Variants linked to Sun Sensitivity, Freckling and Skin Cancer Risk

Continuously updated · newest added Oct 21, 2026

70 positions on this site are linked to Sun Sensitivity, Freckling and Skin Cancer Risk, out of 102,854 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 Sun Sensitivity, Freckling and Skin Cancer Risk

Standard

Low tan response

near GRM5 · rs7937452

See detailed info →
Standard

Low tan response

TYRP1 · rs1326797

See detailed info →
Standard

Low tan response

DEF8 · rs3803686

See detailed info →
Standard

Low tan response

PDE4B · rs1308048

See detailed info →
Standard

Low tan response

TRPS1 · rs2737212

See detailed info →
Standard

Low tan response

OCA2 · rs1800407

See detailed info →
Standard

Low tan response

EMX2 · rs35563099

See detailed info →
Sensitive

Non-melanoma skin cancer

NCOA6 · rs62211621

See detailed info →
Sensitive

Non-melanoma skin cancer

near CHMP4B · rs62209647

See detailed info →
Standard

Low tan response

MROH8 · rs73094911

See detailed info →
Standard

Low tan response

SAMHD1 · rs11696169

See detailed info →
Standard

Low tan response

near SRC · rs11697428

See detailed info →
Standard

Low tan response

PRDM7 · rs117417690

See detailed info →
Standard

Low tan response

near KIF3B · rs77476644

See detailed info →
Standard

Low tan response

near PHF20 · rs112043138

See detailed info →
Standard

Low tan response

UQCC1 · rs62210588

See detailed info →
Standard

Low tan response

ZNF341 · rs78382342

See detailed info →
Standard

Low tan response

TM9SF4 · rs17093831

See detailed info →
Standard

Low tan response

SLA2 · rs55804368

See detailed info →
Standard

Low tan response

MTCL2 · rs73109224

See detailed info →

Showing 20 of 70 · page 3 of 4

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.