Lab tests CPT 81420 Inpatient — admitted to hospital

NIPT prenatal DNA test cost in Rochester, NY — inpatient

In Rochester, NY, 4 hospitals list a cash price for prenatal cell-free DNA screen for trisomy 21, 18 and 13 (NIPT) as an inpatient: from $2,113.85 to $2,601.66, with a median of $2,113.85. The lowest listed price is at Newark-Wayne Community Hospital and 2 other hospitals. Across New York, the median is $831.00 at 38 hospitals.

Cash prices at 4 facilities across 3 cities for code 81420, as an inpatient (admitted to hospital) . Collected Sep 23, 2026; the hospital files themselves were last updated between Apr 1, 2026 and Apr 1, 2026.

Lowest$2,113.85Newark-Wayne Community Hospital + 2 more
Median$2,113.85half pay less
Highest$2,601.66in this market
Difference1.2×highest vs lowest

Where each hospital's price falls

Each dot is one hospital's cash price on a scale from the lowest to the highest in Rochester, NY.

median
Lowest $2,113.85Highest $2,601.66

Hospitals, cheapest first

HospitalCash price List priceInsurers payOff listFile date
Newark-Wayne Community Hospital lowest Newark, NY · (315) 332-2022 HC FETAL CHROMOSOMAL ANEUPLOIDY GENOMIC SEQ ANALYS $2,113.85 $3,252.07 — 35% Apr 1, 2026
source file
Rochester General Hospital lowest Rochester, NY · (585) 922-4000 HC FETAL CHROMOSOMAL ANEUPLOIDY GENOMIC SEQ ANALYS $2,113.85 $3,252.07 — 35% Apr 1, 2026
source file
Clifton Springs Hospital And Clinic lowest Clifton Springs, NY · (315) 462-9561 HC FETAL CHROMOSOMAL ANEUPLOIDY GENOMIC SEQ ANALYS $2,113.85 $3,252.07 — 35% Apr 1, 2026
source file
The Unity Hospital of Rochester Rochester, NY · (585) 723-7000 HC FETAL CHROMOSOMAL ANEUPLOIDY GENOMIC SEQ ANALYS $2,601.66 $3,252.07 — 20% Apr 1, 2026
source file

Inpatient: lowest $2,113.85, median $2,113.85, highest $2,601.66 — a 1.2× difference within the same market.

As an outpatient, the same code is billed by 8 facilities here, median $1,643.93 — that is the price to compare if you are not being admitted.

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.