Admin | Megan Judge Genetics

Gene	Full Name	Group / Disease

Add Variant / SNP

rsID

Alleles (e.g. CT)

Diseases

Gene	rsID	Alleles		RR	Pop	Schlr	Diseases	Group

Add Curated Study

Gene

rsID (optional)

Study Snippet

Authors

Year

Title

URL

PID

Bulk Import from ResearchRabbit CSV

CSV File

Gene — rsID

Title	Authors	Year	Link

Discover New Studies (Brave Search)

Searches the open web for a single SNP, then hides anything that's already filed under any gene/rsID or that you've previously marked Duplicate/Trash here — so what's left below is genuinely new to you.

Gene — rsID

Scholar Page Parser

Browse Google Scholar yourself for a SNP, then on the results page: right-click → View Page Source (or Ctrl/Cmd+U) — not the visible page itself, which loses the links — select all, copy, and paste the HTML below. Everything happens locally in your browser; nothing is fetched automatically, so there's no blocking risk.

Gene — rsID

Detected Page

Scholar Search

Pasted Page Source

Add Topic Group

Group Name Description

Group	Description

Add Disease

Disease Name Description SNPs

Disease	Description		SNPs

Export Gene Data as CSV

Gene

Backfill Missing Data from NCBI

Loops through every gene / SNP and fetches fresh data from NCBI, filling in anything that's missing. Run Backfill Genes first (adds maplocation), then one of the SNP options below. Backfill SNPs re-checks every SNP against NCBI regardless of current state (NCBI's own data changes over time) — run this every few months. Backfill Missing SNPs only touches SNPs missing a core field (chromosome/position/alleles/consequence) or with no population data at all — much faster, safe to run any time. Fix ClinVar + SNPedia only checks and stores those two flags (skips the slow NCBI variation fetch entirely) — fast enough to run across everything, anytime. Each NCBI request is throttled and retried on failure, so actual time is closer to 1–3 s per item than a flat rate.