Variants linked to Cognitive Decline Rate in Late MCI

Continuously updated · newest added Oct 21, 2026

13 positions on this site are linked to Cognitive Decline Rate in Late MCI, out of 103,694 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 Cognitive Decline Rate in Late MCI

Standard

Cognitive decline rate in late mild cognitive impairment

TSNARE1 · rs147368169

See detailed info →
Standard

Cognitive decline rate in late mild cognitive impairment

YWHAZ · rs116237496

See detailed info →
Standard

Cognitive decline rate in late mild cognitive impairment

IFNGR1 · rs117070989

See detailed info →
Standard

Cognitive decline rate in late mild cognitive impairment

TSNARE1 · rs145959269

See detailed info →
Standard

Cognitive decline rate in late mild cognitive impairment

SNHG5 · rs140295727

See detailed info →
Standard

Cognitive decline rate in late mild cognitive impairment

ADAM29 · rs183819925

See detailed info →
Standard

Cognitive decline rate in late mild cognitive impairment

FMO4 · rs116065238

See detailed info →
Standard

Cognitive decline rate in late mild cognitive impairment

CADPS · rs79158673

See detailed info →
Standard

Cognitive decline rate in late mild cognitive impairment

RBFOX1 · rs75638798

See detailed info →
Standard

Cognitive decline rate in late mild cognitive impairment

GNAI1 · rs799979

See detailed info →
Standard

Cognitive decline rate in late mild cognitive impairment

MYT1L · rs7581969

See detailed info →
Standard

Cognitive decline rate in late mild cognitive impairment

EIF4G3 · rs78649275

See detailed info →
Standard

Cognitive decline rate in late mild cognitive impairment

ADAM29 · rs76744071

See detailed info →

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.