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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYRIP
(R67Q)
Single nucleotide variant
(synonymous variant +2 more)
not provided
GBenign
MYRIP
Single nucleotide variant
(intron variant)
not provided
GBenign
EIF1B-AS1, MYRIP
(P137L +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign/Likely benign
EIF1B-AS1, MYRIP
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
EIF1B-AS1, MYRIP
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign/Likely benign
ACAA1, ACVR2B
+93 more
Deletion
not provided
GPathogenic
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