Chain398: Congenital disorders of glycosylation type 1G

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
ALG12chr22:50304114,chr22:50301430

Qualitative

Type

text

Possible responses

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