ClinVar Miner

List of variants in gene MYORG reported as benign for Basal ganglia calcification, idiopathic, 7, autosomal recessive

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_020702.5(MYORG):c.159C>G (p.Asp53Glu)	rs4879781	0.94274
NM_020702.5(MYORG):c.1154T>A (p.Phe385Tyr)	rs7852399	0.22664

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