In addition to personal genome sequencing, there are many genetic tests available for individual diseases and conditions.

You should read the genetic ethics section as an additional step along with consulting your doctor before you order any specific DNA tests.

Tests exist for assessing risk of blood clotting disorders, breast cancer, celiac disease, colon cancer, cystic fibrosis, diabetes, hemochromatosis, hemophilia, huntington disease, infertility, ovarian cancer, pregnancy loss, sickle cell anemia, and many other conditions. See below:

Other Conditions

Alpha-1 Antitrypsin Deficiency

Angelman Syndrome

Ashkenazi Jewish Panel

Asperger Syndrome

Ataxia Panel

Becker Muscular Dystrophy

Bloom Syndrome

CADASIL

Canavan Disease

Celiac Disease

Charcot-Marie-Tooth Disease

Congenital Bilateral Absence of the Vas Deferens (CBAVD)

Deafness Panel

Dentatorubral-Pallidoluysian Atrophy (DRPLA)

DNA Banking

Duchenne Muscular Dystrophy

Factor V Leiden

Familial Adenomatous Polyposis

Familial Dysautonomia

Familial Mediterranean Fever

Fanconi Anemia

Fragile X Syndrome

Friedreich Ataxia

Gaucher Disease

Glaucoma

Hemophilia

Huntington Disease

Kennedy Disease (SBMA)

Lymphoblast Banking

Medium-Chain ACYL-COA Dehydrogenase (MCAD)

Methylenetetrahydrofolate Reductase (MTHFR)

Microarray SNP-CHIP

Mitochondrial Disorders

Multiple Endocrine Neoplasia

Myotonic Muscular Dystrophy

Neurofibromatosis

Neuroligin

Niemann-Pick Disease

Paraganglioma

Paternity

Pendred Syndrome

Phenylketonuria

Philadelphia Chromosome

Prader-Willi

Prothrombin

Rett Syndrome

Smith-Lemli-Opitz Syndrome (SLOS)

Spinal Muscular Atrophy

Tay-Sachs Disease

Thalassemia

Thrombophilia

Tuberous Sclerosis

Uniparental Disomy

Von-Hippel-Lindau

Waardenburg Syndrome

Wilson Disease

X-Linked Lymphoproliferative Disease (XLP)

Zygosity