ClinVar Miner

List of variants in gene MED25 reported as benign by CeGaT Center for Human Genetics Tuebingen

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.1727C>G (p.Ala576Gly)	rs193291405	0.00836
NM_030973.4(MED25):c.93C>T (p.Tyr31=)	rs61742955	0.00394

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