SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs147447049 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214829 | TTTGCTGAAATAGAT[G/T]TAGTCCTCTAGAGTG | 56916 |
rs147470134 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267102 | TTTCTCACATGTTCA[C/G]AATACAATATATTTA | 56916 |
rs147470149 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212467 | GGCATGAGCCACCAC[A/G]CCCAGCCCTATACAT | 56916 |
rs147479801 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261229 | TTAGTATAATCTAAC[A/G]TTGGTTTTCTTAATA | 56916 |
rs147595404 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279669 | CATTTTGCCTACAAA[A/G]CCTAAAATATGATCT | 56916 |
rs147616284 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207201 | TTTGAAGCTCAGCAT[C/T]CCGGGGTTCTTATCC | 56916 |
rs147809831 | in-del | -/T | 0.16028 | 0.233346 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224592 | TCAGATTTTAGAACA[-/T]TTTTTATTTTGGGTT | 56916 |
rs147817385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257538 | TAACATGGTGGCAGT[A/G]GAGTGTTCTTACATC | 56916 |
rs147826928 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250483 | AATTGAGAAAACATT[A/T]CTTGATCCTCTAGTG | 56916 |
rs147900062 | snp | A/G | 0.00835141 | 0.0640778 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206179 | CAGTGTATCGAAATG[A/G]TATCTGCATTCTCAT | 56916 |
rs147933685 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275732 | GCAGATTACTTACAA[A/G]TTATACCCAAATTGA | 56916 |
rs147946963 | in-del | -/A | 0.16028 | 0.233346 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225299 | CTTTCCTTGGCTTGT[-/A]AAGGTGATCTCCTTC | 56916 |
rs147986164 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247419 | CAGAGCTGGCATAAG[C/T]GTGGGACCCAAGAGC | 56916 |
rs148102079 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267121 | ACAATATATTTAATC[A/G]AGTGTGTCTTGCCTT | 56916 |
rs148251465 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286936 | GAGGCGCAATCTCCG[C/T]GCACTGCAAGCTCCG | 56916 |
rs148312628 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220513 | TCGGCCTCCCAAAGT[A/G]CTGGGATTACAGGCA | 56916 |
rs148322335 | snp | A/G | 1.65578e-05 | 0.00287726 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94250805 | CACAGAAGCTTTAGA[A/G]TCTCTAAAAGTGTTT | 56916 |
rs148335361 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272978 | ATGCCTGGCTAATTT[C/T]GTATTTTTGTAGAGA | 56916 |
rs148376545 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214555 | ACAGGCATGAGCCAC[C/T]GCACCTGGCCAAGCG | 56916 |
rs148440243 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237568 | AGTGAAAGCAAACCC[A/T]CACTTCATTAACCAC | 56916 |
rs148470934 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216198 | CTCTGCCCCCATCAC[C/G]TAATACCCCTTCCTC | 56916 |
rs148492012 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232009 | TGGGATTACAGGCAC[C/T]CGCCACCATGCCAAG | 56916 |
rs148502198 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249506 | GACATAAATATGTCA[A/G]TGTTCACAGAAACAA | 56916 |
rs148566409 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242885 | TATGCCACTGCACTC[C/T]AGCCTGGGTGACACA | 56916 |
rs148680809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262033 | AAATGCTTCTAAATG[C/T]TGGTGTTCTTCAAGG | 56916 |
rs148701911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94279109 | TTAAGTTGTTAGGCT[A/G]TAAGATTGGTGAACC | 56916 |
rs148723204 | snp | G/T | 0.0150606 | 0.0854603 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94205867 | CAATGGCGTGATCTC[G/T]GCTCACTGCAAGCTC | 56916 |
rs148764672 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288145 | GGCAATTTATTTTCA[A/G]TATCACAGCATATTC | 56916 |
rs148840372 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222782 | AGCCTGGCAAACATG[A/G]TGAAACCCAGTCTCT | 56916 |
rs148851766 | snp | C/G | 4.94393e-05 | 0.00497164 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94274789 | CTTTGAAGGTCCTCT[C/G]TTACTATGGTAAGAA | 56916 |
rs148873580 | snp | C/T | 0.00146481 | 0.0270233 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289742 | AAGAAGCCACAAATA[C/T]GTAGTTCTGAAGATG | 56916 |
rs148978554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259249 | TTAATTTTGGAAGCA[A/G]CATACCAAATCTGAA | 56916 |
rs149019191 | snp | A/G | 0.00125624 | 0.0250308 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94233997 | CAAGGCCTTCCTACC[A/G]TGGCACGTAGAAATG | 56916 |
rs149181063 | in-del | -/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244862 | TTTTGCCTCCAAAAA[-/C]CCACCTCTCTGATAA | 56916 |
rs149211090 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265334 | AAATAAAATGAAATG[A/C]TATCCCATACTGTGA | 56916 |
rs149218979 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280168 | CTGCACCTGACCAAC[C/T]CATTTCTTTTTAAAT | 56916 |
rs149317146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231129 | GATGTAGAAAATCAG[C/T]CTAATAAAATCTGTG | 56916 |
rs149327330 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283410 | TTTTTGTTTTTTCGG[C/G]AAAGCATGGCTACTG | 56916 |
rs149348769 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212466 | AGGCATGAGCCACCA[C/T]GCCCAGCCCTATACA | 56916 |
rs149369347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223935 | TTGTTAAAGTGTTCA[A/G]TTGACAGGCATTAGC | 56916 |
rs149382511 | snp | A/G | 8.27808e-05 | 0.006433 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94278678 | AATGTCGGAGAAGCA[A/G]GAGCAACTCTATTTG | 56916 |
rs149465538 | in-del | -/TTG | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247119 | GTAGTAATTGCTTAT[-/TTG]TGTTTTGATTGAGAG | 56916 |
rs149486572 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242442 | TTCTTTTTAGCCTCT[G/T]TTCCTGATACATTGC | 56916 |
rs149538841 | snp | C/T | 0.00218077 | 0.0329489 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236941 | ACATTAATCTTTTCT[C/T]GTTCTGTTAGTTGAT | 56916 |
rs149562017 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256465 | CCTCCCGGGTTCAAG[C/G]GATTCTCCTGCCTCA | 56916 |
rs149569518 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272452 | GACTTTTTACATATA[A/T]GTACACCCATGTGAC | 56916 |
rs149610662 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214354 | TGCAATCTCTGCTCT[C/T]GGGTTCATGCCATTC | 56916 |
rs149664266 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282119 | TTTTTTTTTTTTTTG[A/T]GACGGAGTCTCGCTC | 56916 |
rs149676050 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275195 | ATAAAAAGGTTTTGC[C/T]TAGTTATTGAAAAAA | 56916 |
rs149689941 | in-del | -/A | 0.163236 | 0.234461 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206312 | TATTATTTCGCCATT[-/A]AAAAAAAATGAGATC | 56916 |
rs149718391 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215511 | CTGTAGTCCTAGCCA[C/G]TTGGGAGGTTGAGAC | 56916 |
rs149764998 | in-del | -/T | 0.135484 | 0.22223 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277383 | TCTTGGTTAATATCC[-/T]TAATTTTCTGAAGGA | 56916 |
rs149834409 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233585 | ATTTAATCTTCATAA[C/T]TTCTTAGGAGTAGCA | 56916 |
rs149886901 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226907 | TGGGGTCTTGCTATG[C/T]TGTCCAGGCTGCTCT | 56916 |
rs149930847 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261487 | TTATGAATAAAATTA[G/T]ACATTTATAACCACT | 56916 |
rs149995569 | in-del | -/A | 0.0197687 | 0.0974348 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234582 | GAGAAATATTGATTT[-/A]AACTACAGAAACAAA | 56916 |
rs150015332 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244535 | TTAAGGCTCCTAAAG[A/G]TAACATAACTGTGAT | 56916 |
rs150076406 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258540 | GGCCTTAGCATTTCA[A/T]TTTCCTGTCATCCTG | 56916 |
rs150108998 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248045 | TGTTGTTCTCATTTT[A/T]ATGAACACGTGTACC | 56916 |
rs150153569 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282806 | ATATACTTCTGAGAA[C/G]GTTAAAGATTGAAAA | 56916 |
rs150166232 | in-del | -/TACT | 0.00398564 | 0.0444627 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266407 | ATTTTTTAAATGAAA[-/TACT]TAATAGATGAGAAAA | 56916 |
rs150172157 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207800 | ATGCCTTAGCATGCA[C/T]TCCACCTCTGAACCT | 56916 |
rs150182435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223640 | GTGGCACGATCCTGG[C/T]TCACTGCAGTCTCTG | 56916 |
rs150204964 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276643 | AAATATTTCACACTT[C/T]ATGGACTAGATGGCC | 56916 |
rs150233850 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218310 | TTTTTTTGAGATAGA[A/G]TGTCACTCTGTCCCC | 56916 |
rs150247319 | snp | A/G | 3.29478e-05 | 0.00405867 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94277084 | GTTAGAACTCATGTC[A/G]CTGTTGAATTTTGTT | 56916 |
rs150300117 | snp | A/G | 1.6476e-05 | 0.00287014 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208538 | GAATGCTGAAGGGGA[A/G]GTTAGCAGGGCAAAC | 56916 |
rs150361873 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235960 | ACACTCCAGAGCACT[C/G]TCTTGAAGTAATCTC | 56916 |
rs150371440 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287189 | TGTGTTTTTCCCAGT[A/G]TGTATTTTATTTGCT | 56916 |
rs150382676 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250962 | CAAAAGATGTTGAAA[C/G]TAATGATGTAAAAAC | 56916 |
rs150413551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229744 | ACCTAGGAAATACTC[A/G]GGTGTAGGGGGTTGG | 56916 |
rs150445190 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265079 | TTTCATTGATTTCCC[C/T]CACCCCCAAGTAGGG | 56916 |
rs150554386 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267402 | TTTTGGTCGGACAGC[A/G]TCCGTAACCTGTTTT | 56916 |
rs150622661 | in-del | -/TGGCAA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247705 | CCTCCCCCTAACCCC[-/TGGCAA]CCGCCAATCTGCCTT | 56916 |
rs150669304 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284833 | CTCAAGTGGCTTAAA[G/T]AAAAGAATTTAAGGA | 56916 |
rs150687355 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212148 | ATGAGTGGGCATTAT[G/T]AGTACTTTATACATT | 56916 |
rs150720338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94279182 | TTTTTTTTTTCAGAC[C/T]AGGTCTGGTTCTGTT | 56916 |
rs150762185 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221153 | AAACTAGTGTCCATG[A/C]CTGTGAGTTTGACAG | 56916 |
rs150777961 | snp | A/G | 8.25825e-05 | 0.0064253 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94283299 | CATAGAGTAGGCCAG[A/G]CTAAGTAAGTGTTTT | 56916 |
rs150825146 | snp | C/G | 0.000178835 | 0.00945439 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252697 | ACCCTAAAAATGCAA[C/G]TAAAACAAAACTAAA | 56916 |
rs150878933 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238168 | TCTACATAAGATTTT[A/T]ATTTTATCCATATGA | 56916 |
rs150900549 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255582 | TATAAAATGTAAGTA[A/T]AATATACTTATTAAT | 56916 |
rs150964570 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222896 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGGGAGC | 56916 |
rs151008293 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257795 | TCCATATCTTTATGT[A/C]ATATAGTTATAATGC | 56916 |
rs151060434 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250215 | AAAAGACTCATGCCA[C/T]GCATCCTGTTGCTAA | 56916 |
rs151125076 | snp | C/T | 0.00178678 | 0.0298361 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94276457 | TCCATTCGCTACCAG[C/T]ACCTTATGACAATTA | 56916 |
rs151159818 | in-del | -/AG | 0.0146672 | 0.084371 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261076 | TATGCTAATTTTTTC[-/AG]AGTTACCTCTCGTGT | 56916 |
rs151166936 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217873 | AATAGAAAATTATCA[A/C]AGTGTATTGCTTATA | 56916 |
rs151177090 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269620 | GATGTTCAATAAGTG[A/G]TAACTGTTAATAGTT | 56916 |
rs151219555 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213208 | CCATATAATAGGGCA[A/G]AATACTAAGCAAAGT | 56916 |
rs151249837 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244271 | TGCTAGTAGTGGTTG[C/T]TTTAATGATTTCAAA | 56916 |
rs151252151 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281295 | TCATATATAGGCTGC[A/T]ATAAGACATACGTCT | 56916 |
rs151265873 | in-del | -/AAG | 0.495016 | 0.0496707 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262913 | AAAAAAAAAGAAAGA[-/AAG]AAAGAAATGGTAGTT | 56916 |
rs151319898 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239579 | TTTTTTTTTTTTTTA[A/T]TTTTTTATTTTGAGA | 56916 |
rs151333681 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228577 | ATTTATAAATAAGGA[A/G]TATGTCTTAGAATGC | 56916 |
rs180739184 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289964 | TGTTTTTGCTTGTCT[C/T]ATTTGAAGTTCTTTT | 56916 |
rs180753952 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272039 | GGTGGACAGTCCAAG[A/T]TGAGTGTATCGGTAG | 56916 |
rs180768162 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225264 | CAAGATCAAGTTGGC[A/C]TGTGTTTTCTTCTTG | 56916 |
rs180771561 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250693 | TAAAAGAGCATAGAC[A/G]TTTTCTGCAAGTTGC | 56916 |
rs180772290 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279679 | ACAAAGCCTAAAATA[C/T]GATCTGGCCCTTTAC | 56916 |
rs180775186 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259418 | CTGCTGTTTTACATT[C/T]GTGGTTAGTGGATTG | 56916 |
rs180781494 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207984 | TTCTCGAGGCAGGGG[A/G]CACGGTAGCACAGGG | 56916 |
rs180815840 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243011 | AGAGTCTCATCCTGT[A/C]GCCCAGGCATGATCT | 56916 |
rs180904678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221418 | TCTAAGAAATTACCA[C/T]CTGTCAAGTTTGGGT | 56916 |
rs180916824 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254276 | AAAGTATTTGCTGAA[A/G]GGCTTTCTTGTTCTT | 56916 |
rs180943595 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237418 | ATACAAAAATAAATG[C/T]ATTTGAATGAGCTTG | 56916 |
rs181091774 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225086 | AAATAATGTTGGAAT[C/T]TACCCCTTGGAGAGA | 56916 |
rs181097981 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207542 | TACCATGACAACAGC[G/T]CGCGCCTCGACATTG | 56916 |
rs181407895 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249390 | TCTAGTTTTTTAGGA[A/G]ATTTATCTCATTTTA | 56916 |
rs181425649 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233009 | CACACATATTCTGTT[C/G]TTTGGAAATTTGCTT | 56916 |
rs181431486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217098 | CAACCTTGTTATTTC[C/T]TGTGTTTTTGATAAT | 56916 |
rs181456210 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242143 | GGTTCAAGCAATTCT[C/T]GCACCTCAGCCTCCG | 56916 |
rs181521451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275135 | TTGGTGTGTAATACC[C/T]ATATAGGAGGTTTTT | 56916 |
rs181537086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94253433 | TAGCAACGGCCAGGG[A/G]AGCTCCATGATTCAA | 56916 |
rs181544772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236591 | CACACATACACAAAC[A/G]TGAGCATGCACACAC | 56916 |
rs181544894 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220391 | TAGCTGGGACTACAG[G/T]CGTGTGCCACCACAC | 56916 |
rs181564356 | snp | A/G | 3.29728e-05 | 0.00406021 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289538 | ATGGGCCTGTGAAAT[A/G]AGAACTGTGAACTCT | 56916 |
rs181567145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280120 | TTTACCCACCTCGGC[C/T]TCCCAAAGTGCTGGG | 56916 |
rs181567860 | snp | C/T | 0.000578001 | 0.0169902 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94264799 | TGTAGTTATAAGGCT[C/T]ATGAACAAATGTGAA | 56916 |
rs181570366 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243860 | ATTCAACATCTCAAA[A/C]CTACCTAAGCATTCT | 56916 |
rs181574127 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259986 | AGTAAGGTCCACTTA[A/T]TAAGATTGCTTGATA | 56916 |
rs181582274 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225569 | TATTGGTGATTGGGA[C/T]TTAATGATGGGGAGG | 56916 |
rs181585117 | snp | A/G | 0.000172965 | 0.009298 | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208223 | CAATGAAGCGCAGCC[A/G]TAACAGTCCTGAGCC | 56916 |
rs181640675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229089 | TATTGTTGAACTTTG[A/G]TGACTCAATTAACGT | 56916 |
rs181670598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284544 | CTAGGATTACAGGTG[C/T]GTGCCACCACACCCA | 56916 |
rs181721472 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246603 | CTACACTCCCACGAA[A/C]GTGGTGGGCCTCAGA | 56916 |
rs181724689 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212452 | AGTGCTAGGATTATA[C/G]GCATGAGCCACCACG | 56916 |
rs181747220 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288639 | TAGATTATAGCTGAG[C/G]TGTATATTTGTGAGA | 56916 |
rs181754684 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212809 | TAGGACCTTAAAATA[G/T]TCCCTTTAGCCATCA | 56916 |
rs181784668 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248821 | TCAGAATTTAGTTAT[G/T]TCTATCTAAGGTACT | 56916 |
rs181788555 | snp | C/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216654 | GGCAACTACCGTTTA[C/T]GTTGTCTTTTTATGA | 56916 |
rs182013143 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94263710 | ATGTGATTCTTGTCA[G/T]AACTTGGAAAAATAT | 56916 |
rs182016970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269912 | TCCTGAGCTCAAGCA[A/G]TCTGCCCAGCACAGC | 56916 |
rs182019520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284158 | AACCCCGTCTCTACT[A/G]AAAATACAAAAAAAA | 56916 |
rs182022552 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246272 | TTACAGGTGCCTGCC[A/G]CCACGCCTGGCTAAT | 56916 |
rs182028047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232570 | ATTTGAAGGACAGGC[A/G]TAGTGATAAAGGAAG | 56916 |
rs182039178 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228741 | ACAGTTGGAGAACTA[A/G]CAGTCAGTCCCTGGA | 56916 |
rs182160942 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245208 | GGATATTGAGAAGTT[C/T]CTAGGGTCCTGTCCT | 56916 |
rs182162526 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226865 | CAGGGAATCGTTTCT[C/T]TTTTTTTTTCTTGTT | 56916 |
rs182255089 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276044 | CCTCGTGATCCGCCC[G/T]CCTCGGCCTCCAAAA | 56916 |
rs182313054 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246746 | GATCAAGTGATACTC[C/T]CTAGACTGTGCAAAA | 56916 |
rs182313664 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238626 | TCAAAAGAAAGAAAG[A/G]AAGAAAGAAAGAAAA | 56916 |
rs182316084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265660 | TAAGTAGTTTGGAGA[C/T]TCAGAACTGTTCAGA | 56916 |
rs182320485 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229409 | TGAAATTATAGATGT[A/G]TACTTATTCAGTGGT | 56916 |
rs182333094 | snp | C/T | 0.000473709 | 0.0153828 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213162 | AAAATGGTATGTAAA[C/T]ATATAGTTAAAATAG | 56916 |
rs182445106 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261030 | AGCTGTTCAGTGGCA[A/G]AAAATATGATAATGA | 56916 |
rs182462005 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233554 | TAGGCCTGAAAATTA[C/G]TTTATCTTTGTATCC | 56916 |
rs182548754 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254851 | ATTTGCTTAGAACTT[A/T]GAGCTCCTACTTTAA | 56916 |
rs182582601 | snp | A/C | 0.0202668 | 0.0986035 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285113 | TATTTATCTATATGA[A/C]CATGCATCTAATTAG | 56916 |
rs182584930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222111 | ACGGAGAGGGTACCC[C/T]TCCCAGAGGAGCCTT | 56916 |
rs182588562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223480 | CCTGGGCGACAGAGC[A/G]AGACTCTGTCTCAAA | 56916 |
rs182632302 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273506 | TTAGAGTTGCATTCT[C/G]GGAAATCAAAAGTGA | 56916 |
rs182641818 | snp | A/T | 0.000525256 | 0.0161973 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290782 | TGTTTTGTTTTTATT[A/T]TGTAAATATCATTAT | 56916 |
rs182642926 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252098 | CTTGTGATCTGCCCG[C/T]GTCGGCCTCCCAAAG | 56916 |
rs182657337 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218461 | CGACGCCCAGCTAAT[A/G]TTTGTATTTTTGGTG | 56916 |
rs182660070 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235106 | CACCCATTTAAAATA[C/T]ACAATTTTGTGGTTT | 56916 |
rs182663931 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281262 | CTAGCTTTTAGCCCT[C/G]AAGTTAAGGCAGTTT | 56916 |
rs182740925 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217811 | AAAATCAATTTCTTG[A/G]GTCCTGACTAAATAT | 56916 |
rs182768487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276243 | CTGGCTGTTAGAAAT[A/G]TGTAAATAAAAAATG | 56916 |
rs182783288 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255245 | TGAAATCATTGTTTA[A/T]TCTTACTTAGTCTTA | 56916 |
rs182791116 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239396 | ACAGTATCATCCTGC[A/G]TATTAAACACTAGGG | 56916 |
rs182792689 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222721 | TAATCCCAACATTTC[A/G]GGAGGCCGAGGCAGG | 56916 |
rs182798844 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94205757 | GCTCTGCCTTGGCCT[C/T]CCAAAGTGCTGGGAT | 56916 |
rs182852945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239792 | TGCCAAGGCTGATCT[C/T]GAACTCCTGAGCCCC | 56916 |
rs182989057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255600 | TATACTTATTAATAT[C/T]ACCTACTTGGTAATC | 56916 |
rs183040671 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227638 | GAGTTACTAGGTACT[A/C/G]AGATAAAGGTGACTG | 56916 |
rs183155110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280930 | TTTCTTGACGTATTT[C/T]CTTGATTACCTCCTT | 56916 |
rs183172836 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244218 | TACACAGACCTAAAA[C/T]AGAAGTCACTGTACC | 56916 |
rs183197611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209225 | AACTATTAGAGGAAT[A/G]TATTTGAGCTCTTGT | 56916 |
rs183276797 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276911 | GAATGTTAAATTATT[A/G]ATAATGGTTTTAATT | 56916 |
rs183298381 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267877 | TAGAAAACTGTGAAG[C/T]GTCAAAATAGATGGG | 56916 |
rs183301524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231049 | TTGTCCTTAGTGAGA[A/G]CAGTTTCACTGAGTT | 56916 |
rs183350485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261766 | AGGCACGTGCCACCA[C/T]ACCGGCTAATTTTTT | 56916 |
rs183354523 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282023 | GTAGCCTGGGTGACA[C/G]AGCGGGACCCTATCT | 56916 |
rs183361550 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245512 | ACCACAGAAATTTTA[C/T]TTATTCTTTATATTT | 56916 |
rs183407029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260375 | TTGAGACAGTCTCTC[A/G]CTCTGTCACTCAGGC | 56916 |
rs183431978 | snp | C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226295 | GATACAGTGATTATA[C/G]TGTAAGCTGATTAAT | 56916 |
rs183432903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94251709 | TGAATAAAGTATTGT[A/G]TTATAGATTGGTGCA | 56916 |
rs183458788 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218049 | TGCTCTTGCTTTATT[A/C]AGAGCATAGAGAAAA | 56916 |
rs183480407 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291381 | CACAAATGAGATTAT[C/T]TTATGTGCTTAATAT | 56916 |
rs183481415 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246141 | TTTTTTTCTTTTGAG[A/G]TGGAGTCTCGCACTG | 56916 |
rs183482744 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262824 | GTGTTTCCCAATGTT[C/T]GTAGACCACAAGGAC | 56916 |
rs183492703 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273867 | CTTTATACTTTTCTC[C/G]TTTGTTTATATATGT | 56916 |
rs183495491 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228610 | ATCAGGGTACTGATT[C/G]CTTCACCAAGAATAT | 56916 |
rs183497331 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211523 | TCCCATTGTGGGATA[A/G]TGCTGCGTTAGTTTA | 56916 |
rs183500922 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286918 | CGCCCAGACTGGAGT[A/G]CAGAGGCGCAATCTC | 56916 |
rs183516958 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266838 | TGCCTTTTAGAAATA[C/G]AAATATTCCGGAATT | 56916 |
rs183520047 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285430 | TGTGTATAAAAATAA[A/G]CACGTGTTCTTTCTT | 56916 |
rs183529402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247285 | AATAAGCACTGGGTC[A/G]AATCATATCCCTTGG | 56916 |
rs183537466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230206 | ATATACTCAGATCCC[C/T]TACTCTCTTTCTGTC | 56916 |
rs183544140 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247713 | TAACCCCTGGCAACC[A/G]CCAATCTGCCTTCAG | 56916 |
rs183547472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214469 | AGACCCGGTTTCACC[A/G]TATTAGCCAGGATGG | 56916 |
rs183627302 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215888 | TTTGTGTTTCTTTAT[G/T]CTTTTCTGTTTTTCT | 56916 |
rs183692806 | snp | A/G | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272963 | CAGACATGCGCCACC[A/G]TGCCTGGCTAATTTT | 56916 |
rs183695276 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233869 | ACTGCAGATGTGTTG[C/T]ACTATGTATACACAT | 56916 |
rs183872142 | snp | A/G | 0.00114016 | 0.0238491 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290644 | ACAAAGTGAAATTTA[A/G]AAGTGAAGTTGTCTA | 56916 |
rs183955179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268515 | TGAATAGGATGACTA[A/G]AGAATTGGGAAGGAT | 56916 |
rs183960830 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287224 | TAAGGATGTAATGGC[A/G]TCTCTTATTTACTCG | 56916 |
rs183969484 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248151 | ATGGTTTCCAGCTAC[A/G]TCTGTGTTGCTGCGA | 56916 |
rs183985277 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231438 | GAGCAAGTGGTCAAC[A/T]CTGTTGTTCTTACAG | 56916 |
rs183993947 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277278 | TGAAGTAACTTTAAG[C/T]AGGTGATAACTCTAT | 56916 |
rs184060882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214149 | ACAGTTTCAGTAGAA[C/T]GGTGATGAGATAGAG | 56916 |
rs184161927 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235697 | AGGGCTAAAGTATTT[C/T]AAAGCAGTAATAAGG | 56916 |
rs184251914 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275207 | TGCCTAGTTATTGAA[A/G]AAAGTCGTCTTGTAA | 56916 |
rs184266956 | snp | A/G/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94253644 | GCCTATAATTCAAGC[A/G/T]TTAGGTGAAGGGAAG | 56916 |
rs184269545 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283805 | CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTCC | 56916 |
rs184272658 | snp | C/T | 0.000562532 | 0.0167616 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237060 | GTCGATTTATTGTTA[C/T]GTCATAATAATAGTA | 56916 |
rs184274557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220495 | TCAAGTGATCTGCCC[A/G]TCTCGGCCTCCCAAA | 56916 |
rs184304597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252275 | TGTAAGCATCATTCT[A/G]CTATATTCTTCAGTG | 56916 |
rs184323679 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219039 | CTAGTCTCGAACTCC[G/T]GACCTCAAGTGATCT | 56916 |
rs184375723 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278191 | AGTTCAAATTGATTA[C/T]TTCAGTAGAGAACAT | 56916 |
rs184382500 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241273 | TTTCTTTTCTTTCAC[A/G]GCTAAGCCAGATAAT | 56916 |
rs184384446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258095 | TTATTTTCCTATATA[C/T]TTGTCATTAGGTCAA | 56916 |
rs184402591 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224461 | AAAACCCAGCTGATC[C/T]GTATTTCACATACAC | 56916 |
rs184405393 | snp | A/T | | | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207332 | GTATTATTACTATTA[A/T]GCTATCTACATTATA | 56916 |
rs184702628 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258805 | AATTAAATGCCATCA[A/G]TTGCCTGGCTCTTTA | 56916 |
rs184736007 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225134 | ACTTTATTGACCTGT[G/T]TTTGAACAGACAGAT | 56916 |
rs184769877 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287880 | AAGCAGTGGCTGGGC[A/C/G]TGTGGTTCATGCTTA | 56916 |
rs184783149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269138 | ATGGGAAATGTTTTA[C/T]AAGTTGCATACCCCA | 56916 |
rs184848566 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94279184 | TTTTTTTTCAGACCA[C/G]GTCTGGTTCTGTTGC | 56916 |
rs184858325 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242201 | ACCACGCCCAGCTGT[C/T]TTTTTGTTTTTTTTT | 56916 |
rs184864577 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283018 | TACTAAGAGATGTAC[A/G]TACATCTTCAGGTTT | 56916 |
rs184867482 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207724 | GTTACATAGCACTGA[C/G]GCTACAAGATCGTAA | 56916 |
rs184899328 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245662 | GCTGTAACTCTTCCA[A/G]TGTCCACAAGCAAAC | 56916 |
rs184906182 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219415 | AGCCTTAATCTCCTA[C/T]TAGTGATTTTTTGTT | 56916 |
rs184909841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210558 | ATTGAGCTTAATGAT[A/G]GCGGTAGAAATGGAG | 56916 |
rs184986681 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262405 | GATCGTGAATCTTAT[C/G]AGTTTCTCCGTGTCC | 56916 |
rs185003660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227884 | TCAGTGTAAGGGACA[C/T]TAGTATAGTATAGCT | 56916 |
rs185042174 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223909 | CTGAAGTGTCAGAAA[A/G]TAGGACTTTATTGTT | 56916 |
rs185062259 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206956 | TGACTAAAATAACTG[A/G]ATTGTTTGAAACACA | 56916 |
rs185087610 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288673 | GGGAGGAGGAGAGAA[G/T]TGGTTAGTTTTGCTA | 56916 |
rs185127056 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229646 | AGTAGGAAATGATAC[G/T]TGGAAATATAGAAAC | 56916 |
rs185133206 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213297 | CAAAAAGTCACAGAG[A/G]TATGACCTTTGGAGT | 56916 |
rs185302133 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210075 | TTAGTTATTTATCAG[C/T]ATTGGTCATGTGAAA | 56916 |
rs185490821 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285237 | AAATACTAAAATAAT[A/T]TTTTTGAAGTTTCTT | 56916 |
rs185498311 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246854 | ATTAAACCTGCCAAG[A/T]TAAAAACGGATTGTT | 56916 |
rs185505235 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265901 | ATTAAAATTAATTGC[C/T]TTAGTTGCTGATTTT | 56916 |
rs185513272 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291684 | AACAGTTGGCATTAT[C/T]GTGTAGTGGAGAGAC | 56916 |
rs185632075 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271589 | AGTAATCTTTAGCAT[C/T]GTAAGATATTTTCCC | 56916 |
rs185642584 | snp | A/G | 3.29717e-05 | 0.00406015 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289560 | GTGAACTCTCAATTG[A/G]TGAGGAAATATCAAC | 56916 |
rs185646280 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249432 | TAAAGTTTGAGTTAC[C/T]GGATATGCAATCAGG | 56916 |
rs185659210 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274106 | TTGGATGTAGAAGTT[A/G]GAATAAGAGAATATT | 56916 |
rs185662158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217205 | TTTATTTCATTATAG[A/G]GACTAAAGAAAGGGT | 56916 |
rs185663972 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248490 | TTTCAGTGTGCCTGG[A/G]CTGTAAAGGTGGCAG | 56916 |
rs185664222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233228 | CATTCTCTGATCTCT[A/G]TAACTTACATTCATT | 56916 |
rs185671060 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244130 | AAAGAAAGATTGTCA[A/G]ATATTTGGATTCAAG | 56916 |
rs185673938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236373 | TAGAATGATGTCATG[C/T]AAGCAATATATGCAT | 56916 |
rs185675535 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216450 | ATGTCTGTTAATTTT[A/T]AAAATTATGATAAAA | 56916 |
rs185686745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240425 | TTTGTGAAATAAAAA[C/T]GTTACCTACTTTGTA | 56916 |
rs185760557 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275460 | TACATTAGTTGATTT[A/T]TTTAAAGTTCTATTT | 56916 |
rs185769137 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238304 | GCTGTGTGACCTTGA[G/T]CAGTGTTGCTTGACT | 56916 |
rs185804891 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232490 | AAAATTCAAAGTTGA[A/G]TACATCAGGAATGAG | 56916 |
rs185889789 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254372 | GCTCAGGCTTGTTGA[G/T]ATTCTAATTTATTTA | 56916 |
rs185911709 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221444 | TGGGTTTAGTATCAA[A/T]GAAAAATATTCACAA | 56916 |
rs186052685 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259992 | GTCCACTTATTAAGA[C/T]TGCTTGATAGGTCTT | 56916 |
rs186056746 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280423 | TAAGGACTTCTCCCC[C/G]TTTATTATACCTAAA | 56916 |
rs186202735 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264321 | ACATTTGATACTATT[A/T]CCTTTGGTATTAGGG | 56916 |
rs186202907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222517 | CCACTTGGTTCAGTA[C/T]AGTCTGCATGTTTAA | 56916 |
rs186206909 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284460 | CTGGAGTGCAGTGGC[A/G]CCATCTCTGCTCACT | 56916 |
rs186206982 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238896 | TACTAGGTAGCACAG[A/G]CTGTGGCTTAGGTAC | 56916 |
rs186219337 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246300 | AATTTTTTGTATTTT[C/T]AGTAGAAACGGTGTT | 56916 |
rs186268258 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260504 | GTGCACCACCACACC[C/T]AGTTAATTTTTGTAT | 56916 |
rs186353723 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259445 | ATTGTTATTAGATAG[A/C]TCTAAATTCTAAATC | 56916 |
rs186362543 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243327 | GGTACCATGAGAGTC[A/T]GAGACATCTGCACAT | 56916 |
rs186366306 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225448 | TAATTTTGAGGGTAC[A/T]ATCTCCAAATATAGT | 56916 |
rs186372645 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208205 | CTAATTGTTGCGGCC[G/T]AACAATGAAGCGCAG | 56916 |
rs186399415 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284546 | AGGATTACAGGTGTG[G/T]GCCACCACACCCAGC | 56916 |
rs186417891 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281091 | AAAGACACTATTTGT[G/T]AGTTATTTAAGTAAT | 56916 |
rs186443332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244469 | AATATCTGTTATGAA[C/T]GCATGCCTCGAATAA | 56916 |
rs186453847 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246700 | ACCCACTACCTGTAT[C/G]AAGTCCAGTCAACAT | 56916 |
rs186468373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212941 | CTTAACCTCTGCCCC[C/T]TGATTTATTTTACTC | 56916 |
rs186470558 | snp | C/T | 0.000649351 | 0.018007 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290303 | TTGATTTCCCTCTCC[C/T]GGCTTTTGCTTCTCT | 56916 |
rs186562700 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232706 | ACCTGTTATCCCAGC[A/G]CTTTGGAAGGCCAAG | 56916 |
rs186564339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208294 | CTGCTGTGGCATTGT[A/G]TCGTATATTGTTTTC | 56916 |
rs186627940 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265100 | CCAAGTAGGGTATTT[G/T]ATTCTATCATATCAT | 56916 |
rs186645782 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229149 | ACCATTTTTCCCTTT[A/G]TAATAAATAAGTTAT | 56916 |
rs186777463 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268682 | CATTGCAGATACAGA[C/T]TTGGTTAGCTACATG | 56916 |
rs186780316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225693 | TATATAATCTGATTT[C/T]ATATGCATATTAACT | 56916 |
rs186782486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248923 | TCTTGTGTGTATAGC[A/G]TGTGGTGCAGTTCTA | 56916 |
rs186784857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287602 | CCATTCTATACCTAC[C/T]TAGTCAAAAACTCTG | 56916 |
rs186816452 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216794 | GAATAATATTTCACT[C/G]TGTGTATATACACAT | 56916 |
rs186893633 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94290823 | ATTTATAAATCAAAG[A/G]TTTGTTAATTTTTGG | 56916 |
rs186907418 | snp | A/G | 0.000343623 | 0.0131032 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273739 | ATACTGGAGACAACT[A/G]TATTTAACTTTATCA | 56916 |
rs186924477 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252142 | GGCGTGAGCCACCAT[A/G]CCCAGCCTATTTGAA | 56916 |
rs186932535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235360 | GCTGTTGCAGGATGT[A/G]CTTTGTTCCTTTTAA | 56916 |
rs186932759 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218569 | AAGTGTTGGGATTAC[C/T]GCACCCAGACTCCTT | 56916 |
rs187053047 | snp | A/T | 0.00489472 | 0.049228 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276505 | TAAAGTTTTCCAAAT[A/T]ACTGTAAAATTTAGA | 56916 |
rs187065529 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215119 | TCATAATTCCGTGAC[A/C]ATTGCGCAATACTCA | 56916 |
rs187068369 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255333 | TGCATACTTGAGCCC[A/G]TGAATAAAGTACATA | 56916 |
rs187080279 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222762 | GATGTCAGGAGTTCA[A/G]CACCAGCCTGGCAAA | 56916 |
rs187123453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254928 | AGCCCAAACCCTACC[C/T]TAGAGCAGATTTAAT | 56916 |
rs187159138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228758 | AGTCAGTCCCTGGAC[C/T]ATATTTTCAGTAGTA | 56916 |
rs187204773 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218216 | CTCCTTTAGGTTTAA[C/T]GCTTTTGCCTTGTTC | 56916 |
rs187273616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279737 | GACTTCCATAATGCA[C/T]TTCTTTTTCATTTTA | 56916 |
rs187273689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94251231 | GATATCAAAAGCACT[A/G]GCATCAAAAACTTAA | 56916 |
rs187281314 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276129 | AATTATGTATTGCAG[A/C]TTTCATAGCTTGGTT | 56916 |
rs187303032 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217930 | GTTACACTTGCAAAT[C/T]TAACAATCTGTGTGC | 56916 |
rs187359998 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212627 | AAGTAGCTGAGACTA[C/T]AGGTGCACACCACCA | 56916 |
rs187462334 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272273 | GAGGTTACGACTCCA[A/G]CGTATGTATTGTCAG | 56916 |
rs187469406 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233684 | TGCGTGTGAGTCCTA[A/T]CAAAATAAATGCTAG | 56916 |
rs187539498 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234197 | TATAGTTAGTAGTGG[A/G]TAGTCATTTTTCTAA | 56916 |
rs187645094 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261806 | GTAGAGATGGAGTTC[C/T]GCCATGTTGCCCAGG | 56916 |
rs187656050 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282193 | CAAGCTCCGCCTCCT[A/G]GGTTCACGCCATTCT | 56916 |
rs187769871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239793 | GCCAAGGCTGATCTC[A/G]AACTCCTGAGCCCCA | 56916 |
rs187780555 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206486 | GAACGATGGCTACCA[A/G]AGGCTGGGAAGGGTA | 56916 |
rs187785124 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286143 | AGGGAAATTTTTCAA[C/T]CTCCTGTGAAGTGAA | 56916 |
rs187793331 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256828 | GTGTAAGTTTGATAA[A/G]TTTGTATTAAAAAAA | 56916 |
rs187797252 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266846 | AGAAATACAAATATT[C/G]CGGAATTCCTTGTGA | 56916 |
rs187802085 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240530 | AGAAATTGCTGGTTT[C/T]TGTGATGGTATTCAG | 56916 |
rs187805729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224165 | GTGATTTATTCCACT[A/G]CAGAGTTGTTTGCTC | 56916 |
rs187817945 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207033 | ATTACACATTGCATG[A/C]CTGTATCAAAATATC | 56916 |
rs187924105 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226424 | TTTTTTGCCCCACCT[G/T]CCTTTCTTGGCCACA | 56916 |
rs187924301 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281382 | TTTATCAACATGATA[C/T]AAGTAACACTTCTAA | 56916 |
rs187936408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245334 | TGTGTATGCCATGAC[A/G]GTGTAATACAAATGA | 56916 |
rs187937602 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261186 | ATAAAGATTCAGTGT[A/G]CTTCAGCTTCACTTT | 56916 |
rs187954118 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226887 | TTTCTTGTTTTTTCT[A/T]GAGGTGGGGTCTTGC | 56916 |
rs187956207 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94209819 | GTTCACTCTTTGAAT[A/G]GATATTTGACATCCA | 56916 |
rs187997861 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286957 | GCAAGCTCCGCCTCC[C/T]GGGTTCACACCATTC | 56916 |
rs188010122 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247799 | ACCTTTTATGTCTAG[C/T]CTCTTATTTTTTAAT | 56916 |
rs188032525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256157 | TAATCAGAGTAGTAA[C/T]GTTTTTATGCTGACC | 56916 |
rs188056202 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223605 | CAGAGTTAAGCTTTT[A/G]TTGCCCAGGCTGGAG | 56916 |
rs188149214 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284044 | GAGGTGAAGATAGCC[A/G]GGCACGGTGGCTCAC | 56916 |
rs188211754 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209269 | TAGTGATAAGTGCTT[A/C]ACCTTCTGTCATTTA | 56916 |
rs188300949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268148 | TATATTTTTATAACA[A/G]ATATTTCAATGTAAT | 56916 |
rs188302917 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231133 | TAGAAAATCAGTCTA[A/G]TAAAATCTGTGAAAT | 56916 |
rs188304603 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248250 | TCATTCATGTTGTGG[A/T]GTGTATCAGTACTTC | 56916 |
rs188320725 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215925 | TGTCTCTCCGATAAA[C/T]TATTTGTAAGTATAT | 56916 |
rs188322230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232309 | TTGTTAGATCATTGA[A/G]TCTGATCACTGGATA | 56916 |
rs188337041 | snp | C/T | 0.00874735 | 0.0655527 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94205905 | CTGGTTCATGCCATT[C/T]TCCTGCCTCAGCCTC | 56916 |
rs188458715 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210561 | GAGCTTAATGATAGC[A/G]GTAGAAATGGAGAAG | 56916 |
rs188533460 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275409 | CTTGGTAATAATTGA[A/T]GTAAATATCTTGCAC | 56916 |
rs188540040 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245628 | AACCTGTTTTTTGCC[A/T]CTTTACAATAACTCG | 56916 |
rs188547700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237329 | CTTAGTAGGAACATA[A/G]TGTCTTAGGGAAAGG | 56916 |
rs188549907 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94253852 | TTTATAGCAGGAATT[A/G]TATATAGGCCTGTTG | 56916 |
rs188556721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210248 | CAGCCTTGATGGCTT[C/T]GGGAAATAAGAAAAC | 56916 |
rs188561571 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273121 | TATTTAGGTTATTTC[C/T]AGTGTTTGGCTATTA | 56916 |
rs188684860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94278802 | CATTTTGTTTAGTCA[C/T]ATAATGGGATTTGTG | 56916 |
rs188689069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232896 | GAGGTGGGAGGATTG[C/T]TAGAGCCTGTAAGAC | 56916 |
rs188691211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241434 | TTTTTATAAGGACAA[C/T]AGTCAGATTAGGTCC | 56916 |
rs188694832 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216834 | CCATTCATCCATCAA[C/G/T]GGGCACTTGGATTGC | 56916 |
rs188698456 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258739 | CATATCTGTAAGCAA[A/C]TATCTGTAAGTGGGG | 56916 |
rs188707764 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230822 | TTCAGCAGTTGAAGA[A/C]GGTGAACAAAGGAAG | 56916 |
rs188780707 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291413 | GCCTGTTTGCCAGTA[A/C]ATTGGAACTTACTAC | 56916 |
rs188829387 | snp | A/G | 0.00247422 | 0.0350855 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290666 | AGTTGTCTATTTGAT[A/G]TTTAACTCTTTATTA | 56916 |
rs188835642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227698 | GAAGGAAAGTCAGCA[A/G]TTCATTCTTGAACAT | 56916 |
rs188837559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94251946 | AACCTCCACCTCCCA[A/G]GTTCAAGCGATTCTC | 56916 |
rs188937639 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277895 | TTCTATCTTCAGTTC[A/T]TAATATATGGAGGAC | 56916 |
rs188979505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247478 | CTAAATATTTGATTC[C/T]GAAGAGCTGTTTACT | 56916 |
rs188989954 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214202 | GAGAGAAATAGGTAA[A/C]CTGATTGGGAAGTAA | 56916 |
rs189037800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284525 | TGCCTTAGCCTCCCA[A/G]CTGCTAGGATTACAG | 56916 |
rs189074433 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274045 | GAATTAAACAGATAC[A/G]TAATTAATTCCTACA | 56916 |
rs189082376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236058 | TTTTAAATCCATGTA[A/G]AAGAATTCAAGAGGT | 56916 |
rs189173803 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280117 | TGATTTACCCACCTC[A/G]GCTTCCCAAAGTGCT | 56916 |
rs189181141 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287936 | CGGGAGGATCGTTTG[A/C]GCCCAGGAGTTCAAA | 56916 |
rs189187123 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259972 | TGAATTAAGATCCAA[G/T]TAAGGTCCACTTATT | 56916 |
rs189209510 | snp | A/G | 1.69189e-05 | 0.00290846 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94253058 | GTGTGTATTTAATTC[A/G]CAGTACCGGTTATAG | 56916 |
rs189225948 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220115 | TTAGCCATTGGCTGT[C/T]AGCTATTTTGCTGTT | 56916 |
rs189228607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236411 | TGAAAAGATTCAGAC[A/G]ATTCAGAAATAGAGT | 56916 |
rs189286305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279326 | TAATTTTTTTGTACG[A/G]ATGGGGTTTTGCCAT | 56916 |
rs189320429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242489 | CCATCTCTTGGTACA[C/T]AAAATGGGCAACAAG | 56916 |
rs189327890 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246197 | TGATCCTGGCTCACC[A/G]CAACCTCCGCCTCCC | 56916 |
rs189333587 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94263228 | TTCTCTCACATTTCA[A/G]TGTATTACACACACA | 56916 |
rs189334154 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207833 | CTGTGTGTTCTTAAT[C/G]CTATCAGCTTCCTCT | 56916 |
rs189352230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212336 | CATGCCACCATGCCC[A/G]GCTAATTTTTGTATT | 56916 |
rs189455176 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262411 | GAATCTTATCAGTTT[C/T]TCCGTGTCCAACACA | 56916 |
rs189467102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228348 | TCTTCGTAAACAGCA[A/G]TTACAATAACTACTG | 56916 |
rs189582586 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259009 | CATGCCCACCCTATA[G/T]CTTTTTAAATCAGAT | 56916 |
rs189598449 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224541 | ATCAGATGTGGAATT[G/T]TCCACTCTTGGAGTC | 56916 |
rs189611316 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225157 | AGACAGATGATACCA[A/G]TCATACTAGTTTTCT | 56916 |
rs189713182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283360 | CTTTAATTTGTGTAG[A/G]CCATTAGAATATAGT | 56916 |
rs189733209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221311 | AAATGACCAAAGCAC[A/G]GTATTAGGAAATAAT | 56916 |
rs189742364 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245790 | TGATGAAGTTTTTGA[C/G]ATTGTATCTCTAACA | 56916 |
rs189801575 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266783 | GTTTACTTTGCTACA[A/G]ACTGTTGCAAATTTA | 56916 |
rs189809438 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285325 | AAATGAAAGAACAGA[C/T]GCCTCCTAGTCGCCC | 56916 |
rs189809781 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246862 | TGCCAAGATAAAAAC[A/G]GATTGTTTCTGTTTG | 56916 |
rs189830456 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213469 | GAAACTGAAAAGATA[C/G]AAGTGTAAACCATTG | 56916 |
rs189832534 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229837 | TGTTTACAGTGATAC[C/T]GATAATTCTAATCTA | 56916 |
rs189884821 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207475 | GATAATTTAACAGGA[C/T]AAAGGTACAGAACAA | 56916 |
rs189930098 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276858 | GCTGTTGATAATAGC[A/G]GACGTCAATTATTTA | 56916 |
rs189942066 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255580 | TATATAAAATGTAAG[G/T]ATAATATACTTATTA | 56916 |
rs189954449 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271962 | TCAGCTAGCATTGCC[A/G]TAACAAAATACCACA | 56916 |
rs189958784 | snp | C/T | 0.000515172 | 0.0160412 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289712 | CTCCAAATACTCACA[C/T]GTGAAATTTCAAAAA | 56916 |
rs189968705 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250054 | TGTAACCCTGCCCCC[A/G]TCAAGTAACTGCTTA | 56916 |
rs189970360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209374 | TAGGAACTTGGTAGA[A/G]CCTGAACTCAAGTCC | 56916 |
rs189971824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289268 | ACCTTAGATTGCTAT[A/G]TTGGCAATATGAACA | 56916 |
rs189978392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233415 | AAGTTAGTTGTTGGA[A/G]AATAAACCCTCATAT | 56916 |
rs189980171 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217257 | CATTATTCACCAGTT[A/G]CTAGTCAGTTTTTCA | 56916 |
rs189980698 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249217 | CCATTCTGTGAATCA[A/G]GAGTGAAGTAAAAGT | 56916 |
rs190097971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229252 | CTATTGATTTTTGTC[A/G]GATTAATTTATGATA | 56916 |
rs190108210 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212963 | ATTTTACTCTTCTCG[A/G]TGCCCAAAGTTGTCA | 56916 |
rs190114494 | snp | A/C/T | 0.00129554 | 0.025419 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275007 | TGGATATTTATGCAG[A/C/T]CCCCAAATTTAAAAA | 56916 |
rs190238729 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271081 | TACAAATTAAAAAAT[C/T]GAAATCAAAGTCACC | 56916 |
rs190258554 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269589 | TGAAAAATGATATCT[C/G]TGCCTATGTATAATA | 56916 |
rs190267263 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232532 | TAATAATGCAAAGGA[A/G]ATGCATGTGATTGTC | 56916 |
rs190349410 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264626 | TAAATTAGCAAACTT[C/G]TTTTCCTCATAAAGA | 56916 |
rs190382731 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229009 | AAATGATCTTGTGTC[A/G]TCCTCAGTGTGTCAT | 56916 |
rs190449470 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94251998 | CTGGGATTACAGGCA[G/T]GCACCACCATGCCTG | 56916 |
rs190468056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260186 | AACGATCATTAGAAG[A/G]TTAAATGCACCCACC | 56916 |
rs190473077 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234350 | TTAAAGCCTTAATAG[C/T]GAACATAGGTTGTGA | 56916 |
rs190474922 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94280681 | TGTACTTTGTAAACA[A/G]TACCGACACATTAAT | 56916 |
rs190517295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248700 | CAAGTAGACCACTTA[A/G]TATTATGAAACACAT | 56916 |
rs190536006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216638 | GATTCCCCCAGCCCC[C/T]GGCAACTACCGTTTA | 56916 |
rs190591086 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276158 | TTACAGTGTACATCA[A/G]TAATTATTAAATACA | 56916 |
rs190608169 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254995 | ATTTTTTAGTTAAAA[G/T]CTATATAATTTGCTT | 56916 |
rs190617737 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222539 | CATGTTTAATGTATA[G/T]ATTTTGAGAGTATAT | 56916 |
rs190617917 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239207 | GTTTGTCTAACCTTG[A/T]AGATAAGGTTAATCT | 56916 |
rs190750651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243847 | GAAAAAAGCACTCAT[C/T]CAACATCTCAAACCT | 56916 |
rs190763979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254472 | AAAGTAAATTATACA[A/G]TTTTACCAGAGGTAT | 56916 |
rs190767436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225510 | AGTTAAACCTTAATT[A/G]CCTTTTTAGAGGCCT | 56916 |
rs190769457 | snp | A/G | 0.000660575 | 0.0181618 | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208210 | TGTTGCGGCCTAACA[A/G]TGAAGCGCAGCCATA | 56916 |
rs190854742 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281144 | GCCTAAATTTGTAAA[A/G]TCACAGTCCAGATAA | 56916 |
rs190887386 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244869 | CTCCAAAAACCACCT[C/T]TCTGATAACAGCCCC | 56916 |
rs191009523 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239699 | CGCCTCAGCCTTCCA[A/G]GTAGCTGGGACTACA | 56916 |
rs191016308 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275722 | ACTTCATGGAGCAGA[C/T]TACTTACAAGTTATA | 56916 |
rs191016694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238424 | TATGGTGCCTGGTAC[A/G]TAGTGAGTGCATACC | 56916 |
rs191029810 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265654 | TATTTTTAAGTAGTT[A/T]GGAGACTCAGAACTG | 56916 |
rs191036417 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206186 | TCGAAATGATATCTG[C/T]ATTCTCATGTTTGTT | 56916 |
rs191126505 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260563 | TGGACTTGAACTCCT[A/G]GGGCCTCAAGTGATC | 56916 |
rs191193581 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269077 | TTATAAAAGGCAGAA[A/T]TAGAAATACTGCTTT | 56916 |
rs191204352 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287676 | GATTCTGATAAAGCT[A/G]AAATCAGAGAACCAC | 56916 |
rs191217031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248353 | TATTAACAAATGAAC[A/G]ACTGAAGTTTAGTTT | 56916 |
rs191227272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232311 | GTTAGATCATTGAGT[C/T]TGATCACTGGATAAA | 56916 |
rs191254950 | snp | C/G | 4.95062e-05 | 0.004975 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94284991 | AAACTAATAAGCCAA[C/G]GGACGATTGAAGAAT | 56916 |
rs191263255 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223435 | GAGGCGGAGGTTGCA[A/G]TGAGCTGAGATCACG | 56916 |
rs191267470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246728 | CATGATGTCAGTATA[A/G]TGGATCAAGTGATAC | 56916 |
rs191332831 | snp | C/T | 0.000203438 | 0.0100835 | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291305 | TAAGTTGTATTTTCA[C/T]ACCCTTTTTAATAGT | 56916 |
rs191345371 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273866 | TCTTTATACTTTTCT[A/C]CTTTGTTTATATATG | 56916 |
rs191351468 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228471 | TACCAATTAACACTA[C/G]TACAGTACTATTATC | 56916 |
rs191355323 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210679 | GCGCGGTGGCTGAAG[C/G/T]CTGTAATCCCAGCAC | 56916 |
rs191361815 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235424 | ATGCTATTCAAGCCA[A/G]ACAACACATGTCTGT | 56916 |
rs191362158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252172 | ATAATTTTTTAAGTA[A/G]CGATGCAACTTAGAA | 56916 |
rs191398320 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206920 | TGAGCCACCACTCCC[A/G]GCTTATTGTACATTT | 56916 |
rs191484574 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247867 | AACTTTATGTTAGAA[A/T]TGGGGTACATGTGCA | 56916 |
rs191508924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215441 | GCTTGGGCAATGTAG[C/T]GAGACCCTGTCTCTA | 56916 |
rs191527262 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290738 | TTTTATTATACATCA[A/G]TTTCTTTGTATAACT | 56916 |
rs191649755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286279 | CTCTTTCTTCTCTTC[C/T]ATGACAAGTCCAGAG | 56916 |
rs191777012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273401 | TAGCAATGAAGATCT[A/G]TCCACTGCTCAGTAA | 56916 |
rs191814738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244157 | CAAGACCAAAGGGTG[A/G]AAAACTTAAGGAACA | 56916 |
rs191818695 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272404 | ATGATGTCTAATTTA[G/T]TTGCAGTAAAATGTA | 56916 |
rs191826366 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233852 | ATTTACTATTGAAAA[G/T]AACTGCAGATGTGTT | 56916 |
rs191843509 | snp | G/T | 8.25348e-05 | 0.00642344 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208412 | GAATCTTTTCAACCT[G/T]GACCGTTTTCGCTTT | 56916 |
rs191939010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94278871 | TAAAACTTAGTTGAT[A/G]TATTTCAACAGTTAT | 56916 |
rs191968839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221586 | TAGAAACAGATATGA[A/G]AATCCAGCCATCTTG | 56916 |
rs192074551 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218395 | TCCTGAGTAGCTGGG[A/T]CCTCCTCCTGACTCA | 56916 |
rs192093151 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282976 | GGAGGCTCTTCAGTG[A/G]TATAGCCAGAGGAGA | 56916 |
rs192105063 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290584 | TTTCCAGTACAGGAC[C/T]GCCTGAAGAGAGAGC | 56916 |
rs192131495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94251653 | ATAAAGGTATGATAA[C/T]CTGTGTAAGTCTAAT | 56916 |
rs192135797 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217932 | TACACTTGCAAATCT[A/T]ACAATCTGTGTGCTT | 56916 |
rs192210606 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278127 | AGAGTTATCTAGGTA[A/G]TCGATACATGACTCA | 56916 |
rs192227194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241141 | AGGGAATTTACGTCT[A/G]CATTTAATTTGTGAC | 56916 |
rs192235648 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256837 | TGATAAGTTTGTATT[A/T]AAAAAATCTGCAAGT | 56916 |
rs192246561 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224338 | ACTTGGTTGTTGTTA[C/G]AGGTTGAGTATCCCT | 56916 |
rs192250243 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207045 | ATGCCTGTATCAAAA[C/T]ATCTCATGTACCCTA | 56916 |
rs192255697 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256178 | TATGCTGACCAATGC[A/G/T]ACATGCATCAGTAAC | 56916 |
rs192283475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223872 | AGGTGTGAGCCACCG[C/T]ACCTGGCCTCTCATA | 56916 |
rs192354080 | snp | A/G | 0.00121969 | 0.0246649 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281433 | TTTGAGTAGTAAAAC[A/G]ATTTTTTCTATTTCT | 56916 |
rs192360695 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245458 | GATGAATTTGGAACC[A/G]TACAGGCAGCTTTAG | 56916 |
rs192364519 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283562 | CGGGCGCCGTGGCTC[A/T]CGCCTGTAATCCCAG | 56916 |
rs192366734 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261515 | ACTGTGAATAGTTAC[A/G]TATTTAATTACTCAG | 56916 |
rs192370424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227127 | AAAGTGAACCATGTA[A/G]ATGTGGGGGAAAGAG | 56916 |
rs192389119 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210040 | AAAGCAGTTTGTAAA[C/G]TGGATTTCAGTGGAA | 56916 |
rs192390042 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246056 | CGGAGTACCTTGTAT[C/T]GCACTCTGGACCTGG | 56916 |
rs192418275 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218910 | TCTGTCTCCTGGGTT[C/G]AAGCAATTCTCATGC | 56916 |
rs192531330 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268345 | CAATGTGTGTTGGTG[A/C]TGAAGAATTTCAGTA | 56916 |
rs192657303 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277207 | GTTATTTGTGTTTTA[A/T]CTGGGCCATTCTTCT | 56916 |
rs192673745 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216076 | GCTGCAAGATTAGGT[A/G]TCTCAGGGCCCTATT | 56916 |
rs192687813 | snp | A/G | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240185 | TAGTAGCACAGCAAT[A/G]TGTCTGACAAACTTG | 56916 |
rs192746090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262606 | ACCCTTACTGCCTTC[C/T]TGTTCAGACTTGTCT | 56916 |
rs192866407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262089 | AATTTCATGTGCTTT[C/T]CCTTAGGTAATCTCA | 56916 |
rs192880844 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227739 | AGAACACTCCTAGAC[A/G]TCTAAATGGAGATGT | 56916 |
rs192950179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247604 | CATTCACAGTGTTGT[A/G]TACCATCATTCCTGT | 56916 |
rs192958640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214402 | GAGTAGCTGGGACTA[C/T]AGGTGCCCGCCACCA | 56916 |
rs193002251 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236086 | GGTTGTGAAATAGTT[A/C]TAAGCTTGCTAAGAA | 56916 |
rs193009945 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287087 | GCCAGGATGGTCTTG[A/T]TCTCCTGACCTCGTG | 56916 |
rs193084502 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245630 | CCTGTTTTTTGCCAC[A/T]TTACAATAACTCGTA | 56916 |
rs193088655 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210294 | AATGTTGAGAATTAA[G/T]CCTTGTAGGAATGGA | 56916 |
rs193161123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274090 | ATTCTTTCTCAATTC[A/G]TTGGATGTAGAAGTT | 56916 |
rs193174092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267514 | GTTGTTTCTATTTTA[C/T]GCCTTTCTCACCTTT | 56916 |
rs193177696 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230922 | AACCCCTGAGGTGAG[A/G]GTGGGGCCAAATTTT | 56916 |
rs193207788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219412 | ATGAGCCTTAATCTC[C/T]TACTAGTGATTTTTT | 56916 |
rs193298472 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291495 | GTAACCCATTATCAC[A/T]ACAGAGCAAATGAAG | 56916 |
rs199527805 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262912 | AAAAAAAAAAAGAAA[A/G]AAAAGAAATGGTAGT | 56916 |
rs199546608 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267077 | TCTATAATTTATCAG[A/C]CTTAAAAGATTTCTC | 56916 |
rs199546942 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207795 | AAAAGATGCCTTAGC[A/G]TGCACTCCACCTCTG | 56916 |
rs199619138 | in-del | -/TTAT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285101 | CAGAAACTTCAATAT[-/TTAT]CTATATGACCATGCA | 56916 |
rs199698571 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229802 | TGAAAATGTGTGGTG[G/T]TTTTTTTTTTTTAAT | 56916 |
rs199718824 | snp | A/T | 0.000181313 | 0.00951965 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94281540 | GGTTCTATTAAAACA[A/T]CATCAGCATAGGTAC | 56916 |
rs199721740 | snp | A/G | 3.55013e-05 | 0.004213 | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94278889 | TTTCAACAGTTATCC[A/G]CTTGGTTTTATTTTT | 56916 |
rs199743897 | snp | A/G | 6.59109e-05 | 0.0057403 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252918 | CTTCAAGATGCTTCA[A/G]TTGGTGAACTTACTT | 56916 |
rs199753081 | in-del | -/A | 0.0134861 | 0.0810011 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250194 | GTTTTCAGAGTCATT[-/A]AAAAAAAAAGACTCA | 56916 |
rs199819739 | in-del | -/A | 0.0138799 | 0.0821421 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206390 | ATAAGGCAGGCACAG[-/A]AAAAAAAACTTGGTA | 56916 |
rs199891976 | snp | C/T | 6.59642e-05 | 0.00574262 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94276402 | GCTGAAACTTAATTA[C/T]GCAATTTTTGATGAG | 56916 |
rs199893762 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239562 | TAGCTGCCCTGTTGT[G/T]TTTTTTTTTTTTTTT | 56916 |
rs199959460 | snp | A/G | 0.00104732 | 0.0228596 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280828 | TTCTCAATTACTTTA[A/G]CTTCTTAAAGCAATT | 56916 |
rs199978200 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228794 | GGTAATTTTTTTTTT[-/T]ACAGTGGATTTAGTT | 56916 |
rs199979749 | snp | A/G | 8.25321e-05 | 0.00642334 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226251 | CCCCAAATTGCTCCA[A/G]TACAGTTCAAGAGAA | 56916 |
rs199980010 | in-del | -/CT | 0.0236746 | 0.106192 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286579 | AAAAGTTGTAGACAA[-/CT]CTCTGTCTGCTGTTG | 56916 |
rs200011317 | in-del | -/TTTATA | | | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252564 | TATTTGAAGTCTATC[-/TTTATA]TTTATGTATTTCTAA | 56916 |
rs200017835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270832 | TGGTAAGTGTACTTT[A/G]TTTCTAAGATTTGTT | 56916 |
rs200061807 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239376 | ACAAATTGCAGTCTT[A/T]ACAGACAGTATCATC | 56916 |
rs200103737 | snp | C/T | 8.39187e-05 | 0.00647706 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276312 | TTAAAGGTATAACCT[C/T]AGAGATGTTTTTTCT | 56916 |
rs200120921 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240300 | GTTTGTTTTCTTCCA[C/G]TCACGACAATATGCA | 56916 |
rs200143335 | snp | A/G | 3.30267e-05 | 0.00406353 | missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208407 | AATATGAATCTTTTC[A/G]ACCTGGACCGTTTTC | 56916 |
rs200181471 | snp | A/G/T | 0.000461119 | 0.0151774 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252757 | GCTTTAACAAGAAAC[A/G/T]TAAAAAAAATGTTTT | 56916 |
rs200193701 | in-del | -/T | 0.00468134 | 0.0481535 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281622 | TTAGTTACAAAAAAA[-/T]AACTCATTTATTATT | 56916 |
rs200194206 | snp | A/G | 0.000135853 | 0.00824065 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249613 | AGACCATTGTTATTG[A/G]TATCTCTTAAATTGT | 56916 |
rs200240216 | snp | C/T | 0.000863042 | 0.0207551 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278604 | TATCTTAAACTGTTT[C/T]TTCTGTCTCAGGTTC | 56916 |
rs200242031 | snp | A/G | 6.78342e-05 | 0.00582344 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283089 | TTATACAACTTTTTA[A/G]TGAGATTTAACCTAA | 56916 |
rs200310469 | snp | A/G | 0.0245038 | 0.107942 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276993 | GCTCTTTAAGAAAAA[A/G]CTAATATAAATTTTA | 56916 |
rs200397023 | in-del | -/GC | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245935 | TCTTTAAAACTCTCT[-/GC]AAAACGATTTTCCCA | 56916 |
rs200421294 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267080 | ATAATTTATCAGCCT[A/T]AAAAGATTTCTCACA | 56916 |
rs200445498 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218291 | AATTGTTTTATTTTA[-/T]TTTTTTTTTTGAGAT | 56916 |
rs200454016 | in-del | -/TGT | 0.0271762 | 0.113356 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269664 | CTATTGTTTTCATTC[-/TGT]TGTTGTTGTTGTTGT | 56916 |
rs200474815 | in-del | -/TACT | 0.0193772 | 0.0965046 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226553 | GATTTTGAGAGCAGA[-/TACT]TAATTTCCTTATTAT | 56916 |
rs200476496 | snp | G/T | 6.27622e-05 | 0.00560153 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289722 | TCACACGTGAAATTT[G/T]AAAAAAGAAGCCACA | 56916 |
rs200528750 | snp | C/T | 0.000248738 | 0.0111493 | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94278748 | GGTATAATCTGATTT[C/T]TACTCTTTTATGTGA | 56916 |
rs200556343 | in-del | -/AGCCATAATTTACC | 0.0310518 | 0.120672 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276719 | AATTATTAGGTCATA[-/AGCCATAATTTACC]TGTTCTATATGTTAA | 56916 |
rs200562832 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280981 | AAAAACAATAGAAAG[A/T]TAGTAGACTGTATCT | 56916 |
rs200569328 | snp | C/T | 0.00199792 | 0.0315431 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94264752 | TCAGAAGATTTGATA[C/T]GGCACTGTAAAACAC | 56916 |
rs200613683 | in-del | -/C | 0.0236746 | 0.106192 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257550 | AGTAGAGTGTTCTTA[-/C]ATCTTTCCTTAAGTG | 56916 |
rs200626666 | snp | A/G | 0.000164764 | 0.00907495 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94280686 | TTTGTAAACAGTACC[A/G]ACACATTAATAACTT | 56916 |
rs200628047 | in-del | -/A | 0.0111196 | 0.0737302 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235632 | TGTTACTTGTCTGCT[-/A]AATGTGAATTTTTTT | 56916 |
rs200698265 | snp | C/G | 9.8956e-05 | 0.00703336 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270709 | GATGTGTAATATTTG[C/G]TAACTCTCTCTTTAC | 56916 |
rs200700290 | snp | C/G | 9.09562e-05 | 0.00674313 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264912 | TAAACCAAAGGTAAT[C/G]TTTGTTGAATATATT | 56916 |
rs200726381 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284137 | CCATTCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 56916 |
rs200739794 | in-del | -/CTC | 0.49423 | 0.0534032 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282206 | TGGGTTCACGCCATT[-/CTC]CTGCCTCAGCCTCCC | 56916 |
rs200753490 | in-del | -/TCTA | | | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252558 | AGTTTTTATTTGAAG[-/TCTA]TCTTTATATTTATGT | 56916 |
rs200783225 | snp | A/C | 3.3248e-05 | 0.00407712 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283322 | AGTGTTTTTAGTTGG[A/C]ATGTATTTTTAATTC | 56916 |
rs200799135 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262913 | AAAAAAAAAAGAAAG[A/G]AAAGAAATGGTAGTT | 56916 |
rs200869648 | in-del | -/TTTCT | 0.0126979 | 0.078662 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272785 | TGAATATTTAGGTTA[-/TTTCT]TTTCTTTTCTTTTTT | 56916 |
rs200889387 | snp | G/T | 0.00199804 | 0.031544 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250847 | AGGTAATTATTCTGG[G/T]TCATAGAAAATACAT | 56916 |
rs200907600 | snp | A/G | 3.50067e-05 | 0.00418355 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94283130 | TTACAGGATTCATCT[A/G]ATTGATGAGTTTAAT | 56916 |
rs200908251 | in-del | -/TAAAC | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267079 | ATAATTTATCAGCCT[-/TAAAC]TAAAAGATTTCTCAC | 56916 |
rs200945389 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285105 | AACTTCAATATTTAT[C/T]TATATGACCATGCAT | 56916 |
rs200948051 | snp | A/G/T | 0.000181527 | 0.00952537 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226232 | GATAGTGAAGATGTC[A/G/T]TTTCCCCAAATTGCT | 56916 |
rs200966107 | in-del | -/ATAC | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226552 | TGATTTTGAGAGCAG[-/ATAC]TTAATTTCCTTATTA | 56916 |
rs200987324 | snp | A/T | 0.000923463 | 0.0214681 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280553 | CATATTATTAATTAT[A/T]TTTATTTTGAAGTAT | 56916 |
rs200993447 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265997 | AAAATCAAGGTATGG[-/A]AAAAAAAAACAAGAT | 56916 |
rs200998764 | in-del | -/ACTC | 0.0684985 | 0.171922 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289705 | CTGAATTCTCCAAAT[-/ACTC]ACACGTGAAATTTCA | 56916 |
rs201008964 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239578 | TTTTTTTTTTTTTTT[A/T]ATTTTTTATTTTGAG | 56916 |
rs201009518 | in-del | -/TA | 0.0310518 | 0.120672 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235497 | ACATTATTTTTAATC[-/TA]TGTTATTTTTGACAT | 56916 |
rs201013072 | snp | A/C | 1.73887e-05 | 0.00294857 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226107 | ATTTTTCTCCTTTTT[A/C]TTCTCTTGCAGAAGA | 56916 |
rs201049914 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280982 | AAAACAATAGAAAGT[A/T]AGTAGACTGTATCTG | 56916 |
rs201056294 | snp | A/G | 0.000265556 | 0.0115199 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276334 | GTTTTTTCTTTTGGT[A/G]ACAGATATAACTGTG | 56916 |
rs201064800 | snp | A/G | 0.000442809 | 0.0148731 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281618 | CATGTTAGTTACAAA[A/G]AAATAACTCATTTAT | 56916 |
rs201116246 | snp | C/T | 0.00199792 | 0.0315431 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226222 | TTTGTCTTCTGATAG[C/T]GAAGATGTCGTTTCC | 56916 |
rs201118788 | snp | C/G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246908 | GGGAAAAAGCAAGTA[C/G/T]TTGATTGATAACTGC | 56916 |
rs201203613 | in-del | -/TTAG | 0.0240643 | 0.107019 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209419 | CTGAGCATAAACTAA[-/TTAG]TTAGTTTCTTAGGAA | 56916 |
rs201210679 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272031 | ATTCTGGAGGTGGAC[A/C]GTCCAAGATGAGTGT | 56916 |
rs201247638 | in-del | -/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265400 | TCTCCTTTTGGGGTA[-/G]AAATACATCAGCAAG | 56916 |
rs201312778 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272091 | CTCTTTGACTTGAAG[G/T]CAGCCACTTTCTTAC | 56916 |
rs201332614 | snp | A/G | 6.62054e-05 | 0.00575312 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237061 | TCGATTTATTGTTAC[A/G]TCATAATAATAGTAC | 56916 |
rs201340263 | snp | C/T | 1.65116e-05 | 0.00287324 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208409 | TATGAATCTTTTCAA[C/T]CTGGACCGTTTTCGC | 56916 |
rs201401547 | snp | A/G | 0.00199806 | 0.0315443 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94264857 | GTTACCATGCTTACT[A/G]GAAATGGAGGTGGAT | 56916 |
rs201405700 | snp | A/C | 0.000282315 | 0.0118776 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278596 | AGAATGATTATCTTA[A/C]ACTGTTTTTTCTGTC | 56916 |
rs201412452 | snp | A/G | 7.97925e-05 | 0.00631585 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252726 | AAACAGAAATTTTCA[A/G]TGAAAGCACAAAATG | 56916 |
rs201413020 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232046 | GTTTTAATTTTTAGT[A/G]GAGATGGGGTTTCAC | 56916 |
rs201426312 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262909 | AAAAAAAAAAAAAAG[A/G]AAGAAAAGAAATGGT | 56916 |
rs201495706 | in-del | -/TCT | | | intron-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94253551 | AACATGTTTTTGTTG[-/TCT]GTTAAGCAACGTGGC | 56916 |
rs201507083 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286825 | TTTTAGCTGTGCTCT[G/T]AAGCCAATAGCTTTG | 56916 |
rs201562165 | in-del | -/T | | | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94279166 | ATATTTAAGAAAAAC[-/T]TTTTTTTTTTCAGAC | 56916 |
rs201564533 | in-del | -/ATAAA | 0.0069861 | 0.0586877 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234157 | GTAGCTGTAATGATG[-/ATAAA]ATCTCTCCTGCATTC | 56916 |
rs201583868 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239438 | CTGTTTGTTTTGAAA[G/T]TTTGTTTTTGAATAT | 56916 |
rs201635836 | in-del | -/AACTT | 0.00676609 | 0.0577691 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244769 | TTAAAAAAAAAAAAA[-/AACTT]AACTTTAAAAATTCT | 56916 |
rs201689939 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238025 | AAGTGGATTCTTACT[A/G]CTATTAATTTTTTCG | 56916 |
rs201690975 | snp | C/G | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94274774 | ATTTATGGTGCCCTA[C/G]TTTGAAGGTCCTCTG | 56916 |
rs201743642 | in-del | -/TTA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247115 | GACTGTAGTAATTGC[-/TTA]TTATTGTTTTGATTG | 56916 |
rs201820971 | snp | A/G | 8.24042e-05 | 0.00641836 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277174 | AGTAAGCATAAATGC[A/G]TATTTTCTCCCAAAT | 56916 |
rs201830310 | in-del | -/TAGA | 0.00874735 | 0.0655527 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94209885 | TGTTTCCTCTGTAGT[-/TAGA]TAGTTCAGGAAAGCC | 56916 |
rs201835005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94278909 | GTTTTATTTTTTACT[A/G]TGTTCTCTTTGAGTC | 56916 |
rs201845442 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94284972 | TAGAGAAGTACTAGT[C/T]ATAAAACTAATAAGC | 56916 |
rs201853859 | snp | A/G | 5.19314e-05 | 0.00509539 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94273709 | CGTTGTTCCAGCTTC[A/G]ACTATAGGTTTGTAA | 56916 |
rs201870111 | snp | A/G | 3.29821e-05 | 0.00406078 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281443 | AAAACGATTTTTTCT[A/G]TTTCTAATTCATGTA | 56916 |
rs201895839 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214366 | TCTCGGGTTCATGCC[A/G]TTCTTCTGCTTCAGC | 56916 |
rs202087515 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262908 | AAAAAAAAAAAAAAA[A/G]AAAGAAAAGAAATGG | 56916 |
rs202091751 | in-del | -/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277381 | AGTCTTGGTTAATAT[-/C]CCTAATTTTCTGAAG | 56916 |
rs202111891 | snp | C/T | 1.65616e-05 | 0.00287759 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226310 | GTGTAAGCTGATTAA[C/T]AGATATATTGTATTT | 56916 |
rs202115848 | snp | A/G | 1.6476e-05 | 0.00287014 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94277159 | GTTTTCCTCTAAGAC[A/G]GTAAGCATAAATGCA | 56916 |
rs202126150 | in-del | -/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239378 | AAATTGCAGTCTTAA[-/C]AGACAGTATCATCCT | 56916 |
rs202131764 | snp | C/T | 6.9006e-05 | 0.00587352 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276497 | AATGTTTGTAAAGTT[C/T]TCCAAATTACTGTAA | 56916 |
rs202137103 | snp | A/C | 0.00199798 | 0.0315436 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280803 | AAAAGAATGGCGTTT[A/C]TTTTGTATTTTCTCA | 56916 |
rs202158892 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226382 | TGAGATATTTTGGTG[A/T]CTTCCCTTTTTTTTT | 56916 |
rs202175007 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277752 | TTCCACATCACTAAT[C/G]TTTTGCAAGAATTTT | 56916 |
rs202192992 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285616 | ACACTGTTATGTCTG[G/T]GTTATATTAGGCACT | 56916 |
rs202225770 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240216 | TTCTCTGAAAGCAAA[A/G]GTATTTAAGAAGTAG | 56916 |
rs207464894 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233617 | AACTTCGTCTGACAT[A/G]GAGAGTATTGGTGAA | 56916 |
rs267600302 | snp | A/T | | | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94281527 | TGGATATCTTAGAGG[A/T]TCTATTAAAACATCA | 56916 |
rs367553922 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216397 | CTGCATTCCGCATTA[A/C]CACACTATAAATATA | 56916 |
rs367567384 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270995 | ACCCTCCTCACTCCT[C/T]CCCAAGATGAAGATA | 56916 |
rs367569271 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232054 | TTTTAGTGGAGATGG[C/G]GTTTCACCATGTTAG | 56916 |
rs367614432 | in-del | -/T | 0.00795532 | 0.062565 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289415 | AAATAATTGAGACAA[-/T]TTTTTTTTTAAGTAA | 56916 |
rs367643014 | snp | A/C | 3.29968e-05 | 0.00406169 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208571 | TCCTGATTCAGATAT[A/C]ACTGAAAAAACAGGT | 56916 |
rs367650164 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215952 | ATATCTTAAATTCCA[C/T]GTGTCTTAGTCTGTT | 56916 |
rs367695641 | in-del | -/CATA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281166 | TCCAGATAATACATA[-/CATA]AGCAGTTGTCCACAT | 56916 |
rs367695955 | snp | A/G | 0.0248432 | 0.108648 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291184 | TCTTTTTTTGTTGTT[A/G]TTGTTGTTGTTGTTA | 56916 |
rs367703372 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281792 | TTGGGAGGCTGATGC[A/G]GGCGGATTGGTTGGG | 56916 |
rs367710018 | snp | C/T | 0.000148389 | 0.00861234 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252824 | TTCAGGTTCTGATGT[C/T]GGTAGTTCACTAGAT | 56916 |
rs367775203 | snp | A/C/G | 3.29724e-05 | 0.00406021 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289554 | AGAACTGTGAACTCT[A/C/G]AATTGATGAGGAAAT | 56916 |
rs367868224 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257231 | TATCATTTTTTGAGA[A/C]TGATTTGTTTTACCT | 56916 |
rs367904610 | snp | A/G | 7.67941e-05 | 0.00619606 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264949 | ATGGCACATAAGTG[A/G] | 56916 |
rs367991532 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211101 | AACATGGAGAAACCC[C/T]GTTTCTACTAAAAAT | 56916 |
rs368017848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225443 | CATAATAATTTTGAG[A/G]GTACAATCTCCAAAT | 56916 |
rs368026206 | in-del | -/AAA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262889 | ACAGTAATTTCTGTT[-/AAA]AAAAAAAAAAAAAAA | 56916 |
rs368064876 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288088 | TTTGTTTTTTCTACT[A/T]CTTTTTTCCCATTGA | 56916 |
rs368068948 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244765 | AACATTAAAAAAAAA[A/C]AAAAACTTAACTTTA | 56916 |
rs368076324 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256785 | TTTATTTGTAAGATT[A/G]CTATATATTCAGGCT | 56916 |
rs368082182 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212946 | CCTCTGCCCCCTGAT[A/C/T]TATTTTACTCTTCTC | 56916 |
rs368082491 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256724 | TTGGCCACTTAAAGC[-/A]TGGTAATACATATTT | 56916 |
rs368128439 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272580 | TTTCTGGTTATGTAG[G/T]ATATGCAGTATACTC | 56916 |
rs368167302 | snp | G/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94281576 | ATTAGATGGAAAGAC[G/T]CAGATTTCTGAAAGG | 56916 |
rs368236725 | snp | C/T | 5.04689e-05 | 0.00502314 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264695 | TCAATTATTTTTCTT[C/T]TTATGCTATAGTTCA | 56916 |
rs368316506 | snp | A/G | 6.62471e-05 | 0.00575492 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280799 | TTAAAAAAGAATGGC[A/G]TTTCTTTTGTATTTT | 56916 |
rs368352667 | in-del | -/GTATGTAT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240085 | TAAGCTGACATGTAT[-/GTATGTAT]TTGAGCTGCATAGTT | 56916 |
rs368352698 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250050 | CATCTGTAACCCTGC[C/T]CCCATCAAGTAACTG | 56916 |
rs368460484 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213313 | TATGACCTTTGGAGT[A/G]GACTCTAAACAATGA | 56916 |
rs368466127 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272045 | CAGTCCAAGATGAGT[G/T]TATCGGTAGCTTGCG | 56916 |
rs368548941 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229700 | GCTGGTGAGGTAGGA[A/G]TTAATGTCATTGCCC | 56916 |
rs368603057 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289602 | AAGGACATTTACATT[A/G]TGATGACCATGGGGT | 56916 |
rs368658261 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279302 | CAGGCACGCACCACC[A/G]TGCCCGGCTAATTTT | 56916 |
rs368738511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262655 | GACATGTGAATTTAT[C/T]TTTCCATTAAAACAG | 56916 |
rs368768764 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217202 | AATTTTATTTCATTA[C/T]AGGGACTAAAGAAAG | 56916 |
rs368773948 | in-del | -/CTTA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226555 | TTTTGAGAGCAGATA[-/CTTA]ATTTCCTTATTATGG | 56916 |
rs368781018 | in-del | -/C | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269759 | CTATAACTTCTGCCT[-/C]CCAGGCTCAGGTGAT | 56916 |
rs368809274 | snp | A/G | 4.95119e-05 | 0.00497529 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226241 | GATGTCGTTTCCCCA[A/G]ATTGCTCCAATACAG | 56916 |
rs368945290 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235668 | TTTTTTTTGTGGAAA[A/C]AAATGTAGACATGAG | 56916 |
rs368994420 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239372 | AACCACAAATTGCAG[A/T]CTTAACAGACAGTAT | 56916 |
rs369063442 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218938 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGATTACA | 56916 |
rs369122348 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259094 | AGCCTCCCTTGTGAT[C/T]GTTTGACAAAGTTCA | 56916 |
rs369130807 | snp | G/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207878 | CCGCGTCAACTTCCG[G/T]GCGGATGCCCGCCAG | 56916 |
rs369149172 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237026 | TGATGCAGGTATGCT[G/T]GACTTAATTTTAAGC | 56916 |
rs369172332 | snp | A/G | 6.61332e-05 | 0.00574998 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94264861 | CCATGCTTACTGGAA[A/G]TGGAGGTGGATGGAA | 56916 |
rs369198876 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258397 | TGACCTCAAGTGATC[C/T]GCTCACCTCCACCTC | 56916 |
rs369241783 | snp | C/T | 0.0279179 | 0.114802 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290549 | ACTCTTATCAAAATA[C/T]ATTTTACCAGTTTCC | 56916 |
rs369255576 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240235 | TTTAAGAAGTAGGTA[A/G]ATATATACATAATGT | 56916 |
rs369454887 | snp | C/T | 2.4261e-05 | 0.0034828 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252646 | CACAAAGTGAGGTTC[C/T]AAATGGAAAAGAAGT | 56916 |
rs369463405 | snp | C/T | 8.39426e-05 | 0.00647798 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94253030 | TTTATTCTTTTTTTC[C/T]CCTTGTATGTGTGTG | 56916 |
rs369483731 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256643 | GCCGGGGTTACAGGC[A/G]TGAGCCACTGCATCT | 56916 |
rs369490471 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226885 | TTTTTCTTGTTTTTT[C/T]TAGAGGTGGGGTCTT | 56916 |
rs369516918 | snp | C/G | 3.29679e-05 | 0.00405991 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270717 | ATATTTGGTAACTCT[C/G]TCTTTACCAGTTTGT | 56916 |
rs369550870 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213544 | TATTTGGTACACATC[A/G]TAGAGCATTTCATTA | 56916 |
rs369563295 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226606 | TTAGTACCTTTGATC[A/G]TGTATAACTGCTTTA | 56916 |
rs369573286 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262574 | AGTTCAGTTTAGAAC[A/G]CATTAAAATGATTCA | 56916 |
rs369616354 | in-del | -/ATC | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94251170 | CTTGTGATTGGTGAT[-/ATC]ATGTCATTACTGTAA | 56916 |
rs369623665 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234559 | AGTCCTGCCAGTAGC[A/G]CTCTTGCTGAGAAAT | 56916 |
rs369631512 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275921 | TCCTGCCTCAGCCTC[C/G]TGAATAGCTGGGACT | 56916 |
rs369651132 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94234019 | GTAGAAATGATGATA[C/T]TTCAGAACTGGAAGA | 56916 |
rs369659360 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269493 | CTCAGGCAAATTAAG[-/T]TTTTTTTTTTTTTTT | 56916 |
rs369747394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252432 | TATCACCTGCTTTTG[A/G]AACAATTGTTTAACT | 56916 |
rs369764432 | snp | A/G | 6.61201e-05 | 0.00574941 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237048 | ATTTTAAGCCATGTC[A/G]ATTTATTGTTACGTC | 56916 |
rs369832691 | snp | C/T | 0.000106496 | 0.00729635 | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94278888 | ATTTCAACAGTTATC[C/T]GCTTGGTTTTATTTT | 56916 |
rs369859238 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280332 | TATACCCCAGACTTC[A/T]CCCCAGGGTTATTTT | 56916 |
rs369862228 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214711 | GACATATTTTCCCTG[G/T]GGGGGATAATTGAAG | 56916 |
rs369866384 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216280 | AACATACCGTTTTGG[A/G]GAGTGGGGCACAAAC | 56916 |
rs369873703 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267387 | TTACGGGACATAAAC[C/T]TTTGGTCGGACAGCA | 56916 |
rs369896117 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231575 | TGTTTATTGTGTCAC[C/G]TATTATTATTTTTAG | 56916 |
rs369902455 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248300 | TGATATTCCATTTTA[C/T]GTGTTTACCACAATT | 56916 |
rs369919158 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269949 | AAGTGCTGGGATTAC[A/G]GGCATGAGCCACTGT | 56916 |
rs370104013 | snp | A/C | | | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94251353 | ATGTTTAGTAACATA[A/C]CTAAGGAAGAATCAA | 56916 |
rs370120773 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223979 | TTTAATACAGTAAAG[A/T]TCTAAATTTTTAGTT | 56916 |
rs370274179 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243549 | TGTCAAGTCAATAGC[C/T]GTTTCACAAAAATAC | 56916 |
rs370276619 | in-del | -/AGTT | | | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209425 | ATAAACTAATTAGTT[-/AGTT]TCTTAGGAAAGGTGA | 56916 |
rs370312897 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262133 | CTTTGATGGTCACCT[C/G]TGTGGCATCTTTTTC | 56916 |
rs370363007 | snp | A/C | 6.59163e-05 | 0.00574054 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94274758 | TGGTTAAGGGAAGTT[A/C]ATTTATGGTGCCCTA | 56916 |
rs370374878 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256842 | GTTTGTATTAAAAAA[-/A]ATCTGCAAGTACATT | 56916 |
rs370384380 | in-del | -/T | 0.0138799 | 0.0821421 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237546 | ACTACTAAAAAAGTA[-/T]TTAAATAGTGAAAGC | 56916 |
rs370388938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278074 | ATTTTCTACCCCCCA[C/T]GCTCCTCCTTACCCA | 56916 |
rs370394907 | snp | A/G | 5.05165e-05 | 0.00502551 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276305 | CAAGCTCTTAAAGGT[A/G]TAACCTTAGAGATGT | 56916 |
rs370397347 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275811 | CTTTTTTTTTTTTTT[A/T]TTTGAGACGGAGTCT | 56916 |
rs370422097 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243166 | CTGATCTCAAACTCC[C/T]GACCTCAGGTGATCC | 56916 |
rs370620105 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215992 | GTAACTACCATGAAC[C/T]GGGTAGCTTATAAGC | 56916 |
rs370657475 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269803 | TCTCCTGAGTAGCTG[A/G]GACTACAAGCATACG | 56916 |
rs370780856 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94209776 | GGAACAACTGAAGGA[C/T]TTTAAGCACCAGGAT | 56916 |
rs370829707 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268316 | TATTTTGACAGTTAA[A/G]TAGACTCTTTTCCCA | 56916 |
rs370832123 | snp | A/G | 1.65113e-05 | 0.00287322 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94249667 | AGGGAGAGGAATCAA[A/G]TGAGTCTGCAGAATC | 56916 |
rs370869861 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242567 | ATATTATAGCAGTTG[G/T]TCACTTGGCTGGTTC | 56916 |
rs370884075 | in-del | -/AAAAT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234159 | AGCTGTAATGATGAT[-/AAAAT]CTCTCCTGCATTCAG | 56916 |
rs370967642 | snp | A/G | 1.697e-05 | 0.00291285 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289434 | TTTTTTAAGTAAAAT[A/G]TTTTTATAAAGCTTT | 56916 |
rs371005501 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247631 | CTGTCTAGTTCCAAA[C/T]GCTGTCATCACCTCG | 56916 |
rs371198232 | snp | A/G | 1.6566e-05 | 0.00287797 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94278721 | AGATTGAAAAAATCT[A/G]TCAATAACTTGGGTA | 56916 |
rs371203611 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272647 | ATGTTATTGAGATCT[A/G]TCTGTGTTCTTATAT | 56916 |
rs371222313 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220048 | TATGGTACTACTTAA[A/G]AGTGCCTATTTGCTT | 56916 |
rs371236900 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274123 | AATAAGAGAATATTT[A/G]TACATGTGAATGTAA | 56916 |
rs371237367 | in-del | -/CG | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284591 | GTTTTTTTTTTTTTT[-/CG]TTTTTTTTTTTAAGT | 56916 |
rs371256313 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274178 | ATTGGAGGTTAATAA[G/T]CAACTGTAAATATAA | 56916 |
rs371260508 | snp | A/G | 7.00464e-05 | 0.00591763 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278386 | CAATAATTTAAGTGA[A/G]TAATTCCTAAAAGGA | 56916 |
rs371285373 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217033 | AGGTGCTCCACCATT[G/T]TACATTTCTGCCAAC | 56916 |
rs371293036 | in-del | -/GA/T | 3.79168e-05 | 0.00435396 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240881 | TTCTGTGCAAAGTTT[-/GA/T]GAGTGTGCTGCTCTG | 56916 |
rs371383357 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288099 | TACTTCTTTTTTCCC[A/G]TTGATCCATAATAAA | 56916 |
rs371409804 | in-del | -/TTC | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258965 | TCTAAAATCAAACTA[-/TTC]TTCTTTTTTTGTTGT | 56916 |
rs371419208 | snp | A/G | | | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94278836 | TTTAAAAAATTATCT[A/G]GAATTTGAGGAAATA | 56916 |
rs371420894 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281825 | CAGGAGTTCAAGACT[A/G]CCCTGGACAACATGA | 56916 |
rs371428287 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260725 | ACTCTAAATGTTGCC[A/G]TTCATATACAAAATT | 56916 |
rs371429966 | in-del | -/CAAAA | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270158 | GTAGCATGTAAGTGT[-/CAAAA]CAAATAATTTTGCTA | 56916 |
rs371482856 | snp | A/G | 1.65789e-05 | 0.0028791 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226164 | ATGAAAGAAAAGCAA[A/G]TATATCATATTTCAA | 56916 |
rs371485186 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256862 | GCAAGTACATTTTGA[A/G]TACTTTGTAGGCTGC | 56916 |
rs371524829 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255945 | GGGTTCAGAAATACA[G/T]CAAGCCAAAAATGTC | 56916 |
rs371532942 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231306 | AAGATTCAGGAGAAA[C/G]ATAGTAGATAGTTAG | 56916 |
rs371561977 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244891 | AACAGCCCCTTTTTA[A/G]GTGTGTGACAGCAGT | 56916 |
rs371571493 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257840 | GTAGGTCTTATCTAT[C/G]AACTTAATATTATAG | 56916 |
rs371580989 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281275 | CTGAAGTTAAGGCAG[C/T]TTATTCATATATAGG | 56916 |
rs371660055 | snp | G/T | 4.35977e-05 | 0.00466872 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283096 | ACTTTTTAGTGAGAT[G/T]TAACCTAATTTGTTT | 56916 |
rs371811988 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259085 | AACTGTTTTAGCCTC[C/G]CTTGTGATCGTTTGA | 56916 |
rs371817279 | in-del | -/ATT | | | utr-variant-3-prime, nc-transcript-variant, cds-indel, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291184 | TCTTTTTTTGTTGTT[-/ATT]GTTGTTGTTGTTATA | 56916 |
rs371988225 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279308 | CGCACCACCATGCCC[A/G]GCTAATTTTTTTGTA | 56916 |
rs371990495 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239934 | GGCAAGATTATCTGG[A/T]TTGAAGGTTTTTTTC | 56916 |
rs372060179 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268728 | CTTAACTTCTGTGAG[A/C]CGCAGTGAACTTCTC | 56916 |
rs372060663 | snp | C/T | 1.66966e-05 | 0.00288929 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280580 | GTATACTGTGTTTTG[C/T]TTTGTTTTAAGGAAC | 56916 |
rs372092554 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272426 | TAAAATGTACAAATA[C/T]ACAGCTTAGTGACTT | 56916 |
rs372101939 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217485 | TGAAAGTTGTTTAGA[A/G]GCCATTTTTATGAGG | 56916 |
rs372120816 | snp | A/G | 3.31934e-05 | 0.00407377 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94264886 | ATGGAACATAGAACA[A/G]CCTTCCATTCTAAAC | 56916 |
rs372260378 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288999 | TAATCATCAGCTGGT[A/G]TGCTGTGCTCAGAAT | 56916 |
rs372339224 | in-del | -/GTA | 0.00478085 | 0.0486577 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94209605 | CCCTTCTACTTAAAT[-/GTA]ATAATGATGGCAGAT | 56916 |
rs372341021 | snp | C/T | 0.000176704 | 0.00939793 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252619 | TTTTATATACAGATA[C/T]GCAATATGTATCACA | 56916 |
rs372355022 | snp | A/T | 0.000620071 | 0.0175969 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280544 | TTTTCTCATCATATT[A/T]TTAATTATTTTTATT | 56916 |
rs372371945 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264039 | GTTTTCACAGAGAAC[A/C]ATTTATAGTATTATA | 56916 |
rs372416652 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94263124 | CGAGGATTTAATGAG[C/T]TACTGAATAAAAGGT | 56916 |
rs372437348 | in-del | -/TTA | 0.00755907 | 0.0610114 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285948 | TGGGCAATGTTTTCC[-/TTA]TTATTTTGGTAGGGC | 56916 |
rs372439025 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289878 | TCTACCTCCAAATAT[A/G]TATATATTGTCTTTC | 56916 |
rs372518795 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219829 | CATGGCTACTTCACT[C/G]CTATTTCAAAAGGGC | 56916 |
rs372543319 | in-del | -/A | 0.000957541 | 0.0218599 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276997 | TTAAGAAAAAGCTAA[-/A]TATAAATTTTACCTT | 56916 |
rs372551135 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247781 | GGAATTATATAATAT[A/G]TAACCTTTTATGTCT | 56916 |
rs372555643 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268989 | ATTGGGAAAGCAAAG[A/G]CCTTTTTTAAAATTC | 56916 |
rs372564335 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244019 | CACATTATGGACCAT[C/T]AAAGATAATGCCACA | 56916 |
rs372565503 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262825 | TGTTTCCCAATGTTC[A/G]TAGACCACAAGGACA | 56916 |
rs372578896 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237472 | TTAAATAAATGCTGA[C/T]TCGATTTTTTTTAAC | 56916 |
rs372651872 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285689 | GAGAGAAGTGCGTAT[A/G]ATCAAATAATTACTA | 56916 |
rs372652503 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280340 | AGACTTCTCCCCAGG[A/G]TTATTTTGAACCAAG | 56916 |
rs372654218 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264976 | TGAATTTATTTCTGT[A/G]TCGTGCCTAGAAAGT | 56916 |
rs372657831 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214483 | CGTATTAGCCAGGAT[G/T]GTCTCAATCTCCTGA | 56916 |
rs372703050 | snp | A/G | 1.65255e-05 | 0.00287445 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237043 | ACTTAATTTTAAGCC[A/G]TGTCGATTTATTGTT | 56916 |
rs372823947 | snp | A/G | 1.66551e-05 | 0.00288571 | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94279067 | TAAGGATTTCATATT[A/G]TGTTAACACTAAGCT | 56916 |
rs372854144 | in-del | -/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226414 | TTCTTTTTTTTTTTT[-/T]GCCCCACCTGCCTTT | 56916 |
rs372863791 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249317 | CTTTTAAAATTTACC[A/G]TTGTCTTGGAGAAGG | 56916 |
rs372930619 | snp | C/G | 0.000542999 | 0.0164683 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234164 | TAATGATGATAAAAT[C/G]TCTCCTGCATTCAGT | 56916 |
rs373015689 | snp | C/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207916 | TCCGCCGCTCCCCTT[C/T]TTTGGCCCCTTTGTG | 56916 |
rs373034529 | snp | A/G | 0.000115336 | 0.00759305 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94280695 | AGTACCGACACATTA[A/G]TAACTTTCAGTTAGA | 56916 |
rs373127175 | snp | C/T | 5.14434e-05 | 0.0050714 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226111 | TTCTCCTTTTTATTC[C/T]CTTGCAGAAGATTCT | 56916 |
rs373146831 | snp | A/C | | | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291367 | CATATAATATTGGGC[A/C]CAAATGAGATTATCT | 56916 |
rs373161528 | in-del | -/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275796 | TAACATTAACATTTT[-/C]TTTTTTTTTTTTTTT | 56916 |
rs373172532 | snp | A/G | 2.06639e-05 | 0.00321427 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283104 | GTGAGATTTAACCTA[A/G]TTTGTTTATCTTACA | 56916 |
rs373192381 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260662 | ATTTTAATACTGTTA[C/T]TGCTGCTTGTTGAGG | 56916 |
rs373200820 | snp | A/C | | | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208879 | TTGGAAGAGCGATGT[A/C]AGTGATTCAGTCCTA | 56916 |
rs373212379 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275891 | AACCTCTTGCCTCCC[A/G]GGTTCACGCCATTCT | 56916 |
rs373213691 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265403 | CCTTTTGGGGTAGAA[A/T]TACATCAGCAAGGGA | 56916 |
rs373304622 | snp | A/G | 0.000118238 | 0.00768799 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276525 | TAAAATTTAGATTAC[A/G]TAATTTAATATATGT | 56916 |
rs373371234 | snp | A/G | 0.000187213 | 0.00967324 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291002 | GAACAGACTGAATAT[A/G]TTTTACCATTACAGG | 56916 |
rs373400914 | snp | C/G | 0.000208572 | 0.0102099 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264919 | AAGGTAATCTTTGTT[C/G]AATATATTTATTCGT | 56916 |
rs373402914 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215236 | TAATTGAAAAGCAAT[A/G]CTTAGTTAAAGGGTT | 56916 |
rs373423601 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240526 | ACTCAGAAATTGCTG[A/G]TTTCTGTGATGGTAT | 56916 |
rs373448486 | in-del | -/AG | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232964 | CAGTCTGGGTGACAG[-/AG]TGGAACCCCGTCTCA | 56916 |
rs373507176 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258469 | CCTCTGGTAATCTGT[C/T]AGTTTCATCTCTTTT | 56916 |
rs373514021 | snp | A/G | 0.000160685 | 0.00896194 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240865 | AATTGATTTTTTGCT[A/G]TTTCTGTGCAAAGTT | 56916 |
rs373519542 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222728 | AACATTTCAGGAGGC[C/T]GAGGCAGGTGGATCA | 56916 |
rs373571416 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215919 | AATACATGTCTCTCC[A/G]ATAAATTATTTGTAA | 56916 |
rs373573803 | snp | C/T | 3.30518e-05 | 0.00406507 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252799 | GAGTTGTTGAAGACT[C/T]TGAATATGATTCAGG | 56916 |
rs373660660 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273577 | GTATTTATTTTTTGT[C/T]TGTTTTAAAATGTTA | 56916 |
rs373665442 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94253764 | AGTTTTATGAATGCC[A/T]ACAGTCATCAAATCT | 56916 |
rs373692984 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231644 | CCCTTAATACTGGTT[A/G]TGTATCTGCCATCTA | 56916 |
rs373695530 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246285 | CCACCACGCCTGGCT[A/G]ATTTTTTGTATTTTT | 56916 |
rs373714817 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238966 | TCATAAGAGTTTACA[A/G]TCATTAAATTTATTT | 56916 |
rs373736346 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289074 | CTTTAGATGAAAAAT[A/T]AGAATATAGATTGGT | 56916 |
rs373757304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256936 | CAGGGCTGTCTTTTG[A/G]TAAGTGGGGATTTAA | 56916 |
rs373829337 | in-del | -/TTATTTTATTTTATTTTA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275798 | CATTAACATTTTCTT[-/TTATTTTATTTTATTTTA]TTTTTTTTTTTTTTT | 56916 |
rs373916469 | snp | C/T | 0.000164951 | 0.00908011 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277191 | ATTTTCTCCCAAATA[C/T]GTTATTTGTGTTTTA | 56916 |
rs373944812 | snp | C/T | 1.65864e-05 | 0.00287974 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94250820 | ATCTCTAAAAGTGTT[C/T]GCAGAAGACCAAGGT | 56916 |
rs373946249 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246979 | GTAAAGCAGCTGCAG[A/C]TGGAGTTTGATTGTT | 56916 |
rs373949338 | in-del | -/GT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267760 | ATATTTTAATACTCT[-/GT]TGAGAAGAAAGCACT | 56916 |
rs374018687 | in-del | -/CTT | 0.000613779 | 0.0175075 | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208187 | GATACCCCCGTCCAC[-/CTT]CTAATTGTTGCGGCC | 56916 |
rs374042903 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247807 | TGTCTAGCCTCTTAT[G/T]TTTTAATTTCAGAAA | 56916 |
rs374058320 | snp | C/G | 3.29462e-05 | 0.00405857 | missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208506 | TCTTCACCAATTTCT[C/G]TTAGTGCTGAAGAGG | 56916 |
rs374109918 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210463 | AGAAAGTTTTAAAAG[C/T]CAGTTTAGCAGTAGT | 56916 |
rs374136108 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227957 | AACTCTGGATTTTTA[G/T]AATCAGGGAGATGAG | 56916 |
rs374187539 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286045 | ATGGATTTTATTCTA[A/G]CAAGTTTCTAAATAT | 56916 |
rs374191239 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256843 | TTTGTATTAAAAAAA[-/A]TCTGCAAGTACATTT | 56916 |
rs374197618 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262404 | AGATCGTGAATCTTA[C/T]CAGTTTCTCCGTGTC | 56916 |
rs374236471 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230453 | GTGTGAACATTCCTT[A/G]TTTTATTCATTCATT | 56916 |
rs374240816 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256740 | TGGTAATACATATTT[C/T]TTCCTTCTGAATAAG | 56916 |
rs374285057 | snp | G/T | | | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94279211 | TTGCCAAGGCAGGCA[G/T]TCTGGGCTCACTGCA | 56916 |
rs374292191 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224213 | TATAAAATTGTTCTT[C/T]TGGAAAAAAGTATGA | 56916 |
rs374339586 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281113 | TTAAGTAATGCTGCC[A/G]TTTATGTGTGAAATA | 56916 |
rs374358540 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243181 | TGACCTCAGGTGATC[C/T]GCCTGCTTTGGCCTC | 56916 |
rs374413095 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225880 | TTAGAATATAAAACA[C/G]AAACCTATGTTATTT | 56916 |
rs374425077 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261822 | GCCATGTTGCCCAGG[C/T]GGGTCTTGAAATCCT | 56916 |
rs374576192 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222833 | GCCGGGTGTCGGGGC[A/T]GGCACCTGTAATCCC | 56916 |
rs374589263 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211791 | TGCTGATATTTGCAT[A/G]TGACTCAGATGCTTT | 56916 |
rs374599295 | in-del | -/ACT | | | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208966 | AAATATTGATCATCT[-/ACT]GTGAGCTAGACATTG | 56916 |
rs374600779 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260755 | TCAGAATAAATGTTT[A/T]TTCTTTCCTTTAATT | 56916 |
rs374649720 | snp | A/G | 1.66037e-05 | 0.00288125 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289457 | AAAGCTTTTAATGCT[A/G]CTTTCTGACCTACAG | 56916 |
rs374724305 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256037 | ACACATTTGATGGCA[A/T]CAGTTCACCATCCAC | 56916 |
rs374759242 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245081 | GCAGAAAATTGCCTT[G/T]GACTTGATTCTTTAT | 56916 |
rs374785392 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212555 | GCAGTGGCACAATCT[C/T]GGCTCACTGCAACCT | 56916 |
rs374791340 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278167 | GACTTCTGAACACCC[A/G]TCTGGTACAGTTCAA | 56916 |
rs374802228 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223846 | TCGGCCTCCCAAAGT[C/T]CTGGGATTATAGGTG | 56916 |
rs374849578 | snp | A/T | 1.66065e-05 | 0.00288149 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94274954 | TGAAGATTACAATGT[A/T]ATTGTGACCACGTAA | 56916 |
rs374904067 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232156 | GTGTGAGCCACTGCA[C/G]CCGGCTGGTTTTTCT | 56916 |
rs374908092 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218969 | GATGTGCACCACCAC[A/G]CCTGGCTAATTTTTG | 56916 |
rs374909281 | snp | C/T | 0.391397 | 0.206172 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246133 | TTTTTTTTTTTTTTT[C/T]TTTTGAGATGGAGTC | 56916 |
rs374969985 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211930 | TTCTTCATAGTATTT[-/T]ATCACTAGCTAACCT | 56916 |
rs374994929 | in-del | -/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264626 | AAATTAGCAAACTTG[-/G]TTTTCCTCATAAAGA | 56916 |
rs375171618 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248231 | TTCAGATATACTACA[A/G]TGTTCATTCATGTTG | 56916 |
rs375226879 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273436 | AGTTATAGCATCATT[G/T]GGAGATTATAATCAA | 56916 |
rs375233163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233114 | TGCATATTCTAGATA[C/T]GTGTCTAAGAGAGCT | 56916 |
rs375323927 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269223 | CACTCAGTTCTAATT[A/G]TGTCTTGATTTCAGA | 56916 |
rs375341191 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264431 | TAAGAGAATAGCTGC[C/T]AGGGTCAAAGTAACA | 56916 |
rs375345716 | snp | A/G | 1.64977e-05 | 0.00287203 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94236985 | ACTATGGATGGAGCA[A/G]TTGCTGCTGCCTTGC | 56916 |
rs375386368 | snp | A/C/G | 0.00018202 | 0.00953828 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276981 | ATGAAAGGAGTGGCT[A/C/G]TTTAAGAAAAAGCTA | 56916 |
rs375438190 | snp | A/G | 5.04825e-05 | 0.00502381 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289442 | GTAAAATATTTTTAT[A/G]AAGCTTTTAATGCTA | 56916 |
rs375467421 | snp | A/G/T | 3.31654e-05 | 0.00407208 | synonymous-codon, missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94278624 | GTCTCAGGTTCTCAA[A/G/T]CAGTTACCCCCCAAG | 56916 |
rs375528450 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274699 | ATGTGAACATACCCT[A/G]TTGTAGCAGATGCAA | 56916 |
rs375539863 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255752 | AATTTGATTTTTTTT[A/G]AAGTATATTACCTAA | 56916 |
rs375567340 | snp | C/T | 1.65583e-05 | 0.00287731 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280798 | ATTAAAAAAGAATGG[C/T]GTTTCTTTTGTATTT | 56916 |
rs375640893 | snp | A/T | 1.66499e-05 | 0.00288525 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278567 | TTTTTAAAACTTAGG[A/T]TTTTCTCTTTACTAG | 56916 |
rs375673291 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229883 | TCTTTGCCTCTCATT[C/G]TGTTTTCTTCTGACA | 56916 |
rs375772724 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267188 | CATCCTGAACTTGAC[A/G]GCATGGTTCCTACCC | 56916 |
rs375820099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280924 | GAACATTTTCTTGAC[A/G]TATTTTCTTGATTAC | 56916 |
rs375909174 | in-del | -/ATG | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243408 | CATTTCTACTTGATG[-/ATG]GGTTGCTGCTGCCAA | 56916 |
rs375955649 | in-del | -/TTTTTTTTA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223753 | TTTTTTTTTTTTTTT[-/TTTTTTTTA]AAGTAGAGACGAGGT | 56916 |
rs376015184 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275841 | TCACTCTGTCCCCCA[A/G]GCTAGAGTGCAGTGG | 56916 |
rs376036485 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230694 | AGCAAAACTACCCCC[-/T]ACCCCAACTTTGAGA | 56916 |
rs376036975 | snp | A/T | 1.66275e-05 | 0.00288331 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236920 | TTCTTAAAGTGCTGA[A/T]TTAAAACATTAATCT | 56916 |
rs376060629 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276296 | ACTAGACTCCAAGCT[C/G]TTAAAGGTATAACCT | 56916 |
rs376099012 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94264729 | AGATGTCCAAAACTA[A/G]TGGCTTATCAGAAGA | 56916 |
rs376108327 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235545 | TTTCCACCCAGATCA[C/T]TTTGATACCATCTTA | 56916 |
rs376119878 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209490 | ATTTCAGTAATATCT[A/T]TTTTTATGCAAAACT | 56916 |
rs376130325 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260901 | AATAAATAAAAAGAC[A/G]TCAAACTTAAATGTG | 56916 |
rs376150132 | snp | A/C | 3.7262e-05 | 0.0043162 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241023 | TAAGTTTACATTTGA[A/C]TTACAGTATCAAAAT | 56916 |
rs376182003 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211966 | TATGTAGTTGTGTAT[A/C]ACTAGCTAACATTAC | 56916 |
rs376232785 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239941 | TTATCTGGTTTGAAG[G/T]TTTTTTTCAGACTTA | 56916 |
rs376239868 | in-del | -/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226402 | CCTTTTTTTTTTTTT[-/C]TTTTTTTTTTTTGCC | 56916 |
rs376273653 | in-del | -/GTAA | | | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94251683 | TAGCTTTCTGAGTAA[-/GTAA]AAATTTCTGAATAAA | 56916 |
rs376335854 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239337 | GAAACAATGGGAACT[A/G]TCACAATTTCTGGAT | 56916 |
rs376350901 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217819 | TTTCTTGGGTCCTGA[C/G]TAAATATGTATAACT | 56916 |
rs376354117 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243891 | GGTTCAAAAATGCCA[C/T]ACAGTACATGCAGAG | 56916 |
rs376432032 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268042 | AGAAAGGATCTGTAA[C/T]TGGCAGCAGTTCCGT | 56916 |
rs376489179 | snp | A/G | 9.92014e-05 | 0.00704208 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270683 | ACTAATAGAAAACTG[A/G]TAGAAATATAGATGT | 56916 |
rs376536310 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215325 | AAGTGCATTTTAAAT[A/G]TGCATGTATTTGGCT | 56916 |
rs376546580 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230230 | TTCTGTCCCTTCTCC[A/C]TTCAAACCTTAGAAC | 56916 |
rs376560114 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269370 | GCATGGCCTTGTCCT[A/G]TGTTTTCACATTAAT | 56916 |
rs376603896 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218872 | GCTGGAGTGTGGTGG[G/T]GGGATCATGGCTCAC | 56916 |
rs376607169 | snp | C/T | 1.66247e-05 | 0.00288307 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276330 | AGATGTTTTTTCTTT[C/T]GGTGACAGATATAAC | 56916 |
rs376705653 | snp | A/G | | | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252431 | TTATCACCTGCTTTT[A/G]AAACAATTGTTTAAC | 56916 |
rs376715102 | snp | A/G | 1.65042e-05 | 0.0028726 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226229 | TCTGATAGTGAAGAT[A/G]TCGTTTCCCCAAATT | 56916 |
rs376753226 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258042 | TTTATTTTTTTCTCA[-/T]TTTTTTTCCTAGTTG | 56916 |
rs376793612 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289035 | TTATATGTATACAGT[A/G]TGGGTCTGAGTCAGT | 56916 |
rs376831808 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290541 | AACTTGAAACTCTTA[C/T]CAAAATATATTTTAC | 56916 |
rs376864973 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228973 | TAGGTTAAGTGGAAA[A/G]ACTACTACATACTAC | 56916 |
rs376910298 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285337 | AGACGCCTCCTAGTC[A/G]CCCCATCTCCCAACT | 56916 |
rs376956329 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230323 | AAGATAGCATACTAC[A/G]TGTGTGTATATTCAT | 56916 |
rs376969302 | snp | A/G | 1.65954e-05 | 0.00288053 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94233969 | TTCTGAGCCATCTGA[A/G]GATGAAGAGTCCCAA | 56916 |
rs376972473 | in-del | -/TGTTA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283952 | TGGGCTGTCCTGTTA[-/TGTTA]CCCTTTAGGAAGTAA | 56916 |
rs376995554 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223918 | CAGAAAGTAGGACTT[G/T]ATTGTTAAAGTGTTC | 56916 |
rs377000534 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206502 | AGGCTGGGAAGGGTA[G/T]TGTGGGGCGGGGGAG | 56916 |
rs377014080 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289930 | TTTACATGTGCCTTA[C/T]TTGACAATGCTTATG | 56916 |
rs377015910 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232724 | TTGGAAGGCCAAGGC[A/G]GGCGGATCGCTTGAG | 56916 |
rs377021984 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258175 | TTCTTTTCCTTCTTT[C/T]AGACAGTCTTGCCCT | 56916 |
rs377038246 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260025 | AATCTGTAGATTCCT[C/T]ATCCCTCTCTCTCTC | 56916 |
rs377086179 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212962 | TATTTTACTCTTCTC[A/G]GTGCCCAAAGTTGTC | 56916 |
rs377091030 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94263399 | TCCCCTGAAAAGCAC[A/G]AAGTAGGGGGAGTAG | 56916 |
rs377127898 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277995 | TCCCCATTTTTAGAC[C/G]AAGTGATTTGCATCA | 56916 |
rs377131341 | multinucleotide-polymorphism | AA/CT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247365 | AAGTGTCTGTGTAAC[AA/CT]CCTGGACCACATGAG | 56916 |
rs377183953 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249378 | TTTGAGGATCATTCT[A/G]GTTTTTTAGGAGATT | 56916 |
rs377322912 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282801 | AGCCGATATACTTCT[C/G]AGAAGGTTAAAGATT | 56916 |
rs377349843 | snp | C/T | 1.64798e-05 | 0.00287047 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274730 | ATAATGTCTCTTCTG[C/T]TCCATAGATAACTGG | 56916 |
rs377367893 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271311 | TTTATTTTTATTAGC[A/G]GTCTCTCCGGGTCTC | 56916 |
rs377400815 | snp | A/G | 1.64817e-05 | 0.00287064 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94280743 | ATTCTGGAAAATTTC[A/G]AGTTTTAGGATGCAT | 56916 |
rs377525317 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290796 | TATGTAAATATCATT[A/G]TAAATAAACTTATTT | 56916 |
rs377549212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235110 | CATTTAAAATATACA[A/G]TTTTGTGGTTTTTAC | 56916 |
rs377604717 | snp | A/C | 1.64947e-05 | 0.00287177 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94280642 | CTTTGAAGATATGGA[A/C]GTTATGACAGACTTC | 56916 |
rs377607095 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239175 | AGTGCACTTTGAGGT[A/G]GTATATAGAATGACA | 56916 |
rs377693918 | snp | C/T | 9.92835e-05 | 0.00704499 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276982 | TGAAAGGAGTGGCTC[C/T]TTAAGAAAAAGCTAA | 56916 |
rs386400847 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225300 | TTTCCTTGGCTTGTA[-/A]AGGTGATCTCCTTCC | 56916 |
rs386400848 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226408 | TTTTTTTTCTTTTTT[-/T]TTTTTTGCCCCACCT | 56916 |
rs386400849 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226409 | TTTTTTTCTTTTTTT[-/T]TTTTTGCCCCACCTG | 56916 |
rs386400850 | in-del | -/AA | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238931 | TTACATGAGGAAACA[-/AA]GTGGATACAACCTCT | 56916 |
rs386400851 | in-del | -/GTT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247121 | AGTAATTGCTTATTG[-/GTT]TTTTGATTGAGAGGG | 56916 |
rs386677373 | multinucleotide-polymorphism | AG/GT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236089 | TGTGAAATAGTTCTA[AG/GT]CTTGCTAAGAATATG | 56916 |
rs386677375 | in-del | AAATACTGC/TGCT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269081 | AAAAGGCAGAATTAG[AAATACTGC/TGCT]TTTTTCTCCTACCTA | 56916 |
rs386677376 | multinucleotide-polymorphism | CA/TG | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279922 | CAGGCTGGAGTGCGA[CA/TG]GCATGATCTCTGCTC | 56916 |
rs397693311 | in-del | -/TT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239441 | TTGTTTTGAAAGTTT[-/TT]GTTTTTGAATATGAA | 56916 |
rs397699692 | in-del | -/TT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239577 | TTTTTTTTTTTTTTT[-/TT]AATTTTTTATTTTGA | 56916 |
rs397761705 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262946 | TACAGAAAAAAAAAA[-/A]GTGTATTTTGAACTT | 56916 |
rs397772412 | in-del | -/A | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210950 | AAAAAAAAAAAAAAA[-/A]GGTAAATGTCTTTAA | 56916 |
rs397940158 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237511 | CTAAAAAAAAAAAAA[-/A]GTAAAAATCACCTGA | 56916 |
rs397965323 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214440 | TAATTTTTTTTTTTT[-/T]GTATTTTTAGTAGAG | 56916 |
rs397994565 | in-del | -/A | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265403 | CCTTTTGGGGTAGAA[-/A]TACATCAGCAAGGGA | 56916 |
rs398107671 | in-del | -/A | | | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206320 | CGCCATTAAAAAAAA[-/A]TGAGATCCTGTCATT | 56916 |
rs398107672 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225301 | TTCCTTGGCTTGTAA[-/A]GGTGATCTCCTTCCT | 56916 |
rs527259992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236457 | CTATCCCATTTATCT[C/T]GAGCAGTATTAGATT | 56916 |
rs527277519 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94251189 | TGTCATTACTGTAAT[A/G]TAGATGTCTTAGCCT | 56916 |
rs527310849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284609 | TTTTTTTTTTAAGTG[A/G]AGACAGGGTTTTGTC | 56916 |
rs527330069 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243685 | CCATGAGAAATAGTA[G/T]GTGATCATAGAAAAT | 56916 |
rs527424911 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268175 | TAATAAAACCATTTC[A/G]TGTCCTGATCAAAAC | 56916 |
rs527474807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94209908 | TCAGGAAAGCCAAGG[C/T]GTAGACATGGGATTT | 56916 |
rs527480969 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276834 | AGACCAATGGTTTTC[A/G]TATTCATTGCTGTTG | 56916 |
rs527517650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216499 | CCATCTCAACCATTT[C/T]TAAGTGTACAGTTCA | 56916 |
rs527530362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209267 | AATAGTGATAAGTGC[C/T]TCACCTTCTGTCATT | 56916 |
rs527616074 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249001 | ATGAACACAAGGAGT[C/T]TTTTCTTTTTGCTTA | 56916 |
rs527644223 | in-del | -/CTA | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208964 | CAAAATATTGATCAT[-/CTA]CTGTGAGCTAGACAT | 56916 |
rs527721195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250270 | TCATATATAGAAGCA[C/T]ATATTTGTTTAGCAT | 56916 |
rs527805339 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244486 | CATGCCTCGAATAAC[A/C]CAAATATGAAAGACA | 56916 |
rs527807022 | in-del | -/AGT | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236222 | TGATTTAATACAAAA[-/AGT]AGCTTATTTAAAAGT | 56916 |
rs527846584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217449 | TGATGTGTTTTTGTT[A/G]TTGTTGTTTTCTCTT | 56916 |
rs527846646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224428 | TACATAATGAGATTG[A/G]GAATGGAACCCAAGT | 56916 |
rs527855348 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265750 | CAAAACCATGGAAAC[A/T]AATGGAGTTCCTAAA | 56916 |
rs527875743 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218181 | TTATTGTAGGTATAA[A/C]GTCTATTATTTAGAA | 56916 |
rs527879046 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244724 | TTTACTTAGTTCTTC[C/T]CTGTTAAAGAGGATG | 56916 |
rs527925776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231045 | ATTATTGTCCTTAGT[A/G]AGAACAGTTTCACTG | 56916 |
rs527933380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223841 | CCACCTCGGCCTCCC[A/G]AAGTTCTGGGATTAT | 56916 |
rs527935474 | in-del | -/ATAT | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282975 | GGAGGCTCTTCAGTG[-/ATAT]ATATAGCCAGAGGAG | 56916 |
rs527989957 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266767 | AGTTCTTCATGACGA[A/T]GTTTACTTTGCTACA | 56916 |
rs528055833 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241724 | GGAATGGTGCTATAA[C/T]GGGAACTCGTTGGCC | 56916 |
rs528126594 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214459 | TTTTTAGTAGAGACC[C/T]GGTTTCACCGTATTA | 56916 |
rs528162551 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270106 | TCACTGTCTTTTAGC[A/G]TTTGCTAAAACATCA | 56916 |
rs528193693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213234 | AAAGTAGAATCACTA[C/T]CTGTAATTCACAAAT | 56916 |
rs528205904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269267 | ACAATTTATTATACT[A/G]TAGCTATGTCCAGAC | 56916 |
rs528212332 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272725 | GTGGTATGGTAGTCC[A/G]TGGTATAAATACAGT | 56916 |
rs528233688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287777 | CATTTTTTACCTTTT[A/G]GAACTTTAAAAATAT | 56916 |
rs528276435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238718 | TTTTGTAGCTTCCCA[A/G]TACATTCTTGCTCTC | 56916 |
rs528290270 | snp | C/T | 0.00374524 | 0.0431114 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278409 | TAAAAGGATATGTTT[C/T]TATTTTGCTCAGAAA | 56916 |
rs528310621 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287048 | TTTTTGTATTTTTAG[G/T]AGAGACGGGGTTTCA | 56916 |
rs528337926 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238129 | TCATTTTTCTTCCAC[A/T]AAGTGGCCTGTATTC | 56916 |
rs528380723 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275650 | AATAAAATATTAAGT[G/T]TTAAAGAGAAACATG | 56916 |
rs528410406 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282286 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 56916 |
rs528440795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275041 | AATTGTAGTAGTACT[A/G]TGTAGGAAAGTTTAT | 56916 |
rs528443518 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233236 | GATCTCTATAACTTA[A/C]ATTCATTTGTTACTG | 56916 |
rs528481675 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227372 | AATTATCTGAGTTAG[A/G]TGTTTAAAAGGTCTT | 56916 |
rs528490978 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232872 | GTGGTCTCAGCTACT[C/G/T]AGGAGGCTGAGGTGG | 56916 |
rs528505344 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282332 | CGATCTCCTGACCTC[A/G]TGATCCGCCCGCCTC | 56916 |
rs528526091 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238728 | TCCCAATACATTCTT[A/G]CTCTCACATTATCTC | 56916 |
rs528548572 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270340 | ATGTTTGTGTTTTTT[G/T]GTCCTAATACTTTTA | 56916 |
rs528559737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227210 | TTTGAGGAAAGTGGG[A/G]GGGACATGATGCGGA | 56916 |
rs528568208 | snp | A/G | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94277118 | CCACACATGTTTAGT[A/G]GTAGCACCAGTGAAA | 56916 |
rs528675927 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207179 | AGTGAGGAATTACTT[C/T]AAATGCTTTGAAGCT | 56916 |
rs528690395 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287750 | TCCCTTAATGTATTA[A/G]TTGTATTAATACATT | 56916 |
rs528694715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213848 | ACCAAGGTAGTAGAT[A/G]GTTGAATATTAGAGC | 56916 |
rs528746595 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245619 | TTTTCAGATAACCTG[G/T]TTTTTGCCACTTTAC | 56916 |
rs528754759 | snp | C/T | 0.000324675 | 0.012737 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290160 | TTATTTGGCTAGGCA[C/T]TAAGTTGTTTTCCAG | 56916 |
rs528780945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246242 | CTCCCACCTCAGCCT[C/T]CCGAGTAGCTGGGAT | 56916 |
rs528815456 | snp | C/G | 0.000173055 | 0.00930041 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94290968 | ACTCACGGCTTAACC[C/G]CAGTCTTGATGGTAT | 56916 |
rs528862255 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272981 | CCTGGCTAATTTTGT[A/G]TTTTTGTAGAGATGG | 56916 |
rs528868653 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237877 | TATTTATATAGGCTA[A/C]ATTTCAAACTAGGAT | 56916 |
rs528878045 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209016 | CAACCTCTGTACACA[A/G]GGGAAGATCAGATCA | 56916 |
rs528915939 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255532 | TGTTTTCAAGGTAGT[A/G]GACATATAAATGTAA | 56916 |
rs528917268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247462 | ATAGGCACACCATCT[A/G]CTAAATATTTGATTC | 56916 |
rs528948872 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245354 | AATACAAATGATCAG[A/G]TGTTTTAAATGCTGT | 56916 |
rs528955567 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242145 | TTCAAGCAATTCTCG[C/G]ACCTCAGCCTCCGGA | 56916 |
rs529020374 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241733 | CTATAATGGGAACTC[A/G]TTGGCCTCTGTTCCT | 56916 |
rs529024774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270975 | TTTTTGATAGAGTTA[A/G]TTCTACCCTCCTCAC | 56916 |
rs529028578 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261636 | GTTTGTTTTTGAGAC[A/G]GGGTCTCACTCTATC | 56916 |
rs529053917 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214419 | GGTGCCCGCCACCAC[A/G]CCGGGCTAATTTTTT | 56916 |
rs529053985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221535 | TAATTTTTTCACAAA[A/G]TGAAATGAAAACAAT | 56916 |
rs529142575 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220961 | TTGAGCAATTGCTTT[C/G]TGCTAACCAGTCACG | 56916 |
rs529172800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254790 | TGAGCTTTTTCAAAT[C/T]AATAGTGTAAATTAG | 56916 |
rs529285661 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215249 | ATACTTAGTTAAAGG[A/G]TTAGTGCTGAATTGT | 56916 |
rs529379475 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256576 | CCATGTTGGCCAGGC[C/T]GGGCTGGAACTGCTG | 56916 |
rs529386966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257233 | TCATTTTTTGAGAAT[A/G]ATTTGTTTTACCTAA | 56916 |
rs529423754 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278018 | TTGCATCAGTCTGCA[C/G]TAGCTTCCTTTTGGG | 56916 |
rs529480627 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262713 | CCATAAGGAATTACT[A/G]GGTCTTAGATTTTAT | 56916 |
rs529493622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235834 | CAGAGTTTTTTTCTT[A/G]TAAAAATCTTTCTAA | 56916 |
rs529518506 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267499 | ATCACATGTACCCCT[C/G]TTGTTTCTATTTTAC | 56916 |
rs529523114 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227574 | GGTTGGGAGATAAAG[A/G]AGTCAAGGATCACCC | 56916 |
rs529556855 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276511 | TTTCCAAATTACTGT[A/G]AAATTTAGATTACGT | 56916 |
rs529569664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229269 | ATTAATTTATGATAA[C/T]GATGGTGGGAAAATG | 56916 |
rs529576757 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265490 | CTACTTTCAATAAAA[C/T]ACTTGTCAGAATTCA | 56916 |
rs529664089 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230547 | CCAGATAATTCTTTG[C/T]TGTGAGGTGCTGCCC | 56916 |
rs529687920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237360 | CGTAGCTGGTAATCA[A/G]CATTCCTTTAGTAAA | 56916 |
rs529737202 | snp | G/T | 1.64817e-05 | 0.00287064 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274705 | ACATACCCTATTGTA[G/T]CAGATGCAAATAATG | 56916 |
rs529772234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224468 | AGCTGATCTGTATTT[C/T]ACATACACCAAGTTT | 56916 |
rs529800674 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273909 | TATTGGCAGTCTTTT[A/T]AAAAGAACTCAAATG | 56916 |
rs529868416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210603 | AGAGGTTTCAAAGTA[A/G]TGAAGGGCAGGGTTT | 56916 |
rs529907016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244312 | GTTTCCTACAAACAA[C/T]GCTACAGTTTCCTAA | 56916 |
rs529927288 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279540 | CAAACTATGGCCTTA[A/C]GGCAGTGACTATTTT | 56916 |
rs529959998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243844 | TTTGAAAAAAGCACT[C/T]ATTCAACATCTCAAA | 56916 |
rs529979810 | snp | C/G/T | | | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209191 | GATTTCCACTCGAAT[C/G/T]TATGTTCATTGAACA | 56916 |
rs530040030 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212710 | CAGGCTAGTCTCAAA[C/T]TCCTGACTTCAGGCT | 56916 |
rs530075342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252071 | TGGTCAGGCTGGTCT[C/T]GAACTCCTGACCTTG | 56916 |
rs530104035 | in-del | -/AA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254961 | CTTAATAAAATTATC[-/AA]AAGTCAATATTATGC | 56916 |
rs530106110 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206213 | TGTTGCAGCACTATT[C/T]ACAACAGCCAAGATT | 56916 |
rs530112904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281381 | ATTTATCAACATGAT[A/G]TAAGTAACACTTCTA | 56916 |
rs530178768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238900 | AGGTAGCACAGGCTG[C/T]GGCTTAGGTACTGAG | 56916 |
rs530188737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218870 | AGGCTGGAGTGTGGT[A/G]GTGGGATCATGGCTC | 56916 |
rs530196486 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276039 | TCTGACCTCGTGATC[C/T]GCCCGCCTCGGCCTC | 56916 |
rs530204788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258218 | GGAGTGCAGTGATGC[A/G]ATCTCAGCTCACTGC | 56916 |
rs530337111 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258965 | TCTAAAATCAAACTA[G/T]TCTTCTTTTTTTGTT | 56916 |
rs530356153 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218089 | TCATATTTGTCTCTT[C/G]ACTCTTTGCCTTATA | 56916 |
rs530365397 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282871 | AAAAGGACAAAATAG[C/T]CATTTAGGAATTAAT | 56916 |
rs530375731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213982 | ATTTGAAGGATGACT[A/G]GAATAGTCATAGAAA | 56916 |
rs530407323 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214631 | GGAGGGAGGTATCTG[A/G]AGAGAGGCATCAAGT | 56916 |
rs530419489 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94251068 | CTTTTTCTATTTGTT[A/C]AGTCTTTCTTAATAG | 56916 |
rs530461030 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220243 | CGGCTTTTACTGATT[G/T]TATTTATTATTATTA | 56916 |
rs530533711 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214352 | ACTGCAATCTCTGCT[C/G]TCGGGTTCATGCCAT | 56916 |
rs530538149 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207465 | TAACTCTCTAGATAA[C/T]TTAACAGGACAAAGG | 56916 |
rs530588477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282120 | TTTTTTTTTTTTTGA[A/G]ACGGAGTCTCGCTCT | 56916 |
rs530653753 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265875 | TAGGTTAAGATTAGC[A/T]GTAGGATCTCATTAA | 56916 |
rs530697341 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226022 | TTTAGATTGGAAACA[A/G]TGAATGAAATTTGAG | 56916 |
rs530697509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275694 | TTCTTTTTTGTGCTT[A/G]TTAAAATATAACACT | 56916 |
rs530706788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269430 | GCTTTGGAGTGAGAT[C/T]GACATCCTGAATTAA | 56916 |
rs530718773 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276067 | CTCCAAAAGTGCTGG[C/G]ATTACAGGTGTGAGC | 56916 |
rs530725251 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212930 | GAGGGCATACACTTA[A/G]CCTCTGCCCCCTGAT | 56916 |
rs530736412 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287560 | TCTCCTAAGAAATTG[A/G]CAATTTGAAATGCAA | 56916 |
rs530780207 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277214 | GTGTTTTATCTGGGC[C/T]ATTCTTCTGTTAGGT | 56916 |
rs530815527 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227356 | TTGAACAGAGAGGTA[A/G]AATTATCTGAGTTAG | 56916 |
rs530819657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258219 | GAGTGCAGTGATGCG[A/G]TCTCAGCTCACTGCA | 56916 |
rs530837684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268773 | GATAATTAATATTTC[C/T]TATTTTTAATATGGA | 56916 |
rs530863338 | in-del | -/TAA | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265974 | TTGCTGATCATTGGT[-/TAA]TAATTTAAAATCAAG | 56916 |
rs530881570 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261387 | TACAGTAACATCTTT[A/G]GATTTCTACCGAATT | 56916 |
rs530901187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262211 | CACTGGCTCTTTCTC[A/G]AAAATTTGGTAGCTG | 56916 |
rs530940617 | snp | A/G | | | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209513 | GCAAAACTCTGTTTC[A/G]TAAACAGCTTTTAAC | 56916 |
rs530943862 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236009 | TCAGTTCTAGAAATT[G/T]AAAGGTAATGTTTAT | 56916 |
rs531027540 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271788 | TTTCAGGAGCTATCT[G/T]ATCCTTTCCAGTTGA | 56916 |
rs531051065 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246774 | AAACCATCTAAGTCC[A/G]TGAGTACTGTATTAT | 56916 |
rs531081006 | snp | C/G | 3.2981e-05 | 0.00406071 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289586 | TCAACTTGGTGCACT[C/G]AAGGACATTTACATT | 56916 |
rs531096064 | snp | A/G | 0.000183503 | 0.00957694 | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208141 | GGGGAGGCGGACGAA[A/G]GGGAGTGAAAAGCAA | 56916 |
rs531098387 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233268 | TCTAGTTCTGATCTC[G/T]AGAGTGCCTACCATG | 56916 |
rs531210145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283554 | TTGACGGCCGGGCGC[C/T]GTGGCTCACGCCTGT | 56916 |
rs531215268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276680 | ACGTATTCTTTGATT[C/T]TGTTTTTTAACAACC | 56916 |
rs531230681 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291488 | AAATACTGTAACCCA[G/T]TATCACTACAGAGCA | 56916 |
rs531279827 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287558 | CATCTCCTAAGAAAT[G/T]GGCAATTTGAAATGC | 56916 |
rs531284636 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224845 | TCCCTCATGATTATT[G/T]TGAGGTTTAAATGTT | 56916 |
rs531306665 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235064 | GGTTGGTCACCACTT[G/T]AACAGCTATATTCCT | 56916 |
rs531332730 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230692 | GCAGCAAAACTACCC[C/T]CTACCCCAACTTTGA | 56916 |
rs531540448 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249274 | TAGGTGGATATATAA[C/T]AGTGAACATAGATGA | 56916 |
rs531540670 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282222 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 56916 |
rs531551794 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210705 | AGCACTTTGGGATGC[A/T]AAGGTGGGCAAATCA | 56916 |
rs531603649 | snp | C/T | | | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94251874 | TTATTTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 56916 |
rs531660364 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243869 | CTCAAACCTACCTAA[C/G]CATTCTGGTTCAAAA | 56916 |
rs531754790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279377 | ACTCCTGAGCTCAAG[C/T]GATTCGCCCGCCTTG | 56916 |
rs531773407 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223152 | TTCTTCATTTTTTAT[C/G]TGCAGTCCAGTGCTC | 56916 |
rs531775420 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272544 | GCTACCACTATTCTT[A/T]TACCTATCCTCGTGG | 56916 |
rs531808816 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222910 | CGGAGGTTGCAGGGA[G/T]CTGAGATTGTGCCAC | 56916 |
rs531855804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258049 | TTTTCTCATTTTTTT[C/T]CCTAGTTGTTATTTG | 56916 |
rs531944586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225046 | AATATGTAAGGGTAA[A/G]TGGTGGTTTTATTGG | 56916 |
rs532007924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223805 | CTGGGCTGATGTCGA[A/G]CTCCTGACCTTGTGA | 56916 |
rs532028435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231753 | AAACCAAGATCTAAA[C/T]TACATTTGGCTATTA | 56916 |
rs532096967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268564 | ACTCAGTGTGTTGAC[C/T]GTAGGATGGGTGGGT | 56916 |
rs532108374 | snp | A/T | 0.000214498 | 0.0103539 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274835 | TTAACTTTGGAAATT[A/T]AAAATAAAGTACAGC | 56916 |
rs532122861 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208700 | ATGCATTGTCCTGCG[C/G/T]TGTGCCCTTTTAAAT | 56916 |
rs532186324 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244940 | AAAGTGAACATTTTA[G/T]ATATTAATTGCTGTT | 56916 |
rs532235603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267643 | TCCCCTAACAAAACA[A/G]TAACTTCAAAATAGC | 56916 |
rs532271154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237969 | AGGTTATGCCAGTTT[A/G]TGCTTTTATCAACAG | 56916 |
rs532285260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286146 | GAAATTTTTCAACCT[C/T]CTGTGAAGTGAAGAG | 56916 |
rs532338065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228337 | TGCATTATCACTCTT[C/T]GTAAACAGCAATTAC | 56916 |
rs532377419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244352 | TGTCAGACATAACTA[C/T]TAGTGTAGATATGAA | 56916 |
rs532380139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239648 | TGCGGTCTCAGCTCA[C/T]TACGACCTCTGCCTC | 56916 |
rs532409525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246155 | GATGGAGTCTCGCAC[C/T]GTTGTCTGGGCTGGA | 56916 |
rs532445557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282791 | TGCCAGTAGGAGCCG[A/G]TATACTTCTGAGAAG | 56916 |
rs532447436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276178 | TATTAAATACAAGTA[C/T]GTCAGTATTTATTTG | 56916 |
rs532472813 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282442 | TATTTTTTATGGTTT[G/T]CACCTTTAAATTTTT | 56916 |
rs532486595 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280021 | AGGCACCTACCACTA[C/T]GCCCAGCTAATTTTT | 56916 |
rs532508441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232519 | AGAAGTCTAGGTATA[A/G]TAATGCAAAGGAAAT | 56916 |
rs532559967 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271844 | AATGTAGATAGTCTT[C/T]ATATCATAAGATTGC | 56916 |
rs532599715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94251334 | AGGAAGAGTTGAGTC[A/G]TACATGTTTAGTAAC | 56916 |
rs532627006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259847 | ATAACATTCTTATAT[C/T]TAATAAAAATCATCA | 56916 |
rs532631304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219512 | TGGTAGACTTAGATA[C/T]GAGAACGGGTAAAGG | 56916 |
rs532671623 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284412 | TGTAGTTGTAATGTT[G/T]TGTTTTGTTTTTGAG | 56916 |
rs532688639 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252160 | AGCCTATTTGAATAA[-/T]TTTTTTAAGTAACGA | 56916 |
rs532697245 | snp | C/G | 5.091e-05 | 0.00504504 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249617 | CATTGTTATTGATAT[C/G]TCTTAAATTGTTTTC | 56916 |
rs532776777 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212557 | AGTGGCACAATCTCG[G/T]CTCACTGCAACCTCT | 56916 |
rs532785772 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207901 | CCCGCCAGCACGGCC[G/T]CCGCCGCTCCCCTTC | 56916 |
rs532818185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222986 | ATAAATAAAATAAAA[A/G]TTGTTATGTCTTCAC | 56916 |
rs532927457 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276588 | TTAATATATGTAGTA[G/T]TCTGTGTTAGCAAGT | 56916 |
rs532973843 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262005 | CCTACATTTCTTCTT[C/G/T]CTCTGTCTTTTTAAA | 56916 |
rs532986510 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94253692 | TACACTTTGCATGAT[C/G]ATTTTCTGGAATTTG | 56916 |
rs533055193 | snp | C/G | 0.000475923 | 0.0154187 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208304 | ATTGTATCGTATATT[C/G]TTTTCATGGCCTTTT | 56916 |
rs533077404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254741 | AAAAGTAAACTTTCT[A/G]CTTGAGTTCAGTGAA | 56916 |
rs533120837 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220281 | GAGATGGAATTTTGC[G/T]TTGTTGCCCAGGCTG | 56916 |
rs533224587 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273427 | AGTAAAGTAAGTTAT[A/G]GCATCATTTGGAGAT | 56916 |
rs533260142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260745 | TATACAAAATTCAGA[A/G]TAAATGTTTATTCTT | 56916 |
rs533276035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94263600 | GTATTTTATTTAGTT[A/G]TCTTAGTATATCCAA | 56916 |
rs533289458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220904 | AAAATGTGAAGTACG[C/T]ATCACTGCATACCGT | 56916 |
rs533326607 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283633 | GATCGAGACCATCCT[G/T]GTTAACAGGGTGAAA | 56916 |
rs533338296 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226926 | CCAGGCTGCTCTCAG[A/C]CTCCTGGCCTCAAGC | 56916 |
rs533402167 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241671 | GAATCGTGAAGGTGT[A/C]ATCATCCTGCCACCA | 56916 |
rs533440518 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262512 | CATAGAGTTCTTTCT[-/A]AAACAGGAACTCTCT | 56916 |
rs533456086 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264558 | AACTCAAATATAAAC[A/C]TGAAGAATCAGGTTC | 56916 |
rs533468386 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272312 | AGGTGGACACAATTC[A/G]GTCCACAACAGTTGA | 56916 |
rs533506543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272198 | CAGGCCCCACACTTA[C/T]GAACTCATTTAGCCT | 56916 |
rs533548752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241995 | ATTCACACAAACACC[A/G]TTATCCTTCTATTCT | 56916 |
rs533553558 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264050 | GAACCATTTATAGTA[G/T]TATATTGAAATTGGT | 56916 |
rs533560751 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239423 | AGGGATGTTTTTATG[C/G]TGTTTGTTTTGAAAG | 56916 |
rs533560815 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268375 | AATTTTTGTTTATTA[A/G]GAATATTTCGTGGCT | 56916 |
rs533661580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234703 | AATTTCTGAAGATTA[A/G]TAAACAGTCTGTTCC | 56916 |
rs533688487 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272559 | ATACCTATCCTCGTG[A/G]ATTTTTTTCTGGTTA | 56916 |
rs533697087 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217990 | ACAGTGGGTTTCAGT[C/G]AAAAATGTTTGAAAA | 56916 |
rs533699614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264194 | AGTTTTGAAAACTTG[A/G]GGGGCTATACTTTGA | 56916 |
rs533708814 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262032 | TAAATGCTTCTAAAT[A/G]TTGGTGTTCTTCAAG | 56916 |
rs533717793 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277271 | TGCTCTATGAAGTAA[A/C]TTTAAGTAGGTGATA | 56916 |
rs533748778 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245940 | TAAAACTCTCTAAAA[C/T]GATTTTCCCACTGGG | 56916 |
rs533771413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241838 | GCACAGACTCAAGCC[C/T]AGTTGCCATGGCCAT | 56916 |
rs533856517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216294 | GGGAGTGGGGCACAA[A/G]CAGACCATAGCACCC | 56916 |
rs533867254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277612 | AGTCACAACTAAAAG[C/T]GACAGTAAAGAAATC | 56916 |
rs533870818 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223187 | TCTGAGCTGTAACCC[C/T]TCCTGTCTTCATTTT | 56916 |
rs533873419 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234419 | CCCCATTTCCATTAG[A/T]AATACTCAGAAATGT | 56916 |
rs533908332 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221202 | TTTCTGAGAAGATCA[A/G]TGGTGATATTAACAA | 56916 |
rs533980743 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291512 | CAGAGCAAATGAAGC[A/G]AGAGTTGGAGTAATA | 56916 |
rs533995212 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237497 | TTTAACTTACACATA[C/T]TAAAAAAAAAAAAAG | 56916 |
rs534129698 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284232 | CTCGGGAAGCTGAGG[C/G]AGGAGAATGACGTGA | 56916 |
rs534218431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243920 | AGGGAATGTTTTGAG[C/T]ATTAAGGAGAAGCTT | 56916 |
rs534231769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257467 | TTTCTTAAATCTTTT[C/T]TGGGGGAAAGTTAAG | 56916 |
rs534245739 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210804 | CCAGGCATGGTGGAG[C/T]GTGCCTGTAATCCCT | 56916 |
rs534293252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230643 | CTAGTCAAGACAATC[A/G]GAAATATCTCCAGAC | 56916 |
rs534324329 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266586 | CAAGGTAAGAGTTGC[A/G]TAAGCAATTTTTACT | 56916 |
rs534336321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279681 | AAAGCCTAAAATATG[A/G]TCTGGCCCTTTACAG | 56916 |
rs534338028 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239085 | AATTAGGATTTTCTG[G/T]TTTTTTAATTAAACT | 56916 |
rs534358606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219059 | TCAAGTGATCTGCCC[A/G]CGTTGGCCTCCCAAA | 56916 |
rs534408751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245345 | TGACAGTGTAATACA[A/G]ATGATCAGATGTTTT | 56916 |
rs534426425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94251561 | AAATGAGTCAGAAGA[A/G]CCATGTTATGAATGT | 56916 |
rs534490510 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249877 | TTCTAATTAAATGTT[A/C]TCCTTTTATCAATGT | 56916 |
rs534523191 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231260 | CTTGAGCACATTGCC[A/G]ATTGGGGAGGAAGAG | 56916 |
rs534529712 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288724 | TATAAAATTATTCAT[A/T]GTTACAGATCTATCA | 56916 |
rs534585448 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218418 | CTGACTCAGCCTCCT[C/G]AGTAGCTGGTACCAC | 56916 |
rs534585474 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255224 | AACAAATAGTCTGCT[C/G]TTTCTTGAAATCATT | 56916 |
rs534612974 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237581 | CCACACTTCATTAAC[C/T]ACCCTTAAATTATAA | 56916 |
rs534656953 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268918 | AAATTAAAATGTCTA[C/T]GATAACATGTTCCAT | 56916 |
rs534681099 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213936 | ACAATAAAAAACATC[A/G]TTTGACAATGGGCAG | 56916 |
rs534686023 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210176 | TCTCTTTATTGGGAC[A/T]TTTTTCCATACATAA | 56916 |
rs534711902 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226132 | AGAAGATTCTAGTGT[C/T]CCAGAAACTCCAGAT | 56916 |
rs534717756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275926 | CCTCAGCCTCCTGAA[C/T]AGCTGGGACTACAGG | 56916 |
rs534733478 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215581 | AGCTGTGATCACTAC[A/T]CTACATTCCAGCCTG | 56916 |
rs534831912 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273512 | TTGCATTCTGGGAAA[A/T]CAAAAGTGAATACAG | 56916 |
rs534897658 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267680 | CCTCATTTTCTTTCA[G/T]TATCTCAGAAAATCT | 56916 |
rs534905516 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258405 | AGTGATCCGCTCACC[G/T]CCACCTCCCAGAGTG | 56916 |
rs534920576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245802 | TGACATTGTATCTCT[A/G]ACAGTTTTTCTCCTA | 56916 |
rs534949467 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232242 | ATAAATCCAAGCCAT[A/G]GTGATATTCATTGTC | 56916 |
rs534956336 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94263005 | AGGTACTAGTTATAC[A/G]GTGAAAAGGGCATGG | 56916 |
rs534960772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267120 | TACAATATATTTAAT[C/T]AAGTGTGTCTTGCCT | 56916 |
rs534976590 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276216 | CCCGTGTCTAGTGCT[G/T]TGCTTTAAGTACTGG | 56916 |
rs534999000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232545 | GAAATGCATGTGATT[A/G]TCCTCAAATATTTGA | 56916 |
rs535012277 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234382 | TTTTTTTGTGTTTGA[A/G]TGTTTCTAAAATGCA | 56916 |
rs535062783 | snp | A/G | 0.00198702 | 0.0314573 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283094 | CAACTTTTTAGTGAG[A/G]TTTAACCTAATTTGT | 56916 |
rs535099928 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220392 | AGCTGGGACTACAGG[C/T]GTGTGCCACCACACC | 56916 |
rs535101928 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213609 | GAAGCCTCAATGTAG[G/T]GAAATGACTGTAGAG | 56916 |
rs535162837 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210084 | TATCAGTATTGGTCA[C/T]GTGAAATCTTTAATT | 56916 |
rs535167369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260339 | GCAAAATTAATACTT[C/T]TTATTTTATTTTTTT | 56916 |
rs535189978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227737 | TGAGAACACTCCTAG[A/G]CGTCTAAATGGAGAT | 56916 |
rs535247903 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207593 | GAAGAAAAAGCCTAG[G/T]CTGCGTGTTGCGTCA | 56916 |
rs535268881 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94253254 | GGAATACTGTCACTC[A/C]TTCCTTTGCATAGAA | 56916 |
rs535345280 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266816 | TGAATTGTAGGAGAA[A/G]AAAGTTTGCCTTTTA | 56916 |
rs535401206 | in-del | -/AT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270181 | ATAATTTTGCTAAAC[-/AT]GTGCTGTGTACATTT | 56916 |
rs535410201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209293 | TCATTTAATTTGCAC[A/G]ATAATCCTACAAGGT | 56916 |
rs535455006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247791 | AATATGTAACCTTTT[A/G]TGTCTAGCCTCTTAT | 56916 |
rs535477082 | snp | A/T | 1.68855e-05 | 0.00290559 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94240934 | GAAAAGAAAATTATC[A/T]TCTTCTTCAGAGCCA | 56916 |
rs535494336 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208726 | TAAATACAGCTTTGG[C/G]ACTGCCATAAGCACC | 56916 |
rs535521251 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270606 | AGTAGGTGTACATAG[C/T]ATCTAACAGTTAAAA | 56916 |
rs535535525 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234237 | ACGTTTGAAGATATT[A/T]ACTATTAAATCTAAA | 56916 |
rs535552918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242364 | TTTCAGAATAACTTA[C/T]ATTCTGAGATGTTCA | 56916 |
rs535572332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233552 | GGTAGGCCTGAAAAT[C/T]ACTTTATCTTTGTAT | 56916 |
rs535580042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283682 | TACAAAAAATTAGCC[A/G]GGCATGGTGGCGGGT | 56916 |
rs535671437 | in-del | -/A | 0.498903 | 0.0233891 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262937 | GTAGTTGGTTACAGA[-/A]AAAAAAAAAGTGTAT | 56916 |
rs535710589 | in-del | -/TTTTATTTTATTTTATTTT/TTTTTTT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275796 | AACATTAACATTTTC[-/TTTTATTTTATTTTATTTT/TTTTTTT]TTTTTTTTTTTTTTT | 56916 |
rs535719349 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210328 | CTTTGCTTTAATAAA[A/C]GATTGTTTTAAATGA | 56916 |
rs535745788 | snp | C/T | | | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94236992 | ATGGAGCAATTGCTG[C/T]TGCCTTGCTGATGTT | 56916 |
rs535746940 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239967 | ACTTAAAATATTACA[A/T]TTAGAATATTGTGGT | 56916 |
rs535754601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94253804 | AGATAAATATAAGAA[C/T]TCTTAAATTTTGCTT | 56916 |
rs535756667 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207967 | GGGCCCTGGCAGGTC[C/G]TTTCTCGAGGCAGGG | 56916 |
rs535813400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265068 | TATGAACTGTTTTTC[A/G]TTGATTTCCCCCACC | 56916 |
rs535814660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255784 | AGGATATTTATGCTT[C/T]AGCTTTATAATCATT | 56916 |
rs535833766 | in-del | -/A | 0.300169 | 0.244914 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284165 | CTCTACTAAAAATAC[-/A]AAAAAAAAAAAATTA | 56916 |
rs535932723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257598 | ATCCCCAAATTGTTT[A/G]TTTACTTTTTGTTAA | 56916 |
rs535945840 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256615 | TGATCCACCTGTTGC[A/G]GCCTCTCCAAGTGCC | 56916 |
rs535986904 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291677 | AGTTCCTAACAGTTG[A/G]CATTATCGTGTAGTG | 56916 |
rs535989853 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289654 | TATAATTTCCATATT[A/G]CATTTCTCATAGTAT | 56916 |
rs536007458 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232494 | TTCAAAGTTGAGTAC[A/G]TCAGGAATGAGAAGT | 56916 |
rs536050345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228323 | CATTTTCCCACAATT[A/G]CATTATCACTCTTCG | 56916 |
rs536066677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277403 | TTTCTGAAGGATGAC[A/G]ATTTTAAATTGATGA | 56916 |
rs536201485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262415 | CTTATCAGTTTCTCC[A/G]TGTCCAACACAGACC | 56916 |
rs536217682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216920 | CTCTTTGAAACCCTG[C/T]TTTCAGTTCTTTTGG | 56916 |
rs536247031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223393 | AGCTACTCAGGAGGC[C/T]GAGGCAGAAGAATCA | 56916 |
rs536262906 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286398 | CATCTTACCTGTTCA[A/C/G]GCTGATTATAACTTC | 56916 |
rs536322354 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284358 | AAAAAAAAAAAGAAA[A/G]AAGTAATTTCCATCT | 56916 |
rs536329656 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217715 | ATAATCTAAGTACAG[A/T]TTTAATTATATGTCG | 56916 |
rs536333661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210363 | GTGAATTTTGGAGAA[C/T]CTTGAAAACTGAGAA | 56916 |
rs536387717 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259304 | ATGAGAGATTAATAA[C/T]TTTATTTAAACCTGT | 56916 |
rs536408161 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284652 | CTGATCGGCTGATCT[C/T]GAACTGCTGGCCTCA | 56916 |
rs536429020 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212765 | GTGCTGGGATTACAG[A/G]CATGAGCCACCACAC | 56916 |
rs536468050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284278 | CTTGCAGTGAGCCGC[A/G]ATCGCACCACTGCAC | 56916 |
rs536554201 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250307 | TACATTTACACTTGC[A/C]CTGATTTATTTGAGT | 56916 |
rs536575264 | in-del | -/T | 0.00123431 | 0.024812 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218624 | AAATTTGAAATGGGG[-/T]TTTTTTCCCTCATTT | 56916 |
rs536584468 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249889 | GTTCTCCTTTTATCA[A/G]TGTTATAAAGTATTT | 56916 |
rs536603891 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280297 | TTACCATTTGATAAT[A/T]ACACCACCCTTGTTT | 56916 |
rs536604591 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206782 | GGCGCCCGCCACTAC[A/G]CCCGGCTAATTTTTT | 56916 |
rs536689982 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94205937 | CGAGTAGGTAGGACT[A/C]CAGGCGCCCGCCACC | 56916 |
rs536700110 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239367 | CTTTTAACCACAAAT[G/T]GCAGTCTTAACAGAC | 56916 |
rs536732910 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231849 | TTTTCTCAGAAAAAA[C/T]AGATTTTTCTTTTTC | 56916 |
rs536739422 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224829 | TCATGGGGGATATGT[G/T]TCCCTCATGATTATT | 56916 |
rs536769196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231294 | ATGAAGAGAGAAAAG[A/G]TTCAGGAGAAACATA | 56916 |
rs536782899 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242293 | CAAGTGATCCACCCA[C/T]CTCGGCTTCCCAAAG | 56916 |
rs536795677 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274263 | ACATAGGTTTCATAA[C/G]GAGTAATATTGTAAA | 56916 |
rs536810268 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219077 | TTGGCCTCCCAAAGT[G/T]CTGGGATTACAGGTG | 56916 |
rs536854860 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225222 | ACTTAAGAAATTTAT[G/T]TTTCACAATTGTGTA | 56916 |
rs536855066 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254566 | TAATTAATCAGCAGA[A/G]TTTAAATTAGTCTTG | 56916 |
rs536876721 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249909 | ATAAAGTATTTTCAT[A/C]CTGTTTATTTATGTT | 56916 |
rs536885957 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210888 | GCAGTGAGCCTAGAT[C/G]ACACCACTGCACTCC | 56916 |
rs536897724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237212 | TTTTACTGCTTTTCT[A/G]CCAATCAAATCTTGT | 56916 |
rs536966365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244050 | AAAATAAAAGTGTAT[A/G]TATGGCTGGACCAGG | 56916 |
rs536984582 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276885 | TTTAAATTACTATAT[C/T]ATTTATCACAGAATG | 56916 |
rs537016121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261037 | CAGTGGCAGAAAATA[C/T]GATAATGACAGATTA | 56916 |
rs537078083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245448 | GTGGCATCCGGATGA[A/G]TTTGGAACCGTACAG | 56916 |
rs537110508 | in-del | -/ACACACT | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257030 | TGTACAGTAAGAGTG[-/ACACACT]GTGGCAAGAGAGTGA | 56916 |
rs537114088 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262138 | ATGGTCACCTGTGTG[A/G]CATCTTTTTCTCCAG | 56916 |
rs537153533 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94253299 | ACTGCAGAAGAAGAA[A/G]TTAGAGCTTACATTT | 56916 |
rs537169479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288128 | AAGTCAATTGTAAAC[A/G]TGGCAATTTATTTTC | 56916 |
rs537211821 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239478 | GAAACAAAAAAATGT[A/G]TATCCAAAGTTTTTA | 56916 |
rs537307258 | in-del | -/AGGACAGTCATATTGGGTTC | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272164 | ATATTTCTTCTTACA[-/AGGACAGTCATATTGGGTTC]AGGCCCCACACTTAT | 56916 |
rs537320858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269690 | GTTGTTGTAATTGAG[A/G]CAGGGTCTGGCTCTG | 56916 |
rs537374310 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228904 | ATAATAGGCCAGGTT[C/T]TTTTAGAATTTTTCT | 56916 |
rs537391959 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235341 | CTAGTGGAAAAGATT[A/C]GTCGCTGTTGCAGGA | 56916 |
rs537401802 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277470 | CATTACATCATCTGT[A/T]TCAAAATTGGCTACG | 56916 |
rs537402685 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214270 | GCGTTCTTTTGTTTT[G/T]TTTTTTTTTTTTGAG | 56916 |
rs537417418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221059 | TTCTCAAAATGAACA[A/G]AGTAATACAAAGAAA | 56916 |
rs537421520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270389 | AAATCAAATCAACAC[A/G]ATTCAATTTTCTATT | 56916 |
rs537447071 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232187 | TTTTCTTCATGACAT[C/T]ATTTATTTTCTATCA | 56916 |
rs537460635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283766 | GGAGGCAGAGCTTGC[A/G]GTGAGCCGAGATCAC | 56916 |
rs537530743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221979 | AGTCACTAGGAGACA[C/T]ATGGGGGGTGTAAAA | 56916 |
rs537564310 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207629 | ACGCGCTCTTAAGGT[G/T]TCTCCGTGGTGTTTT | 56916 |
rs537594790 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282366 | CTCCCAAAGTGCTGG[G/T]ATTACAGGCGTGAGC | 56916 |
rs537626552 | snp | C/T | 3.30087e-05 | 0.00406242 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226246 | CGTTTCCCCAAATTG[C/T]TCCAATACAGTTCAA | 56916 |
rs537632304 | snp | C/T | 0.000325045 | 0.0127443 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290010 | ATGCAGCTGTATAGA[C/T]TATATAGCTTTCATT | 56916 |
rs537650722 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223455 | CTGAGATCACGCCAC[G/T]GTACTCTAGCCTGGG | 56916 |
rs537657617 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288986 | AAAGTGGCTAATTTA[A/G]TCATCAGCTGGTATG | 56916 |
rs537657671 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281795 | GGAGGCTGATGCGGG[C/T]GGATTGGTTGGGCTC | 56916 |
rs537671291 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247025 | TACTTGCAAGACTCA[G/T]CTACTTTTTGTATAG | 56916 |
rs537689781 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239767 | GAGTAGAGATGGGGT[G/T]TCACCATATTGCCAA | 56916 |
rs537775671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283325 | GTTTTTAGTTGGAAT[A/G]TATTTTTAATTCAGT | 56916 |
rs537852883 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291700 | GTGTAGTGGAGAGAC[A/G]GGGTATGAGGAGATT | 56916 |
rs537958468 | in-del | -/T | 0.0146672 | 0.084371 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252538 | AGGAATAGGTAAATG[-/T]TTTAAGTTTTTATTT | 56916 |
rs538033460 | in-del | -/TGTT | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259925 | TCATAAATGCCATAG[-/TGTT]TGTTCATTTGTTTTA | 56916 |
rs538079815 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208015 | AGCTTCTCTTTGTGG[G/T]CGGGCGCGAGGCCCG | 56916 |
rs538113966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225606 | CAGTTCAGCCCATAC[A/G]CCACATATTCATAAG | 56916 |
rs538135092 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233696 | CTAACAAAATAAATG[C/G]TAGGAAGTTCCTTTT | 56916 |
rs538167470 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209420 | TGAGCATAAACTAAT[G/T]AGTTAGTTTCTTAGG | 56916 |
rs538176119 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94290983 | CCAGTCTTGATGGTA[C/T]ATTGAACAGACTGAA | 56916 |
rs538209981 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258068 | AGTTGTTATTTGTCT[C/T]GGTTTTTCTCTTTAT | 56916 |
rs538212477 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257771 | TTTTGTCTCATTGTT[C/G]TGATCACCTCCATAT | 56916 |
rs538219188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218287 | TAATTAATTGTTTTA[C/T]TTTATTTTTTTTTTG | 56916 |
rs538221249 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266974 | TTTAAAATATAATAC[A/T]GTGAGGAAAAAGAAA | 56916 |
rs538271292 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284050 | AAGATAGCCGGGCAC[A/G]GTGGCTCACACCTGT | 56916 |
rs538272953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249184 | TTTTATGTTGTGACT[A/G]AACAATTAATATTTA | 56916 |
rs538290970 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236236 | AAGTAGCTTATTTAA[A/C]AGTAAGATCTTTTTA | 56916 |
rs538322272 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277669 | TCTTTATTGTTTAGG[A/G]AAAGTATAGTCTTCA | 56916 |
rs538341548 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283738 | GCTGAGGCAGGAGAA[C/T]GGCGTGAACCTGGGA | 56916 |
rs538351168 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249928 | TTTATTTATGTTGTT[G/T]ATTTACCTTGTTTAC | 56916 |
rs538351177 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258350 | AGCAGAGACGGAGTT[G/T]CATGATGTTGGCCGG | 56916 |
rs538378457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211800 | TTGCATATGACTCAG[A/G]TGCTTTGTTTCATTA | 56916 |
rs538396985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216237 | AAATGTCACCTCCTA[A/G]TACCATTACCATAAT | 56916 |
rs538398757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264022 | TGAAAGAAATTCTGT[A/G]AGTTTTCACAGAGAA | 56916 |
rs538405330 | snp | A/G | 0.000173145 | 0.00930283 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94253266 | CTCATTCCTTTGCAT[A/G]GAAACTTCGTTCATT | 56916 |
rs538415718 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272809 | TTTTCTTTTTTCTTT[A/C]TTTCCTTTTTCTTTT | 56916 |
rs538532894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248470 | TTAAAATACTGTTCT[C/T]GGAATTTCAGTGTGC | 56916 |
rs538532951 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256638 | CAAGTGCCGGGGTTA[C/G]AGGCGTGAGCCACTG | 56916 |
rs538607819 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275394 | ATACTAATAATACTA[C/T]TTGGTAATAATTGAT | 56916 |
rs538672704 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280958 | CTTTCCTCTGTTGAA[A/C]CTCAGACAAAAACAA | 56916 |
rs538775387 | in-del | -/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286268 | TTTCAGCAGCCTCTT[-/C]TCTTCTCTTCTATGA | 56916 |
rs538795476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275776 | ATGTAGAAGTTGTCC[A/G]ATTGTAACATTAACA | 56916 |
rs538902126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266009 | ATGGAAAAAAAAACA[A/G]GATGATTACTGGCCT | 56916 |
rs538918289 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238248 | TTGTGGGTGCTACCT[A/G]CAGTGTATCAAGATT | 56916 |
rs538962907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273402 | AGCAATGAAGATCTA[C/T]CCACTGCTCAGTAAA | 56916 |
rs538979644 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245284 | TGTATGGATGCAGAA[C/G]ATGTCGATGACAGTG | 56916 |
rs539000245 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287239 | GTCTCTTATTTACTC[A/G/T]TTTAGCTGTAATCAT | 56916 |
rs539012664 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278101 | CCACACTTAGACACA[-/T]TTTTTCAATGAGAGT | 56916 |
rs539117310 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230235 | TCCCTTCTCCATTCA[A/G]ACCTTAGAACTAACC | 56916 |
rs539154838 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232965 | AGTCTGGGTGACAGA[A/G]TGGAACCCCGTCTCA | 56916 |
rs539162347 | snp | C/G | 1.65094e-05 | 0.00287305 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226259 | TGCTCCAATACAGTT[C/G]AAGAGAAAACATTCA | 56916 |
rs539171772 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268259 | ATCTGTGTAGTTTTT[A/T]AAATTTCCTCATCAC | 56916 |
rs539177584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239853 | GCTGGGATTACAGGC[A/G]TGAGCTGTGCACCTG | 56916 |
rs539195177 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282425 | AACAGCTATTAGAAT[G/T]GTATTTTTTATGGTT | 56916 |
rs539214053 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213486 | AGTGTAAACCATTGG[G/T]TTGTGAGGGGCCTTT | 56916 |
rs539252489 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244631 | GCCTTTTAAAAGATA[C/T]TGTTAACGTCAGCCT | 56916 |
rs539267835 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270596 | ATTTTTTTTAAGTAG[G/T]TGTACATAGCATCTA | 56916 |
rs539336191 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231450 | AACTCTGTTGTTCTT[A/G]CAGGTTTTTTTCTTC | 56916 |
rs539336824 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237751 | CATTCCTCTGTGACT[A/G]CCCACAGGATTAGTT | 56916 |
rs539376602 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218918 | CTGGGTTCAAGCAAT[A/T]CTCATGCCTCAGCCT | 56916 |
rs539382685 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245900 | CTGACTGTGGTCAGT[A/G]GAAGAGGACATGATG | 56916 |
rs539411298 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208099 | GCATGAGGGTCAGCT[C/G]GTGGTTTCAGTAAGG | 56916 |
rs539421488 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254448 | TACTTGCCCGAATAT[C/T]TTATAGTAAAAGTAA | 56916 |
rs539428397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288165 | ACAGCATATTCCTCA[A/G]AGTTGGTACAATACC | 56916 |
rs539450660 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239404 | ATCCTGCGTATTAAA[C/T]ACTAGGGATGTTTTT | 56916 |
rs539475715 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240692 | AATGTGATGGTTTAT[A/G]AATATAGTATTACAG | 56916 |
rs539493588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221725 | TCACTTCCAACTCCC[A/G]TTTAGCTCTTATATG | 56916 |
rs539551761 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247126 | ATTGCTTATTGTTTT[C/G]ATTGAGAGGGACAAT | 56916 |
rs539615574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220673 | GCCTTTTTCACGATA[C/T]TGATATTTGCACTCA | 56916 |
rs539664045 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215173 | CAAAATGTGAGCCAT[C/T]GTTAAACCTGTAGAT | 56916 |
rs539728388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221090 | ACAACACAGTATGTA[C/T]TTCCAGTGATAAAAC | 56916 |
rs539737836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94253134 | CTGTGTAAAGTCAAA[C/T]ATTACTTTCATTGTA | 56916 |
rs539752072 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252320 | TGGGGCTGCTAGGAA[C/T]ATCTGAGACATCATA | 56916 |
rs539777610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215234 | GTTAATTGAAAAGCA[A/G]TACTTAGTTAAAGGG | 56916 |
rs539808166 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254762 | GTTCAGTGAAGACAG[A/C]AAAGTAGGTGAATGA | 56916 |
rs539866398 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276800 | ATACGAGGACACAAG[-/T]TTACCTACTTATAAA | 56916 |
rs539931642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254930 | CCCAAACCCTACCCT[A/G]GAGCAGATTTAATAT | 56916 |
rs539984789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269817 | GGGACTACAAGCATA[C/T]GTCACCATGCCTGGC | 56916 |
rs539995316 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94253860 | AGGAATTGTATATAG[A/G]CCTGTTGTAAAAGCA | 56916 |
rs540015430 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213706 | GAATGTGGAGGATTT[A/C]CAGATAACTCAAATG | 56916 |
rs540047232 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276591 | ATATATGTAGTATTC[G/T]GTGTTAGCAAGTTTT | 56916 |
rs540123646 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271208 | ATATATGTGCTTTTT[C/T]TACAGCTGCCTTTAA | 56916 |
rs540167975 | snp | G/T | 3.30017e-05 | 0.00406199 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270849 | TTCTAAGATTTGTTG[G/T]TGAAAGTGTCATTAA | 56916 |
rs540184709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270478 | TAATTTGGAGGTACT[A/G]TATTATGACCAAATA | 56916 |
rs540187428 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94263099 | GGTAGGCTAGTCTTG[C/G]TAGTTGTTACGAGGA | 56916 |
rs540237744 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222075 | AGTCACTGGTGATAA[A/G]GGCTATATATTTGCC | 56916 |
rs540275689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284899 | ACTCTTAAATATAGT[C/T]TACATATATCCAAAT | 56916 |
rs540282542 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267876 | TTAGAAAACTGTGAA[C/G]CGTCAAAATAGATGG | 56916 |
rs540301508 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208961 | CCTCAAAATATTGAT[C/G]ATCTACTGTGAGCTA | 56916 |
rs540315757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247883 | TGGGGTACATGTGCA[A/G]GTTTGTTACAAACGT | 56916 |
rs540320655 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223714 | CTGGAACTACTGGCG[G/T]GCACCACCACTCCCG | 56916 |
rs540347351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241503 | ATGACCCTGTCTCCA[A/G]TAAGGTCACATTCTG | 56916 |
rs540402176 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229994 | ATAGCTACACCCATA[C/T]TACTTGACCATTGAG | 56916 |
rs540427540 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216310 | CAGACCATAGCACCC[C/T]CTTTGTTGTTTGCCA | 56916 |
rs540431829 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283416 | TTTTTTCGGCAAAGC[A/G]TGGCTACTGATGTAT | 56916 |
rs540525604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228360 | GCAATTACAATAACT[A/G]CTGAACACTTTGCCT | 56916 |
rs540562361 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219957 | AGTAGCAGATGTCTT[G/T]TCTTTATAACTGTTT | 56916 |
rs540564262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227889 | GTAAGGGACACTAGT[A/G]TAGTATAGCTGAAGA | 56916 |
rs540574295 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265300 | ACCTCCTTTCCTAGC[C/G]CATTTTCTTTTTAAT | 56916 |
rs540627179 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272363 | GATCTGTATCTCCTA[A/T]GTAACTTTTTTAAAC | 56916 |
rs540637996 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239088 | TAGGATTTTCTGGTT[C/T]TTTAATTAAACTTCC | 56916 |
rs540639305 | snp | A/G | 6.62361e-05 | 0.00575445 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94278669 | GTTGTGTGCAATGTC[A/G]GAGAAGCAGGAGCAA | 56916 |
rs540639798 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229221 | CTAGCCAGCTTTCAC[G/T]CAGTAGTTGTAGTAT | 56916 |
rs540738113 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244688 | AATGTATGGATGGCT[A/G]CCCACATTTGCATTT | 56916 |
rs540787859 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288864 | TAGATTATCTGCCAC[C/T]GTGACACAAAGAGAT | 56916 |
rs540799157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286746 | TTGTATTTGTATAAA[C/T]TTGGTCAGTCTAAAA | 56916 |
rs540802051 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242097 | GGAGTACAGTGGTGT[C/G]ATCTTGGCTCACTGC | 56916 |
rs540922458 | snp | A/T | 0.0267878 | 0.112589 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269509 | TTTTTTTTTTTTTTT[A/T]ATCTGTTAAAGTGAT | 56916 |
rs540944045 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260236 | TGATGTGTTCTTTCA[A/T]CAGAAGACAGTAATA | 56916 |
rs540947917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211264 | GCAACAAGAGCAAAA[C/T]TCCATGTCAAAATAA | 56916 |
rs540980216 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217803 | TGTGTCATAAAATCA[A/C]TTTCTTGGGTCCTGA | 56916 |
rs541013265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286028 | AGCAAATATCCAAAT[A/G]TATGGATTTTATTCT | 56916 |
rs541015735 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257814 | TAGTTATAATGCACT[G/T]TTTGTCATTTGTAGG | 56916 |
rs541027632 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259720 | TGTTATAATGAACCC[A/C]CATGTGTTTCTTCCA | 56916 |
rs541048656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268332 | TAGACTCTTTTCCCA[A/G]TGTGTGTTGGTGATG | 56916 |
rs541144053 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273014 | TTTTGCCATGTTGCC[C/T]GGGCTTGTCTCAAAC | 56916 |
rs541151884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279904 | ACTTTTGCTCTTGTC[A/G]CCCAGGCTGGAGTGC | 56916 |
rs541156525 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284532 | GCCTCCCAACTGCTA[A/G]GATTACAGGTGTGTG | 56916 |
rs541156696 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266751 | TTCTCTAAACAGAAC[A/T]AGTTCTTCATGACGA | 56916 |
rs541172629 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286976 | TTCACACCATTCTCC[C/T]GCCTCAGCCTCCCAA | 56916 |
rs541180706 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257085 | TTTTTGAAAGAAAAA[A/C]GTCCTTTGAGTAGTC | 56916 |
rs541184424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266340 | TCACAAAGTCCTGTT[A/G]CTTGTAAATAGTTTG | 56916 |
rs541214387 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94251992 | GAGTAGCTGGGATTA[C/T]AGGCATGCACCACCA | 56916 |
rs541247753 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265459 | ATCATATAAGTCTAC[A/G]TATTTCCCCAATTTG | 56916 |
rs541280706 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231547 | CCTAGATTTAACAGT[C/T]GTTTTCCTTATTTGT | 56916 |
rs541284002 | in-del | -/TTA | 0.00198502 | 0.0314415 | utr-variant-3-prime, nc-transcript-variant, cds-indel, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291182 | TTTCTTTTTTTGTTG[-/TTA]TTGTTGTTGTTGTTA | 56916 |
rs541318242 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232897 | AGGTGGGAGGATTGC[G/T]AGAGCCTGTAAGACA | 56916 |
rs541436840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212422 | TCAAGTGATCCACGT[A/G]CCTTGGCCTCTGAAA | 56916 |
rs541442657 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219402 | TTTTGTTCGAATGAG[C/G]CTTAATCTCCTACTA | 56916 |
rs541512692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220736 | GTGCCTTAGCACCAC[A/G]GATCAAGGCCAAGGC | 56916 |
rs541524411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245609 | TTTCCATTCATTTTC[A/G]GATAACCTGTTTTTT | 56916 |
rs541552280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220202 | TTCTGATTATTGACT[A/G]TACCAGTATGTTGAT | 56916 |
rs541627474 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287795 | ACTTTAAAAATATAT[A/G]TATATTACCACAATC | 56916 |
rs541639632 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264512 | ATGAGTTTGATGTGT[A/G]ACAGTAGAATATAAA | 56916 |
rs541739948 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238242 | AGTATTTTGTGGGTG[C/T]TACCTACAGTGTATC | 56916 |
rs541801130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269287 | TATGTCCAGACCCTT[C/T]CCTGTGTGCAAACAG | 56916 |
rs541827246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282608 | ACGGAATTGTGTAGT[A/G]TGTTTAAATTGCATT | 56916 |
rs541843687 | in-del | -/T/TT | 0.00308227 | 0.0391578 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284948 | TGGACATATTTTGTA[-/T/TT]TTTTTTTTTAGAGAA | 56916 |
rs541848357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283512 | CCCACATTCCAAATA[C/G]TTCTGCAGTTCATGA | 56916 |
rs541902243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257823 | TGCACTTTTTGTCAT[C/T]TGTAGGTCTTATCTA | 56916 |
rs541932723 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241888 | GCAGGCATTCAAGTG[C/G]CTGTGGACTTAACTG | 56916 |
rs541937202 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227043 | AGAGCGTGGTCAGAA[A/G]AGCCTCAATTGAGAA | 56916 |
rs541946997 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223261 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 56916 |
rs541956919 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228142 | TTTTCACATGAAGCT[G/T]TGATAAACATGCCTA | 56916 |
rs541963657 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260589 | TGATCCACCTGCCTC[A/G]GCCCCAAAAGTGCTG | 56916 |
rs542019940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246042 | CGAAACCCAAGTGGC[A/G]GAGTACCTTGTATTG | 56916 |
rs542020624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214333 | AGTGGCGCAATCTCA[A/G]CTCACTGCAATCTCT | 56916 |
rs542024044 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94253562 | TGTTGGTTAAGCAAC[A/G]TGGCCATTTTATGGA | 56916 |
rs542156739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239425 | GGATGTTTTTATGCT[A/G]TTTGTTTTGAAAGTT | 56916 |
rs542179693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256177 | TTATGCTGACCAATG[C/T]GACATGCATCAGTAA | 56916 |
rs542214844 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94251205 | TAGATGTCTTAGCCT[A/G]TACTTGCACAGATAT | 56916 |
rs542240185 | snp | G/T | 0.000178939 | 0.00945714 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291172 | TGATAGGCTGTTTCT[G/T]TTTTTGTTGTTATTG | 56916 |
rs542278205 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228197 | AATGTAGTGAAGATC[C/G]TGCATGGTTAATCCT | 56916 |
rs542344655 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243351 | TGCACATGCAATTTA[C/T]TTGTGTCTCTTGAAC | 56916 |
rs542347910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249344 | AAGGCATCAGTATAC[C/T]TGAATTATATTGAGT | 56916 |
rs542370842 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283877 | AAAAGATGAGTAATT[A/T]AAAAAACTTGCTTGT | 56916 |
rs542490357 | snp | A/C | 0.00212435 | 0.0325218 | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208180 | TTTAAAAGATACCCC[A/C]GTCCACCTTCTAATT | 56916 |
rs542512568 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254488 | TTTTACCAGAGGTAT[A/G]TGTGCCAGATGTTTT | 56916 |
rs542584581 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217309 | TTACATTAAAATGTC[A/G]TCATTATAGTCTAAA | 56916 |
rs542630165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224226 | TTTTGGAAAAAAGTA[C/T]GATTTGCTTTTTGCT | 56916 |
rs542689314 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230474 | TTCATTCATTCCCCA[C/T]GTATGGGCATTTTGG | 56916 |
rs542707492 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248710 | ACTTAGTATTATGAA[A/T]CACATGCAATTTTCT | 56916 |
rs542734909 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242865 | AGGCTTCAGTGAGCC[A/G]TAATTATGCCACTGC | 56916 |
rs542802898 | snp | A/G | 1.72791e-05 | 0.00293926 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284933 | TATATTTAGTAACCA[A/G]TGGACATATTTTGTA | 56916 |
rs542869680 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264978 | AATTTATTTCTGTAT[C/T]GTGCCTAGAAAGTGA | 56916 |
rs542933458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215747 | GTCTGCTTTTTCATA[C/T]CTGTCTAAAATATTG | 56916 |
rs542934623 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222110 | TACGGAGAGGGTACC[C/T]CTCCCAGAGGAGCCT | 56916 |
rs543020073 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223723 | CTGGCGTGCACCACC[A/C]CTCCCGGCTAATTTT | 56916 |
rs543020280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272994 | GTATTTTTGTAGAGA[C/T]GGAGTTTTGCCATGT | 56916 |
rs543042101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237885 | TAGGCTAAATTTCAA[A/G]CTAGGATGTTCAAGC | 56916 |
rs543055976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230751 | CTGGCAGTAGATAAA[A/G]TCTCCTAGGAAGCAT | 56916 |
rs543128053 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238504 | AGTTAGAGGTGAATG[G/T]TAGCTGTGTCTTCCT | 56916 |
rs543148221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231637 | ATTTCTCCCCTTAAT[A/G]CTGGTTATGTATCTG | 56916 |
rs543162562 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243993 | TCCCAAGCAACAGAT[A/C]TAAAGGAATCCACAT | 56916 |
rs543181649 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266392 | TCCATTAGACTGAGG[A/T]TTTTTTAAATGAAAT | 56916 |
rs543260787 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211400 | CTCTGGAGAGGACAA[G/T]ATACTGAAGTTAGAT | 56916 |
rs543269752 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235840 | TTTTTTCTTGTAAAA[A/C]TCTTTCTAATTTTGT | 56916 |
rs543283588 | snp | G/T | 0.000372648 | 0.013645 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248436 | CCCTCCTCAGCTGGT[G/T]GTTGTCCATCTGTGA | 56916 |
rs543327452 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216935 | CTTTCAGTTCTTTTG[A/G]TTGTATACCCAGAAG | 56916 |
rs543337696 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286761 | TTTGGTCAGTCTAAA[A/C]TTTTGCCTGTTATGT | 56916 |
rs543341369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230087 | AAATACCATTAATTA[C/T]TTTGTATTCCTTTTA | 56916 |
rs543341609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244800 | TTCTTACAGTGTATC[A/G]AGCTCTCTCTCTACA | 56916 |
rs543353762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250605 | TACACAGAAAGCATT[C/T]GTAAAGCAGTGTAAA | 56916 |
rs543356838 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236398 | ATGCATATGTTCTTG[A/C]AAAGATTCAGACAAT | 56916 |
rs543367385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233790 | ATTTTTCACATAACT[A/G]CACTGAAATGGAAAA | 56916 |
rs543380897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252519 | GAATTCTTCTGTATT[C/T]AATAGGAATAGGTAA | 56916 |
rs543432377 | in-del | -/ATAAG | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264415 | GTGAATGTTTCTCTT[-/ATAAG]AGAATAGCTGCCAGG | 56916 |
rs543502039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224994 | GCACTGTGTTTACTT[C/T]AATACGACTCCCTTC | 56916 |
rs543532635 | snp | A/G | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94274773 | AATTTATGGTGCCCT[A/G]CTTTGAAGGTCCTCT | 56916 |
rs543605278 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258533 | TGGAAGTGGCCTTAG[C/G]ATTTCATTTTCCTGT | 56916 |
rs543669821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275539 | TCCTTTAAAAATTCA[C/T]GCGGAATTTTATTTT | 56916 |
rs543689119 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252096 | ACCTTGTGATCTGCC[C/T]GCGTCGGCCTCCCAA | 56916 |
rs543703381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244320 | CAAACAATGCTACAG[C/T]TTCCTAAGCCTTTGG | 56916 |
rs543726240 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254333 | AATCTTTAATGGTCT[C/T]TTATGTTGTTGCAGA | 56916 |
rs543760294 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230271 | GTTTAGTTCATTGTC[A/T]TACTTTCGTGTATTT | 56916 |
rs543787241 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256659 | TGAGCCACTGCATCT[A/G]GTCCTTTGCTTTGTT | 56916 |
rs543797100 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206946 | CATTTTTAAATGACT[A/G]AAATAACTGGATTGT | 56916 |
rs543876489 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220840 | AGTAAAAATTAGTAA[A/T]TTTATTAAATCTCAA | 56916 |
rs543878969 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269951 | GTGCTGGGATTACGG[G/T]CATGAGCCACTGTTT | 56916 |
rs543883716 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206245 | GGAAGCAACTTAAGT[C/G]TCCATTAACAGGTGA | 56916 |
rs543885820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213721 | ACAGATAACTCAAAT[A/G]TTCCTTGCTTGGACA | 56916 |
rs543891334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246648 | TCCTTCACCCTGATA[C/T]GTGGCATGTACGTAT | 56916 |
rs543948308 | in-del | -/TTA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248561 | TTTCACCAGTATGTC[-/TTA]TTATTCCCCTGCTCA | 56916 |
rs544000558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282733 | AAGAGAATCCACTTA[C/T]ACAATTTGATCATGA | 56916 |
rs544134608 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268957 | ACTTTTATAGTAGTA[G/T]CATAGAAATTATATT | 56916 |
rs544148419 | snp | A/T | 3.29891e-05 | 0.00406122 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270706 | ATAGATGTGTAATAT[A/T]TGGTAACTCTCTCTT | 56916 |
rs544168996 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221379 | GTTTTTTCGTATGGT[A/T]CCAGTTTCCACATTG | 56916 |
rs544207145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276579 | TTATGTAGTTTAATA[C/T]ATGTAGTATTCTGTG | 56916 |
rs544209900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276906 | TCACAGAATGTTAAA[C/T]TATTAATAATGGTTT | 56916 |
rs544219190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234619 | TAGTTGAAATGTAAA[A/G]TGATGTTTAGGTATC | 56916 |
rs544236592 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227818 | ACATGTCTGAATTTA[C/G]TAGGTGACAGAGTAT | 56916 |
rs544281792 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214616 | GAGGGAAGGACTGAG[G/T]GAGGGAGGTATCTGA | 56916 |
rs544287539 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243578 | ACATCAGTCAGTTCT[G/T]TTTTTAAAATGTGAA | 56916 |
rs544333929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228475 | AATTAACACTAGTAC[A/G]GTACTATTATCTAAT | 56916 |
rs544373970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222216 | CTCATATCAATGGTT[C/T]GGCATATTTTGAAAT | 56916 |
rs544423589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240060 | GTAATAGCCATGTTA[A/G]TGAAATTTTTAAGCT | 56916 |
rs544440336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232732 | CCAAGGCGGGCGGAT[C/T]GCTTGAGCCTAGGAG | 56916 |
rs544441048 | in-del | -/AA | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239066 | AAATTACAAGGAAAT[-/AA]AAAATTAGGATTTTC | 56916 |
rs544448851 | snp | A/G | 6.76384e-05 | 0.00581503 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208277 | ATTGCCTTGGGAATA[A/G]ACTGCTGTGGCATTG | 56916 |
rs544515981 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227104 | AGCAAAGACATAAAG[C/G]GGGTGAGAAAGTGAA | 56916 |
rs544552691 | snp | A/G | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233083 | ACAGAAATAACATGA[A/G]TACATATAGAGAAAT | 56916 |
rs544570958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272050 | CAAGATGAGTGTATC[A/G]GTAGCTTGCGTTTCT | 56916 |
rs544617942 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277809 | ACTGCCTTTTAAACA[G/T]TTACTAATTTGAATT | 56916 |
rs544618465 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248890 | GGAGGTTGAAGAAGA[A/T]GATTGTATTTTTCTC | 56916 |
rs544628554 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284018 | TTTGACATTGGTCAC[A/T]GCACTGTAAAGAGGT | 56916 |
rs544629384 | in-del | -/AT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279728 | CTAGTCTAGACTTCC[-/AT]ATAATGCACTTCTTT | 56916 |
rs544671122 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275359 | AATTTGAGTTAGGGC[-/A]GAAATAAAAATGAAA | 56916 |
rs544702236 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242558 | GTTGGGTTTATATTA[C/T]AGCAGTTGTTCACTT | 56916 |
rs544753993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227880 | GAAATCAGTGTAAGG[A/G]ACACTAGTATAGTAT | 56916 |
rs544782819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255202 | AATATATTAAGAACA[A/G]CCTGCTAACAAATAG | 56916 |
rs544882275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256996 | AGTTTCCTCCTTCCT[A/G]TGGAAATTCAAAAAT | 56916 |
rs544895177 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247854 | TTTTTCTTTTTTCAA[A/C]TTTATGTTAGAATTG | 56916 |
rs544949069 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256461 | TCCACCTCCCGGGTT[C/T]AAGCGATTCTCCTGC | 56916 |
rs544956549 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216995 | TTTTTAATTTTTTGC[A/G]GAACCTCCATACCGT | 56916 |
rs544965925 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271952 | GATGGCTTAGTCAGC[C/T]AGCATTGCCATAACA | 56916 |
rs545021341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265097 | CCCCCAAGTAGGGTA[C/T]TTTATTCTATCATAT | 56916 |
rs545023036 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274427 | GCCTCCCAGGTTCTC[A/G]TGCCTCAGCCTCCCG | 56916 |
rs545043311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218666 | GATGTATTAGAAACT[A/G]CTCTTTAATCTTATA | 56916 |
rs545080334 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236424 | ACAATTCAGAAATAG[A/T]GTAAAAATTAAGAGC | 56916 |
rs545092495 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243543 | ATTTATTGTCAAGTC[A/G]ATAGCTGTTTCACAA | 56916 |
rs545148202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264500 | TACTTTAACATAATG[A/G]GTTTGATGTGTGACA | 56916 |
rs545195244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222935 | TGCCACTGCACTCCA[A/G]CCTGGGCGACAGAGC | 56916 |
rs545207832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279391 | GCGATTCGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 56916 |
rs545211578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272292 | ATGTATTGTCAGTGG[A/G]AAGGAGGTGGACACA | 56916 |
rs545232435 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221940 | ACAAAGGGGATCTGG[C/T]AATGGGCAGCAAACT | 56916 |
rs545282570 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285791 | GTAAGAAGCAACTGA[C/G]ATCTTTAAGAGTAAG | 56916 |
rs545302902 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237295 | AGTTGCATTGTGGTT[C/T]TATTATAGGTTTACG | 56916 |
rs545331100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273802 | GGGTGTGTGTCGGAG[A/G]GGTGTTGTGGTTTCT | 56916 |
rs545347618 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287258 | AGCTGTAATCATTTG[C/T]CTTCAGCTGTGTCCC | 56916 |
rs545357074 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211528 | TTGTGGGATAATGCT[G/T]CGTTAGTTTATTTAC | 56916 |
rs545394800 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217994 | TGGGTTTCAGTCAAA[A/C]ATGTTTGAAAAACAC | 56916 |
rs545409197 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266705 | GAAAATATTAGACTA[A/T]CCTGATGAATAACCT | 56916 |
rs545421127 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222729 | ACATTTCAGGAGGCC[A/G]AGGCAGGTGGATCAC | 56916 |
rs545484508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219526 | ACGAGAACGGGTAAA[A/G]GGTACTGGATAAACT | 56916 |
rs545488452 | snp | C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226273 | TCAAGAGAAAACATT[C/G]AACAAAGATACAGTG | 56916 |
rs545555906 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206143 | TCAAGATAGGTGAAT[C/T]ATATGCAAAAGAAAG | 56916 |
rs545703491 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244003 | CAGATATAAAGGAAT[A/C]CACATTATGGACCAT | 56916 |
rs545718259 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240262 | ATGTATACAAGCATA[C/T]ATAAGTAGCATATGT | 56916 |
rs545764107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246701 | CCCACTACCTGTATC[A/G]AGTCCAGTCAACATG | 56916 |
rs545813706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281922 | TGGTGCACGCCTGTG[A/G]TCCCAACTAGGGAGG | 56916 |
rs545817753 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261544 | AGAACTGTCCATGAG[A/T]AATACTATAGAAATT | 56916 |
rs545821723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281286 | GCAGTTTATTCATAT[A/G]TAGGCTGCAATAAGA | 56916 |
rs545859944 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289301 | AACATAGAGGAAATA[A/G]CCCTAATCTAAGTAG | 56916 |
rs545877374 | in-del | -/C | 0.0040148 | 0.0446238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264701 | ATTTTTCTTTTTATG[-/C]TATAGTTCACAAAGA | 56916 |
rs545914734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232614 | TCGTTACTTTAGAGC[A/G]GTTTCTCAGAGCTGA | 56916 |
rs545931531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233155 | AGAATTAGCAGCATA[A/G]CAAAGTCTGAGTTCA | 56916 |
rs545940805 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238403 | CTAATAATGTATACT[A/G]CTTCTTATGGTGCCT | 56916 |
rs545956599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275999 | AGACAGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 56916 |
rs545962872 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287008 | TAGCTGGGACTATAG[G/T]TGCCCGCCTCCATGC | 56916 |
rs545990956 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244990 | AAGTGGTTACAGAAT[A/G]TTGGAAGAGGTTTAA | 56916 |
rs545991319 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94251920 | GCAGTGGCACAGTCT[A/C]GGCTAACTGCAACCT | 56916 |
rs545996183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220167 | AGATAAACAAATCTA[A/G]GTGTTCAGCACTATT | 56916 |
rs546037618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260484 | GAATAGCTGGGATTA[C/T]AGGCGTGCACCACCA | 56916 |
rs546052079 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213745 | TTGGACAGCTGGAGG[A/G]TTGACACCATGGACT | 56916 |
rs546085735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238044 | TTAATTTTTTCGAGG[C/T]TTAAAATATGTACAA | 56916 |
rs546127513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245552 | ACAGCAGACATAACA[C/T]AAGGACAGTGAGCTA | 56916 |
rs546258454 | snp | A/C | 0.000703977 | 0.0187481 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289723 | CACACGTGAAATTTC[A/C]AAAAAGAAGCCACAA | 56916 |
rs546309687 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270117 | TAGCATTTGCTAAAA[C/T]ATCAGTGAACATCAG | 56916 |
rs546342416 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233445 | TGAAATAAATATTCC[C/G]TGTTTGCTGAGGAAA | 56916 |
rs546346381 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283055 | CATGTGATAATGATT[A/G]TTTTCCATTTTAATT | 56916 |
rs546370891 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242327 | TGAGATTACAGGCGT[A/G]AGCCACCACGCCCGG | 56916 |
rs546398524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269583 | GATGTTTGAAAAATG[A/G]TATCTGTGCCTATGT | 56916 |
rs546475289 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260838 | CTTCCAAATGACCAT[A/T]ATTAATTTATGCTCT | 56916 |
rs546500898 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283538 | CATGAAGTATTAACA[A/G]TTGACGGCCGGGCGC | 56916 |
rs546543117 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266764 | ACAAGTTCTTCATGA[C/T]GAAGTTTACTTTGCT | 56916 |
rs546576030 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207906 | CAGCACGGCCTCCGC[C/T]GCTCCCCTTCTTTGG | 56916 |
rs546578975 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246879 | ATTGTTTCTGTTTGA[A/T]CTAATTGGGAAAGGG | 56916 |
rs546598177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94253716 | GAATTTGACTTTCTA[C/T]AAACAGGTTGTATAC | 56916 |
rs546609174 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213445 | CAGGAGGTTTTAGAC[A/C]ATATAGATGAAACTG | 56916 |
rs546612266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94253155 | TTTCATTGTAAGCCA[A/G]TAGTATTTCAAATAG | 56916 |
rs546643124 | snp | C/T | 0.000167126 | 0.00913976 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94290833 | CAAAGATTTGTTAAT[C/T]TTTGGAAATCATGCT | 56916 |
rs546672404 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215231 | AATGTTAATTGAAAA[A/G]CAATACTTAGTTAAA | 56916 |
rs546682618 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216553 | CATTGTCATGCAACT[A/G]TTCTCCAGCACTCTT | 56916 |
rs546703707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241690 | ATCCTGCCACCAGAC[A/G]GTTGACTGAATCTCC | 56916 |
rs546724493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285667 | TACTTTAATCTGTCT[A/G]CAGCGAGAGAGAAGT | 56916 |
rs546766147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240717 | TTACAGTGATTTCTA[C/T]TTCTGAAAGACTGCA | 56916 |
rs546833982 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220284 | ATGGAATTTTGCTTT[A/G]TTGCCCAGGCTGGAG | 56916 |
rs546841368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221751 | ATATGGGCTCTTTTG[A/G]CTGAATCTAGAAACC | 56916 |
rs546865233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214401 | TGAGTAGCTGGGACT[A/G]CAGGTGCCCGCCACC | 56916 |
rs546884586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234560 | GTCCTGCCAGTAGCA[C/T]TCTTGCTGAGAAATA | 56916 |
rs546909812 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261351 | AAACTCATAATATGC[C/T]TAGGCACTAACCTTC | 56916 |
rs546946483 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220905 | AAATGTGAAGTACGC[A/C]TCACTGCATACCGTA | 56916 |
rs546969883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261769 | CACGTGCCACCACAC[C/T]GGCTAATTTTTTGTA | 56916 |
rs546991518 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228562 | CTACTCAAAATACTG[A/G]TTTATAAATAAGGAA | 56916 |
rs547049096 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246195 | CATGATCCTGGCTCA[C/T]CGCAACCTCCGCCTC | 56916 |
rs547051597 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236517 | CCCTAGAAATTAAAA[A/G]AAAAGTAAATAGATG | 56916 |
rs547056157 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288004 | AAAATATATATATAT[A/T]TTTTTAATTGTTGAA | 56916 |
rs547068112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279484 | AATGATCTGGGGGAC[A/G]TAAAAACAAAGAAGG | 56916 |
rs547082132 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285136 | CTAATTAGTCAGTGC[A/C]AGAGGATGACAAAGA | 56916 |
rs547107106 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255643 | GTTTAGAGGTTACTA[A/C]CTTTCTATACTACTA | 56916 |
rs547150912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248992 | TTCCTATGCATGAAC[A/G]CAAGGAGTCTTTTCT | 56916 |
rs547178643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283680 | AATACAAAAAATTAG[C/T]CGGGCATGGTGGCGG | 56916 |
rs547212648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248270 | ATCAGTACTTCATTC[C/T]TTTTTATGACTTAGT | 56916 |
rs547244591 | snp | A/G | 0.000487052 | 0.0155977 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290304 | TGATTTCCCTCTCCC[A/G]GCTTTTGCTTCTCTT | 56916 |
rs547296671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256511 | GGGATTACAGGTGCC[C/T]GCCACCACACCTGGC | 56916 |
rs547310246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228300 | CTTTTCAGAATTACC[C/T]TTGTTAGCATTTTCC | 56916 |
rs547347755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277951 | TACTTCTTAATTCTC[C/T]AGAGTCACCAGTTCT | 56916 |
rs547368844 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286470 | AAGGGTAAGGATTCT[-/G]GGTGTGAACTAGCCT | 56916 |
rs547373397 | snp | A/T | 1.76658e-05 | 0.00297197 | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94278899 | TATCCGCTTGGTTTT[A/T]TTTTTTACTGTGTTC | 56916 |
rs547553322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223231 | CGGGCGTGGTAGCTC[A/G]CATCTGTAATCCCAG | 56916 |
rs547637961 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284613 | TTTTTTAAGTGGAGA[C/T]AGGGTTTTGTCATGT | 56916 |
rs547658709 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291637 | AACTTTATGCCAGTA[C/G]ATACTTACTTTGAAA | 56916 |
rs547669815 | in-del | -/A/AA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228254 | TTGTAGAAAAGTTGC[-/A/AA]AAAAAAAAATGCATT | 56916 |
rs547705481 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221261 | ATGTGTCGACCTTTG[A/G]AAGATGTGTATTACT | 56916 |
rs547749781 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250303 | AGAGTACATTTACAC[A/T]TGCACTGATTTATTT | 56916 |
rs547776343 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244506 | TATGAAAGACAGAAA[A/C]CATGTTCTAGGATTT | 56916 |
rs547798468 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219655 | ATGCTAATAATGTAA[C/G]TTCCCATTACCTTTG | 56916 |
rs547799681 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282592 | GATTGTCTTAATAAG[A/G]ACGGAATTGTGTAGT | 56916 |
rs547858841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245837 | CTGCAATTTTTAACA[A/G]TTTTGCATAATGCAG | 56916 |
rs547859910 | snp | A/G | | | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252341 | AGACATCATACAGAT[A/G]CGCAGCTGCCATTTG | 56916 |
rs547871121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213889 | GTCTAAACCCTAGAA[C/T]TTGGGACTCATCAAT | 56916 |
rs547913400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245118 | GAATTTGATACTTCA[A/G]AGAAATTTTAAAAGT | 56916 |
rs548017015 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252193 | CAACTTAGAATATTG[A/T]AGATAGTATTGGAAA | 56916 |
rs548022668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217461 | GTTGTTGTTGTTTTC[C/T]CTTTGACCTGAAAGT | 56916 |
rs548055650 | snp | A/G | | | intron-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94253425 | AAGAGCAATAGCAAC[A/G]GCCAGGGGAGCTCCA | 56916 |
rs548056969 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231810 | GGCCACTCCCCTTTT[C/G]TGCTTCTCTAAAGAG | 56916 |
rs548088097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280869 | GACTTGCTTGAATTA[A/G]CCTATGTCTGTTCTG | 56916 |
rs548096041 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210822 | GCCTGTAATCCCTGC[C/T]GCTCAGGAGGCTGAG | 56916 |
rs548153761 | in-del | -/CCAC | 0.0107246 | 0.0724382 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242286 | CTGACCTCAAGTGAT[-/CCAC]CCACCTCGGCTTCCC | 56916 |
rs548284006 | snp | C/G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259090 | TTTTAGCCTCCCTTG[C/G/T]GATCGTTTGACAAAG | 56916 |
rs548301906 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290503 | TAAAGGCAGCATTAG[A/G]TACTGCATGGAAATA | 56916 |
rs548358088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281312 | TAAGACATACGTCTT[C/T]GGTATTACTGATTTG | 56916 |
rs548435665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232888 | AGGAGGCTGAGGTGG[A/G]AGGATTGCTAGAGCC | 56916 |
rs548461633 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240507 | AAGGCCTGGTACATA[C/G]TAGACTCAGAAATTG | 56916 |
rs548474112 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239726 | TACAGGCATGCACCA[A/C]CACGCCTAGCTAATT | 56916 |
rs548475869 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277426 | ATTGATGAAGAGCTC[-/AG]ATATATAGTATGTGC | 56916 |
rs548546243 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283701 | ATGGTGGCGGGTGCC[C/T]GTAGTCCCAGCTACT | 56916 |
rs548565211 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282347 | GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 56916 |
rs548565505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282920 | TTGAAGTAAGAGTTG[A/G]TAGGGGTAGCAATAT | 56916 |
rs548584307 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255044 | AGGTTTGATAATGTA[A/C]CTCTAAACAACTTCA | 56916 |
rs548606599 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94290973 | CGGCTTAACCCCAGT[C/G]TTGATGGTATATTGA | 56916 |
rs548643680 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231956 | AACCTCTGCTTCCTG[A/G]GGTCAGATGATTCTC | 56916 |
rs548659865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220964 | AGCAATTGCTTTGTG[C/T]TAACCAGTCACGTTT | 56916 |
rs548698690 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227258 | ATAGTGTAAAGGATG[A/T]GATGAAGGAGGGGCT | 56916 |
rs548776245 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288939 | TCATTTAATTAAAAT[A/G]TAGGGCAAACATTGG | 56916 |
rs548784222 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271061 | ACATGTTGCAAACAT[A/T]AAAATACAAATTAAA | 56916 |
rs548859538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254015 | AACAAATCTAAATGA[A/G]CATTAAATGCCCTGA | 56916 |
rs548882179 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235311 | ATGTGATATTTTGTG[A/G]CTGGCTGCTTTCACC | 56916 |
rs548920523 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221550 | ATGAAATGAAAACAA[C/T]GTATTGCAACAGATT | 56916 |
rs548935122 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276815 | GTTACCTACTTATAA[A/G]AGAAGACCAATGGTT | 56916 |
rs548976719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216639 | ATTCCCCCAGCCCCC[A/G]GCAACTACCGTTTAC | 56916 |
rs548988143 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223229 | GCCGGGCGTGGTAGC[C/T]CACATCTGTAATCCC | 56916 |
rs549050622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210620 | GAAGGGCAGGGTTTA[A/G]ATCCCTGATGGGAAT | 56916 |
rs549060188 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234970 | GCAGGACATGGCCAT[G/T]TGAGCTGTCAGTGAT | 56916 |
rs549109616 | in-del | -/A | 0.125383 | 0.216727 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262937 | GGTAGTTGGTTACAG[-/A]AAAAAAAAAGTGTAT | 56916 |
rs549133133 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254612 | TTATGCATTACTTAC[C/T]TAAACCTCCTAACAT | 56916 |
rs549146336 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234282 | GACATTTATTTATTG[A/C]AAGTCTTAACTTTTT | 56916 |
rs549170607 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207969 | GCCCTGGCAGGTCCT[C/T]TCTCGAGGCAGGGGG | 56916 |
rs549209286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214466 | TAGAGACCCGGTTTC[A/G]CCGTATTAGCCAGGA | 56916 |
rs549253746 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249078 | AAGAAGGAAAAGTGA[A/G]ACTATGTATAGCCAC | 56916 |
rs549302222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94278787 | CTTGTACTGGGGATG[C/T]ATTTTGTTTAGTCAT | 56916 |
rs549386885 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208649 | GATGAAAGGCAGAAG[A/G]GATTCTCATTTTTAT | 56916 |
rs549404759 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225503 | TGACCTCAGTTAAAC[C/T]TTAATTACCTTTTTA | 56916 |
rs549408815 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223048 | AGAAAAACAAAGAAA[A/C]GGTCAATAAAGAGTC | 56916 |
rs549435779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243218 | TGCTGGGATTACAGG[C/T]GGCAGCCACTGTGCC | 56916 |
rs549448914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229298 | TGTGGTATACTAACC[A/G]GTGTTCTAGAACTTA | 56916 |
rs549541866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257260 | CTAAAATTGAAACAG[C/T]ATGTGCAGAAATGAA | 56916 |
rs549544371 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272006 | AAACAACAGAAATTT[G/T]TTCTTCACAATTCTG | 56916 |
rs549624230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230428 | TTTTGCAACTCCATA[A/G]TACTACATTGTGTGA | 56916 |
rs549667556 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236692 | CCTAGAAAATACTGT[A/T]TATATGTGATTGTGT | 56916 |
rs549681596 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269650 | TTTTAACCATTTGAA[C/G]TATTGTTTTCATTCT | 56916 |
rs549687404 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222682 | ATTTTAAAAATTGAG[A/G]CTGGGCTTGGTGGCT | 56916 |
rs549692751 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231059 | TGAGAACAGTTTCAC[C/T]GAGTTGTTGTGCGAA | 56916 |
rs549725540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94263958 | TGATATAGCTTTTAC[A/G]TATGAAGTATTCAGT | 56916 |
rs549751045 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287901 | TTCATGCTTATAATG[A/C]CAGCACTTGGGGAGA | 56916 |
rs549760640 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273385 | TGTATTGTATATGAA[C/G]TAGCAATGAAGATCT | 56916 |
rs549804245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279951 | CTCACTGCACCCTCC[A/G]CCTCCCAGGTTCAAG | 56916 |
rs549961622 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282343 | CCTCGTGATCCGCCC[A/G]CCTCGGCCTCCCAAA | 56916 |
rs550023371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279541 | AAACTATGGCCTTAC[A/G]GCAGTGACTATTTTT | 56916 |
rs550063294 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286132 | CATTTCCTCAGAGGG[A/C]AATTTTTCAACCTCC | 56916 |
rs550102575 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94251085 | GTCTTTCTTAATAGT[G/T]AAGGCTACTTTTAAA | 56916 |
rs550187990 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245216 | AGAAGTTTCTAGGGT[A/C]CTGTCCTGATGATCT | 56916 |
rs550241941 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207895 | CGGATGCCCGCCAGC[A/G]CGGCCTCCGCCGCTC | 56916 |
rs550245770 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247072 | ACATTGGGATGGGAT[A/G]GTGGTGTCAATATCT | 56916 |
rs550342430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231864 | CAGATTTTTCTTTTT[C/T]TTTCCTTTTTCTTTT | 56916 |
rs550361803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218896 | GGCTCACTGCAACCT[C/T]TGTCTCCTGGGTTCA | 56916 |
rs550381696 | in-del | -/CAA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221303 | TATTTTCCAAATGAC[-/CAA]AGCACAGTATTAGGA | 56916 |
rs550409669 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211781 | AGACTCTTCCTGCTG[A/G]TATTTGCATATGACT | 56916 |
rs550435105 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224188 | GTTTGCTCAACTTGC[A/G]TGCAATGTTTATAAA | 56916 |
rs550448995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246426 | GCCCAGCCATAACTG[A/G]CAATCTTAAGAGGTA | 56916 |
rs550500314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268800 | TGGATTAAATGAAAT[A/G]ATAATGTATATTAAG | 56916 |
rs550558256 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214071 | TCCTGTAGAGAAGTC[A/C]AGTTGAGTGGGGACT | 56916 |
rs550617708 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260593 | CCACCTGCCTCGGCC[C/T]CAAAAGTGCTGAGAT | 56916 |
rs550631361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246836 | GAAGACTGAAGGTAT[A/G]TCATTAAACCTGCCA | 56916 |
rs550632937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219818 | TTACTCATGAACATG[A/G]CTACTTCACTCCTAT | 56916 |
rs550692325 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222920 | AGGGAGCTGAGATTG[C/T]GCCACTGCACTCCAG | 56916 |
rs550719889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221063 | CAAAATGAACAAAGT[A/G]ATACAAAGAAAACAA | 56916 |
rs550815722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226051 | AGATTTTAGCACATG[A/G]TTATAACTAACAACA | 56916 |
rs550818828 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233891 | TATACACATAGACAC[A/T]ATAATGAAATAACAT | 56916 |
rs550886954 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269498 | GGCAAATTAAGTTTT[G/T]TTTTTTTTTTTATCT | 56916 |
rs550906589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233368 | TGTCTTTTATAAAGG[A/G]TAAACATATGAAGTT | 56916 |
rs550927376 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226554 | ATTTTGAGAGCAGAT[A/G]CTTAATTTCCTTATT | 56916 |
rs550927522 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260131 | ATTATACCTCCCCAG[G/T]GTAGTTTAACATGTT | 56916 |
rs550952306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271174 | CAGATGTTGTGTATG[C/T]ACATGTGTACGTACA | 56916 |
rs550975453 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239395 | GACAGTATCATCCTG[C/T]GTATTAAACACTAGG | 56916 |
rs550985971 | in-del | -/TGTT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223023 | TTTTGTACTACAGTC[-/TGTT]TAAGGGAGAAAAACA | 56916 |
rs551007082 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277234 | TTCTGTTAGGTCTCT[G/T]TTGTTGTTTTCATAG | 56916 |
rs551047613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224937 | CCTTTGAACTAAAGA[C/T]TCAACTGGTCATTGC | 56916 |
rs551059512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242899 | CCAGCCTGGGTGACA[C/T]AGTGAGACCTGTCTC | 56916 |
rs551084920 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250311 | TTTACACTTGCACTG[A/G]TTTATTTGAGTATAT | 56916 |
rs551087192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262292 | TTTTAATCTCAATAG[A/G]TGGTACCACTAATCT | 56916 |
rs551120993 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247671 | GCTATACCCATTAAG[C/T]AGTTTCTCCCCATTC | 56916 |
rs551122300 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240659 | ATCAATTTAGAGATG[C/T]ATATTTTTAGATTAA | 56916 |
rs551154314 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261889 | TGCTGGGATTATTGG[G/T]GTGAGCCACCACAAC | 56916 |
rs551171531 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237214 | TTACTGCTTTTCTAC[C/G]AATCAAATCTTGTAA | 56916 |
rs551181058 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254897 | TAAATGTGATTTATT[A/T]ATAGAGTACTTTTTT | 56916 |
rs551183968 | in-del | -/TTTA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249913 | AGTATTTTCATACTG[-/TTTA]TTTATGTTGTTTATT | 56916 |
rs551202975 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289656 | TAATTTCCATATTAC[A/G]TTTCTCATAGTATGG | 56916 |
rs551235548 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213650 | AGGCAACTGAGGGGA[G/T]TTGTAAATGATACGC | 56916 |
rs551269444 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276709 | CCCTTTAAAAAATTA[G/T]TAGGTCATAAGCCAT | 56916 |
rs551307392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248165 | CATCTGTGTTGCTGC[A/G]AAGAACATGATTTTG | 56916 |
rs551308404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94263402 | CCTGAAAAGCACAAA[A/G]TAGGGGGAGTAGGAG | 56916 |
rs551410727 | snp | A/G | | | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206726 | GCATCCCAGGTTCAA[A/G]CTATTCTCCTGCCTC | 56916 |
rs551451353 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229447 | TTAGTACTATTATTA[C/T]TCATTTTGGTGCACA | 56916 |
rs551492828 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210748 | AGACCAGCCTGGCCA[A/G]CATAGTGAAACCCCG | 56916 |
rs551544785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228825 | TGTCATATCTCTTTA[A/G]ACTCATTTAATCTGA | 56916 |
rs551576763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209192 | ATTTCCACTCGAATC[C/T]ATGTTCATTGAACAG | 56916 |
rs551611840 | snp | A/G | 1.66471e-05 | 0.00288501 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208595 | AACAGGTGAGTTACA[A/G]TGTTAAAATTGATGT | 56916 |
rs551626721 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231182 | TTGTTTGTTTTTTTT[C/G]TTGCTGCTGTGTCCA | 56916 |
rs551636130 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242296 | GTGATCCACCCACCT[C/G]GGCTTCCCAAAGTGC | 56916 |
rs551757236 | snp | A/C/G | 0.000182161 | 0.00954199 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249766 | AACAGGTGAGTAGTC[A/C/G]TGTATGAAAATTTAA | 56916 |
rs551783190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217426 | TATATATGATGTATC[C/T]TAGATTTTGATGTGT | 56916 |
rs551809316 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285527 | AATTAATTGGAAATA[A/T]GCAAGTTTTTTCATT | 56916 |
rs551836144 | snp | C/T | 6.60971e-05 | 0.00574841 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237046 | TAATTTTAAGCCATG[C/T]CGATTTATTGTTACG | 56916 |
rs551896016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243892 | GTTCAAAAATGCCAC[A/G]CAGTACATGCAGAGG | 56916 |
rs551901993 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268444 | CTTGGCTGCATTTAT[A/G]AGTGATGTATGCCTA | 56916 |
rs551908285 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234236 | TACGTTTGAAGATAT[A/T]AACTATTAAATCTAA | 56916 |
rs551948099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250256 | GTTTAATCCCATGAT[C/T]ATATATAGAAGCACA | 56916 |
rs551958914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272546 | TACCACTATTCTTAT[A/G]CCTATCCTCGTGGAT | 56916 |
rs551973186 | in-del | -/CTC | 0.00438332 | 0.0466095 | intron-variant, cds-indel, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94266156 | ATCAGCAAATTTCAT[-/CTC]CTAAAAGTGTAGTTG | 56916 |
rs551977247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212573 | CTCACTGCAACCTCT[A/G]CCTCCTGGGTTCAAG | 56916 |
rs552006648 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224583 | CAAAAGATTTCAGAT[G/T]TTAGAACATTTTTTA | 56916 |
rs552015679 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219010 | AGGGACAGGGTTTCA[A/C]CATGTTGGCCAGGCT | 56916 |
rs552017217 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242175 | AGTATCTGGGATTAC[A/G]GGAGTGCAGCACCAC | 56916 |
rs552041138 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210228 | TGCTTTAGGAATTAC[A/G]TGATCAGCCTTGATG | 56916 |
rs552056847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237474 | AAATAAATGCTGACT[C/T]GATTTTTTTTAACTT | 56916 |
rs552080362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216696 | CTAAGTATCTCATTA[A/G]AGTGGAATCATCACT | 56916 |
rs552114659 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258304 | GGATTACAGGCGTCT[A/G]CCACCACACCCGGTT | 56916 |
rs552132290 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286213 | AAATGAAGGAGGGAG[G/T]TTTGTTCTCTTATTT | 56916 |
rs552136802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275845 | TCTGTCCCCCAGGCT[A/G]GAGTGCAGTGGCGCG | 56916 |
rs552165825 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234349 | ATTAAAGCCTTAATA[A/G]CGAACATAGGTTGTG | 56916 |
rs552378179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94251354 | TGTTTAGTAACATAC[C/T]TAAGGAAGAATCAAG | 56916 |
rs552382646 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280099 | CGAACTCCTGACCTT[A/T]GGTGATTTACCCACC | 56916 |
rs552516141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239664 | TACGACCTCTGCCTC[C/T]CAGGCTCAAGTGATC | 56916 |
rs552526367 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282254 | GGCGCCTGCTACCAC[A/G]CCCGGCTAATTTTTT | 56916 |
rs552537461 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239642 | CAGTGGTGCGGTCTC[A/G]GCTCACTACGACCTC | 56916 |
rs552580359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239199 | AATGACAGGTTTGTC[C/T]AACCTTGAAGATAAG | 56916 |
rs552585980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288731 | TTATTCATAGTTACA[A/G]ATCTATCACAGATCA | 56916 |
rs552597348 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255668 | CTACTATGACTTATT[G/T]GTCAGATAATTATGC | 56916 |
rs552614115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226973 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCGTTAG | 56916 |
rs552681080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232809 | GGGAAACATGGCAAA[A/G]CCCTGTCTGTACAAA | 56916 |
rs552682237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232663 | GAAGCTTTTGAAATA[C/T]GTACACTGGCTAGGC | 56916 |
rs552703723 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206458 | AAAACAATTGAACGT[A/G]TGAGAAACGGTAGAA | 56916 |
rs552725284 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286929 | GAGTGCAGAGGCGCA[A/G]TCTCCGCGCACTGCA | 56916 |
rs552761666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259921 | TGTCTCATAAATGCC[A/G]TAGTGTTTGTTCATT | 56916 |
rs552781545 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291230 | CTCTAATGAAATGTA[C/G]TTGGGTTCTTCCTGT | 56916 |
rs552805540 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94205768 | GCCTCCCAAAGTGCT[A/G]GGATAACAGACGTGA | 56916 |
rs552893941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239889 | TGTTCTGTTCTTTTT[A/G]GGAAAGAATTCAGCA | 56916 |
rs552900277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247208 | GTCAGGGAACTGATA[C/T]AGTATGGGATTTCTG | 56916 |
rs552909309 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206160 | TATGCAAAAGAAAGG[A/C]AATCAGTGTATCGAA | 56916 |
rs552912102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282478 | AGTCTAAAACACCTT[A/G]TCTTTCATCAAGATT | 56916 |
rs552945864 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288281 | ATGTCTTTTATAGCT[A/T]TCCTTAAAACACTAG | 56916 |
rs552963520 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239876 | TGCACCTGGCTTCTG[G/T]TCTGTTCTTTTTAGG | 56916 |
rs552975333 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289079 | GATGAAAAATAAGAA[G/T]ATAGATTGGTTTTCG | 56916 |
rs552986911 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94263234 | CACATTTCAATGTAT[C/T]ACACACACATACTAC | 56916 |
rs553025175 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241845 | CTCAAGCCCAGTTGC[C/T]ATGGCCATTTGTAAA | 56916 |
rs553034569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232975 | ACAGAGTGGAACCCC[A/G]TCTCAAAAAAAGAAA | 56916 |
rs553044061 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254963 | TAATAAAATTATCAA[A/G]AGTCAATATTATGCA | 56916 |
rs553090314 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247773 | ATTTAGGTGGAATTA[A/T]ATAATATGTAACCTT | 56916 |
rs553121067 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230022 | GAGGGTATACAGTCA[A/G]TGCACTTGGATTATT | 56916 |
rs553129323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220687 | ATTGATATTTGCACT[C/T]ATGGTGCAAAAGCAA | 56916 |
rs553141303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260245 | CTTTCATCAGAAGAC[A/G]GTAATATCTGATTGT | 56916 |
rs553203279 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211600 | AATTGTATGTAGTCA[A/G]AATTACCTGTAATCA | 56916 |
rs553205623 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290448 | AGAACAGATTACTTA[A/G]AGCTATTTCATTTCA | 56916 |
rs553221830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208668 | TCTCATTTTTATTCT[C/T]GATGTCATATATATT | 56916 |
rs553230366 | in-del | -/AT | 0.00478085 | 0.0486577 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230386 | TATCTCCTGGAAATC[-/AT]ATCAGTTCTAGAAAT | 56916 |
rs553245873 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207555 | GCGCGCGCCTCGACA[C/T]TGTCGGCTCGCGCGT | 56916 |
rs553257777 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206889 | TCAGCCCCCCAAAGT[G/T]CTGGGATTACAGGCG | 56916 |
rs553258651 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256563 | AGATGGAGTTTCACC[A/G]TGTTGGCCAGGCTGG | 56916 |
rs553280931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261089 | TCAGAGTTACCTCTC[A/G]TGTAACACAGCTTTT | 56916 |
rs553345863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264303 | ATCAGATTTGCAGTG[A/G]CTACATTTGATACTA | 56916 |
rs553349636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208107 | GTCAGCTCGTGGTTT[C/T]AGTAAGGAGGGGCGG | 56916 |
rs553365202 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276886 | TTAAATTACTATATC[A/T]TTTATCACAGAATGT | 56916 |
rs553428994 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214323 | GCTGGAGTGCAGTGG[C/T]GCAATCTCAACTCAC | 56916 |
rs553608095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276798 | GTGATACGAGGACAC[A/G]AGTTACCTACTTATA | 56916 |
rs553613708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271665 | ATAGAAAAGTGAATA[A/G]TATTCACAGGATTTC | 56916 |
rs553664737 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284258 | CGTGAAGCCGGGAGG[C/T]GGAGCTTGCAGTGAG | 56916 |
rs553750609 | snp | C/G | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278296 | AGTGCCATCTAGAAT[C/G]AATCAAGTTTCTGCA | 56916 |
rs553772398 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283809 | CCAGCCTGGGCGACA[A/G]AGCAAGACTCCATCT | 56916 |
rs553784345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94209601 | GCCACCCTTCTACTT[A/G]AATGTAATAATGATG | 56916 |
rs553837603 | snp | A/G | | | intron-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94253490 | CACCACAAAAGAAGC[A/G]ATTGTTTATTTTCTT | 56916 |
rs553908610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277704 | CTCCCAGTTTTTTCA[A/G]TACCGCAGTGTTTAC | 56916 |
rs553920687 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234472 | TGACAAGGGTTTTTA[G/T]TGGCATTTAGTGCCC | 56916 |
rs553937734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224143 | GTTTATGGCAATTAA[C/T]ATGGATGTGATTTAT | 56916 |
rs553950362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216354 | GATTTTTATGTGGTC[A/G]CCTTGTTCATCCTTT | 56916 |
rs554004453 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255872 | ACTTACAGTTTTTCT[A/G]CATAATAGCAGTAAT | 56916 |
rs554021770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230695 | GCAAAACTACCCCCT[A/G]CCCCAACTTTGAGAA | 56916 |
rs554023724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249252 | TCTTCTCAGAATTTG[A/G]AATTTATAGGTGGAT | 56916 |
rs554068796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222080 | CTGGTGATAAGGGCT[A/G]TATATTTGCCCTGGT | 56916 |
rs554084456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228419 | ACAAGGTCATTCATT[C/T]ATTTGCATATTAACA | 56916 |
rs554085524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256788 | ATTTGTAAGATTACT[A/G]TATATTCAGGCTTTG | 56916 |
rs554121326 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230047 | ATTATTAATTAATTA[A/T]TTTAAATGTTTTGTT | 56916 |
rs554240416 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223818 | GAACTCCTGACCTTG[G/T]GATCCGCCCACCTCG | 56916 |
rs554270882 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273562 | CTTCTGTATTTTTAT[G/T]TATTTATTTTTTGTT | 56916 |
rs554284021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245348 | CAGTGTAATACAAAT[A/G]ATCAGATGTTTTAAA | 56916 |
rs554285774 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250490 | AAAACATTTCTTGAT[A/C]CTCTAGTGTTCACAG | 56916 |
rs554286030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237818 | TTCATTATTATAGCA[C/T]TAAAGTAAATGTCCT | 56916 |
rs554365759 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217910 | GCTGCTCACATTTTC[A/T]TTCAGTTACACTTGC | 56916 |
rs554396907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284913 | TTTACATATATCCAA[A/G]TAACTATATTTAGTA | 56916 |
rs554440905 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278255 | GAGCTTCAAGAAGTA[-/C]ATGGCAGCCCAGAAT | 56916 |
rs554441380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212070 | TTTATCTCCATTGTT[C/T]AGGGCAACGACTGGC | 56916 |
rs554478378 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211295 | ATAAATAAATAAGAA[A/T]AAAAATCAAAGGTCC | 56916 |
rs554478432 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218433 | GAGTAGCTGGTACCA[C/G]AGGCATGCATCACGA | 56916 |
rs554531667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269631 | AGTGATAACTGTTAA[C/T]AGTTTTTAACCATTT | 56916 |
rs554545010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243405 | TACCATTTCTACTTG[A/G]TGATGGGTTGCTGCT | 56916 |
rs554598388 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258480 | CTGTCAGTTTCATCT[C/G]TTTTAGAAAATCAGG | 56916 |
rs554641357 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256630 | GGCCTCTCCAAGTGC[C/T]GGGGTTACAGGCGTG | 56916 |
rs554655804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287441 | CCTCTTACATGAAAC[C/T]ATGAAAGGTAAAGAC | 56916 |
rs554674377 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260929 | GTGTAAATTGGTACA[C/G]CTTAAGTGAATTTGT | 56916 |
rs554683678 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228784 | AGTACTTTATGGTAA[-/T]TTTTTTTTTTACAGT | 56916 |
rs554684423 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222461 | CCCCAACATTATACT[A/G]TTTCCTCTGTTAATC | 56916 |
rs554700515 | in-del | -/TT | 0.481396 | 0.0946345 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226508 | TCTGGATAACAGTGA[-/TT]TTTTTTTTTTTTTTT | 56916 |
rs554702657 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259539 | GTGTTAAGGGGTCCT[A/G]AGGAGTTGTTCTGAA | 56916 |
rs554707301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239320 | TAAGTGATCTTTAAC[A/G]GATCCAGAAATTGTG | 56916 |
rs554729407 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286903 | AGAGTCTTGCTCTGT[C/T]GCCCAGACTGGAGTG | 56916 |
rs554761299 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206922 | AGCCACCACTCCCAG[C/T]TTATTGTACATTTTT | 56916 |
rs554773274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224659 | AGCTCGTGAGCCCTA[A/G]TAATGATTGTTATAA | 56916 |
rs554776629 | in-del | -/TTG | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281680 | ACAATTGATAGTATT[-/TTG]TTGTTTTTATGTTTG | 56916 |
rs554794169 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252480 | ATTTTTAAAGTGTAT[C/G]AAATTTAACAATAAA | 56916 |
rs554805077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266346 | AGTCCTGTTACTTGT[A/G]AATAGTTTGATCAGG | 56916 |
rs554818066 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222226 | GGTTTGGCATATTTT[-/G]GAAATGACATGTTTT | 56916 |
rs554903530 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227033 | TGGTTTCTAAAGAGC[A/G]TGGTCAGAAAAGCCT | 56916 |
rs554904312 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281116 | AGTAATGCTGCCGTT[G/T]ATGTGTGAAATAGCC | 56916 |
rs554908632 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284554 | AGGTGTGTGCCACCA[C/T]ACCCAGCTAATTTTG | 56916 |
rs554912327 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284034 | GCACTGTAAAGAGGT[A/G]AAGATAGCCGGGCAC | 56916 |
rs554992600 | snp | C/G | 2.13108e-05 | 0.00326419 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283100 | TTTAGTGAGATTTAA[C/G]CTAATTTGTTTATCT | 56916 |
rs555028031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220006 | TCCTCTGTTTTTGTA[A/G]TTTTCCTTTTTGCTT | 56916 |
rs555096418 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219384 | TCTCCCACTAGTGAT[G/T]TTTTTTGTTCGAATG | 56916 |
rs555099654 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214257 | TATTGAAAATTGAGC[A/G]TTCTTTTGTTTTTTT | 56916 |
rs555127702 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267652 | AAAACAATAACTTCA[A/G]AATAGCCTGTTGCCT | 56916 |
rs555131203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228325 | TTTTCCCACAATTGC[A/G]TTATCACTCTTCGTA | 56916 |
rs555133714 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277409 | AAGGATGACGATTTT[A/G]AATTGATGAAGAGCT | 56916 |
rs555136363 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220438 | TTTTTAGTAGACACA[C/G]GGTTTCACCACATTA | 56916 |
rs555136611 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213645 | AGAGGAGGCAACTGA[A/G]GGGAGTTGTAAATGA | 56916 |
rs555203609 | snp | C/G/T | 5.01688e-05 | 0.00500822 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226133 | GAAGATTCTAGTGTT[C/G/T]CAGAAACTCCAGATA | 56916 |
rs555204593 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289824 | TGTTTGTAACAAATA[C/T]GCTAATGCTTTAGAA | 56916 |
rs555209721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275943 | GCTGGGACTACAGGC[A/G]CCCACCACCACACCC | 56916 |
rs555263242 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219407 | TTCGAATGAGCCTTA[A/G]TCTCCTACTAGTGAT | 56916 |
rs555265972 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289215 | GATCCAGTGTATTAC[A/C]GTGTATTTTTATATA | 56916 |
rs555288811 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246061 | TACCTTGTATTGCAC[A/T]CTGGACCTGGTACAG | 56916 |
rs555291375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232557 | ATTGTCCTCAAATAT[C/T]TGAAGGACAGGCATA | 56916 |
rs555335477 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282693 | ATTAGACTAAAGGTA[A/G]AAGTAATGTTTTTTT | 56916 |
rs555384150 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235344 | GTGGAAAAGATTCGT[C/T]GCTGTTGCAGGATGT | 56916 |
rs555385892 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269019 | CAGCAAAAGAATTGT[-/A]AAGACAGAATTAGAA | 56916 |
rs555387508 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217572 | TTAACATTTACTTCT[A/G]ATTTCACTGTTTTGT | 56916 |
rs555411591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235407 | GAAAGATAAAAATAA[A/G]CATGCTATTCAAGCC | 56916 |
rs555417023 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246938 | CATAGCCATATTGAT[G/T]TGCTCCAGCAAAAAT | 56916 |
rs555474021 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270662 | GTTTTTATGTGCATT[G/T]TAATAACTAATAGAA | 56916 |
rs555484935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227738 | GAGAACACTCCTAGA[C/T]GTCTAAATGGAGATG | 56916 |
rs555493004 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246601 | GACTACACTCCCACG[A/G]AAGTGGTGGGCCTCA | 56916 |
rs555554618 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222005 | TAAAACTGGTGGAAG[A/G]TAAGTGTTACTTTGG | 56916 |
rs555565727 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214570 | CGCACCTGGCCAAGC[A/G]TTTGTTAACCAAGGA | 56916 |
rs555635233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208794 | ACTTTTATATGAGTT[C/T]TTCGAATATGGCCCC | 56916 |
rs555679685 | snp | A/G | 1.96184e-05 | 0.0031319 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241041 | ACAGTATCAAAATTG[A/G]CTGCTTAAGGTTAGG | 56916 |
rs555706882 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221941 | CAAAGGGGATCTGGC[A/C]ATGGGCAGCAAACTT | 56916 |
rs555737756 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265926 | GATTTTATTTACTTC[C/T]GATATTTTTCTAAGT | 56916 |
rs555814307 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255798 | TCAGCTTTATAATCA[A/T]TTATTAGTCAAAATT | 56916 |
rs555891769 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275051 | GTACTATGTAGGAAA[C/G]TTTATGCTGTTAACT | 56916 |
rs555897154 | in-del | -/TGAT | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94290926 | ATAAAACTCTTACAG[-/TGAT]TATTTAGATATTAAA | 56916 |
rs555907484 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236090 | GTGAAATAGTTCTAA[G/T]CTTGCTAAGAATATG | 56916 |
rs555923894 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229053 | ATGTGTCAGGAGACA[A/C]ATGATATCCATTTGT | 56916 |
rs556000117 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261853 | AGGCTCAAACAGTGC[C/T]CTTGCCTTGGCCTCC | 56916 |
rs556124963 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255069 | ACTTCAAAAGGAAAC[A/G]AAAGCCAAAAAAATT | 56916 |
rs556156088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272709 | TTTTTTAAATTGCCA[C/T]GTGGTATGGTAGTCC | 56916 |
rs556224387 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281914 | AGGTGTGGTGGTGCA[C/T]GCCTGTGGTCCCAAC | 56916 |
rs556255832 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217718 | ATCTAAGTACAGATT[G/T]AATTATATGTCGAAT | 56916 |
rs556270584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274390 | GAGTGTGGTGGCTCA[A/G]TCTTGGCTCACCGCA | 56916 |
rs556275903 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223481 | CTGGGCGACAGAGCG[A/T]GACTCTGTCTCAAAA | 56916 |
rs556287814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210912 | GCACTCCAGCCTGGG[A/G]GACAGAGACTGTATC | 56916 |
rs556303779 | in-del | -/CT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268512 | ATGTGAATAGGATGA[-/CT]AAAGAATTGGGAAGG | 56916 |
rs556330788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210409 | TGTAAGTATTAGATA[C/T]CCATTGAAGAACTTA | 56916 |
rs556400058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286528 | CTTTTACTTTATTAT[C/T]GAAAATCAGTTTCCA | 56916 |
rs556400308 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279727 | TCCTAGTCTAGACTT[C/T]CATAATGCACTTCTT | 56916 |
rs556446529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284677 | GCCTCAAGCAATCCA[C/T]CTGCCTCAGCCTCCC | 56916 |
rs556462355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285760 | CTTGGGGAGGTGGGC[A/G]GTAGAGAAAGTTTGA | 56916 |
rs556550475 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206812 | TGTATATTTAGCAGA[A/G]ACGGAGTTTCACCAT | 56916 |
rs556595099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275213 | GTTATTGAAAAAAGT[C/T]GTCTTGTAATAGTAA | 56916 |
rs556632212 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246047 | CCCAAGTGGCGGAGT[A/G]CCTTGTATTGCACTC | 56916 |
rs556636805 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216246 | CTCCTAATACCATTA[C/T]CATAATGGTTAAGAT | 56916 |
rs556641174 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238529 | CTTCCTCATTATTTC[A/G]TCCCTAGCACTTACT | 56916 |
rs556646307 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278124 | TGAGAGTTATCTAGG[-/T]TAATCGATACATGAC | 56916 |
rs556695373 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247696 | CCATTCCCTCCTCCC[C/T]CTAACCCCTGGCAAC | 56916 |
rs556758177 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212201 | ATTTGTTTTTAGACA[A/G]TCTCACTGTGTGGCC | 56916 |
rs556786172 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261067 | AGATCACAATATGCT[A/G]ATTTTTTCAGAGTTA | 56916 |
rs556835840 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94205938 | GAGTAGGTAGGACTA[C/T]AGGCGCCCGCCACCA | 56916 |
rs556858599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244540 | GCTCCTAAAGGTAAC[A/G]TAACTGTGATATTTG | 56916 |
rs556877332 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237597 | ACCCTTAAATTATAA[A/C]CACCTTTTATGTCAT | 56916 |
rs556930290 | in-del | -/TATT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218710 | TTGTCTTTTCTAGGG[-/TATT]TATTAGAGAGTTTGA | 56916 |
rs556931646 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94253305 | GAAGAAGAAATTAGA[C/G]CTTACATTTAGGAAG | 56916 |
rs556940736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237265 | TATTTTCTCTCTTTT[C/T]AAAGTATAATTTCTA | 56916 |
rs557012049 | snp | A/C | 3.30945e-05 | 0.0040677 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208583 | TATAACTGAAAAAAC[A/C]GGTGAGTTACAATGT | 56916 |
rs557018033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252296 | TTCTTCAGTGTTGGC[A/G]TAGTTGAGTGGGGCT | 56916 |
rs557020471 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286848 | TAGCTTTGAAGTGTT[C/T]AGTTATGAAGAATCC | 56916 |
rs557062163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239386 | GTCTTAACAGACAGT[A/G]TCATCCTGCGTATTA | 56916 |
rs557071930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261703 | CAACCTCTGACTCCC[A/G]GGCTCAAGCCATCGT | 56916 |
rs557113685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232944 | AAGATGGCACCACTG[C/T]ACACCAGTCTGGGTG | 56916 |
rs557114141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288134 | ATTGTAAACATGGCA[A/G]TTTATTTTCAATATC | 56916 |
rs557206694 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246688 | ACCATTGAAAATACC[C/G]ACTACCTGTATCAAG | 56916 |
rs557208548 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214489 | AGCCAGGATGGTCTC[A/C]ATCTCCTGACTTGAG | 56916 |
rs557227048 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234920 | ACTATAGAGTACATA[C/T]TCTTTTTTAAAGGGG | 56916 |
rs557286439 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211030 | GTAATCCCAGCACTT[C/T]GGGAGGCTGAGGCGG | 56916 |
rs557291570 | in-del | -/AAATAT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221623 | ACCAGAGATTTTGAC[-/AAATAT]AAAACAGTGTCATCT | 56916 |
rs557317290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275960 | CCACCACCACACCCG[A/G]CTAATTTTTTATATT | 56916 |
rs557326733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94251774 | CCTTCATTCACAGGC[A/G]TCTTAGAATTCTGTA | 56916 |
rs557345815 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214271 | CGTTCTTTTGTTTTT[G/T]TTTTTTTTTTTGAGA | 56916 |
rs557375229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277487 | CAAAATTGGCTACGT[A/G]AATTAGTAACATTTC | 56916 |
rs557411026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220096 | TTGCAGCAGGAATAT[C/T]TTTTTAGCCATTGGC | 56916 |
rs557489481 | snp | A/G | 0.000251731 | 0.0112161 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208061 | GGGGAACGTGCCTGC[A/G]CGTGCTTGGGTAAGA | 56916 |
rs557496247 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241323 | GTGACTGTTTTTGCT[C/T]TCTTTTAAATTTATC | 56916 |
rs557504008 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239631 | AGGCTGGAGTGCAGT[A/G]GTGCGGTCTCAGCTC | 56916 |
rs557524519 | snp | A/C | 0.00279162 | 0.0372561 | upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207665 | GTCCCGGCACGGCTA[A/C]CGTCGCCCCACGCTA | 56916 |
rs557537631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272060 | GTATCGGTAGCTTGC[A/G]TTTCTCCTGAGTCCT | 56916 |
rs557552914 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247059 | AAGGAGGCATCTTAC[A/C]TTGGGATGGGATGGT | 56916 |
rs557559221 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242892 | CTGCACTCCAGCCTG[A/G]GTGACACAGTGAGAC | 56916 |
rs557589842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283769 | GGCAGAGCTTGCAGT[A/G]AGCCGAGATCACCAC | 56916 |
rs557590896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220538 | CAGGCATGAGCCACC[A/G]TGTCCAGCCCTCATC | 56916 |
rs557607288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269725 | CCAGGCTGAAGTGCA[A/G]TGGCATGATCTCAGC | 56916 |
rs557628513 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218964 | TTACAGATGTGCACC[A/G]CCACGCCTGGCTAAT | 56916 |
rs557634221 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282395 | GCCACCGCGCCCGGC[A/G]CAAATACGTTTTGAA | 56916 |
rs557687444 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271998 | AGTGGCTTAAACAAC[A/G]GAAATTTGTTCTTCA | 56916 |
rs557717664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271478 | ATATTTAAAATGAGT[C/T]ATGTTCAGCAAAGAA | 56916 |
rs557791618 | in-del | -/TG | 0.00358779 | 0.0422022 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94263584 | TATATTGCTATAAAC[-/TG]TATTTTATTTAGTTA | 56916 |
rs557807286 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262811 | GAAATTGTTACTTGT[A/G]TTTCCCAATGTTCGT | 56916 |
rs557813611 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241815 | AGTCTTACCTTGTTG[A/C]CTTGCATGCACAGAC | 56916 |
rs557899513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271106 | GTCACCTGTAATTCT[A/G]CCACTTAAACAAGAA | 56916 |
rs557926910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221982 | CACTAGGAGACATAT[A/G]GGGGGTGTAAAACTG | 56916 |
rs557948997 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215946 | GTAAGTATATCTTAA[A/G]TTCCACGTGTCTTAG | 56916 |
rs557957548 | in-del | -/TG | | | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289544 | CTGTGAAATAAGAAC[-/TG]TGAACTCTCAATTGA | 56916 |
rs557964859 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290207 | AAGCCCCTACCTTGC[C/T]CCATGGATTAATTCC | 56916 |
rs558015986 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236309 | AAAAATAGGGGATTT[A/T]AGTTTCTTCTGAAAT | 56916 |
rs558030498 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213831 | ACCCATCCTATTTTA[G/T]TACCAAGGTAGTAGA | 56916 |
rs558075397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264125 | TTGATTCATGTGATA[C/T]CTCTCCGTGTGATAG | 56916 |
rs558083660 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216271 | TAAGATTTCAACATA[C/T]CGTTTTGGGGAGTGG | 56916 |
rs558088443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233732 | TTTCCATCCCAGCTC[A/G]GGGTTGAGATTTTTT | 56916 |
rs558122872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235552 | CCAGATCATTTTGAT[A/G]CCATCTTACTATTAG | 56916 |
rs558165914 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266752 | TCTCTAAACAGAACA[A/T]GTTCTTCATGACGAA | 56916 |
rs558175933 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284437 | TTTGAGACAGAGCCT[A/C]ACTCTGGCTGGAGTG | 56916 |
rs558203207 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249187 | TATGTTGTGACTGAA[C/G]AATTAATATTTAAGC | 56916 |
rs558241669 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94279198 | AGGTCTGGTTCTGTT[C/G]CCAAGGCAGGCAGTC | 56916 |
rs558265486 | in-del | -/TTTCTCCTATATGACT | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224757 | GGATTTCAGATCTAC[-/TTTCTCCTATATGACT]TTGGGCAAGTTGCTT | 56916 |
rs558268778 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250445 | TTTGTAAAAGCCTAG[C/G]TGCATATTGAAATTT | 56916 |
rs558285857 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211131 | TATAAAATTAGCTGG[C/G]CATGGTGGTACATGC | 56916 |
rs558384310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255928 | CATCATTAAATCAAG[C/T]AGGGTTCAGAAATAC | 56916 |
rs558485283 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232196 | TGACATTATTTATTT[A/T]CTATCACTTGTATTT | 56916 |
rs558532337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275398 | TAATAATACTACTTG[A/G]TAATAATTGATGTAA | 56916 |
rs558543431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266023 | AAGATGATTACTGGC[C/T]TTTAATAGTAAGCTA | 56916 |
rs558577584 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288697 | TTTGCTACATTTCAG[C/T]CACATCTAATTTATA | 56916 |
rs558621916 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235455 | GAACCATAGGTGGTC[C/T]TGTGCCTGCCAGTTT | 56916 |
rs558649452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211827 | ATTAAATCTCAGTAA[A/G]ATGTCACCTTTTTAA | 56916 |
rs558690907 | in-del | -/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250344 | GTTCAGATAGTACAT[-/C]TACTAAATTCTGATG | 56916 |
rs558694547 | snp | A/G | | | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207233 | TCACTAATTACCTAT[A/G]CATTTGCAGGTCTCA | 56916 |
rs558707519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280467 | TTTTCCTTGATAAGT[C/T]TGTTACACTAAAAGG | 56916 |
rs558748441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244651 | AACGTCAGCCTTTGA[A/G]GTTCATGTCAGGTAT | 56916 |
rs558752166 | snp | C/T | | | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252939 | GAACTTACTTTGATT[C/T]CTCAGTGTTCTCAGA | 56916 |
rs558755596 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286785 | GTTATGTTCACCTAC[A/G]TTGTCTGTTAAAATA | 56916 |
rs558769306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273404 | CAATGAAGATCTATC[C/T]ACTGCTCAGTAAAGT | 56916 |
rs558791293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274442 | GTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 56916 |
rs558811131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259673 | TTCATTGCCTCCCCC[A/G]TTTTGTTATTACAAG | 56916 |
rs558832822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272867 | GCTGGAGTGCAGCGG[C/T]GCACTCTCAGCTCAC | 56916 |
rs558844968 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237758 | CTGTGACTACCCACA[C/G]GATTAGTTTAACTGT | 56916 |
rs558909789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225853 | ACAAAGTAAAAGTAC[A/G]AGAGGAAAGTATTAG | 56916 |
rs558957981 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213221 | CAAAATACTAAGCAA[A/G]GTAGAATCACTATCT | 56916 |
rs558969892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225385 | TCTTATAAGGACATC[A/G]GTCATATTGGACTCA | 56916 |
rs558988076 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220176 | AATCTAAGTGTTCAG[A/C]ACTATTCTAATTCTG | 56916 |
rs558994666 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277875 | AGCAGATTTTATGAA[-/C]CATTTTCTATCTTCA | 56916 |
rs559024349 | snp | A/G | 8.2588e-05 | 0.00642551 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226275 | AAGAGAAAACATTCA[A/G]CAAAGATACAGTGAT | 56916 |
rs559026036 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219543 | GTACTGGATAAACTT[C/G]GGATATAAGATTGTC | 56916 |
rs559026066 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219882 | TATTTTGCTTTAATA[A/T]CCCCCACCTGGTACA | 56916 |
rs559132627 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219391 | CTAGTGATTTTTTTT[G/T]TTCGAATGAGCCTTA | 56916 |
rs559170251 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232010 | GGGATTACAGGCACC[C/T]GCCACCATGCCAAGC | 56916 |
rs559234113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238090 | TGTTCCCATGGACCC[A/G]TCATTCTCCAATAAT | 56916 |
rs559273715 | in-del | -/GGTGTAG | 0.00478085 | 0.0486577 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288637 | TTAGATTATAGCTGA[-/GGTGTAG]GGTGTATATTTGTGA | 56916 |
rs559296104 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290667 | GTTGTCTATTTGATA[C/T]TTAACTCTTTATTAA | 56916 |
rs559296900 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282717 | TTTTTTTTTTTTAAA[A/G]AAGAGAATCCACTTA | 56916 |
rs559312710 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287013 | GGGACTATAGGTGCC[C/T]GCCTCCATGCCCAGC | 56916 |
rs559346711 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212647 | GCACACCACCACAGC[C/T]GGCTAATTTTTGTAT | 56916 |
rs559370929 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276033 | CGATCTTCTGACCTC[A/G]TGATCCGCCCGCCTC | 56916 |
rs559372547 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268645 | AGCTCTGGATCACAC[C/G]TGGATTGGATACTGA | 56916 |
rs559400671 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231792 | CTGTGTTAATCTAGA[A/G]TGGGCCACTCCCCTT | 56916 |
rs559430756 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287014 | GGACTATAGGTGCCC[A/G]CCTCCATGCCCAGCT | 56916 |
rs559540046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245555 | GCAGACATAACACAA[A/G]GACAGTGAGCTACAA | 56916 |
rs559542154 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283453 | CCAGCAGTGTTGAAC[A/C]TCAACTGCACTACGT | 56916 |
rs559600287 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245043 | CCTGGAGTAATATAC[C/T]GAGAGTGTTTGTGTT | 56916 |
rs559648482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246212 | GCAACCTCCGCCTCC[C/T]GGGTTCAAGCAATTC | 56916 |
rs559678494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209126 | AACATTTTTAACCTC[A/G]TCAGCAGATTGTCAG | 56916 |
rs559685586 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268153 | TTTTATAACAAATAT[G/T]TCAATGTAATAAAAC | 56916 |
rs559723034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289362 | GACACTGAAGCAAAC[C/T]AGCCCTTGAAAGATG | 56916 |
rs559751178 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207759 | TGAGGGAAGAAAGAA[C/G]AAGCGAGCGATTGAA | 56916 |
rs559784265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288810 | AATCAACTCATCTCA[A/G]AATATTCTCAGTGCT | 56916 |
rs559805070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254822 | AAGTAAATACAGATA[C/T]GCTTTAAATTTTAAT | 56916 |
rs559814965 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291432 | GGAACTTACTACTTA[A/G]GATGTATTCTCATTG | 56916 |
rs559820492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94253447 | GGAGCTCCATGATTC[A/G]AAATGCCAGCCTAAG | 56916 |
rs559864672 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282139 | GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 56916 |
rs559875501 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213830 | TACCCATCCTATTTT[A/C]GTACCAAGGTAGTAG | 56916 |
rs559885724 | snp | A/G | 0.000166732 | 0.00912898 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252669 | AAAGAAGTTTCTTCA[A/G]GAAGTCAAAATTACC | 56916 |
rs559890497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270933 | AACTACTGCCACCTC[A/G]GTACCTTATATTTTA | 56916 |
rs559934618 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272873 | GTGCAGCGGCGCACT[C/G]TCAGCTCACTGCAGC | 56916 |
rs559953774 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270328 | AAGTAGCAAATTATG[G/T]TTGTGTTTTTTTGTC | 56916 |
rs560035745 | snp | A/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207114 | AATTAAAATATTTTT[A/T]AAAAATTAATTAATT | 56916 |
rs560077263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228006 | TCTGAGGAGGAGCAG[C/T]TATTGAGGTAAAAGG | 56916 |
rs560098041 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254774 | CAGCAAAGTAGGTGA[A/G]TGAGCTTTTTCAAAT | 56916 |
rs560116070 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208374 | AGCCCCCATCCCTGC[A/G]AGGTGGTGCTTTCTA | 56916 |
rs560213674 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215641 | GGGGGGTGGGGGGGA[A/G]GAGGGGGATAGAAAT | 56916 |
rs560262385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216594 | GAAACTGAAACTCTT[C/T]ATGCATTGAACAACT | 56916 |
rs560316826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247905 | TACAAACGTATATTG[C/T]GTGATGCTGAAGTTT | 56916 |
rs560351311 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291776 | AAATTTAAGGAATTC[A/G]GATTGTTTTAACTCT | 56916 |
rs560363200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262041 | CTAAATGTTGGTGTT[C/T]TTCAAGGTTTTGCTC | 56916 |
rs560447975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214922 | TTAAAACTATACCAG[C/T]CGTCAGAAAGATTTC | 56916 |
rs560484759 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272972 | GCCACCATGCCTGGC[G/T]AATTTTGTATTTTTG | 56916 |
rs560534821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265477 | TTTCCCCAATTTGCT[A/G]CTTTCAATAAAATAC | 56916 |
rs560568041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244300 | AACAGTGCTACAGTT[C/T]CCTACAAACAATGCT | 56916 |
rs560602112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256571 | TTTCACCATGTTGGC[C/T]AGGCTGGGCTGGAAC | 56916 |
rs560619328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242718 | AGACCAGCCTGAGCA[A/G]TATAGTGGGACTCCT | 56916 |
rs560631584 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235736 | TCTAATAGAATAAAC[A/T]TGGAGTATTAAAATA | 56916 |
rs560682169 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223717 | GAACTACTGGCGTGC[A/C]CCACCACTCCCGGCT | 56916 |
rs560734888 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234788 | CCTTTGTATTTTCAC[A/C]TTTGTATCTGTCTTC | 56916 |
rs560772343 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246498 | TATCTTGCCTCCAGT[A/G]TGCAGTGAGCTCCCA | 56916 |
rs560792376 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224464 | ACCCAGCTGATCTGT[A/C]TTTCACATACACCAA | 56916 |
rs560829466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231050 | TGTCCTTAGTGAGAA[C/T]AGTTTCACTGAGTTG | 56916 |
rs560840457 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94253828 | TTTGCTTCAACCCTT[A/G]CGTGGGCTTTTATAG | 56916 |
rs560877939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243828 | TTTGTGATCTTTTCT[A/G]TTTGAAAAAAGCACT | 56916 |
rs560903419 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228211 | CCTGCATGGTTAATC[A/C]TGAGGAAAATTGTCA | 56916 |
rs560931669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257104 | CTTTGAGTAGTCACT[C/T]GAGTTTTTAATGAAG | 56916 |
rs560948406 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210602 | GAGAGGTTTCAAAGT[A/C]ATGAAGGGCAGGGTT | 56916 |
rs560951621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259766 | CCTTCCATCATATTA[C/T]TTTGAAGCACATCTC | 56916 |
rs561044362 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287828 | GACTACATACTTTTT[C/G/T]AATTTTTTTATTACA | 56916 |
rs561118470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245161 | ATATTGATCTAAGAA[A/G]AACAGTTTGGACTCG | 56916 |
rs561130589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94251028 | GCCTGTTCTTTATCA[C/T]AGTGTAAAACAAAAC | 56916 |
rs561135541 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287763 | TAATTGTATTAATAC[A/C]TTTTTTACCTTTTGG | 56916 |
rs561213288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258938 | AAGTTCTAGCCATAT[C/T]GAATCAAACTTTCTA | 56916 |
rs561247545 | snp | A/C | | | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94251832 | GGCTTTTTGATAATA[A/C]TGTATTTGAATAATT | 56916 |
rs561402529 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214343 | TCTCAACTCACTGCA[A/G]TCTCTGCTCTCGGGT | 56916 |
rs561406770 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207347 | TGCTATCTACATTAT[A/G]TTATAGGTGAAACAC | 56916 |
rs561447822 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244570 | GGCACCAGTGCCAAA[A/T]GGAGATTTGAAGCTG | 56916 |
rs561464654 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245613 | CATTCATTTTCAGAT[A/T]ACCTGTTTTTTGCCA | 56916 |
rs561492227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213902 | AACTTGGGACTCATC[A/G]ATGTCCTAAGCAGGG | 56916 |
rs561510738 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227062 | CTCAATTGAGAAGAC[A/G]GTGCTTAATTGAGAA | 56916 |
rs561528124 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212446 | TCTGAAAGTGCTAGG[A/T]TTATAGGCATGAGCC | 56916 |
rs561582937 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288530 | TCCCTAAGAGTTGAT[C/G]TACTATTTTGTGTTC | 56916 |
rs561589119 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226580 | TTATTATGGAAGTTT[A/G]AAAGAATTGTTTAGT | 56916 |
rs561652745 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269913 | CCTGAGCTCAAGCAA[G/T]CTGCCCAGCACAGCC | 56916 |
rs561706007 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220237 | TATAAACGGCTTTTA[C/T]TGATTTTATTTATTA | 56916 |
rs561737817 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261214 | TTTGAATATATCCAC[G/T]TAGTATAATCTAACA | 56916 |
rs561775821 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215241 | GAAAAGCAATACTTA[A/G]TTAAAGGGTTAGTGC | 56916 |
rs561817180 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223322 | ATATGGTGAAACTCC[A/G]TCTCTACTAAAAATA | 56916 |
rs561819132 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239485 | AAAAATGTATATCCA[A/C]AGTTTTTACTCTACT | 56916 |
rs561838052 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217416 | TATAGTGTCATATAT[A/G]TGATGTATCCTAGAT | 56916 |
rs561842163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225908 | TTTTGCAGTTTCCAC[C/T]AAAGTCTTGTTAGTA | 56916 |
rs561854487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234573 | CACTCTTGCTGAGAA[A/G]TATTGATTTAACTAC | 56916 |
rs561970372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232686 | GGCTAGGCATGGTGG[C/T]TCACACCTGTTATCC | 56916 |
rs561977302 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276049 | TGATCCGCCCGCCTC[A/G]GCCTCCAAAAGTGCT | 56916 |
rs561988857 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226355 | TTTTCCAAGAAAAAA[A/G]CCTACCTAATTTGAG | 56916 |
rs562010025 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228466 | AGAAATACCAATTAA[C/G]ACTAGTACAGTACTA | 56916 |
rs562040118 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282053 | TCAAAAAATAAATAA[C/T]TTTCTTTTAAATTTT | 56916 |
rs562084619 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268011 | ATTGCATTTTCTTTG[A/G]TCCTTTTACATGCTG | 56916 |
rs562110940 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291453 | ATTCTCATTGGTTCC[A/T]TCATTGGACTGATGT | 56916 |
rs562145605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241732 | GCTATAATGGGAACT[C/T]GTTGGCCTCTGTTCC | 56916 |
rs562182389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221583 | AGGTAGAAACAGATA[C/T]GAGAATCCAGCCATC | 56916 |
rs562187267 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283974 | AGGAAGTAAATTGAG[C/T]TGTAAATTATTTTAG | 56916 |
rs562252318 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290417 | CAAAATGTTGGTGAC[A/G]TTTTTCTAGCCTGGC | 56916 |
rs562315599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94253628 | AGAAAAATTTCTGGA[A/G]GCCTATAATTCAAGC | 56916 |
rs562324508 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94263327 | TAGCTAAAAGTTCTA[A/T]TAGAACCTCCTTAAG | 56916 |
rs562340784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248786 | GAAATTTTATTTTAC[C/T]CCATTGTGCAGAGGA | 56916 |
rs562364307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282932 | TTGGTAGGGGTAGCA[A/G]TATCGTAGAAAAGAA | 56916 |
rs562366146 | snp | A/C/T | 0.000489197 | 0.015632 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290587 | CCAGTACAGGACCGC[A/C/T]TGAAGAGAGAGCCAT | 56916 |
rs562384272 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279561 | TGACTATTTTTATAA[A/G]TAAGGTTTTACTATA | 56916 |
rs562386857 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262210 | CCACTGGCTCTTTCT[C/T]GAAAATTTGGTAGCT | 56916 |
rs562411337 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255538 | CAAGGTAGTAGACAT[A/G]TAAATGTAATATAAG | 56916 |
rs562453025 | in-del | -/AAATA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222973 | TGTCTCAAAAAAAAT[-/AAATA]AAATAAAAATTGTTA | 56916 |
rs562513387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248133 | CATTAGCTTGCTTAG[A/G]AAATGGTTTCCAGCT | 56916 |
rs562589652 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271765 | GGTTTGGGGTCCCCA[C/G]CTTTGCCTTTCAGGA | 56916 |
rs562603082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211431 | TTTAAGGTCAGGACT[A/G]GAGATGAAAATTGGT | 56916 |
rs562647892 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256393 | TTGAGACAGAGTTTC[A/G]CTCTTGTCACTTAGG | 56916 |
rs562732659 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209165 | GTATTTGAGGATAAG[C/G]CAAAAATTAAGATTT | 56916 |
rs562817223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215840 | TTTTTTAGTTTAAGT[A/G]TGTTTTCATAAATTT | 56916 |
rs562861567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273982 | GTTTCATAATACTTT[C/T]AGTTACTTTTAAAAG | 56916 |
rs562862605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279331 | TTTTTGTACGGATGG[A/G]GTTTTGCCATGTTGC | 56916 |
rs562882920 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224303 | TTGGTGCTCTCTAGA[C/G]CAAATAGTAGTTGTA | 56916 |
rs562939215 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257990 | ATGACTATGCAAATG[A/C]CTTTCATAGATGAAC | 56916 |
rs562997893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273116 | CAACCTATTTAGGTT[A/G]TTTCCAGTGTTTGGC | 56916 |
rs563008019 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223725 | GGCGTGCACCACCAC[C/T]CCCGGCTAATTTTTT | 56916 |
rs563028148 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236399 | TGCATATGTTCTTGA[A/C]AAGATTCAGACAATT | 56916 |
rs563113247 | in-del | -/CT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268321 | TGACAGTTAAATAGA[-/CT]CTTTTCCCAATGTGT | 56916 |
rs563118135 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243504 | ATTTGATGTTCTGTG[G/T]TCAACCATTCTGCTT | 56916 |
rs563177027 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242144 | GTTCAAGCAATTCTC[G/T]CACCTCAGCCTCCGG | 56916 |
rs563181209 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230197 | CTACAAAGGATATAC[C/T]CAGATCCCTTACTCT | 56916 |
rs563194548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267610 | AAATCATAGTAACTC[C/T]GGAGGGAATTTTTTT | 56916 |
rs563260570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274800 | CTCTGTTACTATGGT[A/G]AGAATATGTCATTCT | 56916 |
rs563304673 | snp | A/C | 8.25921e-05 | 0.00642567 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94280621 | TGAGGCTAACCCTGA[A/C]CTGATCTTTGAAGAT | 56916 |
rs563316702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237927 | ACATTTTAAATTTTA[A/G]TATGTATTTCCATGT | 56916 |
rs563334362 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244343 | GCCTTTGGCTGTCAG[A/T]CATAACTATTAGTGT | 56916 |
rs563353193 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275542 | TTTAAAAATTCATGC[A/G]GAATTTTATTTTTTC | 56916 |
rs563481478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250210 | AAAAAAAAAGACTCA[C/T]GCCACGCATCCTGTT | 56916 |
rs563519853 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224291 | AATGTTTGTGTTTTG[A/G]TGCTCTCTAGAGCAA | 56916 |
rs563527551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259846 | CATAACATTCTTATA[C/T]CTAATAAAAATCATC | 56916 |
rs563541691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245643 | ACTTTACAATAACTC[A/G]TAAGCTGTAACTCTT | 56916 |
rs563570889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286950 | GCGCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC | 56916 |
rs563582994 | snp | A/T | 0.0829062 | 0.185956 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242758 | AAAAAAAAAAAAAAA[A/T]TTTTTTTAATTAGCT | 56916 |
rs563784025 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213724 | GATAACTCAAATGTT[C/T]CTTGCTTGGACAGCT | 56916 |
rs563816832 | snp | C/G/T | 5.21683e-05 | 0.00510704 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233935 | AAAATGTTTTTTGCT[C/G/T]CTCTAAAAATATTTT | 56916 |
rs563841947 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277351 | AAAATAGCAATTTCC[C/G]TAATCAATGGCCAGA | 56916 |
rs563876653 | snp | C/G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207896 | GGATGCCCGCCAGCA[C/G/T]GGCCTCCGCCGCTCC | 56916 |
rs563884082 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219465 | GACCACCGAAAAGGT[A/T]AAACCAGTGGCAAGC | 56916 |
rs563911552 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261984 | TTGGCTTCTCTGATA[C/G]CACATCCTACATTTC | 56916 |
rs563923354 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206379 | ATATTAAAGGAAATA[A/G]GGCAGGCACAGAAAA | 56916 |
rs563971885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282789 | TCTGCCAGTAGGAGC[C/T]GATATACTTCTGAGA | 56916 |
rs564028025 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234351 | TAAAGCCTTAATAGC[A/G]AACATAGGTTGTGAG | 56916 |
rs564044273 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268848 | AATATGGTAAATATT[A/C]CAGTTTTAGCATTTA | 56916 |
rs564056273 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94253649 | TAATTCAAGCGTTAG[A/G]TGAAGGGAAGGCATA | 56916 |
rs564059892 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276581 | ATGTAGTTTAATATA[G/T]GTAGTATTCTGTGTT | 56916 |
rs564147166 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240095 | TGTATGTATGTATTT[G/T]AGCTGCATAGTTAGG | 56916 |
rs564156617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261311 | TTATCTGTTTCTCAG[A/G]AAATATTGACTGTTA | 56916 |
rs564206057 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222968 | GACTCTGTCTCAAAA[A/G]AAATAAATAAAATAA | 56916 |
rs564244248 | in-del | -/AAAG | 0.0509478 | 0.151255 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238613 | CAAGACCCTGTCTCA[-/AAAG]AAAGAAAGAAAGAAA | 56916 |
rs564264179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233098 | GTACATATAGAGAAA[C/T]TGCATATTCTAGATA | 56916 |
rs564300923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232740 | GGCGGATCGCTTGAG[C/T]CTAGGAGTTCAAGAC | 56916 |
rs564304302 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261605 | CATTATAATTGGTGA[A/G]AGATTAAGTTTGTTT | 56916 |
rs564365207 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270060 | AAATAAGGTTTTTGA[C/G]ACTTGAATGCTACTT | 56916 |
rs564376181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227116 | AAGGGGGTGAGAAAG[C/T]GAACCATGTAGATGT | 56916 |
rs564483869 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271846 | TGTAGATAGTCTTTA[A/T]ATCATAAGATTGCAT | 56916 |
rs564539237 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272298 | TGTCAGTGGGAAGGA[C/G]GTGGACACAATTCAG | 56916 |
rs564549326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249470 | AGTGATCTTAAGTCA[A/G]CAATATTTTTCATCC | 56916 |
rs564591742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279442 | ACTGCACTGAAACAC[A/G]AAAAACACATTTTAG | 56916 |
rs564644232 | snp | G/T | 0.00014794 | 0.00859931 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289781 | TCATTTTACAAAGCA[G/T]TTTTCTGAATGGGGA | 56916 |
rs564646041 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291373 | ATATTGGGCACAAAT[A/G]AGATTATCTTATGTG | 56916 |
rs564661792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241994 | CATTCACACAAACAC[C/T]GTTATCCTTCTATTC | 56916 |
rs564702300 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241660 | TCTTTCATGATGAAT[C/T]GTGAAGGTGTAATCA | 56916 |
rs564764164 | snp | A/G | | | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208675 | TTTATTCTTGATGTC[A/G]TATATATTGATGCAT | 56916 |
rs564785513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283601 | GAGACTGAGGCGGGC[A/G]GATCATGAGTTCAGG | 56916 |
rs564805404 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216550 | ATACATTGTCATGCA[A/G]CTATTCTCCAGCACT | 56916 |
rs564816216 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233897 | CATAGACACTATAAT[G/T]AAATAACATTAGTAA | 56916 |
rs564829942 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280488 | CACTAAAAGGTTCTA[-/T]GATTTAGATATTTTA | 56916 |
rs564844246 | snp | C/T | 0.000148447 | 0.00861404 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285078 | GATGAAGGTGAGTTG[C/T]TTGTAAGCAGAAACT | 56916 |
rs564867457 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236440 | GTAAAAATTAAGAGC[A/C]CCTATCCCATTTATC | 56916 |
rs564906475 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216455 | TGTTAATTTTAAAAA[C/T]TATGATAAAATACAC | 56916 |
rs564907612 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242969 | ATCAGGTCATAAAGA[A/C]TTTTCTCTTTTCTTT | 56916 |
rs564949070 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285908 | AGGAAATACAGTAAA[C/G]TGAATGCATAAGGCA | 56916 |
rs565076233 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94209875 | TATATTTGTCTGTTT[C/T]CTCTGTAGTTAGATA | 56916 |
rs565122654 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226503 | TGTTTTCTGGATAAC[-/AG]TGATTTTTTTTTTTT | 56916 |
rs565143783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210534 | GAAAACATTTAGGCA[A/G]CTCCTGTAATTGAGC | 56916 |
rs565158514 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257023 | AAATATCTGTACAGT[A/G]AGAGTGACACACTGT | 56916 |
rs565181313 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256660 | GAGCCACTGCATCTG[G/T]TCCTTTGCTTTGTTT | 56916 |
rs565182610 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273185 | TTTGCCAACATAAGC[G/T]CTCATATCTCATGAT | 56916 |
rs565254493 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247048 | TTGTATAGGTCAAGG[A/T]GGCATCTTACATTGG | 56916 |
rs565271351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258667 | TGATAGATGAATAAC[A/G]TAGTGAAGCTAGATG | 56916 |
rs565285199 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267391 | GGGACATAAACTTTT[G/T]GTCGGACAGCATCCG | 56916 |
rs565317988 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270269 | ACTGATATTAGGAGT[A/G]ATTGACACACATTCA | 56916 |
rs565395325 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282412 | AAATACGTTTTGAAA[C/T]AGCTATTAGAATTGT | 56916 |
rs565404574 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218000 | TCAGTCAAAAATGTT[G/T]GAAAAACACTGTTCT | 56916 |
rs565406123 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250952 | GGTGGGATTGCAAAA[G/T]ATGTTGAAAGTAATG | 56916 |
rs565406701 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266765 | CAAGTTCTTCATGAC[A/G]AAGTTTACTTTGCTA | 56916 |
rs565464525 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230962 | GTTTGTCAACAATGT[A/G]CAGGACAACACAGGA | 56916 |
rs565497179 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235823 | TAATGTAGTTCAGAG[-/T]TTTTTTTCTTGTAAA | 56916 |
rs565498649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237301 | ATTGTGGTTTTATTA[C/T]AGGTTTACGAATCTT | 56916 |
rs565503843 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230291 | TTCGTGTATTTTTTT[G/T]TTTGTTTCTTACACA | 56916 |
rs565525500 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211864 | CTTCCTTGATCACCC[G/T]GTGAAATAGCCACCC | 56916 |
rs565538551 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238841 | AATTCATCTTATTCA[A/G]CTTATTCATTAATTT | 56916 |
rs565581521 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258398 | GACCTCAAGTGATCC[C/G]CTCACCTCCACCTCC | 56916 |
rs565610998 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218409 | GACCTCCTCCTGACT[C/G]AGCCTCCTGAGTAGC | 56916 |
rs565649496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224646 | TATTTACAGATACAG[C/T]TCGTGAGCCCTAATA | 56916 |
rs565652227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259162 | TGGAAAGTGTTGTTT[C/T]TTCCTGCCGGTAGAA | 56916 |
rs565718137 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267678 | TGCCTCATTTTCTTT[C/T]ATTATCTCAGAAAAT | 56916 |
rs565742594 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286309 | GTTCCTCAGACTCAT[A/G]TTCTCCAAAGAGAAT | 56916 |
rs565764268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275898 | TGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT | 56916 |
rs565771616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230636 | CATTTCCCTAGTCAA[A/G]ACAATCAGAAATATC | 56916 |
rs565815043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212591 | TCCTGGGTTCAAGCA[A/G]TTCTCCTGCCTCAGC | 56916 |
rs565910552 | snp | A/G | | | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206019 | GGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCAT | 56916 |
rs565919038 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282707 | AAAAGTAATGTTTTT[C/T]TTTTTTAAAGAAGAG | 56916 |
rs565938019 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232860 | TGGCAAGCACCTGTG[G/T]TCTCAGCTACTCAGG | 56916 |
rs565964826 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282317 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG | 56916 |
rs566050049 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249793 | TTAATCAGTGTGTAC[A/T]AAGTGTTTTTATTAT | 56916 |
rs566050798 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226846 | AGGAATAGGGAGTTA[A/G]GGTCAGGGAATCGTT | 56916 |
rs566099256 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232537 | ATGCAAAGGAAATGC[A/G]TGTGATTGTCCTCAA | 56916 |
rs566104872 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289735 | TTCAAAAAAGAAGCC[A/T]CAAATATGTAGTTCT | 56916 |
rs566116881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287377 | TATAAACAAAAATGT[A/G]TATTTGTAATTGACT | 56916 |
rs566143398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252150 | CCACCATGCCCAGCC[C/T]ATTTGAATAATTTTT | 56916 |
rs566231404 | in-del | -/G | 0.00478085 | 0.0486577 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256777 | CCAGTGAATTTATTT[-/G]TAAGATTACTATATA | 56916 |
rs566443875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283681 | ATACAAAAAATTAGC[C/T]GGGCATGGTGGCGGG | 56916 |
rs566478759 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246920 | GTACTTGATTGATAA[C/G]TGCATAGCCATATTG | 56916 |
rs566560379 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276805 | GAGGACACAAGTTAC[A/C]TACTTATAAAAGAAG | 56916 |
rs566582551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233475 | ATGTTTTGTTTCTGG[C/T]AGAGATTCCTATATT | 56916 |
rs566623225 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94253801 | TACAGATAAATATAA[G/T]AACTCTTAAATTTTG | 56916 |
rs566643737 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273842 | GAGATGAATATTAAT[C/T]TTATGGTCTCTTTAT | 56916 |
rs566645878 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214243 | ATATGTTTCAGGATT[A/C]TTGAAAATTGAGCGT | 56916 |
rs566700606 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260852 | TAATTAATTTATGCT[C/G]TCAAAAAATAAGTAA | 56916 |
rs566767405 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208674 | TTTATTCTTGATGTC[-/AT]ATATATATTGATGCA | 56916 |
rs566804007 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207563 | CTCGACATTGTCGGC[C/T]CGCGCGTTGTTTGGG | 56916 |
rs566820867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248290 | TATGACTTAGTGATA[C/T]TCCATTTTATGTGTT | 56916 |
rs566831706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221819 | CATTTTATTAGGTCT[A/G]TATGTACATGGAGAT | 56916 |
rs566897069 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209289 | TCTGTCATTTAATTT[G/T]CACAATAATCCTACA | 56916 |
rs566912120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94263782 | CTAATAGATGGTTTT[A/G]TTTTAGTTTCCTAGA | 56916 |
rs566936030 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213159 | GAGAAAATGGTATGT[A/T]AATATATAGTTAAAA | 56916 |
rs566947492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228307 | GAATTACCCTTGTTA[A/G]CATTTTCCCACAATT | 56916 |
rs566960118 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272645 | TAATGTTATTGAGAT[C/G]TATCTGTGTTCTTAT | 56916 |
rs566983870 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265868 | TTTCTGATAGGTTAA[A/G]ATTAGCAGTAGGATC | 56916 |
rs566987542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234218 | ATTTTTCTAAAGATA[C/T]CTTACGTTTGAAGAT | 56916 |
rs566989524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277287 | TTTAAGTAGGTGATA[A/G]CTCTATATTTGGATT | 56916 |
rs567044673 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273283 | TTGCCCTTAAACCAT[C/T]CAGTGGATATTAAAC | 56916 |
rs567045092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265054 | GCACATAAGTGGACT[A/G]TGAACTGTTTTTCAT | 56916 |
rs567113604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218054 | TTGCTTTATTAAGAG[C/T]ATAGAGAAAAGTTAA | 56916 |
rs567118246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243051 | GAAACCTCTGCCTCC[C/T]GGGTTCAAGTGATTC | 56916 |
rs567194057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271271 | AACAAATCCACATAT[A/G]TATCAGCAACATCAT | 56916 |
rs567338748 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217500 | AGCCATTTTTATGAG[C/G]TTTTGTCTCTTTTTA | 56916 |
rs567398938 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249182 | AGTTTTATGTTGTGA[C/G]TGAACAATTAATATT | 56916 |
rs567426328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284259 | GTGAAGCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 56916 |
rs567448241 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225355 | CTTCTTTTGCATCCC[A/G]GTGTGTCTCCCTTTT | 56916 |
rs567452473 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280318 | ACCCTTGTTTCATCT[A/G]TACCCCAGACTTCTC | 56916 |
rs567458524 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284615 | TTTTAAGTGGAGACA[A/G]GGTTTTGTCATGTTG | 56916 |
rs567458652 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249036 | TGGACTTTAACCAGT[A/T]TCTTCAAGTGAAGTT | 56916 |
rs567485141 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254616 | GCATTACTTACTTAA[A/G]CCTCCTAACATCTTG | 56916 |
rs567503247 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223451 | TGAGCTGAGATCACG[C/T]CACTGTACTCTAGCC | 56916 |
rs567552265 | snp | G/T | | | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209459 | AAGGAATGTTGGAAG[G/T]TATATTTTAATATTT | 56916 |
rs567648639 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274138 | GTACATGTGAATGTA[A/T]CAAAGAAAACCCCCT | 56916 |
rs567662696 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280248 | TAGAATTGCATAATG[A/G]AACTGCCCATATGTT | 56916 |
rs567701096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213338 | CAATGAAATCATTGT[C/T]TACTGGGTGAACAAA | 56916 |
rs567742895 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249897 | TTTATCAATGTTATA[A/C]AGTATTTTCATACTG | 56916 |
rs567747883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280923 | TGAACATTTTCTTGA[C/T]GTATTTTCTTGATTA | 56916 |
rs567773764 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277643 | CTCTTCACAAGAAAA[A/G]TTTTGTTACTTCTTT | 56916 |
rs567790698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238209 | ACCTTTAATTTCCTC[C/T]AGTTTGAGCAAGGAG | 56916 |
rs567808410 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257565 | CATCTTTCCTTAAGT[A/G]AGAGCCCCTCTTTCC | 56916 |
rs567832203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258217 | TGGAGTGCAGTGATG[C/T]GATCTCAGCTCACTG | 56916 |
rs567841764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210886 | TTGCAGTGAGCCTAG[A/G]TCACACCACTGCACT | 56916 |
rs567920034 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250306 | GTACATTTACACTTG[A/C]ACTGATTTATTTGAG | 56916 |
rs567928574 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244021 | CATTATGGACCATCA[A/G]AGATAATGCCACAAA | 56916 |
rs568003969 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211685 | ACCCTCCTTCAGTTA[C/G]TGTGCCACCACCACA | 56916 |
rs568008553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94251685 | GCTTTCTGAGTAAGT[A/G]AAAATTTCTGAATAA | 56916 |
rs568037352 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266799 | ACTGTTGCAAATTTA[G/T]GTGAATTGTAGGAGA | 56916 |
rs568077849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213520 | TCCTGTGTCAGGGAC[A/G]GTAGATCTTATTTGG | 56916 |
rs568104686 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94263691 | TGATTACTTAGAGTT[G/T]TTAATGTGATTCTTG | 56916 |
rs568107363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260090 | TGGGTCATTTGTTCT[A/G]TAACTCTCCTGTCTA | 56916 |
rs568143763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288105 | TTTTTTCCCATTGAT[C/T]CATAATAAAGTCAAT | 56916 |
rs568148652 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221164 | CATGACTGTGAGTTT[C/G]ACAGCTTCCAGATAC | 56916 |
rs568148998 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218280 | TTTTAATTAATTAAT[G/T]GTTTTATTTTATTTT | 56916 |
rs568196024 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206599 | ATTTGATAGCACAAT[A/G]GCATGACTACAGTCA | 56916 |
rs568236411 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219666 | GTAAGTTCCCATTAC[C/G]TTTGGTAATAAGAAA | 56916 |
rs568240324 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225166 | ATACCAATCATACTA[G/T]TTTTCTAGAACTGCC | 56916 |
rs568270240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232564 | TCAAATATTTGAAGG[A/G]CAGGCATAGTGATAA | 56916 |
rs568277024 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231821 | TTTTCTGCTTCTCTA[A/G]AGAGATCAAGTCTTT | 56916 |
rs568318726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259303 | CATGAGAGATTAATA[A/G]CTTTATTTAAACCTG | 56916 |
rs568320266 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269361 | GAATGGGAGGCATGG[-/C]CTTGTCCTATGTTTT | 56916 |
rs568356518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227264 | TAAAGGATGAGATGA[A/G]GGAGGGGCTTCATCA | 56916 |
rs568465648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221051 | CAGATGTTTTCTCAA[A/G]ATGAACAAAGTAATA | 56916 |
rs568472752 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226876 | TTCTTTTTTTTTTTC[C/T]TGTTTTTTCTAGAGG | 56916 |
rs568472881 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269689 | TGTTGTTGTAATTGA[A/G]ACAGGGTCTGGCTCT | 56916 |
rs568481633 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270386 | TAAAAATCAAATCAA[C/G]ACAATTCAATTTTCT | 56916 |
rs568482298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283757 | GTGAACCTGGGAGGC[A/G]GAGCTTGCAGTGAGC | 56916 |
rs568491814 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245737 | GTGTGTAAAATTGTA[A/T]CATTTTTATTAGATT | 56916 |
rs568571301 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214264 | AATTGAGCGTTCTTT[C/T]GTTTTTTTTTTTTTT | 56916 |
rs568640391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288942 | TTTAATTAAAATATA[A/G]GGCAAACATTGGATA | 56916 |
rs568730798 | snp | A/G | 3.34362e-05 | 0.00408864 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276319 | TATAACCTTAGAGAT[A/G]TTTTTTCTTTTGGTG | 56916 |
rs568739008 | in-del | -/TGTT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236871 | TGTTTATATTTAATA[-/TGTT]TGTTCTTAAATATTT | 56916 |
rs568744870 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218785 | CATGATATGCAAATT[A/C]AGACTACAGATTTTA | 56916 |
rs568760043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254116 | TATTTGAAAAATACA[A/G]AAACAACATTAATAA | 56916 |
rs568766027 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270536 | AGAAATAGAATAGAG[-/A]ATAAAGTTTGAGAAG | 56916 |
rs568769547 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241767 | AGGTTGAGCACTGAC[C/T]GTAACAATAGCCAGA | 56916 |
rs568778850 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282358 | GCCTCGGCCTCCCAA[A/T]GTGCTGGGATTACAG | 56916 |
rs568792741 | snp | A/G | 0.000177478 | 0.00941847 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94290977 | TTAACCCCAGTCTTG[A/G]TGGTATATTGAACAG | 56916 |
rs568830484 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242174 | GAGTATCTGGGATTA[C/T]GGGAGTGCAGCACCA | 56916 |
rs568881611 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221338 | TAATACATGGTTAAC[A/G]GTTTTAACGTAATAG | 56916 |
rs568888661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210125 | ATCAGAAGATATTTT[C/T]CTGTTTTTATTTCTT | 56916 |
rs568892044 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284227 | AGCTACTCGGGAAGC[C/T]GAGGCAGGAGAATGA | 56916 |
rs568929431 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271368 | AAAGCTGAGTTCACA[A/G]AGTTTGTTATAGCCA | 56916 |
rs568941830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277442 | GATATATAGTATGTG[C/T]GGAAAGTTTGATCAT | 56916 |
rs569028110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247479 | TAAATATTTGATTCC[A/G]AAGAGCTGTTTACTG | 56916 |
rs569053193 | in-del | -/T | 0.486984 | 0.079614 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214428 | ACCACGCCGGGCTAA[-/T]TTTTTTTTTTTTGTA | 56916 |
rs569144540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249159 | TAAATTCCTTTTATC[A/G]TTGTTTCAGTTTTAT | 56916 |
rs569161288 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288824 | AAAATATTCTCAGTG[C/G]TAAATTGAATTAATC | 56916 |
rs569227130 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243248 | CCAACCTATCAGGTC[A/T]TAAAGAATTTTTTAT | 56916 |
rs569294194 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254529 | TCAGCAACTTAACAT[A/G]TGGAAAGCATATTTC | 56916 |
rs569308581 | snp | C/T | 0.000199154 | 0.00997683 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249642 | GTTTTCTTTTTTTTT[C/T]CTCCCCATTAGGGAG | 56916 |
rs569338389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231134 | AGAAAATCAGTCTAA[C/T]AAAATCTGTGAAATG | 56916 |
rs569345749 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222699 | TGGGCTTGGTGGCTC[A/C]CACCTGTAATCCCAA | 56916 |
rs569372124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258316 | TCTACCACCACACCC[A/G]GTTAATTTTTGTATT | 56916 |
rs569397451 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213663 | GAGTTGTAAATGATA[A/C]GCATTTGATGATATT | 56916 |
rs569438674 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250531 | GAGCATTAGAAATGC[-/A]AAAAAAATGTCAAGT | 56916 |
rs569534253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255893 | TAGCAGTAATGTAGG[C/T]GCCTATTGTGAGAAA | 56916 |
rs569543844 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215354 | CTGGGCACAGTGGCT[A/C]ATGCCTGTAGAGTCG | 56916 |
rs569543957 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217746 | AATAATAGATGAGTT[G/T]TATTATATCTTTGTT | 56916 |
rs569573940 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269665 | CTATTGTTTTCATTC[G/T]GTTGTTGTTGTTGTT | 56916 |
rs569631392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230446 | CTACATTGTGTGAAC[A/G]TTCCTTATTTTATTC | 56916 |
rs569665982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274021 | AGAAAATGAGTACTT[C/T]TAAATGTAGAATTAA | 56916 |
rs569691384 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255681 | TTTGTCAGATAATTA[G/T]GCTTTTTGAAACTAA | 56916 |
rs569738868 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218212 | GTCCCTCCTTTAGGT[G/T]TAACGCTTTTGCCTT | 56916 |
rs569745400 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232055 | TTTAGTGGAGATGGG[G/T]TTTCACCATGTTAGC | 56916 |
rs569746409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280951 | TTACCTCCTTTCCTC[C/T]GTTGAACCTCAGACA | 56916 |
rs569753390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266889 | TTATAGGGAAAAGCT[A/G]AAGTTTTCATATGTA | 56916 |
rs569806533 | in-del | -/CT | | | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209504 | TTTTTTTATGCAAAA[-/CT]CTGTTTCGTAAACAG | 56916 |
rs569834252 | snp | G/T | 4.94752e-05 | 0.00497344 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281424 | TGTCAAGGCTTTGAG[G/T]AGTAAAACGATTTTT | 56916 |
rs569960329 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279955 | CTGCACCCTCCGCCT[C/G]CCAGGTTCAAGTGAT | 56916 |
rs569962143 | in-del | -/TG | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267588 | ATTGAATTTTCAGAC[-/TG]TGGAGAAATCATAGT | 56916 |
rs569962830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259049 | GGCTTATGGGCACAT[C/T]ACCCACAATATATTA | 56916 |
rs569968687 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282994 | TAGCCAGAGGAGAAA[G/T]AACTGCAATACTAAG | 56916 |
rs569999736 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232124 | CACGTCGGCCTCCCA[C/G]AGTGCTGGGATTACA | 56916 |
rs570006299 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287238 | CGTCTCTTATTTACT[C/T]GTTTAGCTGTAATCA | 56916 |
rs570016993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231958 | CCTCTGCTTCCTGGG[A/G]TCAGATGATTCTCAT | 56916 |
rs570030812 | snp | C/T | | | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94205772 | CCCAAAGTGCTGGGA[C/T]AACAGACGTGAGCCA | 56916 |
rs570178222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232517 | TGAGAAGTCTAGGTA[C/T]AATAATGCAAAGGAA | 56916 |
rs570178502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225375 | GTCTCCCTTTTCTTA[C/T]AAGGACATCAGTCAT | 56916 |
rs570183352 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224191 | TGCTCAACTTGCATG[A/C]AATGTTTATAAAATT | 56916 |
rs570301176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245237 | CTGATGATCTAACCA[C/T]AGAAAACATTCAGCA | 56916 |
rs570382294 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206818 | TTTAGCAGAGACGGA[A/G]TTTCACCATGTTGGC | 56916 |
rs570448632 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246438 | CTGACAATCTTAAGA[A/G]GTATTTTATAAAATG | 56916 |
rs570472699 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266503 | ACCTATATGGATAGT[C/G]TCTTTAAAGTTTATT | 56916 |
rs570510105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94253133 | CCTGTGTAAAGTCAA[A/G]CATTACTTTCATTGT | 56916 |
rs570533768 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269499 | GCAAATTAAGTTTTT[G/T]TTTTTTTTTTATCTG | 56916 |
rs570554727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282402 | CGCCCGGCGCAAATA[C/T]GTTTTGAAACAGCTA | 56916 |
rs570569139 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239594 | ATTTTTTATTTTGAG[A/G]CAGGGCCTCACTCTG | 56916 |
rs570614308 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219849 | TTCAAAAGGGCAAGT[G/T]GAACTGTAACTTGCC | 56916 |
rs570614761 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260689 | GAGGAAGTATCTATA[A/G]AAGAACTTCTTACAT | 56916 |
rs570621255 | snp | G/T | | | intron-variant, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94213130 | AGTGAAGCCTGATCC[G/T]CCAAGAGCACCAGGA | 56916 |
rs570667201 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268827 | TAAGCCCATAGCATA[A/G]TCTGAAATATGGTAA | 56916 |
rs570724363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252308 | GGCATAGTTGAGTGG[A/G]GCTGCTAGGAATATC | 56916 |
rs570748626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232957 | TGCACACCAGTCTGG[A/G]TGACAGAGTGGAACC | 56916 |
rs570766353 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256412 | TTGTCACTTAGGCTG[G/T]AGTGCAATGGTATGA | 56916 |
rs570798686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271184 | GTATGTACATGTGTA[C/T]GTACATACATATATG | 56916 |
rs570807863 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207474 | AGATAATTTAACAGG[A/T]CAAAGGTACAGAACA | 56916 |
rs570825077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208642 | TTTAAAAGATGAAAG[A/G]CAGAAGGGATTCTCA | 56916 |
rs570858028 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215223 | TGTCTGTTAATGTTA[A/G]TTGAAAAGCAATACT | 56916 |
rs570862758 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261713 | CTCCCGGGCTCAAGC[C/T]ATCGTCCCACCTCAG | 56916 |
rs570907228 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233392 | TGAAGTTAAATAGAA[A/C]AGGAATAAAGTTAGT | 56916 |
rs570968327 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240688 | AAATAATGTGATGGT[G/T]TATGAATATAGTATT | 56916 |
rs571079971 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270411 | TTTTCTATTATAGAT[A/C]CTAGCTTAGTATTAA | 56916 |
rs571109606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247701 | CCCTCCTCCCCCTAA[C/T]CCCTGGCAACCGCCA | 56916 |
rs571110898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277253 | TTGTTTTCATAGTGC[A/G]TATGCTCTATGAAGT | 56916 |
rs571141517 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258655 | GTGCATACTAGGTGA[C/T]AGATGAATAACATAG | 56916 |
rs571165398 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283549 | AACAATTGACGGCCG[A/G]GCGCCGTGGCTCACG | 56916 |
rs571178586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276765 | TATTTATAAATAATC[C/T]TTCATCATCTCATAA | 56916 |
rs571339045 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283548 | TAACAATTGACGGCC[A/G]GGCGCCGTGGCTCAC | 56916 |
rs571393054 | snp | C/T | 0.000807591 | 0.0200784 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291033 | GCTAAAAGGAGTCTT[C/T]ATGTGTTAATACTAC | 56916 |
rs571409217 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241817 | TCTTACCTTGTTGAC[C/T]TGCATGCACAGACTC | 56916 |
rs571441947 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284199 | AGGCGTGGTGGCAGG[C/T]GCCTGTAGTCCCAGC | 56916 |
rs571451563 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239343 | AAATTGTGACAGTTC[C/T]CATTGTTTCTTTTAA | 56916 |
rs571475515 | in-del | -/CA | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236600 | ACAAACGTGAGCATG[-/CA]CACACAGGCACGGAG | 56916 |
rs571604879 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280862 | GCACACTGACTTGCT[A/T]GAATTAGCCTATGTC | 56916 |
rs571652043 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285533 | TTGGAAATAAGCAAG[G/T]TTTTTCATTCTAATT | 56916 |
rs571669751 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249851 | AAAAGCTTAGGGTGA[A/G]TTTTGTATTCTTCTA | 56916 |
rs571685945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244224 | GACCTAAAATAGAAG[C/T]CACTGTACCCTGCAT | 56916 |
rs571687918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250446 | TTGTAAAAGCCTAGC[C/T]GCATATTGAAATTTC | 56916 |
rs571705829 | in-del | -/TT | 0.00874735 | 0.0655527 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270898 | TTTAAAACATGAAAC[-/TT]TTTTTTGCTACTGTA | 56916 |
rs571723781 | snp | A/G | | | intron-variant, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94213054 | TTTGGAGGGATTGAA[A/G]TAATGGCAGGTGAAA | 56916 |
rs571723800 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247712 | CTAACCCCTGGCAAC[C/T]GCCAATCTGCCTTCA | 56916 |
rs571749566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249997 | AACCGTAATAAAAAT[C/T]GTGAACTCATTTATA | 56916 |
rs571757312 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279675 | GCCTACAAAGCCTAA[A/T]ATATGATCTGGCCCT | 56916 |
rs571782068 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230078 | ATTCATTTGAAATAC[C/T]ATTAATTATTTTGTA | 56916 |
rs571792982 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265717 | ATAAAACTGTTAATA[G/T]TATGATATTTATAGT | 56916 |
rs571874430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210750 | ACCAGCCTGGCCAAC[A/G]TAGTGAAACCCCGTC | 56916 |
rs571900276 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228932 | TCTAAATTTGGGTTT[A/G]ACTAATGTTTCTTCA | 56916 |
rs571911310 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217437 | TATCCTAGATTTTGA[C/T]GTGTTTTTGTTGTTG | 56916 |
rs571932861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249201 | ACAATTAATATTTAA[A/G]CCATTCTGTGAATCA | 56916 |
rs572013259 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237312 | ATTATAGGTTTACGA[A/T]TCTTAGTAGGAACAT | 56916 |
rs572060653 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230143 | TAAATTTTACTTTCA[A/G]ATATTTAAAATATGA | 56916 |
rs572069668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283831 | ACTCCATCTCAAAAC[A/G]AACAAACAAAAAAAT | 56916 |
rs572093561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286626 | CTTTCTCCTTTGTCT[A/G]ATTCCCTTACACTTT | 56916 |
rs572129480 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256612 | AGGTGATCCACCTGT[C/T]GCGGCCTCTCCAAGT | 56916 |
rs572259095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257805 | TATGTAATATAGTTA[C/T]AATGCACTTTTTGTC | 56916 |
rs572267037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257062 | AGTGATACTTCAGAT[A/G]CTGACTGTTTTTGAA | 56916 |
rs572277696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211231 | GAGCCGAGATTGTGC[C/T]ATTGCACTCCAGCCT | 56916 |
rs572320217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94266210 | CAGCATTGGATATGG[A/G]GAGTTCTTCACTCTA | 56916 |
rs572320636 | in-del | -/A | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94263326 | TTAGCTAAAAGTTCT[-/A]ATAGAACCTCCTTAA | 56916 |
rs572347889 | in-del | -/TGTTT | 0.0687284 | 0.172164 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280572 | TTTTGAAGTATACTG[-/TGTTT]TGTTTTGTTTTGTTT | 56916 |
rs572364617 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261397 | TCTTTAGATTTCTAC[C/T]GAATTGTGAATATGT | 56916 |
rs572403181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260307 | TACATGTCTGGATCC[A/G]TAATTCATTAGCCAT | 56916 |
rs572404071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267399 | AACTTTTGGTCGGAC[A/G]GCATCCGTAACCTGT | 56916 |
rs572406605 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282185 | GCTCACTGCAAGCTC[C/T]GCCTCCTGGGTTCAC | 56916 |
rs572416473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274500 | TTTTGTATTTTTAGT[A/G]GAGATGGGGTTTCAC | 56916 |
rs572457531 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94251960 | AGGTTCAAGCGATTC[G/T]CCTGCCTCAGCCTTC | 56916 |
rs572504646 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218697 | TTTAGTGTATTGTTT[G/T]TCTTTTCTAGGGTAT | 56916 |
rs572559691 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231537 | ATACCTTCCACCTAG[A/C]TTTAACAGTTGTTTT | 56916 |
rs572661839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281058 | ACAATCTGTATGTGT[A/G]CTTCAAAATTAGTTT | 56916 |
rs572671918 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232011 | GGATTACAGGCACCC[A/G]CCACCATGCCAAGCT | 56916 |
rs572708213 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233001 | AGAAAAAACACACAT[A/G]TTCTGTTCTTTGGAA | 56916 |
rs572759566 | in-del | -/AAAT | 0.00358779 | 0.0422022 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223495 | GAGACTCTGTCTCAA[-/AAAT]AAATAAATAAATAAC | 56916 |
rs572791240 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222829 | ATTAGCCGGGTGTCG[G/T]GGCAGGCACCTGTAA | 56916 |
rs572797291 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224909 | GAGAATTAATGACAG[C/T]TATCATTTTTAACCT | 56916 |
rs572806881 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246543 | GAGGCAGATAGGTGC[A/G]GCCTTTCTTTTTTCT | 56916 |
rs572811628 | in-del | -/ATTTGATTTTTG | 0.495818 | 0.0455352 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255737 | TTTTACATGAGGAAA[-/ATTTGATTTTTG]ATTTGATTTTTTTTA | 56916 |
rs572872542 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227017 | CTCGAGGGTCAGGGA[A/C]TGGTTTCTAAAGAGC | 56916 |
rs572881179 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239966 | GACTTAAAATATTAC[A/T]TTTAGAATATTGTGG | 56916 |
rs572883565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241308 | GCTTGCATATAATTT[A/G]TGACTGTTTTTGCTT | 56916 |
rs572893362 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289993 | TTTTATTATGTTAAA[G/T]AATGCAGCTGTATAG | 56916 |
rs572934157 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206891 | AGCCCCCCAAAGTGC[C/T]GGGATTACAGGCGTG | 56916 |
rs572946772 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247245 | CCAAATATGTCTGTT[C/G]CAACTATGATTCTGG | 56916 |
rs572969575 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241873 | AAATGGGCCTATTGA[C/G]CAGGCATTCAAGTGG | 56916 |
rs572972630 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269892 | TGCCCAGGCTGGTCG[C/G]GAACTCCTGAGCTCA | 56916 |
rs572995889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252383 | CCTTTGTTAGAAAAC[A/G]GAGATTTATATTTAA | 56916 |
rs573040788 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289141 | TTCCCTACTCCATTT[A/C]TTACATAAATGTTTT | 56916 |
rs573077289 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281964 | GGATTGTTTGAGCCC[C/T]GGGGGGCGGAGGTTG | 56916 |
rs573095367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221185 | TTCCAGATACTTAGA[C/T]ATTTCTGAGAAGATC | 56916 |
rs573132735 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220706 | GTGCAAAAGCAATCA[A/T]AGGTAAAATTGCTGG | 56916 |
rs573139986 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288405 | CTCCCTGCATTCTTC[A/C]TAACATAGTATCAGT | 56916 |
rs573142636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239415 | TAAACACTAGGGATG[C/T]TTTTATGCTGTTTGT | 56916 |
rs573145212 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240104 | GTATTTGAGCTGCAT[A/T]GTTAGGGCTCTGATA | 56916 |
rs573208580 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214560 | CATGAGCCACCGCAC[A/C]TGGCCAAGCGTTTGT | 56916 |
rs573268855 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233810 | GAAATGGAAAAAAAA[A/G]GTCTCTTTCTGACAA | 56916 |
rs573277863 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271277 | TCCACATATATATCA[A/G]CAACATCATTTCAGC | 56916 |
rs573332281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283473 | CTGCACTACGTAACC[C/T]TTCCATTTTCTAGTA | 56916 |
rs573401669 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276893 | ACTATATCATTTATC[A/T]CAGAATGTTAAATTA | 56916 |
rs573416422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254483 | TACAATTTTACCAGA[A/G]GTATATGTGCCAGAT | 56916 |
rs573417923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261171 | ACCTGTAATTGCTTT[A/G]TAAAGATTCAGTGTG | 56916 |
rs573432918 | snp | A/G | 0.000183672 | 0.00958134 | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208121 | TCAGTAAGGAGGGGC[A/G]GGCGGGGGAGGCGGA | 56916 |
rs573462715 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284558 | GTGTGCCACCACACC[C/T]AGCTAATTTTGGTTT | 56916 |
rs573485312 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268514 | GTGAATAGGATGACT[A/T]AAGAATTGGGAAGGA | 56916 |
rs573492991 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207790 | CGTTAAAAAGATGCC[G/T]TAGCATGCACTCCAC | 56916 |
rs573501577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94253498 | AAGAAGCAATTGTTT[A/G]TTTTCTTTTTTTCTT | 56916 |
rs573547738 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217601 | GTGACCAGAGAATGT[G/T]GTCTGTAGTATTTCT | 56916 |
rs573614926 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222820 | AATACAAAAATTAGC[C/T]GGGTGTCGGGGCAGG | 56916 |
rs573632816 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264625 | TAAATTAGCAAACTT[-/G]GTTTTCCTCATAAAG | 56916 |
rs573664972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94209739 | GGCTTTGTCTAAGTA[A/G]TTTTGAATTTAAATG | 56916 |
rs573675051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256174 | TTTTTATGCTGACCA[A/G]TGCGACATGCATCAG | 56916 |
rs573699639 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286901 | TCAGAGTCTTGCTCT[A/G]TCGCCCAGACTGGAG | 56916 |
rs573711882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228434 | CATTTGCATATTAAC[A/G]GTAATATTTCAAACC | 56916 |
rs573728302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277708 | CAGTTTTTTCAATAC[C/T]GCAGTGTTTACACTG | 56916 |
rs573752357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210306 | TAATCCTTGTAGGAA[C/T]GGAGCACTTTGCTTT | 56916 |
rs573831597 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236353 | GCAGTATAAAAACAG[C/T]ATATTAGAATGATGT | 56916 |
rs573874023 | snp | C/T | | | upstream-variant-2KB, splice-donor-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207529 | GACGGGTACGAATTA[C/T]CATGACAACAGCGCG | 56916 |
rs573899570 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228949 | CTAATGTTTCTTCAT[C/G]GTTAAATTTAGGTTA | 56916 |
rs573908048 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223720 | CTACTGGCGTGCACC[A/C]CCACTCCCGGCTAAT | 56916 |
rs573914633 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291784 | GGAATTCGGATTGTT[G/T]TAACTCTTACCAAAA | 56916 |
rs573949879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279709 | CAGGAACAGTTTGCT[A/G]ACTCCTAGTCTAGAC | 56916 |
rs573979574 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285699 | CGTATGATCAAATAA[G/T]TACTAGTCTTTCTTG | 56916 |
rs573992636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230076 | TTATTCATTTGAAAT[A/G]CCATTAATTATTTTG | 56916 |
rs574004347 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222088 | AAGGGCTATATATTT[A/G]CCCTGGTACGGAGAG | 56916 |
rs574029923 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243507 | TGATGTTCTGTGGTC[A/G]ACCATTCTGCTTTTA | 56916 |
rs574070899 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233789 | GATTTTTCACATAAC[A/T]ACACTGAAATGGAAA | 56916 |
rs574079660 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237837 | AGTAAATGTCCTTAT[A/C]CATAAATAGAACAAA | 56916 |
rs574089642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237093 | TTCTCATTAATATTG[C/T]TCCACAGTTTATCAA | 56916 |
rs574103325 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219646 | TTCCTGCATATGCTA[A/G]TAATGTAAGTTCCCA | 56916 |
rs574166127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238461 | TAGCAACTATTTGTT[C/T]AAGGGTCATCTGATG | 56916 |
rs574221125 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249277 | GTGGATATATAATAG[G/T]GAACATAGATGAGAT | 56916 |
rs574266466 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243458 | GGTAAATCAGATACC[A/C]AGATCACATAACGGC | 56916 |
rs574283832 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211395 | TGGATCTCTGGAGAG[C/G]ACAAGATACTGAAGT | 56916 |
rs574321915 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217913 | GCTCACATTTTCTTT[C/G]AGTTACACTTGCAAA | 56916 |
rs574336640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245363 | GATCAGATGTTTTAA[A/G]TGCTGTGAAAATAAT | 56916 |
rs574461204 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214186 | CATTCAGGAAAGGAA[A/G]GAGAGAAATAGGTAA | 56916 |
rs574529334 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260352 | TTTTTATTTTATTTT[A/T]TTTTATTTTGAGACA | 56916 |
rs574573000 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288623 | AAAGTACTCATAATT[A/T]TAGATTATAGCTGAG | 56916 |
rs574619218 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289093 | ATATAGATTGGTTTT[C/T]GTTGGTTTAGGTTTG | 56916 |
rs574632856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250576 | AGACTATTGTGTATT[C/T]GTGGAGGTGAAATTA | 56916 |
rs574667450 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250120 | AAGAATTTAAAAAGT[A/T]TTCCATTTCAGTGTC | 56916 |
rs574723544 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267185 | GTTCATCCTGAACTT[G/T]ACAGCATGGTTCCTA | 56916 |
rs574723604 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257835 | CATTTGTAGGTCTTA[G/T]CTATCAACTTAATAT | 56916 |
rs574733446 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232115 | TAATCCACCCACGTC[A/G]GCCTCCCAGAGTGCT | 56916 |
rs574769148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220043 | TCTTTTATGGTACTA[C/T]TTAAAAGTGCCTATT | 56916 |
rs574786998 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268945 | CCATTTGTTACTACT[A/T]TTATAGTAGTAGCAT | 56916 |
rs574799482 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268410 | GTGATAGGTTGTATG[C/T]TGGGATGGCATGTGG | 56916 |
rs574836168 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246081 | ACCTGGTACAGAGCC[A/G]TCTCTTAACCTGGGC | 56916 |
rs574901386 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252501 | TAACAATAAATTGTC[A/G]TTGAATTCTTCTGTA | 56916 |
rs574916386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212999 | TGTTATTTACACATT[A/G]TTTCTCCTTTTTTTC | 56916 |
rs574947905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275516 | CTGGCTTCTTGTGTA[C/G]GAGTCTGTCCTTTAA | 56916 |
rs574951185 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207628 | TACGCGCTCTTAAGG[G/T]TTCTCCGTGGTGTTT | 56916 |
rs575038822 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275958 | GCCCACCACCACACC[C/T]GGCTAATTTTTTATA | 56916 |
rs575064871 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289231 | GTGTATTTTTATATA[C/G]CTTTATAAAATTGGA | 56916 |
rs575087321 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267026 | TGTTTTATTCTTACT[A/G]TAGATGTAGCCATCT | 56916 |
rs575087683 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238347 | TTTCCTTAGCAGTAA[A/G]GTAGTATAATAGTGC | 56916 |
rs575101540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276866 | TAATAGCGGACGTCA[A/G]TTATTTAAATTACTA | 56916 |
rs575128481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220794 | TCTTAAAATTGTGTA[A/G]ATGCCAGTATCACTT | 56916 |
rs575176445 | snp | G/T | 2.01851e-05 | 0.00317681 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283107 | AGATTTAACCTAATT[G/T]GTTTATCTTACAGGA | 56916 |
rs575198815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234587 | AATATTGATTTAACT[A/G]CAGAAACAAAGGAGT | 56916 |
rs575224362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269948 | AAAGTGCTGGGATTA[C/T]GGGCATGAGCCACTG | 56916 |
rs575234806 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227091 | AAGACAGTGCTGGAG[A/C]AAAGACATAAAGGGG | 56916 |
rs575273063 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94263300 | TGGTTGCATTTAAAA[A/G]TAAAAGTATTTTAGC | 56916 |
rs575408388 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261891 | CTGGGATTATTGGTG[C/T]GAGCCACCACAACCG | 56916 |
rs575464194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214607 | GCTAGTGGAGAGGGA[A/G]GGACTGAGGGAGGGA | 56916 |
rs575494514 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240039 | ATAACATTCCATTTT[C/T]ATTTTGTAATAGCCA | 56916 |
rs575533730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208853 | GCATCCATAGGTCAG[A/G]ACGGTTGCTATTGGA | 56916 |
rs575558982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239517 | CAGAAGATAAGAGTA[C/T]GAATTTATTGATGTT | 56916 |
rs575587722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233080 | ACAACAGAAATAACA[C/T]GAGTACATATAGAGA | 56916 |
rs575660623 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291699 | CGTGTAGTGGAGAGA[C/T]GGGGTATGAGGAGAT | 56916 |
rs575675833 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283980 | TAAATTGAGTTGTAA[A/G]TTATTTTAGATGAAT | 56916 |
rs575693381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249916 | ATTTTCATACTGTTT[A/G]TTTATGTTGTTTATT | 56916 |
rs575697055 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277805 | ATTAACTGCCTTTTA[A/T]ACATTTACTAATTTG | 56916 |
rs575761974 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243691 | GAAATAGTAGGTGAT[C/G]ATAGAAAATTGCTTC | 56916 |
rs575779462 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211544 | CGTTAGTTTATTTAC[A/G]GTAAAGTGTCAGGTC | 56916 |
rs575801541 | snp | C/G | 1.66538e-05 | 0.00288559 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94278457 | CATATATGAAAAGGA[C/G]AGAATAGCACATGCA | 56916 |
rs575810678 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240495 | AAGACCTTGTGCAAG[G/T]CCTGGTACATAGTAG | 56916 |
rs575872958 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229055 | GTGTCAGGAGACACA[G/T]GATATCCATTTGTCC | 56916 |
rs575884987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256226 | ATATATGCATCTACT[C/T]TGTTAACATTTAGAT | 56916 |
rs575945048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262627 | AGACTTGTCTGTTGC[C/T]TCTCTAGGTTCTGAC | 56916 |
rs576014818 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216985 | AGTAATTCTATTTTT[A/G]ATTTTTTGCGGAACC | 56916 |
rs576017795 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243522 | AACCATTCTGCTTTT[A/T]TCAGGATTTATTGTC | 56916 |
rs576029827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255146 | GTTGAGGTTTTAATC[A/G]TATTGCTCAGTCATA | 56916 |
rs576101212 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210444 | GTGAATGGAAAATGG[G/T]GAAAGAAAGTTTTAA | 56916 |
rs576185773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272288 | ACGTATGTATTGTCA[A/G]TGGGAAGGAGGTGGA | 56916 |
rs576195517 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285766 | GAGGTGGGCGGTAGA[C/G]AAAGTTTGAGTAAGA | 56916 |
rs576211299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210985 | TCAAATAAGAATCGA[A/G]GGTCTGGCTGGGCAC | 56916 |
rs576219837 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248536 | TTTTGAAATGGTTTC[C/T]CCAGATGGGTTTCAC | 56916 |
rs576219895 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281738 | TAAGAGTAATTTCAA[C/T]GGTCAGGCATGGTGG | 56916 |
rs576240786 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265094 | CCACCCCCAAGTAGG[G/T]TATTTTATTCTATCA | 56916 |
rs576272829 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216420 | TAAATATACTCATTC[A/G]TATTTTCCTCTAGTA | 56916 |
rs576302332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272727 | GGTATGGTAGTCCGT[A/G]GTATAAATACAGTGC | 56916 |
rs576319254 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280403 | GTATGTTATCTCTCA[A/G]ACAGTAAGGACTTCT | 56916 |
rs576333136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279729 | CTAGTCTAGACTTCC[A/G]TAATGCACTTCTTTT | 56916 |
rs576390348 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266444 | GTTGTTGTTGTTGTT[G/T]TTTTAAGTGCTTGTT | 56916 |
rs576391419 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232215 | TCACTTGTATTTCCT[A/G]TAGTCTGGAAGATAA | 56916 |
rs576413273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268241 | TTTATTTAAATTTTA[A/G]AAATCTGTGTAGTTT | 56916 |
rs576414128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274416 | CCGCAACCTCCGCCT[C/T]CCAGGTTCTCGTGCC | 56916 |
rs576434878 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286650 | ACACTTTTTTCTCCC[A/G]TCGTATTTTAATGGT | 56916 |
rs576435017 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254059 | GTGGCAATAGGGGAG[A/C]GTCCCTGAACAATGG | 56916 |
rs576436986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216783 | TTTTTAAGACTGAAT[A/G]ATATTTCACTGTGTG | 56916 |
rs576454992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224865 | GTTTAAATGTTTATT[A/G]TATTTGAAGACTTGA | 56916 |
rs576499219 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267380 | GTCATACTTACGGGA[C/T]ATAAACTTTTGGTCG | 56916 |
rs576555860 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258605 | TGTTTCTGAATTCAG[A/T]GCATGCCACTTTTTT | 56916 |
rs576566726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237292 | TCTAGTTGCATTGTG[A/G]TTTTATTATAGGTTT | 56916 |
rs576574131 | in-del | -/AG | | | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290590 | TACAGGACCGCCTGA[-/AG]AGAGAGAGCCATTGT | 56916 |
rs576625220 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244156 | TCAAGACCAAAGGGT[G/T]AAAAACTTAAGGAAC | 56916 |
rs576730650 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94205955 | GGCGCCCGCCACCAC[A/G]CCCGGCTAATTTTTT | 56916 |
rs576774627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238598 | AGCCTGAGTGACAGA[A/G]CAAGACCCTGTCTCA | 56916 |
rs576784768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230871 | TTCAGAAGGACAGGC[C/T]GAAAGGTAAAAGGAA | 56916 |
rs576801970 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254361 | AGAGTTGGGTTGCTC[A/T]GGCTTGTTGAGATTC | 56916 |
rs576865619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94253325 | CATTTAGGAAGGAGT[C/T]GTTTGCTAGCCTGTT | 56916 |
rs576873084 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281284 | AGGCAGTTTATTCAT[A/T]TATAGGCTGCAATAA | 56916 |
rs576887388 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235461 | TAGGTGGTCCTGTGC[C/G]TGCCAGTTTAAGTGT | 56916 |
rs576892726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247069 | CTTACATTGGGATGG[A/G]ATGGTGGTGTCAATA | 56916 |
rs576952257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212806 | AAATAGGACCTTAAA[A/G]TAGTCCCTTTAGCCA | 56916 |
rs576960663 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286788 | ATGTTCACCTACATT[G/T]TCTGTTAAAATAGCA | 56916 |
rs576989450 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219139 | TCTTCTAAGAGGGCA[A/C]ATATATGATGTGTTT | 56916 |
rs576995862 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212295 | TTCTCATACCTCAGC[C/T]TCCCGAGGAGCTGCG | 56916 |
rs577001375 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275971 | CCCGGCTAATTTTTT[A/G]TATTTTTAGTAGAGA | 56916 |
rs577004897 | snp | C/T | | | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94253176 | TTTCAAATAGTGTCA[C/T]ATGACCTAATTTTGA | 56916 |
rs577015388 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281833 | CAAGACTACCCTGGA[A/C]AACATGACAAAACCC | 56916 |
rs577019452 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213935 | TACAATAAAAAACAT[C/T]ATTTGACAATGGGCA | 56916 |
rs577030181 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245498 | AGGAGGCTGGCAACA[A/C]CACAGAAATTTTATT | 56916 |
rs577058645 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226265 | AATACAGTTCAAGAG[A/G]AAACATTCAACAAAG | 56916 |
rs577066660 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229632 | TTCTGGTTCTTTTTA[A/G/T]TAGGAAATGATACTT | 56916 |
rs577088210 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260202 | TTAAATGCACCCACC[A/G]ATATTATTACATAGT | 56916 |
rs577089635 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94251875 | TATTTTTTTTGAGAC[A/G]GAGTCTTGCTCTGTC | 56916 |
rs577149327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259626 | CCTTAACTGTTAAAG[C/T]GTCCTGAAGTAAGAA | 56916 |
rs577196453 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214272 | GTTCTTTTGTTTTTT[G/T]TTTTTTTTTTGAGAC | 56916 |
rs577210497 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256616 | GATCCACCTGTTGCG[A/G]CCTCTCCAAGTGCCG | 56916 |
rs577244201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271585 | AGAAAGTAATCTTTA[A/G]CATTGTAAGATATTT | 56916 |
rs577285365 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220889 | AATACTTTGTGAAAC[A/C]AAATGTGAAGTACGC | 56916 |
rs577346801 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240539 | TGGTTTCTGTGATGG[A/T]ATTCAGATAACTTAC | 56916 |
rs577365839 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277402 | TTTTCTGAAGGATGA[C/T]GATTTTAAATTGATG | 56916 |
rs577393391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269102 | TGCTTTTTCTCCTAC[C/T]TATACTTTTAGTTGT | 56916 |
rs577483396 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220648 | TCATAATAATATTAA[C/G]ACACTACTTGCCTTT | 56916 |
rs577484595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260405 | CTGGAGTGCAGTTTC[A/G]TGATCTTGGCTCACT | 56916 |
rs577485823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269812 | TAGCTGGGACTACAA[A/G]CATACGTCACCATGC | 56916 |
rs577503202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277587 | CTGAAATAAAAGTTC[A/G]TAAAACCAAAGTCAC | 56916 |
rs577519304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276956 | TCACCTTTCACTGGG[A/G]AGGATAGACATGAAA | 56916 |
rs577575298 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229205 | GTAATAGTCCTATTC[C/G/T]CTAGCCAGCTTTCAC | 56916 |
rs577583797 | snp | C/G | 0.00203873 | 0.0318624 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94290961 | ACTGAGAACTCACGG[C/G]TTAACCCCAGTCTTG | 56916 |
rs577617115 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264137 | ATATCTCTCCGTGTG[A/T]TAGTCTGTTTAGAAG | 56916 |
rs577636283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208877 | TATTGGAAGAGCGAT[A/G]TCAGTGATTCAGTCC | 56916 |
rs577675293 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215494 | GGTGTGGTGGTGTGC[A/T]CCTGTAGTCCTAGCC | 56916 |
rs577724832 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233734 | TCCATCCCAGCTCAG[A/G]GTTGAGATTTTTTCA | 56916 |
rs577750662 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221431 | CACCTGTCAAGTTTG[G/T]GTTTAGTATCAAAGA | 56916 |
rs577764494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241213 | GCACAGACTATTTTG[C/T]GTCTGTGGATATCAG | 56916 |
rs577871553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283804 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 56916 |
rs577893263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234404 | TAAAATGCATAACCT[C/T]CCCATTTCCATTAGA | 56916 |
rs577932306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284895 | TTGAACTCTTAAATA[C/T]AGTTTACATATATCC | 56916 |
rs577961323 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236352 | AGCAGTATAAAAACA[A/G]TATATTAGAATGATG | 56916 |
rs577994694 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235694 | ATGAGGGCTAAAGTA[C/T]TTTAAAGCAGTAATA | 56916 |
rs578064814 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246227 | CGGGTTCAAGCAATT[C/G]TCCCACCTCAGCCTC | 56916 |
rs578071105 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243344 | AGACATCTGCACATG[A/C]AATTTATTTGTGTCT | 56916 |
rs578145899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94279204 | GGTTCTGTTGCCAAG[A/G]CAGGCAGTCTGGGCT | 56916 |
rs578214282 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291740 | TTTGTGTGACCTTAC[A/G]TGTGATACTTCACAG | 56916 |
rs578235298 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247872 | TATGTTAGAATTGGG[C/G]TACATGTGCAAGTTT | 56916 |
rs578239251 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272167 | TTTCTTCTTACAAGG[A/G]CAGTCATATTGGGTT | 56916 |
rs578241532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242533 | AGTTGTACACAGGGC[C/T]ACTCTCTGAGTTGGG | 56916 |
rs745309641 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212476 | CACCACGCCCAGCCC[C/T]ATACATATTTATTTA | 56916 |
rs745339200 | snp | A/G | 1.66813e-05 | 0.00288797 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94278430 | TGCTCAGAAATCAGC[A/G]GATGAGCAAAGCATA | 56916 |
rs745419051 | snp | A/G | 1.65113e-05 | 0.00287322 | missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208576 | ATTCAGATATAACTG[A/G]AAAAACAGGTGAGTT | 56916 |
rs745434721 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217921 | TTTCTTTCAGTTACA[C/T]TTGCAAATCTAACAA | 56916 |
rs745439898 | snp | C/T | 3.29755e-05 | 0.00406038 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277183 | AAATGCATATTTTCT[C/T]CCAAATATGTTATTT | 56916 |
rs745441487 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282351 | TCCGCCCGCCTCGGC[C/T]TCCCAAAGTGCTGGG | 56916 |
rs745463984 | snp | A/G | 1.65696e-05 | 0.00287828 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94264731 | ATGTCCAAAACTAAT[A/G]GCTTATCAGAAGATT | 56916 |
rs745466770 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234132 | CTTAAGGTTATATTC[A/C]TTGGTTATTGTAGCT | 56916 |
rs745488622 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230493 | TGGGCATTTTGGTTA[C/T]CACAGTTTCTTAAGC | 56916 |
rs745572334 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94290976 | CTTAACCCCAGTCTT[A/G]ATGGTATATTGAACA | 56916 |
rs745648310 | snp | C/T | 0.00016621 | 0.00911467 | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208178 | ATTTTAAAAGATACC[C/T]CCGTCCACCTTCTAA | 56916 |
rs745664008 | snp | C/T | 1.76886e-05 | 0.00297389 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281636 | ATAACTCATTTATTA[C/T]TATTGTTAGGATTTT | 56916 |
rs745664747 | snp | C/T | 1.65015e-05 | 0.00287237 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94236974 | AATCAACAAGCACTA[C/T]GGATGGAGCAATTGC | 56916 |
rs745692165 | snp | C/T | 6.59696e-05 | 0.00574286 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281432 | CTTTGAGTAGTAAAA[C/T]GATTTTTTCTATTTC | 56916 |
rs745698519 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277440 | CAGATATATAGTATG[C/T]GCGGAAAGTTTGATC | 56916 |
rs745719477 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231177 | GTTTTTTGTTTGTTT[G/T]TTTTCTTGCTGCTGT | 56916 |
rs745749484 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241066 | TTAGGATATGTGGAG[-/T]TTTGTGGATATTATT | 56916 |
rs745752574 | in-del | -/TAT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256095 | ACAGTAGGGAGGGGA[-/TAT]TATTATGTCTGTGAA | 56916 |
rs745764104 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284578 | AATTTTGGTTTTTGT[G/T]TTTTTTTTTTTTCGT | 56916 |
rs745797386 | in-del | -/TTCT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285437 | AAAAATAAACACGTG[-/TTCT]TTCTTTTATGGGAGA | 56916 |
rs745798343 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284896 | TGAACTCTTAAATAT[A/C]GTTTACATATATCCA | 56916 |
rs745803425 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254396 | TTATTTAATAAGATA[C/T]GCAATTATCTGCACT | 56916 |
rs745803881 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248739 | CTTCTTTAGTCCAGA[C/T]ATCCATAGCATTTTA | 56916 |
rs745900514 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226631 | GCTTTATGATTTATT[C/T]TAAAGTCCATGAATC | 56916 |
rs745911341 | in-del | -/ATA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266967 | TAAATTGTTTAAAAT[-/ATA]ATACAGTGAGGAAAA | 56916 |
rs745941235 | snp | C/T | 1.86298e-05 | 0.00305197 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252744 | AAAGCACAAAATGGC[C/T]TTAACAAGAAACGTA | 56916 |
rs745962271 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238070 | TACAAAAATACAAAA[C/T]GATGTGTTCCCATGG | 56916 |
rs745963007 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286172 | AAGAGAGGTAGGGAG[A/T]GAGGTGGTATGAGAA | 56916 |
rs746057422 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214092 | AGTGGGGACTGATCA[C/G]TGACCAGTTTCCTTG | 56916 |
rs746082279 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227484 | TAGTGCCTGTGGGAG[A/G]GATAATAAGTGGTTA | 56916 |
rs746083531 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272419 | GTTGCAGTAAAATGT[A/G]CAAATATACAGCTTA | 56916 |
rs746083580 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256096 | CAGTAGGGAGGGGAT[A/G]TTATTATGTCTGTGA | 56916 |
rs746108780 | snp | A/G | 0.000162588 | 0.00901486 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290055 | AGCAGATGTTCACCA[A/G]TGTCAGCAAGAACTC | 56916 |
rs746172393 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246213 | CAACCTCCGCCTCCC[A/G]GGTTCAAGCAATTCT | 56916 |
rs746186398 | snp | C/T | 4.9423e-05 | 0.00497082 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94270782 | GCTGGCATTGGTACA[C/T]AAACATGGACTTAAT | 56916 |
rs746248597 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245176 | AAACAGTTTGGACTC[A/G]GAGCAGTCAAAAATG | 56916 |
rs746290982 | snp | A/G | 9.94349e-05 | 0.00705036 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94279002 | TTTATTACATCGCCA[A/G]TATTACACAGCTGAA | 56916 |
rs746310337 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280443 | TTATACCTAAAAGAT[G/T]AATACTAATTTTCCT | 56916 |
rs746315276 | snp | A/G | 1.64917e-05 | 0.00287151 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94283280 | ACAAGCAGAAGATAG[A/G]TGCCATAGAGTAGGC | 56916 |
rs746331228 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233821 | AAAAGGTCTCTTTCT[G/T]ACAAGTATAGATTGC | 56916 |
rs746399505 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290098 | AAGGTGGCATTCCAT[A/G]TACTAACATCCCCCA | 56916 |
rs746451597 | snp | G/T | | | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209398 | CAAGTCCTGGCAGTA[G/T]GATTCCTGAGCATAA | 56916 |
rs746504711 | snp | A/G | 1.64879e-05 | 0.00287118 | missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208431 | CGTTTTCGCTTTGAG[A/G]AAAGGAATAAGATTG | 56916 |
rs746506599 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215953 | TATCTTAAATTCCAC[A/G]TGTCTTAGTCTGTTA | 56916 |
rs746524829 | snp | C/T | 3.35762e-05 | 0.00409719 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208339 | TCTCTTTATTTTTCC[C/T]CTGCAGATAGTTCAT | 56916 |
rs746562700 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230898 | GAAAATCAGAAGTAA[-/T]TGTTGCAGAACCCCT | 56916 |
rs746573545 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290357 | TGCTCCAATTCTCTT[-/C]CTCTCTAAATAGTAG | 56916 |
rs746599291 | snp | C/T | 1.648e-05 | 0.0028705 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277171 | GACAGTAAGCATAAA[C/T]GCATATTTTCTCCCA | 56916 |
rs746616116 | snp | C/T | 1.64855e-05 | 0.00287097 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252934 | TTGGTGAACTTACTT[C/T]GATTCCTCAGTGTTC | 56916 |
rs746622908 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264107 | ATTGGTCATAGTTAA[C/G]TTTTGATTCATGTGA | 56916 |
rs746627755 | snp | C/T | | | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252401 | GATTTATATTTAATT[C/T]ATTTTAAAAACAAGT | 56916 |
rs746644225 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261294 | AGTACACATTTTACT[G/T]TTTATCTGTTTCTCA | 56916 |
rs746688556 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210258 | GGCTTCGGGAAATAA[C/G]AAAACTAAGTTTGTT | 56916 |
rs746714776 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250550 | AAAATGTCAAGTTTT[A/C]TTTCCTTTGAAGACT | 56916 |
rs746788886 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94280690 | TAAACAGTACCGACA[C/T]ATTAATAACTTTCAG | 56916 |
rs746791930 | snp | C/G | 2.52599e-05 | 0.00355377 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94234103 | TTTTTCCACAAAGAA[C/G]TGACAATGATTTACT | 56916 |
rs746793279 | snp | A/G | 1.71062e-05 | 0.00292451 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233940 | GTTTTTTGCTCCTCT[A/G]AAAATATTTTTAGTT | 56916 |
rs746810148 | snp | C/T | 0.000173958 | 0.00932464 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94253271 | TCCTTTGCATAGAAA[C/T]TTCGTTCATTTCACT | 56916 |
rs746816305 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229012 | TGATCTTGTGTCGTC[C/T]TCAGTGTGTCATATC | 56916 |
rs746855496 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290515 | TAGGTACTGCATGGA[A/C]ATAGGTCATTAACTT | 56916 |
rs746913288 | snp | C/T | 1.6643e-05 | 0.00288465 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280829 | TCTCAATTACTTTAA[C/T]TTCTTAAAGCAATTC | 56916 |
rs746932877 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236753 | AACCTGATACATTTT[-/A]AAAATATGCTTAAAA | 56916 |
rs746944244 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260174 | TACTTTCTGTAAAAC[A/G]ATCATTAGAAGGTTA | 56916 |
rs746945567 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218200 | TATTATTTAGAAGTC[C/T]CTCCTTTAGGTTTAA | 56916 |
rs746971671 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279792 | TCTTTATTTTTGCCT[C/G]TTTCTCCTTTAACAT | 56916 |
rs747000640 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258944 | TAGCCATATTGAATC[A/G]AACTTTCTAAAATCA | 56916 |
rs747005769 | snp | A/T | | | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206370 | GAGGTCATTATATTA[A/T]AGGAAATAAGGCAGG | 56916 |
rs747010114 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236420 | TCAGACAATTCAGAA[A/G]TAGAGTAAAAATTAA | 56916 |
rs747019757 | in-del | -/AG | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288204 | TCTAAGAAAATAAAC[-/AG]AGTAATTTTCAGACA | 56916 |
rs747026294 | snp | A/G | 1.66563e-05 | 0.0028858 | splice-acceptor-variant | SMARCAD1 | GRCh38.p7 | 4:94250750 | AAATGACTTATTTCT[A/G]GGAACTTAGAGAAGT | 56916 |
rs747037473 | in-del | -/AATA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276911 | GAATGTTAAATTATT[-/AATA]ATGGTTTTAATTTAT | 56916 |
rs747063122 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247989 | TTTTCCTTAACTCTT[A/C]CCCCACATCCTCCCT | 56916 |
rs747087651 | snp | A/G | 0.000183705 | 0.00958222 | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208129 | GAGGGGCGGGCGGGG[A/G]AGGCGGACGAAGGGG | 56916 |
rs747111755 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246995 | TGGAGTTTGATTGTT[C/T]ATGATACTCTTAAAT | 56916 |
rs747158284 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275319 | TCTGTAATAAATACA[A/G]TGAAATTTCATTTTC | 56916 |
rs747177988 | snp | G/T | 1.68343e-05 | 0.00290118 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208610 | ATGTTAAAATTGATG[G/T]AACATCAAGGACAGT | 56916 |
rs747188565 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269905 | CGCGAACTCCTGAGC[A/T]CAAGCAATCTGCCCA | 56916 |
rs747200696 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224946 | TAAAGATTCAACTGG[C/T]CATTGCTTTTTAAAA | 56916 |
rs747209047 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272766 | GATCTTCTTCTGTTG[G/T]ATATGAATATTTAGG | 56916 |
rs747378154 | snp | A/C | 0.000162588 | 0.00901486 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290022 | AGATTATATAGCTTT[A/C]ATTTTATTGCTATTT | 56916 |
rs747392754 | in-del | -/AATA | 6.60611e-05 | 0.00574684 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274853 | AATAAAGTACAGCAC[-/AATA]AATAGTCATGTGTTT | 56916 |
rs747424560 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254050 | TGTCTTGAAGTGGCA[A/T]TAGGGGAGAGTCCCT | 56916 |
rs747442635 | in-del | -/TTTG | | | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94251433 | TTTGGTTTGGGTTTT[-/TTTG]TTTGTTTGTTTTTAA | 56916 |
rs747468692 | snp | A/G | 3.33028e-05 | 0.00408048 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278566 | GTTTTTAAAACTTAG[A/G]TTTTTCTCTTTACTA | 56916 |
rs747508295 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244829 | CAAAAGCAGAATTCA[A/G]CCTATGTCACATTCT | 56916 |
rs747543967 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214698 | GCAAAAGAATAAAGA[C/T]ATATTTTCCCTGGGG | 56916 |
rs747563237 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243760 | TATCCACTGGCTGCC[C/T]CTTTTTACCATGTAT | 56916 |
rs747588872 | in-del | -/TT | 1.65326e-05 | 0.00287507 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237053 | AGCCATGTCGATTTA[-/TT]TTGTTACGTCATAAT | 56916 |
rs747644368 | snp | A/G | 1.65266e-05 | 0.00287455 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94283193 | AACAAAAGCTGGTGG[A/G]TTAGGAATAAATCTG | 56916 |
rs747650964 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220374 | CACCTCAGCCTCCCT[A/T]GTAGCTGGGACTACA | 56916 |
rs747651433 | snp | C/G | 4.25089e-05 | 0.00461006 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241056 | GCTGCTTAAGGTTAG[C/G]ATATGTGGAGTTTGT | 56916 |
rs747659327 | in-del | -/A | 8.36785e-05 | 0.00646779 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226348 | GTGAGATTTTCCAAG[-/A]AAAAAAACCTACCTA | 56916 |
rs747669468 | snp | C/T | 1.83242e-05 | 0.00302684 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240889 | CAAAGTTTGAGTGTG[C/T]TGCTCTGCTTTAAAA | 56916 |
rs747690168 | in-del | -/AAA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210929 | CAGAGACTGTATCTC[-/AAA]AAAAAAAAAAAAAAA | 56916 |
rs747728204 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279387 | TCAAGCGATTCGCCC[G/T]CCTTGGCCTCCCAAA | 56916 |
rs747731013 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221863 | ATCAGAAGAACTGAC[C/G]AAAGCAAGATGCTTT | 56916 |
rs747731793 | in-del | -/TG | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240019 | TACTCTGCTTTAAAA[-/TG]TTAATAACATTCCAT | 56916 |
rs747733445 | snp | C/T | 1.65545e-05 | 0.00287697 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94284974 | GAGAAGTACTAGTTA[C/T]AAAACTAATAAGCCA | 56916 |
rs747766087 | snp | C/T | 1.64961e-05 | 0.00287189 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94276423 | TTTTGATGAGGGCCA[C/T]ATGCTGAAGAATATG | 56916 |
rs747802571 | snp | A/G | 1.684e-05 | 0.00290167 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208331 | TTTTTTCCTCTCTTT[A/G]TTTTTCCCCTGCAGA | 56916 |
rs747896544 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239993 | GTGGTTAGTGTTTGT[A/G]GTGACACAAATACTC | 56916 |
rs747912885 | snp | A/G | 1.711e-05 | 0.00292484 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252768 | AAACGTAAAAAAAAT[A/G]TTTTTAATCCAAAGA | 56916 |
rs747959104 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250398 | AATATTGGTTCTTTA[C/T]CTTTGTTGAAACTAC | 56916 |
rs747964466 | snp | C/T | | | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209292 | GTCATTTAATTTGCA[C/T]AATAATCCTACAAGG | 56916 |
rs747973319 | snp | A/G | 4.96602e-05 | 0.00498274 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276971 | GAGGATAGACATGAA[A/G]GGAGTGGCTCTTTAA | 56916 |
rs747995328 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213522 | CTGTGTCAGGGACGG[C/T]AGATCTTATTTGGTA | 56916 |
rs748022972 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215560 | CAGGAGTTTGAGGTT[A/G]TGGTAAGCTGTGATC | 56916 |
rs748035338 | snp | C/T | 0.000163252 | 0.00903323 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94290923 | CAAATAAAACTCTTA[C/T]AGTGATTATTTAGAT | 56916 |
rs748046221 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236242 | CTTATTTAAAAGTAA[A/G]ATCTTTTTAAAACAA | 56916 |
rs748053371 | snp | G/T | 1.64735e-05 | 0.00286993 | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94279101 | ATAAGAGGTTAAGTT[G/T]TTAGGCTATAAGATT | 56916 |
rs748055580 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257656 | TACTTAGATTAACAA[A/G]TAATTCTATAGGCTT | 56916 |
rs748148546 | snp | A/G | 3.35548e-05 | 0.00409588 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94273675 | TCTATCAGGAGGGTA[A/G]TAATGGTCCTCATTT | 56916 |
rs748164244 | in-del | -/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221200 | CATTTCTGAGAAGAT[-/C]AATGGTGATATTAAC | 56916 |
rs748179381 | snp | A/G | 1.66988e-05 | 0.00288949 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94234041 | ACTGGAAGACCTTTC[A/G]GAATTGGAAGACCTT | 56916 |
rs748222339 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207705 | TTTTTTATTTTCAAC[C/T]TTTGTTACATAGCAC | 56916 |
rs748223883 | snp | A/G | 1.64827e-05 | 0.00287073 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94280669 | CTTCGAACTACATGT[A/G]CTTTGTAAACAGTAC | 56916 |
rs748230229 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267910 | ATATGATTATATAGC[A/C]TCTAAATATTAGAAC | 56916 |
rs748232457 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229902 | TTTCTTCTGACAGTG[A/C]GAACCCTGACTTCTA | 56916 |
rs748275172 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231905 | CTTGCTCTGTTACCC[A/G]GGCTGGAGTGCAGTG | 56916 |
rs748335254 | snp | A/G | 4.94743e-05 | 0.0049734 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94249696 | TCTAGCAGTAATTGG[A/G]AAAAGCAGGAAAGTA | 56916 |
rs748356632 | in-del | -/ACTC | | | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289704 | CTGAATTCTCCAAAT[-/ACTC]ACTCACACGTGAAAT | 56916 |
rs748357777 | snp | C/T | 1.64795e-05 | 0.00287045 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94274760 | GTTAAGGGAAGTTAA[C/T]TTATGGTGCCCTACT | 56916 |
rs748372017 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234909 | GAGACTAGTATACTA[G/T]AGAGTACATATTCTT | 56916 |
rs748446890 | snp | C/T | 8.94414e-05 | 0.00668676 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289679 | TAGTATGGACAACTT[C/T]TTGCCACTAACTGAA | 56916 |
rs748491250 | snp | A/G | 4.94719e-05 | 0.00497328 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277186 | TGCATATTTTCTCCC[A/G]AATATGTTATTTGTG | 56916 |
rs748494146 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283996 | TTATTTTAGATGAAT[C/G]GTACATTTTGACATT | 56916 |
rs748529019 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208473 | GAAGCAACCCCTCAA[C/T]CTTCCCAGCCTGGCC | 56916 |
rs748531196 | snp | C/T | 5.09489e-05 | 0.00504697 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250722 | GCTAATTTGAGATTT[C/T]TAACAAAAAGATAAA | 56916 |
rs748562061 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221462 | AAAATATTCACAATA[A/G]TCTAAAAAGGCTATG | 56916 |
rs748564652 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267926 | TCTAAATATTAGAAC[C/T]AACTAGAAAAGAATA | 56916 |
rs748616166 | snp | A/C | 1.66596e-05 | 0.00288609 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278525 | AAGAAGAGGTAATGC[A/C]TATCTACATGTTTTT | 56916 |
rs748655356 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269612 | GTATAATAGATGTTC[A/G]ATAAGTGATAACTGT | 56916 |
rs748656676 | in-del | -/AT | 1.6525e-05 | 0.00287441 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274864 | GCACAATAAATAGTC[-/AT]GTGTTTATTGTTTTT | 56916 |
rs748661374 | in-del | -/ATTA | 5.80366e-05 | 0.00538655 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280544 | TTTTCTCATCATATT[-/ATTA]ATTATTTTTATTTTG | 56916 |
rs748713054 | snp | C/G | 3.83929e-05 | 0.00438121 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226071 | AACTAACAACAGATT[C/G]GTTTTCCAGTTGCTC | 56916 |
rs748772735 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258149 | AAATTTCCCATCAGA[-/T]TTTTTTTTTTTTCTT | 56916 |
rs748780894 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231364 | CTAGAATGCCTTAGC[A/G]GTGAGAGGGGACTTT | 56916 |
rs748810392 | snp | A/G | 1.65293e-05 | 0.00287479 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94264785 | ATCCAAGAAAGAGAT[A/G]TAGTTATAAGGCTTA | 56916 |
rs748830361 | snp | A/T | 1.64958e-05 | 0.00287187 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94236993 | TGGAGCAATTGCTGC[A/T]GCCTTGCTGATGTTT | 56916 |
rs748851771 | snp | C/T | 4.53988e-05 | 0.00476417 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283087 | CATTATACAACTTTT[C/T]AGTGAGATTTAACCT | 56916 |
rs748895835 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256456 | CAACCTCCACCTCCC[A/G]GGTTCAAGCGATTCT | 56916 |
rs748928510 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220500 | TGATCTGCCCGTCTC[A/G]GCCTCCCAAAGTGCT | 56916 |
rs748934782 | in-del | -/TT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240353 | CTATGTTATATTCTC[-/TT]GTTTTTACATTAAAA | 56916 |
rs748936676 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219564 | TAAGATTGTCTTCTT[A/T]TATGCATACCACTCA | 56916 |
rs748943416 | snp | C/G | 5.98844e-05 | 0.00547162 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240869 | GATTTTTTGCTATTT[C/G]TGTGCAAAGTTTGAG | 56916 |
rs748944458 | in-del | -/TTGG | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234133 | TTAAGGTTATATTCA[-/TTGG]TTATTGTAGCTGTAA | 56916 |
rs748954002 | in-del | -/CT | 1.64882e-05 | 0.00287121 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270713 | TGTAATATTTGGTAA[-/CT]CTCTCTTTACCAGTT | 56916 |
rs748999308 | snp | A/G | 0.000145148 | 0.00851781 | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208192 | CCCCGTCCACCTTCT[A/G]ATTGTTGCGGCCTAA | 56916 |
rs749070489 | snp | C/T | 9.49623e-05 | 0.00689 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208252 | CCACTGGCATGTTTG[C/T]GGGCCCTTTATTGCC | 56916 |
rs749076338 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222672 | TTAAAGGTTAATTTT[-/A]AAAATTGAGGCTGGG | 56916 |
rs749092353 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213217 | AGGGCAAAATACTAA[G/T]CAAAGTAGAATCACT | 56916 |
rs749095974 | snp | A/G | 3.38043e-05 | 0.00411109 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276292 | TTTCACTAGACTCCA[A/G]GCTCTTAAAGGTATA | 56916 |
rs749104805 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262852 | GACAGGGCTGTGTCT[A/G]TCTCCCAGATAATTC | 56916 |
rs749140922 | in-del | -/AGG | | | cds-indel, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94233984 | AGATGAAGAGTCCCA[-/AGG]CCTTCCTACCATGGC | 56916 |
rs749147256 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211164 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAAGCAG | 56916 |
rs749176913 | snp | C/T | 5.34869e-05 | 0.00517113 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252756 | GGCTTTAACAAGAAA[C/T]GTAAAAAAAATGTTT | 56916 |
rs749199135 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258407 | TGATCCGCTCACCTC[C/T]ACCTCCCAGAGTGCT | 56916 |
rs749200696 | snp | C/T | 0.000162377 | 0.00900901 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290117 | TAACATCCCCCAGGT[C/T]CTCTCAAGTACTTCT | 56916 |
rs749255462 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232466 | CAGGGAATATAGAGA[A/G]GCATAATGAAAATTC | 56916 |
rs749257503 | snp | C/T | | | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209186 | ATTAAGATTTCCACT[C/T]GAATCTATGTTCATT | 56916 |
rs749292618 | snp | C/T | | | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94249683 | TGAGTCTGCAGAATC[C/T]AGCAGTAATTGGGAA | 56916 |
rs749301001 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286328 | TCCAAAGAGAATAAA[C/T]CTTCAGTTTTATACA | 56916 |
rs749336230 | snp | C/G | 3.29571e-05 | 0.00405924 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252866 | TAGTGGTGAAGAAGT[C/G]ATGGAGGATGGCTAT | 56916 |
rs749356198 | snp | C/G | 3.32055e-05 | 0.00407451 | missense, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94279039 | AAGGAAATGTCTCAG[C/G]TTATGCTAAAGGTAA | 56916 |
rs749358298 | snp | A/G | 1.90123e-05 | 0.00308315 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233911 | TGAAATAACATTAGT[A/G]ATACATTAAAAATGT | 56916 |
rs749360568 | in-del | -/TAAG | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277274 | TCTATGAAGTAACTT[-/TAAG]TAGGTGATAACTCTA | 56916 |
rs749367981 | snp | A/T | 0.00016368 | 0.00904505 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290540 | TAACTTGAAACTCTT[A/T]TCAAAATATATTTTA | 56916 |
rs749379015 | snp | C/T | 1.65051e-05 | 0.00287267 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226247 | GTTTCCCCAAATTGC[C/T]CCAATACAGTTCAAG | 56916 |
rs749381261 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227647 | GGTACTGAGATAAAG[A/G]TGACTGTTTCTGCTG | 56916 |
rs749395989 | in-del | -/A | 0.000101858 | 0.00713573 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281614 | ATTCATGTTAGTTAC[-/A]AAAAAAATAACTCAT | 56916 |
rs749418898 | snp | C/T | | | intron-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94253546 | GTCTCTAACATGTTT[C/T]TGTTGGTTAAGCAAC | 56916 |
rs749472057 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281627 | ACAAAAAAATAACTC[-/A]ATTTATTATTATTGT | 56916 |
rs749474866 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225655 | GCTGGCTATGTGCCA[A/G]TTACTGAACTAAATG | 56916 |
rs749482681 | snp | C/T | 1.64825e-05 | 0.00287071 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270828 | GAAATGGTAAGTGTA[C/T]TTTATTTCTAAGATT | 56916 |
rs749487432 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216601 | AAACTCTTTATGCAT[C/T]GAACAACTACTCCTC | 56916 |
rs749503334 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258591 | CATTTTGAGTCTCTT[A/G]TTTCTGAATTCAGTG | 56916 |
rs749519571 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246279 | TGCCTGCCACCACGC[C/T]TGGCTAATTTTTTGT | 56916 |
rs749659664 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245408 | GATAATGGCTTTACT[C/G]CTGAAGATATTAGGA | 56916 |
rs749662289 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224597 | TTTTAGAACATTTTT[-/T]ATTTTGGGTTTTTGG | 56916 |
rs749684131 | snp | A/G | 1.67713e-05 | 0.00289575 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94273663 | TTCTGGCATACCTCT[A/G]TCAGGAGGGTAATAA | 56916 |
rs749688175 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247169 | GATTTGGTGTTTCCT[A/G]TAATAGTAGCCCATA | 56916 |
rs749713437 | in-del | -/ATG | 1.65149e-05 | 0.00287353 | utr-variant-3-prime, nc-transcript-variant, cds-indel | SMARCAD1 | GRCh38.p7 | 4:94289602 | AAGGACATTTACATT[-/ATG]ATGACCATGGGGTTT | 56916 |
rs749737891 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223497 | GACTCTGTCTCAAAA[A/G]TAAATAAATAAATAA | 56916 |
rs749755207 | snp | A/G | 1.65132e-05 | 0.00287339 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289483 | TACAGGTGATGAAGG[A/G]AGTATGCCAGCAGAT | 56916 |
rs749767872 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267155 | AGCTAAATCTGCCAA[C/G]GTTCTTCTGATCTTG | 56916 |
rs749787825 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267405 | TGGTCGGACAGCATC[C/T]GTAACCTGTTTTCTA | 56916 |
rs749812122 | snp | C/T | 1.64936e-05 | 0.00287168 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94284998 | TAAGCCAAGGGACGA[C/T]TGAAGAATCCATGCT | 56916 |
rs749813218 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208453 | ATAAGATTGAGGAAG[C/T]GCCCGAAGCAACCCC | 56916 |
rs749912661 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285615 | GACACTGTTATGTCT[A/G]TGTTATATTAGGCAC | 56916 |
rs749929040 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258258 | CTCCCACGTATAAGC[A/G]ATTCTCCTGCCTCAC | 56916 |
rs749930466 | snp | C/T | 0.00211928 | 0.0324831 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289801 | CTGAATGGGGATTAG[C/T]TGGTGATTGTTTGTA | 56916 |
rs749944749 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269252 | GAGTTTGATCCTTCA[A/G]CAATTTATTATACTA | 56916 |
rs749947951 | in-del | -/AGATA | 0.000163948 | 0.00905246 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94290935 | TTACAGTGATTATTT[-/AGATA]TTAAAGACTGAGAAC | 56916 |
rs749983610 | snp | A/C | 1.91243e-05 | 0.00309221 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289634 | TATGAACATTTATAA[A/C]TTTTTATAATTTCCA | 56916 |
rs750006571 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271463 | ACTTTTTTGAAGTGT[A/G]TATTTAAAATGAGTC | 56916 |
rs750056186 | in-del | -/A | 1.6473e-05 | 0.00286988 | frameshift-variant, splice-acceptor-variant, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94278928 | CTCTTTGAGTCACAG[-/A]AAAAAAACACAGAAA | 56916 |
rs750173422 | snp | C/T | 3.30393e-05 | 0.0040643 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270692 | AAACTGATAGAAATA[C/T]AGATGTGTAATATTT | 56916 |
rs750178747 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232282 | ATTTATTACATCATG[A/G]GGCACATGAATTTGT | 56916 |
rs750227099 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256600 | ACTGCTGACCTCAGG[C/T]GATCCACCTGTTGCG | 56916 |
rs750236630 | snp | C/T | 1.66114e-05 | 0.00288192 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94264888 | GGAACATAGAACAAC[C/T]TTCCATTCTAAACCA | 56916 |
rs750261494 | snp | C/T | 3.35362e-05 | 0.00409475 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94283151 | TGAGTTTAATACCGA[C/T]ATGGATATCTTTGTG | 56916 |
rs750269147 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214540 | TAAAGTGCTGGGATT[A/G]CAGGCATGAGCCACC | 56916 |
rs750312433 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262584 | AGAACGCATTAAAAT[C/G]ATTCATACCCTTACT | 56916 |
rs750318368 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222359 | TACAACTGACATAAG[A/G]AAAAACTCTTTGGGA | 56916 |
rs750334401 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286385 | GGCAAGCTTTAGACA[A/T]CTTACCTGTTCAAGC | 56916 |
rs750430189 | snp | A/G | 1.85572e-05 | 0.00304602 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241021 | TGTAAGTTTACATTT[A/G]AATTACAGTATCAAA | 56916 |
rs750463058 | snp | A/G | 4.98269e-05 | 0.00499109 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208366 | TCATTTAAAGCCCCC[A/G]TCCCTGCAAGGTGGT | 56916 |
rs750498665 | snp | C/T | 0.000105103 | 0.00724847 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276507 | AAGTTTTCCAAATTA[C/T]TGTAAAATTTAGATT | 56916 |
rs750514840 | snp | A/G | 1.64846e-05 | 0.0028709 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94276371 | GCAGTTCTGATGACC[A/G]TAGTCTGTTTCGACG | 56916 |
rs750517326 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264374 | AATGTTTTTAAAAAC[C/T]TGATAGGAGATAGTA | 56916 |
rs750527853 | in-del | -/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225304 | CTTGGCTTGTAAGGT[-/G]GATCTCCTTCCTGCC | 56916 |
rs750554739 | snp | C/G | 1.69902e-05 | 0.00291458 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208309 | ATCGTATATTGTTTT[C/G]ATGGCCTTTTTTCCT | 56916 |
rs750589068 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241136 | AACTAAGGGAATTTA[C/T]GTCTACATTTAATTT | 56916 |
rs750609543 | in-del | -/TCC | 0.000190494 | 0.00975761 | intron-variant, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94213126 | ATGAGTGAAGCCTGA[-/TCC]TCCTCCAAGAGCACC | 56916 |
rs750625153 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240612 | CACTTGGAAGAATCC[C/T]TCCCTCCTAATGTTG | 56916 |
rs750689203 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280471 | CTTGATAAGTCTGTT[-/A]ACACTAAAAGGTTCT | 56916 |
rs750694296 | snp | C/G | 1.64838e-05 | 0.00287083 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252834 | GATGTCGGTAGTTCA[C/G]TAGATGAGGACTATA | 56916 |
rs750703228 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287321 | GATGATAATACATGT[A/G]TGCCCTTCTTTCCAT | 56916 |
rs750745764 | snp | C/G | 1.65397e-05 | 0.00287569 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94234000 | GGCCTTCCTACCATG[C/G]CACGTAGAAATGATG | 56916 |
rs750770346 | snp | G/T | | | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206381 | ATTAAAGGAAATAAG[G/T]CAGGCACAGAAAAAA | 56916 |
rs750775591 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258378 | CGGGCTGGTCTTGAA[C/T]TCCTGACCTCAAGTG | 56916 |
rs750787207 | snp | A/G | 1.66299e-05 | 0.00288352 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226336 | TATTTGCATGTGTGT[A/G]AGATTTTCCAAGAAA | 56916 |
rs750814290 | snp | A/G | 8.27424e-05 | 0.00643151 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94280609 | ACCTACACATTGTGA[A/G]GCTAACCCTGACCTG | 56916 |
rs750830745 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273790 | GAGTGTGTGTAAGGG[A/T]GTGTGTCGGAGGGGT | 56916 |
rs750841433 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241791 | AGCCAGATTAATCTT[G/T]GTGTAGAAAGTCTTA | 56916 |
rs750865987 | in-del | -/ATTAT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255466 | AATTTGAATGTGAAA[-/ATTAT]ATTGTGCCTTTTAAA | 56916 |
rs750869449 | snp | A/G | 0.000507485 | 0.0159212 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94290822 | TATTTATAAATCAAA[A/G]ATTTGTTAATTTTTG | 56916 |
rs750873369 | snp | A/T | 6.03482e-05 | 0.00549276 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208042 | CCCGCTAGGGGGTTA[A/T]ACTGGGGAACGTGCC | 56916 |
rs750893141 | snp | A/C | 4.44998e-05 | 0.00471677 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273606 | TATATATTGTCTTTT[A/C]AACTTTTTAGGGCCT | 56916 |
rs750930113 | in-del | -/TAAT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275402 | AATACTACTTGGTAA[-/TAAT]TGATGTAAATATCTT | 56916 |
rs750940841 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259183 | GCCGGTAGAAGGGTC[A/G]ATATGATGGTGGATG | 56916 |
rs750942735 | in-del | -/CT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236545 | ATGTCTGTCAGTCTC[-/CT]CTTTCCCCTTTCTCT | 56916 |
rs750971735 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235849 | GTAAAAATCTTTCTA[A/G]TTTTGTAATTTTATT | 56916 |
rs751022327 | snp | A/C/G | 5.02713e-05 | 0.00501334 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249789 | AAATTTAATCAGTGT[A/C/G]TACTAAGTGTTTTTA | 56916 |
rs751022535 | snp | G/T | 1.67055e-05 | 0.00289006 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289450 | TTTTTATAAAGCTTT[G/T]AATGCTACTTTCTGA | 56916 |
rs751035082 | snp | C/T | 1.64825e-05 | 0.00287071 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274701 | GTGAACATACCCTAT[C/T]GTAGCAGATGCAAAT | 56916 |
rs751058485 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242065 | TTTTGAGACAGAGTC[-/T]TACTCTGTCCCAGGC | 56916 |
rs751070009 | snp | A/G | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94266170 | TCTCCTAAAAGTGTA[A/G]TTGGAGCTGCTGCTT | 56916 |
rs751089207 | snp | A/C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282760 | ATGAAGTCCTTGATT[A/C/G]ATCAGAAATGTTGTC | 56916 |
rs751120943 | in-del | -/TTG | 0.00760927 | 0.0612106 | utr-variant-3-prime, nc-transcript-variant, cds-indel, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291185 | CTTTTTTTGTTGTTA[-/TTG]TTGTTGTTGTTATAT | 56916 |
rs751159247 | snp | C/T | 1.71728e-05 | 0.00293021 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289618 | TGATGACCATGGGGT[C/T]TATGAACATTTATAA | 56916 |
rs751173646 | in-del | ATATTTAGCAGAGACGGAG/TAT | | | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206800 | CGGCTAATTTTTTGT[ATATTTAGCAGAGACGGAG/TAT]TTTCACCATGTTGGC | 56916 |
rs751210424 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269048 | AAAATTATAAAGACA[A/G]AATTAGAAAAGAATT | 56916 |
rs751236280 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224386 | ACCAGAAATGTTTCT[C/G]ATTTTAGATTTTGGA | 56916 |
rs751333678 | snp | A/G | 0.000135382 | 0.00822634 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289746 | AGCCACAAATATGTA[A/G]TTCTGAAGATGTTGA | 56916 |
rs751372131 | snp | C/T | | | intron-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94253545 | AGTCTCTAACATGTT[C/T]TTGTTGGTTAAGCAA | 56916 |
rs751379806 | snp | A/G | 0.000185891 | 0.00963903 | intron-variant, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94213059 | AGGGATTGAAATAAT[A/G]GCAGGTGAAAGGGAA | 56916 |
rs751395452 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264700 | TATTTTTCTTTTTAT[G/T]CTATAGTTCACAAAG | 56916 |
rs751397934 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225473 | TATAGTCACAAAGAG[C/T]AGGGCCCACACACAT | 56916 |
rs751432817 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244128 | AAAAAGAAAGATTGT[C/G]AAATATTTGGATTCA | 56916 |
rs751445833 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277341 | AATGGGAAAGAAAAT[A/G]GCAATTTCCCTAATC | 56916 |
rs751545270 | in-del | -/T | 1.65573e-05 | 0.00287721 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226306 | TATAGTGTAAGCTGA[-/T]TAATAGATATATTGT | 56916 |
rs751562500 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215036 | TTTGCTTAGTTTTCT[C/G]TATTCCTTGCCCACA | 56916 |
rs751584000 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261702 | GCAACCTCTGACTCC[C/T]GGGCTCAAGCCATCG | 56916 |
rs751592291 | snp | A/G | 1.65042e-05 | 0.0028726 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94236963 | TTAGTTGATTGAATC[A/G]ACAAGCACTATGGAT | 56916 |
rs751594432 | snp | A/G | 1.654e-05 | 0.00287571 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94264869 | ACTGGAAATGGAGGT[A/G]GATGGAACATAGAAC | 56916 |
rs751597058 | snp | C/G | 7.39891e-05 | 0.00608187 | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208232 | GCAGCCATAACAGTC[C/G]TGAGCCACTGGCATG | 56916 |
rs751598740 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262472 | CTTAATAGTTTTTTG[C/T]TCTCAAGCCTTCTTC | 56916 |
rs751635002 | snp | A/C | 1.71123e-05 | 0.00292504 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94240986 | GATGATCAATCTATA[A/C]AAAAGACAAGACTGG | 56916 |
rs751635784 | snp | A/G | 5.06804e-05 | 0.00503365 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94283146 | ATTGATGAGTTTAAT[A/G]CCGATATGGATATCT | 56916 |
rs751651707 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261616 | GTGAAAGATTAAGTT[A/T]GTTTGTTTGTTTTTG | 56916 |
rs751672640 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278368 | GTAATAATACTGTTA[C/T]TGCAATAATTTAAGT | 56916 |
rs751685375 | snp | A/G | | | intron-variant, splice-acceptor-variant | SMARCAD1 | GRCh38.p7 | 4:94213033 | GACTTTTGGGAGTAC[A/G]GTGAGTTTGGAGGGA | 56916 |
rs751690747 | snp | A/G | 3.37132e-05 | 0.00410554 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281609 | GGTATAATTCATGTT[A/G]GTTACAAAAAAATAA | 56916 |
rs751729733 | snp | A/G | 1.65272e-05 | 0.0028746 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94276358 | AACTGTGCGATCAGC[A/G]GTTCTGATGACCGTA | 56916 |
rs751763271 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220992 | TTTCTTTCCCAGAAC[A/G]CCACTGATTCACAAA | 56916 |
rs751799937 | snp | C/T | 1.92317e-05 | 0.00310088 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208288 | AATAAACTGCTGTGG[C/T]ATTGTATCGTATATT | 56916 |
rs751802091 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225666 | GCCAATTACTGAACT[-/A]AATGCTTTACATATA | 56916 |
rs751808178 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227032 | ATGGTTTCTAAAGAG[C/G]GTGGTCAGAAAAGCC | 56916 |
rs751840435 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207720 | CTTTGTTACATAGCA[C/T]TGAGGCTACAAGATC | 56916 |
rs751874295 | snp | A/C | 2.00343e-05 | 0.00316492 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252725 | AAAACAGAAATTTTC[A/C]ATGAAAGCACAAAAT | 56916 |
rs751885495 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240463 | GTGTGAAAAGTAAAT[C/G]AAACAATAGTTTATA | 56916 |
rs751919184 | snp | A/C | | | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208912 | ATAAACTTTGAGGCT[A/C]TTTGGGCAGACATTT | 56916 |
rs751927276 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238953 | ACAACCTCTGCCGTC[A/G]TAAGAGTTTACAATC | 56916 |
rs751947953 | snp | C/T | 0.000177069 | 0.00940762 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290745 | ATACATCAGTTTCTT[C/T]GTATAACTTGTGAGT | 56916 |
rs751980941 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250146 | GTGTCTTAATATTTT[A/G]TAAGCTTTCTACTAC | 56916 |
rs752062564 | snp | A/G | 1.67321e-05 | 0.00289236 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94278963 | CAATGTCATGATGCA[A/G]TTGAGGAAAATGGCC | 56916 |
rs752087254 | in-del | -/AAAAT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219182 | GAAGGAACTGCCTTG[-/AAAAT]CAGTTGCCATCTAAA | 56916 |
rs752134301 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228327 | TTCCCACAATTGCAT[C/T]ATCACTCTTCGTAAA | 56916 |
rs752144743 | snp | A/G | 3.31274e-05 | 0.00406972 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226313 | TAAGCTGATTAATAG[A/G]TATATTGTATTTGCA | 56916 |
rs752174439 | snp | A/T | 0.00013318 | 0.00815919 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280589 | GTTTTGTTTTGTTTT[A/T]AGGAACCTACACATT | 56916 |
rs752223566 | snp | C/T | | | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94251887 | GACGGAGTCTTGCTC[C/T]GTCGCCCAGGCTGGA | 56916 |
rs752265423 | in-del | -/C | | | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291606 | TATAACTGTTTGGGA[-/C]CCCCCATAGAGTTTT | 56916 |
rs752296810 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216241 | GTCACCTCCTAATAC[C/T]ATTACCATAATGGTT | 56916 |
rs752325048 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234528 | GCAGTACTAAGGACA[A/G]TCCATAACTAAGGAT | 56916 |
rs752327646 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224471 | TGATCTGTATTTCAC[A/G]TACACCAAGTTTGTG | 56916 |
rs752346175 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280207 | ATTATTTTAAACTTA[C/T]GGAGAATTTCAAACA | 56916 |
rs752372963 | snp | C/G | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208515 | ATTTCTCTTAGTGCT[C/G]AAGAGGAGAATGCTG | 56916 |
rs752393807 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281796 | GAGGCTGATGCGGGC[A/G]GATTGGTTGGGCTCA | 56916 |
rs752426053 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217234 | GTGATATCGTTTTCT[C/G]CTTTGTTCATTATTC | 56916 |
rs752435227 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224234 | AAAAGTATGATTTGC[C/T]TTTTGCTGTTGTTCC | 56916 |
rs752441151 | snp | A/G | 2.03328e-05 | 0.00318842 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273754 | GTATTTAACTTTATC[A/G]TGTTTTATATAGGTA | 56916 |
rs752483260 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241774 | GCACTGACCGTAACA[A/G]TAGCCAGATTAATCT | 56916 |
rs752483582 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210147 | TTATTTCTTTCTAAT[A/G]ATAACACTCATTTTC | 56916 |
rs752501371 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268769 | TGCAGATAATTAATA[C/T]TTCCTATTTTTAATA | 56916 |
rs752524410 | snp | A/G | 3.37035e-05 | 0.00410495 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94253045 | CCCTTGTATGTGTGT[A/G]TGTATTTAATTCACA | 56916 |
rs752538186 | snp | A/G | 1.65002e-05 | 0.00287225 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289593 | GGTGCACTCAAGGAC[A/G]TTTACATTATGATGA | 56916 |
rs752546459 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241923 | TCACAAAATGGATGA[A/T]CTTGTATACCTGATC | 56916 |
rs752564295 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290382 | TAGTAGTTTATTACT[G/T]CCACATCTCCATGCA | 56916 |
rs752567514 | snp | C/T | 1.64961e-05 | 0.00287189 | missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208422 | AACCTGGACCGTTTT[C/T]GCTTTGAGAAAAGGA | 56916 |
rs752578188 | in-del | -/T | 3.53348e-05 | 0.00420311 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264679 | CCTAGATCTGAACTA[-/T]TCAATTATTTTTCTT | 56916 |
rs752592978 | snp | A/G | 1.71466e-05 | 0.00292797 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289426 | GACAATTTTTTTTTA[A/G]GTAAAATATTTTTAT | 56916 |
rs752611866 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211812 | CAGATGCTTTGTTTC[A/G]TTAAATCTCAGTAAA | 56916 |
rs752636936 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239018 | TATTCCATTGTACTT[C/T]AGATTATTTCAATTA | 56916 |
rs752641765 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94263568 | ATAAATATGGAAAAT[A/G]TATATTGCTATAAAC | 56916 |
rs752684487 | in-del | -/TAG | 1.64741e-05 | 0.00286998 | cds-indel, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94277114 | TATGCCACACATGTT[-/TAG]TAGTAGCACCAGTGA | 56916 |
rs752800094 | snp | A/T | 4.94523e-05 | 0.00497229 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94281543 | TCTATTAAAACATCA[A/T]CAGCATAGGTACCTC | 56916 |
rs752801075 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276203 | TATTTGAGTATCACC[C/T]GTGTCTAGTGCTGTG | 56916 |
rs752808578 | snp | C/T | 1.65293e-05 | 0.00287479 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236944 | TTAATCTTTTCTCGT[C/T]CTGTTAGTTGATTGA | 56916 |
rs752819449 | snp | C/T | 0.000186794 | 0.0096624 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291267 | CTATTATGTCTTGGG[C/T]TTAATAAAAATATTT | 56916 |
rs752823058 | snp | C/T | 1.689e-05 | 0.00290598 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264688 | GAACTATTCAATTAT[C/T]TTTCTTTTTATGCTA | 56916 |
rs752833052 | in-del | -/TG | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210373 | GAGAATCTTGAAAAC[-/TG]AGAAGTTTAGATTTT | 56916 |
rs752851306 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261455 | TGTTTCTGGCACATA[C/T]CTTCAAAGCATAACT | 56916 |
rs752868141 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233524 | TTTAGCAGTTAGATC[C/G]TGATCACACCTAGGT | 56916 |
rs752875045 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260017 | GGTCTTTTAATCTGT[A/G]GATTCCTCATCCCTC | 56916 |
rs752956662 | snp | A/G | | | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94277119 | CACACATGTTTAGTA[A/G]TAGCACCAGTGAAAT | 56916 |
rs752981361 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286340 | AAACCTTCAGTTTTA[C/T]ACATTTGGAGCAAAT | 56916 |
rs753012478 | snp | A/G | 1.65828e-05 | 0.00287943 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94274935 | TTAACATTCATAGTA[A/G]ATATGAAGATTACAA | 56916 |
rs753016554 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248442 | TCAGCTGGTTGTTGT[C/T]CATCTGTGAGCTTTA | 56916 |
rs753071278 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237621 | ATGTCATTCTCAACT[G/T]TTTTCCTGCTTATAT | 56916 |
rs753079394 | snp | A/G | 3.41594e-05 | 0.00413262 | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208226 | TGAAGCGCAGCCATA[A/G]CAGTCCTGAGCCACT | 56916 |
rs753092731 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249118 | ATTAATTAATCTGTT[C/T]GGTTTATACATTATT | 56916 |
rs753094458 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274606 | ACAGGCATGAGCCAC[C/G]TTGCTGGGCCAGTAT | 56916 |
rs753097057 | snp | C/T | 6.6246e-05 | 0.00575488 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94276342 | TTTTGGTGACAGATA[C/T]AACTGTGCGATCAGC | 56916 |
rs753100307 | snp | A/G | 0.000102569 | 0.0071606 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252584 | ATTTATGTATTTCTA[A/G]TTTAGTTACTGTTTT | 56916 |
rs753103528 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219757 | CCTCCTGTTCATTTA[A/G]CATTTTGTGTATTCT | 56916 |
rs753105461 | snp | A/G | | | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206115 | AGTATATATTCTTAA[A/G]CTAACATTTCCATCA | 56916 |
rs753179056 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233234 | TGATCTCTATAACTT[-/A]ACATTCATTTGTTAC | 56916 |
rs753232771 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238661 | TCCTGAAAAATGATA[C/T]GCTCAGTGAACATTT | 56916 |
rs753297281 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285861 | TACTAGGCTTTGTGT[A/G]CATGTGGCAACTTGC | 56916 |
rs753306934 | snp | C/T | 0.000162404 | 0.00900974 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290380 | AATAGTAGTTTATTA[C/T]TGCCACATCTCCATG | 56916 |
rs753335880 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222827 | AAATTAGCCGGGTGT[C/T]GGGGCAGGCACCTGT | 56916 |
rs753340589 | snp | A/T | 1.65296e-05 | 0.00287481 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226285 | ATTCAACAAAGATAC[A/T]GTGATTATAGTGTAA | 56916 |
rs753345463 | snp | A/G | 1.74576e-05 | 0.00295441 | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94278911 | TTTATTTTTTACTGT[A/G]TTCTCTTTGAGTCAC | 56916 |
rs753363574 | snp | A/T | 1.65564e-05 | 0.00287714 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94278684 | GGAGAAGCAGGAGCA[A/T]CTCTATTTGGGTCTT | 56916 |
rs753363649 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255321 | TTCATTAAAAAATGC[A/G]TACTTGAGCCCGTGA | 56916 |
rs753395659 | in-del | -/ATT | 1.66181e-05 | 0.00288249 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278587 | CTCTTTACTAGAATG[-/ATT]ATCTTAAACTGTTTT | 56916 |
rs753401867 | in-del | -/GA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285723 | TTCTTGCGTAGCATT[-/GA]TATTTCAGGGTGCTG | 56916 |
rs753428627 | snp | A/T | 1.65151e-05 | 0.00287355 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226206 | GAATACAGTATATTG[A/T]TTTGTCTTCTGATAG | 56916 |
rs753443144 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248835 | TTTCTATCTAAGGTA[C/T]TGAAAGAGAAAAATA | 56916 |
rs753463302 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226984 | GCTGGGATTACAGGC[A/G]TTAGACACCACACCT | 56916 |
rs753551232 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274414 | CACCGCAACCTCCGC[C/T]TCCCAGGTTCTCGTG | 56916 |
rs753559101 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238528 | TCTTCCTCATTATTT[C/T]GTCCCTAGCACTTAC | 56916 |
rs753559198 | snp | C/G | 1.65323e-05 | 0.00287505 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94249655 | TTTCTCCCCATTAGG[C/G]AGAGGAATCAAATGA | 56916 |
rs753562150 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216103 | TATTCCTAGACCACA[A/G]TCTTTTAACCCCATG | 56916 |
rs753598840 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221674 | TTGTGGCTTGGATAT[A/G]TAGTTTTCATGAAGA | 56916 |
rs753611318 | snp | C/T | 6.78162e-05 | 0.00582267 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208314 | ATATTGTTTTCATGG[C/T]CTTTTTTCCTCTCTT | 56916 |
rs753631982 | snp | C/G | 3.57596e-05 | 0.0042283 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273579 | ATTTATTTTTTGTTT[C/G]TTTTAAAATGTTATA | 56916 |
rs753672200 | in-del | -/TTATTG | 3.52675e-05 | 0.00419911 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281636 | ATAACTCATTTATTA[-/TTATTG]TTAGGATTTTAATTG | 56916 |
rs753672393 | snp | A/G | 1.88478e-05 | 0.00306978 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276520 | TACTGTAAAATTTAG[A/G]TTACGTAATTTAATA | 56916 |
rs753679290 | snp | C/T | 1.72347e-05 | 0.00293548 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284934 | ATATTTAGTAACCAA[C/T]GGACATATTTTGTAT | 56916 |
rs753699973 | snp | A/G | 1.99039e-05 | 0.00315461 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241044 | GTATCAAAATTGGCT[A/G]CTTAAGGTTAGGATA | 56916 |
rs753711269 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250320 | GCACTGATTTATTTG[A/C]GTATATATGTTCAGA | 56916 |
rs753739657 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222811 | CTACAAAAAAATACA[A/G]AAATTAGCCGGGTGT | 56916 |
rs753768828 | snp | C/T | 3.31406e-05 | 0.00407053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285086 | TGAGTTGTTTGTAAG[C/T]AGAAACTTCAATATT | 56916 |
rs753776152 | in-del | -/GGA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288659 | TATTTGTGAGAGAGG[-/GGA]GGAGGAGAGAAGTGG | 56916 |
rs753875104 | snp | A/G | | | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94240949 | TTCTTCTTCAGAGCC[A/G]TATGAGGAAGATGAA | 56916 |
rs753911603 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241839 | CACAGACTCAAGCCC[A/T]GTTGCCATGGCCATT | 56916 |
rs753935390 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288504 | GAAGCAAGGATGTCA[C/G]TGAACTGACATCCCT | 56916 |
rs753938349 | snp | A/G | 0.000325945 | 0.0127619 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94290888 | GATGCTAGGTAGTAC[A/G]ACCCTCTGGATTTGG | 56916 |
rs753950026 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211586 | GCTTACAGGACAGAA[A/G]TTGTATGTAGTCAAA | 56916 |
rs753959162 | snp | A/G | | | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94251921 | CAGTGGCACAGTCTC[A/G]GCTAACTGCAACCTC | 56916 |
rs753959232 | snp | A/G | 3.29489e-05 | 0.00405874 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94277055 | CTCACAGGCACACCT[A/G]TACAGAACAATCTGT | 56916 |
rs753964296 | in-del | -/AA | 1.67209e-05 | 0.00289139 | splice-acceptor-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208345 | ATTTTTCCCCTGCAG[-/AA]ATAGTTCATTTAAAG | 56916 |
rs754007653 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210039 | GAAAGCAGTTTGTAA[A/G]CTGGATTTCAGTGGA | 56916 |
rs754050277 | snp | G/T | 3.29576e-05 | 0.00405928 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264672 | TCTCTTTCCTAGATC[G/T]GAACTATTCAATTAT | 56916 |
rs754100136 | snp | G/T | 1.65463e-05 | 0.00287626 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94234012 | ATGGCACGTAGAAAT[G/T]ATGATATTTCAGAAC | 56916 |
rs754127131 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273949 | TTTAAAATTTTAGAC[C/G]AAGGACGATTTATGT | 56916 |
rs754165766 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212497 | ATTTATTTATTATTA[-/T]TTTTTTTGAGATGGA | 56916 |
rs754192844 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261336 | CTGTTATTTATCACT[A/G]AACTCATAATATGCT | 56916 |
rs754196866 | snp | A/G | 8.2411e-05 | 0.00641862 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94281517 | ACCATGATGCTGGAT[A/G]TCTTAGAGGTTCTAT | 56916 |
rs754225045 | snp | A/G | 4.97492e-05 | 0.0049872 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236928 | GTGCTGATTTAAAAC[A/G]TTAATCTTTTCTCGT | 56916 |
rs754252752 | snp | A/G | 1.64803e-05 | 0.00287052 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274729 | AATAATGTCTCTTCT[A/G]TTCCATAGATAACTG | 56916 |
rs754267606 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230755 | CAGTAGATAAAATCT[C/G]CTAGGAAGCATTCAT | 56916 |
rs754275482 | snp | A/G | 1.65425e-05 | 0.00287593 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280792 | GAAGGTATTAAAAAA[A/G]AATGGCGTTTCTTTT | 56916 |
rs754285618 | in-del | -/AAT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273521 | GGGAAATCAAAAGTG[-/AAT]ACAGCACAGAATTAC | 56916 |
rs754298038 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272078 | TCTCCTGAGTCCTCT[A/C]TTTGACTTGAAGACA | 56916 |
rs754363218 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248284 | CTTTTTTATGACTTA[C/G]TGATATTCCATTTTA | 56916 |
rs754417571 | snp | A/C | 1.67725e-05 | 0.00289585 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249794 | TAATCAGTGTGTACT[A/C]AGTGTTTTTATTATA | 56916 |
rs754423097 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288800 | CTAGTAAATTAATCA[A/G]CTCATCTCAAAATAT | 56916 |
rs754448929 | snp | C/T | 1.65135e-05 | 0.00287341 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274847 | ATTAAAAATAAAGTA[C/T]AGCACAATAAATAGT | 56916 |
rs754459773 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244526 | TTCTAGGATTTAAGG[C/T]TCCTAAAGGTAACAT | 56916 |
rs754522294 | snp | G/T | 2.06879e-05 | 0.00321613 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241052 | ATTGGCTGCTTAAGG[G/T]TAGGATATGTGGAGT | 56916 |
rs754523111 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235881 | AAAAATAAGATTGAT[-/A]ATGCATAATTTCCCT | 56916 |
rs754525664 | snp | A/G | 1.78637e-05 | 0.00298857 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264909 | TTCTAAACCAAAGGT[A/G]ATCTTTGTTGAATAT | 56916 |
rs754527654 | snp | A/G | 1.68744e-05 | 0.00290463 | missense, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94278947 | AAAACACAGAAATGT[A/G]CAATGTCATGATGCA | 56916 |
rs754528405 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233465 | TGCTGAGGAAATGTT[G/T]TGTTTCTGGCAGAGA | 56916 |
rs754543276 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214589 | GTTAACCAAGGACAA[A/G]AAGCTAGTGGAGAGG | 56916 |
rs754647071 | in-del | -/T | | | upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207685 | CCCCACGCTAGGAAA[-/T]TTTTTTTTTTATTTT | 56916 |
rs754695779 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247646 | GCTGTCATCACCTCG[-/T]TAATAGCATGCTATA | 56916 |
rs754696373 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247184 | ATAATAGTAGCCCAT[A/G]CATCATGGGTCAGGG | 56916 |
rs754697669 | in-del | -/A | 0.00012453 | 0.00788982 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252759 | TTTAACAAGAAACGT[-/A]AAAAAAATGTTTTTA | 56916 |
rs754757048 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221737 | CCCGTTTAGCTCTTA[C/T]ATGGGCTCTTTTGGC | 56916 |
rs754761693 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213447 | GGAGGTTTTAGACAA[C/T]ATAGATGAAACTGAA | 56916 |
rs754795964 | snp | C/T | 3.38226e-05 | 0.0041122 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208320 | TTTTCATGGCCTTTT[C/T]TCCTCTCTTTATTTT | 56916 |
rs754868411 | snp | A/G | 1.65162e-05 | 0.00287365 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94249662 | CCATTAGGGAGAGGA[A/G]TCAAATGAGTCTGCA | 56916 |
rs754869021 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288601 | ACAGAGAAAAGAAGA[A/G]TGGATGAAAGTACTC | 56916 |
rs754874610 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241092 | TTATTAGACCTGAAA[A/G]TCCACCTAAATGAAT | 56916 |
rs754876205 | snp | A/G | 5.10252e-05 | 0.00505074 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284939 | TAGTAACCAATGGAC[A/G]TATTTTGTATTTTTT | 56916 |
rs754889337 | snp | C/T | 3.29554e-05 | 0.00405914 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252881 | GATGGAGGATGGCTA[C/T]AAAGGTAAAATTCTT | 56916 |
rs754893890 | in-del | -/TTCCTCTTTGATT | 1.64781e-05 | 0.00287033 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226322 | AATAGATATATTGTA[-/TTCCTCTTTGATT]TTTGCATGTGTGTGA | 56916 |
rs754898168 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261056 | AATGACAGATTAGAT[A/C]ACAATATGCTAATTT | 56916 |
rs754934972 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210067 | GGAATGTTTTAGTTA[C/T]TTATCAGTATTGGTC | 56916 |
rs754954648 | snp | A/T | 0.000325998 | 0.012763 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94290889 | ATGCTAGGTAGTACG[A/T]CCCTCTGGATTTGGA | 56916 |
rs754976130 | snp | C/T | 0.000117112 | 0.00765129 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276524 | GTAAAATTTAGATTA[C/T]GTAATTTAATATATG | 56916 |
rs754987434 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274346 | TTATTTATTTTTTTT[A/G]AGACAGTCTCGCTGT | 56916 |
rs755012136 | snp | A/G | | | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209214 | ATTGAACAGTTAACT[A/G]TTAGAGGAATATATT | 56916 |
rs755023710 | in-del | -/TGTA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281049 | TCATAGGTGACAATC[-/TGTA]TGTGTGCTTCAAAAT | 56916 |
rs755029636 | snp | A/G | 1.65968e-05 | 0.00288065 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94234029 | TGATATTTCAGAACT[A/G]GAAGACCTTTCGGAA | 56916 |
rs755034134 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241844 | ACTCAAGCCCAGTTG[C/T]CATGGCCATTTGTAA | 56916 |
rs755077085 | in-del | -/TG | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220674 | CCTTTTTCACGATAT[-/TG]ATATTTGCACTCATG | 56916 |
rs755083034 | snp | C/T | 1.67973e-05 | 0.00289799 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94253031 | TTATTCTTTTTTTCC[C/T]CTTGTATGTGTGTGT | 56916 |
rs755117543 | snp | C/G/T | 3.57604e-05 | 0.00422838 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233930 | CATTAAAAATGTTTT[C/G/T]TGCTCCTCTAAAAAT | 56916 |
rs755123865 | snp | C/T | 1.65553e-05 | 0.00287705 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236935 | TTTAAAACATTAATC[C/T]TTTCTCGTTCTGTTA | 56916 |
rs755146739 | snp | A/C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255827 | TTTAAATATTGTTTT[A/C/T]AAATTTTTCTTCATA | 56916 |
rs755164795 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258608 | TTCTGAATTCAGTGC[A/T]TGCCACTTTTTTTAT | 56916 |
rs755185457 | snp | C/T | 0.000148384 | 0.0086122 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94280657 | AGTTATGACAGACTT[C/T]GAACTACATGTACTT | 56916 |
rs755233797 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229852 | TGATAATTCTAATCT[A/G]TCACTACAGGTCTTT | 56916 |
rs755258196 | snp | G/T | 0.000183301 | 0.00957168 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291202 | GTTGTTGTTGTTATA[G/T]CCATACTTTTATCTC | 56916 |
rs755298216 | in-del | -/CT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284439 | TGAGACAGAGCCTCA[-/CT]CTGGCTGGAGTGCAG | 56916 |
rs755338206 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218976 | ACCACCACGCCTGGC[C/T]AATTTTTGTGTTTTT | 56916 |
rs755368046 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247649 | TGTCATCACCTCGTA[A/C]TAGCATGCTATACCC | 56916 |
rs755375373 | snp | A/C | 1.65252e-05 | 0.00287443 | missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208579 | CAGATATAACTGAAA[A/C]AACAGGTGAGTTACA | 56916 |
rs755393309 | snp | A/G | 0.000452386 | 0.0150329 | splice-donor-variant, intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208071 | CCTGCGCGTGCTTGG[A/G]TAAGAGGAGGTTGCA | 56916 |
rs755426206 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269331 | GGAGATTAAGGGGAC[A/G]GGATAAAAGCTGGAG | 56916 |
rs755435179 | in-del | -/TTTC | 0.00021634 | 0.0103982 | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94279057 | TGCTAAAGGTAAGGA[-/TTTC]TTTCATATTATGTTA | 56916 |
rs755441898 | in-del | -/AA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257687 | GTTCTCCGCCCCCAC[-/AA]AAAAAAATCTATATC | 56916 |
rs755446647 | snp | A/G | 5.04388e-05 | 0.00502164 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289651 | TTTTATAATTTCCAT[A/G]TTACATTTCTCATAG | 56916 |
rs755480105 | snp | C/G/T | 3.60863e-05 | 0.0042476 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250884 | CATTATAGTCTGTAT[C/G/T]TTAGTATATAAGAAA | 56916 |
rs755524485 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272166 | ATTTCTTCTTACAAG[A/G]ACAGTCATATTGGGT | 56916 |
rs755536894 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233281 | TCTAGAGTGCCTACC[A/G]TGTTTGAAAACCAAA | 56916 |
rs755567109 | snp | A/T | 1.65356e-05 | 0.00287533 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274872 | AATAGTCATGTGTTT[A/T]TTGTTTTTAAATTCT | 56916 |
rs755569121 | snp | A/T | 1.70397e-05 | 0.00291883 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250713 | CTGCAAGTTGCTAAT[A/T]TGAGATTTTTAACAA | 56916 |
rs755589661 | in-del | -/ATT | 1.91272e-05 | 0.00309245 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233905 | CTATAATGAAATAAC[-/ATT]AGTAATACATTAAAA | 56916 |
rs755601581 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271003 | CACTCCTCCCCAAGA[C/T]GAAGATAGATTTATT | 56916 |
rs755606670 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248338 | GACGCACATTTGATA[C/T]ATTAACAAATGAACA | 56916 |
rs755651682 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244471 | TATCTGTTATGAACG[C/G]ATGCCTCGAATAACC | 56916 |
rs755665740 | snp | C/G | 1.66624e-05 | 0.00288633 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94264891 | ACATAGAACAACCTT[C/G]CATTCTAAACCAAAG | 56916 |
rs755677104 | snp | A/G | 0.000153645 | 0.0087635 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289817 | TGGTGATTGTTTGTA[A/G]CAAATATGCTAATGC | 56916 |
rs755681485 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225751 | GAGGAGGAAATTAAG[G/T]CTTAGAGAAATTAAT | 56916 |
rs755783073 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277535 | AAACTAGACAAAGCT[A/G]GAATATCCAGAAAAT | 56916 |
rs755795846 | snp | A/G | 1.65578e-05 | 0.00287726 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94278670 | TTGTGTGCAATGTCG[A/G]AGAAGCAGGAGCAAC | 56916 |
rs755836323 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255056 | GTACCTCTAAACAAC[A/T]TCAAAAGGAAACAAA | 56916 |
rs755838853 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213449 | AGGTTTTAGACAATA[G/T]AGATGAAACTGAAAA | 56916 |
rs755918510 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233916 | TAACATTAGTAATAC[A/G]TTAAAAATGTTTTTT | 56916 |
rs755933863 | snp | A/G | 3.31049e-05 | 0.00406834 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237064 | ATTTATTGTTACGTC[A/G]TAATAATAGTACCTT | 56916 |
rs755947017 | snp | C/T | | | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94279220 | CAGGCAGTCTGGGCT[C/T]ACTGCAACTTCTGCC | 56916 |
rs755954811 | snp | A/C/T | 0.000159293 | 0.00892332 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208246 | CCTGAGCCACTGGCA[A/C/T]GTTTGCGGGCCCTTT | 56916 |
rs755982968 | snp | A/G | 1.75628e-05 | 0.00296329 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284928 | ATAACTATATTTAGT[A/G]ACCAATGGACATATT | 56916 |
rs756001597 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258286 | CACCCTCCTGAGTAG[C/T]TGGGATTACAGGCGT | 56916 |
rs756007376 | snp | A/G | 3.3036e-05 | 0.0040641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270693 | AACTGATAGAAATAT[A/G]GATGTGTAATATTTG | 56916 |
rs756033140 | snp | C/T | 1.64841e-05 | 0.00287085 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94276372 | CAGTTCTGATGACCG[C/T]AGTCTGTTTCGACGG | 56916 |
rs756041278 | in-del | -/TTT/TTTT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282099 | CAAATACGTTTTTTT[-/TTT/TTTT]GTTTTTTTTTTTTTT | 56916 |
rs756070300 | in-del | -/AT | 5.13765e-05 | 0.0050681 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278401 | ATAATTCCTAAAAGG[-/AT]ATGTTTTTATTTTGC | 56916 |
rs756080743 | snp | A/G | 3.39645e-05 | 0.00412081 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208310 | TCGTATATTGTTTTC[A/G]TGGCCTTTTTTCCTC | 56916 |
rs756107229 | snp | G/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208030 | GCGGGCGCGAGGCCC[G/T]CTAGGGGGTTATACT | 56916 |
rs756107379 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221642 | ATAAAACAGTGTCAT[C/T]TGACTAAATAAATTA | 56916 |
rs756107825 | snp | A/G | 0.000116909 | 0.00764467 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94283156 | TTAATACCGATATGG[A/G]TATCTTTGTGTTTCT | 56916 |
rs756113804 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233089 | ATAACATGAGTACAT[A/G]TAGAGAAATTGCATA | 56916 |
rs756130701 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287522 | CCTTAGTTGTTACCA[G/T]AGTACCAGCAGCAGG | 56916 |
rs756140707 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262728 | AGGTCTTAGATTTTA[C/T]TAGTCTTTTTGTGAT | 56916 |
rs756229280 | snp | A/C/T | 1.83085e-05 | 0.00302554 | missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252749 | ACAAAATGGCTTTAA[A/C/T]AAGAAACGTAAAAAA | 56916 |
rs756243533 | in-del | -/TTTC | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233585 | ATTTAATCTTCATAA[-/TTTC]TTAGGAGTAGCATAA | 56916 |
rs756266265 | snp | A/G | 4.99713e-05 | 0.00499831 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226346 | TGTGTGAGATTTTCC[A/G]AGAAAAAAACCTACC | 56916 |
rs756290163 | in-del | -/AG | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281350 | GAAGCAGTTTATCAC[-/AG]AGAATTTTCTGCAAA | 56916 |
rs756317492 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228461 | AACCCAGAAATACCA[A/G]TTAACACTAGTACAG | 56916 |
rs756352035 | snp | A/G | 6.59272e-05 | 0.00574101 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252842 | TAGTTCACTAGATGA[A/G]GACTATAGTAGTGGT | 56916 |
rs756354460 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257235 | ATTTTTTGAGAATGA[C/T]TTGTTTTACCTAAAA | 56916 |
rs756372344 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240779 | ATATGTAGAACAACA[A/G]ACACTGGGCCTGATA | 56916 |
rs756373817 | in-del | -/A | 1.6486e-05 | 0.00287102 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289534 | ATCAATGGGCCTGTG[-/A]AATAAGAACTGTGAA | 56916 |
rs756375130 | snp | C/T | 0.000167827 | 0.00915891 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94290828 | TAAATCAAAGATTTG[C/T]TAATTTTTGGAAATC | 56916 |
rs756379712 | in-del | -/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284825 | ATGTCAGTCTCAAGT[-/G]GCTTAAATAAAAGAA | 56916 |
rs756499220 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229710 | TAGGAATTAATGTCA[C/T]TGCCCTTTCAGCAGA | 56916 |
rs756512246 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258576 | TCCTTTTGTCTCTCT[C/T]ATTTTGAGTCTCTTG | 56916 |
rs756518960 | snp | A/C | 1.65007e-05 | 0.00287229 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94249679 | CAAATGAGTCTGCAG[A/C]ATCTAGCAGTAATTG | 56916 |
rs756525251 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234603 | CAGAAACAAAGGAGT[A/G]TAGTTGAAATGTAAA | 56916 |
rs756580860 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230909 | AGTAATGTTGCAGAA[C/G]CCCTGAGGTGAGGGT | 56916 |
rs756609271 | snp | A/T | 2.05636e-05 | 0.00320646 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273610 | TATTGTCTTTTAAAC[A/T]TTTTAGGGCCTAGGA | 56916 |
rs756646470 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227735 | ATTGAGAACACTCCT[A/G]GACGTCTAAATGGAG | 56916 |
rs756649552 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247098 | TATCTGCAGTTCCTT[A/T]AGGACTGTAGTAATT | 56916 |
rs756665700 | in-del | -/A | 3.32231e-05 | 0.00407559 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278594 | TAGAATGATTATCTT[-/A]AAACTGTTTTTTCTG | 56916 |
rs756693746 | snp | A/G | 0.00011553 | 0.00759944 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94280773 | TCTTGTCTGAATTGA[A/G]ACAGAAGGTATTAAA | 56916 |
rs756733762 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283677 | AAAAATACAAAAAAT[C/T]AGCCGGGCATGGTGG | 56916 |
rs756740141 | snp | A/G | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208551 | GAAGTTAGCAGGGCA[A/G]ACACTCCTGATTCAG | 56916 |
rs756823408 | snp | G/T | 0.00149198 | 0.027272 | intron-variant, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94213065 | TGAAATAATGGCAGG[G/T]GAAAGGGAAGAGAGA | 56916 |
rs756833494 | in-del | -/AT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287991 | TCCATCTCTATTAAA[-/AT]ATATATATATATTTT | 56916 |
rs756843897 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225480 | ACAAAGAGTAGGGCC[C/G]ACACACATGACCTCA | 56916 |
rs756845824 | snp | C/T | 1.68789e-05 | 0.00290503 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278410 | AAAAGGATATGTTTT[C/T]ATTTTGCTCAGAAAT | 56916 |
rs756890814 | snp | C/G/T | 3.83931e-05 | 0.00438125 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289628 | GGGGTTTATGAACAT[C/G/T]TATAACTTTTTATAA | 56916 |
rs756899482 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212431 | CCACGTGCCTTGGCC[G/T]CTGAAAGTGCTAGGA | 56916 |
rs756925605 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269094 | AGAAATACTGCTTTT[A/T]CTCCTACCTATACTT | 56916 |
rs756930657 | in-del | -/TCTC | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266307 | ATCACTTTAAAAATT[-/TCTC]TCTCAAAACCACATT | 56916 |
rs756932532 | in-del | -/TGTTTTAAAATGTTATATATTG | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273577 | TATTTATTTTTTGTT[-/TGTTTTAAAATGTTATATATTG]TGTTTTAAAATGTTA | 56916 |
rs756985664 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224400 | TCATTTTAGATTTTG[G/T]AATATTTGCATATAC | 56916 |
rs757000032 | snp | A/G | | | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252550 | ATGTTTTAAGTTTTT[A/G]TTTGAAGTCTATCTT | 56916 |
rs757045624 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286374 | TGGCTCTCTTGGGCA[A/G]GCTTTAGACATCTTA | 56916 |
rs757048833 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213291 | GGATCACAAAAAGTC[A/G]CAGAGATATGACCTT | 56916 |
rs757147249 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269090 | AATTAGAAATACTGC[-/T]TTTTCTCCTACCTAT | 56916 |
rs757158768 | snp | A/G | 1.69945e-05 | 0.00291496 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281616 | TTCATGTTAGTTACA[A/G]AAAAATAACTCATTT | 56916 |
rs757169115 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219808 | TATAACATAGTTACT[C/T]ATGAACATGGCTACT | 56916 |
rs757186145 | in-del | -/AAAT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288892 | GATTTAGAAAATCTC[-/AAAT]AATTCCTGTAAGTGC | 56916 |
rs757196429 | snp | C/T | 1.65312e-05 | 0.00287495 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237051 | TTAAGCCATGTCGAT[C/T]TATTGTTACGTCATA | 56916 |
rs757206848 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219361 | AGTATTTCTATGTGA[A/T]TTCATAATCTCCCAC | 56916 |
rs757221493 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277368 | AATCAATGGCCAGAA[A/G]TCTTGGTTAATATCC | 56916 |
rs757236219 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207851 | ATCAGCTTCCTCTCA[A/G]CTGGGATCGCGCCGC | 56916 |
rs757279940 | snp | A/G | 1.6504e-05 | 0.00287258 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94236964 | TAGTTGATTGAATCA[A/G]CAAGCACTATGGATG | 56916 |
rs757284178 | snp | A/G | 1.65842e-05 | 0.00287955 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94264883 | TGGATGGAACATAGA[A/G]CAACCTTCCATTCTA | 56916 |
rs757291147 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219881 | TTATTTTGCTTTAAT[A/G]TCCCCCACCTGGTAC | 56916 |
rs757293998 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262534 | GAACTCTCTAAAACC[C/T]TTCAATAGCTTTTTA | 56916 |
rs757302727 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244311 | AGTTTCCTACAAACA[A/G]TGCTACAGTTTCCTA | 56916 |
rs757343363 | snp | A/G | 6.74059e-05 | 0.00580503 | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208236 | CCATAACAGTCCTGA[A/G]CCACTGGCATGTTTG | 56916 |
rs757373165 | snp | C/G | 1.66214e-05 | 0.00288278 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94274960 | TTACAATGTAATTGT[C/G]ACCACGTAAGTATTG | 56916 |
rs757387317 | snp | C/T | 1.68425e-05 | 0.00290189 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94283148 | TGATGAGTTTAATAC[C/T]GATATGGATATCTTT | 56916 |
rs757470655 | snp | C/G | | | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208964 | CAAAATATTGATCAT[C/G]TACTGTGAGCTAGAC | 56916 |
rs757488807 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237906 | ATGTTCAAGCAAAGT[A/G]TATGCACATTTTAAA | 56916 |
rs757499753 | snp | C/G | 1.65231e-05 | 0.00287424 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94276362 | GTGCGATCAGCAGTT[C/G]TGATGACCGTAGTCT | 56916 |
rs757515200 | snp | A/G | | | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291745 | GTGACCTTACGTGTG[A/G]TACTTCACAGTCCAT | 56916 |
rs757516627 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271400 | TAGTCCAGGTGTTGT[C/T]ATATGGAAACTTGAC | 56916 |
rs757536260 | snp | A/G | 0.000265045 | 0.0115088 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226317 | CTGATTAATAGATAT[A/G]TTGTATTTGCATGTG | 56916 |
rs757543335 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249577 | TTCAGATCAAGTCAA[A/G]ATACAATGATAATTG | 56916 |
rs757552049 | snp | A/G | 0.000162641 | 0.00901633 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290040 | TTTATTGCTATTTGA[A/G]GCAGATGTTCACCAA | 56916 |
rs757570179 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286083 | CCATAATAGTTGATA[A/C]AATTAACTATAAGTC | 56916 |
rs757627876 | snp | A/G | 1.64876e-05 | 0.00287116 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252825 | TCAGGTTCTGATGTC[A/G]GTAGTTCACTAGATG | 56916 |
rs757672552 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272274 | AGGTTACGACTCCAA[C/T]GTATGTATTGTCAGT | 56916 |
rs757680980 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282170 | AGTGGCGCGATCTCG[G/T]CTCACTGCAAGCTCC | 56916 |
rs757687469 | snp | C/T | 6.58968e-05 | 0.00573969 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94270774 | TTGAATTGGCTGGCA[C/T]TGGTACATAAACATG | 56916 |
rs757704006 | snp | C/T | 4.95127e-05 | 0.00497533 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226231 | TGATAGTGAAGATGT[C/T]GTTTCCCCAAATTGC | 56916 |
rs757705893 | snp | C/T | 1.65894e-05 | 0.00288 | missense, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94278994 | AATCATCCTTTATTA[C/T]ATCGCCAATATTACA | 56916 |
rs757763245 | snp | A/T | 9.97855e-05 | 0.00706277 | splice-acceptor-variant | SMARCAD1 | GRCh38.p7 | 4:94280590 | TTTTGTTTTGTTTTA[A/T]GGAACCTACACATTG | 56916 |
rs757771088 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257122 | GTTTTTAATGAAGAG[A/G]TATGATTGGGGCCAT | 56916 |
rs757891263 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214893 | TAGCACTTGTTGATA[A/T]GTGAGAGACATTTTT | 56916 |
rs757916631 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280376 | GATGTTATTTCATCT[A/G]TAAATATTTTAGTAT | 56916 |
rs757927634 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233671 | GGCATGCAATAAATG[C/T]GTGTGAGTCCTAACA | 56916 |
rs757949606 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246941 | AGCCATATTGATTTG[C/T]TCCAGCAAAAATACC | 56916 |
rs757965766 | snp | A/T | 2.95268e-05 | 0.00384221 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273593 | TGTTTTAAAATGTTA[A/T]ATATTGTCTTTTAAA | 56916 |
rs757976535 | snp | C/T | 1.64917e-05 | 0.00287151 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208427 | GGACCGTTTTCGCTT[C/T]GAGAAAAGGAATAAG | 56916 |
rs758037653 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223115 | ATTAAATTTTTAGAC[A/C]CCCCTACAGGTGAAA | 56916 |
rs758038823 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289395 | AAGAATTCACCAAAG[-/A]AAAAAAAATAATTGA | 56916 |
rs758064572 | snp | A/G | 0.000198046 | 0.00994906 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94249671 | AGAGGAATCAAATGA[A/G]TCTGCAGAATCTAGC | 56916 |
rs758096718 | snp | A/C/G | 4.95711e-05 | 0.0049783 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94284981 | ACTAGTTATAAAACT[A/C/G]ATAAGCCAAGGGACG | 56916 |
rs758110062 | in-del | -/GTT | 1.6489e-05 | 0.00287128 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285074 | AGTAGATGAAGGTGA[-/GTT]GTTTGTAAGCAGAAA | 56916 |
rs758157696 | in-del | -/T | 5.74146e-05 | 0.00535761 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226068 | ATAACTAACAACAGA[-/T]TTCGTTTTCCAGTTG | 56916 |
rs758185100 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288841 | AAATTGAATTAATCA[G/T]GGATGGCTAGATTAT | 56916 |
rs758197444 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224280 | GGAAATAGAGAAATG[C/T]TTGTGTTTTGGTGCT | 56916 |
rs758224250 | in-del | -/CTAA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281658 | TAGGATTTTAATTGT[-/CTAA]CAAACAATTGATAGT | 56916 |
rs758233271 | in-del | -/TTATC | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215773 | TATTGCAGACCTTTA[-/TTATC]TTTAATAAGCTAATA | 56916 |
rs758244473 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208521 | CTTAGTGCTGAAGAG[A/G]AGAATGCTGAAGGGG | 56916 |
rs758296733 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229926 | ACTTCTACCAGTATC[A/G]GTATATTTTACTAAT | 56916 |
rs758297118 | snp | A/G | 1.67184e-05 | 0.00289118 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94234044 | GGAAGACCTTTCGGA[A/G]TTGGAAGACCTTAAA | 56916 |
rs758314184 | snp | A/C | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94277123 | CATGTTTAGTAGTAG[A/C]ACCAGTGAAATACGA | 56916 |
rs758349283 | snp | C/T | 1.68627e-05 | 0.00290363 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264692 | TATTCAATTATTTTT[C/T]TTTTTATGCTATAGT | 56916 |
rs758352631 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265799 | TGAATTATGGTATAT[C/G]CATACTTTGCAATGT | 56916 |
rs758384710 | snp | A/G | 0.000369822 | 0.0135932 | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208090 | GAGGAGGTTGCATGA[A/G]GGTCAGCTCGTGGTT | 56916 |
rs758439358 | snp | A/C | 8.6986e-05 | 0.00659435 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278393 | TTAAGTGAATAATTC[A/C]TAAAAGGATATGTTT | 56916 |
rs758451410 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260077 | TTGGTAAAGAAACTG[G/T]GTCATTTGTTCTATA | 56916 |
rs758462309 | snp | C/G | 1.65787e-05 | 0.00287907 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280808 | AATGGCGTTTCTTTT[C/G]TATTTTCTCAATTAC | 56916 |
rs758468008 | snp | C/T | | | intron-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94253404 | AAATTTTACTACAAC[C/T]ACTTGAAGAGCAATA | 56916 |
rs758468735 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210139 | TTCTGTTTTTATTTC[G/T]TTCTAATGATAACAC | 56916 |
rs758474561 | snp | C/G/T | 3.30449e-05 | 0.00406467 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236947 | ATCTTTTCTCGTTCT[C/G/T]TTAGTTGATTGAATC | 56916 |
rs758476227 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241956 | TAAAAATTTTCTCTG[C/T]CACGTGTGCACCCTT | 56916 |
rs758578259 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248493 | CAGTGTGCCTGGGCT[A/G]TAAAGGTGGCAGTAT | 56916 |
rs758604550 | snp | C/T | 1.702e-05 | 0.00291714 | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208230 | GCGCAGCCATAACAG[C/T]CCTGAGCCACTGGCA | 56916 |
rs758618081 | snp | G/T | | | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206178 | TCAGTGTATCGAAAT[G/T]ATATCTGCATTCTCA | 56916 |
rs758629238 | snp | A/G | 1.65888e-05 | 0.00287996 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94274942 | TCATAGTAGATATGA[A/G]GATTACAATGTAATT | 56916 |
rs758645669 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219788 | CTCATTGCACAAATT[A/G]TGCTTATAACATAGT | 56916 |
rs758676759 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285893 | AGTTTCAGGTTGTCC[A/G]GGAAATACAGTAAAG | 56916 |
rs758687190 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261516 | CTGTGAATAGTTACG[A/T]ATTTAATTACTCAGA | 56916 |
rs758714667 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257793 | CCTCCATATCTTTAT[A/G]TAATATAGTTATAAT | 56916 |
rs758777559 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207652 | GGTGTTTTGGAAGGT[C/T]CCGGCACGGCTACCG | 56916 |
rs758810979 | snp | A/G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237625 | CATTCTCAACTTTTT[A/G/T]CCTGCTTATATACAC | 56916 |
rs758839479 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284016 | ATTTTGACATTGGTC[A/C]CAGCACTGTAAAGAG | 56916 |
rs758848140 | snp | C/T | 2.22388e-05 | 0.0033345 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252698 | CCCTAAAAATGCAAC[C/T]AAAACAAAACTAAAA | 56916 |
rs758870741 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238708 | GCTTGGGAAGTTTTG[C/T]AGCTTCCCAATACAT | 56916 |
rs758871813 | snp | C/G | 1.68821e-05 | 0.0029053 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252589 | TGTATTTCTAATTTA[C/G]TTACTGTTTTTGTCT | 56916 |
rs758889858 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272168 | TTCTTCTTACAAGGA[C/T]AGTCATATTGGGTTC | 56916 |
rs758897655 | snp | A/G/T | 3.31188e-05 | 0.00406921 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94278694 | GAGCAACTCTATTTG[A/G/T]GTCTTTTCAACAGAT | 56916 |
rs758908976 | snp | A/G | 1.65078e-05 | 0.00287291 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226220 | GATTTGTCTTCTGAT[A/G]GTGAAGATGTCGTTT | 56916 |
rs758913542 | snp | A/G | 0.00016243 | 0.00901047 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290387 | GTTTATTACTGCCAC[A/G]TCTCCATGCATCAGC | 56916 |
rs758962775 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227005 | CACCACACCTGGCTC[A/G]AGGGTCAGGGAATGG | 56916 |
rs758974637 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241374 | TGCCCTCTTCATTAC[A/G]TTGGGTTCTCTGAAC | 56916 |
rs758992309 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275154 | TAGGAGGTTTTTGTT[A/G]GTGAATCACCTCATT | 56916 |
rs759011599 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225896 | AAACCTATGTTATTT[C/T]GCAGTTTCCACTAAA | 56916 |
rs759025633 | snp | G/T | 1.65151e-05 | 0.00287355 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252962 | TTCTCAGAAAAAGGC[G/T]CAGAAGATAACAGAA | 56916 |
rs759029618 | snp | C/T | 0.000167687 | 0.00915507 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290677 | TGATATTTAACTCTT[C/T]ATTAAATCTTTCTTT | 56916 |
rs759077158 | in-del | -/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278369 | AATAATACTGTTATT[-/G]GCAATAATTTAAGTG | 56916 |
rs759081519 | snp | C/G | 3.31296e-05 | 0.00406985 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94233978 | ATCTGAAGATGAAGA[C/G]TCCCAAGGCCTTCCT | 56916 |
rs759128794 | snp | A/G | 6.93987e-05 | 0.00589021 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273584 | TTTTTTGTTTGTTTT[A/G]AAATGTTATATATTG | 56916 |
rs759130971 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246839 | GACTGAAGGTATATC[A/C]TTAAACCTGCCAAGA | 56916 |
rs759160252 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259041 | TATGGCTGGGCTTAT[A/G]GGCACATTACCCACA | 56916 |
rs759168915 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258223 | GCAGTGATGCGATCT[C/T]AGCTCACTGCAATCT | 56916 |
rs759175275 | snp | G/T | | | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94251316 | GATAGAGGAGAGGTG[G/T]TAAGGAAGAGTTGAG | 56916 |
rs759202612 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214518 | AGATCTGCCCGCCTC[A/G]GCCTCCTAAAGTGCT | 56916 |
rs759229489 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248892 | AGGTTGAAGAAGAAG[A/T]TTGTATTTTTCTCCA | 56916 |
rs759235821 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217130 | GCCAACATAATGGAC[A/G]TGAGTTTGTATCTCA | 56916 |
rs759289336 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275168 | TAGTGAATCACCTCA[C/T]TAATGGTGACTATAA | 56916 |
rs759300612 | snp | A/G | 6.60513e-05 | 0.00574641 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94249750 | TTTCCCAATTTTGAT[A/G]AACAGGTGAGTAGTC | 56916 |
rs759345298 | in-del | -/A | 1.7081e-05 | 0.00292237 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276491 | TAAGAGAATGTTTGT[-/A]AAGTTTTCCAAATTA | 56916 |
rs759351154 | snp | A/T | 6.58913e-05 | 0.00573945 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208496 | GCCTGGCCCTTCTTC[A/T]CCAATTTCTCTTAGT | 56916 |
rs759357875 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247414 | ATAAGCAGAGCTGGC[A/G]TAAGTGTGGGACCCA | 56916 |
rs759390492 | snp | G/T | 2.01461e-05 | 0.00317374 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273750 | AACTGTATTTAACTT[G/T]ATCATGTTTTATATA | 56916 |
rs759429185 | snp | A/G | 1.65603e-05 | 0.00287747 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94250781 | ACTCAAGGAACATGA[A/G]TGGATGTACACAGAA | 56916 |
rs759461767 | snp | C/T | 3.29815e-05 | 0.00406075 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94283235 | TGTTGTTATACTTCA[C/T]GATATTGACTGTAAT | 56916 |
rs759466036 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236612 | ATGCACACACAGGCA[C/T]GGAGTGGCCTGGACA | 56916 |
rs759489098 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268480 | TCAAGTTTCATTAGT[C/T]GTAAATTGTGAGCCT | 56916 |
rs759508856 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228490 | AGTACTATTATCTAA[C/T]ATACTTTTCATATTT | 56916 |
rs759513283 | snp | C/T | | | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291385 | AATGAGATTATCTTA[C/T]GTGCTTAATATTGCC | 56916 |
rs759515962 | in-del | -/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223459 | GATCACGCCACTGTA[-/C]TCTAGCCTGGGCGAC | 56916 |
rs759557988 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280475 | ATAAGTCTGTTACAC[-/T]TAAAAGGTTCTATGA | 56916 |
rs759602180 | in-del | -/TTGT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257592 | TTCCCCATCCCCAAA[-/TTGT]TTATTTACTTTTTGT | 56916 |
rs759608462 | snp | C/G | 3.30382e-05 | 0.00406423 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94264835 | TTCAAATAAATTGAC[C/G]AAACAAGTTACCATG | 56916 |
rs759615675 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266497 | TCTAAAACCTATATG[G/T]ATAGTCTCTTTAAAG | 56916 |
rs759623947 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287830 | TACATACTTTTTGAA[-/T]TTTTTTTATTACAGA | 56916 |
rs759631421 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276966 | CTGGGGAGGATAGAC[A/G]TGAAAGGAGTGGCTC | 56916 |
rs759671432 | snp | A/T | 3.38083e-05 | 0.00411133 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208617 | AATTGATGTAACATC[A/T]AGGACAGTTTTTAAA | 56916 |
rs759678403 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219076 | GTTGGCCTCCCAAAG[C/T]GCTGGGATTACAGGT | 56916 |
rs759694097 | snp | C/T | | | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94253086 | TAGTCAAGTTGTCTT[C/T]AGCCCAGGTAAGCAT | 56916 |
rs759697966 | snp | A/G | 1.75996e-05 | 0.00296639 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278373 | AATACTGTTATTGCA[A/G]TAATTTAAGTGAATA | 56916 |
rs759736021 | in-del | -/AACTC | 1.7184e-05 | 0.00293117 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281623 | TAGTTACAAAAAAAT[-/AACTC]ATTTATTATTATTGT | 56916 |
rs759739969 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230769 | TCCTAGGAAGCATTC[A/G]TAGACAAGAAAGAAC | 56916 |
rs759757049 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221900 | TTTTAGACAAAGAGC[A/C]ATAAATTTGAGAAGA | 56916 |
rs759758613 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291247 | TGGGTTCTTCCTGTA[A/G]TGCGCTATTATGTCT | 56916 |
rs759824226 | snp | C/T | 1.70819e-05 | 0.00292244 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264676 | TTTCCTAGATCTGAA[C/T]TATTCAATTATTTTT | 56916 |
rs759825594 | in-del | -/TCTT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286265 | CTGTTTTCAGCAGCC[-/TCTT]TCTTCTCTTCTATGA | 56916 |
rs759840633 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242588 | TGGCTGGTTCTAAAA[A/T]TATGCAAATCCTTTG | 56916 |
rs759842133 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219704 | TAAAACAAGTTAGCT[C/T]TTCCTATTGTTTTTA | 56916 |
rs759860816 | snp | A/G | 9.93888e-05 | 0.00704872 | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208217 | GCCTAACAATGAAGC[A/G]CAGCCATAACAGTCC | 56916 |
rs759882451 | snp | A/G | 1.64836e-05 | 0.0028708 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94281531 | TATCTTAGAGGTTCT[A/G]TTAAAACATCATCAG | 56916 |
rs759886317 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254298 | CTTGTTCTTCTTTTC[C/T]TCCTTTTCTTCTTTC | 56916 |
rs759914224 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277998 | CCATTTTTAGACCAA[A/G]TGATTTGCATCAGTC | 56916 |
rs759992757 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259691 | TTGTTATTACAAGAA[A/G]TTTAAGCACACAGTG | 56916 |
rs760046851 | in-del | -/CTT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288262 | TCTCTCATTTGTCCC[-/CTT]AATGTCTTTTATAGC | 56916 |
rs760061471 | snp | C/T | | | upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207574 | CGGCTCGCGCGTTGT[C/T]TGGGAAGAAAAAGCC | 56916 |
rs760074639 | snp | A/T | 1.65184e-05 | 0.00287384 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226197 | ATCAAAGAGGAATAC[A/T]GTATATTGATTTGTC | 56916 |
rs760149214 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262201 | TTTAACTAACCACTG[C/G]CTCTTTCTCGAAAAT | 56916 |
rs760195390 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212333 | GCTCATGCCACCATG[C/G]CCGGCTAATTTTTGT | 56916 |
rs760237788 | snp | C/T | 1.65551e-05 | 0.00287702 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252790 | ATCCAAAGAGAGTTG[C/T]TGAAGACTCTGAATA | 56916 |
rs760240664 | snp | C/T | | | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208596 | ACAGGTGAGTTACAA[C/T]GTTAAAATTGATGTA | 56916 |
rs760267308 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273130 | TATTTCCAGTGTTTG[G/T]CTATTAAGATAAAAC | 56916 |
rs760291157 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226927 | CAGGCTGCTCTCAGA[C/T]TCCTGGCCTCAAGCA | 56916 |
rs760321641 | snp | A/G | 2.34381e-05 | 0.00342323 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252679 | CTTCAAGAAGTCAAA[A/G]TTACCCTAAAAATGC | 56916 |
rs760325435 | snp | C/T | 8.25757e-05 | 0.00642503 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94276447 | GAATATGGGCTCCAT[C/T]CGCTACCAGCACCTT | 56916 |
rs760350721 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216994 | ATTTTTAATTTTTTG[C/T]GGAACCTCCATACCG | 56916 |
rs760367159 | snp | A/G | 3.62891e-05 | 0.00425949 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273575 | ATGTATTTATTTTTT[A/G]TTTGTTTTAAAATGT | 56916 |
rs760368061 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228051 | AGAAGTTAAGTGAAG[A/C]TAAAGTGTTGTAAGA | 56916 |
rs760389919 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272015 | AAATTTGTTCTTCAC[A/G]ATTCTGGAGGTGGAC | 56916 |
rs760450553 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240045 | TTCCATTTTTATTTT[A/G]TAATAGCCATGTTAA | 56916 |
rs760452926 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225985 | TAATTTTTTTCTTTA[A/T]AAAGTGGTGAGAATT | 56916 |
rs760491565 | snp | A/T | 1.6615e-05 | 0.00288223 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249638 | AATTGTTTTCTTTTT[A/T]TTTTCTCCCCATTAG | 56916 |
rs760503911 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250929 | AAGCTATTAGCTGTT[A/C]ATCAGAGGGTGGGAT | 56916 |
rs760512887 | in-del | -/AT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268113 | AACAGAACAGCAAAC[-/AT]ATATACACATTAATA | 56916 |
rs760541957 | in-del | -/TGAAGCAGATGTTCACCAATGTCAGCA | 0.000325256 | 0.0127484 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290036 | CATTTTATTGCTATT[-/TGAAGCAGATGTTCACCAATGTCAGCA]TGAAGCAGATGTTCA | 56916 |
rs760568508 | in-del | -/CTTCTTTATCAT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211479 | TGACTATTGACCTTA[-/CTTCTTTATCAT]GTGGTAACTTTTCAT | 56916 |
rs760625348 | snp | C/T | 1.75425e-05 | 0.00296158 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94273714 | TTCCAGCTTCAACTA[C/T]AGGTTTGTAATACTG | 56916 |
rs760640673 | in-del | -/TCT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288386 | CTTTTCCTTCTTTTC[-/TCT]TCTCCCTGCATTCTT | 56916 |
rs760642478 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281370 | ATTTTCTGCAAATTT[A/G]TCAACATGATATAAG | 56916 |
rs760695354 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248747 | GTCCAGATATCCATA[C/G]CATTTTATTGGTCTC | 56916 |
rs760783668 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224095 | GACTGTTTTATTACT[C/T]TGTGTATGATGATAA | 56916 |
rs760805792 | snp | G/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208481 | CCCTCAACCTTCCCA[G/T]CCTGGCCCTTCTTCA | 56916 |
rs760821210 | snp | C/T | 1.67447e-05 | 0.00289345 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94253020 | CTGGTAAGGCTTTAT[C/T]CTTTTTTTCCCCTTG | 56916 |
rs760824775 | snp | A/G | 1.64936e-05 | 0.00287168 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94249711 | GAAAAGCAGGAAAGT[A/G]TTGTACTGAAATTGC | 56916 |
rs760851041 | snp | A/G | 1.65567e-05 | 0.00287716 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208382 | TCCCTGCAAGGTGGT[A/G]CTTTCTACCAATATG | 56916 |
rs760945211 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211412 | CAAGATACTGAAGTT[A/G]GATTTTAAGGTCAGG | 56916 |
rs760981274 | snp | A/G | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94277032 | CACAGGCAAATAACC[A/G]TTTGCTGCTCACAGG | 56916 |
rs760997200 | snp | A/G | 1.66316e-05 | 0.00288367 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236919 | ATTCTTAAAGTGCTG[A/G]TTTAAAACATTAATC | 56916 |
rs761002026 | snp | A/G | 0.000352796 | 0.0132768 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291156 | ATTAATGTATTTTCA[A/G]TGATAGGCTGTTTCT | 56916 |
rs761019907 | snp | C/G | | | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94251760 | AAATAATGGTGTTAC[C/G]TTCATTCACAGGCAT | 56916 |
rs761056417 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242383 | CTGAGATGTTCAGCA[A/G]TGTACCTCTTCCCCA | 56916 |
rs761090905 | snp | A/G | 1.71578e-05 | 0.00292893 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264668 | CCTTTCTCTTTCCTA[A/G]ATCTGAACTATTCAA | 56916 |
rs761123676 | snp | A/G | 3.3018e-05 | 0.00406299 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237027 | GATGCAGGTATGCTT[A/G]ACTTAATTTTAAGCC | 56916 |
rs761137960 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257397 | ATCATCTTTTCTGTG[G/T]TTTTCAGTAACTTCA | 56916 |
rs761176346 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212747 | CTGCCTTGGCCTCCC[A/G]AAGTGCTGGGATTAC | 56916 |
rs761197777 | snp | A/T | 0.00027222 | 0.0116634 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208054 | TTATACTGGGGAACG[A/T]GCCTGCGCGTGCTTG | 56916 |
rs761206799 | snp | A/G | 1.6625e-05 | 0.00288309 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94250831 | TGTTTGCAGAAGACC[A/G]AGGTAATTATTCTGG | 56916 |
rs761213374 | snp | C/T | 3.29652e-05 | 0.00405974 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94281487 | GGTGATAGAGTTGTG[C/T]TATTTAGCCAATTTA | 56916 |
rs761238961 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218725 | TATTTATTAGAGAGT[A/T]TGATTCATCTTTTAT | 56916 |
rs761244082 | in-del | -/TCTT | 3.3753e-05 | 0.00410796 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208326 | TGGCCTTTTTTCCTC[-/TCTT]TATTTTTCCCCTGCA | 56916 |
rs761270075 | snp | C/T | | | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208956 | TATTCCCTCAAAATA[C/T]TGATCATCTACTGTG | 56916 |
rs761317738 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259250 | TAATTTTGGAAGCAA[C/T]ATACCAAATCTGAAT | 56916 |
rs761440595 | in-del | -/T | 0.00188616 | 0.0306516 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284949 | TGGACATATTTTGTA[-/T]TTTTTTTTAGAGAAG | 56916 |
rs761466241 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227853 | TTGCTATTTAAAGCC[A/G]TATGATCAGATGAAA | 56916 |
rs761483091 | snp | G/T | 1.65119e-05 | 0.00287327 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274844 | GAAATTAAAAATAAA[G/T]TACAGCACAATAAAT | 56916 |
rs761506359 | snp | A/T | 0.000282087 | 0.0118728 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289755 | TATGTAGTTCTGAAG[A/T]TGTTGAATAATCATT | 56916 |
rs761510785 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238264 | CAGTGTATCAAGATT[C/G]TTTTTTGTCTTCTAT | 56916 |
rs761520194 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285475 | GTGCATGTCAACTTA[C/G]GATACACTCTTCTGC | 56916 |
rs761528969 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232192 | TTCATGACATTATTT[-/A]TTTTCTATCACTTGT | 56916 |
rs761584585 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248416 | GTTAGATACTTGGAT[C/T]TGTTCCCTCCTCAGC | 56916 |
rs761595294 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249097 | ATGTATAGCCACAAT[A/T]CTCATATTAATTAAT | 56916 |
rs761624766 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271865 | ATAAGATTGCATTTG[C/T]TATCAAATGAGGTAT | 56916 |
rs761646211 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245633 | GTTTTTTGCCACTTT[A/G]CAATAACTCGTAAGC | 56916 |
rs761663278 | snp | A/T | 0.000162272 | 0.00900608 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290229 | ATTAATTCCTTCTGT[A/T]CATTTTCCAACTGCA | 56916 |
rs761678901 | snp | C/T | 1.7703e-05 | 0.0029751 | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94278886 | ATATTTCAACAGTTA[C/T]CCGCTTGGTTTTATT | 56916 |
rs761682389 | snp | A/G | 1.65488e-05 | 0.00287647 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226173 | AAGCAAGTATATCAT[A/G]TTTCAAAAATCAAAG | 56916 |
rs761706351 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215520 | TAGCCACTTGGGAGG[C/T]TGAGACAGAAGAATT | 56916 |
rs761708730 | snp | A/G | 1.65663e-05 | 0.002878 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94278647 | CCCCCAAGAAAGATC[A/G]AATTGAGTTGTGTGC | 56916 |
rs761747340 | in-del | -/CCTT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269283 | TAGCTATGTCCAGAC[-/CCTT]CCCTGTGTGCAAACA | 56916 |
rs761792537 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246813 | CCAGGAAAGTTACTC[-/T]TAACTCTGAAGACTG | 56916 |
rs761820406 | in-del | -/TA | 0.000349284 | 0.0132106 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290711 | TTCTGCCTGTCAGTC[-/TA]TATATTGCTGTTTTT | 56916 |
rs761822006 | in-del | -/ATC | 1.6906e-05 | 0.00290736 | cds-indel, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94240931 | CAGGAAAAGAAAATT[-/ATC]TTCTTCTTCAGAGCC | 56916 |
rs761823275 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211909 | TACCCCAGCTTTACT[G/T]TTATTTTTCTTCATA | 56916 |
rs761836763 | in-del | -/TTG | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217444 | GATTTTGATGTGTTT[-/TTG]TTGTTGTTGTTTTCT | 56916 |
rs761918523 | in-del | -/AGC | 1.64762e-05 | 0.00287016 | cds-indel, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208542 | GCTGAAGGGGAAGTT[-/AGC]AGGGCAAACACTCCT | 56916 |
rs761925685 | snp | A/G | 3.40015e-05 | 0.00412305 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208301 | GGCATTGTATCGTAT[A/G]TTGTTTTCATGGCCT | 56916 |
rs761940704 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235640 | GTCTGCTAATGTGAA[-/T]TTTTTTTTTTTTTTT | 56916 |
rs761957301 | snp | G/T | 1.68729e-05 | 0.00290451 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249626 | TGATATCTCTTAAAT[G/T]GTTTTCTTTTTTTTT | 56916 |
rs761965816 | snp | A/G | 1.74054e-05 | 0.00294998 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276503 | TGTAAAGTTTTCCAA[A/G]TTACTGTAAAATTTA | 56916 |
rs761967982 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250151 | TTAATATTTTATAAG[C/T]TTTCTACTACTTCCC | 56916 |
rs761974012 | snp | A/G | 1.64844e-05 | 0.00287087 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94285047 | ATTGAAACTAGAACA[A/G]GATATGACTACAGTA | 56916 |
rs761991845 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232988 | CCGTCTCAAAAAAAG[A/G]AAAAACACACATATT | 56916 |
rs761997804 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281192 | GTCCACATTTTCCGA[C/T]GTTTTTCTTATGAAA | 56916 |
rs762005180 | in-del | -/CA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245116 | AAGAATTTGATACTT[-/CA]GAGAAATTTTAAAAG | 56916 |
rs762011436 | snp | A/G | 1.65018e-05 | 0.00287239 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270854 | AGATTTGTTGTTGAA[A/G]GTGTCATTAAAAGGT | 56916 |
rs762027417 | snp | A/G | 1.79146e-05 | 0.00299282 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284912 | GTTTACATATATCCA[A/G]ATAACTATATTTAGT | 56916 |
rs762045251 | snp | G/T | 7.30273e-05 | 0.00604221 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241014 | TGGATCATGTAAGTT[G/T]ACATTTGAATTACAG | 56916 |
rs762076540 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264047 | AGAGAACCATTTATA[A/G]TATTATATTGAAATT | 56916 |
rs762076863 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264966 | ACAAAATATCTGAAT[A/T]TATTTCTGTATCGTG | 56916 |
rs762097635 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94209730 | ATTTACAAAGGCTTT[A/G]TCTAAGTAGTTTTGA | 56916 |
rs762108398 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238261 | CTACAGTGTATCAAG[A/T]TTCTTTTTTGTCTTC | 56916 |
rs762120626 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222433 | CATAGCTTTTCCTCA[C/T]CCAGCCCCCCACCCC | 56916 |
rs762142941 | in-del | -/TTC | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279855 | TGAAAGCAACCCATT[-/TTC]TTCCTTTTCTTTACT | 56916 |
rs762187616 | snp | C/T | 8.6077e-05 | 0.00655981 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264656 | AAATCAGGATTGCCT[C/T]TCTCTTTCCTAGATC | 56916 |
rs762195062 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210856 | CAAGAATTGCTTGAA[C/G]CTGGGAGGCAGAGGT | 56916 |
rs762217327 | snp | C/T | 1.66746e-05 | 0.00288739 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94253004 | TAATAGTTGGGAGGC[C/T]CTGGTAAGGCTTTAT | 56916 |
rs762227839 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285476 | TGCATGTCAACTTAC[A/G]ATACACTCTTCTGCA | 56916 |
rs762232273 | snp | A/T | 1.65206e-05 | 0.00287403 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276997 | TTTAAGAAAAAGCTA[A/T]TATAAATTTTACCTT | 56916 |
rs762279292 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282849 | ATTTAGCTAAGCCAC[A/C]AGTTTAAAAAGGACA | 56916 |
rs762320421 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218584 | CGCACCCAGACTCCT[G/T]TATGTTTCACCCTTT | 56916 |
rs762344277 | snp | C/T | 0.000132352 | 0.00813378 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94233991 | GAGTCCCAAGGCCTT[C/T]CTACCATGGCACGTA | 56916 |
rs762351866 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275307 | TACAAATAAGTATCT[C/G]TAATAAATACAATGA | 56916 |
rs762359751 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218449 | AGGCATGCATCACGA[C/T]GCCCAGCTAATATTT | 56916 |
rs762385886 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230559 | TTGTTGTGAGGTGCT[A/G]CCCTGTACATTTAGG | 56916 |
rs762386187 | snp | G/T | 1.74873e-05 | 0.00295691 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234165 | AATGATGATAAAATC[G/T]CTCCTGCATTCAGTG | 56916 |
rs762388383 | snp | A/G | 0.000615448 | 0.0175313 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291044 | TCTTCATGTGTTAAT[A/G]CTACCTCCTTGTACA | 56916 |
rs762413047 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216493 | AATTTACCATCTCAA[A/C]CATTTTTAAGTGTAC | 56916 |
rs762436076 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241627 | ATTCATACTTAGAGC[A/G]GGTTATCTGTTACTA | 56916 |
rs762472429 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289267 | AACCTTAGATTGCTA[A/T]GTTGGCAATATGAAC | 56916 |
rs762476200 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273524 | AAATCAAAAGTGAAT[A/G]CAGCACAGAATTACT | 56916 |
rs762484446 | in-del | -/CC | 0.000206975 | 0.0101708 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291047 | CATGTGTTAATACTA[-/CC]CCTCCTTGTACATCA | 56916 |
rs762489348 | in-del | -/TGT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269665 | CTATTGTTTTCATTC[-/TGT]TGTTGTTGTTGTTGT | 56916 |
rs762533205 | snp | C/T | 4.27113e-05 | 0.00462102 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273764 | TTATCATGTTTTATA[C/T]AGGTAGAAGAGAGTG | 56916 |
rs762545433 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282603 | TAAGGACGGAATTGT[G/T]TAGTATGTTTAAATT | 56916 |
rs762599551 | snp | C/T | 1.65018e-05 | 0.00287239 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274834 | TTTAACTTTGGAAAT[C/T]AAAAATAAAGTACAG | 56916 |
rs762615757 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283423 | GGCAAAGCATGGCTA[C/T]TGATGTATTTTATAC | 56916 |
rs762688868 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225333 | CCTTGTCTTCAAATG[A/G]CCTTTCCTTCTTTTG | 56916 |
rs762703091 | snp | C/G | 1.70507e-05 | 0.00291977 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208624 | GTAACATCAAGGACA[C/G]TTTTTAAAAGATGAA | 56916 |
rs762712147 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260751 | AAATTCAGAATAAAT[A/G]TTTATTCTTTCCTTT | 56916 |
rs762763672 | snp | A/T | | | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291638 | ACTTTATGCCAGTAG[A/T]TACTTACTTTGAAAC | 56916 |
rs762777218 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268820 | TGTATATTAAGCCCA[C/T]AGCATAGTCTGAAAT | 56916 |
rs762805381 | snp | A/G | 0.00556746 | 0.0524665 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289729 | TGAAATTTCAAAAAA[A/G]AAGCCACAAATATGT | 56916 |
rs762848269 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226715 | ATTAGAAATACAACA[A/G]TGAACAAACCATCCC | 56916 |
rs762856087 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270201 | CTGTGTACATTTGTA[C/T]GTAGTATGCACATAA | 56916 |
rs762867704 | snp | A/T | 1.65425e-05 | 0.00287593 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289606 | ACATTTACATTATGA[A/T]GACCATGGGGTTTAT | 56916 |
rs762915788 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254442 | TGTAAATACTTGCCC[A/G]AATATCTTATAGTAA | 56916 |
rs762946707 | in-del | -/CGAATATGGCCC | | | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208797 | TTTATATGAGTTCTT[-/CGAATATGGCCC]CATGGTGGAAGTTGA | 56916 |
rs763042686 | snp | C/G | 1.69821e-05 | 0.00291389 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94240977 | GAATTTAATGATGAT[C/G]AATCTATAAAAAAGA | 56916 |
rs763082908 | in-del | -/ATTT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254379 | CTTGTTGAGATTCTA[-/ATTT]ATTTAATAAGATATG | 56916 |
rs763083227 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239933 | TGGCAAGATTATCTG[C/G]TTTGAAGGTTTTTTT | 56916 |
rs763085576 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232778 | GCAGAAACTCTGGCA[G/T]TAGATAAAATCTCCT | 56916 |
rs763101241 | snp | A/G | 4.97203e-05 | 0.00498575 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264946 | TCGTATTTTATCTCA[A/G]TTATACAAAATATCT | 56916 |
rs763142008 | snp | A/T | 1.73893e-05 | 0.00294862 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94283132 | ACAGGATTCATCTAA[A/T]TGATGAGTTTAATAC | 56916 |
rs763150804 | in-del | -/A | 1.68354e-05 | 0.00290128 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276306 | AGCTCTTAAAGGTAT[-/A]AACCTTAGAGATGTT | 56916 |
rs763158660 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243926 | TGTTTTGAGTATTAA[G/T]GAGAAGCTTGAAACA | 56916 |
rs763191292 | snp | A/G | 1.65899e-05 | 0.00288005 | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94278767 | TCTTTTATGTGAAAA[A/G]GAATCTTGTACTGGG | 56916 |
rs763191790 | in-del | -/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282922 | AAGTAAGAGTTGGTA[-/G]GGGGTAGCAATATCG | 56916 |
rs763210841 | in-del | -/GT | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94290925 | AATAAAACTCTTACA[-/GT]GATTATTTAGATATT | 56916 |
rs763212560 | in-del | -/ATT | 1.66554e-05 | 0.00288573 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250836 | CAGAAGACCAAGGTA[-/ATT]ATTATTCTGGGTCAT | 56916 |
rs763236343 | snp | A/G/T | 5.83463e-05 | 0.00540095 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208287 | GAATAAACTGCTGTG[A/G/T]CATTGTATCGTATAT | 56916 |
rs763237151 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260347 | AATACTTTTTATTTT[-/A]TTTTTTTTTATTTTG | 56916 |
rs763240575 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220852 | TAATTTTATTAAATC[G/T]CAACTTAGGAGATGT | 56916 |
rs763248703 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249420 | AAGCACTGAGAATAA[A/G]GTTTGAGTTACCGGA | 56916 |
rs763264827 | snp | A/G | 1.65351e-05 | 0.00287528 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94276352 | AGATATAACTGTGCG[A/G]TCAGCAGTTCTGATG | 56916 |
rs763268521 | in-del | -/AAAG | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238617 | ACCCTGTCTCAAAAG[-/AAAG]AAAGAAAGAAAGAAA | 56916 |
rs763298692 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288085 | GTGTTTGTTTTTTCT[A/G]CTTCTTTTTTCCCAT | 56916 |
rs763301208 | snp | A/C | 6.61781e-05 | 0.00575193 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276985 | AAGGAGTGGCTCTTT[A/C]AGAAAAAGCTAATAT | 56916 |
rs763323332 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214937 | TCGTCAGAAAGATTT[C/T]CTGAGAGTATTGCTC | 56916 |
rs763338528 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94263754 | ACATGAATAAAAATC[A/G]TGTGGTATTTTCCTA | 56916 |
rs763375614 | snp | C/G | 3.33489e-05 | 0.0040833 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208352 | CCCCTGCAGATAGTT[C/G]ATTTAAAGCCCCCAT | 56916 |
rs763377432 | snp | C/T | 1.66087e-05 | 0.00288168 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283319 | GTAAGTGTTTTTAGT[C/T]GGAATGTATTTTTAA | 56916 |
rs763428979 | in-del | -/TC | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286310 | TCCTCAGACTCATGT[-/TC]TCTCCAAAGAGAATA | 56916 |
rs763447174 | snp | A/G | 1.65002e-05 | 0.00287225 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252812 | CTCTGAATATGATTC[A/G]GGTTCTGATGTCGGT | 56916 |
rs763508390 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240102 | ATGTATTTGAGCTGC[A/G]TAGTTAGGGCTCTGA | 56916 |
rs763545178 | in-del | -/T | | | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207045 | ATGCCTGTATCAAAA[-/T]ATCTCATGTACCCTA | 56916 |
rs763563297 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287129 | CTGGCCTCTCCTTAC[C/T]ACTTTTCCTAGAAGT | 56916 |
rs763572875 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265886 | TAGCAGTAGGATCTC[A/G]TTAAAATTAATTGCC | 56916 |
rs763579930 | in-del | -/TTTTTATTGT | 1.66735e-05 | 0.00288729 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278543 | TCTACATGTTTTTTA[-/TTTTTATTGT]TTTTAAAACTTAGGT | 56916 |
rs763599878 | in-del | -/TTT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282101 | AAATACGTTTTTTTG[-/TTT]TTTTTTTTTTTTTTG | 56916 |
rs763604526 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282758 | TCATGAAGTCCTTGA[C/T]TCATCAGAAATGTTG | 56916 |
rs763616471 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237273 | CTCTTTTTAAAGTAT[A/G]ATTTCTAGTTGCATT | 56916 |
rs763619162 | snp | C/G | 1.64841e-05 | 0.00287085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274696 | ACCATGTGAACATAC[C/G]CTATTGTAGCAGATG | 56916 |
rs763651190 | snp | A/G | 0.000364528 | 0.0134956 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94250813 | CTTTAGAATCTCTAA[A/G]AGTGTTTGCAGAAGA | 56916 |
rs763671461 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248237 | TATACTACAATGTTC[A/G]TTCATGTTGTGGTGT | 56916 |
rs763681907 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283543 | AGTATTAACAATTGA[C/T]GGCCGGGCGCCGTGG | 56916 |
rs763696423 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227041 | AAAGAGCGTGGTCAG[-/A]AAAGCCTCAATTGAG | 56916 |
rs763748249 | snp | A/G | 1.65682e-05 | 0.00287817 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249768 | CAGGTGAGTAGTCGT[A/G]TATGAAAATTTAATC | 56916 |
rs763781746 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216693 | ATTCTAAGTATCTCA[-/T]TAAAGTGGAATCATC | 56916 |
rs763792881 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229743 | GACCTAGGAAATACT[C/T]GGGTGTAGGGGGTTG | 56916 |
rs763810912 | snp | A/G | 1.66824e-05 | 0.00288806 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289614 | ATTATGATGACCATG[A/G]GGTTTATGAACATTT | 56916 |
rs763824464 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235800 | TACTTTCACTTGATT[A/G]CCAATTTTTAATGTA | 56916 |
rs763856519 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225472 | ATATAGTCACAAAGA[G/T]TAGGGCCCACACACA | 56916 |
rs763874154 | in-del | -/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224380 | CTTGGGACCAGAAAT[-/G]TTTCTCATTTTAGAT | 56916 |
rs763912461 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219223 | AACAGTGTAGAGCAA[C/T]ACATGATTTGAATAT | 56916 |
rs763912999 | snp | A/G | 3.4333e-05 | 0.0041431 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278399 | GAATAATTCCTAAAA[A/G]GATATGTTTTTATTT | 56916 |
rs763976142 | snp | A/C | | | intron-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94253450 | GCTCCATGATTCAAA[A/C]TGCCAGCCTAAGTGT | 56916 |
rs764061007 | in-del | -/AA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262449 | ATTGTCTCTCAACTC[-/AA]AGCCTTCTTAATAGT | 56916 |
rs764108345 | in-del | -/TTA | 0.00026116 | 0.0114242 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281629 | AAAAAAATAACTCAT[-/TTA]TTATTATTATTGTTA | 56916 |
rs764184503 | snp | A/G | 1.65789e-05 | 0.0028791 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94278627 | TCAGGTTCTCAAGCA[A/G]TTACCCCCCAAGAAA | 56916 |
rs764218827 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277289 | TAAGTAGGTGATAAC[A/T]CTATATTTGGATTGG | 56916 |
rs764222577 | snp | C/T | 7.5543e-05 | 0.00614539 | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208231 | CGCAGCCATAACAGT[C/T]CTGAGCCACTGGCAT | 56916 |
rs764233769 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238021 | TCTAAGTGGATTCTT[-/A]ACTACTATTAATTTT | 56916 |
rs764237106 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207664 | GGTCCCGGCACGGCT[A/G]CCGTCGCCCCACGCT | 56916 |
rs764279551 | in-del | -/TTAT | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94290929 | AAACTCTTACAGTGA[-/TTAT]TTAGATATTAAAGAC | 56916 |
rs764284011 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219794 | GCACAAATTATGCTT[A/G]TAACATAGTTACTCA | 56916 |
rs764311693 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220965 | GCAATTGCTTTGTGC[C/T]AACCAGTCACGTTTC | 56916 |
rs764321377 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262434 | CCAACACAGACCACT[A/G]TTGTCTCTCAACTCA | 56916 |
rs764324755 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276483 | AATTAATGTAAGAGA[A/G]TGTTTGTAAAGTTTT | 56916 |
rs764329828 | in-del | -/T | 1.68645e-05 | 0.00290379 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208328 | GCCTTTTTTCCTCTC[-/T]TTATTTTTCCCCTGC | 56916 |
rs764341805 | snp | C/T | 1.69206e-05 | 0.00290861 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94283145 | AATTGATGAGTTTAA[C/T]ACCGATATGGATATC | 56916 |
rs764352624 | snp | C/T | 3.30579e-05 | 0.00406544 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94276357 | TAACTGTGCGATCAG[C/T]AGTTCTGATGACCGT | 56916 |
rs764363464 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250145 | AGTGTCTTAATATTT[C/T]ATAAGCTTTCTACTA | 56916 |
rs764379408 | snp | A/G | 1.70583e-05 | 0.00292042 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94240983 | AATGATGATCAATCT[A/G]TAAAAAAGACAAGAC | 56916 |
rs764475350 | snp | A/G | 2.12024e-05 | 0.00325588 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252710 | AACTAAAACAAAACT[A/G]AAACAGAAATTTTCA | 56916 |
rs764496250 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276262 | AAATAAAAAATGATT[A/T]TATAAGACATTAAAT | 56916 |
rs764504577 | in-del | -/ATG | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216457 | TTAATTTTAAAAATT[-/ATG]ATAAAATACACATAA | 56916 |
rs764521045 | snp | C/G | 1.64985e-05 | 0.0028721 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252813 | TCTGAATATGATTCA[C/G]GTTCTGATGTCGGTA | 56916 |
rs764522931 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240436 | AAAATGTTACCTACT[A/T]TGTAGGTTTGTGTGT | 56916 |
rs764549424 | snp | A/G | | | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209555 | TGAAAGATTGGTAAC[A/G]CACATGTTTATCCTT | 56916 |
rs764580020 | snp | C/T | 0.000162456 | 0.0090112 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290409 | TGCATCAGCAAAATG[C/T]TGGTGACATTTTTCT | 56916 |
rs764689522 | snp | C/G | 1.65647e-05 | 0.00287786 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226312 | GTAAGCTGATTAATA[C/G]ATATATTGTATTTGC | 56916 |
rs764707184 | snp | A/T | | | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291434 | AACTTACTACTTAGG[A/T]TGTATTCTCATTGGT | 56916 |
rs764732491 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287989 | GACTCCATCTCTATT[A/C]AAATATATATATATT | 56916 |
rs764734162 | snp | C/G | 1.66674e-05 | 0.00288676 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280584 | ACTGTGTTTTGTTTT[C/G]TTTTAAGGAACCTAC | 56916 |
rs764736942 | in-del | -/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232424 | TCATTTTCTCAGTCA[-/C]CCTAAGAGGCAAGGT | 56916 |
rs764800740 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258257 | CCTCCCACGTATAAG[C/T]GATTCTCCTGCCTCA | 56916 |
rs764810625 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259074 | ATATTAAGACTAACT[A/G]TTTTAGCCTCCCTTG | 56916 |
rs764818312 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229373 | TGTGCTTTTATTTAT[A/G]TGGTACAATAAATAT | 56916 |
rs764836005 | snp | C/T | 2.01384e-05 | 0.00317313 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273752 | CTGTATTTAACTTTA[C/T]CATGTTTTATATAGG | 56916 |
rs764838178 | snp | A/C | 6.60546e-05 | 0.00574656 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94249665 | TTAGGGAGAGGAATC[A/C]AATGAGTCTGCAGAA | 56916 |
rs764851120 | in-del | -/T | | | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94251658 | GTATGATAATCTGTG[-/T]TAAGTCTAATAGCTT | 56916 |
rs764886010 | snp | C/T | 1.65625e-05 | 0.00287766 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94233980 | CTGAAGATGAAGAGT[C/T]CCAAGGCCTTCCTAC | 56916 |
rs764897871 | in-del | -/T | 0.000326291 | 0.0127687 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94290919 | AGGCAAATAAAACTC[-/T]TTACAGTGATTATTT | 56916 |
rs764923887 | snp | A/T | 3.43318e-05 | 0.00414303 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273585 | TTTTTGTTTGTTTTA[A/T]AATGTTATATATTGT | 56916 |
rs764962944 | snp | C/T | 9.93361e-05 | 0.00704686 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249765 | AAACAGGTGAGTAGT[C/T]GTGTATGAAAATTTA | 56916 |
rs765003415 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281626 | TTACAAAAAAATAAC[G/T]CATTTATTATTATTG | 56916 |
rs765006035 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280066 | GATGGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 56916 |
rs765017365 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265689 | AATACTTCCCTTTTT[-/A]AAAAAAAATAATATA | 56916 |
rs765021818 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225190 | AACTGCCATAACAAA[A/G]TGCTACAGGTTCGGT | 56916 |
rs765028545 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241287 | CAGCTAAGCCAGATA[A/T]TTTGTGCTTGCATAT | 56916 |
rs765068611 | snp | C/G | 1.69539e-05 | 0.00291147 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208620 | TGATGTAACATCAAG[C/G]ACAGTTTTTAAAAGA | 56916 |
rs765081814 | snp | A/G | 5.04325e-05 | 0.00502132 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285119 | TCTATATGACCATGC[A/G]TCTAATTAGTCAGTG | 56916 |
rs765157379 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211767 | CTTTTTTGCCTGGAA[G/T]ACTCTTCCTGCTGAT | 56916 |
rs765178930 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233324 | GATTTTTTTGTTTAG[A/G]GAATAAATGAGTAAA | 56916 |
rs765215230 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94263446 | TATGAATTTTGTCCC[G/T]GTGAAAAATATAGAG | 56916 |
rs765222271 | in-del | -/AGG | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245480 | CAGCTTTAGTGTAAA[-/AGG]AGGAGGCTGGCAACA | 56916 |
rs765236441 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257594 | CCCATCCCCAAATTG[-/T]TTTATTTACTTTTTG | 56916 |
rs765241263 | snp | A/T | 1.75801e-05 | 0.00296475 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278377 | CTGTTATTGCAATAA[A/T]TTAAGTGAATAATTC | 56916 |
rs765244051 | snp | A/G | | | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291470 | CATTGGACTGATGTC[A/G]GTAAATACTGTAACC | 56916 |
rs765320730 | in-del | -/T | 0.025065 | 0.109107 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249633 | TCTTAAATTGTTTTC[-/T]TTTTTTTTTCTCCCC | 56916 |
rs765368591 | snp | A/G | 0.00178499 | 0.0298213 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290349 | GTCACTTCTGCTCCA[A/G]TTCTCTTCCTCTCTA | 56916 |
rs765391834 | in-del | -/C | 0.000185822 | 0.00963724 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213014 | ATTTCTCCTTTTTTT[-/C]TTTGACTTTTGGGAG | 56916 |
rs765392820 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246116 | TCATAACTGACATTC[-/T]TTTTTTTTTTTTTTT | 56916 |
rs765401237 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218991 | TAATTTTTGTGTTTT[A/T]AGTAGGGACAGGGTT | 56916 |
rs765420909 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287923 | TTGGGGAGACAGGCG[A/G]GAGGATCGTTTGAGC | 56916 |
rs765440385 | snp | G/T | 0.000214431 | 0.0103523 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208077 | CGTGCTTGGGTAAGA[G/T]GAGGTTGCATGAGGG | 56916 |
rs765496040 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221967 | AACTTTTAGGGGAGT[C/T]ACTAGGAGACATATG | 56916 |
rs765506477 | snp | A/G | 1.65222e-05 | 0.00287417 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94264848 | ACCAAACAAGTTACC[A/G]TGCTTACTGGAAATG | 56916 |
rs765534240 | in-del | -/TT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226510 | TGGATAACAGTGATT[-/TT]TTTTTTTTTTTTTTT | 56916 |
rs765567365 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219736 | ATGGAAGGACAGGCT[A/G]TTTTCCCTCCTGTTC | 56916 |
rs765600712 | snp | G/T | 1.65367e-05 | 0.00287543 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274875 | AGTCATGTGTTTATT[G/T]TTTTTAAATTCTAGG | 56916 |
rs765639196 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278076 | TTTCTACCCCCCACG[A/C]TCCTCCTTACCCACA | 56916 |
rs765684834 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261424 | ATGTTATTAGATGAA[G/T]ATTTACCTCTCCATG | 56916 |
rs765716626 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212556 | CAGTGGCACAATCTC[A/G]GCTCACTGCAACCTC | 56916 |
rs765761637 | snp | C/T | 4.36767e-05 | 0.00467295 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208279 | TGCCTTGGGAATAAA[C/T]TGCTGTGGCATTGTA | 56916 |
rs765788662 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238657 | AACCTCCTGAAAAAT[A/G]ATACGCTCAGTGAAC | 56916 |
rs765805221 | snp | C/T | 4.63596e-05 | 0.00481432 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252685 | GAAGTCAAAATTACC[C/T]TAAAAATGCAACTAA | 56916 |
rs765833133 | snp | C/T | 0.000162377 | 0.00900901 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290378 | TAAATAGTAGTTTAT[C/T]ACTGCCACATCTCCA | 56916 |
rs765852620 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272155 | ACATGCCTGATATTT[C/T]TTCTTACAAGGACAG | 56916 |
rs765863311 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222779 | ACCAGCCTGGCAAAC[A/G]TGGTGAAACCCAGTC | 56916 |
rs765867546 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279294 | TGGGACTACAGGCAC[A/G]CACCACCATGCCCGG | 56916 |
rs765886713 | snp | A/G/T | 0.000324267 | 0.0127298 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289943 | TATTTGACAATGCTT[A/G/T]TGTCTTGTTTTTGCT | 56916 |
rs765921860 | snp | A/G | 3.29957e-05 | 0.00406162 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270704 | ATATAGATGTGTAAT[A/G]TTTGGTAACTCTCTC | 56916 |
rs765933881 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271021 | AGATAGATTTATTGT[C/G]TTTCTGATTATCAGA | 56916 |
rs765935542 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248825 | AATTTAGTTATTTCT[A/G]TCTAAGGTACTGAAA | 56916 |
rs765937459 | snp | G/T | 1.65157e-05 | 0.0028736 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226205 | GGAATACAGTATATT[G/T]ATTTGTCTTCTGATA | 56916 |
rs765953632 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226983 | TGCTGGGATTACAGG[C/T]GTTAGACACCACACC | 56916 |
rs765988474 | in-del | -/TATT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276750 | TTCTATATGTTAAAC[-/TATT]TATAAATAATCTTTC | 56916 |
rs765988956 | snp | C/T | 1.74756e-05 | 0.00295593 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280559 | ATTAATTATTTTTAT[C/T]TTGAAGTATACTGTG | 56916 |
rs765993436 | snp | A/G | 0.000164136 | 0.00905766 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290659 | GAAGTGAAGTTGTCT[A/G]TTTGATATTTAACTC | 56916 |
rs765993764 | in-del | -/AACATCAGTG | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270114 | TTTAGCATTTGCTAA[-/AACATCAGTG]AACATCAGTGAACAT | 56916 |
rs766064859 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212361 | TGTATTTTCTGTAGA[C/G]ACGGCATTTCGCTAT | 56916 |
rs766079809 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233289 | GCCTACCATGTTTGA[A/G]AACCAAAATTTCAAA | 56916 |
rs766134493 | snp | A/G | 3.30398e-05 | 0.00406434 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226278 | AGAAAACATTCAACA[A/G]AGATACAGTGATTAT | 56916 |
rs766143552 | in-del | -/T | 1.80628e-05 | 0.00300517 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250883 | TCATTATAGTCTGTA[-/T]TTTAGTATATAAGAA | 56916 |
rs766188781 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274296 | GTCTGTGATAAAAAC[A/G]ATCGCCATGGTATTT | 56916 |
rs766190695 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228080 | GAAAGAGCAAGAGAT[C/T]GGACTGTCTACTTCT | 56916 |
rs766210807 | snp | A/G | 1.65029e-05 | 0.00287248 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285081 | GAAGGTGAGTTGTTT[A/G]TAAGCAGAAACTTCA | 56916 |
rs766219199 | snp | A/G | 1.64942e-05 | 0.00287173 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94249714 | AAGCAGGAAAGTATT[A/G]TACTGAAATTGCAAA | 56916 |
rs766290703 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288475 | GGCTATTTTCAAGTC[C/T]GTGGATGAGCTTGGA | 56916 |
rs766311115 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288451 | TGAAGTGTCAATTTG[A/G]ATTTTATGGGCTATT | 56916 |
rs766331484 | snp | C/T | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94277050 | TGCTGCTCACAGGCA[C/T]ACCTGTACAGAACAA | 56916 |
rs766343853 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255683 | TGTCAGATAATTATG[C/T]TTTTTGAAACTAAAA | 56916 |
rs766417188 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208483 | CTCAACCTTCCCAGC[C/T]TGGCCCTTCTTCACC | 56916 |
rs766452345 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281379 | AAATTTATCAACATG[A/G]TATAAGTAACACTTC | 56916 |
rs766457237 | in-del | -/AA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285767 | AGGTGGGCGGTAGAG[-/AA]AGTTTGAGTAAGAAG | 56916 |
rs766535861 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229789 | AGAAGGAAAAATGTG[A/G]AAATGTGTGGTGTTT | 56916 |
rs766541470 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94209999 | TTTGAAATCTGTGAT[C/G]CACACTTTTTTCATC | 56916 |
rs766548781 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243419 | GATGATGGGTTGCTG[C/T]TGCCAATGCTCCGTT | 56916 |
rs766583041 | snp | A/T | 1.65436e-05 | 0.00287602 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94234008 | TACCATGGCACGTAG[A/T]AATGATGATATTTCA | 56916 |
rs766586740 | snp | G/T | 1.71419e-05 | 0.00292757 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264670 | TTTCTCTTTCCTAGA[G/T]CTGAACTATTCAATT | 56916 |
rs766589133 | in-del | -/T | 1.67184e-05 | 0.00289118 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276319 | ATAACCTTAGAGATG[-/T]TTTTTTCTTTTGGTG | 56916 |
rs766589219 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276857 | TGCTGTTGATAATAG[C/T]GGACGTCAATTATTT | 56916 |
rs766590852 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241810 | TAGAAAGTCTTACCT[A/T]GTTGACTTGCATGCA | 56916 |
rs766641134 | snp | C/T | 1.64982e-05 | 0.00287208 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277196 | CTCCCAAATATGTTA[C/T]TTGTGTTTTATCTGG | 56916 |
rs766653523 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289641 | ATTTATAACTTTTTA[C/T]AATTTCCATATTACA | 56916 |
rs766687311 | snp | C/T | | | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209303 | TGCACAATAATCCTA[C/T]AAGGTAGATATTACT | 56916 |
rs766699138 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230727 | CCACTGATGTGTATG[C/T]TAGAAACTCTGGCAG | 56916 |
rs766726558 | snp | C/T | | | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94205691 | CGTGTGCCATCATGC[C/T]TGGATAACTTTGTAT | 56916 |
rs766742428 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232974 | GACAGAGTGGAACCC[A/C]GTCTCAAAAAAAGAA | 56916 |
rs766745727 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254859 | AGAACTTTGAGCTCC[-/T]ACTTTAAAAACCTTT | 56916 |
rs766770306 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211547 | TAGTTTATTTACAGT[A/G]AAGTGTCAGGTCAAA | 56916 |
rs766809075 | snp | A/G | 6.61299e-05 | 0.00574983 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280789 | ACAGAAGGTATTAAA[A/G]AAGAATGGCGTTTCT | 56916 |
rs766827377 | snp | G/T | 0.000520698 | 0.0161269 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208058 | ACTGGGGAACGTGCC[G/T]GCGCGTGCTTGGGTA | 56916 |
rs766850018 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218807 | CAGATTTTATAGTCT[A/G]TTGTTTTGGTAATAA | 56916 |
rs766891204 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273867 | TTTATACTTTTCTCC[-/T]TTTGTTTATATATGT | 56916 |
rs767002266 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247622 | CCATCATTCCTGTCT[A/G]GTTCCAAACGCTGTC | 56916 |
rs767004791 | snp | C/T | 1.70295e-05 | 0.00291796 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250867 | AGAAAATACATACTT[C/T]TCATTATAGTCTGTA | 56916 |
rs767004806 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244459 | TGATTAAACAAATAT[A/C]TGTTATGAACGCATG | 56916 |
rs767054675 | snp | A/G | 3.31192e-05 | 0.00406921 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94278663 | AATTGAGTTGTGTGC[A/G]ATGTCGGAGAAGCAG | 56916 |
rs767060148 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271378 | TCACAAAGTTTGTTA[C/T]AGCCAGTAGTCCAGG | 56916 |
rs767064469 | snp | A/G | 1.65381e-05 | 0.00287555 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226179 | GTATATCATATTTCA[A/G]AAATCAAAGAGGAAT | 56916 |
rs767116321 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213300 | AAAGTCACAGAGATA[G/T]GACCTTTGGAGTGGA | 56916 |
rs767158561 | in-del | -/TGT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269667 | TTGTTTTCATTCTGT[-/TGT]TGTTGTTGTTGTTGT | 56916 |
rs767248430 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286383 | TGGGCAAGCTTTAGA[C/T]ATCTTACCTGTTCAA | 56916 |
rs767250448 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232733 | CAAGGCGGGCGGATC[A/G]CTTGAGCCTAGGAGT | 56916 |
rs767257112 | in-del | -/A | 0.000148715 | 0.00862179 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276995 | CTTTAAGAAAAAGCT[-/A]AATATAAATTTTACC | 56916 |
rs767275940 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214513 | ACTTGAGATCTGCCC[A/G]CCTCGGCCTCCTAAA | 56916 |
rs767311457 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288147 | CAATTTATTTTCAAT[A/G]TCACAGCATATTCCT | 56916 |
rs767337212 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271881 | TATCAAATGAGGTAT[A/G]TATTATGTGAAACTA | 56916 |
rs767398020 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246853 | CATTAAACCTGCCAA[A/G]ATAAAAACGGATTGT | 56916 |
rs767451718 | in-del | -/TG | 5.04995e-05 | 0.00502466 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94253037 | TTTTTTCCCCTTGTA[-/TG]TGTGTGTGTGTATTT | 56916 |
rs767455327 | snp | A/G | 1.78487e-05 | 0.00298731 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284919 | TATATCCAAATAACT[A/G]TATTTAGTAACCAAT | 56916 |
rs767503782 | snp | G/T | 3.3065e-05 | 0.00406588 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270686 | AATAGAAAACTGATA[G/T]AAATATAGATGTGTA | 56916 |
rs767511151 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233002 | GAAAAAACACACATA[C/T]TCTGTTCTTTGGAAA | 56916 |
rs767538998 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279824 | TTAACCTTATTTATC[C/T]TTACTGATCTTTGGT | 56916 |
rs767562241 | snp | A/G | 5.4811e-05 | 0.00523474 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241015 | GGATCATGTAAGTTT[A/G]CATTTGAATTACAGT | 56916 |
rs767564176 | in-del | -/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281246 | AAATCAAAACTGAGA[-/G]CTAGCTTTTAGCCCT | 56916 |
rs767670844 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234171 | GATAAAATCTCTCCT[G/T]CATTCAGTGCTATAG | 56916 |
rs767672787 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221209 | GAAGATCAATGGTGA[C/T]ATTAACAAAAGTAAT | 56916 |
rs767682379 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240564 | ACTTACACTTGGTGG[G/T]GGTCAGCTTTATTTC | 56916 |
rs767683521 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262539 | CTCTAAAACCCTTCA[A/G]TAGCTTTTTAATGCC | 56916 |
rs767690137 | snp | C/T | | | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208995 | ATTGAGCAAGGTGCC[C/T]AAAGACAACCTCTGT | 56916 |
rs767696757 | snp | C/T | 3.29587e-05 | 0.00405934 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277019 | TTTTACCTTCATTCA[C/T]AGGCAAATAACCGTT | 56916 |
rs767696967 | snp | G/T | 1.64855e-05 | 0.00287097 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252829 | GTTCTGATGTCGGTA[G/T]TTCACTAGATGAGGA | 56916 |
rs767706633 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289317 | CCCTAATCTAAGTAG[A/G]GCTTAGGAAAGTTTT | 56916 |
rs767710291 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94209744 | TGTCTAAGTAGTTTT[A/G]AATTTAAATGCTATA | 56916 |
rs767720241 | in-del | -/AA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261611 | AATTGGTGAAAGATT[-/AA]GTTTGTTTGTTTGTT | 56916 |
rs767720734 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94290959 | AGACTGAGAACTCAC[A/G]GCTTAACCCCAGTCT | 56916 |
rs767754648 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249632 | CTCTTAAATTGTTTT[C/T]TTTTTTTTTTCTCCC | 56916 |
rs767823348 | snp | A/G/T | 3.34797e-05 | 0.00409132 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94253016 | GGCTCTGGTAAGGCT[A/G/T]TATTCTTTTTTTCCC | 56916 |
rs767829523 | snp | C/T | 1.64846e-05 | 0.0028709 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94285050 | GAAACTAGAACAGGA[C/T]ATGACTACAGTAGAT | 56916 |
rs767846057 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217436 | GTATCCTAGATTTTG[A/G]TGTGTTTTTGTTGTT | 56916 |
rs767885159 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255349 | TGAATAAAGTACATA[-/T]ATACAATAGTAATTT | 56916 |
rs767908475 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222434 | ATAGCTTTTCCTCAC[C/T]CAGCCCCCCACCCCC | 56916 |
rs767945107 | snp | C/T | 0.000171807 | 0.00926681 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290806 | TCATTATAAATAAAC[C/T]TATTTATAAATCAAA | 56916 |
rs767950479 | snp | A/G | 1.65614e-05 | 0.00287757 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94280605 | AGGAACCTACACATT[A/G]TGAGGCTAACCCTGA | 56916 |
rs767970443 | in-del | -/AGTT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280978 | ACAAAAACAATAGAA[-/AGTT]AGTTAGTAGACTGTA | 56916 |
rs767978480 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288110 | TCCCATTGATCCATA[A/G]TAAAGTCAATTGTAA | 56916 |
rs768025844 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231559 | AGTTGTTTTCCTTAT[G/T]TGTTTATTGTGTCAC | 56916 |
rs768060013 | snp | C/T | 1.67091e-05 | 0.00289038 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236902 | TTTCAGTAACTGAAA[C/T]AATTCTTAAAGTGCT | 56916 |
rs768091384 | snp | C/T | 6.5987e-05 | 0.00574362 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94236997 | GCAATTGCTGCTGCC[C/T]TGCTGATGTTTGGTG | 56916 |
rs768125147 | snp | C/G | 1.64855e-05 | 0.00287097 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94280752 | AATTTCGAGTTTTAG[C/G]ATGCATCTTGTCTGA | 56916 |
rs768157974 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258364 | TTCATGATGTTGGCC[A/G]GGCTGGTCTTGAACT | 56916 |
rs768213818 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221040 | TAGGAATTTGGCAGA[A/T]GTTTTCTCAAAATGA | 56916 |
rs768214878 | snp | A/G | 0.000115408 | 0.00759543 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281456 | CTATTTCTAATTCAT[A/G]TATGTATTTTCACAG | 56916 |
rs768217951 | snp | C/G | 3.59693e-05 | 0.00424068 | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208196 | GTCCACCTTCTAATT[C/G]TTGCGGCCTAACAAT | 56916 |
rs768252025 | snp | A/C | | | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209021 | TCTGTACACAAGGGA[A/C]GATCAGATCACATCA | 56916 |
rs768259106 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219570 | TGTCTTCTTTTATGC[A/G]TACCACTCATACCAC | 56916 |
rs768261908 | in-del | -/AGTG | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231042 | GACATTATTGTCCTT[-/AGTG]AGAACAGTTTCACTG | 56916 |
rs768265911 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277709 | AGTTTTTTCAATACC[G/T]CAGTGTTTACACTGA | 56916 |
rs768265968 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260777 | CCTTTAATTTTCCAG[C/T]TCTCAAAGTGATTGG | 56916 |
rs768288875 | snp | C/T | 6.7611e-05 | 0.00581386 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208261 | TGTTTGCGGGCCCTT[C/T]ATTGCCTTGGGAATA | 56916 |
rs768297758 | in-del | -/TCTT | 0.00016862 | 0.0091805 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290684 | TAACTCTTTATTAAA[-/TCTT]TCTTTAAATTTCTGC | 56916 |
rs768352428 | snp | A/G | 5.05983e-05 | 0.00502957 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276302 | CTCCAAGCTCTTAAA[A/G]GTATAACCTTAGAGA | 56916 |
rs768364140 | snp | C/G | | | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206902 | GTGCTGGGATTACAG[C/G]CGTGAGCCACCACTC | 56916 |
rs768378897 | snp | C/T | 1.91393e-05 | 0.00309343 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240879 | TATTTCTGTGCAAAG[C/T]TTGAGTGTGCTGCTC | 56916 |
rs768385881 | snp | G/T | 1.64939e-05 | 0.0028717 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94276403 | CTGAAACTTAATTAC[G/T]CAATTTTTGATGAGG | 56916 |
rs768421869 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232452 | GGTCAAGTAGGGAGC[A/G]GGGAATATAGAGAGG | 56916 |
rs768435230 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286497 | GCCTTGCATTTCCCA[C/T]CTGCAGACACTTAAG | 56916 |
rs768435639 | in-del | -/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265126 | TCATTATAAATTAAA[-/G]GGGGGGGATGGTATG | 56916 |
rs768446855 | snp | C/T | 3.54359e-05 | 0.00420912 | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94278874 | AACTTAGTTGATATA[C/T]TTCAACAGTTATCCG | 56916 |
rs768509918 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273391 | GTATATGAACTAGCA[A/G]TGAAGATCTATCCAC | 56916 |
rs768526431 | snp | C/T | 0.000162404 | 0.00900974 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290131 | TCCTCTCAAGTACTT[C/T]TGCTGAAACAAATTT | 56916 |
rs768527455 | snp | C/T | 3.30109e-05 | 0.00406256 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226248 | TTTCCCCAAATTGCT[C/T]CAATACAGTTCAAGA | 56916 |
rs768544433 | snp | C/T | 1.64906e-05 | 0.00287142 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94249693 | GAATCTAGCAGTAAT[C/T]GGGAAAAGCAGGAAA | 56916 |
rs768546456 | snp | A/T | 2.40428e-05 | 0.00346711 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252656 | GGTTCCAAATGGAAA[A/T]GAAGTTTCTTCAAGA | 56916 |
rs768600720 | snp | A/G | | | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208201 | CCTTCTAATTGTTGC[A/G]GCCTAACAATGAAGC | 56916 |
rs768615672 | snp | A/G | 1.65842e-05 | 0.00287955 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226158 | CAGATAATGAAAGAA[A/G]AGCAAGTATATCATA | 56916 |
rs768637780 | in-del | -/AAAG | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238614 | CAAGACCCTGTCTCA[-/AAAG]AAAGAAAGAAAGAAA | 56916 |
rs768684401 | in-del | -/GTTA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211530 | GTGGGATAATGCTGC[-/GTTA]GTTTATTTACAGTAA | 56916 |
rs768755169 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257486 | GGGAAAGTTAAGTAA[C/T]TTACAGGATTAAGTG | 56916 |
rs768819433 | snp | A/G | 1.6517e-05 | 0.00287372 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94264823 | ATGTGAAGACATTTC[A/G]AATAAATTGACCAAA | 56916 |
rs768860849 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228106 | CTTCTGATAAGATGA[A/G]GACTTCATCTTAAAA | 56916 |
rs768905636 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216710 | AAAGTGGAATCATCA[C/G]TTAGCATAACATCCC | 56916 |
rs768925362 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222223 | CAATGGTTTGGCATA[G/T]TTTGAAATGACATGT | 56916 |
rs768936077 | snp | C/G/T | 0.000173199 | 0.00930428 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233936 | AAATGTTTTTTGCTC[C/G/T]TCTAAAAATATTTTT | 56916 |
rs768937625 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281080 | AATTAGTTTTTAAAG[A/T]CACTATTTGTTAGTT | 56916 |
rs768942719 | snp | A/T | 1.64895e-05 | 0.00287132 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94285006 | GGGACGATTGAAGAA[A/T]CCATGCTAAAAATTA | 56916 |
rs768945811 | snp | C/T | 3.33183e-05 | 0.00408143 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208354 | CCTGCAGATAGTTCA[C/T]TTAAAGCCCCCATCC | 56916 |
rs768956303 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247189 | AGTAGCCCATACATC[A/C]TGGGTCAGGGAACTG | 56916 |
rs768961200 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282638 | TATATATTTTGATTT[-/A]TTTTTTTTCTGTTGG | 56916 |
rs768988965 | snp | A/G | 1.6766e-05 | 0.00289529 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94273667 | GGCATACCTCTATCA[A/G]GAGGGTAATAATGGT | 56916 |
rs768993858 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265580 | ATCGCCCACATTTTG[C/T]ATGTTGTTGGCAGAT | 56916 |
rs769005614 | snp | C/T | 3.29647e-05 | 0.00405971 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270829 | AAATGGTAAGTGTAC[C/T]TTATTTCTAAGATTT | 56916 |
rs769008620 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218356 | TGGCATGATCTCTCT[C/T]ACTGCAACCCCCACC | 56916 |
rs769093476 | in-del | -/AAA | 1.65222e-05 | 0.00287417 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274856 | AAAGTACAGCACAAT[-/AAA]TAGTCATGTGTTTAT | 56916 |
rs769117684 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234820 | CTGCTACCACTACCA[C/G]TTCTCCTCCTCACCA | 56916 |
rs769146960 | snp | C/T | 0.000131904 | 0.00812002 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277184 | AATGCATATTTTCTC[C/T]CAAATATGTTATTTG | 56916 |
rs769147935 | in-del | -/TTC | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236556 | TCTCCTCTTTCCCCT[-/TTC]TCTCTCCATCTGACA | 56916 |
rs769149403 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210666 | GTAAGATTTTTATGC[A/G]CGGTGGCTGAAGCCT | 56916 |
rs769151356 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267407 | GTCGGACAGCATCCG[C/T]AACCTGTTTTCTATG | 56916 |
rs769183441 | snp | C/T | 1.64909e-05 | 0.00287144 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94249692 | AGAATCTAGCAGTAA[C/T]TGGGAAAAGCAGGAA | 56916 |
rs769200659 | snp | C/G | 1.65545e-05 | 0.00287697 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252975 | GCTCAGAAGATAACA[C/G]AACTCCGGCCCTTTA | 56916 |
rs769201123 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282376 | GCTGGGATTACAGGC[G/T]TGAGCCACCGCGCCC | 56916 |
rs769217404 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212505 | TATTATTATTTTTTT[A/G]AGATGGAGTCTTGCT | 56916 |
rs769219051 | snp | A/G | 3.30753e-05 | 0.00406652 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276990 | GTGGCTCTTTAAGAA[A/G]AAGCTAATATAAATT | 56916 |
rs769231297 | snp | A/G | 3.29495e-05 | 0.00405877 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208454 | TAAGATTGAGGAAGC[A/G]CCCGAAGCAACCCCT | 56916 |
rs769283642 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242776 | TTTTTAATTAGCTGG[G/T]CATGCTTACATGCAG | 56916 |
rs769293514 | in-del | -/T | 0.000115311 | 0.00759226 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240878 | TATTTCTGTGCAAAG[-/T]TTTGAGTGTGCTGCT | 56916 |
rs769338833 | in-del | -/GTTT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240285 | GCATATGTAGCTCTA[-/GTTT]GTTTTCTTCCAGTCA | 56916 |
rs769338853 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267432 | TCTATGAACTGCTTT[A/T]AACAAGTCTCTCTAG | 56916 |
rs769418111 | snp | A/G | 1.7939e-05 | 0.00299486 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281638 | AACTCATTTATTATT[A/G]TTGTTAGGATTTTAA | 56916 |
rs769433478 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231259 | TCTTGAGCACATTGC[C/T]GATTGGGGAGGAAGA | 56916 |
rs769433566 | snp | A/G | 1.64988e-05 | 0.00287213 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94236981 | AAGCACTATGGATGG[A/G]GCAATTGCTGCTGCC | 56916 |
rs769465536 | in-del | -/TA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235496 | ACATTATTTTTAATC[-/TA]TATGTTATTTTTGAC | 56916 |
rs769475400 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289199 | ACCATGAATTAGATA[C/T]GATCCAGTGTATTAC | 56916 |
rs769513272 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216351 | TTAGATTTTTATGTG[A/G]TCACCTTGTTCATCC | 56916 |
rs769516236 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218558 | TTGGCCTCCCAAAGT[A/G]TTGGGATTACCGCAC | 56916 |
rs769519516 | snp | A/T | 1.65441e-05 | 0.00287607 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94264749 | TTATCAGAAGATTTG[A/T]TATGGCACTGTAAAA | 56916 |
rs769527344 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269554 | TATGGGATTTTTAAA[C/G]GGTTAAATGAGGTGA | 56916 |
rs769527392 | snp | A/C | 1.65018e-05 | 0.00287239 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274831 | GCTTTTAACTTTGGA[A/C]ATTAAAAATAAAGTA | 56916 |
rs769604697 | snp | A/G | 1.68422e-05 | 0.00290187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234139 | TTATATTCATTGGTT[A/G]TTGTAGCTGTAATGA | 56916 |
rs769680206 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248807 | GTGCAGAGGAGGTAT[C/T]AGAATTTAGTTATTT | 56916 |
rs769704087 | snp | A/C | 4.87365e-05 | 0.00493618 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252634 | TGCAATATGTATCAC[A/C]AAGTGAGGTTCCAAA | 56916 |
rs769726151 | snp | A/G | 1.65562e-05 | 0.00287712 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94250791 | CATGAATGGATGTAC[A/G]CAGAAGCTTTAGAAT | 56916 |
rs769744643 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219417 | CCTTAATCTCCTACT[A/G]GTGATTTTTTGTTTG | 56916 |
rs769813190 | in-del | -/G | 1.65351e-05 | 0.00287528 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274875 | AGTCATGTGTTTATT[-/G]TTTTTAAATTCTAGG | 56916 |
rs769821110 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256179 | ATGCTGACCAATGCG[A/C]CATGCATCAGTAACT | 56916 |
rs769902133 | snp | G/T | | | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206815 | ATATTTAGCAGAGAC[G/T]GAGTTTCACCATGTT | 56916 |
rs769903165 | snp | A/G | 4.18953e-05 | 0.00457667 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264933 | TGAATATATTTATTC[A/G]TATTTTATCTCAATT | 56916 |
rs769929049 | snp | A/C | 0.000162641 | 0.00901633 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290071 | TGTCAGCAAGAACTC[A/C]ACCTGAATTTAAAGG | 56916 |
rs769953912 | snp | G/T | 1.67335e-05 | 0.00289248 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226131 | CAGAAGATTCTAGTG[G/T]TCCAGAAACTCCAGA | 56916 |
rs769979835 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271493 | CATGTTCAGCAAAGA[A/T]AATGTTACACTGTGT | 56916 |
rs770003437 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223457 | GAGATCACGCCACTG[A/T]ACTCTAGCCTGGGCG | 56916 |
rs770032926 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270123 | TTGCTAAAACATCAG[G/T]GAACATCAGTGAGTA | 56916 |
rs770034388 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232720 | CACTTTGGAAGGCCA[A/G]GGCGGGCGGATCGCT | 56916 |
rs770100671 | snp | A/G | 1.68451e-05 | 0.00290211 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94240943 | ATTATCTTCTTCTTC[A/G]GAGCCATATGAGGAA | 56916 |
rs770134473 | snp | A/G | 1.65693e-05 | 0.00287826 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94279011 | TCGCCAATATTACAC[A/G]GCTGAAAAACTCAAG | 56916 |
rs770136532 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290033 | CTTTCATTTTATTGC[C/T]ATTTGAAGCAGATGT | 56916 |
rs770140991 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279552 | TTACGGCAGTGACTA[C/T]TTTTATAAATAAGGT | 56916 |
rs770159607 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265423 | TCAGCAAGGGAAAGG[A/T]CAGATACTTTGATTA | 56916 |
rs770190356 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237345 | TGTCTTAGGGAAAGG[C/T]GTAGCTGGTAATCAA | 56916 |
rs770224595 | snp | C/T | 1.67531e-05 | 0.00289418 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208343 | TTTATTTTTCCCCTG[C/T]AGATAGTTCATTTAA | 56916 |
rs770242349 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94270788 | ATTGGTACATAAACA[C/T]GGACTTAATGGCATT | 56916 |
rs770272734 | in-del | -/TTAG | 0.000101261 | 0.00711478 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252586 | TTATGTATTTCTAAT[-/TTAG]TTACTGTTTTTGTCT | 56916 |
rs770284416 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287836 | ACTTTTTGAATTTTT[G/T]TATTACAGAAATAGT | 56916 |
rs770286891 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250049 | TCATCTGTAACCCTG[C/T]CCCCATCAAGTAACT | 56916 |
rs770360885 | snp | A/T | 0.000372301 | 0.0136386 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248546 | GTTTCTCCAGATGGG[A/T]TTCACCAGTATGTCT | 56916 |
rs770399512 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233846 | GATTGCATTTACTAT[C/T]GAAAAGAACTGCAGA | 56916 |
rs770451083 | in-del | -/TT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258877 | GTGTTGTGTATATTA[-/TT]AATGAAATGCCAAGA | 56916 |
rs770461642 | snp | A/G | | | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209417 | TCCTGAGCATAAACT[A/G]ATTAGTTAGTTTCTT | 56916 |
rs770492286 | snp | A/G | 1.64825e-05 | 0.00287071 | missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208438 | GCTTTGAGAAAAGGA[A/G]TAAGATTGAGGAAGC | 56916 |
rs770592722 | in-del | -/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250123 | AATTTAAAAAGTATT[-/C]CATTTCAGTGTCTTA | 56916 |
rs770621110 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210449 | TGGAAAATGGTGAAA[A/G]AAAGTTTTAAAAGTC | 56916 |
rs770642814 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288978 | GGTAATTTAAAGTGG[A/C]TAATTTAATCATCAG | 56916 |
rs770643417 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229201 | CTGGGTAATAGTCCT[A/G]TTCGCTAGCCAGCTT | 56916 |
rs770694110 | snp | C/T | 1.66513e-05 | 0.00288537 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94233961 | ATTTTTAGTTCTGAG[C/T]CATCTGAAGATGAAG | 56916 |
rs770700776 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258954 | GAATCAAACTTTCTA[A/C]AATCAAACTATTCTT | 56916 |
rs770708420 | snp | C/T | 4.94874e-05 | 0.00497406 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252941 | ACTTACTTTGATTCC[C/T]CAGTGTTCTCAGAAA | 56916 |
rs770715605 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278059 | CAAAGAAATAAAGGA[-/T]TTTTCTACCCCCCAC | 56916 |
rs770799430 | in-del | -/TATC | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285101 | AGAAACTTCAATATT[-/TATC]TATCTATATGACCAT | 56916 |
rs770801956 | snp | A/G | | | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94274905 | GTTCTCAAGAAGAAC[A/G]TAAACAAATTAGATT | 56916 |
rs770815363 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248006 | CCCACATCCTCCCTC[C/T]GCCTTCTTGTGTTCC | 56916 |
rs770817967 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218347 | GGAGTGCAGTGGCAT[A/G]ATCTCTCTCACTGCA | 56916 |
rs770844011 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227088 | GAGAAGACAGTGCTG[C/G]AGCAAAGACATAAAG | 56916 |
rs770848269 | snp | G/T | 1.64841e-05 | 0.00287085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274807 | ACTATGGTAAGAATA[G/T]GTCATTCTGCTTTTA | 56916 |
rs770864525 | snp | A/C | 1.87735e-05 | 0.00306372 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273734 | TTGTAATACTGGAGA[A/C]AACTGTATTTAACTT | 56916 |
rs770868382 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247391 | ATGAGTATATTCAGT[C/T]ACCAGGGATAAGCAG | 56916 |
rs770880772 | snp | C/T | 1.66479e-05 | 0.00288508 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280832 | CAATTACTTTAACTT[C/T]TTAAAGCAATTCTGG | 56916 |
rs770886495 | snp | A/T | 3.60991e-05 | 0.00424832 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234125 | TGATTTACTTAAGGT[A/T]ATATTCATTGGTTAT | 56916 |
rs770946034 | in-del | -/A | 0.000101858 | 0.00713573 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281615 | ATTCATGTTAGTTAC[-/A]AAAAAATAACTCATT | 56916 |
rs770973755 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221728 | CTTCCAACTCCCGTT[C/T]AGCTCTTATATGGGC | 56916 |
rs770973948 | snp | A/G | 1.64863e-05 | 0.00287104 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289556 | AACTGTGAACTCTCA[A/G]TTGATGAGGAAATAT | 56916 |
rs770997784 | snp | C/G | 1.79987e-05 | 0.00299984 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226098 | GCTCAAAATATTTTT[C/G]TCCTTTTTATTCTCT | 56916 |
rs771022843 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236590 | ACACACATACACAAA[C/T]GTGAGCATGCACACA | 56916 |
rs771031382 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281972 | TGAGCCCCGGGGGGC[A/G]GAGGTTGCAGTGAGC | 56916 |
rs771049444 | snp | C/T | | | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206523 | GGCGGGGGAGGACCC[C/T]GGTGGTCGGTGAGCA | 56916 |
rs771088396 | snp | C/T | 1.66203e-05 | 0.00288268 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94250757 | TTATTTCTAGGAACT[C/T]AGAGAAGTACTCAAG | 56916 |
rs771113021 | in-del | -/TTTATTTTATTTTATTTTA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275797 | ACATTAACATTTTCT[-/TTTATTTTATTTTATTTTA]TTTTTTTTTTTTTTT | 56916 |
rs771134014 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284442 | GACAGAGCCTCACTC[C/T]GGCTGGAGTGCAGTG | 56916 |
rs771167482 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243805 | TGGTGATATGCTATT[C/T]TTTGACATTTGTGAT | 56916 |
rs771169866 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246224 | TCCCGGGTTCAAGCA[A/T]TTCTCCCACCTCAGC | 56916 |
rs771184889 | snp | A/G | 3.3631e-05 | 0.00410053 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94283149 | GATGAGTTTAATACC[A/G]ATATGGATATCTTTG | 56916 |
rs771212467 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259307 | AGAGATTAATAACTT[C/T]ATTTAAACCTGTGAT | 56916 |
rs771215246 | snp | A/C | 1.68658e-05 | 0.0029039 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208612 | GTTAAAATTGATGTA[A/C]CATCAAGGACAGTTT | 56916 |
rs771223768 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212915 | CCAGCCTTTGGATTT[A/G]AGGGCATACACTTAA | 56916 |
rs771291420 | snp | C/G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269943 | CTTGCAAAGTGCTGG[C/G/T]ATTACGGGCATGAGC | 56916 |
rs771297342 | snp | A/G | 1.9306e-05 | 0.00310686 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289711 | TCTCCAAATACTCAC[A/G]CGTGAAATTTCAAAA | 56916 |
rs771313475 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210803 | GCCAGGCATGGTGGA[A/G]CGTGCCTGTAATCCC | 56916 |
rs771336767 | snp | C/T | 6.606e-05 | 0.00574679 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94264820 | CAAATGTGAAGACAT[C/T]TCAAATAAATTGACC | 56916 |
rs771365919 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223250 | CTGTAATCCCAGCAC[G/T]TTGGGAGGCCGAGGC | 56916 |
rs771402350 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287650 | TACTTGGTTTAACAG[A/G]CTATTGAAGTGATTC | 56916 |
rs771414110 | snp | A/C | 1.75576e-05 | 0.00296285 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240901 | GTGCTGCTCTGCTTT[A/C]AAAGGTGGTGGGCCC | 56916 |
rs771416888 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212027 | ATATGATTCATGAGA[G/T]CAGGACCTTATCTGT | 56916 |
rs771456610 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213664 | AGTTGTAAATGATAC[A/G]CATTTGATGATATTA | 56916 |
rs771461272 | snp | A/C | 3.30186e-05 | 0.00406303 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237029 | TGCAGGTATGCTTGA[A/C]TTAATTTTAAGCCAT | 56916 |
rs771470673 | snp | A/G | 1.91584e-05 | 0.00309497 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264921 | GGTAATCTTTGTTGA[A/G]TATATTTATTCGTAT | 56916 |
rs771484027 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231638 | TTTCTCCCCTTAATA[C/G]TGGTTATGTATCTGC | 56916 |
rs771494991 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277846 | CACTTAATGTACAGT[G/T]TTTTAAATGGCCTAG | 56916 |
rs771497379 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266442 | TAGTTGTTGTTGTTG[-/T]TTTTTTAAGTGCTTG | 56916 |
rs771525905 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244884 | CTCTGATAACAGCCC[C/G]TTTTTAAGTGTGTGA | 56916 |
rs771607138 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234358 | TTAATAGCGAACATA[A/G]GTTGTGAGTTTTTTT | 56916 |
rs771610520 | snp | C/T | 2.90255e-05 | 0.00380945 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208266 | GCGGGCCCTTTATTG[C/T]CTTGGGAATAAACTG | 56916 |
rs771658744 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280806 | AGAATGGCGTTTCTT[G/T]TGTATTTTCTCAATT | 56916 |
rs771695930 | in-del | -/TTTTTTTGTTTTTTT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282093 | TTACATGCAAATACG[-/TTTTTTTGTTTTTTT]TTTTTTTTTTGAGAC | 56916 |
rs771696515 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261205 | CAGCTTCACTTTGAA[C/T]ATATCCACTTAGTAT | 56916 |
rs771701839 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249116 | ATATTAATTAATCTG[G/T]TCGGTTTATACATTA | 56916 |
rs771713987 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240007 | TAGTGACACAAATAC[C/T]CTGCTTTAAAATGTT | 56916 |
rs771733108 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286750 | ATTTGTATAAATTTG[A/G]TCAGTCTAAAATTTT | 56916 |
rs771733240 | snp | C/T | 3.3605e-05 | 0.00409895 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208337 | CCTCTCTTTATTTTT[C/T]CCCTGCAGATAGTTC | 56916 |
rs771746375 | snp | C/T | | | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209375 | AGGAACTTGGTAGAG[C/T]CTGAACTCAAGTCCT | 56916 |
rs771747707 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259298 | ATTTACATGAGAGAT[G/T]AATAACTTTATTTAA | 56916 |
rs771751078 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262024 | TGTCTTTTTAAATGC[G/T]TCTAAATGTTGGTGT | 56916 |
rs771755639 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221917 | TAAATTTGAGAAGAA[A/T]TGATAGGACAAAGGG | 56916 |
rs771772667 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279684 | GCCTAAAATATGATC[C/T]GGCCCTTTACAGGAA | 56916 |
rs771786434 | snp | A/C | 0.000162668 | 0.00901706 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290614 | CCATTGTTCAATTCC[A/C]ATTCAGTGTGAGTGA | 56916 |
rs771842865 | snp | A/G | 1.65545e-05 | 0.00287697 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276975 | ATAGACATGAAAGGA[A/G]TGGCTCTTTAAGAAA | 56916 |
rs771851922 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273061 | TCCACCCACCTCAGC[A/G]TCCCCAAGTTCTGGG | 56916 |
rs771852146 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246599 | CAGACTACACTCCCA[C/T]GAAAGTGGTGGGCCT | 56916 |
rs771859487 | snp | A/G | 1.65015e-05 | 0.00287237 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94276429 | TGAGGGCCATATGCT[A/G]AAGAATATGGGCTCC | 56916 |
rs771863266 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249959 | TATAGTATCTATACT[C/G]TATCCCTAAGTCATT | 56916 |
rs771903241 | snp | A/G | 0.000181511 | 0.00952483 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270855 | GATTTGTTGTTGAAA[A/G]TGTCATTAAAAGGTA | 56916 |
rs771905131 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287693 | AATCAGAGAACCACT[A/G]CTTTAAAATAAAGAT | 56916 |
rs771917062 | in-del | -/ATTTATT | 5.1792e-05 | 0.00508855 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281628 | ACAAAAAAATAACTC[-/ATTTATT]ATTATTGTTAGGATT | 56916 |
rs771942878 | snp | A/G | 4.95413e-05 | 0.00497677 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226267 | TACAGTTCAAGAGAA[A/G]ACATTCAACAAAGAT | 56916 |
rs772001711 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272692 | TTTGTTTCTGTTTTT[G/T]TTTTTTTAAATTGCC | 56916 |
rs772009986 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258808 | TAAATGCCATCAGTT[A/G]CCTGGCTCTTTAAAA | 56916 |
rs772012183 | snp | C/T | 1.64781e-05 | 0.00287033 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94280684 | ACTTTGTAAACAGTA[C/T]CGACACATTAATAAC | 56916 |
rs772013442 | snp | G/T | | | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94274761 | TTAAGGGAAGTTAAT[G/T]TATGGTGCCCTACTT | 56916 |
rs772062027 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215809 | GCAAAAGTATGTTAT[C/T]GTTGCTTTTTCTTTA | 56916 |
rs772147125 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243318 | GCAGAAGCAGGTACC[A/G]TGAGAGTCTGAGACA | 56916 |
rs772157403 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247355 | GCTTTTGTAAAGTGT[C/G]TGTGTAACCTCCTGG | 56916 |
rs772177399 | snp | C/T | 6.59435e-05 | 0.00574172 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289553 | AAGAACTGTGAACTC[C/T]CAATTGATGAGGAAA | 56916 |
rs772204278 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267923 | GCATCTAAATATTAG[A/G]ACCAACTAGAAAAGA | 56916 |
rs772207960 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282979 | GGCTCTTCAGTGATA[C/T]AGCCAGAGGAGAAAT | 56916 |
rs772245260 | snp | C/T | 1.68015e-05 | 0.00289836 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94273679 | TCAGGAGGGTAATAA[C/T]GGTCCTCATTTGATC | 56916 |
rs772288996 | in-del | -/AG | 2.22809e-05 | 0.00333766 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289728 | GTGAAATTTCAAAAA[-/AG]AAGCCACAAATATGT | 56916 |
rs772364440 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208477 | CAACCCCTCAACCTT[C/T]CCAGCCTGGCCCTTC | 56916 |
rs772365457 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267929 | AAATATTAGAACCAA[C/G]TAGAAAAGAATATAG | 56916 |
rs772366080 | snp | A/G | 1.69622e-05 | 0.00291219 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250724 | TAATTTGAGATTTTT[A/G]ACAAAAAGATAAATG | 56916 |
rs772380134 | snp | A/G | 1.64917e-05 | 0.00287151 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277187 | GCATATTTTCTCCCA[A/G]ATATGTTATTTGTGT | 56916 |
rs772417263 | snp | A/G | | | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252711 | ACTAAAACAAAACTA[A/G]AACAGAAATTTTCAA | 56916 |
rs772420935 | snp | G/T | 6.97618e-05 | 0.00590559 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289698 | CCACTAACTGAATTC[G/T]CCAAATACTCACACG | 56916 |
rs772443938 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285654 | TAAAAATCAATATAC[-/T]TTTAATCTGTCTACA | 56916 |
rs772445739 | in-del | -/A | 0.000203049 | 0.0100739 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208318 | GTTTTCATGGCCTTT[-/A]TTTCCTCTCTTTATT | 56916 |
rs772457471 | snp | A/G | 1.64914e-05 | 0.00287149 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94249697 | CTAGCAGTAATTGGG[A/G]AAAGCAGGAAAGTAT | 56916 |
rs772525376 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243431 | CTGCTGCCAATGCTC[C/T]GTTTTAGGCTAGGTA | 56916 |
rs772557950 | snp | A/T | 1.65274e-05 | 0.00287462 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94264787 | CCAAGAAAGAGATGT[A/T]GTTATAAGGCTTATG | 56916 |
rs772570909 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213770 | TGGACTGAATTAAGA[G/T]GTGAGTTTAGGAGAA | 56916 |
rs772574173 | snp | C/T | 5.15389e-05 | 0.0050761 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264657 | AATCAGGATTGCCTT[C/T]CTCTTTCCTAGATCT | 56916 |
rs772574476 | snp | A/G | 1.66663e-05 | 0.00288667 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278531 | AGGTAATGCATATCT[A/G]CATGTTTTTTATTTT | 56916 |
rs772576232 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94253829 | TTGCTTCAACCCTTA[C/T]GTGGGCTTTTATAGC | 56916 |
rs772588240 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230651 | GACAATCAGAAATAT[C/T]TCCAGACATTGCCAA | 56916 |
rs772632721 | snp | A/G | 3.34952e-05 | 0.00409225 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208603 | AGTTACAATGTTAAA[A/G]TTGATGTAACATCAA | 56916 |
rs772672031 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212648 | CACACCACCACAGCC[A/G]GCTAATTTTTGTATT | 56916 |
rs772698064 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221483 | AAAGGCTATGAAAGT[A/G]CCCCTCCTTTCTCCA | 56916 |
rs772707804 | in-del | -/AAAA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238613 | GCAAGACCCTGTCTC[-/AAAA]GAAAGAAAGAAAGAA | 56916 |
rs772726278 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287826 | ATGACTACATACTTT[C/T]TGAATTTTTTTATTA | 56916 |
rs772755104 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218695 | TATTTAGTGTATTGT[C/T]TGTCTTTTCTAGGGT | 56916 |
rs772756601 | snp | C/T | | | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209381 | TTGGTAGAGCCTGAA[C/T]TCAAGTCCTGGCAGT | 56916 |
rs772760489 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220669 | ACTTGCCTTTTTCAC[G/T]ATATTGATATTTGCA | 56916 |
rs772777780 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238374 | GTGCCAAACTCAAAG[A/G]TCGTTGTGAAGAACT | 56916 |
rs772778426 | snp | C/G | 1.64898e-05 | 0.00287135 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94283236 | GTTGTTATACTTCAC[C/G]ATATTGACTGTAATC | 56916 |
rs772793881 | snp | A/C | 2.37116e-05 | 0.00344314 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252671 | AGAAGTTTCTTCAAG[A/C]AGTCAAAATTACCCT | 56916 |
rs772794075 | snp | A/G | 1.65029e-05 | 0.00287248 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94276434 | GCCATATGCTGAAGA[A/G]TATGGGCTCCATTCG | 56916 |
rs772847617 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94263359 | CACTGATTGTTATCT[A/G]TACTGCTGCTTATGA | 56916 |
rs772851581 | in-del | -/AA | 2.21658e-05 | 0.00332903 | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208168 | GCAATGGAAAATTTT[-/AA]AAGATACCCCCGTCC | 56916 |
rs772867116 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215975 | AGTCTGTTAGAACTG[A/C]TGTAACTACCATGAA | 56916 |
rs772903410 | snp | A/G | 4.95462e-05 | 0.00497701 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226270 | AGTTCAAGAGAAAAC[A/G]TTCAACAAAGATACA | 56916 |
rs772917673 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227965 | ATTTTTAGAATCAGG[G/T]AGATGAGAAGAAACC | 56916 |
rs772945359 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257797 | CATATCTTTATGTAA[C/T]ATAGTTATAATGCAC | 56916 |
rs773000377 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273124 | TTAGGTTATTTCCAG[C/T]GTTTGGCTATTAAGA | 56916 |
rs773018992 | snp | A/G | 0.000162668 | 0.00901706 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290615 | CATTGTTCAATTCCA[A/G]TTCAGTGTGAGTGAC | 56916 |
rs773101703 | snp | A/G | 1.64917e-05 | 0.00287151 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94249705 | AATTGGGAAAAGCAG[A/G]AAAGTATTGTACTGA | 56916 |
rs773104613 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258855 | TTCACAATAATTTGC[A/G]TTGCAAGTGTTGTGT | 56916 |
rs773107646 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235030 | TCAAATAAAGCCATA[A/T]GGCTGGATTTTTATT | 56916 |
rs773132413 | snp | G/T | 1.64914e-05 | 0.00287149 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285076 | TAGATGAAGGTGAGT[G/T]GTTTGTAAGCAGAAA | 56916 |
rs773160467 | snp | C/T | 1.64822e-05 | 0.00287068 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252931 | CAATTGGTGAACTTA[C/T]TTTGATTCCTCAGTG | 56916 |
rs773202310 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216862 | TGCCTCCACATCTTG[A/G]CTGTTTGAATTGTAT | 56916 |
rs773245351 | snp | C/T | 6.60426e-05 | 0.00574604 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270859 | TGTTGTTGAAAGTGT[C/T]ATTAAAAGGTATTCT | 56916 |
rs773327405 | in-del | -/AAGCTCTT | 1.69149e-05 | 0.00290812 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276291 | ATTTCACTAGACTCC[-/AAGCTCTT]AAAGGTATAACCTTA | 56916 |
rs773347228 | in-del | -/T | 0.025065 | 0.109107 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249632 | TCTTAAATTGTTTTC[-/T]TTTTTTTTTTCTCCC | 56916 |
rs773364484 | snp | G/T | 1.66211e-05 | 0.00288275 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249637 | AAATTGTTTTCTTTT[G/T]TTTTTCTCCCCATTA | 56916 |
rs773394388 | snp | A/T | 1.6674e-05 | 0.00288734 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278538 | GCATATCTACATGTT[A/T]TTTATTTTTATTGTT | 56916 |
rs773406769 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291153 | TGTATTAATGTATTT[G/T]CAATGATAGGCTGTT | 56916 |
rs773464420 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268036 | ATGCTGAGAAAGGAT[C/T]TGTAATTGGCAGCAG | 56916 |
rs773473258 | snp | C/T | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94277023 | ACCTTCATTCACAGG[C/T]AAATAACCGTTTGCT | 56916 |
rs773511950 | snp | A/G | 1.71658e-05 | 0.00292961 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264667 | GCCTTTCTCTTTCCT[A/G]GATCTGAACTATTCA | 56916 |
rs773545053 | snp | A/C | 3.36214e-05 | 0.00409995 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208607 | ACAATGTTAAAATTG[A/C]TGTAACATCAAGGAC | 56916 |
rs773559109 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259300 | TTACATGAGAGATTA[A/T]TAACTTTATTTAAAC | 56916 |
rs773600114 | snp | C/T | 1.64925e-05 | 0.00287158 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277189 | ATATTTTCTCCCAAA[C/T]ATGTTATTTGTGTTT | 56916 |
rs773628840 | snp | C/G | 3.29457e-05 | 0.00405854 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208478 | AACCCCTCAACCTTC[C/G]CAGCCTGGCCCTTCT | 56916 |
rs773660044 | snp | A/C | 1.66779e-05 | 0.00288768 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236910 | ACTGAAATAATTCTT[A/C]AAGTGCTGATTTAAA | 56916 |
rs773713472 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234304 | TAACTTTTTAATAGA[C/T]GAGGTTATTTATTTG | 56916 |
rs773724193 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285671 | TTAATCTGTCTACAG[C/G]GAGAGAGAAGTGCGT | 56916 |
rs773726808 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230711 | CCCCAACTTTGAGAA[C/T]CCACTGATGTGTATG | 56916 |
rs773728450 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243443 | CTCCGTTTTAGGCTA[A/G]GTAAATCAGATACCC | 56916 |
rs773757797 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211342 | TTTAGCCTGGGGTCT[A/G]GGGATTGCTGAGGAA | 56916 |
rs773779610 | snp | A/G | 1.6528e-05 | 0.00287467 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94264793 | AAGAGATGTAGTTAT[A/G]AGGCTTATGAACAAA | 56916 |
rs773823581 | snp | A/C/G | 5.41609e-05 | 0.00520361 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208245 | TCCTGAGCCACTGGC[A/C/G]TGTTTGCGGGCCCTT | 56916 |
rs773829497 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276786 | CATCTCATAAAGGTG[A/G]TACGAGGACACAAGT | 56916 |
rs773848477 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249091 | GAGACTATGTATAGC[C/T]ACAATTCTCATATTA | 56916 |
rs773871444 | snp | C/T | 5.35776e-05 | 0.00517551 | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208200 | ACCTTCTAATTGTTG[C/T]GGCCTAACAATGAAG | 56916 |
rs773886250 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231609 | AAGTATTTTAAATTA[C/T]GGACATCCCAGCATT | 56916 |
rs773889263 | snp | A/G/T | 9.04591e-05 | 0.00672478 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208265 | TGCGGGCCCTTTATT[A/G/T]CCTTGGGAATAAACT | 56916 |
rs773897798 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219623 | TTACTCCCTAGGGCC[A/G]TGGAGTCTTCCTGCA | 56916 |
rs773899601 | snp | A/C | 1.65056e-05 | 0.00287272 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274839 | CTTTGGAAATTAAAA[A/C]TAAAGTACAGCACAA | 56916 |
rs774001160 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256670 | ATCTGGTCCTTTGCT[C/T]TGTTTAACTGGTGAT | 56916 |
rs774029035 | snp | C/T | 1.64838e-05 | 0.00287083 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94281474 | TGTATTTTCACAGGG[C/T]GATAGAGTTGTGTTA | 56916 |
rs774037475 | snp | C/G | 2.4063e-05 | 0.00346856 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252657 | GTTCCAAATGGAAAA[C/G]AAGTTTCTTCAAGAA | 56916 |
rs774091522 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273429 | TAAAGTAAGTTATAG[C/T]ATCATTTGGAGATTA | 56916 |
rs774133794 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239951 | TGAAGGTTTTTTTCA[A/G]ACTTAAAATATTACA | 56916 |
rs774213888 | snp | A/G | 0.00016368 | 0.00904505 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290550 | CTCTTATCAAAATAT[A/G]TTTTACCAGTTTCCA | 56916 |
rs774221953 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211630 | ACTCTTTTTGACTAA[A/T]CCTGTTATTTTATCT | 56916 |
rs774272140 | in-del | -/TT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235230 | GGCAACCACCAATCC[-/TT]TTTTTTTTTTTTTTT | 56916 |
rs774311152 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256455 | GCAACCTCCACCTCC[C/T]GGGTTCAAGCGATTC | 56916 |
rs774326611 | snp | A/G | 1.66629e-05 | 0.00288638 | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94279069 | AGGATTTCATATTAT[A/G]TTAACACTAAGCTTT | 56916 |
rs774395233 | snp | A/G | 3.54264e-05 | 0.00420856 | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94278879 | AGTTGATATATTTCA[A/G]CAGTTATCCGCTTGG | 56916 |
rs774496200 | in-del | -/TGTT | 1.69106e-05 | 0.00290775 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276484 | ATTAATGTAAGAGAA[-/TGTT]TGTAAAGTTTTCCAA | 56916 |
rs774500270 | snp | C/G | 6.74013e-05 | 0.00580484 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283354 | GTGCCACTTTAATTT[C/G]TGTAGACCATTAGAA | 56916 |
rs774518282 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246466 | ATGAATCAAGCAGTA[C/T]ACACCCTAATGAAGT | 56916 |
rs774542369 | snp | A/T | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208464 | GAAGCGCCCGAAGCA[A/T]CCCCTCAACCTTCCC | 56916 |
rs774544673 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240321 | ACAATATGCAGATTT[C/T]CTGTTACTGCTGTAC | 56916 |
rs774563533 | in-del | -/TAA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280546 | TTCTCATCATATTAT[-/TAA]TTATTTTTATTTTGA | 56916 |
rs774606029 | snp | A/G | 2.75152e-05 | 0.00370902 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264956 | TCTCAATTATACAAA[A/G]TATCTGAATTTATTT | 56916 |
rs774613121 | snp | A/G | 1.66371e-05 | 0.00288414 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208360 | GATAGTTCATTTAAA[A/G]CCCCCATCCCTGCAA | 56916 |
rs774628924 | in-del | -/TC | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286614 | TTTTCTCCTATTCTT[-/TC]TCCTTTGTCTAATTC | 56916 |
rs774696574 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285440 | AATAAACACGTGTTC[G/T]TTCTTTTATGGGAGA | 56916 |
rs774729420 | snp | A/G | 1.64866e-05 | 0.00287106 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94285014 | TGAAGAATCCATGCT[A/G]AAAATTAACCAACAG | 56916 |
rs774748875 | snp | A/G | 6.61649e-05 | 0.00575135 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94234004 | TTCCTACCATGGCAC[A/G]TAGAAATGATGATAT | 56916 |
rs774758822 | snp | C/G | 3.31928e-05 | 0.00407373 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252986 | AACAGAACTCCGGCC[C/G]TTTAATAGTTGGGAG | 56916 |
rs774759991 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265583 | GCCCACATTTTGCAT[A/G]TTGTTGGCAGATTGG | 56916 |
rs774764407 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94209642 | TGCAAGTTATCATTA[C/G]AATAACATTTTTAAA | 56916 |
rs774785670 | snp | A/T | 1.69585e-05 | 0.00291187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249618 | ATTGTTATTGATATC[A/T]CTTAAATTGTTTTCT | 56916 |
rs774832311 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256255 | ATCAGTGTAGATCCA[A/G]TTTTCCTTGGCTGAT | 56916 |
rs774878578 | snp | C/T | 3.29788e-05 | 0.00406058 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277185 | ATGCATATTTTCTCC[C/T]AAATATGTTATTTGT | 56916 |
rs774881671 | snp | A/G | 1.65559e-05 | 0.00287709 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94233983 | AAGATGAAGAGTCCC[A/G]AGGCCTTCCTACCAT | 56916 |
rs774903930 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229543 | TATCATTTTCCTTTC[C/T]GGAACAAGGTATCCC | 56916 |
rs774982388 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289214 | CGATCCAGTGTATTA[A/C]CGTGTATTTTTATAT | 56916 |
rs775013952 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259078 | TAAGACTAACTGTTT[G/T]AGCCTCCCTTGTGAT | 56916 |
rs775036233 | snp | C/G | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94280717 | TCAGTTAGACATGGA[C/G]TTGATTTTAGATTCT | 56916 |
rs775057697 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216470 | TTATGATAAAATACA[C/T]ATAAGAAAATTTACC | 56916 |
rs775063536 | snp | C/T | 1.64909e-05 | 0.00287144 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281440 | AGTAAAACGATTTTT[C/T]CTATTTCTAATTCAT | 56916 |
rs775089592 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254594 | TTGACATGAATTTGG[A/G]GATTATGCATTACTT | 56916 |
rs775089638 | snp | C/G | 0.000180881 | 0.0095083 | intron-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94253341 | GTTTGCTAGCCTGTT[C/G]TGATCTGTTACTGCT | 56916 |
rs775143696 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275296 | TATTTTTAACTTACA[A/G]ATAAGTATCTGTAAT | 56916 |
rs775154020 | in-del | -/AAAG | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223517 | TAAATAAATAACAAT[-/AAAG]AGAGTTTTTAAGGAA | 56916 |
rs775163857 | snp | A/G | 0.00040858 | 0.0142872 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291036 | AAAAGGAGTCTTCAT[A/G]TGTTAATACTACCTC | 56916 |
rs775171714 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261647 | GACGGGGTCTCACTC[-/T]TATCACCCAGGCTGG | 56916 |
rs775179817 | snp | A/G | 3.30038e-05 | 0.00406212 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274832 | CTTTTAACTTTGGAA[A/G]TTAAAAATAAAGTAC | 56916 |
rs775205670 | snp | C/G | 1.65573e-05 | 0.00287721 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94250803 | TACACAGAAGCTTTA[C/G]AATCTCTAAAAGTGT | 56916 |
rs775211590 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236750 | AGTCAACCTGATACA[C/T]TTTAAAATATGCTTA | 56916 |
rs775218563 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248195 | GTTCTTTTTTATTAG[C/T]CTCTTACATAGCATA | 56916 |
rs775255897 | snp | A/G | 0.000154883 | 0.00879871 | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208185 | AAGATACCCCCGTCC[A/G]CCTTCTAATTGTTGC | 56916 |
rs775260494 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243776 | CTTTTTACCATGTAT[A/G]TTATCCTGTTAGGTG | 56916 |
rs775260665 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273216 | TATATTCTTAAGGGT[A/G]GAATTGCTGGGATAG | 56916 |
rs775261622 | in-del | -/GG | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279624 | TGCTTTCTCACTACA[-/GG]GGCAGAGTTGAGTAC | 56916 |
rs775287392 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218570 | AGTGTTGGGATTACC[A/G]CACCCAGACTCCTTT | 56916 |
rs775296464 | snp | A/C | 1.69275e-05 | 0.0029092 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275013 | TTTATGCAGCCCCCA[A/C]ATTTAAAAAAGAAAT | 56916 |
rs775312810 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285295 | GTTTTTGAAAAGAAT[A/G]TGTTCAAAACTCAGA | 56916 |
rs775405494 | in-del | -/A/AA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242741 | GACTCCTGTCTCTGC[-/A/AA]AAAAAAAAAAAAAAA | 56916 |
rs775415504 | snp | A/C | 1.65239e-05 | 0.00287431 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94264851 | AAACAAGTTACCATG[A/C]TTACTGGAAATGGAG | 56916 |
rs775420217 | snp | C/T | | | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206858 | CTCAAACTCCTGACC[C/T]TGTGATTCACCTGCC | 56916 |
rs775427903 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214237 | AAGAAAATATGTTTC[A/C]GGATTATTGAAAATT | 56916 |
rs775438755 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225203 | AAATGCTACAGGTTC[A/G]GTGACTTAAGAAATT | 56916 |
rs775464725 | snp | A/G | 0.000487211 | 0.0156003 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290096 | TAAAGGTGGCATTCC[A/G]TATACTAACATCCCC | 56916 |
rs775469820 | snp | C/T | 1.69919e-05 | 0.00291473 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208622 | ATGTAACATCAAGGA[C/T]AGTTTTTAAAAGATG | 56916 |
rs775473174 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219439 | TTTTGTTTGAAGGAG[A/C]CTTGATCTTGGACCA | 56916 |
rs775475567 | snp | A/C | 0.000194647 | 0.00986335 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252636 | CAATATGTATCACAA[A/C]GTGAGGTTCCAAATG | 56916 |
rs775499360 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271560 | ATATTTGTTCCCTCA[G/T]TAGCCTCTAAGAAAG | 56916 |
rs775519810 | in-del | -/AT | 0.00207576 | 0.0321492 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289873 | TATTTCTACCTCCAA[-/AT]ATATATATATATTGT | 56916 |
rs775553461 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225618 | TACACCACATATTCA[G/T]AAGAGCTAATATTTA | 56916 |
rs775596472 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226686 | AAACAGTCTGAGCTA[C/G]GCACTGTTTTATGAT | 56916 |
rs775630589 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232429 | TTTCTCAGTCACCTA[A/G]GAGGCAAGGTCAAGT | 56916 |
rs775644871 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243915 | TGCAGAGGGAATGTT[C/T]TGAGTATTAAGGAGA | 56916 |
rs775652873 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256241 | TTGTTAACATTTAGA[A/T]CAGTGTAGATCCAGT | 56916 |
rs775688962 | snp | A/G | 0.00027416 | 0.0117049 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213179 | TATAGTTAAAATAGT[A/G]TGGTGTGATAAAACC | 56916 |
rs775696214 | snp | A/G | 3.31757e-05 | 0.00407269 | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94278760 | TTTTTACTCTTTTAT[A/G]TGAAAAAGAATCTTG | 56916 |
rs775703847 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280354 | GGTTATTTTGAACCA[A/C]GTTCTAGATGTTATT | 56916 |
rs775709624 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233881 | TTGTACTATGTATAC[A/G]CATAGACACTATAAT | 56916 |
rs775747502 | in-del | -/AATA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223514 | AAATAAATAAATAAC[-/AATA]AAGAGAGTTTTTAAG | 56916 |
rs775748672 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240097 | TATGTATGTATTTGA[A/G]CTGCATAGTTAGGGC | 56916 |
rs775763711 | snp | A/G | 1.99978e-05 | 0.00316204 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208284 | TGGGAATAAACTGCT[A/G]TGGCATTGTATCGTA | 56916 |
rs775777914 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254441 | CTGTAAATACTTGCC[C/T]GAATATCTTATAGTA | 56916 |
rs775809419 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229082 | GTCCCATTATTGTTG[-/A]ACTTTGATGACTCAA | 56916 |
rs775867074 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222200 | TCTCCAGTGTTGTCA[A/G]CTCATATCAATGGTT | 56916 |
rs775878156 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245289 | GGATGCAGAAGATGT[C/T]GATGACAGTGATAAT | 56916 |
rs775894337 | snp | A/G | 2.26868e-05 | 0.00336792 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264940 | ATTTATTCGTATTTT[A/G]TCTCAATTATACAAA | 56916 |
rs775905812 | in-del | -/C | 1.69037e-05 | 0.00290716 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208322 | TTCATGGCCTTTTTT[-/C]CTCTCTTTATTTTTC | 56916 |
rs775908103 | snp | C/T | 1.66032e-05 | 0.0028812 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94276464 | GCTACCAGCACCTTA[C/T]GACAATTAATGTAAG | 56916 |
rs775913701 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220810 | ATGCCAGTATCACTT[A/G]AAGACTCTTGAAGCA | 56916 |
rs775916080 | snp | A/G | 1.67335e-05 | 0.00289248 | splice-acceptor-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208344 | TTATTTTTCCCCTGC[A/G]GATAGTTCATTTAAA | 56916 |
rs775928085 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262312 | ACCACTAATCTGTTA[C/G]CATTGAAGCCAGAAG | 56916 |
rs775942312 | snp | A/T | 1.6939e-05 | 0.00291019 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94240973 | AGATGAATTTAATGA[A/T]GATCAATCTATAAAA | 56916 |
rs775943620 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265454 | AATAGATCATATAAG[C/T]CTACATATTTCCCCA | 56916 |
rs775967100 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289031 | TTGTTTATATGTATA[C/T]AGTGTGGGTCTGAGT | 56916 |
rs775984478 | snp | A/G | | | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208670 | TCATTTTTATTCTTG[A/G]TGTCATATATATTGA | 56916 |
rs775986476 | in-del | -/A | 0.000100082 | 0.00707325 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236909 | ACTGAAATAATTCTT[-/A]AAAGTGCTGATTTAA | 56916 |
rs776042072 | in-del | -/AAAC | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238637 | AAGAAAGAAAGAAAG[-/AAAC]AAAAAACCTCCTGAA | 56916 |
rs776148870 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241340 | CTTTTAAATTTATCC[A/G]GTATTAATTGCTTAT | 56916 |
rs776167282 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273197 | AGCGCTCATATCTCA[G/T]GATTATATTCTTAAG | 56916 |
rs776212715 | snp | C/T | 1.76799e-05 | 0.00297315 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280570 | TTATTTTGAAGTATA[C/T]TGTGTTTTGTTTTGT | 56916 |
rs776223649 | snp | A/G | 1.65086e-05 | 0.00287298 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252956 | TCAGTGTTCTCAGAA[A/G]AAGGCTCAGAAGATA | 56916 |
rs776261311 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250629 | GTGTAAAAACAAGTG[C/T]AAAATAATCAGATGT | 56916 |
rs776307895 | snp | C/T | 3.30028e-05 | 0.00406205 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252811 | ACTCTGAATATGATT[C/T]AGGTTCTGATGTCGG | 56916 |
rs776349317 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240147 | AAATCTTAAACCTTT[G/T]TAGTCTTTAGCAGGT | 56916 |
rs776398506 | snp | A/G | 3.82607e-05 | 0.00437366 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234128 | TTTACTTAAGGTTAT[A/G]TTCATTGGTTATTGT | 56916 |
rs776444789 | snp | C/G/T | 3.29545e-05 | 0.00405911 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94280705 | CATTAATAACTTTCA[C/G/T]TTAGACATGGACTTG | 56916 |
rs776477531 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258969 | AAATCAAACTATTCT[C/T]CTTTTTTTGTTGTTG | 56916 |
rs776507449 | snp | A/C | 3.37986e-05 | 0.00411074 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208616 | AAATTGATGTAACAT[A/C]AAGGACAGTTTTTAA | 56916 |
rs776526328 | snp | C/T | 1.67854e-05 | 0.00289697 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94253028 | GCTTTATTCTTTTTT[C/T]CCCCTTGTATGTGTG | 56916 |
rs776563252 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225025 | AATCTGATCCATTCC[C/T]CCTAAAATATGTAAG | 56916 |
rs776565032 | snp | A/C | 1.76605e-05 | 0.00297152 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278371 | ATAATACTGTTATTG[A/C]AATAATTTAAGTGAA | 56916 |
rs776572786 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248096 | TAAGTGGGAAATGTG[A/G]TATTTGATTTTTCTG | 56916 |
rs776587306 | snp | C/G/T | 3.29702e-05 | 0.00406008 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274810 | ATGGTAAGAATATGT[C/G/T]ATTCTGCTTTTAACT | 56916 |
rs776591806 | snp | A/G | 1.6591e-05 | 0.00288015 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94250764 | TAGGAACTTAGAGAA[A/G]TACTCAAGGAACATG | 56916 |
rs776608203 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221810 | AAAGCGTACCATTTT[A/G]TTAGGTCTATATGTA | 56916 |
rs776617307 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230443 | GTACTACATTGTGTG[A/C]ACATTCCTTATTTTA | 56916 |
rs776652112 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254237 | TCAAAACTTGTTTGG[A/C]TTTGCCTGAGTGATT | 56916 |
rs776667786 | snp | C/T | 1.64953e-05 | 0.00287182 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94249717 | CAGGAAAGTATTGTA[C/T]TGAAATTGCAAAAGG | 56916 |
rs776670139 | in-del | -/GTCA | 0.0015532 | 0.0278242 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290705 | TTTAAATTTCTGCCT[-/GTCA]GTCTATATTGCTGTT | 56916 |
rs776700712 | snp | A/C/G | 4.97066e-05 | 0.0049851 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94283175 | CTTTGTGTTTCTGCT[A/C/G]TCAACAAAAGCTGGT | 56916 |
rs776752424 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223260 | AGCACTTTGGGAGGC[C/T]GAGGCAGGTGGATCA | 56916 |
rs776770382 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287664 | GGCTATTGAAGTGAT[A/T]CTGATAAAGCTAAAA | 56916 |
rs776777440 | in-del | -/GATT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246429 | AGCCATAACTGACAA[-/GATT]TCTTAAGAGGTATTT | 56916 |
rs776794994 | snp | C/T | 3.29462e-05 | 0.00405857 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208493 | CCAGCCTGGCCCTTC[C/T]TCACCAATTTCTCTT | 56916 |
rs776798349 | snp | A/G | 1.94528e-05 | 0.00311866 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264923 | TAATCTTTGTTGAAT[A/G]TATTTATTCGTATTT | 56916 |
rs776802307 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245060 | AGAGTGTTTGTGTTA[C/T]GTGTGGCAGAAAATT | 56916 |
rs776809522 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224111 | TGTGTATGATGATAA[C/T]ATGTAGGTTTCTTCA | 56916 |
rs776824904 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277884 | TATGAACCATTTTCT[A/G]TCTTCAGTTCATAAT | 56916 |
rs776828764 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237303 | TGTGGTTTTATTATA[C/G]GTTTACGAATCTTAG | 56916 |
rs776832250 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291244 | AGTTGGGTTCTTCCT[A/G]TAATGCGCTATTATG | 56916 |
rs776850281 | in-del | -/TTT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226509 | CTGGATAACAGTGAT[-/TTT]TTTTTTTTTTTTTTT | 56916 |
rs776883322 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254272 | TGTTAAAGTATTTGC[A/T]GAAGGGCTTTCTTGT | 56916 |
rs776921067 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231680 | GAACAATTCTCTAAT[A/G]TCATTTAACTTGTAC | 56916 |
rs776921117 | snp | C/G | 1.65236e-05 | 0.00287429 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237041 | TGACTTAATTTTAAG[C/G]CATGTCGATTTATTG | 56916 |
rs776948243 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213728 | ACTCAAATGTTCCTT[C/G]CTTGGACAGCTGGAG | 56916 |
rs776957049 | snp | C/T | 3.32801e-05 | 0.00407908 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278573 | AAACTTAGGTTTTTC[C/T]CTTTACTAGAATGAT | 56916 |
rs776962533 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244756 | ATGCCCCAAAACATT[-/A]AAAAAAAAAAAAAAC | 56916 |
rs777001582 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212984 | AAAGTTGTCAATGAT[G/T]GTTATTTACACATTA | 56916 |
rs777060176 | snp | C/T | 2.11477e-05 | 0.00325168 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283101 | TTAGTGAGATTTAAC[C/T]TAATTTGTTTATCTT | 56916 |
rs777069798 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276899 | TCATTTATCACAGAA[C/T]GTTAAATTATTAATA | 56916 |
rs777091126 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265018 | TAGTGGTAGGAGAGA[A/G]CCCCCAGGTTTTCTG | 56916 |
rs777098697 | snp | A/G | 2.44813e-05 | 0.00349858 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208273 | CTTTATTGCCTTGGG[A/G]ATAAACTGCTGTGGC | 56916 |
rs777188583 | snp | A/G/T | 1.68995e-05 | 0.00290679 | synonymous-codon, missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94240931 | CAGGAAAAGAAAATT[A/G/T]TCTTCTTCTTCAGAG | 56916 |
rs777188664 | snp | A/C | 0.000105469 | 0.00726107 | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208213 | TGCGGCCTAACAATG[A/C]AGCGCAGCCATAACA | 56916 |
rs777199415 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246962 | CAAAAATACCACATC[C/T]TGTAAAGCAGCTGCA | 56916 |
rs777217945 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280395 | ATATTTTAGTATGTT[A/C]TCTCTCAAACAGTAA | 56916 |
rs777220490 | snp | A/G/T | | | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290034 | TTTCATTTTATTGCT[A/G/T]TTTGAAGCAGATGTT | 56916 |
rs777221345 | snp | C/T | 1.65045e-05 | 0.00287263 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94249674 | GGAATCAAATGAGTC[C/T]GCAGAATCTAGCAGT | 56916 |
rs777221396 | snp | C/T | 1.67953e-05 | 0.00289782 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208338 | CTCTCTTTATTTTTC[C/T]CCTGCAGATAGTTCA | 56916 |
rs777225908 | snp | C/T | | | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291671 | TACTGTAGTTCCTAA[C/T]AGTTGGCATTATCGT | 56916 |
rs777241764 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239345 | ATTGTGACAGTTCCC[A/G]TTGTTTCTTTTAACC | 56916 |
rs777268438 | in-del | -/CAA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249470 | GTGATCTTAAGTCAG[-/CAA]CAATATTTTTCATCC | 56916 |
rs777294793 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94263788 | GATGGTTTTATTTTA[C/G]TTTCCTAGATTTAGT | 56916 |
rs777296744 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236678 | TAAAATAGCAAAAAC[C/G]TAGAAAATACTGTAT | 56916 |
rs777309608 | in-del | -/T | 1.83437e-05 | 0.00302845 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233925 | AATACATTAAAAATG[-/T]TTTTTTGCTCCTCTA | 56916 |
rs777309999 | in-del | -/C | 1.65228e-05 | 0.00287422 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274859 | TACAGCACAATAAAT[-/C]AGTCATGTGTTTATT | 56916 |
rs777315298 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233672 | GCATGCAATAAATGC[A/G]TGTGAGTCCTAACAA | 56916 |
rs777318913 | in-del | -/TA | 3.3631e-05 | 0.00410053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264701 | TTTTTCTTTTTATGC[-/TA]TATAGTTCACAAAGA | 56916 |
rs777387325 | snp | A/C/T | 0.000653315 | 0.0180635 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290476 | TCAAAGCAGACTGAA[A/C/T]GTGACTTCATCTAAA | 56916 |
rs777413974 | snp | C/G | 3.29755e-05 | 0.00406038 | missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208430 | CCGTTTTCGCTTTGA[C/G]AAAAGGAATAAGATT | 56916 |
rs777420119 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223135 | TACAGGTGAAAAGAT[G/T]ATTCTTCATTTTTTA | 56916 |
rs777457998 | in-del | -/TAA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240022 | TCTGCTTTAAAATGT[-/TAA]TAACATTCCATTTTT | 56916 |
rs777511972 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266938 | CATAATCTTTATTTT[A/C]AAATGTCAAAATTTA | 56916 |
rs777590255 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250501 | TGATCCTCTAGTGTT[C/G]ACAGTACTTCATAGT | 56916 |
rs777604552 | snp | A/C | 1.6552e-05 | 0.00287676 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276979 | ACATGAAAGGAGTGG[A/C]TCTTTAAGAAAAAGC | 56916 |
rs777628792 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288880 | GTGACACAAAGAGAT[A/T]TAGAAAATCTCAAAT | 56916 |
rs777629964 | snp | A/G | 1.70842e-05 | 0.00292264 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94234059 | ATTGGAAGACCTTAA[A/G]GATGCTAAACTTCAG | 56916 |
rs777634964 | in-del | -/TTA | 0.00026116 | 0.0114242 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281630 | AAAAAAATAACTCAT[-/TTA]TTATTATTGTTAGGA | 56916 |
rs777658047 | snp | A/G | 0.000217491 | 0.0104259 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276317 | GGTATAACCTTAGAG[A/G]TGTTTTTTCTTTTGG | 56916 |
rs777678120 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284479 | TCTCTGCTCACTTCA[A/G]TCTCCACCTCCCAGG | 56916 |
rs777683238 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275290 | TATTTATATTTTTAA[C/G]TTACAAATAAGTATC | 56916 |
rs777749654 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241260 | AAATGAATCATTCTT[C/T]CTTTTCTTTCACAGC | 56916 |
rs777752412 | in-del | -/TTCTA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242002 | CAAACACCGTTATCC[-/TTCTA]TTCTATTCTCAGGAT | 56916 |
rs777759937 | snp | A/G | | | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252343 | ACATCATACAGATAC[A/G]CAGCTGCCATTTGTG | 56916 |
rs777784964 | snp | A/G | 6.59467e-05 | 0.00574187 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94281552 | ACATCATCAGCATAG[A/G]TACCTCAGATTAGAT | 56916 |
rs777817951 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284905 | AAATATAGTTTACAT[-/A]TATCCAAATAACTAT | 56916 |
rs777828946 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215868 | TTTACTAGCCATTTG[A/G]ATTTTTTGTGTTTCT | 56916 |
rs777832557 | snp | A/T | 0.000179824 | 0.00948048 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252596 | CTAATTTAGTTACTG[A/T]TTTTGTCTTTTATAT | 56916 |
rs777882213 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219099 | TTACAGGTGTGAGCC[A/G]CTGTGCCTGGCCATA | 56916 |
rs777888647 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248501 | CTGGGCTGTAAAGGT[A/G]GCAGTATGAATTTTG | 56916 |
rs777904502 | in-del | -/TTTT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226508 | TCTGGATAACAGTGA[-/TTTT]TTTTTTTTTTTTTTT | 56916 |
rs777920671 | snp | A/G | 1.65993e-05 | 0.00288086 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94274950 | GATATGAAGATTACA[A/G]TGTAATTGTGACCAC | 56916 |
rs777930006 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272755 | TGCAATTTGTTGATC[A/T]TCTTCTGTTGGATAT | 56916 |
rs777945258 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254041 | CCTGATAAGTGTCTT[A/G]AAGTGGCAATAGGGG | 56916 |
rs778002631 | snp | A/C/G | 1.78814e-05 | 0.00299006 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289699 | CACTAACTGAATTCT[A/C/G]CAAATACTCACACGT | 56916 |
rs778070516 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269735 | GTGCAATGGCATGAT[C/G]TCAGCTCACTATAAC | 56916 |
rs778072848 | in-del | -/AT | 1.66369e-05 | 0.00288412 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281599 | TGAAAGGTTGGTATA[-/AT]ATTCATGTTAGTTAC | 56916 |
rs778122049 | snp | A/C | 1.68204e-05 | 0.00289999 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250733 | ATTTTTAACAAAAAG[A/C]TAAATGACTTATTTC | 56916 |
rs778146732 | snp | C/T | 0.000162588 | 0.00901486 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290018 | GTATAGATTATATAG[C/T]TTTCATTTTATTGCT | 56916 |
rs778153028 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224896 | TAATGACCTACGAGA[A/G]AATTAATGACAGCTA | 56916 |
rs778210667 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233618 | ACTTCGTCTGACATA[A/G]AGAGTATTGGTGAAA | 56916 |
rs778243245 | snp | A/C/G | 9.27556e-05 | 0.00680957 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226089 | TTTCCAGTTGCTCAA[A/C/G]ATATTTTTCTCCTTT | 56916 |
rs778305458 | snp | A/G | 1.68173e-05 | 0.00289972 | missense, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94278952 | ACAGAAATGTGCAAT[A/G]TCATGATGCAGTTGA | 56916 |
rs778325504 | snp | G/T | 1.64849e-05 | 0.00287092 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270714 | GTAATATTTGGTAAC[G/T]CTCTCTTTACCAGTT | 56916 |
rs778356263 | snp | C/T | 1.90558e-05 | 0.00308667 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240880 | ATTTCTGTGCAAAGT[C/T]TGAGTGTGCTGCTCT | 56916 |
rs778363583 | in-del | -/TGA | 1.6486e-05 | 0.00287102 | utr-variant-3-prime, nc-transcript-variant, cds-indel | SMARCAD1 | GRCh38.p7 | 4:94289558 | CTGTGAACTCTCAAT[-/TGA]TGAGGAAATATCAAC | 56916 |
rs778377710 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255898 | GTAATGTAGGTGCCT[A/G]TTGTGAGAAAACCTC | 56916 |
rs778380752 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232467 | AGGGAATATAGAGAG[A/G]CATAATGAAAATTCA | 56916 |
rs778380868 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245958 | TTTTCCCACTGGGGC[C/T]TGCCAAAGACTTCAT | 56916 |
rs778388521 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214685 | ACTGTTTAACTGTGC[A/G]AAAGAATAAAGACAT | 56916 |
rs778429817 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258910 | ACTATTTGTTGTTTT[C/G]TGTTTGTCCACTAAG | 56916 |
rs778429891 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288914 | TCCTGTAAGTGCTTA[C/T]ACTGGGGCCTCATTT | 56916 |
rs778430387 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220364 | GCAATTCTCCCACCT[C/T]AGCCTCCCTAGTAGC | 56916 |
rs778433653 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213615 | TCAATGTAGGGAAAT[G/T]ACTGTAGAGATGACA | 56916 |
rs778433807 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244638 | AAAAGATATTGTTAA[C/T]GTCAGCCTTTGAGGT | 56916 |
rs778437451 | snp | A/G | 0.000198046 | 0.00994906 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226227 | CTTCTGATAGTGAAG[A/G]TGTCGTTTCCCCAAA | 56916 |
rs778441403 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227029 | GGAATGGTTTCTAAA[C/G]AGCGTGGTCAGAAAA | 56916 |
rs778593276 | snp | A/G | 0.000602128 | 0.0173407 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241054 | TGGCTGCTTAAGGTT[A/G]GGATATGTGGAGTTT | 56916 |
rs778596482 | snp | C/T | 1.68986e-05 | 0.00290672 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208322 | TTCATGGCCTTTTTT[C/T]CTCTCTTTATTTTTC | 56916 |
rs778628187 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287659 | TAACAGGCTATTGAA[A/G]TGATTCTGATAAAGC | 56916 |
rs778643889 | in-del | -/AG | 4.94511e-05 | 0.00497223 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274801 | TCTGTTACTATGGTA[-/AG]AATATGTCATTCTGC | 56916 |
rs778680533 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94263015 | TATACAGTGAAAAGG[A/G]CATGGAATTTTTCTC | 56916 |
rs778727669 | in-del | -/AT | | | | | GRCh38.p7 | 4:94287788 | TTTGGAACTTTAAAA[-/AT]ATATATATATATTAC | 56916 |
rs778731975 | in-del | -/TT | 1.73417e-05 | 0.00294458 | | | GRCh38.p7 | 4:94278917 | TTTTACTGTGTTCTC[-/TT]TGAGTCACAGAAAAA | 56916 |
rs778735260 | snp | A/G | | | | | GRCh38.p7 | 4:94209221 | AGTTAACTATTAGAG[A/G]AATATATTTGAGCTC | 56916 |
rs778772656 | snp | A/G | 3.306e-05 | 0.00406558 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94283191 | TCAACAAAAGCTGGT[A/G]GATTAGGAATAAATC | 56916 |
rs778776190 | in-del | -/TAAC | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228931 | TTCTAAATTTGGGTT[-/TAAC]TAATGTTTCTTCATG | 56916 |
rs778777620 | snp | G/T | 1.64776e-05 | 0.00287028 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252896 | TAAAGGTAAAATTCT[G/T]CACTTCCTTCAAGAT | 56916 |
rs778806350 | snp | G/T | 0.00128783 | 0.0253428 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291211 | GTTATATCCATACTT[G/T]TATCTCTAATGAAAT | 56916 |
rs778860868 | snp | A/T | 1.67072e-05 | 0.00289021 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284953 | CATATTTTGTATTTT[A/T]TTTTAGAGAAGTACT | 56916 |
rs778866348 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262890 | ACAGTAATTTCTGTT[-/A]AAAAAAAAAAAAAAA | 56916 |
rs778882418 | snp | A/T | 1.68088e-05 | 0.00289899 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94253033 | ATTCTTTTTTTCCCC[A/T]TGTATGTGTGTGTGT | 56916 |
rs778954921 | in-del | -/T | 2.79462e-05 | 0.00373796 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289657 | AATTTCCATATTACA[-/T]TTCTCATAGTATGGA | 56916 |
rs778957077 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216758 | GTAGCATATATCAGA[A/G]TTTCCTTCCTTTTTA | 56916 |
rs778997203 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258762 | AAGTGGGGTGTAATT[A/G]TAGTGCCTGCCTATG | 56916 |
rs778999358 | snp | A/G | 3.29674e-05 | 0.00405988 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94280667 | GACTTCGAACTACAT[A/G]TACTTTGTAAACAGT | 56916 |
rs779009280 | snp | A/G | 1.66236e-05 | 0.00288297 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94234032 | TATTTCAGAACTGGA[A/G]GACCTTTCGGAATTG | 56916 |
rs779045898 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229893 | TCATTCTGTTTTCTT[C/T]TGACAGTGAGAACCC | 56916 |
rs779054305 | snp | C/T | 0.000163172 | 0.00903102 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94290919 | AAGGCAAATAAAACT[C/T]TTACAGTGATTATTT | 56916 |
rs779116643 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218014 | TTGAAAAACACTGTT[A/C]TACATCTTGTTTATT | 56916 |
rs779211521 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282919 | ATTGAAGTAAGAGTT[A/G]GTAGGGGTAGCAATA | 56916 |
rs779221526 | in-del | -/AAA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232980 | GTGGAACCCCGTCTC[-/AAA]AAAAGAAAAAACACA | 56916 |
rs779223224 | snp | C/G | | | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94205932 | CCTCCCGAGTAGGTA[C/G]GACTACAGGCGCCCG | 56916 |
rs779225667 | snp | A/G | 1.6486e-05 | 0.00287102 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289531 | AACATCAATGGGCCT[A/G]TGAAATAAGAACTGT | 56916 |
rs779226078 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272555 | TCTTATACCTATCCT[C/T]GTGGATTTTTTTCTG | 56916 |
rs779251700 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255881 | TTTTCTGCATAATAG[C/G]AGTAATGTAGGTGCC | 56916 |
rs779277903 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283858 | AAATTGTCTACCCCT[C/T]TGAAAAAGATGAGTA | 56916 |
rs779338662 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275282 | CCAAAATTATTTATA[-/T]TTTTTAACTTACAAA | 56916 |
rs779346888 | snp | A/G | 1.67657e-05 | 0.00289527 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94273668 | GCATACCTCTATCAG[A/G]AGGGTAATAATGGTC | 56916 |
rs779364014 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274531 | CATGTTGGCCAGGCT[G/T]GTATCAAACTCCTGA | 56916 |
rs779364837 | snp | A/C | 1.6531e-05 | 0.00287493 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94264770 | CACTGTAAAACACTG[A/C]TCCAAGAAAGAGATG | 56916 |
rs779384075 | snp | C/G | 1.70284e-05 | 0.00291786 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250717 | AAGTTGCTAATTTGA[C/G]ATTTTTAACAAAAAG | 56916 |
rs779402511 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236354 | CAGTATAAAAACAGT[A/G]TATTAGAATGATGTC | 56916 |
rs779426146 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212550 | GGAGTGCAGTGGCAC[A/G]ATCTCGGCTCACTGC | 56916 |
rs779436423 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272134 | GGCCTTTTCTGTGTA[-/T]TGTACACATGCCTGA | 56916 |
rs779445332 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220309 | CTGGAGTGCAATGGC[A/G]TGATCTTGGCTCGCT | 56916 |
rs779458361 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234904 | TGGTAGAGACTAGTA[C/T]ACTATAGAGTACATA | 56916 |
rs779461963 | snp | A/G | 0.000112615 | 0.00750298 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289671 | ATTTCTCATAGTATG[A/G]ACAACTTTTTGCCAC | 56916 |
rs779479393 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224805 | TCTCTCAGGGTTTAT[G/T]TCTCTCTTTCATGGG | 56916 |
rs779509525 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225787 | GAAGAGGTGGGATTG[G/T]AATCTTTTGGGCTGT | 56916 |
rs779551692 | snp | A/G | | | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94241001 | AAAAAGACAAGACTG[A/G]ATCATGTAAGTTTAC | 56916 |
rs779564159 | snp | C/T | 1.66499e-05 | 0.00288525 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94278499 | AAAGCCATTTATTCT[C/T]AGAAGAGTAAAAGAA | 56916 |
rs779591836 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286606 | TGTTGTCTTTTTCTC[C/T]TATTCTTTCTCCTTT | 56916 |
rs779664320 | snp | G/T | 1.65831e-05 | 0.00287945 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94283172 | TATCTTTGTGTTTCT[G/T]CTATCAACAAAAGCT | 56916 |
rs779712354 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291026 | TTACAGGGCTAAAAG[G/T]AGTCTTCATGTGTTA | 56916 |
rs779713180 | in-del | -/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265082 | CATTGATTTCCCCCA[-/C]CCCCAAGTAGGGTAT | 56916 |
rs779817379 | snp | A/C | 1.66624e-05 | 0.00288633 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94264893 | ATAGAACAACCTTCC[A/C]TTCTAAACCAAAGGT | 56916 |
rs779818655 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277640 | ATCCTCTTCACAAGA[A/T]AAGTTTTGTTACTTC | 56916 |
rs779823326 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218186 | GTAGGTATAAAGTCT[A/G]TTATTTAGAAGTCCC | 56916 |
rs779830089 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286304 | CCAGAGTTCCTCAGA[C/T]TCATGTTCTCCAAAG | 56916 |
rs779866416 | in-del | -/ATC | 1.65567e-05 | 0.00287716 | cds-indel, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94226168 | AAGAAAAGCAAGTAT[-/ATC]ATATTTCAAAAATCA | 56916 |
rs779891396 | snp | A/C | 3.30044e-05 | 0.00406216 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94249677 | ATCAAATGAGTCTGC[A/C]GAATCTAGCAGTAAT | 56916 |
rs779903308 | snp | G/T | 1.80328e-05 | 0.00300268 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281639 | ACTCATTTATTATTA[G/T]TGTTAGGATTTTAAT | 56916 |
rs779922197 | snp | A/G | 1.64874e-05 | 0.00287113 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94276393 | GTTTCGACGGCTGAA[A/G]CTTAATTACGCAATT | 56916 |
rs779946891 | snp | A/C | 1.78976e-05 | 0.0029914 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252755 | TGGCTTTAACAAGAA[A/C]CGTAAAAAAAATGTT | 56916 |
rs779947484 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211057 | GCGGGCTGATCAGCT[A/G]AGGTTGGAAGTTCAA | 56916 |
rs780000495 | snp | C/T | | | stop-gained, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94233982 | GAAGATGAAGAGTCC[C/T]AAGGCCTTCCTACCA | 56916 |
rs780019702 | snp | A/G | 1.84793e-05 | 0.00303963 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276518 | ATTACTGTAAAATTT[A/G]GATTACGTAATTTAA | 56916 |
rs780067804 | snp | C/T | 1.64811e-05 | 0.00287059 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252848 | ACTAGATGAGGACTA[C/T]AGTAGTGGTGAAGAA | 56916 |
rs780097416 | snp | A/G | | | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209085 | TCAGAATGCAAATGA[A/G]TAATTGGTATTCTTC | 56916 |
rs780120572 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272547 | ACCACTATTCTTATA[C/T]CTATCCTCGTGGATT | 56916 |
rs780142335 | in-del | -/TTTAA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276920 | ATTATTAATAATGGT[-/TTTAA]TTTATCTCTCCTCCC | 56916 |
rs780144414 | snp | A/T | 1.69714e-05 | 0.00291298 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208311 | CGTATATTGTTTTCA[A/T]GGCCTTTTTTCCTCT | 56916 |
rs780152619 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221663 | AAATAAATTACTTGT[G/T]GCTTGGATATATAGT | 56916 |
rs780159797 | snp | A/G | 0.000163814 | 0.00904875 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290531 | ATAGGTCATTAACTT[A/G]AAACTCTTATCAAAA | 56916 |
rs780166422 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273798 | GTAAGGGTGTGTGTC[A/G]GAGGGGTGTTGTGGT | 56916 |
rs780192562 | in-del | -/TCTT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235841 | TTTTTCTTGTAAAAA[-/TCTT]TCTAATTTTGTAATT | 56916 |
rs780258122 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228462 | ACCCAGAAATACCAA[C/T]TAACACTAGTACAGT | 56916 |
rs780272370 | snp | A/G | 7.63825e-05 | 0.00617944 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233905 | CTATAATGAAATAAC[A/G]TTAGTAATACATTAA | 56916 |
rs780386305 | snp | A/G | | | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94281498 | TGTGTTATTTAGCCA[A/G]TTTACCATGATGCTG | 56916 |
rs780395970 | snp | A/T | 1.67234e-05 | 0.00289161 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249791 | ATTTAATCAGTGTGT[A/T]CTAAGTGTTTTTATT | 56916 |
rs780452696 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257256 | TTACCTAAAATTGAA[A/G]CAGCATGTGCAGAAA | 56916 |
rs780463117 | snp | G/T | 1.65707e-05 | 0.00287838 | missense, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94279012 | CGCCAATATTACACA[G/T]CTGAAAAACTCAAGG | 56916 |
rs780500052 | snp | A/G | 3.36146e-05 | 0.00409953 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94273655 | CATTGCATTTCTGGC[A/G]TACCTCTATCAGGAG | 56916 |
rs780503560 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282775 | CATCAGAAATGTTGT[C/G]TGCCAGTAGGAGCCG | 56916 |
rs780508663 | snp | C/T | 1.64855e-05 | 0.00287097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277181 | ATAAATGCATATTTT[C/T]TCCCAAATATGTTAT | 56916 |
rs780556993 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247146 | AGAGGGACAATTCTA[C/G]GGACTTGGATTTGGT | 56916 |
rs780582888 | snp | A/G | 1.64814e-05 | 0.00287061 | missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208441 | TTGAGAAAAGGAATA[A/G]GATTGAGGAAGCGCC | 56916 |
rs780585922 | snp | A/G | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94270801 | CATGGACTTAATGGC[A/G]TTTTGGCAGATGAAA | 56916 |
rs780599843 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267095 | TAAAAGATTTCTCAC[A/C]TGTTCAGAATACAAT | 56916 |
rs780608402 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246240 | TTCTCCCACCTCAGC[C/G]TCCCGAGTAGCTGGG | 56916 |
rs780609885 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269185 | TCTGATTTAAGATGG[A/T]CATCATTCAACTACC | 56916 |
rs780612223 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258586 | TCTCTCATTTTGAGT[C/T]TCTTGTTTCTGAATT | 56916 |
rs780670826 | snp | C/T | 1.64966e-05 | 0.00287194 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94249686 | GTCTGCAGAATCTAG[C/T]AGTAATTGGGAAAAG | 56916 |
rs780687314 | snp | C/G | 1.65949e-05 | 0.00288048 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289458 | AAGCTTTTAATGCTA[C/G]TTTCTGACCTACAGG | 56916 |
rs780744771 | in-del | -/TCCTCTTTGA | 1.64787e-05 | 0.00287038 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226323 | ATAGATATATTGTAT[-/TCCTCTTTGA]TTGCATGTGTGTGAG | 56916 |
rs780766132 | in-del | -/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266416 | ATGAAATACTTAATA[-/G]ATGAGAAAAATAGTT | 56916 |
rs780767433 | snp | C/T | 1.648e-05 | 0.0028705 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274726 | GCAAATAATGTCTCT[C/T]CTGTTCCATAGATAA | 56916 |
rs780790926 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277431 | TGAAGAGCTCAGATA[C/T]ATAGTATGTGCGGAA | 56916 |
rs780838480 | in-del | -/T/TT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226388 | TTTTGGTGACTTCCC[-/T/TT]TTTTTTTTTTTTTCT | 56916 |
rs780843426 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282006 | GATCGCACCACTGCA[C/T]TGTAGCCTGGGTGAC | 56916 |
rs780906258 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260499 | CAGGCGTGCACCACC[A/G]CACCCAGTTAATTTT | 56916 |
rs780948257 | in-del | -/GAA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239891 | TTCTGTTCTTTTTAG[-/GAA]AGAATTCAGCATGTC | 56916 |
rs780952317 | snp | A/G | | | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206536 | CCCGGTGGTCGGTGA[A/G]CATGGTTAATGGGTA | 56916 |
rs780956982 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239875 | GTGCACCTGGCTTCT[C/G]TTCTGTTCTTTTTAG | 56916 |
rs780964913 | snp | A/G | 1.66896e-05 | 0.00288869 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94278427 | TTTTGCTCAGAAATC[A/G]GCAGATGAGCAAAGC | 56916 |
rs780967791 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94290958 | AAGACTGAGAACTCA[C/T]GGCTTAACCCCAGTC | 56916 |
rs781090862 | snp | C/T | 1.65023e-05 | 0.00287244 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94236969 | GATTGAATCAACAAG[C/T]ACTATGGATGGAGCA | 56916 |
rs781091875 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243296 | TTGAAGAAGGGGCAG[C/T]AGTGATGCAGAAGCA | 56916 |
rs781113342 | in-del | -/AT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257924 | TCCCCAGTTCTGTTA[-/AT]ATATGTTAATATGGT | 56916 |
rs781126328 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284667 | CGAACTGCTGGCCTC[-/A]AGCAATCCACCTGCC | 56916 |
rs781133669 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231091 | GATGTAAAAACAATA[A/G]GTTTGAGAACTCCAT | 56916 |
rs781151489 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220041 | TCTCTTTTATGGTAC[G/T]ACTTAAAAGTGCCTA | 56916 |
rs781162719 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256019 | TTTTTATTGCCAAAT[C/T]TCACACATTTGATGG | 56916 |
rs781235831 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237929 | ATTTTAAATTTTAAT[A/G]TGTATTTCCATGTCC | 56916 |
rs781237929 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249583 | TCAAGTCAAAATACA[A/G]TGATAATTGCCTTAA | 56916 |
rs781265836 | snp | A/C | 3.31082e-05 | 0.00406854 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252621 | TTATATACAGATATG[A/C]AATATGTATCACAAA | 56916 |
rs781270518 | snp | A/G | 3.33979e-05 | 0.0040863 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274990 | GAGAAATTTGGGGAG[A/G]ATGGATATTTATGCA | 56916 |
rs781275185 | snp | A/G | 6.20136e-05 | 0.00556803 | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208239 | TAACAGTCCTGAGCC[A/G]CTGGCATGTTTGCGG | 56916 |
rs781282899 | in-del | -/TC | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247935 | TGAAGTATGAATGAA[-/TC]TGTCACCCAGATAGT | 56916 |
rs781285192 | snp | A/T | 2.29218e-05 | 0.00338532 | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208164 | AAAAGCAATGGAAAA[A/T]TTTAAAAGATACCCC | 56916 |
rs781325397 | snp | C/T | 5.61298e-05 | 0.00529734 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252743 | GAAAGCACAAAATGG[C/T]TTTAACAAGAAACGT | 56916 |
rs781400419 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239243 | ATACTATGTTATTGA[G/T]ACAGGAAACTATACT | 56916 |
rs781418968 | in-del | -/TT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258481 | TGTCAGTTTCATCTC[-/TT]TTAGAAAATCAGGAA | 56916 |
rs781437797 | snp | A/G | 1.65776e-05 | 0.00287898 | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94278739 | AATAACTTGGGTATA[A/G]TCTGATTTTTACTCT | 56916 |
rs781468227 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256013 | TTGGAATTTTTATTG[A/C]CAAATTTCACACATT | 56916 |
rs781527775 | snp | A/G | 5.79206e-05 | 0.00538117 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273594 | GTTTTAAAATGTTAT[A/G]TATTGTCTTTTAAAC | 56916 |
rs781531930 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287272 | GTCTTCAGCTGTGTC[C/T]CGGGTTTCATTTAGG | 56916 |
rs781552915 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257206 | CTTTCTTCCTCCTGA[A/G]AAAAAGATTTATCAT | 56916 |
rs781559336 | snp | A/C | 1.65847e-05 | 0.0028796 | missense, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94278997 | CATCCTTTATTACAT[A/C]GCCAATATTACACAG | 56916 |
rs781573739 | snp | C/T | 8.28645e-05 | 0.00643625 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226318 | TGATTAATAGATATA[C/T]TGTATTTGCATGTGT | 56916 |
rs781625529 | snp | A/T | 0.00032515 | 0.0127464 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290054 | AAGCAGATGTTCACC[A/T]ATGTCAGCAAGAACT | 56916 |
rs781645162 | snp | A/G | 0.00148671 | 0.027224 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248504 | GGCTGTAAAGGTGGC[A/G]GTATGAATTTTGAAG | 56916 |
rs781656035 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225089 | TAATGTTGGAATTTA[A/C]CCCTTGGAGAGAAGA | 56916 |
rs781672945 | in-del | -/GTTAA | 3.34197e-05 | 0.00408763 | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94279093 | AAGCTTTAATAAGAG[-/GTTAA]GTTGTTAGGCTATAA | 56916 |
rs781696104 | snp | C/T | 0.000163145 | 0.00903029 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290462 | AAAGCTATTTCATTT[C/T]AAAGCAGACTGAATG | 56916 |
rs781708987 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279472 | GACTAAGTTCAAAAT[A/G]ATCTGGGGGACATAA | 56916 |
rs781731512 | in-del | -/TATTTATC | 0.000622606 | 0.0176328 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285098 | AAGCAGAAACTTCAA[-/TATTTATC]TATATGACCATGCAT | 56916 |
rs781754808 | snp | C/G | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94270776 | GAATTGGCTGGCATT[C/G]GTACATAAACATGGA | 56916 |
rs796084252 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220470 | CCAGATTGCTCTCGA[A/T]CTCCTGACCTCAAGT | 56916 |
rs796094621 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271860 | ATATCATAAGATTGC[A/G]TTTGCTATCAAATGA | 56916 |
rs796223417 | in-del | -/TGA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243403 | TATACCATTTCTACT[-/TGA]TGATGGGTTGCTGCT | 56916 |
rs796225931 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249082 | AGGAAAAGTGAGACT[A/T]TGTATAGCCACAATT | 56916 |
rs796247577 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277551 | GAATATCCAGAAAAT[A/G]CCTATGCTGAGAAAT | 56916 |
rs796321374 | snp | A/G | | | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252017 | CCACCATGCCTGGCT[A/G]ATTTTTATATTTTTA | 56916 |
rs796334033 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214803 | TATATGTTTGATGAA[-/T]TTTTTTTTTTTTTGC | 56916 |
rs796365439 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216233 | CAGCAAATGTCACCT[C/T]CTAATACCATTACCA | 56916 |
rs796367042 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244348 | TGGCTGTCAGACATA[A/G]CTATTAGTGTAGATA | 56916 |
rs796411380 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225645 | TTTATGGGATGCTGG[C/T]TATGTGCCAATTACT | 56916 |
rs796414892 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232926 | CAAAGGTTGCCGTGA[C/G]CCAAGATGGCACCAC | 56916 |
rs796422429 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226895 | TTTTTCTAGAGGTGG[A/G]GTCTTGCTATGTTGT | 56916 |
rs796441490 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282122 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 56916 |
rs796460483 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239377 | CAAATTGCAGTCTTA[-/A]CAGACAGTATCATCC | 56916 |
rs796488181 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229060 | AGGAGACACATGATA[C/T]CCATTTGTCCCATTA | 56916 |
rs796511343 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226863 | TCAGGGAATCGTTTC[-/T]TTTTTTTTTTTCTTG | 56916 |
rs796518576 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223449 | AATGAGCTGAGATCA[C/T]GCCACTGTACTCTAG | 56916 |
rs796549842 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267343 | TACAGACTAATATTG[-/T]GGTAGTATTTGCAGC | 56916 |
rs796554666 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247139 | TTGATTGAGAGGGAC[A/T]ATTCTAGGGACTTGG | 56916 |
rs796561456 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262848 | CAAGGACAGGGCTGT[A/G]TCTATCTCCCAGATA | 56916 |
rs796575189 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223713 | GCTGGAACTACTGGC[A/G]TGCACCACCACTCCC | 56916 |
rs796628094 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237893 | ATTTCAAACTAGGAT[A/G]TTCAAGCAAAGTGTA | 56916 |
rs796681171 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94263457 | TCCCTGTGAAAAATA[C/T]AGAGTAGTATGCAAA | 56916 |
rs796727040 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230284 | TCATACTTTCGTGTA[-/T]TTTTTTTTTTGTTTC | 56916 |
rs796728304 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262904 | TAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAAGAA | 56916 |
rs796750629 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240744 | GCAAAGAATGTTTAC[-/T]TTTTTTTTTCAATTC | 56916 |
rs796759778 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274119 | TTAGAATAAGAGAAT[A/G]TTTGTACATGTGAAT | 56916 |
rs796872733 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229814 | GTGTTTTTTTTTTTT[-/T]AATCATTTGTTTACA | 56916 |
rs796885334 | in-del | -/AG | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250595 | GAGGTGAAATTACAC[-/AG]AAAGCATTTGTAAAG | 56916 |
rs796895449 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267390 | CGGGACATAAACTTT[G/T]GGTCGGACAGCATCC | 56916 |
rs796939636 | in-del | -/TT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214281 | TTTTTTTTTTTTTTT[-/TT]GAGACAGTTTCACTC | 56916 |
rs796952038 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211490 | CTTACTTCTTTATCA[C/T]GTGGTAACTTTTCAT | 56916 |
rs796956946 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235187 | CCATTAGCAGTCACT[C/G]TCCAGTTTTGTCCCT | 56916 |