ClinVar Miner

List of variants in gene MIB1 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 24
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_020774.4(MIB1):c.1829+131T>A rs8098807 0.96525
NM_020774.4(MIB1):c.2050-89del rs3216119 0.83546
NM_020774.4(MIB1):c.2393+10A>G rs11877131 0.09195
NM_020774.4(MIB1):c.1963-89T>C rs2276157 0.09179
NM_020774.4(MIB1):c.*34A>C rs76056004 0.08933
NM_020774.4(MIB1):c.1372-207T>A rs11083356 0.08442
NM_020774.4(MIB1):c.1677+182G>A rs2959512 0.06862
NM_020774.4(MIB1):c.230-203G>C rs1941972 0.03788
NM_020774.4(MIB1):c.1677+90A>T rs2959513 0.03784
NM_020774.4(MIB1):c.703+71T>G rs3017038 0.03780
NM_020774.4(MIB1):c.401+28C>T rs3017048 0.03227
NM_020774.4(MIB1):c.230-29A>C rs3017047 0.03223
NM_020774.4(MIB1):c.1678-210C>T rs45508892 0.03057
NM_020774.4(MIB1):c.2779+299T>C rs73430120 0.01917
NM_020774.4(MIB1):c.1092+172G>A rs114789849 0.01904
NM_020774.4(MIB1):c.1678-138G>A rs28729513 0.01818
NM_020774.4(MIB1):c.1677+70A>G rs9951204 0.01759
NM_020774.4(MIB1):c.2880+335C>T rs9957819 0.01755
NM_020774.4(MIB1):c.1962+17A>G rs139079482 0.00742
NM_020774.4(MIB1):c.1479+18A>G rs12605999 0.00637
NM_020774.4(MIB1):c.908+177GT[12] rs67233506
NM_020774.4(MIB1):c.908+177GT[13] rs67233506
NM_020774.4(MIB1):c.908+177GT[14] rs67233506
NM_020774.4(MIB1):c.908+177GT[17] rs67233506

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.