U.S. flag

An official website of the United States government

Format
Sort by
Choose Destination

Search results

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLX4
(C1805R)
Single nucleotide variant
(missense variant)
Fanconi anemia
+2 more
GUncertain significance
SLX4
(T1475A)
Single nucleotide variant
(missense variant)
Malignant tumor of breast
GUncertain significance
SLX4
(P975L)
Single nucleotide variant
(missense variant)
Fanconi anemia complementation group P
+3 more
GBenign/Likely benign
SLX4
(A774S)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
SLX4
(G141W)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
Format
Sort by
Choose Destination