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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130001123, LRATD2
(E202Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC130001123, LRATD2
(V181M)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC130001123, LRATD2
(L170V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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