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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130003980, HK1
(Q18R)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
HK1
(E847K +6 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GPathogenic/Likely pathogenic