SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs540695210 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202902073 | ATTACCCATAGTTCC[A/G]CAATACAAAGACACA | 59349 |
rs540702981 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202920502 | CTGGCTCAGCCTCCC[A/G]AGTAGTTTGGACTAC | 59349 |
rs540940131 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202914633 | AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 59349 |
rs541046152 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909691 | TGGCCTATATGAACT[G/T]TGTCAATAGGGCTTC | 59349 |
rs541191609 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896379 | ACTTTTTTGTAGAGA[A/C]AGAGTCTCACCATAT | 59349 |
rs541232203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202904081 | TGGAGTGCAATGGCA[C/T]GATCTTGGTTCACCA | 59349 |
rs541234397 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926500 | GTGATTCATCAAAGC[A/G]TATGTTTTTCAAAAA | 59349 |
rs541375027 | in-del | -/CTTG | 0.00318978 | 0.0398085 | intron-variant | KLHL12 | GRCh38.p7 | 1:202926194 | ATCGATGGACTTACA[-/CTTG]CTTAAGATATTGAAG | 59349 |
rs541418190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202917278 | AGAGTGCAGTGGTGC[A/G]ATCATGGCTCACTGC | 59349 |
rs541454944 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923957 | CATACATGTAAGTGT[A/C]AATTATATAATAAAC | 59349 |
rs541455236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202916383 | TTAAGGCCAGGAGCC[A/G]TGGCTCACACTTATA | 59349 |
rs541588353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202892796 | GACCAGCCTGGGCAA[C/T]ATGGTGAGACCCTGT | 59349 |
rs541690152 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927914 | TAGAACCTGGGAGGC[A/G]GAGGTTGCTGAGCCG | 59349 |
rs541784303 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906663 | ATATATTTTATTTAA[A/T]TAATTTATTTATTTT | 59349 |
rs541862985 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905865 | GCTGGAGTGCAGTGG[C/G]GTGATCTCAGCTTAC | 59349 |
rs541972072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900622 | TAATCACAGCACTTT[A/G]GGAGGCCGAGGCGGG | 59349 |
rs542030316 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202902419 | TGGGTAACAGAGCGA[A/G]ACTCCGTCCAAAAAA | 59349 |
rs542051701 | in-del | -/TATG | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202903996 | ATCTATCTATGTATC[-/TATG]TATCTATCTATCTAT | 59349 |
rs542070288 | in-del | -/A | | | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929509 | CTCTATTATTGGTGT[-/A]AAAAGGTGGAAGATA | 59349 |
rs542186358 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202897266 | TGGAGACAGAGTTTC[A/G]CTCTTGTTGACCAGG | 59349 |
rs542187499 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907083 | TCCTTCAATCTATCT[G/T]GTGTTGATATGTATC | 59349 |
rs542207416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897926 | CAACTATATGATCAC[A/G]TTCCCTGCCAATTCA | 59349 |
rs542351483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905278 | TACCTCCAAAGAATC[G/T]TCTGGGTTTACTGAT | 59349 |
rs542352882 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909398 | TCTATCGCAGCGCTT[A/C]CATTTAACTATTTTT | 59349 |
rs542396777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901609 | ACCAGCCACTCAGGG[A/G]TTTTATGGCTCTAAA | 59349 |
rs542486417 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904764 | GTTAGAGAAATAAGG[C/T]AGATGCAGGACTGCT | 59349 |
rs542578200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895402 | CTGTCTCAAATAATA[A/G]TAACATTTGACCTTA | 59349 |
rs542581731 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896204 | TACAAACTTTTTTTT[C/T]CTGAGTTGGGATCTC | 59349 |
rs542617244 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202905768 | AAGTTTTAGATCTTG[A/G]AGCATTTTGAATTTC | 59349 |
rs542644663 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921942 | GTCACTAGCACATTA[C/T]TTTGAAAAAACATAT | 59349 |
rs542770974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914268 | GCCAAGAGCTAGAAG[A/G]GGTTAGATGCTGCTC | 59349 |
rs542788645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908907 | AAGAAAAGGTCTGAA[A/G]CGAGGTGTCTGTACT | 59349 |
rs542790596 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202915990 | TTATATGTAGTGAAC[A/G]TCAAATCTGTAGTGC | 59349 |
rs542795457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924063 | TGGGATCTTGAAAAA[C/T]AAAGATTTGCAATGT | 59349 |
rs542827774 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202915264 | CAAGACTAAATCCCA[C/G]TTGGACTCTAAAACC | 59349 |
rs542864239 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914564 | AGGTTTTTTAGTTTG[C/T]GTTTTTAAGACTAAT | 59349 |
rs543018315 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929825 | AGAGCACGCCTCAAA[A/C]TATATTTATATGTTC | 59349 |
rs543132622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893495 | TATAGAAATAAACTA[C/T]GGTCACTAATGACTA | 59349 |
rs543185396 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905949 | AGCTTGAACTACAGG[G/T]GCCCGCCACCACACC | 59349 |
rs543187282 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920219 | CTCAGGAGGCTGAGG[C/G]AGGAGAATTGCTTCA | 59349 |
rs543223976 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912393 | GCTTCATCCAGCCAA[A/C]GAAGTCGAAGTGGTT | 59349 |
rs543400927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919551 | GCTCTCTTTTATAGA[A/G]CCAAATACTCATATC | 59349 |
rs543428980 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925922 | GCAGCCTGGCCAACA[A/T]GGTGAAACCTAGTCT | 59349 |
rs543465728 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202899685 | ACAAAAATTAGCCGG[A/G]TGCAGTGATGCGCAC | 59349 |
rs543466200 | snp | C/T | 1.6636e-05 | 0.00288405 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918164 | TAACATCAAGACAAA[C/T]CCGTACCTGAATTTC | 59349 |
rs543502795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924840 | AGTGGTAGATCTTAT[C/T]CAGAATCTGCCAAAA | 59349 |
rs543572478 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911996 | GCTTTGGGTTTGTCA[C/T]ATATGCCATTGTGGA | 59349 |
rs543985182 | in-del | -/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202921114 | TCCCAGGTTCAAGTG[-/T]TTTCTCGTGCCTCAG | 59349 |
rs543986883 | in-del | -/C | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900223 | TAACTCCCTGCCCCA[-/C]CCCCCAACCCCCCAA | 59349 |
rs543999383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897142 | TTTTCCTTGAGGCTG[C/T]AGCTCTCGAGTCTCT | 59349 |
rs544047500 | in-del | -/C | 0.00318978 | 0.0398085 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891987 | CTCTCTCTCCCTTGT[-/C]CCCAAAGTTTTGTGG | 59349 |
rs544107965 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202893485 | GAATCTGAATTATAG[A/T]AATAAACTACGGTCA | 59349 |
rs544121166 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202923502 | TGAGCATTGGCTCAT[A/C]GTATTTTTAACTATA | 59349 |
rs544135222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202926306 | CTTTCTGAAATGATC[C/T]GGGGGGAAGGAAATC | 59349 |
rs544175638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893554 | GGAATGGGCCCACAC[A/G]GGCCTAGAATAATCT | 59349 |
rs544203284 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899475 | TTATGTACTTGCCAA[A/T]TAAAGTGGACCCTCT | 59349 |
rs544205579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914295 | GCTCTGGTACATTAG[A/G]CAAAAGGTGACGGTG | 59349 |
rs544238342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907184 | GCCCTATCTAAAAGT[C/T]CTCTTTTTAAAAAAA | 59349 |
rs544246790 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891910 | ATTCAGTTTAATTCA[C/T]TTAATTCTAACTTCA | 59349 |
rs544426433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928215 | GGGAGGCGGAGGTTG[C/T]AGTGAGCTGAGATCG | 59349 |
rs544463297 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927356 | GTACCCTAGCGCGGG[G/T]CTTCTGTACGCTGCT | 59349 |
rs544515856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901364 | TCGACCTCCCAGGCT[C/T]AAGCAATCCTCCTAC | 59349 |
rs544550803 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900681 | CCAGCCTGGCCAACA[G/T]GGTGAAACCCCATCT | 59349 |
rs544566755 | snp | C/G | | | missense | KLHL12 | GRCh38.p7 | 1:202911099 | GGGGGTTAGTAGGGG[C/G]ATCCGCACATACTGT | 59349 |
rs544726140 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202898884 | AAATTACACAAACAC[A/G]TGAGAATAAGGAATT | 59349 |
rs544739430 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202903151 | GGAGCCAGAGTGAGA[A/C]CTTGTCTCAAAAAAA | 59349 |
rs544861657 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924372 | TTCACATATTGTTAG[A/G]AGGAGTGGGATGTGG | 59349 |
rs544918073 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892472 | CTGGAAAGGATTTTT[G/T]ATTCTCCCACTAACT | 59349 |
rs545057489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202915446 | TTCTTTCCAGAAAAA[A/G]AGCAAAGGGCAGTCT | 59349 |
rs545172436 | snp | C/T | 6.59348e-05 | 0.00574135 | missense | KLHL12 | GRCh38.p7 | 1:202918182 | GTACCTGAATTTCGT[C/T]GCACTTGATTAGCTT | 59349 |
rs545259753 | in-del | -/TTTTAATATTTTTAA | 0.00199481 | 0.0315187 | utr-variant-3-prime, upstream-variant-2KB | KLHL12, RABIF | GRCh38.p7 | 1:202891131 | GCATTTGAGACCGTT[-/TTTTAATATTTTTAA]GATTTTTAATATTTT | 59349 |
rs545329656 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202914070 | AGTGAATGAGGGTGA[C/T]AGAGGAGTAAAATAT | 59349 |
rs545451365 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202897577 | CATAATCCTTGAGGT[C/T]TTAAGTGCAGGTGAG | 59349 |
rs545560228 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929918 | GAGAGGCCGAGGCGG[G/T]CGGATCACCTGAGGT | 59349 |
rs545566263 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899584 | TAATCCTAGCACTTT[C/G]GGAGGCCAAAGCAGG | 59349 |
rs545595520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909529 | GTGACAGGAAGAATC[A/G]TATTTTGTCTGAAAT | 59349 |
rs545796021 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202916257 | GCTGGAAAATAATTC[C/T]TCTACAGTTGGAACC | 59349 |
rs545833991 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919684 | ATGTTCATGATTAAG[C/T]TTACACTATTAATTT | 59349 |
rs545870756 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202926828 | CTAAATTCTAGAGAA[A/G]GAAACGAAGTCCTTC | 59349 |
rs545950367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907011 | CTTCCATCCAGAAGG[C/T]ATACAAATATTTTCC | 59349 |
rs545957383 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202907093 | TATCTTGTGTTGATA[C/T]GTATCTGTGTATAAA | 59349 |
rs546037935 | snp | A/C | 0.0023933 | 0.0345097 | downstream-variant-500B, upstream-variant-2KB | KLHL12, RABIF | GRCh38.p7 | 1:202890967 | AGTGTAAAGTGGCTA[A/C]CTCTTACCTGTGTCT | 59349 |
rs546091449 | snp | C/T | | | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929836 | CAAAATATATTTATA[C/T]GTTCAATTTTTTAAA | 59349 |
rs546188537 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905157 | ACCTCAAGACTATGA[A/T]GATATATAGATTTAT | 59349 |
rs546271999 | in-del | -/AACT | 0.00835141 | 0.0640778 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923853 | ACACTAAGATGATAG[-/AACT]AACTAAAAAAAAAAC | 59349 |
rs546322357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911569 | CTTCTGGTCTTCTCT[A/G]TAACTTTAAGGAAGG | 59349 |
rs546377255 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202924535 | GAGGCCAAGGCAGGA[A/G]GATTGCTTGAGCCCA | 59349 |
rs546503694 | snp | C/G | | | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927353 | TCTGTACCCTAGCGC[C/G]GGGCTTCTGTACGCT | 59349 |
rs546556512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897825 | TTCTCCTGCCTCAGC[C/T]TCCCAAAGTGCTGGG | 59349 |
rs546619950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893019 | GTCTGGCACAGTGGC[A/G]TGCACCTGTGGTCCC | 59349 |
rs546655967 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | KLHL12 | GRCh38.p7 | 1:202927159 | GAGTGCGGCGCGGGG[A/C/T]TAGCAGGCGGCTCGG | 59349 |
rs546809295 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922516 | TTTTGAGACAGAGTC[C/T]CGCTCTGTCACCCAG | 59349 |
rs546845877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922074 | CATGTATTCCAGAAA[C/T]TTCTCATTCAATAAA | 59349 |
rs546894369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906765 | CTCCCGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 59349 |
rs546978431 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202917878 | TGTGAAATGAGTGAA[C/T]GGGTAATAGAGAAGT | 59349 |
rs547090313 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202899797 | CACTGCACTCCAGAC[C/T]AGGCAACAGAGTAAG | 59349 |
rs547432940 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923457 | TGGAATGACCTGTCA[C/G]GTTCCTGTTTTCCCT | 59349 |
rs547529621 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908350 | TATTTGCTAAGATAA[A/T]AGCTAATACACATAG | 59349 |
rs547582342 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202903758 | CTCCCCAATAGCTGG[C/G]ATTACAGGCATGCGT | 59349 |
rs547587877 | snp | C/T | 1.68966e-05 | 0.00290655 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202895714 | GTCTCTTACGAGTGA[C/T]GCTCTATGGATTTGG | 59349 |
rs547722160 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895101 | TGAAAGCAAAAAGGA[G/T]TATTTGTCGGCTGGG | 59349 |
rs547749265 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901963 | TCCCTGTTGAAAAGA[A/C]TTGAAAAGTATTTTC | 59349 |
rs547857347 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899138 | GCCAACAAGGCAAAA[A/C]CCCGTCTCTACTAAA | 59349 |
rs547864700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202915528 | ATTTAAGCTTCTAAA[C/T]AAGGTTAGTTATTTG | 59349 |
rs547891912 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905962 | GGTGCCCGCCACCAC[A/C]CCTGGCTTTTTTTTT | 59349 |
rs547996937 | in-del | -/A | 0.477175 | 0.104362 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914865 | AGCGAAACTCCGTCT[-/A]AAAAAAAAAAAAAAA | 59349 |
rs548201594 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202919487 | TATGTAAGAAAACAC[A/G]TAATTTCTCCTTCCT | 59349 |
rs548564972 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202926092 | CCTGGGCAACAGAGC[A/G]AGACTCTGTCTCAAA | 59349 |
rs548659688 | in-del | -/ACC | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202926852 | GTCCTTCCTCCTAAT[-/ACC]ACCAGGCATATGGCC | 59349 |
rs548790925 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912165 | TAAAGAAGACACTGA[A/T]GAACATCACCTAAGA | 59349 |
rs548825762 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919283 | AAAAACCTGGGAATT[A/G/T]TAAGGGAAAACAAAC | 59349 |
rs548897081 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202896663 | AGGGCCACTGACATT[G/T]CTAAGGCATAATCTT | 59349 |
rs548954653 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914090 | GAGTAAAATATGAAG[A/C]TGGAGAGTTAAGCAA | 59349 |
rs548989151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913698 | CAAGGAAGGCCTCCC[A/G]GAAGAAGCAACAAAT | 59349 |
rs549102745 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893926 | GATATTTATTAAGCA[G/T]GTACTACACAGGCAA | 59349 |
rs549171437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920703 | TTTTAATAAAGCAAA[C/T]ATGGCACATTATCTG | 59349 |
rs549181264 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908071 | TATAGAGTAATTCAT[A/G]ACTTATAAAATGTTT | 59349 |
rs549218255 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907425 | TGGTCAACATGGAGA[A/G]ACCCTGTCTCTACCA | 59349 |
rs549223713 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202915653 | AACTGAAAACATGAC[A/G]AGCTCATAGTTGAGT | 59349 |
rs549290359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893158 | TACCCAAGTCTTGTC[C/T]CTGTCCAAAAATGAG | 59349 |
rs549384766 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921175 | ACCACTACAACCAGC[C/T]AATTTTTTTTTTTTT | 59349 |
rs549391170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911266 | TCACCATCTCAAAAC[A/G]TAACCACGTTCACTT | 59349 |
rs549533061 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918438 | AGTTGGACAGGTGTG[A/T]TCTAGGATATATTCT | 59349 |
rs549575549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905412 | CTGAACATTAACTCT[A/G]TTGATATAAAGAACT | 59349 |
rs549680298 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202898132 | TGGTCTCAAACTCCC[A/G]GCCTCAAGCGATACT | 59349 |
rs549712381 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202904582 | TCTGCCAATGATGGA[C/G]TACTTGTTAAGTGAG | 59349 |
rs549807870 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202917961 | GAATAGTGATTCTTA[A/C]CCACTGGGATCATAT | 59349 |
rs549956946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897331 | ACCTCTGCCTCCTGG[A/G]CTCAAGTGATTCTCC | 59349 |
rs549958064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202917588 | AGTTATGATTTGGCT[C/T]CTGCTTCTGTAGATC | 59349 |
rs550206287 | snp | C/G | | | downstream-variant-500B, upstream-variant-2KB | KLHL12, RABIF | GRCh38.p7 | 1:202890651 | ATGCACAATCCATCT[C/G]CCAAAGTTGGTAGGC | 59349 |
rs550208116 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202902732 | TGGTGGCTCACACCT[C/G]TAACCCTAGCACTTT | 59349 |
rs550247475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896510 | CTTCTGAGCTCAACT[A/G]AACACTGGGTTCAAT | 59349 |
rs550347294 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924455 | TTAAAAATTTTTAAA[A/C]TTTAGAAGGAAAAAA | 59349 |
rs550498253 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921216 | GTCTTGCTCTGTTGC[C/T]CAGGCTGGAGTGCAG | 59349 |
rs550557194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | KLHL12 | GRCh38.p7 | 1:202927144 | CAGCCTGTGGGGATG[A/G]AGTGCGGCGCGGGGC | 59349 |
rs550602828 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899760 | GAACTGAGGAAGAGG[G/T]TGCAGTGAGCCGAGA | 59349 |
rs550745807 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906754 | GCAACCTCCGCCTCC[C/T]GGGTTCAAGCGATTC | 59349 |
rs550883171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202892836 | ATTTAAAGAAAGAAA[A/G]AAAGAAATTAGCCTT | 59349 |
rs551092523 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202930231 | TACTTTAATGATATT[A/G]CCTAATTCCTGACTG | 59349 |
rs551168110 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202902731 | ATGGTGGCTCACACC[A/T]GTAACCCTAGCACTT | 59349 |
rs551269636 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202910917 | CTTGGGGACTACCCA[C/G]CACCACTCTCACTGG | 59349 |
rs551568606 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908948 | TATTATTTTCAACTA[C/T]GTTGTCACCTGCAAG | 59349 |
rs551574535 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909938 | TTCTTTATTAAAAAA[A/T]ACTCTTCTAAAATTG | 59349 |
rs551608686 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202916584 | AGAAGGTGAAGGTTA[C/G]AGTGAGCTGAGATCA | 59349 |
rs551651531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912496 | TGGCAGTGAGGATGG[C/T]GATAATGGATTTGGT | 59349 |
rs551663229 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202915377 | ACTGGGAGTCAGACA[C/T]CTGGTTCCTATTTCT | 59349 |
rs551694751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894075 | GAGACAAGGAGGAGA[A/G]CAGAATCTCATTTTT | 59349 |
rs551702055 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901065 | AAAATAAAGAAAAAA[A/C]CCCTCTCTTTCTTGA | 59349 |
rs551774449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914634 | GCACTTTGGGAGGCC[A/G]AGGCGGGTGGATCAC | 59349 |
rs551875969 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | KLHL12 | GRCh38.p7 | 1:202917916 | AGATACCTACTTTAC[-/T]TCCAATTTCTGCTTA | 59349 |
rs551905759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912095 | CTGTTTCAAGGGAAG[A/G]TTCTCAAAGACCAGG | 59349 |
rs551920505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894926 | AAAAAGAATGGGGTA[A/G]AACAAAATCCTTAAA | 59349 |
rs551925047 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891267 | CACTCCTAATACCCA[C/T]AAAACAAGAATTTCA | 59349 |
rs551963778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202898972 | TCTTTTAGAGACACA[C/T]GTGGAAGTATGACAC | 59349 |
rs551963884 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | KLHL12, RABIF | GRCh38.p7 | 1:202890696 | ATAACTTCCTCATGT[A/G]GCTCCTCCTTCCTTT | 59349 |
rs552249255 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202902671 | AGAAATGGGAAGAAT[A/G]CTGAGTAATGAACCT | 59349 |
rs552393654 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922402 | GAAACCCCGTCTCCA[C/T]TAAAAATACAAAAAA | 59349 |
rs552424872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921125 | AAGTGTTTCTCGTGC[C/T]TCAGCCTCCCAAGTA | 59349 |
rs552563608 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202917929 | ACTTCCAATTTCTGC[C/T]TATTCTATACTCTGT | 59349 |
rs552745782 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202922766 | GCTGGGATTACAGGC[A/G]TGAGCCACCACGCCC | 59349 |
rs552770055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927273 | ATGACGCAATGCAGC[C/T]GGAGCACCGCCCTCC | 59349 |
rs552777463 | snp | A/G | | | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202896876 | AAGCTCCACTCCTGA[A/G]TCTTGGGGTCATATT | 59349 |
rs552834244 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925340 | GTTGAGGGCACTCCT[A/T]TGCCTGGCATCACCA | 59349 |
rs552917222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907061 | CTCATAGTTTTTCAC[C/T]ATTCAGTCCTTCAAT | 59349 |
rs553055521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918886 | TCACACTGTTTAAAT[C/T]ATGTATTAAAAACTA | 59349 |
rs553086687 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905823 | AACCCGATTTTTTTT[A/T]AGACAGAGTCTCACT | 59349 |
rs553120717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907814 | TTGGGAGGCTGAGGT[A/G]GGAAGACTGCTTGAG | 59349 |
rs553121931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912292 | ACCATGACTCTGTGA[A/G]TAAGACTGCCATTCA | 59349 |
rs553144568 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892418 | ATCACTGCACTGGTG[C/G]CTGTAATCACCCGGT | 59349 |
rs553230504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914167 | CAACTTGAAATCATC[C/T]GAAGGTTTCAAGCAG | 59349 |
rs553267400 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913826 | CCAATACACTACCCA[C/T]GCGTGGCTATTTACA | 59349 |
rs553269230 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921367 | TTTAGTAGAGATGGG[G/T]TTTCACCATGTTGGC | 59349 |
rs553381270 | snp | C/T | | | intron-variant, utr-variant-5-prime | KLHL12 | GRCh38.p7 | 1:202927163 | GCGGCGCGGGGCTAG[C/T]AGGCGGCTCGGGAGG | 59349 |
rs553452152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202915155 | GGCGTTCTTATTTTA[C/T]GCTCAGAACAGTCCT | 59349 |
rs553476035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202910093 | AAATAGTAGTAAACA[C/T]TTATGTACAAAGACT | 59349 |
rs553579615 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891734 | TACTGAACTCCCACA[C/T]TGATGTCATCTTCTC | 59349 |
rs553618309 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899416 | TTAATAAAACATATA[A/C]ACTCACACATAAACC | 59349 |
rs553654149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202898688 | GAAATTCTACAGGTC[A/G]AACAGCTTGGCTTCT | 59349 |
rs553717247 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202902340 | GAGGCTGAGGCAGGA[A/G]AATCGCTTGAACTTG | 59349 |
rs553724866 | snp | A/C | 0.000399281 | 0.0141238 | missense | KLHL12 | GRCh38.p7 | 1:202894268 | AATTTAAGATATTCA[A/C]GCCGTCATATCCTCC | 59349 |
rs553763426 | snp | A/G | 1.64833e-05 | 0.00287078 | synonymous-codon, intron-variant | KLHL12 | GRCh38.p7 | 1:202893313 | GGTCATACTGGTGAC[A/G]GTTGTCCAGGAATCA | 59349 |
rs553895398 | in-del | -/AGCCACTGTACC | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202901585 | GGGATTACAGACATG[-/AGCCACTGTACC]AGCCACTCAGGGGTT | 59349 |
rs553897387 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901145 | AGGAAATAGATTATA[C/T]TAAAAACACAGATAA | 59349 |
rs553984285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922291 | AGATAAAGGGGGGCC[A/G]GGCACATGGCTCAAG | 59349 |
rs554028126 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896101 | ATTTATTATAAGAAC[C/G]TTAAAAGGTAGGAGG | 59349 |
rs554064319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895288 | GTCCCAGCTACTCAG[A/G]AAGCTGAGGTGGGAG | 59349 |
rs554124828 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | KLHL12, RABIF | GRCh38.p7 | 1:202890837 | CCTGAAATTCAAGCG[C/T]GTGCTAAGTGAATTC | 59349 |
rs554339641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912332 | TCCTACGAATGGCCA[C/T]AACTGTGAAGTTAGG | 59349 |
rs554529231 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920040 | AATTACAGGCCAGGC[A/C/G]TGGTGGCTCATGCCT | 59349 |
rs554541275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202926597 | TGAAGACAGCCCGGG[A/G]GGTCTTTTATCGTTT | 59349 |
rs554566761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202898508 | TTGAGTGCTTCCTAA[C/T]GGTGATGAATAGGAA | 59349 |
rs554748547 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920184 | TTGGGCATGGTGGCA[C/G]ATGCCTGTAGTCCCA | 59349 |
rs554785502 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | KLHL12 | GRCh38.p7 | 1:202927203 | GCCGCCCAGACCCGG[A/C]GGCTCTGGAGGCTCT | 59349 |
rs554853621 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202904976 | TCCTTCTGCTGTATG[C/G]AGAAGAGTCATTATC | 59349 |
rs554964809 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926857 | TCCTCCTAATACCAC[C/T]AGGCATATGGCCGCC | 59349 |
rs554980678 | snp | C/T | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892110 | AAGACTTGGATTTTA[C/T]CAAGTTTACTTAAAC | 59349 |
rs555022922 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923982 | ATAAACAGTGATGCA[A/C]CCACAACTGAGCTTT | 59349 |
rs555143477 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920938 | AGAAATTTCATGTTC[C/G]TAGAGGAGCCTGTGG | 59349 |
rs555172853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202904165 | ATGTGCCACCAAGCC[C/T]GGCTAATTTTGTATT | 59349 |
rs555180355 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928119 | CTCCACTAAAAATAC[A/C]AAAAAATTGGCTGGG | 59349 |
rs555228770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911773 | GCCTGTGGACGCCGC[C/T]GAAGAAGCATCTTTA | 59349 |
rs555292403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900634 | TTTGGGAGGCCGAGG[C/T]GGGTGGATCACTTGA | 59349 |
rs555331769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906865 | TGGGGTTTCACCATG[C/T]TGGCCAGGCTGGTCT | 59349 |
rs555460017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899438 | ACATAAACCACGGAG[C/T]TTTTCTAAGAGGGCA | 59349 |
rs555523941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901225 | ACTATATGTCTACAG[C/T]GGAACTTCGTAAGAG | 59349 |
rs555622641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908524 | TTAATAAATCTAGTA[C/T]GAGGTAAACTGGTAC | 59349 |
rs555661469 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907907 | AGTGAGACCTCATTT[A/C]TATTAAAAAAAATAA | 59349 |
rs555764698 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL12 | GRCh38.p7 | 1:202903124 | AAGATCATGCCACTG[C/T]ACTCTAGCCTAGGAG | 59349 |
rs555792200 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202910297 | CAGAGTCTGTGCTCC[C/T]AAACACAATGTAAAG | 59349 |
rs555831696 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891873 | AATACTTCAGTGCTG[A/T]TCTAGGTTCACTCAC | 59349 |
rs556064563 | in-del | -/AGAG | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922865 | TTCAGGAAAAAAAAA[-/AGAG]AGAGAGAGAGAGACA | 59349 |
rs556130756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900997 | GTTGCAGTGAGCCGA[A/G]ATCATGCCGCTACAC | 59349 |
rs556229646 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant | KLHL12 | GRCh38.p7 | 1:202896890 | AGTCTTGGGGTCATA[C/T]TTCTCTACCACATCA | 59349 |
rs556271132 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202914085 | TAGAGGAGTAAAATA[C/T]GAAGCTGGAGAGTTA | 59349 |
rs556334182 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909446 | TTCCAGGGATTATGC[A/C]AACACAAGTACATAA | 59349 |
rs556478188 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202916875 | GCTACACAGGAGGAT[C/G]AGGTGGGAGAGCTGC | 59349 |
rs556514735 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923756 | TATGCACAACAATTA[C/G]TAGCACAGTACCTGG | 59349 |
rs556787308 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922788 | ACCACGCCCAGCTGA[A/C]GATCCAAGACTTAAC | 59349 |
rs556887587 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202930598 | AGTTATTTTAAAATG[C/T]ACAATTCAATTATTA | 59349 |
rs556910589 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913063 | CTGAATAAATGTCTT[A/T]AAAAAAAAACAAGAA | 59349 |
rs556975601 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927457 | GCAGGCCGAGGCGAG[C/T]GAATTACCTGAGCTC | 59349 |
rs557038614 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202926738 | CTATTTTCTAGAACT[G/T]TCGTTAACATCTGAA | 59349 |
rs557155137 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202918868 | TGCACTAATGCAAAA[A/G]CTTCACACTGTTTAA | 59349 |
rs557300053 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | KLHL12 | GRCh38.p7 | 1:202927225 | GGAGGCTCTGGAGCC[A/G]TCCGGGTCTGGCCCC | 59349 |
rs557386205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911831 | CTAAGTCAGAGTCTC[C/T]TAAAGAGCCCAAACA | 59349 |
rs557388684 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202909847 | AGGCTTAGGGGTTGT[C/T]AATAGCTTATGTCCT | 59349 |
rs557425008 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929615 | GAACTGTTTGGTTGT[A/G]AGACAGGGTGGGAAG | 59349 |
rs557436898 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921707 | GTTTAGCTAAGAGAA[C/G]AAATCTTCAATTTTA | 59349 |
rs557463978 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202915861 | AGTGGACAGGGATTT[G/T]TGTTTTGTTCATAAT | 59349 |
rs557501619 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL12 | GRCh38.p7 | 1:202898362 | TAACCTGGACTTGAA[A/G]GAGCAAATGTAGTAC | 59349 |
rs557576981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202898610 | CTAGTTTACAGGCAA[C/T]ACATGGGAGAAGAAC | 59349 |
rs557590643 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912196 | GATAATTTGAACAGT[A/C/T]TGGAAAAACGGAAGT | 59349 |
rs557590880 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906755 | CAACCTCCGCCTCCC[A/G]GGTTCAAGCGATTCT | 59349 |
rs557607639 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905684 | AACTATTTGCGCATC[C/T]CTAATTCAGAAACCC | 59349 |
rs557727117 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908598 | ACTGGGCTCCTTTTC[C/T]TCCTCTCTTCATTCC | 59349 |
rs557749409 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907499 | CCCAGCTACTCGGGA[A/G]TCTGAGGCACAAGAA | 59349 |
rs557753328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899866 | AAATAAAAAAATCAA[A/G]GCATAAGAATGAAGG | 59349 |
rs557764307 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202915100 | ATAGATTTTCTCCAC[A/T]ATACATTTTCACAAA | 59349 |
rs557818049 | snp | C/T | | | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202930588 | GTATACTTTTAGTTA[C/T]TTTAAAATGTACAAT | 59349 |
rs557829064 | in-del | -/A | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911410 | TAGTCAATTTGGGTT[-/A]AAAAAAAAAATATAT | 59349 |
rs557843302 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202907265 | CTTCTCTGTATTTCT[A/G]CAAGTTCTACATTGA | 59349 |
rs557888228 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928871 | CTCTTGCTCTGTCGC[C/G]GAGGCTCGAGTGCAC | 59349 |
rs557960444 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL12 | GRCh38.p7 | 1:202910053 | CAAGAAGTTCTTAGT[C/T]GAACTGGAAAGGAAA | 59349 |
rs558037510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901392 | TACCTCCCAGGCTCA[A/G]GCAATCCTCCTACCT | 59349 |
rs558107582 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897420 | TGTATTTTTAGTAGA[C/G]ATGGGGTTGGTCAGG | 59349 |
rs558343647 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202901673 | TTCTTTGCTGTGAAG[C/G]ACTCTCTTCATTATT | 59349 |
rs558360725 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202922501 | AAGACTTTTTTTTTT[C/T]TTTGAGACAGAGTCT | 59349 |
rs558371009 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925800 | TCCAAACATATCTGG[A/C]TTTCTTCTTAAAATG | 59349 |
rs558538889 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | KLHL12 | GRCh38.p7 | 1:202904770 | GAAATAAGGCAGATG[A/C]AGGACTGCTAAAATA | 59349 |
rs558562529 | snp | A/G | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892302 | AATGTGGTCTCTCAC[A/G]TCCATTCAATGTGCA | 59349 |
rs558631959 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202914285 | GTTAGATGCTGCTCT[G/T]GTACATTAGGCAAAA | 59349 |
rs558817679 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202896403 | ACCATATTGCCCAGG[A/C]TGGTCTTGAACTCCT | 59349 |
rs558875196 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911417 | ATTTGGGTTAAAAAA[A/T]AAATATATATATATA | 59349 |
rs558909667 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202918445 | CAGGTGTGATCTAGG[A/C]TATATTCTTGTATCT | 59349 |
rs558915601 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202917977 | CCACTGGGATCATAT[A/G]TCTAATTGAAGAAAG | 59349 |
rs559054871 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202916274 | CTACAGTTGGAACCA[A/G]TGTGACCAATGTGCT | 59349 |
rs559115326 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892059 | CCCTAGCTACCTGTA[G/T]ATGAGAAAATGTAGT | 59349 |
rs559125491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912442 | TCGTGGAGGTGGTTT[C/T]GGTTGGCATGACAGC | 59349 |
rs559137185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202910454 | TTGTAGTTAACTAAG[A/G]GATCTAGGGCTGGGC | 59349 |
rs559151960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899604 | GCCAAAGCAGGTAAA[C/T]TGTCTGAGGTCAGGA | 59349 |
rs559170364 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KLHL12 | GRCh38.p7 | 1:202917228 | TATTCCTTCTTCCCC[C/G]GCAAGAGACAGGGTC | 59349 |
rs559261851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924668 | AGAAATAGTAAAATC[C/T]AATAGCTGACATGTG | 59349 |
rs559312215 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927806 | CCAACATGGTGAAAC[C/T]CTATCTCTACTGAAA | 59349 |
rs559347686 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920521 | AGTTTGGACTACAGG[A/C]GCCCGCCACCACGCC | 59349 |
rs559390540 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905957 | CTACAGGTGCCCGCC[A/C]CCACACCTGGCTTTT | 59349 |
rs559430202 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920354 | AAAAAATAAAATTAT[G/T]CTCTATTTTGTTGGA | 59349 |
rs559466552 | snp | A/T | 0 | 0 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919687 | TTCATGATTAAGTTT[A/T]CACTATTAATTTTCA | 59349 |
rs559597037 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202924575 | GACCAGCGTGGGCAA[C/T]ATAGTGAGACCCTGT | 59349 |
rs559599559 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913137 | ACGCACTATGCTATT[A/T]GAGAAGATATATTTA | 59349 |
rs559743261 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928031 | ACGCCTGTAATCCCA[G/T]CACTTTGGGAGGCCG | 59349 |
rs559765383 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911925 | CTATTTTGAGCAATG[C/G]GGAATGCTCACGGAC | 59349 |
rs559770871 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897830 | CTGCCTCAGCCTCCC[A/G]AAGTGCTGGGATTAC | 59349 |
rs559865382 | snp | C/G | | | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929880 | CTGGGCACAGTGGCT[C/G]ACGCCTGTAATCCTA | 59349 |
rs559883940 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926534 | TTAAGTCAACTTAGT[G/T]GCAACTCTAGGGGTG | 59349 |
rs559919651 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901554 | CGATGCTTCTGCTTC[A/G]GCCTCCCAAAGTGCT | 59349 |
rs560001637 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | KLHL12, RABIF | GRCh38.p7 | 1:202890977 | GGCTACCTCTTACCT[A/G]TGTCTAACATAGAAA | 59349 |
rs560036577 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202899142 | ACAAGGCAAAACCCC[A/G]TCTCTACTAAAAATA | 59349 |
rs560048666 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202902302 | AGACATGGTAGCACA[C/T]GCCTGTAATCTCAGC | 59349 |
rs560196474 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908029 | TCAGATAAAAGGAAA[A/C]AATAAAACAAAATAC | 59349 |
rs560220069 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893873 | TGAAGGTAAGTAGCT[A/T]CTCTTTTGTCCTTAT | 59349 |
rs560353335 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914470 | AAATAGTTTTAAGCA[C/G]ATACATGATAGACTC | 59349 |
rs560429352 | in-del | -/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911771 | CTGCCTGTGGACGCC[-/G]CCGAAGAAGCATCTT | 59349 |
rs560583757 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928350 | GGGTCCGGCAGGGAG[C/G]CTGGGAATGTATCTA | 59349 |
rs560645082 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901938 | CCATCCCCACTCACG[-/T]TATTACCCCTCCCTG | 59349 |
rs560769620 | snp | C/T | 7.89578e-05 | 0.00628273 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925231 | GGGAAAAAAAAACAA[C/T]GAGCATATTCAAAGA | 59349 |
rs560785370 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911963 | TAATGAGAGACCCAA[A/C]CACCAAGTGCTCCAG | 59349 |
rs560821155 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918986 | CCAGGAACGGTGGCT[C/T]GTGCCTATAATTCCA | 59349 |
rs560859667 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202918303 | CAGGTCAACACAATT[A/G]TGGGTTTCAGCAAAA | 59349 |
rs560886645 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911778 | TGGACGCCGCCGAAG[A/G]AGCATCTTTAAAGTC | 59349 |
rs561180743 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202917964 | TAGTGATTCTTACCC[A/T]CTGGGATCATATATC | 59349 |
rs561245809 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925875 | CTTTAGGAGGCTGAG[A/G]TGGGTGATCAGTTGA | 59349 |
rs561301168 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909701 | GAACTGTGTCAATAG[C/G]GCTTCCTATGCCTTC | 59349 |
rs561343850 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896457 | CAGCCTCCCAAAGGG[C/G]TGGGATTATAGGTGT | 59349 |
rs561699118 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906707 | CACTCTGTCGCCCAG[A/G]CTGGAGTACAATGGT | 59349 |
rs561939116 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL12 | GRCh38.p7 | 1:202892806 | GGCAACATGGTGAGA[A/C]CCTGTCTCAATAAAA | 59349 |
rs561975151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900119 | ATGTATGAATAAAAA[C/T]TCCCACACCAACCAA | 59349 |
rs561989791 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907911 | GACCTCATTTCTATT[-/A]AAAAAAAATAAAATA | 59349 |
rs562101014 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906040 | TAGCCTGGATGGTCT[C/T]GATCTCCTGACCTCG | 59349 |
rs562133886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202898858 | ACAAACAACAAAAAA[C/T]TATGGAAAAAAAATT | 59349 |
rs562172214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905883 | GATCTCAGCTTACTG[C/T]AGGCTCCATCTCCTG | 59349 |
rs562201097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202902417 | CCTGGGTAACAGAGC[A/G]AGACTCCGTCCAAAA | 59349 |
rs562228567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202927016 | GGAGACCAAGGATGG[A/G]GGGTAGGGCCATAAC | 59349 |
rs562354279 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927327 | GTGAGGAGGTGGTGT[C/T]ACGTGACCTGTCTGT | 59349 |
rs562369125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895427 | ACCTTAATTTTTTCT[C/T]CGTATTTCATGCTCC | 59349 |
rs562566041 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894863 | GCAAAAACAAAGTAT[A/T]TTTAAATGAGATAAG | 59349 |
rs562656502 | snp | A/G | 8.24083e-05 | 0.00641852 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202911153 | CCGCTCTTTCTTGGC[A/G]TGCTTCACCCAGTTG | 59349 |
rs562737659 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901637 | AAATGGCTGGGATCC[C/T]TCGATCACTGATTCC | 59349 |
rs562757079 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202908363 | AATAGCTAATACACA[C/T]AGTTATTATGTGCCA | 59349 |
rs562773357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908908 | AGAAAAGGTCTGAAA[C/T]GAGGTGTCTGTACTT | 59349 |
rs562783253 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923165 | GTTTTTAAAGAAAGA[A/C]ATCATCACTGATGAG | 59349 |
rs563048767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922371 | AGGATATCGAGACCA[C/T]CCTGGCTAACATGGT | 59349 |
rs563139853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202898906 | TAAGGAATTGTGTGA[C/T]TTTAAACAGTGATAA | 59349 |
rs563176698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905950 | GCTTGAACTACAGGT[A/G]CCCGCCACCACACCT | 59349 |
rs563353806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925939 | GTGAAACCTAGTCTC[C/T]ACTAAAAATACAAAA | 59349 |
rs563383771 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926895 | GGTGGAGGTATCGGA[A/G]AGGGGCAGTTCAGGG | 59349 |
rs563390506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925315 | CTTCCTCAGACCCAA[A/G]CATACACAAGTTGAG | 59349 |
rs563439812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912016 | GCCATTGTGGAGGAG[A/G]TGGATGCAGCCATGA | 59349 |
rs563565559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912397 | CATCCAGCCAAAGAA[A/G]TCGAAGTGGTTCTGG | 59349 |
rs563604446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919665 | TCCATAGTTTGTCTC[C/T]AAAATGTTCATGATT | 59349 |
rs563637684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202917578 | CTCACAAGACAGTTA[C/T]GATTTGGCTCCTGCT | 59349 |
rs563668342 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | KLHL12 | GRCh38.p7 | 1:202904192 | TATTTTTAGTAGAGA[A/C]AGGATTTCTCCATGT | 59349 |
rs563699675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896515 | GAGCTCAACTGAACA[C/T]TGGGTTCAATTCAAC | 59349 |
rs563706928 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202903533 | GGTGCAATTATGGTT[C/T]ACTGCAGCCTCAGCC | 59349 |
rs563707044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911506 | TACCTAATAAATCAC[C/T]AGTCACGTATTGGCC | 59349 |
rs563743878 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202910883 | ACTTGCCAAGAAATT[C/T]GCTTTTCTTAGAAAT | 59349 |
rs563775912 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904895 | CTTTGAGACAGTAAT[A/G]GGTAAGGTTAATAAC | 59349 |
rs563790221 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897150 | GAGGCTGTAGCTCTC[G/T]AGTCTCTGAAACTTA | 59349 |
rs563915705 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202892849 | AAGAAAGAAATTAGC[A/C]TTCTATTCCTTTCCA | 59349 |
rs563991411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914349 | GTGGTGAGCCACTGG[A/G]GAAATACTTGGGAAG | 59349 |
rs563993670 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202923899 | AAAAACTTGTGCTTA[A/G]AAAGACTTTTAAAAC | 59349 |
rs564061945 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900777 | GGTGAGGCACGAGAA[A/T]CGCTTGAACCTGGGA | 59349 |
rs564097105 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900166 | TATGCAAATTTTAAA[C/G]TTTTCTATTGATTTT | 59349 |
rs564116928 | snp | C/G | | | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929078 | TCGTGATCCGCCCGC[C/G]TTGGCCTCCTAAAGT | 59349 |
rs564178392 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202902909 | AGGCTGAGGTGGGAG[A/G]ATCACTTGAGTCCAG | 59349 |
rs564211502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913937 | GCTAGCGGGAGCAAA[C/T]CAGACACTATAGATA | 59349 |
rs564385188 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B | KLHL12, RABIF | GRCh38.p7 | 1:202891115 | TTAGCCACAAACTCT[C/T]GGCATTTGAGACCGT | 59349 |
rs564418938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928254 | TACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTCC | 59349 |
rs564528006 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891927 | TAATTCTAACTTCAA[C/T]TCTGATATACAAATC | 59349 |
rs564593442 | snp | A/G | | | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202918300 | CATCAGGTCAACACA[A/G]TTGTGGGTTTCAGCA | 59349 |
rs564602986 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920525 | TGGACTACAGGCGCC[C/T]GCCACCACGCCCGGC | 59349 |
rs564643062 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900374 | CATGGTGAGACTCCC[A/G]TATCTAGAAAAAAAT | 59349 |
rs564750439 | in-del | -/TTTAACCC | 0.00279162 | 0.0372561 | intron-variant | KLHL12 | GRCh38.p7 | 1:202903959 | TTACACACAAATGGT[-/TTTAACCC]TTTAACCCTTTATCT | 59349 |
rs564815058 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202925085 | GGTATTGCTCTTCCT[A/G]AGGGAGTTCATTGAA | 59349 |
rs564851439 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924398 | TGTGGTTTGAATCCT[A/T]CTCCTCTCTCCTTCC | 59349 |
rs565126116 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895469 | AGGAGAGGTTAAAAA[C/G]CCTGGTCCAGCCACA | 59349 |
rs565363072 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929973 | AACGTGGCAAAACCC[C/T]GTCACTACTAAAAAT | 59349 |
rs565408561 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909570 | AGGTTCACAGTCCTG[C/T]TGTAATTACCATTGT | 59349 |
rs565442620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202916124 | ATGCCTGCCACTTCA[A/G]CACAAGGATACAATG | 59349 |
rs565534035 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202893546 | AGGGATATGGAATGG[A/G]CCCACACGGGCCTAG | 59349 |
rs565567974 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891328 | GCTCAGAAATGTTGA[C/T]AGCTGAGGTACTGAA | 59349 |
rs565595849 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202897732 | GTGATGGATTTAAAA[A/T]CTCTTTTTCTTTTTC | 59349 |
rs565604851 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | KLHL12, RABIF | GRCh38.p7 | 1:202890755 | TTTTGCAGGCCTTCC[A/G]CATAGCTGTTTATAT | 59349 |
rs565605152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202898973 | CTTTTAGAGACACAC[A/G]TGGAAGTATGACACA | 59349 |
rs565617534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202904873 | AAAGTAATTTCCATT[A/G]TATCTTCTTTGAGAC | 59349 |
rs565641219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202898408 | AAACACAGATAAACC[C/T]CTAATGAAGTAATGG | 59349 |
rs565649670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911770 | TCTGCCTGTGGACGC[C/T]GCCGAAGAAGCATCT | 59349 |
rs565745803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912158 | GCAGCATTAAAGAAG[A/G]CACTGAAGAACATCA | 59349 |
rs565929019 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919690 | ATGATTAAGTTTACA[A/C]TATTAATTTTCAACC | 59349 |
rs565930511 | in-del | -/AA | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202907612 | TAAAAAAAAAAAAAA[-/AA]GGAAAAAAATTATAT | 59349 |
rs566027420 | in-del | -/TATC | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202903992 | ATCTATCTATCTATG[-/TATC]TATCTATCTATCTAT | 59349 |
rs566183122 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896031 | CTGGGCTAAGAGACT[A/G]ATATCCTTCCATAAA | 59349 |
rs566258702 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202894578 | TCCCATTCCTGCATC[C/T]CAGACTCAATACCTA | 59349 |
rs566401401 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924670 | AAATAGTAAAATCCA[A/C]TAGCTGACATGTGTG | 59349 |
rs566532147 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893022 | TGGCACAGTGGCGTG[A/C]ACCTGTGGTCCCAGC | 59349 |
rs566577155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920577 | GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 59349 |
rs566614020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920109 | ACCTGAGGTCAGGAA[C/T]TCAAGACCAGCCTGG | 59349 |
rs566756893 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922087 | AATTTCTCATTCAAT[A/G]AACTACATTTCCATC | 59349 |
rs566795540 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921375 | AGATGGGGTTTCACC[A/C]TGTTGGCCAGGCTGG | 59349 |
rs566797048 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202915511 | TTCTCAAGCTGTTTT[C/T]CATTTAAGCTTCTAA | 59349 |
rs566949246 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900341 | TTGCGCCCAGGGGTT[C/T]GAGGCCACTTTGGGT | 59349 |
rs566972127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202917879 | GTGAAATGAGTGAAC[A/G]GGTAATAGAGAAGTG | 59349 |
rs566987862 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907292 | TTGAACATGCAGTAC[G/T]TATGCCATTAAAAAA | 59349 |
rs567005990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202916838 | TTAAAAAATTAGCCC[A/G]GTGTGGTGATGTGCA | 59349 |
rs567065072 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892419 | TCACTGCACTGGTGC[C/T]TGTAATCACCCGGTG | 59349 |
rs567125273 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906792 | TCAGCCTCCAGAGTA[G/T]CTGGGATTACAGGTG | 59349 |
rs567158391 | in-del | -/CT | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202909773 | CTCTCAAGGCAGTGA[-/CT]CTACACGATTCTCTT | 59349 |
rs567249928 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202906688 | TATTTTTGAGATGGA[A/G]TCTCACTCTGTCGCC | 59349 |
rs567324030 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202912260 | GAAAAGGGGCTTTGC[C/T]TTTGTAACCTTTGAT | 59349 |
rs567450404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897305 | CAATTCCATGATCTC[A/G]GCTCACCACAACCTC | 59349 |
rs567589931 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901996 | TGTGATTATAAAACA[C/T]ATAATATACATTTTT | 59349 |
rs567628169 | snp | A/G | 1.64982e-05 | 0.00287208 | missense | KLHL12 | GRCh38.p7 | 1:202909115 | ATTGTAAACTACAGC[A/G]GATGAAAGGCTGAAA | 59349 |
rs567723778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901187 | TCCTGTTGGCTGAAA[C/T]TTTCCCAATAAACAC | 59349 |
rs567762139 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908448 | TACAGGCAGGTGCTA[C/T]GATGATTCCATTTAC | 59349 |
rs567769716 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202915578 | TTTTATTCCAAAGCC[G/T]GTATAGTTCCAAAAG | 59349 |
rs567857025 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202918978 | ACTGGGGACCAGGAA[C/T]GGTGGCTCGTGCCTA | 59349 |
rs568036296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202898593 | AGCCTCTAATCCAAC[C/T]ACTAGTTTACAGGCA | 59349 |
rs568047261 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891519 | TGGGGCAGTAATCAG[A/G]TAGCTGAACTACTAG | 59349 |
rs568168182 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905673 | TTTCTTTGCACAACT[A/C]TTTGCGCATCCCTAA | 59349 |
rs568204330 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927773 | TTACTTGAGGTCAGG[A/G]GTTCGAGACCAGCCT | 59349 |
rs568222149 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892173 | GCCCATATCTAGTAG[C/G]CTATACTCACCTTAG | 59349 |
rs568234375 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202903074 | GCTGAGGTGGGAGGA[C/T]TGCTTGAGCCCAGAA | 59349 |
rs568240120 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927361 | CTAGCGCGGGGCTTC[C/T]GTACGCTGCTAGGAA | 59349 |
rs568257240 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime | KLHL12 | GRCh38.p7 | 1:202927208 | CCAGACCCGGAGGCT[C/G]TGGAGGCTCTGGAGC | 59349 |
rs568392113 | in-del | -/T | 0.291493 | 0.246533 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921178 | ACTACAACCAGCTAA[-/T]TTTTTTTTTTTTTTT | 59349 |
rs568557391 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202930205 | TTCCTTGTTTTCAGG[A/T]TGTAAAATAGTACTT | 59349 |
rs568789703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922129 | ATATGGAAACAATTT[C/T]ACTATGTAAGAACTT | 59349 |
rs568992510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913719 | AGCAACAAATTGAAA[C/T]CTGATGGATGAGTAG | 59349 |
rs569015098 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202903992 | TATCTATCTATCTAT[C/G]TATCTATCTATCTAT | 59349 |
rs569038071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202915662 | CATGACGAGCTCATA[A/G]TTGAGTGATTAAGAG | 59349 |
rs569114956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909289 | GCTCTCGGTTTCCAG[A/G]AATGATTTTTAAAAT | 59349 |
rs569216953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907466 | AATTAGCCAGGGATG[A/G]TGGCAGTCGCCTGTT | 59349 |
rs569234809 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921199 | TTTTTTTTTTTGACA[A/C]AGTCTTGCTCTGTTG | 59349 |
rs569350216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893931 | TTATTAAGCATGTAC[C/T]ACACAGGCAAAATTG | 59349 |
rs569353267 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920736 | GCTTTCCAAATGAAG[C/T]AGGTAGTTATCTATA | 59349 |
rs569353755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202903851 | TGGTCTCGAATTCCT[A/G]GGCTCCATCGCCTGC | 59349 |
rs569386455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901005 | GAGCCGAGATCATGC[C/T]GCTACACTCCAGCCT | 59349 |
rs569392896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911387 | GCTAACAGACCAGGA[A/G]AAGAATTATAGTCAA | 59349 |
rs569506877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202900378 | GTGAGACTCCCATAT[C/T]TAGAAAAAAATAATA | 59349 |
rs569578089 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897338 | CCTCCTGGGCTCAAG[G/T]GATTCTCCTGCCTCA | 59349 |
rs569581488 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904951 | TTTTAACTTGGCTGT[C/T]AATTTAATTTCCTTC | 59349 |
rs569619188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202904745 | GTGTGTGCTGTGACA[C/T]GTTGTTAGAGAAATA | 59349 |
rs569642674 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202907420 | CAGCCTGGTCAACAT[C/G]GAGAAACCCTGTCTC | 59349 |
rs569674182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911689 | CTCAAACTGTTCACC[C/T]AAGCCTCTGAAGCAG | 59349 |
rs569789933 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920655 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 59349 |
rs569822536 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | KLHL12, RABIF | GRCh38.p7 | 1:202890639 | GGTTTAATTAGCATG[C/T]ACAATCCATCTGCCA | 59349 |
rs570065414 | snp | C/G | 5.00204e-05 | 0.00500077 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919939 | GTATAAAAGAATGAT[C/G]GTTATAATTCCACAA | 59349 |
rs570067656 | in-del | -/CA | 0.00318978 | 0.0398085 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919084 | GAGAGAACTCATCTC[-/CA]CACAAAAAAATTTTG | 59349 |
rs570136869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202902773 | AGCAGGCAGATCACA[C/T]GAACCCAGGAGATCA | 59349 |
rs570166241 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202902152 | AAACACAAATGGGGG[A/C]CGGGCACAGTGGCTA | 59349 |
rs570315783 | snp | A/C/T | | | missense | KLHL12 | GRCh38.p7 | 1:202925153 | CTTTGGGGGCCATAA[A/C/T]GCCTCCCATAAAGCA | 59349 |
rs570319563 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923762 | CAACAATTACTAGCA[C/G]AGTACCTGGCCCATA | 59349 |
rs570380120 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202896429 | CTCCTGGCCTCAAGA[C/G]ATCCTCCCATCTCAG | 59349 |
rs570526325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899768 | GAAGAGGTTGCAGTG[A/G]GCCGAGATTGCACCA | 59349 |
rs570602915 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202926283 | AGAATCGATATTGGA[A/T]TCCAAAACTTTCTGA | 59349 |
rs570708802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919386 | AATACTACCACTTAA[C/T]GGCCAGATAGATAAA | 59349 |
rs570713829 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925815 | ATTTCTTCTTAAAAT[A/G]AAACTTCAGGCCGGG | 59349 |
rs570747235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920822 | TAACTTTAAAAATCT[A/G]TTTCATATTAAAATA | 59349 |
rs570947079 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922648 | CCCGCCACCACGCAC[A/G]GCTAATTTTTTGTAT | 59349 |
rs570998262 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922647 | GCCCGCCACCACGCA[C/T]GGCTAATTTTTTGTA | 59349 |
rs571071312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912206 | ACAGTTTGGAAAAAC[A/G]GAAGTGATTGAAATC | 59349 |
rs571105734 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912597 | ATTTTGGACCCATGA[A/C]GGGAGGAAACTTTGG | 59349 |
rs571141478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919999 | TTAGAGATGTTAATA[A/G]TATTAATTGAACATT | 59349 |
rs571205784 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893107 | TAAAAAAAATCTAAT[-/A]AAAAAAATCAAGTTG | 59349 |
rs571220335 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202916661 | TATATTACACAAATA[A/T]CCTAGTTTTAACAAA | 59349 |
rs571429584 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202910017 | CAGCTCTAATTAAAT[C/G]GCACCTCTATTAACC | 59349 |
rs571532475 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894942 | AACAAAATCCTTAAA[A/C]GCATTCAAAGACCAC | 59349 |
rs571545319 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929650 | TTTTTGCTCTTTGTA[A/T]TTTATTTTGCCTTTT | 59349 |
rs571576432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894107 | CATTAATCTACGGTT[C/T]GTCCCATGCACCACC | 59349 |
rs571627505 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914638 | TTTGGGAGGCCGAGG[C/T]GGGTGGATCACGAGG | 59349 |
rs571727491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202914158 | CTCTCAGAGCAACTT[A/G]AAATCATCCGAAGGT | 59349 |
rs571749639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897444 | GGTCAGGCTGGTCCC[A/G]AACTCCCAACCTCAA | 59349 |
rs571845482 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202921235 | GCTGGAGTGCAGTGG[C/T]GTAATCTTGGCTCAC | 59349 |
rs571853745 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | KLHL12, RABIF | GRCh38.p7 | 1:202890934 | TCAGGTAAATATTTT[A/G]CTGATGAGAATCTCC | 59349 |
rs572043272 | snp | A/C/G | 3.29464e-05 | 0.00405861 | missense | KLHL12 | GRCh38.p7 | 1:202925089 | TTGCTCTTCCTGAGG[A/C/G]AGTTCATTGAATTGA | 59349 |
rs572336944 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202917740 | ACATTTTTTTTGTCT[A/G]TATCTCTGTCTCTAC | 59349 |
rs572532606 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202904519 | CAATCTGACTCGTGT[-/A]AAAAAAAAGCTAGTG | 59349 |
rs572569999 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202923020 | CCCAGTGAAGTTAGA[C/T]GGTTCCCAGGGTTTA | 59349 |
rs572598172 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202903351 | TTATAACTAATAAGA[A/C]CCTATTATTAATTAG | 59349 |
rs572635664 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202910458 | AGTTAACTAAGAGAT[C/G]TAGGGCTGGGCCAGC | 59349 |
rs572705950 | in-del | -/A | 0.00755907 | 0.0610114 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896196 | AGACAGATACAAACT[-/A]TTTTTTTTCTGAGTT | 59349 |
rs572762673 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918001 | AAGAAAGTGGCAAAC[C/T]CCCTCTCCATAAAAA | 59349 |
rs572887077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202904166 | TGTGCCACCAAGCCC[A/G]GCTAATTTTGTATTT | 59349 |
rs572890227 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202923103 | CTTTGAACAATTACT[C/T]TCAAAAATAAAGACA | 59349 |
rs572972283 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920368 | TGCTCTATTTTGTTG[A/G/T]ATTTTTTTTTTTTTT | 59349 |
rs572988621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202912327 | TACCATCCTACGAAT[A/G]GCCATAACTGTGAAG | 59349 |
rs573031944 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202907286 | TCTACATTGAACATG[C/T]AGTACTTATGCCATT | 59349 |
rs573238090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905851 | ACTCTGTCGCCCAGG[C/T]TGGAGTGCAGTGGCG | 59349 |
rs573280263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911937 | ATGGGGAATGCTCAC[A/G]GACTGTGTGGTAATG | 59349 |
rs573423334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202915982 | ATTAGCTATTATATG[C/T]AGTGAACGTCAAATC | 59349 |
rs573465418 | snp | C/T | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892387 | GACGGGGAGTATGTG[C/T]CAAATAAGTACAATC | 59349 |
rs573510592 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891792 | TGCTGTCTCCAGTGC[A/G]AAAGACCTCGGGGAA | 59349 |
rs573600040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202902344 | CTGAGGCAGGAGAAT[C/T]GCTTGAACTTGGGAA | 59349 |
rs573767086 | snp | C/T | 1.65201e-05 | 0.00287398 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202893380 | GCTGTACCATCAAAT[C/T]CCCCCACCACATAAA | 59349 |
rs573852937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202915228 | TGAAAATTAGTGGTT[A/G]GGTAACACATGCCAC | 59349 |
rs573864172 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895308 | TGAGGTGGGAGGATC[A/G]CTTGAGCTTGGGGAG | 59349 |
rs573885376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202903093 | TTGAGCCCAGAAAGT[A/G]AAGTTTCAGTGAACC | 59349 |
rs574015398 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202902169 | GGGCACAGTGGCTAG[C/T]GCCTGTAATCCCAGC | 59349 |
rs574046179 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913476 | ACCCCACTCTTAACT[G/T]CCAGGCACTGTCCTG | 59349 |
rs574136835 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922765 | TGCTGGGATTACAGG[A/C]GTGAGCCACCACGCC | 59349 |
rs574218697 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929819 | GTAGCAAGAGCACGC[A/C]TCAAAATATATTTAT | 59349 |
rs574245939 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922322 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG | 59349 |
rs574308981 | in-del | -/A | 0.00755907 | 0.0610114 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925433 | TCACGGAGTGTCCCT[-/A]CCACTTGACATTTAA | 59349 |
rs574318526 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925884 | GCTGAGGTGGGTGAT[C/G]AGTTGAGGTCAGGAG | 59349 |
rs574410679 | in-del | -/A | | | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928312 | AAAAAAAGAAAAAAC[-/A]AAAAAAAAGGCTGGA | 59349 |
rs574481959 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202925968 | AAAATAGCCAGGCGT[A/G]GTGATGCGCGCCTAT | 59349 |
rs574502509 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920187 | GGCATGGTGGCACAT[A/G]CCTGTAGTCCCAGCT | 59349 |
rs574597540 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901059 | AAAAATAAAATAAAG[-/A]AAAAACCCCTCTCTT | 59349 |
rs574669876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919537 | GAAAAGGTGCAAATG[C/T]TCTCTTTTATAGAGC | 59349 |
rs574706807 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202926600 | AGACAGCCCGGGGGG[A/T]CTTTTATCGTTTCCG | 59349 |
rs574842739 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918132 | AGTTTTGTAATTGCC[C/G]AATCTTGAAGAAACC | 59349 |
rs574867610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924044 | CTGCTCTTAAAATGA[A/G]ACTTGGGATCTTGAA | 59349 |
rs574964832 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928699 | CTAATTGATTCAGGA[A/C]ATTCTAATTTATTTT | 59349 |
rs575022942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202904988 | ATGCAGAAGAGTCAT[C/T]ATCCTGGTAGCTGGT | 59349 |
rs575065410 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904433 | CTATTTTGTGCCTAG[A/G]AAGTCCTTCTTCCCC | 59349 |
rs575170217 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202893496 | ATAGAAATAAACTAC[A/G]GTCACTAATGACTAG | 59349 |
rs575196862 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202897575 | GACATAATCCTTGAG[A/G]TCTTAAGTGCAGGTG | 59349 |
rs575240393 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921524 | TGCAGGTCATCCTAA[A/G]GGACTTTCTTATGTA | 59349 |
rs575290556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913925 | CAGCAACACGGGGCT[A/G]GCGGGAGCAAACCAG | 59349 |
rs575301485 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202926038 | TGAACCCAGGAGGTG[A/G]AGGTTGCAGTGAGCC | 59349 |
rs575313738 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906316 | AAAAATTAGCCAGGC[A/G]TGGTGGCACACACCT | 59349 |
rs575317411 | snp | A/C | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB, missense | KLHL12 | GRCh38.p7 | 1:202927505 | CTGGGGATCACGGCA[A/C]AACCCCGTTTCTACA | 59349 |
rs575325373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202920968 | GGTTATAACTCCAGT[C/T]TCTCCAGGACTACCT | 59349 |
rs575350095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202905947 | GTAGCTTGAACTACA[A/G]GTGCCCGCCACCACA | 59349 |
rs575436413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893531 | GTTCTACAGTAGATG[A/G]GGGATATGGAATGGG | 59349 |
rs575551138 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202901267 | ATGTATAAAGGAGTT[C/T]GTTTTGTTCTGTTTA | 59349 |
rs575587961 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908538 | ACGAGGTAAACTGGT[A/C]CCTGCACCAACAGTA | 59349 |
rs575712218 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL12 | GRCh38.p7 | 1:202903126 | GATCATGCCACTGCA[C/T]TCTAGCCTAGGAGCC | 59349 |
rs575749382 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202910302 | TCTGTGCTCCTAAAC[A/T]CAATGTAAAGAACTA | 59349 |
rs575751252 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | KLHL12 | GRCh38.p7 | 1:202902440 | GTCCAAAAAAAAAAA[A/C]ACCAAAAACAAACAA | 59349 |
rs575765891 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202899075 | CCCAACACTTTGGGA[A/G]GCCAAGGCTGGCAGA | 59349 |
rs575796868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924866 | CAAAACATCACACTG[C/T]AAAAATTCAAAATTA | 59349 |
rs575857304 | snp | A/T | 0.0298908 | 0.118541 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899850 | AAAAAATAATAATAA[A/T]AAATAAAAAAATCAA | 59349 |
rs575896487 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891879 | TCAGTGCTGTTCTAG[A/G]TTCACTCACAATCAA | 59349 |
rs575993100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896326 | AAGTAGCTAGGACTA[C/T]AGGCATGCACCACCA | 59349 |
rs576150809 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL12 | GRCh38.p7 | 1:202917975 | ACCCACTGGGATCAT[A/G]TATCTAATTGAAGAA | 59349 |
rs576184688 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909461 | AAACACAAGTACATA[A/G]TAACTAATAAGAATT | 59349 |
rs576190340 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202920100 | AGGCAAATCACCTGA[C/G]GTCAGGAATTCAAGA | 59349 |
rs576502580 | snp | A/G | 0.00676609 | 0.0577691 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929911 | ACACTTCGAGAGGCC[A/G]AGGCGGGCGGATCAC | 59349 |
rs576534286 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KLHL12 | GRCh38.p7 | 1:202917007 | AAAGAATTGGACCAC[C/T]GGAGATCAATACTAT | 59349 |
rs576565346 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202920431 | TCCCAGGCTGGAGTG[C/T]AGTGGTGCCATCTCG | 59349 |
rs576581677 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906490 | AAAAAGTTCCTACCC[C/T]GGGAGGAAAGGCAAA | 59349 |
rs576624765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202922644 | GGCGCCCGCCACCAC[A/G]CACGGCTAATTTTTT | 59349 |
rs576669143 | in-del | -/GTTCAAGT | 0.00557542 | 0.0525036 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921106 | ACCTCTGCCTCCCAG[-/GTTCAAGT]GTTTCTCGTGCCTCA | 59349 |
rs576726932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919677 | CTCCAAAATGTTCAT[A/G]ATTAAGTTTACACTA | 59349 |
rs576755214 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899997 | TTCCCTACCTATTCC[-/T]TTTTCTTACTCCACC | 59349 |
rs576907703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202926784 | TCGGGAGATTCGGGG[C/T]AGGGAATGGGTAGTA | 59349 |
rs576914558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913766 | GTAAGAGAGTACTCC[A/G]AGGCAGACAGAAGAG | 59349 |
rs576951592 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925697 | GTAAGAAAAAGTGTG[A/T]ATTCAACTTCAACTT | 59349 |
rs577057378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202913085 | AAACAAGAAAGAAAA[A/G]CATTATCAATTAGCC | 59349 |
rs577120654 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911901 | AACCAATGAAGAAAG[C/G]CTGAGGAGCTATTTT | 59349 |
rs577294545 | snp | A/G | 6.59413e-05 | 0.00574163 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202918180 | CCGTACCTGAATTTC[A/G]TCGCACTTGATTAGC | 59349 |
rs577519655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908684 | TTACCTGCCATTATG[C/T]GGCACTAAAATTATC | 59349 |
rs577536834 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926474 | GCAAGACCCATTTTA[C/T]AGAAAAGCGGGTGAT | 59349 |
rs577593563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897823 | GATTCTCCTGCCTCA[A/G]CCTCCCAAAGTGCTG | 59349 |
rs577651821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202907996 | ACTAACACCTTAGCA[C/T]GCATCATGAGTCCTC | 59349 |
rs577652971 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202915102 | AGATTTTCTCCACAA[C/T]ACATTTTCACAAAGA | 59349 |
rs577696550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899935 | ATTACTTCAAGTTGG[C/G]AGAAGCTAGGACCAC | 59349 |
rs577731591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202899572 | GGCTCATGCCTGTAA[C/T]CCTAGCACTTTGGGA | 59349 |
rs577778366 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL12 | GRCh38.p7 | 1:202921778 | ATCTTAATCTTAGTT[C/T]AGAAATTCATTTTAC | 59349 |
rs577916674 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928896 | GTGCACTGGCGCGAT[C/T]TCAGCTCACTGCAAC | 59349 |
rs577981515 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202902285 | AAATACAAAAATCAG[C/G]CAGACATGGTAGCAC | 59349 |
rs578043946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL12 | GRCh38.p7 | 1:202906988 | TTTTACAAAAAAGAA[A/G]AAAAAGACTTCCATC | 59349 |
rs578046875 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202902057 | GTATTATGAAAAAAA[A/T]ATTACCCATAGTTCC | 59349 |
rs578063185 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202913762 | GGGAGTAAGAGAGTA[C/T]TCCGAGGCAGACAGA | 59349 |
rs745315081 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202906718 | CCAGGCTGGAGTACA[A/G]TGGTGCAATCTTGGC | 59349 |
rs745315223 | in-del | -/CAG | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202919148 | GTGGTCCCAGCTACT[-/CAG]GAGGCTGAGGTGTGA | 59349 |
rs745316448 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202921121 | GTTCAAGTGTTTCTC[A/G]TGCCTCAGCCTCCCA | 59349 |
rs745336661 | snp | C/T | 1.64795e-05 | 0.00287045 | missense | KLHL12 | GRCh38.p7 | 1:202911142 | AAGGATTCTTCCCGC[C/T]CTTTCTTGGCATGCT | 59349 |
rs745520626 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202919953 | TGGTTATAATTCCAC[A/G]AGATAAAGGCAGAAT | 59349 |
rs745656039 | snp | A/G | 1.70464e-05 | 0.0029194 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895507 | GGAAATAATTGCCCT[A/G]CACATCCAGCCTACC | 59349 |
rs745682143 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202915420 | GAACAGAAAAATATA[C/T]GTCACTTGCTTTCTT | 59349 |
rs745720689 | snp | C/T | 1.65094e-05 | 0.00287305 | missense | KLHL12 | GRCh38.p7 | 1:202894702 | CATAGCGCTCCATAC[C/T]GGTGTGACGCCTGCT | 59349 |
rs745747601 | snp | C/T | 1.64784e-05 | 0.00287035 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202919843 | GTACACAAAGTCCAA[C/T]AAAATTTCCATGGTA | 59349 |
rs745796879 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202893080 | ACAGAGCAATACTCT[A/G]TCTCTAAAAAATAAA | 59349 |
rs745808815 | snp | A/G | 1.66882e-05 | 0.00288857 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919714 | TTCAACCTTTCCAGG[A/G]CTATTTTGACATAAA | 59349 |
rs746023146 | snp | A/G | 1.64768e-05 | 0.00287021 | synonymous-codon, intron-variant | KLHL12 | GRCh38.p7 | 1:202896935 | GCTTCCAAAGCCCCC[A/G]ACCACCAAAAGCACT | 59349 |
rs746098017 | snp | C/T | 3.29457e-05 | 0.00405854 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202925058 | CTCTACTCTCAATGT[C/T]ACATCACAGAGGGTA | 59349 |
rs746163175 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202898750 | ACAGGATGGAAACTT[C/T]TGGATTAAAACGAGA | 59349 |
rs746176907 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202913598 | AGAAAAATGAACAAT[C/T]TCACTATTATTGCAT | 59349 |
rs746191035 | snp | A/T | 1.68168e-05 | 0.00289967 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924936 | CTAGAGTTCCACGGG[A/T]TTCATTTGTGTGGGG | 59349 |
rs746285996 | snp | A/G | 1.64806e-05 | 0.00287054 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202893350 | ATGTTGTATGCTTCA[A/G]CGGAAGAAAGGTGGG | 59349 |
rs746373912 | snp | G/T | 1.79252e-05 | 0.0029937 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893210 | GCTCTGGCTACATAT[G/T]GAGTCTGGATTCGTT | 59349 |
rs746542042 | in-del | -/AAAC | 1.6679e-05 | 0.00288777 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894761 | ATATCTGCTCAGAAT[-/AAAC]AAATTACAGACTATT | 59349 |
rs746570202 | snp | A/G | 6.53616e-05 | 0.00571634 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925219 | GCAACTACAAGAGGG[A/G]AAAAAAAACAATGAG | 59349 |
rs746633445 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202898475 | TTATTTCAAAAGCCA[A/G]TATATTACTATGAGA | 59349 |
rs746754892 | snp | C/T | 8.87863e-05 | 0.00666223 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894291 | TATCCTCCTGGAAGA[C/T]AGAGACCATTCCAGA | 59349 |
rs746767687 | snp | C/T | 1.67497e-05 | 0.00289389 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918436 | ATAGTTGGACAGGTG[C/T]GATCTAGGATATATT | 59349 |
rs746978187 | snp | C/T | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891791 | ATGCTGTCTCCAGTG[C/T]GAAAGACCTCGGGGA | 59349 |
rs746985573 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202907857 | AGGCTGCAGTGAACC[A/G]AGATCACGCCACTGC | 59349 |
rs747151305 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202909703 | ACTGTGTCAATAGGG[C/T]TTCCTATGCCTTCTA | 59349 |
rs747152767 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202923353 | AAATGCTTCTGATGA[C/T]CTTGGGTATATCTCA | 59349 |
rs747177473 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202902337 | CGGGAGGCTGAGGCA[A/G]GAGAATCGCTTGAAC | 59349 |
rs747234339 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202916581 | CCCAGAAGGTGAAGG[C/T]TACAGTGAGCTGAGA | 59349 |
rs747307536 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202910896 | TTCGCTTTTCTTAGA[A/G]ATATGCTTGGGGACT | 59349 |
rs747396523 | snp | A/G | 1.64776e-05 | 0.00287028 | missense | KLHL12 | GRCh38.p7 | 1:202911130 | AGCAGGTTAGGCAAG[A/G]ATTCTTCCCGCTCTT | 59349 |
rs747477655 | in-del | -/A | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202922435 | AGCCAGGCGTCAAGG[-/A]AAAAAAAAAAAAGAG | 59349 |
rs747481576 | snp | C/G | | | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202925088 | ATTGCTCTTCCTGAG[C/G]GAGTTCATTGAATTG | 59349 |
rs747535018 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927342 | CACGTGACCTGTCTG[C/T]ACCCTAGCGCGGGGC | 59349 |
rs747562954 | snp | A/G | 1.66045e-05 | 0.00288132 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909160 | GAGTTAGGCACTGGG[A/G]ATACCTGTAATACTA | 59349 |
rs747670995 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202894628 | GGCCACTACGAGTCC[A/G]GCACCTTCCCGGGCT | 59349 |
rs747680787 | snp | A/G | 8.86407e-05 | 0.00665676 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202894239 | TCCTGTATGAGGGTC[A/G]TATTTCTCAACTGAA | 59349 |
rs747781506 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202910822 | TGTAAAACAGACAGC[A/C]AAACACAAAATTGAA | 59349 |
rs747781700 | in-del | -/A | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202909233 | AGAAAACCAGTTTGC[-/A]AAAGCCCTGTGATTC | 59349 |
rs747817946 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202895428 | CCTTAATTTTTTCTC[C/T]GTATTTCATGCTCCT | 59349 |
rs747825057 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202896417 | GCTGGTCTTGAACTC[C/T]TGGCCTCAAGAGATC | 59349 |
rs747867521 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202905127 | GCATTTCCCTTCTAG[A/G]ACTTCTGAAAAATAA | 59349 |
rs748080354 | snp | C/T | 3.29451e-05 | 0.00405851 | synonymous-codon, intron-variant | KLHL12 | GRCh38.p7 | 1:202896869 | TGGCAAAAAGCTCCA[C/T]TCCTGAGTCTTGGGG | 59349 |
rs748100635 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202918530 | AGATTAGAAATTCTA[C/T]GCTTAAGGAACTTAA | 59349 |
rs748175504 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202900793 | CGCTTGAACCTGGGA[C/G]ATGCAGGTTGCAGTG | 59349 |
rs748178773 | snp | A/G | 1.64798e-05 | 0.00287047 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202919861 | AATTTCCATGGTAGA[A/G]GCAGTCAAACCTTGG | 59349 |
rs748263548 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202902154 | ACACAAATGGGGGCC[A/G]GGCACAGTGGCTAGC | 59349 |
rs748268515 | snp | G/T | 6.63295e-05 | 0.0057585 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919735 | TTGACATAAACAATA[G/T]CAAGTTTTAATGTCT | 59349 |
rs748307905 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202914012 | TTCTACAGCAAAAAA[G/T]AACTGGCAGCTTGAG | 59349 |
rs748386137 | snp | C/T | 3.29538e-05 | 0.00405904 | synonymous-codon, utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892587 | CTGGGTTCCCATGGA[C/T]GTCACGACTTCCCAG | 59349 |
rs748412044 | snp | A/G | 1.65594e-05 | 0.0028774 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909144 | AATATAGCAGACAGC[A/G]GAGTTAGGCACTGGG | 59349 |
rs748500586 | snp | C/T | 1.65803e-05 | 0.00287922 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892483 | TTTTGATTCTCCCAC[C/T]AACTGTCCACTGGAC | 59349 |
rs748544482 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202924209 | CACTACCTGTATTCT[C/T]TCAAGCCAACCTTTT | 59349 |
rs748613622 | snp | A/G/T | 4.94306e-05 | 0.00497124 | missense | KLHL12 | GRCh38.p7 | 1:202909024 | CCTAGGCGAGCCCTT[A/G/T]TCCTGGGTCCCTGCA | 59349 |
rs748739319 | in-del | -/AT | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202919653 | CAAACATGAACATCC[-/AT]AGTTTGTCTCCAAAA | 59349 |
rs748779851 | in-del | -/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202916874 | AGCTACACAGGAGGA[-/T]GAGGTGGGAGAGCTG | 59349 |
rs748796274 | snp | C/T | | | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929711 | GTTCAGAGCCTGGTG[C/T]GGTGGTGTACACCTA | 59349 |
rs748842460 | in-del | -/A | | | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927674 | AGAATGAGACCCTGT[-/A]AAAAAAAAAAAAAAA | 59349 |
rs748878281 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202923049 | TATACAGAATTGCTA[A/C]GAGAACTAAGCCTAG | 59349 |
rs749024855 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202917118 | CTCTGCTACTGGTAC[G/T]CTGATTTAGAATTAG | 59349 |
rs749111676 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202903772 | GGATTACAGGCATGC[A/G]TCACCATGCCTGGCT | 59349 |
rs749228480 | snp | C/T | 1.65999e-05 | 0.00288091 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202895537 | CTCCCAGGGTGGTGG[C/T]TCCAGCAAGACCTCG | 59349 |
rs749295165 | snp | A/G | 3.29544e-05 | 0.00405908 | missense, utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892571 | CACCAGCATCACAGC[A/G]CTGGGTTCCCATGGA | 59349 |
rs749408890 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202913743 | TGAGTAGCAGTTAGC[C/T]AGGGGGAGTAAGAGA | 59349 |
rs749527658 | snp | A/G | 6.59446e-05 | 0.00574177 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908995 | TCCCCTCATTCTGCC[A/G]AGATACCAGCTTACC | 59349 |
rs749595877 | in-del | -/A | 3.67627e-05 | 0.00428719 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894330 | TAAATCCTCATGCCC[-/A]TTCCTGGTCGGTTTT | 59349 |
rs749703275 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202921302 | GCCTCAGCCGCCTGA[A/G]TAGCTGGGACTACAG | 59349 |
rs749714699 | snp | G/T | 1.64732e-05 | 0.0028699 | missense | KLHL12 | GRCh38.p7 | 1:202925078 | CACAGAGGGTATTGC[G/T]CTTCCTGAGGGAGTT | 59349 |
rs749733481 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202900602 | GGCGTGGTGGCTCAC[A/G]CCTGTAATCACAGCA | 59349 |
rs749832286 | snp | A/G | 9.08967e-05 | 0.00674093 | missense | KLHL12 | GRCh38.p7 | 1:202894207 | TTGGTGGCCATTGGT[A/G]TAACATTAGTCCAAT | 59349 |
rs749871310 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202908305 | CTTGCCCAACCAGTC[A/G]TTGCTGGGGCTTGGA | 59349 |
rs749876703 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202901787 | TTTTGATAACTATGA[C/G]AGCAACAGTGTTTCA | 59349 |
rs749976867 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202922826 | TTAGCTAGTAAGAGA[C/G]AGATATCATTCTTAT | 59349 |
rs750058530 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202915991 | TATATGTAGTGAACG[C/T]CAAATCTGTAGTGCT | 59349 |
rs750065681 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202910685 | TTCATGCTGGCTTTA[A/C]CAGAAGTCAAAAATG | 59349 |
rs750075682 | snp | A/C | 1.64876e-05 | 0.00287116 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202895654 | GGCCATCATAGCCAC[A/C]AATGACGTAGATCCG | 59349 |
rs750122033 | snp | C/T | 8.24029e-05 | 0.00641831 | missense | KLHL12 | GRCh38.p7 | 1:202924999 | GCACAGAAGTAATCA[C/T]TACAGGCAGCCAGCA | 59349 |
rs750254391 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202896151 | TCAGAAATTACTATT[A/G]TTCATTCAGCACTGA | 59349 |
rs750328114 | snp | A/G | 1.67595e-05 | 0.00289473 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202893264 | CATAGAGTCTCCCCC[A/G]AAGCACTGTGGCCCC | 59349 |
rs750359660 | in-del | -/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202899651 | TCTAACATGGCAAAA[-/C]CCCGTCTCTACTAAA | 59349 |
rs750362890 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202909153 | GACAGCAGAGTTAGG[C/T]ACTGGGGATACCTGT | 59349 |
rs750368622 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202924011 | TTGAAAAAATAAATC[A/G]AGATAATTTATTTAA | 59349 |
rs750397673 | snp | A/T | 1.66557e-05 | 0.00288575 | intron-variant | KLHL12 | GRCh38.p7 | 1:202892684 | AAAGAAGCAAAAGAA[A/T]GAAATGAGTCAGCTG | 59349 |
rs750485982 | snp | C/G | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891409 | AAAATCTACACTAAA[C/G]GACAGGTAAGGAAAA | 59349 |
rs750512668 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202907026 | TATACAAATATTTTC[C/T]TATAATTTCTTCTAA | 59349 |
rs750638252 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202917509 | GCCACTGCACCTGGC[C/T]TACTATTCCTTTAAC | 59349 |
rs750663868 | snp | C/T | 3.29636e-05 | 0.00405964 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894572 | GTTCCCTCCCATTCC[C/T]GCATCCCAGACTCAA | 59349 |
rs750693407 | snp | C/G | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891480 | TACAAACCACTCCTT[C/G]GCAGACATGTGCTTC | 59349 |
rs750753403 | snp | C/G | 9.65391e-05 | 0.00694696 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894144 | TATGTAAAGGTCTGA[C/G]AGCATCGCCTATTGT | 59349 |
rs750771168 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202914733 | TAGCCAGGTGTGGTG[C/T]GCACGCCTGTGGTCC | 59349 |
rs750847706 | snp | A/G | 1.64738e-05 | 0.00286995 | stop-gained | KLHL12 | GRCh38.p7 | 1:202918263 | CAGGAAAATGCTTCT[A/G]GCTAAAAACCTCAGC | 59349 |
rs750948732 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926696 | CAAGTCTCAGCATAT[C/T]CTTCATCCTCACCCT | 59349 |
rs751081191 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202901121 | AAGGGTGGGAGAAAA[C/G]AAGTAGAAAGGAAAT | 59349 |
rs751086647 | snp | C/T | 1.64792e-05 | 0.00287042 | synonymous-codon, intron-variant | KLHL12 | GRCh38.p7 | 1:202895616 | TGTGTAGTCTAGACA[C/T]TCCACTGAACTAAGG | 59349 |
rs751141092 | snp | A/C | 1.66125e-05 | 0.00288201 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919920 | AGAGCTGAAAATTCA[A/C]AAGGTATAAAAGAAT | 59349 |
rs751151515 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202905866 | CTGGAGTGCAGTGGC[A/G]TGATCTCAGCTTACT | 59349 |
rs751176821 | snp | C/T | 1.7336e-05 | 0.00294409 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895472 | AGAGGTTAAAAACCC[C/T]GGTCCAGCCACAGTA | 59349 |
rs751279335 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202914447 | CTTAAAACTTTTATA[C/T]GATTGGAAAATAGTT | 59349 |
rs751279414 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202900221 | TATAACTCCCTGCCC[C/T]ACCCCCCAACCCCCC | 59349 |
rs751306766 | snp | C/T | 1.65042e-05 | 0.0028726 | missense, synonymous-codon | KLHL12 | GRCh38.p7 | 1:202892649 | TACTTAGCAGGGAAT[C/T]ACCATCATATCTGAG | 59349 |
rs751453489 | snp | A/G | 4.94735e-05 | 0.00497336 | synonymous-codon, utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892542 | CAATGGTCACTTCTC[A/G]CGGAGAACACAAACA | 59349 |
rs751476466 | in-del | -/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202921618 | ATTGTTAGCAGTATA[-/T]TTAGTCTAAATTGTT | 59349 |
rs751488344 | in-del | -/A | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202912673 | CCAAACCACGAAACC[-/A]AGGTGGCTATGGTGG | 59349 |
rs751490390 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202919659 | TGAACATCCATAGTT[G/T]GTCTCCAAAATGTTC | 59349 |
rs751525786 | snp | C/T | | | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202918228 | ACTCAGAAGAATGAA[C/T]TCTTCATGCTGTACC | 59349 |
rs751549631 | snp | A/T | 1.64754e-05 | 0.00287009 | missense | KLHL12 | GRCh38.p7 | 1:202909081 | TGAAACTTCTTTGCT[A/T]CATCAACCAGATCCC | 59349 |
rs751612295 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904731 | GGGAAGGGGAGTGTG[C/T]GTGTGCTGTGACACG | 59349 |
rs751660242 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202919134 | GGTGGCATGCACCTG[A/T]GGTCCCAGCTACTCA | 59349 |
rs751671183 | snp | C/T | 3.49125e-05 | 0.00417792 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893461 | AGCAAATGTATGGTA[C/T]TAAGCCTAGAATCTG | 59349 |
rs751780981 | in-del | -/A | 1.6599e-05 | 0.00288084 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919919 | GAGAGCTGAAAATTC[-/A]AAAGGTATAAAAGAA | 59349 |
rs751815195 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202918246 | TTCATGCTGTACCAC[C/T]TCAGGAAAATGCTTC | 59349 |
rs751842625 | snp | C/T | 1.64798e-05 | 0.00287047 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202893338 | GAATCAGTGCGAATG[C/T]TGTATGCTTCAACGG | 59349 |
rs751878042 | snp | A/G | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892263 | AAATGACAGGAAAGT[A/G]CTCCCCAAAGCAGTG | 59349 |
rs751895202 | snp | C/T | 4.98965e-05 | 0.00499457 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911247 | TCCTACTTTTCCAAT[C/T]AGCTCACCATCTCAA | 59349 |
rs751898555 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926607 | CCGGGGGGTCTTTTA[C/T]CGTTTCCGTGTCAAA | 59349 |
rs752216707 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202913157 | AGATATATTTAATTA[A/T]TCATCTGGGGAACTT | 59349 |
rs752229257 | snp | C/T | 1.64803e-05 | 0.00287052 | missense | KLHL12 | GRCh38.p7 | 1:202919790 | GCTGCAGGAAGCAGT[C/T]CTTGTACATTCTCCA | 59349 |
rs752324875 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202925436 | CGGAGTGTCCCTACC[A/G]CTTGACATTTAATAT | 59349 |
rs752332039 | in-del | -/AA | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202899832 | CATCTCAAAAAAAAA[-/AA]AAAAAAATAATAATA | 59349 |
rs752399607 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202909062 | CCGAAGTTCAGGCCT[C/T]AGATGAAACTTCTTT | 59349 |
rs752416960 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926550 | GCAACTCTAGGGGTG[C/T]AAAAAGGTCTAGAAC | 59349 |
rs752416977 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911970 | AGACCCAAACACCAA[A/G]TGCTCCAGGGGCTTT | 59349 |
rs752509085 | in-del | -/GTAA | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202918093 | TATGAAGCCCTGATG[-/GTAA]GTAACTGCATCCTAT | 59349 |
rs752543644 | snp | A/C | 1.65157e-05 | 0.0028736 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908964 | GTTGTCACCTGCAAG[A/C]AGTAGTTGAAAAGCA | 59349 |
rs752563420 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202920844 | ATTAAAATACAGATG[A/T]ATTTACAGAATAGAA | 59349 |
rs752680158 | snp | A/C | 1.64817e-05 | 0.00287064 | stop-gained | KLHL12 | GRCh38.p7 | 1:202925159 | GGGCCATAATGCCTC[A/C]CATAAAGCAGTGCGG | 59349 |
rs752706995 | in-del | -/A | 0.00147468 | 0.0271139 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925219 | GCAACTACAAGAGGG[-/A]AAAAAAAACAATGAG | 59349 |
rs752742787 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202916445 | ATGTCAGGAGTTCCA[C/G]AGCAGCCTGGCCACA | 59349 |
rs752775817 | snp | C/T | 1.65941e-05 | 0.00288041 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911226 | TGTATAATTACACAC[C/T]GTGGATCCTACTTTT | 59349 |
rs752883632 | snp | C/T | 1.70679e-05 | 0.00292124 | intron-variant | KLHL12 | GRCh38.p7 | 1:202892710 | AGCTGCGTGCAGTGG[C/T]ACGTGCCTGTAATCC | 59349 |
rs752905625 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202899124 | TTGAGACCAGCCTAG[A/C]CAACAAGGCAAAACC | 59349 |
rs752920483 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202895899 | ACTGAACGAAATGCC[C/T]GTTGTGGTGCTCTTA | 59349 |
rs752925123 | snp | G/T | | | missense | KLHL12 | GRCh38.p7 | 1:202894208 | TGGTGGCCATTGGTG[G/T]AACATTAGTCCAATG | 59349 |
rs753043000 | in-del | -/TC | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911456 | ATATATATATATGTA[-/TC]TCTCTCTCTCTCTCT | 59349 |
rs753124636 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202905531 | ATGTCTTATCTCCTA[A/G]TGCCAGGTTCTTTCC | 59349 |
rs753172357 | snp | C/T | 3.3465e-05 | 0.0040904 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894768 | CTCAGAATAAACAAA[C/T]TACAGACTATTAGAG | 59349 |
rs753219420 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202917966 | GTGATTCTTACCCAC[C/T]GGGATCATATATCTA | 59349 |
rs753226802 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202903078 | AGGTGGGAGGATTGC[C/T]TGAGCCCAGAAAGTG | 59349 |
rs753233771 | in-del | -/GTGGCAC | 3.38424e-05 | 0.0041134 | intron-variant | KLHL12 | GRCh38.p7 | 1:202892706 | AGTCAGCTGCGTGCA[-/GTGGCAC]GTGCCTGTAATCCCA | 59349 |
rs753313109 | snp | C/T | 3.30147e-05 | 0.00406279 | synonymous-codon, utr-variant-5-prime | KLHL12 | GRCh38.p7 | 1:202925172 | TCCCATAAAGCAGTG[C/T]GGAGAAAGAACAAAA | 59349 |
rs753314178 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904301 | AAGGCACCCTGCCAG[A/G]CCAACCCTTTAACCC | 59349 |
rs753407736 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202910748 | TTGGAACAATTTATG[C/T]TTAATGGAGAAGGGG | 59349 |
rs753493316 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904088 | CAATGGCACGATCTT[A/G]GTTCACCACAATCTC | 59349 |
rs753607460 | snp | C/G | 1.64743e-05 | 0.00287 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896843 | CAACGAATGGTTTCA[C/G]CATTATTTACTGGCA | 59349 |
rs753607650 | snp | A/G | 1.64751e-05 | 0.00287007 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202925136 | AGTATTTGTCATTAT[A/G]TCTTTGGGGGCCATA | 59349 |
rs753632801 | in-del | -/CTG | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892335 | TTTTTCCTGGAATAT[-/CTG]CTGTTACCCACCCTT | 59349 |
rs753698311 | snp | G/T | 1.64757e-05 | 0.00287012 | missense | KLHL12 | GRCh38.p7 | 1:202925018 | AGGCAGCCAGCACAA[G/T]CCGATGGGCAGGGAA | 59349 |
rs753812432 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202902378 | GAGACTGCAGTGAGC[C/T]GAGATCACACCATTG | 59349 |
rs753921250 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202893913 | ACTTTATTTAACAGA[C/T]ATTTATTAAGCATGT | 59349 |
rs753939127 | snp | G/T | 9.90606e-05 | 0.00703708 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911040 | TTGGATCCTGAGAGT[G/T]TTGCACTACTTACCT | 59349 |
rs754003681 | snp | A/T | | | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928978 | TGGGAGTACAGGTGC[A/T]CACCACCACGCCCGA | 59349 |
rs754030830 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202907479 | TGGTGGCAGTCGCCT[A/G]TTGTCCCAGCTACTC | 59349 |
rs754074018 | snp | G/T | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891650 | GCAAACATTGCCATG[G/T]CTAGATGAGCCCTGG | 59349 |
rs754095943 | in-del | -/AAG | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202894065 | AGAGAAAACAGAGAC[-/AAG]GAGGAGAGCAGAATC | 59349 |
rs754118094 | snp | C/T | 0.000118043 | 0.00768163 | missense, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928510 | GGAACTTTTTGACAT[C/T]GAGAAAACCCACAGA | 59349 |
rs754213512 | snp | A/G | 1.64749e-05 | 0.00287005 | missense | KLHL12 | GRCh38.p7 | 1:202894602 | ATACCTAGACAGTAG[A/G]TCACTCCACTGGCCA | 59349 |
rs754274931 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202908909 | GAAAAGGTCTGAAAC[A/G]AGGTGTCTGTACTTC | 59349 |
rs754305311 | snp | C/G | 0.000314801 | 0.012542 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918408 | GACAGACACAGGCAG[C/G]AAACACTTTAGAATA | 59349 |
rs754379195 | snp | A/G | 1.73718e-05 | 0.00294714 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202894212 | GGCCATTGGTGTAAC[A/G]TTAGTCCAATGTCCT | 59349 |
rs754396941 | in-del | -/TCTCTC | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911457 | ATATATATATATGTA[-/TCTCTC]TCTCTCTCTCTCTCT | 59349 |
rs754469300 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202918282 | AAAAACCTCAGCTGC[C/T]TGCATCAGGTCAACA | 59349 |
rs754499732 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202896367 | ATTTTTTTGTTTACT[G/T]TTTTGTAGAGACAGA | 59349 |
rs754598827 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202924773 | TAACCATGTGTTACA[C/T]ATTACTATTATCCCT | 59349 |
rs754637326 | in-del | -/AAAAAAAA | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202899826 | AGACTCCATCTCAAA[-/AAAAAAAA]AAAAAAATAATAATA | 59349 |
rs754640403 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202924146 | TACTATACATTTCAA[A/G]TATTTTGTCAGGCAA | 59349 |
rs754734043 | snp | A/C | 1.65825e-05 | 0.00287941 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918412 | GACACAGGCAGCAAA[A/C]ACTTTAGAATAGTTG | 59349 |
rs754787664 | snp | A/C | 1.64727e-05 | 0.00286986 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202896859 | CATTATTTACTGGCA[A/C]AAAGCTCCACTCCTG | 59349 |
rs754822367 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202919295 | ATTGTAAGGGAAAAC[A/C]AACCACCTGTAATCC | 59349 |
rs754878334 | in-del | -/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202899841 | AAAAAAAAAAAAAAA[-/T]AATAATAATAAATAA | 59349 |
rs754879170 | snp | A/G | 1.64735e-05 | 0.00286993 | missense | KLHL12 | GRCh38.p7 | 1:202925030 | CAATCCGATGGGCAG[A/G]GAAGTCTTTCTGCTC | 59349 |
rs754879214 | snp | A/G | 1.65255e-05 | 0.00287445 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202895680 | ATCCGGTCATGAAGG[A/G]ACACTGAGGCCACAT | 59349 |
rs754941428 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202897680 | ACTCTCCTAACCTTG[C/T]CACAAAAAAAGCTAC | 59349 |
rs754994863 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202893965 | TAGATATTCTAAAAC[A/G]TAGGGAGAGAACAAA | 59349 |
rs755045797 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202919552 | CTCTCTTTTATAGAG[A/C]CAAATACTCATATCT | 59349 |
rs755057512 | snp | C/T | | | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928987 | AGGTGCACACCACCA[C/T]GCCCGACTAATTTTT | 59349 |
rs755095286 | snp | C/T | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891726 | CCCAGTTATACTGAA[C/T]TCCCACATTGATGTC | 59349 |
rs755130710 | snp | C/T | 4.95282e-05 | 0.00497611 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911041 | TGGATCCTGAGAGTG[C/T]TGCACTACTTACCTC | 59349 |
rs755150140 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202894070 | AAACAGAGACAAGGA[A/G]GAGAGCAGAATCTCA | 59349 |
rs755157303 | snp | C/T | 1.6477e-05 | 0.00287024 | synonymous-codon, utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892572 | ACCAGCATCACAGCG[C/T]TGGGTTCCCATGGAT | 59349 |
rs755169723 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202914967 | TTGTAAACACCACTG[C/T]CCTCAGACTAGCCAT | 59349 |
rs755186933 | snp | A/G | | | synonymous-codon, utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892545 | TGGTCACTTCTCGCG[A/G]AGAACACAAACACCA | 59349 |
rs755201509 | in-del | -/TTCTT | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202893651 | ATAAAAATGGTTCTC[-/TTCTT]TACTTTCATTAACTC | 59349 |
rs755240900 | snp | G/T | 0.00011828 | 0.00768935 | missense, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928537 | CAGAGGCCTCAAATT[G/T]ATTCACGTCCATTGT | 59349 |
rs755247295 | snp | A/C | 1.65053e-05 | 0.0028727 | missense | KLHL12 | GRCh38.p7 | 1:202909121 | AACTACAGCGGATGA[A/C]AGGCTGAAATATAGC | 59349 |
rs755401202 | snp | A/C | 1.6863e-05 | 0.00290365 | missense, utr-variant-5-prime | KLHL12 | GRCh38.p7 | 1:202925199 | AAAATGGGTCCTTGG[A/C]TTCTGCAACTACAAG | 59349 |
rs755504307 | snp | C/T | 1.64735e-05 | 0.00286993 | missense | KLHL12 | GRCh38.p7 | 1:202894621 | CTCCACTGGCCACTA[C/T]GAGTCCGGCACCTTC | 59349 |
rs755550707 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202916327 | AGTCACTAGAGAAAG[A/G]TGTAAAGAAACACTT | 59349 |
rs755566576 | snp | C/G | 3.32557e-05 | 0.00407759 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918165 | AACATCAAGACAAAT[C/G]CGTACCTGAATTTCG | 59349 |
rs755713061 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202902878 | CACCTGTAGTCCCAA[C/G]TCCCAGCTACCTGGG | 59349 |
rs755742112 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202909214 | AATAATTAACTTCTG[A/G]CTACAGAAAACCAGT | 59349 |
rs755872768 | snp | A/C/T | 3.29811e-05 | 0.00406075 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202895660 | CATAGCCACCAATGA[A/C/T]GTAGATCCGGTCATG | 59349 |
rs755922107 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202896173 | CAGCACTGAGAGACA[C/T]GCTGAGGGAGACAGA | 59349 |
rs755925130 | snp | C/T | 8.33674e-05 | 0.00645575 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919941 | ATAAAAGAATGATGG[C/T]TATAATTCCACAAGA | 59349 |
rs756016242 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202924078 | CAAAGATTTGCAATG[C/T]TATTTTCTGTTCAGC | 59349 |
rs756018685 | snp | A/C/T | 3.29578e-05 | 0.00405931 | missense | KLHL12 | GRCh38.p7 | 1:202919854 | CCAATAAAATTTCCA[A/C/T]GGTAGAGGCAGTCAA | 59349 |
rs756141639 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202907095 | TCTTGTGTTGATATG[C/T]ATCTGTGTATAAAGC | 59349 |
rs756175045 | snp | A/G | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891505 | TGCTTCTAAAAGAAT[A/G]GGGCAGTAATCAGGT | 59349 |
rs756289171 | snp | C/T | 0.000118772 | 0.00770531 | missense, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928482 | CAAGTATGTTTTACC[C/T]TCCAGGTACTGAGGA | 59349 |
rs756328245 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926844 | GAAACGAAGTCCTTC[C/T]TCCTAATACCACCAG | 59349 |
rs756361481 | in-del | -/AT | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891487 | CACTCCTTGGCAGAC[-/AT]GTGCTTCTAAAAGAA | 59349 |
rs756517742 | snp | C/T | 0.000186619 | 0.00965789 | missense | KLHL12 | GRCh38.p7 | 1:202894189 | CTGGTCTTACCAGAA[C/T]GCTTGGTGGCCATTG | 59349 |
rs756536034 | in-del | -/G | 0.000193592 | 0.00983659 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894136 | CATTATATATGTAAA[-/G]GGTCTGACAGCATCG | 59349 |
rs756547151 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202901694 | CTTCATTATTTTTCC[C/T]GACAGATCCTGTGTT | 59349 |
rs756588739 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202913651 | GCTATGAGACAGAAC[A/C]ACATGAGATTTCCTA | 59349 |
rs756627787 | in-del | -/A | 0.00147468 | 0.0271139 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925218 | GCAACTACAAGAGGG[-/A]AAAAAAAAACAATGA | 59349 |
rs756641797 | snp | A/T | 1.64738e-05 | 0.00286995 | missense | KLHL12 | GRCh38.p7 | 1:202918271 | TGCTTCTGGCTAAAA[A/T]CCTCAGCTGCTTGCA | 59349 |
rs756700248 | snp | G/T | | | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928959 | CTCAGCCTCTCCGAG[G/T]AGCTGGGAGTACAGG | 59349 |
rs756860054 | snp | A/C | 1.66161e-05 | 0.00288232 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919922 | AGCTGAAAATTCAAA[A/C]GGTATAAAAGAATGA | 59349 |
rs756879807 | snp | A/G | 1.64846e-05 | 0.0028709 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202895639 | AACTAAGGCGGGAAC[A/G]GCCATCATAGCCACC | 59349 |
rs756887882 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202920998 | TAGTTCCTATCATCT[C/G]TCCTTAGACTACTTT | 59349 |
rs756969803 | snp | A/C | 1.72716e-05 | 0.00293862 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895484 | CCCTGGTCCAGCCAC[A/C]GTAAGATGGAAATAA | 59349 |
rs757022484 | snp | C/T | 1.64784e-05 | 0.00287035 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202919831 | TACTGTTTCTGTGTA[C/T]ACAAAGTCCAATAAA | 59349 |
rs757050363 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202894339 | ATGCCCATTCCTGGT[C/T]GGTTTTTTTCTGAGT | 59349 |
rs757070593 | snp | A/C | | | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929326 | AAAATTTTCCTTCAC[A/C]TATACTCGTGCACAT | 59349 |
rs757077478 | snp | C/T | 3.30524e-05 | 0.00406511 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909133 | TGAAAGGCTGAAATA[C/T]AGCAGACAGCAGAGT | 59349 |
rs757132164 | snp | C/T | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891979 | AGATGAGTCTCTCTC[C/T]CCCTTGTCCCCAAAG | 59349 |
rs757223517 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202907869 | ACCGAGATCACGCCA[C/T]TGCACTCCACCCTGG | 59349 |
rs757223907 | snp | A/C | 0.000164821 | 0.00907652 | missense | KLHL12 | GRCh38.p7 | 1:202925160 | GGCCATAATGCCTCC[A/C]ATAAAGCAGTGCGGA | 59349 |
rs757301002 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, intron-variant | KLHL12 | GRCh38.p7 | 1:202896884 | CTCCTGAGTCTTGGG[A/G]TCATATTTCTCTACC | 59349 |
rs757317497 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904846 | CAAAAAAGGAGACAG[C/T]CACAAATTAGAAAAG | 59349 |
rs757363997 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202914201 | AGTGATATGATCATA[C/T]TGATGTTTTGTAAAG | 59349 |
rs757384843 | snp | C/T | 6.58903e-05 | 0.00573941 | missense | KLHL12 | GRCh38.p7 | 1:202925041 | GCAGGGAAGTCTTTC[C/T]GCTCTACTCTCAATG | 59349 |
rs757483499 | snp | C/G | | | missense | KLHL12 | GRCh38.p7 | 1:202918250 | TGCTGTACCACTTCA[C/G]GAAAATGCTTCTGGC | 59349 |
rs757484908 | snp | A/C | 1.74964e-05 | 0.00295769 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893464 | AAATGTATGGTACTA[A/C]GCCTAGAATCTGAAT | 59349 |
rs757492661 | snp | C/T | 1.648e-05 | 0.0028705 | synonymous-codon, intron-variant | KLHL12 | GRCh38.p7 | 1:202893343 | AGTGCGAATGTTGTA[C/T]GCTTCAACGGAAGAA | 59349 |
rs757529857 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202912282 | ACCTTTGATGACCAT[C/G]ACTCTGTGAATAAGA | 59349 |
rs757608012 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926675 | GGGATTCCTGCCTCA[A/T]CACTCCAAGTCTCAG | 59349 |
rs757637307 | snp | G/T | 1.66405e-05 | 0.00288443 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911249 | CTACTTTTCCAATTA[G/T]CTCACCATCTCAAAA | 59349 |
rs757703466 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B | KLHL12, RABIF | GRCh38.p7 | 1:202891096 | CTACTAAAGGCAATG[C/T]TGGTTAGCCACAAAC | 59349 |
rs757726980 | snp | G/T | 1.64781e-05 | 0.00287033 | missense | KLHL12 | GRCh38.p7 | 1:202911133 | AGGTTAGGCAAGGAT[G/T]CTTCCCGCTCTTTCT | 59349 |
rs757911716 | snp | C/T | 5.01953e-05 | 0.00500951 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894769 | TCAGAATAAACAAAT[C/T]ACAGACTATTAGAGA | 59349 |
rs757999772 | snp | C/T | 1.64789e-05 | 0.0028704 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202919807 | TTGTACATTCTCCAC[C/T]GTCACATGTACTGTT | 59349 |
rs758020285 | in-del | -/TAGG | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926542 | ACTTAGTTGCAACTC[-/TAGG]GGTGTAAAAAGGTCT | 59349 |
rs758052074 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202912133 | TTAACTGTGAAAAAG[A/G]TATTTGTTGGCAGCA | 59349 |
rs758092268 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202920957 | AGGAGCCTGTGGGTT[A/G]TAACTCCAGTCTCTC | 59349 |
rs758259893 | snp | A/G | 4.95511e-05 | 0.00497726 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908968 | TCACCTGCAAGAAGT[A/G]GTTGAAAAGCATCCC | 59349 |
rs758465114 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202916478 | AGTGAAACTCCGTCT[C/T]TGCTAAAAATACAAA | 59349 |
rs758557076 | snp | C/G | 1.64795e-05 | 0.00287045 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202893329 | GTTGTCCAGGAATCA[C/G]TGCGAATGTTGTATG | 59349 |
rs758600116 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202903311 | TCTCTGACACTCTGG[A/T]AGGCAAAAAATTATG | 59349 |
rs758641282 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202896116 | CTTAAAAGGTAGGAG[G/T]GTTGGATTTCCATGT | 59349 |
rs758691818 | snp | C/T | 1.79703e-05 | 0.00299747 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893194 | GATCACATAGACTCT[C/T]GCTCTGGCTACATAT | 59349 |
rs758732222 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202924295 | TCAACGCCTGTACAG[C/T]TATTCATTAAAAACT | 59349 |
rs758813870 | in-del | -/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202893628 | CTTGAAATGATAAAA[-/G]ATAAATAATAAAAAT | 59349 |
rs758824454 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202925510 | GTAAATCTTGACAAG[A/G]TTCTTGTCTCAAATG | 59349 |
rs758828609 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911473 | CTCTCTCTCTCTCTC[G/T]CTCTCTAAGATAGAT | 59349 |
rs758876070 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202914002 | AACAGCTCTGTTCTA[C/T]AGCAAAAAAGAACTG | 59349 |
rs758970747 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904302 | AGGCACCCTGCCAGG[A/C]CAACCCTTTAACCCT | 59349 |
rs759002174 | snp | A/G | 3.29554e-05 | 0.00405914 | synonymous-codon, utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892608 | GACTTCCCAGCTGTC[A/G]ATGATAGGGTCATAA | 59349 |
rs759018927 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | KLHL12, RABIF | GRCh38.p7 | 1:202890892 | CAAGTAACTCCAAGC[A/G]TCAGAGGGGCTAATG | 59349 |
rs759025544 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202915324 | CTTCCCATTGTTTTA[A/G]GTACTATTATTTTAT | 59349 |
rs759096127 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926438 | TCTATAAGCACTATA[A/G]ATAATTCCTCCAACA | 59349 |
rs759208003 | in-del | -/CTTCTGACTTT | | | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202930389 | AGGAACTAGTTCAGA[-/CTTCTGACTTT]CTTCTGACTTTTTTC | 59349 |
rs759250314 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202905322 | CATTAGCTTTTAGTT[C/G]AATTTAATAAGCAAA | 59349 |
rs759257866 | snp | C/T | 3.30617e-05 | 0.00406568 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897012 | GCATCCCTGGATGGG[C/T]AACTAGTCACAGGGA | 59349 |
rs759347713 | snp | C/T | 1.64751e-05 | 0.00287007 | missense | KLHL12 | GRCh38.p7 | 1:202925141 | TTGTCATTATGTCTT[C/T]GGGGGCCATAATGCC | 59349 |
rs759407862 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202900939 | TAGTCCCAGCTACTC[C/T]GGAGGCTGAGGCAGG | 59349 |
rs759503243 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202905115 | GAAACTGCTTCAGCA[C/T]TTCCCTTCTAGAACT | 59349 |
rs759526552 | snp | A/C | 3.67762e-05 | 0.00428798 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894320 | GAAAGAGTGGTAAAT[A/C]CTCATGCCCATTCCT | 59349 |
rs759558651 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202906701 | GAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTAC | 59349 |
rs759590208 | in-del | -/AGGT | 1.66101e-05 | 0.0028818 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919922 | AGCTGAAAATTCAAA[-/AGGT]ATAAAAGAATGATGG | 59349 |
rs759622136 | snp | A/T | 1.65567e-05 | 0.00287716 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911207 | TTCAGAATCCACCTG[A/T]AAATGTATAATTACA | 59349 |
rs759643929 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202895846 | TCATGAACCCTCCTT[A/C]AGTGGTTCATCCTCA | 59349 |
rs759713417 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202923249 | TGACAAAAAACAGGA[C/T]GCACAACATATAATT | 59349 |
rs759799894 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202908812 | ATTTCCAAATAATTA[C/T]GTGAAGTAGATAGAG | 59349 |
rs759902237 | snp | A/T | 1.64841e-05 | 0.00287085 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202895579 | TAGGGGCCACAGAAT[A/T]CCAGACCCCATCCTC | 59349 |
rs759956130 | snp | C/G | 1.64906e-05 | 0.00287142 | missense | KLHL12 | GRCh38.p7 | 1:202919762 | GTCTGTACCTTTCAA[C/G]TGAAGCAGACAGGCT | 59349 |
rs759990156 | snp | C/T | 3.3012e-05 | 0.00406262 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202919894 | GTCAACATAAGGTTT[C/T]CCCTTCTCTGAGAGC | 59349 |
rs760062306 | snp | G/T | 3.29484e-05 | 0.00405871 | missense | KLHL12 | GRCh38.p7 | 1:202909042 | CTGGGTCCCTGCATC[G/T]GACTCCGAAGTTCAG | 59349 |
rs760136279 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202905198 | CTTAAGGTCAGGGCA[A/G]TAAGCAAGTTCTCTA | 59349 |
rs760178156 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904080 | CTGGAGTGCAATGGC[A/G]CGATCTTGGTTCACC | 59349 |
rs760272199 | in-del | -/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202897971 | CAACAAAAGACTAGA[-/G]TTTTAAAGGAAAAGT | 59349 |
rs760281955 | snp | A/C | 3.30311e-05 | 0.0040638 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897001 | GGGTTAGTTCAGCAT[A/C]CCTGGATGGGTAACT | 59349 |
rs760314501 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | KLHL12 | GRCh38.p7 | 1:202925130 | AGCATGAGTATTTGT[C/T]ATTATGTCTTTGGGG | 59349 |
rs760396388 | snp | A/G | 1.64781e-05 | 0.00287033 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202925004 | GAAGTAATCACTACA[A/G]GCAGCCAGCACAATC | 59349 |
rs760403190 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202917674 | TTCTTCTTTCTTCTA[C/T]GTAATGTCCTTACTT | 59349 |
rs760472119 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926273 | TTACTGTTAAAGAAT[A/C]GATATTGGAATCCAA | 59349 |
rs760589125 | snp | A/G | 1.7013e-05 | 0.00291654 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893429 | CTACTCCTGCACCTG[A/G]GGAAAATGAATGCAT | 59349 |
rs760658101 | in-del | -/A | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202922800 | GAAGATCCAAGACTT[-/A]AACCAGTCACTTAGC | 59349 |
rs760675167 | snp | A/G | 1.64784e-05 | 0.00287035 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202918189 | AATTTCGTCGCACTT[A/G]ATTAGCTTTTCCACC | 59349 |
rs760677247 | snp | C/T | 3.30327e-05 | 0.0040639 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202893290 | GCCCCTACATAGCAT[C/T]GTGGAGTGGTCATAC | 59349 |
rs760784295 | snp | C/T | 1.64928e-05 | 0.00287161 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202895564 | CTCGTCGGACATTCA[C/T]AGGGGCCACAGAATA | 59349 |
rs760835503 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202919405 | CAGATAGATAAAGAG[C/T]ATCCATGTAGGCTAT | 59349 |
rs760900918 | snp | C/T | 1.6588e-05 | 0.00287988 | missense | KLHL12 | GRCh38.p7 | 1:202894740 | AAGCCTCCAGAGACA[C/T]AGATCATATCTGCTC | 59349 |
rs760985752 | in-del | -/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911421 | GGGTTAAAAAAAAAA[-/T]ATATATATATACACA | 59349 |
rs760991951 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202916011 | TCTGTAGTGCTCATT[C/G]TATTCATTGTATTTT | 59349 |
rs760996202 | snp | C/T | 1.65455e-05 | 0.00287619 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918401 | CACCTAGGACAGACA[C/T]AGGCAGCAAACACTT | 59349 |
rs761002302 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202893845 | AGCCTGCTCCACTTC[A/G]AAAAGCTCTTGGTGA | 59349 |
rs761061209 | snp | C/T | 1.65269e-05 | 0.00287457 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919746 | AATAGCAAGTTTTAA[C/T]GTCTGTACCTTTCAA | 59349 |
rs761100558 | snp | C/G | 1.65707e-05 | 0.00287838 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892495 | CACTAACTGTCCACT[C/G]GACTGGTCACTAGCT | 59349 |
rs761160553 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202893732 | GGTGGCAATAAAGGT[A/G]GATGGAGGGAAAGGA | 59349 |
rs761210087 | in-del | -/AA | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202898222 | CTTTTTTCAAAGAGC[-/AA]AGTCTCTTTGAGAAA | 59349 |
rs761292901 | snp | C/T | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891369 | GGATTTTGGTTGTCC[C/T]TGATTATTCTGTCCT | 59349 |
rs761350454 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202902603 | AAACAATCACATAAA[C/T]AACCCTGTGATAAAT | 59349 |
rs761368712 | snp | A/G | 1.64817e-05 | 0.00287064 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896809 | GGAGGCAGAGACTGA[A/G]GACATTTAACATCCC | 59349 |
rs761439071 | snp | A/G | 1.64972e-05 | 0.00287199 | missense | KLHL12 | GRCh38.p7 | 1:202924981 | ACCTCACTAGTGAAC[A/G]TGGCACAGAAGTAAT | 59349 |
rs761466023 | snp | A/G | 1.73803e-05 | 0.00294785 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202893242 | CTAAATCCTCACCCT[A/G]CAATTGCATAGAGTC | 59349 |
rs761706946 | snp | C/G | 1.6549e-05 | 0.0028765 | intron-variant | KLHL12 | GRCh38.p7 | 1:202892662 | ATTACCATCATATCT[C/G]AGTGGGAAAGAAGCA | 59349 |
rs761722463 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202903930 | GCCCTGTCTCATGCA[C/T]TCTTATGAGCTCTTT | 59349 |
rs761740671 | snp | C/T | 1.65012e-05 | 0.00287234 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202911177 | CCAGTTGATGACAGC[C/T]TCAAAGACTGGCTCT | 59349 |
rs761748821 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202910090 | AATAAATAGTAGTAA[A/C]CACTTATGTACAAAG | 59349 |
rs761830667 | snp | C/T | 1.65266e-05 | 0.00287455 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911032 | TCAAGGTTTTGGATC[C/T]TGAGAGTGTTGCACT | 59349 |
rs761836218 | snp | C/T | 1.64879e-05 | 0.00287118 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894561 | TTACCCATTGAGTTC[C/T]CTCCCATTCCTGCAT | 59349 |
rs761840775 | in-del | -/TAAC | 1.64762e-05 | 0.00287016 | frameshift-variant | KLHL12 | GRCh38.p7 | 1:202911091 | TATACCTGGGGGTTA[-/TAAC]GTAGGGGCATCCGCA | 59349 |
rs761895301 | in-del | -/A | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202906456 | GCAACGCTTCGTCTC[-/A]AAAAAAAAAAAAAAA | 59349 |
rs762103315 | snp | A/T | 1.64735e-05 | 0.00286993 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202918249 | ATGCTGTACCACTTC[A/T]GGAAAATGCTTCTGG | 59349 |
rs762116855 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202899281 | AGCGCCACTACACTC[C/T]AGCCTGGGCAATAAG | 59349 |
rs762136459 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202919303 | GGAAAACAAACCACC[C/T]GTAATCCTGTGAAAA | 59349 |
rs762301676 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202921497 | TGCATTTAGTAATGA[C/T]GAAAAAGAACATGCA | 59349 |
rs762357759 | in-del | -/TTCCT | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202924315 | CATTAAAAACTCTTC[-/TTCCT]TTCATTTGAAGTTAT | 59349 |
rs762374851 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202906942 | GCTGGGATTACAGGT[A/G]TGAGACACCGTGCCC | 59349 |
rs762413525 | in-del | -/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926124 | AAAAAAAAAAAAAAA[-/G]AAACTTCAATTGAGG | 59349 |
rs762421379 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202892872 | CCTTTCCACACAAGT[C/T]CTTCATTAAGGCTGC | 59349 |
rs762482656 | snp | A/C | 1.65589e-05 | 0.00287736 | splice-acceptor-variant | KLHL12 | GRCh38.p7 | 1:202919909 | CCCCTTCTCTGAGAG[A/C]TGAAAATTCAAAAGG | 59349 |
rs762514226 | snp | A/G | 1.77972e-05 | 0.002983 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893223 | ATTGAGTCTGGATTC[A/G]TTTCTAAATCCTCAC | 59349 |
rs762601246 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926557 | TAGGGGTGTAAAAAG[G/T]TCTAGAACAAATGTC | 59349 |
rs762605028 | snp | A/G | 1.64933e-05 | 0.00287165 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202892643 | CAATGCTACTTAGCA[A/G]GGAATTACCATCATA | 59349 |
rs762614670 | snp | C/G | | | downstream-variant-500B, upstream-variant-2KB | KLHL12, RABIF | GRCh38.p7 | 1:202890896 | TAACTCCAAGCGTCA[C/G]AGGGGCTAATGAATA | 59349 |
rs762759632 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202909944 | ATTAAAAAAAACTCT[C/T]CTAAAATTGTCCTGT | 59349 |
rs762792577 | in-del | -/G | 1.6946e-05 | 0.00291079 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918123 | CTATTTGCAAGTTTT[-/G]TAATTGCCCAATCTT | 59349 |
rs762794430 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202901006 | AGCCGAGATCATGCC[A/G]CTACACTCCAGCCTG | 59349 |
rs762859511 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202909071 | AGGCCTCAGATGAAA[C/T]TTCTTTGCTTCATCA | 59349 |
rs762871580 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202915697 | GACTCTGGAGCCAGA[C/T]TACTCGAATTTGAAA | 59349 |
rs762880874 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202897113 | AATCATAAGGCTGTC[G/T]AATGGGGAGTTATTT | 59349 |
rs762905234 | snp | C/T | 1.73057e-05 | 0.00294152 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893452 | GAATGCATTAGCAAA[C/T]GTATGGTACTAAGCC | 59349 |
rs762987538 | snp | A/G | 1.64743e-05 | 0.00287 | missense | KLHL12 | GRCh38.p7 | 1:202918221 | CTCCTTGACTCAGAA[A/G]AATGAACTCTTCATG | 59349 |
rs762995740 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202899247 | AACCCAGGAAGTGGA[A/G]GTTGTAGTGAGCTGA | 59349 |
rs763045629 | snp | C/T | 1.64749e-05 | 0.00287005 | missense | KLHL12 | GRCh38.p7 | 1:202918329 | CAAAATCCCTAATAC[C/T]CAGGCAATTAGAAGG | 59349 |
rs763121009 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202898834 | TTTGAACAACATAAG[C/T]ACTCAAAAACAAACA | 59349 |
rs763156839 | in-del | -/TCTC | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911459 | ATATATATATGTATC[-/TCTC]TCTCTCTCTCTCTCT | 59349 |
rs763268602 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202924881 | TAAAAATTCAAAATT[A/G]TATCAAACTTCCACT | 59349 |
rs763448455 | in-del | -/AAAC | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202898841 | AACATAAGTACTCAA[-/AAAC]AAACAACAAAAAATT | 59349 |
rs763454909 | snp | A/T | 1.86816e-05 | 0.00305622 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895764 | TTTCAGTTAGGCAAG[A/T]TTTGGGCCTTACCTT | 59349 |
rs763518863 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202919035 | TGGGAGGATCACTCG[A/G]GCCCACGAGCTTGAG | 59349 |
rs763536806 | snp | A/G | 1.64798e-05 | 0.00287047 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202895599 | ACCCCATCCTCATCT[A/G]CTGTGTAGTCTAGAC | 59349 |
rs763544689 | snp | C/T | 1.66871e-05 | 0.00288847 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924952 | TTCATTTGTGTGGGG[C/T]TAATTTACCACTTAC | 59349 |
rs763559351 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202918757 | TCTACATGAAAACTT[A/C]CTAAAAGACTAGAGT | 59349 |
rs763714046 | snp | G/T | 1.65935e-05 | 0.00288036 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919917 | CTGAGAGCTGAAAAT[G/T]CAAAAGGTATAAAAG | 59349 |
rs763747560 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926591 | TTACTATGAAGACAG[C/G]CCGGGGGGTCTTTTA | 59349 |
rs763797716 | snp | C/T | 1.64789e-05 | 0.0028704 | missense | KLHL12 | GRCh38.p7 | 1:202919814 | TTCTCCACTGTCACA[C/T]GTACTGTTTCTGTGT | 59349 |
rs763863176 | snp | A/G | 1.64944e-05 | 0.00287175 | missense | KLHL12 | GRCh38.p7 | 1:202892645 | ATGCTACTTAGCAGG[A/G]AATTACCATCATATC | 59349 |
rs763877169 | snp | A/G | 1.65217e-05 | 0.00287412 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892525 | TCTGGATGGTGCTCC[A/G]ACAATGGTCACTTCT | 59349 |
rs763893056 | snp | C/T | 1.64751e-05 | 0.00287007 | missense | KLHL12 | GRCh38.p7 | 1:202909076 | TCAGATGAAACTTCT[C/T]TGCTTCATCAACCAG | 59349 |
rs763950903 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202901105 | ATTCAGGCACCTTTT[A/G]AAGGGTGGGAGAAAA | 59349 |
rs763957361 | snp | A/G | 1.65474e-05 | 0.00287636 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911019 | AGGTAAGAGTCCGTC[A/G]AGGTTTTGGATCCTG | 59349 |
rs764021448 | in-del | -/CATTCTTGTTTTTTTTTTCTTTTTTGAGACAAGGTCTTGCTCTGC | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202903453 | ATTGTTTCTCTCATG[lengthTooLong]TGCCCAGGCTAGAGT | 59349 |
rs764103704 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202902198 | GCACTTTGGGAGGCT[A/G]AGATGAGTGGATCAC | 59349 |
rs764153272 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202896133 | TTGGATTTCCATGTT[A/T]TCTCAGAAATTACTA | 59349 |
rs764170373 | snp | A/G | 0.000120489 | 0.0077608 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928455 | CTTAATATGCCAAGC[A/G]TCTGATTGCAGCAAG | 59349 |
rs764242619 | snp | A/G | 0.00010433 | 0.00722177 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893458 | ATTAGCAAATGTATG[A/G]TACTAAGCCTAGAAT | 59349 |
rs764261228 | snp | C/T | 3.32209e-05 | 0.00407546 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911234 | TACACACCGTGGATC[C/T]TACTTTTCCAATTAG | 59349 |
rs764324337 | snp | A/C | 1.64741e-05 | 0.00286998 | missense | KLHL12 | GRCh38.p7 | 1:202918234 | AAGAATGAACTCTTC[A/C]TGCTGTACCACTTCA | 59349 |
rs764442253 | in-del | -/ATTTT | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904370 | ATAATTTTGTATATG[-/ATTTT]TTTATTTATTCAAAT | 59349 |
rs764495932 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202906854 | TTTAGTAGACATGGG[A/G]TTTCACCATGTTGGC | 59349 |
rs764515708 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202914096 | AATATGAAGCTGGAG[A/T]GTTAAGCAAGGGCCA | 59349 |
rs764626301 | snp | A/G | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891433 | AGGAAAACTTATAGC[A/G]GAAAAAAGACTAGAT | 59349 |
rs764643744 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911958 | TGTGGTAATGAGAGA[A/C]CCAAACACCAAGTGC | 59349 |
rs764679282 | snp | C/G | 1.64819e-05 | 0.00287066 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896803 | TGATCTGGAGGCAGA[C/G]ACTGAGGACATTTAA | 59349 |
rs764766586 | in-del | -/A | | | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929758 | TTTGGAGACTGAAGC[-/A]AGGAAGATTGCTTGA | 59349 |
rs764850717 | snp | A/G/T | 4.96055e-05 | 0.00498003 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892518 | CACTAGCTCTGGATG[A/G/T]TGCTCCAACAATGGT | 59349 |
rs764908987 | snp | A/G | | | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929218 | ATGTCATACCTTCCT[A/G]ATCTAAAACTGTCCC | 59349 |
rs764910797 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202900978 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 59349 |
rs764932289 | snp | C/T | 1.64738e-05 | 0.00286995 | missense | KLHL12 | GRCh38.p7 | 1:202909060 | CTCCGAAGTTCAGGC[C/T]TCAGATGAAACTTCT | 59349 |
rs764995481 | snp | C/T | | | intron-variant, utr-variant-5-prime | KLHL12 | GRCh38.p7 | 1:202927160 | AGTGCGGCGCGGGGC[C/T]AGCAGGCGGCTCGGG | 59349 |
rs765042033 | snp | C/G | 1.64795e-05 | 0.00287045 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202925154 | TTTGGGGGCCATAAT[C/G]CCTCCCATAAAGCAG | 59349 |
rs765094063 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202902424 | AACAGAGCGAGACTC[C/T]GTCCAAAAAAAAAAA | 59349 |
rs765142138 | snp | C/T | 1.84497e-05 | 0.00303719 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894325 | AGTGGTAAATCCTCA[C/T]GCCCATTCCTGGTCG | 59349 |
rs765155347 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202913138 | CGCACTATGCTATTT[C/G]AGAAGATATATTTAA | 59349 |
rs765244944 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202899922 | ATGTCTGCCTAAAAT[G/T]ACTTCAAGTTGGGAG | 59349 |
rs765321433 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202894098 | TCATTTTTACATTAA[C/T]CTACGGTTTGTCCCA | 59349 |
rs765371523 | snp | G/T | 9.93888e-05 | 0.00704872 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911212 | AATCCACCTGTAAAT[G/T]TATAATTACACACCG | 59349 |
rs765401722 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202894151 | AGGTCTGACAGCATC[A/G]CCTATTGTCCCCTCC | 59349 |
rs765483737 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202905995 | TTTTTTTTTTTTTGT[A/T]TTTTTAGTAGATACG | 59349 |
rs765526918 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202909942 | TTATTAAAAAAAACT[A/C]TTCTAAAATTGTCCT | 59349 |
rs765676318 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904242 | CTCCCGATCTCAGGT[G/T]ATCCACCTGCCTCAG | 59349 |
rs765723956 | snp | A/G | 1.66874e-05 | 0.0028885 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894762 | TATCTGCTCAGAATA[A/G]ACAAATTACAGACTA | 59349 |
rs765728680 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202913847 | GCTATTTACATTCAC[C/T]GTAATTAAAACTAAA | 59349 |
rs765764310 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202905512 | AAAAATCAAAGTAAG[A/C]AAAATGTCTTATCTC | 59349 |
rs765771585 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911330 | ATTTCCCATCTTCCA[G/T]AAATAGCTAGGCTCT | 59349 |
rs765786597 | snp | A/G | 3.30797e-05 | 0.00406679 | missense | KLHL12 | GRCh38.p7 | 1:202919904 | GGTTTCCCCTTCTCT[A/G]AGAGCTGAAAATTCA | 59349 |
rs765884319 | snp | A/G | 8.24192e-05 | 0.00641894 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202919774 | CAACTGAAGCAGACA[A/G]GCTGCAGGAAGCAGT | 59349 |
rs765898152 | snp | A/G | 1.65228e-05 | 0.00287422 | intron-variant | KLHL12 | GRCh38.p7 | 1:202897006 | AGTTCAGCATCCCTG[A/G]ATGGGTAACTAGTCA | 59349 |
rs765973031 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904085 | GTGCAATGGCACGAT[C/T]TTGGTTCACCACAAT | 59349 |
rs766058465 | snp | G/T | 3.29484e-05 | 0.00405871 | missense | KLHL12 | GRCh38.p7 | 1:202925135 | GAGTATTTGTCATTA[G/T]GTCTTTGGGGGCCAT | 59349 |
rs766067781 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202912765 | CTGGAGAGGAGAGCC[A/G]GAGAAGTGACAGGGA | 59349 |
rs766094982 | snp | A/G | 8.23784e-05 | 0.00641735 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896837 | CCCTCCCAACGAATG[A/G]TTTCACCATTATTTA | 59349 |
rs766148239 | snp | A/C | 3.29516e-05 | 0.00405891 | missense | KLHL12 | GRCh38.p7 | 1:202925011 | TCACTACAGGCAGCC[A/C]GCACAATCCGATGGG | 59349 |
rs766250259 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202897501 | AGTGCTGGGATTACA[G/T]GTGTGAGTCACTGTG | 59349 |
rs766348045 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202899424 | ACATATACACTCACA[C/T]ATAAACCACGGAGTT | 59349 |
rs766399420 | snp | A/G | 1.71437e-05 | 0.00292772 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893441 | CTGGGGAAAATGAAT[A/G]CATTAGCAAATGTAT | 59349 |
rs766428782 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202908648 | AGGGGAAGTGAAGAG[A/G]TGGGTGGAAGCATAT | 59349 |
rs766457945 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202920842 | ATATTAAAATACAGA[C/T]GTATTTACAGAATAG | 59349 |
rs766492426 | snp | A/G | 1.65097e-05 | 0.00287308 | stop-gained, intron-variant | KLHL12 | GRCh38.p7 | 1:202893291 | CCCCTACATAGCATC[A/G]TGGAGTGGTCATACT | 59349 |
rs766515278 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202893762 | AGTTGTGATTATGGT[C/T]CTGAAGCAATTTTTA | 59349 |
rs766546425 | in-del | -/T | 1.67351e-05 | 0.00289263 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919706 | TATTAATTTTCAACC[-/T]TTCCAGGGCTATTTT | 59349 |
rs766654277 | in-del | -/TAAG | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202920761 | TCTATACGCCAGGAA[-/TAAG]TAATAGGTAACACCT | 59349 |
rs766654299 | snp | A/G | 1.66197e-05 | 0.00288263 | missense | KLHL12 | GRCh38.p7 | 1:202894746 | CCAGAGACATAGATC[A/G]TATCTGCTCAGAATA | 59349 |
rs766665146 | snp | C/G | 1.65176e-05 | 0.00287376 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919749 | AGCAAGTTTTAATGT[C/G]TGTACCTTTCAACTG | 59349 |
rs766734100 | snp | A/G | 1.64754e-05 | 0.00287009 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202894598 | CTCAATACCTAGACA[A/G]TAGATCACTCCACTG | 59349 |
rs766739292 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202893886 | CTACTCTTTTGTCCT[G/T]ATGCATTAGAGACTT | 59349 |
rs766861946 | snp | A/G | 1.65658e-05 | 0.00287795 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918407 | GGACAGACACAGGCA[A/G]CAAACACTTTAGAAT | 59349 |
rs766887247 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202895460 | CCAGACAACAGGAGA[C/G]GTTAAAAACCCTGGT | 59349 |
rs766970061 | snp | A/T | 1.65693e-05 | 0.00287826 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892497 | CTAACTGTCCACTGG[A/T]CTGGTCACTAGCTCT | 59349 |
rs767019738 | snp | C/T | | | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202930101 | AGTGAGCTGAGATCA[C/T]GCCACTGCACTCCAG | 59349 |
rs767029819 | snp | C/T | 1.64958e-05 | 0.00287187 | missense | KLHL12 | GRCh38.p7 | 1:202924982 | CCTCACTAGTGAACA[C/T]GGCACAGAAGTAATC | 59349 |
rs767135855 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202914669 | TCAGGAGTTTGAGAC[A/G]AGCCTGGCCAAGATG | 59349 |
rs767243939 | snp | G/T | 1.6617e-05 | 0.00288239 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919924 | CTGAAAATTCAAAAG[G/T]TATAAAAGAATGATG | 59349 |
rs767290300 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202922428 | AAAAATTAGCCAGGC[A/G]TCAAGGAAAAAAAAA | 59349 |
rs767334505 | snp | A/G | 6.64132e-05 | 0.00576213 | intron-variant | KLHL12 | GRCh38.p7 | 1:202892672 | TATCTGAGTGGGAAA[A/G]AAGCAAAAGAAAGAA | 59349 |
rs767407064 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202924841 | GTGGTAGATCTTATC[C/T]AGAATCTGCCAAAAC | 59349 |
rs767472065 | in-del | -/CCTAGTT | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202920981 | GTCTCTCCAGGACTA[-/CCTAGTT]CCTATCATCTGTCCT | 59349 |
rs767541754 | snp | C/G | 1.65143e-05 | 0.00287348 | missense | KLHL12 | GRCh38.p7 | 1:202911185 | TGACAGCCTCAAAGA[C/G]TGGCTCTTCAGAATC | 59349 |
rs767599252 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202923850 | TCTACACTAAGATGA[C/T]AGAACTAACTAAAAA | 59349 |
rs767628380 | in-del | -/A | 1.64732e-05 | 0.0028699 | frameshift-variant | KLHL12 | GRCh38.p7 | 1:202925098 | TGAGGGAGTTCATTG[-/A]AATTGAGGATGGATT | 59349 |
rs767629892 | snp | A/G | 1.65179e-05 | 0.00287379 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911036 | GGTTTTGGATCCTGA[A/G]AGTGTTGCACTACTT | 59349 |
rs767702820 | snp | A/C | 4.94515e-05 | 0.00497225 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894566 | CATTGAGTTCCCTCC[A/C]ATTCCTGCATCCCAG | 59349 |
rs767797106 | snp | A/G | 1.6519e-05 | 0.00287388 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918393 | TTGTTTCACACCTAG[A/G]ACAGACACAGGCAGC | 59349 |
rs767843978 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202893074 | TGGGTGACAGAGCAA[C/T]ACTCTGTCTCTAAAA | 59349 |
rs767885142 | snp | C/T | 0.000164726 | 0.0090739 | missense | KLHL12 | GRCh38.p7 | 1:202918256 | ACCACTTCAGGAAAA[C/T]GCTTCTGGCTAAAAA | 59349 |
rs767896636 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202893600 | ATTCCATCTATAAAC[C/G]CTTTGGCTTGGACTT | 59349 |
rs767915255 | snp | A/C | | | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928357 | GCAGGGAGCCTGGGA[A/C]TGTATCTACAGCTCG | 59349 |
rs768160708 | snp | C/T | 1.77855e-05 | 0.00298202 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893224 | TTGAGTCTGGATTCG[C/T]TTCTAAATCCTCACC | 59349 |
rs768192806 | in-del | -/G | 1.6489e-05 | 0.00287128 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896972 | GCTCCTGAAGACAAA[-/G]GCAGAAAAAAGATGG | 59349 |
rs768195107 | snp | C/T | | | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929778 | AGATTGCTTGAGCCC[C/T]GAAGTTCGTGACCAG | 59349 |
rs768197068 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202923975 | TTATATAATAAACAG[C/T]GATGCACCCACAACT | 59349 |
rs768233955 | snp | C/T | 1.65217e-05 | 0.00287412 | synonymous-codon, intron-variant | KLHL12 | GRCh38.p7 | 1:202893382 | TGTACCATCAAATCC[C/T]CCCACCACATAAATA | 59349 |
rs768252677 | snp | A/G | 1.6489e-05 | 0.00287128 | missense | KLHL12 | GRCh38.p7 | 1:202911164 | TGGCATGCTTCACCC[A/G]GTTGATGACAGCCTC | 59349 |
rs768261962 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202920425 | ACTGTTTCCCAGGCT[A/G]GAGTGCAGTGGTGCC | 59349 |
rs768266282 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202918076 | CAAAATGCACACTTA[A/G]TTATGAAGCCCTGAT | 59349 |
rs768282709 | in-del | -/TAATAAT | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202899841 | AAAAAAAAAAAAAAA[-/TAATAAT]AATAAATAAAAAAAT | 59349 |
rs768323824 | snp | C/T | 1.64912e-05 | 0.00287147 | missense | KLHL12 | GRCh38.p7 | 1:202918176 | AAATCCGTACCTGAA[C/T]TTCGTCGCACTTGAT | 59349 |
rs768366493 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202909388 | GTATTTCCCATCTAT[C/T]GCAGCGCTTACATTT | 59349 |
rs768414361 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202912467 | GACAGCCGTGGTGGT[A/G]GTGGTGGATATGGTG | 59349 |
rs768494700 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904994 | AAGAGTCATTATCCT[A/G]GTAGCTGGTTTAGCA | 59349 |
rs768513281 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202915951 | TAAGTGAACCAACAG[C/T]AAATGCTGAATAAGT | 59349 |
rs768583903 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202898912 | ATTGTGTGATTTTAA[A/T]CAGTGATAATGGCAT | 59349 |
rs768599246 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202917226 | ATTATTCCTTCTTCC[C/G]CCGCAAGAGACAGGG | 59349 |
rs768701651 | in-del | -/GTTCAAGT | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202921105 | ACCTCTGCCTCCCAG[-/GTTCAAGT]GTTCAAGTGTTTCTC | 59349 |
rs768780357 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926941 | TGACCGAGGCCAGAT[A/G]CCCCACCCCACTGCC | 59349 |
rs768857530 | in-del | -/TATC | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202903976 | AACCCTTTAACCCTT[-/TATC]TATCTATCTATCTAT | 59349 |
rs769085231 | snp | G/T | 4.94368e-05 | 0.00497152 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202909014 | TACCAGCTTACCTAG[G/T]CGAGCCCTTGTCCTG | 59349 |
rs769130565 | in-del | -/AT | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202924679 | AATCCAATAGCTGAC[-/AT]GTGTGTTTTACTACA | 59349 |
rs769175837 | in-del | -/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202922491 | AAGAAGATCCAAGAC[-/T]TTTTTTTTTTTTTGA | 59349 |
rs769177103 | snp | A/C | 6.59435e-05 | 0.00574172 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896964 | CTTCATTGGCTCCTG[A/C]AGACAAAGGCAGAAA | 59349 |
rs769262365 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202919972 | TAAAGGCAGAATCTC[A/C]TATCTAAGAGCTTAG | 59349 |
rs769267863 | in-del | -/CT | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202903918 | CCACTGCTCTTGGCC[-/CT]GTCTCATGCATTCTT | 59349 |
rs769320889 | snp | A/C | 4.94442e-05 | 0.00497188 | missense, utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892625 | TGATAGGGTCATAAC[A/C]TTCAATGCTACTTAG | 59349 |
rs769329110 | snp | C/T | 3.29609e-05 | 0.00405948 | missense | KLHL12 | GRCh38.p7 | 1:202911146 | ATTCTTCCCGCTCTT[C/T]CTTGGCATGCTTCAC | 59349 |
rs769356851 | snp | A/T | 1.66175e-05 | 0.00288244 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924959 | GTGTGGGGCTAATTT[A/T]CCACTTACCTCACTA | 59349 |
rs769395775 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202908115 | ACCTAGGCTTTTGGA[C/T]AGTGAAGCAAAGAGA | 59349 |
rs769397973 | snp | G/T | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891836 | TCAAATAATATACCC[G/T]TCTCAGTCTTCCAGG | 59349 |
rs769453171 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202918596 | GCAAGACCTTTACAC[A/C]TGTCTCTGCTTAATC | 59349 |
rs769487910 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202893119 | AATAAAAAAAATCAA[A/G]TTGCCACTGGAGATG | 59349 |
rs769501532 | snp | A/G | 0.000116728 | 0.00763874 | synonymous-codon, intron-variant | KLHL12 | GRCh38.p7 | 1:202895528 | CCAGCCTACCTCCCA[A/G]GGTGGTGGCTCCAGC | 59349 |
rs769548541 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202915592 | CTGTATAGTTCCAAA[A/T]GAAATGACTTCTATG | 59349 |
rs769641380 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202914252 | TAGAACAGTTTAAAG[A/G]GCCAAGAGCTAGAAG | 59349 |
rs769642679 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202916733 | TTAGAGGCTTTCTTT[A/G]AATGGTATTGCCTGA | 59349 |
rs769737790 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911211 | GAATCCACCTGTAAA[C/T]GTATAATTACACACC | 59349 |
rs769743265 | snp | A/G | 1.65119e-05 | 0.00287327 | missense | KLHL12 | GRCh38.p7 | 1:202894704 | TAGCGCTCCATACTG[A/G]TGTGACGCCTGCTTC | 59349 |
rs769748536 | snp | A/G | | | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929409 | ATCAACAACAACATT[A/G]AATGTCCATTAATAG | 59349 |
rs769791759 | in-del | -/TTC | 1.64776e-05 | 0.00287028 | cds-indel | KLHL12 | GRCh38.p7 | 1:202911131 | CAGGTTAGGCAAGGA[-/TTC]TTCTTCCCGCTCTTT | 59349 |
rs769829965 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202897086 | TGAGGGATGCAATCC[A/G]AAATGGGAGATAATC | 59349 |
rs769833084 | snp | A/C | 1.66283e-05 | 0.00288338 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919727 | GGGCTATTTTGACAT[A/C]AACAATAGCAAGTTT | 59349 |
rs769880715 | snp | A/C | 1.64779e-05 | 0.00287031 | synonymous-codon, intron-variant | KLHL12 | GRCh38.p7 | 1:202896944 | GCCCCCAACCACCAA[A/C]AGCACTTCATTGGCT | 59349 |
rs769969524 | snp | A/C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202925975 | CCAGGCGTGGTGATG[A/C/T]GCGCCTATAATCCTA | 59349 |
rs770009564 | in-del | -/TT | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202921177 | ACTACAACCAGCTAA[-/TT]TTTTTTTTTTTTTTT | 59349 |
rs770168346 | in-del | -/TT | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202919542 | GGTGCAAATGCTCTC[-/TT]TTATAGAGCCAAATA | 59349 |
rs770201887 | snp | A/T | 1.64732e-05 | 0.0028699 | missense | KLHL12 | GRCh38.p7 | 1:202925061 | TACTCTCAATGTCAC[A/T]TCACAGAGGGTATTG | 59349 |
rs770278043 | snp | C/T | 3.29614e-05 | 0.00405951 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202893351 | TGTTGTATGCTTCAA[C/T]GGAAGAAAGGTGGGC | 59349 |
rs770285405 | snp | C/G | 6.71987e-05 | 0.0057961 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924939 | GAGTTCCACGGGTTT[C/G]ATTTGTGTGGGGCTA | 59349 |
rs770344551 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202898788 | GAGACATGAAATCAC[A/G]AGCAACGTGTGGACT | 59349 |
rs770407297 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202906607 | TTAACATGAGTCAAC[C/T]GTACATGTAAAAATG | 59349 |
rs770431123 | snp | C/T | 1.64743e-05 | 0.00287 | missense | KLHL12 | GRCh38.p7 | 1:202909048 | CCCTGCATCTGACTC[C/T]GAAGTTCAGGCCTCA | 59349 |
rs770444708 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202905227 | TAACCAAGCAGGAGC[C/T]CCTTCTGCTGCCTGT | 59349 |
rs770521328 | snp | A/G | 1.87954e-05 | 0.00306551 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925221 | AACTACAAGAGGGAA[A/G]AAAAAACAATGAGCA | 59349 |
rs770560309 | in-del | -/A | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904369 | ATAATTTTGTATATG[-/A]ATTTTTTTATTTATT | 59349 |
rs770710185 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202892972 | GCTTGAGCCCAGGAG[C/T]TGGAGACCAGCCTAG | 59349 |
rs770733365 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202918902 | ATGTATTAAAAACTA[A/C]AAGTGTGTCAATTAT | 59349 |
rs770744955 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202918069 | TTTGAGCCAAAATGC[A/G]CACTTAATTATGAAG | 59349 |
rs770788218 | snp | C/T | 1.64866e-05 | 0.00287106 | stop-gained | KLHL12 | GRCh38.p7 | 1:202894668 | TCTCCCAGCATGCTC[C/T]ACTGGTCAATGTTTG | 59349 |
rs770805929 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926323 | GGGGGAAGGAAATCA[A/C]ACTGTGGTCTCCAAA | 59349 |
rs770830744 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202914111 | AGTTAAGCAAGGGCC[A/C]GGTACAGAGAGCATT | 59349 |
rs770877593 | snp | C/G | 1.64743e-05 | 0.00287 | missense | KLHL12 | GRCh38.p7 | 1:202918314 | AATTGTGGGTTTCAG[C/G]AAAATCCCTAATACC | 59349 |
rs770884383 | snp | A/G | 0.000177794 | 0.00942683 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894293 | TCCTCCTGGAAGACA[A/G]AGACCATTCCAGAAA | 59349 |
rs770944885 | snp | A/T | 1.72868e-05 | 0.00293992 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895732 | TCTATGGATTTGGAG[A/T]GAAGAGGTACAGAGC | 59349 |
rs771036525 | snp | A/C/G | 0.00011783 | 0.00767483 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924933 | CAACTAGAGTTCCAC[A/C/G]GGTTTCATTTGTGTG | 59349 |
rs771066732 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202909763 | GTCAAGGTTTCTCTC[A/G]AGGCAGTGACTCTAC | 59349 |
rs771071486 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202903729 | CTGGGCTAAAATGAT[C/T]CTCCTGCCTCAACCT | 59349 |
rs771074229 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911749 | TTTCAAAAGCATTAT[C/T]GCCTTTCTGCCTGTG | 59349 |
rs771118191 | snp | C/G | 3.29794e-05 | 0.00406061 | synonymous-codon, intron-variant | KLHL12 | GRCh38.p7 | 1:202895568 | TCGGACATTCATAGG[C/G]GCCACAGAATACCAG | 59349 |
rs771228717 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202898390 | TACCTTGAAGCTGAC[A/C]GGAAACACAGATAAA | 59349 |
rs771251724 | snp | A/T | 1.64866e-05 | 0.00287106 | stop-gained | KLHL12 | GRCh38.p7 | 1:202919885 | ACCTTGGATGTCAAC[A/T]TAAGGTTTCCCCTTC | 59349 |
rs771314667 | snp | A/G | 1.6477e-05 | 0.00287024 | missense, utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892594 | CCCATGGATGTCACG[A/G]CTTCCCAGCTGTCGA | 59349 |
rs771352133 | snp | C/T | 1.79348e-05 | 0.00299451 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893207 | CTTGCTCTGGCTACA[C/T]ATTGAGTCTGGATTC | 59349 |
rs771481964 | snp | A/T | 1.66286e-05 | 0.0028834 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909161 | AGTTAGGCACTGGGG[A/T]TACCTGTAATACTAT | 59349 |
rs771586916 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202917290 | TGCGATCATGGCTCA[C/T]TGCAGCCTCAAACTC | 59349 |
rs771597257 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202897544 | GCACCATTTCAACCT[A/T]TTGAGATGACTGGCT | 59349 |
rs771676740 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202903935 | GTCTCATGCATTCTT[A/C]TGAGCTCTTTACACA | 59349 |
rs771680562 | snp | A/C | 1.65438e-05 | 0.00287605 | synonymous-codon, intron-variant | KLHL12 | GRCh38.p7 | 1:202893388 | ATCAAATCCCCCCAC[A/C]ACATAAATATGGTCA | 59349 |
rs771726087 | snp | A/G | 3.47959e-05 | 0.00417094 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202894254 | GTATTTCTCAACTGA[A/G]TTTAAGATATTCAAG | 59349 |
rs771735163 | in-del | -/CCCATTA | 1.65051e-05 | 0.00287267 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894542 | AATCCTTACCCACAG[-/CCCATTA]CCCATTGAGTTCCCT | 59349 |
rs771829319 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202913253 | TCACTGGAAGGACTT[A/C]GGTATATAATAACAC | 59349 |
rs771900812 | snp | C/G | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891547 | TAGGCTACTGTCACT[C/G]CCAGCCCATCCCCAA | 59349 |
rs771906559 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202918290 | CAGCTGCTTGCATCA[A/G]GTCAACACAATTGTG | 59349 |
rs772082575 | snp | A/G | 1.65389e-05 | 0.00287562 | synonymous-codon, intron-variant | KLHL12 | GRCh38.p7 | 1:202895547 | GGTGGCTCCAGCAAG[A/G]CCTCGTCGGACATTC | 59349 |
rs772172467 | snp | A/G | 1.65693e-05 | 0.00287826 | missense | KLHL12 | GRCh38.p7 | 1:202894734 | CCATCAAAGCCTCCA[A/G]AGACATAGATCATAT | 59349 |
rs772197632 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202915124 | TCACAAAGAATTCTC[C/T]TGAGTATTAGGTACT | 59349 |
rs772239694 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202902247 | CCAGCCTGGCCAACA[C/T]GGTGAAACCCCATCT | 59349 |
rs772260431 | snp | A/T | 1.65575e-05 | 0.00287724 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919738 | ACATAAACAATAGCA[A/T]GTTTTAATGTCTGTA | 59349 |
rs772305070 | in-del | -/GGA | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202906491 | AAAGTTCCTACCCTG[-/GGA]GGAGGAAAGGCAAAA | 59349 |
rs772381045 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202895429 | CTTAATTTTTTCTCC[A/G]TATTTCATGCTCCTG | 59349 |
rs772389361 | in-del | -/TTTTTTTTTTTTT | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202903616 | AGCTGGGACCACTAA[-/TTTTTTTTTTTTT]TTTTTTTCTTTTCTT | 59349 |
rs772397033 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202909628 | TCTTTCATTTGCCTC[C/T]CAACTCACTCTGTAC | 59349 |
rs772486643 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202910842 | ACAAAATTGAACCAC[A/G]GATTTTCATTTGTGT | 59349 |
rs772507937 | snp | C/T | 1.6477e-05 | 0.00287024 | missense, utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892592 | TTCCCATGGATGTCA[C/T]GACTTCCCAGCTGTC | 59349 |
rs772518399 | snp | A/G | 1.65649e-05 | 0.00287788 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909147 | ATAGCAGACAGCAGA[A/G]TTAGGCACTGGGGAT | 59349 |
rs772519697 | snp | A/G | 1.73375e-05 | 0.00294422 | synonymous-codon, utr-variant-5-prime | KLHL12 | GRCh38.p7 | 1:202925207 | TCCTTGGATTCTGCA[A/G]CTACAAGAGGGAAAA | 59349 |
rs772597619 | snp | A/T | 1.65809e-05 | 0.00287926 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892485 | TTGATTCTCCCACTA[A/T]CTGTCCACTGGACTG | 59349 |
rs772786410 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202918656 | ATCCAGAGACCTGGC[A/C]CAATTCAACAAAAAT | 59349 |
rs772795134 | snp | A/C | 1.64735e-05 | 0.00286993 | missense | KLHL12 | GRCh38.p7 | 1:202925118 | GAGGATGGATTTAGC[A/C]TGAGTATTTGTCATT | 59349 |
rs772799894 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202917621 | CACTTCCAAACTTTT[C/G]TCTCTTCATTTCTGA | 59349 |
rs772893807 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926227 | GCTCTTCAACAAGAG[A/G]GTATTCCTACTCTAC | 59349 |
rs772899805 | in-del | -/A | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202914866 | GCGAAACTCCGTCTA[-/A]AAAAAAAAAAAAAAA | 59349 |
rs772978994 | in-del | -/AT | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892434 | TGTAATCACCCGGTG[-/AT]CACATAGTGAGAAAC | 59349 |
rs773067521 | in-del | -/C | | | downstream-variant-500B, upstream-variant-2KB | KLHL12, RABIF | GRCh38.p7 | 1:202890885 | CTTTTTCAAGTAACT[-/C]CCAAGCGTCAGAGGG | 59349 |
rs773157193 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202905179 | TAGATTTATAGTTTA[A/G]TCCCTTAAGGTCAGG | 59349 |
rs773158440 | in-del | -/C | 3.3168e-05 | 0.00407221 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911223 | AAATGTATAATTACA[-/C]ACCGTGGATCCTACT | 59349 |
rs773312387 | snp | G/T | 1.6517e-05 | 0.00287372 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202911186 | GACAGCCTCAAAGAC[G/T]GGCTCTTCAGAATCC | 59349 |
rs773316341 | in-del | -/A | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926156 | CCATTACCTACACTG[-/A]AATAATGGAAACCAC | 59349 |
rs773437329 | snp | A/G/T | 3.29545e-05 | 0.00405911 | synonymous-codon, utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892593 | TCCCATGGATGTCAC[A/G/T]ACTTCCCAGCTGTCG | 59349 |
rs773446760 | snp | A/G | 1.65523e-05 | 0.00287678 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919739 | CATAAACAATAGCAA[A/G]TTTTAATGTCTGTAC | 59349 |
rs773637552 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202897776 | GGTCTCGCTATATTG[C/T]CCAGGCTGATCTCAA | 59349 |
rs773644046 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202893637 | ATAAAAGATAAATAA[C/T]AAAAATGGTTCTCTT | 59349 |
rs773671503 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202908449 | ACAGGCAGGTGCTAC[A/G]ATGATTCCATTTACA | 59349 |
rs773701757 | snp | A/G | 1.65798e-05 | 0.00287917 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892488 | ATTCTCCCACTAACT[A/G]TCCACTGGACTGGTC | 59349 |
rs773746245 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202915964 | AGTAAATGCTGAATA[A/C]GTATTAGCTATTATA | 59349 |
rs773919798 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202895343 | AGGCTGCAGTGAGCC[A/G]TGATCACACCACTGC | 59349 |
rs773938287 | snp | A/C | | | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929915 | TTCGAGAGGCCGAGG[A/C]GGGCGGATCACCTGA | 59349 |
rs774009398 | snp | A/T | | | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202893252 | ACCCTGCAATTGCAT[A/T]GAGTCTCCCCCGAAG | 59349 |
rs774099680 | snp | C/G | 1.65449e-05 | 0.00287614 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911022 | TAAGAGTCCGTCAAG[C/G]TTTTGGATCCTGAGA | 59349 |
rs774101004 | snp | A/C | 1.76714e-05 | 0.00297244 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893233 | GATTCGTTTCTAAAT[A/C]CTCACCCTGCAATTG | 59349 |
rs774193240 | snp | C/T | 1.64893e-05 | 0.0028713 | missense | KLHL12 | GRCh38.p7 | 1:202911166 | GCATGCTTCACCCAG[C/T]TGATGACAGCCTCAA | 59349 |
rs774227881 | in-del | -/GTC | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904219 | ATGTTGGTCAGGCTG[-/GTC]TCAAACTCCCGATCT | 59349 |
rs774230857 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202902581 | AGGGTTTATAATTTT[A/G]GGTTATAAACAATCA | 59349 |
rs774291134 | in-del | -/TTCAGT | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202896547 | CAATTTAACATTCAG[-/TTCAGT]TTAACACAGCACGAC | 59349 |
rs774301036 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202917229 | ATTCCTTCTTCCCCC[A/G]CAAGAGACAGGGTCT | 59349 |
rs774318971 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202903873 | ATCGCCTGCCTCAGC[C/G]TCTCAAAGTGCTGGG | 59349 |
rs774413122 | snp | A/T | 1.66015e-05 | 0.00288105 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919731 | TATTTTGACATAAAC[A/T]ATAGCAAGTTTTAAT | 59349 |
rs774482678 | snp | C/T | 1.64942e-05 | 0.00287173 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894551 | CCACAGCCCATTACC[C/T]ATTGAGTTCCCTCCC | 59349 |
rs774502549 | snp | C/T | 1.64768e-05 | 0.00287021 | missense | KLHL12 | GRCh38.p7 | 1:202918346 | AGGCAATTAGAAGGG[C/T]CCAACTGACTTTCTA | 59349 |
rs774660269 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202920193 | GTGGCACATGCCTGT[A/G]GTCCCAGCTACTCAG | 59349 |
rs774767279 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202913785 | CAGACAGAAGAGCAC[A/G]CTAAAAAGCACTAGA | 59349 |
rs774894949 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202921466 | AGGCGTGAGCCACCA[C/T]GCCCGGCCCTTAGAC | 59349 |
rs774940977 | snp | C/T | 1.64822e-05 | 0.00287068 | missense | KLHL12 | GRCh38.p7 | 1:202911152 | CCCGCTCTTTCTTGG[C/T]ATGCTTCACCCAGTT | 59349 |
rs774946172 | snp | A/T | 1.64732e-05 | 0.0028699 | missense | KLHL12 | GRCh38.p7 | 1:202925086 | GTATTGCTCTTCCTG[A/T]GGGAGTTCATTGAAT | 59349 |
rs774964356 | snp | C/T | 0.00010699 | 0.00731325 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893222 | TATTGAGTCTGGATT[C/T]GTTTCTAAATCCTCA | 59349 |
rs774997173 | snp | C/G | | | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927396 | AATTACAAAAAGGTC[C/G]GGTGGGCAGGGAATG | 59349 |
rs775023096 | snp | A/G | 1.64811e-05 | 0.00287059 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896808 | TGGAGGCAGAGACTG[A/G]GGACATTTAACATCC | 59349 |
rs775054022 | snp | C/T | 1.64811e-05 | 0.00287059 | synonymous-codon, utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892626 | GATAGGGTCATAACA[C/T]TCAATGCTACTTAGC | 59349 |
rs775151372 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202902413 | CCAGCCTGGGTAACA[A/G]AGCGAGACTCCGTCC | 59349 |
rs775177088 | in-del | -/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202903299 | TAGTTTTTAAATCTC[-/T]TGACACTCTGGTAGG | 59349 |
rs775204421 | snp | A/G | 0.000120985 | 0.00777675 | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202928443 | AGAATTCCAACGCTT[A/G]ATATGCCAAGCATCT | 59349 |
rs775208036 | snp | A/C | | | downstream-variant-500B, upstream-variant-2KB | KLHL12, RABIF | GRCh38.p7 | 1:202890844 | TTCAAGCGCGTGCTA[A/C]GTGAATTCAAGATCT | 59349 |
rs775243684 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202906747 | GCTCACTGCAACCTC[C/T]GCCTCCCGGGTTCAA | 59349 |
rs775278518 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202907511 | GGAGTCTGAGGCACA[A/G]GAATTGCTTGAACCT | 59349 |
rs775330084 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202908261 | CTCTCATCTTAGTGG[C/T]AGACATACAGGCTCA | 59349 |
rs775332302 | snp | C/T | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892036 | CCTCTAGAATGGAAC[C/T]GTGTTGCCCCTAGCT | 59349 |
rs775369295 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202914257 | CAGTTTAAAGGGCCA[A/C]GAGCTAGAAGAGGTT | 59349 |
rs775371725 | snp | G/T | | | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929662 | GTAATTTATTTTGCC[G/T]TTTGAATTTTGCTTC | 59349 |
rs775461630 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202915604 | AAAAGAAATGACTTC[C/T]ATGATTATTTCCTGA | 59349 |
rs775562645 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202925957 | TAAAAATACAAAAAA[A/T]AGCCAGGCGTGGTGA | 59349 |
rs775574151 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202923716 | TAAAATGAGATGGTA[A/C]TACCTACCCCTAGGG | 59349 |
rs775605295 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202918219 | CTCTCCTTGACTCAG[A/G]AGAATGAACTCTTCA | 59349 |
rs775642018 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202897111 | ATAATCATAAGGCTG[C/T]CGAATGGGGAGTTAT | 59349 |
rs775784323 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202903741 | GATTCTCCTGCCTCA[A/G]CCTCCCCAATAGCTG | 59349 |
rs775809741 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202898828 | TTCTGATTTGAACAA[A/C]ATAAGTACTCAAAAA | 59349 |
rs775820490 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202924681 | TCCAATAGCTGACAT[A/G]TGTGTTTTACTACAT | 59349 |
rs775908332 | snp | C/G/T | 3.29594e-05 | 0.00405941 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202896949 | CAACCACCAAAAGCA[C/G/T]TTCATTGGCTCCTGA | 59349 |
rs775920531 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202919022 | CTGGGAGGCAAGGTG[G/T]GAGGATCACTCGAGC | 59349 |
rs775935952 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202920061 | GCTCATGCCTGTAAT[A/C]CCAGCACTTTGAGAG | 59349 |
rs775945047 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202913749 | GCAGTTAGCCAGGGG[A/G]AGTAAGAGAGTACTC | 59349 |
rs776002316 | snp | C/T | 1.65658e-05 | 0.00287795 | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892502 | TGTCCACTGGACTGG[C/T]CACTAGCTCTGGATG | 59349 |
rs776170141 | snp | A/G | 3.30896e-05 | 0.00406739 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202919906 | TTTCCCCTTCTCTGA[A/G]AGCTGAAAATTCAAA | 59349 |
rs776206294 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202909053 | CATCTGACTCCGAAG[C/T]TCAGGCCTCAGATGA | 59349 |
rs776292447 | snp | A/C | 1.92158e-05 | 0.0030996 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925226 | CAAGAGGGAAAAAAA[A/C]ACAATGAGCATATTC | 59349 |
rs776342696 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202915161 | CTTATTTTATGCTCA[G/T]AACAGTCCTGTGTAC | 59349 |
rs776384124 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202918972 | AGAAAAACTGGGGAC[C/G]AGGAACGGTGGCTCG | 59349 |
rs776451336 | snp | C/T | 3.29489e-05 | 0.00405874 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202918321 | GGTTTCAGCAAAATC[C/T]CTAATACCCAGGCAA | 59349 |
rs776474146 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202905232 | AAGCAGGAGCCCCTT[C/G]TGCTGCCTGTTCAGA | 59349 |
rs776493002 | in-del | -/GA | 1.65239e-05 | 0.00287431 | intron-variant | KLHL12 | GRCh38.p7 | 1:202911034 | AAGGTTTTGGATCCT[-/GA]GAGTGTTGCACTACT | 59349 |
rs776573740 | snp | C/G | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891729 | AGTTATACTGAACTC[C/G]CACATTGATGTCATC | 59349 |
rs776692558 | snp | A/G | | | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929037 | TGTTTCGCCATCTTG[A/G]CCGGGCTGGTCTCGA | 59349 |
rs776692885 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202912964 | GGAAAGCGTAAAGCA[C/T]TCCAACAAAGGGTTT | 59349 |
rs776735315 | snp | A/G | 0.000328342 | 0.0128087 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893451 | TGAATGCATTAGCAA[A/G]TGTATGGTACTAAGC | 59349 |
rs776738981 | snp | C/T | 1.64866e-05 | 0.00287106 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202895573 | CATTCATAGGGGCCA[C/T]AGAATACCAGACCCC | 59349 |
rs776749632 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904798 | ATAACAGGGTTCAGA[C/G]ACTCACATTTCCATT | 59349 |
rs776876100 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202923208 | CATTTCCAAATAACA[A/G]AAGAGTAAAGACACT | 59349 |
rs776924763 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202925590 | AATGTCCTTAAGTAG[A/G]TAAGTATTTAGAGCA | 59349 |
rs776929159 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202898493 | TATTACTATGAGACA[C/T]TGAGTGCTTCCTAAT | 59349 |
rs776973483 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202923464 | ACCTGTCAGGTTCCT[A/G]TTTTCCCTACTAGCC | 59349 |
rs777074398 | snp | C/T | | | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202895641 | CTAAGGCGGGAACGG[C/T]CATCATAGCCACCAA | 59349 |
rs777110286 | snp | A/G | 1.64923e-05 | 0.00287156 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202919761 | TGTCTGTACCTTTCA[A/G]CTGAAGCAGACAGGC | 59349 |
rs777152960 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202917739 | AACATTTTTTTTGTC[C/T]ATATCTCTGTCTCTA | 59349 |
rs777162279 | snp | A/C | 1.65089e-05 | 0.00287301 | intron-variant | KLHL12 | GRCh38.p7 | 1:202896996 | AAGATGGGTTAGTTC[A/C]GCATCCCTGGATGGG | 59349 |
rs777234309 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202896484 | GTGTGAGCTACCACG[C/T]CCAGCCCAAACTTCT | 59349 |
rs777247548 | snp | C/G | 1.64765e-05 | 0.00287019 | missense, utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892602 | TGTCACGACTTCCCA[C/G]CTGTCGATGATAGGG | 59349 |
rs777294317 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202900651 | GGTGGATCACTTGAG[A/G]TCAGGAGTTCAAGGC | 59349 |
rs777434651 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202898075 | GATAAAATATTTCCT[A/G]CCTTGGCTTTTGGAG | 59349 |
rs777524779 | snp | A/C | 1.64795e-05 | 0.00287045 | missense | KLHL12 | GRCh38.p7 | 1:202894649 | TTCCCGGGCTGTCTG[A/C]ATATCTCCCAGCATG | 59349 |
rs777612953 | snp | C/G | 1.67142e-05 | 0.00289081 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918433 | AGAATAGTTGGACAG[C/G]TGTGATCTAGGATAT | 59349 |
rs777709619 | snp | C/T | 1.68709e-05 | 0.00290434 | intron-variant | KLHL12 | GRCh38.p7 | 1:202924922 | GTGAAATTAGACAAC[C/T]AGAGTTCCACGGGTT | 59349 |
rs777802372 | snp | A/G | 1.6516e-05 | 0.00287362 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908974 | GCAAGAAGTAGTTGA[A/G]AAGCATCCCCTCATT | 59349 |
rs777806542 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202920964 | TGTGGGTTATAACTC[C/T]AGTCTCTCCAGGACT | 59349 |
rs777812307 | snp | A/G | 1.64792e-05 | 0.00287042 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202893333 | TCCAGGAATCAGTGC[A/G]AATGTTGTATGCTTC | 59349 |
rs777998795 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202925552 | ATATAAAATTTCTTA[A/C]AGGTGTTATATTATT | 59349 |
rs778003702 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202915246 | TAACACATGCCACCC[A/G]GCCAAGACTAAATCC | 59349 |
rs778072680 | snp | C/T | 1.65655e-05 | 0.00287793 | intron-variant | KLHL12 | GRCh38.p7 | 1:202909149 | AGCAGACAGCAGAGT[C/T]AGGCACTGGGGATAC | 59349 |
rs778107107 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202910884 | CTTGCCAAGAAATTC[A/G]CTTTTCTTAGAAATA | 59349 |
rs778115101 | in-del | -/A | 8.87863e-05 | 0.00666223 | intron-variant | KLHL12 | GRCh38.p7 | 1:202894291 | ATCCTCCTGGAAGAC[-/A]AGAGACCATTCCAGA | 59349 |
rs778192190 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911607 | GGGAATCTGTTGCCT[C/T]ATTCGAAGTCAGCTC | 59349 |
rs778204864 | in-del | -/C | 1.93183e-05 | 0.00310785 | intron-variant | KLHL12 | GRCh38.p7 | 1:202925228 | AGAGGGAAAAAAAAA[-/C]AATGAGCATATTCAA | 59349 |
rs778314462 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202920753 | GGTAGTTATCTATAC[A/G]CCAGGAATAAGTAAT | 59349 |
rs778392292 | snp | C/T | | | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202925043 | AGGGAAGTCTTTCTG[C/T]TCTACTCTCAATGTC | 59349 |
rs778398014 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202924380 | TTGTTAGGAGGAGTG[C/G]GATGTGGTTTGAATC | 59349 |
rs778473697 | snp | C/T | 8.87823e-05 | 0.00666208 | missense | KLHL12 | GRCh38.p7 | 1:202894229 | TAGTCCAATGTCCTG[C/T]ATGAGGGTCGTATTT | 59349 |
rs778475908 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202896387 | GTAGAGACAGAGTCT[C/T]ACCATATTGCCCAGG | 59349 |
rs778489326 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202924171 | AGGCAATTACTAAGT[A/G]GTGTTTCTTAATACT | 59349 |
rs778553825 | snp | C/T | 6.639e-05 | 0.00576113 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918417 | AGGCAGCAAACACTT[C/T]AGAATAGTTGGACAG | 59349 |
rs778559836 | snp | A/T | 1.64738e-05 | 0.00286995 | missense | KLHL12 | GRCh38.p7 | 1:202918287 | CCTCAGCTGCTTGCA[A/T]CAGGTCAACACAATT | 59349 |
rs778670064 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202910801 | TATATAAAACACTCA[C/G]AGGCATGTAAAACAG | 59349 |
rs778671020 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904997 | AGTCATTATCCTGGT[A/G]GCTGGTTTAGCAGCC | 59349 |
rs778779595 | snp | C/T | 1.64727e-05 | 0.00286986 | stop-gained, intron-variant | KLHL12 | GRCh38.p7 | 1:202896867 | ACTGGCAAAAAGCTC[C/T]ACTCCTGAGTCTTGG | 59349 |
rs778869552 | snp | G/T | 3.37405e-05 | 0.0041072 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202895711 | AACGTCTCTTACGAG[G/T]GATGCTCTATGGATT | 59349 |
rs778930553 | snp | C/T | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891743 | CCCACATTGATGTCA[C/T]CTTCTCTCATCCCAA | 59349 |
rs778944471 | in-del | -/AAAAAAAAAAA | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202899823 | GTAAGACTCCATCTC[-/AAAAAAAAAAA]AAAAAAATAATAATA | 59349 |
rs778958066 | snp | G/T | 8.23649e-05 | 0.00641683 | missense | KLHL12 | GRCh38.p7 | 1:202925031 | AATCCGATGGGCAGG[G/T]AAGTCTTTCTGCTCT | 59349 |
rs779038985 | snp | C/T | | | missense | KLHL12 | GRCh38.p7 | 1:202892651 | CTTAGCAGGGAATTA[C/T]CATCATATCTGAGTG | 59349 |
rs779102949 | snp | C/T | 0.00016503 | 0.00908228 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908980 | AGTAGTTGAAAAGCA[C/T]CCCCTCATTCTGCCG | 59349 |
rs779133215 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202915075 | CATTAATGCCTCACT[A/T]CAGAGAAAAATAGAT | 59349 |
rs779157649 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926950 | CCAGATGCCCCACCC[C/T]ACTGCCAGCCTTCCT | 59349 |
rs779252034 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202923098 | CTCTCCTTTGAACAA[G/T]TACTCTCAAAAATAA | 59349 |
rs779349411 | in-del | -/TC | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911457 | ATATATATATATGTA[-/TC]TCTCTCTCTCTCTCT | 59349 |
rs779604147 | snp | C/T | 6.64717e-05 | 0.00576467 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918166 | ACATCAAGACAAATC[C/T]GTACCTGAATTTCGT | 59349 |
rs779717291 | in-del | -/AGT | 1.64772e-05 | 0.00287025 | cds-indel | KLHL12 | GRCh38.p7 | 1:202894597 | ACTCAATACCTAGAC[-/AGT]AGATCACTCCACTGG | 59349 |
rs779795387 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202910560 | CACAGGTGGTATATA[C/T]GGTAAAAATTATGAA | 59349 |
rs779928725 | snp | A/C/T | 5.01948e-05 | 0.00500952 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919952 | ATGGTTATAATTCCA[A/C/T]AAGATAAAGGCAGAA | 59349 |
rs779986934 | in-del | -/TA | | | frameshift-variant | KLHL12 | GRCh38.p7 | 1:202909109 | CCCTGCATTGTAAAC[-/TA]CAGCGGATGAAAGGC | 59349 |
rs780003210 | snp | A/G | 1.6666e-05 | 0.00288664 | synonymous-codon, intron-variant | KLHL12 | GRCh38.p7 | 1:202895529 | CAGCCTACCTCCCAG[A/G]GTGGTGGCTCCAGCA | 59349 |
rs780065495 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202917862 | ATTCTCAATAAATGT[C/T]TGTGAAATGAGTGAA | 59349 |
rs780081659 | snp | C/G | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892449 | GCACATAGTGAGAAA[C/G]AGACATTCTGGAAAG | 59349 |
rs780168678 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202896268 | CACAGTTCACTGCAA[C/T]CTCGAACTCCTGGGC | 59349 |
rs780265307 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202901755 | GTAATTAACTTCCCC[A/G]CAACTGCCAACAGAG | 59349 |
rs780282596 | snp | A/G | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202891513 | AAAGAATGGGGCAGT[A/G]ATCAGGTAGCTGAAC | 59349 |
rs780295621 | snp | C/T | 1.64925e-05 | 0.00287158 | missense | KLHL12 | GRCh38.p7 | 1:202909111 | CTGCATTGTAAACTA[C/T]AGCGGATGAAAGGCT | 59349 |
rs780385504 | snp | C/T | 6.59554e-05 | 0.00574224 | intron-variant | KLHL12 | GRCh38.p7 | 1:202908994 | ATCCCCTCATTCTGC[C/T]GAGATACCAGCTTAC | 59349 |
rs780477366 | snp | C/G | 8.25962e-05 | 0.00642583 | missense, utr-variant-5-prime | KLHL12 | GRCh38.p7 | 1:202925176 | ATAAAGCAGTGCGGA[C/G]AAAGAACAAAATGGG | 59349 |
rs780477477 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926003 | CTAGCTACCAAGAAG[C/G]CTGAGGCCCGAGAAT | 59349 |
rs780489091 | snp | C/T | 9.13784e-05 | 0.00675876 | missense | KLHL12 | GRCh38.p7 | 1:202894202 | AACGCTTGGTGGCCA[C/T]TGGTGTAACATTAGT | 59349 |
rs780563439 | snp | A/G | 1.64732e-05 | 0.0028699 | missense | KLHL12 | GRCh38.p7 | 1:202925069 | ATGTCACATCACAGA[A/G]GGTATTGCTCTTCCT | 59349 |
rs780577037 | snp | C/G | 1.64808e-05 | 0.00287057 | synonymous-codon, intron-variant | KLHL12 | GRCh38.p7 | 1:202893352 | GTTGTATGCTTCAAC[C/G]GAAGAAAGGTGGGCT | 59349 |
rs780751635 | snp | C/T | 1.71187e-05 | 0.00292559 | intron-variant | KLHL12 | GRCh38.p7 | 1:202895504 | GATGGAAATAATTGC[C/T]CTGCACATCCAGCCT | 59349 |
rs780850589 | snp | A/C | 3.2969e-05 | 0.00405998 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202895645 | GGCGGGAACGGCCAT[A/C]ATAGCCACCAATGAC | 59349 |
rs780957461 | in-del | -/AA | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202914865 | AGCGAAACTCCGTCT[-/AA]AAAAAAAAAAAAAAA | 59349 |
rs780973829 | snp | C/G | | | upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202929339 | ACATATACTCGTGCA[C/G]ATGTAAAACGATGTA | 59349 |
rs781026393 | snp | C/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202894410 | TTCCAATAACTCTAA[C/G]AGAAATCTGACATTA | 59349 |
rs781041653 | snp | C/G | 1.67365e-05 | 0.00289275 | intron-variant | KLHL12 | GRCh38.p7 | 1:202919704 | ACTATTAATTTTCAA[C/G]CTTTCCAGGGCTATT | 59349 |
rs781048770 | snp | A/C | | | utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892043 | AATGGAACTGTGTTG[A/C]CCCTAGCTACCTGTA | 59349 |
rs781115585 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon, intron-variant | KLHL12 | GRCh38.p7 | 1:202896905 | TTTCTCTACCACATC[A/G]ATGGGAGACTGCTGG | 59349 |
rs781125368 | snp | C/T | 1.64988e-05 | 0.00287213 | missense | KLHL12 | GRCh38.p7 | 1:202894689 | TCAATGTTTGGATCA[C/T]AGCGCTCCATACTGG | 59349 |
rs781202014 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon | KLHL12 | GRCh38.p7 | 1:202925055 | CTGCTCTACTCTCAA[C/T]GTCACATCACAGAGG | 59349 |
rs781206995 | in-del | -/A | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911411 | AGTCAATTTGGGTTA[-/A]AAAAAAAAATATATA | 59349 |
rs781223963 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202922778 | GGCGTGAGCCACCAC[A/G]CCCAGCTGAAGATCC | 59349 |
rs781225987 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202907930 | AAAAATAAAATATAG[C/T]GGATAAATCACCATT | 59349 |
rs781255625 | snp | A/G | 1.6489e-05 | 0.00287128 | missense, utr-variant-3-prime | KLHL12 | GRCh38.p7 | 1:202892544 | ATGGTCACTTCTCGC[A/G]GAGAACACAAACACC | 59349 |
rs781308655 | snp | G/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202904946 | GGCTATTTTAACTTG[G/T]CTGTCAATTTAATTT | 59349 |
rs781317380 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202909141 | TGAAATATAGCAGAC[A/G]GCAGAGTTAGGCACT | 59349 |
rs781405149 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202913552 | TCAGATATGATCCTT[A/G]CTCTTAAATGGGGAG | 59349 |
rs781424433 | snp | A/C | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202903736 | AAAATGATTCTCCTG[A/C]CTCAACCTCCCCAAT | 59349 |
rs781512383 | in-del | -/A | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202898977 | TAGAGACACACGTGG[-/A]AGTATGACACATAGG | 59349 |
rs781515333 | snp | C/T | 3.58539e-05 | 0.00423387 | intron-variant | KLHL12 | GRCh38.p7 | 1:202893209 | TGCTCTGGCTACATA[C/T]TGAGTCTGGATTCGT | 59349 |
rs781595002 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202926680 | TCCTGCCTCAACACT[C/T]CAAGTCTCAGCATAT | 59349 |
rs781610552 | in-del | -/TA | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202907623 | AAAAAGGAAAAAAAT[-/TA]TATATATATATATAT | 59349 |
rs781627618 | snp | A/C | 1.64803e-05 | 0.00287052 | missense, intron-variant | KLHL12 | GRCh38.p7 | 1:202893345 | TGCGAATGTTGTATG[A/C]TTCAACGGAAGAAAG | 59349 |
rs781637499 | snp | A/T | 1.68046e-05 | 0.00289862 | intron-variant | KLHL12 | GRCh38.p7 | 1:202918149 | ATCTTGAAGAAACCA[A/T]AACATCAAGACAAAT | 59349 |
rs781663525 | snp | C/G | | | intron-variant, upstream-variant-2KB | KLHL12 | GRCh38.p7 | 1:202927397 | ATTACAAAAAGGTCG[C/G]GTGGGCAGGGAATGG | 59349 |
rs781698548 | snp | C/T | 3.29571e-05 | 0.00405924 | missense | KLHL12 | GRCh38.p7 | 1:202911139 | GGCAAGGATTCTTCC[C/T]GCTCTTTCTTGGCAT | 59349 |
rs781703249 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202903416 | TTACTTGCCCTTCTG[C/T]GAACTGTACACTCAA | 59349 |
rs781775545 | in-del | -/A | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202921708 | TTTAGCTAAGAGAAG[-/A]AATCTTCAATTTTAC | 59349 |
rs796080255 | in-del | -/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202912988 | GGGTTTTAATGCAGA[-/T]TTTTTTTTTTTTTGG | 59349 |
rs796191275 | in-del | -/A | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202899837 | CAAAAAAAAAAAAAA[-/A]AAATAATAATAATAA | 59349 |
rs796211024 | in-del | -/CTCT | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911476 | TCTCTCTCTCTCTCT[-/CTCT]AAGATAGATAGTACC | 59349 |
rs796372930 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202911046 | CCTGAGAGTGTTGCA[C/T]TACTTACCTCAGCAT | 59349 |
rs796522776 | snp | C/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202913228 | ACACTCTAAAAAAAC[C/T]TACACTACATCACTG | 59349 |
rs796569809 | in-del | -/A | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202899840 | AAAAAAAAAAAAAAA[-/A]TAATAATAATAAATA | 59349 |
rs796588127 | snp | A/G | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202917184 | ATGCCTGCCTGGCAC[A/G]GGTAGTATCCCCCTG | 59349 |
rs796591734 | snp | A/T | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202899844 | AAAAAAAAAAAATAA[A/T]AATAATAAATAAAAA | 59349 |
rs796713342 | in-del | -/AAA | | | intron-variant | KLHL12 | GRCh38.p7 | 1:202923872 | AACTAAAAAAAAAAC[-/AAA]AAACAAACAAAAAAC | 59349 |