List of variants in gene MED25 reported as benign by GeneDx

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: 21

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_030973.4(MED25):c.180+238T>C	rs1674134	0.65229
NM_030973.4(MED25):c.180+227A>G	rs1674133	0.60275
NM_030973.4(MED25):c.180+108G>C	rs1674132	0.54824
NM_030973.4(MED25):c.1482+200A>G	rs1290652	0.54801
NM_030973.4(MED25):c.306-27del	rs5828413	0.53718
NC_000019.10:g.49818255C>G	rs968388	0.27374
NM_030973.4(MED25):c.1375-55T>C	rs3745480	0.27008
NC_000019.10:g.49818253C>T	rs7246170	0.15330
NM_030973.4(MED25):c.1230+148C>T	rs1530882	0.05823
NM_030973.4(MED25):c.165G>A (p.Thr55=)	rs77400039	0.01828
NM_030973.4(MED25):c.1483-7C>T	rs2017698	0.01612
NM_030973.4(MED25):c.-12A>G	rs114843375	0.01532
NM_030973.4(MED25):c.2031G>A (p.Ala677=)	rs57854058	0.01517
NM_030973.4(MED25):c.1482+19G>A	rs4802632	0.00704
NM_030973.4(MED25):c.819+14C>T	rs188257265	0.00166
NM_030973.4(MED25):c.354C>T (p.Leu118=)	rs145574885	0.00110
NM_030973.4(MED25):c.135-6T>G	rs199743509	0.00036
NM_030973.4(MED25):c.1230+177C>T	rs4801809
NM_030973.4(MED25):c.1674+19C>T	rs752522
NM_030973.4(MED25):c.234C>G (p.Pro78=)	rs74863643
NM_030973.4(MED25):c.597C>A (p.Ala199=)	rs149788020

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.