SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs530909615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923699 | ATTTATAATTTCTTA[C/T]GTATTGCAGGTAGAT | 121441 |
rs530947787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96924444 | ATTCTTTCATGAACA[C/T]GGTATAACTATCTAT | 121441 |
rs530968086 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96910281 | TCTACATTTGGGTAT[G/T]TGTGGATCTGAACTG | 121441 |
rs531020562 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909373 | AGGAGATGACCATGG[C/G]AATCTGGGGAGAACA | 121441 |
rs531173398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922950 | CAAAACCTCATCTCT[A/G]TTAAAAATATAAAGA | 121441 |
rs531209713 | snp | G/T | 0.0178098 | 0.0926698 | upstream-variant-2KB, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96907296 | TGTTGTGTTGCTGCG[G/T]AGAGGTGAGGTTCCG | 121441 |
rs531210348 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96914761 | TTAAAGTAGAATGTA[C/T]CTTTGCCTTGCACCT | 121441 |
rs531277402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909939 | ACACACACACAAACC[A/G]CTTATTAGGTTAAAC | 121441 |
rs531301205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96914094 | AGGCACTCTGTTTAA[C/T]CTGACTTAAGCAGAA | 121441 |
rs531346618 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908151 | TACACATGTTTAAGG[C/T]TCCAAATCCAAACAT | 121441 |
rs531437334 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953684 | TAAAATGTTATATGC[A/C]AAAAATAGGAAACAT | 121441 |
rs531532375 | snp | A/G | 1.66394e-05 | 0.00288434 | missense | NEDD1 | GRCh38.p7 | 12:96940535 | TCTCACCTATCAGAG[A/G]TGGTAAGTCTGTTCA | 121441 |
rs531574325 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96946017 | TCGTACTGCATTTAT[G/T]GATTATGAGCCAGGA | 121441 |
rs531578262 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96938949 | CTTAACCTTTCTGGG[G/T]CTCATTTTTTTCCTG | 121441 |
rs531620326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96939835 | TTCCTCTTTGAAACT[A/G]TGGAGGTTAGTGAAG | 121441 |
rs531932677 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936054 | CTACTATACACACCA[C/G]TAAAGAGCTCAGCTT | 121441 |
rs532031765 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930482 | CTTCCAGGACCAAAT[G/T]GTGACAACATATATG | 121441 |
rs532057851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922463 | ACTGACTTTTCAATA[C/T]CATAAAAATTAGACC | 121441 |
rs532059342 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96927782 | TAATAGTTTTCTCAA[G/T]AATGAATCTATTCTA | 121441 |
rs532065114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96927402 | TGTCTTTCTACAGGG[A/G]AAAAGAGCCTTGCTG | 121441 |
rs532067109 | snp | A/T | 1.77634e-05 | 0.00298017 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936567 | AAGCTAATATACCTG[A/T]ACACACTAACATTTC | 121441 |
rs532071628 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96912542 | TTCCCTGCAGTAGTA[A/G]CAAAGAGAATTAGTC | 121441 |
rs532297296 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96920437 | ACAGCATTACTGTTA[C/T]AGAAATGTGTCACAT | 121441 |
rs532305221 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951206 | AATGGACCTGTAATA[A/G]TTGCATCTACTTGTG | 121441 |
rs532333348 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910054 | GTAATTTACAAAACA[A/G]TATATCATATGAATG | 121441 |
rs532337163 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912661 | TATAATCGCAATTCT[C/T]ATAATAGTCTAGTGC | 121441 |
rs532342679 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913275 | GAGGGGCCTGTCTGA[G/T]CCTCCCCCATACTCT | 121441 |
rs532344291 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96942879 | GAACTGTTTCCAAGC[C/T]CATTCCTATGGCTGT | 121441 |
rs532366342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917839 | ATGATAAAAATAAGA[A/G]GCTTCAGAATTGAAC | 121441 |
rs532376647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910007 | TGAGTAATGTGTTTT[A/G]CATTGCTACCAAGGA | 121441 |
rs532483975 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96949206 | TACCTAGTAGTCTTT[C/G/T]GTTTGCAAGATCATG | 121441 |
rs532507817 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910511 | TCCCTGTCTTGGTGA[A/G]CTCCTCAATGTGGAT | 121441 |
rs532543980 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96918666 | ATCTTTTACCTTTGG[A/G]TCTCTACAGTCGTCT | 121441 |
rs532645306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96949246 | GTCCTGGCTACCTCA[A/G]TGGTTCCCTGATACA | 121441 |
rs532681388 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943119 | CTAGGTCCAAGCCAC[A/G]TTCAAAGGGAGGAGA | 121441 |
rs532765774 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934790 | TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT | 121441 |
rs532776625 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934191 | AAATATAGAAAACAA[A/G]TACAAAATATTATTG | 121441 |
rs532828769 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96950075 | TACCTGCAGTTCTCA[A/T]ATAAATAACAAAGGA | 121441 |
rs532933754 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909316 | GGTCAGGAAAGGCCT[C/T]TCATAGGAGGAAACA | 121441 |
rs532984115 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96932008 | TTGGAACACAGCCAT[A/G]CTTTTCATCTATATA | 121441 |
rs532992558 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96946954 | TCTTTGGGCATTTTG[C/G]TCTTGCCTCTGTAAC | 121441 |
rs533069964 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96948368 | AGTGTTTACTTGGCT[A/T]TTAAAAATCTTATTA | 121441 |
rs533074977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96941378 | TTATAGTCAGAAGGA[A/G]TAAATACATACGTGG | 121441 |
rs533102529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96925645 | CAACATGTACCTATA[C/T]CTCTTCCTCACACCA | 121441 |
rs533109593 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96939782 | TCTTTATTGTTGTCT[A/C]CCTTACTATTCTTTA | 121441 |
rs533112523 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942354 | GCCTCATTAAATGAC[G/T]GTACTATAGAATTAT | 121441 |
rs533112564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96933674 | CTTTTTGTTTTTTTT[C/T]CTTAGCATTTGGTTT | 121441 |
rs533243847 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96924777 | ATGATAAGTTTTTAT[G/T]TCTTATTTCCTAATC | 121441 |
rs533457900 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96931414 | ACAATGTATGAGAGC[A/T]GTTGCAATGTAAGAG | 121441 |
rs533534370 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96914957 | ATGATTGGAGTCCCA[A/G]TATATTGATCTTCAA | 121441 |
rs533544457 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906247 | GCCTCAAGAACTGCA[C/G]ACTGTACAATTAAGG | 121441 |
rs533659453 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952107 | GTTTCTGGCAACACA[A/G]AACTACATAGAATCA | 121441 |
rs533750078 | in-del | -/AT | 0.00318978 | 0.0398085 | intron-variant | NEDD1 | GRCh38.p7 | 12:96933617 | ATTTAATGGGTTAAC[-/AT]ATTAATTGTCTTAAC | 121441 |
rs533775894 | snp | A/C | 1.65564e-05 | 0.00287714 | missense | NEDD1 | GRCh38.p7 | 12:96937381 | GGAACAGTTGCTGTT[A/C]AAGAAAAAGCAGGTA | 121441 |
rs533780313 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96947837 | ACGTTTGGTGAAGAC[G/T]TACAGTCAGTGCCTC | 121441 |
rs533785304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944910 | AATGTTCAAAGAGTT[C/T]AAAGTTTGTGGACAC | 121441 |
rs533813130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937897 | ATGATAAGCTTTCTC[C/T]TATTGTAGAAAATAT | 121441 |
rs533860020 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951578 | TCCATGAAAGGTAAT[A/G]TATTTTAGTTGTTTT | 121441 |
rs534019437 | in-del | -/TTTTTTTTTCCTTAATGTCTTGTA | 0.084364 | 0.187256 | intron-variant | NEDD1 | GRCh38.p7 | 12:96929357 | CTTAATGTCTTGTAT[-/TTTTTTTTTCCTTAATGTCTTGTA]TTTTTTTTTTCTTTC | 121441 |
rs534110196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96929922 | CATGCTTTTCTGTGA[A/G]TACCTTTTGGCTGTT | 121441 |
rs534201786 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96918475 | TTAATCCATCTCCCA[C/T]GTAAGCTTCACTTAC | 121441 |
rs534214553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96919930 | TACAGAAACATGAAA[A/G]TGGGCTGTTCGAGGA | 121441 |
rs534232594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943344 | GGAGATGGATATCAT[C/T]ATTTACATTTGTAGA | 121441 |
rs534270541 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NEDD1 | GRCh38.p7 | 12:96924378 | ATTTTGATTAAGATT[A/G]TATTGGATCTATGGA | 121441 |
rs534304539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936348 | AAGAAATAGGTGCTG[C/T]TTCTATAAGATGCAG | 121441 |
rs534357651 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96927814 | ATTGGTTTATTTCAT[G/T]GACTGGTTATATTTA | 121441 |
rs534567062 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934593 | CCCAGGCTGGAGTAC[A/T]ATAGTGTGATCTTGG | 121441 |
rs534706481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96925933 | GAGAGCACTAGGAGT[A/G]AAGCACCTTAGCTAG | 121441 |
rs534738500 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96918097 | TTGTTTTGTGATGAT[A/T]GTATTCAATACAGTA | 121441 |
rs534773918 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910231 | GTTGGTAGTTGTGGA[A/T]ATAATTCCAAAAGGT | 121441 |
rs534802232 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96947385 | TTATTTTATACTGAT[A/G]TGTGTGGGAACAGCT | 121441 |
rs534887723 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96948932 | TTCCTGCCATCTAAC[C/T]CAGGGGGAGCATTGC | 121441 |
rs534926191 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96949513 | TTGAATGCAATTCCA[A/G/T]TTAAAATCCCAGCTG | 121441 |
rs534927630 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940994 | TGATAAATAGAAGCA[A/T]TATTTGTTATTCTTC | 121441 |
rs534931850 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96947776 | CTTTCTGTGCCTCAG[C/G]AGAAGTGTGTCTGTC | 121441 |
rs534982757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908667 | CAAGTATTGGTATAG[A/G]GACTTAGTGGCGTCT | 121441 |
rs535014168 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96913430 | CCAGGCTGGAGTGCA[A/G]TGGTGCAATCTTAGC | 121441 |
rs535151301 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96943449 | AAACCAGTCTTCAGA[A/G]TGCAGATCCATATCT | 121441 |
rs535224402 | in-del | -/TA | 0.00318978 | 0.0398085 | intron-variant | NEDD1 | GRCh38.p7 | 12:96939796 | TACCTTACTATTCTT[-/TA]TGAGTTTGGTGTTCT | 121441 |
rs535345326 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD1 | GRCh38.p7 | 12:96919753 | AGAGGAAGTGAATTC[C/T]TTAAGGAAGACATAA | 121441 |
rs535381590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923854 | TGCCTGTTTGCGTGT[A/G]TGTGTGTGTTTTAGT | 121441 |
rs535389427 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96915254 | AATCTATTTGATTTC[C/T]TTGAAGCATTTTTGA | 121441 |
rs535504981 | snp | A/C | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953582 | ATAATGTATATTAAA[A/C]GAGGTGGGATGAAAT | 121441 |
rs535524090 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96946182 | AGTATGTTCATAGAT[C/G]TATTAGGTATGCTGT | 121441 |
rs535525371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937769 | CTTATGATTTGATCT[C/T]ATTAAATAAAAATAA | 121441 |
rs535568029 | snp | A/G | | | intron-variant, synonymous-codon, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96924912 | TGGAAGAAGCATTCA[A/G]TTTACTACCAAGCAT | 121441 |
rs535803474 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96919862 | ATTCTCTGTATATTT[G/T]AGGAAAATGTTAAAG | 121441 |
rs535809814 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NEDD1 | GRCh38.p7 | 12:96907442 | GAGCGGTTGCTGGGC[G/T]GGGGCGCGGCGGCGC | 121441 |
rs535823135 | in-del | -/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96947195 | CTGTTATTTTTAATA[-/C]ACAGTGTTAAAGAAT | 121441 |
rs535896841 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928656 | GGTCATTATGTATTG[C/T]TATTGTTAGGTACAT | 121441 |
rs535935357 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96921128 | TGACAATATAAACTG[A/G]CCTCTTTGCCAATTA | 121441 |
rs535950350 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96950640 | TGCACAATGAAAACA[A/T]TGACTACAGATTATA | 121441 |
rs535974787 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96921703 | CTTACTCTATTGCCT[A/G]TGCTGGAGTGCAGGG | 121441 |
rs536016262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913614 | CCTGACCTCATGATC[C/T]GCCCGCCTCAGCCTC | 121441 |
rs536162172 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953013 | AGAAAGGTTGTCAAA[A/G]TAAGTTATACCTCTT | 121441 |
rs536293347 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96944312 | ATCTTTTGATTTATT[G/T]TGCAAATATTATTGA | 121441 |
rs536340804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96911700 | TTTTCTATATTCTAA[A/G]GAGAAAAGTAGTGGT | 121441 |
rs536370605 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96949123 | GCCACTGCTTCAGCT[C/G/T]GGTTTCTTCTCCACA | 121441 |
rs536440248 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96918257 | AATGTTTCTTTAATA[A/G]TTAGCTTTTTGTAGT | 121441 |
rs536524798 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96939652 | TGAACCTCTAAAACT[A/G]TCGTTACTCCAGTAA | 121441 |
rs536531802 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96926960 | CTGCTGCACTCCAGC[A/C]TGGGTGACAGAGCGA | 121441 |
rs536561943 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96924482 | AGCCTTTAATTTTTC[C/T]TAGCAGTGCTTTGTT | 121441 |
rs536567028 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96918968 | ATACTTGAAGGACCA[C/G]TTGAAAAAGTTGTAA | 121441 |
rs536755822 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943300 | CAAAGTATTTTCACA[A/T]ATAATATCTTTGAAG | 121441 |
rs536808331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917466 | CATGTGGAAGAAAGA[C/T]GATGAGAGAGTGGCT | 121441 |
rs536897012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935491 | ATAAAATGCATATGT[C/T]TTTAACCCAAATGAT | 121441 |
rs536900548 | in-del | -/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96934054 | ATGGATATAGTCCAT[-/C]CCCAGTCTAGAGTGT | 121441 |
rs537080131 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96919365 | ATGTACTTCATTTAT[A/G]AAATGGGCAAAATGA | 121441 |
rs537089899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932952 | GTTTGCTGAGCGTCC[A/G]CTGAACTTAGGTTTA | 121441 |
rs537128474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96933776 | TAGAATATAAATTCA[C/T]AGGGAAAAATTAGCT | 121441 |
rs537147685 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96915137 | GCAACTATACTGAAA[C/T]ATTGATGTTGTGTGC | 121441 |
rs537178256 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96938017 | ACAAATACTTTAGAA[A/G]GTCTACATGGTATAC | 121441 |
rs537238752 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | NEDD1 | GRCh38.p7 | 12:96954001 | CATCTTTAAAGTACT[A/G]AAAGAAAAGTTCAAT | 121441 |
rs537312305 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96947161 | TGAGTGCTTTGCCCT[A/C]ATCCTTTTTCCCTAA | 121441 |
rs537351378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917969 | ACAACTTTTTTCTTG[C/T]TTTTTATTTAGTTCT | 121441 |
rs537353578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940910 | ATTTAAAAAATTGTG[C/T]GTGTATAGGTGTACA | 121441 |
rs537383864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910090 | TGATTTTATCTGTTG[C/T]GTTCATTTAAAAAAA | 121441 |
rs537413606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96914440 | TCTTTCCCATAGTTA[A/G]CAAATTGTATCATAA | 121441 |
rs537435655 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96908692 | GCGTCTCATTTGACC[A/G]TATTGCTAATTTTAG | 121441 |
rs537444992 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96940683 | TGGTATCTTTTTCTT[C/T]GCCCTGATATTTCAA | 121441 |
rs537622643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908949 | TGGGAGGCTGAGGCG[A/G]GCAGATCACCTGAGG | 121441 |
rs537679997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96946400 | ATATTTTTGGAAGCT[A/G]TCTTCAATTATTAAA | 121441 |
rs537729270 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96948351 | ATTCTAAACTATCAA[A/G]CAGTGTTTACTTGGC | 121441 |
rs537773670 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922732 | TAAATACATTGGTGT[A/T]ACTACTAACAAAATC | 121441 |
rs537829053 | snp | A/G | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953388 | CATTTGTACTGAAGC[A/G]TATAGGGATGTTAAT | 121441 |
rs537904800 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952849 | TGGAGATTTCATATT[A/G]GGTACTAAATATTAT | 121441 |
rs537911387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945010 | GATCTTTTGGTGTGA[A/G]TTAGATTTTCAGTGT | 121441 |
rs537956585 | snp | A/G | 0.000150299 | 0.00866759 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96951996 | AGTGAATGAAGGTTT[A/G]GTGGCTGAAATTGAA | 121441 |
rs537965772 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96950864 | TATTATACTTAATAA[C/T]TTTTACATATTCTTT | 121441 |
rs538154210 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96921600 | AATAAATATTTGAAT[A/G]TATGAATATTTTTAG | 121441 |
rs538190827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913546 | GCCTGGCTAATTTTT[A/G]TATTTTTAGTAGAGA | 121441 |
rs538328400 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937137 | AGGGAATTTATAAAA[C/T]ATTAATGTATAGTAT | 121441 |
rs538330247 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96927977 | TGTAGTATTGGTATA[C/T]ACTTGACTAGCCTAT | 121441 |
rs538366965 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928567 | AAGTCACTAGTTTTT[C/T]ATTCCTAGGTTATTC | 121441 |
rs538397030 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96921005 | ATAAAACAGTCTTAT[A/G]GTGATTCAGAACAGC | 121441 |
rs538484637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96949669 | AATTATTAAAGTATA[A/G]TTAAGATATATAGCA | 121441 |
rs538493242 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96924491 | TTTTTCTTAGCAGTG[C/G]TTTGTTTTTACTGTA | 121441 |
rs538521913 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943404 | TTTTGCCCAAAAATA[C/T]ACATCAATTGCGGGG | 121441 |
rs538527770 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913012 | AGGTAAAATAGTTTT[G/T]AATATAGGGGAACAA | 121441 |
rs538570848 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96908370 | GACTCGGGGACCTGC[C/T]TGTGACATCACTAAT | 121441 |
rs538580146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96926858 | CAGGTGTGGTGGTGC[A/G]CGCCTATAGTCCTAG | 121441 |
rs538700542 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96914097 | CACTCTGTTTAACCT[G/T]ACTTAAGCAGAATCA | 121441 |
rs538716503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96918924 | CCTTGGTTTTGGGAA[A/G]GGAATAATAGGTAAA | 121441 |
rs538760642 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96918139 | GTCAGCTTTTTAGTT[A/G]TGTAGTATATTTGGC | 121441 |
rs538765743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910698 | GTGACAACCCAAAAC[A/G]TTTCCAGAATTGCCT | 121441 |
rs538871090 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96949015 | TTCTGCAGGCCTCCT[C/G]TCTTCAAGACCTTGG | 121441 |
rs538876937 | snp | A/G | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905363 | CTTCATATATTTCAA[A/G]ATTCTCTTACGTTCA | 121441 |
rs538887282 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96937898 | TGATAAGCTTTCTCT[C/T]ATTGTAGAAAATATT | 121441 |
rs538890427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96950309 | AGCAAGAAGAACTCT[A/G]TTATACTGGTGACAT | 121441 |
rs538894027 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96933927 | TTATTCAAACTAGAT[C/G]TTTGTTTATTCTGGT | 121441 |
rs538933738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934683 | GCTGTAATTACAGGC[A/G]CCTGCCACCATGCCC | 121441 |
rs538972537 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96941085 | TTTTTCTTAGTGGAA[A/T]GGAGTTACCTCATTG | 121441 |
rs539138247 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96911061 | AGTAAAACAAATTAC[-/T]TTGGTACTCTGTTAA | 121441 |
rs539193370 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96931899 | GGTTTTTCTTCTTTG[A/T]GATAAAAAAAATTTT | 121441 |
rs539211587 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923999 | TTCTGTGTTTTCTTT[A/T]AGAAGCTTTGTTGTT | 121441 |
rs539341709 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NEDD1 | GRCh38.p7 | 12:96916582 | CCTACAAAGGACATG[A/G]ACTCATCATTTTTTA | 121441 |
rs539402979 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930763 | GCCAAGGACCAACCC[G/T]GAGTGTGGGACTTTT | 121441 |
rs539477563 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940118 | TTAGAAAAATTCCAA[C/G]AAAATGGCTAAAATA | 121441 |
rs539494255 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96928483 | ATTTCCTTTAAGGAG[A/C]TTAAGTGTTACCCTA | 121441 |
rs539516803 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940826 | CATAGGCAATCTGTC[C/T]CTTGTATCTACTTCT | 121441 |
rs539516813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96931967 | CTATAACCTATGGTC[C/T]AGCCAACTTATTTTT | 121441 |
rs539534386 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923404 | TTGCAGGATTGTAGC[A/G]TAGGCATACAGTTTT | 121441 |
rs539719160 | snp | G/T | 0.000798403 | 0.0199641 | downstream-variant-500B | NEDD1 | GRCh38.p7 | 12:96953850 | GAACCTCAAACACAA[G/T]AAATAAAAAGAAAAC | 121441 |
rs539878799 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943499 | TATCATGTTAAATGC[C/T]TTTCTTCAATGTCCA | 121441 |
rs539883724 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96950879 | TTTTTACATATTCTT[C/T]TGTAGGCATGAATTA | 121441 |
rs539904573 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935975 | AATTTTTACTGTTAG[C/G]ACTTATTTGCTGTCT | 121441 |
rs539937492 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96942814 | TATCTTCCTGCTTCA[A/G]TCAGGATGTCAACCA | 121441 |
rs539940654 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936506 | TGTGCTCTTTGACCA[G/T]TTTGAAGTGTTAATA | 121441 |
rs539965261 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96914333 | GGGAGCTTTTTTTTT[A/T]AAGTATAAAAATAAC | 121441 |
rs540002388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912326 | TAGTTTAGATTGTTA[C/T]CAAGCACTAGGTTAA | 121441 |
rs540007723 | snp | A/G | 0.000103514 | 0.0071935 | utr-variant-5-prime, intron-variant | NEDD1 | GRCh38.p7 | 12:96907579 | TCTCCTTTTTTGTCA[A/G]CCTCAAGTACTTTTC | 121441 |
rs540222630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96950033 | ACTATTTATCACACA[A/G]TATCACAGAGTGAAG | 121441 |
rs540306679 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96925546 | TTGCATATCTAGCTC[A/G]GGAGCAGCTGAATAT | 121441 |
rs540341290 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96918556 | CAATTACTCTGGATG[A/G]TTTTCTGTCTTTTCG | 121441 |
rs540378439 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96919083 | ATATGGCATCTTCCT[C/G]TTAAAAACTCTTCTC | 121441 |
rs540384247 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910401 | TATCTTCCTTCCTCT[C/G]TGTGTGTGTGATGAA | 121441 |
rs540459086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928189 | TATAGTTATACTCAT[C/T]CTGTTTGTCCAATCA | 121441 |
rs540518085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910936 | GTGACTGGTTCAGGA[A/G]CAAAAATATTAAAAG | 121441 |
rs540544592 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930633 | AAATTAGGTGTTCAG[C/T]TGTGGTTCAGCCTTA | 121441 |
rs540548035 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912613 | TACTCTGTAAGCTAT[A/T]CTCATTGCTTGTCTT | 121441 |
rs540970517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934236 | CCCAGTATTCCCTTA[C/T]ACTTGTTGATTTGAC | 121441 |
rs540981942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96916808 | TTAAAGTCCACCCTA[C/T]TTATGAAGGATGGAA | 121441 |
rs541099704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96946446 | TTTCCTTTCTAACCT[A/G]TAGTTAATGTTGTAG | 121441 |
rs541116603 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909242 | AAATCAGGTATTGGG[A/G]TATAGGGTAAACTGC | 121441 |
rs541130473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940267 | TTAACTTTAGCTCTT[A/G]TCATATTCTGTTTTA | 121441 |
rs541274880 | snp | C/T | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906084 | ATTTTCCTGCTGGCT[C/T]CAATTTTCAGAGATT | 121441 |
rs541342860 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942762 | CTGTGTATTAAGAAC[G/T]GAGCATGACTTGGCT | 121441 |
rs541407688 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936353 | ATAGGTGCTGCTTCT[A/G]TAAGATGCAGAATGT | 121441 |
rs541501800 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96938153 | TAGCATGATTTTGCT[A/G]TTTCCAAGTAGAAGC | 121441 |
rs541578332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913858 | CTTAAATTATTATGA[A/G]TTGTCATAATTTTAC | 121441 |
rs541625622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96938337 | CAAAGACAACTGATA[C/T]CTACTTAAGGAAGAA | 121441 |
rs541690330 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932985 | TGAAGGGAACATTTA[A/T]CATTATCTTTAGCCT | 121441 |
rs541713969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96914553 | GTTTTTTAGCTTTTA[C/T]TAGTAATGTTTACAG | 121441 |
rs541738396 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96917207 | TGTACACTGGAAATT[A/C]TTTTAAAGTCTCTTC | 121441 |
rs541785279 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96907928 | TAAATCACCCGGCGA[A/G]TTGTGTTTCCTAAGT | 121441 |
rs541851436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96929058 | TTTCTTAAATTATAA[C/T]TTTTAGTATTCTTTT | 121441 |
rs541988407 | in-del | -/T | 0.010558 | 0.0718854 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937430 | TGGAGGGTTGGTTTG[-/T]TTTTTTTTTTGTTTT | 121441 |
rs542152009 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96948481 | AGAGGAACTCCTCAT[G/T]TTCTGGATTTTAGTT | 121441 |
rs542224163 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96909304 | GTTAGCCAGGGTGGT[C/G]AGGAAAGGCCTTTCA | 121441 |
rs542283624 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96949941 | GGAAATCATTAAAAA[A/T]AAAATAATGCACTGC | 121441 |
rs542357391 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96927143 | TGAGAAAAATGGTAA[A/G]TAGGGCACATCCATG | 121441 |
rs542402725 | in-del | -/TTTAT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96939467 | GTGTTATTAGAAAAG[-/TTTAT]TTTATTCGCCAGTCT | 121441 |
rs542475061 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951746 | AGCATTTTAAATGTG[C/G]AAATATAAATTTTCC | 121441 |
rs542514698 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937489 | CATTCTTCAAGAACA[C/T]AGAACTCAAATTTAT | 121441 |
rs542548036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945053 | TAATATGGTAGAGAT[A/G]GAATTATTATGTAGG | 121441 |
rs542713779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943439 | TCTGAGAAACAAACC[A/G]GTCTTCAGAATGCAG | 121441 |
rs542721285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96925462 | AAACAGATTCCAGGA[C/T]TTTCAGATCATACAA | 121441 |
rs542923396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96927236 | AATGATCAAATTAGT[A/G]TCTTAGTGAAAGTGA | 121441 |
rs542946153 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96915626 | TGCACTGTGGAAGTT[C/T]CAACTAATGTGACTT | 121441 |
rs542960069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96919473 | CAGTTTCTGTTATCT[C/T]ACAGATGCCTTGCTC | 121441 |
rs543037403 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96948094 | AGGACCTCTTTCTCA[A/G]CCATCCTCCCGTGGC | 121441 |
rs543040461 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEDD1 | GRCh38.p7 | 12:96941935 | ATATTTCTCCTGATA[C/T]AGTTGTGTGTTTATT | 121441 |
rs543133838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96915420 | TAAAGAATCTCTTTT[A/G]AGCAGAGGATATTTC | 121441 |
rs543378331 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96946732 | TTTCTCTTAATGTGA[A/T]TTAATTCATTTGGGA | 121441 |
rs543565630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909206 | AAAATTCAGATATTA[A/G]GAAGTGCTATGAAAA | 121441 |
rs543647309 | snp | G/T | 2.94252e-05 | 0.00383559 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945892 | TCTAGACCTTACTTG[G/T]TTTTTTTTTAGATGT | 121441 |
rs543688017 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96939419 | CTTCAACAATAGTAC[A/C]AATGATTTGGTAATA | 121441 |
rs543691503 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96950272 | ATAAAAAATCTGGTA[A/C]TACTAAGTCTTGATG | 121441 |
rs543910775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928849 | CTGCTACCACGCCTG[A/G]CTAATTTTTTGTAGT | 121441 |
rs543963175 | snp | C/T | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905894 | GTGTTTTTAGAAAGA[C/T]GAAATTATATATATA | 121441 |
rs544038300 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934090 | GTTTTTCCTTTGTGG[A/T]TTAATTTTTTTTTAA | 121441 |
rs544049565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930112 | TTGTAAATGTTGTCC[A/G]TGGGATTTTAGTTTT | 121441 |
rs544098843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96931016 | AGGATGGATAGTAAG[C/T]CACTGAGAATGGAAA | 121441 |
rs544128918 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96913374 | ACTGTTGCCTTATCC[-/T]TTTTTTTTTTTTCTT | 121441 |
rs544204756 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96923250 | TATGAATGGGCCACC[A/T]TTTATCCATTCTTTT | 121441 |
rs544205026 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913755 | CACTCTTTGAAAGCT[A/C]TTTCTTTTTTAAATA | 121441 |
rs544328895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96918677 | TTGGATCTCTACAGT[C/T]GTCTCCCTGGTGATT | 121441 |
rs544401880 | snp | A/G | 1.65441e-05 | 0.00287607 | missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96920078 | ATTATTTTACACAGT[A/G]TAACCACTAATTTAT | 121441 |
rs544424171 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96944933 | GTGGACACTTCTGTT[G/T]TGTGAGTGTTACTAA | 121441 |
rs544439520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96911814 | ATCATAATAAAATTA[C/T]AGTCTATGCTCTGTT | 121441 |
rs544439773 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96921308 | TGTCTCAGTCTCCCA[A/C]GTAACTGGGATTACA | 121441 |
rs544476705 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913291 | CCTCCCCCATACTCT[C/T]CTTAAACAGGTTGGC | 121441 |
rs544496724 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96950104 | GATCAGATTATGTAA[A/C]GAATGCTTATAAATG | 121441 |
rs544555623 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910323 | CAGAACTTGAAGGCA[A/G]AAGCAAGTTGGGGAG | 121441 |
rs544631938 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96928844 | GGCGCCTGCTACCAC[A/G]CCTGGCTAATTTTTT | 121441 |
rs544665061 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96927198 | TTGCTTCTATGAACA[A/C]TCACAAATTTCAAAT | 121441 |
rs544715909 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96911009 | ACAAATTTTCTTACT[G/T]AATTAAATTTACCTC | 121441 |
rs545019444 | in-del | -/TT | 0.499946 | 0.00519141 | intron-variant | NEDD1 | GRCh38.p7 | 12:96921662 | GCTTTAGAAGAGGGA[-/TT]TTTTTTTTTTTCTTT | 121441 |
rs545072679 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932333 | ATTTGGAGGCCAGGT[A/G]CGGTGGCTCACACCT | 121441 |
rs545153857 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96926909 | AGAGGAGAGATTGAG[C/T]CTGGGAGGTTGAGGC | 121441 |
rs545215619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942800 | TTTGCCTTCAAGTCT[A/G]TCTTCCTGCTTCAAT | 121441 |
rs545260891 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96939282 | CGCTGTTTTCAAATG[A/T]TACCAAACTTCTGTT | 121441 |
rs545296201 | snp | A/G | 8.23879e-05 | 0.00641772 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96935113 | ACACAAAGCTCCAGC[A/G]TCAGGCATCTGTTTT | 121441 |
rs545333327 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96926511 | GATTTTACATACTTA[C/T]GTTTTCCTTTTATGG | 121441 |
rs545404186 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909047 | CGGGTGTGGTGGTGC[A/C/T]TGCCGGTAATCCCAG | 121441 |
rs545411260 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96947484 | CCTGAGGGACAGTTG[G/T]GAAGGTCTTAACACA | 121441 |
rs545489197 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96907913 | GCCGAAAACAAACAT[C/T]AAATCACCCGGCGAG | 121441 |
rs545508779 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96914621 | CAAGTCCTCTTACTC[C/G]TGTATTATTTGAGGC | 121441 |
rs545547477 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908013 | CACTACACCCCGCAG[C/T]TCACCAGGCCTGGTT | 121441 |
rs545669214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96925304 | AGGATTTGGAGAGCA[C/T]TGTAAGCAGAGGTTA | 121441 |
rs545669546 | in-del | -/A | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96925809 | TATCTAAGATCAGAT[-/A]AAACTAGAACTTGAG | 121441 |
rs545684531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908789 | AAAAATTAGGAAGTT[A/G]CTTATTAGTAGTTAT | 121441 |
rs545706158 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96926012 | ATCTTTCAAGTGAGA[A/T]TAATATACTTTCAAA | 121441 |
rs545736373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909320 | AGGAAAGGCCTTTCA[C/T]AGGAGGAAACATTTG | 121441 |
rs545830893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922453 | TAAATTTTGGACTGA[C/T]TTTTCAATACCATAA | 121441 |
rs545935103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96915360 | TTATAGTATTTGAAC[A/G]TGCAATGGGGGAAGG | 121441 |
rs546069054 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952429 | TTTCAAATTTTTGGG[A/G]CTAGTTGAGATTTAA | 121441 |
rs546104196 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96923079 | TTCTGATTGTGCCAC[G/T]GCACTCCAGCCTCAG | 121441 |
rs546176606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943097 | TACTTTTGTTAGAAG[C/T]AAGTTACTAGGTCCA | 121441 |
rs546226677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935359 | AGAATTTTCTTCTTA[C/T]GCAGAAAGAAATAGA | 121441 |
rs546230180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951783 | ACTAATTTCACCAAC[A/G]ATCTTCCATTTATAT | 121441 |
rs546282538 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930111 | GTTGTAAATGTTGTC[C/T]GTGGGATTTTAGTTT | 121441 |
rs546350024 | snp | A/G | 0 | 0 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906999 | CACAGTAAACAGCAA[A/G]TGAATGACAAGCAGT | 121441 |
rs546444178 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945081 | AGGACCCTTTGAAAA[A/G]GGTTGGTTAACTACC | 121441 |
rs546487875 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930321 | TCACAGGATTCTGTA[C/T]ATAGTCATACTCATG | 121441 |
rs546494962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96938253 | CCTGTGAATATCTGT[A/G]TCATCCTTATATAAG | 121441 |
rs546517788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96919566 | CTCTTTTCTCTAAGG[C/T]TGAACTCCAGCTTTA | 121441 |
rs546519657 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96939232 | TTAGTTTTAGAAGGA[A/T]ATCACCATTTAAGAA | 121441 |
rs546618138 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96937834 | CTCTCATGTAATTGG[C/T]GAAACAGTTCTGAAA | 121441 |
rs546629331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917323 | AGGATGGGCAAACAA[A/G]CCCTGATGGGAGACC | 121441 |
rs546668287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909595 | ATGCGACCTGGCTTA[C/T]GTTTTAGGAAAATCA | 121441 |
rs546707075 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909970 | AACCACTGTCAATGA[A/C]ACTTTTGCATGTGCC | 121441 |
rs546727549 | snp | A/C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96945539 | ATAGAAAGTTTCTAA[A/C/G]ATTTGTATTCCAGAC | 121441 |
rs546749522 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913452 | AATCTTAGCTCACTG[C/T]AACCTCCGCCTCCCC | 121441 |
rs546802783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96948581 | TTTGTTTTCGTTATT[A/G]GAGTTGAGAAATTAT | 121441 |
rs546894982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96911361 | TAGCTATGAGATAGT[A/G]TTGTATGACTTTTGG | 121441 |
rs546928940 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96949187 | CAGAGGTAAATGAAG[A/G]GCTTACCTAGTAGTC | 121441 |
rs546933975 | snp | A/G | 0.0118316 | 0.0759986 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942667 | GAAAATGAAAAGTGA[A/G]TTGTATTATCTATGC | 121441 |
rs547053805 | snp | C/G | 0.000798403 | 0.0199641 | downstream-variant-500B | NEDD1 | GRCh38.p7 | 12:96953821 | AGAAACAAATGAGAC[C/G]TAAGAAACTCAATGA | 121441 |
rs547100606 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96931356 | TTCTGACAAAAAGCA[A/G]GGCAAAAATTCACAA | 121441 |
rs547308939 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96913104 | GATCTCTGTTGCTGC[C/T]ATTTTAGGACGATAT | 121441 |
rs547338849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923873 | GTGTGTTTTAGTGAA[C/T]AGAAGTTCTTAAATT | 121441 |
rs547385167 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945248 | ACAATCAACTCTCAT[A/T]TAAATATCTATATTT | 121441 |
rs547500674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96938847 | CTCTCACACACACAC[A/G]CATTTTTCTTTGCCT | 121441 |
rs547540428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930689 | AGGCAGAGTGAGTGA[A/G]CCACTCTTACGAGTT | 121441 |
rs547638718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96941327 | CAATTTCATTTTTTA[C/T]TTTAAAATTGTCTCT | 121441 |
rs547759024 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937877 | AGACTTTATTGATGT[C/G]TTATATGATAAGCTT | 121441 |
rs547824668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96920587 | TATATGATAAAGTAT[C/T]GAAGCTTATATATTT | 121441 |
rs548031148 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906730 | AGCCTGAGCGCGTTT[C/T]CTGGCTTGTAAATCG | 121441 |
rs548041847 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944895 | TAATCATAGACTAAA[A/T]ATGTTCAAAGAGTTT | 121441 |
rs548048534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96914271 | CTACCACTATATATA[C/T]GTACTACTGTTATGC | 121441 |
rs548055485 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96934457 | CTGAATGACACCGTG[G/T]TTGTCATGATTGAAA | 121441 |
rs548100853 | in-del | -/AA/AAA | 0.0892964 | 0.192297 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935834 | CTAAAAAACAAAAAC[-/AA/AAA]AAAAACAAAAGAATG | 121441 |
rs548269633 | snp | C/T | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906591 | TCCACCTTGAAGTAT[C/T]CCCTTCAAAAGAATT | 121441 |
rs548278526 | snp | A/C | 0.00199481 | 0.0315187 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906005 | TAACTAGTATTATAT[A/C]ATATAATATGTATAT | 121441 |
rs548488602 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96913297 | CCATACTCTCCTTAA[A/G]CAGGTTGGCTTTGTC | 121441 |
rs548521324 | snp | G/T | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952736 | TAAAAAATGTTTAAG[G/T]TTCATAGGACTCGAC | 121441 |
rs548548787 | in-del | -/A | 3.32588e-05 | 0.00407778 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917748 | TAAGGTAAGCAATTT[-/A]AAAAAAAATCTTCAT | 121441 |
rs548564243 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96948540 | TCGGTTGAATTTAAA[A/T]TAATATGATTTTATA | 121441 |
rs548567108 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936882 | ATATGGAAATTATAT[A/G]TGGTCAATTAAACAG | 121441 |
rs548605878 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928449 | GTTCTCTTTCAATGT[A/G]ATTTAGTAGCAGGCT | 121441 |
rs548625662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96949434 | TTTTTTTGTTTAAAA[A/G]CATTAACATTTAAAT | 121441 |
rs548662781 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NEDD1 | GRCh38.p7 | 12:96950256 | GAGTAAATGGGAAAA[C/T]ATAAAAAATCTGGTA | 121441 |
rs548789358 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96921925 | CCAGCTGGGAGAGGG[A/G]TGTTTTACATGGAGG | 121441 |
rs548810330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935258 | ATAGCTATTATTCCA[C/T]TAACAGGCATATTTG | 121441 |
rs548828168 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96927502 | CATCTTAGGCTCACA[A/C]ATAGGTTAACTTGTG | 121441 |
rs549069706 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96940788 | AATTTCCACAAAAGT[C/T]TCTTGAAGGAAGTTT | 121441 |
rs549105224 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96925767 | ATCTTTTAGTTTAGG[A/C]AAACAGTAATGCTCA | 121441 |
rs549224351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96947744 | AGCTTGTTTTTCACT[A/G]TCTAACCTGTTCCTG | 121441 |
rs549224824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908966 | CAGATCACCTGAGGT[C/T]AGGAGTTCGAGACCA | 121441 |
rs549242069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917989 | TATTTAGTTCTACTC[C/T]TATTTGAATGAACCA | 121441 |
rs549242286 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96926621 | TCTGATTGTGGCCCA[A/G]AGCATCGAATTGCTA | 121441 |
rs549382547 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96943269 | TACTGACTAAAACAT[C/T]GTGTTTTGCTGTTTT | 121441 |
rs549447581 | in-del | -/TG | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96923788 | TCCTTAATACCTGTT[-/TG]TGTGTGTGTGTGTGT | 121441 |
rs549464686 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917165 | ACTTCTTTAAAAAAA[A/C]ACTTATCCCATCGGT | 121441 |
rs549601203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909415 | GGGAGCAGCAAATGA[A/G]AAGACACTGAGGTGA | 121441 |
rs549632636 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96931662 | CAAATGTCTAACATG[A/G]TATTATTTAGGTAAA | 121441 |
rs549667450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923298 | TGTCTTGTTTTAGCT[A/G]TTACAAGGTAGCTAC | 121441 |
rs549704721 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96946019 | GTACTGCATTTATTG[A/C]TTATGAGCCAGGAAA | 121441 |
rs549707481 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953478 | TCACTAACAGGTTTA[G/T]AAGACATAAATATTA | 121441 |
rs549805819 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945628 | CATGCCAAATCTTAT[G/T]TAGAAATGTTTGATG | 121441 |
rs549822904 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952906 | AATAAGAAGCTTGGA[C/T]TATTTTATTTTGTGG | 121441 |
rs549925865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944869 | ATTTAACTTGTAAAG[A/G]AGAAATAGAGTAATC | 121441 |
rs549964529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937650 | TCTTAAAAATGGAAG[A/G]AGGCTAACTCAGAAA | 121441 |
rs549981376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96946764 | CAGTAGAATAGAACA[C/T]TGTTGACAATATGAT | 121441 |
rs550143926 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944326 | TTTGCAAATATTATT[C/G]ACTGGTTACCACATG | 121441 |
rs550155648 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96926895 | AGGAGGCTGAGGTGA[G/T]AGGAGAGATTGAGCC | 121441 |
rs550155745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936152 | TAGCTTTTTGGCCAA[A/G]ACTGTACAACTAAGA | 121441 |
rs550180642 | snp | G/T | 0.000158149 | 0.00889097 | missense | NEDD1 | GRCh38.p7 | 12:96937202 | TTACATTTCAGTCAA[G/T]TTTAAATAAAGGCTG | 121441 |
rs550271596 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96927543 | CAAGCTGCAGCCTTT[C/T]CCAAAGCAATTACAA | 121441 |
rs550343503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96938420 | TATATTATGAAAATT[A/G]TCTTTTTTCAAAATT | 121441 |
rs550393252 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96929464 | GTGTGGGATATATCT[A/G]TGAAATTAGTTTTAG | 121441 |
rs550410365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96920438 | CAGCATTACTGTTAT[A/G]GAAATGTGTCACATA | 121441 |
rs550421108 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913574 | AGACGGGGTTTCACC[A/G]TGTTGGCCAGGCTGG | 121441 |
rs550430301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96921632 | GATGACAAAGATTTT[A/G]TTAGGCAAATATAAA | 121441 |
rs550472921 | in-del | -/AGAG | 0.00835141 | 0.0640778 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935418 | CTGAAACATGAACAT[-/AGAG]AGATGACATCTTAAT | 121441 |
rs550476461 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96927897 | AGTGGTCTTTTTTAT[A/G]TTATATAGGAGCATT | 121441 |
rs550557758 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96937662 | AAGGAGGCTAACTCA[G/T]AAATTATTCATCCTT | 121441 |
rs550604237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910030 | ACCAAGGATAGATAA[C/T]GTAAAATAGTAATTT | 121441 |
rs550706437 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96921083 | GGGAGTTTCAGCTAC[A/G]TCTAAGGCTTATTGA | 121441 |
rs550779205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910524 | GAGCTCCTCAATGTG[A/G]ATAAAATAAAATGAG | 121441 |
rs550793067 | in-del | -/AA | 0.00597247 | 0.0543191 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932862 | TTGTGTCAGGAAAAC[-/AA]GAGTGTTTTCTATTA | 121441 |
rs550801194 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96912602 | TTTTTGAAAGCTACT[A/C]TGTAAGCTATACTCA | 121441 |
rs550874068 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96940190 | AACCTTTTGTTCCAT[A/G]AAAATCCTGGTTAAC | 121441 |
rs550882272 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905936 | CACATTACGTCTATA[C/T]ACACAAATACAGTGC | 121441 |
rs550919137 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906588 | TTTTCCACCTTGAAG[C/T]ATCCCCTTCAAAAGA | 121441 |
rs550954958 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922921 | GGAGTTCAAGACCAC[-/CT]TGGGCAATGTGGCAA | 121441 |
rs551043350 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96932076 | TCCCCCCACCTTTAG[C/T]GAGTGGTATGTTTTT | 121441 |
rs551069473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96946982 | AACTTGATAGCCGCA[A/G]TCCTTCTATCCTCTT | 121441 |
rs551104647 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96934830 | GGCGTGAGCCACCAC[A/G]TCTGGCTGAAACCTG | 121441 |
rs551169075 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936222 | TCATGAGGCCTAAGC[A/G]GGTCAATAAATGGAA | 121441 |
rs551253434 | in-del | -/T/TT | 0.0509478 | 0.151255 | intron-variant | NEDD1 | GRCh38.p7 | 12:96926031 | ATACTTTCAAAGGGA[-/T/TT]TTTTTTTTTTTGATG | 121441 |
rs551318933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96924825 | TTTTTCTTTATTGCG[C/T]TGACTAGGCTCTCCA | 121441 |
rs551358872 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96939790 | GTTGTCTACCTTACT[A/G]TTCTTTATGAGTTTG | 121441 |
rs551374379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96947687 | AGCAACTCTGAAATC[A/G]CTGTGCATTTCTGCC | 121441 |
rs551397527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96931445 | CAGTTGCAAATTAGT[A/G]TTTTAAAAATCTTCA | 121441 |
rs551468669 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96914741 | TGATTTTGTATTTCA[A/C]CTCTTTAAAGTAGAA | 121441 |
rs551839424 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906822 | GCATCTTATACCTTT[A/C]ATTATCATAGTTTCA | 121441 |
rs551865263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923663 | CATTTTTATGTTGGG[C/T]TATTCGTGTTTTTAA | 121441 |
rs551874467 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96907270 | CCAGCGCGGAGCCGG[C/T]CGCGGCCCCCTGTTG | 121441 |
rs552000020 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96915942 | TACATTAGGTAGCCA[A/G]TGGAGGTCCCTTGAA | 121441 |
rs552150689 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96920455 | AAATGTGTCACATAG[C/T]TCAGATTTTGTCAGC | 121441 |
rs552291325 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952147 | TCATGGCCTCCAGGG[A/G]AAAAATGTTTTTCAA | 121441 |
rs552304084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951166 | ACAAGTTATATCTAC[C/T]CTGGTTAAGTTATTT | 121441 |
rs552401657 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945972 | GTAATCCTAAAGCCA[G/T]AGAAAACATAATGAG | 121441 |
rs552517682 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96919391 | AATGACCTTGCCCCT[C/G]AGGCTTTTCTAAGCA | 121441 |
rs552605060 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96921548 | CTTTGTCCTCAGTCT[A/G]TTTTCTAGTTTCTTG | 121441 |
rs552619262 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943819 | ATCAGTAGAAAGTGG[G/T]TGGCTGCCAGTGCAT | 121441 |
rs552655996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944295 | GTAAGAAGTACAAAA[A/G]CATCTTTTGATTTAT | 121441 |
rs552729253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96925968 | GTGAACTTGAACAAG[C/T]TACTTAACTCTCAAG | 121441 |
rs552771670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928484 | TTTCCTTTAAGGAGC[C/T]TAAGTGTTACCCTAT | 121441 |
rs552810410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96920949 | TTTCATATATATTGG[A/G]GAATAATACAGATAT | 121441 |
rs552840120 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937571 | ATAGTAACTTTGGCT[A/G]TTAATTTCAAAAATG | 121441 |
rs552875444 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96923900 | AATTTAATGAAGTCT[C/T]ATATGTCAGTCTTTT | 121441 |
rs553031800 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96949601 | AAGAATAACTAAGAC[A/G]TTTCAGAGAAGAATA | 121441 |
rs553040236 | snp | A/T | 0.000575819 | 0.0169581 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917614 | TTTTTTTTTTTTTTT[A/T]AAATAGCAAAAGCAG | 121441 |
rs553090419 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NEDD1 | GRCh38.p7 | 12:96947422 | GAGACATGATCATAC[A/G]TTCTAGGAATGTTTG | 121441 |
rs553112222 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910232 | TTGGTAGTTGTGGAA[A/C]TAATTCCAAAAGGTT | 121441 |
rs553137009 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96948937 | GCCATCTAACCCAGG[C/G]GGAGCATTGCTTAGA | 121441 |
rs553158963 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96925613 | ACACTATTTTCTTGT[C/T]TCTTTGTGCAGGAGT | 121441 |
rs553174295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96941577 | GAGAAAAGTGACTAG[C/T]GCTGGAGTTGAGAAA | 121441 |
rs553408876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910684 | AATAGCCTCTAGTTG[C/T]GACAACCCAAAACGT | 121441 |
rs553497587 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906538 | ATAAAAGGACCTTTG[A/G]AAGGGGCACTTGAAA | 121441 |
rs553549168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930898 | TCTGCCACCACCATA[A/G]CCAGTAACTTCTCAG | 121441 |
rs553653381 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908704 | ACCATATTGCTAATT[G/T]TAGAGTTTTGGAAAA | 121441 |
rs553699745 | snp | C/T | | | downstream-variant-500B | NEDD1 | GRCh38.p7 | 12:96953997 | GCAACATCTTTAAAG[C/T]ACTGAAAGAAAAGTT | 121441 |
rs553778907 | snp | C/T | 4.99721e-05 | 0.00499836 | missense | NEDD1 | GRCh38.p7 | 12:96945702 | TTTTAGATCCAAAGA[C/T]AGCATCTTCTGTCAC | 121441 |
rs553827874 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | NEDD1 | GRCh38.p7 | 12:96939190 | TTCAGTTATTTCAAA[C/G]AACTTCTCTAAACTT | 121441 |
rs553869200 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928737 | TGTCACCCAGGCTGG[A/G]GTGCAGTGGCACTGT | 121441 |
rs553884703 | in-del | -/GTTAA | 0.00318978 | 0.0398085 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951170 | GTTATATCTACTCTG[-/GTTAA]GTTATTTCTTTTGTA | 121441 |
rs553930788 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96931910 | TTTGTGATAAAAAAA[A/T]TTTTTTTCTATTAAA | 121441 |
rs553945005 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96922882 | CACTTTGGGAGGCTG[A/C]GGCAGGCAGATCCCT | 121441 |
rs554073057 | snp | A/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952352 | AAAATTGTGCATAAA[A/T]ATTGGTTATGTTTGT | 121441 |
rs554272932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913136 | CCACATAGGTTACTA[A/G]GTTGACCTGAGCATA | 121441 |
rs554273047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96921717 | TATGCTGGAGTGCAG[A/G]GGAATGATCATGGCT | 121441 |
rs554309763 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913618 | ACCTCATGATCCGCC[C/T]GCCTCAGCCTCCCAA | 121441 |
rs554348995 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905255 | GATTTGTTTTTCTTA[C/T]CTGGATGTTCTATGA | 121441 |
rs554487058 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953071 | CTACTATGATCTACA[A/G]TTTTAGGTTAAGTGA | 121441 |
rs554515136 | snp | A/G | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952393 | TCTTTTTTAACATAT[A/G]TTTTTGATTGACAAA | 121441 |
rs554523893 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96949293 | TCAATACAGTTTTTA[A/C]TATAATTGAAAGTAG | 121441 |
rs554564588 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944392 | TATTTTAAATGATAC[G/T]TAACAGCAGGTGCTT | 121441 |
rs554642796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942006 | TCATTTTTAATTCAC[C/T]TGTTAAATTTGAATT | 121441 |
rs554762873 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936484 | TTAAACAAATATTTG[G/T]GATATGTGTGCTCTT | 121441 |
rs554770532 | snp | A/G | 0.0952156 | 0.196321 | intron-variant | NEDD1 | GRCh38.p7 | 12:96926994 | AAAAAAAAATTGTGT[A/G]TGTGTGTGTGTGTGT | 121441 |
rs554844217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96919881 | AAAATGTTAAAGCAA[A/G]TATTAGATTGATAAA | 121441 |
rs554853571 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935504 | GTTTTTAACCCAAAT[G/T]ATTAATTTGCTTTAA | 121441 |
rs554962000 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96947211 | ACAGTGTTAAAGAAT[A/G]TACGTTTTTTTCAGG | 121441 |
rs554971853 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942739 | AAACATTTATCGTCT[C/G]ATAATTTCTGTGTAT | 121441 |
rs555098651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96933796 | AAAAATTAGCTTAAA[C/T]GTAAAGTACTTAATT | 121441 |
rs555170355 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909220 | AGGAAGTGCTATGAA[A/G]AAAATGAAATCAGGT | 121441 |
rs555241505 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96929021 | ATATGTAGTTTCAAG[G/T]CTTTTTTTATTTTTG | 121441 |
rs555244444 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910914 | AAAAAAATCAAAGCT[C/T]TAAAATGTGACTGGT | 121441 |
rs555332247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932960 | AGCGTCCACTGAACT[C/T]AGGTTTATCTGAAGG | 121441 |
rs555349728 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910150 | CACTGCTATTAAAAA[A/C]AGTATATTCTGTCTA | 121441 |
rs555469758 | snp | A/G | 0 | 0 | intron-variant, missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96924899 | TGTCCCCAAATTCTG[A/G]AAGAAGCATTCAATT | 121441 |
rs555517111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96907688 | GATTGAAAGTTGGAG[A/G]ACTTTCATTTCAGCT | 121441 |
rs555575064 | snp | C/G | 1.65274e-05 | 0.00287462 | missense, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96909811 | GATATTAAAATATGG[C/G]ATGCTTCATCTATGA | 121441 |
rs555602247 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96928856 | CACGCCTGGCTAATT[C/T]TTTGTAGTTTTTGTA | 121441 |
rs555696751 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940208 | AATCCTGGTTAACTT[C/T]AGCTCTTGTCATATT | 121441 |
rs555719022 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96936041 | CCATTCTTCTTTTCT[A/G]CTATACACACCAGTA | 121441 |
rs555746870 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96948214 | ATCTGTATCTTAGGG[A/T]GTCTCCCTCAGCCCT | 121441 |
rs555773783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96915224 | GGAACCCTGGGGTCC[A/G]CAGAAGTGAACACAA | 121441 |
rs555820167 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96910499 | TGATTGACACCTTCC[C/T]TGTCTTGGTGAGCTC | 121441 |
rs555827019 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96938129 | AAATATTTATTGGTG[-/T]TTTTTTTTTAGCATG | 121441 |
rs555908461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945050 | CTTTAATATGGTAGA[A/G]ATAGAATTATTATGT | 121441 |
rs555932035 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930181 | CACACACACACACAC[A/T]CACACACACACACAC | 121441 |
rs555936955 | snp | A/G | 0.000188129 | 0.00969686 | intron-variant | NEDD1 | GRCh38.p7 | 12:96924800 | TCCTAATCTTTATAT[A/G]TGTTATTACTTTTTC | 121441 |
rs555969026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930849 | GCACACACACGTACA[C/T]ATGCACTCACAGTAT | 121441 |
rs555978823 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940936 | GTACACCTCCCACCA[C/G]CCCATAAAAAAGTTG | 121441 |
rs555980640 | in-del | -/A/AA | 0.475789 | 0.107327 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909176 | GTGAAACTCCGTCTC[-/A/AA]AAAAAAAAAAAAAAA | 121441 |
rs556190516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96914449 | TAGTTAACAAATTGT[A/G]TCATAATGCTGTTGG | 121441 |
rs556216741 | snp | A/G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96924824 | CTTTTTCTTTATTGC[A/G/T]TTGACTAGGCTCTCC | 121441 |
rs556416794 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906362 | AAAATGCACTTATTA[C/G]AATTTTCCAATTATC | 121441 |
rs556586746 | snp | G/T | 1.72862e-05 | 0.00293987 | intron-variant | NEDD1 | GRCh38.p7 | 12:96920156 | ATTCAGAGTAAAATT[G/T]GTAAGATAGATTTTG | 121441 |
rs556623330 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912112 | GGTAAATAAAATTAC[A/G]TTTTATTTAAAAATT | 121441 |
rs556626028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928120 | CTTCAGTAGAAAGCT[A/G]TTTGAAAGATGTTTT | 121441 |
rs556699532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96921021 | GTGATTCAGAACAGC[C/T]GAGAGAAGACTATCT | 121441 |
rs556716523 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96918943 | ATAATAGGTAAAGAA[A/C]TCTCTGAAAATACTT | 121441 |
rs556751475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910756 | TGTGACCACAGTGCT[C/T]CTATCACCTTTTATG | 121441 |
rs556913642 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96918334 | TTTGGAATTCTACTT[C/T]TCATTATATTGTCTT | 121441 |
rs556944893 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951675 | CCTCCTTTTTAACCT[C/G]TGAGATACTTAAGCC | 121441 |
rs556952439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910265 | GGAATGAGTTTTTGC[A/G]TCTACATTTGGGTAT | 121441 |
rs556973881 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96921181 | ATTACTCTTTTTTTG[C/G]TTGTTTGTTTGGTTT | 121441 |
rs557061354 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96947509 | AACACACAGGTAATG[C/G]AGAGCCATCAGAGTT | 121441 |
rs557091202 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96910974 | TGACTTACTATTCTT[C/G]CATGTATATAACAAG | 121441 |
rs557139867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943411 | CAAAAATACACATCA[A/G]TTGCGGGGTGTATCT | 121441 |
rs557152220 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96914780 | TGCCTTGCACCTTGA[A/G]CAGTTCAGGATTCCT | 121441 |
rs557246983 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935840 | AAACAAAAACAAAAA[C/G]AAAAGAATGCAAGAG | 121441 |
rs557249566 | snp | C/T | 3.31279e-05 | 0.00406975 | missense | NEDD1 | GRCh38.p7 | 12:96945720 | CATCTTCTGTCACTG[C/T]TGGAGTTGCCAGTTC | 121441 |
rs557273605 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96908513 | ATCGTTCATTACTAC[C/T]TGTTGCTCTTTAAAG | 121441 |
rs557343690 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96947956 | GCCTCTGCCTGGGAC[A/G]CAGTGAAGACCCAGA | 121441 |
rs557604402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909172 | CAAGAGTGAAACTCC[A/G]TCTCAAAAAAAAAAA | 121441 |
rs557805976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932023 | GCTTTTCATCTATAT[A/G]TTGTCTGTAACTACT | 121441 |
rs557845035 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932917 | GGAGAGTTTAAGTAA[A/T]TCACCTAAATCATAC | 121441 |
rs557926612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96924141 | CCAACCTATCCCCAC[C/T]GAATTACATTAATGC | 121441 |
rs557940185 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96920539 | GTGTTTAGGCAGAGA[A/G]TAATTTAAGTTTTGC | 121441 |
rs557964848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96916598 | ACTCATCATTTTTTA[C/T]GGCTGCATAGTATTC | 121441 |
rs558075187 | snp | A/G | 0.000544721 | 0.0164944 | missense | NEDD1 | GRCh38.p7 | 12:96945828 | TTCAGAACATGATAC[A/G]GGAAACGTTGGATGA | 121441 |
rs558141877 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96935760 | ACTGGTGTACATAAT[C/G]CTCTAAGCATTTGGG | 121441 |
rs558215293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913702 | TAAGTTAATCCCTCT[A/G]ATTAAGGATAATACT | 121441 |
rs558258147 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96907034 | AGTGGCCGGAGCTCC[A/G]TCGCTGGGGCGTGGA | 121441 |
rs558271644 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951593 | ATATTTTAGTTGTTT[A/T]GTTTAGTTTCTAAGA | 121441 |
rs558290780 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant | NEDD1 | GRCh38.p7 | 12:96907605 | TTTTCTTTTGGCAGG[G/T]ACTTGGATGCATTTT | 121441 |
rs558495810 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96950998 | TAATAAAATGATCTT[C/T]CTAACCTAGTGAATT | 121441 |
rs558538908 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96918553 | TCTCAATTACTCTGG[A/G]TGGTTTTCTGTCTTT | 121441 |
rs558543914 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96947877 | CTGCCCTGTGCTGCA[A/T]GTCTGCACCTAGGAG | 121441 |
rs558594564 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930549 | TGCCCAGGGTTTTTA[-/T]TTGGGGGGGCTGGTT | 121441 |
rs558603928 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96950742 | TTCTTGGGCTTTTTC[C/T]CAAGAGTTAAGTGAT | 121441 |
rs558737313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928783 | GCTCCGCCTCCTGGG[C/T]TCACACCATTCTCCT | 121441 |
rs558770334 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96949541 | CTGGGATTTGGAAGA[A/G]GATGATGAAGTGATT | 121441 |
rs558799430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96911792 | AATGATTTGATTTGC[A/G]TCATGTATCATAATA | 121441 |
rs558834683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912949 | TTAAGCTCAAAATAA[C/T]ATAGTAACACTTAAA | 121441 |
rs558923528 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96919933 | AGAAACATGAAAATG[A/G]GCTGTTCGAGGATTA | 121441 |
rs558970084 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943354 | ATCATCATTTACATT[G/T]GTAGATCGGGAAATA | 121441 |
rs559014945 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935731 | AGCACCCACTTGAGA[A/C]ATACTGATTATGTAC | 121441 |
rs559035651 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96927879 | AAAGACTTTTTATCT[A/G]GAAGTGGTCTTTTTT | 121441 |
rs559098631 | snp | C/T | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906357 | CTGAAAAAATGCACT[C/T]ATTAGAATTTTCCAA | 121441 |
rs559106373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96919133 | TCTCCTGCTGGACAT[C/T]TCTAATTTGATGTTG | 121441 |
rs559324250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96946522 | AGTTTTTGTTGGTGC[A/G]TGCTTCCTTTTAATG | 121441 |
rs559385035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908897 | AATTTCAGATAGTGG[C/T]TGGGCACGGTGGCTC | 121441 |
rs559389253 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96916842 | AGGAGAGCAGGAGTG[A/G]AAACAGGGAAACCAG | 121441 |
rs559467781 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940357 | CAACCTAGCTTATGA[A/T]AAAATTTATTTAGAT | 121441 |
rs559573668 | in-del | -/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96923946 | TTTTTGTGTTCTCTT[-/G]GAAGAATCTTGCCTG | 121441 |
rs559596622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942313 | ACCTACCCCCTACAC[C/T]AGGGCTTGTTACACT | 121441 |
rs559713761 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908974 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC | 121441 |
rs559741486 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96921482 | CACTGCACCCAGCCA[G/T]GGTTAGTCTTTTTCA | 121441 |
rs559757651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96924295 | TTCACTTTGACTACT[A/G]TGGGCCTTTTGCATT | 121441 |
rs559776474 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922396 | TTTAAGGACATAGAG[A/T]AACTTTCTTTTTTTG | 121441 |
rs559878405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96929154 | CAAGTGTTTTTAAAC[C/T]TTTTTGTTATTTCTT | 121441 |
rs559883681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932200 | CGGGATTTTTTCCCC[C/T]CCATAAGCTTCTTGA | 121441 |
rs559920628 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923616 | TATATTTTTATATGC[C/T]TCTTGTGAAGTGACT | 121441 |
rs559949736 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96914597 | TGCTAATAACCTTTT[G/T]GTAACTTCCAAGTCC | 121441 |
rs560042988 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96919784 | TGCCATGTAGAAAAT[A/T]ACCTGTCCATAATCT | 121441 |
rs560118468 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930300 | TTGGTCATTCTCTAG[A/G]AGAACTCACAGGATT | 121441 |
rs560122709 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96907201 | CCCCGTGACGTCACT[A/C]GGGGCGGGACTTCCG | 121441 |
rs560179489 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952745 | TTTAAGGTTCATAGG[A/C]CTCGACAAGAGCTAT | 121441 |
rs560279035 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96933044 | ATGTAGGTCCCAAGA[A/C]CTTGAAGTAAGATAC | 121441 |
rs560350267 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905766 | TTTGCAGTCTCATGG[G/T]CCCAGGTTTAACTTC | 121441 |
rs560367012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96907962 | AGCAGGTCGTTTGAA[C/T]CCAGTTTTTCTGAGC | 121441 |
rs560374897 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96927186 | ATTTTTCTACTTTTG[C/T]TTCTATGAACAATCA | 121441 |
rs560455720 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930632 | GAAATTAGGTGTTCA[G/T]CTGTGGTTCAGCCTT | 121441 |
rs560553437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96949951 | AAAAATAAAATAATG[C/T]ACTGCCTATAAAAAT | 121441 |
rs560594708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951125 | TTACATCCTAGCTCC[A/G]TCATTTACTGGTTGT | 121441 |
rs560634044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951763 | AATATAAATTTTCCA[A/G]ATATACTAATTTCAC | 121441 |
rs560639260 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906404 | TGCAGATAACTGGGG[C/T]TGATGTACCTAGTTC | 121441 |
rs560674594 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96942033 | AATTTTACAATTTTT[A/G]TTATGGACTGGCAAA | 121441 |
rs560687572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943485 | CATGTTAATCTGCCT[A/G]TCATGTTAAATGCTT | 121441 |
rs560704586 | snp | A/G | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953048 | AATAGATAGATGTAT[A/G]CATCTACCTACTATG | 121441 |
rs560950095 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96927281 | CTCACAGAATCTGCA[A/T]CATACTGAATTGTAT | 121441 |
rs560955765 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NEDD1 | GRCh38.p7 | 12:96929647 | TTAATGGCTGCTTGC[C/T]TTCTGGGGTTCCCTG | 121441 |
rs560961863 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96924517 | CTGTAGAGGGCTTGC[A/G]TATCTTTTAGTAGAT | 121441 |
rs560999455 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96925504 | CTATTTTACATATCA[C/G]CTCTTCAGAAGTGGT | 121441 |
rs561028865 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96939489 | TATTCGCCAGTCTTG[G/T]GCATTTTTGGATATG | 121441 |
rs561123518 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96926651 | ACTTAATGAATGTTT[A/G]TTAATTAAAAAAAGT | 121441 |
rs561127851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96919484 | ATCTCACAGATGCCT[C/T]GCTCATTTGTTTTTC | 121441 |
rs561138701 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934103 | GGTTTAATTTTTTTT[A/T]AAATTATGCTTCAGG | 121441 |
rs561272841 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96948546 | GAATTTAAAATAATA[C/T]GATTTTATAGGTTAT | 121441 |
rs561290931 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96912662 | ATAATCGCAATTCTT[A/C]TAATAGTCTAGTGCT | 121441 |
rs561310714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96933329 | TGAAGGACGATAACT[A/G]TATGAACTCCTAAAG | 121441 |
rs561558474 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909963 | GTTAAACAACCACTG[A/T]CAATGAAACTTTTGC | 121441 |
rs561559018 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908235 | TGAATGGAGCATAAG[G/T]AAGCACATGAGTGAA | 121441 |
rs561656840 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923594 | GTCCATGTTGAATGA[A/T]GTTAAGTATATTTTT | 121441 |
rs561720998 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952577 | TGAAGTCAAGTATGA[C/G]TATTATTTATTGTAC | 121441 |
rs561746239 | snp | A/G | 8.41347e-05 | 0.00648539 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940571 | TCCTGTTCTCTTGCT[A/G]GTAGTTAATATTTTT | 121441 |
rs561748988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96915594 | AATGTCTCCTTTGAA[C/T]TTGAAGAATCCAAGG | 121441 |
rs561875842 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96947609 | TCACCACTGGCTTCA[G/T]ATGATTTGAGGACAG | 121441 |
rs561893738 | snp | G/T | 0.000101504 | 0.00712332 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945897 | ACCTTACTTGTTTTT[G/T]TTTTAGATGTAAAAC | 121441 |
rs562052581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96941298 | AAGTTGTTTCATCCA[C/T]TCATTATCTTATACA | 121441 |
rs562281599 | in-del | -/T | 0.499776 | 0.0105807 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934207 | ACAAAATATTATTGC[-/T]TTTTTTTTTTTCTCC | 121441 |
rs562283703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96931044 | AAATGGGATAACTAT[A/G]TAGTGGCTTAGGTGA | 121441 |
rs562319158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923132 | AAAAGAAAAAAAAAA[A/G]CAAGGAATCATATGT | 121441 |
rs562322841 | snp | A/C | 1.65072e-05 | 0.00287286 | stop-gained | NEDD1 | GRCh38.p7 | 12:96936736 | TAAGAATGTTGAAAT[A/C]ACCAGTTAAGACCAT | 121441 |
rs562326278 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96931820 | ACATACACACAGAAA[A/C]ATACTTAAAGGATAC | 121441 |
rs562335231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96921354 | GCCCAGCTAATTTTT[A/G]TATTTTAGTAGAGAT | 121441 |
rs562478778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951896 | ATTAAACATAGCCTG[C/T]CAAATAAATGTGAAA | 121441 |
rs562568976 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96918905 | CCTCAAGATAGCAAG[G/T]GTTCCTTGGTTTTGG | 121441 |
rs562576864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96927068 | CAAATCTGTCAAAAA[A/G]TTGACATAATTGAAT | 121441 |
rs562708116 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96917490 | AGTGGCTCTTTAGTA[C/G]AAGATTAGCATGTTT | 121441 |
rs562769086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913764 | AAAGCTATTTCTTTT[C/T]TAAATAAGATAAGAT | 121441 |
rs562803458 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96907143 | GACCCTCTGTACCCC[A/G]ACTTCTGTCCGGCCA | 121441 |
rs562808342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96911198 | TTTAGATTTTCATTA[C/T]GTTTAGAGCTTAATT | 121441 |
rs562851165 | snp | C/G | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952620 | AATTTTTGGAATTTT[C/G]AATTGCACAAATTAC | 121441 |
rs562861696 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96927231 | TTAAAAATGATCAAA[C/T]TAGTGTCTTAGTGAA | 121441 |
rs562895360 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96918678 | TGGATCTCTACAGTC[A/G]TCTCCCTGGTGATTA | 121441 |
rs562976448 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96939345 | AAACATGTTAAGGAC[C/T]TAGAAAAAAGGAGAG | 121441 |
rs563044224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96950231 | ATGCAATGAGATACC[A/G]TGTCACACCGAGTAA | 121441 |
rs563084455 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96921473 | GGTATGAGCCACTGC[A/T]CCCAGCCAGGGTTAG | 121441 |
rs563304351 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96948524 | TTTCCATTCTCAGCT[C/G]TCGGTTGAATTTAAA | 121441 |
rs563360500 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932410 | CCAGGAGTTTGAGAC[A/C]AGCCTGGGCAAAATG | 121441 |
rs563439035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942429 | TAAAAGAGAAATTTA[A/G]ATCAGTATTCTCCTA | 121441 |
rs563531768 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96924432 | TTAACAATATTGATT[C/T]TTTCATGAACATGGT | 121441 |
rs563549887 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96941165 | AGAGTTAATATATTC[A/G]TACTTTTTGGCCTTG | 121441 |
rs563631728 | in-del | -/T | 0.488242 | 0.0757679 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917600 | TAAATTAAGGTAACT[-/T]TTTTTTTTTTTTTTA | 121441 |
rs563796289 | snp | A/G/T | 8.26625e-05 | 0.0064285 | missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96917727 | CAAAAAGAGTTCATC[A/G/T]ATCTCTTAAGGTAAG | 121441 |
rs563909409 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922460 | TGGACTGACTTTTCA[A/T]TACCATAAAAATTAG | 121441 |
rs563937350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909343 | AACATTTGAGCTAAG[A/G]CCTGAATGATGAGAA | 121441 |
rs563948022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96914052 | TGGGACAGAGGGAAC[A/G]TGTGCTAACAGTAGA | 121441 |
rs563975738 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908800 | AGTTACTTATTAGTA[C/G]TTATTTGTTGTGAAA | 121441 |
rs564053996 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930981 | CAGGTTTGAAGATGT[C/T]AGTTACTGCAACAGA | 121441 |
rs564097975 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953661 | AAAAGCTAAGTAAGT[A/G]TAAAAAATAAAATGT | 121441 |
rs564130100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922925 | TTCAAGACCACCTTG[A/G]GCAATGTGGCAAAAC | 121441 |
rs564134698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96946004 | TTTGTTGATCTTTTC[A/G]TACTGCATTTATTGA | 121441 |
rs564450710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96946740 | AATGTGAATTAATTC[A/G]TTTGGGATCAGTAGA | 121441 |
rs564485982 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96912620 | TAAGCTATACTCATT[G/T]CTTGTCTTCTTAGTG | 121441 |
rs564509654 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906450 | GTAGTTGTGATGAAA[A/G]AATAACACTTTTTGC | 121441 |
rs564545210 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935981 | TACTGTTAGGACTTA[C/T]TTGCTGTCTTCTTTT | 121441 |
rs564568132 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96933771 | TTAAGTAGAATATAA[A/G]TTCATAGGGAAAAAT | 121441 |
rs564647478 | snp | A/C | 0.00159617 | 0.0282053 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952445 | CTAGTTGAGATTTAA[A/C]GAGTTTGATATGCCT | 121441 |
rs564718607 | in-del | -/A | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96910898 | ATTCTACTTTCTGAT[-/A]AAAAAAATCAAAGCT | 121441 |
rs564912566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928281 | AACCATAATTTTTAA[C/T]GACTGGATGTATTTC | 121441 |
rs564953943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96920410 | ATGTAAAAAATGGAT[A/G]TTAATCTTTCTACAG | 121441 |
rs564963553 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96944593 | ATATGGGTAATATGA[A/G]TAAAAAAATTGTATA | 121441 |
rs565036170 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96927358 | ATGTCTGAGCTGAAT[G/T]AAAGTTATTAGCTTT | 121441 |
rs565038337 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96936240 | TCAATAAATGGAAAG[C/T]GGATACTTAGGCCCT | 121441 |
rs565043876 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96939804 | TATTCTTTATGAGTT[C/T]GGTGTTCTGGTTTGC | 121441 |
rs565108620 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96908928 | ACGCCTGTGGTCCCA[A/G]CACTTTGGGAGGCTG | 121441 |
rs565138135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910477 | TTTTCTAAGCTTTTT[A/G]TGTTTCTGATTGACA | 121441 |
rs565143896 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96921243 | CTAGAGTATAGTGGC[A/C/G]CAATCTCAGCTCACT | 121441 |
rs565174857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910948 | GGAACAAAAATATTA[A/G]AAGTTTTATATGACT | 121441 |
rs565190671 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NEDD1 | GRCh38.p7 | 12:96918583 | TTCGGTGTGAAATTC[A/G]TAATGTTTAGCTCCC | 121441 |
rs565301450 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917837 | TTATGATAAAAATAA[C/G]AGGCTTCAGAATTGA | 121441 |
rs565634698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96946232 | AAAGATACTTTAAAG[C/T]ACAATTCTGAATGTT | 121441 |
rs565636276 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96931476 | TAGCCCAATAGAAAA[C/T]AGGCAAAGTAGAATA | 121441 |
rs565682664 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96916546 | TTACTGAGAATGATG[A/G]TTTCCAATTTCATCC | 121441 |
rs565707312 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96938858 | ACACACATTTTTCTT[A/T]GCCTCTGAAACATTG | 121441 |
rs565743069 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96933668 | TAACTCCTTTTTGTT[A/T]TTTTTTCTTAGCATT | 121441 |
rs565773069 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NEDD1 | GRCh38.p7 | 12:96946826 | CCAAAATAAAGTACA[A/C]CTGAACACAGCTGAA | 121441 |
rs565812055 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940742 | AATTTTCACATGGGA[A/T]TTATGCAAATAGCTC | 121441 |
rs565878504 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96924761 | TGGCTGTCATCTGTG[A/C]ATGATAAGTTTTTAT | 121441 |
rs565987058 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935724 | ACCTGGGAGCACCCA[C/T]TTGAGAAATACTGAT | 121441 |
rs566118385 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96911754 | GGAAATGGTTTTTCT[C/G]GCTATGGTAATATCT | 121441 |
rs566124920 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923177 | AGTCATCATTACATT[C/T]GCTTTGTTGCATGGA | 121441 |
rs566155126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912896 | TATTGTGGTGCTTGC[A/G]ACTAAATATAAAGGT | 121441 |
rs566258624 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96914330 | TTTGGGAGCTTTTTT[G/T]TTAAAGTATAAAAAT | 121441 |
rs566286479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944488 | TGCCTCCAGTTCTCT[C/T]TTTCTTTTTCTTCTT | 121441 |
rs566295471 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96914896 | GTTAGCCAGCTCTAA[A/G]TATAATTTTTATTTT | 121441 |
rs566301511 | snp | C/T | 0.000103557 | 0.00719499 | utr-variant-5-prime, intron-variant | NEDD1 | GRCh38.p7 | 12:96907568 | CCACAAGTCTGTCTC[C/T]TTTTTTGTCAACCTC | 121441 |
rs566333955 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908333 | TGGCTTATACTAGAC[A/G/T]TAGGTGTGCTGTTGT | 121441 |
rs566403054 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906038 | TATATTACATGTATT[A/C]TTATATATATTTTCA | 121441 |
rs566421074 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944904 | ACTAAAAATGTTCAA[A/C]GAGTTTAAAGTTTGT | 121441 |
rs566462520 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951563 | GTGAATTTTTAAAAA[A/T]CCATGAAAGGTAATA | 121441 |
rs566647059 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96944986 | CGTTAAATTCAGGTA[C/T]GTTGATTTGATCTTT | 121441 |
rs566726891 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913484 | GTTCAAGCGATTCTC[C/T]TGCCTCAGCCTCTCA | 121441 |
rs566826414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96949472 | GAGATTATAAAGATA[C/T]TAGTTCACCTAAATA | 121441 |
rs566871799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96919919 | TGTATGGTATTTACA[A/G]AAACATGAAAATGGG | 121441 |
rs566917586 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96921998 | CTTTATATAGGACCA[A/G]TGTGAGAAAAGATTG | 121441 |
rs566962632 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96950262 | ATGGGAAAATATAAA[A/C]AATCTGGTAATACTA | 121441 |
rs566999415 | snp | A/G | 0.000265041 | 0.0115087 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943794 | GATACTGAACTCACT[A/G]TATGTGTTTATCAGT | 121441 |
rs567055359 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96950361 | AAACAATTTGCATGA[C/T]TTTGTAAAAGTATAC | 121441 |
rs567064295 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937023 | TTATATATCTCTCTT[A/T]TTAAAAGTATTTTAA | 121441 |
rs567082805 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96923554 | GTTATGTAGTGCTGT[C/T]TCATGGTGGTTTTAA | 121441 |
rs567225444 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NEDD1 | GRCh38.p7 | 12:96933816 | AGTACTTAATTTTCC[A/G]CCTAGTAAATGACAA | 121441 |
rs567269068 | in-del | -/GTGA | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944935 | GGACACTTCTGTTGT[-/GTGA]GTGTTACTAAAGACA | 121441 |
rs567277672 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937996 | ATGCTATACTGTCAA[C/T]GTGCAACAAATACTT | 121441 |
rs567307949 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923844 | TGAAACTGTATGCCT[C/G]TTTGCGTGTGTGTGT | 121441 |
rs567333724 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96938716 | CAGAAAAGTTTTAAG[A/C]ATAGTACAGATAACT | 121441 |
rs567345293 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NEDD1 | GRCh38.p7 | 12:96916170 | GCCCAAATAATAGGA[C/G]TTTGAAAGCCAGGTA | 121441 |
rs567417938 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96935433 | AGAGAGATGACATCT[G/T]AATGATTTCACATTT | 121441 |
rs567473564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96947356 | CAGATTTAGAAAGGT[A/G]CACTGAAGAGATTTT | 121441 |
rs567474520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910154 | GCTATTAAAAAAAGT[A/G]TATTCTGTCTACACC | 121441 |
rs567609371 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922409 | AGTAACTTTCTTTTT[G/T]TGTGTGTGTTAGAAG | 121441 |
rs567618235 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96910519 | TTGGTGAGCTCCTCA[A/G]TGTGGATAAAATAAA | 121441 |
rs567904433 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96916053 | AGAATAGCTGTGTAG[-/A]AAGCCTTGAGGCAAA | 121441 |
rs568012329 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953007 | TTATTTAGAAAGGTT[A/G]TCAAAATAAGTTATA | 121441 |
rs568024702 | snp | A/T | | | intron-variant, synonymous-codon, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96924900 | GTCCCCAAATTCTGG[A/T]AGAAGCATTCAATTT | 121441 |
rs568039870 | snp | G/T | 0.00953873 | 0.0683987 | upstream-variant-2KB, intron-variant | NEDD1 | GRCh38.p7 | 12:96907362 | TCCGCGCACCCTCCC[G/T]ATCCTAAGACCCGCT | 121441 |
rs568062986 | in-del | -/T | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953558 | GCTTTTTTAAAAAAA[-/T]AAATACACATAATGT | 121441 |
rs568149761 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NEDD1 | GRCh38.p7 | 12:96953776 | AAAAAAGAAAATATG[C/T]GAAACAGTTGTCAGA | 121441 |
rs568188370 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96946142 | GGACAAGTTCTGGTA[A/C]GCTTAAATTGGGTTC | 121441 |
rs568313468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932768 | CAATGATGAGCAAGT[A/G]AGTTATGAACTTCTG | 121441 |
rs568441684 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937706 | ACTGAATGGCTTTTC[A/T]TTGTGTCTTCAGATT | 121441 |
rs568524969 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96919809 | TAATCTCTCTCTCTC[A/G]TAAAGTGCCTGGACC | 121441 |
rs568615129 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906950 | CAGGCTAAACCATCA[C/T]TGTACACTCAAGAGT | 121441 |
rs568685253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922587 | TCCTGAAAACATTAG[A/G]TTTGACTATACCTTT | 121441 |
rs568810507 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96911689 | TCAGTCCTTTTTTTT[C/G]TATATTCTAAGGAGA | 121441 |
rs568812179 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96918945 | AATAGGTAAAGAAAT[C/G]TCTGAAAATACTTGA | 121441 |
rs569020990 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96921242 | GCTAGAGTATAGTGG[C/T]GCAATCTCAGCTCAC | 121441 |
rs569021434 | snp | C/G | 8.24273e-05 | 0.00641926 | missense, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96912778 | AGTTGTCTCAAGTTG[C/G]AAATGTAAACCTGTT | 121441 |
rs569045175 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96912957 | AAAATAATATAGTAA[C/T]ACTTAAAAATGAGAT | 121441 |
rs569247802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96926926 | TGGGAGGTTGAGGCT[A/G]CAGTGAGCCATGACT | 121441 |
rs569316546 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96946509 | GGAGAAAATGTGCAG[-/T]TTTTGTTGGTGCATG | 121441 |
rs569326464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943267 | AATACTGACTAAAAC[A/G]TTGTGTTTTGCTGTT | 121441 |
rs569371310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942718 | CACTTTGAGGCTTAA[A/G]AAAATAAACATTTAT | 121441 |
rs569411002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96949400 | GTAGTGAAGATTTTT[A/G]TAGAAAAACATTAAA | 121441 |
rs569417332 | in-del | -/TTG | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96929090 | CTCTCTTTGGATTTT[-/TTG]TTGTTGCATTTTCTT | 121441 |
rs569483163 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96949960 | ATAATGCACTGCCTA[-/T]AAAAATACATTGGTA | 121441 |
rs569552545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96941437 | CTTACCCTGGCCTGC[A/G]AATTTCTATTTAAAT | 121441 |
rs569672398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932947 | CAGAGGTTTGCTGAG[C/T]GTCCACTGAACTTAG | 121441 |
rs569698508 | in-del | -/TT | 0.0123036 | 0.0774623 | intron-variant | NEDD1 | GRCh38.p7 | 12:96915416 | CCTTTAAAGAATCTC[-/TT]TTGAGCAGAGGATAT | 121441 |
rs569806842 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96933767 | AGAATTAAGTAGAAT[A/T]TAAATTCATAGGGAA | 121441 |
rs569807169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917922 | TGTCTTTTTTCTTAC[A/G]TGTGTAGCATTAATG | 121441 |
rs569883124 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96925687 | AATTCTATGTGATAG[G/T]TTGCTGTATTGTTAA | 121441 |
rs569888180 | snp | A/G | 5.73082e-05 | 0.00535265 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909704 | CCTTTTTTTGAGTAT[A/G]TCTATTCTTAAATGT | 121441 |
rs570112493 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96940542 | TATCAGAGATGGTAA[A/G]TCTGTTCAGAGGATC | 121441 |
rs570171947 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96907274 | CGCGGAGCCGGCCGC[C/G]GCCCCCTGTTGTGTT | 121441 |
rs570362906 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96947040 | GTAAGGGTATTATTC[A/T]ATAATTATCTATTAG | 121441 |
rs570419812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913488 | AAGCGATTCTCCTGC[C/T]TCAGCCTCTCAAGTG | 121441 |
rs570448605 | in-del | -/TGAG | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96950833 | TGTGTGGTGGGTGAC[-/TGAG]TGTTTCTTTTGTTAT | 121441 |
rs570488049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944987 | GTTAAATTCAGGTAC[A/G]TTGATTTGATCTTTT | 121441 |
rs570507754 | snp | C/G | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953322 | TACTAATAATTACTT[C/G]CAAAAATAAAAACAG | 121441 |
rs570560083 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952827 | CAACATGACAACTTA[C/T]AATGAGTGGAGATTT | 121441 |
rs570597705 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945569 | CAGTGAATTTTTCTA[A/C]ATGTCACAGGAACAC | 121441 |
rs570793836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951172 | TATATCTACTCTGGT[C/T]AAGTTATTTCTTTTG | 121441 |
rs570879965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935365 | TTCTTCTTATGCAGA[A/G]AGAAATAGATGGGTT | 121441 |
rs570972496 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96920968 | TAATACAGATATATA[A/C]ATGGTATTATGAGTA | 121441 |
rs571000195 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937072 | GGGAAACTCAGGTCT[G/T]CCAGCAAGCTTAAGA | 121441 |
rs571011242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912950 | TAAGCTCAAAATAAT[A/G]TAGTAACACTTAAAA | 121441 |
rs571028647 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96927596 | CCTTAGATTAAAAAA[C/T]GATCTTTAAATGTAG | 121441 |
rs571038814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928546 | CATAGCTTTTGAAAC[C/T]CTTTTAAGTCACTAG | 121441 |
rs571079846 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96921579 | CCTTACATGGAGAAG[A/T]TGTATAATAAATATT | 121441 |
rs571113059 | snp | G/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953542 | TTAATATTTTCCTGT[G/T]GCTTTTTTAAAAAAA | 121441 |
rs571140820 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96916704 | TATTGTGAGTAATGC[C/T]GCAATAAACATACGT | 121441 |
rs571162687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96926732 | GCACAGTGGTTCACA[C/T]CTGGAATCCCAGCAC | 121441 |
rs571170073 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96924265 | AGCTTTATGGTAGAT[C/T]GTGATATTTTTAAGT | 121441 |
rs571201516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96925971 | AACTTGAACAAGTTA[C/T]TTAACTCTCAAGCCT | 121441 |
rs571290142 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917335 | CAAGCCCTGATGGGA[C/G]ACCAGGACTGCCAGT | 121441 |
rs571383582 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96909980 | AATGAAACTTTTGCA[C/T]GTGCCTCATACTGAG | 121441 |
rs571390766 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96908183 | GTGTTACATCTCTGC[A/T]GGTGACTTTAATGGC | 121441 |
rs571405051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96919674 | TTCATTTAGCATATT[C/T]TCTGCCATTTTCATG | 121441 |
rs571441714 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932189 | CTTATACTGCCGGGA[-/T]TTTTTTCCCCCCCAT | 121441 |
rs571484998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96950295 | TCTTGATGATATAGA[A/G]CAAGAAGAACTCTGT | 121441 |
rs571487632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96911537 | ATAGTATAGATTCCA[A/G]GAATGGGGTTAATGT | 121441 |
rs571574667 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96937873 | ATTTAGACTTTATTG[A/T]TGTGTTATATGATAA | 121441 |
rs571638828 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943118 | ACTAGGTCCAAGCCA[C/T]GTTCAAAGGGAGGAG | 121441 |
rs571650817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934672 | CCTCCCAAGTAGCTG[C/T]AATTACAGGCGCCTG | 121441 |
rs571722267 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96913924 | AAACAGCAGGACAAC[G/T]GAATAAAAGCTCAAC | 121441 |
rs571888221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96914620 | CCAAGTCCTCTTACT[C/T]GTGTATTATTTGAGG | 121441 |
rs571915554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930307 | TTCTCTAGGAGAACT[C/T]ACAGGATTCTGTATA | 121441 |
rs572013717 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930950 | TTAAGCAAAAGACAA[A/C]TATGTTGAGATTTTT | 121441 |
rs572055886 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908724 | GTTTTGGAAAAACTG[C/G]TGTGACTGGATTCTG | 121441 |
rs572467236 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96929916 | GGCCACCATGCTTTT[C/T]TGTGAATACCTTTTG | 121441 |
rs572469148 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951770 | ATTTTCCAAATATAC[G/T]AATTTCACCAACGAT | 121441 |
rs572557577 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952416 | TTGACAAATTGCCTT[C/T]CAAATTTTTGGGGCT | 121441 |
rs572584452 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96950820 | CTAGTTCATAAGTTG[C/T]GTGGTGGGTGACTGA | 121441 |
rs572585808 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906994 | TGGCACACAGTAAAC[A/G]GCAAGTGAATGACAA | 121441 |
rs572621895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943941 | ATATGTTGAAGGTTA[C/T]AGCAGATGGAAAGTT | 121441 |
rs572665652 | in-del | -/T | 0.0912534 | 0.193131 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934501 | TTTTCTTTTCTTTTC[-/T]TTTTTTTTTTTTAAG | 121441 |
rs572807224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96938167 | TATTTCCAAGTAGAA[A/G]CAAAACTTTAATTTG | 121441 |
rs572908510 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936503 | ATGTGTGCTCTTTGA[A/C]CAGTTTGAAGTGTTA | 121441 |
rs573070850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96918527 | TTGATGATTTTTTCC[A/G]TTTTCAGCTTTCTCA | 121441 |
rs573098648 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEDD1 | GRCh38.p7 | 12:96926709 | CAGTTTAAAAATATC[A/G]TGGCCAGGCACAGTG | 121441 |
rs573098964 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEDD1 | GRCh38.p7 | 12:96924207 | TAGTCGTTCTATTTT[A/G]TTCCGTTGGTCTAGT | 121441 |
rs573109367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96919056 | AGGGCTTAGTTTGTT[C/T]GTATTATTGAGATAT | 121441 |
rs573113001 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910365 | TTGCCCAATATCTCC[A/G]TCTTACTAATGTACT | 121441 |
rs573123588 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928744 | CAGGCTGGAGTGCAG[G/T]GGCACTGTCTGGGCT | 121441 |
rs573252176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934903 | GTGTGGTTGGCCATA[A/G]TTTATATGGCTTATA | 121441 |
rs573288242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96926365 | TATATTTGTTTTGTG[C/T]ACCATTTTATTTCAT | 121441 |
rs573336856 | snp | C/T | | | utr-variant-5-prime, intron-variant | NEDD1 | GRCh38.p7 | 12:96907508 | GGGTCGCGCACCTCC[C/T]GGAGCCTTGTGGGGT | 121441 |
rs573356772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96927053 | TGTTCATAAAAATTT[C/T]AAATCTGTCAAAAAG | 121441 |
rs573462076 | in-del | -/TT | 0.000292526 | 0.0120904 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917599 | TTAAATTAAGGTAAC[-/TT]TTTTTTTTTTTTTTA | 121441 |
rs573691036 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NEDD1 | GRCh38.p7 | 12:96916718 | CCGCAATAAACATAC[A/G]TGTGCATGTGTCTTT | 121441 |
rs573736622 | snp | A/G | 1.65427e-05 | 0.00287595 | missense, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96909844 | TTGGTGGATAAATTC[A/G]ACCCACACACATCAC | 121441 |
rs573777087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945908 | TTTTTTTTTAGATGT[A/G]AAACCAGAACTATAG | 121441 |
rs573829037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917485 | GAGAGAGTGGCTCTT[C/T]AGTACAAGATTAGCA | 121441 |
rs573854153 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932705 | ATGTGGTTACTTAAG[G/T]GTCTTTTAAAAAATA | 121441 |
rs573972491 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908655 | GGCATCGTAGTCCAA[C/G]TATTGGTATAGGGAC | 121441 |
rs574000185 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96948821 | TCACTGTCTTTTTTA[C/T]CTTGGTGGGTCCCAA | 121441 |
rs574004180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942052 | TGGACTGGCAAATGA[A/G]TATTACAGGATTAAA | 121441 |
rs574136961 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940251 | TCCATGAAAATCCTG[A/G]TTAACTTTAGCTCTT | 121441 |
rs574176350 | in-del | -/C | 0.00438332 | 0.0466095 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943207 | CTTCCAAGATACATA[-/C]CCACAGATATATACC | 121441 |
rs574267550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922330 | CATAAAGTCTAAGCC[C/T]ATAAACTTTGGAACT | 121441 |
rs574271859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932186 | GCTGCTTATACTGCC[A/G]GGATTTTTTCCCCCC | 121441 |
rs574287275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96932968 | CTGAACTTAGGTTTA[C/T]CTGAAGGGAACATTT | 121441 |
rs574301689 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96922843 | CATATGTGGGCCAGA[C/T]GCGGTGGCTACCTGT | 121441 |
rs574312162 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937480 | TAATTAGCACATTCT[A/T]CAAGAACATAGAACT | 121441 |
rs574351953 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96916975 | GAGAGCTTACTGATA[G/T]ATTGGAGGGGAGGGA | 121441 |
rs574418275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923597 | CATGTTGAATGATGT[C/T]AAGTATATTTTTATA | 121441 |
rs574520963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930858 | CGTACACATGCACTC[A/G]CAGTATTGACGGTCA | 121441 |
rs574557605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913820 | TAGCTTTTTTTTTTA[A/G]TTTCAAAGTTTTTCT | 121441 |
rs574648254 | in-del | -/TTTCT | 0.0023933 | 0.0345097 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934483 | TGAAATTTGTTACCC[-/TTTCT]TTTCTTTTCTTTTCT | 121441 |
rs574725580 | in-del | -/TA | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96918981 | CACTTGAAAAAGTTG[-/TA]ATATAAGTGGAATAT | 121441 |
rs574743817 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96930458 | TCCTAGAGTAGATGT[A/G]CTTAACCCCTTCCAG | 121441 |
rs574819568 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96929290 | AAAAAATTTCTAATT[C/G]TTTCCCAAGTTCTGA | 121441 |
rs574954214 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96913111 | GTTGCTGCTATTTTA[A/G]GACGATATCCCACAT | 121441 |
rs574973337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96949012 | GTTTTCTGCAGGCCT[C/T]CTCTCTTCAAGACCT | 121441 |
rs574993057 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906365 | ATGCACTTATTAGAA[G/T]TTTCCAATTATCTGC | 121441 |
rs575008733 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96949778 | GGTAGCATTGCAGAT[G/T]TATGTGCAAAAAATG | 121441 |
rs575225690 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952271 | CTACCCAATAGGAAA[A/G]TCAACAGGATCTTTA | 121441 |
rs575359839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934006 | TGTTTAGAGAAAGGC[C/T]AGCATTGCCCTCAGG | 121441 |
rs575396933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934777 | GCCTGACCTCAGATG[A/G]TCCACCTGCCTCGGC | 121441 |
rs575398542 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96925378 | TGTGATCATTGCATT[G/T]AATTACATTGTCTCG | 121441 |
rs575435181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96926315 | ATTTGACTAGAGTCT[A/G]TTGGTTTTTTTCCCC | 121441 |
rs575448269 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935877 | AGTTGTATTCAAGAT[C/G]CTTACCACTGTCTGT | 121441 |
rs575532181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936412 | ATGGAATGTTTAGCA[A/G]TTCTCTATATGCCAT | 121441 |
rs575533593 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96911509 | TTCCCAGCCTTAGCA[A/C]CTTGGGGTCCACATA | 121441 |
rs575543377 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96927980 | AGTATTGGTATACAC[C/T]TGACTAGCCTATATA | 121441 |
rs575556658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96941233 | AGAGAAGCCCACAAA[A/G]ATTTGTGTATTTATT | 121441 |
rs575637297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96941887 | TACATGCTGTGCAAT[C/T]ACTGGGAACATATAC | 121441 |
rs575647098 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96927233 | AAAAATGATCAAATT[A/G]GTGTCTTAGTGAAAG | 121441 |
rs575650734 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951823 | AGTAAGTTGTTAAGT[A/G]CAAGAAATATCATTC | 121441 |
rs575887689 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96918467 | AACTTTCTTTAATCC[A/G]TCTCCCATGTAAGCT | 121441 |
rs575955663 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96926781 | GCAGATCACTTGAGC[C/T]CAGGAGACCAGCCTG | 121441 |
rs576107469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96923544 | CACTTTGATGGTTAT[A/G]TAGTGCTGTCTCATG | 121441 |
rs576125497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96915398 | GAAGGGGATCATATG[C/T]ACCCTTTAAAGAATC | 121441 |
rs576152192 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953246 | AAACCTTTAGCTCAC[C/T]AACTTTATGGGTTTC | 121441 |
rs576165813 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NEDD1 | GRCh38.p7 | 12:96908810 | TAGTAGTTATTTGTT[G/T]TGAAACTGCTGTGTG | 121441 |
rs576175542 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909197 | AAAAAAAAAAAAATT[C/G]AGATATTAGGAAGTG | 121441 |
rs576243255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96924197 | ATGTTAGTTGTAGTC[A/G]TTCTATTTTGTTCCG | 121441 |
rs576418932 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906307 | GCCACTCCCCCATGA[A/G]CCTCAGTAACTTGGC | 121441 |
rs576518243 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96907101 | TGGGATAACTTCCCC[C/G]GCGGCTGCCCAGCGC | 121441 |
rs576542180 | snp | C/T | 0.000512079 | 0.015993 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96945836 | ATGATACAGGAAACG[C/T]TGGATGACTTTAGGT | 121441 |
rs576555686 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96907645 | CCTCACTTGAGCTGT[G/T]GTCCTGCAAGTAAAG | 121441 |
rs576557064 | snp | G/T | 0.0123427 | 0.0775824 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937430 | TTGGAGGGTTGGTTT[G/T]TTTTTTTTTTGTTTT | 121441 |
rs576592584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96928814 | GCCTCAGCCTCCCGA[A/G]TAGCTGCGACTACAG | 121441 |
rs576662551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96939290 | TCAAATGATACCAAA[C/T]TTCTGTTTCCTAAAG | 121441 |
rs576690205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940167 | AAATAAGCTGTTTTC[C/T]TTTGAGGAACCTTTT | 121441 |
rs576724664 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944032 | ATCCCTGAATCCTTT[G/T]AAAGTGTATTTCATT | 121441 |
rs576762551 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96915615 | GAATCCAAGGATGCA[C/T]TGTGGAAGTTCCAAC | 121441 |
rs576824886 | snp | A/G | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952215 | CTGTTTCATCTTAAA[A/G]ATATGTATATTTTTA | 121441 |
rs576834464 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96931015 | CAGGATGGATAGTAA[C/G]CCACTGAGAATGGAA | 121441 |
rs576870312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944553 | ACCTACATACTGGGA[C/T]AAAAGAGAGAAGTAG | 121441 |
rs576893208 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96918749 | GCTGAATGACTTATT[C/T]TCCACAGTTGAAATT | 121441 |
rs576965594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96921285 | CTCCCGGGTTCAAGC[A/G]ATTCTCTTGTCTCAG | 121441 |
rs577004563 | snp | A/G | 0 | 0 | intron-variant | NEDD1 | GRCh38.p7 | 12:96910980 | ACTATTCTTGCATGT[A/G]TATAACAAGAAGGAC | 121441 |
rs577038360 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96948044 | AGACTAGGTGTTCAT[C/G]TACACCTATCATTGG | 121441 |
rs577074596 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905568 | TTAAACTATTATACA[A/G]AACTGAGGAAACAGT | 121441 |
rs577489328 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951006 | TGATCTTTCTAACCT[A/C]GTGAATTTTCTGTAT | 121441 |
rs577582305 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | NEDD1 | GRCh38.p7 | 12:96918179 | TTGTGTTTTTTTTTT[G/T]TGTGTGTGTGTTTGT | 121441 |
rs577599834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909107 | CTTGAACCTGGAAGG[C/T]GGAGGTTGTGGTGAG | 121441 |
rs577724746 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NEDD1 | GRCh38.p7 | 12:96948941 | TCTAACCCAGGGGGA[A/G]CATTGCTTAGAAGTC | 121441 |
rs577782448 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96933056 | AGAACTTGAAGTAAG[A/G]TACAGAATTTAGGTT | 121441 |
rs577782785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96941619 | TTAGTGCTGAATTGC[A/G]AGTTTTGGCCAGTGA | 121441 |
rs577797104 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96941039 | AAGTACATTGTTTAG[A/C/G]TGTGTCTTTTTGGTA | 121441 |
rs577821915 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEDD1 | GRCh38.p7 | 12:96933855 | CAAGTTTGACAGTAA[C/T]ATTTTAGTAAAAAAG | 121441 |
rs577865120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96949635 | TTGAAGGGGACTTAT[C/T]TGTCAGATGAATACA | 121441 |
rs577866399 | snp | C/T | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905321 | CTATGGGTATGCTTT[C/T]TTCCTCCTTTAGCTT | 121441 |
rs577940930 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96939123 | ATTTTAAGCTTTGTA[C/T]AAAATTAAAGTTCAG | 121441 |
rs577996648 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942797 | ACCTTTGCCTTCAAG[A/T]CTATCTTCCTGCTTC | 121441 |
rs578024413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943362 | TTACATTTGTAGATC[A/G]GGAAATAGTCACAGA | 121441 |
rs578030359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEDD1 | GRCh38.p7 | 12:96947453 | CAGAGAGAAGGCACC[A/G]TGGTAAGAGACCAGG | 121441 |
rs578059708 | in-del | -/TATACACTTGAGT | 0.00597247 | 0.0543191 | intron-variant | NEDD1 | GRCh38.p7 | 12:96950372 | ATGATTTTGTAAAAG[-/TATACACTTGAGT]TACAGTTGGTTATAT | 121441 |
rs578113210 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96909033 | AATACAAAATTAGCC[A/G]GGTGTGGTGGTGCAT | 121441 |
rs745317408 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96933437 | TAATGCACTAAGTAG[G/T]TCTGTGTCTTTTATA | 121441 |
rs745401167 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96932061 | AAGTTTTTGAAACCT[C/T]CCCCCCACCTTTAGT | 121441 |
rs745403293 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96947009 | TCTTCCATTAAGTGA[C/T]CATCACTTCTTCACA | 121441 |
rs745410616 | snp | C/T | 0.000120024 | 0.00774582 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936589 | TAACATTTCTACACA[C/T]ACTTTGTTCTCCTTT | 121441 |
rs745447349 | snp | A/G | 1.66443e-05 | 0.00288477 | missense | NEDD1 | GRCh38.p7 | 12:96945704 | TTAGATCCAAAGATA[A/G]CATCTTCTGTCACTG | 121441 |
rs745467707 | snp | A/T | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952844 | ATGAGTGGAGATTTC[A/T]TATTAGGTACTAAAT | 121441 |
rs745481361 | in-del | -/TTTG | 1.77836e-05 | 0.00298186 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937444 | GTTTTTTTTTTGTTT[-/TTTG]TTTTGTTTTTGGCTT | 121441 |
rs745514946 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96919042 | TAATTATTAGATACA[A/G]GGCTTAGTTTGTTTG | 121441 |
rs745557686 | snp | C/T | 1.65012e-05 | 0.00287234 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96945811 | CATTCAAATTCGTTT[C/T]ATTCAGAACATGATA | 121441 |
rs745662075 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96941667 | TTTTGCATTGAAGAA[C/T]GTACAAAGGGGCTTT | 121441 |
rs745695638 | snp | A/G | | | downstream-variant-500B | NEDD1 | GRCh38.p7 | 12:96954161 | TTAGAAGGAAATTAT[A/G]CCAAATAGAAATCTG | 121441 |
rs745785263 | snp | A/C | 3.306e-05 | 0.00406558 | missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96920054 | GCTTCTGGATCTCTT[A/C]GTGGTGAAATTATTT | 121441 |
rs745815626 | snp | C/G | 0.000186585 | 0.00965699 | intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96924836 | TGCGTTGACTAGGCT[C/G]TCCAATCCAGTGTTG | 121441 |
rs745854415 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96943370 | GTAGATCGGGAAATA[A/G]TCACAGAAAGTTTAA | 121441 |
rs745942162 | in-del | -/AACAC | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96909915 | CCTTTAAAAAAAAAA[-/AACAC]ACACACACACACACA | 121441 |
rs745954859 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96927732 | CTTGAGTATGGAGAT[A/C]TGATAAATGTAAATA | 121441 |
rs745997332 | snp | A/G | 1.67273e-05 | 0.00289195 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936817 | TTCTTACTAAGGTGA[A/G]ACATTTTCTTTTCAG | 121441 |
rs746002337 | in-del | -/T | 0.0392 | 0.1344 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917598 | TTAAATTAAGGTAAC[-/T]TTTTTTTTTTTTTTT | 121441 |
rs746064339 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96948249 | TACACTTGTCCCTAC[-/T]TTTTTTTACATGAGC | 121441 |
rs746100768 | snp | A/G | 1.65425e-05 | 0.00287593 | missense | NEDD1 | GRCh38.p7 | 12:96937243 | CCCACAACAGTGAAC[A/G]AACGAAGTGTTAATG | 121441 |
rs746103595 | snp | C/T | 1.65817e-05 | 0.00287933 | synonymous-codon, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96917642 | CAGACATGTGTCAAT[C/T]TAAATTCTACATCTA | 121441 |
rs746126812 | snp | A/G | 1.67635e-05 | 0.00289507 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96951966 | TGAAATGCATTCTTT[A/G]CTGGAAAGATACTCA | 121441 |
rs746148680 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96949934 | CATGGTAGGAAATCA[C/T]TAAAAATAAAATAAT | 121441 |
rs746154989 | in-del | -/TAAACAA | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96936470 | TCTGAAATTATGCTT[-/TAAACAA]ATATTTGGGATATGT | 121441 |
rs746171470 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96937900 | ATAAGCTTTCTCTTA[G/T]TGTAGAAAATATTTC | 121441 |
rs746195763 | snp | A/T | 1.66743e-05 | 0.00288736 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917749 | TAAGGTAAGCAATTT[A/T]AAAAAAATCTTCATG | 121441 |
rs746263220 | snp | A/G | | | missense | NEDD1 | GRCh38.p7 | 12:96936790 | AGTGTATAGCATTTC[A/G]GTACTCCACTGTTCT | 121441 |
rs746285060 | snp | C/G | 1.84113e-05 | 0.00303402 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952096 | TAATTTGGGAAGTTT[C/G]TGGCAACACAGAACT | 121441 |
rs746309604 | snp | A/G | 1.65296e-05 | 0.00287481 | missense | NEDD1 | GRCh38.p7 | 12:96942619 | AGTCCATAGGCAAAG[A/G]AGATGGTAAGAACTA | 121441 |
rs746399294 | snp | A/G | 1.65548e-05 | 0.002877 | missense | NEDD1 | GRCh38.p7 | 12:96943566 | CTTTTCCAGGCTTTG[A/G]CTTTCTACCGCAGTT | 121441 |
rs746405122 | snp | A/T | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905887 | ACTTCATGTGTTTTT[A/T]GAAAGATGAAATTAT | 121441 |
rs746410089 | snp | C/T | 1.64942e-05 | 0.00287173 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96935179 | CTTGGATAAAAGAAT[C/T]ATCCTCTATGACACT | 121441 |
rs746424262 | in-del | -/TAG | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96916901 | GGTTTGGGTTAGTGT[-/TAG]TAGTAGCTATAGATA | 121441 |
rs746428323 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96937156 | AATGTATAGTATGAA[A/C]CATTAGTAACCTGAG | 121441 |
rs746437326 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96922531 | TGCTTATTGTATCTT[A/G]CTAGAGAGTTTTCTT | 121441 |
rs746454363 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96919312 | GTCACTTAGCAGTTA[C/T]GTGAGCTTGCGCAGG | 121441 |
rs746467853 | in-del | -/ATA | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96918785 | GACACTTGCCTCTTT[-/ATA]AAGTCATAGAAATTA | 121441 |
rs746555723 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96922337 | TCTAAGCCTATAAAC[-/T]TTGGAACTATTGTGA | 121441 |
rs746596709 | snp | A/C | 1.6679e-05 | 0.00288777 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951392 | ACCTAGAATTGGTTA[A/C]ACTATTGTAATTCTA | 121441 |
rs746598713 | snp | G/T | 5.07924e-05 | 0.00503921 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937434 | AGGGTTGGTTTGTTT[G/T]TTTTTTGTTTTTTTG | 121441 |
rs746630303 | snp | C/T | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906439 | ACACACCCCATGTAG[C/T]TGTGATGAAAGAATA | 121441 |
rs746684519 | snp | A/G | 1.70058e-05 | 0.00291592 | missense | NEDD1 | GRCh38.p7 | 12:96940409 | TCTAATTCCTATAAG[A/G]TTTGCCTCGAAGCAT | 121441 |
rs746718346 | snp | C/T | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905429 | TTTACCATTTTATCA[C/T]TATGAAATATTTCTC | 121441 |
rs746782896 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96939918 | AAGAAAAGACAGAAA[A/T]CCCCTTCACTGCAAG | 121441 |
rs746909964 | snp | C/T | 4.94841e-05 | 0.00497389 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96934996 | TCGGCACTTGAAGTA[C/T]TCCTTGTTTAAGAAA | 121441 |
rs746956699 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96946883 | TCTTTTTATTCACTT[C/G]CTCTTGGCTTGGCTG | 121441 |
rs747038233 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96913330 | AATGAGCTTAGGTCC[C/T]AGGGCGTTTAAATGA | 121441 |
rs747059783 | in-del | -/T | 0.010558 | 0.0718854 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937431 | TGGAGGGTTGGTTTG[-/T]TTTTTTTTTGTTTTT | 121441 |
rs747156788 | snp | C/T | 1.64863e-05 | 0.00287104 | missense | NEDD1 | GRCh38.p7 | 12:96937316 | GAGAAGCACCTGCCA[C/T]GTCCATTGCCACAGT | 121441 |
rs747225218 | in-del | -/AAAAAAA | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96932443 | AAAATCCTGTCTCTT[-/AAAAAAA]AAAAAAAAAAAAAAA | 121441 |
rs747244641 | snp | A/G | 0.000233333 | 0.0107987 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917764 | AAAAAAAATCTTCAT[A/G]AAAAAATGGATATCT | 121441 |
rs747309584 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96908614 | AATTACGTGTTTCAG[C/T]TGTATGCTCTGAATA | 121441 |
rs747455835 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96908086 | TTAGAGCTCGCTTTT[C/T]CAGCAATTCATTAGT | 121441 |
rs747472341 | in-del | -/A | 7.20137e-05 | 0.00600014 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917614 | TTTTTTTTTTTTTTT[-/A]AAATAGCAAAAGCAG | 121441 |
rs747535750 | snp | A/T | 3.30901e-05 | 0.00406743 | synonymous-codon, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96909855 | ATTCAACCCACACAC[A/T]TCACCACATGGAATC | 121441 |
rs747535905 | snp | A/G | 1.65162e-05 | 0.00287365 | missense | NEDD1 | GRCh38.p7 | 12:96936684 | GGAGCCACTTTGGCT[A/G]TTGGATCTTCCCGGG | 121441 |
rs747545225 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96910621 | TTGTGGACCTTTCCT[A/G]TATGTTGTACCACGT | 121441 |
rs747566646 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96945627 | ACATGCCAAATCTTA[C/T]TTAGAAATGTTTGAT | 121441 |
rs747664064 | snp | G/T | 1.95884e-05 | 0.00312951 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951914 | AATAAATGTGAAATA[G/T]CAATAATTTAAAAAG | 121441 |
rs747701880 | snp | C/T | 1.67027e-05 | 0.00288982 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96940422 | AGGTTTGCCTCGAAG[C/T]ATAAACACAGACACT | 121441 |
rs747706393 | in-del | -/TTTTA | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96937964 | TGAAAACCTTTTCAT[-/TTTTA]TTTTAAGAAGTTATG | 121441 |
rs747715519 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96920878 | ACTTGAATAGTATTT[A/C]GTGCTTAAAAAATTT | 121441 |
rs747798095 | snp | C/T | 2.48117e-05 | 0.00352211 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934927 | GCTTATATCAAATGT[C/T]CTTATGAATGCTTAT | 121441 |
rs747798181 | snp | C/T | 1.65858e-05 | 0.00287969 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96940521 | TTTAGGTGACATGTT[C/T]TCACCTATCAGAGAT | 121441 |
rs747808314 | snp | A/G | 1.648e-05 | 0.0028705 | missense | NEDD1 | GRCh38.p7 | 12:96935021 | AAGAAATCACTACTG[A/G]GCAGTGTTTCGGATA | 121441 |
rs747877565 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96931497 | AAGTAGAATAATGAG[C/T]AGTTTGCAAAAGAAG | 121441 |
rs747962032 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930352 | GCTATGATTTATTTT[A/G]TAGTGAAAGAATACA | 121441 |
rs748009581 | snp | A/G | 1.90445e-05 | 0.00308576 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909708 | TTTTTGAGTATGTCT[A/G]TTCTTAAATGTTTTT | 121441 |
rs748019172 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96950310 | GCAAGAAGAACTCTG[G/T]TATACTGGTGACATC | 121441 |
rs748028572 | snp | A/G | 1.68485e-05 | 0.00290241 | missense | NEDD1 | GRCh38.p7 | 12:96944778 | GTGAACCCCCAATCA[A/G]TGGATCCTCAACTCC | 121441 |
rs748114416 | snp | C/T | 0.000108311 | 0.00735825 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945669 | CAAGTTGACTATTAA[C/T]ATTTTCTTCATTCTT | 121441 |
rs748119776 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96922715 | GAATTTTTATGTATA[C/T]GTAAATACATTGGTG | 121441 |
rs748129847 | in-del | -/CTG | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96928761 | CACTGTCTGGGCTCA[-/CTG]CTGCAAGCTCCGCCT | 121441 |
rs748148147 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96915569 | CTTTTAACTTTTCTT[A/G]AAGTCATGAAATGTC | 121441 |
rs748148778 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96951236 | GAAGATATTTTAAAC[A/G]AGTTCTTACATTTAA | 121441 |
rs748185733 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96939982 | CTGTATGTTAGGCAT[C/T]GCTCTATATGCCTTA | 121441 |
rs748197987 | snp | C/T | 4.96833e-05 | 0.00498389 | synonymous-codon, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96920017 | AACTTGTGTAACATA[C/T]AATTGGAATGATTGC | 121441 |
rs748233020 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96929224 | TATTGTCTGTTGTGT[A/T]TATTCATTTTTGAAT | 121441 |
rs748239125 | snp | C/T | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952390 | TCATCTTTTTTAACA[C/T]ATATTTTTGATTGAC | 121441 |
rs748273638 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96938570 | CAAATCAAAGGCTTG[A/G]ATCTTTCAGGGTCAT | 121441 |
rs748322754 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96932686 | GAGACATTTAAAGAA[C/T]TCAATGTGGTTACTT | 121441 |
rs748331465 | snp | A/G | 1.65061e-05 | 0.00287277 | missense | NEDD1 | GRCh38.p7 | 12:96943608 | TTCCTCCAAGAAAAA[A/G]TCCAGTAACTTCAAG | 121441 |
rs748449198 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96947242 | AGTGCATAAATATTT[A/G]TGGCATAATAGTAGA | 121441 |
rs748465459 | in-del | -/G | 7.55677e-05 | 0.00614639 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937441 | GTTTGTTTTTTTTTT[-/G]TTTTTTTGTTTTTGG | 121441 |
rs748470623 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96923959 | CTTGAAGAATCTTGC[C/T]TGCCCCAAGATTTTG | 121441 |
rs748497881 | snp | A/G/T | 4.9558e-05 | 0.00497764 | missense | NEDD1 | GRCh38.p7 | 12:96936697 | CTATTGGATCTTCCC[A/G/T]GGGGAAAATATATCA | 121441 |
rs748531866 | in-del | -/TATG | 1.65619e-05 | 0.00287762 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917744 | CTCTTAAGGTAAGCA[-/TATG]ATTTAAAAAAAATCT | 121441 |
rs748689394 | snp | A/T | 1.64855e-05 | 0.00287097 | missense, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96912775 | AATAGTTGTCTCAAG[A/T]TGCAAATGTAAACCT | 121441 |
rs748717903 | snp | A/G | 1.66421e-05 | 0.00288458 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951411 | ATTGTAATTCTAAAA[A/G]GTATTTTACATTCTT | 121441 |
rs748800957 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96940364 | GCTTATGATAAAATT[G/T]ATTTAGATGTAATAA | 121441 |
rs748866951 | snp | C/T | 8.23879e-05 | 0.00641772 | missense | NEDD1 | GRCh38.p7 | 12:96935031 | TACTGGGCAGTGTTT[C/T]GGATAATGGAATAGT | 121441 |
rs748878028 | snp | A/C | 1.64882e-05 | 0.00287121 | missense | NEDD1 | GRCh38.p7 | 12:96935171 | ACCATAGGCTTGGAT[A/C]AAAGAATCATCCTCT | 121441 |
rs748901368 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96943088 | TTTTCATATTACTTT[C/T]GTTAGAAGCAAGTTA | 121441 |
rs748943154 | snp | A/G | 3.63683e-05 | 0.00426413 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909727 | TTAAATGTTTTTAAA[A/G]TACATTGTTTTAAAC | 121441 |
rs749012153 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96913426 | TTGCCCAGGCTGGAG[C/T]GCAATGGTGCAATCT | 121441 |
rs749055968 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96915765 | GAACTTGACAACATC[C/T]GTATTTTAGCCATTC | 121441 |
rs749160041 | snp | G/T | 5.10738e-05 | 0.00505315 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945687 | TTTCTTCATTCTTTA[G/T]TTTAGATCCAAAGAT | 121441 |
rs749180864 | snp | C/G/T | 1.65042e-05 | 0.0028726 | missense | NEDD1 | GRCh38.p7 | 12:96945795 | ATGCACCATTGACTT[C/G/T]CATTCAAATTCGTTT | 121441 |
rs749230650 | snp | A/C | 1.64887e-05 | 0.00287125 | missense | NEDD1 | GRCh38.p7 | 12:96937336 | ATTGCCACAGTTCTA[A/C]CACAACCTATGACAT | 121441 |
rs749249130 | snp | A/G | 1.6945e-05 | 0.00291071 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937421 | TATATATTGTTGGAG[A/G]GTTGGTTTGTTTTTT | 121441 |
rs749283748 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96940041 | TGATCATGAGTCAGT[C/G]AATAGCAAAAGTAAG | 121441 |
rs749318772 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96926211 | TAGATTTAATGTGTT[C/G]CCTCCAAACCCAGTT | 121441 |
rs749407151 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96924637 | AGAAACACAGTTCAT[A/G]TTTGTCTTTTGTCAT | 121441 |
rs749407235 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96941508 | GGATGAAGAGAAGTC[A/G]AACTACATCAAACTA | 121441 |
rs749421676 | snp | A/G | 1.70746e-05 | 0.00292182 | missense | NEDD1 | GRCh38.p7 | 12:96943746 | GAAAACAGGAATCTA[A/G]AGACTCCTTCAAACA | 121441 |
rs749424865 | in-del | -/C | 6.70815e-05 | 0.00579105 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909911 | TATCCTTTAAAAAAA[-/C]AAAAACACACACACA | 121441 |
rs749505850 | snp | C/T | 1.65121e-05 | 0.00287329 | missense | NEDD1 | GRCh38.p7 | 12:96936708 | TCCCGGGGGAAAATA[C/T]ATCAATATGATTTAA | 121441 |
rs749524308 | snp | C/T | 1.65482e-05 | 0.00287643 | missense | NEDD1 | GRCh38.p7 | 12:96936799 | CATTTCAGTACTCCA[C/T]TGTTCTTACTAAGGT | 121441 |
rs749564886 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96947480 | CAGGCCTGAGGGACA[C/G]TTGTGAAGGTCTTAA | 121441 |
rs749572795 | in-del | -/ATATC | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906001 | TGTATAACTAGTATT[-/ATATC]ATATAATATGTATAT | 121441 |
rs749574143 | snp | C/G | 6.59413e-05 | 0.00574163 | missense, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96912791 | TGCAAATGTAAACCT[C/G]TTCCACTTTTAGAGC | 121441 |
rs749590181 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96911482 | GGAGGTTAATTACTG[A/C]AGAACAAGGAGTTCC | 121441 |
rs749598933 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96935403 | GTATTTAGGGTACTT[A/C]TGAAACATGAACATA | 121441 |
rs749632347 | in-del | -/T | 3.45913e-05 | 0.00415866 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952056 | GGCCCACTTTTGAAA[-/T]TTCAGTGAATACCTT | 121441 |
rs749779111 | snp | C/G | | | missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96917631 | AATAGCAAAAGCAGA[C/G]ATGTGTCAATTTAAA | 121441 |
rs749797166 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96919796 | AATTACCTGTCCATA[A/G]TCTCTCTCTCTCGTA | 121441 |
rs749826269 | snp | A/C/G | 3.34187e-05 | 0.0040876 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940551 | TGGTAAGTCTGTTCA[A/C/G]AGGATCCTGTTCTCT | 121441 |
rs749835487 | snp | G/T | 3.55897e-05 | 0.00421825 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952071 | TTTCAGTGAATACCT[G/T]AATGTTCTGTAATTT | 121441 |
rs749889247 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96912253 | TGTTCTGGGAAAATA[G/T]CAGGCCTTTTTTTTT | 121441 |
rs749896608 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96948045 | GACTAGGTGTTCATC[C/T]ACACCTATCATTGGC | 121441 |
rs749915344 | snp | C/G | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906458 | GATGAAAGAATAACA[C/G]TTTTTGCAGAAGAAA | 121441 |
rs749990838 | snp | A/G | 3.31444e-05 | 0.00407076 | missense | NEDD1 | GRCh38.p7 | 12:96943695 | AGGAAAATGAAAACC[A/G]TGATCTAACAGCTGA | 121441 |
rs750031447 | in-del | -/TAAA | 3.78874e-05 | 0.00435227 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909713 | GAGTATGTCTATTCT[-/TAAA]TGTTTTTAAAATACA | 121441 |
rs750041676 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96946638 | GTATATGTACCAGAT[A/G]CTAAGGATACATCAA | 121441 |
rs750084548 | snp | A/G | 7.54575e-05 | 0.00614191 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944601 | AATATGAGTAAAAAA[A/G]TTGTATATTAAAGTC | 121441 |
rs750088687 | snp | C/T | 1.65272e-05 | 0.0028746 | missense | NEDD1 | GRCh38.p7 | 12:96936663 | GCGGTAGATTTCATG[C/T]CTGATGGAGCCACTT | 121441 |
rs750095362 | snp | A/G | 3.39041e-05 | 0.00411714 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909922 | AAAAAAAAAACACAC[A/G]CACACACACACAAAC | 121441 |
rs750107162 | snp | A/G | 1.65081e-05 | 0.00287293 | missense | NEDD1 | GRCh38.p7 | 12:96936756 | GTTAAGACCATCAGT[A/G]CTCACAAGACATCTG | 121441 |
rs750133559 | in-del | -/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96920156 | ATTCAGAGTAAAATT[-/G]GTAAGATAGATTTTG | 121441 |
rs750158867 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96949031 | TCTTCAAGACCTTGG[C/T]TCTTACAGCCTTGGC | 121441 |
rs750232919 | snp | A/T | 3.40003e-05 | 0.00412298 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945901 | TACTTGTTTTTTTTT[A/T]AGATGTAAAACCAGA | 121441 |
rs750278688 | in-del | -/ATTA | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96931180 | TGTTAAGATGTTTGT[-/ATTA]ATTTCTTACTGCTTT | 121441 |
rs750343101 | snp | A/G | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906303 | TTTTGCCACTCCCCC[A/G]TGAACCTCAGTAACT | 121441 |
rs750346598 | snp | A/G | 2.05645e-05 | 0.00320653 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912858 | CTTTTAAAAATCTTA[A/G]TTTTGCTTGACTGGC | 121441 |
rs750387453 | snp | C/G | 1.65575e-05 | 0.00287724 | missense | NEDD1 | GRCh38.p7 | 12:96940486 | GATTTCTCCAGCTTT[C/G]ATGATACTGGGAAAA | 121441 |
rs750396090 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96936243 | ATAAATGGAAAGTGG[A/T]TACTTAGGCCCTCCT | 121441 |
rs750404796 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96945264 | TAAATATCTATATTT[C/T]GCTTGAAGTTTTCTG | 121441 |
rs750416970 | snp | A/G | 1.79725e-05 | 0.00299766 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935245 | AATTTAGTAACAAAT[A/G]GCTATTATTCCATTA | 121441 |
rs750470345 | snp | G/T | 1.90601e-05 | 0.00308702 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909703 | ACCTTTTTTTGAGTA[G/T]GTCTATTCTTAAATG | 121441 |
rs750545072 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96910141 | ATTTGAAAACACTGC[C/T]ATTAAAAAAAGTATA | 121441 |
rs750577784 | snp | A/G | 1.65214e-05 | 0.0028741 | synonymous-codon, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96909786 | CCTCAGATTTGCTTC[A/G]TCAGGAGATGATATT | 121441 |
rs750589237 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96941389 | AGGAATAAATACATA[C/T]GTGGTGGTACAGAAT | 121441 |
rs750603561 | in-del | -/T | 7.70809e-05 | 0.00620762 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936846 | GCATTTTTTATTTTA[-/T]TTAAATAAATCTAAC | 121441 |
rs750626795 | snp | C/G/T | 4.94575e-05 | 0.00497259 | missense | NEDD1 | GRCh38.p7 | 12:96937313 | TCAGAGAAGCACCTG[C/G/T]CACGTCCATTGCCAC | 121441 |
rs750670058 | snp | A/G | 3.30404e-05 | 0.00406437 | missense | NEDD1 | GRCh38.p7 | 12:96945755 | TCAGAAAAAATAGCC[A/G]ACAGCATTGGAAATA | 121441 |
rs750670674 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96931124 | GGAGTCAAAGGAACA[C/T]TATATTTATGGCCAT | 121441 |
rs750708051 | in-del | -/C | 1.65051e-05 | 0.00287267 | frameshift-variant | NEDD1 | GRCh38.p7 | 12:96945785 | AACCGGCAAAATGCA[-/C]CATTGACTTCCATTC | 121441 |
rs750762454 | snp | G/T | 1.65806e-05 | 0.00287924 | splice-donor-variant | NEDD1 | GRCh38.p7 | 12:96937394 | TTCAAGAAAAAGCAG[G/T]TAAATGTTGCTTATA | 121441 |
rs750783348 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96950772 | TAGAATCAGACAGGA[A/G]CACACAGGAAGCTTC | 121441 |
rs750910723 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96923542 | GCCACTTTGATGGTT[A/G]TGTAGTGCTGTCTCA | 121441 |
rs750911180 | snp | A/G | 1.67198e-05 | 0.0028913 | missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96919991 | CTCTTTCAGGATCAT[A/G]AAGATCAAGTAACTT | 121441 |
rs750996411 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96939446 | AATATTTTAACTTTA[C/T]AGCAGGTGTTATTAG | 121441 |
rs750998383 | snp | A/G | 1.70342e-05 | 0.00291836 | intron-variant | NEDD1 | GRCh38.p7 | 12:96920135 | AACCAGGTACAGTAT[A/G]AGTTTATTCAGAGTA | 121441 |
rs751019364 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96950449 | TAATACATGATTGTT[C/T]ATAACAACGTTGGAA | 121441 |
rs751044827 | snp | A/T | 3.31439e-05 | 0.00407073 | missense | NEDD1 | GRCh38.p7 | 12:96944740 | TGAAAAGCCAGAGAA[A/T]GAAATTGAAGCCCAG | 121441 |
rs751106428 | snp | A/G | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952403 | CATATATTTTTGATT[A/G]ACAAATTGCCTTTCA | 121441 |
rs751231719 | snp | C/T | 2.46418e-05 | 0.00351003 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937168 | GAAACATTAGTAACC[C/T]GAGCTTTTAAATATT | 121441 |
rs751317188 | in-del | -/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96943208 | CTTCCAAGATACATA[-/C]CACAGATATATACCA | 121441 |
rs751317553 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96920685 | AAAAATGTTCAAAAG[A/C]ATAAATTCAGTTTTT | 121441 |
rs751321635 | snp | C/T | 1.81105e-05 | 0.00300914 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917581 | AGTCAGCTCTGGGCT[C/T]TGTTAAATTAAGGTA | 121441 |
rs751358780 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96908079 | ACAGGGCTTAGAGCT[A/C]GCTTTTCCAGCAATT | 121441 |
rs751393717 | snp | A/G | 4.96594e-05 | 0.00498269 | missense | NEDD1 | GRCh38.p7 | 12:96940499 | TTGATGATACTGGGA[A/G]AAGTAGTTTAGGTGA | 121441 |
rs751393737 | snp | A/T | 1.68741e-05 | 0.00290461 | missense | NEDD1 | GRCh38.p7 | 12:96952035 | AGAAGAAAACAAAAG[A/T]TTACGGGCCCACTTT | 121441 |
rs751479647 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96931334 | TAAATATATAAAAAT[C/T]TAAAACTTCTGACAA | 121441 |
rs751481510 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96946455 | TAACCTATAGTTAAT[A/G]TTGTAGCTCAGATTT | 121441 |
rs751481713 | snp | A/G | 3.30469e-05 | 0.00406477 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96942593 | TGCTGTAGTTAACAA[A/G]GGAAGTGATGAGTCC | 121441 |
rs751523284 | snp | A/G | 1.64776e-05 | 0.00287028 | missense | NEDD1 | GRCh38.p7 | 12:96935103 | TTGACAGTGTACACA[A/G]AGCTCCAGCGTCAGG | 121441 |
rs751541569 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96909007 | CATGGAGAAACCCCG[C/T]CTCTACTAAAAATAC | 121441 |
rs751567089 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96945373 | TTTAATAGTCTTGGT[G/T]TATCTAGTTTATGGT | 121441 |
rs751602643 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96932730 | AAAATATGTAAAAGA[C/T]GGTTGAATGGTGGGT | 121441 |
rs751615253 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96912673 | TCTTATAATAGTCTA[C/G]TGCTATAGATGTTCA | 121441 |
rs751619803 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96915328 | GAGAGTGGCTCTTTA[C/G]TACAAGATTAGCATG | 121441 |
rs751700974 | in-del | -/TAG | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96915472 | TAAGAACAGTAGATC[-/TAG]TAGTCTTCACCTTTC | 121441 |
rs751732598 | snp | C/G/T | 3.3231e-05 | 0.0040761 | missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96920004 | ATAAAGATCAAGTAA[C/G/T]TTGTGTAACATACAA | 121441 |
rs751745008 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96917536 | ACCAATATTTATCAT[A/G]TGCTTACTAAGTGTT | 121441 |
rs751751718 | in-del | -/T | 0.0763445 | 0.179844 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945892 | TCTAGACCTTACTTG[-/T]TTTTTTTTTAGATGT | 121441 |
rs751761695 | in-del | -/AATATGAAA | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96918401 | TCTTAAAAAAGTTTT[-/AATATGAAA]AATATGAAAAATATA | 121441 |
rs751807877 | snp | A/T | 2.09721e-05 | 0.00323815 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940374 | AAATTTATTTAGATG[A/T]AATAACATTGATTTT | 121441 |
rs751820965 | snp | C/T | 1.6596e-05 | 0.00288058 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945868 | GTAATTGAGAAACTA[C/T]TCCTTCTATCTAGAC | 121441 |
rs751895984 | snp | C/T | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952299 | TTATTTTTTGAAAGC[C/T]TTAGCCATCCACTAA | 121441 |
rs751983966 | snp | A/C | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953439 | TATGAAAGCATTATG[A/C]CTTGTAACAAGTTTC | 121441 |
rs752015956 | in-del | -/TG | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96926991 | AAAAAAAAAAAATTG[-/TG]TGTGTGTGTGTGTGT | 121441 |
rs752017286 | snp | A/G | 1.74333e-05 | 0.00295235 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944613 | AAAATTGTATATTAA[A/G]GTCATTATTTATTTT | 121441 |
rs752030641 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96911176 | TATGAAGTTGCTGTT[C/T]TCTATTTTTAGATTT | 121441 |
rs752080798 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96922127 | TTAGTTGAATGTCAG[A/G]ATCATAGAATCCTTG | 121441 |
rs752135030 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96939366 | AAAAGGAGAGGAAAT[G/T]TCTTCTTTGTAACAA | 121441 |
rs752168303 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96937719 | TCATTGTGTCTTCAG[A/C]TTAACCAGTAGAAAA | 121441 |
rs752170973 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96925831 | GAACTTGAGATCTTC[A/G]TGGGCCTGCTGCCTC | 121441 |
rs752201768 | snp | A/T | 1.64898e-05 | 0.00287135 | missense | NEDD1 | GRCh38.p7 | 12:96937294 | GTTCAGAATTCCGGA[A/T]TTGTCAGAGAAGCAC | 121441 |
rs752283857 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930123 | TCCGTGGGATTTTAG[-/T]TTTTTGGTCATCTAG | 121441 |
rs752361330 | snp | G/T | 1.65258e-05 | 0.00287448 | missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96917721 | TAAAATCAAAAAGAG[G/T]TCATCGATCTCTTAA | 121441 |
rs752374734 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96946649 | AGATACTAAGGATAC[A/G]TCAAATGATCTGCCA | 121441 |
rs752397350 | snp | A/G | 1.66382e-05 | 0.00288424 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942675 | AAAGTGAATTGTATT[A/G]TCTATGCTGTGTAAC | 121441 |
rs752452245 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96908211 | GGCTTTTAGTAGCAC[C/T]GTATCGGATGAATGG | 121441 |
rs752551738 | in-del | -/A | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96909904 | GCAATAGTATCCTTT[-/A]AAAAAAAAAAAACAC | 121441 |
rs752570154 | in-del | -/TT | 0.00853486 | 0.0647656 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912826 | TGAAGGGGTAAGTGA[-/TT]TTTTTTTTTTTTAAA | 121441 |
rs752606732 | snp | A/G | 3.55973e-05 | 0.0042187 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936566 | TAAGCTAATATACCT[A/G]TACACACTAACATTT | 121441 |
rs752681445 | snp | A/G | 1.6574e-05 | 0.00287867 | missense | NEDD1 | GRCh38.p7 | 12:96951474 | TTTGCAAGTGGAGAT[A/G]ATTAAACAGTTTCAT | 121441 |
rs752694718 | snp | A/G | 1.65236e-05 | 0.00287429 | missense, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96909796 | GCTTCATCAGGAGAT[A/G]ATATTAAAATATGGG | 121441 |
rs752696725 | snp | C/T | 1.65529e-05 | 0.00287683 | missense | NEDD1 | GRCh38.p7 | 12:96936640 | TAGTGGCTGACACTC[C/T]TCTAACTGCGGTAGA | 121441 |
rs752771086 | snp | A/C | | | downstream-variant-500B | NEDD1 | GRCh38.p7 | 12:96953749 | GAGAGATTTACCTTC[A/C]CACCTGAAATTAAAA | 121441 |
rs752944992 | snp | C/T | 4.96956e-05 | 0.00498451 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96940467 | AGACAGTGGAAAAAA[C/T]CAGGATTTCTCCAGC | 121441 |
rs752995742 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96934161 | CAGATTCAAACAAAT[A/G]TATCAAAATATCTAA | 121441 |
rs753023113 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96926027 | ATAATATACTTTCAA[A/G]GGGATTTTTTTTTTT | 121441 |
rs753035632 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96927247 | TAGTGTCTTAGTGAA[A/G]GTGATAGGAATGTGG | 121441 |
rs753112802 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96913975 | ATTTTTATCAATCCT[C/T]TCCTAAAGGTATCCA | 121441 |
rs753178961 | in-del | -/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96944492 | TCCAGTTCTCTTTTT[-/C]TTTTTCTTCTTCTAT | 121441 |
rs753197383 | in-del | -/A | 1.90217e-05 | 0.00308391 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951924 | AAATATCAATAATTT[-/A]AAAAGCATTTTCCTG | 121441 |
rs753306174 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96925423 | CTAACTTGTGAGGTA[C/T]ATGTTCTCATTTTAC | 121441 |
rs753326749 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96933655 | GCCAGGTGACTAATA[A/C]CTCCTTTTTGTTTTT | 121441 |
rs753437906 | snp | A/G | 1.65231e-05 | 0.00287424 | missense | NEDD1 | GRCh38.p7 | 12:96943665 | TTAATGTTTTTATGG[A/G]ATCTCCAGGGAAAGA | 121441 |
rs753509299 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96934752 | TAGGTTGGGCAGGCT[G/T]GTCTTGAACGCCTGA | 121441 |
rs753516112 | snp | C/T | 1.67775e-05 | 0.00289629 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943537 | AGGACACCATATGCA[C/T]ATGCAGTTTTTCCCT | 121441 |
rs753532603 | snp | C/G | 1.76899e-05 | 0.00297399 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936573 | ATATACCTGTACACA[C/G]TAACATTTCTACACA | 121441 |
rs753537875 | snp | A/T | 1.65438e-05 | 0.00287605 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96936647 | TGACACTCCTCTAAC[A/T]GCGGTAGATTTCATG | 121441 |
rs753583914 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96946799 | AAATTTTGTTTGTTC[A/G]TGTAATAGCAGCCAA | 121441 |
rs753630054 | in-del | -/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96907871 | GGTAGGTGGGCAGAT[-/G]GTCCTCTTCCCCGCC | 121441 |
rs753638609 | in-del | -/T | 3.70226e-05 | 0.00430232 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935252 | AACAAATAGCTATTA[-/T]TTCCATTAACAGGCA | 121441 |
rs753641544 | in-del | -/C | 3.57788e-05 | 0.00422944 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917598 | GTTAAATTAAGGTAA[-/C]TTTTTTTTTTTTTTT | 121441 |
rs753707792 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96947843 | GGTGAAGACGTACAG[A/T]CAGTGCCTCTTGGTT | 121441 |
rs753786682 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96920293 | AATTCATACTAGATT[A/G]TGGTGCTTATATAAA | 121441 |
rs753819859 | snp | A/T | 1.67217e-05 | 0.00289147 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942555 | CACTAGTTTTAAAAT[A/T]TGATTTTCTAATTTG | 121441 |
rs753931076 | snp | A/C | 1.65151e-05 | 0.00287355 | missense | NEDD1 | GRCh38.p7 | 12:96934985 | TTATAGTCTGTTCGG[A/C]ACTTGAAGTACTCCT | 121441 |
rs754088042 | in-del | -/TGTGTGTGTG | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96923795 | ATACCTGTTTGTGTG[-/TGTGTGTGTG]TGTGTGTGTGTGTGT | 121441 |
rs754089326 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96928941 | GTGATCTGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 121441 |
rs754125271 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96938916 | TCACTTCCGGCCAGG[A/T]TGCTTTTAGGCAATT | 121441 |
rs754179431 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96927367 | CTGAATTAAAGTTAT[C/T]AGCTTTATGTGGATC | 121441 |
rs754183609 | snp | G/T | 0.000103504 | 0.00719313 | intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96907629 | GCATTTTACAGGTTA[G/T]CCTCACTTGAGCTGT | 121441 |
rs754212263 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96914133 | TAGAATGTCTCTGGT[C/T]GATAAAGGCAGACTG | 121441 |
rs754241010 | snp | G/T | 1.7864e-05 | 0.00298859 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944843 | TGTTTGATTGAAAAA[G/T]CATCCCCATTATTTA | 121441 |
rs754307653 | snp | C/T | 1.65359e-05 | 0.00287536 | missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96917733 | GAGTTCATCGATCTC[C/T]TAAGGTAAGCAATTT | 121441 |
rs754349416 | snp | A/G | 1.65108e-05 | 0.00287317 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96937362 | GACATCAGCTATGGG[A/G]AAAGGAACAGTTGCT | 121441 |
rs754380181 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96950630 | CTCAAAAACATGCAC[A/C]ATGAAAACATTGACT | 121441 |
rs754412491 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96915036 | TAGCAAACTGTCCTG[A/C]TTTGCAGTGACAACC | 121441 |
rs754474896 | snp | A/G | 1.65138e-05 | 0.00287343 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96936773 | TCACAAGACATCTGT[A/G]CAGTGTATAGCATTT | 121441 |
rs754504506 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96920785 | TTTCAATTTTTACTT[A/G]ATTGTAATCTCTTTG | 121441 |
rs754582954 | snp | C/T | 0.000186432 | 0.00965303 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951529 | TTTATTTTAATATTT[C/T]AAATGAAAGTAGAGT | 121441 |
rs754590401 | snp | A/C/G | 4.94567e-05 | 0.00497255 | synonymous-codon, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96912772 | CAAAATAGTTGTCTC[A/C/G]AGTTGCAAATGTAAA | 121441 |
rs754606590 | snp | A/G | 5.33499e-05 | 0.00516451 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917593 | GCTCTGTTAAATTAA[A/G]GTAACTTTTTTTTTT | 121441 |
rs754740436 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96929987 | TCCTTGTTATTCCTT[C/T]TACTTCCTTCTGCAC | 121441 |
rs754740555 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96945379 | AGTCTTGGTTTATCT[A/G]GTTTATGGTGCAGCT | 121441 |
rs754742381 | snp | C/T | 1.65545e-05 | 0.00287697 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96940503 | TGATACTGGGAAAAG[C/T]AGTTTAGGTGACATG | 121441 |
rs754776747 | snp | C/T | 3.38364e-05 | 0.00411303 | missense | NEDD1 | GRCh38.p7 | 12:96952039 | GAAAACAAAAGATTA[C/T]GGGCCCACTTTTGAA | 121441 |
rs754830263 | snp | A/G | 1.6522e-05 | 0.00287414 | missense | NEDD1 | GRCh38.p7 | 12:96942594 | GCTGTAGTTAACAAG[A/G]GAAGTGATGAGTCCA | 121441 |
rs754855019 | snp | C/G | 1.64779e-05 | 0.00287031 | missense | NEDD1 | GRCh38.p7 | 12:96935105 | GACAGTGTACACAAA[C/G]CTCCAGCGTCAGGCA | 121441 |
rs754863126 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96931353 | AACTTCTGACAAAAA[C/G]CAAGGCAAAAATTCA | 121441 |
rs754872911 | snp | C/G | 0.000164902 | 0.00907876 | missense | NEDD1 | GRCh38.p7 | 12:96934998 | GGCACTTGAAGTACT[C/G]CTTGTTTAAGAAATC | 121441 |
rs754885884 | in-del | -/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96935309 | TTAGTGTCCAGGGGT[-/C]CTAAAGTTTGTACAG | 121441 |
rs754920208 | in-del | -/AT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96923349 | CTTTTTTTAAGATAC[-/AT]ATGTTTTTATTTATT | 121441 |
rs755018130 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96915347 | AAGATTAGCATGTTT[A/G]TAGTATTTGAACGTG | 121441 |
rs755018857 | in-del | -/C | 0.00018245 | 0.00954943 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951427 | GTATTTTACATTCTT[-/C]CTAGAGAAGCATGCC | 121441 |
rs755080161 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96917761 | TTTAAAAAAAATCTT[C/T]ATGAAAAAATGGATA | 121441 |
rs755090158 | snp | C/G | 1.65061e-05 | 0.00287277 | missense | NEDD1 | GRCh38.p7 | 12:96945786 | ACCGGCAAAATGCAC[C/G]ATTGACTTCCATTCA | 121441 |
rs755093842 | snp | A/G | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952343 | TAAGAGAAGAAAATT[A/G]TGCATAAAAATTGGT | 121441 |
rs755171811 | snp | A/G | 3.32646e-05 | 0.00407814 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937409 | GTAAATGTTGCTTAT[A/G]TATTGTTGGAGGGTT | 121441 |
rs755181799 | snp | C/T | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953537 | ATCTATTAATATTTT[C/T]CTGTTGCTTTTTTAA | 121441 |
rs755183328 | snp | A/G | 1.73294e-05 | 0.00294353 | intron-variant | NEDD1 | GRCh38.p7 | 12:96920160 | AGAGTAAAATTGGTA[A/G]GATAGATTTTGAATT | 121441 |
rs755190334 | snp | C/G | 2.02476e-05 | 0.00318173 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940380 | ATTTAGATGTAATAA[C/G]ATTGATTTTTATATC | 121441 |
rs755190766 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96939941 | ACTGCAAGTCAGGGA[A/G]GAAAAGTAACATTAA | 121441 |
rs755220369 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96932164 | TGGTATAAGAAAAAA[C/T]AGCATTGCTGCTTAT | 121441 |
rs755232218 | in-del | -/ACACACACACACAC | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930169 | AAAACACACACACAC[-/ACACACACACACAC]ACACACACACACACA | 121441 |
rs755241866 | in-del | -/AAAA | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953224 | TAAAAAAAAAAAAAC[-/AAAA]AACAAACCTTTAGCT | 121441 |
rs755296093 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96925895 | CTGATGTAGATTTAC[G/T]TGGTAAGTCCCACAT | 121441 |
rs755297964 | snp | A/G | 0.000499958 | 0.0158028 | missense | NEDD1 | GRCh38.p7 | 12:96943715 | CTAACAGCTGAGTCT[A/G]AGAAAATATATATGG | 121441 |
rs755375335 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96947113 | GATTTAATTGTTTTT[A/G]TTGTGCTCTGGTTAC | 121441 |
rs755384576 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96923798 | CCTGTTTGTGTGTGT[G/T]TGTGTGTGTGTGTGT | 121441 |
rs755394077 | snp | A/C | 1.6517e-05 | 0.00287372 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96936695 | GGCTATTGGATCTTC[A/C]CGGGGGAAAATATAT | 121441 |
rs755466764 | snp | C/T | 2.8416e-05 | 0.00376924 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944634 | TATTTATTTTAAATA[C/T]AAAGTTAGCAAAGTT | 121441 |
rs755529964 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96911192 | TCTATTTTTAGATTT[G/T]CATTATGTTTAGAGC | 121441 |
rs755588470 | snp | C/T | 1.74488e-05 | 0.00295366 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952062 | CTTTTGAAATTTCAG[C/T]GAATACCTTAATGTT | 121441 |
rs755596406 | in-del | -/CACTG | 2.50294e-05 | 0.00353752 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937432 | GAGGGTTGGTTTGTT[-/CACTG]TTTTTTTTGTTTTTT | 121441 |
rs755638361 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930467 | AGATGTGCTTAACCC[C/G]TTCCAGGACCAAATT | 121441 |
rs755638889 | snp | A/C/G | 5.56316e-05 | 0.00527383 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951927 | TATCAATAATTTAAA[A/C/G]AGCATTTTCCTGTTT | 121441 |
rs755642905 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96908248 | AGGAAGCACATGAGT[G/T]AATTACATTAACTTT | 121441 |
rs755651567 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96945464 | CCCTCTGTCATGTGG[C/T]ATTACATTAGACAGC | 121441 |
rs755652667 | in-del | -/ACAC | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96929569 | TATACACACACACAC[-/ACAC]ACACACACACACACA | 121441 |
rs755676156 | snp | A/G | 1.65211e-05 | 0.00287407 | missense | NEDD1 | GRCh38.p7 | 12:96942604 | ACAAGGGAAGTGATG[A/G]GTCCATAGGCAAAGG | 121441 |
rs755767876 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96909507 | ATGGGGGCCAGGACA[C/T]GTAAGGCAGGCTAAG | 121441 |
rs755836628 | in-del | -/AAAAA | 0.00205067 | 0.0319551 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909905 | GCAATAGTATCCTTT[-/AAAAA]AAAAAAACACACACA | 121441 |
rs755869609 | snp | C/T | 1.64781e-05 | 0.00287033 | missense | NEDD1 | GRCh38.p7 | 12:96935115 | ACAAAGCTCCAGCGT[C/T]AGGCATCTGTTTTTC | 121441 |
rs755908856 | snp | C/T | 1.68692e-05 | 0.00290419 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943526 | TCCAAAATTGGAGGA[C/T]ACCATATGCACATGC | 121441 |
rs755915934 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96931683 | TTTAGGTAAATTAGT[A/G]TACTCATGCATTCAT | 121441 |
rs755922947 | in-del | -/A | 1.90138e-05 | 0.00308326 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912840 | ATTTTTTTTTTTTTT[-/A]AACTTTTAAAAATCT | 121441 |
rs755936932 | in-del | -/AA | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96950509 | AACAGGAAAATAGAT[-/AA]ACACCAGTACAAACT | 121441 |
rs755957451 | snp | G/T | 1.89737e-05 | 0.00308002 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909710 | TTTGAGTATGTCTAT[G/T]CTTAAATGTTTTTAA | 121441 |
rs755992805 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96946739 | TAATGTGAATTAATT[C/G]ATTTGGGATCAGTAG | 121441 |
rs756071617 | snp | G/T | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952500 | TTAAAATGGCAATTG[G/T]TGTTTCTAAGCCATT | 121441 |
rs756082665 | snp | C/G | 1.72967e-05 | 0.00294076 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945682 | AATATTTTCTTCATT[C/G]TTTATTTTAGATCCA | 121441 |
rs756186744 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96918729 | TAGGTTCTTAGTAAA[C/T]GTTTGCTGAATGACT | 121441 |
rs756230115 | snp | C/T | 1.91331e-05 | 0.00309292 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940387 | TGTAATAACATTGAT[C/T]TTTATATCTAATTCC | 121441 |
rs756318008 | snp | C/T | 0.000186933 | 0.00966601 | intron-variant | NEDD1 | GRCh38.p7 | 12:96924820 | ATTACTTTTTCTTTA[C/T]TGCGTTGACTAGGCT | 121441 |
rs756348400 | snp | A/C/G | 6.60857e-05 | 0.00574798 | missense | NEDD1 | GRCh38.p7 | 12:96934983 | TTTTATAGTCTGTTC[A/C/G]GCACTTGAAGTACTC | 121441 |
rs756362623 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96926096 | CCTACCATTTGGTAA[G/T]AGGTCAGTGGATGTT | 121441 |
rs756362643 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96942679 | TGAATTGTATTATCT[A/G]TGCTGTGTAACAAAT | 121441 |
rs756370852 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96934307 | GATGAATTAATGTAG[A/G]TAATCTCAATGTATT | 121441 |
rs756373262 | in-del | -/AAA | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96909905 | GCAATAGTATCCTTT[-/AAA]AAAAAAAAACACACA | 121441 |
rs756452015 | snp | A/C | 1.78624e-05 | 0.00298846 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96944653 | GTTAGCAAAGTTGGT[A/C]ACATCTGGTGCTGAA | 121441 |
rs756464124 | in-del | -/AAAACAAAAGAT | 3.35976e-05 | 0.0040985 | cds-indel | NEDD1 | GRCh38.p7 | 12:96952025 | AAAGACTACGAGAAG[-/AAAACAAAAGAT]TACGGGCCCACTTTT | 121441 |
rs756500791 | snp | A/T | 1.65203e-05 | 0.002874 | missense | NEDD1 | GRCh38.p7 | 12:96936786 | GTGCAGTGTATAGCA[A/T]TTCAGTACTCCACTG | 121441 |
rs756512357 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96913289 | AGCCTCCCCCATACT[C/G]TCCTTAAACAGGTTG | 121441 |
rs756512687 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96911251 | AAGGTAGCAATTTGT[A/G]GTAAGATTATTTTTT | 121441 |
rs756540167 | snp | C/T | 1.66109e-05 | 0.00288187 | stop-gained | NEDD1 | GRCh38.p7 | 12:96944753 | AATGAAATTGAAGCC[C/T]AGTTGATATGTGAAC | 121441 |
rs756549983 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96917239 | ATTTTTAGCATTTTT[A/G]AGCTGGGGATTGATT | 121441 |
rs756557056 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96927290 | TCTGCATCATACTGA[A/G]TTGTATATATTGAAA | 121441 |
rs756608618 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96949295 | AATACAGTTTTTACT[A/G]TAATTGAAAGTAGAA | 121441 |
rs756674772 | snp | A/G | 1.66463e-05 | 0.00288494 | missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96917622 | TTTTTTTTAAATAGC[A/G]AAAGCAGACATGTGT | 121441 |
rs756799906 | snp | A/G | 4.9611e-05 | 0.00498026 | missense, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96909836 | CTATGACATTGGTGG[A/G]TAAATTCAACCCACA | 121441 |
rs756800932 | snp | C/T | 3.48912e-05 | 0.00417665 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936582 | TACACACTAACATTT[C/T]TACACATACTTTGTT | 121441 |
rs756894340 | snp | C/T | 1.6654e-05 | 0.00288561 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943550 | CACATGCAGTTTTTC[C/T]CTTTTCCAGGCTTTG | 121441 |
rs756920664 | snp | A/C | 1.65261e-05 | 0.0028745 | missense | NEDD1 | GRCh38.p7 | 12:96943670 | GTTTTTATGGGATCT[A/C]CAGGGAAAGAGGAAA | 121441 |
rs756930935 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96947874 | TTGCTGCCCTGTGCT[G/T]CATGTCTGCACCTAG | 121441 |
rs756932203 | snp | G/T | 1.65395e-05 | 0.00287567 | missense, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96909835 | TCTATGACATTGGTG[G/T]ATAAATTCAACCCAC | 121441 |
rs756951660 | in-del | -/AATG | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96944953 | AGTGTTACTAAAGAC[-/AATG]AAATGGATATGAATC | 121441 |
rs757013189 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96917901 | TTAGCCAAAAACTTA[C/T]TTTTATGTCTTTTTT | 121441 |
rs757045227 | snp | C/T | 4.96225e-05 | 0.00498084 | missense | NEDD1 | GRCh38.p7 | 12:96936649 | ACACTCCTCTAACTG[C/T]GGTAGATTTCATGCC | 121441 |
rs757070256 | in-del | -/AT | 1.65143e-05 | 0.00287348 | frameshift-variant | NEDD1 | GRCh38.p7 | 12:96936705 | TCTTCCCGGGGGAAA[-/AT]ATATCAATATGATTT | 121441 |
rs757090425 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96934761 | CAGGCTGGTCTTGAA[C/T]GCCTGACCTCAGATG | 121441 |
rs757135391 | snp | A/C | 3.4057e-05 | 0.00412642 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909919 | TAAAAAAAAAAAACA[A/C]ACACACACACACACA | 121441 |
rs757149978 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96941513 | AAGAGAAGTCGAACT[A/G]CATCAAACTACATTG | 121441 |
rs757210539 | snp | G/T | 1.64939e-05 | 0.0028717 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937425 | TATTGTTGGAGGGTT[G/T]GTTTGTTTTTTTTTT | 121441 |
rs757254484 | snp | A/C | 1.65124e-05 | 0.00287331 | missense | NEDD1 | GRCh38.p7 | 12:96934986 | TATAGTCTGTTCGGC[A/C]CTTGAAGTACTCCTT | 121441 |
rs757360921 | snp | A/G | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906047 | TGTATTATTATATAT[A/G]TTTTCATATAGTCTA | 121441 |
rs757390454 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96939148 | GTTCAGAAAAAAATT[A/C]TGTTGCTTCTATTGA | 121441 |
rs757502529 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96912920 | TAAAGGTTTTTAAAA[A/G]CATTATTTTTAACTT | 121441 |
rs757519601 | in-del | -/TC | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96921674 | GGATTTTTTTTTTTC[-/TC]TTTCTTAGAGAGTCT | 121441 |
rs757525169 | snp | C/T | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906888 | ATAGTGCATTGTAAG[C/T]TCCACAAGGCCAAGG | 121441 |
rs757540039 | snp | A/G | 5.61109e-05 | 0.00529644 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945650 | TGTTTGATGTCTCTC[A/G]GTCCAAGTTGACTAT | 121441 |
rs757596274 | snp | A/G | 1.65723e-05 | 0.00287852 | missense | NEDD1 | GRCh38.p7 | 12:96937237 | AATAAGCCCACAACA[A/G]TGAACAAACGAAGTG | 121441 |
rs757686497 | snp | A/C | 0.00732786 | 0.0600852 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96937308 | AATTGTCAGAGAAGC[A/C]CCTGCCACGTCCATT | 121441 |
rs757704584 | snp | A/G | 1.65564e-05 | 0.00287714 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917742 | GATCTCTTAAGGTAA[A/G]CAATTTAAAAAAAAT | 121441 |
rs757934585 | snp | C/T | 1.69951e-05 | 0.00291501 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909925 | AAAAAAACACACACA[C/T]ACACACACAAACCGC | 121441 |
rs757956727 | snp | C/G | 1.65817e-05 | 0.00287933 | missense | NEDD1 | GRCh38.p7 | 12:96943697 | GAAAATGAAAACCGT[C/G]ATCTAACAGCTGAGT | 121441 |
rs757986341 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96948241 | CCCTCCTGTTACACT[C/T]GTCCCTACTTTTTTT | 121441 |
rs758033517 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96950149 | ATGAAAAAGCATTTC[A/G]AGGAAGAGGAATGGT | 121441 |
rs758069132 | snp | A/C | 1.65075e-05 | 0.00287289 | missense | NEDD1 | GRCh38.p7 | 12:96936762 | ACCATCAGTGCTCAC[A/C]AGACATCTGTGCAGT | 121441 |
rs758079177 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96936285 | CCAGAGCCCCTGTTT[G/T]TGGCGTAATAGACAG | 121441 |
rs758079277 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96919178 | TGTGAACTCAGTTTG[C/T]TTAAAACCTGAAAGT | 121441 |
rs758095784 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96934527 | TAAGACAGAGTTGGG[-/T]TTTTTTTGTTTTGTT | 121441 |
rs758103005 | snp | A/G | 3.30011e-05 | 0.00406195 | synonymous-codon, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96912742 | CTTTTTAGTAACAGC[A/G]TCTTCCAGTGGCGAC | 121441 |
rs758168534 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96942989 | GAGCCGGTGAACAAG[A/G]GAATTCGAGAGGGCA | 121441 |
rs758174719 | snp | A/G | 3.33862e-05 | 0.00408558 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951387 | GAATGACCTAGAATT[A/G]GTTAAACTATTGTAA | 121441 |
rs758193257 | snp | C/T | 1.71882e-05 | 0.00293152 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951506 | TGCAACTGGTATGTA[C/T]GGCAAATTTTATTTT | 121441 |
rs758218672 | snp | A/G | 6.62175e-05 | 0.00575364 | missense | NEDD1 | GRCh38.p7 | 12:96940487 | ATTTCTCCAGCTTTG[A/G]TGATACTGGGAAAAG | 121441 |
rs758225562 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96933896 | AAAATTCAGTTAGTT[C/T]TAGTCTAAGATCAGT | 121441 |
rs758247349 | in-del | -/A | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96913018 | AATAGTTTTGAATAT[-/A]GGGGAACAATTGAAG | 121441 |
rs758293475 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96944171 | AATTTAATTTTTTAT[A/G]TAAGGGTTCAAAATG | 121441 |
rs758407535 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96914344 | TTTTAAAGTATAAAA[A/G]TAACAGATGGTATTT | 121441 |
rs758421721 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96929930 | TCTGTGAATACCTTT[C/T]GGCTGTTATGGGCTG | 121441 |
rs758486568 | in-del | -/TTT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96917599 | TTAAATTAAGGTAAC[-/TTT]TTTTTTTTTTTTTAA | 121441 |
rs758497116 | snp | A/G | 1.65184e-05 | 0.00287384 | missense | NEDD1 | GRCh38.p7 | 12:96945756 | CAGAAAAAATAGCCG[A/G]CAGCATTGGAAATAA | 121441 |
rs758501691 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96931273 | TTTCTAAGCATAAAT[A/G]TAAAGAAGTATAGTT | 121441 |
rs758507495 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96912310 | GTGGATGTTTGCTTC[C/G]TAGTTTAGATTGTTA | 121441 |
rs758507793 | snp | A/C | 3.68277e-05 | 0.00429098 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945661 | TCTCAGTCCAAGTTG[A/C]CTATTAATATTTTCT | 121441 |
rs758551094 | snp | A/G | 6.60906e-05 | 0.00574812 | synonymous-codon, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96909789 | CAGATTTGCTTCATC[A/G]GGAGATGATATTAAA | 121441 |
rs758579906 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96950963 | CTGAAAGTACATTTT[C/T]TCAATAGCTAAACTG | 121441 |
rs758619917 | in-del | -/TAGGGAG | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96948208 | TGTGCATCTGTATCT[-/TAGGGAG]TAGGGAGTCTCCCTC | 121441 |
rs758662449 | snp | A/G | 1.65866e-05 | 0.00287976 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937397 | AAGAAAAAGCAGGTA[A/G]ATGTTGCTTATATAT | 121441 |
rs758728443 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96922532 | GCTTATTGTATCTTG[A/C]TAGAGAGTTTTCTTA | 121441 |
rs758736290 | snp | A/T | 1.65908e-05 | 0.00288012 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917757 | GCAATTTAAAAAAAA[A/T]CTTCATGAAAAAATG | 121441 |
rs758748215 | snp | A/G | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952222 | ATCTTAAAAATATGT[A/G]TATTTTTATATTAAA | 121441 |
rs758941625 | snp | C/T | 1.65776e-05 | 0.00287898 | missense | NEDD1 | GRCh38.p7 | 12:96944745 | AGCCAGAGAATGAAA[C/T]TGAAGCCCAGTTGAT | 121441 |
rs758995136 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96914977 | TTGATCTTCAATGGA[A/C]ACCATCTTTTTCTAT | 121441 |
rs759012482 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96951767 | TAAATTTTCCAAATA[C/T]ACTAATTTCACCAAC | 121441 |
rs759057360 | in-del | -/A | 3.32588e-05 | 0.00407778 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917749 | TAAGGTAAGCAATTT[-/A]AAAAAAATCTTCATG | 121441 |
rs759078232 | in-del | -/T | 0.0119892 | 0.076491 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912826 | TGAAGGGGTAAGTGA[-/T]TTTTTTTTTTTTTAA | 121441 |
rs759079031 | in-del | -/CTT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96951690 | CTGAGATACTTAAGC[-/CTT]CTTTTTTCCATGGCT | 121441 |
rs759100466 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96950503 | AAATATTAACAGGAA[A/G]ATAGATACACCAGTA | 121441 |
rs759132000 | snp | A/C/T | 3.29828e-05 | 0.00406085 | missense | NEDD1 | GRCh38.p7 | 12:96937342 | ACAGTTCTACCACAA[A/C/T]CTATGACATCAGCTA | 121441 |
rs759145924 | snp | C/G | 0.000208124 | 0.0101989 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944814 | AGTACATGAAACTTC[C/G]TGATGTTTGAAAGTG | 121441 |
rs759159821 | snp | C/T | 1.64914e-05 | 0.00287149 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96937290 | AGGAGTTCAGAATTC[C/T]GGAATTGTCAGAGAA | 121441 |
rs759171005 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96929993 | TTATTCCTTCTACTT[A/C]CTTCTGCACAGACAC | 121441 |
rs759238590 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96925035 | TTACATCATTTAGCT[A/C]CTATAATTCATATTT | 121441 |
rs759252964 | snp | A/C | 3.56392e-05 | 0.00422118 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940397 | TTGATTTTTATATCT[A/C]ATTCCTATAAGGTTT | 121441 |
rs759284518 | snp | A/G | 1.65173e-05 | 0.00287374 | missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96917696 | AATAACACTGTTAAT[A/G]TTTGGGATTTAAAAT | 121441 |
rs759390888 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96909271 | GCTAAGTCCCTTACC[A/G]GGTAAGGAAGGGACT | 121441 |
rs759414929 | snp | G/T | 0.000166353 | 0.00911861 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942670 | AATGAAAAGTGAATT[G/T]TATTATCTATGCTGT | 121441 |
rs759425188 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96946487 | GATTACCGTAAGCAA[C/G]AATGTTGGAGAAAAT | 121441 |
rs759478137 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96933000 | TCATTATCTTTAGCC[-/T]TTTTTTTTTTTTTTT | 121441 |
rs759496769 | snp | G/T | 1.84544e-05 | 0.00303758 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935250 | AGTAACAAATAGCTA[G/T]TATTCCATTAACAGG | 121441 |
rs759511411 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96909108 | TTGAACCTGGAAGGC[A/G]GAGGTTGTGGTGAGC | 121441 |
rs759521745 | in-del | -/CTAT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96924452 | ATGAACATGGTATAA[-/CTAT]CTATTTATCTAAGCC | 121441 |
rs759537103 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96945524 | ATTAGAAATAATGTT[A/G]TAGAAAGTTTCTAAG | 121441 |
rs759603279 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96934452 | GTCCACTGAATGACA[A/C]CGTGGTTGTCATGAT | 121441 |
rs759623268 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96932744 | ATGGTTGAATGGTGG[A/G]TACATAAGCAATGAT | 121441 |
rs759650234 | snp | C/G | 4.98533e-05 | 0.00499241 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912703 | ATGGATTGTTTGATG[C/G]TCCATAACTCCTCAT | 121441 |
rs759724821 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96918570 | GGTTTTCTGTCTTTT[C/G]GGTGTGAAATTCGTA | 121441 |
rs759730007 | in-del | -/ATTA | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96933619 | TTAATGGGTTAACAT[-/ATTA]ATTGTCTTAACTTAG | 121441 |
rs759752235 | snp | A/T | 1.80876e-05 | 0.00300724 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912828 | AAGGGGTAAGTGATT[A/T]TTTTTTTTTTTAAAC | 121441 |
rs759759868 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96945870 | AATTGAGAAACTACT[C/T]CTTCTATCTAGACCT | 121441 |
rs759774469 | snp | A/G | 1.65531e-05 | 0.00287686 | missense | NEDD1 | GRCh38.p7 | 12:96951443 | CTAGAGAAGCATGCC[A/G]TAGGGACATTGTGAA | 121441 |
rs759944894 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96942426 | ATGTAAAAGAGAAAT[G/T]TAAATCAGTATTCTC | 121441 |
rs759956083 | snp | C/T | 1.64779e-05 | 0.00287031 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96935038 | CAGTGTTTCGGATAA[C/T]GGAATAGTAACTCTC | 121441 |
rs759972578 | snp | C/G | 0.000103493 | 0.00719276 | utr-variant-5-prime, intron-variant | NEDD1 | GRCh38.p7 | 12:96907567 | TCCACAAGTCTGTCT[C/G]CTTTTTTGTCAACCT | 121441 |
rs760003299 | in-del | -/CTCTCTCTCA | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96938827 | TCTCTCATTCTCTCT[-/CTCTCTCTCA]CTCTCTCTCACACAC | 121441 |
rs760029047 | snp | C/G/T | 3.34942e-05 | 0.00409221 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940560 | TGTTCAGAGGATCCT[C/G/T]TTCTCTTGCTGGTAG | 121441 |
rs760165283 | in-del | -/A | 0.00405393 | 0.044839 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944595 | ATGGGTAATATGAGT[-/A]AAAAAATTGTATATT | 121441 |
rs760200118 | snp | C/T | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952982 | TTATATTATTGGCCT[C/T]ACCATAAAATTATTT | 121441 |
rs760332205 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96911743 | GTCAAGGAAAGGGAA[A/G]TGGTTTTTCTCGCTA | 121441 |
rs760420190 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96926832 | TCTCTACAAAAAATA[A/C]AAAAATTAGCCAGGT | 121441 |
rs760437750 | in-del | -/AA | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96911741 | AAGTCAAGGAAAGGG[-/AA]ATGGTTTTTCTCGCT | 121441 |
rs760446781 | snp | A/G | 1.65119e-05 | 0.00287327 | missense | NEDD1 | GRCh38.p7 | 12:96943653 | ATTCTAGTCCTCTTA[A/G]TGTTTTTATGGGATC | 121441 |
rs760481629 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96914563 | TTTTACTAGTAATGT[G/T]TACAGAAACATATTA | 121441 |
rs760539178 | snp | C/T | 1.6552e-05 | 0.00287676 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96936641 | AGTGGCTGACACTCC[C/T]CTAACTGCGGTAGAT | 121441 |
rs760649419 | in-del | -/AA | 0.000188377 | 0.00970325 | intron-variant | NEDD1 | GRCh38.p7 | 12:96924795 | TATTTCCTAATCTTT[-/AA]ATATATGTTATTACT | 121441 |
rs760778024 | snp | A/G | 1.66288e-05 | 0.00288343 | missense | NEDD1 | GRCh38.p7 | 12:96951490 | ATTAAACAGTTTCAT[A/G]TGCAACTGGTATGTA | 121441 |
rs760875905 | snp | A/G | 1.65616e-05 | 0.00287759 | missense | NEDD1 | GRCh38.p7 | 12:96940471 | AGTGGAAAAAATCAG[A/G]ATTTCTCCAGCTTTG | 121441 |
rs760929650 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96921213 | TTGAGGCGGAGTCTC[A/G]CTCAGCTGCCCAGGC | 121441 |
rs761009009 | snp | C/G | 1.64779e-05 | 0.00287031 | missense | NEDD1 | GRCh38.p7 | 12:96935067 | TCTGGGATGTAAATA[C/G]TCAGAGTCCATACCA | 121441 |
rs761115029 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96944939 | ACTTCTGTTGTGTGA[A/G]TGTTACTAAAGACAA | 121441 |
rs761116824 | snp | A/C | 1.64895e-05 | 0.00287132 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96937300 | AATTCCGGAATTGTC[A/C]GAGAAGCACCTGCCA | 121441 |
rs761116934 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96928830 | TAGCTGCGACTACAG[A/G]CGCCTGCTACCACGC | 121441 |
rs761141300 | in-del | -/A | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96933909 | TTTTAGTCTAAGATC[-/A]GTTTATTCAAACTAG | 121441 |
rs761172246 | snp | A/G | 0.000207039 | 0.0101724 | utr-variant-5-prime, intron-variant | NEDD1 | GRCh38.p7 | 12:96907585 | TTTTTGTCAACCTCA[A/G]GTACTTTTCTTTTGG | 121441 |
rs761214301 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96946177 | CCTGCAGTATGTTCA[C/T]AGATCTATTAGGTAT | 121441 |
rs761237283 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96942208 | CCCATTTTATAGATG[C/G]AGAAACTGAAACTTA | 121441 |
rs761289851 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96913986 | TCCTCTCCTAAAGGT[A/G]TCCAGTGGGATTGAC | 121441 |
rs761313226 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930821 | TTCTACATACACATA[C/T]ACACACATACATGCA | 121441 |
rs761317935 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96925594 | AAAAGCTTCTGGAAA[C/G]TTTACACTATTTTCT | 121441 |
rs761365260 | snp | A/G | 5.0363e-05 | 0.00501787 | missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96920114 | ACTCCTTTTGGCCAT[A/G]GTAGTAACCAGGTAC | 121441 |
rs761403497 | snp | C/T | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906376 | AGAATTTTCCAATTA[C/T]CTGCAATATGAATGC | 121441 |
rs761450553 | in-del | -/GCTTATAA | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96934936 | AATGTCCTTATGAAT[-/GCTTATAA]GCTTATAATTACATA | 121441 |
rs761496020 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96928284 | CATAATTTTTAATGA[C/G]TGGATGTATTTCATT | 121441 |
rs761505135 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96918380 | TTGATCTTAAAATTA[A/T]TTTTTGTCTTAAAAA | 121441 |
rs761529766 | in-del | -/C | 1.73231e-05 | 0.002943 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944813 | AAGTACATGAAACTT[-/C]CTGATGTTTGAAAGT | 121441 |
rs761572664 | snp | C/G | 1.65064e-05 | 0.00287279 | missense | NEDD1 | GRCh38.p7 | 12:96936746 | GAAATCACCAGTTAA[C/G]ACCATCAGTGCTCAC | 121441 |
rs761590676 | snp | C/T | 1.6549e-05 | 0.0028765 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912716 | TGCTCCATAACTCCT[C/T]ATTTAGATAACTTTT | 121441 |
rs761620497 | in-del | -/GTTT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96919049 | TAGATACAGGGCTTA[-/GTTT]GTTTGTATTATTGAG | 121441 |
rs761697812 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96950221 | AGAACTAAAAATGCA[A/G]TGAGATACCGTGTCA | 121441 |
rs761745800 | snp | C/T | 5.41903e-05 | 0.00520502 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936835 | ATTTTCTTTTCAGCA[C/T]TTTTTATTTTATTAA | 121441 |
rs761755016 | snp | A/C | 1.65828e-05 | 0.00287943 | missense | NEDD1 | GRCh38.p7 | 12:96944703 | CTCCATCATCTAACC[A/C]AACAAGAAATTCTGA | 121441 |
rs761835850 | snp | C/T | 9.61881e-05 | 0.00693432 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912846 | TTTTTTTTTAAACTT[C/T]TAAAAATCTTAGTTT | 121441 |
rs761852624 | snp | A/G | 1.65952e-05 | 0.00288051 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942659 | ATTTTCGTGAAAATG[A/G]AAAGTGAATTGTATT | 121441 |
rs761878864 | snp | C/T | 1.76437e-05 | 0.00297011 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935237 | TATTTCTTAATTTAG[C/T]AACAAATAGCTATTA | 121441 |
rs761891852 | snp | C/G | 6.59816e-05 | 0.00574338 | missense | NEDD1 | GRCh38.p7 | 12:96937279 | GCTGCTAGTGGAGGA[C/G]TTCAGAATTCCGGAA | 121441 |
rs761893291 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96945114 | AAAATGTCTTTTTCT[C/T]TTTCATATTAAAGTC | 121441 |
rs761919330 | snp | A/G | 1.66399e-05 | 0.00288438 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942565 | AAAATTTGATTTTCT[A/G]ATTTGTTATAGATGC | 121441 |
rs762009920 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96908843 | AGGAATGTTTCAAGA[C/T]TCTGGTGTGGGGAGA | 121441 |
rs762151454 | snp | A/G | 1.65304e-05 | 0.00287488 | missense, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96909769 | GCAGTCATGCAGGAA[A/G]ACCTCAGATTTGCTT | 121441 |
rs762156153 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96941147 | TCTAGAGGGTAATTT[G/T]ACAGAGTTAATATAT | 121441 |
rs762167068 | snp | C/T | 1.65181e-05 | 0.00287381 | missense | NEDD1 | GRCh38.p7 | 12:96945834 | ACATGATACAGGAAA[C/T]GTTGGATGACTTTAG | 121441 |
rs762180041 | in-del | -/CCATTAAAACAGAATACATG | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96926400 | CTTCAATAAGTTATA[-/CCATTAAAACAGAATACATG]GGCTAGGAAATGCAA | 121441 |
rs762257710 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96915128 | AGAATTACAGCAACT[A/G]TACTGAAACATTGAT | 121441 |
rs762275917 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930851 | ACACACACGTACACA[C/T]GCACTCACAGTATTG | 121441 |
rs762303415 | snp | C/T | 1.65211e-05 | 0.00287407 | missense | NEDD1 | GRCh38.p7 | 12:96945750 | CACTCTCAGAAAAAA[C/T]AGCCGACAGCATTGG | 121441 |
rs762306620 | snp | A/G | 1.69441e-05 | 0.00291063 | missense, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96909895 | TGTTGGAGCAGCAAT[A/G]GTATCCTTTAAAAAA | 121441 |
rs762340377 | snp | G/T | 1.69023e-05 | 0.00290704 | intron-variant | NEDD1 | GRCh38.p7 | 12:96919977 | TTACTTTCATTTCTC[G/T]CTTTCAGGATCATAA | 121441 |
rs762341102 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96949136 | CTCGGTTTCTTCTCC[A/G]CACTGTGGAATCAGC | 121441 |
rs762366234 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96951210 | GACCTGTAATAATTG[C/T]ATCTACTTGTGAAGA | 121441 |
rs762434680 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96913804 | AAGATATGGTAGTTG[A/G]TAGCTTTTTTTTTTA | 121441 |
rs762454041 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96917121 | CTCCTTAACGGAGAT[A/T]TGCTGGAAGACTTAG | 121441 |
rs762458046 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96926744 | ACACCTGGAATCCCA[C/G]CACTTTGGGAGGCCA | 121441 |
rs762469469 | snp | A/T | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953065 | ATCTACCTACTATGA[A/T]CTACAATTTTAGGTT | 121441 |
rs762551700 | in-del | -/ACACAC | 0.0006906 | 0.0185694 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909916 | CTTTAAAAAAAAAAA[-/ACACAC]ACACACACACACAAA | 121441 |
rs762587776 | in-del | -/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96923634 | TGTGAAGTGACTGTT[-/C]CAAGTCTGTTGCCCA | 121441 |
rs762620267 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96950291 | TAAGTCTTGATGATA[C/T]AGAGCAAGAAGAACT | 121441 |
rs762633302 | snp | A/T | 1.65655e-05 | 0.00287793 | missense | NEDD1 | GRCh38.p7 | 12:96944723 | AGAAATTCTGAGAAA[A/T]TTGAAAAGCCAGAGA | 121441 |
rs762633892 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96914852 | GTTGCATTAATAATA[C/G]ATTATCATAAAAAAG | 121441 |
rs762708441 | snp | G/T | 2.14241e-05 | 0.00327285 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912867 | ATCTTAGTTTTGCTT[G/T]ACTGGCAATTGCTTA | 121441 |
rs762729578 | snp | A/T | 1.98916e-05 | 0.00315363 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936850 | TTTTTTATTTTATTA[A/T]ATAAATCTAACTCAG | 121441 |
rs762824150 | snp | A/G | 3.35199e-05 | 0.00409376 | missense | NEDD1 | GRCh38.p7 | 12:96952019 | AAATTGAAAGACTAC[A/G]AGAAGAAAACAAAAG | 121441 |
rs762830423 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96921590 | GAAGATGTATAATAA[A/G]TATTTGAATGTATGA | 121441 |
rs762839568 | snp | A/T | | | intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96907750 | GCTGTCCCTAAACCC[A/T]GGCCGACGTTACCGC | 121441 |
rs762844089 | snp | C/T | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906607 | CCCTTCAAAAGAATT[C/T]CCAAACAGATGATGT | 121441 |
rs763014919 | in-del | -/TCTT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96919625 | TTCATTCACAGTAGC[-/TCTT]TCTCTTTCCTCTGAC | 121441 |
rs763065844 | snp | A/G | 3.3117e-05 | 0.00406908 | missense | NEDD1 | GRCh38.p7 | 12:96936636 | ACTTTAGTGGCTGAC[A/G]CTCCTCTAACTGCGG | 121441 |
rs763077394 | snp | A/C | 6.70815e-05 | 0.00579105 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909911 | GTATCCTTTAAAAAA[A/C]AAAAACACACACACA | 121441 |
rs763136870 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96932674 | CAGAAATAATTGGAG[A/T]CATTTAAAGAATTCA | 121441 |
rs763250033 | snp | A/G | 3.35435e-05 | 0.0040952 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912675 | TTATAATAGTCTAGT[A/G]CTATAGATGTTCATG | 121441 |
rs763284796 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96915090 | CCTCAACTAAAGTCA[A/G]TTCCTAGAATGGTAT | 121441 |
rs763306525 | in-del | -/A | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96909907 | AATAGTATCCTTTAA[-/A]AAAAAAAAACACACA | 121441 |
rs763313384 | in-del | -/CTT | 0.00014934 | 0.0086399 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945871 | ATTGAGAAACTACTC[-/CTT]CTATCTAGACCTTAC | 121441 |
rs763381319 | snp | C/T | 8.5714e-05 | 0.00654597 | intron-variant | NEDD1 | GRCh38.p7 | 12:96920144 | CAGTATGAGTTTATT[C/T]AGAGTAAAATTGGTA | 121441 |
rs763382775 | snp | A/G | 1.6522e-05 | 0.00287414 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96945838 | GATACAGGAAACGTT[A/G]GATGACTTTAGGTAG | 121441 |
rs763390496 | snp | A/C/G | 3.41054e-05 | 0.00412938 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934951 | TGCTTATAATTACAT[A/C/G]AAATTTATTCTTTCA | 121441 |
rs763471417 | snp | C/T | 1.65952e-05 | 0.00288051 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951424 | AAAGTATTTTACATT[C/T]TTCCTAGAGAAGCAT | 121441 |
rs763590951 | snp | A/G | 3.30006e-05 | 0.00406192 | missense | NEDD1 | GRCh38.p7 | 12:96937357 | CCTATGACATCAGCT[A/G]TGGGGAAAGGAACAG | 121441 |
rs763635879 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96933474 | ACATTCATGTAGTTT[A/T]TTTTTTCTTGAATAT | 121441 |
rs763740920 | in-del | -/TCTTAT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96911997 | CTCTCAAAATCAGAC[-/TCTTAT]TCTTAGTTATATTAT | 121441 |
rs763760521 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96925409 | TTTAATCTTTGCTAC[C/T]AACTTGTGAGGTATA | 121441 |
rs763840053 | in-del | -/TAAATTAAGG | 1.80448e-05 | 0.00300368 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917585 | AGCTCTGGGCTCTGT[-/TAAATTAAGG]TAACTTTTTTTTTTT | 121441 |
rs763878658 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96935916 | TGGAGTATGAATGTT[A/G]CTACAAGGGAAGGTC | 121441 |
rs763946954 | snp | A/G | 1.65225e-05 | 0.00287419 | missense | NEDD1 | GRCh38.p7 | 12:96943664 | CTTAATGTTTTTATG[A/G]GATCTCCAGGGAAAG | 121441 |
rs763961604 | snp | A/G | 1.65496e-05 | 0.00287655 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96936644 | GGCTGACACTCCTCT[A/G]ACTGCGGTAGATTTC | 121441 |
rs764012324 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96911755 | GAAATGGTTTTTCTC[A/G]CTATGGTAATATCTA | 121441 |
rs764013387 | snp | C/T | 1.65542e-05 | 0.00287695 | missense | NEDD1 | GRCh38.p7 | 12:96940483 | CAGGATTTCTCCAGC[C/T]TTGATGATACTGGGA | 121441 |
rs764121741 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96934730 | TTTAATAAAGATGGG[C/G]TTTCACTAGGTTGGG | 121441 |
rs764141036 | snp | A/C | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905939 | ATTACGTCTATATAC[A/C]CAAATACAGTGCTTA | 121441 |
rs764144744 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96920250 | TATTTTTAAATGGTA[A/G]TGTTTTAAAATATTC | 121441 |
rs764254818 | snp | C/G | 3.36134e-05 | 0.00409946 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942542 | ATGGTTTCTTTTTCA[C/G]TAGTTTTAAAATTTG | 121441 |
rs764265769 | snp | G/T | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906951 | AGGCTAAACCATCAC[G/T]GTACACTCAAGAGTC | 121441 |
rs764307110 | in-del | -/GCATAG | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96925325 | GCAGAGGTTATCACA[-/GCATAG]AATGCTTACCACCAT | 121441 |
rs764413399 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96942821 | CTGCTTCAATCAGGA[C/T]GTCAACCAGAGCTTC | 121441 |
rs764452619 | snp | C/G | 1.64779e-05 | 0.00287031 | missense | NEDD1 | GRCh38.p7 | 12:96935092 | ATACCATAACTTTGA[C/G]AGTGTACACAAAGCT | 121441 |
rs764508583 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96919506 | TTGTTTTTCCCACTC[C/G]TCCATTTTGCAATGT | 121441 |
rs764527033 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96914105 | TTAACCTGACTTAAG[C/T]AGAATCAAGGCATAG | 121441 |
rs764562663 | snp | C/T | 1.65784e-05 | 0.00287905 | missense, utr-variant-5-prime, intron-variant | NEDD1 | GRCh38.p7 | 12:96909755 | AACTATTTGTAGGCG[C/T]AGTCATGCAGGAAAA | 121441 |
rs764576816 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96950587 | TTATTTCTTAAATAT[A/G]AGCTATATGGTACCC | 121441 |
rs764591970 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96914991 | ACACCATCTTTTTCT[A/G]TTTTATTTAAAGGCT | 121441 |
rs764633919 | snp | A/T | 1.65408e-05 | 0.00287578 | missense | NEDD1 | GRCh38.p7 | 12:96945731 | ACTGCTGGAGTTGCC[A/T]GTTCACTCTCAGAAA | 121441 |
rs764634123 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | NEDD1 | GRCh38.p7 | 12:96937303 | TCCGGAATTGTCAGA[A/G]AAGCACCTGCCACGT | 121441 |
rs764697598 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96948580 | GTTTGTTTTCGTTAT[A/T]AGAGTTGAGAAATTA | 121441 |
rs764704908 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96911837 | GCTCTGTTTACAAAA[C/T]ACCTGAAAGTTATAC | 121441 |
rs764715373 | snp | C/G | 5.07241e-05 | 0.00503582 | missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96920123 | GGCCATGGTAGTAAC[C/G]AGGTACAGTATGAGT | 121441 |
rs764718326 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930825 | ACATACACATACACA[C/G]ACATACATGCACACA | 121441 |
rs764795481 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96911153 | TATTTTAAAGAGAGC[A/G]ACAAGTATATGAAGT | 121441 |
rs764881961 | in-del | -/GAAG | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96940793 | CCACAAAAGTTTCTT[-/GAAG]GAAGTTTTTACCTTC | 121441 |
rs764957951 | snp | A/G | 1.88127e-05 | 0.00306692 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936841 | TTTTCAGCATTTTTT[A/G]TTTTATTAAATAAAT | 121441 |
rs764989937 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96946572 | TATATTTTTAAATGT[C/T]GAAAAATACTTTTTA | 121441 |
rs765017769 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96921520 | ACATTATTGGTGGAA[C/T]CATGGCCTGTTTCTT | 121441 |
rs765036407 | in-del | -/CT | 1.65359e-05 | 0.00287536 | frameshift-variant | NEDD1 | GRCh38.p7 | 12:96945737 | GGAGTTGCCAGTTCA[-/CT]CTCAGAAAAAATAGC | 121441 |
rs765072565 | in-del | -/CA | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96913352 | TTTAAATGAAGCTCT[-/CA]CTACGTACTGTTGCC | 121441 |
rs765077598 | snp | A/C | 1.65056e-05 | 0.00287272 | missense | NEDD1 | GRCh38.p7 | 12:96936748 | AATCACCAGTTAAGA[A/C]CATCAGTGCTCACAA | 121441 |
rs765144294 | snp | C/G/T | 3.32586e-05 | 0.0040778 | missense | NEDD1 | GRCh38.p7 | 12:96951491 | TTAAACAGTTTCATA[C/G/T]GCAACTGGTATGTAT | 121441 |
rs765159045 | snp | A/G | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906278 | TAGTTGCTGCTTGCT[A/G]TCTTTCTCCTTTTGC | 121441 |
rs765192754 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96912875 | TTGCTTGACTGGCAA[-/T]TTGCTTATTGTGGTG | 121441 |
rs765230177 | snp | C/T | 1.64779e-05 | 0.00287031 | missense | NEDD1 | GRCh38.p7 | 12:96935099 | AACTTTGACAGTGTA[C/T]ACAAAGCTCCAGCGT | 121441 |
rs765246984 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96920326 | TGATTATGTAATCAA[A/G]TAGTCACATCCTTCT | 121441 |
rs765283252 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96944013 | AAGTGTGCAAGAACA[G/T]TTTATCCCTGAATCC | 121441 |
rs765292318 | snp | C/T | 1.64874e-05 | 0.00287113 | missense | NEDD1 | GRCh38.p7 | 12:96937307 | GAATTGTCAGAGAAG[C/T]ACCTGCCACGTCCAT | 121441 |
rs765293442 | snp | G/T | | | intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96907637 | CAGGTTAGCCTCACT[G/T]GAGCTGTTGTCCTGC | 121441 |
rs765383415 | in-del | -/TCCA | 1.65389e-05 | 0.00287562 | frameshift-variant | NEDD1 | GRCh38.p7 | 12:96936795 | ATAGCATTTCAGTAC[-/TCCA]CTGTTCTTACTAAGG | 121441 |
rs765408530 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96939306 | TTCTGTTTCCTAAAG[C/T]TTCAGAGGCTGAGTT | 121441 |
rs765410888 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96929123 | TGCTTATCTTCAGTG[C/G]TTTATCATTTTTTCT | 121441 |
rs765450095 | snp | C/T | 3.30409e-05 | 0.0040644 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96945754 | CTCAGAAAAAATAGC[C/T]GACAGCATTGGAAAT | 121441 |
rs765461360 | snp | G/T | 1.65266e-05 | 0.00287455 | missense, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96909776 | TGCAGGAAAACCTCA[G/T]ATTTGCTTCATCAGG | 121441 |
rs765494664 | snp | A/T | 0.00016063 | 0.00896041 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909905 | GCAATAGTATCCTTT[A/T]AAAAAAAAAAACACA | 121441 |
rs765551770 | snp | A/G | 1.87009e-05 | 0.00305779 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945651 | GTTTGATGTCTCTCA[A/G]TCCAAGTTGACTATT | 121441 |
rs765614657 | snp | A/G | 1.6552e-05 | 0.00287676 | missense | NEDD1 | GRCh38.p7 | 12:96937382 | GAACAGTTGCTGTTC[A/G]AGAAAAAGCAGGTAA | 121441 |
rs765658337 | snp | C/G | | | missense | NEDD1 | GRCh38.p7 | 12:96937370 | CTATGGGGAAAGGAA[C/G]AGTTGCTGTTCAAGA | 121441 |
rs765666936 | snp | A/G | 8.89498e-05 | 0.00666836 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952075 | AGTGAATACCTTAAT[A/G]TTCTGTAATTTGGGA | 121441 |
rs765678393 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96917433 | AGCATTTTTGACCCC[C/G]TTAAAAGCTGTTGGA | 121441 |
rs765718570 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96939380 | TTTCTTCTTTGTAAC[A/G]ACTGAACTCTTGCTA | 121441 |
rs765736600 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96908983 | GGAGTTCGAGACCAG[A/C]CTGACCAACATGGAG | 121441 |
rs765765229 | in-del | -/GAT | 3.30453e-05 | 0.00406467 | cds-indel, intron-variant | NEDD1 | GRCh38.p7 | 12:96909793 | TTTGCTTCATCAGGA[-/GAT]GATATTAAAATATGG | 121441 |
rs765768166 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96915134 | ACAGCAACTATACTG[A/G]AACATTGATGTTGTG | 121441 |
rs765777767 | snp | G/T | 1.68476e-05 | 0.00290233 | intron-variant | NEDD1 | GRCh38.p7 | 12:96919981 | TTTCATTTCTCTCTT[G/T]CAGGATCATAAAGAT | 121441 |
rs765832736 | snp | C/T | 1.6566e-05 | 0.00287797 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96944725 | AAATTCTGAGAAATT[C/T]GAAAAGCCAGAGAAT | 121441 |
rs765844321 | snp | A/G | 0.000216022 | 0.0103906 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944608 | GTAAAAAAATTGTAT[A/G]TTAAAGTCATTATTT | 121441 |
rs765851270 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96950185 | AACACAGGAAAGATA[C/T]TCAACTTCACAATTA | 121441 |
rs765892167 | snp | G/T | 0.000141935 | 0.00842301 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937429 | GTTGGAGGGTTGGTT[G/T]GTTTTTTTTTTGTTT | 121441 |
rs765965707 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96949207 | ACCTAGTAGTCTTTC[A/G]TTTGCAAGATCATGG | 121441 |
rs765980093 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96913848 | TCTAGCAGATCTTAA[A/G]TTATTATGAATTGTC | 121441 |
rs766012682 | snp | A/G | 4.95225e-05 | 0.00497582 | missense | NEDD1 | GRCh38.p7 | 12:96936765 | ATCAGTGCTCACAAG[A/G]CATCTGTGCAGTGTA | 121441 |
rs766031594 | in-del | -/C | 0.000414164 | 0.0143844 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909917 | TTTAAAAAAAAAAAA[-/C]ACACACACACACACA | 121441 |
rs766103627 | snp | A/G | 1.71917e-05 | 0.00293182 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951507 | GCAACTGGTATGTAT[A/G]GCAAATTTTATTTTA | 121441 |
rs766165426 | snp | A/C | 2.09835e-05 | 0.00323903 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936857 | TTTTATTAAATAAAT[A/C]TAACTCAGAATATGG | 121441 |
rs766175089 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96907895 | CCCCGCCCCGCTTTA[A/G]GAGCCGAAAACAAAC | 121441 |
rs766188003 | snp | A/G | 1.67697e-05 | 0.00289561 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96952020 | AATTGAAAGACTACG[A/G]GAAGAAAACAAAAGA | 121441 |
rs766260394 | snp | C/G | 1.81447e-05 | 0.00301198 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917574 | ACCTGAAAGTCAGCT[C/G]TGGGCTCTGTTAAAT | 121441 |
rs766276945 | snp | C/G | 1.65141e-05 | 0.00287346 | synonymous-codon, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96917677 | TTTGGTAAGCGGAGG[C/G]CTAAATAACACTGTT | 121441 |
rs766294065 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96945362 | TTCGGTTTGTTTTTA[A/G]TAGTCTTGGTTTATC | 121441 |
rs766313613 | in-del | -/A | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96936332 | GTCAGAGTAATAATT[-/A]AAGAAATAGGTGCTG | 121441 |
rs766346165 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96921608 | TTTGAATGTATGAAT[A/G]TTTTTAGAGATGACA | 121441 |
rs766349377 | snp | C/T | 1.65395e-05 | 0.00287567 | missense | NEDD1 | GRCh38.p7 | 12:96942583 | TTGTTATAGATGCTG[C/T]AGTTAACAAGGGAAG | 121441 |
rs766351973 | snp | A/G | 1.6522e-05 | 0.00287414 | missense, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96909791 | GATTTGCTTCATCAG[A/G]AGATGATATTAAAAT | 121441 |
rs766413145 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96931290 | AAAGAAGTATAGTTA[C/T]AAGTCACTGGCAACA | 121441 |
rs766431246 | snp | A/C | 1.65548e-05 | 0.002877 | missense | NEDD1 | GRCh38.p7 | 12:96936639 | TTAGTGGCTGACACT[A/C]CTCTAACTGCGGTAG | 121441 |
rs766483919 | snp | A/T | 1.71953e-05 | 0.00293212 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909912 | TATCCTTTAAAAAAA[A/T]AAAACACACACACAC | 121441 |
rs766489024 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96946226 | GTAGAAAAAGATACT[G/T]TAAAGCACAATTCTG | 121441 |
rs766520471 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96912600 | CATTTTTGAAAGCTA[C/T]TCTGTAAGCTATACT | 121441 |
rs766574702 | in-del | -/TTCTT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96928413 | TCTTCTGATTTTTGA[-/TTCTT]TTCTTTGAGAGTACA | 121441 |
rs766594501 | snp | A/G | 1.6517e-05 | 0.00287372 | missense | NEDD1 | GRCh38.p7 | 12:96945759 | AAAAAATAGCCGACA[A/G]CATTGGAAATAACCG | 121441 |
rs766620628 | snp | A/G | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952266 | GTCATCTACCCAATA[A/G]GAAAGTCAACAGGAT | 121441 |
rs766644732 | snp | A/G | 4.21159e-05 | 0.0045887 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940373 | AAAATTTATTTAGAT[A/G]TAATAACATTGATTT | 121441 |
rs766664908 | snp | A/G | 3.4475e-05 | 0.00415167 | intron-variant | NEDD1 | GRCh38.p7 | 12:96920152 | GTTTATTCAGAGTAA[A/G]ATTGGTAAGATAGAT | 121441 |
rs766692600 | in-del | -/T | 0.0763445 | 0.179844 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945891 | TCTAGACCTTACTTG[-/T]TTTTTTTTTTAGATG | 121441 |
rs766710047 | snp | A/G | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953390 | TTTGTACTGAAGCAT[A/G]TAGGGATGTTAATGT | 121441 |
rs766782304 | snp | C/G | 1.66416e-05 | 0.00288453 | missense | NEDD1 | GRCh38.p7 | 12:96940430 | CTCGAAGCATAAACA[C/G]AGACACTTTATCTAA | 121441 |
rs766827606 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96941077 | CCATAATGTTTTTCT[C/T]AGTGGAATGGAGTTA | 121441 |
rs766853795 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96942262 | GTCACAAAGCTATTA[A/G]GTGGTATAGGCAGAA | 121441 |
rs766933790 | snp | C/G/T | 0.000573006 | 0.0169169 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944816 | TACATGAAACTTCCT[C/G/T]ATGTTTGAAAGTGTT | 121441 |
rs766948266 | snp | A/C | 3.29794e-05 | 0.00406061 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96937293 | AGTTCAGAATTCCGG[A/C]ATTGTCAGAGAAGCA | 121441 |
rs766962902 | in-del | -/TACT | 1.71047e-05 | 0.00292439 | intron-variant | NEDD1 | GRCh38.p7 | 12:96919959 | GATTATGGGGCAGTG[-/TACT]TACTTTCATTTCTCT | 121441 |
rs766987252 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96927901 | GTCTTTTTTATGTTA[C/T]ATAGGAGCATTGGTA | 121441 |
rs767015664 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96923198 | GTTGCATGGAATAGT[A/G]GTTCATACTGTATTA | 121441 |
rs767047707 | snp | C/T | 2.07583e-05 | 0.0032216 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937182 | CTGAGCTTTTAAATA[C/T]TCCATTACATTTCAG | 121441 |
rs767099119 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96937682 | TATTCATCCTTAATA[C/G]TACTAAAGACTGAAT | 121441 |
rs767136238 | snp | A/G | 1.64803e-05 | 0.00287052 | missense | NEDD1 | GRCh38.p7 | 12:96952040 | AAAACAAAAGATTAC[A/G]GGCCCACTTTTGAAA | 121441 |
rs767145481 | snp | C/T | 0.167244 | 0.235905 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917599 | TTAAATTAAGGTAAC[C/T]TTTTTTTTTTTTTTT | 121441 |
rs767197187 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930116 | AAATGTTGTCCGTGG[A/G]ATTTTAGTTTTTGGT | 121441 |
rs767324994 | snp | A/G | 1.66385e-05 | 0.00288426 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942672 | TGAAAAGTGAATTGT[A/G]TTATCTATGCTGTGT | 121441 |
rs767396644 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96910354 | GAGATAAAAAATTGC[C/T]CAATATCTCCATCTT | 121441 |
rs767411560 | in-del | -/AGTGAAGCTTGGGGGGGCTACT | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953082 | TACAATTTTAGGTTA[-/AGTGAAGCTTGGGGGGGCTACT]GACTTGGTTACCTTC | 121441 |
rs767411763 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96925036 | TACATCATTTAGCTC[C/G]TATAATTCATATTTA | 121441 |
rs767443399 | in-del | -/T | 0.0119892 | 0.076491 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912825 | TGAAGGGGTAAGTGA[-/T]TTTTTTTTTTTTTTA | 121441 |
rs767480249 | snp | C/T | 1.89478e-05 | 0.00307791 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935255 | CAAATAGCTATTATT[C/T]CATTAACAGGCATAT | 121441 |
rs767484542 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96909427 | TGAAAAGACACTGAG[A/G]TGAGAATGACTTTGC | 121441 |
rs767486150 | snp | C/T | 6.60371e-05 | 0.0057458 | missense | NEDD1 | GRCh38.p7 | 12:96943649 | TTGCATTCTAGTCCT[C/T]TTAATGTTTTTATGG | 121441 |
rs767491285 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96946490 | TACCGTAAGCAAGAA[A/T]GTTGGAGAAAATGTG | 121441 |
rs767574003 | snp | C/T | 1.65968e-05 | 0.00288065 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912706 | GATTGTTTGATGCTC[C/T]ATAACTCCTCATTTA | 121441 |
rs767621113 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96934577 | GAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTAC | 121441 |
rs767640001 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96945891 | ATCTAGACCTTACTT[G/T]TTTTTTTTTTAGATG | 121441 |
rs767658742 | snp | A/C | 1.65515e-05 | 0.00287671 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96951445 | AGAGAAGCATGCCAT[A/C]GGGACATTGTGAATT | 121441 |
rs767675555 | in-del | -/A | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96914399 | TTTTGTGAATATTCC[-/A]AATTAGTTGCTATGA | 121441 |
rs767827236 | snp | A/G | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905907 | GATGAAATTATATAT[A/G]TATTGCATACATACA | 121441 |
rs767879715 | snp | C/T | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953679 | AAAAATAAAATGTTA[C/T]ATGCAAAAAATAGGA | 121441 |
rs767893833 | snp | A/C | 1.65756e-05 | 0.00287881 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96940452 | TTTATCTAAGGAAAC[A/C]GACAGTGGAAAAAAT | 121441 |
rs767938010 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96927228 | TCTTTAAAAATGATC[A/G]AATTAGTGTCTTAGT | 121441 |
rs767971691 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96928778 | TGCAAGCTCCGCCTC[A/C]TGGGTTCACACCATT | 121441 |
rs767998123 | snp | C/T | 1.64779e-05 | 0.00287031 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96935059 | AGTAACTCTCTGGGA[C/T]GTAAATAGTCAGAGT | 121441 |
rs768006922 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96928509 | CCCTATTATCTTTGG[C/T]CTCAAATGTGTGACG | 121441 |
rs768050941 | in-del | -/ACACACACACACAC | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96929559 | TGTTTTCATGTATAC[-/ACACACACACACAC]ACACACACACACACA | 121441 |
rs768098057 | in-del | -/ACACACACACACACACACACAC | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930157 | ATTATCTGTTGTAAA[-/ACACACACACACACACACACAC]ACACACACACACACA | 121441 |
rs768148960 | snp | A/G | 4.95225e-05 | 0.00497582 | missense | NEDD1 | GRCh38.p7 | 12:96945824 | TTTATTCAGAACATG[A/G]TACAGGAAACGTTGG | 121441 |
rs768165247 | snp | C/T | 1.6661e-05 | 0.00288621 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951405 | TAAACTATTGTAATT[C/T]TAAAAAGTATTTTAC | 121441 |
rs768169633 | snp | C/T | 7.51889e-05 | 0.00613097 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937439 | TGGTTTGTTTTTTTT[C/T]TGTTTTTTTGTTTTT | 121441 |
rs768232644 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96926860 | GGTGTGGTGGTGCGC[A/G]CCTATAGTCCTAGCT | 121441 |
rs768232717 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96943110 | AGCAAGTTACTAGGT[C/G]CAAGCCACGTTCAAA | 121441 |
rs768255272 | snp | G/T | 6.7891e-05 | 0.00582588 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96940410 | CTAATTCCTATAAGG[G/T]TTGCCTCGAAGCATA | 121441 |
rs768278117 | snp | A/G | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905486 | TGATGGCTACTTTTG[A/G]AAATCTGTATATGTT | 121441 |
rs768304482 | in-del | -/TTAG | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96919046 | TATTAGATACAGGGC[-/TTAG]TTTGTTTGTATTATT | 121441 |
rs768315555 | snp | G/T | 1.6609e-05 | 0.0028817 | synonymous-codon, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96920095 | AACCACTAATTTATC[G/T]AGTACTCCTTTTGGC | 121441 |
rs768318121 | snp | A/G | 0.000187248 | 0.00967415 | intron-variant, missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96924892 | TTTATTTTGTCCCCA[A/G]ATTCTGGAAGAAGCA | 121441 |
rs768358839 | snp | G/T | 0.000203955 | 0.0100963 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943785 | CCTGAAAATGATACT[G/T]AACTCACTGTATGTG | 121441 |
rs768543057 | in-del | -/A | 0.00405393 | 0.044839 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944594 | ATGGGTAATATGAGT[-/A]AAAAAAATTGTATAT | 121441 |
rs768651469 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96926648 | GCTACTTAATGAATG[-/T]TTATTAATTAAAAAA | 121441 |
rs768657900 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96950074 | ATACCTGCAGTTCTC[A/C]TATAAATAACAAAGG | 121441 |
rs768677341 | snp | A/G | 3.32254e-05 | 0.00407573 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96944692 | TCTAAATACCTCTCC[A/G]TCATCTAACCAAACA | 121441 |
rs768682129 | snp | A/G | 1.66715e-05 | 0.00288712 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917766 | AAAAAATCTTCATGA[A/G]AAAATGGATATCTTA | 121441 |
rs768724864 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96922699 | AAGTGTACAGCTTGT[G/T]GAATTTTTATGTATA | 121441 |
rs768761470 | snp | C/G | 0.000182009 | 0.0095379 | missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96917655 | ATTTAAATTCTACAT[C/G]TATGTATTTGGTAAG | 121441 |
rs768798466 | snp | A/G | 0.000132646 | 0.00814281 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942650 | CTTAGAAGTATTTTC[A/G]TGAAAATGAAAAGTG | 121441 |
rs768829770 | snp | A/G | 3.29761e-05 | 0.00406041 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96937317 | AGAAGCACCTGCCAC[A/G]TCCATTGCCACAGTT | 121441 |
rs768940687 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96937899 | GATAAGCTTTCTCTT[A/C]TTGTAGAAAATATTT | 121441 |
rs769024566 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96908678 | ATAGGGACTTAGTGG[C/T]GTCTCATTTGACCAT | 121441 |
rs769030584 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96908245 | ATAAGGAAGCACATG[A/G]GTGAATTACATTAAC | 121441 |
rs769049293 | snp | A/G | 4.95217e-05 | 0.00497578 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96943603 | AGTGTTTCCTCCAAG[A/G]AAAAATCCAGTAACT | 121441 |
rs769070632 | in-del | -/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96939781 | TCTTTATTGTTGTCT[-/C]ACCTTACTATTCTTT | 121441 |
rs769085375 | in-del | -/AC | 0.494854 | 0.0504629 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909916 | CTTTAAAAAAAAAAA[-/AC]ACACACACACACACA | 121441 |
rs769118677 | in-del | -/AAT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96949944 | AATCATTAAAAATAA[-/AAT]AATGCACTGCCTATA | 121441 |
rs769132307 | snp | C/T | 1.71405e-05 | 0.00292745 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935220 | AGTAAGTGTGACATG[C/T]TTATTTCTTAATTTA | 121441 |
rs769150385 | snp | A/G | 1.66785e-05 | 0.00288773 | splice-acceptor-variant | NEDD1 | GRCh38.p7 | 12:96936610 | GTTCTCCTTTCCAAA[A/G]GCTAGTGAAAACTTT | 121441 |
rs769170285 | snp | A/G/T | 3.33819e-05 | 0.00408534 | missense | NEDD1 | GRCh38.p7 | 12:96940423 | GGTTTGCCTCGAAGC[A/G/T]TAAACACAGACACTT | 121441 |
rs769229213 | snp | A/T | 1.85679e-05 | 0.0030469 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945655 | GATGTCTCTCAGTCC[A/T]AGTTGACTATTAATA | 121441 |
rs769240392 | snp | A/G | 1.65482e-05 | 0.00287643 | missense, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96909863 | CACACACATCACCAC[A/G]TGGAATCAGCTCAAT | 121441 |
rs769252963 | in-del | -/AT | 0.000116337 | 0.00762594 | frameshift-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96917632 | ATAGCAAAAGCAGAC[-/AT]GTGTCAATTTAAATT | 121441 |
rs769302162 | snp | A/C | 2.45456e-05 | 0.00350317 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934931 | ATATCAAATGTCCTT[A/C]TGAATGCTTATAATT | 121441 |
rs769307614 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96940180 | TCTTTTGAGGAACCT[G/T]TTGTTCCATGAAAAT | 121441 |
rs769327776 | in-del | -/ATG | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96923557 | ATGTAGTGCTGTCTC[-/ATG]GTGGTTTTAATTTGC | 121441 |
rs769397432 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96910926 | GCTTTAAAATGTGAC[-/T]GGTTCAGGAACAAAA | 121441 |
rs769398414 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96913497 | TCCTGCCTCAGCCTC[A/T]CAAGTGGCAGGGATT | 121441 |
rs769410935 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96908877 | ACATTATAAGAACAA[A/T]TAAAAATTTCAGATA | 121441 |
rs769419365 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930488 | GGACCAAATTGTGAC[A/C]ACATATATGAAATGT | 121441 |
rs769505254 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96944508 | TTTTTCTTCTTCTAT[A/G]TCTCTTCCTATTTTC | 121441 |
rs769510774 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96947787 | TCAGGAGAAGTGTGT[C/G]TGTCCCACTTTCAGC | 121441 |
rs769733490 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96924389 | GATTATATTGGATCT[A/G]TGGACCAATTTAGGA | 121441 |
rs769753308 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96950273 | TAAAAAATCTGGTAA[A/T]ACTAAGTCTTGATGA | 121441 |
rs769791992 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96938835 | TTCTCTCTCTCTCTC[A/T]CACACACACACACAT | 121441 |
rs769817240 | in-del | -/A | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96926509 | TGATTTTACATACTT[-/A]ATGTTTTCCTTTTAT | 121441 |
rs769818402 | snp | A/G | 4.95037e-05 | 0.00497488 | missense | NEDD1 | GRCh38.p7 | 12:96937271 | ATGTGAATGCTGCTA[A/G]TGGAGGAGTTCAGAA | 121441 |
rs769852058 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96945952 | TTACTATTGTCTAGG[G/T]TCTGGTAATCCTAAA | 121441 |
rs769877821 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96951297 | AATAAATGCTCAGTG[C/T]ATTGGTATTTTTATT | 121441 |
rs769879530 | snp | A/G | 8.25348e-05 | 0.00642344 | missense | NEDD1 | GRCh38.p7 | 12:96943622 | AATCCAGTAACTTCA[A/G]GTACTTCAGTATTGC | 121441 |
rs769886477 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96908855 | AGACTCTGGTGTGGG[A/G]AGACAGACATTATAA | 121441 |
rs769901144 | in-del | -/A | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96948934 | CCTGCCATCTAACCC[-/A]GGGGGAGCATTGCTT | 121441 |
rs769966738 | snp | A/G | 1.67565e-05 | 0.00289447 | missense | NEDD1 | GRCh38.p7 | 12:96943727 | TCTAAGAAAATATAT[A/G]TGGGAAAACAGGAAT | 121441 |
rs770012540 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96932817 | GTGTACCTGATTCTG[A/T]ACAGAAATGCTATTT | 121441 |
rs770060687 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96940021 | AAAAAAATCACATTT[G/T]TAGATGATCATGAGT | 121441 |
rs770123166 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96932334 | TTTGGAGGCCAGGTG[C/T]GGTGGCTCACACCTG | 121441 |
rs770163663 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96935298 | TAGACCTCTGATTAG[C/T]GTCCAGGGGTCCTAA | 121441 |
rs770176589 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96933874 | TTAGTAAAAAAGAAA[A/T]GTAGATAAAATTCAG | 121441 |
rs770213277 | snp | A/G | 3.30371e-05 | 0.00406417 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96945835 | CATGATACAGGAAAC[A/G]TTGGATGACTTTAGG | 121441 |
rs770241376 | snp | A/G | 6.65247e-05 | 0.00576697 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951414 | GTAATTCTAAAAAGT[A/G]TTTTACATTCTTCCT | 121441 |
rs770262638 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96947326 | CACAGAAAGGGAGCA[C/G]TTCTTCTGTGGGGGC | 121441 |
rs770320197 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96951573 | AAAAATCCATGAAAG[A/G]TAATATATTTTAGTT | 121441 |
rs770323459 | snp | A/G | 1.64781e-05 | 0.00287033 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96935032 | ACTGGGCAGTGTTTC[A/G]GATAATGGAATAGTA | 121441 |
rs770454558 | snp | A/G | 1.65269e-05 | 0.00287457 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96942617 | TGAGTCCATAGGCAA[A/G]GGAGATGGTAAGAAC | 121441 |
rs770507945 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96911226 | TTTTCCCTCTTACTA[-/T]TATAAGAGAAAGGTA | 121441 |
rs770510166 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96940662 | TAATTTTCTCCATCC[C/T]TGGGGTGGTATCTTT | 121441 |
rs770512705 | snp | C/T | 1.8103e-05 | 0.00300852 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909728 | TAAATGTTTTTAAAA[C/T]ACATTGTTTTAAACT | 121441 |
rs770540675 | snp | A/G | 4.94662e-05 | 0.00497299 | missense | NEDD1 | GRCh38.p7 | 12:96935172 | CCATAGGCTTGGATA[A/G]AAGAATCATCCTCTA | 121441 |
rs770552198 | in-del | -/TTAA | 1.65681e-05 | 0.00287815 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917747 | CTTAAGGTAAGCAAT[-/TTAA]AAAAAATCTTCATGA | 121441 |
rs770573222 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96915899 | GTTATCATGCAGATA[A/G]CTAAAATAAGATATT | 121441 |
rs770599935 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96951624 | TAAATAGGGAGTTTT[A/G]TAGACTAAATAAGTA | 121441 |
rs770630759 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96945543 | AAAGTTTCTAAGATT[C/T]GTATTCCAGACAGTG | 121441 |
rs770649870 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96925696 | TGATAGGTTGCTGTA[A/T]TGTTAATTTTGAAAG | 121441 |
rs770661135 | snp | A/G | 3.44964e-05 | 0.00415295 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944807 | CCAAGTAAGTACATG[A/G]AACTTCCTGATGTTT | 121441 |
rs770797903 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96939159 | AATTCTGTTGCTTCT[A/G]TTGAAGTTGTCCTGA | 121441 |
rs770851702 | snp | C/T | 3.29766e-05 | 0.00406045 | missense | NEDD1 | GRCh38.p7 | 12:96937337 | TTGCCACAGTTCTAC[C/T]ACAACCTATGACATC | 121441 |
rs770920273 | snp | C/G | 1.68439e-05 | 0.00290201 | missense | NEDD1 | GRCh38.p7 | 12:96944670 | CATCTGGTGCTGAAA[C/G]TGGAAATCTAAATAC | 121441 |
rs770927109 | snp | A/G | 0.000128209 | 0.00800549 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945664 | CAGTCCAAGTTGACT[A/G]TTAATATTTTCTTCA | 121441 |
rs770930929 | in-del | -/AT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96924362 | CAAAAAATCTGCTTC[-/AT]ATTTTGATTAAGATT | 121441 |
rs770939698 | snp | A/G | 1.67047e-05 | 0.00288999 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917774 | TTCATGAAAAAATGG[A/G]TATCTTAATGCATTT | 121441 |
rs771081006 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96948533 | TCAGCTCTCGGTTGA[A/G]TTTAAAATAATATGA | 121441 |
rs771081111 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96934300 | TAACCCTGATGAATT[A/T]ATGTAGATAATCTCA | 121441 |
rs771100884 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96911504 | AGGAGTTCCCAGCCT[A/T]AGCAACTTGGGGTCC | 121441 |
rs771117247 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96926551 | TTTAAACCTTTGGAA[-/T]TTTTTTTTTTTTTCA | 121441 |
rs771168936 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96947494 | AGTTGTGAAGGTCTT[A/C]ACACACAGGTAATGG | 121441 |
rs771191182 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96910269 | TGAGTTTTTGCATCT[A/G]CATTTGGGTATTTGT | 121441 |
rs771294752 | snp | C/T | 1.64887e-05 | 0.00287125 | missense, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96912801 | AACCTGTTCCACTTT[C/T]AGAGCTTGCTGAAGG | 121441 |
rs771303053 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96919883 | AATGTTAAAGCAAAT[A/G]TTAGATTGATAAATA | 121441 |
rs771347001 | in-del | -/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96936391 | GAAGTGAATAGAAAA[-/G]GTAAGATGGAATGTT | 121441 |
rs771422000 | snp | C/T | 3.31791e-05 | 0.00407289 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951427 | GTATTTTACATTCTT[C/T]CTAGAGAAGCATGCC | 121441 |
rs771427855 | snp | C/T | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905605 | ATAGGCACAGAGGCA[C/T]GGACAAAAATGACAG | 121441 |
rs771436431 | snp | G/T | 3.4918e-05 | 0.00417825 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951939 | AAAAAGCATTTTCCT[G/T]TTTTTCTAGAATGAA | 121441 |
rs771567236 | in-del | -/CTTC | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96910389 | ATGTACTCTCCATAT[-/CTTC]CTTCCTCTCTGTGTG | 121441 |
rs771642539 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96914277 | CTATATATATGTACT[A/G]CTGTTATGCATTATG | 121441 |
rs771673901 | snp | A/G | 1.65015e-05 | 0.00287237 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96945817 | AATTCGTTTTATTCA[A/G]AACATGATACAGGAA | 121441 |
rs771684034 | in-del | -/TATC | 1.66062e-05 | 0.00288146 | frameshift-variant | NEDD1 | GRCh38.p7 | 12:96940439 | TAAACACAGACACTT[-/TATC]TAAGGAAACAGACAG | 121441 |
rs771687881 | snp | A/G | 1.69683e-05 | 0.00291271 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936595 | TTCTACACATACTTT[A/G]TTCTCCTTTCCAAAG | 121441 |
rs771718801 | snp | A/G | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952891 | TATTTTCTTTTTCCA[A/G]ATAAGAAGCTTGGAT | 121441 |
rs771739939 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96926612 | CCTGTTTTATCTGAT[G/T]GTGGCCCAAAGCATC | 121441 |
rs771750263 | snp | G/T | 2.30763e-05 | 0.00339671 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937431 | TGGAGGGTTGGTTTG[G/T]TTTTTTTTTGTTTTT | 121441 |
rs771767489 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96933583 | TCTCTTTGTACTTTA[A/G]CCATATGAAAATGGG | 121441 |
rs771769363 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96916164 | GGTAGGGCCCAAATA[A/G]TAGGACTTTGAAAGC | 121441 |
rs771770213 | in-del | -/ATGTT | 1.77887e-05 | 0.00298229 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952073 | TCAGTGAATACCTTA[-/ATGTT]CTGTAATTTGGGAAG | 121441 |
rs771770342 | snp | A/C/G | 3.30853e-05 | 0.00406716 | missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96920076 | AAATTATTTTACACA[A/C/G]TGTAACCACTAATTT | 121441 |
rs771816887 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96924510 | GTTTTTACTGTAGAG[A/G]GCTTGCATATCTTTT | 121441 |
rs771999716 | snp | C/T | 0.000186724 | 0.0096606 | intron-variant, missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96924863 | GTTGAATAGAAGTGA[C/T]GATAGTGGACATCTT | 121441 |
rs772008132 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96927743 | AGATCTGATAAATGT[A/G]AATATTAATTACATT | 121441 |
rs772092327 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96911608 | ACTTACGTTCCTCAC[C/T]TTCTCATGATTTCTA | 121441 |
rs772116924 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96934485 | AATTTGTTACCCTTT[-/T]CTTTTCTTTTCTTTT | 121441 |
rs772144068 | snp | C/T | 1.77291e-05 | 0.00297729 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912833 | GTAAGTGATTTTTTT[C/T]TTTTTTAAACTTTTA | 121441 |
rs772180050 | snp | A/T | 7.00611e-05 | 0.00591825 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936828 | GTGAGACATTTTCTT[A/T]TCAGCATTTTTTATT | 121441 |
rs772205745 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96950021 | ACATTAATAAGAACT[A/G]TTTATCACACAATAT | 121441 |
rs772211472 | snp | A/G | 0.000102904 | 0.00717225 | intron-variant | NEDD1 | GRCh38.p7 | 12:96919952 | GTTCGAGGATTATGG[A/G]GCAGTGTACTTACTT | 121441 |
rs772213553 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96936912 | GTATAGTTTTGTTTC[A/G]TAATTACATAATGAT | 121441 |
rs772224446 | snp | A/G | 1.67489e-05 | 0.00289381 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96951969 | AATGCATTCTTTGCT[A/G]GAAAGATACTCAGTG | 121441 |
rs772231055 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96948637 | TAAGTGGAAATCTGT[A/G]CATCTGTTTCTGTTG | 121441 |
rs772233941 | snp | A/C | 3.3129e-05 | 0.00406982 | missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96917649 | GTGTCAATTTAAATT[A/C]TACATCTATGTATTT | 121441 |
rs772413800 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96908594 | TTGTGAAATCACCTT[C/G]TTAGAATTACGTGTT | 121441 |
rs772447503 | snp | C/T | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906881 | GCTTCCTATAGTGCA[C/T]TGTAAGCTCCACAAG | 121441 |
rs772480190 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96921202 | TGTTTGGTTTTTTGA[C/G]GCGGAGTCTCGCTCA | 121441 |
rs772518586 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96935329 | AGTTTGTACAGTTGA[C/T]GGATCTAGTAAGAAA | 121441 |
rs772521705 | snp | G/T | | | intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96907850 | GCTCAGTTCTTAGAA[G/T]ACCGAGGTAGGTGGG | 121441 |
rs772577456 | snp | C/T | 1.65351e-05 | 0.00287528 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96942623 | CATAGGCAAAGGAGA[C/T]GGTAAGAACTACTTA | 121441 |
rs772647839 | snp | A/G | 3.46188e-05 | 0.00416032 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934947 | TGAATGCTTATAATT[A/G]CATAAAATTTATTCT | 121441 |
rs772652718 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96908944 | CACTTTGGGAGGCTG[A/G]GGCGGGCAGATCACC | 121441 |
rs772667382 | snp | A/G | 1.65116e-05 | 0.00287324 | missense | NEDD1 | GRCh38.p7 | 12:96935190 | GAATCATCCTCTATG[A/G]CACTTCAAGTAAGAA | 121441 |
rs772735431 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96928448 | AGTTCTCTTTCAATG[A/T]AATTTAGTAGCAGGC | 121441 |
rs772737741 | snp | C/T | 1.64787e-05 | 0.00287038 | missense | NEDD1 | GRCh38.p7 | 12:96935030 | CTACTGGGCAGTGTT[C/T]CGGATAATGGAATAG | 121441 |
rs772763502 | in-del | -/AACACAC | 1.76398e-05 | 0.00296978 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909915 | CCTTTAAAAAAAAAA[-/AACACAC]ACACACACACACAAA | 121441 |
rs772804232 | snp | A/G | 4.95242e-05 | 0.0049759 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96936767 | CAGTGCTCACAAGAC[A/G]TCTGTGCAGTGTATA | 121441 |
rs772845919 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96914815 | TAACCACACAATTTC[C/T]ATTAATTATTTAAGT | 121441 |
rs772847284 | in-del | -/CT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96941640 | TGGCCAGTGAGACTC[-/CT]CTGGAGGAACTTTTG | 121441 |
rs772864347 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96913690 | CCTTTTGTTTTATAA[A/G]TTAATCCCTCTGATT | 121441 |
rs772920063 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96911185 | GCTGTTCTCTATTTT[A/T]AGATTTTCATTATGT | 121441 |
rs772946735 | in-del | -/ACAC | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96909916 | CTTTAAAAAAAAAAA[-/ACAC]ACACACACACACACA | 121441 |
rs772999141 | snp | A/G | 1.65699e-05 | 0.00287831 | missense | NEDD1 | GRCh38.p7 | 12:96944720 | ACAAGAAATTCTGAG[A/G]AATTTGAAAAGCCAG | 121441 |
rs773021014 | in-del | -/TTTT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96929623 | ATATATATATATATA[-/TTTT]TTTTTTTTTTAATGG | 121441 |
rs773096901 | snp | A/G | 5.78118e-05 | 0.00537611 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936846 | AGCATTTTTTATTTT[A/G]TTAAATAAATCTAAC | 121441 |
rs773105392 | snp | A/G | | | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96937365 | ATCAGCTATGGGGAA[A/G]GGAACAGTTGCTGTT | 121441 |
rs773145781 | snp | C/T | 3.35115e-05 | 0.00409324 | stop-gained | NEDD1 | GRCh38.p7 | 12:96952018 | GAAATTGAAAGACTA[C/T]GAGAAGAAAACAAAA | 121441 |
rs773231338 | snp | A/G | 3.30131e-05 | 0.00406269 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96943630 | AACTTCAAGTACTTC[A/G]GTATTGCATTCTAGT | 121441 |
rs773256689 | snp | A/G | 3.29962e-05 | 0.00406165 | missense | NEDD1 | GRCh38.p7 | 12:96937277 | ATGCTGCTAGTGGAG[A/G]AGTTCAGAATTCCGG | 121441 |
rs773279632 | snp | A/G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96922810 | TCCAGTCACTACCTC[A/G/T]TATTTTATGAAAGGA | 121441 |
rs773298018 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96938887 | TGAGAATAGTAGACT[C/G]AGTCTCAGATCTGTC | 121441 |
rs773311406 | in-del | -/TGTG | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96926989 | GAAAAAAAAAAAAAT[-/TGTG]TGTGTGTGTGTGTGT | 121441 |
rs773361686 | snp | A/G | 1.65151e-05 | 0.00287355 | missense | NEDD1 | GRCh38.p7 | 12:96936702 | GGATCTTCCCGGGGG[A/G]AAATATATCAATATG | 121441 |
rs773393686 | snp | C/G | 3.37308e-05 | 0.00410661 | missense | NEDD1 | GRCh38.p7 | 12:96943736 | ATATATATGGGAAAA[C/G]AGGAATCTAAAGACT | 121441 |
rs773448236 | snp | C/G | 1.6571e-05 | 0.0028784 | missense | NEDD1 | GRCh38.p7 | 12:96936631 | TGAAAACTTTAGTGG[C/G]TGACACTCCTCTAAC | 121441 |
rs773529012 | in-del | -/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96923787 | CTCCTTAATACCTGT[-/G]TTGTGTGTGTGTGTG | 121441 |
rs773537914 | snp | A/G | 1.76253e-05 | 0.00296856 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909909 | TAGTATCCTTTAAAA[A/G]AAAAAAACACACACA | 121441 |
rs773544176 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96946160 | TTAAATTGGGTTCTT[A/C]ACCTGCAGTATGTTC | 121441 |
rs773574339 | snp | A/G | 2.14549e-05 | 0.0032752 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940359 | ACCTAGCTTATGATA[A/G]AATTTATTTAGATGT | 121441 |
rs773599496 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96951821 | CTAGTAAGTTGTTAA[A/G]TACAAGAAATATCAT | 121441 |
rs773631539 | snp | A/T | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96953183 | TGCCCCATTTTGACT[A/T]CTGAGATGAAAGTAT | 121441 |
rs773750487 | snp | A/G | 1.66065e-05 | 0.00288149 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951421 | TAAAAAGTATTTTAC[A/G]TTCTTCCTAGAGAAG | 121441 |
rs773754235 | snp | A/G | 1.72326e-05 | 0.0029353 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909739 | AAAATACATTGTTTT[A/G]AACTATTTGTAGGCG | 121441 |
rs773791108 | in-del | -/CACACACACAC | 1.72979e-05 | 0.00294086 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909934 | ACACACACACACACA[-/CACACACACAC]AACCGCTTATTAGGT | 121441 |
rs773856179 | snp | A/T | 1.73246e-05 | 0.00294312 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944811 | GTAAGTACATGAAAC[A/T]TCCTGATGTTTGAAA | 121441 |
rs773858957 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96914964 | GAGTCCCAATATATT[C/G]ATCTTCAATGGACAC | 121441 |
rs773864305 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96929623 | TATATATATATATAT[A/T]TTTTTTTTTTAATGG | 121441 |
rs773938333 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96951761 | CAAATATAAATTTTC[A/C]AAATATACTAATTTC | 121441 |
rs773947980 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96931937 | TAAATAATTATCTTA[A/G]TAGAGACTGAAAAAC | 121441 |
rs774041995 | snp | A/C | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952751 | GTTCATAGGACTCGA[A/C]AAGAGCTATCTGGTG | 121441 |
rs774065969 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96914043 | GTTGGAGACTGGGAC[A/C]GAGGGAACATGTGCT | 121441 |
rs774211007 | snp | A/T | 1.64914e-05 | 0.00287149 | missense | NEDD1 | GRCh38.p7 | 12:96937286 | GTGGAGGAGTTCAGA[A/T]TTCCGGAATTGTCAG | 121441 |
rs774226095 | snp | A/G | 4.95495e-05 | 0.00497718 | missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96917694 | TAAATAACACTGTTA[A/G]TATTTGGGATTTAAA | 121441 |
rs774317971 | snp | G/T | 1.67719e-05 | 0.0028958 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917780 | AAAAAATGGATATCT[G/T]AATGCATTTAGAGTA | 121441 |
rs774343458 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96947575 | TACCCATTTATTCAA[C/G]AAGCATTTGGGTGTC | 121441 |
rs774357479 | snp | A/G | 1.65105e-05 | 0.00287315 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96936713 | GGGGAAAATATATCA[A/G]TATGATTTAAGAATG | 121441 |
rs774366874 | in-del | -/CA | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96938836 | TCTCTCTCTCTCTCT[-/CA]CACACACACACATTT | 121441 |
rs774479731 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96945510 | ATAGATAAATGACTA[C/T]TAGAAATAATGTTAT | 121441 |
rs774508209 | in-del | -/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96933510 | AGAGAAAAGATTTGA[-/C]TATTCAAGTGGATAT | 121441 |
rs774520805 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96935554 | GGAAGGTTTAGAAAC[A/G]ATTGACATTTTGGGC | 121441 |
rs774526595 | snp | C/G | 3.33117e-05 | 0.00408102 | splice-donor-variant | NEDD1 | GRCh38.p7 | 12:96936813 | ACTGTTCTTACTAAG[C/G]TGAGACATTTTCTTT | 121441 |
rs774534719 | snp | C/G | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905707 | TTGGCCCTATACGCT[C/G]TGTTATGGCTCTTGA | 121441 |
rs774567626 | in-del | -/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96918407 | AAAAAGTTTTAATAT[-/G]AAAAATATAAACATA | 121441 |
rs774567723 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96948080 | CAGAGAGGGTATTGA[A/G]GACCTCTTTCTCAGC | 121441 |
rs774600757 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96918520 | GCAAAATTTGATGAT[A/T]TTTTCCATTTTCAGC | 121441 |
rs774648479 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96932891 | TTATGTAGATGAGAA[C/T]GCTGAGTTTTGGAGA | 121441 |
rs774689097 | snp | C/T | 1.67307e-05 | 0.00289224 | intron-variant | NEDD1 | GRCh38.p7 | 12:96934967 | AAATTTATTCTTTCA[C/T]TTTTATAGTCTGTTC | 121441 |
rs774724012 | snp | A/T | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905622 | GACAAAAATGACAGG[A/T]CTGTTTCAGGGCCAG | 121441 |
rs774795852 | snp | C/T | 1.65436e-05 | 0.00287602 | missense, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96909847 | GTGGATAAATTCAAC[C/T]CACACACATCACCAC | 121441 |
rs774808301 | snp | G/T | 1.728e-05 | 0.00293933 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951942 | AAGCATTTTCCTGTT[G/T]TTCTAGAATGAAATG | 121441 |
rs774810261 | snp | C/T | 1.66101e-05 | 0.0028818 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96940437 | CATAAACACAGACAC[C/T]TTATCTAAGGAAACA | 121441 |
rs774905405 | snp | G/T | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906781 | AATCCACATCCACAA[G/T]AGTTTCCCTTATTAT | 121441 |
rs774941776 | snp | A/G | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952921 | TTATTTTATTTTGTG[A/G]TCTTTATCATTAACT | 121441 |
rs774978952 | snp | A/G | 1.64776e-05 | 0.00287028 | missense | NEDD1 | GRCh38.p7 | 12:96935036 | GGCAGTGTTTCGGAT[A/G]ATGGAATAGTAACTC | 121441 |
rs775031669 | in-del | -/T | 1.68596e-05 | 0.00290336 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942531 | CCTAAATTGATATGG[-/T]TTCTTTTTCACTAGT | 121441 |
rs775280127 | snp | G/T | 2.50294e-05 | 0.00353752 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937432 | GGAGGGTTGGTTTGT[G/T]TTTTTTTTGTTTTTT | 121441 |
rs775358064 | snp | A/G | 3.65838e-05 | 0.00427675 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943779 | TATTTGCCTGAAAAT[A/G]ATACTGAACTCACTG | 121441 |
rs775439171 | in-del | -/A | 1.65414e-05 | 0.00287583 | frameshift-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96920074 | GAAATTATTTTACAC[-/A]AGTGTAACCACTAAT | 121441 |
rs775478267 | snp | G/T | 1.65102e-05 | 0.00287312 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96943651 | GCATTCTAGTCCTCT[G/T]AATGTTTTTATGGGA | 121441 |
rs775491933 | snp | A/T | 9.5574e-05 | 0.00691215 | intron-variant | NEDD1 | GRCh38.p7 | 12:96912840 | ATTTTTTTTTTTTTT[A/T]AACTTTTAAAAATCT | 121441 |
rs775503482 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96950914 | TATTTTATTGAGTAA[A/G]CCATGCTATATCCAC | 121441 |
rs775583670 | in-del | -/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96914538 | ATTTGGAAACATTGG[-/T]TTTTTTAGCTTTTAC | 121441 |
rs775674416 | snp | A/T | 8.27767e-05 | 0.00643284 | missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96917651 | GTCAATTTAAATTCT[A/T]CATCTATGTATTTGG | 121441 |
rs775682251 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96921204 | TTTGGTTTTTTGAGG[C/T]GGAGTCTCGCTCAGC | 121441 |
rs775698747 | snp | A/G | 1.65343e-05 | 0.00287521 | missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96920036 | TGGAATGATTGCTAC[A/G]TTGCTTCTGGATCTC | 121441 |
rs775728320 | in-del | -/CTCTCTCTCACA | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96938828 | TCTCTCATTCTCTCT[-/CTCTCTCTCACA]CACACACACATTTTT | 121441 |
rs775793070 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96936984 | ATATTTAGTTTTAAA[A/G]CTTTTTTTCTTTTTT | 121441 |
rs775893810 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96946143 | GACAAGTTCTGGTAA[C/G]CTTAAATTGGGTTCT | 121441 |
rs775915864 | in-del | -/TTG | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96933710 | TTTCCTAGACATTTT[-/TTG]TTGTTGTTGAGAGCT | 121441 |
rs775947296 | snp | A/G | 1.65395e-05 | 0.00287567 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942627 | GGCAAAGGAGATGGT[A/G]AGAACTACTTAGAAG | 121441 |
rs775949319 | snp | A/G | 3.29554e-05 | 0.00405914 | missense | NEDD1 | GRCh38.p7 | 12:96935064 | CTCTCTGGGATGTAA[A/G]TAGTCAGAGTCCATA | 121441 |
rs776034250 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930790 | TTTTTAAAGATAGAC[A/G]GTCTCAGGCCTGCTT | 121441 |
rs776072623 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96937440 | GGTTTGTTTTTTTTT[C/T]GTTTTTTTGTTTTTG | 121441 |
rs776080840 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96942059 | GCAAATGAATATTAC[A/G]GGATTAAAATAATCT | 121441 |
rs776124086 | snp | C/T | 1.65996e-05 | 0.00288089 | synonymous-codon, utr-variant-5-prime, intron-variant | NEDD1 | GRCh38.p7 | 12:96909753 | TAAACTATTTGTAGG[C/T]GCAGTCATGCAGGAA | 121441 |
rs776137409 | in-del | -/AC/C | 0.494854 | 0.0504629 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909915 | CTTTAAAAAAAAAAA[-/AC/C]ACACACACACACACA | 121441 |
rs776147226 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96911758 | ATGGTTTTTCTCGCT[A/C]TGGTAATATCTAGGT | 121441 |
rs776231220 | snp | A/G | 1.67685e-05 | 0.00289551 | missense | NEDD1 | GRCh38.p7 | 12:96940418 | TATAAGGTTTGCCTC[A/G]AAGCATAAACACAGA | 121441 |
rs776239056 | snp | A/G | 1.6609e-05 | 0.0028817 | missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96920096 | ACCACTAATTTATCT[A/G]GTACTCCTTTTGGCC | 121441 |
rs776328877 | snp | C/G | 0.000187635 | 0.00968412 | intron-variant, missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96924898 | TTGTCCCCAAATTCT[C/G]GAAGAAGCATTCAAT | 121441 |
rs776374759 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96945430 | AGAGGAAATGGTTCA[A/T]AGATTCTTCAAGATT | 121441 |
rs776402086 | snp | C/T | 1.65894e-05 | 0.00288 | missense | NEDD1 | GRCh38.p7 | 12:96937235 | CAAATAAGCCCACAA[C/T]AGTGAACAAACGAAG | 121441 |
rs776446157 | snp | C/T | 3.7508e-05 | 0.00433042 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943790 | AAATGATACTGAACT[C/T]ACTGTATGTGTTTAT | 121441 |
rs776501356 | snp | A/G | 1.76974e-05 | 0.00297462 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936832 | GACATTTTCTTTTCA[A/G]CATTTTTTATTTTAT | 121441 |
rs776502306 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96948888 | CAGAATACTTTCTCT[C/G]CTCTTTAGTTACTTG | 121441 |
rs776528409 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96921433 | TGATCCACCTCCCTC[A/G]GCCTCCCAAAGTGTT | 121441 |
rs776539064 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96913477 | CTCCCCAGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 121441 |
rs776569620 | in-del | -/T | 1.6651e-05 | 0.00288535 | frameshift-variant | NEDD1 | GRCh38.p7 | 12:96944687 | GGAAATCTAAATACC[-/T]CTCCATCATCTAACC | 121441 |
rs776705022 | snp | A/T | 1.66679e-05 | 0.00288681 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917767 | AAAAATCTTCATGAA[A/T]AAATGGATATCTTAA | 121441 |
rs776742203 | in-del | -/TTCAG | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96926687 | TAAGATTTCTCAAAA[-/TTCAG]TTCAGTTTAAAAATA | 121441 |
rs776768258 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96950212 | ATTAATCAGAGAACT[A/T]AAAATGCAATGAGAT | 121441 |
rs776806657 | snp | A/C/G | 3.33251e-05 | 0.00408187 | missense | NEDD1 | GRCh38.p7 | 12:96936612 | TCTCCTTTCCAAAGG[A/C/G]TAGTGAAAACTTTAG | 121441 |
rs776822144 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96908741 | GTGACTGGATTCTGA[C/T]CTGCAGAAATGCTAG | 121441 |
rs776845396 | snp | C/T | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96907038 | GCCGGAGCTCCGTCG[C/T]TGGGGCGTGGAGAGG | 121441 |
rs776887589 | snp | C/T | 4.97987e-05 | 0.00498968 | intron-variant | NEDD1 | GRCh38.p7 | 12:96942657 | GTATTTTCGTGAAAA[C/T]GAAAAGTGAATTGTA | 121441 |
rs776908930 | in-del | -/AATTTAAAA | 1.65583e-05 | 0.00287731 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917744 | TCTCTTAAGGTAAGC[-/AATTTAAAA]AAAATCTTCATGAAA | 121441 |
rs776916379 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96922702 | TGTACAGCTTGTTGA[A/G]TTTTTATGTATACGT | 121441 |
rs776981627 | snp | A/T | 1.74949e-05 | 0.00295756 | intron-variant | NEDD1 | GRCh38.p7 | 12:96935233 | TGCTTATTTCTTAAT[A/T]TAGTAACAAATAGCT | 121441 |
rs776988745 | snp | A/G | 1.65269e-05 | 0.00287457 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96945742 | TGCCAGTTCACTCTC[A/G]GAAAAAATAGCCGAC | 121441 |
rs777081387 | snp | A/G | 1.65422e-05 | 0.0028759 | synonymous-codon, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96909765 | AGGCGCAGTCATGCA[A/G]GAAAACCTCAGATTT | 121441 |
rs777151207 | in-del | -/TC | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96940223 | TAGCTCTTGTCATAT[-/TC]TGTTTTATTGTTCCA | 121441 |
rs777169302 | snp | A/G | 3.34571e-05 | 0.00408992 | missense, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96909893 | TATGTTGGAGCAGCA[A/G]TAGTATCCTTTAAAA | 121441 |
rs777283967 | snp | C/T | 0.000158975 | 0.00891417 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952070 | ATTTCAGTGAATACC[C/T]TAATGTTCTGTAATT | 121441 |
rs777292028 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96932143 | CAACATTCTTACACA[A/G]TAATGTGGTATAAGA | 121441 |
rs777375911 | snp | C/T | 1.65236e-05 | 0.00287429 | missense | NEDD1 | GRCh38.p7 | 12:96942610 | GAAGTGATGAGTCCA[C/T]AGGCAAAGGAGATGG | 121441 |
rs777449805 | snp | G/T | 1.64784e-05 | 0.00287035 | missense | NEDD1 | GRCh38.p7 | 12:96935118 | AAGCTCCAGCGTCAG[G/T]CATCTGTTTTTCTCC | 121441 |
rs777473265 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96931805 | AATACACAGAAGCAT[A/T]CATACACACAGAAAA | 121441 |
rs777491711 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96945495 | TGGCAGTTTATATAT[A/G]TAGATAAATGACTAT | 121441 |
rs777499987 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96909556 | CATTACTGTGAGGAG[A/C]CATTGGAAGGGTCAG | 121441 |
rs777514983 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96950618 | TTTTTTGTAATGCTC[A/G]AAAACATGCACAATG | 121441 |
rs777539802 | snp | C/T | 3.72849e-05 | 0.00431753 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909721 | CTATTCTTAAATGTT[C/T]TTAAAATACATTGTT | 121441 |
rs777557927 | snp | A/G | 1.65326e-05 | 0.00287507 | missense, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96909823 | TGGGATGCTTCATCT[A/G]TGACATTGGTGGATA | 121441 |
rs777592866 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96915643 | AACTAATGTGACTTC[A/G]TAGTGCATCTAAAGG | 121441 |
rs777715313 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96917854 | GGCTTCAGAATTGAA[C/G]TAAGATTTGTTAGGG | 121441 |
rs777844703 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96911474 | ACTTCCATGGAGGTT[A/G]ATTACTGAAGAACAA | 121441 |
rs777917483 | snp | C/T | 1.65042e-05 | 0.0028726 | missense | NEDD1 | GRCh38.p7 | 12:96945792 | AAAATGCACCATTGA[C/T]TTCCATTCAAATTCG | 121441 |
rs777948159 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96941460 | ATTTAAATTGCTAAG[C/T]CAAACTGAAAGAGGA | 121441 |
rs777956256 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96932819 | GTACCTGATTCTGTA[A/C]AGAAATGCTATTTAA | 121441 |
rs777981817 | in-del | -/AAAAAACACAC | 6.88705e-05 | 0.00586775 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909911 | GTATCCTTTAAAAAA[-/AAAAAACACAC]ACACACACACACAAA | 121441 |
rs777994871 | snp | C/T | 0.000186829 | 0.0096633 | intron-variant | NEDD1 | GRCh38.p7 | 12:96924823 | ACTTTTTCTTTATTG[C/T]GTTGACTAGGCTCTC | 121441 |
rs778043698 | snp | A/G | 1.65329e-05 | 0.0028751 | missense | NEDD1 | GRCh38.p7 | 12:96936793 | GTATAGCATTTCAGT[A/G]CTCCACTGTTCTTAC | 121441 |
rs778045624 | snp | C/G/T | 8.33485e-05 | 0.00645509 | missense | NEDD1 | GRCh38.p7 | 12:96944762 | GAAGCCCAGTTGATA[C/G/T]GTGAACCCCCAATCA | 121441 |
rs778131604 | snp | C/T | 1.66421e-05 | 0.00288458 | missense | NEDD1 | GRCh38.p7 | 12:96937229 | GCTGTTCAAATAAGC[C/T]CACAACAGTGAACAA | 121441 |
rs778133116 | snp | A/G | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905311 | CCAACAATGACTATG[A/G]GTATGCTTTTTTCCT | 121441 |
rs778136015 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96936458 | TCTAAGTCAAATTCT[A/G]AAATTATGCTTTAAA | 121441 |
rs778142998 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96926182 | TTACTTCTCTAAAAT[A/G]GTTTGAGCATCTTTA | 121441 |
rs778151471 | in-del | -/TTTC | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96913755 | ACTCTTTGAAAGCTA[-/TTTC]TTTCTTTTTTAAATA | 121441 |
rs778160933 | snp | C/T | 0.00013581 | 0.00823932 | missense | NEDD1 | GRCh38.p7 | 12:96944787 | CAATCAATGGATCCT[C/T]AACTCCAAGTAAGTA | 121441 |
rs778181080 | snp | A/G | 1.66269e-05 | 0.00288326 | missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96917628 | TTAAATAGCAAAAGC[A/G]GACATGTGTCAATTT | 121441 |
rs778219585 | snp | C/G | 1.64904e-05 | 0.00287139 | missense | NEDD1 | GRCh38.p7 | 12:96935175 | TAGGCTTGGATAAAA[C/G]AATCATCCTCTATGA | 121441 |
rs778222315 | snp | C/T | 1.6486e-05 | 0.00287102 | missense, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96912789 | GTTGCAAATGTAAAC[C/T]TGTTCCACTTTTAGA | 121441 |
rs778238906 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96912653 | TTAGCTTTTATAATC[A/G]CAATTCTTATAATAG | 121441 |
rs778242725 | in-del | -/ATTATTGATATTTCAC | 1.72913e-05 | 0.0029403 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952054 | GGGCCCACTTTTGAA[-/ATTATTGATATTTCAC]ATTTCAGTGAATACC | 121441 |
rs778332576 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96919746 | ATTTGTCAGAGGAAG[A/T]GAATTCTTTAAGGAA | 121441 |
rs778450875 | in-del | -/T | 0.498556 | 0.0268265 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937441 | TTTGTTTTTTTTTTG[-/T]TTTTTTTGTTTTTGG | 121441 |
rs778481332 | snp | A/G | 1.65392e-05 | 0.00287564 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96936650 | CACTCCTCTAACTGC[A/G]GTAGATTTCATGCCT | 121441 |
rs778507898 | snp | A/C | | | downstream-variant-500B | NEDD1 | GRCh38.p7 | 12:96954135 | ACAGGAAATGATTTA[A/C]AAAAATGCCTTTAGA | 121441 |
rs778508960 | snp | G/T | 1.66407e-05 | 0.00288446 | intron-variant | NEDD1 | GRCh38.p7 | 12:96943552 | CATGCAGTTTTTCCC[G/T]TTTCCAGGCTTTGAC | 121441 |
rs778517208 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96946978 | CTGTAACTTGATAGC[C/T]GCAATCCTTCTATCC | 121441 |
rs778535523 | in-del | -/GGA | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96943127 | AAGCCACGTTCAAAG[-/GGA]GGAGATTACCCAAGG | 121441 |
rs778569255 | snp | C/T | 1.69619e-05 | 0.00291216 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909921 | AAAAAAAAAAACACA[C/T]ACACACACACACAAA | 121441 |
rs778571256 | in-del | -/ACACACACACACACACACACACAC | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930159 | TATCTGTTGTAAAAC[-/ACACACACACACACACACACACAC]ACACACACACACACA | 121441 |
rs778616350 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96918985 | TGAAAAAGTTGTAAT[A/G]TAAGTGGAATATCAT | 121441 |
rs778624498 | in-del | -/CTT | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96931340 | TATAAAAATTTAAAA[-/CTT]CTGACAAAAAGCAAG | 121441 |
rs778627625 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96945040 | TAATATGTGTCTTTA[A/G]TATGGTAGAGATAGA | 121441 |
rs778637934 | in-del | -/ACACACACACACACACACACACACAC | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930157 | ATTATCTGTTGTAAA[-/ACACACACACACACACACACACACAC]ACACACACACACACA | 121441 |
rs778800811 | snp | C/T | 1.69269e-05 | 0.00290915 | intron-variant | NEDD1 | GRCh38.p7 | 12:96945899 | CTTACTTGTTTTTTT[C/T]TTAGATGTAAAACCA | 121441 |
rs778875894 | snp | A/G | 0.000103611 | 0.00719685 | intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96907655 | GCTGTTGTCCTGCAA[A/G]TAAAGTGTATTTTTG | 121441 |
rs778902701 | in-del | -/AAC | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96909915 | CCTTTAAAAAAAAAA[-/AAC]ACACACACACACACA | 121441 |
rs778958203 | snp | A/G | 1.86072e-05 | 0.00305013 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940391 | ATAACATTGATTTTT[A/G]TATCTAATTCCTATA | 121441 |
rs778971959 | snp | A/C | 1.67391e-05 | 0.00289297 | missense | NEDD1 | GRCh38.p7 | 12:96944769 | AGTTGATATGTGAAC[A/C]CCCAATCAATGGATC | 121441 |
rs779073710 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96949637 | GAAGGGGACTTATTT[G/T]TCAGATGAATACACT | 121441 |
rs779097192 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96927690 | TGAAATGTTTTATGT[A/G]TAGATTTTGTAAGCA | 121441 |
rs779164360 | snp | A/G | 1.65625e-05 | 0.00287766 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96937239 | TAAGCCCACAACAGT[A/G]AACAAACGAAGTGTT | 121441 |
rs779272606 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96917746 | TCTTAAGGTAAGCAA[C/T]TTAAAAAAAATCTTC | 121441 |
rs779306186 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96913103 | GGATCTCTGTTGCTG[C/T]TATTTTAGGACGATA | 121441 |
rs779373676 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96919869 | GTATATTTGAGGAAA[A/G]TGTTAAAGCAAATAT | 121441 |
rs779475253 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96921112 | GATTTTGTTTTTACT[A/C]TGACAATATAAACTG | 121441 |
rs779533891 | snp | C/T | 1.79146e-05 | 0.00299282 | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952079 | AATACCTTAATGTTC[C/T]GTAATTTGGGAAGTT | 121441 |
rs779573555 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96946877 | TCCATCTCTTTTTAT[C/T]CACTTCCTCTTGGCT | 121441 |
rs779622086 | snp | A/G | 1.65272e-05 | 0.0028746 | missense | NEDD1 | GRCh38.p7 | 12:96942618 | GAGTCCATAGGCAAA[A/G]GAGATGGTAAGAACT | 121441 |
rs779646995 | snp | C/G | 1.65173e-05 | 0.00287374 | missense | NEDD1 | GRCh38.p7 | 12:96936680 | TGATGGAGCCACTTT[C/G]GCTATTGGATCTTCC | 121441 |
rs779658141 | snp | A/G | 1.72234e-05 | 0.00293452 | intron-variant | NEDD1 | GRCh38.p7 | 12:96940404 | TTATATCTAATTCCT[A/G]TAAGGTTTGCCTCGA | 121441 |
rs779658606 | snp | A/T | 3.30082e-05 | 0.00406239 | missense | NEDD1 | GRCh38.p7 | 12:96945821 | CGTTTTATTCAGAAC[A/T]TGATACAGGAAACGT | 121441 |
rs779669662 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96917929 | TTTCTTACATGTGTA[A/G]CATTAATGCATATGA | 121441 |
rs779677278 | in-del | -/TGT | 3.55568e-05 | 0.0042163 | cds-indel | NEDD1 | GRCh38.p7 | 12:96952074 | CAGTGAATACCTTAA[-/TGT]TCTGTAATTTGGGAA | 121441 |
rs779700622 | snp | A/G | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96905292 | GAGAAAATTCTGTCA[A/G]TCTCCAACAATGACT | 121441 |
rs779736985 | snp | A/C | 1.64787e-05 | 0.00287038 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909935 | ACACACACACACACA[A/C]ACCGCTTATTAGGTT | 121441 |
rs779746006 | snp | A/G | 0.000560381 | 0.0167295 | intron-variant, missense, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96924872 | AAGTGATGATAGTGG[A/G]CATCTTTATTTTGTC | 121441 |
rs779763541 | snp | A/G | 6.63812e-05 | 0.00576075 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96935203 | TGACACTTCAAGTAA[A/G]AAGTAAGTGTGACAT | 121441 |
rs779775484 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96943066 | TTGGTAGTGACATCT[C/G]ACTACTTTTTCATAT | 121441 |
rs779796340 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96920641 | GGAAACTTTTTAAAA[A/G]GAAAATAAGTCAATT | 121441 |
rs779847428 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96923384 | GTAAATACTTAGGAG[A/T]GGAATTGCAGGATTG | 121441 |
rs779894560 | snp | A/G | 1.64928e-05 | 0.00287161 | missense, intron-variant, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96912749 | GTAACAGCATCTTCC[A/G]GTGGCGACAAAATAG | 121441 |
rs779927730 | snp | A/G | 1.65529e-05 | 0.00287683 | missense | NEDD1 | GRCh38.p7 | 12:96940496 | GCTTTGATGATACTG[A/G]GAAAAGTAGTTTAGG | 121441 |
rs779973331 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96944280 | TTGAAAAGATACCAT[A/G]TAAGAAGTACAAAAA | 121441 |
rs780027832 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96929941 | CTTTTGGCTGTTATG[C/G]GCTGCTTCTGTTCTC | 121441 |
rs780032338 | snp | C/T | 8.24328e-05 | 0.00641947 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96937314 | CAGAGAAGCACCTGC[C/T]ACGTCCATTGCCACA | 121441 |
rs780092017 | snp | C/T | 1.651e-05 | 0.0028731 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96934987 | ATAGTCTGTTCGGCA[C/T]TTGAAGTACTCCTTG | 121441 |
rs780126819 | snp | C/T | 1.65162e-05 | 0.00287365 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96937251 | AGTGAACAAACGAAG[C/T]GTTAATGTGAATGCT | 121441 |
rs780141330 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96950041 | TCACACAATATCACA[C/G]AGTGAAGGGATAAGA | 121441 |
rs780226950 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96914371 | ATTTACAAGTGTGAC[A/G]TAATTCTAAGAGTTT | 121441 |
rs780279981 | in-del | -/A | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96949035 | AAGACCTTGGCTCTT[-/A]ACAGCCTTGGCTACC | 121441 |
rs780480091 | snp | C/G | 4.98757e-05 | 0.00499353 | missense | NEDD1 | GRCh38.p7 | 12:96943706 | AACCGTGATCTAACA[C/G]CTGAGTCTAAGAAAA | 121441 |
rs780514870 | snp | A/G | 1.66538e-05 | 0.00288559 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951407 | AACTATTGTAATTCT[A/G]AAAAGTATTTTACAT | 121441 |
rs780614957 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96920804 | GTAATCTCTTTGGCC[A/G]TAACTATTATAAAAT | 121441 |
rs780615581 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96907955 | AAGTTGGAGCAGGTC[G/T]TTTGAACCCAGTTTT | 121441 |
rs780673796 | snp | A/G | 1.65367e-05 | 0.00287543 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96943576 | CTTTGACTTTCTACC[A/G]CAGTTGAACTCAGTG | 121441 |
rs780701392 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96924698 | ATAGTTTGGACAGTC[C/T]TGATTCTTTTGAAAG | 121441 |
rs780720909 | in-del | -/TTTT | 0.00010812 | 0.00735175 | intron-variant | NEDD1 | GRCh38.p7 | 12:96917599 | TTAAATTAAGGTAAC[-/TTTT]TTTTTTTTTTTTAAA | 121441 |
rs780765726 | snp | C/T | 1.68926e-05 | 0.0029062 | intron-variant | NEDD1 | GRCh38.p7 | 12:96936598 | TACACATACTTTGTT[C/T]TCCTTTCCAAAGGCT | 121441 |
rs780862950 | snp | C/T | 3.97235e-05 | 0.00445648 | intron-variant | NEDD1 | GRCh38.p7 | 12:96951545 | AAATGAAAGTAGAGT[C/T]GTGTGAATTTTTAAA | 121441 |
rs780875743 | snp | C/T | 1.65787e-05 | 0.00287907 | missense | NEDD1 | GRCh38.p7 | 12:96940517 | GTAGTTTAGGTGACA[C/T]GTTCTCACCTATCAG | 121441 |
rs780902090 | snp | A/C | 1.64819e-05 | 0.00287066 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96935017 | GTTTAAGAAATCACT[A/C]CTGGGCAGTGTTTCG | 121441 |
rs780902184 | snp | A/G | 1.65214e-05 | 0.0028741 | missense | NEDD1 | GRCh38.p7 | 12:96942598 | TAGTTAACAAGGGAA[A/G]TGATGAGTCCATAGG | 121441 |
rs780902921 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96945441 | TTCATAGATTCTTCA[A/C]GATTAATCCCTCTGT | 121441 |
rs780983875 | snp | C/T | 1.64787e-05 | 0.00287038 | missense | NEDD1 | GRCh38.p7 | 12:96935112 | TACACAAAGCTCCAG[C/T]GTCAGGCATCTGTTT | 121441 |
rs780992780 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96921340 | GCACCCACCATCATG[C/G]CCAGCTAATTTTTGT | 121441 |
rs781016736 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930028 | ACCATGAAGGACTTA[C/T]GGCTGTTAATTGTTT | 121441 |
rs781023150 | snp | A/G | | | upstream-variant-2KB | NEDD1 | GRCh38.p7 | 12:96906696 | TTAGTGCAGACGCCT[A/G]CTCTTTGGGTTATTT | 121441 |
rs781090109 | in-del | -/AA | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96909905 | GCAATAGTATCCTTT[-/AA]AAAAAAAAAACACAC | 121441 |
rs781092356 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96915488 | TAGTCTTCACCTTTC[A/G]TTTCTCAAATGCAGA | 121441 |
rs781110317 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96931384 | CAAAATTTAAATGAA[A/G]TAGGGAAGGTATTTA | 121441 |
rs781141146 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96914474 | TGTTGGATAAAAGTA[A/G]GATTAGTTGAGTTCA | 121441 |
rs781150420 | snp | A/G | 1.65685e-05 | 0.00287819 | synonymous-codon, utr-variant-5-prime | NEDD1 | GRCh38.p7 | 12:96920014 | AGTAACTTGTGTAAC[A/G]TACAATTGGAATGAT | 121441 |
rs781227073 | snp | C/T | 1.90529e-05 | 0.00308643 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909705 | CTTTTTTTGAGTATG[C/T]CTATTCTTAAATGTT | 121441 |
rs781246456 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96951235 | TGAAGATATTTTAAA[C/T]GAGTTCTTACATTTA | 121441 |
rs781259068 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96923917 | TATGTCAGTCTTTTC[C/T]TTTATGTTTGTTGCT | 121441 |
rs781342056 | snp | A/G | 6.72314e-05 | 0.00579752 | missense | NEDD1 | GRCh38.p7 | 12:96944774 | ATATGTGAACCCCCA[A/G]TCAATGGATCCTCAA | 121441 |
rs781352033 | snp | A/G | 1.69479e-05 | 0.00291095 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937420 | TTATATATTGTTGGA[A/G]GGTTGGTTTGTTTTT | 121441 |
rs781360419 | snp | C/T | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952348 | GAAGAAAATTGTGCA[C/T]AAAAATTGGTTATGT | 121441 |
rs781367859 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96939969 | TAATTGAATCCTGCT[G/T]TATGTTAGGCATCGC | 121441 |
rs781445708 | snp | A/G | 2.72624e-05 | 0.00369195 | intron-variant | NEDD1 | GRCh38.p7 | 12:96944635 | ATTTATTTTAAATAT[A/G]AAGTTAGCAAAGTTG | 121441 |
rs781516305 | snp | A/G | 1.75111e-05 | 0.00295893 | intron-variant | NEDD1 | GRCh38.p7 | 12:96920173 | TAAGATAGATTTTGA[A/G]TTGTATCTTACATAA | 121441 |
rs781562465 | in-del | -/T | 1.65485e-05 | 0.00287645 | frameshift-variant | NEDD1 | GRCh38.p7 | 12:96951458 | TAGGGACATTGTGAA[-/T]TTTGCAAGTGGAGAT | 121441 |
rs781565587 | snp | A/G | 6.67802e-05 | 0.00577803 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96943720 | AGCTGAGTCTAAGAA[A/G]ATATATATGGGAAAA | 121441 |
rs781594968 | snp | A/G | 1.65138e-05 | 0.00287343 | synonymous-codon | NEDD1 | GRCh38.p7 | 12:96936776 | CAAGACATCTGTGCA[A/G]TGTATAGCATTTCAG | 121441 |
rs781652293 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96925981 | AGTTACTTAACTCTC[A/G]AGCCTCCTTTTCCTT | 121441 |
rs781657187 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96942479 | TTAGCTTTTTAAGAT[G/T]GTTAGTCTCTGAACT | 121441 |
rs781659323 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96913105 | ATCTCTGTTGCTGCT[A/G]TTTTAGGACGATATC | 121441 |
rs781718412 | in-del | -/TTTTTTTG | 0.000192317 | 0.00980416 | intron-variant | NEDD1 | GRCh38.p7 | 12:96937434 | AGGGTTGGTTTGTTT[-/TTTTTTTG]TTTTTTTGTTTTTGG | 121441 |
rs781729855 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96947214 | GTGTTAAAGAATATA[C/T]GTTTTTTTCAGGAGT | 121441 |
rs781734223 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96911215 | TTTAGAGCTTAATTT[C/T]CCCTCTTACTATATA | 121441 |
rs781763458 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96933693 | AGCATTTGGTTTCTG[C/T]ATTTCCTAGACATTT | 121441 |
rs781776318 | snp | C/T | 1.95349e-05 | 0.00312523 | intron-variant | NEDD1 | GRCh38.p7 | 12:96909940 | CACACACACAAACCG[C/T]TTATTAGGTTAAACA | 121441 |
rs796153783 | snp | C/T | | | utr-variant-3-prime | NEDD1 | GRCh38.p7 | 12:96952392 | ATCTTTTTTAACATA[C/T]ATTTTTGATTGACAA | 121441 |
rs796275384 | in-del | -/AG | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96922308 | TTTATATTTTGATAA[-/AG]AGAGACATAAAGTCT | 121441 |
rs796294297 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930213 | CACACACACACACAC[A/T]CTCTCTCTCTCTCTC | 121441 |
rs796452201 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96916788 | ACATGATCTGATTTA[C/T]ATTTTTAAAGTCCAC | 121441 |
rs796493762 | snp | A/C | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96950304 | TATAGAGCAAGAAGA[A/C]CTCTGTTATACTGGT | 121441 |
rs796554216 | snp | C/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96935932 | CTACAAGGGAAGGTC[C/G]CACTGTCAGCCTTTA | 121441 |
rs796627409 | snp | A/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96908565 | TTGCCTTCTGTTTTC[A/T]AGACTTCCTTGGTTT | 121441 |
rs796694623 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930398 | AGAGAAAAGTGCATG[G/T]GGTGAAGGCCATAGG | 121441 |
rs796745103 | in-del | -/CTCTCG | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96930235 | TCTCTCTCTCTCTCT[-/CTCTCG]CTCTCTCTCACACTC | 121441 |
rs796846096 | snp | C/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96913434 | GCTGGAGTGCAATGG[C/T]GCAATCTTAGCTCAC | 121441 |
rs796884255 | snp | A/G | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96923148 | CAAGGAATCATATGT[A/G]TCTGGTTTCTTTTAG | 121441 |
rs797012114 | snp | G/T | | | intron-variant | NEDD1 | GRCh38.p7 | 12:96921626 | TTTAGAGATGACAAA[G/T]ATTTTGTTAGGCAAA | 121441 |