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Test details
Test · Diagnostics

FISH: Prader Willi Syndrome / SNRPN

Free home sample collection, physician reviewed10–14 DaysReports inBloodSample

This FISH test uses a fluorescent probe targeting the SNRPN gene within the 15q11–q13 region. A missing signal indicates a deletion of this region, which is consistent with Prader-Willi Syndrome, especially in cases due to paternal microdeletion (seen in ~70% of PWS patients).

₹7,000—Members pay ₹6300