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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CR2
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign/Likely benign
CR2
Single nucleotide variant
(synonymous variant)
Immunodeficiency, common variable, 7
+1 more
GLikely benign
CR2
(H669R)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
CR2
Single nucleotide variant
(synonymous variant)
Immunodeficiency, common variable, 7
+2 more
GBenign/Likely benign
CR2
(V871L +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GLikely benign
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