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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC106029312, NCF1
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign/Likely benign
LOC106029312, NCF1
(N166D)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign/Likely benign
LOC106029312, NCF1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
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