Links from this page to related variants, conditions, drugs and topics are not included for automated readers. Those connections are the Gene Knowledge Graph and are licensed as data: https://www.mygenelog.com/license
657 positions on this site are linked to Thyroid Cancer, out of 2,499,937 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
Strength of the evidence: all 2+ 3+ 4 Connections: all only those linked to a condition, drug or sense
PHKA1 · rs782062618
See detailed info → SensitivePHEX · rs760870713
See detailed info → SensitiveHRAS · rs28933406
See detailed info → SensitivePHEX · rs1057520582
See detailed info → SensitiveFAS · rs886039359
See detailed info → SensitiveFHL1 · rs886044238
See detailed info → SensitiveCOL4A5 · rs1057522042
See detailed info → SensitiveRS1 · rs281865340
See detailed info → SensitiveUROD · rs567894083
See detailed info → SensitiveNRAS · rs11554290
See detailed info → SensitivePHEX · rs1057517789
See detailed info → SensitiveRINT1 · rs200989342
See detailed info → SensitiveCOX15 · rs777659902
See detailed info → SensitiveENG · rs997074986
See detailed info → SensitiveCOL7A1 · rs2107799999
See detailed info → SensitiveRAI1 · rs757309140
See detailed info → SensitiveNRG1 · rs4733129
See detailed info → Sensitivenear BRMS1L · rs12589124
See detailed info → SensitiveTERT · rs7726159
See detailed info → Sensitivenear BRMS1L · rs2183451
See detailed info →Showing 20 of 657 · page 1 of 33
One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.
The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.
No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.
Yes — the search box above matches gene symbols and rsIDs as well as trait names.