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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CRELD1
(R107H)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
CRELD1
Single nucleotide variant
(synonymous variant +1 more)
not specified
+2 more
GBenign/Likely benign
CRELD1
Single nucleotide variant
(synonymous variant +1 more)
not provided
GUncertain significance
CRELD1
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
GUncertain significance
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