RS75848804 FGG

Health Risk Chr 4:154604995
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What This Variant Does
"[OMIM:?]
Associated Conditions
Hereditary spastic paraplegia 4
Congenital afibrinogenemia
Familial dysfibrinogenemia
Hereditary spastic paraplegia 4
Congenital afibrinogenemia
Familial dysfibrinogenemia
Other Variants in FGG
rs121913087 rs121913088 rs121913091 rs2066862 rs587776837 rs587776838 rs6063 rs587776839 rs191297318 rs1553965519
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