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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FANCL, VRK2
(T372fs +3 more)
Duplication
(frameshift variant +1 more)
Fanconi anemia
+4 more
GConflicting classifications of pathogenicity
FANCL
Single nucleotide variant
(synonymous variant)
Fanconi anemia complementation group L
+1 more
GPathogenic
FANCL
(H244Y +3 more)
Single nucleotide variant
(missense variant)
Fanconi anemia complementation group L
GUncertain significance
FANCL
(N19S)
Single nucleotide variant
(missense variant)
Fanconi anemia complementation group L
GUncertain significance
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