SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs9767 | snp | A/C | 0 | 0 | utr-variant-3-prime, intron-variant | SOCS2 | GRCh38.p7 | 12:93575921 | CAGGTGCAACTCAAT[A/C]CCCGTTAATAAAAAC | 8835 |
rs471902 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93585731 | TGAGATCTTTCCTTT[G/T]GGCTTACACGAAGGA | 8835 |
rs477179 | snp | A/G | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93593363 | TTTTATGGTTAGAAA[A/G]GGAGGTGTTTTTTaa | 8835 |
rs493893 | snp | A/T | | | intron-variant, downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93577209 | TCCAGCCTTCTCATA[A/T]TTAGTCGCTTGCGAA | 8835 |
rs493917 | snp | A/G | | | intron-variant, downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93577202 | TTCTCATATTTAGTC[A/G]CTTGCGAACACTAAC | 8835 |
rs493928 | snp | A/G | | | intron-variant, downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93577194 | TTTAGTCGCTTGCGA[A/G]CACTAACTCAGAACT | 8835 |
rs493955 | snp | C/G | | | intron-variant, downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93577191 | AGTCGCTTGCGAACA[C/G]TAACTCAGAACTTTT | 8835 |
rs494888 | snp | C/T | 0 | 0 | intron-variant, downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93577078 | TAGAAAGGCAAAAGA[C/T]CTTTAAAGAAATTCC | 8835 |
rs553544 | snp | A/C | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93574516 | CCATTTTATGAACAC[A/C]AACGGCGAGCCAGTT | 8835 |
rs655049 | snp | A/T | | | upstream-variant-2KB, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93569552 | GTGCCCTTAATCATG[A/T]TTCGTTTTTTAGAAA | 8835 |
rs655051 | snp | A/T | | | upstream-variant-2KB, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93569551 | TGCCCTTAATCATGT[A/T]TCGTTTTTTAGAAAG | 8835 |
rs681174 | snp | C/T | 0 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93593361 | TTCTTAAACCTCCTT[C/T]TCTAACCATAAAAGC | 8835 |
rs768774 | snp | G/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93574229 | ttttttttttttttt[G/T]GGTGGGGGGCACACC | 8835 |
rs768775 | snp | C/T | 0.336702 | 0.234484 | intron-variant | SOCS2 | GRCh38.p7 | 12:93574421 | TCAGCCAGTGTGTCA[C/T]GCTGCAGATGTTCTT | 8835 |
rs865244 | snp | C/T | 0 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93587431 | tcacgcctgtaatcc[C/T]agcactttggtaggc | 8835 |
rs865496 | snp | G/T | 0 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93587485 | aggagatcgagacca[G/T]cctggccaacatggt | 8835 |
rs866162 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SOCS2 | GRCh38.p7 | 12:93587420 | ggcgcagtggctcac[A/G]cctgtaatcccagca | 8835 |
rs903170 | snp | G/T | 0 | 0 | intron-variant, downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93580792 | TTTATTTCTAGGTTG[G/T]GGCCATCAATTCTGT | 8835 |
rs930316 | snp | A/G | 0.341909 | 0.232492 | intron-variant, upstream-variant-2KB | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93573259 | GCAGAGCGCGGGAAG[A/G]GCTTCTTGGAAATAG | 8835 |
rs998616 | snp | G/T | 0.457853 | 0.138915 | intron-variant | SOCS2 | GRCh38.p7 | 12:93604224 | AAAAAACAAGAAAAA[G/T]AGTTTTTCTCACTGT | 8835 |
rs1053642 | snp | C/G | 0.0209421 | 0.100162 | utr-variant-3-prime, intron-variant | SOCS2 | GRCh38.p7 | 12:93576155 | AGTGTTTATTTACTG[C/G]TGTTACTATTTGATT | 8835 |
rs1178550 | snp | A/G | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93590548 | aggcctgtaatccca[A/G]cactttgggaggccg | 8835 |
rs1178551 | snp | A/G | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93590565 | actttgggaggccga[A/G]gtgggcggatcacga | 8835 |
rs1178552 | snp | A/G | 0 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93590674 | tggcgcatacctgta[A/G]tcccagctactccgg | 8835 |
rs1316739 | snp | C/T | 0.409552 | 0.192466 | intron-variant | SOCS2 | GRCh38.p7 | 12:93574480 | TCTTTTTTAAAAAAT[C/T]AACTTTCTGAAGCTC | 8835 |
rs1316740 | snp | G/T | 0.336702 | 0.234484 | intron-variant | SOCS2 | GRCh38.p7 | 12:93574512 | TTTATGAACACAAAC[G/T]GCGAGCCAGTTTTCT | 8835 |
rs1389499 | snp | A/G | 0 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93574167 | ACAGCCTTCTATGTA[A/G]AAAGCACTGCTATGT | 8835 |
rs1498706 | snp | A/G | 0.412082 | 0.190341 | intron-variant | SOCS2 | GRCh38.p7 | 12:93603204 | TTAGCTTCACAGACC[A/G]TCCTGTGGCAACAAC | 8835 |
rs1498707 | snp | A/G | 0.391954 | 0.205789 | intron-variant | SOCS2 | GRCh38.p7 | 12:93603352 | TCCCTATTTTTTTAG[A/G]TGGGAAAAAGAAGAC | 8835 |
rs1498708 | snp | A/G | 0.365024 | 0.221967 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93570188 | CTTACCTGCGCGCCC[A/G]GAAGGGGCTTGGTGA | 8835 |
rs1553126 | snp | C/T | 0.146985 | 0.227789 | intron-variant | SOCS2 | GRCh38.p7 | 12:93605781 | CCTTCCTAATTTTAT[C/T]CTGTCTGACACTCTT | 8835 |
rs1802151 | snp | A/G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | SOCS2 | GRCh38.p7 | 12:93575443 | AATAAAATGTCGCAT[A/G/T]TAAAGGCTGAAGTCG | 8835 |
rs1802152 | snp | C/T | | | utr-variant-3-prime, intron-variant | SOCS2 | GRCh38.p7 | 12:93575483 | AGAATGCCTTGCCTT[C/T]TTAGGTTCTTTTCCA | 8835 |
rs1960033 | snp | G/T | 0.464416 | 0.128553 | intron-variant | SOCS2 | GRCh38.p7 | 12:93618156 | GCGGAAGGCAAAGGG[G/T]AAGCAGGCACATCTT | 8835 |
rs2053196 | snp | C/T | 0.341235 | 0.232758 | upstream-variant-2KB, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93569183 | CCTCCCCGCCCTCCG[C/T]CAGTTTTAGGAATAA | 8835 |
rs2055304 | snp | A/T | 0.256897 | 0.249905 | intron-variant | SOCS2 | GRCh38.p7 | 12:93617255 | AGCAGATTGCTAAAA[A/T]TCCCACCCTGGGATG | 8835 |
rs2055305 | snp | A/G | 0.253544 | 0.249975 | intron-variant | SOCS2 | GRCh38.p7 | 12:93617183 | CTGTTCCTGCTTATT[A/G]CACCTGGTAATGAAG | 8835 |
rs2072593 | snp | C/T | 0.336474 | 0.234568 | utr-variant-3-prime, intron-variant | SOCS2 | GRCh38.p7 | 12:93576250 | ACACTTTCATGGTAA[C/T]AGAGGATTGCCATAA | 8835 |
rs2200160 | snp | A/G | 0.334642 | 0.235236 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93570097 | CAGGGCTGGGATTCG[A/G]AAGGATCTCGGCACC | 8835 |
rs2364229 | snp | C/G | | | intron-variant, upstream-variant-2KB | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93573093 | CTCCCCAAGGAAGCA[C/G]CTAGGAAGCGGGGTC | 8835 |
rs2364230 | snp | A/T | | | intron-variant, upstream-variant-2KB | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93573095 | CCCCAAGGAAGCAGC[A/T]AGGAAGCGGGGTCGA | 8835 |
rs2364231 | snp | G/T | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93574232 | tttttttttttttGG[G/T]GGGGGGCACACCAAC | 8835 |
rs2364232 | snp | A/C | 0.331874 | 0.236213 | intron-variant | SOCS2 | GRCh38.p7 | 12:93601051 | ctgcctcgacccctg[A/C]aagtgttgggattat | 8835 |
rs2364275 | snp | A/G | 0.298651 | 0.24522 | intron-variant | SOCS2 | GRCh38.p7 | 12:93623438 | ATTTTTTAATTTATT[A/G]TTATTATACTTTACG | 8835 |
rs3729654 | snp | A/C | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93574578 | TGAGCGAAAGTTTAC[A/C]GGGCCACCACAAATA | 8835 |
rs3741674 | snp | C/T | 0.472896 | 0.113214 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93583224 | AGAGCGAAGACAGCC[C/T]TCCAGATCCCTTGAT | 8835 |
rs3741676 | snp | C/G/T | 0.000758528 | 0.0194604 | missense, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93574737 | TCATTAACAGTCATA[C/G/T]TTCCCCAGTACCATC | 8835 |
rs3782415 | snp | A/G | 0.341909 | 0.232492 | intron-variant | SOCS2 | GRCh38.p7 | 12:93573979 | CAATCACAACCATCC[A/G]TCTCCCCTGCATTCT | 8835 |
rs3816997 | snp | G/T | 0.35809 | 0.225425 | intron-variant, downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93577010 | CAGAAAAATCAAACA[G/T]CCAACACTAAACAGG | 8835 |
rs3825198 | snp | A/T | 0.344815 | 0.231323 | intron-variant, downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93583689 | CTTGGACGTAATAAA[A/T]CCCATGGCCTGCCCA | 8835 |
rs3825199 | snp | C/T | 0.345704 | 0.230956 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93583178 | AAAGGGTTATGATGA[C/T]GATGATGATGGCTGG | 8835 |
rs3887021 | snp | C/T | 0.334412 | 0.235318 | intron-variant | SOCS2 | GRCh38.p7 | 12:93593038 | CCTACTCTCTGTCCC[C/T]TTATCCTGGTTTCCT | 8835 |
rs3887022 | snp | A/G | 0.1652 | 0.235179 | intron-variant | SOCS2 | GRCh38.p7 | 12:93593130 | CTGACACCAGATTGG[A/G]TGGCCAGTTCTAGGA | 8835 |
rs3952438 | snp | C/T | 0.046775 | 0.145601 | intron-variant | SOCS2 | GRCh38.p7 | 12:93602153 | GCTGGAGTGCAGTGG[C/T]GCGATCACAGCTGCC | 8835 |
rs4438087 | snp | C/T | 0 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93614482 | CTTCCTTCCTTCCTT[C/T]CCTTCCTTCCTTCCT | 8835 |
rs4628790 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | SOCS2 | GRCh38.p7 | 12:93618251 | agaaaagaggtttca[C/T]tggctcacagtcctg | 8835 |
rs4638412 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | SOCS2 | GRCh38.p7 | 12:93618461 | caaggatggacacag[G/T]gagccatggagaagg | 8835 |
rs4761734 | snp | A/G | 0.346368 | 0.23068 | intron-variant | SOCS2 | GRCh38.p7 | 12:93626073 | GCCTGGGTTTTAGAC[A/G]GTTCTGCCAAAGGTT | 8835 |
rs6538436 | snp | C/G | 0.0185938 | 0.0946107 | utr-variant-3-prime, intron-variant, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93586138 | actgacCATATTAAA[C/G]AGTTAGGGCTACTAA | 8835 |
rs6538437 | snp | A/T | 0.489665 | 0.0711382 | intron-variant | SOCS2 | GRCh38.p7 | 12:93595959 | AGCAAATAGAGGGCA[A/T]AAACAGTCATAATTT | 8835 |
rs6538438 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | SOCS2 | GRCh38.p7 | 12:93603115 | CTATGAGAGTAAACA[C/T]TGCCTCCTATTTTTA | 8835 |
rs6538439 | snp | C/T | 0 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93614362 | TATATAGCAATtttc[C/T]ttctttctttctttc | 8835 |
rs6538440 | snp | C/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93614420 | ctttctttctttctt[C/T]ctttctttcccttcc | 8835 |
rs6538441 | snp | C/T | 0.039522 | 0.134904 | intron-variant | SOCS2 | GRCh38.p7 | 12:93619106 | ggaaagctatcccca[C/T]cggtagaactgaagg | 8835 |
rs6538442 | snp | A/G | 0.039522 | 0.134904 | intron-variant | SOCS2 | GRCh38.p7 | 12:93619286 | ttatttcctggccaa[A/G]cccaactggaagcca | 8835 |
rs6538443 | snp | C/T | 0.25801 | 0.249872 | intron-variant | SOCS2 | GRCh38.p7 | 12:93620299 | TCTAATAGTCAATTC[C/T]ATGGCTGTACCAAAA | 8835 |
rs7131921 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SOCS2 | GRCh38.p7 | 12:93619236 | tgggtaagttgcccc[A/G]cttcttcctcctccc | 8835 |
rs7131954 | snp | A/G | 0.253264 | 0.249979 | intron-variant | SOCS2 | GRCh38.p7 | 12:93619332 | ttacacagtccatag[A/G]ggtcagactctgggg | 8835 |
rs7132051 | snp | A/G | 0.125874 | 0.217008 | intron-variant | SOCS2 | GRCh38.p7 | 12:93619360 | gggccccagaacagg[A/G]caggaagggtggggc | 8835 |
rs7132054 | snp | G/T | 0.252983 | 0.249982 | intron-variant | SOCS2 | GRCh38.p7 | 12:93619367 | agaacagggcaggaa[G/T]ggtggggcacagggc | 8835 |
rs7132059 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SOCS2 | GRCh38.p7 | 12:93619385 | tggggcacagggcag[A/G]atcggagcaaacaga | 8835 |
rs7132372 | snp | A/G | 0.258843 | 0.249844 | intron-variant | SOCS2 | GRCh38.p7 | 12:93619836 | GCCTGCCTAAATCCC[A/G]GTTAACTTCTGGTTC | 8835 |
rs7300268 | snp | A/C | 0.27008 | 0.249192 | intron-variant | SOCS2 | GRCh38.p7 | 12:93622966 | CTTAAAAAAGGAATC[A/C]ATTTTAGGTTCAAAG | 8835 |
rs7305728 | snp | A/G | 0.104149 | 0.203046 | intron-variant | SOCS2 | GRCh38.p7 | 12:93611426 | TATTTTTGTAGAGAC[A/G]GGGTTTCACCATGTT | 8835 |
rs7309860 | snp | C/T | 0.126219 | 0.217206 | intron-variant | SOCS2 | GRCh38.p7 | 12:93596113 | TGTGTAGGAGAATCC[C/T]TGGGATCAATAATAG | 8835 |
rs7310389 | snp | A/G | 0.418653 | 0.184544 | intron-variant | SOCS2 | GRCh38.p7 | 12:93582860 | TAGTACATTGGGGTG[A/G]GAGTGCTCAGAGGAG | 8835 |
rs7310512 | snp | C/T | 0.416545 | 0.186448 | intron-variant | SOCS2 | GRCh38.p7 | 12:93582927 | ACGTAGATTGTAGTA[C/T]AGATTTTACCTCTAT | 8835 |
rs7313659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93583072 | TGTTTTCTTTTAGCT[A/G]TGGATCTTTGAACAT | 8835 |
rs7487609 | snp | A/G | 0 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93574448 | TCTTTTGGTTCATTA[A/G]AAGAAAATCTTAAGA | 8835 |
rs7953508 | snp | C/T | 0.440609 | 0.161766 | intron-variant | SOCS2 | GRCh38.p7 | 12:93589778 | GTCTGGCACTTTTTC[C/T]AGGAGAAACACATGT | 8835 |
rs7954840 | snp | A/G | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93607627 | gcaaaattcacaggg[A/G]tgccaagcaaaattc | 8835 |
rs7956250 | snp | A/G | 0.0374533 | 0.13162 | missense, upstream-variant-2KB, nc-transcript-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93572917 | CCCTGCGGTGCCTTG[A/G]GCCCTCCGGGAATGG | 8835 |
rs7957632 | snp | C/T | 0.34659 | 0.230587 | intron-variant | SOCS2 | GRCh38.p7 | 12:93604545 | TTTAAGAAAAAAAAC[C/T]GTGGTGGGTATTTTA | 8835 |
rs7959620 | snp | A/C | 0.0867769 | 0.189363 | intron-variant, upstream-variant-2KB | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93573243 | TCAGGCCTGGCGGAG[A/C]GCAGAGCGCGGGAAG | 8835 |
rs7961325 | snp | C/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93614442 | ttcccttccttcctt[C/T]cttccttccttcctt | 8835 |
rs7965450 | snp | C/T | 0.203267 | 0.245593 | intron-variant | SOCS2 | GRCh38.p7 | 12:93613702 | GAATATAGTTAACAA[C/T]TGAGTACTCTGGCTT | 8835 |
rs7965980 | snp | C/T | 0.434831 | 0.168337 | intron-variant | SOCS2 | GRCh38.p7 | 12:93610083 | atctcccaacacagt[C/T]gcactgaggattaag | 8835 |
rs7971647 | snp | C/T | 0.438386 | 0.164349 | intron-variant | SOCS2 | GRCh38.p7 | 12:93590078 | CCAACACGATGAAAC[C/T]CCATCTCTACCAAAA | 8835 |
rs7972755 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | SOCS2 | GRCh38.p7 | 12:93590965 | CTTTTTCTTTAAACT[C/T]ACTGGCTTTTCCCTT | 8835 |
rs7973805 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | SOCS2 | GRCh38.p7 | 12:93617859 | tgccactagtaactc[C/T]ggcctggacaggagc | 8835 |
rs7976218 | snp | C/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93614416 | ctttctttctttctt[C/T]cttcctttctttccc | 8835 |
rs7977788 | snp | A/G | 0.418491 | 0.184691 | intron-variant | SOCS2 | GRCh38.p7 | 12:93588556 | GTAGCCTAAGGCAGC[A/G]ATGGGGAGAAGGAGG | 8835 |
rs7979312 | snp | A/C | 0.145305 | 0.227022 | intron-variant | SOCS2 | GRCh38.p7 | 12:93606924 | tcccaaaatgctgac[A/C]ttacaggcgtgagct | 8835 |
rs7980987 | snp | C/T | 0.437965 | 0.164831 | intron-variant | SOCS2 | GRCh38.p7 | 12:93610124 | atgaacttcagggaa[C/T]acgttcaaactatag | 8835 |
rs9634212 | snp | A/C | 0.311614 | 0.242289 | intron-variant | SOCS2 | GRCh38.p7 | 12:93599490 | tgagttataggattt[A/C]tttacatattccagg | 8835 |
rs9669442 | snp | C/T | 0.145978 | 0.227331 | intron-variant | SOCS2 | GRCh38.p7 | 12:93607693 | actattttaatgcaa[C/T]agttgaaacttcatg | 8835 |
rs10083107 | snp | A/T | 0.33693 | 0.2344 | intron-variant | SOCS2 | GRCh38.p7 | 12:93602259 | CCTGGCTAACTTTTT[A/T]AAAAATTTTTATTTT | 8835 |
rs10400450 | snp | G/T | 0.325563 | 0.238307 | intron-variant | SOCS2 | GRCh38.p7 | 12:93613906 | AAAAATAAAAAGAAA[G/T]TTAAAGCTGGTACCC | 8835 |
rs10400575 | snp | A/T | 0.315009 | 0.24256 | intron-variant | SOCS2 | GRCh38.p7 | 12:93614039 | GATTAGGAATCCACT[A/T]TACTTGGAATGGACT | 8835 |
rs10492321 | snp | A/T | 0.315758 | 0.241197 | downstream-variant-500B, intron-variant | SOCS2 | GRCh38.p7 | 12:93586312 | GTTTACTGTTTTGCT[A/T]AATTGGCTATATTTC | 8835 |
rs10551233 | in-del | -/TTCC | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93614359 | TTGTATATAGCAATT[-/TTCC]TTCTTTCTTTCTTTC | 8835 |
rs10594657 | in-del | -/CA | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93578683 | AGATTTGCATGCTCG[-/CA]CACACACACACACAC | 8835 |
rs10745656 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant, upstream-variant-2KB | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93571609 | CGGCAGCAGTCCGAG[A/G]GTGGAGGTGTCCCAG | 8835 |
rs10745657 | snp | A/G | 0.465996 | 0.12588 | intron-variant, utr-variant-3-prime | SOCS2 | GRCh38.p7 | 12:93579725 | ATAAAGGTAACAAGT[A/G]TTGTTAGAGTGGCCT | 8835 |
rs10777531 | snp | A/G | 0.489434 | 0.0719116 | intron-variant | SOCS2 | GRCh38.p7 | 12:93594608 | TATTATTTTCACTTT[A/G]TTTCTTTAGATATAA | 8835 |
rs10777532 | snp | C/G | 0.286303 | 0.24735 | intron-variant | SOCS2 | GRCh38.p7 | 12:93622562 | TCTTTTCCTTATAAA[C/G]GAAACCTTTAAAACA | 8835 |
rs10859533 | snp | C/T | 0.341909 | 0.232492 | intron-variant | SOCS2 | GRCh38.p7 | 12:93577534 | TTTTTTTTTTTTTTT[C/T]CCCCCGGGAGAGGAA | 8835 |
rs10859534 | snp | A/G | 0.335559 | 0.234904 | intron-variant | SOCS2 | GRCh38.p7 | 12:93581432 | TTTTTTTTTTTTAAT[A/G]TGTGTCAATCTTATA | 8835 |
rs10859535 | snp | A/G | 0.288127 | 0.247076 | utr-variant-3-prime, intron-variant, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93586116 | GGGAAACCCACGGGT[A/G]CAGAGGACTGACCAT | 8835 |
rs10859536 | snp | A/G | 0.155325 | 0.23138 | intron-variant | SOCS2 | GRCh38.p7 | 12:93595956 | AGTAGCAAATAGAGG[A/G]CAAAAACAGTCATAA | 8835 |
rs10859537 | snp | A/G | 0.136506 | 0.222754 | intron-variant | SOCS2 | GRCh38.p7 | 12:93607272 | AAGGAGAAAAAAGTA[A/G]CATTGAAACCAGCTT | 8835 |
rs10859538 | snp | C/T | 0.427423 | 0.176128 | intron-variant | SOCS2 | GRCh38.p7 | 12:93612195 | CTAAAAAAATTTCTC[C/T]GATCTGTCCATTTCC | 8835 |
rs10859539 | snp | A/G | 0.233235 | 0.249437 | intron-variant | SOCS2 | GRCh38.p7 | 12:93613824 | TCACTCCACACTGTA[A/G]TCAAAATCATAACAC | 8835 |
rs10859540 | snp | C/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93614412 | CTTTCTTTCTTTCTT[C/T]CTTTCTTCCTTTCTT | 8835 |
rs10859541 | snp | A/G | 0.463018 | 0.130857 | intron-variant | SOCS2 | GRCh38.p7 | 12:93616411 | GGAGACCCTGATACA[A/G]CCATGCCTGACCTCT | 8835 |
rs10859543 | snp | C/T | 0.295854 | 0.245759 | intron-variant | SOCS2 | GRCh38.p7 | 12:93623787 | TCAGCTCACTGCAAC[C/T]TCCGCCTCCCGAGCT | 8835 |
rs11107111 | snp | G/T | 0.461259 | 0.133677 | upstream-variant-2KB, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93568607 | TTTTAGTAAAGACGG[G/T]GTTTCACCATGTTGG | 8835 |
rs11107112 | snp | A/G | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93574623 | TTTTTTTCTTTTTTA[A/G]AGCTAAAAAAATTAT | 8835 |
rs11107113 | snp | A/G | 0 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93574663 | CTTGCTCTGTTCTAA[A/G]AATTCTTATAATAAC | 8835 |
rs11107114 | snp | A/G | 0.352721 | 0.227922 | intron-variant | SOCS2 | GRCh38.p7 | 12:93579151 | CCTGGGCGACTGCCC[A/G]CCCTCCCATCCTTAC | 8835 |
rs11107115 | snp | A/G | 0.331411 | 0.236373 | intron-variant | SOCS2 | GRCh38.p7 | 12:93579211 | TCATGGGCATAAGGG[A/G]TAGTTAATTCCTGCC | 8835 |
rs11107116 | snp | G/T | 0.281577 | 0.247998 | intron-variant | SOCS2 | GRCh38.p7 | 12:93584728 | TAATTATCCAGCTTG[G/T]AAGAGTCCCTGACAT | 8835 |
rs11107117 | snp | C/T | 0.282632 | 0.247861 | intron-variant | SOCS2 | GRCh38.p7 | 12:93585643 | TTTATAGAACATGTA[C/T]AGCCTCTTTAATTCC | 8835 |
rs11107119 | snp | A/T | 0.309154 | 0.242901 | intron-variant | SOCS2 | GRCh38.p7 | 12:93589356 | ATTCTGGGAATTTTT[A/T]TTTTAAATTCCCATG | 8835 |
rs11107120 | snp | C/T | 0.301681 | 0.2446 | intron-variant | SOCS2 | GRCh38.p7 | 12:93591706 | GGTCTCCCAGGACCT[C/T]ATGTAACCCAGCGTC | 8835 |
rs11107121 | snp | A/C/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93591820 | AGACGGCTGGGTGCA[A/C/T]TGTTTTTGCCGCATA | 8835 |
rs11107122 | snp | G/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93592941 | tttttttttttttGG[G/T]ATGTGTAATAATATC | 8835 |
rs11107123 | snp | A/G | 0.158962 | 0.232835 | intron-variant | SOCS2 | GRCh38.p7 | 12:93593282 | TCTGCTATGACTCCC[A/G]AATGCCTAAAGCTCT | 8835 |
rs11107124 | snp | C/G | 0.489434 | 0.0719116 | intron-variant | SOCS2 | GRCh38.p7 | 12:93594507 | TATTCTTTCTCAAAT[C/G]TGTCATTTAATTAAC | 8835 |
rs11107125 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | SOCS2 | GRCh38.p7 | 12:93599269 | AGCAATCCTCCTGCC[C/T]CAGCCTCCCAAGTGG | 8835 |
rs11107126 | snp | A/T | 0.416708 | 0.186302 | intron-variant | SOCS2 | GRCh38.p7 | 12:93603597 | AATCAAGTTAAATAA[A/T]CAAGAGATTATTACC | 8835 |
rs11107127 | snp | C/T | 0.313814 | 0.241719 | intron-variant | SOCS2 | GRCh38.p7 | 12:93612658 | AGGGAGGAATTGTAT[C/T]GTTTTTTTCCAATTG | 8835 |
rs11107128 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | SOCS2 | GRCh38.p7 | 12:93613513 | TAGTAGCTGCATACT[A/G]TCTCCGAGCCTTAGT | 8835 |
rs11107129 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | SOCS2 | GRCh38.p7 | 12:93614760 | gctggcattacaggc[A/G]cctgccaccatgcct | 8835 |
rs11107130 | snp | C/T | 0.253264 | 0.249979 | intron-variant | SOCS2 | GRCh38.p7 | 12:93616192 | AAggccaatcaaagc[C/T]agtgagacatgattt | 8835 |
rs11107131 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SOCS2 | GRCh38.p7 | 12:93619668 | GACCTTAGAGGTTAC[C/T]ATACCCTATTAAAGA | 8835 |
rs11107132 | snp | A/C | 0.0577344 | 0.159793 | intron-variant | SOCS2 | GRCh38.p7 | 12:93621614 | ccccagtacctggga[A/C]cacaagcacacacca | 8835 |
rs11107133 | snp | C/T | 0.348574 | 0.229746 | intron-variant | SOCS2 | GRCh38.p7 | 12:93624063 | GTCTTTAGGAGGTAA[C/T]TAAGTCATGAGAGTG | 8835 |
rs11107134 | snp | C/T | 0 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93624117 | CGCCTTGTAAAAGGT[C/T]TGGAGGAAACTAGTG | 8835 |
rs11107136 | snp | A/G | 0.089084 | 0.191327 | intron-variant | SOCS2 | GRCh38.p7 | 12:93625511 | tcagcactttgggag[A/G]cccaggcgagtggat | 8835 |
rs11305267 | in-del | -/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93583017 | TAACTCTGGGTTTTG[-/T]TTTTTTTTTTTTTTT | 8835 |
rs11306257 | in-del | -/T | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93599190 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGTCTCAC | 8835 |
rs11338219 | in-del | -/T | 0.436834 | 0.166111 | intron-variant | SOCS2 | GRCh38.p7 | 12:93588616 | TCTGGAGACAGTGAA[-/T]TTTTTTTTTTTTTTT | 8835 |
rs11353920 | in-del | -/T | 0.0310518 | 0.120672 | intron-variant | SOCS2 | GRCh38.p7 | 12:93598729 | TTCTTTATCTATTAA[-/T]TTACTTATTAGTAGA | 8835 |
rs11418330 | in-del | -/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93599172 | GTTGTGCTGTTTGTC[-/T]TTTTTTTTTTTTTTT | 8835 |
rs11611927 | snp | A/G | 0.349452 | 0.229367 | intron-variant, downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93583815 | ACACTTTACAAGTAT[A/G]ACCTCACTGAAAGTT | 8835 |
rs11615735 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | SOCS2 | GRCh38.p7 | 12:93618831 | CAAGGATGTTGTCTA[C/G]CTTGTTTATGGTTTG | 8835 |
rs11616183 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | SOCS2 | GRCh38.p7 | 12:93589092 | GCATGGTTTAAAACA[C/G]GGAAAACATCCATCC | 8835 |
rs11829153 | snp | G/T | 0.0372196 | 0.131242 | intron-variant | SOCS2 | GRCh38.p7 | 12:93610698 | ccatctcttttgcca[G/T]gtgaagacacagtgt | 8835 |
rs11830072 | snp | A/C | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93608943 | AAATACCTACTTTCC[A/C]GGGGTAAGTATTTAC | 8835 |
rs11831321 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93610748 | ccaccatgtaagaac[A/G]tggccataaggtgcc | 8835 |
rs11831953 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93611671 | ACTGTAATTATTGGC[A/G]GCCCCAGGAGTCATA | 8835 |
rs11832284 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | SOCS2 | GRCh38.p7 | 12:93617099 | GCAAACAATTATATC[A/C]CTGTGATATGCTAAG | 8835 |
rs11832523 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93612300 | TAGGTTGATTCCTCC[A/G]TGGTACTTTTCCATG | 8835 |
rs11832591 | snp | A/C | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93612565 | aagtgtactccctaa[A/C]gcaaactatgcattc | 8835 |
rs11832717 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | SOCS2 | GRCh38.p7 | 12:93605912 | ACTTCAGAtattaga[C/T]agggtatagtttcat | 8835 |
rs11834113 | snp | C/T | 0.17138 | 0.237316 | intron-variant, upstream-variant-2KB | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93572442 | CTGGGCGGGAAGACA[C/T]CCTGTTCACCCTCCT | 8835 |
rs11835183 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93609036 | aggctgaggcgggca[A/G]ataacttgagttcag | 8835 |
rs11836724 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | SOCS2 | GRCh38.p7 | 12:93611898 | ACAAAGGAGGCCTCC[A/G]TTGGTTTGCTTCTCT | 8835 |
rs11837265 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93612326 | CCATGGTATCATGCA[C/T]CTGTCCTTTGGAGCA | 8835 |
rs11837356 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93612645 | GTACTCCCAACATAG[A/G]GAGGAATTGTATTGT | 8835 |
rs12228514 | snp | C/T | 0.278133 | 0.248412 | intron-variant | SOCS2 | GRCh38.p7 | 12:93604786 | CTCCTCAGCCCCCAT[C/T]GTAGCTGGGATACAG | 8835 |
rs12228575 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SOCS2 | GRCh38.p7 | 12:93605023 | ATTTTTAGGAAATAA[A/G]CAGCCATGCCCACTC | 8835 |
rs12230050 | snp | A/G | 0.454784 | 0.1434 | intron-variant | SOCS2 | GRCh38.p7 | 12:93596777 | aggttgcagtgagcc[A/G]agattacaccactgc | 8835 |
rs12297997 | snp | A/G | 0.333722 | 0.235565 | intron-variant | SOCS2 | GRCh38.p7 | 12:93590125 | GGTGTGGTGGTGCGC[A/G]CCTATAATCTCAGCT | 8835 |
rs12298295 | snp | A/C | 0.333722 | 0.235565 | intron-variant | SOCS2 | GRCh38.p7 | 12:93590762 | GCACTCCAGCCTGGG[A/C]GACAGAGCAAGACTC | 8835 |
rs12300207 | snp | C/G | 0.0551013 | 0.156571 | intron-variant | SOCS2 | GRCh38.p7 | 12:93591690 | TCCGGGGCGCCGCTC[C/G]GGTCTCCCAGGACCT | 8835 |
rs12306938 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93570129 | GGCGTCAGCCCTGCA[C/G]GGAATGGCAGAGACA | 8835 |
rs12307020 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | SOCS2 | GRCh38.p7 | 12:93591416 | CGAGGAGAAAGCGTG[C/T]GTGCGTTCGTGTGTG | 8835 |
rs12309510 | snp | A/T | 0.0622301 | 0.165053 | intron-variant | SOCS2 | GRCh38.p7 | 12:93589361 | GGGAATTTTTTTTTT[A/T]AATTCCCATGGGTTC | 8835 |
rs12311225 | snp | A/T | 0.334182 | 0.235401 | intron-variant | SOCS2 | GRCh38.p7 | 12:93590062 | TTCGAGACCAGCCTG[A/T]CCAACACGATGAAAC | 8835 |
rs12312736 | snp | C/G | 0.387832 | 0.208572 | intron-variant | SOCS2 | GRCh38.p7 | 12:93603488 | ACTTCTCTTTCCCAC[C/G]TTTCCACATCCCATA | 8835 |
rs12313267 | snp | A/C | 0.191147 | 0.242974 | intron-variant | SOCS2 | GRCh38.p7 | 12:93591268 | AAACGAACAAACAAA[A/C]AAAAAAAAACAAGGC | 8835 |
rs12318214 | snp | A/G | 0.233818 | 0.249476 | intron-variant | SOCS2 | GRCh38.p7 | 12:93611906 | GGCCTCCGTTGGTTT[A/G]CTTCTCTGTTTTCTT | 8835 |
rs12319309 | snp | G/T | 0.123105 | 0.215401 | intron-variant | SOCS2 | GRCh38.p7 | 12:93608556 | CTGTAAAACTGAGGA[G/T]GATATTACATAGTTC | 8835 |
rs12320417 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | SOCS2 | GRCh38.p7 | 12:93624845 | ATTTCATACTAAAGA[C/T]AGAACCCTAAAACAA | 8835 |
rs12385812 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | SOCS2 | GRCh38.p7 | 12:93595414 | TTTCTACCCTTCTTT[A/G]TTGTTCTGATTTCAG | 8835 |
rs12426512 | snp | A/G | 0 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93581870 | ccattaccctgctta[A/G]ccattgcatttcatc | 8835 |
rs12427334 | snp | G/T | 0.364609 | 0.222182 | intron-variant | SOCS2 | GRCh38.p7 | 12:93625926 | TAACTGAGGTAGTGG[G/T]GATACTCTATCTTGT | 8835 |
rs12582500 | snp | A/G | 0 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93612287 | CTCTCCTGCAGTCTA[A/G]GTTGATTCCTCCATG | 8835 |
rs12582623 | snp | C/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93614400 | ctttctttctttctt[C/T]ctttctttctttctt | 8835 |
rs12813952 | snp | G/T | 0 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93593369 | GGTTAGAGAAGGAGG[G/T]TTAAGAAAAGCAAAC | 8835 |
rs12823940 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | SOCS2 | GRCh38.p7 | 12:93624930 | ATAGTGACTAATGCT[C/T]CTTCCTGTTCTTTCT | 8835 |
rs12824473 | snp | C/T | 0 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93614408 | CTTTCTTTCTTTCTT[C/T]CTTTCTTTCTTCCTT | 8835 |
rs13377612 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | SOCS2 | GRCh38.p7 | 12:93589982 | TTCCAggccgggtgt[A/G]gtggctcacgcctgt | 8835 |
rs13378027 | snp | A/G | 0.00914312 | 0.0669923 | upstream-variant-2KB, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93569106 | ggaggcggaggttgc[A/G]gtgagctgagatcac | 8835 |
rs17021316 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, intron-variant | SOCS2 | GRCh38.p7 | 12:93575408 | GGCTGACCAAGACCT[A/G]TTGATCCTTTTAGAT | 8835 |
rs17021320 | snp | A/G | 0.0356815 | 0.128715 | utr-variant-3-prime, intron-variant | SOCS2 | GRCh38.p7 | 12:93576431 | ATAATTTGAATAGGC[A/G]TAACACTGATGTCCT | 8835 |
rs17021323 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | SOCS2 | GRCh38.p7 | 12:93579094 | CTGTTTGATGATCTC[A/G]TTTCTACCTCCACCA | 8835 |
rs17021324 | snp | A/G | 0.0883596 | 0.190715 | intron-variant | SOCS2 | GRCh38.p7 | 12:93582072 | AAATGCATTGTTAAA[A/G]GCAGTGTAGTTACTT | 8835 |
rs17021325 | snp | C/T | 0.0980852 | 0.198549 | intron-variant | SOCS2 | GRCh38.p7 | 12:93582277 | GCTGTCTGAGGGTGA[C/T]TTGGGGCAGATCTTG | 8835 |
rs17021343 | snp | A/T | 0.348351 | 0.229841 | intron-variant | SOCS2 | GRCh38.p7 | 12:93584668 | AATAATGATGCTATT[A/T]TTGGGACTTTGATTT | 8835 |
rs17021352 | snp | C/T | 0.0770498 | 0.180522 | downstream-variant-500B, intron-variant | SOCS2 | GRCh38.p7 | 12:93586454 | AATTTTAATTTACTT[C/T]TGAGGAAAATTCTAT | 8835 |
rs17021354 | snp | A/G | 0.095934 | 0.196885 | intron-variant | SOCS2 | GRCh38.p7 | 12:93588520 | CATCACCAAAGGAAC[A/G]TGATCGTTGAGGAGG | 8835 |
rs17021379 | snp | A/G | 0.124837 | 0.216412 | intron-variant | SOCS2 | GRCh38.p7 | 12:93597944 | GTTTTAAAAATTCAC[A/G]TAAGTCAACAAATAT | 8835 |
rs17021383 | snp | A/C | 0.264906 | 0.249555 | intron-variant | SOCS2 | GRCh38.p7 | 12:93605007 | ACATGTATAGGGTAA[A/C]ATTTTTAGGAAATAA | 8835 |
rs17021389 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | SOCS2 | GRCh38.p7 | 12:93607533 | CTCTGCCTTTGGAAA[C/T]GTTAAAATTGAAGTC | 8835 |
rs17021394 | snp | C/T | 0.114387 | 0.210022 | intron-variant | SOCS2 | GRCh38.p7 | 12:93610926 | ATGGACTAAGACACA[C/T]TTTCACAATATCATA | 8835 |
rs17021407 | snp | C/T | 0.178785 | 0.239642 | intron-variant | SOCS2 | GRCh38.p7 | 12:93620032 | TGAAATATCTTGGAA[C/T]TGGAAATTTTTGTGT | 8835 |
rs17731257 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93583625 | GAGGTGCATCATTGA[A/G]CCTGGGTAATGGCTG | 8835 |
rs28446355 | snp | G/T | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93607750 | AAAATACGCTGTCAT[G/T]TGTTTGTTTTACCAT | 8835 |
rs28613781 | snp | A/G | 0.0279526 | 0.114869 | upstream-variant-2KB, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93569780 | AAGTTTGCAAGACGC[A/G]CCTCCCTCCCACCCC | 8835 |
rs28632060 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93607591 | AATAGGGTGAGGCAA[A/G]TGAGGCATTCACTCC | 8835 |
rs28690407 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | SOCS2 | GRCh38.p7 | 12:93607710 | GTTGAAACTTCATGA[C/T]GAGCAAATATCAATA | 8835 |
rs34035515 | snp | A/T | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93611120 | CAGGAGATGAACTTC[A/T]GGCCAGTTATTACCA | 8835 |
rs34144226 | in-del | -/C | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93615679 | ATCTCACTACAACCT[-/C]CCACCTCCTGGGTTC | 8835 |
rs34198600 | in-del | -/A | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93578116 | GATTGCTTTTTAGGG[-/A]ACTTGGAGATTTTTT | 8835 |
rs34418367 | in-del | -/C | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93594076 | AACTGACAGGAAGCA[-/C]CTGGGGGATTATGAT | 8835 |
rs34498070 | in-del | -/C | 0.144632 | 0.226711 | intron-variant | SOCS2 | GRCh38.p7 | 12:93607502 | GAAGAAGAACACAAG[-/C]ATACCTGCTGTAGCC | 8835 |
rs34674625 | snp | C/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93614540 | TTCCTTCCTTCCTTC[C/T]TTCTTTCTTTCTTTC | 8835 |
rs34822550 | in-del | -/G | | | intron-variant, downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93581089 | AAGAGAGAAAAGTAA[-/G]GGGAGATGGAGCATC | 8835 |
rs34870113 | in-del | -/G | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93573757 | ACAGGGGGAGGGAGA[-/G]GGGAAAAGTTCTCTC | 8835 |
rs34904787 | in-del | -/C | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93620922 | GATACCTTTGGGAAG[-/C]CCCACTCATTCATCT | 8835 |
rs35000205 | in-del | -/T | 0.434831 | 0.168337 | intron-variant | SOCS2 | GRCh38.p7 | 12:93595907 | TTAATTTGTTTTTAA[-/T]TTTTTTTTTATGTGA | 8835 |
rs35017212 | in-del | -/G | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93613122 | AGGGCAATGCCAAGG[-/G]AACAGAGGAAGCCAA | 8835 |
rs35110678 | in-del | -/G | | | intron-variant, downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93583842 | GTTCCCCACAAACAT[-/G]CTGAAGTAGATTCTG | 8835 |
rs35110908 | in-del | -/A | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93625146 | AATCATTCACTGACT[-/A]ATCTGGTCATCTCCT | 8835 |
rs35230804 | snp | A/G | 0.00716266 | 0.059414 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93569927 | GAAATTTTGGATCCG[A/G]TTTTCCCGTGATTGT | 8835 |
rs35259505 | in-del | -/T | 0.464309 | 0.12873 | intron-variant | SOCS2 | GRCh38.p7 | 12:93574603 | CGCTCACACACCACC[-/T]TTTTTTTTTTTCTTT | 8835 |
rs35305411 | in-del | -/A | | | intron-variant, utr-variant-3-prime | SOCS2 | GRCh38.p7 | 12:93580619 | GAGTGAGACTGTCTC[-/A]AAAAAAAAAAAAAAA | 8835 |
rs35358522 | in-del | -/G | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93606214 | GCAAGGAAAGCTGGG[-/G]AAATTTGGTCTTTGT | 8835 |
rs35377066 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93611061 | CATTTTATAAATCTT[C/T]AAGGAGGTGTCCTAG | 8835 |
rs35402510 | snp | G/T | 0.0540123 | 0.155206 | utr-variant-3-prime, intron-variant, missense | SOCS2 | GRCh38.p7 | 12:93575600 | GCCTCACTGCAATTT[G/T]ATATGCCTGCTGATC | 8835 |
rs35408505 | snp | C/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93614532 | TTCCTTCCTTCCTTC[C/T]TTCCTTCCTTCTTTC | 8835 |
rs35481542 | in-del | -/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93588615 | TCTGGAGACAGTGAA[-/T]TTTTTTTTTTTTTTT | 8835 |
rs35561293 | snp | C/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93614536 | TTCCTTCCTTCCTTC[C/T]TTCCTTCTTTCTTTC | 8835 |
rs35564612 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | SOCS2 | GRCh38.p7 | 12:93616246 | ATGTGCTCCATTGGG[G/T]TTGCTGAGAGGATGA | 8835 |
rs35572626 | in-del | -/ATTT | 0.419296 | 0.183954 | downstream-variant-500B, intron-variant | SOCS2 | GRCh38.p7 | 12:93586765 | ATATTTATTTCCTTC[-/ATTT]ATTTAGTTATTCATT | 8835 |
rs35617353 | in-del | -/A/AA | 0.487049 | 0.0794222 | intron-variant | SOCS2 | GRCh38.p7 | 12:93590783 | GCAAGACTCCGCCTC[-/A/AA]AAAAAAAAAAAAAAA | 8835 |
rs35660818 | in-del | -/A | | | intron-variant, utr-variant-3-prime | SOCS2 | GRCh38.p7 | 12:93580326 | ATCTTTAACATTCAG[-/A]AAAAATCCATGTTAG | 8835 |
rs35711257 | in-del | -/C | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93617367 | TGGAGAGGACAGGAG[-/C]AGGGGTTCCTGGAGT | 8835 |
rs35716264 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SOCS2 | GRCh38.p7 | 12:93614528 | TTCCTTCCTTCCTTC[C/T]TTCCTTCCTTCCTTC | 8835 |
rs35777498 | in-del | -/C | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93579147 | ATGCCTGGGCGACTG[-/C]CCCGCCCTCCCATCC | 8835 |
rs35977878 | in-del | -/A | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93625746 | GGGTGAGACCATCTC[-/A]AAAAAAAAAAAAAAA | 8835 |
rs36039977 | snp | G/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93585394 | TCAGAGGATCTCTTA[G/T]TGGTGTTTAAATGCC | 8835 |
rs36054681 | snp | G/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93614232 | CTAAGGCAGCCCTGG[G/T]GTTCAAACATATCCT | 8835 |
rs41343845 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SOCS2 | GRCh38.p7 | 12:93574478 | AAGAGCTTCAGAAAG[G/T]TGATTTTTTAAAAAA | 8835 |
rs41348344 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93567951 | TAACTTTAAAGCCAT[A/G]GTGCTAATGCATTCA | 8835 |
rs41350750 | snp | C/G | 0.0368353 | 0.130617 | intron-variant, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93571360 | AGAGAGAGTCCGAAC[C/G]GCGGCTCTGCCCCGC | 8835 |
rs41361945 | snp | C/T | 0.0349115 | 0.127424 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93570630 | AGGGCCAAGGATCGC[C/T]ATCCTTCCCTGAACC | 8835 |
rs41373351 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93568899 | GCCAGGAGGGGTGGC[C/T]CACGCCTGTAAACCC | 8835 |
rs41386246 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93571057 | CTCTTGCCAAGTCTC[A/G]TCGCAGCCGCCGCGG | 8835 |
rs41397344 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SOCS2 | GRCh38.p7 | 12:93574171 | AGCAGTGCTTTCTAC[A/G]TAGAAGGCTGTTCAT | 8835 |
rs41401047 | snp | A/G | | | utr-variant-3-prime, intron-variant | SOCS2 | GRCh38.p7 | 12:93576116 | TTTCTTCCAGATACA[A/G]GGGGATACCTGCCTG | 8835 |
rs41415544 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SOCS2 | GRCh38.p7 | 12:93573948 | GCCGGGGAGATGGTG[C/T]AGGCAGATGAAATCA | 8835 |
rs41417846 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | SOCS2 | GRCh38.p7 | 12:93573417 | CCGCGGGCCCCGCAG[A/G]CCCAGCAGCATCTGG | 8835 |
rs41442151 | snp | C/G | 0.00755907 | 0.0610114 | upstream-variant-2KB, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93568484 | GCAGTGGCACCGTCT[C/G]GGCTCACTGCAACCT | 8835 |
rs41442347 | snp | A/G | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93574299 | AATTACAGGAGTTGG[A/G]TTTTCCACTTTTTAA | 8835 |
rs41465448 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SOCS2 | GRCh38.p7 | 12:93573984 | GCAGGGGAGATGGAT[A/G]GTTGTGATTGGGTTT | 8835 |
rs41475949 | snp | A/G | 0.0209421 | 0.100162 | intron-variant, upstream-variant-2KB | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93571256 | AGGCTCCGCCCCGAG[A/G]AGAGTTACCGGGGAG | 8835 |
rs41477552 | snp | C/G | 0.0425523 | 0.139519 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93572726 | AGGGACTTTGTCATC[C/G]GTCCTCCAGGATCTG | 8835 |
rs41485845 | snp | A/G | 0.0670745 | 0.170406 | utr-variant-3-prime, intron-variant | SOCS2 | GRCh38.p7 | 12:93575422 | TGTTGATCCTTTTAG[A/G]TTAAAAATAAAATGT | 8835 |
rs41510744 | snp | C/G | 0.0205511 | 0.0992634 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93570449 | TGGGCACCGGGACGA[C/G]CACGGCGTCCCCACG | 8835 |
rs41513052 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93576855 | AGATTGCTAGGTGTG[C/T]CTCAGGAAGAGTTTA | 8835 |
rs41532546 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime, intron-variant | SOCS2 | GRCh38.p7 | 12:93576579 | TGCTATGTTAGTCTG[C/T]ATAACTGTTATAAAT | 8835 |
rs41534347 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93570393 | TCCCGCTCGCTGCCT[C/T]CCAGGACCTGATCAA | 8835 |
rs41535347 | snp | C/T | 0.00302023 | 0.0387426 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93571859 | CCCCCGCCCCATGTC[C/T]GCTGAGGAGGCTGCC | 8835 |
rs55673310 | snp | A/C | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93608875 | AGCTTAATTGGTGTT[A/C]CTTTAAGCAGGTCAC | 8835 |
rs55724094 | snp | A/C | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93592003 | AGGAGCTAGTTTTTC[A/C]ATTATTCTAAAAGTG | 8835 |
rs55755453 | snp | A/T | | | utr-variant-3-prime, intron-variant | SOCS2 | GRCh38.p7 | 12:93575657 | GCATTCTGATGTACC[A/T]AGGAGTTTTGTTAAA | 8835 |
rs55812332 | snp | A/G | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93612466 | TGTGAGGCTGGCCCA[A/G]GCTTCCTTTGAACCA | 8835 |
rs56210146 | snp | A/T | 0.135484 | 0.22223 | intron-variant | SOCS2 | GRCh38.p7 | 12:93618112 | TGTGTGGCACCTCCC[A/T]CTCTCTCTTCCGCCT | 8835 |
rs56380431 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SOCS2 | GRCh38.p7 | 12:93618572 | CATTCTCCCAACACC[A/G]CATGCCTGTCCTAGC | 8835 |
rs57366954 | in-del | -/CA/CACA/CACG | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93578712 | ACACACACACACACA[-/CA/CACA/CACG]GGCACACAACCCAGC | 8835 |
rs57409806 | snp | A/G | 0.356169 | 0.226336 | intron-variant | SOCS2 | GRCh38.p7 | 12:93624605 | ATGTGTTAATTACCA[A/G]TTCTTAGGTGTTTTG | 8835 |
rs57737887 | in-del | -/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93614428 | CTTTCTTCCTTTCTT[-/T]CCCTTCCTTCCTTCC | 8835 |
rs57865188 | in-del | -/A | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93624583 | TAAAAAAAAAAAAAA[-/A]TCTATTATGTGTTAA | 8835 |
rs58518753 | snp | C/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93614431 | TCTTCCTTTCTTTCC[C/T]TTCCTTCCTTCCTTC | 8835 |
rs58928339 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SOCS2 | GRCh38.p7 | 12:93592608 | CCCATGCATATTTCA[C/G]ATGGAAATAAATTCT | 8835 |
rs58939569 | snp | A/G | 0.349671 | 0.229272 | downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93626446 | AGAGCCTCTGAACAT[A/G]CTGTTCTCTTCCCAG | 8835 |
rs58998668 | snp | C/T | 0.121369 | 0.214369 | intron-variant | SOCS2 | GRCh38.p7 | 12:93614429 | TTTCTTCCTTTCTTT[C/T]CCTTCCTTCCTTCCT | 8835 |
rs59101373 | snp | C/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93601049 | TCCTGCCTCGACCCC[C/T]GAAAGTGTTGGGATT | 8835 |
rs59143989 | snp | C/G | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93601050 | CCTGCCTCGACCCCT[C/G]AAAGTGTTGGGATTA | 8835 |
rs59407384 | in-del | -/T | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93608019 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGCATCAT | 8835 |
rs59506224 | in-del | -/AA | 0.402762 | 0.197898 | intron-variant | SOCS2 | GRCh38.p7 | 12:93624569 | AGAGAGACTCCATCT[-/AA]AAAAAAAAAAAAATC | 8835 |
rs59716186 | snp | A/C | 0.0755793 | 0.179102 | intron-variant | SOCS2 | GRCh38.p7 | 12:93594739 | AAAGAATGTTATGTA[A/C]GGGAGTTTGTCAGGG | 8835 |
rs59730232 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SOCS2 | GRCh38.p7 | 12:93584724 | ATCCTAATTATCCAG[C/T]TTGGAAGAGTCCCTG | 8835 |
rs59850893 | in-del | -/TTTA | | | downstream-variant-500B, intron-variant | SOCS2 | GRCh38.p7 | 12:93586766 | TATTTCCTTCATTTA[-/TTTA]GTTATTCATTTTTTC | 8835 |
rs59883103 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93605649 | ATGTGAAATGACTAC[A/C]AGTGGATGCCTCCTG | 8835 |
rs60006837 | in-del | -/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93614097 | GCCATTTTTTTTTTT[-/T]CATTGATTCATTGAT | 8835 |
rs60299492 | snp | G/T | 0.283158 | 0.247791 | intron-variant | SOCS2 | GRCh38.p7 | 12:93609179 | GGCAAATCACCTGAG[G/T]TCAGGAGTTCGGGAC | 8835 |
rs60322788 | snp | C/T | 0.113334 | 0.209338 | intron-variant | SOCS2 | GRCh38.p7 | 12:93615243 | GAGAGCAAGGACTTT[C/T]TTTGGTTCATTGTTC | 8835 |
rs60484095 | snp | C/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93614487 | TTCCTTCCTTTCCTT[C/T]CTTCCTTCCTTCCTT | 8835 |
rs60655869 | snp | A/T | 0.356169 | 0.226336 | intron-variant | SOCS2 | GRCh38.p7 | 12:93624749 | TTGCTGGAACCCATT[A/T]AGTTGCTCCCATTAA | 8835 |
rs60733276 | in-del | -/C | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93614439 | CTTTCCCTTCCTTCC[-/C]TTCCTTCCTTCCTTC | 8835 |
rs60978319 | snp | C/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93614435 | CCTTTCTTTCCCTTC[C/T]TTCCTTCCTTCCTTC | 8835 |
rs61231395 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SOCS2 | GRCh38.p7 | 12:93586795 | TTTTTCAATCATTCA[C/T]TCACTCACTCATTCA | 8835 |
rs61244735 | snp | G/T | 0.35574 | 0.226537 | intron-variant | SOCS2 | GRCh38.p7 | 12:93624753 | TGGAACCCATTAAGT[G/T]GCTCCCATTAAGTTG | 8835 |
rs61297014 | in-del | -/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93614482 | CTTCCTTCCTTCCTT[-/T]CCTTCCTTCCTTCCT | 8835 |
rs61592237 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93622785 | TCTCACTCAGAAATC[A/C/G]CTCAAGCACACACAC | 8835 |
rs61661797 | in-del | -/T/TT | 0.625 | 0.125 | intron-variant | SOCS2 | GRCh38.p7 | 12:93601122 | CTTTTTTTTTTTTTT[-/T/TT]AAATATACCTTCTGT | 8835 |
rs61927247 | snp | A/G | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93598206 | GATTGATGAGAAGGA[A/G]GAGCAAGTGTTGATG | 8835 |
rs61927248 | snp | A/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93602112 | TGTTTGTTTTTTTAA[A/T]TACAAGGGCTTGCTG | 8835 |
rs61927249 | snp | A/T | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93614100 | ATTTTTTTTTTTTCA[A/T]TGATTCATTGATACA | 8835 |
rs61927250 | snp | A/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93614936 | TGTAGCAATTTTCTA[A/T]TTAAAAAAAAAAAAA | 8835 |
rs61927251 | snp | A/G | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93625689 | GGAGGCGGAGGTTGC[A/G]ATGAGCTGAGATCAC | 8835 |
rs61927252 | snp | A/C | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93626169 | TCTTTCTATTTATCC[A/C]ACAGATGCCGTTCTC | 8835 |
rs61934460 | snp | A/T | | | intron-variant, missense | SOCS2 | GRCh38.p7 | 12:93579464 | GCATTTTTTTTTTAA[A/T]TCTACTTATTTTTTA | 8835 |
rs61934461 | snp | G/T | 0.0221141 | 0.102801 | missense, intron-variant, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93585696 | CCAAAAGTTTTTCAG[G/T]TACTGCAAAACAGTG | 8835 |
rs61934462 | snp | A/T | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93588782 | CCACCAAGCCTAGCT[A/T]ATTTTTTTTTTTTAT | 8835 |
rs61936494 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93569579 | GCACACGGCTCCAGC[A/G]TTAACAAAGCTCTTT | 8835 |
rs67636036 | in-del | -/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93608001 | TTTGACTGTAAATCT[-/T]TTTTTTTTTTTTTTT | 8835 |
rs71071753 | in-del | -/T | 0.375 | 0.216506 | intron-variant | SOCS2 | GRCh38.p7 | 12:93590822 | CACTGGGAAGCTAAC[-/T]TTTTTTTTTTTTTTT | 8835 |
rs71071754 | in-del | -/A | 0 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93604978 | GTGAGCAATCAACTT[-/A]AAAAAAAAAAAAAAT | 8835 |
rs71071755 | in-del | -/A | 0 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93614473 | GGAAAGGAAGGAAGG[-/A]AAGGAAGGAAGGAAG | 8835 |
rs71433889 | in-del | -/A | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93599991 | CCAGTTTTAGCTTGT[-/A]CTTTTCACTGTTTAA | 8835 |
rs71458513 | snp | A/G | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93577495 | ATTTGTGAGTCAAGA[A/G]GCATTCCAGGAATAT | 8835 |
rs71458514 | snp | G/T | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93590012 | TAATCCCAGCACTTT[G/T]GGAGGCCAAGGTGAG | 8835 |
rs71458515 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93590029 | GAGGCCAAGGTGAGC[A/C/G]GATCATGAGGTCAGG | 8835 |
rs72138236 | in-del | -/TCTC | 0.356169 | 0.226336 | intron-variant | SOCS2 | GRCh38.p7 | 12:93625255 | GTCATACACACACAA[-/TCTC]TCTCTGTCATTAAAA | 8835 |
rs73218878 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SOCS2 | GRCh38.p7 | 12:93581641 | TTTTCCTTCTAGCTT[C/T]GTTCATTTATCTCAT | 8835 |
rs73218881 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SOCS2 | GRCh38.p7 | 12:93617827 | CTCTCCACTTCCACT[A/G]CCATCACTCTAGATC | 8835 |
rs73218883 | snp | A/G | 0.00953873 | 0.0683987 | downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93626579 | CCAAATAGCACCAGA[A/G]CTTTTCATCCACCAC | 8835 |
rs73371669 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SOCS2 | GRCh38.p7 | 12:93578990 | CTGGATTTCATGATG[C/T]CTTGATCCACATTAG | 8835 |
rs73371685 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SOCS2 | GRCh38.p7 | 12:93588100 | GGATTGGAAAAAAGC[A/G]TTATACTGTCATTTT | 8835 |
rs73373403 | snp | C/T | 0.100588 | 0.200439 | intron-variant | SOCS2 | GRCh38.p7 | 12:93597486 | ACACCCGCCTAATTT[C/T]TGTATTTTCAGTAGA | 8835 |
rs73373405 | snp | A/C/G | 0.118572 | 0.216062 | intron-variant | SOCS2 | GRCh38.p7 | 12:93598552 | AGAGGGATGGTGATA[A/C/G]CTTCTATTAAGATAG | 8835 |
rs73373407 | snp | G/T | 0.162253 | 0.234095 | intron-variant | SOCS2 | GRCh38.p7 | 12:93598648 | CTTATGTTGATACTT[G/T]TAGATAAAGTTAACT | 8835 |
rs73373410 | snp | C/T | 0 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93600299 | CAAGTTTTCCATAAG[C/T]ATGGGTCTGTTTATG | 8835 |
rs73373413 | snp | C/G | 0.183568 | 0.241012 | intron-variant | SOCS2 | GRCh38.p7 | 12:93600877 | CACTGACGACTTAAC[C/G]TCCTGGGCTCAAGGG | 8835 |
rs73373419 | snp | A/T | 0.100944 | 0.200705 | intron-variant | SOCS2 | GRCh38.p7 | 12:93602325 | GTTCTCGAACTCCTG[A/T]GGTCAAACAATCCTC | 8835 |
rs73373436 | snp | A/G | 0.0766824 | 0.180169 | intron-variant | SOCS2 | GRCh38.p7 | 12:93605433 | TGGATGAGGCCAGGG[A/G]CTTCAACCATACCTG | 8835 |
rs73373443 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | SOCS2 | GRCh38.p7 | 12:93612434 | CACTGAAAGGTCATT[C/T]CATATTTACAACTCC | 8835 |
rs73373452 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SOCS2 | GRCh38.p7 | 12:93617217 | TTGTGGGCCTGTTCC[C/T]GGTGGGAATCCCATA | 8835 |
rs73373473 | snp | A/G | 0.344815 | 0.231323 | intron-variant | SOCS2 | GRCh38.p7 | 12:93624299 | CATTTCTGGCCAAGC[A/G]CAGTGGCTCACGCCT | 8835 |
rs73373476 | snp | C/G | 0.348574 | 0.229746 | intron-variant | SOCS2 | GRCh38.p7 | 12:93624491 | GCAGGAGAATCACTT[C/G]AATCCGGGAGGCGGA | 8835 |
rs74320722 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SOCS2 | GRCh38.p7 | 12:93604919 | TCCTGCCTTGGCCCC[C/T]GCAAAGTGCTAGGAT | 8835 |
rs74344438 | snp | A/T | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93618114 | TGTGGCACCTCCCAC[A/T]CTCTCTTCCGCCTGC | 8835 |
rs74378528 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SOCS2 | GRCh38.p7 | 12:93595008 | GCCTTGACTTCCTTA[C/T]GTTTGTAAACTATGT | 8835 |
rs74452572 | snp | G/T | 0 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93597346 | ATCCCTTTTTTTTTT[G/T]AGACACAGTCTTGCT | 8835 |
rs74533887 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | SOCS2 | GRCh38.p7 | 12:93605805 | CACTCTTCTGAGGGG[C/T]AGTAGAGGCAGAATT | 8835 |
rs74540030 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93610193 | TATGTTACAACAGTC[A/G]TTCTCAGACTTTAGC | 8835 |
rs74624251 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SOCS2 | GRCh38.p7 | 12:93595595 | AAATCTGCTTTCATT[C/T]GTGTTAAATTCAGTT | 8835 |
rs74633924 | snp | A/C | 0 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93587681 | GCGAGACTCTGTCTA[A/C]AAAAAAAAAAAAAAA | 8835 |
rs74690012 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | SOCS2 | GRCh38.p7 | 12:93622444 | TGACATCATTGGCAT[A/G]TCAGCTATGATGCTG | 8835 |
rs74704855 | snp | A/G | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93603439 | GCCCAGTCCAAGTTA[A/G]TACAGCCTAAGGCTA | 8835 |
rs74774845 | snp | G/T | 0.0333695 | 0.124785 | intron-variant | SOCS2 | GRCh38.p7 | 12:93577689 | TACCTTAATTAGCAC[G/T]GTGCTCTGTGGGATT | 8835 |
rs74783531 | snp | A/G | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93618102 | TTGTTCAAAGTGTGT[A/G]GCACCTCCCACTCTC | 8835 |
rs74798206 | snp | A/G | 0 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93614954 | AAAAAAAAAAAAAAA[A/G]GACAGACTGATAAGG | 8835 |
rs74849107 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SOCS2 | GRCh38.p7 | 12:93597139 | AACCAGAAAACTGAT[C/T]TTGGTATAAAGTGTT | 8835 |
rs74894012 | snp | A/G | 0.112631 | 0.208878 | intron-variant | SOCS2 | GRCh38.p7 | 12:93606385 | GTTACCCCATTCAAC[A/G]CATCAGAAAAAGACT | 8835 |
rs74913774 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | SOCS2 | GRCh38.p7 | 12:93598026 | GCAAATCTTTTGTTC[C/T]AAATATGTAAACATT | 8835 |
rs74957550 | snp | A/T | 0.0770498 | 0.180522 | downstream-variant-500B, intron-variant | SOCS2 | GRCh38.p7 | 12:93586727 | AGATTGAAACTTTGC[A/T]TTATCTTTAACTTCT | 8835 |
rs75014064 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | SOCS2 | GRCh38.p7 | 12:93606337 | AAGTGGATAGTTTCT[A/G]TTAATCCTTCTGACA | 8835 |
rs75019459 | snp | G/T | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93618121 | CCTCCCACTCTCTCT[G/T]CCGCCTGCTCTGGCC | 8835 |
rs75092743 | snp | A/G | | | intron-variant, downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93580641 | AAAAAAAAAAAAAAA[A/G]AAAAGGAAAAGAAAA | 8835 |
rs75096142 | in-del | -/AA | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93614953 | TAAAAAAAAAAAAAA[-/AA]GACAGACTGATAAGG | 8835 |
rs75243398 | snp | A/T | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93588784 | ACCAAGCCTAGCTAA[A/T]TTTTTTTTTTTATTT | 8835 |
rs75327005 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93583095 | TTGAACATTACCCTA[C/T]GATCGAAGAGTTTTG | 8835 |
rs75328205 | snp | C/T | 0.126909 | 0.217598 | intron-variant | SOCS2 | GRCh38.p7 | 12:93614446 | CTTCCTTCCTTCCTT[C/T]CTTCCTTCCTTCCTT | 8835 |
rs75392263 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SOCS2 | GRCh38.p7 | 12:93626057 | ACGGCAAATCCTCAG[C/T]GCCTGGGTTTTAGAC | 8835 |
rs75459522 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | SOCS2 | GRCh38.p7 | 12:93618415 | CCACCCAAGCCCTTC[A/G]AAGACTTCCTGACAC | 8835 |
rs75479525 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93594620 | TTTGTTTCTTTAGAT[A/G]TAATTCTTGTTTTTC | 8835 |
rs75487859 | snp | A/C | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93618105 | TTCAAAGTGTGTGGC[A/C]CCTCCCACTCTCTCT | 8835 |
rs75526051 | snp | A/C | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93618092 | TGAGATCTGGTTGTT[A/C]AAAGTGTGTGGCACC | 8835 |
rs75549309 | snp | G/T | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93623723 | TGAATTTTTTTTTTT[G/T]TGAGACAGGGTCTCG | 8835 |
rs75588136 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | SOCS2 | GRCh38.p7 | 12:93592389 | TGAATCAGTCTCCTG[C/T]TAGTGGATATACAGG | 8835 |
rs75719693 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | SOCS2 | GRCh38.p7 | 12:93587277 | AATAAGATAATGGCT[A/G/T]CAACGGAGGTCTCTG | 8835 |
rs75752997 | snp | A/G | 0.0232847 | 0.105357 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93572201 | GGTTGGTGCCTCGGG[A/G]CCCCGCAGCGCTTTA | 8835 |
rs75770028 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | SOCS2 | GRCh38.p7 | 12:93626037 | TGGGACCCAAGGTGG[A/C]CACCACGGCAAATCC | 8835 |
rs75770268 | snp | G/T | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93623725 | AATTTTTTTTTTTTT[G/T]AGACAGGGTCTCGCT | 8835 |
rs75775132 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SOCS2 | GRCh38.p7 | 12:93581851 | TTAAACAGTCTAATA[C/T]ATCCCATTACCCTGC | 8835 |
rs75820776 | snp | C/T | 0.0236746 | 0.106192 | intron-variant, utr-variant-3-prime | SOCS2 | GRCh38.p7 | 12:93580141 | GGGGTGAGACTTTTT[C/T]GCCAGTTAAACCATC | 8835 |
rs75853284 | snp | A/G | 0.114387 | 0.210022 | intron-variant | SOCS2 | GRCh38.p7 | 12:93610469 | CCAAGTGCTGCAGGG[A/G]TGTCTGAGACCACAG | 8835 |
rs75903233 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | SOCS2 | GRCh38.p7 | 12:93590434 | TTGAGTCTGATTGCT[C/G]TTTACTGTTCTAACA | 8835 |
rs75912318 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | SOCS2 | GRCh38.p7 | 12:93611649 | TTAAAAAATTCTCTT[C/T]CATTACACTGTAATT | 8835 |
rs76072633 | snp | A/C | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93591278 | ACAAAAAAAAAAAAA[A/C]AAGGCTCAGCCCGAG | 8835 |
rs76074719 | snp | G/T | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93574231 | TTTTTTTTTTTTTTG[G/T]TGGGGGGCACACCAA | 8835 |
rs76100459 | snp | A/G | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93618239 | CTGTACAGCCTGCAG[A/G]ACTGTGAGCCAATGA | 8835 |
rs76160383 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SOCS2 | GRCh38.p7 | 12:93602254 | CTCCACCTGGCTAAC[C/T]TTTTTAAAAATTTTT | 8835 |
rs76197034 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | SOCS2 | GRCh38.p7 | 12:93606553 | TCCTTGGGATTACCA[C/T]ACCTCATCAGTGTTT | 8835 |
rs76227400 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SOCS2 | GRCh38.p7 | 12:93611562 | GTTTGCTTTGCAGAC[A/G]GCATTATTTCAACAA | 8835 |
rs76279988 | snp | A/G | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93618017 | TTGGATCATGGGGGC[A/G]GTTTCTCATGAATGA | 8835 |
rs76327742 | snp | A/T | 0.0295035 | 0.117819 | intron-variant, utr-variant-3-prime | SOCS2 | GRCh38.p7 | 12:93579512 | TTTCAGTGTTAAGTT[A/T]ACCTTCATTTGCACG | 8835 |
rs76427609 | snp | C/G | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93607487 | AAAGGATACACCCCA[C/G]GAAGAAGAACACAAG | 8835 |
rs76437509 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SOCS2 | GRCh38.p7 | 12:93593820 | AATCAAACCGAACCA[C/T]GCTAAAATAAAATAA | 8835 |
rs76460942 | snp | C/G | 0.067446 | 0.170804 | intron-variant | SOCS2 | GRCh38.p7 | 12:93599885 | CCCATAGAAGTGTGA[C/G]AAATAAAATTCTTCA | 8835 |
rs76566245 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | SOCS2 | GRCh38.p7 | 12:93582694 | CGGTGCAGCGGGCAC[A/T]ACCCTGAACTAGGAA | 8835 |
rs76568318 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | SOCS2 | GRCh38.p7 | 12:93596500 | GACTACCAAGAGACC[C/G]AGGCCCATGCATTTG | 8835 |
rs76627560 | snp | C/T | 0.0223435 | 0.103308 | utr-variant-3-prime, intron-variant, missense | SOCS2 | GRCh38.p7 | 12:93575523 | AGGTCCAGGCTCCAG[C/T]AGGAGAGAAAGAACT | 8835 |
rs76681885 | snp | A/C/G | 0.0252325 | 0.109451 | upstream-variant-2KB, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93569750 | TCCCAGAGCCGGCAG[A/C/G]GGGGGCACCAGGCAA | 8835 |
rs76691969 | snp | A/C | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93591277 | AACAAAAAAAAAAAA[A/C]CAAGGCTCAGCCCGA | 8835 |
rs76881897 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93608335 | TTTTCTCACTTGGCT[A/G]AAAATACAGAAGGAT | 8835 |
rs76887083 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SOCS2 | GRCh38.p7 | 12:93586890 | ACACAGTCCCTGGCC[A/G]GGCACAGTGGCTCAC | 8835 |
rs76948161 | snp | G/T | 0.5 | 0 | intron-variant, downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93581009 | TTCTCTGTTCTCTCA[G/T]TTTATTTTCCTTGTC | 8835 |
rs76961550 | snp | G/T | 0.0494327 | 0.149241 | intron-variant | SOCS2 | GRCh38.p7 | 12:93585384 | GCAAGGAGAATCAGA[G/T]GATCTCTTAGTGGTG | 8835 |
rs77101518 | snp | A/C/G | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93618032 | AGTTTCTCATGAATG[A/C/G]TTTAGCACTAACCCC | 8835 |
rs77131474 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93609573 | TATTTACTTTAATTT[A/G]TTACCTTTATTATTT | 8835 |
rs77227736 | snp | G/T | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93597345 | AATCCCTTTTTTTTT[G/T]GAGACACAGTCTTGC | 8835 |
rs77361088 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93619310 | GAAGCCAGAGAGCAA[A/G]AGAGCCTTACACAGT | 8835 |
rs77361697 | snp | C/G | 0.0663309 | 0.169604 | intron-variant | SOCS2 | GRCh38.p7 | 12:93615970 | GATAAACCAGGCTCA[C/G]AGGTGGAAAGATTTG | 8835 |
rs77472264 | snp | C/T | 0.0341408 | 0.126114 | intron-variant, downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93583922 | ATGATTTAATAGTGT[C/T]GAAAGACAAAATCAC | 8835 |
rs77641064 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93612769 | AATGAATCAATGGTG[A/G]TAGTATCATTGGTAA | 8835 |
rs77702030 | snp | C/T | 0.111576 | 0.20818 | intron-variant | SOCS2 | GRCh38.p7 | 12:93607504 | AAGAAGAACACAAGA[C/T]ACCTGCTGTAGCCCT | 8835 |
rs77724764 | snp | C/G | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93587275 | ACAATAAGATAATGG[C/G]TGCAACGGAGGTCTC | 8835 |
rs77754924 | snp | A/G | 0.136166 | 0.22258 | intron-variant | SOCS2 | GRCh38.p7 | 12:93616254 | CATTGGGGTTGCTGA[A/G]AGGATGAGATTCAAG | 8835 |
rs77762989 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SOCS2 | GRCh38.p7 | 12:93597217 | ACTGAAATCAGGATA[C/T]AGAACTATCATTACA | 8835 |
rs77771661 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SOCS2 | GRCh38.p7 | 12:93619555 | TAGGAAGCTCCTAGT[A/G]GGTGCCATGTGGGCA | 8835 |
rs77784671 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | SOCS2 | GRCh38.p7 | 12:93585670 | TTCCATTTCTCTTTC[A/G]CCTTTGTCTTCCAAA | 8835 |
rs77814697 | snp | C/T | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93601110 | TCTCTCTCTCTCTCT[C/T]TTTTTTTTTTTTAAA | 8835 |
rs77904738 | snp | C/G | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93618122 | CTCCCACTCTCTCTT[C/G]CGCCTGCTCTGGCCA | 8835 |
rs78022660 | snp | G/T | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93591823 | CGGCTGGGTGCAATG[G/T]TTTTGCCGCATATCT | 8835 |
rs78061081 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | SOCS2 | GRCh38.p7 | 12:93610103 | TGAGGATTAAGTTTT[C/T]AACATATGAACTTCA | 8835 |
rs78118487 | snp | C/G | 0.0558544 | 0.157504 | intron-variant | SOCS2 | GRCh38.p7 | 12:93609895 | AAGGTGCTGATATCT[C/G]GAGAGGGCCTTCTTG | 8835 |
rs78120333 | snp | A/G | 0.0748431 | 0.178382 | intron-variant | SOCS2 | GRCh38.p7 | 12:93601677 | GTTTTCTCAAAGAAC[A/G]AGCATTTAGATAATC | 8835 |
rs78293884 | snp | A/T | 0 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93602109 | ATTTGTTTGTTTTTT[A/T]AAATACAAGGGCTTG | 8835 |
rs78301816 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93608788 | ATGGGATGCATCCCA[C/T]TCGGTGCAACATCAG | 8835 |
rs78346014 | snp | C/T | 0.0236746 | 0.106192 | upstream-variant-2KB, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93569403 | CCCTCACCCAGAACC[C/T]GAATCTAGCCCTTCA | 8835 |
rs78364882 | snp | G/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93587276 | CAATAAGATAATGGC[G/T]GCAACGGAGGTCTCT | 8835 |
rs78374605 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93607907 | GCTTTATTACAGTTA[C/T]GGCTTCTAAAAAATT | 8835 |
rs78454769 | snp | A/G/T | 0.00318978 | 0.0398085 | intron-variant | SOCS2 | GRCh38.p7 | 12:93618124 | CCCACTCTCTCTTCC[A/G/T]CCTGCTCTGGCCATG | 8835 |
rs78470898 | snp | A/G | 0.130351 | 0.219509 | intron-variant | SOCS2 | GRCh38.p7 | 12:93624076 | AATTAAGTCATGAGA[A/G]TGAAAGCCTCATGAA | 8835 |
rs78560805 | snp | A/C | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93590235 | GCGAGACTCAGTCTC[A/C]AAAAAAAAAAAGAAT | 8835 |
rs78741312 | in-del | -/A | 0.356169 | 0.226336 | intron-variant | SOCS2 | GRCh38.p7 | 12:93584668 | AATAATGATGCTATT[-/A]TTGGGACTTTGATTT | 8835 |
rs78742602 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SOCS2 | GRCh38.p7 | 12:93582200 | CCTCAGACCTGCTGA[A/G]TGGGGAAGATCTTTT | 8835 |
rs78752261 | snp | A/T | 0.0391387 | 0.134304 | intron-variant | SOCS2 | GRCh38.p7 | 12:93618365 | ATGATAGTTTTTAAA[A/T]ATGGCTCAAATTACT | 8835 |
rs78755310 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93610334 | CTAACCTGGATGGTT[A/G]GTCACTCTGCCTGGA | 8835 |
rs78783328 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant, downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93583769 | GACTGAAAAAAGCTA[A/G]AACATTTACTAATGC | 8835 |
rs78788595 | snp | C/T | 0.0232847 | 0.105357 | intron-variant, downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93577113 | CACTGTTTTGAACAC[C/T]CTATTTCTCAGTTAC | 8835 |
rs78797763 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | SOCS2 | GRCh38.p7 | 12:93601847 | TTTTATTCCTGCTTC[C/T]TATTCCTGTCTCTAT | 8835 |
rs78802139 | snp | G/T | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93613834 | CTGTAGTCAAAATCA[G/T]AACACCACTTTGTAC | 8835 |
rs78838694 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93609925 | GCAGTATCATCCCAT[A/G]GTGGAAGGTGGAAGG | 8835 |
rs78843154 | snp | A/G | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93601328 | CACCCAAGCTGGAGT[A/G]CAGCGGTGTGGTCTC | 8835 |
rs78893675 | snp | C/T | 0.144632 | 0.226711 | intron-variant | SOCS2 | GRCh38.p7 | 12:93612881 | GGATCTATTTTACTC[C/T]TCTTCATTTCCTTCC | 8835 |
rs78938178 | snp | A/T | 0 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93587682 | CGAGACTCTGTCTAA[A/T]AAAAAAAAAAAAAAA | 8835 |
rs78939849 | snp | C/G | 0.134119 | 0.221521 | intron-variant | SOCS2 | GRCh38.p7 | 12:93622868 | GTATGTCAAGTTCAG[C/G]ATTCAGCCCTATAAA | 8835 |
rs78992544 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | SOCS2 | GRCh38.p7 | 12:93587136 | TGGCACCACTGCACT[A/C]CTGCCTGGGTGACAG | 8835 |
rs79079412 | snp | A/T | 0.093777 | 0.195178 | intron-variant | SOCS2 | GRCh38.p7 | 12:93593419 | ATACTGGAAGCAACT[A/T]GACCTTGATTTACAT | 8835 |
rs79186674 | snp | C/T | 0.0562307 | 0.157967 | downstream-variant-500B, intron-variant | SOCS2 | GRCh38.p7 | 12:93586310 | TTGTTTACTGTTTTG[C/T]TTAATTGGCTATATT | 8835 |
rs79219079 | snp | G/T | 0.193653 | 0.243567 | intron-variant | SOCS2 | GRCh38.p7 | 12:93624098 | CCTCATGAATGGGAT[G/T]AGCCGCCTTGTAAAA | 8835 |
rs79281869 | in-del | -/AC | 0.170408 | 0.236992 | intron-variant | SOCS2 | GRCh38.p7 | 12:93621330 | TTGGGAAGGGAAATT[-/AC]ACAGACTGTCTATCA | 8835 |
rs79359277 | snp | A/C | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93604207 | CAAACAAAACAAAAC[A/C]AAAAAAACAAGAAAA | 8835 |
rs79471987 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | SOCS2 | GRCh38.p7 | 12:93622489 | GATGCCTCCAAAGGC[C/T]CACACATGTCACATG | 8835 |
rs79519700 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SOCS2 | GRCh38.p7 | 12:93582812 | TCAGGATTTTTGGTC[C/T]CTTCCAAGGAGGTCC | 8835 |
rs79583873 | snp | C/T | 0.0926964 | 0.194308 | intron-variant | SOCS2 | GRCh38.p7 | 12:93608135 | ACTCCTCAAACTCCA[C/T]GTGCCAACATGCCTG | 8835 |
rs79698855 | snp | A/C | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93590234 | AGCGAGACTCAGTCT[A/C]AAAAAAAAAAAAGAA | 8835 |
rs79699574 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | SOCS2 | GRCh38.p7 | 12:93593251 | ATCTAGATCCTGCCT[C/T]CAGTGGGATAGCTGA | 8835 |
rs79727543 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SOCS2 | GRCh38.p7 | 12:93592840 | TTCACAGCTATGGGA[C/T]AGGCACATGGCTCTA | 8835 |
rs79790991 | snp | C/G | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93624737 | AGGCATCAGAAATTG[C/G]TGGAACCCATTAAGT | 8835 |
rs79824962 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | SOCS2 | GRCh38.p7 | 12:93579258 | CTATCATAAAGTTGC[A/C]CTCTTGACTTATCTA | 8835 |
rs79861289 | snp | A/T | 0.0618563 | 0.164627 | intron-variant | SOCS2 | GRCh38.p7 | 12:93605047 | CCCACTCCCCACTCC[A/T]GCCCCAGTAGTCTTG | 8835 |
rs79922270 | snp | A/T | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93588614 | ATTCTGGAGACAGTG[A/T]ATTTTTTTTTTTTTT | 8835 |
rs79923997 | snp | A/C | 0.0372196 | 0.131242 | intron-variant | SOCS2 | GRCh38.p7 | 12:93606448 | TTTGTGGAACTGCTG[A/C]GGTGTGGCTTTATTT | 8835 |
rs79951907 | snp | C/T | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93611844 | TTGGTAAGACTTCCT[C/T]TGATATTCAGTTTAT | 8835 |
rs80140774 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | SOCS2 | GRCh38.p7 | 12:93602466 | TGTGTATGTATAAAG[C/T]CATGTGACCTGTACA | 8835 |
rs80221304 | snp | A/G | 0.106987 | 0.205054 | intron-variant | SOCS2 | GRCh38.p7 | 12:93624201 | AGGTGCCATCTTGAA[A/G]GCAAAGACTAGGCCC | 8835 |
rs80230203 | snp | C/T | 0.125874 | 0.217008 | intron-variant | SOCS2 | GRCh38.p7 | 12:93619739 | TTTTCCCTTGCATTA[C/T]ACTAAACATATATTG | 8835 |
rs80253030 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | SOCS2 | GRCh38.p7 | 12:93599161 | TCCAGTTTGCTGTTG[C/T]GCTGTTTGTCTTTTT | 8835 |
rs80270853 | snp | A/C | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93610201 | AACAGTCGTTCTCAG[A/C]CTTTAGCACACATAA | 8835 |
rs80288416 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | SOCS2 | GRCh38.p7 | 12:93620946 | TTCATCTATCCATTC[A/G]TCCAGCCATATCCAT | 8835 |
rs80304443 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93609889 | AATGTCAAGGTGCTG[A/G]TATCTGGAGAGGGCC | 8835 |
rs80307508 | snp | C/T | 0.345037 | 0.231231 | intron-variant | SOCS2 | GRCh38.p7 | 12:93624329 | TGTAATCCCAGCACT[C/T]TGGGAGGCCAAGGCG | 8835 |
rs80336003 | snp | G/T | 0 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93584779 | CCCTTCTTTTTTTTT[G/T]GAGACGGAGTTTCGC | 8835 |
rs80339196 | snp | A/T | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93601122 | TCTTTTTTTTTTTTT[A/T]AAATATACCTTCTGT | 8835 |
rs111403434 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SOCS2 | GRCh38.p7 | 12:93610603 | GAAAGTGATTGAGTC[A/G]TGGGCACTCCAGTTC | 8835 |
rs111413769 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SOCS2 | GRCh38.p7 | 12:93617495 | CTAAGTATATTATGT[C/T]TGAATAAAAACACCA | 8835 |
rs111429552 | in-del | -/T | 0.0554779 | 0.157039 | intron-variant | SOCS2 | GRCh38.p7 | 12:93611233 | ACTGTCAAAAAATGA[-/T]TTTTTTTTTCTTTTT | 8835 |
rs111510458 | snp | A/C | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93608376 | ATGTATATAGGAGGG[A/C]ACATTTTTCTTTTGC | 8835 |
rs111535168 | snp | C/T | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93588868 | CTCAGGTGATCCACC[C/T]GCCTCGGCCTCCCAA | 8835 |
rs111651314 | snp | C/T | 0.348134 | 0.229934 | intron-variant | SOCS2 | GRCh38.p7 | 12:93624515 | AGGCGGAGGTTGTAG[C/T]GAGCCGAGATTGCAC | 8835 |
rs111704122 | snp | C/T | 0.0228947 | 0.104514 | utr-variant-3-prime, intron-variant, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93585903 | GTATTTGCATATAAC[C/T]GGCATACACCCTCAC | 8835 |
rs111821921 | in-del | -/T | 0 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93604964 | CTGTGCCGGCCTGGA[-/T]TTTTTTTTTTTTTTA | 8835 |
rs111894516 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SOCS2 | GRCh38.p7 | 12:93601448 | GCCGGCTTTTCAGTA[A/G]AGACTGGGTTTCATC | 8835 |
rs111896883 | snp | A/G | 0 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93587022 | AAATTACAAAAATTC[A/G]CCAGGTGTGATGGCG | 8835 |
rs112044920 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | SOCS2 | GRCh38.p7 | 12:93609317 | GAATTGCTTGAACCC[A/G]GGAGACAGAGGTTGG | 8835 |
rs112321815 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | SOCS2 | GRCh38.p7 | 12:93601600 | AGGCGAGAGCCACAG[C/T]GCCTGGCCAAAGTCT | 8835 |
rs112387889 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | SOCS2 | GRCh38.p7 | 12:93602780 | CTGCCTCAGAGCCCT[C/G]CATTCTGTAATCCAC | 8835 |
rs112534840 | snp | C/T | 0.125874 | 0.217008 | intron-variant | SOCS2 | GRCh38.p7 | 12:93614635 | TTTCTTTCTTTCTTT[C/T]GATGGAGTCTGGCTC | 8835 |
rs112568023 | snp | A/C/G | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93614627 | TTTCTTTCTTTCTTT[A/C/G]TTTCTTTTGATGGAG | 8835 |
rs112591498 | snp | A/C | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93571209 | CGCAGCTCGGGCGCC[A/C]GCGGCAGGTACCGGT | 8835 |
rs112649565 | in-del | -/T/TT | 0.0879971 | 0.190408 | intron-variant | SOCS2 | GRCh38.p7 | 12:93601108 | ATCTCTCTCTCTCTC[-/T/TT]TTTTTTTTTTTTTTA | 8835 |
rs112802913 | snp | A/T | 0.0547245 | 0.156101 | intron-variant | SOCS2 | GRCh38.p7 | 12:93600175 | TAAAGGTATAGATTT[A/T]AAAAAAATTATTTTT | 8835 |
rs112898345 | snp | A/G | 0.0452528 | 0.143452 | intron-variant, downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93580806 | GTGGCCATCAATTCT[A/G]TATTTGGTCAGAAAG | 8835 |
rs112966105 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SOCS2 | GRCh38.p7 | 12:93616009 | CTCATGATTAATTCA[C/T]GGCTAAGGAAGATAT | 8835 |
rs113066114 | snp | C/T | 0.100588 | 0.200439 | intron-variant | SOCS2 | GRCh38.p7 | 12:93602284 | TATTTTTAGTAGAGA[C/T]GAGGTCTCACTATGT | 8835 |
rs113146609 | snp | A/G | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93587457 | GAGGCAGAGGTGGGC[A/G]GATCACGAGGTCAGG | 8835 |
rs113219963 | snp | G/T | 0 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93591234 | GGTTAGAAAGGGAGG[G/T]GTTTTTTAAAAAAAA | 8835 |
rs113237581 | snp | A/G | 0.0748431 | 0.178382 | intron-variant | SOCS2 | GRCh38.p7 | 12:93601593 | GGATTACAGGCGAGA[A/G]CCACAGCGCCTGGCC | 8835 |
rs113288423 | snp | C/G | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93574556 | TTTATTAAATTCCTA[C/G]TGAAAGTATTTGTGG | 8835 |
rs113302281 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | SOCS2 | GRCh38.p7 | 12:93605246 | ATCGCTCTCTTAAAC[A/G]AGCAAGTTGCCGAGT | 8835 |
rs113434526 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | SOCS2 | GRCh38.p7 | 12:93619388 | GGCACAGGGCAGGAT[C/G]GGAGCAAACAGAGCC | 8835 |
rs113449431 | snp | G/T | 0 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93581145 | TCAATTACTAAAAAC[G/T]GAGAGATTTTGTGAG | 8835 |
rs113505520 | snp | C/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93614498 | CCTTCCTTCCTTCCT[C/T]CCTTCCTTCCTTCCT | 8835 |
rs113621885 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93569823 | GCCCAACTTCCCATA[C/G]CCGCGGCCTCAACTA | 8835 |
rs113822324 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SOCS2 | GRCh38.p7 | 12:93597248 | AAGATCTCCTTTGTG[C/T]TACCCATTTATAGTG | 8835 |
rs113944276 | snp | G/T | 0.5 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93595909 | TAATTTGTTTTTAAT[G/T]TTTTTTTATGTGATT | 8835 |
rs114119017 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93607149 | ATCCTTTAATAAAAT[A/G]TGTGTTCTTTTTCTA | 8835 |
rs114158193 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant, downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93583697 | CCATGGGTTTTATTA[C/T]GTCCAAGGCGTGACA | 8835 |
rs114165667 | snp | A/G | 0.029116 | 0.117091 | downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93626577 | TTCCAAATAGCACCA[A/G]AACTTTTCATCCACC | 8835 |
rs114170397 | snp | C/T | 0.0228947 | 0.104514 | downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93626262 | ATAAATGCAATAGAA[C/T]GCTACCTTTGCTGAA | 8835 |
rs114177746 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SOCS2 | GRCh38.p7 | 12:93597656 | TTTTTGTATTATGAA[A/G]TAGCTCATCAGAAAA | 8835 |
rs114182068 | snp | A/G | 0.0123036 | 0.0774623 | utr-variant-3-prime, intron-variant | SOCS2 | GRCh38.p7 | 12:93576233 | TGAGTTCTAGAGAAC[A/G]TACACTTTCATGGTA | 8835 |
rs114192246 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | SOCS2 | GRCh38.p7 | 12:93596517 | GGCCCATGCATTTGA[A/T]CTCTTGAATGTTCAA | 8835 |
rs114349841 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | SOCS2 | GRCh38.p7 | 12:93610139 | TACGTTCAAACTATA[A/G]CACCCACCATATTAT | 8835 |
rs114433657 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | SOCS2 | GRCh38.p7 | 12:93620906 | GTATATGCAGATAGA[C/T]GGATACCTTTGGGAA | 8835 |
rs114448484 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | SOCS2 | GRCh38.p7 | 12:93618870 | AGGGTACCAGCAAGG[C/T]GTCTCACTATGTTGC | 8835 |
rs114572225 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93593387 | AAGAAAAGCAAACAA[A/G]TAGGGCTCAGCCTGA | 8835 |
rs114659994 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SOCS2 | GRCh38.p7 | 12:93616680 | GCTGCATTTCAATGG[A/G]CGGGGGTATGTGTGC | 8835 |
rs114716595 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | SOCS2 | GRCh38.p7 | 12:93606058 | GTCAAGGATCCAAGC[A/T]CCTCCTATCTTGTTG | 8835 |
rs114719581 | snp | A/G | 0.030278 | 0.119257 | intron-variant | SOCS2 | GRCh38.p7 | 12:93600825 | ATGAGGTCTTGATCT[A/G]TCACCCGGGCTGGAG | 8835 |
rs115170630 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | SOCS2 | GRCh38.p7 | 12:93617954 | CCACCCAAATCTCAC[A/G]TCAAATTATAATCCC | 8835 |
rs115185597 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SOCS2 | GRCh38.p7 | 12:93607081 | TGATTCAGATTATAC[C/T]TGGCTTCTGGTTAGG | 8835 |
rs115291104 | snp | C/T | 0.030278 | 0.119257 | intron-variant | SOCS2 | GRCh38.p7 | 12:93623200 | GTGAGGGAGTTCTCA[C/T]GAGATCTGATGGTTT | 8835 |
rs115386357 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93608202 | GACAGGGTCTTGTTA[C/T]ATTGGCCAGGCTGGT | 8835 |
rs115400781 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SOCS2 | GRCh38.p7 | 12:93605298 | ACGTATATAAGATAA[A/G]AAATTACCCCAAAGT | 8835 |
rs115459957 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SOCS2 | GRCh38.p7 | 12:93598233 | GATGCCTTAACGTAA[A/G]GATGAGTTTGGTTTG | 8835 |
rs115573923 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SOCS2 | GRCh38.p7 | 12:93611001 | CTCAATTTTTAGAAC[C/T]CCACAGGGTTCCTTA | 8835 |
rs115583840 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | SOCS2 | GRCh38.p7 | 12:93581785 | GTTCTTTCATTGAGG[C/G]AGCTCTTACAGACCA | 8835 |
rs115608251 | snp | A/G | 0.0232847 | 0.105357 | utr-variant-3-prime, intron-variant | SOCS2 | GRCh38.p7 | 12:93576408 | ATTGTCAAGTGGCCG[A/G]GTCTTTTATAATTTG | 8835 |
rs115615036 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | SOCS2 | GRCh38.p7 | 12:93604930 | CCCCCGCAAAGTGCT[A/G]GGATTACAGGTGTCA | 8835 |
rs115937694 | snp | A/G | 0.0633504 | 0.166319 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93572095 | GCCGCGGCACCCCCA[A/G]CCCCGCCAGAGCGGG | 8835 |
rs116039697 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SOCS2 | GRCh38.p7 | 12:93616477 | TGTTTATTTCTTGCT[C/T]AGTCAAGTTTCTGTC | 8835 |
rs116070095 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93581079 | AAAAAAATATCAAGA[A/G]AGAAAAGTAAGGGAG | 8835 |
rs116170279 | snp | C/T | 0.0333695 | 0.124785 | upstream-variant-2KB, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93570358 | AAGGACGGCCGGCGC[C/T]GCTTAAGGAGGCGCT | 8835 |
rs116188098 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | SOCS2 | GRCh38.p7 | 12:93600304 | TTTCCATAAGCATGG[G/T]TCTGTTTATGAGCTC | 8835 |
rs116195505 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SOCS2 | GRCh38.p7 | 12:93623178 | CTCCCAGGCTGGTCT[C/T]GTGATAGTGAGGGAG | 8835 |
rs116289397 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | SOCS2 | GRCh38.p7 | 12:93598106 | TATAGGATATCAGAC[C/T]GGCAGGGAAAGTGGG | 8835 |
rs116355041 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | SOCS2 | GRCh38.p7 | 12:93606429 | TAGGTCACACAGTTA[A/G]TACTTTGTGGAACTG | 8835 |
rs116410387 | snp | A/C | 0.0539704 | 0.155153 | downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93626348 | CCTCCCTCTACCCCC[A/C]CTGCAACCTCCCAAC | 8835 |
rs116411140 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SOCS2 | GRCh38.p7 | 12:93605220 | AAGGATAGTTGTTGC[A/G]GCTTGTCTTTATCGC | 8835 |
rs116431571 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93583235 | TGGAAGGCTGTCTTC[A/G]CTCTGCTTCCCAGCT | 8835 |
rs116514367 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | SOCS2 | GRCh38.p7 | 12:93593636 | TTATAGCCAACTTTT[G/T]GGGAATTACAGGACT | 8835 |
rs116655549 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | SOCS2 | GRCh38.p7 | 12:93617119 | GATATGCTAAGCAGA[C/T]TGTCTTATGCTTTGG | 8835 |
rs116657400 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | SOCS2 | GRCh38.p7 | 12:93576124 | AGATACAGGGGGATA[C/T]CTGCCTGTTTTTCAA | 8835 |
rs116724407 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SOCS2 | GRCh38.p7 | 12:93623525 | GCTGGTGTGCTGCAC[C/T]GGGAAGTTCTTTATA | 8835 |
rs116742817 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | SOCS2 | GRCh38.p7 | 12:93618776 | ATCCAAAGCTATTAT[A/G]TTAATATGGTTGTTT | 8835 |
rs116752290 | snp | A/T | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93608295 | CATGAACCACCATAC[A/T]TGGCAATGTTAAGCT | 8835 |
rs116829380 | snp | A/G/T | 0.0244538 | 0.107838 | intron-variant | SOCS2 | GRCh38.p7 | 12:93588646 | TTGAGCCAGAGTCTC[A/G/T]CTCTGTTGCCCAGAG | 8835 |
rs116897931 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SOCS2 | GRCh38.p7 | 12:93591520 | GGAGTTCCTGCAGGG[A/G]CTGGCTCTAGCGTCT | 8835 |
rs116944126 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93597961 | AAGTCAACAAATATA[C/T]ATTGAGTGCCTACTG | 8835 |
rs117099118 | snp | C/T | 0.0146672 | 0.084371 | downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93626334 | CCTTATCTTGCTGGC[C/T]TCCCTCTACCCCCAC | 8835 |
rs117173193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93621877 | TTCTGAGACTTAAAT[C/T]AGTTAACATATGAAC | 8835 |
rs117288619 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SOCS2 | GRCh38.p7 | 12:93622901 | TATGGAAGGTTTGAG[C/T]CATGACTAGTTTAGG | 8835 |
rs117405874 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93579157 | CGACTGCCCGCCCTC[C/G]CATCCTTACCAGCAG | 8835 |
rs117428887 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | SOCS2 | GRCh38.p7 | 12:93601713 | AAGTCTCTCTTCCAA[A/T]CTCTGTGATATATGA | 8835 |
rs117486083 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | SOCS2 | GRCh38.p7 | 12:93593696 | TGCTTATCTGGAAAA[C/T]AACCCTAGTAAGACC | 8835 |
rs117703732 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SOCS2 | GRCh38.p7 | 12:93621140 | TCCTAGTCAAGACTA[C/T]ATAGATTCCATGTAT | 8835 |
rs117728358 | snp | C/G/T | 0.0229589 | 0.105107 | intron-variant | SOCS2 | GRCh38.p7 | 12:93599520 | GTAAACAATCCTTCG[C/G/T]TGGATTTTAAGCATT | 8835 |
rs117743355 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SOCS2 | GRCh38.p7 | 12:93593172 | GATTTCCTACAACTG[A/G]AAGGTGGTTCTGGAG | 8835 |
rs117805055 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SOCS2 | GRCh38.p7 | 12:93588983 | GGGGTACGCATAGAC[A/C]CCATTTCCTCCAGCA | 8835 |
rs117846542 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93585376 | GCTGATGGGCAAGGA[C/G]AATCAGAGGATCTCT | 8835 |
rs117914504 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant, downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93577241 | GACAGCACAAACATC[A/T]CTGGAGTGTGCCATG | 8835 |
rs117934565 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SOCS2 | GRCh38.p7 | 12:93604276 | ATGTGAAAAGCAGAC[A/G]ACATTCTTACATGAA | 8835 |
rs118030876 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SOCS2 | GRCh38.p7 | 12:93591425 | AGCGTGTGTGCGTTC[A/G]TGTGTGGCTGTCTGT | 8835 |
rs137904057 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93573869 | TTGTGGGGGTGGGGG[C/G]AGCACAAATGTTCAG | 8835 |
rs137938143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93608678 | TTAGCAATTTTTGGT[A/G]TTATTTCTGACAATG | 8835 |
rs138001966 | in-del | -/GG | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93578713 | ACACACACACACACA[-/GG]CACACAACCCAGCCA | 8835 |
rs138058831 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SOCS2 | GRCh38.p7 | 12:93601419 | AGCTGGGATTACAGG[C/T]GCCCACCACCATGGC | 8835 |
rs138229144 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SOCS2 | GRCh38.p7 | 12:93596401 | AATACCTGATTTAAT[A/G]TTTAATATTTGGGAT | 8835 |
rs138306287 | snp | C/G | 0.00194363 | 0.0311133 | utr-variant-3-prime, intron-variant, missense | SOCS2 | GRCh38.p7 | 12:93575519 | TCAAAGGTCCAGGCT[C/G]CAGTAGGAGAGAAAG | 8835 |
rs138341479 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SOCS2 | GRCh38.p7 | 12:93624390 | ATCCTGACCAACATG[A/G]TGAAACCTTGTCTCT | 8835 |
rs138438342 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93612050 | CTTTTCCATGTAGCT[C/T]CAGGGAATGTTGTTC | 8835 |
rs138510220 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | SOCS2 | GRCh38.p7 | 12:93579490 | TTTTAAGTATGGCAG[C/G]CTCCTTTTTCAGTGT | 8835 |
rs138517254 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SOCS2 | GRCh38.p7 | 12:93623768 | CAGGAGTGCAATCGC[A/G]ATCTCAGCTCACTGC | 8835 |
rs138597707 | in-del | -/AGTA | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93607948 | TTATGGAAGAAAATT[-/AGTA]AGTCTGTCAACTAAA | 8835 |
rs138598392 | in-del | -/CCAA | 0.0256215 | 0.110247 | intron-variant | SOCS2 | GRCh38.p7 | 12:93621120 | GTCCTCGTGACTGTT[-/CCAA]CTCCTAGTCAAGACT | 8835 |
rs138606476 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | SOCS2 | GRCh38.p7 | 12:93609119 | TAAATAGGCCAGGTA[C/T]GGTGGCTCATGCCTG | 8835 |
rs138839504 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SOCS2 | GRCh38.p7 | 12:93595537 | GGAATGCTTTTCTTC[A/G]GCCAACTGAAAGTAG | 8835 |
rs138840210 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93589071 | GCTATCATTATTTAC[C/T]GTACAGCATGGTTTA | 8835 |
rs138877924 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SOCS2 | GRCh38.p7 | 12:93608224 | CAGGCTGGTCTCGAA[C/T]TCCTGTCCTCAAGTG | 8835 |
rs138915477 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93569206 | AGGAATAAATACCTT[C/T]TTATTTAAGCTAAAG | 8835 |
rs138921590 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SOCS2 | GRCh38.p7 | 12:93614984 | GGTCATTGAGCAGCC[A/G]GCAAAGGATCCTAGG | 8835 |
rs138945432 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SOCS2 | GRCh38.p7 | 12:93602034 | CATTCTAGACATATT[A/G]CAGATTGCAAGATGG | 8835 |
rs139130191 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93613921 | TTTAAAGCTGGTACC[C/G]TCCCAAAAAAGAATA | 8835 |
rs139284830 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant, utr-variant-3-prime | SOCS2 | GRCh38.p7 | 12:93580367 | TGGCTCATGCCTGCA[A/G]TCCCAGCACTTTGGG | 8835 |
rs139300069 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SOCS2 | GRCh38.p7 | 12:93582709 | AACCCTGAACTAGGA[A/G]TTGGAAAACTTGGGG | 8835 |
rs139332088 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93580682 | TTATTTCTACCCAGA[A/G]AAAGTTGTTTGACTT | 8835 |
rs139367170 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | SOCS2 | GRCh38.p7 | 12:93579873 | AATAGGACTTACTTC[A/C/G]ATAAACATGCATTTG | 8835 |
rs139375613 | snp | A/G | 3.40246e-05 | 0.00412446 | missense, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93575108 | ATTAACAAATGTACC[A/G]GTGCCATCTGGGGAC | 8835 |
rs139400296 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SOCS2 | GRCh38.p7 | 12:93577905 | TCCTCACCAAAGCCT[A/G]GAAGAATATCCAGTG | 8835 |
rs139414556 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SOCS2 | GRCh38.p7 | 12:93620720 | TGCCTGGCCTGGAGC[A/G]ACATTTATTCCTATG | 8835 |
rs139504140 | in-del | -/A | | | utr-variant-3-prime, intron-variant | SOCS2 | GRCh38.p7 | 12:93575196 | TGTTTCTCTTTTTTT[-/A]AACATGTCTCACATA | 8835 |
rs139620473 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SOCS2 | GRCh38.p7 | 12:93616821 | ATGAATAAGAATTGG[C/T]GGGCAGGAGATGGGG | 8835 |
rs139710881 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | SOCS2 | GRCh38.p7 | 12:93609903 | GATATCTGGAGAGGG[C/G]CTTCTTGCAGTATCA | 8835 |
rs139753378 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SOCS2 | GRCh38.p7 | 12:93609409 | AAAATAAATAAGTAA[A/G]TAAATAAATAAAGAC | 8835 |
rs139760629 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SOCS2 | GRCh38.p7 | 12:93605514 | AATAGTTGTTGATCC[C/T]TGGAGATTTTCAGTG | 8835 |
rs139766957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93619389 | GCACAGGGCAGGATC[A/G]GAGCAAACAGAGCCT | 8835 |
rs139899210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93615667 | GTGGCACCATGTCAT[C/T]TCACTACAACCTCCA | 8835 |
rs139940011 | in-del | -/CTT | 0.0130921 | 0.0798413 | intron-variant, cds-indel | SOCS2 | GRCh38.p7 | 12:93579945 | GACCCACATCCTTAA[-/CTT]ATAGGCATTCTGACT | 8835 |
rs139955332 | in-del | -/ATTTTTTTTTTTTTTATTTTTTTTC | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93581413 | ACAATTCAAGGAATG[-/ATTTTTTTTTTTTTTATTTTTTTTC]ATTTTTTTTTTTTTT | 8835 |
rs139967048 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SOCS2 | GRCh38.p7 | 12:93613065 | CCAATTCAGGAACTC[C/T]GGCACTTCTTTCTAT | 8835 |
rs139981789 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SOCS2 | GRCh38.p7 | 12:93581440 | TTTTAATGTGTGTCA[A/C]TCTTATATTGGGTTA | 8835 |
rs140084496 | snp | C/G/T | 6.60452e-05 | 0.0057462 | missense, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93575006 | CGGACAGGTCCAGAA[C/G/T]CCCCCCGGAACGGCA | 8835 |
rs140149365 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SOCS2 | GRCh38.p7 | 12:93603384 | CAAAAAGGTTAGGCC[C/T]TCTGCCTCAAGTCAC | 8835 |
rs140181201 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93598140 | GTGAGGGGATTGGCA[A/G]GGCACCGAGGAAACA | 8835 |
rs140195205 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SOCS2 | GRCh38.p7 | 12:93582180 | GTTAATAGACTGGAA[A/G]GAGTCCTCAGACCTG | 8835 |
rs140216374 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93568063 | CAAGGTGCTGAACTA[C/G]AGCTGTGAACAATGC | 8835 |
rs140391646 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93591658 | GAGCTGTGGCGTGGC[A/G]GCTCCTCCCAGACGC | 8835 |
rs140477212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93598952 | CCAATTATTGTCCCT[A/G]GTGCCTAGCTGTTTA | 8835 |
rs140583971 | in-del | -/CATATA | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93608571 | TGATATTACATAGTT[-/CATATA]CATATACTTCATATA | 8835 |
rs140678130 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93611324 | CTCACTGCAACCTCC[A/G]CCTCCTTGGTTCAAG | 8835 |
rs140743528 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SOCS2 | GRCh38.p7 | 12:93575915 | GCTATACAGGTGCAA[C/T]TCAATCCCCGTTAAT | 8835 |
rs140774313 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SOCS2 | GRCh38.p7 | 12:93622383 | CACAAAAGTGTTGTC[A/G]GAGACTCTTGCTCCT | 8835 |
rs140833686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93578422 | TGTGAGTTTAGGCAC[A/G]GGGTAGGTGGGGTTT | 8835 |
rs140848685 | snp | A/C | 0.000121175 | 0.00778287 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93572824 | GATTCGCACTGACTT[A/C]AAGGAAGGACGCGAA | 8835 |
rs140970388 | in-del | -/GTGA | 0.0197687 | 0.0974348 | intron-variant | SOCS2 | GRCh38.p7 | 12:93606184 | CCAGAATTTAATCAT[-/GTGA]GTGCATCTGGCTGCA | 8835 |
rs140995506 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SOCS2 | GRCh38.p7 | 12:93600705 | TAAATCTGTTTATAA[A/G]TTACGTAAAGTTTTT | 8835 |
rs141098044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93594485 | AGTCCATTAAGACTT[C/T]AGAAGATATTCTTTC | 8835 |
rs141386059 | in-del | -/A | 0.125874 | 0.217008 | intron-variant | SOCS2 | GRCh38.p7 | 12:93620155 | CTTTTTTTGTTTAAG[-/A]AAAAAAAATCACTTA | 8835 |
rs141399995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SOCS2 | GRCh38.p7 | 12:93579874 | ATAGGACTTACTTCA[A/G]TAAACATGCATTTGT | 8835 |
rs141445763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93608554 | ATCTGTAAAACTGAG[A/G]ATGATATTACATAGT | 8835 |
rs141460928 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SOCS2 | GRCh38.p7 | 12:93624103 | TGAATGGGATTAGCC[A/G]CCTTGTAAAAGGTCT | 8835 |
rs141501762 | snp | A/G | 0.000148604 | 0.00861859 | missense, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93575013 | GTCCAGAAGCCCCCC[A/G]GAACGGCACTGTTCA | 8835 |
rs141552388 | in-del | -/G | 0.0704125 | 0.17392 | intron-variant | SOCS2 | GRCh38.p7 | 12:93589843 | TTATTAGAACTTTGT[-/G]GCAAAACTTTTTCTC | 8835 |
rs141581637 | in-del | -/A | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93604206 | CAAACAAAACAAAAC[-/A]AAAAAAAACAAGAAA | 8835 |
rs141648122 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93610215 | GACTTTAGCACACAT[A/T]AGAATCATGTGGAGC | 8835 |
rs141683231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93611897 | CACAAAGGAGGCCTC[C/T]GTTGGTTTGCTTCTC | 8835 |
rs141693516 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | SOCS2 | GRCh38.p7 | 12:93624448 | GTGGTGGCAGGCACC[G/T]GTAGTCCCAGCTACT | 8835 |
rs141702204 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SOCS2 | GRCh38.p7 | 12:93602891 | CCAGGTTGTCATCTG[A/G]GTCCTTTCCATCTTT | 8835 |
rs141724365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93623213 | CACGAGATCTGATGG[C/T]TTAAGTGCCAAGAAG | 8835 |
rs141931173 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | SOCS2 | GRCh38.p7 | 12:93614705 | ACTGCTACCTCTGCC[C/T]CCTGGGTTCAAGCGA | 8835 |
rs142068421 | snp | A/G | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93625166 | GGTCATCTCCTGGGG[A/G]AGCCAAATAGTTTTA | 8835 |
rs142095690 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | SOCS2 | GRCh38.p7 | 12:93609168 | AGGCCGAGGCAGGCA[A/G]ATCACCTGAGTTCAG | 8835 |
rs142112015 | snp | A/C/G/T | 0.000198483 | 0.0099604 | missense, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93575055 | CCAAACCGCTCTACA[A/C/G/T]GTCAGCACCATCTCT | 8835 |
rs142133132 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93607965 | GTCTGTCAACTAAAT[A/T]TTGTTTTTAGTAGTT | 8835 |
rs142141849 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SOCS2 | GRCh38.p7 | 12:93577554 | CGGGAGAGGAATTGG[A/G]AAGAGCAAATTGCTG | 8835 |
rs142198425 | in-del | -/TT | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93601121 | TCTTTTTTTTTTTTT[-/TT]TAAATATACCTTCTG | 8835 |
rs142248036 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93612823 | CTCCTTTCTTTAAAG[G/T]CAATGTAACCCCTAC | 8835 |
rs142465376 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93568753 | ATGCAGCCATCAGGG[C/T]TGGAGCATTCTAGGA | 8835 |
rs142475701 | in-del | -/C | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93599779 | GCTCTCTTGCACATG[-/C]ATGCTGTCTTGCTCT | 8835 |
rs142502822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93582573 | TGCCCTGGAGTATGC[A/G]GCTTTGAGTCACACA | 8835 |
rs142519563 | snp | G/T | 0.02016 | 0.0983543 | utr-variant-3-prime, intron-variant, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93586277 | AAGATAAATAAATTA[G/T]GTTCACATTCACTCC | 8835 |
rs142528314 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SOCS2 | GRCh38.p7 | 12:93585054 | AGGTGTGAGCCATCA[C/T]GCCTGGCCATTCCTC | 8835 |
rs142595927 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SOCS2 | GRCh38.p7 | 12:93616061 | GGCCCTGTGGGGAAT[C/G]AGCCCTTCCCACTCT | 8835 |
rs142616345 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93626085 | GACGGTTCTGCCAAA[C/G]GTTTGGTTCTTTCCA | 8835 |
rs142654914 | in-del | -/T | 0.144632 | 0.226711 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93572213 | GGGGCCCCGCAGCGC[-/T]TTAGGGCGGAGAACC | 8835 |
rs142681328 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | SOCS2 | GRCh38.p7 | 12:93602164 | GTGGCGCGATCACAG[C/T]TGCCTGAAGCCTCCA | 8835 |
rs142742956 | snp | A/C/T | 0.00239401 | 0.0345304 | intron-variant | SOCS2 | GRCh38.p7 | 12:93596809 | CTCTAGACTGGGAGA[A/C/T]GGAGCAAGACCCTGT | 8835 |
rs142764815 | snp | C/T | 0.000181239 | 0.00951769 | synonymous-codon, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93574898 | GACGGAAAATTCAGA[C/T]TGGACTCTATCATAT | 8835 |
rs142909715 | in-del | -/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93589360 | GGGAATTTTTTTTTT[-/T]AAATTCCCATGGGTT | 8835 |
rs142930099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93593235 | GCTGACCCGACTCTA[C/T]ATCTAGATCCTGCCT | 8835 |
rs143000020 | snp | C/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93609466 | TATTTTATTAATTTA[C/T]TAATTTTTATTACCT | 8835 |
rs143093209 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SOCS2 | GRCh38.p7 | 12:93574007 | TTGGGTTTGGATTAG[A/G]GCAAAGTTCAAAAGA | 8835 |
rs143236537 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SOCS2 | GRCh38.p7 | 12:93623790 | GCTCACTGCAACCTC[C/T]GCCTCCCGAGCTCAA | 8835 |
rs143304098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93606683 | TTTGGGACAGGGTCT[C/T]GCTCTGTCACCCAGG | 8835 |
rs143393268 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SOCS2 | GRCh38.p7 | 12:93619801 | TGCATCCCTCCCATT[C/T]CTGCCTGGAATGCTC | 8835 |
rs143421721 | in-del | -/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93611242 | AAAATGATTTTTTTT[-/T]CTTTTTGAGACAGGA | 8835 |
rs143514327 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SOCS2 | GRCh38.p7 | 12:93616955 | TTTTATTGTTAACCT[C/T]TCATGACTCACCTAA | 8835 |
rs143551202 | snp | A/G | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93590822 | AAAAAAAAAAAAAAA[A/G]GTTAGCTTCCCAGTG | 8835 |
rs143553352 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93596507 | AAGAGACCCAGGCCC[A/G]TGCATTTGATCTCTT | 8835 |
rs143622626 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | SOCS2 | GRCh38.p7 | 12:93611237 | GTCAAAAAATGATTT[G/T]TTTTTCTTTTTGAGA | 8835 |
rs143709484 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SOCS2 | GRCh38.p7 | 12:93601850 | TATTCCTGCTTCCTA[C/T]TCCTGTCTCTATTGA | 8835 |
rs143773074 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93596680 | TAAAAATACAAAAAT[G/T]AGCTGGGCGTGTTGG | 8835 |
rs143789914 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93619000 | ATTCTTAAAGGAGTT[A/C/T]AACTGAAGGGAATTT | 8835 |
rs143816787 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | SOCS2 | GRCh38.p7 | 12:93604032 | TACACAGAACACCCA[C/T]ATGGAGGCAACATGC | 8835 |
rs143852237 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SOCS2 | GRCh38.p7 | 12:93615843 | TCAAGTGATCCTCCC[A/G]CCTCGGCCTCCCAAA | 8835 |
rs143932508 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SOCS2 | GRCh38.p7 | 12:93598179 | ACGATACTGTGTTTT[C/T]GATCAAAACCTGATT | 8835 |
rs143961727 | snp | C/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93621249 | AAAATACCAAACTGT[C/T]TTTCTTTAGCATCAG | 8835 |
rs144017702 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93619602 | TTGTTTAATCCACAC[A/C]GGAATCCTATGAGAT | 8835 |
rs144048599 | in-del | -/G | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93578445 | GGGGTTTGAGTGGCT[-/G]GTGGTTATGTCTAAC | 8835 |
rs144073968 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, utr-variant-3-prime | SOCS2 | GRCh38.p7 | 12:93579527 | AACCTTCATTTGCAC[A/G]GAATAAAAATGCCCT | 8835 |
rs144140054 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SOCS2 | GRCh38.p7 | 12:93581237 | CAGAAATAGGCAGAT[A/G]CTATAAATTAAGACT | 8835 |
rs144141601 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | SOCS2 | GRCh38.p7 | 12:93575665 | ATGTACCTAGGAGTT[G/T]TGTTAAACAGATGAT | 8835 |
rs144172793 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93624664 | TACTCATCACCCAAG[G/T]CACTCTGGAAGGCAC | 8835 |
rs144173558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93578317 | TTTAGAAAATTGTAC[C/T]CTGTTAGGAGGGTAG | 8835 |
rs144354735 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93591750 | CGGTCACAGGCTGAC[C/G]AACGTCAAGGCGTTT | 8835 |
rs144365743 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SOCS2 | GRCh38.p7 | 12:93610313 | AGGACACCCCTCAGT[C/T]CCGGGCTAACCTGGA | 8835 |
rs144372292 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93612479 | CAGGCTTCCTTTGAA[C/G]CAGTTTCATATTTTG | 8835 |
rs144422966 | in-del | -/TTTTAAAGTATACT | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93577672 | ACTGGAAAAGTATAG[-/TTTTAAAGTATACT]ATACCTTAATTAGCA | 8835 |
rs144442814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93602416 | TCAGTATTTGTAGCA[C/T]ATACATACACATGAA | 8835 |
rs144545622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SOCS2 | GRCh38.p7 | 12:93580569 | GAGGTTGCTGTGAGC[A/G]GCAATCTTACCACTG | 8835 |
rs144856913 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93570164 | CCGGACTGAGGGAAC[C/T]GAGGCCAGTCACCAA | 8835 |
rs144943515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93595009 | CCTTGACTTCCTTAC[A/G]TTTGTAAACTATGTG | 8835 |
rs144978719 | snp | A/G | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93591419 | GGAGAAAGCGTGTGT[A/G]CGTTCGTGTGTGGCT | 8835 |
rs145008057 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | SOCS2 | GRCh38.p7 | 12:93588914 | GGCGTGAGCCACCGC[A/G]CCTGGCCTGACAGAG | 8835 |
rs145045048 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SOCS2 | GRCh38.p7 | 12:93614267 | TTTCCTCCAAACACA[C/T]GATGCTCTGAGAATT | 8835 |
rs145216715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93606072 | CTCCTCCTATCTTGT[C/T]GCTCTGCTCTTCCTA | 8835 |
rs145356519 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93598044 | ATATGTAAACATTTG[A/C]ATACATGAGATAATT | 8835 |
rs145458017 | in-del | -/T | 0.230896 | 0.249269 | intron-variant | SOCS2 | GRCh38.p7 | 12:93620422 | TTCTCTTTTTTTTTT[-/T]GAGATGGAGTCTTGC | 8835 |
rs145495513 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | SOCS2 | GRCh38.p7 | 12:93613114 | CTGCAAGAAAGGGCA[A/G]TGCCAAGGAACAGAG | 8835 |
rs145496196 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93578755 | GAGTCAGGATTCAAA[C/T]GCAGATATTTTAGTC | 8835 |
rs145650183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93599753 | TATAAAAGCAAGTTT[A/G]GCTTTCTCTTGCTCT | 8835 |
rs145729749 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SOCS2 | GRCh38.p7 | 12:93595964 | ATAGAGGGCAAAAAC[A/G]GTCATAATTTTATTG | 8835 |
rs145804003 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | SOCS2 | GRCh38.p7 | 12:93622987 | AGGTTCAAAGTAGCA[A/T]GATAACTTTGCTGTT | 8835 |
rs145979802 | in-del | -/TACAGCCTAAGGCTACAGCC | 0.0410537 | 0.137264 | intron-variant | SOCS2 | GRCh38.p7 | 12:93603440 | CCCAGTCCAAGTTAG[-/TACAGCCTAAGGCTACAGCC]TACGGTTTTGACCAC | 8835 |
rs145997655 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93608075 | GTGCAATCATAACTC[A/G]CTGCAGCCTTGATCT | 8835 |
rs146000243 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SOCS2 | GRCh38.p7 | 12:93585535 | GAAATGTTTGGTGAG[C/T]GGCATGGTGTAACCA | 8835 |
rs146078801 | snp | C/T | 1.64811e-05 | 0.00287059 | synonymous-codon, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93574960 | TGTGGTTCATCTGAT[C/T]GACTACTATGTTCAG | 8835 |
rs146101613 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SOCS2 | GRCh38.p7 | 12:93584011 | CTTCATTCCATAAAA[C/T]AGAGTAAGTGTTCCA | 8835 |
rs146264056 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SOCS2 | GRCh38.p7 | 12:93620321 | GTACCAAAATTTAAA[C/T]CATTTTCTATTGTGG | 8835 |
rs146364053 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | SOCS2 | GRCh38.p7 | 12:93611929 | GTTTTCTTTACAACT[C/G]CTCCCTCTGCTCAGA | 8835 |
rs146415594 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SOCS2 | GRCh38.p7 | 12:93578353 | AGAGACGTCATCTTC[A/G]TCAAGTAATCCAAAG | 8835 |
rs146506117 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SOCS2 | GRCh38.p7 | 12:93581406 | AGGAGTGAACAATTC[A/G]AGGAATGATTTTTTT | 8835 |
rs146783218 | snp | A/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93598236 | GCCTTAACGTAAGGA[A/T]GAGTTTGGTTTGTAC | 8835 |
rs146817350 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SOCS2 | GRCh38.p7 | 12:93582678 | GGAAAGCAAGAGGTC[A/G]CGGTGCAGCGGGCAC | 8835 |
rs146914028 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | SOCS2 | GRCh38.p7 | 12:93579764 | CCTGGAGTCCCCAGT[A/G]TCTGAAGTCATGGAG | 8835 |
rs147089526 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SOCS2 | GRCh38.p7 | 12:93623273 | TGCTGCCATGTAAGA[C/T]GTGCCTTGCTTCCCC | 8835 |
rs147105938 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93618733 | TCTATGTCATTGTCT[C/G]ACTACTTTACTTTAT | 8835 |
rs147139194 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SOCS2 | GRCh38.p7 | 12:93596700 | GGGCGTGTTGGCCTG[C/T]GCCTGTAATCTCAGC | 8835 |
rs147142851 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SOCS2 | GRCh38.p7 | 12:93591649 | AGCCCCACGGAGCTG[C/T]GGCGTGGCGGCTCCT | 8835 |
rs147245149 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | SOCS2 | GRCh38.p7 | 12:93575710 | ATCCCATTTTATGCA[A/G]TTAACCAAATCAACC | 8835 |
rs147248694 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SOCS2 | GRCh38.p7 | 12:93619214 | AACGCAGGGGACAAG[C/T]GGTGACTGGGTAAGT | 8835 |
rs147265013 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SOCS2 | GRCh38.p7 | 12:93615848 | TGATCCTCCCGCCTC[A/G]GCCTCCCAAAGTGTT | 8835 |
rs147456080 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93615258 | TTTTGGTTCATTGTT[A/C]ATTCCCAGAGTCTAG | 8835 |
rs147459298 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SOCS2 | GRCh38.p7 | 12:93612883 | ATCTATTTTACTCCT[C/T]TTCATTTCCTTCCCT | 8835 |
rs147581612 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B, intron-variant | SOCS2 | GRCh38.p7 | 12:93586381 | TCAGACTTGAAGCTT[C/T]TCAGGCACATTAGAG | 8835 |
rs147715736 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SOCS2 | GRCh38.p7 | 12:93582565 | CTCAGATTTGCCCTG[A/G]AGTATGCGGCTTTGA | 8835 |
rs147731724 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SOCS2 | GRCh38.p7 | 12:93626072 | CGCCTGGGTTTTAGA[C/T]GGTTCTGCCAAAGGT | 8835 |
rs147820662 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SOCS2 | GRCh38.p7 | 12:93613323 | ATGTACAGCCTACTG[C/T]GGTCAATGCTTTATT | 8835 |
rs147833968 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SOCS2 | GRCh38.p7 | 12:93610434 | GGGGAGCCTGTGAGT[C/T]TGTATTTCTGACAAA | 8835 |
rs147895719 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SOCS2 | GRCh38.p7 | 12:93610192 | ATATGTTACAACAGT[C/T]GTTCTCAGACTTTAG | 8835 |
rs147923990 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SOCS2 | GRCh38.p7 | 12:93591892 | CTCACTAGACCGTAT[A/T]TGAGAATGTGGCCAG | 8835 |
rs147940955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93587121 | TGCAGTGTGCTGAGA[C/T]GGCACCACTGCACTC | 8835 |
rs148049774 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93596600 | TGGGAGGCTGAGGCG[G/T]GCAGATCACATGAAG | 8835 |
rs148065329 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93611323 | GCTCACTGCAACCTC[C/T]ACCTCCTTGGTTCAA | 8835 |
rs148086876 | snp | C/T | 0.000131815 | 0.00811728 | synonymous-codon, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93574885 | AATCGAATACCAAGA[C/T]GGAAAATTCAGATTG | 8835 |
rs148099131 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93583137 | TAGATGTTGGTTGTC[A/G]TGGAGAAACAGGAAT | 8835 |
rs148189635 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93568024 | GATTATATTGGATGC[C/T]TACTACATGCTAAGA | 8835 |
rs148306365 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SOCS2 | GRCh38.p7 | 12:93624014 | CAGCCTGAGCCACTG[C/T]GCCTGGTCTTAATCA | 8835 |
rs148346233 | snp | C/G/T | 3.29915e-05 | 0.00406138 | missense, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93574809 | TGATTAGAGATAGCT[C/G/T]GCATTCAGACTACCT | 8835 |
rs148353066 | in-del | -/T | 0.409721 | 0.192325 | intron-variant | SOCS2 | GRCh38.p7 | 12:93574577 | TATTTGTGGTGGCCC[-/T]GGTAAACTTTCGCTC | 8835 |
rs148362267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93618423 | GCCCTTCGAAGACTT[C/T]CTGACACTCTTAAAG | 8835 |
rs148412489 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, intron-variant, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93586176 | AAGTTTCTGAATGAC[C/T]GGAAGTTCTTCTGAT | 8835 |
rs148417678 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SOCS2 | GRCh38.p7 | 12:93602778 | TCCTGCCTCAGAGCC[C/T]TGCATTCTGTAATCC | 8835 |
rs148454919 | in-del | -/ACTT | | | intron-variant, downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93583892 | GACAAGGAGATTGAC[-/ACTT]ACACAGATTAAATGA | 8835 |
rs148482980 | in-del | -/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93603620 | TTATTACCTTTATTA[-/T]TTTTTTTAAAGCCAT | 8835 |
rs148539883 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93577291 | TCAATCTTCCATATT[A/G/T]CAAGTAGGTTGATAA | 8835 |
rs148673684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93619768 | TGCATGTTTCCATAC[C/T]TGCATCAGCCTGGAA | 8835 |
rs148802768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93612778 | ATGGTGGTAGTATCA[C/T]TGGTAATTTCTGTTT | 8835 |
rs148853656 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SOCS2 | GRCh38.p7 | 12:93578884 | TCATATATTTCTTCC[G/T]CTGGGATTCAGAAGC | 8835 |
rs148901563 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SOCS2 | GRCh38.p7 | 12:93610657 | AGAAGAGGTAGAAGG[A/G]AGTGCCCTAGTCCGT | 8835 |
rs148979676 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | SOCS2 | GRCh38.p7 | 12:93607262 | TTTTATTTGAAGGAG[-/A]AAAAAAGTAGCATTG | 8835 |
rs148989717 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SOCS2 | GRCh38.p7 | 12:93593228 | TTATCACGCTGACCC[G/T]ACTCTATATCTAGAT | 8835 |
rs149061586 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SOCS2 | GRCh38.p7 | 12:93618170 | TACCCTTTGCCTTCC[A/G]CCATGATTGTAAGTT | 8835 |
rs149111408 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93567860 | CCATGATCATCTCCA[A/G]AAGAGGCTAAATAAA | 8835 |
rs149114545 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93614309 | GAATAATCTCCTACC[A/C]TCAACTCTGGGTGTA | 8835 |
rs149128726 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | SOCS2 | GRCh38.p7 | 12:93588702 | GCTCACTGCAATCTC[C/T]ACCTCCCAGGTTCAA | 8835 |
rs149164240 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SOCS2 | GRCh38.p7 | 12:93606377 | AAGCCCAAGTTACCC[C/G]ATTCAACACATCAGA | 8835 |
rs149164949 | in-del | -/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93614616 | TTCTTTCTTTCTTTC[-/T]TTCTTTCTTTCTTTC | 8835 |
rs149242986 | in-del | -/A | 0.0422008 | 0.138995 | intron-variant | SOCS2 | GRCh38.p7 | 12:93622931 | TGGATTTTTTAAAAT[-/A]AAAAAAATCACTTTC | 8835 |
rs149290508 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SOCS2 | GRCh38.p7 | 12:93596489 | TCCTAAGATAAGACT[A/G]CCAAGAGACCCAGGC | 8835 |
rs149433302 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93583049 | TTATCCTGGTTAGAA[G/T]AATTTTGTGTTTTCT | 8835 |
rs149441024 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | SOCS2 | GRCh38.p7 | 12:93615244 | AGAGCAAGGACTTTT[C/T]TTGGTTCATTGTTCA | 8835 |
rs149480626 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SOCS2 | GRCh38.p7 | 12:93609031 | TTGGGAGGCTGAGGC[A/G]GGCAGATAACTTGAG | 8835 |
rs149504495 | in-del | -/T | 0.0792508 | 0.182605 | intron-variant | SOCS2 | GRCh38.p7 | 12:93604827 | GGCTGATATTTTTTT[-/T]CTTTTTTGTAGAGAC | 8835 |
rs149599079 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | SOCS2 | GRCh38.p7 | 12:93580382 | ATCCCAGCACTTTGG[A/G]AGGCCAAGGTGGACG | 8835 |
rs149636251 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SOCS2 | GRCh38.p7 | 12:93612289 | CTCCTGCAGTCTAGG[G/T]TGATTCCTCCATGGT | 8835 |
rs149699789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93622449 | TCATTGGCATGTCAG[C/T]TATGATGCTGCACTC | 8835 |
rs149723463 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93572830 | CACTGACTTCAAGGA[A/G]GGACGCGAACCCTTC | 8835 |
rs149758493 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93585812 | GATCCCAGGACTCCC[A/G]CCCCTGCCCCCTCAA | 8835 |
rs149927527 | in-del | -/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93608170 | TTTTTTGTTTTTTGG[-/T]TTTTTTTTTTGGTAA | 8835 |
rs149937661 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SOCS2 | GRCh38.p7 | 12:93614199 | CAGCTCAATGAATAC[C/T]TCTTATTTCTCATCT | 8835 |
rs150022874 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SOCS2 | GRCh38.p7 | 12:93597761 | GTTGTACTTCCTTTG[C/G]TGATTTATTTTAAGG | 8835 |
rs150027509 | in-del | -/CCTTTAGTAGGGCT | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93624742 | CAGAAATTGCTGGAA[-/CCTTTAGTAGGGCT]CCCATTAAGTTGCTC | 8835 |
rs150074995 | in-del | -/TC | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93574203 | GCAGGCTTTGCAGAT[-/TC]TTTTTTTTTTTTTTT | 8835 |
rs150089179 | snp | C/G | 0.0368353 | 0.130617 | intron-variant | SOCS2 | GRCh38.p7 | 12:93611356 | GATTCTCCTGCCTTA[C/G]CCTCCTGAGTAGCTG | 8835 |
rs150091226 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93578509 | TTTCTATCCTTTAGA[A/G]CAAAACAATGTTCTT | 8835 |
rs150245871 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SOCS2 | GRCh38.p7 | 12:93614918 | AGCGCCCGGCGCCTT[C/G]TATGTAGCAATTTTC | 8835 |
rs150331439 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SOCS2 | GRCh38.p7 | 12:93582504 | GTCCTTGTGAGAAGA[C/T]TGGAGAGAGAGTCAG | 8835 |
rs150347709 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | SOCS2 | GRCh38.p7 | 12:93601300 | ACTTTTTTGAGACTG[A/C]GTCTTGGTCTGTCAC | 8835 |
rs150490224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93587187 | AAAACAAAAACAAAA[A/G]ACATAGTCCCCGACC | 8835 |
rs150609135 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93609717 | GCAGTAATTTATGAC[G/T]GTTCCCTAGGGATCT | 8835 |
rs150662038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93603270 | TTACCTGGGGTCACT[A/G]TGTGCAGGGCCTTGT | 8835 |
rs150735742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93596906 | CACCTACTACAAATT[A/G]TCTTTCTTCTTGGGG | 8835 |
rs150789204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93590855 | CACATGAAAAGTACA[A/G]TCCTTTTCTTCATTT | 8835 |
rs150815945 | in-del | -/CA/CACA | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93578682 | AGATTTGCATGCTCG[-/CA/CACA]CACACACACACACAC | 8835 |
rs150825563 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | SOCS2 | GRCh38.p7 | 12:93580197 | ATCTCCCCAGTTTCC[A/G]GTTTCCTACAGTGTT | 8835 |
rs150871727 | snp | A/G | 1.68326e-05 | 0.00290104 | missense, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93575099 | AGGCTCACCATTAAC[A/G]AATGTACCGGTGCCA | 8835 |
rs150941374 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93621563 | CTCACTGCAGCCTCG[A/C]ACGGTCAGGCTTAAG | 8835 |
rs150978475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93572619 | TTCCACGTCTATTTC[C/T]CCACCCCCACCCCAG | 8835 |
rs150979726 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93607477 | TGCCAGATAAAAAGG[A/T]TACACCCCAGGAAGA | 8835 |
rs150994637 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93616364 | TCCAGTTTTCTTGGT[G/T]TGGCACTGAGGTCTC | 8835 |
rs151051051 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SOCS2 | GRCh38.p7 | 12:93599878 | TTCCCAGCCCATAGA[A/C]GTGTGAGAAATAAAA | 8835 |
rs151108470 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | SOCS2 | GRCh38.p7 | 12:93593704 | TGGAAAATAACCCTA[C/G]TAAGACCAAGCCCAC | 8835 |
rs151157585 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SOCS2 | GRCh38.p7 | 12:93625363 | TTTCTAGTTCATGCA[A/G]TTGAAATAAAGGTAC | 8835 |
rs151229303 | in-del | -/TA | 0.0644693 | 0.167566 | intron-variant | SOCS2 | GRCh38.p7 | 12:93584276 | GGGAAATTAGGCTGT[-/TA]TACCTCTCTCCCGAT | 8835 |
rs180744847 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SOCS2 | GRCh38.p7 | 12:93581475 | GTCTTCTACTATGGA[G/T]CAGGCCATCTCCTGA | 8835 |
rs180800407 | snp | A/G | 0.000783853 | 0.0197816 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93571903 | GCGGCGGCGGCCGCG[A/G]CCGAGGTCGAGGTAA | 8835 |
rs180801187 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SOCS2 | GRCh38.p7 | 12:93600831 | TCTTGATCTGTCACC[C/T]GGGCTGGAGTGCAGT | 8835 |
rs180808314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93613079 | CCGGCACTTCTTTCT[A/G]TCAGAGCCTGTGTGG | 8835 |
rs180822478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93619201 | CCACAGCCATGGCAA[C/T]GCAGGGGACAAGCGG | 8835 |
rs180837443 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93591762 | GACCAACGTCAAGGC[A/G/T]TTTCACTTTGGAAGC | 8835 |
rs180988691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93588000 | AGGCTGCTCTGGAGG[A/G]ACGTGACCTGAGATC | 8835 |
rs181008316 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93607430 | AGGGAACCTGGTTCC[C/T]GAGAGTTCACATTTG | 8835 |
rs181045684 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93615411 | ACATTCCTGGGCAGG[G/T]ATCCTGCAGAGTAGA | 8835 |
rs181068817 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | SOCS2 | GRCh38.p7 | 12:93576138 | ACCTGCCTGTTTTTC[A/G]AAGTGTTTATTTACT | 8835 |
rs181078453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93595829 | AACAAAATGAGCTGT[C/T]TTATTTTATTTTACT | 8835 |
rs181281918 | snp | C/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93604999 | GATTGCTCACATGTA[C/T]AGGGTAAAATTTTTA | 8835 |
rs181296701 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SOCS2 | GRCh38.p7 | 12:93623765 | ACGCAGGAGTGCAAT[C/T]GCGATCTCAGCTCAC | 8835 |
rs181297021 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93577334 | AATTATTTTTGGTTT[G/T]GTTTTGTTTTTTTAC | 8835 |
rs181308881 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SOCS2 | GRCh38.p7 | 12:93587092 | AGAATCACTTGAACC[C/T]GGGAGGCAGAGGTTG | 8835 |
rs181343443 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SOCS2 | GRCh38.p7 | 12:93615750 | ACAGGCATGAGCCAC[C/G]ATGTTCAGCTAATTT | 8835 |
rs181387717 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93596895 | GCACCCTCCACCACC[A/T]ACTACAAATTGTCTT | 8835 |
rs181410940 | snp | A/T | 7.25452e-05 | 0.00602224 | utr-variant-3-prime, intron-variant | SOCS2 | GRCh38.p7 | 12:93575195 | ATGTTTCTCTTTTTT[A/T]AAACATGTCTCACAT | 8835 |
rs181669451 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SOCS2 | GRCh38.p7 | 12:93605348 | GATACTTATACTTCT[G/T]AAGACATAAATACAC | 8835 |
rs181727336 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SOCS2 | GRCh38.p7 | 12:93601197 | TCATTTGTATCCAGC[A/G]ACCTTTCTGAATTCT | 8835 |
rs181733451 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93620395 | TGTCCTGAAGAGTTT[G/T]GAGCTACATTTCTTT | 8835 |
rs181744436 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93625216 | CTATCCTCACCAGTT[A/C]TTTTATTTATTTGTT | 8835 |
rs181757708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93582091 | GTGTAGTTACTTTGC[A/G]GACAGGGTGCCATTG | 8835 |
rs181762034 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SOCS2 | GRCh38.p7 | 12:93587758 | GCAGACCACACGAAG[G/T]TGTGAGAGAACACAG | 8835 |
rs181776024 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SOCS2 | GRCh38.p7 | 12:93624504 | TTGAATCCGGGAGGC[A/G]GAGGTTGTAGTGAGC | 8835 |
rs181780340 | snp | A/G | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93601561 | TGATCTGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 8835 |
rs181876817 | snp | G/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93591398 | GAATGAACAAGATGG[G/T]AGCGAGGAGAAAGCG | 8835 |
rs181886616 | snp | A/C | | | intron-variant, upstream-variant-2KB | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93570845 | GAAGCCTGTGTATTG[A/C]GACCGAGCCTCTTTA | 8835 |
rs181890970 | snp | A/G | 0 | 0 | intron-variant | SOCS2 | GRCh38.p7 | 12:93612011 | TGAATTCTCAGTCAG[A/G]CCTTGTCATTTCTGG | 8835 |
rs181898535 | snp | C/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93591335 | TACATATACAAGGAA[C/T]GGAAATGAATTAGCC | 8835 |
rs182093344 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93569304 | GGCAGTTAACCCTAG[C/T]AGACATAGTGGTTCT | 8835 |
rs182124305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93584394 | GGTCTAGTGCAAGAC[C/T]TTAGTCCAAAACAAT | 8835 |
rs182131860 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | SOCS2 | GRCh38.p7 | 12:93621655 | CTAATTAAAAAAAAA[A/T]TTTTTTTTTGTAGAG | 8835 |
rs182135351 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SOCS2 | GRCh38.p7 | 12:93602216 | TTCTGCCTCAGCTTA[C/T]CCTAGACTACAGGTG | 8835 |
rs182189720 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SOCS2 | GRCh38.p7 | 12:93611385 | TGGGATTGCAGGTGT[G/T]TGCCACCACGCCCGG | 8835 |
rs182372716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93622646 | GCTTCTATGCCAATA[C/T]TCTGGTTGGAAGAAA | 8835 |
rs182394141 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SOCS2 | GRCh38.p7 | 12:93602534 | TCACATGTACTCCAG[C/G]AAATGGAACCAGTTT | 8835 |
rs182571016 | snp | C/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93614210 | ATACTTCTTATTTCT[C/T]ATCTGCCTAAGGCAG | 8835 |
rs182574649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93599267 | CAAGCAATCCTCCTG[C/T]CCCAGCCTCCCAAGT | 8835 |
rs182578248 | snp | A/G | | | intron-variant, utr-variant-3-prime | SOCS2 | GRCh38.p7 | 12:93580134 | CCATGGTGGGGTGAG[A/G]CTTTTTCGCCAGTTA | 8835 |
rs182581950 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | SOCS2 | GRCh38.p7 | 12:93626209 | TGTACTCCTTGAAGG[C/T]TTCTTAAGGTAATGT | 8835 |
rs182583588 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93617811 | TCAAATCCATTTACA[C/T]CTCTCCACTTCCACT | 8835 |
rs182951773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93597596 | GCTGAGATTACAGGT[A/G]TGAGCCGCCATGCCC | 8835 |
rs182983382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93578352 | CAGAGACGTCATCTT[C/T]GTCAAGTAATCCAAA | 8835 |
rs183012982 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93578907 | TCAGAAGCCAGGCCT[G/T]TGGAATACCCTGTGG | 8835 |
rs183088250 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93585887 | TATATGAAACGGTAT[A/G]GTATTTGCATATAAC | 8835 |
rs183104698 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93588714 | CTCCACCTCCCAGGT[G/T]CAAGCAATTCTCCTG | 8835 |
rs183107953 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93613216 | AAGAGCCTTTTAAAA[C/G]AACAAAGCTTCTGTA | 8835 |
rs183168995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93573224 | AAAGTGGTTCTCCAG[A/G]GACTCAGGCCTGGCG | 8835 |
rs183363698 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93608088 | TCGCTGCAGCCTTGA[G/T]CTCCTGAGCTCAAGT | 8835 |
rs183414515 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SOCS2 | GRCh38.p7 | 12:93613426 | AAAAAAACCAAAAAC[A/C]AAAACAAACAAACAA | 8835 |
rs183416076 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SOCS2 | GRCh38.p7 | 12:93609077 | CCAGCCTGGGCAACA[C/T]GGTGACACCCTGTCT | 8835 |
rs183443661 | snp | C/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93592703 | ATTTTCCATTGAGAT[C/T]GAATAAACTTGTTTA | 8835 |
rs183475671 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SOCS2 | GRCh38.p7 | 12:93573558 | GCCGAGCGCGGCTTC[C/T]ATGGTCGGCGCGCCC | 8835 |
rs183586127 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SOCS2 | GRCh38.p7 | 12:93590025 | TTGGGAGGCCAAGGT[A/G]AGCGGATCATGAGGT | 8835 |
rs183606854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93592365 | TGATATGAATGTACC[A/G]TTACTGATTGAATCA | 8835 |
rs183650910 | snp | G/T | 0.000798403 | 0.0199641 | downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93626553 | AACCCCCCTACAGCC[G/T]TCTTACCTTTCCAAA | 8835 |
rs183662322 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | SOCS2 | GRCh38.p7 | 12:93598166 | AAACACGTTGCTGAC[A/G/T]ATACTGTGTTTTCGA | 8835 |
rs183747618 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SOCS2 | GRCh38.p7 | 12:93604785 | CCTCCTCAGCCCCCA[A/T]CGTAGCTGGGATACA | 8835 |
rs183755321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93623461 | ACTTTACGTTTTAGG[A/G]TACATGTGCACAATG | 8835 |
rs183772152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93586974 | GGAGTTCAAGACCAG[C/T]CTGGCCAACATGGCA | 8835 |
rs183807394 | snp | C/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93593749 | CATCTTAAATGAAGC[C/T]AAGTCAAGTCAGAAT | 8835 |
rs183809895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93574379 | ATCTTTATTTTACTT[A/G]AATAATGTTAAAAGT | 8835 |
rs183904220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93617180 | GTTCTTCATTACCAG[A/G]TGCAATAAGCAGGAA | 8835 |
rs183965862 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | SOCS2 | GRCh38.p7 | 12:93583408 | CAATTAAGAAAAAAG[A/T]AAAGGAAACAAAAAA | 8835 |
rs183991817 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SOCS2 | GRCh38.p7 | 12:93621051 | TGAAGATGTAACATT[C/T]CACCATCTTCAGTGC | 8835 |
rs184067939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93623766 | CGCAGGAGTGCAATC[A/G]CGATCTCAGCTCACT | 8835 |
rs184124890 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SOCS2 | GRCh38.p7 | 12:93601624 | AAAGTCTGGATTTTT[A/T]AAATGTATTTGTTCA | 8835 |
rs184294504 | snp | G/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93591337 | CATATACAAGGAACG[G/T]AAATGAATTAGCCCG | 8835 |
rs184296066 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93618743 | TGTCTCACTACTTTA[C/G]TTTATTTTCTTCACT | 8835 |
rs184315778 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | SOCS2 | GRCh38.p7 | 12:93580396 | GGAGGCCAAGGTGGA[C/T]GGATCACTTGAGGTC | 8835 |
rs184320621 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93570624 | AGGCCAAGGGCCAAG[C/G]ATCGCTATCCTTCCC | 8835 |
rs184330788 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SOCS2 | GRCh38.p7 | 12:93599634 | ACAGTGTTGAGGAGA[A/G]GTGGGACCTTTAATA | 8835 |
rs184455886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93593386 | TAAGAAAAGCAAACA[A/G]ATAGGGCTCAGCCTG | 8835 |
rs184627349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93605152 | TATTTCAAATATACA[A/G]AAAGCACAGAGCACA | 8835 |
rs184724503 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93609953 | AGGGCAAGAGAGAAC[A/C]AGAAAGCAAGAAGGG | 8835 |
rs184756579 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SOCS2 | GRCh38.p7 | 12:93590123 | CTGGTGTGGTGGTGC[A/G]CGCCTATAATCTCAG | 8835 |
rs184762840 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93567828 | TTAATTCTCACAACA[G/T]CCCTGTAAGGTAGGG | 8835 |
rs184776729 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SOCS2 | GRCh38.p7 | 12:93587103 | AACCCGGGAGGCAGA[A/G]GTTGCAGTGTGCTGA | 8835 |
rs184818381 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SOCS2 | GRCh38.p7 | 12:93575458 | GTAAAGGCTGAAGTC[A/G]CGTTTTATCAGAATG | 8835 |
rs184823339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93614860 | CTCAGGTGATCCATC[C/T]GCCTCGGCCTCCCAA | 8835 |
rs184826337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93595536 | TGGAATGCTTTTCTT[C/T]GGCCAACTGAAAGTA | 8835 |
rs184913569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93590934 | GAGAGTGATTACCTG[A/G]TAATATGATGAGTTA | 8835 |
rs184951054 | snp | C/G | | | upstream-variant-2KB, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93568698 | TGGGATTACAGGCGT[C/G]AGCCACCGCGCCCGG | 8835 |
rs185013098 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SOCS2 | GRCh38.p7 | 12:93611054 | TAACTCTCATTTTAT[A/G]AATCTTCAAGGAGGT | 8835 |
rs185086530 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SOCS2 | GRCh38.p7 | 12:93625708 | AGCTGAGATCACGCC[A/G]CTGCACTCCAGCCTG | 8835 |
rs185102903 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SOCS2 | GRCh38.p7 | 12:93588002 | GCTGCTCTGGAGGGA[C/T]GTGACCTGAGATCAG | 8835 |
rs185143121 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SOCS2 | GRCh38.p7 | 12:93611395 | GGTGTGTGCCACCAC[A/G]CCCGGCTAATTTTTG | 8835 |
rs185384727 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93600133 | TAGTTGTTGAATTCA[C/G]CTGAAAAAAAAATTA | 8835 |
rs185511990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93580725 | TTCCCCCTTGCCATC[C/T]TGATGAACTTGACCC | 8835 |
rs185559454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93615914 | AGTGTGAAAGTAGAA[A/G]GGACCTTAGAGGTTA | 8835 |
rs185573264 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93619108 | AAAGCTATCCCCACC[A/G]GTAGAACTGAAGGGG | 8835 |
rs185597426 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93597380 | TTGCCCAGGCATGAT[A/C]TCAGCTCACTGCAAA | 8835 |
rs185601478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93577772 | GCTCATAATGACTGC[C/T]GTGCAGGTGGGCGGG | 8835 |
rs185622448 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93586177 | AGTTTCTGAATGACC[A/G]GAAGTTCTTCTGATC | 8835 |
rs185680156 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SOCS2 | GRCh38.p7 | 12:93623098 | CCCAAGTCTCATCTC[A/G]AATTGTAACCCCCAA | 8835 |
rs185752400 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93603688 | CCTTTTTTACAGAGA[A/G]ACCCGGTATTTTTCC | 8835 |
rs185802106 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SOCS2 | GRCh38.p7 | 12:93619368 | GAACAGGGCAGGAAG[C/G]GTGGGGCACAGGGCA | 8835 |
rs185804571 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93600930 | AGTAGCTGGGACTAC[A/G]ATTGTGCATCACCAC | 8835 |
rs185842146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93581555 | ATTTCTTAGTAGGAA[A/G]GTGTTAGGCAATCTC | 8835 |
rs185904888 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SOCS2 | GRCh38.p7 | 12:93576406 | GCATTGTCAAGTGGC[C/T]GGGTCTTTTATAATT | 8835 |
rs185990981 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93615561 | CAGCATATAATTTAC[A/C]AGGGATATTAGGTGG | 8835 |
rs186049514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93596122 | GAATCCTTGGGATCA[A/G]TAATAGACATATTTG | 8835 |
rs186136499 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93591556 | GTGCACACACTGTCT[C/T]TCAAGAGGGAAGTGA | 8835 |
rs186138939 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SOCS2 | GRCh38.p7 | 12:93620485 | CAGTGGCACGATCTC[A/G]ACTCACTGCAACCTC | 8835 |
rs186142469 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93571167 | GCGCCGGGGTCCCGG[G/T]TGCACAGCCTCAGGA | 8835 |
rs186146766 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SOCS2 | GRCh38.p7 | 12:93612141 | GCAAAATAAAAGGAT[G/T]TATCTAAACTGCTAA | 8835 |
rs186484950 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93591863 | TTTTAATCTTTTCAC[G/T]TAGTCTTAAGGGTCT | 8835 |
rs186564713 | snp | A/T | 5.01651e-05 | 0.005008 | missense, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93575090 | CATCTCTGTAGGCTC[A/T]CCATTAACAAATGTA | 8835 |
rs186587760 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | SOCS2 | GRCh38.p7 | 12:93597637 | CTCGCTTTTAAAAAA[A/T]AATTTTTTGTATTAT | 8835 |
rs186594005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93616588 | ACCAAACCACATCGG[A/G]CATTCCTCTGATTAA | 8835 |
rs186664738 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93572203 | TTGGTGCCTCGGGGC[C/T]CCGCAGCGCTTTAGG | 8835 |
rs186715377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93582446 | GGAACAAAGCAAGGG[C/T]GGAGAGAGGGAGACC | 8835 |
rs186746800 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | SOCS2 | GRCh38.p7 | 12:93613087 | TCTTTCTATCAGAGC[C/G]TGTGTGGAGCCCTGC | 8835 |
rs186806156 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SOCS2 | GRCh38.p7 | 12:93590222 | ACTGGGTGACAGAGC[A/G]AGACTCAGTCTCAAA | 8835 |
rs186811694 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93568029 | TATTGGATGCCTACT[A/G]CATGCTAAGAACTAT | 8835 |
rs186866498 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | SOCS2 | GRCh38.p7 | 12:93610849 | CCTCTGAAACTATGA[A/C/G]CAATGAATTTCTGTT | 8835 |
rs186946744 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | SOCS2 | GRCh38.p7 | 12:93580242 | GTTTGTTTTTGCTAA[A/G]CATTTTTTCCCTTCT | 8835 |
rs186954080 | snp | C/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93618123 | TCCCACTCTCTCTTC[C/T]GCCTGCTCTGGCCAT | 8835 |
rs186958231 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SOCS2 | GRCh38.p7 | 12:93599493 | GTTATAGGATTTCTT[C/T]ACATATTCCAGGTAA | 8835 |
rs186996732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93601436 | CCCACCACCATGGCC[A/G]GCTTTTCAGTAGAGA | 8835 |
rs187036743 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SOCS2 | GRCh38.p7 | 12:93601837 | ACTGTCTTTTTTTTA[C/T]TCCTGCTTCCTATTC | 8835 |
rs187162281 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93621752 | GCCTTCCAAAGTGAG[G/T]GCTAGGACTATAAGC | 8835 |
rs187177303 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93584874 | TTCAAGTGATTCTCT[C/T]GCCTCAGCCTCCCGA | 8835 |
rs187192175 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SOCS2 | GRCh38.p7 | 12:93602455 | ATATGAATGTATGTG[C/T]ATGTATAAAGTCATG | 8835 |
rs187242297 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93583557 | TAAAGTGGGGCACAT[A/C]TCTGGTCTTGATAGT | 8835 |
rs187243708 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93621547 | AGTGGAACAATCATA[G/T]CTCACTGCAGCCTCG | 8835 |
rs187319071 | snp | C/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93587782 | AACACAGTTTGTTCC[C/T]ATAAGTTCTACCACT | 8835 |
rs187325084 | snp | A/G | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93624629 | TGTTTTGTTATAGCA[A/G]CACAAACAGACTAAG | 8835 |
rs187523757 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93613223 | TTTTAAAACAACAAA[G/T]CTTCTGTATAAATAG | 8835 |
rs187543773 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SOCS2 | GRCh38.p7 | 12:93592556 | CTTAACATTTTAATA[G/T]ATATTTACTTTCAAA | 8835 |
rs187551291 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93573272 | AGAGCTTCTTGGAAA[C/T]AGCTTCTTAGCACGC | 8835 |
rs187593155 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SOCS2 | GRCh38.p7 | 12:93578756 | AGTCAGGATTCAAAC[A/G]CAGATATTTTAGTCT | 8835 |
rs187594825 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93606313 | ATTGAGGGCCACTAG[A/G]AGTGCCACAAGTGGA | 8835 |
rs187602795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SOCS2 | GRCh38.p7 | 12:93579953 | TCCTTAACTTATAGG[C/T]ATTCTGACTTGCCCT | 8835 |
rs187613309 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SOCS2 | GRCh38.p7 | 12:93617625 | TCCACTCTAAAGTGG[C/T]CATACAGATACTCCA | 8835 |
rs187826089 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SOCS2 | GRCh38.p7 | 12:93613941 | AAAAAAGAATAGAAC[A/G]CACTTCAAAGCCAAG | 8835 |
rs187831951 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93592723 | AAACTTGTTTATTTG[C/T]TAATTAATTGCCCTT | 8835 |
rs187849898 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SOCS2 | GRCh38.p7 | 12:93608695 | TATTTCTGACAATGC[A/G]ATGTCTTATTTATTG | 8835 |
rs187867028 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SOCS2 | GRCh38.p7 | 12:93598647 | ACTTATGTTGATACT[C/T]TTAGATAAAGTTAAC | 8835 |
rs188081013 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SOCS2 | GRCh38.p7 | 12:93590033 | CCAAGGTGAGCGGAT[C/G]ATGAGGTCAGGAGTT | 8835 |
rs188123520 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | SOCS2 | GRCh38.p7 | 12:93604920 | CCTGCCTTGGCCCCC[C/G]CAAAGTGCTAGGATT | 8835 |
rs188132833 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SOCS2 | GRCh38.p7 | 12:93593435 | GACCTTGATTTACAT[A/G]TACAAGGAACAGAAA | 8835 |
rs188135613 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SOCS2 | GRCh38.p7 | 12:93623752 | CGCTCTGCTGCCCAC[A/G]CAGGAGTGCAATCGC | 8835 |
rs188138199 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SOCS2 | GRCh38.p7 | 12:93589072 | CTATCATTATTTACC[A/G]TACAGCATGGTTTAA | 8835 |
rs188190254 | snp | A/C | | | downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93626346 | GGCCTCCCTCTACCC[A/C]CACTGCAACCTCCCA | 8835 |
rs188379690 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93586074 | CCCCCAAATATTTTC[A/G]TTCTGTGGTTGGTTG | 8835 |
rs188434955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93614318 | CCTACCCTCAACTCT[A/G]GGTGTATAGGGATTC | 8835 |
rs188452061 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93574178 | CTTTCTACATAGAAG[G/T]CTGTTCATAGCAGGC | 8835 |
rs188462240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93622942 | AAAATAAAAAAATCA[C/T]TTTCAGTTCTTAAAA | 8835 |
rs188594822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93581682 | TTTTTTTTTCTTCCT[C/T]CCTCCCTTCTCACCT | 8835 |
rs188647224 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SOCS2 | GRCh38.p7 | 12:93573864 | GGTAATTGTGGGGGT[A/G]GGGGGAGCACAAATG | 8835 |
rs188657098 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SOCS2 | GRCh38.p7 | 12:93619745 | CTTGCATTACACTAA[A/G]CATATATTGCATGTT | 8835 |
rs188663383 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | SOCS2 | GRCh38.p7 | 12:93600951 | GCATCACCACACCTG[A/T]CTAATTTTTTTAAAT | 8835 |
rs188672547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93603463 | AAGGCTACAGCCTAC[A/G]GTTTTGACCACTTCT | 8835 |
rs188683487 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SOCS2 | GRCh38.p7 | 12:93604466 | TACAATAAAAATGTA[A/G]TTTTGTCAGAAGAAT | 8835 |
rs188774296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93591366 | CGGCTAGATATTTCT[A/G]GGAACTAGTTAAGGG | 8835 |
rs188776535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93618815 | ATAAGCCCCATAAGG[A/G]CAAGGATGTTGTCTA | 8835 |
rs188780298 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93570664 | GCGCTCAGCTGGCCC[A/G]GGTAGGGGGCAGGCT | 8835 |
rs188790609 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93611561 | TGTTTGCTTTGCAGA[C/T]GGCATTATTTCAACA | 8835 |
rs188836644 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SOCS2 | GRCh38.p7 | 12:93586994 | CCAACATGGCAAAAC[C/T]CTGTTTCTACTAAAA | 8835 |
rs188959795 | snp | A/C | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93623108 | ATCTCGAATTGTAAC[A/C]CCCAAATGTCAGGGA | 8835 |
rs189012820 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SOCS2 | GRCh38.p7 | 12:93596701 | GGCGTGTTGGCCTGC[A/G]CCTGTAATCTCAGCT | 8835 |
rs189015752 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93595224 | TTATTTTACTGAGTT[C/G]CACACTGATAGTTAA | 8835 |
rs189024001 | snp | C/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93614500 | TTCCTTCCTTCCTTC[C/T]TTCCTTCCTTCCTTC | 8835 |
rs189218963 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SOCS2 | GRCh38.p7 | 12:93609819 | ATACCACAAACTAGG[A/G]TCATTTATAAAGAAA | 8835 |
rs189221589 | snp | A/G | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93619160 | GGAGATGGTAAGAGC[A/G]GAGGCTATGGGAGAG | 8835 |
rs189267107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93615727 | CAACCTCTGAAGTAG[C/T]TGGAATTACAGGCAT | 8835 |
rs189271805 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93581419 | TCAAGGAATGATTTT[A/T]TTTTTTTTTAATGTG | 8835 |
rs189306193 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SOCS2 | GRCh38.p7 | 12:93576460 | CTCTGTGTTTCCAAA[A/C]ACATGGTTTAGAAAC | 8835 |
rs189307678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93615108 | CTTAACCCTCTCCCC[C/T]ACTGGGATAGGTGCC | 8835 |
rs189412722 | snp | A/C | 0.0103295 | 0.0711199 | utr-variant-3-prime, intron-variant, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93586204 | GATCTTCACAAACAT[A/C]TCTTGGGTTTTCTCA | 8835 |
rs189491605 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93611270 | GGAGACGGAGTCTCA[A/C]TTTGCCACCCAGGCT | 8835 |
rs189510838 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93568945 | CGAGGCAGGAGGATC[A/G]GTTGAACCCAGGAGT | 8835 |
rs189523255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93588294 | AAACTGAAATTATTA[C/T]AGATATTAGACTCAC | 8835 |
rs189533746 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SOCS2 | GRCh38.p7 | 12:93607506 | GAAGAACACAAGATA[C/T]CTGCTGTAGCCCTCT | 8835 |
rs189547615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93600412 | ACTTTGCTATCTAGT[A/G]TGGTGAGTGGTTTTT | 8835 |
rs189602365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93626156 | AGTAAAATGAGCCTC[C/T]TTCTATTTATCCCAC | 8835 |
rs189754773 | snp | A/T | 0.0298908 | 0.118541 | intron-variant | SOCS2 | GRCh38.p7 | 12:93591242 | AGGGAGGTGTTTTTT[A/T]AAAAAAAAACAAACG | 8835 |
rs189779946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93612165 | CTGCTAAACATGAGA[C/T]CTGCCCATTTTGCAC | 8835 |
rs189784240 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93591749 | CCGGTCACAGGCTGA[A/C]CAACGTCAAGGCGTT | 8835 |
rs189844676 | snp | A/G | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93584044 | TAGCTAAGCAGAAGA[A/G]GTTGGTTTTACAGCC | 8835 |
rs190049232 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SOCS2 | GRCh38.p7 | 12:93587537 | ATACAAAAAAGTAGC[C/T]GGGCGTGGTGGCACG | 8835 |
rs190051488 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SOCS2 | GRCh38.p7 | 12:93624454 | GCAGGCACCTGTAGT[C/T]CCAGCTACTAGGGAG | 8835 |
rs190138409 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93622379 | GAGGCACAAAAGTGT[G/T]GTCGGAGACTCTTGC | 8835 |
rs190289432 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant | SOCS2 | GRCh38.p7 | 12:93576008 | TTGATTTTTTGGAAA[C/T]GGCTTTAGAAATATC | 8835 |
rs190294959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93605182 | AGTAATTACCAATGC[C/T]ACCACCACCACCCAC | 8835 |
rs190457107 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SOCS2 | GRCh38.p7 | 12:93592635 | TTCTGTCTTTCAAGT[C/T]GTACACATAGCTGAG | 8835 |
rs190466108 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93573329 | GCTCAGGGTTAGGCT[C/G]CCGGGCTCGAACCCC | 8835 |
rs190517700 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SOCS2 | GRCh38.p7 | 12:93613424 | AAAAAAAAACCAAAA[A/C]CAAAAACAAACAAAC | 8835 |
rs190550232 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93599891 | GAAGTGTGAGAAATA[A/C]AATTCTTCATATGTT | 8835 |
rs190559968 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93595620 | TCAGTTAGTTCATGA[C/T]CAAAAGAAAAGACGT | 8835 |
rs190706947 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SOCS2 | GRCh38.p7 | 12:93578348 | GAGACAGAGACGTCA[C/T]CTTCGTCAAGTAATC | 8835 |
rs190764564 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SOCS2 | GRCh38.p7 | 12:93616210 | TGAGACATGATTTCA[A/G]GACATTGGAAAGAGA | 8835 |
rs190768637 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93597542 | GCTGGTCTCAAACTC[A/G]TGACCTCAAGCGATC | 8835 |
rs190786178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SOCS2 | GRCh38.p7 | 12:93580438 | CCAGCCTGGCCAACA[C/T]GGCGAAACCACATCT | 8835 |
rs190869962 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93587960 | GAACAACAGAGTGAC[C/T]GCATCAGATTTGGTG | 8835 |
rs190886222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93606845 | TTTAGTAGAAATGGG[A/G]CTTTGCCATGTTGGT | 8835 |
rs190920030 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | SOCS2 | GRCh38.p7 | 12:93621562 | GCTCACTGCAGCCTC[A/C/G]AACGGTCAGGCTTAA | 8835 |
rs191034992 | snp | A/G | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93590517 | AAGTTAGCTTCCCGT[A/G]TGGGCGTGGTGGCTC | 8835 |
rs191138640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93613179 | GCTTTCCGAAGGTAT[C/T]TTCTCCTTTTGAATG | 8835 |
rs191158863 | snp | A/C | 0.000647249 | 0.0179779 | intron-variant, upstream-variant-2KB | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93573089 | GCGCCTCCCCAAGGA[A/C]GCAGCTAGGAAGCGG | 8835 |
rs191168842 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SOCS2 | GRCh38.p7 | 12:93579962 | TATAGGCATTCTGAC[C/G/T]TGCCCTAGATCAGAA | 8835 |
rs191173360 | snp | A/G | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93602046 | ATTACAGATTGCAAG[A/G]TGGGGCCAAGAAAAA | 8835 |
rs191280857 | snp | A/C | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93611012 | GAACTCCACAGGGTT[A/C]CTTACATCCCTAGGA | 8835 |
rs191383438 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SOCS2 | GRCh38.p7 | 12:93601460 | GTAGAGACTGGGTTT[C/T]ATCATGTTGGCCAGG | 8835 |
rs191412965 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | SOCS2 | GRCh38.p7 | 12:93591887 | AGGGTCTCACTAGAC[C/G]GTATATGAGAATGTG | 8835 |
rs191530183 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93613944 | AAAGAATAGAACACA[C/T]TTCAAAGCCAAGTAT | 8835 |
rs191541749 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, intron-variant, nc-transcript-variant | SOCS2 | GRCh38.p7 | 12:93586268 | TCAATATTCAAGATA[A/G]ATAAATTATGTTCAC | 8835 |
rs191600267 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SOCS2 | GRCh38.p7 | 12:93604630 | GTTCAGAATTTTTGC[A/G]TGTTGGGTTTTTTCT | 8835 |
rs191634484 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93584949 | TGTATTTTTTGTAGA[A/G]ACAGCGTTTCACCAT | 8835 |
rs191650348 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SOCS2 | GRCh38.p7 | 12:93620627 | CCATGTTGGCCAGGC[C/T]GGTCTCAAACTCCTG | 8835 |
rs191651346 | snp | C/G | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93602530 | CTGTTCACATGTACT[C/G]CAGGAAATGGAACCA | 8835 |
rs191693263 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | SOCS2 | GRCh38.p7 | 12:93626501 | CTGGAGAACCCCTAC[A/G]TATCCTTCAAGACTC | 8835 |
rs191942441 | snp | C/T | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93616895 | CGATTAATGAAAAAA[C/T]CTTTTGGTCTGGACC | 8835 |
rs191949382 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SOCS2 | GRCh38.p7 | 12:93614609 | TCTTTCTTTCTTTCT[C/T]TCTTTCTTTCTTTCT | 8835 |
rs191951405 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SOCS2 | GRCh38.p7 | 12:93595235 | AGTTCCACACTGATA[C/G]TTAACTTTAGGAAAT | 8835 |
rs191957587 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SOCS2 | GRCh38.p7 | 12:93578770 | CGCAGATATTTTAGT[C/T]TTAGGATTACTATTT | 8835 |
rs191988786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93608790 | GGGATGCATCCCACT[C/T]GGTGCAACATCAGTT | 8835 |
rs192204869 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SOCS2 | GRCh38.p7 | 12:93580290 | TTTCCTGTTTAGTGT[A/T]TGGTCCAGAATGCTG | 8835 |
rs192205644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93598721 | AACAAATTTTCTTTA[C/T]CTATTAATTTACTTA | 8835 |
rs192218739 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | SOCS2, SOCS2-AS1 | GRCh38.p7 | 12:93568394 | GAATTAGCAAGGAGT[C/T]CAGTGTAACTTGAAC | 8835 |
rs192219516 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93618333 | ACTAAGACACCAACC[A/C]AGTAGAAAATCAGAA | 8835 |
rs192221339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93599599 | TTTGAATGTATCCCC[C/T]AGAGTTAATCCCCAG | 8835 |
rs192249057 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SOCS2 | GRCh38.p7 | 12:93597738 | GATAGCCAGATTTAA[C/T]AAATATTGTTGTACT | 8835 |
rs192283731 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93625134 | ATTTCCCATGCTGAA[A/T]CATTCACTGACTATC | 8835 |
rs192426144 | snp | C/G | | | intron-variant | SOCS2 | GRCh38.p7 | 12:93592803 | GGCCTCAACAACTTC[C/G]TCCCAGCCTTGATCA | 8835 |
rs192495752 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | SOCS2 | GRCh38.p7 | 12:93590115 | AAATTGGCCTGGTGT[A/G]GTGGTGCGCGCCTAT | 8835 |
rs192504252 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93623286 | GACGTGCCTTGCTTC[C/G]CCTTCACCTGCAGCC | 8835 |
rs192547424 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SOCS2 | GRCh38.p7 | 12:93609929 | TATCATCCCATGGTG[A/G]AAGGTGGAAGGGCAA | 8835 |
rs192585964 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93590381 | TTTCCAATAACATTT[A/C]TCAATCTGGTAACCA | 8835 |
rs192618436 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93617633 | AAAGTGGCCATACAG[A/T]TACTCCACATATTTA | 8835 |
rs192680776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93574271 | AAAGTTGCTTCTGTT[C/T]TTACTGTAGTTCAAT | 8835 |
rs192785715 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SOCS2 | GRCh38.p7 | 12:93574074 | CACTTGGGAATTCCC[A/C]TTTCTTAGTGACTGG | 8835 |