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Links from Gene

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WDR4
(R170L +1 more)
Indel
(missense variant +1 more)
Galloway-Mowat syndrome 6
GLikely pathogenic
WDR4
(S179N +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
WDR4
(A104V +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
WDR4
(Y72H +1 more)
Single nucleotide variant
(missense variant +1 more)
Microcephaly, growth deficiency, seizures, and brain malformations
GUncertain significance
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