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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
B4GALT7
(S207F)
Single nucleotide variant
(missense variant)
Ehlers-Danlos syndrome progeroid type
+1 more
GUncertain significance
B4GALT7
(R270C)
Single nucleotide variant
(missense variant)
Ehlers-Danlos syndrome, spondylodysplastic type, 1
+3 more
GPathogenic