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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRMT7
Single nucleotide variant
(intron variant)
Short stature-brachydactyly-obesity-global developmental delay syndrome
GUncertain significance
PRMT7
(V117M +3 more)
Single nucleotide variant
(missense variant +1 more)
Short stature-brachydactyly-obesity-global developmental delay syndrome
+1 more
GUncertain significance
PRMT7
(R281C +3 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+1 more
GUncertain significance
PRMT7
(E507K +4 more)
Single nucleotide variant
(missense variant +1 more)
Short stature-brachydactyly-obesity-global developmental delay syndrome
GUncertain significance
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