VariantCheck

Zoekn

In-app purchases

About this app

VariantCheck is an informational research-reference tool for looking up how common a genetic variant is in the general population.

Search by gene, variant, rsID, or genomic coordinates (for example "APOE c.388T>C", "rs429358", or "19-44908684-T-C") and see population frequency data from gnomAD, the Genome Aggregation Database.

WHAT YOU CAN DO
• Search a gene, variant, rsID, or genomic coordinates
• View allele frequency data from gnomAD
• Automatically use the canonical (MANE Select) transcript when none is given
• Generate a written report of your search as a one-time in-app purchase

HOW IT WORKS
Create a free account, run as many searches as you like, and buy a report only when you want one. There are no subscriptions.

IMPORTANT
VariantCheck is an informational tool, not a medical service. It does not diagnose, treat, screen for, or monitor any medical condition. It does not provide medical advice, risk scores, or treatment recommendations. It does not offer genetic testing or sample processing. Talk to a qualified healthcare professional or genetic counselor about any health decision.

Data source: gnomAD (Genome Aggregation Database), a public resource of the Broad Institute. VariantCheck is not affiliated with or endorsed by gnomAD or the Broad Institute.

Privacy Policy: https://variant-check.com/privacy
Terms of Service: https://variant-check.com/terms