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Links from MedGen

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NPR2
Deletion
(intron variant)
Acromesomelic dysplasia
+2 more
GBenign
GDF5, LOC109461476
Single nucleotide variant
(5 prime UTR variant)
Symphalangism-brachydactyly syndrome
+4 more
GUncertain significance