ClinVar Miner

List of variants in gene combination ASIC4, SPEG 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_005876.5(SPEG):c.7742-1327G>A	rs150186936	0.00677
NM_005876.5(SPEG):c.5751G>A (p.Gly1917=)	rs56166111	0.00384

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