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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TGM6
(M58V)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign
TGM6
(D510H)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
TGM6
(L517W)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
TGM6
Microsatellite
(intron variant)
Spinocerebellar ataxia type 35
GBenign
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