Hello,

I am new to the analysis of human genomic mutations and have identified a series of gene loci of interest, including variant positions and types (eg: chr1 10001 A C). I am now looking to associate these data with published databases related to gene loci diseases or phenotypes (eg: GWAS). My aim is to annotate these loci as comprehensively as possible using these databases.

Could you please suggest some databases resources that I could use for this purpose? Are there any user-friendly tools that could assist me with this task?

Any guidance would be greatly appreciated. Thank you in advance.