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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRMT7
(V117M +3 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
PRMT7
(R418Q +3 more)
Single nucleotide variant
(missense variant +2 more)
Short stature-brachydactyly-obesity-global developmental delay syndrome
+1 more
GUncertain significance