ClinVar Miner

List of variants in gene MED25 reported as likely benign by Genetic Services Laboratory, University of Chicago

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_030973.4(MED25):c.275A>T (p.Tyr92Phe)	rs549136898	0.00023
NM_030973.4(MED25):c.1572C>T (p.Gly524=)	rs559482732	0.00005

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