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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HSD17B10
(R217Q +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic
HSD17B10
(V65A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
HSD17B10
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
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