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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KMT2A
(P425fs)
Deletion
(frameshift variant)
Wiedemann-Steiner syndrome
GPathogenic
KMT2A
(S996P)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
KMT2A
(Q1816* +1 more)
Single nucleotide variant
(nonsense)
Wiedemann-Steiner syndrome
GPathogenic
KMT2A
(R2163* +1 more)
Single nucleotide variant
(nonsense)
Inborn genetic diseases
+2 more
GPathogenic
KMT2A
(S3106fs +2 more)
Deletion
(frameshift variant)
Wiedemann-Steiner syndrome
GPathogenic
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