Variants in gene ALG6 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 11

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HGVS	dbSNP	gnomAD frequency
NM_013339.4(ALG6):c.391T>C (p.Tyr131His)	rs35383149	0.02935
NM_013339.4(ALG6):c.882T>C (p.Arg294=)	rs145894044	0.00020
NM_013339.4(ALG6):c.1314T>C (p.Ile438=)	rs146939069	0.00006
NM_013339.4(ALG6):c.156G>A (p.Pro52=)	rs751004049	0.00004
NM_013339.4(ALG6):c.167+7T>C	rs374146302	0.00004
NM_013339.4(ALG6):c.618C>T (p.His206=)	rs374336458	0.00004
NM_013339.4(ALG6):c.430-9T>G	rs769256352	0.00001
NM_013339.4(ALG6):c.648C>G (p.Gly216=)	rs1270440540	0.00001
NM_013339.4(ALG6):c.1127+8A>C	rs756307525
NM_013339.4(ALG6):c.450C>A (p.Ile150=)	rs1644492796
NM_013339.4(ALG6):c.495A>G (p.Gln165=)	rs886046471

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