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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHD1L, LOC129931354
(M1L)
Single nucleotide variant
(5 prime UTR variant +4 more)
not provided
+1 more
GLikely benign
CHD1L, LOC129931354
(S8I)
Single nucleotide variant
(5 prime UTR variant +3 more)
CHD1L-related disorder
GLikely benign
CHD1L, LOC129931354
Single nucleotide variant
(5 prime UTR variant +3 more)
CHD1L-related disorder
GLikely benign
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