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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
C1S
(S34G)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GUncertain significance
C1S
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GLikely benign
C1S
(V160L +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GLikely benign
C1S
(R534W +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
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