rs1800497
NM_178510.2(ANKK1):c.2137G>A (p.Glu713Lys)
- Schizophrenia (SCZD)Benign · ★ · germline
- ANKK1-related disorderLikely benign · germline
- Taq1A POLYMORPHISMBenign · germline
- not specifiedBenign · ★ · germline
- not providedBenign · ★ · germline
gnomAD allele frequency 2.57e-1
rs1800497 is a genetic variant located in the ANKK1 gene. dbsnp · gene
In gnomAD, rs1800497 has an overall allele frequency of 25.7%. gnomad · frequency
In ClinVar, rs1800497 is classified as Benign for Schizophrenia (SCZD) (1 review star, germline). clinvar · classificationclinvar · review confidenceclinvar · origin
In ClinVar, rs1800497 is classified as Likely benign for ANKK1-related disorder (0 review stars, germline; last evaluated 2021-07-22). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1800497 is classified as Benign for Taq1A POLYMORPHISM (0 review stars, germline; last evaluated 2008-10-17). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1800497 is classified as Benign for not specified (1 review star, germline; last evaluated 2013-04-16). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1800497 is classified as Benign for not provided (1 review star, germline). clinvar · classificationclinvar · review confidenceclinvar · origin
retrieved 2026-08-03 · facts 5113da9afa9bdc67 · 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.