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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SGCD
(T179S +1 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
SGCD
(Q283R +1 more)
Single nucleotide variant
(missense variant)
Autosomal recessive limb-girdle muscular dystrophy type 2F
+6 more
GConflicting classifications of pathogenicity