RS9849237 CNTN4

Health Risk Chr 3:2633504 snv intron variant
Upload your DNA to see your genotype for this variant.
Associated Conditions
Population Frequencies
1kG AFR
53.8%
1kG ALL
26.3%
1kG AMR
30%
1kG EAS
9.6%
1kG EUR
18%
1kG SAS
22.6%
Other Variants in CNTN4
Ask Dr. Hemsworth about this variant