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Links from Gene

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SH3PXD2B
Deletion
not provided
GPathogenic
SH3PXD2B
(R94G)
Single nucleotide variant
(missense variant)
Frank-Ter Haar syndrome
GUncertain significance
SH3PXD2B
(P151L)
Single nucleotide variant
(missense variant)
Frank-Ter Haar syndrome
GUncertain significance
SH3PXD2B
(W189*)
Single nucleotide variant
(nonsense)
Frank-Ter Haar syndrome
GLikely pathogenic
SH3PXD2B
(R84*)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
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