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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FOXH1
Single nucleotide variant
(synonymous variant)
Holoprosencephaly sequence
+1 more
GBenign
FOXH1
(R137P)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FOXH1
(S113T)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign/Likely benign
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