| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs6391371 | snp | A/C | 0.5 | 0 | intron-variant | Daw1 | GRCm38.p3 | 1:83177152 | agtcatcaactgtcc[A/C]tagctcctcaggcag | 71227 |
| rs6391435 | snp | C/T | 0.5 | 0 | intron-variant | Daw1 | Mm_Celera | 1:83177191 | attgtgtttattccc[C/T]cctcagtgctggaac | 71227 |
| rs6392572 | snp | A/G/T | 0.5 | 0 | intron-variant | Daw1 | GRCm38.p3 | 1:83177399 | tatgcatgctgaact[A/G/T]ctgagcnatctttcc | 71227 |
| rs6392588 | snp | C/T | 0.5 | 0 | intron-variant | Daw1 | Mm_Celera | 1:83177406 | gctgaactnctgagc[C/T]atctttccancccAT | 71227 |
| rs6392608 | snp | G/T | 0.5 | 0 | intron-variant | Daw1 | Mm_Celera | 1:83177416 | tgagcnatctttcca[G/T]cccATGCTGAGACAC | 71227 |
| rs6393233 | snp | A/G | 0.5 | 0 | intron-variant | Daw1 | Mm_Celera | 1:83177537 | TTCTCAGCATGATAA[A/G]TGACTTTTTAAAAAT | 71227 |
| rs6393698 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Daw1 | Mm_Celera | 1:83177585 | GGTATTTGTTGACTG[C/T]TGCTTCCTGGTTTTA | 71227 |
| rs32998764 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Daw1 | Mm_Celera | 1:83207768 | CCAAATAGTTTTATA[A/G]GTGAGCTCTTATCTG | 71227 |
| rs32998765 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Daw1 | Mm_Celera | 1:83207219 | GGCTCAAAATGGTTC[C/T]CTGACTCAAGCAACC | 71227 |
| rs32998766 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Daw1 | Mm_Celera | 1:83206980 | CAATCGTGGGCTTCC[C/T]GTTGGACAGCAAAGC | 71227 |
| rs32998768 | snp | A/G | 0.32 | 0.24 | intron-variant | Daw1 | Mm_Celera | 1:83206322 | TTGCAGAATTTTTAT[A/G]TCATGTCTCTATCAT | 71227 |
| rs32998770 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Daw1 | Mm_Celera | 1:83205851 | CGAAGTTCTGCAATT[C/T]AGATCTACTAATGTA | 71227 |
| rs32998772 | snp | G/T | 0.32 | 0.24 | intron-variant | Daw1 | GRCm38.p3 | 1:83205565 | TGGTGTTACTGGGTT[G/T]TGAACCATCCTACCT | 71227 |
| rs32999614 | snp | C/T | 0.32 | 0.24 | intron-variant | Daw1 | Mm_Celera | 1:83205451 | TCACTCTCATCCTGT[C/T]TTGTACATAGCTATG | 71227 |
| rs32999616 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Daw1 | GRCm38.p3 | 1:83205439 | TGGTTTCTAAGTTCA[C/T]TCTCATCCTGTCTTG | 71227 |
| rs32999618 | snp | A/C | 0.32 | 0.24 | intron-variant | Daw1 | Mm_Celera | 1:83205336 | TAATTGCTGTCCCCA[A/C]TTCAGAGCTGAGAGA | 71227 |
| rs32999620 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Daw1 | GRCm38.p3 | 1:83205189 | TTCAGAATAATCTCT[C/T]CTTCTTTTGGAGTAT | 71227 |
| rs32999622 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Daw1 | GRCm38.p3 | 1:83205003 | AAAATGTTAGATTGC[A/T]TAGAATATTGGAAGT | 71227 |
| rs32999764 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Daw1 | Mm_Celera | 1:83198692 | CCATACATAATAGTG[C/T]CATGTTCACAATCAT | 71227 |
| rs32999766 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Daw1 | Mm_Celera | 1:83198626 | TGTTTTGCATTGACT[A/G]TGTCACCTCCTTGAT | 71227 |
| rs32999768 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Daw1 | Mm_Celera | 1:83198606 | TTCTTGATAGTCACA[C/T]GTAATGTTTTGCATT | 71227 |
| rs32999770 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Daw1 | Mm_Celera | 1:83198433 | CCCACAGAGTTATAT[C/T]CCATCAGTTTTATTT | 71227 |
| rs32999772 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Daw1 | Mm_Celera | 1:83198349 | ACAGTGTGTCCATGA[C/T]GCATTGTTTTCCTAT | 71227 |
| rs33000204 | snp | C/T | 0.32 | 0.24 | intron-variant | Daw1 | Mm_Celera | 1:83182874 | TTTTATACTGCAGAA[C/T]GTAATTACAGAGAGT | 71227 |
| rs33000206 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Daw1 | Mm_Celera | 1:83182773 | GGATGGTTCTCAAAT[A/G]CGGGCATTCAAGTAT | 71227 |
| rs33000208 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Daw1 | Mm_Celera | 1:83182614 | GCAGCACCATGGCTA[C/T]CTGGGATGGGTTGGT | 71227 |
| rs33000210 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Daw1 | Mm_Celera | 1:83182571 | GGTGCCGGGCTCGTT[G/T]CCTGGCTACAGGAGC | 71227 |
| rs33000212 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Daw1 | GRCm38.p3 | 1:83182562 | GACTATGTGGGTGCC[A/G]GGCTCGTTGCCTGGC | 71227 |
| rs33000404 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Daw1 | Mm_Celera | 1:83204961 | GAAGCAATACAGGAC[A/G]TAATCCTTCATACAT | 71227 |
| rs33000406 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Daw1 | Mm_Celera | 1:83204431 | GACCGACAACTGACC[A/G]CGCACCTTCAATTCC | 71227 |
| rs33000408 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Daw1 | Mm_Celera | 1:83204216 | CTCAGTGAGGCTACA[C/T]TTTCTATGTATATTG | 71227 |
| rs33000409 | snp | A/T | 0.32 | 0.24 | intron-variant | Daw1 | Mm_Celera | 1:83204137 | TTATGCAACAAAATG[A/T]CTGTTTTTTTCCTCC | 71227 |
| rs33000410 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Daw1 | Mm_Celera | 1:83203857 | TGAACTTTGAAAGTA[A/G]TGGGGTGAAACATCC | 71227 |
| rs33000412 | snp | C/T | 0.32 | 0.24 | intron-variant | Daw1 | Mm_Celera | 1:83203433 | TATCTTCTATGACAC[C/T]GTATTAAAATGTATC | 71227 |
| rs33000604 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Daw1 | Mm_Celera | 1:83198276 | CTCTATACCATGCTC[C/T]ATCTGCCCAAGAGCC | 71227 |
| rs33000606 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Daw1 | Mm_Celera | 1:83198259 | CTTGGAAATGTGCCT[A/G]ACTCTATACCATGCT | 71227 |
| rs33000608 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Daw1 | Mm_Celera | 1:83198232 | ATTAAAGCTATGGAG[A/G]AGTTATGTTTCCTTG | 71227 |
| rs33000610 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Daw1 | Mm_Celera | 1:83198206 | TCTGCCGATGGTAAG[A/T]CATTTGACACATTAA | 71227 |
| rs33000612 | snp | C/T | 0.336735 | 0.234472 | synonymous-codon, nc-transcript-variant | Daw1 | GRCm38.p3 | 1:83198196 | CGCAACAGCTTCTGC[C/T]GATGGTAAGTCATTT | 71227 |
| rs33000634 | snp | C/G | 0.32 | 0.24 | intron-variant | Daw1 | Mm_Celera | 1:83176209 | AGGCCTCTGGAAGTG[C/G]AGCTAGAGTTGTCCC | 71227 |
| rs33000635 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Daw1 | Mm_Celera | 1:83176195 | TCCCTGATGGCAGAA[C/G]GCCTCTGGAAGTGCA | 71227 |
| rs33000637 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Daw1 | Mm_Celera | 1:83176182 | GCTGACCTGGTAGTC[C/T]CTGATGGCAGAAGGC | 71227 |
| rs33000639 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Daw1 | Mm_Celera | 1:83169847 | TATATTTTCTTCAAG[G/T]TATCACCCTTTTTGT | 71227 |
| rs33000641 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Daw1 | Mm_Celera | 1:83169617 | CAAGGTGTCTGGAAA[G/T]TGTAAGTTGCTCTTA | 71227 |
| rs33000643 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Daw1 | Mm_Celera | 1:83169567 | CTCAACTCTAACATG[A/G]AAACTATTACACACT | 71227 |
| rs33000854 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Daw1 | GRCm38.p3 | 1:83182509 | TCTACTATTGTGTGA[C/G]AGGCACCCAGAGTGC | 71227 |
| rs33000856 | snp | A/G | 0.32 | 0.24 | intron-variant | Daw1 | Mm_Celera | 1:83181971 | CCATATGTAGTGTGT[A/G]TAAAACAGTGTGCCA | 71227 |
| rs33000858 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Daw1 | Mm_Celera | 1:83181956 | AATTTCCGTAGAAAA[C/T]CATATGTAGTGTGTG | 71227 |
| rs33000860 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Daw1 | GRCm38.p3 | 1:83181890 | AATTAATAGTGCAGT[A/G]TAAAATATAATTGAA | 71227 |
| rs33000862 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Daw1 | Mm_Celera | 1:83181859 | AAGATAAATGAGGCA[A/T]TTTAGGATTAAAATT | 71227 |
| rs33001344 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Daw1 | Mm_Celera | 1:83203398 | CTTGATATCTACTTA[C/T]GATAAAAGTATTATA | 71227 |
| rs33001345 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Daw1 | Mm_Celera | 1:83203151 | GTGCCTGATATTCAG[A/G]AAGTGGGTGTCATGC | 71227 |
| rs33001347 | snp | A/C | 0.32 | 0.24 | intron-variant | Daw1 | Mm_Celera | 1:83203122 | TTATCAGCACACAGA[A/C]ATCTTTACTGTATGT | 71227 |
| rs33001349 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Daw1 | Mm_Celera | 1:83203097 | CTCATATTATATTGT[C/G]TTATATCCTTTATCA | 71227 |
| rs33001351 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Daw1 | Mm_Celera | 1:83202772 | ATAGTTCTATAACTT[C/T]GAACAAAGGTTGTGA | 71227 |
| rs33001353 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Daw1 | Mm_Celera | 1:83202573 | TTTTGAAATGATTTT[A/T]GTTCTTTACCTGCTT | 71227 |
| rs33001445 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Daw1 | Mm_Celera | 1:83169409 | TCTGCTGCTGTTCCC[A/T]TGAGTTTCTATGGGG | 71227 |
| rs33001447 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Daw1 | Mm_Celera | 1:83169369 | CTTTAATTAGGCTGC[G/T]AGTTGAAGCTGTGTC | 71227 |
| rs33001449 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Daw1 | Mm_Celera | 1:83168604 | ACAATTTAAATAAGG[A/T]GTCTGAAGGCACATA | 71227 |
| rs33001451 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Daw1 | Mm_Celera | 1:83168451 | GTGTTTACCAATAAA[A/G]AAGAGTAAAGGAACA | 71227 |
| rs33001453 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Daw1 | Mm_Celera | 1:83168428 | GACAGGGACTCTAAC[A/G]GCCATTAGTGTTTAC | 71227 |
| rs33001494 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon, nc-transcript-variant | Daw1 | Mm_Celera | 1:83198166 | CAGCTGCTTTGATTA[C/T]ACTGGAAAACTTATC | 71227 |
| rs33001496 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon, nc-transcript-variant | Daw1 | Mm_Celera | 1:83198136 | CTTAACAGGCCATGA[C/T]GATGAGATCCTAGAC | 71227 |
| rs33001498 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon, nc-transcript-variant | Daw1 | Mm_Celera | 1:83198112 | TACAAGTGGGAAATA[C/T]GTAGCAACCTTAACA | 71227 |
| rs33001500 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Daw1 | Mm_Celera | 1:83198073 | TGGTGATTTCTATTT[C/T]TCCTAATTTCAGTTG | 71227 |
| rs33001502 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Daw1 | Mm_Celera | 1:83198018 | TATTGAAGATCACTG[C/T]GTGTCTCTCCCACTC | 71227 |
| rs33001584 | snp | A/C/G | 0.391111 | 0.206368 | intron-variant | Daw1 | GRCm38.p3 | 1:83181766 | TTAACCACTCAACAA[A/C/G]TCAGCTATTCAATTA | 71227 |
| rs33001586 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Daw1 | Mm_Celera | 1:83181568 | TCTCCATCTAGTCAA[G/T]TTCCTAGAATGTGAG | 71227 |
| rs33001588 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Daw1 | Mm_Celera | 1:83181229 | CAAGAAGTTGTATTT[C/T]GTGATATGTCAACAT | 71227 |
| rs33001590 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Daw1 | Mm_Celera | 1:83181194 | CCAGCCCTAAAATTA[C/T]TTTCTAGTTAGAGTA | 71227 |
| rs33001592 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Daw1 | Mm_Celera | 1:83180923 | TGACTCTCAGAATCC[C/T]GACTCTCGAGAACTT | 71227 |
| rs33001714 | snp | C/T | 0.142012 | 0.225474 | intron-variant, utr-variant-5-prime | Daw1 | Mm_Celera | 1:83162358 | GTACATTTTAGGATT[C/T]CCCACTGACCTCCAT | 71227 |
| rs33001716 | snp | C/G | 0.459184 | 0.136902 | intron-variant, utr-variant-5-prime | Daw1 | Mm_Celera | 1:83162314 | TTTAGCTCCTTTCCT[C/G]TTTTCACTGTTACCG | 71227 |
| rs33001717 | snp | A/C | 0.277778 | 0.248452 | intron-variant, utr-variant-5-prime | Daw1 | Mm_Celera | 1:83162307 | TTCTGTCTTTAGCTC[A/C]TTTCCTCTTTTCACT | 71227 |
| rs33001718 | snp | C/T | 0.132653 | 0.220748 | intron-variant, utr-variant-5-prime | Daw1 | Mm_Celera | 1:83162082 | CCCTCAGCTGTGGAG[C/T]TCAGGCTAGGAATGT | 71227 |
| rs33001720 | snp | A/G | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Daw1 | Mm_Celera | 1:83161451 | TTCTAAAACTTACAA[A/G]AAGGCCTGTCATGCA | 71227 |
| rs33001722 | snp | C/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Daw1 | Mm_Celera | 1:83161264 | CTTGGCTTTGAGTCT[C/T]ATCTACCGTTTGCCA | 71227 |
| rs33002115 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Daw1 | Mm_Celera | 1:83202490 | TTTGGCTAAGACTTC[A/G]CAGTCCTCTATACTG | 71227 |
| rs33002117 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Daw1 | Mm_Celera | 1:83202472 | TGATCTATCTCTATT[A/T]TTTTTGGCTAAGACT | 71227 |
| rs33002119 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Daw1 | Mm_Celera | 1:83202338 | CAGTAGCTTCCATAT[A/G]TGGAGTAAGCAGAAG | 71227 |
| rs33002121 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Daw1 | Mm_Celera | 1:83201824 | CTTATATTTATATTT[C/T]ATGTTATGGCATGGT | 71227 |
| rs33002123 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Daw1 | Mm_Celera | 1:83201761 | CTGGTGTCACAGAAT[A/G]ATGTCTATCCATATA | 71227 |
| rs33002154 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Daw1 | Mm_Celera | 1:83197758 | TTTTAATTTTCTGTC[C/T]TCATAGTTTTGGATC | 71227 |
| rs33002155 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Daw1 | Mm_Celera | 1:83197689 | TAATTACTGAGAGGC[C/T]GAAACCACCTGCCAC | 71227 |
| rs33002156 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Daw1 | Mm_Celera | 1:83197573 | CATTAATTTTACCCA[A/G]TGTCCCAGTGTTTAT | 71227 |
| rs33002158 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Daw1 | Mm_Celera | 1:83197393 | CAGGTATTCATCAAA[A/G]TAACTAACAGACTTC | 71227 |
| rs33002160 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Daw1 | Mm_Celera | 1:83197384 | ATATTGTGTCAGGTA[G/T]TCATCAAAATAACTA | 71227 |
| rs33002162 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Daw1 | Mm_Celera | 1:83197349 | AGTCAGCCTTGCTTT[C/G]TAAGGTGTCTCTATC | 71227 |
| rs33002184 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Daw1 | Mm_Celera | 1:83168257 | GTTTATAATTACAAG[A/T]AATGGTTAATGTATT | 71227 |
| rs33002186 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Daw1 | Mm_Celera | 1:83168214 | ACATGTCTTTAACTT[A/G]AGAGGTCTACTTCAG | 71227 |
| rs33002187 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Daw1 | Mm_Celera | 1:83168207 | GTCACCTACATGTCT[G/T]TAACTTAAGAGGTCT | 71227 |
| rs33002189 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Daw1 | Mm_Celera | 1:83168196 | CATGATGGCAAGTCA[C/T]CTACATGTCTTTAAC | 71227 |
| rs33002191 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Daw1 | Mm_Celera | 1:83168090 | CCAAGTGTTGCAAGA[C/G]TGTATTGAGACAAAT | 71227 |
| rs33002193 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Daw1 | Mm_Celera | 1:83168060 | CAGATACTTGGGTGA[A/G]CTGTGTAGGTTTTGC | 71227 |
| rs33002284 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Daw1 | Mm_Celera | 1:83180514 | GCTTAGGGACATCAG[A/G]ACCATGGCTGCTACC | 71227 |
| rs33002285 | snp | C/G | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Daw1 | Mm_Celera | 1:83180405 | TCTGATCACAGCGTC[C/G]CGGACAAAGCAAGTC | 71227 |
| rs33002286 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon, intron-variant, nc-transcript-variant | Daw1 | Mm_Celera | 1:83180360 | TACTGATGTCAACAC[C/T]CTAGTAGGAGAGATC | 71227 |
| rs33002288 | snp | C/T | 0.32 | 0.24 | intron-variant | Daw1 | Mm_Celera | 1:83180235 | GTCCTCCTGTCTGTA[C/T]GTGGGCACCTTTACC | 71227 |
| rs33002289 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Daw1 | Mm_Celera | 1:83180153 | AGTCTCCTTGTTGTG[C/T]GTTCTGCCTCTTGAC | 71227 |
| rs33002290 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Daw1 | Mm_Celera | 1:83180012 | ACCCCGGATTCACAG[C/T]GTAGGAAACCCTATG | 71227 |