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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYP11B1, LOC110673972
(R30Q)
Single nucleotide variant
(missense variant)
not provided
+2 more
GLikely benign
CYP11B1, LOC110673972
(C10Y)
Single nucleotide variant
(missense variant)
Glucocorticoid-remediable aldosteronism
+2 more
GLikely benign
CYP11B1, LOC110673972
(V9A)
Single nucleotide variant
(missense variant)
not specified
+2 more
GUncertain significance
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