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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYP21A2, LOC106780800
Single nucleotide variant
(5 prime UTR variant +1 more)
Inborn genetic diseases
+4 more
GPathogenic/Likely pathogenic
CYP21A2, LOC106780800
(P454S +2 more)
Single nucleotide variant
(missense variant)
CYP21A2-related condition
+4 more
GPathogenic/Likely pathogenic