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Links from MedGen

Items: 1 to 100 of 2781

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RET
(R1005L +17 more)
Single nucleotide variant
(missense variant +1 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(T1022A +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(E335Q +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(G23S)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
Single nucleotide variant
(synonymous variant +1 more)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
(D1030E +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(L1027M +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
Single nucleotide variant
(intron variant)
Multiple endocrine neoplasia, type 2
GLikely benign
LOC106736614, RET
Single nucleotide variant
(5 prime UTR variant)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(G133A +6 more)
Single nucleotide variant
(missense variant +1 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(L1032P +13 more)
Single nucleotide variant
(missense variant +2 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
Single nucleotide variant
(synonymous variant +1 more)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
(A166V +6 more)
Single nucleotide variant
(missense variant +1 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
Single nucleotide variant
(synonymous variant +1 more)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
(P16T +3 more)
Single nucleotide variant
(missense variant +1 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(N351T +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
Single nucleotide variant
(synonymous variant)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
(S153Y)
Single nucleotide variant
(missense variant +1 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(R238G +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(G176A +8 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
RET
(M365R +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
Single nucleotide variant
(5 prime UTR variant +1 more)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
Single nucleotide variant
(synonymous variant +1 more)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
Single nucleotide variant
(synonymous variant +1 more)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
Single nucleotide variant
(synonymous variant)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
Single nucleotide variant
(splice acceptor variant +1 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
Insertion
(intron variant)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
(S155A +6 more)
Single nucleotide variant
(intron variant +1 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(S421L +17 more)
Indel
(missense variant)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
Single nucleotide variant
(synonymous variant)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
(G110A +12 more)
Single nucleotide variant
(intron variant +1 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(N107T +8 more)
Single nucleotide variant
(missense variant +1 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(Q144R +1 more)
Single nucleotide variant
(missense variant +1 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(N219D +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(H303Y +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(R138G +2 more)
Single nucleotide variant
(missense variant +2 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
Duplication
(intron variant)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
(M405I +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(S170T +14 more)
Single nucleotide variant
(missense variant +1 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(P358S +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(P140A)
Single nucleotide variant
(missense variant +1 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(E805K +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(R119C +2 more)
Single nucleotide variant
(intron variant +2 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(P121S +12 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
Single nucleotide variant
(synonymous variant +1 more)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
Single nucleotide variant
(synonymous variant +1 more)
Multiple endocrine neoplasia, type 2
GLikely benign
LOC106736614, RET
(A9S)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(V124M +8 more)
Single nucleotide variant
(missense variant +1 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
Single nucleotide variant
(synonymous variant +1 more)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
(Q117R +6 more)
Single nucleotide variant
(missense variant +1 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
Single nucleotide variant
(intron variant)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
(Q161R +8 more)
Single nucleotide variant
(missense variant +1 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(V196G +3 more)
Single nucleotide variant
(missense variant +1 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
Single nucleotide variant
(intron variant)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
Single nucleotide variant
(intron variant +1 more)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
Single nucleotide variant
(intron variant)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
(E1006G +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(V174L +8 more)
Single nucleotide variant
(intron variant +1 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(S216P +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
Single nucleotide variant
(intron variant)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
(D102H)
Single nucleotide variant
(missense variant +1 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
Single nucleotide variant
(synonymous variant)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
Single nucleotide variant
(intron variant)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
(R499S +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
Duplication
(inframe_insertion +1 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(I142M +12 more)
Single nucleotide variant
(intron variant +1 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(C100F +8 more)
Single nucleotide variant
(missense variant +1 more)
Multiple endocrine neoplasia, type 2
+1 more
GUncertain significance
RET
Single nucleotide variant
(intron variant)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
Single nucleotide variant
(synonymous variant +2 more)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
(A26V)
Single nucleotide variant
(missense variant +1 more)
Multiple endocrine neoplasia, type 2
+1 more
GUncertain significance
RET
(Y1062S +17 more)
Single nucleotide variant
(missense variant +1 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(R114L)
Single nucleotide variant
(missense variant +1 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(D224G +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(K264N +12 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(Y505S +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
Single nucleotide variant
(intron variant)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
Single nucleotide variant
(intron variant)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
Single nucleotide variant
(intron variant)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
Single nucleotide variant
(intron variant)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
(T39A +6 more)
Single nucleotide variant
(missense variant +1 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(Q187E +1 more)
Single nucleotide variant
(intron variant +1 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
Single nucleotide variant
(synonymous variant +1 more)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
Single nucleotide variant
(synonymous variant +2 more)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
(I574F +17 more)
Single nucleotide variant
(missense variant +1 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
Deletion
(intron variant)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
Single nucleotide variant
(synonymous variant)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
(E467G +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
Single nucleotide variant
(intron variant)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
(A281T +3 more)
Single nucleotide variant
(missense variant +1 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
Single nucleotide variant
(intron variant)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
(S1071C +13 more)
Single nucleotide variant
(missense variant +2 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
RET
Single nucleotide variant
(synonymous variant)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
Single nucleotide variant
(intron variant)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
Single nucleotide variant
(intron variant)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
Single nucleotide variant
(intron variant)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
(C120Y +2 more)
Single nucleotide variant
(missense variant +2 more)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
(Y178F +12 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
Single nucleotide variant
(intron variant +1 more)
Multiple endocrine neoplasia, type 2
GLikely benign
RET
(K302N +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
GUncertain significance
RET
Single nucleotide variant
(intron variant)
Multiple endocrine neoplasia, type 2
GLikely benign
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