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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PDSS1
(L32M)
Single nucleotide variant
(missense variant +1 more)
Deafness-encephaloneuropathy-obesity-valvulopathy syndrome
GUncertain significance
PDSS1
(I218fs +1 more)
Deletion
(3 prime UTR variant +1 more)
Deafness-encephaloneuropathy-obesity-valvulopathy syndrome
GPathogenic