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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HCCS
(G2D)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
HCCS
(M32T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
HCCS
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign/Likely benign
HCCS
(A174V)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
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