RS2815822 F13A1

Health Risk Chr 6:6320574 snv intron variant

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What This Variant Does

"CLNSIG=5

Associated Conditions

Factor XIII

A subunit

deficiency of

Factor XIII

A subunit

deficiency of

ClinVar Assertions (1)

NM_000129.4(F13A1):c.-19+12=

· 1 submitter

Population Frequencies

gnomAD ALL

13.5%

1kG AFR

11.6%

1kG ALL

88.2%

1kG AMR

88.6%

1kG EAS

5.3%

1kG EUR

89.3%

1kG SAS

79.9%

Other Variants in F13A1