Is ABCG5 p.Arg61= (c.183G>C) pathogenic?

ABCG5 p.Arg61= (c.183G>C) is classified Likely benign in ABCG5 (ClinVar, Single submitter, 1 submitter; last evaluated 2021-06-12). Absent from gnomAD v4.1; Associated with Cardiovascular phenotype.

What condition is associated with ABCG5 p.Arg61= (c.183G>C)?

ABCG5 p.Arg61= (c.183G>C) is associated with Cardiovascular phenotype (ClinVar).

How common is ABCG5 p.Arg61= (c.183G>C) in the general population?

ABCG5 p.Arg61= (c.183G>C) is absent from gnomAD v4.1 (gnomAD).

ABCG5 p.Arg61=

c.183G>C · rs2466141252 · VCV1781134

Likely benign Single submitter

Classification

Likely benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Absent

absent from gnomAD v4.1

Conditions

Cardiovascular phenotype

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 0.23	GERP -0.33, phastCons 0.01
Overall
CADD	5.054	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Absent from gnomAD v4.1. Not observed in any sequenced alleles — a rarity signal (ACMG PM2-supporting), not evidence of pathogenicity on its own.

Variant & gene context

Gene: ABCG5
Protein: p.Arg61=
Coding: c.183G>C
MANE Select: NM_022436
dbSNP: rs2466141252
Type: single nucleotide variant
Location: chr2:43837916 (GRCh38)
Gene constraint: LOEUF 1.219 · pLI <0.01 · ClinGen HI gene assoc. with recessive phenotype (gnomAD)
Structure: AlphaFold pLDDT 85.48 · 8 PDB
Residue 61: the abc transporter domain

Full ABCG5 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

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

Similar variants

ABCG5 p.Arg61Trp Uncertain significance ★★ ⚠ same residue
ABCG5 p.Arg61Gln Conflicting classifications of pathogenicity ★ ⚠ same residue
ABCG5 c.1325-1G>T Likely pathogenic ★★ same condition
ABCG5 p.Gln251Ter Pathogenic ★★ same condition
ABCG5 p.Glu146Ter Pathogenic ★★ same condition
ABCG5 p.Ala170Asp Uncertain significance ★★ ⚠ same condition
ABCG5 p.Ala264Val Uncertain significance ★★ ⚠ same condition
ABCG5 p.Ala278Glu Uncertain significance ★★ ⚠ 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/abcg5-p-arg61 (accessed [today's date]).

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