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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYP11B1, LOC106799833
(P425S +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CYP11B1, LOC106799833
(E383G)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CYP11B1, LOC106799833
(T319M)
Single nucleotide variant
(missense variant)
Glucocorticoid-remediable aldosteronism
+2 more
GPathogenic/Likely pathogenic
CYP11B1, LOC106799833
(T318M)
Single nucleotide variant
(missense variant)
Deficiency of steroid 11-beta-monooxygenase
+2 more
GPathogenic
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