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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC34A3
(N164D)
Single nucleotide variant
(missense variant)
Autosomal recessive hypophosphatemic bone disease
GUncertain significance
SLC34A3
(M176I)
Single nucleotide variant
(missense variant)
Autosomal recessive hypophosphatemic bone disease
GUncertain significance
SLC34A3
(G419D)
Single nucleotide variant
(missense variant)
Autosomal recessive hypophosphatemic bone disease
GLikely pathogenic
SLC34A3
(T425A)
Single nucleotide variant
(missense variant)
Autosomal recessive hypophosphatemic bone disease
GUncertain significance
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