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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HSD17B3, SLC35D2-HSD17B3
Single nucleotide variant
(intron variant)
not provided
+3 more
GPathogenic
HSD17B3, SLC35D2-HSD17B3
(R80Q)
Single nucleotide variant
(missense variant)
Testosterone 17-beta-dehydrogenase deficiency
+1 more
GPathogenic
HSD17B3, SLC35D2-HSD17B3
(N74T)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic
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