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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CR2, LOC126805994
Single nucleotide variant
(synonymous variant)
Immunodeficiency, common variable, 7
+1 more
GLikely benign
CR2, LOC126805994
(R360Q)
Single nucleotide variant
(missense variant)
not specified
+2 more
GUncertain significance
CR2, LOC126805994
(M380I)
Single nucleotide variant
(missense variant)
Immunodeficiency, common variable, 7
+1 more
GConflicting classifications of pathogenicity
CR2, LOC126805994
Single nucleotide variant
(synonymous variant)
CR2-related condition
+1 more
GLikely benign
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