Is PRRC2A p.Val792= (c.2376A>G) pathogenic?

PRRC2A p.Val792= (c.2376A>G) is classified Benign in PRRC2A (ClinVar, No assertion criteria, 1 submitter; last evaluated 2019-10-21). Common (popmax 20.3%, afr) — too common for a highly-penetrant pathogenic allele; Associated with PRRC2A-related disorder.

What condition is associated with PRRC2A p.Val792= (c.2376A>G)?

PRRC2A p.Val792= (c.2376A>G) is associated with PRRC2A-related disorder (ClinVar).

PRRC2A p.Val792=

Q: How common is PRRC2A p.Val792= (c.2376A>G) in the general population?

PRRC2A p.Val792= (c.2376A>G) is common (popmax 20.3%, afr) — too common for a highly-penetrant pathogenic allele (gnomAD).

c.2376A>G · rs3130626 · VCV3059728

Benign No assertion criteria

Classification

Benign

ClinVar

Review

No assertion criteria ☆☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Common

common (popmax 20.3%, afr) — too common for a highly-penetrant pathogenic allele

Conditions

PRRC2A-related disorder

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 1.1	GERP -3.1, phastCons 1
Overall
CADD	7.088	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 20.3% African / African-American · 14,919/73,344 alleles

Filtering AF 20.1% ClinGen BA1/BS1 input FAF95, joint · FAF99 20%

Overall 17.6% 283,262/1,612,116 alleles · common exomes 257,607/1,460,932 · genomes 25,655/151,184 · joint denominator

Ancestry group	Frequency	1 in
African / African-Americangrpmax	20.3%	5
European (non-Finnish)	19.1%	5
Amishnot grpmax-eligible	17.4%	6
Remaining individualsnot grpmax-eligible	16.5%	6
Finnishnot grpmax-eligible	16%	6
Ashkenazi Jewishnot grpmax-eligible	11.9%	8
South Asian	11.5%	9
Middle Eastern	9.59%	10
Admixed American	8.52%	12
East Asian	5.03%	20

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: PRRC2A
Protein: p.Val792=
Coding: c.2376A>G
MANE Select: NM_004638
dbSNP: rs3130626
Type: single nucleotide variant
Location: chr6:31630712 (GRCh38)
Gene constraint: LOEUF 0.322 · pLI 1.00 (gnomAD)
Structure: AlphaFold pLDDT 40.07
Residue 792: the '4 x 57 aa type a repeats' region; the 'disordered' region

Full PRRC2A gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

PRRC2A-related disorder

Similar variants

PRRC2A p.Lys308Arg Uncertain significance ⚠ same condition
PRRC2A c.391-6C>A Likely benign same condition
PRRC2A c.4720-6C>G Likely benign same condition
PRRC2A c.5624+9C>T Benign same condition
PRRC2A c.760-10C>G Likely benign same condition
PRRC2A c.*9C>T Likely benign same condition
PRRC2A p.Ala1222= Likely benign same condition
PRRC2A p.Ala1283Thr Benign 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/prrc2a-p-val792 (accessed [today's date]).

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