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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FRMPD4
(K683E +5 more)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 104
GUncertain significance
FRMPD4
(M1002V +5 more)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 104
GUncertain significance
FRMPD4
(S1197L +5 more)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 104
GLikely benign
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