ClinVar Miner

List of variants in gene ALG13 reported as uncertain significance by Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center

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_001099922.3(ALG13):c.2288G>C (p.Gly763Ala)	rs1302894860	0.00003
NM_001099922.3(ALG13):c.834+3A>G	rs370066652	0.00002

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