ClinVar Miner

List of variants in gene CRTAP reported as benign by Genome Diagnostics Laboratory, The Hospital for Sick Children

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_006371.5(CRTAP):c.641T>C (p.Val214Ala)	rs146124454	0.00061
NM_006371.5(CRTAP):c.558A>G (p.Ala186=)	rs35357409

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