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Links from OMIM

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TAOK1
(R150I)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely pathogenic
PRNP
(M129V)
Single nucleotide variant
(missense variant +1 more)
Inherited prion disease
+7 more
GBenign/Likely benign