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Links from MedGen

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC30A7
Single nucleotide variant
(intron variant)
Testicular atrophy
GLikely pathogenic
Translocation
Orofacial cleft
+2 more
GPathogenic
PLEKHG5
(P28L +3 more)
Single nucleotide variant
(missense variant)
Testicular atrophy
+4 more
GUncertain significance
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