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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129996890, PREP
(T14I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC129996890, PREP
(E13D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC129996890, PREP
(V9M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PREP, LOC129996890
(D8E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC129996890, PREP
(L4F)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
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