RS777966677 JAGN1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Severe congenital neutropenia
Autosomal recessive severe congenital neutropenia due to JAGN1 deficiency
Severe congenital neutropenia
Autosomal recessive severe congenital neutropenia due to JAGN1 deficiency
Other Variants in JAGN1