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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATXN7, LOC129936979
Single nucleotide variant
(synonymous variant)
ATXN7-related condition
GLikely benign
ATXN7, LOC108660406
+1 more
Microsatellite
(inframe_insertion +1 more)
ATXN7-related condition
GLikely benign
ATXN7, LOC108660406
+1 more
(Q35P)
Single nucleotide variant
(missense variant)
ATXN7-related condition
GLikely benign
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