SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1354 | snp | A/G | 0.139564 | 0.224285 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940274 | GAGAAGCGGGTCTCC[A/G]AACCTAGGTAATCTG | 11169 |
rs878944 | snp | A/G | 0.445592 | 0.155704 | intron-variant | WDHD1 | GRCh38.p7 | 14:54976884 | TTATCAATTTATCAC[A/G]TAATATACAAATAAA | 11169 |
rs943914 | snp | G/T | 0.432944 | 0.170387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54973350 | AGAATACTAGACATT[G/T]TCACTTACTTGTTTT | 11169 |
rs1055245 | snp | A/C | 0 | 0 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939178 | ATCTGTTTTATTATC[A/C]GAATATATAATTTTC | 11169 |
rs1064087 | snp | C/T | 0 | 0 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940035 | TTCATCTTGCTTTGT[C/T]ATTAGGTTTGATTCT | 11169 |
rs1187876 | snp | A/T | 0.497749 | 0.0334707 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028481 | TTTTTCGTTCAAGTA[A/T]CAATATCATTGGCTA | 11169 |
rs1187877 | snp | C/T | 0.481703 | 0.0938806 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028443 | GGAGATCATTTGTTT[C/T]TTGGATAGACTGGCT | 11169 |
rs1187878 | snp | A/G | 0.458315 | 0.13822 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026632 | TATGTGCAGTCAGCT[A/G]AAAATGACTCATGCG | 11169 |
rs1187879 | snp | C/T | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025171 | atgcatacacataaa[C/T]atctcaatgctttac | 11169 |
rs1187880 | snp | A/G | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024783 | actcttaaggagcat[A/G]ctgccttcaagcatc | 11169 |
rs1187881 | snp | C/T | 0.49753 | 0.0350569 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022479 | ggccaggctggtgaa[C/T]aggtttttaatgtag | 11169 |
rs1187882 | snp | C/G | 0.429238 | 0.174281 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022029 | attcaacctctagat[C/G]aggagttcatacagg | 11169 |
rs1187883 | snp | A/G | 0.49703 | 0.0384237 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021516 | tacgcctgtaatccc[A/G]cactccaccttctct | 11169 |
rs1187884 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998100 | tcagcctcccaagta[C/G]ctaggataacaggca | 11169 |
rs1187885 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | WDHD1 | GRCh38.p7 | 14:54992843 | tcactgtaaccttga[A/G]ctcctgggcttaagc | 11169 |
rs1187886 | snp | C/G | 0.105569 | 0.204058 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983057 | cgtacctcagcctcc[C/G]gagtatctgggacta | 11169 |
rs1187887 | snp | C/G | 0.103794 | 0.20279 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982670 | ATCTAATTGGTACTT[C/G]GGAGAAAAAAATCTA | 11169 |
rs1187888 | snp | A/G | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967765 | ggcatggtggcatat[A/G]tctgtagtcccagct | 11169 |
rs1187889 | snp | A/G | 0.120326 | 0.21374 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950651 | gttccgtagatgtct[A/G]ttaggtctgcttggt | 11169 |
rs1201378 | snp | A/G | 0.490836 | 0.067068 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026690 | GTTCTTTGAGAAACA[A/G]CGTTTTAGGTGCAAA | 11169 |
rs1209087 | snp | A/G | 0.498964 | 0.02274 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026502 | ATAATCGTACTTCCA[A/G]AGGAGTTGGAAAGAT | 11169 |
rs2183085 | snp | G/T | 0.481473 | 0.0944461 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005673 | AATGTCTAGAACCTC[G/T]ATGTCCTGCAAATGA | 11169 |
rs2840268 | snp | C/G | 0.481473 | 0.0944461 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005265 | GAGCAATGGTAGGTA[C/G]GTTAACATAAGATGC | 11169 |
rs2878173 | snp | C/T | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966777 | TACAGCTTAACTTTT[C/T]CCCCTATCCTTAAAA | 11169 |
rs2878174 | snp | C/T | 0.493293 | 0.0575177 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003906 | GTCTGCTCATGTCTT[C/T]GCTCATCTTTCTAAT | 11169 |
rs3074190 | in-del | -/TA | 0.483995 | 0.0880135 | intron-variant | WDHD1 | GRCh38.p7 | 14:54973040 | AATCACAGAATGATT[-/TA]TATATATATAGAACT | 11169 |
rs3783643 | snp | A/G | 0.483995 | 0.0880135 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961923 | ctcactgctacctcc[A/G]cctcctgagttcaag | 11169 |
rs3783644 | snp | A/G | 0.483053 | 0.0904792 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961998 | CATACCACCACCCTC[A/G]GCTAATTTTTGTATT | 11169 |
rs3783645 | snp | C/T | 0.402982 | 0.197728 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962114 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGCC | 11169 |
rs3783646 | snp | C/T | 0.410061 | 0.192043 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005169 | TCGGCATCCACCACA[C/T]CAATCCCACTGAGTG | 11169 |
rs3831212 | in-del | -/C | 0.498982 | 0.0225409 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026542 | GATATACTACAACTA[-/C]CATGACGGCCCGAAT | 11169 |
rs4047200 | snp | A/T | 0.48 | 0.0979796 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972591 | AAAAAAAAAAAAAAA[A/T]GCCAATGAGGCATAT | 11169 |
rs4325453 | snp | A/G | 0.469148 | 0.120308 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972600 | AAAAAATGCCAATGA[A/G]GCATATTCACTTTCA | 11169 |
rs4335711 | snp | C/G | 0.370568 | 0.219005 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004145 | AAATACCTATATATA[C/G]ACTCATCATGTAGAA | 11169 |
rs4898857 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54976731 | TATTTAAGGCTATAT[A/C]CCAAAaaataaataa | 11169 |
rs4901550 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54977198 | TGCTGGGGGTGAAGA[C/G]AGACAGCAAATAGAC | 11169 |
rs6572992 | snp | C/G | 0.482234 | 0.0925596 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950498 | acccagattcataaa[C/G]caagtccttagagac | 11169 |
rs6572993 | snp | C/T | 0.482083 | 0.0929373 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960318 | gattacaggtgcctg[C/T]caccatgcccggcta | 11169 |
rs6572994 | snp | C/G | 0.482159 | 0.0927485 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960385 | gtgttcttcaggatg[C/G]tctcaatctcctgac | 11169 |
rs6572996 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | WDHD1 | GRCh38.p7 | 14:54978339 | tataatcctagcact[C/T]tggaaggctgatgca | 11169 |
rs6572997 | snp | C/T | 0.485799 | 0.0830599 | intron-variant | WDHD1 | GRCh38.p7 | 14:55010065 | CTCAGGTGATCTGCC[C/T]GCCTTGGCCTCCCAA | 11169 |
rs7142626 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022920 | acctccacctcccgg[A/G]ttcaagtgattctcc | 11169 |
rs7143054 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54987716 | cctccgcctcccagg[A/T]tcaagcaattctcct | 11169 |
rs7145818 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993633 | caaattttctttata[C/T]acttcaaacaaaaac | 11169 |
rs7146285 | snp | C/T | 0.482083 | 0.0929373 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946151 | ATGTCACAAGTCTAC[C/T]TAGTGGCCTGCAATC | 11169 |
rs7146775 | snp | A/G | 0.140242 | 0.224618 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941039 | GTATTATTAAAAGAC[A/G]TCATCCCCTAGGTCT | 11169 |
rs7147147 | snp | G/T | 0.140242 | 0.224618 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941226 | AACAAATTCAAATTG[G/T]TTGGAGCTTCAACTC | 11169 |
rs7151097 | snp | G/T | 0.0659589 | 0.169201 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977087 | CAAAAAAATAAGGTT[G/T]TTTTTTTTTTGCCAA | 11169 |
rs7151285 | snp | C/T | 0.0182019 | 0.0936463 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941274 | TGCATCTCTGAAAGG[C/T]CCTGCATTTGGAGGC | 11169 |
rs7151670 | snp | C/G | 0.398354 | 0.201224 | intron-variant | WDHD1 | GRCh38.p7 | 14:54986041 | actggatgtgtaagt[C/G]tggagacacaaggag | 11169 |
rs7152909 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54980799 | acagagtgagactcc[A/C]cataaaaaaaaaaaa | 11169 |
rs7153937 | snp | A/G | 0.483923 | 0.0882034 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004157 | ATAGACTCATCATGT[A/G]GAAGCAAGCTTCCAA | 11169 |
rs7156068 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977641 | ACTCTTGTTCAAGTC[A/C]AGCCTGGATAACGTA | 11169 |
rs7157085 | snp | A/G | 0.484279 | 0.0872533 | intron-variant | WDHD1 | GRCh38.p7 | 14:54978028 | TGAAGAAGCAAAATT[A/G]TTCATTGCAGATGAC | 11169 |
rs7157783 | snp | A/G | 0.0752113 | 0.178743 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942316 | tctaagataattgca[A/G]tttcacatgcagttg | 11169 |
rs7158676 | snp | A/G | 0.0102561 | 0.0708723 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022168 | ggcagtcccttacta[A/G]caagatactttctga | 11169 |
rs7159141 | snp | C/T | 0.100588 | 0.200439 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004641 | TATTTTTAGTAGAGA[C/T]AGGGTTTCGCCATGT | 11169 |
rs7159232 | snp | C/T | 0.427271 | 0.176281 | intron-variant | WDHD1 | GRCh38.p7 | 14:54951721 | attttagaccaatat[C/T]cctgatgaacatcga | 11169 |
rs7159933 | snp | A/C | 0.484066 | 0.0878235 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974923 | TCTTCTGTGTTGGAC[A/C]GGACTGTCTTCTGCA | 11169 |
rs7159953 | snp | A/G | 0.442655 | 0.159323 | intron-variant | WDHD1 | GRCh38.p7 | 14:54951896 | gactaaaaccacatg[A/G]ttatctcaatagatg | 11169 |
rs7492958 | snp | A/G | 0 | 0 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940814 | GTGGTGGTAGAAATT[A/G]TGGTAGTAAATATAT | 11169 |
rs8003017 | snp | C/T | 0.0770498 | 0.180522 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948265 | aggcatcacctcacc[C/T]gggaagcgcaagggg | 11169 |
rs8004402 | snp | C/T | 0.481703 | 0.0938806 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949104 | gagcacctctccccc[C/T]ccaaaggaacgcagc | 11169 |
rs8005285 | snp | A/G | 0.0807149 | 0.183963 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966333 | gaacgagactccgtc[A/G]cacaaaaaacaacaa | 11169 |
rs8005471 | snp | C/T | 0.481856 | 0.0935034 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948983 | CAAAAAGGACATCCA[C/T]ACCAAAACCCCATGT | 11169 |
rs8006977 | snp | C/T | 0.482083 | 0.0929373 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952952 | actggatccattcct[C/T]acatcttatacaaaa | 11169 |
rs8008150 | snp | G/T | 0.4021 | 0.198407 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954718 | TTGCTATAGTATAAA[G/T]AAGttctttttgttt | 11169 |
rs8009997 | snp | G/T | 0.386313 | 0.209568 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955193 | AGAAACTTGTTGCAG[G/T]GATTGTTTTTGGAGA | 11169 |
rs8011446 | snp | C/G | 0.387453 | 0.208822 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959195 | taacatagggagacc[C/G]tgtctctacaaaaac | 11169 |
rs8012152 | snp | C/T | 0.482459 | 0.0919928 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958849 | cttgcttacccatgc[C/T]catggtttaaattgc | 11169 |
rs8012571 | snp | C/G | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025995 | CTCATACATGTTTAT[C/G]ACTGCACATATTACT | 11169 |
rs8012733 | snp | C/G | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026120 | ctggttcgctctatt[C/G]tatctgtagtcccca | 11169 |
rs8013183 | snp | G/T | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026199 | GCGACAGTGGAAGCC[G/T]TGCAATCGAGCAGTA | 11169 |
rs8013521 | snp | C/G | 0.461813 | 0.132798 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947007 | GAGATTGCACCAGTG[C/G]ACTCCAGCCTTGGTG | 11169 |
rs8013929 | snp | C/T | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026130 | CTATTCTATCTGTAG[C/T]CCCCAGCAAAAGAGA | 11169 |
rs8013950 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962430 | TAAGGTGTATTTGCG[C/T]AGATGTGTCACTTTG | 11169 |
rs8015172 | snp | A/G | 0.384785 | 0.210554 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950732 | cttattccaacactg[A/G]ccacatagttggaag | 11169 |
rs8017240 | snp | A/G | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026283 | AATATTATAGTTTAG[A/G]AATCAGAGGAAAAAA | 11169 |
rs8017273 | snp | A/G | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026341 | AAAAATAAGCAAAAA[A/G]GGAAATAGCATCACT | 11169 |
rs8017572 | snp | A/G | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026473 | AAGGGGAAAATATAT[A/G]GAGAGAAGCTCGCAT | 11169 |
rs8018350 | snp | C/T | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026397 | AACAGAACAGGCCAC[C/T]GAATTTGACAAGTAG | 11169 |
rs8018800 | snp | A/G | 0.484209 | 0.0874434 | intron-variant | WDHD1 | GRCh38.p7 | 14:54986588 | CACTCCAGCTAAAAG[A/G]TAGAGCCAACAAAAA | 11169 |
rs8019149 | snp | C/T | 0.084728 | 0.187577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948192 | ctcactagggcttgt[C/T]ggacagtgggcgcag | 11169 |
rs8019220 | snp | C/T | 0.483126 | 0.0902898 | intron-variant | WDHD1 | GRCh38.p7 | 14:54986751 | GTCTTAGCATAGTGA[C/T]GGGGACTGAAGAAAG | 11169 |
rs8019354 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | WDHD1 | GRCh38.p7 | 14:54986717 | AGCACAGAGATTATC[A/G]GTTACCTTGATAAGA | 11169 |
rs8019390 | snp | C/G | 0.443866 | 0.157848 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942366 | atcctgtgtagcctt[C/G]acccagttttcccca | 11169 |
rs8020032 | snp | A/G | 0.0034487 | 0.0413818 | missense, intron-variant | WDHD1 | GRCh38.p7 | 14:54995744 | CATTGTCATTTAGAA[A/G]ATCACCAGCATTACT | 11169 |
rs8020545 | snp | A/T | 0.443866 | 0.157848 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942352 | aataatacagaaaga[A/T]cctgtgtagccttca | 11169 |
rs8020660 | snp | C/T | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014611 | ATCTATCATAACTTG[C/T]TTTAAACTTATCTTC | 11169 |
rs8021303 | snp | A/G | 0.491936 | 0.0629843 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966231 | TAATCCTAGCTACTC[A/G]GGAGGCTGAGGCAGA | 11169 |
rs8021370 | snp | C/T | 0.370162 | 0.219229 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982075 | GCAGTGGCGCGATCT[C/T]GGCCCACTGCAAGCT | 11169 |
rs8021996 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974499 | ttttgttttgttttt[G/T]ttttttttgttATAT | 11169 |
rs8022049 | snp | C/T | 0.398894 | 0.200825 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996151 | ATATGATAAAGTCCC[C/T]ATAAAGTCTGTCATA | 11169 |
rs8022664 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018897 | gcatggtggcgcatg[C/T]ctgtaatcccagcta | 11169 |
rs9285583 | snp | C/T | 0.483418 | 0.0895317 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964717 | GCATTTGCCCGGGGG[C/T]CAGGAATGCTAAAGA | 11169 |
rs9323273 | snp | C/G | 0.081446 | 0.184634 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988369 | GGTGATAAAGACGTA[C/G]TGACAAAAATCTAGA | 11169 |
rs9323274 | snp | C/T | 0.081446 | 0.184634 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988389 | AAAAATCTAGACTAA[C/T]AGTTGGCCAAGGCTA | 11169 |
rs9323275 | snp | C/T | 0.48491 | 0.0855403 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007182 | GCAGTGAGCCGAGAT[C/T]GCACCACTGCACTCC | 11169 |
rs9671441 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55013751 | tctctacaaaaaatt[A/T]aaaaattagccaggc | 11169 |
rs9671503 | snp | C/T | 0.477937 | 0.102688 | intron-variant | WDHD1 | GRCh38.p7 | 14:54951236 | aaaagatcaataaaa[C/T]tgatagaccgctagc | 11169 |
rs9733708 | snp | C/G | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950697 | ATATGGTGCTGAGAA[C/G]AATGTAAATTCTGTT | 11169 |
rs9805952 | snp | C/T | 0.483708 | 0.088773 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994595 | gtgaaaccccatctc[C/T]actaaaaatacaaaa | 11169 |
rs9806068 | snp | A/T | 0.105546 | 0.204041 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007232 | gactccatctctaat[A/T]aaaaaaaaaaaaaaa | 11169 |
rs10129318 | snp | A/G | 0.402277 | 0.198272 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948266 | ggcatcacctcaccc[A/G]ggaagcgcaaggggt | 11169 |
rs10129802 | snp | A/G | 0.405776 | 0.195535 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948803 | gtacccctctgagac[A/G]aggcttccagaggaa | 11169 |
rs10130198 | snp | A/G | 0.0970103 | 0.197722 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996432 | ggacaacatgatgaa[A/G]cctcatctccacaaa | 11169 |
rs10139354 | snp | C/T | 0.484841 | 0.0857308 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011884 | CCCTTCAATTGTTTC[C/T]GACATTTGCTATTGT | 11169 |
rs10140164 | snp | A/G | 0.491732 | 0.0637633 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939405 | ATTCACTTGTTCTCC[A/G]AAATAAATCTGTAAA | 11169 |
rs10140189 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969269 | ctgaccttgtgatcc[A/G]cccgcctatgcctcc | 11169 |
rs10142619 | snp | C/T | 0.0970103 | 0.197722 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996543 | aggtcagggctgcag[C/T]gagccatgatctcac | 11169 |
rs10148100 | snp | A/G | 0.489259 | 0.0724914 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017492 | gtattacaggcacgc[A/G]ccacccacacctggc | 11169 |
rs10150110 | snp | G/T | 0.483636 | 0.0889627 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995292 | GGCCTTATTGATCTT[G/T]TCAAAGAACCAGCTT | 11169 |
rs10150556 | snp | C/T | 0.081446 | 0.184634 | intron-variant | WDHD1 | GRCh38.p7 | 14:54986745 | AGACCAGTCTTAGCA[C/T]AGTGACGGGGACTGA | 11169 |
rs10220439 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54989588 | GTTTTCTTACAAATA[C/T]GGATGCAAATAACAA | 11169 |
rs10400738 | snp | A/C | 0.00398564 | 0.0444627 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939337 | TGCTGCACAGATATG[A/C]GAGGCTTTAGATCAT | 11169 |
rs10628556 | in-del | -/A | 0.10237 | 0.201756 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026321 | AGCCGTCAAAAAGTT[-/A]AAAAAAAAATAAGCA | 11169 |
rs10711872 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54978586 | TGATACCCTGGCTCT[-/A]AAAAAAAAAAACCGT | 11169 |
rs10715034 | in-del | -/A | 0.497984 | 0.0316851 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988737 | TACTCTTATAATAGT[-/A]AAAAAAAAAAAAAGC | 11169 |
rs11158029 | snp | C/T | 0.403509 | 0.197319 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960660 | atgagccaccatgcc[C/T]ggctaattttttttt | 11169 |
rs11338389 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54965968 | CCTAAAAAAAAAAAA[-/A]GAAAAAAATTTTAAC | 11169 |
rs11351246 | in-del | -/G | 0.373397 | 0.217424 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009994 | CCCAGCTAATTTTTT[-/G]GTATTAGTAGAGACG | 11169 |
rs11365009 | in-del | -/A | 0.146985 | 0.227789 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977913 | CAAAGGGTTGTGTGG[-/A]AAAAAAAAAAAAGCA | 11169 |
rs11402342 | in-del | -/T | 0.483762 | 0.173885 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988232 | TGGTTTGTTTTTCCG[-/T]TTTTTTTTTCCTTTC | 11169 |
rs11404089 | in-del | -/A | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939587 | TGGAAAAAAAAAAAA[-/A]GAACACTGGAAAAAA | 11169 |
rs11623528 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54998373 | gacctcaggtgatcc[A/C]ccggcctcggcctcc | 11169 |
rs11627963 | snp | C/G | 0.20111 | 0.245173 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959829 | AAAAAACCTTtccat[C/G]tagccaataaaaatt | 11169 |
rs11628328 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54977671 | AAGGAGACCCTGTTT[C/T]TAAATAAATAAATAA | 11169 |
rs11629355 | snp | C/T | 0.258843 | 0.249844 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953955 | ggaaggggaacatca[C/T]acacttgggcctgtt | 11169 |
rs11844338 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949222 | ctaaaggaggaagtt[C/T]gaacgcatcgcaaag | 11169 |
rs11846098 | snp | A/G | 0.00479606 | 0.0487342 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962857 | GTATTGCTGTAACTA[A/G]GAGAAAATAATATTA | 11169 |
rs11846514 | snp | A/C | 0.433382 | 0.169915 | intron-variant | WDHD1 | GRCh38.p7 | 14:54973622 | ATCTCTATTTACAAG[A/C]ATCACTACTTTACTA | 11169 |
rs11846854 | snp | A/G | 0.0991586 | 0.199366 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026307 | GAAAAAATTGTTTTA[A/G]GCCGTCAAAAAGTTA | 11169 |
rs11846990 | snp | C/T | 0.0944967 | 0.195752 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017478 | ctcccaagtagctag[C/T]attacaggcacgcac | 11169 |
rs11847317 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014296 | ggtgtccctacgttg[C/T]ccaggctggtcttga | 11169 |
rs11848698 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016006 | acccagccccgatgg[C/G]cttcttggtgtatca | 11169 |
rs12100717 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943687 | acaggcttgagccaA[C/T]GAACTCAGCTTGACA | 11169 |
rs12100725 | snp | A/C | 0.0584853 | 0.160693 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943790 | ATTAAAACAGTAAAC[A/C]GTCAAAAAATTAACC | 11169 |
rs12100729 | snp | A/G | 0.0810805 | 0.184299 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943661 | ccttggcctcccaaa[A/G]tgctaggattacagg | 11169 |
rs12147796 | snp | C/T | 0.438386 | 0.164349 | intron-variant | WDHD1 | GRCh38.p7 | 14:54941978 | ACTTTTGGCCAGGCA[C/T]GGTGGCTCATGTCTG | 11169 |
rs12323365 | snp | C/T | 0.0970103 | 0.197722 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996880 | cactgcaacctccgc[C/T]tcccgggttcaagcg | 11169 |
rs12432234 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | WDHD1 | GRCh38.p7 | 14:54985088 | Catttattcactcaa[C/G]acatatttacagaga | 11169 |
rs12434012 | snp | A/T | 0.11228 | 0.208646 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948153 | gggtgatttctgcac[A/T]tccaactgaggtacc | 11169 |
rs12434535 | snp | G/T | 0.125182 | 0.216612 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960972 | gcctggctaatattt[G/T]tattatttacttttt | 11169 |
rs12587037 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54963973 | attagctgggcgtgg[G/T]ggcatgcacctgcag | 11169 |
rs12588925 | snp | C/G | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982548 | TGTTTTCCACCTATT[C/G]TGCTTCCAACTCAGG | 11169 |
rs12588945 | snp | C/G | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982732 | TTAAAGCCTGAATGA[C/G]TAATAGAAAACACAT | 11169 |
rs12589254 | snp | G/T | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028590 | ACTATTCAGAGCTCA[G/T]CATAAGAAGAATCTG | 11169 |
rs12589476 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55009838 | ctttttttctttttt[G/T]gagacagagtctcac | 11169 |
rs12881591 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55005769 | AGTGCAGAAAGCCCT[C/T]ATGGGCTTTAGAATC | 11169 |
rs12881779 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55005850 | TTTTCTTTTTTTTTT[C/T]CTTAGAGCCTTCAGA | 11169 |
rs12887148 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54967464 | ACAAAATTTAAAAAG[G/T]TTTCAAAAGTTAGTA | 11169 |
rs12894439 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54972596 | aaaAAAAAAATGCCA[A/T]TGAGGCATATTCACT | 11169 |
rs12895097 | snp | A/T | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002298 | ATAAAAGCAAATTAG[A/T]TTTTAttgtttctgt | 11169 |
rs17128082 | snp | C/G | 0.0803491 | 0.183626 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940555 | TGCATTTGTATTAGT[C/G]TCTGCTTAGAAAACC | 11169 |
rs17128093 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957834 | TGTGAACCACCCCAA[C/T]GTGCCACTATGAAAC | 11169 |
rs17128105 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | WDHD1 | GRCh38.p7 | 14:54985158 | CAGCAATAAACAAAG[C/T]CACCACTCTTATTAA | 11169 |
rs17128116 | snp | A/G | 0.0460077 | 0.144524 | missense | WDHD1 | GRCh38.p7 | 14:54991322 | GATGTTACAAGTGGT[A/G]GATTGTGAATGCTGC | 11169 |
rs17128117 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997527 | AAATTAATAACTAAG[C/T]GCTATAAGAAGATAT | 11169 |
rs17128119 | snp | G/T | 0.0722614 | 0.17581 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000016 | ACAGCTATAAATGCA[G/T]GTATTAAGTCTGCAA | 11169 |
rs17128120 | snp | C/T | 0.485049 | 0.0851591 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007880 | TAACTGTTCCCTCTG[C/T]CAATCTGGAGAACAC | 11169 |
rs17253619 | snp | C/T | 0.120326 | 0.21374 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945026 | AGCAACCATGAACTC[C/T]GTACTTTCAACTTTT | 11169 |
rs17253633 | snp | C/T | 0.25045 | 0.25 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003199 | ATTATCACTTAAATC[C/T]AGAATGTACATTGTT | 11169 |
rs17832269 | snp | C/T | 0.387074 | 0.209071 | intron-variant | WDHD1 | GRCh38.p7 | 14:54965373 | TTCTAGACACCAAAC[C/T]TGGCCACTGGTCACA | 11169 |
rs17832281 | snp | C/T | 0.139903 | 0.224452 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988297 | AAAAATGTAGATTAA[C/T]AGTTGGCCAAGGCTC | 11169 |
rs28406393 | snp | C/T | 0.0872718 | 0.189788 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024883 | AGGAAAGCCAGGTAT[C/T]GTCCAAGGTTTCTCC | 11169 |
rs28406982 | snp | G/T | 0.095934 | 0.196885 | intron-variant | WDHD1 | GRCh38.p7 | 14:54980972 | AAAAATCAGCCAGGC[G/T]TGATGGTGCGCACCT | 11169 |
rs28407689 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55024749 | ATTAAGGGCGGTGCA[A/G]GATGTGCTTTGTTAA | 11169 |
rs28414866 | snp | C/T | 0.095934 | 0.196885 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013118 | ACAGTCCTAGCTGCC[C/T]GGGAGGCTGAACTGG | 11169 |
rs28420819 | snp | A/G | 0.0777841 | 0.181223 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028051 | GATATTCTTTCATTT[A/G]TACTTATCTTTGAGA | 11169 |
rs28422069 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55024690 | CCTTACCCCCAACCC[C/T]GTGCTCTCTGAAACG | 11169 |
rs28445630 | snp | A/G | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025320 | TCGAGAAACACCCAC[A/G]AATGATGAATAAATA | 11169 |
rs28446981 | snp | C/T | 0.443195 | 0.158668 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015228 | TGAGTCTACTAAAAA[C/T]ACAAACATTAGTCAG | 11169 |
rs28463462 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55024996 | TAAAAGAGGAAGGAA[C/T]GCCTCTTGCAGTTGA | 11169 |
rs28465254 | snp | A/G | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025202 | ATCTAAAAGCACAGC[A/G]CTTAATCCTTTACAT | 11169 |
rs28481699 | snp | A/T | 0.480697 | 0.0963277 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939831 | AGGTTGGCACAAAAG[A/T]AATCGCGGTTTTTGC | 11169 |
rs28489712 | snp | A/C | 0.0744748 | 0.178019 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017068 | ATGGAAACAAAGTAA[A/C]TCTTCTGGAAGTTCA | 11169 |
rs28495713 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55024705 | CGTGCTCTCTGAAAC[A/G]TGTGCTGTGTCAACT | 11169 |
rs28504998 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55024843 | GGGACACAAAAACTG[C/T]GGAAGGCCGCAGGGA | 11169 |
rs28513529 | snp | C/T | 0.095934 | 0.196885 | intron-variant | WDHD1 | GRCh38.p7 | 14:54980466 | CATTTTATACATATG[C/T]CAGCAGCAGTACTTC | 11169 |
rs28526752 | snp | A/C | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025169 | TTGTAAAGCATTGAG[A/C]TGTTTATGTGTATGC | 11169 |
rs28552618 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55024611 | AAAGAAGTAGACATA[A/G]GAGACTCCATTTTGT | 11169 |
rs28595580 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55003681 | CAATTCTCCTGCCTC[A/T]GCCTCCCGAGCAGCT | 11169 |
rs28658441 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55024752 | AAGGGCGGTGCAAGA[C/T]GTGCTTTGTTAAACA | 11169 |
rs28678578 | snp | A/C | 0.143622 | 0.226238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960508 | TATTTACTTCTTCTT[A/C]TTATTATTTTAGATG | 11169 |
rs28693954 | snp | A/G | 0.441021 | 0.161279 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015201 | TGGAGCCTGACCAAC[A/G]TGGCAAAACCCTGAG | 11169 |
rs28706216 | snp | A/T | 0.081446 | 0.184634 | intron-variant | WDHD1 | GRCh38.p7 | 14:54980538 | AGTCCAGGACCAGGT[A/T]CGGTGGCTCATGCCT | 11169 |
rs28719471 | snp | C/T | 0.081446 | 0.184634 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004188 | GATGGTCCTCAAAGA[C/T]TCCCACTCCACTTCC | 11169 |
rs28719727 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024704 | CCGTGCTCTCTGAAA[C/T]GTGTGCTGTGTCAAC | 11169 |
rs33937330 | in-del | -/TTCT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54995382 | TATTATTTCCTTCCA[-/TTCT]TTTGCTTGGGGTTTA | 11169 |
rs34029391 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55001520 | TCCTGCCTCAGCCTC[-/T]TCAAAGTGCTGGGAT | 11169 |
rs34071862 | in-del | -/A/TA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54966164 | AACCCCATCTCTACT[-/A/TA]AAAAAAAAAAAAAAA | 11169 |
rs34116293 | in-del | -/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55004603 | GATTACAGGCATGTG[-/C]CACCATGCCCAGCTA | 11169 |
rs34281869 | in-del | -/A | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963822 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 11169 |
rs34426307 | in-del | -/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55001142 | ATCCCTGTTCTATAT[-/C]TATTTCTAATTATAT | 11169 |
rs34476773 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54975725 | TTTAAAGAGACGGGG[-/T]TTTTGCTGTTGCCCA | 11169 |
rs34543433 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | WDHD1 | GRCh38.p7 | 14:54980012 | TTCACAGAGAATGTA[C/T]CAGCCATATCATATG | 11169 |
rs34581857 | in-del | -/A | 0.195837 | 0.244062 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954114 | AGCTTAAAAGTATTT[-/A]AAAAAAAAAAAAAGA | 11169 |
rs34651093 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010837 | TCAGAAGGCACGGCC[A/C]CAATGGCCACTGCCC | 11169 |
rs34660987 | in-del | -/TTGT | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011649 | TATTCGTGTGTGTGT[-/TTGT]GTGTATATATATATG | 11169 |
rs34670443 | in-del | -/TTCT | 0.483636 | 0.0889627 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995381 | GTATTATTTCCTTCC[-/TTCT]ATTTGCTTGGGGTTT | 11169 |
rs34783095 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54989663 | TTTAAGAAAACATAA[-/T]TTTTTTTTTTTTTTT | 11169 |
rs34843510 | in-del | -/AA | 0.482757 | 0.0912364 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996731 | TTTATAGTTTGGTAT[-/AA]AAGTCTAATGAGAAC | 11169 |
rs34857828 | snp | A/T | 0.0126979 | 0.078662 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940852 | AGAAATATATCCATT[A/T]CGTGGAAAGATAATA | 11169 |
rs34874701 | in-del | -/G | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963198 | AAGGGGGGGGGGGGG[-/G]AGATCAAATAACATC | 11169 |
rs34914902 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974509 | TTTTTTTTTTTTTTG[G/T]TATATTAAAGAAAGA | 11169 |
rs34949114 | in-del | -/C | | | frameshift-variant, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000889 | CTAAATCATACCTTT[-/C]CCATGCAGTCTTTGG | 11169 |
rs34988865 | snp | C/T | 0.40263 | 0.198 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008131 | TAGGTAAAAATGCAA[C/T]TAGTCTTCAACGTAT | 11169 |
rs35018704 | in-del | -/C | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026355 | AGGGAAATAGCATCA[-/C]TAAAGGCATGGAAGG | 11169 |
rs35102727 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55015699 | TTTGTTCCAATGGAA[-/T]TTTTTTTTTTTTTTT | 11169 |
rs35210143 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54961433 | CAGCACCACTTTCTC[-/T]TTTGCTCTCTGAGCT | 11169 |
rs35296144 | in-del | -/C | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55027852 | TCTATTCAGATCCCA[-/C]CTAAAGTTTACTGAA | 11169 |
rs35349292 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55007385 | ACATGTCTAATTGGT[-/A]AAAAAAGAAAATTTC | 11169 |
rs35354246 | in-del | -/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958128 | TCCTCCATCCAGCCA[-/T]TTTTTTTTTTTTTTT | 11169 |
rs35486238 | in-del | -/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54981239 | ATATTTATTGTTATT[-/G]TTATTAAAATAAAAG | 11169 |
rs35496040 | in-del | -/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54965998 | TGCAAGACCAACTAG[-/C]AAGATAGAACTTTAC | 11169 |
rs35628333 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54965010 | TAAGGCCATGTTGCA[-/T]TAAAGGTGACAGTAG | 11169 |
rs35695892 | in-del | -/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54984211 | CATGAAGAGAGCTCT[-/C]TAGCCGGGTGCAGTG | 11169 |
rs35744003 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54976558 | CAACAGCAGGCTACT[-/A]AAAAAGTGATTGCAG | 11169 |
rs35786669 | in-del | -/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54996662 | ATACACTGCAAAGAT[-/C]CCCAAGTTACTCCTA | 11169 |
rs35817115 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54988765 | AGCACTTAACAATGT[-/A]AAAAAAAAATCCCAT | 11169 |
rs35822700 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54976846 | AGCCAGGAAAATATG[-/A]AAAATATGAAAACAG | 11169 |
rs35839785 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953656 | TAAATCATGCTGCTA[C/T]AAAAACACATGCACA | 11169 |
rs35856470 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54993766 | TTTTTTGTTTTTCAT[-/A]AAAAAGTACTATTCA | 11169 |
rs35884834 | multinucleotide-polymorphism | AA/GC | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54999450 | GCCCCACTTCTAGAA[AA/GC]ACCTAGTGCTACCAA | 11169 |
rs35916951 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55003114 | TAAAAACTTTATTTT[-/A]AAAAAATTTTTAAAT | 11169 |
rs41309252 | snp | C/T | 0.0562307 | 0.157967 | missense | WDHD1 | GRCh38.p7 | 14:54941576 | ACAAATTCAGGTTCT[C/T]TTTTGCTTTTTCTTC | 11169 |
rs45459500 | snp | A/G | 0.249603 | 0.25 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007472 | TCTTCAAATCAATAT[A/G]TATCTCAGAAAAATG | 11169 |
rs45477791 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940030 | TATTCAGAATCAAAC[C/T]TAATGACAAAGCAAG | 11169 |
rs55692209 | snp | C/T | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011069 | CAGACTTCTTGCCTT[C/T]TGAACTGTGAGATAA | 11169 |
rs55704705 | snp | A/G | 0.267091 | 0.249415 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994622 | AAAAATTAGCCAGGC[A/G]TGGTGGCGCATGCCT | 11169 |
rs55802024 | snp | G/T | 0.47726 | 0.104176 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974495 | CCTGTTTTGTTTTGT[G/T]TTTTTTTTTTTTGTT | 11169 |
rs55965693 | snp | A/C | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972277 | GAGACTCGGTCTCAC[A/C]AAAAAAAAAAAAAAA | 11169 |
rs56188649 | snp | A/G | 0.249886 | 0.25 | intron-variant | WDHD1 | GRCh38.p7 | 14:54992184 | AATCGCTTGAACCCG[A/G]GAGACTCCGTCTCAA | 11169 |
rs56206440 | snp | C/T | 0.453209 | 0.145623 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984168 | GAAAAATATATTTCC[C/T]TCTTTATAAGTTTTC | 11169 |
rs56282786 | snp | C/G | 0.279991 | 0.248195 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020778 | AAACTTTACTAACAG[C/G]CTACTGTTGAGTAGA | 11169 |
rs56298796 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005901 | GCAGGGTTTTGCTTT[A/G]TTGCCTAGGCTGGAG | 11169 |
rs56328130 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | WDHD1 | GRCh38.p7 | 14:54986790 | GGAGGAAAAAGGAGG[C/T]AGCAGCTTTTAAAAA | 11169 |
rs56335168 | snp | A/C | 0.369754 | 0.219451 | intron-variant | WDHD1 | GRCh38.p7 | 14:54978414 | ATGGTGAGACCCCAT[A/C]TTTACAAAATATTTT | 11169 |
rs56681008 | in-del | -/CC/GCCCGACACC | 0.0414363 | 0.137845 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024955 | CCTGACCGTCCCGTA[-/CC/GCCCGACACC]AAGGGTCTGTGCTGA | 11169 |
rs56956725 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | WDHD1 | GRCh38.p7 | 14:54970014 | TCCTTTCATAATAAA[A/G]ACCTCCAACATACTA | 11169 |
rs57100945 | in-del | -/TATA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54987452 | ATATATATATATATA[-/TATA]AGCAATCATGATATT | 11169 |
rs57307089 | in-del | -/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55024954 | ACCTGACCGTCCCGT[-/C]AAAGGGTCTGTGCTG | 11169 |
rs57378772 | in-del | -/CA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55017754 | AAGATAACACACCAA[-/CA]AAAAAGAAGCCATAC | 11169 |
rs57622454 | snp | C/T | 0.300673 | 0.244811 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943105 | CTGTGCTGCGCCCTG[C/T]CATTCCTGGGGAAGT | 11169 |
rs57667631 | snp | A/G | 0.369346 | 0.219673 | intron-variant | WDHD1 | GRCh38.p7 | 14:54976349 | ACCTCAGCCTCCCGA[A/G]CAGCTGGGACTACAG | 11169 |
rs57800626 | in-del | -/AA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55016307 | TAATGAGCTAAAAAA[-/AA]GTATATCAAGTACAT | 11169 |
rs57922954 | snp | C/T | 0.369142 | 0.219784 | intron-variant | WDHD1 | GRCh38.p7 | 14:54990323 | AGAACTCAGGCCAGG[C/T]GCGGTGGCTCACGCC | 11169 |
rs58055971 | snp | C/T | 0.369142 | 0.219784 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969606 | AAAAAAGCCCTGGAC[C/T]AGAAAAATCACAGCT | 11169 |
rs58133286 | in-del | -/CA/CAA | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966357 | CAACAACAACAACAA[-/CA/CAA]AAAAAAACTTAAGAA | 11169 |
rs58224977 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54989711 | GTCACCCAAGCTGGA[A/G]TGCAGTGGCATGATC | 11169 |
rs59074935 | snp | C/T | 0.265727 | 0.249505 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989362 | TCATCTATCTCTAAA[C/T]AGTTTCTGACAGGAG | 11169 |
rs59191914 | in-del | -/GAA | | | cds-indel, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939599 | TGGAAAAAAAAAAAA[-/GAA]CACTGGAAAAAAACA | 11169 |
rs59220564 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966251 | GCTGAGGCAGAATTG[C/T]GTGAACCCGGGAGGC | 11169 |
rs59323730 | snp | C/T | 0.433382 | 0.169915 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972357 | GTGAGGCAGGCAGAT[C/T]ACTTGAGGCCAGGAG | 11169 |
rs59498123 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55016745 | CATAGCTGCATGTGG[A/C]TAGTAGCTACTGTAT | 11169 |
rs59510400 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55004463 | ACCAATGTTTATTTT[C/T]TTTTTTTGAGATAGA | 11169 |
rs59565763 | snp | A/T | 1.85917e-05 | 0.00304885 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944517 | ACTTAAGACAGAGTT[A/T]AAAGTGCCTCATGAT | 11169 |
rs59645597 | snp | A/G | 0.0755793 | 0.179102 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021345 | TTGGCAGTAGTTAGG[A/G]AGAACTCATTTCTAT | 11169 |
rs60028867 | snp | C/T | 0.372794 | 0.217765 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011638 | TAATTTTGTTATATT[C/T]GTGTGTGTGTTTGTG | 11169 |
rs60279550 | snp | A/C/T | 0.0715223 | 0.175059 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024954 | GACCTGACCGTCCCG[A/C/T]AAAGGGTCTGTGCTG | 11169 |
rs60283610 | in-del | -/CA | 0.493477 | 0.0567349 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981201 | AATTGAATATATATT[-/CA]GTTTTATTTTCACTT | 11169 |
rs60475452 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013178 | CCGGTCTGAGCAACA[C/T]GGCAAGATCCCGTTT | 11169 |
rs60594072 | in-del | -/T | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958143 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCGC | 11169 |
rs60609405 | in-del | -/A | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015405 | AAAAAAAAAAAAAAA[-/A]GGCTAGGGTGGGTTT | 11169 |
rs60615259 | in-del | -/AA | 0 | 0 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011550 | AAAAAAAAAAAAAAA[-/AA]GTATCCTGAGCAGAG | 11169 |
rs60642784 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54965583 | GCCCGTTAAAACATA[A/G]ACTGATGGGCAAAAG | 11169 |
rs60660567 | snp | C/T | 0.029116 | 0.117091 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994915 | CACCTCTCTTTCATT[C/T]TCTATGTTAGTAATT | 11169 |
rs60896254 | in-del | -/CT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54954724 | TAGTATAAAGAAGTT[-/CT]TTTTGTTTTTTTGGT | 11169 |
rs61379101 | in-del | -/G | 0.47726 | 0.104176 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974493 | AACCTGTTTTGTTTT[-/G]TTTTTTTTTTTTTTG | 11169 |
rs61514657 | in-del | -/CCAGCCC | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55024952 | AGACCTGACCGTCCC[-/CCAGCCC]GTAAAGGGTCTGTGC | 11169 |
rs61741224 | snp | C/G | 0.125054 | 0.216537 | missense | WDHD1 | GRCh38.p7 | 14:54981691 | AATCCACGTAACAAG[C/G]GGTACCTAAACACCA | 11169 |
rs61744409 | snp | A/G | 0.0675995 | 0.170968 | synonymous-codon, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:54995670 | TGAAGCCATCATGAG[A/G]TCTTCATCATCCTCA | 11169 |
rs61744418 | snp | C/T | 0.018437 | 0.0942262 | missense | WDHD1 | GRCh38.p7 | 14:54995638 | TCTAGGATGTGACTT[C/T]GCTGTCTAGGACGAC | 11169 |
rs61747434 | snp | A/G | 0.0186908 | 0.0948476 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54955599 | AGGACATATAGCTGG[A/G]GTTTCAGATAATACA | 11169 |
rs61975388 | snp | A/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987626 | ATTATTAAATACAAA[A/T]TCTTTTTTTTTGAAA | 11169 |
rs61975389 | snp | G/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989680 | TTTTTTTTTTTTTTG[G/T]AGACAGTTTTGCTCT | 11169 |
rs61975390 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55012013 | TAAAAAAAAAAAGTT[A/T]CTCACTTATGTATCC | 11169 |
rs61975391 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55015407 | AAAAAAAAAAAAAAG[A/G]CTAGGGTGGGTTTGG | 11169 |
rs61975392 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55015965 | CGGCCTCTCAAAGTG[C/T]TGGGATTATAGGCAT | 11169 |
rs61975393 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017719 | GAATTACAATTCATG[A/T]TTCTATCCAAATGAG | 11169 |
rs61975394 | snp | G/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021423 | TTTTTTTTTTTTTTG[G/T]AGACAGAGTTTTGCT | 11169 |
rs61977045 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:54956525 | CCTCTGTAATCCCAA[C/T]TCCTCGGGAGGCTGA | 11169 |
rs61977046 | snp | A/G | 3.17516e-05 | 0.00398432 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963180 | CAAGAAAGCTAATCC[A/G]AAAAGGGGGGGGGGG | 11169 |
rs61977047 | snp | A/C/G | 0.00403428 | 0.0447652 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963185 | AAGCTAATCCAAAAA[A/C/G]GGGGGGGGGGGGGAG | 11169 |
rs62417656 | snp | A/G | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952248 | TTAGAAAACCCCGTC[A/G]TCTCAGCCCAAAATC | 11169 |
rs66769866 | snp | C/T | 0.398714 | 0.200958 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979435 | TGTTGGGATTACAGG[C/T]GTGAGCCACCTCGCC | 11169 |
rs66820631 | snp | A/T | 0.368938 | 0.219895 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998835 | AGGTTATTAAGATCA[A/T]GTAAATGCTATTCAT | 11169 |
rs66881784 | in-del | -/G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54993749 | ACTCTTCTCACTAAT[-/G/T]TTTTTTTGTTTTTCA | 11169 |
rs67395322 | snp | G/T | 0.40733 | 0.194287 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018432 | CTTGACTTGTGGGAA[G/T]AATATTTTGATAGAA | 11169 |
rs67571433 | snp | A/G | 0.403158 | 0.197592 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981264 | TAAAAGACAGTAATA[A/G]AAGGTGAAATGCCAT | 11169 |
rs67945588 | snp | A/T | 0.0402882 | 0.136092 | intron-variant | WDHD1 | GRCh38.p7 | 14:54986696 | ATGGAATTATTTTTT[A/T]AAAAAAGCACAGAGA | 11169 |
rs68065548 | snp | C/T | 0.3744 | 0.216852 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979835 | CTAGGAATTCTTTTG[C/T]GTATGTAAAGCAAAT | 11169 |
rs71131243 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54955896 | ATTCCATGTTTTCCT[-/T]TTTTTTTTTTTTTTT | 11169 |
rs71131244 | in-del | -/AAAAAA/T | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972590 | AAAAAAAAAAAAAAA[-/AAAAAA/T]TGCCAATGAGGCATA | 11169 |
rs71131245 | in-del | -/C | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993351 | CTTGAACTCCTGGCC[-/C]TCAAGCAATCCTCCT | 11169 |
rs71131246 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54997090 | CCACAGCGCCCAGCC[-/T]TTTTTTTTTTTTTTT | 11169 |
rs71410642 | in-del | -/AAAAAA | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972553 | AAGCAAGACTGTCAC[-/AAAAAA]AAAAAAAAAAAAAAA | 11169 |
rs71412660 | snp | C/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972409 | GTGGTGAAAACCCAT[C/T]TCTACTAAAAATACA | 11169 |
rs71412661 | snp | C/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972514 | ACCTGGGAAATTGCA[C/T]TACTGCACTCCAGCC | 11169 |
rs71412662 | snp | A/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007267 | AAAGAAAAGAAAAAT[A/T]AGAATCACTTACCTT | 11169 |
rs71412663 | snp | A/C | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017859 | TTCTGTTTTTGTTGC[A/C]CAGGCTGGAGTGCAG | 11169 |
rs71412664 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55029073 | AAAAATGTATTCTTG[G/T]TTTTGCTAGTATCAT | 11169 |
rs71434508 | snp | A/C | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952424 | AAAATACCTAGGAAT[A/C]CAACTTACAAGGGAT | 11169 |
rs71448421 | multinucleotide-polymorphism | CT/GG | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983393 | GTGAAAAAATTTAGG[CT/GG]GGGGGCGGTGGCTCA | 11169 |
rs71448422 | in-del | -/A | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013194 | GCAAGATCCCGTTTC[-/A]AAAAAAAAAAAAAAA | 11169 |
rs72715557 | snp | C/T | 0.0158469 | 0.0875917 | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938674 | GGAGGATCACCTCAG[C/T]CCAGGGAGGTCAAGG | 11169 |
rs72715566 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979258 | CTGGGCTCAAGTGAT[C/T]CTCCCCTCTTAGCCT | 11169 |
rs72715571 | snp | C/G | 0.060684 | 0.163277 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54991270 | AAATGGCTTTTGCCG[C/G]GGAGTTGGCATGGGT | 11169 |
rs72715573 | snp | C/T | 0.482609 | 0.0916147 | intron-variant | WDHD1 | GRCh38.p7 | 14:54992853 | AGGAGTTCAAGGTTA[C/T]AGTGAGGTGTGATGA | 11169 |
rs72715575 | snp | A/G | 0.266819 | 0.249434 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006144 | GCTGGGATTATAGGT[A/G]TGAGCCACCACACAT | 11169 |
rs73266034 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969670 | CTACTGAAAATATTC[C/T]AAAATACCAACTCCT | 11169 |
rs73266045 | snp | A/T | 0.140242 | 0.224618 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981957 | AGTTTCAGTGAAAAC[A/T]ATGCCACCTGCTGGA | 11169 |
rs73266050 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984131 | TTGATTTGTATCACC[A/T]CCTTGCTATTTAATA | 11169 |
rs73266060 | snp | C/T | 0.139903 | 0.224452 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991516 | GACACTGACATGCTA[C/T]TTGCCTCTTTCACTG | 11169 |
rs73266074 | snp | A/G | 0.138886 | 0.22395 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003380 | CCAGCCATTGTGGGC[A/G]CGTGCCTCTAGTCCC | 11169 |
rs74050267 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957785 | CAACAGATATCCTCT[G/T]TCCTACTTCTAAGCC | 11169 |
rs74050278 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004869 | GAGCAGTGGGGAGCC[A/G]CAGACCAGTCTTCTG | 11169 |
rs74333230 | snp | A/T | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950782 | TGTAAAAGAACAGAA[A/T]TTATAACAAACTGTC | 11169 |
rs74359159 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016238 | TAATTTTATTGATTG[C/T]TATGCTTTTGAAATT | 11169 |
rs74359309 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026689 | ATTTGCACCTAAAAC[A/G]TTGTTTCTCAAAGAA | 11169 |
rs74367340 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975068 | ACATCTAGTCGGTAC[A/T]ATAATAAATGCTAAT | 11169 |
rs74393039 | snp | C/G | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974358 | GAATAGCTTGAACCC[C/G]GGAGGTCAAGGTTGC | 11169 |
rs74584279 | snp | A/C | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54980323 | AGTGAGACTCTGTCT[A/C]AAAAAAAAAAAAGAC | 11169 |
rs74631108 | snp | A/G | 0.0872718 | 0.189788 | intron-variant | WDHD1 | GRCh38.p7 | 14:54973977 | CTGTTAAATATCCCC[A/G]TCATAGAAGAATTCA | 11169 |
rs74732888 | in-del | -/CAACCTTCT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54946303 | GCAACCCTTCTGACT[-/CAACCTTCT]GAGTGGCTAGGACTA | 11169 |
rs74735607 | snp | A/T | 0.0475351 | 0.146656 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943844 | GAGGTTGTCTCTATA[A/T]AAAAAAAAAAGAGGA | 11169 |
rs74776964 | snp | C/G | 0.0603597 | 0.1629 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943994 | ATTACATAATAATTA[C/G]TACATATCCATATTA | 11169 |
rs74784943 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54991821 | TTTCATACAACACTA[C/T]TTTTACTTAAAAAAC | 11169 |
rs74785625 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | WDHD1 | GRCh38.p7 | 14:54965012 | AAGGCCATGTTGCAT[A/G]AAGGTGACAGTAGTG | 11169 |
rs74897522 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999451 | CCCCACTTCTAGAAG[A/C]ACCTAGTGCTACCAA | 11169 |
rs74935067 | snp | A/G | 0.139564 | 0.224285 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940633 | AGTTAAATACTTTCC[A/G]TAACTTTGCTCTCTT | 11169 |
rs74991960 | snp | A/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988775 | AATGTAAAAAAAAAA[A/T]CCCATCTCTTGCATT | 11169 |
rs75021747 | snp | C/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955791 | AAACATCTATAATTA[C/T]TGAGAATTCTTATAC | 11169 |
rs75081088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004490 | TAGAGTCTCGCTCTA[C/T]CACCTGAGCTAGAGT | 11169 |
rs75106569 | snp | C/G | 0.0558544 | 0.157504 | intron-variant | WDHD1 | GRCh38.p7 | 14:54976279 | TCCTTCTGTCACGCA[C/G]GTTGGGGTGCAGGGG | 11169 |
rs75160766 | snp | A/G | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950872 | GGAGCAGGTTCTTCA[A/G]TTTCCATGTAGTTGA | 11169 |
rs75164364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957445 | GTAGAAAAGACAACT[C/T]TCAGCCCAAGTGCTG | 11169 |
rs75181519 | snp | A/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989662 | ATTTTAAGAAAACAT[A/T]ATTTTTTTTTTTTTT | 11169 |
rs75216894 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014996 | AAAATGAAGTCTAGG[C/T]CACCTATTTAGAATA | 11169 |
rs75249088 | in-del | -/AA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974103 | ATTTAAAAAAAAAAA[-/AA]CAATGAAAAACCTGG | 11169 |
rs75376959 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975862 | AAATTATTTTTCACA[A/G]AATGTACTTTCTTTT | 11169 |
rs75484067 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028416 | TTCTGAGTGACCTAA[A/T]TTTTTTTTTTTGGAG | 11169 |
rs75484710 | snp | A/T | 0.0433465 | 0.140692 | intron-variant | WDHD1 | GRCh38.p7 | 14:55010252 | ACTACCCTGAAACAA[A/T]TAAACAAGGCCTTTT | 11169 |
rs75643975 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958026 | ACTTTTCCCTATTTA[A/T]TGGCCCCTAAAGTCT | 11169 |
rs75652141 | snp | A/G | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998209 | GACTTTGCCTCAAAG[A/G]AAAAAAAAAATTTTT | 11169 |
rs75673309 | snp | A/G | 0.100231 | 0.200173 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975784 | GATCCTCCTGCCCCT[A/G]TCTTTTAAGTAGCTG | 11169 |
rs75789517 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966358 | CAACAACAACAACAA[A/C]AAAAAACTTAAGAAT | 11169 |
rs75790544 | snp | A/C | 0.137527 | 0.223271 | intron-variant | WDHD1 | GRCh38.p7 | 14:54978408 | GGCAAGATGGTGAGA[A/C]CCCATCTTTACAAAA | 11169 |
rs75794050 | snp | C/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950891 | TGTACCCAGTAGTCA[C/T]TCAGGAGCAGGTTGT | 11169 |
rs75811572 | snp | A/C | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966356 | AACAACAACAACAAC[A/C]AAAAAAAACTTAAGA | 11169 |
rs75836122 | snp | A/C | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964638 | AGCGAGACTTCGTTT[A/C]AAAAAAAAAAAAAGA | 11169 |
rs75882862 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028414 | CTTTCTGAGTGACCT[A/T]ATTTTTTTTTTTTGG | 11169 |
rs75905424 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | WDHD1 | GRCh38.p7 | 14:54978710 | CCACCAATTCCTCTG[C/T]AGTTCTCTACTAATT | 11169 |
rs75937340 | snp | A/C/T | 1.70845e-05 | 0.00292267 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008370 | ACTAGCTGATGCCTG[A/C/T]AGGAATAAACAATAC | 11169 |
rs75975302 | snp | A/G | 0.04875 | 0.148319 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016907 | TTTCAGATGAGATCA[A/G]GTGCGTTCAGGGTGG | 11169 |
rs76028221 | snp | A/G | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950854 | TCCATGTAGTTGAGC[A/G]GTTTTGGGTGAGTTT | 11169 |
rs76164691 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55023400 | TGTCTCAAATTTCCT[G/T]TTCACAGTGGTCCTT | 11169 |
rs76202473 | snp | C/T | 0.0558544 | 0.157504 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55012016 | AAAAAAAAAGTTTCT[C/T]ACTTATGTATCCAGC | 11169 |
rs76243320 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969358 | GAAAAAAAAAAAAAA[A/G]AGAGAGAGAGAAAGA | 11169 |
rs76512171 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55012010 | CTCTAAAAAAAAAAA[G/T]TTTCTCACTTATGTA | 11169 |
rs76557077 | snp | A/G | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003572 | ATATATGTATAAAAA[A/G]GAAAGAAAAACGAAC | 11169 |
rs76584809 | snp | A/C | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974105 | TTAAAAAAAAAAAAA[A/C]AATGAAAAACCTGGT | 11169 |
rs76632389 | snp | C/T | 0.0513262 | 0.151752 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028302 | AGGTTTGTATATGAA[C/T]GAAGAGGAAGAATGA | 11169 |
rs76633661 | snp | A/G | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54970635 | CCAAAAAAAAAAAAA[A/G]AGAAAGAAAGAAGAA | 11169 |
rs76645665 | snp | C/T | 0.277778 | 0.248452 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950834 | AACTAGAACTCAGGA[C/T]TAAGAAACTCACCCA | 11169 |
rs76659857 | snp | C/T | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950866 | AACCACTCAAATACA[C/T]GGAAACTGAACAACC | 11169 |
rs76664564 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54982747 | CTAATAGAAAACACA[G/T]TTAGAAATGGTTGAT | 11169 |
rs76717638 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54991819 | TTTTTCATACAACAC[A/T]ACTTTTACTTAAAAA | 11169 |
rs76771649 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54985447 | TCGAAGAACACAAAG[A/C]GGCAGTATGGCCAGA | 11169 |
rs76982558 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55012009 | GCTCTAAAAAAAAAA[A/G]GTTTCTCACTTATGT | 11169 |
rs77065866 | snp | A/C/T | 0.0803491 | 0.183626 | intron-variant | WDHD1 | GRCh38.p7 | 14:54980340 | AAAAAAAAAAAGACA[A/C/T]AATTCAGTGGTTTTT | 11169 |
rs77116074 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | WDHD1 | GRCh38.p7 | 14:54985209 | ACAAATTAAAAAACA[C/T]AAAAAGAACAAAAAA | 11169 |
rs77176256 | snp | G/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021420 | TCCTTTTTTTTTTTT[G/T]TGGAGACAGAGTTTT | 11169 |
rs77193434 | snp | G/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975365 | TAATTTTTTTTTTTT[G/T]GAGACAGAGTTTCCC | 11169 |
rs77234669 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | WDHD1 | GRCh38.p7 | 14:54990835 | TCTAATATATTATAC[C/T]AGTAGTTGCCTTCTA | 11169 |
rs77241359 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994335 | GTTATTCATAATATT[A/G]CCATTATGCCTTTGA | 11169 |
rs77333710 | snp | A/G | 0.0970103 | 0.197722 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997560 | AACCATTCCATTTAT[A/G]GTCCTAAAAGTTTGT | 11169 |
rs77356959 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954343 | ATCAAGAAAATAGGT[A/G]ACATACTGTGTTTGT | 11169 |
rs77425549 | snp | A/G | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004444 | TTTCCCTTTTTTTTT[A/G]GCAACCAATGTTTAT | 11169 |
rs77440023 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014410 | AAAATTATTTATTTG[C/T]AAGAATGTAAGAAAG | 11169 |
rs77561506 | snp | A/G | 0.0542238 | 0.155473 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957017 | CTTACTGCAGATGAG[A/G]GTAGCTGAAACAGTA | 11169 |
rs77655308 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974493 | AACCTGTTTTGTTTT[G/T]TTTTTTTTTTTTTTG | 11169 |
rs77662341 | snp | C/T | 0.021333 | 0.101051 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002252 | GAAGAAGGAAAAAGG[C/T]ACAAAATTCATTCAG | 11169 |
rs77678033 | snp | A/G | 0.198944 | 0.244731 | upstream-variant-2KB, utr-variant-5-prime | WDHD1, SOCS4 | GRCh38.p7 | 14:55027372 | ACGAGGTGCAGGAGT[A/G]GTTGGGCCTCCCCTC | 11169 |
rs77717191 | snp | G/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987637 | CAAATTCTTTTTTTT[G/T]GAAATGGAGTTTTGC | 11169 |
rs77808847 | snp | A/G | 0.0513262 | 0.151752 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028320 | AGAGGAAGAATGATT[A/G]GCTTAAAAACAACTT | 11169 |
rs77810789 | snp | A/G | 0.081446 | 0.184634 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983885 | ACATTTTATTTCATC[A/G]AAGATATCTCAAATA | 11169 |
rs77852019 | snp | C/G | 0.0569829 | 0.158885 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961290 | TGAGTTTGAGACCAG[C/G]CTGGACAACAGAGTG | 11169 |
rs77904869 | snp | G/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987638 | AAATTCTTTTTTTTT[G/T]AAATGGAGTTTTGCT | 11169 |
rs77911976 | snp | A/G | 0.198944 | 0.244731 | upstream-variant-2KB, utr-variant-5-prime | WDHD1, SOCS4 | GRCh38.p7 | 14:55027373 | CGAGGTGCAGGAGTG[A/G]TTGGGCCTCCCCTCT | 11169 |
rs77956891 | in-del | -/AA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54988749 | AGTAAAAAAAAAAAA[-/AA]GCACTTAACAATGTA | 11169 |
rs77973554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955286 | CCCCATTAAACTATT[C/T]AAAAACAAACAAAAA | 11169 |
rs78051477 | snp | A/G | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950871 | CTCAAGTACATGGAA[A/G]CTGAACAACCTGCTC | 11169 |
rs78079035 | snp | A/T | 0.0648419 | 0.167978 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974075 | CTATGTGCATAAACC[A/T]CCTGGAAGAGGAATT | 11169 |
rs78117497 | snp | G/T | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021421 | CCTTTTTTTTTTTTT[G/T]GGAGACAGAGTTTTG | 11169 |
rs78138184 | snp | A/C | 0.040671 | 0.13668 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969853 | GAAGTTAATACACCA[A/C]AACCAGTAGGTTTTA | 11169 |
rs78145109 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999450 | GCCCCACTTCTAGAA[A/G]CACCTAGTGCTACCA | 11169 |
rs78167854 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54991297 | GGGTCCATCATAAAA[C/T]GGCCTTTGGGATGTT | 11169 |
rs78202195 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020720 | ATTACAGGTTCCAAC[C/T]CCTAAACAGTCAAAA | 11169 |
rs78246942 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001742 | GTAAATATCTACGCA[C/T]GTAAGAGACAGAGAA | 11169 |
rs78273278 | in-del | -/CTA | 0.264906 | 0.249555 | intron-variant | WDHD1 | GRCh38.p7 | 14:54973266 | GATACTAAGTAGAAG[-/CTA]GACCCTAGGGTTTAA | 11169 |
rs78292854 | snp | G/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954737 | TTCTTTTTGTTTTTT[G/T]GGTTTTTTTGAGACA | 11169 |
rs78296321 | snp | G/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989678 | ATTTTTTTTTTTTTT[G/T]GGAGACAGTTTTGCT | 11169 |
rs78301003 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54991820 | TTTTCATACAACACT[A/G]CTTTTACTTAAAAAA | 11169 |
rs78318278 | snp | C/T | 0.0163158 | 0.0888352 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007421 | TTTATGAAAATCCCC[C/T]CCAAAATATATGCAG | 11169 |
rs78320232 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984958 | TTTGTGGTAAATTAC[C/T]AGACTGACTAGCACT | 11169 |
rs78357054 | snp | A/G | 0.030278 | 0.119257 | upstream-variant-2KB, utr-variant-5-prime | WDHD1, SOCS4 | GRCh38.p7 | 14:55027153 | GACAGAGGTCGCCGG[A/G]TGGTGGCGTCAGCTG | 11169 |
rs78379848 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950857 | GTTTCCATGTAGTTG[A/T]GCGGTTTTGGGTGAG | 11169 |
rs78385171 | snp | C/G | 0.277778 | 0.248452 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950893 | AACCTGCTCCTGAAT[C/G]ACTACCGGGTACATA | 11169 |
rs78420354 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | WDHD1 | GRCh38.p7 | 14:54941808 | CAGAATAATTAGCAC[C/T]TGAATTAAGTGTTCT | 11169 |
rs78426644 | snp | C/T | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950865 | GTTGTTCAGTTTCCA[C/T]GTAGTTGTGCAGTTT | 11169 |
rs78504180 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017711 | TGAATTTGGAATTAC[A/C]ATTCATGATTCTATC | 11169 |
rs78507472 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55023215 | ACCTACCTTTCACTT[G/T]AAGTTGTCAGATAAT | 11169 |
rs78587067 | snp | A/G | 0.277778 | 0.248452 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950900 | TCCTGAATGACTACT[A/G]GGTGCATAACGAAAT | 11169 |
rs78722135 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939159 | TCAAGATGAAAACTT[A/G]GGGGAAAATTATATA | 11169 |
rs78766290 | snp | A/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988774 | CAATGTAAAAAAAAA[A/T]TCCCATCTCTTGCAT | 11169 |
rs78788859 | snp | C/G | 0.0596104 | 0.162024 | intron-variant | WDHD1 | GRCh38.p7 | 14:54976590 | ATTTTATTCCCCGAA[C/G]TTCCATGTACCGCTA | 11169 |
rs78794799 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | WDHD1 | GRCh38.p7 | 14:55023552 | AGTATGTCCAGCATC[A/C]CTAGTGGCACTTCAT | 11169 |
rs78884146 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | WDHD1 | GRCh38.p7 | 14:54985732 | GTCCAAGAGATGACA[C/T]CCAGGTTGTATTAGC | 11169 |
rs78929890 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | WDHD1 | GRCh38.p7 | 14:54968034 | CCATTAATACCTGTC[A/G]TGGAATCCATGTTAT | 11169 |
rs78936008 | snp | C/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969585 | AAATAAAAAACCTAT[C/T]AACCAAAAAAAGCCC | 11169 |
rs79037730 | snp | A/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969584 | TAAATAAAAAACCTA[A/T]CAACCAAAAAAAGCC | 11169 |
rs79058386 | snp | A/G | 1.91481e-05 | 0.00309414 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955741 | ATCTAGTATAATTTT[A/G]TATGTTTTATAAGCA | 11169 |
rs79077061 | snp | A/T | 0.164219 | 0.234823 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024488 | ATATTTCCTGAATGT[A/T]TACTCTTTTCTACAC | 11169 |
rs79141206 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54995381 | TGTATTATTTCCTTC[C/T]ATTTGCTTGGGGTTT | 11169 |
rs79201207 | snp | C/G | 0.0718919 | 0.175435 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000035 | TTAAGTCTGCAATCT[C/G]TAACCAGAAGTCTAA | 11169 |
rs79229660 | snp | A/G | 0.0162398 | 0.0886349 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028958 | GTAATTGTTATTAAT[A/G]TCTCATGTTACTAAA | 11169 |
rs79245615 | snp | C/G | 0.139564 | 0.224285 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939431 | GTAAAGTAACCTCCT[C/G]TGAGGAGTTTTTGCT | 11169 |
rs79253091 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957828 | ATTAAATGTGAACCA[A/C]CCCAACGTGCCACTA | 11169 |
rs79281058 | snp | A/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989664 | TTTAAGAAAACATAA[A/T]TTTTTTTTTTTTTTG | 11169 |
rs79339059 | snp | A/G | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983809 | TAGGCATGAGCCACC[A/G]TGCCCAGCCAAAAAA | 11169 |
rs79377719 | snp | G/T | 0.0607341 | 0.163335 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958776 | CCTGATGCTCAAATG[G/T]TGGAGATTCCCTAGG | 11169 |
rs79469913 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | WDHD1 | GRCh38.p7 | 14:54973557 | CACAGTATGAGGTGG[C/T]AGTGTGAATACCTCA | 11169 |
rs79590152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950910 | CTACTAGGTGCATAA[C/T]GAAATGAAGGCAGAA | 11169 |
rs79658987 | snp | A/G | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977924 | GTGGAAAAAAAAAAA[A/G]AGCATGTTAAGAAAA | 11169 |
rs79754851 | snp | A/T | 0.139564 | 0.224285 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54938990 | AGGGTACATGCTGGG[A/T]ACTGAGGGATGAAGT | 11169 |
rs79758944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018463 | CTCCTATTTTTAATT[A/G]TATTAATTTATGTTC | 11169 |
rs79920918 | snp | A/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004443 | CTTTCCCTTTTTTTT[A/T]AGCAACCAATGTTTA | 11169 |
rs79968281 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55002618 | ATGATTACTTTTTTT[C/T]CCCCCAAGAGACAGT | 11169 |
rs80028742 | snp | A/G | 0.375 | 0.216506 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950805 | TCTGATTGCACTGTG[A/G]TCTGAGAGAGAGTTT | 11169 |
rs80066034 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | WDHD1 | GRCh38.p7 | 14:55023371 | CATGCCTGCTGGCAT[A/G]GCTGCAGTAACAGTG | 11169 |
rs80067373 | snp | A/G | 0.081446 | 0.184634 | intron-variant | WDHD1 | GRCh38.p7 | 14:54976005 | GAAATTCTGTGAAAT[A/G]GGTACACTGTGGTTT | 11169 |
rs80092899 | snp | A/C | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974433 | GAGAGATTCTGTCTC[A/C]AAAAAAAAAAAAATT | 11169 |
rs80274382 | snp | G/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979503 | CATATTCTACTTTCA[G/T]TTCTTTACCTCCCAT | 11169 |
rs80344912 | snp | C/T | 0.00676609 | 0.0577691 | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938914 | TGTAATAATATCATC[C/T]GTTAAATTTCTTTGG | 11169 |
rs80351669 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009309 | CTACAACCATTTTTA[A/G]AAGTACTATACCTTT | 11169 |
rs111226731 | snp | C/G | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979010 | TTTCATTGGCTCCTT[C/G]TTTTAAATTATCAAT | 11169 |
rs111234999 | snp | A/G | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958424 | GAGCCACCACGCCCG[A/G]TCATCCAGCCAAATT | 11169 |
rs111242749 | snp | A/G | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017558 | ATGTTGGCCAGCCTG[A/G]TCTCGAACTCTTGAC | 11169 |
rs111243557 | snp | C/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949114 | CCCCCCCCAAAGGAA[C/T]GCAGCTCCTCACCAG | 11169 |
rs111247838 | snp | A/G | 0.0777841 | 0.181223 | intron-variant | WDHD1 | GRCh38.p7 | 14:54985565 | GCTATCAGAAGTTTG[A/G]CTTTGATTCTAAAAG | 11169 |
rs111261144 | snp | C/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013901 | AACAGAGCAAGACTC[C/T]ATCTCAAGGAAAAAA | 11169 |
rs111394414 | snp | A/G | 0.139564 | 0.224285 | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938573 | AGCCTGGGCAACATG[A/G]TGAAACCCATCTATG | 11169 |
rs111401015 | snp | A/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943209 | TTCACATGGCAGAAG[A/T]TTATCAGAAGCAAGC | 11169 |
rs111421531 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013893 | GCCTGGGCAACAGAG[A/C]AAGACTCTATCTCAA | 11169 |
rs111478437 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993009 | GTGTCAGTATAAAGA[A/G]GATCTATAAACTTCA | 11169 |
rs111483506 | snp | C/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960185 | GTTTATTTATTTATT[C/T]GAGATGGAGTCTCGC | 11169 |
rs111511584 | snp | C/T | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016386 | TAATGAAAATATAAC[C/T]TGAATAAAATGTTTG | 11169 |
rs111535456 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | WDHD1 | GRCh38.p7 | 14:54990898 | AGTATAATCTTCTAT[C/G]TAACAATGACCATGA | 11169 |
rs111552243 | snp | C/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974732 | CTTGGGAGGCTGAGG[C/T]ATAAGAATCACTTGA | 11169 |
rs111558457 | snp | A/G | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004489 | ATAGAGTCTCGCTCT[A/G]TCACCTGAGCTAGAG | 11169 |
rs111770978 | snp | A/G | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998886 | AGCCAACACTTATAA[A/G]GTATGCCAAACTTAT | 11169 |
rs111772574 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991872 | TTATGCAGAATTGGA[A/T]CTTTGGCAAACATTT | 11169 |
rs111773217 | snp | C/T | | | missense | WDHD1 | GRCh38.p7 | 14:54962785 | TCAGCTTCTCCACTG[C/T]CCTCAGCATCTTCTT | 11169 |
rs111781973 | snp | C/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008303 | AACTTTAAATTTAAA[C/T]TGCTGAGTTTACCTG | 11169 |
rs111812968 | snp | C/G | 0.00323367 | 0.0400796 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989245 | TAAATATAAGTCTGA[C/G]AAAAACTGAAGCTCC | 11169 |
rs111816263 | snp | A/G | 1.72258e-05 | 0.00293472 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013440 | AAGCATAAAAATCAC[A/G]TGCCAGTATCATTTC | 11169 |
rs111824685 | snp | A/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007638 | ATAATCATACACACA[A/T]ACACAAAACCCCAAT | 11169 |
rs111860454 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017506 | CACCACCCACACCTG[A/G]CTAAATTTCGTATTT | 11169 |
rs111864461 | snp | C/T | 0.14933 | 0.228835 | intron-variant | WDHD1 | GRCh38.p7 | 14:55010007 | TTGTATTAGTAGAGA[C/T]GGGGTTTTGCCATGT | 11169 |
rs111864525 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54982133 | TGCCTCAGCCTCCCG[A/G]GTAGCTGGGACTACA | 11169 |
rs111893223 | snp | A/G | 0.249038 | 0.249998 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983491 | CAGCCTGGCCAGCAT[A/G]GTAAAACCCTGTCTC | 11169 |
rs111913176 | snp | C/T | 0.0138799 | 0.0821421 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940733 | ACATGATGCCTTGGA[C/T]TGCAATACTGTCACA | 11169 |
rs111931746 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939599 | TGGAAAAAAAAAAAA[A/G]AACACTGGAAAAAAA | 11169 |
rs111982318 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981842 | ATCTAAGATTATTAC[A/G]TAAAATTTCATTAAC | 11169 |
rs112011978 | snp | C/G | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944936 | AACTGCCTGGAGACT[C/G]CAGGATCAATGAACT | 11169 |
rs112017165 | snp | C/T | 0.0729998 | 0.176553 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969272 | ACCTTGTGATCCGCC[C/T]GCCTATGCCTCCCAA | 11169 |
rs112027560 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948728 | TGGGTCCATGATCCA[C/G]AAGTAGCCTAACTGG | 11169 |
rs112028956 | snp | A/G | 0.5 | 0 | missense | WDHD1 | GRCh38.p7 | 14:54966488 | ACCGCAAGCATTTTC[A/G]TTAAAAGTTCCTGTT | 11169 |
rs112030294 | snp | A/G | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987907 | GCCGGGATTACAGGC[A/G]TGAGCCACCATGCCC | 11169 |
rs112035792 | snp | C/T | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019386 | TCAAATTTTCAAAAC[C/T]ATTGGCATAAGGGTG | 11169 |
rs112045621 | snp | A/G | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004484 | TTGAGATAGAGTCTC[A/G]CTCTATCACCTGAGC | 11169 |
rs112071910 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54966165 | AACCCCATCTCTACT[A/T]AAAAAAAAAAAAAAA | 11169 |
rs112075250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988238 | TGTTTTTCCGTTTTT[C/T]TTTCCTTTCTCGAAG | 11169 |
rs112076739 | snp | C/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974049 | TTGATGACGACGGAG[C/T]TTCCTGGAAACTATG | 11169 |
rs112077106 | in-del | -/A | 0.0158469 | 0.0875917 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001660 | ACAATCAAGATGAAG[-/A]AAACTAGTAAGTGAA | 11169 |
rs112110871 | snp | A/G | 0 | 0 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55027878 | CTGAAGTGAATATTT[A/G]TAACCAAAAGAAGAG | 11169 |
rs112123124 | snp | A/G | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977686 | CTAAATAAATAAATA[A/G]AAAGGGCTCTTATAT | 11169 |
rs112227923 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | WDHD1 | GRCh38.p7 | 14:54956310 | GGGGTCTGAGTATAT[A/G]TATTTTTAAAAAGTG | 11169 |
rs112234406 | snp | C/G | 0.136166 | 0.22258 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961971 | CCTCCCGAGTAGCTG[C/G]GATTACAGGCACATA | 11169 |
rs112297457 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991066 | GCTAACCATAAAATA[A/T]ACCAACCACAAAACT | 11169 |
rs112304372 | snp | C/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974044 | GGGTTTTGATGACGA[C/T]GGAGTTTCCTGGAAA | 11169 |
rs112318245 | snp | C/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954273 | CCTGGGCAACAAGAG[C/T]GAAACTCCGTCTCAG | 11169 |
rs112344843 | snp | C/T | 0.5 | 0 | missense, intron-variant | WDHD1 | GRCh38.p7 | 14:54995804 | AATCCTTTTCCACTC[C/T]GCTAGATACCTTGAA | 11169 |
rs112393098 | in-del | -/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975703 | GACTTAAATTAATGC[-/T]TTTTTTTTTTAAAGA | 11169 |
rs112477354 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54946764 | AAGTGTTAGGCTTGG[C/G]CAGGTGTGGTGGCTC | 11169 |
rs112491513 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54946763 | AAAGTGTTAGGCTTG[C/G]CCAGGTGTGGTGGCT | 11169 |
rs112519613 | snp | C/T | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022744 | CTTTCTCCTCAATGA[C/T]TTTCGTAATGGTGTC | 11169 |
rs112522682 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967840 | TGCCCAGGCTGGACT[C/T]GAACTCCTGGGCTAA | 11169 |
rs112522777 | snp | A/G | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008302 | AAACTTTAAATTTAA[A/G]TTGCTGAGTTTACCT | 11169 |
rs112551338 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969258 | GTCTCGATCTCCTGA[C/T]CTTGTGATCCGCCCG | 11169 |
rs112595648 | snp | C/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971924 | GGGAACGGTGGGTCA[C/T]ACCCATAATCCCAGA | 11169 |
rs112602642 | snp | A/G | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54978874 | ATTTGTTACCTTTTG[A/G]CTACCAAATCTATCT | 11169 |
rs112623682 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945689 | GGGACTACAGGTACG[C/T]GCCACCACACCCAGC | 11169 |
rs112636335 | snp | A/G | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54970664 | AAAGAAAAAGACCAT[A/G]CTCCCCAAAGCAATC | 11169 |
rs112646166 | snp | C/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955486 | TAAGGAATAACAGCA[C/T]TGCATAATTTTGTAT | 11169 |
rs112651988 | snp | A/G | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997749 | AACCCCGTCTCTACT[A/G]AAAATGCAAAAATTA | 11169 |
rs112653363 | snp | A/C | 0.0670745 | 0.170406 | intron-variant | WDHD1 | GRCh38.p7 | 14:54990395 | GAGGTCAGGAGATCG[A/C]GACCATCCTGTCTAA | 11169 |
rs112710499 | snp | G/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995444 | AGCTTGGATTATAGA[G/T]TTGAAACCTTTTTTA | 11169 |
rs112728495 | in-del | -/A | 0.481473 | 0.0944461 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998209 | GACTTTGCCTCAAAG[-/A]AAAAAAAAAATTTTT | 11169 |
rs112754983 | in-del | -/A | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964638 | GCGAGACTTCGTTTC[-/A]AAAAAAAAAAAAAGA | 11169 |
rs112758038 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54952367 | ACAAACAGAGAGCCA[A/T]ATCATGAGTGAACTC | 11169 |
rs112760614 | snp | C/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015124 | GTCCAACTGGCCTGG[C/T]ATTGTCCAGGAATTT | 11169 |
rs112793030 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55027565 | AAACAATATCCGGAT[A/C]CCTAAAAGGATCCGG | 11169 |
rs112868924 | snp | C/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979967 | TCCTTTTTAACAGCT[C/T]TGTCAAGATATGATT | 11169 |
rs112879674 | snp | A/G | 0.491987 | 0.0627894 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953555 | caaccattgtggaag[A/G]cggtgtggcgattcc | 11169 |
rs112884718 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967576 | TAGGCATAAAGACTA[C/T]CCCTACATGCATTTC | 11169 |
rs112893906 | snp | A/C/T | 0.0138799 | 0.0821421 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963364 | ACAATTAATGGTGGG[A/C/T]CAGTTTGGCAGCATT | 11169 |
rs112927738 | snp | A/G | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996824 | ACAGAGTGGAGTCTC[A/G]CTCTGTCGCCAGGCT | 11169 |
rs112944183 | snp | C/T | 0.0581099 | 0.160244 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026272 | AACCGTAGGAAAATA[C/T]TATAGTTTAGGAATC | 11169 |
rs112949728 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942832 | TAAATGTTTAGGGTT[C/T]ACCTTAAAAATACTG | 11169 |
rs112954483 | snp | C/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966921 | TAACTAACTGCAAGA[C/T]TTCAAATGACTTTTG | 11169 |
rs112991712 | snp | C/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972450 | GGGTGTGGTGGTGAA[C/T]GCCTGTAATCCCAGC | 11169 |
rs113001206 | snp | C/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998419 | ACAGCCGTGAGCCAC[C/T]GTGCCCAGCCAAAAT | 11169 |
rs113018753 | snp | C/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003776 | ATCATGTTGGCCAGG[C/T]TGGTCTCGAACTCCT | 11169 |
rs113041954 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998128 | TGAGGCAGGAGAATC[A/G]CTTCAACCCAGGAGG | 11169 |
rs113066369 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969557 | ATAATGAGTTCCAAA[A/C]TTGAATCGTAATAAA | 11169 |
rs113103048 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975534 | TGTATTTTTAGTAGA[A/G]ACAGGGTTTCACCAT | 11169 |
rs113144063 | snp | G/T | 0.067446 | 0.170804 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975029 | TTCCAGGCCACAGCC[G/T]CATTTATCTTTGTGT | 11169 |
rs113168315 | snp | A/C | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54968658 | AGCTCCATATAAGCA[A/C]AATCAGAAAATGGCA | 11169 |
rs113186686 | snp | A/G | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989989 | AAATTGATACCACTT[A/G]GAAAACTTATCTTCC | 11169 |
rs113210313 | snp | A/G | 0.5 | 0 | synonymous-codon, intron-variant | WDHD1 | GRCh38.p7 | 14:54995748 | GTCATTTAGAAAATC[A/G]CCAGCATTACTCATA | 11169 |
rs113259096 | snp | C/G | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947727 | CTCCCAAGTAGCTGG[C/G]ATTACAGGCATGAGC | 11169 |
rs113326119 | snp | A/G | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015670 | CCAATGGTGATGAGA[A/G]AAGTATTTCACGTTT | 11169 |
rs113397363 | snp | G/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008135 | TAAAAATGCAATTAG[G/T]CTTCAACGTATTTAT | 11169 |
rs113413396 | snp | C/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983456 | GGCGGGTGGATCACA[C/T]GAGGTCAGGAGTTCA | 11169 |
rs113449411 | snp | A/G | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962009 | CCTCAGCTAATTTTT[A/G]TATTTTTAGTAGAGA | 11169 |
rs113464615 | snp | G/T | 0.0655868 | 0.168795 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967660 | GGGTCTCACTGTGTT[G/T]CCCAGGCTAAAGCAC | 11169 |
rs113465964 | snp | G/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969834 | AAACCCAACAGTACT[G/T]TAGGAAGTTAATACA | 11169 |
rs113467865 | snp | C/G/T | 0.00498401 | 0.0496724 | synonymous-codon, missense | WDHD1 | GRCh38.p7 | 14:54989171 | TATGGCATTGTCTTG[C/G/T]TCATCATTATAGCAG | 11169 |
rs113469889 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948979 | CAAACAAAAAGGACA[A/T]CCATACCAAAACCCC | 11169 |
rs113486298 | in-del | -/G | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958038 | TTATTGGCCCCTAAA[-/G]TCTCCCAACTTAAAA | 11169 |
rs113512152 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022656 | CACTGCACTCCAGCC[A/G]GTGAGACAGCTAGAC | 11169 |
rs113520981 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007465 | TAAAGGTTCTTCAAA[C/T]CAATATATATCTCAG | 11169 |
rs113559747 | snp | A/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004756 | GCGAGCCCGACCCAA[A/T]GTTTATTTTTCATCA | 11169 |
rs113581900 | snp | A/C | 0.0611083 | 0.163768 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014050 | AAAAATAAAGTGCTA[A/C]TTTCCTTCTATAAAA | 11169 |
rs113592281 | snp | C/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000033 | TATTAAGTCTGCAAT[C/T]TGTAACCAGAAGTCT | 11169 |
rs113609480 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54995142 | ACGTGCCACCACACC[C/T]AGCTAATTTTTGTAT | 11169 |
rs113647221 | snp | A/G | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952759 | ACAAAACAGCACAGT[A/G]CTGGTACCAAAACAG | 11169 |
rs113647648 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996948 | AGGCGCATGCCACCA[C/T]GCCCAGCTAATTTTT | 11169 |
rs113669034 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962329 | TTTTATAAACATCTG[C/T]TAAATGACCATAGCT | 11169 |
rs113680438 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001901 | GTTAAATCTGACTTC[C/T]TATAACAAAGACCTA | 11169 |
rs113695652 | snp | C/T | 0.370772 | 0.218893 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003487 | GCCACTGCACTCCAG[C/T]CTGGGCAACAGAGTG | 11169 |
rs113777755 | snp | A/G | 0.139903 | 0.224452 | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938504 | ATGCCATTGCACTCC[A/G]GCCTGGGCAACAGAA | 11169 |
rs113781960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954218 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 11169 |
rs113799610 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997561 | ACCATTCCATTTATA[C/G]TCCTAAAAGTTTGTG | 11169 |
rs113871014 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | WDHD1 | GRCh38.p7 | 14:54956778 | TTGTTTTTTTCAGAT[A/G]GGGTATCTCTTATGT | 11169 |
rs113889192 | snp | A/G | 0.5 | 0 | missense | WDHD1 | GRCh38.p7 | 14:54962961 | TCTTACCCAGCATTC[A/G]GCTTTTTTCTGAAAT | 11169 |
rs113894527 | snp | C/G | 0 | 0 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028127 | TTTTATTACCTGAGA[C/G]GTTTTTCTGTTGAAG | 11169 |
rs113907952 | snp | A/T | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006878 | TTTTAAAAAGTAATT[A/T]AAAAAACTATTTTTA | 11169 |
rs113912754 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54952364 | CAGACAAACAGAGAG[C/G]CAAATCATGAGTGAA | 11169 |
rs113961629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958195 | GCAATGGTGTGATCT[C/T]GGCTCACTGCAAAGT | 11169 |
rs113964065 | in-del | -/A | 0.476691 | 0.10541 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983681 | CCTAATTTATTCCTT[-/A]AAAAAAAAAAAATTT | 11169 |
rs113966992 | snp | C/G | 0.5 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014647 | GCTTTTACTCATTTA[C/G]TATGTGCCCTATCTA | 11169 |
rs113970249 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54982150 | TAGCTGGGACTACAG[A/G]CACCCGCCACCACGC | 11169 |
rs114011474 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946485 | ATTAAATTATCAATC[A/T]TCTTTGTTGTTGTTT | 11169 |
rs114012401 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005073 | TGCTCTTCTTTTTCA[A/G]TCTCCTCAGGAACAC | 11169 |
rs114136655 | snp | A/T | 0.0584853 | 0.160693 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996791 | ATAAACTTTTTATTT[A/T]CATTTATTTATTTTT | 11169 |
rs114177676 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | WDHD1 | GRCh38.p7 | 14:55023452 | AAATTGTGAGCAACC[A/G]CAACTGCAGACCTCA | 11169 |
rs114177860 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960171 | TCTGTAGTTTGTTTG[C/T]TTATTTATTTATTTG | 11169 |
rs114259726 | snp | A/G | 0.0123181 | 0.0775069 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54944434 | CAAAATATTACTTCT[A/G]TTTTCTTCTAACCAC | 11169 |
rs114263040 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019878 | CATCTCAACAAAAAA[G/T]AAATCCGCTATCAGT | 11169 |
rs114269611 | snp | C/T | 0.00415443 | 0.0453867 | intron-variant | WDHD1 | GRCh38.p7 | 14:54956999 | CAAACAGATCCCATG[C/T]TGCTTACTGCAGATG | 11169 |
rs114290050 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024407 | TTCAGAAATGTAGAC[A/G]TTATCCCTGTTGCCT | 11169 |
rs114298834 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014461 | AATAAAATAGGGACC[A/G]TATCTTCCTTGTCCA | 11169 |
rs114300699 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971998 | TTCAGACCAGCCTGG[A/G]CAACATGGCAAGACA | 11169 |
rs114492851 | snp | A/T | 0.00145265 | 0.0269112 | synonymous-codon, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000978 | ACAGGGAGACCAGGT[A/T]ACTATATTGAGGGTC | 11169 |
rs114512008 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006942 | GGTTAAAAATAAGAA[C/T]CATGCCAGGCACGGT | 11169 |
rs114520145 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54978239 | CTAGATTCCTGAAAA[C/T]GGACATGCAAGAAAT | 11169 |
rs114619759 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54963900 | AGGGACTGCTAGAGG[A/C]CAGGAGTTTGAGACT | 11169 |
rs114641135 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018086 | CTCTGCTTGGAGTGA[A/T]TGGGTTTTTAAAATC | 11169 |
rs114681846 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971168 | ATACCCTTCAGGATA[C/T]TGGCCTTGGTAAATA | 11169 |
rs114719842 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966849 | AGCTATCATAATTAA[C/T]GCTCAGAGAATTTGG | 11169 |
rs114849309 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943225 | TTATCAGAAGCAAGC[C/G]AGCCACCTGTCCTAA | 11169 |
rs114849418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026919 | CGCAGCCCGGTTTCC[C/T]CCACCCGAGTGACAC | 11169 |
rs114853027 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995477 | AAAGTCATTTAATGC[G/T]ATAAAATTTCCTCTA | 11169 |
rs114858242 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987479 | TATTCAACAAAAAAA[A/C]CAAATAGTTTACTTC | 11169 |
rs114905095 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018150 | ACAACCTAAGTGTCC[C/T]ACTGTAATAATGGTA | 11169 |
rs114911405 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955417 | TATTTGTGGCTTCCT[C/T]ATAGTCACAAGTGTC | 11169 |
rs114955732 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016051 | GGAGACGTACAAAGT[C/T]ACAGGTGCCAGTTGG | 11169 |
rs114963628 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974206 | GTAGGCAGATCGCTT[C/G]AGCTCAGGAGCTCAA | 11169 |
rs115022805 | snp | G/T | 0.00278641 | 0.0372215 | missense | WDHD1 | GRCh38.p7 | 14:54941681 | CTCCTTTGGCTTTGT[G/T]AGCCCACACCTTTGT | 11169 |
rs115048907 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54976568 | CTACTAAAAAAGTGA[C/T]TGCAGAATTTTATTC | 11169 |
rs115080665 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944997 | GATCACTCACGTTTG[C/T]ATTTTCCAAGTGCAG | 11169 |
rs115082821 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984973 | TAGACTGACTAGCAC[C/T]ACTTTTTATGAATAA | 11169 |
rs115136072 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954489 | CCATACATGAATCCA[C/T]CTTATAGCTATATAT | 11169 |
rs115182445 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969668 | TCCTACTGAAAATAT[A/T]CCAAAATACCAACTC | 11169 |
rs115185521 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983672 | AGCAAGACTCCTAAT[C/T]TATTCCTTAAAAAAA | 11169 |
rs115186442 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998672 | TGTTTAACAGATCCT[A/C]TTAACTTCCATCTAT | 11169 |
rs115239906 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971461 | ATGTGCCTGTAGTCT[C/T]GTGCAATCCCATTTA | 11169 |
rs115324363 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967039 | TCCTGAGAGTAAGTC[C/T]TTCCCCAGTGGGTCT | 11169 |
rs115338846 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001482 | TGCCCAAGTTGGTTT[C/T]GGATTCCTGGCCTCA | 11169 |
rs115341226 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979191 | GATAGGTTCTCTGTC[A/G]CCTAGACAGGAGTGC | 11169 |
rs115400458 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991935 | AAGAAAAAATAACTG[A/G]CAGAATTTGTTGCCA | 11169 |
rs115650875 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021693 | GCCCAGCCATGTCTG[C/T]TACCTCTTGAATGTC | 11169 |
rs115651052 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54968591 | TGATTTTTTGAAAGG[A/T]TAAACAAGATCGATA | 11169 |
rs115673688 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:55023551 | GAGTATGTCCAGCAT[C/T]ACTAGTGGCACTTCA | 11169 |
rs115754470 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988316 | TGGCCAAGGCTCAGG[C/T]TGAATTAACTGCAAA | 11169 |
rs115758310 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959684 | GAGGCAGGAGGATCA[C/G]CTGAGCATACGAGTT | 11169 |
rs115780835 | snp | A/C/G | 0.0655868 | 0.168795 | intron-variant | WDHD1 | GRCh38.p7 | 14:54978038 | AAATTGTTCATTGCA[A/C/G]ATGACTAATTTCATA | 11169 |
rs115832415 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025565 | GCTCCTTTTCCAATT[A/C]ATCCTCCATGCATTT | 11169 |
rs115834293 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | WDHD1 | GRCh38.p7 | 14:54973108 | AGCACTGGAAAACCA[A/T]GACTGCACACTATAA | 11169 |
rs115907350 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014678 | CACACATACAAAAAA[A/G]CAAATAAAAACACAA | 11169 |
rs115935300 | snp | A/C | 0.0123036 | 0.0774623 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940751 | CAATACTGTCACAGC[A/C]GTGTCTTCAGTTCTT | 11169 |
rs115947628 | snp | A/C/G/T | 0.00296141 | 0.0383663 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000619 | ATGCCAGACCACAAA[A/C/G/T]TGCATAACCTTTCTC | 11169 |
rs115968042 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988141 | CTACCTATTTACTTA[A/C]CTACCTACTTATCAA | 11169 |
rs116076641 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993829 | GTGAATAAATATTTT[A/T]AAATTTCTGAATTTT | 11169 |
rs116117710 | snp | A/G/T | 0.00334213 | 0.0407424 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55008320 | GCTGAGTTTACCTGA[A/G/T]CTGAAATTTGCCACA | 11169 |
rs116121327 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995309 | CAAAGAACCAGCTTT[C/T]GGTCTCATTGACTTT | 11169 |
rs116125239 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967499 | AGAATAGTAATATTA[C/T]AATAGCTGCCTTAAT | 11169 |
rs116134820 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55029094 | CTAGTATCATGTTTT[C/T]ACAATTCCATTTGTT | 11169 |
rs116255253 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | WDHD1 | GRCh38.p7 | 14:54973302 | TTTTATAAATATCTT[C/T]CAGTATTATCAAATG | 11169 |
rs116383181 | snp | A/T | 0.0955749 | 0.196603 | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938709 | AATGAGTTGTGACTG[A/T]GCCACTGCACTTCAG | 11169 |
rs116442480 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962419 | GCCTTAAGAGTTAAG[A/G]TGTATTTGCGTAGAT | 11169 |
rs116577421 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024141 | CACGTATAAGTAGAC[A/T]TACACAATTCAAATT | 11169 |
rs116592265 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960577 | TGATCTCCACTTACT[C/G]CAACTCCCCACTCCT | 11169 |
rs116593701 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944112 | TTAGTTGTCATGATC[A/G]TTATTATCTTTGTTG | 11169 |
rs116598172 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987994 | ATCAGTACTATAATC[A/T]GCTGAAGAAGGGATC | 11169 |
rs116607580 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969711 | CTCTATAAAGCCAGC[A/G]TTATCCTGATACCAA | 11169 |
rs116694262 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991069 | AACCATAAAATAAAC[C/G]AACCACAAAACTGTA | 11169 |
rs116812242 | snp | C/T | 0.00676609 | 0.0577691 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939123 | CTGTCAAATTTCAAA[C/T]TTTCTGTAGGTTTGA | 11169 |
rs116865153 | snp | A/G/T | 0.00398564 | 0.0444627 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969985 | GCAGAAAAAGCTTTC[A/G/T]ATAAAATTCAACATC | 11169 |
rs116867150 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996467 | TAGCCAGGCATGGTG[A/G]CATGTGTCTATAGTC | 11169 |
rs116881417 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955008 | TGCTGAGATTATAGG[C/T]GTGAGCCACCATGCC | 11169 |
rs116886179 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021676 | CAGGTGTGAGCCACC[A/G]CGCCCAGCCATGTCT | 11169 |
rs116910655 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954037 | AATGATGAGCACAGC[A/G]CACCAACATGGCACA | 11169 |
rs116981342 | snp | C/T | 0.0360663 | 0.129354 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028298 | GCTGAGGTTTGTATA[C/T]GAATGAAGAGGAAGA | 11169 |
rs117021459 | snp | C/G | 0.0448719 | 0.142907 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967468 | AATTTAAAAAGTTTT[C/G]AAAAGTTAGTAACTT | 11169 |
rs117070457 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960502 | AATTTTTATTTACTT[A/C]TTCTTATTATTATTT | 11169 |
rs117103315 | snp | A/T | 0.0479149 | 0.147179 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957378 | TTCCCAAATACCACA[A/T]CCCCAAGAAAGACAG | 11169 |
rs117124038 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943141 | CTGAGGATTTAACTG[C/G]TACACCACACACATT | 11169 |
rs117201589 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948076 | CAAAATTAAGCGGTT[C/T]CAAGATGGTCGAATA | 11169 |
rs117236077 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999069 | GAAACTCTCTCTTTA[C/T]GTCTTTTCTCTTAGA | 11169 |
rs117273767 | snp | A/G | 0.0705729 | 0.174086 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000683 | AAAAATACTGTCAAG[A/G]AAAATATAAATTGTA | 11169 |
rs117298779 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | WDHD1 | GRCh38.p7 | 14:55012704 | AGGGTCTTCTTATTG[C/T]ATCATCCCATCTTGG | 11169 |
rs117301751 | snp | G/T | 0.0448719 | 0.142907 | intron-variant | WDHD1 | GRCh38.p7 | 14:54965450 | AAAGGCAGGCATATC[G/T]AACAGCCCGATCAAA | 11169 |
rs117314452 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022485 | TAAAAACCTGTTCAC[C/T]AGCCTGGCCAACATG | 11169 |
rs117316271 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019885 | ACAAAAAAGAAATCC[A/G]CTATCAGTGTCTGGG | 11169 |
rs117327442 | snp | A/T | 0.0448719 | 0.142907 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964818 | CCCTGGTATTTTTGA[A/T]ATGAGAAACACTGCC | 11169 |
rs117401558 | snp | C/T | 0.021333 | 0.101051 | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938574 | GCCTGGGCAACATGA[C/T]GAAACCCATCTATGT | 11169 |
rs117403611 | snp | A/C | 0.0475351 | 0.146656 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943095 | TACTAGGTGCCTGTG[A/C]TGCGCCCTGCCATTC | 11169 |
rs117428315 | snp | A/C | 0.0437281 | 0.141251 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998769 | CCGACCCCAATTCTC[A/C]CAATATAGATAGATA | 11169 |
rs117432389 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948326 | GCTGTGACACACAGC[A/G]CCTGGAAAATTGGGT | 11169 |
rs117444046 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984054 | GTTATTGTAGTAAAC[A/G]GTGAAGCTCTAGAAA | 11169 |
rs117513209 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999332 | TCTCCAACATTCTGC[C/T]AGAATGCATGTGAAG | 11169 |
rs117528782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991503 | ATTCATATTCAATGA[C/T]ACTGACATGCTATTT | 11169 |
rs117546374 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946823 | CCGAGATGGGCAAAT[C/T]GCTTGAGGCCAAGAG | 11169 |
rs117607892 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021713 | TCTTGAATGTCTCCA[A/G]GGTCTATATCTTGAA | 11169 |
rs117609468 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022338 | AGTTCTGATCACAAA[A/T]CTGATTGTATTTGCA | 11169 |
rs117649156 | snp | C/T | 0.029116 | 0.117091 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957295 | AAATTTCTGTTAAGT[C/T]TGTATTGCCATCTCA | 11169 |
rs117679429 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007580 | AAATCTTAAATAACT[A/G]GAGTATTTTCTGTGC | 11169 |
rs117690026 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005313 | GATCAGCACTGGGAT[C/T]AGTCACCATAAGAAG | 11169 |
rs117745004 | snp | G/T | 0.0327778 | 0.123752 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002373 | ACTCCTGGGTTCAAG[G/T]GATCTTCCTGGCTCA | 11169 |
rs117821150 | snp | C/T | 0.000333923 | 0.012917 | missense | WDHD1 | GRCh38.p7 | 14:54963022 | TTGCTGTCAATTCGG[C/T]TGCCTTCTCTACAGC | 11169 |
rs117867527 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999839 | CTCAAACTCCTGGGC[C/T]CAAGCAATCCTCCCA | 11169 |
rs117894181 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:55023646 | GAATCACCAGAGATG[A/T]CTTTTTACTGGGATA | 11169 |
rs117900750 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:54968555 | AGAATCCATACAAAG[A/G]ATCAATAAAACAAAA | 11169 |
rs117933520 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016427 | CCACGGGGCTACAGT[C/T]ATACTATAGTGATAA | 11169 |
rs117958211 | snp | G/T | 0.0667028 | 0.170006 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988711 | TTTTTTTCTTTACAA[G/T]GAATGTATATTACTC | 11169 |
rs118038899 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991977 | TGAGCTTTCAGGCCA[A/G]GCACGGTGGCTCACA | 11169 |
rs118111298 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947562 | GAAAAATGAGATATA[C/T]TATGGTAAAAATGAA | 11169 |
rs118135200 | snp | A/T | 0.0433465 | 0.140692 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002758 | TACAGCCCAACTAAT[A/T]TTTTTCCTGTTTTTT | 11169 |
rs137954627 | snp | A/C | 0.0624933 | 0.165354 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944506 | AAACATTTTATACTT[A/C]AGACAGAGTTTAAAG | 11169 |
rs137965013 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971543 | GGTGAAAGATCTCTA[C/T]AAGAACTACAAAACA | 11169 |
rs137977906 | snp | A/G/T | 0.000100625 | 0.00709248 | synonymous-codon, splice-acceptor-variant | WDHD1 | GRCh38.p7 | 14:54957631 | GCTGCTAAAGGTAAC[A/G/T]GCACCTTTCACAAAA | 11169 |
rs138009284 | in-del | -/TTTC | 0.0655868 | 0.168795 | intron-variant | WDHD1 | GRCh38.p7 | 14:54976229 | AAATATGAAGATGAA[-/TTTC]TTTATTTCCTTTTTA | 11169 |
rs138023039 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947383 | TATGCCCGGCCTATC[A/G]ATTTTCTTAAATAAA | 11169 |
rs138036839 | in-del | -/TCT | 0.00200418 | 0.0315923 | cds-indel | WDHD1 | GRCh38.p7 | 14:54962976 | AGCTTTTTTCTGAAA[-/TCT]TCTTCTTCTTCTTCC | 11169 |
rs138075418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005588 | TAGATGTACTGTCCC[A/G]TCTGGAAGACAAAGC | 11169 |
rs138076157 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988792 | CCATCTCTTGCATTA[C/T]TAACTATGCCATGTC | 11169 |
rs138097867 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015077 | AGGAGGACTATAAGT[C/T]TCAGTTTGCCTGAGA | 11169 |
rs138138622 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949164 | GGAGAATGACTTTGA[C/T]GAGTTGAGAGAAGAA | 11169 |
rs138144098 | snp | C/G | 1.64749e-05 | 0.00287005 | missense | WDHD1 | GRCh38.p7 | 14:54989103 | ATTGTATAATTCAAA[C/G]TGTTTGATAAGTGTG | 11169 |
rs138189016 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54978613 | CCGTTAATGAATATA[C/T]TTCTTCTGATACTAA | 11169 |
rs138207824 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972949 | CTAAACCTGTTCTGA[A/G]TAGTCTATATAAGGC | 11169 |
rs138254684 | in-del | -/TAAAT | 0.0869419 | 0.189505 | intron-variant | WDHD1 | GRCh38.p7 | 14:54990084 | TATTTAACATAACTA[-/TAAAT]AAAATATTGACACTA | 11169 |
rs138273571 | in-del | -/A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54980801 | AAAAAAAAAAAAAAA[-/A/T]CTCAGCTGGGCGTGG | 11169 |
rs138284824 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949290 | AACTAGAATAACCAG[C/T]GTAGAGAACTCCTCA | 11169 |
rs138294746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015738 | CAGTCTCACTCTGTC[A/G]CCCAGGCTGAAGTGC | 11169 |
rs138298438 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959899 | TTCCCCTTTTGTCTC[A/T]CCTGGCAGAGTGCTA | 11169 |
rs138340558 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954815 | GATGACTGCAATCTC[C/T]GCGTCCCGGGTTCAA | 11169 |
rs138403748 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958612 | CTTGTTTGCTCTATC[A/G]ATGGCATCCCACATA | 11169 |
rs138410771 | snp | A/T | 0.00826952 | 0.0637681 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55002094 | TTTGTAAAACCTACC[A/T]GAGAGATGAAATTAT | 11169 |
rs138428547 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944020 | TATTACCATATATCC[A/G]CACTTACTTTCCTCT | 11169 |
rs138433810 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007583 | TCTTAAATAACTAGA[A/G]TATTTTCTGTGCAGA | 11169 |
rs138439609 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939652 | AGAAATAAGGATAAT[A/G]TTTCTTGGTTTCAAA | 11169 |
rs138443799 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004218 | CTGGTATTCATATCC[C/T]TGTGCTAATACATTT | 11169 |
rs138529728 | snp | C/T | 0.021333 | 0.101051 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996826 | AGAGTGGAGTCTCGC[C/T]CTGTCGCCAGGCTGG | 11169 |
rs138559000 | snp | A/G | 1.6501e-05 | 0.00287232 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000965 | CTAAATATTGCCCAC[A/G]GGGAGACCAGGTTAC | 11169 |
rs138574897 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962087 | TTATCCGCCCACTCC[A/G]GCCTCCCAAAGTGCT | 11169 |
rs138625438 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947612 | TTTTGTTTTTTCTGA[C/G]ATGGAGTCTCACTCT | 11169 |
rs138695428 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972439 | AAAAATTAGCTGGGT[A/G]TGGTGGTGAACGCCT | 11169 |
rs138702761 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952225 | TTGCAGATGACATGA[C/T]TGTATATTTAGAAAA | 11169 |
rs138713030 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019415 | TGTCAATGTATTCAC[A/G]TATTTTGAAGCCTAT | 11169 |
rs138735219 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977000 | TTCTACAACAAGCTG[G/T]TCTTTATAGGAGAAG | 11169 |
rs138790271 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016171 | TTAGAGTAGTCTGAA[C/T]GTTTTTCTAAATGGT | 11169 |
rs138807592 | snp | C/T | 0.0803491 | 0.183626 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952466 | CTTCAAAGAGAACTA[C/T]AAACCACTGCTCAAT | 11169 |
rs138807885 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55013168 | GAGTTTGAGACCGGT[C/T]TGAGCAACATGGCAA | 11169 |
rs138866202 | in-del | -/A | 0.0599851 | 0.162463 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014914 | AGAGAAAACCACATG[-/A]AAAAAAATATAGTTA | 11169 |
rs138884409 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019850 | CTCCAGCCTGGGCGA[C/T]AGAGCTAGACTCCAT | 11169 |
rs138912927 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:54968841 | AGGTCAGAAGTTTGA[C/T]ACCACCCTGGGCAAC | 11169 |
rs138913640 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996942 | GACTACAGGCGCATG[C/T]CACCATGCCCAGCTA | 11169 |
rs138914907 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011885 | CCTTCAATTGTTTCC[A/G]ACATTTGCTATTGTT | 11169 |
rs138925337 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54972591 | AAAAAAAAAAAAAAA[-/T]GCCAATGAGGCATAT | 11169 |
rs138947597 | snp | C/T | 0.0018782 | 0.0305871 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955513 | GTATTGCTGCTACTG[C/T]ATACTTTTTACTTGG | 11169 |
rs138953223 | snp | A/C/G | 0.0138852 | 0.0822049 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008883 | TCAACTGCAACCTCC[A/C/G]CCTCCCAGGTTCAAG | 11169 |
rs139052310 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994298 | TCTATTTCATTTAAG[C/T]TGTTAAATTTATGGG | 11169 |
rs139061011 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963421 | AAAGTAATGGTGCAC[C/T]ATGCAATAAACAGTG | 11169 |
rs139076141 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54992006 | CACCTGTAATCCCAG[C/T]ACTTTGCAAGGCCGA | 11169 |
rs139081958 | snp | C/G | 1.70235e-05 | 0.00291744 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55008356 | ACAGATCCATCACAA[C/G]TAGCTGATGCCTGCA | 11169 |
rs139106534 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953756 | GACTAGATTAAGAAA[A/G]TGTGGCACATATACA | 11169 |
rs139110535 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021737 | TCTTGAAATTACTTC[A/G]CTCCCTTATCTTTTT | 11169 |
rs139120430 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998970 | AACCCCAAGTGGTTG[G/T]CATTATTCCTATCTT | 11169 |
rs139293739 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974297 | AATTTGCTAGGCATG[A/G]CAGCATGGACCTGTA | 11169 |
rs139322894 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028130 | TATTACCTGAGACGT[C/T]TTTCTGTTGAAGAGG | 11169 |
rs139338802 | snp | C/G | 0.000153988 | 0.00877328 | utr-variant-5-prime, missense | WDHD1 | GRCh38.p7 | 14:55013582 | TCACCATCACTTCCA[C/G]AAGTCACAATAAAAC | 11169 |
rs139363075 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55023950 | TTTATAATAGATTTG[C/T]GTATATTTTATGGTA | 11169 |
rs139365985 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54943794 | AAACAGTAAACCGTC[-/A]AAAAATTAACCATCC | 11169 |
rs139399115 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981752 | TGTTGTTAAAGGAAC[C/T]CTATTTCAAATATAT | 11169 |
rs139419687 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016768 | TACTGTATTGGACAG[C/T]GCAGCATTAAAAGAA | 11169 |
rs139440460 | snp | C/T | 0.00718502 | 0.0595053 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000983 | GAGACCAGGTTACTA[C/T]ATTGAGGGTCTGTAA | 11169 |
rs139446895 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026115 | TGTGTCTGGTTCGCT[C/G]TATTCTATCTGTAGT | 11169 |
rs139462255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009724 | GGCATGAGCCACGAC[A/G]CCAGCCCTAAAATAA | 11169 |
rs139522683 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | WDHD1 | GRCh38.p7 | 14:54990366 | ACTTTGGGAGGCCTA[A/G]GCAGGCGGATCACGA | 11169 |
rs139553099 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54985433 | GAAGAATGGAGGGCT[A/C]GAAGAACACAAAGAG | 11169 |
rs139562239 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946958 | TGAGGCATGAGAATT[C/G]CTTGAACCCAGAAGG | 11169 |
rs139590727 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | WDHD1 | GRCh38.p7 | 14:54941943 | AAAATACTATAATTG[C/T]AGTACTATTTAAAAA | 11169 |
rs139632055 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:55012789 | GATGAACCCACTCCT[C/G]AGATGGTGGCATCAA | 11169 |
rs139669547 | in-del | -/AAAT | | | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938754 | GAGACCCTGTCTTTA[-/AAAT]AAATAAATAAATAAA | 11169 |
rs139731967 | snp | A/C | 0.0126979 | 0.078662 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941201 | CTTTAATGATTTTTC[A/C]AGGTTAAGAAACAAA | 11169 |
rs139751226 | snp | C/T | 4.95413e-05 | 0.00497677 | missense | WDHD1 | GRCh38.p7 | 14:54963078 | ATTAATTTCCGAGAG[C/T]GAGAAGCATATTTAA | 11169 |
rs139755196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009291 | TTGCTAATCTAATTA[C/T]AGCTACAACCATTTT | 11169 |
rs139758936 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946074 | AGTAAAAATCAAGGT[A/G]TAACAAAGGTTCCTG | 11169 |
rs139790795 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | WDHD1 | GRCh38.p7 | 14:54956827 | ACTCCTGGGCTCAAG[C/T]GATCCTCCCACCTCA | 11169 |
rs139807986 | in-del | -/ATATAT | 0.159836 | 0.243547 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987437 | TCATATGATATTTAC[-/ATATAT]ATATATATATATATA | 11169 |
rs139876753 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960268 | TGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT | 11169 |
rs139969304 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998836 | GGTTATTAAGATCAT[G/T]TAAATGCTATTCATG | 11169 |
rs139971624 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948486 | GATTGAACTACAAGG[C/T]GGCAGCCTCAGCCAG | 11169 |
rs139974566 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002695 | ACTGAGCCTCAAACT[C/G]CTGGGGTCAAAGGAT | 11169 |
rs139980908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994621 | CAAAAATTAGCCAGG[C/T]GTGGTGGCGCATGCC | 11169 |
rs140011673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984648 | ATTAGGAATAAAACA[A/G]TGAAATAATTTTCTT | 11169 |
rs140023951 | in-del | -/TA/TATATATA/TATATATATATA/TATC | 0.487158 | 0.264714 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003587 | GAAAGAAAAACGAAC[lengthTooLong]CTATATATATATAGT | 11169 |
rs140038782 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989995 | ATACCACTTGGAAAA[C/G]TTATCTTCCACTGAT | 11169 |
rs140040926 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948802 | GGTACCCCTCTGAGA[C/T]GAGGCTTCCAGAGGA | 11169 |
rs140087865 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54980664 | CAAAAATTAGCTGGG[C/T]ATGGTGGCACATGCC | 11169 |
rs140172495 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952787 | CAGAGATACAGACCA[A/G]TGGAACAGAACAGAG | 11169 |
rs140174391 | snp | C/T | 8.25866e-05 | 0.00642546 | missense | WDHD1 | GRCh38.p7 | 14:54941591 | CTTTTGCTTTTTCTT[C/T]CTGGTTTTCTGTTTC | 11169 |
rs140179190 | snp | A/C/T | 0.0130663 | 0.0797659 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013450 | ATCACATGCCAGTAT[A/C/T]ATTTCATATCAATTG | 11169 |
rs140186646 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010964 | AAGGAATGTTGAGGA[C/T]TGCCACACCACCAGA | 11169 |
rs140213800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949564 | GAGAATGGAACCAAG[C/T]TGGAAAACACTCTGC | 11169 |
rs140230532 | in-del | -/AAAT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54942252 | AGACTCCGTCTCAAA[-/AAAT]AAATAAATAAATAAA | 11169 |
rs140237656 | snp | C/G | 3.3012e-05 | 0.00406262 | missense | WDHD1 | GRCh38.p7 | 14:54987376 | GAACTAAAGTGCAGG[C/G]AGTGAAGCTTGCTAA | 11169 |
rs140324706 | in-del | -/TTCAGA | 0.428484 | 0.175052 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955876 | ACCAAAAAACTACAC[-/TTCAGA]TTCAGATTCCATGTT | 11169 |
rs140326760 | snp | A/G | 0.0861826 | 0.188849 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022637 | CAGTGAGCTAAGATC[A/G]CGCCACTGCACTCCA | 11169 |
rs140346069 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019741 | AGCTGTTGCGGAGGG[A/C]ATCTGTGATCCCAGC | 11169 |
rs140392395 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949045 | ATGAAACCATAAAGA[C/T]TGGGGAAAAAACAGA | 11169 |
rs140400066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017340 | CTGTAGGAAAAATCA[A/G]TATTCTTTTTTTTTC | 11169 |
rs140401473 | snp | A/C | 0.000399281 | 0.0141238 | missense | WDHD1 | GRCh38.p7 | 14:54957133 | CTTGGATGATTTGCC[A/C]ATATTGTCTAAAATA | 11169 |
rs140402955 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | WDHD1 | GRCh38.p7 | 14:54990489 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 11169 |
rs140425226 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | WDHD1 | GRCh38.p7 | 14:54965721 | AGCACTTTCGGAGGC[C/T]GAGGCAGGTGAATTA | 11169 |
rs140442475 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988089 | AAACATTCTGCACCC[A/G]TTGCTTTCCCATCAT | 11169 |
rs140464187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006196 | ATGTTATCAAAACTA[C/T]AGATTAATTTAGGGA | 11169 |
rs140515064 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954698 | ATTTACTTTTTCTGA[A/T]AGCCTTGCTATAGTA | 11169 |
rs140603626 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006945 | TAAAAATAAGAATCA[C/T]GCCAGGCACGGTGGC | 11169 |
rs140606197 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988882 | GTTCTGAGGTATTTT[A/G]GGTGTGCTGGTGTTT | 11169 |
rs140633854 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963725 | GAATCGCTTGAACCC[A/G]GGAGGTGGAGGTTGC | 11169 |
rs140638639 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971169 | TACCCTTCAGGATAT[G/T]GGCCTTGGTAAATAT | 11169 |
rs140671376 | in-del | -/TC | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954723 | ATAGTATAAAGAAGT[-/TC]TTTTTGTTTTTTTGG | 11169 |
rs140770200 | snp | C/G | 0.00196339 | 0.0312704 | missense | WDHD1 | GRCh38.p7 | 14:54984809 | TGTTTTTTCTTTTTC[C/G]CCAGCTCTAGCAGTT | 11169 |
rs140777365 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54976423 | GCTAGCCTCAAACTC[A/C]TGGCCTCAAGTGATC | 11169 |
rs140795694 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964253 | CAAAAGCTTTAGATA[A/T]TCACCTGGATGCCCT | 11169 |
rs140876352 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982332 | TTTTAAAGCCAATTT[C/T]AGTAAAAAATTAAAC | 11169 |
rs140877260 | snp | A/T | 0.000382463 | 0.0138234 | synonymous-codon, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000626 | ACCACAAATTGCATA[A/T]CCTTTCTCATGTTTC | 11169 |
rs140881679 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020849 | TATGTATTATATACT[A/C/G]TATCTGTACAATACA | 11169 |
rs140885882 | snp | C/T | 0.00108722 | 0.0232901 | missense | WDHD1 | GRCh38.p7 | 14:54981669 | AGCATTCGAACAATT[C/T]CTTCTGAATCCACGT | 11169 |
rs140897241 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018723 | TTTGCTCTGAGCCTG[C/T]CAAGTACCTTAGAAC | 11169 |
rs140911735 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002941 | TGATATAAAAATTCC[A/T]CCCATTTGTTTGAGG | 11169 |
rs140961762 | snp | A/G | 0.000428484 | 0.0146307 | missense | WDHD1 | GRCh38.p7 | 14:54991269 | GAAATGGCTTTTGCC[A/G]GGGAGTTGGCATGGG | 11169 |
rs141000933 | snp | C/T | 3.30355e-05 | 0.00406407 | missense | WDHD1 | GRCh38.p7 | 14:54991392 | AACCAGTTTTTAGCA[C/T]TGAAATATCTACAAC | 11169 |
rs141022693 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943770 | ACATACAGGAACTTA[C/T]AGAGATTAAAACAGT | 11169 |
rs141057912 | in-del | -/G | 0.139903 | 0.224452 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979290 | CAAGTAGCAGAGACT[-/G]ATAGGTGTGTGCCAT | 11169 |
rs141076168 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977310 | ACCATGAATTGTCTG[C/T]AGACCAAATACAAAA | 11169 |
rs141126548 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940299 | AATCTGGCTTTGGAA[C/T]CTGTGCTCATAACCA | 11169 |
rs141132123 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005202 | CTCCCTTGCTGTTGC[A/T]TGGGATGGTAGTGTC | 11169 |
rs141140861 | snp | C/T | 0.000692019 | 0.0185884 | missense | WDHD1 | GRCh38.p7 | 14:54989158 | GGAACTCCACATCTA[C/T]GGCATTGTCTTGCTC | 11169 |
rs141225640 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947315 | TGCATTGCAGTCTGG[A/G]CAACAAGAGCAAAAA | 11169 |
rs141241177 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945715 | CCAGCTAATTTTTGT[A/G]TTTTTAGTAAAGACA | 11169 |
rs141262964 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982256 | CCTTGTGATCCACCC[A/G]CCTCAGCCTCCCAAA | 11169 |
rs141263478 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54980441 | CCCATGCCACACCCA[C/G]CCAATGTATCATTTT | 11169 |
rs141419326 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949433 | TGAATGAAATGAAGC[A/G]AGAAGAAAAGTTTAG | 11169 |
rs141423225 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | WDHD1 | GRCh38.p7 | 14:54970270 | ATATTACTCTATACA[C/T]AGAATTGCTAAAGGG | 11169 |
rs141432184 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014514 | CAGTCTCTGACAGAA[A/G]CCTTAATAAATGTTT | 11169 |
rs141461049 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966057 | AGAATGGCTGGGTGT[A/G]GTGGCTCACACCTGT | 11169 |
rs141466064 | snp | G/T | 1.65083e-05 | 0.00287296 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54991240 | AGTGAGATGCAACGG[G/T]GTAGAACCTGACTGA | 11169 |
rs141493145 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960269 | GCCTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC | 11169 |
rs141507899 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999482 | ATTCTGAATCTCTGG[A/G]GATTCAGTGAGGCAA | 11169 |
rs141575552 | snp | G/T | 1.65531e-05 | 0.00287686 | utr-variant-5-prime, missense | WDHD1 | GRCh38.p7 | 14:55010325 | TAGATCCAGCAGCAA[G/T]TTTAGTACCATCCCC | 11169 |
rs141594372 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959789 | CTGTATCCGCACCCC[A/C]CCCACCAAACAAAAA | 11169 |
rs141626115 | snp | A/G | 0.000403505 | 0.0141982 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54966565 | ATTTTTAGCTAAATA[A/G]TCAAGGTGGTTGTGA | 11169 |
rs141675860 | in-del | -/A | 0.0766824 | 0.180169 | intron-variant | WDHD1 | GRCh38.p7 | 14:54992198 | GGGAGACTCCGTCTC[-/A]AAAAAAAAAGAGCTG | 11169 |
rs141680216 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999129 | TCCTGCCTGAAATGC[A/C]TAAGAATGGCTGACA | 11169 |
rs141716711 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54973224 | AATTTATAGTATAGC[A/C]TTTTAATCAGGACAT | 11169 |
rs141726052 | in-del | -/CT | 0.0197687 | 0.0974348 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009514 | CTCAGCTCACGCAAC[-/CT]CTGTCTCCCGGGTTC | 11169 |
rs141735548 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55012588 | CTGTTCTGTACTGCT[A/G]TAAGAATCCCACAGA | 11169 |
rs141843920 | snp | A/G/T | 0.000230682 | 0.0107373 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54957112 | TCGACTAAGTGCAGT[A/G/T]GATTTCTTGGATGAT | 11169 |
rs141846565 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983914 | TATTATCATTTAACA[C/T]GTAATCAACATAAAA | 11169 |
rs141857558 | in-del | -/A | 0.479904 | 0.0982045 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969344 | AGACTCCGTTTCAAG[-/A]AAAAAAAAAAAAAAA | 11169 |
rs141887223 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952274 | AAATCTCCTTAAGCT[A/G]ATAGGGAACTTCAGC | 11169 |
rs141914015 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947565 | AAATGAGATATATTA[C/T]GGTAAAAATGAAATT | 11169 |
rs141933115 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011312 | AGGCGGGTGGATCAC[A/G]TGAGGTCAGGAGTTC | 11169 |
rs142033829 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020670 | CTGGAAGGTATCAGC[C/T]AAAGATGTAAAGGTG | 11169 |
rs142068499 | in-del | -/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55003752 | ATTTTCAGTAGAGAC[-/G]CGGGGTCTTATCATG | 11169 |
rs142070762 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983537 | AATTAGCCGAGTGTG[A/G]TGACGCAAGCCTGTA | 11169 |
rs142084141 | in-del | -/AAA | 0.0103295 | 0.0711199 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018562 | ATGAATTTTGTCCTT[-/AAA]AAAAACAGTGAAGAC | 11169 |
rs142090973 | snp | G/T | 1.65968e-05 | 0.00288065 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:54995699 | CATCATCATTTATAA[G/T]CCCTTTTGAAAAAGA | 11169 |
rs142102529 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014290 | AGACAGGGTGTCCCT[A/G]CGTTGCCCAGGCTGG | 11169 |
rs142138992 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994090 | CTATTTGAAGATTTT[A/C]AATTACAATCTCAAT | 11169 |
rs142240916 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998933 | TGTTCTAACTATACA[C/T]AATTCACTTAATCCT | 11169 |
rs142265623 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006857 | TCTAAAATTTATAAT[A/C]CAAATTTTTAAAAAG | 11169 |
rs142283365 | snp | A/G | 0.000962528 | 0.0219166 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54941565 | CTGCTTTTTAGACAA[A/G]TTCAGGTTCTCTTTT | 11169 |
rs142317813 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998145 | TTCAACCCAGGAGGC[A/G]GAGGTTGCAGGGAGC | 11169 |
rs142318391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958813 | CTCATTTTTCTTTTT[A/G]CTTTACATTCTCCCC | 11169 |
rs142329089 | snp | A/G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55027508 | GCTGCCTGGCCTCGC[A/G/T]GGCCGGGGTCTTGTT | 11169 |
rs142386283 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947037 | GACAGGGCAAGACTG[C/T]CTCAAAAAAAGTGTT | 11169 |
rs142416038 | snp | A/G | 6.59707e-05 | 0.00574291 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54981683 | TCCTTCTGAATCCAC[A/G]TAACAAGGGGTACCT | 11169 |
rs142447261 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959903 | CCTTTTGTCTCTCCT[A/G]GCAGAGTGCTAGCCC | 11169 |
rs142450321 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961345 | TAAAATAAAATAAAA[A/T]AAAGACCAAAATCCT | 11169 |
rs142488027 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000443 | AGTTTGTGGTGTCTT[C/G]CAAATCCATATGATC | 11169 |
rs142514170 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949189 | GAAGAAGGCTTCAGA[C/T]GATCAAACCTCTCCG | 11169 |
rs142517406 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018326 | GAAATTTATCCCTAC[A/G]AAAGCAAATAAGAAT | 11169 |
rs142540965 | snp | C/T | 3.29701e-05 | 0.00406005 | missense | WDHD1 | GRCh38.p7 | 14:54944357 | TCAGTTGACAATACT[C/T]TAAATCGAATCATTC | 11169 |
rs142576091 | snp | C/T | 0.000795176 | 0.0199237 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54962541 | TGTACTTTTGGAAAA[C/T]GAGTTCTGTCCTACA | 11169 |
rs142579153 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | WDHD1 | GRCh38.p7 | 14:54956592 | GCAGTGAGCTGAGAT[C/T]CTGACACTGCACTCC | 11169 |
rs142608530 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002547 | AAAAATAAAGGTGAT[A/C/G]ACTCTATTGCTTGCA | 11169 |
rs142746313 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013326 | CACCCCATCTCAAAA[A/C]AAAATGGTAGGGCAA | 11169 |
rs142778442 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54970192 | GAGTACTGAAAATCT[C/T]AGCCAGAACAATCAA | 11169 |
rs142787454 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009037 | CCCGACCTTGTGATC[C/T]GCCCACCTCAGCCTC | 11169 |
rs142808549 | in-del | -/C | 0.265453 | 0.249522 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002618 | TGATTACTTTTTTTT[-/C]CCCCCAAGAGACAGT | 11169 |
rs142885861 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54972829 | CCTAATATAGGTTAA[A/G]TGTTTATTAGATATT | 11169 |
rs142890334 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949394 | ATCAACTGGAAGAAA[G/T]GGTATCAGTGATCAA | 11169 |
rs142895485 | snp | A/G | 0.0111196 | 0.0737302 | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938815 | ATAATTAAATACAAT[A/G]CATGATTCTCGATTG | 11169 |
rs142899671 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015848 | GGACTGCAGGCGTGC[A/G]CCACCACACCCAGCT | 11169 |
rs142915719 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975903 | TGAACAAAAAGAAAG[C/T]ATAAATACCACTGAG | 11169 |
rs142923458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55012127 | TGGGGAAAAAAAATC[C/T]AATTTTAAAATTTGC | 11169 |
rs142925385 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969189 | GACTACAGGTGCCCA[C/G]CACCACGCCCAGCTA | 11169 |
rs142934930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014006 | AGACATTAGCCAGTA[C/T]TTTTTCTCATTTTAT | 11169 |
rs142951018 | in-del | -/GATCGCTTG | 0.135484 | 0.22223 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959309 | AGGCTGAGGTGGAAA[-/GATCGCTTG]GGTCTGGGGGGTTGA | 11169 |
rs143007021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54992444 | GCAGTGAACCGAGAT[C/T]GTGCCACTGCACTCT | 11169 |
rs143016162 | snp | C/T | 0.000133324 | 0.0081636 | missense | WDHD1 | GRCh38.p7 | 14:54957038 | TGAAACAGTACCTGC[C/T]TAGGCTTCGGCTTTG | 11169 |
rs143017424 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949000 | CCAAAACCCCATGTG[C/T]ACGTCACCATCATCA | 11169 |
rs143022988 | in-del | -/AAC | 0.463881 | 0.12944 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966340 | CTCCGTCGCACAAAA[-/AAC]AACAACAACAACAAC | 11169 |
rs143038306 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987740 | TTCTCCTGTCTCTTG[C/T]CTCAGCCTCCCGAGT | 11169 |
rs143101734 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939836 | GGCACAAAAGAAATC[A/G]CGGTTTTTGCCACTG | 11169 |
rs143128283 | snp | G/T | 0.0429648 | 0.14013 | intron-variant | WDHD1 | GRCh38.p7 | 14:54980300 | CTGTGCTCCAGCCTG[G/T]GTGACAGAGTGAGAC | 11169 |
rs143148619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015622 | GGAATGGATTCAGAT[A/G]TAAGACCCTAGGGAT | 11169 |
rs143168095 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | WDHD1 | GRCh38.p7 | 14:54956836 | CTCAAGTGATCCTCC[C/T]ACCTCAGCCTCCTGA | 11169 |
rs143189065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025469 | CCACCTTACGAGAAA[C/T]ACCCACAAGTGTGGA | 11169 |
rs143191961 | snp | A/G/T | 0.00796202 | 0.0626708 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024547 | ATCACACTTACCCAA[A/G/T]CTTGTGGGGAAAAGC | 11169 |
rs143267073 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995050 | CAGTTGACGCGATCT[C/T]GGCTCACTGCAACCT | 11169 |
rs143362150 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989947 | GGGATTATAGGCGTG[A/G]GCCATCACGCCCGGC | 11169 |
rs143362180 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028779 | ATGGTAAAAGCTTGA[A/G]CCTCCGAGTTTAACA | 11169 |
rs143372995 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999427 | TTAAATCACCTCTCC[G/T]GTTTTCAGCCCCACT | 11169 |
rs143428228 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008249 | TTAATTTGGCCCAGT[A/G]ATACGACATATAACA | 11169 |
rs143439628 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022046 | TCTAGAGGTTGAATT[C/T]GAGACATTGTGTTTG | 11169 |
rs143443929 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007608 | TGCAGAATAAACAAA[C/T]GATATACTCATTGAA | 11169 |
rs143448948 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | WDHD1 | GRCh38.p7 | 14:54951563 | CACAGCCAAATTCTA[C/T]CAGAGGTACAAGGAG | 11169 |
rs143474618 | in-del | -/C | 0.0414363 | 0.137845 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961157 | CATGCTATACCTCTG[-/C]TTAAAACCTACAACA | 11169 |
rs143476153 | snp | A/C/T | 4.02158e-05 | 0.00448403 | synonymous-codon, missense | WDHD1 | GRCh38.p7 | 14:54966604 | TGAACGCCAAAATTG[A/C/T]TCCTATAAAAGCAAA | 11169 |
rs143533126 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54954158 | AGGCATGGTGGCGTA[C/T]GCCTGCAATCCCAGC | 11169 |
rs143551122 | snp | G/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55012441 | TTTCTCCAAGTAACC[G/T]ACATCTCATTCCCAT | 11169 |
rs143562408 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954432 | TACAACATCAATGCA[A/G]AACAATCTGGCATTG | 11169 |
rs143588341 | in-del | -/T | 0.0644693 | 0.167566 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003836 | CCCAAAGTGCTGGGA[-/T]TATAGGCGTGAGCCA | 11169 |
rs143591181 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975648 | GCCACTGCACCCAAC[C/G]TCATATTCATAATTA | 11169 |
rs143654790 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953054 | CAATACCATTCAGGA[C/T]ATAGGAATGTGCAAG | 11169 |
rs143721890 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945028 | CAACCATGAACTCTG[C/T]ACTTTCAACTTTTTA | 11169 |
rs143728227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946372 | GACATTTCTGATTAA[A/G]TATATCAACATCTGT | 11169 |
rs143750335 | snp | A/G | 0.079617 | 0.182947 | intron-variant | WDHD1 | GRCh38.p7 | 14:54980651 | TCTACTAAAAATACA[A/G]AAATTAGCTGGGCAT | 11169 |
rs143759248 | snp | A/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941352 | CACCAATATAATTAC[A/T]ACATTATCTTATAAA | 11169 |
rs143779072 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005756 | TCCTTCTCTGGGTAG[G/T]GCAGAAAGCCCTCAT | 11169 |
rs143841239 | snp | A/C | 0.0807149 | 0.183963 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961912 | CACGATCTCGGCTCA[A/C]TGCTACCTCCACCTC | 11169 |
rs143942035 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54970488 | CAAGAACTACAAAAC[A/G]CTGTTGAAAGAAATC | 11169 |
rs143954638 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993065 | GTTACAAAATTAAAC[A/T]TGATTTTAAAAAATC | 11169 |
rs143976463 | snp | C/T | 0.0027628 | 0.0370643 | missense, intron-variant | WDHD1 | GRCh38.p7 | 14:54995765 | CAGCATTACTCATAT[C/T]ATCTCCATCAAAAAG | 11169 |
rs143991883 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994381 | TGCCATACAGACATA[C/T]AATGTGAGTTACAGC | 11169 |
rs144085983 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026553 | ACTACCATGACGGCC[C/T]GAATCAAACAATAAT | 11169 |
rs144086520 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955156 | TTTGCACATAAATAG[A/G]ATAATTTTGGAAAGT | 11169 |
rs144095527 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963669 | GCCAGGCGTGGTGGC[A/G]TGCGCCTGTAATCCC | 11169 |
rs144151656 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54945925 | AAAGTCTAAACTTTT[-/T]AAGGTTAAAAAAATT | 11169 |
rs144169472 | in-del | -/CTGC | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54963890 | GCCAAGGCAGAGGGA[-/CTGC]TAGAGGCCAGGAGTT | 11169 |
rs144187979 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948272 | ACCTCACCCGGGAAG[C/T]GCAAGGGGTCAGAAA | 11169 |
rs144212862 | snp | C/T | 1.65119e-05 | 0.00287327 | WDHD1 | 14 | allele_origin=T(somatic)/C(germline) | 14:54984802 | CAAAATTTGTTTTTT[C/T]TTTTTCCCCAGCTCT | 11169 |
rs144213385 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009767 | TTCCATCAAGCTATG[C/T]TTTCAGTATTATAAA | 11169 |
rs144222477 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949407 | AAGGGTATCAGTGAT[C/G]AAAGATCAAATGAAT | 11169 |
rs144243246 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989714 | ACCCAAGCTGGAGTG[C/G]AGTGGCATGATCTCG | 11169 |
rs144271979 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006322 | AAAAGTTTCTTTATA[C/T]AGATCTTTCACATTT | 11169 |
rs144290065 | snp | C/T | 0.00107658 | 0.023176 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941488 | AGGGTCACTTTCTTC[C/T]TTTACTCCTGCTTAA | 11169 |
rs144355243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993211 | CAGCCTCGACCTCTC[A/G]GGCTCAAGAGATCCT | 11169 |
rs144372566 | in-del | -/G | 0.00835141 | 0.0640778 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55027591 | TCCGGTCTCTTTCTT[-/G]GGGCCCAGTTAGCAG | 11169 |
rs144374145 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963786 | GCCTGGGCGAGAAAG[C/T]GAGACTCTGTCTCAA | 11169 |
rs144414386 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006258 | TCCTTTCTAAGAATA[C/T]ATGTTTCTATTTATC | 11169 |
rs144414539 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961075 | CTCTCAAAATGCTGA[A/G]GTTACAGACATGAGC | 11169 |
rs144460957 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007044 | CCAGCCTGGGCAACA[C/T]GATGAAACCTCCTCT | 11169 |
rs144537572 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948126 | GCTCCCAGCATGAGC[A/G]ATGCAGAAGACGGGT | 11169 |
rs144561456 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943459 | GAGTACAGTGACACA[A/G]TCACGGCTCACTGCA | 11169 |
rs144589929 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54995361 | AATTTTATTGAATTT[G/T]GCTCTGTATTATTTC | 11169 |
rs144673163 | snp | C/G | 0.000301316 | 0.0122706 | missense | WDHD1 | GRCh38.p7 | 14:54963151 | CCACACAACGGAATT[C/G]TCGCTCCAGTTTACA | 11169 |
rs144685967 | snp | C/G | 0.0360663 | 0.129354 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952780 | ACCAAAACAGAGATA[C/G]AGACCAATGGAACAG | 11169 |
rs144697505 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55020416 | AAACACTTCATTTGG[C/T]TTCTAAACATCCTTC | 11169 |
rs144736483 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009580 | GGGATTATAGGCACC[C/T]GCTACTATGCCCAGC | 11169 |
rs144761497 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952177 | AAATAAAGGGTATTC[A/T]ATTAGGAAAAGAGGA | 11169 |
rs144772495 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964556 | AGGCAGGAGAATGGC[A/G]TGAACCTGGGAGGCG | 11169 |
rs144794579 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54956510 | GGGCGTGATGTCAGG[C/T]CTCTGTAATCCCAAC | 11169 |
rs144800098 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949197 | CTTCAGACGATCAAA[A/C]CTCTCCGAGCTAAAG | 11169 |
rs144827897 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982005 | TTTATTTATTTATTT[A/T]TTATTATTATTTTTT | 11169 |
rs144829586 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020899 | TATCAGGAAAATCAT[A/T]AAGAGGAGAAAAAAT | 11169 |
rs144917629 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021960 | ACTGGGGTTCTCTTC[C/T]ATAGCAATGACAATC | 11169 |
rs144949169 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011185 | CTCCTTTACAGTCTT[C/T]TTCATATACAAAGGC | 11169 |
rs145015087 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957539 | CATTTGGAAATATTT[A/C]TTTGTATACAAATGT | 11169 |
rs145036932 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026658 | ACATATAAAGTTTAA[A/G]GATAAATGTTTTAAC | 11169 |
rs145116045 | snp | A/C | 0.00183456 | 0.030231 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007405 | AAGAAAATTTCTTTC[A/C]TTTATGAAAATCCCC | 11169 |
rs145172441 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54985482 | GGTAATGAGAAACAA[C/T]GGTAAGAGATGAGGT | 11169 |
rs145221699 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942346 | GTATGAAATAATACA[A/G]AAAGATCCTGTGTAG | 11169 |
rs145381877 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946996 | TGCAGTGAGCTGAGA[C/T]TGCACCAGTGGACTC | 11169 |
rs145387488 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | WDHD1 | GRCh38.p7 | 14:54965985 | AAAAAAATTTTAACT[A/G]CAAGACCAACTAGAA | 11169 |
rs145429901 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988209 | CAAACGGGTGACTAG[C/T]ACATTTTTTGGTTTG | 11169 |
rs145460625 | snp | A/G | 4.94499e-05 | 0.00497217 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54987207 | CACCACAGGTCCAGC[A/G]AGGCTGAATACCTCT | 11169 |
rs145468141 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983444 | TCAGGAGGTCGAGGC[A/G]GGTGGATCACATGAG | 11169 |
rs145470195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022905 | TCTTGGCTCACTGCA[A/G]CCTCCACCTCCCGGG | 11169 |
rs145521075 | snp | C/G | 3.295e-05 | 0.00405881 | missense | WDHD1 | GRCh38.p7 | 14:54989085 | TCGTGGGAAAGATCT[C/G]CTATTGTATAATTCA | 11169 |
rs145557179 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948813 | GAGACGAGGCTTCCA[A/G]AGGAATGACCAGGCA | 11169 |
rs145588674 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994930 | CTCTATGTTAGTAAT[C/T]TGTGTCTTCTCTTTA | 11169 |
rs145612037 | snp | C/T | 3.29685e-05 | 0.00405995 | missense | WDHD1 | GRCh38.p7 | 14:54957150 | TATTGTCTAAAATAT[C/T]AGTTGAACGTGCTGA | 11169 |
rs145612447 | snp | C/T | 7.68315e-05 | 0.00619757 | missense | WDHD1 | GRCh38.p7 | 14:54966593 | TGAAATATAACTGAA[C/T]GCCAAAATTGCTCCT | 11169 |
rs145704044 | snp | G/T | 0.000153988 | 0.00877328 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54941667 | TTCACTTGCCGTTTC[G/T]CCTTTGGCTTTGTTA | 11169 |
rs145725165 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961538 | GTTCCCATGCACCTT[G/T]GCCTTGCTGACTGTT | 11169 |
rs145747032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014460 | CAATAAAATAGGGAC[C/T]GTATCTTCCTTGTCC | 11169 |
rs145757396 | in-del | -/G | 0.0659589 | 0.169201 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000201 | AGTTCTAAGAGTTAA[-/G]GCTAATTCAGAGTAG | 11169 |
rs145776597 | snp | C/T | 0.00795532 | 0.062565 | | | GRCh38.p7 | 14:55003877 | CTACCAACTGTATAT[C/T]TTTTATGTACACTGT | 11169 |
rs145782612 | snp | C/T | 0.0182019 | 0.0936463 | | | GRCh38.p7 | 14:54939524 | ATATTATTGATATGA[C/T]GATGATTAATAATTA | 11169 |
rs145785782 | snp | C/T | 0.0178098 | 0.0926698 | | | GRCh38.p7 | 14:55011748 | CTTATTGTAAACTTA[C/T]TTTCAACTTATTATA | 11169 |
rs145788043 | snp | C/G | 0.0111196 | 0.0737302 | | | GRCh38.p7 | 14:54947581 | GGTAAAAATGAAATT[C/G]TGACTGTTCTTTTCT | 11169 |
rs145804301 | in-del | -/A | 0.0729998 | 0.176553 | intron-variant | WDHD1 | GRCh38.p7 | 14:54968451 | TGCATCTAGGGAAAC[-/A]TAGATAAACGAGAAC | 11169 |
rs145816455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999893 | GTCACTGCAGCAGAG[C/T]TCAAAATTATTTTTA | 11169 |
rs145870677 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013860 | GCAAGTGAACCATGA[C/T]GGCACCACTGCACTC | 11169 |
rs145936318 | snp | A/G | 0.00103715 | 0.0227486 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000693 | TCAAGAAAAATATAA[A/G]TTGTACATTTCTTTA | 11169 |
rs145950468 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998656 | TCACTTTTAATCATT[G/T]TGTTTAACAGATCCT | 11169 |
rs145955022 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960108 | TTCTTTCTAACATCA[A/C]CATCACCACCCTAGC | 11169 |
rs146056988 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974752 | GAATCACTTGAACCC[A/G]GAAGGAGGAGGTTGC | 11169 |
rs146068437 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013346 | TGGTAGGGCAAGTTA[C/T]GGCATTATCATACAT | 11169 |
rs146199445 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998084 | AGGGCGTGGTGGTGG[A/G]TGCCTGTTATCCTAG | 11169 |
rs146300842 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54983613 | GGAAGGCAGAGGTTG[C/T]AGTAAGCTGAGATCG | 11169 |
rs146301318 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946464 | AACCAACTGATAGTA[C/T]GAAAAATTAAATTAT | 11169 |
rs146336173 | in-del | -/TTCTCTATACTTA | 0.0509478 | 0.151255 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025406 | GGTCCCCTTATTTCT[-/TTCTCTATACTTA]GTCTCTGTGTCTTTT | 11169 |
rs146339243 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55012841 | CTCATGGTCTCATTA[C/T]TTCTCAGTAGACCCC | 11169 |
rs146347868 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961476 | CTTTTGCAGCCTTCA[C/G]TTCACACATACTGTT | 11169 |
rs146417050 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958946 | AAATATCTGTCTTCA[C/T]GACATTCTACTCACC | 11169 |
rs146432218 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028081 | AATTTTTCTGCGTTT[C/T]TGTGATACCTTCCAG | 11169 |
rs146433723 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953812 | AAAGGATGAATTCAT[A/G]TCCTTTGTAGGGACA | 11169 |
rs146554328 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | WDHD1 | GRCh38.p7 | 14:54970266 | GACTATATTACTCTA[C/T]ACATAGAATTGCTAA | 11169 |
rs146625135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009784 | TTCAGTATTATAAAA[C/T]AGGCCATCTGCCCAT | 11169 |
rs146635564 | snp | C/G | 0.0437281 | 0.141251 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007159 | CTAGAACCTGGGAGG[C/G]AGAGGTTGCAGTGAG | 11169 |
rs146698591 | snp | A/G | 6.64993e-05 | 0.00576587 | missense, intron-variant | WDHD1 | GRCh38.p7 | 14:54995717 | CTTTTGAAAAAGAAG[A/G]GATCTCAACTGCATT | 11169 |
rs146745713 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025947 | CTTGTCCAAAGAAGC[C/T]TTCCCTGACTCCTTT | 11169 |
rs146747141 | snp | C/T | 0.0111846 | 0.0739407 | intron-variant | WDHD1 | GRCh38.p7 | 14:54956992 | CTGAAGACAAACAGA[C/T]CCCATGCTGCTTACT | 11169 |
rs146757102 | snp | A/G | 0.0729998 | 0.176553 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022511 | ACATGGCAAAACCCC[A/G]TCTCTACTAAAAATA | 11169 |
rs146758959 | snp | A/G/T | 0.00835141 | 0.0640778 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954241 | CAGTGAGCCAAGATC[A/G/T]TGCCAATGCACTCCA | 11169 |
rs146798135 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943082 | CAAGTATCTACGTTA[C/T]TAGGTGCCTGTGCTG | 11169 |
rs146869171 | snp | C/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939324 | ACTCACCCCAGGTTG[C/G]TGCACAGATATGAGA | 11169 |
rs146869364 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975836 | TGACACGCTCTCAAA[A/T]GAATTTTTAAAAATT | 11169 |
rs146881077 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971134 | CAGAATATAAAAATC[A/C]CAGAAGAAACCCTAG | 11169 |
rs146885158 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:55023885 | CATTTCTCTTGACTG[C/T]GGATGGTCTGGAAAT | 11169 |
rs146924753 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982289 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 11169 |
rs146924980 | snp | C/T | 0.000527391 | 0.0162301 | missense | WDHD1 | GRCh38.p7 | 14:54944346 | CCTTTCTTTCTTCAG[C/T]TGACAATACTCTAAA | 11169 |
rs146934585 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977483 | AGGTGGGAGGATCAC[C/T]CGAGGTTAGTTCAAG | 11169 |
rs146967733 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947339 | GCAAAAAGAAAAAAG[G/T]GTTAAGCGGAAAAAA | 11169 |
rs147029864 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954710 | TGATAGCCTTGCTAT[A/T]GTATAAAGAAGTTCT | 11169 |
rs147030245 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999191 | TCATTTCAACATTCA[A/T]GTATCTAATCTTTCA | 11169 |
rs147040383 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996408 | AGCTCAGGAGTTCGA[C/G]ACCAGCCTGGACAAC | 11169 |
rs147072401 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958562 | GCCCTCAGTGATCTC[C/T]ACATTGTCAAATCTG | 11169 |
rs147190449 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006102 | CTCCTGAGCTCAAGC[A/G]GTCCTCCTGCCTCAG | 11169 |
rs147191560 | snp | A/G | 0.000878156 | 0.0209358 | intron-variant | WDHD1 | GRCh38.p7 | 14:54941719 | CAGGAGTGAAAAGGA[A/G]AGATTTTTAGAAAAT | 11169 |
rs147199684 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002554 | AAGGTGATCACTCTA[C/T]TGCTTGCACCCAAAA | 11169 |
rs147206630 | snp | A/G | 1.70988e-05 | 0.00292389 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008378 | ATGCCTGCAGGAATA[A/G]ACAATACATTTCTCT | 11169 |
rs147208092 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945645 | TTCCAGGTTCAAGTG[A/G]TTCTCCTGCCTCAGC | 11169 |
rs147241661 | snp | A/G | 0.000357821 | 0.013371 | synonymous-codon, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55008349 | CACTCTGACAGATCC[A/G]TCACAACTAGCTGAT | 11169 |
rs147297127 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020676 | GGTATCAGCCAAAGA[G/T]GTAAAGGTGACCCTT | 11169 |
rs147297724 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953460 | TGGCAATCATTAAAA[C/T]GTCAGGAAACAACAG | 11169 |
rs147307160 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017017 | AGAAAATCGCCCGTA[A/T]TAATTCCAATAATAG | 11169 |
rs147315592 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955263 | TTTTTGTATCTTTTG[C/T]TATTTCTCCCCATTA | 11169 |
rs147328486 | snp | A/G | 1.6517e-05 | 0.00287372 | missense | WDHD1 | GRCh38.p7 | 14:54967368 | GGAAGGGTTGGGGGA[A/G]ACCGAGAACCTTTAC | 11169 |