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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EGLN1
(A96V)
Single nucleotide variant
(missense variant)
Erythrocytosis, familial, 3
+1 more
GConflicting classifications of pathogenicity
EGLN1
Single nucleotide variant
(synonymous variant)
Hemoglobin, high altitude adaptation
+3 more
GBenign/Likely benign
EGLN1
(S14N)
Single nucleotide variant
(missense variant)
Erythrocytosis, familial, 3
+2 more
GUncertain significance
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