NIPT prenatal DNA test cost in Valdosta, GA
In Valdosta, GA, 2 hospitals list a cash price for prenatal cell-free DNA screen for trisomy 21, 18 and 13 (NIPT): from $967.50 to $967.50, with a median of $967.50. The lowest listed price is at South Georgia Medical Center Lanier Campus and 1 other hospital. Across Georgia, the median is $967.50 at 11 hospitals.
Cash prices at 2 facilities across 2 cities for code 81420, as an outpatient — the setting a self-pay patient normally buys. Collected Sep 27, 2026; the hospital files themselves were last updated between — and —.
Where each hospital's price falls
Each dot is one hospital's cash price on a scale from the lowest to the highest in Valdosta, GA.
Hospitals, cheapest first
| Hospital | Cash price | List price | Insurers pay | Off list | File date |
|---|---|---|---|---|---|
| South Georgia Medical Center Lanier Campus lowest Lakeland, GA · (229) 482-8402 FETAL CHRMOML ANEUPLOIDY | $967.50 | $1,290.00 | $759.05–$1,138.58 | 25% | — source file |
| South Georgia Medical Center lowest Valdosta, GA · (229) 333-1020 FETAL CHRMOML ANEUPLOIDY | $967.50 | $1,290.00 | $603.44–$986.76 | 25% | — source file |
Outpatient: lowest $967.50, median $967.50, highest $967.50.
Cash or insurance?
At 2 of 2 hospitals that publish insurer rates for this code here, the cash price is below the highest rate a health plan has negotiated, and at none is it below every plan's rate. If you have insurance but have not met your deductible, you usually pay your plan's negotiated rate, which falls somewhere in the "Insurers pay" column. Paying cash can cost less, but a cash payment usually does not count toward your deductible. Ask the hospital for both numbers before you book.
What it is
NIPT analyzes fragments of fetal DNA that circulate in the mother's blood to screen for Down syndrome (trisomy 21) and trisomies 18 and 13. It can be done from about 10 weeks of pregnancy. It is a screening test, so a positive result needs a diagnostic test to confirm.
What the price covers
The price usually covers the DNA analysis of one blood sample. The blood draw, genetic counseling and any added screens, such as sex chromosomes or microdeletions, may be billed separately.