Related gene-specific medical variations for Gene (Select 9987) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2432511	NM_031372.4(HNRNPDL):c.316C>G (p.Arg106Gly)	HNRNPDL (R106G)	Single nucleotide variant (missense variant +1 more)	Autosomal dominant limb-girdle muscular dystrophy type 1G	GUncertain significance
Select item 2432510	NM_031372.4(HNRNPDL):c.266_300del (p.His89fs)	HNRNPDL (H89fs)	Deletion (frameshift variant +1 more)	Autosomal dominant limb-girdle muscular dystrophy type 1G	GUncertain significance
Select item 2432509	NM_031372.4(HNRNPDL):c.101C>G (p.Pro34Arg)	HNRNPDL (P34R)	Single nucleotide variant (missense variant +1 more)	Autosomal dominant limb-girdle muscular dystrophy type 1G	GUncertain significance
Select item 2432508	NM_031372.4(HNRNPDL):c.248C>A (p.Pro83Gln)	HNRNPDL (P83Q)	Single nucleotide variant (missense variant +1 more)	Autosomal dominant limb-girdle muscular dystrophy type 1G	GUncertain significance
Select item 2432507	NM_031372.4(HNRNPDL):c.88T>G (p.Trp30Gly)	HNRNPDL (W30G)	Single nucleotide variant (missense variant +1 more)	Autosomal dominant limb-girdle muscular dystrophy type 1G	GUncertain significance
Select item 2432506	NM_031372.4(HNRNPDL):c.110_113delinsCGCC (p.Gln37_Leu38delinsProPro)	HNRNPDL	Indel (missense variant +1 more)	Autosomal dominant limb-girdle muscular dystrophy type 1G	GUncertain significance
Select item 374519	NM_031372.4(HNRNPDL):c.99_113del (p.Pro34_Leu38del)	HNRNPDL	Deletion (inframe_deletion +1 more)	not provided	GUncertain significance

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