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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SOHLH1
(K236fs)
Deletion
(frameshift variant)
Nonsyndromic hypergonadotropic hypogonadism
GLikely pathogenic
SOHLH1
(Y9*)
Single nucleotide variant
(nonsense)
Nonsyndromic hypergonadotropic hypogonadism
+1 more
GPathogenic/Likely pathogenic