rs11045819
NM_006446.5(SLCO1B1):c.463C>A (p.Pro155Thr)
- Rotor syndrome (HBLRR)Benign · ★★ · germline
- SLCO1B1-related disorderLikely benign · germline
- not providedBenign · ★ · germline
- not specifiedBenign · germline
gnomAD allele frequency 1.11e-1
rs11045819 is a genetic variant located in the SLCO1B1 gene. dbsnp · gene
In gnomAD, rs11045819 has an overall allele frequency of 11.1%. gnomad · frequency
In ClinVar, rs11045819 is classified as Benign for Rotor syndrome (HBLRR) (2 review stars, germline; last evaluated 2024-11-29). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs11045819 is classified as Likely benign for SLCO1B1-related disorder (0 review stars, germline; last evaluated 2021-07-21). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs11045819 is classified as Benign for not provided (1 review star, germline). clinvar · classificationclinvar · review confidenceclinvar · origin
In ClinVar, rs11045819 is classified as Benign for not specified (0 review stars, germline). clinvar · classificationclinvar · review confidenceclinvar · origin
retrieved 2026-08-03 · facts e43b41da14bef50b · meta/llama-3.1-8b-instruct · prompt 4.0.1 · schema 3.0.0
Educational information only — not medical advice, a diagnosis, or a clinical interpretation. A variant's significance can be uncertain, conflicting, or dependent on your full clinical and family context. Consult a qualified genetics professional or genetic counselor before drawing any conclusion.