| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs584134455 | snp | C/T | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142645342 | GATTTAAACCTAGAA[C/T]CCTGTGGAGCCCACT | 74781 |
| rs584329521 | snp | C/T | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142660503 | GGTTTCTCTGTGTAG[C/T]CCTGGCTGTCCTGGA | 74781 |
| rs584330224 | snp | A/G | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142643222 | CCACCAGTTTTGTCA[A/G]TAAGATAGAACATTG | 74781 |
| rs584455180 | snp | A/G | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142652931 | CTAACCAGTACCCCC[A/G]GAGCTCCTTGGGACT | 74781 |
| rs584679646 | snp | A/G | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142658642 | TCCTCTGCCTAATAC[A/G]CACCTTGGCGCGCAC | 74781 |
| rs584688329 | snp | C/G | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142635415 | GGACCTCCCCTAAAG[C/G]TCATTTTGTGATTTC | 74781 |
| rs584712702 | snp | G/T | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142651405 | GGTTTGTTTGGTTTT[G/T]TTTTGTTTTGTTTTG | 74781 |
| rs584802944 | snp | A/G | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142643096 | AGCACCAGGCCGTCC[A/G]CAACACTTGCCCCTT | 74781 |
| rs584944864 | snp | C/T | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142643800 | CAAGTGAATAAATAA[C/T]ATTAACTGTCACATT | 74781 |
| rs584974407 | snp | A/G | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142634654 | AGGATAGCCAGGGCT[A/G]CACAGAGAAACCCTG | 74781 |
| rs584998377 | snp | C/G | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142645399 | AGACATGTTAGAGCA[C/G]TATATCCTTATACCA | 74781 |
| rs585052397 | snp | C/G | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142663190 | TTTTGTTATTGTTTG[C/G]GGTTTTTGTTTGTTT | 74781 |
| rs585199204 | snp | A/G | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142665798 | TGAGGCTTGGGGTCT[A/G]TAGTAAGTGTCTTCC | 74781 |
| rs585255223 | snp | A/G | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142648452 | CCGGTGTCCTGGGAA[A/G]CCAGTTCTTCACTGA | 74781 |
| rs585331773 | snp | A/G | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142666322 | GCCTCCCGTGAAGCC[A/G]TGGGCCAGGGCGCCT | 74781 |
| rs585474070 | snp | A/G | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142645920 | TTTTAGTGGATTCTT[A/G]CCCAACACGTTGGTT | 74781 |
| rs585541069 | snp | C/T | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142644283 | AGGGAACTGGGGCGA[C/T]GACTCTTCATAACTT | 74781 |
| rs585554108 | snp | A/G | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142646075 | TGAACCAATCCCCTA[A/G]TGAATAAAGGAGCCA | 74781 |
| rs585688704 | snp | C/T | | | intron-variant, upstream-variant-2KB | Wipi2, LOC105242553 | GRCm38.p3 | 5:142630681 | GCTCAGTTGGACCTT[C/T]AGACGAGCTCAAGAA | 74781 |
| rs585789910 | snp | A/G | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142662014 | CTTTGAGAAAAGACA[A/G]ATCCCAGACACTGAT | 74781 |
| rs585795846 | snp | C/T | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142662582 | TGCCGGGCGTGGTGG[C/T]GCATGCCTTTAATCC | 74781 |
| rs585806609 | snp | A/G | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142641101 | TCCCTCCCTCCCTCC[A/G]TTCTCCCACCCATCT | 74781 |
| rs586020932 | snp | C/T | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142654211 | GTGTGTGTGTGCGTG[C/T]GTTTCATATACAGAC | 74781 |
| rs586047289 | snp | A/T | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142644028 | TAATACCTGTACTTT[A/T]TAATTTTTCGTATCA | 74781 |
| rs586143339 | snp | C/T | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142639595 | TCTGAGTTCGAAGGC[C/T]AGCCTGGTCTACAAA | 74781 |
| rs586239443 | snp | C/T | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142642509 | ACCCAATGAGGAGGA[C/T]ACTGAGGCTATCATC | 74781 |
| rs586345085 | snp | A/T | | | upstream-variant-2KB, downstream-variant-500B | Wipi2, LOC105242553 | GRCm38.p3 | 5:142628513 | TTGCATGAAATTCTT[A/T]AAGAATTCATTAAAA | 74781 |
| rs586360698 | snp | C/G | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142646309 | AGGTATGGCGACAAA[C/G]CGTGGGTTTTCTAGA | 74781 |
| rs586460082 | snp | A/G | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142644687 | TGTCCTTGAGCCAGT[A/G]ATCAGCAAACCCTTT | 74781 |
| rs586468001 | snp | C/T | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142654201 | GTGTGTGTGTGTGTG[C/T]GTGTGCGTGTGTTTC | 74781 |
| rs586578661 | snp | C/T | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142647798 | TGGTGAACTTTGAGT[C/T]TCCTCTCCTCTCCTC | 74781 |
| rs586583035 | snp | C/T | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142646810 | CATATTACTTTATAA[C/T]CCTCATTTCTACAAC | 74781 |
| rs586761072 | snp | C/T | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142634861 | CTGTCCTGGAACTCA[C/T]TTTGTAGACCAGGCT | 74781 |
| rs586838447 | snp | A/G | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142631970 | CGCCACCACTGCCCG[A/G]CCAGATTTTTTTTTA | 74781 |
| rs586858903 | snp | A/T | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142645266 | CCTTTATACCATCTT[A/T]ACACAATTGATTCAC | 74781 |
| rs587027357 | snp | A/G | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142663159 | TAAGTGGCAAAGACA[A/G]GCTTGTCTTTCCTTC | 74781 |
| rs587136624 | snp | G/T | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142656221 | TAAGTGCTCTTGCTG[G/T]ATAAATATAGGGACT | 74781 |
| rs587185998 | snp | C/G | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142643115 | CACTTGCCCCTTTCT[C/G]TTCTAATAAAAACAA | 74781 |
| rs587190856 | snp | G/T | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142663194 | GTTATTGTTTGGGGT[G/T]TTTGTTTGTTTGTTT | 74781 |
| rs587288576 | snp | A/G | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142644867 | TCAAGATTCCCATGG[A/G]GCCCATTTTAGCAGA | 74781 |
| rs587389173 | snp | A/C | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142643072 | GTTAGGGGATTGGTT[A/C]ACAAGAACAGCACCA | 74781 |
| rs587481535 | snp | A/G | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142633844 | GGTTTTTTTTTTTGA[A/G]ACAGGGTTTCTCTGT | 74781 |
| rs864265382 | snp | A/G | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142664802 | CGTGGAGTGCCGGCA[A/G]GCTTGTCTGTAAGAC | 74781 |
| rs864291103 | snp | A/C/G | | | intron-variant | Wipi2 | GRCm38.p3 | 5:142662682 | AGGACAGCCAGGGCT[A/C/G]TACAGAGAAACCCTG | 74781 |