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Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LTBP2
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign/Likely benign
LTBP2
(D1310N)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LTBP2
Single nucleotide variant
(synonymous variant)
not specified
+5 more
GBenign
LTBP2
Single nucleotide variant
(intron variant)
not provided
+1 more
GConflicting classifications of pathogenicity
LTBP2
Single nucleotide variant
(intron variant)
Glaucoma 3, primary infantile, B
+5 more
GUncertain significance
LTBP2
(F395L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LTBP2
(R37M)
Single nucleotide variant
(missense variant)
not provided
+3 more
GBenign/Likely benign
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