rs1801725
rs1801725 is a multiallelic missense variant in CASR. On the GRCh38 forward strand, G is the reference allele and the reviewed common comparison is G/T. The T allele encodes Ser986 and is linked to about 0.05 to 0.08 mg/dL higher total serum calcium per copy on average. The studies do not establish that this amino-acid change itself reduces receptor activity or is the causal variant. Calls containing the unstudied A allele are outside the reviewed map.
Traits rs1801725 reads
Gene
Reference databases
How Biome reads this
Biome's whole-genome test reads this from one saliva sample, alongside all 3.2 billion letters of your DNA.
Biome DNA test →This page is for educational purposes only and is not medical advice. It is not intended to diagnose, treat, cure, or prevent any disease. Genetic results describe tendencies and predispositions, not diagnoses. Always consult a licensed clinician before making decisions about your health, medications, or supplements.