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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
C1QA
(E23K)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign/Likely benign
C1QA
(L91F)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
C1QA
Single nucleotide variant
(synonymous variant)
not provided
GBenign/Likely benign
C1QA
(N194T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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