RS121907948 SERPING1
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What This Variant Does
"[OMIM:?]
Associated Conditions
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor
Hereditary angioedema type 1
Inborn genetic diseases
C1 inhibitor deficiency
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor
Hereditary angioedema type 1
Inborn genetic diseases
C1 inhibitor deficiency
Other Variants in SERPING1