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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RSPO2
Single nucleotide variant
(synonymous variant)
RSPO2-related disorder
+1 more
GLikely benign
RSPO2
(H149L +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GLikely benign
LOC124174315, RSPO2
Single nucleotide variant
(synonymous variant)
RSPO2-related disorder
GLikely benign
LOC124174315, RSPO2
Single nucleotide variant
(5 prime UTR variant)
RSPO2-related disorder
GLikely benign
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