Chain496: Deficiency of Factor XIII, A Subunit

This is a rare disease.

Example use A

Rare disease screening of newborns or adults thinking of having children. Could also be used as part of a comprehensive analysis of a person's genes.

Developer

Dr. Colby

Genetic info

GenesGenetic variants
F13A1chr6:6224943,chr6:6175056,chr6:6152107

Qualitative

Type

text

Possible responses

Carrier, Possibly Affected, Not Detected, insufficient data, error