Variants linked to Birth Weight

Continuously updated · newest added Sep 13, 2026

35 positions on this site are linked to Birth Weight, out of 8,459 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 Birth Weight

Standard

Offspring birth weight

GCK · rs2971669

See detailed info →
Standard

Birth weight

DTL · rs61830764

See detailed info →
Standard

Birth weight

KREMEN1 · rs134594

See detailed info →
Standard

Birth weight

TRIB1 · rs6989280

See detailed info →
Standard

Birth weight

NRIP1 · rs2229742

See detailed info →
Standard

Birth weight

RB1 · rs2854355

See detailed info →
Standard

Birth weight

FES · rs12906125

See detailed info →
Standard

Birth weight

PTH1R · rs2242116

See detailed info →
Standard

Birth weight

MLXIPL · rs62466330

See detailed info →
Standard

Birth weight

STRBP · rs700059

See detailed info →
Standard

Birth weight

ADCY5 · rs11719201

See detailed info →
Standard

Birth weight

WNT4 · rs2473248

See detailed info →
Standard

Birth weight

CCNL1 · rs13322435

See detailed info →
Standard

Birth weight

INS · rs72851023

See detailed info →
Standard

Birth weight

CDKAL1 · rs35261542

See detailed info →
Standard

Birth weight

PTCH1 · rs28510415

See detailed info →
Standard

Birth weight

MAFB · rs6016377

See detailed info →
Standard

Birth weight

ZBTB7B · rs3753639

See detailed info →
Standard

Birth weight

MIR2392 · rs6575803

See detailed info →
Standard

Birth weight

SPRED1 · rs75844534

See detailed info →

Showing 20 of 35 · page 1 of 2

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.