NCBI dbSNP short variant record by rs number: variant type
health_dbSNP_polymorphismsNCBI dbSNP short variant record by rs number: variant type, placement (sequence and position), reference and alternate sequence, and study allele frequencies (e.g. 1000 Genomes allele counts). Up to 10 frequency rows per call. Price: $0.002 in USDC per successful call, paid with x402 (Base, Solana or Arc); failed calls are not charged.
Tool call template
Replace each placeholder with a value matching the input schema. Only required parameters are included; add optional parameters as needed.
{
"id": 1,
"jsonrpc": "2.0",
"method": "tools/call",
"params": {
"arguments": {
"rsid": "<rsid>"
},
"name": "health_dbSNP_polymorphisms"
}
}Input Schema
| Name | Required | Description | Default |
|---|---|---|---|
| rsid | Yes | dbSNP rs number, e.g. rs429358 |
Output Schema
| Name | Required | Description | Default |
|---|---|---|---|
| rsid | No | ||
| source | No | ||
| checkedAt | No | ||
| placement | No | ||
| frequencies | No | ||
| variantType | No |