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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC112529895, SCO1
(G56E)
Single nucleotide variant
(missense variant)
SCO1-related condition
+2 more
GBenign/Likely benign
LOC112529895, SCO1
Single nucleotide variant
(synonymous variant)
SCO1-related condition
GLikely benign
LOC112529895, SCO1
(P14L)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
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