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Items: 8

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PIEZO2
(R2382W +1 more)
Single nucleotide variant
(missense variant)
Arthrogryposis, distal, with impaired proprioception and touch
GUncertain significance
PIEZO2
(T1942M +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
PIEZO2
(D1636N +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
PIEZO2
(R1575Q +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
PIEZO2
(S1431N +1 more)
Single nucleotide variant
(missense variant)
autosomal recessive PIEZO2 associated disease
+1 more
GUncertain significance
PIEZO2
(T1358M +1 more)
Single nucleotide variant
(missense variant)
Arthrogryposis, distal, with impaired proprioception and touch
+2 more
GUncertain significance
PIEZO2
Single nucleotide variant
(splice acceptor variant)
Arthrogryposis, distal, with impaired proprioception and touch
+1 more
GPathogenic
PIEZO2
(V6L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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