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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ZSWIM6
(H228R)
Single nucleotide variant
(missense variant)
Acromelic frontonasal dysostosis
GUncertain significance
ZSWIM6
(M664T)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ZSWIM6
(R761W)
Single nucleotide variant
(missense variant)
Acromelic frontonasal dysostosis
+1 more
GUncertain significance
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