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Links from MedGen

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TMEM67
(R360C +1 more)
Single nucleotide variant
(missense variant +1 more)
Meckel syndrome, type 3
+23 more
GConflicting classifications of pathogenicity
TMEM67
(C615R +1 more)
Single nucleotide variant
(missense variant +1 more)
TMEM67-related condition
+27 more
GPathogenic/Likely pathogenic