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Links from MedGen

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129997872, WIPI2
Single nucleotide variant
(splice donor variant)
Intellectual developmental disorder with short stature and variable skeletal anomalies
GUncertain significance
WIPI2
(V184G +3 more)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder with short stature and variable skeletal anomalies
GPathogenic
WIPI2
(R224W +3 more)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder with short stature and variable skeletal anomalies
GUncertain significance
WIPI2
(V249M +3 more)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder with short stature and variable skeletal anomalies
GPathogenic
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