Invest in BillionToOne, Inc. Class A on Stash
BillionToOne Inc is a United States-based precision diagnostics company. The Company provides Quantitative Counting Template (QCT) molecular counter platform, is the only technology platform that can count deoxyribonucleic acid (DNA) molecules to the single-count level and detect risk for common and severe genetic diseases.
Ticker: BLLN
BillionToOne, Inc. Class A
$91.94
+11.43%
$
BLLN Performance Breakdown
Share Price
$91.94
Today's change
-0.51%
Year to date change (YTD)
2.97%
Dividend yield
0.0
Last dividend paid
N/A
Last dividend pay date
N/A
About BLLN
BillionToOne Inc is a United States-based precision diagnostics company. The Company provides Quantitative Counting Template (QCT) molecular counter platform, is the only technology platform that can count deoxyribonucleic acid (DNA) molecules to the single-count level and detect risk for common and severe genetic diseases. The Company’s product UNITY, is a noninvasive prenatal screening that tests fetal cell-free DNA for cystic fibrosis (CF) and spinal muscular atrophy (SMA) through a single sample of the mother's blood.
BillionToOne, Inc. Class A Stock Ticker
BLLN
For more information
Invest in BillionToOne, Inc. Class A on Stash
BillionToOne Inc is a United States-based precision diagnostics company. The Company provides Quantitative Counting Template (QCT) molecular counter platform, is the only technology platform that can count deoxyribonucleic acid (DNA) molecules to the single-count level and detect risk for common and severe genetic diseases.
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BillionToOne, Inc. Class A stock news
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Once your market order of BillionToOne, Inc. Class A stock is complete, you'll officially be a shareholder of BillionToOne, Inc. Class A!
Invest in BillionToOne, Inc. Class A on Stash
BillionToOne Inc is a United States-based precision diagnostics company. The Company provides Quantitative Counting Template (QCT) molecular counter platform, is the only technology platform that can count deoxyribonucleic acid (DNA) molecules to the single-count level and detect risk for common and severe genetic diseases.



