Is AR p.Asp732= (c.2196C>T) pathogenic?

AR p.Asp732= (c.2196C>T) is classified Benign in AR (ClinVar, Single submitter, 1 submitter; last evaluated 2023-09-28). Ultra-rare (popmax 0.0177%, eas); Associated with Kennedy disease.

What condition is associated with AR p.Asp732= (c.2196C>T)?

AR p.Asp732= (c.2196C>T) is associated with Kennedy disease, androgen insensitivity syndrome (ClinVar).

How common is AR p.Asp732= (c.2196C>T) in the general population?

AR p.Asp732= (c.2196C>T) is ultra-rare (popmax 0.0177%, eas) (gnomAD).

How is Kennedy disease inherited?

Typically X-linked recessive (Orphanet). A genetic counselor can assess individual risk for a family.

AR p.Asp732=

c.2196C>T · rs199940567 · VCV2925892

Benign Single submitter

Classification

Benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Rare

ultra-rare (popmax 0.0177%, eas)

Conditions

Kennedy disease

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 -4.5	GERP -3.7
Overall
CADD	0.734	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.0177% East Asian · 6/33,811 alleles

Filtering AF 0.00765% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00526%

Overall 0.00237% 26/1,097,996 alleles · ultra-rare

Ancestry group	Frequency	1 in
East Asiangrpmax	0.0177%	5,635
Admixed American	0.00217%	46,102
Remaining individualsnot grpmax-eligible	0.0021%	47,634
European (non-Finnish)	0.00201%	49,749

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.Asp732=
Coding: c.2196C>T
MANE Select: NM_000044
dbSNP: rs199940567
Type: single nucleotide variant
Location: chrX:67717500 (GRCh38)
Structure: AlphaFold pLDDT 58.85 · 95 PDB
Residue 732: the nr lbd domain; the 'interaction with ccar1' region; the 'interaction with kat7' region; an α-helix; the 'interaction with lpxn' region

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

Disease context

Kennedy disease — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Also linked: androgen insensitivity syndrome

For Kennedy disease (Orphanet):

Inheritance: X-linked recessive
Onset: Adult
Prevalence: <1 / 1 000 000 (Italy)

Similar variants

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
AR p.Ala871Val Pathogenic/Likely 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-asp732 (accessed [today's date]).

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