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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130061627, USH1G
(K438I +1 more)
Indel
(missense variant)
not provided
GUncertain significance
LOC130061627, USH1G
(K335fs +1 more)
Deletion
(frameshift variant)
not provided
GPathogenic/Likely pathogenic