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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DOCK4-AS1, DOCK4
(F994L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DOCK4, DOCK4-AS1
(A989G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DOCK4, DOCK4-AS1
(I979V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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