SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs528820734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23509719 | ACATAATGAGACCCC[A/G]TCTCTTAAAGGAAAA | 23062 |
rs528884442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23491875 | TAACTAAAGAGGTAG[C/T]TGCTGAGGCCCAGAG | 23062 |
rs528898410 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499705 | CTGACCTCGTGATCC[C/G]CCCGCCTCGGCCCCC | 23062 |
rs528998693 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23472254 | GCTGGAGTGCAGTGG[C/T]GCAATCTCAGCTCAC | 23062 |
rs529019145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23492467 | CAGCAATGATGTGTA[A/G]AAAAACAAAACAAAA | 23062 |
rs529020233 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23472482 | GGATTACAGGCATGA[A/G]CCACCACACCCAGCC | 23062 |
rs529035464 | in-del | -/CTGAG | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23502051 | GCATGTGACAGTGGT[-/CTGAG]CTGAGCTGGAGTCCA | 23062 |
rs529127813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23469546 | ATCTCACATTGGCCA[A/G]GTGTCTCATATCCCA | 23062 |
rs529177541 | snp | C/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499213 | GCAGCGGCACAATCT[C/T]GGCTCGCTGCAACCT | 23062 |
rs529322154 | in-del | -/CGACCCC | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23506267 | ATACTATCAATCCCA[-/CGACCCC]CTTATCCCTCCATTG | 23062 |
rs529323514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23475708 | CAGGAGTTCAAGACC[A/G]GCCCGGCCGACATGG | 23062 |
rs529360532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23468264 | CTCACTGCAACCTCC[A/G]CCTCTTGGGTTCAAG | 23062 |
rs529412775 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23504680 | AATCTGCTCCAAGGA[C/G]TAGCTAGGGGCCAGA | 23062 |
rs529466406 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23489308 | GGTGTGATCATGGCT[C/G]GCTGCAGCCTCAAAC | 23062 |
rs529505418 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23507660 | CACAAATTAGCCGGT[G/T]GTGGTGGCGTGTGCC | 23062 |
rs529522820 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463923 | ATTGAGCTACAATCA[C/T]GCCACTGCACTCCAG | 23062 |
rs529630549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23489794 | GGGAAGGCCTGAAGG[C/T]GGGATTAGGGGGAGA | 23062 |
rs529642007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23479696 | AGGCATGTGCTCCGC[A/G]AAGGGAACCAGCTCA | 23062 |
rs529689058 | in-del | -/AA | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23483193 | AAGACTACAGGCTAC[-/AA]AAGTGTATGATTTCT | 23062 |
rs529708883 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23480520 | CACTTTCACAGGAAG[A/G]GGAACAAAGGGCGAG | 23062 |
rs529734741 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | GGA2 | GRCh38.p7 | 16:23472239 | CACTGTGTCACCCAG[C/G]CTGGAGTGCAGTGGC | 23062 |
rs529746831 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23490326 | CAGGGATTAAAAACT[C/T]CTTACCTCACTGATG | 23062 |
rs529770438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23472830 | ACGAGGTCAAGAGAT[C/T]GAGACCATCCTGGCT | 23062 |
rs529812480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501190 | TCTGTACTCTTTTTC[A/G]AGTCATAAAACTACA | 23062 |
rs529848727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23493744 | AGACCCTTTGAGAGG[A/G]GAAAGTGGCTAAAGA | 23062 |
rs529989455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23486638 | TCTACCCCTCAAGCA[C/T]AGGCTCATATGCACT | 23062 |
rs530028409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23471375 | GTTTATTTGAGGGGG[A/G]AAAACTATGTAAGAC | 23062 |
rs530098935 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463484 | TGGGAAGAATTTTCA[C/T]CTTTCATAATTTTGA | 23062 |
rs530137682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23507668 | AGCCGGTTGTGGTGG[C/T]GTGTGCCCGTAATCC | 23062 |
rs530168954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500436 | CTGACATCTATGAGG[C/T]GGTGGCAAGCAGAGG | 23062 |
rs530247137 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23478267 | GATGTTTCTCCAGGG[C/G]GAGAGGCTGTCTTAG | 23062 |
rs530248945 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23508271 | GGGTTTCACCATGTT[G/T]GCCAGGCTGGTCTTA | 23062 |
rs530285619 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | GGA2 | GRCh38.p7 | 16:23470736 | CCTAAGTGACAGAGC[A/G]AGACTCTGTCTCAAA | 23062 |
rs530318911 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511412 | GATCTGCCCGCTTCG[A/C]CCTCCCAAAGTGCTG | 23062 |
rs530417746 | in-del | -/A | 0.0183617 | 0.0940409 | intron-variant | GGA2 | GRCh38.p7 | 16:23474867 | AATAGATTCCCAGGG[-/A]AAAAAAAAAAAAGGT | 23062 |
rs530455577 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23509075 | CTGCCTGAAGTCTCA[C/T]CCTCTCCGCCCAATT | 23062 |
rs530541358 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | GGA2 | GRCh38.p7 | 16:23492986 | ACCTGAGACTGGCTG[-/A]GCTAAGACAGGTGCC | 23062 |
rs530551760 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23497602 | TCTCCTCCCCACCCC[A/C]GCAAAGCTCTCTCCC | 23062 |
rs530555555 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23505307 | GTAGCGCTACCAGAG[A/C]TAGAATTCTAGAGCC | 23062 |
rs530575294 | in-del | -/GA | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464852 | AGGAGGTGGCAGCTT[-/GA]GAGAGGTCTACAACC | 23062 |
rs530624110 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23487785 | CTCATTCTAACAACA[C/G]GGACCTGATGGCCAC | 23062 |
rs530672665 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467515 | CTCCGCACTGAAACA[C/T]CGTGATTAGTCCTGA | 23062 |
rs530734785 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511357 | GTAGAAACGAGGGTT[C/T]ACTATGTTGGCCAGG | 23062 |
rs530902174 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23495604 | TCCTTGCCTAGAGAG[A/C]TTAACCCTAAAACAG | 23062 |
rs531110400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23502399 | TGTTAGGGGAGCTAC[C/T]GAAGTGAAAACTGAA | 23062 |
rs531121104 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465814 | GGCGTGCTGGCTCAC[A/G]CCTGTAGTCCCAGCT | 23062 |
rs531159323 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466394 | ATTATAAACTTGAAT[A/T]CTTCCATCAACAAAT | 23062 |
rs531170062 | snp | C/T | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511668 | CTGCATCACACAGTA[C/T]ACCATCGATGTATTA | 23062 |
rs531344118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23484992 | ACAACCCAAATGCCC[A/G]TCAGCTGATAAATGG | 23062 |
rs531483815 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23485872 | AGACAAAGGGAGGAC[A/G]AAGCAGCACAACGAC | 23062 |
rs531490222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23506295 | CCTCCATTGCAGCAC[C/T]AATGGCCCACCATCC | 23062 |
rs531503490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23506905 | AGGTCCCCCTTTTTG[C/T]TCTGGCTCTGAGCTC | 23062 |
rs531539986 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499801 | TCATTTGTTGAAACC[A/C/G]TAAGACCTTCCTCAC | 23062 |
rs531557671 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23479527 | CCCTACTCACACTCT[A/C]CCTGACTTGCTCAGC | 23062 |
rs531589737 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23483994 | CACCAGGAAGACATT[A/T]AAAAAAAAAAAAGGC | 23062 |
rs531797302 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23469780 | GTCAAGAGATACAGA[A/T]TCTTAAGGCATTGTT | 23062 |
rs531800120 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23490722 | CCTGGGCAACAGAGT[A/G]AGACTCTGTCTCAAA | 23062 |
rs531841615 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | GGA2 | GRCh38.p7 | 16:23479491 | CAGCAGACACGTGTT[C/G]TCCGAGGGTCCAGCT | 23062 |
rs531860964 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23505774 | ACCCAAGCCAACAGG[A/C]GGAAGAACAATAACT | 23062 |
rs531938707 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23486864 | AAGCAGCAGCAACAG[A/C]AGAGTTAACACTAAC | 23062 |
rs532001415 | snp | C/T | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511452 | GGGTGAGCCACCACG[C/T]CCGGCCTATGTGCTT | 23062 |
rs532156682 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23473989 | AGGAGGGCTCTGTGC[C/T]AAAGAGTCCAGGCCC | 23062 |
rs532186875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23487736 | AAGCAGGAGGAAAGC[A/G]GAGAAAGGTGGCCTG | 23062 |
rs532193693 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466510 | TCCTTTACTTCTCGA[C/T]AGAAGACAGTTCCCT | 23062 |
rs532305974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23494580 | CCTACAGCACCCAAG[A/G]TCCTCCTCCTGCCCA | 23062 |
rs532368790 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464984 | AAAAAGAGCAGTCAC[A/G]GAGGTAGGTCACGAA | 23062 |
rs532421056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23481347 | CATTGCACTCCAGCC[A/G]GGGCAGCAAGAGCGA | 23062 |
rs532507376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23508408 | TGTTCTCCATTGCCT[C/T]CTAAAACTACTACCT | 23062 |
rs532583242 | snp | A/G | 4.2163e-05 | 0.00459126 | intron-variant | GGA2 | GRCh38.p7 | 16:23478977 | CAGATGAAGAGTAAT[A/G]CCACACCCATCCTTT | 23062 |
rs532627323 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23464192 | ATTGTTTTCAACACT[A/G]TCTTCATGACCTGTT | 23062 |
rs532673936 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23502004 | AGTCTCAAGCAGGTG[A/C]CAGTGATGTCCACAG | 23062 |
rs532678382 | snp | A/C | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510673 | AAGACGCCCAGTTAA[A/C]TTTGATTTTCAGAAG | 23062 |
rs532678467 | snp | A/G | 3.30207e-05 | 0.00406316 | missense | GGA2 | GRCh38.p7 | 16:23479818 | ACAGTCCCCATCTGC[A/G]CAGGTCCATTGTCCA | 23062 |
rs532799247 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | GGA2 | GRCh38.p7 | 16:23472157 | TCTTTGTAGCCCTGG[C/T]ATCCAAAGATGTTCT | 23062 |
rs532924591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23505424 | GGACACCCATACAAC[A/G]GGGCGTCTAAGGCTT | 23062 |
rs532925157 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499009 | GCAGAGGCAGGAAGA[C/G]AACAGGGGGAGGCAG | 23062 |
rs533026301 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23475441 | GTGATCCGTCCGCCT[C/T]GGCCTCCCAAAGTGC | 23062 |
rs533040392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23468675 | GATGGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 23062 |
rs533049911 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23477534 | GGATCATGAGGTCAA[G/T]AGATCGAGACAATCC | 23062 |
rs533062983 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23481760 | ACTCCAGCCTGAGCA[A/C]CAGAGTGAGACTGTC | 23062 |
rs533081917 | in-del | -/T | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23502931 | ATGTGAGATGTCAGA[-/T]TTAAGTTTTTGTGGA | 23062 |
rs533090412 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23491001 | TAGTTTGAGACCAGC[A/G]TGGGTAACATTGCAA | 23062 |
rs533241804 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23472421 | CAGGTTGGTCTCAAA[C/G]TCCTGACCTCAGGTG | 23062 |
rs533255759 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23512113 | GTAGGGATGGCACCA[C/T]GTTTGAAAGGCGGAA | 23062 |
rs533293591 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23504868 | TATGATTCATTTCAA[A/G]CGTGCTACAGGGCCA | 23062 |
rs533335987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23489244 | ATTCACAATATTTTT[A/G]TTGTTTTTGAGACAG | 23062 |
rs533373240 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23489683 | ATTATTTAAAAATTG[A/T]CTACAGGCCAGTGTG | 23062 |
rs533375096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23482236 | ACAACTGCACTCTAA[C/T]CTGGACGACAGAGCG | 23062 |
rs533445324 | snp | C/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466361 | TCCTAGCACACAGTA[C/G]GTGCTAAGTGGGAAT | 23062 |
rs533523092 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23506692 | CCCAGCTCTCCGTCC[A/G]GGTGGGCCCACTTCG | 23062 |
rs533570757 | in-del | -/TT | 0.288386 | 0.247035 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511319 | CACCACACCCAGCTA[-/TT]TTTTTTTTTTTTGTA | 23062 |
rs533576618 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504095 | TCAAAAAAAAAAAAA[A/T]AAGTACCTACTATGG | 23062 |
rs533594290 | snp | A/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501537 | TTAGTTTTCCTCACA[A/G]AGATAAAGCACAGAA | 23062 |
rs533605109 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23463689 | GGCTTTAAAACAAAC[G/T]GGGGTCAGGACATGG | 23062 |
rs533654637 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23507845 | ATTTAAAAAAAGCTA[G/T]AACTGGGGAGGCTGA | 23062 |
rs533710915 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23492184 | CTTGTTATTCAAGAG[A/T]CACACTCGCAGGGTG | 23062 |
rs533723010 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23496400 | GGGTGTTGGCTTCAC[A/G]CTCGAGTTGGGATGC | 23062 |
rs533934636 | in-del | -/C | 0.00517822 | 0.0506191 | intron-variant | GGA2 | GRCh38.p7 | 16:23507655 | ACACACACAAATTAG[-/C]CGGTTGTGGTGGCGT | 23062 |
rs534017514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23506403 | GCCATGAAGACTGCA[A/G]CCCACATTCCTGATG | 23062 |
rs534054985 | snp | C/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499966 | CTCTGGGCCAGATTG[C/G]TTCCTGGGAACCAGG | 23062 |
rs534059692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499256 | TTCAAGCGATTCTCC[A/G]GCCTCAGCCTCTAGA | 23062 |
rs534103041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23476018 | TTGTTATGAAGGTTG[C/T]TCATGTTGTACCTGT | 23062 |
rs534139625 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23476942 | GAAGTAAAATGAGAA[A/C]AGGGAAGCAGCACAT | 23062 |
rs534280231 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23502839 | AGAAAGTGCTGAGGA[A/T]CAACTGCCCCAGAGT | 23062 |
rs534287419 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23498708 | TGTTTATTATTACGT[A/C]CAGTCTCTGGCTTTT | 23062 |
rs534327605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23491404 | CATAGGTAGCTTGTA[C/T]TTTGACCTTTTTCAT | 23062 |
rs534416754 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23495081 | ACTCTGTCTCAGGAA[A/G]AAAAAAAAAAGAAAA | 23062 |
rs534438901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23495844 | ACCCCTCCCCATACA[C/T]ATGGTGGCCAAGAGC | 23062 |
rs534525841 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23472938 | CTCGGGAGGCTGAGG[C/T]AAGAGAATGGTGTGA | 23062 |
rs534591644 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23509385 | GCGGTCGGCTGTGAC[A/G]ACCCCCAGGTAAACC | 23062 |
rs534610883 | in-del | -/CAGGAGGACTGCTTGAGCC | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23463745 | TTTGGGAGGTCAAGG[-/CAGGAGGACTGCTTGAGCC]CAGGAGACCAGCCTG | 23062 |
rs534627124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23509864 | AGCCAGATAGAGATC[C/T]TTCTCAGCCCCAAAC | 23062 |
rs534723549 | snp | A/G | 0.000123562 | 0.00785912 | intron-variant | GGA2 | GRCh38.p7 | 16:23478600 | CCCACCCAAGCTGCT[A/G]TGGCCCAGACTGGTG | 23062 |
rs534911366 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23493232 | GCTTGGAGAGGAGAG[A/C]GCTTCTTTCACAGGC | 23062 |
rs534946274 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23491056 | AATATTTGGTGTAAG[C/T]GAGACAGCAAGTGAG | 23062 |
rs535090318 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23476146 | CTACTATCCACTCCA[A/T]GATTTTGTTCATTTG | 23062 |
rs535113607 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23483644 | TTCTTTTTGATTGTT[G/T]GTTTTTTTGGTTTTT | 23062 |
rs535164265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23468322 | AGCTGAGACTACAGG[C/T]GCACGCCACCATGCC | 23062 |
rs535209788 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23464241 | CAGATAAGGAAACAT[C/T]TTTGCCCAGTCTTAA | 23062 |
rs535218012 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23477044 | GCAGCCTCGACTTTC[C/T]GGGCTCAAGTGATCC | 23062 |
rs535401744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23483125 | TCAGAAGGCCTCCCA[A/G]TGGTCCTGACTTAGA | 23062 |
rs535485303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23491907 | CACAAGCTCCCAGGC[A/G]CGGTATGAGTGTGAG | 23062 |
rs535599910 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23512194 | GGGTGGTCTAGTGGC[A/T]GTGGGCTGGACAGGA | 23062 |
rs535604773 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23497099 | GGGAGAGCAAGATCC[C/T]GCCTCAAAAACAAAA | 23062 |
rs535735954 | snp | C/T | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465872 | CTTGAACCTGGTAGG[C/T]AGAGATTGCAGTGAG | 23062 |
rs535749513 | snp | G/T | | | missense | GGA2 | GRCh38.p7 | 16:23486124 | ACCGCACTGACCCTC[G/T]TGGACACCTTCTCCG | 23062 |
rs535775609 | snp | A/G | | | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463229 | ATACAAGGAAACTAT[A/G]AGGGAACTGCTACCC | 23062 |
rs535777151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23490286 | CTCAAATCCTGTCTA[C/T]CAAAAGGAAAGCTCT | 23062 |
rs535929584 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511760 | TTATGAAATGAATAC[A/G]TGTTAAATATTTTAT | 23062 |
rs535949799 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23507985 | GGAGTTGAAGAACTG[G/T]GTCCTTGGGCAGCCT | 23062 |
rs535978628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504492 | TGGCTGGACATACTG[A/G]TAACACGGAGAGATG | 23062 |
rs536005830 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | GGA2 | GRCh38.p7 | 16:23484441 | AAACAAAACAAAACT[C/T]CCGCTTCAAAAGATG | 23062 |
rs536030417 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23485436 | GACTGTAAAATGGTG[A/C]AATCACCCTTGAAGA | 23062 |
rs536207992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499326 | ATTTTTTGTATTTTC[A/G]GTAGAGATGGGGTTT | 23062 |
rs536236155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23471896 | CCTAGGCGATGGAGC[A/G]AGGCCCCATCTCTAA | 23062 |
rs536236260 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23463745 | TTTGGGAGGTCAAGG[C/T]AGGAGGACTGCTTGA | 23062 |
rs536241335 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23482685 | ACCTCTCACACCCCA[A/G]TCTCCATGGTCAATT | 23062 |
rs536272536 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464658 | ATGCAACTACTCTGC[A/G]GATACAGACGAAGCA | 23062 |
rs536309374 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465176 | AAAAAAACAGAGACA[C/T]GGTCTCACTATGTAG | 23062 |
rs536367952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23508852 | TCTCTGCCTAAACCA[A/G]CTCCTCCTCACAGGG | 23062 |
rs536383876 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23492780 | ATGCAGAAGTGCAGC[A/T]GCTTGAGGACACATG | 23062 |
rs536465324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23469934 | GACAGGTAAGTCCCA[C/G]AAAAGAACCTGGCAC | 23062 |
rs536501380 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463188 | CTGCTTGGCTGCCTG[A/G]GAATGGTGCCAGCGG | 23062 |
rs536540899 | in-del | -/CCCT | 0.00199481 | 0.0315187 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510558 | CCACCCCAGGCCCCC[-/CCCT]CCTCCACGCGGGACC | 23062 |
rs536596254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23479264 | CTCAGCAGCAGGCAT[A/G]TGCTTCCTGAGGAGA | 23062 |
rs536606503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23495960 | AGCACAGCATTGGGC[A/G]CATGGTATGCCCTTA | 23062 |
rs536677295 | in-del | -/CAAA | 0.0129504 | 0.0794198 | intron-variant | GGA2 | GRCh38.p7 | 16:23470748 | AGCGAGACTCTGTCT[-/CAAA]CAAACAAACAAACAA | 23062 |
rs536765655 | in-del | -/GAGCCC | 0.00159617 | 0.0282053 | cds-indel | GGA2 | GRCh38.p7 | 16:23463759 | GCAGGAGGACTGCTT[-/GAGCCC]AGGAGACCAGCCTGG | 23062 |
rs536782383 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23489380 | GCTGGGACTACAGGT[G/T]GGCACCACCACACCC | 23062 |
rs536785543 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23484396 | GCACTCCAGCCTGGG[A/C/T]GACAGAGCGAGACCT | 23062 |
rs536838504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23474380 | TTTTTTTTTTGGAGA[C/T]GGAGTCTCACTTTGT | 23062 |
rs536893668 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | GGA2 | GRCh38.p7 | 16:23510045 | CAGGTCACGTAGCCA[C/T]TGGGGTGGGGGTCGG | 23062 |
rs536907514 | snp | A/C/G | 0.00199529 | 0.0315338 | intron-variant | GGA2 | GRCh38.p7 | 16:23474634 | TTTTTTTCTTCCCCC[A/C/G]CAAATAGAGACAAGG | 23062 |
rs536937705 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23505790 | GGAAGAACAATAACT[C/G]TTGCAAATCAATGGG | 23062 |
rs536945483 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23488044 | GTCCCTCTAGATACT[C/G]ATGTCCAAGGAATAA | 23062 |
rs536977061 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23477497 | GCCTGTAATCCCAGC[A/G]CTTTGGGAGGCTGAG | 23062 |
rs537194382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23473168 | AGGCTTATAAAGTAA[C/T]AGTAAATAGAGTATA | 23062 |
rs537210227 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23490621 | GTGCCTGTAATCCCA[C/G]CTACTCGAGAAGCTG | 23062 |
rs537335076 | snp | C/G | 0.00597247 | 0.0543191 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510557 | GCCCACCCCAGGCCC[C/G]CCCTCCACGCGGGAC | 23062 |
rs537421810 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23487873 | ATACCACGCAGAAAC[A/G]AGTACGCAGCGTGTA | 23062 |
rs537459571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23481012 | CTACACCTGTACTGT[C/T]CAGAGTAATGGCCAG | 23062 |
rs537598941 | snp | A/C/T | 0.000746182 | 0.0193032 | intron-variant | GGA2 | GRCh38.p7 | 16:23493592 | CTATGAGGACACTGA[A/C/T]GTTTTGATGAAGAGG | 23062 |
rs537603175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501564 | AGAAACTGGAGGCTG[C/T]GTCATGGCCGTGTGA | 23062 |
rs537603496 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23498588 | TTACAAAAAATAAAA[C/G]AAGGAAAATAGTACC | 23062 |
rs537660749 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23486968 | TCCCAATACACCACT[A/G]GTTTTCTTTTCTGTT | 23062 |
rs537740099 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23494171 | TCTCCCTCCTCCAAC[A/C]TGCTGTGAAGGTAAA | 23062 |
rs537772080 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23484022 | GGCCAGGCATGGTGG[A/C]TCATGCCTGTAATCC | 23062 |
rs537778859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23494738 | TAGAGCAGAAAGTGC[A/G]ATCAAACTCTGGGTT | 23062 |
rs537821200 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23477110 | TCATGACCTACCACG[A/C]CTGGCTAATTTTAGT | 23062 |
rs537893394 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23512336 | CCCCGTATGGCCTGC[A/G]TTCCACAGGATGGGG | 23062 |
rs537981880 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23473306 | TCTGGCTGTTAATGG[C/T]ATAGATGATTTTACT | 23062 |
rs538089820 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23509739 | TTAAAGGAAAAAAAA[A/C]ACACACATATATATA | 23062 |
rs538133267 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23491265 | TGAGCCATGACTGCA[C/G]CACTGTGCTCCAGCC | 23062 |
rs538174528 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23491929 | GAGTGTGAGGAGAGA[A/C]TAGAGGCCACACCAT | 23062 |
rs538200162 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23509227 | AAGGCTCTTGAAGAT[C/G]TCGCCCCAATTAGCC | 23062 |
rs538319679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23504992 | TGCCAACCAACCACC[A/G]GGGTCATGACCCTGG | 23062 |
rs538339204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23509810 | AAAAAGTCTGGCCAA[A/G]GTAAACACAAAAGGT | 23062 |
rs538342893 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23484206 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTAACCA | 23062 |
rs538349519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501646 | ATTTCATTGGTATTC[A/G]GTGCACTAATGCCAT | 23062 |
rs538358188 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | GGA2 | GRCh38.p7 | 16:23497832 | CCTCAGTTTCCTCAA[A/C]TATAAAATAAAGAAA | 23062 |
rs538381678 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23482119 | AAAATACAAAATTAG[A/C]CAGGCGTGATGGTGG | 23062 |
rs538428007 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23479333 | CAGCAGCAGGCACTT[G/T]CTCCCAGAGGGAACC | 23062 |
rs538435579 | snp | C/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500534 | AAGCGGGGCAGTGTG[C/T]GGGGCCTGGGGAGCT | 23062 |
rs538586010 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23467853 | GGAAACAGGCACATA[C/T]CCTGGGAACCCTTCG | 23062 |
rs538613904 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23492812 | GACTCACGGCTGGCA[G/T]CTGAAACACAGGAAG | 23062 |
rs538624581 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465276 | AGGCGTGAGCCACTG[C/T]GCACAGCCAATAACT | 23062 |
rs538639115 | in-del | -/A | 0.00478275 | 0.0486673 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510559 | CACCCCAGGCCCCCC[-/A]CTCCACGCGGGACCG | 23062 |
rs538650329 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23485542 | ATAAGAAATGAAAAT[A/C]GATGTTCACACAAAA | 23062 |
rs538743684 | snp | A/G | 1.64874e-05 | 0.00287113 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23493420 | GGCCACCTCGCTGTG[A/G]AACTTCTCCCCACAG | 23062 |
rs538754889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23502529 | GGTCTCAGCAATTGT[C/T]AACAAAAGCCTCTTA | 23062 |
rs538833973 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463218 | GGAGGGAGAGGATAC[A/C]AGGAAACTATGAGGG | 23062 |
rs538837035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23479993 | TAATCAAATGGTAAC[A/G]CCCTCCCTGCCCTTC | 23062 |
rs538955440 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23507317 | TTAATACAATGTATA[A/T]GCCATGAAAAAAACC | 23062 |
rs538981421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500497 | CAGCAGATGGAACAC[A/G]CTGTTGCCCAATGCC | 23062 |
rs538984378 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464813 | ATAACCCCTGACAGA[C/G]TGAAATACGATCTGG | 23062 |
rs538992168 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500010 | GGTTGGCAGGGCAAC[C/G]TCCTTCAGTTGGTGG | 23062 |
rs539015480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23489517 | AGTGCTGGGATCACA[A/G]GCGTGAGCCACCATG | 23062 |
rs539067681 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23490075 | TGACAAGGGATGGCT[A/G]TCTACTGCTACGAGT | 23062 |
rs539139132 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23484375 | CGGAGCTGAGATCAC[A/G]CAATTGCACTCCAGC | 23062 |
rs539164250 | in-del | -/GTGTGTGTGTGTGTGTGTGT | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510929 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTGTGTGTGT]TAGAGACTGGGTTTC | 23062 |
rs539185763 | snp | A/G | 0.00256396 | 0.0357128 | intron-variant | GGA2 | GRCh38.p7 | 16:23483052 | CCCAGGCACCCCATA[A/G]CGCCCCCCTCCAGGG | 23062 |
rs539208665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23470922 | GCAACCTCTGCCTCC[C/T]GGATTCAAACGATTC | 23062 |
rs539209787 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503856 | GGAGGCCAAGGTGGG[C/T]GGATCACCTGAGGTT | 23062 |
rs539319428 | snp | C/T | | | missense | GGA2 | GRCh38.p7 | 16:23488643 | TCAAAGATGGAGCTC[C/T]TGGGCCAGGGAGATG | 23062 |
rs539393399 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23492574 | GCAAGCTCAGAGTCC[-/A]GGGGAGGGCACAGCA | 23062 |
rs539425597 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23473407 | AGTGGCACGATCTCA[C/G]CTCACTGCAACTTCT | 23062 |
rs539761937 | in-del | -/CGCAAGCTTCTCC | 0.0023933 | 0.0345097 | intron-variant | GGA2 | GRCh38.p7 | 16:23508689 | TCTGCTCTTAATATA[-/CGCAAGCTTCTCC]CGCAAGCTCACTGCC | 23062 |
rs539820252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23481580 | GAGTTTGAGACCAGC[C/T]TGGCCAACATGGCAA | 23062 |
rs539835012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23474549 | TTTTTGTAGAGAGAG[A/G]GCTTCGTTATGTTGG | 23062 |
rs539872071 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467155 | GTCCCTGAGAACAGC[A/C]GCCTGGGAGCAACCA | 23062 |
rs539955137 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510574 | CCTCCACGCGGGACC[G/T]GCCGGAACATTTCTT | 23062 |
rs539990823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23494838 | TGTAATCCCAGCACT[C/T]TGGGAGGTCAGGGCA | 23062 |
rs540078912 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23495057 | GCCCTTGCACTCCAG[C/T]CTTGAGACACTCTGT | 23062 |
rs540176403 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23481176 | CTGAGGTCAGGAGTT[C/G]GAGACTATCCTGGTC | 23062 |
rs540176677 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | GGA2 | GRCh38.p7 | 16:23488659 | TGGGCCAGGGAGATG[A/G]TGGGGGTAAGATTTT | 23062 |
rs540215336 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23497980 | CTCCACAGAAATTTT[A/T]AAAAAAAATTAGTCA | 23062 |
rs540280134 | in-del | -/AT | | | intron-variant | GGA2 | GRCh38.p7 | 16:23509743 | GGAAAAAAAAAACAC[-/AT]ACATATATATATATA | 23062 |
rs540280586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23506085 | AAAGCCTTTGATTCT[C/T]TCAACAACCCTAAGA | 23062 |
rs540307260 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23506785 | AGCACCCAATACTCA[G/T]GTGGCAATGGTGGCA | 23062 |
rs540309695 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499016 | CAGGAAGAGAACAGG[A/G]GGAGGCAGGGAGAGA | 23062 |
rs540344332 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499653 | ATCCCGAGTAGGGAC[A/G]GGGTTTCACCATGTT | 23062 |
rs540396403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23483808 | ATGCGCCACCACGCC[C/T]GGCTGATACTGTATT | 23062 |
rs540397785 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | GGA2 | GRCh38.p7 | 16:23476562 | GTAATGTAGCTATTA[A/C]GACTGAGGCATATTT | 23062 |
rs540425890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23468681 | GTTTCACCATGTTGG[C/T]CAGGCTGGTCTCAAA | 23062 |
rs540501348 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23504647 | GCCACAGCAACCGCC[C/G]TAGGTCTGTTTGACA | 23062 |
rs540538141 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23505091 | GAATGCAATCCTTCA[G/T]CAGTCCACGCTGCAG | 23062 |
rs540572272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23489769 | TTCTCCAGAGGCTCA[C/T]GAAAACAGCGGGAAG | 23062 |
rs540628281 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23486587 | TTCCCCAGAGTTCAG[G/T]GCTAGGAGCCACTCT | 23062 |
rs540760984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23483245 | GGCAGGGTGGCTCAC[A/G]TCTGTAATCCCAGCA | 23062 |
rs540876988 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23508198 | CGGCCTCCCAAGTAG[A/C/T]TGGAATTACAGGTGT | 23062 |
rs540881706 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23486613 | ACTCTTTCTCCCAGG[C/T]AACCGTTCCTCTACC | 23062 |
rs540912917 | in-del | -/AATC | 0.00119737 | 0.0244387 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511808 | CCAAGCAGATGTTAT[-/AATC]AATCCAAAAGTGAAG | 23062 |
rs540937265 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23497372 | AACTTCCTCCCGCTG[C/T]GCCAACCCCACTGCT | 23062 |
rs540980559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23494431 | AAAAAGAAACTAACC[C/T]GAGTGGCTGAGCATG | 23062 |
rs540990915 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23493736 | TTTTAAGGAGACCCT[G/T]TGAGAGGAGAAAGTG | 23062 |
rs541032507 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23471257 | ACCTTATATTTAATT[A/G]TACAAAACTGTAGAT | 23062 |
rs541067597 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23481373 | AGCGAAACTCCATCT[C/T]AAGAAAAAAAGAAAT | 23062 |
rs541077438 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23470365 | CCTCCAAACTGACCT[C/T]TCCCCACCATCCAAC | 23062 |
rs541136754 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | GGA2 | GRCh38.p7 | 16:23507638 | CTCTCTCTCTCTCTC[A/T]CACACACACAAATTA | 23062 |
rs541159913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23480512 | AACATATCCACTTTC[A/G]CAGGAAGGGGAACAA | 23062 |
rs541199194 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464840 | CTGGCGACAGCAAGG[A/T]GGTGGCAGCTTGAGA | 23062 |
rs541208449 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463991 | AACAAACCCACTTTT[A/G]TACTCTTGACGCTGG | 23062 |
rs541218152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23492352 | ACCTGTGGAGGTGGT[A/G]GGGCGGGCAGGGGGG | 23062 |
rs541267458 | snp | C/T | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465678 | GGGTGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 23062 |
rs541396429 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23475335 | GCTGGGATTACAGGC[A/T]CCTGCCACCATGTCC | 23062 |
rs541533765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23504689 | CAAGGACTAGCTAGG[C/G]GCCAGACAGGGCACG | 23062 |
rs541618760 | snp | A/G | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510696 | TTCAGAAGAACACGA[A/G]TAATTCTTTTAGCAT | 23062 |
rs541739244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23485632 | CAAGGCCCATCAACA[A/G]GTACATGCTGTGGTA | 23062 |
rs541753148 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | GGA2 | GRCh38.p7 | 16:23474880 | GGAAAAAAAAAAAAA[A/G]GTGGGGAGTGAAATT | 23062 |
rs541756597 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23489560 | CTTCCCTGAATACAT[C/G]AGAGAGCCCAGATCA | 23062 |
rs541907552 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510720 | TTAGCATTTTTATTT[C/T]TTAAGAGACGGGGTC | 23062 |
rs542065058 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465777 | GAAATCCTGTCTCTA[C/G]TAAAAATACAAAAAT | 23062 |
rs542102817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23481955 | AATCTGAACACTGAC[C/T]GAATCTTTGATTATT | 23062 |
rs542282910 | snp | A/G | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504263 | CTCCACAGCCTGGAT[A/G]TGTTTCTAACCACTC | 23062 |
rs542330025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23495587 | TAGGCATGAGCCACC[A/G]ATCCTTGCCTAGAGA | 23062 |
rs542349367 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23488464 | CACCCAAACCTTCTG[C/T]TACCTCACTCCTAAG | 23062 |
rs542409375 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23481277 | ATTCGGGAGGCTGAG[C/G]TGGGAGAATTGCTTA | 23062 |
rs542519096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23510258 | AGCAAGGCCCCGGGA[A/G]GCGGGAAGCGAGGCC | 23062 |
rs542564907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23506876 | CAAAAGGTGTCCTTC[C/T]TCTCTGTGAGGCCAG | 23062 |
rs542575689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23491474 | GCAAACCCTACATCA[C/T]CTTTCCAGGTTTGCA | 23062 |
rs542588712 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | GGA2 | GRCh38.p7 | 16:23507118 | TCATGAAAAACAGCT[A/G]AGGAGGCCACTGGCT | 23062 |
rs542634264 | in-del | -/AG | | | intron-variant | GGA2 | GRCh38.p7 | 16:23507782 | TCCAGCCTGGGCAAC[-/AG]AGCAAGACTCCATCT | 23062 |
rs542692007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499720 | GCCCGCCTCGGCCCC[C/T]CAAAGTGTTAGGATT | 23062 |
rs542727179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23492472 | ATGATGTGTAAAAAA[A/G]CAAAACAAAACAAAA | 23062 |
rs542776950 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23478038 | TCTCTACTAAAAATT[A/T]AAAAAAAAAAATTAG | 23062 |
rs542814709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23469684 | GATAAAGAGGGTTAA[A/G]GACCATGCAACCCTG | 23062 |
rs542853579 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23470363 | ACCCTCCAAACTGAC[A/C]TTTCCCCACCATCCA | 23062 |
rs542860110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23505210 | ATGGGAATGTCCTAC[C/T]CATCACCTGGGAGTA | 23062 |
rs542938024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23498814 | AGTGCCTTACCCATA[C/T]GTACAACATAGAAAC | 23062 |
rs542974761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23488147 | AACACACAGCAGCAA[A/G]TTCTTCCACTGTCCC | 23062 |
rs542988674 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463316 | GCTCAGGGAAGAGAG[C/T]GGGGTTATGTTTCTA | 23062 |
rs542994054 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23477762 | AAAAACAAACAAACA[A/G]ACAAAAACACATGCC | 23062 |
rs543175683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23477351 | GGGTGCAGTTTCCCC[A/G]TACTGTTCTCACGGT | 23062 |
rs543190174 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23481779 | AGTGAGACTGTCTCA[A/T]AAAAAAGGAAAAAGG | 23062 |
rs543297132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23494523 | ACAAACAGGCCACGC[A/G]GGGGCCCTGGAGAGG | 23062 |
rs543324355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23490675 | AGGAGGCGGAGGTTG[C/T]AGTGAACAGAGATCG | 23062 |
rs543333841 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23495379 | ATCCTGTGTTTTTTT[C/T]CCCCCACATGAATTT | 23062 |
rs543335836 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23487659 | TGACACAGGATTGTT[C/T]CTCAGAAGTCACACC | 23062 |
rs543385150 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23472077 | AAATGTCTACATGTG[C/G]CATTTCACTGGTATT | 23062 |
rs543435715 | snp | C/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464822 | GACAGACTGAAATAC[C/G]ATCTGGCGACAGCAA | 23062 |
rs543502047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23481327 | GCAGCGAGCTGAGAT[C/T]GCACCATTGCACTCC | 23062 |
rs543541050 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23473862 | TCTTAAATCAAAAAT[A/C]AATAAAGAAATGTGC | 23062 |
rs543556689 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465621 | GGTACCTCTTCAAGA[A/C]TACGCAACAGTAACA | 23062 |
rs543569905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501246 | TGTACATCGAACGAC[C/T]TTTAACTAATGGTAG | 23062 |
rs543613230 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23485780 | CATCATTCCATTTAT[A/G]CAAGAGTCTGGGAGT | 23062 |
rs543648562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501926 | CCTTCTTGAACAACT[C/T]TTGGGGAGAAGGAGT | 23062 |
rs543737610 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23485437 | ACTGTAAAATGGTGC[A/G]ATCACCCTTGAAGAT | 23062 |
rs543759550 | snp | A/G | 1.81641e-05 | 0.00301359 | intron-variant | GGA2 | GRCh38.p7 | 16:23478953 | CCTAACAGTAACTCC[A/G]CCTGCTTCCAGATGA | 23062 |
rs543779471 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | GGA2 | GRCh38.p7 | 16:23468523 | CTGTTGCCCAGGCTG[G/T]AGTGCAGTAGTGCGA | 23062 |
rs543977575 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23508038 | CTCCTCCACCTGAGG[C/G]AGCTACTTTCTCTTA | 23062 |
rs544051122 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23505059 | AGACTGTGAGGAAGT[A/G]GTCACCCCGAGGAGC | 23062 |
rs544175738 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23483192 | AAAAGACTACAGGCT[A/T]CAAGTGTATGATTTC | 23062 |
rs544207668 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23469267 | AGCATCAACAGCCAG[G/T]GCACATCTTGGGTTG | 23062 |
rs544235677 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504601 | GCTCCAAAAAATGAC[C/T]CCCAGGGGGCCAGCA | 23062 |
rs544372363 | snp | C/T | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23463764 | AGGACTGCTTGAGCC[C/T]AGGAGACCAGCCTGG | 23062 |
rs544407378 | snp | C/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23502391 | CTTGGGATTGTTAGG[C/G]GAGCTACCGAAGTGA | 23062 |
rs544453635 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23474690 | CTCCTGGCCTCAAGT[C/G]ATCCTCCCACCTCAG | 23062 |
rs544520902 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23510423 | CCATCGCTCCAGCCC[A/C]GACGCTGCGGCCGCG | 23062 |
rs544539146 | in-del | -/TTTTCA | | | cds-indel, downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23464181 | GGTTGTCATTTATTG[-/TTTTCA]ACACTATCTTCATGA | 23062 |
rs544570998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23496212 | GGAGGCTGAGGCAGG[A/G]GAATCGCTTGAACTT | 23062 |
rs544576141 | snp | C/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467276 | AGGCAGGGACAGTGT[C/G/T]GCTCGCTGACATGCA | 23062 |
rs544614963 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23498253 | ACACTGCACTCCAGC[A/C]TGGGTGACAAGGTGA | 23062 |
rs544633696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23493037 | CAAGGCAGGAGGTGA[C/T]AGGAAACTTTCACGC | 23062 |
rs544746659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23489625 | AAAAAACAACCTCCA[A/G]GGATTGACAAAAGGC | 23062 |
rs544943263 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23505457 | CATTTAAAAGAACAA[A/G]GCGGCTACATCTGCA | 23062 |
rs544971249 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23487507 | AGTTGCCCTGGACCA[C/T]GTGCTTTATGACACA | 23062 |
rs544993042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500193 | GGGTGCGGGCTGCTA[A/G]TGGGGAGCAGCCCCA | 23062 |
rs545045672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23467878 | CCTTCGATAATTCTG[C/T]AGTCCTGAAATCCTG | 23062 |
rs545075699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23478147 | AAGGCTGTAGTGAGC[C/T]GAGATTGTGCCACTG | 23062 |
rs545085567 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23497985 | CAGAAATTTTTAAAA[A/C]AAATTAGTCAGAAGG | 23062 |
rs545164487 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23471165 | TTAATTCTACCCAGA[A/C]ATAAGCACTTACTTC | 23062 |
rs545199953 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463334 | GGTTATGTTTCTAAG[C/T]AATTCATATTGATAA | 23062 |
rs545209047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23470446 | CGATCATTATTAAAA[C/T]AATGCATGAACACTA | 23062 |
rs545289483 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23491575 | TGTCTATGGTCCTAC[A/G]TAAGAAGTACAGCTT | 23062 |
rs545323014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23492287 | AACCTTGTGATCAGA[A/G]GGCTGAAACTTTCAG | 23062 |
rs545357423 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23481835 | CCACTAAGAGAGACA[A/G]AAGAAATATAAACCA | 23062 |
rs545378314 | in-del | -/TTTTT | 0.0154538 | 0.0865337 | intron-variant | GGA2 | GRCh38.p7 | 16:23468110 | ACTGACTTTCTTTTC[-/TTTTT]CTCTTCTCCTTCCTT | 23062 |
rs545410249 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23471725 | GGCAATACAGTGAGA[G/T]CTGCCTCCCACCCTC | 23062 |
rs545494477 | snp | A/G | 0.00517822 | 0.0506191 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510954 | GTGTGTGTGTTAGAG[A/G]CTGGGTTTCACCATG | 23062 |
rs545524127 | snp | A/G | 7.35537e-05 | 0.00606395 | intron-variant | GGA2 | GRCh38.p7 | 16:23478744 | AGTATGGGTGAGGAA[A/G]AGGCTTTGGACCTCC | 23062 |
rs545618671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23475259 | CAATCGAACAGTCTC[A/G]GCTCACTGCAACCTC | 23062 |
rs545675315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499468 | TTTCTTTAAGAAAGA[A/G]AAAACCTCTCTGAGG | 23062 |
rs545686426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23488347 | GGGGTAAGGCAGGAT[C/T]ACAAACAGATCCTAC | 23062 |
rs545728236 | in-del | -/T | 0.447421 | 0.153379 | intron-variant | GGA2 | GRCh38.p7 | 16:23470826 | AAATGAAATAAATGC[-/T]TTTTTTTTTTTTTTT | 23062 |
rs545749459 | in-del | -/AGTG | | | intron-variant | GGA2 | GRCh38.p7 | 16:23492226 | TCACTAATGACTTAC[-/AGTG]AGTGCCTAGAGAGCT | 23062 |
rs545767916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23496049 | TCATGCCTGTAATCC[C/T]GGCATTTTGGGAGGC | 23062 |
rs545785697 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23474839 | AAACTGGAGTGGAAA[A/C]AGCTGGGAGTCTAAT | 23062 |
rs545787230 | snp | A/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500992 | ATAACAGAACAGTCA[A/G]CCAGCCTGATCTTTG | 23062 |
rs545922894 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467349 | CGCATTTCCCACACT[A/G]CCGATATCCCAAGCC | 23062 |
rs545933094 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23495497 | ACAGAGTCTCTCACT[C/T]TGTCACCCAGGCAGG | 23062 |
rs545956070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23502176 | CAACAATGGTGGGAA[A/G]AGAGAGTGGCATCGG | 23062 |
rs545976154 | snp | A/G | | | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463490 | GAATTTTCACCTTTC[A/G]TAATTTTGAATCATG | 23062 |
rs546083283 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | GGA2 | GRCh38.p7 | 16:23472158 | CTTTGTAGCCCTGGC[A/T]TCCAAAGATGTTCTT | 23062 |
rs546089306 | in-del | -/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23489115 | AACCTGAGTTCCTTC[-/T]TTTAAGAGCCCAACA | 23062 |
rs546155208 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465668 | CACAGAGGCCGGGTG[C/T]GGTGGCTCACGCCTG | 23062 |
rs546346979 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23492692 | GTGCTTTCCTGTGTA[C/T]GTGAATCATTCTAGG | 23062 |
rs546382537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23479602 | ACACCCATCCTGACT[C/T]CCTCAGCAGCAAGCA | 23062 |
rs546382760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23487431 | CTGTGAACATCCTAC[A/G]GTGCACAGGACAGTC | 23062 |
rs546419612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23480292 | AGGGACCGCATTTCA[A/G]CCAGTGCTCCAGGTG | 23062 |
rs546516508 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23472750 | AAAAAAAAGACTGAA[A/T]AGGGCCGGGCGCAGT | 23062 |
rs546756131 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23468241 | GGAGTGCAGTGGTGC[A/G]ATCTTGGCTCACTGC | 23062 |
rs546793196 | snp | C/T | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465423 | CTCCTCCTACCCCTA[C/T]CCTGTCCAACACCTA | 23062 |
rs546927960 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23505429 | CCCATACAACGGGGC[A/G]TCTAAGGCTTTTCAT | 23062 |
rs546968945 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | GGA2 | GRCh38.p7 | 16:23482325 | AGACTAGGGAATGGG[C/T]GTGTACAAAGAGAGG | 23062 |
rs546994042 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23489261 | TGTTTTTGAGACAGA[G/T]TCTTGCTCTGTCTCC | 23062 |
rs547002975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23486933 | GGTCCAAGGACACTA[C/T]GATGCAGGCACTCTG | 23062 |
rs547107680 | snp | C/T | 6.63317e-05 | 0.0057586 | missense | GGA2 | GRCh38.p7 | 16:23475032 | CCTGGTGGCACTTCC[C/T]TGGGGACACTTTTCT | 23062 |
rs547207591 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464349 | AGGACTTTATTGTGG[C/G]TGTGGTGAAGCAGGC | 23062 |
rs547220371 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23508976 | CTGCTGACTACGCCT[-/C]GCTCATTGCTTCTCC | 23062 |
rs547357398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23485197 | AAATCCAGAGAGACA[A/G]AAAGTGGATTAGTGG | 23062 |
rs547395278 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23482009 | TCGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 23062 |
rs547396301 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23477111 | CATGACCTACCACGC[A/C]TGGCTAATTTTAGTA | 23062 |
rs547497138 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499866 | ATGAATGAAAGGTAG[A/G]GGTGGGGCCGCTGGC | 23062 |
rs547512322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23479686 | CCTCAGCAGCAGGCA[C/T]GTGCTCCGCGAAGGG | 23062 |
rs547543722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23484178 | TTTGGGAGGCTGAGA[C/T]GGGTGGATCACCTGA | 23062 |
rs547543783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23476994 | TCTCACTCTGCTGCC[C/T]AGGCTGGAATGCAGT | 23062 |
rs547547194 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23472216 | TTTTTTTTTTTTAGA[A/C]ACAGTCTCACTGTGT | 23062 |
rs547617293 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23507951 | GGTGACACAGTGAGA[-/CT]CTGTTTCAAAAAAAG | 23062 |
rs547679250 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23477638 | TGTAATCCCAGCTAC[C/T]CAGGAGGCTGAGGCA | 23062 |
rs547775173 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463408 | AAAACACAGAACAGT[A/C]TACTATATTTTCTTG | 23062 |
rs547784244 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23507677 | TGGTGGCGTGTGCCC[A/C/G]TAATCCCAGCTACTT | 23062 |
rs547814351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503728 | GAAAACGGATTTTCC[C/T]ATGGGGGGAAAAAAG | 23062 |
rs547908617 | snp | C/G | 0.00478085 | 0.0486577 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511015 | AGAGACTGGGTTTCA[C/G]CGTGTGTGTGTGTGT | 23062 |
rs547953824 | snp | C/G/T | 5.02907e-05 | 0.0050143 | missense | GGA2 | GRCh38.p7 | 16:23483001 | CACACCTCTCATACA[C/G/T]GACCTGAAAGAGCAG | 23062 |
rs548037220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23481431 | TGGGGGATGCCACGA[A/G]CAAAACTGAGACCGA | 23062 |
rs548060981 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23506497 | ATCCCACTCAACCCT[G/T]GGGAAACATGGCAGT | 23062 |
rs548113663 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466740 | TTGGCCGATTCATCA[C/T]GACTGACATGGTGTG | 23062 |
rs548163458 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23510476 | CTGTAGCGTCCTGGC[G/T]CTCTCCTCTGCTGAC | 23062 |
rs548267871 | in-del | -/G | 0.00597247 | 0.0543191 | intron-variant | GGA2 | GRCh38.p7 | 16:23509976 | TCGGGGTGGGAATGA[-/G]GATTAAGCAGGACTA | 23062 |
rs548295438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23480916 | GGTTGTGTCATCGGA[C/T]CCTATCAGGCCTAGT | 23062 |
rs548578758 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23497755 | CAGATATTTTATCTG[A/C/T]CCCTTCTCCGATAGG | 23062 |
rs548607852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23494161 | CTGGCCCAGATCTCC[C/T]TCCTCCAACCTGCTG | 23062 |
rs548646493 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23494712 | GGCTGTGATAAATAC[C/T]TAGGAAATGCTAGAG | 23062 |
rs548651745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23487857 | AGTTGACAGGCAGAG[C/T]ATACCACGCAGAAAC | 23062 |
rs548668597 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23493051 | ATAGGAAACTTTCAC[A/G]CCACCCCTGGGATCT | 23062 |
rs548688876 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23509257 | CGTGCAGCCCCTTTC[C/T]CGGATTCCTGAGCTT | 23062 |
rs548733680 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465107 | TCCCCAGAGGAAAAG[A/C]AGCTCCTTCAGGGTG | 23062 |
rs548774967 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23483335 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 23062 |
rs548789963 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23484211 | TCAGGAGTTCGAGAC[C/T]AGCCTAACCAACATA | 23062 |
rs548868879 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501504 | CCTTGGCAAATGACC[G/T]TGACCTGTATTTTCT | 23062 |
rs548938978 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23505464 | AAGAACAAGGCGGCT[A/T]CATCTGCAGTCATGT | 23062 |
rs548947742 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23481428 | TCATGGGGGATGCCA[C/T]GAGCAAAACTGAGAC | 23062 |
rs548975017 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23472925 | TGTGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAA | 23062 |
rs549045758 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23491905 | GACACAAGCTCCCAG[A/G]CGCGGTATGAGTGTG | 23062 |
rs549209786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23497557 | AGAGAACACAAGGGC[A/G]AGGGAAGGATCAGTG | 23062 |
rs549269000 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23498558 | CATAGTGAGGCCCCA[G/T]CTCTACAAATATGTT | 23062 |
rs549307519 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23491194 | CGCCTGTAGTCCCAG[A/C]TGCTTGGGAGACTGA | 23062 |
rs549358887 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23475713 | GTTCAAGACCAGCCC[A/G]GCCGACATGGTGAAA | 23062 |
rs549385470 | snp | A/C | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511711 | TTCTGTTAAAAGATA[A/C]TTTTCCCAAAAAAGT | 23062 |
rs549394326 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23489875 | AGAGAAAAAACAGGG[A/G]AGAAAAAACAAAAAC | 23062 |
rs549425646 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23512237 | TTTGTAAAGAGCATC[A/G]GTTTATATAGTATTT | 23062 |
rs549496819 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23468274 | CCTCCGCCTCTTGGG[G/T]TCAAGCAATTCTCCT | 23062 |
rs549518336 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23493807 | TCCAGTGCCCAAGAC[C/T]AGCCGGATGTCACCC | 23062 |
rs549533668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23468829 | TACCCACAAAGTTAC[C/T]TCCCCTTACAGTTCA | 23062 |
rs549599243 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23489309 | GTGTGATCATGGCTC[A/G]CTGCAGCCTCAAACT | 23062 |
rs549610488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23472850 | CCATCCTGGCTAACA[C/T]GGTGAAACCCTGTCT | 23062 |
rs549638339 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23482352 | GAGGTACAGATGAAG[A/T]AAGATTAAAAAAATC | 23062 |
rs549649016 | snp | A/C/T | 8.23627e-05 | 0.0064168 | missense | GGA2 | GRCh38.p7 | 16:23486735 | AAATTCTTGATTAAC[A/C/T]GGTTTGCAGCCTGAA | 23062 |
rs549757976 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23472249 | CCCAGGCTGGAGTGC[A/C]GTGGCGCAATCTCAG | 23062 |
rs549804620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499943 | GGGAACAGGGCATGT[A/G]GAGGGGACTCTGGGC | 23062 |
rs549841773 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500459 | AGCAGAGGTGCAGGC[C/T]AAGGCAGAGAGGAGT | 23062 |
rs549850925 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | GGA2 | GRCh38.p7 | 16:23509767 | ATATATACGCACACA[C/T]ACACACACGTGTGTG | 23062 |
rs549902261 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465177 | AAAAAACAGAGACAC[A/G]GTCTCACTATGTAGC | 23062 |
rs550050827 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23476415 | CTATGAAAATGTTGT[C/T]ACATTCACACCTTAG | 23062 |
rs550059580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23470858 | TTTTTGGACAGACTT[C/T]CGCTTTTGTTGCCCA | 23062 |
rs550156376 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23479551 | GCTCAGCAGCAGACA[C/T]GTGCTTCCCAAGGGG | 23062 |
rs550282005 | in-del | -/TG | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23482482 | TTCTTTTTTAGTAAC[-/TG]TGGACAATTCTCCAC | 23062 |
rs550308735 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23478302 | CCATTCTCTGGCCCT[C/T]GTCCCATGAGAAGGA | 23062 |
rs550337098 | snp | A/G | 3.30284e-05 | 0.00406363 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23479829 | CTGCGCAGGTCCATT[A/G]TCCACCTCCAAGTCA | 23062 |
rs550362454 | snp | A/G | 0.000120603 | 0.00776447 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23467599 | GAAAAGTTAGGCTGC[A/G]CCCAAGACAGCCAGG | 23062 |
rs550497811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23468081 | TATACCCCTAACACC[C/T]AACCAAACCAGAGAC | 23062 |
rs550514504 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23468476 | CCACTGCACCTGGCC[A/G]ACTTTATTTTTTTTT | 23062 |
rs550645522 | snp | A/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499588 | GTATCATGAGGACTC[A/T]ATCAAGATTTATTGG | 23062 |
rs550670207 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23498097 | CCAGCCTGGGCAACA[C/G/T]GGTGAAATCCCGTCT | 23062 |
rs550824160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23482072 | AGAAGTTTGAAACCA[A/G]CCTGGCCAAAATGGT | 23062 |
rs550898604 | snp | A/C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23512079 | TTGAAGCTGTTGTGC[A/C/T]GTACCCCTATTAACT | 23062 |
rs550973412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503351 | TGTAGAGTCTACTCT[C/T]TGGTGAATACACAAA | 23062 |
rs551310046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23487878 | ACGCAGAAACGAGTA[C/T]GCAGCGTGTAGCCTT | 23062 |
rs551325012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499202 | CGGGCTGGTGTGCAG[C/T]GGCACAATCTCGGCT | 23062 |
rs551340458 | snp | C/T | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23502977 | GGCAGAATCCTAAGA[C/T]GCCCCATGATCTCTG | 23062 |
rs551351212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23485012 | CTGATAAATGGAGAA[A/G]CAAACTGTGGCATAG | 23062 |
rs551379295 | in-del | -/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499870 | ATGAAAGGTAGGGGT[-/G]GGGCCGCTGGCAGGG | 23062 |
rs551429073 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23472423 | GGTTGGTCTCAAACT[C/T]CTGACCTCAGGTGCT | 23062 |
rs551451850 | snp | C/T | 0 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23469108 | CCAAGAGGAAATGGC[C/T]CTCTTAAACGTGGTA | 23062 |
rs551489484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23485884 | GACAAAGCAGCACAA[C/T]GACATTTGGGGAGGT | 23062 |
rs551493440 | snp | A/C | 6.61704e-05 | 0.00575159 | missense | GGA2 | GRCh38.p7 | 16:23470071 | GGTCAAGAGCAGCAC[A/C]TGTACCTCTGGGTGC | 23062 |
rs551514632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23490736 | TGAGACTCTGTCTCA[A/G]AAGAAAAAAAAAAAA | 23062 |
rs551592157 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23507000 | TTCCCCAATGGAACA[A/T]CAACATGAAGAGGGG | 23062 |
rs551597386 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | GGA2 | GRCh38.p7 | 16:23473610 | TGGGATTACAGGCAT[A/G]AGCCACTGCGTCTGG | 23062 |
rs551629833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499834 | TGTAGAAACCTGAAA[A/G]CTCCCAGCAGCCAGC | 23062 |
rs551712342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23492577 | AGCTCAGAGTCCAGG[A/G]GAGGGCACAGCAGCT | 23062 |
rs551792682 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23509814 | AGTCTGGCCAAAGTA[A/C]ACACAAAAGGTAAAA | 23062 |
rs551829604 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23510467 | CTTCAGCCGCTGTAG[A/C]GTCCTGGCGCTCTCC | 23062 |
rs551889173 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466514 | TTACTTCTCGACAGA[A/G]GACAGTTCCCTTTAG | 23062 |
rs551895256 | snp | A/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464971 | TAAGAGACAGAGGAA[A/G]AAGAGCAGTCACGGA | 23062 |
rs551908484 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23487737 | AGCAGGAGGAAAGCG[A/G]AGAAAGGTGGCCTGG | 23062 |
rs552039091 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | GGA2 | GRCh38.p7 | 16:23475861 | CTAGAGCCTGGGAGG[C/T]GGAGGTTGTGGTGAG | 23062 |
rs552117279 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465936 | ACAGAGTGAGATATG[G/T]CCTCAAAAAACAAAA | 23062 |
rs552346242 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23496039 | GCACAGTGGCTCATG[C/T]CTGTAATCCCGGCAT | 23062 |
rs552380604 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23493022 | GACAGGTACAGAGGA[A/C]AAGGCAGGAGGTGAT | 23062 |
rs552473307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23472906 | GGGCGTGGTTGTGGG[C/T]ACCTGTGTCCCAGCT | 23062 |
rs552581874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501386 | CCCAAGGACATTGCA[A/G]TTGAGAACATGAGCA | 23062 |
rs552595263 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23482525 | TGTACCTTCCATTTC[C/G]CATCGGCCTGGCCCT | 23062 |
rs552634477 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23483115 | GTCTGGGGCTTCAGA[A/C]GGCCTCCCAATGGTC | 23062 |
rs552671622 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23476118 | CAGGCAGATGATACA[C/T]AAATTATACCAGCTA | 23062 |
rs552764877 | in-del | -/GCGCAGGGGAAA | 0.00636936 | 0.0560724 | intron-variant | GGA2 | GRCh38.p7 | 16:23510014 | TGAGCACAGTGCCTG[-/GCGCAGGGGAAA]GCGCAGGGGAAAGCG | 23062 |
rs552943105 | snp | A/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23478774 | CAAGGCCATGATCCC[A/T]CCGGGACAGTGCAGG | 23062 |
rs552966597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23496926 | TGGCACCACTGTACT[C/T]AGCCTGGGCAACAGA | 23062 |
rs553003366 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23489518 | GTGCTGGGATCACAG[C/G]CGTGAGCCACCATGC | 23062 |
rs553050190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23474555 | TAGAGAGAGGGCTTC[A/G]TTATGTTGGCCAGGC | 23062 |
rs553058665 | in-del | -/TCTG | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23468168 | TCTCTCTTTCATCTA[-/TCTG]TCTGTCTGTCTATCT | 23062 |
rs553185013 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467213 | AGTGGATGAATGGAA[C/T]GAACGATACATGAAA | 23062 |
rs553201796 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511611 | TCCTGGAACACTTCT[A/G]AACTAACATGTCCTG | 23062 |
rs553202097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503865 | GGTGGGCGGATCACC[C/T]GAGGTTGGGAGTTCA | 23062 |
rs553393416 | in-del | -/GTGT | 0.00557542 | 0.0525036 | intron-variant | GGA2 | GRCh38.p7 | 16:23491097 | AGAGAGAGGAAGAGA[-/GTGT]GTGTGTTTGTGTGTG | 23062 |
rs553463286 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510610 | AGATCCCTCCACCCA[C/G]CGCTGGTCTTCTAAG | 23062 |
rs553540185 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23482337 | GGGTGTGTACAAAGA[C/G]AGGTACAGATGAAGT | 23062 |
rs553649882 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23487897 | GCGTGTAGCCTTCCA[A/C]CACTCCATGAACTAG | 23062 |
rs553686640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23481184 | AGGAGTTCGAGACTA[C/T]CCTGGTCAAAATGGT | 23062 |
rs553762303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23471071 | GCCTCAAACTCCCGA[C/T]CTCAGGTGATCCGCC | 23062 |
rs553782048 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23498712 | TATTATTACGTACAG[A/T]CTCTGGCTTTTACTG | 23062 |
rs553822918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499271 | GGCCTCAGCCTCTAG[A/G]GTAGCTAGGATCACA | 23062 |
rs553896794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500782 | TCGGATTTAGGAGCC[C/T]GCAAGGGCCATGACC | 23062 |
rs553944087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23491426 | CTTTTTCATGCTGTG[A/G]TTTCCTATGATTTCC | 23062 |
rs553986802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23483830 | TACTGTATTTTTAGT[A/G]GAGATGGGGTTTCTC | 23062 |
rs554001869 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463907 | AGGAATTCAAGGCTG[C/T]ATTGAGCTACAATCA | 23062 |
rs554029863 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23468359 | ATTTTTGTATTTTTA[A/G]TAGAGATGGGGTTTC | 23062 |
rs554099148 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | GGA2 | GRCh38.p7 | 16:23492278 | AAGAGATCAACCTTG[-/A]TGATCAGAGGGCTGA | 23062 |
rs554127818 | snp | C/G | 0.000399281 | 0.0141238 | missense | GGA2 | GRCh38.p7 | 16:23478447 | GAACACCACCGCCTG[C/G]CAGCGTGCTGGAGGA | 23062 |
rs554129865 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | GGA2 | GRCh38.p7 | 16:23470345 | TCTAGCTGGACTCCT[A/G]TGACCCTCCAAACTG | 23062 |
rs554139207 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23502854 | TCAACTGCCCCAGAG[C/T]CTACAAGGGAAACAC | 23062 |
rs554252259 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23492192 | TCAAGAGACACACTC[A/G]CAGGGTGCACCTGAG | 23062 |
rs554375768 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23488774 | TTCAGTCAGAATCCA[C/G]TATAAAGTCTGGAAA | 23062 |
rs554420008 | snp | A/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23476924 | TCCTACGACTTAGGA[A/T]AAGAAGTAAAATGAG | 23062 |
rs554442149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23469185 | GATAAAAGGATCTAA[A/G]AGGCCTTTCCTTCCA | 23062 |
rs554455219 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23487619 | TGGGACGGATGGCAG[A/G]AAAAGTGGGGATAAT | 23062 |
rs554456910 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23474043 | TCCTGCTCTGCATAC[C/T]GGTGTAGAGACGGTA | 23062 |
rs554563792 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465977 | CAGAATACAAGCAAG[A/G]AAGTACTTTTAGATT | 23062 |
rs554621874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23488027 | GCCACCTTCTTCTTC[C/T]TGTCCCTCTAGATAC | 23062 |
rs554660676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23481282 | GGAGGCTGAGGTGGG[A/G]GAATTGCTTAAACCC | 23062 |
rs554666444 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | GGA2 | GRCh38.p7 | 16:23472577 | GCTGGACATAGTGGC[A/G]CATGCCTGTAGTCCC | 23062 |
rs554709625 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465490 | AGCAAGAATGTTCAG[G/T]TACACATGTGTGAGT | 23062 |
rs554714666 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23487045 | GGAGTGCAGTGGCGC[A/T]ATCTCGACTCACTGC | 23062 |
rs554950190 | in-del | -/AAAC | 0.0023933 | 0.0345097 | intron-variant | GGA2 | GRCh38.p7 | 16:23477749 | GAGACTCCATCTCAA[-/AAAC]AAACAAACAAACAAA | 23062 |
rs555033616 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23468453 | AGTGCTGGGATTACA[G/T]GCGTGAGCCACTGCA | 23062 |
rs555133952 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23485315 | TCTATAACTAGGTAG[G/T]TGTGATGGTTGCTTT | 23062 |
rs555197825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500057 | GAGGAGCTCCCTCTG[C/T]GCTCTCTTCTCCGCA | 23062 |
rs555197871 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23507966 | CTCTGTTTCAAAAAA[A/C]GCTGGAGTTGAAGAA | 23062 |
rs555213773 | snp | A/G | 2.49909e-05 | 0.00353481 | intron-variant | GGA2 | GRCh38.p7 | 16:23493521 | CAGGCTCCCCTCCAG[A/G]CTGGTAATCACTTGC | 23062 |
rs555254692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23486377 | ATGACCTCTGCCTTT[A/G]TGCCACCAGCCTCAA | 23062 |
rs555390293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23483130 | AGGCCTCCCAATGGT[C/T]CTGACTTAGAGACTG | 23062 |
rs555402569 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | GGA2 | GRCh38.p7 | 16:23485616 | AAAGCTGGAAACAAC[A/G]CAAGGCCCATCAACA | 23062 |
rs555426402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23477055 | TTTCCGGGCTCAAGT[A/G]ATCCTTCTACCTCAG | 23062 |
rs555578959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23489580 | AGCCCAGATCACAGG[A/G]CAACAACCAAGTAAC | 23062 |
rs555704934 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23498074 | TGCCTGAACTCAGGA[A/G]TTGGAGGCCAGCCTG | 23062 |
rs555758806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23467770 | GGGTCAATGTTAAGT[C/T]AAGTGAGTGTTTCAA | 23062 |
rs555930364 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23507420 | ATAACTTGAGGTCAG[A/G]AGTTTGAGACCAGCC | 23062 |
rs555990505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501604 | CTTGCATCAACATGC[C/T]GCTGCTATAAAGGGC | 23062 |
rs556019052 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464727 | AAGAGCATGTAGGTG[A/G]AAAGGGGCAGGACTC | 23062 |
rs556150964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23507989 | TTGAAGAACTGTGTC[C/T]TTGGGCAGCCTCAGT | 23062 |
rs556159436 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464694 | CAGGGACCCAATAAG[G/T]CTCAGGTGCTTTCAA | 23062 |
rs556181031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23492238 | TACAGTGAGTGCCTA[A/G]AGAGCTTCAAGGGCT | 23062 |
rs556259929 | snp | A/G | | | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463382 | TATCTATGGTGTTAC[A/G]TGAAAAGAACAAAAC | 23062 |
rs556294016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23493601 | CACTGAAGTTTTGAT[A/G]AAGAGGACGTTTTCA | 23062 |
rs556296387 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23490149 | GTGAAGACCTACAGC[C/T]GAGAGAACAGATACT | 23062 |
rs556395095 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23478068 | GCTGGGCATGGTGGC[A/G]CGTGCCTGTAATCCC | 23062 |
rs556408203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23498934 | TCACTACAAGGTCAA[A/G]GTTGACACCTCAAAA | 23062 |
rs556438174 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463201 | TGGGAATGGTGCCAG[C/T]GGGAGGGAGAGGATA | 23062 |
rs556449716 | snp | C/T | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503899 | CCAGCCTGACCAACA[C/T]GGAGAAACCCCGTCT | 23062 |
rs556485632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23471137 | TGAGCCACTGCACCC[A/G]GCCAATGCATTCTTA | 23062 |
rs556502233 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23471476 | TGACATAAACAAAAC[A/G]TGTGGAACAGATCTA | 23062 |
rs556633600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23485447 | GGTGCAATCACCCTT[A/G]AAGATAGCTTAGCCA | 23062 |
rs556782752 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23506534 | TGACATTTTTGGCTG[C/T]TATGACTGGGAGGAA | 23062 |
rs556798256 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23482359 | AGATGAAGTAAGATT[A/T]AAAAAATCAGCTATG | 23062 |
rs556837689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23495963 | ACAGCATTGGGCACA[C/T]GGTATGCCCTTACTG | 23062 |
rs556877086 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23492043 | CTGGGTCAGAGCCTG[C/T]TCTACACCACTGGGG | 23062 |
rs556907862 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23498282 | GAGACTCTGTCTCCA[A/C]AAAAAAAAAAAGCCA | 23062 |
rs556941361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503812 | TGGGGCCGGGTGTAG[C/T]GGCTCATGCCTGTAA | 23062 |
rs556998181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23481780 | GTGAGACTGTCTCAA[A/G]AAAAAGGAAAAAGGA | 23062 |
rs557025757 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465639 | CGCAACAGTAACAGA[A/G]CCTATAAAAGCTACA | 23062 |
rs557037074 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23474770 | ACCTCTTACTTTCTG[A/C]CCTCATGCAAAATCT | 23062 |
rs557061306 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463309 | CATATGAGCTCAGGG[A/C]AGAGAGCGGGGTTAT | 23062 |
rs557096269 | snp | A/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23493689 | CAGGAAATAGCTTAG[A/T]GAGGTATGTCAAACC | 23062 |
rs557107064 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23510050 | CACGTAGCCATTGGG[G/T]TGGGGGTCGGGGTCC | 23062 |
rs557147923 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23502979 | CAGAATCCTAAGACG[C/T]CCCATGATCTCTGCT | 23062 |
rs557165625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23473256 | GTATATGATAAGACA[A/G]GAAAATCTATCAAGA | 23062 |
rs557220335 | snp | C/G | 0.00080032 | 0.019988 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510559 | CCACCCCAGGCCCCC[C/G]CTCCACGCGGGACCG | 23062 |
rs557274697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23472665 | GTAAGCTGAGATGGC[A/G]CCACTGCACTCCAGC | 23062 |
rs557384584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23491950 | GCCACACCATCTGGC[A/G]CCCAGCCCCGGAGCC | 23062 |
rs557423138 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23469310 | TTCTCACTAGCTCTG[G/T]GACCTTGAGTAAAAT | 23062 |
rs557459641 | snp | C/G | 0.000802246 | 0.020012 | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463245 | AGGGAACTGCTACCC[C/G]AGAGTTTTAACATGC | 23062 |
rs557691250 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23477788 | ATGCCTTTTGCCTTC[C/T]GCCATGACTGGGAGG | 23062 |
rs557775176 | snp | A/G | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504036 | CGGTGAGCCAAGATC[A/G]TGCCATTGCACTCCA | 23062 |
rs557785254 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23477155 | TGGGGTTTTGCCATA[C/T]CTCCCAGGCTGGTCT | 23062 |
rs557785919 | snp | C/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23497488 | TCTAGATAGGGAGGG[C/T]CAACGGACAGGTAAT | 23062 |
rs557812188 | snp | A/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501053 | ATATTACAACATAAA[A/G]CACAGATACGCAAAT | 23062 |
rs557893318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23505018 | CCTGGCACCAGCAGC[C/T]GCCTGTGCTAGCAAG | 23062 |
rs557919122 | snp | A/G | | | missense, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23494337 | TCCTTCTCTTGCGGA[A/G]ACTGGATCTTGTGGG | 23062 |
rs558023271 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | GGA2 | GRCh38.p7 | 16:23491325 | AAAAAAAAAAAAAAA[A/C]AAAACCAAAAGGTTA | 23062 |
rs558063893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23483733 | CTCACCGCAACCTCC[A/G]CCTCCTGGGTTCAAA | 23062 |
rs558100995 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23484336 | GGCAGGAGAATCGCT[C/T]GAACCCGGGAGGCAG | 23062 |
rs558119322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23469249 | AACCGGCATCTGAGA[C/T]GCAGCATCAACAGCC | 23062 |
rs558188247 | snp | C/T | | | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463510 | TTTGAATCATGTCAA[C/T]GTCTTTATCTTAAAA | 23062 |
rs558207039 | snp | C/T | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464667 | CTCTGCGGATACAGA[C/T]GAAGCAGGAATCAGG | 23062 |
rs558235087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23498647 | AGGGGAAGGGTCTAA[A/G]ATGCTTAGTACAGCA | 23062 |
rs558342853 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23502669 | GAGCAGCGGTTCTCA[C/T]GGGAGCAGCTTCTGC | 23062 |
rs558481864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23467868 | TCCTGGGAACCCTTC[A/G]ATAATTCTGCAGTCC | 23062 |
rs558557371 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501656 | TATTCGGTGCACTAA[C/T]GCCATCTTAAAGAGA | 23062 |
rs558594250 | snp | C/T | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23494329 | AAAGAGCTTCCTTCT[C/T]TTGCGGAGACTGGAT | 23062 |
rs558609217 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465286 | CACTGTGCACAGCCA[A/G]TAACTACTTGTTAAG | 23062 |
rs558643105 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | GGA2 | GRCh38.p7 | 16:23479344 | ACTTGCTCCCAGAGG[A/G]AACCAGCTCACTCCC | 23062 |
rs558672710 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23485562 | TTCACACAAAATCCC[A/G]TACAAAATTGTTTAC | 23062 |
rs558674303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23471979 | TTAAGAGACTGAAAA[C/T]ACCAGTGGGGTATGG | 23062 |
rs558721389 | snp | C/T | 1.68596e-05 | 0.00290336 | intron-variant | GGA2 | GRCh38.p7 | 16:23493477 | CACAGACACAGGACC[C/T]CCAGGAGAAGGTGGA | 23062 |
rs558807463 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464830 | GAAATACGATCTGGC[A/G]ACAGCAAGGAGGTGG | 23062 |
rs558846420 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23488254 | CTTTCCCCCAGGAAG[A/G]CTGTGCACAAAAGGG | 23062 |
rs558921461 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499517 | CCTTAACCAAGGCCA[A/G]GCAGCAATACAATCC | 23062 |
rs558957545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23492318 | CCCCATCCCCTGACC[A/G]GTGCCCCCACATCCC | 23062 |
rs558968874 | snp | C/T | 3.33367e-05 | 0.00408255 | intron-variant | GGA2 | GRCh38.p7 | 16:23474854 | AAGCTGGGAGTCTAA[C/T]AGATTCCCAGGGAAA | 23062 |
rs559066096 | snp | C/G | 0.00478085 | 0.0486577 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511013 | TTAGAGACTGGGTTT[C/G]ACCGTGTGTGTGTGT | 23062 |
rs559167664 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467385 | CTACCACCCTCTCCC[C/T]GAACACACACACACA | 23062 |
rs559176722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500022 | AACCTCCTTCAGTTG[A/G]TGGGAAGCAGTGGAA | 23062 |
rs559194327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23506748 | CGCTTCCCCACCTTC[C/T]TCAAGTCCCCTGTTC | 23062 |
rs559195614 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23481408 | GAAACAGAACATGAG[A/C]AGCATCATGGGGGAT | 23062 |
rs559228770 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23481901 | AATTTTTTTTTTTTA[A/C]GTTAGCAAGAGATGA | 23062 |
rs559232879 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23474093 | CCTTCCATTTCCTTC[C/T]CTTTTAACAGAGATA | 23062 |
rs559420340 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23467953 | TCCTTTCAGAGGACT[A/C]CAGAGGATTAGGGAG | 23062 |
rs559477891 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466000 | TTTAGATTAAAATTC[A/G]TCTTATGTGAATTAT | 23062 |
rs559536075 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | GGA2 | GRCh38.p7 | 16:23477451 | CTGCTGCCACATAAG[A/T]CACGCCTTTTGGCTG | 23062 |
rs559572692 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23489006 | CAGTTTATCCAGCTA[C/T]ATAACCTCCCAGGGA | 23062 |
rs559766962 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23509617 | CATTGGTAAAACGGA[G/T]ATAATAATAACCCCT | 23062 |
rs559777862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23472761 | TGAATAGGGCCGGGC[A/G]CAGTGGCTCACGCCT | 23062 |
rs559807495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23510084 | GCTGCTGCTAAGTTG[A/G]GGGGTGGGCGGAGGG | 23062 |
rs559816092 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465670 | CAGAGGCCGGGTGCG[A/G]TGGCTCACGCCTGTA | 23062 |
rs559845995 | in-del | -/GAG | | | intron-variant | GGA2 | GRCh38.p7 | 16:23486166 | TCCTTTTGGGAAAAA[-/GAG]GAGGATGGGAGTGAG | 23062 |
rs559934641 | snp | A/G | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511069 | AGACTGGGTTTCACC[A/G]TGTTGCCCGGGTGGT | 23062 |
rs559943409 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23478614 | TGTGGCCCAGACTGG[G/T]GACATCTCTTGGGGC | 23062 |
rs559976041 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23475564 | GAATAACAGAAGTAA[C/T]TTACCTCCTAGGGCT | 23062 |
rs559979798 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465019 | GTCAACAGGACCCCC[A/G]AAGAGTTCAAGATAC | 23062 |
rs559980285 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23507649 | TCTCTCACACACACA[A/G]ATTAGCCGGTTGTGG | 23062 |
rs560034542 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23480390 | GTATGCAAGCATTTA[A/T]GAGAATTCAAACGCA | 23062 |
rs560113136 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23505460 | TTAAAAGAACAAGGC[A/G]GCTACATCTGCAGTC | 23062 |
rs560134017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23508511 | TCTCCTTCCTCATTC[C/T]CCTCCATCTTTAAGG | 23062 |
rs560145146 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | GGA2 | GRCh38.p7 | 16:23475122 | ATTTCCTGGAATCTG[G/T]GTTAGGCTTATTAAA | 23062 |
rs560183177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23506105 | CAACCCTAAGAAGAG[A/G]TTTTATTACTCTCTT | 23062 |
rs560210010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23506787 | CACCCAATACTCAGG[C/T]GGCAATGGTGGCACT | 23062 |
rs560295694 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511933 | GTCCCTCCAGTGAGC[A/G]GAATTTACCTATTTA | 23062 |
rs560381351 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23469419 | TAGAGACTGCAGGTC[A/T]TATTTTTGTCTGTCT | 23062 |
rs560437575 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23477284 | CTTGAATTGTAGCAC[A/C]CACAATTCCCACATG | 23062 |
rs560506279 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23482854 | GTTCCTGGCACAGCA[C/G]TGTGACAGGAGGGAC | 23062 |
rs560544803 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23483259 | CGTCTGTAATCCCAG[A/C]ACTTTAGGAGACCAA | 23062 |
rs560566599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23490550 | GACCAGCCTGAGCAA[C/T]GTGGTGAAACCCCAT | 23062 |
rs560580373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23476605 | ATGAAATGCATCACA[A/G]ATATAATATGAAAAG | 23062 |
rs560582752 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23497445 | TTTCCTGACTGCAGT[A/C]ACATTTATGTCACGT | 23062 |
rs560613038 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23497937 | CTAGGAGGTTGAGAC[C/T]AGCCTGAGCAACATA | 23062 |
rs560740537 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500334 | GCCGAGCTGCCTCAC[A/G]GGGAACATGCTGAGC | 23062 |
rs560761881 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23487595 | CACAGAGAAGTCACT[C/T]AATCTTTGTGGGACG | 23062 |
rs560798519 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23480519 | CCACTTTCACAGGAA[G/T]GGGAACAAAGGGCGA | 23062 |
rs560817200 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23493742 | GGAGACCCTTTGAGA[A/G]GAGAAAGTGGCTAAA | 23062 |
rs560851830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23494434 | AAGAAACTAACCCGA[A/G]TGGCTGAGCATGCTC | 23062 |
rs560919580 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23508229 | GCGCCACCACACATG[A/G]CTATTTTTTGTATTT | 23062 |
rs560977885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23479693 | AGCAGGCATGTGCTC[C/T]GCGAAGGGAACCAGC | 23062 |
rs560979399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23472817 | AGGTGGGCAGATCAC[A/G]AGGTCAAGAGATCGA | 23062 |
rs560983063 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23482821 | AAGCTCCACGGAACC[A/G]AAAGTCCACTCTGTC | 23062 |
rs560997224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23471268 | AATTGTACAAAACTG[C/T]AGATACCAAATCACC | 23062 |
rs561196209 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23505589 | GATTCTGGTAACGGC[C/T]TCCTGATACTCCTCT | 23062 |
rs561214585 | in-del | -/ACTT | 0.00199481 | 0.0315187 | intron-variant | GGA2 | GRCh38.p7 | 16:23471172 | TACCCAGAAATAAGC[-/ACTT]ACTTCCTTCTGGTCT | 23062 |
rs561219522 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23478236 | AAGACAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 23062 |
rs561239261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23486627 | GCAACCGTTCCTCTA[C/T]CCCTCAAGCATAGGC | 23062 |
rs561249114 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464843 | GCGACAGCAAGGAGG[C/T]GGCAGCTTGAGAGAG | 23062 |
rs561256315 | snp | C/T | 0.000333067 | 0.0129005 | missense | GGA2 | GRCh38.p7 | 16:23478900 | TGCCTGTAACAGGAG[C/T]ATCACTGATTCCTGT | 23062 |
rs561258350 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23470670 | TGAGAGGCTGAGGCA[C/T]GAAAATCACTTGAAC | 23062 |
rs561297380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23468017 | GACAATCCATCTGAT[C/T]TTCCTTCAGTGAGCC | 23062 |
rs561369035 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23507889 | CTTGAGCCCAGGAGA[C/G]GGGTAAGCTGCAGTG | 23062 |
rs561396654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23485660 | GTACATCCAGGTGAC[A/G]GGACAGTACCCGGCA | 23062 |
rs561462196 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23509741 | AAAGGAAAAAAAAAA[A/C]ACACATATATATATA | 23062 |
rs561563987 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23484911 | ATAAAAACTTGGACA[A/T]AGTTCAAAGTCATTA | 23062 |
rs561580452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23504728 | GAAATTCAAAGGATG[C/T]CTTCTCTGTTTTGGG | 23062 |
rs561625259 | snp | A/G | 3.50496e-05 | 0.00418612 | intron-variant | GGA2 | GRCh38.p7 | 16:23478689 | ACCTCCAGGAAGCAG[A/G]AGCCTGGTGCAACCT | 23062 |
rs561627584 | snp | C/G/T | 0.112268 | 0.208642 | intron-variant | GGA2 | GRCh38.p7 | 16:23474882 | AAAAAAAAAAAAAGG[C/G/T]GGGGAGTGAAATTGT | 23062 |
rs561660236 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467510 | TGGCACTCCGCACTG[A/G]AACACCGTGATTAGT | 23062 |
rs561662255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23475350 | ACCTGCCACCATGTC[C/T]GACTAATTTTTGTAT | 23062 |
rs561839917 | in-del | -/T | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511503 | TTTTCCTGGAACACT[-/T]TTTTTTTTTTTTCAG | 23062 |
rs561851244 | in-del | -/GAGGCA | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23496204 | GCTACTTGGGAGGCT[-/GAGGCA]GGAGAATCGCTTGAA | 23062 |
rs561859254 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23468369 | TTTTAGTAGAGATGG[A/G]GTTTCACCATGTTGG | 23062 |
rs561940766 | in-del | -/CAGGAGGACTGCT | 0.00159617 | 0.0282053 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23463745 | TTTGGGAGGTCAAGG[-/CAGGAGGACTGCT]TGAGCCCAGGAGACC | 23062 |
rs561967826 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463873 | TCCAGAGGCTGAAGC[C/T]GGAGGATCGCCTGAA | 23062 |
rs561993143 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | GGA2 | GRCh38.p7 | 16:23482625 | TTTCTCTGGCCCCTG[C/T]GATTGGTCAGCTTTT | 23062 |
rs562055031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503241 | CTATAGCCCTTTATA[C/T]GTAATTGAATATTTT | 23062 |
rs562093277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503950 | GCCAGGTATGGTGCT[A/G]CATGCCTGCAGTCCC | 23062 |
rs562095169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23495590 | GCATGAGCCACCGAT[C/T]CTTGCCTAGAGAGCT | 23062 |
rs562132139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23496118 | CTAGCCTGACCAACA[C/T]GATGAAACCCCATCT | 23062 |
rs562317348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23473619 | AGGCATGAGCCACTG[C/T]GTCTGGCCTATTCTA | 23062 |
rs562356039 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466376 | GGTGCTAAGTGGGAA[C/T]TGATTATAAACTTGA | 23062 |
rs562369403 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500162 | ACAAGGCAGCTCAGG[C/G]GAGGCAGCTGAGGTG | 23062 |
rs562372126 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23505348 | GAGTGCTGTTTTTAA[C/T]AGCGCAAGGCTAGCA | 23062 |
rs562455686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499758 | TGAGCCACTGTGCCC[A/G]GCTCAGTTTTCTTTT | 23062 |
rs562555156 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23506288 | CCTTATCCCTCCATT[A/G]CAGCACCAATGGCCC | 23062 |
rs562694480 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23475433 | GACCTCAGGTGATCC[A/G]TCCGCCTCGGCCTCC | 23062 |
rs562731508 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23497564 | ACAAGGGCGAGGGAA[C/G]GATCAGTGATTGATT | 23062 |
rs562760618 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463317 | CTCAGGGAAGAGAGC[A/G]GGGTTATGTTTCTAA | 23062 |
rs562771517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23498046 | GCACTTTGGGAGGCC[A/G]AGGAGGGTGGATTGC | 23062 |
rs562782073 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | GGA2 | GRCh38.p7 | 16:23476717 | AAAGCAAAAAAGGAA[C/T]GTTCAACCTTGTTTT | 23062 |
rs562810747 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23490716 | CTCCAGCCTGGGCAA[C/T]AGAGTGAGACTCTGT | 23062 |
rs562848148 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23491522 | AAGTAGATAAAAGAT[A/T]TATTGCGTAAAAAAA | 23062 |
rs562940385 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23483945 | AGCCACTGCGCCCGG[C/G]TGGGCTGTGGTTTCT | 23062 |
rs562975444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23477415 | GGGAAACCCTTTTTC[A/G]TTTGGCTCTCATTCT | 23062 |
rs562986049 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23469763 | TGCCAAAGAAAAGCA[C/G]AGTCAAGAGATACAG | 23062 |
rs563040710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23483387 | TAATCCCAGCTACTC[A/G]GGAGGCTTTCTCTTA | 23062 |
rs563087496 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23505256 | AAGAAACAGATTTAC[G/T]GAGCACCCAACTTTT | 23062 |
rs563133530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23493870 | ACCCCTCCTCTCGTC[C/T]ATACTGTGGCTTTCA | 23062 |
rs563166094 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23495561 | CTTGGTCTCCCAAAC[C/T]GTTGGGATTATAGGC | 23062 |
rs563170343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23494547 | GGAGAGGGCCACCTC[A/G]CACCCACCCTGGTTG | 23062 |
rs563180097 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23481328 | CAGCGAGCTGAGATC[A/G]CACCATTGCACTCCA | 23062 |
rs563208856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23487675 | CTCAGAAGTCACACC[A/G]TACCTCCTTCCTAGC | 23062 |
rs563247470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23488233 | CGGGCTATCCTTCTG[C/T]ACCTTCTTTCCCCCA | 23062 |
rs563264269 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23487621 | GGACGGATGGCAGGA[A/C]AAGTGGGGATAATGA | 23062 |
rs563339197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23472871 | AACCCTGTCTCTACT[A/G]AAAATACAAAAAAGT | 23062 |
rs563547440 | in-del | -/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503730 | AACGGATTTTCCTAT[-/G]GGGGGGAAAAAAGAT | 23062 |
rs563582388 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | GGA2 | GRCh38.p7 | 16:23509517 | GGTGAGCAAGGACCC[C/T]GTGTTATGCATCTCA | 23062 |
rs563618354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23471479 | CATAAACAAAACGTG[C/T]GGAACAGATCTAAAT | 23062 |
rs563694124 | snp | A/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23476097 | TGATCACAAAGGGAC[A/T]TGAGCCAGGCAGATG | 23062 |
rs563714444 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23508346 | GCTGCGATTACAGGC[A/G]TGAACAGCCTTTTTT | 23062 |
rs563949369 | snp | A/C | 1.81628e-05 | 0.00301348 | intron-variant | GGA2 | GRCh38.p7 | 16:23478954 | CTAACAGTAACTCCA[A/C]CTGCTTCCAGATGAA | 23062 |
rs564135808 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23498581 | AATATGTTTACAAAA[A/C]ATAAAACAAGGAAAA | 23062 |
rs564172765 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464996 | CACGGAGGTAGGTCA[C/T]GAAATGGGTCAACAG | 23062 |
rs564172934 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23496415 | ACTCGAGTTGGGATG[C/T]CCCCACCTGGCCTGT | 23062 |
rs564320926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23496218 | TGAGGCAGGAGAATC[A/G]CTTGAACTTGGGAGG | 23062 |
rs564364774 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510796 | ACTGCAGCCTCCACC[C/T]CCTAGGCTCAAGCGA | 23062 |
rs564385463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23476459 | TCAGGGATCTATACT[A/G]TAAGGCACTCCCCCA | 23062 |
rs564396329 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23497103 | GAGCAAGATCCTGCC[-/T]CAAAAACAAAAAAAA | 23062 |
rs564419890 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23512096 | TACCCCTATTAACTT[A/C]AGTAGGGATGGCACC | 23062 |
rs564424421 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | GGA2 | GRCh38.p7 | 16:23468672 | AGAGATGGGGTTTCA[A/C]CATGTTGGCCAGGCT | 23062 |
rs564440885 | in-del | -/GACAGGCTGT | 0.00279162 | 0.0372561 | intron-variant | GGA2 | GRCh38.p7 | 16:23483616 | CTCGAACCTGGCACA[-/GACAGGCTGT]GGTTTCTTTTTGATT | 23062 |
rs564531842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23497367 | CAGAAAACTTCCTCC[C/T]GCTGCGCCAACCCCA | 23062 |
rs564537392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23489652 | AGGCAATACCAATAG[C/T]AACAACTAAGCTAGA | 23062 |
rs564543535 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23482172 | GGGAGGCTGAGGAAG[A/G]AGAATGGCTTGAACC | 23062 |
rs564574442 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23482725 | TTTCAGGCTTTAGAC[A/C]TGCTGCTGATTTCTT | 23062 |
rs564764287 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23493673 | GCCTGAGGTTTATGC[A/C]CAGGAAATAGCTTAG | 23062 |
rs564798718 | in-del | -/TTC | 0.00557542 | 0.0525036 | intron-variant | GGA2 | GRCh38.p7 | 16:23480355 | ACTAAGGAAGATCAT[-/TTC]TTTTGTCTCTAGCTC | 23062 |
rs564884376 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23492804 | ACACATGAGACTCAC[A/G]GCTGGCAGCTGAAAC | 23062 |
rs564886092 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463851 | ATGCACCTGTAGTCC[C/T]AGCTACTCCAGAGGC | 23062 |
rs564944068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23486519 | GAGAAGTACGGCAGC[A/G]GGATTTCTGGTTCCA | 23062 |
rs564953656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499842 | CCTGAAAGCTCCCAG[C/T]AGCCAGCAATGAATG | 23062 |
rs565178138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23469891 | TTATCTTCAGTTAGT[C/T]TGAGTGAAGATTCTT | 23062 |
rs565198418 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23479564 | CACGTGCTTCCCAAG[C/G]GGACCAGCTCACTCC | 23062 |
rs565209188 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23484075 | AGGTGGATCACCTCA[A/G]GCCAGGGTTCAAGAC | 23062 |
rs565245922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23484762 | CAATACATTGCTGCT[A/G]GGAATGTAAAATGGC | 23062 |
rs565317120 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23509854 | TTGACGCGGTAGCCA[A/G]ATAGAGATCTTTCTC | 23062 |
rs565326037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23478148 | AGGCTGTAGTGAGCC[A/G]AGATTGTGCCACTGC | 23062 |
rs565353876 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23502828 | GCTTCCAAAATAGAA[A/T]GTGCTGAGGATCAAC | 23062 |
rs565362533 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23470505 | TGGGGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 23062 |
rs565379520 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23508379 | TAATTTTTGCAACTC[C/T]AGTCTAAGCCTTCTG | 23062 |
rs565397813 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463337 | TATGTTTCTAAGTAA[C/T]TCATATTGATAATGG | 23062 |
rs565448466 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | GGA2 | GRCh38.p7 | 16:23477512 | ACTTTGGGAGGCTGA[A/G]GCAGACGGATCATGA | 23062 |
rs565537553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23480005 | AACGCCCTCCCTGCC[C/T]TTCCAAGAACCTTCC | 23062 |
rs565717649 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466579 | TTCCACTTACTCAAC[A/G]CTCCACAAAGTACAC | 23062 |
rs565722113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23495009 | AGAACCACTTGAACC[C/T]GGGAGGTGGAGGTTG | 23062 |
rs565760030 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23486274 | CACCAGGATGTTAAG[C/T]GCATGGGAGAACTCA | 23062 |
rs565774783 | snp | A/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23482673 | GATCTTTCTTCTACC[A/T]CTCACACCCCAATCT | 23062 |
rs565797091 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23486949 | GATGCAGGCACTCTG[A/C]CTATCCCAATACACC | 23062 |
rs565845243 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465956 | AAAAAACAAAAAAAA[A/G]CCACACAGAATACAA | 23062 |
rs565910178 | snp | C/G | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23512317 | ACCCCAAAGGGCCTT[C/G]ATCCCCCGTATGGCC | 23062 |
rs565919369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501429 | GTTTTTTGGAGCTAC[C/T]TGAGTTTAATATTCA | 23062 |
rs566211466 | in-del | -/TC | 0.0283406 | 0.115616 | intron-variant | GGA2 | GRCh38.p7 | 16:23507621 | AAGAATGAAACTCCA[-/TC]TCTCTCTCTCTCTCT | 23062 |
rs566350634 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23477137 | TAGTATTTTTTGTAG[A/C]GATGGGGTTTTGCCA | 23062 |
rs566410108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500523 | ATGCCAGCCCCAAGC[A/G]GGGCAGTGTGCGGGG | 23062 |
rs566491539 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | GGA2 | GRCh38.p7 | 16:23491089 | AGAGACAGAGAGAGA[A/G]GAAGAGAGTGTGTGT | 23062 |
rs566563362 | snp | A/G | | | missense | GGA2 | GRCh38.p7 | 16:23470016 | GCACAGCCACTTGAA[A/G]CATGATATCCCAGAC | 23062 |
rs566650729 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504443 | TATCTACTGAATGAA[C/G]GATTCCTCTTTTGCT | 23062 |
rs566690992 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23504871 | GATTCATTTCAAGCG[C/T]GCTACAGGGCCAGAG | 23062 |
rs566728108 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23505459 | TTTAAAAGAACAAGG[C/T]GGCTACATCTGCAGT | 23062 |
rs566870938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23482339 | GTGTGTACAAAGAGA[A/G]GTACAGATGAAGTAA | 23062 |
rs566894928 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511726 | ATTTTCCCAAAAAAG[C/T]ATGTCATGATTATCA | 23062 |
rs566966991 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23468246 | GCAGTGGTGCGATCT[C/T]GGCTCACTGCAACCT | 23062 |
rs567205315 | in-del | -/A/AA | 0.0175775 | 0.0920858 | intron-variant | GGA2 | GRCh38.p7 | 16:23474867 | ATAGATTCCCAGGGA[-/A/AA]AAAAAAAAAAAAGGT | 23062 |
rs567301788 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23506472 | CGGGGAGATGGGTAG[C/G]AGTGATCCCATCCCA | 23062 |
rs567308444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23471857 | GAGGCTGCAGTGAGC[C/T]ATGACTGTGCCACCG | 23062 |
rs567331871 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464491 | ATGCTCAGATTTGCT[A/G]GAGAACTCTGGTAGT | 23062 |
rs567339406 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499313 | ACATGACTGGCTAAT[A/T]TTTTGTATTTTCAGT | 23062 |
rs567345079 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | GGA2 | GRCh38.p7 | 16:23472229 | GACACAGTCTCACTG[C/T]GTCACCCAGGCTGGA | 23062 |
rs567378068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499875 | AGGTAGGGGTGGGGC[C/T]GCTGGCAGGGCGGGG | 23062 |
rs567378573 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23493301 | CTGAGGAGGGAGCCA[C/G]GAGTTTGACAGTGGG | 23062 |
rs567394309 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23473052 | AAAAAAAAAAAAGAC[C/T]GAATAAACAGATTAC | 23062 |
rs567397535 | in-del | -/CAAA/CAAACAAA | 0.487666 | 0.233792 | intron-variant | GGA2 | GRCh38.p7 | 16:23470751 | AGACTCTGTCTCAAA[-/CAAA/CAAACAAA]CAAACAAACAAACAA | 23062 |
rs567413126 | snp | G/T | 1.6477e-05 | 0.00287024 | missense | GGA2 | GRCh38.p7 | 16:23486116 | CTTCCTCCACCGCAC[G/T]GACCCTCTTGGACAC | 23062 |
rs567480601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23485409 | GCTAGAACTTGCATA[C/T]GCTGCTGTTAGGACT | 23062 |
rs567531166 | snp | C/G | 1.66983e-05 | 0.00288944 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23478460 | TGGCAGCGTGCTGGA[C/G]GAGGGATTCCTCTTT | 23062 |
rs567536329 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23485708 | GCTACACACAGCAAC[A/G]TGAATGGATCTCGAG | 23062 |
rs567555403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23477690 | AGGCAGAGGTTGCAG[C/T]GAGCTGAGATCGCGC | 23062 |
rs567557631 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23469228 | ATCGGGAGTTGTGTG[A/G]TCAATAACCGGCATC | 23062 |
rs567602348 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463448 | AGAATCCCTCTGAAA[A/G]GACAGAGGATGGTAA | 23062 |
rs567733169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23495927 | GAGGAATTGTGCCTG[C/T]GCTGCCTACCACCAC | 23062 |
rs567758079 | snp | C/T | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503443 | TTTACTTGTAAGATA[C/T]AGTTACTTAAATGTT | 23062 |
rs567939109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503737 | TTTTCCTATGGGGGG[A/G]AAAAAGATTTATCAT | 23062 |
rs567990826 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466757 | ACTGACATGGTGTGT[C/T]ACAAAGAGCTCCAAG | 23062 |
rs568025889 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511173 | TTTTTCTTTTTTTGA[C/G]ACGGAGTCTCACTCT | 23062 |
rs568063743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504283 | TCTAACCACTCTTGC[A/G]GTGAGGTCTTCAGTT | 23062 |
rs568191925 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23467707 | GATAGGTTCCTGGGA[C/G]AGAAGAGACAGAAGA | 23062 |
rs568217140 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23473151 | GGGCATAAAAATGGT[A/C]TAGGCTTATAAAGTA | 23062 |
rs568273352 | snp | A/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23493643 | AAATGTCCCCTGTTC[A/T]ATCTTGCTATAACTG | 23062 |
rs568294273 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465786 | TCTCTACTAAAAATA[A/C]AAAAATTAGCTGGGC | 23062 |
rs568315033 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23496723 | GCACTTTGGGAAGCC[A/G]AGGCAGGTAGATCAC | 23062 |
rs568332966 | snp | A/G | | | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463202 | GGGAATGGTGCCAGC[A/G]GGAGGGAGAGGATAC | 23062 |
rs568388163 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23487864 | AGGCAGAGCATACCA[C/T]GCAGAAACGAGTACG | 23062 |
rs568617546 | snp | C/T | 1.71337e-05 | 0.00292687 | missense | GGA2 | GRCh38.p7 | 16:23470022 | CCACTTGAAACATGA[C/T]ATCCCAGACAGGCTG | 23062 |
rs568721772 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23494162 | TGGCCCAGATCTCCC[C/T]CCTCCAACCTGCTGT | 23062 |
rs568725957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23502337 | TTACCCCAGGCCGAT[A/G]ATGGTCATGCCACCT | 23062 |
rs568751179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23483700 | TGCCCAGGCTGGAGT[A/G]CAATGGTGTGATCTC | 23062 |
rs568899549 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23477776 | AAACAAAAACACATG[A/C/G]CTTTTGCCTTCCGCC | 23062 |
rs569086564 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23498564 | GAGGCCCCATCTCTA[A/C]AAATATGTTTACAAA | 23062 |
rs569098009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23489348 | CAAGCAGTCCTCTCA[C/T]CTTGGCCTCCCAAGT | 23062 |
rs569101305 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23468543 | CAGTAGTGCGATCTC[A/G]GCTCACTGCAACCTC | 23062 |
rs569127012 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499139 | CACAGCACTGACGGG[A/C]ACCACCTTTTTTTTT | 23062 |
rs569138084 | snp | C/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499631 | TTTGAGAGGCCGAGG[C/T]GGGAAGATCCCGAGT | 23062 |
rs569195966 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23497205 | GTACTGGTTCTGACA[C/G]AGCAGCTCTTTTAGG | 23062 |
rs569301820 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23504970 | AGCCAAACCATCCCA[C/T]GTCAGCTGCCAACCA | 23062 |
rs569380350 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23482353 | AGGTACAGATGAAGT[A/T]AGATTAAAAAAATCA | 23062 |
rs569539430 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23475762 | TACAAAAATTAAAAA[A/T]AAATAAAAAATAAAA | 23062 |
rs569543245 | snp | A/G | 3.29489e-05 | 0.00405874 | intron-variant | GGA2 | GRCh38.p7 | 16:23486807 | TGCAGAGAGTGAACA[A/G]GAAGAGTAGGTGAGA | 23062 |
rs569656944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23490473 | GGAGCGGTGGCTCAC[A/G]CCTGTAATTCCAGCA | 23062 |
rs569738345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23492803 | GACACATGAGACTCA[C/T]GGCTGGCAGCTGAAA | 23062 |
rs569781803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501637 | TCAGCATGAATTTCA[C/T]TGGTATTCGGTGCAC | 23062 |
rs569857716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23472323 | CTCAGCCTCCCAAGT[A/G]GCTGGGACTACAGGC | 23062 |
rs569865718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23479291 | GAGACCAGCTCACTC[C/T]CCTACTCAGAACCCT | 23062 |
rs569875885 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23487854 | TGCAGTTGACAGGCA[A/G]AGCATACCACGCAGA | 23062 |
rs569900725 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23471920 | TCTCTAAAAAAATTT[A/T]AAAAAAAATTAAAAC | 23062 |
rs569958409 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463208 | GGTGCCAGCGGGAGG[A/G]AGAGGATACAAGGAA | 23062 |
rs569973961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500496 | ACAGCAGATGGAACA[C/T]GCTGTTGCCCAATGC | 23062 |
rs569994230 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23463648 | CCACTGTCAGATGTG[C/T]ACACAAACATCTTGG | 23062 |
rs570017546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499963 | GGACTCTGGGCCAGA[C/T]TGGTTCCTGGGAACC | 23062 |
rs570127552 | snp | A/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466554 | CTCTAAATGCAACTG[A/G]CTTTCCATTTTCCAC | 23062 |
rs570173974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23490032 | TGAATCAGAACAGAG[A/G]CTGGCCCTGCCCGCC | 23062 |
rs570257149 | snp | C/T | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511528 | TTTCAGATGGAGTCT[C/T]GCTCTGTCGCCCAGG | 23062 |
rs570333168 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23481446 | GCAAAACTGAGACCG[A/G]GAGAACTGTCAATTC | 23062 |
rs570377149 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23507292 | GGACACTGCCCCCAA[A/C]AGCTGGAGCTTAATA | 23062 |
rs570450298 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23497624 | CTCTCTCCCATGTTC[C/T]GTATCTTAAAATCCT | 23062 |
rs570619125 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467126 | GCCCCAAGACTAACC[A/G]GGTCCCTTTTAAGGT | 23062 |
rs570631813 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510568 | GCCCCCCCTCCACGC[A/G]GGACCGGCCGGAACA | 23062 |
rs570702525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504343 | GCCAGCTTGATCTTC[A/G]TGCTCATAAACTCCT | 23062 |
rs570730920 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23490889 | GGTAGCATTTATCTG[C/T]ACTTCATAGTAAGGT | 23062 |
rs570732741 | in-del | -/T | 0.159951 | 0.233219 | intron-variant | GGA2 | GRCh38.p7 | 16:23508064 | TCTTACTCCGGCTAC[-/T]TTTTTTTTTTTTTTT | 23062 |
rs570811614 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23486843 | ACTCCCTCAGGCCTA[A/G]AGCAGAAGCAGCAGC | 23062 |
rs570821993 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23481150 | TTGGGAGGCCGAGGC[A/G]GGTGGATCACCTGAG | 23062 |
rs570827240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23474547 | ATTTTTTGTAGAGAG[A/G]GGGCTTCGTTATGTT | 23062 |
rs570855466 | snp | C/T | 4.94173e-05 | 0.00497053 | missense | GGA2 | GRCh38.p7 | 16:23488608 | TCTGTTTCCTTACCT[C/T]GGACTTTTCTTCATC | 23062 |
rs570943970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23502466 | TCTGGGTTCAAACCT[C/T]TATCAGAAGATCATT | 23062 |
rs571023276 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23509705 | GCCCAACCAGGGTAA[C/T]ATAATGAGACCCCGT | 23062 |
rs571115097 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23487884 | AAACGAGTACGCAGC[A/G]TGTAGCCTTCCAACA | 23062 |
rs571291415 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23471055 | GGCTGGGGGAGGTCA[A/G]GCCTCAAACTCCCGA | 23062 |
rs571328640 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23463680 | GCATCGCTTGGCTTT[A/G]AAACAAACTGGGGTC | 23062 |
rs571403105 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499248 | CTCCCGGGTTCAAGC[A/G]ATTCTCCGGCCTCAG | 23062 |
rs571409624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23492586 | TCCAGGGGAGGGCAC[A/G]GCAGCTCTGTCCCCT | 23062 |
rs571439360 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23491959 | TCTGGCGCCCAGCCC[C/T]GGAGCCCTTCCTGGG | 23062 |
rs571453013 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | GGA2 | GRCh38.p7 | 16:23506381 | GAAGAAAACAACAAC[A/G]AATACAGCCATGAAG | 23062 |
rs571539361 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23483467 | GGACAGGTAAATAAA[G/T]AAGTTACGTGGAGGC | 23062 |
rs571668590 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | GGA2 | GRCh38.p7 | 16:23481323 | GGTTGCAGCGAGCTG[A/C]GATCGCACCATTGCA | 23062 |
rs571685933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501661 | GGTGCACTAATGCCA[C/T]CTTAAAGAGAGAAAT | 23062 |
rs571779486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23475967 | AAAAGCACTTAAAAT[A/G]TCCACACATAATAAG | 23062 |
rs571787484 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23473756 | AATACAAAAATTTCT[A/G]TATACCCTTCATGTA | 23062 |
rs571908012 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23506102 | CAACAACCCTAAGAA[A/G]AGGTTTTATTACTCT | 23062 |
rs571912859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23508101 | AGAATCTCGCCTTGT[C/T]ACCTAGGCTGGAGTG | 23062 |
rs571917334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23469122 | CCCTCTTAAACGTGG[C/T]ACCCCGAGGCACCTA | 23062 |
rs571987004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23493692 | GAAATAGCTTAGTGA[A/G]GTATGTCAAACCCTG | 23062 |
rs571992578 | snp | A/G | 0.000570152 | 0.0168746 | intron-variant | GGA2 | GRCh38.p7 | 16:23478635 | CTCTTGGGGCAAGAG[A/G]GGAAAGAAAGGGCAA | 23062 |
rs571999310 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23487445 | CAGTGCACAGGACAG[G/T]CCCCAACAACAGAGA | 23062 |
rs572051735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23509384 | TGCGGTCGGCTGTGA[C/T]GACCCCCAGGTAAAC | 23062 |
rs572051865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501042 | ACTTGGGCAATATAT[C/T]ACAACATAAAGCACA | 23062 |
rs572118866 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23506703 | GTCCGGGTGGGCCCA[A/C]TTCGGTTTGCCTCAC | 23062 |
rs572167151 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | GGA2 | GRCh38.p7 | 16:23479345 | CTTGCTCCCAGAGGG[A/G]ACCAGCTCACTCCCC | 23062 |
rs572183209 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464832 | AATACGATCTGGCGA[C/G]AGCAAGGAGGTGGCA | 23062 |
rs572357092 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23484783 | GTAAAATGGCATGGC[C/T]ACTTTGGAAAACAGC | 23062 |
rs572381150 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463909 | GAATTCAAGGCTGCA[C/T]TGAGCTACAATCACG | 23062 |
rs572465424 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23471235 | GCTCACACACACACA[A/C]TATACCACCTTATAT | 23062 |
rs572552890 | in-del | -/A | 0.251859 | 0.249993 | intron-variant | GGA2 | GRCh38.p7 | 16:23496956 | AGCGAGACTCCATCT[-/A]AAAAAAAAAAAAAAA | 23062 |
rs572560970 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500046 | AGTGGAAGGAAGAGG[A/C]GCTCCCTCTGTGCTC | 23062 |
rs572568452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23476121 | GCAGATGATACACAA[A/G]TTATACCAGCTACTA | 23062 |
rs572579622 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499642 | GAGGCGGGAAGATCC[C/T]GAGTAGGGACGGGGT | 23062 |
rs572616860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23492324 | CCCCTGACCGGTGCC[C/T]CCACATCCCCCCACC | 23062 |
rs572699145 | in-del | -/TC | 0.000863711 | 0.0207632 | intron-variant | GGA2 | GRCh38.p7 | 16:23478850 | CTGAGACCCTCCCAT[-/TC]TCTCTCCGGGCCCTG | 23062 |
rs572752879 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23481954 | CAATCTGAACACTGA[C/G]TGAATCTTTGATTAT | 23062 |
rs572782999 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23474171 | CTAGCCAAATTCATC[C/G]ACTCGTTTGAATTCT | 23062 |
rs572816916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23467992 | TGTCCCTCCCTTGGT[C/T]CCCAGCTATGACAAT | 23062 |
rs572858880 | in-del | -/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23508938 | TTTCTCCTTGTCCCC[-/T]GTCTGCATTCCAAGG | 23062 |
rs572920125 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23471888 | CACTCCTGCCTAGGC[A/G]ATGGAGCGAGGCCCC | 23062 |
rs572932188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23496088 | GGGGAATCATTTGAG[A/G]TCAGAAGTTTGAGAC | 23062 |
rs572975642 | snp | C/T | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466421 | AAATATCCACCTCTC[C/T]TGTCCAGCTTGCCTC | 23062 |
rs573011908 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23497020 | CACAGCTACTCAGGA[A/C]GCTGAAGTGGAAAGA | 23062 |
rs573013313 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23463758 | GGCAGGAGGACTGCT[C/T]GAGCCCAGGAGACCA | 23062 |
rs573149936 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23494441 | TAACCCGAGTGGCTG[A/G]GCATGCTCAGTAAAA | 23062 |
rs573238951 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23510154 | ATGCTTGGGGCTCCT[C/G]TCGGGGGACCCCTGG | 23062 |
rs573275617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503196 | GGAATATCCCACTGT[C/T]GATTTGCGATTTCCT | 23062 |
rs573375265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23487928 | ACCTTGTGACTGACC[A/G]AGAACAGTCATGACC | 23062 |
rs573415743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503893 | TCAAGACCAGCCTGA[C/T]CAACATGGAGAAACC | 23062 |
rs573459399 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466335 | GACTTGTCAAACATA[C/T]ACATTCAAGTTCCTA | 23062 |
rs573466432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23480431 | AGCCATCTGCTTTTG[C/T]GTGTAGTCAAAGCTG | 23062 |
rs573544577 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23506806 | AATGGTGGCACTGAC[C/G]AACTTGTTTGCATGT | 23062 |
rs573594130 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23463733 | TAATCCCAGCACTTT[A/G]GGAGGTCAAGGCAGG | 23062 |
rs573698502 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23504927 | CGGCTGTGAGTGAAA[C/T]GGCTCATCCAAGAGT | 23062 |
rs573869673 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23477324 | GGACCCAGTAAGAGA[G/T]AACTGAATCATGGGT | 23062 |
rs573898101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23505147 | CGTGGACCCCAAGAG[C/T]CCGGCAATCATACAA | 23062 |
rs573907224 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | GGA2 | GRCh38.p7 | 16:23477968 | CTTGGCCAGGCAGAC[A/G]GATCACCTGAGGTCA | 23062 |
rs573926762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23490666 | CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAA | 23062 |
rs573937384 | in-del | -/AC | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467269 | CAACCTGAGGCAGGG[-/AC]AGTGTCGCTCGCTGA | 23062 |
rs573946905 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23470362 | GACCCTCCAAACTGA[A/C]CTTTCCCCACCATCC | 23062 |
rs573987607 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23471121 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCACCC | 23062 |
rs574006593 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23492194 | AAGAGACACACTCGC[A/T]GGGTGCACCTGAGTT | 23062 |
rs574034084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23483889 | TGAACTCAGGTCATC[C/T]GCCTGCCTCGGCCTC | 23062 |
rs574073496 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23495219 | TTTCCTTTTTCTTAA[A/C]ATTACATTTAAATGG | 23062 |
rs574132245 | in-del | -/A | 0.00199481 | 0.0315187 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464981 | GGAAAAAGAGCAGTC[-/A]ACGGAGGTAGGTCAC | 23062 |
rs574253561 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23498250 | GTGACACTGCACTCC[A/G]GCCTGGGTGACAAGG | 23062 |
rs574365600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23488101 | AAAATGGATAGGGCC[A/G]GGCTCACTGGCACTG | 23062 |
rs574425811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23488799 | TGGAAACCCCTGGTT[C/T]CTAATACCATGCTAG | 23062 |
rs574431113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23502857 | ACTGCCCCAGAGTCT[A/G]CAAGGGAAACACTTT | 23062 |
rs574432686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23494501 | AAGCAGAGGTGGAGC[A/G]TGCCTGACAAACAGG | 23062 |
rs574521462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23472069 | AAAATTTTAAATGTC[C/T]ACATGTGGCATTTCA | 23062 |
rs574558207 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464845 | GACAGCAAGGAGGTG[G/T]CAGCTTGAGAGAGGT | 23062 |
rs574560020 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23472647 | TGGAGGATGGAGGTT[G/T]TAGTAAGCTGAGATG | 23062 |
rs574577376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23509886 | GCCCCAAACAGACTG[C/T]ATGTCTTGCACGACT | 23062 |
rs574596812 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465539 | GGAGAAAGCCTGTCT[C/T]TATGTATAAGTCTCA | 23062 |
rs574632124 | in-del | -/GTT | | | intron-variant | GGA2 | GRCh38.p7 | 16:23472184 | TTCTTTGTAGCCCTG[-/GTT]TTTTTTTTTTTTTTT | 23062 |
rs574734342 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23479506 | CTCCGAGGGTCCAGC[G/T]CACTCCCCTACTCAC | 23062 |
rs574821827 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23491391 | AGTGCTTTAGTGACA[C/T]AGGTAGCTTGTATTT | 23062 |
rs574923563 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23468481 | GCACCTGGCCGACTT[A/T]ATTTTTTTTTGAGAT | 23062 |
rs574988420 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23486393 | TGCCACCAGCCTCAA[C/G]TCCTCTGAAAAGCAG | 23062 |
rs575062412 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500730 | GCAGGCGGAGGTGGC[A/C]GTAGCGCCACACCCC | 23062 |
rs575100594 | snp | A/G | 0.00136309 | 0.0260708 | intron-variant | GGA2 | GRCh38.p7 | 16:23493547 | CTTGCTGGAGACTGC[A/G]CTGGAACCAAGGCTA | 23062 |
rs575169302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23476375 | GAAGGTAAGCTGCAC[C/T]TTTCCAGAGGCAAAG | 23062 |
rs575250475 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23492458 | AGTTCAAGCCAGCAA[C/T]GATGTGTAAAAAAAC | 23062 |
rs575264143 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23498516 | GAGGATCGCCTGAAC[C/T]CAGGACTTCGTGACA | 23062 |
rs575370622 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23482682 | TCTACCTCTCACACC[C/G]CAATCTCCATGGTCA | 23062 |
rs575449013 | snp | A/G | 0 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23483138 | CAATGGTCCTGACTT[A/G]GAGACTGCAGTTTTG | 23062 |
rs575473263 | in-del | -/A | | | intron-variant | GGA2 | GRCh38.p7 | 16:23484246 | ACCCTGTCTCTACTT[-/A]AAAAAAAAAAAAAAA | 23062 |
rs575496120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23489591 | CAGGGCAACAACCAA[A/G]TAACCTGAAATCTAA | 23062 |
rs575496266 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23497809 | CACATGTACTTGGAC[A/T]CGCTGAGCCTCAGTT | 23062 |
rs575525311 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504012 | CTTGAACCCGGGAGA[C/T]GGAGGTTGCGGTGAG | 23062 |
rs575568729 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511823 | AATCAATCCAAAAGT[A/G]AAGTCAAAGAAGGGC | 23062 |
rs575669021 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23493910 | ATTAGTCACCAACAT[C/G]TAAACACTCAAACAT | 23062 |
rs575785610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23481692 | GCATGAGAATCGCTT[A/G]AACACAGGATGTAAA | 23062 |
rs575856598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23497246 | GAGGCGTTGCTTCTC[A/G]GGGCAGTACTTCTGA | 23062 |
rs575885528 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510737 | TAAGAGACGGGGTCT[C/T]GCTCTGTCACTCAGG | 23062 |
rs575921299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23508029 | TCCTTTTATCTCCTC[C/T]ACCTGAGGCAGCTAC | 23062 |
rs575938645 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23474679 | CTGGTCTCAAACTCC[C/T]GGCCTCAAGTGATCC | 23062 |
rs575958478 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500870 | AAAGTACGCTTTTTT[A/T]GAGAAAATATCAAAT | 23062 |
rs576011870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23467825 | GATACTCTCTTTGGG[A/G]CTACAAACAAGGGGA | 23062 |
rs576152955 | snp | A/G | 8.51861e-05 | 0.00652578 | intron-variant | GGA2 | GRCh38.p7 | 16:23478633 | ATCTCTTGGGGCAAG[A/G]GGGGAAAGAAAGGGC | 23062 |
rs576180152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23470432 | TTTTGAGGAAGATAC[A/G]ATCATTATTAAAATA | 23062 |
rs576189779 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23471146 | GCACCCGGCCAATGC[A/G/T]TTCTTAATTCTACCC | 23062 |
rs576238293 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23485249 | GGAGTTTGGGAAAGG[C/G]GGAATGACTGTTAAT | 23062 |
rs576318604 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | GGA2 | GRCh38.p7 | 16:23507561 | TGAACCTGGGAGGCG[G/T]ACGTTGCAGTGAGCT | 23062 |
rs576351423 | snp | A/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464681 | ACGAAGCAGGAATCA[A/G]GGACCCAATAAGTCT | 23062 |
rs576373413 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23463814 | TTTACGAAAAACTGC[A/G]ACATTAGCTGGGCGT | 23062 |
rs576378234 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | GGA2 | GRCh38.p7 | 16:23491547 | AAAAAAAAAAAAAAA[A/C]ACTCTACCTCAGTGT | 23062 |
rs576442074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23478113 | CTGAGGCAGGAGAAT[C/T]GCTTGAACTCAGGAG | 23062 |
rs576455427 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23481781 | TGAGACTGTCTCAAA[A/T]AAAAGGAAAAAGGAT | 23062 |
rs576487480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23482454 | CGAGATTTTCCACAA[C/T]AAAGAGTTAAAATTC | 23062 |
rs576552455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23505960 | GGTATGGGTATGAGT[C/T]AGTTTCAATTACTTG | 23062 |
rs576710680 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499366 | GGCCAGGCTAGTCTC[A/C/G]AACTACTGACCTCGT | 23062 |
rs576931392 | snp | A/C | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23502199 | GGCATCGGGGCAAGG[A/C]TGTCATTACTCCAAG | 23062 |
rs576932055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503117 | TACCTTTCCTTTCCT[C/T]TTATCGGGAACAATA | 23062 |
rs576971749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23495471 | CCTGACTGCATTTCT[A/G]TTTTTTTGAGACAGA | 23062 |
rs576977009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503821 | GTGTAGTGGCTCATG[C/T]CTGTAATCCCAGCAT | 23062 |
rs577113037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23495968 | ATTGGGCACATGGTA[C/T]GCCCTTACTGAATAT | 23062 |
rs577199175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23473389 | TTGCTCAGACTGAAG[C/T]GCAGTGGCACGATCT | 23062 |
rs577219916 | in-del | -/AAAAC | 0.0023933 | 0.0345097 | intron-variant | GGA2 | GRCh38.p7 | 16:23492468 | GCAATGATGTGTAAA[-/AAAAC]AAAACAAAACAAAAC | 23062 |
rs577220064 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23488288 | GGGCACAAAGTACCC[G/T]TGAAGGAGGAGCAGG | 23062 |
rs577448291 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | GGA2 | GRCh38.p7 | 16:23510052 | CGTAGCCATTGGGGT[A/G]GGGGTCGGGGTCCTG | 23062 |
rs577499909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23494240 | GTGTGGAAGCAAAGC[A/G]CCTCTCGGCTCTCTA | 23062 |
rs577532752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23487309 | AGTGGGGTAGGGGGA[C/T]GTGGGGGTTACTTCT | 23062 |
rs577602220 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23470303 | GACTGAATTCCTCTG[A/C]ACTACCATAATCCAA | 23062 |
rs577674714 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23487320 | GGGATGTGGGGGTTA[A/C]TTCTCCCAGGGGATG | 23062 |
rs577676484 | snp | C/G | | | missense | GGA2 | GRCh38.p7 | 16:23478485 | CTCTTTTCCTCACAG[C/G]AATTCTGACCAGAAA | 23062 |
rs577715072 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23475641 | GGGCACGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 23062 |
rs577717720 | snp | C/T | 0 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23506029 | CTTGGGCACTTACTA[C/T]AAGCATAGTAAGGCA | 23062 |
rs577746534 | snp | A/G | 0 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23491337 | AAAAAAAACCAAAAG[A/G]TTAGTTTTTAGGCAA | 23062 |
rs577777984 | snp | A/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467361 | ACTGCCGATATCCCA[A/G]GCCCTGTGCTACCAC | 23062 |
rs577816693 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23493073 | CTGGGATCTCTCACT[A/G]TCTCTATCAGGAACC | 23062 |
rs577855650 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | GGA2 | GRCh38.p7 | 16:23506779 | CACTTGAGCACCCAA[C/T]ACTCAGGTGGCAATG | 23062 |
rs577898300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23483209 | AAGTGTATGATTTCT[A/G]AAAATAAAATAATCT | 23062 |
rs577910417 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511895 | ATGGAGGCAAAACTG[C/G]CTTTTCGACCGGGGT | 23062 |
rs577929623 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23497370 | AAAACTTCCTCCCGC[C/T]GCGCCAACCCCACTG | 23062 |
rs577935590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23483738 | CGCAACCTCCGCCTC[C/T]TGGGTTCAAATGATT | 23062 |
rs577971087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23477175 | CAGGCTGGTCTTGAA[C/T]TCCAGGGCTCAAGCG | 23062 |
rs577976925 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23497934 | AGCCTAGGAGGTTGA[A/G]ACCAGCCTGAGCAAC | 23062 |
rs578119780 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23475202 | GCCTTTTTTTTTTTT[C/T]TTTTTGATACAGTAT | 23062 |
rs578179794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23471484 | ACAAAACGTGTGGAA[C/T]AGATCTAAATGAGAC | 23062 |
rs578210980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23504644 | CAGGCCACAGCAACC[A/G]CCGTAGGTCTGTTTG | 23062 |
rs578253910 | snp | A/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500967 | ACCTCGTGTTACACC[A/G]TATTGCTAGATAACA | 23062 |
rs745356564 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23476414 | TCTATGAAAATGTTG[C/T]TACATTCACACCTTA | 23062 |
rs745371160 | snp | A/G | 3.29652e-05 | 0.00405974 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23493414 | AAATTTGGCCACCTC[A/G]CTGTGGAACTTCTCC | 23062 |
rs745411406 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23488212 | ATCCATCACCCACAC[G/T]CCCCACGGGCTATCC | 23062 |
rs745496413 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463936 | CACGCCACTGCACTC[C/G]AGCCTGGGCAACAGA | 23062 |
rs745517388 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23477462 | TAAGACACGCCTTTT[A/G]GCTGAGTGTGGTGGC | 23062 |
rs745531556 | snp | A/G | 1.85748e-05 | 0.00304746 | intron-variant | GGA2 | GRCh38.p7 | 16:23470215 | CACTACAAACCCCCC[A/G]GACAGCCAGGCTGGA | 23062 |
rs745554557 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23507213 | CTTCTGAAAACCCAC[A/G]ATATTTCACTTAAGA | 23062 |
rs745558677 | snp | A/G | 1.651e-05 | 0.0028731 | intron-variant | GGA2 | GRCh38.p7 | 16:23493340 | CGACACAGTCAGCAG[A/G]GCCAAGCCCAGGTAC | 23062 |
rs745591269 | in-del | -/GT | | | intron-variant | GGA2 | GRCh38.p7 | 16:23509777 | CACACACACACACGT[-/GT]GTGTGTGTGTTTAAA | 23062 |
rs745622209 | snp | A/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465361 | GCTGATTAGAAGGGA[A/G]TGATGCCATAAACCA | 23062 |
rs745640118 | snp | A/C | 3.84682e-05 | 0.0043855 | intron-variant | GGA2 | GRCh38.p7 | 16:23479027 | TAGACAAATAAGCAA[A/C]TTACTGAAGGTCATG | 23062 |
rs745654986 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23496524 | GAATACCATCTTGAC[C/G]GTTCATAAAACTTCC | 23062 |
rs745672298 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23482579 | GAAGGTACAAAAGCC[C/T]GTGATCCCCTTGAGA | 23062 |
rs745714094 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23494879 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 23062 |
rs745720693 | snp | A/G | 1.65787e-05 | 0.00287907 | intron-variant | GGA2 | GRCh38.p7 | 16:23479725 | CACTCCCCTACTCGC[A/G]CCCATCCTGTGCCTG | 23062 |
rs745724574 | in-del | -/ACCGACACTTTA | 3.42091e-05 | 0.00413562 | intron-variant | GGA2 | GRCh38.p7 | 16:23491850 | GAAGGGACTTGGGAG[-/ACCGACACTTTA]ACTAAAGAGGTAGCT | 23062 |
rs745736973 | snp | C/G | 1.64768e-05 | 0.00287021 | missense | GGA2 | GRCh38.p7 | 16:23486120 | CTCCACCGCACTGAC[C/G]CTCTTGGACACCTTC | 23062 |
rs745748651 | snp | A/C | 1.64969e-05 | 0.00287196 | missense, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23494345 | TTGCGGAGACTGGAT[A/C]TTGTGGGCCAGTAGC | 23062 |
rs745750967 | snp | A/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465837 | TCCCAGCTACTCGAG[A/G]GGCTGAGGCACGAGA | 23062 |
rs745751081 | snp | C/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500416 | TGCGGAGCTGTACTG[C/T]GGCTCTGACATCTAT | 23062 |
rs745804632 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23483479 | AAAGAAGTTACGTGG[A/C]GGCTGGCTCTCCTCC | 23062 |
rs745823263 | snp | C/T | 0.000117474 | 0.00766312 | missense | GGA2 | GRCh38.p7 | 16:23470130 | GCAGAATTCTGAATC[C/T]ATTCCGGTCATACAC | 23062 |
rs745838942 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23497079 | CACTGCACTCCAACC[C/T]GGGTGGGAGAGCAAG | 23062 |
rs745850084 | snp | C/G | 1.64735e-05 | 0.00286993 | intron-variant | GGA2 | GRCh38.p7 | 16:23486697 | CTACTGAACCAACTG[C/G]AAGAATGCCCACCTC | 23062 |
rs745852569 | in-del | -/TA | | | intron-variant | GGA2 | GRCh38.p7 | 16:23489440 | AGATGGGGGTCTCGC[-/TA]TGTTGCCCAGGCTGG | 23062 |
rs745916811 | snp | A/C | 3.33311e-05 | 0.00408221 | intron-variant | GGA2 | GRCh38.p7 | 16:23480610 | TTACAGGCTGCCCCA[A/C]GGCAGAGAAGGCAAG | 23062 |
rs745922578 | snp | C/T | 3.29598e-05 | 0.00405941 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23474947 | CACTTGAGCCAGAGG[C/T]GTATTCTGTGAAGAT | 23062 |
rs745982026 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23491432 | CATGCTGTGGTTTCC[C/T]ATGATTTCCAGGCAA | 23062 |
rs746043962 | snp | A/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466731 | GGCTGGCTGTTGGCC[A/G]ATTCATCATGACTGA | 23062 |
rs746109268 | snp | A/G | 0.000131883 | 0.00811935 | intron-variant | GGA2 | GRCh38.p7 | 16:23491634 | AAGCAAGAAGATACA[A/G]GCCTAGTCAAGAGGA | 23062 |
rs746130243 | snp | A/G | 1.65441e-05 | 0.00287607 | missense | GGA2 | GRCh38.p7 | 16:23479851 | TCCAAGTCAATCAGG[A/G]GGCAGGTCTTCATGC | 23062 |
rs746184190 | snp | A/C | 1.71472e-05 | 0.00292802 | missense | GGA2 | GRCh38.p7 | 16:23467677 | TTGGTTGAATGTCAG[A/C]TTGTACCGTAAGCGG | 23062 |
rs746203936 | snp | C/T | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467516 | TCCGCACTGAAACAC[C/T]GTGATTAGTCCTGAC | 23062 |
rs746215783 | snp | A/G | 0.000126936 | 0.00796566 | intron-variant | GGA2 | GRCh38.p7 | 16:23478753 | GAGGAAGAGGCTTTG[A/G]ACCTCCAAGGCCATG | 23062 |
rs746215853 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23480624 | AAGGCAGAGAAGGCA[A/G]GGAGAAGCTTTCAAA | 23062 |
rs746229845 | snp | A/C | 2.14062e-05 | 0.00327149 | intron-variant | GGA2 | GRCh38.p7 | 16:23495830 | AGGAAGAAATTTACA[A/C]CCCTCCCCATACACA | 23062 |
rs746294032 | in-del | -/CAAA | | | intron-variant | GGA2 | GRCh38.p7 | 16:23509875 | GATCTTTCTCAGCCC[-/CAAA]CAGACTGCATGTCTT | 23062 |
rs746297665 | in-del | -/AGA | 1.82259e-05 | 0.00301871 | intron-variant | GGA2 | GRCh38.p7 | 16:23467717 | TGGGACAGAAGAGAC[-/AGA]AGATGTCAAATCAGT | 23062 |
rs746299571 | snp | A/T | 1.66629e-05 | 0.00288638 | intron-variant | GGA2 | GRCh38.p7 | 16:23468855 | GTTCAGGGGCCCCCA[A/T]CTCCCTGCTACCACA | 23062 |
rs746316111 | snp | C/T | 1.72113e-05 | 0.00293348 | intron-variant | GGA2 | GRCh38.p7 | 16:23478543 | AGACCAGGGTATGAA[C/T]GACCATCAGCCACAG | 23062 |
rs746388537 | snp | A/G | 1.67248e-05 | 0.00289173 | intron-variant | GGA2 | GRCh38.p7 | 16:23478636 | TCTTGGGGCAAGAGG[A/G]GAAAGAAAGGGCAAG | 23062 |
rs746405795 | snp | A/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501000 | ACAGTCAGCCAGCCT[A/G]ATCTTTGACACACAT | 23062 |
rs746425761 | snp | G/T | 1.65781e-05 | 0.00287902 | missense, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23495715 | GGGTCAGTGTTCACC[G/T]GCTCACAGAAATTCT | 23062 |
rs746449503 | in-del | -/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499489 | CTCTCTGAGGTTAAA[-/T]TACGTTCCAAACCCT | 23062 |
rs746495375 | in-del | -/AA | 3.55322e-05 | 0.00421483 | intron-variant | GGA2 | GRCh38.p7 | 16:23470188 | AAAGGGCACAAGCAG[-/AA]GGTTTAACACCACTA | 23062 |
rs746500766 | snp | C/G | 9.41487e-05 | 0.00686043 | intron-variant | GGA2 | GRCh38.p7 | 16:23478676 | AGCTCCTGGGCAGAC[C/G]TCCAGGAAGCAGGAG | 23062 |
rs746506375 | snp | C/G/T | 6.65484e-05 | 0.00576805 | intron-variant | GGA2 | GRCh38.p7 | 16:23486005 | GCCCCCTGTGTTACA[C/G/T]CTGTATTACCTGCAG | 23062 |
rs746561948 | snp | C/G | | | missense | GGA2 | GRCh38.p7 | 16:23479880 | GCAGCCTGCTGGATT[C/G]TGAAAGACTAGAAAG | 23062 |
rs746570957 | snp | A/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499880 | GGGGTGGGGCCGCTG[A/G]CAGGGCGGGGCCTGG | 23062 |
rs746588551 | snp | A/C | 0.000116643 | 0.00763596 | intron-variant | GGA2 | GRCh38.p7 | 16:23478776 | AGGCCATGATCCCAC[A/C]GGGACAGTGCAGGAG | 23062 |
rs746588777 | snp | A/T | 1.65045e-05 | 0.00287263 | missense | GGA2 | GRCh38.p7 | 16:23493439 | TTCTCCCCACAGTGG[A/T]TCATGCACATCTCCA | 23062 |
rs746618152 | in-del | -/T | 8.79546e-05 | 0.00663096 | intron-variant | GGA2 | GRCh38.p7 | 16:23478730 | GTATCAGCCAGACAG[-/T]TATGGGTGAGGAAGA | 23062 |
rs746632948 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23475835 | CTCAGGAGGCTGAGG[A/C]AGGAGAATGGCTAGA | 23062 |
rs746656226 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23474736 | GGATTACAGGCGTGA[G/T]TCACCATACCTGGCC | 23062 |
rs746672620 | snp | A/C | 1.69674e-05 | 0.00291263 | intron-variant | GGA2 | GRCh38.p7 | 16:23483012 | TACACGACCTGAAAG[A/C]GCAGAGCTTGGTTCA | 23062 |
rs746752217 | snp | A/C | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464450 | TCAGGCATCAGGAAG[A/C]CATTCAGAATTTTTC | 23062 |
rs746755625 | snp | C/T | 6.21214e-05 | 0.00557287 | intron-variant | GGA2 | GRCh38.p7 | 16:23493609 | TTTTGATGAAGAGGA[C/T]GTTTTCAGATCAAGA | 23062 |
rs746788253 | snp | A/C | 1.6664e-05 | 0.00288647 | intron-variant | GGA2 | GRCh38.p7 | 16:23474855 | AGCTGGGAGTCTAAT[A/C]GATTCCCAGGGAAAA | 23062 |
rs746880169 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23505612 | ACTCCTCTGGGAACA[A/G]CCCCTCTCCTCAATT | 23062 |
rs746884919 | snp | A/G | 3.29484e-05 | 0.00405871 | intron-variant | GGA2 | GRCh38.p7 | 16:23486798 | GTCAGAAGCTGCAGA[A/G]AGTGAACAGGAAGAG | 23062 |
rs747030576 | snp | C/T | 1.76746e-05 | 0.0029727 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23478376 | GACTCACAGAGGGCA[C/T]GGAGCTGGCTGTGCT | 23062 |
rs747056837 | snp | A/G | 0.000197765 | 0.00994201 | intron-variant | GGA2 | GRCh38.p7 | 16:23494264 | CTCTCTATAGCACAA[A/G]GACAGGAAAGGTTAG | 23062 |
rs747120425 | snp | A/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23502578 | CACACTGCAACTCAC[A/G]TTTTCCAGTGCACCT | 23062 |
rs747170177 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23477142 | TTTTTTGTAGAGATG[A/G]GGTTTTGCCATATCT | 23062 |
rs747271425 | in-del | -/CC | 0.000451064 | 0.0150109 | intron-variant | GGA2 | GRCh38.p7 | 16:23468848 | CTTACAGTTCAGGGG[-/CC]CCCCCATCTCCCTGC | 23062 |
rs747279159 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23491180 | GGTATGGTGGCACAC[A/G]CCTGTAGTCCCAGCT | 23062 |
rs747321141 | snp | A/G | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511437 | GTGCTGGGATTACAG[A/G]GGTGAGCCACCACGC | 23062 |
rs747334082 | snp | C/T | 1.69075e-05 | 0.00290748 | intron-variant | GGA2 | GRCh38.p7 | 16:23469025 | AAAACCAACATGTAA[C/T]TCATTCCTAACCACA | 23062 |
rs747360402 | snp | A/G | 1.7268e-05 | 0.00293832 | intron-variant | GGA2 | GRCh38.p7 | 16:23479926 | AGAAGTCAGTTGGAC[A/G]TGAGAGCAAAGTCTC | 23062 |
rs747366123 | snp | G/T | 1.64795e-05 | 0.00287045 | intron-variant | GGA2 | GRCh38.p7 | 16:23491661 | AGGAAATAAGACACA[G/T]TAAGGCAAGTCAGAC | 23062 |
rs747368917 | snp | A/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465834 | TAGTCCCAGCTACTC[A/G]AGAGGCTGAGGCACG | 23062 |
rs747382259 | snp | A/C | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504155 | CAATCCAGGTTGGCA[A/C]GATCATCTACACCAT | 23062 |
rs747415623 | snp | C/T | 6.8299e-05 | 0.00584336 | intron-variant | GGA2 | GRCh38.p7 | 16:23478985 | GAGTAATGCCACACC[C/T]ATCCTTTCTAGGACA | 23062 |
rs747526759 | snp | C/G | 1.65979e-05 | 0.00288074 | intron-variant | GGA2 | GRCh38.p7 | 16:23468878 | CTACCACAGACACTG[C/G]AACATACTTTGTGTG | 23062 |
rs747560419 | snp | C/G | 1.64732e-05 | 0.0028699 | missense | GGA2 | GRCh38.p7 | 16:23488680 | GTAAGATTTTATCCA[C/G]TGGTAGTTTAGGGTC | 23062 |
rs747578342 | snp | A/C | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466368 | ACACAGTAGGTGCTA[A/C]GTGGGAATTGATTAT | 23062 |
rs747590538 | in-del | -/CTT | 1.64808e-05 | 0.00287057 | cds-indel | GGA2 | GRCh38.p7 | 16:23486132 | GACCCTCTTGGACAC[-/CTT]CTCCGATTTTTCTTG | 23062 |
rs747635091 | snp | C/T | 1.65762e-05 | 0.00287886 | missense | GGA2 | GRCh38.p7 | 16:23468896 | CATACTTTGTGTGGA[C/T]TGTCAAGCAGCAGCA | 23062 |
rs747671377 | snp | A/C/G | 5.00725e-05 | 0.00500341 | intron-variant | GGA2 | GRCh38.p7 | 16:23478874 | GGGCCCTGGGAAGGG[A/C/G]ATCCTTACCATGCCT | 23062 |
rs747694452 | snp | C/T | 1.6525e-05 | 0.00287441 | missense | GGA2 | GRCh38.p7 | 16:23486023 | GTATTACCTGCAGGG[C/T]CTCCTGGTCGGGCGG | 23062 |
rs747719253 | snp | C/T | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511150 | TGCATTTATTTTTTA[C/T]TTTTCTTTTTTTCTT | 23062 |
rs747722203 | snp | A/G | 3.59648e-05 | 0.00424041 | intron-variant | GGA2 | GRCh38.p7 | 16:23469945 | CCCAGAAAAGAACCT[A/G]GCACTCAAAAACGAC | 23062 |
rs747780261 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23485339 | TTGCTTTTATGGTAT[A/G]TTAATTATCTCATAA | 23062 |
rs747786370 | snp | A/G | 0.000141285 | 0.00840372 | intron-variant | GGA2 | GRCh38.p7 | 16:23478789 | ACCGGGACAGTGCAG[A/G]AGCACCTCTCTGCTC | 23062 |
rs747907995 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23504991 | CTGCCAACCAACCAC[C/T]GGGGTCATGACCCTG | 23062 |
rs747948728 | snp | C/T | 2.40162e-05 | 0.00346519 | intron-variant | GGA2 | GRCh38.p7 | 16:23493518 | TCCCAGGCTCCCCTC[C/T]AGGCTGGTAATCACT | 23062 |
rs748011199 | snp | G/T | 1.65405e-05 | 0.00287576 | missense | GGA2 | GRCh38.p7 | 16:23479849 | CCTCCAAGTCAATCA[G/T]GGGGCAGGTCTTCAT | 23062 |
rs748104955 | snp | G/T | 0.000164788 | 0.00907562 | missense | GGA2 | GRCh38.p7 | 16:23474939 | GGGACAAACACTTGA[G/T]CCAGAGGTGTATTCT | 23062 |
rs748138963 | snp | C/T | 3.30387e-05 | 0.00406427 | missense | GGA2 | GRCh38.p7 | 16:23493449 | AGTGGTTCATGCACA[C/T]CTCCAGCACCTGCAC | 23062 |
rs748146470 | snp | A/C | 3.16691e-05 | 0.00397914 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467550 | ACAGCAAAAGTAACG[A/C]CAGCCTAAGCTTGAA | 23062 |
rs748217389 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | GGA2 | GRCh38.p7 | 16:23486727 | CCTTGACCAAATTCT[C/T]GATTAACCGGTTTGC | 23062 |
rs748217530 | snp | C/G | 1.74333e-05 | 0.00295235 | intron-variant | GGA2 | GRCh38.p7 | 16:23495662 | TGTGGGGTGCCCCCA[C/G]AGTCAACTATGTGTG | 23062 |
rs748232799 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23469896 | TTCAGTTAGTTTGAG[C/T]GAAGATTCTTTCCTT | 23062 |
rs748240676 | in-del | -/ACTG | | | intron-variant | GGA2 | GRCh38.p7 | 16:23473199 | AAACATTCTATACAC[-/ACTG]TGGTATCAAATTATT | 23062 |
rs748279924 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23482456 | AGATTTTCCACAATA[A/G]AGAGTTAAAATTCTT | 23062 |
rs748343549 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23470269 | GATGCTGTTGCTTCT[C/G]CATGCAGAACATGTC | 23062 |
rs748401420 | snp | C/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23502352 | AATGGTCATGCCACC[C/T]AGGGAAGCAGTAAAA | 23062 |
rs748402696 | snp | C/T | 1.69063e-05 | 0.00290738 | intron-variant | GGA2 | GRCh38.p7 | 16:23478517 | CTGTCAAATCAGGAA[C/T]GGCTAAAATAAGACC | 23062 |
rs748410622 | snp | C/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500981 | CATATTGCTAGATAA[C/G]AGAACAGTCAGCCAG | 23062 |
rs748411780 | snp | A/G | 1.65029e-05 | 0.00287248 | missense, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23494352 | GACTGGATCTTGTGG[A/G]CCAGTAGCCAGGGCG | 23062 |
rs748543582 | in-del | -/CT | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23463618 | TTTATCTATAATTCC[-/CT]GACCCAAAGATTACC | 23062 |
rs748546853 | in-del | -/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23487303 | GTTTTCAGTGGGGTA[-/G]GGGGATGTGGGGGTT | 23062 |
rs748565025 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23489737 | TCTGGAGGCTGCAAC[A/C]AAAAGAAAATAAGCT | 23062 |
rs748638104 | snp | A/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465739 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 23062 |
rs748787827 | snp | G/T | 0.00060939 | 0.0174449 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23491764 | GTATTTCAATGACTC[G/T]TCCTTTAACTTTTCC | 23062 |
rs748797331 | snp | C/G | 3.30978e-05 | 0.0040679 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23470065 | CATCATGGTCAAGAG[C/G]AGCACCTGTACCTCT | 23062 |
rs748878746 | snp | C/T | 1.66438e-05 | 0.00288472 | missense | GGA2 | GRCh38.p7 | 16:23478887 | GGCATCCTTACCATG[C/T]CTGTAACAGGAGCAT | 23062 |
rs748880837 | snp | A/G | 1.6476e-05 | 0.00287014 | intron-variant | GGA2 | GRCh38.p7 | 16:23486684 | TCAAATGCTACTTCT[A/G]CTGAACCAACTGGAA | 23062 |
rs748883234 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23507402 | GGAGGCCAAGACTGG[C/G]AGATAACTTGAGGTC | 23062 |
rs748912771 | snp | C/T | 1.79654e-05 | 0.00299706 | intron-variant | GGA2 | GRCh38.p7 | 16:23469957 | CCTGGCACTCAAAAA[C/T]GACAGCCATTACTGA | 23062 |
rs748958549 | snp | C/T | 0.000161773 | 0.00899224 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465443 | TCCAACACCTAAGCA[C/T]AGTAGTACCACTGGG | 23062 |
rs748968554 | snp | C/G | 2.37928e-05 | 0.00344903 | intron-variant | GGA2 | GRCh38.p7 | 16:23478989 | AATGCCACACCCATC[C/G]TTTCTAGGACATCCA | 23062 |
rs748983201 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23488247 | GCACCTTCTTTCCCC[C/T]AGGAAGGCTGTGCAC | 23062 |
rs749049044 | in-del | -/AG | | | intron-variant | GGA2 | GRCh38.p7 | 16:23489871 | AGCTAGAGAAAAAAC[-/AG]GGGAGAAAAAACAAA | 23062 |
rs749055997 | in-del | -/TGA | | | intron-variant | GGA2 | GRCh38.p7 | 16:23497178 | CCTGCCCAGCCTCTC[-/TGA]TGAGAAACCGTACTG | 23062 |
rs749117944 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23483780 | AGCCTCCTGAGTAGC[A/C]GGGATTACAGGCATG | 23062 |
rs749128501 | snp | A/C | 1.64887e-05 | 0.00287125 | intron-variant | GGA2 | GRCh38.p7 | 16:23493527 | CCCCTCCAGGCTGGT[A/C]ATCACTTGCTGGAGA | 23062 |
rs749160907 | in-del | -/AG | 4.94222e-05 | 0.00497078 | intron-variant | GGA2 | GRCh38.p7 | 16:23486795 | CTTGTCAGAAGCTGC[-/AG]AGAGTGAACAGGAAG | 23062 |
rs749267381 | snp | A/G | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503911 | ACATGGAGAAACCCC[A/G]TCTCTACTAAAAATA | 23062 |
rs749286465 | snp | C/G | 1.6483e-05 | 0.00287076 | intron-variant | GGA2 | GRCh38.p7 | 16:23494253 | GCGCCTCTCGGCTCT[C/G]TATAGCACAAGGACA | 23062 |
rs749293348 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23469775 | GCAGAGTCAAGAGAT[A/G]CAGATTCTTAAGGCA | 23062 |
rs749311344 | snp | A/C/G | 6.58908e-05 | 0.0057395 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23488651 | GGAGCTCTTGGGCCA[A/C/G]GGAGATGGTGGGGGT | 23062 |
rs749356441 | snp | A/G | 1.65367e-05 | 0.00287543 | intron-variant | GGA2 | GRCh38.p7 | 16:23479751 | GCCTGCTCCCCACAA[A/G]CACCTGCCCTCACCC | 23062 |
rs749382158 | in-del | -/A | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500741 | TGGCAGTAGCGCCAC[-/A]CCCCACTGCTGTGGA | 23062 |
rs749418777 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23469700 | GACCATGCAACCCTG[A/G]AGCTGTGGGTAGCCA | 23062 |
rs749431424 | snp | C/G | 0.000143838 | 0.0084793 | intron-variant | GGA2 | GRCh38.p7 | 16:23493539 | GGTAATCACTTGCTG[C/G]AGACTGCGCTGGAAC | 23062 |
rs749473659 | snp | G/T | 5.06496e-05 | 0.00503212 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23495690 | GTGTGAGAAGTTACC[G/T]TACCCATTGGGGTCA | 23062 |
rs749526427 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23467816 | AATACCTGGGATACT[A/C]TCTTTGGGACTACAA | 23062 |
rs749539729 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23482427 | GTTTTACTATTCCCC[C/T]CTCTCATGTTTCGAG | 23062 |
rs749561543 | snp | A/G | 1.64743e-05 | 0.00287 | intron-variant | GGA2 | GRCh38.p7 | 16:23486808 | GCAGAGAGTGAACAG[A/G]AAGAGTAGGTGAGAC | 23062 |
rs749607147 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23488278 | AAAAGGGAGAGGGCA[A/C]AAAGTACCCTTGAAG | 23062 |
rs749646978 | snp | C/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23502284 | GAAATGAGGCCCCTA[C/T]GTCATGATTATAAAG | 23062 |
rs749662302 | snp | A/C | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501118 | CACTTTCACAAGAGA[A/C]GGTTCCAGGGAAATC | 23062 |
rs749688834 | in-del | -/TTT | | | intron-variant | GGA2 | GRCh38.p7 | 16:23472186 | CTTTGTAGCCCTGGT[-/TTT]TTTTTTTTTTTTTTT | 23062 |
rs749721440 | in-del | -/CTC | 1.75262e-05 | 0.0029602 | cds-indel | GGA2 | GRCh38.p7 | 16:23467634 | GGAAGTCTTTCACTT[-/CTC]CTACTTCGCTGAAAG | 23062 |
rs749723996 | snp | A/C | 1.66142e-05 | 0.00288216 | intron-variant | GGA2 | GRCh38.p7 | 16:23478629 | TGACATCTCTTGGGG[A/C]AAGAGGGGAAAGAAA | 23062 |
rs749739332 | snp | A/C | 2.24661e-05 | 0.0033515 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467588 | GTCCATCTTGTGAAA[A/C]GTTAGGCTGCGCCCA | 23062 |
rs749746189 | snp | A/T | 1.65326e-05 | 0.00287507 | intron-variant | GGA2 | GRCh38.p7 | 16:23480805 | TCAGAACCCCCTGGT[A/T]TGGCAACCAACAATC | 23062 |
rs749758712 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23477540 | TGAGGTCAAGAGATC[A/G]AGACAATCCTGGCTA | 23062 |
rs749811871 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23489286 | GTCTCCCAGGCTAGA[A/C]TGCAGTGGTGTGATC | 23062 |
rs749823171 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23476540 | AAATACATCCATGCA[A/G]TAAATTGTAATGTAG | 23062 |
rs749863230 | snp | G/T | 1.69697e-05 | 0.00291283 | intron-variant | GGA2 | GRCh38.p7 | 16:23479904 | TAGAAAGCCCAGGGT[G/T]AGGAAGAGAAGTCAG | 23062 |
rs749914872 | snp | A/G | 4.94458e-05 | 0.00497197 | missense | GGA2 | GRCh38.p7 | 16:23474916 | TACTGGGCTTAACAG[A/G]CTCCAAAGGGACAAA | 23062 |
rs749935921 | snp | A/C | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503014 | TTTGTTACACCCTGA[A/C]TCCTCATCTTTCCTT | 23062 |
rs749937131 | snp | A/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501684 | AGAGAAATTAACATT[A/G]TAAGATCCTAAACTT | 23062 |
rs750002815 | snp | G/T | 1.64811e-05 | 0.00287059 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23474980 | GGAAGGAGCCAACGG[G/T]CCAGCCTCCCAGGAC | 23062 |
rs750044053 | snp | C/G | | | missense | GGA2 | GRCh38.p7 | 16:23478422 | AAATTCCTGTCTGCA[C/G]AAGGGTTCTGAACAC | 23062 |
rs750101061 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23490374 | GATTTGATCACTACA[C/T]ATTGTATGCATGTAC | 23062 |
rs750103759 | snp | C/T | 1.65083e-05 | 0.00287296 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23479817 | CACAGTCCCCATCTG[C/T]GCAGGTCCATTGTCC | 23062 |
rs750145020 | snp | C/T | 1.74967e-05 | 0.00295771 | missense | GGA2 | GRCh38.p7 | 16:23467634 | GGAAGTCTTTCACTT[C/T]TCCTACTTCGCTGAA | 23062 |
rs750167535 | in-del | -/ACAC | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467388 | CCACCCTCTCCCCGA[-/ACAC]ACACACACACACACA | 23062 |
rs750209165 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23479611 | CTGACTCCCTCAGCA[C/G]CAAGCACGTGCTCCC | 23062 |
rs750283251 | snp | C/G | 1.815e-05 | 0.00301242 | intron-variant | GGA2 | GRCh38.p7 | 16:23467714 | TCCTGGGACAGAAGA[C/G]ACAGAAGATGTCAAA | 23062 |
rs750287031 | in-del | GATATGGAGTCTCGCTCTG/TTTTTTTGGTGT | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499163 | TTTTTTTTTTTTTTT[lengthTooLong]TCACCCGGGCTGGTG | 23062 |
rs750321141 | snp | A/C | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499448 | CACACCCGGCCGGCA[A/C]CAGCTTTCTTTAAGA | 23062 |
rs750334506 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23484640 | ATAGGAAATAAATAA[A/G]CCATCAAGAAACAGA | 23062 |
rs750340970 | snp | A/G | 2.3878e-05 | 0.00345521 | intron-variant | GGA2 | GRCh38.p7 | 16:23478597 | GAGCCCACCCAAGCT[A/G]CTGTGGCCCAGACTG | 23062 |
rs750392949 | snp | C/T | 1.66843e-05 | 0.00288823 | intron-variant | GGA2 | GRCh38.p7 | 16:23494429 | GCAAAAAGAAACTAA[C/T]CCGAGTGGCTGAGCA | 23062 |
rs750495240 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23491723 | AATCTTGATGTCTTC[C/T]GGAAACCAGACTGTC | 23062 |
rs750526117 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23505490 | CATGTGGAATAATGA[A/C]CAAAATACATGAAGT | 23062 |
rs750586806 | snp | C/T | 1.64887e-05 | 0.00287125 | missense | GGA2 | GRCh38.p7 | 16:23480756 | TGAGGAGGTCATTTG[C/T]CTGGAGAATTTCCGC | 23062 |
rs750614316 | snp | A/G | 0.000268061 | 0.011574 | utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23510440 | ACGCTGCGGCCGCGG[A/G]CGCCACTGCCTCTTC | 23062 |
rs750615667 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23494234 | GGATCTGTGTGGAAG[A/C]AAAGCGCCTCTCGGC | 23062 |
rs750685593 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23506660 | CCCAAGATGTCACTC[C/G]TGCAAAGGTTGAGAA | 23062 |
rs750719756 | in-del | -/GGA | 1.66846e-05 | 0.00288826 | cds-indel | GGA2 | GRCh38.p7 | 16:23478457 | GCCTGGCAGCGTGCT[-/GGA]GGAGGGATTCCTCTT | 23062 |
rs750759673 | snp | C/T | 1.64768e-05 | 0.00287021 | missense | GGA2 | GRCh38.p7 | 16:23486062 | CTGGCCTGCGGTACA[C/T]GCTCAGCATCTCCTG | 23062 |
rs750845645 | snp | G/T | 3.53782e-05 | 0.00420569 | intron-variant | GGA2 | GRCh38.p7 | 16:23478828 | GTGCTGCCTCACAAG[G/T]GCAGGTCTGAGACCC | 23062 |
rs750850805 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23470520 | GTAATCCCAGCACTT[C/T]AGGAGGCCAAGGCGG | 23062 |
rs750893125 | in-del | -/C | 1.64936e-05 | 0.00287168 | frameshift-variant | GGA2 | GRCh38.p7 | 16:23480665 | GAGACAGGGATGTCT[-/C]CCAATGAGCTGGTCA | 23062 |
rs750916561 | snp | C/T | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23463700 | AAACTGGGGTCAGGA[C/T]ATGGTGGCTCATGCC | 23062 |
rs750954024 | snp | C/T | 1.67981e-05 | 0.00289806 | intron-variant | GGA2 | GRCh38.p7 | 16:23485984 | CCACTTTAGTAAACA[C/T]GTGCAGCCCCCTGTG | 23062 |
rs750966415 | snp | A/C | 0.00171057 | 0.0291952 | intron-variant | GGA2 | GRCh38.p7 | 16:23493563 | CTGGAACCAAGGCTA[A/C]CCCTGCCTCAAGCCT | 23062 |
rs750990214 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23469272 | CAACAGCCAGGGCAC[A/G]TCTTGGGTTGAATTC | 23062 |
rs751014418 | snp | C/T | 0.00126279 | 0.0250958 | intron-variant | GGA2 | GRCh38.p7 | 16:23493580 | CCTGCCTCAAGCCTA[C/T]GAGGACACTGAAGTT | 23062 |
rs751048578 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23469207 | TTCCTTCCACACACA[C/G]AATGGATCGGGAGTT | 23062 |
rs751100341 | snp | C/T | 1.64746e-05 | 0.00287002 | missense | GGA2 | GRCh38.p7 | 16:23486085 | ATCTCCTGCAGCACC[C/T]TCACATGGCTTCGCA | 23062 |
rs751215565 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23488861 | ACCCAGTGTATGAAC[A/G]AAGTTTTGCATCATC | 23062 |
rs751236894 | snp | C/G | 1.64866e-05 | 0.00287106 | missense | GGA2 | GRCh38.p7 | 16:23475000 | CCTCCCAGGACCAAC[C/G]TGGAGAGGACTTAGT | 23062 |
rs751288609 | snp | C/T | 3.30355e-05 | 0.00406407 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23479832 | CGCAGGTCCATTGTC[C/T]ACCTCCAAGTCAATC | 23062 |
rs751288694 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23477394 | GAGACCTGATGGTTT[C/T]ATAAGGGGAAACCCT | 23062 |
rs751330586 | snp | A/G | 1.66502e-05 | 0.00288527 | intron-variant | GGA2 | GRCh38.p7 | 16:23488733 | GCAATTTACAAAGTT[A/G]AGACACCGATATGGT | 23062 |
rs751376966 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23490197 | TAGCTAGCCCCCAAC[C/T]TAAACATCAGCTAAC | 23062 |
rs751390062 | in-del | -/TT | | | intron-variant | GGA2 | GRCh38.p7 | 16:23470827 | AATGAAATAAATGCT[-/TT]TTTTTTTTTTTTTTT | 23062 |
rs751436865 | snp | C/T | 3.60555e-05 | 0.00424576 | intron-variant | GGA2 | GRCh38.p7 | 16:23495800 | AATAAATAATAAAGT[C/T]AGAGAGTACATAATA | 23062 |
rs751524875 | snp | C/T | 0.000301523 | 0.0122748 | synonymous-codon, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23510388 | GGTTCCCGCCACAGC[C/T]GCCGCCACCGCGGTC | 23062 |
rs751579007 | snp | A/G | 8.81127e-05 | 0.00663691 | missense | GGA2 | GRCh38.p7 | 16:23478377 | ACTCACAGAGGGCAC[A/G]GAGCTGGCTGTGCTG | 23062 |
rs751659774 | snp | A/G | 1.65562e-05 | 0.00287712 | missense | GGA2 | GRCh38.p7 | 16:23482928 | GAAAACTTACCGAGT[A/G]CATCATCGTCATCAG | 23062 |
rs751719704 | snp | A/C | 1.67756e-05 | 0.00289612 | missense | GGA2 | GRCh38.p7 | 16:23478482 | TTCCTCTTTTCCTCA[A/C]AGCAATTCTGACCAG | 23062 |
rs751749141 | snp | C/T | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504498 | GACATACTGATAACA[C/T]GGAGAGATGGCTATC | 23062 |
rs751749491 | snp | A/G | 1.65526e-05 | 0.00287681 | missense | GGA2 | GRCh38.p7 | 16:23482970 | GCCAACCGGAACAGC[A/G]TGGGCCGCAGCTTTT | 23062 |
rs751768029 | snp | C/G | 1.6473e-05 | 0.00286988 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23491732 | GTCTTCCGGAAACCA[C/G]ACTGTCCAACTGAAG | 23062 |
rs751855312 | snp | A/G | 8.2837e-05 | 0.00643519 | intron-variant | GGA2 | GRCh38.p7 | 16:23493312 | GCCAGGAGTTTGACA[A/G]TGGGCGTAGGTGCGA | 23062 |
rs751888914 | snp | C/T | 1.97744e-05 | 0.00314433 | intron-variant | GGA2 | GRCh38.p7 | 16:23478966 | CCACCTGCTTCCAGA[C/T]GAAGAGTAATGCCAC | 23062 |
rs751938548 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23493081 | TCTCACTGTCTCTAT[C/T]AGGAACCTGTGCCTC | 23062 |
rs751943310 | in-del | -/CGCGGG | 0.000796284 | 0.0199376 | utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23510434 | CCCCGACGCTGCGGC[-/CGCGGG]CGCGGGCGCCACTGC | 23062 |
rs751978774 | snp | C/G | 1.69548e-05 | 0.00291154 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23470029 | AAACATGATATCCCA[C/G]ACAGGCTGGGGAGCC | 23062 |
rs752012344 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23493977 | TCATACCTGCCAACA[A/G]CTAGTGGGCCCTGTG | 23062 |
rs752022590 | snp | C/T | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467475 | TTGACACCCAGAGCC[C/T]GACGTCAGGATAGGA | 23062 |
rs752029195 | in-del | -/C | 1.89437e-05 | 0.00307758 | intron-variant | GGA2 | GRCh38.p7 | 16:23483054 | AGGCACCCCATAACG[-/C]CCCCCCTCCAGGGCC | 23062 |
rs752063426 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23481224 | TTTCTACTAAAAATA[C/T]AAAAAATCAGCCGTG | 23062 |
rs752075570 | snp | A/G | 0.000151175 | 0.0086928 | intron-variant | GGA2 | GRCh38.p7 | 16:23478859 | TCCCATTCTCTCTCC[A/G]GGCCCTGGGAAGGGC | 23062 |
rs752230197 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23481013 | TACACCTGTACTGTC[C/T]AGAGTAATGGCCAGC | 23062 |
rs752233620 | in-del | -/AG | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467085 | AAGGTCTTTCTTGGA[-/AG]AGAGTGCCCAAGTAG | 23062 |
rs752251899 | in-del | -/AAC | | | intron-variant | GGA2 | GRCh38.p7 | 16:23473127 | ATCAAGTTTTTAAAG[-/AAC]AACTAAGGGCATAAA | 23062 |
rs752321425 | snp | C/T | 1.64732e-05 | 0.0028699 | missense | GGA2 | GRCh38.p7 | 16:23486757 | CAGCCTGAAGGTCCT[C/T]GGGGTGGTTGCTCTT | 23062 |
rs752422004 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23487667 | GATTGTTTCTCAGAA[A/G]TCACACCATACCTCC | 23062 |
rs752425706 | snp | C/T | 1.64852e-05 | 0.00287094 | missense, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23494323 | AGGCATAAAGAGCTT[C/T]CTTCTCTTGCGGAGA | 23062 |
rs752452922 | snp | A/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467311 | CATGACTGTAGCAGA[A/G]ATGATGATGATGAGA | 23062 |
rs752455578 | snp | A/G | 1.64836e-05 | 0.0028708 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23480748 | TCCTTGGGTGAGGAG[A/G]TCATTTGCCTGGAGA | 23062 |
rs752479180 | snp | A/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500769 | GGAGCCTGCCCAGTC[A/G]GATTTAGGAGCCCGC | 23062 |
rs752582510 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23477183 | TCTTGAACTCCAGGG[A/C]TCAAGCGATCCACCT | 23062 |
rs752597627 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | GGA2 | GRCh38.p7 | 16:23491713 | AAGCGTCTCGAATCT[C/T]GATGTCTTCCGGAAA | 23062 |
rs752637596 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23475533 | TCATACCTCAGCTTC[C/T]TCATCTGTTAAATGG | 23062 |
rs752649954 | snp | A/C | 3.53394e-05 | 0.00420339 | intron-variant | GGA2 | GRCh38.p7 | 16:23479939 | ACATGAGAGCAAAGT[A/C]TCCACATAAATCCTA | 23062 |
rs752791609 | snp | A/C | 2.66244e-05 | 0.00364849 | intron-variant | GGA2 | GRCh38.p7 | 16:23478606 | CAAGCTGCTGTGGCC[A/C]AGACTGGTGACATCT | 23062 |
rs752791823 | snp | A/C/G/T | 3.29626e-05 | 0.00405961 | missense, stop-gained | GGA2 | GRCh38.p7 | 16:23493386 | ACACTTTGATCAGTT[A/C/G/T]GTTCAGGAAACGAAA | 23062 |
rs752865862 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23496066 | GCATTTTGGGAGGCC[A/G]AGGTGGGGGGAATCA | 23062 |
rs752867743 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23484522 | TAAGGAACCTGTATC[C/T]AGAATATATAAAAAA | 23062 |
rs752872531 | in-del | -/AAA | 0.000240918 | 0.0109727 | intron-variant | GGA2 | GRCh38.p7 | 16:23474867 | AATAGATTCCCAGGG[-/AAA]AAAAAAAAAAGGTGG | 23062 |
rs752879361 | snp | C/G | 9.72526e-05 | 0.00697258 | intron-variant | GGA2 | GRCh38.p7 | 16:23478715 | AACCTGTCTCCCCCA[C/G]GTATCAGCCAGACAG | 23062 |
rs752882262 | snp | A/G | 1.72493e-05 | 0.00293672 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23467644 | CACTTCTCCTACTTC[A/G]CTGAAAGGCTGTCCA | 23062 |
rs752989795 | snp | C/T | 6.62701e-05 | 0.00575593 | missense | GGA2 | GRCh38.p7 | 16:23482976 | CGGAACAGCGTGGGC[C/T]GCAGCTTTTCACACC | 23062 |
rs753060591 | snp | A/G | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504471 | GCTAGACAGTGTTTG[A/G]CCAGCTGGCTGGACA | 23062 |
rs753062374 | snp | A/G | 1.76229e-05 | 0.00296835 | intron-variant | GGA2 | GRCh38.p7 | 16:23470180 | CCTGGTATAAAGGGC[A/G]CAAGCAGAAGGTTTA | 23062 |
rs753079576 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23473736 | TTATAAAAAGTTATA[A/C]AACTAATACAAAAAT | 23062 |
rs753174621 | in-del | -/A | | | intron-variant | GGA2 | GRCh38.p7 | 16:23489801 | CCTGAAGGCGGGATT[-/A]GGGGGAGAAGAGTAA | 23062 |
rs753218368 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23505220 | CCTACTCATCACCTG[A/G]GAGTAGGACCAAGTG | 23062 |
rs753258269 | snp | A/G | 2.13956e-05 | 0.00327068 | intron-variant | GGA2 | GRCh38.p7 | 16:23479081 | GACTAATATGCAAGG[A/G]GGACCCTCTGAACTG | 23062 |
rs753351839 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23470208 | TTAACACCACTACAA[A/C]CCCCCCGGACAGCCA | 23062 |
rs753367548 | snp | C/T | 3.29457e-05 | 0.00405854 | intron-variant | GGA2 | GRCh38.p7 | 16:23488578 | GAGAAAAGGTCTGAT[C/T]AGACACCATGTAGGT | 23062 |
rs753379075 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23492191 | TTCAAGAGACACACT[C/T]GCAGGGTGCACCTGA | 23062 |
rs753390813 | in-del | -/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23471444 | AATACTCAGATAAAA[-/T]TACAATTCAAGTAAA | 23062 |
rs753464862 | snp | A/G | 1.6557e-05 | 0.00287719 | intron-variant | GGA2 | GRCh38.p7 | 16:23494396 | ACAGGGAAACAAAAA[A/G]ACCTAGACTCTGGGC | 23062 |
rs753484122 | snp | C/G | 3.61827e-05 | 0.00425324 | missense | GGA2 | GRCh38.p7 | 16:23467619 | AGACAGCCAGGTCTG[C/G]GAAGTCTTTCACTTC | 23062 |
rs753498161 | snp | C/T | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466264 | GACTTCAAAGCCCTC[C/T]GCCTAGCCATCTCAG | 23062 |
rs753561121 | snp | G/T | 1.64898e-05 | 0.00287135 | missense, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23494331 | AGAGCTTCCTTCTCT[G/T]GCGGAGACTGGATCT | 23062 |
rs753567180 | in-del | -/TC | | | intron-variant | GGA2 | GRCh38.p7 | 16:23507622 | AAGAATGAAACTCCA[-/TC]TCTCTCTCTCTCTCT | 23062 |
rs753569684 | snp | A/G/T | 3.29464e-05 | 0.00405861 | missense, synonymous-codon | GGA2 | GRCh38.p7 | 16:23486761 | CTGAAGGTCCTCGGG[A/G/T]TGGTTGCTCTTTAGA | 23062 |
rs753593323 | snp | C/T | 1.66776e-05 | 0.00288765 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23478451 | ACCACCGCCTGGCAG[C/T]GTGCTGGAGGAGGGA | 23062 |
rs753668109 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23506153 | GCTGCCTTGTTTGCA[A/G]GGACCTGATCTTGGC | 23062 |
rs753679982 | snp | C/T | 6.93842e-05 | 0.00588959 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465383 | CATAAACCACAGCCA[C/T]TTTCAGGACAGCAGC | 23062 |
rs753737355 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23487478 | TCTCTGGCCCAAAAG[A/G]GGACTAGGTCTGCAG | 23062 |
rs753776224 | snp | G/T | 1.66674e-05 | 0.00288676 | intron-variant | GGA2 | GRCh38.p7 | 16:23486201 | AGCAGAAACCCTGGC[G/T]GAAGCCTGAACAAGG | 23062 |
rs753860820 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23507900 | GAGAGGGGTAAGCTG[C/T]AGTGAGCTGAGATCA | 23062 |
rs753892594 | snp | C/T | | | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463533 | TCTTAAAAAAGACGA[C/T]ACTGAGCATAAAAAA | 23062 |
rs753917578 | snp | C/G/T | 7.18899e-05 | 0.00599504 | intron-variant | GGA2 | GRCh38.p7 | 16:23478824 | GGCAGTGCTGCCTCA[C/G/T]AAGGGCAGGTCTGAG | 23062 |
rs753919942 | snp | A/G | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503669 | AATGTTGTGTAAAAT[A/G]CTTCGTGCCCTGCAC | 23062 |
rs753924908 | snp | C/T | 2.0003e-05 | 0.00316245 | intron-variant | GGA2 | GRCh38.p7 | 16:23467752 | AGAGCAACCCAGGAA[C/T]AGGGGTCAATGTTAA | 23062 |
rs753938257 | snp | C/G | 0.000230867 | 0.0107415 | utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23510427 | CGCTCCAGCCCCGAC[C/G]CTGCGGCCGCGGGCG | 23062 |
rs753966165 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23494480 | CTTCCAGGGGCTGGT[A/G]TCCAAAAGCAGAGGT | 23062 |
rs754000598 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23506819 | ACGAACTTGTTTGCA[C/T]GTGCAATCATCTTGA | 23062 |
rs754017225 | snp | G/T | 0.000140105 | 0.00836857 | intron-variant | GGA2 | GRCh38.p7 | 16:23478747 | ATGGGTGAGGAAGAG[G/T]CTTTGGACCTCCAAG | 23062 |
rs754024013 | snp | A/G | 1.65982e-05 | 0.00288077 | missense | GGA2 | GRCh38.p7 | 16:23468974 | TTGGAGCTGGATGCC[A/G]GCTGCAGCTTCACTC | 23062 |
rs754130243 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23495873 | GCTGTCTTATCACAG[A/G]TCTACAGGATCAGAC | 23062 |
rs754177905 | snp | C/G | 3.68141e-05 | 0.00429019 | intron-variant | GGA2 | GRCh38.p7 | 16:23493495 | AGGAGAAGGTGGAAA[C/G]CCAGTGGTCCCAGGC | 23062 |
rs754219820 | snp | A/C/T | 8.41537e-05 | 0.00648619 | intron-variant | GGA2 | GRCh38.p7 | 16:23485975 | ATTTCAAACCCACTT[A/C/T]AGTAAACATGTGCAG | 23062 |
rs754366026 | snp | C/T | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503203 | CCCACTGTCGATTTG[C/T]GATTTCCTCCTCCAA | 23062 |
rs754373988 | snp | C/T | 1.64814e-05 | 0.00287061 | missense | GGA2 | GRCh38.p7 | 16:23493397 | AGTTCGTTCAGGAAA[C/T]GAAATTTGGCCACCT | 23062 |
rs754376769 | snp | G/T | 1.64993e-05 | 0.00287218 | intron-variant | GGA2 | GRCh38.p7 | 16:23474895 | GGTGGGGAGTGAAAT[G/T]GTACTTACTGGGCTT | 23062 |
rs754469385 | snp | C/T | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465560 | ATAAGTCTCATTCAC[C/T]CATTTTGACCAAAAC | 23062 |
rs754515984 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23492326 | CCTGACCGGTGCCCC[C/T]ACATCCCCCCACCTG | 23062 |
rs754527390 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23486093 | CAGCACCTTCACATG[A/G]CTTCGCACTTCCTCC | 23062 |
rs754559238 | snp | A/C | 2.30806e-05 | 0.00339702 | intron-variant | GGA2 | GRCh38.p7 | 16:23493515 | TGGTCCCAGGCTCCC[A/C]TCCAGGCTGGTAATC | 23062 |
rs754563115 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23498149 | GCTGGGCGTGGCAGC[A/G]TGCATCTATAATCCC | 23062 |
rs754586811 | snp | A/G | 7.35321e-05 | 0.00606306 | intron-variant | GGA2 | GRCh38.p7 | 16:23478777 | GGCCATGATCCCACC[A/G]GGACAGTGCAGGAGC | 23062 |
rs754661496 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23492949 | TTGTGGGAACACAAC[A/C]AGGCAGGGCTCAATG | 23062 |
rs754675878 | in-del | -/CT | 3.34429e-05 | 0.00408905 | intron-variant | GGA2 | GRCh38.p7 | 16:23485995 | AACATGTGCAGCCCC[-/CT]GTGTTACACCTGTAT | 23062 |
rs754698307 | snp | A/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466289 | TCTCAGCCAGGCTCA[A/G]GTTCCTTCTCCCACC | 23062 |
rs754721982 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23486240 | AGAGTCACTATTGAG[A/C]GAGCTCGCTCAGGGG | 23062 |
rs754741394 | snp | G/T | 0.000169047 | 0.00919212 | intron-variant | GGA2 | GRCh38.p7 | 16:23493590 | GCCTATGAGGACACT[G/T]AAGTTTTGATGAAGA | 23062 |
rs754772934 | snp | A/G | 1.73159e-05 | 0.00294239 | intron-variant | GGA2 | GRCh38.p7 | 16:23479928 | AAGTCAGTTGGACAT[A/G]AGAGCAAAGTCTCCA | 23062 |
rs754805524 | snp | A/G | 0.000181274 | 0.00951863 | missense | GGA2 | GRCh38.p7 | 16:23474925 | TAACAGACTCCAAAG[A/G]GACAAACACTTGAGC | 23062 |
rs754859869 | in-del | -/AAAAAAAAAAAAAAAAA | | | intron-variant | GGA2 | GRCh38.p7 | 16:23496309 | ACTCTGTCTCAAAAA[-/AAAAAAAAAAAAAAAAA]AAATTAACTGACAAG | 23062 |
rs754875432 | snp | A/G | 3.29451e-05 | 0.00405851 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23488636 | ATCAGCATCAAAGAT[A/G]GAGCTCTTGGGCCAG | 23062 |
rs754883358 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23474173 | AGCCAAATTCATCCA[C/G]TCGTTTGAATTCTAC | 23062 |
rs754908936 | snp | C/G | 3.80452e-05 | 0.00436133 | intron-variant | GGA2 | GRCh38.p7 | 16:23467738 | TGTCAAATCAGTGGA[C/G]AGCAACCCAGGAACA | 23062 |
rs754939114 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23475648 | GTGGCTCACGCCTGT[A/G]ATCCCAGCATTTTGG | 23062 |
rs754964377 | snp | A/C | 3.30322e-05 | 0.00406387 | missense | GGA2 | GRCh38.p7 | 16:23479834 | CAGGTCCATTGTCCA[A/C]CTCCAAGTCAATCAG | 23062 |
rs755009535 | snp | A/G | 3.37798e-05 | 0.00410959 | intron-variant | GGA2 | GRCh38.p7 | 16:23478512 | GAAACCTGTCAAATC[A/G]GGAATGGCTAAAATA | 23062 |
rs755037170 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23495954 | CCACCCAGCACAGCA[C/T]TGGGCACATGGTATG | 23062 |
rs755063230 | snp | A/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23482438 | CCCCTCTCTCATGTT[A/T]CGAGATTTTCCACAA | 23062 |
rs755116658 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23494559 | CTCGCACCCACCCTG[A/G]TTGCACCTACAGCAC | 23062 |
rs755212469 | snp | A/G | 1.6507e-05 | 0.00287284 | intron-variant | GGA2 | GRCh38.p7 | 16:23480776 | AGAATTTCCGCTGAA[A/G]AATGAGGGAAGACTC | 23062 |
rs755214513 | snp | C/T | 0.000165615 | 0.00909836 | intron-variant | GGA2 | GRCh38.p7 | 16:23493313 | CCAGGAGTTTGACAG[C/T]GGGCGTAGGTGCGAC | 23062 |
rs755302527 | snp | A/T | 1.65529e-05 | 0.00287683 | missense | GGA2 | GRCh38.p7 | 16:23482930 | AAACTTACCGAGTGC[A/T]TCATCGTCATCAGTG | 23062 |
rs755330227 | snp | A/G | 1.6759e-05 | 0.00289469 | missense | GGA2 | GRCh38.p7 | 16:23470039 | TCCCAGACAGGCTGG[A/G]GAGCCGTGCTCATCA | 23062 |
rs755338432 | snp | C/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23502333 | CATCTTACCCCAGGC[C/T]GATAATGGTCATGCC | 23062 |
rs755363232 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23470687 | AAAATCACTTGAACT[C/T]GGGAGGCGGAGGTTG | 23062 |
rs755375146 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23486439 | CTTTGTCCATACCAA[C/T]ACCTGTTGCTGGGAC | 23062 |
rs755410939 | snp | A/C | 3.29451e-05 | 0.00405851 | missense | GGA2 | GRCh38.p7 | 16:23491738 | CGGAAACCAGACTGT[A/C]CAACTGAAGAGTATT | 23062 |
rs755436439 | snp | A/C | 1.67114e-05 | 0.00289057 | intron-variant | GGA2 | GRCh38.p7 | 16:23478869 | TCTCCGGGCCCTGGG[A/C]AGGGCATCCTTACCA | 23062 |
rs755487746 | snp | A/G | 5.94183e-05 | 0.00545029 | intron-variant | GGA2 | GRCh38.p7 | 16:23478967 | CACCTGCTTCCAGAT[A/G]AAGAGTAATGCCACA | 23062 |
rs755491151 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23490614 | GTGGCAGGTGCCTGT[A/G]ATCCCAGCTACTCGA | 23062 |
rs755527794 | snp | A/T | 1.69372e-05 | 0.00291004 | intron-variant | GGA2 | GRCh38.p7 | 16:23469028 | ACCAACATGTAACTC[A/T]TTCCTAACCACAGCT | 23062 |
rs755650798 | snp | C/T | 4.3572e-05 | 0.00466735 | intron-variant | GGA2 | GRCh38.p7 | 16:23478981 | TGAAGAGTAATGCCA[C/T]ACCCATCCTTTCTAG | 23062 |
rs755712341 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23489240 | GCAAATTCACAATAT[G/T]TTTGTTGTTTTTGAG | 23062 |
rs755748483 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23508570 | CCTTTGCTATCAGTG[A/G]GTGCCCCTGCAGGTC | 23062 |
rs755795228 | snp | A/T | 1.64868e-05 | 0.00287109 | missense, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23494325 | GCATAAAGAGCTTCC[A/T]TCTCTTGCGGAGACT | 23062 |
rs755849463 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23498042 | CCTAGCACTTTGGGA[A/G]GCCGAGGAGGGTGGA | 23062 |
rs755887692 | snp | C/G | 1.6477e-05 | 0.00287024 | intron-variant | GGA2 | GRCh38.p7 | 16:23486663 | TGCACTGTCCTTCAG[C/G]CTCTGTCAAATGCTA | 23062 |
rs755894494 | snp | C/T | 0.000108021 | 0.00734837 | intron-variant | GGA2 | GRCh38.p7 | 16:23478337 | CACTCAGGAGCCACA[C/T]TCTCCCACTCCCCTT | 23062 |
rs755904380 | snp | A/G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23496525 | AATACCATCTTGACC[A/G/T]TTCATAAAACTTCCA | 23062 |
rs755911875 | snp | A/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466007 | TAAAATTCGTCTTAT[A/G]TGAATTATGGCAAAT | 23062 |
rs755941124 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23472094 | ATTTCACTGGTATTA[C/T]GATCTCCTCATAATC | 23062 |
rs755970848 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23484844 | GTTACCCCAAGATCC[A/G]GCAATTCCATTTCTA | 23062 |
rs755991968 | snp | A/C | 6.21214e-05 | 0.00557287 | intron-variant | GGA2 | GRCh38.p7 | 16:23493608 | GTTTTGATGAAGAGG[A/C]CGTTTTCAGATCAAG | 23062 |
rs756013980 | snp | C/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500693 | TGTGGCGGGTGGAAC[C/T]GCCCTGCAGCTATAA | 23062 |
rs756016480 | snp | G/T | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465323 | AAGAGGTAGGAGCTG[G/T]GCTCTAAGTGGCCAC | 23062 |
rs756060519 | snp | A/C | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503534 | TGATAGTTGAAAATA[A/C]ATGGCAAAATAAGAA | 23062 |
rs756089549 | snp | C/T | 3.45161e-05 | 0.00415414 | splice-acceptor-variant | GGA2 | GRCh38.p7 | 16:23475062 | TGCGAAACATAATTC[C/T]TACAAAGAAATAAAA | 23062 |
rs756090953 | snp | C/T | 1.64866e-05 | 0.00287106 | missense | GGA2 | GRCh38.p7 | 16:23480753 | GGGTGAGGAGGTCAT[C/T]TGCCTGGAGAATTTC | 23062 |
rs756165727 | snp | A/C | 5.58238e-05 | 0.00528288 | intron-variant | GGA2 | GRCh38.p7 | 16:23495810 | AAAGTTAGAGAGTAC[A/C]TAATAGGAAGAAATT | 23062 |
rs756211802 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23506687 | AGAAACCCAGCTCTC[C/T]GTCCGGGTGGGCCCA | 23062 |
rs756239679 | in-del | -/TGAA | 0.000163787 | 0.00904801 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465302 | TAACTACTTGTTAAG[-/TGAA]TGAAGAGGTAGGAGC | 23062 |
rs756248372 | in-del | -/TT | | | intron-variant | GGA2 | GRCh38.p7 | 16:23472187 | TTTGTAGCCCTGGTT[-/TT]TTTTTTTTTTTTTTT | 23062 |
rs756256475 | snp | C/G | 1.6764e-05 | 0.00289512 | intron-variant | GGA2 | GRCh38.p7 | 16:23478735 | CAGCCAGACAGTATG[C/G]GTGAGGAAGAGGCTT | 23062 |
rs756260632 | snp | A/C | 1.71749e-05 | 0.00293038 | missense | GGA2 | GRCh38.p7 | 16:23467648 | TCTCCTACTTCGCTG[A/C]AAGGCTGTCCACCTT | 23062 |
rs756266829 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23505531 | ACCACAGAACTGAAT[C/G]ACAGAATGCACAGGC | 23062 |
rs756316108 | snp | C/T | 1.66134e-05 | 0.00288208 | missense | GGA2 | GRCh38.p7 | 16:23482988 | GGCCGCAGCTTTTCA[C/T]ACCTCTCATACACGA | 23062 |
rs756324472 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23481437 | ATGCCACGAGCAAAA[C/G]TGAGACCGAGAGAAC | 23062 |
rs756371068 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23494260 | TCGGCTCTCTATAGC[A/C]CAAGGACAGGAAAGG | 23062 |
rs756380219 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23469649 | AATATATGTGCTTCA[C/T]GCCCGGTGAGAGTTT | 23062 |
rs756428895 | snp | C/G | 1.72291e-05 | 0.002935 | intron-variant | GGA2 | GRCh38.p7 | 16:23495673 | CCCAGAGTCAACTAT[C/G]TGTGTGAGAAGTTAC | 23062 |
rs756447749 | snp | C/T | 0.000330677 | 0.0128541 | missense | GGA2 | GRCh38.p7 | 16:23482940 | AGTGCATCATCGTCA[C/T]CAGTGGTGTCACTCG | 23062 |
rs756450753 | snp | C/G | 1.66062e-05 | 0.00288146 | intron-variant | GGA2 | GRCh38.p7 | 16:23478625 | CTGGTGACATCTCTT[C/G]GGGCAAGAGGGGAAA | 23062 |
rs756490528 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23482312 | TTTGCTTCAAAACAG[A/G]CTAGGGAATGGGTGT | 23062 |
rs756527346 | snp | A/G | 2.13883e-05 | 0.00327012 | intron-variant | GGA2 | GRCh38.p7 | 16:23479082 | ACTAATATGCAAGGG[A/G]GACCCTCTGAACTGC | 23062 |
rs756587152 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23509983 | GGGAATGAGGATTAA[A/G]CAGGACTAAGCCGCT | 23062 |
rs756592274 | snp | A/G | 0.000199973 | 0.00999733 | missense | GGA2 | GRCh38.p7 | 16:23470045 | ACAGGCTGGGGAGCC[A/G]TGCTCATCATGGTCA | 23062 |
rs756641478 | snp | A/G | 3.31181e-05 | 0.00406914 | intron-variant | GGA2 | GRCh38.p7 | 16:23493318 | AGTTTGACAGTGGGC[A/G]TAGGTGCGACACAGT | 23062 |
rs756662511 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23470533 | TTTAGGAGGCCAAGG[C/T]GGGTGGATCACTTGA | 23062 |
rs756775734 | snp | C/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501663 | TGCACTAATGCCATC[C/T]TAAAGAGAGAAATTA | 23062 |
rs756826676 | snp | A/C/T | 0.000184973 | 0.00961549 | intron-variant | GGA2 | GRCh38.p7 | 16:23470214 | CCACTACAAACCCCC[A/C/T]GGACAGCCAGGCTGG | 23062 |
rs756826817 | snp | A/C | 3.30093e-05 | 0.00406246 | missense | GGA2 | GRCh38.p7 | 16:23479801 | GAAGCAAAGATGGCA[A/C]CACAGTCCCCATCTG | 23062 |
rs756829201 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23476034 | TCATGTTGTACCTGT[C/T]GGGCAGTCCCTGACA | 23062 |
rs756876617 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23468112 | TGACTTTCTTTTCTT[C/T]TTCTCTTCTCCTTCC | 23062 |
rs756903322 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23471886 | CGCACTCCTGCCTAG[A/G]CGATGGAGCGAGGCC | 23062 |
rs756933225 | snp | A/G | 2.87171e-05 | 0.00378916 | intron-variant | GGA2 | GRCh38.p7 | 16:23479009 | TAGGACATCCAGAAA[A/G]TCTAGACAAATAAGC | 23062 |
rs757009511 | snp | A/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500126 | AAGGAAACCAAACAG[A/G]TTCCCAAGGGACCCT | 23062 |
rs757015608 | snp | C/T | 1.65726e-05 | 0.00287855 | intron-variant | GGA2 | GRCh38.p7 | 16:23494400 | GGAAACAAAAAGACC[C/T]AGACTCTGGGCGGGC | 23062 |
rs757020670 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463882 | TGAAGCCGGAGGATC[A/G]CCTGAACACAGGAAT | 23062 |
rs757022814 | snp | C/T | 0.000199134 | 0.00997633 | intron-variant | GGA2 | GRCh38.p7 | 16:23479722 | GCTCACTCCCCTACT[C/T]GCACCCATCCTGTGC | 23062 |
rs757030315 | snp | A/G | 0.000161721 | 0.00899078 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465439 | CCTGTCCAACACCTA[A/G]GCATAGTAGTACCAC | 23062 |
rs757090518 | snp | C/T | 1.64754e-05 | 0.00287009 | intron-variant | GGA2 | GRCh38.p7 | 16:23486685 | CAAATGCTACTTCTA[C/T]TGAACCAACTGGAAG | 23062 |
rs757131496 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23477436 | CTCTCATTCTCTCGT[C/T]TGCTGCCACATAAGA | 23062 |
rs757292595 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23474063 | TAGAGACGGTAGGCA[A/C]CTTAATTAGCCGAGC | 23062 |
rs757297346 | snp | A/G | 1.6869e-05 | 0.00290417 | intron-variant | GGA2 | GRCh38.p7 | 16:23488754 | CCGATATGGTACCCA[A/G]AAACTTCAGTCAGAA | 23062 |
rs757381237 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23486180 | AGAGGAGGATGGGAG[G/T]GAGGGAGCAGAAACC | 23062 |
rs757394655 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23505423 | AGGACACCCATACAA[C/T]GGGGCGTCTAAGGCT | 23062 |
rs757456207 | snp | C/T | 1.65902e-05 | 0.00288008 | intron-variant | GGA2 | GRCh38.p7 | 16:23478749 | GGGTGAGGAAGAGGC[C/T]TTGGACCTCCAAGGC | 23062 |
rs757478621 | snp | C/T | 2.15404e-05 | 0.00328172 | intron-variant | GGA2 | GRCh38.p7 | 16:23495828 | ATAGGAAGAAATTTA[C/T]ACCCCTCCCCATACA | 23062 |
rs757478688 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23492631 | ACCTTGCCTATGTAT[C/T]GCTTCCATTTGTATC | 23062 |
rs757492980 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23480533 | AGGGGAACAAAGGGC[A/G]AGTTCTCTCATTTCT | 23062 |
rs757590565 | snp | A/G | 1.67167e-05 | 0.00289103 | intron-variant | GGA2 | GRCh38.p7 | 16:23468846 | CCCCTTACAGTTCAG[A/G]GGCCCCCATCTCCCT | 23062 |
rs757628244 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23493131 | TCCTCTAGGCCACAC[A/G]TTCCCCAGGCCTTCT | 23062 |
rs757689402 | in-del | -/CTTAA | 1.64855e-05 | 0.00287097 | frameshift-variant | GGA2 | GRCh38.p7 | 16:23474908 | ATTGTACTTACTGGG[-/CTTAA]CAGACTCCAAAGGGA | 23062 |
rs757783104 | snp | C/T | 1.64928e-05 | 0.00287161 | intron-variant | GGA2 | GRCh38.p7 | 16:23474901 | GAGTGAAATTGTACT[C/T]ACTGGGCTTAACAGA | 23062 |
rs757783939 | in-del | -/A | 1.71968e-05 | 0.00293225 | frameshift-variant | GGA2 | GRCh38.p7 | 16:23467681 | TGAATGTCAGCTTGT[-/A]ACCGTAAGCGGATAG | 23062 |
rs757786346 | snp | A/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467479 | CACCCAGAGCCTGAC[A/G]TCAGGATAGGACTCT | 23062 |
rs757790380 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23482142 | GATGGTGGGTGCCTA[C/T]AATCCCAGCTACTTG | 23062 |
rs757807277 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23475636 | AGGCTGGGCACGGTG[C/G]CTCACGCCTGTAATC | 23062 |
rs757821082 | snp | A/G | 5.88841e-05 | 0.00542574 | intron-variant | GGA2 | GRCh38.p7 | 16:23493502 | GGTGGAAAGCCAGTG[A/G]TCCCAGGCTCCCCTC | 23062 |
rs757977075 | snp | C/T | 1.64836e-05 | 0.0028708 | missense | GGA2 | GRCh38.p7 | 16:23474985 | GAGCCAACGGGCCAG[C/T]CTCCCAGGACCAACC | 23062 |
rs758000058 | snp | A/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23496295 | GAGACAGAGGGAGAC[A/T]CTGTCTCAAAAAAAA | 23062 |
rs758050163 | in-del | -/GT | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510871 | ACCACCACGCCTGGC[-/GT]GTGTGTGTGTGTGTG | 23062 |
rs758060139 | in-del | -/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23474362 | GACAAAGAAGCAAAC[-/T]TTTTTTTTTTTTGGA | 23062 |
rs758105692 | snp | A/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500820 | CATCAGTGACCAGGA[A/G]ATGCCCAAATATTTT | 23062 |
rs758135142 | snp | C/T | 4.94173e-05 | 0.00497053 | intron-variant | GGA2 | GRCh38.p7 | 16:23488602 | TGTAGGTCTGTTTCC[C/T]TACCTTGGACTTTTC | 23062 |
rs758210704 | snp | A/G | 0.000160754 | 0.00896387 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467546 | CTAGACAGCAAAAGT[A/G]ACGCCAGCCTAAGCT | 23062 |
rs758219051 | snp | C/G | 1.65759e-05 | 0.00287883 | intron-variant | GGA2 | GRCh38.p7 | 16:23479726 | ACTCCCCTACTCGCA[C/G]CCATCCTGTGCCTGC | 23062 |
rs758255539 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23506842 | CATCTTGATCTCCTT[C/T]GCCAGACAGTCAGAA | 23062 |
rs758280565 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23487817 | GAGTATCTAGGCCCA[A/C]GGAGTGGGTACAGGG | 23062 |
rs758298687 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23477233 | CTGGGATTACAGGTA[C/T]GATATGGTTTGGCTG | 23062 |
rs758303693 | snp | A/T | 1.75965e-05 | 0.00296613 | intron-variant | GGA2 | GRCh38.p7 | 16:23495645 | CAAAGGCCTACACTC[A/T]GTGTGGGGTGCCCCC | 23062 |
rs758401729 | snp | A/G | 1.73534e-05 | 0.00294558 | missense | GGA2 | GRCh38.p7 | 16:23467639 | TCTTTCACTTCTCCT[A/G]CTTCGCTGAAAGGCT | 23062 |
rs758401937 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23505585 | ATGAGATTCTGGTAA[C/T]GGCTTCCTGATACTC | 23062 |
rs758415721 | snp | A/C/T | 6.59929e-05 | 0.00574393 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23480769 | TGCCTGGAGAATTTC[A/C/T]GCTGAAGAATGAGGG | 23062 |
rs758424028 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23486779 | GTTGCTCTTTAGAAG[C/T]CTTGTCAGAAGCTGC | 23062 |
rs758444654 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23484554 | GCTTGTAACTCAAAA[A/C]AGACAATCCAAAAGA | 23062 |
rs758474905 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23483365 | TACAAAAGTTAGTGG[C/G]TGCCTGTAATCCCAG | 23062 |
rs758513321 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23509618 | ATTGGTAAAACGGAG[A/G]TAATAATAACCCCTA | 23062 |
rs758590159 | snp | C/T | 3.35683e-05 | 0.00409671 | intron-variant | GGA2 | GRCh38.p7 | 16:23469014 | ATCAGGGGAAGAAAA[C/T]CAACATGTAACTCAT | 23062 |
rs758637178 | snp | A/C | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503557 | AATAAGAATTGCTGA[A/C]ACCTAGTGATAATGT | 23062 |
rs758665279 | snp | C/T | 1.64906e-05 | 0.00287142 | intron-variant | GGA2 | GRCh38.p7 | 16:23491636 | GCAAGAAGATACAGG[C/T]CTAGTCAAGAGGAAA | 23062 |
rs758673521 | in-del | -/AAAAAA | | | intron-variant | GGA2 | GRCh38.p7 | 16:23495079 | ACACTCTGTCTCAGG[-/AAAAAA]AAAAAAAGAAAAGAA | 23062 |
rs758682994 | snp | C/T | 1.66615e-05 | 0.00288626 | intron-variant | GGA2 | GRCh38.p7 | 16:23468856 | TTCAGGGGCCCCCAT[C/T]TCCCTGCTACCACAG | 23062 |
rs758697070 | snp | C/G | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504475 | GACAGTGTTTGGCCA[C/G]CTGGCTGGACATACT | 23062 |
rs758715738 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23492503 | AAACCTCAGATGAAA[A/C]CACTGAAACAAGGAA | 23062 |
rs758751355 | snp | A/G | 3.29457e-05 | 0.00405854 | missense | GGA2 | GRCh38.p7 | 16:23491724 | ATCTTGATGTCTTCC[A/G]GAAACCAGACTGTCC | 23062 |
rs758758667 | snp | C/T | 1.73219e-05 | 0.0029429 | intron-variant | GGA2 | GRCh38.p7 | 16:23478835 | CTCACAAGGGCAGGT[C/T]TGAGACCCTCCCATT | 23062 |
rs758819679 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23489811 | GGATTAGGGGGAGAA[A/G]AGTAACAAACCCTGC | 23062 |
rs758867208 | snp | C/T | 1.67899e-05 | 0.00289736 | intron-variant | GGA2 | GRCh38.p7 | 16:23485986 | ACTTTAGTAAACATG[C/T]GCAGCCCCCTGTGTT | 23062 |
rs758871543 | snp | A/C/T | 0.000132048 | 0.00812458 | missense | GGA2 | GRCh38.p7 | 16:23479785 | GCTGCCAGGTCCTGA[A/C/T]GAAGCAAAGATGGCA | 23062 |
rs758882182 | in-del | -/A | 1.74665e-05 | 0.00295515 | intron-variant | GGA2 | GRCh38.p7 | 16:23478699 | GCAGGAGCCTGGTGC[-/A]AACCTGTCTCCCCCA | 23062 |
rs758949392 | snp | A/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23487308 | CAGTGGGGTAGGGGG[A/T]TGTGGGGGTTACTTC | 23062 |
rs758950568 | in-del | -/A | | | intron-variant | GGA2 | GRCh38.p7 | 16:23468773 | ACCACTGTGCCCAGC[-/A]AACCAGAGACTTTAG | 23062 |
rs758952030 | snp | A/G | 0.000116635 | 0.00763569 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23478415 | GTCCAGCAAATTCCT[A/G]TCTGCAGAAGGGTTC | 23062 |
rs758956955 | snp | A/G | 0.000102412 | 0.0071551 | intron-variant | GGA2 | GRCh38.p7 | 16:23478763 | CTTTGGACCTCCAAG[A/G]CCATGATCCCACCGG | 23062 |
rs758957059 | snp | C/G | 4.94295e-05 | 0.00497115 | missense | GGA2 | GRCh38.p7 | 16:23486064 | GGCCTGCGGTACATG[C/G]TCAGCATCTCCTGCA | 23062 |
rs759003577 | in-del | -/CAG | 1.64798e-05 | 0.00287047 | cds-indel | GGA2 | GRCh38.p7 | 16:23480724 | CATCACCTGTTTGTA[-/CAG]CAGAACTCCTTGGGT | 23062 |
rs759116799 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23505138 | GGAGGGACACGTGGA[C/T]CCCAAGAGTCCGGCA | 23062 |
rs759135198 | snp | A/G | 1.64811e-05 | 0.00287059 | missense | GGA2 | GRCh38.p7 | 16:23480740 | AGCAGAACTCCTTGG[A/G]TGAGGAGGTCATTTG | 23062 |
rs759139238 | snp | C/G | 1.65002e-05 | 0.00287225 | missense | GGA2 | GRCh38.p7 | 16:23491790 | TTTCCTGTGGCCCAG[C/G]ACCCCAGGTACTGAA | 23062 |
rs759203908 | snp | A/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500580 | CATCTATGAGGCAGC[A/G]TCAAGCAAAGGTGCA | 23062 |
rs759218884 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23493803 | GGTATCCAGTGCCCA[A/G]GACCAGCCGGATGTC | 23062 |
rs759238529 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23468475 | GCCACTGCACCTGGC[C/T]GACTTTATTTTTTTT | 23062 |
rs759264998 | snp | A/G | | | stop-gained | GGA2 | GRCh38.p7 | 16:23480717 | GGCCCTCCATCACCT[A/G]TTTGTACAGCAGAAC | 23062 |
rs759270689 | snp | A/G | 1.80214e-05 | 0.00300173 | intron-variant | GGA2 | GRCh38.p7 | 16:23478323 | ATGAGAAGGAACCGC[A/G]CTCAGGAGCCACACT | 23062 |
rs759298207 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23481812 | TGCAGAGGGCATGCA[C/G]ATGCTATCCACTAAG | 23062 |
rs759477788 | in-del | -/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465716 | GAGGCCAAGGCAGGC[-/G]GATCACCTGAGGTCA | 23062 |
rs759483473 | snp | A/C | 0.00030216 | 0.0122878 | missense, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23510390 | TTCCCGCCACAGCCG[A/C]CGCCACCGCGGTCGC | 23062 |
rs759485260 | snp | A/C | 1.9365e-05 | 0.00311161 | intron-variant | GGA2 | GRCh38.p7 | 16:23478812 | CTCTGCTCGCCAGGC[A/C]GTGCTGCCTCACAAG | 23062 |
rs759487415 | snp | C/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501283 | TCTGTGTCCTACTAA[C/T]TGGAAAAAGATTGTC | 23062 |
rs759528872 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23479178 | TCACAACCACCCTGA[C/T]TGCCTCAGCAGCAGG | 23062 |
rs759580978 | snp | C/G | 3.38118e-05 | 0.00411154 | intron-variant | GGA2 | GRCh38.p7 | 16:23478928 | TGTAAGAAAGGAGTA[C/G]AGTGAGATGCCTAAC | 23062 |
rs759599210 | snp | A/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464997 | ACGGAGGTAGGTCAC[A/G]AAATGGGTCAACAGG | 23062 |
rs759614909 | snp | C/T | 3.30311e-05 | 0.0040638 | missense | GGA2 | GRCh38.p7 | 16:23479774 | CCTCACCCAAGGCTG[C/T]CAGGTCCTGATGAAG | 23062 |
rs759661428 | snp | A/C/T | 6.73849e-05 | 0.0058042 | intron-variant | GGA2 | GRCh38.p7 | 16:23493475 | TGCACAGACACAGGA[A/C/T]CCCCAGGAGAAGGTG | 23062 |
rs759691471 | snp | C/G/T | 0.000149001 | 0.00863031 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23482972 | CAACCGGAACAGCGT[C/G/T]GGCCGCAGCTTTTCA | 23062 |
rs759694967 | snp | A/G | 1.74193e-05 | 0.00295116 | intron-variant | GGA2 | GRCh38.p7 | 16:23470168 | GGCGGCAGGCTGCCT[A/G]GTATAAAGGGCACAA | 23062 |
rs759750321 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23492401 | TTCAACTATGTGGCC[A/G]ATGATTTGACCGATC | 23062 |
rs759760395 | snp | A/C | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465852 | AGGCTGAGGCACGAG[A/C]ATCGCTTGAACCTGG | 23062 |
rs759777159 | snp | C/G | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23512018 | AAAGACAAAGAAAGG[C/G]TAGAACCTGGAAGGT | 23062 |
rs759814759 | snp | C/T | 1.6476e-05 | 0.00287014 | intron-variant | GGA2 | GRCh38.p7 | 16:23486829 | TAGGTGAGACCACAA[C/T]TCCCTCAGGCCTAGA | 23062 |
rs759914828 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23485721 | ACGTGAATGGATCTC[A/G]AGTGAGATCCAGAAA | 23062 |
rs759940696 | snp | A/G | 6.17316e-05 | 0.00555536 | intron-variant | GGA2 | GRCh38.p7 | 16:23479075 | ATCTGTGACTAATAT[A/G]CAAGGGGGACCCTCT | 23062 |
rs760006255 | snp | G/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499018 | GGAAGAGAACAGGGG[G/T]AGGCAGGGAGAGAAC | 23062 |
rs760024771 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23474163 | GAGGATCACTAGCCA[A/G]ATTCATCCACTCGTT | 23062 |
rs760035615 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23484444 | CAAAACAAAACTCCC[A/G]CTTCAAAAGATGCTA | 23062 |
rs760076518 | snp | A/G | 1.6517e-05 | 0.00287372 | missense, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23494373 | AGCCAGGGCGCATGT[A/G]TGGGGCTACAGGGAA | 23062 |
rs760106544 | snp | C/T | 1.99074e-05 | 0.00315489 | missense | GGA2 | GRCh38.p7 | 16:23467600 | AAAAGTTAGGCTGCG[C/T]CCAAGACAGCCAGGT | 23062 |
rs760133186 | snp | A/G | 1.6473e-05 | 0.00286988 | stop-gained | GGA2 | GRCh38.p7 | 16:23486748 | ACCGGTTTGCAGCCT[A/G]AAGGTCCTCGGGGTG | 23062 |
rs760141884 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23473436 | CTGCCATCTGGGTTC[A/C]GGTGATTCTCCAGGC | 23062 |
rs760154612 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23471872 | TATGACTGTGCCACC[A/G]CACTCCTGCCTAGGC | 23062 |
rs760229263 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23473242 | ATGTACATATATATG[C/T]ATATGATAAGACAAG | 23062 |
rs760236558 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23482177 | GCTGAGGAAGGAGAA[C/T]GGCTTGAACCAGGGA | 23062 |
rs760267372 | snp | C/T | 3.33267e-05 | 0.00408194 | missense | GGA2 | GRCh38.p7 | 16:23478441 | GGTTCTGAACACCAC[C/T]GCCTGGCAGCGTGCT | 23062 |
rs760321001 | snp | A/G | 6.61387e-05 | 0.00575021 | missense | GGA2 | GRCh38.p7 | 16:23482962 | TGTCACTCGCCAACC[A/G]GAACAGCGTGGGCCG | 23062 |
rs760326241 | in-del | -/A | | | intron-variant | GGA2 | GRCh38.p7 | 16:23470933 | TCCCGGATTCAAACG[-/A]ATTCTCCCACCTCAG | 23062 |
rs760336438 | snp | A/G | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23512140 | GGAAGAAGAGACCCA[A/G]AGCCACTGAATGAGG | 23062 |
rs760347388 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23492006 | TCGGCAATACTCACA[C/T]TAAACCCCACCATGC | 23062 |
rs760353474 | snp | C/G | 1.77181e-05 | 0.00297636 | intron-variant | GGA2 | GRCh38.p7 | 16:23478556 | AATGACCATCAGCCA[C/G]AGTAAAACCAAGGCA | 23062 |
rs760448654 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23492871 | GGGGTCCGGGTAGCA[C/T]GCAACTCAGGGGAGT | 23062 |
rs760461663 | snp | A/C | 1.66724e-05 | 0.0028872 | intron-variant | GGA2 | GRCh38.p7 | 16:23482904 | GGCTGCTAGCTACAC[A/C]CAAGGAAAGAAAACT | 23062 |
rs760462361 | snp | A/G | 1.65356e-05 | 0.00287533 | intron-variant | GGA2 | GRCh38.p7 | 16:23494387 | TGTGGGGCTACAGGG[A/G]AACAAAAAGACCTAG | 23062 |
rs760483225 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23480530 | GGAAGGGGAACAAAG[A/G]GCGAGTTCTCTCATT | 23062 |
rs760515075 | snp | C/T | 1.64996e-05 | 0.0028722 | intron-variant | GGA2 | GRCh38.p7 | 16:23493348 | TCAGCAGAGCCAAGC[C/T]CAGGTACTCACCTTT | 23062 |
rs760553146 | snp | A/C | 1.67584e-05 | 0.00289464 | missense | GGA2 | GRCh38.p7 | 16:23470129 | AGCAGAATTCTGAAT[A/C]CATTCCGGTCATACA | 23062 |
rs760596835 | snp | A/G | 1.73616e-05 | 0.00294627 | missense | GGA2 | GRCh38.p7 | 16:23470009 | ACCTTTGGCACAGCC[A/G]CTTGAAACATGATAT | 23062 |
rs760607915 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23479635 | TGCTCCCAGAGGGAA[C/T]CAGCTCACTCTTCCT | 23062 |
rs760684269 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23477087 | CTCCTGAGCAGCTGG[G/T]ACTACAGTCATGACC | 23062 |
rs760722280 | snp | A/T | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467145 | CCCTTTTAAGGTCCC[A/T]GAGAACAGCAGCCTG | 23062 |
rs760746101 | snp | A/G | 1.648e-05 | 0.0028705 | missense | GGA2 | GRCh38.p7 | 16:23474966 | TTCTGTGAAGATGGG[A/G]AAGGAGCCAACGGGC | 23062 |
rs760802538 | snp | A/G | 1.64874e-05 | 0.00287113 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23486039 | CTCCTGGTCGGGCGG[A/G]GCCTGCCCTGGCCTG | 23062 |
rs760825505 | in-del | -/TGTAAG | | | intron-variant | GGA2 | GRCh38.p7 | 16:23480603 | TGGGAATTACAGGCT[-/TGTAAG]GCCCCAAGGCAGAGA | 23062 |
rs760836346 | snp | A/G | | | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463456 | TCTGAAAAGACAGAG[A/G]ATGGTAACTGGGTGG | 23062 |
rs760921343 | in-del | -/A | 0.113866 | 0.209684 | intron-variant | GGA2 | GRCh38.p7 | 16:23474866 | AATAGATTCCCAGGG[-/A]AAAAAAAAAAAAAGG | 23062 |
rs760936527 | snp | A/C | 1.67857e-05 | 0.00289699 | splice-acceptor-variant | GGA2 | GRCh38.p7 | 16:23479888 | CTGGATTCTGAAAGA[A/C]TAGAAAGCCCAGGGT | 23062 |
rs761005900 | snp | C/T | 0.000214321 | 0.0103496 | intron-variant | GGA2 | GRCh38.p7 | 16:23493546 | ACTTGCTGGAGACTG[C/T]GCTGGAACCAAGGCT | 23062 |
rs761046668 | snp | A/G | 1.89437e-05 | 0.00307758 | intron-variant | GGA2 | GRCh38.p7 | 16:23483054 | CAGGCACCCCATAAC[A/G]CCCCCCTCCAGGGCC | 23062 |
rs761091642 | snp | G/T | 0.000743218 | 0.0192628 | intron-variant | GGA2 | GRCh38.p7 | 16:23474889 | AAAAAAGGTGGGGAG[G/T]GAAATTGTACTTACT | 23062 |
rs761120970 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23484357 | CGGGAGGCAGAAGTC[A/G]TGCGGAGCTGAGATC | 23062 |
rs761177375 | snp | C/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501212 | AAAACTACAGCTCCA[C/T]GTGCAATCGTAGCTT | 23062 |
rs761190741 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23509089 | ACCCTCTCCGCCCAA[C/T]TTAGCACCATATGGC | 23062 |
rs761190932 | snp | C/T | 1.67829e-05 | 0.00289675 | synonymous-codon, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23495774 | GCTTGGGTCTGTGGC[C/T]TTGTCTGTCAAATAA | 23062 |
rs761217147 | snp | A/G | 1.64787e-05 | 0.00287038 | intron-variant | GGA2 | GRCh38.p7 | 16:23486842 | AACTCCCTCAGGCCT[A/G]GAGCAGAAGCAGCAG | 23062 |
rs761226256 | in-del | -/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23492627 | CAAGACCTTGCCTAT[-/G]TATCGCTTCCATTTG | 23062 |
rs761229140 | snp | C/T | 1.64776e-05 | 0.00287028 | missense | GGA2 | GRCh38.p7 | 16:23488695 | CTGGTAGTTTAGGGT[C/T]TTGTTTTATAATTCC | 23062 |
rs761387519 | snp | A/G | 1.80117e-05 | 0.00300092 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23467620 | GACAGCCAGGTCTGG[A/G]AAGTCTTTCACTTCT | 23062 |
rs761454511 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23505209 | CATGGGAATGTCCTA[C/T]TCATCACCTGGGAGT | 23062 |
rs761463518 | snp | C/T | 1.73963e-05 | 0.00294921 | intron-variant | GGA2 | GRCh38.p7 | 16:23478703 | GGAGCCTGGTGCAAC[C/T]TGTCTCCCCCAGGTA | 23062 |
rs761464461 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23471770 | AATTTGCTGGGTGTG[C/G]TGGTGCATGCCTGTC | 23062 |
rs761476497 | snp | C/T | 0.000122037 | 0.00781049 | missense | GGA2 | GRCh38.p7 | 16:23467694 | TGTACCGTAAGCGGA[C/T]AGGTTCCTGGGACAG | 23062 |
rs761488307 | snp | G/T | 1.66302e-05 | 0.00288355 | missense, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23495765 | TTCCGACATGCTTGG[G/T]TCTGTGGCTTTGTCT | 23062 |
rs761522138 | snp | C/T | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23502932 | ATGTGAGATGTCAGA[C/T]TAAGTTTTTGTGGAA | 23062 |
rs761576012 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant | GGA2 | GRCh38.p7 | 16:23488582 | AAAGGTCTGATCAGA[C/T]ACCATGTAGGTCTGT | 23062 |
rs761599174 | in-del | -/C | 0.00132048 | 0.0256612 | intron-variant | GGA2 | GRCh38.p7 | 16:23470208 | TAACACCACTACAAA[-/C]CCCCCCGGACAGCCA | 23062 |
rs761657734 | snp | A/C | 1.74506e-05 | 0.00295381 | intron-variant | GGA2 | GRCh38.p7 | 16:23483031 | GAGCTTGGTTCATGA[A/C]ACACGCCCAGGCACC | 23062 |
rs761675014 | in-del | -/TT | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511320 | ACCACACCCAGCTAT[-/TT]TTTTTTTTTTTGTAT | 23062 |
rs761697193 | snp | A/C | 1.6543e-05 | 0.00287597 | missense | GGA2 | GRCh38.p7 | 16:23482967 | CTCGCCAACCGGAAC[A/C]GCGTGGGCCGCAGCT | 23062 |
rs761712549 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23509665 | TACAGGAGACATGCA[C/G]AAGAATTCTGGCCAA | 23062 |
rs761797819 | snp | G/T | 1.64874e-05 | 0.00287113 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23493363 | CCAGGTACTCACCTT[G/T]GGGGACAACACTTTG | 23062 |
rs761825023 | snp | A/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501223 | TCCATGTGCAATCGT[A/G]GCTTTGGTGTACATC | 23062 |
rs761930898 | in-del | -/ACT | | | intron-variant | GGA2 | GRCh38.p7 | 16:23508414 | CCATTGCCTCCTAAA[-/ACT]ACTACCTTCTGTCTC | 23062 |
rs761943784 | snp | C/T | 1.71758e-05 | 0.00293046 | intron-variant | GGA2 | GRCh38.p7 | 16:23478938 | GAGTAGAGTGAGATG[C/T]CTAACAGTAACTCCA | 23062 |
rs761958917 | snp | A/G | 5.7581e-05 | 0.00536537 | intron-variant | GGA2 | GRCh38.p7 | 16:23475106 | AGCAAAAATTGTAGC[A/G]ATTTCCTGGAATCTG | 23062 |
rs761962712 | in-del | -/TC | 0.000164792 | 0.00907573 | intron-variant | GGA2 | GRCh38.p7 | 16:23494275 | CAAGGACAGGAAAGG[-/TC]TTAGGCTACAAGGCA | 23062 |
rs761971638 | in-del | -/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23468482 | ACCTGGCCGACTTTA[-/T]TTTTTTTTTGAGATG | 23062 |
rs761975985 | snp | C/T | 3.29571e-05 | 0.00405924 | missense | GGA2 | GRCh38.p7 | 16:23486055 | GCCTGCCCTGGCCTG[C/T]GGTACATGCTCAGCA | 23062 |
rs761976044 | snp | A/G | 1.648e-05 | 0.0028705 | intron-variant | GGA2 | GRCh38.p7 | 16:23494278 | AGGACAGGAAAGGTT[A/G]GGCTACAAGGCAAGC | 23062 |
rs761989040 | in-del | -/TTT | 0.00011796 | 0.00767895 | intron-variant | GGA2 | GRCh38.p7 | 16:23480608 | ATTACAGGCTGCCCC[-/TTT]AAGGCAGAGAAGGCA | 23062 |
rs762030889 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23468263 | GCTCACTGCAACCTC[C/T]GCCTCTTGGGTTCAA | 23062 |
rs762062164 | snp | C/T | 1.64841e-05 | 0.00287085 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23486138 | CTTGGACACCTTCTC[C/T]GATTTTTCTTGTTCC | 23062 |
rs762092316 | in-del | -/TTT | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511319 | CACCACACCCAGCTA[-/TTT]TTTTTTTTTTTGTAT | 23062 |
rs762172741 | snp | A/G | 4.8055e-05 | 0.00490155 | intron-variant | GGA2 | GRCh38.p7 | 16:23493551 | CTGGAGACTGCGCTG[A/G]AACCAAGGCTAACCC | 23062 |
rs762174647 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23494116 | CCCTGAAGAAACAGA[C/T]GAGAAACAGGAGGAA | 23062 |
rs762228623 | snp | A/C | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464555 | CAGAGGCATTGTCCC[A/C]AAAAAAAAAAAGCCC | 23062 |
rs762333524 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23506642 | CAACACAGAATTATC[A/G]GGCCCAAGATGTCAC | 23062 |
rs762353738 | snp | C/G | 1.69401e-05 | 0.00291029 | intron-variant | GGA2 | GRCh38.p7 | 16:23479900 | AGACTAGAAAGCCCA[C/G]GGTTAGGAAGAGAAG | 23062 |
rs762363621 | snp | A/G | 1.64838e-05 | 0.00287083 | missense | GGA2 | GRCh38.p7 | 16:23480692 | GTCACTCTGTTTCCA[A/G]AGGTGACCCGGCCCT | 23062 |
rs762383269 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23481842 | GAGAGACAGAAGAAA[C/T]ATAAACCAATTATAT | 23062 |
rs762400916 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23495360 | TGCCAGTTGCAAGTG[A/G]GCTATCCTGTGTTTT | 23062 |
rs762600055 | snp | A/G | | | synonymous-codon | GGA2 | GRCh38.p7 | 16:23488686 | TTTTATCCACTGGTA[A/G]TTTAGGGTCTTGTTT | 23062 |
rs762601848 | snp | A/G | 1.65649e-05 | 0.00287788 | missense | GGA2 | GRCh38.p7 | 16:23468933 | ATATCACAGCTGGAG[A/G]CATCAAAGGACTGAA | 23062 |
rs762620151 | snp | A/G | 3.31978e-05 | 0.00407404 | intron-variant | GGA2 | GRCh38.p7 | 16:23488727 | AAAAATGCAATTTAC[A/G]AAGTTAAGACACCGA | 23062 |
rs762699555 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23469154 | GGGAGCCCAAGCAGA[C/G]AGACTCCCACTAATT | 23062 |
rs762706616 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23470250 | GATGTACATGTTATC[C/G]CCAGATGCTGTTGCT | 23062 |
rs762708089 | snp | C/T | 8.57376e-05 | 0.00654686 | intron-variant | GGA2 | GRCh38.p7 | 16:23479920 | AGGAAGAGAAGTCAG[C/T]TGGACATGAGAGCAA | 23062 |
rs762746067 | snp | A/G | 0.00013183 | 0.00811775 | missense, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23510357 | CTGCCGGGCCCGGGG[A/G]ACCCTGGGCCGACTC | 23062 |
rs762776297 | snp | A/C | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23502801 | CCTTCTCAGTCAAAA[A/C]GGAATTTTCTGGCTT | 23062 |
rs762904170 | in-del | -/AGA | 1.70365e-05 | 0.00291855 | intron-variant | GGA2 | GRCh38.p7 | 16:23479911 | CCCAGGGTTAGGAAG[-/AGA]AGTCAGTTGGACATG | 23062 |
rs762911700 | snp | C/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501557 | AAAGCACAGAAACTG[C/G]AGGCTGTGTCATGGC | 23062 |
rs762955533 | in-del | -/AC | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467391 | CCTCTCCCCGAACAC[-/AC]ACACACACACACACA | 23062 |
rs762978005 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23490070 | CCCTCTGACAAGGGA[C/T]GGCTGTCTACTGCTA | 23062 |
rs762980783 | in-del | -/CT | | | intron-variant | GGA2 | GRCh38.p7 | 16:23482830 | GGAACCGAAAGTCCA[-/CT]CTGTCTTGTTCCTGG | 23062 |
rs762995219 | snp | A/G | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511735 | AAAAAGTATGTCATG[A/G]TTATCATAATTATGA | 23062 |
rs763021901 | snp | C/T | 0.000100125 | 0.00707478 | intron-variant | GGA2 | GRCh38.p7 | 16:23478709 | TGGTGCAACCTGTCT[C/T]CCCCAGGTATCAGCC | 23062 |
rs763133935 | snp | A/G | 1.68309e-05 | 0.00290089 | intron-variant | GGA2 | GRCh38.p7 | 16:23491839 | TTCTAGAGCTGGAAG[A/G]GACTTGGGAGACCGA | 23062 |
rs763160780 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23480232 | TTGAAAGACGCACAC[C/G]TCCAGGCCCAGCTCC | 23062 |
rs763200999 | snp | C/T | 0.00012818 | 0.00800461 | intron-variant | GGA2 | GRCh38.p7 | 16:23479048 | GAAGGTCATGTGACT[C/T]GTCCATGGCCAATCT | 23062 |
rs763264148 | snp | A/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500254 | TTGCTGGGAAGAGGT[A/T]TAAGTGCTGAGCTCT | 23062 |
rs763305922 | snp | C/G | 1.65644e-05 | 0.00287783 | intron-variant | GGA2 | GRCh38.p7 | 16:23486177 | AAAAGAGGAGGATGG[C/G]AGTGAGGGAGCAGAA | 23062 |
rs763330969 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23505234 | GGGAGTAGGACCAAG[C/T]GGAAGGAAGAAACAG | 23062 |
rs763331411 | snp | C/G/T | 7.89858e-05 | 0.00628384 | intron-variant | GGA2 | GRCh38.p7 | 16:23493566 | GAACCAAGGCTAACC[C/G/T]TGCCTCAAGCCTATG | 23062 |
rs763403713 | snp | A/G | | | synonymous-codon | GGA2 | GRCh38.p7 | 16:23474983 | AGGAGCCAACGGGCC[A/G]GCCTCCCAGGACCAA | 23062 |
rs763420724 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23487110 | CCCCAGCCTCCCAAG[G/T]AGCTGGGACTATAGG | 23062 |
rs763458932 | snp | A/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23473799 | GTTAACATCGTAACT[A/T]CAATACAGTTATTGA | 23062 |
rs763495725 | in-del | -/GAA | 1.9154e-05 | 0.00309461 | intron-variant | GGA2 | GRCh38.p7 | 16:23495817 | GAGAGTACATAATAG[-/GAA]GAAATTTACACCCCT | 23062 |
rs763495887 | snp | A/C | 3.60471e-05 | 0.00424526 | intron-variant | GGA2 | GRCh38.p7 | 16:23478319 | TCCCATGAGAAGGAA[A/C]CGCACTCAGGAGCCA | 23062 |
rs763602720 | snp | A/T | 8.28699e-05 | 0.00643647 | missense, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23495757 | CAATCCTGTTCCGAC[A/T]TGCTTGGGTCTGTGG | 23062 |
rs763605419 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23481989 | AAATGTCCAGAGGCC[A/G]GGGATCGTGGCTCAC | 23062 |
rs763627597 | snp | A/C | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23502841 | AAAGTGCTGAGGATC[A/C]ACTGCCCCAGAGTCT | 23062 |
rs763638499 | snp | C/G | 1.64735e-05 | 0.00286993 | missense | GGA2 | GRCh38.p7 | 16:23486759 | GCCTGAAGGTCCTCG[C/G]GGTGGTTGCTCTTTA | 23062 |
rs763648966 | snp | A/G | 1.65512e-05 | 0.00287669 | intron-variant | GGA2 | GRCh38.p7 | 16:23494393 | GCTACAGGGAAACAA[A/G]AAGACCTAGACTCTG | 23062 |
rs763704466 | snp | A/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499974 | CAGATTGGTTCCTGG[A/G]AACCAGGAGAGAGCT | 23062 |
rs763707671 | snp | A/G | 0.000213911 | 0.0103397 | intron-variant | GGA2 | GRCh38.p7 | 16:23478558 | TGACCATCAGCCACA[A/G]TAAAACCAAGGCACA | 23062 |
rs763726112 | snp | C/G | 2.14687e-05 | 0.00327626 | intron-variant | GGA2 | GRCh38.p7 | 16:23479083 | CTAATATGCAAGGGG[C/G]ACCCTCTGAACTGCC | 23062 |
rs763730219 | snp | A/G | 1.6473e-05 | 0.00286988 | intron-variant | GGA2 | GRCh38.p7 | 16:23488575 | TAAGAGAAAAGGTCT[A/G]ATCAGACACCATGTA | 23062 |
rs763775414 | snp | A/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501574 | GGCTGTGTCATGGCC[A/G]TGTGAATACAAAGAC | 23062 |
rs763793027 | snp | C/T | 3.71996e-05 | 0.00431259 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23467611 | TGCGCCCAAGACAGC[C/T]AGGTCTGGGAAGTCT | 23062 |
rs763821574 | snp | A/G/T | 9.92087e-05 | 0.00704241 | missense, synonymous-codon | GGA2 | GRCh38.p7 | 16:23482963 | GTCACTCGCCAACCG[A/G/T]AACAGCGTGGGCCGC | 23062 |
rs763882778 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23508173 | AAGGGTTCAAGTGAT[A/C]CTCCCACCTCGGCCT | 23062 |
rs763901655 | snp | A/G | 1.66624e-05 | 0.00288633 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23478442 | GTTCTGAACACCACC[A/G]CCTGGCAGCGTGCTG | 23062 |
rs763923745 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23478136 | CTCAGGAGGTAAAGG[C/T]TGTAGTGAGCCGAGA | 23062 |
rs763927624 | snp | A/G | 1.64871e-05 | 0.00287111 | missense | GGA2 | GRCh38.p7 | 16:23480755 | GTGAGGAGGTCATTT[A/G]CCTGGAGAATTTCCG | 23062 |
rs763976857 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23490087 | GCTGTCTACTGCTAC[A/G]AGTGGCAAGAACAAG | 23062 |
rs764079876 | snp | A/G | 1.66192e-05 | 0.00288259 | intron-variant | GGA2 | GRCh38.p7 | 16:23491813 | GTACTGAAAGTAAAA[A/G]GGAAAGAGAATTCTA | 23062 |
rs764107325 | snp | C/G | 3.71099e-05 | 0.00430738 | intron-variant | GGA2 | GRCh38.p7 | 16:23478818 | TCGCCAGGCAGTGCT[C/G]CCTCACAAGGGCAGG | 23062 |
rs764119943 | in-del | -/GTGTGTGTGTGTGTGTGTGT | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510909 | ACTGGGTTTCACCGT[-/GTGTGTGTGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 23062 |
rs764126453 | snp | C/G | 0.000390168 | 0.0139618 | utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23510420 | CCGCCATCGCTCCAG[C/G]CCCGACGCTGCGGCC | 23062 |
rs764131994 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23477364 | CCATACTGTTCTCAC[A/G]GTAGTAAGTCTCATG | 23062 |
rs764177867 | snp | C/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499411 | AGCCTCCCAAAGTAG[C/T]GGGATTACAGGTGTG | 23062 |
rs764295239 | snp | C/T | 1.94362e-05 | 0.00311732 | intron-variant | GGA2 | GRCh38.p7 | 16:23467744 | ATCAGTGGAGAGCAA[C/T]CCAGGAACAGGGGTC | 23062 |
rs764348302 | in-del | -/AAC | | | intron-variant | GGA2 | GRCh38.p7 | 16:23506372 | CTACTCCCAGAAGAA[-/AAC]AACAACAAATACAGC | 23062 |
rs764355763 | in-del | -/GCCCC | 0.000118238 | 0.00768799 | intron-variant | GGA2 | GRCh38.p7 | 16:23480604 | TGGGAATTACAGGCT[-/GCCCC]AAGGCAGAGAAGGCA | 23062 |
rs764361004 | snp | C/G | 1.89943e-05 | 0.00308168 | intron-variant | GGA2 | GRCh38.p7 | 16:23483055 | AGGCACCCCATAACG[C/G]CCCCCTCCAGGGCCC | 23062 |
rs764361240 | snp | A/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23473860 | TTTCTTAAATCAAAA[A/T]TCAATAAAGAAATGT | 23062 |
rs764416125 | snp | A/G | 1.64779e-05 | 0.00287031 | missense | GGA2 | GRCh38.p7 | 16:23486056 | CCTGCCCTGGCCTGC[A/G]GTACATGCTCAGCAT | 23062 |
rs764480613 | snp | A/G | 1.75305e-05 | 0.00296056 | intron-variant | GGA2 | GRCh38.p7 | 16:23493488 | GACCCCCAGGAGAAG[A/G]TGGAAAGCCAGTGGT | 23062 |
rs764534799 | snp | A/G | 4.94409e-05 | 0.00497172 | missense | GGA2 | GRCh38.p7 | 16:23474970 | GTGAAGATGGGGAAG[A/G]AGCCAACGGGCCAGC | 23062 |
rs764580016 | snp | A/G | 3.30028e-05 | 0.00406205 | intron-variant | GGA2 | GRCh38.p7 | 16:23474892 | AAAGGTGGGGAGTGA[A/G]ATTGTACTTACTGGG | 23062 |
rs764580614 | snp | A/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23481172 | TCACCTGAGGTCAGG[A/T]GTTCGAGACTATCCT | 23062 |
rs764632043 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23493040 | GGCAGGAGGTGATAG[A/G]AAACTTTCACGCCAC | 23062 |
rs764657286 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23493926 | TAAACACTCAAACAT[A/C]TACAAAGACCTAAAC | 23062 |
rs764749926 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23492934 | CCAGCATCGGCACTG[C/T]TGTGGGAACACAACA | 23062 |
rs764765850 | snp | C/G | 1.7801e-05 | 0.00298332 | intron-variant | GGA2 | GRCh38.p7 | 16:23467704 | GCGGATAGGTTCCTG[C/G]GACAGAAGAGACAGA | 23062 |
rs764773602 | snp | C/G | 1.65048e-05 | 0.00287265 | missense | GGA2 | GRCh38.p7 | 16:23479804 | GCAAAGATGGCACCA[C/G]AGTCCCCATCTGCGC | 23062 |
rs764787061 | in-del | -/AC | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467390 | ACCCTCTCCCCGAAC[-/AC]ACACACACACACACA | 23062 |
rs764788101 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant | GGA2 | GRCh38.p7 | 16:23488584 | AGGTCTGATCAGACA[C/T]CATGTAGGTCTGTTT | 23062 |
rs764839398 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23480996 | CAAATCTGTTCACCT[C/T]CTACACCTGTACTGT | 23062 |
rs764863145 | snp | A/G | 1.69596e-05 | 0.00291196 | intron-variant | GGA2 | GRCh38.p7 | 16:23479902 | ACTAGAAAGCCCAGG[A/G]TTAGGAAGAGAAGTC | 23062 |
rs764863546 | snp | A/G | 1.64827e-05 | 0.00287073 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23474911 | GTACTTACTGGGCTT[A/G]ACAGACTCCAAAGGG | 23062 |
rs764888001 | in-del | -/TTTT | | | intron-variant | GGA2 | GRCh38.p7 | 16:23472185 | TCTTTGTAGCCCTGG[-/TTTT]TTTTTTTTTTTTTTT | 23062 |
rs764929911 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23481813 | GCAGAGGGCATGCAC[A/G]TGCTATCCACTAAGA | 23062 |
rs764963828 | snp | A/G | 1.73601e-05 | 0.00294614 | intron-variant | GGA2 | GRCh38.p7 | 16:23478705 | AGCCTGGTGCAACCT[A/G]TCTCCCCCAGGTATC | 23062 |
rs764984753 | snp | C/T | 3.33161e-05 | 0.00408129 | missense, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23495767 | CCGACATGCTTGGGT[C/T]TGTGGCTTTGTCTGT | 23062 |
rs765027423 | in-del | -/G | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503850 | ATTTTGGGAGGCCAA[-/G]GTGGGCGGATCACCT | 23062 |
rs765034623 | snp | A/G | 3.32237e-05 | 0.00407563 | intron-variant | GGA2 | GRCh38.p7 | 16:23494412 | ACCTAGACTCTGGGC[A/G]GGCAAAAAGAAACTA | 23062 |
rs765093809 | snp | A/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23468642 | CCACAACCAGCTAAT[A/T]TTTGTATTTTTAGTA | 23062 |
rs765110142 | in-del | -/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23474195 | GAATTCTACCTCTTG[-/C]CAGTCATTTCAGGCC | 23062 |
rs765138282 | snp | A/C/G | 0.000810212 | 0.0201112 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23479850 | CTCCAAGTCAATCAG[A/C/G]GGGCAGGTCTTCATG | 23062 |
rs765140426 | snp | A/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501296 | AATTGGAAAAAGATT[A/G]TCCTTGGAGCCATGC | 23062 |
rs765245590 | snp | C/T | 3.3094e-05 | 0.00406766 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23482969 | CGCCAACCGGAACAG[C/T]GTGGGCCGCAGCTTT | 23062 |
rs765246769 | snp | C/T | 1.71879e-05 | 0.00293149 | missense | GGA2 | GRCh38.p7 | 16:23470019 | CAGCCACTTGAAACA[C/T]GATATCCCAGACAGG | 23062 |
rs765262528 | snp | C/T | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465855 | CTGAGGCACGAGAAT[C/T]GCTTGAACCTGGTAG | 23062 |
rs765264825 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23496031 | CTGGCTGGGCACAGT[C/G]GCTCATGCCTGTAAT | 23062 |
rs765286087 | snp | C/T | 0.000110572 | 0.00743463 | intron-variant | GGA2 | GRCh38.p7 | 16:23478589 | GCTCTCCTGAGCCCA[C/T]CCAAGCTGCTGTGGC | 23062 |
rs765318543 | in-del | -/C | 1.648e-05 | 0.0028705 | splice-donor-variant | GGA2 | GRCh38.p7 | 16:23494302 | GGCAAGCCAAACTCA[-/C]CGTTAAGGCATAAAG | 23062 |
rs765371148 | snp | C/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499030 | GGGGAGGCAGGGAGA[C/G]AACAGGAGAGGCAGA | 23062 |
rs765394137 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23509503 | CTAAAAAATGTTTTG[A/G]TGAGCAAGGACCCTG | 23062 |
rs765427842 | snp | A/G | 3.30836e-05 | 0.00406702 | intron-variant | GGA2 | GRCh38.p7 | 16:23486165 | TTCCTTTTGGGAAAA[A/G]GAGGAGGATGGGAGT | 23062 |
rs765445708 | snp | C/T | 1.72725e-05 | 0.0029387 | intron-variant | GGA2 | GRCh38.p7 | 16:23478939 | AGTAGAGTGAGATGC[C/T]TAACAGTAACTCCAC | 23062 |
rs765478283 | snp | A/G | 0.000124174 | 0.00787855 | intron-variant | GGA2 | GRCh38.p7 | 16:23478827 | AGTGCTGCCTCACAA[A/G]GGCAGGTCTGAGACC | 23062 |
rs765528889 | snp | C/T | 6.78587e-05 | 0.0058245 | intron-variant | GGA2 | GRCh38.p7 | 16:23493560 | GCGCTGGAACCAAGG[C/T]TAACCCTGCCTCAAG | 23062 |
rs765554500 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23484461 | TTCAAAAGATGCTAT[C/T]AAAATAGTGAAAAGA | 23062 |
rs765564100 | snp | C/T | 1.6617e-05 | 0.00288239 | missense | GGA2 | GRCh38.p7 | 16:23468983 | GATGCCGGCTGCAGC[C/T]TCACTCTCATTGACT | 23062 |
rs765638642 | in-del | -/G | 1.65614e-05 | 0.00287757 | intron-variant | GGA2 | GRCh38.p7 | 16:23480617 | CTGCCCCAAGGCAGA[-/G]AAGGCAAGGAGAAGC | 23062 |
rs765656127 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23473495 | GTGTACATTACCACA[C/T]CCAGCTAATTTTTAT | 23062 |
rs765665771 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23492484 | AAAACAAAACAAAAC[A/C]AAAAAACCTCAGATG | 23062 |
rs765709055 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23485842 | CAGCTGCCTGGGGAC[C/T]GGGGAGCAAGGGACA | 23062 |
rs765710993 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23472019 | TATGGGGAAAAAAAG[C/G]AACCTTTTCAGACGG | 23062 |
rs765734680 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23474888 | AAAAAAAGGTGGGGA[A/G]TGAAATTGTACTTAC | 23062 |
rs765794516 | snp | A/G | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504404 | CTCTCACAGGCTCTA[A/G]TACCTAGAAGAGTTG | 23062 |
rs765809092 | snp | A/G | 1.64817e-05 | 0.00287064 | missense | GGA2 | GRCh38.p7 | 16:23474978 | GGGGAAGGAGCCAAC[A/G]GGCCAGCCTCCCAGG | 23062 |
rs765838873 | snp | C/T | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504294 | TTGCGGTGAGGTCTT[C/T]AGTTCCTTGACAAAG | 23062 |
rs765846688 | snp | A/C | 4.94507e-05 | 0.00497221 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23480700 | GTTTCCAAAGGTGAC[A/C]CGGCCCTCCATCACC | 23062 |
rs765932309 | snp | A/G | 3.44483e-05 | 0.00415006 | intron-variant | GGA2 | GRCh38.p7 | 16:23479922 | GAAGAGAAGTCAGTT[A/G]GACATGAGAGCAAAG | 23062 |
rs765999790 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23492039 | GAGCCTGGGTCAGAG[C/T]CTGTTCTACACCACT | 23062 |
rs766028845 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23509152 | CAGATTCTCCGGCTG[A/C]AAACTCCCAAACAGC | 23062 |
rs766092416 | in-del | -/CACACACACAAAAACAG | | | intron-variant | GGA2 | GRCh38.p7 | 16:23470781 | AAAAACAAAAAGCCA[-/CACACACACAAAAACAG]GATTATCATTAAAAA | 23062 |
rs766104456 | snp | C/G | 1.65636e-05 | 0.00287776 | missense | GGA2 | GRCh38.p7 | 16:23468937 | CACAGCTGGAGGCAT[C/G]AAAGGACTGAATGCA | 23062 |
rs766109591 | snp | C/T | 0.000301523 | 0.0122748 | missense, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23510387 | CGGTTCCCGCCACAG[C/T]CGCCGCCACCGCGGT | 23062 |
rs766198248 | snp | G/T | 1.66463e-05 | 0.00288494 | intron-variant | GGA2 | GRCh38.p7 | 16:23488732 | TGCAATTTACAAAGT[G/T]AAGACACCGATATGG | 23062 |
rs766211941 | snp | A/G | | | synonymous-codon | GGA2 | GRCh38.p7 | 16:23480673 | GATGTCTCCCAATGA[A/G]CTGGTCACTCTGTTT | 23062 |
rs766278554 | snp | C/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466192 | TTGTAATTAAGAGCT[C/G]CAAACAAGTCTTGCA | 23062 |
rs766302479 | snp | A/G | 1.73327e-05 | 0.00294381 | intron-variant | GGA2 | GRCh38.p7 | 16:23495786 | GGCTTTGTCTGTCAA[A/G]TAAATAATAAAGTTA | 23062 |
rs766351449 | snp | C/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499600 | CTCAATCAAGATTTA[C/T]TGGTAATCCCAGAAC | 23062 |
rs766395381 | snp | C/T | 3.44406e-05 | 0.00414959 | intron-variant | GGA2 | GRCh38.p7 | 16:23478712 | TGCAACCTGTCTCCC[C/T]CAGGTATCAGCCAGA | 23062 |
rs766537286 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23506792 | AATACTCAGGTGGCA[A/G]TGGTGGCACTGACGA | 23062 |
rs766564208 | snp | A/G | 0.000129057 | 0.00803193 | intron-variant | GGA2 | GRCh38.p7 | 16:23479049 | AAGGTCATGTGACTC[A/G]TCCATGGCCAATCTG | 23062 |
rs766589249 | snp | A/G | 1.65655e-05 | 0.00287793 | intron-variant | GGA2 | GRCh38.p7 | 16:23486178 | AAAGAGGAGGATGGG[A/G]GTGAGGGAGCAGAAA | 23062 |
rs766600629 | snp | C/G | 1.64871e-05 | 0.00287111 | missense | GGA2 | GRCh38.p7 | 16:23493365 | AGGTACTCACCTTTG[C/G]GGACAACACTTTGAT | 23062 |
rs766654195 | snp | C/G | 1.72528e-05 | 0.00293703 | missense | GGA2 | GRCh38.p7 | 16:23470160 | CAATGAGAGGCGGCA[C/G]GCTGCCTGGTATAAA | 23062 |
rs766683987 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23507874 | GATGTGGGAAAAATG[C/T]TTGAGCCCAGGAGAG | 23062 |
rs766777220 | in-del | -/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23486494 | TTGAGCAGCATGGAT[-/G]AAAGCAGCTGAGAAG | 23062 |
rs766785841 | snp | A/G | 1.648e-05 | 0.0028705 | missense, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23494304 | CAAGCCAAACTCACC[A/G]TTAAGGCATAAAGAG | 23062 |
rs766841725 | snp | A/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23470571 | AGTTCAAGACCAGCC[A/T]GGACAACATGGCAAA | 23062 |
rs766873419 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23497625 | TCTCTCCCATGTTCC[A/G]TATCTTAAAATCCTA | 23062 |
rs766875480 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23483102 | GGCAGACGGCAGAGT[A/C]TGGGGCTTCAGAAGG | 23062 |
rs766898824 | snp | A/G | 1.64754e-05 | 0.00287009 | missense | GGA2 | GRCh38.p7 | 16:23486070 | CGGTACATGCTCAGC[A/G]TCTCCTGCAGCACCT | 23062 |
rs766977534 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23471773 | TTGCTGGGTGTGGTG[A/G]TGCATGCCTGTCATT | 23062 |
rs767061407 | in-del | -/ACTG | 0.000232369 | 0.0107764 | splice-donor-variant | GGA2 | GRCh38.p7 | 16:23510319 | CCTGCCAGGCTACTC[-/ACTG]AGCCACAGCTCCAGC | 23062 |
rs767084209 | snp | A/G | 1.64817e-05 | 0.00287064 | missense, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23494314 | TCACCGTTAAGGCAT[A/G]AAGAGCTTCCTTCTC | 23062 |
rs767090845 | snp | C/T | 1.66333e-05 | 0.00288381 | intron-variant | GGA2 | GRCh38.p7 | 16:23486197 | AGGGAGCAGAAACCC[C/T]GGCTGAAGCCTGAAC | 23062 |
rs767132563 | snp | C/T | 1.67708e-05 | 0.00289571 | intron-variant | GGA2 | GRCh38.p7 | 16:23482876 | AGGAGGGACCGAGTC[C/T]GTCTTGCACCTGGGC | 23062 |
rs767138967 | in-del | -/T/TT | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511502 | GTTTTCCTGGAACAC[-/T/TT]TTTTTTTTTTTTTCA | 23062 |
rs767218487 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23471887 | GCACTCCTGCCTAGG[C/T]GATGGAGCGAGGCCC | 23062 |
rs767242790 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | GGA2 | GRCh38.p7 | 16:23491712 | TAAGCGTCTCGAATC[C/T]TGATGTCTTCCGGAA | 23062 |
rs767270155 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23490231 | AGAGGAATCTGAAGT[C/G]TGATATAGTAACTAC | 23062 |
rs767297240 | snp | C/T | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465187 | GACACGGTCTCACTA[C/T]GTAGCCCAGGCTGGA | 23062 |
rs767328634 | snp | A/T | 1.64811e-05 | 0.00287059 | missense | GGA2 | GRCh38.p7 | 16:23480741 | GCAGAACTCCTTGGG[A/T]GAGGAGGTCATTTGC | 23062 |
rs767372033 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23497970 | GAGACCCAATCTCCA[C/T]AGAAATTTTTAAAAA | 23062 |
rs767373640 | snp | A/G | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23512123 | CACCATGTTTGAAAG[A/G]CGGAAGAAGAGACCC | 23062 |
rs767431381 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23491966 | CCCAGCCCCGGAGCC[C/T]TTCCTGGGATTCAAG | 23062 |
rs767434964 | snp | C/T | 1.67237e-05 | 0.00289164 | intron-variant | GGA2 | GRCh38.p7 | 16:23488740 | ACAAAGTTAAGACAC[C/T]GATATGGTACCCAGA | 23062 |
rs767609045 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23487397 | TGCTACTGGCAGCTC[A/G]TGGGTAGAGTGAGGA | 23062 |
rs767623820 | snp | C/T | 3.53544e-05 | 0.00420428 | intron-variant | GGA2 | GRCh38.p7 | 16:23469993 | CCCCAACAGATGACT[C/T]ACCTTTGGCACAGCC | 23062 |
rs767624648 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23476762 | TTGCACTTTGTTGTA[C/T]GTTTCTCCATGGATC | 23062 |
rs767681621 | in-del | -/TTG | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511331 | CTATTTTTTTTTTTT[-/TTG]TATTTTTAGTAGAAA | 23062 |
rs767734318 | snp | G/T | 0.000386304 | 0.0138925 | intron-variant | GGA2 | GRCh38.p7 | 16:23478602 | CACCCAAGCTGCTGT[G/T]GCCCAGACTGGTGAC | 23062 |
rs767773367 | snp | C/T | 1.64822e-05 | 0.00287068 | missense | GGA2 | GRCh38.p7 | 16:23493377 | TTGGGGACAACACTT[C/T]GATCAGTTCGTTCAG | 23062 |
rs767876676 | snp | C/T | | | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463379 | AGCTATCTATGGTGT[C/T]ACATGAAAAGAACAA | 23062 |
rs767889220 | snp | A/G | 1.74876e-05 | 0.00295694 | intron-variant | GGA2 | GRCh38.p7 | 16:23470173 | CAGGCTGCCTGGTAT[A/G]AAGGGCACAAGCAGA | 23062 |
rs767897040 | snp | A/G | 1.64732e-05 | 0.0028699 | missense | GGA2 | GRCh38.p7 | 16:23486751 | GGTTTGCAGCCTGAA[A/G]GTCCTCGGGGTGGTT | 23062 |
rs767943294 | snp | C/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466232 | GTAGAAACCCACCCA[C/G]CCAGTTCAGCTGCTT | 23062 |
rs767948026 | snp | A/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23482166 | CTACTTGGGAGGCTG[A/T]GGAAGGAGAATGGCT | 23062 |
rs767952498 | in-del | -/AAAAAAAAAAAAAAGAAAAAAAGAC | | | intron-variant | GGA2 | GRCh38.p7 | 16:23478201 | GAGACCCCGTCTCAA[-/AAAAAAAAAAAAAAGAAAAAAAGAC]AAAAAAAAAAAAAAG | 23062 |
rs768064748 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23495274 | ATTAGGTAACGTGTC[C/T]ATAGTCTATCAGTAA | 23062 |
rs768112093 | snp | C/T | 3.31609e-05 | 0.00407177 | missense | GGA2 | GRCh38.p7 | 16:23482923 | GGAAAGAAAACTTAC[C/T]GAGTGCATCATCGTC | 23062 |
rs768157448 | snp | A/G | 1.73096e-05 | 0.00294185 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23467688 | TCAGCTTGTACCGTA[A/G]GCGGATAGGTTCCTG | 23062 |
rs768203505 | in-del | -/GTAA | | | intron-variant | GGA2 | GRCh38.p7 | 16:23491051 | ATACAAATATTTGGT[-/GTAA]GTGAGACAGCAAGTG | 23062 |
rs768223728 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23508803 | TCTCTTTTTTGACTA[C/T]GCCACAAGCACCTCA | 23062 |
rs768229517 | in-del | -/TTTGTA | 3.56157e-05 | 0.00421978 | intron-variant | GGA2 | GRCh38.p7 | 16:23470190 | GGGCACAAGCAGAAG[-/TTTGTA]GTTTAACACCACTAC | 23062 |
rs768271562 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23483796 | GGGATTACAGGCATG[C/T]GCCACCACGCCCGGC | 23062 |
rs768323973 | snp | A/G | 3.40194e-05 | 0.00412414 | intron-variant | GGA2 | GRCh38.p7 | 16:23483013 | ACACGACCTGAAAGA[A/G]CAGAGCTTGGTTCAT | 23062 |
rs768335681 | snp | A/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464336 | ATCAGGGCTTGAAAG[A/G]ACTTTATTGTGGCTG | 23062 |
rs768354615 | in-del | -/AAAT | | | intron-variant | GGA2 | GRCh38.p7 | 16:23484630 | GCCAATGAGCATAGG[-/AAAT]AAATAAGCCATCAAG | 23062 |
rs768357510 | snp | C/G | 0.00087587 | 0.0209086 | intron-variant | GGA2 | GRCh38.p7 | 16:23478681 | CTGGGCAGACCTCCA[C/G]GAAGCAGGAGCCTGG | 23062 |
rs768423459 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23490950 | GGGCATGGTGGCTCA[C/T]GCCTGGGAGGCTGTG | 23062 |
rs768502846 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23471689 | AAAACTGCTTGAGGT[A/C]AGGAGTTCAAAACCA | 23062 |
rs768532970 | snp | A/T | 1.66613e-05 | 0.00288623 | intron-variant | GGA2 | GRCh38.p7 | 16:23474859 | GGGAGTCTAATAGAT[A/T]CCCAGGGAAAAAAAA | 23062 |
rs768575514 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23467867 | ATCCTGGGAACCCTT[C/T]GATAATTCTGCAGTC | 23062 |
rs768656493 | snp | A/G | 1.64819e-05 | 0.00287066 | intron-variant | GGA2 | GRCh38.p7 | 16:23494269 | TATAGCACAAGGACA[A/G]GAAAGGTTAGGCTAC | 23062 |
rs768700830 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23491696 | TTTCTTCAGCATCTG[A/G]TAAGCGTCTCGAATC | 23062 |
rs768700924 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23504703 | GGGCCAGACAGGGCA[C/T]GGCCAGGGAGAAATT | 23062 |
rs768722647 | snp | A/G | 1.81013e-05 | 0.00300838 | intron-variant | GGA2 | GRCh38.p7 | 16:23475085 | AAATAAAAAATATCA[A/G]AGACTAGCAAAAATT | 23062 |
rs768726964 | in-del | -/AC | 1.65392e-05 | 0.00287564 | intron-variant | GGA2 | GRCh38.p7 | 16:23493327 | GTGGGCGTAGGTGCG[-/AC]ACAGTCAGCAGAGCC | 23062 |
rs768760041 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23485949 | CTTCATGGGTGCAAA[C/T]AGGTGAAAGCATTTC | 23062 |
rs768823095 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23497591 | GATTCCTATATTCTC[C/T]TCCCCACCCCCGCAA | 23062 |
rs768842911 | snp | A/C | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467044 | CAGAACACACACAAG[A/C]AGCATTGTCTAATGA | 23062 |
rs768850795 | snp | A/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501119 | ACTTTCACAAGAGAA[A/G]GTTCCAGGGAAATCC | 23062 |
rs768866242 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23481547 | GGAAGCCAAGGCGGG[A/C]AAATCACTTGAGCCC | 23062 |
rs768898153 | snp | C/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500742 | GGCAGTAGCGCCACA[C/T]CCCACTGCTGTGGAG | 23062 |
rs768898213 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23469702 | CCATGCAACCCTGGA[A/G]CTGTGGGTAGCCACT | 23062 |
rs769012571 | snp | A/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23476611 | TGCATCACAGATATA[A/T]TATGAAAAGGTCATG | 23062 |
rs769017795 | in-del | -/TTT | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511164 | ATTTTTCTTTTTTTC[-/TTT]TTTTGAGACGGAGTC | 23062 |
rs769058627 | in-del | -/A | | | intron-variant | GGA2 | GRCh38.p7 | 16:23483994 | CACCAGGAAGACATT[-/A]AAAAAAAAAAAAGGC | 23062 |
rs769213336 | snp | A/G | 3.29457e-05 | 0.00405854 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23491702 | CAGCATCTGATAAGC[A/G]TCTCGAATCTTGATG | 23062 |
rs769265027 | snp | C/T | 3.29473e-05 | 0.00405864 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23488684 | GATTTTATCCACTGG[C/T]AGTTTAGGGTCTTGT | 23062 |
rs769301088 | in-del | -/C | 1.6483e-05 | 0.00287076 | frameshift-variant | GGA2 | GRCh38.p7 | 16:23486135 | CCTCTTGGACACCTT[-/C]TCCGATTTTTCTTGT | 23062 |
rs769357196 | snp | G/T | 1.64732e-05 | 0.0028699 | missense | GGA2 | GRCh38.p7 | 16:23491689 | GACCTTGTTTCTTCA[G/T]CATCTGATAAGCGTC | 23062 |
rs769358855 | snp | A/G | 3.37268e-05 | 0.00410637 | intron-variant | GGA2 | GRCh38.p7 | 16:23479895 | CTGAAAGACTAGAAA[A/G]CCCAGGGTTAGGAAG | 23062 |
rs769436325 | snp | C/G/T | 1.70067e-05 | 0.002916 | missense | GGA2 | GRCh38.p7 | 16:23470145 | CATTCCGGTCATACA[C/G/T]AATGAGAGGCGGCAG | 23062 |
rs769454300 | snp | C/T | 1.64751e-05 | 0.00287007 | intron-variant | GGA2 | GRCh38.p7 | 16:23478796 | CAGTGCAGGAGCACC[C/T]CTCTGCTCGCCAGGC | 23062 |
rs769473951 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23507232 | TTTCACTTAAGAATA[C/T]AGGTTCTAGCCGTTC | 23062 |
rs769476854 | snp | A/G | 0.00243249 | 0.0347898 | missense, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23510347 | TCCAGCGACGCTGCC[A/G]GGCCCGGGGGACCCT | 23062 |
rs769478175 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23493843 | CACTCAAGAGGCAAG[A/C]TGAGCCTGCAGACCC | 23062 |
rs769481008 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23482713 | ATTTCCACTTCTTTT[C/T]AGGCTTTAGACCTGC | 23062 |
rs769493928 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23476458 | TTCAGGGATCTATAC[C/T]ATAAGGCACTCCCCC | 23062 |
rs769550020 | snp | A/T | 3.31241e-05 | 0.00406952 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23468919 | CAGCAGCATCTGAGA[A/T]ATCACAGCTGGAGGC | 23062 |
rs769558301 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23485363 | CTCATAAAGATGCTA[C/T]ATAAAAACCAAGATC | 23062 |
rs769582824 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23483584 | AGAGTTCCAAGGGAG[A/G]CCAACAGCATGGCTG | 23062 |
rs769588065 | in-del | -/A | 1.6537e-05 | 0.00287545 | frameshift-variant | GGA2 | GRCh38.p7 | 16:23479848 | ACCTCCAAGTCAATC[-/A]GGGGGCAGGTCTTCA | 23062 |
rs769710624 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23480102 | CTTCCTACCCCAGGG[A/C]TCATAGGCCCTCCTG | 23062 |
rs769749726 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23471383 | GAGGGGGGAAAACTA[C/T]GTAAGACTGACCAAT | 23062 |
rs769753123 | in-del | -/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23483229 | TAAAATAATCTGACC[-/G]GGCAGGGTGGCTCAC | 23062 |
rs769769715 | snp | C/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23502584 | GCAACTCACATTTTC[C/T]AGTGCACCTCAGTGG | 23062 |
rs769872141 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23497220 | GAGCAGCTCTTTTAG[A/G]CTCTGGAAATGAGGC | 23062 |
rs769879117 | snp | C/T | 1.64743e-05 | 0.00287 | intron-variant | GGA2 | GRCh38.p7 | 16:23486805 | GCTGCAGAGAGTGAA[C/T]AGGAAGAGTAGGTGA | 23062 |
rs769887189 | snp | C/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466763 | ATGGTGTGTCACAAA[C/G]AGCTCCAAGTAAATG | 23062 |
rs769921098 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23479463 | CCTCAGCAGCAGGTA[C/T]GTGCTCCCTCAGCAG | 23062 |
rs769933334 | snp | A/T | 7.3252e-05 | 0.0060515 | intron-variant | GGA2 | GRCh38.p7 | 16:23479034 | ATAAGCAACTTACTG[A/T]AGGTCATGTGACTCG | 23062 |
rs769985232 | snp | C/T | 1.65031e-05 | 0.00287251 | synonymous-codon, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23494354 | CTGGATCTTGTGGGC[C/T]AGTAGCCAGGGCGCA | 23062 |
rs769993478 | in-del | -/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23476222 | AAATAACCCACCCTG[-/C]CCCGAGTGGCTGAAA | 23062 |
rs769994440 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23492727 | TATGGAATATGGGGC[A/G]GTGGGGGTCATAGGA | 23062 |
rs770009985 | snp | C/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501039 | GTGACTTGGGCAATA[C/T]ATTACAACATAAAGC | 23062 |
rs770071501 | snp | A/T | 1.6473e-05 | 0.00286988 | missense | GGA2 | GRCh38.p7 | 16:23486731 | GACCAAATTCTTGAT[A/T]AACCGGTTTGCAGCC | 23062 |
rs770099397 | snp | A/G | 1.69163e-05 | 0.00290824 | intron-variant | GGA2 | GRCh38.p7 | 16:23478518 | TGTCAAATCAGGAAT[A/G]GCTAAAATAAGACCA | 23062 |
rs770177885 | snp | C/G | 1.64803e-05 | 0.00287052 | intron-variant | GGA2 | GRCh38.p7 | 16:23494279 | GGACAGGAAAGGTTA[C/G]GCTACAAGGCAAGCC | 23062 |
rs770178242 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23488218 | CACCCACACTCCCCA[C/T]GGGCTATCCTTCTGC | 23062 |
rs770200592 | in-del | -/TTTA | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511146 | TGCTTGCATTTATTT[-/TTTA]TTTTTCTTTTTTTCT | 23062 |
rs770244311 | in-del | -/TGT | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503656 | CACAAGAACTTAAAA[-/TGT]TGTGTAAAATACTTC | 23062 |
rs770264422 | snp | A/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467541 | CCTGACTAGACAGCA[A/G]AAGTAACGCCAGCCT | 23062 |
rs770295812 | snp | A/C/G | 0.000116842 | 0.00764255 | missense | GGA2 | GRCh38.p7 | 16:23478396 | CTGGCTGTGCTGAGA[A/C/G]GAGGTCCAGCAAATT | 23062 |
rs770309577 | snp | A/G | 3.29457e-05 | 0.00405854 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23491756 | ACTGAAGAGTATTTC[A/G]ATGACTCTTCCTTTA | 23062 |
rs770357353 | snp | A/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23508298 | CTTAAACTCCTGGCC[A/T]CAAAGGATTGGCCCA | 23062 |
rs770357700 | snp | C/T | 3.29582e-05 | 0.00405931 | missense | GGA2 | GRCh38.p7 | 16:23491775 | ACTCTTCCTTTAACT[C/T]TTCCTGTGGCCCAGG | 23062 |
rs770426205 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23474748 | TGAGTCACCATACCT[A/G]GCCACAACCTCTTAC | 23062 |
rs770570050 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23505645 | AGGTCCCCCATTCAC[C/T]CTCCCCACCTTTGGC | 23062 |
rs770571675 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23486481 | TCTAGGAAATGCTTT[C/G]AGCAGCATGGATGAA | 23062 |
rs770573317 | snp | A/G | 1.79181e-05 | 0.00299311 | intron-variant | GGA2 | GRCh38.p7 | 16:23469965 | TCAAAAACGACAGCC[A/G]TTACTGAGAAATCCC | 23062 |
rs770593101 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23481687 | CTGAGGCATGAGAAT[C/T]GCTTGAACACAGGAT | 23062 |
rs770593650 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23482243 | CACTCTAACCTGGAC[A/G]ACAGAGCGAGACTCC | 23062 |
rs770619338 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23505132 | TCCCTGGGAGGGACA[C/T]GTGGACCCCAAGAGT | 23062 |
rs770621019 | snp | C/T | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465223 | AATCCTGGGCTCAAG[C/T]GGTCATCCCACTCAG | 23062 |
rs770646078 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23493636 | AAGAAAAAAATGTCC[C/G]CTGTTCAATCTTGCT | 23062 |
rs770670634 | in-del | -/A | | | intron-variant | GGA2 | GRCh38.p7 | 16:23482571 | GGCCCCTGAAGGTAC[-/A]AAAAGCCCGTGATCC | 23062 |
rs770674584 | in-del | -/A | 1.67452e-05 | 0.0028935 | intron-variant | GGA2 | GRCh38.p7 | 16:23480601 | TCTGGGAATTACAGG[-/A]CTGCCCCAAGGCAGA | 23062 |
rs770720244 | snp | A/C | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464742 | GAAAGGGGCAGGACT[A/C]TGGGTTCCATTCTAA | 23062 |
rs770720448 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23494742 | GCAGAAAGTGCGATC[A/C]AACTCTGGGTTCAAA | 23062 |
rs770752427 | snp | C/G/T | 0.000922668 | 0.0214591 | intron-variant | GGA2 | GRCh38.p7 | 16:23494256 | CCTCTCGGCTCTCTA[C/G/T]AGCACAAGGACAGGA | 23062 |
rs770872523 | in-del | -/G | 1.64754e-05 | 0.00287009 | frameshift-variant | GGA2 | GRCh38.p7 | 16:23488690 | TCCACTGGTAGTTTA[-/G]GGGTCTTGTTTTATA | 23062 |
rs770959840 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23468302 | CCTGCCTCACTCTCC[C/T]GAGTAGCTGAGACTA | 23062 |
rs771054993 | in-del | -/TG | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465497 | ATGTTCAGGTACACA[-/TG]TGTGAGTTCACCTCC | 23062 |
rs771057782 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23489935 | GAATTATGTCCTGGG[C/T]CCAGATCTACACTGG | 23062 |
rs771058001 | snp | A/G | 6.59044e-05 | 0.00574002 | missense | GGA2 | GRCh38.p7 | 16:23486112 | CGCACTTCCTCCACC[A/G]CACTGACCCTCTTGG | 23062 |
rs771198946 | in-del | -/AG | | | intron-variant | GGA2 | GRCh38.p7 | 16:23469002 | CTCTCATTGACTATC[-/AG]GGGAAGAAAACCAAC | 23062 |
rs771208117 | snp | A/C | 1.6531e-05 | 0.00287493 | intron-variant | GGA2 | GRCh38.p7 | 16:23479754 | TGCTCCCCACAAGCA[A/C]CTGCCCTCACCCAAG | 23062 |
rs771220001 | snp | A/C | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466652 | ACCTCAATCACTGCT[A/C]AGCTCTCTTCATGTC | 23062 |
rs771228903 | snp | A/C | 3.36944e-05 | 0.0041044 | splice-donor-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23495692 | GTGAGAAGTTACCTT[A/C]CCCATTGGGGTCAGT | 23062 |
rs771308624 | snp | G/T | 6.6749e-05 | 0.00577668 | missense | GGA2 | GRCh38.p7 | 16:23478401 | TGTGCTGAGAGGAGG[G/T]CCAGCAAATTCCTGT | 23062 |
rs771342939 | snp | C/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465840 | CAGCTACTCGAGAGG[C/G]TGAGGCACGAGAATC | 23062 |
rs771352039 | snp | A/T | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511713 | CTGTTAAAAGATAAT[A/T]TTCCCAAAAAAGTAT | 23062 |
rs771354194 | snp | A/G | 3.29457e-05 | 0.00405854 | missense | GGA2 | GRCh38.p7 | 16:23486736 | AATTCTTGATTAACC[A/G]GTTTGCAGCCTGAAG | 23062 |
rs771370115 | in-del | -/CTTCTC | | | intron-variant | GGA2 | GRCh38.p7 | 16:23468116 | TTCTTTTCTTTTTCT[-/CTTCTC]CTTCTCCTTCCTTCC | 23062 |
rs771373083 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23473971 | CTCACCACAAAGAGC[C/T]ATAGGAGGGCTCTGT | 23062 |
rs771430125 | snp | C/T | 4.06976e-05 | 0.00451078 | missense | GGA2 | GRCh38.p7 | 16:23467598 | TGAAAAGTTAGGCTG[C/T]GCCCAAGACAGCCAG | 23062 |
rs771433958 | snp | C/T | 1.65296e-05 | 0.00287481 | missense | GGA2 | GRCh38.p7 | 16:23482952 | TCATCAGTGGTGTCA[C/T]TCGCCAACCGGAACA | 23062 |
rs771451056 | in-del | -/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500350 | GGAACATGCTGAGCT[-/G]GTTGCTTGAGCACCA | 23062 |
rs771498767 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23484343 | GAATCGCTCGAACCC[G/T]GGAGGCAGAAGTCGT | 23062 |
rs771518335 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23478020 | CAACATGGTGAAACC[A/C]CGTCTCTACTAAAAA | 23062 |
rs771523810 | snp | A/C | 3.39328e-05 | 0.00411889 | intron-variant | GGA2 | GRCh38.p7 | 16:23478527 | AGGAATGGCTAAAAT[A/C]AGACCAGGGTATGAA | 23062 |
rs771554842 | snp | C/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499909 | GGTGAACCACGTGCC[C/T]AGGCTCCCGCATCAC | 23062 |
rs771574974 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23485407 | GAGCTAGAACTTGCA[C/T]ATGCTGCTGTTAGGA | 23062 |
rs771587955 | snp | A/C | 1.74175e-05 | 0.00295101 | intron-variant | GGA2 | GRCh38.p7 | 16:23478550 | GGTATGAATGACCAT[A/C]AGCCACAGTAAAACC | 23062 |
rs771608334 | in-del | -/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23491874 | TAACTAAAGAGGTAG[-/C]CTGCTGAGGCCCAGA | 23062 |
rs771609957 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23498865 | AGCAGTGATTCTCAG[A/C]GATTATGTGTCTGAA | 23062 |
rs771625956 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23498624 | CATGGGACTGTCATG[C/T]GATTTAAAGGGGAAG | 23062 |
rs771678083 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23508885 | GGCATCTGTAACCCA[C/T]CAGTTCCTCGAGCCT | 23062 |
rs771736017 | snp | A/G | 1.65094e-05 | 0.00287305 | intron-variant | GGA2 | GRCh38.p7 | 16:23493341 | GACACAGTCAGCAGA[A/G]CCAAGCCCAGGTACT | 23062 |
rs771792880 | snp | A/C/G | 3.31166e-05 | 0.00406908 | intron-variant | GGA2 | GRCh38.p7 | 16:23491803 | AGGACCCCAGGTACT[A/C/G]AAAGTAAAAAGGAAA | 23062 |
rs771802358 | snp | A/G | 1.85221e-05 | 0.00304314 | intron-variant | GGA2 | GRCh38.p7 | 16:23470216 | ACTACAAACCCCCCG[A/G]ACAGCCAGGCTGGAA | 23062 |
rs771872938 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | GGA2 | GRCh38.p7 | 16:23486714 | AGAATGCCCACCTCC[C/T]TGACCAAATTCTTGA | 23062 |
rs771949590 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23492799 | TGAGGACACATGAGA[C/T]TCACGGCTGGCAGCT | 23062 |
rs771964803 | snp | C/T | 1.69873e-05 | 0.00291434 | intron-variant | GGA2 | GRCh38.p7 | 16:23479031 | CAAATAAGCAACTTA[C/T]TGAAGGTCATGTGAC | 23062 |
rs772000231 | snp | C/T | 1.65652e-05 | 0.0028779 | missense | GGA2 | GRCh38.p7 | 16:23470102 | CCAGGGGCTCCCGTC[C/T]GGGAGAAGTGGAGCA | 23062 |
rs772057343 | in-del | -/TCC | 4.96874e-05 | 0.0049841 | intron-variant | GGA2 | GRCh38.p7 | 16:23479729 | CCCTACTCGCACCCA[-/TCC]TCCTGTGCCTGCTCC | 23062 |
rs772108972 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23480257 | AGCTCCAAGCAGTCT[G/T]GATTCAGAAGGTCCA | 23062 |
rs772125183 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23493564 | TGGAACCAAGGCTAA[C/G]CCTGCCTCAAGCCTA | 23062 |
rs772162595 | snp | C/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501265 | AACTAATGGTAGCAT[C/T]GCTCTGTGTCCTACT | 23062 |
rs772202191 | snp | A/C/G | 3.54687e-05 | 0.0042111 | intron-variant | GGA2 | GRCh38.p7 | 16:23475079 | ACAAAGAAATAAAAA[A/C/G]TATCAAAGACTAGCA | 23062 |
rs772272620 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23489755 | AAGAAAATAAGCTCT[C/T]CTCCAGAGGCTCACG | 23062 |
rs772323794 | snp | A/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23488428 | ACTGGCCCTTATTAG[A/T]TGACTTATCCATGAA | 23062 |
rs772335526 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23469912 | GAAGATTCTTTCCTT[A/G]ACACTCGACAGGTAA | 23062 |
rs772380114 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23478952 | GCCTAACAGTAACTC[C/T]ACCTGCTTCCAGATG | 23062 |
rs772412862 | snp | A/T | 1.64776e-05 | 0.00287028 | intron-variant | GGA2 | GRCh38.p7 | 16:23486834 | GAGACCACAACTCCC[A/T]CAGGCCTAGAGCAGA | 23062 |
rs772439310 | snp | A/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464710 | CTCAGGTGCTTTCAA[A/G]TAAGAGCATGTAGGT | 23062 |
rs772474223 | in-del | -/AAAAA | | | intron-variant | GGA2 | GRCh38.p7 | 16:23495080 | CACTCTGTCTCAGGA[-/AAAAA]AAAAAAAGAAAAGAA | 23062 |
rs772497626 | snp | A/G | 0.000155099 | 0.00880485 | intron-variant | GGA2 | GRCh38.p7 | 16:23510270 | GGAGGCGGGAAGCGA[A/G]GCCTCACGTGCGGCG | 23062 |
rs772524455 | in-del | -/TC | | | utr-variant-3-prime, downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23464117 | CTAGCTTTAACATTT[-/TC]TGTCTCAATTTACAC | 23062 |
rs772531183 | snp | A/G | 0.000162448 | 0.00901096 | intron-variant | GGA2 | GRCh38.p7 | 16:23478641 | GGGCAAGAGGGGAAA[A/G]AAAGGGCAAGATCAC | 23062 |
rs772681875 | snp | C/T | 1.7238e-05 | 0.00293576 | missense | GGA2 | GRCh38.p7 | 16:23467684 | AATGTCAGCTTGTAC[C/T]GTAAGCGGATAGGTT | 23062 |
rs772691810 | snp | C/G | 1.65411e-05 | 0.00287581 | missense, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23495737 | AGAAATTCTGGATAG[C/G]TGACCAATCCTGTTC | 23062 |
rs772702107 | snp | A/C | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511394 | TCGAACTCCTGACCT[A/C]GTGATCTGCCCGCTT | 23062 |
rs772718680 | snp | C/T | 1.79803e-05 | 0.0029983 | intron-variant | GGA2 | GRCh38.p7 | 16:23469949 | GAAAAGAACCTGGCA[C/T]TCAAAAACGACAGCC | 23062 |
rs772719250 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23478365 | CTTGCCCAGAAGACT[C/T]ACAGAGGGCACGGAG | 23062 |
rs772738100 | snp | C/G | 1.65652e-05 | 0.0028779 | missense | GGA2 | GRCh38.p7 | 16:23468930 | GAGATATCACAGCTG[C/G]AGGCATCAAAGGACT | 23062 |
rs772745327 | snp | C/T | 9.88338e-05 | 0.00702902 | missense | GGA2 | GRCh38.p7 | 16:23491704 | GCATCTGATAAGCGT[C/T]TCGAATCTTGATGTC | 23062 |
rs772751597 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23481370 | AAGAGCGAAACTCCA[C/T]CTCAAGAAAAAAAGA | 23062 |
rs772755351 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23508935 | AGATTTCTCCTTGTC[C/T]CCTGTCTGCATTCCA | 23062 |
rs772790400 | snp | C/T | | | utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23510441 | CGCTGCGGCCGCGGG[C/T]GCCACTGCCTCTTCA | 23062 |
rs772799908 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23472892 | ACAAAAAAGTAGCTG[G/T]GCGTGGTTGTGGGCA | 23062 |
rs772835267 | snp | C/T | 1.64852e-05 | 0.00287094 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23480682 | CAATGAGCTGGTCAC[C/T]CTGTTTCCAAAGGTG | 23062 |
rs772879254 | in-del | -/G | 1.6476e-05 | 0.00287014 | intron-variant | GGA2 | GRCh38.p7 | 16:23474863 | TCTAATAGATTCCCA[-/G]GGGAAAAAAAAAAAA | 23062 |
rs772948006 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23491993 | CAAGGAATTCATCTC[A/G]GCAATACTCACACTA | 23062 |
rs772970942 | in-del | -/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23481154 | GAGGCCGAGGCGGGT[-/G]GATCACCTGAGGTCA | 23062 |
rs773020238 | snp | C/G | 0.000121245 | 0.00778509 | intron-variant | GGA2 | GRCh38.p7 | 16:23478707 | CCTGGTGCAACCTGT[C/G]TCCCCCAGGTATCAG | 23062 |
rs773061432 | in-del | -/TTT | | | intron-variant | GGA2 | GRCh38.p7 | 16:23470826 | AAATGAAATAAATGC[-/TTT]TTTTTTTTTTTTTTT | 23062 |
rs773061788 | snp | C/T | 0.000248973 | 0.0111546 | synonymous-codon, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23510352 | CGACGCTGCCGGGCC[C/T]GGGGGACCCTGGGCC | 23062 |
rs773097267 | snp | A/G | 1.64953e-05 | 0.00287182 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23486033 | CAGGGCCTCCTGGTC[A/G]GGCGGGGCCTGCCCT | 23062 |
rs773150787 | snp | A/G | | | missense | GGA2 | GRCh38.p7 | 16:23488634 | TCATCAGCATCAAAG[A/G]TGGAGCTCTTGGGCC | 23062 |
rs773213353 | snp | C/T | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467080 | GAGACAAGGTCTTTC[C/T]TGGAAGAGAGTGCCC | 23062 |
rs773228031 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23481575 | CCCAGGAGTTTGAGA[A/C]CAGCCTGGCCAACAT | 23062 |
rs773229216 | snp | A/G | 0.000397472 | 0.0140918 | intron-variant | GGA2 | GRCh38.p7 | 16:23479037 | AGCAACTTACTGAAG[A/G]TCATGTGACTCGTCC | 23062 |
rs773239287 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23491137 | GGGGTGTGGGTGGGA[A/G]AATAATAATAAATGA | 23062 |
rs773253620 | in-del | -/GAAGA | 1.69971e-05 | 0.00291518 | intron-variant | GGA2 | GRCh38.p7 | 16:23479907 | AAAGCCCAGGGTTAG[-/GAAGA]GAAGTCAGTTGGACA | 23062 |
rs773258066 | snp | A/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23488436 | TTATTAGTTGACTTA[A/T]CCATGAAGAACGCAC | 23062 |
rs773293701 | snp | G/T | 2.70896e-05 | 0.00368023 | intron-variant | GGA2 | GRCh38.p7 | 16:23493525 | CTCCCCTCCAGGCTG[G/T]TAATCACTTGCTGGA | 23062 |
rs773323511 | snp | C/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23502438 | CTTCCAGGAAAACAA[C/T]AAAAGAGGAACATCT | 23062 |
rs773353211 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23480407 | AGAATTCAAACGCAG[A/G]CACAGCTTAGCCATC | 23062 |
rs773366934 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23477724 | TGCACTCCACCCAGG[A/G]CGACAGAGCGAGACT | 23062 |
rs773420855 | snp | C/T | 3.29587e-05 | 0.00405934 | intron-variant | GGA2 | GRCh38.p7 | 16:23494281 | ACAGGAAAGGTTAGG[C/T]TACAAGGCAAGCCAA | 23062 |
rs773428937 | in-del | -/AA | 4.96208e-05 | 0.00498076 | intron-variant | GGA2 | GRCh38.p7 | 16:23494391 | GGGCTACAGGGAAAC[-/AA]AAAGACCTAGACTCT | 23062 |
rs773491406 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23489766 | CTCTTCTCCAGAGGC[C/T]CACGAAAACAGCGGG | 23062 |
rs773493534 | snp | A/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23477020 | GCAGTGGCATAGTAA[A/T]GGCTCACTGCAGCCT | 23062 |
rs773628395 | snp | A/G | 1.6549e-05 | 0.0028765 | intron-variant | GGA2 | GRCh38.p7 | 16:23486168 | CTTTTGGGAAAAAGA[A/G]GAGGATGGGAGTGAG | 23062 |
rs773667273 | in-del | -/A | | | intron-variant | GGA2 | GRCh38.p7 | 16:23486468 | CCCAAGCTGGTGTCT[-/A]AGGAAATGCTTTGAG | 23062 |
rs773687384 | snp | C/T | 1.65056e-05 | 0.00287272 | synonymous-codon, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23494357 | GATCTTGTGGGCCAG[C/T]AGCCAGGGCGCATGT | 23062 |
rs773733961 | in-del | -/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23485918 | GATATGTTTACCGTC[-/T]TTGACTCTGAGATGG | 23062 |
rs773808073 | snp | C/T | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465833 | GTAGTCCCAGCTACT[C/T]GAGAGGCTGAGGCAC | 23062 |
rs773808118 | snp | A/G/T | 8.3953e-05 | 0.00647845 | intron-variant | GGA2 | GRCh38.p7 | 16:23482872 | TGACAGGAGGGACCG[A/G/T]GTCTGTCTTGCACCT | 23062 |
rs773814797 | snp | A/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499065 | AGGAGGCATGGCCCA[A/G]GCTCCCCTCACAGAA | 23062 |
rs773859373 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23504937 | TGAAATGGCTCATCC[A/G]AGAGTGACTAATTCA | 23062 |
rs773922811 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23471702 | GTCAGGAGTTCAAAA[C/G]CAGCCTGGGCAATAC | 23062 |
rs773959007 | snp | A/T | 0.000133427 | 0.00816674 | missense | GGA2 | GRCh38.p7 | 16:23478404 | GCTGAGAGGAGGTCC[A/T]GCAAATTCCTGTCTG | 23062 |
rs774004320 | snp | C/T | 4.94523e-05 | 0.00497229 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23491780 | TCCTTTAACTTTTCC[C/T]GTGGCCCAGGACCCC | 23062 |
rs774045200 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23483805 | GGCATGCGCCACCAC[A/G]CCCGGCTGATACTGT | 23062 |
rs774059505 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23470415 | GTTATTAAAAATCAC[A/G]TTTTTGAGGAAGATA | 23062 |
rs774102747 | snp | C/G | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23502909 | ACAAGAACACCAGAT[C/G]CCCACCAATGTGAGA | 23062 |
rs774116316 | in-del | -/G | 1.65353e-05 | 0.00287531 | frameshift-variant | GGA2 | GRCh38.p7 | 16:23491797 | TGGCCCAGGACCCCA[-/G]GTACTGAAAGTAAAA | 23062 |
rs774194384 | snp | A/G | 9.88338e-05 | 0.00702902 | stop-gained | GGA2 | GRCh38.p7 | 16:23491707 | TCTGATAAGCGTCTC[A/G]AATCTTGATGTCTTC | 23062 |
rs774236035 | snp | C/T | 1.66757e-05 | 0.00288749 | missense | GGA2 | GRCh38.p7 | 16:23478905 | GTAACAGGAGCATCA[C/T]TGATTCCTGTAAGAA | 23062 |
rs774242311 | snp | A/G | 1.65638e-05 | 0.00287778 | missense | GGA2 | GRCh38.p7 | 16:23468942 | CTGGAGGCATCAAAG[A/G]ACTGAATGCAGGAAG | 23062 |
rs774262456 | snp | C/T | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504005 | AGAATTGCTTGAACC[C/T]GGGAGACGGAGGTTG | 23062 |
rs774314067 | snp | A/G | | | missense | GGA2 | GRCh38.p7 | 16:23470151 | GGTCATACACAATGA[A/G]AGGCGGCAGGCTGCC | 23062 |
rs774323871 | snp | A/G | 5.36658e-05 | 0.00517977 | intron-variant | GGA2 | GRCh38.p7 | 16:23469971 | ACGACAGCCATTACT[A/G]AGAAATCCCCAACAG | 23062 |
rs774375725 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23488362 | CACAAACAGATCCTA[C/G]CAAGACCCAGGATGC | 23062 |
rs774432373 | snp | C/G | 2.04987e-05 | 0.0032014 | intron-variant | GGA2 | GRCh38.p7 | 16:23478807 | CACCTCTCTGCTCGC[C/G]AGGCAGTGCTGCCTC | 23062 |
rs774451751 | snp | A/G | 1.64798e-05 | 0.00287047 | missense | GGA2 | GRCh38.p7 | 16:23474946 | ACACTTGAGCCAGAG[A/G]TGTATTCTGTGAAGA | 23062 |
rs774544339 | snp | A/G | 1.6473e-05 | 0.00286988 | missense | GGA2 | GRCh38.p7 | 16:23486744 | ATTAACCGGTTTGCA[A/G]CCTGAAGGTCCTCGG | 23062 |
rs774557395 | snp | C/G | 1.65269e-05 | 0.00287457 | intron-variant | GGA2 | GRCh38.p7 | 16:23479757 | TCCCCACAAGCACCT[C/G]CCCTCACCCAAGGCT | 23062 |
rs774562571 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23506571 | GAGCTTTGGTATCCA[C/G]TGGATTTAGCCCAGG | 23062 |
rs774580784 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23495195 | CAGAATTCAATAAAA[C/T]CTTCCCCTTTTCCTT | 23062 |
rs774591942 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23468227 | TCTGTCACCAGGCTG[G/T]AGTGCAGTGGTGCGA | 23062 |
rs774605658 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23476634 | AGGTCATGCTGGAGT[A/G]CGGTTTATAAATTAA | 23062 |
rs774620848 | snp | C/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501194 | TACTCTTTTTCAAGT[C/T]ATAAAACTACAGCTC | 23062 |
rs774636808 | snp | A/C | 1.66098e-05 | 0.00288177 | intron-variant | GGA2 | GRCh38.p7 | 16:23493464 | TCTCCAGCACCTGCA[A/C]AGACACAGGACCCCC | 23062 |
rs774699061 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23487228 | CTCGTGATCCACCCA[C/T]CTCGGCCTCCCAAAA | 23062 |
rs774711955 | snp | A/G | 1.71237e-05 | 0.00292602 | intron-variant | GGA2 | GRCh38.p7 | 16:23478538 | AAATAAGACCAGGGT[A/G]TGAATGACCATCAGC | 23062 |
rs774743881 | snp | C/T | 0.000116377 | 0.00762724 | missense, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23495707 | ACCCATTGGGGTCAG[C/T]GTTCACCTGCTCACA | 23062 |
rs774755573 | snp | C/T | 2.02251e-05 | 0.00317996 | intron-variant | GGA2 | GRCh38.p7 | 16:23479072 | CCAATCTGTGACTAA[C/T]ATGCAAGGGGGACCC | 23062 |
rs774832157 | snp | A/G | 1.64749e-05 | 0.00287005 | intron-variant | GGA2 | GRCh38.p7 | 16:23486817 | GAACAGGAAGAGTAG[A/G]TGAGACCACAACTCC | 23062 |
rs774839162 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23497972 | GACCCAATCTCCACA[A/G]AAATTTTTAAAAAAA | 23062 |
rs774868731 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23495385 | TGTTTTTTTTCCCCC[A/G]CATGAATTTGCTAAT | 23062 |
rs774935798 | snp | A/G | 3.49424e-05 | 0.00417971 | intron-variant | GGA2 | GRCh38.p7 | 16:23478551 | GTATGAATGACCATC[A/G]GCCACAGTAAAACCA | 23062 |
rs774937141 | snp | C/T | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464467 | ATTCAGAATTTTTCA[C/T]CCTGTCAGATGCTCA | 23062 |
rs774956253 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23493888 | ACTGTGGCTTTCAAC[A/G]CTGCAAATTAGTCAC | 23062 |
rs774983371 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23477601 | AAATACAAAAAATTA[A/G]CCGGGTGTGGTGGCA | 23062 |
rs775023680 | snp | C/T | 8.25389e-05 | 0.0064236 | intron-variant | GGA2 | GRCh38.p7 | 16:23478663 | CAAGATCACATGCAG[C/T]TCCTGGGCAGACCTC | 23062 |
rs775081412 | in-del | -/GT | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510872 | CACCACGCCTGGCGT[-/GT]GTGTGTGTGTGTGTG | 23062 |
rs775115194 | snp | A/G | 1.65288e-05 | 0.00287474 | intron-variant | GGA2 | GRCh38.p7 | 16:23494384 | ATGTGTGGGGCTACA[A/G]GGAAACAAAAAGACC | 23062 |
rs775189132 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23494957 | AGGCATGGAGGCACG[C/T]GCCTGTAATCCCAGC | 23062 |
rs775189262 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23481816 | GAGGGCATGCACATG[C/T]TATCCACTAAGAGAG | 23062 |
rs775243288 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23490045 | AGACTGGCCCTGCCC[A/G]CCACCCTATCCCTCT | 23062 |
rs775297093 | snp | A/G | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23502670 | AGCAGCGGTTCTCAC[A/G]GGAGCAGCTTCTGCA | 23062 |
rs775321784 | in-del | -/G | 1.75136e-05 | 0.00295914 | intron-variant | GGA2 | GRCh38.p7 | 16:23470176 | GCTGCCTGGTATAAA[-/G]GGCACAAGCAGAAGG | 23062 |
rs775324541 | snp | A/G | 1.67775e-05 | 0.00289629 | intron-variant | GGA2 | GRCh38.p7 | 16:23482882 | GACCGAGTCTGTCTT[A/G]CACCTGGGCTGCTAG | 23062 |
rs775331717 | snp | A/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23471448 | CTCAGATAAAATTAC[A/T]ATTCAAGTAAAGTGA | 23062 |
rs775368972 | snp | G/T | 1.66021e-05 | 0.0028811 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23470113 | CGTCTGGGAGAAGTG[G/T]AGCAGAATTCTGAAT | 23062 |
rs775378268 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23470195 | ACAAGCAGAAGGTTT[A/G]ACACCACTACAAACC | 23062 |
rs775399105 | snp | C/T | 0.000275022 | 0.0117233 | intron-variant | GGA2 | GRCh38.p7 | 16:23493543 | ATCACTTGCTGGAGA[C/T]TGCGCTGGAACCAAG | 23062 |
rs775405675 | in-del | -/TTGT | | | intron-variant | GGA2 | GRCh38.p7 | 16:23483639 | GTGGTTTCTTTTTGA[-/TTGT]TTGTTTTTTTGGTTT | 23062 |
rs775415753 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23485500 | TATATACTTAGCATA[C/T]GACCTAGTAATCCCA | 23062 |
rs775489102 | snp | A/G | 3.2975e-05 | 0.00406035 | missense | GGA2 | GRCh38.p7 | 16:23486037 | GCCTCCTGGTCGGGC[A/G]GGGCCTGCCCTGGCC | 23062 |
rs775521990 | snp | G/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500058 | AGGAGCTCCCTCTGT[G/T]CTCTCTTCTCCGCAA | 23062 |
rs775547134 | snp | C/T | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465868 | ATCGCTTGAACCTGG[C/T]AGGCAGAGATTGCAG | 23062 |
rs775567103 | snp | C/G | 0.000158614 | 0.00890404 | missense | GGA2 | GRCh38.p7 | 16:23469996 | CAACAGATGACTCAC[C/G]TTTGGCACAGCCACT | 23062 |
rs775610615 | in-del | -/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23477713 | GATCGCGCCACTGCA[-/C]TCCACCCAGGGCGAC | 23062 |
rs775668242 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23480151 | GGAGGAAAGCAGATT[C/T]GGCCTTCTCCAGCTC | 23062 |
rs775762844 | snp | A/G | 0.000462504 | 0.0151999 | intron-variant | GGA2 | GRCh38.p7 | 16:23474887 | AAAAAAAAGGTGGGG[A/G]GTGAAATTGTACTTA | 23062 |
rs775782814 | snp | A/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499336 | TTTTCAGTAGAGATG[A/G]GGTTTCACTATATTG | 23062 |
rs775803198 | snp | C/T | 1.68196e-05 | 0.00289992 | intron-variant | GGA2 | GRCh38.p7 | 16:23493476 | GCACAGACACAGGAC[C/T]CCCAGGAGAAGGTGG | 23062 |
rs775844878 | snp | A/G/T | 3.45276e-05 | 0.00415485 | synonymous-codon, missense | GGA2 | GRCh38.p7 | 16:23467685 | ATGTCAGCTTGTACC[A/G/T]TAAGCGGATAGGTTC | 23062 |
rs775921031 | in-del | -/TT/TTT/TTTT | | | intron-variant | GGA2 | GRCh38.p7 | 16:23486984 | TTTTCTTTTCTGTTG[-/TT/TTT/TTTT]TTTTTTTTTTTTTTT | 23062 |
rs775930231 | in-del | -/TC | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511154 | TTTATTTTTTATTTT[-/TC]TTTTTTTCTTTTTTT | 23062 |
rs775975158 | snp | C/T | 1.66696e-05 | 0.00288696 | missense | GGA2 | GRCh38.p7 | 16:23479878 | ATGCAGCCTGCTGGA[C/T]TCTGAAAGACTAGAA | 23062 |
rs776036665 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23474827 | GCCACCTCTATCAAA[C/G]TGGAGTGGAAAAAGC | 23062 |
rs776070284 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23476460 | CAGGGATCTATACTA[C/T]AAGGCACTCCCCCAA | 23062 |
rs776155723 | snp | C/T | 0.000820232 | 0.0202347 | intron-variant | GGA2 | GRCh38.p7 | 16:23510272 | AGGCGGGAAGCGAGG[C/T]CTCACGTGCGGCGCA | 23062 |
rs776158618 | snp | G/T | 1.65798e-05 | 0.00287917 | missense | GGA2 | GRCh38.p7 | 16:23468893 | GAACATACTTTGTGT[G/T]GATTGTCAAGCAGCA | 23062 |
rs776171544 | snp | C/T | 1.65894e-05 | 0.00288 | missense, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23495758 | AATCCTGTTCCGACA[C/T]GCTTGGGTCTGTGGC | 23062 |
rs776177345 | snp | A/C/G | 0.000677787 | 0.0183987 | missense, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23510327 | GCTACTCACTGAGCC[A/C/G]CAGCTCCAGCGACGC | 23062 |
rs776218406 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23485020 | TGGAGAAACAAACTG[C/T]GGCATAGCCACACAA | 23062 |
rs776234618 | in-del | -/CACT | 1.80201e-05 | 0.00300162 | intron-variant | GGA2 | GRCh38.p7 | 16:23470199 | CAGAAGGTTTAACAC[-/CACT]CACTACAAACCCCCC | 23062 |
rs776274075 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23505929 | ACTTTCTTTACTTTC[C/T]TTTTTTTGGTAAGCG | 23062 |
rs776341701 | snp | C/T | 3.40327e-05 | 0.00412495 | intron-variant | GGA2 | GRCh38.p7 | 16:23483014 | CACGACCTGAAAGAG[C/T]AGAGCTTGGTTCATG | 23062 |
rs776464589 | in-del | -/TTGCACCTGGG | | | intron-variant | GGA2 | GRCh38.p7 | 16:23482869 | TGTGACAGGAGGGAC[-/TTGCACCTGGG]CGAGTCTGTCTTGCA | 23062 |
rs776489445 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23509393 | CTGTGACGACCCCCA[A/G]GTAAACCAACTCCTA | 23062 |
rs776490970 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23482554 | CTCTTAGTTGACCTA[C/T]CTGGCCCCTGAAGGT | 23062 |
rs776529428 | snp | C/T | 1.65184e-05 | 0.00287384 | missense | GGA2 | GRCh38.p7 | 16:23493447 | ACAGTGGTTCATGCA[C/T]ATCTCCAGCACCTGC | 23062 |
rs776534413 | snp | A/T | 1.64836e-05 | 0.0028708 | missense | GGA2 | GRCh38.p7 | 16:23486136 | CTCTTGGACACCTTC[A/T]CCGATTTTTCTTGTT | 23062 |
rs776540969 | snp | C/T | 1.99289e-05 | 0.00315659 | intron-variant | GGA2 | GRCh38.p7 | 16:23478576 | AAACCAAGGCACAGC[C/T]CTCCTGAGCCCACCC | 23062 |
rs776575076 | in-del | -/AA | | | intron-variant | GGA2 | GRCh38.p7 | 16:23498756 | TGTCTTGTCCTACCT[-/AA]AGAGAATGAAACCTT | 23062 |
rs776602457 | in-del | -/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23471450 | CAGATAAAATTACAA[-/T]TCAAGTAAAGTGACA | 23062 |
rs776625169 | snp | C/G | 3.33172e-05 | 0.00408136 | intron-variant | GGA2 | GRCh38.p7 | 16:23474865 | CTAATAGATTCCCAG[C/G]GAAAAAAAAAAAAAG | 23062 |
rs776626780 | snp | A/G | 1.71346e-05 | 0.00292694 | intron-variant | GGA2 | GRCh38.p7 | 16:23478937 | GGAGTAGAGTGAGAT[A/G]CCTAACAGTAACTCC | 23062 |
rs776681718 | snp | A/C | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511723 | ATAATTTTCCCAAAA[A/C]AGTATGTCATGATTA | 23062 |
rs776697581 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23491452 | TTTCCAGGCAACAGG[A/G]AAAAAAGCAAACCCT | 23062 |
rs776727179 | snp | C/G | 1.64898e-05 | 0.00287135 | splice-donor-variant | GGA2 | GRCh38.p7 | 16:23493359 | AAGCCCAGGTACTCA[C/G]CTTTGGGGACAACAC | 23062 |
rs776739810 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23491401 | TGACATAGGTAGCTT[A/G]TATTTTGACCTTTTT | 23062 |
rs776777256 | snp | C/T | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465848 | CGAGAGGCTGAGGCA[C/T]GAGAATCGCTTGAAC | 23062 |
rs776814383 | snp | A/G | 1.64803e-05 | 0.00287052 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23474971 | TGAAGATGGGGAAGG[A/G]GCCAACGGGCCAGCC | 23062 |
rs776853556 | snp | G/T | 1.64817e-05 | 0.00287064 | intron-variant | GGA2 | GRCh38.p7 | 16:23494275 | ACAAGGACAGGAAAG[G/T]TTAGGCTACAAGGCA | 23062 |
rs776956829 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23497764 | TATCTGCCCCTTCTC[C/T]GATAGGGATCTCCAG | 23062 |
rs776969497 | snp | C/T | 0.000260451 | 0.0114087 | intron-variant | GGA2 | GRCh38.p7 | 16:23479076 | TCTGTGACTAATATG[C/T]AAGGGGGACCCTCTG | 23062 |
rs777047654 | snp | C/T | 0.000137121 | 0.00827899 | intron-variant | GGA2 | GRCh38.p7 | 16:23493549 | TGCTGGAGACTGCGC[C/T]GGAACCAAGGCTAAC | 23062 |
rs777087598 | snp | A/G | 1.65059e-05 | 0.00287275 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23480652 | AAACATACCTCTGGA[A/G]ACAGGGATGTCTCCC | 23062 |
rs777175077 | snp | C/T | 8.28878e-05 | 0.00643716 | missense | GGA2 | GRCh38.p7 | 16:23470055 | GAGCCGTGCTCATCA[C/T]GGTCAAGAGCAGCAC | 23062 |
rs777181152 | in-del | -/AGAAG | 1.64738e-05 | 0.00286995 | frameshift-variant | GGA2 | GRCh38.p7 | 16:23486774 | GGGTGGTTGCTCTTT[-/AGAAG]CCTTGTCAGAAGCTG | 23062 |
rs777203576 | snp | A/T | 1.64741e-05 | 0.00286998 | missense | GGA2 | GRCh38.p7 | 16:23491762 | GAGTATTTCAATGAC[A/T]CTTCCTTTAACTTTT | 23062 |
rs777222210 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23486512 | AGCAGCTGAGAAGTA[C/T]GGCAGCGGGATTTCT | 23062 |
rs777225953 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23487885 | AACGAGTACGCAGCG[C/T]GTAGCCTTCCAACAC | 23062 |
rs777285762 | snp | A/C | 0.00011816 | 0.00768546 | intron-variant | GGA2 | GRCh38.p7 | 16:23479896 | TGAAAGACTAGAAAG[A/C]CCAGGGTTAGGAAGA | 23062 |
rs777343250 | snp | G/T | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467325 | AGATGATGATGATGA[G/T]AAATGCTTCGCATTT | 23062 |
rs777346913 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23485714 | CACAGCAACGTGAAT[A/G]GATCTCGAGTGAGAT | 23062 |
rs777349366 | in-del | -/GTGTGTGTGTGTGTGTGTGTGT | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510907 | AGACTGGGTTTCACC[-/GTGTGTGTGTGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 23062 |
rs777410429 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23505598 | AACGGCTTCCTGATA[C/T]TCCTCTGGGAACAAC | 23062 |
rs777419458 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23474732 | GCTGGGATTACAGGC[A/G]TGAGTCACCATACCT | 23062 |
rs777450301 | in-del | -/C | 0.00318108 | 0.0397545 | intron-variant | GGA2 | GRCh38.p7 | 16:23493474 | TGCACAGACACAGGA[-/C]CCCCCAGGAGAAGGT | 23062 |
rs777480628 | snp | C/T | 0.00010785 | 0.00734256 | intron-variant | GGA2 | GRCh38.p7 | 16:23478345 | AGCCACACTCTCCCA[C/T]TCCCCTTGCCCAGAA | 23062 |
rs777532634 | snp | A/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464408 | GCACTGAGTGCCAGC[A/G]TGCAACTTGAATTTG | 23062 |
rs777561825 | snp | G/T | 1.6476e-05 | 0.00287014 | intron-variant | GGA2 | GRCh38.p7 | 16:23486677 | GCCTCTGTCAAATGC[G/T]ACTTCTACTGAACCA | 23062 |
rs777629237 | snp | C/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500880 | TTTTTTGAGAAAATA[C/T]CAAATGAGTGTGCAA | 23062 |
rs777642356 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23493596 | GAGGACACTGAAGTT[C/T]TGATGAAGAGGACGT | 23062 |
rs777670618 | snp | A/G | 3.4856e-05 | 0.00417454 | intron-variant | GGA2 | GRCh38.p7 | 16:23475067 | AACATAATTCCTACA[A/G]AGAAATAAAAAATAT | 23062 |
rs777671308 | snp | C/T | 1.64866e-05 | 0.00287106 | missense, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23494326 | CATAAAGAGCTTCCT[C/T]CTCTTGCGGAGACTG | 23062 |
rs777736635 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23484635 | TGAGCATAGGAAATA[A/C]ATAAGCCATCAAGAA | 23062 |
rs777759899 | snp | A/G | 4.9423e-05 | 0.00497082 | missense | GGA2 | GRCh38.p7 | 16:23486100 | TTCACATGGCTTCGC[A/G]CTTCCTCCACCGCAC | 23062 |
rs777834866 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23507023 | AAGAGGGGCTCACAT[C/G]TCCCCCTCTCCTTCT | 23062 |
rs777854676 | in-del | -/G | 3.04586e-05 | 0.00390235 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467559 | GTAACGCCAGCCTAA[-/G]CTTGAAATGAAGGGT | 23062 |
rs777867432 | snp | A/G | 1.71613e-05 | 0.00292923 | intron-variant | GGA2 | GRCh38.p7 | 16:23495677 | GAGTCAACTATGTGT[A/G]TGAGAAGTTACCTTA | 23062 |
rs777876759 | snp | A/T | 1.6473e-05 | 0.00286988 | missense | GGA2 | GRCh38.p7 | 16:23488650 | TGGAGCTCTTGGGCC[A/T]GGGAGATGGTGGGGG | 23062 |
rs777928906 | snp | C/T | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503692 | CCCTGCACTTTAGCT[C/T]CACTGCATACTGAAT | 23062 |
rs777935824 | snp | A/T | 1.71117e-05 | 0.00292499 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23467656 | TTCGCTGAAAGGCTG[A/T]CCACCTTGGTTGAAT | 23062 |
rs778030821 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23471175 | CCAGAAATAAGCACT[C/T]ACTTCCTTCTGGTCT | 23062 |
rs778086819 | in-del | -/TTT | | | intron-variant | GGA2 | GRCh38.p7 | 16:23473673 | GAACATGTATTTTTG[-/TTT]TTAACTTTTTTATTT | 23062 |
rs778124892 | snp | A/G | 3.78594e-05 | 0.00435066 | intron-variant | GGA2 | GRCh38.p7 | 16:23478628 | GTGACATCTCTTGGG[A/G]CAAGAGGGGAAAGAA | 23062 |
rs778130677 | snp | C/T | 5.21254e-05 | 0.0051049 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467575 | CTTGAAATGAAGGGT[C/T]CATCTTGTGAAAAGT | 23062 |
rs778143675 | snp | A/G | 1.92907e-05 | 0.00310564 | intron-variant | GGA2 | GRCh38.p7 | 16:23478964 | CTCCACCTGCTTCCA[A/G]ATGAAGAGTAATGCC | 23062 |
rs778143804 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23492582 | AGAGTCCAGGGGAGG[A/G]CACAGCAGCTCTGTC | 23062 |
rs778179935 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23472066 | ATCAAAATTTTAAAT[A/G]TCTACATGTGGCATT | 23062 |
rs778316601 | snp | A/G | 1.80185e-05 | 0.00300149 | intron-variant | GGA2 | GRCh38.p7 | 16:23470201 | AGAAGGTTTAACACC[A/G]CTACAAACCCCCCGG | 23062 |
rs778321014 | snp | C/G | 1.69275e-05 | 0.0029092 | intron-variant | GGA2 | GRCh38.p7 | 16:23478519 | GTCAAATCAGGAATG[C/G]CTAAAATAAGACCAG | 23062 |
rs778352250 | snp | C/G | 1.6531e-05 | 0.00287493 | intron-variant | GGA2 | GRCh38.p7 | 16:23493330 | GGCGTAGGTGCGACA[C/G]AGTCAGCAGAGCCAA | 23062 |
rs778373151 | snp | C/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499737 | AAAGTGTTAGGATTA[C/T]AGATGTGAGCCACTG | 23062 |
rs778455162 | snp | G/T | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510733 | TTTTTAAGAGACGGG[G/T]TCTTGCTCTGTCACT | 23062 |
rs778507269 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463827 | GCAACATTAGCTGGG[C/T]GTGGCAGCATGCACC | 23062 |
rs778508745 | snp | A/G | 3.31098e-05 | 0.00406864 | intron-variant | GGA2 | GRCh38.p7 | 16:23479740 | ACCCATCCTGTGCCT[A/G]CTCCCCACAAGCACC | 23062 |
rs778524604 | snp | A/G | 3.29478e-05 | 0.00405867 | intron-variant | GGA2 | GRCh38.p7 | 16:23486693 | ACTTCTACTGAACCA[A/G]CTGGAAGAATGCCCA | 23062 |
rs778565444 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23491044 | ACAAAAAATACAAAT[A/G]TTTGGTGTAAGTGAG | 23062 |
rs778674172 | snp | A/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466290 | CTCAGCCAGGCTCAG[A/G]TTCCTTCTCCCACCC | 23062 |
rs778695935 | snp | A/G | 1.66969e-05 | 0.00288932 | missense | GGA2 | GRCh38.p7 | 16:23478461 | GGCAGCGTGCTGGAG[A/G]AGGGATTCCTCTTTT | 23062 |
rs778696466 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23498423 | ACAAAATGAGACCCC[A/G]TCTCAAAAATAATAA | 23062 |
rs778698998 | snp | C/G | 3.31076e-05 | 0.0040685 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23470098 | GTGCCCAGGGGCTCC[C/G]GTCTGGGAGAAGTGG | 23062 |
rs778699196 | snp | A/G | 3.31956e-05 | 0.0040739 | intron-variant | GGA2 | GRCh38.p7 | 16:23479723 | CTCACTCCCCTACTC[A/G]CACCCATCCTGTGCC | 23062 |
rs778720821 | snp | A/G | 6.59609e-05 | 0.00574248 | | | GRCh38.p7 | 16:23494334 | GCTTCCTTCTCTTGC[A/G]GAGACTGGATCTTGT | 23062 |
rs778809190 | snp | G/T | 1.64732e-05 | 0.0028699 | missense | GGA2 | GRCh38.p7 | 16:23486763 | GAAGGTCCTCGGGGT[G/T]GTTGCTCTTTAGAAG | 23062 |
rs778825133 | in-del | -/GT | | | intron-variant | GGA2 | GRCh38.p7 | 16:23509776 | CACACACACACACAC[-/GT]GTGTGTGTGTTTAAA | 23062 |
rs778895170 | snp | A/G | 3.64146e-05 | 0.00426685 | intron-variant | GGA2 | GRCh38.p7 | 16:23479023 | AGTCTAGACAAATAA[A/G]CAACTTACTGAAGGT | 23062 |
rs778934315 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23505544 | ATGACAGAATGCACA[C/G]GCGCTGCCGTTTGTA | 23062 |
rs778984779 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23473156 | TAAAAATGGTATAGG[C/T]TTATAAAGTAACAGT | 23062 |
rs779006805 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | GGA2 | GRCh38.p7 | 16:23488652 | GAGCTCTTGGGCCAG[A/G]GAGATGGTGGGGGTA | 23062 |
rs779059654 | snp | C/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23502336 | CTTACCCCAGGCCGA[C/T]AATGGTCATGCCACC | 23062 |
rs779060797 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23504878 | TTCAAGCGTGCTACA[G/T]GGCCAGAGGTGTTAA | 23062 |
rs779086522 | in-del | -/G | 1.76858e-05 | 0.00297365 | intron-variant | GGA2 | GRCh38.p7 | 16:23467703 | AGCGGATAGGTTCCT[-/G]GGACAGAAGAGACAG | 23062 |
rs779108861 | in-del | -/AC | | | intron-variant | GGA2 | GRCh38.p7 | 16:23475155 | CAAGGAAAAAATAAC[-/AC]ACACACACACACACA | 23062 |
rs779169108 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23482440 | CCTCTCTCATGTTTC[A/G]AGATTTTCCACAATA | 23062 |
rs779194591 | snp | A/C | 1.68216e-05 | 0.00290009 | intron-variant | GGA2 | GRCh38.p7 | 16:23485979 | CAAACCCACTTTAGT[A/C]AACATGTGCAGCCCC | 23062 |
rs779238463 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23508832 | CAAACTCCACATCTC[A/C]ACCTTCTCTGCCTAA | 23062 |
rs779281579 | snp | A/G | 0.00162513 | 0.0284592 | utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23510438 | CGACGCTGCGGCCGC[A/G]GGCGCCACTGCCTCT | 23062 |
rs779316362 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23469803 | GCATTGTTTAAGAAC[C/G]TATTTGGATTCACTC | 23062 |
rs779362062 | snp | C/T | 1.71085e-05 | 0.00292471 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23467671 | TCCACCTTGGTTGAA[C/T]GTCAGCTTGTACCGT | 23062 |
rs779385670 | snp | A/C/T | 6.6873e-05 | 0.00578211 | intron-variant | GGA2 | GRCh38.p7 | 16:23493513 | AGTGGTCCCAGGCTC[A/C/T]CCTCCAGGCTGGTAA | 23062 |
rs779390978 | snp | C/T | 1.66996e-05 | 0.00288956 | missense | GGA2 | GRCh38.p7 | 16:23482995 | GCTTTTCACACCTCT[C/T]ATACACGACCTGAAA | 23062 |
rs779457985 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23490657 | CAAGAATTACTTGAA[C/T]CCAGGAGGCGGAGGT | 23062 |
rs779476704 | snp | A/T | 6.53645e-05 | 0.00571646 | intron-variant | GGA2 | GRCh38.p7 | 16:23495829 | TAGGAAGAAATTTAC[A/T]CCCCTCCCCATACAC | 23062 |
rs779536673 | in-del | -/GA | 0.0001261 | 0.0079394 | intron-variant | GGA2 | GRCh38.p7 | 16:23478329 | AGGAACCGCACTCAG[-/GA]GCCACACTCTCCCAC | 23062 |
rs779580450 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23485994 | AAACATGTGCAGCCC[C/T]CTGTGTTACACCTGT | 23062 |
rs779728980 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23477518 | GGAGGCTGAGGCAGA[C/T]GGATCATGAGGTCAA | 23062 |
rs779736896 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23490472 | GGGAGCGGTGGCTCA[C/T]GCCTGTAATTCCAGC | 23062 |
rs779762062 | snp | C/T | 4.94874e-05 | 0.00497406 | missense | GGA2 | GRCh38.p7 | 16:23493431 | TGTGGAACTTCTCCC[C/T]ACAGTGGTTCATGCA | 23062 |
rs779834299 | snp | C/T | 1.72689e-05 | 0.00293839 | missense | GGA2 | GRCh38.p7 | 16:23467643 | TCACTTCTCCTACTT[C/T]GCTGAAAGGCTGTCC | 23062 |
rs779888466 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23478547 | CAGGGTATGAATGAC[C/T]ATCAGCCACAGTAAA | 23062 |
rs779906456 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23464060 | GGATTAATATTGTAG[C/T]AGGCAAGCACTATTT | 23062 |
rs780012291 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23484907 | TCACATAAAAACTTG[C/G]ACAAAGTTCAAAGTC | 23062 |
rs780012475 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23469366 | CTTATAAAACAGAGG[C/T]AGTAGCAGAACATTG | 23062 |
rs780139478 | snp | C/G | 1.65647e-05 | 0.00287786 | intron-variant | GGA2 | GRCh38.p7 | 16:23480615 | GGCTGCCCCAAGGCA[C/G]AGAAGGCAAGGAGAA | 23062 |
rs780173906 | snp | C/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500735 | CGGAGGTGGCAGTAG[C/T]GCCACACCCCACTGC | 23062 |
rs780214963 | snp | C/T | 1.77146e-05 | 0.00297607 | missense | GGA2 | GRCh38.p7 | 16:23478374 | AAGACTCACAGAGGG[C/T]ACGGAGCTGGCTGTG | 23062 |
rs780259729 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23482378 | AAATCAGCTATGAGC[C/T]GGTAATTATTAAAGA | 23062 |
rs780306056 | snp | C/T | 1.68545e-05 | 0.00290292 | intron-variant | GGA2 | GRCh38.p7 | 16:23469018 | GGGGAAGAAAACCAA[C/T]ATGTAACTCATTCCT | 23062 |
rs780327627 | snp | A/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23483840 | TTAGTAGAGATGGGG[A/T]TTCTCCATGTTGGTC | 23062 |
rs780331866 | snp | G/T | 1.69424e-05 | 0.00291048 | intron-variant | GGA2 | GRCh38.p7 | 16:23478850 | CTGAGACCCTCCCAT[G/T]CTCTCTCCGGGCCCT | 23062 |
rs780355430 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23489257 | TTGTTGTTTTTGAGA[C/G]AGATTCTTGCTCTGT | 23062 |
rs780398494 | snp | G/T | 1.66261e-05 | 0.00288319 | intron-variant | GGA2 | GRCh38.p7 | 16:23468864 | CCCCCATCTCCCTGC[G/T]ACCACAGACACTGGA | 23062 |
rs780478100 | snp | C/T | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504290 | ACTCTTGCGGTGAGG[C/T]CTTCAGTTCCTTGAC | 23062 |
rs780483715 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23494465 | AGTAAAATCACTTTT[A/C]TTCCAGGGGCTGGTG | 23062 |
rs780483847 | snp | G/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23502060 | AGTGGTCTGAGCTGA[G/T]CTGGAGTCCAAAAAA | 23062 |
rs780494771 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23469654 | ATGTGCTTCATGCCC[A/G]GTGAGAGTTTCTGAG | 23062 |
rs780497946 | in-del | -/TCG | 1.65455e-05 | 0.00287619 | cds-indel | GGA2 | GRCh38.p7 | 16:23482934 | TTACCGAGTGCATCA[-/TCG]TCATCAGTGGTGTCA | 23062 |
rs780516710 | snp | C/T | 1.64749e-05 | 0.00287005 | missense | GGA2 | GRCh38.p7 | 16:23486097 | ACCTTCACATGGCTT[C/T]GCACTTCCTCCACCG | 23062 |
rs780527875 | snp | A/G | 4.75229e-05 | 0.00487434 | intron-variant | GGA2 | GRCh38.p7 | 16:23478766 | TGGACCTCCAAGGCC[A/G]TGATCCCACCGGGAC | 23062 |
rs780555702 | in-del | -/G | 1.68194e-05 | 0.0028999 | intron-variant | GGA2 | GRCh38.p7 | 16:23478859 | TCCCATTCTCTCTCC[-/G]GGCCCTGGGAAGGGC | 23062 |
rs780575088 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23510039 | AAAGCGCAGGTCACG[G/T]AGCCATTGGGGTGGG | 23062 |
rs780587863 | in-del | -/CC | 1.73054e-05 | 0.00294149 | intron-variant | GGA2 | GRCh38.p7 | 16:23478708 | TGGTGCAACCTGTCT[-/CC]CCCCCAGGTATCAGC | 23062 |
rs780604866 | snp | A/G | 1.67089e-05 | 0.00289035 | intron-variant | GGA2 | GRCh38.p7 | 16:23478870 | CTCCGGGCCCTGGGA[A/G]GGGCATCCTTACCAT | 23062 |
rs780614513 | snp | C/G | 4.94482e-05 | 0.00497209 | intron-variant | GGA2 | GRCh38.p7 | 16:23491645 | TACAGGCCTAGTCAA[C/G]AGGAAATAAGACACA | 23062 |
rs780664680 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23488220 | CCCACACTCCCCACG[A/G]GCTATCCTTCTGCAC | 23062 |
rs780683292 | snp | A/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501243 | TGGTGTACATCGAAC[A/G]ACTTTTAACTAATGG | 23062 |
rs780703270 | snp | A/G | 0.00039862 | 0.0141121 | intron-variant | GGA2 | GRCh38.p7 | 16:23478785 | TCCCACCGGGACAGT[A/G]CAGGAGCACCTCTCT | 23062 |
rs780777265 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23507178 | GCCTTCCCCAAATTA[G/T]GGGCCAAAGTAGGCA | 23062 |
rs780790854 | snp | G/T | 3.29598e-05 | 0.00405941 | missense | GGA2 | GRCh38.p7 | 16:23474936 | AAAGGGACAAACACT[G/T]GAGCCAGAGGTGTAT | 23062 |
rs780895383 | snp | C/T | 1.65699e-05 | 0.00287831 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23486015 | TTACACCTGTATTAC[C/T]TGCAGGGCCTCCTGG | 23062 |
rs780930713 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23508255 | TATTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 23062 |
rs780938327 | in-del | -/A | 1.64743e-05 | 0.00287 | frameshift-variant | GGA2 | GRCh38.p7 | 16:23486082 | AGCATCTCCTGCAGC[-/A]CCTTCACATGGCTTC | 23062 |
rs780984586 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23477452 | TGCTGCCACATAAGA[C/T]ACGCCTTTTGGCTGA | 23062 |
rs780990113 | snp | C/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500243 | CCAGCGTGCCTTTGC[C/T]GGGAAGAGGTATAAG | 23062 |
rs781039681 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23476275 | CCTCTGGGTGGCAAA[C/T]GGGAATGAACTCCCA | 23062 |
rs781116311 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23483475 | AAATAAAGAAGTTAC[A/G]TGGAGGCTGGCTCTC | 23062 |
rs781142094 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23474136 | CTGCCTTAAGGAGGA[G/T]CCCTAGAGAAGGAGG | 23062 |
rs781185289 | snp | C/T | 2.36605e-05 | 0.00343943 | intron-variant | GGA2 | GRCh38.p7 | 16:23493516 | GGTCCCAGGCTCCCC[C/T]CCAGGCTGGTAATCA | 23062 |
rs781211448 | snp | C/T | 1.65002e-05 | 0.00287225 | missense, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23494349 | GGAGACTGGATCTTG[C/T]GGGCCAGTAGCCAGG | 23062 |
rs781245596 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23496457 | ACAGAAGAGAGGCCA[C/T]CTGGAAGTGTCTCAG | 23062 |
rs781300302 | snp | C/T | 1.75265e-05 | 0.00296023 | intron-variant | GGA2 | GRCh38.p7 | 16:23495657 | CTCAGTGTGGGGTGC[C/T]CCCAGAGTCAACTAT | 23062 |
rs781321063 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23480550 | GTTCTCTCATTTCTA[C/T]TCCTTAACCCAGAAT | 23062 |
rs781327052 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23492632 | CCTTGCCTATGTATC[A/G]CTTCCATTTGTATCC | 23062 |
rs781364790 | snp | C/T | 3.2244e-05 | 0.00401509 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467548 | AGACAGCAAAAGTAA[C/T]GCCAGCCTAAGCTTG | 23062 |
rs781385163 | snp | C/T | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504597 | AGCAGCTCCAAAAAA[C/T]GACCCCCAGGGGGCC | 23062 |
rs781385674 | snp | A/G | 9.88338e-05 | 0.00702902 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23486722 | CACCTCCTTGACCAA[A/G]TTCTTGATTAACCGG | 23062 |
rs781408119 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23493186 | ACAGTGAGGGGCAGG[A/G]GTCAGCTAATGAGCA | 23062 |
rs781409146 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23509804 | TAAAAAAAAAAGTCT[C/G]GCCAAAGTAAACACA | 23062 |
rs781455957 | snp | A/G | 3.31049e-05 | 0.00406834 | intron-variant | GGA2 | GRCh38.p7 | 16:23493316 | GGAGTTTGACAGTGG[A/G]CGTAGGTGCGACACA | 23062 |
rs781529863 | in-del | -/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23470828 | ATGAAATAAATGCTT[-/T]TTTTTTTTTTTTTTT | 23062 |
rs781552536 | snp | C/T | 1.73613e-05 | 0.00294624 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23478388 | GCACGGAGCTGGCTG[C/T]GCTGAGAGGAGGTCC | 23062 |
rs781558727 | snp | C/T | 1.65427e-05 | 0.00287595 | missense | GGA2 | GRCh38.p7 | 16:23482935 | TACCGAGTGCATCAT[C/T]GTCATCAGTGGTGTC | 23062 |
rs781573550 | snp | A/T | 1.64727e-05 | 0.00286986 | missense | GGA2 | GRCh38.p7 | 16:23491745 | CAGACTGTCCAACTG[A/T]AGAGTATTTCAATGA | 23062 |
rs781632338 | snp | A/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23507952 | GTGACACAGTGAGAC[A/T]CTGTTTCAAAAAAAG | 23062 |
rs781635161 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23481312 | CAGGAGACGGAGGTT[G/T]CAGCGAGCTGAGATC | 23062 |
rs781654354 | snp | A/G | 1.72991e-05 | 0.00294096 | intron-variant | GGA2 | GRCh38.p7 | 16:23469047 | CTAACCACAGCTTCT[A/G]GGATGGAGATCAGGT | 23062 |
rs781714939 | snp | A/C | 1.98045e-05 | 0.00314672 | intron-variant | GGA2 | GRCh38.p7 | 16:23478968 | ACCTGCTTCCAGATG[A/C]AGAGTAATGCCACAC | 23062 |
rs781719994 | snp | C/G | 1.6513e-05 | 0.00287336 | intron-variant | GGA2 | GRCh38.p7 | 16:23480783 | CCGCTGAAGAATGAG[C/G]GAAGACTCAGAACCC | 23062 |
rs781782058 | snp | A/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499927 | GCTCCCGCATCACGA[A/T]GGGAACAGGGCATGT | 23062 |
rs796126452 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23475336 | CTGGGATTACAGGCA[C/G]CTGCCACCATGTCCG | 23062 |
rs796160846 | in-del | -/A | | | intron-variant | GGA2 | GRCh38.p7 | 16:23497122 | aaacaaaaaaaaaaa[-/A]caaCCACCCTTCCAA | 23062 |
rs796435743 | in-del | -/A | | | intron-variant | GGA2 | GRCh38.p7 | 16:23481216 | AACCCAGTTTCTACT[-/A]AAAAATACAAAAAAT | 23062 |
rs796501597 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23478215 | AAAAAAAAAAAAAAA[A/G]AAAAAAAGACAAAAA | 23062 |
rs796508716 | in-del | -/TA | | | intron-variant | GGA2 | GRCh38.p7 | 16:23471381 | TTGAGGGGGGAAAAC[-/TA]TGTAAGACTGACCAA | 23062 |
rs796536815 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23509273 | CGGATTCCTGAGCTT[C/T]AGGCTTGCACTCCAG | 23062 |
rs796636732 | in-del | -/AA | | | intron-variant | GGA2 | GRCh38.p7 | 16:23474867 | AATAGATTCCCAGGG[-/AA]AAAAAAAAAAAGGTG | 23062 |
rs796754521 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23497811 | CATGTACTTGGACTC[A/G]CTGAGCCTCAGTTTC | 23062 |
rs796807798 | in-del | -/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23470209 | TAACACCACTACAAA[-/C]CCCCCGGACAGCCAG | 23062 |
rs796844875 | snp | A/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467271 | ACCTGAGGCAGGGAC[A/G]GTGTCGCTCGCTGAC | 23062 |