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Links from MedGen

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MTM1
(R421L +1 more)
Single nucleotide variant
(missense variant)
not provided
+14 more
GPathogenic/Likely pathogenic
BICD2
(N546del)
Deletion
(inframe_deletion)
not provided
+15 more
GPathogenic/Likely pathogenic
Translocation
Epicanthus
+28 more
GUncertain significance
KCNQ1
(K362R +2 more)
Single nucleotide variant
(missense variant)
Congenital long QT syndrome
+22 more
GPathogenic/Likely pathogenic
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