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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC108281177, SOX2
+1 more
Microsatellite
(inframe_insertion)
Anophthalmia/microphthalmia-esophageal atresia syndrome
GUncertain significance
LOC108281177, SOX2
+1 more
(L82fs)
Deletion
(frameshift variant)
Anophthalmia/microphthalmia-esophageal atresia syndrome
GPathogenic
LOC108281177, SOX2
+1 more
(Y160*)
Single nucleotide variant
(nonsense)
Anophthalmia/microphthalmia-esophageal atresia syndrome
+1 more
GPathogenic
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