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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GOSR2, LOC126862578
+1 more
Single nucleotide variant
(synonymous variant +1 more)
not specified
+4 more
GBenign/Likely benign
GOSR2, LRRC37A2
(G144W +2 more)
Single nucleotide variant
(missense variant +2 more)
not provided
+2 more
GPathogenic
LRRC37A2, GOSR2
(N170S +5 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GUncertain significance
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