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Links from MedGen

Items: 1 to 100 of 307

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RET
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
+5 more
GLikely benign
RET
Single nucleotide variant
(synonymous variant)
Multiple endocrine neoplasia, type 2a
+5 more
GLikely benign
RET
Single nucleotide variant
(intron variant)
Multiple endocrine neoplasia, type 2a
+5 more
GLikely benign
RET
Single nucleotide variant
(intron variant)
Pheochromocytoma
+5 more
GLikely benign
RET
Single nucleotide variant
(intron variant)
Hirschsprung disease, susceptibility to, 1
+5 more
GLikely benign
RET
Single nucleotide variant
(synonymous variant +1 more)
Familial medullary thyroid carcinoma
+6 more
GLikely benign
RET
Single nucleotide variant
(intron variant)
Pheochromocytoma
+5 more
GLikely benign
RET
Single nucleotide variant
(intron variant)
Familial medullary thyroid carcinoma
+5 more
GLikely benign
RET
Single nucleotide variant
(intron variant)
Familial medullary thyroid carcinoma
+5 more
GLikely benign
RET
Single nucleotide variant
(intron variant)
Pheochromocytoma
+5 more
GLikely benign
RET
Single nucleotide variant
(intron variant)
Familial medullary thyroid carcinoma
+5 more
GLikely benign
RET
Single nucleotide variant
(synonymous variant +1 more)
Familial medullary thyroid carcinoma
+7 more
GLikely benign
RET
(L827P +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2b
+5 more
GUncertain significance
RET
(P198S +1 more)
Single nucleotide variant
(missense variant)
Familial medullary thyroid carcinoma
+5 more
GUncertain significance
RET
(E1058D +17 more)
Single nucleotide variant
(missense variant)
Hirschsprung disease, susceptibility to, 1
+5 more
GUncertain significance
RET
(N610S +12 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2b
+6 more
GUncertain significance
RET
(K806R +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2b
+6 more
GUncertain significance
RET
Single nucleotide variant
(intron variant)
Multiple endocrine neoplasia, type 2
+7 more
GConflicting classifications of pathogenicity
RET
Single nucleotide variant
(synonymous variant)
Multiple endocrine neoplasia, type 2
+5 more
GLikely benign
RET
Single nucleotide variant
(synonymous variant +1 more)
Familial medullary thyroid carcinoma
+7 more
GBenign/Likely benign
RET
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+6 more
GLikely benign
RET
Single nucleotide variant
(synonymous variant)
Multiple endocrine neoplasia, type 2
+5 more
GLikely benign
RET
Single nucleotide variant
(synonymous variant)
Multiple endocrine neoplasia, type 2
+6 more
GLikely benign
RET
(R189C +1 more)
Single nucleotide variant
(missense variant)
Hirschsprung disease, susceptibility to, 1
+6 more
GUncertain significance
RET
(F150del)
Microsatellite
(inframe_indel +1 more)
Multiple endocrine neoplasia, type 2b
+6 more
GUncertain significance
RET
(N356H +12 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
RET
(D1042N +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2b
+5 more
GUncertain significance
RET
(N151I)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+6 more
GUncertain significance
RET
Deletion
(inframe_indel)
Multiple endocrine neoplasia, type 2b
GLikely pathogenic
RET
(V1075fs)
Duplication
(frameshift variant)
Multiple endocrine neoplasia, type 2a
+2 more
GConflicting classifications of pathogenicity
RET
(K757E +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
+6 more
GUncertain significance
RET
(Y761C +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
+7 more
GUncertain significance
RET
(R226P +2 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+6 more
GUncertain significance
RET
(R693H +17 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+7 more
GUncertain significance
RET
(S462L +8 more)
Single nucleotide variant
(missense variant)
Ovarian cancer
+7 more
GConflicting classifications of pathogenicity
RET
(P20Q)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+7 more
GUncertain significance
RET
(P1047L +17 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+6 more
GUncertain significance
RET
(F600S +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2b
+2 more
GUncertain significance
RET
Single nucleotide variant
(synonymous variant +2 more)
Hereditary cancer-predisposing syndrome
+6 more
GConflicting classifications of pathogenicity
RET
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+6 more
GConflicting classifications of pathogenicity
RET
(R624fs +1 more)
Deletion
(frameshift variant)
Multiple endocrine neoplasia, type 2b
GPathogenic
RET
(V388F +6 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2b
GUncertain significance
RET
(D517E +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2b
GUncertain significance
RET
(P60S)
Single nucleotide variant
(missense variant)
Hirschsprung disease, susceptibility to, 1
+6 more
GUncertain significance
RET
(A350V +12 more)
Single nucleotide variant
(missense variant)
Hirschsprung disease, susceptibility to, 1
+6 more
GUncertain significance
RET
(S148F)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+6 more
GUncertain significance
RET
(M1064I)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+7 more
GConflicting classifications of pathogenicity
RET
Single nucleotide variant
(intron variant)
Multiple endocrine neoplasia, type 2
+5 more
GUncertain significance
RET
(Y1062H +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
+6 more
GUncertain significance
RET
(R43H +3 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2b
+6 more
GUncertain significance
RET
(R563H +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2b
+6 more
GUncertain significance
RET
(E762D +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2b
+6 more
GUncertain significance
RET
(V201I +8 more)
Single nucleotide variant
(missense variant)
Hirschsprung disease, susceptibility to, 1
+6 more
GUncertain significance
RET
Single nucleotide variant
(synonymous variant +1 more)
Multiple endocrine neoplasia, type 2b
+5 more
GLikely benign
RET
Single nucleotide variant
(synonymous variant +2 more)
Multiple endocrine neoplasia, type 2
+6 more
GLikely benign
RET
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+6 more
GLikely benign
RET
Single nucleotide variant
(intron variant)
Pheochromocytoma
+5 more
GLikely benign
RET
Single nucleotide variant
(synonymous variant +1 more)
Pheochromocytoma
+6 more
GLikely benign
RET
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+6 more
GLikely benign
RET
Single nucleotide variant
(intron variant +1 more)
Hereditary cancer-predisposing syndrome
+7 more
GLikely benign
RET
(S650A +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
+6 more
GUncertain significance
RET
(R234Q +2 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+7 more
GConflicting classifications of pathogenicity
RET
(K535E +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2b
+6 more
GConflicting classifications of pathogenicity
RET
(K483Q +17 more)
Single nucleotide variant
(missense variant)
Hirschsprung disease, susceptibility to, 1
+8 more
GUncertain significance
RET
(G28S)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
+7 more
GConflicting classifications of pathogenicity
RET
(V804M +35 more)
Single nucleotide variant
(missense variant)
Medullary thyroid carcinoma
GPathogenic
RET
(P218S +2 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+6 more
GUncertain significance
RET
(R721Q +17 more)
Single nucleotide variant
(missense variant)
Hirschsprung disease, susceptibility to, 1
+7 more
GUncertain significance
RET
(A919P +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
+7 more
GUncertain significance
RET
(K710R +17 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+8 more
GUncertain significance
RET
(V145I)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2b
+8 more
GConflicting classifications of pathogenicity
RET
(R475W +8 more)
Single nucleotide variant
(missense variant)
not provided
+7 more
GUncertain significance
RET
(K728E +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
+6 more
GUncertain significance
RET
(P516R +12 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
+7 more
GUncertain significance
RET
(R133H)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+7 more
GConflicting classifications of pathogenicity
RET
(S201T +1 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
+7 more
GUncertain significance
RET
(N1059S +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
+6 more
GUncertain significance
RET
(S339L +3 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+6 more
GConflicting classifications of pathogenicity
RET
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+6 more
GLikely benign
RET
Single nucleotide variant
(synonymous variant +1 more)
Multiple endocrine neoplasia, type 2a
+6 more
GLikely benign
RET
Single nucleotide variant
(synonymous variant)
Multiple endocrine neoplasia, type 2b
+6 more
GLikely benign
RET
Single nucleotide variant
(synonymous variant)
Pheochromocytoma
+7 more
GLikely benign
RET
(P1067S)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+7 more
GConflicting classifications of pathogenicity
RET
(G849D +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2a
+5 more
GUncertain significance
RET
(S645del +14 more)
Deletion
(inframe_indel +1 more)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
RET
(G385V +6 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2b
+6 more
GUncertain significance
RET
(R886Q +17 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+8 more
GConflicting classifications of pathogenicity
RET
(P117H)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2a
+6 more
GUncertain significance
RET
(A999V +17 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+6 more
GUncertain significance
RET
(D380N +6 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2a
+5 more
GUncertain significance
RET
(V193L +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+6 more
GUncertain significance
RET
Single nucleotide variant
(intron variant)
Hirschsprung disease, susceptibility to, 1
+7 more
GConflicting classifications of pathogenicity
RET
(M1008L +17 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+6 more
GUncertain significance
RET
Single nucleotide variant
(synonymous variant)
Multiple endocrine neoplasia, type 2b
+6 more
GLikely benign
RET
(N151S)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
+7 more
GConflicting classifications of pathogenicity
RET
(E673A +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
+8 more
GUncertain significance
RET
(A764T +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2b
+6 more
GConflicting classifications of pathogenicity
RET
(H246N +2 more)
Single nucleotide variant
(missense variant)
Hirschsprung disease, susceptibility to, 1
+6 more
GConflicting classifications of pathogenicity
RET
(R368C +6 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
+7 more
GConflicting classifications of pathogenicity
LOC106736614, RET
(G7D)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
+7 more
GUncertain significance
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