rs1544410
NM_000376.3(VDR):c.1024+283G>A
- PeriodontitisBenign · germline
- Hepatocellular carcinoma (HCC)Likely risk allele · germline
- not providedBenign · ★ · germline
gnomAD allele frequency 3.39e-1
rs1544410 is a genetic variant located in the VDR gene. dbsnp · gene
In gnomAD, rs1544410 has an overall allele frequency of 33.9%. gnomad · frequency
In ClinVar, rs1544410 is classified as Benign for Periodontitis (0 review stars, germline; last evaluated 2023-04-20). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1544410 is classified as Likely risk allele (risk factor) for Hepatocellular carcinoma (HCC) (0 review stars, germline; last evaluated 2022-07-14). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1544410 is classified as Benign for not provided (1 review star, germline; last evaluated 2019-03-29). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
retrieved 2026-08-03 · facts 8f0f0d1ecc64e94b · 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.