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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYRF
(G108fs +1 more)
Indel
(frameshift variant)
Cardiac-urogenital syndrome
GPathogenic
MYRF
(R695H +1 more)
Single nucleotide variant
(missense variant)
Cardiac-urogenital syndrome
GUncertain significance
MYRF
(R1040G +1 more)
Single nucleotide variant
(missense variant)
Cardiac-urogenital syndrome
GPathogenic
MYRF
(E1041fs +1 more)
Duplication
(frameshift variant)
Cardiac-urogenital syndrome
GPathogenic
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