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Links from MedGen

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MIA3
(P1726L +5 more)
Single nucleotide variant
(missense variant)
Odontochondrodysplasia 2 with hearing loss and diabetes
GUncertain significance
MIA3
Microsatellite
(intron variant)
Odontochondrodysplasia 2 with hearing loss and diabetes
GUncertain significance