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Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CEACAM16, CEACAM16-AS1
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign
CEACAM16-AS1, CEACAM16
(E118K)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign
CEACAM16, CEACAM16-AS1
(G197S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
CEACAM16, CEACAM16-AS1
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign/Likely benign
CEACAM16, CEACAM16-AS1
(T290M)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
CEACAM16, CEACAM16-AS1
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GConflicting classifications of pathogenicity
CEACAM16, CEACAM16-AS1
(D397E)
Single nucleotide variant
(missense variant)
Hearing loss, autosomal recessive 113
+2 more
GUncertain significance
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