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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RFWD3
Single nucleotide variant
(synonymous variant)
Fanconi anemia, complementation group W
+1 more
GLikely benign
RFWD3
(C178S +1 more)
Single nucleotide variant
(missense variant)
Fanconi anemia, complementation group W
GUncertain significance
RFWD3
(V119L +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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