Genomic Report ReaderVCF · 23andMe · CSV · TSVUpload → PGx findings in <60 seconds

Drop a genomic report. Get an India-calibrated PGx safety report.

Upload a VCF from your NGS pipeline, a raw 23andMe export, or a CSV with rsID + genotype columns. We extract the actionable PGx variants — CYP2C19, NUDT15, TPMT, G6PD, CYP2D6, CYP2C9, VKORC1, HLA-B*57:01, DPYD, SLCO1B1, MTHFR, ABCB1 — cross-referenced against IndiGen frequencies and CPIC-graded dosing guidance. Sub-200ms per variant. Audit-logged.

Positioning: Decision support. Not a diagnostic. Every prescribing decision remains the treating clinician's responsibility. Live data state at /methods.

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Drop your genomic report here

or click to browse — VCF · 23andMe .txt · CSV · TSV · 25 MB max

Supported file formats

VCF

.vcf

Standard NGS pipeline output. Requires ##fileformat=VCF header. Genotype extracted from the GT field of the sample column.

23andMe raw export

.txt

4 tab-separated columns: rsid / chromosome / position / genotype (AA · AG · GG). Preserves standard 23andMe raw-data format.

CSV / TSV

.csv .tsv

Required column: rsid. Optional: genotype (AA/AG/GG), carrier_state (heterozygous/homozygous_risk), chrom, pos, ref, alt.