ClinVar Miner

List of variants in gene combination CTSA, LOC130065974 reported as likely benign by Mayo Clinic Laboratories, Mayo Clinic

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_000308.4(CTSA):c.53_54del (p.Leu18fs)	rs562182818	0.01176
NM_000308.4(CTSA):c.54G>C (p.Leu18=)	rs181943893	0.00001

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