| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs2883 | snp | A/T | 0.489024 | 0.0732638 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237459 | GAGTCAGCATTTATT[A/T]AAAAACTGGACACGC | 56916 |
| rs8026 | snp | A/G | 0.499546 | 0.0150616 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291034 | CTAAAAGGAGTCTTC[A/G]TGTGTTAATACTACC | 56916 |
| rs8336 | snp | A/G | 0.476647 | 0.105504 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290459 | TCAGTCTGCTTTGAA[A/G]TGAAATAGCTTTAAG | 56916 |
| rs14696 | snp | A/C | 0.000721891 | 0.0189848 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291178 | CAACAACAATAACAA[A/C]AAAAAAAGAAACAGC | 56916 |
| rs169488 | snp | G/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219618 | TGGAATTACTCCCTA[G/T]GGCCATGGAGTCTTC | 56916 |
| rs183993 | snp | C/T | 0.497356 | 0.0912703 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208874 | CTGAATCACTGACAT[C/T]GCTCTTCCAATAGCA | 56916 |
| rs192527 | snp | G/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210735 | tgttggccaggctgg[G/T]cttgtgatctcaggt | 56916 |
| rs204755 | snp | C/G | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210788 | ctccaccatgcctgg[C/G]taatttttgtagttt | 56916 |
| rs282447 | snp | A/G | 0.488965 | 0.0734569 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220274 | tgtttttgagatgga[A/G]ttttgctttgttgcc | 56916 |
| rs282448 | snp | G/T | 0.497121 | 0.0378299 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220260 | atttattattattat[G/T]tttttgagatggagt | 56916 |
| rs282449 | snp | A/G | 0.497091 | 0.0380279 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220077 | TTTGAATTAAAAAGC[A/G]TCATTGCAGCAGGAA | 56916 |
| rs282450 | snp | C/G | 0.489083 | 0.0730708 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218447 | ACAGGCATGCATCAC[C/G]ACGCCCAGCTAATAT | 56916 |
| rs728989 | snp | C/G | 0.43655 | 0.16643 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243330 | TGCATGTGCAGATGT[C/G]TCAGACTCTCATGGT | 56916 |
| rs1352265 | snp | A/C | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262095 | TGCTGATGAGATTAC[A/C]TAAGGAAAAGCACAT | 56916 |
| rs1352266 | snp | A/G | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278025 | AAATGGCCCCAAAAG[A/G]AAGCTAGTGCAGACT | 56916 |
| rs1352267 | snp | G/T | 0 | 0 | intron-variant, utr-variant-5-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94266066 | CTACACCATCCCATA[G/T]CACCCTATAAGGGCA | 56916 |
| rs1386532 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278123 | TCATGTATCGATTAC[A/C]TAGATAACTCTCATT | 56916 |
| rs1386533 | snp | A/C | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278021 | GGCCCCAAAAGGAAG[A/C]TAGTGCAGACTGATG | 56916 |
| rs1386534 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277925 | AAGTAGAATTTTATT[A/C]TAGGATGTGAAGGAG | 56916 |
| rs1487368 | snp | C/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248132 | gctggaaaccatttc[C/T]taagcaagctaatgt | 56916 |
| rs1565062 | snp | C/T | 0.4582 | 0.138394 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261849 | gccaaggcaagagca[C/T]tgtttgagcctagga | 56916 |
| rs1906237 | snp | A/G | 0 | 0 | | | GRCh38.p7 | 4:94251757 | cctgtgaatgaaggt[A/G]acaccattattttat | 56916 |
| rs1955242 | snp | A/G | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228794 | aactaaatccactgt[A/G]aaaAAAAAATTACCA | 56916 |
| rs1955243 | snp | G/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228615 | GCAAGATATTCTTGG[G/T]GAAGGAATCAGTACC | 56916 |
| rs1955244 | snp | A/G | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228583 | TGATTTGCATTCTAA[A/G]ACATATTCCTTATTT | 56916 |
| rs2016428 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210675 | tgggattacaggctt[C/T]agccaccgcgcATAA | 56916 |
| rs2046595 | snp | G/T | 0.0581437 | 0.160285 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218624 | TAAATTTGAAATGGG[G/T]TTTTTTCCCTCATTT | 56916 |
| rs2087170 | snp | A/C | 0.499104 | 0.0211472 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241809 | GCATGCAAGTCAACA[A/C]GGTAAGACTTTCTAC | 56916 |
| rs2129596 | snp | G/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229497 | aacacaaCAGCCTGT[G/T]TGAAGAGGCCCTCAG | 56916 |
| rs2129597 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229377 | TTTGATATTTATTGT[A/G]CCACATAAATAAAAG | 56916 |
| rs2129598 | snp | A/G | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229340 | TGGGGAGAAAAAGGA[A/G]CATTACAGACTACCA | 56916 |
| rs2129601 | snp | C/G | 0 | 0 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94205842 | agatggagttgccca[C/G]gctggagtgcaatgg | 56916 |
| rs2171383 | snp | G/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229295 | GTTCTAGAACACTGG[G/T]TAGTATACCACATTT | 56916 |
| rs2220338 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262414 | GTCTGTGTTGGACAC[A/G]GAGAAACTGATAAGA | 56916 |
| rs2276910 | snp | C/T | 0.462285 | 0.132043 | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208087 | TAAGAGGAGGTTGCA[C/T]GAGGGTCAGCTCGTG | 56916 |
| rs2306802 | snp | C/T | 0.476321 | 0.106202 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94264904 | CAACAAAGATTACCT[C/T]TGGTTTAGAATGGAA | 56916 |
| rs2306803 | snp | A/G | 0.445724 | 0.155538 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240845 | AAAAATCAATTTAAT[A/G]TAAAACAAAGGCAAA | 56916 |
| rs2632387 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235733 | TTTAATACTCCATGT[G/T]TATTCTATTAGAAGC | 56916 |
| rs2632395 | snp | C/T | 0.0923359 | 0.194016 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235342 | ATCCTGCAACAGCGA[C/T]GAATCTTTTCCACTA | 56916 |
| rs2632396 | snp | A/C | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235330 | cgacgaatcttttcc[A/C]ctaggtgaaagcagc | 56916 |
| rs2632397 | snp | C/G | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234146 | TTTATCATCATTACA[C/G]CTACACTAACCAATG | 56916 |
| rs2632398 | snp | A/G | 0.0154232 | 0.0864508 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94234003 | TATCATCATTTCTAC[A/G]TGCCATGGTAGGAAG | 56916 |
| rs2632399 | snp | A/C | 0.497091 | 0.0380279 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232590 | GTAACGAGGCAAATA[A/C]ACCTCTTCCTTTATC | 56916 |
| rs2632400 | snp | A/C | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232573 | CCTCTTCCTTTATCA[A/C]TATGCCTGTCCTTCA | 56916 |
| rs2632401 | snp | C/G | 0.499137 | 0.0207489 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225904 | GTTATTTTGCAGTTT[C/G]CACTAAAGTCTTGTT | 56916 |
| rs2632405 | snp | A/C | 0.489142 | 0.0728777 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231064 | CATCTTTCGCACAAC[A/C]ACTCAGTGAAACTGT | 56916 |
| rs2632406 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230029 | attaattaataatCC[A/G]AGTGCATTGAGTGTA | 56916 |
| rs2632407 | snp | C/G | 0 | 0 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209060 | TTCTGAGGACATCCA[C/G]GAAGTCAGGTGGATG | 56916 |
| rs2632410 | snp | A/T | 0.489024 | 0.0732638 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228356 | aaagtgttcagtagt[A/T]attgtaattgctgtt | 56916 |
| rs2632411 | snp | C/T | 0.485324 | 0.0843964 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228283 | gtaattctgaaaaga[C/T]tgtgagagttgataa | 56916 |
| rs2632412 | snp | A/C | 0.372995 | 0.217652 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228168 | TTTTATCTTGGAGTA[A/C]ATTTCAGAATTAGGC | 56916 |
| rs2632413 | snp | A/C | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227632 | cctttatctcagtac[A/C]tagtaactccatcct | 56916 |
| rs2632416 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216430 | TTAACAGACATACTA[G/T]AGGAAAATATGAATG | 56916 |
| rs2632417 | snp | C/G | 0.488965 | 0.0734569 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216391 | TATAGTGTGGTAATG[C/G]GGAATGCAGAAGACT | 56916 |
| rs2632418 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216382 | GTAATGCGGAATGCA[C/G]AAGACTTATAGGAAA | 56916 |
| rs2632419 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216373 | AATGCACAAGACTTA[G/T]AGGAAAGGATGAACA | 56916 |
| rs2632420 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216207 | tgctggagggaggaa[A/G]gggtattaggtgatg | 56916 |
| rs2632421 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216093 | aaagattgtggtcta[G/T]gaatatggccctgag | 56916 |
| rs2632422 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216087 | tgtggtctatgaata[C/G/T]ggccctgagatacct | 56916 |
| rs2632423 | snp | C/T | 0.439224 | 0.163383 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214327 | TGCAGTGAGTTGAGA[C/T]TGCGCCACTGCACTC | 56916 |
| rs2664871 | snp | C/T | 0.49706 | 0.0382258 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225130 | TAATACTTTATTGAC[C/T]TGTTTTTGAACAGAC | 56916 |
| rs2664872 | snp | A/G | 0.488965 | 0.0734569 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225801 | GGAATCTTTTGGGCT[A/G]TGGTGTTCATGCTGT | 56916 |
| rs2664873 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226738 | accatccccagcttt[C/T]tttctgccctcacac | 56916 |
| rs2664874 | snp | C/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226742 | tccccagctttcttt[C/T]tgccctcacacagct | 56916 |
| rs2664875 | snp | A/C | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228446 | aacagtaatatttca[A/C]acccagaaataccaa | 56916 |
| rs2664880 | snp | A/T | 0.488965 | 0.0734569 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223026 | TGTTTTTCTCCCTTA[A/T]ACAGACTGTAGTACA | 56916 |
| rs2664881 | snp | C/T | 0.489024 | 0.0732638 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222333 | TTGTATCTCTGATAC[C/T]TACCATACTTGAAAA | 56916 |
| rs2664882 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220763 | atacattgactacta[G/T]aaccgtctagagcct | 56916 |
| rs2664883 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220753 | tactagaaccgtcta[G/T]agccttggccttgat | 56916 |
| rs2664884 | snp | G/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235755 | TTTGGCCCTTTATGT[G/T]GAATATTTTAATACT | 56916 |
| rs2664885 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235676 | CTTTAGCCCTCATGT[C/G]TACATTTGTTTCCAC | 56916 |
| rs2664886 | snp | A/C | 0.375 | 0.216506 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235659 | ACATTTGTTTCCACA[A/C]AAAAAAAAAAAAAAA | 56916 |
| rs2664887 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235337 | GCAACAGCGATGAAT[C/T]TTTTCCACTAGGTGA | 56916 |
| rs2664888 | snp | C/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235293 | CAAAATATCACATAT[C/T]TGAATCCATTTATAT | 56916 |
| rs2664889 | snp | G/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234209 | CGTAAGATATCTTTA[G/T]AAAAATGACTATCCA | 56916 |
| rs2664890 | snp | G/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234181 | CCACTACTAACTATA[G/T]CACTGAATGCAGGAG | 56916 |
| rs2664891 | snp | A/G | 0 | 0 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94233988 | GTGCCATGGTAGGAA[A/G]GCCTTGGGACTCTTC | 56916 |
| rs2664892 | snp | A/G | 0.498392 | 0.028309 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233035 | AACATGTGATGCCTA[A/G]GAACATCTAAAAGCA | 56916 |
| rs2664893 | snp | C/G | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233004 | AATTTCCAAAGAACA[C/G]AATATGTGTGttttt | 56916 |
| rs2664894 | snp | A/G | 0.489024 | 0.0732638 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232680 | CAGGTGTGAGCCACC[A/G]TGCCTAGCCAGTGTA | 56916 |
| rs2664895 | snp | A/C | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229946 | catacttgatgactg[A/C]acagattagtaaaat | 56916 |
| rs2865345 | snp | A/G | 0.478188 | 0.10213 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235414 | AAAAATAAACATGCT[A/G]TTCAAGCCAAACAAC | 56916 |
| rs2865350 | snp | A/T | 0.373196 | 0.217538 | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291662 | TTGAAACATTACTGT[A/T]GTTCCTAACAGTTGG | 56916 |
| rs2902979 | snp | C/G | 0.49703 | 0.0384237 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256723 | ATTGGCCACTTAAAG[C/G]ATGGTAATACATATT | 56916 |
| rs2902980 | snp | A/C | 0.165853 | 0.235413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256724 | TTGGCCACTTAAAGC[A/C]TGGTAATACATATTT | 56916 |
| rs2941218 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230343 | CTAAGTAAATAAAAG[A/C]ACAAATGAATATACA | 56916 |
| rs2941219 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230331 | AAGAACAAATGAATA[C/T]ACACACATGTAGTAT | 56916 |
| rs2941220 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230297 | ATCTTTTGTGTAAGA[A/C]ACAAAAAAAAAAATA | 56916 |
| rs2941221 | snp | C/G | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230270 | AATACACGAAAGTAT[C/G]ACAATGAACTAAACA | 56916 |
| rs2941222 | snp | A/C | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230242 | ACAAACTGGTTAGTT[A/C]TAAGGTTTGAATGGA | 56916 |
| rs3066293 | snp | G/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239442 | TTGTTTTGAAAGTTT[G/T]TTTTTGAATATGAAA | 56916 |
| rs3103115 | snp | C/G | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250221 | GGCCTTTTAGCAACA[C/G]GATGCGTGGCATGAG | 56916 |
| rs3103116 | snp | A/G | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249932 | TATAGTAAACAAGGT[A/G]AATAAACAACATAAA | 56916 |
| rs3103117 | snp | G/T | 0.017122 | 0.0909277 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94249682 | TCCCAATTACTGCTA[G/T]ATTCTGCAGACTCAT | 56916 |
| rs3103118 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249591 | CACTGGGCTTAAAGC[A/C/G]ATTATCATTGTGTTT | 56916 |
| rs3103119 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249579 | AGCGATTATCATTGT[A/G]TTTTGACTCGATCTG | 56916 |
| rs3103120 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246244 | taatcccagctactc[G/T]ggaggctgaggtggg | 56916 |
| rs3103121 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245556 | GTGGTAGCTCACTGT[C/G/T]CTTGTGTTATGTGTG | 56916 |
| rs3103122 | snp | G/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245162 | CCGAGTCCAAACTGT[G/T]TTTCTTAGATCAATA | 56916 |
| rs3103125 | snp | G/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94253954 | TTGCTCCCTAACTTA[G/T]GGAATAAAACTTTCT | 56916 |
| rs3103126 | snp | C/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94253941 | TATGGAATAAAACTT[C/T]CTAAAAAATTTTATA | 56916 |
| rs3103127 | snp | G/T | 0 | 0 | intron-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94253331 | GATCAGAACAGGCTA[G/T]CAAACAACTCCTTCC | 56916 |
| rs3103130 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272971 | AAAAATACAAAATTA[G/T]CCAGGCATGGTGGCG | 56916 |
| rs3103131 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272967 | ATACAAAATTAGCCA[C/G]GCATGGTGGCGCATG | 56916 |
| rs3103132 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272939 | atgtctgtgatccca[C/G]atactctggagggct | 56916 |
| rs3103133 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272932 | tgatcccacatactc[G/T]ggagggctgaggtgg | 56916 |
| rs3103134 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272903 | GGGTGGACTGCCTAA[G/T]CTCAAGAGGTCGAGG | 56916 |
| rs3103135 | snp | G/T | 0 | 0 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94274922 | ATCTACTATGAATGT[G/T]AAATCTAATTTGTTT | 56916 |
| rs3103136 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274480 | AAAATACAAAAATTA[G/T]CCAGGCATGGTGGCG | 56916 |
| rs3103137 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274448 | gcgcctgtagtccca[C/G]ctactctggaggctg | 56916 |
| rs3103138 | snp | A/G | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287409 | ACAACACAGATTGGT[A/G]ACAAAAAGCAATACA | 56916 |
| rs3103139 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229803 | gattAAAAAAAAAAA[A/C]ACCCCACACATTTTC | 56916 |
| rs3103141 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230395 | TAATAAAAATTTCTA[A/G/T]AACTGATATGATTTC | 56916 |
| rs3103142 | snp | C/G | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230377 | CTGATATGATTTCCA[C/G]GAGATATATACATAT | 56916 |
| rs3103143 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230301 | TGCTATCTTTTGTGT[A/G]AGAAACAAAAAAAAA | 56916 |
| rs3103144 | snp | A/C | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230266 | CACGAAAGTATGACA[A/C]TGAACTAAACAAACT | 56916 |
| rs3103145 | snp | C/G | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230217 | AATGGAGAAGGGACA[C/G]AAAGAGAGTAAGGGA | 56916 |
| rs3103146 | snp | G/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210384 | AAACTGAGAAGTTTA[G/T]ATTTTACATTGTAAG | 56916 |
| rs3103147 | snp | C/G | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210427 | ATTGAAGAACTTACA[C/G]AGTGAATGGAAAATG | 56916 |
| rs3103148 | snp | G/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210484 | TATCAGTAGTGACTA[G/T]TACACACTGATTGAG | 56916 |
| rs3103155 | snp | C/G | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268179 | AGGTGTTTTGATCAG[C/G]ACATGAAATGGTTTT | 56916 |
| rs3103156 | snp | C/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268083 | TAGATTTGTCTAAAT[C/T]ACAAGTAGCTTTGTT | 56916 |
| rs3103157 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266058 | TCCCATATCACCCTA[G/T]AAGGGCACAGCAAAA | 56916 |
| rs3103158 | snp | G/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264389 | TTCACAAGTAATTGT[G/T]ACTATCTCCTATCAA | 56916 |
| rs3106133 | snp | C/G | 0.497211 | 0.037236 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206882 | ACCTGCCTCAGCCCC[C/G]CAAAGTGCTGGGATT | 56916 |
| rs3106134 | snp | A/G | 0.499992 | 0.00199679 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206940 | ATTGTACATTTTTAA[A/G]TGACTAAAATAACTG | 56916 |
| rs3106135 | snp | C/T | 0.497091 | 0.0380279 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217157 | AGTTAAAAATCAACA[C/T]Gaaacccaaagtgag | 56916 |
| rs3106136 | snp | A/G | 0.499137 | 0.0207489 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232198 | GGAAATACAAGTGAT[A/G]GAAAATAAATAATGT | 56916 |
| rs3113836 | snp | C/G | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260013 | gataggtcttttaat[C/G]tgtagattcctcatc | 56916 |
| rs3113837 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260047 | ctctctctccccctt[C/G]tgtttttccagtttt | 56916 |
| rs3113838 | snp | C/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264206 | TTGAGGGGCTATACT[C/T]TGATGATAGATGTGG | 56916 |
| rs3113839 | snp | C/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264320 | TACATTTGATACTAT[C/T]ACCTTTGGTATTAGG | 56916 |
| rs3113840 | snp | A/C | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264491 | GATATATTTTACTTT[A/C]ACATAATGAGTTTGA | 56916 |
| rs3113841 | snp | A/C | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264533 | AGAATATAAAAGTGA[A/C]ACATGTAGCAACTCA | 56916 |
| rs3113842 | snp | C/T | 0 | 0 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94273656 | ATTGCATTTCTGGCA[C/T]ACCTCTATCAGGAGG | 56916 |
| rs3113843 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274441 | CGTGCCTCAGCCTCC[A/C]GAGTAGCTGGGACTA | 56916 |
| rs3113844 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274873 | ATAGTCATGTGTTTA[G/T]TGTTTTTAAATTCTA | 56916 |
| rs3113845 | snp | C/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275445 | TTAATGCTCTTGTGT[C/T]ACATTAGTTGATTTA | 56916 |
| rs3113846 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275843 | actctgtcccccagg[A/C]tagagtgcagtggcg | 56916 |
| rs3113847 | snp | G/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286381 | CTTGGGCAAGCTTTA[G/T]ACATCTTACCTGTTC | 56916 |
| rs3113848 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287114 | cgtgagccaccgcgc[C/G]tggcctctcCTTACC | 56916 |
| rs3113849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288670 | GAGGGGAGGAGGAGA[A/G]AAGTGGTTAGTTTTG | 56916 |
| rs3113850 | snp | C/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288727 | AAAATTATTCATAGT[C/T]ACAGATCTATCACAG | 56916 |
| rs3113859 | snp | C/G | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212934 | GCATACACTTAACCT[C/G]TGCCCCCTGATTTAT | 56916 |
| rs3113861 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215699 | TACACACAAATTTCA[C/G]TAGTTTGTATCAGAC | 56916 |
| rs3113862 | snp | A/G | 0.499154 | 0.0205497 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221971 | tttaggggagtcact[A/G]ggagacatatggggg | 56916 |
| rs3113863 | snp | C/G | 0.489142 | 0.0728777 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226676 | TGTTTATTGGAAACA[C/G]TCTGAGCTAGGCACT | 56916 |
| rs3113866 | snp | C/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237740 | GGATAGCTTCACATT[C/T]CTCTGTGACTACCCA | 56916 |
| rs3113867 | snp | A/C | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244958 | ATTAATTGCTGTTAT[A/C]TAAGGCAGGGTTGCA | 56916 |
| rs3113868 | snp | C/G | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245575 | GTGAGCTACAACCTT[C/G]TGTATCTGGTGTTAA | 56916 |
| rs3113869 | snp | C/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245596 | CTGGTGTTAAAAATT[C/T]CCATTCATTTTCAGA | 56916 |
| rs3113871 | snp | C/T | 0 | 0 | intron-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94253472 | CCTAAGTGTTTTATG[C/T]TTCACCACAAAAGAA | 56916 |
| rs3113872 | snp | C/G | 0 | 0 | intron-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94253565 | TGGTTAAGCAACGTG[C/G]CCATTTTATGGAGTG | 56916 |
| rs3113873 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256490 | gcctcagcctcccta[G/T]tagctgggattacag | 56916 |
| rs3733400 | snp | A/G | 0.162909 | 0.23434 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273361 | TGCAAAAAGTCTTCC[A/G]TATTAATGTGTATTG | 56916 |
| rs3834224 | in-del | -/A | 0.005997 | 0.0544292 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289627 | TATAAAAAGTTATAA[-/A]TGTTCATAAACCCCA | 56916 |
| rs4235050 | snp | A/G | 0.488965 | 0.0734569 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236005 | CCCTTCAGTTCTAGA[A/G]ATTTAAAGGTAATGT | 56916 |
| rs4331749 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248259 | ttgtggtgtgtatca[A/G]tacttcattcttttt | 56916 |
| rs4558832 | snp | A/G | 0.488905 | 0.0736498 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226891 | TTGTTTTTTCTAGAG[A/G]TGGGGTCTTGCTATG | 56916 |
| rs4693003 | snp | A/G | 0.487368 | 0.0784625 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224318 | GCAAATAGTAGTTGT[A/G]TAGTACTTGGTTGTT | 56916 |
| rs4693004 | snp | A/G | 0.49703 | 0.0384237 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247305 | ATATCCCTTGGGCCC[A/G]CTGAGACAGATACAG | 56916 |
| rs4693375 | snp | A/C | 0.49823 | 0.0296997 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212090 | CAACGACTGGCTTGT[A/C]GTAGGCCCTCAATAA | 56916 |
| rs4693376 | snp | A/G | 0.400147 | 0.19989 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236089 | TGTGAAATAGTTCTA[A/G]GCTTGCTAAGAATAT | 56916 |
| rs4693377 | snp | C/G | 0.495927 | 0.0449436 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236105 | GCTTGCTAAGAATAT[C/G]CTTTGGCTATTTTGA | 56916 |
| rs4693378 | snp | A/T | 0.489083 | 0.0730708 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247401 | TCAGTCACCAGGGAT[A/T]AGCAGAGCTGGCATA | 56916 |
| rs4693379 | snp | G/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282100 | CAAATACGttttttt[G/T]ttttttttttttttt | 56916 |
| rs4693380 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282104 | TACGtttttttgttt[G/T]tttttttttttttga | 56916 |
| rs4693381 | snp | A/T | 0.488905 | 0.0736498 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285704 | GATCAAATAATTACT[A/T]GTCTTTCTTGCGTAG | 56916 |
| rs5860358 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210930 | AGAGACTGTATCTCA[-/A]AAAAAAAAAAAAAAA | 56916 |
| rs5860359 | in-del | -/A | 0.00716266 | 0.059414 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239376 | ACAAATTGCAGTCTT[-/A]ACAGACAGTATCATC | 56916 |
| rs5860360 | in-del | -/TT | 0.00517822 | 0.0506191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239438 | TGTTTGTTTTGAAAG[-/TT]TTTGTTTTTGAATAT | 56916 |
| rs5860361 | in-del | -/T/TT/TTT/TTTTTTTTTTTTTTTTTATTT | 0.495855 | 0.045338 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239562 | TTTTTTTTTTTTTTT[lengthTooLong]AATTTTTTATTTTGA | 56916 |
| rs6532474 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267543 | TTGAAAATAATTTTG[A/G]AACTAGTTTCTCTGG | 56916 |
| rs6532476 | snp | A/C | 0.489083 | 0.0730708 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271310 | TTTTATTTTTATTAG[A/C]GGTCTCTCCGGGTCT | 56916 |
| rs6811367 | snp | A/G | 0.160938 | 0.233598 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221986 | aggagacatatgggg[A/G]gtgtaaaactggtgg | 56916 |
| rs6817118 | snp | A/G | 0.16028 | 0.233346 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275661 | AAGTTTTAAAGAGAA[A/G]CATGTTTTAGCTTCA | 56916 |
| rs6817795 | snp | A/T | 0.496517 | 0.0415876 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206565 | tacgaaaatacagtt[A/T]gaatgaataagatct | 56916 |
| rs6823404 | snp | C/T | 0.484084 | 0.0877769 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94276369 | CAGCAGTTCTGATGA[C/T]CGTAGTCTGTTTCGA | 56916 |
| rs6826410 | snp | A/T | 0.0236746 | 0.106192 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271972 | ttgccataacaaaat[A/T]ccacagaccaagtgg | 56916 |
| rs6830123 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287927 | ggagacaggcgggag[A/G]atcgtttgagcccag | 56916 |
| rs6841961 | snp | A/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282447 | TTTATGGTTTTCACC[A/T]TTAAATTTTTTTCAA | 56916 |
| rs6844517 | snp | C/T | 0.159951 | 0.233219 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249484 | AGCAATATTTTTCAT[C/T]CTTAAAGACATAAAT | 56916 |
| rs6852926 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268162 | AAATATTTCAATGTA[A/G]TAAAACCATTTCATG | 56916 |
| rs7356258 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271702 | CTTACAGAAATTACC[A/G]AATATATGTCATTTC | 56916 |
| rs7435106 | snp | A/T | 0.496999 | 0.0386216 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248621 | AACCTTAGGCTTTAT[A/T]CCATGTTAGCTCTGG | 56916 |
| rs7439869 | snp | C/T | 0.425444 | 0.178099 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252628 | CAGATATGCAATATG[C/T]ATCACAAAGTGAGGT | 56916 |
| rs7442254 | snp | A/G | 0.496314 | 0.0427728 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256466 | CTCCCGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 56916 |
| rs7653910 | snp | C/G | 0.159951 | 0.233219 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274508 | TTTTAGTGGAGATGG[C/G]GTTTCACCATGTTGG | 56916 |
| rs7654621 | snp | C/T | 0.16028 | 0.233346 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94205702 | atgcctggataactt[C/T]gtattttttttagag | 56916 |
| rs7654919 | snp | C/T | 0.492775 | 0.059668 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215013 | GGGTCTTACAGTCTT[C/T]TCCTGGCTTTGCTTA | 56916 |
| rs7657789 | snp | C/T | 0.489142 | 0.0728777 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257438 | TAGATCCCACATTTA[C/T]AGGGTACTTTGTATT | 56916 |
| rs7659733 | snp | C/G | 0.0520825 | 0.152737 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252259 | GTAAGCTTTATAGTA[C/G]TGTAAGCATCATTCT | 56916 |
| rs7660243 | snp | A/T | 0.160609 | 0.233472 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222714 | acacctgtaatccca[A/T]catttcaggaggccg | 56916 |
| rs7661682 | snp | A/C | 0.160609 | 0.233472 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216112 | accacaatcttttaa[A/C]cccatgtggctgaat | 56916 |
| rs7684494 | snp | A/G | 0.139225 | 0.224118 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261649 | ACGGGGTCTCACTCT[A/G]TCACCCAGGCTGGAA | 56916 |
| rs7685121 | snp | A/G | 0.489142 | 0.0728777 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254531 | AGCAACTTAACATGT[A/G]GAAAGCATATTTCCC | 56916 |
| rs7688784 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258283 | cctcaccctcctgag[A/T]agttgggattacagg | 56916 |
| rs7689412 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228503 | aatatacttttcata[C/T]ttcaattttgccagt | 56916 |
| rs7697827 | snp | A/G | 0.400682 | 0.199487 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94263597 | ACTGTATTTTATTTA[A/G]TTATCTTAGTATATC | 56916 |
| rs9307136 | snp | A/T | 0.498206 | 0.0298983 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212725 | ctcctgacttcaggc[A/T]atctgcctgccttgg | 56916 |
| rs9307137 | snp | C/T | 0.429987 | 0.173507 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214561 | atgagccaccgcacc[C/T]ggccAAGCGTTTGTT | 56916 |
| rs9307138 | snp | C/G | 0.160609 | 0.233472 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288151 | TTATTTTCAATATCA[C/G]AGCATATTCCTCAAA | 56916 |
| rs9917887 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287479 | CCTCTCAAATATGCT[G/T]ATCAGATTTTTGTGT | 56916 |
| rs9991214 | snp | A/T | 0.171704 | 0.237423 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236684 | AGCAAAAACCTAGAA[A/T]ATACTGTATATATGT | 56916 |
| rs9992255 | snp | A/T | 0.16028 | 0.233346 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231791 | ACTGTGTTAATCTAG[A/T]ATGGGCCACTCCCCT | 56916 |
| rs9993132 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219409 | CGAATGAGCCTTAAT[C/T]TCCTACTAGTGATTT | 56916 |
| rs9999328 | snp | G/T | 0.160609 | 0.233472 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218037 | TGTTTATTTTTGTGC[G/T]CTTGCTTTATTAAGA | 56916 |
| rs9999656 | snp | C/T | 0.161267 | 0.233723 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272582 | tctggttatgtagta[C/T]atgcagtatactcta | 56916 |
| rs10000247 | snp | C/G | 0.48995 | 0.0701706 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252099 | TTGTGATCTGCCCGC[C/G]TCGGCCTCCCAAAGT | 56916 |
| rs10003038 | snp | C/T | 0.159951 | 0.233219 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243824 | GACATTTGTGATCTT[C/T]TCTATTTGAAAAAAG | 56916 |
| rs10007463 | snp | A/G | 0.118584 | 0.212673 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234568 | AGTAGCACTCTTGCT[A/G]AGAAATATTGATTTA | 56916 |
| rs10011076 | snp | A/G | 0.0733688 | 0.176922 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94205849 | gttgcccaggctgga[A/G]tgcaatggcgtgatc | 56916 |
| rs10011936 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282103 | ATACGTTTTTTTGTT[G/T]TTTTTTTTTTTTTTG | 56916 |
| rs10013456 | snp | A/G | 0.145305 | 0.227022 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213541 | TCTTATTTGGTACAC[A/G]TCATAGAGCATTTCA | 56916 |
| rs10014718 | snp | C/T | 0.16028 | 0.233346 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231630 | TCCCAGCATTTCTCC[C/T]CTTAATACTGGTTAT | 56916 |
| rs10016806 | snp | G/T | 0.489024 | 0.0732638 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237344 | ATGTCTTAGGGAAAG[G/T]CGTAGCTGGTAATCA | 56916 |
| rs10016925 | snp | C/T | 0.16028 | 0.233346 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237574 | AGCAAACCCACACTT[C/T]ATTAACCACCCTTAA | 56916 |
| rs10018599 | snp | A/G | 0.16028 | 0.233346 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250366 | ATTCTGATGAGCTGA[A/G]TGCAAAATCTTGTTG | 56916 |
| rs10022350 | snp | C/T | 0.159951 | 0.233219 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265637 | TCCTTTAAAAGTTTG[C/T]ATATTTTTAAGTAGT | 56916 |
| rs10022504 | snp | A/G | 0.160938 | 0.233598 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214556 | caggcatgagccacc[A/G]cacctggccAAGCGT | 56916 |
| rs10024642 | snp | A/G | 0.40086 | 0.199352 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258144 | ttgcctaaatttccc[A/G]tcagatttttttttt | 56916 |
| rs10025333 | snp | A/G | 0.171057 | 0.237209 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245335 | GTGTATGCCATGACA[A/G]TGTAATACAAATGAT | 56916 |
| rs10025839 | snp | C/T | 0.171057 | 0.237209 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245978 | AAAGACTTCATACAA[C/T]ATCCTTACCTGCAAC | 56916 |
| rs10027578 | snp | A/G | 0.139903 | 0.224452 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286287 | TCTCTTCTATGACAA[A/G]TCCAGAGTTCCTCAG | 56916 |
| rs10029551 | snp | A/G | 0.228694 | 0.24909 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264703 | TTTTCTTTTTATGCT[A/G]TAGTTCACAAAGATG | 56916 |
| rs10030586 | snp | A/C | 0.488302 | 0.0755777 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229654 | ATGATACTTGGAAAT[A/C]TAGAAACTTCTTCTG | 56916 |
| rs10030605 | snp | A/G | 0.139903 | 0.224452 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259786 | AAGCACATCTCAGAC[A/G]TCATTTTATCCTTAT | 56916 |
| rs10032125 | snp | C/T | 0.171704 | 0.237423 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248115 | TTGATTTTTCTGATT[C/T]CACATTAGCTTGCTT | 56916 |
| rs10034781 | snp | G/T | 0.471198 | 0.116496 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248531 | GAAGATTTTGAAATG[G/T]TTTCTCCAGATGGGT | 56916 |
| rs10213096 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230529 | atttattgacatttg[A/G]agccagataattctt | 56916 |
| rs10433970 | snp | C/G | 0.491481 | 0.0647075 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213014 | ATTTCTCCTTTTTTT[C/G]TTTGACTTTTGGGAG | 56916 |
| rs10516948 | snp | A/C | 0.161267 | 0.233723 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247456 | CACATGATAGGCACA[A/C]CATCTACTAAATATT | 56916 |
| rs10633066 | in-del | -/AGCC | 0.489083 | 0.0730708 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232836 | AAAAAACACAAAAAT[-/AGCC]AGGTGTGGTGGCAAG | 56916 |
| rs10640840 | in-del | -/CTAAAA | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267083 | TTTATCAGCCTTAAA[-/CTAAAA]AGATTTCTCACATGT | 56916 |
| rs11097406 | snp | C/T | 0.486398 | 0.0813386 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224891 | CTTGATAATGACCTA[C/T]GAGAGAATTAATGAC | 56916 |
| rs11097407 | snp | C/G | 0.486398 | 0.0813386 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224984 | CCTAGACCAGGCACT[C/G]TGTTTACTTTAATAC | 56916 |
| rs11097408 | snp | C/T | 0.4582 | 0.138394 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244511 | AAGACAGAAAACATG[C/T]TCTAGGATTTAAGGC | 56916 |
| rs11097409 | snp | A/C | 0.49706 | 0.0382258 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247364 | AAGTGTCTGTGTAAC[A/C]TCCTGGACCACATGA | 56916 |
| rs11097410 | snp | A/T | 0.49706 | 0.0382258 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247365 | AGTGTCTGTGTAACC[A/T]CCTGGACCACATGAG | 56916 |
| rs11418046 | in-del | -/TT | 0.494651 | 0.0514399 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214266 | TTGAGCGTTCTTTTG[-/TT]TTTTTTTTTTTTTTT | 56916 |
| rs11541128 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290119 | GCAGAAGTACTTGAG[A/T]GGACCTGGGGGATGT | 56916 |
| rs11541129 | snp | A/G | 0 | 0 | missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208543 | CTGAAGGGGAAGTTA[A/G]CAGGGCAAACACTCC | 56916 |
| rs11722476 | snp | A/G | 0.496123 | 0.043859 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94249688 | CTGCAGAATCTAGCA[A/G]TAATTGGGAAAAGCA | 56916 |
| rs11723410 | snp | C/T | 0.00632905 | 0.0558969 | missense, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226125 | CTCTTGCAGAAGATT[C/T]TAGTGTTCCAGAAAC | 56916 |
| rs11730135 | snp | A/G | 0.031825 | 0.122064 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261268 | GTGACTTACATGTTA[A/G]GAATCTTCACAGTAC | 56916 |
| rs11931108 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211124 | ctaaaaatataaaat[C/T]agctgggcatggtgg | 56916 |
| rs11933631 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221677 | tggcttggatatata[A/G]ttttcatgaagatgt | 56916 |
| rs11934625 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218859 | ctctgtcacccaggc[A/T]ggagtgtggtggtgg | 56916 |
| rs11940315 | snp | C/T | 0.00468381 | 0.0481661 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207308 | TATACACTGAAAAAG[C/T]TTAGCACAGTATTAT | 56916 |
| rs11943926 | snp | A/G | 0.49823 | 0.0296997 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215361 | CAGTGGCTCATGCCT[A/G]TAGAGTCGCAGCACT | 56916 |
| rs11944297 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231519 | TATATAAAGAACACC[C/T]GTATACCTTCCACCT | 56916 |
| rs11944408 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210767 | agtgaaaccccgtct[C/T]tactaaaaatacaaa | 56916 |
| rs11946179 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229956 | tctgttcagtcatca[A/G]gtatgcataaaatag | 56916 |
| rs11947059 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212730 | gacttcaggctatct[A/G]cctgccttggcctcc | 56916 |
| rs12172983 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206201 | cattctcatgtttgt[G/T]gcagcactattcaca | 56916 |
| rs12186176 | snp | C/T | 0.139225 | 0.224118 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227657 | taaaggtgactgttt[C/T]tgctgtgggtgggca | 56916 |
| rs12499309 | snp | A/G | 0.499137 | 0.0207489 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250133 | GTATTCCATTTCAGT[A/G]TCTTAATATTTTATA | 56916 |
| rs12511433 | snp | A/G | 0.458084 | 0.138567 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241274 | TTCTTTTCTTTCACA[A/G]CTAAGCCAGATAATT | 56916 |
| rs12643901 | snp | C/T | 0.49706 | 0.0382258 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223981 | TAATACAGTAAAGAT[C/T]TAAATTTTTAGTTTT | 56916 |
| rs12645192 | snp | C/T | 0.49703 | 0.0384237 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260374 | tttgagacagtctct[C/T]gctctgtcactcagg | 56916 |
| rs12645998 | snp | A/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254146 | ATATTCCATAGCTTT[A/T]AAAAATAATAATAAA | 56916 |
| rs12646184 | snp | C/T | 0.49706 | 0.0382258 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262065 | TTTGCTCTCAGTCTT[C/T]TAATCTCCAATTTCA | 56916 |
| rs12647120 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226066 | ATTATAACTAACAAC[A/T]GATTCGTTTTCCAGT | 56916 |
| rs13102349 | snp | A/T | 0.0444908 | 0.142359 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236362 | AAACAGTATATTAGA[A/T]TGATGTCATGCAAGC | 56916 |
| rs13103548 | snp | G/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257769 | ctttttgtctcattg[G/T]tctgatcacctccat | 56916 |
| rs13104332 | snp | A/C | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261373 | CTAACCTTCAACAAT[A/C]CAGTAACATCTTTAG | 56916 |
| rs13108619 | snp | A/G | 0.49703 | 0.0384237 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279923 | AGGCTGGAGTGCGAT[A/G]GCATGATCTCTGCTC | 56916 |
| rs13112528 | snp | G/T | 0.497091 | 0.0380279 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287070 | GGGGTTTCACCGTAT[G/T]AGCCAGGATGGTCTT | 56916 |
| rs13112644 | snp | C/G | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232430 | ttctcagtcacctaa[C/G]aggcaaggtcaagta | 56916 |
| rs13120541 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284197 | ccaggcgtggtggca[G/T]gcgcctgtagtccca | 56916 |
| rs13131414 | snp | A/G | 0.185788 | 0.241613 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275959 | cccaccaccacaccc[A/G]gctaattttttatat | 56916 |
| rs13135767 | snp | C/T | 0.480539 | 0.0967035 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279922 | CAGGCTGGAGTGCGA[C/T]GGCATGATCTCTGCT | 56916 |
| rs13135934 | snp | C/G | 0.49703 | 0.0384237 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286537 | TATTATCGAAAATCA[C/G]TTTCCATTCTTTCAT | 56916 |
| rs13142645 | snp | A/G | 0.499598 | 0.0141716 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287563 | CCTAAGAAATTGGCA[A/G]TTTGAAATGCAAATT | 56916 |
| rs13148156 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243028 | cccaggcatgatctc[A/G]gctcactgaaacctc | 56916 |
| rs13434570 | snp | C/T | 0.489142 | 0.0728777 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246868 | GATAAAAACGGATTG[C/T]TTCTGTTTGATCTAA | 56916 |
| rs13435702 | snp | A/G | 0.478354 | 0.101757 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246600 | AGACTACACTCCCAC[A/G]AAAGTGGTGGGCCTC | 56916 |
| rs17021401 | snp | A/G | 0.135143 | 0.222054 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232281 | TATTTATTACATCAT[A/G]AGGCACATGAATTTG | 56916 |
| rs17303283 | snp | C/T | 0.159951 | 0.233219 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231262 | TGAGCACATTGCCGA[C/T]TGGGGAGGAAGAGCT | 56916 |
| rs17303457 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232601 | AGGTGTATTTGCCTC[A/G]TTACTTTAGAGCGGT | 56916 |
| rs17309887 | snp | C/T | 0.314301 | 0.241589 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234354 | AGCCTTAATAGCGAA[C/T]ATAGGTTGTGAGTTT | 56916 |
| rs17310266 | snp | C/T | 0.497091 | 0.0380279 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255900 | AATGTAGGTGCCTAT[C/T]GTGAGAAAACCTCAT | 56916 |
| rs17374902 | snp | C/T | 0.160938 | 0.233598 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207526 | GGAGACGGGTACGAA[C/T]TACCATGACAACAGC | 56916 |
| rs17374964 | snp | A/C | 0.16028 | 0.233346 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209013 | AGACAACCTCTGTAC[A/C]CAAGGGAAGATCAGA | 56916 |
| rs17376278 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268268 | GTTTTTTAAATTTCC[G/T]CATCACTTTTTAAAA | 56916 |
| rs17854344 | snp | A/C | 0 | 0 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252778 | AAAATGTTTTTAATC[A/C]AAAGAGAGTTGTTGA | 56916 |
| rs17857297 | snp | C/T | 0 | 0 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94284965 | TTTTTTTTAGAGAAG[C/T]ACTAGTTATAAAACT | 56916 |
| rs28374259 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228535 | ATACCAGTAATGTCC[G/T]TTAGAGCATTGCTAC | 56916 |
| rs28379069 | snp | A/G | 0.160609 | 0.233472 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219002 | TTTTTAGTAGGGACA[A/G]GGTTTCACCATGTTG | 56916 |
| rs28442028 | snp | A/G | 0.170084 | 0.236883 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215993 | TAACTACCATGAACC[A/G]GGTAGCTTATAAGCA | 56916 |
| rs28470897 | snp | C/G | 0.16028 | 0.233346 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228918 | TTTTTTAGAATTTTT[C/G]TAAATTTGGGTTTAA | 56916 |
| rs28491758 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290250 | TCCAACTGCACTAAT[A/T]GTGCATATTACTCTG | 56916 |
| rs28497628 | snp | G/T | 0.0689305 | 0.172377 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247827 | AATTTCAGAAAAATG[G/T]GTTTTATTTGTTTTT | 56916 |
| rs28508095 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240900 | TGTGCTGCTCTGCTT[A/T]AAAAGGTGGTGGGCC | 56916 |
| rs28522293 | snp | A/G | 0.480302 | 0.0972668 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245936 | TCTTTAAAACTCTCT[A/G]AAACGATTTTCCCAC | 56916 |
| rs28525661 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228454 | TATTTCAAACCCAGA[A/G]ATACCAATTAACACT | 56916 |
| rs28539776 | snp | A/T | 0.0566069 | 0.158427 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276641 | GTAAATATTTCACAC[A/T]TTATGGACTAGATGG | 56916 |
| rs28544271 | snp | C/T | 0.138886 | 0.22395 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217781 | AAACTGGATCATAAA[C/T]ATTTATTGTGTCATA | 56916 |
| rs28548547 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275627 | TCTTGGATCTAATCT[A/G]CTAGTTTAATAAAAT | 56916 |
| rs28573143 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248244 | CAATGTTCATTCATG[C/T]TGTGGTGTGTATCAG | 56916 |
| rs28592662 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284052 | GATAGCCGGGCACGG[G/T]GGCTCACACCTGTAA | 56916 |
| rs28627334 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250257 | TTTAATCCCATGATC[A/G]TATATAGAAGCACAT | 56916 |
| rs28638427 | snp | C/T | 0.159951 | 0.233219 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217824 | TGGGTCCTGACTAAA[C/T]ATGTATAACTACAAT | 56916 |
| rs28649197 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228903 | GATAATAGGCCAGGT[G/T]TTTTTAGAATTTTTC | 56916 |
| rs28659924 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214355 | GCAATCTCTGCTCTC[A/G]GGTTCATGCCATTCT | 56916 |
| rs28676794 | snp | A/G | 0.160609 | 0.233472 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254719 | TGTAACAGTCTAAAT[A/G]TATCTGAAAAGTAAA | 56916 |
| rs28696050 | snp | C/G | 0.486332 | 0.08153 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215479 | TGAAAAAATTAGTCA[C/G]GTGTGGTGGTGTGCA | 56916 |
| rs28701470 | snp | A/C | 0.480144 | 0.097642 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245937 | CTTTAAAACTCTCTA[A/C]AACGATTTTCCCACT | 56916 |
| rs28733161 | snp | C/T | 0.17138 | 0.237316 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254718 | ATGTAACAGTCTAAA[C/T]GTATCTGAAAAGTAA | 56916 |
| rs28735979 | snp | A/T | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223761 | TTTTTTTTTTTTTTT[A/T]AAGTAGAGACGAGGT | 56916 |
| rs33970526 | in-del | -/A | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262913 | AAAAAAAAAAGAAAG[-/A]AAAGAAATGGTAGTT | 56916 |
| rs34021113 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229657 | ATACTTGGAAATATA[G/T]AAACTTCTTCTGTGT | 56916 |
| rs34130722 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211133 | AAAATTAGCTGGGCA[-/T]TGGTGGTACATGCCT | 56916 |
| rs34145031 | snp | A/G | 0.49703 | 0.0384237 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245972 | CTTGCCAAAGACTTC[A/G]TACAACATCCTTACC | 56916 |
| rs34166467 | in-del | -/A | 0.497933 | 0.032082 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237498 | CTAAAAAAAAAAAAA[-/A]GTAAAAATCACCTGA | 56916 |
| rs34188163 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277861 | GTTTTAAATGGCCTA[C/G]CAGATTTTATGAACC | 56916 |
| rs34207065 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272811 | TTCTTTTTTCTTTCT[C/T]TCCTTTTTCTTTTTA | 56916 |
| rs34216368 | in-del | -/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238947 | TGGATACAACCTCTG[-/C]CCGTCATAAGAGTTT | 56916 |
| rs34231194 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272841 | AAGCAGGTGCTTGCT[C/G]TGTCACCCAGGCTGG | 56916 |
| rs34309015 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254668 | TAAAGACTATATTGT[G/T]TGTTCTAACCATCCA | 56916 |
| rs34315476 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222688 | AAATTGAGGCTGGGC[-/T]TTGGTGGCTCACACC | 56916 |
| rs34320044 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210249 | AGCCTTGATGGCTTC[A/G]GGAAATAAGAAAACT | 56916 |
| rs34355273 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273072 | CAGCGTCCCCAAGTT[C/G]TGGGATTACAGGCAT | 56916 |
| rs34360331 | in-del | -/A | 0.49706 | 0.0382258 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265401 | CTCCTTTTGGGGTAG[-/A]AATACATCAGCAAGG | 56916 |
| rs34364905 | in-del | -/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273163 | GAACATTCTTACCCA[-/C]AGTCCTTTTGCCAAC | 56916 |
| rs34366282 | in-del | -/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287879 | AAGCAGTGGCTGGGC[-/G]GTGTGGTTCATGCTT | 56916 |
| rs34383543 | snp | C/T | 0.49703 | 0.0384237 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242641 | GGGTGCATTAGCTTA[C/T]GCCTATAATCCCAGC | 56916 |
| rs34396188 | snp | A/C | 0.445987 | 0.155207 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270141 | ACATCAGTGAGTAGA[A/C]AGTAGCATGTAAGTG | 56916 |
| rs34417596 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221469 | TCACAATAATCTAAA[A/G]AGGCTATGAAAGTAC | 56916 |
| rs34445238 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272649 | GTTATTGAGATCTAT[C/G]TGTGTTCTTATATGT | 56916 |
| rs34449804 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212650 | CACCACCACAGCCGG[A/C]TAATTTTTGTATTTT | 56916 |
| rs34453443 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238613 | GCAAGACCCTGTCTC[A/G/T]AAAGAAAGAAAGAAA | 56916 |
| rs34491534 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226402 | CTTTTTTTTTTTTTC[-/T]TTTTTTTTTTTTGCC | 56916 |
| rs34519004 | in-del | -/AGTT | 0.49703 | 0.0384237 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280979 | ACAAAAACAATAGAA[-/AGTT]AGTAGACTGTATCTG | 56916 |
| rs34653344 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254818 | TAGCAAGTAAATACA[C/G]ATATGCTTTAAATTT | 56916 |
| rs34655122 | in-del | -/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236445 | ATTAAGAGCCCCTAT[-/C]CCCATTTATCTCGAG | 56916 |
| rs34688220 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272735 | AGTCCGTGGTATAAA[C/T]ACAGTGCAATTTGTT | 56916 |
| rs34728077 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272548 | CCACTATTCTTATAC[A/C]TATCCTCGTGGATTT | 56916 |
| rs34754554 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286858 | GTGTTTAGTTATGAA[A/G]AATCCTGCCCTCTCC | 56916 |
| rs34755772 | in-del | -/TTG | 0.489142 | 0.0728777 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247118 | TGTAGTAATTGCTTA[-/TTG]TTGTTTTGATTGAGA | 56916 |
| rs34760950 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278552 | TTTTTATTTTTATTG[G/T]TTTTAAAACTTAGGT | 56916 |
| rs34769466 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221479 | CTAAAAAGGCTATGA[A/G]AGTACCCCTCCTTTC | 56916 |
| rs34777117 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274529 | ACCATGTTGGCCAGG[C/G]TGGTATCAAACTCCT | 56916 |
| rs34803170 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284611 | TTTTTTTAAGTGGAG[-/A]ACAGGGTTTTGTCAT | 56916 |
| rs34876183 | in-del | -/A | 0.491987 | 0.0627894 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284354 | AAAAAAAAAAAAAAG[-/A]AAAAAAGTAATTTCC | 56916 |
| rs34933276 | in-del | -/CAA | 0.489024 | 0.0732638 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281873 | TAAAAACACCAATAG[-/CAA]CAACAACAACAACAA | 56916 |
| rs34957720 | in-del | -/G | | | frameshift-variant, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208532 | GAGGAGAATGCTGAA[-/G]GGGGAAGTTAGCAGG | 56916 |
| rs34961506 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239056 | GTTAAATGGCAAATT[A/C]CAAGGAAATAAAAAA | 56916 |
| rs34976740 | in-del | -/A | 0.499104 | 0.0211472 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256836 | TGATAAGTTTGTATT[-/A]AAAAAAATCTGCAAG | 56916 |
| rs35038953 | in-del | -/A | 0.375 | 0.216506 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242742 | AAAAAAAAAAAAAAA[-/A]TTTTTTTAATTAGCT | 56916 |
| rs35046977 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272760 | TTTGTTGATCTTCTT[C/G]TGTTGGATATGAATA | 56916 |
| rs35058097 | in-del | -/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249067 | AGTGACAGAGAAGAA[-/G]GGAAAAGTGAGACTA | 56916 |
| rs35059202 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272690 | TTTTTGTTTCTGTTT[G/T]TGTTTTTTTAAATTG | 56916 |
| rs35074327 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235581 | GCTAAATGAAACTTT[-/A]AGTGATATCTTGAGT | 56916 |
| rs35110213 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212618 | CAGCCTCCCAAGTAG[A/C]TGAGACTACAGGTGC | 56916 |
| rs35120457 | in-del | -/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219438 | TTTTGTTTGAAGGAG[-/C]CCTTGATCTTGGACC | 56916 |
| rs35123705 | in-del | -/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235230 | GGCAACCACCAATCC[-/T]TTTTTTTTTTTTTTT | 56916 |
| rs35135866 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272678 | GTATCAGTAATTTTT[G/T]TGTTTCTGTTTTTGT | 56916 |
| rs35175401 | in-del | -/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284722 | GAGGCATGAGCCACT[-/G]GTGCCCAGTCAGTAA | 56916 |
| rs35270685 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275453 | CTTGTGTTACATTAG[G/T]TGATTTATTTAAAGT | 56916 |
| rs35357714 | snp | C/T | 0.027392 | 0.113779 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94278729 | AAAATCTATCAATAA[C/T]TTGGGTATAATCTGA | 56916 |
| rs35361491 | snp | A/G | 0.498059 | 0.0310896 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281341 | TGTATTAAAGAAGCA[A/G]TTTATCACAGAGAAT | 56916 |
| rs35476916 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278126 | GAGAGTTATCTAGGT[A/G]ATCGATACATGACTC | 56916 |
| rs35489656 | snp | A/G | 6.65137e-05 | 0.00576649 | missense, utr-variant-5-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94264710 | TTTATGCTATAGTTC[A/G]CAAAGATGTCCAAAA | 56916 |
| rs35503803 | in-del | -/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279695 | ATCTGGCCCTTTACA[-/G]GGAACAGTTTGCTAA | 56916 |
| rs35540192 | in-del | -/TATCTT | 0.0566069 | 0.158427 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252560 | TTTTTATTTGAAGTC[-/TATCTT]TATATTTATGTATTT | 56916 |
| rs35550209 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272568 | CTCGTGGATTTTTTT[C/G]TGGTTATGTAGTATA | 56916 |
| rs35558307 | snp | G/T | 0.0259695 | 0.110952 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252776 | AAAAAATGTTTTTAA[G/T]CCAAAGAGAGTTGTT | 56916 |
| rs35603756 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264976 | GAATTTATTTCTGTA[-/T]TCGTGCCTAGAAAGT | 56916 |
| rs35617086 | in-del | -/A | | | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94253225 | TTCCTGAAAAAACCC[-/A]AGCTGATTGGCTGGG | 56916 |
| rs35635775 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286943 | AATCTCCGCGCACTG[C/T]AAGCTCCGCCTCCCG | 56916 |
| rs35645033 | in-del | -/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273155 | AAAACTATGAACATT[-/C]CTTACCCAAGTCCTT | 56916 |
| rs35670996 | snp | C/G | 0.499121 | 0.020948 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278328 | AAAATAACTCAGACT[C/G]TAATGAGGGAGATTT | 56916 |
| rs35673086 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254038 | GCCCTGATAAGTGTC[-/T]TTGAAGTGGCAATAG | 56916 |
| rs35681777 | in-del | -/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250844 | CAAGGTAATTATTCT[-/G]GGGTCATAGAAAATA | 56916 |
| rs35699441 | in-del | -/T | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214429 | TAATTTTTTTTTTTT[-/T]GTATTTTTAGTAGAG | 56916 |
| rs35705348 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286909 | TTGCTCTGTCGCCCA[C/G]ACTGGAGTGCAGAGG | 56916 |
| rs35718240 | snp | A/G | 0.450734 | 0.149016 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242879 | CATAATTATGCCACT[A/G]CACTCCAGCCTGGGT | 56916 |
| rs35728606 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223512 | ATAAATAAATAAATA[A/C]CAATAAAGAGAGTTT | 56916 |
| rs35790038 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286921 | CCAGACTGGAGTGCA[C/G]AGGCGCAATCTCCGC | 56916 |
| rs35809016 | in-del | -/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219626 | TCCCTAGGGCCATGG[-/C]AGTCTTCCTGCATAT | 56916 |
| rs35827686 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272610 | CTATACTATTTGTTT[G/T]TGGTTCATTTGGTGC | 56916 |
| rs35833098 | in-del | -/AA | 0.458084 | 0.138567 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238930 | GTTACATGAGGAAAC[-/AA]AGTGGATACAACCTC | 56916 |
| rs35858920 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278601 | GATTATCTTAAACTG[-/T]TTTTTCTGTCTCAGG | 56916 |
| rs35864385 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272527 | GCTTTTTTCCAGTTA[C/G]TGCTACCACTATTCT | 56916 |
| rs35897759 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94283146 | TTGATGAGTTTAATA[-/C]CCGATATGGATATCT | 56916 |
| rs35900615 | in-del | -/G | 0.315516 | 0.241263 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235514 | TGTTATTTTTGACAT[-/G]AATCCACTGGATTTT | 56916 |
| rs35901582 | in-del | -/A | | | frameshift-variant, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252954 | CCTCAGTGTTCTCAG[-/A]AAAAGGCTCAGAAGA | 56916 |
| rs35929831 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273032 | GCTTGTCTCAAACTC[C/G]TGGGCTCAAGTGATC | 56916 |
| rs35940429 | in-del | -/CTTTAT | | | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252563 | TTATTTGAAGTCTAT[-/CTTTAT]ATTTATGTATTTCTA | 56916 |
| rs35940668 | in-del | -/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255013 | TATAATTTGCTTTTT[-/C]CCCTGTTAATCAGTG | 56916 |
| rs35945265 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270562 | AGAAGATCTGAAAAA[C/T]CATTTATGTCTTGGG | 56916 |
| rs35995707 | snp | C/G | 0.49706 | 0.0382258 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245999 | TACCTGCAACAGATT[C/G]TTGGAGAATCATTGC | 56916 |
| rs36000008 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247446 | GAGCAAACAACACAT[A/G]ATAGGCACACCATCT | 56916 |
| rs36026499 | in-del | -/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256721 | AATTGGCCACTTAAA[-/G]GCATGGTAATACATA | 56916 |
| rs36044219 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265249 | CAAATTTGATATCCT[-/A]AAAAAAAGTCAGCTG | 56916 |
| rs36054928 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283679 | AAATACAAAAAATTA[G/T]CCGGGCATGGTGGCG | 56916 |
| rs36080221 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286835 | GCTCTCAAGCCAATA[G/T]CTTTGAAGTGTTTAG | 56916 |
| rs36096369 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259225 | AAGCAACAGAGTTAG[-/T]AAGAATCCTTAATTT | 56916 |
| rs36106229 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272684 | GTAATTTTTTTGTTT[C/G]TGTTTTTGTTTTTTT | 56916 |
| rs41275676 | snp | A/G | 0.0293084 | 0.117453 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208389 | AAGGTGGTGCTTTCT[A/G]CCAATATGAATCTTT | 56916 |
| rs41275677 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264544 | GTGAAACATGTAGCA[A/G]CTCAAATATAAACAT | 56916 |
| rs41275679 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264678 | TCCTAGATCTGAACT[A/G]TTCAATTATTTTTCT | 56916 |
| rs41275681 | snp | A/T | 0.16028 | 0.233346 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270397 | TCAACACAATTCAAT[A/T]TTCTATTATAGATAC | 56916 |
| rs57058059 | in-del | -/GTT | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247123 | TAATTGCTTATTGTT[-/GTT]TTGATTGAGAGGGAC | 56916 |
| rs57104002 | snp | C/G | 0.143959 | 0.226396 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219634 | GGCCATGGAGTCTTC[C/G]TGCATATGCTAATAA | 56916 |
| rs57257091 | in-del | -/GATTTTT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255748 | GAAAATTTGATTTTT[-/GATTTTT]TTTAAAGTATATTAC | 56916 |
| rs57274622 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234813 | GTCTTCGCTGCTACC[A/G]CTACCAGTTCTCCTC | 56916 |
| rs58386866 | snp | A/T | 0.0984431 | 0.198823 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288002 | TTAAAATATATATAT[A/T]TTTTTTTAATTGTTG | 56916 |
| rs58744327 | snp | C/T | 0.135825 | 0.222405 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260511 | ACCACACCCAGTTAA[C/T]TTTTGTATTTTTAGT | 56916 |
| rs58752878 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262936 | TACAGAAAAAAAAAA[-/A]GTGTATTTTGAACTT | 56916 |
| rs59023050 | snp | C/T | 0.135484 | 0.22223 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216369 | ACCTTGTTCATCCTT[C/T]CCTCTAAGTCTTCTG | 56916 |
| rs59106462 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268028 | CCTTTTACATGCTGA[A/G]AAAGGATCTGTAATT | 56916 |
| rs59430254 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222544 | TAATGTATATATTTT[-/T]GAGAGTATATATTAC | 56916 |
| rs60198579 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226528 | TTTTTTTTTTTTTTT[-/T]GATAACAGTGATTTT | 56916 |
| rs60515854 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246365 | ACCTCGTGATCCACC[C/T]GCCTCAGCCTCCCAG | 56916 |
| rs60979294 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265469 | TCTACATATTTCCCC[A/C]ATTTGCTACTTTCAA | 56916 |
| rs61004493 | snp | C/T | 0.49703 | 0.0384237 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242166 | AGCCTCCGGAGTATC[C/T]GGGATTACGGGAGTG | 56916 |
| rs61012480 | snp | A/G | 0.135825 | 0.222405 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244413 | GGAAGTAAATTGAAG[A/G]CAGCTGTGCATGGTG | 56916 |
| rs61050998 | in-del | -/CTAT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285105 | AACTTCAATATTTAT[-/CTAT]ATGACCATGCATCTA | 56916 |
| rs61464369 | in-del | -/GAA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262915 | AAAAAAAGAAAGAAA[-/GAA]AGAAATGGTAGTTGG | 56916 |
| rs61514245 | snp | C/G | 0.49703 | 0.0384237 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243902 | GCCACACAGTACATG[C/G]AGAGGGAATGTTTTG | 56916 |
| rs61519851 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234376 | TGTGAGTTTTTTTGT[A/G]TTTGAATGTTTCTAA | 56916 |
| rs61741696 | snp | A/C | 0.00550178 | 0.0521596 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290736 | GTTTTTATTATACAT[A/C]AGTTTCTTTGTATAA | 56916 |
| rs61741933 | snp | G/T | 0.0259695 | 0.110952 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94273696 | GTCCTCATTTGATCG[G/T]TGTTCCAGCTTCAAC | 56916 |
| rs61750822 | snp | A/G | 0.00977545 | 0.0692255 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252659 | TCCAAATGGAAAAGA[A/G]GTTTCTTCAAGAAGT | 56916 |
| rs61755304 | snp | A/T | 0.000115406 | 0.00759537 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289523 | TTACTAAAAACATCA[A/T]TGGGCCTGTGAAATA | 56916 |
| rs61755305 | snp | A/G | 0.00178755 | 0.0298426 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252612 | TTTTGTCTTTTATAT[A/G]CAGATATGCAATATG | 56916 |
| rs61762661 | snp | A/G | 4.94352e-05 | 0.00497143 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252908 | TCTTCACTTCCTTCA[A/G]GATGCTTCAATTGGT | 56916 |
| rs61762662 | snp | C/G | 0.00404444 | 0.0447869 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94277078 | CAATCTGTTAGAACT[C/G]ATGTCGCTGTTGAAT | 56916 |
| rs62320364 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212726 | TCCTGACTTCAGGCT[A/G]TCTGCCTGCCTTGGC | 56916 |
| rs62320365 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219070 | GCCCACGTTGGCCTC[A/C]CAAAGTGCTGGGATT | 56916 |
| rs62320366 | snp | A/C/T | 0.0138799 | 0.0821421 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221484 | AAGGCTATGAAAGTA[A/C/T]CCCTCCTTTCTCCAA | 56916 |
| rs62320424 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223819 | AACTCCTGACCTTGT[A/G]ATCCGCCCACCTCGG | 56916 |
| rs62320425 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226386 | ATATTTTGGTGACTT[C/T]CCTTTTTTTTTTTTT | 56916 |
| rs62320426 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235639 | TTGTCTGCTAATGTG[A/T]ATTTTTTTTTTTTTT | 56916 |
| rs62320427 | snp | A/G | 0.318656 | 0.240388 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238210 | CCTTTAATTTCCTCC[A/G]GTTTGAGCAAGGAGA | 56916 |
| rs62320428 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238492 | ATTTAAAAAAAAAGT[A/T]AGAGGTGAATGTTAG | 56916 |
| rs62320429 | snp | C/T | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245588 | TTCTGTATCTGGTGT[C/T]AAAAATTTCCATTCA | 56916 |
| rs62320430 | snp | A/G | 0.0691381 | 0.172595 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273589 | TGTTTGTTTTAAAAT[A/G]TTATATATTGTCTTT | 56916 |
| rs62320431 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290307 | TTTCCCTCTCCCGGC[C/T]TTTGCTTCTCTTGAA | 56916 |
| rs66581998 | snp | C/T | 0.497502 | 0.035255 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275750 | ATACCCAAATTGACC[C/T]CCTCCTGGGTATGTA | 56916 |
| rs66791573 | in-del | -/AAACTA | 0.488606 | 0.0746142 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267080 | TAATTTATCAGCCTT[-/AAACTA]AAAAGATTTCTCACA | 56916 |
| rs67474669 | in-del | -/G | 0.16028 | 0.233346 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289097 | AGATTGGTTTTCGTT[-/G]GTTTAGGTTTGGGTT | 56916 |
| rs67552174 | snp | A/G | 0.495056 | 0.049474 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281946 | AGGGAGGCTGAGGTG[A/G]GAGGATTGTTTGAGC | 56916 |
| rs67631469 | in-del | -/TATC | 0.481786 | 0.0936774 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285102 | AGAAACTTCAATATT[-/TATC]TATATGACCATGCAT | 56916 |
| rs67678944 | in-del | -/AGCC | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232837 | AAAAACACAAAAATA[-/AGCC]GGTGTGGTGGCAAGC | 56916 |
| rs68113984 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214266 | TTGAGCGTTCTTTTG[-/T]TTTTTTTTTTTTTTT | 56916 |
| rs70946513 | in-del | -/CCAG | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232838 | AAAACACAAAAATAG[-/CCAG]GTGTGGTGGCAAGCA | 56916 |
| rs70946517 | in-del | -/TAGT | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280982 | AAAACAATAGAAAGT[-/TAGT]AGACTGTATCTGTAT | 56916 |
| rs70946518 | in-del | -/GTTTT/TTT/TTTT | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282103 | TACGTTTTTTTTTTT[-/GTTTT/TTT/TTTT]TTTTTTTTTTTTTTG | 56916 |
| rs70946519 | in-del | -/A | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284177 | TACAAAAAAAAAAAA[-/A]TTAGCCAGGCGTGGT | 56916 |
| rs71581571 | multinucleotide-polymorphism | AA/GC | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245936 | TCTTTAAAACTCTCT[AA/GC]AACGATTTTCCCACT | 56916 |
| rs71581572 | multinucleotide-polymorphism | AA/CT | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247364 | AAGTGTCTGTGTAAC[AA/CT]CCTGGACCACATGAG | 56916 |
| rs71581573 | in-del | -/TTTGATT | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255738 | TTTACATGAGGAAAA[-/TTTGATT]TTTGATTTTTTTTAA | 56916 |
| rs71581574 | in-del | -/TTTATTTTATTTTATTTTA | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275805 | ACATTAACATTTTCT[-/TTTATTTTATTTTATTTTA]TTTTTTTTTTTTTTT | 56916 |
| rs71581575 | in-del | -/TTAG | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280981 | AAAAACAATAGAAAG[-/TTAG]TAGACTGTATCTGTA | 56916 |
| rs71601211 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250104 | TCTTGAAATTTCTTA[C/T]AAGAATTTAAAAAGT | 56916 |
| rs71601212 | snp | G/T | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259951 | TTGTTTTATAGTTTG[G/T]TAGTTTGAATTAAGA | 56916 |
| rs71601213 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277779 | TTTTCTGTGATACTC[A/G]TCCACTGCAAATTAA | 56916 |
| rs71601214 | snp | A/G | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283718 | TAGTCCCAGCTACTA[A/G]GGAGGCTGAGGCAGG | 56916 |
| rs71814441 | in-del | -/TT | 0.462034 | 0.132445 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284577 | TAATTTTGGTTTTTG[-/TT]TTTTTTTTTTTTCGT | 56916 |
| rs72362939 | in-del | -/AAACTA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267081 | AATTTATCAGCCTTA[-/AAACTA]AAAGATTTCTCACAT | 56916 |
| rs72599816 | in-del | -/GTT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247122 | GTAATTGCTTATTGT[-/GTT]TTTGATTGAGAGGGA | 56916 |
| rs72599818 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262914 | AAAAAAAAGAAAGAA[-/A]AAGAAATGGTAGTTG | 56916 |
| rs72665658 | snp | C/T | 0.497091 | 0.0380279 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223610 | TTAAGCTTTTGTTGC[C/T]CAGGCTGGAGTGCAG | 56916 |
| rs72665660 | snp | C/T | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226402 | CCTTTTTTTTTTTTT[C/T]TTTTTTTTTTTTGCC | 56916 |
| rs72665680 | snp | A/G | 0.00748434 | 0.0607137 | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94278750 | TATAATCTGATTTTT[A/G]CTCTTTTATGTGAAA | 56916 |
| rs72665682 | snp | G/T | 0.4941 | 0.0539917 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284577 | TAATTTTGGTTTTTG[G/T]TTTTTTTTTTTTTCG | 56916 |
| rs72886731 | snp | G/T | 0.135484 | 0.22223 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209419 | CTGAGCATAAACTAA[G/T]TAGTTAGTTTCTTAG | 56916 |
| rs72886732 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214090 | TGAGTGGGGACTGAT[C/G]AGTGACCAGTTTCCT | 56916 |
| rs72886740 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259095 | GCCTCCCTTGTGATC[A/G]TTTGACAAAGTTCAT | 56916 |
| rs72886741 | snp | G/T | 0.135825 | 0.222405 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261043 | CAGAAAATATGATAA[G/T]GACAGATTAGATCAC | 56916 |
| rs72886746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276664 | CTAGATGGCCTCTGT[C/T]ACGTATTCTTTGATT | 56916 |
| rs73832564 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225039 | CTCCTAAAATATGTA[A/G]GGGTAAATGGTGGTT | 56916 |
| rs74435082 | snp | C/T | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235228 | CAGGCAACCACCAAT[C/T]CTTTTTTTTTTTTTT | 56916 |
| rs74440606 | snp | A/G | 0.375 | 0.216506 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284353 | AAAAAAAAAAAAAAA[A/G]GAAAAAAGTAATTTC | 56916 |
| rs74464412 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239536 | TTTATTGATGTTGTC[C/T]GGAGTCTCTCTAGCT | 56916 |
| rs74466566 | snp | C/T | 0.159951 | 0.233219 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230532 | TATTGACATTTGGAG[C/T]CAGATAATTCTTTGT | 56916 |
| rs74693226 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236504 | ATTGTCCTTTTTCCC[C/T]TAGAAATTAAAAAAA | 56916 |
| rs74699208 | snp | G/T | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234373 | GGTTGTGAGTTTTTT[G/T]GTGTTTGAATGTTTC | 56916 |
| rs74732339 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224107 | ACTTTGTGTATGATG[A/C]TAATATGTAGGTTTC | 56916 |
| rs74748070 | snp | C/T | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235231 | GCAACCACCAATCCT[C/T]TTTTTTTTTTTTTTT | 56916 |
| rs74750833 | snp | C/T | 0.00901606 | 0.0665338 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249610 | TTAAGACCATTGTTA[C/T]TGATATCTCTTAAAT | 56916 |
| rs74753084 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231444 | GTGGTCAACTCTGTT[A/G]TTCTTACAGGTTTTT | 56916 |
| rs74817205 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211119 | TTCTACTAAAAATAT[A/G]AAATTAGCTGGGCAT | 56916 |
| rs74897961 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271487 | ATGAGTCATGTTCAG[C/G]AAAGAAAATGTTACA | 56916 |
| rs74970312 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273134 | TCCAGTGTTTGGCTA[G/T]TAAGATAAAACTATG | 56916 |
| rs74975674 | snp | C/T | 0.0065578 | 0.0568849 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226078 | AACAGATTCGTTTTC[C/T]AGTTGCTCAAAATAT | 56916 |
| rs74980742 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226864 | TCAGGGAATCGTTTC[C/T]TTTTTTTTTTCTTGT | 56916 |
| rs75021203 | snp | A/G | 0.0387392 | 0.133675 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213197 | GTGTGATAAAACCAT[A/G]TAATAGGGCAAAATA | 56916 |
| rs75089060 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286343 | CCTTCAGTTTTATAC[A/G]TTTGGAGCAAATGGC | 56916 |
| rs75231286 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220918 | GCATCACTGCATACC[A/G]TACAACAGTGATCTC | 56916 |
| rs75413615 | snp | A/G | 0.0425497 | 0.139515 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250876 | ATACTTCTCATTATA[A/G]TCTGTATTTTAGTAT | 56916 |
| rs75419573 | snp | C/T | 0.141258 | 0.225111 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275440 | AGAACTTAATGCTCT[C/T]GTGTTACATTAGTTG | 56916 |
| rs75486436 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285250 | ATTTTTTTGAAGTTT[C/G]TTAAGTTCAAAATTT | 56916 |
| rs75688865 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217927 | TCAGTTACACTTGCA[A/G]ATCTAACAATCTGTG | 56916 |
| rs75734162 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228242 | TATTTTGGAAAAATT[A/G]TAGAAAAGTTGCAAA | 56916 |
| rs75735489 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226401 | CCCTTTTTTTTTTTT[C/T]CTTTTTTTTTTTTGC | 56916 |
| rs75746389 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214868 | TTCAAGGTGGTTGTC[A/G]TATTGAAAGTAGCAC | 56916 |
| rs75823433 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272266 | GGCATTTGAGGTTAC[A/G]ACTCCAACGTATGTA | 56916 |
| rs75832545 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289055 | TCTGAGTCAGTGATT[A/G]TATCTTTAGATGAAA | 56916 |
| rs75841085 | snp | C/T | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283539 | ATGAAGTATTAACAA[C/T]TGACGGCCGGGCGCC | 56916 |
| rs75885551 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264318 | ACTACATTTGATACT[A/G]TTACCTTTGGTATTA | 56916 |
| rs75891233 | in-del | -/T | 0.339656 | 0.233371 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269494 | CTCAGGCAAATTAAG[-/T]TTTTTTTTTTTTTTT | 56916 |
| rs75940197 | snp | A/C | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255405 | GTTGGTGATTATTAA[A/C]TGATTAAATGTAATC | 56916 |
| rs75960165 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254824 | GTAAATACAGATATG[C/T]TTTAAATTTTAATTT | 56916 |
| rs76043758 | snp | C/T | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258712 | TCTTGTCTGTCATTT[C/T]CTAACAGCTTACATA | 56916 |
| rs76085021 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272556 | CTTATACCTATCCTC[A/G]TGGATTTTTTTCTGG | 56916 |
| rs76213764 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219884 | TTTTGCTTTAATATC[C/T]CCCACCTGGTACAAT | 56916 |
| rs76339375 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273315 | TTCACTGTGTCTAAG[C/T]AATAACCAAAATTAT | 56916 |
| rs76377863 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275626 | TTCTTGGATCTAATC[G/T]GCTAGTTTAATAAAA | 56916 |
| rs76550757 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227144 | TGTGGGGGAAAGAGT[A/G]TTCCAGGCATTGGGA | 56916 |
| rs76652041 | snp | C/T | 0.0150606 | 0.0854603 | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291437 | TTACTACTTAGGATG[C/T]ATTCTCATTGGTTCC | 56916 |
| rs76692918 | snp | A/G | 0.375 | 0.216506 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284354 | AAAAAAAAAAAAAAA[A/G]AAAAAAGTAATTTCC | 56916 |
| rs76772324 | snp | C/T | 0.160938 | 0.233598 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223962 | TAGCTTTAGTTCTCA[C/T]TTTTAATACAGTAAA | 56916 |
| rs76778031 | snp | C/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232839 | AAAACACAAAAATAG[C/G]TGTGGTGGCAAGCAC | 56916 |
| rs76834477 | snp | A/G | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247118 | CTGTAGTAATTGCTT[A/G]TTGTTTTGATTGAGA | 56916 |
| rs76855076 | snp | C/G | 0.190519 | 0.242821 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281224 | GGAAGTAATTTAACT[C/G]TTCTTAAAATCAAAA | 56916 |
| rs76926347 | in-del | -/AT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235498 | CATTATTTTTAATCT[-/AT]GTTATTTTTGACATG | 56916 |
| rs76937576 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210088 | AGTATTGGTCATGTG[A/G]AATCTTTAATTTCCT | 56916 |
| rs77038706 | snp | G/T | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275812 | TTTTTTTTTTTTTTT[G/T]TTGAGACGGAGTCTC | 56916 |
| rs77094102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281020 | GTTTTAAAAAAATCT[C/T]AATTGTCATTATTTC | 56916 |
| rs77128337 | snp | C/T | 0.0327778 | 0.123752 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269890 | GTTGCCCAGGCTGGT[C/T]GCGAACTCCTGAGCT | 56916 |
| rs77131730 | snp | C/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235232 | CAACCACCAATCCTT[C/T]TTTTTTTTTTTTTTT | 56916 |
| rs77156280 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216089 | GTATCTCAGGGCCCT[A/G]TTCCTAGACCACAAT | 56916 |
| rs77210576 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279836 | ATCCTTACTGATCTT[C/T]GGTTGAAAGCAACCC | 56916 |
| rs77244286 | snp | A/C | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284331 | GACTCCGTCTCAAAA[A/C]AAAAAAAAAAAAAAA | 56916 |
| rs77271641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268936 | TAACATGTTCCATTT[A/G]TTACTACTTTTATAG | 56916 |
| rs77278686 | snp | C/T | 0.00209497 | 0.032297 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94253274 | TTTGCATAGAAACTT[C/T]GTTCATTTCACTGCA | 56916 |
| rs77484816 | snp | C/T | 0.00454449 | 0.047451 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291058 | TACTACCTCCTTGTA[C/T]ATCACTATACCCAAA | 56916 |
| rs77508247 | snp | A/T | 0.0236746 | 0.106192 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274058 | ACGTAATTAATTCCT[A/T]CACACATAACTGTTC | 56916 |
| rs77562866 | snp | A/T | 0.0494327 | 0.149241 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264477 | ATTTTTTGAGGTAAG[A/T]TATATTTTACTTTAA | 56916 |
| rs77632737 | snp | C/G | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218594 | CTCCTTTATGTTTCA[C/G]CCTTTCTTTTGACTT | 56916 |
| rs77723696 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278230 | ATCATAAAACTTCAA[A/T]ATACATATGGAGCTT | 56916 |
| rs77724320 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260118 | CTAAACTTTTCTGAT[C/T]ATACCTCCCCAGTGT | 56916 |
| rs77753171 | snp | A/G | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284350 | AAAAAAAAAAAAAAA[A/G]AAAGAAAAAAGTAAT | 56916 |
| rs77889526 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232842 | ACACAAAAATAGGTG[G/T]GGTGGCAAGCACCTG | 56916 |
| rs77919033 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277836 | AATTCCCTCCCACTT[A/T]ATGTACAGTGTTTTA | 56916 |
| rs78053376 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249119 | TTAATTAATCTGTTC[A/G]GTTTATACATTATTT | 56916 |
| rs78125891 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232840 | AAACACAAAAATAGG[C/T]GTGGTGGCAAGCACC | 56916 |
| rs78367636 | snp | A/T | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222971 | TCTGTCTCAAAAAAA[A/T]TAAATAAAATAAAAA | 56916 |
| rs78418876 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230360 | TTTTATTTACTTAGC[A/G]TATATGTATATATCT | 56916 |
| rs78480944 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245066 | TTTGTGTTATGTGTG[A/G]CAGAAAATTGCCTTT | 56916 |
| rs78530657 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279457 | GAAAAACACATTTTA[A/G]ACTAAGTTCAAAATG | 56916 |
| rs78569437 | snp | C/T | 0.16028 | 0.233346 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279705 | TTTACAGGAACAGTT[C/T]GCTAACTCCTAGTCT | 56916 |
| rs78811245 | snp | C/T | 0.040671 | 0.13668 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237711 | TTTTAAAAAATCATA[C/T]AATAATTTGTCATGG | 56916 |
| rs78851310 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219852 | AAAAGGGCAAGTTGA[A/G]CTGTAACTTGCCATT | 56916 |
| rs78861010 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258746 | GTAAGCAAATATCTG[C/T]AAGTGGGGTGTAATT | 56916 |
| rs78894912 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249992 | AAAATAACCGTAATA[A/G]AAATTGTGAACTCAT | 56916 |
| rs78931822 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273210 | CATGATTATATTCTT[A/T]AGGGTAGAATTGCTG | 56916 |
| rs78961838 | snp | A/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238049 | TTTTTCGAGGTTTAA[A/T]ATATGTACAAAAATA | 56916 |
| rs79179156 | snp | C/G | 0.47802 | 0.102502 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284309 | TCCAGCCTGGGTGAC[C/G]GAGCAAGACTCCGTC | 56916 |
| rs79225572 | snp | A/G | 0.00637711 | 0.056106 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289581 | AAATATCAACTTGGT[A/G]CACTCAAGGACATTT | 56916 |
| rs79308346 | snp | A/T | | | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94280646 | GAAGATATGGAAGTT[A/T]TGACAGACTTCGAAC | 56916 |
| rs79344163 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259771 | CATCATATTATTTTG[A/G]AGCACATCTCAGACA | 56916 |
| rs79454027 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241137 | ACTAAGGGAATTTAC[A/G]TCTACATTTAATTTG | 56916 |
| rs79462540 | snp | C/G | 0.084364 | 0.187256 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268756 | CTCATCTGTAAAATG[C/G]AGATAATTAATATTT | 56916 |
| rs79515522 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249912 | AAGTATTTTCATACT[A/G]TTTATTTATGTTGTT | 56916 |
| rs79558869 | snp | G/T | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214283 | TTTTTTTTTTTTTTT[G/T]AGACAGTTTCACTCT | 56916 |
| rs79564963 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226640 | TTTATTCTAAAGTCC[A/G]TGAATCAAGTCATTT | 56916 |
| rs79576252 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266848 | AAATACAAATATTCC[A/G]GAATTCCTTGTGAAA | 56916 |
| rs79638874 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271485 | AAATGAGTCATGTTC[A/G]GCAAAGAAAATGTTA | 56916 |
| rs79658182 | snp | C/T | 0.116488 | 0.211364 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286625 | TCTTTCTCCTTTGTC[C/T]AATTCCCTTACACTT | 56916 |
| rs79670517 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272270 | TTTGAGGTTACGACT[C/T]CAACGTATGTATTGT | 56916 |
| rs79865115 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211591 | CAGGACAGAAATTGT[A/G]TGTAGTCAAAATTAC | 56916 |
| rs79865741 | snp | A/G | 0.0005627 | 0.016764 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280797 | TATTAAAAAAGAATG[A/G]CGTTTCTTTTGTATT | 56916 |
| rs79901365 | snp | C/T | 0.00240919 | 0.0346236 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94276474 | CCTTATGACAATTAA[C/T]GTAAGAGAATGTTTG | 56916 |
| rs79932329 | snp | C/G | 0.0345262 | 0.126772 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231795 | TGTTAATCTAGAATG[C/G]GCCACTCCCCTTTTC | 56916 |
| rs80012854 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271488 | TGAGTCATGTTCAGC[A/C]AAGAAAATGTTACAC | 56916 |
| rs80144842 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228481 | CACTAGTACAGTACT[A/G]TTATCTAATATACTT | 56916 |
| rs80160130 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232841 | AACACAAAAATAGGT[A/G]TGGTGGCAAGCACCT | 56916 |
| rs80207279 | snp | A/G | 0.00143251 | 0.0267246 | missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208548 | GGGGAAGTTAGCAGG[A/G]CAAACACTCCTGATT | 56916 |
| rs80286792 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279554 | ACGGCAGTGACTATT[C/T]TTATAAATAAGGTTT | 56916 |
| rs80321042 | snp | G/T | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275813 | TTTTTTTTTTTTTTT[G/T]TGAGACGGAGTCTCA | 56916 |
| rs80323472 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279509 | AGAAGGACTGATAAC[C/T]TACATTATAAGTCAG | 56916 |
| rs111260709 | snp | A/G | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248054 | CATTTTTATGAACAC[A/G]TGTACCCAATGTTTA | 56916 |
| rs111279162 | snp | C/T | 0.481009 | 0.0955756 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282192 | GCAAGCTCCGCCTCC[C/T]GGGTTCACGCCATTC | 56916 |
| rs111356291 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222868 | ACTTGGGAGGCTGAA[A/G]CAGGAGAATCACTTG | 56916 |
| rs111363624 | snp | A/C | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216179 | CTAATCCCATTCATG[A/C]GTGCTCTGCCCCCAT | 56916 |
| rs111376447 | snp | A/T | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258101 | TCCTATATACTTGTC[A/T]TTAGGTCAACTCTAA | 56916 |
| rs111425618 | snp | A/G | | | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94276351 | CAGATATAACTGTGC[A/G]ATCAGCAGTTCTGAT | 56916 |
| rs111438998 | snp | C/G/T | 0.0486741 | 0.148216 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241454 | AGATTAGGTCCCACT[C/G/T]TAATGACCTCATTTT | 56916 |
| rs111497044 | snp | A/G | 0.0256215 | 0.110247 | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291448 | GATGTATTCTCATTG[A/G]TTCCTTCATTGGACT | 56916 |
| rs111497247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270363 | TACTTTTAAGTTCTT[C/T]AATGTGCTAAAAATC | 56916 |
| rs111518265 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232433 | TCAGTCACCTAAGAG[A/G]CAAGGTCAAGTAGGG | 56916 |
| rs111603257 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259127 | CCAATGGGATGTGAG[C/T]AGTGGTATGTTACAA | 56916 |
| rs111604781 | snp | A/C | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273299 | CAGTGGATATTAAAC[A/C]TTCACTGTGTCTAAG | 56916 |
| rs111612865 | snp | A/G | 0.0256215 | 0.110247 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209448 | AGGAAAGGTGAAAGG[A/G]ATGTTGGAAGTTATA | 56916 |
| rs111618601 | snp | C/T | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229474 | CACAAATTTCTCAGT[C/T]TTGGCAGCTGAGGGC | 56916 |
| rs111618858 | snp | G/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239443 | TGTTTTGAAAGTTTG[G/T]TTTTGAATATGAAAT | 56916 |
| rs111672941 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256009 | AAAATTGGAATTTTT[A/G]TTGCCAAATTTCACA | 56916 |
| rs111680557 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257317 | CAAAGATACCCACCA[C/T]TTAAGGTGTTTTGAG | 56916 |
| rs111702430 | in-del | -/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218292 | AATTGTTTTATTTTA[-/T]TTTTTTTTTGAGATA | 56916 |
| rs111707029 | snp | G/T | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265576 | TGTGATCGCCCACAT[G/T]TTGCATGTTGTTGGC | 56916 |
| rs111735355 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284859 | AAGGATATGTTTGTC[A/G]TAATTTTCAAAGTAT | 56916 |
| rs111735714 | snp | C/T | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274668 | GCACTTGTCAAAGTT[C/T]AGTGTTAATTTAACC | 56916 |
| rs111780504 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217417 | ATAGTGTCATATATA[C/T]GATGTATCCTAGATT | 56916 |
| rs111797054 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241174 | TTTTTGCTTTTTAAT[G/T]TATCCAGTATGAAGC | 56916 |
| rs111828975 | in-del | -/ATCT | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285103 | GAAACTTCAATATTT[-/ATCT]ATATGACCATGCATC | 56916 |
| rs111838760 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276179 | ATTAAATACAAGTAC[A/G]TCAGTATTTATTTGA | 56916 |
| rs111900147 | snp | C/T | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283515 | ACATTCCAAATAGTT[C/T]TGCAGTTCATGAAGT | 56916 |
| rs111933287 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244693 | ATGGATGGCTGCCCA[C/T]ATTTGCATTTATATT | 56916 |
| rs111934128 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94290970 | TCACGGCTTAACCCC[A/G]GTCTTGATGGTATAT | 56916 |
| rs112056744 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94290937 | ACAGTGATTATTTAG[A/G]TATTAAAGACTGAGA | 56916 |
| rs112073148 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94290403 | TCTCCATGCATCAGC[A/G]AAATGTTGGTGACAT | 56916 |
| rs112078463 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225376 | TCTCCCTTTTCTTAT[A/G]AGGACATCAGTCATA | 56916 |
| rs112104353 | snp | A/T | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275801 | TTAACATTTTCTTTT[A/T]TTTTTTTTTTTTTGA | 56916 |
| rs112194769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228688 | AACGTAGTTGTTTAC[A/G]TTCTGTTGCTAGTTC | 56916 |
| rs112240665 | snp | A/C | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238929 | AGGTTACATGAGGAA[A/C]CAGTGGATACAACCT | 56916 |
| rs112260483 | snp | C/T | 0.5 | 0 | intron-variant, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208211 | GTTGCGGCCTAACAA[C/T]GAAGCGCAGCCATAA | 56916 |
| rs112303846 | in-del | -/TT | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284956 | ATTTTGTATTTTTTT[-/TT]AGAGAAGTACTAGTT | 56916 |
| rs112325692 | snp | G/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239444 | GTTTTGAAAGTTTGT[G/T]TTTGAATATGAAATT | 56916 |
| rs112326108 | snp | C/T | 0.5 | 0 | missense, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94278953 | CAGAAATGTGCAATG[C/T]CATGATGCAGTTGAG | 56916 |
| rs112344080 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211783 | ACTCTTCCTGCTGAT[A/G]TTTGCATATGACTCA | 56916 |
| rs112344982 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215454 | AGTGAGACCCTGTCT[A/C]TACAAAAAATGAAAA | 56916 |
| rs112371507 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288262 | TCTCTCATTTGTCCC[C/T]TTAATGTCTTTTATA | 56916 |
| rs112402544 | snp | G/T | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265577 | GTGATCGCCCACATT[G/T]TGCATGTTGTTGGCA | 56916 |
| rs112408429 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280539 | TAAACTTTTCTCATC[A/G]TATTATTAATTATTT | 56916 |
| rs112415048 | snp | A/G | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94263675 | AATACTGTGATCACA[A/G]TGATTACTTAGAGTT | 56916 |
| rs112505839 | snp | A/T | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275806 | ATTTTCTTTTTTTTT[A/T]TTTTTTTTGAGACGG | 56916 |
| rs112567098 | snp | A/G | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276622 | TTCTGTAAAAGGGAA[A/G]ATAGTAAATATTTCA | 56916 |
| rs112569297 | snp | A/C | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281888 | CAACAACAACAACAA[A/C]AAAAATAGCCAGGTG | 56916 |
| rs112585242 | snp | C/T | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215016 | TCTTACAGTCTTCTC[C/T]TGGCTTTGCTTAGTT | 56916 |
| rs112594103 | snp | A/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255423 | ATTAAATGTAATCAT[A/T]AGTATTTCATTGTCT | 56916 |
| rs112637945 | snp | C/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283559 | GGCCGGGCGCCGTGG[C/T]TCACGCCTGTAATCC | 56916 |
| rs112723670 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275336 | GAAATTTCATTTTCT[C/G]AATGAAAAATTTGAG | 56916 |
| rs112730246 | snp | C/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94289660 | TTCCATATTACATTT[C/G]TCATAGTATGGACAA | 56916 |
| rs112750518 | snp | A/G | 0.0010961 | 0.0233848 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284926 | AAATAACTATATTTA[A/G]TAACCAATGGACATA | 56916 |
| rs112892417 | snp | G/T | 0.0486741 | 0.148216 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224577 | AGTGCTCAAAAGATT[G/T]CAGATTTTAGAACAT | 56916 |
| rs112907825 | snp | A/G | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262213 | CTGGCTCTTTCTCGA[A/G]AATTTGGTAGCTGCC | 56916 |
| rs112919106 | snp | C/T | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233034 | TTGCTTTTAGATGTT[C/T]TTAGGCATCACATGT | 56916 |
| rs112946431 | snp | C/T | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94270275 | ATTAGGAGTGATTGA[C/T]ACACATTCAGAAAGT | 56916 |
| rs112954423 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289258 | TGGAAAAATAACCTT[A/G]GATTGCTATGTTGGC | 56916 |
| rs112986636 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94251008 | GTTTTTAAATGTTTT[G/T]ACCTGCCTGTTCTTT | 56916 |
| rs113031975 | snp | A/G | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264241 | ATATCTTTTAAGATT[A/G]ATCTTAATATGTAAT | 56916 |
| rs113064362 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279293 | CTGGGACTACAGGCA[C/T]GCACCACCATGCCCG | 56916 |
| rs113075903 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283839 | TCAAAACAAACAAAC[A/C]AAAAAATTGTCTACC | 56916 |
| rs113120915 | in-del | -/T | 0.146314 | 0.227484 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242207 | CCAGCTGTTTTTTTG[-/T]TTTTTTTTTTAATTT | 56916 |
| rs113125319 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269592 | AAAATGATATCTGTG[C/T]CTATGTATAATAGAT | 56916 |
| rs113126273 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231212 | ACAGTGCCCGGAAAC[C/G]CTGGCACATGGAATT | 56916 |
| rs113147234 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219301 | AGGTGTTTTTATTCT[A/G]TTTTGGGAGATCACC | 56916 |
| rs113187276 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234768 | GGAATCATTTAATTG[C/T]AGGTCCTTTGTATTT | 56916 |
| rs113216387 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276769 | TATAAATAATCTTTC[A/G]TCATCTCATAAAGGT | 56916 |
| rs113231382 | snp | A/C | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238930 | GGTTACATGAGGAAA[A/C]AGTGGATACAACCTC | 56916 |
| rs113288196 | snp | A/G | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283004 | AGAAATAACTGCAAT[A/G]CTAAGAGATGTACAT | 56916 |
| rs113356184 | in-del | -/A | 0.00874735 | 0.0655527 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280494 | AAGGTTCTATGATTT[-/A]GATATTTTATCAGGT | 56916 |
| rs113383464 | snp | A/G | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224277 | GTAGGAAATAGAGAA[A/G]TGTTTGTGTTTTGGT | 56916 |
| rs113394539 | snp | A/G | 0.00666511 | 0.0573422 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276514 | CCAAATTACTGTAAA[A/G]TTTAGATTACGTAAT | 56916 |
| rs113395603 | snp | G/T | 0.0256215 | 0.110247 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259675 | CATTGCCTCCCCCAT[G/T]TTGTTATTACAAGAA | 56916 |
| rs113401705 | snp | A/C/G | 0.0256215 | 0.110247 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228267 | TGCAAAAAAAAATGC[A/C/G]TTATCAACTCTCACA | 56916 |
| rs113439733 | snp | A/G | 0.00859407 | 0.064986 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291155 | TATTAATGTATTTTC[A/G]ATGATAGGCTGTTTC | 56916 |
| rs113447166 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289266 | TAACCTTAGATTGCT[A/G]TGTTGGCAATATGAA | 56916 |
| rs113475698 | snp | A/G | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279673 | TTGCCTACAAAGCCT[A/G]AAATATGATCTGGCC | 56916 |
| rs113513413 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219729 | TTTTTATATGGAAGG[A/G]CAGGCTGTTTTCCCT | 56916 |
| rs113541533 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209004 | GGTGCCTAAAGACAA[C/T]CTCTGTACACAAGGG | 56916 |
| rs113543308 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239412 | TATTAAACACTAGGG[A/G]TGTTTTTATGCTGTT | 56916 |
| rs113623653 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252488 | AGTGTATCAAATTTA[A/G]CAATAAATTGTCGTT | 56916 |
| rs113675044 | snp | C/T | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234223 | TCTAAAGATATCTTA[C/T]GTTTGAAGATATTAA | 56916 |
| rs113679218 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273828 | TTTCTTAGTTTGTAG[A/T]GATGAATATTAATTT | 56916 |
| rs113708364 | snp | C/T | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214061 | TAGTAACAAATCCTG[C/T]AGAGAAGTCAAGTTG | 56916 |
| rs113735971 | snp | A/G | 0.190833 | 0.242898 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232782 | AAACTCTGGCAGTAG[A/G]TAAAATCTCCTGGGA | 56916 |
| rs113762549 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287393 | TATTTGTAATTGACT[A/G]TGTATTGCTTTTTGT | 56916 |
| rs113785802 | snp | C/T | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278264 | GAAGTACATGGCAGC[C/T]CAGAATTCAGATGTG | 56916 |
| rs113837033 | snp | A/G | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249846 | CACATAAAAGCTTAG[A/G]GTGAGTTTTGTATTC | 56916 |
| rs113881690 | in-del | -/A | 0 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228635 | GAATATCTTGCAGTG[-/A]AAAAAAAAAAACAGC | 56916 |
| rs113897879 | snp | A/G | 0.5 | 0 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265167 | ACCAGTGTCTTTTTT[A/G]CCTCATAACAGGTAA | 56916 |
| rs113923963 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239763 | GTTTGAGTAGAGATG[A/G]GGTTTCACCATATTG | 56916 |
| rs113979583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271214 | GTGCTTTTTCTACAG[C/T]TGCCTTTAAAATTGT | 56916 |
| rs114029518 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221620 | TAAACCAGAGATTTT[A/G]ACAAATATAAAACAG | 56916 |
| rs114036478 | snp | A/T | 0.0126979 | 0.078662 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207695 | AGGAAATTTTTTTTT[A/T]ATTTTCAACCTTTGT | 56916 |
| rs114079402 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282988 | GTGATATAGCCAGAG[A/G]AGAAATAACTGCAAT | 56916 |
| rs114100389 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271425 | CTTGACCTTTAATCT[A/G]ACATCTCTATTCCTC | 56916 |
| rs114102001 | snp | A/C/G/T | 0.00805044 | 0.0629342 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237047 | AATTTTAAGCCATGT[A/C/G/T]GATTTATTGTTACGT | 56916 |
| rs114109908 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246547 | CAGATAGGTGCGGCC[A/T]TTCTTTTTTCTTAAG | 56916 |
| rs114170690 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224138 | TTCATGTTTATGGCA[A/G]TTAACATGGATGTGA | 56916 |
| rs114203733 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265545 | GGCCAGTACATATTA[A/G]AGTGGTTTTTGTAAT | 56916 |
| rs114217434 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223919 | AGAAAGTAGGACTTT[A/C]TTGTTAAAGTGTTCA | 56916 |
| rs114218124 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94256850 | TTAAAAAAATCTGCA[A/G]GTACATTTTGAGTAC | 56916 |
| rs114242700 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218832 | TAATAACTCTTTTGA[A/G]ACAGAGTCTCACTCT | 56916 |
| rs114243216 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265974 | TTGCTGATCATTGGT[C/T]AATAATTTAAAATCA | 56916 |
| rs114243641 | snp | A/G | 0.030665 | 0.119967 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242325 | GCTGAGATTACAGGC[A/G]TGAGCCACCACGCCC | 56916 |
| rs114252234 | snp | A/G | 0.0013847 | 0.0262761 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94284996 | AATAAGCCAAGGGAC[A/G]ATTGAAGAATCCATG | 56916 |
| rs114343975 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235989 | TCTATTTCAAGTGAT[C/G]CCCTTCAGTTCTAGA | 56916 |
| rs114346958 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271732 | CAGTTGTGTGACTGC[A/G]CTTGGAAATCAGACC | 56916 |
| rs114380615 | snp | A/T | 0.0236746 | 0.106192 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238406 | ATAATGTATACTACT[A/T]CTTATGGTGCCTGGT | 56916 |
| rs114433804 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261650 | CGGGGTCTCACTCTA[C/T]CACCCAGGCTGGAAT | 56916 |
| rs114458559 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249395 | TTTTTTAGGAGATTT[A/T]TCTCATTTTAAGCAC | 56916 |
| rs114517913 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233786 | GCAGATTTTTCACAT[A/G]ACTACACTGAAATGG | 56916 |
| rs114531000 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240346 | CTGTACTCTATGTTA[C/T]ATTCTCTTGTTTTTA | 56916 |
| rs114575489 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229103 | GATGACTCAATTAAC[A/G]TGGCCCCTGCTAGGT | 56916 |
| rs114577983 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279714 | ACAGTTTGCTAACTC[C/G]TAGTCTAGACTTCCA | 56916 |
| rs114580066 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244656 | CAGCCTTTGAGGTTC[A/G]TGTCAGGTATAGCAA | 56916 |
| rs114599607 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266380 | TAAACTATCCTTTCC[A/G]TTAGACTGAGGATTT | 56916 |
| rs114669287 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216095 | CAGGGCCCTATTCCT[A/G]GACCACAATCTTTTA | 56916 |
| rs114678103 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94252366 | CATTTGTGTTCTCAG[A/G]ACCTTTGTTAGAAAA | 56916 |
| rs114703204 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268881 | CTCACCGTTATAGTA[G/T]AAATAATTGTTTTGG | 56916 |
| rs114726255 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276666 | AGATGGCCTCTGTCA[C/T]GTATTCTTTGATTTT | 56916 |
| rs114728539 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216660 | TACCGTTTACGTTGT[C/T]TTTTTATGAATTTGA | 56916 |
| rs114798846 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216419 | ATAAATATACTCATT[C/G]ATATTTTCCTCTAGT | 56916 |
| rs114801247 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284452 | CACTCTGGCTGGAGT[A/G]CAGTGGCACCATCTC | 56916 |
| rs114859467 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245659 | TAAGCTGTAACTCTT[C/G]CAATGTCCACAAGCA | 56916 |
| rs114870347 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260541 | TAGAGACAGGGTTCC[A/G]CTGTGTTGGACTTGA | 56916 |
| rs114879357 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281818 | TTGGGCTCAGGAGTT[C/T]AAGACTACCCTGGAC | 56916 |
| rs114911946 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223136 | ACAGGTGAAAAGATT[A/G]TTCTTCATTTTTTAT | 56916 |
| rs114937311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275589 | CATATGCAGTCTCAA[A/G]CTGCTAGCTATTAAC | 56916 |
| rs114947589 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239286 | ACAGTTTTCAACAAA[A/C]GACCTTTTTAAATAC | 56916 |
| rs114958037 | snp | C/T | 0.00676609 | 0.0577691 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207956 | TGTCGAGGCGCGGGC[C/T]CTGGCAGGTCCTTTC | 56916 |
| rs115007092 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227135 | CCATGTAGATGTGGG[G/T]GAAAGAGTATTCCAG | 56916 |
| rs115026265 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232197 | GACATTATTTATTTT[C/T]TATCACTTGTATTTC | 56916 |
| rs115057865 | snp | C/T | 0.029116 | 0.117091 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242360 | GTATTTTCAGAATAA[C/T]TTATATTCTGAGATG | 56916 |
| rs115105255 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241959 | AAATTTTCTCTGCCA[C/T]GTGTGCACCCTTGGC | 56916 |
| rs115133634 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219130 | TTTTGGTAATCTTCT[A/C]AGAGGGCAAATATAT | 56916 |
| rs115140400 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210473 | AAAAGTCAGTTTAGC[A/G]GTAGTGACTAGTACA | 56916 |
| rs115144771 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258363 | TTTCATGATGTTGGC[C/T]GGGCTGGTCTTGAAC | 56916 |
| rs115161940 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271914 | TTTGTAACCTGTAAA[A/G]CGCAACACAATATTT | 56916 |
| rs115235470 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237791 | CCCTATTAGCACTTA[C/T]GTTTTCATTATTTCA | 56916 |
| rs115302712 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265806 | TGGTATATCCATACT[C/T]TGCAATGTTACACAA | 56916 |
| rs115315663 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224649 | TTACAGATACAGCTC[A/G]TGAGCCCTAATAATG | 56916 |
| rs115449559 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255536 | TTCAAGGTAGTAGAC[A/T]TATAAATGTAATATA | 56916 |
| rs115484243 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225146 | TGTTTTTGAACAGAC[A/G]GATGATACCAATCAT | 56916 |
| rs115492308 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268174 | GTAATAAAACCATTT[C/T]ATGTCCTGATCAAAA | 56916 |
| rs115516781 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94276184 | ATACAAGTACGTCAG[C/T]ATTTATTTGAGTATC | 56916 |
| rs115524539 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215310 | GTAAGTAGGAATCTT[A/G]AGTGCATTTTAAATG | 56916 |
| rs115610633 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218669 | GTATTAGAAACTACT[C/G]TTTAATCTTATATTT | 56916 |
| rs115626685 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269891 | TTGCCCAGGCTGGTC[A/G]CGAACTCCTGAGCTC | 56916 |
| rs115664069 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222972 | CTGTCTCAAAAAAAA[G/T]AAATAAAATAAAAAT | 56916 |
| rs115667532 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94263850 | AGTATTTCAAATAGC[C/T]TTTGGACTTTCTCAT | 56916 |
| rs115701817 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243622 | TAATACATTAGAGAA[C/T]GATTTGAGCATAATC | 56916 |
| rs115735635 | snp | A/G | 0.00465118 | 0.0479995 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264683 | GATCTGAACTATTCA[A/G]TTATTTTTCTTTTTA | 56916 |
| rs115741266 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282896 | ATTAATTGAATCTGA[A/G]TAGTTGAATTGAAGT | 56916 |
| rs115781852 | snp | A/C | 0.0329836 | 0.124112 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235706 | GTATTTTAAAGCAGT[A/C]ATAAGGAAAGAGCTT | 56916 |
| rs115799212 | snp | C/T | 0.000565321 | 0.016803 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264932 | TTGAATATATTTATT[C/T]GTATTTTATCTCAAT | 56916 |
| rs115826782 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215160 | AGGTGTCTGTGGCCA[A/G]AATGTGAGCCATCGT | 56916 |
| rs115872884 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259671 | CCTTCATTGCCTCCC[C/T]CATTTTGTTATTACA | 56916 |
| rs115979990 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229694 | TTTGCTGCTGGTGAG[G/T]TAGGAATTAATGTCA | 56916 |
| rs115980938 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231748 | TTTCAAAACCAAGAT[C/G]TAAATTACATTTGGC | 56916 |
| rs115984326 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279581 | GTTTTACTATAACAC[A/G]GTCATGCCTGTTTTT | 56916 |
| rs116037427 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269029 | ATTGTAAAGACAGAA[C/T]TAGAAAATTATAAAG | 56916 |
| rs116043659 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221080 | TACAAAGAAAACAAC[A/G]CAGTATGTATTTCCA | 56916 |
| rs116048932 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268668 | GATACTGACACTACC[A/T]TTGCAGATACAGATT | 56916 |
| rs116245366 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254138 | CATTAATAATATTCC[A/G]TAGCTTTAAAAAATA | 56916 |
| rs116272196 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212420 | CGTCAAGTGATCCAC[A/G]TGCCTTGGCCTCTGA | 56916 |
| rs116301987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272969 | TGCGCCACCATGCCT[A/G]GCTAATTTTGTATTT | 56916 |
| rs116362138 | snp | A/C | 0.0486741 | 0.148216 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220189 | AGCACTATTCTAATT[A/C]TGATTATTGACTATA | 56916 |
| rs116366742 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245950 | TAAAACGATTTTCCC[A/G]CTGGGGCTTGCCAAA | 56916 |
| rs116381803 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240016 | AAATACTCTGCTTTA[A/C]AATGTTAATAACATT | 56916 |
| rs116400520 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278225 | TACGTATCATAAAAC[C/T]TCAAAATACATATGG | 56916 |
| rs116409616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94209821 | TCACTCTTTGAATAG[A/G]TATTTGACATCCAGG | 56916 |
| rs116428570 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228145 | TCACATGAAGCTGTG[A/G]TAAACATGCCTAATT | 56916 |
| rs116456149 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288813 | CAACTCATCTCAAAA[C/T]ATTCTCAGTGCTAAA | 56916 |
| rs116494299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287682 | GATAAAGCTAAAATC[A/G]GAGAACCACTGCTTT | 56916 |
| rs116521271 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267436 | TGAACTGCTTTAAAC[A/G]AGTCTCTCTAGCCCT | 56916 |
| rs116580633 | snp | A/G | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206456 | TTAAAACAATTGAAC[A/G]TATGAGAAACGGTAG | 56916 |
| rs116616446 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94277739 | ATTCTTGGCTCTCTT[C/G]CACATCACTAATCTT | 56916 |
| rs116681428 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260184 | AAAACGATCATTAGA[A/G]GGTTAAATGCACCCA | 56916 |
| rs116697560 | snp | A/T | 0.000305623 | 0.0123579 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226070 | TAACTAACAACAGAT[A/T]CGTTTTCCAGTTGCT | 56916 |
| rs116705623 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236740 | AGTAAGAATGAGTCA[A/G]CCTGATACATTTTAA | 56916 |
| rs116710489 | snp | A/T | 0.00739429 | 0.0603529 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280545 | TTTCTCATCATATTA[A/T]TAATTATTTTTATTT | 56916 |
| rs116737059 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224674 | ATAATGATTGTTATA[A/G]TTTAGTGTTACGATT | 56916 |
| rs116780735 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249156 | ACTTAAATTCCTTTT[A/G]TCATTGTTTCAGTTT | 56916 |
| rs116802554 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207597 | AAAAAGCCTAGGCTG[C/G]GTGTTGCGTCATCAT | 56916 |
| rs116918311 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261697 | TCACTGCAACCTCTG[A/G]CTCCCGGGCTCAAGC | 56916 |
| rs116920764 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246737 | AGTATAGTGGATCAA[G/T]TGATACTCTCTAGAC | 56916 |
| rs117007065 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269367 | GAGGCATGGCCTTGT[C/T]CTATGTTTTCACATT | 56916 |
| rs117014910 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94209758 | TGAATTTAAATGCTA[C/T]AGGGAACAACTGAAG | 56916 |
| rs117049546 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233237 | ATCTCTATAACTTAC[A/G]TTCATTTGTTACTGT | 56916 |
| rs117159746 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274624 | GCTGGGCCAGTATTT[A/C]CTTTTTATAAAAGAC | 56916 |
| rs117312717 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211706 | CACCACCACATTGTT[C/T]CTTGAATCTTTCAAG | 56916 |
| rs117627865 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231287 | AGAGCTTATGAAGAG[A/C]GAAAAGATTCAGGAG | 56916 |
| rs117651814 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232669 | TTTGAAATACGTACA[C/T]TGGCTAGGCATGGTG | 56916 |
| rs117661863 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241737 | AATGGGAACTCGTTG[G/T]CCTCTGTTCCTTGCA | 56916 |
| rs117844868 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245760 | ATTAGATTGCCTTCT[C/T]TTTTTATATGTCACT | 56916 |
| rs118069856 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278304 | CTAGAATGAATCAAG[A/T]TTCTGCAGAAAATAA | 56916 |
| rs137881650 | snp | A/G | 0.146683 | 0.22877 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284093 | TTGGGAGGCGAAGGC[A/G]GGTGGATCACGAAGT | 56916 |
| rs137906886 | in-del | -/T | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288577 | TTGTTTTGTTTTTTG[-/T]TTTTTTTAACAGAGA | 56916 |
| rs137934376 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209187 | TTAAGATTTCCACTC[G/T]AATCTATGTTCATTG | 56916 |
| rs137953831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259201 | ATGATGGTGGATGTT[A/G]AGGTTATTGAAGCAA | 56916 |
| rs137958578 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242427 | CCAGTTTTTTAAGTC[G/T]TCTTTTTAGCCTCTG | 56916 |
| rs138060877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94236054 | AAGGTTTTAAATCCA[C/T]GTAAAAGAATTCAAG | 56916 |
| rs138072122 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224816 | TTATTTCTCTCTTTC[-/A]TGGGGGATATGTGTC | 56916 |
| rs138160001 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272449 | AGTGACTTTTTACAT[A/T]TATGTACACCCATGT | 56916 |
| rs138212114 | in-del | -/A | | | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94206314 | TTATTTCGCCATTAA[-/A]AAAAAATGAGATCCT | 56916 |
| rs138229956 | snp | C/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287270 | TTGTCTTCAGCTGTG[C/T]CCCGGGTTTCATTTA | 56916 |
| rs138281372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265106 | AGGGTATTTTATTCT[A/G]TCATATCATTATAAA | 56916 |
| rs138316940 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229987 | TTTTAGAATAGCTAC[A/G]CCCATACTACTTGAC | 56916 |
| rs138326521 | snp | C/G/T | 1.65285e-05 | 0.00287471 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94280616 | CATTGTGAGGCTAAC[C/G/T]CTGACCTGATCTTTG | 56916 |
| rs138356016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224487 | TACACCAAGTTTGTG[C/T]GTAAAACAAAGTTTT | 56916 |
| rs138356072 | snp | G/T | 1.64846e-05 | 0.0028709 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94281546 | ATTAAAACATCATCA[G/T]CATAGGTACCTCAGA | 56916 |
| rs138441912 | snp | C/T | 0.000164978 | 0.00908086 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94237008 | TGCCTTGCTGATGTT[C/T]GGTGATGCAGGTATG | 56916 |
| rs138537104 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223216 | TTTAATAAAGAGGGC[C/T]GGGCGTGGTAGCTCA | 56916 |
| rs138549176 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248563 | TCACCAGTATGTCTT[A/C]TTATTCCCCTGCTCA | 56916 |
| rs138553975 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94253208 | TGAATTAAGGGGTGA[G/T]TTTCCTGAAAAAACC | 56916 |
| rs138577616 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219393 | AGTGATTTTTTTTGT[C/T]CGAATGAGCCTTAAT | 56916 |
| rs138620783 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283011 | ACTGCAATACTAAGA[G/T]ATGTACATACATCTT | 56916 |
| rs138680068 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237453 | ATAGAAGCGTGTCCA[C/G]TTTTTAAATAAATGC | 56916 |
| rs138680841 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291715 | GGGGTATGAGGAGAT[G/T]TGGTTTCCATTTGTG | 56916 |
| rs138688809 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231030 | AGCAGTTTAAAAGAC[A/G]TTATTGTCCTTAGTG | 56916 |
| rs138700227 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287921 | ACTTGGGGAGACAGG[C/T]GGGAGGATCGTTTGA | 56916 |
| rs138729457 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223817 | CGAACTCCTGACCTT[A/G]TGATCCGCCCACCTC | 56916 |
| rs138860144 | snp | C/G | 0.000414267 | 0.0143862 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94278634 | CTCAAGCAGTTACCC[C/G]CCAAGAAAGATCGAA | 56916 |
| rs138892699 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235380 | GTTCCTTTTAATGCT[A/G]ACTAATTTAAAGAAA | 56916 |
| rs138927197 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246573 | TTAAGAGTGGAGTTT[C/G]CAACATGCTCCAGAC | 56916 |
| rs138963198 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241969 | TGCCACGTGTGCACC[C/T]TTGGCTGAACATTCA | 56916 |
| rs138973406 | snp | A/G/T | 0.00478085 | 0.0486577 | intron-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94253633 | AATTTCTGGAAGCCT[A/G/T]TAATTCAAGCGTTAG | 56916 |
| rs139034008 | in-del | -/T | 0.160609 | 0.233472 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288262 | CTCTCATTTGTCCCC[-/T]TTAATGTCTTTTATA | 56916 |
| rs139052708 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226904 | AGGTGGGGTCTTGCT[A/G]TGTTGTCCAGGCTGC | 56916 |
| rs139130080 | snp | A/G | 8.25021e-05 | 0.00642217 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94284992 | AACTAATAAGCCAAG[A/G]GACGATTGAAGAATC | 56916 |
| rs139329736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94221372 | GCAAAATGTTTTTTC[A/G]TATGGTTCCAGTTTC | 56916 |
| rs139368008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273809 | TGTCGGAGGGGTGTT[A/G]TGGTTTCTTAGTTTG | 56916 |
| rs139387198 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94266428 | ATAGATGAGAAAAAT[A/T]GTTGTTGTTGTTGTT | 56916 |
| rs139390658 | snp | A/C/G | 0.00755907 | 0.0610114 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238228 | TTGAGCAAGGAGACA[A/C/G]TATTTTGTGGGTGCT | 56916 |
| rs139431297 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255610 | AATATTACCTACTTG[C/G]TAATCTAATTTCAGT | 56916 |
| rs139441785 | in-del | -/A | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225518 | CTTAATTACCTTTTT[-/A]GAGGCCTCATCTCCA | 56916 |
| rs139451649 | snp | A/T | 1.65121e-05 | 0.00287329 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274845 | AAATTAAAAATAAAG[A/T]ACAGCACAATAAATA | 56916 |
| rs139459226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268565 | CTCAGTGTGTTGACC[A/G]TAGGATGGGTGGGTC | 56916 |
| rs139494137 | in-del | -/TTC | 0.0221141 | 0.102801 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244718 | TATATTTTTACTTAG[-/TTC]TTCTCTGTTAAAGAG | 56916 |
| rs139556675 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268123 | CAAACATATATACAC[A/G]TTAATACTTTATATT | 56916 |
| rs139643685 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257679 | ATAGGCTTGTTCTCC[A/G]CCCCCACAAAAAAAA | 56916 |
| rs139681034 | in-del | -/C | 0.0236746 | 0.106192 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271966 | CTAGCATTGCCATAA[-/C]AAAATACCACAGACC | 56916 |
| rs139743463 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289198 | TACCATGAATTAGAT[A/G]CGATCCAGTGTATTA | 56916 |
| rs139782344 | in-del | -/TAAT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274046 | AATTAAACAGATACG[-/TAAT]TAATTCCTACACACA | 56916 |
| rs139817686 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215424 | CCAGGAGTTCAAGAC[A/C]AGCTTGGGCAATGTA | 56916 |
| rs139839410 | snp | C/T | 0.0155632 | 0.0868298 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252777 | AAAAATGTTTTTAAT[C/T]CAAAGAGAGTTGTTG | 56916 |
| rs139857748 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233253 | TTCATTTGTTACTGT[C/T]CTAGTTCTGATCTCT | 56916 |
| rs139869197 | in-del | -/AG | 0.0221141 | 0.102801 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288205 | TCTAAGAAAATAAAC[-/AG]TAATTTTCAGACATT | 56916 |
| rs139893041 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215155 | TTTGTAGGTGTCTGT[C/G]GCCAAAATGTGAGCC | 56916 |
| rs139948330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94225700 | TCTGATTTTATATGC[A/G]TATTAACTTTGTGAT | 56916 |
| rs139950923 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284851 | AAGAATTTAAGGATA[C/T]GTTTGTCGTAATTTT | 56916 |
| rs139993169 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222325 | CACTTTTATTTTCAA[C/G]TATGGTAAGTATCAG | 56916 |
| rs140023690 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212392 | GTTGACCAGGCTAGT[A/G]TCAAACTCCTGACGT | 56916 |
| rs140024964 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261332 | TTGACTGTTATTTAT[C/T]ACTAAACTCATAATA | 56916 |
| rs140065581 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94279885 | ACTTTTTTTTTTGAG[A/G]TAGACTTTTGCTCTT | 56916 |
| rs140147757 | in-del | -/T | 0.0107246 | 0.0724382 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257069 | TTCAGATGCTGACTG[-/T]TTTTTGAAAGAAAAA | 56916 |
| rs140158896 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248793 | TATTTTACTCCATTG[G/T]GCAGAGGAGGTATCA | 56916 |
| rs140204696 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243384 | ACTCAAGTCCATTCT[C/T]AAGTATACCATTTCT | 56916 |
| rs140247144 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94218197 | GTCTATTATTTAGAA[A/G]TCCCTCCTTTAGGTT | 56916 |
| rs140357178 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232392 | AGGAATTATAAAAGG[A/G]TTTTAACCTGAATGC | 56916 |
| rs140417863 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213403 | GAGTCTAATATGTGT[G/T]TGGAGGGTTGGGGGC | 56916 |
| rs140438812 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94229316 | GTTCTAGAACTTAAC[A/T]CTTGTATTTGGTAGT | 56916 |
| rs140447356 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94227586 | AAGGAGTCAAGGATC[A/T]CCCTAAGATTTTTGG | 56916 |
| rs140447675 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284383 | CCATCTGAACACAGA[A/C]CTGTTTGTTGTAATG | 56916 |
| rs140479429 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94244516 | AGAAAACATGTTCTA[G/T]GATTTAAGGCTCCTA | 56916 |
| rs140494651 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94285924 | TGAATGCATAAGGCA[C/G]ATTCTCTTTGGGCAA | 56916 |
| rs140586862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94281296 | CATATATAGGCTGCA[A/G]TAAGACATACGTCTT | 56916 |
| rs140621826 | snp | C/T | 1.64882e-05 | 0.00287121 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94280756 | TCGAGTTTTAGGATG[C/T]ATCTTGTCTGAATTG | 56916 |
| rs140729712 | snp | A/G | 1.65282e-05 | 0.00287469 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94226186 | ATATTTCAAAAATCA[A/G]AGAGGAATACAGTAT | 56916 |
| rs140775182 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257261 | TAAAATTGAAACAGC[A/T]TGTGCAGAAATGAAA | 56916 |
| rs140778263 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216833 | TCCATTCATCCATCA[A/G]TGGGCACTTGGATTG | 56916 |
| rs140779393 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94264438 | ATAGCTGCCAGGGTC[A/G]AAGTAACAAGTTTGG | 56916 |
| rs140863941 | snp | C/T | | | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207228 | ATCCGTCACTAATTA[C/T]CTATACATTTGCAGG | 56916 |
| rs140865682 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250355 | ACATCTACTAAATTC[A/T]GATGAGCTGAATGCA | 56916 |
| rs140868044 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241607 | CAGGTGGATAGGGAA[C/G]GCAAATTCATACTTA | 56916 |
| rs140870431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214253 | GGATTATTGAAAATT[A/G]AGCGTTCTTTTGTTT | 56916 |
| rs140883380 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258503 | AAATCAGGAATCTTA[C/T]CACCTGCTCTGATTT | 56916 |
| rs140967315 | in-del | -/TTT | 0.00398564 | 0.0444627 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250007 | AAAATTGTGAACTCA[-/TTT]ATAACATGTAAGTCA | 56916 |
| rs141008326 | snp | G/T | | | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94207397 | AATATATACTAATTG[G/T]ATTATATATTGTTAT | 56916 |
| rs141036972 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271348 | TTCTCAAATCACATT[G/T]CCTTAAAGCTGAGTT | 56916 |
| rs141149808 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94279171 | TTAAGAAAAACTTTT[C/T]TTTTTCAGACCAGGT | 56916 |
| rs141165740 | snp | C/T | 0.0130921 | 0.0798413 | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291775 | TAAATTTAAGGAATT[C/T]GGATTGTTTTAACTC | 56916 |
| rs141198541 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239007 | GAGCTTTTTCTTATT[C/T]CATTGTACTTCAGAT | 56916 |
| rs141252452 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235883 | AAAATAAGATTGATA[A/T]GCATAATTTCCCTGA | 56916 |
| rs141281758 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235043 | TAAGGCTGGATTTTT[A/T]TTGAGGGTTGGTCAC | 56916 |
| rs141301172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286341 | AACCTTCAGTTTTAT[A/G]CATTTGGAGCAAATG | 56916 |
| rs141319595 | in-del | -/T | 0.0287284 | 0.116357 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94249377 | ATTTGAGGATCATTC[-/T]AGTTTTTTAGGAGAT | 56916 |
| rs141329069 | in-del | -/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219735 | ATGGAAGGACAGGCT[-/G]GTTTTCCCTCCTGTT | 56916 |
| rs141403557 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250661 | AATTCTCTGTTTTCA[A/G]GTGATTAACTTATTT | 56916 |
| rs141441861 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246723 | GTCAACATGATGTCA[G/T]TATAGTGGATCAAGT | 56916 |
| rs141472972 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94220774 | GGTTCTAGTAGTCAA[C/T]GTATTCTTAAAATTG | 56916 |
| rs141625950 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232112 | AGGTAATCCACCCAC[A/G]TCGGCCTCCCAGAGT | 56916 |
| rs141645181 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94253295 | TTTCACTGCAGAAGA[A/G]GAAATTAGAGCTTAC | 56916 |
| rs141669221 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247774 | TTTAGGTGGAATTAT[A/G]TAATATGTAACCTTT | 56916 |
| rs141732145 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223040 | TTTAAGGGAGAAAAA[C/T]AAAGAAAAGGTCAAT | 56916 |
| rs141741301 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273202 | TCATATCTCATGATT[A/G]TATTCTTAAGGGTAG | 56916 |
| rs141863684 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271975 | CCATAACAAAATACC[A/G]CAGACCAAGTGGCTT | 56916 |
| rs141863983 | in-del | -/TAA | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94247698 | ATTCCCTCCTCCCCC[-/TAA]CCCCTGGCAACCGCC | 56916 |
| rs141898407 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267248 | TGTCAGTGATGTGAA[C/T]GCAAATTAACACTGC | 56916 |
| rs141988709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94211530 | GTGGGATAATGCTGC[A/G]TTAGTTTATTTACAG | 56916 |
| rs142082015 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222107 | TGGTACGGAGAGGGT[-/A]CCCCTCCCAGAGGAG | 56916 |
| rs142126477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94269117 | CTATACTTTTAGTTG[C/T]ATTAAATGGGAAATG | 56916 |
| rs142151909 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246374 | TCCACCCGCCTCAGC[C/T]TCCCAGAGTGCTGGG | 56916 |
| rs142173170 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94255349 | TGAATAAAGTACATA[C/T]ATACAATAGTAATTT | 56916 |
| rs142182963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213198 | TGTGATAAAACCATA[C/T]AATAGGGCAAAATAC | 56916 |
| rs142195925 | snp | C/T | 0.000280355 | 0.0118363 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94283286 | AGAAGATAGATGCCA[C/T]AGAGTAGGCCAGACT | 56916 |
| rs142226824 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226489 | AGGTACAATGTGTGT[G/T]TTTTCTGGATAACAG | 56916 |
| rs142230969 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262305 | AGATGGTACCACTAA[C/T]CTGTTAGCATTGAAG | 56916 |
| rs142251241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94280482 | CTGTTACACTAAAAG[A/G]TTCTATGATTTAGAT | 56916 |
| rs142258171 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248980 | TGACTAAAATTTTTC[C/T]TATGCATGAACACAA | 56916 |
| rs142279223 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287126 | GCCTGGCCTCTCCTT[-/A]ACCACTTTTCCTAGA | 56916 |
| rs142282958 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291200 | TTGTTGTTGTTGTTA[C/T]ATCCATACTTTTATC | 56916 |
| rs142288082 | snp | C/G | 0.0150606 | 0.0854603 | upstream-variant-2KB, intron-variant | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94205871 | GGCGTGATCTCGGCT[C/G]ACTGCAAGCTCCGCC | 56916 |
| rs142402491 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237772 | AGGATTAGTTTAACT[A/G]TTTCCCTATTAGCAC | 56916 |
| rs142422899 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288445 | AATTTATGAAGTGTC[A/G]ATTTGGATTTTATGG | 56916 |
| rs142459111 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94209548 | TGTAGCCTGAAAGAT[G/T]GGTAACACACATGTT | 56916 |
| rs142493532 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226864 | TCAGGGAATCGTTTC[-/T]TTTTTTTTTTCTTGT | 56916 |
| rs142551361 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224902 | CCTACGAGAGAATTA[A/T]TGACAGCTATCATTT | 56916 |
| rs142593051 | snp | A/G | 0.000893921 | 0.0211225 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94278704 | ATTTGGGTCTTTTCA[A/G]CAGATTGAAAAAATC | 56916 |
| rs142602472 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228332 | ACAATTGCATTATCA[C/G]TCTTCGTAAACAGCA | 56916 |
| rs142636141 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257695 | CCCCCACAAAAAAAA[A/G]TCTATATCCACCCTT | 56916 |
| rs142642056 | snp | A/C | 0.0663309 | 0.169604 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223295 | GTCAGGAGTTTGAGA[A/C]CAGCCTGGCAGATAT | 56916 |
| rs142678140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94274089 | CATTCTTTCTCAATT[C/T]GTTGGATGTAGAAGT | 56916 |
| rs142693340 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242336 | AGGCGTGAGCCACCA[C/T]GCCCGGCTGTATTTT | 56916 |
| rs142712932 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237475 | AATAAATGCTGACTC[A/G]ATTTTTTTTAACTTA | 56916 |
| rs142858455 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230723 | GAACCCACTGATGTG[C/T]ATGCTAGAAACTCTG | 56916 |
| rs142898417 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284559 | TGTGCCACCACACCC[A/G]GCTAATTTTGGTTTT | 56916 |
| rs142907097 | snp | G/T | 0.462034 | 0.132445 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284579 | ATTTTGGTTTTTGTT[G/T]TTTTTTTTTTTCGTT | 56916 |
| rs142933241 | in-del | -/ATGTATGT | 0.0178098 | 0.0926698 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94240079 | AATTTTTAAGCTGAC[-/ATGTATGT]ATGTATTTGAGCTGC | 56916 |
| rs142934485 | snp | A/G | 0.000307953 | 0.0124049 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94240946 | ATCTTCTTCTTCAGA[A/G]CCATATGAGGAAGAT | 56916 |
| rs142951122 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242158 | CGCACCTCAGCCTCC[A/G]GAGTATCTGGGATTA | 56916 |
| rs142951659 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94248608 | CTTAAAAAAGACTAA[A/C]CTTAGGCTTTATTCC | 56916 |
| rs142992278 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94267007 | AAATCCTTAGTATTT[C/T]TCCTGTTTTATTCTT | 56916 |
| rs143032483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261063 | GATTAGATCACAATA[C/T]GCTAATTTTTTCAGA | 56916 |
| rs143050434 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94253112 | AGCATAGATGGGTGG[C/T]CTTATCCTGTGTAAA | 56916 |
| rs143111719 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286529 | TTTTACTTTATTATC[A/G]AAAATCAGTTTCCAT | 56916 |
| rs143165980 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222386 | GGGACTTAAAGAGTA[C/T]GAAGGGGTTCTGAAT | 56916 |
| rs143203329 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94217128 | TAGCCAACATAATGG[A/G]CATGAGTTTGTATCT | 56916 |
| rs143322691 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214664 | TGAGAACTGAAGAAC[A/C]GTTGGACTGTTTAAC | 56916 |
| rs143364743 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214512 | GACTTGAGATCTGCC[C/T]GCCTCGGCCTCCTAA | 56916 |
| rs143413667 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287352 | CTCTCACAGTGAGGT[C/T]CTTTTCCTCTATAAA | 56916 |
| rs143424650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246930 | GATAACTGCATAGCC[A/G]TATTGATTTGCTCCA | 56916 |
| rs143452525 | snp | C/G/T | 0.013097 | 0.0799021 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94284148 | AACATGGTGAAACCC[C/G/T]GTCTCTACTAAAAAT | 56916 |
| rs143528049 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239685 | TCAAGTGATCCTCAC[A/G]CCTCAGCCTTCCAAG | 56916 |
| rs143537021 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243461 | AAATCAGATACCCAG[A/G]TCACATAACGGCTCA | 56916 |
| rs143631155 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94234667 | ATAAAAATTGACCAA[C/T]TTAGTTTTAGGTAGA | 56916 |
| rs143631261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239107 | AATTAAACTTCCATG[C/T]TGCATCATGGAACGG | 56916 |
| rs143789361 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259324 | TTTAAACCTGTGATA[G/T]TTGGGTTTACTGTCA | 56916 |
| rs143822270 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219433 | GTGATTTTTTGTTTG[A/C]AGGAGCCTTGATCTT | 56916 |
| rs143860571 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94215263 | GGTTAGTGCTGAATT[C/G]TTGTAACAGAAAGTA | 56916 |
| rs143955537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268858 | ATATTCCAGTTTTAG[C/T]ATTTACTCTCACCGT | 56916 |
| rs144010023 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94263361 | CTGATTGTTATCTAT[A/G]CTGCTGCTTATGAAT | 56916 |
| rs144046284 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94261941 | GCAGTTAAAACTTAA[C/T]ACTTCACTTTTTGAA | 56916 |
| rs144128242 | snp | C/T | 3.53594e-05 | 0.00420458 | intron-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94278891 | TCAACAGTTATCCGC[C/T]TGGTTTTATTTTTTA | 56916 |
| rs144157771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216272 | AAGATTTCAACATAC[C/T]GTTTTGGGGAGTGGG | 56916 |
| rs144178841 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94289015 | TGCTGTGCTCAGAAT[A/G]TTGTTTATATGTATA | 56916 |
| rs144231418 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286032 | AATATCCAAATATAT[A/G]GATTTTATTCTAACA | 56916 |
| rs144321938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232506 | TACATCAGGAATGAG[A/G]AGTCTAGGTATAATA | 56916 |
| rs144323304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94287958 | GAGTTCAAAACCAGC[C/T]TGGGCAACATAGCAA | 56916 |
| rs144362581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94250440 | AGCAGTTTGTAAAAG[C/T]CTAGCTGCATATTGA | 56916 |
| rs144402177 | snp | A/G | 9.92146e-05 | 0.00704254 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94264865 | GCTTACTGGAAATGG[A/G]GGTGGATGGAACATA | 56916 |
| rs144409121 | in-del | -/TTT/TTTT | 0.387074 | 0.209071 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94282092 | TTACATGCAAATACG[-/TTT/TTTT]TTTTTTTGTTTTTTT | 56916 |
| rs144426096 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283552 | AATTGACGGCCGGGC[A/G]CCGTGGCTCACGCCT | 56916 |
| rs144526502 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238454 | CAAATGTTAGCAACT[A/G]TTTGTTTAAGGGTCA | 56916 |
| rs144591799 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94231240 | ATTAATTGAATTAAT[A/G]CAGTCTTGAGCACAT | 56916 |
| rs144697057 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94214317 | ACCCAGGCTGGAGTG[C/T]AGTGGCGCAATCTCA | 56916 |
| rs144721996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224306 | GTGCTCTCTAGAGCA[A/G]ATAGTAGTTGTATAG | 56916 |
| rs144737024 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94230928 | TGAGGTGAGGGTGGG[A/G]CCAAATTTTCAAGGA | 56916 |
| rs144737919 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94257365 | TACATTTGTATACTT[C/T]ATACCATGTAAGCAG | 56916 |
| rs144769221 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242453 | CTCTGTTCCTGATAC[A/G]TTGCTGATCTCTACC | 56916 |
| rs144778692 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94275680 | GTTTTAGCTTCACGT[G/T]CTTTTTTGTGCTTAT | 56916 |
| rs145006766 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259627 | CTTAACTGTTAAAGC[A/G]TCCTGAAGTAAGAAT | 56916 |
| rs145067057 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94235151 | AAATAATGCAACTGA[C/T]TCCCAAAAGAAACCT | 56916 |
| rs145122788 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | SMARCAD1 | GRCh38.p7 | 4:94251494 | AATACTGTTGATGGC[A/G]CAGAAAATGATATTC | 56916 |
| rs145125472 | in-del | -/AG | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94254563 | TACTAATTAATCAGC[-/AG]AGTTTAAATTAGTCT | 56916 |
| rs145191107 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213406 | TCTAATATGTGTGTG[A/G]AGGGTTGGGGGCAGA | 56916 |
| rs145269244 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94245863 | TGCAGTAATTTTTGG[A/T]AATATATGTGTCACA | 56916 |
| rs145303992 | snp | A/G | 8.3273e-05 | 0.0064521 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | SMARCAD1 | GRCh38.p7 | 4:94252780 | AATGTTTTTAATCCA[A/G]AGAGAGTTGTTGAAG | 56916 |
| rs145415503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94278129 | AGTTATCTAGGTAAT[C/T]GATACATGACTCATC | 56916 |
| rs145459039 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94212672 | TTGTATTTTTAGTAG[A/G]GACAGGGTTTCACCA | 56916 |
| rs145464259 | snp | A/G | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222654 | TTCTGTTAACTAAGC[A/G]TATTAAAGGTTAATT | 56916 |
| rs145503926 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94228081 | AAAGAGCAAGAGATC[A/G]GACTGTCTACTTCTG | 56916 |
| rs145566308 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94216009 | GGTAGCTTATAAGCA[A/G]TAGAAATCTACTCTT | 56916 |
| rs145651777 | snp | C/G/T | 0.000332623 | 0.0128922 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | SMARCAD1, LOC101929210 | GRCh38.p7 | 4:94208361 | ATAGTTCATTTAAAG[C/G/T]CCCCATCCCTGCAAG | 56916 |
| rs145680198 | snp | A/G | 0.00294608 | 0.038267 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94281489 | TGATAGAGTTGTGTT[A/G]TTTAGCCAATTTACC | 56916 |
| rs145730687 | snp | C/T | 0.0193772 | 0.0965046 | downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291511 | ACAGAGCAAATGAAG[C/T]GAGAGTTGGAGTAAT | 56916 |
| rs145752187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94210192 | TTTTTCCATACATAA[A/G]TTCTGCTTAAAAACT | 56916 |
| rs145778087 | snp | A/G | 0.000206526 | 0.0101597 | | | GRCh38.p7 | 4:94289713 | TCCAAATACTCACAC[A/G]TGAAATTTCAAAAAA | 56916 |
| rs145861633 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94233850 | GCATTTACTATTGAA[A/G]AGAACTGCAGATGTG | 56916 |
| rs145968207 | in-del | -/AAAC | 0.0154538 | 0.0865337 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94283827 | CAAGACTCCATCTCA[-/AAAC]AAACAAACAAAAAAA | 56916 |
| rs146014201 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94224941 | TGAACTAAAGATTCA[A/G]CTGGTCATTGCTTTT | 56916 |
| rs146026094 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94222208 | GTTGTCAACTCATAT[C/T]AATGGTTTGGCATAT | 56916 |
| rs146037318 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94246502 | TTGCCTCCAGTGTGC[A/T]GTGAGCTCCCAATGT | 56916 |
| rs146105981 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241951 | ATCTTTAAAAATTTT[A/C]TCTGCCACGTGTGCA | 56916 |
| rs146148937 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94243104 | TGGGATTACAGGCGT[A/G]TGCCACCATGCTCAG | 56916 |
| rs146244252 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94273796 | GTGTAAGGGTGTGTG[C/T]CGGAGGGGTGTTGTG | 56916 |
| rs146269509 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268465 | TGTATGCCTACCTTA[C/T]CAAGTTTCATTAGTC | 56916 |
| rs146328501 | in-del | -/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226508 | TCTGGATAACAGTGA[-/T]TTTTTTTTTTTTTTT | 56916 |
| rs146391277 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94288710 | AGCCACATCTAATTT[A/G]TAAAATTATTCATAG | 56916 |
| rs146425618 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94213740 | CTTGCTTGGACAGCT[A/G]GAGGATTGACACCAT | 56916 |
| rs146426164 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94268872 | GCATTTACTCTCACC[A/G]TTATAGTAGAAATAA | 56916 |
| rs146452837 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94263961 | TATAGCTTTTACATA[G/T]GAAGTATTCAGTGCC | 56916 |
| rs146471558 | snp | G/T | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94239995 | GGTTAGTGTTTGTAG[G/T]GACACAAATACTCTG | 56916 |
| rs146539278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94238846 | ATCTTATTCAACTTA[C/T]TCATTAATTTCACAA | 56916 |
| rs146576351 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94286107 | ATAAGTCTTTTCTTA[C/T]GGGCTAGTTCATTTC | 56916 |
| rs146669479 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94258630 | TTTTTTTATTCCATT[G/T]GTTTTGTAAGTGCAT | 56916 |
| rs146764169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94262393 | CTACCTCCTGAAGAT[C/T]GTGAATCTTATCAGT | 56916 |
| rs146856538 | snp | A/C | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94271746 | CACTTGGAAATCAGA[A/C]CTGGGTTTGGGGTCC | 56916 |
| rs146884256 | in-del | -/CT | 0.00517822 | 0.0506191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94259377 | ATTCATTCAATTAAA[-/CT]CTTTTTCCTTTAAAA | 56916 |
| rs146898757 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94265698 | CCTTTTTAAAAAAAA[C/T]AATATAAAACTGTTA | 56916 |
| rs146995585 | snp | A/G | 0.000186864 | 0.0096642 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SMARCAD1 | GRCh38.p7 | 4:94291000 | TTGAACAGACTGAAT[A/G]TATTTTACCATTACA | 56916 |
| rs147026624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94272233 | TTCCTCCTGAAAAGC[C/T]TTGTCTCTAAATACA | 56916 |
| rs147098117 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94223214 | TTTTTAATAAAGAGG[G/T]CCGGGCGTGGTAGCT | 56916 |
| rs147108123 | snp | C/T | 4.9489e-05 | 0.00497414 | synonymous-codon, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94276420 | AATTTTTGATGAGGG[C/T]CATATGCTGAAGAAT | 56916 |
| rs147108158 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94219071 | CCCACGTTGGCCTCC[C/T]AAAGTGCTGGGATTA | 56916 |
| rs147140340 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94232114 | GTAATCCACCCACGT[C/T]GGCCTCCCAGAGTGC | 56916 |
| rs147230441 | snp | A/G | 0.000477732 | 0.0154479 | missense, nc-transcript-variant | SMARCAD1 | GRCh38.p7 | 4:94280712 | AACTTTCAGTTAGAC[A/G]TGGACTTGATTTTAG | 56916 |
| rs147236637 | snp | A/T | 0.0236746 | 0.106192 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94260347 | AATACTTTTTATTTT[A/T]TTTTTTTTTATTTTG | 56916 |
| rs147365037 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94242358 | CTGTATTTTCAGAAT[A/C]ACTTATATTCTGAGA | 56916 |
| rs147365475 | in-del | -/TT | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94226527 | TTTTTTTTTTTTTTT[-/TT]GATAACAGTGATTTT | 56916 |
| rs147374814 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94237548 | TACTAAAAAAGTATT[C/T]AAATAGTGAAAGCAA | 56916 |
| rs147383292 | in-del | -/A | | | intron-variant | SMARCAD1 | GRCh38.p7 | 4:94241089 | ATATTATTAGACCTG[-/A]AAATCCACCTAAATG | 56916 |