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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PYGL
(D634H +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
PYGL
Single nucleotide variant
(splice donor variant)
Glycogen storage disease, type VI
GPathogenic
PYGL
Single nucleotide variant
(synonymous variant)
Glycogen storage disease, type VI
GUncertain significance
PYGL
(N225K +1 more)
Single nucleotide variant
(missense variant)
Glycogen storage disease, type VI
GUncertain significance
PYGL
(R209H +1 more)
Single nucleotide variant
(missense variant)
Glycogen storage disease, type VI
GUncertain significance
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