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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ALAS2, LOC108663984
(S105N)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ALAS2, LOC108663984
(V120A +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ALAS2, LOC108663984
(F33S +1 more)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
ALAS2, LOC108663984
(V13M +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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