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Links from MedGen

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CUL9
(P911L)
Single nucleotide variant
(missense variant)
Psoriasiform dermatitis
+14 more
GUncertain significance
CUL9
(R2413W)
Single nucleotide variant
(missense variant)
Psoriasiform dermatitis
+14 more
GUncertain significance
MYLIP
(H325fs)
Deletion
(frameshift variant)
Coronary artery atherosclerosis
GUncertain significance
ZHX3
(D750V)
Single nucleotide variant
(missense variant)
ZHX3-related condition
+2 more
GConflicting classifications of pathogenicity
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