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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FANCL, VRK2
(T372fs +3 more)
Duplication
(frameshift variant +1 more)
FANCL-related condition
+5 more
GConflicting classifications of pathogenicity
FANCL
Deletion
(inframe_indel)
FANCL-related condition
+4 more
GConflicting classifications of pathogenicity
FANCL
(I184del +3 more)
Microsatellite
(inframe_indel +1 more)
Fanconi anemia complementation group L
GUncertain significance
FANCL
(N50fs)
Indel
(frameshift variant)
Fanconi anemia complementation group L
GUncertain significance
FANCL
Indel
(missense variant)
Fanconi anemia
+1 more
GUncertain significance
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