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Links from MedGen

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GMNN
Single nucleotide variant
(synonymous variant)
Meier-Gorlin syndrome 6
GUncertain significance
GMNN
(K17R)
Single nucleotide variant
(missense variant)
Meier-Gorlin syndrome
GLikely pathogenic
GMNN
(I12fs)
Deletion
(frameshift variant)
Meier-Gorlin syndrome
GPathogenic
GMNN
(K6*)
Single nucleotide variant
(nonsense)
Meier-Gorlin syndrome
GPathogenic
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