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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PGM3
(L480I +2 more)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
+2 more
GUncertain significance
PGM3
(R169Q +2 more)
Single nucleotide variant
(missense variant +1 more)
Immunodeficiency 23
GUncertain significance
PGM3
(R29Q +1 more)
Single nucleotide variant
(missense variant +2 more)
Immunodeficiency 23
GUncertain significance
PGM3
(H13R +1 more)
Single nucleotide variant
(missense variant +2 more)
Immunodeficiency 23
GUncertain significance
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