RS139164988 F13A1

Health Risk Chr 6:6224748
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Associated Conditions
Factor XIII
A subunit
deficiency of
Inborn genetic diseases
Factor XIII
A subunit
deficiency of
Inborn genetic diseases
Other Variants in F13A1
rs2113184331 rs121913064 rs121913065 rs121913066 rs121913067 rs121913069 rs121913070 rs121913071 rs5985 rs121913072
Ask Dr. Hemsworth about this variant