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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GBA1, LOC106627981
(R502C +2 more)
Single nucleotide variant
(missense variant)
Parkinson disease, late-onset
+9 more
GPathogenic
GBA1, LOC106627981
(L483P +2 more)
Single nucleotide variant
(missense variant)
Parkinson disease, late-onset
+15 more
GPathogenic; risk factor
GBA1, LOC106627981
(N409S +2 more)
Single nucleotide variant
(missense variant)
not provided
+13 more
GPathogenic/Likely pathogenic; risk factor
GBA1, LOC106627981
(N227S +2 more)
Single nucleotide variant
(missense variant)
not provided
+8 more
GPathogenic
SNCB
(K34E)
Single nucleotide variant
(missense variant)
Lewy body dementia
GUncertain significance
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