RS121908338 LDB3

Health Risk Chr 10:86687072 snv missense variant
Upload your DNA to see your genotype for this variant.
What This Variant Does
"rs121908338, also known as c.349G&gt
Associated Conditions
Population Frequencies
gnomAD ALL
99.7%
1kG AFR
2.3%
1kG ALL
99.2%
1kG AMR
99.4%
1kG EAS
100%
1kG EUR
99.6%
1kG SAS
0.1%
Other Variants in LDB3
Ask Dr. Hemsworth about this variant