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Links from OMIM

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KLHL3
(R528H +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic
NR3C2
(S163*)
Single nucleotide variant
(nonsense +1 more)
Autosomal dominant pseudohypoaldosteronism type 1
GPathogenic