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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LCT
Single nucleotide variant
(intron variant)
not provided
+1 more
GUncertain significance
LCT
(Q1179*)
Single nucleotide variant
(nonsense)
Congenital lactase deficiency
+1 more
GPathogenic
LCT
(D905G)
Single nucleotide variant
(missense variant)
Lactose intolerance
+2 more
GBenign/Likely benign
LCT
(A152T)
Single nucleotide variant
(missense variant)
Lactose intolerance
+2 more
GBenign/Likely benign
LCT
(A94T)
Single nucleotide variant
(missense variant)
Congenital lactase deficiency
+1 more
GUncertain significance
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