HMGN2P18 - KRTCAP2 HMGN2P18 - KRTCAP2
HMGN2P18 - KRTCAP2 (HMGN2P18 - KRTCAP2): 9 variants described, covering health risk, trait, nutrition.
Which HMGN2P18 - KRTCAP2 variants does Orviva describe?
- rs6676150 Health risk imported
- C allele associated with increased Calcium levels (UKB data field 30680) (β=0.024). [GWAS Catalog]
- rs75925257 Health risk imported
- G allele associated with increased Body mass index (β=0.019). [GWAS Catalog]
7 further HMGN2P18 - KRTCAP2 variants in the knowledge base have only a brief annotation and are not listed here.
See your own HMGN2P18 - KRTCAP2 genotypes
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What do my HMGN2P18 - KRTCAP2 variants say about me?”
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What do my HMGN2P18 - KRTCAP2 variants say about me?”
Genetic associations describe risk across populations, not a diagnosis for any one person. Most variants shift risk modestly and act alongside lifestyle, environment and other genes. Consumer DNA chips do not read every position and can be wrong at any single one. For general education only; talk to a clinician or genetic counsellor before acting on anything here, and never change a prescribed medicine without your prescriber.