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 |