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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RELB
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
RELB
Single nucleotide variant
(splice donor variant)
not provided
GLikely pathogenic
RELB
(T494M)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
RELB
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign/Likely benign
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