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 |