"GeneDx"[submitter] AND "LOC105376032"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1280907	NM_016734.3(PAX5):c.604+206G>A	LOC105376032, PAX5	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1221158	NM_016734.3(PAX5):c.604+98C>A	LOC105376032, PAX5	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1268399	NM_016734.3(PAX5):c.476-33T>C	LOC105376032, PAX5	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1242955	NM_016734.3(PAX5):c.476-302T>C	LOC105376032, PAX5	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1254532	NM_016734.3(PAX5):c.475+253_475+254dup	LOC105376032, PAX5	Duplication (intron variant)	not provided	GLikely benign
Select item 1242616	NM_016734.3(PAX5):c.475+253dup	LOC105376032, PAX5	Duplication (intron variant)	not provided	GBenign
Select item 1254756	NM_016734.3(PAX5):c.475+15T>A	LOC105376032, PAX5	Single nucleotide variant (intron variant)	not provided	GBenign/Likely benign
Select item 135000	NM_016734.3(PAX5):c.451G>A (p.Val151Ile)	LOC105376032, PAX5 (V151I +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign/Likely benign

ClinVar