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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HBB, LOC107133510
+1 more
(E122K)
Single nucleotide variant
(missense variant)
Sickle cell-Hemoglobin O Arab disease
+11 more
GPathogenic/Likely pathogenic
HBB, LOC106099062
+1 more
(E7V)
Single nucleotide variant
(missense variant)
HBB-related disorder
+15 more
GPathogenic