ClinVar Miner

List of variants in gene combination CRTAP, LOC129936436 reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 1

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HGVS	dbSNP	gnomAD frequency
NM_006371.5(CRTAP):c.18G>C (p.Arg6=)	rs1333081449

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