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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TCIRG1
(R56W)
Single nucleotide variant
(5 prime UTR variant +1 more)
Increased bone mineral density
+3 more
GBenign
TCIRG1
(A417T +2 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
TCIRG1
(V558L +2 more)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign
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