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Links from MedGen

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SYT14
(P131R +3 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GUncertain significance
SYT14
(E270del +3 more)
Microsatellite
(inframe_deletion +1 more)
not provided
+2 more
GConflicting classifications of pathogenicity
SYT14
Single nucleotide variant
(synonymous variant +1 more)
not provided
+1 more
GBenign
SYT14
(G484D +3 more)
Single nucleotide variant
(missense variant +1 more)
Autosomal recessive spinocerebellar ataxia 11
GPathogenic
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