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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SRGN
(P68R)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
SRGN
(S100F +1 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
SRGN
Single nucleotide variant
(synonymous variant)
not provided
GBenign/Likely benign
ATOH7, CCAR1
+24 more
Deletion
not provided
GPathogenic
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