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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ELP1
(R1198* +2 more)
Single nucleotide variant
(nonsense)
Familial dysautonomia
+3 more
GPathogenic/Likely pathogenic
ELP1
(H949Y +2 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
ELP1
(V92I)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
+2 more
GUncertain significance
ELP1
(R2*)
Single nucleotide variant
(5 prime UTR variant +2 more)
Familial dysautonomia
+2 more
GPathogenic/Likely pathogenic
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