RS16881446 HS3ST1

Health Risk Chr 4:11406960 snv intron variant
Upload your DNA to see your genotype for this variant.
Associated Conditions
Population Frequencies
1kG AFR
69.9%
1kG ALL
26.4%
1kG AMR
22.2%
1kG EAS
81.7%
1kG EUR
25.7%
1kG SAS
66.5%
Ask Dr. Hemsworth about this variant