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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129992120, LRPAP1
(R37P)
Single nucleotide variant
(missense variant)
not provided
GBenign
LOC129992120, LRPAP1
Single nucleotide variant
(synonymous variant)
not provided
GBenign
LOC129992120, LRPAP1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LOC129992120, LRPAP1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LOC129992120, LRPAP1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
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