List of variants in gene combination CAD, LOC126806171 reported as uncertain significance for disorder of multiple glycosylation

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_004341.5(CAD):c.2525G>A (p.Arg842His)	rs199908899	0.00009
NM_004341.5(CAD):c.2684G>T (p.Gly895Val)	rs759180447	0.00004
NM_004341.5(CAD):c.2492G>A (p.Arg831His)	rs779903352	0.00001
NM_004341.5(CAD):c.2401-5A>G	rs759687469

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