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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PPM1D
(L45P)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold
GUncertain significance
PPM1D
(H119R)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold
GUncertain significance
PPM1D
(W427fs)
Duplication
(frameshift variant)
Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold
GPathogenic
APPBP2, BCAS3
+12 more
Copy number gain
not provided
GLikely pathogenic
ACE, AMZ2
+77 more
Copy number gain
not provided
GPathogenic
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