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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHRNG
(R46Q)
Single nucleotide variant
(missense variant)
Autosomal recessive multiple pterygium syndrome
GUncertain significance
CHRNG
(S133fs)
Deletion
(frameshift variant)
not provided
+2 more
GPathogenic
CHRNG
(P134fs)
Deletion
(frameshift variant)
Autosomal recessive multiple pterygium syndrome
+3 more
GPathogenic
CHRNG
(V154fs)
Duplication
(frameshift variant)
Autosomal recessive multiple pterygium syndrome
+4 more
GPathogenic
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