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Links from MedGen

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FCGR3A
(F21S)
Single nucleotide variant
(intron variant +1 more)
not provided
+1 more
GUncertain significance
FCGR3A
(G49R +3 more)
Single nucleotide variant
(missense variant)
Autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity
GUncertain significance
FCGR3A
Single nucleotide variant
(synonymous variant)
Autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity
GUncertain significance
FCGR3A
(L66H +3 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GUncertain significance
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