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Links from MedGen

Items: 1 to 100 of 1334

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WT1
Single nucleotide variant
(non-coding transcript variant +1 more)
Drash syndrome
+3 more
GLikely pathogenic
LOC107982234, WT1
(P136L +1 more)
Single nucleotide variant
(missense variant +1 more)
Drash syndrome
+3 more
GUncertain significance
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Drash syndrome
+3 more
GLikely benign
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Drash syndrome
+3 more
GLikely benign
WT1
Deletion
(nonsense +3 more)
Wilms tumor 1
+3 more
GPathogenic
WT1
(D106G +14 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
Single nucleotide variant
(intron variant)
Wilms tumor 1
+3 more
GLikely benign
LOC107982234, WT1
Duplication
(inframe_insertion +2 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
Single nucleotide variant
(synonymous variant +3 more)
Wilms tumor 1
+3 more
GLikely benign
WT1
(T279fs +3 more)
Deletion
(frameshift variant +1 more)
Wilms tumor 1
+3 more
GPathogenic
LOC107982234, WT1
(S119L +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
Indel
(intron variant)
Wilms tumor 1
+3 more
GUncertain significance
WT1
(F196C +10 more)
Single nucleotide variant
(missense variant +2 more)
Wilms tumor 1
+3 more
GUncertain significance
LOC107982234, WT1
(G186D +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
LOC107982234, WT1
(L85P +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
(L290R +4 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
LOC107982234, WT1
(A66fs)
Deletion
(frameshift variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
(S333R +9 more)
Single nucleotide variant
(missense variant +2 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
Single nucleotide variant
(synonymous variant +1 more)
Wilms tumor 1
+3 more
GLikely benign
WT1
(H111fs +13 more)
Deletion
(frameshift variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
LOC107982234, WT1
(M195V +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Wilms tumor 1
+3 more
GLikely benign
LOC107982234, WT1
(Q26E +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
(T116R +9 more)
Single nucleotide variant
(missense variant +2 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
(S267A +4 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
(N122S +4 more)
Single nucleotide variant
(missense variant +2 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
(V474I +14 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
(D36V +2 more)
Single nucleotide variant
(missense variant +3 more)
Wilms tumor 1
+3 more
GUncertain significance
LOC107982234, WT1
Single nucleotide variant
(intron variant)
Wilms tumor 1
+3 more
GLikely benign
LOC107982234, WT1
(F164S +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
(Y110fs +7 more)
Deletion
(frameshift variant +2 more)
Wilms tumor 1
+3 more
GPathogenic
WT1
Single nucleotide variant
(intron variant)
Wilms tumor 1
+3 more
GLikely benign
WT1
Single nucleotide variant
(intron variant +2 more)
Wilms tumor 1
+3 more
GLikely benign
WT1
Single nucleotide variant
(non-coding transcript variant +1 more)
Wilms tumor 1
+3 more
GLikely benign
LOC107982234, WT1
(F108S +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
LOC107982234, WT1
(D8V +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
(T274I +4 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
LOC107982234, WT1
(N219fs)
Duplication
(frameshift variant +1 more)
Wilms tumor 1
+3 more
GPathogenic
LOC107982234, WT1
Single nucleotide variant
(intron variant)
Wilms tumor 1
+3 more
GLikely benign
WT1
(G105R +8 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
Single nucleotide variant
(intron variant)
Wilms tumor 1
+3 more
GLikely benign
LOC107982234, WT1
(P104S +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
LOC107982234, WT1
(P17S +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
Single nucleotide variant
(intron variant)
Wilms tumor 1
+3 more
GLikely benign
LOC107982234, WT1
(P130L +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
Single nucleotide variant
(synonymous variant +3 more)
Wilms tumor 1
+3 more
GLikely benign
WT1
(V142M +9 more)
Single nucleotide variant
(missense variant +2 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
Single nucleotide variant
(synonymous variant +1 more)
Wilms tumor 1
+3 more
GLikely benign
WT1
(M309R +4 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
(T303I +4 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
(P230Q +4 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
LOC107982234, WT1
(N77K +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
LOC107982234, WT1
(L106P +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Wilms tumor 1
+3 more
GLikely benign
WT1
(S154C +9 more)
Single nucleotide variant
(missense variant +2 more)
Wilms tumor 1
+3 more
GUncertain significance
LOC107982234, WT1
(P33Q +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
LOC107982234, WT1
(A128E +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Wilms tumor 1
+3 more
GLikely benign
WT1
Duplication
(intron variant)
Wilms tumor 1
+3 more
GBenign
LOC107982234, WT1
(G93fs)
Duplication
(frameshift variant +1 more)
Wilms tumor 1
+3 more
GPathogenic
LOC107982234, WT1
(S76fs)
Deletion
(frameshift variant +1 more)
Wilms tumor 1
+3 more
GPathogenic
WT1
(G257C +3 more)
Single nucleotide variant
(missense variant +2 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
(T13K +2 more)
Single nucleotide variant
(missense variant +3 more)
Wilms tumor 1
+3 more
GUncertain significance
LOC107982234, WT1
(G178E +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
Single nucleotide variant
(synonymous variant +2 more)
Wilms tumor 1
+3 more
GLikely benign
WT1
Single nucleotide variant
(intron variant)
Wilms tumor 1
+3 more
GLikely benign
WT1
Single nucleotide variant
(intron variant)
Wilms tumor 1
+3 more
GLikely benign
WT1
Single nucleotide variant
(synonymous variant +1 more)
Wilms tumor 1
+3 more
GLikely benign
WT1
Single nucleotide variant
(intron variant)
Wilms tumor 1
+3 more
GConflicting classifications of pathogenicity
LOC107982234, WT1
(N77D +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
Single nucleotide variant
(synonymous variant +3 more)
Wilms tumor 1
+3 more
GLikely benign
WT1
(Y16C +2 more)
Single nucleotide variant
(missense variant +3 more)
Wilms tumor 1
+3 more
GUncertain significance
LOC107982234, WT1
(F113Y +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
LOC107982234, WT1
(D35A +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
Single nucleotide variant
(synonymous variant +1 more)
Wilms tumor 1
+3 more
GLikely benign
WT1
(G72R +4 more)
Single nucleotide variant
(missense variant +2 more)
Wilms tumor 1
+3 more
GUncertain significance
LOC107982234, WT1
(S150I +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Wilms tumor 1
+3 more
GLikely benign
LOC107982234, WT1
(R19S +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
LOC107982234, WT1
(L43* +1 more)
Single nucleotide variant
(nonsense +1 more)
Wilms tumor 1
+3 more
GUncertain significance
LOC107982234, WT1
(G173R +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
(S359G +10 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
LOC107982234, WT1
(R56* +1 more)
Indel
(nonsense +1 more)
Wilms tumor 1
+3 more
GUncertain significance
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Wilms tumor 1
+3 more
GLikely benign
WT1
Single nucleotide variant
(intron variant)
Wilms tumor 1
+3 more
GLikely benign
LOC107982234, WT1
(C180Y +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
LOC107982234, WT1
(G32E +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
(S364L +9 more)
Single nucleotide variant
(missense variant +2 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
Single nucleotide variant
(intron variant)
Wilms tumor 1
+3 more
GLikely benign
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Wilms tumor 1
+3 more
GLikely benign
WT1
Single nucleotide variant
(intron variant)
Wilms tumor 1
+3 more
GLikely benign
LOC107982234, WT1
(F185V +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
(T206I +11 more)
Single nucleotide variant
(missense variant +2 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
(A335D +9 more)
Single nucleotide variant
(missense variant +2 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
(S324G +4 more)
Single nucleotide variant
(missense variant +2 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
(S281T +4 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
LOC107982234, WT1
(G166R +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Wilms tumor 1
+3 more
GLikely benign
WT1
(S227G +2 more)
Single nucleotide variant
(missense variant +3 more)
Wilms tumor 1
+3 more
GUncertain significance
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Wilms tumor 1
+3 more
GLikely benign
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