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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1632890	NM_031372.4(HNRNPDL):c.969T>G (p.Gly323=)	HNRNPDL	Single nucleotide variant (synonymous variant +1 more)	HNRNPDL-related disorder +1 more	GLikely benign
Select item 1596147	NM_031372.4(HNRNPDL):c.490C>T (p.Leu164=)	HNRNPDL	Single nucleotide variant (synonymous variant +1 more)	Autosomal dominant limb-girdle muscular dystrophy type 1G +1 more	GLikely benign
Select item 705688	NM_031372.4(HNRNPDL):c.282C>T (p.Ser94=)	HNRNPDL	Single nucleotide variant (synonymous variant +1 more)	HNRNPDL-related disorder +1 more	GLikely benign
Select item 464380	NM_031372.4(HNRNPDL):c.114A>G (p.Leu38=)	HNRNPDL	Single nucleotide variant (synonymous variant +1 more)	HNRNPDL-related disorder +1 more	GLikely benign
Select item 464395	NM_031372.4(HNRNPDL):c.98_112del (p.Arg33_Gln37del)	HNRNPDL	Deletion (inframe_deletion +1 more)	Autosomal dominant limb-girdle muscular dystrophy type 1G +1 more	GBenign/Likely benign
Select item 2988639	NM_031372.4(HNRNPDL):c.31C>A (p.Pro11Thr)	HNRNPDL (P11T)	Single nucleotide variant (missense variant +1 more)	Autosomal dominant limb-girdle muscular dystrophy type 1G +1 more	GUncertain significance

ClinVar