Important Shipping Restriction: We are currently unable to ship to Rhode Island, Pennsylvania, Maryland, New Jersey, or New York. If your shipping address is in one of these states, please do not place an order at this time. STI/Pap Smear Alternative HPV Screening | At-Home Collection Kit Screen for three of the most common sexually transmitted infections from the privacy of home. This kit tests for Chlamydia, Gonorrhea, Mycoplasma genitalium, Trichomoniasis, pap smear alternative (high risk genotype screen for 8 of the most common high risk HPV strains), HSV1, and HSV2, using NAATs (nucleic acid amplification tests). This kit uses a first void urine collection kit initially designed to use as a non-invasive HPV testing pap smear alternative. This is recommended instead of a pap smear every 5 years for women aged 30-65 by many patient advocacy groups. Pathogens screened: Chlamydia Gonorrhea Mycoplasma genitalium Trichomoniasis HPV (16, 18, 31, 33, 45, 52, 58, 67) high-risk genotype testing (16, 18, 31, 45, and 33/52/58/67) Herpes Simplex Virus 1 (HSV-1) Herpes Simplex Virus 2 (HSV-2) Sample type: First-void urine What's included: Free 2-business day shipping · First void urine collection tube · First void urine collection funnel · Lesion swab collection tube with preservative · 3 swabs · gloves · Two pre-paid 2-business day return shipping envelopes (so you can select optimal timing for lesion swabs if HSV infection is suspected) · Clinician-authorized test order · 2 specimen collection bags with absorbent pads · Secure online results 1-3 business days after sample receipt How it works: Purchase your kit Register online - a licensed clinician reviews and authorizes your order Collect your first void urine or lesion swab specimen following the included instructions Ship your sample in the pre-paid mailer Receive your results securely online About your results timeline: Average TAT for 2026 is currently ~18 hours once we receive your sample. Samples received on Friday may take up to 4 days for processing as we do not test on the weekend. The most common reason a sample fails to arrive at our facility is that we primarily use UPS, so please make sure to drop it off at a UPS pickup location, and not at the local post office unless otherwise indicated! About our laboratory: CLIA-certified · California License CLF-90008896 · CLIA ID# 05D2278233 Laboratory Developed Test (LDT): This test was designed, validated, and is performed exclusively at Genome-Based Diagnostics' CLIA-compliant high complexity laboratory (CLIA ID# 05D2278233). LDTs are tests developed and used within a single certified laboratory rather than manufactured for distribution. This test has not undergone FDA premarket review, and its performance characteristics were determined by Genome-Based Diagnostics, meeting or exceeding all applicable CLIA LDT requirements. This is a laboratory screening test processed in our CLIA-compliant facility. A positive screening result should be confirmed by a licensed healthcare provider. Results are not a substitute for clinical evaluation or medical advice.
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