35 positions on this site are linked to Vitamin D Deficiency and the GC Gene, out of 103,526 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
BTG3 · rs73195003
See detailed info → StandardHS1BP3 · rs62122090
See detailed info → Standardnear UGT2B7 · rs6600893
See detailed info → StandardNADSYN1 · rs4944958
See detailed info → Standardnear SFRP1 · rs867934853
See detailed info → StandardNT5C2 · rs1454700296
See detailed info → StandardSLC25A37 · rs952825245
See detailed info → StandardPXK · rs563431181
See detailed info → StandardRDH13 · rs1268647997
See detailed info → StandardLAMA2 · rs73776179
See detailed info → Standardnear ATP2B1 · rs150425221
See detailed info → Standardnear GPCPD1 · rs143313202
See detailed info → StandardGC · rs17767445
See detailed info → StandardGC · rs13107347
See detailed info → StandardANO6/ARID2 · rs719700
See detailed info → StandardGC · rs1526692
See detailed info → StandardHTR2A · rs1410656
See detailed info → StandardAMDHD1 · rs10745742
See detailed info → StandardCYP2R1 · rs117913124
See detailed info → StandardNADSYN1 · rs4423214
See detailed info →Showing 20 of 35 · page 1 of 2
One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.
The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.
No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.
Yes — the search box above matches gene symbols and rsIDs as well as trait names.