Cytochrome P450 2A6 (CYP2A6) Genotyping
Behçet’s disease (Behcet syndrome)
ATN1 (Atrophin 1) Gene Mutation Analysis
Polycystic ovary syndrome
p16 by Immunohistochemistry (CINtec® Histology)
Friedreich Ataxia, Frataxin, Quantitative, Blood
Antibody Identification, Erythrocytes
Cytology, Non-gynecologic
Chlordiazepoxide, Serum
Chloride, 24 Hour, Urine

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/9p21 Genotype (CVD Risk Genotype Test)

All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References

All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References

9p21 Genotype (CVD Risk Genotype Test)
Medical Test

Access to 9p21 Genotype (CVD Risk Genotype Test) is restricted.