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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LRRC37A2, WNT3
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign/Likely benign
LRRC37A2, WNT3
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
LRRC37A2, WNT3
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
LRRC37A2, WNT3
(T17S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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