List of variants in gene MIB1 reported as uncertain significance for cardiovascular disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_020774.4(MIB1):c.3007A>G (p.Ile1003Val)	rs150652745	0.00099
NM_020774.4(MIB1):c.2746G>A (p.Gly916Arg)	rs147206277	0.00016
NM_020774.4(MIB1):c.2716C>T (p.Arg906Ter)	rs201146927	0.00009
NM_020774.4(MIB1):c.2779+1G>C	rs570099048	0.00001
NM_020774.4(MIB1):c.758A>G (p.Asn253Ser)	rs730880134	0.00001
NM_020774.4(MIB1):c.1207G>T (p.Ala403Ser)	rs1555692389
NM_020774.4(MIB1):c.1322A>G (p.Asn441Ser)	rs730880135
NM_020774.4(MIB1):c.2285A>G (p.Asn762Ser)
NM_020774.4(MIB1):c.2635C>T (p.Gln879Ter)	rs1555696617
NM_020774.4(MIB1):c.2810A>G (p.Asp937Gly)
NM_020774.4(MIB1):c.335G>T (p.Cys112Phe)
NM_020774.4(MIB1):c.442G>A (p.Ala148Thr)	rs369261422
NM_020774.4(MIB1):c.908+5G>A

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.