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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DHCR7, NADSYN1
(V126I)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+3 more
GUncertain significance
NADSYN1, DHCR7
Single nucleotide variant
(intron variant)
Inborn genetic diseases
+3 more
GBenign/Likely benign