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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126862088, TRPM1
(E1191fs +2 more)
Deletion
(frameshift variant)
not provided
+1 more
GPathogenic/Likely pathogenic
LOC126862088, TRPM1
(Q1161H +2 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GLikely benign