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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TM9SF4
(Y171H +1 more)
Single nucleotide variant
(missense variant)
TM9SF4-related disorder
GUncertain significance
TM9SF4
(P194A +1 more)
Single nucleotide variant
(missense variant)
TM9SF4-related disorder
GUncertain significance