| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs261085538 | snp | C/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141957530 | GAGAAACAAGGTACA[C/T]AGTCCCTTATGTTTG | 75770 |
| rs261088260 | snp | C/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141951886 | TCCTGAGTGTCTGCC[C/T]GCTATACTACTGGAG | 75770 |
| rs261360092 | snp | C/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141994790 | GGTAAAGGAGAGGTA[C/T]CTCAGGCTCCCTTGG | 75770 |
| rs261452754 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | Brsk2, Gm20501 | Mm_Celera | 7:141948486 | CACTCTCCATTGGTC[C/T]TCCCAGATAGTGCTG | 75770 |
| rs261496120 | snp | A/C | | | intron-variant | Brsk2 | Mm_Celera | 7:141957563 | CACCCCTTCCTTCCA[A/C]CACAGGAATTTTCCT | 75770 |
| rs261528600 | snp | A/C | | | intron-variant | Brsk2 | Mm_Celera | 7:142001723 | AAGCAGCCCTCATGT[A/C]CCATGCCACTTTGGA | 75770 |
| rs261537997 | in-del | -/GT | | | intron-variant | Brsk2 | Mm_Celera | 7:141982747 | CCCACTCACCTCCAG[-/GT]CTCTCCTGGTCCCTA | 75770 |
| rs261564627 | snp | A/G | | | intron-variant | Brsk2 | Mm_Celera | 7:141994308 | GAAAGTATTGGCAAA[A/G]ACCATTGCATCATTG | 75770 |
| rs261583682 | snp | A/G | | | intron-variant | Brsk2 | Mm_Celera | 7:141957885 | GTCTCCAGCTTAAAG[A/G]GCATCCTCCCAGACT | 75770 |
| rs261617559 | snp | G/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141960022 | AGGTCAGCCCTGATG[G/T]TTCCATGAACACAGA | 75770 |
| rs261622911 | in-del | -/GGGTT | | | intron-variant | Brsk2 | Mm_Celera | 7:141968464 | GACATGATTTTCATA[-/GGGTT]GGGAGGTCAGGGACT | 75770 |
| rs261811580 | in-del | -/TCC | | | intron-variant | Brsk2 | Mm_Celera | 7:141968717 | TAGGAGCAGTCTCTT[-/TCC]TCTAGCTTCTCTGTG | 75770 |
| rs261835979 | snp | C/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141965539 | CGTGTTGAGAAGGAC[C/T]CCCATGCAGCGCACT | 75770 |
| rs261871159 | in-del | -/AGG | | | intron-variant | Brsk2 | Mm_Celera | 7:141984655 | ATTCCTGTCAAGGGC[-/AGG]AGGACACAGCATCCC | 75770 |
| rs261900413 | snp | A/G | | | intron-variant | Brsk2 | Mm_Celera | 7:141980390 | TTTGGTTGTGAATGG[A/G]TCTTTTGTGGAGGAG | 75770 |
| rs261913690 | snp | C/G | | | intron-variant | Brsk2 | Mm_Celera | 7:142000091 | AGTGCCACGTCCCTG[C/G]TGTTACAGGGAATAT | 75770 |
| rs262009298 | snp | C/G | | | intron-variant, upstream-variant-2KB | Brsk2, Mir3104 | Mm_Celera | 7:141990185 | GGTCACCCAGGGCAG[C/G]CTGTGCTGTGGCTTC | 75770 |
| rs262043375 | snp | C/T | | | upstream-variant-2KB, intron-variant | Brsk2, Gm20501 | Mm_Celera | 7:141949155 | ACAGAGCACCCACGG[C/T]GAATGCAGCAACCCA | 75770 |
| rs262061983 | snp | A/G | | | intron-variant | Brsk2 | Mm_Celera | 7:141955804 | CAGCAGCTGGGAGCC[A/G]GCCCCGCCTGCTGGA | 75770 |
| rs262341324 | snp | A/G | | | intron-variant | Brsk2 | Mm_Celera | 7:141989026 | TTATAAACTGGTCTG[A/G]ACCGAACTAGACTGG | 75770 |
| rs262359224 | snp | A/G | | | intron-variant | Brsk2 | Mm_Celera | 7:141973577 | GCCAGGAGGCATCCG[A/G]GGCTTGCTAGCTCTC | 75770 |
| rs262452029 | snp | C/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141954300 | GAAAGGATGCTTATC[C/T]AAGGTGTGATGCGTG | 75770 |
| rs262456074 | in-del | -/CTGGAGC | | | intron-variant | Brsk2 | Mm_Celera | 7:141973355 | GCGCTCATCAGCTGA[-/CTGGAGC]CAGCATTCAGGTGCA | 75770 |
| rs262532229 | in-del | -/G | | | intron-variant | Brsk2 | Mm_Celera | 7:141965602 | GCTGCTCTGGGTCCT[-/G]GACAGTTCTGAGTCC | 75770 |
| rs262545093 | snp | C/G | | | intron-variant | Brsk2 | Mm_Celera | 7:141955639 | CTGCTGAGCCAGGCT[C/G]ACCAGGGTTCTGAAC | 75770 |
| rs262632604 | snp | C/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141986788 | TTGGTTCAGGTGAGC[C/T]CTGGAGGGTCTGCCC | 75770 |
| rs262651377 | snp | C/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141998294 | CCTGCATAGTGCTGG[C/T]ACTTCTGTTGCCACC | 75770 |
| rs262760271 | snp | C/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141953584 | GTCCCTGTAGATGGG[C/T]CAGGCTGGTGAGGGC | 75770 |
| rs262793868 | snp | A/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141954799 | TCTCTGGTTAGTCAC[A/T]TGAACAGTAGTATAA | 75770 |
| rs262919050 | snp | C/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141966679 | CAAGTGCTGTGGGAG[C/G]TGAGGCCTTGGGTCT | 75770 |
| rs262960285 | in-del | -/TG | | | intron-variant | Brsk2 | Mm_Celera | 7:141980309 | ATGCACATACATGTC[-/TG]TGTATGTGTGTGTGT | 75770 |
| rs263069710 | snp | A/C | | | intron-variant | Brsk2 | Mm_Celera | 7:141972491 | TGTGGGAAATTTCTT[A/C]TGACTTCTTTTCAGT | 75770 |
| rs263275137 | in-del | -/GG | | | utr-variant-5-prime, upstream-variant-2KB | Brsk2, Gm20501 | Mm_Celera | 7:141949808 | GGACGGGCGTGCGCT[-/GG]GGGGGGGCGCGGGGC | 75770 |
| rs263328807 | snp | C/G | | | intron-variant | Brsk2 | Mm_Celera | 7:141982484 | CAGTAGCTGTGGGGT[C/G]AAGGCAGCCATGGGC | 75770 |
| rs263335994 | snp | C/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141964521 | GGGTGTTGGGTCTTA[C/T]GTGGAAACACCCACA | 75770 |
| rs263348093 | snp | A/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141969192 | TGTCTGGTAAGAGAC[A/T]TGGGATACAGGATAG | 75770 |
| rs263445001 | snp | A/G | | | intron-variant | Brsk2 | Mm_Celera | 7:141971191 | AGGGCAGGAGTTGGG[A/G]GGATTAGGCAGGGAG | 75770 |
| rs263573035 | snp | A/T | | | upstream-variant-2KB, nc-transcript-variant | Brsk2, Gm20501 | Mm_Celera | 7:141948699 | AGCCTGGCCGCCATC[A/T]GTTCTCTTCCACCAC | 75770 |
| rs263645370 | snp | C/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141970349 | TTTGTCCAGGCATGA[C/T]AGACACTCTGAGCTT | 75770 |
| rs263729540 | snp | A/G | | | intron-variant | Brsk2 | Mm_Celera | 7:141970059 | CTTGGGAACACTGGC[A/G]GCCAGCTTCCAAGGA | 75770 |
| rs263749836 | snp | C/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141961920 | GGGCGGCGGGGTCCC[C/T]GAACTGTGTATGGTT | 75770 |
| rs263786885 | snp | C/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141982063 | AGATGACAGCTTAGG[C/T]AAAGTGGAGAACTTT | 75770 |
| rs263822351 | snp | A/G | | | intron-variant | Brsk2 | Mm_Celera | 7:141983738 | TGTCCCCCAGTTCTG[A/G]TCCTGGTGTGGTTTC | 75770 |
| rs263863071 | snp | G/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141954698 | ACCATTTCCCTGGCT[G/T]CCCTTCCTTTCTCTG | 75770 |
| rs263910391 | snp | C/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141996355 | GTTGAGACTTAGACA[C/T]TCTCTCCTGTCCCCT | 75770 |
| rs263944011 | snp | C/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141997950 | TCAGCCTGGAACTCC[C/T]ATCCACTTCCCCATG | 75770 |
| rs264003507 | snp | A/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141960720 | GCAGGCTGATGACTG[A/T]CATCCCTGGTTACAT | 75770 |
| rs264102168 | snp | G/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141968493 | CTGGAAGCCTATCGA[G/T]TCGTTTATAATCTGA | 75770 |
| rs264103592 | snp | A/G | | | intron-variant | Brsk2 | Mm_Celera | 7:141954439 | CTGCCCTGCCATAGG[A/G]AGGGCACGAGGGAGA | 75770 |
| rs264348335 | snp | C/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141959522 | GTGATGGCCTTGGGT[C/T]ACTGTTGGGGCATGG | 75770 |
| rs264403752 | snp | G/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141977973 | AGTAGCCCTGGAAGG[G/T]CCTGGGGCCTTGACA | 75770 |
| rs264423524 | snp | C/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141966446 | CTCAGGCTCAGCCTT[C/T]ACTCAGTACTCTGAC | 75770 |
| rs264456559 | snp | C/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141958761 | CCAGGCCTCTTGCTC[C/T]AAACCCCACATCCTA | 75770 |
| rs264542291 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | Brsk2, Gm20501 | Mm_Celera | 7:141948631 | TACACTGTTGACTAG[A/G]GTAGCTTCCATTGAA | 75770 |
| rs264703637 | snp | G/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141960841 | TGGGTCCTGAGCTGA[G/T]GGGTGCCGCTTTCCA | 75770 |
| rs264796938 | snp | C/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141964833 | AGCATTCTGAACACT[C/T]TAGGCTCCTGTCATG | 75770 |
| rs264835711 | snp | A/G | | | intron-variant | Brsk2 | Mm_Celera | 7:141998875 | GGCCCCTCCCCGGGC[A/G]TGGTGGGCTGCATCA | 75770 |
| rs264907246 | snp | A/G | | | intron-variant, upstream-variant-2KB | Brsk2, Mir3104 | Mm_Celera | 7:141992139 | CCTTCCTCGGCCTTG[A/G]AGCTCCGGGTCAGGA | 75770 |
| rs264918355 | in-del | -/TG | | | intron-variant | Brsk2 | Mm_Celera | 7:141959577 | ATGCACACTGGTCCT[-/TG]CGTGTTGCTGGTCCT | 75770 |
| rs264957334 | snp | A/G | | | intron-variant | Brsk2 | Mm_Celera | 7:141956797 | CTGGGCCTGGAATCC[A/G]TTGGCCAGGTAAGGG | 75770 |
| rs264998466 | snp | A/G | | | intron-variant | Brsk2 | Mm_Celera | 7:141977808 | CTACCTGTAGTGAAG[A/G]TCACTATTGCTCAGA | 75770 |
| rs265047475 | snp | A/G | | | intron-variant | Brsk2 | Mm_Celera | 7:141987320 | CCTGGGCCTCTGAGA[A/G]TGCAGCCCCTGCCCT | 75770 |
| rs265110478 | snp | A/G | | | intron-variant | Brsk2 | Mm_Celera | 7:141994002 | TCACAGGGAGGGTTT[A/G]GACATGAGGAAAAAC | 75770 |
| rs265207196 | snp | A/G | | | intron-variant | Brsk2 | Mm_Celera | 7:141996694 | TATCTTGTTTGTGGA[A/G]CAAGTTTAGAGTTGG | 75770 |
| rs265217606 | snp | A/G | | | intron-variant | Brsk2 | Mm_Celera | 7:141984164 | GGCAGGCCCTGTTGG[A/G]TCAGCCTCACTCCAT | 75770 |
| rs265240980 | snp | A/G | | | intron-variant | Brsk2 | Mm_Celera | 7:141952428 | GTGGGCTCACAGCCC[A/G]AGAGGGCCTGTAGGA | 75770 |
| rs265382744 | in-del | -/GT | | | intron-variant | Brsk2 | Mm_Celera | 7:141986630 | CATGTGAGTATCTGC[-/GT]GTGTGTGTGTGTGTG | 75770 |
| rs265395485 | snp | A/C | | | intron-variant | Brsk2 | Mm_Celera | 7:141954514 | CTGAAGCAGGTCCAG[A/C]GCTAACCCTTACAGC | 75770 |
| rs265438268 | snp | C/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141971592 | TTAGACTATGGGACT[C/T]TCATCAGGAAGGATT | 75770 |
| rs265598757 | snp | A/G | | | intron-variant | Brsk2 | Mm_Celera | 7:141965357 | TGACAGTTCAAAGCA[A/G]GAGAATAGGAACTGT | 75770 |
| rs265619382 | snp | G/T | | | intron-variant, upstream-variant-2KB | Brsk2, Gm20501 | Mm_Celera | 7:141950285 | CCGGGTGGGGCCGAG[G/T]GAGGCCGCAGAGCAG | 75770 |
| rs265814204 | snp | A/G | | | intron-variant | Brsk2 | Mm_Celera | 7:141969553 | ATCCTGACTACAGCC[A/G]CGGCTTGGAAACATG | 75770 |
| rs265879416 | snp | A/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141959958 | GGTGAGAGGTTGCTG[A/T]TGCTCACCTCTGGCT | 75770 |
| rs266018961 | in-del | -/G | | | intron-variant | Brsk2 | Mm_Celera | 7:141995725 | TCTTCCAATTGCCAA[-/G]TTGTCAAGCTATCAT | 75770 |
| rs266027216 | snp | C/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141962386 | GGTCTTGCAAGTTGT[C/T]TCTAGTACTGGCCGT | 75770 |
| rs266037919 | snp | C/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141966991 | GTGTCAGTGGGAAGA[C/T]CTTTCCTCAATTAGA | 75770 |
| rs266192600 | snp | A/G | | | intron-variant | Brsk2 | Mm_Celera | 7:141968761 | CACCTGACTGGCCTG[A/G]TGGGTAAAATGCCTC | 75770 |
| rs387327630 | in-del | -/GGCGCGGCG | | | utr-variant-5-prime, upstream-variant-2KB | Brsk2, Gm20501 | Mm_Celera | 7:141949928 | CGTACGGGTGCGGCG[-/GGCGCGGCG]TGGGGGGCGGCGGGG | 75770 |
| rs578450050 | snp | C/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141977519 | TGCATCCCCACTGCC[C/T]GAAGTTATCCCTGGG | 75770 |
| rs578514426 | snp | C/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141965196 | GTAGGTTCTCCTGAT[C/T]GTCTGATGACTTAGT | 75770 |
| rs578682511 | snp | C/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141985837 | CCCCACACCCCCTCC[C/T]CAGCCCTCCTCTTAT | 75770 |
| rs578849794 | snp | A/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141983233 | CTGGGGGGTCTCCAG[A/G]CTGTTAACTTGAGGC | 75770 |
| rs578890584 | snp | C/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141966926 | AAGGGAGAGTAGTCA[C/G]TTCAGTCAATACAAG | 75770 |
| rs579040534 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | Brsk2, Gm20501 | GRCm38.p3 | 7:141948620 | TCACCTAGTAGTACA[C/T]TGTTGACTAGAGTAG | 75770 |
| rs579073098 | snp | A/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141974926 | CCTACTAGTCACTTC[A/G]AGCTGGACAGCAGTT | 75770 |
| rs579227028 | snp | A/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141952882 | AGAGAGAGAGAGAGA[A/G]AGAGAGAGAGAGAGA | 75770 |
| rs579295700 | snp | A/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141974429 | CATGTCACTGGCAGC[A/G]GGGGAGGCAGAACAG | 75770 |
| rs579398000 | snp | C/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141977518 | TTGCATCCCCACTGC[C/T]CGAAGTTATCCCTGG | 75770 |
| rs579841949 | snp | C/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141994958 | TCTCATGTACCCTTA[C/T]GGCTCACACCATGTA | 75770 |
| rs579861313 | snp | A/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141968380 | GTGGGGTGAGGGGAG[A/G]CATGGTCAGCAGGGT | 75770 |
| rs579959493 | snp | C/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141994300 | GGGTAGGGGAAAGTA[C/T]TGGCAAAAACCATTG | 75770 |
| rs580180092 | snp | A/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141980896 | AGGAAGGGCTCTGGT[A/G]ACATGGGGGAAGGGC | 75770 |
| rs580248148 | snp | A/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141953478 | CATGGGTGGAGGGTG[A/G]TAAAGTGAACAGGAG | 75770 |
| rs580305546 | snp | A/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141962957 | GTCAGAAGCTAGACA[A/G]CTGCTGTCCAGAGCA | 75770 |
| rs580478857 | snp | A/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141977639 | AACTAGTGTCCAGAG[A/G]GCAGAGCAGTGTGCC | 75770 |
| rs580661340 | snp | A/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141969608 | GCTGAGAGGTGAGTG[A/G]CTGGGGAGGCCGCTG | 75770 |
| rs580748321 | snp | C/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141973883 | ATACCAGTGACAAGG[C/T]TCAGGAGCAGCCAGG | 75770 |
| rs580789975 | snp | C/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141997545 | CCTGTCTTTGTGACT[C/T]CTATGTGGGGCTGCC | 75770 |
| rs580883607 | snp | C/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141972639 | AGCCAGCTCTGTGCA[C/T]CAGTGATCTCCTGCC | 75770 |
| rs581131223 | snp | C/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141964750 | GTCTCTTTGTGTCTT[C/T]CTTGACATAAAGGTT | 75770 |
| rs581309900 | snp | C/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141985078 | TGTGGCTGGAGAGCA[C/T]TAAAGCTGGACTGAA | 75770 |
| rs581442323 | snp | C/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141963906 | CTCCCCTCCCCTCCC[C/T]TCCCCTCCCTTCCCC | 75770 |
| rs581562811 | snp | A/C | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141982734 | CACACAGCAGCAAGC[A/C]CACTCACCTCCAGCT | 75770 |
| rs581734880 | snp | A/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141952896 | AGAGAGAGAGAGAGA[A/G]AGACCATACTTGCCA | 75770 |
| rs581785629 | snp | A/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141952874 | AGAGAAAGAGAGAGA[A/G]AGAGAGAGAGAGAGA | 75770 |
| rs581935959 | snp | A/C | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141981152 | CTCTTATAAAGGCAA[A/C]CATTTAATTGGGGCT | 75770 |
| rs581964007 | snp | A/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141976856 | ACTGGGTGACCTGGG[A/G]TGCCCTGGCCAGGTG | 75770 |
| rs582272262 | snp | A/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141968477 | ATAGGGAGGTCAGGG[A/G]CTGGAAGCCTATCGA | 75770 |
| rs582381700 | snp | C/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141985855 | GCCCTCCTCTTATAC[C/T]CATGATGAGTGCTGT | 75770 |
| rs582572470 | snp | G/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141967666 | TTTGGGTTCAAATGG[G/T]TCACTTTAGCCTGTA | 75770 |
| rs582767380 | snp | A/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141988934 | GTCTGGACTAGCTCT[A/G]TGTATCTAGCTGTAC | 75770 |
| rs582883147 | snp | A/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141952886 | AGAGAGAGAGAGAGA[A/G]AGAGAGAGAGAGACC | 75770 |
| rs582914336 | snp | C/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141962933 | GAGCATTATAGATTG[C/T]CCCACACTGTCAGAA | 75770 |
| rs582982428 | snp | A/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141974711 | GCCCACACCTCCCTG[A/G]TAATCTGGGGGGGGG | 75770 |
| rs583088348 | snp | A/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141980913 | CATGGGGGAAGGGCA[A/G]GGGTGCATGAAGACC | 75770 |
| rs583362321 | snp | A/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141957835 | GCCTGGTGGGCATGG[A/G]AGAAGGGGACTTACT | 75770 |
| rs583552449 | snp | A/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141995647 | CCCCTAGGGTCTCTG[A/G]AACAGAGATCTAAGA | 75770 |
| rs583664010 | snp | G/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141994642 | AAAAGCCTTTTGGCG[G/T]CCACCTCCTCCTTGA | 75770 |
| rs583705816 | snp | A/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141970782 | GTGTGTGTGTGTGTG[A/T]GTGAGTTGAGATGTC | 75770 |
| rs583914753 | snp | A/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:142000211 | CCATTCTTGGATCTC[A/G]GCCTGTCCCCCTGAT | 75770 |
| rs583952695 | snp | C/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141962582 | ATGTGTGTGTGTGCA[C/T]GTGCACACGCACGCA | 75770 |
| rs584011239 | snp | C/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141963896 | GGGGACTCCCCTCCC[C/T]TCCCCTCCCCTCCCC | 75770 |
| rs584124425 | snp | A/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141977655 | GCAGAGCAGTGTGCC[A/G]AGCTACTACATCACA | 75770 |
| rs584491193 | snp | C/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141963920 | CCTCCCCTCCCTTCC[C/T]CTCCCCTCCCCTCCC | 75770 |
| rs584551321 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | Brsk2, Gm20501 | GRCm38.p3 | 7:141947864 | GCACATCCAAGAGAA[A/G]AGATGCTACACCTGA | 75770 |
| rs584608141 | snp | C/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141973843 | TCACACCTGGATATT[C/T]CTGAATTCCAGTGGA | 75770 |
| rs584676982 | snp | A/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141951381 | CACTGAGCCAAAGGC[A/G]GGTGGGTTTTTTTTT | 75770 |
| rs584725136 | snp | G/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141985079 | GTGGCTGGAGAGCAC[G/T]AAAGCTGGACTGAAG | 75770 |
| rs584910497 | snp | A/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141974765 | ACTGGGTGACCTGGG[A/G]TGCCCTGGCCAGGTG | 75770 |
| rs585122510 | snp | C/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141974428 | TCATGTCACTGGCAG[C/G]GGGGGAGGCAGAACA | 75770 |
| rs585288445 | snp | C/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141982745 | AAGCCCACTCACCTC[C/T]AGCTCTCCTGGTCCC | 75770 |
| rs585436626 | snp | A/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141987148 | GATTCCTCATGTGAT[A/G]CCCTCTGATCTGGGA | 75770 |
| rs585580389 | snp | A/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141952878 | AAAGAGAGAGAGAGA[A/G]AGAGAGAGAGAGAGA | 75770 |
| rs585610990 | snp | C/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141977546 | TGGGGTATTTTTGTA[C/G]ATCACCTGGATCACC | 75770 |
| rs585759728 | snp | C/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141977398 | AGGGAAGAGGCACTG[C/G]CTCCTAGTCTGTGTC | 75770 |
| rs585894088 | snp | C/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141960494 | CTAGATCTTGGCCTA[C/G]TGTCCTAGACATACT | 75770 |
| rs586005010 | snp | A/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141979575 | AGGCCATCCTTGGGA[A/G]GAAGCTGGGTTTTTG | 75770 |
| rs586164023 | snp | C/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141973869 | GTGGAGAGCTGAGCA[C/T]ACCAGTGACAAGGTT | 75770 |
| rs586643796 | snp | G/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141995709 | GGGCTAGGAAGGAAT[G/T]TCTTCCAATTGCCAA | 75770 |
| rs586770834 | snp | C/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141962934 | AGCATTATAGATTGC[C/T]CCACACTGTCAGAAG | 75770 |
| rs586870257 | snp | A/G | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141982693 | CCTGCAGTCTTCTAT[A/G]TACACATGCAGCCCC | 75770 |
| rs586927444 | snp | C/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141963935 | CCTCCCCTCCCCTCC[C/T]CTCCTCTCCTCTTCT | 75770 |
| rs587114140 | snp | C/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141963900 | ACTCCCCTCCCCTCC[C/T]CTCCCCTCCCCTCCC | 75770 |
| rs587291715 | snp | A/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141970784 | GTGTGTGTGTGTGTG[A/T]GAGTTGAGATGTCAT | 75770 |
| rs587432901 | snp | C/T | | | intron-variant | Brsk2 | GRCm38.p3 | 7:141969606 | AGGCTGAGAGGTGAG[C/T]GGCTGGGGAGGCCGC | 75770 |
| rs587455671 | snp | A/T | | | utr-variant-3-prime | Brsk2 | GRCm38.p3 | 7:142003688 | TTTTAAATTAAAATT[A/T]AAAAGTTTAAAAAAA | 75770 |
| rs864266137 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Brsk2 | GRCm38.p3 | 7:141975605 | AGTGCCCAGCCCACA[C/T]GGCAGTGCCTTGCCC | 75770 |