ABCG1 p.Thr61=
c.183G>A · rs763046609 · VCV3046123
Likely benign
No assertion criteria
Classification
Likely benign
ClinVar
Review
No assertion criteria ☆☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
ultra-rare (popmax 0.011%, nfe)
Conditions
1
ABCG1-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 -10 | GERP -3.6 |
| Overall | ||
| CADD | 0.078 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.011%
European (non-Finnish) · 130/1,179,996 alleles
Filtering AF
0.00944%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 0.00888%
Overall
0.00898%
145/1,613,816 alleles · ultra-rare
| Ancestry group | Frequency | 1 in |
|---|---|---|
| European (non-Finnish)grpmax | 0.011% | 9,077 |
| South Asian | 0.00879% | 11,382 |
| Remaining individualsnot grpmax-eligible | 0.008% | 12,496 |
| East Asian | 0.00223% | 44,874 |
| African / African-American | 0.00134% | 74,844 |
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
- ABCG1
- Protein
- p.Thr61=
- Coding
- c.183G>A
- MANE Select
- NM_016818
- dbSNP
- rs763046609
- Type
- single nucleotide variant
- Location
- chr21:42225811 (GRCh38)
- Gene constraint
- LOEUF 0.573 · pLI 0.20 (gnomAD)
- Structure
- AlphaFold pLDDT 81.34 · 5 PDB
Disease context
ABCG1-related disorder
Similar variants
- ABCG1 p.Phe640Leu Uncertain significance ⚠ same condition
- ABCG1 c.538-6C>T Benign same condition
- ABCG1 p.Ala203= Likely benign same condition
- ABCG1 p.Asp614= Likely benign same condition
- ABCG1 p.Cys3= Benign same condition
- ABCG1 p.Gly331= Benign same condition
- ABCG1 p.Gly358Arg Benign same condition
- ABCG1 p.Leu113= 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/abcg1-p-thr61 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown