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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130009573, RFXAP
(M1T)
Single nucleotide variant
(missense variant +1 more)
MHC class II deficiency
GUncertain significance
LOC130009574, RFXAP
(T140I)
Single nucleotide variant
(missense variant)
MHC class II deficiency
GUncertain significance