RS587777730 JAGN1

Health Risk Chr 3:9893310
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive severe congenital neutropenia due to JAGN1 deficiency
Severe congenital neutropenia
Autosomal recessive severe congenital neutropenia due to JAGN1 deficiency
Severe congenital neutropenia
Other Variants in JAGN1
rs587777727 rs587777728 rs587777729 rs587777731 rs786205704 rs777966677 rs786205705 rs748123071 rs200485958 rs755763965
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