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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HNRNPDL
(Q110R)
Single nucleotide variant
(missense variant +1 more)
not specified
+1 more
GUncertain significance
HNRNPDL
Deletion
(inframe_deletion +1 more)
Autosomal dominant limb-girdle muscular dystrophy type 1G
GUncertain significance