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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GSAP, LOC101927243
(E27Q)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
GSAP, LOC101927243
(G12R)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance