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Items: 16

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RET
(L56M)
Single nucleotide variant
(missense variant)
Hirschsprung disease, susceptibility to, 1
+8 more
GConflicting classifications of pathogenicity
RET
(R67H)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+8 more
GBenign/Likely benign
RET
(T170I +1 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia type 2A
+4 more
GUncertain significance
RET
(V262A +3 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+8 more
GConflicting classifications of pathogenicity
RET
(T278N +3 more)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+8 more
GBenign/Likely benign
RET
(V38M +2 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia type 2B
+9 more
GConflicting classifications of pathogenicity
RET
(V648I +14 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
RET
(G437S +16 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+9 more
GConflicting classifications of pathogenicity
RET
(N763I +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
+1 more
GUncertain significance
RET
(L790F +17 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+5 more
GConflicting classifications of pathogenicity
RET
(Y791F +17 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+9 more
GBenign/Likely benign
RET
(M848K +17 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
RET
(V871I +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
+9 more
GConflicting classifications of pathogenicity
RET
(R982C +17 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+11 more
GConflicting classifications of pathogenicity
RET
(K994N +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
+9 more
GConflicting classifications of pathogenicity
RET
Single nucleotide variant
not provided
GUncertain significance
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