RS121909625 FGB

Health Risk Chr 4:154565832
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What This Variant Does
"[OMIM:?]
Associated Conditions
Congenital afibrinogenemia
Hypofibrinogenemia
Afibrinogenemia
Congenital afibrinogenemia
Hypofibrinogenemia
Afibrinogenemia
Other Variants in FGB
rs770246669 rs1578785111 rs1578783532 rs187641148 rs111502670 rs1282469317 rs1730132238 rs2530766247 rs2530775972 rs149599496
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