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Links from OMIM

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RHCE
(H172fs +2 more)
Indel
(frameshift variant +1 more)
RH-NULL, AMORPH TYPE
GPathogenic
EPB42
(E583* +1 more)
Single nucleotide variant
(nonsense)
Hereditary spherocytosis type 5
GPathogenic