List of variants in gene ALG13 reported as uncertain significance for ALG13-related disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001099922.3(ALG13):c.303C>T (p.Asn101=)	rs763113044	0.00003
NM_001099922.3(ALG13):c.1694A>G (p.Tyr565Cys)	rs1159974001	0.00001
NM_001099922.3(ALG13):c.3301G>C (p.Val1101Leu)	rs1370248370	0.00001
NM_001099922.3(ALG13):c.1003A>C (p.Lys335Gln)	rs754059986
NM_001099922.3(ALG13):c.1532A>G (p.Asn511Ser)	rs2525861997
NM_001099922.3(ALG13):c.794G>T (p.Cys265Phe)

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