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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GREB1L
(L665Q +2 more)
Single nucleotide variant
(missense variant)
Scoliosis, isolated, susceptibility to, 1
GUncertain significance
GREB1L
(G1026S +2 more)
Single nucleotide variant
(missense variant)
Scoliosis, isolated, susceptibility to, 1
GUncertain significance