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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FSHR
(G211D +1 more)
Single nucleotide variant
(missense variant)
Ovarian hyperstimulation syndrome
GUncertain significance
FSHR
(G15C)
Single nucleotide variant
(missense variant)
Ovarian dysgenesis 1
GUncertain significance