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Links from MedGen

Items: 1 to 100 of 2468

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC107982234, WT1
(R24fs)
Deletion
(frameshift variant +1 more)
Wilms tumor 1
GUncertain significance
LOC107982234, WT1
(G26fs)
Deletion
(frameshift variant +1 more)
Wilms tumor 1
GUncertain significance
WT1
(V112I +11 more)
Single nucleotide variant
(missense variant +2 more)
Wilms tumor 1
GUncertain significance
LOC107982234, WT1
(P129Q +2 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
GUncertain significance
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Wilms tumor 1
GLikely benign
WT1
Single nucleotide variant
(synonymous variant +2 more)
Wilms tumor 1
GLikely benign
WT1
Single nucleotide variant
(3 prime UTR variant +1 more)
Wilms tumor 1
GUncertain significance
WT1
(Q11H +5 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
GUncertain significance
WT1
Single nucleotide variant
(intron variant)
Wilms tumor 1
GLikely benign
LOC107982234, WT1
(K141Q +2 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
GUncertain significance
LOC107982234, WT1
(Q142P +2 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
GUncertain significance
WT1
(V14A +5 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
GUncertain significance
WT1
Single nucleotide variant
(intron variant)
Wilms tumor 1
GLikely benign
WT1
Single nucleotide variant
(synonymous variant +3 more)
Wilms tumor 1
GLikely benign
WT1
Single nucleotide variant
(intron variant)
Wilms tumor 1
GLikely benign
WT1
Single nucleotide variant
(synonymous variant +2 more)
Wilms tumor 1
GLikely benign
LOC107982234, WT1
(R56G +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
GUncertain significance
LOC107982234, WT1
(F3V)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
GUncertain significance
WT1
Single nucleotide variant
(synonymous variant +1 more)
Wilms tumor 1
GLikely benign
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Wilms tumor 1
GLikely benign
LOC107982234, WT1
(T17K +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
GUncertain significance
LOC107982234, WT1
(A125S +2 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
GUncertain significance
WT1
Single nucleotide variant
(synonymous variant +2 more)
Wilms tumor 1
GLikely benign
WT1
(R195G +12 more)
Single nucleotide variant
(missense variant +2 more)
Wilms tumor 1
GUncertain significance
WT1
Single nucleotide variant
(3 prime UTR variant +1 more)
Wilms tumor 1
GUncertain significance
LOC107982234, WT1
(R59L +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
GUncertain significance
LOC107982234, WT1
(P22S +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
GUncertain significance
LOC107982234, WT1
(A46D +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
GUncertain significance
LOC107982234, WT1
(P4A +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
GUncertain significance
WT1
(N173S +3 more)
Single nucleotide variant
(missense variant +3 more)
Wilms tumor 1
GUncertain significance
LOC107982234, WT1
(P133T +2 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
GUncertain significance
WT1
(P205S +5 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
GUncertain significance
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Wilms tumor 1
GLikely benign
WT1
Single nucleotide variant
(synonymous variant +1 more)
Wilms tumor 1
GLikely benign
WT1
(V114M +5 more)
Single nucleotide variant
(missense variant +2 more)
Wilms tumor 1
GUncertain significance
WT1
(T151K +3 more)
Single nucleotide variant
(missense variant +3 more)
Wilms tumor 1
GUncertain significance
LOC107982234, WT1
(V105L +2 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
GUncertain significance
LOC107982234, WT1
(G19D +2 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
GUncertain significance
LOC107982234, WT1
(A149T +2 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
GUncertain significance
WT1
(H108Q +11 more)
Single nucleotide variant
(missense variant +2 more)
Wilms tumor 1
GUncertain significance
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Wilms tumor 1
GLikely benign
LOC107982234, WT1
(D75G +2 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
GUncertain significance
WT1
Deletion
(intron variant)
Wilms tumor 1
GUncertain significance
LOC107982234, WT1
(P12T +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
GUncertain significance
WT1
(M241T +5 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
GUncertain significance
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Wilms tumor 1
GLikely benign
LOC107982234, WT1
(M1V +2 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
GUncertain significance
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Wilms tumor 1
GLikely benign
LOC107982234, WT1
(P16R +2 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
GUncertain significance
WT1
Single nucleotide variant
(synonymous variant +3 more)
Wilms tumor 1
GLikely benign
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Wilms tumor 1
GLikely benign
WT1
(Y110F +11 more)
Single nucleotide variant
(missense variant +2 more)
Wilms tumor 1
GUncertain significance
LOC107982234, WT1
(G44S +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
GUncertain significance
LOC107982234, WT1
Insertion
(inframe_insertion +2 more)
Wilms tumor 1
GUncertain significance
WT1
(Y12H +5 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
GUncertain significance
GPC3
(R86L)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
GUncertain significance
GPC3
(V525M +3 more)
Single nucleotide variant
(missense variant)
Wilms tumor 1
GUncertain significance
GPC3
Single nucleotide variant
(synonymous variant)
Wilms tumor 1
GBenign
GPC3
(A112T +2 more)
Single nucleotide variant
(missense variant)
Wilms tumor 1
GUncertain significance
GPC3
(S560F +3 more)
Single nucleotide variant
(missense variant)
Wilms tumor 1
GUncertain significance
GPC3
Single nucleotide variant
(intron variant)
Wilms tumor 1
GLikely benign
GPC3
Single nucleotide variant
(synonymous variant)
Wilms tumor 1
GLikely benign
GPC3
Single nucleotide variant
(synonymous variant)
Wilms tumor 1
GLikely benign
GPC3
(D235V +2 more)
Single nucleotide variant
(missense variant)
Wilms tumor 1
GUncertain significance
GPC3
Single nucleotide variant
(synonymous variant)
Wilms tumor 1
GUncertain significance
GPC3
(Q164K +2 more)
Single nucleotide variant
(missense variant)
Wilms tumor 1
GUncertain significance
GPC3
Single nucleotide variant
(intron variant)
Wilms tumor 1
GLikely benign
GPC3
Single nucleotide variant
(synonymous variant)
Wilms tumor 1
GLikely benign
GPC3
(I313V +2 more)
Single nucleotide variant
(missense variant)
Wilms tumor 1
GUncertain significance
GPC3
(R39L)
Single nucleotide variant
(missense variant)
Wilms tumor 1
GUncertain significance
GPC3
(Y248N +2 more)
Single nucleotide variant
(missense variant)
Wilms tumor 1
GUncertain significance
GPC3
(Q94R)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
GUncertain significance
GPC3
Single nucleotide variant
(intron variant)
Wilms tumor 1
GUncertain significance
GPC3
(S97N)
Single nucleotide variant
(missense variant +2 more)
Wilms tumor 1
GUncertain significance
WT1
Single nucleotide variant
(non-coding transcript variant +1 more)
Frasier syndrome
+3 more
GLikely pathogenic
LOC107982234, WT1
(P136L +1 more)
Single nucleotide variant
(missense variant +1 more)
Frasier syndrome
+3 more
GUncertain significance
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Frasier syndrome
+3 more
GLikely benign
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Frasier syndrome
+3 more
GLikely benign
WT1
Deletion
(nonsense +3 more)
Frasier syndrome
+3 more
GPathogenic
WT1
(D106G +14 more)
Single nucleotide variant
(missense variant +1 more)
Frasier syndrome
+3 more
GUncertain significance
WT1
Single nucleotide variant
(intron variant)
Frasier syndrome
+3 more
GLikely benign
LOC107982234, WT1
Duplication
(inframe_insertion +2 more)
Frasier syndrome
+3 more
GUncertain significance
WT1
Single nucleotide variant
(synonymous variant +3 more)
Frasier syndrome
+3 more
GLikely benign
WT1
(T279fs +3 more)
Deletion
(frameshift variant +1 more)
Frasier syndrome
+3 more
GPathogenic
LOC107982234, WT1
(S119L +1 more)
Single nucleotide variant
(missense variant +1 more)
Frasier syndrome
+3 more
GUncertain significance
WT1
Indel
(intron variant)
Frasier syndrome
+3 more
GUncertain significance
WT1
(F196C +10 more)
Single nucleotide variant
(missense variant +2 more)
Frasier syndrome
+3 more
GUncertain significance
LOC107982234, WT1
(G186D +1 more)
Single nucleotide variant
(missense variant +1 more)
Frasier syndrome
+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)
Frasier syndrome
+3 more
GUncertain significance
LOC107982234, WT1
(A66fs)
Deletion
(frameshift variant +1 more)
Frasier syndrome
+3 more
GUncertain significance
WT1
(S333R +9 more)
Single nucleotide variant
(missense variant +2 more)
Frasier syndrome
+3 more
GUncertain significance
WT1
Single nucleotide variant
(synonymous variant +1 more)
Frasier syndrome
+3 more
GLikely benign
WT1
(H111fs +13 more)
Deletion
(frameshift variant +1 more)
Frasier syndrome
+3 more
GUncertain significance
LOC107982234, WT1
(M195V +1 more)
Single nucleotide variant
(missense variant +1 more)
Frasier syndrome
+3 more
GUncertain significance
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Frasier syndrome
+3 more
GLikely benign
LOC107982234, WT1
(Q26E +1 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
(T292R +9 more)
Single nucleotide variant
(missense variant +2 more)
Frasier syndrome
+3 more
GUncertain significance
WT1
(S267A +4 more)
Single nucleotide variant
(missense variant +1 more)
Frasier syndrome
+3 more
GUncertain significance
WT1
(N122S +4 more)
Single nucleotide variant
(missense variant +2 more)
Frasier syndrome
+3 more
GUncertain significance
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