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Links from MedGen

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
F9
(V228L +1 more)
Single nucleotide variant
(missense variant)
Hemophilia b(m)
GPathogenic
F9
(R226Q +1 more)
Single nucleotide variant
(missense variant)
Hereditary factor IX deficiency disease
GPathogenic