SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs750162 | snp | G/T | 0.484841 | 0.0857308 | intron-variant | DMXL2 | GRCh38.p7 | 15:51614956 | agacagcatcatttt[G/T]ttcccctggataatg | 23312 |
rs750163 | snp | C/T | 0.47934 | 0.0995154 | intron-variant | DMXL2 | GRCh38.p7 | 15:51614790 | cacgtggcttttttt[C/T]ccactcagaataaaa | 23312 |
rs882385 | snp | A/G | 0.489083 | 0.0730708 | intron-variant | DMXL2 | GRCh38.p7 | 15:51590172 | ACCACATCATAGCTT[A/G]CTGGCTAGCCTATGG | 23312 |
rs882386 | snp | C/T | 0.449345 | 0.150869 | intron-variant | DMXL2 | GRCh38.p7 | 15:51590076 | TGTTGATCACGTGGT[C/T]TGCCAGGGCTGCTCT | 23312 |
rs930919 | snp | A/G | 0.441295 | 0.160954 | intron-variant | DMXL2 | GRCh38.p7 | 15:51460154 | GTTATTTCTTTTTCC[A/G]TGCCTGATTTTATTA | 23312 |
rs930920 | snp | G/T | 0.450105 | 0.149859 | intron-variant | DMXL2 | GRCh38.p7 | 15:51457529 | ACATAAGAAGATTTT[G/T]AGTTGGAATTTGTGT | 23312 |
rs936310 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | DMXL2 | GRCh38.p7 | 15:51588486 | GAACAAATTGAGAAA[C/T]AGTATTGTGGCTGGG | 23312 |
rs956171 | snp | A/G | 0.224709 | 0.248717 | intron-variant | DMXL2 | GRCh38.p7 | 15:51544941 | TATATGCATTATTTT[A/G]AATTGTCAGAAATTT | 23312 |
rs977137 | snp | C/G | 0.161924 | 0.233971 | intron-variant | DMXL2 | GRCh38.p7 | 15:51460659 | TAAATTTGGCAAATT[C/G]AGAAAATTGACCAAT | 23312 |
rs1031664 | snp | G/T | 0.486133 | 0.082104 | intron-variant | DMXL2 | GRCh38.p7 | 15:51462700 | AGGTAATTAGTGAGG[G/T]AATGAGCAGTTTGAA | 23312 |
rs1077361 | snp | A/T | 0.489083 | 0.0730708 | intron-variant | DMXL2 | GRCh38.p7 | 15:51588722 | TTACAGTTTAATAGT[A/T]TAATCACAATTTAAT | 23312 |
rs1080394 | snp | A/G | 0.446249 | 0.154875 | intron-variant | DMXL2 | GRCh38.p7 | 15:51465424 | AAGTCACAGATTGGA[A/G]CCTAAAATAAACAAG | 23312 |
rs1551657 | snp | G/T | 0.224709 | 0.248717 | intron-variant | DMXL2 | GRCh38.p7 | 15:51469087 | TCACCAGTTGCATCT[G/T]AAATGTTTTTATATA | 23312 |
rs1902591 | snp | C/T | | | | | GRCh38.p7 | 15:51560723 | TAGTTTTCCACAGTT[C/T]TGAACTTAACAGAGT | 23312 |
rs1902592 | snp | C/T | 0.489083 | 0.0730708 | intron-variant | DMXL2 | GRCh38.p7 | 15:51589783 | TTCTGGAAAATAATT[C/T]GATATTATGAATTAA | 23312 |
rs1902593 | snp | C/T | 0.489142 | 0.0728777 | | | GRCh38.p7 | 15:51589883 | AAACATCCAGACATG[C/T]AAACAAAGATCACAA | 23312 |
rs1902594 | snp | C/T | 0.494936 | 0.050064 | intron-variant | DMXL2 | GRCh38.p7 | 15:51613301 | ATTTATGTTCAGAGA[C/T]TGCAGTAAAGACAGG | 23312 |
rs1902595 | snp | C/T | 0.225005 | 0.248747 | intron-variant | DMXL2 | GRCh38.p7 | 15:51613518 | TGCACAATGTCTAGG[C/T]GCCAAAATATTTTTT | 23312 |
rs1902596 | snp | A/G | 0.178465 | 0.239547 | intron-variant | DMXL2 | GRCh38.p7 | 15:51618678 | TGAAGAAGTCCTGTG[A/G]TTAAAAAGTAACTTT | 23312 |
rs1902597 | snp | C/T | 0.00835141 | 0.0640778 | upstream-variant-2KB | DMXL2 | GRCh38.p7 | 15:51622937 | GAGGTAGAGCCCTCC[C/T]CCCGCGGCAAAGCTC | 23312 |
rs1902598 | snp | C/T | 0.0452528 | 0.143452 | | | GRCh38.p7 | 15:51622992 | TCACCCGCGTTTGCG[C/T]GTGCGCGCGCCGTGG | 23312 |
rs1902599 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | DMXL2 | GRCh38.p7 | 15:51623115 | AGCCGCTGCGGACTG[A/G]GGCGGAGGTGGGGGC | 23312 |
rs1914016 | snp | C/T | 0.0324675 | 0.123206 | missense, nc-transcript-variant | DMXL2 | GRCh38.p7 | 15:51488548 | GTCAAGGCAACTTAC[C/T]TAAACAGACCCCACA | 23312 |
rs1914017 | snp | C/T | 0 | 0 | splice-acceptor-variant | DMXL2 | GRCh38.p7 | 15:51488646 | AGAAGCTTTGGCAAC[C/T]TAAATGATAAATAAA | 23312 |
rs1914019 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | DMXL2 | GRCh38.p7 | 15:51528566 | ggggtcaattcagca[A/C]gagaatataacaatt | 23312 |
rs2061425 | snp | A/G | 0.230017 | 0.2492 | intron-variant | DMXL2 | GRCh38.p7 | 15:51455949 | ATTTAAACTGAGTAG[A/G]CAGTTTGTTGGAGTC | 23312 |
rs2090356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DMXL2 | GRCh38.p7 | 15:51524965 | accccaggctgtaca[A/G]ctcacggctccaaag | 23312 |
rs2124875 | snp | A/T | 0.473909 | 0.111197 | intron-variant | DMXL2 | GRCh38.p7 | 15:51541172 | TGTTGTTTTGCTTAT[A/T]TTATCCTTTCTTATC | 23312 |
rs2124876 | snp | C/T | 0.489665 | 0.0711382 | intron-variant | DMXL2 | GRCh38.p7 | 15:51613965 | AGCTGATTGTTAACA[C/T]GTGTTGTGGACTATA | 23312 |
rs2124877 | snp | A/G | 0.484841 | 0.0857308 | intron-variant | DMXL2 | GRCh38.p7 | 15:51614078 | ATAAGGTTAAATGAG[A/G]TCTTAAGGGTGGGGC | 23312 |
rs2124878 | snp | C/T | 0.484841 | 0.0857308 | intron-variant | DMXL2 | GRCh38.p7 | 15:51614140 | AAGACACCGCAAGTG[C/T]ATGTACACAAAGGAA | 23312 |
rs2124879 | snp | C/T | 0.489376 | 0.0721049 | upstream-variant-2KB, nc-transcript-variant | DMXL2, LOC105370816 | GRCh38.p7 | 15:51624636 | TTGATAGCTGTATCT[C/T]AAGGTTGCAAATGAC | 23312 |
rs2271674 | snp | G/T | 0.138207 | 0.223612 | intron-variant | DMXL2 | GRCh38.p7 | 15:51457565 | TAGGACAATCTTTAT[G/T]TTAAAAACTAAGTAG | 23312 |
rs2271675 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | DMXL2 | GRCh38.p7 | 15:51463255 | TAGTTCACGGTAGTT[C/T]AGTGAACTTTGACTA | 23312 |
rs2271676 | snp | A/G | 0.16911 | 0.236552 | intron-variant | DMXL2 | GRCh38.p7 | 15:51474282 | CTTGAAACATTAAAA[A/G]AAATTTTAACATTCA | 23312 |
rs2271677 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | DMXL2 | GRCh38.p7 | 15:51480242 | TAAAGGGAATATGTT[C/T]GCTCACTCATTCTAC | 23312 |
rs2278988 | snp | G/T | 0.489376 | 0.0721049 | upstream-variant-2KB | DMXL2 | GRCh38.p7 | 15:51623037 | TCACGGGACGGCGGG[G/T]CGGCGTGGCGCGCGC | 23312 |
rs2278989 | snp | A/G | 0.499878 | 0.00780463 | synonymous-codon, nc-transcript-variant | DMXL2 | GRCh38.p7 | 15:51622519 | TCAGGTCCTCACCGG[A/G]GCTGTCAACCCTGGA | 23312 |
rs2278990 | snp | C/T | 0.5 | 0.000186997 | synonymous-codon, nc-transcript-variant | DMXL2 | GRCh38.p7 | 15:51622465 | CGTCGGGGATGTCCC[C/T]TTCACGGTGAGCGGC | 23312 |
rs2305708 | snp | C/T | 0.48491 | 0.0855403 | intron-variant | DMXL2 | GRCh38.p7 | 15:51617763 | GTTTAAGTGATTTCA[C/T]CAACACCATACAAGT | 23312 |
rs2414104 | snp | A/G | 0.439085 | 0.163545 | intron-variant | DMXL2 | GRCh38.p7 | 15:51524474 | acagtacccagtttt[A/G]acttcattatcactg | 23312 |
rs2414105 | snp | A/G | 0.499997 | 0.00129366 | synonymous-codon, nc-transcript-variant | DMXL2 | GRCh38.p7 | 15:51576176 | ATCACAGCCTGATCC[A/G]TATGCCTAAAAAAAA | 23312 |
rs2414106 | snp | C/T | 0.488424 | 0.0751925 | intron-variant | DMXL2 | GRCh38.p7 | 15:51576544 | AAAAATACTAAGCCA[C/T]TGAAGACTGTAACTG | 23312 |
rs2414107 | snp | A/T | 0.488905 | 0.0736498 | intron-variant | DMXL2 | GRCh38.p7 | 15:51585359 | gttgaattttgtcaa[A/T]ggctttttctgcatc | 23312 |
rs2414108 | snp | A/G | 0.438526 | 0.164189 | intron-variant | DMXL2 | GRCh38.p7 | 15:51608275 | aaaggaatataaatc[A/G]ttataccatgaagac | 23312 |
rs2414109 | snp | C/G | 0.489142 | 0.0728777 | intron-variant | DMXL2 | GRCh38.p7 | 15:51608818 | caacactaacagatt[C/G]ataccaaggaaattc | 23312 |
rs2414110 | snp | C/T | 0.482683 | 0.0914256 | intron-variant | DMXL2 | GRCh38.p7 | 15:51609105 | GAAATAAGTTAAGAA[C/T]GCATCCTGTAATTTC | 23312 |
rs2414111 | snp | C/T | 0.489083 | 0.0730708 | intron-variant | DMXL2 | GRCh38.p7 | 15:51609160 | aacagaatatggagt[C/T]ttaggactagaggga | 23312 |
rs2414112 | snp | C/T | 0.229136 | 0.249128 | intron-variant | DMXL2 | GRCh38.p7 | 15:51610827 | ATAAACTTAAAAAGA[C/T]TAGAAGTACATACCG | 23312 |
rs2414113 | snp | C/T | 0.489142 | 0.0728777 | intron-variant | DMXL2 | GRCh38.p7 | 15:51611699 | AAAGTATTAGTATCC[C/T]CATCTATGAAATtga | 23312 |
rs2414114 | snp | G/T | 0.489376 | 0.0721049 | intron-variant | DMXL2 | GRCh38.p7 | 15:51613584 | CTGGGAACTGGAAAC[G/T]TTCAGTTTTACTTTC | 23312 |
rs2899475 | snp | C/T | 0.489083 | 0.0730708 | intron-variant | DMXL2 | GRCh38.p7 | 15:51590854 | TATATTTTGCTAGGA[C/T]AGGAGGAGAGAGAGA | 23312 |
rs2899476 | snp | C/T | 0.489142 | 0.0728777 | intron-variant | DMXL2 | GRCh38.p7 | 15:51611677 | CATTAAATCATTTAA[C/T]TTCTCAAAAGTATTA | 23312 |
rs3078066 | in-del | -/AAA/AAAAA/AT/T | | | intron-variant | DMXL2 | GRCh38.p7 | 15:51576203 | aaaaaaaaaaaaaaa[-/AAA/AAAAA/AT/T]GTTTTACAATACATA | 23312 |
rs3078071 | in-del | -/TAAGT | 0.488726 | 0.0742286 | intron-variant | DMXL2 | GRCh38.p7 | 15:51609094 | CTTCAATAAGTGAAA[-/TAAGT]TAAGAATGCATCCTG | 23312 |
rs3206942 | snp | A/G | 0 | 0 | intron-variant | DMXL2 | GRCh38.p7 | 15:51567313 | tggctcacacctgta[A/G]tcccaacactttggg | 23312 |
rs3736484 | snp | A/T | 0.0491569 | 0.148869 | intron-variant | DMXL2 | GRCh38.p7 | 15:51456386 | TTTAAAAGAAAATTT[A/T]AAAAATTTTATTTTG | 23312 |
rs3736485 | snp | A/G | 0.498912 | 0.0232954 | intron-variant | DMXL2 | GRCh38.p7 | 15:51456413 | TTTGTGTATGCAGAA[A/G]AGATGAGGAAGGATA | 23312 |
rs3751584 | snp | C/T | 0.00726149 | 0.0598165 | synonymous-codon, nc-transcript-variant | DMXL2 | GRCh38.p7 | 15:51481160 | TTGGGGTGAAGATCA[C/T]GACAGTGCCTTAGAT | 23312 |
rs3751585 | snp | C/T | 0.201727 | 0.245295 | utr-variant-3-prime, nc-transcript-variant | DMXL2 | GRCh38.p7 | 15:51448859 | AGAATTTGAATATGA[C/T]CCAAGCTGAGTATTA | 23312 |
rs3830518 | in-del | -/GCA | | | intron-variant | DMXL2 | GRCh38.p7 | 15:51458919 | gcagcagcagcagca[-/GCA]AGAAAAAAGGGTAAG | 23312 |
rs4143721 | snp | A/G | 0.488545 | 0.074807 | intron-variant | DMXL2 | GRCh38.p7 | 15:51574584 | AAAAGTGTTGTGAAT[A/G]ATTCCATTCAACATG | 23312 |
rs4143722 | snp | C/G | 0.473909 | 0.111197 | intron-variant | DMXL2 | GRCh38.p7 | 15:51574994 | GAAATCTGACACTCC[C/G]CATGTTTTCTAAACT | 23312 |
rs4143723 | snp | A/G | 0.488606 | 0.0746142 | intron-variant | DMXL2 | GRCh38.p7 | 15:51574975 | CAACAAAAAATTAAA[A/G]AGAGAAATCTGACAC | 23312 |
rs4143724 | snp | A/T | 0.488545 | 0.074807 | intron-variant, upstream-variant-2KB | DMXL2 | GRCh38.p7 | 15:51578216 | TTTGCCCAAGATTAC[A/T]GTTACTAAATGCAAA | 23312 |
rs4144941 | snp | C/T | 0.489259 | 0.0724914 | intron-variant | DMXL2 | GRCh38.p7 | 15:51504609 | AGAGCACCAGAATAT[C/T]CAATAAATAATAATC | 23312 |
rs4359386 | snp | C/T | 0.487809 | 0.0771174 | intron-variant | DMXL2 | GRCh38.p7 | 15:51533926 | AAGCAAAAACAAATA[C/T]ATTAAATAACATAAT | 23312 |
rs4436729 | snp | A/G | 0.427119 | 0.176434 | intron-variant | DMXL2 | GRCh38.p7 | 15:51591320 | ggtcctacgcccaca[A/G]agcctcgctcattgc | 23312 |
rs4438255 | snp | A/G | 0.489083 | 0.0730708 | intron-variant | DMXL2 | GRCh38.p7 | 15:51591154 | cctcacccaggaagc[A/G]caaggggtcagggaa | 23312 |
rs4462536 | snp | A/G | 0.487746 | 0.0773096 | intron-variant | DMXL2 | GRCh38.p7 | 15:51534082 | caaggtttagcagag[A/G]gcagggagggggaaa | 23312 |
rs4462537 | snp | A/G | 0.474723 | 0.109542 | intron-variant | DMXL2 | GRCh38.p7 | 15:51534321 | GCACAGGGGGAGCAG[A/G]TTTGGCCTGAGGTAG | 23312 |
rs4465557 | snp | C/G | 0.227074 | 0.248947 | intron-variant | DMXL2 | GRCh38.p7 | 15:51591440 | agcggtgggaagctc[C/G]aactgggtggagccc | 23312 |
rs4545756 | snp | A/G | 0.489083 | 0.0730708 | intron-variant | DMXL2 | GRCh38.p7 | 15:51585593 | aaattctaagatata[A/G]tatgctggatcagtg | 23312 |
rs4774590 | snp | A/G | 0.451234 | 0.14834 | intron-variant | DMXL2 | GRCh38.p7 | 15:51453080 | taatggactctgggg[A/G]cttgggaggggtggg | 23312 |
rs4774591 | snp | C/T | 0.479095 | 0.100076 | intron-variant | DMXL2 | GRCh38.p7 | 15:51477988 | TAGAAAATTTCATAT[C/T]ATAAGTTATTATGGA | 23312 |
rs4774592 | snp | C/T | 0.493748 | 0.0555599 | intron-variant | DMXL2 | GRCh38.p7 | 15:51486682 | CTCTTAATTTCCAAA[C/T]ATATTTCTGCATAAT | 23312 |
rs4774593 | snp | A/G | 0.474453 | 0.110094 | intron-variant | DMXL2 | GRCh38.p7 | 15:51529648 | aaagcccaggaccca[A/G]tggttttgctgctga | 23312 |
rs4774594 | snp | C/T | 0.225597 | 0.248806 | intron-variant | DMXL2 | GRCh38.p7 | 15:51559802 | ttaaaagtcagacca[C/T]atcagcactggctag | 23312 |
rs4774595 | snp | C/T | 0.489259 | 0.0724914 | intron-variant | DMXL2 | GRCh38.p7 | 15:51600964 | tctccagagagttta[C/T]agacactctcaagaa | 23312 |
rs4774596 | snp | A/C | 0.484841 | 0.0857308 | intron-variant | DMXL2 | GRCh38.p7 | 15:51618778 | TCTTTCCAAACCTTA[A/C]TCTTCCATAAAACCT | 23312 |
rs4775943 | snp | A/G | 0.47885 | 0.100637 | intron-variant | DMXL2 | GRCh38.p7 | 15:51477908 | GTATTTTTTATTTCA[A/G]TGGATAATTAGTTAA | 23312 |
rs4775944 | snp | C/T | 0.494358 | 0.0528145 | intron-variant | DMXL2 | GRCh38.p7 | 15:51483413 | CAGAGCCTAGGACCA[C/T]GACTGGCTATGACTT | 23312 |
rs4775945 | snp | A/C | 0.435407 | 0.167703 | intron-variant | DMXL2 | GRCh38.p7 | 15:51483712 | tgcgcctgcaatcaa[A/C]gcctgagaaatagtc | 23312 |
rs4775946 | snp | A/G | 0.494358 | 0.0528145 | intron-variant | DMXL2 | GRCh38.p7 | 15:51483733 | agaaatagtccttcg[A/G]gccgcccctggcagc | 23312 |
rs4775948 | snp | A/G | 0.486332 | 0.08153 | intron-variant | DMXL2 | GRCh38.p7 | 15:51521470 | AGTAGTAGTGGTAGT[A/G]GTAGTAGTAGTAGTA | 23312 |
rs4775950 | snp | C/T | 0.436976 | 0.165952 | intron-variant | DMXL2 | GRCh38.p7 | 15:51556677 | CTTGGGAAGCTGAAA[C/T]GGGAGAAATACTTGA | 23312 |
rs4775951 | snp | C/T | 0.490508 | 0.0682328 | intron-variant | DMXL2 | GRCh38.p7 | 15:51570903 | aataaccagctagca[C/T]cataatgacaggatt | 23312 |
rs4775952 | snp | C/T | 0.494815 | 0.0506538 | intron-variant, upstream-variant-2KB | DMXL2 | GRCh38.p7 | 15:51576859 | AAAATAGAAAATGAA[C/T]GAATTTATATAGAAT | 23312 |
rs4775953 | snp | G/T | 0.489142 | 0.0728777 | intron-variant | DMXL2 | GRCh38.p7 | 15:51580976 | AGGTCTCTGAACTCC[G/T]AAAAATTGTATTTAA | 23312 |
rs4775954 | snp | G/T | 0.200801 | 0.245111 | intron-variant | DMXL2 | GRCh38.p7 | 15:51581210 | GATTCTCATAGGAAC[G/T]CAAGCCCTATTGTAA | 23312 |
rs4775955 | snp | C/T | 0.489142 | 0.0728777 | intron-variant | DMXL2 | GRCh38.p7 | 15:51581252 | TAGGGATGTAGGCTG[C/T]ATGCTCTTTATGAGA | 23312 |
rs4775956 | snp | C/G | 0.489083 | 0.0730708 | intron-variant | DMXL2 | GRCh38.p7 | 15:51590441 | GAGTCCCTGATAACT[C/G]AGGCTCAGCTGTACT | 23312 |
rs4775958 | snp | C/G | 0.489083 | 0.0730708 | intron-variant | DMXL2 | GRCh38.p7 | 15:51599365 | gtatcactgcttcta[C/G]gcctctcagctgaca | 23312 |
rs4775959 | snp | C/T | 0.489201 | 0.0726845 | intron-variant | DMXL2 | GRCh38.p7 | 15:51599439 | agacagacacacaca[C/T]atctattttcaactg | 23312 |
rs4775960 | snp | C/G | 0.489142 | 0.0728777 | intron-variant | DMXL2 | GRCh38.p7 | 15:51599501 | ccaataCAAacatcc[C/G]tatcatatctacata | 23312 |
rs4775961 | snp | A/G | 0.489259 | 0.0724914 | intron-variant | DMXL2 | GRCh38.p7 | 15:51600762 | agggtatctgccagt[A/G]taagtttcctgtgag | 23312 |
rs4775962 | snp | C/T | 0.155987 | 0.23165 | intron-variant | DMXL2 | GRCh38.p7 | 15:51610534 | AGAACTTTGGGAGGC[C/T]GAGGCGGGCAGATCA | 23312 |
rs4775963 | snp | C/T | 0.484491 | 0.0866827 | intron-variant | DMXL2 | GRCh38.p7 | 15:51612615 | gaatagggtgtgggt[C/T]acagagatcatatgc | 23312 |
rs4775965 | snp | A/G | 0.484491 | 0.0866827 | intron-variant | DMXL2 | GRCh38.p7 | 15:51616054 | CAACAATTATTTAGT[A/G]TGAATTAAATTAAAT | 23312 |
rs4775966 | snp | A/G | 0.489665 | 0.0711382 | intron-variant | DMXL2 | GRCh38.p7 | 15:51621591 | TCCAAGGCTTGGTTT[A/G]AACATTTCCACTCTC | 23312 |