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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FGFR2
(A638G +9 more)
Single nucleotide variant
(missense variant +1 more)
Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis
GUncertain significance
FGFR2
(E601Q +9 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis
GUncertain significance
FGFR2
(C342Y +3 more)
Single nucleotide variant
(missense variant +2 more)
FGFR2-related craniosynostosis
+13 more
GPathogenic/Likely pathogenic
FGFR2
(P253R +3 more)
Single nucleotide variant
(missense variant +2 more)
Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis
+13 more
GPathogenic/Likely pathogenic
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