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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC128092249, PCNT
Single nucleotide variant
(intron variant)
not provided
+1 more
GConflicting classifications of pathogenicity
LOC128092249, PCNT
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
+2 more
GConflicting classifications of pathogenicity
LOC128092249, PCNT
(D47H)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
+3 more
GUncertain significance
LOC128092249, PCNT
(A48P)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
+1 more
GBenign
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