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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126806608, WNT7A
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
LOC126806608, WNT7A
Single nucleotide variant
(synonymous variant)
WNT7A-related disorder
GLikely benign
LOC126806608, WNT7A
Single nucleotide variant
(synonymous variant)
WNT7A-related disorder
GLikely benign
LOC126806608, WNT7A
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign/Likely benign
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