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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IGSF1
(N1214K +2 more)
Single nucleotide variant
(missense variant)
X-linked central congenital hypothyroidism with late-onset testicular enlargement
GUncertain significance
IGSF1
(G1012R +2 more)
Single nucleotide variant
(missense variant)
X-linked central congenital hypothyroidism with late-onset testicular enlargement
GUncertain significance