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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYO18B
Single nucleotide variant
(synonymous variant)
Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome
+1 more
GBenign/Likely benign
MYO18B
(G415V)
Single nucleotide variant
(missense variant)
Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome
+1 more
GUncertain significance
MYO18B
(P1206S +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
MYO18B
Single nucleotide variant
(intron variant)
Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome
+1 more
GBenign/Likely benign
MYO18B
Single nucleotide variant
(intron variant)
Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome
+1 more
GUncertain significance
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