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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126807343, PDZD2
(A2677T)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
LOC126807343, PDZD2
(M2708V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC126807343, PDZD2
(R2716W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC126807343, PDZD2
(P2720H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC126807343, PDZD2
(G2726C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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