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

Sensitive

Skin cancer

JAZF1 · rs182533474

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Sensitive

Non-melanoma skin cancer

ZFHX4 · rs17431641

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Sensitive

Non-melanoma skin cancer

BPIFB4 · rs2424952

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Sensitive

Non-melanoma skin cancer

MC1R · rs12925026

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Sensitive

Non-melanoma skin cancer

near TRAK2 · rs10202963

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Sensitive

Non-melanoma skin cancer

DNAH2 · rs138420351

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Sensitive

Non-melanoma skin cancer

ZNF341 · rs111930714

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Sensitive

Non-melanoma skin cancer

FAM49A · rs16982256

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Standard

Low tan response

near DEF8 · rs4785752

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Standard

Low tan response

VPS9D1 · rs57119673

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Standard

Low tan response

ANKRD11 · rs55637757

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Standard

Low tan response

GRM5 · rs4121827

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Standard

Low tan response

RNF166 · rs75410747

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Standard

Low tan response

near KITLG · rs2639099

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Standard

Low tan response

near SLC24A4 · rs1885194

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Standard

Low tan response

near CDH15 · rs117156175

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Sensitive

Non-melanoma skin cancer

THNSL2 · rs6709352

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Standard

Low tan response

EXOC2 · rs71550013

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Standard

Low tan response

near SMIM38 · rs72932540

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Standard

Low tan response

DBNDD1 · rs77733403

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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.