Variants in gene ALG13 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001099922.3(ALG13):c.2485A>G (p.Met829Val)	rs368075878	0.00046
NM_001099922.3(ALG13):c.2975G>A (p.Cys992Tyr)	rs190790872	0.00027
NM_001099922.3(ALG13):c.3143C>G (p.Ala1048Gly)	rs773401427	0.00023
NM_001099922.3(ALG13):c.2606C>T (p.Ala869Val)	rs138712375	0.00012
NM_001099922.3(ALG13):c.621A>T (p.Gly207=)	rs371428241	0.00008
NM_001099922.3(ALG13):c.2213A>G (p.Glu738Gly)	rs374174400	0.00005
NM_001099922.3(ALG13):c.1005+4A>G	rs758242204	0.00002
NM_001099922.3(ALG13):c.1210G>A (p.Glu404Lys)	rs1272022379	0.00002
NM_001099922.3(ALG13):c.1010T>A (p.Leu337Gln)	rs1189252877	0.00001
NM_001099922.3(ALG13):c.1954G>T (p.Gly652Cys)	rs1164687660	0.00001
NM_001099922.3(ALG13):c.2607G>A (p.Ala869=)	rs746842727	0.00001
NM_001099922.3(ALG13):c.2754ACC[11] (p.Pro942_Pro945del)	rs750710267
NM_001099922.3(ALG13):c.2754ACC[14] (p.Pro945del)	rs750710267
NM_001099922.3(ALG13):c.890G>A (p.Ser297Asn)	rs1939938682

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