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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HADHB
Duplication
(inframe_insertion +1 more)
not specified
+1 more
GBenign
HADHB
Single nucleotide variant
(synonymous variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
HADHB
(R282C +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
HADHB
Single nucleotide variant
(intron variant)
not specified
+1 more
GBenign
HADHB
(G427E +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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