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Links from MedGen

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NEK1
(S155T)
Single nucleotide variant
(missense variant +1 more)
Mohr syndrome
GPathogenic
Short-rib thoracic dysplasia 6 with or without polydactyly
GPathogenic
INTU
(N132fs)
Deletion
(frameshift variant)
Mohr syndrome
+1 more
GPathogenic/Likely pathogenic
NEK1
(W409* +1 more)
Single nucleotide variant
(nonsense +2 more)
Short-rib thoracic dysplasia 6 with or without polydactyly
+1 more
GPathogenic/Likely pathogenic
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