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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KIF7, LOC126862216
(S1122W)
Single nucleotide variant
(missense variant)
Acrocallosal syndrome
GUncertain significance
KIF7
(V828M)
Single nucleotide variant
(missense variant)
Acrocallosal syndrome
+3 more
GUncertain significance