RS5982 F13A1

Health Risk Chr 6:6174632 snv missense variant

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Associated Conditions

Factor XIII

A subunit

deficiency of

Hereditary factor XIII deficiency disease

Factor XIII

A subunit

deficiency of

Hereditary factor XIII deficiency disease

GWAS Studies (3)

Trait	Risk Allele	OR / Beta	P-value	Study
F13B protein levels	A	β: 0.062	1E-20	PubMed
Serum levels of protein FRS2	A	OR: 0.18	2E-16	PubMed
Height	A	β: 0.005	2E-10	PubMed

Population Frequencies

gnomAD ALL

78.4%

1kG AFR

14.5%

1kG ALL

24%

1kG AMR

10.1%

1kG EAS

35.8%

1kG EUR

78.9%

1kG SAS

37.7%

Other Variants in F13A1