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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129930568, LRP8
Insertion
(inframe insertion)
LRP8-related disorder
GLikely benign
LOC129930568, LRP8
(Q25L)
Single nucleotide variant
(missense variant)
LRP8-related disorder
GLikely benign
LOC129930568, LRP8
Microsatellite
(inframe_insertion)
LRP8-related disorder
+1 more
GBenign/Likely benign
LOC129930568, LRP8
Single nucleotide variant
(5 prime UTR variant)
LRP8-related disorder
GLikely benign
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