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Links from MedGen

Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
APC
(P1415S +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
GUncertain significance
APC
(L1545V +12 more)
Single nucleotide variant
(missense variant)
Neoplasm of the liver
GUncertain significance
APC
(Y917C +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
+1 more
GUncertain significance
APC
(R1221K +12 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
APC
(S2781L +12 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
APC
(M508V +12 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
APC
(R787Q +12 more)
Single nucleotide variant
(missense variant)
Classic or attenuated familial adenomatous polyposis
+4 more
GConflicting classifications of pathogenicity
APC
(A2760S +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
+3 more
GConflicting classifications of pathogenicity
APC
(V1125A +12 more)
Single nucleotide variant
(missense variant)
Neoplasm of the liver
+5 more
GConflicting classifications of pathogenicity
APC
(A735V +12 more)
Single nucleotide variant
(missense variant)
Colorectal cancer, susceptibility to
+4 more
GConflicting classifications of pathogenicity
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