Variants linked to Obesity and Body Weight

Continuously updated · newest added Oct 21, 2026

1,574 positions on this site are linked to Obesity and Body Weight, out of 104,660 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

← Back to Obesity and Body Weight

Standard

Body mass index

TENM2 · rs1013017

See detailed info →
Standard

Body mass index

near TSKU · rs7942337

See detailed info →
Standard

Body mass index

AGAP3 · rs749319

See detailed info →
Standard

Body mass index

ADAMTS9-AS2 · rs4688219

See detailed info →
Standard

Body mass index

FTO · rs185004749

See detailed info →
Standard

Body mass index

near ASH1L · rs151026328

See detailed info →
Standard

Body mass index

SYT14 · rs12136540

See detailed info →
Standard

Body mass index

near MC4R · rs11663643

See detailed info →
Standard

Body mass index

near LINC01915 · rs11083092

See detailed info →
Standard

Body mass index

SGMS1 · rs10763587

See detailed info →
Standard

Body mass index

NEBL · rs76638898

See detailed info →
Standard

Body mass index

LYPD1 · rs72844740

See detailed info →
Standard

Body mass index

near IQGAP3 · rs6685228

See detailed info →
Standard

Body mass index

SCN1A · rs51195

See detailed info →
Standard

Body mass index

HSD17B12 · rs12801812

See detailed info →
Standard

Body mass index

CACNB2 · rs1277733

See detailed info →
Standard

Body mass index

CWC27 · rs9291822

See detailed info →
Standard

Body mass index

DTNB · rs77931950

See detailed info →
Standard

Body mass index

LSAMP · rs6808814

See detailed info →
Standard

Body mass index

POLK · rs5744632

See detailed info →

Showing 20 of 1574 · page 10 of 79

Questions about variants on this site

What is a "variant" page on this site?

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.

Where does new variant data come from?

The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.

Does being listed here mean a variant causes a condition?

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.

Can I search this list by gene or rsID?

Yes — the search box above matches gene symbols and rsIDs as well as trait names.