| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs246301601 | snp | A/G | | | intron-variant, utr-variant-5-prime | Arhgef37 | Mm_Celera | 18:61512100 | TCCCTCTGAACACTC[A/G]GAGTCTGAACAGGTC | 328967 |
| rs246454291 | in-del | -/TTT | | | intron-variant, upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61513681 | GAAGTTTTTGTTTTG[-/TTT]TTTTGTTTTTTTAAT | 328967 |
| rs246550456 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61509213 | AGCCCTTTCCTCCAC[A/G]TGTGCCCTTGGTGGC | 328967 |
| rs246626366 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61501943 | GAGGCAGCTGGGTGG[A/G]AAGATGCTGTCAGCA | 328967 |
| rs246638365 | snp | A/T | | | intron-variant, downstream-variant-500B | Arhgef37 | Mm_Celera | 18:61505127 | TATATCTAGGTCACA[A/T]AGAAGTTCCTCACAT | 328967 |
| rs246892136 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61532667 | TAAGAGCTGGAGGAG[A/G]GGGAGAAATGCTTTG | 328967 |
| rs246903346 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61498587 | ACTGCTGATATTGTC[C/T]TTCTGGGCTCCTCCT | 328967 |
| rs246927505 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61536196 | CAGGCAGAGAGATAA[A/G]AAACAGAACAGTTTA | 328967 |
| rs247000019 | in-del | -/A | | | intron-variant | Arhgef37 | Mm_Celera | 18:61529142 | AAACACATGTAAATG[-/A]AAAAAATTAAGAAGG | 328967 |
| rs247000567 | snp | C/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61502206 | GTCAGATGCCGCGTG[C/G]AAAACCTCAGAACAC | 328967 |
| rs247037262 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61514087 | attcataggcaggct[C/T]cgttttccaggattt | 328967 |
| rs247043628 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61506364 | AGTCTCTGCAGCTGG[C/T]ACCTCTGTAGCATAT | 328967 |
| rs247058297 | snp | A/G | | | downstream-variant-500B | Arhgef37 | Mm_Celera | 18:61493447 | GCCCCTTGTGGGTGG[A/G]ACCATCTCTGGGCTG | 328967 |
| rs247163416 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61519013 | GAGAAATGGCTTAGT[A/G]GTTCATAGAAATAAT | 328967 |
| rs247177034 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61508250 | ggcggaggcggaggc[A/G]ggaggatctcagtaa | 328967 |
| rs247248288 | snp | G/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61503065 | AAACATGGGTCCCCA[G/T]GACTCCAGCAGAAAG | 328967 |
| rs247324022 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61512376 | GTCAGTGCTCTTAAC[C/T]GCTGAGCCATCTCTC | 328967 |
| rs247325567 | snp | C/T | | | intron-variant, downstream-variant-500B | Arhgef37 | Mm_Celera | 18:61504743 | GCTTAAACTGTGGAT[C/T]GCAGTCCATATAGGG | 328967 |
| rs247381300 | snp | G/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61495389 | TTTGGGGGGGTTTTA[G/T]GACAGGGTTTATGGC | 328967 |
| rs247421828 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61495735 | TACTGAGGAAGCAGA[C/T]GGACGAAGGCCCATG | 328967 |
| rs247443265 | in-del | -/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61495351 | TTGTTTTGTTTTTTG[-/T]TTTTTTTTTGGGGTT | 328967 |
| rs247490000 | in-del | -/TATATATA | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61519894 | TGGCATATATATATA[-/TATATATA]TATATATTAGATAGC | 328967 |
| rs247533561 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61535522 | GTTTCGCGATCTCCC[C/T]AGTCCCACTCACATA | 328967 |
| rs247595172 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61527393 | AGAAAACTAAGAAAC[C/T]AGTCAATCAAACAAA | 328967 |
| rs247595409 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61526525 | AGCCAGAGAGAAGGT[A/G]GTGCCTCTCTCTCTG | 328967 |
| rs247597578 | snp | A/G | | | utr-variant-5-prime, intron-variant | Arhgef37 | Mm_Celera | 18:61536508 | ACTTGCACCCGCTGG[A/G]CTCCAGCTGCCCGGC | 328967 |
| rs247651724 | snp | C/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61520442 | GGATTTTGAAGCATC[C/G]ATCTTAATAATTGCC | 328967 |
| rs247651777 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61527056 | ATCCTGGCGCTGTTG[A/G]GGGGTGGAGGAGGTA | 328967 |
| rs247653961 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61528098 | CCTAGGACACACATG[A/G]TAAAAGAAGGGAGCC | 328967 |
| rs247682192 | snp | G/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61517119 | CCTCCAAGAAAGAAA[G/T]AAATGTAACTGGCTT | 328967 |
| rs247708102 | snp | A/C | | | intron-variant | Arhgef37 | Mm_Celera | 18:61507025 | GGCTGGGAACTGTTC[A/C]GACTGCTTGGTGCCC | 328967 |
| rs247742337 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61523637 | TTCATAGCTATCCTC[A/G]GCCTCTATGGCTAAG | 328967 |
| rs247821651 | snp | A/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61499134 | TACACATAAAGGTAC[A/T]TAAGTAACTATTATA | 328967 |
| rs247838004 | snp | A/C | | | upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61538219 | CATTTGTTTCATTTA[A/C]AATTCAAAAGCGTAT | 328967 |
| rs247956369 | snp | G/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61530039 | CTCAAGCTCAGAGGG[G/T]TCTGAGATTGAAATT | 328967 |
| rs248026462 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61530748 | TAGACACAGGGGAAA[C/T]TGTAATCAAGATACA | 328967 |
| rs248033453 | in-del | -/A | | | intron-variant | Arhgef37 | Mm_Celera | 18:61525239 | AATAAAAAATAATTT[-/A]AAAAAAAAGAAATGT | 328967 |
| rs248066501 | in-del | -/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61508897 | AGGGGACCAGGGGGC[-/T]TTAGGGTCGTGGCCC | 328967 |
| rs248091448 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61524287 | CTGGCGCCACTACAA[C/T]GATAAAGATGTAGAC | 328967 |
| rs248122507 | in-del | -/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61522455 | CTGACATGCCCAGAC[-/T]TTCCCCTCGCTGATT | 328967 |
| rs248169147 | in-del | -/TGTTTT | | | intron-variant | Arhgef37 | Mm_Celera | 18:61519708 | ATGCTCAGGGTTTTC[-/TGTTTT]TGTTTTTGTTTTTTG | 328967 |
| rs248176947 | in-del | -/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61511156 | ACACACTCACACACA[-/T]AATACACATACTCTC | 328967 |
| rs248267300 | snp | G/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61530359 | CAGGCCATGAGGTTT[G/T]CGAAGCCAGTGACTT | 328967 |
| rs248428370 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61534663 | AGCAGAATCAACCGA[A/G]GCACTGTTTGCTGCA | 328967 |
| rs248461485 | snp | A/G/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61531385 | TGGAAGTCAGGACTC[A/G/T]GCTAGCAGCCTTCAG | 328967 |
| rs248719049 | in-del | -/GTCGCC | | | cds-indel, intron-variant | Arhgef37 | Mm_Celera | 18:61536439 | TCCTGGCGGCATCCT[-/GTCGCC]GTCGCCGGGCTGGAC | 328967 |
| rs248782244 | in-del | -/CTC | | | intron-variant | Arhgef37 | Mm_Celera | 18:61497653 | TCTAGTTAACTCCTA[-/CTC]CTCCTTCCTATGTAA | 328967 |
| rs248834089 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61508461 | GCACATCCACACACA[C/T]CTCTTTCCCTCCCAG | 328967 |
| rs248954490 | snp | A/G | | | intron-variant, upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61513343 | AAACTACACATTTAC[A/G]GTCACTTGATCTTTG | 328967 |
| rs249002138 | snp | A/G | | | intron-variant, upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61514021 | AGAAAATGCATCTCC[A/G]TCCTTTCTCCTTCAT | 328967 |
| rs249024500 | in-del | -/AAAAAAC | | | intron-variant | Arhgef37 | Mm_Celera | 18:61506655 | TTAGAGGAGCAGTTA[-/AAAAAAC]AAAAAACAAAAAACA | 328967 |
| rs249051915 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61514626 | ACTGTTGTCTACTTC[C/T]ACCATGTTCTGGGAA | 328967 |
| rs249051979 | snp | G/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61506641 | AATCTCTCTACAACT[G/T]AGAGGAGCAGTTAAA | 328967 |
| rs249115353 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61525416 | GGCTGCTCTTCCAGA[A/G]GTCCTAAGTTTGACT | 328967 |
| rs249151853 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61518722 | ACACGCAACATCTGC[A/G]CTTTGTTCTGCAGGC | 328967 |
| rs249305210 | in-del | -/CC | | | intron-variant | Arhgef37 | Mm_Celera | 18:61496339 | CCAAACCCTTCAGTG[-/CC]CTAGAGATTGAGCAC | 328967 |
| rs249337814 | snp | G/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61516780 | TTATTTCTCTGATTT[G/T]GGGGATTTCCTTCCA | 328967 |
| rs249346591 | snp | G/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61495384 | GGGGTTTTGGGGGGG[G/T]TTTATGACAGGGTTT | 328967 |
| rs249367252 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61512654 | CCATATTTTACTCCC[C/T]TCCCCATCCACCCCT | 328967 |
| rs249391175 | snp | C/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61517947 | CAAGCAGCCTGGGCA[C/G]ACCCCAGCAGGATCA | 328967 |
| rs249443257 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61515834 | GCTAGGTTATCTAAT[C/T]CCACGTGGTCAGCCC | 328967 |
| rs249509143 | snp | A/C | | | intron-variant | Arhgef37 | Mm_Celera | 18:61508327 | GCTACACAGAGAAAC[A/C]CTGTCTCGAACAATA | 328967 |
| rs249517476 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61509930 | ACTCTAGAACAGCAG[C/T]CAATGCTCTTACGCA | 328967 |
| rs249548104 | in-del | -/AC/ACC/CC | | | intron-variant | Arhgef37 | Mm_Celera | 18:61503979 | CACTGTCTCATCACT[-/AC/ACC/CC]CCCCCCCCCCCGCCA | 328967 |
| rs249572743 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61509040 | TGATAATCCCTGATC[C/T]GTACAAAGTCCAGCG | 328967 |
| rs249584197 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61535375 | TGGTTGGCCAGCAAG[C/T]CTCGGGGATACCTTT | 328967 |
| rs249639816 | snp | C/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61506284 | GAAGCTACCTCTAGC[C/G]CCCAGTTTTGTGGCT | 328967 |
| rs249694039 | snp | C/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61516399 | aaggtttggtgacat[C/G]ctgcactggcaagga | 328967 |
| rs249700496 | snp | A/G | | | upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61538197 | AACAAACAAGCAAAC[A/G]AAAATACATTTGTTT | 328967 |
| rs249710371 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61497507 | AGCACCTCACTACAC[C/T]ATGCCCTCTCTAGTC | 328967 |
| rs249762952 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61524038 | TCAATCCAATTGTAA[A/G]GTAGACCTCTCATTC | 328967 |
| rs249833400 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61515938 | GTATGTGTGTGCATA[C/T]ATATACATGTGTGTG | 328967 |
| rs249844013 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61532494 | TGTTCACCCCCATGC[A/G]TTAATGTTGCTCCCA | 328967 |
| rs249914711 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61532942 | CAGACAGAACTAACT[A/G]AATATCATGGACTAT | 328967 |
| rs249934386 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61528872 | TGCTGTGAAATAACT[A/G]CATACATGTAGTATG | 328967 |
| rs249988691 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61522787 | TATCTGGGGCCATAT[C/T]GCTCTTGGGGAAGAC | 328967 |
| rs249996352 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61528847 | TTACGCAACCCATCA[C/T]GTGATAAAATGCTGT | 328967 |
| rs250044356 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61498832 | TACTACTTCCCCACA[A/G]ACATGTTTTCAGAGT | 328967 |
| rs250070770 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61508599 | GAGTTTTGGATCTAG[A/G]AATGCTGTCCCTGAA | 328967 |
| rs250228851 | in-del | -/CCCACACTT | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61511198 | CGCTCTCACACATAC[-/CCCACACTT]ACACACACACATACA | 328967 |
| rs250335701 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | Arhgef37 | Mm_Celera | 18:61536748 | CAGATCCCCTCGTGG[A/G]CCTTCCTGCTGACAA | 328967 |
| rs250462499 | in-del | -/A | | | intron-variant | Arhgef37 | Mm_Celera | 18:61527912 | CTGAAAATTAACTGG[-/A]AAAAAATGAGATTTT | 328967 |
| rs250516445 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61518394 | ACAGATGGTTGTGAG[C/T]CACCATGTTGTTGCT | 328967 |
| rs250549526 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61506040 | CTTTGGCCATGTGCA[C/T]GCTCTACCGAAGCTA | 328967 |
| rs250592141 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61509642 | AAGTATCAACTTCCT[C/T]TAAATAGTTTAGCAT | 328967 |
| rs250713846 | snp | A/G | | | intron-variant, downstream-variant-500B | Arhgef37 | Mm_Celera | 18:61504650 | AGAGGCTGGGTAGGG[A/G]GCTGGAGGCCCACAG | 328967 |
| rs250766619 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61495926 | TCCTGGAGACTCCGT[C/T]TACATCTACCAGAGC | 328967 |
| rs250933746 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61521754 | GAAGCGGAGGGAGTG[A/G]TTTGAGCTGGGGTCT | 328967 |
| rs250941195 | snp | G/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61535464 | TTTTTAAGTGGGTGC[G/T]GAAGATCCAATTTCC | 328967 |
| rs250999545 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61527249 | CCTGGAACTCATTTT[A/G]TAGACCAGGCTGGCC | 328967 |
| rs251015237 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61521228 | CAGTGTCTGTTCTGA[A/G]CATGTGAGACCTTTT | 328967 |
| rs251022756 | snp | A/C | | | intron-variant | Arhgef37 | Mm_Celera | 18:61516234 | acacatacacacaca[A/C]TCTCTTTaatataga | 328967 |
| rs251066409 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61496111 | GGGAACTGTACACCT[C/T]CCCAGACACTGGCTC | 328967 |
| rs251124317 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61518887 | tttagttgtggaaag[C/T]gagacgtttaatatt | 328967 |
| rs251198960 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61526670 | CTCTACTCGTTGTGT[C/T]TAGATGTTAAAACTG | 328967 |
| rs251236910 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61526577 | GCTGCACCTCTCCCC[A/G]GCTCCATCTGTAGCA | 328967 |
| rs251250090 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61527609 | AACAGACAGGCCTCC[C/T]GGGGTTCCCCATTCG | 328967 |
| rs251271047 | in-del | -/TTTG | | | intron-variant | Arhgef37 | Mm_Celera | 18:61495358 | GTTTTTTGTTTTTTT[-/TTTG]GGGTTTTGGGGTTTT | 328967 |
| rs251286863 | in-del | -/A | | | intron-variant | Arhgef37 | Mm_Celera | 18:61501566 | CTGGACATGGGGGAG[-/A]GTGTGCAGGAGAGCG | 328967 |
| rs251292228 | snp | C/T | | | upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61538946 | TACAGAGAAACCCTG[C/T]CTCGAAAAAAAAAGT | 328967 |
| rs251319905 | snp | G/T | | | intron-variant, upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61514069 | ACTGACTTTCCCCAG[G/T]TCATTCATAGGCAGG | 328967 |
| rs251349086 | snp | A/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61530070 | TGTGTCTGAATCACC[A/T]TGTAAGCCTGCCCCT | 328967 |
| rs251381225 | snp | A/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61497360 | TATACGGATGGATAC[A/T]TGGGTTCTTATAAAT | 328967 |
| rs251431645 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61519960 | ATTTTCTTAGGTAAA[A/G]AGAAGTTGTGAGTGG | 328967 |
| rs251487619 | snp | A/C | | | intron-variant | Arhgef37 | Mm_Celera | 18:61520587 | GAACTACACAGAGAA[A/C]CCTGTCTCAAAAAAA | 328967 |
| rs251488973 | snp | A/C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61511197 | ACGCTCTCACACATA[A/C/T]CCCACACTTACACAC | 328967 |
| rs251613565 | snp | G/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61531229 | TGTTGTTGTTAAACT[G/T]GAAAGCTAGTGTGAT | 328967 |
| rs251647816 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61509039 | TTGATAATCCCTGAT[C/T]TGTACAAAGTCCAGC | 328967 |
| rs251708659 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61509677 | ATAGATAAGAAGATA[C/T]TGATGTGTTAACTCT | 328967 |
| rs251949390 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61515058 | AGAAAGGCTGGCCCG[A/G]CTTCACATCACGCCA | 328967 |
| rs252011029 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61515651 | GGATTAAAGGCGTAC[A/G]CCACCACACCCGGCT | 328967 |
| rs252032956 | in-del | -/GAAAA | | | intron-variant | Arhgef37 | Mm_Celera | 18:61533894 | TTCCTGAAGAAGAAG[-/GAAAA]AAAAAAAAAGACTCC | 328967 |
| rs252043999 | in-del | -/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61525236 | ATCAATAAAAAATAA[-/T]TTTAAAAAAAAGAAA | 328967 |
| rs252099642 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61507191 | TCCCCACCGAACTTG[C/T]GCTCACCCGGGATAC | 328967 |
| rs252180767 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61509578 | ACACTAAATAAATAA[A/G]TGAGTGTAAAAGTAC | 328967 |
| rs252203344 | snp | C/T | | | synonymous-codon, utr-variant-5-prime | Arhgef37 | Mm_Celera | 18:61508775 | CAGCAGGAGGGGGTA[C/T]TTGGTAATCCTCTGT | 328967 |
| rs252251619 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61513012 | GTCAGCTGCTTCTGT[C/T]CATTGGTTGGGTGCA | 328967 |
| rs252297663 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Arhgef37 | Mm_Celera | 18:61536675 | TCCGCTGGTCCCGGG[C/G]CGGGCAGCACCTCAC | 328967 |
| rs252405845 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61524940 | TCAGTGCGTCCCTGC[C/T]CCTTTCCAGCCACCA | 328967 |
| rs252513093 | snp | A/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61517471 | CTACACAGAAAAATC[A/T]TGTCTGGAAAAACAA | 328967 |
| rs252565172 | snp | A/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61514493 | TAGGCATCTCACCTA[A/T]GTTTCTGCTTCTCTG | 328967 |
| rs252660631 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61507115 | GTGCTTCTCTGTGGT[C/T]CCTCCCTCTCAGCTT | 328967 |
| rs252682262 | snp | A/G | | | synonymous-codon | Arhgef37 | Mm_Celera | 18:61507318 | CTGCTCCACTTTGGT[A/G]TACTTTAAGGCTGCG | 328967 |
| rs252727197 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61507969 | TCTTCCAGAGGACCT[A/G]GGTTTGGTTCTTAGC | 328967 |
| rs252775285 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61528165 | acaataaataaataa[A/G]taagtaagtaaataa | 328967 |
| rs252823528 | in-del | -/TTTGGTTC | | | intron-variant | Arhgef37 | Mm_Celera | 18:61506173 | TGCAGTGAACCTGGG[-/TTTGGTTC]CTAGCAACCACAAGG | 328967 |
| rs252876929 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61530271 | AGCGCCCAGAGATGC[C/T]CCTGTCTTCTACCTA | 328967 |
| rs252949752 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61509968 | AGGTCAAGGGCCGCT[A/G]GGGAGAGGCTCCGGC | 328967 |
| rs252987164 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61503168 | GGAGGGGGCTGTCCC[C/T]ACTCCTCCAGAGCAA | 328967 |
| rs253056932 | snp | C/T | | | utr-variant-3-prime | Arhgef37 | Mm_Celera | 18:61494286 | CCCTGGAACCGCCTC[C/T]GAGTTTGTACACACA | 328967 |
| rs253104012 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61514418 | GGTTGCCAACTAGTT[A/G]TTGCTTCTAGCATGG | 328967 |
| rs253148403 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61497127 | TGGGGTGAGACTTTG[C/T]AGCTACTATGGGGTC | 328967 |
| rs253155312 | snp | A/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61533911 | AAAAAAAAGACTCCT[A/T]TGAGTTAAGAAGAGA | 328967 |
| rs253185046 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61497882 | ATACAGAGTGAATGG[C/T]GGACTCCCGCTTATC | 328967 |
| rs253212694 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61534958 | GAGGACCTGAGTTCA[A/G]TTCCCCCTCGCCAAT | 328967 |
| rs253218929 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61523191 | ACAACCATCTGTAAC[C/T]CTGGCTCCTGGGAAT | 328967 |
| rs253266433 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61526584 | CTCTCCCCGGCTCCA[C/T]CTGTAGCATTCTTCT | 328967 |
| rs253282956 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61503832 | ACTGTACAAAATTGC[C/T]TGAGGACTAAGTGAG | 328967 |
| rs253317182 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61501030 | AAACATACAGGTGGC[A/G]GTTGTATGAAAAACT | 328967 |
| rs253358838 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61513671 | GTACTTAAAAAGAAG[-/T]TTTTGTTTTGTTTTG | 328967 |
| rs253406453 | in-del | -/AA | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61533895 | TTCCTGAAGAAGAAG[-/AA]AAAAAAAGACTCCTT | 328967 |
| rs253437935 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61534774 | GCTGGGCAAGAACGG[C/T]GCTGCCAGGTCCCAG | 328967 |
| rs253497797 | snp | G/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61501591 | AGAGCGGCTGGACAT[G/T]GGGGAGGTGTGCAGG | 328967 |
| rs253550714 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61502455 | CACTTTGGCTCATAT[A/G]GCTTGTGAGTCCTGA | 328967 |
| rs253626886 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | Arhgef37 | Mm_Celera | 18:61493676 | ATGTTTGTGCAGGAA[C/T]AGAAACCCTGACTAA | 328967 |
| rs253653164 | in-del | -/TACAGACTCC | | | intron-variant | Arhgef37 | Mm_Celera | 18:61535424 | TCCATGGACTGGAGT[-/TACAGACTCC]CCGGCAAGAACGGCC | 328967 |
| rs253670996 | in-del | -/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61502216 | CGTGGAAAACCTCAG[-/T]AACACCAGTTACTCT | 328967 |
| rs253705437 | snp | C/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61532651 | AGGGGTGGAAAGAGT[C/G]TAAGAGCTGGAGGAG | 328967 |
| rs253710987 | in-del | -/CTACCCTGTGTTT | | | intron-variant | Arhgef37 | Mm_Celera | 18:61496740 | CATGTGAGTGGGGTC[-/CTACCCTGTGTTT]CTGACCTTTCTCTCT | 328967 |
| rs253818722 | snp | G/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61525631 | TCTCATATTAAAATA[G/T]GTTCTTGAGGTCATG | 328967 |
| rs253931748 | snp | C/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61519792 | TTCTGGAAGACCAGG[C/G]CTGTAGATCAAGCTG | 328967 |
| rs253978621 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61498478 | TGTTCCCATGGGACA[A/G]CCCATGAGGTCTGAA | 328967 |
| rs254023639 | in-del | -/TTTTTTTT | | | intron-variant | Arhgef37 | Mm_Celera | 18:61515500 | CCCTGCCTTGGCTTC[-/TTTTTTTT]TTTTTTTTTTTTTTT | 328967 |
| rs254129489 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | Arhgef37 | Mm_Celera | 18:61536967 | GGAACTGAGGCAGGG[A/G]CCGTACAGGAATGTT | 328967 |
| rs254250789 | snp | G/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61496123 | CCTCCCCAGACACTG[G/T]CTCTCAGCTCCACGG | 328967 |
| rs254271584 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61502168 | ATCAAGGGAAAACAA[C/T]GCACTTAGGCCAGGC | 328967 |
| rs254278184 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61528980 | GGCTCAGTGGATAAA[A/G]GAGCATGCCAGCAAG | 328967 |
| rs254322838 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61529888 | GTGAAGGTCAGGAGC[C/T]GTGATAGTAAAAGAC | 328967 |
| rs254362666 | in-del | -/TTA | | | intron-variant | Arhgef37 | Mm_Celera | 18:61519513 | TTGTTTTCATAATTG[-/TTA]TTATTATTGTATTTG | 328967 |
| rs254380512 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61523421 | AGGGGATCCAACATC[C/T]TCACATAGATATACA | 328967 |
| rs254413559 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61526376 | CCTCCAACCCTGCCA[C/T]CCATTCACATTTATC | 328967 |
| rs254476385 | snp | A/C | | | intron-variant | Arhgef37 | Mm_Celera | 18:61520335 | GTTTCTGTCCTATTT[A/C]TGGTGCACCTGTCTT | 328967 |
| rs254543636 | snp | A/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61521168 | GTTTTCATCATTTTT[A/T]TGTCCTACAGTTAAA | 328967 |
| rs254595062 | in-del | -/AGGAAGGA | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61517597 | GGAGGGGAGGGAGGG[-/AGGAAGGA]AGGAAGGAAGGAAGG | 328967 |
| rs254599215 | snp | A/G | | | intron-variant, upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61512286 | ACCCCAGAAGAGGGC[A/G]TTAGATCTCATTACA | 328967 |
| rs254678512 | in-del | -/AAAAAAAAAAATCATTCTTA | | | intron-variant | Arhgef37 | Mm_Celera | 18:61521168 | TTTTCATCATTTTTT[-/AAAAAAAAAAATCATTCTTA]TGTCCTACAGTTAAA | 328967 |
| rs254724653 | snp | A/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61496509 | TTGATGTTATTCATA[A/T]CCCATACCGGTCATC | 328967 |
| rs254787238 | snp | A/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61532870 | TTTTTTCCCCAGGGG[A/T]GTGGCTAATGGGTGG | 328967 |
| rs254800252 | in-del | -/GA | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61501727 | CTGGACATGGGGGGG[-/GA]GTGTGCAGGAGAGCG | 328967 |
| rs254896110 | snp | G/T | | | upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61537397 | CACAGGTAGGTTCTC[G/T]GTTAGCCATAGCCTC | 328967 |
| rs254975368 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61521994 | ATCATTCTGACGCTT[A/G]GTACCACGGTCAGTT | 328967 |
| rs255037734 | snp | A/G | | | intron-variant, upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61513901 | GGATTTTCTTTCCTG[A/G]CCTCCAAACTTACTT | 328967 |
| rs255135364 | snp | A/C | | | intron-variant | Arhgef37 | Mm_Celera | 18:61529584 | GAAAGAGTTCGTCCT[A/C]GAAACCTCTTGCAGT | 328967 |
| rs255271047 | snp | A/C | | | intron-variant | Arhgef37 | Mm_Celera | 18:61495455 | TGAACTCACAGAGAT[A/C]TGCCTGCCTCTGCCT | 328967 |
| rs255343884 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61524435 | CTGGTGCTGAAGCAG[A/G]TACAGACTTAGTCCC | 328967 |
| rs255344870 | in-del | -/A | | | intron-variant | Arhgef37 | Mm_Celera | 18:61497063 | GGAAGACTAACTGAC[-/A]GGGGTGGGGGGTGTC | 328967 |
| rs255462837 | in-del | -/GA | | | intron-variant | Arhgef37 | Mm_Celera | 18:61501495 | AGCGGCTGGACATGG[-/GA]GGGGGGCAGATTGTG | 328967 |
| rs255511858 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61522261 | GGTCCAGTGACATGC[A/G]TGCAGGCAAAACATT | 328967 |
| rs255525450 | snp | A/G | | | intron-variant, downstream-variant-500B | Arhgef37 | Mm_Celera | 18:61504994 | CACCATCACATTAGG[A/G]CATAGATATGCTTTT | 328967 |
| rs255673459 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61496973 | TCTGCCATTCCAGCC[A/G]CTTCCTCCTGCACCT | 328967 |
| rs255685277 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61509063 | GTCCAGCGCTCTATT[A/G]GCCCTATTCACCCTC | 328967 |
| rs255710644 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61527894 | TTTTATAACTGTGAA[A/G]CAACTGAAAATTAAC | 328967 |
| rs255738173 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61514311 | AAATTGGTTTTGAGA[C/T]GTGAAATGGCTCTCA | 328967 |
| rs255798476 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61506997 | TTTGGAAGAGGCACT[C/T]AGCCTGAGCCTCGGC | 328967 |
| rs255817431 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61515165 | GTCCTGCCTCCGCCA[C/T]CCTGATTTCTCAAGC | 328967 |
| rs255833905 | snp | C/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61525582 | AAAATATTTTATGCT[C/G]TTGAGAACATATTAA | 328967 |
| rs255848140 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61499174 | ATAATCCTGTGCAAC[C/T]CTCGTGTTTAGAATA | 328967 |
| rs255964963 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61496137 | GGCTCTCAGCTCCAC[A/G]GTGCCCTGACCCAGA | 328967 |
| rs256007822 | snp | C/T | | | upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61538834 | GGCTGTGGTGGCGCA[C/T]GCCTTTAATCCCAGC | 328967 |
| rs256067156 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61529931 | CACCTATAAAAACAA[C/T]AGTGGCCAGGAGGGG | 328967 |
| rs256129421 | snp | A/C | | | intron-variant | Arhgef37 | Mm_Celera | 18:61530684 | CTAATGAGAGACAAG[A/C]AGTGGGTGGATCCGG | 328967 |
| rs256150604 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61530936 | CTGATTTCACGTCGT[A/G]TTCATAGGCTTTAGA | 328967 |
| rs256185140 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61527627 | GGTTCCCCATTCGGT[A/G]TATTCATAGTGGCTC | 328967 |
| rs256243426 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61518833 | CACAGCATCTTCTCC[A/G]TATATACAAAGTTTT | 328967 |
| rs256244362 | in-del | -/A | | | intron-variant | Arhgef37 | Mm_Celera | 18:61524007 | GTCCACAGGTTCTGG[-/A]AAAAAAAAAAAAATC | 328967 |
| rs256260853 | in-del | -/ACAG | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61510756 | ACACCACACACACAC[-/ACAG]AGACATACACAGACA | 328967 |
| rs256355944 | snp | A/G | | | downstream-variant-500B | Arhgef37 | Mm_Celera | 18:61493369 | agggagcttcagttg[A/G]ggaaatgcctccatg | 328967 |
| rs256459577 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61509436 | AGGGTTGAGGGCCAG[C/T]GAGATGGCTCAGCAG | 328967 |
| rs256466334 | in-del | -/CACACTCT | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61510880 | ACTCACACACACATA[-/CACACTCT]CACACACTCACACAC | 328967 |
| rs256566208 | in-del | -/A | | | intron-variant | Arhgef37 | Mm_Celera | 18:61507784 | ATAAAAATAAATTTT[-/A]AAAAAGATATTGAAG | 328967 |
| rs256600696 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61523230 | CTCCCTGGCTTCCTC[A/G]GGCGCACACACAGTT | 328967 |
| rs256666618 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61515460 | TTGCCATGTAGCCCA[A/G]GTTAGCCTTGAACTC | 328967 |
| rs256668534 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61524151 | TATTAAACAGTCAGT[A/G]AACCGTTGGCTTTTG | 328967 |
| rs256696716 | in-del | -/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61511241 | ACCAATAGAATAATA[-/G]GGGAGTAAAGCAAAA | 328967 |
| rs256711681 | in-del | -/GGGTGTTTTGCCTAC | | | intron-variant | Arhgef37 | Mm_Celera | 18:61509808 | TTTAGGTGCATTGGT[-/GGGTGTTTTGCCTAC]ATGTATGTCTGTGCA | 328967 |
| rs256882817 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61495184 | ACATCACTTCCCAGG[C/T]ACATTCTTAGCACTA | 328967 |
| rs256968767 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61503126 | TGTTAGGACACACAT[C/T]AAGTTCTGCTGGTAT | 328967 |
| rs257012369 | snp | A/G | | | intron-variant, upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61513937 | GTATAGAGGCAAGCT[A/G]ATTTTAGCATGCTTC | 328967 |
| rs257014601 | snp | A/T | | | utr-variant-3-prime | Arhgef37 | Mm_Celera | 18:61494811 | ACACCTTTTAAGTCC[A/T]TAGGAATGGGGGTTC | 328967 |
| rs257091701 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61519600 | ACTGAAATTAAACTT[A/G]TGTGATACAAATCCC | 328967 |
| rs257120401 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61519584 | CCTTTGCCTCCTGAA[C/T]ACTGAAATTAAACTT | 328967 |
| rs257121793 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61526193 | CAGGGTCTCTCTGTA[C/T]AGCTCTGGCTGTCCT | 328967 |
| rs257174737 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61517763 | AATAAGATTGTATAT[C/T]TGTAACTACTTGTAC | 328967 |
| rs257184349 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61533548 | GTCCCAGGGGATCGA[C/T]AATCTCTTCTTGACT | 328967 |
| rs257190797 | snp | A/C | | | intron-variant | Arhgef37 | Mm_Celera | 18:61520120 | ACTGCCTGAGACCAG[A/C]ACCGCTTCCGGTGTT | 328967 |
| rs257249790 | snp | C/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61526019 | GTGAATACCCAGGGG[C/G]ACCACAGTCGTTGAC | 328967 |
| rs257352199 | snp | A/G | | | downstream-variant-500B | Arhgef37 | GRCm38.p3 | 18:61493352 | CAACTTGACACAGCT[A/G]GAGGGAGCTTCAGTT | 328967 |
| rs257402761 | in-del | -/GA | | | intron-variant | Arhgef37 | Mm_Celera | 18:61496052 | CCCTTTGTAGTTCCT[-/GA]GATGTATTATATCTA | 328967 |
| rs257451598 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61528820 | GTCTATACGTGTATG[C/T]ATAAGTGGAGGTTAC | 328967 |
| rs257487796 | in-del | -/CT | | | intron-variant | Arhgef37 | Mm_Celera | 18:61497936 | GTTCCTGTGGGAAGA[-/CT]CTCTATGCATTACAC | 328967 |
| rs257516475 | snp | C/T | | | upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61537079 | CCACAGTGAGCTGGG[C/T]CCTTCCACAGTGATC | 328967 |
| rs257574401 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61528539 | TCAGAGTGCCCTTTA[A/G]CAGCTGAATGATTGA | 328967 |
| rs257711592 | snp | A/C | | | intron-variant | Arhgef37 | Mm_Celera | 18:61509715 | GGTGGTAGATAGAAT[A/C]TTCATCATATCATCC | 328967 |
| rs257713613 | snp | C/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61519297 | TTTAAGTAAAAAGAC[C/G]CCCTACACTTCTGTC | 328967 |
| rs257747329 | in-del | -/ATCTGGGAGCT | | | intron-variant | Arhgef37 | Mm_Celera | 18:61511256 | GGGGAGTAAAGCAAA[-/ATCTGGGAGCT]GTCCTGGAGCAAGCT | 328967 |
| rs257775158 | snp | A/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61507784 | ATAAAAATAAATTTT[A/T]AAAAAGATATTGAAG | 328967 |
| rs257822685 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61507437 | ATCAAGTTACACCCC[A/G]CAGGATGGTAGATCC | 328967 |
| rs257938901 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61535068 | acaagcacataccta[C/T]agacaggcacactcg | 328967 |
| rs258115643 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61522410 | GAGTGGGGCCACAGG[A/G]ATCAGACACTAGATG | 328967 |
| rs258174351 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61514207 | GTCTGGCTGAGATGA[C/T]AAGAATAGCTGGGAC | 328967 |
| rs258176423 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61509910 | GCTGGGAATCTAACC[C/T]AGGTACTCTAGAACA | 328967 |
| rs258223322 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61532360 | CACTGTCATCCTGGT[C/T]AAAAGCCCGTGCACA | 328967 |
| rs258306998 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61509341 | TGTGACGTCACGTCT[C/T]TAGTCCGATAACAAC | 328967 |
| rs258330807 | snp | G/T | | | synonymous-codon | Arhgef37 | Mm_Celera | 18:61504321 | CTGGAGGACCACAAA[G/T]GTGCACAGGATCTGA | 328967 |
| rs258334151 | in-del | -/CT | | | intron-variant | Arhgef37 | Mm_Celera | 18:61510981 | ACACTCACACACACA[-/CT]CACATACACATGCAC | 328967 |
| rs258339240 | snp | A/G | | | upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61538366 | GCCAGCACTCAGGAG[A/G]CAGAGGCAGGTAGAT | 328967 |
| rs258339303 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61508152 | GGGGCGGTAGCACAC[A/G]CTCTTAATCCCAGCA | 328967 |
| rs258475415 | in-del | -/CACACATA | | | intron-variant | Arhgef37 | Mm_Celera | 18:61510853 | ATACTCACACACACT[-/CACACATA]CACATACACACACTC | 328967 |
| rs258478836 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61502868 | CTAGTAAGTTAAAAA[A/G]GGGGGGGGGGTAATT | 328967 |
| rs258541300 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61533488 | GCTGCTCTTCCAGTG[A/G]ACTCAGGTTTGATTC | 328967 |
| rs258546622 | snp | G/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61503430 | AAAGGGGAGCTGGGG[G/T]TAGCGAGTCAGATGA | 328967 |
| rs258559762 | snp | A/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61535073 | CACATACCTACAGAC[A/T]GGCACACTCGTACAC | 328967 |
| rs258637008 | in-del | -/GA | | | intron-variant | Arhgef37 | Mm_Celera | 18:61502351 | CAGGCAGGAGACTGG[-/GA]GAGAGTCAGGACACT | 328967 |
| rs258795508 | snp | A/C | | | intron-variant, upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61513281 | CATTATATTGGTACA[A/C]AGACAGACATGTTGA | 328967 |
| rs258857738 | snp | A/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61505952 | GGGATTAGAAGAGGC[A/T]TACTGGGCCGGGGTC | 328967 |
| rs258905892 | in-del | -/C | | | intron-variant | Arhgef37 | Mm_Celera | 18:61499305 | ATCACTGGAGATCTA[-/C]AGTCCAAGTCATAAA | 328967 |
| rs259018045 | snp | C/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61497406 | ACATGCAGCTGTGCC[C/G]CCCACTGCATCTGTA | 328967 |
| rs259108533 | snp | A/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61498375 | AAAAATAAAATAAAA[A/T]AAAAATAAACAGTAC | 328967 |
| rs259127870 | snp | C/T | | | upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61538851 | CCTTTAATCCCAGCA[C/T]TTGGGAGGCAGAGGC | 328967 |
| rs259229078 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61518738 | ctttgttctgcaggc[A/G]acctcatgctacaca | 328967 |
| rs259258093 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61517836 | ACAGGAACACAAGGA[A/G]GCTTGGAGCCTTGCT | 328967 |
| rs259292880 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61528804 | TTGCGGTGGTGGGAA[C/T]GTCTATACGTGTATG | 328967 |
| rs259338169 | in-del | -/TATATATA | | | intron-variant | Arhgef37 | Mm_Celera | 18:61520161 | GATTGGGGATATTTG[-/TATATATA]TATATATATATAATA | 328967 |
| rs259357457 | snp | G/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61529803 | TCTGGTGTGTCTGAA[G/T]ACAGCATATTCACAT | 328967 |
| rs259496412 | snp | A/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61527112 | CTGGCCTCATGCTAA[A/T]GGAGAACAATTAGGA | 328967 |
| rs259522417 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61521929 | GAACTGGGGTAGCAC[C/T]ATAGGGGTAAGAGAC | 328967 |
| rs259536920 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61502805 | CCACCACCACACATG[C/T]GCGTTCTATGCCTAT | 328967 |
| rs259562432 | in-del | -/CTCGG | | | intron-variant | Arhgef37 | Mm_Celera | 18:61508168 | CTCTTAATCCCAGCA[-/CTCGG]GAGGCAGAGGCGGAG | 328967 |
| rs259612773 | in-del | -/ATCC | | | intron-variant | Arhgef37 | Mm_Celera | 18:61525868 | CATGGCTAAAAAGAA[-/ATCC]ATCCTACCGTATATA | 328967 |
| rs259623795 | snp | A/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61533025 | GTGGAAGGGGGAGTT[A/T]GGTGTGTGTATGATC | 328967 |
| rs259667576 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61530147 | gcacactcaggtaga[A/G]aggtcagaggtcaac | 328967 |
| rs259680299 | snp | A/C | | | intron-variant | Arhgef37 | Mm_Celera | 18:61499140 | TAAAGGTACTTAAGT[A/C]ACTATTATATCACCA | 328967 |
| rs259696620 | snp | C/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61532767 | AAGATCAAGATAGCC[C/G]ACATTCCAACGTGGG | 328967 |
| rs259770056 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61533134 | ACAGGCTCTCAGTGT[A/G]TAGTGTTGGATGTCC | 328967 |
| rs259806719 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61519690 | TATTTGTGATTATCA[A/G]TAAATGCTCAGGGTT | 328967 |
| rs259840686 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61512625 | TCTTTTTAATTAATT[-/A]ATTTTTTTACATTCC | 328967 |
| rs259908176 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61530829 | CAGAAACAATATAAA[A/G]CAGACATACTATCTG | 328967 |
| rs259970656 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61531672 | TCAAATTCAAGTAAA[C/T]GGAGACATAAAAGAG | 328967 |
| rs259992729 | snp | G/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61500033 | GATGGGGACAACCAT[G/T]CCCTCTACTCCATAC | 328967 |
| rs260031339 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61524803 | TCTCTGCAGCCATTG[A/G]GGGCCATGAGTGGGT | 328967 |
| rs260039383 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61522899 | TTAAGACTGGGGATG[A/G]GGGCTAGTTTGGGGC | 328967 |
| rs260074659 | in-del | -/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61516132 | AAAGAAATATATAAA[-/T]TTTTGATAGAAGGGA | 328967 |
| rs260089064 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61496008 | GCGGCTGGGTAGGGT[A/G]ATTGGGTCCCTGGTG | 328967 |
| rs260089444 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61525308 | TTTTTTTTTTCAAAA[A/G]TTTGAACCAGAGTGA | 328967 |
| rs260137534 | in-del | -/CA | | | intron-variant | Arhgef37 | Mm_Celera | 18:61511024 | ACACTCACACACATG[-/CA]CACACATACATACAC | 328967 |
| rs260153953 | snp | G/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61522314 | AAATCAGTACCGTGT[G/T]GAGACTAAACTGGGA | 328967 |
| rs260216180 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61514075 | TTTCCCCAGGTCATT[C/T]ATAGGCAGGCTCCGT | 328967 |
| rs260333842 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61505870 | CAGACCTCCCAAGCA[A/G]CTTTCCAGAGCCCCC | 328967 |
| rs260337361 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61515951 | tacatatacatgtgt[A/G]tgttacatatataca | 328967 |
| rs260341618 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61535260 | TCCCGTAGGATGGCT[C/T]CCTCAGCCTCTCTCC | 328967 |
| rs260394732 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61526974 | GGAAAGGATCAGCCC[A/G]CCAGGGAAATAAATC | 328967 |
| rs260441701 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61527739 | AGAATTATGACCTGT[A/G]GTGCTCTTCTCCCGT | 328967 |
| rs260583002 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61514361 | ATCTGCCACCATGTG[A/G]GCCTGGCTCCAGAGC | 328967 |
| rs260632440 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61506704 | ATAAACTGTATGTGG[C/T]GGCACAGGCCTGTAA | 328967 |
| rs260650595 | snp | G/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61530202 | ATTTTGTTTGAGGTA[G/T]GGTCTCTTTGTTGTT | 328967 |
| rs260711486 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61521361 | GCTAATACTATGCCA[C/T]TTTACACAAGGGGTC | 328967 |
| rs260911407 | snp | G/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61501535 | GGCTGGACATGGGGG[G/T]GGGTGCAGGAGAGCG | 328967 |
| rs260913110 | in-del | -/AAC | | | intron-variant | Arhgef37 | Mm_Celera | 18:61509351 | CGTCTCTAGTCCGAT[-/AAC]AACATCCCAGGACCC | 328967 |
| rs261003048 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61520873 | GTAGTTAAGAGCATC[A/G]ACTGCTCTTCCAGTG | 328967 |
| rs261126240 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61525227 | TTCCCAAATAATCAA[C/T]AAAAAATAATTTAAA | 328967 |
| rs261175710 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61518147 | GAATAAGTTACCTGA[C/T]GGCCAGCAAGCAACA | 328967 |
| rs261197776 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61525812 | CATGATAGTCCCTGG[C/T]ACATCTGTTTTCCTA | 328967 |
| rs261330437 | snp | A/C | | | intron-variant | Arhgef37 | Mm_Celera | 18:61496877 | ATAATAACCACCATC[A/C]TCTCTATCAGGACAG | 328967 |
| rs261338405 | snp | C/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61510364 | ACAACTGTCACCATA[C/G]TACAAACCAGAGGCC | 328967 |
| rs261356446 | snp | G/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61498504 | CTGAAGTTCATCCCT[G/T]GGCCCTCTAGTGGCC | 328967 |
| rs261388033 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61511313 | GGAACACGGGAGAAT[C/T]GCTTACACTGTCAGG | 328967 |
| rs261436582 | snp | A/G | | | missense | Arhgef37 | Mm_Celera | 18:61504448 | CAGGTCACGCTGCCC[A/G]CATCTAACAGCTTCT | 328967 |
| rs261447792 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61505875 | CTCCCAAGCAACTTT[C/T]CAGAGCCCCCACATA | 328967 |
| rs261459964 | in-del | -/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61530578 | TCTTCTATTTGTTTG[-/T]TTTTGTCTTATTCTA | 328967 |
| rs261475320 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61499663 | GCTTCCGGCAACTGG[C/T]TTTCCCAAAAGGAGA | 328967 |
| rs261517275 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61526764 | TCAGAGAAGCCAGAA[C/T]GGATGTAACTTTAAC | 328967 |
| rs261526794 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61528268 | ACGGTCAGTTGCAAA[A/G]CTACATATGACTCAA | 328967 |
| rs261533089 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61496160 | GACCCAGAGCATCCC[A/G]TACACGTCCTCAGCA | 328967 |
| rs261653713 | snp | A/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61524657 | ATTCATGTGGACATA[A/T]GCGTGCATCTCTGCC | 328967 |
| rs261687352 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61516912 | TCGCCCACATGCCCT[A/G]GAATGTGATCCAATA | 328967 |
| rs261723582 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61498702 | ACCAGTCTGGGGTCG[A/G]TCTGTGTCACCGTCA | 328967 |
| rs261802347 | snp | G/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61534435 | GAGCCCATACAGACT[G/T]TTTTTTAAAGCAGGT | 328967 |
| rs261833989 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61526285 | AGTGCTGGAATCAAA[C/T]GTAAGCACCACCATG | 328967 |
| rs261903207 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61498581 | CCTTCCACTGCTGAT[A/G]TTGTCCTTCTGGGCT | 328967 |
| rs261981763 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61496306 | TAGGGTGGGTGTCAA[A/G]GACTCTGCCCCTGCA | 328967 |
| rs262042361 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61533069 | TACACATGTGAAATT[A/G]TGAAAGATTTTTAAA | 328967 |
| rs262079998 | snp | A/C | | | intron-variant | Arhgef37 | Mm_Celera | 18:61525695 | CTTCCTCCCCATAAA[A/C]GGCAGTCCTTCCCTT | 328967 |
| rs262099632 | snp | A/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61528001 | GGCTGGATCTGTAGC[A/T]CAAATTCATATGCAG | 328967 |
| rs262132279 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61526566 | CTTCTGCACTTGCTG[C/T]ACCTCTCCCCGGCTC | 328967 |
| rs262203634 | snp | C/G | | | missense | Arhgef37 | Mm_Celera | 18:61504432 | GGCTGCCTCCTCCTC[C/G]CAGGTCACGCTGCCC | 328967 |
| rs262215130 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61509226 | ACGTGTGCCCTTGGT[A/G]GCCTTGTGTGGTCCT | 328967 |
| rs262246702 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61501979 | TCTGCAGGAGAAGGG[A/G]CCACGGGGTGCCTGG | 328967 |
| rs262287933 | snp | C/T | | | upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61538299 | ACTGCCAAAAAGACA[C/T]TGTTAGTGTTAAGTG | 328967 |
| rs262320629 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61529434 | GAAACCAAGGACACC[C/T]GGAAGAGAAGAACTC | 328967 |
| rs262359313 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61532763 | GCGGAAGATCAAGAT[A/G]GCCCACATTCCAACG | 328967 |
| rs262376876 | in-del | -/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61515422 | TCCCATCCAGCCAAG[-/T]TTTGGAATTATGAGA | 328967 |
| rs262394645 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61525369 | ACTTTATGCTGGGGG[A/G]CTGGAGATATGGCTC | 328967 |
| rs262525808 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61503447 | AGCGAGTCAGATGAC[A/G]ACAGGGAAGCACAGA | 328967 |
| rs262550461 | in-del | -/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61529964 | CTGGCTGAAGGGCAT[-/G]GGTTGATGAGACCTC | 328967 |
| rs262625557 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61531265 | GTATATACTTGCCCC[C/T]GGGGAGTGGCACTAT | 328967 |
| rs262663855 | snp | A/G | | | intron-variant, upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61513554 | TAGAGGATAAAGTGG[A/G]AAAGAGCCTTGAACT | 328967 |
| rs262695821 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61506212 | AACTCACAACCATCT[A/G]TAATTCCAGTTCCAA | 328967 |
| rs262883305 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61535651 | GCATCAGCCCTTCTG[C/T]TGAGCATCTACTGCG | 328967 |
| rs262896609 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61530409 | CAAGTTCCACTACTA[A/G]CCATACTCTTAAGAT | 328967 |
| rs262965303 | in-del | -/AGGATATGG | | | intron-variant | Arhgef37 | Mm_Celera | 18:61506731 | GTAAGCCCAGACCCT[-/AGGATATGG]AGGCAGGATTATGAG | 328967 |
| rs263027727 | in-del | -/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61519724 | GTTTTTGTTTTTTGC[-/T]TTTTTTGTTTTTGCT | 328967 |
| rs263053839 | in-del | -/TTCCTTCCTTCT | | | intron-variant | Arhgef37 | Mm_Celera | 18:61496471 | TCCCTTCTTCCTTCC[-/TTCCTTCCTTCT]TTCCTTCCTCCCTCC | 328967 |
| rs263070377 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61533285 | ATCCACTAATCGCTC[C/T]AGTGTTTCCTATCTG | 328967 |
| rs263152289 | in-del | -/GGGGGGT | | | intron-variant | Arhgef37 | Mm_Celera | 18:61521475 | GACTAGGTGTGGGTG[-/GGGGGGT]GGGGTGTCTTTTTGA | 328967 |
| rs263166543 | in-del | -/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61519274 | CAGTACTTTCCTTAA[-/T]TTTTTTTTTTAAGTA | 328967 |
| rs263170695 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61525763 | CCACACGTGAGTGAC[A/G]ACCTGTGATCGTGTC | 328967 |
| rs263207995 | in-del | -/C | | | intron-variant | Arhgef37 | Mm_Celera | 18:61502127 | TGGCAGGCCTAGCAT[-/C]CCCTCCCCTTACCTA | 328967 |
| rs263209275 | snp | G/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61516713 | TCTTTGGTCTCTGAA[G/T]TTTTGACATTTGAGG | 328967 |
| rs263227609 | snp | A/G | | | missense | Arhgef37 | Mm_Celera | 18:61504469 | AACAGCTTCTCCTCT[A/G]CTCGATCGAAGTCCA | 328967 |
| rs263243292 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61509183 | CCATGGGCTACTCTG[C/T]CTGCCTGATGCTAGA | 328967 |
| rs263282236 | in-del | -/GGT | | | intron-variant | Arhgef37 | Mm_Celera | 18:61521479 | AGGTGTGGGTGGGGG[-/GGT]GGGGTGTCTTTTTGA | 328967 |
| rs263334440 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61535376 | GGTTGGCCAGCAAGT[C/T]TCGGGGATACCTTTA | 328967 |
| rs263415526 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61516038 | TGGGACCCAGAAGGA[A/G]TTGGAGGCAGAGGAA | 328967 |
| rs263458602 | snp | A/G | | | upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61537445 | CTCACAGTTGGAAGA[A/G]CAAAACACGGTGAAG | 328967 |
| rs263502227 | in-del | -/GA | | | intron-variant | Arhgef37 | Mm_Celera | 18:61501791 | AGAGCGGCTGGACAT[-/GA]GGGGGGGCACCTACC | 328967 |
| rs263523801 | snp | A/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61519208 | AAAATTTACTGCTTG[A/T]CTGGAGTTTCAGTTT | 328967 |
| rs263629074 | in-del | -/TG | | | intron-variant | Arhgef37 | Mm_Celera | 18:61511440 | CTGTATCTTTCTGTC[-/TG]TAACTATACAGAAGA | 328967 |
| rs263733319 | snp | A/G | | | intron-variant, upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61513098 | GATAGGCCCCCTTTT[A/G]CGAGTGCTCCATAGC | 328967 |
| rs263746715 | snp | G/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61518403 | TGTGAGCCACCATGT[G/T]GTTGCTGGGATTTGA | 328967 |
| rs263755224 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61514765 | TTACCTAGCAAAAGC[C/T]ACTGACAGCAACACT | 328967 |
| rs263873959 | in-del | -/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61510406 | AAAGAGATGACTGCA[-/T]TTTTTTTTTAATGTC | 328967 |
| rs263905430 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61521291 | CCCCTGACCAGTGCC[A/G]TCAGAAGCCCTCTAG | 328967 |
| rs263926627 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61535257 | agatcccgtaggatg[A/G]ctccctcagcctctc | 328967 |
| rs264102676 | in-del | -/A | | | intron-variant | Arhgef37 | Mm_Celera | 18:61515727 | AAATACATGAAAAAC[-/A]AAAAAAACAGCTACC | 328967 |
| rs264105081 | snp | A/G | | | synonymous-codon | Arhgef37 | Mm_Celera | 18:61494960 | TGGGTTCCCCTTCTT[A/G]TCTTGGGCCTCTAGG | 328967 |
| rs264110615 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61519256 | TTTGGCTTGGAATTA[A/G]GACAGTACTTTCCTT | 328967 |
| rs264142456 | snp | C/T | | | upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61538397 | TTCTAAGTTTGAGGC[C/T]AGCCTGGTCTACAAA | 328967 |
| rs264267927 | snp | A/C | | | intron-variant | Arhgef37 | Mm_Celera | 18:61516506 | CTTCTGAAAAATATG[A/C]CTTGCAGCAGAGTAA | 328967 |
| rs264337717 | snp | A/C | | | intron-variant | Arhgef37 | Mm_Celera | 18:61521598 | CTGGCCTGAGAACAG[A/C]CACAGACCCTGGTGT | 328967 |
| rs264409006 | snp | C/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61525718 | CTTCCCTTTTATGCC[C/G]ACCCCATTGCACCTA | 328967 |
| rs264421824 | snp | C/G/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61528230 | ACAGAGAAGCTACAT[C/G/T]GGCCCTTGATGCAAT | 328967 |
| rs264442205 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61519518 | TTCATAATTGTTATT[A/G]TTATTGTATTTGAGA | 328967 |
| rs264456443 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61522526 | CTGTGTGGACAGAGC[C/T]GAGGGCAAGCAAGCC | 328967 |
| rs264586095 | in-del | -/TTTT | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61535294 | TACTTACTTACTTAC[-/TTTT]TTTTTTTTTTTTTTT | 328967 |
| rs264605817 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61498990 | CTAATGCTGGGGTTA[A/G]AGGCATGCACCATCA | 328967 |
| rs264620264 | in-del | -/TCTGCTGCTTTTGCC | | | intron-variant | Arhgef37 | Mm_Celera | 18:61502016 | ACCCTCTACTCCCAG[-/TCTGCTGCTTTTGCC]TGCCCACCTTTGTGT | 328967 |
| rs264694824 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61524210 | CAAACAACAGCTCAA[A/G]TTGTTGCTGACATTG | 328967 |
| rs264768104 | snp | A/C | | | intron-variant | Arhgef37 | Mm_Celera | 18:61533381 | CATGGCAGCAGCATG[A/C]CATGATCTTTAAAAC | 328967 |
| rs264821798 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61526893 | GCAAGGAAATGATTG[C/T]GGCCAATCTCAGCCA | 328967 |
| rs264956494 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61528651 | AAACAACCTAGAAAG[C/T]TACTGTCCTCAGTAA | 328967 |
| rs264986257 | snp | A/C | | | intron-variant | Arhgef37 | Mm_Celera | 18:61500058 | CCATACCTGGATCTT[A/C]GCTTCCAGTGACATT | 328967 |
| rs265050937 | snp | A/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61532092 | TCAAAGGAATGCTGT[A/T]GCCTACATAACCCAG | 328967 |
| rs265068145 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61524871 | GGCCTGTGTTACCAC[C/T]GAAGTCCGTGCGGAT | 328967 |
| rs265134243 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61502962 | TTCAACCTCATACTT[C/T]GAAAAGTATGCCTGA | 328967 |
| rs265149459 | snp | C/G | | | intron-variant, missense | Arhgef37 | Mm_Celera | 18:61505633 | TGTCGGGCGCCACCA[C/G]CTGCCTATCAGGGGA | 328967 |
| rs265178433 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61495659 | CAAACCGATGTCTAA[A/G]TTCTCTATGGCTTGT | 328967 |
| rs265189539 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61527767 | CGTTCATATACTGGC[A/G]ATTTCAGAAAATTCA | 328967 |
| rs265216124 | in-del | -/A | | | intron-variant | Arhgef37 | Mm_Celera | 18:61509505 | ATGCTCACATGGTAC[-/A]AGGAGGGAGCTGATT | 328967 |
| rs265277158 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61498439 | CACCCTGTTCTACAG[C/T]GGTTGATGTTCCTAG | 328967 |
| rs265319309 | snp | A/G | | | upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61538565 | CTGCTCTTCCGGTGT[A/G]TCTGAAGAGAGCAAT | 328967 |
| rs265325396 | in-del | -/CCCCCCTG | | | intron-variant, upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61512658 | TTTTACTCCCCTCCC[-/CCCCCCTG]CATCCACCCCTCTGA | 328967 |
| rs265337698 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61529858 | GAAAAGATGGTTCAC[A/G]GAGGGCTATCCAAGG | 328967 |
| rs265463145 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61534394 | TTCCCTGGCTCTCCC[C/T]GGAAGGTTGAAAGGG | 328967 |
| rs265545455 | snp | C/T | | | intron-variant, utr-variant-3-prime | Arhgef37 | Mm_Celera | 18:61505174 | AAAAAGCTTTAGAGC[C/T]CTGCTCTAACCTCAC | 328967 |
| rs265550927 | in-del | -/GGGG | | | intron-variant | Arhgef37 | Mm_Celera | 18:61501753 | AGAGCGGCTGGACAT[-/GGGG]GGGGGGGCAGATTGT | 328967 |
| rs265606352 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61536240 | CAACTTACTTTCCAG[A/G]ACCTTTCTCCCACCC | 328967 |
| rs265617794 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61515192 | AAGCCCGGCCATCAA[C/T]CCCCTCTTGGCAAGC | 328967 |
| rs265634066 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61507748 | TAATAAATAAATAAA[C/T]AAATAAATAAATATT | 328967 |
| rs265648827 | in-del | -/TTT | | | intron-variant | Arhgef37 | Mm_Celera | 18:61535295 | TACTTACTTACTTAC[-/TTT]TTTTTTTTTTTTTAA | 328967 |
| rs265683595 | in-del | -/GGGCCCTCC | | | intron-variant | Arhgef37 | Mm_Celera | 18:61498006 | GCCTCACAAGGAGGT[-/GGGCCCTCC]GATAGAAGGAGCAGT | 328967 |
| rs265739494 | snp | A/C | | | intron-variant | Arhgef37 | Mm_Celera | 18:61526378 | TCCAACCCTGCCATC[A/C]ATTCACATTTATCCT | 328967 |
| rs265758555 | snp | A/G | | | intron-variant | Arhgef37 | Mm_Celera | 18:61517124 | AAGAAAGAAATAAAT[A/G]TAACTGGCTTCTGGT | 328967 |
| rs265774643 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61509331 | TGCACTCAATTGTGA[C/T]GTCACGTCTCTAGTC | 328967 |
| rs265847989 | in-del | -/TTTTTTTTTT | | | intron-variant | Arhgef37 | Mm_Celera | 18:61526162 | CTTTTTCTCCTTTTG[-/TTTTTTTTTT]TTTTTTTTTTTGAGA | 328967 |
| rs265879302 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61521879 | CTTCTAATAGGAATC[C/T]GGTTACTTACAGGGA | 328967 |
| rs265895674 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61513366 | GATCTTTGACAGAGA[C/T]GCCAAAAATATACAA | 328967 |
| rs265971747 | snp | C/T | | | upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61537712 | GCTTGTAGATACGGC[C/T]CTTCCCAGCTCTACC | 328967 |
| rs266010758 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61514093 | aggcaggctccgttt[C/T]ccaggatttatttca | 328967 |
| rs266057041 | snp | C/T | | | downstream-variant-500B | Arhgef37 | Mm_Celera | 18:61493435 | CAAGGGGGAATGGCC[C/T]CTTGTGGGTGGGACC | 328967 |
| rs266113341 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61525425 | TCCAGAAGTCCTAAG[C/T]TTGACTCCCAGCAAC | 328967 |
| rs266198412 | snp | A/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61520313 | GCCCAATTCTGCCCT[A/T]TTTTATGTTTCTGTC | 328967 |
| rs266240457 | in-del | -/TG | | | intron-variant | Arhgef37 | Mm_Celera | 18:61501358 | TCCAACCCACCCCTC[-/TG]TGTGTGTGTGTGTGT | 328967 |
| rs266250590 | snp | C/T | | | intron-variant | Arhgef37 | Mm_Celera | 18:61502200 | CCTTCTGTCAGATGC[C/T]GCGTGGAAAACCTCA | 328967 |
| rs386917758 | in-del | -/GT | | | intron-variant | Arhgef37 | Mm_Celera | 18:61527506 | TGTGTGTGTGTGTGT[-/GT]ATAAAACAAGTTTTG | 328967 |
| rs387070289 | in-del | -/CCT | | | intron-variant | Arhgef37 | Mm_Celera | 18:61497658 | TTAACTCCTACTCCT[-/CCT]TCCTATGTAAGGAGA | 328967 |
| rs387125069 | in-del | -/AGGA | | | intron-variant | Arhgef37 | Mm_Celera | 18:61517653 | GGAAGGAAGGAAGGA[-/AGGA]GAAAGGGAAGGAAGA | 328967 |
| rs387194344 | in-del | -/TTTGAGAGGCT | | | intron-variant | Arhgef37 | Mm_Celera | 18:61503676 | AGCTGATGGTTCCTT[-/TTTGAGAGGCT]CTTGATTATTACGTT | 328967 |
| rs387333078 | in-del | -/T | | | upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61537498 | TCTTTTTTTTTTTTT[-/T]AAAGATTTATTTATT | 328967 |
| rs387421349 | in-del | -/ACACACACACACAC | | | intron-variant | Arhgef37 | Mm_Celera | 18:61501266 | CACACACACACACAC[-/ACACACACACACAC]GTAAAATAAAATACA | 328967 |
| rs387574638 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61513261 | GATAAAAAAAAAAAA[-/A]CCTGCATTATATTGG | 328967 |
| rs387590128 | in-del | -/TACA | | | intron-variant | Arhgef37 | Mm_Celera | 18:61525550 | ACATACATACATACA[-/TACA]AACATCTTTTTTTAA | 328967 |
| rs387621265 | in-del | -/AAATAAAT | | | upstream-variant-2KB | Arhgef37 | Mm_Celera | 18:61538639 | AATAAATAAATAAAT[-/AAATAAAT]CTCTTTTTTTGTTTT | 328967 |
| rs387736007 | in-del | -/GTGTGT | | | intron-variant | Arhgef37 | Mm_Celera | 18:61501398 | TGTGTGTGTGTGTGT[-/GTGTGT]CAGGAAGAAGAAATG | 328967 |
| rs387874862 | in-del | -/CACACA | | | intron-variant | Arhgef37 | Mm_Celera | 18:61516223 | ACACACACACACACA[-/CACACA]TACACACACACTCTC | 328967 |
| rs578446321 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61521165 | ACTGTTTTCATCATT[C/T]TTTTGTCCTACAGTT | 328967 |
| rs578457745 | snp | C/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61508170 | CTTAATCCCAGCACT[C/G]GGGAGGCAGAGGCGG | 328967 |
| rs578463571 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61513082 | TTGGGAGGGCAGTCA[C/T]GATAGGCCCCCTTTT | 328967 |
| rs578479433 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61529678 | GCAGAGGCCCAGCTT[C/T]GGGGATCTTACAGTT | 328967 |
| rs578497275 | snp | C/T | | | downstream-variant-500B | Arhgef37 | GRCm38.p3 | 18:61493528 | GCCAGTAAAGAACAT[C/T]CCTCCATGGCCTCTG | 328967 |
| rs578553760 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61513152 | GGACCTCCCCTTGAG[C/T]TGGATCCCAGTTTGG | 328967 |
| rs578565914 | snp | A/G | | | downstream-variant-500B | Arhgef37 | GRCm38.p3 | 18:61493593 | AGTCCTGACTTCCTT[A/G]GTGATGAACAGCAAT | 328967 |
| rs578568837 | snp | G/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61506749 | ATATGGAGGCAGGAT[G/T]ATGAGGATGGCATAG | 328967 |
| rs578587600 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61520691 | TGAGTTCGAGGCCAG[C/T]CTGGTCTACAGAGTG | 328967 |
| rs578692169 | snp | A/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61529709 | AAGAGCACTGACTGC[A/T]CTTCCAGAGGTCCTG | 328967 |
| rs578783514 | snp | G/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61527204 | TTTTTGGTTTTTCGA[G/T]ACAGGGTTTCTCTGT | 328967 |
| rs578807079 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61534294 | TCTTCTCTTCTCTTC[C/T]CTTCTCTTCTCTTCG | 328967 |
| rs578821228 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61517671 | AGAAAGGGAAGGAAG[A/G]AGGGAAAGAGGGAGG | 328967 |
| rs578826893 | snp | A/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61500237 | GCTCCATGGTACACC[A/T]GGCCTTAGCCATTTG | 328967 |
| rs578828012 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61510968 | TCACACACACATGCA[C/T]ACTCACACACACACA | 328967 |
| rs579019441 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61517679 | AAGGAAGAAGGGAAA[A/G]AGGGAGGGAAGAAGA | 328967 |
| rs579034445 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61510800 | ACATATACACACATA[C/T]ACATGCACACTTGCG | 328967 |
| rs579038175 | snp | A/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61525554 | ACATACATACATACA[A/T]ACATCTTTTTTTAAA | 328967 |
| rs579070993 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61535274 | TCCCTCAGCCTCTCT[C/T]CACCTTACTTACTTA | 328967 |
| rs579077629 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61500247 | ACACCAGGCCTTAGC[C/T]ATTTGGAATCCTCAG | 328967 |
| rs579124322 | snp | A/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61525882 | AATCCATCCTACCGT[A/T]TATATCAAAGCCTGG | 328967 |
| rs579139830 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61510916 | ACACATACATACATA[C/T]ACACTCACTCTCACA | 328967 |
| rs579358542 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61520821 | AACAAAACCAAACAA[A/G]CAAAAACAAAAGACA | 328967 |
| rs579395112 | snp | C/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61508080 | GCATGTGGTGCACGG[C/G]GTACACGGAGGCAAA | 328967 |
| rs579461857 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61529351 | ACCAGAGATGCCTGC[C/T]TTCCTGTGCCGAGGA | 328967 |
| rs579559848 | snp | G/T | | | intron-variant, upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61513675 | TTAAAAAGAAGTTTT[G/T]GTTTTGTTTTGTTTT | 328967 |
| rs579609376 | snp | A/G | | | utr-variant-3-prime | Arhgef37 | GRCm38.p3 | 18:61494281 | CTCTTCCCTGGAACC[A/G]CCTCCGAGTTTGTAC | 328967 |
| rs579800237 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61508184 | TCGGGAGGCAGAGGC[A/G]GAGGCGGAGGCGGAG | 328967 |
| rs579825753 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61522494 | AGCTCGGGAGCCAGT[C/T]CTGCGGTAAGCACAG | 328967 |
| rs579882737 | snp | A/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61508085 | TGGTGCACGGCGTAC[A/T]CGGAGGCAAAACACC | 328967 |
| rs579910786 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61533981 | TCTCTCCCTCTCTCT[C/T]CCTCTCTCTTCCCCT | 328967 |
| rs579928048 | snp | G/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61516144 | TAAATTTTGATAGAA[G/T]GGAAATAGTAAAATG | 328967 |
| rs579934475 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61496058 | GTAGTTCCTGAGATG[C/T]ATTATATCTAGCTGA | 328967 |
| rs580022618 | snp | A/G | | | upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61538434 | TCCAGGACAGCCAGG[A/G]CTATACAGAGAAACC | 328967 |
| rs580030577 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61501709 | GATTGTGCAGGAGAG[C/T]GGCTGGACATGGGGG | 328967 |
| rs580030906 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61519867 | GGATTAAAGATGTGC[A/G]CCATCACTAACTGGC | 328967 |
| rs580114284 | snp | C/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61519911 | TATATATATATATTA[C/G]ATAGCAATATACTCC | 328967 |
| rs580157585 | snp | C/T | | | upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61538853 | TTTAATCCCAGCATT[C/T]GGGAGGCAGAGGCAG | 328967 |
| rs580161499 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61504082 | TGGCCTAGAGTCCTG[A/G]CCTCTGCCTCCACAA | 328967 |
| rs580219360 | snp | A/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61511057 | CACACACTCACACAC[A/T]CACACACATACATAC | 328967 |
| rs580363095 | snp | C/T | | | upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61537795 | CCTCACTATATAGTC[C/T]AGGCTGGTGTCAGAC | 328967 |
| rs580370069 | snp | A/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61511071 | CTCACACACATACAT[A/T]CACACACTCACACAC | 328967 |
| rs580378691 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61501324 | GGATTGGGAGATAGT[A/G]TTTCTCTCCCCCACC | 328967 |
| rs580415365 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61519146 | GTCCTCTAGAGATAC[A/G]TTAACACATATGACA | 328967 |
| rs580443191 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61529331 | TTTTGTTTCTATACT[A/G]TAAAACCAGAGATGC | 328967 |
| rs580520712 | snp | G/T | | | intron-variant, upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61513434 | TGGTCTAACTGGCTG[G/T]CTGTATGTAGAAGAA | 328967 |
| rs580551250 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61508220 | GGCGGAGGCGGAGGC[A/G]GAGGCGGAGGCGGAG | 328967 |
| rs580641160 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61512689 | CTGTTCCACATCCCA[C/T]ACCTCCTCCCCAACC | 328967 |
| rs580677072 | snp | C/G | | | upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61538991 | AGAGAGAGACAGAGA[C/G]AGAGACAGAGAGAGA | 328967 |
| rs580683284 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61520668 | GGAGGCAGAGGCAGG[C/T]AAATTTCTGAGTTCG | 328967 |
| rs580685208 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61505911 | CTGTAACTAGCACAT[A/G]TGCCATCTGTCCCTG | 328967 |
| rs580771389 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61517665 | GGAAGGAGAAAGGGA[A/G]GGAAGAAGGGAAAGA | 328967 |
| rs580781687 | snp | G/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61499299 | TCCATGATCACTGGA[G/T]ATCTACAGTCCAAGT | 328967 |
| rs580781796 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61525493 | TGTCCTTTTCTGGTG[C/T]ATCTGAACACAGCGA | 328967 |
| rs580798491 | snp | G/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61508893 | TTTTAGGGGACCAGG[G/T]GGCTTTAGGGTCGTG | 328967 |
| rs580859564 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61534273 | CCTTCCCCTTCTCTT[C/T]TCTTCTCTTCTCTTC | 328967 |
| rs580918102 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61510769 | ACACAGAGACATACA[C/T]AGACACATACCCCAC | 328967 |
| rs580973240 | snp | A/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61525546 | ACATACATACATACA[A/T]ACATACAAACATCTT | 328967 |
| rs581146314 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61534009 | CCTCTCTTCTCCTCC[C/T]CTCTCTTCTCTTCCC | 328967 |
| rs581156271 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61496769 | CTCTTGCCATGTTCA[C/T]CCATGTTGTTAGCAT | 328967 |
| rs581220721 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61517559 | AGGGGAGGGAGGGAG[A/G]GAGGGAGGGAACGAG | 328967 |
| rs581311268 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61510870 | ACATACACACACTCA[C/T]ACACACATACACACT | 328967 |
| rs581313514 | snp | A/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61525564 | ATACAAACATCTTTT[A/T]TTAAAATATTTTATG | 328967 |
| rs581359270 | snp | C/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61520720 | TGAGTTCCAGGACAG[C/G]CAGGACTATACAGAG | 328967 |
| rs581426841 | snp | C/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61529546 | TCACCGCTCAGGGTC[C/G]AACGCCCCTGTGCTG | 328967 |
| rs581432855 | snp | A/G | | | intron-variant, upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61512763 | TCTAAACTCCCTGGG[A/G]CCTCCAGTCTCTTGA | 328967 |
| rs581460917 | snp | C/T | | | upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61538884 | GCAGATTTCTGAGTT[C/T]GAGGCCAGCCTGGTC | 328967 |
| rs581466391 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61513015 | AGCTGCTTCTGTTCA[C/T]TGGTTGGGTGCAAAT | 328967 |
| rs581551438 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61529624 | GTGTGGTTTTCTCTC[A/G]AGTCATTGGGGTGCT | 328967 |
| rs581627014 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61520615 | AAAAAACAAAACAAG[C/T]CGGGCGTGGTGGCAC | 328967 |
| rs581634563 | snp | A/G | | | intron-variant, utr-variant-3-prime | Arhgef37 | GRCm38.p3 | 18:61505276 | GGTTCTCAACTCCTG[A/G]TACTTCTTAGTGTTG | 328967 |
| rs581676607 | snp | C/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61508171 | TTAATCCCAGCACTC[C/G]GGAGGCAGAGGCGGA | 328967 |
| rs581682902 | snp | A/C | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61529705 | AGTTAAGAGCACTGA[A/C]TGCTCTTCCAGAGGT | 328967 |
| rs581788095 | snp | A/G | | | intron-variant, upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61513083 | TGGGAGGGCAGTCAT[A/G]ATAGGCCCCCTTTTA | 328967 |
| rs581857050 | snp | C/T | | | downstream-variant-500B | Arhgef37 | GRCm38.p3 | 18:61493547 | CCATGGCCTCTGCAT[C/T]AGCTCCTGCTTCCTG | 328967 |
| rs581876459 | snp | G/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61521471 | CAAAGACTAGGTGTG[G/T]GTGGGGGGGTGGGGT | 328967 |
| rs581905163 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61525884 | TCCATCCTACCGTAT[A/G]TATCAAAGCCTGGCC | 328967 |
| rs582003670 | snp | A/C | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61510982 | ACACTCACACACACA[A/C]ACATACACATGCACA | 328967 |
| rs582039142 | snp | A/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61510943 | CACACACATACACAC[A/T]TTCACACACTCACAC | 328967 |
| rs582105299 | snp | A/G | | | upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61538191 | GTCTCAAACAAACAA[A/G]CAAACAAAAATACAT | 328967 |
| rs582128779 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61528169 | TAAATAAATAAATAA[A/G]TAAGTAAATAAATAA | 328967 |
| rs582194393 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61534295 | CTTCTCTTCTCTTCT[C/T]TTCTCTTCTCTTCGT | 328967 |
| rs582209858 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61500238 | CTCCATGGTACACCA[A/G]GCCTTAGCCATTTGG | 328967 |
| rs582209968 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61517677 | GGAAGGAAGAAGGGA[A/G]AGAGGGAGGGAAGAA | 328967 |
| rs582234541 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61535445 | CTCCCCGGCAAGAAC[A/G]GCCTTTTTAAGTGGG | 328967 |
| rs582372732 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61517689 | GGAAAGAGGGAGGGA[A/G]GAAGAGAGGGAGGAA | 328967 |
| rs582570804 | snp | A/T | | | intron-variant, upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61513440 | AACTGGCTGTCTGTA[A/T]GTAGAAGAATGAAAA | 328967 |
| rs582680622 | snp | A/C | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61529710 | AGAGCACTGACTGCT[A/C]TTCCAGAGGTCCTGA | 328967 |
| rs582699743 | snp | C/G | | | intron-variant, upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61513162 | TTGAGCTGGATCCCA[C/G]TTTGGGCCTGTTGCT | 328967 |
| rs582704035 | snp | A/G | | | downstream-variant-500B | Arhgef37 | GRCm38.p3 | 18:61493599 | GACTTCCTTGGTGAT[A/G]AACAGCAATGTGGAA | 328967 |
| rs582774213 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61508906 | GGGGGCTTTAGGGTC[A/G]TGGCCCAGCTCTGTC | 328967 |
| rs582776119 | snp | A/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61533081 | ATTGTGAAAGATTTT[A/T]AAAATCTGTTTGTTT | 328967 |
| rs582807437 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61508081 | CATGTGGTGCACGGC[A/G]TACACGGAGGCAAAA | 328967 |
| rs582809237 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61520921 | CAGCAACCACGTGGT[A/G]GCTCACAACCAACTG | 328967 |
| rs582853167 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61529786 | GGGACCCGATGCCCT[C/T]TTCTGGTGTGTCTGA | 328967 |
| rs583014042 | snp | A/C | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61529334 | TGTTTCTATACTATA[A/C]AACCAGAGATGCCTG | 328967 |
| rs583020737 | snp | A/G | | | intron-variant, upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61513788 | ACCATGTGGTTGCTG[A/G]GATTTGAACTCCTGA | 328967 |
| rs583073168 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61525512 | TGAACACAGCGACCA[C/T]ATACATACATACATA | 328967 |
| rs583198086 | snp | A/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61511105 | CATACACACACTCAC[A/T]CTCACATACATACAC | 328967 |
| rs583260866 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61520629 | GCCGGGCGTGGTGGC[A/G]CATGCCTTTAATCCC | 328967 |
| rs583349644 | snp | C/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61504601 | TGTAGGGAGAGGGGA[C/G]CGTGGGAACTGGGAT | 328967 |
| rs583429390 | snp | A/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61529420 | CCTGCCTTGTAAATG[A/T]AACCAAGGACACCCG | 328967 |
| rs583447673 | snp | C/G/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61501742 | GAGTGTGCAGGAGAG[C/G/T]GGCTGGACATGGGGG | 328967 |
| rs583471184 | snp | C/T | | | upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61538870 | GGAGGCAGAGGCAGG[C/T]AGATTTCTGAGTTTG | 328967 |
| rs583486038 | snp | A/C | | | intron-variant, upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61512757 | CTGACCTCTAAACTC[A/C]CTGGGGCCTCCAGTC | 328967 |
| rs583504956 | snp | A/T | | | upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61538446 | AGGGCTATACAGAGA[A/T]ACCCTGTCTCAAAAA | 328967 |
| rs583510667 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61519868 | GATTAAAGATGTGCG[C/T]CATCACTAACTGGCA | 328967 |
| rs583527976 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61520162 | GATTGGGGATATTTG[C/T]ATATATATATAATAA | 328967 |
| rs583595721 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61522551 | CAAGCCAAGCAGCCC[A/G]TGAACACCTGGGTCT | 328967 |
| rs583620869 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61528628 | GGCTCTCAAGAAATG[A/G]CTGTTAAAAACAACC | 328967 |
| rs583628935 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61511058 | ACACACTCACACACT[C/T]ACACACATACATACA | 328967 |
| rs583786731 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61508190 | GGCAGAGGCGGAGGC[A/G]GAGGCGGAGGCGGAG | 328967 |
| rs583828927 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61533983 | TCTCCCTCTCTCTCC[C/T]TCTCTCTTCCCCTCT | 328967 |
| rs583839259 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61529775 | CCATCTGTAATGGGA[C/T]CCGATGCCCTTTTCT | 328967 |
| rs583841322 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61496063 | TCCTGAGATGTATTA[C/T]ATCTAGCTGACACTG | 328967 |
| rs583843285 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61517496 | AAACAACAAAGAAAA[A/G]GGAAGGAAGGAAGGA | 328967 |
| rs584116353 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61529669 | GGGACTTGAGCAGAG[A/G]CCCAGCTTCGGGGAT | 328967 |
| rs584117036 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61508393 | TTGCACTTAACTCTT[A/G]GTAAACCCTTCCGAC | 328967 |
| rs584324580 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61534284 | TCTTCTCTTCTCTTC[C/T]CTTCTCTTCTCTTCT | 328967 |
| rs584332599 | snp | G/T | | | intron-variant, upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61513018 | TGCTTCTGTTCATTG[G/T]TTGGGTGCAAATATC | 328967 |
| rs584339782 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61517669 | GGAGAAAGGGAAGGA[A/G]GAAGGGAAAGAGGGA | 328967 |
| rs584342194 | snp | A/C | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61500236 | GGCTCCATGGTACAC[A/C]AGGCCTTAGCCATTT | 328967 |
| rs584354934 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61520669 | GAGGCAGAGGCAGGC[A/G]AATTTCTGAGTTCGA | 328967 |
| rs584586243 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61507725 | GACAGCTACAGGGTA[A/G]TTACATATAATAAAT | 328967 |
| rs584587566 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61506315 | TTGGGTTACAGTATG[C/T]TTGTCAGCACACCTA | 328967 |
| rs584659034 | snp | G/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61529707 | TTAAGAGCACTGACT[G/T]CTCTTCCAGAGGTCC | 328967 |
| rs584665966 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61513105 | CCCCTTTTACGAGTG[C/T]TCCATAGCCTTAGTA | 328967 |
| rs584675533 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61500242 | ATGGTACACCAGGCC[C/T]TAGCCATTTGGAATC | 328967 |
| rs584684052 | snp | A/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61525550 | ACATACATACATACA[A/T]ACAAACATCTTTTTT | 328967 |
| rs584808147 | snp | A/C | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61520817 | AAAAAACAAAACCAA[A/C]CAAACAAAAACAAAA | 328967 |
| rs584910380 | snp | G/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61529550 | CGCTCAGGGTCCAAC[G/T]CCCCTGTGCTGCATG | 328967 |
| rs584912544 | snp | A/C/G/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61517571 | GAGAGAGGGAGGGAA[A/C/G/T]GAGGGAGGGAGGAGG | 328967 |
| rs584925796 | snp | A/C | | | intron-variant, upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61512831 | GAAATCCTCTATTGT[A/C]TGTGTGTTGGGGCCT | 328967 |
| rs584935359 | snp | A/C | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61510781 | ACACAGACACATACC[A/C]CACACATATACACAC | 328967 |
| rs585031390 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61517678 | GAAGGAAGAAGGGAA[A/G]GAGGGAGGGAAGAAG | 328967 |
| rs585130928 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61510955 | CACTTTCACACACTC[A/G]CACACACATGCACAC | 328967 |
| rs585181197 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61534010 | CTCTCTTCTCCTCCC[C/T]TCTCTTCTCTTCCCC | 328967 |
| rs585195339 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61497070 | CTAACTGACGGGGTG[A/G]GGGGTGTCCCATCTA | 328967 |
| rs585234202 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61525879 | AGAAATCCATCCTAC[C/T]GTATATATCAAAGCC | 328967 |
| rs585240868 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61510914 | ACACACATACATACA[C/T]ATACACTCACTCTCA | 328967 |
| rs585342084 | snp | A/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61528202 | AAGTAAATAAATAAA[A/T]TTTCTAAATTACACA | 328967 |
| rs585403563 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61527162 | TAGAGAATACCTTGA[A/G]AACAGATTTTTTTTT | 328967 |
| rs585419153 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61521743 | AGTGGTGGCAGGAAG[C/T]GGAGGGAGTGGTTTG | 328967 |
| rs585461594 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61519866 | GGGATTAAAGATGTG[C/T]GCCATCACTAACTGG | 328967 |
| rs585683695 | snp | C/G | | | upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61538844 | GCGCATGCCTTTAAT[C/G]CCAGCATTTGGGAGG | 328967 |
| rs585747385 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61508178 | CAGCACTCGGGAGGC[A/G]GAGGCGGAGGCGGAG | 328967 |
| rs585771240 | snp | A/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61511045 | CATACATACACACAC[A/T]CACTCACACACTCAC | 328967 |
| rs585891642 | snp | C/T | | | downstream-variant-500B | Arhgef37 | GRCm38.p3 | 18:61493564 | GCTCCTGCTTCCTGA[C/T]CTGCTTGAGTTCCAG | 328967 |
| rs585985890 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61517711 | AGGGAGGAATGGAGA[A/G]AAAGAGGGAAGGAGG | 328967 |
| rs586113901 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61529722 | GCTCTTCCAGAGGTC[C/T]TGAATTCAATTCCCA | 328967 |
| rs586116017 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61508214 | GGCGGAGGCGGAGGC[A/G]GAGGCGGAGGCGGAG | 328967 |
| rs586128243 | snp | C/G | | | intron-variant, upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61513415 | CATCTTCAATAAATG[C/G]TGCTGGTCTAACTGG | 328967 |
| rs586209994 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61511114 | ACTCACTCTCACATA[C/T]ATACACACTCTCACA | 328967 |
| rs586300267 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61520973 | TCTGGTGTGTCTGAA[A/G]ACAGCTACAGTGTAC | 328967 |
| rs586336706 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61536387 | CAAGAACAACCTCGC[A/G]CACCTCATCTGTCCA | 328967 |
| rs586351442 | snp | C/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61500749 | AAGGTGTCTGTCTGT[C/G]TGTCAGGGACATCTG | 328967 |
| rs586461903 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61511066 | ACACACTCACACACA[C/T]ACATACACACACTCA | 328967 |
| rs586578109 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61529348 | AAAACCAGAGATGCC[C/T]GCCTTCCTGTGCCGA | 328967 |
| rs586603224 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61528778 | TATAGAAATGAACAT[A/G]AAGGAGCATTTTGCG | 328967 |
| rs586659182 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61525520 | GCGACCACATACATA[C/T]ATACATACATACATA | 328967 |
| rs586692421 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61520663 | ACTTGGGAGGCAGAG[A/G]CAGGCAAATTTCTGA | 328967 |
| rs586768978 | snp | G/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61517521 | GAAGGAAGGAAGGAA[G/T]GAAGGGAGGGAGGGA | 328967 |
| rs586810829 | snp | A/C | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61529421 | CTGCCTTGTAAATGA[A/C]ACCAAGGACACCCGG | 328967 |
| rs586818857 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61512758 | TGACCTCTAAACTCC[C/T]TGGGGCCTCCAGTCT | 328967 |
| rs586832630 | snp | A/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61519877 | TGTGCGCCATCACTA[A/T]CTGGCATATATATAT | 328967 |
| rs586833930 | snp | A/T | | | upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61538939 | AGGACTATACAGAGA[A/T]ACCCTGTCTCGAAAA | 328967 |
| rs586939633 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61496041 | ATTCTCGGGGACCCT[C/T]TGTAGTTCCTGAGAT | 328967 |
| rs586979953 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61534272 | CCCTTCCCCTTCTCT[C/T]CTCTTCTCTTCTCTT | 328967 |
| rs586984026 | snp | C/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61497605 | CATGCTGAGAACTCA[C/G]CCCAGGCATCACAAC | 328967 |
| rs587062585 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61533113 | TTTGTTTGTTTGTTT[C/T]TCAATACAGGCTCTC | 328967 |
| rs587068686 | snp | G/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61515615 | CTCAGAAATCTGCCT[G/T]CCTCTGCCTCCCAAG | 328967 |
| rs587071629 | snp | A/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61510640 | AATATTTTTGAAACA[A/T]ACCTTTGCTCCACCA | 328967 |
| rs587153679 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61534005 | TTCCCCTCTCTTCTC[C/T]TCCCCTCTCTTCTCT | 328967 |
| rs587177306 | snp | G/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61496281 | CCCAACCCTCCAAGG[G/T]TGCTTGAGGTAGGGT | 328967 |
| rs587191329 | snp | A/T | | | upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61538411 | CCAGCCTGGTCTACA[A/T]AGTGAGTTCCAGGAC | 328967 |
| rs587234675 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61520215 | AGATAACATATGAAT[A/G]TTAGGTATATATATA | 328967 |
| rs587371126 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61517659 | AAGGAAGGAAGGAGA[A/G]AGGGAAGGAAGAAGG | 328967 |
| rs587473531 | snp | A/G | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61524452 | ACAGACTTAGTCCCC[A/G]GACCCGGACCCGCTT | 328967 |
| rs587511575 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61529623 | GGTGTGGTTTTCTCT[C/T]AAGTCATTGGGGTGC | 328967 |
| rs587522244 | snp | A/G | | | intron-variant, upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61512996 | TAATTTAACAACAGG[A/G]GTCAGCTGCTTCTGT | 328967 |
| rs587551777 | snp | A/G | | | upstream-variant-2KB | Arhgef37 | GRCm38.p3 | 18:61538879 | GGCAGGCAGATTTCT[A/G]AGTTTGAGGCCAGCC | 328967 |
| rs587560640 | snp | C/T | | | intron-variant | Arhgef37 | GRCm38.p3 | 18:61504602 | GTAGGGAGAGGGGAC[C/T]GTGGGAACTGGGATG | 328967 |