTTATTTCCA[C/T]TCTCTGAATGAATAA | 51666 |
rs756033810 | snp | C/G | 1.77325e-05 | 0.00297758 | intron-variant | ASB4 | GRCh38.p7 | 7:95537531 | TTGATGTAAACTGTG[C/G]GGCCTTGCTAACTTT | 51666 |
rs756039367 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95536216 | TTAATAGGTCTGTGG[A/G]TTCTGGTTTTTTTTT | 51666 |
rs756065374 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95504528 | GCATAAATCTGACCA[C/T]GTTAGACATTTGCAA | 51666 |
rs756094625 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95537472 | AGAGACCCTAGGAAG[C/T]TGCCATTACGTATAG | 51666 |
rs756139564 | in-del | -/A | | | intron-variant | ASB4 | GRCh38.p7 | 7:95521688 | CAGCAGTTGAAATTA[-/A]AAAAAAAAAAACAGT | 51666 |
rs756169938 | in-del | -/TAAT | | | | | GRCh38.p7 | 7:95477642 | ACTTCGCTTTGCGAC[-/TAAT]TAATTATGCAATTTT | 51666 |
rs756184119 | snp | A/C | | | | | GRCh38.p7 | 7:95480812 | GCTTTAAGCCAATAC[A/C]TTTTGAGGTTATTTG | 51666 |
rs756223500 | snp | C/T | | | | | GRCh38.p7 | 7:95467638 | ATATTACTTAATACA[C/T]TTTAAATCAAATTTA | 51666 |
rs756298434 | snp | C/G | 1.64996e-05 | 0.0028722 | missense | ASB4 | GRCh38.p7 | 7:95527967 | GACCCCCCTGGCCAT[C/G]GCCGCCTACTGGGCC | 51666 |
rs756369625 | in-del | -/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95498526 | TGTAACTTTTACTCC[-/T]TTAAAGAAATGGGTT | 51666 |
rs756475863 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95500109 | AGGGAGTTCGGATGG[C/T]TTTTCCCCTCAACAA | 51666 |
rs756512427 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95489713 | CGATATAAAGAAAAC[A/G]TAAAGAATGACTTTC | 51666 |
rs756520753 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95532444 | GAAAGTGACACCCCA[A/G]GGAGCCAAGATTGGG | 51666 |
rs756538648 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95516894 | GCTTCTGTGACTTCA[A/G]ATGTCATCAAATGGT | 51666 |
rs756542261 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95519517 | GCCTATACCAGCCCA[G/T]CAGTGTTTTGTACTG | 51666 |
rs756543994 | in-del | -/CCTACTACA | | | | | GRCh38.p7 | 7:95476190 | ACACATCTGTCGGTC[-/CCTACTACA]CCTACTACACCTATC | 51666 |
rs756627493 | snp | A/G | | | downstream-variant-500B, intron-variant | ASB4 | GRCh38.p7 | 7:95540403 | CAAAAGAAAGTAAAG[A/G]GTAACTGTGGCCAAA | 51666 |
rs756644940 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95487169 | TAATTTACTGTCCTC[C/T]GATTGTCAGTTCTGA | 51666 |
rs756653086 | snp | C/G | 2.34189e-05 | 0.00342183 | intron-variant, utr-variant-3-prime | ASB4 | GRCh38.p7 | 7:95528414 | TCCTGGGCTAACTAC[C/G]TCTGATCCTCTTTGA | 51666 |
rs756741824 | snp | A/G | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484647 | TCATTGTAAGTTTTT[A/G]AAAATTCATGTTTTT | 51666 |
rs756746073 | in-del | -/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95495388 | AGTTTTTTAAAAAAA[-/T]ATCCTTGAAGCATCT | 51666 |
rs756763798 | snp | A/T | 3.30934e-05 | 0.00406763 | missense | ASB4 | GRCh38.p7 | 7:95536485 | ATTGAAGTTGTAGTC[A/T]ATGCCTATGAACACA | 51666 |
rs756768517 | in-del | -/A | 6.59593e-05 | 0.00574241 | frameshift-variant | ASB4 | GRCh38.p7 | 7:95495873 | CACAATGCTACAATC[-/A]AACTGTAGACCCAAT | 51666 |
rs756824320 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95531069 | ATGCAGACTCAGTCC[C/T]TCCCCAGAAGGAAGT | 51666 |
rs756838332 | snp | C/G | 1.64898e-05 | 0.00287135 | intron-variant | ASB4 | GRCh38.p7 | 7:95495707 | CAAAACAGGGAGAAA[C/G]CCTAGGTCAAGAAGT | 51666 |
rs756866422 | snp | A/G | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472650 | TCTGCCAAGGTCCAC[A/G]TGCATAGCCTCAAGC | 51666 |
rs756877200 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95517661 | ATATAGTAGAGAGGT[A/G]TGGTAACTGGAAGGT | 51666 |
rs756893922 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485582 | TTGTCAGAGCAAGAC[A/G]CTGGATCTCCAGCCA | 51666 |
rs756975442 | snp | A/G | | | synonymous-codon | ASB4 | GRCh38.p7 | 7:95536481 | AGCAATTGAAGTTGT[A/G]GTCAATGCCTATGAA | 51666 |
rs756977118 | snp | A/T | | | | | GRCh38.p7 | 7:95460393 | GAACTTCTTAGACAC[A/T]TAGTGAATGGCTTTG | 51666 |
rs757029594 | snp | A/T | 0.000201197 | 0.0100279 | stop-lost, intron-variant | ASB4 | GRCh38.p7 | 7:95537758 | AGGGAATTATTTATT[A/T]AGCCTTATGAGACAG | 51666 |
rs757037340 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95504807 | TGACTCTAAAAGGCC[A/G]TGTCTTCTGGTCACT | 51666 |
rs757120300 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95524973 | AGTCTTTTTCCTTTT[C/T]GCCAAATAAATTCTG | 51666 |
rs757155707 | snp | A/G | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538552 | TGCTTATCTTTCAAA[A/G]TTGTGTTTCTGACAT | 51666 |
rs757208378 | snp | C/G | 1.71714e-05 | 0.00293008 | intron-variant | ASB4 | GRCh38.p7 | 7:95496087 | GTGGCCAACATTGTT[C/G]TCTGCTTGTACACTC | 51666 |
rs757210569 | snp | A/G | 1.66924e-05 | 0.00288893 | missense, intron-variant | ASB4 | GRCh38.p7 | 7:95537751 | GAGCCAGAGGGAATT[A/G]TTTATTAAGCCTTAT | 51666 |
rs757227231 | snp | A/G | | | | | GRCh38.p7 | 7:95480965 | TATCTAATTAACCTG[A/G]AAAAAACCATATAAA | 51666 |
rs757244965 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95512742 | AATTAGGGCCTATAG[A/C]TAGAAGGGGAACTCA | 51666 |
rs757263911 | snp | C/T | 1.65201e-05 | 0.00287398 | missense | ASB4 | GRCh38.p7 | 7:95527863 | GAGGAGACGCCCTTG[C/T]ACACGGCTGCCCACT | 51666 |
rs757323090 | snp | C/T | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95470026 | CACACATGCCTCCTG[C/T]ACAGAGCCCACGAGG | 51666 |
rs757327520 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95499490 | TGATAGCTACCCAGG[G/T]TTAATTAGATGTTCA | 51666 |
rs757340580 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95498841 | GGTATAAGTTATGGG[A/T]TAGGTTCGTCTTTTT | 51666 |
rs757350389 | snp | C/T | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469002 | TTATCTGTAAGAGAG[C/T]TGAAGTTTCTTCACC | 51666 |
rs757411358 | in-del | -/AG | | | intron-variant | ASB4 | GRCh38.p7 | 7:95494822 | TCAGTGGGAGAAAAG[-/AG]AGAGAGAGAGAGGCA | 51666 |
rs757418272 | snp | G/T | 1.64933e-05 | 0.00287165 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95528039 | GGTCTGCCGCATGCT[G/T]CTTGACTACAAAGCC | 51666 |
rs757423405 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95487422 | TAATTTTTAAGATGT[C/T]TTTAAAAAGCTTATA | 51666 |
rs757471123 | snp | A/G | 1.65026e-05 | 0.00287246 | missense | ASB4 | GRCh38.p7 | 7:95528154 | CTGGAAGCTGGCGCC[A/G]AAGCCAATCTCATGG | 51666 |
rs757486988 | in-del | -/TT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515197 | TTCTTTCTTTCTTTC[-/TT]TTTCTTTCTTTCTTT | 51666 |
rs757505387 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95501860 | AATGAATTAGGCTTA[C/T]AAGAATCAAGGAGAG | 51666 |
rs757606923 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95533804 | GAGCAAGTTAAAGTA[C/T]ATGAAGATTTAACAC | 51666 |
rs757630809 | snp | C/T | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472942 | CTCAGTACAAGGAAA[C/T]CAAACTGCTAAATCC | 51666 |
rs757648599 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95522255 | AGAGGCTGAACTTTG[A/G]TTTATTAGAACTTTA | 51666 |
rs757660898 | snp | A/T | 3.29864e-05 | 0.00406105 | missense | ASB4 | GRCh38.p7 | 7:95495806 | CCTGGGCCACAGGCC[A/T]CCATCTCTCTGTCTT | 51666 |
rs757673777 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95521213 | CAATACATAAAGAAA[C/T]GTTTCCTTTTTGAAT | 51666 |
rs757719040 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95500808 | TCACTTACTTTGGCA[C/T]ACAAGGTTTTCCTCT | 51666 |
rs757746541 | snp | A/C | | | downstream-variant-500B, intron-variant | ASB4 | GRCh38.p7 | 7:95540251 | TTTGTGTTTACTTAC[A/C]AATAAGACTCTTTTT | 51666 |
rs757757578 | in-del | -/AT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95504354 | ACACAAGTCAACCAC[-/AT]ATGTTAGGAAATTCC | 51666 |
rs757769199 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95509184 | GAAGATAATTATATT[C/T]GGGAAGGAGATTAGG | 51666 |
rs757801459 | snp | C/T | | | | | GRCh38.p7 | 7:95476506 | GCCTAGCTCTTTTAC[C/T]CCCTGGAGCAATCAA | 51666 |
rs757933810 | snp | G/T | | | | | GRCh38.p7 | 7:95460520 | GCTATGCAAAGAGAC[G/T]GGCAGCATTTTGCCC | 51666 |
rs757962480 | snp | A/G | 3.29804e-05 | 0.00406068 | missense | ASB4 | GRCh38.p7 | 7:95495926 | CTTGTGAAATGGCCA[A/G]TGTGGATTGTGTTAA | 51666 |
rs757965652 | snp | G/T | | | downstream-variant-500B | LOC107986823 | GRCh38.p7 | 7:95474965 | TTAAGGAGGAGGGAT[G/T]CAGGAGATACTTTTG | 51666 |
rs757996908 | snp | A/G | 1.65452e-05 | 0.00287616 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95536505 | CTATGAACACATCAG[A/G]TGGAACACAAAGTGG | 51666 |
rs758012899 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95506303 | CAGACCTGCTCCAAT[G/T]AGTTTCAGGTTGATG | 51666 |
rs758050159 | snp | C/T | 1.77824e-05 | 0.00298176 | intron-variant | ASB4 | GRCh38.p7 | 7:95536564 | AGGTAAATAATCGAT[C/T]CCCTTCTAATAGTTT | 51666 |
rs758067988 | snp | C/T | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538046 | AATATTTTTGTAAAA[C/T]TTCTTATATCTTATC | 51666 |
rs758068608 | snp | C/G | | | | | GRCh38.p7 | 7:95461555 | CTCATAGGCAGAAGA[C/G]ACTTGCCTTGTTTCA | 51666 |
rs758073916 | snp | C/T | 1.64931e-05 | 0.00287163 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95495813 | CACAGGCCTCCATCT[C/T]TCTGTCTTGTTTGGC | 51666 |
rs758077555 | in-del | -/TGTGT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95493383 | GTGTGTGTGTGTGTG[-/TGTGT]GTGTATGTGTGTGTG | 51666 |
rs758083536 | in-del | -/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95534785 | TAAAGACAAAAAACA[-/G]GTCATAAATCTCCCA | 51666 |
rs758099057 | snp | A/G | | | | | GRCh38.p7 | 7:95465439 | TCAAAATACTATGGT[A/G]GTGCAAAAGAAGAGT | 51666 |
rs758110515 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95494440 | ATTACAGCTCAAATC[C/T]CTAGGTTGTTTCTCA | 51666 |
rs758149142 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95526433 | CTGCTGTGCTGCCGG[C/T]TGCAACTTTGCAACG | 51666 |
rs758156532 | in-del | -/A | | | intron-variant | ASB4 | GRCh38.p7 | 7:95502178 | AGGAATATTTAAGGG[-/A]AAAAAAAAGAAAAAT | 51666 |
rs758161280 | snp | A/G | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538676 | TTTTTTCTAGATAGT[A/G]TGTCTTTTTGGTATG | 51666 |
rs758207735 | in-del | -/TC | | | | | GRCh38.p7 | 7:95477236 | GGTTTTAATTTTGAT[-/TC]TCTCTCTAGAAAAAC | 51666 |
rs758246681 | snp | A/C | | | | | GRCh38.p7 | 7:95481194 | TGTTGACATTGAGAA[A/C]TTCTGGATCAGACCT | 51666 |
rs758281370 | in-del | -/TTT | 0.0773738 | 0.180832 | intron-variant | ASB4 | GRCh38.p7 | 7:95495739 | AAACTTTCCTTTTCC[-/TTT]TTTTTTTTTTTTTCA | 51666 |
rs758290033 | snp | C/G | | | | | GRCh38.p7 | 7:95478569 | CAATCTAGCATCGTG[C/G]CAGCGACCAAGATTC | 51666 |
rs758295307 | snp | C/T | | | | | GRCh38.p7 | 7:95463528 | CCCCTTAGTGCTGCT[C/T]TTGCGGTAGAGTTCT | 51666 |
rs758300456 | snp | G/T | 0.000445479 | 0.0149178 | intron-variant, utr-variant-3-prime | ASB4 | GRCh38.p7 | 7:95528392 | TCAAGCTTGCTTGAG[G/T]CTTGAGTCCTGGGCT | 51666 |
rs758334435 | in-del | -/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95511643 | CTCCAGCCTGGGCAA[-/C]AAGAGCAAAACTCCG | 51666 |
rs758425345 | snp | C/T | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95470220 | AGTGTAATGTGAACA[C/T]TAAATGTCCAGGCAC | 51666 |
rs758518781 | in-del | -/TGC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95523437 | AATTAACTAAAAAAG[-/TGC]AAATACCATTAGTTA | 51666 |
rs758548015 | snp | A/G | | | intron-variant, nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471559 | GTTGAAGGCTCTTCC[A/G]ACACTGTCAGTGTAC | 51666 |
rs758556758 | snp | C/T | | | | | GRCh38.p7 | 7:95476786 | TCATAAGACAACGGT[C/T]TGTAAAGAATCTGGA | 51666 |
rs758567893 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95488874 | TTTCAGTTATTTTTG[G/T]CTTAATAAGAAAGAC | 51666 |
rs758575115 | snp | A/G | 3.43501e-05 | 0.00414414 | utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485970 | CCAGAGGGAGAGGAA[A/G]GATGGACGGCACCAC | 51666 |
rs758587757 | snp | C/T | 8.24328e-05 | 0.00641947 | missense, intron-variant | ASB4 | GRCh38.p7 | 7:95537646 | ATGCACTTATCGAGA[C/T]GTGCCATTAGAAGAA | 51666 |
rs758598317 | in-del | -/AAAAT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95516363 | GAATTAAAAAGATAA[-/AAAAT]AAAATAAATACAGGG | 51666 |
rs758626681 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95521606 | ACTATTGGGAAAAAG[C/T]TAAAACAACTTTACC | 51666 |
rs758630384 | snp | C/T | 3.29538e-05 | 0.00405904 | missense | ASB4 | GRCh38.p7 | 7:95486075 | TCGGAAAATTGAAGG[C/T]TATTTTGATCCAAAG | 51666 |
rs758678934 | snp | C/T | | | | | GRCh38.p7 | 7:95463441 | TGTCCAGTTGTAATC[C/T]CCAATGTTGGAGGTT | 51666 |
rs758682676 | snp | C/T | 1.64895e-05 | 0.00287132 | missense | ASB4 | GRCh38.p7 | 7:95528065 | AAGCCGAAGTCAATG[C/T]CCGAGATGACGACTT | 51666 |
rs758684791 | snp | A/T | | | | | GRCh38.p7 | 7:95467889 | CCAGCATGAAACAAC[A/T]CACCAATTAACATTT | 51666 |
rs758778262 | snp | C/T | | | | | GRCh38.p7 | 7:95478325 | ATGTTTAAACTGTGC[C/T]GGACGGCGTGTAAAT | 51666 |
rs758833325 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95534640 | GTCTTCTCCTCTGTG[G/T]GTTGCTGATGGTGCT | 51666 |
rs758839589 | snp | A/G | | | | | GRCh38.p7 | 7:95465997 | TTCCCAATTAGAATA[A/G]TGCAATTTAAGTATG | 51666 |
rs758896524 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95497130 | TTGAGGGTCAAAGTG[C/T]AGGGCTCTGAAATGG | 51666 |
rs758930769 | in-del | -/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515306 | TTCTTTCTTTCTTTC[-/T]TTCTTTCTTTCTTCC | 51666 |
rs758941915 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95535598 | AAAGTTGGTTAAGTG[C/T]ATAAACATCCATGTA | 51666 |
rs758973462 | snp | A/G | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95483594 | AGATATAAACAAACT[A/G]TATTATTTTTGTATG | 51666 |
rs759056780 | in-del | -/TT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515168 | TTTCTTTCTCTTTCT[-/TT]CTTTCTTTCTTTCTT | 51666 |
rs759064528 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95523401 | TTTCACCTAATAAAG[A/T]GACAATGAACTAAAT | 51666 |
rs759100808 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95516317 | GTCTTATCTATGGTT[A/C]CTTTGCAAAATTTTA | 51666 |
rs759109786 | snp | A/G | | | | | GRCh38.p7 | 7:95476194 | CATCTGTCGGTCCCT[A/G]CTACACCTATCACAG | 51666 |
rs759116449 | snp | C/T | 3.33684e-05 | 0.00408449 | missense | ASB4 | GRCh38.p7 | 7:95527828 | GGGCGAATGTGAACA[C/T]GAAGACCAACAACCA | 51666 |
rs759136930 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95508835 | CAAAGAGAACACAGA[A/G]AGGGATCTGATGGAG | 51666 |
rs759138265 | snp | A/G | | | | | GRCh38.p7 | 7:95465063 | ATAGGGGAAAATTAA[A/G]TGACACCTCAGAAGA | 51666 |
rs759160158 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95503069 | TCTGAAAATTATATG[C/T]GACTATGCATATCAA | 51666 |
rs759163227 | snp | A/C | | | | | GRCh38.p7 | 7:95477685 | TGTAAGTGAGATGGC[A/C]TCAGTACTTTTTTTC | 51666 |
rs759190374 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95509761 | CTATGATGTGGCTAT[A/G]TCAGGTACTTGAAAA | 51666 |
rs759190727 | snp | C/T | 3.30044e-05 | 0.00406216 | missense, intron-variant | ASB4 | GRCh38.p7 | 7:95537628 | AACTCTCCAAGGACT[C/T]TCATGCACTTATCGA | 51666 |
rs759242362 | snp | A/G | | | downstream-variant-500B | LOC107986823 | GRCh38.p7 | 7:95474980 | TCAGGAGATACTTTT[A/G]CAATATGATCCTTAG | 51666 |
rs759310564 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95496777 | CACTTGATCCCAAGA[A/G]GTCAAGGCTGCAGTG | 51666 |
rs759312007 | snp | A/G | | | | | GRCh38.p7 | 7:95467063 | GATTTTTTTCTGTGA[A/G]CTTATATATACGTAA | 51666 |
rs759350989 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95518228 | TTCTAGTCCACTTGA[A/G]GTTCAGCAGGCATAT | 51666 |
rs759352762 | in-del | -/ATTT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95520982 | ACTTTTCCAAAATTG[-/ATTT]ATTTTTGCTCTTTAC | 51666 |
rs759366199 | snp | C/G | | | | | GRCh38.p7 | 7:95463251 | TTGCCCAGGCTAGTT[C/G]CTACCTCCTGGCCTC | 51666 |
rs759400192 | in-del | -/TTTCT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515373 | TCTTTCTTTTCTTTC[-/TTTCT]TTTCTTTTCTTTTTT | 51666 |
rs759410436 | snp | C/T | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95485373 | GTCCCTGCCCCGGAC[C/T]GTCTCCCCACCTCCT | 51666 |
rs759415954 | snp | A/G | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484262 | GCTTGAGCCTGAGAG[A/G]CAAAGGTTGCAGTGA | 51666 |
rs759416447 | snp | A/C/T | 9.50103e-05 | 0.00689186 | utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485934 | TCGGTGCTGTTCTCT[A/C/T]GATAAATCACAACAA | 51666 |
rs759432039 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95529255 | GCATTTTACCTGAAA[A/G]TAAATCAAATAATAC | 51666 |
rs759440405 | snp | C/T | 1.64811e-05 | 0.00287059 | missense | ASB4 | GRCh38.p7 | 7:95486059 | CTAAAGTCCAATGAC[C/T]TCGGAAAATTGAAGG | 51666 |
rs759465469 | snp | C/T | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473182 | TTTCTCACCTCTATC[C/T]GTCAGAGGAGTCAGA | 51666 |
rs759469934 | snp | C/G | 1.64906e-05 | 0.00287142 | missense | ASB4 | GRCh38.p7 | 7:95495873 | CCACAATGCTACAAT[C/G]AACTGTAGACCCAAT | 51666 |
rs759504266 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95507502 | TGTTCTGTATTCTCA[C/T]AGCACATTGTAGCTT | 51666 |
rs759538753 | snp | C/T | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472376 | TACTATTTGAACAAA[C/T]CTCAATAATATTTGA | 51666 |
rs759660622 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95533563 | ATCTCTTGATCTTCA[A/T]GACCCCCTTGATAAT | 51666 |
rs759702680 | in-del | -/A | | | | | GRCh38.p7 | 7:95475747 | TGTCTTTATAAAACC[-/A]AATCATGTATTCCAG | 51666 |
rs759736332 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95537428 | ACTGCTCCCATTTCA[A/C]TATTGCGTTTAATTT | 51666 |
rs759785860 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95525786 | AACTTCTCTAGGGCA[A/G]AATACTGATAAACAC | 51666 |
rs759796838 | snp | C/G | | | | | GRCh38.p7 | 7:95461068 | CCTCATGGAGAACAT[C/G]TGCTAGGGCAGTGCA | 51666 |
rs759829404 | snp | A/G | 6.60939e-05 | 0.00574827 | missense | ASB4 | GRCh38.p7 | 7:95495776 | ACTGGTTGCCTAGCT[A/G]TAAATTGAAGTCTTC | 51666 |
rs759858881 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95524681 | TAATTACTTAAGTTA[C/T]GTTAAAATCATACTA | 51666 |
rs759866214 | snp | A/T | | | | | GRCh38.p7 | 7:95468684 | TGTACAAAATTCAAT[A/T]GATCAGACATAGAGC | 51666 |
rs759891800 | snp | A/G | | | missense | ASB4 | GRCh38.p7 | 7:95528268 | CTCCTGTTGAACCAT[A/G]GGGCTGCCCGAATAT | 51666 |
rs759917140 | in-del | -/A | | | intron-variant | ASB4 | GRCh38.p7 | 7:95521019 | GCAAATTTTGTGGGG[-/A]AAAATGTTTGAATTG | 51666 |
rs759938492 | snp | G/T | | | | | GRCh38.p7 | 7:95481648 | CCATGATAAACCAAG[G/T]AGCCATTTGTGTTCC | 51666 |
rs759982680 | snp | C/T | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484900 | CCCTTACTAGATTCA[C/T]CAAGTCTTTAAGTTT | 51666 |
rs760017807 | snp | G/T | 6.59914e-05 | 0.00574381 | missense | ASB4 | GRCh38.p7 | 7:95527924 | TGGAACACGGGGCCA[G/T]AGTGGACAGCGTGAA | 51666 |
rs760067905 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513099 | TAAGAGATTCTACCC[A/C]CCATTGTTAGCTTTG | 51666 |
rs760230175 | in-del | -/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515156 | TTGTTTTTCTTTCTT[-/T]CTTTCTCTTTCTCTT | 51666 |
rs760239917 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95499983 | GGTTCACGCCATTCT[A/C]CTGCCTCAGCCTCCC | 51666 |
rs760254522 | snp | C/T | 8.24885e-05 | 0.00642164 | missense | ASB4 | GRCh38.p7 | 7:95527942 | TGGACAGCGTGAATG[C/T]CCACATGGAGACCCC | 51666 |
rs760270062 | in-del | -/T | | | | | GRCh38.p7 | 7:95477737 | CCTTAACAAGAACCT[-/T]TTTTTTTTTTTTTGC | 51666 |
rs760307585 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95530692 | CAGACCATATATGTC[A/G]CCTTGTAAGCTGTGG | 51666 |
rs760326484 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95498779 | GTTTTGTCATTTCAG[A/G]TTTTACTTTTAGGTG | 51666 |
rs760386387 | in-del | -/TGTA | | | intron-variant | ASB4 | GRCh38.p7 | 7:95493389 | GTGTGTGTGTGTGTG[-/TGTA]TGTGTGTGTGTGTGT | 51666 |
rs760432759 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95516040 | TGGTCCAGGCCTCCT[C/T]TTGCCTTTGAGTCCA | 51666 |
rs760437887 | snp | C/T | | | | | GRCh38.p7 | 7:95468337 | GGCAGAAATTGCATT[C/T]ATTGACTTGTAAAGC | 51666 |
rs760504462 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95486701 | AATGAGTTTTCAGTT[C/G]AGGCACAAAAGCTGA | 51666 |
rs760544220 | in-del | -/CTC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515422 | TTTTCCTTTCTCTCT[-/CTC]TTTTTTTTTTAAGAC | 51666 |
rs760562210 | snp | A/G | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473366 | ATCTCCATTTTAGAC[A/G]TGAAGGACCCAAGGC | 51666 |
rs760573737 | snp | C/G | 1.76868e-05 | 0.00297373 | intron-variant, missense | ASB4 | GRCh38.p7 | 7:95528361 | ATGGCAGCCTTGTCT[C/G]AAATCTCCAAGTAAC | 51666 |
rs760574201 | snp | C/T | 1.64773e-05 | 0.00287026 | missense | ASB4 | GRCh38.p7 | 7:95486069 | ATGACTTCGGAAAAT[C/T]GAAGGCTATTTTGAT | 51666 |
rs760591550 | snp | C/G | 1.6601e-05 | 0.00288101 | missense, intron-variant | ASB4 | GRCh38.p7 | 7:95537736 | AAGTACTTGCTTTTA[C/G]AGCCAGAGGGAATTA | 51666 |
rs760627167 | snp | A/G | 1.66283e-05 | 0.00288338 | missense | ASB4 | GRCh38.p7 | 7:95486156 | TGGCATCTTATAAAC[A/G]AGGTAAAAACATATA | 51666 |
rs760642553 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95518715 | ATGTACAAATCTTTA[A/G]CAGGGATTCCACTGC | 51666 |
rs760649886 | in-del | -/GATTTATGTTCTCC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95535419 | CCCCTCAGAAAGGTT[-/GATTTATGTTCTCC]GATTTATGTTCTCCG | 51666 |
rs760657389 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95492419 | CTTGGAGGTAATTCT[A/G]TTCTGCTTCCACAAA | 51666 |
rs760669595 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95529280 | TAATACTATACTTAG[C/G]TTTCCCCCTTGCTCT | 51666 |
rs760692388 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95506048 | ACAGGCACATGGGCC[G/T]TGCCTGGCTAATTTT | 51666 |
rs760693855 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95520210 | ATGTGCCTCTGACAC[A/G]GTGGTGGGTACTGCA | 51666 |
rs760776325 | snp | C/T | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538508 | TATAAAGTGATGGGG[C/T]AAGAGTACAGGTGCA | 51666 |
rs760833458 | snp | A/C | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539150 | GTTAAAGCAGAAGTA[A/C]ATTGCAAACAAATCT | 51666 |
rs760847477 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95494051 | AGTACAATGCAAATG[C/T]TGTTTTTTGTGGAGT | 51666 |
rs760930817 | in-del | -/TTTT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95495739 | AAACTTTCCTTTTCC[-/TTTT]TTTTTTTTTTTTCAG | 51666 |
rs760946352 | snp | C/G | | | | | GRCh38.p7 | 7:95482923 | TTCGAGGACACTGAG[C/G]TTAGCGGCTCAGCAT | 51666 |
rs760958467 | snp | A/G | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469809 | TGGCATACTTTATAC[A/G]CTCAGAATTGAGTAA | 51666 |
rs760972003 | snp | A/G | | | | | GRCh38.p7 | 7:95481867 | ATGAAACAGTAATAA[A/G]AAGCTCATCTTATAG | 51666 |
rs761020955 | in-del | -/T | 1.66023e-05 | 0.00288113 | frameshift-variant | ASB4 | GRCh38.p7 | 7:95536526 | ACAAAGTGGAGAAGA[-/T]GCTATCCCCGATGAT | 51666 |
rs761066510 | snp | A/G | | | | | GRCh38.p7 | 7:95482929 | GACACTGAGGTTAGC[A/G]GCTCAGCATTAGAGA | 51666 |
rs761176544 | snp | G/T | 1.65121e-05 | 0.00287329 | missense | ASB4 | GRCh38.p7 | 7:95495786 | TAGCTATAAATTGAA[G/T]TCTTCCTGGGCCACA | 51666 |
rs761245015 | snp | C/T | 1.6646e-05 | 0.00288491 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95536460 | GGCCTGCCATTCTTG[C/T]CCTAAAGCAATTGAA | 51666 |
rs761276754 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95488593 | GAATAGGACCCATTT[C/T]TGTGTGGCCTTAAAA | 51666 |
rs761306107 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95534819 | TTACTGTCATAGTAC[C/T]AAACCCAGTGCTCAA | 51666 |
rs761320648 | snp | C/G | | | | | GRCh38.p7 | 7:95468476 | TGTGGAACGCACAAT[C/G]GTTTCACAAATAAAT | 51666 |
rs761362745 | in-del | -/CC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95505687 | TTCCTCTATCCGTGT[-/CC]CCCCCCCCCCAAATA | 51666 |
rs761365566 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95499029 | TTTTTTCCCTAATGC[C/T]CCACTGACTTGATTG | 51666 |
rs761382731 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513064 | TGGCTATAGAAGGAA[A/G]GTCAGAGAGATAGGA | 51666 |
rs761469322 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95496953 | CTATAGGAAATAGCT[C/T]GAGCAAAATTGCTAA | 51666 |
rs761483607 | in-del | -/TCTTTCTT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515168 | CTTTCTTTCTCTTTC[-/TCTTTCTT]TCTTTCTTTCTTTCT | 51666 |
rs761511681 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95521584 | CTGCACAGTTTGAAA[A/G]ATATTTACTATTGGG | 51666 |
rs761525802 | snp | A/C | 1.64953e-05 | 0.00287182 | missense | ASB4 | GRCh38.p7 | 7:95528020 | ACAGCACGGAGCACC[A/C]CCTGGTCTGCCGCAT | 51666 |
rs761613193 | snp | A/T | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469367 | CATTTAGTTTTCCTC[A/T]TTCAATAACAATTTG | 51666 |
rs761635646 | snp | C/T | 1.67832e-05 | 0.00289677 | intron-variant | ASB4 | GRCh38.p7 | 7:95495754 | TTTTTTTTTTTTTTT[C/T]CAGGTTACTGGTTGC | 51666 |
rs761637463 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95520715 | AGTCTTTGGTTCCAA[C/T]ACCTTTATTAATAGT | 51666 |
rs761647020 | snp | A/C | | | | | GRCh38.p7 | 7:95461380 | GAGATCATTTTGGAA[A/C]GTTAAGATTTAACGA | 51666 |
rs761647111 | snp | C/T | | | | | GRCh38.p7 | 7:95475706 | TATTTAATAGCTAAA[C/T]TGCTCTACTTGCATT | 51666 |
rs761666207 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95488046 | AAACTTCATCTTTCT[G/T]AAAAGTTTCTTCAGG | 51666 |
rs761686052 | in-del | -/A | 1.64876e-05 | 0.00287116 | frameshift-variant, intron-variant | ASB4 | GRCh38.p7 | 7:95537687 | CAGATGCCATAGAGC[-/A]ATTCCTTTGCTTTCC | 51666 |
rs761695783 | in-del | -/AAAC | | | | | GRCh38.p7 | 7:95465939 | GATACCCTGTTTCTG[-/AAAC]AAACAAACAAACAAA | 51666 |
rs761717446 | snp | C/T | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539372 | GTGTAAGAAAAGTCA[C/T]AGGTGGATACAATAA | 51666 |
rs761762190 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95507186 | TGGCTGCACCTTTCA[A/T]CTGAGGAATCTCTGA | 51666 |
rs761771613 | snp | A/T | | | | | GRCh38.p7 | 7:95462625 | TGTGACCTTATTTAC[A/T]CGTAAAAGGCTTACA | 51666 |
rs761821471 | snp | A/G | | | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471947 | GCACAACTACTAGTA[A/G]TATTGAGTCTATACG | 51666 |
rs761846987 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95494137 | TAAATACCCAGGAGT[A/G]GCATGTCTCTAGTGT | 51666 |
rs761848418 | in-del | -/AC | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484311 | TGCTCCAGTCTGGTG[-/AC]AGAGTGAGATCCTGT | 51666 |
rs761851472 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95527027 | GTACAAAAAATTCCT[A/G]TTTCTAACATCCTTT | 51666 |
rs761935325 | snp | A/G | 1.64991e-05 | 0.00287215 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95528240 | TGCTGCCCAGCCTGA[A/G]ATCTGCTACCAGCTC | 51666 |
rs761971361 | in-del | -/A | 6.86772e-05 | 0.00585951 | intron-variant | ASB4 | GRCh38.p7 | 7:95486203 | GTTAGAAAATGATTT[-/A]AAAAAAATGCACAGT | 51666 |
rs762018311 | snp | A/G | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472125 | TGACACTAGGTGGGG[A/G]CTCAGTAGCTCATGC | 51666 |
rs762024665 | snp | C/G | | | | | GRCh38.p7 | 7:95482967 | GACCCCTTGGGAACT[C/G]CATTCCTTAGCTTAG | 51666 |
rs762062798 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95502946 | ATTTCATGTTGTTAC[C/T]GCCATACCATGCAGA | 51666 |
rs762150698 | snp | G/T | 1.64857e-05 | 0.00287099 | stop-gained | ASB4 | GRCh38.p7 | 7:95495988 | TGCTACTCCTTAAGT[G/T]GACACACAGCTTTGC | 51666 |
rs762179667 | in-del | -/G | | | downstream-variant-500B, intron-variant | ASB4 | GRCh38.p7 | 7:95540526 | CATCTCTGTCCTCCT[-/G]GGGTTTTTCATTTTC | 51666 |
rs762240646 | snp | G/T | 1.65855e-05 | 0.00287967 | synonymous-codon, intron-variant | ASB4 | GRCh38.p7 | 7:95537603 | CCACTCTCTCTTTAC[G/T]GTGTGCTGTAACTCT | 51666 |
rs762340074 | snp | A/G | 1.74674e-05 | 0.00295523 | intron-variant | ASB4 | GRCh38.p7 | 7:95536558 | ACTTGGAGGTAAATA[A/G]TCGATTCCCTTCTAA | 51666 |
rs762353775 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95535727 | ATTAAACAGAGTGTG[C/T]TAAGAGCTAACTGAA | 51666 |
rs762395018 | snp | A/G | 4.94719e-05 | 0.00497328 | missense | ASB4 | GRCh38.p7 | 7:95495907 | AAAACCCCTCTTCAC[A/G]TGGCTTGTGAAATGG | 51666 |
rs762450242 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95523655 | TTCAAATGTTTCAGC[C/T]TAATAATTCTATTTT | 51666 |
rs762508235 | snp | C/T | 1.6516e-05 | 0.00287362 | missense, intron-variant | ASB4 | GRCh38.p7 | 7:95537619 | GTGTGCTGTAACTCT[C/T]CAAGGACTCTCATGC | 51666 |
rs762509577 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95486943 | GGTTAATTGGGGGAA[C/T]GTGAGTAGTTAGATC | 51666 |
rs762533207 | snp | A/T | | | | | GRCh38.p7 | 7:95475978 | TATATCAAGATCCCA[A/T]GATCCTATTTCAAAT | 51666 |
rs762535540 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95501284 | GCAGAATGTAGCATG[C/G]GGGCAATGTAAAGGG | 51666 |
rs762548918 | snp | C/T | | | | | GRCh38.p7 | 7:95479913 | TCCCTTCCTGTTTCT[C/T]GTCTCAGGGTCTTAG | 51666 |
rs762581954 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95507346 | CTGGGGATGCAAATA[C/G]AGCATATCTGCTATC | 51666 |
rs762655345 | in-del | -/AGGTAA | 5.10408e-05 | 0.00505151 | intron-variant | ASB4 | GRCh38.p7 | 7:95536549 | CCGATGATGACTTGG[-/AGGTAA]ATAATCGATTCCCTT | 51666 |
rs762672350 | snp | C/T | 1.903e-05 | 0.00308458 | utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485926 | CTGTTTGCTCGGTGC[C/T]GTTCTCTCGATAAAT | 51666 |
rs762729029 | in-del | -/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95494255 | CATCATTTCTTGTAA[-/G]GGGCAATGCCCAGCA | 51666 |
rs762740868 | snp | C/T | | | | | GRCh38.p7 | 7:95477557 | GGAGATGCAAAACTA[C/T]AGAAAACTACAGAAA | 51666 |
rs762755390 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95509667 | ACAGCATTGGCACTA[C/T]ATATAAAGGAAATTG | 51666 |
rs762793152 | snp | C/T | | | | | GRCh38.p7 | 7:95464830 | GTTCTGTGCACCAGC[C/T]TGGAAGACATTTTTA | 51666 |
rs762856021 | snp | A/G | | | intron-variant, utr-variant-3-prime | ASB4 | GRCh38.p7 | 7:95528799 | AGCACACTGTTATAA[A/G]CATTTTGTATGTCTT | 51666 |
rs762860453 | snp | G/T | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539785 | CATATTGGGTACAGT[G/T]TACACTGCTCCAGTG | 51666 |
rs762907403 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95516057 | TGCCTTTGAGTCCAG[A/C]ACAGACAGAATTTTG | 51666 |
rs763044789 | snp | C/G | 3.30044e-05 | 0.00406216 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95528258 | CTGCTACCAGCTCCT[C/G]TTGAACCATGGGGCT | 51666 |
rs763053756 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95530305 | CCCTGTCTCTAATAA[A/C]ATACAAAAAATTAGC | 51666 |
rs763088336 | snp | A/G/T | 3.34881e-05 | 0.00409184 | intron-variant | ASB4 | GRCh38.p7 | 7:95486169 | ACAAGGTAAAAACAT[A/G/T]TAGGTGTTATTGTAG | 51666 |
rs763089877 | in-del | -/A | | | intron-variant | ASB4 | GRCh38.p7 | 7:95524290 | AAAGACAGACATAAT[-/A]AAAATGAACAAATGA | 51666 |
rs763099294 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513231 | CTTAGCCCACTGTCA[A/G]GGTTTTTTTTGTTTT | 51666 |
rs763115328 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95503306 | GAGGAGAAAGTAAGT[A/G]TTTTGCAGGTAGGTC | 51666 |
rs763227024 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95511553 | TGTAATCACAGCTAC[C/T]TGGGAGGCTGAGGCA | 51666 |
rs763254650 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95537232 | GAGTGAGCTGCATTA[A/G]TCCTTCACTTCCATT | 51666 |
rs763271524 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95526037 | AAACGGATTTTTTTT[A/T]AAGCTAACAAAATGC | 51666 |
rs763293924 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95490909 | TAGCTACAAGTGATA[G/T]CAGTTTGGAGGTAAA | 51666 |
rs763298394 | snp | A/C | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472929 | AAAATCAAACTGTCT[A/C]AGTACAAGGAAACCA | 51666 |
rs763421536 | snp | A/G | 6.59478e-05 | 0.00574191 | missense | ASB4 | GRCh38.p7 | 7:95496004 | GACACACAGCTTTGC[A/G]CTTTTGTACAACTCC | 51666 |
rs763421697 | snp | C/T | 1.64931e-05 | 0.00287163 | synonymous-codon, intron-variant | ASB4 | GRCh38.p7 | 7:95537699 | AGCAATTCCTTTGCT[C/T]TCCCTCCCATTGTCA | 51666 |
rs763451826 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95491470 | ATAGTAAAAGGGCAG[A/C]CTGAAGTCTGCAGAG | 51666 |
rs763533637 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95496921 | AAAAAAGAACGCCGA[A/G]AGGAAGAGGGGTCTA | 51666 |
rs763554323 | in-del | -/TAAAT | | | | | GRCh38.p7 | 7:95464411 | ACCTAGATTGATAAA[-/TAAAT]TAAAGTGACAATTAG | 51666 |
rs763618059 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95525564 | AGGTCAAAGATCAAT[C/T]GTAAATGTCCAAGTA | 51666 |
rs763666771 | snp | C/T | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484488 | GTTGATTACATGAGT[C/T]TGTTCACTAAAAATT | 51666 |
rs763668919 | snp | C/T | | | | | GRCh38.p7 | 7:95467355 | CCTTATTCCTTTTCA[C/T]GAAAATAGATGAATT | 51666 |
rs763779794 | in-del | -/TC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515221 | TTCTTTCTTTCTTTC[-/TC]TTTCTTTCTTTTTCT | 51666 |
rs763798848 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95498953 | AAAAATCAATTGGCA[A/G]TATATGTATGGGTTT | 51666 |
rs763813324 | snp | A/G | 3.31422e-05 | 0.00407063 | missense | ASB4 | GRCh38.p7 | 7:95527843 | TGAAGACCAACAACC[A/G]AGATGAGGAGACGCC | 51666 |
rs763815042 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95511682 | AAAAAAAATAAATAA[A/G]TAAAAATAACAACAG | 51666 |
rs763887643 | in-del | -/TTCCCTTC | 5.20494e-05 | 0.00510118 | intron-variant | ASB4 | GRCh38.p7 | 7:95536555 | TGACTTGGAGGTAAA[-/TTCCCTTC]TAATCGATTCCCTTC | 51666 |
rs763911902 | snp | A/G | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473422 | GGAGAGCAGCTGCCT[A/G]GCTGTGAGAGCCACA | 51666 |
rs763921518 | snp | A/T | | | | | GRCh38.p7 | 7:95460370 | ACAGGAAAATATGGG[A/T]AAGTTTGGAACTTCT | 51666 |
rs763927661 | in-del | -/T | 0.377608 | 0.224907 | intron-variant | ASB4 | GRCh38.p7 | 7:95495738 | AAACTTTCCTTTTCC[-/T]TTTTTTTTTTTTTTT | 51666 |
rs763947521 | snp | G/T | 1.66012e-05 | 0.00288103 | missense, intron-variant | ASB4 | GRCh38.p7 | 7:95537738 | GTACTTGCTTTTAGA[G/T]CCAGAGGGAATTATT | 51666 |
rs763960769 | snp | A/G | 1.66535e-05 | 0.00288556 | splice-donor-variant | ASB4 | GRCh38.p7 | 7:95486159 | CATCTTATAAACAAG[A/G]TAAAAACATATAGGT | 51666 |
rs763989457 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95537482 | GGAAGCTGCCATTAC[A/G]TATAGAGGTTAGTTG | 51666 |
rs763992474 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95504684 | ATAAAAAATTGAAAC[A/C]CAAAATCCCTTGACA | 51666 |
rs764004715 | in-del | -/A | | | intron-variant | ASB4 | GRCh38.p7 | 7:95523595 | ATCACAGAGAGAGAT[-/A]AAAATATAACTTTTG | 51666 |
rs764064204 | in-del | -/AAT | | | | | GRCh38.p7 | 7:95465118 | GATGAAATAGTTGAA[-/AAT]AACACACTTGGCCCT | 51666 |
rs764111578 | snp | A/G | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538513 | AGTGATGGGGCAAGA[A/G]TACAGGTGCAGACTC | 51666 |
rs764148676 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95532287 | TTCTTCCAAATACAA[A/G]GCCAATTTGTAGAGG | 51666 |
rs764154588 | snp | C/T | | | | | GRCh38.p7 | 7:95466954 | ATGACACGTGGGGAT[C/T]ATGGGAGCTACAATT | 51666 |
rs764158961 | snp | A/G | | | | | GRCh38.p7 | 7:95481897 | GAATGGAGAGTTTTC[A/G]TTTTTAAGAGCTGAG | 51666 |
rs764178118 | snp | A/G | 4.9476e-05 | 0.00497348 | missense | ASB4 | GRCh38.p7 | 7:95528151 | ATGCTGGAAGCTGGC[A/G]CCGAAGCCAATCTCA | 51666 |
rs764262744 | snp | A/T | | | | | GRCh38.p7 | 7:95480865 | TACAGTGTCTGGCTC[A/T]TAGTAAGTTCCCAAA | 51666 |
rs764288222 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95526977 | AGTCTGTTAAATAAA[C/T]GGGTTGGATTAAGTA | 51666 |
rs764448498 | snp | C/T | | | | | GRCh38.p7 | 7:95483416 | GAAAGCCTGAACTCT[C/T]AAACACAGAGAATTT | 51666 |
rs764490291 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95534891 | TTCTCGTTAAGAGTG[C/T]ATAATAGCCTCTTCT | 51666 |
rs764491614 | snp | C/T | | | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471216 | AGGAAAAAAGACGCA[C/T]GTCCCCTTCAAATGA | 51666 |
rs764495657 | snp | C/T | 1.69015e-05 | 0.00290696 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95536544 | TATCCCCGATGATGA[C/T]TTGGAGGTAAATAAT | 51666 |
rs764509855 | in-del | -/GC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95502389 | AATAGGTACCAGCCT[-/GC]GCGGGGGGGGGGCAA | 51666 |
rs764526399 | snp | C/G | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472808 | GCAACACAGGTCTAT[C/G]TATAACATTTCAGCT | 51666 |
rs764528090 | snp | C/T | 1.65056e-05 | 0.00287272 | missense | ASB4 | GRCh38.p7 | 7:95495791 | ATAAATTGAAGTCTT[C/T]CTGGGCCACAGGCCT | 51666 |
rs764538985 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95501479 | CTCTTACCACCTCAC[C/T]GCATTCCATCTTTTC | 51666 |
rs764571947 | snp | A/C | 1.658e-05 | 0.00287919 | missense | ASB4 | GRCh38.p7 | 7:95536470 | TCTTGTCCTAAAGCA[A/C]TTGAAGTTGTAGTCA | 51666 |
rs764581157 | snp | A/C | 1.64904e-05 | 0.00287139 | missense | ASB4 | GRCh38.p7 | 7:95495898 | CCCAATGGGAAAACC[A/C]CTCTTCACGTGGCTT | 51666 |
rs764589820 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95533745 | CTTAAATCTCTGAAA[G/T]GGGGATGAATATAGG | 51666 |
rs764628233 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95488608 | CTGTGTGGCCTTAAA[A/T]GGTATGTGGCTGGAT | 51666 |
rs764652033 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95526114 | GTAAACTACAGAAAA[A/C]TTTTCCTTCAGAAAA | 51666 |
rs764653264 | in-del | -/GGCCAGGG | | | intron-variant | ASB4 | GRCh38.p7 | 7:95534075 | ATGGCTGGGCGCGGT[-/GGCCAGGG]GGCTTACACCTGTAA | 51666 |
rs764747771 | snp | C/T | 1.76456e-05 | 0.00297026 | intron-variant | ASB4 | GRCh38.p7 | 7:95536560 | TTGGAGGTAAATAAT[C/T]GATTCCCTTCTAATA | 51666 |
rs764749735 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95489396 | GATTTAGAAGCCAGC[C/T]TCCAGAGTTCATGTT | 51666 |
rs764751050 | snp | C/T | | | | | GRCh38.p7 | 7:95476381 | CTTGCAGGTGACTGA[C/T]ATTCTTTTTTATATT | 51666 |
rs764753113 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95489526 | AATCTGCAGATGAAA[C/T]CATGTTTTATTAATT | 51666 |
rs764772623 | snp | A/G/T | 4.96342e-05 | 0.00498147 | missense | ASB4 | GRCh38.p7 | 7:95536504 | CCTATGAACACATCA[A/G/T]ATGGAACACAAAGTG | 51666 |
rs764793377 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95532322 | ATTTCACTGAAAGCC[A/G]ATGTGTAAATTACAT | 51666 |
rs764823539 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95518509 | CTTCTGTTGCTCTAA[A/G]CCACTGAAATATGAG | 51666 |
rs764846555 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95533388 | CACTCTTCGTGCTGT[A/G]ACACCAAGGGTCTTA | 51666 |
rs764853560 | snp | A/G | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539807 | GCTCCAGTGATGGGT[A/G]CACTAAAATCTCAAA | 51666 |
rs764859532 | in-del | -/A | | | downstream-variant-500B | LOC107986823 | GRCh38.p7 | 7:95475043 | CTGTAGAGCCTATAG[-/A]ACAAGCTGTTTTTTA | 51666 |
rs764921333 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95519151 | CACAAGAGAATATAT[C/T]TGCCATAGAATGTAG | 51666 |
rs764930042 | snp | A/G | | | downstream-variant-500B | LOC107986823 | GRCh38.p7 | 7:95474663 | AGTAGCTGAAACTAC[A/G]GGCACATGCCACCAT | 51666 |
rs764957710 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95507214 | TGACATAGTCTCTTA[C/T]GAATTTTTTTTTCCT | 51666 |
rs764986532 | snp | G/T | | | | | GRCh38.p7 | 7:95461430 | ACTTGCATGGGACCT[G/T]TAGCCCCTTTGTTTT | 51666 |
rs765011498 | snp | G/T | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538555 | TTATCTTTCAAAGTT[G/T]TGTTTCTGACATGAA | 51666 |
rs765042692 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95506248 | CTCAGTGGGTATTTT[A/G]TCAATGTTATTTTCT | 51666 |
rs765049768 | snp | C/T | | | | | GRCh38.p7 | 7:95466663 | GTATTAGTCCATTTT[C/T]ATACTGCTATGAAGA | 51666 |
rs765064843 | snp | C/G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95526430 | TCTCTGCTGTGCTGC[C/G/T]GGTTGCAACTTTGCA | 51666 |
rs765187745 | snp | G/T | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539466 | CTATATCATGGAATA[G/T]AATGCTGAATTTGTA | 51666 |
rs765194679 | in-del | -/GTGT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95493366 | AAGAGATGAAAGTGT[-/GTGT]GTGTGTGTGTGTGTG | 51666 |
rs765262960 | snp | C/T | | | | | GRCh38.p7 | 7:95483070 | GACGGGCTGCAGCGT[C/T]TGAGAACATCAAAAC | 51666 |
rs765276802 | snp | A/C | 1.64993e-05 | 0.00287218 | missense | ASB4 | GRCh38.p7 | 7:95528250 | CCTGAGATCTGCTAC[A/C]AGCTCCTGTTGAACC | 51666 |
rs765289269 | in-del | -/TCTTTCTCTT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515161 | TTCTTTCTTTCTTTC[-/TCTTTCTCTT]TCTTTCTCTTTCTTT | 51666 |
rs765318890 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95495188 | TCGTCTTTGGAAAGC[A/G]ATATTGCATAAATCA | 51666 |
rs765331765 | snp | A/T | 1.64773e-05 | 0.00287026 | missense | ASB4 | GRCh38.p7 | 7:95486072 | ACTTCGGAAAATTGA[A/T]GGCTATTTTGATCCA | 51666 |
rs765347992 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95511371 | CAGAATTCTGGCAGC[C/T]CTCAGCAACACTCTT | 51666 |
rs765392360 | snp | A/G | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95470109 | GATACTGTGCATAGA[A/G]CCTCTTCCTGGAAAA | 51666 |
rs765419369 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95488767 | AGTGTGCAGCTTGAT[C/T]ACTTTTCACAAAATA | 51666 |
rs765506289 | snp | C/T | 1.64917e-05 | 0.00287151 | missense | ASB4 | GRCh38.p7 | 7:95528167 | CCGAAGCCAATCTCA[C/T]GGATATCAACGGCTG | 51666 |
rs765536207 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95531697 | GTGAGTCCCTGCCCA[A/G]AGACTAAATGTTGAC | 51666 |
rs765595046 | snp | G/T | 1.64909e-05 | 0.00287144 | missense | ASB4 | GRCh38.p7 | 7:95495910 | ACCCCTCTTCACGTG[G/T]CTTGTGAAATGGCCA | 51666 |
rs765619625 | snp | G/T | 3.2969e-05 | 0.00405998 | missense | ASB4 | GRCh38.p7 | 7:95495997 | TTAAGTGGACACACA[G/T]CTTTGCACTTTTGTA | 51666 |
rs765649661 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95535027 | GGTTGGCCTCTTTAC[C/T]GTCAACACACACAGA | 51666 |
rs765702937 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95535798 | CAATAAGTGTGGTTT[A/G]GTACATGACACCAGC | 51666 |
rs765713522 | snp | A/G | | | | | GRCh38.p7 | 7:95478063 | CTTCTGACAACTGTG[A/G]GTGTAAAAAGAACGT | 51666 |
rs765722378 | snp | A/C | | | | | GRCh38.p7 | 7:95479314 | TCCACTGATATGAAC[A/C]ACAGTAATAATATGT | 51666 |
rs765827426 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95523674 | TAATTCTATTTTGGG[A/G]GAATTTATTCCAAGG | 51666 |
rs765853822 | snp | C/G/T | 3.30067e-05 | 0.00406232 | synonymous-codon, intron-variant | ASB4 | GRCh38.p7 | 7:95537627 | TAACTCTCCAAGGAC[C/G/T]CTCATGCACTTATCG | 51666 |
rs765874502 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95521022 | AATTTTGTGGGGAAA[A/C]ATGTTTGAATTGCAT | 51666 |
rs765905478 | snp | A/G | 1.64906e-05 | 0.00287142 | missense | ASB4 | GRCh38.p7 | 7:95496012 | GCTTTGCACTTTTGT[A/G]CAACTCCAAGTTCCA | 51666 |
rs765977714 | in-del | -/TT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515159 | TTTTTCTTTCTTTCT[-/TT]CTCTTTCTCTTTCTT | 51666 |
rs765998348 | snp | C/T | | | | | GRCh38.p7 | 7:95476001 | TTTCAAATACCATTT[C/T]CTCTGTGAAATCTTT | 51666 |
rs765999291 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95521861 | AAGCAATGATAAGCA[A/T]CAATTTTAGAACAGT | 51666 |
rs766063618 | snp | A/G | | | | | GRCh38.p7 | 7:95464925 | TGTTTATTGACAACA[A/G]TAAGTTATTTTTCTC | 51666 |
rs766078059 | snp | C/T | 6.59489e-05 | 0.00574196 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95528126 | CTGTGACCACGTGCT[C/T]ATGCACATGATGCTG | 51666 |
rs766087379 | snp | G/T | 0.000163575 | 0.00904218 | intron-variant | ASB4 | GRCh38.p7 | 7:95536577 | ATTCCCTTCTAATAG[G/T]TTTCACTATCAAGTA | 51666 |
rs766105787 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95489086 | ATTTTATCCCTAAAT[A/G]TAGTCCATCTAAGCC | 51666 |
rs766121186 | snp | A/G | | | | | GRCh38.p7 | 7:95462778 | GATTATTCTGGTTTT[A/G]CATATATAAAGACAT | 51666 |
rs766153453 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95527310 | GGGATGGGAAGTTTC[C/T]ATACCACTAAAGTTT | 51666 |
rs766215291 | snp | A/C | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539795 | ACAGTGTACACTGCT[A/C]CAGTGATGGGTGCAC | 51666 |
rs766285736 | in-del | -/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513982 | ATCACCCTCACAACT[-/C]CTGGACCTCCACAAT | 51666 |
rs766317704 | snp | C/T | 1.90416e-05 | 0.00308552 | utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485930 | TTGCTCGGTGCTGTT[C/T]TCTCGATAAATCACA | 51666 |
rs766371560 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95516106 | AGTCCTTATCACTTT[A/G]TCCAAACTTGTATCT | 51666 |
rs766378652 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95517239 | AGTGGAGCCATCATA[C/G]CTCACTGTAACCTCA | 51666 |
rs766403817 | in-del | -/TT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515190 | TTCTTTCTTTCTTTC[-/TT]TCTTTCTTTCTTTCT | 51666 |
rs766444091 | snp | C/T | 3.98971e-05 | 0.0044662 | intron-variant, utr-variant-3-prime | ASB4 | GRCh38.p7 | 7:95528386 | AGTAACTCAAGCTTG[C/T]TTGAGGCTTGAGTCC | 51666 |
rs766481963 | snp | G/T | | | intron-variant, nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471575 | ACACTGTCAGTGTAC[G/T]TCTGTGACAGTATGT | 51666 |
rs766491257 | in-del | -/A | 1.6611e-05 | 0.00288188 | frameshift-variant | ASB4 | GRCh38.p7 | 7:95536527 | CAAAGTGGAGAAGAG[-/A]CTATCCCCGATGATG | 51666 |
rs766500437 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95531457 | AGAGAAACATACTCT[A/G]TCACTTTATCCATGA | 51666 |
rs766535370 | snp | A/G | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472342 | GAATGATCTGTTGCC[A/G]CCATCTTGAAAATCT | 51666 |
rs766559083 | snp | A/C | 1.6477e-05 | 0.00287024 | missense | ASB4 | GRCh38.p7 | 7:95486077 | GGAAAATTGAAGGCT[A/C]TTTTGATCCAAAGGC | 51666 |
rs766588725 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95504206 | TGAAGCAAATCCTGA[C/G]AGTAGGAGGAAAATT | 51666 |
rs766790224 | snp | C/T | 3.30028e-05 | 0.00406205 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95528259 | TGCTACCAGCTCCTG[C/T]TGAACCATGGGGCTG | 51666 |
rs766798932 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95523784 | AGTAGGGTAAACTTA[C/T]TCTAAGGAGTATGTA | 51666 |
rs766837992 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95499054 | TGATTGCCACAGGTT[C/T]GTATCAAGTCTTGAA | 51666 |
rs766851636 | snp | C/T | | | | | GRCh38.p7 | 7:95467390 | TTTGTGAAAGCTCAG[C/T]AGTGGATGGGTGGGG | 51666 |
rs766853284 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95524443 | TTTTCTGGGGCTAAG[A/G]GTGTCTAATTTCTTG | 51666 |
rs766862142 | snp | A/G | | | | | GRCh38.p7 | 7:95468622 | TAAGTCATATCTGTC[A/G]TTTTAAGTGCTCATT | 51666 |
rs766884841 | snp | C/G | | | | | GRCh38.p7 | 7:95467313 | CACAGCTTGTGTGAC[C/G]CTGAGAAAGTTACTT | 51666 |
rs766899389 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95522129 | CAGTAACACAACAGA[A/G]TTCTCTCTTTTATAT | 51666 |
rs766977688 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95512307 | TCTTTGAATCTTAGC[C/T]CTCACCTACCAAATG | 51666 |
rs767015489 | snp | C/T | 1.65203e-05 | 0.002874 | missense | ASB4 | GRCh38.p7 | 7:95496030 | ACTCCAAGTTCCATT[C/T]TCTGTGCCAAGCAAT | 51666 |
rs767024486 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95509000 | TGTGGGTTGGAGTCA[C/T]CAAGTCAGAGTAGGA | 51666 |
rs767043809 | snp | A/T | 1.65866e-05 | 0.00287976 | missense | ASB4 | GRCh38.p7 | 7:95527840 | ACATGAAGACCAACA[A/T]CCAAGATGAGGAGAC | 51666 |
rs767068427 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95523582 | ATTAGTCTTATGCAT[A/C]ACAGAGAGAGATAAA | 51666 |
rs767150902 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95510168 | TATATTAGAAGTGTG[C/T]TTAATGAAAAGATAT | 51666 |
rs767152808 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513671 | CCAGCCAAGTTGTTA[A/C]ATAAAATTAACCATT | 51666 |
rs767206088 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95496804 | AGTGACTTGTGATTA[C/T]GCCACTGCACTCCAG | 51666 |
rs767213579 | in-del | -/TG | | | | | GRCh38.p7 | 7:95467536 | AACATTGTAAAATTG[-/TG]TGTGTGTGTGTGTGT | 51666 |
rs767242589 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485891 | ATTAGCCGACAGTTT[A/G]TGGACTCTCCAGCAT | 51666 |
rs767259672 | in-del | -/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95521650 | GAATAGCTAAACTGT[-/G]GTTTATACAAGGTAA | 51666 |
rs767371772 | snp | C/T | 1.64963e-05 | 0.00287192 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95528225 | CACCTCCGTGCGCCC[C/T]GCTGCCCAGCCTGAG | 51666 |
rs767418822 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95534235 | TGTAATCCCAGCTAC[C/T]TGGGAGGTGAGGCAG | 51666 |
rs767456009 | in-del | -/TC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515200 | CTTTCTTTCTTTCTT[-/TC]TTTCTTTCTTTCTTT | 51666 |
rs767514244 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95529046 | GACCAGTTGCTACCA[C/G]TATTGATATGACTAA | 51666 |
rs767514315 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95505821 | AAACTGTCTTATTTC[A/G]TTCTTTTGCTTAATT | 51666 |
rs767526301 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95504521 | TGTAATAGCATAAAT[A/C]TGACCATGTTAGACA | 51666 |
rs767554496 | snp | A/G | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473183 | TTCTCACCTCTATCC[A/G]TCAGAGGAGTCAGAG | 51666 |
rs767554812 | in-del | -/CTT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95512036 | CTGCCACTCCCTCAG[-/CTT]CTTCTATAACTGCCT | 51666 |
rs767565402 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95492318 | GGAAAAAAATTCAAC[C/T]AGCAAATGCATTTCC | 51666 |
rs767602746 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95500894 | TCTTCGCTTTTGCAG[A/C]CTCCCACTTAGGAAG | 51666 |
rs767654732 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95491247 | AGGGGAAATAATCTC[C/T]ATTTTTCTTTTCTTC | 51666 |
rs767659880 | snp | A/C | | | | | GRCh38.p7 | 7:95479677 | AAACAAAACTATCAT[A/C]AATTATAAGCCATTT | 51666 |
rs767660330 | snp | C/T | | | | | GRCh38.p7 | 7:95459950 | CCCTTATGTTGTTCT[C/T]GTGATGGTGAGTTCT | 51666 |
rs767706920 | snp | C/T | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538493 | CACAGCTAACTGCAA[C/T]ATAAAGTGATGGGGC | 51666 |
rs767916695 | in-del | -/A | 1.84116e-05 | 0.00303405 | intron-variant | ASB4 | GRCh38.p7 | 7:95495723 | CTAGGTCAAGAAGTT[-/A]AAACTTTCCTTTTCC | 51666 |
rs767960939 | snp | A/T | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469717 | CAACAGTAATGCATT[A/T]AATTGTTGGTTCATT | 51666 |
rs767977243 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95532395 | AGGGTACAAAAGGAC[A/T]TTTGATTTTTTTTTC | 51666 |
rs768023810 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95493553 | TGGACAGAGAGACAA[C/T]AGCTTATTTTGATTT | 51666 |
rs768038032 | snp | C/T | 0.000115465 | 0.00759731 | missense | ASB4 | GRCh38.p7 | 7:95528011 | AGCAGGAGTACAGCA[C/T]GGAGCACCACCTGGT | 51666 |
rs768220115 | snp | A/T | | | | | GRCh38.p7 | 7:95481629 | TCAAATTCATGTTTA[A/T]ATGCCATGATAAACC | 51666 |
rs768226765 | in-del | -/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95486837 | CAAAAATTAGACCAA[-/T]TTTTTTTTTACCAAG | 51666 |
rs768237505 | snp | A/G | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538156 | AAATGGCCATATAGC[A/G]GGCTTTGCAATTGGC | 51666 |
rs768244466 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95499925 | GTCGCCTGGGCTGGA[A/G]TGCAGTGGTGCGATC | 51666 |
rs768306865 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95523311 | TCAAACTGGTTACAA[C/T]GTTTATAGCAATTAT | 51666 |
rs768376306 | snp | C/T | | | | | GRCh38.p7 | 7:95468427 | AGTATGTAAAACCAC[C/T]GAACAGAAGACCATG | 51666 |
rs768418557 | snp | C/T | 1.73872e-05 | 0.00294844 | intron-variant | ASB4 | GRCh38.p7 | 7:95536431 | AACTCTGTGCTTCCT[C/T]TGCAGGTGATACAGG | 51666 |
rs768429381 | snp | C/T | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469399 | TGAATGAAAGAATAA[C/T]ATTACATCATCACCA | 51666 |
rs768437307 | snp | C/T | 0.00155159 | 0.0278098 | intron-variant | ASB4 | GRCh38.p7 | 7:95495740 | AACTTTCCTTTTCCT[C/T]TTTTTTTTTTTTTTC | 51666 |
rs768463268 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95533966 | TGTCACTGAACTTCA[C/T]GGCTTCTGCCAGCAC | 51666 |
rs768489221 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95499670 | AAGTGAACATAAGAA[G/T]AGCATGATTGCTGGA | 51666 |
rs768490367 | snp | G/T | 1.64909e-05 | 0.00287144 | missense | ASB4 | GRCh38.p7 | 7:95495845 | ATGTGGAATGTCTTC[G/T]GGTGCTACTGGACCA | 51666 |
rs768511774 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95533092 | GGAGGAATTGACTTA[A/G]CTTGCTCAACCTTGG | 51666 |
rs768516202 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95521722 | CTATTCAAAGACATG[C/T]TGTGATGGATAAAAA | 51666 |
rs768527508 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95487852 | CATTCTTATGTATGC[C/T]AAGTGGATGCTTGCA | 51666 |
rs768530329 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95500693 | GTTAAAAATGAGGCT[A/G]TATCCCATATTCTCT | 51666 |
rs768598230 | snp | A/T | | | | | GRCh38.p7 | 7:95462556 | ATTAAAACAAGAGAC[A/T]TCTACATGGGCCTAG | 51666 |
rs768634678 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95520466 | AGGCTTGGCTAAAAA[C/T]GTGCCCATCAAAAGT | 51666 |
rs768730270 | snp | A/G | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539290 | TAATGTTAACTGGCA[A/G]TCACCTAACTGGTTA | 51666 |
rs768850292 | snp | A/T | 2.10937e-05 | 0.00324752 | intron-variant | ASB4 | GRCh38.p7 | 7:95527770 | CTTAGGAATAATGAC[A/T]AAACATGTTTAAATA | 51666 |
rs768863503 | snp | A/G | 1.6486e-05 | 0.00287102 | missense, intron-variant | ASB4 | GRCh38.p7 | 7:95537659 | GATGTGCCATTAGAA[A/G]AACATTACACAACAG | 51666 |
rs768869913 | in-del | -/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95505688 | TCCTCTATCCGTGTC[-/C]CCCCCCCCCCAAATA | 51666 |
rs768876128 | snp | C/T | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95483733 | GGGCAGGGATTTCTG[C/T]GTTTGTTCACTGCTG | 51666 |
rs768880722 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95508177 | GATAATTTTTGGTGT[A/G]AGGATTCTGAGAAGT | 51666 |
rs768912622 | snp | A/T | | | downstream-variant-500B, intron-variant | ASB4 | GRCh38.p7 | 7:95540668 | TGAAGAAAAAAACAA[A/T]CTCTCTTCTGAAACT | 51666 |
rs768934179 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95509352 | GGCCAGAGTTAAGCA[G/T]CCCACATCCGTTGTT | 51666 |
rs768976493 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95502879 | CTATTTGCCCTCAGA[A/G]AGTCATTTATATTAC | 51666 |
rs769020373 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95529843 | ATTACTCACATTTAA[A/G]AGGTGACTAAGCTAA | 51666 |
rs769050117 | snp | C/T | 1.69132e-05 | 0.00290797 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95485980 | AGGAAGGATGGACGG[C/T]ACCACTGCCCCTGTC | 51666 |
rs769058541 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95496207 | AATACATAGTTCTGT[A/T]GATTCAGGTAATTCA | 51666 |
rs769212820 | snp | C/G | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472693 | GACAGGCTCTGAATT[C/G]CACAGCAGGGTTAAC | 51666 |
rs769255904 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95504016 | GTATTAGTAAAATAA[A/T]GTTCATCAGTTGAGA | 51666 |
rs769262085 | in-del | -/CGAAGT | 8.24457e-05 | 0.00641997 | cds-indel | ASB4 | GRCh38.p7 | 7:95528054 | GCTTGACTACAAAGC[-/CGAAGT]CAATGCCCGAGATGA | 51666 |
rs769268446 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95501238 | AAAATTTGTTACTGC[A/C]GGAAAGCCATAAAAA | 51666 |
rs769286014 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95509589 | TAATATCTTTGTGCG[C/T]CAGTCCTCCTAGCTA | 51666 |
rs769323349 | snp | A/G | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469455 | AATGATCTGTCTCCT[A/G]CAAGTGTGGCCTGTG | 51666 |
rs769480417 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95506046 | CTACAGGCACATGGG[C/T]CGTGCCTGGCTAATT | 51666 |
rs769481837 | snp | A/G | 1.66269e-05 | 0.00288326 | missense | ASB4 | GRCh38.p7 | 7:95486000 | CTGCCCCTGTCACTA[A/G]ATCTGGAGCTGCCAA | 51666 |
rs769492220 | in-del | -/TC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515340 | CTTCCTTCCTTTCTT[-/TC]TTTCTTTCTTTTTCT | 51666 |
rs769514212 | snp | G/T | 1.64874e-05 | 0.00287113 | missense | ASB4 | GRCh38.p7 | 7:95528112 | AAGGCAGCCTGGAAC[G/T]GTGACCACGTGCTCA | 51666 |
rs769547361 | snp | C/G | | | | | GRCh38.p7 | 7:95475842 | CCCCCATCTCTAATC[C/G]TTGCCATGAGCTGGC | 51666 |
rs769573705 | snp | A/G | 1.64904e-05 | 0.00287139 | missense | ASB4 | GRCh38.p7 | 7:95495863 | TGCTACTGGACCACA[A/G]TGCTACAATCAACTG | 51666 |
rs769587330 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95535347 | TTGTTTAAGTGCAGA[G/T]GCATGCCTCTCTTCT | 51666 |
rs769610355 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95523239 | CATTCTGGTACAAAG[A/G]AAAAGGCAAGGGAAA | 51666 |
rs769642093 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95521781 | GTAGTTTTTTAAAAC[A/G]CAAAATAATAGTATA | 51666 |
rs769671951 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95509465 | ACTAAGCACTTAGCA[A/G]TAGCTTCTGAATAAA | 51666 |
rs769769709 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95508441 | TTGTTAGAGAGGAAA[A/T]ATTATATTTTCTATA | 51666 |
rs769848762 | snp | C/T | | | | | GRCh38.p7 | 7:95466858 | AAAACTATCAGATAT[C/T]GTGAGACTTATTCAC | 51666 |
rs769862245 | in-del | -/GTGTGTGT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95493362 | AAAAAAGAGATGAAA[-/GTGTGTGT]GTGTGTGTGTGTGTG | 51666 |
rs769935368 | snp | C/G | | | | | GRCh38.p7 | 7:95467540 | ATTGTAAAATTGTGT[C/G]TGTGTGTGTGTGTGT | 51666 |
rs769944862 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95531414 | TCCAGCGAAAAGGAT[A/G]GACAGGGACACAGGG | 51666 |
rs769947845 | snp | A/C | 1.78867e-05 | 0.00299049 | intron-variant, missense | ASB4 | GRCh38.p7 | 7:95528364 | GCAGCCTTGTCTGAA[A/C]TCTCCAAGTAACTCA | 51666 |
rs769948444 | snp | A/T | | | | | GRCh38.p7 | 7:95468580 | AGTAGTAGGAAAAAC[A/T]CTCAAGTTAATGAAG | 51666 |
rs770009151 | snp | A/G | 1.65021e-05 | 0.00287241 | missense | ASB4 | GRCh38.p7 | 7:95527890 | CACTTCGGCCTTTCG[A/G]AGCTGGTGGCCTTCT | 51666 |
rs770020838 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95537389 | TGTTATTTCCCCTCC[A/C]CTTTCCTTGTATACC | 51666 |
rs770027108 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95496483 | TGAATGAGGATGTCA[A/G]AAGTGAATTACTATA | 51666 |
rs770037013 | in-del | -/A | | | | | GRCh38.p7 | 7:95464085 | ATTTTGTAGCTTAGT[-/A]AAAAAAAAAAAATCA | 51666 |
rs770042109 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95517036 | TTTCCATGTCCAGAA[A/G]GAAAGTGTTTCCTAT | 51666 |
rs770047821 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95487482 | CAAGTCAGTGGGTAA[C/G]TTATTTGACCCTGAG | 51666 |
rs770080232 | snp | C/G | | | | | GRCh38.p7 | 7:95460949 | CCATGGCTAATAGGG[C/G]CCAATGTGCAGCTCA | 51666 |
rs770085271 | snp | A/C | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95483762 | TGTATCTGCAGTGCC[A/C]AGAATAAGTGTCTGA | 51666 |
rs770087204 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95497848 | TCCATCCATATGGTT[A/G]CATGGACCAATAAAT | 51666 |
rs770098410 | snp | C/T | 3.78179e-05 | 0.00434828 | intron-variant | ASB4 | GRCh38.p7 | 7:95527795 | TAAATAATTGTCTTC[C/T]TCAATTTCCCTTTAT | 51666 |
rs770121440 | snp | A/G | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472159 | TTTGATTATCTACCA[A/G]TGTGTGGGTGTCCCC | 51666 |
rs770121998 | in-del | -/AAAT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95511671 | CGTCTCAAAAAAAAA[-/AAAT]AAATAAATAAATAAA | 51666 |
rs770130688 | snp | A/G | 1.64868e-05 | 0.00287109 | missense, intron-variant | ASB4 | GRCh38.p7 | 7:95537682 | CACAACAGATGCCAT[A/G]GAGCAATTCCTTTGC | 51666 |
rs770153213 | in-del | -/A | 1.64789e-05 | 0.0028704 | frameshift-variant | ASB4 | GRCh38.p7 | 7:95486064 | GTCCAATGACTTCGG[-/A]AAATTGAAGGCTATT | 51666 |
rs770218613 | snp | C/T | 6.62208e-05 | 0.00575378 | synonymous-codon, intron-variant | ASB4 | GRCh38.p7 | 7:95537609 | TCTCTTTACTGTGTG[C/T]TGTAACTCTCCAAGG | 51666 |
rs770222652 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95505273 | AGAGGTAGTGCATTT[A/C]AGATCAATATACAAA | 51666 |
rs770339954 | snp | C/T | 1.64841e-05 | 0.00287085 | missense | ASB4 | GRCh38.p7 | 7:95486114 | ATGTGGACACTGTTT[C/T]TGAAGTCGAAGATGA | 51666 |
rs770346371 | snp | C/G | | | | | GRCh38.p7 | 7:95460740 | TTGCACAAGTAATGA[C/G]GAGCCAAATGTTAAT | 51666 |
rs770395195 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95492018 | TAGCCTGCAAACTGT[C/T]CTCTTGCCATTTCTC | 51666 |
rs770399957 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95537193 | TACTTATTGGCTGTG[C/T]TACTTTTAAAAGTCA | 51666 |
rs770429460 | snp | A/G | 1.66649e-05 | 0.00288655 | intron-variant, missense | ASB4 | GRCh38.p7 | 7:95528325 | CTCTGCCCAGTGGTC[A/G]GCAGGTTGAGGAAGA | 51666 |
rs770461882 | snp | C/T | 3.29875e-05 | 0.00406112 | synonymous-codon, intron-variant | ASB4 | GRCh38.p7 | 7:95537702 | AATTCCTTTGCTTTC[C/T]CTCCCATTGTCATTG | 51666 |
rs770466974 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95500304 | GGAGCCGTGGCTTAT[G/T]CTTGTAATCCCAGAA | 51666 |
rs770471618 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95514531 | AGTTAGAGGAAGAGG[C/T]TGACTGACATGTTCA | 51666 |
rs770478902 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95535484 | TCATGATGAACAAAT[G/T]TAGAAGAGCAGATCT | 51666 |
rs770552325 | snp | C/T | | | | | GRCh38.p7 | 7:95477657 | TAATTAATTATGCAA[C/T]TTTGTGCAAACATGT | 51666 |
rs770571207 | snp | C/T | 1.65089e-05 | 0.00287301 | missense | ASB4 | GRCh38.p7 | 7:95486035 | GTTAAGAGAAATTTC[C/T]TTGAGGCGCTAAAGT | 51666 |
rs770594349 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95502550 | ACTTTAGATGTTATC[G/T]CTGAACTAGGTTATA | 51666 |
rs770606672 | in-del | -/TGG | | | intron-variant | ASB4 | GRCh38.p7 | 7:95534575 | AGCCTGGGAGCCGGT[-/TGG]TGCACTTCCCATTAG | 51666 |
rs770614933 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95523329 | TTATAGCAATTATGA[C/T]AGCATAAGCTTATAT | 51666 |
rs770655142 | snp | A/G/T | 4.02812e-05 | 0.00448765 | intron-variant, utr-variant-3-prime | ASB4 | GRCh38.p7 | 7:95528391 | CTCAAGCTTGCTTGA[A/G/T]GCTTGAGTCCTGGGC | 51666 |
rs770656249 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95517991 | AGCAATGTTCTACTG[C/T]TGGGTGTATGATCAA | 51666 |
rs770731569 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95509691 | GAAATTGATGTTGCC[A/G]GTATACATGCATATG | 51666 |
rs770732908 | snp | A/G | | | | | GRCh38.p7 | 7:95478878 | TAATTACAATTGAGA[A/G]TGAATACGCCGAACT | 51666 |
rs770739646 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95524117 | TACCCAGTGACCCAG[A/C]AATTCCACTCATAGA | 51666 |
rs770773904 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95490516 | GACACAGGCAGAGCA[A/G]ATGTCTGCTAATCCA | 51666 |
rs770776860 | in-del | -/C | | | | | GRCh38.p7 | 7:95463681 | GCCTCTCCAGCCATG[-/C]CTTCCTGCGCAGCCT | 51666 |
rs770804094 | snp | A/C | 1.64974e-05 | 0.00287201 | missense | ASB4 | GRCh38.p7 | 7:95528220 | AAGGTCACCTCCGTG[A/C]GCCCTGCTGCCCAGC | 51666 |
rs770832787 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95496561 | TTTTAAGAATGAAAA[A/G]GACGGCCAGGTGCTG | 51666 |
rs770873239 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95530327 | AAAATTAGCTGGGTG[A/T]TGTGGCGTGCGCCTG | 51666 |
rs770959162 | snp | C/G | 3.31846e-05 | 0.00407323 | missense | ASB4 | GRCh38.p7 | 7:95536525 | ACACAAAGTGGAGAA[C/G]AGCTATCCCCGATGA | 51666 |
rs770993036 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95495361 | ATTCAAGACAAACTC[G/T]CAATGATTGAAAGTT | 51666 |
rs771031112 | snp | A/G | 1.68618e-05 | 0.00290356 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95536445 | TCTGCAGGTGATACA[A/G]GCCTGCCATTCTTGT | 51666 |
rs771099175 | in-del | -/AAAAA | | | intron-variant | ASB4 | GRCh38.p7 | 7:95500569 | AGCAAGATCTGTCTC[-/AAAAA]AAAAAAAAAAAAAAA | 51666 |
rs771135306 | snp | C/T | 4.94425e-05 | 0.0049718 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95486061 | AAAGTCCAATGACTT[C/T]GGAAAATTGAAGGCT | 51666 |
rs771150358 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95531543 | GAAGTGGTTAGCACG[A/G]TGCCATGGGCATGGT | 51666 |
rs771160477 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95533300 | ATGATATTCTGATCT[C/T]TGATTGTCATCTTCA | 51666 |
rs771184275 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95518385 | CTCAGGTAGAGATGG[C/T]GAAGCCATAAGACCA | 51666 |
rs771184533 | in-del | -/GGAAGCTGGT | | | | | GRCh38.p7 | 7:95461773 | CCACGTGTCATGGAA[-/GGAAGCTGGT]GGGAGGTAATTGAAT | 51666 |
rs771227017 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95506777 | TTTGTACTGAGTCCA[G/T]TCAATTCCAAACTGC | 51666 |
rs771229416 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95505620 | AGCAATAGAAGCAGC[C/T]TTATGAGAATCTATT | 51666 |
rs771279008 | snp | A/G | | | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95474229 | TGAACATTCAGTTTA[A/G]TAATTGTCTCTGCCA | 51666 |
rs771285372 | snp | C/T | 1.64993e-05 | 0.00287218 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95527916 | CTTCTACGTGGAACA[C/T]GGGGCCATAGTGGAC | 51666 |
rs771303140 | snp | A/G | | | | | GRCh38.p7 | 7:95482937 | GGTTAGCGGCTCAGC[A/G]TTAGAGAGAATGTAG | 51666 |
rs771313925 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95492207 | TTTATGATTACAGGA[C/G]ATGCAGAAGAAACTG | 51666 |
rs771336747 | snp | G/T | 1.64977e-05 | 0.00287203 | missense | ASB4 | GRCh38.p7 | 7:95527987 | CCTACTGGGCCCTCC[G/T]CTTTAAGGAGCAGGA | 51666 |
rs771373292 | snp | A/G | 1.73117e-05 | 0.00294203 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95537802 | TAGGTATTTAAGTGG[A/G]CTTGCTGGGTAGACA | 51666 |
rs771449533 | in-del | -/T | | | | | GRCh38.p7 | 7:95462674 | ACAAATCACGCTTAC[-/T]GATAATTATGAAATT | 51666 |
rs771454307 | snp | C/T | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538855 | GTAGCAGACTGACAT[C/T]TCATAGCATTGTAGC | 51666 |
rs771500449 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95536961 | GAGTTTTAAAAACCC[C/T]GTCTTGGGTCCTACA | 51666 |
rs771510784 | snp | A/T | 1.6498e-05 | 0.00287206 | missense | ASB4 | GRCh38.p7 | 7:95527932 | GGGGCCATAGTGGAC[A/T]GCGTGAATGCCCACA | 51666 |
rs771512196 | snp | G/T | | | | | GRCh38.p7 | 7:95459669 | TGGGGGAGACATATG[G/T]TGTTTGCTTGGTATT | 51666 |
rs771546799 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95525583 | AATGTCCAAGTACAT[C/T]AAAAAAGGATGTGGT | 51666 |
rs771567397 | snp | C/T | | | | | GRCh38.p7 | 7:95460502 | GAAATAAAGGTGATT[C/T]TTGCTATGCAAAGAG | 51666 |
rs771574376 | snp | A/G | 1.84636e-05 | 0.00303833 | intron-variant | ASB4 | GRCh38.p7 | 7:95495721 | AGCCTAGGTCAAGAA[A/G]TTAAACTTTCCTTTT | 51666 |
rs771619282 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95524238 | ACGGGCAATGCCCAT[A/C]TACAGTTGAATGGAT | 51666 |
rs771627518 | in-del | -/TATGACTTCCTAGGT | | | | | GRCh38.p7 | 7:95480483 | ATAGAAACAGTGGTA[-/TATGACTTCCTAGGT]TAGGTCACAAAAGAT | 51666 |
rs771636512 | in-del | -/TGTGTGTGTA | | | intron-variant | ASB4 | GRCh38.p7 | 7:95493383 | GTGTGTGTGTGTGTG[-/TGTGTGTGTA]TGTGTGTGTGTGTGT | 51666 |
rs771705656 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95486722 | CAAAAGCTGAATTCA[C/G]CAAAACCAAAAAGTT | 51666 |
rs771795818 | snp | A/G | | | | | GRCh38.p7 | 7:95479192 | TATTTGAAACACACA[A/G]CTTATGACCACCAGA | 51666 |
rs771807797 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95525038 | AATTAACCTGGTCAT[A/G]TGACAAGAACCCAGA | 51666 |
rs771886269 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95512834 | TTCTGAGGGCAGATT[C/G]TATCAGTGCGTTAGG | 51666 |
rs771892743 | snp | A/G | 9.4426e-05 | 0.00687052 | intron-variant | ASB4 | GRCh38.p7 | 7:95536412 | ATGTGCATCAAACAG[A/G]TGAAACTCTGTGCTT | 51666 |
rs771920963 | snp | A/C | | | | | GRCh38.p7 | 7:95480175 | CTTATGGTGTGGCTG[A/C]AATCCTAGACCTTAC | 51666 |
rs771937760 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95499696 | CTGGAGGGGGCTGGA[G/T]GGAGGTCACAGGCAA | 51666 |
rs771938368 | snp | C/T | 1.65081e-05 | 0.00287293 | missense | ASB4 | GRCh38.p7 | 7:95486135 | TCGAAGATGAGAATA[C/T]GGTTTTGGCATCTTA | 51666 |
rs772034216 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95490411 | CCCCTTCCCAGGGGA[A/G]CTTTGAGTTATCTGG | 51666 |
rs772127056 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95531708 | CCCAGAGACTAAATG[C/T]TGACTTGTATTCTGA | 51666 |
rs772161575 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95487759 | TTGAGGTGTTTTCAT[A/G]GTGTTAGGACTGTGG | 51666 |
rs772176277 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95532772 | TGGATGGTGAGATGA[A/G]GTGTCTAAATCTCTC | 51666 |
rs772215119 | snp | C/G | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95470712 | GCAGCTGTGGCGACT[C/G]AATCTAAGAAGAAAG | 51666 |
rs772240582 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95507877 | TTAAACAGCTGCTAT[C/T]GGATTTAGTGACATG | 51666 |
rs772291619 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95495096 | CATTTTTATTTTCCT[A/G]CTTTTTTATTTTGCC | 51666 |
rs772300913 | in-del | -/CT | 5.55376e-05 | 0.00526932 | intron-variant | ASB4 | GRCh38.p7 | 7:95536418 | ATCAAACAGATGAAA[-/CT]CTGTGCTTCCTCTGC | 51666 |
rs772302780 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95519960 | TTTGAATATGAACAA[A/T]GTTTCAAAACAGAGT | 51666 |
rs772366404 | snp | A/C | 1.66785e-05 | 0.00288773 | missense | ASB4 | GRCh38.p7 | 7:95536533 | TGGAGAAGAGCTATC[A/C]CCGATGATGACTTGG | 51666 |
rs772375814 | snp | A/C | | | | | GRCh38.p7 | 7:95461122 | ACCCCTCACAGAGTC[A/C]CCACTGGGGCACTGC | 51666 |
rs772386947 | snp | C/T | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539021 | AAAGAAAAATGTAGG[C/T]GATTAAGCTCTGGGC | 51666 |
rs772391061 | snp | C/G | | | | | GRCh38.p7 | 7:95481838 | AGAGCAAAGGACACT[C/G]TTCTGGACATGTAAT | 51666 |
rs772456734 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95514068 | TGGTCCTTTATGGCT[C/T]TCCAGTATTTTCGCT | 51666 |
rs772515263 | snp | C/T | | | | | GRCh38.p7 | 7:95482822 | GTCAGATGGCATGTA[C/T]TCAGCCCTCCTCACA | 51666 |
rs772632934 | snp | A/C | 4.94637e-05 | 0.00497287 | missense | ASB4 | GRCh38.p7 | 7:95528120 | CTGGAACTGTGACCA[A/C]GTGCTCATGCACATG | 51666 |
rs772647047 | snp | A/C | | | | | GRCh38.p7 | 7:95465993 | AGTCTTCCCAATTAG[A/C]ATAGTGCAATTTAAG | 51666 |
rs772686385 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515368 | TTCTTTCTTTCTTTT[C/T]TTTCTTTCTTTTCTT | 51666 |
rs772696309 | in-del | -/TTT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515154 | AATTGTTTTTCTTTC[-/TTT]CTTTCTCTTTCTCTT | 51666 |
rs772706446 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95530946 | GGGTCAAACTTGGAT[A/T]CTGTCACTTACTTAA | 51666 |
rs772719622 | in-del | -/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515173 | TTTCTCTTTCTCTTT[-/C]TTTCTTTCTTTCTTT | 51666 |
rs772744608 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95525500 | AGTATAAAAATAAGG[A/G]ACTCCTATTCAGAAA | 51666 |
rs772748258 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95533520 | ACTTGACCTTCTAAT[G/T]CAATCTGCTGGTATT | 51666 |
rs772757828 | in-del | -/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95486187 | GTGTTATTGTAGAAC[-/T]TGTTAGAAAATGATT | 51666 |
rs772794263 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95514027 | TTTCACTCCAGGTCA[G/T]CTGTGCACTCACATG | 51666 |
rs772798665 | snp | A/C | | | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95470864 | GTTTTATTCAAAATT[A/C]TTTTAAGCCACCACC | 51666 |
rs772838666 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95489368 | GCTTCTCTTACCAAT[C/T]TGGCAGAGAACAGAT | 51666 |
rs772895757 | snp | A/G | | | | | GRCh38.p7 | 7:95477352 | AAGGGTCAACTCTAC[A/G]TCACCTTTTGAATTT | 51666 |
rs772896615 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95488220 | GTGGCGGCCGCCTGT[A/C]GTCCCAGCTACTCCC | 51666 |
rs772942038 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95508487 | TATTATAGGGAATTA[C/T]AGAGAACAGGAAAGT | 51666 |
rs772979304 | snp | A/C | 1.64955e-05 | 0.00287184 | missense | ASB4 | GRCh38.p7 | 7:95528215 | TGCTGAAGGTCACCT[A/C]CGTGCGCCCTGCTGC | 51666 |
rs772995615 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95495204 | ATATTGCATAAATCA[A/G]CAGGCAGGCAAATAA | 51666 |
rs773060502 | snp | C/T | 1.9125e-05 | 0.00309227 | utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485925 | CCTGTTTGCTCGGTG[C/T]TGTTCTCTCGATAAA | 51666 |
rs773116072 | snp | C/T | 1.82988e-05 | 0.00302474 | intron-variant, synonymous-codon | ASB4 | GRCh38.p7 | 7:95528369 | CTTGTCTGAAATCTC[C/T]AAGTAACTCAAGCTT | 51666 |
rs773173916 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95509564 | ATTCATTAAACTTGA[A/G]TAAATAATTTAATAT | 51666 |
rs773274765 | snp | A/C | | | | | GRCh38.p7 | 7:95462948 | AAAATTTAGGTGAGA[A/C]TCCTAAGGGAAACCC | 51666 |
rs773282534 | snp | A/G | 1.66749e-05 | 0.00288741 | intron-variant | ASB4 | GRCh38.p7 | 7:95486161 | TCTTATAAACAAGGT[A/G]AAAACATATAGGTGT | 51666 |
rs773327858 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515898 | CTTGACAAATTCCTT[C/T]TCATACAATTGGCTT | 51666 |
rs773346101 | snp | G/T | 1.72728e-05 | 0.00293872 | intron-variant | ASB4 | GRCh38.p7 | 7:95536433 | CTCTGTGCTTCCTCT[G/T]CAGGTGATACAGGCC | 51666 |
rs773358033 | in-del | -/TGTGTGTGTGTGTGTA | | | intron-variant | ASB4 | GRCh38.p7 | 7:95493377 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGTGTGTA]TGTGTGTGTGTGTGT | 51666 |
rs773387755 | in-del | -/GTT | 1.65666e-05 | 0.00287802 | cds-indel | ASB4 | GRCh38.p7 | 7:95536476 | CCTAAAGCAATTGAA[-/GTT]GTAGTCAATGCCTAT | 51666 |
rs773419918 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95517819 | AAAACAGAGACCACC[C/T]TTTCAAGGAGTTCAA | 51666 |
rs773424431 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485886 | ATAAAATTAGCCGAC[A/C]GTTTGTGGACTCTCC | 51666 |
rs773511769 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95504177 | AAAATGAAAGCTGCC[C/T]GCTTTACTCTGCATG | 51666 |
rs773553402 | snp | A/T | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484979 | ATGTGTGTATATATG[A/T]ATATATGTGTATATA | 51666 |
rs773582169 | in-del | -/CC | 1.95379e-05 | 0.00312547 | intron-variant | ASB4 | GRCh38.p7 | 7:95495737 | TTAAACTTTCCTTTT[-/CC]TTTTTTTTTTTTTTT | 51666 |
rs773587005 | snp | A/C | 3.6708e-05 | 0.004284 | intron-variant | ASB4 | GRCh38.p7 | 7:95527798 | ATAATTGTCTTCCTC[A/C]ATTTCCCTTTATAGG | 51666 |
rs773598978 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95506649 | ATCTTCATTTTTTTA[C/T]GTGAATTTTTATCTT | 51666 |
rs773608502 | snp | A/C | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472831 | TTTCAGCTCTGGTCC[A/C]CCCAGAAACGTGCAC | 51666 |
rs773643647 | snp | A/C | 1.64874e-05 | 0.00287113 | missense | ASB4 | GRCh38.p7 | 7:95496003 | GGACACACAGCTTTG[A/C]ACTTTTGTACAACTC | 51666 |
rs773676846 | snp | C/T | | | | | GRCh38.p7 | 7:95459792 | GGGGCTATTTTCTGT[C/T]GGTGACTACTGGTGT | 51666 |
rs773689731 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95492094 | CTACCTACACACATT[C/T]CTATCTTAGGAGAGG | 51666 |
rs773697499 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95490885 | CTTCTCAAATTCCTT[C/T]AGAACTTTTAGCTAC | 51666 |
rs773741911 | snp | C/G/T | 5.22665e-05 | 0.00511185 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95537806 | TATTTAAGTGGACTT[C/G/T]CTGGGTAGACACAGT | 51666 |
rs773757488 | snp | A/G | 6.59467e-05 | 0.00574187 | synonymous-codon, intron-variant | ASB4 | GRCh38.p7 | 7:95537687 | CAGATGCCATAGAGC[A/G]ATTCCTTTGCTTTCC | 51666 |
rs773774931 | in-del | -/CC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95533241 | AGAAGCTGTGTATGG[-/CC]CCCCCTAACTAAACA | 51666 |
rs773859569 | snp | C/T | 1.67736e-05 | 0.00289595 | missense | ASB4 | GRCh38.p7 | 7:95527822 | TTATAGGGGCGAATG[C/T]GAACATGAAGACCAA | 51666 |
rs773865308 | snp | G/T | 4.94858e-05 | 0.00497398 | missense, intron-variant | ASB4 | GRCh38.p7 | 7:95537704 | TTCCTTTGCTTTCCC[G/T]CCCATTGTCATTGAA | 51666 |
rs773874262 | snp | C/T | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538167 | TAGCAGGCTTTGCAA[C/T]TGGCCTCTTAAACTT | 51666 |
rs773947850 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95502561 | TATCTCTGAACTAGG[C/T]TATACCTAAAGTCAA | 51666 |
rs774036632 | snp | A/C | | | | | GRCh38.p7 | 7:95477664 | TTATGCAATTTTGTG[A/C]AAACATGTAAGTGAG | 51666 |
rs774062645 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95535626 | GTAGTTTAATCTAAA[C/T]GTTAAAGCTAAATCT | 51666 |
rs774071511 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95509735 | AAAGGAAAATAATAT[A/G]TATTAAGCATCTATG | 51666 |
rs774084444 | in-del | -/TGTGTGTGTGTA | | | intron-variant | ASB4 | GRCh38.p7 | 7:95493380 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGTA]TGTGTGTGTGTATGT | 51666 |
rs774090714 | snp | C/T | | | | | GRCh38.p7 | 7:95464937 | ACAATAAGTTATTTT[C/T]CTCAATATTAAATTC | 51666 |
rs774184578 | snp | A/G | | | | | GRCh38.p7 | 7:95478890 | AGAATGAATACGCCG[A/G]ACTTTAGCGCTGAAG | 51666 |
rs774196248 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95511379 | TGGCAGCCCTCAGCA[A/G]CACTCTTGAATTAAG | 51666 |
rs774357093 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95518392 | AGAGATGGCGAAGCC[A/G]TAAGACCAAGGCAGC | 51666 |
rs774364360 | snp | C/G | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469318 | ATGAGGAAACTGAAG[C/G]CCTGAGGAGGCAAAA | 51666 |
rs774398851 | snp | A/C | 4.94645e-05 | 0.00497291 | missense | ASB4 | GRCh38.p7 | 7:95528131 | ACCACGTGCTCATGC[A/C]CATGATGCTGGAAGC | 51666 |
rs774402276 | in-del | GAGACGGAGTCTCGCTTTG/TTGGGGGGGTTCC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95499892 | TTTTTTTTTTTTTTT[lengthTooLong]TCGCCTGGGCTGGAG | 51666 |
rs774445879 | snp | C/T | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95485365 | CTAAAAGAGTCCCTG[C/T]CCCGGACCGTCTCCC | 51666 |
rs774446517 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95499754 | AAAAGCTTGTGTGCT[A/C]AAGGAAATGATTCAT | 51666 |
rs774448844 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95530362 | CCCAGCTACTTGGGA[A/G]GCTGAGGCAGGAGAA | 51666 |
rs774481152 | in-del | -/A | | | intron-variant | ASB4 | GRCh38.p7 | 7:95517602 | CACCCAAGGAAACTG[-/A]AAAAAAAAAAGAATT | 51666 |
rs774506865 | snp | A/G | 1.64906e-05 | 0.00287142 | missense | ASB4 | GRCh38.p7 | 7:95495868 | CTGGACCACAATGCT[A/G]CAATCAACTGTAGAC | 51666 |
rs774509798 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95531587 | ATGATGGCTATGACT[A/G]TTACTATTCTTAAAC | 51666 |
rs774534740 | snp | A/G | 1.6611e-05 | 0.00288188 | missense | ASB4 | GRCh38.p7 | 7:95536527 | ACAAAGTGGAGAAGA[A/G]CTATCCCCGATGATG | 51666 |
rs774537412 | in-del | -/A | 6.86772e-05 | 0.00585951 | intron-variant | ASB4 | GRCh38.p7 | 7:95486204 | GTTAGAAAATGATTT[-/A]AAAAAATGCACAGTG | 51666 |
rs774583484 | snp | A/G | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473016 | AATGATTGCTCACCA[A/G]TGGCAAGTTTCCATG | 51666 |
rs774647374 | in-del | -/TG | | | intron-variant | ASB4 | GRCh38.p7 | 7:95503345 | TGGAAACTAAAAGAC[-/TG]TGAGCATCTTGTTTT | 51666 |
rs774700744 | snp | G/T | | | | | GRCh38.p7 | 7:95480497 | ATATGACTTCCTAGG[G/T]TAGGTCACAAAAGAT | 51666 |
rs774708257 | snp | A/C | | | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95474263 | TACACATTTATTTTT[A/C]TTGGCTATTTATATT | 51666 |
rs774715779 | in-del | -/T | 1.65111e-05 | 0.0028732 | frameshift-variant | ASB4 | GRCh38.p7 | 7:95528273 | GTTGAACCATGGGGC[-/T]GCCCGAATATACCCT | 51666 |
rs774742825 | snp | C/T | | | | | GRCh38.p7 | 7:95476283 | AGGCTTCCAGCCCAG[C/T]CCAGAGTCATCGGAT | 51666 |
rs774754745 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95526844 | AGAGTTGGCCCCCTA[A/C]GGGTCATTTGGTTCA | 51666 |
rs774758903 | snp | A/T | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469635 | TCAATTGCCTACTTA[A/T]ACTTTTATAATTATT | 51666 |
rs774765680 | snp | A/C/G | 3.36798e-05 | 0.00410353 | missense | ASB4 | GRCh38.p7 | 7:95536446 | CTGCAGGTGATACAG[A/C/G]CCTGCCATTCTTGTC | 51666 |
rs774797790 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95523648 | AACATAGTTCAAATG[C/T]TTCAGCTTAATAATT | 51666 |
rs774825487 | snp | A/G | | | | | GRCh38.p7 | 7:95481647 | GCCATGATAAACCAA[A/G]GAGCCATTTGTGTTC | 51666 |
rs774863107 | snp | C/G | 1.64944e-05 | 0.00287175 | stop-gained | ASB4 | GRCh38.p7 | 7:95528006 | TAAGGAGCAGGAGTA[C/G]AGCACGGAGCACCAC | 51666 |
rs774875478 | in-del | -/C | | | nc-transcript-variant, intron-variant | LOC107986823 | GRCh38.p7 | 7:95471098 | TTCTCATTTTTCTGT[-/C]CCCTTGGCTCATTTC | 51666 |
rs774898925 | snp | A/G | 1.64988e-05 | 0.00287213 | missense | ASB4 | GRCh38.p7 | 7:95527918 | TCTACGTGGAACACG[A/G]GGCCATAGTGGACAG | 51666 |
rs774920119 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95510179 | TGTGTTTAATGAAAA[G/T]ATATGAAAAACTGTC | 51666 |
rs774971843 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95490015 | ACTTATCTCTTTGGT[A/T]TGAAATTCCCTAGTC | 51666 |
rs774995198 | snp | G/T | | | | | GRCh38.p7 | 7:95482417 | ATGTTCCCTGTGGCC[G/T]TTGACCTTGAGGGCC | 51666 |
rs775025264 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513089 | ATAGGATGTATAAGA[A/G]ATTCTACCCACCATT | 51666 |
rs775088922 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95506176 | GTGCTGGAATTATAG[A/G]TGTGAGGCATTGTAC | 51666 |
rs775089807 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95512859 | GTTAGGAAGAAAAAC[C/G]ACCCTCCAAAGATGT | 51666 |
rs775104111 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95496316 | TAGCTCCTATTATGC[A/C]TCAGGTAATGCACTA | 51666 |
rs775198339 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95531715 | ACTAAATGTTGACTT[G/T]TATTCTGAAACTTGC | 51666 |
rs775225728 | snp | A/G | 4.96249e-05 | 0.00498096 | missense | ASB4 | GRCh38.p7 | 7:95486143 | GAGAATATGGTTTTG[A/G]CATCTTATAAACAAG | 51666 |
rs775311890 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95501633 | TGTAACTGAAACTTT[C/G]TTAACTTTTTACATT | 51666 |
rs775399940 | snp | A/G | 1.64982e-05 | 0.00287208 | missense | ASB4 | GRCh38.p7 | 7:95528238 | CCTGCTGCCCAGCCT[A/G]AGATCTGCTACCAGC | 51666 |
rs775416925 | in-del | -/TGGAGGTAA | 1.66305e-05 | 0.00288357 | cds-indel | ASB4 | GRCh38.p7 | 7:95536529 | AAGTGGAGAAGAGCT[-/TGGAGGTAA]ATCCCCGATGATGAC | 51666 |
rs775450097 | snp | C/T | | | | | GRCh38.p7 | 7:95475542 | GTGCGTGCCACCACA[C/T]CTGGCTAAGTTTTGT | 51666 |
rs775529507 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95532952 | CCCTTTGGGGTCCAC[A/G]TCAGTCTGCTGTCTC | 51666 |
rs775580416 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95505928 | AGACAGGGTTTCACT[C/G]TGTCACCCAGGCTAG | 51666 |
rs775601815 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95518711 | GATGATGTACAAATC[C/T]TTAACAGGGATTCCA | 51666 |
rs775602815 | snp | G/T | | | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95474511 | AGTTTAAAATCCTAT[G/T]TTAAAACTTAGTTTT | 51666 |
rs775608741 | in-del | -/T | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538260 | CCCAAACCAAGCTAC[-/T]CAAGTTTATTTCAGT | 51666 |
rs775656209 | snp | C/T | | | | | GRCh38.p7 | 7:95461123 | CCCCTCACAGAGTCC[C/T]CACTGGGGCACTGCC | 51666 |
rs775661385 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513194 | GAAATGGACTCTTCT[A/G]TACATTCTGGTTGAC | 51666 |
rs775666631 | in-del | -/T | 1.64789e-05 | 0.0028704 | frameshift-variant | ASB4 | GRCh38.p7 | 7:95486100 | CCAAAGGCAAATAGA[-/T]GTGGACACTGTTTTT | 51666 |
rs775674912 | snp | C/T | | | | | GRCh38.p7 | 7:95481839 | GAGCAAAGGACACTG[C/T]TCTGGACATGTAATG | 51666 |
rs775680130 | snp | C/T | | | | | GRCh38.p7 | 7:95468728 | TTGTGTATGACTAGA[C/T]GTAAGTGGGTACTAA | 51666 |
rs775712844 | snp | C/T | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539062 | ATGAGGTCAATTTTG[C/T]TTCACTTTTTTTTTT | 51666 |
rs775777988 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95506939 | ATCTTGTATTGTCTC[A/G]TCTCTCCTATTTTAT | 51666 |
rs775827567 | in-del | -/AAAC | | | | | GRCh38.p7 | 7:95465942 | CCCTGTTTCTGAAAC[-/AAAC]AAACAAACAAACAAA | 51666 |
rs775832267 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515455 | AGAGTCTCATTCTGT[C/T]GCTAGGTTGGAGTGC | 51666 |
rs775847326 | snp | C/T | 1.67091e-05 | 0.00289038 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95536535 | GAGAAGAGCTATCCC[C/T]GATGATGACTTGGAG | 51666 |
rs775860674 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95526916 | AGTTGACCACTCTCA[C/T]ATTTAACATTTCTAA | 51666 |
rs775887041 | snp | A/G | | | | | GRCh38.p7 | 7:95460981 | GCCATTGCTTCAGAG[A/G]GTGCAAGCCCCAAGC | 51666 |
rs775892510 | snp | A/G | 4.94711e-05 | 0.00497324 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95528141 | CATGCACATGATGCT[A/G]GAAGCTGGCGCCGAA | 51666 |
rs775919430 | in-del | -/AA | | | intron-variant | ASB4 | GRCh38.p7 | 7:95500573 | GATCTGTCTCAAAAA[-/AA]AAAAAAAAAAAAAAA | 51666 |
rs775934162 | snp | A/C | | | | | GRCh38.p7 | 7:95482906 | AGATATGCCTGAGGA[A/C]GTTCGAGGACACTGA | 51666 |
rs775936504 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95512191 | ACATGGCTTGATATG[A/C]AAAGAGGAACTCAAG | 51666 |
rs775951581 | snp | C/T | 1.67447e-05 | 0.00289345 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95536451 | GGTGATACAGGCCTG[C/T]CATTCTTGTCCTAAA | 51666 |
rs775983366 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95514081 | CTCTCCAGTATTTTC[A/G]CTTCTTATCTTTCCA | 51666 |
rs776104910 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95514566 | CTGGCTTCAGGGTAC[A/C]CAAATTCTCCCTCCC | 51666 |
rs776195005 | in-del | -/A | | | intron-variant | ASB4 | GRCh38.p7 | 7:95488018 | TGTCTCTTTAGTCTT[-/A]AAACCCAGGTTAAAA | 51666 |
rs776259872 | in-del | -/CTC | | | intron-variant, cds-indel | ASB4 | GRCh38.p7 | 7:95528459 | CCTAATCCTAGCTGT[-/CTC]CTCATCTCATCCTAG | 51666 |
rs776295453 | snp | A/T | | | | | GRCh38.p7 | 7:95468445 | ACAGAAGACCATGCA[A/T]GTAATGGAGGGAGCT | 51666 |
rs776303190 | in-del | -/AGAGCTGA | | | intron-variant | ASB4 | GRCh38.p7 | 7:95532257 | ACAAGGAACAAGGTC[-/AGAGCTGA]AGATGTTTTCTTCCA | 51666 |
rs776338052 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95520618 | TTTAATTTATCTGAA[A/G]TTAAACACACACTCC | 51666 |
rs776341105 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95500190 | ATTTTCATAAGAATG[A/G]AGAAGGAATGGGAGG | 51666 |
rs776342693 | snp | A/C | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469427 | CCAGAAACCAATTTC[A/C]TATGTGTCAGGTAAT | 51666 |
rs776370962 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95532095 | CAATTTACTATGCAG[A/C]TGCTTCAAAGTGATT | 51666 |
rs776418260 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95487986 | ACTCTGTTTAATACG[C/T]ACATGGGCACAAGGA | 51666 |
rs776470206 | snp | G/T | 1.64953e-05 | 0.00287182 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95528012 | GCAGGAGTACAGCAC[G/T]GAGCACCACCTGGTC | 51666 |
rs776536235 | snp | A/C | | | | | GRCh38.p7 | 7:95475682 | AGCCACCGTGCCCGG[A/C]CTTGAATTTATTTAA | 51666 |
rs776609639 | snp | C/T | 0.000685212 | 0.0184969 | intron-variant | ASB4 | GRCh38.p7 | 7:95495748 | TTTTCCTTTTTTTTT[C/T]TTTTTTCAGGTTACT | 51666 |
rs776770733 | snp | A/G | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539297 | AACTGGCAATCACCT[A/G]ACTGGTTAATCTCAG | 51666 |
rs776775569 | snp | C/T | 4.00424e-05 | 0.00447433 | intron-variant | ASB4 | GRCh38.p7 | 7:95527788 | ACATGTTTAAATAAT[C/T]GTCTTCCTCAATTTC | 51666 |
rs776796533 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95508389 | GTGAAAAGAGAAGAA[A/G]TATAAAAGATCTGAG | 51666 |
rs776824697 | snp | A/G | | | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95471230 | ACGTCCCCTTCAAAT[A/G]ATGTGGCTTGCCCCA | 51666 |
rs776903358 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95533305 | ATTCTGATCTCTGAT[G/T]GTCATCTTCATTTCA | 51666 |
rs776917876 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95495150 | AATCTTTAAGTGTGT[C/G]AAAGTTGAGAGTTGC | 51666 |
rs776923045 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515661 | CCTTGTGATCCCCCC[A/G]ACCTTGGCCTCCCAA | 51666 |
rs776972630 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95504057 | ACCCTGCTGAAAAAC[C/T]TCCTCTCCTTGAATC | 51666 |
rs776974896 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95496444 | TAAATTGGGACAGTG[C/T]TTTGAAGGAGAAAAC | 51666 |
rs777014503 | snp | C/T | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95483737 | AGGGATTTCTGTGTT[C/T]GTTCACTGCTGTATC | 51666 |
rs777025950 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95531474 | CACTTTATCCATGAA[C/T]AGTAATAGCCTTCTT | 51666 |
rs777037413 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95516803 | CTCTTTTCTGTGTTT[A/C]AATATTTGCATGTCC | 51666 |
rs777041944 | snp | A/G | 1.72644e-05 | 0.00293801 | intron-variant | ASB4 | GRCh38.p7 | 7:95536553 | TGATGACTTGGAGGT[A/G]AATAATCGATTCCCT | 51666 |
rs777057452 | snp | A/T | 1.64857e-05 | 0.00287099 | missense | ASB4 | GRCh38.p7 | 7:95495987 | TTGCTACTCCTTAAG[A/T]GGACACACAGCTTTG | 51666 |
rs777112510 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95502887 | CCTCAGAGAGTCATT[C/T]ATATTACTGAAAAAC | 51666 |
rs777143794 | snp | C/T | | | | | GRCh38.p7 | 7:95459688 | TTGCTTGGTATTCAA[C/T]CAAAGAACAGGCAGA | 51666 |
rs777219552 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95529588 | CTGTGATCTCAATAG[A/G]AATTTTCTCTTGGTT | 51666 |
rs777282234 | snp | C/T | 5.88137e-05 | 0.00542249 | intron-variant | ASB4 | GRCh38.p7 | 7:95527791 | TGTTTAAATAATTGT[C/T]TTCCTCAATTTCCCT | 51666 |
rs777284535 | snp | A/C | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95483505 | CACATCAGGTTGGAC[A/C]AAATTAAATTGTCCT | 51666 |
rs777290346 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95527506 | TGTAGAAATCTCTTG[C/G]TATTTCCAAATCCAC | 51666 |
rs777300165 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95535708 | TTTGGTTGGTTAATA[A/T]ACTATTAAACAGAGT | 51666 |
rs777369309 | snp | C/T | 2.47307e-05 | 0.00351636 | intron-variant, utr-variant-3-prime | ASB4 | GRCh38.p7 | 7:95528420 | GCTAACTACCTCTGA[C/T]CCTCTTTGACCTTCC | 51666 |
rs777443878 | snp | C/T | | | | | GRCh38.p7 | 7:95460752 | TGAGGAGCCAAATGT[C/T]AATCACCAAGACAAT | 51666 |
rs777447764 | in-del | -/A | | | intron-variant | ASB4 | GRCh38.p7 | 7:95502131 | GAGAGAGAAAGAGGT[-/A]AAAAAAAGAAAAAGA | 51666 |
rs777451184 | snp | C/G | 3.29652e-05 | 0.00405974 | missense | ASB4 | GRCh38.p7 | 7:95486110 | ATAGATGTGGACACT[C/G]TTTTTGAAGTCGAAG | 51666 |
rs777500646 | in-del | -/T | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473640 | TAATTTGGAGATTCC[-/T]TTTTTTTTTTTTTTT | 51666 |
rs777538321 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95529811 | TTTTTATAATGGACT[C/T]TGAGGTGGGCACTGG | 51666 |
rs777545123 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95516778 | TCAGTCTTATTTGCT[G/T]GATCTGCTACTCTTT | 51666 |
rs777547543 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95516473 | GTAAGTTAAAAATAA[A/G]CAAAATGATAAATAA | 51666 |
rs777566703 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95491514 | GGCTTTTGAAAGACA[A/C]ATACTAGGAATAAAT | 51666 |
rs777589865 | snp | C/T | 1.7081e-05 | 0.00292237 | intron-variant | ASB4 | GRCh38.p7 | 7:95496080 | TTTCTGGGTGGCCAA[C/T]ATTGTTGTCTGCTTG | 51666 |
rs777605026 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95536295 | GCTCAAGCAATCCTC[C/T]TGCCTCAGTCTCCCA | 51666 |
rs777616006 | snp | G/T | | | | | GRCh38.p7 | 7:95480119 | TTTTCTTACTTGTTG[G/T]TCCACAGGAGCACAC | 51666 |
rs777640563 | snp | A/G | 1.64895e-05 | 0.00287132 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95495960 | CCTCTGTGATCGTGG[A/G]GCAAAGCTCAATTGC | 51666 |
rs777660247 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95524034 | AGAAACCCTCACCCA[C/T]GGCTTATCGGAGTGT | 51666 |
rs777662599 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95511295 | TGCAGGGAAGGCCCA[A/G]TTAGGGAGTCCCCTG | 51666 |
rs777668038 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95503755 | CCGTTAGAGGAAGAA[C/T]CAATGCCATGGCAAC | 51666 |
rs777672033 | snp | A/C | | | | | GRCh38.p7 | 7:95478808 | AGCAATCATTTCTGC[A/C]ATTTGTGAGGATTGT | 51666 |
rs777675244 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95492881 | AGTTAATGTGATTCG[A/T]TCATCATCAAAAGCA | 51666 |
rs777786777 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95524928 | GTAAGATGGGGGCCT[A/G]TTAACAGGAACCCCT | 51666 |
rs777858607 | snp | A/G | | | | | GRCh38.p7 | 7:95467744 | CCACCTGTGGGCAGT[A/G]CAAAGGTTCCTGAAC | 51666 |
rs777915990 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95512619 | AAAGATACAAAGGTA[C/T]ATAAAATCTACACAT | 51666 |
rs777955438 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95534641 | TCTTCTCCTCTGTGG[A/G]TTGCTGATGGTGCTC | 51666 |
rs777985952 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95520257 | GAAGTTACGGACAAA[A/G]GGAGCAGAAACAAAA | 51666 |
rs778008852 | in-del | -/G | | | frameshift-variant | ASB4 | GRCh38.p7 | 7:95528063 | AAAGCCGAAGTCAAT[-/G]GCCCGAGATGACGAC | 51666 |
rs778039684 | snp | C/G/T | 3.30002e-05 | 0.00406192 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95527970 | CCCCCTGGCCATCGC[C/G/T]GCCTACTGGGCCCTC | 51666 |
rs778062407 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95519607 | AGATAAAATAAACAA[C/T]TAATGAGGATTCTGG | 51666 |
rs778074001 | snp | C/T | 6.91695e-05 | 0.00588047 | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95537799 | TCCTAGGTATTTAAG[C/T]GGACTTGCTGGGTAG | 51666 |
rs778083506 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95531441 | AGGGCATGAAGGTGC[C/T]AGAGAAACATACTCT | 51666 |
rs778089776 | in-del | -/TGTGTGT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95493385 | GTGTGTGTGTGTGTG[-/TGTGTGT]ATGTGTGTGTGTGTG | 51666 |
rs778209748 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95498620 | GATACATAGTTTGCA[C/T]GTATTTCTCTTCATT | 51666 |
rs778250717 | snp | C/G | 7.47189e-05 | 0.00611178 | intron-variant | ASB4 | GRCh38.p7 | 7:95495712 | CAGGGAGAAAGCCTA[C/G]GTCAAGAAGTTAAAC | 51666 |
rs778304526 | snp | G/T | | | nc-transcript-variant | LOC107986823 | GRCh38.p7 | 7:95474074 | ATGTGTGGTATTTGC[G/T]AAAAGTTGGGGCGCA | 51666 |
rs778304656 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95487200 | GGGACATATAGAAGA[A/G]CTCAGGCTAGTTACT | 51666 |
rs778347940 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95531071 | GCAGACTCAGTCCTT[C/T]CCCAGAAGGAAGTTA | 51666 |
rs778353948 | snp | C/G | | | | | GRCh38.p7 | 7:95475339 | TAAAATCACAACCTA[C/G]AATATTGGCAGTGGT | 51666 |
rs778359982 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95486203 | TGTTAGAAAATGATT[A/T]AAAAAAATGCACAGT | 51666 |
rs778400071 | snp | A/C | | | | | GRCh38.p7 | 7:95461892 | GGGGCTTAAAAGGGG[A/C]TTTTCCCCTTTTTGC | 51666 |
rs778407342 | snp | A/C | | | | | GRCh38.p7 | 7:95460267 | AACTGGGTAACAGGA[A/C]GAGGTTGGAACAGTT | 51666 |
rs778419668 | snp | C/T | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472680 | CAAAAAGGCTCAGGA[C/T]AGGCTCTGAATTCCA | 51666 |
rs778490115 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95503966 | TGTTTGCCTTTCTAC[G/T]TAATGCCCCCATCTC | 51666 |
rs778508330 | snp | C/T | 1.64931e-05 | 0.00287163 | missense | ASB4 | GRCh38.p7 | 7:95495808 | TGGGCCACAGGCCTC[C/T]ATCTCTCTGTCTTGT | 51666 |
rs778595628 | snp | A/G | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484326 | ACAGAGTGAGATCCT[A/G]TCTCAAAAAAAAATA | 51666 |
rs778625239 | in-del | -/TTAA | | | intron-variant | ASB4 | GRCh38.p7 | 7:95529302 | CCTTGCTCTAAAAAT[-/TTAA]TTAACAACAAGAAGA | 51666 |
rs778664066 | in-del | -/A | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469290 | AGAATTTTTGAGGTC[-/A]AAAGGCCCTCAGATG | 51666 |
rs778686566 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95514091 | TTTTCGCTTCTTATC[C/T]TTCCATCATTCTCTC | 51666 |
rs778767666 | snp | C/T | | | upstream-variant-2KB | LOC107986823 | GRCh38.p7 | 7:95469057 | ACAAAGTTCATTCCA[C/T]TTGTTTGGAGCTGGG | 51666 |
rs778770020 | snp | C/G | 1.67897e-05 | 0.00289733 | intron-variant, missense | ASB4 | GRCh38.p7 | 7:95528336 | GGTCAGCAGGTTGAG[C/G]AAGATTCAAATGGCA | 51666 |
rs778816677 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95499574 | TTAAAAGCCAGATTT[C/G]AATGGTATAAAGTGC | 51666 |
rs778868555 | snp | A/G | | | | | GRCh38.p7 | 7:95480148 | ACCTTGTTCTGATCT[A/G]TACAAGGGTGGCTTA | 51666 |
rs778871789 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95486167 | AAACAAGGTAAAAAC[A/G]TATAGGTGTTATTGT | 51666 |
rs778909324 | snp | A/T | | | | | GRCh38.p7 | 7:95467966 | AGCCCATACCTTTCA[A/T]TAGATTCTCAAAGCA | 51666 |
rs778924598 | snp | A/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513608 | TAGAAAAACAACATC[A/T]CAGAAACATCCAGAA | 51666 |
rs778941042 | snp | G/T | 1.75801e-05 | 0.00296475 | utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485960 | AACAAAGCTTCCAGA[G/T]GGAGAGGAAGGATGG | 51666 |
rs778977490 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95500373 | GGAGTTTGAGATCAG[A/G]CTGGGCAACATAGTG | 51666 |
rs779007755 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95527190 | GTGTGTGTGTGCATG[C/T]GTATGTGTGTGTGTG | 51666 |
rs779150910 | snp | G/T | 1.75857e-05 | 0.00296522 | intron-variant | ASB4 | GRCh38.p7 | 7:95537552 | TGCTAACTTTAATTT[G/T]TCTTGCCTTCCTTTT | 51666 |
rs779167677 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95519787 | CAGCCATTAGTGATT[C/T]ACTATGTTTTAAGTC | 51666 |
rs779170682 | snp | C/G | | | | | GRCh38.p7 | 7:95476644 | CTCCATCTGTGGCTT[C/G]ACGCCTTTTTAGAAA | 51666 |
rs779190085 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95487474 | CTCAGGTTCAAGTCA[C/G]TGGGTAAGTTATTTG | 51666 |
rs779193171 | snp | C/G/T | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538926 | AAAAGTAAATAGAGA[C/G/T]ACTTTTTGAAAATGG | 51666 |
rs779205172 | snp | A/C | 1.64955e-05 | 0.00287184 | missense | ASB4 | GRCh38.p7 | 7:95527998 | CTCCGCTTTAAGGAG[A/C]AGGAGTACAGCACGG | 51666 |
rs779260293 | snp | A/C | | | missense | ASB4 | GRCh38.p7 | 7:95528053 | TGCTTGACTACAAAG[A/C]CGAAGTCAATGCCCG | 51666 |
rs779267305 | in-del | -/TT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515218 | TTCTTTCTTTCTTTC[-/TT]TCTTTCTTTCTTTTT | 51666 |
rs779324407 | snp | C/T | | | | | GRCh38.p7 | 7:95475530 | CTGGGACTACAGGTG[C/T]GTGCCACCACACCTG | 51666 |
rs779435277 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95495660 | CCACTTTTATAAATG[C/T]GGCCAAAATAAAATA | 51666 |
rs779437038 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95506409 | TTTTCTGGACCACAA[G/T]TCTTCCTAAATCTTG | 51666 |
rs779461066 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95509185 | AAGATAATTATATTC[A/G]GGAAGGAGATTAGGT | 51666 |
rs779506274 | snp | A/G | | | downstream-variant-500B, intron-variant | ASB4 | GRCh38.p7 | 7:95540258 | TTACTTACCAATAAG[A/G]CTCTTTTTCCTAACC | 51666 |
rs779514547 | snp | A/G | | | | | GRCh38.p7 | 7:95461636 | ACTTTGGGGACTGTT[A/G]GAAGGGCATGATTGT | 51666 |
rs779517506 | snp | C/T | 3.2981e-05 | 0.00406071 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95495927 | TTGTGAAATGGCCAA[C/T]GTGGATTGTGTTAAG | 51666 |
rs779569501 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95505199 | ACAGGATGTTTGTCT[A/G]CATGGAAAATCCAAG | 51666 |
rs779578823 | snp | A/T | | | | | GRCh38.p7 | 7:95460703 | CATTTTCTGGGGAGA[A/T]ATTCAAGCCAGCTGC | 51666 |
rs779622287 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95491926 | CAGGGCTGAATTATT[C/T]AAAAATCCCTAGCCC | 51666 |
rs779697877 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95509877 | GATAAGTTGAATCAG[A/G]CCTCAGTACAAAGCT | 51666 |
rs779783287 | snp | A/G | 1.87704e-05 | 0.00306347 | intron-variant | ASB4 | GRCh38.p7 | 7:95536414 | GTGCATCAAACAGAT[A/G]AAACTCTGTGCTTCC | 51666 |
rs779836279 | snp | A/C | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484131 | TTAGGAGTCGGAGAT[A/C]AGCCGGGGGAACATG | 51666 |
rs779836593 | snp | C/T | 3.72273e-05 | 0.00431419 | intron-variant | ASB4 | GRCh38.p7 | 7:95495731 | AAGAAGTTAAACTTT[C/T]CTTTTCCTTTTTTTT | 51666 |
rs779836680 | snp | A/G | 1.65548e-05 | 0.002877 | missense | ASB4 | GRCh38.p7 | 7:95536512 | CACATCAGATGGAAC[A/G]CAAAGTGGAGAAGAG | 51666 |
rs779880243 | snp | A/G | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538767 | GGCTCCAGTGCATGT[A/G]ACAAGGAAGCATAGG | 51666 |
rs779894283 | snp | A/G | | | | | GRCh38.p7 | 7:95481238 | AACACTACAACTGGA[A/G]TTTTCCATTATAGGA | 51666 |
rs779948546 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95537516 | CATTGCTGATTTTTA[C/T]TGATGTAAACTGTGG | 51666 |
rs779964497 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513814 | TAGGACTCTCACCTA[C/T]CCACCCTAGGCATCC | 51666 |
rs780009942 | snp | C/T | 1.67511e-05 | 0.00289401 | missense, intron-variant | ASB4 | GRCh38.p7 | 7:95537754 | CCAGAGGGAATTATT[C/T]ATTAAGCCTTATGAG | 51666 |
rs780065450 | snp | C/T | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95473365 | TATCTCCATTTTAGA[C/T]GTGAAGGACCCAAGG | 51666 |
rs780069607 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95487806 | AGGGAGATAGCAAAT[G/T]ACACCCTCTGGAAAA | 51666 |
rs780122082 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95488914 | AACCTATAACGAATC[C/T]CATGCTACTCTTAAA | 51666 |
rs780188899 | snp | C/T | | | | | GRCh38.p7 | 7:95478384 | ACAGAGCTAATGCCC[C/T]CTCTGTGGGGCAGGG | 51666 |
rs780238414 | snp | A/G | 1.64871e-05 | 0.00287111 | missense, intron-variant | ASB4 | GRCh38.p7 | 7:95537647 | TGCACTTATCGAGAT[A/G]TGCCATTAGAAGAAC | 51666 |
rs780248904 | snp | C/G | 0.00032987 | 0.0128385 | missense | ASB4 | GRCh38.p7 | 7:95528185 | ATATCAACGGCTGTG[C/G]TGCCATCCAGTACGT | 51666 |
rs780274828 | snp | A/G | | | | | GRCh38.p7 | 7:95460733 | CAGAAAGTTGCACAA[A/G]TAATGAGGAGCCAAA | 51666 |
rs780291223 | snp | G/T | 3.48396e-05 | 0.00417356 | intron-variant | ASB4 | GRCh38.p7 | 7:95496101 | TGTCTGCTTGTACAC[G/T]CATGGTTTCAAGACT | 51666 |
rs780314649 | snp | C/T | | | | | GRCh38.p7 | 7:95466244 | ATAGCCAGTCAAAGC[C/T]ACACAGTTCTAAGAG | 51666 |
rs780319223 | snp | A/G | | | | | GRCh38.p7 | 7:95476920 | CAATGTTTAATTTAT[A/G]TATTTGTTAGATACA | 51666 |
rs780333964 | snp | C/T | | | downstream-variant-500B, intron-variant | ASB4 | GRCh38.p7 | 7:95540513 | CTCTGCCTCTCACCA[C/T]CTCTGTCCTCCTGGG | 51666 |
rs780348714 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95521657 | TAAACTGTGGTTTAT[A/G]CAAGGTAATTCTGTT | 51666 |
rs780498293 | in-del | -/AAG | | | intron-variant | ASB4 | GRCh38.p7 | 7:95494709 | TGGCATTGACATAGA[-/AAG]AAGGTTTATAAAGTC | 51666 |
rs780505034 | in-del | -/T | 3.29938e-05 | 0.0040615 | frameshift-variant | ASB4 | GRCh38.p7 | 7:95527960 | ACATGGAGACCCCCC[-/T]GGCCATCGCCGCCTA | 51666 |
rs780578403 | snp | A/G | | | downstream-variant-500B, intron-variant | ASB4 | GRCh38.p7 | 7:95540447 | GCAGCCTCTTGCTGT[A/G]AGAACAAGTGTGTTT | 51666 |
rs780598821 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95497133 | AGGGTCAAAGTGTAG[C/G]GCTCTGAAATGGAGC | 51666 |
rs780619895 | in-del | -/A | 1.72809e-05 | 0.00293941 | splice-acceptor-variant | ASB4 | GRCh38.p7 | 7:95527811 | TCAATTTCCCTTTAT[-/A]GGGGCGAATGTGAAC | 51666 |
rs780623147 | snp | C/T | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539971 | CCCTGCATCTTAAGG[C/T]GTATTCTAGCAGCAA | 51666 |
rs780638220 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95507491 | TCCCAATGCTATGTT[A/C]TGTATTCTCATAGCA | 51666 |
rs780654414 | snp | A/G | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484679 | ATTATTCTGCAGAAA[A/G]TTTGCACCAGTTTTG | 51666 |
rs780660450 | in-del | -/TC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515237 | TTCTTTCTTTTTCTT[-/TC]TCTTTCTTTCTTTCC | 51666 |
rs780674281 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95513940 | TCCACGAAGGATTTC[A/G]ATGCTGGCATAAATT | 51666 |
rs780686793 | snp | A/G | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95538820 | TGAGGGGACCTAGTT[A/G]ATTACTTCGGTCTTT | 51666 |
rs780709575 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95505786 | TTCTTTTTTTGTGCA[A/C]TGTTTGTTATCTCTG | 51666 |
rs780764847 | snp | A/G | | | | | GRCh38.p7 | 7:95481493 | ACATCTAATTCAGCT[A/G]CTGAGAAAGTCAGGA | 51666 |
rs780865545 | snp | A/C/G | 3.29909e-05 | 0.00406135 | missense | ASB4 | GRCh38.p7 | 7:95528208 | CAGTACGTGCTGAAG[A/C/G]TCACCTCCGTGCGCC | 51666 |
rs780934268 | snp | A/T | | | | | GRCh38.p7 | 7:95464488 | AGTGCTTGAAAATAA[A/T]GCTTAAACATCGCCC | 51666 |
rs780946554 | snp | A/G | | | | | GRCh38.p7 | 7:95483286 | GATACACGTGGTCTG[A/G]CCATACTGGTAATTT | 51666 |
rs780974649 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95503559 | CTGCTCTTCATCAGT[C/T]TTACCCTCTCAGTCT | 51666 |
rs780991883 | snp | A/C/T | 4.94697e-05 | 0.00497321 | missense | ASB4 | GRCh38.p7 | 7:95495955 | AAGATCCTCTGTGAT[A/C/T]GTGGGGCAAAGCTCA | 51666 |
rs781012077 | snp | A/G | 1.87412e-05 | 0.00306108 | intron-variant | ASB4 | GRCh38.p7 | 7:95536589 | TAGTTTTCACTATCA[A/G]GTACTTCCAGACTGC | 51666 |
rs781023458 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95535316 | GGAAATTAGGAAGAA[A/G]TGTCTTTGGAGAAAG | 51666 |
rs781029727 | snp | A/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95490072 | TAATCAGGGTAATGC[A/C]CTTTAAGTACTTCGT | 51666 |
rs781050548 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95502046 | AAAATATTTGAGACT[A/G]TATGACAAAGGGCTT | 51666 |
rs781072582 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95522659 | GTTTAGTACCAGTCT[C/T]TTTCCACACAAAGGC | 51666 |
rs781082330 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95514712 | AGCGCAACCTGGAGT[C/T]CATGAAAATATTCTG | 51666 |
rs781089451 | snp | C/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95534147 | GTCATAAATTCAACA[C/G]CAGCCTTACCAACAT | 51666 |
rs781154467 | snp | A/G | 1.64982e-05 | 0.00287208 | synonymous-codon | ASB4 | GRCh38.p7 | 7:95527961 | CATGGAGACCCCCCT[A/G]GCCATCGCCGCCTAC | 51666 |
rs781178157 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95489255 | AAATATGAAATGTGT[A/G]TTTTGTGAGGAAGAC | 51666 |
rs781178629 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95499184 | AGTATAGATTTCAGA[A/G]CAGAGCCCTGGACTA | 51666 |
rs781264594 | snp | A/C | | | nc-transcript-variant, intron-variant | LOC107986823 | GRCh38.p7 | 7:95471332 | TCCTGCACGCTTCCT[A/C]ATTTGCAAAACAATG | 51666 |
rs781270544 | snp | C/T | | | | | GRCh38.p7 | 7:95478663 | GTTTGTTCGCTGATA[C/T]GGGATCCAAGAAGTG | 51666 |
rs781301858 | snp | A/G | 1.65075e-05 | 0.00287289 | missense | ASB4 | GRCh38.p7 | 7:95527882 | CGGCTGCCCACTTCG[A/G]CCTTTCGGAGCTGGT | 51666 |
rs781324812 | in-del | -/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515375 | TTCTTTTCTTTCTTT[-/T]CTTTTCTTTTCTTTT | 51666 |
rs781388687 | snp | C/T | 1.64773e-05 | 0.00287026 | stop-gained | ASB4 | GRCh38.p7 | 7:95486092 | ATTTTGATCCAAAGG[C/T]AAATAGATGTGGACA | 51666 |
rs781449470 | snp | A/C | | | | | GRCh38.p7 | 7:95467501 | GGGTATGCTAGAGGA[A/C]AGAGATCACAAGTCC | 51666 |
rs781535222 | in-del | -/TC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515312 | TTTCTTTCTTTCTTT[-/TC]CTTTCTTCCTTCCTT | 51666 |
rs781539523 | in-del | -/TC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515304 | CTTTCTTTCTTTCTT[-/TC]TTTCTTTCTTTCTTC | 51666 |
rs781654155 | in-del | -/GGACT | | | intron-variant | ASB4 | GRCh38.p7 | 7:95519813 | AAGTCATGCATTTGA[-/GGACT]GGAGTTAAAAATTTT | 51666 |
rs781758005 | snp | C/T | 1.67489e-05 | 0.00289381 | missense | ASB4 | GRCh38.p7 | 7:95485988 | TGGACGGCACCACTG[C/T]CCCTGTCACTAAATC | 51666 |
rs781764039 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | ASB4 | GRCh38.p7 | 7:95485812 | GTGACAGCCAAGAAG[A/G]ATATTTTGAAGTTTG | 51666 |
rs781781794 | snp | A/C | 1.65225e-05 | 0.00287419 | missense | ASB4 | GRCh38.p7 | 7:95528286 | GCTGCCCGAATATAC[A/C]CTCCACAGTTCCATA | 51666 |
rs796163888 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95522531 | TACATGTTAGGCAGG[A/G]CATTGTATTTATTTT | 51666 |
rs796166269 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95529635 | AAGATTAACTAATTC[C/T]TTTTTAAAAAATTAT | 51666 |
rs796178083 | in-del | -/TA | | | | | GRCh38.p7 | 7:95467559 | GTGTGTGTGTGTGTG[-/TA]TGTATGTGTTTATAG | 51666 |
rs796240723 | in-del | -/A | | | | | GRCh38.p7 | 7:95479092 | TGTTCCATAAGGGAG[-/A]AAAAAAGCCCTAAAG | 51666 |
rs796336066 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95511677 | CAAAAAAAAAAAATA[A/G]ATAAATAAAAATAAC | 51666 |
rs796400190 | snp | A/G | | | intron-variant | ASB4 | GRCh38.p7 | 7:95521791 | AAAACACAAAATAAT[A/G]GTATATTTTTTAAAT | 51666 |
rs796436164 | in-del | CAGATC/G | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95484125 | AAACTTAGGAGTCGG[CAGATC/G]GATCAGCCGGGGGAA | 51666 |
rs796553853 | in-del | -/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95511961 | TGGGTGACTTTGCTG[-/T]TTTTGCCTTATTCTG | 51666 |
rs796575554 | snp | G/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95496579 | CGGCCAGGTGCTGTG[G/T]CTCATGCTTGTGGTA | 51666 |
rs796577959 | in-del | -/A | | | intron-variant | ASB4 | GRCh38.p7 | 7:95534353 | CATTAAAAAAAAAAA[-/A]GATGAACTATCCTCC | 51666 |
rs796651732 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95536885 | ACCAGAATATTAAAG[C/T]GTTTTGTGTAGATTA | 51666 |
rs796652845 | snp | G/T | | | | | GRCh38.p7 | 7:95461737 | CTCAAATTTCATCTT[G/T]AATTGTAGTTCTCAT | 51666 |
rs796702343 | snp | C/T | | | upstream-variant-2KB | ASB4 | GRCh38.p7 | 7:95483774 | GCCCAGAATAAGTGT[C/T]TGACAAATGGTAGAT | 51666 |
rs796837161 | snp | C/T | | | intron-variant | ASB4 | GRCh38.p7 | 7:95529937 | TTTATTTAACAAATA[C/T]TTACTTAACACCTCC | 51666 |
rs796910885 | in-del | -/TTC | | | intron-variant | ASB4 | GRCh38.p7 | 7:95515227 | TCTTTCTTTCTTTCT[-/TTC]TTTTTCTTTCTTTCT | 51666 |
rs796924060 | in-del | -/TA | | | utr-variant-3-prime, intron-variant | ASB4 | GRCh38.p7 | 7:95539088 | TTTTTGTTCTTGCTA[-/TA]ATCACTTTTAGATAA | 51666 |
rs796946581 | in-del | -/A | | | intron-variant | ASB4 | GRCh38.p7 | 7:95534341 | ACGTAAAACTCCATT[-/A]AAAAAAAAAAAAGAT | 51666 |
rs796962857 | in-del | -/C | | | intron-variant | ASB4 | GRCh38.p7 | 7:95502390 | ATAGGTACCAGCCTG[-/C]CGGGGGGGGGGCAAA | 51666 |
rs796985670 | in-del | A/GGCCATATG | | | intron-variant | LOC107986823 | GRCh38.p7 | 7:95472231 | ATTCTTTCCCCAAAA[A/GGCCATATG]TGTGTCCAAAATTGA | 51666 |