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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HK1, LOC130003980
(Q18R)
Single nucleotide variant
(missense variant +1 more)
See cases
+1 more
GUncertain significance
HK1
(E847K +6 more)
Single nucleotide variant
(missense variant)
Retinal dystrophy
+3 more
GPathogenic/Likely pathogenic