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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MTTP
Single nucleotide variant
(intron variant)
Abetalipoproteinaemia
GUncertain significance
MTTP
Single nucleotide variant
(splice acceptor variant)
Abetalipoproteinaemia
+1 more
GLikely pathogenic
MTTP
(E777* +1 more)
Single nucleotide variant
(nonsense)
Abetalipoproteinaemia
GPathogenic
MTTP
(P886L +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
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