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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PGM3
(I350T +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
PGM3
(K189R +2 more)
Single nucleotide variant
(missense variant +1 more)
Immunodeficiency 23
GUncertain significance
PGM3
(R202L +2 more)
Single nucleotide variant
(missense variant +1 more)
Immunodeficiency 23
+1 more
GConflicting classifications of pathogenicity
PGM3
Single nucleotide variant
(synonymous variant +2 more)
Immunodeficiency 23
GConflicting classifications of pathogenicity
PGM3
(Q16K)
Single nucleotide variant
(missense variant +1 more)
Immunodeficiency 23
GUncertain significance
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