"PreventionGenetics, part of Exact Sciences"[submitter] AND "GDI1"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 129148	NM_001493.3(GDI1):c.154-3C>T	GDI1	Single nucleotide variant (intron variant)	GDI1-related disorder +3 more	GBenign
Select item 3046325	NM_001493.3(GDI1):c.195G>T (p.Ser65=)	GDI1	Single nucleotide variant (synonymous variant)	GDI1-related disorder	GLikely benign
Select item 3031989	NM_001493.3(GDI1):c.451G>A (p.Asp151Asn)	GDI1 (D151N)	Single nucleotide variant (missense variant)	GDI1-related disorder	GUncertain significance
Select item 587921	NM_001493.3(GDI1):c.570G>A (p.Ala190=)	GDI1	Single nucleotide variant (synonymous variant)	GDI1-related disorder +2 more	GBenign
Select item 2631250	NM_001493.3(GDI1):c.723G>C (p.Leu241Phe)	GDI1 (L241F)	Single nucleotide variant (missense variant)	GDI1-related disorder	GUncertain significance
Select item 3044147	NM_001493.3(GDI1):c.992-10C>T	GDI1	Single nucleotide variant (intron variant)	GDI1-related disorder	GBenign

ClinVar