Variants linked to Cardiac Conduction Intervals (PR Interval and QRS Duration)

Continuously updated · newest added Oct 5, 2026

83 positions on this site are linked to Cardiac Conduction Intervals (PR Interval and QRS Duration), out of 41,275 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 Cardiac Conduction Intervals (PR Interval and QRS Duration)

Standard

PR interval

COL13A1 · rs2642608

See detailed info →
Standard

QRS duration

near PDHX · rs7113469

See detailed info →
Standard

PR interval

TBX20 · rs11763856

See detailed info →
Standard

QRS duration

NPAS2 · rs4851391

See detailed info →
Standard

PR interval

ARID2 · rs76611452

See detailed info →
Standard

PR interval

ADRB1 · rs67234920

See detailed info →
Standard

QRS duration

NOTCH2 · rs41302079

See detailed info →
Standard

PR interval

LPHN3 · rs28540500

See detailed info →
Standard

PR interval

FLRT2 · rs17712080

See detailed info →
Standard

PR interval

TMEM198 · rs13023533

See detailed info →
Standard

QRS duration

near MIR5702 · rs17195832

See detailed info →
Standard

QRS duration

PPARGC1A · rs73243622

See detailed info →
Standard

PR interval

CCBE1 · rs12961264

See detailed info →
Standard

PR interval

HCN4 · rs8039168

See detailed info →
Standard

QRS duration

PDLIM5 · rs12640669

See detailed info →
Standard

PR interval

DLC1 · rs1188285

See detailed info →
Standard

PR interval

TFEB · rs1015149

See detailed info →
Standard

PR interval

SDPR · rs58577564

See detailed info →
Standard

PR interval

PLPP7 · rs4584185

See detailed info →
Standard

PR interval

FGF18 · rs78810186

See detailed info →

Showing 20 of 83 · page 1 of 5

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.