SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs10765 | snp | A/C | 0 | 0 | utr-variant-3-prime, intron-variant | SH3PXD2B | GRCh38.p7 | 5:172333669 | AAAGGAAACAAAAAC[A/C]ACCACCGGAATGCCA | 285590 |
rs12033 | snp | C/T | 0.431177 | 0.172264 | utr-variant-3-prime, intron-variant | SH3PXD2B | GRCh38.p7 | 5:172333565 | ATATACTTTACCATT[C/T]GACTTCTTTCCTTTT | 285590 |
rs867699 | snp | A/T | 0.472429 | 0.114129 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172418515 | AGTTACTTCTGAAAA[A/T]ACCAGGGCTGCTTGC | 285590 |
rs869366 | snp | A/G | 0.494442 | 0.0524218 | utr-variant-3-prime, intron-variant | SH3PXD2B | GRCh38.p7 | 5:172336858 | AGGGCAGATGTGGTC[A/G]TCTGTCAAACTGAGG | 285590 |
rs869367 | snp | A/G | 0.432797 | 0.170544 | utr-variant-3-prime, intron-variant | SH3PXD2B | GRCh38.p7 | 5:172337116 | GGGTCCTGGTGGTTG[A/G]CACAGAGCCCTGTTC | 285590 |
rs871573 | snp | G/T | 0.492918 | 0.0590819 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172419262 | ATGTCGAGGCACGCG[G/T]CCAGGCCCTGTGCAA | 285590 |
rs871574 | snp | A/G | 0.478104 | 0.102316 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172419340 | ATCTGGAAGAGATTT[A/G]ATGAGAAGCGGAGTG | 285590 |
rs876924 | snp | A/G | 0.491421 | 0.0649309 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172435915 | GCTAATGGACCACAG[A/G]GTTCTGTCTTGCGGA | 285590 |
rs876925 | snp | C/G | 0.434253 | 0.168969 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172435705 | tgtgcgtgatggctc[C/G]cacctataattccag | 285590 |
rs876926 | snp | C/T | 0.434253 | 0.168969 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172435676 | agcactttgggaggc[C/T]gaggcaggtagatcg | 285590 |
rs883989 | snp | C/T | 0.494651 | 0.0514399 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172415163 | GCAAATGTTTAACTG[C/T]GCCTTCTGTGAGGGA | 285590 |
rs889023 | snp | G/T | 0.406814 | 0.194704 | utr-variant-3-prime, intron-variant | SH3PXD2B | GRCh38.p7 | 5:172335096 | GGCCTTTGCTCACAT[G/T]TTCTGCTCGGAATCT | 285590 |
rs889024 | snp | A/G | 0.483995 | 0.0880135 | utr-variant-3-prime, intron-variant | SH3PXD2B | GRCh38.p7 | 5:172335773 | GGCAGTGGGTGGGTC[A/G]GGGTGGCCAGTCACT | 285590 |
rs892000 | snp | C/T | 0.482008 | 0.0931261 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172428923 | AAAGCCCTCTGTGAC[C/T]GCTCCCTGCCCACCA | 285590 |
rs892002 | snp | C/T | 0.499515 | 0.0155675 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172429221 | GGCAGGCCTTTGGTC[C/T]GTAGAAAGGGACCCT | 285590 |
rs919761 | snp | C/T | 0.293294 | 0.246223 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172440991 | TATAACCCCCTTCCA[C/T]GTAAGCAAGAGTGAG | 285590 |
rs919762 | snp | C/T | 0.0387552 | 0.1337 | upstream-variant-2KB | SH3PXD2B | GRCh38.p7 | 5:172455446 | TGTTTTTACAGAGGA[C/T]GGCCTCCAGACATTT | 285590 |
rs919763 | snp | C/T | 0.040671 | 0.13668 | upstream-variant-2KB | SH3PXD2B | GRCh38.p7 | 5:172455669 | AGTGCCTCCTAGCAC[C/T]GGCTGGGCACTGAGT | 285590 |
rs953136 | snp | A/T | | | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172436222 | CAGGCCAGCAGTGAA[A/T]CTGGCCTCCAAGAAG | 285590 |
rs953137 | snp | C/T | | | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172436149 | TGTGCCCCTATGGGC[C/T]TCTTACATAAGAGAC | 285590 |
rs953234 | snp | A/G | 0.448963 | 0.151372 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172434165 | GCATTTGGGGTATCC[A/G]TCCCCTCAAATATTT | 285590 |
rs1019934 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172443432 | ACCCCACTGCTAGTC[A/G]GCTTTCCCAGCCCCT | 285590 |
rs1035430 | snp | A/G | 0.455502 | 0.142369 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172328582 | TGTTCTCTATCTCTC[A/G]GATCCCACTCTCTCA | 285590 |
rs1035431 | snp | A/G | 0.474544 | 0.10991 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172328440 | aggccaaggcaggag[A/G]atcatttgaggccag | 285590 |
rs1108831 | snp | C/G | 0.0498117 | 0.149749 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172430183 | ataaaGAGAAACTGT[C/G]AGCAGCAGCATCATT | 285590 |
rs1139996 | snp | A/T | 0.498158 | 0.0302955 | utr-variant-3-prime, intron-variant | SH3PXD2B | GRCh38.p7 | 5:172333541 | TCCTTTTTTTTTTTT[A/T]AAATAAAAAAAGTGC | 285590 |
rs1368433 | snp | A/G | 0.349233 | 0.229462 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172447404 | TCATGGATATAGCAC[A/G]TTTTATCTTTGCATC | 285590 |
rs1433017 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172388131 | AGAGTCTGTCTATCC[G/T]TGTGCTAATACTGCA | 285590 |
rs1476134 | snp | C/T | 0.474723 | 0.109542 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172395222 | CATTATTTATTTTTA[C/T]AGCACTTCTTCTGTC | 285590 |
rs1476135 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172357626 | CTAGAGCCCTTGAGA[C/T]GGTGAATGATGACCA | 285590 |
rs1476136 | snp | A/G | 0.498253 | 0.0295011 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172357380 | CTGGAGTACAGTGGC[A/G]TGATCTCGGCTCACT | 285590 |
rs1541916 | snp | A/G | 0.494855 | 0.0504572 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172360116 | CCCGGCCGacagcac[A/G]tatttattatctaat | 285590 |
rs1541917 | snp | C/T | 0.354649 | 0.237831 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172359669 | GGCCCCATGCAGGCC[C/T]TTCTCATTGGGGAAT | 285590 |
rs1560682 | snp | A/C | 0.447809 | 0.152878 | upstream-variant-2KB | SH3PXD2B | GRCh38.p7 | 5:172456504 | CCACATCGTGCATTG[A/C]CTTATTAGGAGCCAA | 285590 |
rs1560683 | snp | A/G | 0.28578 | 0.247426 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172383708 | CTGCCCAAGCAGTGC[A/G]TGCTCTGCATGAGGC | 285590 |
rs1808387 | snp | A/T | | | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172329083 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 285590 |
rs1808650 | snp | A/G | 0.492037 | 0.0625946 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172431114 | TCAGGTGACCCACCC[A/G]CCTCGGCCTCCCAAA | 285590 |
rs1865002 | snp | C/T | 0.480539 | 0.0967035 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172385601 | TCTGCTAGAGGAGAC[C/T]TGGGTGGGTGTGGGG | 285590 |
rs1865003 | snp | A/C | 0.465578 | 0.126594 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172385617 | TGGGTGGGTGTGGGG[A/C]ATGGCCCCTGGAGGT | 285590 |
rs1982064 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172436407 | CCCGGGCTCCTTCAC[C/T]GGCCACAGCCCTATT | 285590 |
rs1982065 | snp | C/T | 0.491936 | 0.0629843 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172436548 | gggacttgcccaagg[C/T]cctgtagccagcagg | 285590 |
rs1982066 | snp | A/G | 0.493969 | 0.05458 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172436915 | CAGGACTATGTCCGA[A/G]GGTCCCTAGGAATCC | 285590 |
rs1982067 | snp | C/T | 0.375399 | 0.216275 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172436932 | GTCCCTAGGAATCCA[C/T]AGACCCCAGTTTCAG | 285590 |
rs1982068 | snp | A/G | 0.3752 | 0.216391 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172437160 | AGGGAAAGCAACAAG[A/G]GCAAGGGAGAGATGG | 285590 |
rs1982069 | snp | C/T | 0.3752 | 0.216391 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172437196 | GAGGAGAGGGCAGGG[C/T]GGTCGGATGGAGCTC | 285590 |
rs2005408 | snp | A/G | 0.378765 | 0.214288 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172434920 | tcccaagtagctggg[A/G]ttacaggcatgcacc | 285590 |
rs2012609 | snp | C/T | 0.195214 | 0.243923 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172429205 | AGGAGTGCTTCTCCT[C/T]GGCAGGCCTTTGGTC | 285590 |
rs2043285 | snp | A/G | 0.160938 | 0.233598 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172396271 | CCCAGCTACTCAGGA[A/G]GCTAAGGCAGGAGAA | 285590 |
rs2060225 | snp | C/T | 0.499575 | 0.0145705 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172410803 | CCTCTCATATACGAT[C/T]TCATGTGACCTTGAC | 285590 |
rs2060227 | snp | A/C | 0.152001 | 0.229992 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172413456 | GGCAGAAGAGAGGGC[A/C]AACAGTAGTAAGGGG | 285590 |
rs2060228 | snp | A/G | 0.360632 | 0.224189 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172413350 | TGGCAGCCTCCGTGC[A/G]GCACGTCCATCAGGA | 285590 |
rs2082409 | snp | G/T | 0.494609 | 0.0516363 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172401886 | taagctgaggatgta[G/T]gtcgcctcaggaccc | 285590 |
rs2082410 | snp | C/G | 0.49263 | 0.0602539 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172401969 | accttgaaaaaagaa[C/G]aggataacagcaatg | 285590 |
rs2099324 | snp | A/G | 0.125182 | 0.216612 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172380313 | CAATCCTTCCGCCTC[A/G]GCCTCCTAAAGTGCT | 285590 |
rs2116811 | snp | C/T | 0.118235 | 0.212457 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172393048 | TTGACTATTCTGGAT[C/T]CTTTATATTTCCACA | 285590 |
rs2163788 | snp | A/C | 0.469544 | 0.119585 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172425378 | TGGGCAGGACCCCGA[A/C]GTCTGCATGAGGGTG | 285590 |
rs2163789 | snp | A/G | 0.476918 | 0.104919 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172425419 | GGGCTGGCTACTTGG[A/G]TAAGGGGGCCTTGGA | 285590 |
rs2163790 | snp | C/T | 0.499891 | 0.00738737 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172425744 | ATTTGAA[C/T] | 285590 |
rs2163791 | snp | A/G | 0.472989 | 0.113031 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172398342 | taccatctatcaata[A/G]tcaggagcctgcagt | 285590 |
rs2247647 | snp | C/T | 0.498158 | 0.0302955 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172390040 | TTTtaacagatttac[C/T]gtggcataaattaca | 285590 |
rs2339423 | snp | C/T | 0.454423 | 0.143914 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172326735 | TATTTTGAATAGTTA[C/T]GTAAATACTTGTGTA | 285590 |
rs2339424 | snp | C/T | 0.454423 | 0.143914 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172327709 | ccctcctgtctcagc[C/T]tcctgagtatctgga | 285590 |
rs2339425 | snp | A/G | 0.454423 | 0.143914 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172327730 | agtatctggaactac[A/G]ggtgcataccactgc | 285590 |
rs2339426 | snp | C/T | 0.454302 | 0.144085 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172327745 | gggtgcataccactg[C/T]aactgggtttttttt | 285590 |
rs2339427 | snp | C/G | 0.436265 | 0.166749 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172327864 | ggttcaagcaattct[C/G]ctgcctcagccgccc | 285590 |
rs2339428 | snp | A/G | 0.491629 | 0.0641526 | utr-variant-3-prime, intron-variant | SH3PXD2B | GRCh38.p7 | 5:172335571 | TGCCGTAAGGATTAA[A/G]GGAGCGTGTGTGTTT | 285590 |
rs2436413 | snp | C/T | | | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172355548 | GATGGATTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 285590 |
rs2436414 | snp | C/T | 0.313082 | 0.241911 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172357098 | GGGGTCTCACTCTGT[C/T]ACTCAGGCTGGAGTG | 285590 |
rs2436415 | snp | C/T | 0.4983 | 0.0291038 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172356229 | AAACTGCTGTCATCA[C/T]GAGAGAATGGTGCCA | 285590 |
rs2468433 | snp | C/T | | | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172355543 | GCATGGATGGATTTT[C/T]TTTTCTTTTTTTTTT | 285590 |
rs2468434 | snp | A/G | 0.484771 | 0.0859212 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172368423 | TCGTAGGCCTGTGAT[A/G]TGTTTTGGTGCAAGG | 285590 |
rs2468435 | snp | C/T | 0.475525 | 0.107882 | intron-variant | SH3PXD2B | GRCh38.p7 | 5:172372332 | AAGTGTGTAGCACTG[C/T]CCCTCTCTCTCTTGG | 285590 |
rs2569208 | snp | C/T | 0.496416 | 0.0421803 | | | GRCh38.p7 | 5:172373379 | AGCTCTCAGCTACCA[C/T]ATTGCTCTGTATAAA | 285590 |
rs2569209 | snp | A/G | 0.493293 | 0.0575177 | | | GRCh38.p7 | 5:172374371 | TTACCGTCGTCACCC[A/G]TGTCAGAGTTTATAA | 285590 |
rs2569210 | snp | C/T | 0.340108 | 0.233197 | | | GRCh38.p7 | 5:172440253 | TGTCTTCAAGGAGCA[C/T]GCGGTCGAGATGGCA | 285590 |
rs2569211 | snp | C/T | 0.34303 | 0.232046 | | | GRCh38.p7 | 5:172440305 | TCCTACACAATCACC[C/T]GCCTGGGTTTCTGCC | 285590 |
rs2569212 | snp | A/G | 0.476918 | 0.104919 | | | GRCh38.p7 | 5:172454002 | TGGGGGGACACGGAG[A/G]AGACAGAAAGGGGTA | 285590 |
rs2569213 | snp | C/G | 0.324855 | 0.23853 | | | GRCh38.p7 | 5:172430204 | CAGCATCATTGTGAG[C/G]AGAAGGTCACAAAGG | 285590 |
rs2569214 | snp | C/T | 0.449473 | 0.150701 | | | GRCh38.p7 | 5:172431216 | CAGCTGACTGGCTCA[C/T]GGACACCATCACGTG | 285590 |
rs2569215 | snp | A/G | 0.492137 | 0.0622048 | | | GRCh38.p7 | 5:172431224 | TGGCTCATGGACACC[A/G]TCACGTGATCCAAGC | 285590 |
rs2569216 | snp | C/G | 0.487871 | 0.076925 | | | GRCh38.p7 | 5:172432677 | atcccagcattttgg[C/G]aggccgaggcagatg | 285590 |
rs2569217 | snp | A/G | 0.492582 | 0.0604491 | | | GRCh38.p7 | 5:172433073 | gtaagattataacac[A/G]gtatttttacaaaac | 285590 |
rs2569218 | snp | C/T | 0.4582 | 0.138394 | | | GRCh38.p7 | 5:172434725 | AAGGGCTGGGGCTGC[C/T]GCACTGGTCCCATGA | 285590 |
rs2569219 | snp | A/G | 0.462034 | 0.132445 | | | GRCh38.p7 | 5:172437493 | TGGGAAGTGGGTGAC[A/G]TGAGATCCAATCCCA | 285590 |
rs2569220 | snp | C/T | 0.322959 | 0.239117 | | | GRCh38.p7 | 5:172438089 | CTGTGCAGTCTGCCC[C/T]TCCTCTGCTCCAGCC | 285590 |
rs2569221 | snp | C/T | 0.493748 | 0.0555599 | | | GRCh38.p7 | 5:172383485 | GCTCGTTGAAGGATC[C/T]GAAACTCAGACATGG | 285590 |
rs2569222 | snp | C/T | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 5:172409377 | acaagagcaaaactc[C/T]gtctcaaaacaaaaa | 285590 |
rs2569223 | snp | A/G | 0.477004 | 0.104734 | | | GRCh38.p7 | 5:172379666 | GCACTACCATGAGCC[A/G]CCACTTCCTGAGCAG | 285590 |
rs2569224 | snp | A/G | 0.462144 | 0.132269 | | | GRCh38.p7 | 5:172379689 | CTGAGCAGCTGGCAA[A/G]GTCTTAGAATTTTTC | 285590 |
rs2569225 | snp | A/G | 0.492287 | 0.0616198 | | | GRCh38.p7 | 5:172380827 | AAGCTGTGTTTACTC[A/G]CTCCGTGCTCGTCAC | 285590 |
rs2569226 | snp | C/T | 0.495671 | 0.0463237 | | | GRCh38.p7 | 5:172381762 | GCCTCACGGGCTCAG[C/T]CTGCTCAGTTCCGAC | 285590 |
rs2569227 | snp | C/G | 0.498253 | 0.0295011 | | | GRCh38.p7 | 5:172360891 | TAGGTTAGATTCCAA[C/G]AAGTGAAACAGCTGG | 285590 |
rs2569228 | snp | A/G | 0.339429 | 0.233457 | | | GRCh38.p7 | 5:172360818 | TGGAGACGGAGACTC[A/G]CTCTGTTGCCCCGGC | 285590 |
rs2569229 | snp | C/T | 0.495213 | 0.048687 | | | GRCh38.p7 | 5:172360721 | tctcagcctcccaag[C/T]agctgggactacagg | 285590 |
rs2569230 | snp | A/T | 0.495213 | 0.048687 | | | GRCh38.p7 | 5:172360701 | gggactacaggcaca[A/T]gccaccatgcctggt | 285590 |
rs2569231 | snp | A/G | 0.498459 | 0.0277128 | | | GRCh38.p7 | 5:172360401 | ggtttgaatcctggc[A/G]ctgctgctttctatc | 285590 |
rs2569232 | snp | C/T | 0.383555 | 0.211336 | | | GRCh38.p7 | 5:172358888 | ATCATTCTGCACTCT[C/T]GCTTCCCCAGGTTGG | 285590 |
rs2569233 | snp | C/T | 0.498277 | 0.0293024 | | | GRCh38.p7 | 5:172358378 | TTTAAAAACCTCTGC[C/T]TTCTCTGTGGGTTTA | 285590 |
rs2569237 | snp | A/C | 0.467337 | 0.123551 | | | GRCh38.p7 | 5:172369896 | CTCACAGTCTGGTAG[A/C]AAAGAGACCTGTATA | 285590 |
rs2569238 | snp | A/C | 0.49928 | 0.018956 | | | GRCh38.p7 | 5:172368122 | gggaacagcaaatgc[A/C]aaattccctgcagta | 285590 |