RS28936381 GFI1

Health Risk Chr 1:92476153
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What This Variant Does
"[OMIM:NEUTROPENIA, CONGENITAL, AUTOSOMAL DOMINANT 2]
Associated Conditions
Neutropenia
severe congenital
2
autosomal dominant
Neutropenia
severe congenital
2
autosomal dominant
Other Variants in GFI1
rs28936382 rs35896485 rs755193129 rs777241871 rs1290770390 rs758542203 rs551351361 rs200577201 rs529448705 rs962841876
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