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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HEXA
(R499H +1 more)
Single nucleotide variant
(missense variant +1 more)
Tay-Sachs disease
+2 more
GPathogenic
HEXA
(W420fs +1 more)
Deletion
(frameshift variant)
Tay-Sachs disease
GPathogenic
HEXA
(R178H +1 more)
Single nucleotide variant
(missense variant +1 more)
Tay-Sachs disease
+3 more
GPathogenic/Likely pathogenic
HEXA
(R170W +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GPathogenic/Likely pathogenic
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