U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MAFB
(A288V)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
MAFB
(T232A)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
MAFB
(H193P)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
MAFB
(H193Y)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+3 more
GUncertain significance
MAFB
(H165R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
MAFB
(V150M)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
MAFB
(P146L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
MAFB
(A130V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
MAFB
(S123T)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
MAFB
(E98D)
Single nucleotide variant
(missense variant)
Multicentric carpo-tarsal osteolysis with or without nephropathy
+3 more
GConflicting classifications of pathogenicity
MAFB
(S70L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely pathogenic
MAFB
(E19Q)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign/Likely benign
Format
Items per page
Sort by
Choose Destination