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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRSS12
(A606S)
Single nucleotide variant
(missense variant)
Intellectual Disability, Recessive
+1 more
GBenign/Likely benign
PRSS12
Single nucleotide variant
(synonymous variant)
Intellectual disability, autosomal recessive 1
GBenign
PRSS12
(R55T)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign
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