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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FREM2
Single nucleotide variant
(synonymous variant)
not specified
+4 more
GBenign
FREM2
(F1070S)
Single nucleotide variant
(missense variant)
Fraser syndrome 1
+4 more
GBenign/Likely benign
FREM2
Single nucleotide variant
(intron variant)
not provided
+2 more
GBenign
FREM2
(T2326I)
Single nucleotide variant
(missense variant)
not provided
+4 more
GBenign
FREM2
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GBenign
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