Endpoint · lookupGETsaylorinnovations.com/api/bio/variant/rs334

Genetic Variant Clinical Significance (ClinVar).

Genetic Variant Clinical Significance (ClinVar). Genetic variant clinical significance from ClinVar by rsID, ClinVar id (VCV) or HGVS: pathogenic / benign / uncertain classification, review status with 0-4 stars, conditions, genes, molecular consequence, protein change and last evaluated date, best-reviewed record first. NCBI ClinVar, public domain; not medical advice.

UNRATEDListed

Overview

Grade?

UNRATED

0 of 30 paid calls toward a letter

Price

$0.003 per call

Paid calls

none yet

delivery unknown until someone pays

More info

Seller?

7lsjfrjf8f…yuvxacy7

URL

https://saylorinnovations.com/api/bio/variant/rs334

MCP server on this host: com.saylorinnovations/data

Seen

first 8 days ago · last 11 hr ago

12 free handshakes

Payment

Pays through

x402

Offered on?

Polygon, Arbitrum, Base, Solana USDC

Listed on?

Polygon, Arbitrum, Base, Solana

Handshakescomputed 17 hr ago

0.241 from 12 free handshakes over 30 days · UNRATED ?

How the composite of 0.241 is made up, part by part
Component	Weight	Measured	Lower bound ?		Adds	Short ?	Uncertain ?
livenesscosts the most it answered at all	0.60	0.62	0.068		0.041	−0.226	−0.333
latency p95 it answered as fast as its class	0.20	0.00	0.000		0.000	−0.200	0
price stability the price stayed where it was listed	0.20	1.00	1.000		0.200	0	0
Composite	1.00		0.241	gap to 1.000 = 0.759 · 0.426 short · 0.333 uncertain	0.241	−0.426	−0.333

Not measured: correctness · nobody paid; honesty · nobody paid; schema conformance · no answer had a published shape to check

BURN_INFREE_TIER_ONLY

Verify it yourselfnpx teppi-check https://saylorinnovations.com/api/bio/variant/rs334curl -s https://api.teppi.xyz/v1/trust/cap_01M3E3X0RMASZPDY9P86NQCKT7