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Links from MedGen

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WDR73
Deletion
(inframe deletion +1 more)
Galloway-Mowat syndrome
GUncertain significance
GON7
(Y7*)
Single nucleotide variant
(nonsense)
Galloway-Mowat syndrome
GPathogenic
WDR4
Single nucleotide variant
(splice acceptor variant)
Galloway-Mowat syndrome
GLikely pathogenic
ZNF592
(V911I)
Single nucleotide variant
(missense variant)
Galloway-Mowat syndrome 1
GUncertain significance
OSGEP
(R325Q)
Single nucleotide variant
(missense variant)
Galloway-Mowat syndrome
GPathogenic
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