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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SSX7
(E185K)
Single nucleotide variant
(missense variant)
not provided
GBenign
SSX7
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
SSX7
(T165I)
Single nucleotide variant
(missense variant)
not provided
GBenign
SSX7
Single nucleotide variant
(splice acceptor variant)
not provided
GLikely benign
SSX7
Single nucleotide variant
(intron variant)
not provided
GLikely benign
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