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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYRF
(P120S +1 more)
Single nucleotide variant
(missense variant)
Cardiac-urogenital syndrome
+1 more
GUncertain significance
MYRF
(T857A +1 more)
Single nucleotide variant
(missense variant)
Seizure
+2 more
GUncertain significance
MYRF
Single nucleotide variant
(intron variant)
MYRF-related condition
+2 more
GConflicting classifications of pathogenicity
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