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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BMPR1A
(P2T)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+4 more
GBenign
BMPR1A
(F146S)
Single nucleotide variant
(missense variant)
Polyposis syndrome, hereditary mixed, 2
+3 more
GConflicting classifications of pathogenicity
BMPR1A
(Y318C)
Single nucleotide variant
(missense variant)
Juvenile polyposis syndrome
+5 more
GConflicting classifications of pathogenicity
BMPR1A
(E415K)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
BMPR1A
(R443C)
Single nucleotide variant
(missense variant)
not provided
+5 more
GConflicting classifications of pathogenicity
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