ClinVar Miner

List of intergenic variants studied for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 63
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HGVS dbSNP gnomAD frequency
NC_000007.14:g.67771556T>C rs35629450 0.61823
NC_000007.14:g.67766270A>G rs9691826 0.61804
NC_000007.14:g.67763644A>G rs13307299 0.61708
NC_000007.14:g.67772928A>C rs6964106 0.61672
NC_000007.14:g.67770265T>G rs6946808 0.61055
NC_000017.11:g.41539026C>T rs7212439 0.60455
NC_000007.14:g.67768864T>C rs34912838 0.59939
NC_000011.10:g.56698623C>T rs1397048 0.54056
NC_000011.10:g.56697829T>A rs1509995 0.51757
NC_000011.10:g.56685847C>T rs1588387 0.47558
NC_000011.10:g.56684041A>T rs4340069 0.47502
NC_000011.10:g.121432497G>A rs17125336 0.29501
NC_000011.10:g.121431110C>A rs17125331 0.29484
NC_000017.11:g.19754534C>G rs56191443 0.25779
NC_000011.10:g.121431937A>G rs17125333 0.24576
NC_000011.10:g.121431925T>A rs55736743 0.24553
NC_000011.10:g.121432865T>G rs12417885 0.24366
NC_000011.10:g.121435753G>A rs4146874 0.23813
NC_000005.10:g.4478434A>C rs10066908 0.23511
NC_000006.12:g.135105435A>G rs4895441 0.21408
NC_000023.11:g.103181712T>C rs12854542 0.18235
NC_000018.10:g.22148844T>A rs72879076 0.17859
NC_000007.14:g.67751383T>A rs6977845 0.16536
NC_000017.11:g.7666228C>G rs144366923 0.00672
NC_000020.11:g.30393436C>A rs73621499 0.00285
NC_000016.10:g.177603A>T rs545195355 0.00105
NC_000023.11:g.103181775C>G rs746040794 0.00060
NC_000016.10:g.177596T>G rs930009344 0.00027
GRCh37/hg19 5q15(chr5:92828411-92911270)
NC_000001.11:g.1014545C>T
NC_000001.11:g.151399571C>T
NC_000001.11:g.154628057A>G
NC_000003.12:g.196027293A>G
NC_000007.14:g.67770277A>G rs6942794
NC_000009.12:g.32526235G>C
NC_000011.10:g.56455965_56455966del rs1853510701
NC_000011.10:g.56673649T>C rs7130569
NC_000011.10:g.56685650G>T rs7109249
NC_000011.10:g.56686812G>A rs7113794
NC_000011.10:g.56689664T>C rs55848395
NC_000011.10:g.56693468GTT[6] rs3071452
NC_000012.11:g.9713413A>G rs200950634
NC_000012.12:g.9542835G>T rs2536884
NC_000012.12:g.9542837A>G rs1360001942
NC_000012.12:g.9557442A>G rs79964986
NC_000015.10:g.38565430C>G
NC_000016.10:g.173755A>T rs2261869
NC_000016.10:g.30183126A>C
NC_000017.11:g.41535537G>A rs963478
NC_000018.10:g.22148845C>A rs62092220
NC_000020.11:g.30391112C>T rs4635596
NC_000020.11:g.30393423G>C rs73621498
NC_000020.11:g.30393452C>T rs73621500
NC_000020.11:g.30393488G>A rs62199575
NC_000020.11:g.30399118C>A rs10084493
NM_138348.5(OTULIN):c.-114G>A
Single allele
t(10;14)(p14;q24)dn
t(15;16)(q24;p13)dn
t(1;14)(q25;q11)dn
t(2;14)(p11.2;q11.2)dn
t(6;18)(q14.1;q21.1)dn
t(9;21)(p21;q22)dn

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