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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RETREG1
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
RETREG1
Single nucleotide variant
(synonymous variant)
RETREG1-related condition
+2 more
GConflicting classifications of pathogenicity
LOC129993734, RETREG1
+1 more
Single nucleotide variant
(5 prime UTR variant)
Neuropathy, hereditary sensory and autonomic, type 2B
+1 more
GBenign
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