Is AR p.Val582= (c.1746C>T) pathogenic?

AR p.Val582= (c.1746C>T) is classified Benign/Likely benign in AR (ClinVar, Multiple submitters, 2 submitters; last evaluated 2024-01-27). Ultra-rare (popmax 0.0664%, afr); Associated with androgen insensitivity syndrome.

What condition is associated with AR p.Val582= (c.1746C>T)?

AR p.Val582= (c.1746C>T) is associated with androgen insensitivity syndrome, Kennedy disease (ClinVar).

How common is AR p.Val582= (c.1746C>T) in the general population?

AR p.Val582= (c.1746C>T) is ultra-rare (popmax 0.0664%, afr) (gnomAD).

AR p.Val582=

c.1746C>T · rs145171897 · VCV254735

Benign/Likely benign Multiple submitters

Classification

Benign/Likely benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 2 submitters

gnomAD v4.1

Rare

ultra-rare (popmax 0.0664%, afr)

Conditions

androgen insensitivity syndrome

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 0.24	GERP -0.7, phastCons 0.98
Overall
CADD	6.36	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.0664% African / African-American · 38/57,235 alleles

Filtering AF 0.0497% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.0439%

Overall 0.00364% 44/1,209,169 alleles · ultra-rare

Ancestry group	Frequency	1 in
African / African-Americangrpmax	0.0664%	1,506
Remaining individualsnot grpmax-eligible	0.00631%	15,849
Admixed American	0.00439%	22,770
European (non-Finnish)	0.000112%	894,839

Rarity supports pathogenicity (ACMG PM2); frequency above a disease-specific BA1/BS1 threshold argues against it. A variant frequent in one ancestry group can be near-absent in others, so a single global figure can mislead.

Variant & gene context

Gene: AR
Protein: p.Val582=
Coding: c.1746C>T
MANE Select: NM_000044
dbSNP: rs145171897
Type: single nucleotide variant
Location: chrX:67643385 (GRCh38)
Structure: AlphaFold pLDDT 58.85 · 95 PDB
Residue 582: the 'interaction with hipk3' region; a DNA-binding region; an α-helix; the 'interaction with znf318' region; a UniProt-annotated variant site (in ais); the 'interaction with lpxn' region

Full AR gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

androgen insensitivity syndrome — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Also linked: Kennedy disease

Similar variants

AR p.Val582Asp Uncertain significance ★ ⚠ same residue
AR c.1768+2T>C Pathogenic/Likely pathogenic ★★ same condition
AR c.1769-11T>A Pathogenic ★★ same condition
AR c.2450-6C>G Pathogenic ★★ same condition
AR p.Ala588Pro Pathogenic/Likely pathogenic ★★ same condition
AR p.Ala597Thr Pathogenic ★★ same condition
AR p.Ala688Val Pathogenic/Likely pathogenic ★★ same condition
AR p.Ala766Thr Pathogenic ★★ same condition

Built on 18 open, versioned datasets — ClinVar, gnomAD, AlphaMissense, REVEL, ClinGen & more — plus Sugi Variant's own cross-source analysis. Source data 2026-01–2026-10, ClinVar 2026-10. Full sources & versions →

Cite Sugi Variant

Gür T. Sugi Variant: A Deterministic Per-Variant Germline Reference from a Knowledge Graph for Humans and AI Agents. 2026. doi:10.5281/zenodo.21509445. This variant: https://sugi.bio/variant/ar-p-val582 (accessed [today's date]).

Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown