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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHD1L
(R614* +7 more)
Single nucleotide variant
(nonsense +1 more)
not provided
GUncertain significance
CHD1L
(N680K +7 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
CHD1L, LOC126805854
(Q804* +7 more)
Single nucleotide variant
(nonsense +1 more)
not provided
+1 more
GLikely benign
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