Variants linked to Basal Cell Carcinoma

Continuously updated · newest added Oct 25, 2026

146 positions on this site are linked to Basal Cell Carcinoma, out of 118,864 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 Basal Cell Carcinoma

Sensitive

Basal cell carcinoma

near LINC02889 · rs77890471

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Sensitive

Basal cell carcinoma

PTCSC2 · rs2805831

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Sensitive

Basal cell carcinoma

PTPN14 · rs6700380

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Sensitive

Basal cell carcinoma

JDP2 · rs7145468

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Sensitive

Basal cell carcinoma (PheCode 172.21)

near RNU6ATAC37P · rs79188822

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Sensitive

Basal cell carcinoma

near BCAS4 · rs62202836

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Sensitive

Basal cell carcinoma (PheCode 172.21)

HLA-DRB9 · rs9269080

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Sensitive

Basal cell carcinoma (MTAG)

TIPARP-AS1 · rs9878566

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Sensitive

Basal cell carcinoma

near CTLA4 · rs231729

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Sensitive

Basal cell carcinoma

near CTLA4 · rs1427676

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Sensitive

Basal cell carcinoma

near GACAT3 · rs16982253

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Sensitive

Basal cell carcinoma

RGS22 · rs28765982

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Sensitive

Basal cell carcinoma (MTAG)

GAS8 · rs7498985

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Sensitive

Basal cell carcinoma

P4HA2 · rs4705928

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Sensitive

Basal cell carcinoma

near XCL2 · rs78663305

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Sensitive

Basal cell carcinoma

IRF4 · rs142388808

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Sensitive

Basal cell carcinoma

FOXP1 · rs35768603

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Sensitive

Basal cell carcinoma

STRN · rs3845780

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Sensitive

Basal cell carcinoma

OSMR-DT · rs11743151

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Sensitive

Basal cell carcinoma

SSPN-AS1 · rs9668178

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Showing 20 of 146 · page 4 of 8

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.